conceptofmind/minipile_embeddings_bf16 · Datasets at Hugging Face

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Essays Philosophers who think everyday morality is objective should examine the evidence, argues Joshua Knobe. Imagine two people discussing a question in mathematics. One of them says “7,497 is a prime number,” while the other says, “7,497 is not a prime number.” In a case like this one, we would probably conclude that there can only be a single right answer. We might have a lot of respect for both participants in the conversation, we might agree that they are both very reasonable and conscientious, but all the same, one of them has got to be wrong. The question under discussion here, we might say, is perfectly objective. But now suppose we switch to a different topic. Two people are talking about food. One of them says “Don’t even think about eating caterpillars! They are totally disgusting and not tasty at all,” while the other says “Caterpillars are a special delicacy – one of the tastiest, most delectable foods a person can ever have occasion to eat.” In this second case, we might have a very different reaction. We might think that there isn’t any single right answer. Maybe caterpillars are just tasty for some people but not for others. This latter question, we might think, should be understood as relative. Now that we’ve got at least a basic sense for these two categories, we can turn to a more controversial case. Suppose that the two people are talking about morality. One of them says “That action is deeply morally wrong,” while the other is speaking about the very same action and says “That action is completely fine – not the slightest thing to worry about.” In a case like this, one might wonder what reaction would be most appropriate. Should we say that there is a single right answer and anyone who says the opposite must be mistaken, or should we say that different answers could be right for different people? In other words, should we say that morality is something objective or something relative? This is a tricky question, and it can be difficult to see how one might even begin to address it. Faced with an issue like this one, where exactly should we look for evidence? Though philosophers have pursued numerous approaches here, one of the most important and influential is to begin with certain facts about people’s ordinary moral practices. The idea is that we can start out with facts about people’s usual ways of thinking or talking and use these facts to get some insight into questions about the true nature of morality. Thinkers who take this approach usually start out with the assumption that ordinary thought and talk about morality has an objectivist character. For example, the philosopher Michael Smith claims that we seem to think moral questions have correct answers; that the correct answers are made correct by objective moral facts; that moral facts are wholly determined by circumstances and that, by engaging in moral conversation and argument, we can discover what these objective moral facts determined by the circumstances are. And Frank Jackson writes: I take it that it is part of current folk morality that convergence will or would occur. We have some kind of commitment to the idea that moral disagreements can be resolved by sufficient critical reflection – which is why we bother to engage in moral debate. To that extent, some sort of objectivism is part of current folk morality. Then, once one has in hand this claim about people’s ordinary understanding, the aim is to use it as part of a complex argument for a broader philosophical conclusion. It is here that philosophical work on these issues really shines, with rigorous attention to conceptual distinctions and some truly ingenious arguments, objections and replies. There is just one snag. The trouble is that no real evidence is ever offered for the original assumption that ordinary moral thought and talk has this objective character. Instead, philosophers tend simply to assert that people’s ordinary practice is objectivist and then begin arguing from there. If we really want to go after these issues in a rigorous way, it seems that we should adopt a different approach. The first step is to engage in systematic empirical research to figure out how the ordinary practice actually works. Then, once we have the relevant data in hand, we can begin looking more deeply into the philosophical implications – secure in the knowledge that we are not just engaging in a philosophical fiction but rather looking into the philosophical implications of people’s actual practices. Just in the past few years, experimental philosophers have been gathering a wealth of new data on these issues, and we now have at least the first glimmerings of a real empirical research program here. But a funny thing happened when people started taking these questions into the lab. Again and again, when researchers took up these questions experimentally, they did not end up confirming the traditional view. They did not find that people overwhelmingly favoured objectivism. Instead, the results consistently point to a more complex picture. There seems to be a striking degree of conflict even in the intuitions of ordinary folks, with some people under some circumstances offering objectivist answers, while other people under other circumstances offer more relativist views. And that is not all. The experimental results seem to be giving us an ever deeper understanding of why it is that people are drawn in these different directions, what it is that makes some people move toward objectivism and others toward more relativist views. For a nice example from recent research, consider a study by Adam Feltz and Edward Cokely. They were interested in the relationship between belief in moral relativism and the personality trait openness to experience. Accordingly, they conducted a study in which they measured both openness to experience and belief in moral relativism. To get at people’s degree of openness to experience, they used a standard measure designed by researchers in personality psychology. To get at people’s agreement with moral relativism, they told participants about two characters – John and Fred – who held opposite opinions about whether some given act was morally bad. Participants were then asked whether one of these two characters had to be wrong (the objectivist answer) or whether it could be that neither of them was wrong (the relativist answer). What they found was a quite surprising result. It just wasn’t the case that participants overwhelmingly favoured the objectivist answer. Instead, people’s answers were correlated with their personality traits. The higher a participant was in openness to experience, the more likely that participant was to give a relativist answer. Geoffrey Goodwin and John Darley pursued a similar approach, this time looking at the relationship between people’s belief in moral relativism and their tendency to approach questions by considering a whole variety of possibilities. They proceeded by giving participants mathematical puzzles that could only be solved by looking at multiple different possibilities. Thus, participants who considered all these possibilities would tend to get these problems right, whereas those who failed to consider all the possibilities would tend to get the problems wrong. Now comes the surprising result: those participants who got these problems right were significantly more inclined to offer relativist answers than were those participants who got the problems wrong. Taking a slightly different approach, Shaun Nichols and Tricia Folds-Bennett looked at how people’s moral conceptions develop as they grow older. Research in developmental psychology has shown that as children grow up, they develop different understandings of the physical world, of numbers, of other people’s minds. So what about morality? Do people have a different understanding of morality when they are twenty years old than they do when they are only four years old? What the results revealed was a systematic developmental difference. Young children show a strong preference for objectivism, but as they grow older, they become more inclined to adopt relativist views. In other words, there appears to be a developmental shift toward increasing relativism as children mature. (In an exciting new twist on this approach, James Beebe and David Sackris have shown that this pattern eventually reverses, with middle-aged people showing less inclination toward relativism than college students do.) So there we have it. People are more inclined to be relativists when they score highly in openness to experience, when they have an especially good ability to consider multiple possibilities, when they have matured past childhood (but not when they get to be middle-aged). Looking at these various effects, my collaborators and I thought that it might be possible to offer a single unifying account that explained them all. Specifically, our thought was that people might be drawn to relativism to the extent that they open their minds to alternative perspectives. There could be all sorts of different factors that lead people to open their minds in this way (personality traits, cognitive dispositions, age), but regardless of the instigating factor, researchers seemed always to be finding the same basic effect. The more people have a capacity to truly engage with other perspectives, the more they seem to turn toward moral relativism. To really put this hypothesis to the test, Hagop Sarkissian, Jennifer Wright, John Park, David Tien and I teamed up to run a series of new studies. Our aim was to actually manipulate the degree to which people considered alternative perspectives. That is, we wanted to randomly assign people to different conditions in which they would end up thinking in different ways, so that we could then examine the impact of these different conditions on their intuitions about moral relativism. Participants in one condition got more or less the same sort of question used in earlier studies. They were asked to imagine that someone in the United States commits an act of infanticide. Then they were told to suppose that one person from their own college thought that this act was morally bad, while another thought that it was morally permissible. The question then was whether they would agree or disagree with the following statement: Since your classmate and Sam have different judgments about this case, at least one of them must be wrong. Participants in the other conditions received questions aimed at moving their thinking in a different direction. Those who had been assigned to the “other culture” condition were told to imagine an Amazonian tribe, the Mamilons, which had a very different way of life from our own. They were given a brief description of this tribe’s rituals, values and modes of thought. Then they were told to imagine that one of their classmates thought that the act of infanticide was morally bad, while someone from this Amazonian tribe thought that the act was morally permissible. These participants were then asked whether they agreed or disagreed with the corresponding statement: Since your classmate and the Mamilon have different judgments about this case, at least one of them must be wrong. Finally, participants in the “extraterrestrial” condition were told about a culture that was just about as different from our own as can possibly be conceived. They were asked to imagine a race of extraterrestrial beings, the Pentars, who have no interest in friendship, love or happiness. Instead, the Pentars’ only goal is to maximise the total number of equilateral pentagons in the universe, and they move through space doing everything in their power to achieve this goal. (If a Pentar becomes too old to work, she is immediately killed and transformed into a pentagon herself.) As you might guess, these participants were then told to imagine a Pentar who thinks that the act of infanticide is morally permissible. Then came the usual statement: Since your classmate and the Pentar have different judgments about this case, at least one of them must be wrong. The results of the study showed a systematic difference between conditions. In particular, as we moved toward more distant cultures, we found a steady shift toward more relativist answers – with people in the first condition tending to agree with the statement that at least one of them had to be wrong, people in the second being pretty evenly split between the two answers, and people in the third tending to reject the statement quite decisively. Note that all participants in the study are considering judgments about the very same act. There is just a single person, living in the United States, who is performing an act of infanticide, and participants are being asked to consider different judgments one might make about that very same act. Yet, when participants are asked to consider individuals who come at the issue from wildly different perspectives, they end up concluding that these individuals could have opposite opinions without either of them being in any way wrong. This result seems strongly to suggest that people can be drawn under certain circumstances to a form of moral relativism. But now we face a new question. If we learn that people’s ordinary practice is not an objectivist one – that it actually varies depending on the degree to which people take other perspectives into account – how can we then use this information to address the deeper philosophical issues about the true nature of morality? The answer here is in one way very complex and in another very simple. It is complex in that one can answer such questions only by making use of very sophisticated and subtle philosophical methods. Yet, at the same time, it is simple in that such methods have already been developed and are being continually refined and elaborated within the literature in analytic philosophy. The trick now is just to take these methods and apply them to working out the implications of an ordinary practice that actually exists. Share This Joshua Knobe is an associate professor at Yale University, affiliated both with the Program in Cognitive Science and the Department of Philosophy.	3.0625	3	[ 0.005615234375, 0.000274658203125, 0.01446533203125, -0.005767822265625, 0.0022735595703125, 0.000640869140625, 0.0172119140625, 0.001922607421875, -0.00555419921875, 0.031494140625, -0.00146484375, 0.01068115234375, -0.0162353515625, 0.01043701171875, -0.006988525390625, -0.00518798828125, -0.004974365234375, 0.00848388671875, 0.001708984375, 0.007781982421875, -0.036376953125, -0.0020294189453125, -0.00122833251953125, -0.00701904296875, -0.00139617919921875, -0.007476806640625, -0.004913330078125, 0.006256103515625, -0.0031890869140625, 0.0196533203125, 0.0128173828125, 0.0014495849609375, 0.000804901123046875, 0.0027008056640625, -0.0037384033203125, -0.0135498046875, -0.004058837890625, 0.01019287109375, 0.004058837890625, 0.001922607421875, 0.0072021484375, -0.00640869140625, -0.00311279296875, 0.00958251953125, 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Social Mining using R 1. 200 tweets are extracted from hashtag “#california” and 200 from hashtag “#newyork”. 2. Then create 2 corpus from the 2 datasets. 3. Preprocess the corpus using {tm} package from R. 4. Compute and display the most frequent terms (words) in each corpus. 5. Create 2 word clouds from the most frequent terms. 6. Compute the sentiment scores, i.e. determine whether words used in the tweets are more positively or negatively charged (emotionally). ![sentimentscores.png](/site_media/media/7d5429b20e891.png) ###Sentiment scores summary:### In general, tweets from both states have positive sentiments. However, it seem like tweets from #california appear to have a more negative connotation than #newyork. ## Facebook API ## 1. Consume 100 most recent Facebook posts by user “joebiden” using getPage() from R’s {RFacebook} package. a. Find the most liked post and it’s popularity. b. Find the most commented post and the number of comments. c. Create a word cloud based on the most popular words used in the most commented post. 2. Consume 100 most recent Facebook posts containing the word “petaluma” using searchPages(). a. 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-ase The suffix -ase is used in biochemistry to form names of enzymes. The most common way to name enzymes is to add this suffix onto the end of the substrate, e.g. an enzyme that breaks down peroxides may be called peroxidase; the enzyme that produces telomeres is called telomerase. Sometimes enzymes are named for the function they perform, rather than substrate, e.g. the enzyme that polymerizes (assembles) DNA into strands is called polymerase; see also reverse transcriptase. The commonly used -ase suffix for naming enzymes was derived from the name diastase. 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[/caption] Among one of the first exoplanet systems imaged was HR 8799. In 2008, a team led by Christian Marois at the Herzberg Institute of Astrophysics in Canada, took a picture of the system directly imaging three giant planets. The team revisited the system in 2009 – 2010 with the Keck II telescope and discovered a fourth planet in the system. The new planet, designated HR 8799e, orbits at a distance of 14.5 AU, making it the innermost planet in the system. The other planets all orbit at distances of >25 AU. The images were taken in the near infrared where they are most noticeable because the system is relatively young (<100 Myr) and the planets are still radiating large amounts of heat from their formation. The youth of these planets is part of what makes them an interesting target for astronomers. There exists a controversy in the community of planetary astronomers on the formation method of large planets. One theory states that planets form from a single, monolithic collapse that creates the entire planet’s mass at one time. Another possibility is that the initial collapse forms small cores early on, but then there is substantial growth later, as the planetesimal sweeps up additional material. The discovery of the new planet challenges both theories. Marois states, “none of [the theories] can explain the in situ formation of all four planets.” Thus, a combination of both methods may be in use in the system. Several belts of dust are also known in the system which may help astronomers determine what modes of formation were present. In particular HR 8799e is challenging to an in situ formation because the gravitational perturbations from the parent star should disrupt the formation of large gas planets within 20-40 AU from a single formation. Instead, the new planet would likely have had to been a core collapse with subsequent accretion, or alternatively, moved to its present location via migration. Studying systems such as this may help astronomers better understand the formation of our own solar system. The paper notes that the HR 8799 “does show interesting similarities with the Solar system with all giant planets located past the system’s estimated snow line (~2.7 AU for the Solar system and ~6 AU for HR 8799)”. Additionally, both have debris disks beyond the outer orbits with similar temperatures. Different methods of detecting planetary formation necessarily turn up different types of systems. Radial velocity studies detect massive, close-in planets whereas direct imaging most easily finds more distant planets. These two apparent populations represent different modes of planetary formation and for a full understanding, astronomers will need a continuous sampling that merges the two. Marois notes that we are still far from this goal as “[w]e just do not have enough exoplanets detected by direct imaging (~6 so far)” to make any conclusions besides constraints from the non-detections occurring thus far. To truly merge these two populations, astronomers will likely need to wait until more systems are discovered. Previously, some work has been done to estimate the composition of the atmospheres of the three planets already discovered in the system. These systems have been suggested to have cloudy atmospheres for CH 4 and CO. According to Marois, his team is, “planning more observations on e, but it will be hard. We might have to wait for new instruments, like the Gemini Planet Imager to do it properly.” This new instrument “will put a ‘thumb’ on the star (or what we call a coronagraph) to physically block the star light and allow ‘easy’ detection of nearby faint planets.” While this discovery is a first, it will certainly be one of a long line of exoplanet images. Marois is obviously excited about the ability to directly image planets. I asked him what the single most important thing he wanted readers to get from this research. His response was simple, “That we now have the telescopes and instruments to SEE planets orbiting other stars – that’s really cool! The exoplanet field is still very young and we have so much to learn.”	3.984375	4	[ -0.0120849609375, -0.0211181640625, -0.00726318359375, -0.01165771484375, 0.00213623046875, -0.015869140625, -0.0238037109375, 0.00188446044921875, 0.00335693359375, -0.02197265625, 0.01123046875, 0.00958251953125, -0.01483154296875, -0.00128173828125, -0.006866455078125, -0.00640869140625, -0.0037078857421875, 0.00390625, 0.0196533203125, 0.0179443359375, 0.0277099609375, 0.0032958984375, -0.014892578125, -0.006256103515625, 0.00933837890625, 0.00579833984375, -0.011962890625, -0.01214599609375, -0.0027923583984375, -0.0036773681640625, 0.01348876953125, 0.01251220703125, -0.033203125, -0.00701904296875, -0.004852294921875, -0.0013885498046875, 0.005767822265625, 0.0145263671875, -0.0103759765625, -0.03076171875, -0.00113677978515625, 0.01190185546875, -0.0025482177734375, 0.015869140625, 0.0120849609375, -0.0096435546875, 0.00567626953125, 0.016845703125, 0.00482177734375, 0.0089111328125, 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Astenois Astenois (Latin pagus Stadunensis) was a pagus, the most basic division of territory in the Roman and Frankish empires. In the Middle Ages, it comprised the parishes of the deaconries of Sainte-Menehould and Possesse. Originally a part of Lotharingia, by the eleventh century its southern part belonged to the Holy Roman Empire and its northern part to the Kingdom of France. The original seat of its counts was at Le Vieil-Dampierre. Traditionally, Astenois, Dormois and Castrice, the three eastern pagi of the archdiocese of Reims were held to belong to the empire. In the eleventh century, as part of a general fragmentation of power in the region, new counties were formed which did not correspond to ancient pagi but were instead named after their main castles. The county of Astenois, which did correspond to an old pagus, became known as the county of Dampierre after its rulers' chief fortress. The counts of Astenois were originally a cadet branch of the counts of Toul. The county was produced through the division of the patrimony of Frederick II. The elder son, Renard III, received Toul, while the younger, Peter, received Astenois. Astenois may originally have been a small fief of the bishops of Toul. It may have passed from the last count of the old line, Renard II, to the first count of the new, Frederick I, through the marriage of the latter to the former's daughter, Gertrude, at the same time as the bishop made Frederick count of Toul (1059). Frederick and Gertrude's son, Frederick II, then divided the patrimony for his sons. __NOTOC__ List of counts and lords Peter Frederick Henry Renard I Renard II Renard III Renard IV Anselm I Anselm II John I John II Notes Sources Further reading Category:Subdivisions of the Holy Roman Empire Category:Medieval France	3.328125	3	[ -0.004302978515625, 0.0031585693359375, 0.0011138916015625, 0.0230712890625, 0.021484375, -0.006256103515625, -0.006561279296875, 0.00115966796875, -0.006256103515625, -0.00787353515625, -0.0038299560546875, -0.007171630859375, -0.058349609375, -0.01153564453125, -0.0128173828125, -0.0140380859375, -0.0020294189453125, 0.002532958984375, 0.007415771484375, -0.00360107421875, -0.099609375, 0.0294189453125, 0.008056640625, 0.0126953125, 0.00408935546875, -0.005157470703125, 0.001983642578125, -0.000659942626953125, -0.0036468505859375, -0.00787353515625, 0.006561279296875, 0.00823974609375, -0.00872802734375, 0.01190185546875, 0.005767822265625, 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Operation IceBridge, NASA's airborne mission to monitor polar ice, is amid its fourth week of flights for the Arctic 2011 campaign. Researchers and crew successfully completed flights from Thule, Greenland, to monitor sea ice and have now moved to Kangerlussuaq, Greenland to focus on flights monitoring the ice sheet. Flying a distance of about 19,000 miles [30,000 kilometers] over the Arctic Ocean, scientists onboard the P-3 collected data during eight sea ice flights based from Thule Air Base. One additional sea ice flight remains to be flown from Kangerlussuaq. Why Fly Sea Ice? Sea ice flights, flown this year from March 16-28, take priority early in the mission's Arctic campaigns. That's because sea ice typically reaches its annual maximum extent in March, and scientists want to collect data before the ice begins to melt and retreat during northern hemisphere's summer. This year, sea ice reached its maximum extent on March 7, reaching 5.7 million square miles and tying for the lowest extent since the start of satellite measurements in 1979. The thickness of Arctic sea ice cover is also declining, on average, throughout the satellite record, according to scientists including Joey Comiso of NASA's Goddard Space Flight Center in Greenbelt, Md. Now, after the Ice, Cloud, and land Elevation Satellite (ICESat) stopped collecting data in 2009, IceBridge continues to collect the data scientists need to observe sea ice thickness. The mission's airborne instrument suite collects lidar and radar data making it possible to monitor both the sea ice freeboard and the snow layer on top of the sea ice. Both measurements are important for quantifying the sea ice thickness and predicting the heat exchange between the Arctic Ocean and the atmosphere. Then, on March 23, the P-3 flew one of the campaign's most challenging flights - an overpass of the U.S. Navy's ICEX camp, an assemblage of tents and shacks drifting on an ice floe north of Fairbanks. On the ground with ICEX was a team of researchers from the Army's Cold Regions Research and Engineering Laboratory and the Naval Research Laboratory, who established a line that would be surveyed from on, below and above the ice. Comparing measurements from each vantage point helps scientists improve the accuracy of sea ice thickness measurements. Sea ice camps are moving targets, drifting along with the wind and ocean currents. The erratic movement makes for a challenging overflight. "The sea ice moves unpredictably, crazy, like a drunken sailor," said John Sonntag of URS Corporation, and the IceBridge instrument team lead. Just before the mission, the camp was floating north at about 66 feet per hour, but by the time the aircraft was nearby it had suddenly veered east at about 660 feet per hour. The flyover required precise coordination with ground teams before and during the flight. The P-3 returned to Thule on March 25 to complete three more science flights before transiting to Kangerlussuaq, the base of operations for the next few weeks. Land Ho! The single remaining sea ice flight planned to fly from Kangerlussuaq will overfly a CRYOVEX site. The sites are designed to calibrate the European Space Agency's ice-observing satellite, CryoSat-2. Overflying the site will help scientist link the ICESat, IceBridge and Cryosat-2 datasets. Meanwhile, IceBridge scientists are working to complete a series of land ice flights. To date, IceBridge has completed four land ice flights over west Greenland. Weather has been favorable in that area, which is typical. Upcoming land ice missions to southeast Greenland will rely on a bit more luck, as low pressure from the Icelandic low commonly produces clouds in the region. Sand Drift ExplainedStavanger, Norway (SPX) Apr 11, 2011 The sand along the south-western coastal rim of Norway has drifted for more than 9000 calendar years. This was triggered by sea-level changes and human activities, new research has found. Researchers in countries such as Denmark, the Netherlands and Poland study sand drift, but most of them are focusing on sand dunes along the coastline, not on the plains further inland. "Sand dunes ... read more The content herein, unless otherwise known to be public domain, are Copyright 1995-2014 - Space Media Network. AFP, UPI and IANS news wire stories are copyright Agence France-Presse, United Press International and Indo-Asia News Service. ESA Portal Reports are copyright European Space Agency. All NASA sourced material is public domain. 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Several plant lectins are known as potent immunomodulatory agents, and they are applied in different experimental models of infection (Afonso-Cardoso et al., [@B1]; Oliveira et al., [@B13]). Recent research has characterized these proteins as potential agonists of Toll-like receptors (TLRs or TLR), a family of mammalian homologs of Drosophila Toll protein involved in the detection of microbes and initiating inflammatory responses (O\'Neill et al., [@B14]). In this opinion article, we highlighted some studies of plant lectins as modulators or agonists of TLRs in order to stimulate research interest in this fascinating area and promote knowledge sharing and scientific collaboration. A short view on plant lectins ============================= Lectins are a very large class of carbohydrate-binding proteins of non-immune origin. Through the interaction with sugars, they trigger several important cellular processes. Lectins are universally expressed and have been shown to function in animals, plants, and microorganisms as cell and molecular recognition proteins. However, the carbohydrate-binding domains have been studied most intensively within the plant kingdom (Sharon, [@B16]; Vandenborre et al., [@B20]). The discovery of plant lectins occurred in the 19th century, however, many questions about the biological role of these molecules remain obscure. Lectins may be involved in sugar transport, carbohydrate storage and they are associated as molecular chaperones (Van Damme et al., [@B18a]; Liu and Li, [@B10]). The adhesion and agglutination properties of lectins have been related in the interaction of both symbiotic and pathogenic interaction of some microorganisms and host (Audfray et al., [@B2]). Plant lectins represent a group of proteins with obvious differences in their biochemical/physicochemical properties, molecular structure, carbohydrate-binding specificity and biological activities (Liu et al., [@B9]). Lectins are oligomeric which exhibit a large structural diversity and the molecular size range from 60 to 400 kDa. Each lectin polypeptide contains many molecular domains, one of which is the non-catalytic carbohydrate recognition domain, responsible for their ability to recognize and interact with specific glycoconjugates, without altering their structure. In the past few years, hundreds of plant lectins have been purified and characterized in details with respect to their biochemical properties, carbohydrate-binding specificities, these approaches allowed their classification (Van Dammes et al., [@B19]). Toll-like receptors =================== Plant materials represent an excellent source of immune modulators, which have been appointed as a new approach for combating infections caused by resistant microorganisms (Hancock et al., [@B5]). In this sense, a range of potential compounds have been proposed as agonists or inductors of immune receptors, including TLRs. The TLR family is the best characterized group of innate immune receptors in terms of known ligands, downstream signaling pathways and functional relevance. They comprise a family of receptors homologous to Toll receptor from Drosophila melanogaster. In humans, the TLR family includes 10 transmembrane proteins that play a crucial role in host defense: they recognize molecular characteristics of microorganisms, known as pathogen-associated molecular patterns (PAMPs) highly conserved between different classes of microorganisms. For example, TLR4 and accessory proteins recognize lipopolysaccharide (LPS), while TLR2 recognizes lipoteichoic acid and various lipopeptides (when in complex with either TLR-1 or TLR-6), and TLR5 recognizes flagellin (Hancock et al., [@B5]; O\'Neill et al., [@B14]). In this way, TLR receptors represent important therapeutic targets for developing new drugs able to directly modulate the host response against microbial infection. In fact, some TLR agonists and TLR modulators have been investigated as potential drugs on clinical trials and research programmes (Hennessy et al., [@B6]; Murgueitio et al., [@B12]). Plant lectins and toll-like receptors ===================================== Lectins have been extensively used as valuable tools in the biomedical research. The versatility of these biomolecules is due to their interactions with receptor-linked glycans on cell surfaces, which may trigger cell signaling and physiological responses (Lam and Ng, [@B7a]). Plant lectins are characterized as immunomodulator agent, which result in the production of certain cytokines and reactive species and induce efficient immune responses against tumors or microbial infections. A very comprehensive review of immunomodulatory lectins has recently been published by Souza et al. ([@B17a]). In order to investigate the mechanism of this action, some researchers correlated the activation of immune cells by lectins with the expression of TLR receptors. Sodhi et al. ([@B17]) investigated the expression of different TLRs induced by the famous lectin from Concanavalin A (Con A) using mouse macrophages as a model. Con A enhanced in vitro expression of TLRs (2--9) and its action was related with JNK, p38, p42/44, and NF-κ B. The authors also showed the heterodimerization of TLR-2 and TLR-6. Additionally, Con A pre-treated-macrophages were more susceptible to induction of proinflammatory cytokines and nitric oxide by different TLR ligands (ZymosanA, PolyI:C, LPS, CpG DNA). In other study, the Korean mistletoe lectin (KML-C) from Viscum album coloratum was shown to be a potent activator of TLR-4. The treatment of mouse peritoneal macrophages with KML-C-induced the upregulation of interleukin-1 receptor-associated kinase-1 (IRAK1) resulting in macrophage activation and TNF-α production, which was not observed when TLR-4 was blocked using a TLR-4-specific neutralizing antibody or TLR-4-deficient macrophages. The expression of TLR-4 was also induced by lectin-like protein from Anoectochilus formosanus (IPAF), resulting in the stimulation of TNF-α and IL-1β, CD86, and MHC II and phagocytic activity (Park et al., [@B15]). The capacity to modulate the TLR were explored to combat the experimental infection of Paracoccidiodes brasiliensis using native and recombinant KM^+^, a mannose-binding lectin from Artocarpus integrifolia. BALB/c mice were infected with P. brasiliensis and after 10 days both proteins were separately administered. KM^+^ treatment reduced significantly colony-forming unit and induced higher levels of nitric oxide, INF-α, TNF-α, and IL-12, which was dependent on TLR-2 (Coltri et al., [@B4]). Recently, in a remarkable paper, phytohaemagglutinin (PHA from Phaseolus vulgaris) and its isoforms were showed as a specific human TLR-4 agonist during an initial screening. This result encouraged the authors to examine the effects of this and other lectins on external (-2/6, -4, and -5) and internal (-3, -7, -8, and -9) human TLRs. In this research, SBA (Soybean agglutinin from Glycine max), PNA (peanut agglutinin from Arachis hypogaea), ConA and PHA only stimulated extracellular TLRs (-2/6, -4, or -5): TLR-4 for SBA and PNA; TLR-2/6 for ConA; TLR-2/6, -4 and for PHA-L. In other hand, WGA (wheat germ agglutinin from Triticum vulgaris) was the most promiscuous lectin activating all tested receptors, except TLR-3 and -4. The jacalin (from Artocarpus integrifolia) was inactive. This variety of TLR agonist pharmacology is related to different sugar ligand specificity of each plant lectins, suggesting that the action is encoded by the carbohydrate recognition motifs on different TLRs (Unitt and Hornigold, [@B18]). TLR agonists have been proposed as adjuvants for vaccines against virus (Behzad et al., [@B3]; Hong et al., [@B7]), bacteria (Hancock et al., [@B5]), parasite (Moon et al., [@B11]) and fungi (LeibundGut-Landmann et al., [@B8]). In conclusion, these observations encourage further studies for the characterization of plant lectins as novel agonists and modulators of TLR receptors. These proteins act by increasing the immune response of the host against microbial infections, thus overcoming their immunosuppressive mechanisms and offers an alternative to combat the increasing drug resistance. These approaches may also provide new insights on TLR biology and aid in the discovery of new targets glycosides useful in therapy. Conflict of interest statement ------------------------------ The Editor and Authors declare that while the authors and reviewer (Rafael E Silva) are affiliated with the same institution there has been no conflict of interest during the review and handling of this manuscript. The authors express their gratitude to the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), to the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), and to the Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco (FACEPE) for research Grants. [^1]: This article was submitted to Antimicrobials, Resistance and Chemotherapy, a section of the journal Frontiers in Microbiology. [^2]: Edited by: James Stach, University of Newcastle, UK [^3]: Reviewed by: Paul D. Brown, University of the West Indies, Jamaica; Rafael De Freitas E. 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Prékopa–Leindler inequality In mathematics, the Prékopa–Leindler inequality is an integral inequality closely related to the reverse Young's inequality, the Brunn–Minkowski inequality and a number of other important and classical inequalities in analysis. The result is named after the Hungarian mathematicians András Prékopa and László Leindler. Statement of the inequality Let 0 < λ < 1 and let f, g, h : Rn → [0, +∞) be non-negative real-valued measurable functions defined on n-dimensional Euclidean space Rn. Suppose that these functions satisfy for all x and y in Rn. Then Essential form of the inequality Recall that the essential supremum of a measurable function f : Rn → R is defined by This notation allows the following essential form of the Prékopa–Leindler inequality: let 0 < λ < 1 and let f, g ∈ L1(Rn; [0, +∞)) be non-negative absolutely integrable functions. Let Then s is measurable and The essential supremum form was given in. Its use can change the left side of the inequality. For example, a function g that takes the value 1 at exactly one point will not usually yield a zero left side in the "non-essential sup" form but it will always yield a zero left side in the "essential sup" form. Relationship to the Brunn–Minkowski inequality It can be shown that the usual Prékopa–Leindler inequality implies the Brunn–Minkowski inequality in the following form: if 0 < λ < 1 and A and B are bounded, measurable subsets of Rn such that the Minkowski sum (1 − λ)A + λB is also measurable, then where μ denotes n-dimensional Lebesgue measure. Hence, the Prékopa–Leindler inequality can also be used to prove the Brunn–Minkowski inequality in its more familiar form: if 0 < λ < 1 and A and B are non-empty, bounded, measurable subsets of Rn such that (1 − λ)A + λB is also measurable, then Applications in probability and statistics The Prékopa–Leindler inequality is useful in the theory of log-concave distributions, as it can be used to show that log-concavity is preserved by marginalization and independent summation of log-concave distributed random variables. Suppose that H(x,y) is a log-concave distribution for (x,y) ∈ Rm × Rn, so that by definition we have and let M(y) denote the marginal distribution obtained by integrating over x: Let y1, y2 ∈ Rn and 0 < λ < 1 be given. Then equation () satisfies condition () with h(x) = H(x,(1 − λ)y1 + λy2), f(x) = H(x,y1) and g(x) = H(x,y2), so the Prékopa–Leindler inequality applies. It can be written in terms of M as which is the definition of log-concavity for M. To see how this implies the preservation of log-convexity by independent sums, suppose that X and Y are independent random variables with log-concave distribution. Since the product of two log-concave functions is log-concave, the joint distribution of (X,Y) is also log-concave. Log-concavity is preserved by affine changes of coordinates, so the distribution of (X + Y, X − Y) is log-concave as well. Since the distribution of X+Y is a marginal over the joint distribution of (X + Y, X − Y), we conclude that X + Y has a log-concave distribution. Notes References Category:Geometric inequalities Category:Integral geometry Category:Real analysis Category:Theorems in analysis	3.140625	3	[ -0.01031494140625, -0.0032806396484375, 0.020751953125, -0.0034027099609375, -0.005218505859375, -0.012939453125, -0.00921630859375, -0.001739501953125, -0.01165771484375, -0.003082275390625, -0.00634765625, 0.00762939453125, -0.04833984375, -0.00921630859375, 0.005126953125, -0.01092529296875, -0.016845703125, 0.00125885009765625, 0.03466796875, -0.01068115234375, -0.049072265625, 0.01055908203125, -0.004150390625, 0.0159912109375, -0.00567626953125, -0.01043701171875, 0.0052490234375, -0.01336669921875, -0.00958251953125, 0.00494384765625, 0.00018787384033203125, -0.00109100341796875, -0.0084228515625, 0.02294921875, 0.00543212890625, -0.007080078125, 0.01507568359375, 0.0038299560546875, 0.012939453125, -0.015869140625, -0.00421142578125, -0.0130615234375, 0.0002460479736328125, 0.021728515625, 0.0036773681640625, -0.0198974609375, -0.03125, 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Data circuit-terminating equipment A data circuit-terminating equipment (DCE) is a device that sits between the data terminal equipment (DTE) and a data transmission circuit. It is also called data communication(s) equipment and data carrier equipment. Usually, the DTE device is the terminal (or computer), and the DCE is a modem. In a data station, the DCE performs functions such as signal conversion, coding, and line clocking and may be a part of the DTE or intermediate equipment. Interfacing equipment may be required to couple the data terminal equipment (DTE) into a transmission circuit or channel and from a transmission circuit or channel into the DTE. Usage Although the terms are most commonly used with RS-232, several data communication standards define different types of interfaces between a DCE and a DTE. The DCE is a device that communicates with a DTE device in these standards. Standards that use this nomenclature include: Federal Standard 1037C, MIL-STD-188 RS-232 Certain ITU-T standards in the V series (notably V.24 and V.35) Certain ITU-T standards in the X series (notably X.21 and X.25) A general rule is that DCE devices provide the clock signal (internal clocking) and the DTE device synchronizes on the provided clock (external clocking). D-sub connectors follow another rule for pin assignment. DTE devices usually transmit on pin connector number 2 and receive on pin connector number 3. DCE devices are just the opposite: pin connector number 2 receives and pin connector number 3 transmits the signals. When two devices, that are both DTE or both DCE, must be connected together without a modem or a similar media translator between them, a crossover cable must be used, e.g. a null modem for RS-232 or an Ethernet crossover cable. See also Networking hardware References External links Data Terminating Equipment or Data Circuit-Terminating Equipment speeds, IBM Category:Data transmission Category:Telecommunications equipment	3.078125	3	[ -0.009033203125, -0.0004062652587890625, 0.00543212890625, 0.00067138671875, 0.00830078125, -0.01318359375, -0.0191650390625, -0.006500244140625, -0.00836181640625, 0.02197265625, 0.00421142578125, 0.0128173828125, -0.03369140625, 0.002685546875, -0.00897216796875, -0.01300048828125, -0.00689697265625, -0.018798828125, 0.029296875, -0.00921630859375, -0.055419921875, -0.01068115234375, 0.0079345703125, 0.00787353515625, 0.0024871826171875, -0.0235595703125, 0.0213623046875, -0.009765625, -0.004547119140625, 0.00933837890625, 0.0031280517578125, -0.0162353515625, 0.000446319580078125, 0.0281982421875, 0.0089111328125, -0.0111083984375, 0.006256103515625, 0.004241943359375, 0.039794921875, -0.036376953125, -0.006866455078125, -0.0166015625, 0.0120849609375, 0.0303955078125, 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Various techniques of etching resist-imaged photomasks, silicon wafers or other semiconductor materials have been used in semiconductor fabrication processes. A wet etching technique conducted in an immersion tank is a practical high-throughput, flexible fabrication process. By properly selecting etchant chemicals, etch reactions with the target film are thermodynamically favored over reactions with other films. Desirable etch-rate ratios can usually be obtained. A wet etching method is especially suitable for the blanket etching of polysilicon, oxide, nitride and metal. The method is capable of providing the necessary etch selectivity, a damage-free interface and particle-contamination-free wafers. In more recently developed wet etching technology, automated robotic handling systems and ultra-pure chemicals have been used to further improve particle control and process consistency. A well-controlled wet etching technique is therefore the choice of etching process in VLSI and ULSI fabrication processes. One of the key criteria in carrying out a wet etching process is that the etch products must be soluble in the etchant solution and therefore, no contaminating particles are generated. In an immersion etching process, the volume of the etching tank should be large enough to create enough pressure on the wafer surface in order to dislodge hydrogen gas bubbles evolved during etching reactions; to ensure an accurate balance of the etchant components; to keep the concentration of the etchant relatively constant; and to reduce the number of times the etchant tank must be changed in a production environment. An etchant bath change creates expensive down time, and furthermore, the handling of highly hazardous corrosive materials should be rinimized from a safety standpoint. Wet etching is a frequently used technique for stripping photoresist films from silicon wafers where a complete removal of the resist images without adversely affecting the wafer surface is desired. The resist layer or images should be completely removed without leaving any residues, including contaminant particles that may have been present in the resist. The underlying surface of the photoresist layer should not be adversely affected, for instance, undesirable etching of the metal or oxide surface should be avoided. Liquid etchant strippers should produce reasonable bath yield in order to prevent redeposition of dissolved resist on the wafers. The etchant should completely dissolve the photoresist layer in a chemical reaction, and not just lifting or peeling so as to prevent redeposition. It is also desirable that the etching or stripping time should be reasonably short in order to permit a high wafer throughput. Sulfuric acid (H.sub.2 SO.sub.4) and mixtures of H.sub.2 SO.sub.4 with other oxidizing agents such as hydrogen peroxide (H.sub.2 O.sub.2) are widely used in stripping photoresist or in cleaning a wafer surface after the photoresist has been stripped by other means. For instance, a frequently used mixture is seven parts H.sub.2 SO.sub.4 to three parts of 30% H.sub.2 O.sub.2, or a mixture of 88% sulfuric acid and 12% nitric acid. Wafers to be stripped can be immersed in the mixtures at a temperature between about 100.degree. C. and about 150.degree. C. for 5.about.10 minutes and then subjected to a thorough rinse by deionized water and dried by dry nitrogen. Inorganic chemical resist strippers, such as the sulfuric acid mixtures, are very effective in the residual-free removal of highly postbaked resist. They are more effective than organic strippers and the longer the immersion time, the cleaner and more residue-free wafer surface can be obtained. A typical wet chemical treatment system 10 is shown in FIG. 1. The system has a wet chemical holding tank 12 comprises an inner tank 14 and an outer tank 16. As shown in FIG. 1, the inner tank 14 is usually positioned inside the outer tank 16 and that the sidewall 18 of the inner tank is lower than the sidewall 20 of the outer tank. This allows an operating mode where the inner tank is usually filled first with an etchant chemical through inlets 24 and 26. Inlet 26 to the inner tank 14 also serves as a drain and is connected to drain control valve 28 such that liquid can be drained through outlet 32. Similarly, outlet 34 is connected to the bottom of the outer tank 16 to drain the liquid etchant contained in the outer tank through a drain control valve 36 and the outlet 32. The wet chemical treatment system 10 also includes a recirculating means 40 which has an inlet 42 for receiving a fluid from outlet 34 of the outer tank 16 through passageway 46, and an outlet 44 for feeding to filter means 50. A frequently used recirculating means suitable for the wet chemical treatment system is a mechanical pump that is specially outfitted for transporting corrosive fluids. In such a pump, any components that are in contact with the fluid being pumped is constructed of stainless steel, a corrosion-resistant polymeric material such as Teflon, or a metal coated with a corrosive-resistant polymeric material. The passage tubing 46, the drain control valves 28, 36, and the outlets 26, 34 are similarly constructed of corrosion-resistant materials. The wet chemical treatment system 10 further includes a filter means 50 and a heater means 60. The liquid being pumped by the recirculating means 40 through outlet 44 and passage tubing 52 into inlets 54 and 56 of the filter means 50. The filter means 50 is capable of filtering out particulate contaminants in the wet chemical, especially those of metal particles, such that any contamination of the wafer situated in process tank 14 can be avoided. The filtered wet chemical exits the filter means at outlets 48 and 58 to enter into the heater means 60. In most wet chemical treatment processes, either for cleaning or for etching, the wet chemical can be more efficient in its cleaning or etching function when the temperature of the chemical is raised to above ambient temperature. For instance, for most etching and cleaning processes, a temperature of between about 100.degree. C. and about 150.degree. C. is found to be most suitable. The wet chemical enters the heater through inlet 62 and exits at outlet 66 to return the wet chemical to the inner tank 14 through inlets 24 and 26. The inner tank 14 can be filled with fresh chemicals when needed through a filling means 72 controlled by a fill control valve 74. In the operation of a wet chemical treatment system such as that shown in FIG. 1, the system is normally mounted on a raised floor (or a removable floor) in a semiconductor fabrication facility. A typical mounting method for a wet chemical treatment system is shown in FIGS. 2A and 2B. After the treatment system 10 is positioned on a raised floor 30 with a bottom bracket 38 contacting the floor, the treatment system 10 is fastened to the raised floor 30 by a welded angle 64. The welded angle 64, frequently made of a corrosion-resistant metal, such as stainless steel, is attached to the side frame 68 of the treatment system 10 by bolts 70. Collars 76 are used to secure bolts 70 in their mounting position. The welded angle 64 is further attached to the raised floor 30 by bolts 78 through a horizontal flange 80 of the angle. The thickness of the welded angle or of any other anchoring metal plate should be at least 1 cm. The raised floor is normally fabricated of a grating of aluminum which has a smooth top surface and a corrugated back (not shown). The raised floor 30 may also be fabricated of any other suitable material that has the necessary rigidity and lightweight characteristics for easier removal and installation. The raised floor 30 is positioned on top of an I-beam 82 which is in turn positioned on top of a second I-beam 84. Normally, there is no fastening provided between the raised floor 30 and the top surface 86 of the I-beam 82. The I-beam 82 may be fastened to the second I-beam 84 by any suitable mechanical means such as by bolts, or by welding. The bottom flange 88 of the second I-beam 84 may be fastened to a concrete slab floor 90 by bolts 92. A side view of the welded angle 64 for the wet chemical treatment system 10 is shown in FIG. 2B. In the mounting method shown in FIGS. 2A and 2B, the wet chemical treatment system 10 is only secured to the raised floor 30 that is essentially supported by I-beams that are mounted to a slab floor. The conventional mounting method therefore does not meet the seismic prevention standard that is normally required in fabrication facilities which may be subjected to earthquake damages. The problem can be more serious when the wet chemical treatment system is mounted on a higher floor in a fabrication facility where the effect of an earthquake is more severe. For instance, one of such seismic prevention regulations requires that all equipment foot/frame anchoring mechanism and accessories must be designed to survive a force of 0.35 g.times.2.36, i.e., a force magnified for a 4.sup.th floor installation. It is therefore an object of the present invention to provide a method for mounting a process machine on a removable floor that does not have the drawbacks or shortcomings of the conventional mounting methods. It is another object of the present invention to provide a method for mounting a process machine on a removable floor that meets seismic prevention regulation for the containment of corrosive chemicals in a wet chemical treatment system. It is a further object of the present invention to provide a method for mounting a process machine on a removable floor in a semiconductor fabrication facility such that the process machine can survive earthquakes having a force of 0.35 g.times.2.36. It is another further object of the present invention to provide a method for mounting a semiconductor process machine on a removable floor in a fabrication facility by providing an I-beam equipped with an extended upper flange for supporting the removable floor. It is still another object of the present invention to provide a method for mounting a semiconductor process machine on a removable floor in a fabrication facility by providing an I-beam that is equipped with an extended upper flange for supporting the removable floor and for fastening by mechanical means to the process machine through the removable floor. It is yet another object of the present invention to provide a method for mounting a semiconductor process machine on a removable floor in a fabrication facility by utilizing a modified I-beam for supporting the removable floor and for mounting directly to the process machine. It is still another further object of the present invention to provide an earthquake-proof mounting fixture for mounting a process machine on a removable floor by utilizing an I-beam modified with an extended upper flange for supporting the removable floor and for attaching directly to the process machine through the floor. It is yet another further object of the present invention to provide an earthquake-proof mounting fixture for mounting a process machine on a removable floor by providing an I-beam modified with an extended upper flange for attaching to an L-shaped bracket mounted on the process machine through apertures provided in the removable floor.	3.21875	3	[ -0.00848388671875, 0.0166015625, 0.01214599609375, 0.0021514892578125, -0.004486083984375, 0.0107421875, 0.006561279296875, 0.00457763671875, -0.010986328125, -0.0159912109375, -0.00927734375, 0.00836181640625, 0.007171630859375, 0.006591796875, 0.009765625, 0.010498046875, 0.01123046875, -0.0169677734375, 0.017333984375, -0.0224609375, 0.0023956298828125, -0.007049560546875, 0.004638671875, 0.0023651123046875, 0.00213623046875, -0.00732421875, 0.0021209716796875, -0.005584716796875, -0.005523681640625, 0.005035400390625, 0.01239013671875, -0.000598907470703125, 0.02734375, 0.016845703125, -0.004364013671875, 0.005615234375, 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Introduction {#sec1} ============ When individuals prioritize themselves over their communities, the consequences can damage global economies, scientific institutions and the planet. Philosophers and scientists have debated the origins of human prosociality for centuries ([@ref13]). The study of cooperation has evolved beyond philosophy and consumed the energy of scientists across numerous disciplines, from primatology to economics ([@ref7]; [@ref14]). To better understand the nature of cooperation, we took an interdisciplinary approach that combined neuroeconomics, social and personality psychology, and cognitive neuroscience. We examined the neural systems that guide cooperation in groups, and how these systems are shaped by social norms and individual differences. For many years, prosocial restraint models asserted that cooperation stems from deliberate restraint of selfish impulses ([@ref58]; [@ref15]; [@ref31]). More recently, prosocial intuition models have argued that cooperation stems from intuition, whereas deliberation always maximizes self-interest ([@ref50]; [@ref48]). Both models carve the mind into two core processes: intuition (i.e. rapid, automatic, reflexive mental processing) and deliberation (i.e. delayed, controlled, reflective processing). They differ on the role these processes play in promoting selfish vs collective interest. Despite extensive research on this issue, studies of the mental processes underlying cooperation have yielded mixed evidence for existing theoretical models ([@ref6]; [@ref49]). To help reconcile these issues, we considered an alternative approach to cooperation. Value-based decision models argue that the cooperative decisions hinge on preferences that vary between individuals and situations. According to this approach, the neural systems involved in storing, representing and learning value play a role in all decisions, whether they are motor actions, food preferences or cooperative behavior ([@ref9]; [@ref38]; [@ref33]). By specifying the conditions under which cooperation requires effortful deliberation, value-based models explain when (and for whom) interventions to boost cooperation will be most effective. Furthermore, these models can reconcile opposing predictions from prosocial restraint and prosocial intuition models. For instance, consider two car drivers (one prosocial and the other selfish) who witness a collision and decide to pull over and help. Although the driver with prosocial preferences might find the decision to pull over easy, the selfish driver might find the decision hard. Understanding the value each individual places on human welfare may determine which processes produce cooperation. Research on human cooperation often involves social dilemmas, such as the public goods game (PGG). In this economic game, players can make monetary contributions to their group that get multiplied and distributed equally (including to players who keep all their money for themselves). It is in the group's collective interest if all players contribute, but it is in each individual's self-interest to contribute nothing and reap the benefits of other's generosity (i.e. free-riding). Consistent with the prosocial intuition model, faster decisions have been associated with larger group contributions in a PGG, suggesting intuitive cooperation ([@ref50]). However, value-based models posit that longer decisions reflect decision-conflict during choices in which the agent is close to being indifferent between options ([@ref16]). In addition, prosocial individuals (i.e. those who generally help others) are faster to cooperate than free-ride (i.e. prioritize themselves over the group), whereas selfish individuals are faster to free-ride than cooperate ([@ref29]; [@ref32]). Thus, individual differences in prosociality shape which mental computations steer cooperation ([@ref63], [@ref64]). The value-based approach also contends that situational factors shift these mental computations. Increasing the cost of cooperation renders selfish decisions faster and less conflicted ([@ref32]). Therefore, descriptive norms (i.e. perceptions of typical social behavior) may also shape cooperation. Humans have strong needs for belonging and tendencies toward conformity ([@ref1]; [@ref10]; [@ref3]), and norms can increase prosocial behavior ([@ref45]) as well as the intrinsic value of socially preferred stimuli ([@ref66]). Indeed, one's cooperation is related to the mean levels of cooperation of others around ([@ref57]). As a result, it may take more effort to defy group norms---cooperating when others are selfish or free-riding when others are generous. In sum, whether people are faster to cooperate or free-ride depends on their prosocial tendencies and context. We examined whether neural regions involved in decision-making show a similar pattern. While early evidence from neuroimaging studies implicated the ventromedial prefrontal cortex (vmPFC) in affective evaluations ([@ref4]; [@ref56]; [@ref35]), the vmPFC is now widely considered a hub for value-based decision-making. For instance, activity in vmPFC is proportional to the expected value that would be obtained by taking an action ([@ref30]; [@ref38]). In contrast, the dorsolateral prefrontal cortex (dlPFC) is associated with executive function and supports goal pursuit ([@ref8]). Indeed, dlPFC damage impairs executive functions like working memory, reasoning and self-regulation ([@ref67]). Functional connectivity between dlPFC and vmPFC is thought to reflect modulation of value during goal-directed decisions ([@ref26]). Moreover, the connectivity of these regions hinges on individual preferences (e.g. healthy eating among dieters; [@ref26]) and context (e.g. regulating cravings; [@ref28]). In sum, vmPFC activation reflects expected value whereas dlPFC may index overcoming prepotent response tendencies ([@ref2]), decision difficulty ([@ref55]) and goal-directed modulation of vmPFC's expected value signal ([@ref52]). This suggests that individuals' prosociality and the social contexts in which they are embedded should determine the value of cooperation. According to the value-based approach, we should observe greater vmPFC activity during choices that align with one's prosocial tendency since value computations will be higher. Likewise, we should observe dlPFC-vmPFC connectivity during choices that conflict with this tendency, since the dlPFC will need to modulate value signals in the vmPFC to steer decision-making. In this manner, fMRI can provide insight into group-based cooperation. Indeed, past research has found roles for vmPFC and dlPFC in cooperation consistent with a value-based approach ([@ref47]). For instance, people show greater activation in vmPFC when mutually cooperating in a Prisoner's Dilemma ([@ref53], [@ref54]) or when inferring cooperative intentions in others ([@ref11]). However, people show enhanced dlPFC activity when cooperating in a Prisoner's Dilemma with someone who typically defects ([@ref59]) or when trusting out-group members in a Trust Game ([@ref27])---situations that might require modulating prepotent value representations. Moreover, a recent study found that patients with dlPFC damage were less likely to cooperate in a Public Goods Game ([@ref65]), again highlighting that dlPFC can contribute to cooperative choice. To clarify the contributions of these regions in group-based cooperation, we examined here how individual differences and social norms shape vmPFC and dlPFC activity during contributions to public goods. Current research {#sec2} ---------------- We examined two variables that could influence the neural computations underlying cooperation: (1) prosocial tendencies and (2) descriptive norms. We measured brain activity while participants played one-shot PGGs ostensibly with other university students. Prosocial tendencies were measured as the proportion of cooperative PGG decisions made by each participant ([@ref32]). To test that PGG decisions reflected broader individual differences in prosociality, we further measured giving in a dictator game (see Supplemental Section S7). We created prosocial and antisocial social norms by manipulating the feedback from the other university students in the PGG (see [Figure 1](#f1){ref-type="fig"}). To verify these norms, we asked participants to estimate how often students cooperated at each university. These estimates indexed individual differences in norm detection. ![Public goods game with descriptive norm manipulation. (a) At the beginning of each block, participants were instructed, 'You will now encounter students from University \[X/Y\]' with one of the corresponding emblems shown. The base rates were fixed for each university such that 30% of students cooperated in one university (antisocial) whereas 70% of students cooperated in the other (prosocial). Participants alternated between antisocial and prosocial schools (order counterbalanced) for a total of four blocks with 25 trials within each block. (b) Each trial consisted of a decision phase (4 s) and a feedback phase (7 s) that was broken down into three stages: (1) each student's contribution to the public pot, (2) the pot multiplying by two and (3) each student's earnings after the pot is evenly divided four ways. Students who gave to the pot were always pictured in blue whereas students who kept their money were displayed in yellow. ITI and ISI durations were jittered in order to dissociate neural activity between decision and outcome phases.](nsaa055f1){#f1} We tested four hypotheses derived from the value-based approach: (VB~H1~) prosocial tendencies will moderate the relative contribution of vmPFC and dlPFC, such that choices aligned with one's tendency (i.e. selfish participants free-riding or prosocial participants cooperating) will elicit greater vmPFC responses whereas (VB~H2~) choices that conflict with one's tendency (e.g. selfish participants cooperating or prosocial participants free-riding) will elicit greater dlPFC-vmPFC connectivity. Social context should moderate activity in these regions, such that (VB~H3~) deviating from group norms (i.e. cooperating with free-riders or free-riding against cooperators) will elicit greater dlPFC-vmPFC connectivity whereas (VB~H4~) complying with group norms (e.g. cooperating with cooperators or free-riding against other free-riders) will elicit greater vmPFC activity. Methods {#sec3} ======= Participants {#sec4} ------------ Our target sample was 45--50 participants. Forty-seven university students (32 female) were recruited (via online posters) from the New York City area and paid \$20 (or two research credit hours). Students (M = 20.85, SD = 2.60) spanned across 16 north-eastern colleges. All participants were right-handed, healthy, had normal or corrected-to-normal vision, and had no history of psychiatric diagnoses, neurological or metabolic illnesses. The study was approved by the review board of New York University. We report how we determined sample size, all data exclusions, all manipulations and all measures. Five participants were excluded from analyses, leaving a sample of 42 participants. Participants were excluded if they met at least one of the criteria defined prior to data collection: (1) moving at least 3 mm across all scan sessions and (2) reporting suspicion (during debriefing) that their decisions could actually affect the payment of other participants. One participant was excluded due to criterion 1 (\>5 mm motion in each scan session), and four participants were excluded due to criterion 2. Procedure {#sec5} ========= Public goods game {#sec6} ----------------- Participants received instructions on how to play a PGG, including four practice trials and a thorough comprehension quiz. In each round, participants were given \$8.00, which they could either keep for themselves or contribute to benefit the group. Players interacted in groups of four and contributions were doubled and split equally by all group members. On each trial, participants were given 4 s to make a decision and received no payment on trials where no response was recorded. After each choice, participants were shown feedback about the other players' decisions and resulting payouts. An intertrial interval (ITI) signaled the beginning of each round and a fixation cross interstimulus interval (ISI) separated the decision and feedback stages ([Figure 1B](#f1){ref-type="fig"}). ITIs and ISIs were jittered 1--8 s using a Poisson distribution and randomized between participants. Participants were instructed they would never encounter the same player more than once such that each trial resembled a one-shot PGG. Before beginning the game, we informed participants that the other players' decisions were based on previous responses from students attending two universities whose identities we had concealed (labeled University X and University Y; [Figure 1A](#f1){ref-type="fig"}). Participants were further instructed that students from one university were more likely to give their money (prosocial school) whereas students from the other university were more likely to keep their money (antisocial school). We did not specify which university was prosocial and antisocial. Participants alternated between playing with students from the prosocial and antisocial schools across four blocks for a total of 100 trials. The identity of the universities and the order they were encountered were counterbalanced across participants. In reality, we adjusted the base rates such that players from each university gave 70% (prosocial) or 30% (antisocial) of the time. Of the 50 trials playing with the prosocial university, for instance, participants encountered 105 'givers' (out of 150 students) with the following feedback distribution: 0 givers (2 trials), 1 giver (10 trials), 2 givers (20 trials) and 3 givers (18 trials). Earnings across all trials were averaged and paid to participants after the study. Prosocial tendencies were computed for each participant by computing their mean level of cooperation (i.e. the proportion of trials they decided to give). Two survey measures were collected and analyzed for exploratory analyses reported in the supplement: emotional ratings for each PGG outcome (see Supplementary Sec. S1) and group identification with each university ([@ref60]) (see Supplementary Sec. S2). Additional survey measures were collected at the end of the study but are not included in the present analyses[^1^](#fn1){ref-type="fn"}. Dictator game {#sec7} ------------- As an independent measure of prosociality, participants played two dictator games upon exiting the scanner: one with a student from the prosocial school and one with a student from the antisocial school. Participants could allocate anywhere from \$0.00---\$1.00 to each student using a slider bar. The amount given to both groups was averaged into an overall measure of prosociality. At the end of the study, participants were informed that no students were actually going to be paid and they were paid the full \$2.00 they were originally endowed with (regardless of their actual allotment). Explicit estimation {#sec8} ------------------- We next assessed the extent to which students' explicitly learned the social norms. Using a slider bar, participants estimated the percentage of students that cooperated from each school. We took the difference between these scores for each participant to compute a measure of norm detection (i.e. the extent to which students from the prosocial school cooperated more often than the antisocial school). Positive scores indicate students who (correctly) remembered the prosocial school giving more often whereas negative scores indicate students who (incorrectly) remembered the antisocial school giving more often. Behavioral analyses {#sec9} ------------------- Analyses of cooperative behavior were conducted using generalized estimating equations ([@ref39]) (GEE) with an exchangeable correlation structure clustered on each participant[^2^](#fn2){ref-type="fn"}. These procedures account for repeated measures in a regression framework and were implemented using the geepack package ([@ref25]) in R ([@ref12]). We used logistic regression with cooperation operationalized as a binary outcome for each trial (0 = Keep, 1 = Give). Parametric tests were only conducted on measures where we observed insufficient evidence for non-normality (α = 0.05; Shapiro--Wilk test). Otherwise, bootstrap confidence intervals were computed with 10 000 simulations. fMRI data acquisition {#sec10} --------------------- Functional imaging was conducted using a Siemens (Erlangen, Germany) 3.0 Tesla Allegra head-only MRI scanner. Functional images were acquired using a customized multi-echo EPI sequence developed by the NYU Center for Brain Imaging to mitigate the effects of susceptibility artifacts in medial temporal and ventromedial regions (TR = 2000 ms; TE = 15 ms; Flip Angle = 82°; 34 3 mm slices with a 0.45 mm gap for whole-brain coverage, Matrix = 64 × 80; FOV = 192 × 240 mm; Acquisition voxel size = 3 × 3 × 3.45 mm). This sequence has been described in detail in prior work ([@ref24]). Each volume comprised 34 axial slices collected in an interleaved-ascending manner and parallel to the AC-PC line. Data were collected in four sessions, 225 volumes each (7 min and 30 sec). Six scans were acquired at the start of each run and dropped from analysis to allow magnet equilibration. During this time, participants were told which university they would be playing with. Finally, whole-brain high-resolution structural scans (T1-weighted, MPRAGE, 1 × 1 × 1 mm resolution) were acquired from all participants, coregistered with their mean EPI images and averaged together to permit anatomical localization of the functional activations at the group level. fMRI data pre-processing {#sec11} ------------------------ Image analysis was performed using SPM12. Images were corrected for slice-time acquisition and realigned to correct for participant motion, coregistered to structural images, transformed to conform to the default T1 Montreal Neurological Institute (MNI) brain interpolated to 3 × 3 × 3 mm, smoothed using a Gaussian kernel with a full-width-at-half-maximum of 6-mm, corrected for artifacts using the ArtRepair toolbox ([@ref41]) and detrended using the LMGS toolbox ([@ref40]). The blood-oxygenation-level-dependent (BOLD) signal was modeled using a canonical hemodynamic response function. A general linear model (GLM) included (1) onset of give decisions, (2) onset of keep decisions, (3) onset of feedback after give decisions and (4) onset of feedback after keep decisions. Reaction times were entered for decision epoch durations, such that each trial was modeled as having a duration of the participant's reaction time ([@ref23]). Further regressors of no interest included (5) onsets of choice epochs for missed trials (i.e. non-responses), (6) feedback epochs for missed trials, as well as six movement parameters from the realignment stage. A high-pass filter with cutoff period of 128 s was used. To analyze the impact of prosocial tendencies, first-level contrasts for Give \> Keep were generated and entered into a second-level random effects analysis along with each participant's mean cooperation (i.e. proportion of give decisions) as an interaction term. To analyze the impact of descriptive norms, first-level contrasts for Give \> Keep were generated separately for each of the four scanner sessions. Norm-level contrasts were computed for each participant by averaging session contrasts corresponding to each norm and then subtracting the antisocial contrast from the prosocial contrast. These contrasts were then entered into second-level random effects analyses. For a psychophysiological interaction (PPI) analysis of overall choice, vmPFC activity served as a physiological variable, choice type (free-riding vs giving) served as a psychological variable, and the interaction of these variables was examined; individual differences in prosociality served as a moderator in a second-level analysis. For a PPI analysis of norm congruence, vmPFC activity served as a physiological variable, choice type (congruent with norm vs deviant from norm) served as a psychological variable, and the interaction of these variables was examined; individual differences in norm detection served as a moderator in a second-level analysis. Based on past work, our hypotheses targeted specific regions of interest (ROIs): the vmPFC and the dlPFC. To constrain our analysis to these regions, we used existing ROI masks for vmPFC and dlPFC based on prior work ([@ref65]). These ROIs were constructed with the MarsBar toolbox by combining corresponding structures from the Harvard--Oxford Maximum Probability Atlases ([@ref20]) (see [Supplementary Figure S6](#sup1){ref-type="supplementary-material"}). The vmPFC ROI consisted of the frontal pole, frontal medial cortex, paracingulate gyrus, subcallosal cortex, constrained by rectangular prism X = \[−14, 14\], Y = \[10, 80\], Z = \[−35, 0\]. The dlPFC ROI consisted of the frontal pole, inferior frontal gyrus and middle frontal gyrus, constrained by bilateral rectangular prism X = \[−60, −30 (L); 30, 60 (R)\], Y = \[20, 70\], Z = \[5, 55\]. Small-volume corrections were conducted using these ROI masks. Unless otherwise noted, all analyses were corrected for multiple comparisons using a voxel-wise height threshold of P \< 0.001 combined with an appropriate cluster extent to maintain a family-wise error (FWE) rate of P \< 0.05, using Gaussian random field theory as implemented in SPM ([@ref21]). ROI effect size estimation {#sec12} -------------------------- Given the difficulty of drawing conclusions from null results, we conducted the following procedure to estimate effect sizes for non-significant contrasts. Using Marsbar, we first extracted each subject's average betas (i.e. predicted amplitude) for each contrast within each ROI mask. We then computed the mean amplitude across 10 000 bootstrapped simulations and report the 95% confidence interval of the resulting distribution of means. Computational model {#sec13} ------------------- We fit a computational model that estimated participants' trial-by-trial expectations about the number of expected givers on each round. This model assumed participants chose to give or keep based on (1) a constant term and (2) the number of expected givers on a given round:$$\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}\begin{equation} p{G}_t=\frac{1}{1+{e}^{\left(-c+-\beta \times G\right)}} \end{equation}\end{document}$$where $\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}${pG}_t$\end{document}$ is the probability of giving on trial t, c is a constant term, $\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}$\beta$\end{document}$ is a weight on the expected number of givers for that trial and $\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}$G$\end{document}$ is the expected number of givers. Separate estimates of G were held for each university. On each trial, G was updated for the relevant university using a delta-learning rule:$$\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}\begin{equation} {G}_t={G}_{t-1}+\alpha \delta \end{equation}\end{document}$$where $\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}$ \alpha$\end{document}$ is a learning rate parameter and $\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}$\delta$\end{document}$ is a prediction error related to the expected number of givers:$$\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}\begin{equation} \updelta= Number\ of\ Givers\ - G\end{equation}\end{document}$$ The number of givers was rescaled to range from −1 to 1, so that the constant term would be interpretable at the mean number of givers. Finally, given that the proportion of givers in each group did not change over time, participants could learn the contingencies relatively early on. We therefore allowed the learning rate to decay over time with a decay parameter d between 0 and 1 ([@ref43]):$$\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}\begin{equation} {\alpha}_t={\alpha}_{t-1}\times d \end{equation}\end{document}$$ This model was fit using maximum likelihood estimation. We applied parameters derived from the model to each participant's data to compute trial-by-trial estimates for the expected number of givers for each participant (see Supplementary Sec. S5 for more details on the modeling approach and [Supplementary Table S2](#sup1){ref-type="supplementary-material"} for parameter estimates). This time series was entered as a parametric modulator of choice, using the same first-level fMRI GLM described in the primary analysis. This analysis was whole-brain corrected for multiple comparisons. Data availability {#sec14} ----------------- All relevant and deidentified, pre-processed data and materials have been made publicly available at the following OSF link: (<https://osf.io/hfngs/>). Results {#sec15} ======= Behavioral Results {#sec16} ------------------ Prosocial tendencies. On average, participants cooperated on 33.57% of the trials (SD = 28.40%). Nonetheless, there were large individual differences between participants, ranging from one participant who always cooperated to seven free-riders who chose to keep on all 100 trials (see [Supplementary Figure S1](#sup1){ref-type="supplementary-material"}). Reaction times did not vary between giving and keeping or between norm condition. However, RTs did depend on individual differences in prosocial tendencies, such that cooperation tended to be faster among prosocial participants (see Supplementary Sec. S3). Descriptive norms. To ensure participants encoded the descriptive norm manipulation, we conducted a paired t-test to assess whether participants estimated different rates of cooperation between the schools (i.e. norm detection). Participants noticed that students from the prosocial school cooperated more often (M = 54.71%, SD = 23.37%) than students from the antisocial school (M = 32.10%, SD = 21.30%), suggesting they learned that group norms differed, t(41) = 4.34, d = 0.67, P \< .001 (see [Supplementary Figure S3](#sup1){ref-type="supplementary-material"}). In turn, descriptive norms impacted cooperation. Participants were more likely to cooperate with students from the prosocial school (M = 40.42%, SD = 49.08%) than the antisocial school (M = 24.08%, SD = 42.77%; Odds ratio = 2.15, Wald χ^2^(1) = 26.4, P \< 0.001; see Supplementary Sec. S3 for reaction time analysis). Moreover, norm compliance (i.e. preferential cooperation with the prosocial vs antisocial school) was associated with norm detection (M = 22.62%, SD = 33.77%; r(40) = 0.36, bootstrapped 95% CI: \[0.12, 0.55\]): participants who correctly recalled greater cooperation from the prosocial school were more cooperative towards the prosocial school. Neuroimaging results {#sec17} -------------------- Overall cooperation. We first tested whether cooperation and defection overall were associated with neural activation in vmPFC and dlPFC. Such findings could be consistent with models asserting that intuition drives cooperation and deliberation promotes self-interest (prosocial intuition; [@ref50], [@ref51]) or that humans are impulsively selfish and require self-control to cooperate (prosocial restraint; [@ref58]; [@ref31]). We tested the first prosocial restraint hypothesis by examining whether the mean signal within vmPFC (defined through an anatomical region of interest; see Methods) was higher during free-riding as opposed to cooperation (i.e. Give \> Keep). Therefore, seven participants with invariant decisions (i.e. cooperating or free-riding on every trial) were excluded from this analysis, leaving 35 participants. No significant vmPFC activation was observed in this contrast at thresholds with small volume corrections (p~voxel~ \< 0.001; p~cluster~ \< 0.05). We then examined whether dlPFC activity increased during cooperation vs free-riding (i.e. Keep \> Give), but observed no significant difference. We reversed these contrasts to test the two prosocial intuition hypotheses: vmPFC is more active when cooperating (i.e. Keep \> Give) and dlPFC activity increases during free-riding (i.e. Give \> Keep). However, we did not observe significant differences for these contrasts. Bootstrapped 95% confidence intervals of the signal change for cooperative (relative to selfish) choices indicated that mean vmPFC signal may increase up to 0.387% or decrease up to 0.474% whereas mean dlPFC signal may increase up to 0.224% or decrease up to 0.173%. Thus, we found insufficient evidence that these regions were differentially recruited for cooperation or free-riding. These results were not consistent with simplified prosocial restraint or prosocial intuition models of cooperation. Thus, we examined whether activation in these regions depends on cooperative tendencies and social norms. Prosocial tendencies. According to the value-based approaches, vmPFC should be more responsive during choices aligned with one's prosocial tendencies: selfish participants should display greater vmPFC responses when free-riding and prosocial participants should display greater vmPFC responses when cooperating (see VB~H1~). This is because vmPFC has been found to represent the difference in value between chosen vs unchosen options ([@ref5]; [@ref42]; [@ref24]). As a result, vmPFC activity should be higher for a prosocial participant when giving (i.e. when relative value is higher) than when keeping (i.e. when relative value is lower). For a free-riding participant, the reverse should be true. To test this hypothesis, we entered each participant's mean cooperation into a second-level GLM as an estimate of prosociality, and then tested the interaction between prosociality and decision type (i.e. cooperate vs free-ride)[^3^](#fn3){ref-type="fn"}. We observed a cluster of vmPFC for the interaction of Prosociality x Decision, t(33) = 4.99, k = 53, p~cluster~ \< 0.001 ([Figure 2A and B](#f6){ref-type="fig"}; see [Supplementary Table S1](#sup1){ref-type="supplementary-material"})[^4^](#fn4){ref-type="fn"}. Consistent with value-based approach, decisions that aligned with one's prosociality elicited greater vmPFC activity: free-riders had more vmPFC activity when free-riding, whereas cooperators had greater vmPFC activity when cooperating. ![vmPFC activity and dlPFC-vmPFC connectivity is moderated by prosocial tendencies. Average cooperation moderates (a) BOLD response in vmPFC and (c) right dlPFC activity during Give (vs Keep) decisions. Color indicates magnitude of t statistic. As an alternate visualization, (b) vmPFC cluster betas (y-axis) for each participant (n = 35) are plotted against the proportion of cooperative trials (x-axis). (d) Right dlPFC-vmPFC PPI cluster betas (y-axis) are plotted against the proportion of cooperative trials (x-axis). Robust linear regression fits are displayed with blue lines and surrounding 95% confidence interval band.](nsaa055f2){#f6} We examined whether prosociality moderated dlPFC activity during choices that conflicted with prosociality (i.e. selfish participants cooperating or cooperative participants free-riding). For this prosociality × decision interaction, we observed two clusters within right dlPFC (both with equal cluster sizes, k = 13, p~cluster~ = 0.050). More prosocial participants showed greater right dlPFC activity when free-riding whereas participants with selfish tendencies showed greater activity when cooperating (see [Figure 2C](#f6){ref-type="fig"}). Moreover, we obtained the same findings when using a self-report measure of cooperative preferences that was not derived from behavior and was not specific to either norm context. Specifically, after the main task, participants reported how positively and negatively they felt upon giving and keeping; when using relative positive affect during giving vs keeping as an alternative measure of individual cooperative preference, we observed the same patterns of activation in vmPFC and dlPFC described above (see Supplemental Figure S5, and Supplementary Sec. S1). Some value-based models also assert that dlPFC and vmPFC become temporally correlated when making more difficult, goal-directed choices (see VB~H2~). To test this prediction, we examined whether functional connectivity between dlPFC-vmPFC was moderated by prosociality. We conducted a psychophysiological interaction (PPI) analysis with the right dlPFC cluster for non-dominant choices ([Figure 2C](#f6){ref-type="fig"}) and the vmPFC cluster for dominant choices as a seed region ([Figure 2A](#f6){ref-type="fig"}). We examined connectivity as a function of cooperative vs free-riding decisions, with prosociality serving as an individual difference. Cooperative participants showed greater right dlPFC-vmPFC connectivity when free-riding, whereas selfish participants showed greater connectivity when cooperating, r(33) = −0.23, bootstrapped 95% CI: \[−0.56, −0.04\], t~R~ = −2.00 ([Figure 2D](#f6){ref-type="fig"})[^5^](#fn5){ref-type="fn"}. In other words, participants showed greater dlPFC-vmPFC connectivity when making choices that ran counter to their prosociality, consistent with the value-based approach. Social norms. If norms amplify the value of conformity ([@ref44]), then a value-based approach would predict greater dlPFC-vmPFC connectivity when choosing to deviate from norms (i.e. cooperating in antisocial groups or free-riding in prosocial groups; see VB~H3~). We tested this prediction by conducting another PPI analysis with the dominant choice vmPFC cluster ([Figure 2A](#f6){ref-type="fig"}) as the seed region and the non-dominant choice dlPFC cluster ([Figure 2C](#f6){ref-type="fig"}). We contrasted deviant vs compliant decisions (i.e. cooperating with the prosocial group and free-riding with the antisocial group vs free-riding with the prosocial group and cooperating with the antisocial group)[^6^](#fn6){ref-type="fn"}. We did not observe any significant connectivity changes across decision type: bootstrapped confidence intervals for deviant (vs compliant) choices indicated mean dlPFC connectivity may increase up to 0.172% or decrease up to 0.189%. Our measure of norm detection indicated that not all participants learned the group norms. Since this norm-detection measure was positively associated with behavioral norm compliance, it seemed possible that norms modulated dlPFC-vmPFC connectivity in a manner dependent on how participants perceived the norms. To test this possibility, we conducted an exploratory analysis similar to our individual difference analysis above: we entered individual differences in norm detection as a predictor in the second-level GLM. We observed a positive correlation between norm detection and dlPFC-vmPFC connectivity: participants who correctly perceived the norms elicited greater right dlPFC-vmPFC connectivity when deviating from the group, r(33) = 0.50, bootstrapped 95% CI: \[0.22, 0.69\], t~R~ = 2.90 ([Figure 3](#f16){ref-type="fig"}). This suggests that vmPFC and dlPFC are more functionally correlated when (a) participants who correctly perceived norms deviated from actual group norms and (b) participants who incorrectly perceived norms complied with group norms, thus deviating from their perceived norms. That is, participants who incorrectly perceived norms showed greater vmPFC-dlPFC connectivity when deviating from their subjectively perceived norms, much as participants who correctly perceived norms showed greater vmPFC-dlPFC connectivity when deviating from the objective norms. ![Norm detection moderates dlPFC-vmPFC connectivity when deviating from the norm. Norm detection moderates right dlPFC-vmPFC connectivity for deviant decisions (e.g. free-riding in the prosocial norm or cooperating in the antisocial norm). Participants (n = 34) who perceived relatively more cooperation from the prosocial school vs antisocial school (x-axis) elicited heightened right dlPFC-vmPFC connectivity when deviating from (vs complying with) the group norm (y-axis). To mitigate influential points, a robust linear regression fit is displayed with blue line and surrounding 95% confidence interval band.](nsaa055f3){#f16} We examined whether this connectivity predicted norm compliance (i.e. preferential cooperation with the prosocial vs antisocial school). We observed an interaction whereby participants with greater right dlPFC-vmPFC connectivity during deviant decisions engaged in greater norm-compliant cooperation, OR = 1.97, 95% CI = \[1.26, 3.10\], Wald χ^2^(1) =8.72, P = 0.003. This suggests that vmPFC and dlPFC are more functionally correlated when (a) norm-compliant participants deviate from norms and (b) non-compliant participants comply with norms; the latter finding may reflect the fact that non-compliance was correlated with incorrect perceptions of norms, as reported above. We did not observe a relationship between group norms and vmPFC activity (see Supplementary Sec. S6). Evolving expectations. Adapting to norms requires people to update and deploy expectations about how others will cooperate. We therefore tested whether neural activity during choice reflected expectations about others' cooperation. We fit participant choices to a computational model of learning and choice, which assumed that people updated an estimate of average cooperation for each group following feedback on each trial. Estimates were updated with a prediction error, or the discrepancy between the actual and expected number of cooperators on each trial. This model allowed us to estimate, in a trial-by-trial manner, the number of givers participants expected while making decisions and analyze whether any neural regions tracked this quantity during choice. Increased expectation of givers during choice was associated with activation near the right temporoparietal junction ([Figure 4](#f17){ref-type="fig"}). Given this region's purported role in theory of mind tasks ([@ref22]), this may reflect increased social cognitive processing during choices where others were expected to cooperate. If so, internalizing social norms may play a key role in future cooperation---a form of social prediction. It also suggests participants dynamically tracked expectations related to norms during decision-making. ![rTPJ activity reflects the expected number of givers during decision-making. The number of givers anticipated during choice on a given trial---as estimated through a computational model of learning and choice---correlates with activation in rTPJ. Color indicates magnitude of t statistic.](nsaa055f4){#f17} Discussion {#sec18} ========== Value-based models contend that psychological processes supporting cooperation may hinge on idiosyncratic preferences as well as contextual factors that shift these preferences ([@ref32]; [@ref47]). Consistent with this approach, we find that vmPFC and dlPFC activity during cooperation depends upon individual differences in prosociality and sensitivity to social norms. Specifically, prosocial participants elicited greater vmPFC activity when cooperating as well as heightened right dlPFC activity and dlPFC-vmPFC connectivity when free-riding. Self-serving participants showed the reverse pattern. Thus, neither the vmPFC nor the dlPFC exhibited a consistent role in cooperation, but instead showed greater activation when people acted consistently or inconsistently with their prosocial tendencies, respectively. These findings are consistent with the idea that vmPFC activity reflects a decision value that can be modulated by dlPFC ([@ref52]). In contrast, prominent models rooted in dual-process frameworks argue that cooperation is either reflexive (prosocial intuition models) or primarily stems from deliberate self-control (prosocial restraint models). Past neuroimaging work rooted in dual-process tradition associated vmPFC with intuitive processing and dlPFC with deliberative processing. Thus, the prosocial restraint model implied free-riding would be associated with vmPFC activity and cooperation would be associated with dlPFC activity. In contrast, the prosocial intuition model implied cooperation would be associated with greater vmPFC activity and free-riding would be associated with greater dlPFC activity. When adopting this interpretation of vmPFC and dlPFC, our data still suggest that prosocial participants are intuitive cooperators, which conflicts with prosocial restraint models, and that selfish participants are deliberative cooperators, which conflicts with prosocial intuition models. Thus, our findings support a value-based interpretation of vmPFC and dlPFC activity or require a more flexible dual-process model that can account for the moderating roles of prosociality and norms. The current research further indicates that norms shape cooperation. Participants who were most attentive to norms aligned their behavior with norms and showed greater right dlPFC-vmPFC connectivity when deviating from norms, whereas the least attentive participants showed the reverse pattern. Curiously, we found no clear evidence that decisions to conform were more valued than decisions to deviate. This conflicts with work suggesting social norms boost the value of norm compliance ([@ref44]). Instead, our findings suggest that norm compliance can also stem from increased functional connectivity between vmPFC and dlPFC. Our findings raise questions about how people model the dynamic shifts in norms that vary over time and between groups. We fit a computational model of learning to understand how people represent the cooperation expected from each group. Expectation of givers during decision-making was associated with activation in a region near the right temporoparietal junction---a region related to theory of mind ([@ref22]). This finding comports well with recent work ([@ref46]) and suggests that social cognitive systems may interface with the construction of value to guide decisions. The present research highlights two important factors that modulate the neuro-cognitive processes guiding cooperation: prosociality and social norms. Rather than neural activity in vmPFC always reflecting either prosocial or selfish behavior, the value of cooperation may be lower among selfish individuals or in selfish environments. The notion that cooperation necessarily stems from reflexive intuitions ignores the possibility that some individuals value the outcomes of others. This idea coheres with evidence that selfish participants more often cooperate by mistake, whereas prosocial participants accidentally prioritize their self-interest ([@ref29]). Thus, intuition may trigger cooperative mistakes from selfish participants but deter prosocial participants from second guessing their cooperation. Conclusion {#sec19} ========== In conclusion, more flexible models are needed to specify when, and for whom, cooperation is intuitive or deliberative. This study highlights the advantage of social neuroscience methods for disambiguating the decision-making processes that guide prosocial behavior. The present findings are largely inconsistent with models that assume one mental process always supports cooperation but are consistent with a value-based approach to understanding cooperation. Although our focus on dlPFC and vmPFC helped constrain our hypotheses, cooperation is complex and draws on a widely distributed network of neural systems implicated in prosocial behavior ([@ref34]; [@ref17]; [@ref18]; [@ref29]; [@ref19]). For instance, other reward-related regions, such as caudate, are involved in prosocial choices ([@ref36]) and may show differential patterns of activation across individuals with strong vs weak prosocial preferences. Similarly, as evidence accumulates that moral decisions rely on more dynamic, distributed and multi-faceted neurocognitive processing ([@ref61]), more flexible models of value-based decision-making appear to offer a fruitful account for prosociality. Supplementary Material ====================== ###### Click here for additional data file. We thank E. Owens for assistance with data collection, and members of the New York University Social Perception and Evaluation Laboratory for comments on the manuscript. This work was funded by the New York University Center for Brain Imaging and the US National Science Foundation grant \#1349089 awarded to J.V.B., grant \#1606959 awarded to L.H., and graduate research fellowship awarded to J.W. There are no conflicts of interest to declare. These include the Levenson Self-Report Psychopathy Scale ([@ref37]), Groupiness Scale (Dunham & Van Bavel, unpublished), Social Value Orientation ([@ref62]), and additional demographic information (e.g. political ideology, socioeconomic status, etc.) Unlike traditional OLS regression, GEE parameter estimates are typically evaluated using a Wald χ^2^ distribution with 1 degree of freedom. See Krajbich et al., (2015) for or a similar analytic strategy with behavioral data. The t statistic reported for this contrast (as well as all subsequent contrasts) refers to the peak voxel within the cluster. We use the t~R~ notation to indicate t statistics calculated using the robust linear regression procedure with an M estimator available in the MASS package ([@ref01]) for R ([@ref12]). One additional participant was excluded from this analysis because they never cooperated when playing with the antisocial students. 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Understanding Fusion UNDERSTANDING FUSION Figuring Out Nuclear Fusion.… Contrasted against nuclear fission, the type of nuclear reaction currently in use in our nuclear power plants, nuclear fusion has presented unique challenges that has resisted decades of global efforts and investments into unlocking its secrets. The intense heat and pressure needed to make hydrogen atoms fuse together represents a huge technical problem of nuclear fusion, compared to the simple splitting of heavy atoms (uranium or plutonium) in nuclear fission. Nuclei of lighter atoms collide and fuse together to produce nuclei of heavier atoms and release vast amounts of energy in the process —this is the essence of fusion, and also the energy of this process that powers our Sun. Can we harness this process to meet Earth’s energy demands? Fusion is the process that produces the amazing quantities of energy that pour out of stars, such as our sun. It occurs when light atoms such as hydrogen become so hot that they fuse, into new elements, such as helium, in the process releasing large amounts of energy. The ingredients for this amazing process are abundant on earth, and no greenhouse gases or long-lived nuclear waste are created by fusion. Once harnessed,…Learn more>> euro-fusion.org ccfe.ac.uk- Nuclear fusion is one of the most promising options for generating large amounts of carbon-free energy in the future… To get energy from fusion, gas from a combination of types of hydrogen – deuterium and tritium – is heated to very high temperatures (100 million degrees Celsius). One way to achieve these conditions is a method called ‘magnetic confinement’ – controlling the hot gas (known as a plasma) with strong magnets. The most promising device for this is the ‘tokamak’, a Russian word for a ring-shaped magnetic chamber…Learn more>>ccfe.ac.uk WHY FUSION New, environmentally sustainable forms of electricity will be required to meet the aspirations of a growing world population. By 2050, an expected rise in global population from six billion to nine billion and better living standards could lead to a two to threefold increase in energy consumption. No single technology will fulfil this demand. Each has strengths and weaknesses, and a mix of power sources will be needed to meet the challenges of energy security, sustainable development and environmental protection. Future energy supply options may comprise fossil fuels, nuclear fission, fusion, and renewables. euro-fusion.org- Our current energy landscape is heavily dependent on the fast-depleting fossil fuels, with 80% of the global energy consumption being based on fossil fuels, and changing this dependence is critical for two main reasons. First, to meet the growing energy demand, which is set to increase by 37% by 2040 according to the IEA 2014 Executive Summary, and second, to cut down on the greenhouse gas emissions. Once harnessed, fusion has the potential to be nearly unlimited, safe and CO2-free friendly energy source.euro-fusion.org FUSION PHYSICS…High-school physics teaches us that equally charged particles, instead of colliding, would repel each other. To overcome this repulsion, the nuclei need to collide at high speed, and this is achieved by heating the plasma, which makes all the nuclei whiz around faster. As the plasma gets hotter nuclei start to collide at high speeds, and a small fraction of them stick together, releasing a large amount of energy. euro-fusion.org It seems confusing that energy can be generated by both fusion (the coalescence of two nuclei) and fission (splitting the nucleus), as they appear to be quite opposite processes. The explanation lies in the size of the nuclei… Learn more>>euro-fusion.org FUSION TECHNOLOGYAt the core of the fusion device is a ring-shaped metal vessel. The inner wall of the vessel is lined with removable heat-resistant tiles, and has numerous openings for heating devices and measuring systems. Equally spaced around the device are electromagnets that provide strong magnetic fields to keep the hot plasma away from the reactor walls.…Learn more>>euro-fusion.org JET OPERATIONSLearn more about how tokamaks work by taking a tour through the operation and technology of JET. For anyone looking for even more detail we recommend the book “Focus on” in our download-section.euro-fusion.org JET TECHNOLOGIESJET is a lot more than a doughnut-shaped metal vessel. There is an entire plant comprised of many different systems that work together to create the superheated moments in the torus Myriad systems pump out the air, cool some parts of the experiment, heat others, inject the fuel and control the plasma, and then clean up afterwards, ready to do it all again. euro-fusion.org	3.859375	4	[ -0.01165771484375, -0.021484375, 0.0089111328125, -0.014892578125, -0.0101318359375, 0.0145263671875, -0.019775390625, 0.006927490234375, 0.0052490234375, -0.0262451171875, 0.006256103515625, 0.018798828125, -0.032470703125, -0.002471923828125, 0.002227783203125, 0.0021209716796875, -0.0172119140625, -0.005462646484375, 0.022705078125, 0.0045166015625, -0.03857421875, 0.0247802734375, 0.0181884765625, 0.00799560546875, 0.0010986328125, 0.009033203125, -0.0140380859375, -0.0017547607421875, 0.01239013671875, -0.0108642578125, 0.00099945068359375, 0.005462646484375, -0.014892578125, -0.0031280517578125, 0.00139617919921875, -0.000591278076171875, 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It may be hard to believe in the midst of another contentious election cycle, but the next quarter century in the United States promises to be a period of increasing moderation and stability—at least according to a little-known but compelling theory about how the ratio of available men to available women alters our lives. Ups and Downs of America's Sex Ratio Harvard social psychologist Marcia Guttentag began formulating her theory in 1975, after watching Mozart’s The Magic Flute with her second husband, psychologist Paul Secord, and her two children, Lisa, 16, and Michael, 14. “Nothing is more noble than wife and man, man and wife, and wife and man … [reaching] to the height of Godliness,” sang Papageno and Pamina onstage. Hearing them extoll the virtues of marriage so extravagantly put Guttentag into a kind of “cultural shock,” she later wrote. These were the 1970s, after all, when millions of marriages—including both Guttentag’s and Secord’s first marriages—had collapsed in the chaos of the free love movement spawned during the previous decade. When Guttentag returned home, she and her daughter listened to songs that were popular at the time, all of which had a “love ’em and leave ’em” theme. Why were views on marriage in these two eras—Mozart’s 1790s and America’s 1970s—so very different? Maybe, she conjectured, women were in short supply in Mozart’s day, and perhaps now, in the 1970s, there were just too many women. That became the title of a book Guttentag began writing soon after she had her insight, which she knew was the most important of her career. For the first time in U.S. history, she soon learned, the “availability sex ratio”—the ratio of adult men to adult women who are available to marry—had dropped well below 1.0, to perhaps 0.7 by 1970. This meant that there were now 10 available women for every 7 available men, an excess of millions of women of marrying age. What had caused the sex ratio to drop so dramatically, Guttentag wondered, and what impact did this change have on society? While busy directing two research centers at Harvard University, Guttentag began Too Many Women as a true labor of love. She examined imbalances in the ratio of men to women in various cultures and at various times throughout history and the effects they had on social systems. Among other things, she found that where the sex ratio was high, marriage was stable and women tended to stay home, but where the sex ratio was low (too many women, that is), marriage was unstable and women moved into the workplace. The dramatic differences between Sparta and Athens during the fourth century B.C. drove the point home for Guttentag. Ancient Athens most likely had a sex ratio between 1.43 and 1.74 (based on a historical analysis) because of rampant female infanticide and neglect. With three men for every two women, women were kept uneducated and at home. Sparta, in contrast, was a military state in which males were removed from their families early on to be trained as soldiers. With an extreme shortage of men in Spartan society, girls received educations and even physical training similar to that of boys, and women controlled and inherited property. Fourth century B.C. Spartan women controlled 40 percent of the land and property in Sparta; Athenian women controlled no property at all. But Guttentag’s book was not to be, at least not the way she planned it. On November 4, 1977, just five days short of her 45th birthday, she died from a heart attack while alone in a hotel room in New York City. Her husband, Paul, completed her manuscript, but the book that finally came out in 1983 was academic in nature, not the mainstream “big think” book she intended. With her death, the book deal she had made with a major publisher disappeared, and sex ratio theory stayed mainly in the obscure recesses of various academic specialties. Biologists have looked at the sex ratio in animal populations for generations, typically just by counting the males and females in a pack or herd. The natural sex ratio for the American alligator, for example, is about 0.2, or one male for every five females. That kind of ratio makes sense when males fight a lot and female fertility is low. To study the sex ratio in humans is more challenging, especially if your goal is to determine how the sex ratio affects social systems. Nigel Barber, an evolutionary psychologist based in Birmingham, Alabama, has tested its power more than any other scholar. Among his recent findings: When the sex ratio is low (too many women), women are more slender; when women are in short supply, as was the case in the United States in the 1950s, women are more curvaceous, perhaps because they are trying to look the part of traditional wife and mother. Barber’s studies, which often look at patterns in 40 countries or more, have shown the power of the sex ratio in predicting such things as the rate of nonmarital births, the practice of polygyny, and even the likelihood that men will grow facial hair. The more men there are, he found, the more hair they grow to attract mates. United States Births, 1940-Present In a study of divorces in the U.S. from 1896 to 1992, Barber reports that the divorce rate could be predicted remarkably well from the sex ratio. The success or failure of marriage, in turn, ripples though social systems, affecting prevailing values. When there is an excess of available men—as was true during most of U.S. history because most immigrants are male—marriage is generally revered and values are conservative. When available women outnumber available men, women are set free of the home, and values shift toward liberalism. But a low sex ratio also lowers the living standards of women and causes turmoil in relationships, mainly because men typically have more power in society, which they tend to exercise crudely when there are extra women around. The chaos associated with low sex ratios has been confirmed by several other studies, including a 2010 college-campus investigation by sociologists Jeremy Uecker of Baylor University and Mark Regnerus of the University of Texas at Austin. In a survey of about 1,000 college women, the researchers found that on campuses where women outnumber men, women date less, criticize men more, and are less likely to have a college boyfriend, even though they are also more active sexually. One kind of chaos that seems to flow from a low sex ratio is counterintuitive. In multiple studies that examine this issue both across countries and over time, Barber has shown that a shortage of men is associated with higher rates of rape, violent crime, and assault. When women are in short supply, men compete for resources like good jobs and fancy cars that make them more attractive to potential mates. But when there are too many women, factors such as an absence of fathers from the home and conflict between the sexes act to raise the level of violence. The sex ratio is pushed up or down by many factors, including environmental influences in the womb. A 2010 study conducted in the U.K. found that babies born to two nonsmokers were more likely to be male (birth sex ratio of 1.14), whereas babies born to two smokers were much more likely to be female (birth sex ratio of 0.77). Worldwide, the birth sex ratio is generally above one, about 1.07—nature’s way, perhaps, of compensating for the higher mortality rate of males throughout life. By the time people are in their eighties, however, the sex ratio drops to 0.7 or less. Men are in short supply among the elderly. The sex ratio that is most important in influencing social systems is the one that applies to men and women of mating and child-rearing ages—the availability sex ratio. The fact that women usually prefer marrying men who are slightly older can shift the availability sex ratio up or down almost overnight. This is because the number of people born each year can change dramatically when a war ends or a recession begins. It is this phenomenon, which demographers call the “marriage squeeze,” that led to the enormous excess of available women in the U.S. in the generally liberal 1960s and 1970s. Because of sharp increases in the number of births in the years following World War II and the Korean War, women born two decades later were typically seeking older partners born in years when far fewer babies were born, hence the big drop in the availability sex ratio. So a woman born in 1957, when births were numerous, would, in 1977, be seeking a male born a few years earlier than she—say, in 1954—when far fewer males were born. That’s the “squeeze.” Conversely, birth patterns in the 1970s created an excess of men in the 1990s. In other words, the nationwide shift toward conservatism, and even the election of George W. Bush in 2000, was predictable from sex ratio data. A host of effects produce differences in sex ratios around the world and between racial and ethnic groups. The highest sex ratio in the world right now—4.15—is in Qatar, where thousands of men have immigrated to work on construction and oil projects. The lowest sex ratio—about 0.79—is in Djibouti on the Horn of Africa, where an unemployment rate of 40 to 50 percent has forced men to emigrate. Here in the U.S., African Americans have had a low sex ratio since the era of slavery, in part because they have a low birth sex ratio and in part because many black males are in the military or incarcerated. The absence of men keeps many black women living in poverty, bound to the welfare system. Hispanic Americans, on the other hand, have the highest sex ratio of any ethnic group in the country—over 1.5 for people in their twenties—mainly because far more men immigrate than women. The high sex ratio should make that community politically conservative, yet Hispanics generally support liberal politicians, perhaps because liberal politicians are perceived as more pro-minority and pro-immigrant, overriding the sex ratio influence in this case. In Asian countries, particularly China and India, the ratio of males to females has remained stubbornly and artificially high, causing concern among government officials. Because male offspring are preferred in many Asian cultures, sonograms are now being used to identify female fetuses, which are then aborted in large numbers. The birth sex ratio in China is now an alarming 1.13. The fear in some circles that an excess of men will lead to cultural chaos is actually inconsistent, though, with the views of Secord, Guttentag, and others. Barber’s research suggests, for example, that a high sex ratio generally leads to less violence toward women. But the excess of men in China and India has led to new kinds of abuse—women being abducted from Bangladesh, for example, to serve as brides for single males in India, as well as the trafficking of young women within India. Even the election of George W. Bush in 2000 was predictable from sex ratio data. In relatively stable societies like the U.S., the most powerful factor determining the balance of men and women is that marriage squeeze, and birth patterns over the past 25 years make it possible to estimate the availability sex ratio in the U.S. through the year 2035. The trick here is to determine whether the different numbers of people born each year between 1986 and 2010 are likely to cause marriage squeezes in the future. My computations suggest that we are unlikely in coming years to run into either the liberalism of the ’60s and ’70s (when there were too many women) or the conservatism of the late ’90s (when there were too many men). Instead, we will be trending toward a balance between men and women, and therefore, a prolonged period of moderation in all things political and social: a stable divorce rate, reasonable satisfaction in relationships, and greater gender equality. Absent major natural or human-made disasters that are sex-selective or extreme changes in immigration patterns, the next quarter century should be a time of relative calm. Marcia Guttentag would be pleased. Robert Epstein, senior research psychologist at the American Institute for Behavioral Research and Technology, provided original research for this piece.	3.109375	3	[ 0.0155029296875, -0.00885009765625, 0.0361328125, -0.0181884765625, 0.0078125, -0.010498046875, 0.008544921875, 0.00173187255859375, -0.0184326171875, -0.012451171875, -0.006072998046875, 0.01263427734375, -0.0228271484375, 0.002471923828125, 0.006439208984375, 0.00164031982421875, -0.0194091796875, 0.007415771484375, -0.0087890625, 0.034912109375, -0.0888671875, -0.0011138916015625, -0.01190185546875, 0.007415771484375, 0.036376953125, -0.01251220703125, -0.005279541015625, 0.002716064453125, -0.000904083251953125, 0.01409912109375, 0.00714111328125, -0.0238037109375, -0.0123291015625, -0.0146484375, -0.004119873046875, -0.006866455078125, -0.02490234375, 0.0050048828125, -0.000728607177734375, -0.0135498046875, 0.01483154296875, -0.00604248046875, -0.01287841796875, -0.011474609375, 0.0089111328125, -0.0079345703125, 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Q: There is an error while using System.out.println when both text and variables I am a beginner in Java so I wrote a program to understand the OOP concepts but it gives me an error when trying to use System.out.println(). Here's the code public static void main(String[] args) { sampleClass ADD = new sampleClass(); Scanner input = new Scanner(System.in); int fNum; int sNum; System.out.println("Enter the first number to Add"); fNum = input.nextInt(); System.out.println("Now enter the second number"); sNum = input.nextInt(); int sum; sum = ADD.add(fNum, sNum); System.out.println("The sum of " fNum " and " sNum " is " sum); } A: Replace this line System.out.println("The sum of " fNum " and " sNum " is " sum); with System.out.println("The sum of " +fNum+ " and " +sNum+ " is " +sum); Please Note: In Java, the operator "+" normally acts as an arithmetic operator unless one of its operands is a String. If necessary it converts the other operand to a String before joining the second operand to the end of the first operand. Examples: If one of the operands is not a String it will be converted: int age = 12; System.out.println("My age is " + age);	3.6875	4	[ -0.0089111328125, -0.0162353515625, -0.01708984375, -0.011474609375, 0.018798828125, 0.000591278076171875, -0.00116729736328125, -0.00531005859375, -0.018798828125, -0.0250244140625, 0.00732421875, -0.0206298828125, -0.037109375, -0.020751953125, -0.0206298828125, -0.0069580078125, 0.007354736328125, -0.0208740234375, 0.004150390625, -0.007598876953125, 0.0498046875, -0.0169677734375, -0.00689697265625, 0.002166748046875, 0.0016021728515625, -0.013671875, -0.004547119140625, 0.00714111328125, 0.0169677734375, -0.0022125244140625, 0.0198974609375, -0.00994873046875, 0.01507568359375, 0.03271484375, 0.014404296875, -0.00994873046875, -0.01025390625, 0.0027008056640625, -0.0157470703125, 0.04150390625, 0.0230712890625, -0.02001953125, -0.014404296875, 0.0152587890625, -0.0150146484375, -0.00433349609375, -0.014892578125, -0.005401611328125, 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Geography of Andhra Pradesh Please do not contribute text in a foreign language to English Wikipedia. Your contributions are more than welcome at a Wikipedia in your language. Thank you. Andhra Pradesh lies between 12°41' and 19.07°N latitude and 77° and 84°40'E longitude, and is bordered by Telangana, Chhattisgarh, and Orissa in the north, the Bay of Bengal in the East, Tamil Nadu to the south and Karnataka to the west. Among the other states, which are situated on the country's coastal area, Andhra Pradesh has got a coastline of around 974 km, which gives it the 2nd longest coastline in the nation. Two major rivers, the Godavari and the Krishna run across the state. A small enclave 12 sq mi (30 km²), the Yanam district of Puducherry, lies in the Godavari Delta in the north east of the state. The state includes the eastern part of Deccan plateau as well as a considerable part of the Eastern Ghats. Historically the region comprising the state was known as Andhraapatha, Andhradesa, Andhraavani, and Andhra vishaya. Climate The climate of Andhra Pradesh is generally hot and humid. The summer season in this state generally extends from March to June. During these months the moisture level is quite high. The coastal areas have higher temperatures than the other parts of the state. In summer, the temperature generally ranges between 20 °C and 40 °C. At certain places the temperature is as high as 45 degrees on a summer day. The summer is followed by the monsoon season, which starts during June and continues till September. This is the season for heavy tropical rains in Andhra Pradesh. The major role in determining the climate of the state is played by South-West Monsoons. About one third of the total rainfall in Andhra Pradesh is brought by the North-East Monsoons around the month of October in the state. The winters in Andhra Pradesh are pleasant. This is the time when the state attracts most of its tourists. October to February are the winter months in Andhra Pradesh. Since the state has quite a long coastline, the winters are comparatively mild. The temperature in winter raises from13 °C to 30 °C. Locals and tourists generally find that cotton summer clothes are best suited to coping with the climate of Andhra Pradesh. Divisions Andhra Pradesh can be divided into two regions, namely Coastal Andhra and Rayalaseema. Andhra Pradesh has 13 districts: Anantapur, Chittoor, Kadapa, East Godavari, Guntur, Krishna, Kurnool, Sri Potti Sreeramulu Nellore, Prakasam, Srikakulam, Visakhapatnam, Vizianagaram and West Godavari. Anantapur is the largest district of the state and the 7th largest district in India with an area of 19130 km2. Each district is divided into multiple mandals, and each mandal has many villages. Visakhapatnam is the largest city in the state followed by Vijayawada. Other important cities and towns are Kakinada, Guntur, Rajahmundry, Tirupati, Nellore, Ongole, Kurnool and Eluru. New capital After Telangana was created on 2 June 2014, Andhra Pradesh's erstwhile capital Hyderabad remained in Telangana. Although Hyderabad was set to remain the joint capital of both states for ten years, the new capital is being built at Amaravati only. 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Growers shipping their products to distant places encountered the difficulty of having the live plants arrive both alive and without damage. Damage occurs when the plants, and/or the growing medium, becomes dislodged from the containers. This is especially a problem when the shipping container becomes inverted during transportation. When inverted, the weight of the containers crushes the plants so that upon arrival the plants are no longer usable. The present solution is to offer credits and rebates for the plants damaged during shipping. Previous attempts at shipping live products have included the use of plastic overwrap. This approach has the drawback that live plants need exposure to air and sealing them with plastic does not allow respiration necessary for live plants. Another approach has been to use a plastic netting to hold the plants within their containers. Netting has proved insufficient in that plants are still able to fit within holes in the netting and become damaged. There is a need in the art for a system for shipping live plants that protects plants from becoming dislodged from their containers and prevents crushing of the plants if the container becomes inverted during shipping. It is an object of the invention to provide a system for shipping live plants. It is another object of the invention to provide a covering for plants within containers maintaining the plant within the container but allowing for respiration. It is another object of the invention to provide a shipping system preventing crushing of plants when the shipping container is inverted. It is another object of the invention to provide a shipping system for live plants minimizing the loss of plants during shipping. It is still another object of the invention to provide a shipping system which is simple and inexpensive to use. It is yet another object of the invention to provide a shipping system for live plants that safely ships a multitude of plants simultaneously. These and other objects of the invention will become apparent to one of ordinary skill in the art after reviewing the disclosure of the invention.	3.1875	3	[ -0.010009765625, -0.00201416015625, 0.00872802734375, -0.0072021484375, -0.0023345947265625, -0.0235595703125, 0.0157470703125, 0.002777099609375, -0.0135498046875, 0.006011962890625, 0.004730224609375, 0.01239013671875, -0.0257568359375, -0.009033203125, -0.00167083740234375, 0.003936767578125, -0.0025634765625, -0.02294921875, 0.0172119140625, -0.00095367431640625, 0.047119140625, -0.0040283203125, -0.00066375732421875, 0.00726318359375, 0.01202392578125, -0.016357421875, -0.00091552734375, 0.0014801025390625, -0.0164794921875, -0.00148773193359375, -0.00067901611328125, 0.007537841796875, -0.0283203125, 0.0152587890625, 0.002197265625, -0.0123291015625, 0.0120849609375, -0.0076904296875, -0.001251220703125, -0.031494140625, -0.0024871826171875, -0.0031585693359375, -0.0196533203125, 0.020263671875, -0.01409912109375, 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Spatial distribution and temporal variability of arsenic in irrigated rice fields in Bangladesh. 2. Paddy soil. Arsenic-rich groundwater from shallow tube wells is widely used for the irrigation of boro rice in Bangladesh and West Bengal. In the long term this may lead to the accumulation of As in paddy soils and potentially have adverse effects on rice yield and quality. In the companion article in this issue, we have shown that As input into paddy fields with irrigation water is laterally heterogeneous. To assess the potential for As accumulation in soil, we investigated the lateral and vertical distribution of As in rice field soils near Sreenagar (Munshiganj, Bangladesh) and its changes over a 1 year cycle of irrigation and monsoon flooding. At the study site, 18 paddy fields are irrigated with water from a shallow tube well containing 397 +/- 7 microg L(-1) As. The analysis of soil samples collected before irrigation in December 2004 showed that soil As concentrations in paddy fields did not depend on the length of the irrigation channel between well and field inlet. Within individual fields, however, soil As contents decreased with increasing distance to the water inlet, leading to highly variable topsoil As contents (11-35 mg kg(-1), 0-10 cm). Soil As contents after irrigation (May 2005) showed that most As input occurred close to the water inlet and that most As was retained in the top few centimeters of soil. After monsoon flooding (December 2005), topsoil As contents were again close to levels measured before irrigation. Thus, As input during irrigation was at least partly counteracted by As mobilization during monsoon flooding. However, the persisting lateral As distribution suggests net arsenic accumulation over the past 15 years. More pronounced As accumulation may occur in regions with several rice crops per year, less intense monsoon flooding, or different irrigation schemes. The high lateral and vertical heterogeneity of soil As contents must be taken into account in future studies related to As accumulation in paddy soils and potential As transfer into rice.	3.203125	3	[ 0.01373291015625, 0.01373291015625, 0.00494384765625, -0.006561279296875, 0.0177001953125, -0.0126953125, 0.005462646484375, -0.02099609375, 0.01611328125, 0.004638671875, 0.0028076171875, 0.0245361328125, -0.0419921875, -0.0140380859375, -0.0133056640625, -0.01153564453125, -0.00701904296875, 0.0025177001953125, -0.002777099609375, -0.000274658203125, -0.00714111328125, 0.00970458984375, -0.00616455078125, 0.00799560546875, -0.0155029296875, -0.002532958984375, 0.00482177734375, -0.024658203125, -0.00933837890625, -0.0177001953125, -0.002716064453125, 0.004547119140625, -0.01007080078125, 0.0036163330078125, 0.0242919921875, 0.01385498046875, 0.00604248046875, -0.007568359375, 0.00494384765625, 0.00811767578125, 0.00213623046875, -0.005401611328125, -0.0098876953125, 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Poverty in America: Social Changes & Global Crises Looking at poverty in the American continent is essential to better understand how the former colonies have evolved into radically different countries. Country by country, analyzing the social and economic paths taken, we can see the effects of discrimination, land ownership, wealth distribution & corruption. If you want to read more on the origins of the huge wealth differences between North America and South America, we recommend the article on the causes of poverty. USEFUL LINKS Poverty in America: The United States ‍Homelessness in the United States Historical overview From the 1950s to the early 1970s, poverty in America (i.e. USA) fell continuously as the economy was booming and the average income was rising. This led to a total elimination of absolute poverty in the country. But at the turn of the 21st century, over 1 in 10 American was poor, 20% of whom where African Americans. The reason for this is that when the 1970s oil crisis hit the USA, poverty climbed up again, only to go down again in the 1990s with the new economic boom. Market liberalization in this mature economy brought more efficiency, while other American developing economies were suffering of its impact. The rise of urban poverty in America The 1970s and 1980s decades are also times when poverty in America became concentrated in urban areas, in particular the old, charming industrial centers. At the same time the population also started to change with the arrival of more and more immigrants from Latin America, reshaping the face of poverty. Urban poverty then tripled in ten years and kept on its expansion onto the 1980s decade. It’s now one of the main features of poverty in America (country and continent). As of 1980, nearly 70% of the urban poor were black, 20% were Latinos, and 10% white. A new face of poverty: immigration and single moms Another thing that changed: the traditional family structure. Like it or not, things have changed and you won’t force an unhappy woman to stay married to her husband anymore. Although, some governments actually tried to by restricting welfare support to families headed by a married couple (talk about government intervention!). Well, that wasn’t the official goal but it was clearly the effect. And millions of single mothers were dropped from welfare support. Demographic changes (immigration) as well as changes in the family structure have had a massive impact on poverty in the US for a couple of decades until things finally stabilized. Now their effect is minor, even though immigrants and single mothers (and their kids) still represent much of the poor. But in a stable way, i.e. the numbers don’t change too much. Yey. Oh no, that’s without counting on the effects of the latest economic crisis! Is poverty in the US completely fake? It’s the old “oh when I was a kid we didn’t have TV nor a microwave oven”. But judging today’s poor on 1970s criteria is just completely absurd because we don’t live like we used to in 1970s. Prices are different, education costs hell of a lot more, living standards and norms are totally different. This means that they simply don’t know the definition of poverty. Speaking of absolute poverty in developed countries is just ridiculous, relative poverty is what matters, in other terms, the capability to fully participate in the life of the nation (having a job, having the Internet and whatnot). Of course the poor today live better than the average in the 1950s, but back then they also used to die of diseases and cancers you can now cure. And today you also need to pay for that somehow. US poverty line and US welfare In comparison to other rich countries, the US ranks usually pretty high in the poverty charts (not a good thing). That’s mostly because of the children and the elderly, who fall disproportionately below the poverty line compared to other groups. Time to get a job, kids. The problem is that in most advanced economies child poverty is usually less than 10% whereas in the US it’s been around 20%. It even rose to 25% recently and the country currently counts 1 in 4 children on food stamps. Good days are gone, baby, gone. Another characteristic of American poverty is the living condition of impoverished single parents – usually moms – who even while they work more than their counterparts in Europe or Australia receive less transfer benefit than in other countries. Since their low paid jobs aren’t enough to maintain the household above the poverty line… well they just fall below that line and make do with poorness. But, this also has some positive impacts on the American economy that lead to an interesting debate. Do you want less inequality or a more competitive economy? Is a middle ground possible? Are there other forms of riches non-measurable in dollars? As far as poverty in America goes, you won’t find all the answers right now (probably not before a decade), but here you can start finding out more on US welfare and the national poverty level. Read more about the national poverty level and US welfare. Meanwhile in Canada ‍A beggar in Canada Income inequalities Looking at the recent history of poverty in Canada you can see that income inequalities have increased from 1980 to 2000, especially during the recession of the early 1990s while a huge surge in immigration brought wages down at a bad time. There were big disparities between, say, retirees who were enjoying a pension greater than ever before and immigrants and industrial workers who generated for the first time concentrated urban poverty in the country. The high level of income of older Canadians hid as well just how poor young workers were by bringing up the average income nationwide. Thus in the 1990s the ones witnessing the most inequalities were the young and the single, who were increasingly unemployed… until the good times came back. Immigrants were facing very low income too, but proportionately speaking they weren’t yet that many and most of the urban poor was still white. Canadian poverty and major transformations The reason that inequalities are important in Canada is that they underline the transformations of the economy and the society. These changes put a lot of pressure on how to best redistribute public resources from health care to housing support in the population. Urban poverty – when over 40% of residents in an area live below the poverty line – indeed appeared in the 1980s in an extensive way throughout the country and has had severe consequences on welfare provision, access to education and the rise of unemployment. Ethnic groups were particularly affected by the phenomenon but since the majority of the urban poor was white nonetheless it hinted at the fact that the problem was structural (rather than discriminative): the job market and the economy. Poverty in America: the Latin side of things ‍Poverty in Latin America Absolute or relative? Poverty in Latin America has always been somewhere in-between: neither completely absolute poverty nor completely relative poverty. What does this mean? On this side of the continent, poverty in America meant not having access to many basic services such as primary health care, education, sometimes also water or electricity, but food for instance hasn’t been that big of an issue. In 1980 only 15% of the population was concerned by malnutrition while almost 50% of Africa and South Asia were. Malnutrition in Latin America However, here again we’re being tricked by the numbers and the averages. Many Latin American countries have had a mostly urban population (over 50%) where food supply isn’t usually a problem. But as of 1980 there were still quite a few that were mostly agrarian societies, where food poverty tends to be higher. Therefore, while the average says that “only” 15% of people lack food in Latin America, this masks the fact that in some countries only 1% of the population suffered from malnutrition while in other neighboring countries it went as high as 50%. Even then, it also depended on the definition of urban area, which is prone to pretty incredible variations across the globe. Whether you include slums and Brazil-style favelas or not makes quite a difference. Slums residents often lack food as well, and on top of that they’re totally cut off from the rest of the population and thus lack access to the most elementary services that provide decent living conditions. Rural poverty in Latin America Yet, in the end absolute poverty in Latin America is mostly rural. In such areas, a radical difference with the development of Northern American countries is that landowners have traditionally made up only 5% of the population (against 70 to 80% in the US and Canada a century ago) and this has dramatically shaped the way Latin American countries have developed with embedded inequalities in their societies. The amount of land that farmers possess nowadays still affects how much food they get and the extent of poverty in America, south of the Rio Grande. It determines whether or not they’ll live below the poverty line. Also, read about poverty in Haiti, and what makes it an exception in Latin America Poverty in Mexico: an American classic? ‍Poverty in America: the main cause of immigration to the US & Canada Very rich and yet very poor Over 40 million people live in poverty in Mexico (that’s about 40% of the population), among whom some 15 million live in extreme poverty, as defined by the World Bank (less than $1.25/day). Strangely, Mexico nonetheless is a pretty rich country – 13th economy in the world – which shows that high GDP doesn’t necessarily mean less poverty, for example if there’s no redistribution whatsoever of the country’s riches. What’s more, having such a high poverty rate puts a huge strain on the economy and hurts the country’s competitiveness (natural correlation between poverty and the economy). This much is one typical aspect of poverty in America where many rich countries have maintained inequalities inherited from the colonial era. As only a few rip the benefits of Mexico’s opportunities and resources (and don’t reinvest their capital in the country), the rest of the economy shrinks, unemployment grows and wages go down. The fault goes directly to Mexico’s rich for making poverty worse. That’s the old story of poverty in America on the Latin side. Poverty and economic crises Now in fact Mexico wasn’t doing too bad until the 1980s. Before that inflation was under control, productivity was rising year by year and GDP per capita used to grow by 3-4% every year. But then in the early 1980s came the economic crisis that hit Mexico and Brazil so hard it devastated their economy. Up to now, all Mexican policies do is still try to fix the consequences of what happened decades ago. At that time the peso suffered a major devaluation, inflation skyrocketed (between 100% to 150%, while you can say that 2-5% is okay/normal), wages plummeted by as much as 40% and public debt rose to over 100% of GDP. Facing that much poverty, millions of Mexicans obviously started migrating to the US and Canada at the same time, as mentioned before. Mexico is a perfect example of how poverty, economic cycles and macro-economy can be intimately connected. Cuba, the black sheep of American poverty A strange case After years of struggle Cuba became in 1959 (officially 1961) an independent socialist country, allegedly fulfilling the dreams of its revolutionary leaders. Now Cuba is a strange spot in the story of poverty in America because in many ways it can’t be considered poor. In many ways it fairs better than many advanced economies in terms of equality and quality of services it offers its population. Yet, both the population and the state are becoming penniless which puts the whole system at risk. As the country is running broke and was hit hard by the 2008 economic crisis, there is a dire need for profound reforms and changes in the economy. Historical review of Cuba and its poverty levels For the 30 years following its independence Cuba’s GDP rose by 4% per year, even though 20 to 30% of its GDP was in fact made of aid coming from the USSR. But in the end Cuba boasts today an HDI (Human Development Index) of 0.8, one of the highest in the developing world. The reason for such high HDI is that the index gives great importance to access to education and health care, and Cuba happens to offer universal access to both. So, a healthy and very well educated workforce… but there are no jobs to up to the local level of education. Sounds like the perfect definition of waste of talent and “human capital”. The challenge for Cuba, as you’ll have understood, is to adapt to this post-soviet world of ours and handle the transition and reforms that have recently caused waves of inequalities. But Cuba also holds a few keys regarding how poverty in America can best cope with issues related to globalization and liberalization, which have brought massive inequalities to the whole continent. These content links are provided by Content.ad. 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It is particularly preferred to employ Staphylococcal genes and gene products as targets for the development of antibiotics. The Staphylococci make up a medically important genera of microbes. They are known to produce two types of disease, invasive and toxigenic. Invasive infections are characterized generally by abscess formation effecting both skin surfaces and deep tissues. S. aureus is the second leading cause of bacteremia in cancer patients. Osteomyelitis, septic arthritis, septic thrombophlebitis and acute bacterial endocarditis are also relatively common. There are at least three clinical conditions resulting from the toxigenic properties of Staphylococci. The manifestation of these diseases result from the actions of exotoxins as opposed to tissue invasion and bacteremia. These conditions include: Staphylococcal food poisoning, scalded skin syndrome and toxic shock syndrome. SpoIIIE is a membrane bound protein involved in chromosome partitioning during sporulation and vegetative replication in a wide variety of bacteria. The SpoIIIE gene was initially characterised in Bacillus subtilis (Butler P. D. and Mandelstam J. (1987) Journal of General Microbiology 133:2359-2370). SpoIIIE protein has an ATP binding site and is membrane-bound, and appears to form a pore in the nascent spore septum, through which the prespore chromosome is driven in a conjugation-like mechanism (Wu L. J., Lewis P. J., Allmansberger R., Hauser P. M. and Errington J. (1995) Genes and Development 9:1316-1326). spoIIIE mutants cannot sporulate as they are unable to partition the prespore chromosome into the polar prespore compartment. Instead a specific chromosomal segment comprising approximately 30% of the chromosome enters the prespore, while the rest remains in the mother cell, trapped by the septum (Wu L. J. and Errington J. (1994) Science 264:572-575). In wild-type cells SpoIIIE is membrane-bound, and appears to form a pore in the nascent spore septum, through which the prespore chromosome is driven in a conjugation-like mechanism (Wu L. J., Lewis P. J., Allmansberger R., Hauser P. M. and Errington J. (1995) Genes and Development 9:1316-1326). It has been shown that SpoIIIE is also required for correct partitioning of the B.subtilis chromosome during vegetative cell division. spoIIIE- Mutants in which replication has been artificially delayed are unable to separate the replicated chromosomes before septum formation, resulting in a trapped nucleoid similar to that formed at the start of sporulation (Sharpe M. E. and Errington J. (1995) Proceedings of the Natural Academy of Sciences USA 92:8630-8634). SpoIIIE has been shown to be essential in Escherichia coli (Begg K. J., Dewar, S. J. and Donachie W. D. (1995) Journal of Bacteriology 177:6211-6222). Highly conserved SpoIIIE homologues are found in diverse members of the eubacteria such as Campylobacter jejuni (Miller, S., Pesci E. C. and Pickett C. L. (1994) Gene 146:31-38), Coxiella burnetii (Oswald W. and Thiele D. (1993) Journal of Veterinary Medecine B40:366-370), Eshcerichia coli (Begg 1995 above) and Haemophilus influenzae (Fleischmann, R. D., Adams, M. D., White, O., Clayton, R. A., Kirkness, E. F., Kerlavage, A. R., Bult, C. J., Tomb, J.-F., Dougherty, B. A., Merrick, J. M., McKenney, K., Sutton, G., FitzHugh, W., Fields, C. A., Gocayne, J. D., Scott, J. D., Shirley, R., Liu, L.-I., Glodek, A., Kelley, J. M., Weidman, J. F., Phillips, C. A., Spriggs, T., Hedblom, E., Cotton, M. D., Utterback, T. R., Hanna, M. C., Nguyen, D. T., Saudek, D. M., Brandon, R. C., Fine, L. D., Fritchman, J. L., Fuhrmann, J. L., Geoghagen, N. S. M., Gnehm, C. L., McDonald, L. A., Small, K. V., Fraser, C. M., Smith, H. O. and Venter, J. C. (1995) Science 269:496-512). All of these proteins are 36-55% identical at the amino acid level overall. Their N-terminal 200 amino acids are hydrophobic and not conserved, so if the C-terminal 500 or so amino acids are considered alone the level of conservation rises to 42-67% identical amino acids. This high level of identity among diverse eubacteria strongly suggests commonality of function. Inhibitors of SpoIIIE proteins would prevent the bacterium from establishing and maintaining infection of the host by preventing it from correctly partitioning the chromosome in the manner described above and thus arresting cell division and growth, rendering the bacterium susceptible to host defences and leading ultimately to cell death and thereby have utility in anti-bacterial therapy. Clearly, there is a need for factors that may be used to screen compounds for antibiotic activity and which factors may also be used to determine their roles in pathogenesis of infection, dysfunction and disease. There is also a a need for identification and characterization of such factors and their antagonists and agonists which can play a role in preventing, ameliorating or correcting infections, dysfunctions or diseases. The polypeptides of the invention have amino acid sequence homology to a known B. subtilis spoIIIE protein.	3.140625	3	[ -0.02099609375, 0.0247802734375, 0.018310546875, -0.0062255859375, -0.019287109375, -0.0380859375, -0.0023956298828125, -0.007110595703125, -0.005523681640625, 0.00921630859375, 0.01153564453125, 0.0111083984375, -0.0272216796875, 0.00604248046875, -0.006805419921875, -0.0089111328125, 0.0002651214599609375, -0.00518798828125, -0.0233154296875, -0.000812530517578125, 0.0213623046875, 0.002655029296875, -0.00103759765625, 0.0135498046875, -0.017333984375, 0.003814697265625, 0.000202178955078125, 0.01470947265625, 0.0012969970703125, 0.01129150390625, -0.000766754150390625, -0.0010223388671875, -0.00836181640625, -0.00238037109375, 0.0032806396484375, -0.01556396484375, 0.0087890625, -0.0093994140625, 0.002105712890625, -0.000797271728515625, -0.01177978515625, -0.001739501953125, -0.0133056640625, 0.0089111328125, -0.005950927734375, -0.00013446807861328125, 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Since the first US case of coronavirus disease 2019 (COVID-19) infection as identified in Washington State on January 20, 2020, more than 235 000 cases have been identified across the US in just over 2 months. Given the challenges in expanding testing capacity and the restrictive case definition of persons under investigation, the true number of cases is likely much higher. By March 17, the outbreak had expanded from several isolated clusters in Washington, New York, and California to all 50 states and the District of Columbia. As of April 2, there have been more than 5000 COVID-19–associated deaths in the US. With a global total now of more than 1 million cases, the US is now the country with the largest number of reported cases, comprising about one-fifth of all reported infections. With community transmission firmly established, the US epidemic enters the exponential growth phase in which the number of new cases is proportional to the existing number of cases. This phase continues until either enough susceptible individuals become immune as a result of infection, stringent public health measures are followed, or both. Case Fatality A yet unanswered question that adds to uncertainty around the outbreak involves the case-fatality rate (CFR), defined as the percentage of deaths among all cases. Presently, global mortality is reported at 4.7% but this varies widely by location from a high of 10.8% in Italy to a low of 0.7% in Germany. Several factors influence the CFR including a reliable estimate of the total number of cases. Among the first 140 904 cases in the US, 1.7% died; however, given the uncertainty in the denominator, this is not a reliable CFR estimate. For example, the crude CFR in Wuhan, China, was reported to be 5.8% on February 1, whereas more methodologically robust estimates using novel methods to estimate the actual number of cases reported the CFR as 1.4%.1 In the coming weeks, surge capacity at US hospitals will influence the CFR. However, to have reliable estimates, better approximations of the overall population (denominator) are essential, and methods such as serosurveys using statistical sampling generalizable to the populations of interest will inform these estimates. New Clinical and Epidemiological Insights Is PCR Always Positive? What Is the Meaning of a Negative PCR? Several types of tests are being used to identify severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).2 These can be classified into 2 general categories: molecular diagnosis/polymerase chain reaction (PCR)–based testing and serological testing. In clinical settings, PCR-based testing remains the primary method of identifying SARS-CoV-2. Given the lack of a reference standard for diagnosing COVID-19, the sensitivity and specificity of diagnostic testing are unknown. In addition, inadequate sample collection may reduce test sensitivity. In a study of 5 patients, individuals with chest computed tomography findings compatible with COVID-19, and a negative reverse transcriptase (RT)–PCR result for SARS-CoV-2, tested positive on subsequent testing, suggesting that certain patients (eg, with compatible radiological findings) might require repeat testing with specimens collected from multiple sites in the respiratory tract.3 It is likely that lower respiratory samples (eg, minibronchial alveolar lavage) are more sensitive than a nasopharyngeal swab. Thus, it is important to emphasize that, depending on the clinical presentation, a negative RT-PCR result does not exclude COVID-19. Multiple serological tests are in various stages of development. With wider availability of serological testing, it will be possible to determine whether patients have a false-negative PCR result. Can Patients Become Reinfected? Reports from China and Japan have indicated that some patients with COVID-19 who were discharged from the hospital after a negative RT-PCR result were readmitted and subsequently tested positive on RT-PCR. It is unclear from the available information if these were true reinfections or the tests were falsely negative at the time of initial discharge. However, while other coronaviruses demonstrate evidence of reinfection, this usually does not happen for many months or years. Therefore, it is unlikely that these were true cases of reinfection. Some reassuring evidence comes from a challenge study among rhesus macaques.4 After initial challenge and clearance of SARS-CoV-2, the animals were rechallenged with the virus but were not infected. While the evidence on reinfection is evolving, current data and experience from previous viruses without substantial seasonal mutation do not support this hypothesis. How Long Does Immunity Last? Presently, there is no validated immune correlate of protection for SARS-CoV-2, ie, antibody level or another immunological marker associated with protection from infection or disease. However, in a study that included 82 confirmed and 58 probable cases of COVID-19 from China, the median duration of IgM detection was 5 days (interquartile range, 3-6), while IgG was detected at a median of 14 days (interquartile range, 10-18) after symptom onset.5 Because the outbreak is only a few months old, there are no data on long-term immune response. Data from SARS-CoV-1 indicate that titers of IgG and neutralizing antibodies peaked at 4 months after infection, with a subsequent decline through at least 3 years after infection. Should Everyone Wear a Mask in Public? Current guidelines from the Centers for Disease Control and Prevention (CDC) do not recommend routine use of medical masks among healthy individuals and suggest limiting mask use to health care workers and those caring for patients with COVID-19. However, this guidance is likely to be modified. Regardless, any change in policy should prioritize the availability of masks for health care workers. Priority should also be given to others with risk of exposure such as first responders and incarcerated individuals. Due to the current scarcity of masks, many in the community have begun sewing masks for themselves and for health care workers. A fitted N95 respirator is the preferred type of medical mask for health care workers; however, supplies in the US are very limited. Medical masks are also recommended for symptomatic individuals to prevent them from transmitting the virus. The rationale supporting the recommendations comes from studies finding limited to no efficacy of masks in protecting healthy individuals from influenza infection and also for the need to preserve supplies. However, evidence from influenza studies might not be relevant for COVID-19. For example, in a systematic review, masks, particularly combined with other measures such as handwashing, were found to be effective in preventing SARS-CoV-1 infection.6 Moreover, with the increasing evidence of presymptomatic transmission of SARS-CoV-2, there might be value in the use of masks among individuals at risk of transmission.7 How Does SARS-CoV-2 Spread? Current evidence suggests that SARS-CoV-2 is primarily transmitted through droplets (particles 5-10 μm in size). Person-to-person transmission occurs when an individual with the infection emits droplets containing virus particles while coughing, sneezing, and talking. These droplets land on the respiratory mucosa or conjunctiva of another person, usually within a distance of 6 ft (1.8 m) but perhaps farther.8 The droplets can also settle on stationary or movable objects and can be transferred to another person when they come in contact with these fomites. Survival of the virus on innate surfaces has been an important topic of discussion. While there are few data, the available evidence suggests that the virus can remain infectious on inanimate surfaces at room temperature for up to 9 days. This time is shorter at temperatures greater than 30° C. The good news is that cleaning and disinfection are effective in decreasing contamination of surfaces, emphasizing the importance of high-touch areas.9 Transmission through aerosols, particles smaller than 5 μm, can also occur under specific circumstances such as endotracheal intubation, bronchoscopy, suctioning, turning the patient to the prone position, or disconnecting the patient from the ventilator. Cardiopulmonary resuscitation is another important aerosol-generating procedure. In a recent study of environmental sampling of rooms of patients with COVID-19, many commonly used items as well as air samples had evidence of viral contamination.10 In the context of the heterogeneity in evidence and possibility of aerosolization of the virus during certain medical procedures, public health agencies (including the CDC) recommend airborne precautions in situations involving patients with COVID-19. When Can Social Distancing Measures Be Lifted? With the exponential increase in US COVID-19 cases and deaths, several jurisdictions have implemented social-distancing measures. Modeling and empirical studies suggest that social-distancing measures can help reduce the overall number of infections and help spread out cases over a longer period of time, thus allowing health systems to better manage the surge of additional patients. However, long-term social distancing can have detrimental effects on physical and mental health outcomes as well as the economy. A few changes may allow for easing restrictions: First, an aggressive program of testing to identify asymptomatic and mild cases combined with proactive contact tracing and early isolation as well as quarantine of contacts. Second, there must be a focus on reducing home-based transmission. In Wuhan, particularly after the initial phase, most transmissions occurred within households. While the CDC has published guidelines for preventing household transmission, it did not place enough emphasis on the importance of having the infected person always wear a mask. Third, even a treatment that only shortens an intensive care unit stay by 20% to 30% can have a substantial benefit on health system capacity. When Will a Vaccine Be Available? The ultimate strategy for controlling this pandemic will depend on a safe and efficacious vaccine against SARS-CoV-2. However, only 3 vaccine candidates are currently in phase 1 human trials: a messenger RNA vaccine and 2 adenovirus vector-based vaccines. The estimated timeline for availability of an initial vaccine is between early and mid-2021. Conclusions As the COVID-19 outbreak expands in the US, overall understanding of this disease has increased, with more information available now than even a few weeks ago. However, more evidence is needed, particularly for public health and clinical interventions to successfully prevent and treat infections. Even during a pandemic, obtaining rigorous, reliable data is not a distraction, rather it is essential for accurately measuring the extent and severity of COVID-19 and assessing the effectiveness of the response. Back to top Article Information Corresponding Author: Carlos del Rio, MD, Emory University School of Medicine, 49 Jesse Hill Jr Dr SE, FOB Room 201, Atlanta, GA 30303 (cdelrio@emory.edu). Published Online: April 6, 2020. doi:10.1001/jama.2020.5788 Conflict of Interest Disclosures: Dr del Rio reported receiving grants from the National Institutes of Health/National Institute of Allergy and Infectious Diseases. 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Materials scientists have created a substance called 'new diamond.' It has the hardness of diamonds, without one of their very significant weaknesses. Unfortunately, the 'new diamonds' don't have their advantageous sparkle either. Learn about the strength behind diamond's 'ugly stepsisters.' Diamond is one of the hardest substances in the world. It's able to withstand scratching and pressure and incredible shocks, or at least that's what we've been told. Although diamonds have been held up as an amalgamation of strength and beauty, their beauty is actually their weakness. They're crystals. A crystal is formed when atoms, in this case carbon atoms, are locked into a repeating structure. The structure is patterned, but it is not symmetrical in every direction. Hit the structure one way and it's hard as, well, a diamond. Hit it another way and it has only a small fraction of the hardness. Enter 'new diamond.' This material is created from a material first made in the 1950s called 'glassy carbon.' Glassy carbon is a hard, difficult-to-melt, glass-like substance that's often used because of its durability. Compress that to 400,000 times atmospheric pressure and you create the dark, slightly shiny material of new diamond. It can take 1.3 million times atmospheric pressure, a feat only matched by diamonds. Unlike diamonds, new diamond is not a crystalline structure but an amorphous material - aka a blob. Since its molecules are oriented any which way, they can be hit any which way and stand up to the same pressure. And what will scientists do with this new wonder material? The first idea is to make new diamond into an anvil, on which they can make even denser and harder materials.	3.625	4	[ 0.000827789306640625, -0.01043701171875, -0.00531005859375, 0.0089111328125, -0.01361083984375, -0.01220703125, 0.0022430419921875, -0.008056640625, 0.00124359130859375, 0.0086669921875, 0.0164794921875, 0.01116943359375, 0.0126953125, 0.01080322265625, -0.004302978515625, -0.00019741058349609375, 0.01397705078125, 0.006134033203125, 0.0087890625, 0.00518798828125, 0.0322265625, -0.01483154296875, -0.00897216796875, 0.007476806640625, 0.000560760498046875, -0.003265380859375, -0.00016117095947265625, -0.00098419189453125, -0.0006103515625, 0.003509521484375, 0.0079345703125, 0.006561279296875, -0.0224609375, 0.000896453857421875, 0.00008678436279296875, 0.0009765625, 0.01226806640625, 0.00013065338134765625, -0.015625, -0.01019287109375, -0.0162353515625, 0.0084228515625, 0.00193023681640625, 0.021484375, 0.007080078125, 0.00811767578125, 0.01226806640625, 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Lake Baikal, in eastern Siberia, is no ordinary lake. Here are some interesting facts about it: » Lake Baikal is the deepest lake in the world with a maximum depth of 1,632m » It is also the world’s largest volume of fresh water 23,000 cubic km. » This means that one-fifth of all the fresh water in the world is located here at Lake Baikal. » Lake Baikal is 640km long and judging by its dimensions only it would be more of a sea than a lake. » Baikal is also the world’s most ancient freshwater lake, it originated 20-25 million years ago. » It is home to many unique species of animals and plants including the freshwater seal. » Lake Baikal is one of the clearest and purest bodies of water. In a good day you could see 40 meters into the lake. » Dimensions of Lake Baikal: It is 636 km long, 79 km wide. » There are 27 islands in Lake Baikal, most of them being uninhabited. » Baikal Lake’s coastline measures 2100 kilometers (around 1300 miles). » More than 300 streams and rivers flow into Lake Baikal, but there is just one outlet, the Angara. » The water in the lake creates a mild microclimate around its shores. » More than half the species found in Lake Baikal are unique to this place.	3.53125	4	[ 0.004241943359375, -0.00958251953125, 0.0233154296875, 0.01348876953125, -0.01483154296875, -0.013427734375, 0.008056640625, -0.006378173828125, 0.001617431640625, -0.011474609375, 0.000873565673828125, 0.0194091796875, -0.0289306640625, -0.01239013671875, -0.00897216796875, 0.005218505859375, -0.0081787109375, -0.01708984375, 0.0111083984375, 0.007110595703125, 0.018798828125, -0.00469970703125, -0.0146484375, 0.00933837890625, -0.01483154296875, -0.018798828125, -0.008056640625, 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Over the past several decades, substantial effort has been invested in the design and development of improved internal combustion engines. Design efforts have been, directed toward the creation of smaller, lighter engines with improved fuel efficiency and power. Engines have been characterized by their method of combustion, e.g., compression (diesel) or spark-ignited (gasoline). Further, engines are described and identified by the orientation and/or number of their pistons and cylinders, e.g., V-8, in-line 6, radial, Wankel rotary, horizontal and horizontally-opposed. Internal combustion engines with horizontally-oriented pistons and cylinders have been the subject of much research over the past several decades. Their inherent low profile offers an opportunity to reduce engine size while maintaining fuel efficiency and power. Various countries have introduced several variations of both four cylinder and six cylinder horizontally-oriented engines. A typical horizontally-oriented engine configuration includes multiple pairs of horizontal cylinders with a separate piston slidably disposed in each separate cylinder. The top or "crown" of each piston, in combination with the cylinder walls and a separate cylinder head, forms a unique, single combustion chamber. Each cylinder head, also provides a separate surface for intake and exhaust valve assemblies. In the case of spark-ignited engines, each cylinder head also provides a port for installation of some means for igniting the combustible mixture, usually a spark plug. For a typical horizontally oriented engine, each piston is connected to a common crankshaft. During operation, a mixture of air and fuel is introduced into each combustion chamber. The mixture is then combusted, by either compression (diesel engines) or a spark (gasoline engines). When combusted, the energy generated by the exothermic expansion of the combustible mixture serves to drive the piston away from the cylinder head. In so doing, the piston's linear kinetic energy is delivered to the engine's crankshaft by a connecting rod rotatably attached to the piston. The crankshaft then delivers rotational power to the power train. Several patents have offered modifications to the typical horizontally-oriented piston and cylinder configuration. Most notably, and of relevance to the present invention, is that prior art which teaches horizontally-oriented engine configurations with one combustion chamber shared between two or more pistons/cylinders. Generally, these types of engines are known as horizontally-opposed engines. For example, Henry (U.S. Pat. No. 1,533,004) teaches an internal combustion engine with a combustion chamber shared between two cylinders. The shared combustion chamber is formed by the walls of two interconnected cylinders, the crowns of two opposing pistons which slidably reciprocate within the cylinders, and a single cylinder head. In addition to acting as a wall of the shared combustion chamber, the cylinder head provides a surface for intake and exhaust ports as well as spark plug access. In Henry, the pistons simultaneously converge toward each other and then simultaneously diverge away from each other during the various engine cycles. Other patents, including most notably Feeback (U.S. Pat. No. 3,485,221), Rassey (U.S. Pat. No. 4,244,338), Johnson (U.S. Pat. No. 4,554,894) and Honkanen (U.S. Pat. No. 5,133,306) have proposed variations on the horizontally-opposed engine configuration. Each of the above include intake and exhaust valve assemblies which are located to the side of each cylinder pair. Consequently, as with Henry discussed above, these engines all require at least one separate cylinder head per cylinder pair. Other relevant prior art teaches internal combustion engines with shared combustion chambers, but whose converging pistons are not horizontally-oriented. For example, Ascari (U.S. Pat. No. 5,447,818) teaches an engine with at least four cylinders that form two separate shared combustion chambers. Two cylinders and pistons are oriented at angles of approximately ninety degrees to each other, with the crown of each piston oriented toward a shared plane of symmetry. Ascari likens his engine to a "superimposed twin V." Again, the shared combustion chamber is formed by the cylinder wall, two piston crowns and a single cylinder head. The prior art clearly evidences that the ability to reduce the overall size and weight of opposed piston engines with shared combustion chambers has been hampered by the need to include a suitable surface, i.e. a cylinder head, to accommodate the shared intake and exhaust valve assemblies. As previously indicated, in engines without shared combustion chambers, each cylinder has a cylinder head which provides a surface for the valve assemblies. Engines with shared combustion chambers have generally provided for the placement of the shared intake and exhaust valve assemblies in a separate "cylinder head-like" element that is separately bolted to the side of the cylinder blocks. The present invention advances the prior art by eliminating the need for a separate cylinder head. Although the prior art teaches reduction in the number of required cylinder heads for dual piston/cylinder engine configurations from two to one, it still struggles with valve design and placement. The intake and exhaust valve assemblies are typically located between the ends of the dual cylinders to serve a common or shared combustion chamber. Consequently, this additional space requirement frequently limited the ability to bring the ends of the cylinders, and hence, the crowns of the pistons, closely together. The patent to Rassey specifically teaches that "previous attempts to adapt poppet valves [in horizontally-opposed engines] have proven largely unsuccessful since the poppet valves cannot be positioned above the piston head as in the more conventional internal combustion engines." Accordingly, a need exists for a cylinder/piston configuration of simple and reliable design which includes a combustion chamber shared between two horizontally-opposed cylinder/piston assemblies, yet allows the use of poppet valve assemblies to service the shared combustion chamber, while eliminating the need for a separate cylinder head to house the valve assemblies, thereby minimizing the size, weight and vertical profile of the engine for equivalent power requirements and providing for smoother, more efficient and less polluting operation.	3.640625	4	[ -0.009033203125, 0.0028533935546875, 0.0191650390625, -0.01177978515625, -0.009521484375, -0.00157928466796875, 0.006317138671875, -0.00051116943359375, -0.00958251953125, -0.00726318359375, 0.0106201171875, -0.00628662109375, -0.028076171875, -0.009521484375, -0.0010833740234375, -0.0050048828125, -0.009033203125, -0.00018215179443359375, 0.008056640625, -0.00811767578125, 0.047607421875, 0.007354736328125, -0.014404296875, 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1.. Introduction {#s1} ================ Carbon nanotubes (CNTs) were discovered by Sumio Iijima in 1991 \[[@C1]\] and since then, they have received high attention due to their extraordinary mechanical, electrical and thermal properties. Besides that, CNTs have very low density \[[@C2]\] and very high aspect ratio. CNTs consist of graphene sheets coaxially rolled into hollow cylinders, and can be single-walled or multi-walled depending on the number of graphene sheets. Moreover, CNTs can be metallic or semiconducting depending on the twist of the tubes. In contrast to CNTs, carbon nanofibers (CNFs) comprise cone-shaped graphene layers stacked on top of each other creating completely filled cylinders, which also have excellent mechanical, thermal and electrical properties. At 400 and 7 GPa, the Young modulus and tensile strength of CNFs are higher than those of steel \[[@C3]\]. The thermal conductivity of CNFs (about 1900 W mK^−1^) is five times higher than copper \[[@C4]\] and can carry current density of about 12 MA cm^−2^ which is three times higher than copper \[[@C5], [@C6]\]. CNFs exhibit many significant advantages over CNTs, since they can be grown at lower temperatures and they are 100% metallic, whereas 2/3 of CNTs are semiconducting when grown in bulk \[[@C7]\]. Because of these excellent properties CNFs have potential applications in electrical interconnects \[[@C8]\], as thermal interface materials, as reinforcement additives in polymer composites and as electrodes for supercapacitors. The carbon nanostructures, including CNFs, can be synthesized in several ways including electrospinning, chemical vapor deposition (CVD), laser ablation and arc discharge. There are different types of CVD and these are classified on the basis of energy type used during deposition: microwave plasma enhanced CVD, thermal CVD and direct current plasma enhanced CVD (DC-PECVD) \[[@C9]--[@C11]\]. Depending on the catalyst and the CVD growth method used, different types of carbon nanostructures are obtained. The DC-PECVD method has an advantage over the other growth methods in that it provides high purity and vertical alignment of the produced CNFs \[[@C12]\]. To grow CNFs using CVD, the deposition of catalytic particles on a substrate is required. Transition metals such as iron, cobalt, palladium and nickel are often used as catalysts \[[@C11], [@C13]--[@C15]\]. The catalysts can be deposited in different ways onto the substrate such as deposition of a pure metal film using sputtering or e-beam evaporation techniques and deposition of a nanoparticle (NP)-containing solution via spin coating, dip-coating or spraying methods \[[@C16]--[@C18]\]. The physical vapor deposition (PVD) deposition methods, such as sputtering or evaporation, require expensive equipment, a metal target, clean room laboratory facilities and costly equipment maintenance. In the present study, catalytic palladium NPs are deposited on silicon substrate via spin-coating using highly stable and inexpensive polymer--Pd colloidal solutions. CNFs are then grown on these catalyst particles at complementary metal oxide semiconductor (CMOS) process-compatible temperature thus allowing CNFs to be used in on-chip thermal, electrical and energy storage solutions. Two types of polymer--Pd NPs solutions were used to deposit the palladium catalyst particles: (1) poly(vinylpyrro1idone)-Pd (PVP--Pd) NPs stabilized in methanol solution and (2) poly(lauryl methacrylate)-block-poly(2-(acetoacetoxy)ethyl methacrylate) (LauMA~x~-b-AEMA~y~/Pd) micellar nanohybrids stabilized in n-hexane. Different types of polymers are used due to their different thermal stabilization temperatures. The polymers are stable up to certain temperature and burn off when heated to higher temperature thus leaving Pd NPs on the surface of the substrate. The stabilization temperature of LauMA~x~-b-AEMA~y~ and PVP polymers is around 200 °C and 400 °C respectively \[[@C19]\]. The synthesis and characterization of the aforementioned polymer-stabilized Pd NPs has been reported in other studies \[[@C20]--[@C23]\]; however, in this work these polymer-metal nanohybrids have been employed for the growth of CNFs. The use of such catalyst-containing solutions is advantageous since those are nontoxic, cheap and can be easily prepared using low-cost wet-chemistry procedures. In addition, their deposition onto selected substrates does not require the use of expensive equipment. Moreover, the polymers can be easily washed away and the substrate can be reused in case of process failure during NPs deposition. This is a rapid and industry compatible deposition method that can be used to grow a film of CNFs at the backside of a chip for heat sink applications. Three different PVP--Pd nanohybrid solutions were prepared in methanol, in which the polymer content was kept constant and only the palladium content varied. In the case of the LauMA~x~-b-AEMA~y~/Pd micellar systems stabilized in n-hexane, two different block copolymers (polymer A: x = 120, y = 67; polymer B: x = 50, y = 9) are employed as the palladium NPs stabilizing agents. The CNFs were grown using the DC-PECVD technique at different temperatures i.e. at a high temperature (550 °C), at a CMOS compatible temperature (390 °C) and even at 40 °C lower (350 °C). The specific capacitance and cyclability of the CNFs were measured using cyclic voltammetry to demonstrate the electrical properties and applicability of these nanostructures as supercapacitor electrodes directly built on CMOS chips. 2.. Fabrication, characterization and measurements {#s2} ================================================== The synthetic methodologies followed for the preparation of the PVP--Pd and the LauMA~x~-b-AEMA~y~-Pd hybrid solutions are described below.(1)A typical synthetic methodology followed for the synthesis of the PVP--Pd nanohybrid colloidal systems (moles vinyl pyridine units/moles palladium salt = 9:1) is described as follows \[[@C19], [@C23]\]: in a round bottom flask equipped with a magnetic stirrer, PVP (1 g, 9 × 10^−3^ moles of vinylpyrridine units) (Sigma-Aldrich, MW = 1300 000) was dissolved in methanol (10 mL). Subsequently, palladium acetate (0.22 g, 1 × 10^−3^ moles) (Pd(OAc)~2~, Sigma-Aldrich, 98%) was added to the polymer solution and the reaction flask was placed under reflux for 2 h. During this period, the color of the solution changed from yellow to dark brown indicating the formation of palladium NPs. After the completion of the reaction, the brown-colored solution was left to cool down to room temperature and it was then stored in sealed glass vials. The solutions were highly stable and no precipitation was observed even after several months.The above-mentioned methodology was employed for synthesizing two more PVP--Pd nanohybrid colloidal systems stabilized in methanol, in which the polymer content was kept the same and only the metallic (Pd) content varied i.e. the molar ratio of the vinyl pyridine units to the palladium salt was 18:1 and 38:1.(2)The Pd-containing LauMA~x~-b-AEMA~y~ micellar hybrids have been prepared in n-hexane by following a previously reported methodology \[[@C20], [@C22]\]. Exemplarily, the procedure followed for the synthesis of the LauMA~120~-b-AEMA~67~/Pd micellar nanohybrids is described as follows: LauMA~120~-b-AEMA~67~ (20 mg, 0.03 mmoles of AEMA units) was dissolved in n-hexane (5 mL). After complete dissolution of the polymer, triethylamine (0.021 mL, 0.15 mmoles ) was added. Subsequently, the polymer solution was transferred into a glass vial containing Pd(OAc)~2~ (3.40 mg, 0.015 mmoles) and the mixture was left to stir at room temperature until complete solubilization of the salt. Upon complexation and solubilization, the color of the solution changed from white to yellow transparent. Finally, the reducing agent namely hydrazine monohydrate (1.46 μL, 0.03 mmoles) was added to the solution upon stirring. This was accompanied by a color change of the solution from yellow to dark brown indicating the reduction of palladium (II) ions into metallic palladium (0) NPs. The resulting solution was left to stir for 24 h at room temperature. The size of the palladium NPs generated within the micellar cores has been already reported \[[@C22]\]. The average diameter of the palladium NPs is 2.3 ± 0.3 nm for the LauMA~50~-b-AEMA~9~/Pd(solution A) and 8.8 ± 1.7 nm for LauMA~120~-b-AEMA~67~/Pd(solution B). A 2 inch n-type silicon wafer was used as a substrate for the uniform deposition of the polymer-palladium solutions. Titanium/titanium nitride (Ti/TiN) of thicknesses 50 and 100 nm were sputtered on each side of the chip using FHR MS 150 sputter machine in order to have better electrical contact between back and front side of the sample, because of backside probing of the chip for measurements. The polymer-palladium NPs solutions were later spun using standard resist spinners. Vertically aligned CNFs were grown at different temperatures by the DC-PECVD method as described in \[[@C8], [@C24]\]. A mixture of acetylene and ammonia gases was used where the acetylene is the source gas and the ammonia is a carrier gas. The growth was executed for 2 h on all samples. The temperature of the heater is measured and regulated during the whole growth process to an accuracy of ±2° using a built-in thermocouple inside the grounded heating plate. The chips were weighed before the deposition of the palladium NPs and after the growth of CNFs for determining the weight of the CNFs including catalyst, a parameter used in evaluating the capacitance per gram of such electrodes. The weight measurements were performed using a high precision balance 'Sartorius Analytical Balance BP211D' with a resolution of 10 μg. Transmission electron microscopy (TEM) analysis performed on the LauMA~x~-b-AEMA~y~/Pd (solution A) system was carried out on a 1010 JEOL microscope (200 kV). The suspension of MNPs was dried on a carbon coated copper grid to allow the TEM investigation. The scanning electron microscopy (SEM) analysis of the CNFs was conducted using JEOL JSM-6301F. In order to see the morphology of the CNFs, images were taken at 40° tilt angle as well as top view images at zero tilt. Cyclic voltammetry (CV) was performed to evaluate the capacitance. A three electrode setup was used with a silver/silver chloride (Ag/AgCl) electrode as the reference electrode and platinum mesh as the counter electrode. The electrolyte used was 1M KOH (99.99%, Aldrich). The limit of measuring the electrode cell was one centimeter diameter disk. The samples were mounted and dipped in the electrolyte solution for a few minutes while nitrogen gas was blowing to wet the CNFs. The CV curve was obtained using Gamry Instruments Reference 600 (Framework 6.1). The voltage sweep ranging from −0.2 to 0.3 V was applied and different voltage scan rates were used. The voltammetry using 10 mV s^−1^ scan rate was carried out for 18 cycles to exclude the doubt of initial surface reactions whereas 5 cycles were run for other scan rates. The same measurement was also performed for 1000 cycles to measure the cyclability at 20 mV s^−1^ scan rate while keeping the other parameters the same. The ideal double layer capacitance behavior is the rectangular shape of the voltammetry characteristics drawn between current and voltage \[[@C25]\]. 3.. Results and discussion {#s3} ========================== Information on the palladium NPs content (provided as the molar ratio of the metal-binding units of the polymer to the palladium salt precursor), growth temperature, weight of CNFs and capacitance is provided in table [1](#TB1){ref-type="table"}, whereas the specific capacitance measured at different voltage scan rates is given in table [2](#TB2){ref-type="table"}. ###### Properties of the CNFs grown using different polymer-palladium NPs solutions at different temperatures, their capacitance and specific capacitance mF cm^−2^ (per footprint area). \[vinyl pyridine\]/\[Pd(OAc)~2~\] Growth temperature (°C) Weight (μg) Length (μm) Capacitance (mF) Specific capacitance (mF cm^−2^) ----------------------------------- ------------------------- --------------- --------------- ------------------ ---------------------------------- Bare chip 0.1 0.12 38:1 550 53 14 0.8 1 18:1 550 245 9 3.1 4 9:1 550 916 5 7.1 9 9:1 390 612 1 2.6 3.3 \[AEMA\]/\[Pd(OAc)~2~\] \[LauMA~120~-b-AEMA~67~\] 2:1 390 654 1 2.1 2.7 \[LauMA~50~-b-AEMA~9~\] 2:1 390 115 2 1.4 1.8 \[LauMA~120~-b-AEMA~67~\] 2:1 350 250 1.4 3.1 4 \[LauMA~50~-b-AEMA~9~\] 2:1 350 115 1.6 0.2 0.2 ###### Specific capacitance mF cm^−2^ (per footprint area) measured at different voltage scan rates. \[vinyl pyridine\]/\[Pd(OAc)~2~\] T (°C) 10 mV s^−1^ 20 mV s^−1^ 50 mV s^−1^ 100 mV s^−1^ ----------------------------------- ---------- ------------- ------------- ------------- -------------- PVP/Pd 38:1 550 1 0.8 0.7 0.6 PVP:Pd 18:1 550 4 2.4 1.6 1.2 PVP/Pd 9:1 550 9\. 6 4.6 4 PVP/Pd 9:1 390 3.3 2.6 2 2 \[AEMA\]/\[Pd(OAc)~2~\] Solution A 350 0.2 0.2 0.15 0.14 Solution B 390 2.7 2 1.5 1.3 Solution B 350 4 3 2.3 2 Solution A 390 1.8 1.41 1.1 1 A representative TEM image of the solution A system is provided in figure [1](#F1){ref-type="fig"}. As seen in the image, tiny, spherical palladium NPs can be visualized with average diameters in the range 2.3 ± 0.3 nm. The presence of a few larger aggregates may be due to drying-induced aggregation during TEM sample preparation. In the case of the PVP/Pd systems, HRTEM analysis revealed that the palladium NPs are nanocrystals with average diameters below 10 nm. The crystalline planes (111) and (200) of palladium NP could be visualized with characteristic interplanar distances of 2.27 and 1.97 Å, respectively \[[@C26]\]. Tilted view and top view (inset on each picture) SEM images of CNFs grown at 550 °C using three PVP/Pd solutions having different metallic (palladium) content are shown in figures [2](#F2){ref-type="fig"}(a)--(c) whereas SEM images of the CNFs grown at 390 °C using the PVP/Pd (1:9) solution is provided in figure [2](#F2){ref-type="fig"}(d). ![TEM image of the LauMA~50~-b-AEMA~9~/Pd system (solution A).](TSTA1166125201){#F1} ![SEM images of CNFs grown by DC-PECVD for 2 h at different temperatures on palladium NPs using various PVP--Pd colloidal solutions given as (a) PVP:Pd 38:1, growth at 550 °C. (b) PVP:Pd 18:1, growth at 550 °C. (c) PVP:Pd 9:1, growth at 550 °C. (d) PVP:Pd 9:1, growth at 390 °C.](TSTA1166125202){#F2} Similarly, the tilted view and top view (inset on each picture) SEM images of the CNFs grown at 390 and 350 °C using solution A and solution B are shown in figures [3](#F3){ref-type="fig"}(b), (d) and (a), (c). ![SEM images of CNFs grown by DC-PECVD for 2 h on two different LauMA~x~-b-AEMA~y~/Pd micellar solutions at different temperatures given as (a) LauMA~120~-b-AEMA~67~/Pd (solution B) growth at 390 °C. (b) LauMA~50~-b-AEMA~9~/Pd (solution A) growth at 390 °C. (c) LauMA~120~-b-AEMA~67~/Pd (solution B) growth at 350 °C. (d) LauMA~50~-b-AEMA~9~/Pd (solution A) growth at 350 °C.](TSTA1166125203){#F3} It is clear from the SEM images that the CNFs grown at lower temperature 350 °C are vertically aligned similar to those grown at the highest temperature (550 °C) as shown in figures [2](#F2){ref-type="fig"} and [3](#F3){ref-type="fig"}. In addition, inset of figures [2](#F2){ref-type="fig"} and [3](#F3){ref-type="fig"} also show the uniform growth of CNFs confirming the uniform deposition of palladium catalyst NPs using spin-coating, which is in line with \[[@C26]\]. Moreover, in the case of the PVP--Pd systems, the CNF density increases significantly by increasing the palladium content within the PVP--Pd colloidal hybrid solutions i.e. from 38:1 to 18:1 and to 9:1 (figures [2](#F2){ref-type="fig"}(a)--(c) respectively) thus resulting in an increase in CNF weight, as shown in table [1](#TB1){ref-type="table"}. In addition, SEM analysis also reveals that under identical growth conditions, the CNFs grown using the highest palladium-containing system (9:1) are shorter in length compared to those grown using the lowest palladium-containing system (38:1). By using the same palladium-containing system (9:1) the CNFs grown at higher (550 °C) temperatures are much longer than those grown at 390 °C, in line with the weight measurements, although less dense than the CNFs grown at 390 °C. In the case of the LauMA~x~-b-AEMA~y~/Pd solutions, the average diameter of the palladium nanocatalyst is 2.3 ± 0.3 nm for solution A and 8.8 ± 1.7 nm for solution B. Despite their size differences both systems are found within the optimum size range enabling CNF growth at a low temperature (350 °C) as seen in the SEM images provided in figures [3](#F3){ref-type="fig"}(c) and (d). The top view SEM images (inset in figure [3](#F3){ref-type="fig"}) clearly show that under identical growth temperature, the CNFs grown using solution B are denser and heavier than those grown using solution A, but shorter in length compared to those obtained from solution A, as shown in table [1](#TB1){ref-type="table"}. Furthermore, when the growth is performed at different temperatures, solution B gives longer but less dense CNFs at low temperature 350 °C. On the other hand, solution A gives denser and shorter CNFs at the same growth temperature. The CV curves for the electrical characterization of the CNFs grown using the PVP--Pd and the LauMA~x~-b-AEMA~y~-Pd solutions are provided in figures [4](#F4){ref-type="fig"}(a), (b) and [5](#F5){ref-type="fig"}(a). The specific capacitance (mF cm^−2^ footprint area) curves measured at difference voltage scan rate are shown in figures [4](#F4){ref-type="fig"}(c) and [5](#F5){ref-type="fig"}(b). The cyclability curves for 1000 cycles are shown in figures [4](#F4){ref-type="fig"}(d) and [5](#F5){ref-type="fig"}(c) whereas magnified images of the last 20 cycles from 980 to 999 are shown in figures [4](#F4){ref-type="fig"}(e) and [5](#F5){ref-type="fig"}(d). ![Cyclic voltammetry curves of CNFs. (a) At 550 °C using different PVP--Pd solutions with different palladium content. (b) At 550 °C and 390 °C using PVP:Pd 9:1solution. (c) Specific capacitance (mF cm^−2^ foot print area) versus voltage scan rate. (d) Cyclability of CNFs grown at 550 °C and 390 °C using PVP:Pd 9:1 solution (normalized by specific capacitance of first cycle). (e) Cycles from 975 to 999.](TSTA1166125204){#F4} ![(a) Cyclic voltammetry curves of CNFs grown using solution A and solution B at 350 °C and 390 °C. (b) Specific capacitance (mF cm^−2^ foot print area) versus voltage scan rate. (c) Cycle life of solution B (normalized by specific capacitance of first cycle). (d) Cycles from 980 to 999.](TSTA1166125205){#F5} The voltammograms given in figures [4](#F4){ref-type="fig"}(a), (b) and [5](#F5){ref-type="fig"}(a) are fairly rectangular showing the double layer capacitive behavior of the CNFs obtained using both types of polymer--Pd catalyst solutions, however, the peaks at extreme sweep voltages show some pseudocapacitive charge storage which may arise from the reaction of underlayer with aqueous electrolyte. At 550 °C growth temperature and 10 mV s^−1^ scan rate, the specific capacitance (per cm^−2^ foot print area) is larger (9 mF cm^−2^) for higher concentration (9:1) of palladium NPs in the PVP--Pd solution and lower (1 mF cm^−2^) for lower concentration (38:1) confirming the active capacitive role of CNFs. In fact, shorter but denser CNFs for the (9:1) solution give a higher surface area accessible to electrolyte than longer but less dense CNFs for the (38:1) solution, and the higher surface area results in higher current on voltammogram and hence higher specific capacitance as shown in figure [4](#F4){ref-type="fig"}(a) and table [1](#TB1){ref-type="table"}. In addition the specific capacitance is 3.3 mF cm^−2^ for the CNFs grown at 390 °C using the PVP--Pd (9:1) solution. In the case of the LauMA~x~-b-AEMA~y~/Pd solutions the specific capacitance is higher (2.7 and 4 mF cm^−2^) for CNFs synthesized using solution B than solution A when grown at corresponding temperatures 350 °C and 390 °C which is in line with the weight of the CNFs. Moreover, for the same solution, the longer CNFs give a higher surface area which results in higher current on the voltammogram and hence higher specific capacitance, as shown in figure [5](#F5){ref-type="fig"}(a) and table [1](#TB1){ref-type="table"}. The capacitive behavior indicates the similar electrical behavior of CNFs grown at both low and high temperatures. The specific capacitance at 100 mV s^−1^ ranges from 3.9 to 0.140 mF cm^−2^. This specific capacitance is many folds higher than the recently reported capacitance obtained from the CVD grown vertically aligned CNFs \[[@C27]\]. Furthermore, the maximum specific capacitance at 100 mV s^−1^ scan rate is 3.9 mF cm^−2^ obtained from the CNFs grown at 550 °C, table [2](#TB2){ref-type="table"}, which is almost equal to the maximum reported capacitance obtained from graphene-CNT based microcapacitors (3.93 mF cm^−2^) synthesized on a similar silicon substrate but using a longer voltage scan range \[[@C28]\]. Moreover, the specific capacitance obtained from CNFs grown at low temperature 350 °C and 390 °C, table [2](#TB2){ref-type="table"}, is 1.9--2 mF cm^−2^, half of the reported specific capacitance mentioned above, nevertheless the growth temperature of CNFs here is below the CMOS process-compatible temperature. In addition, the cyclic voltammetry at different voltage scan rates shows that specific capacitance decreases by increasing the scan rate from 10 to 100 mV s^−1^ for both polymer--Pd types used, figures [4](#F4){ref-type="fig"}(c) and [5](#F5){ref-type="fig"}(b), due to a kinetically slow faradaic reaction on the electrode surface which does not take place at high scan rate[^5^](#stam508704fn1){ref-type="fn"} [^1]. Moreover, the cycle life curves of both polymer--Pd solution types show the decrease in specific capacitance with increase in cycles, figures [4](#F4){ref-type="fig"}(d) and [5](#F5){ref-type="fig"}(c), which eventually becomes uniform and remains unchanged as shown in the plots of the last 20 cycles, given in figures [4](#F4){ref-type="fig"}(e) and [5](#F5){ref-type="fig"}(d). The more than 90% capacitance retention for CNFs grown from the PVP--Pd solution and 80% for the CNFs grown from solution B after 1000 cycles of cyclic voltammetry proves the long cycle life of these materials as supercapacitor electrodes. Due to the lower density of CNFs for solution B the electrolyte damages the metal underlayer in between the CNFs thus resulting in lower capacitance after 1000 cycles. The above results indicate that the CNFs grown from all types of polymer-stabilized Pd nanocatalysts are vertically aligned similar to CNFs grown from a PVD deposited catalyst film. Moreover the density and weight of the CNFs grown from a PVP--Pd solution can be controlled by controlling the palladium contents in the PVP--Pd solution in the tested concentration range. Furthermore CNFs of different diameters can be grown from LauMA~x~-b-AEMA~y~/Pd solutions. Finally, the electrical characterization proves that electrical properties of all the CNFs are the same; however, the low capacitance in solution A is due to the lower density of CNFs in the footprint area. The CNF growth performed at this temperature has created the opportunity to grow the CNFs directly on CMOS chips. The possibility of CNF growth at temperatures lower (350 °C) than CMOS temperature ensures their usage even if the CMOS temperature drops further. 4.. Conclusions {#s4} =============== Catalytic palladium NPs of various sizes were deposited on a silicon substrate via spin-coating using two types of highly stable and cost-effective polymer--Pd colloidal solutions. More precisely, PVP or methacrylate-based diblock copolymers of the type LauMA~x~-b-AEMA~y~ were employed as steric stabilizers for palladium NPs in organic solvents. Vertically aligned CNFs were synthesized on these palladium nanocatalysts using the direct plasma enhanced CVD technique at different temperatures ranging from 550 °C down to 350 °C, which can be considered as a CMOS-compatible temperature. The SEM characterization had shown that the CNFs grown at low temperature were vertically aligned similar to those generated at high temperature. The capacitive behavior and long cyclability had proven not only the suitability of the as-grown CNFs as electrodes for supercapacitors but also that the CNFs grown at low and high temperatures had similar electrical behavior. We have demonstrated a CMOS compatible process to build efficient heat sink, interconnects or supercapacitor electrodes directly on the chip based on vertically aligned CNFs as the active material. This work has been performed within the MNT-ERA.NET Carpolcap project supported by Vinnova, the Swedish Governmental Agency for Innovation Systems and the Cyprus Research Promotion Foundation (Grant No. KOINA/MNT-ERA.NET/0311/01). The authors thank Dr Rodica Paula Turcu (National Institute for Isotopic and Molecular Technologies, Cluj-Napoca, Romania) for performing the TEM characterization on the LauMA~50~-b-AEMA~9~/Pd system and Dr Maria Demetriou for the synthesis of the LauMA-b-AEMA block copolymers used in the present study. [^1]: [www.gamry.com/application-notes/testing-electrochemical-capacitors-part-1-cyclic-voltammetry-and-leakage-current/](http://www.gamry.com/application-notes/testing-electrochemical-capacitors-part-1-cyclic-voltammetry-and-leakage-current/), accessed successfully on 06-10-2014.	3.265625	3	[ -0.009765625, -0.0068359375, 0.0045166015625, 0.006744384765625, 0.0152587890625, -0.006439208984375, 0.00164031982421875, -0.005035400390625, 0.0106201171875, 0.021240234375, -0.00119781494140625, 0.0101318359375, -0.003814697265625, -0.0084228515625, 0.00994873046875, -0.00147247314453125, -0.00848388671875, 0.006072998046875, -0.012451171875, -0.016845703125, -0.00018978118896484375, 0.007537841796875, 0.0078125, 0.00390625, -0.00836181640625, -0.0006103515625, 0.00213623046875, 0.014404296875, 0.00555419921875, 0.0079345703125, 0.0146484375, -0.00060272216796875, 0.005157470703125, 0.000579833984375, -0.0145263671875, 0.012451171875, -0.01275634765625, -0.0089111328125, -0.0048828125, 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eso1544 — Science Release The Glowing Halo of a Zombie Star VLT maps out remains of white dwarf’s meal The remains of a fatal interaction between a dead star and its asteroid supper have been studied in detail for the first time by an international team of astronomers using the Very Large Telescope at ESO’s Paranal Observatory in Chile. This gives a glimpse of the far-future fate of the Solar System. Led by Christopher Manser, a PhD student at the University of Warwick in the United Kingdom, the team used data from ESO’s Very Large Telescope (VLT) and other observatories to study the shattered remains of an asteroid around a stellar remnant — a white dwarf called SDSS J1228+1040 [1]. Using several instruments, including the Ultraviolet and Visual Echelle Spectrograph (UVES) and X-shooter, both attached to the VLT, the team obtained detailed observations of the light coming from the white dwarf and its surrounding material over an unprecedented period of twelve years between 2003 and 2015. Observations over periods of years were needed to probe the system from multiple viewpoints [2]. “The image we get from the processed data shows us that these systems are truly disc-like, and reveals many structures that we cannot detect in a single snapshot,” explained lead author Christopher Manser. The team used a technique called Doppler tomography — similar in principle to medical tomographic scans of the human body — which allowed them to map out in detail the structure of the glowing gaseous remains of the dead star’s meal orbiting J1228+1040 for the first time. While large stars — those more massive than around ten times the mass of the Sun — suffer a spectacularly violent climax as a supernova explosion at the ends of their lives, smaller stars are spared such dramatic fates. When stars like the Sun come to the ends of their lives they exhaust their fuel, expand as red giants and later expel their outer layers into space. The hot and very dense core of the former star — a white dwarf — is all that remains. But would the planets, asteroids and other bodies in such a system survive this trial by fire? What would be left? The new observations help to answer these questions. It is rare for white dwarfs to be surrounded by orbiting discs of gaseous material — only seven have ever been found. The team concluded that an asteroid had strayed dangerously close to the dead star and been ripped apart by the immense tidal forces it experienced to form the disc of material that is now visible. The orbiting disc was formed in similar ways to the photogenic rings seen around planets closer to home, such as Saturn. However, while J1228+1040 is more than seven times smaller in diameter than the ringed planet, it has a mass over 2500 times greater. The team learned that the distance between the white dwarf and its disc is also quite different — Saturn and its rings could comfortably sit in the gap between them [3]. The new long-term study with the VLT has now allowed the team to watch the disc precess under the influence of the very strong gravitational field of the white dwarf. They also find that the disc is somewhat lopsided and has not yet become circular. “When we discovered this debris disc orbiting the white dwarf back in 2006, we could not have imagined the exquisite details that are now visible in this image, constructed from twelve years of data — it was definitely worth the wait,” added Boris Gänsicke, a co-author of the study. Remnants such as J1228+1040 can provide key clues to understanding the environments that exist as stars reach the ends of their lives. This can help astronomers to understand the processes that occur in exoplanetary systems and even forecast the fate of the Solar System when the Sun meets its demise in about seven billion years. Notes [1] The white dwarf’s full designation is SDSS J122859.93+104032.9. [2] The team identified the unmistakable trident-like spectral signature from ionised calcium, called the calcium (Ca II) triplet. The difference between the observed and known wavelengths of these three lines can determine the velocity of the gas with considerable precision. [3] Although the disc around this white dwarf is much bigger than Saturn’s ring system in the Solar System, it is tiny compared to the debris discs that form planets around young stars. More information This research was presented in a paper entitled “Doppler-imaging of the planetary debris disc at the white dwarf SDSS J122859.93+104032.9”, by C. Manser et al., to appear in the Monthly Notices of the Royal Astronomical Society. The team is composed of Christopher Manser (University of Warwick, UK), Boris Gaensicke (University of Warwick), Tom Marsh (University of Warwick), Dimitri Veras (University of Warwick, UK), Detlev Koester (University of Kiel, Germany), Elmé Breedt (University of Warwick), Anna Pala (University of Warwick), Steven Parsons (Universidad de Valparaiso, Chile) and John Southworth (Keele University, UK). ESO is the foremost intergovernmental astronomy organisation in Europe and the world’s most productive ground-based astronomical observatory by far. It is supported by 16 countries: Austria, Belgium, Brazil, the Czech Republic, Denmark, France, Finland, Germany, Italy, the Netherlands, Poland, Portugal, Spain, Sweden, Switzerland and the United Kingdom, along with the host state of Chile. ESO carries out an ambitious programme focused on the design, construction and operation of powerful ground-based observing facilities enabling astronomers to make important scientific discoveries. ESO also plays a leading role in promoting and organising cooperation in astronomical research. ESO operates three unique world-class observing sites in Chile: La Silla, Paranal and Chajnantor. At Paranal, ESO operates the Very Large Telescope, the world’s most advanced visible-light astronomical observatory and two survey telescopes. VISTA works in the infrared and is the world’s largest survey telescope and the VLT Survey Telescope is the largest telescope designed to exclusively survey the skies in visible light. ESO is a major partner in ALMA, the largest astronomical project in existence. And on Cerro Armazones, close to Paranal, ESO is building the 39-metre European Extremely Large Telescope, the E-ELT, which will become “the world’s biggest eye on the sky”. Links Contacts Christopher Manser University of Warwick United Kingdom Email: C.Manser@warwick.ac.uk Boris Gänsicke University of Warwick United Kingdom Tel: +44 (0)2476574741 Email: Boris.Gaensicke@warwick.ac.uk Tom Frew International Press Officer, University of Warwick United Kingdom Tel: +44 (0)24 7657 5910 Cell: +44 (0)7785 433 155 Email: a.t.frew@warwick.ac.uk Richard Hook ESO Public Information Officer Garching bei München, Germany Tel: +49 89 3200 6655 Cell: +49 151 1537 3591 Email: rhook@eso.org Connect with ESO on social media	3.328125	3	[ 0.0004749298095703125, -0.005706787109375, -0.0111083984375, -0.0218505859375, -0.01080322265625, -0.01129150390625, -0.0277099609375, 0.0025787353515625, 0.002655029296875, -0.021240234375, -0.0036163330078125, 0.0191650390625, -0.040771484375, 0.0196533203125, -0.002777099609375, -0.001983642578125, -0.0169677734375, 0.01116943359375, 0.0035552978515625, -0.004364013671875, -0.0128173828125, -0.01531982421875, -0.0042724609375, 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Quantum teleportation provides a means to transport an unknown quantum state from one location to another over arbitrary distances. Since originally being proposed in 1993[@b1], the study on quantum teleportation has aroused great interest. Its experimental realizations in various different ways have been reported. For instance, the best known methods have been implemented using photon polarization and optical techniques[@b2][@b3], by means of squeezed states of light[@b4], by applying nuclear magnetic resonance (NMR) techniques[@b5], and by a hybrid technique[@b6][@b7]. Teleportation has also been accomplished between photons and a single atomic ensemble[@b8][@b9], between distant atomic objects[@b10][@b11][@b12][@b13], and in a chip-based superconducting circuit architecture[@b14]. Quantum teleportation is essential for large-scale quantum communication[@b15][@b16][@b17] and distributed quantum networks[@b18]. It has proven to be a useful tool for realizing universal quantum logic gates in quantum computing and general quantum information manipulation[@b19]. However, all protocols for accomplishing quantum teleportation require non-local correlations, or Einstein--Podolsky--Rosen (EPR) entanglement, between systems shared by the sender and receiver. On the other hand, non-separable correlations among two or more different degrees of freedom from the same classical optical beam, have been discussed[@b20][@b21][@b22][@b23][@b24][@b25][@b26][@b27][@b28][@b29][@b30][@b31][@b32]. The violation of Bell\'s inequality or GHZ theorem for such a non-separable correlation has been demonstrated experimentally[@b20][@b21][@b22][@b23][@b24][@b25]. Thus, a non-separable classical correlation is called "nonquantum entanglement" or "classical entanglement"[@b25][@b26][@b27][@b28][@b29][@b30]. Such a classical entanglement has been applied to resolve basic issues in polarization optics[@b25], simulate quantum walks, et al.[@b27]. The investigations have shown that quantum optical procedures requiring entanglement without non-locality can actually be achieved in classical optics regime[@b25][@b26][@b27][@b28][@b29][@b30][@b31][@b32]. Recently, some discussions on the non-local classical optical correlation of two coherent light beams have been done[@b33][@b34][@b35][@b36]. Some studies, which have attempted to simulate the quantum teleportation by classical optics, have been performed[@b29][@b30][@b31]. However, the classical correspondence on the true meaning of quantum teleportation, which is based on the classical EPR correlation state, has not been achieved. In this work, we present a new method to construct a non-local classical EPR correlation state by using two incoherent light beams and implement a classical analogy on the true meaning of quantum teleportation. Results and Discussion ====================== Non-local classical optical correlation --------------------------------------- Initially two independent light beams, E~1~ and E~2~ with different wavelengths, are considered and pass through a 50/50 beam splitter (BS) as shown in [Fig. 1](#f1){ref-type="fig"}. The fields of two light beams satisfy complete incoherent condition and . Here and t represent coordinates of space and time. After the BS and a half-wave plate (HWP) in one output of the BS, two new outputs with and can be obtained, where and refer to the horizontal and vertical polarization components, respectively. In order to analyze the correlation properties between and , a half-wave plate (HWP) and a polarizing beam splitter (PBS) are introduced in each path. They function to rotate angles of the light beam and separate and polarized light. Here θ~a~ and θ~b~ represent polarization rotated angles in two paths, respectively. After the HWP and PBS, two polarized beams become four beams. Their fields are described by E~ah~, E~av~, E~bh~ and E~bv~, respectively, which can be modulated by θ~a~ and θ~b~. Now we perform the famous Clauser--Horne--Shimony--Holt (CHSH) test in our system as shown in [Fig. 1](#f1){ref-type="fig"}. The correlation function is defined in the following form[@b20]:where P~HH~ = N~HH~ (θ~a~,θ~b~)/N~Total~, P~VV~ = N~VV~ (θ~a~,θ~b~)/N~Total~, P~HV~ = N~HV~ (θ~a~,θ~b~)/N~Total~, and P~VH~ = N~VH~ (θ~a~,θ~b~)/N~Total~ are normalized correlated probabilities when polarizations of each beam are measured, and N~Total~ = N~HH~ (θ~a~,θ~b~) + N~VV~ (θ~a~,θ~b~) + N~HV~ (θ~a~,θ~b~) + N~VH~ (θ~a~,θ~b~). In our experiment, such correlated probabilities can be represented by the first order correlation of electric fields through N~IJ~ (θ~a~,θ~b~) (I(J) represents H or V):In the experiment the fields of output lights are not directly measured. However, the first-order field correlation can be obtained through measuring the difference of light intensities at two export positions on Mach-Zehnder interferometer, because . Here I~1~ and I~2~ represent the light intensities at two export positions of the Mach-Zehnder interferometer and ΔI is the difference between them. More information about the measurement method for the first-order field correlation is provided in the Methods section. [Figure 2](#f2){ref-type="fig"} shows experimental results for the correlation functions C(θ~a~,θ~b~) as a function of polarization rotated angle θ~a~ at some certain θ~b~. Here two laser beams (continuous wave mode) with different wavelengths, 532 nm and 632.8 nm, are used. Their intensities are taken as 2 mW. The circle dots and solid lines represent the experimental measurements and theoretical results, respectively. It can be seen that the experimental results are in good agreement with the theoretical calculations. After we have obtained C(θ~a~,θ~b~), the CHSH formulation of Bell\'s measurement is used to quantify such correlation. The CHSH measurement isIt is well known that the local realism theories give \\|B\\| \< 2. However, from the experimental results marked by dashed lines in [Fig. 2](#f2){ref-type="fig"}, B = 2.597 ± 0.012 \> 2 is obtained as θ~a~ = π/4, θ~b~ = 0, and . The presented experiment yields the strongest violation of Bell\'s inequalities. Any of the four EPR-Bell states can be constructed by adjusting polarization and phase factor via HWP in the above experimental setup. This is highly similar to the production of polarization-entangled photon pairs from spontaneous down-conversion of nonlinear crystals[@b37]. For example, the output fields and shown in [Fig. 1](#f1){ref-type="fig"} correspond to the following symmetric Bell-state:Here we use the notation \\|h)~i~(\\|v)~i~) to express a classical state[@b29][@b31]. That is to say, if polarization is measured in one beam, the information of polarization can be "determined" in another beam due to the first-order field correlation, and vice versa. This means that a classical correlation state has been constructed. Because the correlation between two beams is independent on the separation between them, such a correlation is non-local and can be regarded as a classical analogy of EPR entangled state in quantum mechanics. The problem is whether or not some unique phenomena such as quantum teleportation can be realized by applying such a classical EPR correlation state, which is similar to the case in quantum information process. Classical analogy of quantum teleportation based on non-local classical correlation ----------------------------------------------------------------------------------- In order to study the classical analogy of quantum teleportation, the experimental setup shown in [Fig. 3](#f3){ref-type="fig"} is considered. The experimental generation of EPR correlation states and Bell-state measurement are two key parts in the teleportation scheme. In this scheme, above classical EPR correlation states are used as the source. A three-photon scheme is referred to for the Bell-state measurement as described by D. Bouwmeester et. al.[@b2]. This system features the antisymmetric state obtained from four Bell-states. Thus, the antisymmetric Bell-state is used in our teleportation scheme: . This corresponds to and in our classical EPR system, which are shared by Alice and Bob, for example. If Alice want to teleport an initial state \\|ψ~c~) = c~1~ \\|h) + c~2~ \\|v) to Bob, she needs perform a joint Bell-state measurement on the initial state and . In the experiments, the field corresponding to the initial state \\|ψ~c~) is expressed as: , where , c~1~ and c~2~ satisfy \\|c~1~\\|^2^ + \\|c~2~\\|^2^ = 1. When c~1~ and c~2~ are considered real, corresponds to the linear polarization case. Whereas, when c~1~ and c~2~ are complex, it is in correspondence to the circular polarization case. We first consider linear polarization case, in which c~1~ and c~2~ can be expressed by the direction angle of polarization θ: c~1~ = cos θ and c~2~ = sin θ. Thus, θ will be the teleported information. In order to perform a joint Bell-state measurement on the initial state and , an optical element group is constructed that includes a BS and two HWPs as shown in [Fig. 3](#f3){ref-type="fig"}. There are two output ports of the BS, in which one is the sum of two input fields, and the other is the difference of the two. Two HWPs are placed at the output port of the difference. The functions of two HWPs are to realize interchange between and polarizations, and add a π phase for the component of polarization field. For such an optical element group, if the input ports are in the Bell-states, it is easy to demonstrate by the correlation measurement of the first-order field that only the output of the antisymmetric state is not zero, and the outputs of three symmetric states all are zero (see Methods section). This is similar to the scheme of the Bell measurements in Ref. [@b2]. Referring back to the previous example, and considering synchronicity of Alice\'s and Bob\' measurements, Alice obtains the information E~ac~ as and enter the optical element group, and then sends it to Bob through the classical channel. Here E~ac~ represents the amplitude of field without any polarization information (see [Supplementary](#s1){ref-type="supplementary-material"}). Owing to lack of technique to measure fields, we had to send the beam to Bob in the experiment. Next, we show that Bob can only use the coherence property of the field rather than the polarization information, and such a process is corresponded to the method used in Ref. [@b2]. After Bob receives the information that Alice sent, he will perform the correlation measurement of the first-order field by using the information and in order to obtain the teleported material. This is because there is a strong correlation between E~ac~ and (see [Supplementary](#s1){ref-type="supplementary-material"}). For example, as passes through a rotated PBS, it will be orthogonally decomposed into E~//~ and as shown in [Fig. 3](#f3){ref-type="fig"}. Our theoretical calculations show that \\|〈E~ac~E~//~〉\\|^2^ = cos^2^ (θ − ϕ) and , which are the correlation of field without polarization (see [Supplementary](#s1){ref-type="supplementary-material"}). Here ϕ represents the rotated angle of the PBS, and is taken as 0° when the polarization of transmission fields is horizontal. From these relations, it is not difficult to find that θ and ϕ are in one-to-one correspondence. If Bob has obtained the maximum of the first-order correlation between E~ac~ and E~//~ for a polarization direction, the corresponding ϕ for such a polarization direction is the teleported information θ (see [Supplementary](#s1){ref-type="supplementary-material"}). In the experiment, the first-order correlations between E~ac~ and E~//~ () are measured by the difference of light intensities, which is similar to the above method for testing CHSH formulation. [Figure 4](#f4){ref-type="fig"} displays the experimental results for the first-order correlation degree, ΔI = I~1~ − I~2~, as a function of the angle ϕ. [Figure 4(a) and (b)](#f4){ref-type="fig"} correspond to the case with θ = 0 for E~//~ and , respectively, whereas the corresponding results for θ = π/4 are plotted in [Fig. 4(c) and (d)](#f4){ref-type="fig"}. From [Fig. 4(a)](#f4){ref-type="fig"}, the maximum of the first-order correlation appears at ϕ = 0, which is in agreement with θ = 0. At the same time, the minimum of the first-order correlation is also found at an orthogonal direction as shown in [Fig. 4(b)](#f4){ref-type="fig"}, which validates realization of the teleportation process. Similarly, as θ = π/4, Bob has measured the maximum of the first-order correlation at ϕ = π/4 and the minimum also appears at its orthogonal direction ([Fig. 4(c) and (d)](#f4){ref-type="fig"}). In fact, the above design is suitable for any linear polarization state. The corresponding experiment to teleport a circular polarized initial state was also performed by using the above scheme, similar teleportation process has been realized (see [Supplementary](#s1){ref-type="supplementary-material"}). In the teleportation process, it is not necessary for Alice to know where Bob is, the initial polarization state can be unknown to anyone not only Alice. Furthermore, the transfer of information from Alice to Bob can happen over arbitrary distances. These properties for the teleportation in the presented scheme completely agree with those described by D. Bouwmeester et. al., which this work\' results focus on[@b2]. Discovery of other schemes for quantum teleportation by using classical optics warrants further study. Conclusions =========== We have demonstrated experimentally the non-local classical optical correlation from the Bell\'s measurement used in tests of quantum non-locality. Based on such a classical EPR correlation, a classical analogy has been implemented to the true meaning of quantum teleportation. The presented results indicate that some non-local phenomena in quantum machines can be realized in classical optical signal processing. Thus, this study opens a new way to obtain the quantum information process in the classical optical communication network. It not only provokes deep thought on some basic physical problems such as essence of entanglement and correlation, but also shows potential application in classical and quantum information processes. Methods ======= Measurement method for the first-order field correlation -------------------------------------------------------- In general, the polarization-entangled photon pairs can be produced from spontaneous down-conversion of the nonlinear crystal. In such a process, the photon states for and polarizations are generated with a certain probability at the same time, which the entangled properties can be measured by the coincidence counts. Based on the coherence of light field, we can construct the corresponding non-local classical EPR correlation states as described by Eq.(4), which the correlated properties can be shown by the first-order field correlation. Basically, the measure of the first-order field correlation can be realized by synchronous local measurements and doesn\'t require direct contact. However, in the experiment it is difficult to obtain the first-order field correlation by directly measuring fields. In addition, the synchronization is very hard to achieve. So, we take the following method, that is, take and for example and do the following Hadamard transformation:thenwhere Re{X} represents the real part of X. From the experimental setup in [Fig.1](#f1){ref-type="fig"}, we can find From complete incoherent condition and ,it is easy to find the following relation:ThenThat is, the first-order field correlation can be measured by the difference of light intensities and this method is also effective in other measurements of experiments. The above process can be realized by the beam splitter as shown in [Figure 5](#f5){ref-type="fig"}. In the experiment, the same polarization for the light beams is required. Realization of Bell-state measurement for classical optical entangled states ---------------------------------------------------------------------------- Bell-state measurement is a key part in the teleportation scheme. In our teleportation scheme, we perform the Bell-state measurement referring to three-photon scheme described in Ref. [@b2] as shown in [Figure 6](#f6){ref-type="fig"}. The marks π/2 and π/4 in [Figure 6](#f6){ref-type="fig"} represent the angle between the axis of HWP and the horizontal direction. The functions of two HWPs are to realize interchange between and polarizations, add a π phase for the component of polarization field. The Jones matrix for the BS is taken in the following form:Two HWPs are put at the output port of the difference. If the input ports are in four Bell-states, the results by the correlation measurement of the first-order field are given in the [table 1](#t1){ref-type="table"}. Taking the antisymmetric state as an example, in the following we give a demonstration on such a result. The antisymmetric Bell state isThe corresponding field isAfter passing through the BS, they becomeConsider the output of the difference, perform interchange between and polarizations and add a π phase for the component of polarization field by the HWPs, we haveFrom the complete incoherent condition and the correlation measurement of the first-order field for two components in Eq.(14), we have:Similarly, consider three symmetric states passing through the above optical element group, we find that all outputs are zero. Here the effect of polarization is considered in the correlation measurement of the first-order field. Author Contributions ==================== Theoretical method is presented by Y.S., the corresponding experiments are performed by X.S. Thus, Y.S. and X.S. contributed equally to this work. In doing the experiments, X.S. get the help of H.Q., X.Z. and Z.Y., the idea and physical analysis are given by X.Z. All authors reviewed the manuscript. Supplementary Material {#s1} ====================== ###### Supplementary Information Supplementary Information This work was supported by the National Natural Science Foundation of China (Grant No. 11274042 and 61421001). ![Experimental setup for CHSH-type Bell inequality violation by using two separable classical light sources.\ E~1~ and E~2~ are two laser beams with different wavelengths. and denote the horizontal and vertical polarization components. (P)BS, (polarizing) beam splitter; HWP, half-wave plate. The first-order correlation measurement is performed between E~ai~ and E~bj~ (i, j = h, v).](srep09175-f1){#f1} ![The correlation functions C(θ~a~,θ~b~) as a function of polarization rotated angle θ~a~ at θ~b~ = 0° (a) and θ~b~ = 45° (b).\ The circle dots and solid lines represent the experimental and theoretical results, respectively. The dashed lines mark the values of θ~a~ to achieve the maximum violations of Bell inequalities.](srep09175-f2){#f2} ![Teleportation scheme showing principles and experimental set-up for the linear polarization case.\ The classical EPR source shown in the bottom plate is the same to that in [Fig. 1](#f1){ref-type="fig"}. Alice and Bob share an ancillary classical entangled states marked by and . Alice performs a joint Bell-state measurement on and the initial state marked by . After Alice has sent the measured result E~ac~ as classical information to Bob, Bob performs the correlation measurement of the first-order field by using and E~ac~. E~\\|\\|~ and represent the transmission and reflection parts as passes through a rotated PBS, ΔI is the difference of the light intensities at two export positions.](srep09175-f3){#f3} ![Experimental (circle dots) and theoretical (solid lines) results from the correlation measurement of the first-order field for the linear polarization case, which are described by the differences of light intensities ΔI as a function of the angle ϕ.\ (a) and (b) correspond to the results for E~\\|\\|~ and , respectively, as the polarization of the initial state θ = 0; (c) and (d) display the corresponding results as θ = π/4.](srep09175-f4){#f4} ![Schematic picture for the first-order field correlation.](srep09175-f5){#f5} ![Design scheme for Bell-state measurement.](srep09175-f6){#f6} ###### The results for Bell-state measurement Bell-state Classical field E~a~ Classical field E~b~ The first-order field correlation ------------ ---------------------- ---------------------- 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But despite the craze, some said that the supermoon had appeared quite similar to other full moons in the past and was fairly "imperceptible," Universe Today reports. In fact, according to a report, the closest full moon in 2017 will only be 0.02 percent farther away than November's supermoon. What is a supermoon? A supermoon occurs when the moon is at its closest point of approach in its orbit around the world. According to NASA, the term supermoon became popular in recent years, referring to a new or full moon that is within 90 percent of its closest approach to the planet, which makes it appear 14 percent bigger and 30 percent brighter in the sky. Since the moon's orbit is elliptical, one side (perigee) is about 30,000 mils closer to Earth than the other (apogee). When the Earth, sun and the moon line up as the moon orbits the Earth (syzygy), and the moon is on the opposite side of the Earth from the sun (perigee-syzygy), a perigee moon or supermoon occurs. The Nov. 14 full moon will be the closest since 1948, and the next time the full moon will come this close again will be on Nov. 25, 2034. The November supermoon is also called Beaver Moon, as it arrives at the time of year when hunters are said to be setting traps on the swamps before they froze over to make sure they will have enough furs to cover up for the winter. Where to see it Stargazers could catch the supermoon on Nov. 14 at 8:52 a.m. EST. To get a better view of the moon, it is recommended to go to the top floor of a building during dusk, facing east.	3.515625	4	[ 0.00250244140625, 0.005035400390625, 0.023681640625, 0.0087890625, 0.0042724609375, -0.00897216796875, -0.0107421875, -0.0023956298828125, -0.0036773681640625, 0.00299072265625, 0.0036163330078125, 0.00958251953125, -0.005584716796875, -0.005126953125, 0.00567626953125, 0.000164031982421875, -0.01483154296875, 0.017333984375, -0.0076904296875, 0.02490234375, 0.0595703125, -0.004730224609375, 0.00555419921875, -0.0142822265625, -0.005706787109375, -0.00054931640625, -0.0030364990234375, 0.00732421875, 0.01202392578125, -0.0198974609375, -0.01708984375, -0.0146484375, -0.03173828125, -0.005645751953125, -0.004547119140625, -0.004180908203125, -0.0036163330078125, 0.01361083984375, -0.0029449462890625, -0.0184326171875, 0.00238037109375, -0.00830078125, 0.00225830078125, -0.017333984375, 0.000652313232421875, 0.005340576171875, 0.003997802734375, 0.011474609375, 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In recent years, movements of construction of a wireless communication network using a flying object such as a satellite and a balloon have been active. The wireless communication network using a flying object has an advantage that, in comparison with a communication network constructed on a surface of the ground, a base station is unlikely to encounter a disaster, for example, by constructing the base station on a flying object, and thereby disaster-resistant property is improved. Further, the wireless communication network using a flying object also has an advantage that a cost for construction such as installation of wiring facilities can be reduced. It is predicted that users of such a wireless communication network using a flying object increase, and with an increase of the users, it is supposed that frequency bands of radio waves used in the wireless communication network are tight. Therefore, as wireless communication used in the wireless communication network using a flying object, attention is paid to free space optics (FSO) using an optical frequency band expected to become markedly broadband, instead of microwaves that are currently mainstream. In order to achieve a large-capacity free space optics system, a speeding-up technique of a bit rate of a transmission signal light and a wavelength division multiplexing technique are required. Further, in a free space optics system, since a signal light is propagated for a long distance between a flying object in midair and the ground, attenuation of the signal light during the propagation is large, and therefore a high-sensitive reception device is required. For the reception device, a technique common to an optical fiber communication technique, specifically, an optical transmission/reception technique using a single mode fiber (SMF) is applied. The reason why the single mode fiber is used in a free space optics system is that an optical transmission/reception technique such as a low-noise and high-gain direct optical amplification technique, a high-sensitive digital coherent reception technique, a high bit-rate transmission/reception technique, and a dense wavelength division multiplexing (DWDM) technique can be used. In a free space optics system using a single mode fiber, it is necessary for a signal light (laser light) propagated in a free space to enter (be coupled with) a core having a small core diameter in the single mode fiber. Therefore, in a free space optics system between a flying object in midair such as an artificial satellite, and a ground station, in order to condense sufficient optical power, a reception device needs to include a telescope having a large aperture diameter. Herein, an aperture of the telescope is equal to or more than several times a spatial coherence radius of a signal light (laser light) propagated in the atmosphere, and therefore the signal light is likely to be affected by turbulence of the atmosphere such as wind. In other words, when passing through a portion where a local fluctuation of a refractive index of the atmosphere caused by a turbulence phenomenon and a thermal phenomenon occurs, a signal light is refracted and the signal light is deflected due to the refraction. Therefore, a disturbance of a beam spot of a signal light condensed by a telescope increases. In this manner, an intensity of a signal light that enters a reception device largely varies due to a disturbance of a beam spot, and therefore, in a free space optics system, a problem that stable communication is difficult occurs. In particular, when a large attenuation (fade) of a signal light due to a large intensity variation occurs, an error or lack of reception data is caused. Therefore, in a free space optics system, a problem that an overhead of forward error correction (FEC) increases and a problem that retransmission processing becomes necessary occur. Such problems cause a decrease in an effective throughput of a free space optics system. As described above, in a free space optics system, due to a disturbance of a wave-front to which a signal light is subjected during atmospheric propagation, a problem that communication becomes unstable may occur. A large number of techniques for solving such the problem have been proposed heretofore. A reception device disclosed in PTL 1 (Japanese Translation of PCT International Application Publication No. 2013-535871) includes a light condensing unit, a wavelength demultiplexer, a plurality of optical detectors, and a signal processing unit. The reception device is configured to collect light on a plurality of individual fiber end faces from the wavelength demultiplexer and converge a signal light to a single output fiber to be input to the optical detector by using a fiber bundle or the like that is gradually thinner. By such a configuration, in the reception device, stable fiber coupling is achieved even against a disturbance of a beam spot. Further, PTL 1 also discloses a configuration in which a core diameter is decreased to a diameter equal to that of a single mode fiber in a tapered shape, and thereby a coupled signal light is converged on a core of the single mode fiber and connection to an optical component adapted to a next-stage single mode fiber is made possible. A communication device that constructs a free space optics system disclosed in PTL 2 (Japanese Registered Patent Publication No. 4701454) includes a light condensing unit, a fiber bundle, a plurality of optical receivers, a plurality of optical transmitters, and a transmission/reception control unit. The communication device is configured to transmit a signal light from the same position as a light condensing position of a signal light received from an opposite device. By this configuration, regardless of deflection of a light condensing system due to an atmospheric fluctuation and a peripheral temperature change, in the opposite device side, a signal light from the communication device is condensed to a signal light emission point. NPL 1 (“Next-generation Extremely Large Optical Infrared Telescope Planning Instructions”) discloses an adaptive optics (AO) technique that measures and corrects distortion of a wave-front of a signal light. In the technique, a wave-front of a reception light distorted due to an atmospheric fluctuation is observed by a wave-front sensor and a wave-front correction element using a micro electro mechanical system (MEMS) or the like is controlled by using the observation result.	3.53125	4	[ 0.0006866455078125, 0.01385498046875, 0.00726318359375, -0.00127410888671875, -0.01458740234375, -0.0203857421875, -0.0068359375, 0.0106201171875, 0.000667572021484375, -0.0052490234375, -0.0084228515625, -0.005401611328125, 0.00701904296875, -0.003814697265625, -0.01214599609375, -0.007171630859375, 0.00098419189453125, 0.013671875, 0.013427734375, 0.01123046875, 0.0286865234375, 0.000415802001953125, -0.00836181640625, -0.005401611328125, 0.000812530517578125, -0.01251220703125, 0.01226806640625, 0.0048828125, -0.012451171875, -0.0137939453125, 0.007080078125, 0.00144195556640625, -0.01507568359375, 0.0064697265625, 0.00970458984375, -0.011474609375, 0.015625, -0.000690460205078125, 0.00433349609375, 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The drive system for a rotating apparatus (such as a centrifuge instrument) typically includes a shaft attached at one end to a motive force (e. g., an electric motor). The shaft supports a load somewhere along its length. One inherent property of such a drive system is load imbalance. Even a very small imbalance in the otherwise symmetrical mass distribution about the drive shaft can cause damaging vibrations. The magnitude of the imbalance places a load on the bearings. This problem can be addressed by providing a degree of flexibility to the drive shaft. However, as this rotating apparatus accelerates to its operating speed the system passes through several critical speeds. A thin, elongate shaft rotating about its longitudinal axis possesses certain natural frequencies of vibration that become apparent at these critical speeds. Passage through a critical speed thus causes the drive system to vibrate, which in turn magnifies the load imposed on the bearings. This increase in load can significantly reduce the life of the bearing. In the example of a centrifuge instrument the vibration may also have a detrimental effect on the sample that is being processed within the rotor of the instrument. Several methods have been proposed in the art to solve the problem of vibration generated during passage of a drive system of a rotating apparatus through a critical rotational speed. One solution is to attempt to damp the vibrations imposed on the system. U.S. Pat. No. 5,026,341 (Giebeler) is an example of a rotating system for use in a centrifuge instrument that restricts the deflection of the shaft, thus damping vibration. Another solution, exemplified by the arrangement disclosed in U.S. Pat. No. 4,236,426 (Meinke et al.), is to alter the physical properties of the drive system in a speed-dependent fashion. As a result, for a first portion of the speed regime of the apparatus, the stiffness of the system is such that the critical speed lies well beyond a predetermined speed threshold. However, once the speed threshold is crossed the stiffness of the system is dynamically altered such that the critical speed of the modified drive lies at a speed that is well below the predetermined threshold. Thus, as the apparatus accelerates through its fill speed regime to its operating speed the critical speeds associated with both the original and the modified drives are avoided. In an arrangement as shown in the Meinke et al. patent, springs, dampers and/or masses are actively coupled and uncoupled in response to the changes in the deflection of the shaft. This coupling and uncoupling has the effect of altering the critical rotational speeds. Implementation of either of the above-described expedients usually requires a complex mechanism to effect the interaction between rotating and non-rotating parts of the drive system. In either case, technical difficulties can result. Therefore, in view of the foregoing it is believed advantageous to provide an arrangement of the type which dynamically alters the stiffness of the drive system, yet which does so without undue mechanical complexity.	3.109375	3	[ -0.007110595703125, 0.005126953125, 0.0059814453125, -0.003631591796875, -0.01611328125, -0.021484375, -0.00531005859375, 0.0015411376953125, -0.01043701171875, -0.00396728515625, 0.009765625, 0.008056640625, -0.01361083984375, -0.006866455078125, -0.00872802734375, -0.00836181640625, -0.0034942626953125, 0.005096435546875, 0.0076904296875, 0.005340576171875, 0.052001953125, 0.00592041015625, 0.003936767578125, 0.00157928466796875, -0.0001926422119140625, -0.00634765625, 0.00634765625, 0.006317138671875, -0.01129150390625, 0.01263427734375, 0.0159912109375, 0.004547119140625, -0.022705078125, 0.0128173828125, -0.00604248046875, -0.01263427734375, 0.0177001953125, 0.004638671875, 0.00787353515625, -0.0230712890625, -0.0037841796875, -0.00750732421875, 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Pediatric migraine: recognition and treatment. The diagnosis of migraine headache in childhood rests on criteria similar to those used in migraine in adults. It is important, however, to appreciate several fundamental differences. These differences include the duration of attack, which is often far shorter than in an adult, and the location of the attack, which may be bilateral in many children. The treatment of children and adolescents with migraines includes treatment modalities for acute attacks, preventive medications when the attacks are frequent, and biobehavioral modes of therapy to address long-term management of the disorder. The controlled clinical trials of medications in pediatric migraine have suffered from high placebo response rates that may be related to the sites conducting the study (ie, headache specialist vs clinical research organizations). The medications have proved to be safe in the pediatric age group. Treatment modalities for acute migraine include over-the-counter nonsteroidal anti-inflammatory drugs (NSAIDs), as well as the oral triptans such as sumatriptan succinate, rizatriptan benzoate, and zolmitriptan and the nasal spray formulations of sumatriptan and zolmitriptan. Subcutaneous sumatriptan and parenteral dihydroergotamine have also been used limitedly. Preventive treatment for patients with frequent or disabling migraines (or both) includes the antidepressants amitriptyline hydrochloride and nortriptyline hydrochloride, the anticonvulsants divalproex sodium and topiramate, and the antihistaminic agent cyprohepatine hydrochloride. Biobehavioral approaches aimed at addressing the fundamental lifestyle issues and nonpharmacologic approaches to management are fundamental to long-term success.	3.578125	4	[ 0.005950927734375, -0.000202178955078125, -0.0031890869140625, -0.0031280517578125, -0.0191650390625, -0.01043701171875, -0.01043701171875, -0.0166015625, 0.00750732421875, -0.0269775390625, 0.005126953125, -0.000690460205078125, -0.0023956298828125, 0.004119873046875, -0.0130615234375, -0.00823974609375, 0.005157470703125, -0.00189208984375, 0.00148773193359375, -0.01031494140625, 0.00701904296875, 0.0024871826171875, -0.002044677734375, -0.005126953125, 0.00213623046875, 0.008544921875, 0.006439208984375, -0.00445556640625, 0.0024566650390625, 0.00982666015625, 0.00176239013671875, -0.015625, -0.0135498046875, -0.028076171875, 0.0018768310546875, 0.003448486328125, 0.01214599609375, -0.00933837890625, -0.0208740234375, 0.017578125, -0.015380859375, -0.0062255859375, 0.0162353515625, -0.0076904296875, 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Q: Darkest matter on Earth ("pure black") What is (for a human's eyes) the natural or synthetical matter on Earth (i.e. not in Space) that emits the least quantity of visible photons while being lightened by sunlight? In this matter, how is light converted? Invisible wavelengths (ultraviolet, X-rays)? Heat? A: "Vantablack, made out of carbon nanotubes, is designed by Surrey NanoSystems and absorbs 99.96% of all light that hits it. 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A scanning probe microscope (SPM) brings a pointed probe close to a sample to detect the interaction between the probe and the sample (a tunnel current, an interactive force, or the like). The scanning probe microscope then feedback-controls the distance between the probe and the sample so as to keep the interaction constant. Moreover, the SPM scans the probe (or the sample) in the horizontal direction with the feedback control maintained. Thus, the probe (or the sample) moves up and down so as to trace recesses and protrusions on the sample. An image of the recesses and protrusions on the surface of the sample can be obtained by recording the track of the feedback scanning with respect to the horizontal position. A known example of the SPM is an atomic force microscope (AFM). The AFM detects an interactive force acting between the probe and the sample. The AFM then feedback-controls the distance between the probe and the sample so as to keep the interactive force constant. The AFM uses a cantilever with a pointed probe provided at the tip thereof, as a force detector. When the probe is brought closer to the sample, the cantilever is displaced by the interactive force acting between the probe and the sample. This type of AFM configured to detect the interactive force based on the amount of displacement is called a contact mode AFM or a static mode AFM. On the other hand, a type of AFM configured to mechanically excite the cantilever at a frequency close to the resonant frequency thereof is called a dynamic AFM. The dynamic AFM detects the interactive force acting between the probe and the sample, based on a variation in vibration amplitude, frequency, phase caused by the interactive force. AFMs detecting the interactive force using the amplitude, frequency, and phase are called an AM-AFM, an FM-AFM, and a PM-AFM, respectively. The conventional dynamic mode AFM is disclosed in, for example, Japanese Patent Laid-Open No. 2004-226237. This document discloses an example of the FM-AFM. FIG. 1 shows a general configuration of a dynamic mode AFM. An AFM 101 includes a cantilever 103, a sample stage 105, a scanner 107, and an excitation unit 109. The scanner 107 is, for example, a piezo actuator and moves a sample on the sample stage 105 in an X direction, a Y direction, and a Z direction to scan a sample and the cantilever 103 relative to each other. The excitation unit 109 is also, for example, a piezo actuator and excites the cantilever 103. For example, an amplifier configured to drive an actuator is omitted from FIG. 1. An excitation and detection circuit 111 is configured to provide an excitation control function and a function to detect an interactive force. The excitation and detection circuit 111 applies an excitation signal to the excitation unit 109 to excite the cantilever 103. Furthermore, the excitation and detection circuit 111 detects, as the amount of the interaction between the probe and the sample, the amplitude, frequency, or phase of a displacement signal from the cantilever 103 detected by the sensor 113. The detected value is output to a feedback circuit 115 as a feedback signal and used to control the vertical position of the scanner 107. As a result, a feedback loop is formed which keeps the distance between the probe and the sample constant. As described above, in the present specification, a circuit functioning as an excitation control circuit and an interaction detection circuit is referred to as the “excitation and detection circuit”. Several types of methods are available for implementing the excitation and detection circuit. The excitation and detection circuit can be roughly classified into an analog type and a digital type. The digital type is now mainly used because the specifications of the digital type can be flexibly changed and because the digital type can implement complicated signal processing. FIG. 2 shows an example of an implemented excitation and detection circuit of a conventional digital type. The configuration in FIG. 2 corresponds to the AM-AFM and the PM-AFM and generates an excitation signal and detects an amplitude signal and a phase difference signal. The amplitude signal indicates the vibration amplitude of the cantilever. The phase difference signal indicates the difference in phase between the excitation signal for the cantilever and a displacement signal from the cantilever. As shown in FIG. 2, an excitation and detection circuit 121 includes a DDS (Direct Digital Synthesizer) 123 and a lock-in amplifier 125. The DDS 123 corresponds to an excitation control circuit. The lock-in amplifier 125 corresponds to a detection circuit for the amplitude and phase difference. In FIG. 2, the DDS 123 generates an excitation signal cos(2πft) that varies at an excitation frequency f. The DDS 123 holds sine-wave output values with respect to the phase, in the form of a lookup table. A sine wave signal is obtained by interpolating discreet values in the lookup table. The signal is not only output as the excitation signal for the cantilever but is also utilized as a reference signal for the lock-in amplifier 125 formed of a digital circuit. The lock-in amplifier 125 is a two-phase digital lock-in amplifier. A displacement signal Acos(2πft+φ) from the cantilever is input to the lock-in amplifier 125. The excitation signal cos(2πft) is also input to the lock-in amplifier 125 as the reference signal as described above. The reference signal is input to a 90° phase shift circuit (for example, a Hilbert conversion circuit) and a delay circuit, which then convert the signal into sin(2πft) and cos(2πft), respectively. These signals are converted into X=Acos(φ) and Y=Asin(φ), respectively, through a multiplication circuit and an LPF (Low Pass Filter). The multiplication circuit multiples each of the signals by the input displacement signal Acos(2πft+φ). The LPF removes high frequency components from the signals. Then, a vector calculation circuit calculates the absolute value R and argument θ of a complex input X+jY. The absolute value R is (X2+Y2)1/2, and the argument θ is tan−1(Y/X). The absolute value R corresponds to the amplitude A of the displacement signal. The argument θ corresponds to the phase difference φ between the displacement signal and the excitation signal. Thus, R and θ are output as the amplitude signal A and the phase difference signal φ, respectively. The configuration in FIG. 2 corresponds to an AM-AFM mode and a PM-AFM mode. In the AM-AFM mode, the amplitude signal A is output as a feedback signal and used for feedback control. The feedback control is performed such that the amplitude signal A equals a target amplitude. In the PM-ADM mode, the phase difference signal φ is output as a feedback signal and used for feedback control. In this case, the feedback control is performed such that the phase difference signal φ equals a target phase difference. Now, the configuration of the excitation and detection circuit for the FM-AFM will be described with reference to FIG. 3 and FIG. 4. FIG. 3 is a diagram based on which the principle of the FM-AFM will be described, and illustrates the characteristics of amplitude and phase of the cantilever. In an upper graph in FIG. 3, the axis of abscissas indicates frequency, and the axis of ordinate indicates the amplitude of the cantilever. In a lower graph in FIG. 3, the axis of abscissas indicates the frequency, and the axis of ordinate indicates the difference in phase between the excitation signal for the cantilever and displacement signal from the cantilever. As shown by a dotted line in the upper graph in FIG. 3, the resonant frequency f of the cantilever varies (shifts) as a result of the interaction between the cantilever and the sample. In FIG. 3, the amount of variation in resonant frequency is indicated by Δf. Furthermore, as shown in the lower graph, when the cantilever vibrates at the resonant frequency, the phase difference φ between the excitation signal and the displacement signal is 90°. Thus, the FM-AFM sets a target value for the phase difference φ to 90°, and controls the excitation signal such that the phase difference φ equals the target value. This excitation control is achieved by a phase locked loop (PLL) circuit and is such that even if the resonant frequency of the cantilever is varied by the interaction, the cantilever continues to vibrate at the resonant frequency. During this control, a variation in resonant frequency Δf is detected. Then, the feedback control is performed so as to keep the variation in resonant frequency Δf constant. FIG. 4 shows an example of an implemented excitation and detection circuit corresponding to the FM-AFM. The excitation and detection circuit generates an excitation signal and detects a frequency signal. The frequency signal is indicative of a variation in the resonant frequency of the cantilever caused by the interaction between the cantilever and the sample as described above. As shown in FIG. 4, an FM-AFM excitation and detection circuit 131 includes a proportional integral (PI) control circuit 137 in addition to a DDS 133 and a lock-in amplifier 135 (two-phase digital lock-in amplifier). An excitation signal cos(2πft) output by the DDS 133 is input to the lock-in amplifier 135 as a reference signal. Furthermore, a displacement signal Acos(2πft+φ) from the cantilever is input to the lock-in amplifier 135. The lock-in amplifier 135 has a configuration similar to that of the lock-in amplifier 125 in FIG. 2 to output the phase difference φ between the excitation signal and the displacement signal. Here, the lock-in amplifier 135 functions as a multiplying phase comparator to perform phase comparison based on multiplication of the displacement signal. A phase difference φ generated by the lock-in amplifier 135 is input to a PI control circuit 137. The PI control circuit 137 controls an output 2πΔfT (reference character T denotes a sampling period for input and output signals) such that the input phase difference φ equals a target value φ0. The output 2πΔfT is input to the DDS 133 to vary the frequency f of an output signal (excitation signal) cos(2πft) of the DDS 133. The frequency f varies around the free-running frequency f0 (an oscillation frequency obtained when the input is 0) of the DDS by Δf. In the configuration in FIG. 4, the DDS 133, the lock-in amplifier 135, and the PI control circuit 137 form the phase locked loop (PLL) circuit. The PI control circuit 137 functions as a loop filter for the PLL circuit. The PLL circuit varies the value of the frequency f of the excitation signal so that the frequency of the displacement signal equals that of the excitation signal, that is, f=f0+Δf. Thus, an output value from the PI control circuit 137 is proportional to a variation in the frequency of the displacement signal. Thus, the output value from the PI control circuit 137 is output as the frequency signal. Furthermore, the difference in phase between the displacement signal and the excitation signal can be adjusted by varying the target value φ0 for the PI control circuit 137. As described with reference to FIG. 3, the FM-AFM sets the target phase difference to 90°. Thus, the phase difference φ is kept at 90°, and the cantilever vibrates at the resonant frequency. Even if the resonant frequency of the cantilever is varied by the interaction between the cantilever and the sample, the cantilever continues to vibrate at the resonant frequency. The frequency signal has a value indicative of a variation (shift) Δf in the resonant frequency of the cantilever. The frequency signal is used for feedback control. The conventional AFM excitation and detection circuit has been described. There is still room to improve of the conventional circuit configuration as described below. In the conventional technique illustrated in FIG. 2, the lock-in amplifier functions as a multiplying phase comparator and internally compares the excitation signal with the displacement signal by multiplication. This leads to generation of an unwanted harmonic component. More specifically, an output from the multiplication circuit in the lock-in amplifier contains a component of the difference in frequency between input signals and a component of the sum of the frequencies of the input signals. The sum component corresponds to the unwanted harmonic component. The harmonic component cannot completely be removed even by the LPF arranged after the lock-in amplifier. Such a residual harmonic component may not only distort an output waveform but also affect the feedback control as described below. The AFM forms a feedback loop for control of the probe-sample distance, and the excitation and detection circuit is present in the feedback loop as shown in FIG. 1. A signal in which the harmonic component is mixed in the lock-in amplifier is used in the feedback loop. In this case, a feedback gain needs to be limited to a small value in order to avoid oscillation at the frequency of the harmonic component. This conventionally constitutes a factor preventing quick and stable feedback control from being achieved. In the FM-AFM circuit configuration shown in FIG. 4, as is the case with the circuit in FIG. 2, the lock-in amplifier functions as a multiplying phase comparator, leading to generation of an unwanted harmonic component. In particular, in the FM-AFM, the harmonic component not only limits the feedback gain but also works against the PLL circuit. This will be described below. In the FM-AFM configuration shown in FIG. 4, the lock-in amplifier is a part of the PLL circuit. Thus, the lock-in amplifier (multiplying phase comparator) generates an unwanted harmonic component in the loop in the PLL circuit. The harmonic component cannot completely be removed even by the LPF arranged after the lock-in amplifier. In particular, the LPF is present in the loop in the PLL and is thus subject to another restriction; the LPF cannot be designed independently of the response characteristics of the PLL. Thus, removal of the harmonic component in the FM-AFM is more difficult than in the AM-AFM and the PM-AFM. Because of the residual harmonic component, an increase in the gain of the PLL causes the PLL circuit to oscillate at the frequency of the residual harmonic component. Thus, in the conventional technique, the gain of the PLL is limited, preventing the frequency from being detected quickly and stably. As described above, in the FM-AFM, disadvantageously, the harmonic component limits not only the feedback gain of the whole AFM but also the gain of the PLL.	3.203125	3	[ -0.00299072265625, 0.003662109375, 0.01068115234375, -0.01239013671875, -0.005401611328125, -0.0169677734375, -0.0096435546875, -0.0135498046875, -0.00994873046875, -0.000606536865234375, 0.0048828125, 0.0274658203125, -0.052001953125, -0.0023345947265625, -0.0125732421875, 0.0133056640625, -0.002716064453125, 0.00958251953125, 0.01422119140625, -0.0181884765625, -0.02099609375, -0.0038604736328125, 0.00689697265625, 0.00677490234375, 0.002410888671875, 0.006622314453125, -0.0087890625, 0.007415771484375, -0.01519775390625, -0.003326416015625, -0.0223388671875, -0.0086669921875, -0.0203857421875, -0.00579833984375, -0.004180908203125, -0.008544921875, 0.00421142578125, 0.01531982421875, -0.0230712890625, 0.003875732421875, -0.00154876708984375, -0.0072021484375, 0.0186767578125, -0.01275634765625, 0.002777099609375, 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Although the Universe may seem spacious most galaxies are clumped together in groups or clusters and a neighbour is never far away. But this galaxy, known as NGC 6503, has found itself in a lonely position, shown here at ... European aircraft and aerospace giant Airbus has unveiled plans for a reusable space rocket launcher that should be ready in 2025, which the firm says will be radically different from the concept of rival US firm Space X. Skygazers at northern latitudes are familiar with the W-shaped star pattern of Cassiopeia the Queen. This circumpolar constellation is visible year-round near the North Star. Tucked next to one leg of the W lies a modest ... Space Space is the boundless, three-dimensional extent in which objects and events occur and have relative position and direction. Physical space is often conceived in three linear dimensions, although modern physicists usually consider it, with time, to be part of the boundless four-dimensional continuum known as spacetime. In mathematics spaces with different numbers of dimensions and with different underlying structures can be examined. The concept of space is considered to be of fundamental importance to an understanding of the universe although disagreement continues between philosophers over whether it is itself an entity, a relationship between entities, or part of a conceptual framework. Many of the philosophical questions arose in the 17th century, during the early development of classical mechanics. In Isaac Newton's view, space was absolute - in the sense that it existed permanently and independently of whether there were any matter in the space. Other natural philosophers, notably Gottfried Leibniz, thought instead that space was a collection of relations between objects, given by their distance and direction from one another. In the 18th century, Immanuel Kant described space and time as elements of a systematic framework which humans use to structure their experience. In the 19th and 20th centuries mathematicians began to examine non-Euclidean geometries, in which space can be said to be curved, rather than flat. According to Albert Einstein's theory of general relativity, space around gravitational fields deviates from Euclidean space. Experimental tests of general relativity have confirmed that non-Euclidean space provides a better model for explaining the existing laws of mechanics and optics.	3.546875	4	[ 0.0179443359375, -0.0128173828125, 0.01007080078125, -0.00164794921875, -0.01519775390625, -0.0030364990234375, -0.007049560546875, -0.004730224609375, -0.0038909912109375, 0.019287109375, -0.0115966796875, 0.00799560546875, 0.0059814453125, 0.003021240234375, 0.006622314453125, -0.0107421875, -0.01385498046875, 0.0390625, 0.019775390625, 0.0157470703125, 0.0031280517578125, 0.0177001953125, -0.01239013671875, 0.0036468505859375, -0.0211181640625, 0.01458740234375, 0.0169677734375, -0.00848388671875, 0.0157470703125, 0.0120849609375, 0.00927734375, 0.0062255859375, -0.038818359375, -0.005340576171875, 0.005950927734375, -0.0167236328125, 0.00408935546875, 0.001678466796875, -0.0247802734375, -0.00640869140625, 0.0120849609375, -0.01708984375, -0.016357421875, 0.01324462890625, 0.00390625, 0.0106201171875, 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In a find that sheds light on how Earth-like planets may form, astronomers have reported finding the first evidence of small, sandy particles orbiting a newborn solar system at about the same distance as the Earth orbits the sun. "Precisely how and when planets form is an open question," said study co-author Christopher Johns-Krull, assistant professor of physics and astronomy at Rice University. "We believe the disk-shaped clouds of dust around newly formed stars condense, forming microscopic grains of sand that eventually go on to become pebbles, boulders and whole planets." In previous studies, astronomers have used infrared heat signals to identify microscopic dust particles around distant stars, but the method isn't precise enough to tell astronomers just how big they become, and whether the particles orbit near the star, like the Earth does the sun, or much further away at a distance more akin to Jupiter or Saturn. In the new study, Johns-Krull and co-authors in the United States, Germany and Uzbekistan used reflected light from the sand itself to confirm the Earth-like orbit of grainy particles around a pair of stars called KH-15D in the constellation Monoceros. The stars are about 2,400 light years from Earth in the Cone Nebula, and they are only about 3 million years old, compared to the sun's 4.5 billion years. "We were attracted to this system because it appears bright and dim at different times, which is odd," Johns-Krull said. The researchers found that the Earth has a nearly edge-on view of KH-15D. From this perspective, the disk blocks one of the stars from view, but its twin has an eccentric orbit that causes it to rise above the disk at regular intervals. "These eclipses let us study the system with the star there and with the star effectively not there," Johns-Krull said. "It's a very fortuitous arrangement because when the star is there all the time, it's so bright that we can't see the sand." The team conducted both photometric and spectrographic analyses of data collected during the past 12 years from a dozen observatories, including the McDonald Observatory in west Texas, the Keck Observatory in Hawaii and the VLT on Mount Paranal in Chile. "Because of how the light is being reflected there are opportunities to make observations about the chemical composition of these sand-like particles," said co-author William Herbst, an astronomer at Wesleyan University in Middletown, Conn. "That's very exciting because it opens up so many doors for new type of research on this disk." The report is to be published online by the journal Nature. Co-authors include Catrina Hamilton of Dickinson College; Katherine LeDuc of Wesleyan University; Joshua Winn of the Massachusetts Institute of Technology; Reinhard Mundt of the Max Planck Institute for Astronomy in Heidelberg, Germany; and Mansur Ibrahimov of the Ulugh Beg Astronomical Institute in Tashkent, Uzbekistan.The research was funded by NASA and the Keck Foundation.	4.125	4	[ 0.00360107421875, -0.010009765625, 0.015869140625, 0.0021514892578125, -0.006805419921875, -0.01031494140625, 0.001190185546875, -0.01312255859375, -0.01043701171875, -0.00860595703125, 0.00927734375, 0.0216064453125, -0.0218505859375, -0.00433349609375, -0.0029144287109375, -0.00653076171875, 0.00958251953125, 0.008544921875, 0.017333984375, 0.0218505859375, 0.01171875, 0.00084686279296875, -0.006072998046875, -0.00823974609375, -0.0018157958984375, 0.01171875, 0.0035552978515625, -0.018310546875, 0.0002899169921875, 0.0019989013671875, -0.005828857421875, 0.0174560546875, -0.0279541015625, 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Structure Use parentheses when instantiating classes regardless of the number of arguments the constructor has. Declare class properties before methods. Declare public methods first, then protected ones and finally private ones. The exceptions (when using PHPUnit) to this rule are the class constructor and the setUp and tearDown methods of PHPUnit tests, which should always be the first methods to increase readability. Traits Traits are treated as classes. Ternary Operator Ternary operators are permissible when the entire ternary operation fits on one line. Longer ternaries should be split into if else statements. Ternary operators should not ever be nested. Optionally parentheses can be used around the condition check of the ternary for clarity: Most IDEs even nowadays can't show start/end for keywords, with brackets it always works in pretty much every IDE, though. If you intend to use the keywords in template files, you should at least be consistent and use them througout the files. But in general it is better to also stick to curly brackets here for consistency throughout the codebase. PHP Open Tags Always use <?php or <?= instead of <?. The <?= form should be used for echoing values of simple variables while the <?php form can be used for more complex code. The short form is supported by the newest PHP versions as well and it makes your files less verbose, thus easier to read. It doesn't even require the semicolon (;) so feel free to omit it. This <?= $x ?> way. If you want to comment it out then you can do it easily: This <?//= $x ?> way. Commenting out with <!-- --> should be avoided as it is then visible in the resulting HTML output. Comparison Always try to be as strict as possible. If a non-strict test is deliberate it might be wise to comment it as such to avoid confusing it for a mistake. For testing if a variable is null, it is recommended to use a strict check: Multi-line declaration/condition/concatenation Multi-line control structures should have the parentheses in their own lines (similar to classes and methods): if ( ($a==$b)&& ($b==$c)\|\| (Foo::CONST==$d)) {$a=$d;} Careful with deep arrays One mistake that often gets made: $foo= [[0,1, 2], 3, 4]; This would effectively change all lines (and their indentation), if the array structure got normalized. Arrays also need to minimize effects on the resulting diff, and as such indentation must always be the right one: $foo= [[0,1, 2 ], 3, 4]; for example, max. normalized as: $foo= [ [0,1,2 ],3,4]; As you can see, entries like 0 would not need any change on reorganizing, thus reducing overhead in work and making diffs easier to read as they only show actual changes made. Typehinting Arguments that expect objects, arrays or callbacks (callable) can be typehinted. We only typehint public methods, though, as typehinting is not cost-free: Avoid no-op methods The first would allow no-ops like $this->foo() which does not do any operation at all. So semantically this makes no sense. In this case no default value may be used and a first argument is actually required for the first if statement to make sense ($this->foo($requiredArgument)). You can still pass null, of course, to break out early. Default values may only be used if their usage does make this method still do an operation (apart from returning early). Avoid private for class methods/properties Most of the time private is used too eagerly, where protected would suffice. Allow extending classes to extend the code. Don't assume it doesn't have to. This is especially important for frameworks or vendor libraries that people would like to enhance or customize in their applications. In case you are acquainted with the "Open/Close Principle", it is in some cases OK to use private to define clear public interfaces for classes. Underscores for Private/Protected It is not directly disallowed in PSR-2 to have the _ and __ visibility prefixes. But it says one has a good reason to use them. As most IDEs still don't really clearly display (in colors?) the difference between public, protected and private, the following would be difficult to read: Note that __ is also used for magic calls, and as such this recommendation is best used with the above hint of not using private visibility in your code. Otherwise please disregard and make sure you use an IDE that can display them properly. Using underscores with a lot of private methods will probably be worse than sticking to the PSR-2 recommendation. Return void vs null @return void shall be used to document when a method is expected not to return anything, and when there is just a return; as "early return". Explicitly returning with return null; or return $this->foo(); shall be documented be as @return null etc. HTML All tags and attributes are lowercase. CSS Definition ideally as dashed name: class: .some-class-name id: #some-id-to-an-element Both with lowercase characters (although classes are not case-sensitive, id's are!), the separator is minus [-]. You can use underscore [_] if it makes the separation of the identifier and the record id easier. E.g. my-id_33. It will become necessary to do so if you use UUIDs (which contain minus chars). Note: ids should be unique on the current page - so don't use them for iterating elements. In general all styling should be class based. Ids are often abused for that. But they usually serve the purpose of being identifiable via JS. So they should ideally be mainly used for dynamic JS scripts. Do not name the fields after their style, but after the function/meaning - as the style can change and will result in things like .red { color: yellow;}. JS Ideally, JS related classes are prefixed with js- to separate them from the rest of the CSS and styling related class names: <divclass="js-widget-toggle some-styling-class">...</div> Further considerations While so far the main focus was on the developer (readability), there are some additional optional guidelines that can help to further reduce diff size on code modification (maintainability). Those can and should be automated, though, as there is no point in forcing the developer to take care of those manually. The main idea is to keep each line independant from the others so removing or adding lines has minimal impact. Multi-line arrays Arrays that span across multiple lines can have a trailing comma to make sure that adding new rows does not change the previous row, as well. $array= ['first','second', // Note the trailing comma]; Multi-line logic For longer logic (method calls, operations) it can be helpful to put the trailing semicolon at the next line. 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Many restaurants, and especially fast food restaurants, prepare food in advance so that they can meet the daily fluctuations in demand that occur around breakfast time, lunch time, or dinner time. Food prepared in advance must be stored safely until it is delivered to the consumer. For many food products this means keeping the food product above a certain minimum threshold temperature to prevent spoilage. For other food products, it means keeping the food frozen or chilled. Either way, the food products need to be heated and held at an elevated temperature before being served to consumers. Although many systems exist to warm or heat food, many of these suffer from a number of drawbacks. For example, infrared (IR) heat lamps not only heat the food, but they also heat the surrounding environment. This can result in increased air conditioning costs for the restaurant. This problem may be exacerbated when the food products are in metal foil packaging since the metal foil may have a tendency to reflect the IR radiation away from the food product and into the surrounding environment. Furthermore, IR lamps tend to become quite hot, which poses a burn risk to restaurant employees and/or customers. Although warm air convection systems do not have many of the problems associated with IR lamps, warm air convection systems often cause food products to dry out. Both IR and warm air convection systems tend to steadily consume power regardless of how many food products are currently being heated. It would be desirable to provide an improved system for warming food that is energy efficient, safe, and effective. In one embodiment described herein, an induction heating system is used to warm food. The food may be packaged in food packaging that includes a current conducting material. 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A conventional technique for coating a phosphor on an LED, as shown in FIG. 1, includes directly applying a polymer material 20 such as epoxy, etc., into which the phosphor is mixed, onto an LED 10, and then, curing the polymer material 20. The conventional method of coating a phosphor on an LED has a problem that the polymer material 20 including the phosphor cannot be easily patterned. Therefore, in the conventional phosphor coating method, the phosphor must be applied to the entire surface after completion of wire bonding. In this case, when the LED to which the phosphor is applied cannot have desired performance (for example, in color, uniformity of color, etc.), the LED, which is expensive due to the wire bonding, is wasted, and thus, the overall manufacturing cost increases. In addition, the conventional method of coating a phosphor on the LED 10 is not appropriate for mass production. More specifically, in the conventional phosphor coating method, since the polymer material 20 including the phosphor must be separately coated onto each LED, the coating is expensive. Further, the conventional method of coating a phosphor on the LED 10 has a problem in that the thickness of the polymer material 20 including the phosphor cannot be easily adjusted. When the thickness of the polymer material 20 including the phosphor increases, intensity of light having a frequency varied by the phosphor increases, and when the thickness of the polymer material 20 including the phosphor decreases, intensity of light having a frequency varied by the phosphor decreases. Therefore, since the thickness of the polymer material 20 including the phosphor is an important factor for determining colors finally obtained from the LED 10, the thickness must be precisely controlled. In particular, since the light is emitted from side surfaces of the LED 10 as well as an upper surface thereof, the thickness of the polymer material 20 including the phosphor disposed on the side surfaces of the LED 10 as well as the thickness of the polymer material 20 including the phosphor disposed on the upper surface of the LED 10 must be precisely controlled. Furthermore, since the polymer material 20 including the phosphor is applied onto the LED 10 to a non-uniform thickness in the conventional method of coating a phosphor on the LED 10, uniform colors cannot be obtained. For example, when a white light is obtained by mixing a blue light emitted from a blue LED 10 and a yellow light obtained by a yellow phosphor, the white light with yellow color is transmitted to an observer 1 of FIG. 1 since the thickness of the polymer material 20 including the phosphor is large, and the white light with blue color is transmitted to an observer 2 of FIG. 1 since the thickness of the polymer material 20 including the phosphor is small.	3.078125	3	[ 0.0013427734375, -0.01177978515625, 0.00927734375, 0.0186767578125, -0.00848388671875, -0.0267333984375, 0.0025482177734375, 0.0157470703125, -0.00982666015625, 0.002899169921875, 0.01361083984375, 0.0028076171875, -0.0022125244140625, 0.0057373046875, 0.00872802734375, 0.005950927734375, -0.007476806640625, 0.01806640625, 0.0172119140625, 0.02001953125, 0.058349609375, -0.004119873046875, -0.0179443359375, 0.011474609375, -0.01007080078125, -0.017822265625, 0.01153564453125, 0.01177978515625, 0.021728515625, 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GRADES OR AGES: Grade 5. SUBJECT MATTER: Social studies; economic development of the United States and Canada. ORGANIZATION AND PHYSICAL APPEARANCE: The major portion of the guide, which develops the unit, is laid out in three columns, one each for topics, activities, and materials. Other sections are in list form. The guide is mimeographed and staple-bound with a paper cover. OBJECTIVES AND ACTIVITIES: General objectives for the unit are listed on the first page. Each group of activities in the second column is related to a topic in the first column. INSTRUCTIONAL MATERIALS: Each group of materials listed in the third column is related to one or more activities. In addition, three appendixes contain curriculum materials. STUDENT ASSESSMENT: A one-page section entitled"Evaluation" lists ideas students should understand and skills they should possess by the end of the unit. OPTIONS: The guide is prescriptive as to course content and timing. Activities and materials listed are optional. Also, a short section lists several supplemental activities. 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Identification and differentiation between colored pencils. With pencils of any color, the first step certainly involves visual examination to distinguish between the color tints and to study the quality of the stroke itself. In many instances by this step alone, 2 pencils can be distinguished if they are the product of 2 different manufacturers. In other words, the most useful of all tests is the visual examination. In the case of red pencils, infrared luminescence reveals significant information and should be resorted to in those instances where two questioned strokes are extremely similar. Study under ultraviolet radiation may also help to establish similarities or differences which are not readily discernible by visual examination. However, reflected infrared examination and study with dichroic filters have no particular value when dealing with red pencil although chemical spot testing may be of some assistance. In the case of blue pencils, a number of brands absorbs infrared radiation to a different extent and some give off distinctive infrared luminescence, so that these 2 tests can assist in distinguishing between certain similar colors or tints. Also, study through dichroic filters has value. Thus, the combination of these 3 tests can be of some advantage, but in most instances, particularly with dark blues, examination under ultraviolet radiation is not particularly helpful. Chemical spot testing has some limited advantages but generally only in combination with all other tests. In the case of green pencils, the same pattern of testing may be used as with blues. Many of the greens absorb infrared rays and some have bright infrared luminescence. Ultraviolet radiation can cause certain greens to fluoresce in a distinctive way. Thus, with each color studied, differences can be revealed and similarities established. Colored pencils are a distinct group of writing instruments. Within any color classification, there is a variety of shades or tints. Although it is not psosible to determine the make of pencil used in any particular writing, it is possible under many circumstances to distinguish between the work of different makes and grades of red, blue and green pencils, as well as other colors which have not been covered by this paper. While visual examination will separate the many different makes, other tests are described which will further assist in grouping or separating colored writing strokes. For a number of reasons, and particularly because of manufacturing procedures of different companies, not every make of pencil is distinctive, but there has been found to be a definite variety within each color group, and many makes are distinguishable.	3.140625	3	[ 0.00180816650390625, 0.00083160400390625, 0.0027618408203125, 0.00506591796875, -0.0057373046875, -0.009033203125, -0.0169677734375, -0.0078125, -0.00531005859375, -0.0108642578125, -0.01025390625, 0.01251220703125, -0.0341796875, -0.0017547607421875, -0.000637054443359375, -0.000614166259765625, -0.00023651123046875, 0.007293701171875, -0.01416015625, -0.00360107421875, 0.0235595703125, 0.010009765625, 0.00592041015625, 0.004241943359375, -0.0228271484375, -0.00238037109375, -0.003448486328125, -0.013427734375, 0.017578125, -0.007537841796875, 0.005645751953125, -0.005340576171875, -0.035400390625, -0.000308990478515625, 0.01043701171875, -0.003875732421875, 0.0289306640625, 0.002471923828125, 0.0164794921875, 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Toronto: In a bid to determine whether distant stars with planets orbiting them can harbour life, a global team of astronomers has discovered a new way to measure the pull of gravity at the surface of distant stars. Knowing the surface gravity of a star is essentially knowing how much you would weigh on that star. If stars had solid surfaces on which you could stand, then your weight would change from star to star. The new method allows scientists to measure surface gravity with an accuracy of about four percent, for stars too distant and too faint to apply current techniques. Since surface gravity depends on the star's mass and radius (just as your weight on Earth depends on its mass and radius), this technique will enable astronomers to better gauge the masses and sizes of distant stars. “If you don't know the star, you don't know the planet. The size of an exoplanet is measured relative to the size of its parent star,” said study co-author and professor Jaymie Matthews from University of British Columbia. If you find a planet around a star that you think is Sun-like but is actually a giant, you may have fooled yourself into thinking you've found a habitable Earth-sized world. “Our technique can tell you how big and bright is the star, and if a planet around it is the right size and temperature to have water oceans, and maybe life,” Matthews added. The new technique called the “autocorrelation function timescale technique” or timescale technique for short, uses subtle variations in the brightness of distant stars recorded by satellites like Canada's MOST and NASA's Kepler missions. Future space satellites will hunt for planets in the 'Goldilocks Zones' of their stars. Not too hot, not too cold, but just right for liquid water oceans and maybe life. Future exoplanet surveys will need the best possible information about the stars they search, if they're to correctly characterize any planets they find. “The timescale technique is a simple but powerful tool that can be applied to the data from these searches to help understand the nature of stars like our Sun and to help find other planets like our Earth,” explained lead author Thomas Kallinger from University of Vienna. It will play an exciting role in the study of planets beyond the Solar System, many so distant that even the basic properties of the stars they orbit can't be measured accurately. The new method is described in a study published in the journal Science Advances.	4.125	4	[ 0.015625, -0.00592041015625, 0.005584716796875, 0.0240478515625, -0.01611328125, -0.027099609375, -0.01226806640625, -0.006195068359375, 0.003631591796875, -0.04541015625, 0.01177978515625, 0.015869140625, -0.018310546875, 0.0028533935546875, -0.01611328125, 0.006561279296875, -0.01507568359375, -0.000446319580078125, 0.01470947265625, 0.01129150390625, 0.004180908203125, 0.00799560546875, -0.0079345703125, 0.00732421875, -0.009521484375, 0.007476806640625, 0.0086669921875, -0.0172119140625, 0.004608154296875, -0.01080322265625, 0.01544189453125, 0.012939453125, -0.01336669921875, -0.000021576881408691406, 0.01556396484375, 0.01312255859375, -0.00170135498046875, 0.007568359375, -0.0185546875, 0.0169677734375, 0.0166015625, -0.017822265625, -0.0093994140625, 0.0032196044921875, -0.017822265625, -0.000010251998901367188, -0.00701904296875, 0.006072998046875, 0.001922607421875, 0.010498046875, 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The inventive concept relates generally to electronic data storage technologies. More particularly, the inventive concept relates to data storage devices and related methods of operation. The information age has produced an explosive increase in the demand for personal data storage. With this increasing demand, various types of personal data storage devices have proliferated. For example, hard disk drives (HDDs) have been widely used due to various attractive features such as high recording density, high speed of data transmission, fast data access time, and low cost. Unfortunately, an HDD can be damaged by even slight shock and vibration due to its use of a platter and complex mechanical parts. In recent years, solid-state disks or drives (SSDs) have been developed to replace HDDs. An SSD is a data storage device that uses a solid-state semiconductor memory as a main form of data storage. Unlike HDDs, SSDs do not include a platter and related mechanical parts. As a result, SSDs tend to have lower mechanical driving time and latency, and faster read/write times compared with HDDs. They also tend to have fewer errors due to latency and mechanical friction compared with HDDs, so their reliability in performing read/write operations tends to be better than that of HDDs. Moreover, SSDs generate relatively little heat and noise during operation, and they can withstand physical shock, which makes them increasingly more attractive than HDDs. Due to the increasing popularity of SSDs, researchers are currently devoting great efforts to improving numerous aspects of their performance, including read/write speed, storage capacity, power consumption, reliability, durability, and many others.	3.34375	3	[ -0.003143310546875, 0.010009765625, 0.0019378662109375, -0.00128936767578125, -0.0194091796875, -0.0211181640625, -0.004638671875, -0.003814697265625, -0.01348876953125, 0.00811767578125, 0.00555419921875, 0.01611328125, -0.01055908203125, -0.005157470703125, -0.01055908203125, 0.007354736328125, -0.00946044921875, -0.00970458984375, -0.00970458984375, -0.00176239013671875, 0.0255126953125, -0.01031494140625, -0.01312255859375, 0.00151824951171875, -0.0040283203125, -0.0029144287109375, 0.007781982421875, 0.002227783203125, -0.00885009765625, 0.003204345703125, 0.0120849609375, 0.017578125, -0.0303955078125, 0.00347900390625, 0.018310546875, -0.01104736328125, 0.003570556640625, 0.0025177001953125, 0.014404296875, 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This invention relates to the identification and use of cis acting nucleic acid elements that bind to nucleic acid binding factors to regulate genetic activities of nucleic acids. All living creatures store information in nucleic acid molecules called DNA or RNA that encode structural and regulatory proteins. The collective behavior of nucleic acids and proteins constitutes and controls normal cell and organismal life cycles. Nucleic acids and proteins also act as causative agents in, or response factors to, pathological conditions. Transcription of DNA into RNA, translation of RNA into proteins and other genetic events such as nucleic acid synthesis, sorting, processing, repair and degradation, are regulated by a variety of specialized nucleic acid binding factors. Nucleic acid binding factors bind to specific sequences present on the nucleic acid molecules they regulate, called cis acting nucleic acid elements. These nucleic acid binding factors, bound to their specific cis acting nucleic acid elements, are able to interact with other cellular factors to modulate specific genetic events. The binding of a nucleic acid binding factor to a cis acting nucleic acid element, or its ability to interact with other factors that mediate genetic events, or both, can be regulated in response to signals transmitted into the cell from the cell exterior. As an example, regulatory proteins called xe2x80x9ctranscription factorsxe2x80x9d bind to cis acting nucleic acid elements on genomic DNA at sites known as xe2x80x9cpromotersxe2x80x9d and xe2x80x9cenhancersxe2x80x9d present at variable distances from the site of initiation of transcription of the genes they regulate. The enhancer sequences and adjacent nucleic acid sequences, together with their bound transcription factors, are able to bend to contact the transcriptional complex bound to the promoter. Such contact can either enhance or reduce expression of the regulated gene. The human genome, which stores the genetic information of a human cell as DNA, is estimated to contain about 100,000 genes. Each of these genes and the RNAs they encode is likely to have multiple cis acting nucleic acid elements that bind to corresponding nucleic acid binding factors to regulate gene expression. These cis acting nucleic acid elements, and the factors that bind them, are potential targets for therapeutic drugs that could be used to modulate gene expression. Determining which cis acting nucleic acid elements are bound under different conditions can also be used to characterize and monitor the genetic responses of a cell under normal, pathological or experimental conditions. Current methods of identifying cis acting nucleic acid elements have several disadvantages. Most of these methods require prior identification of either the nucleic acid that is regulated, or the corresponding regulatory nucleic acid binding factor, or both. For example, once a nucleic acid has been identified, adjacent sequences, which are predicted to contain cis acting nucleic acid elements, can be isolated and subsequences therefrom are tested for cis activities. Alternatively, once a nucleic acid binding factor has been isolated, the sequences to which it binds can be identified. Other methods, which are limited to identifying transcriptional enhancer elements, involve cloning random nucleic acid sequences upstream of a reporter gene and observing expression of the reporter gene product. At present, however, there is no broadly applicable method to identify cis acting nucleic acid elements without prior identification of the regulated nucleic acid or of the regulatory nucleic acid binding factor. There is also no rapid and efficient method to simultaneously identify a plurality of cis acting nucleic acid elements. Thus, there exists a need for a method of rapidly and efficiently identifying cis acting nucleic acid elements. The present invention satisfies this need and provides related advantages as well. The invention provides a method of identifying nucleic acids containing cis acting nucleic acid elements. The method consists of contacting a diverse population of nucleic acid binding factors with a diverse population of isolated nucleic acid molecules under conditions that allow the nucleic acid binding factors to selectively bind the nucleic acids. The nucleic acids that bind the nucleic acid binding factors are identified and are characterized as nucleic acids containing cis acting nucleic acid elements. The method simultaneously provides for the isolation of nucleic acid binding factors that selectively bind the isolated nucleic acid molecules. The invention also provides methods of identifying compounds that are cis acting nucleic acid element analogs, compounds that are nucleic acid binding factor analogs, and compounds that selectively bind cis acting nucleic acid elements. The invention further provides methods to identify compounds that selectively displace binding between a nucleic acid binding factor and a cis acting nucleic acid element or between nucleic acid binding factors. The invention further provides a plurality of isolated nucleic acid molecules that each contain one or more cis acting nucleic acid elements. Also provided is a plurality of isolated cis acting nucleic acid element analogs. The isolated nucleic acid molecules containing cis acting nucleic acid elements and the isolated cis acting nucleic acid element analogs in the pluralities can be bound to nucleic acid binding factors. A plurality of isolated nucleic acid binding factors is also provided. The invention also provides a method of determining a binding state of a nucleic acid. The method consists of contacting a nucleic acid with a plurality of isolated cis acting nucleic acid elements under conditions that allow nucleic acid binding factors bound to the nucleic acid to bind to the isolated cis acting nucleic acid elements. The isolated cis acting nucleic acid elements that bind the nucleic acid binding factors are identified and characterize the binding state of the nucleic acid. The invention further provides a method of treating a pathological condition in an individual. The method consists of administering to the individual an effective amount of a therapeutic agent that selectively alters the ability of a cis acting nucleic acid element to regulate a genetic activity of a nucleic acid involved in the pathological condition. Also provided is a method of treating a pathological condition in an individual by contacting a cell of the individual with an effective amount of a targeting construct that includes a cis acting nucleic acid element and targeting sequences. The targeting construct is taken up by the cell and inserted by homologous recombination into a nucleic acid involved in the pathological condition so as to alter a genetic activity of the nucleic acid.	3.046875	3	[ -0.017333984375, 0.0126953125, 0.01080322265625, -0.01287841796875, -0.01226806640625, 0.01519775390625, -0.010986328125, -0.007598876953125, -0.007171630859375, 0.0125732421875, 0.01116943359375, 0.005340576171875, -0.016845703125, 0.00946044921875, -0.01239013671875, -0.003753662109375, -0.005401611328125, 0.003814697265625, -0.0120849609375, -0.0047607421875, 0.04052734375, -0.009521484375, 0.0022125244140625, 0.003662109375, -0.0196533203125, 0.0057373046875, 0.00848388671875, 0.01348876953125, 0.0035247802734375, -0.004119873046875, 0.00823974609375, 0.0004596710205078125, -0.0167236328125, -0.010986328125, 0.006439208984375, -0.0057373046875, 0.0262451171875, -0.006256103515625, -0.00567626953125, -0.035400390625, -0.0052490234375, 0.000865936279296875, 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Click on the image above to download a moderately sized image in JPEG format (possibly reduced in size from original) Original Caption Released with Image: Context image All this week, the THEMIS Image of the Day has been following on the real Mars the path taken by fictional astronaut Mark Watney, stranded on the Red Planet in the book and movie, The Martian. Generally smooth and rolling terrain covers most of this portion of Schiaparelli Crater's floor. Because the impact that made Schiaparelli occurred billions of years ago, nature has had ample time to leave lava and sediments in the crater and to erode them. The ridge in the image's southern end is part of an eroded crater rim, one of many such smaller impact craters that have collected on Schiaparelli's floor since it formed. (This image was taken as part of a study for the Mars Student Imaging Project by a high-school science class.) Here astronaut Mark Watney's great overland trek reaches its end. He arrives safely at the Mars Ascent Vehicle (MAV), which was sent in advance for the next Mars mission crew. The rocket will get him off the ground and into Mars orbit, where he can be picked up by a rescue ship coming from Earth. NASA's Jet Propulsion Laboratory manages the 2001 Mars Odyssey mission for NASA's Science Mission Directorate, Washington, D.C. The Thermal Emission Imaging System (THEMIS) was developed by Arizona State University, Tempe, in collaboration with Raytheon Santa Barbara Remote Sensing. The THEMIS investigation is led by Dr. Philip Christensen at Arizona State University. Lockheed Martin Astronautics, Denver, is the prime contractor for the Odyssey project, and developed and built the orbiter. Mission operations are conducted jointly from Lockheed Martin and from JPL, a division of the California Institute of Technology in Pasadena.	3.046875	3	[ 0.009521484375, 0.02001953125, 0.00872802734375, 0.01312255859375, -0.00946044921875, -0.014892578125, -0.00787353515625, -0.017333984375, -0.0013275146484375, -0.000339508056640625, 0.0098876953125, -0.007232666015625, -0.029296875, 0.01953125, -0.005340576171875, 0.0115966796875, -0.01373291015625, 0.01043701171875, 0.0263671875, 0.0012969970703125, 0.011962890625, -0.0166015625, -0.006683349609375, 0.003204345703125, 0.004547119140625, 0.003662109375, -0.0142822265625, -0.037841796875, 0.01806640625, -0.000194549560546875, 0.0133056640625, -0.01385498046875, -0.0067138671875, -0.00604248046875, -0.0059814453125, 0.012939453125, -0.0228271484375, 0.003662109375, -0.01025390625, 0.00012493133544921875, -0.00653076171875, -0.0101318359375, -0.01007080078125, -0.01019287109375, 0.015380859375, -0.00250244140625, 0.000522613525390625, 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Q: How to deform a 2d shape to make a 3d object? I have a 2d flat mesh that i would like to manipulate without any distortion to create a 3D shape. Typically for the pie below, joining the 2 edges together would make a 3D cone. Do you have any idea of which modifier to use ? A: Using a script to make the two shape keys. Change the r and h of result cone. Example of radius 1, height 2, 1 and 0.5 cones. import bpy import bmesh from mathutils import Vector from math import radians, sin, cos, sqrt from bpy import context # for testing r = 1 # radius of cone h = 1 # height of cone sectors = 16 l = sqrt(r2 + h2) # hypotenuse # sector will have angle theta = radians(360) * r / l dtheta = theta / sectors # build the base bm = bmesh.new() verts = [] for i in range(sectors + 1): a = i * dtheta verts.append(bm.verts.new((l * cos(a), l * sin(a), 0))) topvert = bm.verts.new((0, 0, 0)) for i in range(sectors): bm.faces.new([verts[i + 1], topvert, verts[i]]) cone_mesh = bpy.data.meshes.new("Cone") cone = bpy.data.objects.new("Cone", cone_mesh) bm.to_mesh(cone_mesh) # add base as basis shape key basis_shape_key = cone.shape_key_add("Basis") # add second shape key cone_shape_key = cone.shape_key_add("Cone") offset = (radians(360) - theta) / 2 dtheta = radians(360) / sectors for v in verts: a = v.index * dtheta - offset cone_shape_key.data[v.index].co = ((r * cos(a), r * sin(a), 0)) cone_shape_key.data[topvert.index].co = (0, 0, h) # link to scene scene = context.scene scene.objects.link(cone) scene.objects.active = cone cone.select = True A: Managed to approximate this with Shape Keys, starting out with a cone, it's easier than starting out with a flat shape and bending it into your will. Add a cone mesh with whatever final dimensions you want it to have Move it in edit mode so it's center is on the center of the base (not mid height) Erase the left part and the bottom face and then add a Mirror modifier Add two new shape keys one is the base as it currently is, and another (Key 1) will be it's flat shape. Now some math, in edit mode check the length of one of the cone large side edges with the 3D view > Properties Region > Mesh Display > Length that will determine the radius of the final flat shape Add a new mesh circle object, it's radius should be the length of the previously measured edge, and it the number radius vertices should be 1 1/4 the number of vertices of the cone. So if by default a cone has 32 vertex so the circle should have 1.25 x 32 = 40 vertices. Erase one quarter of the circle's edges so that they are centered around the edge you ripped in Step 3 Now with shape Key 1 selected enter edit mode on the cone, move the central vertex down until it is flat Scale all the vertex in the cone base so that they reach the circle radius (use snap for better precision) Press .(Period Key) to transform centered in 3D Cursor Hide all the cone vertex but the outer rim of the base, including the vertex at X=0 With Proportional Edit set to Connected and the Fallof type set to Linear, select only the lower vertex and rotate them all 1/8 of a turn, so they snap to the open end of the circle. Adjust the Proportional Edit radius with the mouse wheel. 13.Profit! 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Pelican Island National Wildlife Refuge Pelican Island National Wildlife Refuge is a United States National Wildlife Refuge (NWR), and part of the Everglades Headwaters NWR complex, located just off the western coast of Orchid Island in the Indian River Lagoon east of Sebastian, Florida. The refuge consists of a island that includes an additional of surrounding water and is located off the east coast of Florida of the Indian River Lagoon. Established by an executive order of President Theodore Roosevelt on March 14, 1903, Pelican Island was the first National wildlife refuge in the United States. It was created to protect egrets and other birds from extinction through plume hunting. Management Pelican Island is administered as part of the Everglades Headwaters NWR complex along with Archie Carr NWR, Lake Wales Ridge NWR, and the Everglades Headwaters NWR and Conservation Area, created in 2012 (556th unit of the National Wildlife Refuge System) with a donation and other lands covering approximately north of Lake Okeechobee. will be held under "conservation easement"s through the U.S. Department of the Interior and the U.S. Fish and Wildlife Service. This allows landowners the right to retain ownership of the land, with the ability to continue farming or ranching, ensuring that the land can't be subdivided or developed. Pelican Island NWR has been placed on the List of Ramsar wetlands of international importance along with other areas of wetlands in the United States. Early history Pelican Island's bird populations were threatened because of increased American settlement around the area in the mid-19th century. Many of the exotic birds were killed for their feathers, used in the fashion industry. Plumes from the birds were used to adorn ladies' hats of the day and at the time were worth more than their weight in gold. Paul Kroegel, a German immigrant, moved to Florida in 1881 and lived on the west bank of Indian River Lagoon. He was fascinated with the pelicans on the island. Being able to see the island from his home, Paul would watch the pelicans and other water birds. He eventually took an interest in the island and its protection. However, there was not any state or federal law to help him so he took control of the situation himself. Kroegel sailed to the island to stand guard and protect the birds and the island. A few naturalists visited Kroegel at Pelican Island. A curator at the American Museum of Natural History in New York, Frank Chapman, was one of the naturalists showing interest in the island as well. He discovered that Pelican Island was one of the last rookeries of Brown pelicans on the eastern coast of Florida. The American Ornithologists' Union and the Florida Audubon Society led a campaign to pass legislation for protection of non-game birds in 1901. Knowing that the protection of Pelican Island would require more legislation, Chapman and his fellow advocate, William Dutcher went to President Theodore Roosevelt at his home in New York. The two appealed their case to Roosevelt's conservative ethics. President Roosevelt signed an executive order that established Pelican Island as the first federal bird reservation. This was the first time that the federal government put land aside for the sake of wildlife. The area, however, was open for big game hunters. Recent threats During the 1960s, Pelican Island was threatened by attempts to sell the surrounding wetlands and islands to developers. Local citizens led a fight to protect Pelican Island by stopping the sale of the wetlands. The Indian River Area Preservation League, formed by local citrus growers, commercial fishermen, and sportsmen, joined with Florida Audubon Society to convince the State to include the islands as a part of the refuge. "Later in 1963, Pelican Island was designated as a National Historic Landmark by the Secretary of the Interior because of its status as the first federal area set aside specifically to protect wildlife." In 1968, Florida agreed to expand to include nearly 5000 acres (20 km²) of mangrove islands and other submerged lands. And then in 1970, Pelican Island became the smallest wilderness area in the National Wilderness Preservation System. Since, the refuge has gained over 500 acres (2 km²) through purchases, management agreements, and conservation easements to provide a buffer against encroaching development and also to be a link to the Archie Carr National Wildlife Refuge. Pelican Island National Wildlife Refuge was added to the list of wetlands of international importance under the Ramsar Convention signed in 1971. Today, Pelican Island is also threatened by shoreline development. Shoreline development has many negative impacts associated with it. Shoreline development can reduce the water quality by increasing the runoff of sediments, fertilizers, and pesticides. These runoffs will cause decline in water quality, and this can directly affect the food base that sustains the island's nesting bird colonies. Waterfront development will also lead to more boat traffic. This extra boat traffic will also negatively affect the birds on the coast. Not only this, development of the shorelines of Pelican Island will permanently flaw the pristine character of this unique National Historic Landmark. Physical environment The environment of Pelican Island consists of climate, topography, geology, air quality, and waterways. Climate The climate at Pelican Island NWR is subtropical and temperate and experiences an average temperate of . Pelican Island has long, warm, and humid summers and short, mild winters and has an average rainfall of about annually. Pelican Island may experience tropical storms in the period from May to November. Topography The elevation of Pelican Island changes from east to west. It rises sharply from sea level to about and then drops back down more slowly to below sea level in the Indian River Lagoon. The land between the Indian River Lagoon and St. Sebastian River is . Even further west, there is an ancient dune that rises in elevation from to . Geology The landscape of Pelican Island area is made of Pleistocene (glacial) and Holocene (recent) origin. Submerged lands were exposed during the late Pleistocene period, allowing for the spread of flora and fauna from the peninsula. Wetlands, salt marshes, mangroves, and other swampy formations make up the uplands and submerged lands. Soil "The general soils in the Pelican Island Refuge are Canaveral-Captiva-Palm Beach, which is characterized by the gently sloping, somewhat poorly drained to moderately drained sandy soils with shell fragments, and McKee-Quartzipsamments-St. Augustine, which is characterized by level, somewhat poorly drained soils mixed with sand and shell fragments." Other soils include Canaveral Fine Sand, Quartzipsamments, Captiva Fine Sand, McKee Mucky Clay Loam, and Kesson Muck. Air quality Good air quality is vital for the refuge to maintain itself. A few problems dealing with air pollution are carbon monoxide, lead, nitrogen dioxide, ozone, particulate matter, and sulfur dioxide. The primary producers of these pollutants are vehicle emissions, power plants, and industrial activities. The Indian River Lagoon area is said to have good air quality. Sometimes occasional temperate increases can temporarily degrade the air quality below the accepted levels. Waterways The Indian River Lagoon stretches from Ponce de Leon south of Daytona Beach to Jupiter Inlet near West Palm Beach, a distance of about , and contains a number of small rivers, creeks, and canals. The Intracoastal Waterway is the deepest part of the Lagoon. St. Sebastian River and Turkey Creek provide freshwater to the Lagoon. Water quality is also a concern in the refuge: cadmium, lead, mercury, nutrients, selenium, thallium, and dissolved oxygen. The water circulation is affected by the Intracoastal Waterway, winds, inlets, and causeways. Within the refuge boundary, the water quality is generally better compared to portions of the Lagoon. Wildlife Pelican Island National Wildlife Refuge holds hundreds of species of animals including birds, fish, plants, and mammals. The wetlands of Pelican Island are a major ecological system supporting the huge biological diversity. Fifteen federally listed threatened and endangered species live in Pelican Island NWR and around Indian River Lagoon. Of the endangered species, West Indian manatees and sea turtles occupy parts of the lagoon. Around the lagoon in the refuge are two wood stork refuges. These birds along with other wading birds that nest on the island thrive on the tremendous fish population. Pelican Island is home to many nesting birds including brown pelicans, great egrets, snowy egrets, reddish egrets, great blue heron, little blue heron, tricolored heron, black-crowned night heron, American white ibis, glossy ibis, double-crested cormorant, anhinga, and American oystercatcher. Visiting Pelican Island is only accessible by boat or chartered tours. Nesting birds are easily disturbed, so people are not allowed to get too close or to disembark. Visiting during nesting season (late November through late July), one can expect to see brown pelican, wood storks, white ibises, black-crowned night herons, double-crested cormorants, reddish, snowy, and great egrets, and great blue, little blue and tricolored herons. Traveling in the winter, look for lesser scaup, blue-winged teal, mottled ducks, great northern divers, laughing gulls, American white pelicans, and red-breasted mergansers. Summer visitors should watch for roseate spoonbills, magnificent frigatebirds and least terns. Pelican Island also features some marine life in the Indian River including sea turtles, dolphins, and manatees. New public facilities were opened and dedicated on March 14, 2003, in ceremonies marking the centennial of Pelican Island and the National Wildlife Refuge System. A 37¢ US Commemorative Stamp in honor of the NWR Centennial was issued as part of the celebration. The new facilities include a 1/4 mile boardwalk and observation tower to view Pelican Island, two salt marsh impoundment foot trails, interpretive signs, informational kiosks, restrooms and parking areas. The facilities are west of Highway A1A on the north end of Historic Jungle Trail. They were produced through a partnership with Indian River County, St. Johns River Water Management District, Florida Inland Navigation District, Florida Power and Light, ConocoPhillips, Wild Birds Unlimited, the National Fish and Wildlife Foundation, and many others. Future plans include additional boardwalks, an overlook, a photo blind and a wildlife drive. Budget cuts Pelican Island, along with many other wildlife refuges, has been experiencing budget cuts. Many problems arise from the stagnant budget and lack of maintenance in the wildlife refuges. These are vital to preserve the habitat and the wildlife and to provide public education and recreation. This situation worsened further because of the failure of congress to timely pass federal funding bills. Staffing at Pelican Island is made up of U.S. Fish and Wildlife Service. The staff members have recently fallen from six to two which has had many negative consequences. The cuts have led to limiting refuge work and restricting public visitation. Another consequence is the end of 14-year tradition of the wildlife festival. Pelican Island will be losing its only public-use staff and eliminating all active outreach at the nation's first wildlife refuge. Pelican Island Refuge manager and project leader Paul Tritaik said in 2006 that reductions to a full-time staff would lead to the end of some refuge activities and the loss of several trails. See also Florida State Parks Indian River County, Florida List of National Wildlife Refuges History of the National Wildlife Refuge System Notes References Dinnage, Russell J. "WILDLIFE REFUGES: Budgetary downturn for national refuges hits staffers hardest." Land Letter. 16 November 2006. Hem, Brad. "Looking ahead, Pelican Island may be next in line: Port of Houston buys land, could join Galveston in a joint effort." The Houston Chronicle. 4 February 2007. McHugh, Paul. "Wildlife refuges on life support; Flat budgets imperil future of the system." The San Francisco Chronicle. 21 December 2006. "Parks: Pelican Island National Wildlife Refuge." GORP. 2007. 26 April 2007. <http://www.gorp.com/parks-guide/travel-ta-prime-hook-national-wildlife-refuge-pelican-island-national-wildlife-refuge-birdwatching-sidwcmdev_068511.html>. "Pelican Island National Wildlife Refuge: Comprehensive Conservation Plan." U.S. Fish and Wildlife Service. Sept 2006. 9 May 2007. <http://library.fws.gov/CCPs/pelicanisland_final.pdf>. "Pelican Island National Wildlife Refuge." U.S. Fish and Wildlife Service. 2007. 26 April 2007. <http://www.fws.gov/pelicanisland/>. 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Children enjoy toys that can captivate their attention. A toy ball is a particular play item that has endured the test of time and remained a favorite with children of all ages (infants, toddlers, etc.). However, as with any child's toy, some intrinsic dangers must be avoided. According to the U.S. Consumer Product Safety Commission, small objects can easily be lodged in the airway of young children, creating a choking hazard. Thus, it is imperative to create toy balls that are increasingly safe for use by children. Furthermore, a toy ball is often constructed from more than one base component (e.g., two half-spherical (hemispherical) shells that may be attached together to form a substantially spherical shell) in order to form a spherical structure. If these components that are used to construct the toy balls also contain small parts, they may create additional choking hazards to children in the event they come free during use. Thus, the particular construction of the components making up the toy ball must be considered so as to ensure safe use by children. In addition, ancillary entertainment features are often incorporated into toy balls (e.g., figurines, rattling elements, fluids, etc.) in order to further captivate and hold a child's attention. Such ancillary features are intended to be stimulating and aesthetically pleasing so as to maintain the attention span of most children. It should be noted, however, that some of these ancillary entertainment features may be sufficiently small in size so as to pose a potential choking hazard to children. Children sometimes play in rough manner. Thus, toys should generally be constructed so as to minimize the risk of damage during the normal course of play. In the instant case, a toy ball is sometimes subjected to rough play. A toy ball is subject to a plethora of physical activities (e.g., being thrown, rolled, dropped, hit, batted, etc.). Should a toy ball be broken apart in the course of play, the contents within the ball would be exposed/set free and, as such, the freed contents may constitute a risk to the safety of children playing with the toy. Additionally, the broken toy would be rendered unfit for future use. Prior art toy balls typically are constructed from two shell halves mated together to form a seam along an equator of the toy ball. Such prior art toy balls are illustrated in U.S. Design Pat. No. 274,070 to Ma, U.S. Design Pat. No. 190,036 to Lakin, U.S. Design Pat. No. 314,598 to Capper et al. (illustrated in FIG. 1), U.S. Pat. No. 4,272,911 to Strauss, U.S. Pat. No. 2,519,248 to Hulbert, and U.S. Pat. No. 2,351,762 to Hoover. The method of affixing one shell half to another can include but are not limited to cementing, heat-sealing, ultrasonic welding, and dielectric welding. Still other toys have a substantially formed sphere, with an opening to insert an additional entertainment item, and are then capped to encapsulate the item within the sphere. An example of such a prior art toy ball is illustrated in U.S. Pat. No. 4,601,675 to Robinson. During rough play, the toy balls have an increased risk of breaking open. The toy balls found in the prior art are not inherently resistant to forces acting perpendicular to the seam running along the ball's equator. More specifically, the equatorial seam provides little resistance to a shearing force applied at the seam or to tensile forces acting on the two shells perpendicular to the seam. Thus, it would be desirable to provide toy balls with a greater factor of safety for children. In particular, it would be desirable to provide a toy ball that possesses additional strength to withstand shearing forces acting on the seam of the toy ball. Additionally, it would be desirable to provide a toy ball that possesses additional strength to withstand tensile forces acting on the two shells perpendicular to the seam. Such additional strength would enhance the intrinsic value of a toy by providing an additional level of safety for children. Furthermore, while the addition of an element to structurally strengthen the toy ball is desired, any such element should not detract from the aesthetically pleasing nature of the toy ball to a child. Thus, there exists a need for providing a toy ball that has a construction that adds strength to the ball's seam in order to prevent the toy ball from breaking open and exposing its contents to the child playing with the ball. Furthermore, any additional element incorporated into the construction of the toy ball should be generally aesthetically pleasing to a child. Providing such an arrangement that both increases the toy's safety and makes the toy more aesthetically desirable not only increases a child's enjoyment, but also increases the attractiveness of the toy to anyone concerned with the safety of children. This invention is directed generally to a toy ball with additional strength to resist forces in a tensile direction or shearing forces applied to a main seam. More specifically, this invention is directed to a toy ball having two shells (hemispherical or unequal in size) fused together forming a seam, the toy ball also having opposing end caps, each end cap capturing a portion of each shell to resist both shearing and tensile forces acting on the seam.	3.046875	3	[ 0.0052490234375, 0.000812530517578125, -0.004638671875, -0.00025177001953125, -0.0311279296875, -0.01141357421875, 0.01190185546875, 0.00494384765625, -0.002197265625, -0.0045166015625, 0.0098876953125, 0.004669189453125, 0.0133056640625, -0.0021514892578125, -0.005828857421875, 0.00811767578125, 0.017333984375, -0.004058837890625, 0.0028839111328125, 0.00091552734375, 0.058349609375, 0.01556396484375, -0.015380859375, -0.01904296875, -0.002410888671875, -0.002197265625, 0.00341796875, -0.0015411376953125, 0.0086669921875, -0.000457763671875, -0.00012969970703125, 0.0126953125, -0.0196533203125, 0.00064849853515625, 0.00750732421875, -0.00482177734375, 0.015625, 0.003448486328125, 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Chapter 17 Chapter 17 Chapter 17 Chapter 17 Chapter 17 Chapter 17 Summary Grief, Didion tells us, is never quite what we expect. Though we know that the people close to us will die, we don’t look beyond the days or weeks immediately following their deaths. We expect to be crazy and inconsolable, but we don’t imagine that we will be “literally crazy,” as Didion terms it, believing that we have the power to bring a lost loved one back. We expect that the funeral will be the greatest test of our strength, when in fact the funeral is soothing, thanks to the comfort of others and the meaningful nature of the event. The test comes in the weeks and months following, when the mourning person must face a profound loneliness and sense of meaninglessness, and must do so alone. As a child, Didion had been fearful of the idea of meaninglessness and found comfort in geology. The shifting and changing patterns of the earth seemed inevitable and permanent, a notion Didion linked to the Episcopal saying, “As it was in the beginning, is now and ever shall be, world without end.” For Didion, the earth’s abiding indifference was a comfort. While the destruction of human life might cause personal sorrow, the world would always continue. After she married and had a child, Didion found further comfort in domestic routines, such as cooking meals and setting the table. People dealing with grief think a great deal about self-pity, Didion asserts. Self- pity, though common, is a practice almost universally condemned by society. Didion had spent nearly all of her time with John after they married, and her frequent impulse to talk to him didn’t go away after he died. With no one to share her thoughts with, she turns into herself, and that intense self-focus leads naturally to self-pity. Though some people who have experienced loss claim to feel the presence of the deceased, Didion never does. On several occasions after John dies, she speaks to him as if he were there, but she knows that, as a writer, imagining their dialogue comes naturally to her. However, as she imagines the responses he might give to her questions, Didion realizes that, while she thought she knew all of John’s thoughts, she really only knew a fraction of them. Before his death, John frequently told her that if something happened to him she should stay in their apartment, keep her friends close, and marry again within the year. But neither John nor Didion really understood the implications of John’s command, as both were incapable of imagining life without the other. Didion says “marriage is time,” referring to the significance of their shared history. It is also, she says, “the denial of time,” because since she was twenty-nine Didion had always seen herself through John’s eyes. Now she must see herself through other people’s eyes, and it makes her feel considerably older. In death, she says, we mourn not only the loss of the loved one but also the loss of ourselves. Analysis Didion has begun to take stock of the past year and now attempts to understand and draw a set of coherent conclusions from her experiences. She realizes that the intensity of the shock she felt at John’s death and her subsequent deranged reactions were not only caused by the suddenness of her intense loss, but also because she was jarred to realize that her expectations about grief had been so misguided. On the surface, she had been able to function without breaking down or becoming hysterical. In reality, she had temporarily been mentally ill, able to press on only because she deluded herself into thinking that she could bring John back. Didion had not only been shocked by grief, but also by her reaction to her own grief. In dealing with John’s absence, Didion realizes how much she communicated with him on a daily basis and how all that energy has now been turned inward. This intense level of self-focus might also be called self-pity, she worries. However, this powerful self-concern is an inevitable consequence of losing someone with whom she shared such a strong, unique bond. Didion is not only coping with the loss of John, but also with the loss of their shared memory. Her sense of self had been largely founded on her relationship—not because she lacked a strong identity of her own, but because their emotional, intellectual, creative, social, domestic, and daily lives were so bound together. The loss of John forces Didion to evaluate who she is without him, a daunting task, since she has not thought of herself in that way for forty years. Didion’s general reluctance to engage in behavior she deems indulgent makes her attempt to understand herself as an individual separate from John feel like an act of “self-pity,” but it is a necessary part of the healing process. When Didion discusses meaninglessness, she isn’t talking about an absence of meaning. Instead, she describes a way of looking at the world with a proper sense of perspective, acknowledging that personal tragedy seems insignificant when compared to massive geological shifts. Changes that can seem huge or overwhelming seem small when viewed within a broader perspective. Didion recalls how the indifference of the natural world served as a comfort to Didion as a child. This might seem like a strange concept, since many people find comfort in exactly the opposite notion: that there is, in fact, a higher consciousness that cares about our personal welfare and benevolently controls our individual lives. However, Didion’s childhood worldview still has religious overtones, as she takes comfort in the idea that the world exists on such a huge scale that she, as a single human being, could never fully comprehend it entirely. For someone who always needs to be right and who fervently believes that research can answer all questions, acknowledging that there are things in the world that cannot be fathomed or understood, even through the most diligent inquisition, is a profound shift in thinking and an important step toward ending the process of magical thinking.	3.046875	3	[ -0.006683349609375, 0.0059814453125, 0.004119873046875, 0.020263671875, -0.021728515625, -0.00421142578125, -0.0103759765625, -0.0023956298828125, -0.0177001953125, -0.01385498046875, 0.0052490234375, 0.00933837890625, -0.0223388671875, 0.0174560546875, -0.0079345703125, 0.0091552734375, 0.000354766845703125, -0.011962890625, -0.01202392578125, 0.005584716796875, 0.03515625, 0.004058837890625, -0.00714111328125, 0.0096435546875, -0.002777099609375, -0.00128173828125, 0.000644683837890625, -0.006591796875, 0.0133056640625, -0.0123291015625, -0.02294921875, 0.0072021484375, -0.025390625, -0.0162353515625, 0.01708984375, -0.0042724609375, 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How to Help Language Impaired Students Improve their Leisure Skills Do you have students on your caseload who have very limited leisure skill interests? Are these students often left out of group activities at school and in the home environment? When our students do not engage in play/ leisure activities they are missing out on a natural way to work on language instruction. Read the following article, a guest post by Rosemarie Griffin from ABA Speech, to help your students increase their functional language and leisure skills: Leisure skills can be addressed in a variety of ways in clinic or school based settings. If you have a student who receives direct individual therapy, you could work on a specific leisure skill during therapy and generalize it to a larger group, when the student is able to engage in the skill with minimal prompts from an adult. Another way to target leisure skill instruction would be to teach a specific leisure skill (i.e. modified musical chairs) to a small group of students. It is important whether you are teaching the skill in an individual or small group session that the students know exactly how to engage in the skill. There are many evidenced based strategies, but we will focus on the skill of video modeling. Video modeling is a mode of teaching that uses video recording. The video recording acts as a visual model of the targeted skill or behavior. It can take many forms. The video can be of the student engaging in the skill or it can be of another individual engaging in the skill. The learner watches the video and then they perform the skill in the moment or at a later time. For example, if you are teaching students to play UNO® as a modified game; you could make a video of students playing this game the modified way ( i.e. matching just the color cards or playing minus the skip, reverse, wild and draw two). You would show the video to the students learning the game and then have them play the game. There is a lot of research that supports using this strategy to teach skills to individuals with autism and other disabilities. Below I will describe 2 modified leisure activities that I use with my middle school and high school students. A favorite of game of my students happens to be UNO®. There are 2 ways to modify UNO® based on the level of learner you have in your group. For early learners, you can lay out one card of each color on the table ( yellow, red, green, blue) and put the other cards face down. You each take a turn picking a card and matching it to the cards on the table. If your students are ready for more of a challenge you can play uno the regular way but without the skip, reverse, wild and draw two cards. This is such a popular game and one that many families have at home. It would be great to work on this at school and let the parents know about all of the work that you have done. Playing UNO® at home would be a wonderful way for your student to spend quality time with his family, while generalizing this leisure skill to new people and new environments. Another game that many of my students enjoy is playing Scrabble®. We each pick seven tiles and take turns making words on the board. The modification is that the words do not have to be connected in any way. This is what makes Scrabble® so difficult! I allow the students to make a word anywhere that they want on the board. If you have a student in the group who is having difficulty making a word on their own, grab a dry erase board and write down a word for them that they could make with their tiles. They can pick the tiles and match them to the word and transfer to the board. Viola a wonderful way to enjoy a cooperative group activity with students of varying ability levels. Being able to participate in age appropriate leisure skills gives students the opportunity to practice social language skills and helps them to feel more included with peers and their family members. Working on leisure skills can be enjoyable for all; I hope that these strategies will help you incorporate this instruction into your therapeutic practice. Rosemarie Griffin is a speech language pathologist, board certified behavior analyst and product developer. She is the creator of the Action Builder Cards. To learn more about modified leisure skills or to gather information about using applied behavior analysis to help students increase their communication skills, check out her website www.abaspeech.org or like her Facebook page here: ABA SPEECH ON FACEBOOK. Ms. Gardenia on Instagram Notice This website or its third-party tools use cookies, which are necessary to its functioning and required to achieve the purposes illustrated in the cookie policy. If you want to know more or withdraw your consent to all or some of the cookies, please refer to the Cookie Policy. By closing this banner, scrolling this page, clicking a link or continuing to browse otherwise, you agree to the use of cookies. By using our site, you acknowledge that you have read and understand our Cookie Policy, Privacy Policy, and our Terms of Service. 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The regulations allow approximately 11.7 million instances of harassment, injury, or even death (the legal term is "take") to marine mammals by exposing them to high-intensity military sonar training in coastal waters around the United States. These estimates – the Navy's own – include 9.7 million takes along the Atlantic Coast and the Gulf of Mexico; 630,000 off the coast of southern California; 650,000 along the coast of Washington and Oregon; 140,000 in Hawaii; and another 500,000 off the coast of Florida. Sonar exposure is not, as the Navy suggests, a mere matter of annoyance to whales and dolphins. In fact, the harm ranges from significant disturbance to important behaviors – feeding, breeding, migrating, communicating, finding mates – to hearing damage and even mass stranding and death. At risk are not only some of the most vulnerable whale populations on Earth – including the last remaining 300 North Atlantic right whales and the 83 critically endangered southern resident killer whales off the Washington coast – but the very fabric of life among species that, over eons in the dark ocean, have evolved to depend on sound as we depend on sight. According to government scientists, the "loss of even a single individual right whale may contribute to the extinction of the species." In recent decades, a growing number of mass whale mortalities around the world have occurred in the shadow of military sonar training, in coastal waters as diverse as the Bahamas, the Canary Islands, Greece, North Carolina, Hawaii, Washington State, and many others. According to scientists – including the Navy's own consultants – there is no longer any doubt that sonar kills whales, whether by stranding or massive internal hemorrhaging – akin to what human divers experience as the "bends." Nor, as the Navy has argued, is sonar's impact a necessary consequence of securing our national defense. Most of the harm to marine mammals authorized by the Bush administration could be avoided by the use of common sense safeguards, many of which the Navy has used in past training exercises without apparent problem. Simple steps such as avoiding sensitive areas like marine sanctuaries, critical habitats, and feeding or breeding grounds; adopting adequate monitoring and safety zones around the sonar device; powering down in ocean conditions of particular acoustic risk; and implementing ship based, aerial, and underwater techniques to monitor when marine mammals are present enable a protective response. But for all of the recent proposed sonar training, the Navy has refused to implement any of this mitigation, instead proposing half-measures dismissed by the federal courts as "woefully inadequate and ineffectual." During the past decade, the courts have been the only effective line of defense against the Navy's needlessly dangerous sonar training, but litigation is piecemeal. A more effective, more comprehensive political response may now be possible. And given the geographic reach of the proposed sonar training and the Navy's own predictions of harm, such a response may be the only way to counter what amounts to an astonishing acoustic assault on marine life along all our coasts. New leadership is already in place at NOAA. New leadership, we hope, will soon be coming to the US Navy. Instead of the Bush administration's last-minute attack on whales and other marine life, the new administration should require a uniform protocol of effective safeguards for all Navy sonar training that would prevent the needless infliction of harm. We urge NOAA to move quickly and forcefully to exercise its authority – and fulfill its responsibility – to protect our oceans.	3.015625	3	[ 0.012939453125, -0.0081787109375, 0.0024261474609375, 0.00970458984375, -0.0147705078125, 0.000926971435546875, -0.0177001953125, 0.01507568359375, -0.00244140625, 0.01953125, 0.0020599365234375, 0.004913330078125, 0.0068359375, -0.00909423828125, -0.004425048828125, 0.007049560546875, -0.005584716796875, 0.006500244140625, 0.0185546875, -0.00128173828125, 0.0169677734375, -0.0157470703125, -0.01263427734375, 0.0181884765625, -0.000518798828125, -0.0133056640625, -0.0037078857421875, -0.0169677734375, 0.0247802734375, -0.00653076171875, 0.0010986328125, 0.01300048828125, -0.0267333984375, -0.0130615234375, 0.006500244140625, -0.00160980224609375, 0.0157470703125, 0.01446533203125, -0.00994873046875, 0.01153564453125, 0.00022029876708984375, 0.007080078125, 0.000255584716796875, -0.0018768310546875, 0.001495361328125, 0.0031890869140625, 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Epidemiology, Genetic Recombination, and Pathogenesis of Coronaviruses. Human coronaviruses (HCoVs) were first described in the 1960s for patients with the common cold. Since then, more HCoVs have been discovered, including those that cause severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome (MERS), two pathogens that, upon infection, can cause fatal respiratory disease in humans. It was recently discovered that dromedary camels in Saudi Arabia harbor three different HCoV species, including a dominant MERS HCoV lineage that was responsible for the outbreaks in the Middle East and South Korea during 2015. In this review we aim to compare and contrast the different HCoVs with regard to epidemiology and pathogenesis, in addition to the virus evolution and recombination events which have, on occasion, resulted in outbreaks amongst humans.	3.015625	3	[ -0.0037689208984375, 0.01507568359375, 0.03466796875, 0.0045166015625, -0.00927734375, 0.00110626220703125, 0.0101318359375, -0.0206298828125, 0.00173187255859375, -0.019775390625, 0.004913330078125, -0.0125732421875, -0.0269775390625, 0.002655029296875, -0.005401611328125, -0.0123291015625, 0.00439453125, -0.000591278076171875, -0.0164794921875, -0.0004730224609375, -0.0045166015625, -0.0023193359375, -0.001617431640625, -0.0032196044921875, 0.017333984375, 0.00946044921875, -0.00372314453125, -0.0162353515625, -0.000537872314453125, -0.003997802734375, -0.0128173828125, 0.01422119140625, -0.0245361328125, -0.0284423828125, -0.00003814697265625, -0.00958251953125, 0.0147705078125, -0.004547119140625, -0.0068359375, 0.009033203125, 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Opaque, white steam trailing behind loud trucks were a routine sight in many a childhood around the world. In South Korea, too, trucks would wail out siren sounds while emitting disinfectants and children would chase after the trucks through narrow alleyways, breathing in the foul-smelling gas. Used as a pesticide against mosquitoes and larvae, as well as a general means to prevent infectious disease, these disinfectants have remained a regular part of national public health measures since the mid-1900s. But within the past decade, these trucks have become increasingly difficult to catch in the streets of South Korea. A video posted by a South Korean user, chasing after a disinfecting truck (Source: YouTube) Traditional smoke disinfectant is effective in its ability to rapidly disinfect large areas. And its explicitly loud, smoke-spewing nature does more than give young children something fun to do — according to the Gwangjin-gu Public Health Center in Seoul, one of its advantages is that “its visible nature leads to citizen support.” But smoke disinfectant — made by diluting kerosene or heavy oil with insecticide and sprayed with a heater — affects an unpredictable radius. This can lead to unexpected health risks to residents in nearby housing areas, according to a 2015 Ministry report from the Ministry of Health and Welfare. Smoke disinfectants include chemicals dangerous to the environment. For example, when oils are not completely combusted, the resulting solution contains volatile compounds such as belen, toluene and other carcinogens that can be harmful to both people and the environment. Just last year, Busan, South Korea’s second largest city with a population of three million, announced efforts to increase environmentally friendly solutions with an investment of 500 million won, according to daily newspaper Busan Ilbo. While the traditional disinfectant is still necessary for hard-to-access areas such as sewers, the ultimate goal is to reduce the use of smoke disinfectant from 72 to 25 percent. Citizens and governmental agencies have become more cognizant of potential dangers, calling either for a ban or changes to trucks spraying disinfectant gases. The Ministry of Health and Welfare said that it recommends, instead of excessive smoke disinfectant, spray methods or targeting larvae before they develop. With new technologies and increased health concerns, the nostalgia-inducing images of smoke trailing behind a blaring truck are surely becoming much more of a rarity. But that doesn’t mean they’ve stopped entirely, nor will they any time soon. In 2005, daily newspaper Hanykoreh reported that of 246 public health centers across the country, 239 — practically all of them — were using smoke disinfectant. Seven years later, Hankoyreh conducted another similar study (although this time with far fewer centers) and found that 23 out of 36 public health centers contacted across the country still planned to use smoke disinfectant. Though the traditional oil-based smoke disinfectants are far from extinct, many of the centers in the recent study are showing efforts, such as water-based solutions, to become more environmentally friendly. And as public health centers seek out new, safer mixtures, in response to rising public awareness about the possible dangers of these trucks, health measures are shifting — from what was once an explicit, loud display of communal cleaning into a humbler national effort to do the same job but maybe in a safer way. Cover image: Though less common now, mosquito trucks spewing disinfectant smoke have long been a common sight in South Korea. 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Wouldn't it be great if, when landing a robotic mission on another planet, the lander or rover could just scoop a sample, drop it into a chemical analyzer and get a "positive" or "negative" result for extraterrestrial life? Well, this chemistry test isn't so far fetched and scientists at NASA's Jet Propulsion Laboratory in Pasadena, Calif., are working on a method that is 10,000 times more sensitive than any other method currently employed by spacecraft. Focused on the detection of specific types of amino acid tied to life, the researchers propose mixing a liquid sample collected from the surface of an alien world with a chemical known as a liquid reagent. Then, by shining a laser across the mixture, the molecules it contains can be observed moving at different speeds when exposed to an electric field. From this, the different molecules can be identified and the whole thing can be done autonomously, no humans required. The method known as "capillary electrophoresis" can be used to detect many different types of amino acids simultaneously. "Our method improves on previous attempts by increasing the number of amino acids that can be detected in a single run," said researcher Jessica Creamer in a statement. "Additionally, it allows us to detect these amino acids at very low concentrations, even in highly salty samples, with a very simple 'mix and analyze' process." RELATED: Stormy Alien Atmospheres May Spark Seeds of Life The team has already tested the method on water taken from Mono Lake in California - a mass of salty water with an extreme alkalinity - and simultaneously analyzed 17 different amino acids. "Using our method, we are able to tell the difference between amino acids that come from non-living sources like meteorites versus amino acids that come from living organisms," said Peter Willis, the project's principal investigator also at JPL. Molecules like amino acids come in two different "chiralties" that are mirror images of one another. Non-organic sources contain roughly equal "left-" and "right-handed" chirality amino acids, whereas amino acids from living organisms are predominantly left-handed - for life on Earth in any case. This differentiation can be detected by capillary electrophoresis. This method is exceedingly powerful for several reasons. Currently, NASA is putting great efforts into looking for habitable environments on Mars. We know that the Red Planet used to be a very wet place and there's evidence that suggests very briny sources of liquid water exists to this day. If life has ever taken hold on Mars, and if a future mission can directly sample this salty, toxic water, it's sensitive chemical analyses such as this that will likely track it down. Also, in the future, it is hoped that a mission may be sent to Jupiter's moon Europa, which is known to possess an extensive subsurface ocean. Many components for life as we know it exists on Europa, so if a robotic mission can be sent to the moon's ice-encrusted surface, or even dropped into the ocean itself, finding out whether there's life elsewhere in the solar system could be one simple chemistry test away. 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INTRODUCTION ============ Helicobacter pylori, a Gram-negative human pathogen, colonizes the stomach and is associated with several gastrointestinal disorders including peptic ulcers and gastric cancers ([@B1]). Over half of the world\'s population is estimated to harbor H. pylori, but only 15--20% of those infected develop severe disease. Helicobacter pylori is known for its remarkably high level of genetic diversity. A comparison of the fully sequenced genomes of three clinical isolates revealed substantial differences in chromosomal structure and a large number of genes that are variably present or absent among strains (up to 25% of the total coding regions) ([@B2],[@B3]). These observations have raised many questions, including how genetic diversity is generated in H. pylori and how variable genes contribute to disease outcome. One class of highly variable genes are restriction--modification (R--M) systems ([@B2]), which are typically composed of both a restriction endonuclease (REase) and a cognate DNA methyltransferase (MTase). Generally, the REase cleaves a specific DNA sequence unless it is methylated by the cognate MTase. R--M systems have been divided in type I, II or III, according to their cofactor requirement, molecular structure, mode of action and structure of the recognition sequence site ([@B4]). Typical type II R--M systems consist of two independent enzymes that act on the same sequence, usually a 4- to 8-bp palindrome. The recent sequencing of more than 400 bacterial and archaeal genomes has revealed that ∼90% of the genomes contain at least one R--M system and over 80% contain multiple R--M systems ([@B5]), but only a small fraction have been comprehensively studied. The H. pylori chromosome encodes a large number of active and inactive R--M systems. Analysis of the sequenced genomes of H. pylori strain 26695 and J99 predicted 26 putative R--M systems including 14 and 16 type II R--M systems, respectively. Comparative genomics of these systems suggests they have a high degree of sequence heterogeneity and that only a small fraction retained full activity ([@B6],[@B7]). Interestingly, for some R--M systems, MTase activity may be preserved despite inactivation of the respective REase. Although still under debate, R--M systems may carry out several biological roles. They have traditionally been implicated in bacterial defense from bacteriophage infection, which have in turn evolved a variety of anti-restriction defense mechanisms ([@B8]). R--M systems also regulate genetic exchange among bacteria, particularly relevant for bacteria like H. pylori that are naturally competent for DNA uptake ([@B9]). By constituting an effective barrier against DNA transformation in a bacterial population, R--M systems may provide the genetic isolation required for adaptation of the organisms to a special ecological niche ([@B10]). Paradoxically, R--M systems were also suggested to promote homologous recombination from the small DNA fragments produced by the incomplete digestion of incoming DNA by REases ([@B11]). Kobayashi and colleagues have suggested that R--M systems have attributes of selfish genes, and may act as invasive elements independent of any selective advantage to their host ([@B12],[@B13]). This hypothesis emerged from the findings that several R--M systems are horizontally transferred and that a fully active type II R--M system cannot easily be lost from its host because of postsegregational killing. Finally, DNA methylation may have important biological properties independent of the endonuclease function by regulating the interactions between proteins and DNA, in a similar manner to the stand-alone DNA methyltransferase Dam in both α- and γ-Proteobacteria ([@B14],[@B15]). In H. pylori, R--M systems may carry out other biological roles. Several R--M systems have been classified as 'chronic atrophic gastritis (ChAG) associated genes' by comparing the genome content of eight ChAG strains to a H. pylori 'pangenome' defined previously ([@B3],[@B16]). Other R--M genes were acid-regulated ([@B3]), undergo phase variation ([@B17],[@B18]) and several R--M systems were identified as candidate colonization factors using a mouse model of infection ([@B19]). Expression of the REase encoded by gene iceA1 was upregulated upon contact with gastric epithelial cells and its presence was associated with peptidic ulcer disease ([@B20]). A mutant in the endonuclease R.HpyC1I, isolated from H. pylori clinical isolate NTUH-C1, exhibited cell elongation and decreased adherence to a gastric cell line ([@B21]). In another report, DNA methylation by M.HpyAIV was shown to alter transcription of a selected number of genes including catalase (katA) ([@B22]). Here, we annotate a previously uncharacterized H. pylori R--M system M.HpyAXII/R.HpyAXII encoded by the locus HP0502/0503/0504/0505. We present biochemical and genetic analyses of this R--M system. We additionally explored its conservation among clinical isolates and its role during establishment of infection to query alternative biological functions of M.HpyAXII/R.HpyAXII. MATERIALS AND METHODS ===================== Bacterial strains and growth conditions --------------------------------------- Helicobacter pylori strains ([Supplementary Table S1](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)) were grown on solid horse blood agar (HB) plates containing 4% Columbia agar base (Oxoid, Hampshire, UK), 5% defibrinated horse blood (HemoStat Labs, Dixon, CA), 0.2% β-cyclodextrin (Sigma, St Louis, MO), 10 µg/ml vancomycin (Sigma), 5 µg/ml cefsulodin (Sigma), 2.5 U/ml polymyxin B (Sigma), 5 µg/ml trimethoprim (Sigma) and 8 µg/ml amphotericin B (Sigma) at 37°C either under a microaerobic atmosphere generated using a CampyGen sachet (Oxoid) in a gas pack jar or in an incubator equilibrated with 14% CO~2~ and 86% air. For liquid culture, H. pylori was grown in Brucella broth (Difco, Franklin Lakes, NJ) containing 10% fetal bovine serum (BB10; Invitrogen, Carlsbad, CA) with shaking in a gas pack jar containing a CampyGen sachet. For resistance marker selections, bacterial media were additionally supplemented with 15 µg/ml chloramphenicol (Cm, Sigma), 25 µg/ml kanamycin (Kan, Fisher Scientific, Pittsburgh, PA) or 60 mg/ml sucrose (Fisher Scientific). When culturing bacteria from mouse stomachs, 200 μg/ml bacitracin (Sigma) was added to eliminate normal mouse microbiota contamination. DNA manipulations ----------------- DNA manipulations, such as restriction digestion, PCR and agarose gel electrophoresis, were performed according to standard procedures ([@B23]). Helicobacter pylori genomic DNA was prepared by Wizard genomic DNA preparation kits (Promega, Madison, WI). Primers used for PCR and sequencing are in [Supplementary Table S2](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1). Plasmid DNA ([Supplementary Table S3](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)) was isolated and prepared from Escherichia coli or H. pylori using Qiagen Midiprep kit (Qiagen, Valencia, CA). Sequencing of plasmid DNA and PCR products was performed by the FHCRC Genomics Shared Resource and the resulting sequences analyzed using Sequencher (Gene Codes Corporation, Ann Harbor, MI). Generation of H. pylori knockout isogenic mutants --------------------------------------------------- Knockout alleles were constructed using a vector-free allelic replacement strategy to generate alleles in which a chloramphenicol acetyl transferase (cat) resistance cassette ([@B24]), a nonpolar kanamycin resistance (aphA3) cassette ([@B25]), or a cat cassette fused to a sucrose sensitivity marker (sacB) ([@B26]) replaced 80--90% of the coding sequence of the gene while preserving the start and stop codons. The primers used for this procedure are designated as 1 through 4 and are given in [Supplementary Table S2](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1). The catsacB cassette was generated by fusing cat to sacB with elimination of the terminator sequence using PCR (primers C2SA4 and SB1). After natural transformation ([@B27]) with the appropriate PCR product and selection on Cm- or Kan- containing media, four clones were evaluated by PCR to confirm replacement of the wild-type allele with the null allele. Urease activity and flagella-based motility were also confirmed for all the clones generated. Single clones were used for infection experiments and phenotypic characterization. Generation of H. pylori knockin isogenic mutants -------------------------------------------------- Null alleles generated by replacement with the catsacB cassette were subsequently replaced with alternate alleles by sucrose counter-selection. H. pylori strain NSH57 ΔhpyAXIIM/R::catsacB was naturally transformed with the appropriate plasmid or genomic DNA, and recombinants were selected on sucrose-containing HB plates, screened on Cm-containing media, and evaluated by PCR to confirm they lost the catsacB cassette. Site-directed mutagenesis ------------------------- To generate a catalytically inactive DNA MTase in H. pylori strain NSH57, an asparagine in conserved motif IV was replaced by alanine (N87A). A DNA fragment including hpyAXIIM/R was amplified from NSH57 by PCR and cloned into TA vector pCR-TOPO (TOPO cloning, Invitrogen). pCR-TOPO/hpyAXII was digested with EcoRI (NEB, Ipswich, MA) and subcloned into plasmid Bluescript SK+ (Stratagene, La Jolla, CA). Site-directed mutagenesis was performed on hpyAXIIM using the QuikChange kit (Stratagene) following the manufacturer instructions and confirmed by sequencing. Natural transformation ---------------------- H. pylori bacteria were freshly grown for 24--32 h on HB plates, transferred as patches onto fresh plates and grown for an additional 6--8 h. Donor DNA (plasmid, genomic or PCR product) was diluted as appropriate in distilled water and 10 μl was added to each patch and incubated overnight. The transformation mixture was harvested from the plate surface and resuspended in 350 μl phosphate buffer saline (PBS). Serial 10-fold dilutions were inoculated onto selective or nonselective HB plates. Transformation frequency was calculated as the number of Kan or Cm resistant colonies per recipient cell per nanogram of donor DNA. Expression of M.HpyAXII and R.HpyAXII proteins ---------------------------------------------- hpyAXIIM was amplified from DNA of wild-type NSH57 and NSH79 H. pylori by PCR and cloned into a pET-15b vector (Novagen, Gibbstown, NJ) in frame with the N-terminal His-Tag sequence using NdeI and XhoI (New England Biolabs). The resulting pET15b/hpyAXIIM plasmids were transformed into E. coli strain ER2925(DE3), derived from strain ER2925 \[NEB and ([@B28])\] and engineered to become a λDE3 lysogen using a lysogenization kit (Novagen). Plasmid pET15b/hpyAXIIR was transformed into E. coli strain BL21CodonPlus(DE3)-RIL. Protein expression was induced using 1 mM isopropyl-1-thio-β-[d]{.smallcaps}-galactopyranoside (IPTG) induction for 3 h at 37°C for M.HpyAXII and overnight at 16°C for R.HpyAXII to minimize endonuclease activity. Bacterial pellets were resuspended in lysis buffer (50 mM Tris pH 7.9, 100 mM NaCl, 1 mM DTT, 2% glycerol), incubated with 1 mg/ml lysozyme (Sigma) for 30 min on ice, and sonicated. For R.HpyAXII, soluble and insoluble fractions were separated by centrifugation at 18 000 r.p.m. for 20 min at 4°C. Antibody-based M.HpyAXII methylation activity assays ---------------------------------------------------- M. HpyAXII DNA MTase activity was assessed in a dot-blot assay using a rabbit primary antibody raised against DNA with N6-methyladenine (m6A) ([@B29]). Escherichia coli ER2925(DE3) transformed with pET15b and pET15b/hpyAXIIM was grown to log phase and induced with 1 mM IPTG for 3 h at 37°C. Genomic DNA of the cultures was isolated and 3 μl cross-linked to a nylon membrane (Hybond-XL, Amersham Biosciences, Piscataway, NJ) by UV (1.2 mJ/cm^2^ for 30 s). The membrane was blocked in a 3% nonfat dry milk solution and incubated with the m6A polyclonal rabbit antibody (1:10 000 dilution) overnight at 4°C. After a series of washes in PBST (PBS and 0.1% Tween-20), anti-rabbit IgG antibody conjugated to horseradish peroxidase (1:1000 dilution) was added to the membrane and detected using ECL Western Blotting reagent (Amersham Biosciences). Biochemical R.HpyAXII endonuclease activity assay ------------------------------------------------- One microliter of freshly prepared soluble fraction obtained from E. coli BL21(DE3) expressing R.HpyAXII was incubated for 3 h at 37°C with 500 ng E. coli ER2925 genomic DNA or pET15b plasmid DNA isolated from E. coli DH10B in presence of NEB buffer 1 (New England Biolabs). The product DNA was separated on a 0.8% agarose gel. Genetic R.HpyAXII endonuclease activity assay --------------------------------------------- To assess R.HpyAXII activity in a large number of H. pylori strains, we replaced the null allele in H. pylori strain NSH57ΔhpyAXIIM/R::catsacB with that from other strains as described above (Generation of H. pylori knockin isogenic mutants section). R.HpyAXII activity was determined by transforming these H. pylori clones with PCR constructs ΔhpyXIIM::cat and ΔHP0368::cat and enumerating recombinants recovered on Cm- containing HB plates. Mouse infections ---------------- Female C57BL/6 mice 24- to 28-days old were obtained from Charles River Laboratories and certified free of endogenous Helicobacter infection by the vendor. The mice were housed in sterilized microisolator cages with irradiated PMI 5053 rodent chow, autoclaved corn cob bedding, and acidified, reverse-osmosis purified water provided ad libitum. All studies were done under practices and procedures of Animal Biosafety Level 2. The facility is fully accredited by the Association for Assessment and Accreditation of Laboratory Animal Care, International, and all activities were approved by the FHCRC Institutional Animal Care and Use Committee. Competition experiments were performed as described previously ([@B24]) with 5.0 × 10^8^ bacteria of each strain in the inocula. In silico genomic analysis ---------------------------- Helicobacter pylori sequences were retrieved from the Comprehensive Microbial Resource (CMR) ([@B30]). Homologs of M. and R.HpyAXII and were sought using REBASE Blast, a tool of REBASE ([@B5]). Protein structure prediction analysis for M.HpyAXII and R.HpyAXII was carried out using the Protein Homology/Analogy Recognition Engine PHYRE ([@B31]). Sequence alignments were carried out with CLUSTALW2 ([@B32]) and 3D molecular structures were visualized and modified using PyMOL ([@B33]). The genome-wide distribution and frequency of GTAC sites was determined using genome-scale DNA pattern in Regulatory Sequence Analysis (RSA) Tools (<http://rsat.ulb.ac.be/rsat/>). For H. pylori strain NSH57, the sequence of the derivative strain G27 was used (D.A. Baltrus, M.R. Amieva, A. Covacci, D.S. Merrell, K. M. Ottemann, M. Stein, N.R. Salama, K. Guillemin, personal communication) and genomic GTAC sites were analyzed with the genome tools/restriction digest option of the CMR website. Sequences are available from the GenBank/EMBL/DDBJ databases with accession numbers FJ233107 to FJ233133. RESULTS ======= Structure-based prediction uncovers the existence of a novel H. pylori R--M system ------------------------------------------------------------------------------------ We set out to further characterize the HP0502/0503/0504/0505 locus that we previously identified in our genome-wide screen for candidate colonization factors ([@B19]). BLAST search of DNA sequences of these genes from H. pylori strain 26695 failed to identify any homologs. However, several lines of evidence suggested that HP0502/0503 encodes a DNA MTase and that it is organized in an R--M system along with the downstream gene, HP0504/0505. Nobusato et al. ([@B7]) previously predicted that this locus encodes a R--M system based on sequence analysis. In agreement with this finding, we used structure prediction algorithms of the program PHYRE ([@B31]) and found that the N-terminal domain of the HP0502/0503 polypeptides could be threaded onto a tertiary structure of the M.TaqI DNA MTase, crystallized from Thermus aquaticus ([Supplementary Figure S1](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1), E-value 6.1 × 10^−15^). Despite weak protein sequence homology, several amino acid motifs were shared between HP0502/0503 and M.TaqI ([Figure 1](#F1){ref-type="fig"}A) and mapped to the catalytic domain of M.TaqI ([Supplementary Figure S1](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)), further supporting the function of HP0502/0503 as an adenine MTase ([@B34]). More recently, the REase R.PabI from Pyrococcus abyssi was characterized and HP0504/0505 was identified as a homolog (28% protein sequence identity) and suggested to recognize the same target sequence, 5′-GTAC-3′ ([@B35]). Based on the proposed nomenclature for R--M systems ([@B4]), we have named this novel H. pylori R--M system M.HpyAXII/R.HpyAXII, encoded by genes hpyAXIIM and hpyAXIIR, respectively. Since R--M systems are highly polymorphic among H. pylori strains ([@B6]), we evaluated the genomic organization of M.HpyAXII/R.HpyAXII in several isolates. As illustrated in [Figure 1](#F1){ref-type="fig"}B, gene hpyAXIIM encodes a polypeptide of 331 amino acids and is predicted to be active in strains J99, HPAG1 and NSH57 but is likely inactive in 26695 and NSH79 where the expected protein products are truncated and fused with R.HpyAXII, respectively. Gene hpyAXIIR encodes a protein of 252 amino acids and is only expected to be functional in strains J99 and HPAG1 based on DNA sequences. Figure 1.Genomic organization of the HpyAXII R--M system. (A) Amino acid sequence alignment of 26695 HP0502/0503, NSH57 M.HpyAXII and M.TaqI from Thermus aquaticus reveals conserved motifs (highlighted in gray) in the N-terminal portion of the protein. (\) - identical residues, (:) conserved substitution, (.) semi-conserved substitution. (B) Genomic organization of genes hpyAXIIM* and hpyAXIIR in H. pylori strains 26695, J99, HPAG1 and two mouse adapted strains NSH57 and NSH79. The expected phenotype for this R-M system in each strain is given based on DNA sequences. M, DNA MTase; R, REase; +, active; --, inactive. M.HpyAXII is truncated in 26695 and fused to R.HpyAXII in NSH79. R.HpyAXII is truncated in 26695, partially deleted in NSH57 (dashed lines), and fused to M.HpyAXII in NSH79 (in-frame deletion represented with dashed lines). M.HpyAXII functions as a γ-adenine MTase ---------------------------------------- To validate the function of M.HpyAXII as a DNA MTase, we inducibly expressed Histidine-tagged M.HpyAXII from H. pylori strain NSH57 and Histidine-tagged M.HpyAXII fused to R.HpyAXII from strain NSH79 in E. coli ([Figure 2](#F2){ref-type="fig"}A). M.HpyAXII activity was studied using E. coli strain ER2925(DE3) ([Supplementary Table S1](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)), defective for all known R--M systems, and presumably harboring chromosomal DNA devoid of adenine or cytosine methylation (Materials and methods section). Genomic DNA from the E. coli cultures expressing M.HpyAXII was isolated and adenine methylation assessed using antibodies against N6-methyladenine. Adenine MTase activity could be detected when M.HpyAXII from NSH57 but not NSH79 was expressed in E. coli ([Figure 2](#F2){ref-type="fig"}B). The lack of MTase activity by NSH79 M.HpyAXII probably reflects the genetic rearrangements observed at the NSH79 locus ([Figure 1](#F1){ref-type="fig"}B). To further confirm that M.HpyAXII acts as an adenine MTase, we used site-directed mutagenesis on the predicted catalytic site of this enzyme. We identified conserved motif IV (D/N/S)PP(Y/F) \[[Figure 1](#F1){ref-type="fig"}A and ([@B34])\] and the substitution of asparagine with alanine (point mutation designated N87A) in NSH57 M.HpyAXII completely abolished adenine MTase activity without affecting the expression levels of this protein ([Supplementary Figure S2](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)). Along with our genomic data, this finding supports the re-annotation of this H. pylori protein as a γ-adenine MTase. Figure 2.Biochemical demonstration that HypAXII functions as an R--M system targeting GTAC sites. (A and B) NSH57 M.HpyAXII methylates genomic DNA on adenines when expressed in E. coli. (A) Escherichia coli ER2925(DE3) extracts expressing NSH57 or NSH79 M.HpyAXII (arrowheads) separated by SDS--PAGE gel and stained with Coomassie blue. Control - empty plasmid. Two separate E. coli clones (1 and 2) were analyzed. (B) The indicated amount of genomic DNA from the respective E. coli cultures was cross-linked to a nitrocellulose membrane. DNA N-6 adenine methylation (m6A) was detected using anti-m6A antibodies and showed a signal during NSH57 M.HpyAXII but not NSH79 M.HpyAXII expression. (C--F) The HpyAXII R--M system targets the tetramer 5′-GTAC-3′. (C) Helicobacter pylori strain NSH57 wild-type and ΔhpyAXIIM genomic DNA was isolated and digested with RsaI. Agarose gel separation showed fragmentation for ΔhpyAXIIM genomic DNA but not wild-type. (D) hpyAXIIR from H. pylori strain HPAG1 was cloned and expressed E. coli BL21(DE3) under inducible conditions. Soluble (sol) and insoluble (insol) fractions were separated by SDS--PAGE gel and stained with Coomassie blue. R.HpyAXII was mostly insoluble (arrowhead). Control, empty plasmid. The soluble fractions shown in C were incubated with unmethylated genomic DNA (E) or plasmid DNA (F) and separated by agarose gel. DNA fragmentation was only observed when R.HpyAXII was expressed. Similar DNA restriction patterns (F) indicate that these enzymes cleave the same DNA sequence. Bands of higher sizes seen for with R.HpyAXII suggest incomplete digestion. Two separate E. coli clones are shown (1 and 2). The HpyAXII R-M system targets the tetramer 5′-GTAC-3′ ------------------------------------------------------ Two independent approaches defined the target sequence of this novel R--M system. First, using an array of methylation-sensitive endonucleases, we sought to identify an enzyme that could digest H. pylori NSH57 chromosomal DNA isolated from a ΔhpyAXIIM mutant but not from wild-type. Only the enzyme RsaI digested DNA from the ΔhpyAXIIM::cat mutant but not wild-type ([Figure 2](#F2){ref-type="fig"}C), indicating that the DNA MTase M.HpyAXII and the endonuclease RsaI act on the same target sequence, 5′-GTAC-3′, where the adenine residue is methylated by M.HpyAXII. Using this result, we investigated M.HpyAXII activity in the H. pylori strains where the HpyAXII R-M system was sequenced ([Figure 1](#F1){ref-type="fig"}B). Genomic DNA from H. pylori strains 26695 and NSH79 could be digested with RsaI, whereas J99, NSH57 and HPAG1 DNA were protected from RsaI digestion (data not shown), indicating that M.HpyAXII is only active in these three strains and agreeing with our predictions from the genomic sequences. RsaI digestion of DNA isolated from the NSH57hpyAXIIM^N87A^ mutant showed fragmentation when separated on agarose gel (data not shown), confirming that this single amino acid substitution abolishes MTase catalytic activity. In the second approach, we cloned and expressed the putative endonuclease gene hpyAXIIR in E. coli under the control of an inducible promoter ([Figure 2](#F2){ref-type="fig"}D). We chose hpyAXIIR from H. pylori strain HPAG1 because this protein is expected to be functional based on sequence analysis ([Figure 1](#F1){ref-type="fig"}). Incubation of the E. coli soluble fraction expressing HPAG1 R.HpyAXII with genomic DNA unmethylated for GTAC sites showed endonuclease activity as indicated by the resulting smear on agarose gel ([Figure 2](#F2){ref-type="fig"}E). To determine R.HpyAXII cleavage site, the same experiment was carried out with unmethylated plasmid DNA. R.HpyAXII-containing extract cleaved plasmid DNA and gave an identical fragmentation pattern as RsaI ([Figure 2](#F2){ref-type="fig"}F) confirming that R.HpyAXII acts on GTAC sites. In contrast to HPAG1 R.HpyAXII, no endonuclease activity was detected when R.HpyAXII from H. pylori strain J99 was expressed in E. coli (data not shown). While the exact cutting site of R.HpyAXII within the tetramer GTAC remains to be defined, our demonstration that hpyAXIIM and hpyAXIIR encode two independent enzymes suggests that they together constitute a class II R-M system ([@B4]). GTAC sites are scarce in the H. pylori chromosome but are found at high frequency in the rDNA genes ----------------------------------------------------------------------------------------------------- We determined the frequency and distribution of GTAC sites in four sequenced strains of Helicobacter pylori: 26695 (122 sites), J99 (184 sites), HPAG1 (114 sites), G27 (115 sites). This total number of sites is \>50-fold lower than the expected number based on frequency of nucleotides and confirms previous observations ([@B35]). Interestingly, a significant fraction of the GTAC sites are located within the ribosomal RNA (rRNA) genes. The 23SrRNA contains eight or nine sites depending on the strain analyzed and the 16SrRNA contains two sites ([Table 1](#T1){ref-type="table"}). Since two copies of each gene exist in the H. pylori chromosome, a total of 20 or 22 GTAC sites are located within the rRNA genes. We were particularly interested in GTAC sites that are strictly conserved among H. pylori strains since they may be biologically important. Of all intragenic sites, ten are conserved in all four H. pylori strains and can be mapped to a total of 10 genes that belong to various functional categories ([Table 1](#T1){ref-type="table"}). Interestingly, three of these genes belong to the cag pathogenicity island (cagT, cagL and cagH). Some of these sites are located in the promoter region of genes and may influence transcription efficiency. Table 1.Distribution of all conserved GTAC sites in four H. pylori strainsGene number[^a^](#TF1){ref-type="table-fn"}Gene name[^a^](#TF1){ref-type="table-fn"}Gene descriptionCharacteristics[^b^](#TF2){ref-type="table-fn"}23S rDNARibosomal DNA8 sites16S rDNARibosomal DNA2 sitesHP0200rpl32Predicted ribosomal protein L328 bp after start of HP0200 and 200 bp from start of HP0201HP0486hofCOuter membrane proteinHP0499pldAPhospholipase A1 precursorHP0532cagTcag pathogenicity island protein THP0539cagLcag pathogenicity island protein L200 bp from start of cagIHP0541cagHcag pathogenicity island protein HHP0613Predicted ABC transporter87 bp after start of HP0613HP0630mda66Modulator of drug activity11 bp after start of HP0630 and 170 bp from start of HP0631HP1197rps12Predicted ribosomal protein S12190 bp from start of HP1198HP1228invADiadenosine polyphosphate hydrolase50 bp from start of HP1229[^1][^2] The HpyAXII R-M system effectively restricts incoming plasmid DNA ----------------------------------------------------------------- Bacterial R--M systems protect host genomes from invading DNA such as viral, plasmid and other foreign DNA by cleaving exogenous DNA at specific sites when unmethylated. We determined whether the endonuclease R.HpyAXII could restrict incoming plasmid DNA during natural transformation of H. pylori. As shown above, R.HpyAXII is biochemically active in H. pylori HPAG1, a strain difficult to transform (data not shown). We thus replaced the endogenous locus encoding M.HpyAXII/R.HpyAXII in the easily transformable NSH57 strain with that from HPAG1 (Materials and methods section). This engineered strain, NSH57hpyAXIIM/R~HPAG1~, encodes a fully active HpyAXII R-M system (R + M + phenotype). For comparison, we deleted the endonuclease component R.HpyAXII in the same strain and replaced it with an antibiotic resistance cassette to create a null allele (ΔhpyAXIIR::aphA3, R--M + phenotype). As donor DNA, we used plasmid pTM113-cat (Materials and methods and [Supplementary TableS3](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)) that we isolated from H. pylori strain NSH57 wild-type (fully methylated, denoted 'M+'), from the catalytically inactive mutant NSH57hpyAXIIM^N87A^ (unmethylated for GTAC sites, denoted 'M−'), or from E. coli (unmethylated at all sites, denoted 'all M−'). We first verified that the numerous R--M systems encoded by H. pylori strain NSH57 could effectively restrict unmethylated (all M−) plasmid DNA as compared to methylated (M+) plasmid. Transformation frequency of wild-type H. pylori NSH57 decreased over 200-fold when completely unmethylated plasmid DNA prepared from E. coli was used as compared to methylated (M+) plasmid (data not shown), in agreement with previous work ([@B37]). We similarly found that transformation frequency involving M− plasmid decreased over 60-fold in the bacteria harboring an active R.HpyAXII endonuclease (R+) (ratio R−/R+, [Table 2](#T2){ref-type="table"}), demonstrating that this enzyme constitutes an effective barrier against incoming plasmid DNA in vivo. Table 2.R.HpyAXII effectively restricts incoming plasmid DNADonor DNA[^a^](#TF3){ref-type="table-fn"}Transformation frequency (\# transformants/recipient cell/ng × 10^−8^)[^b^](#TF4){ref-type="table-fn"}, mean (SEM)RatioRecipient strain[^c^](#TF5){ref-type="table-fn"}R+R−R−/R+M−12 (8.8)760 (120)63M+1900 (400)2500 (180)1.3[^3][^4][^5] The HpyAXII R--M system effectively restricts incoming chromosomal DNA ---------------------------------------------------------------------- To investigate the role of the endonuclease R.HpyAXII in restricting incoming chromosomal DNA in vivo, we assessed transformation using donor genomic DNA harboring a kanamycin resistance marker (aphA3) at the 23S rDNA locus. This marker contains a GTAC site and is susceptible to cleavage by R.HpyAXII. As described for plasmid DNA, donor chromosomal DNA was isolated from bacteria encoding an active (M+) or inactive (M−) M.HpyAXII MTase. We determined if the endonuclease R.HpyAXII could restrict incoming chromosomal DNA by comparing transformation efficiency in NSH57 harboring either an active (R+) or inactive (R−) restriction endonuclease R.HpyAXII. When genomic DNA isolated from H. pylori lacking M.HpyAXII MTase activity (M−) was transformed into the bacteria harboring an active R.HpyAXII endonuclease (R+), a 240-fold decrease in transformation frequency was observed (R−/R+, [Table 3](#T3){ref-type="table"}). We also digested the same donor genomic DNA in vitro with RsaI prior to transformation, which lowered the transformation frequency further to undetectable levels ([Table 3](#T3){ref-type="table"}). We suggest that cleavage of the GTAC site in gene aphA3 by the endonucleases RsaI and R.HpyAXII inactivates this marker and results in the subsequent decrease in transformation frequency. Overall, we demonstrated that active R.HpyAXII endonuclease effectively limits the incorporation of unmethylated exogenous homologous DNA into the H. pylori chromosome. Table 3.R.HpyAXII effectively restricts incoming genomic DNADonor DNA[^a^](#TF6){ref-type="table-fn"}Transformation frequency (\# transformants/recipient cell/ng × 10^−10^)[^b^](#TF7){ref-type="table-fn"}, mean (SEM)RatioRecipient strain[^c^](#TF8){ref-type="table-fn"}R +R−R−/R+M+18 (0.16)44 ([@B17])2.4M+ RsaI49 (9.3)95 ([@B30])1.9M−0.42 (0.26)100 ([@B11])240M− RsaI01.4 (0.60)inf [^d^](#TF9){ref-type="table-fn"}[^6][^7][^8][^9] The HpyAXII R--M system follows the selfish hypothesis ------------------------------------------------------ Kobayashi and colleagues suggested that type II R--M systems act as selfish genetic elements and cannot be easily replaced with a homologous stretch of DNA ([@B36]). This phenomenon, more commonly known as postsegregational killing, has been attributed to the gradual dilution of the modification and restriction enzymes in the descendants of the cell that lost the R--M system. Since there is asymmetry between the roles of the MTase and REase, newly replicated chromosomes will be inadequately protected by methylation and rendered susceptible to cleavage by the residual REase, leading to cell death. To determine whether the type II HpyAXII R--M system follows the selfish hypothesis, we deleted this chromosomal locus by allelic replacement from H. pylori strain NSH57 engineered to harbor an active (R+) or inactive (R−) R.HpyAXII endonuclease. We found that R− but not R+ recipient bacteria were easily transformed with donor NSH57 genomic DNA in which hpyAXIIM/R was replaced with a catsacB marker (strain NSH57 ΔhpyAXIIM/R::catsacB) ([Table 4](#T4){ref-type="table"}, ΔhpyAXIIM/R::catsacB). This 2100-fold decrease in transformation frequency seen for the R + recipient strain is independent of the digestion of GTAC sites in the donor DNA because they are fully protected by DNA methylation. We verified that the recipient strains were not generally defective at transforming DNA by showing allelic replacement at a different chromosomal region (ΔHP0368). In summary, we showed that chromosomal type II HpyAXII R--M system resists its replacement with an empty site in the presence of the active endonuclease R.HpyAXII, as described for other bacterial type II R--M systems ([@B38],[@B39]). Table 4.The HpyAXII R-M system follows the selfish hypothesisDonor DNATransformation frequency (\# transformants/recipient cell/ng DNA × 10^−10^)[^c^](#TF12){ref-type="table-fn"}, mean (SEM)RatioRecipient strain[^d^](#TF13){ref-type="table-fn"}R+R−R−/R+ΔhpyAXIIM/R::catsacB[^a^](#TF10){ref-type="table-fn"}0.15 (0.08)[^e^](#TF15){ref-type="table-fn"}320 ([@B21])2100ΔhpyAXIIM::cat[^b^](#TF11){ref-type="table-fn"}0.17 (0.17)[^f^](#TF15){ref-type="table-fn"}1100 (350)6500ΔHP0368::cat[^b^](#TF11){ref-type="table-fn"}310 (9.2)180 ([@B38])0.58[^10][^11][^12][^13][^14][^15] An active R.HpyAXII REase can only exist in the presence of its active DNA MTase partner ---------------------------------------------------------------------------------------- We predicted that bacteria harboring a functional REase must also encode an active cognate DNA MTase to protect the genome from digestion. The R + M− phenotype should therefore be lethal, a condition especially relevant for the HpyAXII R-M system since many of the cognate sites are present within the rRNA genes ([Table 1](#T1){ref-type="table"}). Thus we deleted hpyAXIIM by allelic replacement using the ΔhpyAXIIM::cat PCR construct in bacteria harboring active (R+) or inactive (R−) endonuclease R.HpyAXII ([Supplementary Figure S3](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)). We observed a dramatic reduction in transformation efficiency (6500-fold) for the R + bacteria ([Table 4](#T4){ref-type="table"}). In comparison, allelic replacement at a different chromosomal region (ΔHP0368) was carried out at a similar efficiency in R + and R- bacteria ([Table 4](#T4){ref-type="table"}). Importantly, the observed decrease in transformation efficiency is independent of the cleavage of incoming ΔhpyAXIIM::cat donor DNA by the endonuclease R.HpyAXII since this fragment is devoid of GTAC sites. Rather, recombinants for the R+ bacteria probably died from double-stranded breaks in their chromosomal DNA. We were intrigued by the rare transformants obtained when gene hpyAXIIM was deleted in the R+ bacteria because it suggests that the R+M− phenotype is occasionally viable. We investigated these clones further and found evidence of gene amplification and adaptive mutations at the M.HpyAXII/R.HpyAXII locus. From three independent transformations, we analyzed a total of 16 clones; seven displayed evidence of gene amplification and nine showed adaptive mutations. For gene amplification, hpyAXIIM was present in both a wild-type and a mutated form at the same locus ([Supplementary Figure S3](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)), overall resulting in the phenotype R+ M+. This diploidy for hpyAXIIM was unstable and the mutant form of the gene was generally lost after several passages in vitro (data not shown). In other clones, point mutations were found in the promoter region of gene hpyAXIIR, specifically in the ribosome binding sequence and in the start codon of the gene ([Figure 3](#F3){ref-type="fig"}). In all cases, these mutations likely prevent effective translation of the endonuclease R.HpyAXII; the overall phenotype of these clones therefore became R−M−. We conclude that H. pylori bacteria only harbor an active R.HpyAXII endonuclease in the presence of an active M.HpyAXII MTase. Figure 3.Deletion of hpyAXIIM from a H. pylori strain harboring an active endonuclease R.HpyAXII yielded rare transformants that display adaptive mutations in the promoter region of hpyAXIIR. Gene hpyAXIIR was sequenced in nine surviving recombinants obtained following hpyAXIIM deletion. When compared to wild-type, single base deletions and substitutions (highlighted in gray) were detected in the transformants in both the ribosomal binding site (RBS) and start codon (START) of hpyAXIIR. The adenine MTase M.HpyAXII is highly conserved among H. pylori strains ------------------------------------------------------------------------- Helicobacter pylori R--M systems are remarkably heterogeneous among strains. Some are present in a fraction of strains, absent in others, or inactivated by deletion or frameshift mutations. It has been estimated that less than one-third of H. pylori R--M systems are fully active ([@B6]). We were interested in determining whether M.HpyAXII is present and active in a panel of H. pylori clinical isolates. We found that the HpyAXII R--M system is well conserved as we amplified this locus from all 50 pediatric clinical isolates isolated from 47 patients (S. Talarico, J. Fero, D.T. Thompson, J. Guarner, S. Czinn. B.D. Gold, N.R. Salama, personal communication) though its size was reduced in four (8%) strains (data not shown). To assess M.HpyAXII MTase activity for the clinical isolates, we digested each strain\'s genomic DNA with the REase RsaI, which only cleaves unmethylated GTAC sites. Of the 50 clinical isolates DNA, only four strains were digested with RsaI, all of which displayed a smaller amplified product for the HpyAXII R--M system (data not shown). M.HpyAXII activity is therefore remarkably conserved among H. pylori strains (92% active as tested). To determine how M.HpyAXII was inactivated in the four H. pylori strains lacking DNA MTase activity, we sequenced the HpyAXII R--M system. In all strains, most of hpyAXIIM and hpyAXIIR coding region was substituted by a gene in reverse orientation ([Figure 4](#F4){ref-type="fig"}). This replacing gene, that we name hrgC (HpyAXII replacing gene C), shows strong homology to Helicobacter acinonychis sheeba Hac_1467 (80% nucleotide identity). Hac_1467 is present at a different chromosomal region in this species (557 kb away from the HpyAXII locus) and encodes a 94 amino acid protein of unknown function. In the four clinical isolates where gene replacement occurred, hrgC encodes a protein of 94- or 128-amino acids. A search for orthologs of Hac_1467 at the H. acinonychis locus using a PCR approach was negative for all 50 clinical isolates and only positive for H. pylori strain NSH57. Surprisingly, in both H. acinonychis sheeba and H. pylori NSH57, Hac_1467 is preceded by a 165 bp DNA fragment (Hac_1466) that shows high homology to the 5′-end of hpyAXIIM (89% sequence identity, [Figure 4](#F4){ref-type="fig"}), suggesting that some recombination event took place at this locus. In summary, we demonstrated that the activity of the DNA MTase M.HpyAXII is highly conserved among H. pylori strains but can be disrupted by insertion of the alternate gene hrgC at the same locus in several unrelated strains. Figure 4.M.HpyAXII MTase activity is occasionally disrupted by insertion of the alternate gene hrgC. The HpyAXII R--M system was sequenced in the H. pylori clinical isolates where M.HpyAXII was found inactivated (M−). In all M− strains, most of the HpyAXII locus was replaced with alternate gene hrgC that shows strong homology to Hac_1467 (80% nucleotide identity) from Helicobacter acinonychis sheeba. Depending on the strain analyzed, gene hrgC is either 285- or 387-bp long. The REase R.HpyAXII is poorly conserved among H. pylori strains ----------------------------------------------------------------- The conservation of M.HpyAXII MTase activity in H. pylori isolates led us to evaluate R.HpyAXII activity in these same isolates. We developed a genetic assay to assess R.HpyAXII endonuclease activity based on the previous finding that the MTase M.HpyAXII cannot be deleted in the presence of an active REase. Since H. pylori strains vary in their ability to be transformed by exogenous DNA, we chose to engineer strain NSH57 to contain the HpyAXII R-M system from the different clinical isolates using allelic replacement and a knockin approach (Materials and methods section). We transformed the resulting clones with the ΔhpyAXIIM::cat donor DNA to delete gene hpyAXIIM. When a large number of transformants were recovered, we deduced that R.HpyAXII from that particular strain lost endonuclease activity. In contrast, when few or no transformants were obtained, we concluded that R.HpyAXII must be active because of the lethality of the R + M− phenotype. The DNA fragment ΔHP0368 was used as transformation control. We first evaluated R.HpyAXII activity in the NSH57 clones engineered to contain the HpyAXII R-M system from H. pylori strains NSH57, J99, NSH79 and HPAG1. As expected from our genomic and biochemical results ([Figures 1](#F1){ref-type="fig"}B and [2](#F2){ref-type="fig"}), only the clone harboring the HpyAXII R--M system from strain HPAG1 showed a dramatic reduction in transformation efficiency when gene hpyAXIIM was deleted ([Supplementary Figure S4](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)). In contrast, clones harboring HpyAXII from strain NSH57, NSH79 and J99 yielded a large number of transformants, confirming that the endonuclease R.HpyAXII is inactive in these strains. This result therefore validates the use of our genetic assay to investigate R.HpyAXII endonuclease activity. We constructed NSH57 clones harboring the HpyAXII R-M system from 37 clinical isolates and found that R.HpyAXII was only active in seven clones (18.9%) based on the number of transformants recovered. All strains could successfully be transformed with the ΔHP0368 PCR product, ruling out a general defect in transformation. We examined the nature of mutations that inactivated R.HpyAXII in the 30 H. pylori isolates by sequencing gene hpyAXIIR: nine strains (30%) contain a large deletion (39AA) similar to the one found in strain NSH57 ([Figure 1](#F1){ref-type="fig"}B), seven strains (23%) harbor nonsense mutations that result in a truncated protein, two strains (7%) have both the deletion and nonsense mutations, and 12 strains (40%) contain single nucleotide polymorphisms (SNPs) in the coding region of gene hpyAXIIR. For four strains, we confirmed that the hpyAXIIR sequence was identical in the engineered strain and in the original isolate, ruling out the possibility that mutations were introduced during the genetic manipulations. To analyze the inactivating SNPs in more details, we aligned the protein sequences from the 12 inactive and seven active R.HpyAXII enzymes with that of H. pylori strain HPAG1, shown to be active. We identified between two and five amino acid substitutions per strain that may inactivate R.HpyAXII function, resulting in a total of 31 distinct coding SNPs. The nature and frequency of these substitutions are described in [Figure 5](#F5){ref-type="fig"}A and the SNPs for each strain are described in [Supplementary Table S3](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1). These coding SNPs were mapped on the primary protein sequence of R.HpyAXII ([Figure 5](#F5){ref-type="fig"}B) as well as on the three-dimensional model based on R.PabI crystal structure ([Figure 5](#F5){ref-type="fig"}C) ([@B40]). Out of these 31 SNPs, two (\#5 and \#18) overlap with residues previously shown to be required for R.PabI activity ([@B40]), and seven are found in multiple H. pylori strains ([Figure 5](#F5){ref-type="fig"}A). Several structural motifs (β3, α3, β6, β8, β10 and α4 based on R.PabI) contain a high density of SNPs and may be crucial for R.HpyAXII endonuclease activity. Figure 5.Protein sequence analysis of 12 inactive R.HpyAXII enzymes reveal 31 distinct coding SNPs. (A) Comparison of R.HpyAXII protein sequences in 12 H. pylori strains harboring inactive enzyme and in seven strains harboring active enzyme with that from strain HPAG1 identified 31 coding SNPs, enumerated \#1 through \#31 with the conservation and frequency of each substitution indicated. (C) - conserved, (S) - semiconserved, (-) - unrelated. Changes highlighted in gray were found in multiple strains and changes highlighted in purple were previously shown to be required for R.PabI activity ([@B40]). (B) HPAG1 R.HpyAXII and R.PabI protein sequences were aligned and the position of each SNP highlighted. Red, potentially inactivating SNPs numbered \#1 through \#31; cyan, previously shown to be required for R.PabI activity and target the predicted DNA-binding domain; purple, coding SNPs in R.HpyAXII also required for R.PabI activity. (\) - identical residues, (:) - conserved substitution, and (.) semi-conserved substitution. (C) Coding SNPs were mapped on the three-dimensional model generated for R.HpyAXII based on the R.PabI crystal structure using the same color code used in (B). H. pylori* M.HpyAXII MTase activity is not required for establishing infection in mice --------------------------------------------------------------------------------------- The remarkable preservation of M.HpyAXII activity in H. pylori strains and the intriguing distribution of chromosomal GTAC sites led us to investigate whether this DNA MTase confers a selective advantage to H. pylori during infection. We were also interested in determining whether M.HpyAXII has a role during infection that is independent of its DNA MTase activity. For this reason, we infected mice with H. pylori NSH57 deletion mutant (ΔhpyAXIIM::cat) and with the catalytically inactive mutant (hpyAXIIM^N87A^), which MTase can presumably still bind DNA but not methylate it. Mouse stomachs were harvested after one week of infection and viable bacteria were recovered and enumerated to calculate the competitive index for each infection \[colony forming units (CFU) mutant bacteria/CFU wild-type bacteria\] (Materials and methods section). When mice were infected with NSH57ΔhpyAXIIM::cat mutant and wild-type bacteria, equal number of bacteria were recovered (n = 9, [Figure 6](#F6){ref-type="fig"} left) indicating that they could establish infection at a similar efficiency. M.HpyAXII protein expression is therefore not required for establishing infection in H. pylori strain NSH57. We also infected mice in competition with the catalytically inactive mutant hpyAXII^N87A^ and the deletion mutant ΔhpyAXIIM::cat. Both strains infected mice similarly (n = 9, [Figure 6](#F6){ref-type="fig"} right) indicating that M.HpyAXII does not have a role during establishment of infection that is independent of its DNA MTase activity. Figure 6.M.HpyAXII MTase activity is not required by H. pylori for establishing infection in a mouse infection model. Mice were infected in 1:1 competition with the indicated H. pylori strains and the competitive index (CI) determined after one week of infection. The CI was calculated by dividing colony forming units (CFU) recovered of null mutant bacteria over CFU wild-type or point mutant bacteria and corrected by dividing the actual input ratio enumerated from plating the inoculums. Left, mice (n = 9) were infected with H. pylori NSH57 wild-type and an isogenic null mutant ΔhpyAXIIM::cat. Both strains infected mice at a similar efficiency (geometric mean CI slightly above one). Right, mice (n = 9) were infected with the NSH57ΔhpyAXIIM::cat mutant and the catalytically inactive mutant (hpyAXIIM^N87A^) constructed in strain NSH57. DISCUSSION ========== Helicobacter pylori naturally takes up exogenous DNA, a condition thought to promote genetic diversification by spreading new alleles in the population. However, genetic exchange is limited by the large number and heterogeneity of H. pylori R--M systems ([@B6]). The contribution of individual R--M systems in restricting incoming DNA remains for the most part undetermined since only a few of these systems have individually been tested in H. pylori ([@B37],[@B41]). In addition, it is possible that R--M systems carry out other biological roles. In our study, we have biochemically characterized a novel H. pylori type II R--M system, M.HpyAXII/R.HpyAXII, and showed that it targets GTAC sites thus confirming prior predictions ([@B35]). The endonuclease R.HpyAXII effectively restricted both unmethylated plasmid (60-fold) and genomic (240-fold) DNA ([Tables 2](#T2){ref-type="table"} and [3](#T3){ref-type="table"}). Our results agree with previous reports documenting effective restriction of plasmid DNA by R.HpyAIII (encoded by HP0091, GATC) ([@B37]), and of chromosomal DNA by R.HpyAII (encoded by HP1366, GAAGA) ([@B41]). Since R--M systems are highly polymorphic in H. pylori, we analyzed the conservation of both M.HpyAXII MTase and R.HpyAXII endonuclease activities in a panel of clinical isolates. We found a striking asymmetry between the highly conserved MTase activity (92% active, n = 50) and that of the REase (18.9% active, n = 37). In fact, our data indicate that M.HpyAXII is the third most highly conserved adenine MTase in H. pylori, preceded only by M.HpyAI (CATG, 100% conserved) and M.HpyAIII (GATC, 97% conserved) ([@B42],[@B43]). Other studies have suggested that MTase activities are generally selected for in H. pylori ([@B6],[@B29],[@B44]) but how DNA methylation benefits the organism is unknown. To begin to probe how M.HpyAXII affects H. pylori biology, we generated a null allele in gene hpyAXIIM in mouse-adapted strain NSH57 either by deletion or by targeted mutation of the catalytic site of the enzyme (hpyAXIIM^N87A^). Mouse infection with these strains indicated that M.HpyAXII expression is not required by H. pylori for the establishment of infection ([Figure 6](#F6){ref-type="fig"}) in contrast to previous work ([@B19]). As this study did not complement the mutant phenotype, it is possible that second site mutations or polar effects accounted for the defect observed. Further experiments are needed to determine if M.HpyAXII activity is important during persistent infection and to elucidate how GTAC methylation provides a selective advantage in H. pylori. It was proposed that the maintenance of an active MTase allows reactivation of a given R--M system through recombination with the genomic DNA of a strain that encodes an active REase. However, the probability of this event must be relatively low given that R.HpyAXII is active in a small number of strains. It was also postulated that 'orphan' MTases are conserved because they act as a 'molecular vaccine' against the parasitism of R--M systems. This hypothesis was based on the finding that Dcm in E. coli can alleviate postsegregational killing induced by the EcoRII R--M complex that recognizes the same sequence as Dcm ([@B45]). This also seems unlikely because no R--M system that acts on the same site as HpyAXII has been identified in H. pylori. DNA methylation may alternatively be selected for in H. pylori because it confers immunity from the action of the cognate REase and therefore increases the chances that an entire gene is successfully propagated in a population. However, the finding that the average size of recombined fragment is unusually small (417 bp) in H. pylori as compared to other bacteria indicates that incoming DNA is generally susceptible to cleavage by REases ([@B46]). Another important role of DNA methylation is to modulate the interaction between proteins and DNA as demonstrated for the stand-alone adenine MTase Dam in α- and γ-Proteobacteria ([@B14],[@B15],[@B47]). DNA MTases involved in R--M systems that are not coupled to an active REase may have evolved similar regulatory functions since they are no longer under the pressure to act on all chromosomal sites and may therefore preferentially methylate sequences required for transcription. The genome-wide analysis of conserved GTAC sites identified genes of various functional classes including several genes of the cag pathogenicity island but it is unknown whether their expression is affected by M.HpyAXII methylation. Although GTAC sites are scarce in the H. pylori chromosome, they are present at high frequency in the 23S and 16S rRNA genes. Our preliminary experiments showed no effect of M.HpyAXII methylation on 23S rRNA transcripts levels or on in vitro growth of the bacteria (data not shown), arguing against a role for GTAC methylation in H. pylori ribosomal biogenesis. It is possible that ribosomal GTAC sites are preserved because they are crucial for the folding of the RNA into functional secondary structures in Helicobacter species and that methylation of these sites does not have any biological role. In agreement with this hypothesis, the analysis of 23S rRNA sequences in 55 Helicobacter strains representing 41 taxa ([@B48]) shows conservation of most GTAC sites even though many of these species probably lack a M.HpyAXII enzyme. Alternatively, ribosomal GTAC sites may not have been erased from these chromosomal regions because they evolve at a different rate than the rest of the genome; these elements are duplicated in H. pylori and are subjected to homogenization processes such as gene conversion ([@B49]). Overall, the significance of ribosomal GTAC sites in H. pylori remains unsolved but echoes a similar anomaly in site distribution with the tetramer CTAG that is very rare in E. coli and in other proteobacterial genomes and over-represented in rRNA genes ([@B50],[@B51]). The comparison of tetranucleotide combinations in 27 representative microbial genomes revealed that ACGT, GTAC and TCGA are strongly underrepresented in both coding and noncoding DNA in H. pylori ([@B52]). A significant correlation between the avoidance of palindromic words and type II R--M systems was suggested ([@B53]) presumably because these systems exert significant pressure on an organism when restriction is intact but methylation is incomplete. However, the highly conserved H. pylori R--M systems M.HpyAI/iceA (CATG) or M.HpyAIII/R.HpyAIII (GATC) target sites are not underrepresented in the H. pylori genome. Since cognate site avoidance is probably dependent on the timing of acquisition of a given R--M system during evolution, the HpyAXII R--M system must have been acquired a long time ago, consistent with the finding that this system is present in all H. pylori isolates analyzed. Interestingly, GTAC sites are also scarce in the Helicobacter hepaticus genome even though it does not encode an M.HpyAXII/R.HpyAXII ortholog. This can either be explained by the recent loss of this system or by the existence of a different R--M system that acts on GTAC sites in H. hepaticus. Our study of the conservation of M.HpyAXII MTase activity uncovered the occasional replacement of the HpyAXII R-M system with an alternate gene that we re-annotate as hrgC (HpyAXII replacing gene C). Other H. pylori R--M systems encoding the two most highly conserved MTases M.HpyAI and M.HpyAIII are similarly replaced with genes of unknown function. In the HpyAIII R--M system, gene hrgA inactivated the REase R.HpyAIII in 33% of the 208 strains analyzed but rarely inactivated M.HpyAIII function ([@B54]). hrgA encodes a 370 amino acid protein of unknown function and this gene was associated with gastric cancer in H. pylori isolates from Asian patients but not among Western strains ([@B55]). In the HpyAI R--M system, the REase encoded by iceA1 was replaced with iceA2 in 44% of the strains analyzed ([@B56]). iceA2 (renamed hrgB) encodes a polymorphic protein of unknown function ranging from 24 to 59 amino acid long depending on the strain studied, and epidemiological studies have correlated the presence of gene iceA1 in H. pylori strains with the incidence of peptidic ulcers disease ([@B57]). In our study, we showed that similarly to hrgA and hrgB, hrgC encodes a protein of unknown function but its origin could be traced to a different locus in H. acinonychis sheeba and H. pylori strain NSH57 (G27). Unlike hrgA and hrgB, hrgC replacement always compromised both the MTase and REase activities in our analysis of 37 clinical isolates. Further work will define whether hrgC has any role in H. pylori pathogenicity. As predicted for a type II R--M system, we showed that deletion of gene hpyAXIIM is lethal in the presence of an active R.HpyAXII endonuclease. The lethal phenotype R+M− can be rescued by adaptive mutations, in the form of gene amplification of hpyAXIIM and null mutations in the promoter region of hpyAXIIR. This result is reminiscent of extensive research describing stress-induced mutations in E. coli with the Lac assay system ([@B58]). Based on these findings, we suggest that these adaptive mutations preexisted in the H. pylori population and were selected for as a result of hpyAXIIM deletion. Tandem amplification was previously documented for R--M systems, as when the entire BamHI R--M system was deleted from Bacillus subtilis ([@B38]). In another study, large-scale genomic rearrangements were demonstrated when the PaeR71 R--M system was deleted from E. coli ([@B39]). These rearrangements involved recombination between copies of the transposon IS3 and were proposed to have resulted from multiple rounds of unequal crossing-over or rolling circle amplification. Our study of the deletion of the MTase gene in the HpyAXII R-M system is the first to demonstrate the occurrence of compensatory mutations in the promoter of the respective REase gene. Orthologs of M.HpyAXII generally show poor sequence homology except for one gene of unknown function from Campylobacter upsaliensis RM3195 (CUP1644) that shows 43% identity with M.HpyAXII. Other adenine MTase that target GTAC sites such as M. PabI from Pyroccoccus abyssi and M.CviQI from Chlorella virus only show 14.6% and 17.8% protein identity, respectively. M.RsaI (7.9% protein identity) from Rhodopseudomonas sphaeroides and M.MjaV from Methanococcus janaschii (12.7% protein identity) act on the same sequence but methylates cytosines (m4C). GTAC sites are strongly avoided from the genomes of R. sphaeroides and M. jannashi but not from P. abyssi, suggesting that the PabI R--M system invaded this organism recently as discussed previously ([@B35],[@B59]). The crystal structure of the endonuclease R.PabI was recently solved and unveiled a novel protein fold termed 'half-pipe' ([@B40]). Although the two isochizomers R.PabI and R.HpyAXII show relatively weak sequence identity (25.4%), several conserved motifs are shared between the two proteins ([Figure 5](#F5){ref-type="fig"}B). The R.HpyAXII polypeptide could be threaded with high confidence onto the tertiary structure of R.PabI (PHYRE, E-value 3e-26, [Figure 5](#F5){ref-type="fig"}C) suggesting that R.HpyAXII folds into a similar half-pipe structure. Among the thousands of confirmed and hypothetical REase enzymes identified, Orlowski and Bujnicki predicted that only eight present the half-pipe fold ([@B60]). R.HpyAXII therefore constitutes an excellent candidate for refined biochemical analyses that will enrich our understanding of this new class of enzymes. SUPPLEMENTARY DATA ================== [Supplementary Data](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1) are available at NAR Online. FUNDING ======= National Institutes of Health (AI054423 and DK53708 to N.R.S., AI55396 to O.H.). Funding for open access charges: National Institutes of Health (AI054423). Conflict of interest statement. The project\'s contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH. Supplementary Material ====================== ###### \[Supplementary Data\] We thank Marion Dorer for critical reading of the article, Laura Sycuro for generating the catsacB cassette, New England Biolabs for providing the m6A antibodies and Barry Stoddard for helpful discussions. [^1]: ^a^Based on 26695 annotation ([@B61]). [^2]: ^b^The number of conserved sites is given when higher than one. The exact position of the site is given only when within 200bp from the start codon of a gene. [^3]: ^a^Donor plasmid pTM113-cat contains a total of five GTAC sites and was constructed by substituting cat for aphA3 in pTM113 ([Supplementary Table S3](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)). pTM113-cat was isolated from H. pylori strain NSH57 wild-type (M+) or NSH57hpyAXIIM^N87A^ (M−). A total of 3.3 ng of plasmid DNA was used for each transformation. [^4]: ^b^Transformation frequency was calculated by dividing the number of transformants recovered by the total number of recipient bacteria and was based on the average of three replicates. [^5]: ^c^Strain NSH57hpyAXII~HPAG1~ (R+) encodes an active R.HpyAXII and strain NSH57hpyAXIIM/R~HPAG1~ ΔhpyAXIIR::aphA3 (R−) lacks this enzyme. [^6]: ^a^Donor genomic DNA was constructed by inserting the aphA3 cassette at position 2586bp (from start codon) in one of the two copies of 23S rDNA genes. One GTAC site is present in aphA3 at position \#94 bp and three flanking GTAC sites are found in close proximity to the marker at positions \#2527, \#2660 and \#2745. Chromosomal DNA was isolated from H. pylori strain NSH57 wild-type (M+) or NSH57ΔhpyAXIIM::cat (M−), and predigested or not with RsaI. A total of 10 ng genomic DNA per tranformation was used for M− and 7.9 ng for M+. [^7]: ^b^Transformation frequency was based on the average of three replicates. [^8]: ^c^Strain NSH57hpyAXIIM/R~HPAG1~ (R+) encodes an active R.HpyAXII and strain NSH57hpyAXIIM/R~NSH57~ (R−) encodes an inactive enzyme. [^9]: ^d^Ratio is infinite because no transformants were recovered for R+ recipient strain [^10]: ^a^NSH57 wild-type genomic DNA was constructed by replacing the entire HpyAXII R-M system with the catsacB marker. 500ng genomic DNA per transformation was used. [^11]: ^b^A PCR product was engineered to disrupt genes hpyAXIIM or HP0368. The 5′ and 3′ homologous ends of the respective gene was fused to the antibiotic resistance cassette and transformed to generate a null allele by allelic replacement. A 150ng DNA per transformation was used for ΔhpyAXIIM::cat and ΔHP0368::cat. [^12]: ^c^Transformation efficiency was based on the average of three replicates. [^13]: ^d^As in [Table 2](#T2){ref-type="table"}. [^14]: ^e^A total of two clones was recovered. 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Q: Class Inheritance and Casting So I was given this code in a folder of bits and pieces that were to be for a project which has since halted development. However, being new to Java there are several questions I have (and I'm aware the code does not compile, but that works into one of my questions). interface Executable { public int execute (Object o); } public class Biv implements Executable { public int execute (String s) { System.out.println (s); return s.length(); } public static void main (String[] args) { Executable e = new Biv(); System.out.println( e.execute ("Hello World!")); } } 1) My first question is to do with the variable e. It is declared with the Executable object type, however I don't understand why it can then be instantiated with a new Biv object. What is going on here, what does it mean? 2) The error is in the execute method within the Biv class. This seems to be because it expects an object rather than a String. However, can you not replace a Object with a String because String is a subclass of Object? I could understand if you replaced String with Object it would have an error (I think) but not how it is currently done. A: I don't understand why it can then be instantiated with a new Biv object Because Biv implements Executable, so any instance of Biv is also an instance of Executable. The error is in the execute method within the Biv class Yes it is, it [Biv] does not implement execute(Object). The method execute(String) is just a different method that happen to have the same name, since they don't have the same signature. Any class that implements the interface Executable must override the method execute(Object). There is no co-variance of arguments in java for overriding methods, because it will be unsafe. What if you invoked e.execute(new Object())? 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Inside every living cell are molecule-building factories called ribosomes. These tiny machines read blueprints of genetic information and fabricate the molecules that make up all life. They are hugely important to genetic engineers and researchers, because controlling ribosomes could be the way to synthesize the custom-made biological nano-machines of the future—ones that could make anything from therapeutic human antibodies to the next generation of unfathomably complex super-materials. There's a problem: Engineering a ribosome to do interesting tricks often means paralyzing and killing its parent cell. But today, a team of biologists and biological engineers at Northwestern University and the University of Illinois have made a fascinating breakthrough that could help scientists get around this roadblock. As they report in a new study in the journal Nature, the scientists have created unique, experimental ribosomes they're calling Ribo-T that are the first ever to passively co-exist with a living cell's natural ribosomes. It means that for the first time, researchers will be able to tinker with ribosomes in living organisms, such as bacteria, without worrying about killing the lifeforms they're studying. "You can think of it like this: Imagine you only have one family car and you want to start modifying it, say, putting a truck bed in," says Alexander Mankin, a biologist with the team at the University of Illinois. "With each modification, you risk breaking down important processes, like losing the back seat your kids need. This is the same with these ribosomes. But here, [having Ribo-T] is a bit like having two cars, instead of one." So you can modify Ribo-T in any way you want without worrying about destroying the whole setup, he says. The genetic lasso What makes ribosomes so hard to work with is their fundamentally weird nature. Here's an oversimplification of the strange setup: In all living cells, ribosomes are broken up into two independently floating parts. There's a smaller "reader" half of a ribosome, which attaches to a strip of genetic data, and a larger half that assembles the molecules. Each cell is a sea of ribosomes halves. Those halves randomly join together to read and create a molecule, then split up and promiscuously recouple with totally different halves. Based on what we know about cell biology, this really shouldn't have worked. According to Mankin, that two-parted nature has made genetically engineering these molecules machines almost impossible. You either genetically engineer the whole sea, or nothing at all. But Mankin and his fellow scientists had an idea, one that totally went against what scientists thought they understood about ribosomes. Why not just tie the two halves of certain ribosomes together indefinitely? Based on what we know about cell biology, this really shouldn't have worked. The reason is that the two ribosome halves need to move around relative to each other as they built molecules, which a tether might prevent. Researchers also didn't know how such a tied-together ribosome would find the strips of genetic data blueprints it reads. For the most part, it didn't work. Mankin and his colleagues tried to tie the ribosome halves together tethers of basically nonsense sticky RNA. They tried 91 different combinations, and most of them failed. A few of them worked, albeit it very poorly. But here's where the team did something really clever: They let a cutthroat competition decide which tether was best. By joining the RNA of the large and small ribosomal subunits into a unique chimaeric molecule, it was possible to engineer functional ribosome with tethered ribosomal subunits (Ribo-T) Eric Carlson The researchers were thinking that the length of the tethers might impact how well the combined ribosomes were able to function, since the ribosome halves need to shift around without breaking their connection. So Mankin and his team genetically engineered a handful of bacteria with tied-together ribosomes, each with different tether lengths. Then the scientists let them compete on a petri dish with limited food for two days to see which bacteria out-competed the rest. "This way the cells told us themselves what was the best ribosome tether design in the smorgasbord of options we offered," he says. In the end, bacteria with two sticky tethers 8 and 9 RNA nucleotides long was the champion. Having found the optimal length, the scientists did one last round of bacterial gladiator battle to se whether—with enough time—some bacteria might spontaneously evolve some trait that would make the combined ribosomes more efficient. "After several dozens of generations, a bacteria did," Mankin says, and it dominated a different petri dish with more gusto than any other strain. (Exactly why this random mutation allowed a bacterial with a combined ribosome to grow faster is still a mystery, he says.) Scaffolds for the science of the future "The answers to these questions will illuminate the basic mechanisms of molecule creation." Finally, Mankin and his team had created a combined and tethered ribosome that works surprisingly well: Ribo-T. A bacterial cell using only Ribo-T ribosomes will grow normally, but at about 45 percent the speed of a non-engineered cell. Joseph Puglisi, a biologist at Stanford University who was not involved with the project, says that figure is actually damned impressive. In an essay accompanying the Nature paper, Puglisi confirms that Ribo-T, while a bit slower, can create any of the molecules a normal ribosome can make. That makes Ribo-T—which can be genetically created to appear alongside a population of normal, halved ribosomes—the perfect scaffold for a new wave of genetic engineering experiments. Better still, Puglisi says, because we now have the first platform where we can test and tinker with truly delicate and crucial ribosomal features (without worrying about killing our experiment), Ribo-T may offer new insights into the mysterious inner-workings of the ribosome—which, as Mankin admits, is still poorly understood. We can now ask basic questions like why ribosomes seem unable to create certain types of molecules. "The answers to these questions will illuminate the basic mechanisms [of molecule creation] and will probably cause surprise," Puglisi says. "Armed with this knowledge, thoughtful engineers will continue to tinker with the ribosome. This content is created and maintained by a third party, and imported onto this page to help users provide their email addresses. 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[Diet and lifesyle of a cohort of primary school children]. The obesity is the disease of the new millennium, because it affects about 300 million people in the world, and especially it has a high prevalence in children. Obesity is a significant risk factor for cardiovascular disease, diabetes mellitus type II, hypertension, problems of adaptation and relationship with other, lower self-esteem and depression. The objective of our study is to identify children at risk of overweight/obesity in order to primary prevention. We have organized meetings with children, families and school's members where we discussed the results of our investigation about the importance of healthy diet and lifestyle. The study was carried out on 545 children (282F, 263M), age 6.-10 years, of two primary schools in Catanzaro, from 2008 to 2010. The valuation parameters were: gender, age, weight, height, blood pressure and waist circumference. To children were also administered a questionnaire about dietary habits and lifestyle. Fisher's test. We had that 62% of children was normal weight, 27% overweight, 11% obese. A particularly relevant datum is that the percentage of overweight-obese boys of 8 and 9 years old was higher (56%) than that of normal weight. We found cases of hypertension only in obese children. 98% of obese, 80% of overweight and 24% of normal weight children had a high waist circumference. We did not find differences in food quality among normal weight and overweight/obese children. Instead, we found significant differences in behavior between children: 90% of obese, 64% of overweight and 53% of normal weight children passed more than 2 hours in the afternoon watching television, playing computer and video games. 70% of normal weight, 82% of overweight and 95% of obese children practiced physical activity. Our study shows a alarming fact about the increase of the obesity in children. In particular the most important problem is that this condition could predispose to cardio-metabolic, endocrine, respiratory, musculoskeletal and psychological consequence. So it is important that everybody who lives with children, especially parents and school's members, educates children to have healthy lifestyles. These attentions may slow the worryng epidemic of obesity.	3.34375	3	[ 0.00116729736328125, -0.000732421875, -0.006072998046875, 0.0230712890625, -0.01116943359375, -0.0038909912109375, -0.0004119873046875, -0.01104736328125, 0.00946044921875, -0.00018596649169921875, 0.0037078857421875, 0.023681640625, -0.005462646484375, 0.0032806396484375, -0.010498046875, 0.00015354156494140625, 0.01141357421875, 0.0062255859375, -0.005279541015625, -0.0026397705078125, 0.01171875, 0.005828857421875, -0.01318359375, 0.005126953125, -0.0029754638671875, -0.0033416748046875, -0.0036773681640625, -0.01318359375, 0.011962890625, -0.0004100799560546875, 0.01422119140625, -0.0189208984375, -0.034912109375, -0.030517578125, -0.000888824462890625, -0.007598876953125, 0.004364013671875, -0.006011962890625, -0.0025177001953125, 0.061767578125, -0.00531005859375, -0.007781982421875, 0.00482177734375, -0.0093994140625, -0.006866455078125, -0.01556396484375, -0.01708984375, 0.016845703125, 0.0017852783203125, 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Look at the science behind the prevention method To find a cancer prevention method with a proven track record, look at how the method was tested. The way tests are set up can affect the outcome, and sometimes can make it look like a method or substance prevents cancer when it really doesn’t. Pre-clinical tests Studies in cells (laboratory studies) Scientists usually start by testing a new prevention method or treatment on cells in a dish in the lab, to find out if it has any effect there. They may treat cells with a known cancer-causing agent and then add the compound they’re testing to see if it stops pre-cancerous changes in the cells. If it doesn’t, they may change the formula or use different types of cells to try it again. Sometimes studies like this show some effect on the cells, and they’re published. News broadcasters may then treat the study as proof that a cancer prevention method works. But just because a compound stops abnormal cell growth when it’s added to cells in a lab dish does not mean that it will work in the human body. This means that if you're looking at a report of a research study – even one that says a treatment “stops the growth of cancer cells” – you may notice that there’s no mention of people. Some of these lab studies use human cancer cells, but others use cancer cells from animals. (Either way, studies done on cells alone are called in vitro studies.) At this point, anything that stops cancer cells may sound like good news. But there are many compounds that can keep cancer cells from growing in a lab dish that don’t work or aren’t safe in people. Some reasons a treatment might not work for people is that the substance also hurts or kills normal cells, or because the body can’t absorb it and get it to the place where it’s needed to stop cancer. Sometimes, even if the substance can be absorbed, can reach all the body tissues, and doesn’t harm normal cells, the amount of the substance that gets to the tissues isn’t enough to stop the cancer cells. There are many hurdles between lab studies and human ones. Studies in animals If the researchers find the effect they want in cells in a dish, they may move on to animal tests. This can help them find out if the substance can be absorbed from the stomach or intestine, and learn how it’s distributed in the animal’s body. They may look for good and bad effects. Because some of these reports are published, you may also hear about them on the news. These are called in vivo studies. This means that they were studied in living creatures. If the study was done in animals, good outcomes may sound promising. But methods that work in animals don’t always work when they are tested on people. Animal studies often help scientists know which drugs may be toxic to people, and which may have unexpected effects. Sometimes a drug or food supplement turns out to do almost the exact same things in people as animals, but many don’t work for one or the other. And as any veterinarian can tell you, some foods and drugs that are safe for animals can hurt people, and some foods and drugs that are safe for people can hurt animals. So while animal tests can give researchers certain types of valuable information, they still may not show how the compound will affect people. News stories on lab and animal studies can mislead In both lab studies and animal studies, the research report may be published. Usually, the researcher’s own report makes it clear that more studies need to be done to see if the substance makes a difference in people. But if a news group picks up the story and publishes it, they may not mention how the study was done or that more study is needed. Often the headlines, and sometimes even the full story, do not clearly say what kind of study was done. Sometimes the news reports on this very early research may make it sound like the method will work in people, which can lead to confusion. This is why it helps to look at the whole printed story, and then see if you can find out more about the details of the research. Always keep in mind that there’s a huge difference between positive results in lab or animal studies and good results in human studies. Select A Hope Lodge Please share your thoughts about your cancer.org website experience. If you need immediate cancer-related information or patient program assistance, please call 800-227-2345 any time day or night. Email Address (optional) Praise Dislike Suggestion What made your cancer.org website experience great?What made your cancer.org website experience challenging? 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Clothing during the early part of the 19 th century consisted of simple lines and bright, Oriental inspired colors. But, by mid century, widespread use of the sewing machine started a revolution in clothing akin to the industrial revolution that brought it to the forefront. The stronger stitches and faster methods presented the possibility for more intricate details and trim. The poorer class still sewed the clothing by hand. But, for those with the means, Victorian clothing began to take on the fussy characteristics that we commonly associate with the era. Womens Clothing For women, dressing was all about layers…and layer, and layers. It was typical to find, from the inside to the outside: Lace trimmed drawers made of cotton or linen A corset with boning to provide structure A camisole to cover the corset A hoop skirt Stockings attached to garters Petticoat(s) A very full skirt, some dresses for daytime even had a train A bodice, with additional boning, that fastened in the front Some kind of outer garment, such as a shawl Mitts or gloves Boots with button closures A hat or bonnet to cover the head Numerous accessories like handkerchiefs and fans All of the pieces would have been made from rich fabrics accented with elaborate twists, tucks, and trims. Women had special dresses for everything from mourning, to ball gowns, to outdoor recreation. The improved railway system made travel more efficient. It was fashionable to spend weekends “in the country” for recreation. The multiple activities meant that women spent much of their weekend changing their clothing. Mens Clothing Prosperity afforded more leisure time and men’s clothing began to reflect a more casual lifestyle. Drab knickers and fitted coat tails gave way to more colorful fabrics and flowing lines. Coats were longer and fuller and echoed the small waist silhouette of women’s clothing. As the era progressed, it became common to see men with colorful scarves or ascots. The Victorian fussiness was also apparent by the addition of scarf pins, cuff links, and heavy watch chains crossing the waist to a pocket. Men carried canes with intricate carvings and silver knobs. As the Victorian era neared its end, men were seen carrying accessories used for cigar smoking. And, in a trend that would last until the middle of the next century, men sported the single lens monocle associated with an English dude. Later Victorian Clothing It is no surprise that the approach of the 20th century found Victorians weary with all of the detail. Late Victorian clothing was becoming simpler with more muted colors. 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MAVEN's top 10 discoveries at Mars MAVEN spacecraft and the limb of Mars. Credit: NASA's Goddard Space Flight Center On June 17, NASA's MAVEN (Mars Atmosphere and Volatile Evolution Mission) will celebrate 1,000 Earth days in orbit around the Red Planet. Since its launch in November 2013 and its orbit insertion in September 2014, MAVEN has been exploring the upper atmosphere of Mars. MAVEN is bringing insight to how the sun stripped Mars of most of its atmosphere, turning a planet once possibly habitable to microbial life into a barren desert world. "MAVEN has made tremendous discoveries about the Mars upper atmosphere and how it interacts with the sun and the solar wind," said Bruce Jakosky, MAVEN principal investigator from the University of Colorado, Boulder. "These are allowing us to understand not just the behavior of the atmosphere today, but how the atmosphere has changed through time." During its 1,000 days in orbit, MAVEN has made a multitude of exciting discoveries. Here is a countdown of the top 10 discoveries from the mission: 10. Imaging of the distribution of gaseous nitric oxide and ozone in the atmosphere shows complex behavior that was not expected, indicating that there are dynamical processes of exchange of gas between the lower and upper atmosphere that are not understood at present. 9. Some particles from the solar wind are able to penetrate unexpectedly deep into the upper atmosphere, rather than being diverted around the planet by the Martian ionosphere; this penetration is allowed by chemical reactions in the ionosphere that turn the charged particles of the solar wind into neutral atoms that are then able to penetrate deeply. 8. MAVEN made the first direct observations of a layer of metal ions in the Martian ionosphere, resulting from incoming interplanetary dust hitting the atmosphere. This layer is always present, but was enhanced dramatically by the close passage to Mars of Comet Siding Spring in October 2014. 7. MAVEN has identified two new types of aurora, termed "diffuse" and "proton" aurora; unlike how we think of most aurorae on Earth, these aurorae are unrelated to either a global or local magnetic field. 6. These aurorae are caused by an influx of particles from the sun ejected by different types of solar storms. When particles from these storms hit the Martian atmosphere, they also can increase the rate of loss of gas to space, by a factor of ten or more. 5. The interactions between the solar wind and the planet are unexpectedly complex. This results due to the lack of an intrinsic Martian magnetic field and the occurrence of small regions of magnetized crust that can affect the incoming solar wind on local and regional scales. The magnetosphere that results from the interactions varies on short timescales and is remarkably "lumpy" as a result. 4. MAVEN observed the full seasonal variation of hydrogen in the upper atmosphere, confirming that it varies by a factor of 10 throughout the year. The source of the hydrogen ultimately is water in the lower atmosphere, broken apart into hydrogen and oxygen by sunlight. This variation is unexpected and, as yet, not well understood. 3. MAVEN has used measurements of the isotopes in the upper atmosphere (atoms of the same composition but having different mass) to determine how much gas has been lost through time. These measurements suggest that 2/3 or more of the gas has been lost to space. 2. MAVEN has measured the rate at which the sun and the solar wind are stripping gas from the top of the atmosphere to space today, along with the details of the removal processes. Extrapolation of the loss rates into the ancient past—when the solar ultraviolet light and the solar wind were more intense—indicates that large amounts of gas have been lost to space through time. 1. The Mars atmosphere has been stripped away by the sun and the solar wind over time, changing the climate from a warmer and wetter environment early in history to the cold, dry climate that we see today. "We're excited that MAVEN is continuing its observations," said Gina DiBraccio, MAVEN project scientist from NASA's Goddard Space Flight Center in Greenbelt, Maryland. "It's now observing a second Martian year, and looking at the ways that the seasonal cycles and the solar cycle affect the system." MAVEN began its primary science mission on November 2014, and is the first spacecraft dedicated to understanding Mars' upper atmosphere. The goal of the mission is to determine the role that loss of atmospheric gas to space played in changing the Martian climate through time. 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1. Introduction {#sec1} =============== The microbiomes, including bacteria, fungi, and viruses, live within and upon all organisms and have become a growing area of research. With the advances of new technologies it is now possible to entangle complex microbial communities found across animal kingdoms. Recent advances in molecular biology have provided new possibilities to investigate complex microbial communities and it has become clear that the vast majority of bacteria living in/on other animals cannot be cultured. It is now commonly accepted that at least 80% of the total bacterial species in the human gut cannot yet be cultured \[[@B1], [@B2]\]. High-throughput DNA sequencing approaches provide an attractive and cost-effective approach to investigate the composition and functions of the host microbiome. The culture-independent analysis of the host microbiome can be obtained by either metagenomic approaches or amplicon sequencing using specific marker genes. Amplicon sequencing provides a targeted version of metagenomics with a specific genetic region shared by the community members of interest. The amplified fragments derive from universal primers and are usually assumed to produce sequence read abundance that reflects the genetic diversity in the studied sample and hence sequence read abundance should reflect the genetic diversity in the studied sample. The amplified fragment typically contains phylogenetic or functional information, such as the 16S ribosomal RNA gene. 16S rRNA gene sequences are well studied and provide excellent tools for microbial community analysis \[[@B3]\], but other functional marker genes can also be used \[[@B4]\]. Subsequent taxonomy profiling of the entire microbial communities is conducted by comparisons to reference sequences or byde novoclustering of specific regions of sequences. Functional profiling of metagenomics is more challenging since major parts of the metagenomic data remain insufficiently characterized and frequently samples are contaminated by host DNA or traces from the diet. Compared to both culture-dependent and more traditional molecular approaches such as sequencing of clone libraries and DGGE, amplicon sequencing approaches allow a more in depth analysis of the complete microbiome and are less restricted to the number of samples to be investigated. For further technical details see, for example, Caporaso et al. \[[@B3]\]. 2. The Microbiome of Animals {#sec2} ============================ The Human Microbiome Project (HMP) \[[@B1]\] was initiated in 2007 and with this it has become clear that the human microbiome is highly diverse and complex. The number of microorganisms sharing the human body is thought to outnumber human cell numbers by a factor of ten and the combined microbiome usually contains 100x more genes than its host. The microbiome also plays a major role in human health \[[@B5]\] and both composition and alterations in the microbiome have been found associated with diabetes, inflammatory bowel disease, obesity, asthma, rheumatoid arthritis, and susceptibility to infections \[[@B10]--[@B11]\]. In recent years the microbiome of a number of vertebrate nonhuman species has been sequenced including livestock \[[@B12], [@B13]\] and wildlife species such as the Tasmanian devil \[[@B14]\], red panda \[[@B15]\], giant panda \[[@B16]\], black howler monkey \[[@B17]\], and koala \[[@B18]\]. Insects are the most diverse and abundant groups of animals on earth \[[@B19]\] and have colonized many different habitats. It is therefore not surprising that insect species are also inhabited by large and diverse microbial communities playing a pivotal role for insect biology. Many insect species are inhabited by a large and diverse assembly of microorganisms, where especially the microbial communities in the intestinal tract have received much attention \[[@B20]--[@B21]\]. Some insect species show a much more diverse microbiome compared to other insect species. For example, the microbiomes of some synanthropic flies, such as the green bottle fly, show high diversity compared to other species such as fruit flies or mosquitoes \[[@B25]--[@B23]\]. The high species richness could reflect the lifestyle of synanthropic flies, for example, breeding and living by animal manure, bedding, and/or decaying organic matter rich in microorganisms. The microbiome of other groups of invertebrates has also been established although for a limited number of species. Studies have compared the microbiome of different species of marine invertebrates with or without photosynthetic symbionts including five families of marine invertebrates \[[@B26]\]. Marine species of commercial interest such as oysters have also been addressed \[[@B27]\]. The microbes of soil invertebrates have received some attention. The gut microbes of soil animals play an indispensable role in the digestion of food and are of ecological importance in the global carbon cycle. Recently, research reported that like that of terrestrial insects some soil invertebrates such as collembolans, earthworms, and nematodes contain a rich microbiome and putative symbionts \[[@B29]--[@B30]\]. Further, results have shown how differences in diet among earthworm ecological groups lead to the establishment of different bacterial communities \[[@B29]\]. Moreover, perturbation of the soil ecosystem could impact earthworm gut wall-associated bacterial community composition and hence earthworm ecology and functioning. Even though the microbial community in invertebrates like that of collembolans and earthworms is not fully addressed, there is convincing evidence that intestinal communities can contribute to the degradation of recalcitrant biological materials such as chitin and lignocellulose \[[@B29], [@B28], [@B31]\]. 3. Factors Affecting the Animal Microbiome and the Biological Significance {#sec3} ========================================================================== To begin with all microorganisms were seen as pathogens causing infectious diseases to the host. The host immune system of eukaryotes was built to eliminate these intruders, but at the same time tolerating its own molecules. However, we now know that the association between eukaryotic hosts and the microorganisms is far more complex. With the advances in molecular biology, such as next generation sequencing, it is now possible more specifically to address the association between a host and its microbiome. In animals the association between the host and its microbiome can take many forms and includes symbiotic and pathogenic associations \[[@B20]\]. Symbiotic microbiomes can be beneficial to the hosts in many ways, including dietary supplementation, host immune system, and social interactions \[[@B22], [@B32]\]. In many insects, the gut symbionts are essential for survival and development and suggest the presence of a core microbiome \[[@B33]\]. The symbionts need not to be completely dependent on the host and animal-microbial interactions can be flexible and facultative and the host can carry different symbionts at different times \[[@B20]\]. The association between the host and the microbiome is also affected by a large number of abiotic and biotic factors and can involve the immune system, nutrition, reproduction, communication, and many other systems of the host \[[@B2], [@B34]--[@B36]\]. The number of studies addressing the role of the microbiome on animal health is limited and almost entirely restricted to human studies. However, a large number of studies have addressed the role of single bacterial symbionts on animal fitness, where especially insect species have received much attention \[[@B39]--[@B38]\]. There is now a growing interest in understanding what factors can affect the microbiome of animals in order to understand how fitness is affected and to explain differences between ecosystems, species, and/or populations. The composition of the bacterial communities of animals including invertebrates and vertebrates seems to be shaped by multiple factors, such as the host genotype \[[@B21], [@B25], [@B40], [@B41]\], diet \[[@B17], [@B34], [@B39], [@B42]\], life stage \[[@B43]\], laboratory rearing \[[@B34], [@B43], [@B44]\], and the ecological and physiological conditions of, for example, the gut of the insect \[[@B21]\]. Further, recent studies have proposed that the microbiome impacts the nutritional supplementation, tolerance to environmental perturbations, and maintenance and/or development of the immune system \[[@B20]\]. Some invertebrates lack the complexity and diversity of associations with microorganisms. Such insect model systems allow investigations that aim to understand the contribution of specific bacteria and the entire microbiome towards host physiological processes. For example,Drosophila melanogaster provide a promising model system to address some of these issues and for this species it is possible to rear axenic flies. Next generation sequencing approaches can provide an in-depth analysis of the functional roles of specific groups of bacteria and the entire microbiome on the fitness of the host. Results onD. melanogaster have shown how the microbiota affects developmental rate and changes metabolic rates and carbohydrate allocation under laboratory conditions \[[@B32]\]. Similarly functional analysis of the microbiome of ants also suggests large capacity to degrade cellulose \[[@B45]\] and that metabolic functions of microbes in herbivorous species play a role in fixing, recycling, or upgrading nitrogen \[[@B46]\]. Hypothesis has also been proposed to describe that gut microbiomes might facilitate insect herbivory and that variation in the ability to consume chemically defended plants can be partly explained by variation in the gut microbiome \[[@B47]\]. Recent studies have highlighted the importance of the microbiome not only in shaping the immune system but also in the context of host pathogen transmission processes (for reviews see \[[@B20], [@B48]\]). An example hereof is that the success of malaria infections is not only influenced by the mosquito innate immune responses and genetics but also affected by the composition of the gut microbiota and is in fact one of the major components affecting the outcome of mosquito infections \[[@B24]\]. Studies have also suggested that abiotic factors can affect the microbiome of disease vectors and thus vector competence of the host \[[@B23], [@B35]\]. Similarly the epidemics of human pathogens transmitted by insect vectors correlate with environmental factors \[[@B49], [@B50]\] suggesting that the vector competence of insect vectors is affected both indirectly and directly by environmental factors \[[@B35], [@B51], [@B52]\]. The recent interest in the importance of the microbiome on tolerance to environmental perturbations \[[@B37], [@B38]\] has revealed the presence of single bacterial species and mainly endosymbionts with large impact on, for example, temperature tolerance (for review see \[[@B38]\]). Temperature can affect the host directly or indirectly through either abundance of the symbiont or efficiency of transmission to the offspring \[[@B53]--[@B55]\]. At present it is unclear to what degree single strains of bacteria play a dominant role in tolerance to environmental factors or if interactions between bacteria of the microbiome are dominant. The recent advances in molecular biology and implementation of statistical analysis allow more specific hypothesis to be tested on effects of the microbiome on tolerance to, for example, environmental stress. 4. Conservation and Implications for Conservation {#sec4} ================================================= Changes in the microbial community have been shown to affect fitness of humans and other species as described above. However, the implications of changes in the microbiome for animal conservation have only been addressed in a limited number of studies even though the implications are many. Several studies using next generation sequencing approaches have addressed the comparison of the microbiome of laboratory populations or individuals kept in captivity with that of wild animals \[[@B14], [@B15], [@B18], [@B34], [@B44]\] or of single species in habitats influenced by different degrees of human behavior \[[@B17]\]. Results show that species across taxa living under laboratory conditions or affected by habitat fragmentation show less diverse microbiomes compared to wild species. Thus species are jeopardized not only directly by degraded habitats with reduced resource availability but also indirectly through diminished microbiomes. It is thus essential that future studies address the microbiome and how habitat fragmentation impacts the microbiome in different species and how species with less diverse microbiomes perform under these conditions. It is essential that we address the importance of the microbiome of other species rather than humans and the impact it has on their health status. For larger species such as primates this can be difficult and often only correlative evidence exists or can be achieved through a functional annotation of the microbiome \[[@B14], [@B17]\]. For example, in a study by Amato and coworkers \[[@B17]\] it was shown that beneficial fermenters, acetogens, and methanogen bacteria were more abundant in black howler monkeys inhabiting evergreen rainforest compared to individuals from fragmented habitats. The latter group also contained higher numbers of sulfate-reducing bacteria producing undesirable end products such as H~2~S. This strongly suggests that habitat fragmentation will affect not only the microbiome of the host but also host fitness. Similarly, keeping animals under captivity and maintaining breeding populations are likely to affect animal microbiomes. This is often undertaken in order to protect or increase abundance of rare species aiming at releasing species into the wild again. However, if the microbiomes of the individuals being released are affected, this is likely also to affect fitness compared to that of wild individuals and will subsequently reduce the probability of successful reintroduction into the wild. This is supported by studies on humans and mice where results have shown that obesity causes shifts in gut microbiome composition \[[@B10], [@B56]\]. Similar nutritional conditions could be expected for individuals kept in captivity. Molecular approaches allow researchers to establish entire microbiomes of animals and thus also test if, for example, it is possible to acclimate animals before being released into the wild. Optimizing environmental conditions of species in captivity could potentially ensure successful management and reintroduction. It has been suggested that engineering microbiomes can be used to improve plant and animal health \[[@B57]\]. How this can be incorporated into conservation is unclear. It is standard to employ basic principles of genetics into breeding strategies for endangered species in zoos or captivity, but the microbiomes evolutionary potential has been ignored also in conservation biology. Inbreeding has been suggested to affect the demography and persistence of natural populations and play an important role in conservation biology \[[@B58]\]. Recent work shows that inbreeding depression in bird and mammal populations significantly affects birth weight, survival, reproduction, and resistance to disease, predation, and environmental stress \[[@B59]\]. Inbreeding depression is expected to change the proportions of homozygotes and thus also heterozygotes. Consequently recessive deleterious mutations are likely to be expressed. As fitness of animal populations is expected to be affected by genotype of the host and the microbiome and interaction between the two it is also likely that the microbiome will be affected by inbreeding depression either directly or through interaction with the genotype of the host, not only because the genepool is diminished but also because of a compromised immune system. Microbiome analysis of wild populations has shown that the microbiome is dependent on the surrounding habitats as discussed above. This information might be used as a sensitive screening tool to establish populations affected by habitat fragmentation \[[@B17]\] and possibly also the effect of inbreeding. The strong signal from the diet \[[@B17], [@B34], [@B39], [@B42]\] suggests that the microbiome can also be used as a screening tool of diet preferences and to protect critical food resources or habitats for endangered species. However, it is essential that we fully understand the temporal and spatial changes in the microbiome if we are to use it as a screening tool. The microbiome can provide protection of the host from pathogens either through stimulation of the immune system or through competitive exclusion. However, when animals are compromised or exposed to unfavorable environmental conditions the symbionts themselves can act as opportunistic pathogens \[[@B2], [@B27]\] or not provide the same degree of protection. There are examples of how environmental conditions can affect the microbiome of invertebrates. For example, studies have shown how changes in temperature have caused shifts from mutualistic to pathogen dominated communities in corals \[[@B60]\]. In oysters temperatures over 20°C can cause summer mortalities, but temperatures as low as 14°C will promote development of brown ring disease in clams \[[@B61], [@B62]\]. This is important in conservation biology given the fact that species and populations are or will be exposed to changes in climate under the future climate scenarios. Host species will thus be exposed to not only the direct effects of changes in, for example, temperature but also indirect effects due to change in abundance or species composition of the microbiome. These changes can again lead to direct fitness effects on the host or indirect effects through changes or modification of the immune response. The microbiome could potentially also allow organisms to respond on a short timescale and cope with, for example, changes in climate. In particular, for species with a long generation time populations might not be able to adapt to fast changes in climate. However, bacteria with a short generation time can adapt on a shorter timescale compared to the host and may provide fitness advantages that allow the host to cope with changes in climate. Future studies should more specifically test if and how the microbiome affects animals ability to respond to a changing environment. Such plastic responses can have important implications for persistence of species or populations at risk in a fluctuating environment. Differences in microbiomes may affect invasions. For example, the interactions between native and nonnative of closely related species may be affected by the transmission of bacteria. This also appears to be associated with another emerging type of invasion, the transmission of infectious diseases of wild animals to humans \[[@B63]\]. Such transmission may be associated with factors including changes in human and nonhuman microbiomes. These interactions also have important implications for the conservation and management of different species within the environment. Some studies have addressed the microbiome of invasive species and also compared populations originating from the species native region with that of invasive regions \[[@B64], [@B65]\]. For the invasive snail,Achatina fulicaresults showed a highly diverse microbiome and functional analysis revealed a variety of microbial genes encoding enzymes, which is in agreement with the wide-ranging diet of this species \[[@B65]\]. Interestingly in another study comparing the microbiome of the soybean aphid,Aphis glycines from populations of native and invasive regions showed no differences \[[@B64]\]. Future studies should address the importance of the microbiome of invasive species to investigate if single strains of bacteria, the entire microbiome, or their interactions are major determinants for a species ability to establish in a new environment and if invasive microorganisms carried by introduced species affect native species \[[@B66]\]. 5. Conclusions {#sec5} ============== Recent advances in molecular biology have given new possibilities to establish complex microbial communities and it has become clear that the vast majority of bacteria living in/on other animals cannot be cultured. One of the most common methods to describe complex microbiomes is the sequencing of the bacterial marker 16S ribosomal RNA (16S rRNA) genes through amplicon sequencing. Studies have shown that the microbiome plays a major role in human health, and in recent years the microbiomes of an increasing number of nonhuman species have been investigated. However, the number of studies addressing the role of the microbiome on animal health still remains limited. Some studies have discussed the role of the microbiome on nutritional supplementation, tolerance to environmental perturbations, and maintenance and development of the immune system. Thus the implications of changes in the microbiome for animal conservation are many although a limited number of studies have addressed this. We suggest that a number of factors relevant in conservation biology could affect the microbiome of animals including inbreeding, habitat fragmentation, change in climate, and effect of keeping animals in captivity. Changes in these factors are thus also likely to affect the fitness of the host both directly and indirectly. With the development of next generation sequencing and functional analysis of microbiomes it has become possible more specifically to test direct hypothesis on the importance of the microbiome in conservation biology. This work was supported by the Danish Council for Independent Research (Grant no. 11-116256) (Simon Bahrndorff) and the Aalborg Zoo Conservation Foundation (AZCF). Competing Interests =================== The authors declare that there is no conflict of interests regarding the publication of this paper. 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Coup de la Glotte Intending to encapsulate and codify the technique and style of the singers of the first forty years of the nineteenth century, Manuel Garcia based much of his ‘Treatise on the Art of Singing’ on the practice of his sister and his illustrious father. Within the previous decade both had died unexpectedly and early; his father, Manuel Vicente del Popolo Garcia, at 57 in 1832, and Maria Malibran, his sister, at the unbelievably early age of 28, in 1836. Garcia’s treatise rested on the teachings and method of his father, the teacher of both his son and daughter and whose youngest child, who was later to become Pauline Viardot-Garcia, had already started to play for his lessons by the age of eleven. From this small family came one of the most celebrated of all Rossini tenors – Manuel Garcia the elder; his son, the most influential teacher of all; and two of the century’s most illustrious singers – Malibran and Viardot-Garcia. Garcia senior had trained in Spain and later had studied with Giovanni Anzani, a famous bel canto tenor of the previous generation. So the precepts of the previous century, dominated by the castrati, flowed from his studio. All of the children were taught composition as well as singing, and both daughters followed their father in becoming composers themselves. Manuel Garcia, the younger, seems to have used his compositional talents to write vocal exercises and their accompaniments in his treatise. Part I describes the practice and techniques to become a good singer of the period and Part II, the style and use of the technique in performance. His work was based largely on his father’s and sister’s careers and that of their colleagues and contemporaries during the age of Rossini – the period which has become known as the Age of Bel Canto. Garcia’s attention to detail included not only breathing and other technical essentials, but also a description of the absolute beginning of the sound, known in Italian as attacco and in German as Ansatz. As he wrote in French, the initiation of the sound came out as the coup de la glotte – ‘shock of the glottis’. Poor Garcia! He can never have imagined the trouble and confusion this innocent phrase was to cause him for the rest of his days. During the last two decades of his long life, the vogue among voice teachers turned away from the bel canto precepts on which he had been brought up, and veered towards the new, but mistaken, concept of breath pressure theory. This determined that the vocal cords were activated only by a direct air blast from the lungs. In contrast, the ‘bel cantoists’ held that the tone was started by breath already controlled by the so-called ‘vocal struggle’ – la lotta vocale: the expiratory muscles being opposed by the inspiratory, thus allowing the breath flow at the chords to be controlled from the softest and most gentle tone to the strongest and loudest. Thus, the vocal cords never had to withstand forced air from below and therefore were always capable of vibrating freely and without strain. Because of the breath pressure theories – which continue up to the present day, alas – means were sought to take the strain away from the cords which such a strong air blast placed on them. So the tone was aimed as far away from them as possible: ‘in the ‘masque’; forward; behind the upper teeth; in the sinuses behind the nose; behind the eyes; on to the hard palate; anywhere, provided it was away from the larynx. The fact that vocal tone is generated entirely by the vibrating cords and the resultant sound resonating in the pharynx, was either ignored or disbelieved. The speed of sound (323 mps) was not taken into consideration at all, and the impossibility of aiming sound travelling at such a speed within an instrument only a few inches long was not contemplated. From this time, Garcia’s phrase, coup de la glotte, began to acquire sinister overtones which distorted and quickly anathematized the original meaning. A major element in this was a misunderstanding of the nuances of the French language, as Garcia’s treatise reached English speaking audiences. Coup literally means ‘shock’, ‘blow’, ‘knock’ in English, and is combined with genitive nouns for varied, specialised meanings. For example: coup de bec – peck; coup de tête – head butt; coup de poing – punch; coup de pied – kick; coup de coude – blow with the elbow or nudge; coup d’épée’ – sword thrust; and also more figurative meanings such as: coup de sifflet – whistle blast; coup de téléphone – telephone call; and coup de foudre – thunderbolt. As is clear from these latter phrases, the underlying meaning of coup is ‘an instantaneous action’, not an act of force or violence. Looked at from this semantic point of view, therefore, the phrase coup de la glotte does not necessarily presuppose a forceful action, but rather a sudden, clean start at the glottis. Garcia, of course, raised and educated vocally as he was, could never have contemplated anything else. In the century and a half which separates us from Garcia’s treatise, there has been much confusion and muddle as various theories have flared up and vanished, but during much of this time one enduring warning light has shone out – that the coup de la glotte is dangerous. It has been equated with a violent, unprotected blast of air at the cords, commonly known as the hard attack. However, logic would imply that if the breath is always controlled at the cords, then a hard unprotected attack is impossible. This is certainly what Garcia believed and a close reading of his section on the ‘Articulation of the Glottis’ shows this to be so. Without a clean start, either piano or forte, no word beginning with a vowel can commence. All vowels must have a precise start, he states. He is scathing on the practice of beginning vocal exercises with a consonant – la, ma, na, pa, etc. and explains that such practices disguise faulty articulation of the glottis. He is equally painstaking and forthright on the physical separation of vowels and consonants in Italian – the one emanating from the throat and the other located wholly in the mouth. In retrospect, it is easy to see how Garcia’s phrase became misunderstood and misinterpreted as the world changed during his 101 years. A fatal mixture of new ideas and careless translation caused his phrase, straightforward to a Frenchman, to be disbelieved, rejected, and later in the twentieth century, even reviled. Many generations of singers have been taught to recoil from the infamous ‘hard attack’ in horror. Their teachers seem never to have gone to the source and checked on Garcia’s words and meaning; thus confusion on this subject has gone on for over a century. Teachers and singers in every generation have been aware of the eighteenth century concept of the clean attack of the sound as an essential element in good vocal technique; and yet most have accepted that the coup de la glotte is something to beware of. Few have gone to the trouble to find out that his use of the phrase was a genuine attempt to describe the result that everyone seeks: a precise and exact onset so that the voice speaks immediately, without tension, violence or fuss. The need for such a start is paramount. One should never forget Garcia’s other memorable phrase – ‘Once the vocal cords become vibratile, all control over them is lost’. 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Treaty of Zadar The Treaty of Zadar, also known as the Treaty of Zara, was a peace treaty signed in Zadar, Dalmatia on February 18, 1358 by which the Venetian Republic lost influence over its Dalmatian holdings. The Treaty of Zadar ended hostilities between Louis I of Hungary/Croatia and the Republic of Venice, who were contesting control of a series of territories along the eastern Adriatic coastline in present-day Croatia. Background In 1301, the Árpád dynasty was dissolved and, following a brief interlude, was replaced by the Angevin dynasty as the rulers of Hungary and Croatia. The first Angevin king was Charles Robert, who ruled from 1312 to 1342. He was supported by the most powerful Croatian nobleman Pavao Šubić, Prince of Bribir and Ban (viceroy) of Croatia, ruler of the coastal cities of Split, Trogir, and Šibenik. Pavao became the Ban of Croatia, conferring on him many of the powers of a monarch including minting coinage, conferring charters on cities and levying annual taxes on them. Pavao's actions led to a revolt among the Croatian nobility, who successfully reached out to King Charles to help them remove Pavao. In exchange for his aide, however, the Croatian nobility was forced to declare their direct allegiance to the Hungarian monarchy, setting the stage for Hungarian attempts to expel the Venetian Republic from the Croatian coastline. While the other cities in the Dalmatian region were suffering from tug of war between the Venetians and the Hungarians and Croatians, Dubrovnik, which was held by Venice, was growing into an economic power house by exploiting its position between the west and the mineral-rich kingdoms of Serbia and Bosnia, as well as Dubrovnik's broader location between Europe and the Levant. In the 1350s King Louis I was able to assemble a force of 50,000 men by joining his forces with reinforcements sent by the Duke of Austria, the Counts of Gorizia, the Lord of Padua, Francesco I da Carrara, and the Patriarchate of Aquileia, a state within the Holy Roman Empire. In 1356, the coalition besieged the Venetians at Asolo, Conegliano, Ceneda and the stronghold of Treviso. At the same time, along the Dalmatian coast, the army had attacked the Croatian cities of Zadar, Trogir, Split and Dubrovnik, as well as other smaller towns that surrendered fairly quickly. Broken by a series of military reversals suffered in the territory under their control, the Venetians resigned themselves to the unfavorable conditions stipulated in the Treaty of Zadar, which was signed in the eponymous city on February 18, 1358. Consequences The treaty was signed in the Closter of Monastery of St. Francis and based on the terms of the agreement, the Dubrovnik region and Zadar came under the rule of the King of Hungary and Croatia. It marked the rise of the Republic of Ragusa as an independent and successful state. The same cannot be said for Zadar since it was later sold back to Venice by Ladislaus of Naples. As a result of the peace treaty, Venice had to give all its possessions in Dalmatia to the King, from the Kvarner to the Bay of Kotor, but could keep the Istrian coast and the Treviso region. It was also forced to cancel, in the title of its doge, any reference to Dalmatia. However, the treaty preserved Venice's naval predominance in the Adriatic Sea as the King Louis accepted not to build a fleet of his own. Louis and his army triumphantly entered Zadar in 1358 by granting extensive privileges to the nobility of Zadar and erecting the city capital of Dalmatia. See also List of treaties References External links Zadarski list Kako je i zašto Ladislav prodao Dalmaciju, June 7, 2008 Zadar Category:14th century in Croatia Category:Wars involving medieval Croatia Category:History of Zadar Zadar Category:Treaties of the Republic of Venice Zadar Category:Treaties of the Kingdom of Hungary (1000–1918) Category:History of Dalmatia Category:1358 in Europe Category:14th century in the Republic of Venice Category:14th-century military history of Croatia	3.546875	4	[ -0.035400390625, -0.0020904541015625, -0.00885009765625, 0.00518798828125, 0.007781982421875, -0.00811767578125, -0.014892578125, 0.003997802734375, -0.01226806640625, 0.01434326171875, -0.0069580078125, 0.0035247802734375, -0.038330078125, -0.0203857421875, -0.0281982421875, -0.009521484375, -0.0062255859375, 0.00836181640625, 0.0235595703125, -0.024658203125, -0.05810546875, -0.0032501220703125, 0.021484375, 0.00537109375, -0.0152587890625, -0.0034637451171875, 0.0009765625, 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Kappa is a water demon whose mentions are found in ancient folklores of Japan. While some refute its existence by calling it a creature of imagination originating out of sightings of giant salamanders of Japan, others still hold the believe that Kappa is not confined to myths. In fact, some people actually consider that Kappa is very much real. Those who consider it to be real now have a support in their favor. Scientists have obtained very unusual mummified remains of a creature that are very much aligned with the characteristic features of the mythical demon. As a matter of fact, the discovered remains went for display in Kyuushuu island of Japan. How does a Kappa look like? The word Kappa literally translates into ‘river child’. The creature has been described to have a spiky and scaly body of a tortoise with a reptile-like blue or green skin. The limbs of the creature are described to be webbed and it is said to have a beak. If that isn’t just enough, what’s really unique to the creature is a hollow structure on top of its head. While the folklores say that Kappa is primarily a water creature, it also occasionally roams around on land. The hollow on its head is meant for holding water to keep it wet enough so that it does not loses its powers on land. What makes Kappa a demon? This lakes, rivers and ponds dwelling creature is said to be a demon. According to legends, the creature captures and devours children who are disobedient. What’s really interesting about this description is that Kappa turns out to be a selective demon. Kappas are often also depicted as mischief creators often attacking women and drowning animals and people. They are also said to make rude sounds as part of their mischievous behavior. About the mummified remains Scientists have gotten their hands on unusual mummified remains of a creature. The remains include an arm with attached hand and a foot. It is said that the remains were given to Miyakonijo Shimazu family in 1818 after one of the legendary creatures was shot dead. No other details are available. For instance, no one knows who shot the creature or why the rest of the body is not available. The remains went for display in Miyazaki prefecture at Miyakonijo Shimazu Residence. Scientific literature on Kappa During Japan’s Edo period, much of scientific work was devoted towards Kappa study. One such collection of Kappa information is Suikokouryaku of 1820. The information found in this compendium has information sourced from various Chinese and Japanese sources. Suikokouryaku contains several interesting drawings of Kappa. Killing a Kappa is not that difficult As per legends and folklore, Kappas are very much obsessed with manners. On land when someone bows, the Kappa will return the gesture by bowing. So in order to kill a Kappa, one should deep bow and as Kappa returns the gesture with a deep bow, the water in the hollow on its head falls off, rendering the Kappa powerless. It is then that a Kappa can be killed easily. Other mummies of Kappa Apart from the scattered remains obtained from the Miyakonijo Shimazu family, there are a number of other mummies on display which are claimed to be Kappa mummies. Some of these mummies are pictured above. Arguments by skeptics Skeptics say that all the mummies that are on display and are claimed to be Kappa mummies are not real. They say that these mummies are works of artists from Edo period that lasted from 1603 to 1867 and that they were created using different animal parts like monkeys, stingrays and owls. So, what do you think? Are Kappas real? Drop your comments below and let us know. 1 comment Theo Davis MannMarch 18, 2017 - 12:48 am I believe that the current American “fake news” fad/controversy is not NEARLY as interesting as this! At least here, you have some substance, quite literally, that can be objectively analyzed by science (although it doesn’t seem to be happening…where’s the DNA testing)- vs contentious 2-party politics that are just…… so pathetic and nonsensical.	3.25	3	[ 0.01409912109375, 0.0130615234375, 0.0079345703125, 0.0177001953125, -0.005401611328125, -0.00439453125, -0.00750732421875, 0.0001468658447265625, -0.0157470703125, 0.01397705078125, 0.01251220703125, -0.004730224609375, -0.01397705078125, 0.003509521484375, -0.00439453125, 0.0035552978515625, -0.0147705078125, 0.0035858154296875, 0.0120849609375, 0.00665283203125, 0.03466796875, -0.00958251953125, -0.016357421875, 0.007598876953125, -0.0279541015625, -0.005126953125, -0.002227783203125, -0.011474609375, 0.0238037109375, -0.01025390625, -0.01361083984375, 0.00146484375, -0.03271484375, -0.0026397705078125, 0.00445556640625, 0.01251220703125, 0.01031494140625, 0.01495361328125, -0.0234375, 0.00445556640625, -0.0023651123046875, 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MyAccess Sign In About MyAccess If your institution subscribes to this resource, and you don't have a MyAccess Profile, please contact your library's reference desk for information on how to gain access to this resource from off-campus. Introduction The knee, which is a gliding hinge joint, is the largest synovial joint in the body. Its small area of contact of the bone ends at any one time makes it dependent on ligaments for its stability. Although this allows a much increased range of movement it does increase the susceptibility to injury, particularly from sporting activities. Finding the cause of a knee problem is one of the really difficult and challenging features of practice. It is useful to remember that peripheral pain receptors respond to a variety of stimuli. These include inflammation due either to inflammatory disorders or chemical irritation such as crystal synovitis, traction pain (e.g. trapped meniscus stretching the capsule), tension on the synovium capsule (e.g. effusion or haemarthrosis), and impact loading of the subchondral bone. Disorders of the knee account for about one presentation per 50 patients per year.1 The commoner presenting symptoms in order of frequency are pain, stiffness, swelling, clicking and locking.1 The age of presentation of a painful knee has varied significance as many conditions are age-related. Excessive strains across the knee, such as a valgus-producing force, are more likely to cause ligament injuries, while twisting injuries tend to cause meniscal tears. A ruptured anterior cruciate ligament (ACL) is a commonly missed injury of the knee.2 It should be suspected with a history of either a valgus strain or a sudden pivoting of the knee, often associated with a cracking or popping sensation. It is often associated with the rapid onset of haemarthrosis or inability to walk or weight-bear. A rapid onset of painful knee swelling (minutes to 1–4 hours) after injury indicates blood in the joint—haemarthrosis. Swelling over 1–2 days after injury indicates synovial fluid—traumatic synovitis. Any collateral ligament repair should be undertaken early but, if associated with ACL injuries, early surgery may result in knee stiffness. Thus, surgery is often delayed. With isolated ACL ruptures, early reconstruction is appropriate in the high-performance athlete; otherwise, delayed reconstruction is appropriate if there is clinical instability.3 Acute spontaneous inflammation of the knee may be part of a systemic condition such as rheumatoid arthritis, rheumatic fever, gout, pseudogout (chondrocalcinosis), a spondyloarthropathy (psoriasis, ankylosing spondylitis, reactive arthritis, bowel inflammation), Lyme disease and sarcoidosis.	3.0625	3	[ 0.0025177001953125, -0.005035400390625, 0.0245361328125, -0.01470947265625, -0.0145263671875, 0.00183868408203125, -0.007293701171875, 0.0125732421875, 0.0023956298828125, -0.03515625, -0.01324462890625, -0.01446533203125, -0.0162353515625, -0.00081634521484375, -0.00194549560546875, 0.003387451171875, -0.004608154296875, 0.01806640625, -0.0004100799560546875, 0.002044677734375, 0.00909423828125, 0.00201416015625, 0.0079345703125, -0.0225830078125, 0.000461578369140625, 0.00799560546875, 0.00946044921875, 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X-rays and visible light from the radio galaxy 3C31, located 240 million light-years from Earth. Calculating how fast such galaxies spin doesn’t need to take dark matter into account, according to a new paper. X-ray: NASA / CXC / Univ. of Bristol / M. Hardcastle et al; Optical: NASA / STScI Some 80 years after dark matter was first theorised, we still have no idea what it is. Now, a new study casts doubt on its existence altogether. According to the standard model of cosmology, the immense gravity of dark matter is crucial for explaining why galaxies can spin so fast without tearing themselves apart. But in work just accepted by Physical Review Letters, a team of American astronomers found a striking correlation between the visible matter (the stars and dust in galaxies) and its rotation speed. That means they can predict the rotation of galaxies – without invoking the dark stuff at all. {%recommended 889%} “Nothing in the standard cosmological model predicts this and it is almost impossible to imagine how that model could be modified to explain it, without discarding the dark matter hypothesis completely,” said David Merritt, an astrophysicist at Rochester Institute of Technology in New York and who was not involved in the research. Gravity at the level of the solar system is a piece of cake. Simple laws, written by Johannes Kepler in the 1600s, tell us that a planet’s orbital speed depends precisely on its distance from the sun. So while Mercury whizzes around the sun at an average of 47 kilometres per second, Pluto shuffles along at just a 10th that speed. The weird thing is, galaxies don’t behave this way at all – stars don’t slow the further they are from the galactic centre. In some cases, they speed up. According to our current understanding of gravity, stars at the edges of galaxies, such as our sun, should be flung out into deep space. In the 1970s the American astronomer Vera Rubin, picking up an idea pitched by Swiss astronomer Franz Zwicky a few decades before, suggested an answer: there must be extra matter in and around the galaxies – perhaps 10 times more than what we can see – holding everything together. But after 40 years of fruitless searching, some physicists think the hunt for dark matter has been a wild goose chase. {%recommended 1150%} In the new work, a team led by Stacy McGaugh at Case Western Reserve University in Ohio found a direct relationship between the distribution of regular matter in a galaxy and its speed of rotation. This distribution held, even for galaxies thought to be dominated by dark matter. McGaugh’s team pored over data from 153 galaxies collected by NASA’s Spitzer Space Telescope. Imaging in the infrared, Spitzer can see both the stars and the immense clouds of dust between them – and these components allowed McGaugh’s team to calculate the mass of the visible matter in each galaxy more accurately than ever before. Then they compared these masses against the actual rotation speeds of each galaxy, which were clocked by astronomers for decades. Surprisingly, for dark matter advocates at least, the measurements showed a tight correlation. This means the team could look at a galaxy’s visible matter and predict its rate of spin. The relationship is strong enough to be termed a new law of nature, “a sort of Kepler’s law for rotating galaxies,” the authors write. The result was consistent over 2,693 data points across 153 galaxies with a huge variation in body shape – from dwarfs to giants, from spiral-armed or irregular beasts, some with central bulges and others without – all without accounting for dark matter. {%recommended 1936%} The question is, why? Perhaps our understanding of gravity is fundamentally wrong. One theory waiting in the wings is modified Newtonian dynamics which says that gravity behaves differently at very large distances. It has been successfully applied to galaxy rotation too. But it is far too early to throw dark matter out. For starters, there is plenty of evidence beyond galactic rotation that tells us dark matter must be out there. While McGaugh admits the findings could stem from modified gravity, it could also be telling us something about the nature of dark matter itself. For instance, the spread of dark matter and regular matter could be more intimately linked than previously thought. Besides, the new work shows correlation, rather than causation, but one that, in the words of the author, “demands explanation”. “Most importantly, whatever theory you want to build has to reproduce this,” says McGaugh.	4.1875	4	[ 0.01019287109375, -0.01214599609375, 0.00057220458984375, 0.01141357421875, 0.000614166259765625, 0.0018157958984375, -0.014404296875, 0.00543212890625, -0.00823974609375, -0.006072998046875, -0.002288818359375, 0.006988525390625, 0.00035858154296875, 0.0087890625, 0.006195068359375, -0.0130615234375, -0.0010833740234375, 0.0014495849609375, 0.01025390625, 0.01104736328125, 0.053466796875, -0.00543212890625, -0.010986328125, 0.004791259765625, 0.00494384765625, -0.0021209716796875, 0.0013427734375, -0.012451171875, 0.0036163330078125, 0.00799560546875, 0.0084228515625, -0.00099945068359375, -0.007720947265625, -0.00732421875, -0.004364013671875, 0.00799560546875, 0.01202392578125, 0.006500244140625, -0.0047607421875, -0.00750732421875, -0.0072021484375, 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A man's chances of survival depended on how quickly his wound was treated. Modern warfare was now producing vast numbers of casualties requiring immediate treatment at the same time. This necessitated an efficient system that could immediately address a patient’s critical injuries close to the Front and then evacuate him to a medical unit in a safer zone. This network is known as the Medical Chain of evacuation or evacuation chain. The secret of success in treating large numbers of casualties was rapid evacuation. “All through the chain of Medical Units from the Front to the Base the wounded man is kept the very minimum of time to attend to his wounds, and then he is moved on, and kept on moving, until he reaches either the Base or Home..... The reason for rapid evacuation is twofold. Firstly, it is very bad for morale if troops see wounded men lying about in large numbers; and, secondly, unless Medical Units are cleared they lose their mobility, and also cannot deal with a fresh influx of wounded that might come in quite unexpectedly - e.g. from a surprise counter-attack.” [Lt/Col T B Nicholls R.A.M.C. ‘Organization, Strategy and Tactics of The Army Medical Services in War’] The rapid and successful evacuation of any casualties, whether on a battlefield or in civilian life, depends on three interdependent factors - time, space and transport. Time involves how quickly wounds receive first aid so infection does not set into the wound, and/or the casualty does not bleed to death. It also involves how quickly the casualty can get to someone with specialized knowledge or with specialist equipment. Abdominal wounds, for example, need to be operated on within six hours in order for the patient to survive. Transport involves what type of equipment can be used and/or is readily available to transport the casualty away from danger and to an appropriate medical facility. This process could involve the soldier walking or being transported on stretchers, horses, cars, trains, barges or ships. Space involves what is happening in the immediate area such as: how close can emergency services get without becoming casualties themselves? What is topography and how does it help or hinder? Is there enough space to set up a large medical facility close by or is there only enough room for a small one? With the above in mind, other factors had to be considered: • Mobility: All medical field units needed to be able to move at a moments notice. This was essential to ensure the fighting units had medical support during an advance or retreat. The procedure for a significant advance was for each medical unit to move forward to one already up and running in front of them. Therefore, the Regimental Aid Post would move forward in line with the fighting soldiers. An Advanced Dressing Station would then move forward to a Regimental Aid Post. The Main Dressing Station would move forward to an Advanced Dressing Station. A Casualty Clearing Station would move forward to a Main Dressing Station, and a Stationary Hospital would move to fill the gap between the Casualty Clearing Stations and the General Hospitals near the ports. In a retreat the procedure would be same but in the opposite direction. This was achieved by a small ‘light section’ of each unit moving forward immediately. They would provide care for the serious cases still housed in the unit ahead who were unable to be moved. The rest of the unit would then evacuate less serious cases, then would close, pack up and move. • Distances between medical units: Sometimes the nature or physical features of the area (due to unsuitable topography for motor transport, bad weather, or deteriorated land due to heavy shelling) prevented medical units from getting optimally close. In these situations Relay and/or Collecting Posts were set up where patients could be collected and transported by horse drawn ambulances. (These will be explained further in the Field Ambulance and Casualty Clearing Station sections) • Overlapping areas: During a major offensive, the front Line might cover some 5 to 6 miles with many Corps/Brigades/Regiments involved, all of which would have had their own pre-allocated medical support. In situations where the areas of advance were narrow, it was inevitable that their medical support would overlap. In these cases medical units from different Divisions would either work together as one, or perhaps two or three different medical units would set up in one specific location. • Co-Operation: It was imperative that the medical evacuation chain did not hinder the fighting troops going into action or prevent them from getting to their ammunition, and vise-versa. Also the Medical Services was reliant on other branches of the army to supply materials to build Dressing Stations, construct roads, railway sidings, and/or provide telephonic communications. • Before the start of any major offensive the Directors and Assistant Directors of Medical Services (DMS and ADMS) who were appointed to oversee in the offensive held a conference to discuss all the above factors before setting up the evacuation chain for that sector. Collecting Zone: Regimental Aid Posts and Field Ambulances Regimental Aid Post. [RAP] and the role of the Regimental Medical Officer [RMO] “I should not advise anyone with any desire to practice their surgical or medical skill to take on the job of medical officer to a battalion, but from the point of view of seeing the war, understanding military methods and the spirit of the men it is the best post open to a medical man..... The only diseases the M.O. is called upon to treat are slight sprains, myalgia, and last, but not least, diarrhea.... Sanitation is, perhaps, the most important work that the M.O. is called upon to perform.” [Lt A Noel Garrod R.A.M.C. ‘Notes on the Existence of a Regimental M.O. - At the Front’] Duties of the RMO: During the war every fighting unit (infantry battalion, artillery brigade or cavalry regiment) had it’s own doctor [or RMO]. He was RAMC but came under the commanding officer of the fighting unit he was attached to. The doctor’s role was not only to attend to medical matters but also matters of hygiene, which meant water supply, the preparation of food, and the supervision of sanitary areas all came under his control. The doctor’s daily routine usually began with him doing an inspection of the sick. He then inspected the camp or billets, and the cook houses. The rest of the day would be taken up with the training and supervision of water cart orderlies and stretcher-bearers. To assist him in his duties he would have had an RAMC Sergeant or Corporal attached to him and perhaps 1 or 2 RAMC Privates. When away from the Front Line, the doctor’s post was known as the Camp Reception Station [CRS] or Medical Inspection Room [MI Room] and contained 2 - 6 beds for short term holding for those needing rest but was not sick enough to be evacuated back. “A good M.O. to a battalion was a privileged and important officer. He was usually on intimate terms with his colonel, a friend to all his brother officers, and friend and confidant as well as doctor to the rank and file. Often and often I noticed that a battalion with a first-class M.O. was always a first-class battalion, had the smallest sick parade, fewer men falling out on a long march and the lowest quota of casualties from trench foot.” [Capt Philip Gosse R.A.M.C. ‘Memoirs of a Camp-Follower’ Function of the RAP: When in the trenches the doctor’s post was the RAP. The objective of the exercise was to patch up the wounded and either return them to their duties in the line or pass them back to a Field Ambulance. The RMO had the same staff as mentioned above but this became augmented by a designated number of Stretcher-Bearers. These Regimental Stretcher Bearers came from the fighting unit the RMO was attached to, usually the regimental bandsmen. When under pressure, the RMO could be further assisted with bearer teams from a Field Ambulance. Every soldier had a special pocket in his uniform for his issued ‘First Field Dressing.’ It contained antiseptic pads and two bandages (one for entry wound, one for exit) in a waterproof cover. This dressing was applied by a regimental stretcher-bearer, a comrade, or by the wounded soldier himself, if he was able, in the firing line. If the wounded man was unable to walk, he was carried back via hand or wheeled stretcher to the RAP. The regiment stretcher-bearers had then fulfilled their duty, and it became the RMO’s responsibility for receiving the wounded man, and treating him by checking the dressing, overseeing the splinting of fractures, and ensure everything was being done to stop the patient going into shock. If morphine was given or a tourniquet applied, the soldier’s forehead was marked with a “M” or “T”. If required he would undertake an emergency amputation but large operative treatments were discouraged so close to the fighting and danger. The RMO also completed a Field Medical Card for each patient and fixed it firmly to the patient—generally attaching it to a button by its attached string. This card included the soldier’s name, rank, and unit, a diagnosis, and any special treatments (like operations) performed. As the patient moved down the evacuation chain, the Field Medical Card remained with him so that information could be added to it and his full treatment could be known. The patient was then taken to a designated collecting area to be picked up by stretcher-bearers of the Field Ambulance. Equipment: According to Dr John S G Blair “The basic MO’s drug box in 1914 included phenacetin for headaches, Adrenaline in injectable form, 0.0003gm, one dose to be used as a stimulant.... Dover’s powders for colds, Bismuth salicylate for the stomach, cough medicine, a light aperient calomel, and a strong one, unspecified; quinine sulphate, 2gr (60mg) as a tonic, lead and opium tablets to be made into a lotion as an application for sprains or as an anti-diarrhoeal and, for the doctor to hold safely, morphine sulphate gr 1/4 or grl 1/2 (15 or 30mg). Morphine was to be given “under the tongue or by injection.” There were also methylated spirits, iodine, boric lotion and carbolic acid 1 part in 60 as antiseptics for wounds, Lastly there was sal volatile, to be given for ‘fainting, a few drops in water’.” [Dr John S G Blair ‘Centenary History of The Royal Army Medical Corps]. Equipment at the RAP was supplied by the Field Ambulances and normally consisted of a primus stove and a beatrice stove, along with an acetylene lamp, anti-tetanus serum, assorted bandages, blankets, Boric ointment, cotton wool, first field dressings, plain gauze, shell dressings, Sulphur ointment and a vermoral sprayer. There was also reserve boxes of all of the above, and a hamper containing medical comforts such as brandy, cocoa, bovril, oxo, biscuits etc. Site (time and space): Location requirements: The site of the RAP came under the concern of the officer commanding the fighting unit. It was ideally situated a few metres behind the front line, but near the regiment’s headquarters so the RMO could be provided with early information about the tactical situation. It was also to be located central so it could be easily accessed from any part of the front line in which the regiment is engaged by the wounded. Also in a place that was sheltered to protect all from enemy fire, and easily accessible to the field ambulances who were next in the line of evacuation. Typical facility: RAP’s were usually situated in a dugout, in a communication trench, a ruined house, or a deep shell hole. In areas where constant fighting had occurred over a long period of time, such as Ypres, there was very little cover left so a RAP might have been set up behind a burnt out tank. RAP’s had no holding capacity for the wounded. If the engagement was successful then the RMO moved forward and searched out another area which would come into the above criteria. A yellow flag was put up so that the wounded could find it and runners might be expected to run back to advise the ADMS and the Field Ambulances of the new location. Transport: The RMO was equipped with a horse for his personal use, and a Maltese Cart (a two-wheeled cart suitable for conveying a lying patient) and driver. Alternatively these might have been a light motor van and a small motor-car or a motor-cycle combination. As noted above the RAP would have stretchers for hand carriage and/or wheeled stretchers. The Field Ambulance (of infantry divisions) General definition The Field Ambulance was a complete medical unit made up of previously separate and independent entities. These were The Bearer Division [previously working as Bearer Companies]; The Tent Division [previously working as Field Hospitals] and The Transport Division [Army Service Corps (to be explained further in the Transport of Sick and Wounded section)]. Personnel The Field Ambulance at full strength composed of 10 Officers and 224 men. The Bearer Division had 18 stretcher squads each of 6 men. The Tent Division was comprised of doctors: 9 medical officers and 1 dental officer, as well as 1 Quartermaster of stores, batmen, clerks, cooks, dispensers, nursing orderlies, and the Transport Division, which had 60 men attached from the Army Service Corps. All this made up medical support for one infantry brigade. [Three to every Division]. Each brigade was made up of three to four battalions, so in order to perform it’s duties satisfactorily, the field ambulance was divided into A, B and C Sections These three sections were all capable of carrying out independent action. The headquarters of the Field Ambulance always formed part of ‘A’ Section. The three sections were further sub-divided into three parts to incorporate the bearer division, the tent division and the transport division. Function of the Field Ambulance When away from the trenches a field ambulance’s role was to keep the fighting men fit and healthy. This was achieved by setting up Divisional Rest Stations [DRS] and baths (usually sited in a Brewery where up to 50 men could be bathed at a time in the large vats). They were also allocated special tasks such as providing treatment at scabies centers or other ailments. When in the trenches its role was similar to modern day emergency ambulance services: to collect and transport patients to someone with specialized knowledge or to specialist equipment, whilst monitoring them, and treating them if necessary to ensure their condition remains stable. The personnel serving in the field ambulance achieved this by setting up various designated posts and sections according to distance from the RAPs to the Casualty Clearing Stations. The Bearer Division were the stretcher-bearers responsible for collecting the wounded, whilst the Tent Division were the medical staff responsible for the treatment of their wounds. Before any major offensive, the three Field Ambulances of a Division joined together and acted as one to form and oversee the various posts and stations. One way of knowing how the field ambulances were arranged for any particular battle is to look at the war diary of the ADMS of that Division. The various designated posts and sections of a Field Ambulance: Advanced Dressing Stations [ADS]: Location and Construction: There were normally two ADSs to every Division. In areas where the Divisional line became narrow one ADS would be established for the sole use of that Division and one would be shared with the Division to their left or their right. ADSs were set up as far forward as military conditions would permit. Ideally, this was about 400 yards behind the RAPs. Preferable locations were large houses, schools or churches but tents were used where necessary. In all events they needed to provide living accommodation for the officers and men; shelter from the weather; be inconspicuous and provide protection from the enemy, and had to be easily accessible with an entrance and an exit. Personnel: The personnel of each ADS were 3 officers and 53 ordinary ranks. Of these 1 officer was the Officer Commanding. 36 Privates would be employed as stretcher-bearers, with 1 officer supervising them. The others would be employed as clerks, dressers and cooks. If the ADS became overwhelmed with casualties the above personnel could increase. Equipment: Typical equipment for the ADS included stretchers, notice boards and flags for marking routes, empty petrol tins for water and kettles, hot water bottles, acetylene lamps, blankets, ground sheets, pyjama suits, stomach warmers, anti-tetanus serum, chloroform and No 1 Field Pannier, which included: wool, gauze, plain lint, shell dressings, 3 and 6 inch and triangular bandages, a jaconet and a calico, towels, nail brushes, safety pins, plasters, towels, tourniquets, a tincture of iodine, rum jars filled with eusol, and splints for leg and back as well as the Thomas splint. Duties: The ADS was the first line of documentation for the RAMC, [i.e. Admission and Discharge books, war diaries etc]. Stretcher-bearers went forward and collected the sick and wounded from the RAP and carried them back to the ADS. A patient’s medical condition was then assessed to make sure bandages had not loosened or become too tight, and also that the patient was not haemorrhaging or going into shock. Special attention was given to those marked with a “M” or “T” (morphine or tourniquet) at the RAP, and careful examination was given to see if the tourniquet needed to remain or not. Surgery was not undertaken at an ADS unless absolutely necessary as it had no holding capacity. It was simply an intermediate stop to assess the patient. Those who were deemed to be urgent cases were transferred to the Main Dressing Station. Those who were not deemed as urgent cases were transferred straight to the Casualty Clearing Stations. “It was now eleven o’clock of a pitch black night with threatening rain... We were in for a busy night, for all the stretcher parties from the various ambulances were out in the field collecting the wounded, whose arrival was expected now at any moment. An operating tent had been pitched in the field near by, and was brilliantly lit up with a huge acetylene lamp. The operating table was fixed in the centre of the tent and along each side were the instruments, basins, and dressings lying on the lids of the panniers, which made excellent side-tables. Very soon the ambulances lumbered up with the men picked up from the fields close at hand. The stretchers, each holding a wounded man, were taken out of the waggons and laid on a heap of straw near the door of the operating tent. Sixteen men were taken out and laid side by side. New Stretchers were put in the waggons, which again set out to bring in more wounded. One surgeon stood on one side of the operating table, another stood opposite him, and a third surgeon was ready to assist or give an anaesthetic if necessary. Quietly and quickly one wounded man after another was lifted on to the table, his wounds were speedily dressed, and he was again carried out and laid on the straw with a blanket below and another above him. Those with painful wounds were given hypodermics of morphia. All who were fit to take nourishment had hot soup, tea, bread and jam. Stimulants were given freely to those requiring it. The wounds were mostly from shrapnel, and only one case required an anaesthetic. He had a bad compound fracture of the thigh and was in terrible pain. We made some good splints and fixed up the limb comfortably and in good position. One poor devil had a bad abdominal wound for which we could do nothing. He was given a good dose of morphia and slept quietly till five a.m., when he ceased to breathe. At one o’clock in the morning wounded were still coming in, and the surgeon on duty was relieved by myself. So with coat off, bare arms and covered with an operating apron, I did my spell of surgical duty during that night on the banks of the Marne. Our stretcher parties at last were finished, and had all come in with the report that all wounded had been brought in...... At six o’clock our large list of wounded were sent off the railhead at Coulommiers on returning-empty supply waggons and under the charge of a medical officer. The operating tent was struck and all the panniers and equipment were packed. The Field Ambulance had done its ‘job’.” [Lt Arthur Anderson Martin R.A.M.C. ‘A Surgeon in Khaki’] Main Dressing Stations [MDS]: Location and Construction: There was normally one MDS to every Division. They were formed by the Headquarters of the Field Ambulance [section A]. Ideally MDSs were sited roughly one-mile behind the ADSs. But in the Great War this was seldom the case, partly due to topography, but also because a MDS needed approximately 300 X 200 yards of space to provide sufficient room should it be taken over by a Casualty Clearing Station during an advance. The ideal location was a large building where water, light, heating and drainage were already supplied. If no buildings were available, then roughly 9 tents were used, with 1 reserved as an operating room. MDSs needed to be located between the ADS and the Casualty Clearing Stations, closer to the latter if possible. They did not need protection from shell fire, but cover from the splinters of bombs had to be taken into account. Structure: Every MDS was organised with six sections: 1) Receiving Section provided hot drinks, sandwiches, and cigarettes. 2) Recording Section where clerks took patient information and examined Field Medical cards 3) Resuscitation Section for warming and reviving those suffering from shock or the effects of haemorrhage. 4) Dressing Station where dressing were applied, and any urgent surgical treatment, administration of A.T.S. or morphia, if not carried out already. 5) Gas Section to keep gas victims away from other patients. 6) Evacuation Section where the patient’s treatment was classified with whatever they were suffering from and how they were treated, and they awaited evacuation. Other space was allocated for a mortuary, a cookhouse, stores, and living accommodation for officers and others ranks. Personnel: The personnel of each MDS included the Officer Commanding, 2 Medical Officers, a Dental Officer, a Quartermaster and 59 other RAMC ranks, along with 1 Royal Army Service Corps officer, and 44 other ranks ASC attached. Equipment: Typical equipment at the MDS was very much the same as the ADS, with additions of oxygen apparatus, operating lamps collapsible trestles and a field dental outfit. Duties: The MDS was further away from the firing line so was able to be better equipped to provide accommodation and treatment than an ADS. Urgent operations were more readily performed, and better arrangements could be provided for the resuscitation of those suffering from shock or haemorrhage, or both. Walking Wounded Collecting Posts [WWCP] During a major offensive the ADS quickly became congested. If it were pre-judged that this was likely to happen, then a WWCP was set up - one to every Division. It was generally believed that the walking wounded were able to walk slightly farther than the ADS, therefore a WWCP was often constructed at a location between the ADS and the MDS. Location: Ideally, a WWCP was sited with easy access from the front line and the ADS, and also close to a road leading to a Casualty Clearing Station so that transport could reach it. The route was set up close to the stretcher-bearers’ route in case the walking wounded man collapsed on his way to the WWCP. The route from the Front to the WWCP was clearly marked with notice boards or directing flags. The Post would have been sited behind the usual range of artillery fire but protection from splinters was accounted for it when a location was being formed - usually in a building or farm house but marquees were also used. Personnel & Equipment: The WWCP was staffed by personnel from a Field Ambulance section, but there were no specific arrangements, and there was no scale laid down for equipment. A suggested guide for equipment was 5 Thomas Splints, stretchers, blankets, waterproof sheets, soyer’s stoves, camp kettles, petrol tins for water, drinking mugs, and one medical companion and first medical panniers (pairs). Also dressings and light refreshments for approximately 300 cases. Structure: Similar to the MDS, the WWCP consisted of a Reception Section, a Recording Section, a Dressing Section, and an Evacuation Section. No operations or complicated dressing were done at the Posts. When leaving the Post, the wounded men were transferred to the MDS or the Casualty Clearing Station, whichever was deemed appropriate. Bearer Relay Posts [BRP] At times when it was impossible to get the ADSs optimally close to the fighting units due to unsuitable topography for motor transport, bad weather, or deteriorated land due to heavy shelling, the field ambulance set up relay posts. It was acknowledged at the time that bearers could not carry loaded stretchers more than half a mile over difficult ground, meaning that a relay post would be set up roughly every half a mile. There were no medical facilities set up at relay posts, they merely existed so that stretcher-bearers could pass their carry to the next set of stretcher-bearers and then return to the RAP to pick up new casualties needing to be carried. Collecting Posts [BCP, CCP or DCP] Collecting posts were set up where two or more evacuation routes met on the main route back from the Front lines. These could be Bearer Collecting Posts, where two or more relay posts merged, or could be set up further away from the front lines when evacuation routes from different Divisions or different Corps came together. Collecting Posts were mainly a holding area for wounded whilst they waited to be collected by either motor or horse transport. Although there were no medical facilities set up at these posts, they were often staffed by personnel from a Field Ambulance section to check dressings and supply a drink or something to eat. Transport Casualties were transport from the ADSs to the MDSs and Casualty Clearing Stations via horse wagons and motor ambulances. (to be explained further in the Transport of Sick and Wounded section) The Cavalry Field Ambulance (of cavalry divisions) General Definition: The definition and function of the Cavalry Field Ambulance was the same as the Infantry Field Ambulance. The difference is that is was smaller and because cavalry regiments were much more mobile than infantry regiments, their Field Ambulances had to be much more mobile. They would open, treat the wounded, then close and move much more frequently. “In view of the high degree of mobility requisite and the frequent moves that may be necessary, the personnel must be highly trained. Each man must know his job, and must be able to do it speedily. Loading, unloading, pitching and striking the shelter, together with arranging the equipment, must be practiced until this can be done in the minimum of time. An efficient team can establish the ADS in 10 mins” [Lt.Col E C Sandilands, RAMC ‘Journal of the RAMC, September 1935.] Personnel: Their personnel consisted of 6 Officers and 70 other ranks, RAMC. There were four Field Ambulances per Cavalry Division, each sub-divided into two sections; ‘A’ Section and ‘B’ Section. Procedure: “The usual procedure in action is that the ambulance is divided into tent and bearer sections, the former of which establish a temporary hospital of fifty beds some five miles behind the firing line. The bearer section goes forward and gets into touch with the regiment attached R.A.M.C. Officer at this regimental aid post when the cavalry are engaged in reconnaissance. From the aid post they will move cases in light wagons to the temporary hospital...... Professional work for officers consists of emergency operations and quick evacuation of wounded to the lines of communication. It does not burden itself with chronic cases, as it is a highly mobile force and must be ready to move forward at the shortest possible notice in conjunction with the cavalry brigade.” [Maj H Norman Barnett R.A.M.C. ‘The Work of a Cavalry Field Ambulance’] Evacuation Zone - Casualty Clearing Station. [CCS]. Main function: Casualty Clearing Stations were the pivot point in which the whole system of evacuation turned from collecting casualties to distributing them. When created in 1907, they were intended to act as sorting centres to facilitate the movement of casualties from the Field Ambulances onto the Base Hospitals. Their role was to act as a temporary reception area for the sick and wounded, and their prime duty was to arrange for and prepare patients for satisfactory evacuation rather than of active treatment. Their function, therefore, was similar to those of the Tent Division of a Field Ambulance but dealing with larger numbers of casualties and out of range of shell fire. As they evolved, however, their role became similar to modern day Accident and Emergency (A&E) Departments. Casualties were received, assessed, then divided into three categories (known today as triage). These categories were: Non-serious cases - to be returned to duty after recuperation and rest. Serious cases but still fit to travel - to be immediately evacuated back to the base hospitals. Serious cases in urgent need of immediate treatment. Casualties were provided with food and rest, and were prepared for their further journey, which could have been immediate or after recuperation. The main objective was to provide necessary treatment and move patients out as quickly as possible. However, as a result of their evolution and expansion, it became possible for recuperating patients to be retained for up to four weeks before being returned to their units or transferred to a General Hospital via Ambulance Trains or Inland Water Transport (barge). Evolution of their function: The discussion of CCSs is difficult to generalize because they were the one link in the evacuation chain that radically evolved over the course of the war. The CCS of 1914 was not the CCS of 1918. 1914 and 1915: CCSs mobilized in August 1914 under the title ‘Clearing Hospitals’. During the 1914 retreat, the equipment of most of the Clearing Hospitals was still in transit, consequently, they did not start to become fully effective units until early 1915. By this time it had become obvious to the medical services that there was public and professional confusion about the CCS’s role. Was it a sorting centre or a hospital as it’s title suggested? This resulted in their official title being changed to ‘Casualty Clearing Station’. In spite of the name change, very high volumes of urgent cases, (i.e, gas gangrene or abdominal injuries) arrived at the CCSs at an alarming rate. Unequipped to deal with this influx, in early 1915, the Director General of Medical Services (D.G.M.S.) approved the increase of surgical work and appropriated extra surgical equipment to be moved forward from the hospitals to the CCSs. By the middle of 1915 it became standard practice for head injuries, compound fractures, and penetrating wounds of the limb to be sent straight to CCSs. 1916: Despite surgery now taking place in CCSs, surgeons began arguing that facilities were required to enable surgery to take place even closer to the Front lines, to prevent a potentially fatal delay in the treatment of infected wounds. Post mortums of abdominal cases had revealed that most had died of hemorrhaging, which might have been avoided by earlier surgery. It was argued that Field Ambulances were not able to provide such facilities because of post-operative care - it was not advisable to move patients immediately after an operation and Field Ambulances were frequently on the move. Also, they were not in a position to provide patients with comfortable beds or nursing care, thus hindering a patients’ recuperation time, Arrangements for sterilizing instruments and gowns etc were also more difficult at Field Ambulances. All evidence indicated that the success rate for abdominal surgery was much higher when performed at CCSs rather than Field Ambulances, so all in all it was decided to bring CCSs in as close as 10,000 yards from the Front lines as opposed to roughly 20 kilometers away. This, however, resulted in them now coming under enemy attack, especially from aircraft bombing. Their positioning at railheads meant that CCSs were now becoming static and, despite the name change, were becoming more like hospitals. In some areas though, it was impossible to bring a CCS very close due to unfavourable topography. This resulted in the formation of Advanced Operating Centres and Abdominal Hospitals. (see ‘Formation’ section) 1917: By 1917, more operations were performed at CCSs than base hospitals. From 24th July 1917, the distribution of sick and wounded to CCSs was regulated in accordance of the D.M.S. of the Fifth Army to treat certain types of wounds. The Field Ambulances became the sorting centres, separating, for example head wounds from stomach wounds at the ADSs, and transporting them to the relevant CCS. Specific CCSs were also allocated to treat self-inflicted wounds, as well as infectious cases, and those who were gassed. Other measures established at CCSs in 1917 were surgical cleaning of wounds before evacuation to the base, the principle of retaining so-called shell shock cases, and measures to deal with mustard gas, which was used by the enemy for the time in 1917. Also by 1917 nursing sisters were successfully trained in the administration of anaesthetics, which was successful and freed up more than a hundred medical officers for other duties. 1918: The spring 1918 German offensive placed the CCSs in danger of becoming part of front line action, which caused them to become mobile again and retreat. By June 1918 they had reduced in size, and many had lost their equipment to the enemy - some sent by transport to a different location, and some taken by the enemy. They were no longer situated on railheads or in other areas designed to promote easy evacuation of the wounded because they had been on the move. By the time of the Allied Counter-Offensive in August, they had recovered their losses, but it was agreed, that although they would be placed as far forward as possible, they must remain sufficiently mobile to keep up pace with any advance or retreat. Personnel: In normal circumstances CCS personnel would included 8 Medical Officers (The C/O, 6 doctors, and 1 surgical specialist), 1 Quartermaster, 7 QAIMNS, and 77 other ranks (working as clerks, cooks, nursing orderlies, theatre orderlies, stretcher-bearers etc.) Often a dentist and a pathologist were attached. Non-medical personnel attached would include 3 chaplains, 4 lorry drivers, 2 Royal Engineers personnel - an electrician and engine hand, and men from the Army Service Corps, employed as ambulance drivers. This small staff was sufficient in quiet times but totally inadequate during battle. In times of heavy fighting, the number of personnel could be increased and specialized by bringing ‘Surgical Teams’ forward. A surgical team was made up of a surgeon, an anaesthetist, a theatre sister, 2 theatre orderlies, 4 stretcher bearers, and a batman. The extra personnel were brought in from hospitals at the base, or from CCSs and/or Field Ambulances which were not engaged in active operations. Additional nursing sisters were also attached in proportion from 7 to 24 or more. The organization for reinforcements during a major battle gave no provision for additional rank and file, (i.e. men to assist with the unloading of motor ambulance cars as they came in, and loading patients onto ambulance trains.) To meet this demand, detachments of 50 or more low category men, or men from labour companies or other sources, or even convalescent patients were attached to CCSs. Formation/Location: As a general rule there was one CCS per Division. It was found, though, that 10 CCSs were sufficient to treat the wounded in most major offensives. This allowed surplus CCSs to be employed for the reception of sick, infectious diseases, or special cases, such as head wounds, abdominal wounds, etc. In September 1916, every CCS was divided into a heavy and a light section. The light section was designed to be able to move forward or retire in line with the troops at a moment’s notice. A light section was also used to set up Advanced Operating Centres or Abdominal Hospitals. CCSs usually worked in groups of twos or threes, and in relay. This meant one would be closed and treating casualties for evacuation by train or ambulance to the Base Area, whilst the other would be empty and readying itself to receive new casualties. When the second one became full it would close, but the first would by now be empty and ready to receive new casualties again. A third would only be treating the sick, but would evacuate to receive battle casualties in an emergency. Each CCS took around 150 to 200 wounded before they closed and new patients arriving were redirected to another CCS. Early CCSs were established in buildings, but with the need for expansion, they began setting up on open ground, using tents and hospital Nissen huts. When on open ground they were situated near a railway siding for their own use, with a good road and communication towards the Front. The tents and huts provided accommodation for staff, and wounded, as well as operating theatres, medical and surgical stores, kitchens, sanitation, incineration plant, ablutions, and a mortuary. Portable generators were supplied to provide lighting. The conditions which determined the selection of sites for CCSs were: proximity to railways, good road approaches, reasonable security from hostile artillery fire, and adequate water supply. Capacity: Early CCSs were set up to provide accommodation for 200 patients, however the number of surgical operations being performed by 1917 meant they had expanded greatly, and were able to receive between 800 - 1,200 sick and wounded. Procedure: The standard system of receiving and treating casualties arriving at a CCS meant patients would go through: The stretcher exchange dump - where the drivers of motor ambulances delivered casualties and exchanged the equivalent of equipment handed in. A general admission tent or hut, or a receiving section - where a patient’s particulars were recorded in an Admission and Discharge (A & D) book, and his medical condition was classified by a medical officer. Refreshments such as tea, coffee, hot soup, sandwiches, and cigarettes were supplied here for waiting patients. A patient might then go to: A section for the dressing of walking patients: Here a patient might sit on benches, where he was attended to by a sister and/or orderlies working under a medical officer. A section for the dressing of lying down patients: Stretcher cases were carried here. If the patient’s wound was slight, it would be dressed, and the patient was then taken to the evacuation ward. If his wounds were more serious he was passed on to the pre-operation ward. A pre-operation section: Here the patient’s clothes were cut away, and he was cleansed, warmed and fed. A resuscitation ward: If on arrival the patient’s condition was too unstable for surgery, he was taken to the resuscitation ward, where a medical officer, a sister, and orderlies attended to his revivification. He was rested, warmed, infused or transfused - whichever might have been necessary. X-ray department: There were six mobile X-Ray units serving in the British Expeditionary Force during the Great War and these were sent to assist the CCS's during the great battles. Operating theatre: After 1916 there could be one or two theatres accommodating up to 12 tables arranged in pairs, each pair being divided from the other to provide privacy. Two tables were often provided for each team in order to save time. Surgical teams often worked in groups of 3 for 8 hours shifts with 4 hours off to sleep. This pattern could enable two operating tables to run continuously for a week. In reality, different CCSs worked in different ways. Major Richard Christopher Clarke R.A.M.C. of No 19 CCS stated that during one offensive “The surgeons were to do sixteen-hour shifts with eight hours off, thus giving us four tables going day and night.” Evacuation Section: After an operation, the patient could be carried here to await evacuation back to a Base Hospital. As stated above, slightly wounded were sent here after their wounds were dressed. Retention ward: If the patient was too ill to be evacuated, he was taken to a retention ward. These were situated at the back of the CCS in as quiet a place as possible. He was attended to here by the nurses and medical officers. Major Clarke provides a good insight into how the CCS’s procedure worked “The commanding officer was to be responsible for the administration and evacuation, and I was responsible for every case until operated on or marked for immediate evacuation.... In the theatre we had six tables, and the anaesthetist started the next case while the surgeon was dressing the last. Each surgeon had a sister and one trained orderly, and there was a free N.C.O and a free sister in the theatre to do sterilizing of instruments, etc. When it is realized that by this system no surgeon saw the case he was to operate on until he was under the anaesthetic, the proper selection of cases was of the utmost importance, and that is why we arranged that one man, myself, should stand the racket of any mistake. For this purpose in the dressing-room I had twelve tables to fit stretchers and twelve orderlies, one to each table, and a most efficient corporal in charge. Every case was brought in, put on the table, his wounds undone and a decision made, by me, as to his disposal, either to the resuscitation ward, to the pre-operation ward, to a ward especially kept for the dying, straight to one of the surgical wards or for immediate evacuation. My problem in a battle was to keep all the surgeons busy with cases really urgently needing operation. At the same time I had not to send so many to the pre-operating room that the last case would have to wait longer for his operation than if sent to the base; and, above all, not to send cases in for operation so badly wounded as to be unlikely to recover. It was a fairly difficult business, but by being kept informed of train times, by interviewing ambulance drivers and finding if more were to come, and being in and out of the pre-operation room and theatre, I was able to get a fair idea of the position.” [The Evolution of A Casualty Clearing Station on the Western Front - the presidential address, delivered on 14th October 1936, at the opening of the sixty-fourth session of the Bristol Medico-Chirurgical society.] Equipment: In 1914, there were no definite regulations limiting the amount of material and tentage which could be added to CCSs. Individual commanding officers requisitioned for whatever equipment they might consider necessary. However, it was recommended that every CCS have tents to accommodate 200 patients, 210 stretchers, 200 Paillasse cases, 200 bolster cases, 480 sheets, 50 feather pillows, 400 blankets, along with sufficient cooking and feeding utensils, medical stores and comforts, and surgical equipment. Surgical equipment comprised of: 1 small operating tent, 1 operating table, a few wooden splints, and a few yards of aluminum splinting. Doctors were encouraged to use local resources to obtain what they required. In June 1915, a further increase of equipment was authorized and CCSs were supplied with the ‘Bowlby Outfit No 2’. Later in the war small operating tents/areas were replaced by a Nissan hut of 60 feet in length and 20 feet in width - room for 4 operating tables and their equipment. Due to the vast expansion of CCSs, it became necessary to regulate the quantity of equipment allocated. The new scale equipment was issued in routine orders. Sets of equipment were kept in reserve at the Base Depot of Medical Stores in Boulogne and was sent up when required. This equipment list is far too large to state here but can be found in Volume II of the Medical Services General Official History and Volume I of the Medical Services Surgery of the War. Transport: There was no scale for transport laid down for the units in 1914 mobilization tables, but a footnote explained that if transport was required it would be furnished under the orders of the Inspector-General of communications. It was advised they should receive 17 general service wagons and 8 or 9 3-ton motor lorries when the unit was on the move. 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Many organizations are moving toward cloud-based services and infrastructure as to provide on-demand services. Many enterprises now use cloud-based computing platforms that allow services and data to be accessed over the Internet (or via other networks). Infrastructure providers of these cloud-based computing platforms offer network-based processing systems that often support multiple enterprises (or tenants) using common computer hardware and data storage. This “cloud” computing model allows applications to be provided over the network “as a service” supplied by the infrastructure provider. The infrastructure provider typically abstracts the underlying hardware and other resources used to deliver an enterprise-developed application so that the enterprise no longer needs to operate and support dedicated server hardware. The cloud computing model can often deliver substantial cost savings to the enterprise over the life of the application because the enterprise no longer needs to provide dedicated network infrastructure, electrical and temperature controls, physical security and other logistics in support of dedicated server hardware. A data center is a facility that centralizes an organization's IT operations and equipment, and where it stores, manages, and disseminates its data. A data center includes equipment, such as servers for IT operations and storage hardware for storage of an organization's data. Detecting failures of equipment that is used in such data centers is important to help ensure reliability. Cloud applications increasingly depend on large volumes of data, which requires multiple tiers of storage. Multiple tiers of storage can differ in terms of their cost, capacity, latency, reliability, and power consumption characteristics. These tiers can include memory, flash memory, single disk storage, redundant array of independent disks (RAID) based storage, network-attached storage (NAS) devices, and storage area networks (SAN). RAID storage is a data storage technology that provides a way of storing the same data redundantly in different places on multiple storage devices. These storage devices are typically hard disk drive storage devices or in some cases solid-state storage devices (SSDs). RAID storage can provide fault tolerance by combining multiple storage devices into a single logical unit, or array, so that data can be mirrored at each of the storage devices in the same array. This way, if one storage device fails the data is still preserved. RAID storage can also help improve overall performance, and increase storage capacity in a system. In a typical data center, RAID-based storage systems are indispensable due to their lower cost and higher volume.	3.125	3	[ 0.0093994140625, -0.01043701171875, -0.010986328125, 0.003936767578125, -0.01080322265625, -0.0205078125, -0.006011962890625, 0.00787353515625, 0.0040283203125, -0.006011962890625, -0.003173828125, -0.0024871826171875, 0.005859375, 0.0045166015625, -0.01519775390625, 0.00897216796875, -0.00092315673828125, 0.003448486328125, 0.000640869140625, 0.004638671875, 0.0126953125, 0.0081787109375, -0.0142822265625, 0.01422119140625, -0.00104522705078125, -0.00799560546875, 0.0059814453125, 0.003875732421875, -0.00003457069396972656, 0.006866455078125, 0.0037689208984375, -0.0037689208984375, -0.025390625, -0.01318359375, 0.009521484375, -0.0096435546875, 0.0002765655517578125, 0.00390625, -0.00101470947265625, -0.031005859375, -0.0034027099609375, -0.008544921875, -0.003173828125, 0.0087890625, -0.000888824462890625, -0.018310546875, 0.0086669921875, 0.004791259765625, 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Hydrogen is supplied to customers connected to a hydrogen pipeline system. Typically, the hydrogen is manufactured by steam methane reforming in which a hydrocarbon and steam are reacted at high temperature in order to produce a synthesis gas containing hydrogen and carbon monoxide. Hydrogen is separated from the synthesis gas to produce a hydrogen product stream that is introduced into the pipeline system for distribution to customers that are connected to the pipeline system. Alternatively, hydrogen produced from the partial oxidation of a hydrocarbon can be recovered from a hydrogen rich stream. Typically, hydrogen is supplied to customers under agreements that require availability and on stream times for the steam methane reformer or hydrogen recovery plant. When a steam methane reformer is taken off-line for unplanned or extended maintenance, the result could be a violation of such agreements. Additionally, there are instances in which customer demand can exceed hydrogen production capacity of existing plants. Having a storage facility to supply back-up hydrogen to the pipeline supply is therefore desirable in connection with hydrogen pipeline operations. Considering that hydrogen production plants on average have production capacities that are roughly 50 million standard cubic feet per day or greater, a storage facility for hydrogen that would allow a plant to be taken off-line, to be effective, would need to have storage capacity in the order of 1 billion standard cubic feet or greater. The large storage capacity can be met by means of salt caverns to store the hydrogen underground. Low purity grades of hydrogen (i.e., below 95% purity) as well as other gases have been stored in salt caverns. Salt caverns are large underground voids that are formed by adding fresh water to the underground salt, thus creating brine, which is often referred to as solution mining. Caverns are common in the gulf states of the United States where demand for hydrogen is particularly high. Such hydrogen storage has taken place where there are no purity requirements or less stringent (<96% pure) requirements placed upon the hydrogen product. In such case, the stored hydrogen from the salt cavern is simply removed from the salt cavern without further processing. High purity (e.g., 99.99%) hydrogen storage within salt caverns presents several challenges. For example, storing large quantities (e.g., greater than 100 million standard cubic feet) of pure (e.g., 99.99%) gaseous hydrogen in underground salt caverns consisting of a minimum salt purity of 75% halite (NaCl) or greater without measurable losses of the stored hydrogen is difficult based on the properties of hydrogen. Hydrogen is the smallest and lightest element within the periodic table of elements, having an atomic radius measuring 25 pm+/−5 pm. Further, hydrogen is flammable, and therefore a very dangerous chemical if not handled properly. Salt caverns consist of salt walls that have various ranges of permeability (e.g., 0-23×10^-6 Darcy) that if not controlled properly could easily allow gaseous hydrogen to permeate through the salt walls and escape to the surface of the formation. If the stored hydrogen within an underground salt formation was to escape and permeate through the salt formation to the surface, a dangerous situation could arise with fatality potential or immense structural damage potential. Consequently, high purity hydrogen is typically considered one of the most difficult elements to contain within underground salt formations. As will be discussed, among other advantages of the present invention, an improved method and system for storing hydrogen in a salt cavern is disclosed.	3.59375	4	[ -0.0123291015625, 0.0016021728515625, 0.0186767578125, -0.00102996826171875, -0.0242919921875, -0.034912109375, -0.003021240234375, -0.006103515625, -0.005126953125, 0.0128173828125, -0.00008869171142578125, 0.0031280517578125, -0.01483154296875, 0.0130615234375, -0.005523681640625, -0.00445556640625, -0.01153564453125, -0.01300048828125, 0.0166015625, -0.006744384765625, 0.03759765625, 0.00341796875, -0.00494384765625, 0.0038299560546875, 0.018798828125, 0.00091552734375, 0.00506591796875, -0.00016117095947265625, -0.01239013671875, 0.00146484375, 0.004150390625, 0.0093994140625, -0.0196533203125, -0.004608154296875, 0.00531005859375, -0.004638671875, 0.0084228515625, -0.00135040283203125, 0.0115966796875, -0.009521484375, -0.0074462890625, 0.005126953125, -0.0002002716064453125, -0.005126953125, -0.00823974609375, 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This image was degraded by the researchers to show what the old telescope would have seen. Credit: Big Bear Solar Observatory NJIT's new 1.6-meter clear aperture solar telescope—the largest of its kind in the world—is now operational. The unveiling of this remarkable instrument—said to be the pathfinder for all future, large ground-based telescopes—could not have come at a more auspicious moment for science. This year marks the 400th anniversary of Galileo's telescope that he used to demonstrate that sunspots are indeed on the Sun. "With our new big, beautiful white machine, Galileo's work can leap ahead with a capability never before available," said NJIT distinguished professor of physics Philip R. Goode. Goode, the heart and soul of the project, has been director of Big Bear Solar Observatory (BBSO), since NJIT took over management of BBSO in 1997 from California Institute of Technology. Located high above sea level in Big Bear Lake, CA, the observatory is one of six major land-based facilities supported by federal funding. This photo is the first light image from the new solar telescope at Big Bear Solar Observatory. Credit: Big Bear Solar Observatory "We are already seeing photos offering a better understanding of the Sun," said Goode. "With this instrument we should be able to have a better understanding of dynamic storms and space weather—which can have dramatic effects on Earth." Earlier this month, researchers achieved what is called first scientific light. This means the telescope is finally operational. To achieve its full powers, at least three more years of work will be needed. Photos from the first observations are still being processed. Nevertheless, Goode and his researchers were able to extract a few unique images and one is shown here. It clearly illustrates the before-and-after capabilities of the old versus new telescope. "Our prized first image shows the Sun's ever-present, turbulent granular field with its largest granules being about the size of Alaska," Goode said. "The small, bright points in the dark lanes are the smallest-scale magnetic structures on the Sun. Look closely at the "after" photo (which you may want to enlarge) and you will see a string of pearls. Each pearl is a cross-section of an intense, single fiber of the Sun's magnetic field - the basic building block of the solar magnetism." Goode adds that the Sun is now in a state of prolonged magnetic inactivity, perhaps the longest such time in a century. "The new telescope is ideal for studying the Sun as it rises from this strange state of quietude," he added. The new instrument has three times the aperture of the old telescope. It represents a significant advance in high-resolution observations of the Sun, since it has the largest aperture of any solar telescope in existence, said Goode. Other pluses include a marvelous location-- high in a Southern California mountain lake, and since it is an off-axis instrument, there is no part of sunlight blocked by the telescope, itself. The new telescope will be used in joint observation campaigns with NASA satellites to optimize the scientific output of all observations of the Sun. BBSO has always operated in such campaigns, but now can do so with greatly-enhanced capabilities. The National Science Foundation (NSF), Air Force Office of Special Research (AFOSR) and NASA have provided more than $5 million in hardware components. The telescope is filled with new technologies. The 1.7-meter (equivalent to 4.6 feet) primary mirror was polished by the world-renowned Steward Observatory Mirror Laboratory at the University of Arizona (UA). The extremely-precise measurements of the mirror's shape required the application, for the first time, of a computer-generated hologram. The development of this technology will be essential for figuring the next generation of even-larger night time telescopes. The final error in the primary mirror is only a few parts in a billion from its desired parabolic shape. "Buddy Martin at the UA Mirror Lab has described the mirror in ours as the pathfinder for large nighttime telescopes that are about-to-be built," said Goode. This is the new solar telescope at Big Bear Solar Observatory. Credit: Big Bear Solar Observatory Another key design issue for this large-aperture solar telescope was the creation of a thermal control system capable of maintaining the temperature of the mirrors near or below ambient air. To achieve this, the dome employs a wind-gate and exhaust system which controls the airflow from the wind. The structure maintains the same temperature inside and outside the dome, and clears concentrations of heat in and around the optical paths. In addition, BBSO engineers implemented a closed-cycle, chilled-air system as part of the telescope mount to limit so-called "mirror seeing." This sweeps away turbulent cells and directly cools the primary mirror. After a day of observations, the mirror must be cooled overnight to ensure that it is somewhat cooler than ambient in the morning. DFM Engineering, Longmont, CO, built and tested the optical support structure and active-support mirror cell for the enormous mirror. It is supported by 36 actuators that can bend out low-order aberrations, such as those due to gravity and/or thermal effects. The telescope is now in its commissioning phase in which more sophisticated observations are made possible with the implementation of advanced hardware. These include adaptive optics to correct for atmospheric distortion and hardware to measure magnetic fields in visible and infrared light. "It is good at last to have our destiny in our own hands rather than those of our capable partners," said Goode. "Seeing first light was a great moment because the team in BBSO finally knew that its big white machine works as we had planned." 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Introduction {#sec1} ============ Since December 2019, several cases of pneumonia of unknown etiology have been reported in Wuhan, Hubei Province, of China.[@bib1] Those cases have been confirmed as acute respiratory infections caused by a novel coronavirus infection. To date, confirmed cases have been found in many countries worldwide.[@bib2] ^,^ [@bib3] Until now, however, the source of the virus and the pathogenesis of the disease are unknown. Early detection, quarantine, and timely treatment are the keys to better controlling the epidemic and reducing the spread of the disease. Coronaviruses are RNA viruses and can be divided into 4 genera according to the genomic characteristics: α, β, γ, and ξ.[@bib4] Among these, Middle East respiratory syndrome coronavirus and severe acute respiratory syndrome coronavirus are known coronaviruses.[@bib4] ^,^ [@bib5] The new virus recently discovered in China is now recognized to be a novel coronavirus named 2019-nCoV. The coronavirus isolated from patients with this novel pneumonia in Wuhan is a coronavirus of genus β.[@bib5] This sudden infectious disease mainly manifests as fever, fatigue, and cough.[@bib6], [@bib7], [@bib8] Upper respiratory symptoms such as nasal congestion and runny nose are rare. About one half of the patients develop dyspnea after 1 week.[@bib9] In severe cases, patients progress rapidly to acute respiratory distress syndrome (ARDS), sepsis, and coagulopathy. Some patients have mild symptoms with no fever or without pneumonia and usually recover after 1 week. However, some patients may suddenly worsen and develop ARDS.[@bib9] At present, how to stratify high-risk and low-risk patients is an important but unresolved issue. In the present study, the clinical manifestations and clinical outcomes of patients with 2019 novel coronavirus disease (COVID-19) were evaluated. The purpose of this study was to identify the risk factors associated with pneumonia, ARDS, and clinical outcomes. Patients and methods {#sec2} ==================== Patients {#sec2.1} -------- This cross-sectional multicenter clinical study was approved by the institutional ethics board of the Nanfang Hospital, Southern Medical University. All consecutive patients with confirmed 2019-nCoV infections who were diagnosed in the Dongguan People\'s Hospital and Nanfang Hospital, Southern Medical University, from January 2020 to February 2020 were enrolled. The study population comprised hospitalized patients. Because COVID-19 is an infectious disease, all outpatients were required to be quarantined in the hospital if infection with 2019-nCoV was confirmed. The 2019-nCoV infection diagnostic standard was polymerase chain reaction detection of 2 target genes of 2019-nCoV, open reading frame 1 ab (ORF1ab) and nucleocapsid protein. A positive result was determined to be 2019-nCoV infection. Ethics, Consent, and Permissions {#sec2.2} -------------------------------- The Institutional Review Board of Nanfang Hospital, Southern Medical University, approved this study. All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation and with the 1975 Declaration of Helsinki as revised in 2008. Oral consent was obtained from patients. Data Collection {#sec2.3} --------------- All patients\' clinical, laboratory, and radiologic characteristics, as well as treatment outcome data, were obtained through medical record extraction. Data were reviewed by a team of trained physicians. The recorded information included demographic data, medical history, contact history, potential comorbidities, symptoms, laboratory test results, and chest computed tomography (CT) scans. ARDS was defined as an acute-onset oxygenation index (arterial partial pressure of oxygen/fraction of inspired oxygen) ≤ 300 mm Hg and a chest radiograph showing patchy shadows.[@bib10] Real-Time Polymerase Chain Reaction Assay for 2019-nCoV {#sec2.4} ------------------------------------------------------- All patients had pharyngeal swab samples collected to detect 2019-nCoV. The specific steps were as follows: The throat swab was placed into a collection tube containing 150 μL of virus preservation solution, and a respiratory sample RNA isolation kit (Zhongzhi, Wuhan, China) was used to extract total RNA within 2 h. Forty microliters of cell lysate were transferred to a collection tube and vortexed for 10 s. It was centrifuged after incubation at room temperature for 10 min. Real-time polymerase chain reaction was then performed, and 2 target genes (ORF1ab and nucleocapsid protein) were detected. Target 1 (ORF1ab): forward primer CCTGGTGGGTTTTACACTTAA; reverse primer ACGATTGTGCATCAGCTGA; probe 5′-VIC-CCGTCTGCGGTATGTGGAAAGGTTATGG-BHQ1-3′. Target 2 (N protein): forward primer GGGGAACTTCTCCTGCTAGAAT; reverse primer CAGACATTTTGCTCTCAAGCTG; probe 5′-FAM-TTGCTGCTGCTTGACAGATT-TAMRA-3′. The diagnostic criteria were based on the recommendations of the National Institute of Viral Disease Prevention and Control (<http://ivdc.chinacdc.cn/kyjz/202001/t20200121_211337.html>). Statistical Analysis {#sec2.5} -------------------- Continuous data are reported as mean (SD), and categorical data are expressed as percentages. The significance of differences was tested by using either the Student\'s t test (for continuous variables) or the χ2 test (for categorical variables). Univariable and multivariable regression analyses were performed by using logistic regression analysis, and the results are expressed as odds ratio (OR) and 95% CIs. All analyses were performed by using SPSS version 13.0 (IBM SPSS Statistics, IBM Corporation, Armonk, New York) with an alpha level of 0.05. Results {#sec3} ======= Characteristics of Patients With COVID-19 {#sec3.1} ----------------------------------------- A total of 95 patients infected with 2019-nCoV were enrolled. Seventy-three had pneumonia based on the CT findings, and 22 did not have pneumonia. Demographic and clinical characteristics are shown in [Table I](#tbl1){ref-type="table"} . Patients with pneumonia were significantly older than the other patients (p \< 0.001). The body mass index (BMI) (p = 0.001), aspartate aminotransferase levels (p = 0.041), and lactate dehydrogenase (LDH) levels (p = 0.003) were significantly higher in patients with pneumonia. However, lymphocyte count (p = 0.014) and platelet count (p \< 0.001) were significantly lower in patients with pneumonia.Table IDemographic and clinical characteristics in patients with coronavirus disease 2019 (COVID-19) with or without pneumonia. Values are givens as mean (SD) unless otherwise indicated.Table ICharacteristicPatients With COVID-19PWith PneumoniaWithout PneumoniaSample size, n7322--Male sex39 (53.4%)14 (63.6%)0.398Age, y42.66 (17.93)23.86 (13.88)\<0.001SBP, mm Hg126.41 (16.01)120.95 (14.90)0.175DBP, mm Hg83.69 (10.26)79.90 (8.60)0.138BMI, kg/m^2^23.71 (3.41)20.78 (3.15)0.001Serum lactic acid, mmol/L1.51 (0.71)1.61 (0.59)0.608Neutrophil count, × 10^9^3.32 (1.52)3.33 (1.29)0.972Lymphocyte count, × 10^9^1.25 (0.94)1.81 (0.87)0.014Hemoglobin, g/L139.07 (18.07)143.41 (13.01)0.298Platelet count, × 10^9^196.27 (56.67)251.50 (77.46)\<0.001Serum creatinine, μmol/L68.60 (41.11)60.95 (17.97)0.400ALT, U/L21.33 (12.00)22.77 (24.75)0.718AST, U/L23.97 (10.48)18.75 (7.72)0.041LDH, IU/L204.04 (67.44)154.32 (34.88)0.003Tobacco smoking5 (6.8%)3 (13.6%)0.315[^2] Univariate and Multivariate Analyses of Factors Associated With Pneumonia {#sec3.2} ------------------------------------------------------------------------- Univariate and multivariate analyses were conducted to analyze the risk factors associated with 2019-nCoV--infected patients developing pneumonia. Univariate results showed that older age, high BMI, low lymphocyte count, low platelet count, high aspartate aminotransferase level, and high LDH level were risk factors associated with patients developing pneumonia. However, multivariate analysis showed that only older age (OR, 1.078; p = 0.008) and high BMI (OR, 1.327; p = 0.024) were independent risk factors associated with patients developing pneumonia ([Table II](#tbl2){ref-type="table"} ).Table IIFactors associated with pneumonia in patients with coronavirus disease 2019.Table IIVariableUnivariate AnalysisMultivariate AnalysisOR95% CIPOR95% CIPSex0.6550.245--1.7510.400Age1.0731.034--1.112\<0.0011.0781.020--1.1400.008SBP1.0230.990--1.0570.176DBP1.0400.987--1.0950.141BMI1.2981.103--1.5270.0021.3271.038--1.6970.024Serum lactic acid0.8150.376--1.7650.603Neutrophil count0.9940.717--1.3780.972Lymphocyte count0.5480.305--0.9860.045Hemoglobin0.9860.959--1.0130.301Platelet count0.9870.979--0.9950.002Serum creatinine1.0110.986--1.0360.387ALT0.9940.965--1.0250.716AST1.0801.001--1.1650.048LDH1.0231.007--1.0390.004Tobacco smoking0.4660.102--2.1270.324[^3] Differences in Characteristics Between the ARDS Group and the Non-ARDS Group {#sec3.3} ---------------------------------------------------------------------------- Using the ARDS definition, patients were divided into an ARDS group (n = 24) and a non-ARDS group (n = 71) ([Table III](#tbl3){ref-type="table"} ). Patients with ARDS were older than those without ARDS (p = 0.021). Moreover, systolic blood pressure (SBP) (p = 0.038), serum creatinine (p = 0.025), and LDH (p = 0.003) levels were significantly higher in patients with ARDS. However, lymphocyte counts were lower in patients with ARDS than in others (p = 0.046).Table IIIThe demographic and clinical characteristics in patients with coronavirus disease 2019 (COVID-19) with and without acute respiratory distress syndrome (ARDS). Values are given as mean (SD) unless otherwise indicated.Table IIICharacteristicPatients With COVID-19PWith ARDSWithout ARDSSample size, n2471--Male sex14 (58.3%)39 (54.9%)0.772Age, y45.92 (18.44)35.73 (13.32)0.021SBP, mm Hg130.96 (14.62)123.15 (15.87)0.038DBP, mm Hg84.92 (10.42)82.12 (9.93)0.245BMI, kg/m^2^24.26 (3.32)22.64 (3.55)0.053Serum lactic acid, mmol/L1.49 (0.51)1.55 (0.74)0.703Neutrophil count, × 10^9^3.21 (1.34)3.36 (1.51)0.656Lymphocyte count, × 10^9^1.05 (0.48)1.49 (1.04)0.046Hemoglobin, g/L141.46 (12.47)139.61 (18.41)0.648Platelet count, × 10^9^193.67 (67.23)214.27 (65.15)0.187Serum creatinine, μmol/L81.42 (65.91)61.90 (18.02)0.025ALT, U/L23.83 (14.07)20.91 (16.05)0.439AST, U/L25.49 (11.68)21.92 (9.48)0.146LDH, IU/L228.86 (80.21)181.79 (55.17)0.003Tobacco smoking1 (4.2%)7 (9.9%)0.385[^4] Univariate and Multivariate Analyses of Factors Associated With ARDS {#sec3.4} -------------------------------------------------------------------- Logistic regression was used to identify factors that were significantly associated with ARDS in patients with COVID-19. In multivariate analysis, high SBP level (OR, 1.046; p = 0.025) and high LDH level (OR, 1.010; p = 0.021) were found to be independent risk factors associated with ARDS among patients with COVID-19 ([Table IV](#tbl4){ref-type="table"} ).Table IVFactors associated with acute respiratory distress syndrome in patients with coronavirus disease 2019.Table IVVariableUnivariate AnalysisMultivariate AnalysisOR95% CIPOR95% CIPSex1.1490.450--2.9300.772Age1.0311.004--1.0580.025SBP1.0331.001--1.0660.0421.0461.006--1.0890.025DBP1.0290.981--1.0790.244BMI1.1470.996--1.3200.057Serum lactic acid0.8650.416--1.8010.699Neutrophil count0.9270.665--1.2920.652Lymphocyte count0.3590.141--0.9180.032Hemoglobin1.0060.980--1.0340.645Platelet count0.9950.987--1.0030.188Serum creatinine1.0210.995--1.0480.116ALT1.0110.983--1.0400.443AST1.0330.988--1.0800.154LDH1.0111.003--1.0180.0071.0101.001--1.0190.021Tobacco smoker0.3980.046--3.4080.400[^5] Differences in Characteristics Between Patients With Pneumonia Exacerbation and Relief {#sec3.5} -------------------------------------------------------------------------------------- A total of 70 patients underwent CT scanning repeatedly after 1 week of treatment. Based on the findings obtained after comparison with the first CT scan, patients were divided into the pneumonia exacerbation group (n = 19) and the pneumonia relief group (n = 51). The characteristics were compared, and the results showed that patients with pneumonia exacerbation were significantly older (p = 0.021), with a higher BMI (p = 0.003) and a higher proportion of tobacco smokers (p = 0.006) ([Table V](#tbl5){ref-type="table"} ).Table VDemographic and clinical characteristics in patients with coronavirus disease 2019 (COVID-19) with pneumonia exacerbation or relief.Table VCharacteristicPatients with COVID-19PPneumonia ExacerbationPneumonia ReliefSample size, n1951--Male sex11 (57.9%)24 (47.1%)0.420Age, y49.58 (22.16)38.37 (15.80)0.021SBP, mm Hg127.63 (13.11)125.39 (17.43)0.614DBP, mm Hg81.26 (10.95)84.14 (10.58)0.322BMI, kg/m^2^25.38 (2.49)22.95 (3.61)0.003Serum lactic acid, mmol/L1.53 (0.75)1.56 (0.72)0.896Neutrophil count, × 10^9^3.47 (1.62)3.29 (1.58)0.679Lymphocyte count, × 10^9^1.13 (0.58)1.31 (1.05)0.481Hemoglobin, g/L139.68 (13.46)137.92 (19.83)0.722Platelet count, × 10^9^184.95 (50.78)207.19 (60.51)0.159Serum creatinine, μmol/L81.74 (73.92)61.76 (17.34)0.073ALT, U/L19.38 (11.03)21.78 (12.55)0.477AST, U/L23.26 (12.71)23.80 (10.05)0.856LDH, IU/L201.16 (80.15)200.40 (64.92)0.968Tobacco smoking4 (21.1%)1 (2.0%)0.006[^6] Univariate and Multivariate Analyses of Factors Associated With Pneumonia Exacerbation {#sec3.6} -------------------------------------------------------------------------------------- Logistic regression was used to identify factors that were associated with pneumonia exacerbation in patients with COVID-19. Multivariate analysis showed that a high BMI (OR, 1.285; p = 0.017) and tobacco smoking (OR, 16.13; p = 0.032) were independent risk factors associated with 2019-nCoV--infected patients with pneumonia exacerbation after treatment ([Table VI](#tbl6){ref-type="table"} ).Table VIFactors associated with pneumonia exacerbation in patients with coronavirus disease 2019.Table VIVariableUnivariate AnalysisMultivariate AnalysisOR95% CIPOR95% CIPSex1.5470.534--4.4820.422Age1.0371.004--1.0710.026SBP1.0090.976--1.0420.608DBP0.9740.926--1.0250.319BMI1.2531.049--1.4970.0131.2851.045--1.5810.017Serum lactic acid0.9490.440--2.0470.894Neutrophil count1.0720.774--1.4850.674Lymphocyte count0.7460.325--1.7140.490Hemoglobin1.0050.977--1.0340.718Platelet count0.9930.983--1.0030.161Serum creatinine1.0140.990--1.0390.244ALT0.9820.936--1.0310.472AST0.9950.945--1.0480.854LDH1.0000.992--1.0080.967Tobacco smoking6.6671.110--40.040.03816.131.275--204.160.032[^7] Discussion {#sec4} ========== The present study found that older age and high BMI were independent risk factors associated with patients with pneumonia. Furthermore, high SBP level and high LDH level were independent risk factors associated with ARDS among patients with COVID-19. High BMI and tobacco smoking were independent risk factors associated with pneumonia exacerbation after treatment in patients with COVID-19. These results help in the risk stratification of patients with COVID-19. Timely intervention should be initiated in patients with risk factors to avoid disease progression. In addition, the results of this study may have implications for the pathogenesis of COVID-19. Most patients with COVID-19 will develop pneumonia.[@bib11] However, a small proportion of patients have negative radiographic findings. The largest study sample to date showed that among the 3665 confirmed cases, 95.5% (n = 3498) of patients were diagnosed with pneumonia.[@bib12] According to the Diagnosis and Treatment Program of 2019 New Coronavirus Pneumonia recommended by The National Health Commission of China, these patients only exhibited low fever and mild fatigue with no pneumonia manifestations, and they usually recovered after 1 week. Our study confirmed these results. We found that some patients had negative CT scan results, although the throat swabs confirmed infection with 2019-nCoV. Most previous studies were conducted in Wuhan Province with patients enrolled from Wuhan, and the symptoms of those first-generation patients were relatively severe. The patients enrolled in the present study were from Guangdong Province, which is not the first generation of infected patients. In our study, the patients' symptoms were relatively mild, which is in line with the results of patients from Zhejiang Province.[@bib13] Symptoms of patients outside Hubei Province are relatively mild. Some 2019-nCoV--infected patients will rapidly become critically ill.[@bib9] ^,^ [@bib14] Previous research reported that the mortality rate of 2019-nCoV--infected patients is 4%--15%.[@bib7] ^,^ [@bib9] In our study, only one patient aged 75 years (BMI, 29.37 kg/m^2^) died (mortality rate, 1.05%). Therefore, early detection of this population is very important. However, this subpopulation of patients who have severe disease may have moderate to low fever in the development of the disease. It is still difficult to screen out these patients. Our research may provide a sign. According to the results of our study, the 2019-nCoV--infected patients who developed ARDS were older and had higher SBP, serum creatinine, and LDH levels. This group of people also had lower lymphocyte counts. However, multivariate analysis suggested that only high SBP level and high LDH level were independent risk factors associated with ARDS among patients with COVID-19. Previous research implied that some patients' conditions will change dramatically in \~1 week.[@bib9] In our study, we performed repeated CT examinations on 70 patients after 1 week of treatment and found that those with imaging findings suggesting exacerbations had clinical baseline data significantly different from patients with reduced disease. Tobacco smoking has been confirmed to be associated with many diseases.[@bib15] ^,^ [@bib16] In our study, multivariate analysis suggests that high BMI and tobacco smoking were independent risk factors associated with disease exacerbation in 2019-nCoV--infected patients after treatment. Until now, there have been no antiviral drugs specifically approved for treating 2019-nCoV--infected patients. Although reports have suggested the potential antiviral effects of lopinavir/ritonavir, it remains controversial.[@bib14] Remdesivir has shown strong potential antiviral effects in previous reports but has not yet been approved by the US Food and Drug Administration, and large clinical research results are lacking to support its application.[@bib2] ^,^ [@bib17] Finding an effective treatment plan is a particularly important clinical problem. The present study discusses the evolution of CT findings for patients with COVID-19. However, CT scans are not frequently used for assessment of patients with complicated pneumonia or ARDS. CT scan findings cannot completely identify exacerbation or relief of the disease. The CT scan results can only reflect some aspects in the development of the disease. The findings from our study may not have clinical relevance across different parts of the world. This study has limitations. First, it involved a cross-sectional investigation. Second, the relative sample size was limited. The potential limitations of the present report could be overcome in future studies by enrolling more patients. In our study, there was no control group, and there was no comparator virus-infected group. Most of these findings are the same as would be seen with influenza, respiratory syncytial virus, and human metapneumovirus. The results from our study may imply that high-risk patients are at high risk of complications because of who they are (their specific characteristics), and not because of the specific nature of the individual pathogen. The airway inflammation coupled with their clinical factors is the real issue. In addition, prognostic outcomes were assessed. In the present study, all patients diagnosed with ARDS were admitted to the intensive care unit to continue further treatment. However, other prognostic outcomes, including length of stay data, in this study are missing because some patients are still in the hospital. Further study is needed to determine mortality and length of stay data. Conclusions {#sec5} =========== Older age and high BMI were independent risk factors associated with pneumonia in patients with COVID-19. High SBP and LDH levels were independent risk factors associated with ARDS, whereas high BMI and tobacco smoking were independent risk factors associated with disease exacerbation after treatment. For such patients, stratification by using independent risk factors could help with the management of their disease. Disclosures =========== The authors have indicated that they have no conflicts of interest regarding the content of this article. This work was supported by grants from the 10.13039/501100013076Major Science and Technology Special Project of China (2017ZX09304016, 2017ZX10302201004008). The authors thank Jian Zhang for his helpful assistance in the study. Drs. S. Cai, Yin, Xu, and Peng designed and guided the study; Drs. S. Cai and Yu wrote the main manuscript text; and Drs. Zheng, Liu, and X. Cai prepared all tables and data analysis. All authors reviewed the manuscript. [^1]: These authors contributed equally to this work. [^2]: ALT = alanine aminotransferase; AST = aspartate aminotransferase; BMI = body mass index; DBP = diastolic blood pressure; LDH = lactate dehydrogenase; SBP = systolic blood pressure. [^3]: ALT = alanine aminotransferase; AST = aspartate aminotransferase; BMI = body mass index; DBP = diastolic blood pressure; LDH = lactate dehydrogenase; OR = odds ratio; SBP = systolic blood pressure. [^4]: ALT = alanine aminotransferase; AST = aspartate aminotransferase; BMI = body mass index; DBP = diastolic blood pressure; LDH = lactate dehydrogenase; SBP = systolic blood pressure. [^5]: ALT = alanine aminotransferase; AST = aspartate aminotransferase; BMI = body mass index; DBP = diastolic blood pressure; LDH = lactate dehydrogenase; OR = odds ratio; SBP = systolic blood pressure. [^6]: ALT = alanine aminotransferase; AST = aspartate aminotransferase; BMI = body mass index; DBP = diastolic blood pressure; LDH = lactate dehydrogenase; SBP = systolic blood pressure. 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Reducing Risks to Women Linked to Shift Work, Long Work Hours, and Related Workplace Sleep and Fatigue Issues. In the United States, an estimated 12% to 28% of working women are on shift work schedules, and 12% work more than 48 hours per week. Shift work and long work hours are associated with many health and safety risks, including obesity, injuries, and negative reproductive outcomes. Over time, the worker is at risk for developing a wide range of chronic diseases. These work schedules can also strain personal relationships, owing to fatigue and poor mood from sleep deprivation and reduced quality time to spend with family and friends. Worker errors from fatigue can lead to reduced quality of goods and services, negatively impacting the employer. In addition, mistakes by fatigued workers can have far-reaching negative effects on the community, ranging from medical care errors to motor vehicle crashes and industrial disasters that endanger others. To reduce the many risks that are linked to these demanding work hours, the National Institute for Occupational Safety and Health (NIOSH) conducts research, develops guidance and authoritative recommendations, and translates and disseminates scientific information to protect workers, their families, employers, and the community. The key message to reduce these risks is making sleep a priority in the employer's systems for organizing work and in the worker's personal life. The NIOSH website has freely available online training programs with suggestions for workers and their managers to help them better cope with this workplace hazard.	3.078125	3	[ 0.0033416748046875, -0.00171661376953125, 0.01708984375, -0.015869140625, -0.004791259765625, -0.0164794921875, 0.00168609619140625, -0.0159912109375, 0.0098876953125, -0.027587890625, 0.00787353515625, 0.006317138671875, -0.01171875, 0.00543212890625, -0.00579833984375, 0.00152587890625, 0.0015716552734375, 0.003753662109375, -0.00335693359375, 0.00567626953125, 0.01080322265625, 0.017333984375, -0.00115966796875, 0.006195068359375, -0.0022125244140625, 0.007537841796875, -0.01397705078125, 0.00439453125, 0.00537109375, -0.01263427734375, 0.000865936279296875, -0.0169677734375, -0.021728515625, -0.003936767578125, 0.00341796875, -0.01556396484375, 0.00164031982421875, -0.005615234375, 0.00159454345703125, 0.033935546875, -0.00982666015625, -0.0081787109375, -0.0028076171875, 0.000873565673828125, 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Hydrated alkali metal silicates are known fire-proofing materials and are extensively employed in building construction. Under the high temperatures existing during a fire, the water of hydration is driven off causing the composition to puff, expanding by up to 25 to 40 times its original volume. Thus, when combined with fire-stop materials these materials intumesce to provide a layer of insulation against fire and smoke, said layer being full of bubbles and holes from the expansion of the water of hydration. The foaming pressure helps to seal apertures and passages in building structures making these fireproofing materials useful in fire-stops, see U.S. Pat. No. 4,364,210. Alkali metal silicates can also be incorporated into proofing materials such as asphalt shingles in order to convert these shingles into a fire retardant Class A or B form. Alkali metal silicate particles may be placed in an asphalt layer in between the top layer of asphalt and roofing granules and the substrate of organic felt or fiberglass mat. In the event of a fire on a roof, the intumescent silicate particles expand to form a thermal barrier which retards ignition of the roofing deck. The formation of alkali metal silicate gels by the addition of such materials as sodium aluminate or boric acid solutions to alkali metal silicates at elevated temperatures is known (see U.S. Pat. No. 4,297,252, Example 3, and U.S. Pat. No. 3,498,807, column 3, lines 42-56). It is also known that the production of a solid, hydrated alkali metal silicate in which the moisture content is controlled can require carefully controlled drying conditions (see U.S. Pat. No. 3,895,995). Typically, alkali metal silicate suspensions or gels described in the literature are dried or cured at temperatures ranging from 90.degree. to 136.degree. C. and below the boiling point of the suspension or solution. One difficulty with silicate based materials is their degradation on exposure to water or high relative humidity for extended periods of time. Water is known to leach away the alkali metal oxide from the silicate particles, reducing their ability to intumesce. Various solutions to this problem have been proposed in the past, including a coating which covers alkali metal silicate particles (see U.S. Pat. No. 4,218,502). it is the object of this invention to provide an alkali metal silicate material which retains its intumescence after long exposure to water in order to ensure that its effectiveness as a fire protection agent will last a long time under outdoor weathering conditions.	3.109375	3	[ -0.01190185546875, -0.005096435546875, 0.0157470703125, -0.004547119140625, -0.0029449462890625, -0.0181884765625, 0.00799560546875, 0.0189208984375, 0.00133514404296875, 0.00421142578125, -0.00469970703125, 0.00689697265625, -0.01153564453125, -0.00775146484375, -0.0177001953125, 0.00579833984375, -0.0069580078125, 0.003814697265625, -0.00113677978515625, -0.00180816650390625, 0.052978515625, 0.00136566162109375, -0.00482177734375, 0.01446533203125, 0.012939453125, -0.002197265625, 0.0081787109375, 0.0012359619140625, 0.0079345703125, 0.0159912109375, -0.0078125, -0.005615234375, -0.022216796875, 0.00506591796875, -0.006744384765625, -0.01104736328125, -0.0003871917724609375, 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Northern Gully This Mars Global Surveyor (MGS) Mars Orbiter Camera (MOC) image shows a gully formed in the wall of a north middle-latitude crater. Similar gullies are common at the middle and polar latitudes of Mars, and might have formed by the action of liquid water. Others have argued for carbon dioxide or dry mass movement for the genesis of such landforms. This particular image was acquired during northern autumn, when the sky over the terrain of the martian northern mid-latitudes is typically hazy. MGS MOC Release No. MOC2-1234, 28 September 2005	3.09375	3	[ -0.005523681640625, -0.0028076171875, 0.0030059814453125, 0.003448486328125, 0.00799560546875, -0.01953125, -0.00921630859375, -0.01611328125, 0.00616455078125, -0.01434326171875, 0.0208740234375, 0.0033416748046875, -0.0311279296875, 0.01397705078125, -0.0038909912109375, -0.0118408203125, -0.01251220703125, 0.010009765625, -0.0009918212890625, -0.01165771484375, -0.02880859375, -0.005523681640625, 0.0128173828125, -0.0079345703125, 0.004547119140625, 0.00762939453125, 0.006683349609375, -0.025634765625, -0.01904296875, -0.000385284423828125, -0.00063323974609375, -0.0113525390625, -0.00872802734375, -0.032958984375, -0.00555419921875, 0.0120849609375, -0.0189208984375, 0.00213623046875, -0.013671875, -0.01202392578125, 0.0159912109375, 0.007537841796875, 0.0150146484375, -0.0018768310546875, -0.0203857421875, 0.00179290771484375, 0.013671875, 0.018310546875, 0.00138092041015625, 0.006683349609375, 0.0019989013671875, 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Primary Menu PCB Making: 2. Get Started This is a step of looking for an idea or the purpose of what a board should be doing. You will likely know what you need and then build a suitable board. I needed to build something useful so I can look forward to it once it was done: I wanted to be able to interact with it but also use parts that I already have at home. In my parts bin, I found a fairly standard LCD display that I got with an Arduino board. It can display 16 characters in 2 rows. This should be a good display device to use. A couple of push-buttons are definitely a must for any interactivity as well as a few LEDs: can’t do without mandatory blinking lights! Digging through my parts I’ve found a DS18B20 temperature sensor, a simple 1-Wire device, so I added it in. Bins with various parts I wanted to use the Atmel SAM3N1 CPU which I already ordered from DigiKey. This quite powerful MCU needs a JTAG to program it. The MCU has a number of built in peripherals including an UART (“serial port”) so I also wanted to use those pins to communicate through the serial interface. After adding needed parts in the power supply circuitry, pin headers, test pins and so on, I felt that was complex enough for the scope of this project. Bins and bags of parts The final rough idea for a board quickly took shape: it should have a couple of buttons for user interaction, it should display temperature read from a sensor and to make it more interesting, display a random fortune (do you remember that old ‘fortune’ Unix application?).	3	3	[ 0.0025177001953125, 0.0010986328125, 0.00347900390625, -0.01214599609375, -0.002593994140625, 0.003631591796875, -0.006256103515625, 0.000507354736328125, -0.0162353515625, -0.000400543212890625, 0.005523681640625, 0.006744384765625, -0.007049560546875, 0.0106201171875, 0.001007080078125, -0.00127410888671875, -0.0023040771484375, 0.006317138671875, 0.00032806396484375, 0.0186767578125, 0.0458984375, -0.0203857421875, -0.01019287109375, 0.006561279296875, 0.01324462890625, -0.00616455078125, -0.0033721923828125, 0.009033203125, 0.010498046875, -0.016357421875, 0.0014495849609375, 0.00958251953125, -0.0269775390625, -0.017578125, 0.00616455078125, 0.01953125, 0.007232666015625, 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Q: What is wrong with this code that calculates areas, please? (Python) Hello, I am new to python. And I do not know why this code does not work: def area_finder_rectangle (height,width): area = heightwidth print("The area of your polygon is %.2f" % area) def area_finder_triangle (height,width): area = (heightwidth)0.5 print("The area of your polygon is %.2f" % area) while True: print ("Choose the polygon that you want to calculate the area from.") print ("Polygons supported: rectangle, triangle") value = str(input("Your polygon is a: ")) print ("Be sure to include decimals even if you are going to input an integer") if value == "rectangle" or "Rectangle": heightt = float(input("Enter height: ")) widthh = float(input("Enter width: ")) area_finder_rectangle (height = heightt,width = widthh) elif value == "triangle" or "Triangle": heightt = float(input("Enter height: ")) widthh = float(input("Enter width: ")) area_finder_triangle (height = heightt,width = widthh) print ("") When you choose rectangle is just fine, but when you choose triangle, this happens: >>> Choose the polygon that you want to calculate the area from. Polygons supported: rectangle, triangle Your polygon is a: triangle Be sure to include decimals even if you are going to input an integer Enter height: 10 Enter width: 10 The area of your polygon is 100.00 A: if value == "rectangle" or "Rectangle": is not what you think it is. It will compare value with the complete result of the expression "rectangle" or "Rectangle" which will always evaluate to True. It should be like this: if value == "rectangle" or value == "Rectangle": But a better option is if value.lower() == "rectangle": Or even better, convert to lowercase directly at the input. value = str(input("Your polygon is a: ")).lower() Sidenote: If you want to compare a value with several values, you can do like this: if value in ["rectangle", "Rectangle", "RECTANGLE"]: But in this case that's not an optimal option. Just convert to lowercase before comparing. Here is complete code: def area_finder_rectangle (height,width): area = heightwidth print("The area of your polygon is %.2f" % area) def area_finder_triangle (height,width): area = (heightwidth)0.5 print("The area of your polygon is %.2f" % area) while True: print ("Choose the polygon that you want to calculate the area from.") print ("Polygons supported: rectangle, triangle") value = str(input("Your polygon is a: ")).lower() print ("Be sure to include decimals even if you are going to input an integer") if value == "rectangle": heightt = float(input("Enter height: ")) widthh = float(input("Enter width: ")) area_finder_rectangle (height = heightt,width = widthh) elif value == "triangle": heightt = float(input("Enter height: ")) widthh = float(input("Enter width: ")) area_finder_triangle (height = heightt,width = widthh) print ("") And a testrun: [klutt@klutt-sandbox tmp]# python3 polygon.py Choose the polygon that you want to calculate the area from. Polygons supported: rectangle, triangle Your polygon is a: rectangle Be sure to include decimals even if you are going to input an integer Enter height: 10.0 Enter width: 10.0 The area of your polygon is 100.00 Choose the polygon that you want to calculate the area from. Polygons supported: rectangle, triangle Your polygon is a: triangle Be sure to include decimals even if you are going to input an integer Enter height: 10.0 Enter width: 10.0 The area of your polygon is 50.00 One thing you should consider, which in this case would have made it easier for you to discover the problem, is to always add an else in case of non-valid input. if value == "rectangle": <do something> elif value == "triangle": <do something> else: print("Unknown polygon") A: Your branch if value == "rectangle" or "Rectangle:" will always be taken and you will always calculate a rectangle. Why it does this makes more sense if you put in parentheses. if (value == "rectangle") or ("Rectangle"): If value is 'triangle' the first part evaluates to False but the second part of the or-condition evaluates to True since in Python a non-empty string in a boolean context is considered True. To get the effect you want you need to say if (value == "rectangle") or (value == "Rectangle"):	3.3125	3	[ -0.01483154296875, -0.0267333984375, 0.0244140625, 0.00008916854858398438, 0.00689697265625, 0.00604248046875, -0.01123046875, -0.004486083984375, -0.0089111328125, 0.012939453125, 0.01373291015625, -0.0166015625, -0.0419921875, 0.0031585693359375, -0.0029754638671875, -0.0240478515625, 0.00023365020751953125, -0.005767822265625, -0.00189971923828125, -0.0216064453125, 0.0732421875, 0.0120849609375, -0.01373291015625, 0.016845703125, -0.00119781494140625, -0.021240234375, 0.0179443359375, 0.0078125, 0.0211181640625, -0.0019989013671875, 0.005279541015625, -0.004669189453125, -0.030517578125, -0.000598907470703125, 0.01190185546875, 0.0145263671875, 0.007293701171875, 0.02099609375, -0.0018463134765625, -0.0025787353515625, -0.01556396484375, -0.0152587890625, 0.02880859375, 0.00653076171875, -0.002166748046875, 0.0017547607421875, -0.01220703125, -0.000518798828125, -0.013671875, 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All relevant data are within the paper and its Supporting Information files. Introduction {#sec001} ============ The brain size of humans has increased dramatically during the evolution of Homo sapiens, along with the acquisition of uniquely human features, such as language, memory, self-awareness, creativity, and social communication \[[@pone.0179624.ref001]--[@pone.0179624.ref005]\]. Elucidating the similarities and differences in the ontogeny of brain structures between humans and our closest living primate relatives, chimpanzees, is important to understand the unique features of the human brain. The corpus callosum (CC) is the major commissural white matter bundle that connects the left and right cerebral hemispheres and provides interhemispheric integration, which is related to sensory, motor, and higher-order cognitive functions \[[@pone.0179624.ref006], [@pone.0179624.ref007]\]. The CC is present in all primates and has evolved with the neocortex \[[@pone.0179624.ref008], [@pone.0179624.ref009]\]. The CC exhibits a topographic pattern of the different cortical areas \[[@pone.0179624.ref007], [@pone.0179624.ref010], [@pone.0179624.ref011]\], which is associated with different regions: the rostrum; genu; rostral body; and the anterior midbody connect regions of the prefrontal and frontal cortex; the posterior midbody connects the region of the somatosensory cortex; the isthmus connects regions of the parietal and superior temporal cortex; and the splenium connects the occipital, inferior temporal, and parietal regions \[[@pone.0179624.ref012]--[@pone.0179624.ref017]\]. This topographic relationship is similar in humans and chimpanzees \[[@pone.0179624.ref018]\]. The midsagittal area of the CC has been commonly used as a sensitive marker of brain development and maturation \[[@pone.0179624.ref019]--[@pone.0179624.ref023]\], since the CC area is related to number of axons and morphology, such as axon diameter and myelination \[[@pone.0179624.ref024]--[@pone.0179624.ref028]\]. In humans, midsagittal CC areas increase rapidly during the first two to three years of life (corresponds to infancy: note that the anthropological definition \[[@pone.0179624.ref029]--[@pone.0179624.ref036]\], which is different from the medical definition, is adopted in this report. See the Section "Definitions of developmental stages" for details) \[[@pone.0179624.ref037], [@pone.0179624.ref038]\] and continue to increase slowly during the juvenile stage, adolescence \[[@pone.0179624.ref021]--[@pone.0179624.ref023], [@pone.0179624.ref038]--[@pone.0179624.ref040]\], and young adulthood, until the third decade of life \[[@pone.0179624.ref019], [@pone.0179624.ref021], [@pone.0179624.ref041], [@pone.0179624.ref042]\]. In chimpanzees, a cross-sectional magnetic resonance imaging (MRI) study of the ages from 6 to 54 years (corresponds to the end of the juvenile stage to old age) indicated a gradual increase in the CC areas during this age-range, which was similar to that seen in humans. The only exception was found in the rostrum subdivision of the CC, with no significant increase during this age range \[[@pone.0179624.ref043]\]. Since the study did not include chimpanzees that were less than six years of age \[[@pone.0179624.ref043]\], whether there is a rapid increase in CC areas during infancy in chimpanzees, such as that seen in humans, is still unknown. How the rostrum develops during infancy is of particular interest, since the developmental trajectory after the juvenile stage in chimpanzees is different from that seen in humans. To investigate the developmental changes during infancy and the juvenile stage of the chimpanzee CC, we longitudinally quantified areas of the midsagittal total CC and the CC subdivisions of four chimpanzees from 1.8 months to six years of age (infancy to the juvenile stage), using MRI, and compared the results with those of humans. Materials and methods {#sec002} ===================== Participants {#sec003} ------------ ### Chimpanzees {#sec004} Four chimpanzees (one male and three females), whose ages ranged from 1.8 to 72 months, were longitudinally evaluated during development from infancy to the juvenile stage ([S1 Table](#pone.0179624.s003){ref-type="supplementary-material"}). In addition, ten adult chimpanzees were cross-sectionally evaluated as references ([S1 Table](#pone.0179624.s003){ref-type="supplementary-material"}). Adult chimpanzee characteristics were as follows: mean (s.d.) age, 31.2 (5.8) years; female/male ratio 30 percent male. All subjects lived within a social group of 14 individuals in an enriched environment with a 700-m^2^ outdoor compound enhanced by 15-m-high climbing frames and about 500 planted trees of approximately 60 species \[[@pone.0179624.ref044]\], as well as an attached indoor residence at the Primate Research Institute, Kyoto University (KUPRI) \[[@pone.0179624.ref045], [@pone.0179624.ref046]\]. Access to the outdoor compound was available to all chimpanzees every other day during the day. Daily meals included a wide variety of fresh fruits and vegetables fed throughout the day, supplemented with nutritionally balanced biscuits (fed twice daily) and water available ad libitum. The treatment of the chimpanzees was in accordance with the 2002 and 2010 version of the Guidelines for the Care and Use of Laboratory Primates issued by KUPRI. All care and experimental protocols were approved by the Animal Welfare and Animal Care Committee of the KUPRI. Of note, one of the longitudinally-followed chimpanzees had spinal cord compression due to osteogenesis imperfecta at the T8-T11 level of the thoracic vertebrae and had paraplegia and chronic renal dysfunction. She died from pneumonia at the age of two years. The disabled infant chimpanzee was raised by her biological mother in the social group. The caretakers and veterinarians closely monitored the mother and the infant, and provided the necessary care and treatments to minimize the suffering of the chimpanzee, in accordance with the Guidelines for the Care and Use of Laboratory Primates of the KUPRI. There were neither any symptoms suggesting brain abnormality nor noticeable MRI abnormalities of the brain. ### Humans {#sec005} We used part of the previously published numerical dataset from a human cross-sectional MRI study about midsagittal CC areas. Seventy-two healthy children (40 males, 32 females), whose ages ranged from one month to 126 months (see details in \[[@pone.0179624.ref038]\]), were analyzed ([S1 Table](#pone.0179624.s003){ref-type="supplementary-material"}). The comparison with human adult CC areas was based on the data from 14 healthy adults who served as controls \[[@pone.0179624.ref038]\]. Adult participant characteristics were as follows: mean (s.d.) age, 19.9 (1.9) years; female/male ratio, 50 percent male ([S1 Table](#pone.0179624.s003){ref-type="supplementary-material"}). All parents and adult participants gave written, informed consent for participation after the nature and possible consequences of the study were explained. All the protocols of the study were approved by the Committee on Medical Ethics of Toyama University (\#165). Image acquisition {#sec006} ----------------- ### Chimpanzees {#sec007} Three-dimensional, T1-weighted, whole-brain images were acquired with a 0.2 Tesla MR imager (Signa Profile; General Electric). The image data from three longitudinally evaluated chimpanzees (Ayumu, Cleo, and Pal) were acquired at the following time points: 6, 12, 24, 36, 48, 60, and 72 months. Another longitudinally evaluated chimpanzee (Pico) was scanned at the following time points: 1.8, 3, 4, 6, 9, and 24 months. The chimpanzees were anesthetized with ketamine (3.5 mg/kg) and medetomidine (0.035 mg/kg), and remained anesthetized with additional ketamine (1.75 mg/kg) and/or inhalation of isoflurane or sevoflurane as needed during the scans (total time anesthetized, approximately two hours). After the scans, they were reversed with atipamezole (0.175 mg/kg) and temporarily housed in a single home cage for recovery. During the scans, the chimpanzees were placed in the scanner chamber in a supine position with their heads fitted inside either the extremity coil (for the longitudinally evaluated chimpanzees) or the head coil (for the adult chimpanzees). For the four longitudinally-evaluated chimpanzees and four of the adult chimpanzees, a three-dimensional spoiled gradient-recalled acquisition in steady state (SPGR) sequence was obtained with the following acquisition parameters: repetition time (TR), 46 ms; echo time (TE), 10 ms; flip angle, 60°; slice thickness. 1.0--2.0 mm; field of view, 20--24 cm; matrix size, 256 × 256; number of excitations, two. For the other adult chimpanzees, a three-dimensional fast gradient echo with inversion recovery prep (FGRE-IrP) sequence was obtained with the following acquisition parameters: repetition time (TR), 32.3 ms; echo time (TE), 8.5 ms; flip angle, 40°; slice thickness, 1.5 mm; field of view, 24 cm; matrix size, 256 × 256; number of excitations, two. ### Humans {#sec008} The acquisition sequence and scan procedures of the human scan have been detailed in a previous publication \[[@pone.0179624.ref038]\]. Briefly, three-dimensional, T1-weighted, whole human-brain images were acquired with a 1.5 Tesla MR imager (Magnetom Vision; Siemens) using the fast low angle shot three-dimensional gradient refocused (GRE) sequence. The acquisition parameters were: repetition time (TR), 35 ms; echo time (TE), 6 ms; flip angle, 35°; slice thickness, 1.5 mm; field of view, 25.6 cm; matrix size, 256 × 256; number of excitations, one. Image processing {#sec009} ---------------- ### Total CC and CC subdivisions {#sec010} The midsagittal CC areas of the MRI for each individual were analyzed using Analyze 9.0 software (Mayo Clinic, Mayo Foundation, Rochester, MN, USA) in the following series of semi-manual procedures. (i) All images were converted into cubic voxel dimensions of 0.55 mm using a cubic spline interpolation algorithm. (ii) Brain image volumes were realigned to a standard anatomical orientation, with the transaxial plane parallel to the anterior commissure-posterior commissure line and perpendicular to the interhemispheric fissure. (iii) The midsagittal CC area measurements were obtained from the midsagittal slice in accordance with a method described by Witelson's studies \[[@pone.0179624.ref047], [@pone.0179624.ref048]\] and previous neuroimaging studies \[[@pone.0179624.ref022], [@pone.0179624.ref038], [@pone.0179624.ref043]\]. (iv) This method divides the total midsagittal CC area into the subdivisions of rostrum, genu, rostral body, anterior midbody, posterior midbody, isthmus, and splenium ([Fig 1](#pone.0179624.g001){ref-type="fig"}). To subdivide the total midsagittal CC area, the entire length of the total midsagittal CC area was first measured, and then divided into thirds. The anterior third was further divided into three regions by tracing a vertical line through the point where the anterior CC area began to curve back slightly. This resulted in three subdivisions: the rostrum; the genu; and the rostrum body. The middle third of the overall CC area was subdivided into equal sections, resulting in the anterior midbody and posterior midbody. Finally, the posterior third of the overall CC area was subdivided into the isthmus and splenium. The splenium was defined as the posterior fifth of the entire CC area; the remaining area within the posterior third was defined as the isthmus. Using the tracing tool, the area of the CC lying within each outlined region was measured in each individual. ![Regional subdivisions of the chimpanzee corpus callosum from a midsagittal view.\ The total CC midsagittal area was divided into seven equally spaced subdivisions: 1 = rostrum (red); 2 = genu (green); 3 = rostral body (yellow); 4 = anterior midbody (blue); 5 = posterior midbody (magenta); 6 = isthmus (cyan); 7 = splenium (white).](pone.0179624.g001){#pone.0179624.g001} Two evaluators (T.S. and K.O.), who were blinded to the sex and age of the subjects, semi-manually traced and measured the midsagittal CC areas. The intra-rater and inter-rater reproducibility of the CC measurements used in this study were evaluated. Ten brain scans were randomly selected for analysis. An analysis of intra-rater reproducibility was conducted using two sets of the brain measurements obtained by T.S. The inter-rater reproducibility was analyzed by comparing brain measurements obtained by T.S. and K.O. The Pearson's correlation coefficients for the comparisons of the results were r = 0.98 (intra-rater) and r = 0.97 (inter-rater), which indicated good reliability of the manual quantification. ### Normalization of the total CC and the CC subdivisions relative to adult areas {#sec011} To account for differences in the CC areas between adult chimpanzees and adult humans, the total CC and the CC subdivisions were normalized based on the average CC area of adult brains, and demonstrated as a percentage of adult areas (normalized area, hereafter). Since the ages of the adult chimpanzees tended to be older than that of adult humans, we investigated the effects of age on areas of total CC and the CC subdivisions in these two adult groups using a linear regression model. Total CC and the CC subdivisions served as the dependent variables. Age was introduced as an independent variable. There were no significant age-dependent changes in total CC or the CC subdivisions in either species ([S2 Table](#pone.0179624.s004){ref-type="supplementary-material"}). Therefore, we concluded that the adult chimpanzees and adult humans were comparable to serve as the adult control groups, given that their callosal measures were stable with respect to age. Definitions of developmental stages {#sec012} ----------------------------------- In chimpanzees, the developmental stages were defined as follows: "infancy" corresponded to \~12 months of age, and the "juvenile stage" corresponded to \~84 months of age; in humans, these designations corresponded to \~24 months of age and \~144 months of age, respectively. The developmental stages were applied based on previous publications that used the first eruption of the first deciduous tooth \[[@pone.0179624.ref031], [@pone.0179624.ref032]\], weight increase \[[@pone.0179624.ref029], [@pone.0179624.ref034]\], and sexual maturation (menarche, first ejaculation) \[[@pone.0179624.ref030], [@pone.0179624.ref033], [@pone.0179624.ref035], [@pone.0179624.ref036]\]. The longitudinally evaluated chimpanzees of this study were observed to undergo sexual maturation at the age of seven years. Statistical analysis {#sec013} -------------------- We investigated subdivision-specific developmental trajectories in each species. For the chimpanzee study, the MRIs were obtained longitudinally from four young chimpanzees from 1.8 to 72 months of age. For the human study, MRIs were obtained from 72 children between the ages of one month and 126 months, using a cross-sectional design. These differences in study design and number of participants made the cross-species statistical comparison difficult. Therefore, we decided to remain descriptive in highlighting the similarities and differences between chimpanzees and humans, as previously reported \[[@pone.0179624.ref049]--[@pone.0179624.ref051]\]. ### Developmental trajectories of the total CC and the subdivisions {#sec014} The relationships between the age and the CC areas were investigated by polynomial regression analyses. F-tests were used to determine whether the order of a developmental model was cubic, quadratic, or linear. First, linear, quadratic, or cubic polynomial regression models were fitted by age using R.v. 3.2.2 software to identify the developmental patterns in the total CC and the CC subdivisions. If a cubic model did not yield significant results, a quadratic model was tested; if a quadratic model did not yield significant results, a linear model was tested. Thus, a growth model was polynomial/nonlinear if either the cubic or quadratic term significantly contributed to the regression equation. The Akaike information (a log-likelihood function) \[[@pone.0179624.ref052]\] was used to ensure effective model selection. Second, using R.v. 3.2.2 software, the data that showed nonlinear trajectories were fitted by locally weighted polynomial regression (LOESS) \[[@pone.0179624.ref053]\]. In this way, even with relatively few data points, the age-related area size changes could be delineated by applying the curve-fitting suggested by previous human studies \[[@pone.0179624.ref054], [@pone.0179624.ref055]\] and chimpanzee studies \[[@pone.0179624.ref049]--[@pone.0179624.ref051]\], without enforcing a common parametric function on the dataset, as is the case with linear polynomial models. For the fit at age X, the fit is made using values in the neighborhood of X, each weighted by the distance from X. The size of the neighborhood is defined by alpha. Data were fitted in four interactions with alpha = 0.70, in accordance with previous MRI studies \[[@pone.0179624.ref049]--[@pone.0179624.ref051], [@pone.0179624.ref055]\]. The observed and fitted values of the total CC and the CC subdivisions were plotted as a function of age to display the age-related change. The analysis was performed on the original CC areas as well as on the normalized CC areas (% of adult area, as described in the Section "Normalization of the total CC and the CC subdivisions relative to adult areas"). ### Difference in normalized areas among CC subdivisions {#sec015} We investigated the differences between the normalized areas among the CC subdivisions. This was motivated by a previous chimpanzee MRI study that indicated that there was no increase in the rostrum area in chimpanzees after the juvenile stage, while other subdivisions still developed \[[@pone.0179624.ref043]\]. This suggested that each subdivision has specific developmental features, and the features are potentially species-specific. Since the study design (longitudinal vs. cross-sectional) and the number of participants (four chimpanzees vs. 72 humans) were different between the two species, we applied different statistical methods for each species. For the longitudinal dataset of the young chimpanzees, the nonparametric one-way analysis of variance (ANOVA) with repeated measures (Friedman test) (η ^2^ and p values) was applied to investigate within-group differences among the seven CC subdivisions. The CC subdivisions served as the test variables. When the Friedman test yielded a significant effect (p \< 0.05), a post hoc analysis was performed using a Dunn\'s test for nonparametric pairwise comparisons between assessments, with a Bonferroni correction applied, resulting in a significance level set at p \< 0.05. For the cross-sectional dataset of the young humans, the parametric one-way ANOVA with repeated measures (F and p values) was applied to investigate within-group differences among the seven CC subdivisions. The CC subdivisions served as the within-subjects variables. Age was a covariate. When the parametric one-way ANOVA with repeated measures yielded a significant effect (p \< 0.05), a post hoc analysis was performed using a paired t-test for parametric pairwise comparisons between assessments, with a Bonferroni correction applied, resulting in a significance level set at p \< 0.05. Results {#sec016} ======= Evaluation of the developmental trajectory of the total CC and the subdivisions {#sec017} ------------------------------------------------------------------------------- ### Chimpanzees {#sec018} Overall, the results of the total CC and the CC subdivisions revealed noteworthy developmental changes in chimpanzees throughout the study period (1.8 to 72 months) ([Fig 2](#pone.0179624.g002){ref-type="fig"}, Tables [1](#pone.0179624.t001){ref-type="table"}, [2](#pone.0179624.t002){ref-type="table"} and [3](#pone.0179624.t003){ref-type="table"}, and [S1 Table](#pone.0179624.s003){ref-type="supplementary-material"}). The total CC followed a nonlinear developmental trajectory (F = 50.99, cubic effect, p = 2.55×10^−10^) ([Table 3](#pone.0179624.t003){ref-type="table"}). All of the CC subdivisions also increased nonlinearly (rostrum, F = 23.39, cubic effect, p = 3.58×10^−7^; genu, F = 57.56, cubic effect, p = 7.56×10^−11^; rostral body, F = 11.73, cubic effect, p = 7.31×10^−5^; anterior midbody, F = 25.51, cubic effect, p = 1.69×10^−7^; posterior midbody, F = 22.02, cubic effect, p = 5.98×10^−7^; isthmus, F = 25.29, cubic effect, p = 1.83×10^−7^; splenium, F = 27.31, quadratic effect, p = 3.17×10^−6^) ([Table 3](#pone.0179624.t003){ref-type="table"}). LOESS scatter plots for the area of the total CC and the subdivisions (in mm^2^) are demonstrated in [Fig 3](#pone.0179624.g003){ref-type="fig"}, and the normalized total CC and the subdivisions (in %) are demonstrated in [Fig 4](#pone.0179624.g004){ref-type="fig"}. ![An ontogenetic series of the regional subdivisions of the chimpanzee corpus callosum from a midsagittal view.\ Regional subdivisions: 1 = rostrum (red); 2 = genu (green); 3 = rostral body (yellow); 4 = anterior midbody (blue); 5 = posterior midbody (magenta); 6 = isthmus (cyan); 7 = splenium (white). The bars below the figures indicate the developmental stage. The indicated developmental stages are infancy (open bar), the juvenile stage (hatched bar), and the adult stage (horizonal striped bar).](pone.0179624.g002){#pone.0179624.g002} ![Evaluation of the corpus callosum areas during development.\ Age-related changes in the total CC and the CC subdivisions during infancy and the juvenile stage are shown for chimpanzees (n = 4) and humans (n = 72). (A) total, (B) rostrum, (C) genu, (D) rostral body, (E) anterior midbody, (F) posterior midbody, (G) isthmus, and (H) splenium. The bar below the graphs indicates the developmental stage. The indicated developmental stages are infancy (open bar) and the juvenile stage (hatched bar).](pone.0179624.g003){#pone.0179624.g003} ![Evaluation of the normalized corpus callosum areas during development.\ Age-related changes in the total CC and the CC subdivisions relative to the adult areas during infancy and the juvenile stage are shown for chimpanzees (n = 4) and humans (n = 72). (A) total, (B) rostrum, (C) genu, (D) rostral body, (E) anterior midbody, (F) posterior midbody, (G) isthmus, and (H) splenium. The bar below the graphs indicates the developmental stage. The indicated developmental stages are infancy (open bar) and the juvenile stage (hatched bar).](pone.0179624.g004){#pone.0179624.g004} 10.1371/journal.pone.0179624.t001 ###### Sample characteristics of the corpus callosum areas in chimpanzees. ![](pone.0179624.t001){#pone.0179624.t001g} ---------------------------------------------------------- -------- ------- Infants (age≤12 mons) (Number of scans = 11) Region Median IQR Total CC 134.60 55.02 Rostrum 4.79 2.99 Genu 22.43 13.75 Rostral body 23.93 8.37 Anterior midbody 18.54 5.69 Posterior midbody 14.95 3.89 Isthmus 11.07 3.89 Splenium 33.20 17.64 Juveniles (12 mons \<age≤84 mons) (Number of scans = 16) Region Median IQR Total CC 204.72 45.23 Rostrum 7.18 2.31 Genu 48.30 2.99 Rostral body 32.45 10.54 Anterior midbody 23.33 4.49 Posterior midbody 21.39 6.06 Isthmus 16.45 5.01 Splenium 50.55 18.99 ---------------------------------------------------------- -------- ------- Month, mon; interquartile range, IQR. Area size characteristics of the sample classified into subgroups according to developmental stage. In chimpanzee scans (Longitudinal scan, n = 4), values represent median and IQR measured area (mm^2^). 10.1371/journal.pone.0179624.t002 ###### Sample characteristics of the corpus callosum areas relative to adult areas (normalized areas) in chimpanzees. ![](pone.0179624.t002){#pone.0179624.t002g} ---------------------------------------------------------- -------- ------- Infants (age≤12 mons) (Number of scans = 11) Region Median IQR Total CC 40.70 16.64 Rostrum 46.97 29.32 Genu 31.70 19.43 Rostral body 43.35 15.16 Anterior midbody 42.55 13.06 Posterior midbody 37.62 9.78 Isthmus 39.13 13.74 Splenium 40.02 21.27 Juveniles (12 mons \<age≤84 mons) (Number of scans = 16) Areas Median IQR Total CC 61.90 13.67 Rostrum 70.41 22.70 Genu 68.26 4.23 Rostral body 58.78 19.08 Anterior midbody 53.54 10.30 Posterior midbody 58.14 17.69 Isthmus 60.93 22.90 Splenium 61.90 13.67 ---------------------------------------------------------- -------- ------- Month, mon; interquartile range, IQR. Area size characteristics of the sample classified into subgroups according to developmental stage. In chimpanzee scans (Longitudinal scan, n = 4), values represent median and IQR normalized area of the adult area (%). 10.1371/journal.pone.0179624.t003 ###### Results of polynomial regression modeling of the developmental trajectories of the corpus callosum areas. ![](pone.0179624.t003){#pone.0179624.t003g} Species Region Best fitting model F R^2^ sig ------------------- ----------- -------------------- ------- ---------------- ---------------- Chimpanzees Total CC Cubic 50.99 0.85 2.55×10^−10^ Rostrum Cubic 23.39 0.72 3.58×10^−7^ Genu Cubic 57.56 0.87 7.56×10^−11^ Rostral body Cubic 11.73 0.55 7.31×10^−5^ Anterior midbody Cubic 25.51 0.74 1.69×10^−7^ Posterior midbody Cubic 22.02 0.71 5.98×10^−7^ Isthmus Cubic 25.29 0.74 1.83×10^−7^ Splenium Quadratic 27.31 0.67 3.17×10^−6^ Humans Total Cubic 86.42 0.78 \<2.20×10^−16^ Rostrum Cubic 7.50 0.22 2.08×10^−4^ Genu Cubic 73.64 0.75 \<2.20×10^−16^ Rostral body Cubic 25.94 0.51 2.67×10^−11^ Anterior midbody Cubic 69.56 0.74 \<2.20×10^−16^ Posterior midbody Cubic 59.62 0.71 \<2.20×10^−16^ Isthmus Cubic 36.71 0.60 3.18×10^−14^ Splenium Cubic 52.42 0.68 \<2.20×10^−16^ Age-related changes in the total CC and the CC subdivisions in chimpanzees (n = 4) and in humans (n = 72). F = F value, R^2^ = adjusted R^2^ value. "Best fitting model," "F," "R^2^," and "sig" indicate the results of the statistical analysis of the age-related changes in the total CC and the CC subdivisions with a polynomial regression model. The best-fitting model represents the best-fitting model of the linear, quadratic, and cubic regression models. ### Humans {#sec019} As observed in chimpanzees, the results of the total CC and the CC subdivisions revealed noteworthy developmental changes in humans through the study period (one month to 126 months) ([Fig 2](#pone.0179624.g002){ref-type="fig"}, Tables [3](#pone.0179624.t003){ref-type="table"}, [4](#pone.0179624.t004){ref-type="table"} and [5](#pone.0179624.t005){ref-type="table"}, and [S1 Table](#pone.0179624.s003){ref-type="supplementary-material"}). The total CC followed a nonlinear developmental trajectory (F = 86.42, cubic effect, p \< 2.20×10^−16^) ([Table 5](#pone.0179624.t005){ref-type="table"}). All of the CC subdivisions also increased nonlinearly (rostrum, F = 7.50, cubic effect, p = 2.08×10^−4^; genu, F = 73.64, cubic effect, p \< 2.20×10^−16^; rostral body, F = 25.94, cubic effect, p \< 2.67×10^−11^; anterior midbody, F = 69.56, cubic effect, p \< 2.20×10^−16^; posterior midbody, F = 59.62, cubic effect, p \< 2.20×10^−16^; isthmus, F = 36.71, cubic effect, p = 3.18×10^−14^; and splenium, F = 52.42, quadratic effect, p \< 2.20×10^−16^) ([Table 5](#pone.0179624.t005){ref-type="table"}). LOESS scatter plots for the area of the total CC and the subdivisions (in mm^2^) are demonstrated in [Fig 3](#pone.0179624.g003){ref-type="fig"}, and the normalized total CC and the subdivisions (in %) are demonstrated in [Fig 4](#pone.0179624.g004){ref-type="fig"}. 10.1371/journal.pone.0179624.t004 ###### Sample characteristics of the corpus callosum areas in humans. ![](pone.0179624.t004){#pone.0179624.t004g} ----------------------------------------------------------- -------- -------- Infants (age≤24 mons) (Number of scans = 36) Region Mean SD Total CC 309.64 109.87 Rostrum 10.084 5.32 Genu 67.53 32.06 Rostral body 53.83 16.91 Anterior midbody 34.28 13.24 Posterior midbody 30.64 10.56 Isthmus 21.75 7.87 Splenium 91.53 33.98 Juveniles (24 mons \<age≤144 mons) (Number of scans = 36) Region Mean SD Total CC 481.11 92.75 Rostrum 14.75 5.08 Genu 111.7 16.95 Rostral body 71.14 13.38 Anterior midbody 53.06 10.50 Posterior midbody 48.92 8.75 Isthmus 38.17 8.08 Splenium 143.42 28.50 ----------------------------------------------------------- -------- -------- Month, mon; standard deviation, SD. Area size characteristics of the sample classified into subgroups according to developmental stage. In human scans (Cross-sectional scan, n = 72), values represent mean and SD normalized area of the adult area (%). 10.1371/journal.pone.0179624.t005 ###### Sample characteristics of the corpus callosum areas relative to adult areas (normalized areas) in humans. ![](pone.0179624.t005){#pone.0179624.t005g} ----------------------------------------------------------- ------- ------- Infants (age≤24 mons) (Number of scans = 36) Region Mean SD Total CC 51.83 18.39 Rostrum 47.05 24.80 Genu 49.45 23.49 Rostral body 62.70 19.69 Anterior midbody 51.60 30.48 Posterior midbody 49.88 17.19 Isthmus 44.32 16.03 Splenium 51.82 19.24 Juveniles (24 mons \<age≤144 mons) (Number of scans = 36) Region Mean SD Total CC 80.53 8.94 Rostrum 68.83 23.70 Genu 81.76 12.41 Rostral body 82.86 15.59 Anterior midbody 79.87 10.62 Posterior midbody 79.63 11.30 Isthmus 77.78 16.46 Splenium 81.19 11.35 ----------------------------------------------------------- ------- ------- Month, mon; standard deviation, SD. Area size characteristics of the sample classified into subgroups according to developmental stage. In human scans (Cross-sectional scan, n = 72), values represent mean and SD measured area (mm^2^). Evaluation of regional variation in normalized areas among CC subdivisions {#sec020} -------------------------------------------------------------------------- ### Chimpanzees {#sec021} The nonparametric Friedman test indicated a significant main effect of the normalized subdivision areas (η ^2^ = 25.94, P = 2.29×10^−4^). Post hoc tests using a Dunn\'s test showed that the area of the rostrum differed significantly from that of the anterior midbody (P = 0.003), the posterior midbody (P = 0.002), and the isthmus (P = 0.007) ([Table 6](#pone.0179624.t006){ref-type="table"}). The LOESS curves of the normalized CC subdivisions indicated that the increase was most rapid in the rostrum, compared to the other CC subdivisions, and the area reached close to 100% of the adult area by the end of the juvenile stage ([Fig 4B--4H](#pone.0179624.g004){ref-type="fig"}). 10.1371/journal.pone.0179624.t006 ###### Differences in normalized areas among CC subdivisions in chimpanzees. ![](pone.0179624.t006){#pone.0179624.t006g} ------------------- ----------------- ------- -------------- ------------------ ------------------- --------- ---------- Rostrum Genu Rostral body Anterior midbody Posterior midbody Isthmus Splenium Rostrum Genu 1.000 Rostral body 1.000 1.000 Anterior midbody [.003]{.ul} 1.000 .294 Posterior midbody [.002]{.ul} 1.000 .247 1.000 Isthmus [.007]{.ul} 1.000 .557 1.000 1.000 Splenium .064 1.000 1.000 1.000 1.000 1.000 ------------------- ----------------- ------- -------------- ------------------ ------------------- --------- ---------- Values present Bonferroni-corrected P values. Underlined bold characters indicate a significant difference between CC subdivisions. ### Humans {#sec022} The parametric one-way repeated measures ANOVA indicated a significant main effect of subdivisions (F = 6.98, P = 4.4E-07). There was a significant interaction for age-by-subdivisions (F = 3.77, P = 0.001). Post hoc tests using a paired t-test showed that the area of the rostral body differed significantly from that of the rostrum (P = 7.0E-07), the genu (P = 0.004), the anterior midbody (P = 2.0E-04), the posterior midbody (P = 4.1E-04), the isthmus (P = 2.6E-06), and the splenium (P = 1.4E-03) ([Table 7](#pone.0179624.t007){ref-type="table"}). The LOESS curves of the normalized CC subdivisions indicated that the area of the rostral body was greater than that of the other CC subdivisions at the onset of infancy, and the area reached more than 80% of the adult area by the end of infancy ([Fig 4B--4H](#pone.0179624.g004){ref-type="fig"}). 10.1371/journal.pone.0179624.t007 ###### Differences in normalized areas among CC subdivisions in humans. ![](pone.0179624.t007){#pone.0179624.t007g} ------------------- -------------------- ----------------- -------------------- ------------------ ------------------- --------- ---------- Rostrum Genu Rostral body Anterior midbody Posterior midbody Isthmus Splenium Rostrum Genu .286 Rostral body [7.0E-07]{.ul} [.004]{.ul} Anterior midbody .164 1.000 [2.0E-04]{.ul} Posterior midbody .500 1.000 [4.1E-04]{.ul} 1.000 Isthmus 1.000 .582 [2.6E-06]{.ul} .168 .560 Splenium .077 1.000 [1.4E-03]{.ul} 1.000 1.000 .050 ------------------- -------------------- ----------------- -------------------- ------------------ ------------------- --------- ---------- Values present Bonferroni-corrected P values. Underlined bold characters indicate a significant difference between CC subdivisions. Descriptive comparison of developmental trajectories of the total CC between chimpanzees and humans {#sec023} --------------------------------------------------------------------------------------------------- ### Similarities between chimpanzees and humans {#sec024} There were two noticeable similarities. First, the total CC increased rapidly during infancy and continued to increase slowly during the juvenile stage in both species ([Fig 4A](#pone.0179624.g004){ref-type="fig"}). Second, the normalized total CC at the beginning of infancy was similarly small in both species. It was 25% in chimpanzees and 31% in humans ([Fig 4A](#pone.0179624.g004){ref-type="fig"}). ### Differences between chimpanzees and humans {#sec025} There were two noticeable differences between chimpanzees and humans. First, although the total CC increased rapidly during infancy in both species, the slope was steeper in humans than in chimpanzees. The total CC of the chimpanzees increased 220% during infancy, while the increase was 238% in humans ([Fig 3A](#pone.0179624.g003){ref-type="fig"}). Second, at the end of the juvenile stage, the normalized total CC of humans was greater than that of chimpanzees. In humans, the normalized area reached 85% at the end of the juvenile stage, while it remained at 71% in chimpanzees ([Fig 4A](#pone.0179624.g004){ref-type="fig"}). Descriptive comparison of developmental trajectories of the CC subdivisions between chimpanzees and humans {#sec026} ---------------------------------------------------------------------------------------------------------- ### Similarities between chimpanzees and humans {#sec027} There were three noticeable similarities between chimpanzees and humans. First, the proportion of each CC subdivision was similar between the two species. In adult chimpanzees, the areas of the rostrum, genu, rostral body, anterior midbody, posterior midbody, isthmus, and the splenium were 3, 21, 17, 13, 12, 9, and 25% of the total CC, respectively ([S1 Table](#pone.0179624.s003){ref-type="supplementary-material"}). The corresponding values for humans were 4, 23, 14, 11, 10, 8, and 30% of the total, respectively ([S1 Table](#pone.0179624.s003){ref-type="supplementary-material"}). Second, the relative area of the CC subdivisions at the beginning of infancy was similar in both species, except for the rostral body (detailed in the Section "Differences between chimpanzees and humans"). In chimpanzees, the normalized CC subdivision areas at the beginning of infancy were 31% in the rostrum, 19% in the genu, 29% in the anterior midbody, 27% in the posterior midbody, 27% in the isthmus, and 25% in the splenium ([Fig 4B, 4C and 4E--4H](#pone.0179624.g004){ref-type="fig"}). The values in humans were 31% in the rostrum, 22% in the genu, 30% in the anterior midbody, 33% in the posterior midbody, 30% in the isthmus, and 33% in the splenium ([Fig 4B, 4C and 4E--4H](#pone.0179624.g004){ref-type="fig"}). Finally, areas of the CC subdivisions increased rapidly during infancy and continued to increase slowly during the juvenile stage in both species ([Fig 4C--4H](#pone.0179624.g004){ref-type="fig"}). The only exception was the rostrum of chimpanzees, which is detailed in in the Section "Differences between chimpanzees and humans". ### Differences between chimpanzees and humans {#sec028} There were four noticeable differences between the two species. First, at the beginning of infancy, the normalized rostral body area of humans was greater than that of other CC subdivisions, and, by the end of infancy, it had already reached 83% of that of the adult. This prominence of the rostral body was not seen in chimpanzees. In humans, the normalized rostral body area expands from 43% to 83% during infancy, while this expansion ranged from 26% to 60% in chimpanzees ([Fig 4D](#pone.0179624.g004){ref-type="fig"}). Second, although areas of the CC subdivisions increased rapidly during infancy in both species, the slope was steeper in humans than in chimpanzees. In chimpanzees, the normalized areas of the CC subdivisions expanded during infancy from 19 to 61% in the genu, from 26 to 60% in the rostral body, from 29 to 51% in the anterior midbody, from 27 to 48% in the posterior midbody, from 27 to 50% in the isthmus, and from 25 to 51% in the splenium ([Fig 4C--4H](#pone.0179624.g004){ref-type="fig"}). In humans, the corresponding values were: from 22% to 80% in the genu; from 43% to 83% in the rostral body; from 30% to 74% in the anterior midbody; from 33% to 69% in the posterior midbody; from 30% to 65% in the isthmus; and from 33% to 72% in the splenium ([Fig 4C--4H](#pone.0179624.g004){ref-type="fig"}). Third, the normalized areas and the CC subdivisions of humans were greater than that of chimpanzees, except for the rostrum, at the end of the juvenile stage. In chimpanzees, the normalized areas were: 75% in the genu; 73% in the rostral body; 64% in the anterior midbody; 67% in the posterior midbody; 68% in the isthmus; and 72% in the splenium at the end of juvenile stage ([Fig 4C--4H](#pone.0179624.g004){ref-type="fig"}). In humans, the corresponding values were: 85% in the genu; 89% in the rostral body; 84% in the anterior midbody; 81% in the posterior midbody; 82% in the isthmus; and 88% in the splenium ([Fig 4C--4H](#pone.0179624.g004){ref-type="fig"}). Finally, the area of the rostrum of the chimpanzees increased more rapidly during the juvenile stage than that of the humans, and the area at the end of the juvenile stage was close to that of adults. In chimpanzees, the normalized area of the rostrum increased from 64% to 94% during juvenile stage ([Fig 4B](#pone.0179624.g004){ref-type="fig"}), while, in humans, the increase was from 66% to 72% ([Fig 4B](#pone.0179624.g004){ref-type="fig"}). Discussion {#sec029} ========== General inter-species similarities and differences in the developmental trajectories {#sec030} ------------------------------------------------------------------------------------ The major finding in this study was the identification, in chimpanzees, of a rapid increase in the total CC and the subdivisions during infancy, followed by a gradual increase during the juvenile stage. This developmental trajectory was similar to that reported in humans, and the increase was attributed to the formation of myelin sheaths around the axons that pass through the CC \[[@pone.0179624.ref019], [@pone.0179624.ref020], [@pone.0179624.ref024], [@pone.0179624.ref037], [@pone.0179624.ref038], [@pone.0179624.ref041], [@pone.0179624.ref056]\]. Accordingly, diffusion tensor imaging studies of human brains have shown that the fractional anisotropy---a measure that reflects axonal alignment, density, and myelination---increases during development \[[@pone.0179624.ref037], [@pone.0179624.ref041], [@pone.0179624.ref057]--[@pone.0179624.ref060]\], with a reduction in radial diffusion \[[@pone.0179624.ref061]\], indicating that myelination is the major cause of the volume increase. The major differences between humans and chimpanzees were the slope of the developmental curve during infancy, which was steeper in humans than in chimpanzees, and the normalized CC areas during the juvenile stage, both of which were greater in humans than in chimpanzees (inter-species differences in the rostral body and the rostrum are discussed in the Sections "Development of the rostral body" and "Development of the rostrum"). These findings are congruent with a previous volumetric study, which indicated that cerebral volume and the substructures increased more rapidly in humans than in chimpanzees \[[@pone.0179624.ref050]\]. Since early infancy is critical for postnatal brain development in humans, in terms of volume increase \[[@pone.0179624.ref062], [@pone.0179624.ref063]\], synaptic elaboration, myelination \[[@pone.0179624.ref064]\], and the establishment of a default mode network \[[@pone.0179624.ref065]\], inter-species differences during this period might be related to the functional differences between humans and chimpanzees. Whether the emergence of the rapid increase during infancy is a marker of hominoids needs to be elucidated. Development of the rostral body {#sec031} ------------------------------- The development of the human rostral body was characterized by a greater normalized area than other CC subdivisions and a rapid increase during infancy than that of chimpanzees. This early maturation might indicate evolutional changes in brain anatomy and functions. The rostral body carries fibers between the medial prefrontal and premotor cortices \[[@pone.0179624.ref066]\]. These cortical regions play an important role in behavior planning and control, such as response preparation, selection, and response control \[[@pone.0179624.ref067]--[@pone.0179624.ref069]\]. A DTI study of pediatric human traumatic brain injury suggested that the degree of damage in the rostral body is related to verbal working memory and mathematical concepts. A reduction in the area was also related to attention deficit hyperactivity disorder \[[@pone.0179624.ref070]\]. Since the functions related to the rostral body, which can be summarized as "executive functions," are highly specialized in humans, one might argue that the early maturation seen in humans is related to cognitive and behavioral differences between humans and other hominoids. This concept must be further investigated. Development of the rostrum {#sec032} -------------------------- The development of the chimpanzee rostrum was characterized by a faster increase during the juvenile stage than that of humans. The size of the area at the end of the juvenile stage was close to that of an adult. This explained why the increase in the rostrum area was not observed in the previous study that targeted chimpanzees older than our study population \[[@pone.0179624.ref043]\]. A histological evaluation of the primate brain showed that the rostrum carries fibers between the orbitofrontal and dorsolateral prefrontal cortices \[[@pone.0179624.ref007]\]. These regions are important for different processes of attention: the orbitofrontal cortex controls emotional motivation behavior, and the dorsolateral prefrontal cortex monitors cognition to develop efficient control of interfering sensory stimuli \[[@pone.0179624.ref071]\]. Accordingly, the rostrum is involved in the development of attention and inhibitory control \[[@pone.0179624.ref072]--[@pone.0179624.ref074]\], and the transfer of information between prefrontal cortices \[[@pone.0179624.ref075]\]. In chimpanzees, inhibitory control of saccades was weaker than that of humans, which led to frequent saccades and short fixations of eye movement \[[@pone.0179624.ref076]--[@pone.0179624.ref078]\]. Taken together, the development of the rostrum in chimpanzees might be related to inter-species differences in attention and inhibitory control. The scientific environment in chimpanzee research and the use of legacy data {#sec033} ---------------------------------------------------------------------------- In the USA, the National Institutes of Health (NIH) has ceased all invasive biomedical studies on chimpanzees \[[@pone.0179624.ref079]--[@pone.0179624.ref081]\]. In 2013, the NIH had decided to retire more than 300 chimpanzees, leaving 50 chimpanzees for research in case of a public-health emergency. In 2015, the NIH made the decision that they would send this remaining population to sanctuaries in subsequent years. Thus, there was a push to repurpose legacy chimpanzee brain data. After the NIH decision in 2015, a biobank of chimpanzee brains, including MRI data, was developed through NIH funding for public use (<http://www.chimpanzeebrain.org/>). In Japan, our longitudinal MRI study of chimpanzee infants began in KUPRI in 2000 \[[@pone.0179624.ref049], [@pone.0179624.ref050]\], and terminated in 2012. Despite the relatively small sample size, which makes statistical analysis difficult, this longitudinally evaluated cohort is still precious and might contribute to the research community, since such a longitudinal dataset does not exist in the biobank in the USA, and it is difficult to collect new data for use now and in the future. Chimpanzees are among the endangered species and must be protected. Limitations {#sec034} ----------- There are several limitations to our study. First, one of the chimpanzees in the present study, Pico, died at the age of two years, and had complications from spinal cord compression with paraplegia. Although there was no noticeable abnormality on the brain MRI, the existence of a subtle abnormality was difficult to detect during routine radiological evaluation. Therefore, we also analyzed the developmental trajectories without Pico's data. We found that the results without Pico's data did not change our conclusion obtained from the full dataset ([S1](#pone.0179624.s001){ref-type="supplementary-material"} and [S2](#pone.0179624.s002){ref-type="supplementary-material"} Figs; [S3 Table](#pone.0179624.s005){ref-type="supplementary-material"}; [S1 File](#pone.0179624.s006){ref-type="supplementary-material"}). Second, in our study, the adult chimpanzees (used as references to normalize areas of the CC and the subdivisions) were scanned using two different protocols (SPGR or FGRE-IrP). To investigate the effect of scan protocol on image quantification, we compared the midsagittal CC area in a brain sample from an adult chimpanzee, scanned with SPGR and FGRE-IrP ([S2 File](#pone.0179624.s007){ref-type="supplementary-material"}). We found that the CC area, as measured by the two MRI sequences, are indeed close (0.2% difference) and comparable to the intra-rater difference for the manual delineation (1.7%). Therefore, we assumed that the difference in the scan protocol had little effect on the quantification of the CC area ([S2 File](#pone.0179624.s007){ref-type="supplementary-material"}). Since chimpanzee brain MRIs available for research purposes are limited, it is common to combine MRIs scanned with different scanners and acquisition sequences \[[@pone.0179624.ref043]\]. We recognize that the issue related to the heterogeneity of MRIs is one of the limitations generally seen in the field of chimpanzee neuroimaging studies. Third, the prenatal period was not included in the present study. The inclusion of prenatal development is important since neuronal maturation at birth varies across species \[[@pone.0179624.ref082]\]. One possibility to enable the evaluation of prenatal development is to utilize longitudinally-acquired, legacy sonography data \[[@pone.0179624.ref051]\], which might make for an interesting future study. Fourth, we defined developmental stages based on physical milestones, such as dental eruption, weight increase, and sexual maturation for the interspecies comparison, since this anthropological definition is a valid approach by which to compare the development among different primates \[[@pone.0179624.ref049], [@pone.0179624.ref050], [@pone.0179624.ref083]\]. However, the relationship between physical and neuronal development is not fully understood. The appropriateness of developmental staging based on neuronal milestones has yet to be investigated. Finally, the method used to draw the boundaries of the seven CC subdivisions on T1-weighted MRI was based on the studies about the topographical organization of the white matter fibers of the adult human brain. The applicability of the MRI-based anatomical definition throughout different developmental stages has not been fully validated. Cross-species longitudinal evaluation of the topological organization of CC fibers during development is essential for validation. In summary, our results suggest that CC development in chimpanzees and humans is characterized by a rapid increase during infancy, followed by a relatively slow increase during the juvenile stage. The differences between the two species include a tendency toward a greater increase in the human CC areas, especially in the rostral body, during infancy, compared to that observed in chimpanzees. A tendency toward a greater increase in the rostrum during the juvenile stage in chimpanzees, compared to that observed in humans, was also observed. The interspecies differences in the developmental trajectories of the rostral body and the rostrum might underpin evolutional changes in the executive functions related to these areas. Supporting information {#sec035} ====================== ###### Evaluation of the rostrum and genu during development in young chimpanzee data with and without Pico's data. Age-related changes in the rostrum and genu during infancy and the juvenile stage (6 to 72 months) are shown for chimpanzees with and without Pico's data (n = 4; n = 3). (A) rostrum, (B) genu. The bar below the graphs indicates the developmental stage. The indicated developmental stages are infancy (open bar) and the juvenile stage (hatched bar). (PDF) ###### Click here for additional data file. ###### Evaluation of the normalized rostrum and genu during development in chimpanzee data with and without Pico's data. Age-related changes in the rostrum and genu, relative to the adult areas, during infancy and the juvenile stage (6 to 72 months) are shown for chimpanzees with and without Pico's data (n = 4; n = 3). (A) rostrum, (B) genu. The bar below the graphs indicates the developmental stage. The indicated developmental stages are infancy (open bar) and the juvenile stage (hatched bar). (PDF) ###### Click here for additional data file. ###### Age, total CC, and CC subdivisions in chimpanzees and humans during the developmental course of the study period. (PDF) ###### Click here for additional data file. ###### Results of the linear regression model of age-related changes in the corpus callosum areas during the adult stage. Age-related changes in the total CC and the CC subdivisions during the adult stage (n = 10; mean (s.d.) age, 31.2 (5.8) years). F = F value, R^2^ = adjusted R^2^ value. "F," "R^2^," and "sig" indicate the results of the statistical analysis for the age-related changes in the total CC and the CC subdivisions with a linear regression model. "n.s." indicates "not significant." (DOCX) ###### Click here for additional data file. ###### Results of polynomial regression modeling of the developmental trajectories of the rostrum and genu in chimpanzees with and without Pico's data. Age-related changes in the rostrum and genu in chimpanzees with and without Pico's data (n = 4; n = 3). F = F value, R^2^ = adjusted R^2^ value. "Best fitting model," "F" "R^2^," and "sig" indicate the results of the statistical analysis for the age-related changes in the rostrum and genu with a polynomial regression model. The best-fitting model represents the best-fitting model of the linear, quadratic, and cubic regression models. (DOCX) ###### Click here for additional data file. ###### Comparison of the developmental trajectories of the rostrum and genu in young chimpanzees with and without Pico's data. (DOCX) ###### Click here for additional data file. ###### Comparison of the measurements of the chimpanzee CC area acquired with different MRI sequences. (DOCX) ###### Click here for additional data file. We thank T. Nishimura, A. Watanabe, A. Kaneko, S. Goto, S. Watanabe, K. Kumazaki, N. Maeda, M. Tanaka, M. Hayashi, T. Imura, and K. Matsubayashi for assisting with the care of chimpanzees during scanning. We also thank the personnel at the Centre for Human Evolution Modelling Research at KUPRI for daily care of the chimpanzees. We also thank S. Mori for helpful comments, and M. McAllister for help with manuscript editing. We would like to acknowledge partial support for the statistical analysis from the National Center for Research Resources and the National Center for Advancing Translational Sciences (NCATS) of the National Institutes of Health, and the statistician of the Johns Hopkins Biostatistics Center, A. Sanyal and C. Thompson. [^1]: Competing Interests:The authors have declared that no competing interests exist. [^2]: Conceptualization: TS.Data curation: TS MM.Formal analysis: TS KO.Funding acquisition: TS MM.Investigation: TS AM JS TM-N YH MT TM.Methodology: TS AM YH KO.Project administration: TS AM TM HO.Resources: TS AM JS MM TM-N YH MT TM.Software: TS.Validation: TS KO.Visualization: TS.Writing -- original draft: TS KO.Writing -- review & editing: TS AM JS TM-N YH HO KO.	3.09375	3	[ 0.0031280517578125, -0.0029754638671875, 0.012451171875, 0.00189208984375, 0.009033203125, 0.009033203125, 0.0169677734375, 0.00299072265625, 0.0079345703125, -0.02392578125, -0.01458740234375, -0.00019168853759765625, 0.0048828125, -0.004150390625, 0.00144195556640625, 0.001953125, 0.006256103515625, -0.012451171875, 0.0118408203125, -0.0186767578125, -0.0218505859375, 0.015625, -0.004852294921875, -0.015380859375, -0.0023193359375, -0.0250244140625, 0.01025390625, 0.01397705078125, -0.011962890625, -0.006744384765625, 0.01153564453125, 0.00177764892578125, 0.0103759765625, 0.00439453125, -0.0029449462890625, 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Photo Obese children who cut back on their sugar intake see improvements in their blood pressure, cholesterol readings and other markers of health after just 10 days, a rigorous new study found. The new research may help shed light on a question scientists have long debated: Is sugar itself harming health, or is the weight gain that comes from consuming sugary drinks and foods mainly what contributes to illness over the long term? In the new study, which was financed by the National Institutes of Health and published Tuesday in the journal Obesity, scientists designed a clinical experiment to attempt to answer this question. They removed foods with added sugar from a group of children’s diets and replaced them with other types of carbohydrates so that the subjects’ weight and overall calorie intake remained roughly the same. After 10 days, the children showed dramatic improvements, despite losing little or no weight. The findings add to the argument that all calories are not created equal, and they suggest that those from sugar are especially likely to contribute to Type 2 diabetes and other metabolic diseases, which are on the rise in children, said the study’s lead author, Dr. Robert Lustig, a pediatric endocrinologist at the Benioff Children’s Hospital of the University of California, San Francisco. “This paper says we can turn a child’s metabolic health around in 10 days without changing calories and without changing weight – just by taking the added sugars out of their diet,” he said. “From a clinical standpoint, from a health care standpoint, that’s very important.” Added sugars — the extra sweeteners food companies put in their products, not the sugar that occurs naturally in foods like fruit – are a topic of growing debate. In February, the federal government’s Dietary Guidelines Advisory Committee recommended that Americans limit their intake of added sugars to no more than 10 percent of daily calories. In 2014, the Food and Drug Administration proposed that food companies include a line on their nutrition labels listing the amount of added sugars in their products. After the dietary guidelines committee issued its report earlier this year, the agency expanded on its 2014 proposal, saying that companies should also list a “daily percent value” for added sugars on their labels in line with the 10 percent recommendation. The proposed changes have been strongly opposed by the food industry as unscientific. The Sugar Association, a trade group, said the F.D.A. was “making assertions that lack adequate scientific evidence,” and the Grocery Manufacturers Association criticized the standards the agency used to establish the daily value as being “inadequate.” The newly released study is timely in part because it lowered sugar intake among children to roughly 10 percent of daily calories, the amount recommended by the dietary guidelines committee. For their study, the scientists recruited 43 children between the ages of 9 and 18 who were considered at particularly high risk of diabetes and related disorders. All the subjects were black or Hispanic and obese, and had at least one or more symptoms of metabolic syndrome, a cluster of risk factors that includes hypertension, high blood sugar, abnormal cholesterol and excess body fat around the waist. On average, the subjects had been getting about 27 percent of their daily calories from sugar. By comparison, the average American takes in about 15 percent, though children typically consume much more than this in part because they have the highest intake of sugar-sweetened beverages. The study authors paired the subjects with dietitians. They then replaced the sugary foods in their diets with other foods purchased from local grocery stores. The goal was not to eliminate carbohydrates, but to reduce sugary foods and replace them with starchy foods without lowering body weight or calorie intake. “Wherever there was food with added sugar in their diets, we took it out and we replaced it with a no-added-sugar version,” Dr. Lustig said. So instead of yogurt sweetened with sugar, the children ate bagels. Instead of pastries, they were given baked potato chips. Instead of chicken teriyaki – which typically contains a lot of sugar – they ate turkey hot dogs or burgers for lunch. The remaining sugar in their diet came mostly from fresh fruit. Because the scientists were working on a tight N.I.H. budget, they could only carry out the costly intervention for nine days. But in that short space of time, they saw marked changes. On average, the subjects’ LDL cholesterol, the kind implicated in heart disease, fell by 10 points. Their diastolic blood pressure fell five points. Their triglycerides, a type of fat that travels in the blood and contributes to heart disease, dropped 33 points. And their fasting blood sugar and insulin levels – indicators of their diabetes risk – likewise markedly improved. One expert who was not involved in the new research, Dr. Frank Hu of the Harvard T.H. Chan School of Public Health, said that the study “strengthens the existing evidence on the relationship between added sugar intake and metabolic disease.” “This kind of study is very difficult to do,” he said. “But it provides a proof of concept that in a high risk population, reducing consumption of added sugar can have multiple metabolic benefits.” Dr. Sonia Caprio, a pediatric endocrinologist and professor of pediatrics at Yale Medical School, said that although the study was small, “it addressed the issue in an original way and tried to isolate the effect of sugar on metabolic syndrome and insulin resistance.” “This is an important area of research that might solve some of the metabolic issues that we are facing in children, particularly in adolescents,” she said. “This study needs to be taken seriously, and we need to expand on it.” Related: For more fitness, food and wellness news, “like” our Facebook page. 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Introduction {#Sec1} ============ When humans spread throughout the Earth, high-altitude environments presented a significant challenge to the people living within them. Low air pressure, hypoxia, strong solar radiation and low temperature exert great pressure on the survival of local people. Genetic factors in both the nuclear genome and mitochondrial DNA (mtDNA) genome play great roles in the adaptation to high-altitude environments, which was considered as natural impacts on human evolution and adaptation^[@CR1]^. In the past few years, an increasing number of genetic studies on the nuclear genome have shown that a series of genes have been involved in high-altitude adaptation in Tibetans^[@CR2]--[@CR8]^, Andeans^[@CR8],[@CR9]^ and Ethiopians^[@CR10],[@CR11]^, and these genes are mainly distributed in the hypoxia-inducible factor signaling pathway and the TP53 pathway. However, the role of the mtDNA genome in high-altitude adaptation are still in discussion and should receive more attention. Mitochondria are known as the cell's power plant, where cellular fuel is oxidized to provide energy for metabolism. Mitochondrial function is dependent on mtDNA, and mtDNA is well established as a genetic marker. A high mutation rate, small genome size, maternal inheritance, and lack of recombination make mtDNA an important tool for studying genetic structure in different populations. Besides, analyses of mtDNA sequences provide clues for exploring the genetic relationships between different populations, which contributes to deep understanding the role of mtDNA variations in human evolution. In addition to 2 rRNAs and 22 tRNAs, mtDNA encodes 13 core subunits related to oxidative phosphorylation (OXPHOS). Approximately 90% of the energy required by the cell is provided by OXPHOS, which is significantly affected by mtDNA variations. Hence, it is commonly believed that mtDNA contributed to high-altitude adaptation in high-altitude natives^[@CR12],[@CR13]^. There are three groups of high-altitude natives living in China, including high-altitude Tajiks (hereafter referred to as HA-Tajiks), Tibetans and Sherpas. The HA-Tajik population is one of 56 ethnic groups in China. HA-Tajiks have lived for generations in the Xinjiang Taxkorgan Tajik Autonomous County, where the average elevation is more than 4,000 m. Taxkorgan is perched in the highest part of the Pamirs. The world's second highest peak, Mount Qogir, towers over the south, and in the north stands Mount Muztagata, "the father of ice peaks." The HA-Tajik people seldom intermarry with other ethnic groups, and this ethnic identity means that their genetic structure shows little mixing with outsiders. Thus, it is attractive and feasible to explore the role of mtDNA in the high-altitude adaptation of HA-Tajiks. Tibetans are considered to be an ethnic group that is adapted to the high-altitude environment, and it has been reported that mtDNA variations influence the efficiency of oxygen utilization and function in native Tibetans^[@CR14]^. Sherpas live south of the Himalayas and are famous for their physical ability in climbing Mount Everest and are well-known as porters in the Himalayas. Their characteristics at high altitudes are considered as markers of high-altitude adaptation. Previous studies have found that eNOS, PPARA^[@CR15]^, HIF, ACE^[@CR16]^ and EPAS1 in the nuclear genome and CYTB, ATP6, ND1, ND4 and ND5 in the mtDNA genome play a great role in the high-altitude adaptation of Sherpas^[@CR17]^. Recently, a study analyzed mtDNA genomes in different populations in Central Asia located around the Pamirs^[@CR18]^, and different populations of Tajiks living at high altitude were also investigated. Because partial mtDNA sequences are not able to provide enough information, so complete mtDNA genome sequences were required for this research. To better understand the genetic structure of the mtDNA genome and identify the possible role of the mtDNA genome in high-altitude adaptation in HA-Tajiks, 80 HA-Tajik individuals living in Taxkorgan were enrolled, and their whole mtDNA genomes were sequenced. We also examined the mtDNA genomes of Tibetans and Sherpas as well as other reported Tajik populations^[@CR18]^ to compare the genetic differences between them and to analyze different patterns of high-altitude adaptation between three high-altitude native populations at the Qinghai-Tibetan Plateau and in the Pamirs from perspectives of mtDNA variations. Results {#Sec2} ======= Study population and reference population in this study {#Sec3} ------------------------------------------------------- A total of 11 populations, including 706 subjects, were analyzed in this study. The basic information of the subjects is listed in Table [1](#Tab1){ref-type="table"}.Table 1Basic information of the populations enrolled in this study.PopulationCategorySizeLocationSourceHigh-altitude TajikHighlander80Taxkorgan, Xinjiang, ChinaThis studySarikoli TajikHighlander86Taxkorgan, Xinjiang, ChinaReferenceWakhi TajikHighlander66Taxkorgan, Xinjiang, ChinaReferencePamirs TajikHighlander50Gorno-Badakhshan, TajikistanReferenceLowland TajikLowlander28Dushanbe, TajikistanReferenceEast Pamir KyrgyzHighlander68Taxkorgan, Xinjiang, ChinaReferenceLowland KyrgyzLowlander54Artux, Xinjiang, ChinaReferenceLowland UygurLowlander27Artux, Xinjiang, ChinaReferenceSherpaHighlander76Tibet, ChinaReferenceBeijing Han ChineseLowlander103Beijing, China1000 Genomes ProjectTibetanHighlander68Tibet, ChinaReference mtDNA genetic diversity of Tajiks {#Sec4} --------------------------------- The number of haplotypes, nucleotide diversity, haplotype diversity, Tajima's D and Fu's Fs were 73, 0.00216 ± 0.00024, 0.997 ± 0.00001, − 2.277 and − 33.741, respectively. The main frequencies of the haplogroups in the 80 HA-Tajiks analyzed in this study are shown in Fig. [1](#Fig1){ref-type="fig"}, and the major haplogroups were U, followed by H, T and J, indicating that the HA-Tajik population settled in Taxkorgan, China, may have originated from Europe^[@CR18],[@CR19]^. Haplogroup of each subject was provided in Table [S1](#MOESM1){ref-type="media"}. Phylogeny of 80 HA-Tajiks calculated by mtPhyl (version 5.003) was provided as dataset1 with a xlsx file. Detailed frequencies of haplogroups in 80 HA-Tajiks as well as other reference population were provided in Table [S2](#MOESM2){ref-type="media"}.Figure 1The haplogroup profiles of HA-Tajiks enrolled in this study. Major haplogroups were U, followed by H, T and J. Haplogroups were merged for brevity. Detailed frequencies of haplogroups in HA-Tajiks were listed in Table [S2](#MOESM2){ref-type="media"}. Bayesian skyline plot (BSP) for HA-Tajiks {#Sec5} ----------------------------------------- BSP was conducted to trace historical variations in population size based on coding regions of mtDNA genome (Fig. [2](#Fig2){ref-type="fig"}). Although the sample size of HA-Tajiks is small in this study, it could be inferred that the effective population size of HA-Tajiks is steadily growing, which is consistent with demographic data of HA-Tajiks in China, especially in recent years (<https://www.china.org.cn/e-groups/shaoshu/shao-2-tajik.htm>). Besides, the expansion of HA-Tajiks revealed by the BSP is also in accordance with the negative Tajima's D and Fu's Fs.Figure 2Bayesian Skyline Plot of HA-Tajik population history. BSP obtained by BEAST showed population history predicted from mitochondrial coding regions of 80 HA-Tajik subjects. The black line in the middle indicates the median population size predict from Bayesian posterior distribution. The population expansion may start from 10--15 kya before present. Genetic relationship of HA-Tajiks with other populations {#Sec6} -------------------------------------------------------- PCA was applied based on the frequencies of haplogroups in the mtDNA genomes to represent the relationships among the 11 populations enrolled in this study after transformation (Fig. [3](#Fig3){ref-type="fig"}). The detailed frequencies of the mtDNA haplogroups in the 11 populations are provided in Table [S2](#MOESM2){ref-type="media"}. Further analysis based on ARLEQUIN 3.5.1.3 and MEGA 7.0 also showed that the HA-Tajiks enrolled in this study presented a close genetic relationship with the Wakhi Tajiks, Pamiri Tajiks and Sarikoli Tajiks (Figs. [3](#Fig3){ref-type="fig"}, [4](#Fig4){ref-type="fig"}), indicating that they may belong to one nation, with differences in their geographical distributions. Moreover, Figs. [3](#Fig3){ref-type="fig"} and [4](#Fig4){ref-type="fig"} indicate that the genetic relationships of HA-Tajiks with Tibetans and Sherpas are distant, while Tibetans and Sherpas show a close relationship. Hence, it could be inferred that HA-Tajiks may exhibit a different pattern of high-altitude adaptation compared to Tibetans and Sherpas from the perspective of the mtDNA genome. To further explore these differences, a detailed comparison of different regions in the mtDNA genome between HA-Tajiks and Tibetans as well as Sherpas was performed in subsequent analysis.Figure 3PCA of populations from HA-Tajiks and other ten populations. PC map of populations based on mtDNA haplogroup frequencies (Table [S2](#MOESM2){ref-type="media"}). Figure 4Genetic distance of populations from HA-Tajiks and other ten populations based on mtDNA haplogroup frequencies. Different variations in the mtDNA genome between Tajiks, Tibetans and Sherpas {#Sec7} ----------------------------------------------------------------------------- After comparison to the rCRS, the number of variations in each polymorphism of the mtDNA genome was calculated in HA-Tajiks, Tibetans and Sherpas. Taking polymorphism 10400T of the mtDNA genome as an example, the numbers of variants were determined to be 6, 53 and 49, so the numbers of non-variants were 74, 15 and 27 in HA-Tajiks, Tibetans and Sherpas, respectively. At the statistical significance level of 0.025, our results indicated that there were significant differences in the distribution of many polymorphisms in the mtDNA genomes. As a result, only p values below 0.0000001 and polymorphisms in 13 genes belonging to the OXPHOS pathway encoded by the mtDNA genome are presented. The comparisons between HA-Tajiks and Tibetans and between HA-Tajiks and Sherpas are listed in Tables [2](#Tab2){ref-type="table"} and [3](#Tab3){ref-type="table"}, and the remaining results related to OXPHOS are provided in Table [S3](#MOESM3){ref-type="media"} and Table [S4](#MOESM4){ref-type="media"}.Table 2Results with p values below 0.0000001 in the comparison of the mtDNA genome between Tibetans and HA-Tajiks.PolymorphismsAmino acid changeRegionsTibetanHA-Tajiksχ^2^p valuesVariantNon-variantVariantNon-variant10400 TNoND3531567476.08\< 0.000000114783CNoCYTB531567476.08\< 0.000000115043ANoCYTB531577373.00\< 0.000000115301ANoCYTB531567476.08\< 0.0000001 Table 3Results with p values below 0.0000001 in the comparison of the mtDNA genome between Sherpas and HA-Tajiks.PolymorphismsAmino acid changeRegionsSherpaHA-Tajiksχ^2^p valuesvariantnon-variantvariantnon-variant3594TNoND1076404051.10\< 0.00000014104GNoND1076404051.10\< 0.00000014769GNoND2760423847.73\< 0.00000017028TNoCOX1751433742.71\< 0.00000017146GYesCOX1076404051.10\< 0.00000017256TNoCOX1373404041.40\< 0.00000018468TNoATP8076404051.10\< 0.00000018655TNoATP6076404051.10\< 0.00000018860GYesATP6760404051.10\< 0.000000110400TNoND3492767455.42\< 0.000000110664TNoND4L076404051.10\< 0.000000110688ANoND4L076404051.10\< 0.000000110810CNoND4076404051.10\< 0.000000110915CNoND4076404051.10\< 0.000000111719ANoND4751433742.71\< 0.000000113105GYesND5076404051.10\< 0.000000113276GYesND5076404051.10\< 0.000000113506TNoND5076404051.10\< 0.000000113650TNoND5076404051.10\< 0.000000114766TYesCYTB751433742.71\< 0.000000114783CNoCYTB492767455.42\< 0.000000115043ANoCYTB492777352.59\< 0.000000115301ANoCYTB492767455.42\< 0.000000115326GYesCYTB760404051.10\< 0.0000001 Table [2](#Tab2){ref-type="table"} showed that the frequencies of the variant polymorphisms 10400T, 14783C, 15043A and 15301A in Tibetans were significantly higher than those in Tajiks. Polymorphism 10400T belongs to ND3 and polymorphisms 14783C, 15043A and 15301A to CYTB. Hence, it seemed that polymorphisms in CYTB may provide more clues about high-altitude adaptation in Tibetans on the Qinghai-Tibetan Plateau than in HA-Tajiks in the Pamirs, and other regions of the mtDNA genome should be evaluated in relation to high-altitude adaptation in HA-Tajiks. Compared to Sherpas, HA-Tajiks exhibited more polymorphisms in multiple regions of the mtDNA genome, and detailed results are listed in Table [3](#Tab3){ref-type="table"}. The mtDNA genome of HA-Tajiks showed significant differences in ND1, ND2, COX1, ATP8, ATP6, ND3, ND4L, ND4, ND5 and CYTB, which are more complicated than the comparisons between Tajiks and Tibetans. Polymorphisms 14783C and 15301A of CYTB showed the most significant differences in the distribution between HA-Tajiks and Sherpas. In addition, it could also be inferred that Tibetans and Sherpas may present different patterns of high-altitude adaptation from the perspective of the mtDNA genome, because frequencies of certain variants in mtDNA genome also showed significant differences between Tibetans and Sherpas. Discussion {#Sec8} ========== This is the first study to compare and analyze molecular evidence of high-altitude adaptation in three high-altitude native groups from the perspective of the mitochondrial genome. In this study, the whole mtDNA genomes of 80 HA-Tajiks living in the Pamirs were sequenced, and the major mitochondrial haplogroups in HA-Tajiks were U, H and T as well as J confirmed that HA-Tajiks settled in the Pamirs were likely to be originated in Europe. BSP revealed by BEAST indicated that the effective population size was steadily increasing, which was in consistent with the current status of HA-Tajiks in China. Based on PCA and genetic distance analysis, we found that the HA-Tajiks enrolled in this study exhibited a close relationship with Wakhi Tajiks, Pamiri Tajiks and Sarikoli Tajiks. The difference in the mtDNA genome between HA-Tajiks and Sherpas was significantly greater than the differences between HA-Tajiks and Tibetans, suggesting different patterns of high-altitude adaptation were existed between HA-Tajiks, Tibetans and Sherpas. BSP was an effective tool to analyze population size based on mtDNA genome sequences. However, different settings of analysis methods would generate various results even dealing with the same sequences. Compared to Peng's research^[@CR18]^, significant decline in effective population size was observed by BSPs, which is conflict with negative Tajima's D and Fu's Fs yielded in his research. Possible explanations were different sample strategies, and mainly were attributed to different parameters of strict clock model and analysis methods. In Peng's research, this strict clock model was 1.404 × 10^−8^ substitutions per site per year and the TrN + I + G substitution model, and 2.308 × 10^−8^ substitutions per site per year as well as the GTR model of nucleotide substitution with empirical base frequencies were employed in this research. In addition, appropriate analytical methods are not easily determined when facing big data. Hence, parameters setting of software are not only depend on references but also in accordance to the actual situation as well as population history. Although HA-Tajiks, Tibetans and Sherpas are high-altitude natives, they exhibited great differences in their languages, customs and origins^[@CR18],[@CR20]^. Even after the long-term settlement of high-altitude environments, these three groups may show different responses to hypoxia stimulation at the molecular level, and variants in the mtDNA genome provided an useful tool for further analysis^[@CR1]^. Mitochondrion have been reported to be involved in high-altitude adaptation in Tibetans and Sherpas. The mitochondrial nt3010G-nt3970C haplotype^[@CR21]^ and haplogroup M9a1a1c1b in Tibetans^[@CR13],[@CR22]^ and haplogroups C4a3b1 and A4e3a in Sherpas^[@CR17]^ contributed to high-altitude adaptation. Compared to Tibetans, the distribution of polymorphisms 10400T, 14783C, 15043A and 15301A showed the most significant differences in Tajiks. However, the frequencies of these polymorphisms in Tajiks were significantly lower than those in Tibetans, indicating that other regions of the mtDNA genome should be considered in the assessment of the role of mtDNA in high-altitude adaptation in HA-Tajiks. Among the 13 genes belonging to the OXPHOS pathway, we found that the frequency of variant polymorphism 12372 (12372A) in ND5 was the most significantly increased compared to that in Tibetans (Table [S3](#MOESM3){ref-type="media"}). Taking U haplogroup as an example, 12372A is the marker of the U haplogroup, which accounted for the main lineage in the 80 HA-Tajiks enrolled in this study. Functional changes in 12372A were not detected, and this polymorphism showed no association with sudden infant death syndrome in the Swiss population^[@CR23]^. Although the 12372A variant in ND5 does not result in an amino acid change, it may affect the DNA-RNA network, mRNA stability, RNA splicing, translation kinetics and protein folding, etc.^[@CR15],[@CR24]^, which ultimately contributes to disease progression. It seems that many pathogenic mutations are enriched in the mtDNA genomes of high-altitude native peoples^[@CR13]^. However, these deleterious mutations do not induce a harmful phenotype in high-altitude natives, indicating that the diseases caused by mitochondrial mutations may be population specific. Hence, the role of 12372A in high-altitude adaptation in Tajiks needs to be reevaluated with larger samples, and the molecular mechanism associated with the 12372A mutation should be analyzed in further studies. In the comparison between Tajiks and Sherpas, the frequencies of polymorphisms 3594T and 4104G in ND1, 7146G and 7256T in COX1, 8468T in ATP8, 8655T in ATP6, 10664T and 10688A in ND4L, 10810C and 10915C in ND4, and 13105G, 13276G, 13506T and 13650T in ND5 were found to be significantly higher in Tajiks. In addition, these variants seemed to be in linkage disequilibrium. Except for polymorphisms 7146G, 13105G and 13276G, all other polymorphisms mentioned above did not induce amino acid changes. 7146G, 13105G and 13276G result in amino acid changes from threonine to alanine, isoleucine to valine and methionine to valine, respectively. However, genotype--phenotype association and functional analyses based on three nonsynonymous amino acid mutations have seldom been reported. The 7146G mutation was located in COX1, and this variant may influence the biogenesis of COX1 and ultimately cause a different response at the molecular level in Tajiks in the Pamirs compared with Sherpas on the Qinghai-Tibetan plateau, which needs to be checked through functional analysis. 13105G and 13276G in ND5 were found to be associated with a risk of cervical cancer^[@CR25]^. ND5 is a primary subunit of nicotinamide adenine dinucleotides, and a mutation in ND5 can induce higher levels of reactive oxygen species^[@CR26]^. Combined with 13506T and 13650T in ND5, it seemed that alterations in ND5 would induce cumulative effects and may play a great role in high-altitude adaptation in Tajiks. However, the functional significance and the underlying mechanisms are unknown. Further investigations including molecular and biochemical studies are needed to explore the role of mutations in ND5 in high-altitude adaptation in HA-Tajiks. With the development of DNA sequencing technologies, next-generation sequencing has been widely applied in genetic studies, and the accuracy has increased significantly. Traditional Sanger sequencing based on PCR products was performed in this study, and we found that checking DNA sequencing results and the assembly of DNA fragments manually is highly time and energy consuming. Hence, in the acquisition of whole mtDNA genomes, next-generation sequencing should be considered as the main tool in further analysis, and Sanger sequencing could be a powerful additional complement, especially when the results acquired by next-generation sequencing are ambiguous. Conclusion {#Sec9} ========== We found that the lineages including U, H, T and J accounted for most HA-Tajik samples, indicating an European origin, and the HA-Tajik population showed a closer relationship with Wakhi Tajiks. BSP revealed by BEAST indicated that the effective population size was steadily increasing. Among 13 genes belonging to the OXPHOS pathway encoded by the mtDNA genome, HA-Tajiks showed the most significant differences in ND3 and CYTB compared to Tibetans. Compared to Sherpas, HA-Tajiks showed the most significant differences in ND1, ND2, COX1, ATP8, ATP6, ND3, ND4L, ND4, ND5 and CYTB. The associated biochemical changes and molecular mechanisms should be explored by functional investigations in further studies. Materials and methods {#Sec10} ===================== Ethics statements {#Sec11} ----------------- This research was approved by the ethics committee of the Third Military Medical University and the 950th Hospital of the PLA of China. All experiments were performed in accordance with relevant guidelines and regulations. All participants provided written informed consent before this investigation commenced. Study population {#Sec12} ---------------- A total of 80 unrelated HA-Tajiks (19 males, 52.9 ± 14.9 years, 19--76 years old; 61 females, 46.0 ± 15.0 years, 25--83 years old) were enrolled in this study. All subjects confirmed that they and their parents had been born and lived in Taxkorgan their whole lives in a questionnaire. Genomic DNA was extracted from venous blood using a DNA isolation kit (Omega Bio-Tek, Inc., Norcross, GA, USA) and was stored at − 20 °C for further use. mtDNA genome amplification and sequencing {#Sec13} ----------------------------------------- Eight pairs of primers were applied to amplify the mtDNA genome by polymerase chain reaction (PCR), and 22 primers were used for sequencing the PCR products^[@CR26]^ by Sanger dideoxy sequencing (detailed information of PCR amplification and sequencing primers is listed in Table [S5](#MOESM5){ref-type="media"} and [S6](#MOESM6){ref-type="media"}). The sequence of every PCR product was carefully checked according to the revised Cambridge Reference Sequence (rCRS) (GenBank: NC_012920). All of the sequences of the PCR products from each subject were integrated, and overlapping sequences were removed. After manual check of sequence diagrams, we found that the sequencing accuracy of 315--598 in sample 106, 120, 122, 133, 148, 149, 156, 167, 304, 320, and 16190--16396 in sample 119, 138, 225 were not satisfactory because of poly C structure existed. To make our work more convincing, we delete the mtDNA sequences in 315--598 and 16190--16396 belonging to D-loop region in samples mentioned above respectively, and these sequences were replaced as sequencing gaps. Finally, we obtained the mitochondrial genome sequence of 80 HA-Tajiks without 315--598 or 16189--16396 belonging to D-loop region for the following analysis. mtDNA haplogroup analysis and reference mtDNA genomes {#Sec14} ----------------------------------------------------- Each mtDNA genome of 80 HA-Tajik individuals was compared to Phylotree 17 rCRS to confirm variant sites and haplogroup by using Mitotool (<https://mitotool.kiz.ac.cn/)>^[@CR27]^ Ten additional populations living in East Asia and Central Asia, including Tibetans and Sherpas, were selected as references. The GenBank identification numbers of the Tibetans and Sherpas are provided as supplementary materials in Table [S7](#MOESM7){ref-type="media"}. Sequence data for the mtDNA genome were acquired from the 1000 Genomes Project or downloaded from GenBank as the references indicate. Variant sites and haplogroups were also acquired by using Mitotool as mentioned above. All the mtDNA sequences of 80 HA-Tajiks as mentioned above were deposited in Genbank (MT554196-MT554275). Analysis of mtDNA genomes {#Sec15} ------------------------- The mtDNA genetic diversity of HA-Tajiks (including haplotype numbers, nucleotide and haplotype diversity, Tajima's D, and Fu's Fs) was calculated by DnaSP6.0^[@CR28]^. The genetic distances between the HA-Tajiks and the reference populations based on the mtDNA genomes were analyzed by PCA based on the haplogroup distributions in different populations after normalized transformation^[@CR29]^. The Fst values between the populations enrolled in this study were calculated with ARLEQUIN 3.5.1.3^[@CR30]^. A phylogenetic tree was constructed with a neighbor-joining tree with MEGA 7.0. The phylogeny was constructed by using mtPhyl^[@CR31]^ (<https://sites.google.com/site/mtphyl/home>) with 80 complete mtDNA sequences in HA-Tajiks. The variants located in regions 16519, 16180--16193 and 310--315 and the AC indels in regions 515--522 were not included in the subsequent analysis^[@CR18]^. Bayesian phylogenetic analysis of HA-Tajiks {#Sec16} ------------------------------------------- The Bayesian skyline plots (BSPs) for HA-Tajiks were performed by BEAST v1.7.5. mtDNA coding region (np 577--16024) of each HA-Tajik subject was acquired by comparison of rCRS. After alignment of 80 mitochondrial coding region sequences, we employed the GTR model of nucleotide substitution with empirical base frequencies, and selected a strict clock model with the rate of 2.038 × 10^--8^ subs/site/year^[@CR32]^. Markov chain Monte Carlo (MVMV) was applied to estimate coalescent history. Parameters of MVMV were set as running for 400,000,000 generations and calculated every 4,000 generations. Results yielded by BEAST were visualized by Tracer 1.5 (<https://tree.bio.ed.ac.uk/software/tracer/>). Detailed differences in the mtDNA genomes between Tajiks, Tibetans and Sherpas {#Sec17} ------------------------------------------------------------------------------ To further identify the differences between HA-Tajiks, Tibetans and Sherpas, their whole-mtDNA-genome sequences were compared to the rCRS to confirm the variants in the mtDNA genomes in detail. The number of variants in different regions of the mtDNA genome was calculated by direct counting, and the variant distributions in different regions were analyzed by the chi-square test, which may reveal different patterns of high-altitude adaptation among HA-Tajiks, Tibetans and Sherpas. For the chi-square test, a Bonferroni correction was applied for multiple tests. Because the number of comparisons was 2 (HA-Tajik vs Tibetan, HA-Tajik vs Sherpa), the statistical significance level was set at 0.05/2 (0.025), and all p values were two-tailed. Supplementary information ========================= {#Sec18} Supplementary Table 1. Supplementary Table 2. Supplementary Table 3. Supplementary Table 4. Supplementary Table 5. Supplementary Table 6. Supplementary Table 7. Supplementary information. Publisher\'s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Supplementary information ========================= is available for this paper at 10.1038/s41598-020-67519-z. This work was supported by the second Tibetan Plateau Scientific Expedition and Research Program (STEP), Grant No. 2019QZKK0607, Key Project of the Logistics Research Program, PLA (BLJ18J005) and the National Natural Science Foundation of China (81571843). We also appreciate the assistance in the data analysis from Dr. Liyuchun in the State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, China. Y.C. and Y.J.L. conceived and designed study concept. Y.C., L.G., X.Y.L. and X.S.C. collected the samples and performed the experiments. Y.C. analyzed the data. Y.C. drafted the manuscript. S.H.Y. and Y.J.L. provided critical revisions. All authors approved the final version of the manuscript for submission. The authors used mitochondrial sequence data in Genbank, all the sequence data could be downloaded as Genbank number indicating from National Center of Biotechnology Information. All other relevant data are provided in the paper and Supporting files. The authors declare no competing interests.	3	3	[ -0.0166015625, 0.026123046875, -0.000759124755859375, 0.03515625, -0.004302978515625, 0.0048828125, -0.02001953125, -0.0140380859375, 0.01348876953125, 0.043212890625, 0.005218505859375, -0.01361083984375, -0.01104736328125, -0.01080322265625, 0.003326416015625, -0.02587890625, 0.00982666015625, -0.029052734375, 0.00823974609375, -0.004669189453125, 0.00787353515625, -0.0007476806640625, -0.004486083984375, 0.00109100341796875, -0.003570556640625, 0.000614166259765625, 0.0201416015625, -0.0078125, -0.00958251953125, -0.017822265625, 0.0084228515625, 0.032470703125, -0.0260009765625, -0.00131988525390625, -0.0169677734375, 0.01123046875, -0.017578125, 0.004913330078125, -0.041259765625, -0.0184326171875, -0.0024261474609375, 0.0208740234375, -0.0019683837890625, 0.00775146484375, 0.01446533203125, -0.00970458984375, 0.01007080078125, 0.01373291015625, 0.00008726119995117188, -0.025146484375, -0.0130615234375, 0.0074462890625, 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Q: Literal Assignment in Java what's the difference in defining double example = 23.1d or double example = 23.1 Why long, float and double can end with l, f, d? A: There is no difference between double example = 23.1d; and double example = 23.1; because a floating point literal without a type suffix is always interpreted as a double. The type suffixes are necessary in order to avoid ambiguities in certain scenarios. For example, java supports method overloading. This means that you can have void x( float f ); and void x( double d ); Both methods are called x; which one will be selected depends on the type that you pass; if you pass a variable which is already known to be either float or double, things are clear; but if you want to pass a literal, like this: x( 5 ); then you have to be able to specify whether you mean this 5 to be a float or a double, so as to select the right method. There are a few other very nuanced situations where the type of the literal matters. For example, the following code: System.out.println( "" + (2/3.3333) ); System.out.println( "" + (2/3.3333f) ); Yields the following output: 0.6000060000600006 0.600006 ...because the first number is a double, while the second number is a float. Similar disambiguation concerns make the "L" type suffix necessary for long integer literals.	3.75	4	[ -0.0031890869140625, -0.016845703125, -0.01544189453125, 0.0166015625, -0.01312255859375, -0.032470703125, -0.020263671875, 0.0115966796875, -0.0137939453125, -0.0011444091796875, -0.00408935546875, 0.002471923828125, -0.03173828125, -0.0166015625, 0.00009441375732421875, -0.0079345703125, -0.00872802734375, -0.0032196044921875, 0.005828857421875, -0.01336669921875, 0.06884765625, 0.00555419921875, 0.005157470703125, 0.01312255859375, -0.005035400390625, -0.0255126953125, -0.002471923828125, -0.0172119140625, 0.01153564453125, -0.0162353515625, 0.01214599609375, 0.005645751953125, -0.03369140625, 0.00064849853515625, 0.005462646484375, 0.00775146484375, 0.0216064453125, 0.0167236328125, 0.0084228515625, 0.00150299072265625, 0.00897216796875, -0.0255126953125, -0.01165771484375, 0.01080322265625, -0.001983642578125, -0.007720947265625, 0.00811767578125, 0.0152587890625, 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Stretchable electronics, an emerging class of modern electronic materials that can bend and stretch, have the potential to be used in a wide range of applications, including wearable electronics, "smart skins" and minimally invasive biomedical devices that can move with the body. Today's conventional inorganic electronic devices are brittle, and while they have a certain flexibility achieved using ultrathin layers of inorganic materials, these devices are either flexible, meaning they can be bent, or they are stretchable, containing a discrete LED chip interconnected with stretchable electrodes. But they lack "intrinsic stretchabilty," in which every part of the device is stretchable. Now, researchers at the UCLA Henry Samueli School of Engineering and Applied Science have demonstrated for the first time an intrinsically stretchable polymer light-emitting device. They developed a simple process to fabricate the transparent devices using single-walled carbon nanotube polymer composite electrodes. The interpenetrating networks of nanotubes and the polymer matrix in the surface layer of the composites lead to low sheet resistance, high transparency, high compliance and low surface roughness. The metal-free devices can be linearly stretched up to 45 percent and the composite electrodes can be reversibly stretched by up to 50 percent with little change in sheet resistance. Because the devices are fabricated by roll lamination of two composite electrodes that sandwich an emissive polymer layer, they uniquely combine mechanical robustness and the ability for large-strain deformation, due to the shape-memory property of the composite electrodes. This development will provide a new direction for the field of stretchable electronics. This research was recently published in the peer-reviewed journal Advanced Materials . 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Curriculum Bank Lesson searchable by grade and subject. Often include videos Gooru is a search engine for learning that allows you to explore and study over 2,600 standards-aligned and personalized study guides. Study guides cover 5th-12th grade math and science topics, and resources include digital textbooks, animations, instructor videos and more. All resources are vetted and organized by teachers or Gooru’s content experts, so you don’t have to sort through the mess of subpar educational resources available online yourself. Learn Zillions Math videos for grades 3-9. Created by teachers. Option to create playlists for individual students and assessments. Mathtrain.TVThese video math tutorials were created for students by students from Lincoln Middle School (Santa Monica, CA). Sixth graders have created nearly one hundred clips, most of them less than two minutes in run time. NuskoolThis is a site that uses pop culture as teaching moments for students. Tailored to grades 6th-12th students learn a variety of subjects such as: Math, Science, English, etc through educational lessons based on the different elements of pop culture (video games, sports, films, etc.). Math Liveis a neat mathematics website hosted byLearn Alberta. Math Live presents students with animated stories that teach mathematics lessons. In all there are twenty-three lessons for elementary school and middle school students. The lessons are divided into four categories; Number, Patterns and Relations, Shape and Space, Statistics and Probability. Each animated lesson is accompanied by a mathematics worksheet that students complete either while watching the lesson or after viewing the lesson. Each lesson is divided into sections and students can advance or rewind as needed. mySkillBoard is a nice new site for differentiating instruction. The way this is done is by an educator inputing student data into mySkillBoard and then being able to assess students through different visualizations. Also, an educator can align student skills to Common Core Standards and even use it on any mobile device. PBS Math Clubis a YouTube channel in which students can watch and interact with math videos. Each of the videos contains a series of math lessons and challenge activities. To complete a challenge students click on the video to answer questions. If they answer correctly, they move on to the next question. If they answer incorrectly students are shown another video clip that explains the correct answer. LearnBop- A great site for educators teaching Math in grades K-12 that tracks student progress and allows educators to differentiate instruction.Math Is Power 4 U. Math Is Power 4 U is a large collection of tutorial videos primarily covering topics found in middle school and high school math courses. The videos are short and direct. You could make very similar videos yourself, if you wanted to. The best aspect of Math Is Power 4 U is the searchable database of videos. The database, hosted by Phoenix College, makes it easy to quickly find a video explaining topics in arithmetic, algebra, geometry, calculus, and half a dozen other topics. MathsMastervideos on a range of topics. See videos about the basic four operations up to complex algebra graphs. Each video is presented in a slow, step by step,student friendly way. These videos are great as an introduction to a topic or forhome study. Plus Magazineis an internet magazine which aims to introduce readers to the beauty and the practical applications of mathematics. Plus provides articles and podcasts on any aspect of mathematics and it also features review of math books and well as challenging math puzzles. Knewton.The company believes its new, free online tutoring platform will radically transform how teachers personalize instruction. Knewton claims to offer automated, digital tutoring that responds to each student's needs. "We can take the combined data power of millions of students — all the people who are just like you — [who] had to learn a particular concept before, that you have to learn today — to find the best pieces of content, proven most effective for people just like you, and give that to you every single time," he says. Here's how it works: The platform presents video and a variety of written content and then asks multiple-choice questions. Based on student responses, and patterns of responses from other, similar students, the next piece of content is served up. ModMath ( app) is an adaptive program that improves math skills. The app lets you type math problems right onto the touch screen of an iPad rather than write them out long-hand. You can then solve the problems using the touch pad and print or e-mail the assignments all without ever picking up a pencil. Prodigy- A free online Math game aligned to Common Core Standards grades 1-6th. Best of all this game differentiates instruction and educators can track students' progress as well as generate detailed reports. Sports Science - Awesome collection of short videos that will engage kids in science and math from the people at ESPN.ScootPad is a math and reading practice platform for elementary grades (K-5). Self-paced and personalized practice on ScootPad keeps kids engaged & challenged. ScootPad is Free. Buzz Mathis the latest interactive math workbook which provides middle school students with immediate detailed feedback, examples, and motivation to allow them to progress at their own pace. Motion Math Gamesdesigns challenging math games to sharpen your kids mathematical wits. It also has a mobile version to install on your iPad. IXL - One of the most popular sites around for Math that allows for student tracking w/ detailed reporting. Also, w/ the ability to track student "trouble" areas a teacher can adjust their teaching to help meet the needs of their students. iPracticeMathis a site for educators or students looking to teach, learn, or reinforce their math skills. Geared towards K-12, iPracticeMath covers a wide variety of subjects such as: Geometry, Algebra, Fractions, etc. Also, iPM has an abundance of resources for educators/students to use such as: worksheets, problem walkthroughs, glossary, and more. Best of all a registered educator/parent can get detailed reporting and track student progres Exampl : Get unstuck with homework Get instant homework help with Exampl! Take a photo of your problem to get help from your peers. You can even annotate your question, add a voice note, and tag it with a specific subject, like Algebra. Once your question has been solved, you can help other students too! No more typing elaborate solutions when you help others. It takes another photo or annotation to help others. KnowRe is a site for learning Math. Students can learn at their own pace and earn rewards such as digital badges for accomplishments. A nice feature for teachers is that is is aligned to common core standards and teacher can track and get real-time results on student data.XtraMath Its goal is to develop effective, efficient, adaptive and intrinsically rewarding supplemental math activities and make them available for free. myMathUniverse (gr 5-8) site with videos to help students with math homework and challenge them with new problemsmyMathUniverse. Supports middle grades math program, digits, a curriculum written entirely to the Common Core State Standards (CCSS) which leverages technology to personalize student learning and optimize class instructional time. Manga High, a collection of casual online math games developed using the Japanese manga style of animation Virtual Nerd, which lets students choose their own path through math content with step-by-step tutorials and a dynamic whiteboard Media 4 Math has a nice regular feature called Math in the News. Math in the News offers ideas for short mathematics lessons based on current news stories. TenMarks - A common core aligned program for Math (grades 1st-10th) that uses differentiated instruction to help students learn. Math Live presents students with animated stories that teach mathematics lessons. In all there are twenty-three lessons for elementary school and middle school students. The lessons are divided into four categories; Number, Patterns and Relations, Shape and Space, Statistics and Probability. Each animated lesson is accompanied by a mathematics worksheet that students complete either while watching the lesson or after viewing the lesson. Each lesson is divided into sections and students can advance or rewind as needed. Buzz Math is not a completely free to use tool, but they do have a free option that makes it worth checking out! Right now, you can subscribe one class for free for the school edition of Buzz Math. Buzz Math is intended for students in Middle School math. All of the activities are directly tied to Common Core Standards. You can assign activities based on a specific standard for the whole class, or just assign the activity to individual students. You get feedback immediately as students complete an activity so that you can plan instruction accordingly. These are not your typical math site activities (online multiple choice). Instead, each activity is a little different, highly engaging, and provides students with great feedback. Gummii - An innovative site (private alpha)/app for different areas of Math (fractions, addition, subtraction). Gummi immerses students into a educational 3D world (similar to Minecraft) where they solve mathematical equations tailored to differentiated instruction. 101 Questionson which he is sharing images and videos as prompts for developing math questions. TenMarksoffers a free online mathematics program designed to supplement your in-classroom mathematics instruction. The free TenMarks program covers materials for students in grades two through ten. In the program there are more than 2,000 video lessons available to students to view on demand. Teachers can use the TenMarks program to assign lessons and problems to individual students or to an entire class. Teachers can track the progress of individual students and the progress of an entire class. Yummy Math is a website designed for the purpose of sharing mathematics problems and scenarios based on things happening in the world today. For example, the activity for December 4th was based on Lebron James's return to Cleveland. Yummy Math lists activities chronologically as well as by mathematics subject area. Two mathematics teachers, Brian Marks and Leslie Lewis, developed Yummy Math and welcome suggestions from other mathematics teachers. Math PickleA nice site for locating videos and exercises appropriate for teaching a variety of mathematics concepts at a variety of grade levels. When you visit Math Pickle you can browse for videos by grade level. Once you've selected a grade level you can then refine your browsing to a particular concept. Each concept has a demonstration video and links to Keynote and Powerpoint files for teachers. Each concept also has links to PDF worksheets that you can download and print. MathVidsath videos about tough Math concepts starting with pre-algebra through high school math Desmos includes support for graphics, photos, math tools, and interactive lessons. You can create math lesson using the math tools, including graphing and equations. You can also the graphics program to create interactive diagrams where students can move the labels themselves. Math Open Reference is a free online reference for geometry teachers and students. It features animated and interactive drawings to demonstrate geometry terms and concepts. The table of contents is divided into four basic categories; plane geometry, coordinate geometry, solid geometry, and function explorer tools. Click on any subject in the first three categories to find definitions, examples, and interactive drawings. In the function explorer category users can select linear functions, quadratic functions, or cubic functions to explore how changes in variables affect the graphed output. Manipulatives Math Tool Chest- fun math interactives for any kid Useful for smartboards also PBS Learning Media has a free service called Learning Media. Resources include pictures, video and interactive materials from a robust library of high-quality digital content from PBS, and a growing list of other contributors including the National Archives, Library of Congress and NPR. There are research-based resources, including videos, interactives, images, audio files and lesson plans. You can view three resources. Then you have to create an account which is free. Can be filtered by grade level (Pre-K to 12+), subject (8), media type (document, audio, video, etc.), language (5) and accessibility (text, audio description, display transformation, etc). Audacity This site provides a nice set of maths tools for whiteboards. Whilemost whiteboard software have these tools, can you ever find themwhen you want them? Another benefit of this resource is that this will work on any Pattern Maker Looking for a way to help your students build their spatial sense? Pattern Maker – a special combination of art and geometry -- might be just the right tool for you. Students can flip, slide, turn, scale, and tessellate colorful objects, creating patterns of their own imagination or copying pre-selected patterns. Finishing a pattern triggers a brief question for the student to answer, based on the geometric techniques used and linked to key terms in a Shape Dictionary. Mangahighcreates exceptionally high-quality, game-based learning resources to help Primary and Secondary students reinforce their Mathematics skills in a way that is both fun and engaging. In addition to all the great resources, the service includes assessment and analytical tools that enable teachers to monitor the progress of individual students. Best of all, these activities also work great on the SMART Board Interactive Whiteboard. Calendar Clowns(gr. 1-3) Games teaches how to navigate a calendarRounding Master(gr. 2-5)Rounding off game in a Who Wants to be A Millionaire formatGarage Sale Wizard (gr 1-3) You play the role of a cranky old man trying to make a few bucks by selling his stuff at a garage sale. For each item, there will be three people vying for its purchase. Each person will offer a different amount of money. Count up the coins and click on the person who offers the best deal (the most money). Charts Graphmaster - Graph Master is a program is a one-of-a-kind program that allows students to create three different interactive, printable graphs on one screen based on data collected in a survey or poll of their classmates. What makes Graph Master so useful, however, is the fact that after students make their graphs, the program asks them eight multiple choice questions about their graphs using the inputted data. Hohli Online Charts Builderis a nice tool for creating a variety of charts for online display. Using the Hohli Online Charts Builder you can create bar graphs, line graphs, pie charts, Venn diagrams, scatter plots, and radar charts. Your chart will be generated as you enter information so that you can see how each piece of information influences the chart. When you're satisfied with your chart just click on it to save it to your computer or to grab the embed code to use on your blog or website. Because the charts update as each new piece of data is added, students will be able to see how each data set they add affects their chart's display. Cacoo- Nice site for creating online charts and graphs with a built-in chat feature for collaboration. Plus Magazine is a free online publication dedicated to introducing readers to practical applications of mathematics. Plus Magazine strives to reach that goal through the publication of mathematics-related news articles, podcasts, and mathematics puzzles designed around "real-life" scenarios. Gooruis a service that aims to provide teachers and students with an extensive collection of videos, interactive displays, documents, diagrams, and quizzes for learning about topics in math and science. Access to hundreds of resources according to subject areas such as chemistry, biology, ecology, algebra, calculus, and more. Within each subject area you can look for resources according to media type such as video, interactive display, slides, text, and lesson plans. Dynamic Paper Need a pentagonal pyramid that's six inches tall? Or a number line that goes from 18 to 32 by 5's Or a set of pattern blocks where all shapes have one-inch sides? You can create all those things and more with the Dynamic Paper tool. Place the images you want, then export it as a PDF activity sheet for your students or as a JPEG image for use in other applications or on the web. Mathematics in Moviesis a website developed by Oliver Knill, a Harvard Mathematics professor. Mathematics in Movies is a collection of video clips from popular movies and television shows in which references to mathematics are made. One clip that I enjoyed comes from an episode of The Office in which Oscar tries to explain the concept of a budget surplus to Michael. Study Jams is a Scholastic website designed to help elementary school students learn and review math and science information through songs and videos. To use Study Jams students search for a topic in the math or science category. Each Study Jam offers a short tutorial on that topic in the form of a video, slideshow, or song. When there is a song available Study Jams provides a karaoke format for kids to sing along if they like. EaselAlgebra ilite - Easel combines interactive, hands-on algebra workbooks with instant "ShowMe" lessons. If you get stuck on a problem, just tap "ShowMe" and see a step-by-step animation of how to solve the problem. Algebra 4 All A social network dedicated to algebra teachers. At Algebra 4 All (A4A), teachers support one another in the practice of teaching algebra Math Open Reference is a free online reference for geometry teachers and students. Math Open Reference features animated and interactive drawings to demonstrate geometry terms and concepts. 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Q: Break if statement in python i have mistake with my python code. There's mini game about guessing code. i want to break if statements and make else statement (activated when i guess wrong letter).Here's the code. Return and break function outputs: "return/break function outside the loop". Please, modify the code :D ` import time print('Oto jest gra, w której musisz odgadnąć kod! Kod ma 4 litery!') decyzja = input('Chcesz grać? T/N\n') if decyzja == "t" or "T": one = input('Wpisz 1 litere\n') if one == "k": two = input('Wpisz 2 Litere\n') if two == "u": three = input('Wpisz 3 litere\n') if three == "b": four = input('Ostatnia!\n') if four == "a": time.sleep(2) print('Zgadles kod!!!') ` A: Try this (it's better to use a function): import time def numguess(myinput): if decyzja.lower() == "t": one = input('Wpisz 1 litere\n') else: return False if one == "k": two = input('Wpisz 2 Litere\n') else: return False if two == "u": three = input('Wpisz 3 litere\n') else: return False if three == "b": four = input('Ostatnia!\n') else: return False if four == "a": time.sleep(2) print('Zgadles kod!!!') else: return False print('Oto jest gra, w której musisz odgadnąć kod! Kod ma 4 litery!') decyzja = input('Chcesz grać? 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Electrical circuits requiring high power handling capability (>20 watts) while operating at high frequencies such as radio frequencies (500 MHz), S-band (3 GHz) and X-band (10 GHz) have in recent years become more prevalent. Because of the increase in high power, high frequency circuits there has been a corresponding increase in demand for transistors which are capable of reliably operating at radio frequencies and above while still being capable of handling higher power loads. To provide increased power handling capabilities, transistors with a larger effective area have been developed. However, as the area of a transistor increases, the transistor, typically, becomes less suitable for high frequency operations. One technique for increasing the area of a transistor while still providing for high frequency operations is to use a plurality of transistor cells that are connected in parallel. Such may be provided using a plurality of gate fingers, thus, the source to drain distance may be kept relatively small while still providing for increased power handling capability. Conventionally, when a plurality of parallel transistor cells are connected in parallel on a single chip, the cells are evenly spaced such that the gate-to-gate distance between adjacent cells (referred to herein as “pitch” or “gate pitch”) is uniform. When such multi-cell transistors are used in high frequency operations, they may generate a large amount of heat. As a device heats up, performance of the device typically degrades. Such degradation may be seen in gain, linearity and/or reliability. Thus, efforts have been made to keep junction temperatures of the transistors below a peak operating temperature. Typically, heatsinks and/or fans have been used to keep the devices cool so as to ensure proper function and reliability. However, cooling systems may be increase size, electrical consumption, costs and/or operating costs of systems employing such transistors. With uniform pitch multi-cell transistors, the temperature of cells near the center of the array are typically greater than those of the cells at the periphery. This is generally the case because the cells at the periphery have a larger area and/or a greater thermal gradient to areas surrounding the cells. Thus, for example, adjacent cells near the center of the multi-cell array will each generate heat and thus, each side of the cells will be at an elevated temperature with respect to cells farther from the center. This results in a thermal profile that is roughly a bell curve with center junction temperatures being the hottest and with the outer most junctions having a substantially reduced operating temperature compared to the center junctions. An uneven temperature distribution among the junctions of a device may reduce device linearity. For example, for a device with a plurality of evenly spaced gate fingers connected by a manifold, RF phasing errors may occur along both the gate manifold and the individual gate fingers as a result of differing gate resistance as a function of temperature. Conventionally, to address these issues the spacing between the gate fingers is widened and/or the length of the fingers are shortened and additional fingers added to achieve the same net active area. Both of these solutions may result in spreading the heat load generated in the center of the device over a wider area. These solutions also may result in a larger area for the multi-cell transistor that may reduce the number of die per wafer.	3.296875	3	[ 0.00091552734375, 0.00177001953125, 0.0145263671875, -0.00714111328125, -0.0205078125, -0.0218505859375, -0.00299072265625, 0.0126953125, -0.001129150390625, -0.0247802734375, 0.006622314453125, 0.0020599365234375, -0.00872802734375, 0.0079345703125, -0.01458740234375, -0.0001316070556640625, -0.003570556640625, 0.01055908203125, -0.0002803802490234375, 0.0135498046875, 0.058349609375, 0.00848388671875, -0.01129150390625, 0.0029144287109375, 0.0036468505859375, -0.013427734375, 0.00579833984375, 0.006744384765625, 0.018798828125, 0.016357421875, 0.00927734375, 0.005035400390625, -0.0272216796875, 0.009033203125, -0.00121307373046875, 0.004791259765625, 0.00921630859375, 0.0021209716796875, 0.007568359375, -0.044921875, -0.00994873046875, -0.0233154296875, 0.0177001953125, -0.0098876953125, -0.01544189453125, -0.0201416015625, 0.0126953125, 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Q: How to identify Enantiomers AP Biology Question So I know that enantiomers are like mirror images of each other, but not identical (superimposable) upon one another. On Wikipedia, I read that it was like our hands, similar but not identical (you can't rotate one hand into another. Makes sense. But I'm not sure how this would help me identify the enantiomers. All the molecules look identical. The answer is (D). What is different about D? A: The key point is that for four of the five pairs, the structure on the left can be rotated to make a structure exactly like the one on the right. For example, the left structure in (A), if rotated 120° about the C-CO$_2$H bond, is equivalent to the structure on the right. For two "enantiomeric" structures, it is not possible to do this. It might be helpful to draw every possible rotation of the structures in (D), to see that it is impossible to produce the structure on the right by rotating the one on the left.	3.46875	3	[ -0.0103759765625, -0.019287109375, 0.001953125, -0.006683349609375, 0.00396728515625, -0.0115966796875, -0.0026092529296875, -0.0130615234375, 0.0033416748046875, 0.02392578125, 0.0022430419921875, 0.00141143798828125, -0.026123046875, -0.004669189453125, 0.0037384033203125, -0.0166015625, -0.000125885009765625, 0.006744384765625, 0.013671875, -0.0020294189453125, 0.06591796875, -0.004180908203125, -0.00555419921875, -0.00946044921875, 0.0037689208984375, -0.00811767578125, 0.0012969970703125, -0.006500244140625, 0.0098876953125, -0.004364013671875, -0.005767822265625, 0.0125732421875, -0.03466796875, 0.00165557861328125, 0.00830078125, 0.0115966796875, 0.00909423828125, 0.007720947265625, -0.0037689208984375, -0.011962890625, -0.000701904296875, -0.0030364990234375, 0.003875732421875, 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One goal of semiconductor fabrication is to increase the density of active elements provided on an integrated circuit. In order to accomplish this, ongoing investigation in advanced lithography is underway to decrease the critical dimensions of active elements used to form these integrated circuits. Current lithography uses energy sources that include i-line at 365 nanometers and deep ultra-violet (DUV) at 248 nanometers to pattern substrate features. Decreasing the wavelength of the energy source allows for the formation of photoresist features having smaller critical dimensions. Accordingly, smaller wavelength energy sources are being developed as alternatives to conventional lithography. These include x-ray, ion projection, extreme ultra-violet (EUV) at 13.4 nanometers, and scattering with angular limited projection in electron-beam lithography (SCALPEL). SCALPEL and x-ray lithography masks are formed of attenuating elements overlying thin membranes. The membrane thickness of a SCALPEL mask is typically in range of 100-150 nanometers and the membrane thickness of an x-ray ray mask is typically in a range of 2000-5000 nanometers. Cleaning such masks is relatively difficult and presents numerous problems. Conventional wet chemical processes do not adequately remove particles without reacting with or damaging the mask. Physical agitation, such as ultrasonic agitation, is generally undesirable because of the delicate nature of the membranes. Other cleaning techniques, such as dry laser cleaning and frozen ice cleaning, are likely to be ineffective at adequately cleaning the masks, particularly when attempting to remove particles between patterned mask features. Conventional lithography has adopted the use of pellicles to protect masks from particles and to prevent the imaging of defects onto the semiconductor substrate. However, the use of pellicles in SCALPEL and x-ray lithography is problematic. The pellicle increases the thickness of material through which the energy must pass, thereby reducing throughput and increasing chromatic aberration. Additionally, contaminants or particles deposited on pellicles used in SCALPEL and x-ray lithography may nevertheless be imaged onto the resist, unlike in conventional lithography. Development in the field of self-assembled monolayers (SAMs) has been underway for several years. The particularities of commonly formed SAMs are disclosed in technical literature, including "Formation and Structure of Self-Assembled Monolayers", by Abraham Ulman, Chemical Reviews, Vol 96, 4, (1996) 1532-1544, and "An Introduction to Ultrathin Organic Films: From Langmuir-Blodgett to Self-Assembly" by Abraham Ulman, Academic Press, Inc., Boston (1991) 237-304, both of which are hereby incorporated by reference.	3.046875	3	[ 0.0052490234375, 0.00061798095703125, 0.000873565673828125, 0.02001953125, -0.00494384765625, -0.00653076171875, 0.00093841552734375, 0.00811767578125, -0.0145263671875, 0.0162353515625, 0.001739501953125, -0.0022735595703125, -0.00823974609375, 0.01531982421875, -0.021728515625, 0.00946044921875, 0.0031890869140625, 0.009765625, 0.00086212158203125, -0.00138092041015625, 0.006500244140625, 0.00164794921875, 0.03955078125, 0.007171630859375, -0.01153564453125, -0.0028076171875, 0.01470947265625, 0.00823974609375, -0.002349853515625, 0.003662109375, 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• The ExoMars Schiaparelli Lander (Entry, Descent, and landing Module, or EDM) crashed on the Martian surface on 19 October 2016. Also on that day the Trace Gas Orbiter successfully entered Mars orbit. The HiRISE images acquired soon after the crash showed diffuse dark markings surrounding a shallow crater, plus small bright spots. HiRISE re-imaged this location on 25 March 2019, while dust was still settling from the planet-encircling dust storm, so surface features had low contrast.HiRISE re-imaged this spot again through a much clearer atmosphere on 14 December 2019 ( see animation ). Much of the diffuse dark material has faded, perhaps from dust fallout, such that the crater is now more distinct. At least two bright spots are still visible.In 2020 we expect three launches to Mars leading to landing attempts in early 2021: NASA’s unnamed (Mars 2020) rover, that will collect samples for return to Earth; the ESA/Roscosmos ExoMars lander and Rosalind Franklin rover; and an orbiter, lander, and Huoxing-1 (Mars-1) rover from China. HiRISE will be ready to see what happens.Written by: Alfred McEwen (29 January 2020)	3.125	3	[ -0.013427734375, -0.00341796875, 0.006195068359375, 0.0025787353515625, 0.009033203125, -0.0050048828125, -0.00112152099609375, -0.0093994140625, -0.016357421875, -0.018798828125, 0.0037384033203125, -0.0023651123046875, -0.0247802734375, 0.0005035400390625, 0.00653076171875, -0.0096435546875, -0.01953125, 0.018310546875, -0.00970458984375, -0.0025177001953125, -0.017578125, 0.01806640625, -0.0028076171875, 0.00421142578125, 0.00811767578125, 0.01153564453125, 0.000339508056640625, -0.033447265625, 0.00153350830078125, -0.00119781494140625, 0.004302978515625, -0.008544921875, 0.0026397705078125, -0.003265380859375, -0.0038299560546875, -0.00830078125, -0.00732421875, 0.0186767578125, 0.004180908203125, -0.029296875, -0.003448486328125, 0.001708984375, 0.005859375, 0.0081787109375, -0.0181884765625, -0.006561279296875, 0.0137939453125, 0.0089111328125, 0.002227783203125, 0.012451171875, 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Contents >> Leading Causes of Death >> Overview - Leading Causes of Death OVERVIEW Ranking causes of death is a useful method of describing patterns of mortality in a population. It allows comparison over time and between populations. However, different methods of grouping causes of death can result in a vastly different list of leading causes for any given population. For this reason ABS ranks leading causes of death in this publication based on research presented in the Bulletin of the World Health Organization, Volume 84, Number 4, April 2006, 297-304 . For further information see Explanatory Notes 41-43. In 2011, the leading underlying cause of death for all Australians was Ischaemic heart disease (I20-I25), which includes angina, blocked arteries of the heart and heart attacks. Ischaemic heart diseases were identified as the underlying cause of 21,513 deaths, 14.6% of all deaths registered in 2011. While Ischaemic heart diseases have been the leading cause of death in Australia since 2000, the proportion of deaths due to this cause has decreased, from 19.5% (26,063) in 2002 to 14.6% (21,513) in 2011. Cerebrovascular diseases (I60-I69) have remained the second leading underlying cause of death in 2011. Cerebrovascular diseases include haemorrhages, strokes, infarctions and blocked arteries of the brain. Over the last 10 years, deaths due to this cause have decreased by 10.2%, from 12,533 deaths in 2002 to 11,251 deaths in 2011. Dementia and Alzheimer's disease (F01, F03, G30) was the third leading cause of death in 2011. The number of deaths due to this cause has increased by 126% over the past decade from 4,364 in 2002 to 9,864 in 2011. This is largely due to an increase in deaths due to Dementia (F01, F03), which increased from 2,513 in 2002 to 6,877 in 2011. For further information see Explanatory Note 84. Trachea, bronchus and lung cancers (C33-C34) were the fourth leading cause of death in 2011. Over the last 10 years, deaths due to this cause have increased by 11.1%, from 7,303 in 2002 to 8,114 in 2011. The top 10 leading causes of death accounted for 52% of all deaths registered in 2011, and the top 20 leading causes accounted for 67.2%. 2.1 LEADING CAUSES OF DEATH (a) , Australia - Selected years - 2002, 2006, 2011 (b) 2002 2006 2011 Cause of death and ICD code no. Rank no. Rank no. Rank Ischaemic heart diseases (I20-I25) 26 063 1 23 132 1 21 513 1 Cerebrovascular diseases (I60-I69) 12 533 2 11 479 2 11 251 2 Dementia and Alzheimer disease (F01, F03, G30) 4 364 6 6 550 4 9 864 3 Trachea, bronchus and lung cancer (C33-C34) 7 303 3 7 353 3 8 114 4 Chronic lower respiratory diseases (J40-J47) 6 256 4 5 463 5 6 570 5 Diabetes (E10-E14) 3 329 9 3 669 8 4 209 6 Colon, sigmoid, rectum and anus cancer (C18-C21) 4 649 5 3 857 6 4 087 7 Blood and lymph cancer (including leukaemia) (C81-C96) 3 791 7 3 700 7 3 978 8 Heart failure (I50-I51) 3 367 8 2 902 11 3 488 9 Diseases of the urinary system (N00-N39) 2 887 11 3 197 9 3 386 10 Prostate cancer (C61) 2 852 12 2 951 10 3 294 11 Breast cancer (C50) 2 716 13 2 643 13 2 937 12 Influenza and pneumonia (J09-J18) 3 084 10 2 711 12 2 492 13 Pancreatic cancer (C25) 1 834 15 2 077 15 2 416 14 Intentional self-harm (X60-X84)(c) 2 320 14 2 118 14 2 272 15 Skin cancers (C43-C44) 1 462 17 1 648 17 2 087 16 Accidental falls (W00-W19) 629 38 1 288 20 1 845 17 Hypertensive diseases (I10-I15) 1 353 20 1 500 18 1 802 18 Cardiac arrhythmias (I47-I49) 1 226 21 1 280 21 1 612 19 Cirrhosis and other diseases of liver (K70-K77) 1 354 19 1 416 19 1 589 20 (a) Causes listed are the leading causes of death for all deaths registered in 2011, based on WHO recommended tabulation of leading causes. See Explanatory Notes 41-43 for further information. (b) See Explanatory Notes 81-99 for further information on specific issues relating to 2011 data. (c) Excludes Sequelae of suicide (Y87.0) as per the WHO recommended tabulation of leading causes. Care needs to be taken in interpreting figures relating to suicide. See Explanatory Notes 92-95. 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Breast Cancer is New Zealand’s 3rd most common cancer and in the US, almost 40,000 women died from breast cancer last year. Women are encouraged to self examine their breasts so that they become aware of any changes or lumps which may appear at which point they are advised to visit a medical professional where a clinical breast exam (CBE) will be carried out. This involves a doctor or a nurse using their hands to examine the patients breasts using their fingers to try and feel any lumps or bumps under the skin. If something is found, then the next step is to refer the patient to a mammogram or to have a biopsy. The big issue is that due to the poor sensitivity of the human hand, clinical breast exams typically don’t find a lump until they are 21mm in length, yet early detection is crucial as if a cancerous lump is found in the breast when it is only 10mm it improves a patient’s survival rate by more than 94% compared to patients that do not have early detection of tumours. In my Radio Live interview last week I discussed a new nanotechnology film that is being dubbed “electronic skin” which could help to create an image of objects that lie underneath breast tissue. Imagine a thin strip of plastic being placed over your breast and the doctor carrying out the breast examination over the strip creating a savable image of any lumps within your breast. A different doctor could then carry out the same test over a film a few months later and could compare it to the previous results. This type of reporting has not been possible using standard breast examinations because the results are qualitative and very much based on what the doctor feels and records which could vary by their experience level and touch sensitivity. Created by Chieu Van Nguyen and Professor Ravi Saraf from the University of Nebraska-Lincoln, this thin film was created and put to the test by placing lumps of objects inside a piece of silicone to simulate a tumour within the breast tissue. In lab tests, using the same amount of pressure that a doctor would use in a clinical breast exam, the thin film device was able to successfully identify lumps down to 5mm in diameter and up to 20mm in depth which far exceeded what human touch would be able to detect. The 150nm film was able to image subsurface objects in silicone identifying their shape and size. Image adapted from original paper Their research published in the journal American Chemical Society Applied Materials & Interfaces describes how their 150nm ‘skin’ is filled with alternating sandwich layers of gold and cadmium sulfide nanoparticles. These nanolayers have a constant bias of 18 volts across them and when the surface of the film was touched, the pressure from the finger touching them converted the local pushing force into a buckling within the film layers diverting the current. This film was connected to an electro-optical device which measured the change in current from the buckling and converted it to an optical signal where the variation in light emission created an image on a camera (as shown in the blue image on the right). So as amazing as this technology is, it’s still in the research stage. Ravi Saraf estimates that a prototype device could be made within a year at the cost of about $1.5 million however no reports have been made regarding and securing of funding for commercialisation yet. Sciblogs Archive Sciblogs is the biggest blog network of scientists in New Zealand, an online forum for discussion of everything from clinical health to climate change. Our Scibloggers are either practising scientists or have been writing on science-related issues for some time. They welcome your feedback! 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Introduction ============ The discovery of microsatellites, and other hypervariable genetic markers, has enabled the study of genetic differentiation and population subdivision at small scales (e.g. [@b57]), even down to the level of the individual (e.g. [@b7]; [@b51]; [@b52]). The information gathered can have important implications for conservation work intended to preserve genetic variation. The significance of this objective increased following the World Summit on Sustainable Development and the publication of the framework for action on biodiversity and ecosystem management, which identifies genetic variation as one of the three levels of biodiversity recommended for conservation ([@b76]). Information on the scale over which genetic differentiation occurs also has important implications for the management of natural resources and the potential for local adaptation. Studies into freshwater salmonid fishes have revealed that genetic differentiation can occur over very short distances within river catchments. This can be associated with physical barriers to movement, which can isolate populations that then differentiate by genetic drift ([@b33]). In addition, differentiation has also been noted where salmonids exist without such barriers, including populations of the many anadromous species that could potentially be linked by gene flow ([@b69]; [@b65]; [@b2]; [@b55]). As such, these species represent an interesting case for studying processes of population differentiation. Specifically, the propensity towards population subdivision appears linked to two key factors: (a) the well-known ability of salmonids to home back to specific natal rivers ([@b68]) and (b) the patchy distribution of spawning areas within rivers ([@b44]) that may act to restrict gene flow among fish in different areas of a river (although other processes e.g. extinction-recolonization dynamics have also been described; [@b47]). Amongst salmonid species, the brown trout (Salmo trutta) is typified by having a particularly complex within catchment genetic structure, with high levels of genetic differentiation and an apparent lack of correlation between genetic and geographic distance ([@b4]; [@b12]; [@b22]; [@b43]; [@b61]; [@b62]; but also see [@b8]; [@b19]). Recently there has been an increasing emphasis placed on understanding the deeper biological significance of this complex population structure and there is a need to understand the underlying evolutionary models that may explain the observed patterns of genetic differentiation, which also have important implications for the ecology of brown trout, as well as the conservation of genetic diversity and management of the species. However, brown trout are under pressure from habitat destruction, pollution, over-exploitation and stocking with non-native fish, i.e. local factors that may erode the high levels of genetic variation observed and cause the extinction of unique varieties and loss of unique traits ([@b22]). Although the River Dart is no exception to the pressures that threaten the persistence of brown trout at a local scale, it does drain a National Park and so benefits from a relatively high level of statutory protection. Regular electrofishing surveys undertaken by the Environment Agency (EA; the national regulatory body in England and Wales) suggest that numbers of brown trout within the River Dart are significant and stable, although there has been a negative trend since records began in the 1960s ([@b70]; [@b14]). Changes in land use have led to habitat degradation in the headwaters, although a major threat facing trout in the River Dart arises from both human mediated and natural acidification. The low pH values which characterize the River Dart, combined with the fact that brown trout may spawn in small rivers ([@b17]), may make Dart trout more susceptible to catastrophic events. In turn, this may lead to localized extinctions and recolonizations, with important implications for patterns of genetic differentiation among groups of brown trout ([@b28]; [@b47]). Alternatively, the naturally low pH of rivers on Dartmoor may actually have promoted the tolerance of high acidity in indigenous populations of trout, generating the potential for local adaptation ([@b72]). The purpose of this study was to investigate the population genetic structure of brown trout at the scale of a single river catchment and to reconcile the potential for environmental instability to cause localized extinction events (e.g. [@b47]; [@b37]; [@b44]) with the apparently stable trout numbers present in the River Dart. [@b24] have previously proposed three scenarios that form an appropriate framework for addressing this question. Under the member-vagrant model, nursery areas play a vital role in determining population structure and selection favours individuals that return to their natal spawning grounds to reproduce, which maximizes survival of the young and promotes the development of locally adapted gene pools. Thus, fish that complete this process of homing are considered 'members', contributing to local adaptation and those that do not return to natal areas are known as 'vagrants' ([@b34]; [@b24]). This model predicts temporal stability of population structure, a significant effect of isolation-by-distance and strong genetic differentiation among populations. Under the second model, the metapopulation model, the degree of genetic structuring depends on the temporal stability of habitats, so in an unstable environment the occurrence of locally adapted gene pools can be curtailed because of local extinctions (and subsequent recolonizations, reviewed in [@b3]; [@b41]; [@b59]). The key features of this model are that local populations (or subpopulations) are interconnected not only by migration but also recolonization and empty/unoccupied patches have an important role in metapopulaton dynamics. This model predicts that there would be lower levels of temporal stability in population structure, no significant effect of isolation-by-distance and lower genetic divergence between subpopulations (but still statistically significant because of founder effects, [@b24]; [@b41]; [@b59]). The third scenario is panmixia, where gene flow is unrestricted across the catchment and suggests the absence of genetic differentiation, such that neither of the previous two models applies. Elucidation of the evolutionary model appropriate to Dart trout offers the potential not only to aid local management and conservation, but also to begin to address the relative scarcity of population genetics research completed on salmonids in England and Wales. The present study examined the variability at nine microsatellite loci in brown trout sampled from the River Dart over a 3-year period, with the specific aim of ascertaining the pattern of genetic differentiation within a river system that is particularly vulnerable to severe pH depressions. The results from this analysis, which included application of the decomposed pairwise regression (DPR) method that allowed the relative strengths of genetic drift and gene flow to be accessed in each sample, were then used to consider which evolutionary model (member-vagrant, metapopulation or panmixia) best fitted the data. In addition, spatial autocorrelation was also employed to determine the geographic scale over which genetic differentiation occurred in Dart trout: the conservation implications of these results are discussed. Methods ======= The study area -------------- The River Dart catchment is located in Devon, southwest England ([Fig. 1](#fig01){ref-type="fig"}). It is approximately 75 km long, covers an area of 475 km^2^ and flows into the English Channel through the Dart Estuary and into Start Bay. The river rises on Dartmoor National Park, an upland granite mass that reaches over 600 m high. The catchment is a typical moorland system, characterized by high rainfall and a peaty, acidic soil. The area represents the largest unglaciated expanse of upland in Great Britain and the largest granite surface in England. There are no real aquifers on Dartmoor and water is primarily stored in wetlands and bogs. The river is formed from two main tributaries, the East and West Dart. The upper reaches support small-scale livestock farming, which becomes more intensive and incorporates arable farming once it flows off the moor. ![Map of the River Dart. Grey dots indicate sampling sites, which are accompanied by abbreviated sample names that match those in [Table 1](#tbl1){ref-type="table"}. Significant barriers to fish movement are indicated by double lines perpendicular to the river.](eva0002-0537-f1){#fig01} The catchment supports a locally important stock of resident and anadromous trout (see rod-catch data below), with all the tributaries and several stretches of the main river containing excellent spawning and nursery areas. In particular, many of the headwaters provide valuable spawning grounds, not only for brown trout, but also Atlantic salmon (Salmo salar L.). The river also supports a rod/game fishery, as well as a limited commercial estuary (seine) net fishery. Catches of sea trout in 2002, the year this study began, were 712 for rod catches and 727 for net catches ([@b15]). Formal records of brown trout stocking in the UK were first collected by the national river boards during the 1950s and show that in the period up to 2005, 145 212 individual ova, fry or smolt were stocked into the River Dart. These comprised 65 separate stocking events at a minimum of 18 discrete locations within the river. The largest single stocking incident was of 96 000 eyed ova into the headwaters of the East Dart in 1961 (this single event accounts for the majority of all recorded stocking on the River Dart). The source of most stocked trout is thought to be various local hatcheries from southwest England, but the ultimate origin of hatchery stocks has been impossible to uncover ([@b23]). In the last decade local fisheries groups have taken to stocking the lower reaches of the River Dart with much smaller numbers (in the hundreds) of hatchery reared smolt which are typically bred from trout of Dart origin. Sample collection ----------------- A total of l1225 brown trout of multiple year classes, but predominantly parr and excluding fry (to avoid collecting siblings; [@b30]), were collected by electrofishing from 22 sites spread across 14 tributaries within the River Dart catchment. Five of these sites were isolated above barriers; the Gata and the Ash above man-made weirs and the Rud group of samples above a natural waterfall ([Fig. 1](#fig01){ref-type="fig"}). The average in-water distance among sample sites was 22.7 km, with a range of 0.8--64.4 km. Sampling was carried out each summer (July--September), from 2002 to 2004 ([Table 1](#tbl1){ref-type="table"}; [Fig. 1](#fig01){ref-type="fig"}). The adipose fin was removed from each fish and preserved in 98% ethanol, after which the fish was released; removal of the adipose fin provided a permanent mark so the same individuals were not sampled again in subsequent years. ###### Sample site abbreviations Abbreviation Latitude Longitude Details Year n -------------- ------------ ----------- ---------------------------------- ------ ----- Amm 50°28′27″N 3°39:44″W Amm Brook, Amm house weir 2002 32 Ash 50°31′50″N 3°45′26″W Ashburn, Belford Hill 2002 36 Dury 50°35′06″N 3°53′26″W Dury Brook, Dury Farm 2002 33 EDar 50°35′44″N 3°54′49″W East Dart, Postbridge 2002 21 EWebB 50°35′21″N 3°48′27″W East Webburn, Bagpark Estate 2003 28 EWebD 50°34′12″N 3°48′40″W East Webburn, Dunstone Bridge 2004 57 EWebV 50°34′32″N 3°48′25″W East Webburn, Veton Bridge 2003 49 EWebW 50°35′08″N 3°48′26″W East Webburn, Wooder Manor 2002 25 EWebW 50°35′08″N 3°48′26″W East Webburn, Wooder Manor 2003 52 Gata 50°27′08″N 3°37′49″W Gatacombe River 2002 34 Har 50°25′55″N 3°46′54″W Harbourne, Hatcheries Fish Farm 2002 41 Hem 50°27′45″N 3°40′08″W River Hems 2002 40 Hol 50°30′15″N 3°49′47″W Holly Brook 2002 29 LChe 50°33′27″N 3°55′55″W Cherry Brook, Lower Bridge 2002 32 LChe 50°33′27″N 3°55′55″W Cherry Brook, Lower Bridge 2003 27 RudB 50°32′55″N 3°47′46″W Ruddycleave, Bowden Farm 2003 42 RudB 50°32′55″N 3°47′46″W Ruddycleave, Bowden Farm 2004 54 RudC 50°32′39″N 3°48′05″W Ruddycleave, Ruddycleave Cottage 2003 36 RudP 50°33′28″N 3°47′11″W Ruddycleave, Pudsham Down 2002 21 RudP 50°33′28″N 3°47′11″W Ruddycleave, Pudsham Down 2003 38 RudP 50°33′28″N 3°47′11″W Ruddycleave, Pudsham Down 2004 39 Swin 50°32′33″N 3°54′36″W River Swincombe, Wydemeet 2002 32 Swin 50°32′33″N 3°54′36″W River Swincombe, Wydemeet 2004 48 UChe 50°34′38″N 3°55′58″W Cherry Brook, Upper Bridge 2003 29 UChe 50°34′38″N 3°55′58″W Cherry Brook, Upper Bridge 2004 41 WDar 50°33′47″N 3°57′53″W West Dart, Cockern Tor 2002 39 WDar 50°33′47″N 3°57′53″W West Dart, Cockern Tor 2003 32 WDar 50°33′47″N 3°57′53″W West Dart, Cockern Tor 2004 48 Web 50°31′35″N 3°47′43″W River Webburn, Mistresses Piece 2002 32 WWeb 50°33′03″N 3°50′03″W West Webburn, Pondsworthy Bridge 2002 47 WWeb 50°33′03″N 3°50′03″W West Webburn, Pondsworthy Bridge 2003 32 WWeb 50°33′03″N 3°50′03″W West Webburn, Pondsworthy Bridge 2004 46 WWebL 50°34′26″N 3°51′02″W West Webburn, Lower Cator Bridge 2002 33 Location details, year of sample collection and numbers of fish sampled (n). See [Fig. 1](#fig01){ref-type="fig"} for locations. Microsatellites --------------- DNA was extracted from the fin tissue according to an ammonium acetate precipitation method, similar to that described in [@b5]. Genetic variation was determined at nine di-nucleotide microsatellite loci: Str15, Str60, Str73 ([@b18]), Str85 ([@b54]), SsoSL417, SsoSL25 ([@b64]), Strutta58 ([@b53]), SsoSL438 (A. Slettan, unpublished data, GenBank accession no. Z49134) and SsHaeIII.14.20 (J. L. Goodier unpublished, GenBank accession no. U10050). Genotypes were assayed through polymerase chain reaction (PCR) and polyacrylamide gel electrophoresis with fluorescently labelled primers. PCR reactions were carried out in 10 μL reaction volumes and standard PCR reagents were used in a mixture containing 10--100 ng DNA, 0.5 μ[m]{.smallcaps} of each primer, 1--1.5 m[m]{.smallcaps} MgCl~2~, 200 μ[m]{.smallcaps} of each dNTP, 1× reaction buffer and 0.5 U of Taq DNA polymerase (Bioline, London, UK). The PCR profile consisted of: a single denaturing set lasting 3 min at 94°C, 30 iterations of 94°C for 30 s, annealing temperatures 51°C (Str85), 52°C (Str15 & Sso417), 54°C (Sso25 & Strutta58), 58°C (SsHae), 60°C (Str 73) or 65°C (Str60) for 30 s and 72°C for 30 s with a single elongation step of 72°C for 10 min. However, the Sso438PCR profile was a stepwise program, with the annealing stage made up of six iterations at 1° intervals between 54°C and 48°C. For those loci producing weak products (SsHae, Str15 and Str73) 40 iterations were generally used. Size determination of the labelled PCR products was performed using a Beckman-Coulter (Fullerton, California, USA) CEQ8000 automated DNA sequencer with an internal size standard, according to the manufacturer\'s instructions. The raw data were analysed with the platform\'s-associated fragment analysis software (Beckman-Coulter). Genetic diversity analysis -------------------------- ARLEQUIN version 3 ([@b63]) was used to estimate the variance components in allele frequencies among years ([@b20]) and all samples were found to exhibit temporal stability (see Results). Therefore, in subsequent analyses temporal samples from a location were combined to estimate population allele frequencies, as recommended by [@b75]. Each sample at each locus was tested for conformity to Hardy--Weinberg equilibrium (HWE; [@b26]) using GENEPOP 3.4 ([@b56]) and any deviations were further investigated with Microchecker ([@b46]). Critical levels of significance for simultaneous tests were adjusted using the sequential Bonferroni procedure for multiple tests ([@b58]). In addition, Powermarker version 3.25 ([@b40]) was used to calculate expected and observed heterozygosity, and FSTAT version 2.9 ([@b25]) was used to calculate allelic richness (allele number corrected for sample size using the rarefaction method of [@b16]) and the inbreeding coefficient. To examine the levels of genetic differentiation between pairs of samples a test of the homogeneity of allele frequency distributions (the so-called test of 'genic differentiation') was run in GENPOP ([@b56]) and F~ST~ values were calculated ([@b77]) in ARLEQUIN. Critical levels of significance for simultaneous tests were adjusted using the sequential Bonferroni procedure for multiple tests ([@b58]). The chord distance (D~CE,~[@b10]) was also used to quantify genetic differentiation between samples. This measure was chosen because the close proximity of samples included in the study means mutation is unlikely to have contributed to population divergence and the D~CE~ distance is based on geometric distances, which are independent of models of microsatellite mutation ([@b40]). It has also been shown to be one of the most efficient methods for obtaining correct tree topology using microsatellite data ([@b71]). Neighbour-joining (NJ) phylograms were constructed and confidence intervals on tree topology were estimated by bootstrap resampling of loci 1000 times utilizing the programs P[owermarker]{.smallcaps} version 3.23 ([@b40]), C[onsense]{.smallcaps} (from Phylip 3.6; [@b21]) and T[ree]{.smallcaps} V[iew]{.smallcaps} version 1.6 ([@b48]). Decomposed pairwise regression analysis --------------------------------------- To detect outlier populations and accurately elucidate patterns of isolation-by-distance, the DPR ([@b37]) was applied. The DPR can also estimate the relative strengths of genetic drift and gene flow for each sample, by decomposing the regression of the pairwise genetic and geographic distances ([@b60]). Briefly, genetic distance \[F~ST~/(1 − F~ST~)\] is plotted against geographic distance for all pairwise comparisons. Outlier analysis then determines which samples have exceptional characteristics that may falsely influence the pattern of IBD (e.g. founder effects, bottlenecks, physical barriers, all of which can strongly affect the overall pattern). These outlying samples were determined based on the systematic bias of the regression residuals (process one, which identifies 'putative' outliers). The outliers were then sequentially removed from the analysis and the best model was selected based on the AIC (Akaike\'s information criteria) value (process two, which identifies 'true' outliers); the smallest values indicate the most plausible model ([@b6]). Because of the small sample sizes, the corrected AIC (AIC~C~) was used. Finally, after determining the best model and the 'true' outliers, the pairwise genetic and geographic distances were regressed separately for each sample (including the outlier samples) against the nonoutlier samples, to investigate the different patterns of geneflow and drift. The significance of the relationship was assessed by ordinary least-squares regression. Spatial autocorrelation analysis -------------------------------- Spatial genetic structure was tested with the software package [genalex]{.smallcaps} version 6.1 ([@b50] and according to [@b55]). A Mantel test of matrix correspondence was used to examine the association between pairwise F~ST~ values and the in-water distance between sampling sites by estimating the r~xy~ measure that is analogous to an autocorrelation coefficient ([@b67]), with 999 permutations used to test the statistical significance of the values. At the scale of individual specimens, a multivariate microspatial autocorrelation approach was also employed ([@b66]; [@b51]). This test employed the squared distances measure (PhiPT; [@b51]) to estimate individual genetic distance, and the same in-water distances between sample sites used in the Mantel test for distance between individual specimens (with the exception that all individuals caught from the same sample site were assigned a distance value of zero). To assess the extent of nonrandom genetic structure among individuals ([@b51]), a correlogram of the autocorrelation coefficient (r) was plotted as a function of distance, specifically five distance classes: 0--5, 6--15, 16--25, 26--45, 46--65 km; a range of alternate distance classes from 5 to 25 km were also analysed. A multi-distance class (MDC) analysis was also used to give a more accurate estimate of the scale over which genetic structure was detected ([@b51]). In this approach the same classes as above were utilized, except that multiple analyses were performed with automatically increasing distance size classes, such that individuals from more distant classes were added to the previous groups ([@b51]). One thousand bootstrap replicates were used to ascertain the 95% confidence interval (CI) of the r estimates, and 999 permutations were used to resolve the 95% CI about the null hypothesis of no spatial genetic structure. Significant genetic autocorrelation was concluded when the CI of r and those of the null hypothesis did not overlap ([@b51]). Results ======= Genetic diversity ----------------- Pairwise testing of temporal samples revealed only one case of significant genetic heterogeneity between 2003 and 2004 samples at the RudB site in locus Strutta58 (P \< 0.05, corrected across loci; k = 9). Furthermore, quantitative estimates of hierarchical gene diversity across the whole dataset showed that while a significant amount of genetic variation (P \< 0.00001) was identified both within samples and among different sample sites (96% within samples and 4% between sites), a nonsignificant estimate of 0% variation was attributed to variation among temporal samples. Therefore, all temporal samples collected at individual sites were pooled in subsequent analyses. Genetic diversity indices for each locus and population are presented in [Table 2](#tbl2){ref-type="table"}. Significant deviations from HWE (P \< 0.05, corrected across loci; k = 9) for pooled samples were detected in two cases (EDar at SsoSL25 and EWebW at Str73). Further analysis of these cases with Microchecker did not reveal any evidence of null alleles or scoring errors, although the EDar case was associated with a significantly positive F~is~ value ([Table 2](#tbl2){ref-type="table"}), which could result from the nonrepresentative sampling of juveniles fish ('family sampling'; [@b1]; [@b30]; [@b78]). The mean number of alleles at a locus, across the whole dataset was 10.7 and ranged from 3 (Str60) to 27 (Str58). The mean number of alleles per locus within samples had an average of 6.6 and ranged from 4.4 (RudB) to 8.0 (Har). The allelic richness (the average allele number within samples, corrected for a minimum sample size of 16 in this case) was smaller, with an average of 5.5 and ranged between 4.0 (RudB) and 6.6 (Har). The average observed heterozygosity (H~O~) across all samples was 0.6 and varied from 0.55 (RudP) to 0.74 (Amm). ###### Microsatellite diversity indices of the samples collected from 22 sites and results of the Hardy--Weinberg equilibrium test Sample Indices SsHae Str15 Str58 Str60 Sso25 Sso438 Str73 Sso417 Str85 Mean -------- --------- -------- -------- ----------- -------- ----------- ----------- ---------- -------- -------- -------- Amm N 32 32 32 32 32 27 32 32 31 A 10 5 13 2 10 4 4 8 6 6.889 A~R~ 8.616 4.488 10.919 2 8.32 3.83 3.5 7.632 5.389 6.077 H~E~ 0.843 0.695 0.88 0.482 0.812 0.582 0.604 0.829 0.64 0.708 H~O~ 0.875 0.844 0.969 0.438 0.844 0.593 0.625 0.813 0.677 0.742 F~is~ 0.294 −0.198 −0.085 0.109 −0.024 0.001 −0.018 0.036 −0.041 −0.032 HWE −0.22 0.142 0.112 0.744 0.567 0.761 0.61 0.161 0.96 Ash N 36 33 35 36 36 36 34 35 36 A 9 5 11 2 8 3 5 9 5 5.889 A~R~ 7.51 4.223 8.22 2 6.494 2.606 4.955 6.997 4.138 5.238 H~E~ 0.824 0.671 0.644 0.277 0.766 0.155 0.74 0.782 0.639 0.611 H~O~ 0.916 0.667 0.657 0.277 0.805 0.111 0.823 0.828 0.722 0.645 F~is~ −0.098 0.022 −0.006 0.014 −0.037 0.3 −0.099 −0.045 −0.116 −0.042 HWE 0.453 0.986 0.708 1 0.858 0.858 0.094 0.363 0.374 Dury N 33 33 33 33 33 33 33 33 32 A 7 5 10 2 8 4 3 9 5 6.222 A~R~ 5.931 4.608 8.451 2 6.828 3.738 3 6.925 4.827 5.145 H~E~ 0.74 0.695 0.817 0.5 00 0.733 0.639 0.633 0.777 0.535 0.674 H~O~ 0.909 0.757 0.787 0.575 0.727 0.696 0.636 0.727 0.593 0.712 F~is~ −0.214 −0.075 0.052 −0.136 0.024 −0.074 0.01 0.08 −0.094 −0.041 HWE 0.31 0.459 0.454 0.489 0.121 0.058 0.987 0.093 0.361 EDar N 21 21 20 21 21 21 16 21 21 A 6 6 11 2 8 4 3 8 6 6 A~R~ 5.699 5.522 9.963 2 7.233 3.946 3 7.471 5.472 5.59 H~E~ 0.732 0.68 0.837 0.495 0.783 0.620 0.646 0.781 0.594 0.685 H~O~ 0.619 0.666 0.85 0.619 0.619 0.571 0.437 0.857 0.666 0.656 F~is~ 0.179 0.044 0.011 −0.226 0.233 0.103 0.352 −0.073 −0.098 −0.098 HWE 0.144 0.822 0.549 0.384 0.002 0.279 0.065 0.945 0.904 EWebB N 25 26 27 28 28 28 27 28 28 A 7 5 13 2 8 4 4 5 6 6 A~R~ 6.142 4.942 10.906 2 6.994 3.809 3.592 4.792 5.103 5.364 H~E~ 0.712 0.686 0.872 0.492 0.686 0.447 0.59 0.689 0.582 0.639 H~O~ 0.72 0.692 0.851 0.571 0.821 0.5 0.629 0.821 0.607 0.69 F~is~ 0.03 0.031 0.061 −0.125 −0.161 −0.082 −0.028 −0.156 −0.005 −0.041 HWE 0.969 0.516 0.265 0.705 0.845 0.332 0.965 0.763 0.632 EWebD N 53 56 57 57 57 52 56 57 52 A 8 5 16 2 9 4 5 10 5 7.111 A~R~ 6.618 4.805 11.322 2 6.829 3.957 3.569 8.182 4.259 5.727 H~E~ 0.769 0.687 0.862 0.49 0.683 0.526 0.605 0.805 0.617 0.671 H~O~ 0.811 0.642 0.877 0.508 0.701 0.634 0.535 0.754 0.634 0.677 F~is~ −0.036 0.083 0 −0.02 −0.008 −0.187 0.132 0.081 −0.007 0.009 HWE 0.553 0.28 0.1 1 0.769 0.51 0.336 0.237 0.078 EWebV N 48 48 49 48 49 48 48 49 47 A 8 5 17 2 9 4 4 11 6 7.333 A~R~ 7.165 4.795 12.381 2 6.752 3.838 3.333 8.405 5.521 6.021 H~E~ 0.809 0.722 0.875 0.477 0.691 0.457 0.603 0.8 0.612 0.672 H~O~ 0.75 0.75 0.918 0.479 0.653 0.458 0.667 0.877 0.489 0.671 F~is~ 0.095 −0.017 −0.028 0.017 0.076 0.02 −0.084 −0.075 0.222 0.023 HWE 0.079 0.476 0.858 1 0.485 0.677 0.209 0.651 0.045 EWebW N 77 77 77 77 77 77 77 77 77 A 7 5 17 2 9 5 4 11 6 7.333 A~R~ 6.245 4.34 11.712 2 6.496 3.608 3.738 8.059 4.227 5.603 H~E~ 0.749 0.688 0.882 0.494 0.668 0.455 0.628 0.77 0.414 0.639 H~O~ 0.853 0.727 0.868 0.467 0.71 0.447 0.608 0.84 0.446 0.663 F~is~ −0.125 −0.044 0.029 0.067 −0.05 0.031 0.046 −0.076 −0.06 −0.024 HWE 0.337 0.649 0.115 0.648 0.097 0.27 0.001 0.13 0.142 Gata N 34 34 34 34 34 32 32 34 34 A 6 4 7 2 7 3 3 5 4 4.556 A~R~ 5.925 3.991 6.185 2 6.579 2.5 3 3.94 2.941 4.118 H~E~ 0.803 0.711 0.805 0.389 0.82 0.494 0.642 0.638 0.517 0.647 H~O~ 0.823 0.764 0.823 0.411 0.764 0.468 0.656 0.647 0.47 0.647 F~is~ −0.01 −0.059 −0.008 −0.043 0.083 0.068 −0.006 0.001 0.106 0.014 HWE 0.036 0.76 0.182 1 0.994 0.572 0.485 0.372 0.866 Har N 35 39 39 40 41 39 26 38 37 A 9 6 19 2 11 4 4 10 7 8 A~R~ 7.81 5.649 13.924 2 7.815 3.635 3.615 8.712 6.364 6.614 H~E~ 0.843 0.798 0.912 0.488 0.775 0.487 0.633 0.845 0.812 0.733 H~O~ 0.8 0.794 0.82 0.45 0.658 0.41 0.615 0.868 0.891 0.701 F~is~ 0.066 0.018 0.114 0.092 0.162 0.171 0.049 −0.014 −0.084 0.057 HWE 0.353 0.552 0.145 0.752 0.351 0.294 0.783 0.394 0.888 Hem N 40 39 31 40 40 40 40 40 40 A 9 5 18 2 11 4 4 9 7 7.667 A~R~ 7.466 4.655 14.027 2 9.235 3.858 3.877 8.033 5.785 6.548 H~E~ 0.824 0.751 0.907 0.474 0.858 0.556 0.674 0.825 0.609 0.72 H~O~ 0.75 0.794 0.935 0.375 0.875 0.575 0.65 0.85 0.6 0.711 F~is~ 0.103 −0.045 −0.014 0.222 −0.006 −0.02 0.048 −0.018 0.028 0.025 HWE 0.281 0.831 0.616 0.185 0.735 0.808 0.371 0.845 0.323 Hol N 26 29 29 29 29 17 24 25 28 A 10 6 13 3 9 4 3 9 6 7 A~R~ 9.109 5.535 10.373 2.552 7.718 3.998 3 8.017 5.806 6.234 H~E~ 0.826 0.775 0.848 0.463 0.717 0.624 0.6 0.752 0.718 0.703 H~O~ 0.807 0.724 0.862 0.482 0.758 0.47 0.541 0.8 0.714 0.684 F~is~ 0.043 0.083 0.002 −0.025 −0.04 0.275 0.119 −0.042 0.024 0.046 HWE 0.353 0.309 0.191 1 0.898 0.08 0.308 0.588 0.735 LChe N 58 59 57 55 58 58 52 59 57 A 8 5 16 2 9 5 4 10 5 7.111 A~R~ 6.95 4.555 10.839 2 6.37 4.155 3.846 8.651 4.677 5.783 H~E~ 0.789 0.625 0.872 0.495 0.745 0.622 0.629 0.851 0.571 0.689 H~O~ 0.741 0.627 0.807 0.472 0.793 0.724 0.73 0.949 0.578 0.713 F~is~ 0.078 0.014 0.093 0.063 −0.047 −0.147 −0.141 −0.098 0.004 −0.018 HWE 0.403 0.686 0.171 0.787 0.488 0.107 0.719 0.364 0.372 RudB N 90 92 94 96 93 92 90 94 92 A 5 5 8 2 3 3 4 6 4 4.444 A~R~ 4.508 4.679 7.681 2 2.994 2.744 3.069 5.137 3.615 4.047 H~E~ 0.677 0.704 0.828 0.496 0.554 0.426 0.524 0.687 0.555 0.606 H~O~ 0.722 0.75 0.787 0.479 0.58 0.326 0.422 0.659 0.543 0.585 F~is~ −0.055 −0.053 0.061 0.045 −0.037 0.245 0.206 0.052 0.033 0.045 HWE 0.334 0.58 0.434 0.686 0.453 0.014 0.021 0.022 0.927 RudC N 35 36 36 36 36 36 35 34 36 A 6 6 9 2 4 3 4 6 4 4.889 A~R~ 5.332 5.262 7.957 2 3.693 2.953 3.825 5.839 3.953 4.535 H~E~ 0.625 0.576 0.832 0.475 0.569 0.519 0.591 0.781 0.664 0.626 H~O~ 0.628 0.556 0.972 0.583 0.583 0.472 0.685 0.852 0.778 0.679 F~is~ 0.025 0.065 −0.14 −0.199 0.003 0.119 −0.131 −0.061 −0.144 −0.056 HWE 0.093 0.172 0.754 0.305 0.11 0.685 0.122 0.578 0.312 RudP N 96 94 94 98 95 92 96 96 95 A 5 5 10 2 3 3 4 8 4 4.889 A~R~ 4.904 4.67 7.256 2 2.817 2.538 3.852 5.251 3.27 4.062 H~E~ 0.706 0.644 0.802 0.462 0.467 0.428 0.595 0.64 0.246 0.554 H~O~ 0.708 0.595 0.787 0.489 0.505 0.445 0.5 0.645 0.242 0.546 F~is~ 0.008 0.086 0.03 −0.049 −0.069 −0.028 0.17 0.003 0.027 0.026 HWE 0.745 0.007 0.106 0.669 0.136 0.768 0.109 0.174 0.097 Swin N 76 80 80 80 80 74 80 80 74 A 9 5 17 2 11 4 5 10 8 7.889 A~R~ 6.327 4.667 11.744 2 7.182 3.858 3.688 9.061 6.225 6.084 H~E~ 0.753 0.707 0.886 0.471 0.786 0.558 0.636 0.849 0.707 0.706 H~O~ 0.802 0.737 0.912 0.425 0.837 0.621 0.7 0.85 0.783 0.741 F~is~ −0.052 −0.03 −0.017 0.111 −0.052 −0.099 −0.088 0.012 −0.094 −0.036 HWE 0.292 0.335 0.428 0.352 0.133 0.594 0.217 0.186 0.445 UChe N 68 70 69 68 67 66 68 64 67 A 7 5 15 2 9 5 4 10 7 7.111 A~R~ 6.01 4.86 11.507 2 7.525 3.921 3.417 8.267 5.35 5.837 H~E~ 0.773 0.684 0.891 0.492 0.796 0.588 0.659 0.814 0.599 0.699 H~O~ 0.735 0.657 0.898 0.441 0.716 0.651 0.691 0.796 0.641 0.692 F~is~ 0.064 0.054 0.007 0.118 0.116 −0.093 −0.033 0.038 −0.056 0.026 HWE 0.765 0.086 0.244 0.462 0.17 0.592 0.735 0.535 0.865 WDar N 114 112 116 119 118 103 112 118 117 A 8 6 15 2 9 5 5 11 7 7.556 A~R~ 5.884 4.62 11.142 2 6.042 3.426 3.286 8.167 4.754 5.48 H~E~ 0.746 0.695 0.89 0.495 0.755 0.544 0.654 0.829 0.579 0.688 H~O~ 0.78 0.687 0.922 0.512 0.779 0.514 0.687 0.813 0.572 0.696 F~is~ −0.036 0.02 −0.027 −0.026 −0.023 0.065 −0.041 0.027 0.021 −0.004 HWE 0.736 0.271 0.939 0.854 0.427 0.703 0.991 0.279 0.099 Web N 32 32 32 31 32 21 29 28 31 A 10 2 12 2 9 4 4 8 6 6.333 A~R~ 8.276 4.994 9.874 2 7.129 3.751 3.551 7.341 5.009 5.769 H~E~ 0.788 0.758 0.871 0.481 0.68 0.447 0.618 0.785 0.53 0.662 H~O~ 0.75 0.781 0.875 0.483 0.656 0.285 0.758 0.785 0.516 0.654 F~is~ 0.064 −0.014 0.011 0.011 0.052 0.383 −0.21 0.017 0.044 0.029 HWE 0.706 0.493 0.474 1 0.029 0.045 0.417 0.11 0.492 WWeb N 122 122 114 125 125 115 120 125 112 A 11 5 18 2 9 4 4 10 7 7.778 A~R~ 7.546 4.732 11.109 2 6.298 3.875 3.58 8.011 4.844 5.777 H~E~ 0.775 0.728 0.88 0.497 0.681 0.544 0.632 0.838 0.595 0.686 H~O~ 0.778 0.721 0.877 0.44 0.728 0.547 0.633 0.864 0.642 0.692 F~is~ 0.005 0.019 0.013 0.124 −0.06 0.002 0.007 −0.022 −0.07 −0.001 HWE 0.276 0.07 0.742 0.221 0.646 0.709 0.191 0.489 0.668 WWebL N 29 24 33 33 33 31 31 31 26 A 8 5 15 2 8 4 3 11 5 6.778 A~R~ 6.675 4.968 11.846 2 6.531 3.76 3 9.709 4.546 5.893 H~E~ 0.763 0.749 0.891 0.477 0.64 0.493 0.608 0.868 0.507 0.666 H~O~ 0.827 0.75 0.939 0.545 0.515 0.387 0.741 0.87 0.461 0.671 F~is~ −0.067 0.02 −0.039 −0.127 0.21 0.231 −0.204 0.014 0.11 0.01 HWE 0.176 0.024 0.337 0.711 0.14 0.155 0.406 0.161 0.176 Mean N 1178 1188 1187 1216 1213 1137 1150 1196 1158 A 13 7 27 3 13 6 5 13 10 A~R~ 6.666 4.798 10.424 2.025 6.54 3.559 3.513 7.39 4.822 H~E~ 0.795 0.734 0.902 0.499 0.741 0.533 0.676 0.836 0.6 H~O~ 0.775 0.705 0.863 0.473 0.707 0.504 0.628 0.802 0.585 n, number of individuals; A, number of alleles; A~R~, allelic richness; H~O~, observed heterozygosity; H~E~, expected heterozygosity; F~is~, inbreeding coefficient (values in bold differ significantly from zero at the 5% level, although none remained significant after table-wide Bonferroni correction); HWE, P-value of the Hardy--Weinberg equilibrium test. Tests for the homogeneity of allele frequency distributions revealed significant genetic differentiation occurred between the majority of the 231 pairwise comparisons, except in nine cases (upper diagonal, [Table 3](#tbl3){ref-type="table"}), of which approximately half involved samples collected from within the same tributary. Quantification of genetic differentiation with F~ST~ values (lower diagonal, [Table 3](#tbl3){ref-type="table"}), demonstrated a range of 0.00--0.16, with a global F~ST~ of 0.04. The highest F~ST~ occurred between samples above significant barriers to fish movement, whereas the lowest, and nonsignificant F~ST~ values, tended to occur between (but not exclusively between) proximate samples from the same or neighbouring tributaries. ###### Tests for genetic differentiation between pairs of samples Amm Ash Dury EDar EWebB EWebD EWebV EWebW Gata Har Hem Hol LChe RudB RudC RudP Swin UChe WDar Web WWeb WWebL ------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ---------- ---------- ------------ Amm -- *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ NS ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* Ash 0.050 -- ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* **^\^* Dury 0.021 0.091 -- ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* EDar 0.016 0.068 0.021 -- *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* EWebB 0.023 0.085 0.017 0.023 -- *^\^ NS NS ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* NS *^\^ ^\^* EWebD 0.025 0.068 0.021 0.016 0.005 -- NS *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* NS *^\^ ^\^* EWebV 0.021 0.054 0.020 0.013 0.007 0.007 -- *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* NS *^\^ ^\^* EWebW 0.023 0.077 0.012 0.021 0.000 0.004 0.004 -- *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* Gata 0.050 0.067 0.086 0.073 0.087 0.079 0.058 0.076 -- *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ Har 0.013 0.068 0.042 0.040 0.040 0.032 0.028 0.045 0.079 -- ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ Hem 0.000 0.041 0.021 0.020 0.020 0.018 0.018 0.017 0.031 0.011 -- ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* Hol 0.014 0.050 0.028 0.016 0.029 0.019 0.005 0.020 0.053 0.018 0.007 -- *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* LChe 0.019 0.077 0.013 0.007 0.024 0.019 0.020 0.019 0.077 0.043 0.023 0.026 -- *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ RudB 0.076 0.119 0.056 0.072 0.039 0.045 0.046 0.044 0.140 0.073 0.071 0.067 0.054 -- ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ RudC 0.068 0.122 0.056 0.061 0.026 0.027 0.045 0.031 0.129 0.067 0.066 0.065 0.048 0.021 -- ^\^* *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* RudP 0.092 0.153 0.053 0.095 0.059 0.078 0.064 0.053 0.160 0.112 0.090 0.090 0.071 0.033 0.061 -- *^\^ ^\^* *^\^ ^\^* *^\^ ^\^* Swin 0.016 0.079 0.015 0.013 0.024 0.021 0.026 0.029 0.083 0.027 0.018 0.029 0.011 0.060 0.050 0.090 -- *^\^ ^\^* *^\^ ^\^* *^\^ UChe 0.016 0.081 0.012 0.008 0.020 0.017 0.021 0.019 0.072 0.036 0.013 0.027 0.000 0.050 0.044 0.071 0.006 -- ^\^* *^\^ ^\^* *^\^ WDar 0.021 0.065 0.024 0.013 0.034 0.031 0.023 0.034 0.075 0.041 0.018 0.026 0.009 0.063 0.076 0.088 0.014 0.011 -- ^\^* *^\^ ^\^* Web 0.029 0.091 0.013 0.023 0.000 0.000 0.008 0.002 0.086 0.036 0.017 0.022 0.020 0.025 0.018 0.050 0.021 0.014 0.030 -- *^\^ NS WWeb 0.021 0.077 0.013 0.033 0.011 0.012 0.012 0.011 0.081 0.023 0.019 0.024 0.029 0.040 0.039 0.060 0.025 0.025 0.034 0.005 -- NS WWebL 0.021 0.099 0.013 0.026 0.015 0.009 0.010 0.013 0.086 0.027 0.016 0.025 0.024 0.037 0.034 0.063 0.013 0.016 0.025 0.000 0.000 --** The upper diagonal shows pairwise F~ST~ values; all significant values (P \< 0.05) are highlighted in bold. The lower diagonal shows the result of tests for homogeneity of allele frequencies: NS, not significant; ^\^significant at the 5% level. Table-wide significance levels were applied using the sequential Bonferroni procedure (k* = 231) for all tests. The NJ D~CE~ phylogram ([Fig. 2](#fig02){ref-type="fig"}) reveals several samples that have high bootstrap support and relatively long branch lengths, namely the Rud group of samples and the Gata and Ash; this relates well to their positions above significant barriers to fish movement ([Fig. 1](#fig01){ref-type="fig"}) that may have acted to isolate these samples from the rest of the catchment. Moderate support is also noted on the phylogram among groups of samples from the upper west (Che, WDar, Swin, Dury and EDar), upper east (Web, EWeb and WWeb) and lower (Amm, Har, Hol and Hem) areas of the catchment. In addition, there is some support for proximate groups of samples, especially those collected within the same tributary, e.g. within the West and the East Webburn. A principal component analysis (PCA) was also performed on these data using the default settings in [genalex]{.smallcaps} 6 ([@b50]), the findings of which support the main conclusions of the phylogram; the PCA plot in [Fig. S1](#SD1){ref-type="supplementary-material"}. ![Neighbour-joining phylogram based on pairwise D~CE~ distances between samples. Numbers next to branch nodes represent bootstrap support (%) based on 1000 replicates, only values over 50% are shown. Sample abbreviations match [Table 1](#tbl1){ref-type="table"}.](eva0002-0537-f2){#fig02} Decomposed pairwise regression ------------------------------ Genetic distance was positively correlated with geographic distance when comparing all pairwise sample combinations, but the correlation was weak and nonsignificant (P = 0.137, r^2^ = 0.036; [Fig. 3](#fig03){ref-type="fig"}). Based on the systematic bias of the regression residuals (process one) nine putative outlier samples were detected; RudP, Ash, Gata, RudB, RudC, Hem, Amm, WDar and UChe. The AIC values were compared for models with and without putative outliers (process two) and the best model included 17 samples (indicating RudP, Ash, Gata, RudB and RudC were true outliers; [Table 4](#tbl4){ref-type="table"}). This result is consistent with a priori predictions as all these samples originated from sites above significant barriers to fish movement. The exclusion of these samples strengthened the positive correlation between genetic and geographic distance, which also become statistically significant (P \< 0.001, r^2^ = 0.476; [Fig. 3](#fig03){ref-type="fig"}). Each of the outlier samples was individually regressed with the nonoutlier samples, which indicated that the majority of outlier samples were significantly diverged from adjacent populations but exhibited strong and significant correlations between genetic and geographic distance ([Fig. 4](#fig04){ref-type="fig"}). This suggests that despite of a strong effect of genetic drift acting on the isolated samples (either through small effective population size or founder effects or bottleneck) evidence of gene-flow still remains. The Ash sample was the exception; while significantly divergent from the other samples, it showed no correlation between genetic and geographic distance, suggesting that the effect of genetic drift far outweighs that of gene flow. The decomposed regressions of the 17 nonoutlier samples showed similar regression lines with significant relationships between genetic and geographic distance, except for the Amm, Hol and Swin ([Fig. 4](#fig04){ref-type="fig"}). This suggests that these samples are close to, or at, equilibrium between drift and gene flow. ![Relationship between genetic distance \[F~ST~/(1 − F~ST~)\] and geographic distance (km) for all 22 samples (open and closed diamonds combined; r~xy~ = 0.191, P = 0.137, r^2^ = 0.036, upper line) and excluding the five outlier samples (filled diamonds only; r~xy~ = 0.690, P \< 0.001, r^2^ = 0.476, lower line).](eva0002-0537-f3){#fig03} ###### Fit of alternative models with and without the putative outlier samples Samples excluded n k r^2^ P value AIC~C~ ΔAIC~C~ --------------------------------------------------- ----- ----- ---------- ----------- --------- --------- RudP, Ash, Gata, RudB, RudC 17 1 0.4768 \<0.001 −108.49 0.00 RudP, Ash, Gata, RudB, RudC, Hem 16 1 0.5281 \<0.001 −103.26 5.23 RudP, Ash, Gata, RudB, RudC, Hem, Amm 15 1 0.6292 \<0.001 −99.37 9.12 RudP, Ash, Gata, RudB, RudC, Hem, Amm, WDar 14 1 0.6504 \<0.001 −94.50 13.98 RudP, Ash, Gata, RudB 18 1 0.1353 0.064 −90.73 17.76 RudP, Ash, Gata, RudB, RudC, Hem, Amm, WDar, UChe 13 1 0.6459 \<0.001 −87.68 20.81 RudP, Ash, Gata 19 1 0.0612 0.1099 −86.11 22.38 RudP, Ash 20 1 0.0880 0.066 −75.52 32.97 RudP 21 1 0.0589 0.076 −72.33 36.16 None 22 1 0.0335 0.142 −68.86 39.63 n refers to the number of samples and k the number of parameters. ![Decomposed pairwise regression of genetic distance \[F~ST~/(1 − F~ST~)\] and geographic (km) distances for the 22 samples. Each of the five outlier samples was regressed with the 17 nonoutlier samples, whilst each of the 15 nonoutliers was regressed with the other 14 samples. Solid and dashed lines represent statistically significant or nonsignificant regressions respectively.](eva0002-0537-f4){#fig04} Spatial autocorrelation ----------------------- Tests of microspatial autocorrelation at the level of the individual were carried out on samples not isolated above barriers to fish movement (this included all 17 samples not identified in the DPR as true outliers). The results showed that the genetic autocorrelation coefficient (r) was significantly positive at the 0--5 and 5--15 km size classes, and intercepted the x-axis at 20 km ([Fig. 5A](#fig05){ref-type="fig"}); results from the analysis of alternative classes produced broadly similar results, with intercepts ranging from 15 to 20 km (results not shown). In all size classes above 15 km, r was significantly negative, meaning that proximal individuals showed greater genetic divergence than that expected for a random distribution of genotypes, although in the largest size classes r approached the null hypothesis of no significant structure. The MDC analysis with increasing distance size classes revealed that r was significantly positive for distance classes up to and including 25 km ([Fig. 5B](#fig05){ref-type="fig"}). The inclusion of specimens separated by \>45 km meant that significant positive genetic autocorrelation was no longer observed. The addition of samples collected above barriers did not radically alter the results of the spatial autocorrelation (analysis not shown), except in the correlogram ([Fig. 5A](#fig05){ref-type="fig"}), in which case r was not as strongly negative (r = −0.015 in the 25 km class) and at the largest distance class the null hypothesis could not be rejected. However, because of the uncertainties of applying an individual-based test to samples collected at specific sample sites (where separation between individuals is assumed to be zero), these findings should be interpreted with some caution. ![Spatial autocorrelation analyses with samples isolated above barriers removed. (A) correlogram of the genetic correlation (r) as a function of distance. (B) The genetic correlation (r) as a function of increasing distance classes. Dotted lines (A) and grey bars (B) indicate the 95% confidence interval (CI) about the null hypothesis and error bars about r indicate the 95% CI.](eva0002-0537-f5){#fig05} Discussion ========== The purpose of this study was to examine, within-catchment population structure of brown trout in a region that despite being a focus for salmonid fishing and conservation, has until now, received relatively little attention. The results revealed significant differentiation among samples collected within a single river catchment and, in the case of the Ruddycleave and Cherry Brook, even between sample sites within a tributary. These results demonstrate that Dart trout do not represent a single panmictic population in which gene flow is unrestricted across the catchment. The global F~ST~ across all 22 samples sites was 0.04, with a range of 0.000--0.160 for pairwise F~ST~ estimates, which accords with previous work on brown trout employing microsatellites (e.g. [@b9], F~ST~ = 0.00--0.114; [@b35], 0.009--0.065; [@b31], 0.010--0.071; [@b47], 0.004--0.154). Effect of barriers ------------------ What is particularly striking from the phylogram ([Fig. 2](#fig02){ref-type="fig"}) and pairwise F~ST~ estimates ([Table 3](#tbl3){ref-type="table"}) is the effect barriers have on population structure; the largest values all occur between comparisons involving samples isolated above a barrier to fish movement. The significant effect of barriers on population structure has been previously documented and has been associated with reductions in population size, bottlenecks and genetic drift ([@b33]; [@b42]; [@b49]; [@b73]). Such processes may also have been in operation in these isolated samples identified within the River Dart, as the levels of heterozygosity and allelic richness were also depressed ([@b11]). The results of the DPR analysis also afford some further insight into the demographic processes occurring within these samples. In the case of the Ash sample, genetic drift has acted to obscure any correlation between genetic and geographic distance between samples; as the barrier to migration on this tributary is man-made (and therefore not ancient), small effective population size and founder effects appear to be the most likely explanation for the patterns of genetic divergence observed. In the case of the other highly diverged and isolated samples (RudC, RudB, RudP and Gata) a relatively strong correlation between genetic and geographic distance remains, suggesting that effective population sizes have not been reduced to the level that genetic drift is strong enough to obscure the correlation. Alternatively, some form of gene flow could be occurring, perhaps associated with barriers being by-passed in high flows. However, it is interesting to postulate that unidirectional, downstream migration from the isolated areas could act to partially restore the correlation between genetic and geographic distance. The importance of identifying barriers to fish movement has been highlighted for a number of conservation issues, in particular, the negative effects of genetic drift in small populations and the isolation of indigenous stocks from the effects of stocking undertaken below barriers ([@b79]; [@b73]), both topics that appear to warrant further investigation within the River Dart. Population structure and evolutionary models -------------------------------------------- The phylogram ([Fig. 2](#fig02){ref-type="fig"}) shows that genetic structuring among samples within the catchment is present; moderate levels of bootstrap support occurred between three groups of proximate samples from the upper east, upper west and lower Dart. This association between genetic and geographic distance is further supported by a significant effect of isolation-by-distance, as demonstrated by DPR analysis ([Fig. 4](#fig04){ref-type="fig"}). However, a strongly negative genetic correlation (r) was identified at the 25 and 45 km size classes used in the spatial autocorrelation on Dart trout ([Fig. 5A](#fig05){ref-type="fig"}), meaning that proximal individuals showed greater genetic divergence than that expected for a random distribution of genotypes. Such a finding may be the result of a discontinuity in gene flow between trout in different tributaries or could reflect the fact that some sampling was completed outside of the spawning season, and therefore, may include adult specimens of trout that may have moved away from nursery areas. The observation of isolation-by-distance at the intra-catchment level is somewhat at odds with many of previous studies describing the population structure of brown trout ([@b12]; [@b22]; [@b43]; [@b4]; [@b61]), although, it is not unique ([@b19]; [@b8]). Recent studies of anadromous brown trout inhabiting relatively small rivers in Denmark and the Baltic Sea ([@b39]; [@b47]; [@b35]) suggested a population structure consisting of a system of highly interconnected, small and unstable populations where, in accordance with the metapopulation model, there was no significant effect of isolation-by-distance and a lack of temporal stability (even over the short-term). This pattern was generally linked to high levels of gene flow and occasional extinction--recolonization events caused by environmental instability, e.g. low summer water levels ([@b47]). These results sharply contrast with the population structure described in this study, where a significant effect of isolation-by-distance (once outliers have been excluded) and at least short-term temporal stability of population structure was observed. Therefore, it appears that, despite the potential for low pH to perturb the environment, the population structure of brown trout inhabiting the tributaries of the River Dart is determined more by ecological events and natal homing, than by rare stochastic extinction events, with migration occurring mostly between neighbouring groups. The key to reconciling these contrasting results among studies appears to be catchment size, whereby larger population systems appear to be stable and smaller systems tend to undergo localized extinction--recolonization events ([@b31]; [@b47]; [@b35]; [@b44]; [@b55]). Historical and temporal effects ------------------------------- There are some limitations to this study; in particular, the effects of postglacial recolonization and stocking on population structure of Dart trout still await assessment. Although, the results of the DPR analysis suggests the majority of the samples are at, or close to, drift--migration equilibrium following such perturbation ([Fig. 4](#fig04){ref-type="fig"}). In particular, these processes (especially artificial stocking), would generally have acted to obscure the strong pattern of isolation-by-distance identified in this study ([@b38]; [@b45]), suggesting they are not the strongest determinants of population structure in this case. In addition, the temporal samples collected in the study represent only a subset of sites from across the catchment and cover a relatively short period: 2002--2004. [@b49] found that the probability of detecting significant allele frequency differences between temporal samples taken from the same population, but spaced only a few years apart, could be small. Indeed, if extinction events happen infrequently, i.e. over the scale of decades, then this instability may not become evident in samples taken only a few years apart (although the strong pattern of isolation-by-distance identified suggests longer term temporal stability, at least as long as it takes for drift--migration equilibrium to be established after perturbation). Evolutionary hypotheses ----------------------- The hypotheses proposed by [@b24] provide a useful framework within which to analyse population structure; however, they remain quite general and any situation in which gene flow is limited by geographic distance may yield similar results. Indeed, work on genetic population structure of Dolly Varden charr (Salvelinus malma; [@b37]) yielded analogous results to the present study, but the authors suggested that a source-sink metapopulation structure best fitted their results. In that case, outlier samples were identified in the absence of barriers to migration, suggesting founder effects or bottlenecks had occurred; such factors have not been identified within the current study of the River Dart (where the results of the DPR actually suggest relatively stable population structure). Additionally, many of the predictions of the proposed models are quite simplistic, e.g. the prediction that that there would be no significant pattern of isolation by distance in a metapopulation may not hold true if recolonization and gene flow occurred predominantly between neighbouring populations (a scenario made more likely by the linear nature of a river). Another prediction, that the level of genetic structuring would be expected to be lower under a metapopulation model, can also be questioned. It has been shown that the range of F~ST~ estimates in this study is similar to that used previously to describe both small temporally unstable populations ([@b35]) and large stable populations ([@b31]). It appears that levels of differentiation, especially F~ST~ values, may not differ under the two evolutionary models summarized by [@b24] and are dependant on the complex mechanics of recolonization ([@b32]; [@b44]). Indeed, extinction--recolonization events may act to increase levels of genetic differentiation ([@b28]; [@b27]). Delineating demographic units ----------------------------- Spatial autocorrelation analyses were used to determine the geographic scale of genetic structuring within the River Dart. [Figure 4B](#fig04){ref-type="fig"} illustrates the tendency for genetic distance between individuals to decrease with increasing distance, such that at in-water distances of \>45 km gene flow is minimal. It has also been proposed that the x-axis intercept of the correlogram ([Fig. 5A](#fig05){ref-type="fig"}) be considered as a minimum distance that can conserve genetic diversity at a lower cost ([@b13]), resulting in a management unit size of approximately 15--20 km for the River Dart. The results from spatial autocorrelation analyses bear some similarities to work on Atlantic salmon in the Varzuga River in Russia ([@b55]), which also highlighted the importance of conserving multiple spawning and nursery areas for the long-term preservation of fish populations. However, most striking difference is the distance across which gene flow was observed within the Varzuga; the genetic correlation remained positive at distances up to 120 km and the x-axis intercept of the correlogram occurred at 34 km. This may reflect the larger size of the Varzuga River (when compared with the River Dart), and the fact that samples were separated by greater average in-water distances ([@b74]). Alternatively, it is interesting to hypothesize that the lower distance over which gene flow occurs in brown trout may reflect their resident life history, resulting in more restricted gene flow and greater genetic differentiation ([@b29]; [@b36]; [@b44]). Conclusions =========== Brown trout inhabiting the River Dart demonstrate significant within-river population differentiation; this differentiation is most significant when associated with barriers to movement, but otherwise demonstrates a pattern of isolation-by-distance and at least short-term temporal stability. These results are taken as evidence that ecological events are more important in shaping the population structure of Dart trout than stochastic extinction events, and certainly do not contradict the expectations of a member-vagrant evolutionary model of population structure for Dart trout ([@b24]). However, the results of the spatial autocorrelation demonstrate gene flow does occur between neighbouring samples, suggesting the need to conserve not only different spawning areas within the basin (particularly in different tributaries), but links between them as well. This research was supported by funding from the Natural Environment Research Council (NERC), UK through the award of a CASE studentship (NER/S/A/2001/06178) with the Westcountry Rivers Trust (CASE partner) and the award of a NERC training grant to work at the Sheffield Molecular Genetics Facility (SMGF/047). The EA is acknowledged for assistance in sample collection, in particular Fisheries Officers Dave Hoskin and Adam Bailey, without whom the project would not have been possible. Further acknowledgement is also due to all those who helped with fieldwork, especially Jan Shears and Phil Shears, and to Anna Finnegan for provision of stocking data and GIS support. This study also benefited from technical training by members of the Sheffield Molecular Genetics Facility: Terry Burke, Deborah Dawson and Andy Krupa. Supporting Information ====================== Additional Supporting Information may be found in the online version of this article: Figure S1. Principal componentanalysis plotted from a matrix of pairwise Nei\'s geneticdistances between all populations and computed using the programgenalex (Peakall andSmouse 2006). Axis 1 explains 36% of the variation and axis 2, 22%of the variation. Populations analysed are the same as thoseanalysed in the phylogram ([Fig. 2](#fig02){ref-type="fig"}); sample abbreviationsmatch [Table 1](#tbl1){ref-type="table"}. Please note: Wiley-Blackwell are not responsible for the content or functionality of any supporting materials supplied by the authors. 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Introduction ============ Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous in the environment and cause adverse environmental effects. The exploration and exploitation of crude oil and gas resources are a major source of PAHs. Even though improved technologies have been introduced in the petroleum industry, accidents continue to occur, resulting in hydrocarbon pollution of the environment (both land and water) in most oil producing countries, including Nigeria.[@i2156-9614-9-24-191204-b1] Oil from the petroleum industry enters the aquatic environment through gas flaring, disposal of used lubrication oils, washings from oil tanks, leakage from marine vessels, erosion and run off from crude oil polluted lands, refinery effluents, and ruptures from poorly maintained flow lines/installations. Leakage of oil into the environment could be due to sabotage or maintenance and engineering errors. Upon entry into the aquatic environment, the fraction either mixes with water or sinks into the sediment, causing severe damage to benthic organisms. Hydrocarbon pollution impacts fish, crustaceans and mollusks with objectionable odor or flavor, reducing their market value and acceptability.[@i2156-9614-9-24-191204-b1] Major routes of PAH exposure in fish are ingestion of contaminated food and diffusion of water across their gills and skin.[@i2156-9614-9-24-191204-b2] The lipophilic nature and high chemical stability of PAHs make it easier to penetrate biological membranes and accumulate in the fatty tissues of organisms following their uptake. Polycyclic aromatic hydrocarbons have been reported to be readily absorbed by fish and other aquatic organisms on exposure to contaminated materials, thereby reaching elevated levels over that of the surrounding medium.[@i2156-9614-9-24-191204-b2] The bioaccumulation pattern of PAHs vary in aquatic organisms depending on the trophic levels they occupy, however, the organic PAHs physiological burden is dependent on the biotransformative effect of the organisms.[@i2156-9614-9-24-191204-b3] Macrobenthic invertebrates (shrimps, crayfish, mollusks and crabs) are an important and integral part of the aquatic ecosystem and thus reflect any negative effects caused by pollution in the community structure which can affect trophic relationships.[@i2156-9614-9-24-191204-b4] Fish have been reported to be the most sensitive living organism to trace concentrations of toxicants in aquatic habitats.[@i2156-9614-9-24-191204-b5] Shrimps, crabs and fishes are therefore good indicators of pollution in coastal waters and have been used extensively for environmental monitoring.[@i2156-9614-9-24-191204-b6] Polycyclic aromatic hydrocarbons are classified into two main groups, low and high molecular weights, based on their physical and biological properties and number of fused aromatic rings contained in their structure. Light or low molecular weight (LMW) PAHs consist of 2--3 aromatic rings, and heavy or high molecular weight (HMW) PAHs consist of 4--6 rings.[@i2156-9614-9-24-191204-b7],[@i2156-9614-9-24-191204-b8] The HMW PAHs are more persistent and recalcitrant (less readily bio-degraded by indigenous microorganisms) than LMW PAHs and can persist in an aqueous environment and bioaccumulate in aquatic organisms like fish and shrimps, and are more carcinogenic.[@i2156-9614-9-24-191204-b9] The LMW PAHs, although less carcinogenic, also pose toxic risks to many aquatic organisms.[@i2156-9614-9-24-191204-b10] The stability and distribution of PAHs in the natural environment is influenced by the chemical structure, chemical configuration and physical and chemical properties of the aromatic rings.[@i2156-9614-9-24-191204-b8],[@i2156-9614-9-24-191204-b11] The spectrum of PAHs in the water ecosystem, including water, fish, and sediment can provide some information about their emission source. Higher concentrations of LMW PAHs (e.g., acenaphthene, fluorene) are usually related to naturally occurring PAHs, either of petrogenic or pyrogenic origin, while PAHs emitted from combustion processes (pyrolytic origin) often contain elevated concentrations of HMW (e.g., phenanthrene, fluoranthene, pyrene) and fewer LMW PAHs.[@i2156-9614-9-24-191204-b11] Polycyclic aromatic hydrocarbons have received attention due to their potential negative effects on human and ecosystem health. Adverse effects of PAHs have also been observed in marine organisms, which include impairment in growth and development, growth reduction, endocrine alteration, malformations of embryo and larvae and DNA damage.[@i2156-9614-9-24-191204-b12] ERL : Effect range low ERM : Effect range median HMW : High molecular weight LMW : Low molecular weight SV : Screening value TEF : Toxicity equivalency factor TEQ : Toxic equivalent quotient USEPA : United States Environmental Protection Agency Aquatic foods are high in nutritive value and thus highly desirable due to their contribution of high-quality protein and low fat content. This attracts consumers to these foods due to their health benefits in addition to their widespread availability and relatively low price, although exposures to toxic chemicals have been a concerning issue for years. In Nigerian markets, fish are one of the most common aquatic organisms available for consumption and reportedly provide over 60% of protein intake.[@i2156-9614-9-24-191204-b15] Food consumption has been identified as an important pathway of human exposure to many contaminants, including PAHs. Therefore, PAH contamination of widely consumed fish species among the populace may have serious health implications as some of these aquatic organisms are caught in water polluted by hydrocarbons.[@i2156-9614-9-24-191204-b16] The objectives of the present study are to determine the concentration of PAHs in sediment samples and in two commercially important fish species, Drepane africana and Pomadasys jubelini, crabs, and shrimps around the Atlas Cove jetty. Additionally, the present study aims to assess the health risk associated with the consumption of fish species and shellfish in the study area. Methods ======= The study was carried out around the Atlas Cove jetty ([Figure 1](#i2156-9614-9-24-191204-f01){ref-type="fig"}), which is an offloading and storage depot for imported refined oil prior to distribution to other depots. Oil spillage has been reported in the process of operations in Commodore channel. The channel is approximately 10 m deep at the entrance, 12--15 m deep inward, 0.5 - 1 km wide, and 10 km long. It is tidal, and water from the Atlantic Ocean moves in during high tides and recedes during low tides. Turbulence is very high due to its proximity to the Atlantic Ocean. In addition to oil-related activities that go on around the jetty, it is well known for the movement of shipping vessels along the waterways. ![Map of the study area showing sampling points](i2156-9614-9-24-191204-f01){#i2156-9614-9-24-191204-f01} The jetty is located in Lagos State between latitudes 6°21′ N to 6°34′ N and longitudes 3°01′ E to 3°27′ E in the southwestern region of Nigeria. The water around Atlas Cove jetty is brackish (mixture of fresh and marine water). The lagoon plays an important role for the human community due to the large prosperous molluscan and fishing exploitation and commerce. It is also used for artisanal fishing, as a large part of the domestic fish supply in Nigeria comes from inland waters, such as lagoons, and thus provides a means of livelihood for fishermen. However, this industry is being threatened by concentrations of PAHs in this area. Sample collection ----------------- A total of 45 surface sediment samples were collected in five different locations, at 5 cm depth, around Atlas Cove jetty between June to August 2016. Sediment samples were collected from five different sites, all of which were impacted by anthropogenic activities such as ship traffic and offloading. Sediment samples were collected using sediment grab and transferred onto aluminum foil papers. Twelve (12) samples of each fish species and 20 samples of shrimps and crabs were purchased from local fishermen at the landing site of the study area and transported to the laboratory on ice packs. Upon arrival at the laboratory, the samples were removed from the ice, thawed, and cleaned under running tap water to remove any dirt and then rinsed again with distilled water. The shrimp, crab and fish samples were taxonomically identified using standard reference sources by experts at the Department of Zoology of Obafemi Awolowo University, Ile-Ife Nigeria. Samples were stored separately at −20°C in a freezer. Sample identification --------------------- Two species of fishes were identified as Pomadasys jubelini, (common name: grunter) ([Figure 2](#i2156-9614-9-24-191204-f02){ref-type="fig"}) and Drepane africana, (local name: akaraba) ([Figure 3](#i2156-9614-9-24-191204-f03){ref-type="fig"}). The crab was identified to be the male species of Callinectes amnicola, (common name: marine blue crab) ([Figure 4](#i2156-9614-9-24-191204-f04){ref-type="fig"}), the shrimp was identified as Penaeus notialis, (common name: pink shrimp) ([Figure 5](#i2156-9614-9-24-191204-f05){ref-type="fig"}). The sampled fish, shrimp, and crab were identified as either demersal, benthopelagic or pelagic species. ![Pomadasys jubelini (grunter) sample from Atlas Cove](i2156-9614-9-24-191204-f02){#i2156-9614-9-24-191204-f02} ![Drepane africana (spadefish) sample from Atlas Cove](i2156-9614-9-24-191204-f03){#i2156-9614-9-24-191204-f03} ![Callinectes amnicola (blue marine crab) sample from Atlas Cove](i2156-9614-9-24-191204-f04){#i2156-9614-9-24-191204-f04} ![Penaeus notialis (pink shrimp) sample from Atlas Cove](i2156-9614-9-24-191204-f05){#i2156-9614-9-24-191204-f05} ### Ecology and habitat of Pomadasys jubelini and Drepane Africana Pomadasys jubelini is found in sandy and muddy bottoms in coastal waters and estuaries and occurs in freshwater and brackish waters. It feeds on fish, small crustaceans, and mollusks.[@i2156-9614-9-24-191204-b17] It is a bottom-living, but periodically pelagic species usually inhabiting littoral waters to about 25 m depth, but has been reported to extend down to about 90 m. It is locally abundant in shallow waters throughout its range. Drepane africana is a neritic, coastal species and occurs in lagoon and estuarine habitats over sandy and muddy substrata between 20 and 50 cm depth. It feeds on fish eggs, benthic invertebrates, and detritus.[@i2156-9614-9-24-191204-b18] ### Ecology and habitat of Callinectes amnicola and Penaeus notialis Callinectes amnicola (blue marine crab) is a genus of crab from the family Portunidae usually found in the lagoon. The crabs may be considered as euryphagous, feeding on fishes, mollusks, crustaceans, higher plant materials, algae and diatoms. It is found in sand and ocean bottoms.[@i2156-9614-9-24-191204-b19] Penaeus notialis (pink shrimp) is a species of shrimp known to feed on diatoms, green algae, plants materials, as well as crustaceans and fish fragments. It spends a part of its life cycle in open water (ocean), but is mostly found in estuaries, lagoons, open sea and creeks. Its primary habitat (especially adults) is sand, sand- shell or coral- mud bottoms from intertidals.[@i2156-9614-9-24-191204-b20] Sample pre-treatment -------------------- Sediment samples were air dried for several days, after which stones and debris were removed from the samples and then pulverized and passed through a 2-mm mesh sieve to remove other unwanted materials. Samples for PAH analyses were further sieved through 0.5-mm mesh sieve and stored in foil papers until extraction was performed. The fish samples were allowed to thaw, the scales were removed and washed with running water and then distilled water before dissecting and removing the flesh and other parts which were put in sample bottles. Samples included fillets containing only fleshy parts and whole fish, including bone, fleshy parts and organs. The fish samples were weighed using an analytical weighing balance (wet weight) and homogenized with anhydrous sodium sulphate in a mortar with pestle. The mixture was labeled and wrapped in aluminum foil. It was left till the next day to cake, prior to extraction. Reference standards ------------------- Standard mix solutions of the United State Environmental Protection Agency\'s (USEPA) 16 priority PAHs, each at 100 μg/L in dichloromethane, were purchased from Sigma-Aldrich (St. Louis, MO, USA). The surrogate standard was a mixture containing naphthalene-d~8~ (N-d~8~), acenaphthene-d~10~ (Ace-d~10~), phenanthrene-d~10~ (Phen-d~10~), chrysene-d~12~ (Ch-d~12~) and perylene-d~12~ (Per-d~12~), which was added to the samples before extraction and used as internal standards for quantification. Stock solutions were used to prepare working standard solutions for calibration and spiking experiments. Extraction procedure for PAHs in sediment and aquatic organisms --------------------------------------------------------------- Polycyclic aromatic hydrocarbons in sediment samples were extracted using a Soxhlet extraction according to the method described by the Association of Official Analytical Chemists.[@i2156-9614-9-24-191204-b21] Five (5) g of each sediment sample was weighed and 5 g of anhydrous sodium sulphate was added to each sample. The samples were placed in a cellulose thimble and extracted for 16 to 24 hours using 150 ml of dichloromethane in a Soxhlet extractor. The extract was concentrated by evaporation overnight in a fume cupboard and covered with a perforated aluminum foil. Polycyclic aromatic hydrocarbons in the biota samples were determined according to the method of USEPA 3540C.[@i2156-9614-9-24-191204-b22] A total of 5 g of each species of shrimp, crab and fish samples that had been previously homogenized with anhydrous sodium sulfate were poured into 100 ml beakers and 40 ml of n-hexane and dichloromethane (1:1 vol/vol) was used as an extracting solvent. The beaker with the content was placed on a magnetic stirrer and shaken for about 25 minutes. The extract was decanted into a clean conical flask, then 20 ml of fresh solvent was added, and the process repeated. The extracts were combined and filtered through a small glass funnel containing a layer of anhydrous sodium sulphate over a plug of glass wool into a receiving conical flask. The extracts were concentrated by allowing to stand overnight in a fume cupboard and covered with perforated aluminum foil. Sample clean-up was carried out for both sediment and biota using USEPA Method 3630C.[@i2156-9614-9-24-191204-b23] A 600 × 19 mm clean up column was prepared. The hole was blocked with glass wool, 3 g of activated silica gel (60 mesh) was added and the column was topped with sodium sulfate. The column was rinsed by eluting with 20 ml n-hexane and discarded. The concentrated extract was loaded onto the prepared column and eluted with 50 ml n-hexane. The eluates were then concentrated to 1 ml using a rotary evaporator under a gentle stream of pure nitrogen. One (1) ml of the extract was then transferred into a well labeled vial and stored at 4°C prior to gas chromatograph mass spectrometry analysis. Instrumental and analytical conditions -------------------------------------- Analyses of PAHs were performed for both sediment and biota samples using a gas chromatograph mass spectrometer with selected ion monitoring (Shimadzu QP 2010 gas chromatograph mass spectrometry equipped with AOC 5000 auto injector). The column used was a Varian Factor Four fused silica capillary column (30 m × 0.25 mm × 0.25 μm film thickness) for separating target analytes. Helium was used as the carrier gas at a flow rate of 1.2 mL/min. The sample injector temperature was set at 250°C and 300°C and samples were injected at a volume of 1 mL in splitless mode. An initial column temperature of 60°C was held for 1 min and ramped from 60°C to 200°C at 10°C/min held for 2 min and finally to 300°C at 10°C/min and held for 6 min. The mass spectrometry conditions were set as follows: ionization source: electron ionization at -- 70 eV: ion source temperature: 200°C: store mass range m/z 47 - 400 μm. Identification of the individual PAHs was based on comparison of retention time between samples and standard solutions. Quality control --------------- The blanks were treated the same way as the samples. Sediment and biota samples were spiked. These fortified matrices were used as calibration standards, and the range of concentrations added to both sediment and biota matrices were used to produce the calibration curves of 20 - 100 mgkg^−1^. The surrogate internal standards were added to the spiked sediment and biota samples at 100 mgkg^−1^. The response factors were then calculated using the response obtained from desorption of a standard solution containing 40 mgkg^−1^ of the 16 PAHs of interest and 100 mgkg^−1^ of each internal standard. Spiked samples were extracted and analyzed. Recovery yields were 75 - 110% and limit of detection for individual PAHs ranged from 0.02 to 30.00 mgkg^−1^ in sediment and biota with a signal to noise ratio of three (3) and limit of quantization of signal to noise ratio of ten (10). Human health risk assessment ---------------------------- Toxicological risks associated with PAH concentrations in the biota samples were assessed through comparison of the observed concentrations with regulatory limits and guidelines. ### Potential human health risk To assess human health risks from exposure to PAHs through consumption of possibly contaminated biota samples (dietary intake), the dietary daily intake concentrations of PAH\'s from consumption of contaminated shrimps, crabs and fish species were determined. The dietary daily intake of PAHs in contaminated biota samples were assessed for the adult population using [Equations 1](#i2156-9614-9-24-191204-e01){ref-type="disp-formula"}, [2](#i2156-9614-9-24-191204-e02){ref-type="disp-formula"} and [3](#i2156-9614-9-24-191204-e03){ref-type="disp-formula"}. The daily intake of PAHs from the biota samples was calculated by multiplying the respective PAH concentration in each sample by the consumption rate of an average weight adult (70 kg). where, 0.0685 kg/day is based on the assumption that an average Nigerian consumes 25 kg of fish per annum and an average of 0.0016 and 0.0219 kg/day of crabs and shrimp, respectively.[@i2156-9614-9-24-191204-b5],[@i2156-9614-9-24-191204-b15] ### Carcinogenic risk assessment of polycyclic aromatic hydrocarbons in biota samples Cancer risk due to dietary exposure to PAHs in fish was assessed. The carcinogenic potencies of individual PAHs were evaluated by multiplying the PAH concentrations in the sample by the individual toxicity equivalency factor (TEF) as shown in [Equation 4](#i2156-9614-9-24-191204-e04){ref-type="disp-formula"}.[@i2156-9614-9-24-191204-b24] The toxicity equivalency factor is an estimate of the relative toxicity of individual PAH fractions compared to benzo(a)pyrene. Toxic equivalency factors have been applied as useful tools for the regulation of compounds with common mechanisms of action (e.g. PAHs). The TEFs developed by Nisbet and LaGoy were applied and these values were used to calculate PAH as equivalents for benzo\[a\]pyrene for a standard adult with 70 kg body weight.[@i2156-9614-9-24-191204-b25] The toxic equivalent quotient (TEQ) was derived by adding the carcinogenic potencies of individual PAHs shown in [Equation 5](#i2156-9614-9-24-191204-e05){ref-type="disp-formula"}.[@i2156-9614-9-24-191204-b24] where, B(A)Pteq is the carcinogenic potencies of individual PAHs and C~i~ is the PAH concentration. The screening value (SV) was calculated as shown in [Equation 6](#i2156-9614-9-24-191204-e06){ref-type="disp-formula"}, and then compared with the estimated TEQ value to assess the health risk of PAHs associated with consumption of the biota samples. The screening value is referred to as the threshold concentration of chemicals in edible tissue(s) that is of potential risk to consumers. It was calculated using the formula of Nozar et al.[@i2156-9614-9-24-191204-b5] where, RL is the maximum acceptable risk level (10^−5^),CSF is the oral cancer slope factor (7.3 mg/kg/day), BW is body weight (70 kg)\, and CONR is the fish consumption rate. \Body weight of 70 kg applies to the adult population.[@i2156-9614-9-24-191204-b15] Histopathological examination ----------------------------- The fish samples were dissected to remove the target organs, while the shrimps and crabs were dissected to obtain the fleshy parts. The gills, fillet, liver of fish and the fleshy parts of the crab and shrimp were put in a separate well labeled bottle, fixed in 5% formalin for at least 48 hours and transferred into a sampling bottle rack. Tissue processing for the histopathological analyses was done according to standard methods.[@i2156-9614-9-24-191204-b26] The tissues were removed from the fixative, and samples were rinsed in tap water for 5 minutes, and dehydrated in ascending ethanol concentrations (70%, 80% and 90% alcohol) for a minimum of 2 minutes each. The dehydrated tissues were cleaned in a wax miscible agent (xylene) for 2 minutes and then embedded in paraffin. Tissue sectioning and staining ------------------------------ The fish tissues were then cut into sections approximately 5 μm thick from the block using a rotary microtome (Yamato Kohki, serial no: 75010JO). The cut samples were dried in a hot air oven to remove moisture and each section was mounted on a glass slide. The sections were de-waxed in a wax-miscible agent and rehydrated through descending concentrations of ethanol (90%, 80% and 70% alcohol) for at least 2 minutes each. The sections were then stained with hematoxylin and eosin, after which the tissues were placed in hematoxylin solution for 3 minutes and aqueous eosin for 3 minutes, mounted on a slide and covered with cover slip and labeled.[@i2156-9614-9-24-191204-b27] The tissues were examined, and their microphotographs were taken using a digital binocular compound LED microscope (model MD827S30L series). Statistical analysis -------------------- The obtained data were subjected to descriptive statistics and analysis of variance. The significant treatment means were separated using Duncan\'s multiple range tests using the Statistical Package for the Social Sciences software (SPSS) version 19.0. Results ======= Concentrations of PAHs in sediment samples are presented in [Table 1](#i2156-9614-9-24-191204-t01){ref-type="table"}. A total of 17 PAHs compounds (naphthalene, 1-methylnaphthalene, 2-methylnaphthalene, acenaphthylene acenaphthene, fluorene, phenanthrene, anthracene, pyrene, fluoranthene, benzo(a)anthracene, chrysene, benzo(b)fluoranthene, benzo(k) fluoranthene, benzo(a)pyrene, indeno(1,2,3-cd) pyrene, benzo(ghi) perylene) were detected in the sediment samples. Concentration of PAHs ranged from 2.15 - 36.46 mgkg^−1^ across the sampling points. Sampling point 5 had the highest (36.46 mg/kg) concentration of PAHs compared to those detected from other points. In the present study, 47.06% of PAHs had 2--3 rings, 23.53% of PAHs had 4-rings, and 29.41% of PAHs had 5--6 rings. The percentage composition pattern of PAHs detected in the sediment samples by number of rings is presented in [Table 2](#i2156-9614-9-24-191204-t02){ref-type="table"}. The phenanthrene to anthracene (Ph/An) ratio for sediment samples were 0.65, 2.43 and 1.72 in sampling points 1, 4 and 5, respectively, but were below detection limit in points 2 and 3. The respective values for fluoranthene to pyrene (Fl/Py) ratio were 0.38, 0.66, 0.47 and 1.02 in sampling points 1, 2, 4, and 5, respectively. ###### Concentrations of PAHs in Sediment (mg/kg) PAHs Sampling locations ------------------------ -------------------- -------------- --------------- --------------- -------------- Naphthalene 1.03±0.12^a^ 1.17±0.01^a^ 0.95±0.00^ab^ 0.70±0.00^c^ 0.66±0.01^c^ 1-Methylnaphthalene 0.36±0.03^a^ 0.41±0.02^a^ 0.31±0.03^a^ 0.19±0.02^ab^ 0.23±0.00^a^ 2-Methylnaphthalene 0.23±0.06^a^ 0.27±0.01^a^ 0.19±0.03^a^ 0.15±0.03^a^ 0.12±0.00^a^ Acenaphthylene 1.42±1.11^a^ BDL BDL BDL 0.45±0.13^b^ Acenaphthene 0.23±0.19^a^ 0.09±0.01^b^ 0.03±0.01^b^ 0.04±0.01^b^ 0.05±0.01^b^ Fluorene 1.05±0.53^a^ BDL BDL BDL BDL Phenanthrene 2.00±0.19^a^ BDL BDL 0.17±0.02^c^ 0.74±0.07^b^ Anthracene 3.25±0.14^a^ BDL BDL 0.07±0.01^c^ 0.43±0.07^b^ Pyrene 5.43±0.18^a^ 0.97±0.04^c^ BDL 0.49±0.00^d^ 4.63±2.30^b^ Fluoranthene 2.07±0.08^b^ 0.64±0.02^d^ 1.63±0.01^c^ 0.23±0.02^e^ 4.73±2.10^a^ Benzo(a)anthracene 0.76±0.66^b^ BDL BDL 0.11±0.01^c^ 2.48±0.45^a^ Chrysene BDL BDL BDL BDL 4.97±2.45 Benzo(k)fluoranthene BDL BDL BDL BDL 3.03±1.44 Benzo(b)fluoranthene BDL BDL BDL BDL 2.80±1.67 Benzo(a)pyrene BDL BDL BDL BDL 4.10±1.95 Benzo(ghi)perylene BDL BDL BDL BDL 3.38±1.89 Dibenzo(a,h)anthracene BDL BDL BDL BDL BDL Indeno(1,2,3-cd)pyrene BDL BDL BDL BDL 3.67±2.34 ∑CPAHs 0.76 \- \- 0.11 20.76 Total PAHs 17.82 3.55 3.11 2.15 36.46 ^\^Mean concentrations with different superscripts along the same row are significantly different (P≤0.05). Abbreviations: BDL, below detection limit (detection limit − 0.001 mg/kg); CPAHS, carcinogenic PAH. ###### Percentage Composition of LMW and HMW of Total PAHs Detected in Sediment Samples Number of Rings \% Abundance ----------------- -------------- 2--3 ring PAHs 47.06% 4 ring PAHs 29.41% 5--6 ring PAHs 23.53% Polycyclic aromatic hydrocarbon concentrations in Drepane africana and Pomadasys jubelini ----------------------------------------------------------------------------------------- Concentration of PAHs in Drepane africana and Pomadasys jubelini samples are presented in [Table 3](#i2156-9614-9-24-191204-t03){ref-type="table"}. The concentration of total PAHs in the fillet (i.e. muscle) was 22.67 mg/kg, and 33.97 mg/kg in the whole fish in Drepane africana. For the individual PAH compounds, naphthalene had the highest concentration (28.53±9.19 mg/kg) which was observed in the whole fish sample, while anthracene had the lowest concentration (0.02±0.01 mg/kg) and was observed in the fillet of the fish sample. ###### Mean Concentrations of PAHs in Drepane africana and Pomadasys jubelini (mg/kg) PAHs Drepane africana Pomadasys jubeli ------------------------ ------------------ ------------------ -------------- ---------------- Naphthalene 19.17±20.13^b^ 28.53±9.19^a^ 9.44±3.42^b^ 27.60±12.20^a^ 1-MethylNaphthalene 1.46±0.86^b^ 1.74±0.06^a^ 0.76±0.68^b^ 2.54±2.04^a^ 2-MethylNaphthalene 0.93±0.47^a^ 1.05±0.36^a^ 0.45±0.37^b^ 1.71±1.33^a^ Acenaphthylene 0.07±0.12^a^ 0.24±0.04^a^ 0.15±0.13^a^ 0.33±0.11^a^ Acenaphthene 0.22±0.17^a^ 0.14±0.11^a^ 0.15±0.13^b^ 0.54±0.33^a^ Fluorene 0.34±0.30^a^ 0.20±0.17^ab^ 0.10±0.11^b^ 0.50±0.46^a^ Phenanthrene 0.25±0.21^ab^ 0.70±0.62^a^ 0.39±0.11^b^ 0.91±1.01^a^ Anthracene 0.02±0.01^a^ 0.17±0.16^a^ 0.08±0.06^a^ 0.02±0.01^a^ Pyrene 0.07±0.03^b^ 0.52±0.43^a^ 0.17±0.05^b^ 0.40±0.25^a^ Fluoranthene 0.14±0.11^b^ 0.69±0.44^a^ 0.20±0.07^b^ 0.48±0.35^a^ Benzo(a)anthracene BDL BDL BDL BDL Chrysene BDL BDL BDL BDL Benzo(k)fluoranthene BDL BDL BDL BDL Benzo(b)fluoranthene BDL BDL BDL BDL Benzo(a)pyrene BDL BDL BDL BDL Benzo(ghi)perylene BDL BDL BDL BDL Dibenzo(a,h)anthracene BDL BDL BDL BDL Indeno(1,2,3-cd)pyrene BDL BDL BDL BDL Total PAHs 22.67 33.97 11.89 35.02 ^\^Mean concentrations with different superscripts along the same row are significantly different at P≤0.05. Abbreviation: BDL, below detection limit (detection limit − 0.001 mg/kg) Moreover, the concentration of total PAHs in the fillet was 11.89 mg/kg and 35.02 mg/kg in the whole fish in Pomadasys jubelini samples. A total of 10 PAH compounds were detected in the samples. Naphthalene had the highest concentration (27.60±12.20 mg/kg) of individual PAH compounds and was observed in the whole fish sample, while anthracene had lowest concentration (0.02±0.01 mg/kg) and was observed in the whole fish sample. In the present study, 80% of PAHs had 2--3 rings, 20% had 4-rings, and no PAHs with 5--6 rings were detected in Drepane africana and Pomadasys jubelini samples ([Table 4](#i2156-9614-9-24-191204-t04){ref-type="table"}). ###### Percentage composition of LMW and HMW of total PAHs detected in Drepane africana and Pomadasys jubelini Number of rings \% Abundance ----------------- -------------- 2--3 ring PAHs 80% 4 ring PAHs 20% Polycyclic aromatic hydrocarbon concentrations in Callinectes amnicola (blue marine crab) and Penaeus notialis (pink shrimp) ---------------------------------------------------------------------------------------------------------------------------- Concentrations of PAHs in Callinectes amnicola and Penaeus notialis samples are presented in [Table 5](#i2156-9614-9-24-191204-t05){ref-type="table"}. A total of 9 PAHs were detected in C. amnicola, while 10 PAH congeners (naphthalene, 1-methylnaphthalene, 2-methylnaphthalene, acenaphthylene, acenaphthene, fluorene, phenanthrene, anthracene, pyrene, fluoranthene) were detected in P. notialis. All of the LMW PAHs tested for were present except for fluorene, which was not detected in crab. The concentration of total PAHs in the crab sample was 60.30 mg/kg. The highest concentration (46.50±15.66 mg/kg) of individual PAH compounds were obtained in naphthalene and the lowest concentration (0.05±0.02 mg/kg) was obtained in anthracene. The result obtained in this study (6 0030 ng/g) for crab was higher than the result reported for crab; young (1 2138.07 ng/g) and mature crabs with eggs (5629.80 ng/g) collected from Lagos lagoon.[@i2156-9614-9-24-191204-b28] In the present study, 77.78% of PAHs had 2--3 rings, 22.22% of PAHs had 4-rings, and no 5--6 ring PAHs were detected in Callinectes amnicola and Penaeus notialis samples. Concentration of PAHs in shrimp ranged from 0.08±0.13 to 50.65 ± 21.88 mgkg^−1^. The highest concentration was found in naphthalene and lowest concentration was found in acenaphthylene.[@i2156-9614-9-24-191204-b29]The percentage composition pattern of PAHs detected in the samples by the number of rings is shown in [Table 6](#i2156-9614-9-24-191204-t06){ref-type="table"}. ###### Concentrations of PAHs in Callinectes amnicola and Penaeus notialis (mg/kg) Wet Weight PAHs Crab Shrimp ------------------------- ---------------- ---------------- Naphthalene 46.50±15.66^b^ 50.65±21.88^a^ 1-Methylnaphthalene 7.01±8.38^a^ 6.57±7.82^b^ 2-Methylnaphthalene 4.70±5.94^a^ 4.21±5.27^b^ Acenaphthylene 0.18±0.16^a^ 0.08±0.13^a^ Acenaphthene 0.29±0.15^b^ 1.31±1.72^a^ Fluorene BDL 1.78±3.07 Phenanthrene 0.79±1.02^b^ 1.65±2.04^a^ Anthracene 0.05±0.02^b^ 3.34±2.10^a^ Pyrene 0.27±0.16^b^ 0.57±0.59^a^ Fluoranthene 0.51±0.29^b^ 0.91±1.20^a^ Benzo(a)anthracene BDL BDL Chrysene BDL BDL Benzo(k)fluoranthene BDL BDL Benzo(b)fluoranthene BDL BDL Benzo(a)pyrene BDL BDL Benzo(ghi)perylene BDL BDL Dibenz(a,h)anthracene BDL BDL Indeno(-1,2,3-cd)pyrene BDL BDL Total PAHs 60.30 71.06 ^\^Mean concentrations with different superscripts along the same row are significantly different at P≤0.05. Abbreviation: BDL, below detection limit (detection limit − 0.001 mg/kg) ###### Percentage composition of PAHs in samples of Callinectes amnicola and Penaeus notialis Number of Rings \% Abundance ----------------- -------------- 2--3 ring PAHs 77.78% 4 ring PAHs 22.22% Health risk assessment ---------------------- The estimated dietary intake values of total PAHs for fillet and whole fish were 1.55 and 2.33 mg/kg body weight/day, respectively. The fish consumption rate was set at 0.0685 kg/day from the annual per capita fish consumption of 25 kg for Nigeria.[@i2156-9614-9-24-191204-b15] The values obtained in this study exceeded the values reported for fish samples from Degele community, Sapele, Nigeria which was reported to be 0.02 - 0.94 mg/kg body weight/day (O. niloticus), 0.02--0.12 mg/kg body weight/day (C. gariepinus), 0.12--0.16 mg/kg body weight/day (H. longifilis) and 0.14--0.58 mg/kg body weight/day (L. falcipinnis), respectively.[@i2156-9614-9-24-191204-b30] The estimated dietary intakes of sampled fish species are shown in [Table 7](#i2156-9614-9-24-191204-t07){ref-type="table"}. ###### Estimated Dietary Intake of PAHs from Sampled Organisms Organisms Estimated dietary Intake (mgkg; body weight/day) ----------------------------- -------------------------------------------------- Drepane Afrieana (fillet) 1.55 Drepane Afrieana (whole) 2.33 Pomadasys jubelini (fillet) 0.81 Pomadasys jubelini (whole) 2.40 Crab 0.10 Shrimp 1.56 Dietary intake of polycyclic aromatic hydrocarbons from Callinectes amnicola and Penaeus notialis ------------------------------------------------------------------------------------------------- The estimated dietary intake values of total PAHs for crab and pink shrimp were 0.10 and 1.56 mg/kg body, respectively. The carcinogenic potencies of individual PAHs and TEQ values are presented in [Table 8](#i2156-9614-9-24-191204-t08){ref-type="table"}. The TEQ values obtained from TEF values were used to assess the carcinogenicity of PAH contamination in the sampled biota.[@i2156-9614-9-24-191204-b31] The TEQ values of PAHs in the biota samples were 6.08×10^−2^, 1.01×10^−1^, 2.29×10^−2^, 3.55 × 10^−2^, 1.26×10^−2^ and 3.52×10^−2^ mg/kg for crab, shrimp, Drepane africana (fillet), Drepane africana (whole), Pomadasys jubelini (fillet), Pomadasys jubelini (whole), respectively. ###### Carcinogenic Potencies of Individual PAHs and Toxic Equivalent Quotient Values B(a)Pteq values (mg/kg) ------------------------- ------- ------------- ------------- -------------- ------------- ------------- ------------- Naphthalene 1- 0.001 4.67×10^−2^ 5.06×10^−2^ 1.92×10^−2^ 2.85×10^−2^ 9.44×10^−3^ 2.76×10^−2^ Methylnaphthalene 2- 0.001 7.00×10^−3^ 6.57×10^−3^ 1.46×10^−3^ 1.74×10^−3^ 7.60×10^−4^ 2.54×10^−3^ Methylnaphthalene 0.001 5.00×10^−3^ 4.21×10^−3^ 9.30×10^−4^ 1.05×10^−3^ 4.50×10^−4^ 1.71×10^−3^ Acenaphthylene 0.001 1.8×10^−4^ 8.00×10^−5^ 7.00×10^−5;^ 2.40×10^−4^ 1.50×10^−4^ 3.30×10^−4^ Acenaphthene 0.001 2.9×10^−4^ 1.31×10^−3^ 2.20×10^−4^ 1.40×10^−3^ 1.50×10^−4^ 5.40×10^−4^ Fluorene 0.001 \- 1.78×10^−3^ 3.40×10^−4^ 2.00×10^−4^ 1.00×10^−4^ 5.00×10^−4^ Phenanthrene 0.001 7.9×10^−4^ 1.65×l0^−3^ 2.50×10^−4^ 7.00×10^−4^ 3.90×10^−4^ 9.10×10^−4^ Anthracene 0.01 5.00×10^−4^ 3.34×10^−3^ 2.00×10^−4^ 1.70×10^−3^ 8.00×10^−4^ 2.00×10^−4^ Pyrene 0.001 2.70×10^−4^ 5.70×10^−4^ 7.00×10^−5^ 5.20×10^−4^ 1.70×10^−4^ 4.00×10^−4^ Fluoranthene 0.001 5.1 ×10^−4^ 9.10×10^−4^ 1.40×10^−4^ 6.90×10^−4^ 2.00×10^−4^ 4.80×10^−4^ TEQ (values mg/kg) 6.08×10^−2^ 1.01×10^−1^ 2.29×10^−2^ 3.55×10^−2^ 1.26×10^−2^ 3.52×10^−2^ Abbreviation: B(a)Pteq, carcinogenic potencies of individual PAHs Carcinogenic potency of individual polycyclic aromatic hydrocarbons and toxic equivalent quotient ------------------------------------------------------------------------------------------------- The carcinogenic potencies of individual PAHs and TEQ values are presented in [Table 8](#i2156-9614-9-24-191204-t08){ref-type="table"}. The TEFs method was developed to evaluate structurally related compounds and has been applied as a useful tool for the regulation of compounds with a common mechanism of actions (e.g. PAHs). The TEF is an estimate of the relative toxicity of an individual PAH fraction compared to benzo(a)pyrene. The TEF values are used to calculate other PAHs to benzo(a)pyrene equivalents (the most toxic PAHs) for an average adult with 70 kg body weight.[@i2156-9614-9-24-191204-b24] The carcinogenic potency of individual PAHs is represented by the value resulting from the product of the concentration and TEF value of each congener. The TEQ value is the summation of carcinogenic potencies of individual PAH values obtained from a particular sample. It expresses an aggregate measure of toxicity based on a number of contributing compounds. Screening value --------------- The SV was evaluated to assess the health risks posed by PAHs to humans from consuming the sampled organisms. The screening value is defined as the threshold concentration of chemicals in edible tissue that is of potential public health concern.[@i2156-9614-9-24-191204-b16],[@i2156-9614-9-24-191204-b32] An estimated SV of 0.0599, 0.0044 and 0.0014 mg/kg was obtained for crab, shrimp and fish samples, respectively. The resulting TEQ values obtained for the sampled biota exceeded the screening values ([Figure 6](#i2156-9614-9-24-191204-f06){ref-type="fig"}). ![Comparison between TEQ and screening values](i2156-9614-9-24-191204-f06){#i2156-9614-9-24-191204-f06} Histopathological examination ----------------------------- In the present study, the major changes observed in the gills of Drepane africana and Pomadasys jubelini were hypertrophy of the primary lamellae and hyperplasia of the secondary lamellae. Shortening and fusion of the secondary lamellae were observed in Drepane africana, while hyperplasia of the epithelial cells was observed in Pomadasys jubelini. In the muscle of Drepane africana and Pomadasys jubelini, splitting and atrophy of the muscle bundles were observed, while necrosis of the muscle bundles was seen in Pomadasys jubelini only ([Figures 7a](#i2156-9614-9-24-191204-f07a){ref-type="fig"}--[c](#i2156-9614-9-24-191204-f07c){ref-type="fig"}).* Splitting of the muscle myofibrils was observed in shrimp only, while splitting and atrophy of the muscle bundles were observed in the muscles of shrimp and crab ([Figures 8a](#i2156-9614-9-24-191204-f08a){ref-type="fig"}--[b](#i2156-9614-9-24-191204-f08b){ref-type="fig"} and [9](#i2156-9614-9-24-191204-f09){ref-type="fig"}). Changes observed in the liver of Drepane africana and Pomadasys jubelini included necrosis, hepatopancreas and cellular degeneration ([Figure 10a](#i2156-9614-9-24-191204-f10a){ref-type="fig"}--[d](#i2156-9614-9-24-191204-f10d){ref-type="fig"}). ![Photomicrograph of muscle section in Drepane africana showing atrophy of muscle bundles (AMB) (Mag. ×100)](i2156-9614-9-24-191204-f07a){#i2156-9614-9-24-191204-f07a} ![Photomicrograph of muscle section in Drepane africana showing splitting of muscle (SMB) (Mag. ×400)](i2156-9614-9-24-191204-f07b){#i2156-9614-9-24-191204-f07b} ![Photomicrograph of muscle section in Pomadasys jubelini showing necrosis of muscle bundles (NMB) (Mag. ×100)](i2156-9614-9-24-191204-f07c){#i2156-9614-9-24-191204-f07c} ![Photomicrograph of muscle section in Penaeus notialis (pink shrimp) showing atrophy of muscle bundles (AMB) (Mag. ×40)](i2156-9614-9-24-191204-f08a){#i2156-9614-9-24-191204-f08a} ![Photomicrograph of muscle section in Penaeus notialis (pink shrimp) showing splitting of muscle (SMB), and splitting of muscle myofibril (SMM) (Mag. ×100)](i2156-9614-9-24-191204-f08b){#i2156-9614-9-24-191204-f08b} ![Photomicrograph of muscle section in Callinectes amnicola (blue marine crab) showing necrosis of muscle bundles (NMB) and splitting of muscle (SMB) (Mag. ×40)](i2156-9614-9-24-191204-f09){#i2156-9614-9-24-191204-f09} ![Photomicrograph of liver section in Drepane africana showing focal area hepatopancreas of necrosis (Mag. ×100) degeneration](i2156-9614-9-24-191204-f10a){#i2156-9614-9-24-191204-f10a} ![Photomicrograph of liver section in Drepane africana showing degeneration (HD) and cellular (CD) (Mag. ×100) degeneration](i2156-9614-9-24-191204-f10b){#i2156-9614-9-24-191204-f10b} ![Photomicrograph of liver section in Drepane africana showing focal area hepatopancreas degeneration (HD) (Mag. ×100)](i2156-9614-9-24-191204-f10c){#i2156-9614-9-24-191204-f10c} ![Photomicrograph of liver section in Drepane africana showing the nucleus (N) and hepacytes (H) (Mag. ×100)](i2156-9614-9-24-191204-f10d){#i2156-9614-9-24-191204-f10d} Discussion ========== The predominance of LMW and HMW PAHs in the sediments reflects the presence of significant combustion products from pyrolytic processes and/or petrogenic sources.[@i2156-9614-9-24-191204-b33],[@i2156-9614-9-24-191204-b34] The preponderance of LMW and HMW PAHs in the sediments indicates the presence of significant combustion products from pyrolytic processes and/or petrogenic sources. [@i2156-9614-9-24-191204-b33],[@i2156-9614-9-24-191204-b34] A sediment quality guideline of 1000 ng/g dry weight total PAHs was designed to protect estuarine fish against several important health effects.[@i2156-9614-9-24-191204-b35] Based on this guideline, the results of this study showed that the concentrations of total PAHs exceeded 1000 ng/g dry weight at all sampling points, indicating that aquatic organisms in the region could be at severe health and environmental risk. Polycyclic aromatic hydrocarbon concentrations in soil/sediment can be classified according to the following categories: \>1.0 mg/kg, 0.001 -- 1.0 mg/kg and \< 0.001 mg/kg for high risk, medium risk, and low risk, respectively.[@i2156-9614-9-24-191204-b36] In the present study, the concentration of PAHs from all sampling points were higher than 1.0 mg/kg, indicating that they presented a high risk. All sediment samples exceeded the USEPA guideline value of 2.5 mg/kg except sampling point 4, which was slightly lower (2.15 mg/kg) ([Table 1](#i2156-9614-9-24-191204-t01){ref-type="table"}). In rural areas, PAHs adsorbed in atmospheric particles can be deposited on the surface of lakes, streams, and oceans by dry or wet deposition, where they could be dispersed by currents and eventually become integrated with sediment. Sediments near urban centers are influenced by atmospheric deposition of PAHs. Other sources of PAHs include storm and sanitary sewer effluents as well as roadway runoff. It was observed that the concentration of PAHs was higher in sediment samples than in water samples. This could be attributed to their hydrophobic tendencies and propensity towards adsorption to particles and solid phases. In addition, they settle and become part of the sedimentary record. Anthropogenic PAHs originate mainly from combustion of fossil fuels and spillage of petroleum products; from fuel combustion (pyrolytic) or from crude oil (petrogenic). Contamination may be identified by ratios of individual PAH compounds based on peculiarities in PAH composition and distribution patterns as a function of the emission source. Ratios of Ph/An and Fl/Py have been widely used to distinguish petrogenic and pyrogenic sources of PAHs.[@i2156-9614-9-24-191204-b37],[@i2156-9614-9-24-191204-b38] Polycyclic aromatic hydrocarbons of petrogenic origin are generally characterized by Ph/An values \> 10, whereas combustion processes often result in low Ph/An ratio \< 10. For the Fl/Py ratio, values \> 1 have been used to indicate pyrolytic origins and values \< 1 are attributed to petrogenic sources. The results from both Ph/An and Fl/Py ratios indicated that PAHs in the Atlas Cove jetty area may originate from both pyrolytic and petrogenic sources. It was observed that the PAHs have pyrolytic sources in sediment samples in all sampling points and this may be attributed to high ship traffic. Potential toxicity of PAHs in sediments on the surrounding aquatic organisms was assessed. The PAHs concentration in the sediments were compared with US National Oceanic sediment quality guidelines ([Table 9](#i2156-9614-9-24-191204-t09){ref-type="table"}).[@i2156-9614-9-24-191204-b39] The recommended effect range low (ERL) and effect range median (ERM) target values were used to determine toxic effects in the sampling locations. When PAH concentrations vary between ERL and ERM values, a mild toxic effect is expected. In addition, no negative effect is expected for PAH concentrations lower than ERL values. [Table 9](#i2156-9614-9-24-191204-t09){ref-type="table"} indicates a high probability of risk for organisms that live in sampling locations 1 and 5. Naphthalene, acenaphthene, and fluoranthene exceeded the ERL values, but were within ERM values in both sampling locations, indicating a mild toxic effect. Anthracene exceeded the ERL and ERM values at sampling locations 1 and 5, but was within ERM value at sampling location 5. Anthracene, phenanthrene, pyrene and fluoranthene were below ERL values in sampling location 4. Anthracene, fluorene, phenanthrene, acenaphthylene and pyrene in sampling location 1 and pyrene and benzo(a)pyrene in sampling location 5 exceeded ERM values, suggesting that adverse biological effects such as cancer, reproductive and physiological disorder may occur in fish and mammals.[@i2156-9614-9-24-191204-b40] ###### Concentrations of PAHs in Sediment Compared with US National Oceanic Sediment Quality Guidelines PAHs ERL[@i2156-9614-9-24-191204-b39] (ngg-^1^) ERM[@i2156-9614-9-24-191204-b39] (nss-^1^) Sampling locations ------------------------ -------------------------------------------- -------------------------------------------- -------------------- ------ ------ ----- ------ Naphthalene 160 2100 1030 1170 950 700 660 Anthracene 85 1100 3250 \- \- 70 430 Fluorene 19 540 1050 \- \- \- \- Phenanthrene 240 1500 2000 \- \- 170 740 Acenaphthene 16 500 230 90 30 40 50 Acenaphthylene 44 640 1420 \- \- \- 450 Pyrene 665 2600 5430 970 1630 490 4630 Fluoranthene 600 5100 2070 640 \- 230 4730 Benzo (b) fluoranthene \- \- \- \- \- \- 2800 Benzo(a) pyrene 430 2800 \- \- \- \- 4100 Abbreviations: ERL, effective range low; ERM, effective range median. Polycyclic aromatic hydrocarbons concentrations in Drepane africana and Pomadasys jubelini ------------------------------------------------------------------------------------------ A total of 10 PAH compounds (naphthalene, 1-methylnaphthalene, 2-methylnaphthalene, acenaphthylene, acenaphthene, fluorene, phenanthrene, anthracene, pyrene, fluoranthene) were detected in the samples ([Table 3](#i2156-9614-9-24-191204-t03){ref-type="table"}). The less carcinogenic LMW PAHs were detected with naphthalene and its substituent present in the fish samples. The more carcinogenic HMW PAHs (benzo(a)anthracene, chrysene, benzo(k)fluoranthene, benzo(b)fluoranthene, benzo(ghi) perylene, dibenzo(a,h)anthracene, indeno(1,2,3-cd)pyrene) were not detected in the samples of Drepane africana. This result agreed with the report of PAHs in fish samples from the Degele community of Delta state, Nigeria and the bioaccumulation of PAHs in fish and invertebrates of Lagos lagoon.[@i2156-9614-9-24-191204-b30],[@i2156-9614-9-24-191204-b41] A significant (P≤0.05) difference was observed in the total PAH concentrations between fillet and whole fish of the fish species. The percentage composition pattern of PAHs detected in the samples by number of rings is shown in [Table 4](#i2156-9614-9-24-191204-t04){ref-type="table"}. The predominance of LMW PAHs as compared to HMW PAHs in the fish samples reflects the presence of significant petrogenic processes.[@i2156-9614-9-24-191204-b33],[@i2156-9614-9-24-191204-b34] The analysis showed that a total of 10 PAHs (8 of which are among the 16 PAHs prioritized by the USEPA) were present in the fish sample. The concentration of PAHs in fish was higher than the water column; this could be due to the fact that PAHs are more readily absorbed by fish than other aquatic organisms on exposure to contaminated materials, thus attaining elevated levels compared to those in the surrounding medium.[@i2156-9614-9-24-191204-b6] The trend for the less carcinogenic LMW PAHs and the more carcinogenic HMW PAHs in Pomadasys jubeli was similar to that observed in Drepane africana presented above. The concentration of total PAHs was lower in the whole fish and fillet of both fish species compared to that of crab and shrimp in the present study. This may be because fish have been reported to have physiological mechanism(s) of rapid PAH biotransformation or depuration and could be influenced by various factors, such as chemical exposure route and time, lipid content of tissues, environmental factors, exposure to multiple contaminants, and differences in species, age, sex, and health conditions of the test animals.[@i2156-9614-9-24-191204-b28] The biotransformation of hydrophobic-containing substances in fish is a major determinant of its toxicity, distribution and excretability.[@i2156-9614-9-24-191204-b6] A large percentage of the world\'s population depends on seafood, especially fish, to meet their nutritional requirements. In Nigeria, fish provides over 60% of protein intake and is recognized as a very important source of animal protein. Food consumption has been identified as an important pathway of human exposure to many contaminants, including PAHs. Due to the lipophilic nature and high chemical stability of PAHs, they accumulate in the fatty tissues of fish following their uptake.[@i2156-9614-9-24-191204-b42] Exposure pathways of PAHs to fish include bioconcentration from water across their gills, skin and ingestion of PAH-contaminated particulate matter along with food, as PAHs readily adsorb onto particulate organic matter especially soil sediments.[@i2156-9614-9-24-191204-b15] The concentrations of contaminants such as PAHs in fish reflect the state of contamination of the environment.[@i2156-9614-9-24-191204-b43] The observed concentrations of total PAHs in fish in this study indicate high levels of PAHs contamination around the Atlas Cove jetty. Polycyclic aromatic hydrocarbon concentrations in Callinectes amnicola (blue marine crab) ----------------------------------------------------------------------------------------- Crabs have been reported to have high lipid contents and this increases the chance of absorbing more hydrocarbon molecules, especially those that are not easily degraded or eliminated. The higher concentration of PAHs observed in the present study may be due to the proximity of the sampling points to the Atlas Cove jetty or the movement of ships along the waterways which may serve as a source of pollution. However, PAH concentrations were lower than the values (101.10 - 151.49 μg/g) reported for crabs (Callinectes sapidus) obtained from the coastal area of Ondo State, Nigeria.[@i2156-9614-9-24-191204-b29] The higher levels of PAHs in shrimps are presumably due to food chain bioaccumulation and can be harmful to human health. The concentration of PAHs in crab and shrimp were significant and may have wide environmental implications, affecting bioconcentration in their tissues due to their inability to metabolize PAHs efficiently. The relatively higher concentrations of total PAHs in tissues of shellfish than fish showed the bioaccumulative potency of PAHs by the studied organisms. It may also be due to the fact that shrimps and crabs live directly on and forage in the sediments, whereas fish live up in the water column. Several aquatic organisms such as bivalves, crabs, and shrimps have been reported to bioaccumulate and bioconcentrate organic pollutants in their target organs at levels higher than background concentrations.[@i2156-9614-9-24-191204-b44],[@i2156-9614-9-24-191204-b45] Therefore, they are excellent bioaccumulators of organic and inorganic pollutants. Higher concentrations of total PAHs in banana shrimp and blue crab were compared to Drepane punctata and Pomadasys kaakan, which had lower concentrations of PAHs.[@i2156-9614-9-24-191204-b5] Health risk assessment ---------------------- The consumption of Drepane africana at the rate of 68 g/day may induce adverse health effects over time in consumers. Dietary intake of polycyclic aromatic hydrocarbons from Pomadasys jubelini ---------------------------------------------------------------------------- The estimated dietary intake values in the present study (0.81 for fillet and 2.40 mg/kg body weight/day for whole fish) were considerably higher in comparison with values reported in other countries of 1.77 - 10.7 ng/kg body weight/day, 626 - 712 ng/day, 13.8 - 16.7 ng/kg body weight/day and 231 ng/day for Mumbai, India, Spain, Korea and Kuwait, respectively.[@i2156-9614-9-24-191204-b33],[@i2156-9614-9-24-191204-b46],[@i2156-9614-9-24-191204-b47] Comparison of toxic equivalency quotient values ----------------------------------------------- The lowest TEQ value was obtained in the fillet of Pomadasys jubelini. The TEQ values of PAHs in fish species, as reported by Tongo et al. were 0.22, 0.005, 0.30 and 0.03 mg/kg in Clarias gariepinus, Tilapia zilli, Ethmalosa fimbriata, and Scomber scombrus, respectively.[@i2156-9614-9-24-191204-b24] The consumption of species with the lowest total mean concentrations of PAHs have a higher potential to cause carcinogenic risk, which agrees with the findings of the present study. Furthermore, the calculated TEQ values were in agreement with the values reported by Iwegbue et al.[@i2156-9614-9-24-191204-b41] The results of the present study are in agreement with a study of PAHs contaminants in Chrysichthys nigrodigitatus in Rivers State, Nigeria, where Patrolecco et al. reported TEQ values above estimated SVs.[@i2156-9614-9-24-191204-b48],[@i2156-9614-9-24-191204-b49] In addition, higher TEQ values were reported when compared to calculated SVs for PAHs in seafood (fish, crab, and bivalves) in Iran, indicating potential health effects.[@i2156-9614-9-24-191204-b5] However, these results disagreed with reports of lower estimated TEQ values than the SV in studies of PAH concentrations in fish (feral finfish) from a Hong Kong market and the common eel (Anguilla anguilla) from the River Tiber, Italy.[@i2156-9614-9-24-191204-b16],[@i2156-9614-9-24-191204-b49] Histopathological examination ----------------------------- Histopathological biomarkers are sensitive indicators of subcellular stress in organisms exposed to a range of pollutants over short and long periods of time.[@i2156-9614-9-24-191204-b50] Changes caused by toxic substances can be observed in the gills, such as an increase in pollutant blood diffusion distance as a means for protection.[@i2156-9614-9-24-191204-b50] Fusion of secondary lamellae, which is a result of hyperplasia, brings about a reduction in free gas exchange, thus affecting the general health of the fish. Hypertrophy of the primary lamellae is the enlarging or increase in size of the organ in response to a stressor in the environment. This observation is similar to a report of a high incidence of hyperplasia in Clarias gariepinus and Oreochromis niloticus reported from the Sanyati basin in Lake Kariba, Zimbabwe, as well as hyperplasia in the gills of two species of sturgeons.[@i2156-9614-9-24-191204-b50],[@i2156-9614-9-24-191204-b51] This result is an indication that the fish have been exposed to stressors. Gills are sensitive organs which are easily damaged by numerous pollutants, even at low concentrations. Gills have been reported to perform various vital functions (respiration, osmoregulation, acid-base balance). Gills have a large surface area in contact with the external environment and are particularly sensitive to chemical and physical changes of the aquatic environment, thereby being a target organ in fish for pollutants carried by water.[@i2156-9614-9-24-191204-b51],[@i2156-9614-9-24-191204-b52] Changes in the structures of these organs as well as in the vital functions performed by the gills were observed due to toxic substances present in the aquatic environment.[@i2156-9614-9-24-191204-b53] The severity of damage depends on the concentration of toxicants and the period of exposure. With prolonged exposure, these lesions could lead to fish mortality. The observed separation of muscle bundles may be due to the initial stimulus of hexachlorocyclohexane, which can induce hyperactivity and excitability in animals, leading to a release of lactic acid and subsequent muscular fatigue. The atrophy observed in the muscle bundles may be due to the exposure to various contaminants.[@i2156-9614-9-24-191204-b54] A study detected changes in muscle tissue of grass carp (Ctenopharyngodon idella) as swelling and necrosis of muscle bundles due to the effect of rice herbicides.[@i2156-9614-9-24-191204-b55] Another study documented physiological disturbances and morphological damage in the muscle tissue of freshwater fish Hoplias malabaricus collected from Ponta Lake in southern Brazil due to bioaccumulation of chlorinated pesticides and PCBs.[@i2156-9614-9-24-191204-b56] Degeneration of muscle bundles with aggregation of inflammatory cells between them and focal areas of necrosis were observed by Gingerich.[@i2156-9614-9-24-191204-b57] The findings of the present study agreed with these previous reports. The liver is the largest organ in the body and performs several important physiological functions.[@i2156-9614-9-24-191204-b58] Although every tissue has some ability to metabolize chemicals, the liver is the major organ of metabolism or transformation of toxins, making it a target organ that is highly affected by toxins in the system. Necrosis is the death of cells in a tissue or organ caused by disease or injury or as a result of exposure to harmful or toxic contaminants. The necrotic cells are shrunk, and their intercellular attachments are broken.[@i2156-9614-9-24-191204-b58] Vascular dilation may be responsible for the cellular degeneration and necrosis in the liver. When the liver is damaged, excessive blood flows into the liver, blocking the sinusoids. Oxygen deficiency as a result of gill degeneration is the most common cause of cellular degeneration in the liver ([Figures 9a--d](#i2156-9614-9-24-191204-f09){ref-type="fig"}).[@i2156-9614-9-24-191204-b59] The results of this study agreed with previous reports on the effects of different pollutants on fish liver.[@i2156-9614-9-24-191204-b54],[@i2156-9614-9-24-191204-b60] Conclusions =========== In the present study, low and high molecular weights PAHs were present in the sediment samples. The concentration of total PAHs in the sediment samples exceeded safe limits, suggesting that the aquatic organisms around Atlas Cove may pose serious human health and environmental risks. The high ratio of LMW PAHs as compared to HMW PAHs suggests that PAH contamination around Atlas Cove may be of natural origin. The concentration of total PAHs in biota samples indicated that PAH contamination from Atlas Cove was relatively high (with dominance of the low molecular weight PAHs). The high concentration of total PAHs present in the organisms indicated that the compounds have bioaccumulated in their tissues and organs over a period of time. The calculated TEQ values were higher than the screening values, indicating potential health effects. Histopathological examination revealed that both fish and shellfish were exposed to high concentrations of PAHs which brought about changes in morphologic structure of these organs, necrosis of the muscle bundles and cellular degeneration. 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Ataxia–telangiectasia Ataxia–telangiectasia (AT or A–T), also referred to as ataxia–telangiectasia syndrome or Louis–Bar syndrome, is a rare, neurodegenerative, autosomal recessive disease causing severe disability. Ataxia refers to poor coordination and telangiectasia to small dilated blood vessels, both of which are hallmarks of the disease. A–T affects many parts of the body: It impairs certain areas of the brain including the cerebellum, causing difficulty with movement and coordination. It weakens the immune system, causing a predisposition to infection. It prevents repair of broken DNA, increasing the risk of cancer. Symptoms most often first appear in early childhood (the toddler stage) when children begin to sit or walk. Though they usually start walking at a normal age, they wobble or sway when walking, standing still or sitting. In late pre-school and early school age, they develop difficulty moving their eyes in a natural manner from one place to the next (oculomotor apraxia). They develop slurred or distorted speech, and swallowing problems. Some have an increased number of respiratory tract infections (ear infections, sinusitis, bronchitis, and pneumonia). Because not all children develop in the same manner or at the same rate, it may be some years before A–T is properly diagnosed. Most children with A–T have stable neurologic symptoms for the first 4–5 years of life, but begin to show increasing problems in early school years. A–T is caused by a defect in the ATM gene, which is involved in the recognition and repair of damaged DNA. The prevalence of A–T is estimated to be as high as 1 in 40,000 to as low as 1 in 300,000 people. Symptoms There is substantial variability in the severity of features of A–T among affected individuals, and at different ages. The following symptoms or problems are either common or important features of A–T: Ataxia (difficulty with control of movement) that is apparent early but worsens in school to pre-teen years Oculomotor apraxia (difficulty with coordination of head and eye movement when shifting gaze from one place to the next) Involuntary movements Telangiectasia (dilated blood vessels) over the white (sclera) of the eyes, making them appear bloodshot. These are not apparent in infancy and may first appear at age 5–8 years. Telangiectasia may also appear on sun-exposed areas of skin. Problems with infections, especially of the ears, sinuses and lungs Increased incidence of cancer (primarily, but not exclusively, lymphomas and leukemias) Delayed onset or incomplete pubertal development, and very early menopause Slowed rate of growth (weight and/or height) Drooling particularly in young children when they are tired or concentrating on activities Dysarthria (slurred, slow, or distorted speech sounds) Diabetes in adolescence or later Premature changes in hair and skin Many children are initially misdiagnosed as having cerebral palsy. The diagnosis of A–T may not be made until the preschool years when the neurologic symptoms of impaired gait, hand coordination, speech and eye movement appear or worsen, and the telangiectasia first appear. Because A–T is so rare, doctors may not be familiar with the symptoms, or methods of making a diagnosis. The late appearance of telangiectasia may be a barrier to the diagnosis. It may also take some time before doctors consider A–T as a possibility because of the early stability of symptoms and signs. Ataxia and other neurologic problems The first indications of A–T usually occur during the toddler years. Children start walking at a normal age, but may not improve much from their initial wobbly gait. Sometimes they have problems standing or sitting still and tend to sway backward or from side to side. In primary school years, walking becomes more difficult, and children will use doorways and walls for support. Children with A–T often appear better when running or walking quickly in comparison to when they are walking slowly or standing in one place. Around the beginning of their second decade, children with the more severe ("classic") form of A–T start using a wheelchair for long distances. During school years, children may have increasing difficulty with reading because of impaired coordination of eye movement. At the same time, other problems with fine-motor functions (writing, coloring, and using utensils to eat), and with slurring of speech (dysarthria) may arise. Most of these neurologic problems stop progressing after the age of about 12 – 15 years, though involuntary movements may start at any age and may worsen over time. These extra movements can take many forms, including small jerks of the hands and feet that look like fidgeting (chorea), slower twisting movements of the upper body (athetosis), adoption of stiff and twisted postures (dystonia), occasional uncontrolled jerks (myoclonic jerks), and various rhythmic and non-rhythmic movements with attempts at coordinated action (tremors). Telangiectasia Prominent blood vessels (telangiectasia) over the white (sclera) of the eyes usually occur by the age of 5–8 years, but sometimes appear later or not at all. The absence of telangiectasia does not exclude the diagnosis of A–T. Potentially a cosmetic problem, the ocular telangiectasia do not bleed or itch, though they are sometimes misdiagnosed as chronic conjunctivitis. It is their constant nature, not changing with time, weather or emotion, that marks them as different from other visible blood vessels. Telangiectasia can also appear on sun-exposed areas of skin, especially the face and ears. They occur in the bladder as a late complication of chemotherapy with cyclophosphamide, have been seen deep inside the brain of older people with A–T, and occasionally arise in the liver and lungs. Immune problems About two-thirds of people with A–T have abnormalities of the immune system. The most common abnormalities are low levels of one or more classes of immunoglobulins (IgG, IgA or IgE subclasses), not making antibodies in response to vaccines or infections, and having low numbers of lymphocytes (especially T-lymphocytes) in the blood. Some people have frequent infections of the upper (colds, sinus and ear infections) and lower (bronchitis and pneumonia) respiratory tract. All children with A–T should have their immune systems evaluated to detect those with severe problems that require treatment to minimize the number or severity of infections. Some people with A–T need additional immunizations (especially with pneumonia and influenza vaccines), antibiotics to provide protection (prophylaxis) from infections, and/or infusions of immunoglobulins (gamma globulin). The need for these treatments should be determined by an expert in the field of immunodeficiency or infectious diseases. Cancer People with A–T have a highly increased incidence (approximately 25% lifetime risk) of cancers, particularly lymphomas and leukemia, but other cancers can occur. When possible, treatment should avoid the use of radiation therapy and chemotherapy drugs that work in a way that is similar to radiation therapy (radiomimetic drugs), as these are particularly toxic for people with A–T. The special problems of managing cancer are sufficiently complicated that treatment should be done only in academic oncology centers and after consultation with physicians who have specific expertise in A–T. Unfortunately, there is no way to predict which individuals will develop cancer. Because leukemia and lymphomas differ from solid tumors in not progressing from solitary to metastatic stages, there is less need to diagnose them early in their appearance. Surveillance for leukemia and lymphoma is thus not helpful, other than considering cancer as a diagnostic possibility whenever possible symptoms of cancer (e.g. persistent swollen lymph glands, unexplained fever) arise. Women who are A–T carriers (who have one mutated copy of the ATM gene), have approximately a two-fold increased risk for the development of breast cancer compared to the general population. This includes all mothers of A–T children and some female relatives. Current consensus is that special screening tests are not helpful, but all women should have routine cancer surveillance. Skin A–T can cause features of early aging such as premature graying of the hair. It can also cause vitiligo (an auto-immune disease causing loss of skin pigment resulting in a blotchy “bleach-splashed” look), and warts which can be extensive and recalcitrant to treatment. A small number of people develop a chronic inflammatory skin disease (granulomas). Lung disease Chronic lung disease develops in more than 25% of people with A–T. Three major types of lung disease can develop: (1) recurrent and chronic sinopulmonary infections; (2) lung disease caused by ineffective cough, swallowing dysfunction, and impaired airway clearance; and (3) restrictive interstitial lung disease. It is common for individuals with A–T to have more than one of these lung conditions. Chronic lung disease can occur because of recurrent lung infections due to immunodeficiency. Individuals with this problem are at risk of developing bronchiectasis, a condition in which bronchial tubes are permanently damaged, resulting in recurrent lower airway infections. Gamma globulin for people with antibody deficiency and/or chronic antibiotic treatment may reduce the problems of infection. Other individuals with A–T have difficulty with taking deep breaths and may have an ineffective cough, making it difficult to clear oral and bronchial secretions. This can lead to prolonged respiratory symptoms following common viral respiratory illnesses. Techniques that allow clearance of mucus can be helpful in some individuals during respiratory illnesses. Some people will develop swallowing problems as they age, increasing their risk of aspiration pneumonia. Recurrent injury to the lungs caused by chronic infections or aspiration may cause lung fibrosis and scarring. This process may be enhanced by inadequate tissue repair in ATM-deficient cells. A small number of individuals develop interstitial lung disease. They have decreased pulmonary reserve, trouble breathing, a need for supplemental oxygen and chronic cough in the absence of lung infections. They may respond to systemic steroid treatment or other drugs to reduce inflammation. Lung function tests (spirometry) should be performed at least annually in children old enough to perform them, influenza and pneumococcal vaccines given to eligible individuals, and sinopulmonary infections treated aggressively to limit the development of chronic lung disease. Feeding, swallowing, and nutrition Feeding and swallowing can become difficult for people with A–T as they get older. Feeding refers to all aspects of eating and drinking, including getting food and liquids to the mouth; swallowing refers to ingestion or what happens after food or liquids enter the mouth. Primary goals for feeding and swallowing are safe, adequate, and enjoyable mealtimes. Involuntary movements may make feeding difficult or messy and may excessively prolong mealtimes. It may be easier to finger feed than use utensils (e.g., spoon or fork). For liquids, it is often easier to drink from a closed container with a straw than from an open cup. Caregivers may need to provide foods or liquids so that self-feeding is possible, or they may need to feed the person with A–T. In general, meals should be completed within approximately 30 minutes. Longer meals may be stressful, interfere with other daily activities, and limit the intake of necessary liquids and nutrients. If swallowing problems (dysphagia) occur, they typically present during the second decade of life. Dysphagia is common because of the neurological changes that interfere with coordination of mouth and pharynx (throat) movements that are needed for safe and efficient swallowing. Coordination problems involving the mouth may make chewing difficult and increase the duration of meals. Problems involving the pharynx may cause liquid, food, and saliva to be inhaled into the airway (aspiration). People with dysphagia may not cough when they aspirate (silent aspiration). Swallowing problems and especially swallowing problems with silent aspiration may cause lung problems due to inability to cough and clear food and liquids from the airway. Warning signs of a swallowing problem Choking or coughing when eating or drinking Poor weight gain (during ages of expected growth) or weight loss at any age Excessive drooling Mealtimes longer than 40 – 45 minutes, on a regular basis Foods or drinks previously enjoyed are now refused or difficult Chewing problems Increase in the frequency or duration of breathing or respiratory problems Increase in lung infections Eye and vision Most people develop telangiectasia (prominent blood vessels) in the membrane that covers the white part (sclera) of the eye. Vision (ability to see objects in focus) is normal. Control of eye movement is often impaired, affecting visual functions that require fast, accurate eye movements from point to point (e.g. reading). Eye misalignments (strabismus) are common, but may be treatable. There may be difficulty in coordinating eye position and shaping the lens to see objects up close. Orthopedics Many individuals with A–T develop deformities of the feet that compound the difficulty they have with walking due to impaired coordination. Early treatment may slow progression of this deformity. Bracing or surgical correction sometimes improves stability at the ankle sufficient to enable an individual to walk with support, or bear weight during assisted standing transfers from one seat to another. Severe scoliosis is relatively uncommon, but probably does occur more often than in those without A–T. Spinal fusion is only rarely indicated. Genetics A–T is caused by mutations in the ATM (ATM serine/threonine kinase or ataxia–telangiectasia mutated) gene, which was cloned in 1995. ATM is located on human chromosome 11 (11q22.3) and is made up of 69 exons spread across 150kb of genomic DNA. The mode of inheritance for A–T is autosomal recessive. Each parent is a carrier, meaning that they have one normal copy of the A–T gene (ATM) and one copy which is mutated. A–T occurs if a child inherits the mutated A–T gene from each parent, so in a family with two carrier parents, there is 1 chance in 4 that a child born to the parents will have the disorder. Prenatal diagnosis (and carrier detection) can be carried out in families if the errors (mutation) in an affected child's two ATM genes have been identified. The process of getting this done can be complicated and, as it requires time, should be arranged before conception. Looking for mutations in the ATM gene of an unrelated person (for example, the spouse of a known A–T carrier) presents significant challenges. Genes often have variant spellings (polymorphisms) which do not affect function. In a gene as large as ATM, such variant spellings are likely to occur and doctors cannot always predict whether a specific variant will or will not cause disease. Genetic counseling can help family members of an A–T patient understand what can or cannot be tested, and how the test results should be interpreted. Carriers of A–T, such as the parents of a person with A–T, have one mutated copy of the ATM gene and one normal copy. They are generally healthy, but there is an increased risk of breast cancer in women. This finding has been confirmed in a variety of different ways, and is the subject of current research. Standard surveillance (including monthly breast self-exams and mammography at the usual schedule for age) is recommended, unless additional tests are indicated because the individual has other risk factors (e.g., family history of breast cancer). Pathophysiology How does loss of the ATM protein create a multisystem disorder? A–T has been described as a genome instability syndrome, a DNA repair disorder and a DNA damage response (DDR) syndrome. ATM, the gene responsible for this multi-system disorder, encodes a protein of the same name which coordinates the cellular response to DNA double strand breaks (DSBs). Radiation therapy, chemotherapy that acts like radiation (radiomimetic drugs) and certain biochemical processes and metabolites can cause DSBs. When these breaks occur, ATM stops the cell from making new DNA (cell cycle arrest) and recruits and activates other proteins to repair the damage. Thus, ATM allows the cell to repair its DNA before the completion of cell division. If DNA damage is too severe, ATM will mediate the process of programmed cell death (apoptosis) to eliminate the cell and prevent genomic instability. Cancer and radiosensitivity In the absence of the ATM protein, cell-cycle check-point regulation and programmed cell death in response to DSBs are defective. The result is genomic instability which can lead to the development of cancers. Irradiation and radiomimetic compounds induce DSBs which are unable to be repaired appropriately when ATM is absent. Consequently, such agents can prove especially cytotoxic to A–T cells and people with A–T. Delayed pubertal development (gonadal dysgenesis) Infertility is often described as a characteristic of A–T. Whereas this is certainly the case for the mouse model of A–T, in humans it may be more accurate to characterize the reproductive abnormality as gonadal atrophy or dysgenesis characterized by delayed pubertal development. Because programmed DSBs are generated to initiate genetic recombinations involved in the production of sperm and eggs in reproductive organs (a process known as meiosis), meiotic defects and arrest can occur when ATM is not present. Immune system defects and immune-related cancers As lymphocytes develop from stem cells in the bone marrow into mature lymphocytes in the periphery, they rearrange special segments of their DNA [V(D)J recombination process]. This process requires them to make DSBs, which are difficult to repair in the absence of ATM. As a result, most people with A–T have reduced numbers of lymphocytes and some impairment of lymphocyte function (such as an impaired ability to make antibodies in response to vaccines or infections). In addition, broken pieces of DNA in chromosomes involved in the above-mentioned rearrangements have a tendency to recombine with other genes (translocation), making the cells prone to the development of cancer (lymphoma and leukemia). Progeric changes Cells from people with A–T demonstrate genomic instability, slow growth and premature senescence in culture, shortened telomeres and an ongoing, low-level stress response. These factors may contribute to the progeric (signs of early aging) changes of skin and hair sometimes observed in people with A–T. For example, DNA damage and genomic instability cause melanocyte stem cell (MSC) differentiation which produces graying. Thus, ATM may be a “stemness checkpoint” protecting against MSC differentiation and premature graying of the hair. Telangiectasia The cause of telangiectasia or dilated blood vessels in the absence of the ATM protein is not yet known. Increased alpha-fetoprotein (AFP) levels Approximately 95% of people with A–T have elevated serum AFP levels after the age of two, and measured levels of AFP appear to increase slowly over time. AFP levels are very high in the newborn, and normally descend to adult levels over the first year to 18 months. The reason for why individuals with A–T have elevated levels of AFP is not yet known. Neurodegeneration A–T is one of several DNA repair disorders which result in neurological abnormalities or degeneration. Arguably some of the most devastating symptoms of A–T are a result of progressive cerebellar degeneration, characterized by the loss of Purkinje cells and, to a lesser extent, granule cells (located exclusively in the cerebellum). The cause of this cell loss is not known, though many hypotheses have been proposed based on experiments performed both in cell culture and in the mouse model of A–T. Current hypotheses explaining the neurodegeneration associated with A–T include the following: Defective DNA damage response in neurons which can lead to Failed clearance of genomically damaged neurons during development Transcription stress and abortive transcription including topoisomerase 1 cleavage complex (TOP1cc) dependent lesions Aneuploidy Defective response to oxidative stress characterized by elevated ROS and altered cellular metabolism Mitochondrial dysfunction Defects in neuronal function: Inappropriate cell cycle re-entry of post-mitotic (mature) neurons Synaptic/vesicular dysregulation HDAC4 dysregulation Histone hypermethylation and altered epigenetics Altered protein turnover These hypotheses may not be mutually exclusive and more than one of these mechanisms may underlie neuronal cell death when there is an absence or deficiency of ATM. Further, cerebellar damage and loss of Purkinje and granule cells do not explain all of the neurologic abnormalities seen in people with A–T. The effects of ATM deficiency on the other areas of the brain outside of the cerebellum are being actively investigated. Radiation exposure People with A–T have an increased sensitivity to ionizing radiation (X-rays and gamma rays). Therefore, X-ray exposure should be limited to times when it is medically necessary, as exposing an A–T patient to ionizing radiation can damage cells in such a way that the body cannot repair them. The cells can cope normally with other forms of radiation, such as ultraviolet light, so there is no need for special precautions from sunlight exposure. Diagnosis The diagnosis of A–T is usually suspected by the combination of neurologic clinical features (ataxia, abnormal control of eye movement, and postural instability) with telangiectasia and sometimes increased infections, and confirmed by specific laboratory abnormalities (elevated alpha-fetoprotein levels, increased chromosomal breakage or cell death of white blood cells after exposure to X-rays, absence of ATM protein in white blood cells, or mutations in each of the person's ATM genes). A variety of laboratory abnormalities occur in most people with A–T, allowing for a tentative diagnosis to be made in the presence of typical clinical features. Not all abnormalities are seen in all patients. These abnormalities include: Elevated and slowly increasing alpha-fetoprotein levels in serum after 2 years of age Immunodeficiency with low levels of immunoglobulins (especially IgA, IgG subclasses, and IgE) and low number of lymphocytes in the blood Chromosomal instability (broken pieces of chromosomes) Increased sensitivity of cells to x-ray exposure (cells die or develop even more breaks and other damage to chromosomes) Cerebellar atrophy on MRI scan The diagnosis can be confirmed in the laboratory by finding an absence or deficiency of the ATM protein in cultured blood cells, an absence or deficiency of ATM function (kinase assay), or mutations in both copies of the cell's ATM gene. These more specialized tests are not always needed, but are particularly helpful if a child's symptoms are atypical. Differential diagnosis There are several other disorders with similar symptoms or laboratory features that physicians may consider when diagnosing A–T. The three most common disorders that are sometimes confused with A–T are: Cerebral palsy Friedreich's ataxia Cogan oculomotor apraxia Each of these can be distinguished from A–T by the neurologic exam and clinical history. Cerebral palsy (CP) describes a non-progressive disorder of motor function stemming from malformation or early damage to the brain. CP can manifest in many ways, given the different manner in which brain can be damaged; in common to all forms is the emergence of signs and symptoms of impairment as the child develops. However, milestones that have been accomplished and neurologic functions that have developed do not deteriorate in CP as they often do in children with A–T in the late pre-school years. Most children with ataxia caused by CP do not begin to walk at a normal age, whereas most children with A–T start to walk at a normal age even though they often "wobble" from the start. Pure ataxia is a rare manifestation of early brain damage or malformation, however, and the possibility of an occult genetic disorder of brain should be considered and sought for those in whom ataxia is the chief manif estation of CP. Children with ataxic CP will not manifest the laboratory abnormalities associated with A–T. Cogan occulomotor apraxia is a rare disorder of development. Affected children have difficulty moving their eyes only to a new visual target, so they will turn their head past the target to “drag” the eyes to the new object of interest, then turn the head back. This tendency becomes evident in late infancy and toddler years, and mostly improves with time. This contrasts to the oculomotor difficulties evident in children with A–T, which are not evident in early childhood but emerge over time. Cogan's oculomotor apraxia is generally an isolated problem, or may be associated with broader developmental delay. Friedreich ataxia (FA) is the most common genetic cause of ataxia in children. Like A–T, FA is a recessive disease, appearing in families without a history of the disorder. FA is caused by mutation in the frataxin gene, most often an expansion of a naturally occurring repetition of the three nucleotide bases GAA from the usual 5–33 repetitions of this trinucleotide sequence to greater than 65 repeats on each chromosome. Most often the ataxia appears between 10 and 15 years of age, and differs from A–T by the absence of telangiectasia and oculomotor apraxia, a normal alpha fetalprotein, and the frequent presence of scoliosis, absent tendon reflexes, and abnormal features on the EKG. Individuals with FA manifest difficulty standing in one place that is much enhanced by closure of the eyes (Romberg sign) that is not so apparent in those with A–T – even though those with A–T may have greater difficulty standing in one place with their eyes open. There are other rare disorders that can be confused with A–T, either because of similar clinical features, a similarity of some laboratory features, or both. These include: Ataxia–oculomotor apraxia type 1 (AOA1) Ataxia–oculomotor apraxia type 2 (AOA2 also known as SCAR1) Ataxia–telangiectasia like disorder (ATLD) Nijmegen breakage syndrome (NBS) Ataxia–oculomotor apraxia type 1 (AOA1) is an autosomal recessive disorder similar to A–T in manifesting increasing problems with coordination and oculomotor apraxia, often at a similar age to those having A–T. It is caused by mutation in the gene coding for the protein aprataxin. Affected individuals differ from those with A–T by the early appearance of peripheral neuropathy, early in their course manifest difficulty with initiation of gaze shifts, and the absence of ocular telangiectasia, but laboratory features are of key importance in the differentiation of the two. Individuals with AOA1 have a normal AFP, normal measures of immune function, and after 10–15 years have low serum levels of albumin. Genetic testing of the aprataxin gene can confirm the diagnosis. There is no enhanced risk for cancer. Ataxia–oculomotor apraxia type 2 (AOA2) is an autosomal recessive disorder also similar to A–T in manifesting increasing problems with coordination and peripheral neuropathy, but oculomotor apraxia is present in only half of affected individuals. Ocular telangiectasia do not develop. Laboratory abnormalities of AOA2 are like A–T, and unlike AOA1, in having an elevated serum AFP level, but like AOA1 and unlike A–T in having normal markers of immune function. Genetic testing of the senataxin gene (SETX) can confirm the diagnosis. There is no enhanced risk for cancer. Ataxia–telangiectasia like disorder (ATLD) is an extremely rare condition, caused by mutation in the hMre11 gene, that could be considered in the differential diagnosis of A–T. Patients with ATLD are very similar to those with A–T in showing a progressive cerebellar ataxia, hypersensitivity to ionizing radiation and genomic instability. Those rare individuals with ATLD who are well described differ from those with A–T by the absence of telangiectasia, normal immunoglobulin levels, a later onset, and a slower progression of the symptoms. Because of its rarity, it is not yet known whether or not ATLD carries an increased risk to develop cancer. Because those mutations of Mre11 that severely impair the MRE11 protein are incompatible with life, individuals with ATLD all have some partial function of the Mre11 protein, and hence likely all have their own levels of disease severity. Nijmegen breakage syndrome (NBS) is a rare genetic disorder that has similar chromosomal instability to that seen in people with A–T, but the problems experienced are quite different. Children with NBS have significant microcephaly, a distinct facial appearance, short stature, and moderate cognitive impairment, but do not experience any neurologic deterioration over time. Like those with A–T, children with NBS have enhanced sensitivity to radiation, disposition to lymphoma and leukemia, and some laboratory measures of impaired immune function, but do not have ocular telangiectasia or an elevated level of AFP. The proteins expressed by the hMre11 (defective in ATLD) and Nbs1 (defective in NBS) genes exist in the cell as a complex, along with a third protein expressed by the hRad50 gene. This complex, known as the MRN complex, plays an important role in DNA damage repair and signaling and is required to recruit ATM to the sites of DNA double strand breaks. Mre11 and Nbs1 are also targets for phosphorylation by the ATM kinase. Thus, the similarity of the three diseases can be explained in part by the fact that the protein products of the three genes mutated in these disorders interact in common pathways in the cell. Differentiation of these disorders is often possible with clinical features and selected laboratory tests. In cases where the distinction is unclear, clinical laboratories can identify genetic abnormalities of ATM, aprataxin and senataxin, and specialty centers can identify abnormality of the proteins of potentially responsible genes, such as ATM, MRE11, nibrin, TDP1, aprataxin and senataxin as well as other proteins important to ATM function such as ATR, DNA-PK, and RAD50. Management Ataxia and other neurologic problems There is no treatment known to slow or stop the progression of the neurologic problems. Treatment of A–T is symptomatic and supportive. Physical, occupational and speech therapies and exercise may help maintain function but will not slow the course of neurodegeneration. Therapeutic exercises should not be used to the point of fatigue and should not interfere with activities of daily life. Certain anti-Parkinson and anti-epileptic drugs may be useful in the management of symptoms, but should be prescribed in consultation with a neurologist. Immune problems All individuals with A–T should have at least one comprehensive immunologic evaluation that measures the number and type of lymphocytes in the blood (T-lymphocytes and B-lymphocytes), the levels of serum immunoglobulins (IgG, IgA, and IgM) and antibody responses to T-dependent (e.g., tetanus, Hemophilus influenzae b) and T-independent (23-valent pneumococcal polysaccharide) vaccines. For the most part, the pattern of immunodeficiency seen in an A–T patient early in life (by age five) will be the same pattern seen throughout the lifetime of that individual. Therefore, the tests need not be repeated unless that individual develops more problems with infection. Problems with immunity sometimes can be overcome by immunization. Vaccines against common bacterial respiratory pathogens such as Hemophilus influenzae, pneumococci and influenza virus (the “flu”) are commercially available and often help to boost antibody responses, even in individuals with low immunoglobulin levels. If the vaccines do not work and the patient continues to have problems with infections, gamma globulin therapy (IV or subcutaneous infusions of antibodies collected from normal individuals) may be of benefit. A small number of people with A–T develop an abnormality in which one or more types of immunoglobulin are increased far beyond the normal range. In a few cases, the immunoglobulin levels can be increased so much that the blood becomes thick and does not flow properly. Therapy for this problem must be tailored to the specific abnormality found and its severity. If an individual patient's susceptibility to infection increases, it is important to reassess immune function in case deterioration has occurred and a new therapy is indicated. If infections are occurring in the lung, it is also important to investigate the possibility of dysfunctional swallow with aspiration into the lungs (see above sections under Symptoms: Lung Disease and Symptoms: Feeding, Swallowing and Nutrition.) Most people with A–T have low lymphocyte counts in the blood. This problem seems to be relatively stable with age, but a rare number of people do have progressively decreasing lymphocyte counts as they get older. In the general population, very low lymphocyte counts are associated with an increased risk for infection. Such individuals develop complications from live viral vaccines (measles, mumps, rubella and chickenpox), chronic or severe viral infections, yeast infections of the skin and vagina, and opportunistic infections (such as pneumocystis pneumonia). Although lymphocyte counts are often as low in people with A–T, they seldom have problems with opportunistic infections. (The one exception to that rule is that problems with chronic or recurrent warts are common.) The number and function of T-lymphocytes should be re-evaluated if a person with A–T is treated with corticosteroid drugs such as prednisone for longer than a few weeks or is treated with chemotherapy for cancer. If lymphocyte counts are low in people taking those types of drugs, the use of prophylactic antibiotics is recommended to prevent opportunistic infections. If the tests show significant abnormalities of the immune system, a specialist in immunodeficiency or infectious diseases will be able to discuss various treatment options. Absence of immunoglobulin or antibody responses to vaccine can be treated with replacement gamma globulin infusions, or can be managed with prophylactic antibiotics and minimized exposure to infection. If antibody function is normal, all routine childhood immunizations including live viral vaccines (measles, mumps, rubella and varicella) should be given. In addition, several “special” vaccines (that is, licensed but not routine for otherwise healthy children and young adults) should be given to decrease the risk that an A–T patient will develop lung infections. The patient and all household members should receive the influenza (flu) vaccine every fall. People with A–T who are less than two years old should receive three (3) doses of a pneumococcal conjugate vaccine (Prevnar) given at two month intervals. People older than two years who have not previously been immunized with Prevnar should receive two (2) doses of Prevnar. At least 6 months after the last Prevnar has been given and after the child is at least two years old, the 23-valent pneumococcal vaccine should be administered. Immunization with the 23-valent pneumococcal vaccine should be repeated approximately every five years after the first dose. In people with A–T who have low levels of IgA, further testing should be performed to determine whether the IgA level is low or completely absent. If absent, there is a slightly increased risk of a transfusion reaction. “Medical Alert” bracelets are not necessary, but the family and primary physician should be aware that if there is elective surgery requiring red cell transfusion, the cells should be washed to decrease the risk of an allergic reaction. People with A–T also have an increased risk of developing autoimmune or chronic inflammatory diseases. This risk is probably a secondary effect of their immunodeficiency and not a direct effect of the lack of ATM protein. The most common examples of such disorders in A–T include immune thrombocytopenia (ITP), several forms of arthritis, and vitiligo. Lung disease Recurrent sinus and lung infections can lead to the development of chronic lung disease. Such infections should be treated with appropriate antibiotics to prevent and limit lung injury. Administration of antibiotics should be considered when children and adults have prolonged respiratory symptoms (greater than 7 days), even following what was presumed to have been a viral infection. To help prevent respiratory illnesses from common respiratory pathogens, annual influenza vaccinations should be given and pneumococcal vaccines should be administered when appropriate. Antibiotic treatment should also be considered in children with chronic coughs that are productive of mucous, those who do not respond to aggressive pulmonary clearance techniques and in children with muco-purulent secretions from the sinuses or chest. A wet cough can also be associated with chronic aspiration which should be ruled out through proper diagnostic studies, however aspiration and respiratory infections are not necessarily exclusive of each other. In children and adults with bronchiectasis, chronic antibiotic therapy should be considered to slow chronic lung disease progression. Culturing of the sinuses may be needed to direct antibiotic therapy. This can be done by an Ear Nose and Throat (ENT) specialist. In addition, diagnostic bronchoscopy may be necessary in people who have recurrent pneumonias, especially those who do not respond or respond incompletely to a course of antibiotics. Clearance of bronchial secretions is essential for good pulmonary health and can help limit injury from acute and chronic lung infections. Children and adults with increased bronchial secretions can benefit from routine chest therapy using the manual method, an a cappella device or a chest physiotherapy vest. Chest physiotherapy can help bring up mucous from the lower bronchial tree, however an adequate cough is needed to remove secretions. In people who have decreased lung reserve and a weak cough, use of an insufflator-exsufflator (cough-assist) device may be useful as a maintenance therapy or during acute respiratory illnesses to help remove bronchial secretions from the upper airways. Evaluation by a Pulmonology specialist however, should first be done to properly assess patient suitability. Children and adults with chronic dry cough, increased work of breathing (fast respiratory rate, shortness of breath at rest or with activities) and absence of an infectious process to explain respiratory symptoms should be evaluated for interstitial lung disease or another intrapulmonary process. Evaluation by a Pulmonologist and a CT scan of the chest should be considered in individuals with symptoms of interstitial lung disease or to rule other non-infectious pulmonary processes. People diagnosed with interstitial lung disease may benefit from systemic steroids. Feeding, swallowing and nutrition Oral intake may be aided by teaching persons with A–T how to drink, chew and swallow more safely. The propriety of treatments for swallowing problems should be determined following evaluation by an expert in the field of speech-language pathology. Dieticians may help treat nutrition problems by recommending dietary modifications, including high calorie foods or food supplements. A feeding (gastrostomy) tube is recommended when any of the following occur: A child cannot eat enough to grow or a person of any age cannot eat enough to maintain weight; Aspiration is problematic; Mealtimes are stressful or too long, interfering with other activities. Feeding tubes can decrease the risk of aspiration by enabling persons to avoid liquids or foods that are difficult to swallow and provide adequate calories without the stress and time commitment of prolonged meals. Gastrostomy tubes do not prevent people from eating by mouth. Once a tube is in place, the general goal should be to maintain weight at the 10–25th percentile. Education and socialization Most children with A–T have difficulty in school because of a delay in response time to visual, verbal or other cues, slurred and quiet speech (dysarthria), abnormalities of eye control (oculomotor apraxia), and impaired fine motor control. Despite these problems, children with A–T often enjoy school if proper accommodations to their disability can be made. The decision about the need for special education classes or extra help in regular classes is highly influenced by the local resources available. Decisions about proper educational placement should be revisited as often as circumstances warrant. Despite their many neurologic impairments, most individuals with A–T are very socially aware and socially skilled, and thus benefit from sustained peer relationships developed at school. Some individuals are able to function quite well despite their disabilities and a few have graduated from community colleges. Many of the problems encountered will benefit from special attention, as problems are often related more to “input and output” issues than to intellectual impairment. Problems with eye movement control make it difficult for people with A–T to read, yet most fully understand the meaning and nuances of text that is read to them. Delays in speech initiation and lack of facial expression make it seem that they do not know the answers to questions. Reduction of the skilled effort needed to answer questions, and an increase of the time available to respond, is often rewarded by real accomplishment. It is important to recognize that intellectual disability is not regularly a part of the clinical picture of A–T although school performance may be suboptimal because of the many difficulties in reading, writing, and speech. Children with A–T are often very conscious of their appearance, and strive to appear normal to their peers and teachers. Life within the ataxic body can be tiring. The enhanced effort needed to maintain appearances and increased energy expended in abnormal tone and extra movements all contribute to physical and mental fatigue. As a consequence, for some a shortened school day yields real benefits. General recommendations All children with A–T need special attention to the barriers they experience in school. In the United States, this takes the form of a formal IEP (Individualized Education Program). Children with A–T tend to be excellent problem solvers. Their involvement in how to best perform tasks should be encouraged. Speech-language pathologists may facilitate communication skills that enable persons with A–T to get their messages across (using key words vs. complete sentences) and teach strategies to decrease frustration associated with the increase time needed to respond to questions (e.g., holding up a hand and informing others about the need to allow more time for responses). Rarely helpful are traditional speech therapies that focus on the production of specific sounds and strengthening of the lip and tongue muscles. Classroom aides may be appropriate, especially to help with scribing, transportation through the school, mealtimes and toileting. The impact of an aide on peer relationships should be monitored carefully. Physical therapy is useful to maintain strength and general cardiovascular health. Horseback therapy and exercises in a swimming pool are often well tolerated and fun for people with A–T. However, no amount of practice will slow the cerebellar degeneration or improve neurologic function. Exercise to the point of exhaustion should be avoided. Hearing is normal throughout life. Books on tape may be a useful adjunct to traditional school materials. Early use of computers (preschool) with word completion software should be encouraged. Practicing coordination (e.g. balance beam or cursive writing exercises) is not helpful. Occupational therapy is helpful for managing daily living skills. Allow rest time, shortened days, reduced class schedule, reduced homework, modified tests as necessary. Like all children, those with A–T need to have goals to experience the satisfaction of making progress. Social interactions with peers are important, and should be taken into consideration for class placement. For everyone long-term peer relationships can be the most rewarding part of life; for those with A–T establishing these connections in school years can be helpful. Treatment No curative medication has been approved for the treatment of inherited cerebellar ataxias, including Ataxia-Telangiectasia. The treatment of A-T remains based in medical management (of immunodeficiencies and sinopulmonary infections, neurologic dysfunction, and malignancy) and neurorehabilitation (physical, occupational, and speech/swallowing therapy; adaptive equipment; and nutritional counseling). N-Acetyl-Leucine N-Acetyl-Leucine is an orally administered, modified amino acid that is being developed as a novel treatment for multiple rare and common neurological disorders by IntraBio Inc (Oxford, United Kingdom). N-Acetyl-Leucine has been granted multiple orphan drug designations from the U.S. Food & Drug Administration (FDA)and the European Medicines Agency (EMA)for the treatment of various genetic diseases, including Ataxia-Telangiectasia. N-Acetyl-Leucine has also been granted Orphan Drug Designations in the US and EU for related inherited cerebellar ataxias, such as Spinocerebellar Ataxias. U.S. Food & Drug Administration (FDA) and the European Medicines Agency (EMA). Published case series studies have demonstrated the positive clinical benefit of treatment with N-Acetyl-Leucine various inherited cerebellar ataxias. Additional compassionate use studies in patients with Ataxia Telangiectasia have shown the symptomatic, and disease-modifying potential of the treatment. These studies further demonstrated that the treatment is well tolerated, with a good safety profile. A multinational clinical trial investigating N-Acetyl-L-Leucine for the treatment Ataxia-Telangiectasia began in 2019. IntraBio is also conducting two parallel clinical trials with N-Acetyl-L-Leucine for the treatment Niemann-Pick disease type C and GM2 Gangliosidosis (Tay-Sachs and Sandhoff Disease) Future opportunities to develop N-Acetyl-Leucine include Lewy Body Dementia, Amyotrophic lateral sclerosis, Restless Leg Syndrome, Multiple Sclerosis, and Migraine. Prognosis The life expectancy of people with A–T is highly variable. The average is approximately 25 years, but continues to improve with advances in care. The two most common causes of death are chronic lung disease (about one-third of cases) and cancer (about one-third of cases). Epidemiology Individuals of all races and ethnicities are affected equally. The incidence worldwide is estimated to be between 1 in 40,000 and 1 in 100,000 people. Research directions An open-label Phase II clinical trial studying the use of red blood cells (erythrocytes) loaded with dexamethasone sodium phosphate found that this treatment improved symptoms and appeared to be well tolerated. This treatment uses a unique delivery system for medication by using the patient's own red blood cells as the delivery vehicle for the drug. Given the other immunologic deficits present in individuals with A–T, there remains a need to evaluate the therapeutic potential of steroids further, particularly with respect to the duration of any benefit and its long-term safety. References External links About A–T from the NINDS Orphanet for A–T GeneReviews for ataxia–telangiectasia Replication-Independent Double-Strand Breaks (DSBs) Discusses importance of the ATM kinase Category:Chromosome instability syndromes Category:Genodermatoses Category:Systemic atrophies primarily affecting the central nervous system Category:Neurodegenerative disorders Category:IUIS-PID table 3 immunodeficiencies Category:DNA replication and repair-deficiency disorders Category:Syndromes affecting the nervous system Category:Syndromes with tumors	3.46875	3	[ 0.004180908203125, -0.010009765625, 0.0185546875, 0.0244140625, 0.00927734375, -0.0166015625, 0.02197265625, -0.005523681640625, -0.003387451171875, 0.0301513671875, -0.00897216796875, -0.0068359375, 0.01251220703125, 0.006561279296875, -0.032470703125, -0.012939453125, -0.0145263671875, 0.01287841796875, 0.007049560546875, 0.004425048828125, 0.033935546875, -0.004241943359375, -0.01190185546875, -0.01141357421875, 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Ripples in spacetime: Science's 2016 Breakthrough of the Year The discovery of ripples in spacetime—gravitational waves—shook the scientific world this year. It fulfilled a prediction made 100 years ago by Albert Einstein and capped a 40-year quest to spot the infinitesimal ripples. But instead of the end of the story, scientists see the discovery as the birth of a new field: gravitational wave astronomy. In 1915, Einstein explained that gravity arises because massive bodies warp space and time, or spacetime, causing free- falling objects to follow curved paths such as the arc of a thrown ball or the elliptical orbit of a planet around its sun. Einstein then calculated that a barbell-shaped distribution of mass whirling end-to-end like a baton should radiate ripples in spacetime that zip along at light speed—gravitational waves. On 11 February, physicists working with the Laser Interferometer Gravitational-Wave Observatory (LIGO)—twin instruments in Hanford, Washington, and Livingston, Louisiana—announced that they had seen just what Einstein predicted: a burst of waves created as two black holes spiraled into each other 1.3 billion light- years away. The triumph was hard earned. Einstein himself vacillated for decades over whether gravitational waves should exist. Even if they did, the only source Einstein could imagine, two orbiting stars, would produce waves too feeble to detect. By the late 1960s, however, astrophysicists knew of much denser concentrations of mass. They had spotted neutron stars and dreamed up black holes, the ultraintense gravitational fields left behind when massive stars collapse to nothing. Spiraling together, such things could, in theory, produce observable waves. In 1972, Rainer Weiss, a physicist at the Massachusetts Institute of Technology in Cambridge, set out a scheme to detect them with L-shaped optical instruments called interferometers, sowing the seed for LIGO. People’s choice Visitors to Science’s website were offered the chance to vote on a list of candidates for Breakthrough of the Year while Science editors and writers were finalizing their choices. A first round of voting narrowed the top candidates to five, and a second round, in which some 225,000 votes were cast, determined the final People’s Choice. In the end, a breakthrough in culture techniques that enabled researchers to keep human embryos developing in the lab for almost 2 weeks edged out Science’s top choice, the detection of gravitational waves. The full results: Human embryo culture 43% Gravitational waves 32% Portable DNA sequencers 13% AI beats Go champ 7% Worn-out cells and aging 5% The discovery of ripples in spacetime—gravitational waves—shook the scientific world this year. It fulfilled a prediction made 100 years ago by Albert Einstein and capped a 40-year quest to spot the infinitesimal ripples. But instead of the end of the story, scientists see the discovery as the birth of a new field: gravitational wave astronomy. In 1915, Einstein explained that gravity arises because massive bodies warp space and time, or spacetime, causing free- falling objects to follow curved paths such as the arc of a thrown ball or the elliptical orbit of a planet around its sun. Einstein then calculated that a barbell-shaped distribution of mass whirling end-to-end like a baton should radiate ripples in spacetime that zip along at light speed—gravitational waves. On 11 February, physicists working with the Laser Interferometer Gravitational-Wave Observatory (LIGO)—twin instruments in Hanford, Washington, and Livingston, Louisiana—announced that they had seen just what Einstein predicted: a burst of waves created as two black holes spiraled into each other 1.3 billion light- years away. The triumph was hard earned. Einstein himself vacillated for decades over whether gravitational waves should exist. Even if they did, the only source Einstein could imagine, two orbiting stars, would produce waves too feeble to detect. By the late 1960s, however, astrophysicists knew of much denser concentrations of mass. They had spotted neutron stars and dreamed up black holes, the ultraintense gravitational fields left behind when massive stars collapse to nothing. Spiraling together, such things could, in theory, produce observable waves. In 1972, Rainer Weiss, a physicist at the Massachusetts Institute of Technology in Cambridge, set out a scheme to detect them with L-shaped optical instruments called interferometers, sowing the seed for LIGO. Each LIGO interferometer has two 4- kilometer-long arms with mirrors at either end, housed in a giant vacuum chamber. By bouncing laser light between the mirrors, physicists can compare the arms’ lengths to within 1/10,000 the width of a proton. A passing gravitational wave would generally stretch the arms by different amounts, and that’s what the LIGO team spotted. The tight fit between that first signal and computer modeling validated Einstein’s theory of gravity, known as general relativity, as never before. Now, physicists are eagerly anticipating what may come next, because gravitational waves promise an entirely new way to peer into the cosmos. First, physicists hope to spot many more events. LIGO already has detected a second black hole merger and a third, weaker signal. The interferometers resumed taking data last month, and if they can reach their design sensitivity, they may eventually see a black hole merger on average once a day. Other instruments will soon join the hunt. The upgraded VIRGO detector in Italy should turn on early next year. Physicists in Japan are building a detector called the Kamioka Gravitational Wave Detector, and LIGO physicists plan to add a detector in India in the early 2020s. Three or more detectors together should be able to pinpoint a source in the sky by triangulation. That could help telescopes home in on the same event, and perhaps detect other signals from it. For example, if gravitational wave detectors sense the merger of two neutron stars and telescopes pick up light or x-rays from it, the signals together might offer clues about the exotic matter in neutron stars. The detectors might even test wilder ideas about black holes. Quantum theory suggests a black hole might contain a hidden “firewall” that would obliterate anything that falls in. If so, merging black holes should produce gravitational wave echoes, some theorists predict. Others speculate that a spinning black hole could generate a cloud of hypothetical particles called axions, which could generate gravitational waves by annihilating one another en masse. Meanwhile, some astronomers are trying to detect gravitational waves in a different way. Within the hearts of large galaxies lurk supermassive black holes weighing hundreds of millions or billions of solar masses. When two such monsters merge, they radiate hugely powerful waves with wavelengths light-years long—thousands of times longer than instruments like LIGO can detect. To spot those waves, astronomers are turning to stellar timepieces called millisecond pulsars. Pulsars—spinning neutron stars—emit incredibly regular pulses of radio waves. As long-wavelength gravitational waves buffet Earth, they should push the planet toward some pulsars and away from others. That motion would, in turn, shorten or stretch the time between pulses from pulsars in different directions, in an effect akin to the Doppler shift. The resulting variations and correlations among pulsars’ timing should reveal the cacophony of long-wavelength gravitational waves, and the spectrum of longer and shorter waves would help physicists trace the rate at which galaxies formed and merged throughout cosmic history. Teams in the United States, Europe, and Australia hope to see a signal within 2 or 3 years— although the U.S. effort is threatened by plans at the National Science Foundation to defund the two radio telescopes it uses.	3.765625	4	[ -0.000518798828125, -0.006988525390625, -0.00007104873657226562, -0.00043487548828125, -0.006866455078125, -0.01495361328125, -0.0220947265625, 0.01092529296875, -0.00927734375, -0.033447265625, -0.004730224609375, -0.01300048828125, 0.0137939453125, 0.00244140625, -0.00439453125, -0.013427734375, -0.01470947265625, 0.01458740234375, 0.00016689300537109375, 0.0203857421875, 0.01611328125, 0.00135040283203125, -0.000476837158203125, -0.015625, -0.01165771484375, -0.007080078125, 0.0125732421875, -0.012451171875, 0.004730224609375, -0.00799560546875, 0.01068115234375, 0.0030517578125, -0.02197265625, -0.007476806640625, 0.004425048828125, 0.01513671875, 0.012939453125, 0.01239013671875, -0.015380859375, 0.00164031982421875, -0.01470947265625, 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Artificial Intelligence has already become an essential part of our lives. Several sectors like Politics, Media, and Engineering, etc. are capitalizing all of the capacity of Artificial Intelligence. Hence, we are consuming the services of AI in known or unknown ways. Related Articles Humans created Artificial Intelligence for us to imagine a healthy, secure, connected and creative future ahead. Mechanical Engineering plays a catalyst in the above process of Imagination. In today’s era, education courses are helping us to create people who can bring the distance of Humans and Machines closer. Which can help create new products, systems, and avenues. Let us start from the basic, What is Artificial Intelligence? Artificial Intelligence, well-spoken as A.I is a unit of computer science that works towards creating and building smart appliances/machines which are capable of doing similar or more amount of work than human tendency. Work that requires human intelligence but can be done by Computer Science. A. I simulate and emulate a human’s behavioural pattern through machines. Mechanical Engineering? Mechanical Engineering is a branch of engineering dealing with Design, construction and machines. Within this, a significant area which is related to Artificial Intelligence is Mechanical Design. Mechanical Design comes to be a sub-set for Mechanical Engineering. In Mechanical Engineering Design, we can see the way toward concocting a part, framework or stream to meet desired/needed need. Here, we can see the amalgamation of Science and mathematics. Mechanical Design is a process to design the required component, system, or process, which is necessary to meet the final result. Mechanical Engineering – Mechanical Design and its relation with A.I is majorly used by a Product Design Company. Artificial Intelligence and Mechanical Engineering. The sector of Mechanical Engineering is the primary consumer of Artificial Intelligence as a technology. It is more than any other industry; it is consumed the most in Mechanical designs or engineering works. Sections of Mechanical Engineering like Robotics, Automation, or sensor technology, uses Artificial Intelligence as a technology. So it is easy to say that Mechanical Engineering disseminates the application and use of AI in the eco-system. Benefits of AI for Mechanical Engineering There are different areas where AI impacts the Mechanical Engineering process. The idea behind the work of AI remains the same. It performs activities without humans yet with increased tendency as compared to humans. It is prioritizing the automated part of work, where we feed the computer with data, and as per the command, the machine/process continues its function. We can feel the impact of AI in different areas, such as: Manufacturing Many processes in the manufacturing industry require Mechanical Engineering to be done with components, products, processes, etc. Artificial Intelligence is currently used in similar processes of Mechanical Engineering. Whether in Components, Products, or Processes. It is making sure about its presence being felt. There are many other processes and technologies which are becoming easy – fast and efficient with the help of Artificial Intelligence. Machine’s which can do more work than human tendency and that too with least effort of humans into it is the main goal here. When the above objective is achieved or worked upon, it will send serious implications to different areas of the sector. (And at some places, connections have already started affecting the scenarios) That’s what AI is impacting in the current era for the manufacturing industry. People of the sector are also scared off them losing the jobs. Mechanical Design Whenever we start the process of building a component/product/flow, the first step of it would be of Mechanical Design. Different sectors of services are provided through mechanical Design. To list the few as; Product Design, Machine Design, Mechanical Component Design, Tooling and Fixture Development, Mold Design, Casting Design. All are coming under the umbrella for Mechanical Design Services. A. I. can majorly impact Product Design Services when it comes to designing the concept, examining the product, and also during the manufacturing of the product. Big Data Storage and Usage through IT. Data has proved its presence everywhere. Even the processes and function of Mechanical engineering requires the usage and storage of Data. When it comes to mechanical engineering, the primary area where Data is needed the most is machine learning. Yet another segment of mechanical engineering. Machine learning has changed the perception of the potential of mechanical engineering. It provides better efficiency/flexibility and quality of systems with the help of data, resulting in the improvement of processes and systems in mechanical engineering. It is one of the critical drivers of development for mechanical engineering. Coming back to the discussion of AI’s impact, Artificial Intelligence has a significant role in the increasing trend of Machine Learning. A. I has its comfort zone when it comes to relying on Huge Data and Large Algorithmic learnings. Machine learning, as discussed earlier, is dependent mostly on the constant generation of data and its analysis. A. I learn through those large sets of data and various commands that engineers might have to give in the first place. There are a few other ways where Artificial Intelligence does help during the process of Mechanical Engineering. Such as, Stress Estimation of 3D Structures: Estimating the amount of stress while designing and manufacturing 3D structures. Material Evaluation for different Services: Evaluating materials, its strength – durability – quality and helping in a more exceptional manufacturing process. Structure Generation: While Generating a Structure, AI can help through its algorithms and data storage. It is making the process efficient and transparent. As we discussed, the Impact of AI on mechanical engineering. There are both sides available to Artificial Intelligence: Good and Bad. The Good Ones A. I. can create a negligible amount of error, required that the programming is done in the best possible way. Compared to A. I, Humans have a probability of creating more errors in the work. Compared to Human Speed, it is much faster w.r.t. Work. A. I. lessens the amount of risk attached to the functioning and decision-making process. Through its algorithms and data, it is created to choose only the best possible result. The Bad Ones AI reduces the risk attached to work through its attributes of data and algorithms. But the same process eradicates the Human element attached to the entire process. Resulting in an impact on Moral of the employees. AI lacks creativity. The judgment process of AI is not dynamic, i.e., according to situations. It might not give the best possible output in a condition of Natural Calamity, Disaster, or any on-ground damage. Conclusion Artificial Intelligence isn’t a long listed dream anymore. More and more industries are taking advantage of it and providing some fantastic results that can help human eco-system. Yes, AI might affect an industry’s HR by eradicating the least essential employee. Yes, it might kill the human element attached to the process. Yet, against all of it, it is helping our generation to imagine an entirely new world by impacting the different fields. It is a Superpower. If it is not used with maturity and responsibility, it has all the possibility to backfire us. Remember the Avengers? The post Artificial Intelligence and its Alliance with Mechanical Engineering appeared first on Blog Tesla Outsourcing Services.	3.234375	3	[ 0.0166015625, -0.018798828125, -0.018310546875, 0.0068359375, -0.01373291015625, 0.005126953125, -0.0242919921875, -0.00396728515625, -0.01416015625, -0.0264892578125, 0.0257568359375, -0.000240325927734375, -0.023193359375, 0.003143310546875, -0.00494384765625, -0.0011138916015625, 0.004364013671875, -0.0230712890625, -0.0091552734375, 0.01171875, -0.0045166015625, 0.0274658203125, -0.002960205078125, 0.004791259765625, -0.00506591796875, 0.000041484832763671875, -0.0035247802734375, -0.0038604736328125, 0.013916015625, -0.00469970703125, 0.01300048828125, -0.00225830078125, -0.025146484375, 0.009033203125, 0.0050048828125, 0.00506591796875, 0.004638671875, 0.0108642578125, -0.006011962890625, 0.00927734375, 0.00860595703125, -0.0164794921875, 0.005767822265625, 0.03173828125, -0.00970458984375, -0.01324462890625, -0.022705078125, 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Students work on their own on the Think About It problem. This is a quick problem for students to complete. Students fill in the ratio table. As a class, we discuss why a tape diagram could not be the visual model for this problem. I frame the lesson by telling students that, in this lesson, they will learn a third model that can be used with ratios. Specifically, double number lines are used with part to part rations that have different units. Resources (1) Resources In the Intro to New Material section, students learn to create the double number line model. I guide students to create the double number line for the first example problem. We need to use two number lines because we're representing quantities with different units. I tell students that it would not make sense to model minutes and miles on the same number line. Using these steps, we fill in the notes in this section: Steps for Drawing Double Number lines: Draw two straight parallel lines and label with units and arrow as the end. Draw a tick mark through both lines and label with given ratio. Start with 0 and 0 on each number line. Label the units of each number line. Use skip counting to find equivalent ratios and plot them equidistant from each other. Draw tick marks and label. Stop when the unknown term has been reached. Circle and answer with units. I then guide students through completing the next example in this set. The student sample, from the Independent Practice problem set, shows what student-created double number lines should look like. Resources (2) Resources Students work in pairs for the Partner Practice. As students work, I circulate around the room. I am looking for: Are students correctly labeling the double number lines? Are students correctly drawing the double number line? Equal spacing, numbers that correspond to A are along the same line and B along another line? Are students correctly skip counting to solve the problem. Are students showing clear, logical work? Are students providing an answer to the specific question? Are students checking for the reasonableness of their answer? I'm asking students: What does the ratio mean in this problem? What is the value of each part? How do you know? What is the question asking you to find? How did you know to use a double number line? How did you find the values for the intervals on the double number line? How do you know when to stop skip counting? After 10 minutes of partner work time, the class comes back together. I pull a popsicle stick to cold call on a student. I display one of the double number lines that this student has completed. I cold call another student and ask if the work shown contains a double number line that's constructed correctly. I cold call a third student and ask how the original student knew when to stop the double number line. We discuss problem 2 from this set after work time. I want students using double number lines when the units are different. For problem 2, both parts are measured in rows. Students can use a tape diagram (or ratio table) to solve. It's very likely that students will have used a double number line to represent this problem. Numerically, they will come to the right answer. The conversation after work time will reinforce for students that they should use a double number line for part to part relationships with different units. Otherwise, we'd be able to model the quantities on one number line, if they have the same unit. I then guide students to discuss problem number 4, which involves a total. We discuss the model that would work best here. There will be students who used a double number line, labeling tulips and daisies for each respective number line. They'll have run into the problem of not having a total in the model to work with. Students then independently complete the check for understanding at the end of this section. After 3 minutes of work time, I have students clap out their answer choice for this problem. Resources (1) Resources After 15 minutes of work time, I have students turn and talk with their partners about their responses from problem number 4 in this set. I want students to talk about multiple ways to make sense of this problem. We then discuss problem 7 as a class. I want students to articulate how the differences in the pizza problems led students to model the problems in different ways. Resources (1) Resources I ask students to work with their partners to summarize when a double number line would be the most appropriate visual model. I ask 2-3 pairs to share out their thoughts, and we synthesize the responses into one common understanding: double number lines are used for part to part ratio problems with different units. Resources S Laguda: I think this is a wonderful start in introducing the lesson. Thank you for sharing this. It allows students to work on drawing the double number line, equidistance, etc. I will be using this tomorrow. \| 3 months ago \| Reply	4.4375	4	[ 0.01239013671875, -0.0108642578125, 0.00104522705078125, 0.0034637451171875, 0.00183868408203125, -0.0012969970703125, 0.034912109375, 0.00872802734375, -0.00188446044921875, -0.03662109375, -0.022705078125, 0.006134033203125, -0.003387451171875, 0.0048828125, 0.00689697265625, 0.00750732421875, 0.00061798095703125, 0.01104736328125, -0.0234375, 0.019287109375, 0.00494384765625, 0.009765625, 0.0172119140625, 0.0079345703125, 0.005706787109375, -0.00567626953125, -0.00543212890625, -0.016845703125, 0.011962890625, -0.03173828125, -0.0126953125, 0.01544189453125, -0.00909423828125, -0.00148773193359375, -0.00848388671875, -0.00052642822265625, -0.002044677734375, 0.0291748046875, 0.00848388671875, -0.0230712890625, -0.009765625, 0.00823974609375, 0.01226806640625, 0.0198974609375, 0.0159912109375, -0.01171875, -0.0181884765625, 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Annual fish as a genetic model for aging. Advancement in the genetics of aging and identification of longevity genes has been largely due to the model organisms such as Caenorhabditis elegans and Drosophila melanogaster. However, knowledge gained from these invertebrates will not be able to identify vertebrate-specific longevity genes. The mouse has a relatively long life span of about 3 years, which limits its utility for screening of longevity genes. Fish have been used in aging studies. However, systematic comparison of survivorship curves for fish is lacking. In this study, we compared the survivorship curves of zebrafish and 2 different annual fish, namely, Cynolebias nigripinnis and Nothobranchius rachovii. These studies established that Nothobranchius rachovii has the shortest life span (8.5 months, at which time 10% of population remains). We also established that it is possible to breed Nothobranchius rachovii under laboratory conditions, and showed that their embryos can be stored for several months and hatched at any time by adding water. In addition, we have isolated 31 cDNA markers out of 71 attempted amplifications based on corresponding homologous genomic sequences in zebrafish and Fugu available from public databases, suggesting that approximately 40% of the genes from Nothobranchius rachovii could be easily isolated. Thus, the ability to be bred under laboratory conditions and the availability of cDNA markers for mapping, along with the major advantage of a relatively short life span, make Nothobranchius rachovii an attractive vertebrate genetic model for aging over other available vertebrate models.	3.203125	3	[ -0.000339508056640625, 0.02783203125, 0.01171875, -0.000621795654296875, -0.007720947265625, -0.01434326171875, 0.0159912109375, -0.0076904296875, 0.0123291015625, -0.01019287109375, 0.000537872314453125, 0.0037841796875, -0.01226806640625, 0.0013275146484375, -0.0084228515625, -0.0033721923828125, 0.0081787109375, -0.02587890625, -0.0031280517578125, -0.005615234375, -0.0076904296875, -0.00799560546875, 0.0029144287109375, -0.006256103515625, -0.017333984375, 0.0027618408203125, 0.00994873046875, -0.011474609375, -0.006072998046875, -0.0096435546875, 0.00138092041015625, -0.000640869140625, -0.0186767578125, -0.022216796875, 0.0072021484375, -0.0081787109375, 0.003631591796875, 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With the slow march of the stars to the west each evening and each season, the starry patterns form a celestial calendar. In the northern hemisphere, winter begins on December 21 at 4:44 a.m. CST. At this time the sun’s celestial coordinates are 18 hours of right ascension and -23.5 degrees declination. The sun passes overhead at Tropic of Capricorn, 23.5 degrees south of the equator. On ancient star maps, the sun appeared in front of the stars of Capricornus. Over time the earth has pivoted from the sun’s and moon’s gravitational forces so that the astronomical solstice point appears in front of Sagittarius. See more about this below. The group of stars that signal the beginning of winter is the informal group known as the Winter Triangle that are made of Sirius, Procyon and Sirius. This giant sidereal shape appears complete in the southeastern sky by 9:30 p.m. CST in late December. Sirius, the brightest star in the night sky, is distinctly blue-white through binoculars. It may twinkle vividly when viewed near the horizon on a clear, cold night from heat rising from your terrestrial surroundings. Procyon — known as “Before the Dog” because it rises a little before Sirius, the Dog Star — appears farther north along the eastern horizon. Procyon is not as blue as Sirius. The third corner of the triangle is Betelgeuse, the reddish star at the shoulder or armpit of Orion. Its colors are distinct through binoculars and a small telescope as well. The change of seasons brings us a procession of new celestial signs. The Winter Triangle and other bright stars in the eastern sky tell us that Winter is here. The constellations are represented by multiple definitions. The familiar stick figures made by connecting the stars is the most common fashion. Another way is to divide the sky into patches like those on a quilt, although each is not equal in size. The chart above shows the sun at solstice noon. (The green line represents the sun’s apparent annual path on the sky that is caused by the earth’s revolution. The moon and planets appear to move closely to that line, not on it but within a few degrees. The red line at the top is the celestial equator; it is directly above our planet’s equator in the sky. The vertical white line is the meridian, an imaginary line that starts at the southern horizon, goes through the overhead – zenith — generally through the North Star — and to the northern horizon.) The meridian divides the rising stars from the setting stars. It marks the highest point a celestial object can reach during that day. For the sun, it is noon. When the sun is east of the meridian, that’s morning; we use the letters “a.m.” (ante meridiem)to designate that the sun is before the meridian. When it is west of the meridian, that’s afternoon and we use the letters “p.m.” (post meridiem) to designate that the sun has past the meridian. For me in that moment of time when the sun is south, it is neither 12 a.m. nor 12 p.m. It is Noon. So next time you meet somebody for lunch, great them with a “Good Noon!” Earlier this year the Internet’s heart fluttered when a NASA expert stated there were 13 “signs” (for example see) in the zodiac. This is not news. The zodiac is the constellations that form the background for the real and apparent movement of the sun, moon and planets. Notice on the chart above that the ecliptic, the plane of our solar system, goes through Ophiuchus, the Snake Handler, which may have been a predecessor to the modern physician. The time that the sun spends in front of the stars of Ophiuchus is longer than the time in Scorpius. This is the constellation that made the Internet’s heart skip a beat. And there are occasions when the moon moves through part of Orion. So there are 14 constellations that form the zodiac. It’s not news, though. Have a happy holiday season. For me, it’s Christmas, so I wish you “A Merry Christmas” and a “Joyous New Year.” For my readers south of the equator, it’s summer. 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Increased processor demands continue to drive advances in central processing units (CPUs), bandwidth and associated memory devices. A CPU typically includes a die, or microchips, which contain multiple processing units, communications hardware, and a local networking or communications bus. The core logic chipsets (cores) are the components that make up the processor die. The cores comprise the central processing logic of a computing system. A system's core logic typically includes a controller for handling memory functions, a cache for storing instructions, the logic for bus interfaces, and the functions of data paths. A single die can contain hundreds of processor cores. In increasing the number of cores, computer performance also increases, as does the need for more memory. For efficiency considerations, the memory-to-processor core ratio must stay relatively constant. That is, as more processors are added, memory must be proportionally added. The need for higher memory to processor-core ratios is further driven by advances in virtualization. Virtualization makes it possible to run multiple operating systems and multiple applications on the same computer at the same time, increasing the utilization and flexibility of hardware. In one respect, virtualization allows the transformation of hardware into software, including the CPU, RAM, hard disk and network controller, to create a fully functional virtual machine that can run its own operating system and applications just like a physical computer. Virtualization is advantageous because it allows for server consolidation and increased processor accessibility. And thus, virtualization is driving the need for even higher memory to processor-core ratios, and higher memory capacity on servers. The increased processing afforded by virtualization requires the addition of memory to maintain the required ratio. For speed considerations, the preferred way to add memory is to attach main memory directly to the CPU. Performance is increased with data being stored directly in main memory, as opposed to slower, remote memory, e.g., memory on a disk. However, attaching memory directly to the CPU typically imposes a limitation on the total amount of available memory. Attached memory may be inadequate for applications requiring larger memory capacities. Caching is commonly used to speed memory processes. A cache memory is smaller, faster and typically more expensive than main memory. When a CPU requests data that resides in main memory, the processing system transmits the requested data to the processor and also may store the data in a cache memory. When the processor issues a subsequent request for the same data, the processing system first checks cache memory. If requested data resides in the cache, the system gets a cache “hit” and delivers the data to the processor from the cache. If the data is not resident in the cache, a cache “miss” occurs, and the system retrieves the data from main memory. Frequently utilized data thus is retrieved more rapidly than less frequently requested data, and overall data access latency, i.e. time between a request for data and delivery of the data, is reduced. In associative mapping, instead of hard-allocating cache lines to particular memory locations, it is possible to design the cache so that any line can store the contents of any memory location. A cache line is the smallest unit of memory than can be transferred between the main memory and the cache. Associativity improves performance by, in part, enabling multiple concurrent accesses to portions of memory. Relatively large amounts of bandwidth are needed to support associativity, however. On some processor memory architectures, for instance, the x86, there is not enough memory bandwidth (the amount of data that can be carried from one point to another in a given time period) to support a cache with associativity. The inability to support cache access with associativity relegates manufacturers to using other, less efficient forms of memory access and lower performance. 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Drosophila reproductive behavior will be studied using genetic tools. Questions on the control, by the various parts of the nervous system, of different features of courtship will be asked with genetic mosaics (following up our earlier studies). What parts of the dorsal brain must be male to allow the early steps of courtship to be performed? Are intermediate steps of courtship controlled by the brain, and if so, by the same parts? The later steps of courtship are controlled by male thoracic tissues: is the thoracic ganglion critically involved in such control? For female behaviors, which tissues must have a female genotype in order that a mosaic be receptive to courtship and copulation, or be able to carry out the post-copulation rejection behaviors? -- Several behavioral mutants affecting courtship have been characterized by behavioral observation and manipulation. Different mutants influence the early, middle, or late stages of courtship sequence. The causes of these reproductive defects will be analyzed, beginning with studies of mosaics: For instance, where in the fly must a small genetic duplication--carrying the normal allele of a gene involved in aberrant male-female and male-male interactions--be present in order that normal behavior occur? Some of the experiments here, on mutants and mosaics, will concern the possible genetic control of particular neural oscillators--those that drive motor output in the courtship lovesong. Also, we are dissecting the control of copulation--its basic duration, the relationship of that duration to sperm transfer, and the details of actions involved in its termination. -- The various mutants may affect the development or the functioning of the nervous system. In this light, we will analyze conditional alleles of certain of the mutants, to ask which stage of the life cycle is influenced by the genetic variants. -- We are asking several questions on triggers and inhibitions of courtship behaviors, influenced by putative pheromones. These experiments are related, not only to studies of normal males and females, but also very strongly to the investigations of behavioral mutants, and to the behavioral dissection of the brain in genetic mosaics.	3.25	3	[ -0.0015869140625, 0.010498046875, 0.0004596710205078125, 0.0238037109375, -0.0233154296875, -0.004913330078125, 0.0098876953125, -0.027099609375, -0.00244140625, -0.01495361328125, 0.004058837890625, 0.0089111328125, -0.0157470703125, -0.002227783203125, -0.0059814453125, 0.00157928466796875, -0.00110626220703125, -0.01397705078125, -0.0034332275390625, 0.005035400390625, 0.0069580078125, 0.0025482177734375, 0.00177764892578125, -0.004608154296875, -0.011962890625, 0.00445556640625, -0.0028839111328125, -0.01123046875, 0.0108642578125, 0.0157470703125, -0.0023956298828125, 0.0133056640625, -0.0220947265625, -0.022216796875, -0.008056640625, -0.0038604736328125, 0.006866455078125, -0.008544921875, -0.013916015625, 0.015625, -0.000946044921875, -0.01611328125, 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Q: Scanf with a specific format I would like to allow the user to only put input in a specific format.The format: a=1,b=-2,c=3 for example. Spaces are allowed inbetween the commas and the characters.I'm using: if (scanf("a=%lf,b=%lf,c=%lf",&a,&b,&c) == 1) but for some reason it doesn't work. How can I fix it? A: You are converting 3 numbers, the return value should be 3 if all conversions are successful. Also note that %lf ignores spaces before the number. If you also want to ignore spaces around the , and before the = or the a, add a space in the format string: double a, b, c; if (scanf(" a =%lf , b =%lf , c =%lf", &a, &b, &c) == 3) { /* conversion was successful, 3 numbers parsed */ ... } Note however that scanf() will not ignore just space characters, it will ignore and whitespace characters, including newlines, tabs, etc.	3.09375	3	[ -0.0096435546875, -0.014404296875, 0.00579833984375, 0.002166748046875, -0.00860595703125, -0.0194091796875, -0.01544189453125, 0.00897216796875, -0.01416015625, 0.010009765625, 0.000888824462890625, -0.0048828125, -0.0255126953125, -0.00141143798828125, 0.00897216796875, 0.00439453125, -0.0205078125, 0.006256103515625, 0.0260009765625, 0.000009417533874511719, 0.0927734375, 0.0107421875, -0.0042724609375, 0.00604248046875, -0.00072479248046875, -0.01214599609375, 0.00775146484375, -0.01239013671875, 0.00836181640625, 0.010498046875, 0.0057373046875, -0.004974365234375, -0.048095703125, 0.00897216796875, 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- 18384239 = 0. Let v = b - -11270494. What is v rounded to the nearest 1000000? 5000000 Let x = -80910709 - -80907455.86056. Let g = x + 3253. Let y = -0.14 - g. Round y to four decimal places. -0.0006 Let u = -0.105 - 0.009. What is u rounded to two decimal places? -0.11 Let y = -0.109956 - -0.11. What is y rounded to 5 dps? 0.00004 Let y = 2132261743607.5999992 + -2132262623126. Let i = 879518 + y. Let d = i + 0.4. Round d to six decimal places. -0.000001 Let j = 222831 + -119831. What is j rounded to the nearest 10000? 100000 Let g = 0.38 - 0.38000006. Round g to seven dps. -0.0000001 Let z = 0 - 0. Let w = 0.3 + z. Let t = -0.82 + w. What is t rounded to 1 decimal place? -0.5 Let d = -0.037 + 0.0369884. Round d to six dps. -0.000012 Let t be 20/(990003/(-330000) - -3). Round t to the nearest 1000000. -2000000 Let s = -8.94 - -9. Let u = 0.0599968 - s. What is u rounded to 6 dps? -0.000003 Let i = 2.6 - 3.16. Let h = i + 0.56000049. What is h rounded to seven decimal places? 0.0000005 Let l be (-4)/(-6) + (-13)/(-3). Let o(s) = -l + 3 + 229s + 0. Let b be o(-2). Round b to the nearest 100. -500 Let f = -7.89999794 + 7.9. Round f to six dps. 0.000002 Let x(f) = -f3 + 2f*2 + 2f - 2. Let t be x(2). Suppose -tv + 3v = -14800. Round v to the nearest 1000. -15000 Let i = 4 - 3.95. Let b = i - 0.04999999. What is b rounded to 7 dps? 0 Let m = 67 + -21. Let x = m + -45.99939. Round x to 4 dps. 0.0006 Suppose 2l + 0q - 5q = 2132846, -4l + 4265702 = -5q. Suppose -16666428 + l = -3k. Round k to the nearest one million. 5000000 Let p = -30 + 19. Let t = 11.0065 + p. What is t rounded to three dps? 0.007 Let d = -387.36 + 267.67. Let n = d + 119. Round n to one dp. -0.7 Let p = -5462.1 - -5462.293272. Let o = p + -0.1634. Let j = o - 0.03. What is j rounded to five dps? -0.00013 Let u = -55.034 + 55. Let d = -6607.97300059 + 6607.939. Let l = d - u. What is l rounded to seven decimal places? -0.0000006 Let v = 16 - 27. Let o = v - -10.99999998. Round o to 7 decimal places. 0 Let o = 5.8 + 1.5. What is o rounded to 0 decimal places? 7 Suppose -2f + 2160000 = f. What is f rounded to the nearest 100000? 700000 Let p be 5 + -3 + 0/2. Suppose -v + 5o + 362893 = -227107, 1770000 = 3v - po. Round v to the nearest 100000. 600000 Let f = -0.39 + 4.19. Let r = f - 3.46. Let b = r - 0.5. Round b to 1 dp. -0.2 Let l = 6.91 + -0.01. Let v = l + 0.1. Let b = v + -14.9. Round b to the nearest integer. -8 Let i = -2.81 - -2.7. Let f = i + 4.61. Let g = 5 - f. Round g to the nearest integer. 1 Let n = 7 - 6. Let b = n - 1.000064. Round b to 5 dps. -0.00006 Suppose 1440 = -5k + f - 2107, -k - 3f - 719 = 0. What is k rounded to the nearest 100? -700 Let f = 3.58 + -3.58507. What is f rounded to 3 decimal places? -0.005 Let b be 35-1(-8)/(-4). What is b rounded to the nearest one hundred? -100 Suppose 202439 = c - 51561. What is c rounded to the nearest 10000? 250000 Let g = 2026 + -2024.817. Let i = -0.033 + g. Round i to 1 dp. 1.2 Let w be 0 - -3 - (-12)/(-3). Let r(m) = -518453m - 471987m + 150441m + 1. Let g be r(w). What is g rounded to the nearest 100000? 800000 Let f(m) = 2 - 3m*2 + 2 - 2m3 + m2 + 5m. Let v be (-10)/3 + (-3)/(-9). Let r be f(v). What is r rounded to the nearest ten? 30 Let r = 62.00082 - 62. What is r rounded to four dps? 0.0008 Let c = 84007713652373762.99999858 + -84007714656568843. Let y = 1004195038 + c. Let k = -42 - y. Round k to seven decimal places. 0.0000014 Let m = 551411 + 4079038. Suppose 5t + 0h = -3h + 24347743, -24347771 = -5t + 4h. Let f = m + t. Round f to the nearest one million. 10000000 Let s = -6 + -6. Let q be s/(-7) + 10/35. Suppose -ql = -3w + 620000, -w = l - 0w + 310000. Round l to the nearest 100000. -300000 Let x = 1.8 + 0.2. Let n = -146.025 - -148. Let p = x - n. What is p rounded to 2 dps? 0.03 Let r = -8 - -8.006. Let z = r + 39.994. Let q = 40.0043 - z. Round q to 3 dps. 0.004 Suppose 0 = f - 6 + 2. Suppose -2u - fg - 155008 = 3u, -u - 3g - 31006 = 0. What is u rounded to the nearest ten thousand? -30000 Let m = -0.49 - -0.48883. Round m to four dps. -0.0012 Let s = -23.894 + 24. Let q = s + -0.10599951. What is q rounded to 7 decimal places? 0.0000005 Let g = -1656177 - -966177. Round g to the nearest 100000. -700000 Let n be (-3)/((6/2)/(-3)). Suppose 0 = 7m - nm + 22400000. What is m rounded to the nearest one million? -6000000 Let s = 540037.15900084 + -540015.159. Let f = s + -22. Round f to seven decimal places. 0.0000008 Let d = 148 + -147.701. Let h = -0.044 + d. Let f = h - 0.025. Round f to one dp. 0.2 Let n = -9 - -3. Let b = -0.3546 - -6.35364. Let s = n + b. Round s to 4 decimal places. -0.001 Let t = -82 - -81.9392. Let p = 0.06 + t. What is p rounded to 3 decimal places? -0.001 Let j = 3.32 + -3.3199358. What is j rounded to five decimal places? 0.00006 Suppose -n - 418 = -0n. Let l = 1918 + n. What is l rounded to the nearest one hundred? 1500 Let x(f) = -2f - 1. Let v be x(-4). Let i(y) = -13264y*2 - 10y + 6. Let g be i(v). Round g to the nearest 100000. -700000 Let n = -0.325 - -0.3. Let d = 0 + n. What is d rounded to 2 dps? -0.03 Let d = -7 - -5.9. Let y = d + 1.1065. Round y to three decimal places. 0.007 Let l = 83 + -79.7. What is l rounded to the nearest integer? 3 Let n = -0.14 + 0.38. Let t = 1.86 + n. Round t to 0 decimal places. 2 Let y be 3 - (-24000 + 1 + 2). Suppose -5w = -w + y. What is w rounded to the nearest ten thousand? -10000 Let f = 1.02 - -60.98. Let a = 4938.54 - 4876. Let s = f - a. What is s rounded to one decimal place? -0.5 Let b = 8181890539 - 8181891304.0734971. Let p = -764.3935 - b. Let j = p - 0.68. Round j to six decimal places. -0.000003 Let u = -16.35 - -0.55. Let w = u + 15.799889. What is w rounded to five decimal places? -0.00011 Let b = -11.23 + -0.45. Let k = b + -0.02. What is k rounded to 0 dps? -12 Let n(k) be the first derivative of -k5/3 - k4/24 - 2k3/3 - 1. Let i(x) be the third derivative of n(x). Let m be i(1). Round m to the nearest ten. -40 Let u = -11.09 + 11. Let h = u - -0.0899912. Round h to six dps. -0.000009 Let a(n) = n2 - 3n - 1. Let g be a(2). Let s be g/(-9) - 2701/3. Round s to the nearest 1000. -1000 Let d = 0.04449 + 0.41145. Let r = d - -0.14436. Let s = -0.6 + r. What is s rounded to 4 decimal places? 0.0003 Let x = 14 - 13.9949. What is x rounded to 3 decimal places? 0.005 Let a = -0.045381 + -2874.804619. Let j = a - -2874.969981. Let h = 0.12 - j. What is h rounded to five decimal places? 0.00002 Suppose -2c = 3c - 3g - 21, 4g - 4 = -4c. Suppose -350 = -a - 2a + 2v, -a = -cv - 105. What is a rounded to the nearest ten? 120 Let v = -2127942 + -10072058. What is v rounded to the nearest 1000000? -12000000 Let t = 30.6 + -16.3. Let x = -14.2999882 + t. What is x rounded to six decimal places? 0.000012 Let x = -0.1 + 1.2. What is x rounded to 0 dps? 1 Let r = 11 - 13. Let p = r + 1.999967. What is p rounded to 5 dps? -0.00003 Let a(i) = -i + 1 - 3 - 2 + i3 - 4i*2 + 6i. Let m be a(3). What is m rounded to the nearest integer? 2 Suppose 116 = -4p + 3q - 234, 4p + 2q + 340 = 0. Let h be p + 2/(-5 - -3). Round h to the nearest 10. -90 Let g(k) = 4 + 5k2 + 0 - 4k*2 + 5k. Let j be g(-4). Let f(z) = z*3 - 1190000. Let h be f(j). Round h to the nearest one hundred thousand. -1200000 Let a = -54.2952 + -0.0048. Let o = a - -49. What is o rounded to the nearest integer? -5 Let p = 7336511 - 7336512.7999993. Let d = 1.8 + p. Round d to seven decimal places. 0.0000007 Let f = 13449710 - 8949710. What is f rounded to the nearest 1000000? 5000000 Suppose 3f + 62935 = -2f. Let n = -24587 - f. Round n to the nearest 10000. -10000 Let m be (-89200003)/(-4) - 15/20. What is m rounded to the nearest one million? 22000000 Suppose 2k + 21664 = k - 2h, -4k = -2h + 86616. Let s = -5969 - k. Let f = s - 108687. Round f to the nearest ten thousand. -90000 Suppose -4v - 2 = -2l, -4l + 0l + 12 = -4v. Suppose 0 = -vi + 5i - 14700. Round i to the nearest 1000. 5000 Suppose 12p = 8p - 16. Let c be p/(-8)8 + -1304. What is c rounded to the nearest one thousand? -1000 Let j = -9 + 10. Let h be 1((1 - -1) + j). Suppose -2300000 = 2o - ho. 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Essays Philosophers who think everyday morality is objective should examine the evidence, argues Joshua Knobe. Imagine two people discussing a question in mathematics. One of them says “7,497 is a prime number,” while the other says, “7,497 is not a prime number.” In a case like this one, we would probably conclude that there can only be a single right answer. We might have a lot of respect for both participants in the conversation, we might agree that they are both very reasonable and conscientious, but all the same, one of them has got to be wrong. The question under discussion here, we might say, is perfectly objective. But now suppose we switch to a different topic. Two people are talking about food. One of them says “Don’t even think about eating caterpillars! They are totally disgusting and not tasty at all,” while the other says “Caterpillars are a special delicacy – one of the tastiest, most delectable foods a person can ever have occasion to eat.” In this second case, we might have a very different reaction. We might think that there isn’t any single right answer. Maybe caterpillars are just tasty for some people but not for others. This latter question, we might think, should be understood as relative. Now that we’ve got at least a basic sense for these two categories, we can turn to a more controversial case. Suppose that the two people are talking about morality. One of them says “That action is deeply morally wrong,” while the other is speaking about the very same action and says “That action is completely fine – not the slightest thing to worry about.” In a case like this, one might wonder what reaction would be most appropriate. Should we say that there is a single right answer and anyone who says the opposite must be mistaken, or should we say that different answers could be right for different people? In other words, should we say that morality is something objective or something relative? This is a tricky question, and it can be difficult to see how one might even begin to address it. Faced with an issue like this one, where exactly should we look for evidence? Though philosophers have pursued numerous approaches here, one of the most important and influential is to begin with certain facts about people’s ordinary moral practices. The idea is that we can start out with facts about people’s usual ways of thinking or talking and use these facts to get some insight into questions about the true nature of morality. Thinkers who take this approach usually start out with the assumption that ordinary thought and talk about morality has an objectivist character. For example, the philosopher Michael Smith claims that we seem to think moral questions have correct answers; that the correct answers are made correct by objective moral facts; that moral facts are wholly determined by circumstances and that, by engaging in moral conversation and argument, we can discover what these objective moral facts determined by the circumstances are. And Frank Jackson writes: I take it that it is part of current folk morality that convergence will or would occur. We have some kind of commitment to the idea that moral disagreements can be resolved by sufficient critical reflection – which is why we bother to engage in moral debate. To that extent, some sort of objectivism is part of current folk morality. Then, once one has in hand this claim about people’s ordinary understanding, the aim is to use it as part of a complex argument for a broader philosophical conclusion. It is here that philosophical work on these issues really shines, with rigorous attention to conceptual distinctions and some truly ingenious arguments, objections and replies. There is just one snag. The trouble is that no real evidence is ever offered for the original assumption that ordinary moral thought and talk has this objective character. Instead, philosophers tend simply to assert that people’s ordinary practice is objectivist and then begin arguing from there. If we really want to go after these issues in a rigorous way, it seems that we should adopt a different approach. The first step is to engage in systematic empirical research to figure out how the ordinary practice actually works. Then, once we have the relevant data in hand, we can begin looking more deeply into the philosophical implications – secure in the knowledge that we are not just engaging in a philosophical fiction but rather looking into the philosophical implications of people’s actual practices. Just in the past few years, experimental philosophers have been gathering a wealth of new data on these issues, and we now have at least the first glimmerings of a real empirical research program here. But a funny thing happened when people started taking these questions into the lab. Again and again, when researchers took up these questions experimentally, they did not end up confirming the traditional view. They did not find that people overwhelmingly favoured objectivism. Instead, the results consistently point to a more complex picture. There seems to be a striking degree of conflict even in the intuitions of ordinary folks, with some people under some circumstances offering objectivist answers, while other people under other circumstances offer more relativist views. And that is not all. The experimental results seem to be giving us an ever deeper understanding of why it is that people are drawn in these different directions, what it is that makes some people move toward objectivism and others toward more relativist views. For a nice example from recent research, consider a study by Adam Feltz and Edward Cokely. They were interested in the relationship between belief in moral relativism and the personality trait openness to experience. Accordingly, they conducted a study in which they measured both openness to experience and belief in moral relativism. To get at people’s degree of openness to experience, they used a standard measure designed by researchers in personality psychology. To get at people’s agreement with moral relativism, they told participants about two characters – John and Fred – who held opposite opinions about whether some given act was morally bad. Participants were then asked whether one of these two characters had to be wrong (the objectivist answer) or whether it could be that neither of them was wrong (the relativist answer). What they found was a quite surprising result. It just wasn’t the case that participants overwhelmingly favoured the objectivist answer. Instead, people’s answers were correlated with their personality traits. The higher a participant was in openness to experience, the more likely that participant was to give a relativist answer. Geoffrey Goodwin and John Darley pursued a similar approach, this time looking at the relationship between people’s belief in moral relativism and their tendency to approach questions by considering a whole variety of possibilities. They proceeded by giving participants mathematical puzzles that could only be solved by looking at multiple different possibilities. Thus, participants who considered all these possibilities would tend to get these problems right, whereas those who failed to consider all the possibilities would tend to get the problems wrong. Now comes the surprising result: those participants who got these problems right were significantly more inclined to offer relativist answers than were those participants who got the problems wrong. Taking a slightly different approach, Shaun Nichols and Tricia Folds-Bennett looked at how people’s moral conceptions develop as they grow older. Research in developmental psychology has shown that as children grow up, they develop different understandings of the physical world, of numbers, of other people’s minds. So what about morality? Do people have a different understanding of morality when they are twenty years old than they do when they are only four years old? What the results revealed was a systematic developmental difference. Young children show a strong preference for objectivism, but as they grow older, they become more inclined to adopt relativist views. In other words, there appears to be a developmental shift toward increasing relativism as children mature. (In an exciting new twist on this approach, James Beebe and David Sackris have shown that this pattern eventually reverses, with middle-aged people showing less inclination toward relativism than college students do.) So there we have it. People are more inclined to be relativists when they score highly in openness to experience, when they have an especially good ability to consider multiple possibilities, when they have matured past childhood (but not when they get to be middle-aged). Looking at these various effects, my collaborators and I thought that it might be possible to offer a single unifying account that explained them all. Specifically, our thought was that people might be drawn to relativism to the extent that they open their minds to alternative perspectives. There could be all sorts of different factors that lead people to open their minds in this way (personality traits, cognitive dispositions, age), but regardless of the instigating factor, researchers seemed always to be finding the same basic effect. The more people have a capacity to truly engage with other perspectives, the more they seem to turn toward moral relativism. To really put this hypothesis to the test, Hagop Sarkissian, Jennifer Wright, John Park, David Tien and I teamed up to run a series of new studies. Our aim was to actually manipulate the degree to which people considered alternative perspectives. That is, we wanted to randomly assign people to different conditions in which they would end up thinking in different ways, so that we could then examine the impact of these different conditions on their intuitions about moral relativism. Participants in one condition got more or less the same sort of question used in earlier studies. They were asked to imagine that someone in the United States commits an act of infanticide. Then they were told to suppose that one person from their own college thought that this act was morally bad, while another thought that it was morally permissible. The question then was whether they would agree or disagree with the following statement: Since your classmate and Sam have different judgments about this case, at least one of them must be wrong. Participants in the other conditions received questions aimed at moving their thinking in a different direction. Those who had been assigned to the “other culture” condition were told to imagine an Amazonian tribe, the Mamilons, which had a very different way of life from our own. They were given a brief description of this tribe’s rituals, values and modes of thought. Then they were told to imagine that one of their classmates thought that the act of infanticide was morally bad, while someone from this Amazonian tribe thought that the act was morally permissible. These participants were then asked whether they agreed or disagreed with the corresponding statement: Since your classmate and the Mamilon have different judgments about this case, at least one of them must be wrong. Finally, participants in the “extraterrestrial” condition were told about a culture that was just about as different from our own as can possibly be conceived. They were asked to imagine a race of extraterrestrial beings, the Pentars, who have no interest in friendship, love or happiness. Instead, the Pentars’ only goal is to maximise the total number of equilateral pentagons in the universe, and they move through space doing everything in their power to achieve this goal. (If a Pentar becomes too old to work, she is immediately killed and transformed into a pentagon herself.) As you might guess, these participants were then told to imagine a Pentar who thinks that the act of infanticide is morally permissible. Then came the usual statement: Since your classmate and the Pentar have different judgments about this case, at least one of them must be wrong. The results of the study showed a systematic difference between conditions. In particular, as we moved toward more distant cultures, we found a steady shift toward more relativist answers – with people in the first condition tending to agree with the statement that at least one of them had to be wrong, people in the second being pretty evenly split between the two answers, and people in the third tending to reject the statement quite decisively. Note that all participants in the study are considering judgments about the very same act. There is just a single person, living in the United States, who is performing an act of infanticide, and participants are being asked to consider different judgments one might make about that very same act. Yet, when participants are asked to consider individuals who come at the issue from wildly different perspectives, they end up concluding that these individuals could have opposite opinions without either of them being in any way wrong. This result seems strongly to suggest that people can be drawn under certain circumstances to a form of moral relativism. But now we face a new question. If we learn that people’s ordinary practice is not an objectivist one – that it actually varies depending on the degree to which people take other perspectives into account – how can we then use this information to address the deeper philosophical issues about the true nature of morality? The answer here is in one way very complex and in another very simple. It is complex in that one can answer such questions only by making use of very sophisticated and subtle philosophical methods. Yet, at the same time, it is simple in that such methods have already been developed and are being continually refined and elaborated within the literature in analytic philosophy. The trick now is just to take these methods and apply them to working out the implications of an ordinary practice that actually exists. Share This Joshua Knobe is an associate professor at Yale University, affiliated both with the Program in Cognitive Science and the Department of Philosophy.

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Social Mining using R 1. 200 tweets are extracted from hashtag “#california” and 200 from hashtag “#newyork”. 2. Then create 2 corpus from the 2 datasets. 3. Preprocess the corpus using {tm} package from R. 4. Compute and display the most frequent terms (words) in each corpus. 5. Create 2 word clouds from the most frequent terms. 6. Compute the sentiment scores, i.e. determine whether words used in the tweets are more positively or negatively charged (emotionally). ![sentimentscores.png](/site_media/media/7d5429b20e891.png) ###Sentiment scores summary:### In general, tweets from both states have positive sentiments. However, it seem like tweets from #california appear to have a more negative connotation than #newyork. ## Facebook API ## 1. Consume 100 most recent Facebook posts by user “joebiden” using getPage() from R’s {RFacebook} package. a. Find the most liked post and it’s popularity. b. Find the most commented post and the number of comments. c. Create a word cloud based on the most popular words used in the most commented post. 2. Consume 100 most recent Facebook posts containing the word “petaluma” using searchPages(). a. Rank the most frequent words and display a barplot of it.

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-ase The suffix -ase is used in biochemistry to form names of enzymes. The most common way to name enzymes is to add this suffix onto the end of the substrate, e.g. an enzyme that breaks down peroxides may be called peroxidase; the enzyme that produces telomeres is called telomerase. Sometimes enzymes are named for the function they perform, rather than substrate, e.g. the enzyme that polymerizes (assembles) DNA into strands is called polymerase; see also reverse transcriptase. The commonly used -ase suffix for naming enzymes was derived from the name diastase. See also Amylase DNA polymerase Category:Chemistry suffixes Category:Biological nomenclature Category:Greek suffixes

3.40625

3

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[/caption] Among one of the first exoplanet systems imaged was HR 8799. In 2008, a team led by Christian Marois at the Herzberg Institute of Astrophysics in Canada, took a picture of the system directly imaging three giant planets. The team revisited the system in 2009 – 2010 with the Keck II telescope and discovered a fourth planet in the system. The new planet, designated HR 8799e, orbits at a distance of 14.5 AU, making it the innermost planet in the system. The other planets all orbit at distances of >25 AU. The images were taken in the near infrared where they are most noticeable because the system is relatively young (<100 Myr) and the planets are still radiating large amounts of heat from their formation. The youth of these planets is part of what makes them an interesting target for astronomers. There exists a controversy in the community of planetary astronomers on the formation method of large planets. One theory states that planets form from a single, monolithic collapse that creates the entire planet’s mass at one time. Another possibility is that the initial collapse forms small cores early on, but then there is substantial growth later, as the planetesimal sweeps up additional material. The discovery of the new planet challenges both theories. Marois states, “none of [the theories] can explain the in situ formation of all four planets.” Thus, a combination of both methods may be in use in the system. Several belts of dust are also known in the system which may help astronomers determine what modes of formation were present. In particular HR 8799e is challenging to an in situ formation because the gravitational perturbations from the parent star should disrupt the formation of large gas planets within 20-40 AU from a single formation. Instead, the new planet would likely have had to been a core collapse with subsequent accretion, or alternatively, moved to its present location via migration. Studying systems such as this may help astronomers better understand the formation of our own solar system. The paper notes that the HR 8799 “does show interesting similarities with the Solar system with all giant planets located past the system’s estimated snow line (~2.7 AU for the Solar system and ~6 AU for HR 8799)”. Additionally, both have debris disks beyond the outer orbits with similar temperatures. Different methods of detecting planetary formation necessarily turn up different types of systems. Radial velocity studies detect massive, close-in planets whereas direct imaging most easily finds more distant planets. These two apparent populations represent different modes of planetary formation and for a full understanding, astronomers will need a continuous sampling that merges the two. Marois notes that we are still far from this goal as “[w]e just do not have enough exoplanets detected by direct imaging (~6 so far)” to make any conclusions besides constraints from the non-detections occurring thus far. To truly merge these two populations, astronomers will likely need to wait until more systems are discovered. Previously, some work has been done to estimate the composition of the atmospheres of the three planets already discovered in the system. These systems have been suggested to have cloudy atmospheres for CH 4 and CO. According to Marois, his team is, “planning more observations on e, but it will be hard. We might have to wait for new instruments, like the Gemini Planet Imager to do it properly.” This new instrument “will put a ‘thumb’ on the star (or what we call a coronagraph) to physically block the star light and allow ‘easy’ detection of nearby faint planets.” While this discovery is a first, it will certainly be one of a long line of exoplanet images. Marois is obviously excited about the ability to directly image planets. I asked him what the single most important thing he wanted readers to get from this research. His response was simple, “That we now have the telescopes and instruments to SEE planets orbiting other stars – that’s really cool! The exoplanet field is still very young and we have so much to learn.”

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Astenois Astenois (Latin pagus Stadunensis) was a pagus, the most basic division of territory in the Roman and Frankish empires. In the Middle Ages, it comprised the parishes of the deaconries of Sainte-Menehould and Possesse. Originally a part of Lotharingia, by the eleventh century its southern part belonged to the Holy Roman Empire and its northern part to the Kingdom of France. The original seat of its counts was at Le Vieil-Dampierre. Traditionally, Astenois, Dormois and Castrice, the three eastern pagi of the archdiocese of Reims were held to belong to the empire. In the eleventh century, as part of a general fragmentation of power in the region, new counties were formed which did not correspond to ancient pagi but were instead named after their main castles. The county of Astenois, which did correspond to an old pagus, became known as the county of Dampierre after its rulers' chief fortress. The counts of Astenois were originally a cadet branch of the counts of Toul. The county was produced through the division of the patrimony of Frederick II. The elder son, Renard III, received Toul, while the younger, Peter, received Astenois. Astenois may originally have been a small fief of the bishops of Toul. It may have passed from the last count of the old line, Renard II, to the first count of the new, Frederick I, through the marriage of the latter to the former's daughter, Gertrude, at the same time as the bishop made Frederick count of Toul (1059). Frederick and Gertrude's son, Frederick II, then divided the patrimony for his sons. __NOTOC__ List of counts and lords Peter Frederick Henry Renard I Renard II Renard III Renard IV Anselm I Anselm II John I John II Notes Sources Further reading Category:Subdivisions of the Holy Roman Empire Category:Medieval France

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Operation IceBridge, NASA's airborne mission to monitor polar ice, is amid its fourth week of flights for the Arctic 2011 campaign. Researchers and crew successfully completed flights from Thule, Greenland, to monitor sea ice and have now moved to Kangerlussuaq, Greenland to focus on flights monitoring the ice sheet. Flying a distance of about 19,000 miles [30,000 kilometers] over the Arctic Ocean, scientists onboard the P-3 collected data during eight sea ice flights based from Thule Air Base. One additional sea ice flight remains to be flown from Kangerlussuaq. Why Fly Sea Ice? Sea ice flights, flown this year from March 16-28, take priority early in the mission's Arctic campaigns. That's because sea ice typically reaches its annual maximum extent in March, and scientists want to collect data before the ice begins to melt and retreat during northern hemisphere's summer. This year, sea ice reached its maximum extent on March 7, reaching 5.7 million square miles and tying for the lowest extent since the start of satellite measurements in 1979. The thickness of Arctic sea ice cover is also declining, on average, throughout the satellite record, according to scientists including Joey Comiso of NASA's Goddard Space Flight Center in Greenbelt, Md. Now, after the Ice, Cloud, and land Elevation Satellite (ICESat) stopped collecting data in 2009, IceBridge continues to collect the data scientists need to observe sea ice thickness. The mission's airborne instrument suite collects lidar and radar data making it possible to monitor both the sea ice freeboard and the snow layer on top of the sea ice. Both measurements are important for quantifying the sea ice thickness and predicting the heat exchange between the Arctic Ocean and the atmosphere. Then, on March 23, the P-3 flew one of the campaign's most challenging flights - an overpass of the U.S. Navy's ICEX camp, an assemblage of tents and shacks drifting on an ice floe north of Fairbanks. On the ground with ICEX was a team of researchers from the Army's Cold Regions Research and Engineering Laboratory and the Naval Research Laboratory, who established a line that would be surveyed from on, below and above the ice. Comparing measurements from each vantage point helps scientists improve the accuracy of sea ice thickness measurements. Sea ice camps are moving targets, drifting along with the wind and ocean currents. The erratic movement makes for a challenging overflight. "The sea ice moves unpredictably, crazy, like a drunken sailor," said John Sonntag of URS Corporation, and the IceBridge instrument team lead. Just before the mission, the camp was floating north at about 66 feet per hour, but by the time the aircraft was nearby it had suddenly veered east at about 660 feet per hour. The flyover required precise coordination with ground teams before and during the flight. The P-3 returned to Thule on March 25 to complete three more science flights before transiting to Kangerlussuaq, the base of operations for the next few weeks. Land Ho! The single remaining sea ice flight planned to fly from Kangerlussuaq will overfly a CRYOVEX site. The sites are designed to calibrate the European Space Agency's ice-observing satellite, CryoSat-2. Overflying the site will help scientist link the ICESat, IceBridge and Cryosat-2 datasets. Meanwhile, IceBridge scientists are working to complete a series of land ice flights. To date, IceBridge has completed four land ice flights over west Greenland. Weather has been favorable in that area, which is typical. Upcoming land ice missions to southeast Greenland will rely on a bit more luck, as low pressure from the Icelandic low commonly produces clouds in the region. Sand Drift ExplainedStavanger, Norway (SPX) Apr 11, 2011 The sand along the south-western coastal rim of Norway has drifted for more than 9000 calendar years. This was triggered by sea-level changes and human activities, new research has found. Researchers in countries such as Denmark, the Netherlands and Poland study sand drift, but most of them are focusing on sand dunes along the coastline, not on the plains further inland. "Sand dunes ... read more The content herein, unless otherwise known to be public domain, are Copyright 1995-2014 - Space Media Network. AFP, UPI and IANS news wire stories are copyright Agence France-Presse, United Press International and Indo-Asia News Service. ESA Portal Reports are copyright European Space Agency. All NASA sourced material is public domain. Additional copyrights may apply in whole or part to other bona fide parties. Advertising does not imply endorsement,agreement or approval of any opinions, statements or information provided by Space Media Network on any Web page published or hosted by Space Media Network. Privacy Statement

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Several plant lectins are known as potent immunomodulatory agents, and they are applied in different experimental models of infection (Afonso-Cardoso et al., [@B1]; Oliveira et al., [@B13]). Recent research has characterized these proteins as potential agonists of Toll-like receptors (TLRs or TLR), a family of mammalian homologs of *Drosophila* Toll protein involved in the detection of microbes and initiating inflammatory responses (O\'Neill et al., [@B14]). In this opinion article, we highlighted some studies of plant lectins as modulators or agonists of TLRs in order to stimulate research interest in this fascinating area and promote knowledge sharing and scientific collaboration. A short view on plant lectins ============================= Lectins are a very large class of carbohydrate-binding proteins of non-immune origin. Through the interaction with sugars, they trigger several important cellular processes. Lectins are universally expressed and have been shown to function in animals, plants, and microorganisms as cell and molecular recognition proteins. However, the carbohydrate-binding domains have been studied most intensively within the plant kingdom (Sharon, [@B16]; Vandenborre et al., [@B20]). The discovery of plant lectins occurred in the 19th century, however, many questions about the biological role of these molecules remain obscure. Lectins may be involved in sugar transport, carbohydrate storage and they are associated as molecular chaperones (Van Damme et al., [@B18a]; Liu and Li, [@B10]). The adhesion and agglutination properties of lectins have been related in the interaction of both symbiotic and pathogenic interaction of some microorganisms and host (Audfray et al., [@B2]). Plant lectins represent a group of proteins with obvious differences in their biochemical/physicochemical properties, molecular structure, carbohydrate-binding specificity and biological activities (Liu et al., [@B9]). Lectins are oligomeric which exhibit a large structural diversity and the molecular size range from 60 to 400 kDa. Each lectin polypeptide contains many molecular domains, one of which is the non-catalytic carbohydrate recognition domain, responsible for their ability to recognize and interact with specific glycoconjugates, without altering their structure. In the past few years, hundreds of plant lectins have been purified and characterized in details with respect to their biochemical properties, carbohydrate-binding specificities, these approaches allowed their classification (Van Dammes et al., [@B19]). Toll-like receptors =================== Plant materials represent an excellent source of immune modulators, which have been appointed as a new approach for combating infections caused by resistant microorganisms (Hancock et al., [@B5]). In this sense, a range of potential compounds have been proposed as agonists or inductors of immune receptors, including TLRs. The TLR family is the best characterized group of innate immune receptors in terms of known ligands, downstream signaling pathways and functional relevance. They comprise a family of receptors homologous to Toll receptor from Drosophila melanogaster. In humans, the TLR family includes 10 transmembrane proteins that play a crucial role in host defense: they recognize molecular characteristics of microorganisms, known as pathogen-associated molecular patterns (PAMPs) highly conserved between different classes of microorganisms. For example, TLR4 and accessory proteins recognize lipopolysaccharide (LPS), while TLR2 recognizes lipoteichoic acid and various lipopeptides (when in complex with either TLR-1 or TLR-6), and TLR5 recognizes flagellin (Hancock et al., [@B5]; O\'Neill et al., [@B14]). In this way, TLR receptors represent important therapeutic targets for developing new drugs able to directly modulate the host response against microbial infection. In fact, some TLR agonists and TLR modulators have been investigated as potential drugs on clinical trials and research programmes (Hennessy et al., [@B6]; Murgueitio et al., [@B12]). Plant lectins and toll-like receptors ===================================== Lectins have been extensively used as valuable tools in the biomedical research. The versatility of these biomolecules is due to their interactions with receptor-linked glycans on cell surfaces, which may trigger cell signaling and physiological responses (Lam and Ng, [@B7a]). Plant lectins are characterized as immunomodulator agent, which result in the production of certain cytokines and reactive species and induce efficient immune responses against tumors or microbial infections. A very comprehensive review of immunomodulatory lectins has recently been published by Souza et al. ([@B17a]). In order to investigate the mechanism of this action, some researchers correlated the activation of immune cells by lectins with the expression of TLR receptors. Sodhi et al. ([@B17]) investigated the expression of different TLRs induced by the famous lectin from Concanavalin A (Con A) using mouse macrophages as a model. Con A enhanced *in vitro* expression of TLRs (2--9) and its action was related with JNK, p38, p42/44, and NF-κ B. The authors also showed the heterodimerization of TLR-2 and TLR-6. Additionally, Con A pre-treated-macrophages were more susceptible to induction of proinflammatory cytokines and nitric oxide by different TLR ligands (ZymosanA, PolyI:C, LPS, CpG DNA). In other study, the Korean mistletoe lectin (KML-C) from *Viscum album coloratum* was shown to be a potent activator of TLR-4. The treatment of mouse peritoneal macrophages with KML-C-induced the upregulation of interleukin-1 receptor-associated kinase-1 (IRAK1) resulting in macrophage activation and TNF-α production, which was not observed when TLR-4 was blocked using a TLR-4-specific neutralizing antibody or TLR-4-deficient macrophages. The expression of TLR-4 was also induced by lectin-like protein from *Anoectochilus formosanus* (IPAF), resulting in the stimulation of TNF-α and IL-1β, CD86, and MHC II and phagocytic activity (Park et al., [@B15]). The capacity to modulate the TLR were explored to combat the experimental infection of *Paracoccidiodes brasiliensis* using native and recombinant KM^+^, a mannose-binding lectin from *Artocarpus integrifolia*. BALB/c mice were infected with *P. brasiliensis* and after 10 days both proteins were separately administered. KM^+^ treatment reduced significantly colony-forming unit and induced higher levels of nitric oxide, INF-α, TNF-α, and IL-12, which was dependent on TLR-2 (Coltri et al., [@B4]). Recently, in a remarkable paper, phytohaemagglutinin (PHA from *Phaseolus vulgaris*) and its isoforms were showed as a specific human TLR-4 agonist during an initial screening. This result encouraged the authors to examine the effects of this and other lectins on external (-2/6, -4, and -5) and internal (-3, -7, -8, and -9) human TLRs. In this research, SBA (Soybean agglutinin from *Glycine max*), PNA (peanut agglutinin from *Arachis hypogaea*), ConA and PHA only stimulated extracellular TLRs (-2/6, -4, or -5): TLR-4 for SBA and PNA; TLR-2/6 for ConA; TLR-2/6, -4 and for PHA-L. In other hand, WGA (wheat germ agglutinin from *Triticum vulgaris*) was the most promiscuous lectin activating all tested receptors, except TLR-3 and -4. The jacalin (from *Artocarpus integrifolia*) was inactive. This variety of TLR agonist pharmacology is related to different sugar ligand specificity of each plant lectins, suggesting that the action is encoded by the carbohydrate recognition motifs on different TLRs (Unitt and Hornigold, [@B18]). TLR agonists have been proposed as adjuvants for vaccines against virus (Behzad et al., [@B3]; Hong et al., [@B7]), bacteria (Hancock et al., [@B5]), parasite (Moon et al., [@B11]) and fungi (LeibundGut-Landmann et al., [@B8]). In conclusion, these observations encourage further studies for the characterization of plant lectins as novel agonists and modulators of TLR receptors. These proteins act by increasing the immune response of the host against microbial infections, thus overcoming their immunosuppressive mechanisms and offers an alternative to combat the increasing drug resistance. These approaches may also provide new insights on TLR biology and aid in the discovery of new targets glycosides useful in therapy. Conflict of interest statement ------------------------------ The Editor and Authors declare that while the authors and reviewer (Rafael E Silva) are affiliated with the same institution there has been no conflict of interest during the review and handling of this manuscript. The authors express their gratitude to the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), to the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), and to the Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco (FACEPE) for research Grants. [^1]: This article was submitted to Antimicrobials, Resistance and Chemotherapy, a section of the journal Frontiers in Microbiology. [^2]: Edited by: James Stach, University of Newcastle, UK [^3]: Reviewed by: Paul D. Brown, University of the West Indies, Jamaica; Rafael De Freitas E. Silva, University of Pernambuco, Brazil

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Prékopa–Leindler inequality In mathematics, the Prékopa–Leindler inequality is an integral inequality closely related to the reverse Young's inequality, the Brunn–Minkowski inequality and a number of other important and classical inequalities in analysis. The result is named after the Hungarian mathematicians András Prékopa and László Leindler. Statement of the inequality Let 0 < λ < 1 and let f, g, h : Rn → [0, +∞) be non-negative real-valued measurable functions defined on n-dimensional Euclidean space Rn. Suppose that these functions satisfy for all x and y in Rn. Then Essential form of the inequality Recall that the essential supremum of a measurable function f : Rn → R is defined by This notation allows the following essential form of the Prékopa–Leindler inequality: let 0 < λ < 1 and let f, g ∈ L1(Rn; [0, +∞)) be non-negative absolutely integrable functions. Let Then s is measurable and The essential supremum form was given in. Its use can change the left side of the inequality. For example, a function g that takes the value 1 at exactly one point will not usually yield a zero left side in the "non-essential sup" form but it will always yield a zero left side in the "essential sup" form. Relationship to the Brunn–Minkowski inequality It can be shown that the usual Prékopa–Leindler inequality implies the Brunn–Minkowski inequality in the following form: if 0 < λ < 1 and A and B are bounded, measurable subsets of Rn such that the Minkowski sum (1 − λ)A + λB is also measurable, then where μ denotes n-dimensional Lebesgue measure. Hence, the Prékopa–Leindler inequality can also be used to prove the Brunn–Minkowski inequality in its more familiar form: if 0 < λ < 1 and A and B are non-empty, bounded, measurable subsets of Rn such that (1 − λ)A + λB is also measurable, then Applications in probability and statistics The Prékopa–Leindler inequality is useful in the theory of log-concave distributions, as it can be used to show that log-concavity is preserved by marginalization and independent summation of log-concave distributed random variables. Suppose that H(x,y) is a log-concave distribution for (x,y) ∈ Rm × Rn, so that by definition we have and let M(y) denote the marginal distribution obtained by integrating over x: Let y1, y2 ∈ Rn and 0 < λ < 1 be given. Then equation () satisfies condition () with h(x) = H(x,(1 − λ)y1 + λy2), f(x) = H(x,y1) and g(x) = H(x,y2), so the Prékopa–Leindler inequality applies. It can be written in terms of M as which is the definition of log-concavity for M. To see how this implies the preservation of log-convexity by independent sums, suppose that X and Y are independent random variables with log-concave distribution. Since the product of two log-concave functions is log-concave, the joint distribution of (X,Y) is also log-concave. Log-concavity is preserved by affine changes of coordinates, so the distribution of (X + Y, X − Y) is log-concave as well. Since the distribution of X+Y is a marginal over the joint distribution of (X + Y, X − Y), we conclude that X + Y has a log-concave distribution. Notes References Category:Geometric inequalities Category:Integral geometry Category:Real analysis Category:Theorems in analysis

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Data circuit-terminating equipment A data circuit-terminating equipment (DCE) is a device that sits between the data terminal equipment (DTE) and a data transmission circuit. It is also called data communication(s) equipment and data carrier equipment. Usually, the DTE device is the terminal (or computer), and the DCE is a modem. In a data station, the DCE performs functions such as signal conversion, coding, and line clocking and may be a part of the DTE or intermediate equipment. Interfacing equipment may be required to couple the data terminal equipment (DTE) into a transmission circuit or channel and from a transmission circuit or channel into the DTE. Usage Although the terms are most commonly used with RS-232, several data communication standards define different types of interfaces between a DCE and a DTE. The DCE is a device that communicates with a DTE device in these standards. Standards that use this nomenclature include: Federal Standard 1037C, MIL-STD-188 RS-232 Certain ITU-T standards in the V series (notably V.24 and V.35) Certain ITU-T standards in the X series (notably X.21 and X.25) A general rule is that DCE devices provide the clock signal (internal clocking) and the DTE device synchronizes on the provided clock (external clocking). D-sub connectors follow another rule for pin assignment. DTE devices usually transmit on pin connector number 2 and receive on pin connector number 3. DCE devices are just the opposite: pin connector number 2 receives and pin connector number 3 transmits the signals. When two devices, that are both DTE or both DCE, must be connected together without a modem or a similar media translator between them, a crossover cable must be used, e.g. a null modem for RS-232 or an Ethernet crossover cable. See also Networking hardware References External links Data Terminating Equipment or Data Circuit-Terminating Equipment speeds, IBM Category:Data transmission Category:Telecommunications equipment

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Various techniques of etching resist-imaged photomasks, silicon wafers or other semiconductor materials have been used in semiconductor fabrication processes. A wet etching technique conducted in an immersion tank is a practical high-throughput, flexible fabrication process. By properly selecting etchant chemicals, etch reactions with the target film are thermodynamically favored over reactions with other films. Desirable etch-rate ratios can usually be obtained. A wet etching method is especially suitable for the blanket etching of polysilicon, oxide, nitride and metal. The method is capable of providing the necessary etch selectivity, a damage-free interface and particle-contamination-free wafers. In more recently developed wet etching technology, automated robotic handling systems and ultra-pure chemicals have been used to further improve particle control and process consistency. A well-controlled wet etching technique is therefore the choice of etching process in VLSI and ULSI fabrication processes. One of the key criteria in carrying out a wet etching process is that the etch products must be soluble in the etchant solution and therefore, no contaminating particles are generated. In an immersion etching process, the volume of the etching tank should be large enough to create enough pressure on the wafer surface in order to dislodge hydrogen gas bubbles evolved during etching reactions; to ensure an accurate balance of the etchant components; to keep the concentration of the etchant relatively constant; and to reduce the number of times the etchant tank must be changed in a production environment. An etchant bath change creates expensive down time, and furthermore, the handling of highly hazardous corrosive materials should be rinimized from a safety standpoint. Wet etching is a frequently used technique for stripping photoresist films from silicon wafers where a complete removal of the resist images without adversely affecting the wafer surface is desired. The resist layer or images should be completely removed without leaving any residues, including contaminant particles that may have been present in the resist. The underlying surface of the photoresist layer should not be adversely affected, for instance, undesirable etching of the metal or oxide surface should be avoided. Liquid etchant strippers should produce reasonable bath yield in order to prevent redeposition of dissolved resist on the wafers. The etchant should completely dissolve the photoresist layer in a chemical reaction, and not just lifting or peeling so as to prevent redeposition. It is also desirable that the etching or stripping time should be reasonably short in order to permit a high wafer throughput. Sulfuric acid (H.sub.2 SO.sub.4) and mixtures of H.sub.2 SO.sub.4 with other oxidizing agents such as hydrogen peroxide (H.sub.2 O.sub.2) are widely used in stripping photoresist or in cleaning a wafer surface after the photoresist has been stripped by other means. For instance, a frequently used mixture is seven parts H.sub.2 SO.sub.4 to three parts of 30% H.sub.2 O.sub.2, or a mixture of 88% sulfuric acid and 12% nitric acid. Wafers to be stripped can be immersed in the mixtures at a temperature between about 100.degree. C. and about 150.degree. C. for 5.about.10 minutes and then subjected to a thorough rinse by deionized water and dried by dry nitrogen. Inorganic chemical resist strippers, such as the sulfuric acid mixtures, are very effective in the residual-free removal of highly postbaked resist. They are more effective than organic strippers and the longer the immersion time, the cleaner and more residue-free wafer surface can be obtained. A typical wet chemical treatment system 10 is shown in FIG. 1. The system has a wet chemical holding tank 12 comprises an inner tank 14 and an outer tank 16. As shown in FIG. 1, the inner tank 14 is usually positioned inside the outer tank 16 and that the sidewall 18 of the inner tank is lower than the sidewall 20 of the outer tank. This allows an operating mode where the inner tank is usually filled first with an etchant chemical through inlets 24 and 26. Inlet 26 to the inner tank 14 also serves as a drain and is connected to drain control valve 28 such that liquid can be drained through outlet 32. Similarly, outlet 34 is connected to the bottom of the outer tank 16 to drain the liquid etchant contained in the outer tank through a drain control valve 36 and the outlet 32. The wet chemical treatment system 10 also includes a recirculating means 40 which has an inlet 42 for receiving a fluid from outlet 34 of the outer tank 16 through passageway 46, and an outlet 44 for feeding to filter means 50. A frequently used recirculating means suitable for the wet chemical treatment system is a mechanical pump that is specially outfitted for transporting corrosive fluids. In such a pump, any components that are in contact with the fluid being pumped is constructed of stainless steel, a corrosion-resistant polymeric material such as Teflon, or a metal coated with a corrosive-resistant polymeric material. The passage tubing 46, the drain control valves 28, 36, and the outlets 26, 34 are similarly constructed of corrosion-resistant materials. The wet chemical treatment system 10 further includes a filter means 50 and a heater means 60. The liquid being pumped by the recirculating means 40 through outlet 44 and passage tubing 52 into inlets 54 and 56 of the filter means 50. The filter means 50 is capable of filtering out particulate contaminants in the wet chemical, especially those of metal particles, such that any contamination of the wafer situated in process tank 14 can be avoided. The filtered wet chemical exits the filter means at outlets 48 and 58 to enter into the heater means 60. In most wet chemical treatment processes, either for cleaning or for etching, the wet chemical can be more efficient in its cleaning or etching function when the temperature of the chemical is raised to above ambient temperature. For instance, for most etching and cleaning processes, a temperature of between about 100.degree. C. and about 150.degree. C. is found to be most suitable. The wet chemical enters the heater through inlet 62 and exits at outlet 66 to return the wet chemical to the inner tank 14 through inlets 24 and 26. The inner tank 14 can be filled with fresh chemicals when needed through a filling means 72 controlled by a fill control valve 74. In the operation of a wet chemical treatment system such as that shown in FIG. 1, the system is normally mounted on a raised floor (or a removable floor) in a semiconductor fabrication facility. A typical mounting method for a wet chemical treatment system is shown in FIGS. 2A and 2B. After the treatment system 10 is positioned on a raised floor 30 with a bottom bracket 38 contacting the floor, the treatment system 10 is fastened to the raised floor 30 by a welded angle 64. The welded angle 64, frequently made of a corrosion-resistant metal, such as stainless steel, is attached to the side frame 68 of the treatment system 10 by bolts 70. Collars 76 are used to secure bolts 70 in their mounting position. The welded angle 64 is further attached to the raised floor 30 by bolts 78 through a horizontal flange 80 of the angle. The thickness of the welded angle or of any other anchoring metal plate should be at least 1 cm. The raised floor is normally fabricated of a grating of aluminum which has a smooth top surface and a corrugated back (not shown). The raised floor 30 may also be fabricated of any other suitable material that has the necessary rigidity and lightweight characteristics for easier removal and installation. The raised floor 30 is positioned on top of an I-beam 82 which is in turn positioned on top of a second I-beam 84. Normally, there is no fastening provided between the raised floor 30 and the top surface 86 of the I-beam 82. The I-beam 82 may be fastened to the second I-beam 84 by any suitable mechanical means such as by bolts, or by welding. The bottom flange 88 of the second I-beam 84 may be fastened to a concrete slab floor 90 by bolts 92. A side view of the welded angle 64 for the wet chemical treatment system 10 is shown in FIG. 2B. In the mounting method shown in FIGS. 2A and 2B, the wet chemical treatment system 10 is only secured to the raised floor 30 that is essentially supported by I-beams that are mounted to a slab floor. The conventional mounting method therefore does not meet the seismic prevention standard that is normally required in fabrication facilities which may be subjected to earthquake damages. The problem can be more serious when the wet chemical treatment system is mounted on a higher floor in a fabrication facility where the effect of an earthquake is more severe. For instance, one of such seismic prevention regulations requires that all equipment foot/frame anchoring mechanism and accessories must be designed to survive a force of 0.35 g.times.2.36, i.e., a force magnified for a 4.sup.th floor installation. It is therefore an object of the present invention to provide a method for mounting a process machine on a removable floor that does not have the drawbacks or shortcomings of the conventional mounting methods. It is another object of the present invention to provide a method for mounting a process machine on a removable floor that meets seismic prevention regulation for the containment of corrosive chemicals in a wet chemical treatment system. It is a further object of the present invention to provide a method for mounting a process machine on a removable floor in a semiconductor fabrication facility such that the process machine can survive earthquakes having a force of 0.35 g.times.2.36. It is another further object of the present invention to provide a method for mounting a semiconductor process machine on a removable floor in a fabrication facility by providing an I-beam equipped with an extended upper flange for supporting the removable floor. It is still another object of the present invention to provide a method for mounting a semiconductor process machine on a removable floor in a fabrication facility by providing an I-beam that is equipped with an extended upper flange for supporting the removable floor and for fastening by mechanical means to the process machine through the removable floor. It is yet another object of the present invention to provide a method for mounting a semiconductor process machine on a removable floor in a fabrication facility by utilizing a modified I-beam for supporting the removable floor and for mounting directly to the process machine. It is still another further object of the present invention to provide an earthquake-proof mounting fixture for mounting a process machine on a removable floor by utilizing an I-beam modified with an extended upper flange for supporting the removable floor and for attaching directly to the process machine through the floor. It is yet another further object of the present invention to provide an earthquake-proof mounting fixture for mounting a process machine on a removable floor by providing an I-beam modified with an extended upper flange for attaching to an L-shaped bracket mounted on the process machine through apertures provided in the removable floor.

3.21875

3

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Introduction {#sec1} ============ When individuals prioritize themselves over their communities, the consequences can damage global economies, scientific institutions and the planet. Philosophers and scientists have debated the origins of human prosociality for centuries ([@ref13]). The study of cooperation has evolved beyond philosophy and consumed the energy of scientists across numerous disciplines, from primatology to economics ([@ref7]; [@ref14]). To better understand the nature of cooperation, we took an interdisciplinary approach that combined neuroeconomics, social and personality psychology, and cognitive neuroscience. We examined the neural systems that guide cooperation in groups, and how these systems are shaped by social norms and individual differences. For many years, *prosocial restraint* models asserted that cooperation stems from deliberate restraint of selfish impulses ([@ref58]; [@ref15]; [@ref31]). More recently, *prosocial intuition* models have argued that cooperation stems from intuition, whereas deliberation always maximizes self-interest ([@ref50]; [@ref48]). Both models carve the mind into two core processes: intuition (i.e. rapid, automatic, reflexive mental processing) and deliberation (i.e. delayed, controlled, reflective processing). They differ on the role these processes play in promoting selfish *vs* collective interest. Despite extensive research on this issue, studies of the mental processes underlying cooperation have yielded mixed evidence for existing theoretical models ([@ref6]; [@ref49]). To help reconcile these issues, we considered an alternative approach to cooperation. *Value-based decision* models argue that the cooperative decisions hinge on preferences that vary between individuals and situations. According to this approach, the neural systems involved in storing, representing and learning value play a role in all decisions, whether they are motor actions, food preferences or cooperative behavior ([@ref9]; [@ref38]; [@ref33]). By specifying the conditions under which cooperation requires effortful deliberation, value-based models explain when (and for whom) interventions to boost cooperation will be most effective. Furthermore, these models can reconcile opposing predictions from prosocial restraint and prosocial intuition models. For instance, consider two car drivers (one prosocial and the other selfish) who witness a collision and decide to pull over and help. Although the driver with prosocial preferences might find the decision to pull over easy, the selfish driver might find the decision hard. Understanding the value each individual places on human welfare may determine which processes produce cooperation. Research on human cooperation often involves social dilemmas, such as the public goods game (PGG). In this economic game, players can make monetary contributions to their group that get multiplied and distributed equally (including to players who keep all their money for themselves). It is in the group's collective interest if all players contribute, but it is in each individual's self-interest to contribute nothing and reap the benefits of other's generosity (i.e. free-riding). Consistent with the prosocial intuition model, faster decisions have been associated with larger group contributions in a PGG, suggesting intuitive cooperation ([@ref50]). However, value-based models posit that longer decisions reflect decision-conflict during choices in which the agent is close to being indifferent between options ([@ref16]). In addition, prosocial individuals (i.e. those who generally help others) are faster to cooperate than free-ride (i.e. prioritize themselves over the group), whereas selfish individuals are faster to free-ride than cooperate ([@ref29]; [@ref32]). Thus, individual differences in prosociality shape which mental computations steer cooperation ([@ref63], [@ref64]). The value-based approach also contends that situational factors shift these mental computations. Increasing the cost of cooperation renders selfish decisions faster and less conflicted ([@ref32]). Therefore, descriptive norms (i.e. perceptions of typical social behavior) may also shape cooperation. Humans have strong needs for belonging and tendencies toward conformity ([@ref1]; [@ref10]; [@ref3]), and norms can increase prosocial behavior ([@ref45]) as well as the intrinsic value of socially preferred stimuli ([@ref66]). Indeed, one's cooperation is related to the mean levels of cooperation of others around ([@ref57]). As a result, it may take more effort to defy group norms---cooperating when others are selfish or free-riding when others are generous. In sum, whether people are faster to cooperate or free-ride depends on their prosocial tendencies and context. We examined whether neural regions involved in decision-making show a similar pattern. While early evidence from neuroimaging studies implicated the ventromedial prefrontal cortex (vmPFC) in affective evaluations ([@ref4]; [@ref56]; [@ref35]), the vmPFC is now widely considered a hub for value-based decision-making. For instance, activity in vmPFC is proportional to the expected value that would be obtained by taking an action ([@ref30]; [@ref38]). In contrast, the dorsolateral prefrontal cortex (dlPFC) is associated with executive function and supports goal pursuit ([@ref8]). Indeed, dlPFC damage impairs executive functions like working memory, reasoning and self-regulation ([@ref67]). Functional connectivity between dlPFC and vmPFC is thought to reflect modulation of value during goal-directed decisions ([@ref26]). Moreover, the connectivity of these regions hinges on individual preferences (e.g. healthy eating among dieters; [@ref26]) and context (e.g. regulating cravings; [@ref28]). In sum, vmPFC activation reflects expected value whereas dlPFC may index overcoming prepotent response tendencies ([@ref2]), decision difficulty ([@ref55]) and goal-directed modulation of vmPFC's expected value signal ([@ref52]). This suggests that individuals' prosociality and the social contexts in which they are embedded should determine the value of cooperation. According to the value-based approach, we should observe greater vmPFC activity during choices that align with one's prosocial tendency since value computations will be higher. Likewise, we should observe dlPFC-vmPFC connectivity during choices that conflict with this tendency, since the dlPFC will need to modulate value signals in the vmPFC to steer decision-making. In this manner, fMRI can provide insight into group-based cooperation. Indeed, past research has found roles for vmPFC and dlPFC in cooperation consistent with a value-based approach ([@ref47]). For instance, people show greater activation in vmPFC when mutually cooperating in a Prisoner's Dilemma ([@ref53], [@ref54]) or when inferring cooperative intentions in others ([@ref11]). However, people show enhanced dlPFC activity when cooperating in a Prisoner's Dilemma with someone who typically defects ([@ref59]) or when trusting out-group members in a Trust Game ([@ref27])---situations that might require modulating prepotent value representations. Moreover, a recent study found that patients with dlPFC damage were less likely to cooperate in a Public Goods Game ([@ref65]), again highlighting that dlPFC can contribute to cooperative choice. To clarify the contributions of these regions in group-based cooperation, we examined here how individual differences and social norms shape vmPFC and dlPFC activity during contributions to public goods. Current research {#sec2} ---------------- We examined two variables that could influence the neural computations underlying cooperation: (1) prosocial tendencies and (2) descriptive norms. We measured brain activity while participants played one-shot PGGs ostensibly with other university students. Prosocial tendencies were measured as the proportion of cooperative PGG decisions made by each participant ([@ref32]). To test that PGG decisions reflected broader individual differences in prosociality, we further measured giving in a dictator game (see Supplemental Section S7). We created prosocial and antisocial social norms by manipulating the feedback from the other university students in the PGG (see [Figure 1](#f1){ref-type="fig"}). To verify these norms, we asked participants to estimate how often students cooperated at each university. These estimates indexed individual differences in norm detection. ![Public goods game with descriptive norm manipulation. (a) At the beginning of each block, participants were instructed, 'You will now encounter students from University \[X/Y\]' with one of the corresponding emblems shown. The base rates were fixed for each university such that 30% of students cooperated in one university (antisocial) whereas 70% of students cooperated in the other (prosocial). Participants alternated between antisocial and prosocial schools (order counterbalanced) for a total of four blocks with 25 trials within each block. **(b)** Each trial consisted of a decision phase (4 s) and a feedback phase (7 s) that was broken down into three stages: (1) each student's contribution to the public pot, (2) the pot multiplying by two and (3) each student's earnings after the pot is evenly divided four ways. Students who gave to the pot were always pictured in blue whereas students who kept their money were displayed in yellow. ITI and ISI durations were jittered in order to dissociate neural activity between decision and outcome phases.](nsaa055f1){#f1} We tested four hypotheses derived from the value-based approach: (VB~H1~) prosocial tendencies will moderate the relative contribution of vmPFC and dlPFC, such that choices aligned with one's tendency (i.e. selfish participants free-riding or prosocial participants cooperating) will elicit greater vmPFC responses whereas (VB~H2~) choices that conflict with one's tendency (e.g. selfish participants cooperating or prosocial participants free-riding) will elicit greater dlPFC-vmPFC connectivity. Social context should moderate activity in these regions, such that (VB~H3~) deviating from group norms (i.e. cooperating with free-riders or free-riding against cooperators) will elicit greater dlPFC-vmPFC connectivity whereas (VB~H4~) complying with group norms (e.g. cooperating with cooperators or free-riding against other free-riders) will elicit greater vmPFC activity. Methods {#sec3} ======= Participants {#sec4} ------------ Our target sample was 45--50 participants. Forty-seven university students (32 female) were recruited (via online posters) from the New York City area and paid \$20 (or two research credit hours). Students (*M* = 20.85, *SD* = 2.60) spanned across 16 north-eastern colleges. All participants were right-handed, healthy, had normal or corrected-to-normal vision, and had no history of psychiatric diagnoses, neurological or metabolic illnesses. The study was approved by the review board of New York University. We report how we determined sample size, all data exclusions, all manipulations and all measures. Five participants were excluded from analyses, leaving a sample of 42 participants. Participants were excluded if they met at least one of the criteria defined prior to data collection: (1) moving at least 3 mm across all scan sessions and (2) reporting suspicion (during debriefing) that their decisions could actually affect the payment of other participants. One participant was excluded due to criterion 1 (\>5 mm motion in each scan session), and four participants were excluded due to criterion 2. Procedure {#sec5} ========= Public goods game {#sec6} ----------------- Participants received instructions on how to play a PGG, including four practice trials and a thorough comprehension quiz. In each round, participants were given \$8.00, which they could either keep for themselves or contribute to benefit the group. Players interacted in groups of four and contributions were doubled and split equally by all group members. On each trial, participants were given 4 s to make a decision and received no payment on trials where no response was recorded. After each choice, participants were shown feedback about the other players' decisions and resulting payouts. An intertrial interval (ITI) signaled the beginning of each round and a fixation cross interstimulus interval (ISI) separated the decision and feedback stages ([Figure 1B](#f1){ref-type="fig"}). ITIs and ISIs were jittered 1--8 s using a Poisson distribution and randomized between participants. Participants were instructed they would never encounter the same player more than once such that each trial resembled a one-shot PGG. Before beginning the game, we informed participants that the other players' decisions were based on previous responses from students attending two universities whose identities we had concealed (labeled University X and University Y; [Figure 1A](#f1){ref-type="fig"}). Participants were further instructed that students from one university were more likely to give their money (prosocial school) whereas students from the other university were more likely to keep their money (antisocial school). We did not specify which university was prosocial and antisocial. Participants alternated between playing with students from the prosocial and antisocial schools across four blocks for a total of 100 trials. The identity of the universities and the order they were encountered were counterbalanced across participants. In reality, we adjusted the base rates such that players from each university gave 70% (prosocial) or 30% (antisocial) of the time. Of the 50 trials playing with the prosocial university, for instance, participants encountered 105 'givers' (out of 150 students) with the following feedback distribution: 0 givers (2 trials), 1 giver (10 trials), 2 givers (20 trials) and 3 givers (18 trials). Earnings across all trials were averaged and paid to participants after the study. Prosocial tendencies were computed for each participant by computing their mean level of cooperation (i.e. the proportion of trials they decided to give). Two survey measures were collected and analyzed for exploratory analyses reported in the supplement: emotional ratings for each PGG outcome (see Supplementary Sec. S1) and group identification with each university ([@ref60]) (see Supplementary Sec. S2). Additional survey measures were collected at the end of the study but are not included in the present analyses[^1^](#fn1){ref-type="fn"}. Dictator game {#sec7} ------------- As an independent measure of prosociality, participants played two dictator games upon exiting the scanner: one with a student from the prosocial school and one with a student from the antisocial school. Participants could allocate anywhere from \$0.00---\$1.00 to each student using a slider bar. The amount given to both groups was averaged into an overall measure of prosociality. At the end of the study, participants were informed that no students were actually going to be paid and they were paid the full \$2.00 they were originally endowed with (regardless of their actual allotment). Explicit estimation {#sec8} ------------------- We next assessed the extent to which students' explicitly learned the social norms. Using a slider bar, participants estimated the percentage of students that cooperated from each school. We took the difference between these scores for each participant to compute a measure of norm detection (i.e. the extent to which students from the prosocial school cooperated more often than the antisocial school). Positive scores indicate students who (correctly) remembered the prosocial school giving more often whereas negative scores indicate students who (incorrectly) remembered the antisocial school giving more often. Behavioral analyses {#sec9} ------------------- Analyses of cooperative behavior were conducted using generalized estimating equations ([@ref39]) (GEE) with an exchangeable correlation structure clustered on each participant[^2^](#fn2){ref-type="fn"}. These procedures account for repeated measures in a regression framework and were implemented using the geepack package ([@ref25]) in R ([@ref12]). We used logistic regression with cooperation operationalized as a binary outcome for each trial (0 = Keep, 1 = Give). Parametric tests were only conducted on measures where we observed insufficient evidence for non-normality (α = 0.05; Shapiro--Wilk test). Otherwise, bootstrap confidence intervals were computed with 10 000 simulations. fMRI data acquisition {#sec10} --------------------- Functional imaging was conducted using a Siemens (Erlangen, Germany) 3.0 Tesla Allegra head-only MRI scanner. Functional images were acquired using a customized multi-echo EPI sequence developed by the NYU Center for Brain Imaging to mitigate the effects of susceptibility artifacts in medial temporal and ventromedial regions (TR = 2000 ms; TE = 15 ms; Flip Angle = 82°; 34 3 mm slices with a 0.45 mm gap for whole-brain coverage, Matrix = 64 × 80; FOV = 192 × 240 mm; Acquisition voxel size = 3 × 3 × 3.45 mm). This sequence has been described in detail in prior work ([@ref24]). Each volume comprised 34 axial slices collected in an interleaved-ascending manner and parallel to the AC-PC line. Data were collected in four sessions, 225 volumes each (7 min and 30 sec). Six scans were acquired at the start of each run and dropped from analysis to allow magnet equilibration. During this time, participants were told which university they would be playing with. Finally, whole-brain high-resolution structural scans (T1-weighted, MPRAGE, 1 × 1 × 1 mm resolution) were acquired from all participants, coregistered with their mean EPI images and averaged together to permit anatomical localization of the functional activations at the group level. fMRI data pre-processing {#sec11} ------------------------ Image analysis was performed using SPM12. Images were corrected for slice-time acquisition and realigned to correct for participant motion, coregistered to structural images, transformed to conform to the default T1 Montreal Neurological Institute (MNI) brain interpolated to 3 × 3 × 3 mm, smoothed using a Gaussian kernel with a full-width-at-half-maximum of 6-mm, corrected for artifacts using the ArtRepair toolbox ([@ref41]) and detrended using the LMGS toolbox ([@ref40]). The blood-oxygenation-level-dependent (BOLD) signal was modeled using a canonical hemodynamic response function. A general linear model (GLM) included (1) onset of give decisions, (2) onset of keep decisions, (3) onset of feedback after give decisions and (4) onset of feedback after keep decisions. Reaction times were entered for decision epoch durations, such that each trial was modeled as having a duration of the participant's reaction time ([@ref23]). Further regressors of no interest included (5) onsets of choice epochs for missed trials (i.e. non-responses), (6) feedback epochs for missed trials, as well as six movement parameters from the realignment stage. A high-pass filter with cutoff period of 128 s was used. To analyze the impact of prosocial tendencies, first-level contrasts for Give \> Keep were generated and entered into a second-level random effects analysis along with each participant's mean cooperation (i.e. proportion of give decisions) as an interaction term. To analyze the impact of descriptive norms, first-level contrasts for Give \> Keep were generated separately for each of the four scanner sessions. Norm-level contrasts were computed for each participant by averaging session contrasts corresponding to each norm and then subtracting the antisocial contrast from the prosocial contrast. These contrasts were then entered into second-level random effects analyses. For a psychophysiological interaction (PPI) analysis of overall choice, vmPFC activity served as a physiological variable, choice type (free-riding *vs* giving) served as a psychological variable, and the interaction of these variables was examined; individual differences in prosociality served as a moderator in a second-level analysis. For a PPI analysis of norm congruence, vmPFC activity served as a physiological variable, choice type (congruent with norm *vs* deviant from norm) served as a psychological variable, and the interaction of these variables was examined; individual differences in norm detection served as a moderator in a second-level analysis. Based on past work, our hypotheses targeted specific regions of interest (ROIs): the vmPFC and the dlPFC. To constrain our analysis to these regions, we used existing ROI masks for vmPFC and dlPFC based on prior work ([@ref65]). These ROIs were constructed with the MarsBar toolbox by combining corresponding structures from the Harvard--Oxford Maximum Probability Atlases ([@ref20]) (see [Supplementary Figure S6](#sup1){ref-type="supplementary-material"}). The vmPFC ROI consisted of the frontal pole, frontal medial cortex, paracingulate gyrus, subcallosal cortex, constrained by rectangular prism X = \[−14, 14\], Y = \[10, 80\], Z = \[−35, 0\]. The dlPFC ROI consisted of the frontal pole, inferior frontal gyrus and middle frontal gyrus, constrained by bilateral rectangular prism X = \[−60, −30 (L); 30, 60 (R)\], Y = \[20, 70\], Z = \[5, 55\]. Small-volume corrections were conducted using these ROI masks. Unless otherwise noted, all analyses were corrected for multiple comparisons using a voxel-wise height threshold of *P* \< 0.001 combined with an appropriate cluster extent to maintain a family-wise error (FWE) rate of *P* \< 0.05, using Gaussian random field theory as implemented in SPM ([@ref21]). ROI effect size estimation {#sec12} -------------------------- Given the difficulty of drawing conclusions from null results, we conducted the following procedure to estimate effect sizes for non-significant contrasts. Using Marsbar, we first extracted each subject's average betas (i.e. predicted amplitude) for each contrast within each ROI mask. We then computed the mean amplitude across 10 000 bootstrapped simulations and report the 95% confidence interval of the resulting distribution of means. Computational model {#sec13} ------------------- We fit a computational model that estimated participants' trial-by-trial expectations about the number of expected givers on each round. This model assumed participants chose to give or keep based on (1) a constant term and (2) the number of expected givers on a given round:$$\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}\begin{equation*} p{G}_t=\frac{1}{1+{e}^{\left(-c+-\beta \times G\right)}} \end{equation*}\end{document}$$where $\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}${pG}_t$\end{document}$ is the probability of giving on trial *t, c* is a constant term, $\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}$\beta$\end{document}$ is a weight on the expected number of givers for that trial and $\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}$G$\end{document}$ is the expected number of givers. Separate estimates of *G* were held for each university. On each trial, *G* was updated for the relevant university using a delta-learning rule:$$\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}\begin{equation*} {G}_t={G}_{t-1}+\alpha \delta \end{equation*}\end{document}$$where $\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}$ \alpha$\end{document}$ is a learning rate parameter and $\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}$\delta$\end{document}$ is a prediction error related to the expected number of givers:$$\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}\begin{equation*} \updelta= Number\ of\ Givers\ - G\end{equation*}\end{document}$$ The number of givers was rescaled to range from −1 to 1, so that the constant term would be interpretable at the mean number of givers. Finally, given that the proportion of givers in each group did not change over time, participants could learn the contingencies relatively early on. We therefore allowed the learning rate to decay over time with a decay parameter *d* between 0 and 1 ([@ref43]):$$\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}\begin{equation*} {\alpha}_t={\alpha}_{t-1}\times d \end{equation*}\end{document}$$ This model was fit using maximum likelihood estimation. We applied parameters derived from the model to each participant's data to compute trial-by-trial estimates for the expected number of givers for each participant (see Supplementary Sec. S5 for more details on the modeling approach and [Supplementary Table S2](#sup1){ref-type="supplementary-material"} for parameter estimates). This time series was entered as a parametric modulator of choice, using the same first-level fMRI GLM described in the primary analysis. This analysis was whole-brain corrected for multiple comparisons. Data availability {#sec14} ----------------- All relevant and deidentified, pre-processed data and materials have been made publicly available at the following OSF link: (<https://osf.io/hfngs/>). Results {#sec15} ======= Behavioral Results {#sec16} ------------------ *Prosocial tendencies.* On average, participants cooperated on 33.57% of the trials (SD = 28.40%). Nonetheless, there were large individual differences between participants, ranging from one participant who always cooperated to seven free-riders who chose to keep on all 100 trials (see [Supplementary Figure S1](#sup1){ref-type="supplementary-material"}). Reaction times did not vary between giving and keeping or between norm condition. However, RTs did depend on individual differences in prosocial tendencies, such that cooperation tended to be faster among prosocial participants (see Supplementary Sec. S3). *Descriptive norms*. To ensure participants encoded the descriptive norm manipulation, we conducted a paired *t*-test to assess whether participants estimated different rates of cooperation between the schools (i.e. norm detection). Participants noticed that students from the prosocial school cooperated more often (*M* = 54.71%, *SD* = 23.37%) than students from the antisocial school (*M* = 32.10%, *SD* = 21.30%), suggesting they learned that group norms differed, *t*(41) = 4.34, *d* = 0.67, *P* \< .001 (see [Supplementary Figure S3](#sup1){ref-type="supplementary-material"}). In turn, descriptive norms impacted cooperation. Participants were more likely to cooperate with students from the prosocial school (*M* = 40.42%, *SD* = 49.08%) than the antisocial school (*M* = 24.08%, *SD* = 42.77%; Odds ratio = 2.15, Wald *χ*^2^(1) = 26.4, *P* \< 0.001; see Supplementary Sec. S3 for reaction time analysis). Moreover, norm compliance (i.e. preferential cooperation with the prosocial *vs* antisocial school) was associated with norm detection (*M* = 22.62%, *SD* = 33.77%; *r*(40) = 0.36, bootstrapped 95% CI: \[0.12, 0.55\]): participants who correctly recalled greater cooperation from the prosocial school were more cooperative towards the prosocial school. Neuroimaging results {#sec17} -------------------- *Overall cooperation*. We first tested whether cooperation and defection overall were associated with neural activation in vmPFC and dlPFC. Such findings could be consistent with models asserting that intuition drives cooperation and deliberation promotes self-interest (prosocial intuition; [@ref50], [@ref51]) or that humans are impulsively selfish and require self-control to cooperate (prosocial restraint; [@ref58]; [@ref31]). We tested the first prosocial restraint hypothesis by examining whether the mean signal within vmPFC (defined through an anatomical region of interest; see Methods) was higher during free-riding as opposed to cooperation (i.e. Give \> Keep). Therefore, seven participants with invariant decisions (i.e. cooperating or free-riding on every trial) were excluded from this analysis, leaving 35 participants. No significant vmPFC activation was observed in this contrast at thresholds with small volume corrections (*p*~voxel~ \< 0.001; *p*~cluster~ \< 0.05). We then examined whether dlPFC activity increased during cooperation *vs* free-riding (i.e. Keep \> Give), but observed no significant difference. We reversed these contrasts to test the two prosocial intuition hypotheses: vmPFC is more active when cooperating (i.e. Keep \> Give) and dlPFC activity increases during free-riding (i.e. Give \> Keep). However, we did not observe significant differences for these contrasts. Bootstrapped 95% confidence intervals of the signal change for cooperative (relative to selfish) choices indicated that mean vmPFC signal may increase up to 0.387% or decrease up to 0.474% whereas mean dlPFC signal may increase up to 0.224% or decrease up to 0.173%. Thus, we found insufficient evidence that these regions were differentially recruited for cooperation or free-riding. These results were not consistent with simplified prosocial restraint or prosocial intuition models of cooperation. Thus, we examined whether activation in these regions depends on cooperative tendencies and social norms. *Prosocial tendencies.* According to the value-based approaches, vmPFC should be more responsive during choices aligned with one's prosocial tendencies: selfish participants should display greater vmPFC responses when free-riding and prosocial participants should display greater vmPFC responses when cooperating (see VB~H1~). This is because vmPFC has been found to represent the difference in value between chosen *vs* unchosen options ([@ref5]; [@ref42]; [@ref24]). As a result, vmPFC activity should be higher for a prosocial participant when giving (i.e. when relative value is higher) than when keeping (i.e. when relative value is lower). For a free-riding participant, the reverse should be true. To test this hypothesis, we entered each participant's mean cooperation into a second-level GLM as an estimate of prosociality, and then tested the interaction between prosociality and decision type (i.e. cooperate *vs* free-ride)[^3^](#fn3){ref-type="fn"}. We observed a cluster of vmPFC for the interaction of Prosociality x Decision, *t*(33) = 4.99, *k* = 53, *p*~cluster~ \< 0.001 ([Figure 2A and B](#f6){ref-type="fig"}; see [Supplementary Table S1](#sup1){ref-type="supplementary-material"})[^4^](#fn4){ref-type="fn"}. Consistent with value-based approach, decisions that aligned with one's prosociality elicited greater vmPFC activity: free-riders had more vmPFC activity when free-riding, whereas cooperators had greater vmPFC activity when cooperating. ![vmPFC activity and dlPFC-vmPFC connectivity is moderated by prosocial tendencies. Average cooperation moderates **(a)** BOLD response in vmPFC and **(c)** right dlPFC activity during Give (*vs* Keep) decisions. Color indicates magnitude of *t* statistic. As an alternate visualization, **(b)** vmPFC cluster betas (*y*-axis) for each participant (*n* = 35) are plotted against the proportion of cooperative trials (*x*-axis). **(d)** Right dlPFC-vmPFC PPI cluster betas (*y*-axis) are plotted against the proportion of cooperative trials (*x*-axis). Robust linear regression fits are displayed with blue lines and surrounding 95% confidence interval band.](nsaa055f2){#f6} We examined whether prosociality moderated dlPFC activity during choices that *conflicted* with prosociality (i.e. selfish participants cooperating or cooperative participants free-riding). For this prosociality × decision interaction, we observed two clusters within right dlPFC (both with equal cluster sizes, *k =* 13*, p*~cluster~ *=* 0.050). More prosocial participants showed greater right dlPFC activity when free-riding whereas participants with selfish tendencies showed greater activity when cooperating (see [Figure 2C](#f6){ref-type="fig"}). Moreover, we obtained the same findings when using a self-report measure of cooperative preferences that was not derived from behavior and was not specific to either norm context. Specifically, after the main task, participants reported how positively and negatively they felt upon giving and keeping; when using relative positive affect during giving *vs* keeping as an alternative measure of individual cooperative preference, we observed the same patterns of activation in vmPFC and dlPFC described above (see Supplemental Figure S5, and Supplementary Sec. S1). Some value-based models also assert that dlPFC and vmPFC become temporally correlated when making more difficult, goal-directed choices (see VB~H2~). To test this prediction, we examined whether functional connectivity between dlPFC-vmPFC was moderated by prosociality. We conducted a psychophysiological interaction (PPI) analysis with the right dlPFC cluster for non-dominant choices ([Figure 2C](#f6){ref-type="fig"}) and the vmPFC cluster for dominant choices as a seed region ([Figure 2A](#f6){ref-type="fig"}). We examined connectivity as a function of cooperative *vs* free-riding decisions, with prosociality serving as an individual difference. Cooperative participants showed greater right dlPFC-vmPFC connectivity when free-riding, whereas selfish participants showed greater connectivity when cooperating, *r*(33) = −0.23, bootstrapped 95% CI: \[−0.56, −0.04\], *t*~R~ = −2.00 ([Figure 2D](#f6){ref-type="fig"})[^5^](#fn5){ref-type="fn"}. In other words, participants showed greater dlPFC-vmPFC connectivity when making choices that ran counter to their prosociality, consistent with the value-based approach. *Social norms.* If norms amplify the value of conformity ([@ref44]), then a value-based approach would predict greater dlPFC-vmPFC connectivity when choosing to deviate from norms (i.e. cooperating in antisocial groups or free-riding in prosocial groups; see VB~H3~). We tested this prediction by conducting another PPI analysis with the dominant choice vmPFC cluster ([Figure 2A](#f6){ref-type="fig"}) as the seed region and the non-dominant choice dlPFC cluster ([Figure 2C](#f6){ref-type="fig"}). We contrasted deviant *vs* compliant decisions (i.e. cooperating with the prosocial group and free-riding with the antisocial group *vs* free-riding with the prosocial group and cooperating with the antisocial group)[^6^](#fn6){ref-type="fn"}. We did not observe any significant connectivity changes across decision type: bootstrapped confidence intervals for deviant (*vs* compliant) choices indicated mean dlPFC connectivity may increase up to 0.172% or decrease up to 0.189%. Our measure of norm detection indicated that not all participants learned the group norms. Since this norm-detection measure was positively associated with behavioral norm compliance, it seemed possible that norms modulated dlPFC-vmPFC connectivity in a manner dependent on how participants perceived the norms. To test this possibility, we conducted an exploratory analysis similar to our individual difference analysis above: we entered individual differences in norm detection as a predictor in the second-level GLM. We observed a positive correlation between norm detection and dlPFC-vmPFC connectivity: participants who correctly perceived the norms elicited greater right dlPFC-vmPFC connectivity when deviating from the group, *r*(33) = 0.50, bootstrapped 95% CI: \[0.22, 0.69\], *t*~R~ = 2.90 ([Figure 3](#f16){ref-type="fig"}). This suggests that vmPFC and dlPFC are more functionally correlated when (a) participants who correctly perceived norms deviated from actual group norms and (b) participants who incorrectly perceived norms complied with group norms, thus deviating from their *perceived* norms. That is, participants who incorrectly perceived norms showed greater vmPFC-dlPFC connectivity when deviating from their *subjectively* perceived norms, much as participants who correctly perceived norms showed greater vmPFC-dlPFC connectivity when deviating from the *objective* norms. ![Norm detection moderates dlPFC-vmPFC connectivity when deviating from the norm. Norm detection moderates right dlPFC-vmPFC connectivity for deviant decisions (e.g. free-riding in the prosocial norm or cooperating in the antisocial norm). Participants (*n* = 34) who perceived relatively more cooperation from the prosocial school *vs* antisocial school (*x*-axis) elicited heightened right dlPFC-vmPFC connectivity when deviating from (*vs* complying with) the group norm (*y*-axis). To mitigate influential points, a robust linear regression fit is displayed with blue line and surrounding 95% confidence interval band.](nsaa055f3){#f16} We examined whether this connectivity predicted norm compliance (i.e. preferential cooperation with the prosocial *vs* antisocial school). We observed an interaction whereby participants with greater right dlPFC-vmPFC connectivity during deviant decisions engaged in greater norm-compliant cooperation, OR = 1.97, 95% CI = \[1.26, 3.10\], Wald *χ*^2^(1) =8.72, *P* = 0.003. This suggests that vmPFC and dlPFC are more functionally correlated when (a) norm-compliant participants deviate from norms and (b) non-compliant participants comply with norms; the latter finding may reflect the fact that non-compliance was correlated with incorrect perceptions of norms, as reported above. We did not observe a relationship between group norms and vmPFC activity (see Supplementary Sec. S6). *Evolving expectations*. Adapting to norms requires people to update and deploy expectations about how others will cooperate. We therefore tested whether neural activity during choice reflected expectations about others' cooperation. We fit participant choices to a computational model of learning and choice, which assumed that people updated an estimate of average cooperation for each group following feedback on each trial. Estimates were updated with a prediction error, or the discrepancy between the actual and expected number of cooperators on each trial. This model allowed us to estimate, in a trial-by-trial manner, the number of givers participants expected while making decisions and analyze whether any neural regions tracked this quantity during choice. Increased expectation of givers during choice was associated with activation near the right temporoparietal junction ([Figure 4](#f17){ref-type="fig"}). Given this region's purported role in theory of mind tasks ([@ref22]), this may reflect increased social cognitive processing during choices where others were expected to cooperate. If so, internalizing social norms may play a key role in future cooperation---a form of social prediction. It also suggests participants dynamically tracked expectations related to norms during decision-making. ![rTPJ activity reflects the expected number of givers during decision-making. The number of givers anticipated during choice on a given trial---as estimated through a computational model of learning and choice---correlates with activation in rTPJ. Color indicates magnitude of *t* statistic.](nsaa055f4){#f17} Discussion {#sec18} ========== Value-based models contend that psychological processes supporting cooperation may hinge on idiosyncratic preferences as well as contextual factors that shift these preferences ([@ref32]; [@ref47]). Consistent with this approach, we find that vmPFC and dlPFC activity during cooperation depends upon individual differences in prosociality and sensitivity to social norms. Specifically, prosocial participants elicited greater vmPFC activity when cooperating as well as heightened right dlPFC activity and dlPFC-vmPFC connectivity when free-riding. Self-serving participants showed the reverse pattern. Thus, neither the vmPFC nor the dlPFC exhibited a consistent role in cooperation, but instead showed greater activation when people acted consistently or inconsistently with their prosocial tendencies, respectively. These findings are consistent with the idea that vmPFC activity reflects a decision value that can be modulated by dlPFC ([@ref52]). In contrast, prominent models rooted in dual-process frameworks argue that cooperation is either reflexive (*prosocial intuition* models) or primarily stems from deliberate self-control (*prosocial restraint* models). Past neuroimaging work rooted in dual-process tradition associated vmPFC with intuitive processing and dlPFC with deliberative processing. Thus, the *prosocial restraint model* implied free-riding would be associated with vmPFC activity and cooperation would be associated with dlPFC activity. In contrast, the *prosocial intuition model* implied cooperation would be associated with greater vmPFC activity and free-riding would be associated with greater dlPFC activity. When adopting this interpretation of vmPFC and dlPFC, our data still suggest that prosocial participants are intuitive cooperators, which conflicts with prosocial restraint models, and that selfish participants are deliberative cooperators, which conflicts with prosocial intuition models. Thus, our findings support a value-based interpretation of vmPFC and dlPFC activity or require a more flexible dual-process model that can account for the moderating roles of prosociality and norms. The current research further indicates that norms shape cooperation. Participants who were most attentive to norms aligned their behavior with norms and showed greater right dlPFC-vmPFC connectivity when deviating from norms, whereas the least attentive participants showed the reverse pattern. Curiously, we found no clear evidence that decisions to conform were more valued than decisions to deviate. This conflicts with work suggesting social norms boost the value of norm compliance ([@ref44]). Instead, our findings suggest that norm compliance can also stem from increased functional connectivity between vmPFC and dlPFC. Our findings raise questions about how people model the dynamic shifts in norms that vary over time and between groups. We fit a computational model of learning to understand how people represent the cooperation expected from each group. Expectation of givers during decision-making was associated with activation in a region near the right temporoparietal junction---a region related to theory of mind ([@ref22]). This finding comports well with recent work ([@ref46]) and suggests that social cognitive systems may interface with the construction of value to guide decisions. The present research highlights two important factors that modulate the neuro-cognitive processes guiding cooperation: prosociality and social norms. Rather than neural activity in vmPFC *always* reflecting either prosocial or selfish behavior, the value of cooperation may be lower among selfish individuals or in selfish environments. The notion that cooperation necessarily stems from reflexive intuitions ignores the possibility that some individuals value the outcomes of others. This idea coheres with evidence that selfish participants more often cooperate by mistake, whereas prosocial participants accidentally prioritize their self-interest ([@ref29]). Thus, intuition may trigger cooperative mistakes from selfish participants but deter prosocial participants from second guessing their cooperation. Conclusion {#sec19} ========== In conclusion, more flexible models are needed to specify when, and for whom, cooperation is intuitive or deliberative. This study highlights the advantage of social neuroscience methods for disambiguating the decision-making processes that guide prosocial behavior. The present findings are largely inconsistent with models that assume one mental process always supports cooperation but are consistent with a value-based approach to understanding cooperation. Although our focus on dlPFC and vmPFC helped constrain our hypotheses, cooperation is complex and draws on a widely distributed network of neural systems implicated in prosocial behavior ([@ref34]; [@ref17]; [@ref18]; [@ref29]; [@ref19]). For instance, other reward-related regions, such as caudate, are involved in prosocial choices ([@ref36]) and may show differential patterns of activation across individuals with strong *vs* weak prosocial preferences. Similarly, as evidence accumulates that moral decisions rely on more dynamic, distributed and multi-faceted neurocognitive processing ([@ref61]), more flexible models of value-based decision-making appear to offer a fruitful account for prosociality. Supplementary Material ====================== ###### Click here for additional data file. We thank E. Owens for assistance with data collection, and members of the New York University Social Perception and Evaluation Laboratory for comments on the manuscript. This work was funded by the New York University Center for Brain Imaging and the US National Science Foundation grant \#1349089 awarded to J.V.B., grant \#1606959 awarded to L.H., and graduate research fellowship awarded to J.W. There are no conflicts of interest to declare. These include the Levenson Self-Report Psychopathy Scale ([@ref37]), Groupiness Scale (Dunham & Van Bavel, unpublished), Social Value Orientation ([@ref62]), and additional demographic information (e.g. political ideology, socioeconomic status, etc.) Unlike traditional OLS regression, GEE parameter estimates are typically evaluated using a Wald *χ*^2^ distribution with 1 degree of freedom. See Krajbich et al., (2015) for or a similar analytic strategy with behavioral data. The *t* statistic reported for this contrast (as well as all subsequent contrasts) refers to the peak voxel within the cluster. We use the *t*~R~ notation to indicate *t* statistics calculated using the robust linear regression procedure with an M estimator available in the MASS package ([@ref01]) for R ([@ref12]). One additional participant was excluded from this analysis because they never cooperated when playing with the antisocial students. This left thirty four valid participants in all fMRI analyses involving descriptive norms.

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Understanding Fusion UNDERSTANDING FUSION Figuring Out Nuclear Fusion.… Contrasted against nuclear fission, the type of nuclear reaction currently in use in our nuclear power plants, nuclear fusion has presented unique challenges that has resisted decades of global efforts and investments into unlocking its secrets. The intense heat and pressure needed to make hydrogen atoms fuse together represents a huge technical problem of nuclear fusion, compared to the simple splitting of heavy atoms (uranium or plutonium) in nuclear fission. Nuclei of lighter atoms collide and fuse together to produce nuclei of heavier atoms and release vast amounts of energy in the process —this is the essence of fusion, and also the energy of this process that powers our Sun. Can we harness this process to meet Earth’s energy demands? Fusion is the process that produces the amazing quantities of energy that pour out of stars, such as our sun. It occurs when light atoms such as hydrogen become so hot that they fuse, into new elements, such as helium, in the process releasing large amounts of energy. The ingredients for this amazing process are abundant on earth, and no greenhouse gases or long-lived nuclear waste are created by fusion. Once harnessed,…Learn more>> euro-fusion.org ccfe.ac.uk- Nuclear fusion is one of the most promising options for generating large amounts of carbon-free energy in the future… To get energy from fusion, gas from a combination of types of hydrogen – deuterium and tritium – is heated to very high temperatures (100 million degrees Celsius). One way to achieve these conditions is a method called ‘magnetic confinement’ – controlling the hot gas (known as a plasma) with strong magnets. The most promising device for this is the ‘tokamak’, a Russian word for a ring-shaped magnetic chamber…Learn more>>ccfe.ac.uk WHY FUSION New, environmentally sustainable forms of electricity will be required to meet the aspirations of a growing world population. By 2050, an expected rise in global population from six billion to nine billion and better living standards could lead to a two to threefold increase in energy consumption. No single technology will fulfil this demand. Each has strengths and weaknesses, and a mix of power sources will be needed to meet the challenges of energy security, sustainable development and environmental protection. Future energy supply options may comprise fossil fuels, nuclear fission, fusion, and renewables. euro-fusion.org- Our current energy landscape is heavily dependent on the fast-depleting fossil fuels, with 80% of the global energy consumption being based on fossil fuels, and changing this dependence is critical for two main reasons. First, to meet the growing energy demand, which is set to increase by 37% by 2040 according to the IEA 2014 Executive Summary, and second, to cut down on the greenhouse gas emissions. Once harnessed, fusion has the potential to be nearly unlimited, safe and CO2-free friendly energy source.euro-fusion.org FUSION PHYSICS…High-school physics teaches us that equally charged particles, instead of colliding, would repel each other. To overcome this repulsion, the nuclei need to collide at high speed, and this is achieved by heating the plasma, which makes all the nuclei whiz around faster. As the plasma gets hotter nuclei start to collide at high speeds, and a small fraction of them stick together, releasing a large amount of energy. euro-fusion.org It seems confusing that energy can be generated by both fusion (the coalescence of two nuclei) and fission (splitting the nucleus), as they appear to be quite opposite processes. The explanation lies in the size of the nuclei… Learn more>>euro-fusion.org FUSION TECHNOLOGYAt the core of the fusion device is a ring-shaped metal vessel. The inner wall of the vessel is lined with removable heat-resistant tiles, and has numerous openings for heating devices and measuring systems. Equally spaced around the device are electromagnets that provide strong magnetic fields to keep the hot plasma away from the reactor walls.…Learn more>>euro-fusion.org JET OPERATIONSLearn more about how tokamaks work by taking a tour through the operation and technology of JET. For anyone looking for even more detail we recommend the book “Focus on” in our download-section.euro-fusion.org JET TECHNOLOGIESJET is a lot more than a doughnut-shaped metal vessel. There is an entire plant comprised of many different systems that work together to create the superheated moments in the torus Myriad systems pump out the air, cool some parts of the experiment, heat others, inject the fuel and control the plasma, and then clean up afterwards, ready to do it all again. euro-fusion.org

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It may be hard to believe in the midst of another contentious election cycle, but the next quarter century in the United States promises to be a period of increasing moderation and stability—at least according to a little-known but compelling theory about how the ratio of available men to available women alters our lives. Ups and Downs of America's Sex Ratio Harvard social psychologist Marcia Guttentag began formulating her theory in 1975, after watching Mozart’s The Magic Flute with her second husband, psychologist Paul Secord, and her two children, Lisa, 16, and Michael, 14. “Nothing is more noble than wife and man, man and wife, and wife and man … [reaching] to the height of Godliness,” sang Papageno and Pamina onstage. Hearing them extoll the virtues of marriage so extravagantly put Guttentag into a kind of “cultural shock,” she later wrote. These were the 1970s, after all, when millions of marriages—including both Guttentag’s and Secord’s first marriages—had collapsed in the chaos of the free love movement spawned during the previous decade. When Guttentag returned home, she and her daughter listened to songs that were popular at the time, all of which had a “love ’em and leave ’em” theme. Why were views on marriage in these two eras—Mozart’s 1790s and America’s 1970s—so very different? Maybe, she conjectured, women were in short supply in Mozart’s day, and perhaps now, in the 1970s, there were just too many women. That became the title of a book Guttentag began writing soon after she had her insight, which she knew was the most important of her career. For the first time in U.S. history, she soon learned, the “availability sex ratio”—the ratio of adult men to adult women who are available to marry—had dropped well below 1.0, to perhaps 0.7 by 1970. This meant that there were now 10 available women for every 7 available men, an excess of millions of women of marrying age. What had caused the sex ratio to drop so dramatically, Guttentag wondered, and what impact did this change have on society? While busy directing two research centers at Harvard University, Guttentag began Too Many Women as a true labor of love. She examined imbalances in the ratio of men to women in various cultures and at various times throughout history and the effects they had on social systems. Among other things, she found that where the sex ratio was high, marriage was stable and women tended to stay home, but where the sex ratio was low (too many women, that is), marriage was unstable and women moved into the workplace. The dramatic differences between Sparta and Athens during the fourth century B.C. drove the point home for Guttentag. Ancient Athens most likely had a sex ratio between 1.43 and 1.74 (based on a historical analysis) because of rampant female infanticide and neglect. With three men for every two women, women were kept uneducated and at home. Sparta, in contrast, was a military state in which males were removed from their families early on to be trained as soldiers. With an extreme shortage of men in Spartan society, girls received educations and even physical training similar to that of boys, and women controlled and inherited property. Fourth century B.C. Spartan women controlled 40 percent of the land and property in Sparta; Athenian women controlled no property at all. But Guttentag’s book was not to be, at least not the way she planned it. On November 4, 1977, just five days short of her 45th birthday, she died from a heart attack while alone in a hotel room in New York City. Her husband, Paul, completed her manuscript, but the book that finally came out in 1983 was academic in nature, not the mainstream “big think” book she intended. With her death, the book deal she had made with a major publisher disappeared, and sex ratio theory stayed mainly in the obscure recesses of various academic specialties. Biologists have looked at the sex ratio in animal populations for generations, typically just by counting the males and females in a pack or herd. The natural sex ratio for the American alligator, for example, is about 0.2, or one male for every five females. That kind of ratio makes sense when males fight a lot and female fertility is low. To study the sex ratio in humans is more challenging, especially if your goal is to determine how the sex ratio affects social systems. Nigel Barber, an evolutionary psychologist based in Birmingham, Alabama, has tested its power more than any other scholar. Among his recent findings: When the sex ratio is low (too many women), women are more slender; when women are in short supply, as was the case in the United States in the 1950s, women are more curvaceous, perhaps because they are trying to look the part of traditional wife and mother. Barber’s studies, which often look at patterns in 40 countries or more, have shown the power of the sex ratio in predicting such things as the rate of nonmarital births, the practice of polygyny, and even the likelihood that men will grow facial hair. The more men there are, he found, the more hair they grow to attract mates. United States Births, 1940-Present In a study of divorces in the U.S. from 1896 to 1992, Barber reports that the divorce rate could be predicted remarkably well from the sex ratio. The success or failure of marriage, in turn, ripples though social systems, affecting prevailing values. When there is an excess of available men—as was true during most of U.S. history because most immigrants are male—marriage is generally revered and values are conservative. When available women outnumber available men, women are set free of the home, and values shift toward liberalism. But a low sex ratio also lowers the living standards of women and causes turmoil in relationships, mainly because men typically have more power in society, which they tend to exercise crudely when there are extra women around. The chaos associated with low sex ratios has been confirmed by several other studies, including a 2010 college-campus investigation by sociologists Jeremy Uecker of Baylor University and Mark Regnerus of the University of Texas at Austin. In a survey of about 1,000 college women, the researchers found that on campuses where women outnumber men, women date less, criticize men more, and are less likely to have a college boyfriend, even though they are also more active sexually. One kind of chaos that seems to flow from a low sex ratio is counterintuitive. In multiple studies that examine this issue both across countries and over time, Barber has shown that a shortage of men is associated with higher rates of rape, violent crime, and assault. When women are in short supply, men compete for resources like good jobs and fancy cars that make them more attractive to potential mates. But when there are too many women, factors such as an absence of fathers from the home and conflict between the sexes act to raise the level of violence. The sex ratio is pushed up or down by many factors, including environmental influences in the womb. A 2010 study conducted in the U.K. found that babies born to two nonsmokers were more likely to be male (birth sex ratio of 1.14), whereas babies born to two smokers were much more likely to be female (birth sex ratio of 0.77). Worldwide, the birth sex ratio is generally above one, about 1.07—nature’s way, perhaps, of compensating for the higher mortality rate of males throughout life. By the time people are in their eighties, however, the sex ratio drops to 0.7 or less. Men are in short supply among the elderly. The sex ratio that is most important in influencing social systems is the one that applies to men and women of mating and child-rearing ages—the availability sex ratio. The fact that women usually prefer marrying men who are slightly older can shift the availability sex ratio up or down almost overnight. This is because the number of people born each year can change dramatically when a war ends or a recession begins. It is this phenomenon, which demographers call the “marriage squeeze,” that led to the enormous excess of available women in the U.S. in the generally liberal 1960s and 1970s. Because of sharp increases in the number of births in the years following World War II and the Korean War, women born two decades later were typically seeking older partners born in years when far fewer babies were born, hence the big drop in the availability sex ratio. So a woman born in 1957, when births were numerous, would, in 1977, be seeking a male born a few years earlier than she—say, in 1954—when far fewer males were born. That’s the “squeeze.” Conversely, birth patterns in the 1970s created an excess of men in the 1990s. In other words, the nationwide shift toward conservatism, and even the election of George W. Bush in 2000, was predictable from sex ratio data. A host of effects produce differences in sex ratios around the world and between racial and ethnic groups. The highest sex ratio in the world right now—4.15—is in Qatar, where thousands of men have immigrated to work on construction and oil projects. The lowest sex ratio—about 0.79—is in Djibouti on the Horn of Africa, where an unemployment rate of 40 to 50 percent has forced men to emigrate. Here in the U.S., African Americans have had a low sex ratio since the era of slavery, in part because they have a low birth sex ratio and in part because many black males are in the military or incarcerated. The absence of men keeps many black women living in poverty, bound to the welfare system. Hispanic Americans, on the other hand, have the highest sex ratio of any ethnic group in the country—over 1.5 for people in their twenties—mainly because far more men immigrate than women. The high sex ratio should make that community politically conservative, yet Hispanics generally support liberal politicians, perhaps because liberal politicians are perceived as more pro-minority and pro-immigrant, overriding the sex ratio influence in this case. In Asian countries, particularly China and India, the ratio of males to females has remained stubbornly and artificially high, causing concern among government officials. Because male offspring are preferred in many Asian cultures, sonograms are now being used to identify female fetuses, which are then aborted in large numbers. The birth sex ratio in China is now an alarming 1.13. The fear in some circles that an excess of men will lead to cultural chaos is actually inconsistent, though, with the views of Secord, Guttentag, and others. Barber’s research suggests, for example, that a high sex ratio generally leads to less violence toward women. But the excess of men in China and India has led to new kinds of abuse—women being abducted from Bangladesh, for example, to serve as brides for single males in India, as well as the trafficking of young women within India. Even the election of George W. Bush in 2000 was predictable from sex ratio data. In relatively stable societies like the U.S., the most powerful factor determining the balance of men and women is that marriage squeeze, and birth patterns over the past 25 years make it possible to estimate the availability sex ratio in the U.S. through the year 2035. The trick here is to determine whether the different numbers of people born each year between 1986 and 2010 are likely to cause marriage squeezes in the future. My computations suggest that we are unlikely in coming years to run into either the liberalism of the ’60s and ’70s (when there were too many women) or the conservatism of the late ’90s (when there were too many men). Instead, we will be trending toward a balance between men and women, and therefore, a prolonged period of moderation in all things political and social: a stable divorce rate, reasonable satisfaction in relationships, and greater gender equality. Absent major natural or human-made disasters that are sex-selective or extreme changes in immigration patterns, the next quarter century should be a time of relative calm. Marcia Guttentag would be pleased. Robert Epstein, senior research psychologist at the American Institute for Behavioral Research and Technology, provided original research for this piece.

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Q: There is an error while using System.out.println when both text and variables I am a beginner in Java so I wrote a program to understand the OOP concepts but it gives me an error when trying to use System.out.println(). Here's the code public static void main(String[] args) { sampleClass ADD = new sampleClass(); Scanner input = new Scanner(System.in); int fNum; int sNum; System.out.println("Enter the first number to Add"); fNum = input.nextInt(); System.out.println("Now enter the second number"); sNum = input.nextInt(); int sum; sum = ADD.add(fNum, sNum); System.out.println("The sum of " fNum " and " sNum " is " sum); } A: Replace this line System.out.println("The sum of " fNum " and " sNum " is " sum); with System.out.println("The sum of " +fNum+ " and " +sNum+ " is " +sum); Please Note: In Java, the operator "+" normally acts as an arithmetic operator unless one of its operands is a String. If necessary it converts the other operand to a String before joining the second operand to the end of the first operand. Examples: If one of the operands is not a String it will be converted: int age = 12; System.out.println("My age is " + age);

3.6875

4

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Geography of Andhra Pradesh Please do not contribute text in a foreign language to English Wikipedia. Your contributions are more than welcome at a Wikipedia in your language. Thank you. Andhra Pradesh lies between 12°41' and 19.07°N latitude and 77° and 84°40'E longitude, and is bordered by Telangana, Chhattisgarh, and Orissa in the north, the Bay of Bengal in the East, Tamil Nadu to the south and Karnataka to the west. Among the other states, which are situated on the country's coastal area, Andhra Pradesh has got a coastline of around 974 km, which gives it the 2nd longest coastline in the nation. Two major rivers, the Godavari and the Krishna run across the state. A small enclave 12 sq mi (30 km²), the Yanam district of Puducherry, lies in the Godavari Delta in the north east of the state. The state includes the eastern part of Deccan plateau as well as a considerable part of the Eastern Ghats. Historically the region comprising the state was known as Andhraapatha, Andhradesa, Andhraavani, and Andhra vishaya. Climate The climate of Andhra Pradesh is generally hot and humid. The summer season in this state generally extends from March to June. During these months the moisture level is quite high. The coastal areas have higher temperatures than the other parts of the state. In summer, the temperature generally ranges between 20 °C and 40 °C. At certain places the temperature is as high as 45 degrees on a summer day. The summer is followed by the monsoon season, which starts during June and continues till September. This is the season for heavy tropical rains in Andhra Pradesh. The major role in determining the climate of the state is played by South-West Monsoons. About one third of the total rainfall in Andhra Pradesh is brought by the North-East Monsoons around the month of October in the state. The winters in Andhra Pradesh are pleasant. This is the time when the state attracts most of its tourists. October to February are the winter months in Andhra Pradesh. Since the state has quite a long coastline, the winters are comparatively mild. The temperature in winter raises from13 °C to 30 °C. Locals and tourists generally find that cotton summer clothes are best suited to coping with the climate of Andhra Pradesh. Divisions Andhra Pradesh can be divided into two regions, namely Coastal Andhra and Rayalaseema. Andhra Pradesh has 13 districts: Anantapur, Chittoor, Kadapa, East Godavari, Guntur, Krishna, Kurnool, Sri Potti Sreeramulu Nellore, Prakasam, Srikakulam, Visakhapatnam, Vizianagaram and West Godavari. Anantapur is the largest district of the state and the 7th largest district in India with an area of 19130 km2. Each district is divided into multiple mandals, and each mandal has many villages. Visakhapatnam is the largest city in the state followed by Vijayawada. Other important cities and towns are Kakinada, Guntur, Rajahmundry, Tirupati, Nellore, Ongole, Kurnool and Eluru. New capital After Telangana was created on 2 June 2014, Andhra Pradesh's erstwhile capital Hyderabad remained in Telangana. Although Hyderabad was set to remain the joint capital of both states for ten years, the new capital is being built at Amaravati only. Notes External links Official website of the Government of Andhra Pradesh Category:Environment of Andhra Pradesh

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Growers shipping their products to distant places encountered the difficulty of having the live plants arrive both alive and without damage. Damage occurs when the plants, and/or the growing medium, becomes dislodged from the containers. This is especially a problem when the shipping container becomes inverted during transportation. When inverted, the weight of the containers crushes the plants so that upon arrival the plants are no longer usable. The present solution is to offer credits and rebates for the plants damaged during shipping. Previous attempts at shipping live products have included the use of plastic overwrap. This approach has the drawback that live plants need exposure to air and sealing them with plastic does not allow respiration necessary for live plants. Another approach has been to use a plastic netting to hold the plants within their containers. Netting has proved insufficient in that plants are still able to fit within holes in the netting and become damaged. There is a need in the art for a system for shipping live plants that protects plants from becoming dislodged from their containers and prevents crushing of the plants if the container becomes inverted during shipping. It is an object of the invention to provide a system for shipping live plants. It is another object of the invention to provide a covering for plants within containers maintaining the plant within the container but allowing for respiration. It is another object of the invention to provide a shipping system preventing crushing of plants when the shipping container is inverted. It is another object of the invention to provide a shipping system for live plants minimizing the loss of plants during shipping. It is still another object of the invention to provide a shipping system which is simple and inexpensive to use. It is yet another object of the invention to provide a shipping system for live plants that safely ships a multitude of plants simultaneously. These and other objects of the invention will become apparent to one of ordinary skill in the art after reviewing the disclosure of the invention.

3.1875

3

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Spatial distribution and temporal variability of arsenic in irrigated rice fields in Bangladesh. 2. Paddy soil. Arsenic-rich groundwater from shallow tube wells is widely used for the irrigation of boro rice in Bangladesh and West Bengal. In the long term this may lead to the accumulation of As in paddy soils and potentially have adverse effects on rice yield and quality. In the companion article in this issue, we have shown that As input into paddy fields with irrigation water is laterally heterogeneous. To assess the potential for As accumulation in soil, we investigated the lateral and vertical distribution of As in rice field soils near Sreenagar (Munshiganj, Bangladesh) and its changes over a 1 year cycle of irrigation and monsoon flooding. At the study site, 18 paddy fields are irrigated with water from a shallow tube well containing 397 +/- 7 microg L(-1) As. The analysis of soil samples collected before irrigation in December 2004 showed that soil As concentrations in paddy fields did not depend on the length of the irrigation channel between well and field inlet. Within individual fields, however, soil As contents decreased with increasing distance to the water inlet, leading to highly variable topsoil As contents (11-35 mg kg(-1), 0-10 cm). Soil As contents after irrigation (May 2005) showed that most As input occurred close to the water inlet and that most As was retained in the top few centimeters of soil. After monsoon flooding (December 2005), topsoil As contents were again close to levels measured before irrigation. Thus, As input during irrigation was at least partly counteracted by As mobilization during monsoon flooding. However, the persisting lateral As distribution suggests net arsenic accumulation over the past 15 years. More pronounced As accumulation may occur in regions with several rice crops per year, less intense monsoon flooding, or different irrigation schemes. The high lateral and vertical heterogeneity of soil As contents must be taken into account in future studies related to As accumulation in paddy soils and potential As transfer into rice.

3.203125

3

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Poverty in America: Social Changes & Global Crises Looking at poverty in the American continent is essential to better understand how the former colonies have evolved into radically different countries. Country by country, analyzing the social and economic paths taken, we can see the effects of discrimination, land ownership, wealth distribution & corruption. If you want to read more on the origins of the huge wealth differences between North America and South America, we recommend the article on the causes of poverty. USEFUL LINKS Poverty in America: The United States ‍Homelessness in the United States Historical overview From the 1950s to the early 1970s, poverty in America (i.e. USA) fell continuously as the economy was booming and the average income was rising. This led to a total elimination of absolute poverty in the country. But at the turn of the 21st century, over 1 in 10 American was poor, 20% of whom where African Americans. The reason for this is that when the 1970s oil crisis hit the USA, poverty climbed up again, only to go down again in the 1990s with the new economic boom. Market liberalization in this mature economy brought more efficiency, while other American developing economies were suffering of its impact. The rise of urban poverty in America The 1970s and 1980s decades are also times when poverty in America became concentrated in urban areas, in particular the old, charming industrial centers. At the same time the population also started to change with the arrival of more and more immigrants from Latin America, reshaping the face of poverty. Urban poverty then tripled in ten years and kept on its expansion onto the 1980s decade. It’s now one of the main features of poverty in America (country and continent). As of 1980, nearly 70% of the urban poor were black, 20% were Latinos, and 10% white. A new face of poverty: immigration and single moms Another thing that changed: the traditional family structure. Like it or not, things have changed and you won’t force an unhappy woman to stay married to her husband anymore. Although, some governments actually tried to by restricting welfare support to families headed by a married couple (talk about government intervention!). Well, that wasn’t the official goal but it was clearly the effect. And millions of single mothers were dropped from welfare support. Demographic changes (immigration) as well as changes in the family structure have had a massive impact on poverty in the US for a couple of decades until things finally stabilized. Now their effect is minor, even though immigrants and single mothers (and their kids) still represent much of the poor. But in a stable way, i.e. the numbers don’t change too much. Yey. Oh no, that’s without counting on the effects of the latest economic crisis! Is poverty in the US completely fake? It’s the old “oh when I was a kid we didn’t have TV nor a microwave oven”. But judging today’s poor on 1970s criteria is just completely absurd because we don’t live like we used to in 1970s. Prices are different, education costs hell of a lot more, living standards and norms are totally different. This means that they simply don’t know the definition of poverty. Speaking of absolute poverty in developed countries is just ridiculous, relative poverty is what matters, in other terms, the capability to fully participate in the life of the nation (having a job, having the Internet and whatnot). Of course the poor today live better than the average in the 1950s, but back then they also used to die of diseases and cancers you can now cure. And today you also need to pay for that somehow. US poverty line and US welfare In comparison to other rich countries, the US ranks usually pretty high in the poverty charts (not a good thing). That’s mostly because of the children and the elderly, who fall disproportionately below the poverty line compared to other groups. Time to get a job, kids. The problem is that in most advanced economies child poverty is usually less than 10% whereas in the US it’s been around 20%. It even rose to 25% recently and the country currently counts 1 in 4 children on food stamps. Good days are gone, baby, gone. Another characteristic of American poverty is the living condition of impoverished single parents – usually moms – who even while they work more than their counterparts in Europe or Australia receive less transfer benefit than in other countries. Since their low paid jobs aren’t enough to maintain the household above the poverty line… well they just fall below that line and make do with poorness. But, this also has some positive impacts on the American economy that lead to an interesting debate. Do you want less inequality or a more competitive economy? Is a middle ground possible? Are there other forms of riches non-measurable in dollars? As far as poverty in America goes, you won’t find all the answers right now (probably not before a decade), but here you can start finding out more on US welfare and the national poverty level. Read more about the national poverty level and US welfare. Meanwhile in Canada ‍A beggar in Canada Income inequalities Looking at the recent history of poverty in Canada you can see that income inequalities have increased from 1980 to 2000, especially during the recession of the early 1990s while a huge surge in immigration brought wages down at a bad time. There were big disparities between, say, retirees who were enjoying a pension greater than ever before and immigrants and industrial workers who generated for the first time concentrated urban poverty in the country. The high level of income of older Canadians hid as well just how poor young workers were by bringing up the average income nationwide. Thus in the 1990s the ones witnessing the most inequalities were the young and the single, who were increasingly unemployed… until the good times came back. Immigrants were facing very low income too, but proportionately speaking they weren’t yet that many and most of the urban poor was still white. Canadian poverty and major transformations The reason that inequalities are important in Canada is that they underline the transformations of the economy and the society. These changes put a lot of pressure on how to best redistribute public resources from health care to housing support in the population. Urban poverty – when over 40% of residents in an area live below the poverty line – indeed appeared in the 1980s in an extensive way throughout the country and has had severe consequences on welfare provision, access to education and the rise of unemployment. Ethnic groups were particularly affected by the phenomenon but since the majority of the urban poor was white nonetheless it hinted at the fact that the problem was structural (rather than discriminative): the job market and the economy. Poverty in America: the Latin side of things ‍Poverty in Latin America Absolute or relative? Poverty in Latin America has always been somewhere in-between: neither completely absolute poverty nor completely relative poverty. What does this mean? On this side of the continent, poverty in America meant not having access to many basic services such as primary health care, education, sometimes also water or electricity, but food for instance hasn’t been that big of an issue. In 1980 only 15% of the population was concerned by malnutrition while almost 50% of Africa and South Asia were. Malnutrition in Latin America However, here again we’re being tricked by the numbers and the averages. Many Latin American countries have had a mostly urban population (over 50%) where food supply isn’t usually a problem. But as of 1980 there were still quite a few that were mostly agrarian societies, where food poverty tends to be higher. Therefore, while the average says that “only” 15% of people lack food in Latin America, this masks the fact that in some countries only 1% of the population suffered from malnutrition while in other neighboring countries it went as high as 50%. Even then, it also depended on the definition of urban area, which is prone to pretty incredible variations across the globe. Whether you include slums and Brazil-style favelas or not makes quite a difference. Slums residents often lack food as well, and on top of that they’re totally cut off from the rest of the population and thus lack access to the most elementary services that provide decent living conditions. Rural poverty in Latin America Yet, in the end absolute poverty in Latin America is mostly rural. In such areas, a radical difference with the development of Northern American countries is that landowners have traditionally made up only 5% of the population (against 70 to 80% in the US and Canada a century ago) and this has dramatically shaped the way Latin American countries have developed with embedded inequalities in their societies. The amount of land that farmers possess nowadays still affects how much food they get and the extent of poverty in America, south of the Rio Grande. It determines whether or not they’ll live below the poverty line. Also, read about poverty in Haiti, and what makes it an exception in Latin America Poverty in Mexico: an American classic? ‍Poverty in America: the main cause of immigration to the US & Canada Very rich and yet very poor Over 40 million people live in poverty in Mexico (that’s about 40% of the population), among whom some 15 million live in extreme poverty, as defined by the World Bank (less than $1.25/day). Strangely, Mexico nonetheless is a pretty rich country – 13th economy in the world – which shows that high GDP doesn’t necessarily mean less poverty, for example if there’s no redistribution whatsoever of the country’s riches. What’s more, having such a high poverty rate puts a huge strain on the economy and hurts the country’s competitiveness (natural correlation between poverty and the economy). This much is one typical aspect of poverty in America where many rich countries have maintained inequalities inherited from the colonial era. As only a few rip the benefits of Mexico’s opportunities and resources (and don’t reinvest their capital in the country), the rest of the economy shrinks, unemployment grows and wages go down. The fault goes directly to Mexico’s rich for making poverty worse. That’s the old story of poverty in America on the Latin side. Poverty and economic crises Now in fact Mexico wasn’t doing too bad until the 1980s. Before that inflation was under control, productivity was rising year by year and GDP per capita used to grow by 3-4% every year. But then in the early 1980s came the economic crisis that hit Mexico and Brazil so hard it devastated their economy. Up to now, all Mexican policies do is still try to fix the consequences of what happened decades ago. At that time the peso suffered a major devaluation, inflation skyrocketed (between 100% to 150%, while you can say that 2-5% is okay/normal), wages plummeted by as much as 40% and public debt rose to over 100% of GDP. Facing that much poverty, millions of Mexicans obviously started migrating to the US and Canada at the same time, as mentioned before. Mexico is a perfect example of how poverty, economic cycles and macro-economy can be intimately connected. Cuba, the black sheep of American poverty A strange case After years of struggle Cuba became in 1959 (officially 1961) an independent socialist country, allegedly fulfilling the dreams of its revolutionary leaders. Now Cuba is a strange spot in the story of poverty in America because in many ways it can’t be considered poor. In many ways it fairs better than many advanced economies in terms of equality and quality of services it offers its population. Yet, both the population and the state are becoming penniless which puts the whole system at risk. As the country is running broke and was hit hard by the 2008 economic crisis, there is a dire need for profound reforms and changes in the economy. Historical review of Cuba and its poverty levels For the 30 years following its independence Cuba’s GDP rose by 4% per year, even though 20 to 30% of its GDP was in fact made of aid coming from the USSR. But in the end Cuba boasts today an HDI (Human Development Index) of 0.8, one of the highest in the developing world. The reason for such high HDI is that the index gives great importance to access to education and health care, and Cuba happens to offer universal access to both. So, a healthy and very well educated workforce… but there are no jobs to up to the local level of education. Sounds like the perfect definition of waste of talent and “human capital”. The challenge for Cuba, as you’ll have understood, is to adapt to this post-soviet world of ours and handle the transition and reforms that have recently caused waves of inequalities. But Cuba also holds a few keys regarding how poverty in America can best cope with issues related to globalization and liberalization, which have brought massive inequalities to the whole continent. These content links are provided by Content.ad. Both Content.ad and the web site upon which the links are displayed may receive compensation when readers click on these links. Some of the content you are redirected to may be sponsored content. View our privacy policy here. Family-Friendly Content Website owners select the type of content that appears in our units. However, if you would like to ensure that Content.ad always displays family-friendly content on this device, regardless of what site you are on, check the option below. Learn More Only recommend family-friendly content To learn how you can use Content.ad to drive visitors to your content or add this service to your site, please contact us at info@content.ad. 10Google +0 NEW COMMENTS Hey there ❤ ! Looks like you’re enjoying the discussion. Leave a comment below or sign up to our newsletter to receive our latest articles.

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It is particularly preferred to employ Staphylococcal genes and gene products as targets for the development of antibiotics. The Staphylococci make up a medically important genera of microbes. They are known to produce two types of disease, invasive and toxigenic. Invasive infections are characterized generally by abscess formation effecting both skin surfaces and deep tissues. S. aureus is the second leading cause of bacteremia in cancer patients. Osteomyelitis, septic arthritis, septic thrombophlebitis and acute bacterial endocarditis are also relatively common. There are at least three clinical conditions resulting from the toxigenic properties of Staphylococci. The manifestation of these diseases result from the actions of exotoxins as opposed to tissue invasion and bacteremia. These conditions include: Staphylococcal food poisoning, scalded skin syndrome and toxic shock syndrome. SpoIIIE is a membrane bound protein involved in chromosome partitioning during sporulation and vegetative replication in a wide variety of bacteria. The SpoIIIE gene was initially characterised in Bacillus subtilis (Butler P. D. and Mandelstam J. (1987) Journal of General Microbiology 133:2359-2370). SpoIIIE protein has an ATP binding site and is membrane-bound, and appears to form a pore in the nascent spore septum, through which the prespore chromosome is driven in a conjugation-like mechanism (Wu L. J., Lewis P. J., Allmansberger R., Hauser P. M. and Errington J. (1995) Genes and Development 9:1316-1326). spoIIIE mutants cannot sporulate as they are unable to partition the prespore chromosome into the polar prespore compartment. Instead a specific chromosomal segment comprising approximately 30% of the chromosome enters the prespore, while the rest remains in the mother cell, trapped by the septum (Wu L. J. and Errington J. (1994) Science 264:572-575). In wild-type cells SpoIIIE is membrane-bound, and appears to form a pore in the nascent spore septum, through which the prespore chromosome is driven in a conjugation-like mechanism (Wu L. J., Lewis P. J., Allmansberger R., Hauser P. M. and Errington J. (1995) Genes and Development 9:1316-1326). It has been shown that SpoIIIE is also required for correct partitioning of the B.subtilis chromosome during vegetative cell division. spoIIIE- Mutants in which replication has been artificially delayed are unable to separate the replicated chromosomes before septum formation, resulting in a trapped nucleoid similar to that formed at the start of sporulation (Sharpe M. E. and Errington J. (1995) Proceedings of the Natural Academy of Sciences USA 92:8630-8634). SpoIIIE has been shown to be essential in Escherichia coli (Begg K. J., Dewar, S. J. and Donachie W. D. (1995) Journal of Bacteriology 177:6211-6222). Highly conserved SpoIIIE homologues are found in diverse members of the eubacteria such as Campylobacter jejuni (Miller, S., Pesci E. C. and Pickett C. L. (1994) Gene 146:31-38), Coxiella burnetii (Oswald W. and Thiele D. (1993) Journal of Veterinary Medecine B40:366-370), Eshcerichia coli (Begg 1995 above) and Haemophilus influenzae (Fleischmann, R. D., Adams, M. D., White, O., Clayton, R. A., Kirkness, E. F., Kerlavage, A. R., Bult, C. J., Tomb, J.-F., Dougherty, B. A., Merrick, J. M., McKenney, K., Sutton, G., FitzHugh, W., Fields, C. A., Gocayne, J. D., Scott, J. D., Shirley, R., Liu, L.-I., Glodek, A., Kelley, J. M., Weidman, J. F., Phillips, C. A., Spriggs, T., Hedblom, E., Cotton, M. D., Utterback, T. R., Hanna, M. C., Nguyen, D. T., Saudek, D. M., Brandon, R. C., Fine, L. D., Fritchman, J. L., Fuhrmann, J. L., Geoghagen, N. S. M., Gnehm, C. L., McDonald, L. A., Small, K. V., Fraser, C. M., Smith, H. O. and Venter, J. C. (1995) Science 269:496-512). All of these proteins are 36-55% identical at the amino acid level overall. Their N-terminal 200 amino acids are hydrophobic and not conserved, so if the C-terminal 500 or so amino acids are considered alone the level of conservation rises to 42-67% identical amino acids. This high level of identity among diverse eubacteria strongly suggests commonality of function. Inhibitors of SpoIIIE proteins would prevent the bacterium from establishing and maintaining infection of the host by preventing it from correctly partitioning the chromosome in the manner described above and thus arresting cell division and growth, rendering the bacterium susceptible to host defences and leading ultimately to cell death and thereby have utility in anti-bacterial therapy. Clearly, there is a need for factors that may be used to screen compounds for antibiotic activity and which factors may also be used to determine their roles in pathogenesis of infection, dysfunction and disease. There is also a a need for identification and characterization of such factors and their antagonists and agonists which can play a role in preventing, ameliorating or correcting infections, dysfunctions or diseases. The polypeptides of the invention have amino acid sequence homology to a known B. subtilis spoIIIE protein.

3.140625

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Since the first US case of coronavirus disease 2019 (COVID-19) infection as identified in Washington State on January 20, 2020, more than 235 000 cases have been identified across the US in just over 2 months. Given the challenges in expanding testing capacity and the restrictive case definition of persons under investigation, the true number of cases is likely much higher. By March 17, the outbreak had expanded from several isolated clusters in Washington, New York, and California to all 50 states and the District of Columbia. As of April 2, there have been more than 5000 COVID-19–associated deaths in the US. With a global total now of more than 1 million cases, the US is now the country with the largest number of reported cases, comprising about one-fifth of all reported infections. With community transmission firmly established, the US epidemic enters the exponential growth phase in which the number of new cases is proportional to the existing number of cases. This phase continues until either enough susceptible individuals become immune as a result of infection, stringent public health measures are followed, or both. Case Fatality A yet unanswered question that adds to uncertainty around the outbreak involves the case-fatality rate (CFR), defined as the percentage of deaths among all cases. Presently, global mortality is reported at 4.7% but this varies widely by location from a high of 10.8% in Italy to a low of 0.7% in Germany. Several factors influence the CFR including a reliable estimate of the total number of cases. Among the first 140 904 cases in the US, 1.7% died; however, given the uncertainty in the denominator, this is not a reliable CFR estimate. For example, the crude CFR in Wuhan, China, was reported to be 5.8% on February 1, whereas more methodologically robust estimates using novel methods to estimate the actual number of cases reported the CFR as 1.4%.1 In the coming weeks, surge capacity at US hospitals will influence the CFR. However, to have reliable estimates, better approximations of the overall population (denominator) are essential, and methods such as serosurveys using statistical sampling generalizable to the populations of interest will inform these estimates. New Clinical and Epidemiological Insights Is PCR Always Positive? What Is the Meaning of a Negative PCR? Several types of tests are being used to identify severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).2 These can be classified into 2 general categories: molecular diagnosis/polymerase chain reaction (PCR)–based testing and serological testing. In clinical settings, PCR-based testing remains the primary method of identifying SARS-CoV-2. Given the lack of a reference standard for diagnosing COVID-19, the sensitivity and specificity of diagnostic testing are unknown. In addition, inadequate sample collection may reduce test sensitivity. In a study of 5 patients, individuals with chest computed tomography findings compatible with COVID-19, and a negative reverse transcriptase (RT)–PCR result for SARS-CoV-2, tested positive on subsequent testing, suggesting that certain patients (eg, with compatible radiological findings) might require repeat testing with specimens collected from multiple sites in the respiratory tract.3 It is likely that lower respiratory samples (eg, minibronchial alveolar lavage) are more sensitive than a nasopharyngeal swab. Thus, it is important to emphasize that, depending on the clinical presentation, a negative RT-PCR result does not exclude COVID-19. Multiple serological tests are in various stages of development. With wider availability of serological testing, it will be possible to determine whether patients have a false-negative PCR result. Can Patients Become Reinfected? Reports from China and Japan have indicated that some patients with COVID-19 who were discharged from the hospital after a negative RT-PCR result were readmitted and subsequently tested positive on RT-PCR. It is unclear from the available information if these were true reinfections or the tests were falsely negative at the time of initial discharge. However, while other coronaviruses demonstrate evidence of reinfection, this usually does not happen for many months or years. Therefore, it is unlikely that these were true cases of reinfection. Some reassuring evidence comes from a challenge study among rhesus macaques.4 After initial challenge and clearance of SARS-CoV-2, the animals were rechallenged with the virus but were not infected. While the evidence on reinfection is evolving, current data and experience from previous viruses without substantial seasonal mutation do not support this hypothesis. How Long Does Immunity Last? Presently, there is no validated immune correlate of protection for SARS-CoV-2, ie, antibody level or another immunological marker associated with protection from infection or disease. However, in a study that included 82 confirmed and 58 probable cases of COVID-19 from China, the median duration of IgM detection was 5 days (interquartile range, 3-6), while IgG was detected at a median of 14 days (interquartile range, 10-18) after symptom onset.5 Because the outbreak is only a few months old, there are no data on long-term immune response. Data from SARS-CoV-1 indicate that titers of IgG and neutralizing antibodies peaked at 4 months after infection, with a subsequent decline through at least 3 years after infection. Should Everyone Wear a Mask in Public? Current guidelines from the Centers for Disease Control and Prevention (CDC) do not recommend routine use of medical masks among healthy individuals and suggest limiting mask use to health care workers and those caring for patients with COVID-19. However, this guidance is likely to be modified. Regardless, any change in policy should prioritize the availability of masks for health care workers. Priority should also be given to others with risk of exposure such as first responders and incarcerated individuals. Due to the current scarcity of masks, many in the community have begun sewing masks for themselves and for health care workers. A fitted N95 respirator is the preferred type of medical mask for health care workers; however, supplies in the US are very limited. Medical masks are also recommended for symptomatic individuals to prevent them from transmitting the virus. The rationale supporting the recommendations comes from studies finding limited to no efficacy of masks in protecting healthy individuals from influenza infection and also for the need to preserve supplies. However, evidence from influenza studies might not be relevant for COVID-19. For example, in a systematic review, masks, particularly combined with other measures such as handwashing, were found to be effective in preventing SARS-CoV-1 infection.6 Moreover, with the increasing evidence of presymptomatic transmission of SARS-CoV-2, there might be value in the use of masks among individuals at risk of transmission.7 How Does SARS-CoV-2 Spread? Current evidence suggests that SARS-CoV-2 is primarily transmitted through droplets (particles 5-10 μm in size). Person-to-person transmission occurs when an individual with the infection emits droplets containing virus particles while coughing, sneezing, and talking. These droplets land on the respiratory mucosa or conjunctiva of another person, usually within a distance of 6 ft (1.8 m) but perhaps farther.8 The droplets can also settle on stationary or movable objects and can be transferred to another person when they come in contact with these fomites. Survival of the virus on innate surfaces has been an important topic of discussion. While there are few data, the available evidence suggests that the virus can remain infectious on inanimate surfaces at room temperature for up to 9 days. This time is shorter at temperatures greater than 30° C. The good news is that cleaning and disinfection are effective in decreasing contamination of surfaces, emphasizing the importance of high-touch areas.9 Transmission through aerosols, particles smaller than 5 μm, can also occur under specific circumstances such as endotracheal intubation, bronchoscopy, suctioning, turning the patient to the prone position, or disconnecting the patient from the ventilator. Cardiopulmonary resuscitation is another important aerosol-generating procedure. In a recent study of environmental sampling of rooms of patients with COVID-19, many commonly used items as well as air samples had evidence of viral contamination.10 In the context of the heterogeneity in evidence and possibility of aerosolization of the virus during certain medical procedures, public health agencies (including the CDC) recommend airborne precautions in situations involving patients with COVID-19. When Can Social Distancing Measures Be Lifted? With the exponential increase in US COVID-19 cases and deaths, several jurisdictions have implemented social-distancing measures. Modeling and empirical studies suggest that social-distancing measures can help reduce the overall number of infections and help spread out cases over a longer period of time, thus allowing health systems to better manage the surge of additional patients. However, long-term social distancing can have detrimental effects on physical and mental health outcomes as well as the economy. A few changes may allow for easing restrictions: First, an aggressive program of testing to identify asymptomatic and mild cases combined with proactive contact tracing and early isolation as well as quarantine of contacts. Second, there must be a focus on reducing home-based transmission. In Wuhan, particularly after the initial phase, most transmissions occurred within households. While the CDC has published guidelines for preventing household transmission, it did not place enough emphasis on the importance of having the infected person always wear a mask. Third, even a treatment that only shortens an intensive care unit stay by 20% to 30% can have a substantial benefit on health system capacity. When Will a Vaccine Be Available? The ultimate strategy for controlling this pandemic will depend on a safe and efficacious vaccine against SARS-CoV-2. However, only 3 vaccine candidates are currently in phase 1 human trials: a messenger RNA vaccine and 2 adenovirus vector-based vaccines. The estimated timeline for availability of an initial vaccine is between early and mid-2021. Conclusions As the COVID-19 outbreak expands in the US, overall understanding of this disease has increased, with more information available now than even a few weeks ago. However, more evidence is needed, particularly for public health and clinical interventions to successfully prevent and treat infections. Even during a pandemic, obtaining rigorous, reliable data is not a distraction, rather it is essential for accurately measuring the extent and severity of COVID-19 and assessing the effectiveness of the response. Back to top Article Information Corresponding Author: Carlos del Rio, MD, Emory University School of Medicine, 49 Jesse Hill Jr Dr SE, FOB Room 201, Atlanta, GA 30303 (cdelrio@emory.edu). Published Online: April 6, 2020. doi:10.1001/jama.2020.5788 Conflict of Interest Disclosures: Dr del Rio reported receiving grants from the National Institutes of Health/National Institute of Allergy and Infectious Diseases. No other disclosures were reported.

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Materials scientists have created a substance called 'new diamond.' It has the hardness of diamonds, without one of their very significant weaknesses. Unfortunately, the 'new diamonds' don't have their advantageous sparkle either. Learn about the strength behind diamond's 'ugly stepsisters.' Diamond is one of the hardest substances in the world. It's able to withstand scratching and pressure and incredible shocks, or at least that's what we've been told. Although diamonds have been held up as an amalgamation of strength and beauty, their beauty is actually their weakness. They're crystals. A crystal is formed when atoms, in this case carbon atoms, are locked into a repeating structure. The structure is patterned, but it is not symmetrical in every direction. Hit the structure one way and it's hard as, well, a diamond. Hit it another way and it has only a small fraction of the hardness. Enter 'new diamond.' This material is created from a material first made in the 1950s called 'glassy carbon.' Glassy carbon is a hard, difficult-to-melt, glass-like substance that's often used because of its durability. Compress that to 400,000 times atmospheric pressure and you create the dark, slightly shiny material of new diamond. It can take 1.3 million times atmospheric pressure, a feat only matched by diamonds. Unlike diamonds, new diamond is not a crystalline structure but an amorphous material - aka a blob. Since its molecules are oriented any which way, they can be hit any which way and stand up to the same pressure. And what will scientists do with this new wonder material? The first idea is to make new diamond into an anvil, on which they can make even denser and harder materials.

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Lake Baikal, in eastern Siberia, is no ordinary lake. Here are some interesting facts about it: » Lake Baikal is the deepest lake in the world with a maximum depth of 1,632m » It is also the world’s largest volume of fresh water 23,000 cubic km. » This means that one-fifth of all the fresh water in the world is located here at Lake Baikal. » Lake Baikal is 640km long and judging by its dimensions only it would be more of a sea than a lake. » Baikal is also the world’s most ancient freshwater lake, it originated 20-25 million years ago. » It is home to many unique species of animals and plants including the freshwater seal. » Lake Baikal is one of the clearest and purest bodies of water. In a good day you could see 40 meters into the lake. » Dimensions of Lake Baikal: It is 636 km long, 79 km wide. » There are 27 islands in Lake Baikal, most of them being uninhabited. » Baikal Lake’s coastline measures 2100 kilometers (around 1300 miles). » More than 300 streams and rivers flow into Lake Baikal, but there is just one outlet, the Angara. » The water in the lake creates a mild microclimate around its shores. » More than half the species found in Lake Baikal are unique to this place.

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Over the past several decades, substantial effort has been invested in the design and development of improved internal combustion engines. Design efforts have been, directed toward the creation of smaller, lighter engines with improved fuel efficiency and power. Engines have been characterized by their method of combustion, e.g., compression (diesel) or spark-ignited (gasoline). Further, engines are described and identified by the orientation and/or number of their pistons and cylinders, e.g., V-8, in-line 6, radial, Wankel rotary, horizontal and horizontally-opposed. Internal combustion engines with horizontally-oriented pistons and cylinders have been the subject of much research over the past several decades. Their inherent low profile offers an opportunity to reduce engine size while maintaining fuel efficiency and power. Various countries have introduced several variations of both four cylinder and six cylinder horizontally-oriented engines. A typical horizontally-oriented engine configuration includes multiple pairs of horizontal cylinders with a separate piston slidably disposed in each separate cylinder. The top or "crown" of each piston, in combination with the cylinder walls and a separate cylinder head, forms a unique, single combustion chamber. Each cylinder head, also provides a separate surface for intake and exhaust valve assemblies. In the case of spark-ignited engines, each cylinder head also provides a port for installation of some means for igniting the combustible mixture, usually a spark plug. For a typical horizontally oriented engine, each piston is connected to a common crankshaft. During operation, a mixture of air and fuel is introduced into each combustion chamber. The mixture is then combusted, by either compression (diesel engines) or a spark (gasoline engines). When combusted, the energy generated by the exothermic expansion of the combustible mixture serves to drive the piston away from the cylinder head. In so doing, the piston's linear kinetic energy is delivered to the engine's crankshaft by a connecting rod rotatably attached to the piston. The crankshaft then delivers rotational power to the power train. Several patents have offered modifications to the typical horizontally-oriented piston and cylinder configuration. Most notably, and of relevance to the present invention, is that prior art which teaches horizontally-oriented engine configurations with one combustion chamber shared between two or more pistons/cylinders. Generally, these types of engines are known as horizontally-opposed engines. For example, Henry (U.S. Pat. No. 1,533,004) teaches an internal combustion engine with a combustion chamber shared between two cylinders. The shared combustion chamber is formed by the walls of two interconnected cylinders, the crowns of two opposing pistons which slidably reciprocate within the cylinders, and a single cylinder head. In addition to acting as a wall of the shared combustion chamber, the cylinder head provides a surface for intake and exhaust ports as well as spark plug access. In Henry, the pistons simultaneously converge toward each other and then simultaneously diverge away from each other during the various engine cycles. Other patents, including most notably Feeback (U.S. Pat. No. 3,485,221), Rassey (U.S. Pat. No. 4,244,338), Johnson (U.S. Pat. No. 4,554,894) and Honkanen (U.S. Pat. No. 5,133,306) have proposed variations on the horizontally-opposed engine configuration. Each of the above include intake and exhaust valve assemblies which are located to the side of each cylinder pair. Consequently, as with Henry discussed above, these engines all require at least one separate cylinder head per cylinder pair. Other relevant prior art teaches internal combustion engines with shared combustion chambers, but whose converging pistons are not horizontally-oriented. For example, Ascari (U.S. Pat. No. 5,447,818) teaches an engine with at least four cylinders that form two separate shared combustion chambers. Two cylinders and pistons are oriented at angles of approximately ninety degrees to each other, with the crown of each piston oriented toward a shared plane of symmetry. Ascari likens his engine to a "superimposed twin V." Again, the shared combustion chamber is formed by the cylinder wall, two piston crowns and a single cylinder head. The prior art clearly evidences that the ability to reduce the overall size and weight of opposed piston engines with shared combustion chambers has been hampered by the need to include a suitable surface, i.e. a cylinder head, to accommodate the shared intake and exhaust valve assemblies. As previously indicated, in engines without shared combustion chambers, each cylinder has a cylinder head which provides a surface for the valve assemblies. Engines with shared combustion chambers have generally provided for the placement of the shared intake and exhaust valve assemblies in a separate "cylinder head-like" element that is separately bolted to the side of the cylinder blocks. The present invention advances the prior art by eliminating the need for a separate cylinder head. Although the prior art teaches reduction in the number of required cylinder heads for dual piston/cylinder engine configurations from two to one, it still struggles with valve design and placement. The intake and exhaust valve assemblies are typically located between the ends of the dual cylinders to serve a common or shared combustion chamber. Consequently, this additional space requirement frequently limited the ability to bring the ends of the cylinders, and hence, the crowns of the pistons, closely together. The patent to Rassey specifically teaches that "previous attempts to adapt poppet valves [in horizontally-opposed engines] have proven largely unsuccessful since the poppet valves cannot be positioned above the piston head as in the more conventional internal combustion engines." Accordingly, a need exists for a cylinder/piston configuration of simple and reliable design which includes a combustion chamber shared between two horizontally-opposed cylinder/piston assemblies, yet allows the use of poppet valve assemblies to service the shared combustion chamber, while eliminating the need for a separate cylinder head to house the valve assemblies, thereby minimizing the size, weight and vertical profile of the engine for equivalent power requirements and providing for smoother, more efficient and less polluting operation.

3.640625

4

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1.. Introduction {#s1} ================ Carbon nanotubes (CNTs) were discovered by Sumio Iijima in 1991 \[[@C1]\] and since then, they have received high attention due to their extraordinary mechanical, electrical and thermal properties. Besides that, CNTs have very low density \[[@C2]\] and very high aspect ratio. CNTs consist of graphene sheets coaxially rolled into hollow cylinders, and can be single-walled or multi-walled depending on the number of graphene sheets. Moreover, CNTs can be metallic or semiconducting depending on the twist of the tubes. In contrast to CNTs, carbon nanofibers (CNFs) comprise cone-shaped graphene layers stacked on top of each other creating completely filled cylinders, which also have excellent mechanical, thermal and electrical properties. At 400 and 7 GPa, the Young modulus and tensile strength of CNFs are higher than those of steel \[[@C3]\]. The thermal conductivity of CNFs (about 1900 W mK^−1^) is five times higher than copper \[[@C4]\] and can carry current density of about 12 MA cm^−2^ which is three times higher than copper \[[@C5], [@C6]\]. CNFs exhibit many significant advantages over CNTs, since they can be grown at lower temperatures and they are 100% metallic, whereas 2/3 of CNTs are semiconducting when grown in bulk \[[@C7]\]. Because of these excellent properties CNFs have potential applications in electrical interconnects \[[@C8]\], as thermal interface materials, as reinforcement additives in polymer composites and as electrodes for supercapacitors. The carbon nanostructures, including CNFs, can be synthesized in several ways including electrospinning, chemical vapor deposition (CVD), laser ablation and arc discharge. There are different types of CVD and these are classified on the basis of energy type used during deposition: microwave plasma enhanced CVD, thermal CVD and direct current plasma enhanced CVD (DC-PECVD) \[[@C9]--[@C11]\]. Depending on the catalyst and the CVD growth method used, different types of carbon nanostructures are obtained. The DC-PECVD method has an advantage over the other growth methods in that it provides high purity and vertical alignment of the produced CNFs \[[@C12]\]. To grow CNFs using CVD, the deposition of catalytic particles on a substrate is required. Transition metals such as iron, cobalt, palladium and nickel are often used as catalysts \[[@C11], [@C13]--[@C15]\]. The catalysts can be deposited in different ways onto the substrate such as deposition of a pure metal film using sputtering or e-beam evaporation techniques and deposition of a nanoparticle (NP)-containing solution via spin coating, dip-coating or spraying methods \[[@C16]--[@C18]\]. The physical vapor deposition (PVD) deposition methods, such as sputtering or evaporation, require expensive equipment, a metal target, clean room laboratory facilities and costly equipment maintenance. In the present study, catalytic palladium NPs are deposited on silicon substrate via spin-coating using highly stable and inexpensive polymer--Pd colloidal solutions. CNFs are then grown on these catalyst particles at complementary metal oxide semiconductor (CMOS) process-compatible temperature thus allowing CNFs to be used in on-chip thermal, electrical and energy storage solutions. Two types of polymer--Pd NPs solutions were used to deposit the palladium catalyst particles: (1) poly(vinylpyrro1idone)-Pd (PVP--Pd) NPs stabilized in methanol solution and (2) poly(lauryl methacrylate)-block-poly(2-(acetoacetoxy)ethyl methacrylate) (LauMA~*x*~-b-AEMA~*y*~/Pd) micellar nanohybrids stabilized in *n*-hexane. Different types of polymers are used due to their different thermal stabilization temperatures. The polymers are stable up to certain temperature and burn off when heated to higher temperature thus leaving Pd NPs on the surface of the substrate. The stabilization temperature of LauMA~*x*~-b-AEMA~*y*~ and PVP polymers is around 200 °C and 400 °C respectively \[[@C19]\]. The synthesis and characterization of the aforementioned polymer-stabilized Pd NPs has been reported in other studies \[[@C20]--[@C23]\]; however, in this work these polymer-metal nanohybrids have been employed for the growth of CNFs. The use of such catalyst-containing solutions is advantageous since those are nontoxic, cheap and can be easily prepared using low-cost wet-chemistry procedures. In addition, their deposition onto selected substrates does not require the use of expensive equipment. Moreover, the polymers can be easily washed away and the substrate can be reused in case of process failure during NPs deposition. This is a rapid and industry compatible deposition method that can be used to grow a film of CNFs at the backside of a chip for heat sink applications. Three different PVP--Pd nanohybrid solutions were prepared in methanol, in which the polymer content was kept constant and only the palladium content varied. In the case of the LauMA~*x*~-b-AEMA~*y*~/Pd micellar systems stabilized in *n*-hexane, two different block copolymers (polymer A: *x* = 120, *y* = 67; polymer B: *x* = 50, *y* = 9) are employed as the palladium NPs stabilizing agents. The CNFs were grown using the DC-PECVD technique at different temperatures i.e. at a high temperature (550 °C), at a CMOS compatible temperature (390 °C) and even at 40 °C lower (350 °C). The specific capacitance and cyclability of the CNFs were measured using cyclic voltammetry to demonstrate the electrical properties and applicability of these nanostructures as supercapacitor electrodes directly built on CMOS chips. 2.. Fabrication, characterization and measurements {#s2} ================================================== The synthetic methodologies followed for the preparation of the PVP--Pd and the LauMA~*x*~-b-AEMA~*y*~-Pd hybrid solutions are described below.(1)A typical synthetic methodology followed for the synthesis of the PVP--Pd nanohybrid colloidal systems (moles vinyl pyridine units/moles palladium salt = 9:1) is described as follows \[[@C19], [@C23]\]: in a round bottom flask equipped with a magnetic stirrer, PVP (1 g, 9 × 10^−3^ moles of vinylpyrridine units) (Sigma-Aldrich, MW = 1300 000) was dissolved in methanol (10 mL). Subsequently, palladium acetate (0.22 g, 1 × 10^−3^ moles) (Pd(OAc)~2~, Sigma-Aldrich, 98%) was added to the polymer solution and the reaction flask was placed under reflux for 2 h. During this period, the color of the solution changed from yellow to dark brown indicating the formation of palladium NPs. After the completion of the reaction, the brown-colored solution was left to cool down to room temperature and it was then stored in sealed glass vials. The solutions were highly stable and no precipitation was observed even after several months.The above-mentioned methodology was employed for synthesizing two more PVP--Pd nanohybrid colloidal systems stabilized in methanol, in which the polymer content was kept the same and only the metallic (Pd) content varied i.e. the molar ratio of the vinyl pyridine units to the palladium salt was 18:1 and 38:1.(2)The Pd-containing LauMA~*x*~-b-AEMA~*y*~ micellar hybrids have been prepared in *n*-hexane by following a previously reported methodology \[[@C20], [@C22]\]. Exemplarily, the procedure followed for the synthesis of the LauMA~120~-b-AEMA~67~/Pd micellar nanohybrids is described as follows: LauMA~120~-b-AEMA~67~ (20 mg, 0.03 mmoles of AEMA units) was dissolved in *n*-hexane (5 mL). After complete dissolution of the polymer, triethylamine (0.021 mL, 0.15 mmoles ) was added. Subsequently, the polymer solution was transferred into a glass vial containing Pd(OAc)~2~ (3.40 mg, 0.015 mmoles) and the mixture was left to stir at room temperature until complete solubilization of the salt. Upon complexation and solubilization, the color of the solution changed from white to yellow transparent. Finally, the reducing agent namely hydrazine monohydrate (1.46 *μ*L, 0.03 mmoles) was added to the solution upon stirring. This was accompanied by a color change of the solution from yellow to dark brown indicating the reduction of palladium (II) ions into metallic palladium (0) NPs. The resulting solution was left to stir for 24 h at room temperature. The size of the palladium NPs generated within the micellar cores has been already reported \[[@C22]\]. The average diameter of the palladium NPs is 2.3 ± 0.3 nm for the LauMA~50~-b-AEMA~9~/Pd(solution A) and 8.8 ± 1.7 nm for LauMA~120~-b-AEMA~67~/Pd(solution B). A 2 inch n-type silicon wafer was used as a substrate for the uniform deposition of the polymer-palladium solutions. Titanium/titanium nitride (Ti/TiN) of thicknesses 50 and 100 nm were sputtered on each side of the chip using FHR MS 150 sputter machine in order to have better electrical contact between back and front side of the sample, because of backside probing of the chip for measurements. The polymer-palladium NPs solutions were later spun using standard resist spinners. Vertically aligned CNFs were grown at different temperatures by the DC-PECVD method as described in \[[@C8], [@C24]\]. A mixture of acetylene and ammonia gases was used where the acetylene is the source gas and the ammonia is a carrier gas. The growth was executed for 2 h on all samples. The temperature of the heater is measured and regulated during the whole growth process to an accuracy of ±2° using a built-in thermocouple inside the grounded heating plate. The chips were weighed before the deposition of the palladium NPs and after the growth of CNFs for determining the weight of the CNFs including catalyst, a parameter used in evaluating the capacitance per gram of such electrodes. The weight measurements were performed using a high precision balance 'Sartorius Analytical Balance BP211D' with a resolution of 10 *μ*g. Transmission electron microscopy (TEM) analysis performed on the LauMA~*x*~-b-AEMA~*y*~/Pd (solution A) system was carried out on a 1010 JEOL microscope (200 kV). The suspension of MNPs was dried on a carbon coated copper grid to allow the TEM investigation. The scanning electron microscopy (SEM) analysis of the CNFs was conducted using JEOL JSM-6301F. In order to see the morphology of the CNFs, images were taken at 40° tilt angle as well as top view images at zero tilt. Cyclic voltammetry (CV) was performed to evaluate the capacitance. A three electrode setup was used with a silver/silver chloride (Ag/AgCl) electrode as the reference electrode and platinum mesh as the counter electrode. The electrolyte used was 1M KOH (99.99%, Aldrich). The limit of measuring the electrode cell was one centimeter diameter disk. The samples were mounted and dipped in the electrolyte solution for a few minutes while nitrogen gas was blowing to wet the CNFs. The CV curve was obtained using Gamry Instruments Reference 600 (Framework 6.1). The voltage sweep ranging from −0.2 to 0.3 V was applied and different voltage scan rates were used. The voltammetry using 10 mV s^−1^ scan rate was carried out for 18 cycles to exclude the doubt of initial surface reactions whereas 5 cycles were run for other scan rates. The same measurement was also performed for 1000 cycles to measure the cyclability at 20 mV s^−1^ scan rate while keeping the other parameters the same. The ideal double layer capacitance behavior is the rectangular shape of the voltammetry characteristics drawn between current and voltage \[[@C25]\]. 3.. Results and discussion {#s3} ========================== Information on the palladium NPs content (provided as the molar ratio of the metal-binding units of the polymer to the palladium salt precursor), growth temperature, weight of CNFs and capacitance is provided in table [1](#TB1){ref-type="table"}, whereas the specific capacitance measured at different voltage scan rates is given in table [2](#TB2){ref-type="table"}. ###### Properties of the CNFs grown using different polymer-palladium NPs solutions at different temperatures, their capacitance and specific capacitance mF cm^−2^ (per footprint area). \[vinyl pyridine\]/\[Pd(OAc)~2~\] Growth temperature (°C) Weight (*μ*g) Length (*μ*m) Capacitance (mF) Specific capacitance (mF cm^−2^) ----------------------------------- ------------------------- --------------- --------------- ------------------ ---------------------------------- Bare chip 0.1 0.12 38:1 550 53 14 0.8 1 18:1 550 245 9 3.1 4 9:1 550 916 5 7.1 9 9:1 390 612 1 2.6 3.3 \[AEMA\]/\[Pd(OAc)~2~\] \[LauMA~120~-b-AEMA~67~\] 2:1 390 654 1 2.1 2.7 \[LauMA~50~-b-AEMA~9~\] 2:1 390 115 2 1.4 1.8 \[LauMA~120~-b-AEMA~67~\] 2:1 350 250 1.4 3.1 4 \[LauMA~50~-b-AEMA~9~\] 2:1 350 115 1.6 0.2 0.2 ###### Specific capacitance mF cm^−2^ (per footprint area) measured at different voltage scan rates. \[vinyl pyridine\]/\[Pd(OAc)~2~\] *T* (°C) 10 mV s^−1^ 20 mV s^−1^ 50 mV s^−1^ 100 mV s^−1^ ----------------------------------- ---------- ------------- ------------- ------------- -------------- PVP/Pd 38:1 550 1 0.8 0.7 0.6 PVP:Pd 18:1 550 4 2.4 1.6 1.2 PVP/Pd 9:1 550 9\. 6 4.6 4 PVP/Pd 9:1 390 3.3 2.6 2 2 \[AEMA\]/\[Pd(OAc)~2~\] Solution A 350 0.2 0.2 0.15 0.14 Solution B 390 2.7 2 1.5 1.3 Solution B 350 4 3 2.3 2 Solution A 390 1.8 1.41 1.1 1 A representative TEM image of the solution A system is provided in figure [1](#F1){ref-type="fig"}. As seen in the image, tiny, spherical palladium NPs can be visualized with average diameters in the range 2.3 ± 0.3 nm. The presence of a few larger aggregates may be due to drying-induced aggregation during TEM sample preparation. In the case of the PVP/Pd systems, HRTEM analysis revealed that the palladium NPs are nanocrystals with average diameters below 10 nm. The crystalline planes (111) and (200) of palladium NP could be visualized with characteristic interplanar distances of 2.27 and 1.97 Å, respectively \[[@C26]\]. Tilted view and top view (inset on each picture) SEM images of CNFs grown at 550 °C using three PVP/Pd solutions having different metallic (palladium) content are shown in figures [2](#F2){ref-type="fig"}(a)--(c) whereas SEM images of the CNFs grown at 390 °C using the PVP/Pd (1:9) solution is provided in figure [2](#F2){ref-type="fig"}(d). ![TEM image of the LauMA~50~-b-AEMA~9~/Pd system (solution A).](TSTA1166125201){#F1} ![SEM images of CNFs grown by DC-PECVD for 2 h at different temperatures on palladium NPs using various PVP--Pd colloidal solutions given as (a) PVP:Pd 38:1, growth at 550 °C. (b) PVP:Pd 18:1, growth at 550 °C. (c) PVP:Pd 9:1, growth at 550 °C. (d) PVP:Pd 9:1, growth at 390 °C.](TSTA1166125202){#F2} Similarly, the tilted view and top view (inset on each picture) SEM images of the CNFs grown at 390 and 350 °C using solution A and solution B are shown in figures [3](#F3){ref-type="fig"}(b), (d) and (a), (c). ![SEM images of CNFs grown by DC-PECVD for 2 h on two different LauMA~*x*~-b-AEMA~*y*~/Pd micellar solutions at different temperatures given as (a) LauMA~120~-b-AEMA~67~/Pd (solution B) growth at 390 °C. (b) LauMA~50~-b-AEMA~9~/Pd (solution A) growth at 390 °C. (c) LauMA~120~-b-AEMA~67~/Pd (solution B) growth at 350 °C. (d) LauMA~50~-b-AEMA~9~/Pd (solution A) growth at 350 °C.](TSTA1166125203){#F3} It is clear from the SEM images that the CNFs grown at lower temperature 350 °C are vertically aligned similar to those grown at the highest temperature (550 °C) as shown in figures [2](#F2){ref-type="fig"} and [3](#F3){ref-type="fig"}. In addition, inset of figures [2](#F2){ref-type="fig"} and [3](#F3){ref-type="fig"} also show the uniform growth of CNFs confirming the uniform deposition of palladium catalyst NPs using spin-coating, which is in line with \[[@C26]\]. Moreover, in the case of the PVP--Pd systems, the CNF density increases significantly by increasing the palladium content within the PVP--Pd colloidal hybrid solutions i.e. from 38:1 to 18:1 and to 9:1 (figures [2](#F2){ref-type="fig"}(a)--(c) respectively) thus resulting in an increase in CNF weight, as shown in table [1](#TB1){ref-type="table"}. In addition, SEM analysis also reveals that under identical growth conditions, the CNFs grown using the highest palladium-containing system (9:1) are shorter in length compared to those grown using the lowest palladium-containing system (38:1). By using the same palladium-containing system (9:1) the CNFs grown at higher (550 °C) temperatures are much longer than those grown at 390 °C, in line with the weight measurements, although less dense than the CNFs grown at 390 °C. In the case of the LauMA~*x*~-b-AEMA~*y*~/Pd solutions, the average diameter of the palladium nanocatalyst is 2.3 ± 0.3 nm for solution A and 8.8 ± 1.7 nm for solution B. Despite their size differences both systems are found within the optimum size range enabling CNF growth at a low temperature (350 °C) as seen in the SEM images provided in figures [3](#F3){ref-type="fig"}(c) and (d). The top view SEM images (inset in figure [3](#F3){ref-type="fig"}) clearly show that under identical growth temperature, the CNFs grown using solution B are denser and heavier than those grown using solution A, but shorter in length compared to those obtained from solution A, as shown in table [1](#TB1){ref-type="table"}. Furthermore, when the growth is performed at different temperatures, solution B gives longer but less dense CNFs at low temperature 350 °C. On the other hand, solution A gives denser and shorter CNFs at the same growth temperature. The CV curves for the electrical characterization of the CNFs grown using the PVP--Pd and the LauMA~*x*~-b-AEMA~*y*~-Pd solutions are provided in figures [4](#F4){ref-type="fig"}(a), (b) and [5](#F5){ref-type="fig"}(a). The specific capacitance (mF cm^−2^ footprint area) curves measured at difference voltage scan rate are shown in figures [4](#F4){ref-type="fig"}(c) and [5](#F5){ref-type="fig"}(b). The cyclability curves for 1000 cycles are shown in figures [4](#F4){ref-type="fig"}(d) and [5](#F5){ref-type="fig"}(c) whereas magnified images of the last 20 cycles from 980 to 999 are shown in figures [4](#F4){ref-type="fig"}(e) and [5](#F5){ref-type="fig"}(d). ![Cyclic voltammetry curves of CNFs. (a) At 550 °C using different PVP--Pd solutions with different palladium content. (b) At 550 °C and 390 °C using PVP:Pd 9:1solution. (c) Specific capacitance (mF cm^−2^ foot print area) versus voltage scan rate. (d) Cyclability of CNFs grown at 550 °C and 390 °C using PVP:Pd 9:1 solution (normalized by specific capacitance of first cycle). (e) Cycles from 975 to 999.](TSTA1166125204){#F4} ![(a) Cyclic voltammetry curves of CNFs grown using solution A and solution B at 350 °C and 390 °C. (b) Specific capacitance (mF cm^−2^ foot print area) versus voltage scan rate. (c) Cycle life of solution B (normalized by specific capacitance of first cycle). (d) Cycles from 980 to 999.](TSTA1166125205){#F5} The voltammograms given in figures [4](#F4){ref-type="fig"}(a), (b) and [5](#F5){ref-type="fig"}(a) are fairly rectangular showing the double layer capacitive behavior of the CNFs obtained using both types of polymer--Pd catalyst solutions, however, the peaks at extreme sweep voltages show some pseudocapacitive charge storage which may arise from the reaction of underlayer with aqueous electrolyte. At 550 °C growth temperature and 10 mV s^−1^ scan rate, the specific capacitance (per cm^−2^ foot print area) is larger (9 mF cm^−2^) for higher concentration (9:1) of palladium NPs in the PVP--Pd solution and lower (1 mF cm^−2^) for lower concentration (38:1) confirming the active capacitive role of CNFs. In fact, shorter but denser CNFs for the (9:1) solution give a higher surface area accessible to electrolyte than longer but less dense CNFs for the (38:1) solution, and the higher surface area results in higher current on voltammogram and hence higher specific capacitance as shown in figure [4](#F4){ref-type="fig"}(a) and table [1](#TB1){ref-type="table"}. In addition the specific capacitance is 3.3 mF cm^−2^ for the CNFs grown at 390 °C using the PVP--Pd (9:1) solution. In the case of the LauMA~*x*~-b-AEMA~*y*~/Pd solutions the specific capacitance is higher (2.7 and 4 mF cm^−2^) for CNFs synthesized using solution B than solution A when grown at corresponding temperatures 350 °C and 390 °C which is in line with the weight of the CNFs. Moreover, for the same solution, the longer CNFs give a higher surface area which results in higher current on the voltammogram and hence higher specific capacitance, as shown in figure [5](#F5){ref-type="fig"}(a) and table [1](#TB1){ref-type="table"}. The capacitive behavior indicates the similar electrical behavior of CNFs grown at both low and high temperatures. The specific capacitance at 100 mV s^−1^ ranges from 3.9 to 0.140 mF cm^−2^. This specific capacitance is many folds higher than the recently reported capacitance obtained from the CVD grown vertically aligned CNFs \[[@C27]\]. Furthermore, the maximum specific capacitance at 100 mV s^−1^ scan rate is 3.9 mF cm^−2^ obtained from the CNFs grown at 550 °C, table [2](#TB2){ref-type="table"}, which is almost equal to the maximum reported capacitance obtained from graphene-CNT based microcapacitors (3.93 mF cm^−2^) synthesized on a similar silicon substrate but using a longer voltage scan range \[[@C28]\]. Moreover, the specific capacitance obtained from CNFs grown at low temperature 350 °C and 390 °C, table [2](#TB2){ref-type="table"}, is 1.9--2 mF cm^−2^, half of the reported specific capacitance mentioned above, nevertheless the growth temperature of CNFs here is below the CMOS process-compatible temperature. In addition, the cyclic voltammetry at different voltage scan rates shows that specific capacitance decreases by increasing the scan rate from 10 to 100 mV s^−1^ for both polymer--Pd types used, figures [4](#F4){ref-type="fig"}(c) and [5](#F5){ref-type="fig"}(b), due to a kinetically slow faradaic reaction on the electrode surface which does not take place at high scan rate[^5^](#stam508704fn1){ref-type="fn"} [^1]. Moreover, the cycle life curves of both polymer--Pd solution types show the decrease in specific capacitance with increase in cycles, figures [4](#F4){ref-type="fig"}(d) and [5](#F5){ref-type="fig"}(c), which eventually becomes uniform and remains unchanged as shown in the plots of the last 20 cycles, given in figures [4](#F4){ref-type="fig"}(e) and [5](#F5){ref-type="fig"}(d). The more than 90% capacitance retention for CNFs grown from the PVP--Pd solution and 80% for the CNFs grown from solution B after 1000 cycles of cyclic voltammetry proves the long cycle life of these materials as supercapacitor electrodes. Due to the lower density of CNFs for solution B the electrolyte damages the metal underlayer in between the CNFs thus resulting in lower capacitance after 1000 cycles. The above results indicate that the CNFs grown from all types of polymer-stabilized Pd nanocatalysts are vertically aligned similar to CNFs grown from a PVD deposited catalyst film. Moreover the density and weight of the CNFs grown from a PVP--Pd solution can be controlled by controlling the palladium contents in the PVP--Pd solution in the tested concentration range. Furthermore CNFs of different diameters can be grown from LauMA~*x*~-b-AEMA~*y*~/Pd solutions. Finally, the electrical characterization proves that electrical properties of all the CNFs are the same; however, the low capacitance in solution A is due to the lower density of CNFs in the footprint area. The CNF growth performed at this temperature has created the opportunity to grow the CNFs directly on CMOS chips. The possibility of CNF growth at temperatures lower (350 °C) than CMOS temperature ensures their usage even if the CMOS temperature drops further. 4.. Conclusions {#s4} =============== Catalytic palladium NPs of various sizes were deposited on a silicon substrate via spin-coating using two types of highly stable and cost-effective polymer--Pd colloidal solutions. More precisely, PVP or methacrylate-based diblock copolymers of the type LauMA~*x*~-b-AEMA~*y*~ were employed as steric stabilizers for palladium NPs in organic solvents. Vertically aligned CNFs were synthesized on these palladium nanocatalysts using the direct plasma enhanced CVD technique at different temperatures ranging from 550 °C down to 350 °C, which can be considered as a CMOS-compatible temperature. The SEM characterization had shown that the CNFs grown at low temperature were vertically aligned similar to those generated at high temperature. The capacitive behavior and long cyclability had proven not only the suitability of the as-grown CNFs as electrodes for supercapacitors but also that the CNFs grown at low and high temperatures had similar electrical behavior. We have demonstrated a CMOS compatible process to build efficient heat sink, interconnects or supercapacitor electrodes directly on the chip based on vertically aligned CNFs as the active material. This work has been performed within the MNT-ERA.NET Carpolcap project supported by Vinnova, the Swedish Governmental Agency for Innovation Systems and the Cyprus Research Promotion Foundation (Grant No. KOINA/MNT-ERA.NET/0311/01). The authors thank Dr Rodica Paula Turcu (National Institute for Isotopic and Molecular Technologies, Cluj-Napoca, Romania) for performing the TEM characterization on the LauMA~50~-b-AEMA~9~/Pd system and Dr Maria Demetriou for the synthesis of the LauMA-b-AEMA block copolymers used in the present study. [^1]: [www.gamry.com/application-notes/testing-electrochemical-capacitors-part-1-cyclic-voltammetry-and-leakage-current/](http://www.gamry.com/application-notes/testing-electrochemical-capacitors-part-1-cyclic-voltammetry-and-leakage-current/), accessed successfully on 06-10-2014.

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eso1544 — Science Release The Glowing Halo of a Zombie Star VLT maps out remains of white dwarf’s meal The remains of a fatal interaction between a dead star and its asteroid supper have been studied in detail for the first time by an international team of astronomers using the Very Large Telescope at ESO’s Paranal Observatory in Chile. This gives a glimpse of the far-future fate of the Solar System. Led by Christopher Manser, a PhD student at the University of Warwick in the United Kingdom, the team used data from ESO’s Very Large Telescope (VLT) and other observatories to study the shattered remains of an asteroid around a stellar remnant — a white dwarf called SDSS J1228+1040 [1]. Using several instruments, including the Ultraviolet and Visual Echelle Spectrograph (UVES) and X-shooter, both attached to the VLT, the team obtained detailed observations of the light coming from the white dwarf and its surrounding material over an unprecedented period of twelve years between 2003 and 2015. Observations over periods of years were needed to probe the system from multiple viewpoints [2]. “The image we get from the processed data shows us that these systems are truly disc-like, and reveals many structures that we cannot detect in a single snapshot,” explained lead author Christopher Manser. The team used a technique called Doppler tomography — similar in principle to medical tomographic scans of the human body — which allowed them to map out in detail the structure of the glowing gaseous remains of the dead star’s meal orbiting J1228+1040 for the first time. While large stars — those more massive than around ten times the mass of the Sun — suffer a spectacularly violent climax as a supernova explosion at the ends of their lives, smaller stars are spared such dramatic fates. When stars like the Sun come to the ends of their lives they exhaust their fuel, expand as red giants and later expel their outer layers into space. The hot and very dense core of the former star — a white dwarf — is all that remains. But would the planets, asteroids and other bodies in such a system survive this trial by fire? What would be left? The new observations help to answer these questions. It is rare for white dwarfs to be surrounded by orbiting discs of gaseous material — only seven have ever been found. The team concluded that an asteroid had strayed dangerously close to the dead star and been ripped apart by the immense tidal forces it experienced to form the disc of material that is now visible. The orbiting disc was formed in similar ways to the photogenic rings seen around planets closer to home, such as Saturn. However, while J1228+1040 is more than seven times smaller in diameter than the ringed planet, it has a mass over 2500 times greater. The team learned that the distance between the white dwarf and its disc is also quite different — Saturn and its rings could comfortably sit in the gap between them [3]. The new long-term study with the VLT has now allowed the team to watch the disc precess under the influence of the very strong gravitational field of the white dwarf. They also find that the disc is somewhat lopsided and has not yet become circular. “When we discovered this debris disc orbiting the white dwarf back in 2006, we could not have imagined the exquisite details that are now visible in this image, constructed from twelve years of data — it was definitely worth the wait,” added Boris Gänsicke, a co-author of the study. Remnants such as J1228+1040 can provide key clues to understanding the environments that exist as stars reach the ends of their lives. This can help astronomers to understand the processes that occur in exoplanetary systems and even forecast the fate of the Solar System when the Sun meets its demise in about seven billion years. Notes [1] The white dwarf’s full designation is SDSS J122859.93+104032.9. [2] The team identified the unmistakable trident-like spectral signature from ionised calcium, called the calcium (Ca II) triplet. The difference between the observed and known wavelengths of these three lines can determine the velocity of the gas with considerable precision. [3] Although the disc around this white dwarf is much bigger than Saturn’s ring system in the Solar System, it is tiny compared to the debris discs that form planets around young stars. More information This research was presented in a paper entitled “Doppler-imaging of the planetary debris disc at the white dwarf SDSS J122859.93+104032.9”, by C. Manser et al., to appear in the Monthly Notices of the Royal Astronomical Society. The team is composed of Christopher Manser (University of Warwick, UK), Boris Gaensicke (University of Warwick), Tom Marsh (University of Warwick), Dimitri Veras (University of Warwick, UK), Detlev Koester (University of Kiel, Germany), Elmé Breedt (University of Warwick), Anna Pala (University of Warwick), Steven Parsons (Universidad de Valparaiso, Chile) and John Southworth (Keele University, UK). ESO is the foremost intergovernmental astronomy organisation in Europe and the world’s most productive ground-based astronomical observatory by far. It is supported by 16 countries: Austria, Belgium, Brazil, the Czech Republic, Denmark, France, Finland, Germany, Italy, the Netherlands, Poland, Portugal, Spain, Sweden, Switzerland and the United Kingdom, along with the host state of Chile. ESO carries out an ambitious programme focused on the design, construction and operation of powerful ground-based observing facilities enabling astronomers to make important scientific discoveries. ESO also plays a leading role in promoting and organising cooperation in astronomical research. ESO operates three unique world-class observing sites in Chile: La Silla, Paranal and Chajnantor. At Paranal, ESO operates the Very Large Telescope, the world’s most advanced visible-light astronomical observatory and two survey telescopes. VISTA works in the infrared and is the world’s largest survey telescope and the VLT Survey Telescope is the largest telescope designed to exclusively survey the skies in visible light. ESO is a major partner in ALMA, the largest astronomical project in existence. And on Cerro Armazones, close to Paranal, ESO is building the 39-metre European Extremely Large Telescope, the E-ELT, which will become “the world’s biggest eye on the sky”. Links Contacts Christopher Manser University of Warwick United Kingdom Email: C.Manser@warwick.ac.uk Boris Gänsicke University of Warwick United Kingdom Tel: +44 (0)2476574741 Email: Boris.Gaensicke@warwick.ac.uk Tom Frew International Press Officer, University of Warwick United Kingdom Tel: +44 (0)24 7657 5910 Cell: +44 (0)7785 433 155 Email: a.t.frew@warwick.ac.uk Richard Hook ESO Public Information Officer Garching bei München, Germany Tel: +49 89 3200 6655 Cell: +49 151 1537 3591 Email: rhook@eso.org Connect with ESO on social media

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Quantum teleportation provides a means to transport an unknown quantum state from one location to another over arbitrary distances. Since originally being proposed in 1993[@b1], the study on quantum teleportation has aroused great interest. Its experimental realizations in various different ways have been reported. For instance, the best known methods have been implemented using photon polarization and optical techniques[@b2][@b3], by means of squeezed states of light[@b4], by applying nuclear magnetic resonance (NMR) techniques[@b5], and by a hybrid technique[@b6][@b7]. Teleportation has also been accomplished between photons and a single atomic ensemble[@b8][@b9], between distant atomic objects[@b10][@b11][@b12][@b13], and in a chip-based superconducting circuit architecture[@b14]. Quantum teleportation is essential for large-scale quantum communication[@b15][@b16][@b17] and distributed quantum networks[@b18]. It has proven to be a useful tool for realizing universal quantum logic gates in quantum computing and general quantum information manipulation[@b19]. However, all protocols for accomplishing quantum teleportation require non-local correlations, or Einstein--Podolsky--Rosen (EPR) entanglement, between systems shared by the sender and receiver. On the other hand, non-separable correlations among two or more different degrees of freedom from the same classical optical beam, have been discussed[@b20][@b21][@b22][@b23][@b24][@b25][@b26][@b27][@b28][@b29][@b30][@b31][@b32]. The violation of Bell\'s inequality or GHZ theorem for such a non-separable correlation has been demonstrated experimentally[@b20][@b21][@b22][@b23][@b24][@b25]. Thus, a non-separable classical correlation is called "nonquantum entanglement" or "classical entanglement"[@b25][@b26][@b27][@b28][@b29][@b30]. Such a classical entanglement has been applied to resolve basic issues in polarization optics[@b25], simulate quantum walks, et al.[@b27]. The investigations have shown that quantum optical procedures requiring entanglement without non-locality can actually be achieved in classical optics regime[@b25][@b26][@b27][@b28][@b29][@b30][@b31][@b32]. Recently, some discussions on the non-local classical optical correlation of two coherent light beams have been done[@b33][@b34][@b35][@b36]. Some studies, which have attempted to simulate the quantum teleportation by classical optics, have been performed[@b29][@b30][@b31]. However, the classical correspondence on the true meaning of quantum teleportation, which is based on the classical EPR correlation state, has not been achieved. In this work, we present a new method to construct a non-local classical EPR correlation state by using two incoherent light beams and implement a classical analogy on the true meaning of quantum teleportation. Results and Discussion ====================== Non-local classical optical correlation --------------------------------------- Initially two independent light beams, *E*~1~ and *E*~2~ with different wavelengths, are considered and pass through a 50/50 beam splitter (BS) as shown in [Fig. 1](#f1){ref-type="fig"}. The fields of two light beams satisfy complete incoherent condition and . Here and *t* represent coordinates of space and time. After the BS and a half-wave plate (HWP) in one output of the BS, two new outputs with and can be obtained, where and refer to the horizontal and vertical polarization components, respectively. In order to analyze the correlation properties between and , a half-wave plate (HWP) and a polarizing beam splitter (PBS) are introduced in each path. They function to rotate angles of the light beam and separate and polarized light. Here *θ~a~* and *θ~b~* represent polarization rotated angles in two paths, respectively. After the HWP and PBS, two polarized beams become four beams. Their fields are described by *E~ah~*, *E~av~*, *E~bh~* and *E~bv~*, respectively, which can be modulated by *θ~a~* and *θ~b~*. Now we perform the famous Clauser--Horne--Shimony--Holt (CHSH) test in our system as shown in [Fig. 1](#f1){ref-type="fig"}. The correlation function is defined in the following form[@b20]:where *P~HH~* = *N~HH~* (*θ~a~*,*θ~b~*)/*N~Total~*, *P~VV~* = *N~VV~* (*θ~a~*,*θ~b~*)/*N~Total~*, *P~HV~* = *N~HV~* (*θ~a~*,*θ~b~*)/*N~Total~*, and *P~VH~* = *N~VH~* (*θ~a~*,*θ~b~*)/*N~Total~* are normalized correlated probabilities when polarizations of each beam are measured, and *N~Total~* = *N~HH~* (*θ~a~*,*θ~b~*) + *N~VV~* (*θ~a~*,*θ~b~*) + *N~HV~* (*θ~a~*,*θ~b~*) + *N~VH~* (*θ~a~*,*θ~b~*). In our experiment, such correlated probabilities can be represented by the first order correlation of electric fields through *N~IJ~* (*θ~a~*,*θ~b~*) (I(J) represents H or V):In the experiment the fields of output lights are not directly measured. However, the first-order field correlation can be obtained through measuring the difference of light intensities at two export positions on Mach-Zehnder interferometer, because . Here *I*~1~ and *I*~2~ represent the light intensities at two export positions of the Mach-Zehnder interferometer and Δ*I* is the difference between them. More information about the measurement method for the first-order field correlation is provided in the Methods section. [Figure 2](#f2){ref-type="fig"} shows experimental results for the correlation functions *C*(*θ~a~*,*θ~b~*) as a function of polarization rotated angle *θ~a~* at some certain *θ~b~*. Here two laser beams (continuous wave mode) with different wavelengths, 532 *nm* and 632.8 *nm*, are used. Their intensities are taken as 2 mW. The circle dots and solid lines represent the experimental measurements and theoretical results, respectively. It can be seen that the experimental results are in good agreement with the theoretical calculations. After we have obtained *C*(*θ~a~*,*θ~b~*), the CHSH formulation of Bell\'s measurement is used to quantify such correlation. The CHSH measurement isIt is well known that the local realism theories give \|*B*\| \< 2. However, from the experimental results marked by dashed lines in [Fig. 2](#f2){ref-type="fig"}, *B* = 2.597 ± 0.012 \> 2 is obtained as *θ~a~* = *π*/4, *θ~b~* = 0, and . The presented experiment yields the strongest violation of Bell\'s inequalities. Any of the four EPR-Bell states can be constructed by adjusting polarization and phase factor via HWP in the above experimental setup. This is highly similar to the production of polarization-entangled photon pairs from spontaneous down-conversion of nonlinear crystals[@b37]. For example, the output fields and shown in [Fig. 1](#f1){ref-type="fig"} correspond to the following symmetric Bell-state:Here we use the notation \|*h*)*~i~*(\|*v*)*~i~*) to express a classical state[@b29][@b31]. That is to say, if polarization is measured in one beam, the information of polarization can be "determined" in another beam due to the first-order field correlation, and vice versa. This means that a classical correlation state has been constructed. Because the correlation between two beams is independent on the separation between them, such a correlation is non-local and can be regarded as a classical analogy of EPR entangled state in quantum mechanics. The problem is whether or not some unique phenomena such as quantum teleportation can be realized by applying such a classical EPR correlation state, which is similar to the case in quantum information process. Classical analogy of quantum teleportation based on non-local classical correlation ----------------------------------------------------------------------------------- In order to study the classical analogy of quantum teleportation, the experimental setup shown in [Fig. 3](#f3){ref-type="fig"} is considered. The experimental generation of EPR correlation states and Bell-state measurement are two key parts in the teleportation scheme. In this scheme, above classical EPR correlation states are used as the source. A three-photon scheme is referred to for the Bell-state measurement as described by D. Bouwmeester et. al.[@b2]. This system features the antisymmetric state obtained from four Bell-states. Thus, the antisymmetric Bell-state is used in our teleportation scheme: . This corresponds to and in our classical EPR system, which are shared by Alice and Bob, for example. If Alice want to teleport an initial state \|*ψ~c~*) = *c*~1~ \|*h*) + *c*~2~ \|*v*) to Bob, she needs perform a joint Bell-state measurement on the initial state and . In the experiments, the field corresponding to the initial state \|*ψ~c~*) is expressed as: , where , *c*~1~ and *c*~2~ satisfy \|*c*~1~\|^2^ + \|*c*~2~\|^2^ = 1. When *c*~1~ and *c*~2~ are considered real, corresponds to the linear polarization case. Whereas, when *c*~1~ and *c*~2~ are complex, it is in correspondence to the circular polarization case. We first consider linear polarization case, in which *c*~1~ and *c*~2~ can be expressed by the direction angle of polarization *θ*: *c*~1~ = cos *θ* and *c*~2~ = sin *θ*. Thus, *θ* will be the teleported information. In order to perform a joint Bell-state measurement on the initial state and , an optical element group is constructed that includes a BS and two HWPs as shown in [Fig. 3](#f3){ref-type="fig"}. There are two output ports of the BS, in which one is the sum of two input fields, and the other is the difference of the two. Two HWPs are placed at the output port of the difference. The functions of two HWPs are to realize interchange between and polarizations, and add a *π* phase for the component of polarization field. For such an optical element group, if the input ports are in the Bell-states, it is easy to demonstrate by the correlation measurement of the first-order field that only the output of the antisymmetric state is not zero, and the outputs of three symmetric states all are zero (see Methods section). This is similar to the scheme of the Bell measurements in Ref. [@b2]. Referring back to the previous example, and considering synchronicity of Alice\'s and Bob\' measurements, Alice obtains the information *E~ac~* as and enter the optical element group, and then sends it to Bob through the classical channel. Here *E~ac~* represents the amplitude of field without any polarization information (see [Supplementary](#s1){ref-type="supplementary-material"}). Owing to lack of technique to measure fields, we had to send the beam to Bob in the experiment. Next, we show that Bob can only use the coherence property of the field rather than the polarization information, and such a process is corresponded to the method used in Ref. [@b2]. After Bob receives the information that Alice sent, he will perform the correlation measurement of the first-order field by using the information and in order to obtain the teleported material. This is because there is a strong correlation between *E~ac~* and (see [Supplementary](#s1){ref-type="supplementary-material"}). For example, as passes through a rotated PBS, it will be orthogonally decomposed into *E*~//~ and as shown in [Fig. 3](#f3){ref-type="fig"}. Our theoretical calculations show that \|〈*E~ac~E*~//~〉\|^2^ = cos^2^ (*θ* − *ϕ*) and , which are the correlation of field without polarization (see [Supplementary](#s1){ref-type="supplementary-material"}). Here *ϕ* represents the rotated angle of the PBS, and is taken as 0° when the polarization of transmission fields is horizontal. From these relations, it is not difficult to find that *θ* and *ϕ* are in one-to-one correspondence. If Bob has obtained the maximum of the first-order correlation between *E~ac~* and *E~//~* for a polarization direction, the corresponding *ϕ* for such a polarization direction is the teleported information *θ* (see [Supplementary](#s1){ref-type="supplementary-material"}). In the experiment, the first-order correlations between *E~ac~* and *E~//~* () are measured by the difference of light intensities, which is similar to the above method for testing CHSH formulation. [Figure 4](#f4){ref-type="fig"} displays the experimental results for the first-order correlation degree, Δ*I* = *I*~1~ − *I*~2~, as a function of the angle *ϕ*. [Figure 4(a) and (b)](#f4){ref-type="fig"} correspond to the case with *θ* = 0 for *E*~//~ and , respectively, whereas the corresponding results for *θ* = *π*/4 are plotted in [Fig. 4(c) and (d)](#f4){ref-type="fig"}. From [Fig. 4(a)](#f4){ref-type="fig"}, the maximum of the first-order correlation appears at *ϕ* = 0, which is in agreement with *θ* = 0. At the same time, the minimum of the first-order correlation is also found at an orthogonal direction as shown in [Fig. 4(b)](#f4){ref-type="fig"}, which validates realization of the teleportation process. Similarly, as *θ* = *π*/4, Bob has measured the maximum of the first-order correlation at *ϕ* = *π*/4 and the minimum also appears at its orthogonal direction ([Fig. 4(c) and (d)](#f4){ref-type="fig"}). In fact, the above design is suitable for any linear polarization state. The corresponding experiment to teleport a circular polarized initial state was also performed by using the above scheme, similar teleportation process has been realized (see [Supplementary](#s1){ref-type="supplementary-material"}). In the teleportation process, it is not necessary for Alice to know where Bob is, the initial polarization state can be unknown to anyone not only Alice. Furthermore, the transfer of information from Alice to Bob can happen over arbitrary distances. These properties for the teleportation in the presented scheme completely agree with those described by D. Bouwmeester et. al., which this work\' results focus on[@b2]. Discovery of other schemes for quantum teleportation by using classical optics warrants further study. Conclusions =========== We have demonstrated experimentally the non-local classical optical correlation from the Bell\'s measurement used in tests of quantum non-locality. Based on such a classical EPR correlation, a classical analogy has been implemented to the true meaning of quantum teleportation. The presented results indicate that some non-local phenomena in quantum machines can be realized in classical optical signal processing. Thus, this study opens a new way to obtain the quantum information process in the classical optical communication network. It not only provokes deep thought on some basic physical problems such as essence of entanglement and correlation, but also shows potential application in classical and quantum information processes. Methods ======= Measurement method for the first-order field correlation -------------------------------------------------------- In general, the polarization-entangled photon pairs can be produced from spontaneous down-conversion of the nonlinear crystal. In such a process, the photon states for and polarizations are generated with a certain probability at the same time, which the entangled properties can be measured by the coincidence counts. Based on the coherence of light field, we can construct the corresponding non-local classical EPR correlation states as described by Eq.(4), which the correlated properties can be shown by the first-order field correlation. Basically, the measure of the first-order field correlation can be realized by synchronous local measurements and doesn\'t require direct contact. However, in the experiment it is difficult to obtain the first-order field correlation by directly measuring fields. In addition, the synchronization is very hard to achieve. So, we take the following method, that is, take and for example and do the following Hadamard transformation:thenwhere Re{X} represents the real part of X. From the experimental setup in [Fig.1](#f1){ref-type="fig"}, we can find From complete incoherent condition and ,it is easy to find the following relation:ThenThat is, the first-order field correlation can be measured by the difference of light intensities and this method is also effective in other measurements of experiments. The above process can be realized by the beam splitter as shown in [Figure 5](#f5){ref-type="fig"}. In the experiment, the same polarization for the light beams is required. Realization of Bell-state measurement for classical optical entangled states ---------------------------------------------------------------------------- Bell-state measurement is a key part in the teleportation scheme. In our teleportation scheme, we perform the Bell-state measurement referring to three-photon scheme described in Ref. [@b2] as shown in [Figure 6](#f6){ref-type="fig"}. The marks *π*/2 and *π*/4 in [Figure 6](#f6){ref-type="fig"} represent the angle between the axis of HWP and the horizontal direction. The functions of two HWPs are to realize interchange between and polarizations, add a *π* phase for the component of polarization field. The Jones matrix for the BS is taken in the following form:Two HWPs are put at the output port of the difference. If the input ports are in four Bell-states, the results by the correlation measurement of the first-order field are given in the [table 1](#t1){ref-type="table"}. Taking the antisymmetric state as an example, in the following we give a demonstration on such a result. The antisymmetric Bell state isThe corresponding field isAfter passing through the BS, they becomeConsider the output of the difference, perform interchange between and polarizations and add a *π* phase for the component of polarization field by the HWPs, we haveFrom the complete incoherent condition and the correlation measurement of the first-order field for two components in Eq.(14), we have:Similarly, consider three symmetric states passing through the above optical element group, we find that all outputs are zero. Here the effect of polarization is considered in the correlation measurement of the first-order field. Author Contributions ==================== Theoretical method is presented by Y.S., the corresponding experiments are performed by X.S. Thus, Y.S. and X.S. contributed equally to this work. In doing the experiments, X.S. get the help of H.Q., X.Z. and Z.Y., the idea and physical analysis are given by X.Z. All authors reviewed the manuscript. Supplementary Material {#s1} ====================== ###### Supplementary Information Supplementary Information This work was supported by the National Natural Science Foundation of China (Grant No. 11274042 and 61421001). ![Experimental setup for CHSH-type Bell inequality violation by using two separable classical light sources.\ E~1~ and E~2~ are two laser beams with different wavelengths. and denote the horizontal and vertical polarization components. (P)BS, (polarizing) beam splitter; HWP, half-wave plate. The first-order correlation measurement is performed between *E~ai~* and *E~bj~* (*i*, *j* = *h*, *v*).](srep09175-f1){#f1} ![The correlation functions *C*(*θ~a~*,*θ~b~*) as a function of polarization rotated angle *θ~a~* at *θ~b~* = 0° (a) and *θ~b~* = 45° (b).\ The circle dots and solid lines represent the experimental and theoretical results, respectively. The dashed lines mark the values of *θ~a~* to achieve the maximum violations of Bell inequalities.](srep09175-f2){#f2} ![Teleportation scheme showing principles and experimental set-up for the linear polarization case.\ The classical EPR source shown in the bottom plate is the same to that in [Fig. 1](#f1){ref-type="fig"}. Alice and Bob share an ancillary classical entangled states marked by and . Alice performs a joint Bell-state measurement on and the initial state marked by . After Alice has sent the measured result *E~ac~* as classical information to Bob, Bob performs the correlation measurement of the first-order field by using and *E~ac~*. *E*~\|\|~ and represent the transmission and reflection parts as passes through a rotated PBS, Δ*I* is the difference of the light intensities at two export positions.](srep09175-f3){#f3} ![Experimental (circle dots) and theoretical (solid lines) results from the correlation measurement of the first-order field for the linear polarization case, which are described by the differences of light intensities Δ*I* as a function of the angle *ϕ*.\ (a) and (b) correspond to the results for *E*~\|\|~ and , respectively, as the polarization of the initial state *θ* = 0; (c) and (d) display the corresponding results as *θ* = *π*/4.](srep09175-f4){#f4} ![Schematic picture for the first-order field correlation.](srep09175-f5){#f5} ![Design scheme for Bell-state measurement.](srep09175-f6){#f6} ###### The results for Bell-state measurement Bell-state Classical field E~a~ Classical field E~b~ The first-order field correlation ------------ ---------------------- ---------------------- ----------------------------------- \|*φ*~+~) 0 \|*φ*~−~) 0 \|*ψ*~+~) 0 \|*ψ*~−~) 1 [^1]: These authors contributed equally to this work.

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But despite the craze, some said that the supermoon had appeared quite similar to other full moons in the past and was fairly "imperceptible," Universe Today reports. In fact, according to a report, the closest full moon in 2017 will only be 0.02 percent farther away than November's supermoon. What is a supermoon? A supermoon occurs when the moon is at its closest point of approach in its orbit around the world. According to NASA, the term supermoon became popular in recent years, referring to a new or full moon that is within 90 percent of its closest approach to the planet, which makes it appear 14 percent bigger and 30 percent brighter in the sky. Since the moon's orbit is elliptical, one side (perigee) is about 30,000 mils closer to Earth than the other (apogee). When the Earth, sun and the moon line up as the moon orbits the Earth (syzygy), and the moon is on the opposite side of the Earth from the sun (perigee-syzygy), a perigee moon or supermoon occurs. The Nov. 14 full moon will be the closest since 1948, and the next time the full moon will come this close again will be on Nov. 25, 2034. The November supermoon is also called Beaver Moon, as it arrives at the time of year when hunters are said to be setting traps on the swamps before they froze over to make sure they will have enough furs to cover up for the winter. Where to see it Stargazers could catch the supermoon on Nov. 14 at 8:52 a.m. EST. To get a better view of the moon, it is recommended to go to the top floor of a building during dusk, facing east.

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In recent years, movements of construction of a wireless communication network using a flying object such as a satellite and a balloon have been active. The wireless communication network using a flying object has an advantage that, in comparison with a communication network constructed on a surface of the ground, a base station is unlikely to encounter a disaster, for example, by constructing the base station on a flying object, and thereby disaster-resistant property is improved. Further, the wireless communication network using a flying object also has an advantage that a cost for construction such as installation of wiring facilities can be reduced. It is predicted that users of such a wireless communication network using a flying object increase, and with an increase of the users, it is supposed that frequency bands of radio waves used in the wireless communication network are tight. Therefore, as wireless communication used in the wireless communication network using a flying object, attention is paid to free space optics (FSO) using an optical frequency band expected to become markedly broadband, instead of microwaves that are currently mainstream. In order to achieve a large-capacity free space optics system, a speeding-up technique of a bit rate of a transmission signal light and a wavelength division multiplexing technique are required. Further, in a free space optics system, since a signal light is propagated for a long distance between a flying object in midair and the ground, attenuation of the signal light during the propagation is large, and therefore a high-sensitive reception device is required. For the reception device, a technique common to an optical fiber communication technique, specifically, an optical transmission/reception technique using a single mode fiber (SMF) is applied. The reason why the single mode fiber is used in a free space optics system is that an optical transmission/reception technique such as a low-noise and high-gain direct optical amplification technique, a high-sensitive digital coherent reception technique, a high bit-rate transmission/reception technique, and a dense wavelength division multiplexing (DWDM) technique can be used. In a free space optics system using a single mode fiber, it is necessary for a signal light (laser light) propagated in a free space to enter (be coupled with) a core having a small core diameter in the single mode fiber. Therefore, in a free space optics system between a flying object in midair such as an artificial satellite, and a ground station, in order to condense sufficient optical power, a reception device needs to include a telescope having a large aperture diameter. Herein, an aperture of the telescope is equal to or more than several times a spatial coherence radius of a signal light (laser light) propagated in the atmosphere, and therefore the signal light is likely to be affected by turbulence of the atmosphere such as wind. In other words, when passing through a portion where a local fluctuation of a refractive index of the atmosphere caused by a turbulence phenomenon and a thermal phenomenon occurs, a signal light is refracted and the signal light is deflected due to the refraction. Therefore, a disturbance of a beam spot of a signal light condensed by a telescope increases. In this manner, an intensity of a signal light that enters a reception device largely varies due to a disturbance of a beam spot, and therefore, in a free space optics system, a problem that stable communication is difficult occurs. In particular, when a large attenuation (fade) of a signal light due to a large intensity variation occurs, an error or lack of reception data is caused. Therefore, in a free space optics system, a problem that an overhead of forward error correction (FEC) increases and a problem that retransmission processing becomes necessary occur. Such problems cause a decrease in an effective throughput of a free space optics system. As described above, in a free space optics system, due to a disturbance of a wave-front to which a signal light is subjected during atmospheric propagation, a problem that communication becomes unstable may occur. A large number of techniques for solving such the problem have been proposed heretofore. A reception device disclosed in PTL 1 (Japanese Translation of PCT International Application Publication No. 2013-535871) includes a light condensing unit, a wavelength demultiplexer, a plurality of optical detectors, and a signal processing unit. The reception device is configured to collect light on a plurality of individual fiber end faces from the wavelength demultiplexer and converge a signal light to a single output fiber to be input to the optical detector by using a fiber bundle or the like that is gradually thinner. By such a configuration, in the reception device, stable fiber coupling is achieved even against a disturbance of a beam spot. Further, PTL 1 also discloses a configuration in which a core diameter is decreased to a diameter equal to that of a single mode fiber in a tapered shape, and thereby a coupled signal light is converged on a core of the single mode fiber and connection to an optical component adapted to a next-stage single mode fiber is made possible. A communication device that constructs a free space optics system disclosed in PTL 2 (Japanese Registered Patent Publication No. 4701454) includes a light condensing unit, a fiber bundle, a plurality of optical receivers, a plurality of optical transmitters, and a transmission/reception control unit. The communication device is configured to transmit a signal light from the same position as a light condensing position of a signal light received from an opposite device. By this configuration, regardless of deflection of a light condensing system due to an atmospheric fluctuation and a peripheral temperature change, in the opposite device side, a signal light from the communication device is condensed to a signal light emission point. NPL 1 (“Next-generation Extremely Large Optical Infrared Telescope Planning Instructions”) discloses an adaptive optics (AO) technique that measures and corrects distortion of a wave-front of a signal light. In the technique, a wave-front of a reception light distorted due to an atmospheric fluctuation is observed by a wave-front sensor and a wave-front correction element using a micro electro mechanical system (MEMS) or the like is controlled by using the observation result.

3.53125

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The drive system for a rotating apparatus (such as a centrifuge instrument) typically includes a shaft attached at one end to a motive force (e. g., an electric motor). The shaft supports a load somewhere along its length. One inherent property of such a drive system is load imbalance. Even a very small imbalance in the otherwise symmetrical mass distribution about the drive shaft can cause damaging vibrations. The magnitude of the imbalance places a load on the bearings. This problem can be addressed by providing a degree of flexibility to the drive shaft. However, as this rotating apparatus accelerates to its operating speed the system passes through several critical speeds. A thin, elongate shaft rotating about its longitudinal axis possesses certain natural frequencies of vibration that become apparent at these critical speeds. Passage through a critical speed thus causes the drive system to vibrate, which in turn magnifies the load imposed on the bearings. This increase in load can significantly reduce the life of the bearing. In the example of a centrifuge instrument the vibration may also have a detrimental effect on the sample that is being processed within the rotor of the instrument. Several methods have been proposed in the art to solve the problem of vibration generated during passage of a drive system of a rotating apparatus through a critical rotational speed. One solution is to attempt to damp the vibrations imposed on the system. U.S. Pat. No. 5,026,341 (Giebeler) is an example of a rotating system for use in a centrifuge instrument that restricts the deflection of the shaft, thus damping vibration. Another solution, exemplified by the arrangement disclosed in U.S. Pat. No. 4,236,426 (Meinke et al.), is to alter the physical properties of the drive system in a speed-dependent fashion. As a result, for a first portion of the speed regime of the apparatus, the stiffness of the system is such that the critical speed lies well beyond a predetermined speed threshold. However, once the speed threshold is crossed the stiffness of the system is dynamically altered such that the critical speed of the modified drive lies at a speed that is well below the predetermined threshold. Thus, as the apparatus accelerates through its fill speed regime to its operating speed the critical speeds associated with both the original and the modified drives are avoided. In an arrangement as shown in the Meinke et al. patent, springs, dampers and/or masses are actively coupled and uncoupled in response to the changes in the deflection of the shaft. This coupling and uncoupling has the effect of altering the critical rotational speeds. Implementation of either of the above-described expedients usually requires a complex mechanism to effect the interaction between rotating and non-rotating parts of the drive system. In either case, technical difficulties can result. Therefore, in view of the foregoing it is believed advantageous to provide an arrangement of the type which dynamically alters the stiffness of the drive system, yet which does so without undue mechanical complexity.

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Pediatric migraine: recognition and treatment. The diagnosis of migraine headache in childhood rests on criteria similar to those used in migraine in adults. It is important, however, to appreciate several fundamental differences. These differences include the duration of attack, which is often far shorter than in an adult, and the location of the attack, which may be bilateral in many children. The treatment of children and adolescents with migraines includes treatment modalities for acute attacks, preventive medications when the attacks are frequent, and biobehavioral modes of therapy to address long-term management of the disorder. The controlled clinical trials of medications in pediatric migraine have suffered from high placebo response rates that may be related to the sites conducting the study (ie, headache specialist vs clinical research organizations). The medications have proved to be safe in the pediatric age group. Treatment modalities for acute migraine include over-the-counter nonsteroidal anti-inflammatory drugs (NSAIDs), as well as the oral triptans such as sumatriptan succinate, rizatriptan benzoate, and zolmitriptan and the nasal spray formulations of sumatriptan and zolmitriptan. Subcutaneous sumatriptan and parenteral dihydroergotamine have also been used limitedly. Preventive treatment for patients with frequent or disabling migraines (or both) includes the antidepressants amitriptyline hydrochloride and nortriptyline hydrochloride, the anticonvulsants divalproex sodium and topiramate, and the antihistaminic agent cyprohepatine hydrochloride. Biobehavioral approaches aimed at addressing the fundamental lifestyle issues and nonpharmacologic approaches to management are fundamental to long-term success.

3.578125

4

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Q: Darkest matter on Earth ("pure black") What is (for a human's eyes) the natural or synthetical matter on Earth (i.e. not in Space) that emits the least quantity of visible photons while being lightened by sunlight? In this matter, how is light converted? Invisible wavelengths (ultraviolet, X-rays)? Heat? A: "Vantablack, made out of carbon nanotubes, is designed by Surrey NanoSystems and absorbs 99.96% of all light that hits it. Conventional black, such as black paint or fabric, absorbs between 95% and 98% of light."

3.03125

3

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A scanning probe microscope (SPM) brings a pointed probe close to a sample to detect the interaction between the probe and the sample (a tunnel current, an interactive force, or the like). The scanning probe microscope then feedback-controls the distance between the probe and the sample so as to keep the interaction constant. Moreover, the SPM scans the probe (or the sample) in the horizontal direction with the feedback control maintained. Thus, the probe (or the sample) moves up and down so as to trace recesses and protrusions on the sample. An image of the recesses and protrusions on the surface of the sample can be obtained by recording the track of the feedback scanning with respect to the horizontal position. A known example of the SPM is an atomic force microscope (AFM). The AFM detects an interactive force acting between the probe and the sample. The AFM then feedback-controls the distance between the probe and the sample so as to keep the interactive force constant. The AFM uses a cantilever with a pointed probe provided at the tip thereof, as a force detector. When the probe is brought closer to the sample, the cantilever is displaced by the interactive force acting between the probe and the sample. This type of AFM configured to detect the interactive force based on the amount of displacement is called a contact mode AFM or a static mode AFM. On the other hand, a type of AFM configured to mechanically excite the cantilever at a frequency close to the resonant frequency thereof is called a dynamic AFM. The dynamic AFM detects the interactive force acting between the probe and the sample, based on a variation in vibration amplitude, frequency, phase caused by the interactive force. AFMs detecting the interactive force using the amplitude, frequency, and phase are called an AM-AFM, an FM-AFM, and a PM-AFM, respectively. The conventional dynamic mode AFM is disclosed in, for example, Japanese Patent Laid-Open No. 2004-226237. This document discloses an example of the FM-AFM. FIG. 1 shows a general configuration of a dynamic mode AFM. An AFM 101 includes a cantilever 103, a sample stage 105, a scanner 107, and an excitation unit 109. The scanner 107 is, for example, a piezo actuator and moves a sample on the sample stage 105 in an X direction, a Y direction, and a Z direction to scan a sample and the cantilever 103 relative to each other. The excitation unit 109 is also, for example, a piezo actuator and excites the cantilever 103. For example, an amplifier configured to drive an actuator is omitted from FIG. 1. An excitation and detection circuit 111 is configured to provide an excitation control function and a function to detect an interactive force. The excitation and detection circuit 111 applies an excitation signal to the excitation unit 109 to excite the cantilever 103. Furthermore, the excitation and detection circuit 111 detects, as the amount of the interaction between the probe and the sample, the amplitude, frequency, or phase of a displacement signal from the cantilever 103 detected by the sensor 113. The detected value is output to a feedback circuit 115 as a feedback signal and used to control the vertical position of the scanner 107. As a result, a feedback loop is formed which keeps the distance between the probe and the sample constant. As described above, in the present specification, a circuit functioning as an excitation control circuit and an interaction detection circuit is referred to as the “excitation and detection circuit”. Several types of methods are available for implementing the excitation and detection circuit. The excitation and detection circuit can be roughly classified into an analog type and a digital type. The digital type is now mainly used because the specifications of the digital type can be flexibly changed and because the digital type can implement complicated signal processing. FIG. 2 shows an example of an implemented excitation and detection circuit of a conventional digital type. The configuration in FIG. 2 corresponds to the AM-AFM and the PM-AFM and generates an excitation signal and detects an amplitude signal and a phase difference signal. The amplitude signal indicates the vibration amplitude of the cantilever. The phase difference signal indicates the difference in phase between the excitation signal for the cantilever and a displacement signal from the cantilever. As shown in FIG. 2, an excitation and detection circuit 121 includes a DDS (Direct Digital Synthesizer) 123 and a lock-in amplifier 125. The DDS 123 corresponds to an excitation control circuit. The lock-in amplifier 125 corresponds to a detection circuit for the amplitude and phase difference. In FIG. 2, the DDS 123 generates an excitation signal cos(2πft) that varies at an excitation frequency f. The DDS 123 holds sine-wave output values with respect to the phase, in the form of a lookup table. A sine wave signal is obtained by interpolating discreet values in the lookup table. The signal is not only output as the excitation signal for the cantilever but is also utilized as a reference signal for the lock-in amplifier 125 formed of a digital circuit. The lock-in amplifier 125 is a two-phase digital lock-in amplifier. A displacement signal Acos(2πft+φ) from the cantilever is input to the lock-in amplifier 125. The excitation signal cos(2πft) is also input to the lock-in amplifier 125 as the reference signal as described above. The reference signal is input to a 90° phase shift circuit (for example, a Hilbert conversion circuit) and a delay circuit, which then convert the signal into sin(2πft) and cos(2πft), respectively. These signals are converted into X=Acos(φ) and Y=Asin(φ), respectively, through a multiplication circuit and an LPF (Low Pass Filter). The multiplication circuit multiples each of the signals by the input displacement signal Acos(2πft+φ). The LPF removes high frequency components from the signals. Then, a vector calculation circuit calculates the absolute value R and argument θ of a complex input X+jY. The absolute value R is (X2+Y2)1/2, and the argument θ is tan−1(Y/X). The absolute value R corresponds to the amplitude A of the displacement signal. The argument θ corresponds to the phase difference φ between the displacement signal and the excitation signal. Thus, R and θ are output as the amplitude signal A and the phase difference signal φ, respectively. The configuration in FIG. 2 corresponds to an AM-AFM mode and a PM-AFM mode. In the AM-AFM mode, the amplitude signal A is output as a feedback signal and used for feedback control. The feedback control is performed such that the amplitude signal A equals a target amplitude. In the PM-ADM mode, the phase difference signal φ is output as a feedback signal and used for feedback control. In this case, the feedback control is performed such that the phase difference signal φ equals a target phase difference. Now, the configuration of the excitation and detection circuit for the FM-AFM will be described with reference to FIG. 3 and FIG. 4. FIG. 3 is a diagram based on which the principle of the FM-AFM will be described, and illustrates the characteristics of amplitude and phase of the cantilever. In an upper graph in FIG. 3, the axis of abscissas indicates frequency, and the axis of ordinate indicates the amplitude of the cantilever. In a lower graph in FIG. 3, the axis of abscissas indicates the frequency, and the axis of ordinate indicates the difference in phase between the excitation signal for the cantilever and displacement signal from the cantilever. As shown by a dotted line in the upper graph in FIG. 3, the resonant frequency f of the cantilever varies (shifts) as a result of the interaction between the cantilever and the sample. In FIG. 3, the amount of variation in resonant frequency is indicated by Δf. Furthermore, as shown in the lower graph, when the cantilever vibrates at the resonant frequency, the phase difference φ between the excitation signal and the displacement signal is 90°. Thus, the FM-AFM sets a target value for the phase difference φ to 90°, and controls the excitation signal such that the phase difference φ equals the target value. This excitation control is achieved by a phase locked loop (PLL) circuit and is such that even if the resonant frequency of the cantilever is varied by the interaction, the cantilever continues to vibrate at the resonant frequency. During this control, a variation in resonant frequency Δf is detected. Then, the feedback control is performed so as to keep the variation in resonant frequency Δf constant. FIG. 4 shows an example of an implemented excitation and detection circuit corresponding to the FM-AFM. The excitation and detection circuit generates an excitation signal and detects a frequency signal. The frequency signal is indicative of a variation in the resonant frequency of the cantilever caused by the interaction between the cantilever and the sample as described above. As shown in FIG. 4, an FM-AFM excitation and detection circuit 131 includes a proportional integral (PI) control circuit 137 in addition to a DDS 133 and a lock-in amplifier 135 (two-phase digital lock-in amplifier). An excitation signal cos(2πft) output by the DDS 133 is input to the lock-in amplifier 135 as a reference signal. Furthermore, a displacement signal Acos(2πft+φ) from the cantilever is input to the lock-in amplifier 135. The lock-in amplifier 135 has a configuration similar to that of the lock-in amplifier 125 in FIG. 2 to output the phase difference φ between the excitation signal and the displacement signal. Here, the lock-in amplifier 135 functions as a multiplying phase comparator to perform phase comparison based on multiplication of the displacement signal. A phase difference φ generated by the lock-in amplifier 135 is input to a PI control circuit 137. The PI control circuit 137 controls an output 2πΔfT (reference character T denotes a sampling period for input and output signals) such that the input phase difference φ equals a target value φ0. The output 2πΔfT is input to the DDS 133 to vary the frequency f of an output signal (excitation signal) cos(2πft) of the DDS 133. The frequency f varies around the free-running frequency f0 (an oscillation frequency obtained when the input is 0) of the DDS by Δf. In the configuration in FIG. 4, the DDS 133, the lock-in amplifier 135, and the PI control circuit 137 form the phase locked loop (PLL) circuit. The PI control circuit 137 functions as a loop filter for the PLL circuit. The PLL circuit varies the value of the frequency f of the excitation signal so that the frequency of the displacement signal equals that of the excitation signal, that is, f=f0+Δf. Thus, an output value from the PI control circuit 137 is proportional to a variation in the frequency of the displacement signal. Thus, the output value from the PI control circuit 137 is output as the frequency signal. Furthermore, the difference in phase between the displacement signal and the excitation signal can be adjusted by varying the target value φ0 for the PI control circuit 137. As described with reference to FIG. 3, the FM-AFM sets the target phase difference to 90°. Thus, the phase difference φ is kept at 90°, and the cantilever vibrates at the resonant frequency. Even if the resonant frequency of the cantilever is varied by the interaction between the cantilever and the sample, the cantilever continues to vibrate at the resonant frequency. The frequency signal has a value indicative of a variation (shift) Δf in the resonant frequency of the cantilever. The frequency signal is used for feedback control. The conventional AFM excitation and detection circuit has been described. There is still room to improve of the conventional circuit configuration as described below. In the conventional technique illustrated in FIG. 2, the lock-in amplifier functions as a multiplying phase comparator and internally compares the excitation signal with the displacement signal by multiplication. This leads to generation of an unwanted harmonic component. More specifically, an output from the multiplication circuit in the lock-in amplifier contains a component of the difference in frequency between input signals and a component of the sum of the frequencies of the input signals. The sum component corresponds to the unwanted harmonic component. The harmonic component cannot completely be removed even by the LPF arranged after the lock-in amplifier. Such a residual harmonic component may not only distort an output waveform but also affect the feedback control as described below. The AFM forms a feedback loop for control of the probe-sample distance, and the excitation and detection circuit is present in the feedback loop as shown in FIG. 1. A signal in which the harmonic component is mixed in the lock-in amplifier is used in the feedback loop. In this case, a feedback gain needs to be limited to a small value in order to avoid oscillation at the frequency of the harmonic component. This conventionally constitutes a factor preventing quick and stable feedback control from being achieved. In the FM-AFM circuit configuration shown in FIG. 4, as is the case with the circuit in FIG. 2, the lock-in amplifier functions as a multiplying phase comparator, leading to generation of an unwanted harmonic component. In particular, in the FM-AFM, the harmonic component not only limits the feedback gain but also works against the PLL circuit. This will be described below. In the FM-AFM configuration shown in FIG. 4, the lock-in amplifier is a part of the PLL circuit. Thus, the lock-in amplifier (multiplying phase comparator) generates an unwanted harmonic component in the loop in the PLL circuit. The harmonic component cannot completely be removed even by the LPF arranged after the lock-in amplifier. In particular, the LPF is present in the loop in the PLL and is thus subject to another restriction; the LPF cannot be designed independently of the response characteristics of the PLL. Thus, removal of the harmonic component in the FM-AFM is more difficult than in the AM-AFM and the PM-AFM. Because of the residual harmonic component, an increase in the gain of the PLL causes the PLL circuit to oscillate at the frequency of the residual harmonic component. Thus, in the conventional technique, the gain of the PLL is limited, preventing the frequency from being detected quickly and stably. As described above, in the FM-AFM, disadvantageously, the harmonic component limits not only the feedback gain of the whole AFM but also the gain of the PLL.

3.203125

3

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Although the Universe may seem spacious most galaxies are clumped together in groups or clusters and a neighbour is never far away. But this galaxy, known as NGC 6503, has found itself in a lonely position, shown here at ... European aircraft and aerospace giant Airbus has unveiled plans for a reusable space rocket launcher that should be ready in 2025, which the firm says will be radically different from the concept of rival US firm Space X. Skygazers at northern latitudes are familiar with the W-shaped star pattern of Cassiopeia the Queen. This circumpolar constellation is visible year-round near the North Star. Tucked next to one leg of the W lies a modest ... Space Space is the boundless, three-dimensional extent in which objects and events occur and have relative position and direction. Physical space is often conceived in three linear dimensions, although modern physicists usually consider it, with time, to be part of the boundless four-dimensional continuum known as spacetime. In mathematics spaces with different numbers of dimensions and with different underlying structures can be examined. The concept of space is considered to be of fundamental importance to an understanding of the universe although disagreement continues between philosophers over whether it is itself an entity, a relationship between entities, or part of a conceptual framework. Many of the philosophical questions arose in the 17th century, during the early development of classical mechanics. In Isaac Newton's view, space was absolute - in the sense that it existed permanently and independently of whether there were any matter in the space. Other natural philosophers, notably Gottfried Leibniz, thought instead that space was a collection of relations between objects, given by their distance and direction from one another. In the 18th century, Immanuel Kant described space and time as elements of a systematic framework which humans use to structure their experience. In the 19th and 20th centuries mathematicians began to examine non-Euclidean geometries, in which space can be said to be curved, rather than flat. According to Albert Einstein's theory of general relativity, space around gravitational fields deviates from Euclidean space. Experimental tests of general relativity have confirmed that non-Euclidean space provides a better model for explaining the existing laws of mechanics and optics.

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In a find that sheds light on how Earth-like planets may form, astronomers have reported finding the first evidence of small, sandy particles orbiting a newborn solar system at about the same distance as the Earth orbits the sun. "Precisely how and when planets form is an open question," said study co-author Christopher Johns-Krull, assistant professor of physics and astronomy at Rice University. "We believe the disk-shaped clouds of dust around newly formed stars condense, forming microscopic grains of sand that eventually go on to become pebbles, boulders and whole planets." In previous studies, astronomers have used infrared heat signals to identify microscopic dust particles around distant stars, but the method isn't precise enough to tell astronomers just how big they become, and whether the particles orbit near the star, like the Earth does the sun, or much further away at a distance more akin to Jupiter or Saturn. In the new study, Johns-Krull and co-authors in the United States, Germany and Uzbekistan used reflected light from the sand itself to confirm the Earth-like orbit of grainy particles around a pair of stars called KH-15D in the constellation Monoceros. The stars are about 2,400 light years from Earth in the Cone Nebula, and they are only about 3 million years old, compared to the sun's 4.5 billion years. "We were attracted to this system because it appears bright and dim at different times, which is odd," Johns-Krull said. The researchers found that the Earth has a nearly edge-on view of KH-15D. From this perspective, the disk blocks one of the stars from view, but its twin has an eccentric orbit that causes it to rise above the disk at regular intervals. "These eclipses let us study the system with the star there and with the star effectively not there," Johns-Krull said. "It's a very fortuitous arrangement because when the star is there all the time, it's so bright that we can't see the sand." The team conducted both photometric and spectrographic analyses of data collected during the past 12 years from a dozen observatories, including the McDonald Observatory in west Texas, the Keck Observatory in Hawaii and the VLT on Mount Paranal in Chile. "Because of how the light is being reflected there are opportunities to make observations about the chemical composition of these sand-like particles," said co-author William Herbst, an astronomer at Wesleyan University in Middletown, Conn. "That's very exciting because it opens up so many doors for new type of research on this disk." The report is to be published online by the journal Nature. Co-authors include Catrina Hamilton of Dickinson College; Katherine LeDuc of Wesleyan University; Joshua Winn of the Massachusetts Institute of Technology; Reinhard Mundt of the Max Planck Institute for Astronomy in Heidelberg, Germany; and Mansur Ibrahimov of the Ulugh Beg Astronomical Institute in Tashkent, Uzbekistan.The research was funded by NASA and the Keck Foundation.

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Structure Use parentheses when instantiating classes regardless of the number of arguments the constructor has. Declare class properties before methods. Declare public methods first, then protected ones and finally private ones. The exceptions (when using PHPUnit) to this rule are the class constructor and the setUp and tearDown methods of PHPUnit tests, which should always be the first methods to increase readability. Traits Traits are treated as classes. Ternary Operator Ternary operators are permissible when the entire ternary operation fits on one line. Longer ternaries should be split into if else statements. Ternary operators should not ever be nested. Optionally parentheses can be used around the condition check of the ternary for clarity: Most IDEs even nowadays can't show start/end for keywords, with brackets it always works in pretty much every IDE, though. If you intend to use the keywords in template files, you should at least be consistent and use them througout the files. But in general it is better to also stick to curly brackets here for consistency throughout the codebase. PHP Open Tags Always use <?php or <?= instead of <?. The <?= form should be used for echoing values of simple variables while the <?php form can be used for more complex code. The short form is supported by the newest PHP versions as well and it makes your files less verbose, thus easier to read. It doesn't even require the semicolon (;) so feel free to omit it. This <?= $x ?> way. If you want to comment it out then you can do it easily: This <?//= $x ?> way. Commenting out with  should be avoided as it is then visible in the resulting HTML output. Comparison Always try to be as strict as possible. If a non-strict test is deliberate it might be wise to comment it as such to avoid confusing it for a mistake. For testing if a variable is null, it is recommended to use a strict check: Multi-line declaration/condition/concatenation Multi-line control structures should have the parentheses in their own lines (similar to classes and methods): if ( ($a==$b)&& ($b==$c)|| (Foo::CONST==$d)) {$a=$d;} Careful with deep arrays One mistake that often gets made: $foo= [[0,1, 2], 3, 4]; This would effectively change all lines (and their indentation), if the array structure got normalized. Arrays also need to minimize effects on the resulting diff, and as such indentation must always be the right one: $foo= [[0,1, 2 ], 3, 4]; for example, max. normalized as: $foo= [ [0,1,2 ],3,4]; As you can see, entries like 0 would not need any change on reorganizing, thus reducing overhead in work and making diffs easier to read as they only show actual changes made. Typehinting Arguments that expect objects, arrays or callbacks (callable) can be typehinted. We only typehint public methods, though, as typehinting is not cost-free: Avoid no-op methods The first would allow no-ops like $this->foo() which does not do any operation at all. So semantically this makes no sense. In this case no default value may be used and a first argument is actually required for the first if statement to make sense ($this->foo($requiredArgument)). You can still pass null, of course, to break out early. Default values may only be used if their usage does make this method still do an operation (apart from returning early). Avoid private for class methods/properties Most of the time private is used too eagerly, where protected would suffice. Allow extending classes to extend the code. Don't assume it doesn't have to. This is especially important for frameworks or vendor libraries that people would like to enhance or customize in their applications. In case you are acquainted with the "Open/Close Principle", it is in some cases OK to use private to define clear public interfaces for classes. Underscores for Private/Protected It is not directly disallowed in PSR-2 to have the _ and __ visibility prefixes. But it says one has a good reason to use them. As most IDEs still don't really clearly display (in colors?) the difference between public, protected and private, the following would be difficult to read: Note that __ is also used for magic calls, and as such this recommendation is best used with the above hint of not using private visibility in your code. Otherwise please disregard and make sure you use an IDE that can display them properly. Using underscores with a lot of private methods will probably be worse than sticking to the PSR-2 recommendation. Return void vs null @return void shall be used to document when a method is expected not to return anything, and when there is just a return; as "early return". Explicitly returning with return null; or return $this->foo(); shall be documented be as @return null etc. HTML All tags and attributes are lowercase. CSS Definition ideally as dashed name: class: .some-class-name id: #some-id-to-an-element Both with lowercase characters (although classes are not case-sensitive, id's are!), the separator is minus [-]. You can use underscore [_] if it makes the separation of the identifier and the record id easier. E.g. my-id_33. It will become necessary to do so if you use UUIDs (which contain minus chars). Note: ids should be unique on the current page - so don't use them for iterating elements. In general all styling should be class based. Ids are often abused for that. But they usually serve the purpose of being identifiable via JS. So they should ideally be mainly used for dynamic JS scripts. Do not name the fields after their style, but after the function/meaning - as the style can change and will result in things like .red { color: yellow;}. JS Ideally, JS related classes are prefixed with js- to separate them from the rest of the CSS and styling related class names: <divclass="js-widget-toggle some-styling-class">...</div> Further considerations While so far the main focus was on the developer (readability), there are some additional optional guidelines that can help to further reduce diff size on code modification (maintainability). Those can and should be automated, though, as there is no point in forcing the developer to take care of those manually. The main idea is to keep each line independant from the others so removing or adding lines has minimal impact. Multi-line arrays Arrays that span across multiple lines can have a trailing comma to make sure that adding new rows does not change the previous row, as well. $array= ['first','second', // Note the trailing comma]; Multi-line logic For longer logic (method calls, operations) it can be helpful to put the trailing semicolon at the next line. Especially for fluid programming this will not show the previous row as modified. $Object->doFirst()->doSecond(); This would also be consistent to the symmetric bracket placing in general.

3.546875

4

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Many restaurants, and especially fast food restaurants, prepare food in advance so that they can meet the daily fluctuations in demand that occur around breakfast time, lunch time, or dinner time. Food prepared in advance must be stored safely until it is delivered to the consumer. For many food products this means keeping the food product above a certain minimum threshold temperature to prevent spoilage. For other food products, it means keeping the food frozen or chilled. Either way, the food products need to be heated and held at an elevated temperature before being served to consumers. Although many systems exist to warm or heat food, many of these suffer from a number of drawbacks. For example, infrared (IR) heat lamps not only heat the food, but they also heat the surrounding environment. This can result in increased air conditioning costs for the restaurant. This problem may be exacerbated when the food products are in metal foil packaging since the metal foil may have a tendency to reflect the IR radiation away from the food product and into the surrounding environment. Furthermore, IR lamps tend to become quite hot, which poses a burn risk to restaurant employees and/or customers. Although warm air convection systems do not have many of the problems associated with IR lamps, warm air convection systems often cause food products to dry out. Both IR and warm air convection systems tend to steadily consume power regardless of how many food products are currently being heated. It would be desirable to provide an improved system for warming food that is energy efficient, safe, and effective. In one embodiment described herein, an induction heating system is used to warm food. The food may be packaged in food packaging that includes a current conducting material. The food packaging may be capable of being inductively heated to a temperature sufficient to warm the food.

3.28125

3

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A conventional technique for coating a phosphor on an LED, as shown in FIG. 1, includes directly applying a polymer material 20 such as epoxy, etc., into which the phosphor is mixed, onto an LED 10, and then, curing the polymer material 20. The conventional method of coating a phosphor on an LED has a problem that the polymer material 20 including the phosphor cannot be easily patterned. Therefore, in the conventional phosphor coating method, the phosphor must be applied to the entire surface after completion of wire bonding. In this case, when the LED to which the phosphor is applied cannot have desired performance (for example, in color, uniformity of color, etc.), the LED, which is expensive due to the wire bonding, is wasted, and thus, the overall manufacturing cost increases. In addition, the conventional method of coating a phosphor on the LED 10 is not appropriate for mass production. More specifically, in the conventional phosphor coating method, since the polymer material 20 including the phosphor must be separately coated onto each LED, the coating is expensive. Further, the conventional method of coating a phosphor on the LED 10 has a problem in that the thickness of the polymer material 20 including the phosphor cannot be easily adjusted. When the thickness of the polymer material 20 including the phosphor increases, intensity of light having a frequency varied by the phosphor increases, and when the thickness of the polymer material 20 including the phosphor decreases, intensity of light having a frequency varied by the phosphor decreases. Therefore, since the thickness of the polymer material 20 including the phosphor is an important factor for determining colors finally obtained from the LED 10, the thickness must be precisely controlled. In particular, since the light is emitted from side surfaces of the LED 10 as well as an upper surface thereof, the thickness of the polymer material 20 including the phosphor disposed on the side surfaces of the LED 10 as well as the thickness of the polymer material 20 including the phosphor disposed on the upper surface of the LED 10 must be precisely controlled. Furthermore, since the polymer material 20 including the phosphor is applied onto the LED 10 to a non-uniform thickness in the conventional method of coating a phosphor on the LED 10, uniform colors cannot be obtained. For example, when a white light is obtained by mixing a blue light emitted from a blue LED 10 and a yellow light obtained by a yellow phosphor, the white light with yellow color is transmitted to an observer 1 of FIG. 1 since the thickness of the polymer material 20 including the phosphor is large, and the white light with blue color is transmitted to an observer 2 of FIG. 1 since the thickness of the polymer material 20 including the phosphor is small.

3.078125

3

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GRADES OR AGES: Grade 5. SUBJECT MATTER: Social studies; economic development of the United States and Canada. ORGANIZATION AND PHYSICAL APPEARANCE: The major portion of the guide, which develops the unit, is laid out in three columns, one each for topics, activities, and materials. Other sections are in list form. The guide is mimeographed and staple-bound with a paper cover. OBJECTIVES AND ACTIVITIES: General objectives for the unit are listed on the first page. Each group of activities in the second column is related to a topic in the first column. INSTRUCTIONAL MATERIALS: Each group of materials listed in the third column is related to one or more activities. In addition, three appendixes contain curriculum materials. STUDENT ASSESSMENT: A one-page section entitled"Evaluation" lists ideas students should understand and skills they should possess by the end of the unit. OPTIONS: The guide is prescriptive as to course content and timing. Activities and materials listed are optional. Also, a short section lists several supplemental activities. (RT)

3.453125

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Identification and differentiation between colored pencils. With pencils of any color, the first step certainly involves visual examination to distinguish between the color tints and to study the quality of the stroke itself. In many instances by this step alone, 2 pencils can be distinguished if they are the product of 2 different manufacturers. In other words, the most useful of all tests is the visual examination. In the case of red pencils, infrared luminescence reveals significant information and should be resorted to in those instances where two questioned strokes are extremely similar. Study under ultraviolet radiation may also help to establish similarities or differences which are not readily discernible by visual examination. However, reflected infrared examination and study with dichroic filters have no particular value when dealing with red pencil although chemical spot testing may be of some assistance. In the case of blue pencils, a number of brands absorbs infrared radiation to a different extent and some give off distinctive infrared luminescence, so that these 2 tests can assist in distinguishing between certain similar colors or tints. Also, study through dichroic filters has value. Thus, the combination of these 3 tests can be of some advantage, but in most instances, particularly with dark blues, examination under ultraviolet radiation is not particularly helpful. Chemical spot testing has some limited advantages but generally only in combination with all other tests. In the case of green pencils, the same pattern of testing may be used as with blues. Many of the greens absorb infrared rays and some have bright infrared luminescence. Ultraviolet radiation can cause certain greens to fluoresce in a distinctive way. Thus, with each color studied, differences can be revealed and similarities established. Colored pencils are a distinct group of writing instruments. Within any color classification, there is a variety of shades or tints. Although it is not psosible to determine the make of pencil used in any particular writing, it is possible under many circumstances to distinguish between the work of different makes and grades of red, blue and green pencils, as well as other colors which have not been covered by this paper. While visual examination will separate the many different makes, other tests are described which will further assist in grouping or separating colored writing strokes. For a number of reasons, and particularly because of manufacturing procedures of different companies, not every make of pencil is distinctive, but there has been found to be a definite variety within each color group, and many makes are distinguishable.

3.140625

3

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Toronto: In a bid to determine whether distant stars with planets orbiting them can harbour life, a global team of astronomers has discovered a new way to measure the pull of gravity at the surface of distant stars. Knowing the surface gravity of a star is essentially knowing how much you would weigh on that star. If stars had solid surfaces on which you could stand, then your weight would change from star to star. The new method allows scientists to measure surface gravity with an accuracy of about four percent, for stars too distant and too faint to apply current techniques. Since surface gravity depends on the star's mass and radius (just as your weight on Earth depends on its mass and radius), this technique will enable astronomers to better gauge the masses and sizes of distant stars. “If you don't know the star, you don't know the planet. The size of an exoplanet is measured relative to the size of its parent star,” said study co-author and professor Jaymie Matthews from University of British Columbia. If you find a planet around a star that you think is Sun-like but is actually a giant, you may have fooled yourself into thinking you've found a habitable Earth-sized world. “Our technique can tell you how big and bright is the star, and if a planet around it is the right size and temperature to have water oceans, and maybe life,” Matthews added. The new technique called the “autocorrelation function timescale technique” or timescale technique for short, uses subtle variations in the brightness of distant stars recorded by satellites like Canada's MOST and NASA's Kepler missions. Future space satellites will hunt for planets in the 'Goldilocks Zones' of their stars. Not too hot, not too cold, but just right for liquid water oceans and maybe life. Future exoplanet surveys will need the best possible information about the stars they search, if they're to correctly characterize any planets they find. “The timescale technique is a simple but powerful tool that can be applied to the data from these searches to help understand the nature of stars like our Sun and to help find other planets like our Earth,” explained lead author Thomas Kallinger from University of Vienna. It will play an exciting role in the study of planets beyond the Solar System, many so distant that even the basic properties of the stars they orbit can't be measured accurately. The new method is described in a study published in the journal Science Advances.

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The inventive concept relates generally to electronic data storage technologies. More particularly, the inventive concept relates to data storage devices and related methods of operation. The information age has produced an explosive increase in the demand for personal data storage. With this increasing demand, various types of personal data storage devices have proliferated. For example, hard disk drives (HDDs) have been widely used due to various attractive features such as high recording density, high speed of data transmission, fast data access time, and low cost. Unfortunately, an HDD can be damaged by even slight shock and vibration due to its use of a platter and complex mechanical parts. In recent years, solid-state disks or drives (SSDs) have been developed to replace HDDs. An SSD is a data storage device that uses a solid-state semiconductor memory as a main form of data storage. Unlike HDDs, SSDs do not include a platter and related mechanical parts. As a result, SSDs tend to have lower mechanical driving time and latency, and faster read/write times compared with HDDs. They also tend to have fewer errors due to latency and mechanical friction compared with HDDs, so their reliability in performing read/write operations tends to be better than that of HDDs. Moreover, SSDs generate relatively little heat and noise during operation, and they can withstand physical shock, which makes them increasingly more attractive than HDDs. Due to the increasing popularity of SSDs, researchers are currently devoting great efforts to improving numerous aspects of their performance, including read/write speed, storage capacity, power consumption, reliability, durability, and many others.

3.34375

3

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This invention relates to the identification and use of cis acting nucleic acid elements that bind to nucleic acid binding factors to regulate genetic activities of nucleic acids. All living creatures store information in nucleic acid molecules called DNA or RNA that encode structural and regulatory proteins. The collective behavior of nucleic acids and proteins constitutes and controls normal cell and organismal life cycles. Nucleic acids and proteins also act as causative agents in, or response factors to, pathological conditions. Transcription of DNA into RNA, translation of RNA into proteins and other genetic events such as nucleic acid synthesis, sorting, processing, repair and degradation, are regulated by a variety of specialized nucleic acid binding factors. Nucleic acid binding factors bind to specific sequences present on the nucleic acid molecules they regulate, called cis acting nucleic acid elements. These nucleic acid binding factors, bound to their specific cis acting nucleic acid elements, are able to interact with other cellular factors to modulate specific genetic events. The binding of a nucleic acid binding factor to a cis acting nucleic acid element, or its ability to interact with other factors that mediate genetic events, or both, can be regulated in response to signals transmitted into the cell from the cell exterior. As an example, regulatory proteins called xe2x80x9ctranscription factorsxe2x80x9d bind to cis acting nucleic acid elements on genomic DNA at sites known as xe2x80x9cpromotersxe2x80x9d and xe2x80x9cenhancersxe2x80x9d present at variable distances from the site of initiation of transcription of the genes they regulate. The enhancer sequences and adjacent nucleic acid sequences, together with their bound transcription factors, are able to bend to contact the transcriptional complex bound to the promoter. Such contact can either enhance or reduce expression of the regulated gene. The human genome, which stores the genetic information of a human cell as DNA, is estimated to contain about 100,000 genes. Each of these genes and the RNAs they encode is likely to have multiple cis acting nucleic acid elements that bind to corresponding nucleic acid binding factors to regulate gene expression. These cis acting nucleic acid elements, and the factors that bind them, are potential targets for therapeutic drugs that could be used to modulate gene expression. Determining which cis acting nucleic acid elements are bound under different conditions can also be used to characterize and monitor the genetic responses of a cell under normal, pathological or experimental conditions. Current methods of identifying cis acting nucleic acid elements have several disadvantages. Most of these methods require prior identification of either the nucleic acid that is regulated, or the corresponding regulatory nucleic acid binding factor, or both. For example, once a nucleic acid has been identified, adjacent sequences, which are predicted to contain cis acting nucleic acid elements, can be isolated and subsequences therefrom are tested for cis activities. Alternatively, once a nucleic acid binding factor has been isolated, the sequences to which it binds can be identified. Other methods, which are limited to identifying transcriptional enhancer elements, involve cloning random nucleic acid sequences upstream of a reporter gene and observing expression of the reporter gene product. At present, however, there is no broadly applicable method to identify cis acting nucleic acid elements without prior identification of the regulated nucleic acid or of the regulatory nucleic acid binding factor. There is also no rapid and efficient method to simultaneously identify a plurality of cis acting nucleic acid elements. Thus, there exists a need for a method of rapidly and efficiently identifying cis acting nucleic acid elements. The present invention satisfies this need and provides related advantages as well. The invention provides a method of identifying nucleic acids containing cis acting nucleic acid elements. The method consists of contacting a diverse population of nucleic acid binding factors with a diverse population of isolated nucleic acid molecules under conditions that allow the nucleic acid binding factors to selectively bind the nucleic acids. The nucleic acids that bind the nucleic acid binding factors are identified and are characterized as nucleic acids containing cis acting nucleic acid elements. The method simultaneously provides for the isolation of nucleic acid binding factors that selectively bind the isolated nucleic acid molecules. The invention also provides methods of identifying compounds that are cis acting nucleic acid element analogs, compounds that are nucleic acid binding factor analogs, and compounds that selectively bind cis acting nucleic acid elements. The invention further provides methods to identify compounds that selectively displace binding between a nucleic acid binding factor and a cis acting nucleic acid element or between nucleic acid binding factors. The invention further provides a plurality of isolated nucleic acid molecules that each contain one or more cis acting nucleic acid elements. Also provided is a plurality of isolated cis acting nucleic acid element analogs. The isolated nucleic acid molecules containing cis acting nucleic acid elements and the isolated cis acting nucleic acid element analogs in the pluralities can be bound to nucleic acid binding factors. A plurality of isolated nucleic acid binding factors is also provided. The invention also provides a method of determining a binding state of a nucleic acid. The method consists of contacting a nucleic acid with a plurality of isolated cis acting nucleic acid elements under conditions that allow nucleic acid binding factors bound to the nucleic acid to bind to the isolated cis acting nucleic acid elements. The isolated cis acting nucleic acid elements that bind the nucleic acid binding factors are identified and characterize the binding state of the nucleic acid. The invention further provides a method of treating a pathological condition in an individual. The method consists of administering to the individual an effective amount of a therapeutic agent that selectively alters the ability of a cis acting nucleic acid element to regulate a genetic activity of a nucleic acid involved in the pathological condition. Also provided is a method of treating a pathological condition in an individual by contacting a cell of the individual with an effective amount of a targeting construct that includes a cis acting nucleic acid element and targeting sequences. The targeting construct is taken up by the cell and inserted by homologous recombination into a nucleic acid involved in the pathological condition so as to alter a genetic activity of the nucleic acid.

3.046875

3

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Click on the image above to download a moderately sized image in JPEG format (possibly reduced in size from original) Original Caption Released with Image: Context image All this week, the THEMIS Image of the Day has been following on the real Mars the path taken by fictional astronaut Mark Watney, stranded on the Red Planet in the book and movie, The Martian. Generally smooth and rolling terrain covers most of this portion of Schiaparelli Crater's floor. Because the impact that made Schiaparelli occurred billions of years ago, nature has had ample time to leave lava and sediments in the crater and to erode them. The ridge in the image's southern end is part of an eroded crater rim, one of many such smaller impact craters that have collected on Schiaparelli's floor since it formed. (This image was taken as part of a study for the Mars Student Imaging Project by a high-school science class.) Here astronaut Mark Watney's great overland trek reaches its end. He arrives safely at the Mars Ascent Vehicle (MAV), which was sent in advance for the next Mars mission crew. The rocket will get him off the ground and into Mars orbit, where he can be picked up by a rescue ship coming from Earth. NASA's Jet Propulsion Laboratory manages the 2001 Mars Odyssey mission for NASA's Science Mission Directorate, Washington, D.C. The Thermal Emission Imaging System (THEMIS) was developed by Arizona State University, Tempe, in collaboration with Raytheon Santa Barbara Remote Sensing. The THEMIS investigation is led by Dr. Philip Christensen at Arizona State University. Lockheed Martin Astronautics, Denver, is the prime contractor for the Odyssey project, and developed and built the orbiter. Mission operations are conducted jointly from Lockheed Martin and from JPL, a division of the California Institute of Technology in Pasadena.

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Q: How to deform a 2d shape to make a 3d object? I have a 2d flat mesh that i would like to manipulate without any distortion to create a 3D shape. Typically for the pie below, joining the 2 edges together would make a 3D cone. Do you have any idea of which modifier to use ? A: Using a script to make the two shape keys. Change the r and h of result cone. Example of radius 1, height 2, 1 and 0.5 cones. import bpy import bmesh from mathutils import Vector from math import radians, sin, cos, sqrt from bpy import context # for testing r = 1 # radius of cone h = 1 # height of cone sectors = 16 l = sqrt(r**2 + h**2) # hypotenuse # sector will have angle theta = radians(360) * r / l dtheta = theta / sectors # build the base bm = bmesh.new() verts = [] for i in range(sectors + 1): a = i * dtheta verts.append(bm.verts.new((l * cos(a), l * sin(a), 0))) topvert = bm.verts.new((0, 0, 0)) for i in range(sectors): bm.faces.new([verts[i + 1], topvert, verts[i]]) cone_mesh = bpy.data.meshes.new("Cone") cone = bpy.data.objects.new("Cone", cone_mesh) bm.to_mesh(cone_mesh) # add base as basis shape key basis_shape_key = cone.shape_key_add("Basis") # add second shape key cone_shape_key = cone.shape_key_add("Cone") offset = (radians(360) - theta) / 2 dtheta = radians(360) / sectors for v in verts: a = v.index * dtheta - offset cone_shape_key.data[v.index].co = ((r * cos(a), r * sin(a), 0)) cone_shape_key.data[topvert.index].co = (0, 0, h) # link to scene scene = context.scene scene.objects.link(cone) scene.objects.active = cone cone.select = True A: Managed to approximate this with Shape Keys, starting out with a cone, it's easier than starting out with a flat shape and bending it into your will. Add a cone mesh with whatever final dimensions you want it to have Move it in edit mode so it's center is on the center of the base (not mid height) Erase the left part and the bottom face and then add a Mirror modifier Add two new shape keys one is the base as it currently is, and another (Key 1) will be it's flat shape. Now some math, in edit mode check the length of one of the cone large side edges with the 3D view > Properties Region > Mesh Display > Length that will determine the radius of the final flat shape Add a new mesh circle object, it's radius should be the length of the previously measured edge, and it the number radius vertices should be 1 1/4 the number of vertices of the cone. So if by default a cone has 32 vertex so the circle should have 1.25 x 32 = 40 vertices. Erase one quarter of the circle's edges so that they are centered around the edge you ripped in Step 3 Now with shape Key 1 selected enter edit mode on the cone, move the central vertex down until it is flat Scale all the vertex in the cone base so that they reach the circle radius (use snap for better precision) Press .(Period Key) to transform centered in 3D Cursor Hide all the cone vertex but the outer rim of the base, including the vertex at X=0 With Proportional Edit set to Connected and the Fallof type set to Linear, select only the lower vertex and rotate them all 1/8 of a turn, so they snap to the open end of the circle. Adjust the Proportional Edit radius with the mouse wheel. 13.Profit! (Adjust progression with the shapekey Value Slider) You may then give it a more natural or organic looking transition with some modifiers or with manually bending the shape a little with more shapekeys

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Pelican Island National Wildlife Refuge Pelican Island National Wildlife Refuge is a United States National Wildlife Refuge (NWR), and part of the Everglades Headwaters NWR complex, located just off the western coast of Orchid Island in the Indian River Lagoon east of Sebastian, Florida. The refuge consists of a island that includes an additional of surrounding water and is located off the east coast of Florida of the Indian River Lagoon. Established by an executive order of President Theodore Roosevelt on March 14, 1903, Pelican Island was the first National wildlife refuge in the United States. It was created to protect egrets and other birds from extinction through plume hunting. Management Pelican Island is administered as part of the Everglades Headwaters NWR complex along with Archie Carr NWR, Lake Wales Ridge NWR, and the Everglades Headwaters NWR and Conservation Area, created in 2012 (556th unit of the National Wildlife Refuge System) with a donation and other lands covering approximately north of Lake Okeechobee. will be held under "conservation easement"s through the U.S. Department of the Interior and the U.S. Fish and Wildlife Service. This allows landowners the right to retain ownership of the land, with the ability to continue farming or ranching, ensuring that the land can't be subdivided or developed. Pelican Island NWR has been placed on the List of Ramsar wetlands of international importance along with other areas of wetlands in the United States. Early history Pelican Island's bird populations were threatened because of increased American settlement around the area in the mid-19th century. Many of the exotic birds were killed for their feathers, used in the fashion industry. Plumes from the birds were used to adorn ladies' hats of the day and at the time were worth more than their weight in gold. Paul Kroegel, a German immigrant, moved to Florida in 1881 and lived on the west bank of Indian River Lagoon. He was fascinated with the pelicans on the island. Being able to see the island from his home, Paul would watch the pelicans and other water birds. He eventually took an interest in the island and its protection. However, there was not any state or federal law to help him so he took control of the situation himself. Kroegel sailed to the island to stand guard and protect the birds and the island. A few naturalists visited Kroegel at Pelican Island. A curator at the American Museum of Natural History in New York, Frank Chapman, was one of the naturalists showing interest in the island as well. He discovered that Pelican Island was one of the last rookeries of Brown pelicans on the eastern coast of Florida. The American Ornithologists' Union and the Florida Audubon Society led a campaign to pass legislation for protection of non-game birds in 1901. Knowing that the protection of Pelican Island would require more legislation, Chapman and his fellow advocate, William Dutcher went to President Theodore Roosevelt at his home in New York. The two appealed their case to Roosevelt's conservative ethics. President Roosevelt signed an executive order that established Pelican Island as the first federal bird reservation. This was the first time that the federal government put land aside for the sake of wildlife. The area, however, was open for big game hunters. Recent threats During the 1960s, Pelican Island was threatened by attempts to sell the surrounding wetlands and islands to developers. Local citizens led a fight to protect Pelican Island by stopping the sale of the wetlands. The Indian River Area Preservation League, formed by local citrus growers, commercial fishermen, and sportsmen, joined with Florida Audubon Society to convince the State to include the islands as a part of the refuge. "Later in 1963, Pelican Island was designated as a National Historic Landmark by the Secretary of the Interior because of its status as the first federal area set aside specifically to protect wildlife." In 1968, Florida agreed to expand to include nearly 5000 acres (20 km²) of mangrove islands and other submerged lands. And then in 1970, Pelican Island became the smallest wilderness area in the National Wilderness Preservation System. Since, the refuge has gained over 500 acres (2 km²) through purchases, management agreements, and conservation easements to provide a buffer against encroaching development and also to be a link to the Archie Carr National Wildlife Refuge. Pelican Island National Wildlife Refuge was added to the list of wetlands of international importance under the Ramsar Convention signed in 1971. Today, Pelican Island is also threatened by shoreline development. Shoreline development has many negative impacts associated with it. Shoreline development can reduce the water quality by increasing the runoff of sediments, fertilizers, and pesticides. These runoffs will cause decline in water quality, and this can directly affect the food base that sustains the island's nesting bird colonies. Waterfront development will also lead to more boat traffic. This extra boat traffic will also negatively affect the birds on the coast. Not only this, development of the shorelines of Pelican Island will permanently flaw the pristine character of this unique National Historic Landmark. Physical environment The environment of Pelican Island consists of climate, topography, geology, air quality, and waterways. Climate The climate at Pelican Island NWR is subtropical and temperate and experiences an average temperate of . Pelican Island has long, warm, and humid summers and short, mild winters and has an average rainfall of about annually. Pelican Island may experience tropical storms in the period from May to November. Topography The elevation of Pelican Island changes from east to west. It rises sharply from sea level to about and then drops back down more slowly to below sea level in the Indian River Lagoon. The land between the Indian River Lagoon and St. Sebastian River is . Even further west, there is an ancient dune that rises in elevation from to . Geology The landscape of Pelican Island area is made of Pleistocene (glacial) and Holocene (recent) origin. Submerged lands were exposed during the late Pleistocene period, allowing for the spread of flora and fauna from the peninsula. Wetlands, salt marshes, mangroves, and other swampy formations make up the uplands and submerged lands. Soil "The general soils in the Pelican Island Refuge are Canaveral-Captiva-Palm Beach, which is characterized by the gently sloping, somewhat poorly drained to moderately drained sandy soils with shell fragments, and McKee-Quartzipsamments-St. Augustine, which is characterized by level, somewhat poorly drained soils mixed with sand and shell fragments." Other soils include Canaveral Fine Sand, Quartzipsamments, Captiva Fine Sand, McKee Mucky Clay Loam, and Kesson Muck. Air quality Good air quality is vital for the refuge to maintain itself. A few problems dealing with air pollution are carbon monoxide, lead, nitrogen dioxide, ozone, particulate matter, and sulfur dioxide. The primary producers of these pollutants are vehicle emissions, power plants, and industrial activities. The Indian River Lagoon area is said to have good air quality. Sometimes occasional temperate increases can temporarily degrade the air quality below the accepted levels. Waterways The Indian River Lagoon stretches from Ponce de Leon south of Daytona Beach to Jupiter Inlet near West Palm Beach, a distance of about , and contains a number of small rivers, creeks, and canals. The Intracoastal Waterway is the deepest part of the Lagoon. St. Sebastian River and Turkey Creek provide freshwater to the Lagoon. Water quality is also a concern in the refuge: cadmium, lead, mercury, nutrients, selenium, thallium, and dissolved oxygen. The water circulation is affected by the Intracoastal Waterway, winds, inlets, and causeways. Within the refuge boundary, the water quality is generally better compared to portions of the Lagoon. Wildlife Pelican Island National Wildlife Refuge holds hundreds of species of animals including birds, fish, plants, and mammals. The wetlands of Pelican Island are a major ecological system supporting the huge biological diversity. Fifteen federally listed threatened and endangered species live in Pelican Island NWR and around Indian River Lagoon. Of the endangered species, West Indian manatees and sea turtles occupy parts of the lagoon. Around the lagoon in the refuge are two wood stork refuges. These birds along with other wading birds that nest on the island thrive on the tremendous fish population. Pelican Island is home to many nesting birds including brown pelicans, great egrets, snowy egrets, reddish egrets, great blue heron, little blue heron, tricolored heron, black-crowned night heron, American white ibis, glossy ibis, double-crested cormorant, anhinga, and American oystercatcher. Visiting Pelican Island is only accessible by boat or chartered tours. Nesting birds are easily disturbed, so people are not allowed to get too close or to disembark. Visiting during nesting season (late November through late July), one can expect to see brown pelican, wood storks, white ibises, black-crowned night herons, double-crested cormorants, reddish, snowy, and great egrets, and great blue, little blue and tricolored herons. Traveling in the winter, look for lesser scaup, blue-winged teal, mottled ducks, great northern divers, laughing gulls, American white pelicans, and red-breasted mergansers. Summer visitors should watch for roseate spoonbills, magnificent frigatebirds and least terns. Pelican Island also features some marine life in the Indian River including sea turtles, dolphins, and manatees. New public facilities were opened and dedicated on March 14, 2003, in ceremonies marking the centennial of Pelican Island and the National Wildlife Refuge System. A 37¢ US Commemorative Stamp in honor of the NWR Centennial was issued as part of the celebration. The new facilities include a 1/4 mile boardwalk and observation tower to view Pelican Island, two salt marsh impoundment foot trails, interpretive signs, informational kiosks, restrooms and parking areas. The facilities are west of Highway A1A on the north end of Historic Jungle Trail. They were produced through a partnership with Indian River County, St. Johns River Water Management District, Florida Inland Navigation District, Florida Power and Light, ConocoPhillips, Wild Birds Unlimited, the National Fish and Wildlife Foundation, and many others. Future plans include additional boardwalks, an overlook, a photo blind and a wildlife drive. Budget cuts Pelican Island, along with many other wildlife refuges, has been experiencing budget cuts. Many problems arise from the stagnant budget and lack of maintenance in the wildlife refuges. These are vital to preserve the habitat and the wildlife and to provide public education and recreation. This situation worsened further because of the failure of congress to timely pass federal funding bills. Staffing at Pelican Island is made up of U.S. Fish and Wildlife Service. The staff members have recently fallen from six to two which has had many negative consequences. The cuts have led to limiting refuge work and restricting public visitation. Another consequence is the end of 14-year tradition of the wildlife festival. Pelican Island will be losing its only public-use staff and eliminating all active outreach at the nation's first wildlife refuge. Pelican Island Refuge manager and project leader Paul Tritaik said in 2006 that reductions to a full-time staff would lead to the end of some refuge activities and the loss of several trails. See also Florida State Parks Indian River County, Florida List of National Wildlife Refuges History of the National Wildlife Refuge System Notes References Dinnage, Russell J. "WILDLIFE REFUGES: Budgetary downturn for national refuges hits staffers hardest." Land Letter. 16 November 2006. Hem, Brad. "Looking ahead, Pelican Island may be next in line: Port of Houston buys land, could join Galveston in a joint effort." The Houston Chronicle. 4 February 2007. McHugh, Paul. "Wildlife refuges on life support; Flat budgets imperil future of the system." The San Francisco Chronicle. 21 December 2006. "Parks: Pelican Island National Wildlife Refuge." GORP. 2007. 26 April 2007. <http://www.gorp.com/parks-guide/travel-ta-prime-hook-national-wildlife-refuge-pelican-island-national-wildlife-refuge-birdwatching-sidwcmdev_068511.html>. "Pelican Island National Wildlife Refuge: Comprehensive Conservation Plan." U.S. Fish and Wildlife Service. Sept 2006. 9 May 2007. <http://library.fws.gov/CCPs/pelicanisland_final.pdf>. "Pelican Island National Wildlife Refuge." U.S. Fish and Wildlife Service. 2007. 26 April 2007. <http://www.fws.gov/pelicanisland/>. External links Official Pelican Island National Wildlife Refuge website Pelican Island Webcam website Category:National Wildlife Refuges in Florida Category:Indian River Lagoon Category:Wetlands of Florida Category:National Register of Historic Places in Indian River County, Florida Category:National Historic Landmarks in Florida Category:Protected areas established in 1903 Category:Protected areas of Indian River County, Florida Category:Ramsar sites in the United States Category:Landforms of Indian River County, Florida Category:Islands of Florida Category:1903 establishments in Florida

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Children enjoy toys that can captivate their attention. A toy ball is a particular play item that has endured the test of time and remained a favorite with children of all ages (infants, toddlers, etc.). However, as with any child's toy, some intrinsic dangers must be avoided. According to the U.S. Consumer Product Safety Commission, small objects can easily be lodged in the airway of young children, creating a choking hazard. Thus, it is imperative to create toy balls that are increasingly safe for use by children. Furthermore, a toy ball is often constructed from more than one base component (e.g., two half-spherical (hemispherical) shells that may be attached together to form a substantially spherical shell) in order to form a spherical structure. If these components that are used to construct the toy balls also contain small parts, they may create additional choking hazards to children in the event they come free during use. Thus, the particular construction of the components making up the toy ball must be considered so as to ensure safe use by children. In addition, ancillary entertainment features are often incorporated into toy balls (e.g., figurines, rattling elements, fluids, etc.) in order to further captivate and hold a child's attention. Such ancillary features are intended to be stimulating and aesthetically pleasing so as to maintain the attention span of most children. It should be noted, however, that some of these ancillary entertainment features may be sufficiently small in size so as to pose a potential choking hazard to children. Children sometimes play in rough manner. Thus, toys should generally be constructed so as to minimize the risk of damage during the normal course of play. In the instant case, a toy ball is sometimes subjected to rough play. A toy ball is subject to a plethora of physical activities (e.g., being thrown, rolled, dropped, hit, batted, etc.). Should a toy ball be broken apart in the course of play, the contents within the ball would be exposed/set free and, as such, the freed contents may constitute a risk to the safety of children playing with the toy. Additionally, the broken toy would be rendered unfit for future use. Prior art toy balls typically are constructed from two shell halves mated together to form a seam along an equator of the toy ball. Such prior art toy balls are illustrated in U.S. Design Pat. No. 274,070 to Ma, U.S. Design Pat. No. 190,036 to Lakin, U.S. Design Pat. No. 314,598 to Capper et al. (illustrated in FIG. 1), U.S. Pat. No. 4,272,911 to Strauss, U.S. Pat. No. 2,519,248 to Hulbert, and U.S. Pat. No. 2,351,762 to Hoover. The method of affixing one shell half to another can include but are not limited to cementing, heat-sealing, ultrasonic welding, and dielectric welding. Still other toys have a substantially formed sphere, with an opening to insert an additional entertainment item, and are then capped to encapsulate the item within the sphere. An example of such a prior art toy ball is illustrated in U.S. Pat. No. 4,601,675 to Robinson. During rough play, the toy balls have an increased risk of breaking open. The toy balls found in the prior art are not inherently resistant to forces acting perpendicular to the seam running along the ball's equator. More specifically, the equatorial seam provides little resistance to a shearing force applied at the seam or to tensile forces acting on the two shells perpendicular to the seam. Thus, it would be desirable to provide toy balls with a greater factor of safety for children. In particular, it would be desirable to provide a toy ball that possesses additional strength to withstand shearing forces acting on the seam of the toy ball. Additionally, it would be desirable to provide a toy ball that possesses additional strength to withstand tensile forces acting on the two shells perpendicular to the seam. Such additional strength would enhance the intrinsic value of a toy by providing an additional level of safety for children. Furthermore, while the addition of an element to structurally strengthen the toy ball is desired, any such element should not detract from the aesthetically pleasing nature of the toy ball to a child. Thus, there exists a need for providing a toy ball that has a construction that adds strength to the ball's seam in order to prevent the toy ball from breaking open and exposing its contents to the child playing with the ball. Furthermore, any additional element incorporated into the construction of the toy ball should be generally aesthetically pleasing to a child. Providing such an arrangement that both increases the toy's safety and makes the toy more aesthetically desirable not only increases a child's enjoyment, but also increases the attractiveness of the toy to anyone concerned with the safety of children. This invention is directed generally to a toy ball with additional strength to resist forces in a tensile direction or shearing forces applied to a main seam. More specifically, this invention is directed to a toy ball having two shells (hemispherical or unequal in size) fused together forming a seam, the toy ball also having opposing end caps, each end cap capturing a portion of each shell to resist both shearing and tensile forces acting on the seam.

3.046875

3

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Chapter 17 Chapter 17 Chapter 17 Chapter 17 Chapter 17 Chapter 17 Summary Grief, Didion tells us, is never quite what we expect. Though we know that the people close to us will die, we don’t look beyond the days or weeks immediately following their deaths. We expect to be crazy and inconsolable, but we don’t imagine that we will be “literally crazy,” as Didion terms it, believing that we have the power to bring a lost loved one back. We expect that the funeral will be the greatest test of our strength, when in fact the funeral is soothing, thanks to the comfort of others and the meaningful nature of the event. The test comes in the weeks and months following, when the mourning person must face a profound loneliness and sense of meaninglessness, and must do so alone. As a child, Didion had been fearful of the idea of meaninglessness and found comfort in geology. The shifting and changing patterns of the earth seemed inevitable and permanent, a notion Didion linked to the Episcopal saying, “As it was in the beginning, is now and ever shall be, world without end.” For Didion, the earth’s abiding indifference was a comfort. While the destruction of human life might cause personal sorrow, the world would always continue. After she married and had a child, Didion found further comfort in domestic routines, such as cooking meals and setting the table. People dealing with grief think a great deal about self-pity, Didion asserts. Self- pity, though common, is a practice almost universally condemned by society. Didion had spent nearly all of her time with John after they married, and her frequent impulse to talk to him didn’t go away after he died. With no one to share her thoughts with, she turns into herself, and that intense self-focus leads naturally to self-pity. Though some people who have experienced loss claim to feel the presence of the deceased, Didion never does. On several occasions after John dies, she speaks to him as if he were there, but she knows that, as a writer, imagining their dialogue comes naturally to her. However, as she imagines the responses he might give to her questions, Didion realizes that, while she thought she knew all of John’s thoughts, she really only knew a fraction of them. Before his death, John frequently told her that if something happened to him she should stay in their apartment, keep her friends close, and marry again within the year. But neither John nor Didion really understood the implications of John’s command, as both were incapable of imagining life without the other. Didion says “marriage is time,” referring to the significance of their shared history. It is also, she says, “the denial of time,” because since she was twenty-nine Didion had always seen herself through John’s eyes. Now she must see herself through other people’s eyes, and it makes her feel considerably older. In death, she says, we mourn not only the loss of the loved one but also the loss of ourselves. Analysis Didion has begun to take stock of the past year and now attempts to understand and draw a set of coherent conclusions from her experiences. She realizes that the intensity of the shock she felt at John’s death and her subsequent deranged reactions were not only caused by the suddenness of her intense loss, but also because she was jarred to realize that her expectations about grief had been so misguided. On the surface, she had been able to function without breaking down or becoming hysterical. In reality, she had temporarily been mentally ill, able to press on only because she deluded herself into thinking that she could bring John back. Didion had not only been shocked by grief, but also by her reaction to her own grief. In dealing with John’s absence, Didion realizes how much she communicated with him on a daily basis and how all that energy has now been turned inward. This intense level of self-focus might also be called self-pity, she worries. However, this powerful self-concern is an inevitable consequence of losing someone with whom she shared such a strong, unique bond. Didion is not only coping with the loss of John, but also with the loss of their shared memory. Her sense of self had been largely founded on her relationship—not because she lacked a strong identity of her own, but because their emotional, intellectual, creative, social, domestic, and daily lives were so bound together. The loss of John forces Didion to evaluate who she is without him, a daunting task, since she has not thought of herself in that way for forty years. Didion’s general reluctance to engage in behavior she deems indulgent makes her attempt to understand herself as an individual separate from John feel like an act of “self-pity,” but it is a necessary part of the healing process. When Didion discusses meaninglessness, she isn’t talking about an absence of meaning. Instead, she describes a way of looking at the world with a proper sense of perspective, acknowledging that personal tragedy seems insignificant when compared to massive geological shifts. Changes that can seem huge or overwhelming seem small when viewed within a broader perspective. Didion recalls how the indifference of the natural world served as a comfort to Didion as a child. This might seem like a strange concept, since many people find comfort in exactly the opposite notion: that there is, in fact, a higher consciousness that cares about our personal welfare and benevolently controls our individual lives. However, Didion’s childhood worldview still has religious overtones, as she takes comfort in the idea that the world exists on such a huge scale that she, as a single human being, could never fully comprehend it entirely. For someone who always needs to be right and who fervently believes that research can answer all questions, acknowledging that there are things in the world that cannot be fathomed or understood, even through the most diligent inquisition, is a profound shift in thinking and an important step toward ending the process of magical thinking.

3.046875

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How to Help Language Impaired Students Improve their Leisure Skills Do you have students on your caseload who have very limited leisure skill interests? Are these students often left out of group activities at school and in the home environment? When our students do not engage in play/ leisure activities they are missing out on a natural way to work on language instruction. Read the following article, a guest post by Rosemarie Griffin from ABA Speech, to help your students increase their functional language and leisure skills: Leisure skills can be addressed in a variety of ways in clinic or school based settings. If you have a student who receives direct individual therapy, you could work on a specific leisure skill during therapy and generalize it to a larger group, when the student is able to engage in the skill with minimal prompts from an adult. Another way to target leisure skill instruction would be to teach a specific leisure skill (i.e. modified musical chairs) to a small group of students. It is important whether you are teaching the skill in an individual or small group session that the students know exactly how to engage in the skill. There are many evidenced based strategies, but we will focus on the skill of video modeling. Video modeling is a mode of teaching that uses video recording. The video recording acts as a visual model of the targeted skill or behavior. It can take many forms. The video can be of the student engaging in the skill or it can be of another individual engaging in the skill. The learner watches the video and then they perform the skill in the moment or at a later time. For example, if you are teaching students to play UNO® as a modified game; you could make a video of students playing this game the modified way ( i.e. matching just the color cards or playing minus the skip, reverse, wild and draw two). You would show the video to the students learning the game and then have them play the game. There is a lot of research that supports using this strategy to teach skills to individuals with autism and other disabilities. Below I will describe 2 modified leisure activities that I use with my middle school and high school students. A favorite of game of my students happens to be UNO®. There are 2 ways to modify UNO® based on the level of learner you have in your group. For early learners, you can lay out one card of each color on the table ( yellow, red, green, blue) and put the other cards face down. You each take a turn picking a card and matching it to the cards on the table. If your students are ready for more of a challenge you can play uno the regular way but without the skip, reverse, wild and draw two cards. This is such a popular game and one that many families have at home. It would be great to work on this at school and let the parents know about all of the work that you have done. Playing UNO® at home would be a wonderful way for your student to spend quality time with his family, while generalizing this leisure skill to new people and new environments. Another game that many of my students enjoy is playing Scrabble®. We each pick seven tiles and take turns making words on the board. The modification is that the words do not have to be connected in any way. This is what makes Scrabble® so difficult! I allow the students to make a word anywhere that they want on the board. If you have a student in the group who is having difficulty making a word on their own, grab a dry erase board and write down a word for them that they could make with their tiles. They can pick the tiles and match them to the word and transfer to the board. Viola a wonderful way to enjoy a cooperative group activity with students of varying ability levels. Being able to participate in age appropriate leisure skills gives students the opportunity to practice social language skills and helps them to feel more included with peers and their family members. Working on leisure skills can be enjoyable for all; I hope that these strategies will help you incorporate this instruction into your therapeutic practice. Rosemarie Griffin is a speech language pathologist, board certified behavior analyst and product developer. She is the creator of the Action Builder Cards. To learn more about modified leisure skills or to gather information about using applied behavior analysis to help students increase their communication skills, check out her website www.abaspeech.org or like her Facebook page here: ABA SPEECH ON FACEBOOK. Ms. Gardenia on Instagram Notice This website or its third-party tools use cookies, which are necessary to its functioning and required to achieve the purposes illustrated in the cookie policy. If you want to know more or withdraw your consent to all or some of the cookies, please refer to the Cookie Policy. By closing this banner, scrolling this page, clicking a link or continuing to browse otherwise, you agree to the use of cookies. By using our site, you acknowledge that you have read and understand our Cookie Policy, Privacy Policy, and our Terms of Service. Your use of this site's Products and Services are subject to these policies and terms.

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The regulations allow approximately 11.7 million instances of harassment, injury, or even death (the legal term is "take") to marine mammals by exposing them to high-intensity military sonar training in coastal waters around the United States. These estimates – the Navy's own – include 9.7 million takes along the Atlantic Coast and the Gulf of Mexico; 630,000 off the coast of southern California; 650,000 along the coast of Washington and Oregon; 140,000 in Hawaii; and another 500,000 off the coast of Florida. Sonar exposure is not, as the Navy suggests, a mere matter of annoyance to whales and dolphins. In fact, the harm ranges from significant disturbance to important behaviors – feeding, breeding, migrating, communicating, finding mates – to hearing damage and even mass stranding and death. At risk are not only some of the most vulnerable whale populations on Earth – including the last remaining 300 North Atlantic right whales and the 83 critically endangered southern resident killer whales off the Washington coast – but the very fabric of life among species that, over eons in the dark ocean, have evolved to depend on sound as we depend on sight. According to government scientists, the "loss of even a single individual right whale may contribute to the extinction of the species." In recent decades, a growing number of mass whale mortalities around the world have occurred in the shadow of military sonar training, in coastal waters as diverse as the Bahamas, the Canary Islands, Greece, North Carolina, Hawaii, Washington State, and many others. According to scientists – including the Navy's own consultants – there is no longer any doubt that sonar kills whales, whether by stranding or massive internal hemorrhaging – akin to what human divers experience as the "bends." Nor, as the Navy has argued, is sonar's impact a necessary consequence of securing our national defense. Most of the harm to marine mammals authorized by the Bush administration could be avoided by the use of common sense safeguards, many of which the Navy has used in past training exercises without apparent problem. Simple steps such as avoiding sensitive areas like marine sanctuaries, critical habitats, and feeding or breeding grounds; adopting adequate monitoring and safety zones around the sonar device; powering down in ocean conditions of particular acoustic risk; and implementing ship based, aerial, and underwater techniques to monitor when marine mammals are present enable a protective response. But for all of the recent proposed sonar training, the Navy has refused to implement any of this mitigation, instead proposing half-measures dismissed by the federal courts as "woefully inadequate and ineffectual." During the past decade, the courts have been the only effective line of defense against the Navy's needlessly dangerous sonar training, but litigation is piecemeal. A more effective, more comprehensive political response may now be possible. And given the geographic reach of the proposed sonar training and the Navy's own predictions of harm, such a response may be the only way to counter what amounts to an astonishing acoustic assault on marine life along all our coasts. New leadership is already in place at NOAA. New leadership, we hope, will soon be coming to the US Navy. Instead of the Bush administration's last-minute attack on whales and other marine life, the new administration should require a uniform protocol of effective safeguards for all Navy sonar training that would prevent the needless infliction of harm. We urge NOAA to move quickly and forcefully to exercise its authority – and fulfill its responsibility – to protect our oceans.

3.015625

3

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Epidemiology, Genetic Recombination, and Pathogenesis of Coronaviruses. Human coronaviruses (HCoVs) were first described in the 1960s for patients with the common cold. Since then, more HCoVs have been discovered, including those that cause severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome (MERS), two pathogens that, upon infection, can cause fatal respiratory disease in humans. It was recently discovered that dromedary camels in Saudi Arabia harbor three different HCoV species, including a dominant MERS HCoV lineage that was responsible for the outbreaks in the Middle East and South Korea during 2015. In this review we aim to compare and contrast the different HCoVs with regard to epidemiology and pathogenesis, in addition to the virus evolution and recombination events which have, on occasion, resulted in outbreaks amongst humans.

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Opaque, white steam trailing behind loud trucks were a routine sight in many a childhood around the world. In South Korea, too, trucks would wail out siren sounds while emitting disinfectants and children would chase after the trucks through narrow alleyways, breathing in the foul-smelling gas. Used as a pesticide against mosquitoes and larvae, as well as a general means to prevent infectious disease, these disinfectants have remained a regular part of national public health measures since the mid-1900s. But within the past decade, these trucks have become increasingly difficult to catch in the streets of South Korea. A video posted by a South Korean user, chasing after a disinfecting truck (Source: YouTube) Traditional smoke disinfectant is effective in its ability to rapidly disinfect large areas. And its explicitly loud, smoke-spewing nature does more than give young children something fun to do — according to the Gwangjin-gu Public Health Center in Seoul, one of its advantages is that “its visible nature leads to citizen support.” But smoke disinfectant — made by diluting kerosene or heavy oil with insecticide and sprayed with a heater — affects an unpredictable radius. This can lead to unexpected health risks to residents in nearby housing areas, according to a 2015 Ministry report from the Ministry of Health and Welfare. Smoke disinfectants include chemicals dangerous to the environment. For example, when oils are not completely combusted, the resulting solution contains volatile compounds such as belen, toluene and other carcinogens that can be harmful to both people and the environment. Just last year, Busan, South Korea’s second largest city with a population of three million, announced efforts to increase environmentally friendly solutions with an investment of 500 million won, according to daily newspaper Busan Ilbo. While the traditional disinfectant is still necessary for hard-to-access areas such as sewers, the ultimate goal is to reduce the use of smoke disinfectant from 72 to 25 percent. Citizens and governmental agencies have become more cognizant of potential dangers, calling either for a ban or changes to trucks spraying disinfectant gases. The Ministry of Health and Welfare said that it recommends, instead of excessive smoke disinfectant, spray methods or targeting larvae before they develop. With new technologies and increased health concerns, the nostalgia-inducing images of smoke trailing behind a blaring truck are surely becoming much more of a rarity. But that doesn’t mean they’ve stopped entirely, nor will they any time soon. In 2005, daily newspaper Hanykoreh reported that of 246 public health centers across the country, 239 — practically all of them — were using smoke disinfectant. Seven years later, Hankoyreh conducted another similar study (although this time with far fewer centers) and found that 23 out of 36 public health centers contacted across the country still planned to use smoke disinfectant. Though the traditional oil-based smoke disinfectants are far from extinct, many of the centers in the recent study are showing efforts, such as water-based solutions, to become more environmentally friendly. And as public health centers seek out new, safer mixtures, in response to rising public awareness about the possible dangers of these trucks, health measures are shifting — from what was once an explicit, loud display of communal cleaning into a humbler national effort to do the same job but maybe in a safer way. Cover image: Though less common now, mosquito trucks spewing disinfectant smoke have long been a common sight in South Korea. (Source: YouTube)

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Wouldn't it be great if, when landing a robotic mission on another planet, the lander or rover could just scoop a sample, drop it into a chemical analyzer and get a "positive" or "negative" result for extraterrestrial life? Well, this chemistry test isn't so far fetched and scientists at NASA's Jet Propulsion Laboratory in Pasadena, Calif., are working on a method that is 10,000 times more sensitive than any other method currently employed by spacecraft. Focused on the detection of specific types of amino acid tied to life, the researchers propose mixing a liquid sample collected from the surface of an alien world with a chemical known as a liquid reagent. Then, by shining a laser across the mixture, the molecules it contains can be observed moving at different speeds when exposed to an electric field. From this, the different molecules can be identified and the whole thing can be done autonomously, no humans required. The method known as "capillary electrophoresis" can be used to detect many different types of amino acids simultaneously. "Our method improves on previous attempts by increasing the number of amino acids that can be detected in a single run," said researcher Jessica Creamer in a statement. "Additionally, it allows us to detect these amino acids at very low concentrations, even in highly salty samples, with a very simple 'mix and analyze' process." RELATED: Stormy Alien Atmospheres May Spark Seeds of Life The team has already tested the method on water taken from Mono Lake in California - a mass of salty water with an extreme alkalinity - and simultaneously analyzed 17 different amino acids. "Using our method, we are able to tell the difference between amino acids that come from non-living sources like meteorites versus amino acids that come from living organisms," said Peter Willis, the project's principal investigator also at JPL. Molecules like amino acids come in two different "chiralties" that are mirror images of one another. Non-organic sources contain roughly equal "left-" and "right-handed" chirality amino acids, whereas amino acids from living organisms are predominantly left-handed - for life on Earth in any case. This differentiation can be detected by capillary electrophoresis. This method is exceedingly powerful for several reasons. Currently, NASA is putting great efforts into looking for habitable environments on Mars. We know that the Red Planet used to be a very wet place and there's evidence that suggests very briny sources of liquid water exists to this day. If life has ever taken hold on Mars, and if a future mission can directly sample this salty, toxic water, it's sensitive chemical analyses such as this that will likely track it down. Also, in the future, it is hoped that a mission may be sent to Jupiter's moon Europa, which is known to possess an extensive subsurface ocean. Many components for life as we know it exists on Europa, so if a robotic mission can be sent to the moon's ice-encrusted surface, or even dropped into the ocean itself, finding out whether there's life elsewhere in the solar system could be one simple chemistry test away. WATCH VIDEO: Could Life On Earth Have Come From A Comet?

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INTRODUCTION ============ *Helicobacter pylori*, a Gram-negative human pathogen, colonizes the stomach and is associated with several gastrointestinal disorders including peptic ulcers and gastric cancers ([@B1]). Over half of the world\'s population is estimated to harbor *H. pylori*, but only 15--20% of those infected develop severe disease. *Helicobacter pylori* is known for its remarkably high level of genetic diversity. A comparison of the fully sequenced genomes of three clinical isolates revealed substantial differences in chromosomal structure and a large number of genes that are variably present or absent among strains (up to 25% of the total coding regions) ([@B2],[@B3]). These observations have raised many questions, including how genetic diversity is generated in *H. pylori* and how variable genes contribute to disease outcome. One class of highly variable genes are restriction--modification (R--M) systems ([@B2]), which are typically composed of both a restriction endonuclease (REase) and a cognate DNA methyltransferase (MTase). Generally, the REase cleaves a specific DNA sequence unless it is methylated by the cognate MTase. R--M systems have been divided in type I, II or III, according to their cofactor requirement, molecular structure, mode of action and structure of the recognition sequence site ([@B4]). Typical type II R--M systems consist of two independent enzymes that act on the same sequence, usually a 4- to 8-bp palindrome. The recent sequencing of more than 400 bacterial and archaeal genomes has revealed that ∼90% of the genomes contain at least one R--M system and over 80% contain multiple R--M systems ([@B5]), but only a small fraction have been comprehensively studied. The *H. pylori* chromosome encodes a large number of active and inactive R--M systems. Analysis of the sequenced genomes of *H. pylori* strain 26695 and J99 predicted 26 putative R--M systems including 14 and 16 type II R--M systems, respectively. Comparative genomics of these systems suggests they have a high degree of sequence heterogeneity and that only a small fraction retained full activity ([@B6],[@B7]). Interestingly, for some R--M systems, MTase activity may be preserved despite inactivation of the respective REase. Although still under debate, R--M systems may carry out several biological roles. They have traditionally been implicated in bacterial defense from bacteriophage infection, which have in turn evolved a variety of anti-restriction defense mechanisms ([@B8]). R--M systems also regulate genetic exchange among bacteria, particularly relevant for bacteria like *H. pylori* that are naturally competent for DNA uptake ([@B9]). By constituting an effective barrier against DNA transformation in a bacterial population, R--M systems may provide the genetic isolation required for adaptation of the organisms to a special ecological niche ([@B10]). Paradoxically, R--M systems were also suggested to promote homologous recombination from the small DNA fragments produced by the incomplete digestion of incoming DNA by REases ([@B11]). Kobayashi and colleagues have suggested that R--M systems have attributes of selfish genes, and may act as invasive elements independent of any selective advantage to their host ([@B12],[@B13]). This hypothesis emerged from the findings that several R--M systems are horizontally transferred and that a fully active type II R--M system cannot easily be lost from its host because of postsegregational killing. Finally, DNA methylation may have important biological properties independent of the endonuclease function by regulating the interactions between proteins and DNA, in a similar manner to the stand-alone DNA methyltransferase Dam in both α- and γ-Proteobacteria ([@B14],[@B15]). In *H. pylori*, R--M systems may carry out other biological roles. Several R--M systems have been classified as 'chronic atrophic gastritis (ChAG) associated genes' by comparing the genome content of eight ChAG strains to a *H. pylori* 'pangenome' defined previously ([@B3],[@B16]). Other R--M genes were acid-regulated ([@B3]), undergo phase variation ([@B17],[@B18]) and several R--M systems were identified as candidate colonization factors using a mouse model of infection ([@B19]). Expression of the REase encoded by gene *iceA1* was upregulated upon contact with gastric epithelial cells and its presence was associated with peptidic ulcer disease ([@B20]). A mutant in the endonuclease R.HpyC1I, isolated from *H. pylori* clinical isolate NTUH-C1, exhibited cell elongation and decreased adherence to a gastric cell line ([@B21]). In another report, DNA methylation by M.HpyAIV was shown to alter transcription of a selected number of genes including catalase (*katA*) ([@B22]). Here, we annotate a previously uncharacterized *H. pylori* R--M system M.HpyAXII/R.HpyAXII encoded by the locus HP0502/0503/0504/0505. We present biochemical and genetic analyses of this R--M system. We additionally explored its conservation among clinical isolates and its role during establishment of infection to query alternative biological functions of M.HpyAXII/R.HpyAXII. MATERIALS AND METHODS ===================== Bacterial strains and growth conditions --------------------------------------- *Helicobacter pylori* strains ([Supplementary Table S1](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)) were grown on solid horse blood agar (HB) plates containing 4% Columbia agar base (Oxoid, Hampshire, UK), 5% defibrinated horse blood (HemoStat Labs, Dixon, CA), 0.2% β-cyclodextrin (Sigma, St Louis, MO), 10 µg/ml vancomycin (Sigma), 5 µg/ml cefsulodin (Sigma), 2.5 U/ml polymyxin B (Sigma), 5 µg/ml trimethoprim (Sigma) and 8 µg/ml amphotericin B (Sigma) at 37°C either under a microaerobic atmosphere generated using a CampyGen sachet (Oxoid) in a gas pack jar or in an incubator equilibrated with 14% CO~2~ and 86% air. For liquid culture, *H. pylori* was grown in Brucella broth (Difco, Franklin Lakes, NJ) containing 10% fetal bovine serum (BB10; Invitrogen, Carlsbad, CA) with shaking in a gas pack jar containing a CampyGen sachet. For resistance marker selections, bacterial media were additionally supplemented with 15 µg/ml chloramphenicol (Cm, Sigma), 25 µg/ml kanamycin (Kan, Fisher Scientific, Pittsburgh, PA) or 60 mg/ml sucrose (Fisher Scientific). When culturing bacteria from mouse stomachs, 200 μg/ml bacitracin (Sigma) was added to eliminate normal mouse microbiota contamination. DNA manipulations ----------------- DNA manipulations, such as restriction digestion, PCR and agarose gel electrophoresis, were performed according to standard procedures ([@B23]). *Helicobacter pylori* genomic DNA was prepared by Wizard genomic DNA preparation kits (Promega, Madison, WI). Primers used for PCR and sequencing are in [Supplementary Table S2](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1). Plasmid DNA ([Supplementary Table S3](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)) was isolated and prepared from *Escherichia coli* or *H. pylori* using Qiagen Midiprep kit (Qiagen, Valencia, CA). Sequencing of plasmid DNA and PCR products was performed by the FHCRC Genomics Shared Resource and the resulting sequences analyzed using Sequencher (Gene Codes Corporation, Ann Harbor, MI). Generation of *H. pylori* knockout isogenic mutants --------------------------------------------------- Knockout alleles were constructed using a vector-free allelic replacement strategy to generate alleles in which a chloramphenicol acetyl transferase (*cat*) resistance cassette ([@B24]), a nonpolar kanamycin resistance (*aphA3*) cassette ([@B25]), or a *cat* cassette fused to a sucrose sensitivity marker (*sacB*) ([@B26]) replaced 80--90% of the coding sequence of the gene while preserving the start and stop codons. The primers used for this procedure are designated as 1 through 4 and are given in [Supplementary Table S2](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1). The *catsacB* cassette was generated by fusing *cat* to *sacB* with elimination of the terminator sequence using PCR (primers C2SA4 and SB1). After natural transformation ([@B27]) with the appropriate PCR product and selection on Cm- or Kan- containing media, four clones were evaluated by PCR to confirm replacement of the wild-type allele with the null allele. Urease activity and flagella-based motility were also confirmed for all the clones generated. Single clones were used for infection experiments and phenotypic characterization. Generation of *H. pylori* knockin isogenic mutants -------------------------------------------------- Null alleles generated by replacement with the *catsacB* cassette were subsequently replaced with alternate alleles by sucrose counter-selection. *H. pylori* strain NSH57 Δ*hpyAXIIM/R::catsacB* was naturally transformed with the appropriate plasmid or genomic DNA, and recombinants were selected on sucrose-containing HB plates, screened on Cm-containing media, and evaluated by PCR to confirm they lost the *catsacB* cassette. Site-directed mutagenesis ------------------------- To generate a catalytically inactive DNA MTase in *H. pylori* strain NSH57, an asparagine in conserved motif IV was replaced by alanine (N87A). A DNA fragment including *hpyAXIIM/R* was amplified from NSH57 by PCR and cloned into TA vector pCR-TOPO (TOPO cloning, Invitrogen). pCR-TOPO/*hpyAXII* was digested with EcoRI (NEB, Ipswich, MA) and subcloned into plasmid Bluescript SK+ (Stratagene, La Jolla, CA). Site-directed mutagenesis was performed on *hpyAXIIM* using the QuikChange kit (Stratagene) following the manufacturer instructions and confirmed by sequencing. Natural transformation ---------------------- *H. pylori* bacteria were freshly grown for 24--32 h on HB plates, transferred as patches onto fresh plates and grown for an additional 6--8 h. Donor DNA (plasmid, genomic or PCR product) was diluted as appropriate in distilled water and 10 μl was added to each patch and incubated overnight. The transformation mixture was harvested from the plate surface and resuspended in 350 μl phosphate buffer saline (PBS). Serial 10-fold dilutions were inoculated onto selective or nonselective HB plates. Transformation frequency was calculated as the number of Kan or Cm resistant colonies per recipient cell per nanogram of donor DNA. Expression of M.HpyAXII and R.HpyAXII proteins ---------------------------------------------- *hpyAXIIM* was amplified from DNA of wild-type NSH57 and NSH79 *H. pylori* by PCR and cloned into a pET-15b vector (Novagen, Gibbstown, NJ) in frame with the N-terminal His-Tag sequence using NdeI and XhoI (New England Biolabs). The resulting pET15b/*hpyAXIIM* plasmids were transformed into *E. coli* strain ER2925(DE3), derived from strain ER2925 \[NEB and ([@B28])\] and engineered to become a λDE3 lysogen using a lysogenization kit (Novagen). Plasmid pET15b/*hpyAXIIR* was transformed into *E. coli* strain BL21CodonPlus(DE3)-RIL. Protein expression was induced using 1 mM isopropyl-1-thio-β-[d]{.smallcaps}-galactopyranoside (IPTG) induction for 3 h at 37°C for M.HpyAXII and overnight at 16°C for R.HpyAXII to minimize endonuclease activity. Bacterial pellets were resuspended in lysis buffer (50 mM Tris pH 7.9, 100 mM NaCl, 1 mM DTT, 2% glycerol), incubated with 1 mg/ml lysozyme (Sigma) for 30 min on ice, and sonicated. For R.HpyAXII, soluble and insoluble fractions were separated by centrifugation at 18 000 r.p.m. for 20 min at 4°C. Antibody-based M.HpyAXII methylation activity assays ---------------------------------------------------- M. HpyAXII DNA MTase activity was assessed in a dot-blot assay using a rabbit primary antibody raised against DNA with N6-methyladenine (m6A) ([@B29]). *Escherichia coli* ER2925(DE3) transformed with pET15b and pET15b/*hpyAXIIM* was grown to log phase and induced with 1 mM IPTG for 3 h at 37°C. Genomic DNA of the cultures was isolated and 3 μl cross-linked to a nylon membrane (Hybond-XL, Amersham Biosciences, Piscataway, NJ) by UV (1.2 mJ/cm^2^ for 30 s). The membrane was blocked in a 3% nonfat dry milk solution and incubated with the m6A polyclonal rabbit antibody (1:10 000 dilution) overnight at 4°C. After a series of washes in PBST (PBS and 0.1% Tween-20), anti-rabbit IgG antibody conjugated to horseradish peroxidase (1:1000 dilution) was added to the membrane and detected using ECL Western Blotting reagent (Amersham Biosciences). Biochemical R.HpyAXII endonuclease activity assay ------------------------------------------------- One microliter of freshly prepared soluble fraction obtained from *E. coli* BL21(DE3) expressing R.HpyAXII was incubated for 3 h at 37°C with 500 ng *E. coli* ER2925 genomic DNA or pET15b plasmid DNA isolated from *E. coli* DH10B in presence of NEB buffer 1 (New England Biolabs). The product DNA was separated on a 0.8% agarose gel. Genetic R.HpyAXII endonuclease activity assay --------------------------------------------- To assess R.HpyAXII activity in a large number of *H. pylori* strains, we replaced the null allele in *H. pylori* strain NSH57Δ*hpyAXIIM/R::catsacB* with that from other strains as described above (Generation of *H. pylori* knockin isogenic mutants section**)**. R.HpyAXII activity was determined by transforming these *H. pylori* clones with PCR constructs Δ*hpyXIIM::cat* and ΔHP0368::*cat* and enumerating recombinants recovered on Cm- containing HB plates. Mouse infections ---------------- Female C57BL/6 mice 24- to 28-days old were obtained from Charles River Laboratories and certified free of endogenous *Helicobacter* infection by the vendor. The mice were housed in sterilized microisolator cages with irradiated PMI 5053 rodent chow, autoclaved corn cob bedding, and acidified, reverse-osmosis purified water provided ad libitum. All studies were done under practices and procedures of Animal Biosafety Level 2. The facility is fully accredited by the Association for Assessment and Accreditation of Laboratory Animal Care, International, and all activities were approved by the FHCRC Institutional Animal Care and Use Committee. Competition experiments were performed as described previously ([@B24]) with 5.0 × 10^8^ bacteria of each strain in the inocula. *In silico* genomic analysis ---------------------------- *Helicobacter pylori* sequences were retrieved from the Comprehensive Microbial Resource (CMR) ([@B30]). Homologs of M. and R.HpyAXII and were sought using REBASE Blast, a tool of REBASE ([@B5]). Protein structure prediction analysis for M.HpyAXII and R.HpyAXII was carried out using the Protein Homology/Analogy Recognition Engine PHYRE ([@B31]). Sequence alignments were carried out with CLUSTALW2 ([@B32]) and 3D molecular structures were visualized and modified using PyMOL ([@B33]). The genome-wide distribution and frequency of GTAC sites was determined using genome-scale DNA pattern in Regulatory Sequence Analysis (RSA) Tools (<http://rsat.ulb.ac.be/rsat/>). For *H. pylori* strain NSH57, the sequence of the derivative strain G27 was used (D.A. Baltrus, M.R. Amieva, A. Covacci, D.S. Merrell, K. M. Ottemann, M. Stein, N.R. Salama, K. Guillemin, personal communication) and genomic GTAC sites were analyzed with the genome tools/restriction digest option of the CMR website. Sequences are available from the GenBank/EMBL/DDBJ databases with accession numbers FJ233107 to FJ233133. RESULTS ======= Structure-based prediction uncovers the existence of a novel *H. pylori* R--M system ------------------------------------------------------------------------------------ We set out to further characterize the HP0502/0503/0504/0505 locus that we previously identified in our genome-wide screen for candidate colonization factors ([@B19]). BLAST search of DNA sequences of these genes from *H. pylori* strain 26695 failed to identify any homologs. However, several lines of evidence suggested that HP0502/0503 encodes a DNA MTase and that it is organized in an R--M system along with the downstream gene, HP0504/0505. Nobusato *et al.* ([@B7]) previously predicted that this locus encodes a R--M system based on sequence analysis. In agreement with this finding, we used structure prediction algorithms of the program PHYRE ([@B31]) and found that the N-terminal domain of the HP0502/0503 polypeptides could be threaded onto a tertiary structure of the M.TaqI DNA MTase, crystallized from *Thermus aquaticus* ([Supplementary Figure S1](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1), *E*-value 6.1 × 10^−15^). Despite weak protein sequence homology, several amino acid motifs were shared between HP0502/0503 and M.TaqI ([Figure 1](#F1){ref-type="fig"}A) and mapped to the catalytic domain of M.TaqI ([Supplementary Figure S1](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)), further supporting the function of HP0502/0503 as an adenine MTase ([@B34]). More recently, the REase R.PabI from *Pyrococcus abyssi* was characterized and HP0504/0505 was identified as a homolog (28% protein sequence identity) and suggested to recognize the same target sequence, 5′-GTAC-3′ ([@B35]). Based on the proposed nomenclature for R--M systems ([@B4]), we have named this novel *H. pylori* R--M system M.HpyAXII/R.HpyAXII, encoded by genes *hpyAXIIM* and *hpyAXIIR*, respectively. Since R--M systems are highly polymorphic among *H. pylori* strains ([@B6]), we evaluated the genomic organization of M.HpyAXII/R.HpyAXII in several isolates. As illustrated in [Figure 1](#F1){ref-type="fig"}B, gene *hpyAXIIM* encodes a polypeptide of 331 amino acids and is predicted to be active in strains J99, HPAG1 and NSH57 but is likely inactive in 26695 and NSH79 where the expected protein products are truncated and fused with R.HpyAXII, respectively. Gene *hpyAXIIR* encodes a protein of 252 amino acids and is only expected to be functional in strains J99 and HPAG1 based on DNA sequences. Figure 1.Genomic organization of the HpyAXII R--M system. (**A**) Amino acid sequence alignment of 26695 HP0502/0503, NSH57 M.HpyAXII and M.TaqI from *Thermus aquaticus* reveals conserved motifs (highlighted in gray) in the N-terminal portion of the protein. (\*) - identical residues, (:) conserved substitution, (.) semi-conserved substitution. (**B**) Genomic organization of genes *hpyAXIIM* and *hpyAXIIR* in *H. pylori* strains 26695, J99, HPAG1 and two mouse adapted strains NSH57 and NSH79. The expected phenotype for this R-M system in each strain is given based on DNA sequences. M, DNA MTase; R, REase; +, active; --, inactive. M.HpyAXII is truncated in 26695 and fused to R.HpyAXII in NSH79. R.HpyAXII is truncated in 26695, partially deleted in NSH57 (dashed lines), and fused to M.HpyAXII in NSH79 (in-frame deletion represented with dashed lines). M.HpyAXII functions as a γ-adenine MTase ---------------------------------------- To validate the function of M.HpyAXII as a DNA MTase, we inducibly expressed Histidine-tagged M.HpyAXII from *H. pylori* strain NSH57 and Histidine-tagged M.HpyAXII fused to R.HpyAXII from strain NSH79 in *E. coli* ([Figure 2](#F2){ref-type="fig"}A). M.HpyAXII activity was studied using *E. coli* strain ER2925(DE3) ([Supplementary Table S1](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)), defective for all known R--M systems, and presumably harboring chromosomal DNA devoid of adenine or cytosine methylation (Materials and methods section). Genomic DNA from the *E. coli* cultures expressing M.HpyAXII was isolated and adenine methylation assessed using antibodies against N6-methyladenine. Adenine MTase activity could be detected when M.HpyAXII from NSH57 but not NSH79 was expressed in *E. coli* ([Figure 2](#F2){ref-type="fig"}B). The lack of MTase activity by NSH79 M.HpyAXII probably reflects the genetic rearrangements observed at the NSH79 locus ([Figure 1](#F1){ref-type="fig"}B). To further confirm that M.HpyAXII acts as an adenine MTase, we used site-directed mutagenesis on the predicted catalytic site of this enzyme. We identified conserved motif IV (D/N/S)PP(Y/F) \[[Figure 1](#F1){ref-type="fig"}A and ([@B34])\] and the substitution of asparagine with alanine (point mutation designated N87A) in NSH57 M.HpyAXII completely abolished adenine MTase activity without affecting the expression levels of this protein ([Supplementary Figure S2](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)). Along with our genomic data, this finding supports the re-annotation of this *H. pylori* protein as a γ-adenine MTase. Figure 2.Biochemical demonstration that HypAXII functions as an R--M system targeting GTAC sites. (**A** and **B**) NSH57 M.HpyAXII methylates genomic DNA on adenines when expressed in *E. coli*. (A) *Escherichia coli* ER2925(DE3) extracts expressing NSH57 or NSH79 M.HpyAXII (arrowheads) separated by SDS--PAGE gel and stained with Coomassie blue. Control - empty plasmid. Two separate *E. coli* clones (1 and 2) were analyzed. (B) The indicated amount of genomic DNA from the respective *E. coli* cultures was cross-linked to a nitrocellulose membrane. DNA N-6 adenine methylation (m6A) was detected using anti-m6A antibodies and showed a signal during NSH57 M.HpyAXII but not NSH79 M.HpyAXII expression. (**C--F)** The HpyAXII R--M system targets the tetramer 5′-GTAC-3′. (C) *Helicobacter pylori* strain NSH57 wild-type and Δ*hpyAXIIM* genomic DNA was isolated and digested with RsaI. Agarose gel separation showed fragmentation for Δ*hpyAXIIM* genomic DNA but not wild-type. (D) *hpyAXIIR* from *H. pylori* strain HPAG1 was cloned and expressed *E. coli* BL21(DE3) under inducible conditions. Soluble (sol) and insoluble (insol) fractions were separated by SDS--PAGE gel and stained with Coomassie blue. R.HpyAXII was mostly insoluble (arrowhead). Control, empty plasmid. The soluble fractions shown in C were incubated with unmethylated genomic DNA (E) or plasmid DNA (F) and separated by agarose gel. DNA fragmentation was only observed when R.HpyAXII was expressed. Similar DNA restriction patterns (F) indicate that these enzymes cleave the same DNA sequence. Bands of higher sizes seen for with R.HpyAXII suggest incomplete digestion. Two separate *E. coli* clones are shown (1 and 2). The HpyAXII R-M system targets the tetramer 5′-GTAC-3′ ------------------------------------------------------ Two independent approaches defined the target sequence of this novel R--M system. First, using an array of methylation-sensitive endonucleases, we sought to identify an enzyme that could digest *H. pylori* NSH57 chromosomal DNA isolated from a Δ*hpyAXIIM* mutant but not from wild-type. Only the enzyme RsaI digested DNA from the Δ*hpyAXIIM::cat* mutant but not wild-type ([Figure 2](#F2){ref-type="fig"}C), indicating that the DNA MTase M.HpyAXII and the endonuclease RsaI act on the same target sequence, 5′-GTAC-3′, where the adenine residue is methylated by M.HpyAXII. Using this result, we investigated M.HpyAXII activity in the *H. pylori* strains where the HpyAXII R-M system was sequenced ([Figure 1](#F1){ref-type="fig"}B). Genomic DNA from *H. pylori* strains 26695 and NSH79 could be digested with RsaI, whereas J99, NSH57 and HPAG1 DNA were protected from RsaI digestion (data not shown), indicating that M.HpyAXII is only active in these three strains and agreeing with our predictions from the genomic sequences. RsaI digestion of DNA isolated from the NSH57*hpyAXIIM*^N87A^ mutant showed fragmentation when separated on agarose gel (data not shown), confirming that this single amino acid substitution abolishes MTase catalytic activity. In the second approach, we cloned and expressed the putative endonuclease gene *hpyAXIIR* in *E. coli* under the control of an inducible promoter ([Figure 2](#F2){ref-type="fig"}D). We chose *hpyAXIIR* from *H. pylori* strain HPAG1 because this protein is expected to be functional based on sequence analysis ([Figure 1](#F1){ref-type="fig"}). Incubation of the *E. coli* soluble fraction expressing HPAG1 R.HpyAXII with genomic DNA unmethylated for GTAC sites showed endonuclease activity as indicated by the resulting smear on agarose gel ([Figure 2](#F2){ref-type="fig"}E). To determine R.HpyAXII cleavage site, the same experiment was carried out with unmethylated plasmid DNA. R.HpyAXII-containing extract cleaved plasmid DNA and gave an identical fragmentation pattern as RsaI ([Figure 2](#F2){ref-type="fig"}F) confirming that R.HpyAXII acts on GTAC sites. In contrast to HPAG1 R.HpyAXII, no endonuclease activity was detected when R.HpyAXII from *H. pylori* strain J99 was expressed in *E. coli* (data not shown). While the exact cutting site of R.HpyAXII within the tetramer GTAC remains to be defined, our demonstration that *hpyAXIIM* and *hpyAXIIR* encode two independent enzymes suggests that they together constitute a class II R-M system ([@B4]). GTAC sites are scarce in the *H. pylori* chromosome but are found at high frequency in the rDNA genes ----------------------------------------------------------------------------------------------------- We determined the frequency and distribution of GTAC sites in four sequenced strains of *Helicobacter pylori*: 26695 (122 sites), J99 (184 sites), HPAG1 (114 sites), G27 (115 sites). This total number of sites is \>50-fold lower than the expected number based on frequency of nucleotides and confirms previous observations ([@B35]). Interestingly, a significant fraction of the GTAC sites are located within the ribosomal RNA (rRNA) genes. The 23SrRNA contains eight or nine sites depending on the strain analyzed and the 16SrRNA contains two sites ([Table 1](#T1){ref-type="table"}). Since two copies of each gene exist in the *H. pylori* chromosome, a total of 20 or 22 GTAC sites are located within the rRNA genes. We were particularly interested in GTAC sites that are strictly conserved among *H. pylori* strains since they may be biologically important. Of all intragenic sites, ten are conserved in all four *H. pylori* strains and can be mapped to a total of 10 genes that belong to various functional categories ([Table 1](#T1){ref-type="table"}). Interestingly, three of these genes belong to the cag pathogenicity island (*cagT*, *cagL* and *cagH*). Some of these sites are located in the promoter region of genes and may influence transcription efficiency. Table 1.Distribution of all conserved GTAC sites in four *H. pylori* strainsGene number[^a^](#TF1){ref-type="table-fn"}Gene name[^a^](#TF1){ref-type="table-fn"}Gene descriptionCharacteristics[^b^](#TF2){ref-type="table-fn"}23S rDNARibosomal DNA8 sites16S rDNARibosomal DNA2 sitesHP0200*rpl32*Predicted ribosomal protein L328 bp after start of HP0200 and 200 bp from start of HP0201HP0486*hofC*Outer membrane proteinHP0499*pldA*Phospholipase A1 precursorHP0532*cagT*cag pathogenicity island protein THP0539*cagL*cag pathogenicity island protein L200 bp from start of cagIHP0541*cagH*cag pathogenicity island protein HHP0613Predicted ABC transporter87 bp after start of HP0613HP0630*mda66*Modulator of drug activity11 bp after start of HP0630 and 170 bp from start of HP0631HP1197*rps12*Predicted ribosomal protein S12190 bp from start of HP1198HP1228*invA*Diadenosine polyphosphate hydrolase50 bp from start of HP1229[^1][^2] The HpyAXII R-M system effectively restricts incoming plasmid DNA ----------------------------------------------------------------- Bacterial R--M systems protect host genomes from invading DNA such as viral, plasmid and other foreign DNA by cleaving exogenous DNA at specific sites when unmethylated. We determined whether the endonuclease R.HpyAXII could restrict incoming plasmid DNA during natural transformation of *H. pylori*. As shown above, R.HpyAXII is biochemically active in *H. pylori* HPAG1, a strain difficult to transform (data not shown). We thus replaced the endogenous locus encoding M.HpyAXII/R.HpyAXII in the easily transformable NSH57 strain with that from HPAG1 (Materials and methods section). This engineered strain, NSH57*hpyAXIIM/R*~HPAG1~, encodes a fully active HpyAXII R-M system (R + M + phenotype). For comparison, we deleted the endonuclease component R.HpyAXII in the same strain and replaced it with an antibiotic resistance cassette to create a null allele (Δ*hpyAXIIR::aphA3*, R--M + phenotype). As donor DNA, we used plasmid pTM113-*cat* (Materials and methods and [Supplementary TableS3](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)) that we isolated from *H. pylori* strain NSH57 wild-type (fully methylated, denoted 'M+'), from the catalytically inactive mutant NSH57*hpyAXIIM*^N87A^ (unmethylated for GTAC sites, denoted 'M−'), or from *E. coli* (unmethylated at all sites, denoted 'all M−'). We first verified that the numerous R--M systems encoded by *H. pylori* strain NSH57 could effectively restrict unmethylated (all M−) plasmid DNA as compared to methylated (M+) plasmid. Transformation frequency of wild-type *H. pylori* NSH57 decreased over 200-fold when completely unmethylated plasmid DNA prepared from *E. coli* was used as compared to methylated (M+) plasmid (data not shown), in agreement with previous work ([@B37]). We similarly found that transformation frequency involving M− plasmid decreased over 60-fold in the bacteria harboring an active R.HpyAXII endonuclease (R+) (ratio R−/R+, [Table 2](#T2){ref-type="table"}), demonstrating that this enzyme constitutes an effective barrier against incoming plasmid DNA *in vivo*. Table 2.R.HpyAXII effectively restricts incoming plasmid DNADonor DNA[^a^](#TF3){ref-type="table-fn"}Transformation frequency (\# transformants/recipient cell/ng × 10^−8^)[^b^](#TF4){ref-type="table-fn"}, mean (SEM)RatioRecipient strain[^c^](#TF5){ref-type="table-fn"}R+R−R−/R+M−12 (8.8)760 (120)63M+1900 (400)2500 (180)1.3[^3][^4][^5] The HpyAXII R--M system effectively restricts incoming chromosomal DNA ---------------------------------------------------------------------- To investigate the role of the endonuclease R.HpyAXII in restricting incoming chromosomal DNA *in vivo*, we assessed transformation using donor genomic DNA harboring a kanamycin resistance marker (*aphA3*) at the 23S rDNA locus. This marker contains a GTAC site and is susceptible to cleavage by R.HpyAXII. As described for plasmid DNA, donor chromosomal DNA was isolated from bacteria encoding an active (M+) or inactive (M−) M.HpyAXII MTase. We determined if the endonuclease R.HpyAXII could restrict incoming chromosomal DNA by comparing transformation efficiency in NSH57 harboring either an active (R+) or inactive (R−) restriction endonuclease R.HpyAXII. When genomic DNA isolated from *H. pylori* lacking M.HpyAXII MTase activity (M−) was transformed into the bacteria harboring an active R.HpyAXII endonuclease (R+), a 240-fold decrease in transformation frequency was observed (R−/R+, [Table 3](#T3){ref-type="table"}). We also digested the same donor genomic DNA *in vitro* with RsaI prior to transformation, which lowered the transformation frequency further to undetectable levels ([Table 3](#T3){ref-type="table"}). We suggest that cleavage of the GTAC site in gene *aphA3* by the endonucleases RsaI and R.HpyAXII inactivates this marker and results in the subsequent decrease in transformation frequency. Overall, we demonstrated that active R.HpyAXII endonuclease effectively limits the incorporation of unmethylated exogenous homologous DNA into the *H. pylori* chromosome. Table 3.R.HpyAXII effectively restricts incoming genomic DNADonor DNA[^a^](#TF6){ref-type="table-fn"}Transformation frequency (\# transformants/recipient cell/ng × 10^−10^)[^b^](#TF7){ref-type="table-fn"}, mean (SEM)RatioRecipient strain[^c^](#TF8){ref-type="table-fn"}R +R−R−/R+M+18 (0.16)44 ([@B17])2.4M+ RsaI49 (9.3)95 ([@B30])1.9M−0.42 (0.26)100 ([@B11])240M− RsaI01.4 (0.60)inf [^d^](#TF9){ref-type="table-fn"}[^6][^7][^8][^9] The HpyAXII R--M system follows the selfish hypothesis ------------------------------------------------------ Kobayashi and colleagues suggested that type II R--M systems act as selfish genetic elements and cannot be easily replaced with a homologous stretch of DNA ([@B36]). This phenomenon, more commonly known as postsegregational killing, has been attributed to the gradual dilution of the modification and restriction enzymes in the descendants of the cell that lost the R--M system. Since there is asymmetry between the roles of the MTase and REase, newly replicated chromosomes will be inadequately protected by methylation and rendered susceptible to cleavage by the residual REase, leading to cell death. To determine whether the type II HpyAXII R--M system follows the selfish hypothesis, we deleted this chromosomal locus by allelic replacement from *H. pylori* strain NSH57 engineered to harbor an active (R+) or inactive (R−) R.HpyAXII endonuclease. We found that R− but not R+ recipient bacteria were easily transformed with donor NSH57 genomic DNA in which *hpyAXIIM/R* was replaced with a *catsacB* marker (strain NSH57 Δ*hpyAXIIM/R::catsacB*) ([Table 4](#T4){ref-type="table"}, Δ*hpyAXIIM/R*::*catsacB*). This 2100-fold decrease in transformation frequency seen for the R + recipient strain is independent of the digestion of GTAC sites in the donor DNA because they are fully protected by DNA methylation. We verified that the recipient strains were not generally defective at transforming DNA by showing allelic replacement at a different chromosomal region (ΔHP0368). In summary, we showed that chromosomal type II HpyAXII R--M system resists its replacement with an empty site in the presence of the active endonuclease R.HpyAXII, as described for other bacterial type II R--M systems ([@B38],[@B39]). Table 4.The HpyAXII R-M system follows the selfish hypothesisDonor DNATransformation frequency (\# transformants/recipient cell/ng DNA × 10^−10^)[^c^](#TF12){ref-type="table-fn"}, mean (SEM)RatioRecipient strain[^d^](#TF13){ref-type="table-fn"}R+R−R−/R+Δ*hpyAXIIM/R*::*catsacB*[^a^](#TF10){ref-type="table-fn"}0.15 (0.08)[^e^](#TF15){ref-type="table-fn"}320 ([@B21])2100Δ*hpyAXIIM*::*cat*[^b^](#TF11){ref-type="table-fn"}0.17 (0.17)[^f^](#TF15){ref-type="table-fn"}1100 (350)6500ΔHP0368::*cat*[^b^](#TF11){ref-type="table-fn"}310 (9.2)180 ([@B38])0.58[^10][^11][^12][^13][^14][^15] An active R.HpyAXII REase can only exist in the presence of its active DNA MTase partner ---------------------------------------------------------------------------------------- We predicted that bacteria harboring a functional REase must also encode an active cognate DNA MTase to protect the genome from digestion. The R + M− phenotype should therefore be lethal, a condition especially relevant for the HpyAXII R-M system since many of the cognate sites are present within the rRNA genes ([Table 1](#T1){ref-type="table"}). Thus we deleted *hpyAXIIM* by allelic replacement using the Δ*hpyAXIIM*::*cat* PCR construct in bacteria harboring active (R+) or inactive (R−) endonuclease R.HpyAXII ([Supplementary Figure S3](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)). We observed a dramatic reduction in transformation efficiency (6500-fold) for the R + bacteria ([Table 4](#T4){ref-type="table"}). In comparison, allelic replacement at a different chromosomal region (ΔHP0368) was carried out at a similar efficiency in R + and R- bacteria ([Table 4](#T4){ref-type="table"}). Importantly, the observed decrease in transformation efficiency is independent of the cleavage of incoming Δ*hpyAXIIM*::*cat* donor DNA by the endonuclease R.HpyAXII since this fragment is devoid of GTAC sites. Rather, recombinants for the R+ bacteria probably died from double-stranded breaks in their chromosomal DNA. We were intrigued by the rare transformants obtained when gene *hpyAXIIM* was deleted in the R+ bacteria because it suggests that the R+M− phenotype is occasionally viable. We investigated these clones further and found evidence of gene amplification and adaptive mutations at the M.HpyAXII/R.HpyAXII locus. From three independent transformations, we analyzed a total of 16 clones; seven displayed evidence of gene amplification and nine showed adaptive mutations. For gene amplification, *hpyAXIIM* was present in both a wild-type and a mutated form at the same locus ([Supplementary Figure S3](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)), overall resulting in the phenotype R+ M+. This diploidy for *hpyAXIIM* was unstable and the mutant form of the gene was generally lost after several passages *in vitro* (data not shown). In other clones, point mutations were found in the promoter region of gene *hpyAXIIR*, specifically in the ribosome binding sequence and in the start codon of the gene ([Figure 3](#F3){ref-type="fig"}). In all cases, these mutations likely prevent effective translation of the endonuclease R.HpyAXII; the overall phenotype of these clones therefore became R−M−. We conclude that *H. pylori* bacteria only harbor an active R.HpyAXII endonuclease in the presence of an active M.HpyAXII MTase. Figure 3.Deletion of *hpyAXIIM* from a *H. pylori* strain harboring an active endonuclease R.HpyAXII yielded rare transformants that display adaptive mutations in the promoter region of *hpyAXIIR*. Gene *hpyAXIIR* was sequenced in nine surviving recombinants obtained following *hpyAXIIM* deletion. When compared to wild-type, single base deletions and substitutions (highlighted in gray) were detected in the transformants in both the ribosomal binding site (RBS) and start codon (START) of *hpyAXIIR*. The adenine MTase M.HpyAXII is highly conserved among *H. pylori* strains ------------------------------------------------------------------------- *Helicobacter pylori* R--M systems are remarkably heterogeneous among strains. Some are present in a fraction of strains, absent in others, or inactivated by deletion or frameshift mutations. It has been estimated that less than one-third of *H. pylori* R--M systems are fully active ([@B6]). We were interested in determining whether M.HpyAXII is present and active in a panel of *H. pylori* clinical isolates. We found that the HpyAXII R--M system is well conserved as we amplified this locus from all 50 pediatric clinical isolates isolated from 47 patients (S. Talarico, J. Fero, D.T. Thompson, J. Guarner, S. Czinn. B.D. Gold, N.R. Salama, personal communication) though its size was reduced in four (8%) strains (data not shown). To assess M.HpyAXII MTase activity for the clinical isolates, we digested each strain\'s genomic DNA with the REase RsaI, which only cleaves unmethylated GTAC sites. Of the 50 clinical isolates DNA, only four strains were digested with RsaI, all of which displayed a smaller amplified product for the HpyAXII R--M system (data not shown). M.HpyAXII activity is therefore remarkably conserved among *H. pylori* strains (92% active as tested). To determine how M.HpyAXII was inactivated in the four *H. pylori* strains lacking DNA MTase activity, we sequenced the HpyAXII R--M system. In all strains, most of *hpyAXIIM* and *hpyAXIIR* coding region was substituted by a gene in reverse orientation ([Figure 4](#F4){ref-type="fig"}). This replacing gene, that we name *hrgC* (HpyAXII replacing gene C), shows strong homology to *Helicobacter acinonychis sheeba* Hac_1467 (80% nucleotide identity). Hac_1467 is present at a different chromosomal region in this species (557 kb away from the HpyAXII locus) and encodes a 94 amino acid protein of unknown function. In the four clinical isolates where gene replacement occurred, *hrgC* encodes a protein of 94- or 128-amino acids. A search for orthologs of Hac_1467 at the *H. acinonychis* locus using a PCR approach was negative for all 50 clinical isolates and only positive for *H. pylori* strain NSH57. Surprisingly, in both *H. acinonychis sheeba* and *H. pylori* NSH57, Hac_1467 is preceded by a 165 bp DNA fragment (Hac_1466) that shows high homology to the 5′-end of *hpyAXIIM* (89% sequence identity, [Figure 4](#F4){ref-type="fig"}), suggesting that some recombination event took place at this locus. In summary, we demonstrated that the activity of the DNA MTase M.HpyAXII is highly conserved among *H. pylori* strains but can be disrupted by insertion of the alternate gene *hrgC* at the same locus in several unrelated strains. Figure 4.M.HpyAXII MTase activity is occasionally disrupted by insertion of the alternate gene *hrgC*. The HpyAXII R--M system was sequenced in the *H. pylori* clinical isolates where M.HpyAXII was found inactivated (M−). In all M− strains, most of the HpyAXII locus was replaced with alternate gene *hrgC* that shows strong homology to Hac_1467 (80% nucleotide identity) from *Helicobacter acinonychis sheeba*. Depending on the strain analyzed, gene *hrgC* is either 285- or 387-bp long. The REase R.HpyAXII is poorly conserved among *H. pylori* strains ----------------------------------------------------------------- The conservation of M.HpyAXII MTase activity in *H. pylori* isolates led us to evaluate R.HpyAXII activity in these same isolates. We developed a genetic assay to assess R.HpyAXII endonuclease activity based on the previous finding that the MTase M.HpyAXII cannot be deleted in the presence of an active REase. Since *H. pylori* strains vary in their ability to be transformed by exogenous DNA, we chose to engineer strain NSH57 to contain the HpyAXII R-M system from the different clinical isolates using allelic replacement and a knockin approach (Materials and methods section). We transformed the resulting clones with the Δ*hpyAXIIM*::*cat* donor DNA to delete gene *hpyAXIIM*. When a large number of transformants were recovered, we deduced that R.HpyAXII from that particular strain lost endonuclease activity. In contrast, when few or no transformants were obtained, we concluded that R.HpyAXII must be active because of the lethality of the R + M− phenotype. The DNA fragment ΔHP0368 was used as transformation control. We first evaluated R.HpyAXII activity in the NSH57 clones engineered to contain the HpyAXII R-M system from *H. pylori* strains NSH57, J99, NSH79 and HPAG1. As expected from our genomic and biochemical results ([Figures 1](#F1){ref-type="fig"}B and [2](#F2){ref-type="fig"}), only the clone harboring the HpyAXII R--M system from strain HPAG1 showed a dramatic reduction in transformation efficiency when gene *hpyAXIIM* was deleted ([Supplementary Figure S4](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)). In contrast, clones harboring HpyAXII from strain NSH57, NSH79 and J99 yielded a large number of transformants, confirming that the endonuclease R.HpyAXII is inactive in these strains. This result therefore validates the use of our genetic assay to investigate R.HpyAXII endonuclease activity. We constructed NSH57 clones harboring the HpyAXII R-M system from 37 clinical isolates and found that R.HpyAXII was only active in seven clones (18.9%) based on the number of transformants recovered. All strains could successfully be transformed with the ΔHP0368 PCR product, ruling out a general defect in transformation. We examined the nature of mutations that inactivated R.HpyAXII in the 30 *H. pylori* isolates by sequencing gene *hpyAXIIR*: nine strains (30%) contain a large deletion (39AA) similar to the one found in strain NSH57 ([Figure 1](#F1){ref-type="fig"}B), seven strains (23%) harbor nonsense mutations that result in a truncated protein, two strains (7%) have both the deletion and nonsense mutations, and 12 strains (40%) contain single nucleotide polymorphisms (SNPs) in the coding region of gene *hpyAXIIR*. For four strains, we confirmed that the *hpyAXIIR* sequence was identical in the engineered strain and in the original isolate, ruling out the possibility that mutations were introduced during the genetic manipulations. To analyze the inactivating SNPs in more details, we aligned the protein sequences from the 12 inactive and seven active R.HpyAXII enzymes with that of *H. pylori* strain HPAG1, shown to be active. We identified between two and five amino acid substitutions per strain that may inactivate R.HpyAXII function, resulting in a total of 31 distinct coding SNPs. The nature and frequency of these substitutions are described in [Figure 5](#F5){ref-type="fig"}A and the SNPs for each strain are described in [Supplementary Table S3](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1). These coding SNPs were mapped on the primary protein sequence of R.HpyAXII ([Figure 5](#F5){ref-type="fig"}B) as well as on the three-dimensional model based on R.PabI crystal structure ([Figure 5](#F5){ref-type="fig"}C) ([@B40]). Out of these 31 SNPs, two (\#5 and \#18) overlap with residues previously shown to be required for R.PabI activity ([@B40]), and seven are found in multiple *H. pylori* strains ([Figure 5](#F5){ref-type="fig"}A). Several structural motifs (β3, α3, β6, β8, β10 and α4 based on R.PabI) contain a high density of SNPs and may be crucial for R.HpyAXII endonuclease activity. Figure 5.Protein sequence analysis of 12 inactive R.HpyAXII enzymes reveal 31 distinct coding SNPs. (A) Comparison of R.HpyAXII protein sequences in 12 *H. pylori* strains harboring inactive enzyme and in seven strains harboring active enzyme with that from strain HPAG1 identified 31 coding SNPs, enumerated \#1 through \#31 with the conservation and frequency of each substitution indicated. (C) - conserved, (S) - semiconserved, (-) - unrelated. Changes highlighted in gray were found in multiple strains and changes highlighted in purple were previously shown to be required for R.PabI activity ([@B40]). (**B**) HPAG1 R.HpyAXII and R.PabI protein sequences were aligned and the position of each SNP highlighted. Red, potentially inactivating SNPs numbered \#1 through \#31; cyan, previously shown to be required for R.PabI activity and target the predicted DNA-binding domain; purple, coding SNPs in R.HpyAXII also required for R.PabI activity. (\*) - identical residues, (:) - conserved substitution, and (.) semi-conserved substitution. (**C**) Coding SNPs were mapped on the three-dimensional model generated for R.HpyAXII based on the R.PabI crystal structure using the same color code used in (B). *H. pylori* M.HpyAXII MTase activity is not required for establishing infection in mice --------------------------------------------------------------------------------------- The remarkable preservation of M.HpyAXII activity in *H. pylori* strains and the intriguing distribution of chromosomal GTAC sites led us to investigate whether this DNA MTase confers a selective advantage to *H. pylori* during infection. We were also interested in determining whether M.HpyAXII has a role during infection that is independent of its DNA MTase activity. For this reason, we infected mice with *H. pylori* NSH57 deletion mutant (Δ*hpyAXIIM*::*cat*) and with the catalytically inactive mutant (*hpyAXIIM*^N87A^), which MTase can presumably still bind DNA but not methylate it. Mouse stomachs were harvested after one week of infection and viable bacteria were recovered and enumerated to calculate the competitive index for each infection \[colony forming units (CFU) mutant bacteria/CFU wild-type bacteria\] (Materials and methods section). When mice were infected with NSH57Δ*hpyAXIIM*::*cat* mutant and wild-type bacteria, equal number of bacteria were recovered (*n* = 9, [Figure 6](#F6){ref-type="fig"} left) indicating that they could establish infection at a similar efficiency. M.HpyAXII protein expression is therefore not required for establishing infection in *H. pylori* strain NSH57. We also infected mice in competition with the catalytically inactive mutant *hpyAXII*^N87A^ and the deletion mutant Δ*hpyAXIIM*::*cat*. Both strains infected mice similarly (*n* = 9, [Figure 6](#F6){ref-type="fig"} right) indicating that M.HpyAXII does not have a role during establishment of infection that is independent of its DNA MTase activity. Figure 6.M.HpyAXII MTase activity is not required by *H. pylori* for establishing infection in a mouse infection model. Mice were infected in 1:1 competition with the indicated *H. pylori* strains and the competitive index (CI) determined after one week of infection. The CI was calculated by dividing colony forming units (CFU) recovered of null mutant bacteria over CFU wild-type or point mutant bacteria and corrected by dividing the actual input ratio enumerated from plating the inoculums. Left, mice (*n* = 9) were infected with *H. pylori* NSH57 wild-type and an isogenic null mutant *ΔhpyAXIIM*::*cat*. Both strains infected mice at a similar efficiency (geometric mean CI slightly above one). Right, mice (*n* = 9) were infected with the NSH57*ΔhpyAXIIM*::*cat* mutant and the catalytically inactive mutant (*hpyAXIIM*^N87A^) constructed in strain NSH57. DISCUSSION ========== *Helicobacter pylori* naturally takes up exogenous DNA, a condition thought to promote genetic diversification by spreading new alleles in the population. However, genetic exchange is limited by the large number and heterogeneity of *H. pylori* R--M systems ([@B6]). The contribution of individual R--M systems in restricting incoming DNA remains for the most part undetermined since only a few of these systems have individually been tested in *H. pylori* ([@B37],[@B41]). In addition, it is possible that R--M systems carry out other biological roles. In our study, we have biochemically characterized a novel *H. pylori* type II R--M system, M.HpyAXII/R.HpyAXII, and showed that it targets GTAC sites thus confirming prior predictions ([@B35]). The endonuclease R.HpyAXII effectively restricted both unmethylated plasmid (60-fold) and genomic (240-fold) DNA ([Tables 2](#T2){ref-type="table"} and [3](#T3){ref-type="table"}). Our results agree with previous reports documenting effective restriction of plasmid DNA by R.HpyAIII (encoded by HP0091, GATC) ([@B37]), and of chromosomal DNA by R.HpyAII (encoded by HP1366, GAAGA) ([@B41]). Since R--M systems are highly polymorphic in *H. pylori*, we analyzed the conservation of both M.HpyAXII MTase and R.HpyAXII endonuclease activities in a panel of clinical isolates. We found a striking asymmetry between the highly conserved MTase activity (92% active, *n* = 50) and that of the REase (18.9% active, *n* = 37). In fact, our data indicate that M.HpyAXII is the third most highly conserved adenine MTase in *H. pylori*, preceded only by M.HpyAI (CATG, 100% conserved) and M.HpyAIII (GATC, 97% conserved) ([@B42],[@B43]). Other studies have suggested that MTase activities are generally selected for in *H. pylori* ([@B6],[@B29],[@B44]) but how DNA methylation benefits the organism is unknown. To begin to probe how M.HpyAXII affects *H. pylori* biology, we generated a null allele in gene *hpyAXIIM* in mouse-adapted strain NSH57 either by deletion or by targeted mutation of the catalytic site of the enzyme (*hpyAXIIM*^N87A^). Mouse infection with these strains indicated that M.HpyAXII expression is not required by *H. pylori* for the establishment of infection ([Figure 6](#F6){ref-type="fig"}) in contrast to previous work ([@B19]). As this study did not complement the mutant phenotype, it is possible that second site mutations or polar effects accounted for the defect observed. Further experiments are needed to determine if M.HpyAXII activity is important during persistent infection and to elucidate how GTAC methylation provides a selective advantage in *H. pylori*. It was proposed that the maintenance of an active MTase allows reactivation of a given R--M system through recombination with the genomic DNA of a strain that encodes an active REase. However, the probability of this event must be relatively low given that R.HpyAXII is active in a small number of strains. It was also postulated that 'orphan' MTases are conserved because they act as a 'molecular vaccine' against the parasitism of R--M systems. This hypothesis was based on the finding that Dcm in *E. coli* can alleviate postsegregational killing induced by the EcoRII R--M complex that recognizes the same sequence as Dcm ([@B45]). This also seems unlikely because no R--M system that acts on the same site as HpyAXII has been identified in *H. pylori*. DNA methylation may alternatively be selected for in *H. pylori* because it confers immunity from the action of the cognate REase and therefore increases the chances that an entire gene is successfully propagated in a population. However, the finding that the average size of recombined fragment is unusually small (417 bp) in *H. pylori* as compared to other bacteria indicates that incoming DNA is generally susceptible to cleavage by REases ([@B46]). Another important role of DNA methylation is to modulate the interaction between proteins and DNA as demonstrated for the stand-alone adenine MTase Dam in α- and γ-Proteobacteria ([@B14],[@B15],[@B47]). DNA MTases involved in R--M systems that are not coupled to an active REase may have evolved similar regulatory functions since they are no longer under the pressure to act on all chromosomal sites and may therefore preferentially methylate sequences required for transcription. The genome-wide analysis of conserved GTAC sites identified genes of various functional classes including several genes of the cag pathogenicity island but it is unknown whether their expression is affected by M.HpyAXII methylation. Although GTAC sites are scarce in the *H. pylori* chromosome, they are present at high frequency in the 23S and 16S rRNA genes. Our preliminary experiments showed no effect of M.HpyAXII methylation on 23S rRNA transcripts levels or on *in vitro* growth of the bacteria (data not shown), arguing against a role for GTAC methylation in *H. pylori* ribosomal biogenesis. It is possible that ribosomal GTAC sites are preserved because they are crucial for the folding of the RNA into functional secondary structures in Helicobacter species and that methylation of these sites does not have any biological role. In agreement with this hypothesis, the analysis of 23S rRNA sequences in 55 Helicobacter strains representing 41 taxa ([@B48]) shows conservation of most GTAC sites even though many of these species probably lack a M.HpyAXII enzyme. Alternatively, ribosomal GTAC sites may not have been erased from these chromosomal regions because they evolve at a different rate than the rest of the genome; these elements are duplicated in *H. pylori* and are subjected to homogenization processes such as gene conversion ([@B49]). Overall, the significance of ribosomal GTAC sites in *H. pylori* remains unsolved but echoes a similar anomaly in site distribution with the tetramer CTAG that is very rare in *E. coli* and in other proteobacterial genomes and over-represented in rRNA genes ([@B50],[@B51]). The comparison of tetranucleotide combinations in 27 representative microbial genomes revealed that ACGT, GTAC and TCGA are strongly underrepresented in both coding and noncoding DNA in *H. pylori* ([@B52]). A significant correlation between the avoidance of palindromic words and type II R--M systems was suggested ([@B53]) presumably because these systems exert significant pressure on an organism when restriction is intact but methylation is incomplete. However, the highly conserved *H. pylori* R--M systems M.HpyAI/*iceA* (CATG) or M.HpyAIII/R.HpyAIII (GATC) target sites are not underrepresented in the *H. pylori* genome. Since cognate site avoidance is probably dependent on the timing of acquisition of a given R--M system during evolution, the HpyAXII R--M system must have been acquired a long time ago, consistent with the finding that this system is present in all *H. pylori* isolates analyzed. Interestingly, GTAC sites are also scarce in the *Helicobacter hepaticus* genome even though it does not encode an M.HpyAXII/R.HpyAXII ortholog. This can either be explained by the recent loss of this system or by the existence of a different R--M system that acts on GTAC sites in *H. hepaticus*. Our study of the conservation of M.HpyAXII MTase activity uncovered the occasional replacement of the HpyAXII R-M system with an alternate gene that we re-annotate as *hrgC* (HpyAXII replacing gene C). Other *H. pylori* R--M systems encoding the two most highly conserved MTases M.HpyAI and M.HpyAIII are similarly replaced with genes of unknown function. In the HpyAIII R--M system, gene *hrgA* inactivated the REase R.HpyAIII in 33% of the 208 strains analyzed but rarely inactivated M.HpyAIII function ([@B54]). *hrgA* encodes a 370 amino acid protein of unknown function and this gene was associated with gastric cancer in *H. pylori* isolates from Asian patients but not among Western strains ([@B55]). In the HpyAI R--M system, the REase encoded by *iceA1* was replaced with *iceA2* in 44% of the strains analyzed ([@B56]). *iceA2* (renamed *hrgB*) encodes a polymorphic protein of unknown function ranging from 24 to 59 amino acid long depending on the strain studied, and epidemiological studies have correlated the presence of gene *iceA1* in *H. pylori* strains with the incidence of peptidic ulcers disease ([@B57]). In our study, we showed that similarly to *hrgA* and *hrgB*, *hrgC* encodes a protein of unknown function but its origin could be traced to a different locus in *H. acinonychis sheeba* and *H. pylori* strain NSH57 (G27). Unlike *hrgA* and *hrgB*, *hrgC* replacement always compromised both the MTase and REase activities in our analysis of 37 clinical isolates. Further work will define whether *hrgC* has any role in *H. pylori* pathogenicity. As predicted for a type II R--M system, we showed that deletion of gene *hpyAXIIM* is lethal in the presence of an active R.HpyAXII endonuclease. The lethal phenotype R+M− can be rescued by adaptive mutations, in the form of gene amplification of *hpyAXIIM* and null mutations in the promoter region of *hpyAXIIR*. This result is reminiscent of extensive research describing stress-induced mutations in *E. coli* with the Lac assay system ([@B58]). Based on these findings, we suggest that these adaptive mutations preexisted in the *H. pylori* population and were selected for as a result of *hpyAXIIM* deletion. Tandem amplification was previously documented for R--M systems, as when the entire BamHI R--M system was deleted from *Bacillus subtilis* ([@B38]). In another study, large-scale genomic rearrangements were demonstrated when the PaeR71 R--M system was deleted from *E. coli* ([@B39]). These rearrangements involved recombination between copies of the transposon IS3 and were proposed to have resulted from multiple rounds of unequal crossing-over or rolling circle amplification. Our study of the deletion of the MTase gene in the HpyAXII R-M system is the first to demonstrate the occurrence of compensatory mutations in the promoter of the respective REase gene. Orthologs of M.HpyAXII generally show poor sequence homology except for one gene of unknown function from *Campylobacter upsaliensis* RM3195 (CUP1644) that shows 43% identity with M.HpyAXII. Other adenine MTase that target GTAC sites such as M. PabI from *Pyroccoccus abyssi* and M.CviQI from Chlorella virus only show 14.6% and 17.8% protein identity, respectively. M.RsaI (7.9% protein identity) from *Rhodopseudomonas sphaeroides* and M.MjaV from *Methanococcus janaschii* (12.7% protein identity) act on the same sequence but methylates cytosines (m4C). GTAC sites are strongly avoided from the genomes of *R. sphaeroides* and *M. jannashi* but not from *P. abyssi*, suggesting that the PabI R--M system invaded this organism recently as discussed previously ([@B35],[@B59]). The crystal structure of the endonuclease R.PabI was recently solved and unveiled a novel protein fold termed 'half-pipe' ([@B40]). Although the two isochizomers R.PabI and R.HpyAXII show relatively weak sequence identity (25.4%), several conserved motifs are shared between the two proteins ([Figure 5](#F5){ref-type="fig"}B). The R.HpyAXII polypeptide could be threaded with high confidence onto the tertiary structure of R.PabI (PHYRE, *E*-value 3e-26, [Figure 5](#F5){ref-type="fig"}C) suggesting that R.HpyAXII folds into a similar half-pipe structure. Among the thousands of confirmed and hypothetical REase enzymes identified, Orlowski and Bujnicki predicted that only eight present the half-pipe fold ([@B60]). R.HpyAXII therefore constitutes an excellent candidate for refined biochemical analyses that will enrich our understanding of this new class of enzymes. SUPPLEMENTARY DATA ================== [Supplementary Data](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1) are available at NAR Online. FUNDING ======= National Institutes of Health (AI054423 and DK53708 to N.R.S., AI55396 to O.H.). Funding for open access charges: National Institutes of Health (AI054423). *Conflict of interest statement*. The project\'s contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH. Supplementary Material ====================== ###### \[Supplementary Data\] We thank Marion Dorer for critical reading of the article, Laura Sycuro for generating the *catsacB* cassette, New England Biolabs for providing the m6A antibodies and Barry Stoddard for helpful discussions. [^1]: ^a^Based on 26695 annotation ([@B61]). [^2]: ^b^The number of conserved sites is given when higher than one. The exact position of the site is given only when within 200bp from the start codon of a gene. [^3]: ^a^Donor plasmid pTM113-*cat* contains a total of five GTAC sites and was constructed by substituting *cat* for *aphA3* in pTM113 ([Supplementary Table S3](http://nar.oxfordjournals.org/cgi/content/full/gkn718/DC1)). pTM113-*cat* was isolated from *H. pylori* strain NSH57 wild-type (M+) or NSH57*hpyAXIIM*^N87A^ (M−). A total of 3.3 ng of plasmid DNA was used for each transformation. [^4]: ^b^Transformation frequency was calculated by dividing the number of transformants recovered by the total number of recipient bacteria and was based on the average of three replicates. [^5]: ^c^Strain NSH57*hpyAXII*~HPAG1~ (R+) encodes an active R.HpyAXII and strain NSH57*hpyAXIIM/R*~HPAG1~ Δ*hpyAXIIR*::*aphA3* (R−) lacks this enzyme. [^6]: ^a^Donor genomic DNA was constructed by inserting the *aphA3* cassette at position 2586bp (from start codon) in one of the two copies of 23S rDNA genes. One GTAC site is present in *aphA3* at position \#94 bp and three flanking GTAC sites are found in close proximity to the marker at positions \#2527, \#2660 and \#2745**.** Chromosomal DNA was isolated from *H. pylori* strain NSH57 wild-type (M+) or NSH57Δ*hpyAXIIM::cat* (M−), and predigested or not with RsaI. A total of 10 ng genomic DNA per tranformation was used for M− and 7.9 ng for M+. [^7]: ^b^Transformation frequency was based on the average of three replicates. [^8]: ^c^Strain NSH57*hpyAXIIM/R*~HPAG1~ (R+) encodes an active R.HpyAXII and strain NSH57*hpyAXIIM/R*~NSH57~ (R−) encodes an inactive enzyme. [^9]: ^d^Ratio is infinite because no transformants were recovered for R+ recipient strain [^10]: ^a^NSH57 wild-type genomic DNA was constructed by replacing the entire HpyAXII R-M system with the *catsacB* marker. 500ng genomic DNA per transformation was used. [^11]: ^b^A PCR product was engineered to disrupt genes *hpyAXIIM* or HP0368. The 5′ and 3′ homologous ends of the respective gene was fused to the antibiotic resistance cassette and transformed to generate a null allele by allelic replacement. A 150ng DNA per transformation was used for Δ*hpyAXIIM*::*cat* and ΔHP0368::*cat*. [^12]: ^c^Transformation efficiency was based on the average of three replicates. [^13]: ^d^As in [Table 2](#T2){ref-type="table"}. [^14]: ^e^A total of two clones was recovered. [^15]: ^f^A total of five clones was recovered.

3.03125

3

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Q: Class Inheritance and Casting So I was given this code in a folder of bits and pieces that were to be for a project which has since halted development. However, being new to Java there are several questions I have (and I'm aware the code does not compile, but that works into one of my questions). interface Executable { public int execute (Object o); } public class Biv implements Executable { public int execute (String s) { System.out.println (s); return s.length(); } public static void main (String[] args) { Executable e = new Biv(); System.out.println( e.execute ("Hello World!")); } } 1) My first question is to do with the variable e. It is declared with the Executable object type, however I don't understand why it can then be instantiated with a new Biv object. What is going on here, what does it mean? 2) The error is in the execute method within the Biv class. This seems to be because it expects an object rather than a String. However, can you not replace a Object with a String because String is a subclass of Object? I could understand if you replaced String with Object it would have an error (I think) but not how it is currently done. A: I don't understand why it can then be instantiated with a new Biv object Because Biv implements Executable, so any instance of Biv is also an instance of Executable. The error is in the execute method within the Biv class Yes it is, it [Biv] does not implement execute(Object). The method execute(String) is just a different method that happen to have the same name, since they don't have the same signature. Any class that implements the interface Executable must override the method execute(Object). There is no co-variance of arguments in java for overriding methods, because it will be unsafe. What if you invoked e.execute(new Object())? [where e is referencing a Biv object] Biv will not know what to do with it.

3

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Inside every living cell are molecule-building factories called ribosomes. These tiny machines read blueprints of genetic information and fabricate the molecules that make up all life. They are hugely important to genetic engineers and researchers, because controlling ribosomes could be the way to synthesize the custom-made biological nano-machines of the future—ones that could make anything from therapeutic human antibodies to the next generation of unfathomably complex super-materials. There's a problem: Engineering a ribosome to do interesting tricks often means paralyzing and killing its parent cell. But today, a team of biologists and biological engineers at Northwestern University and the University of Illinois have made a fascinating breakthrough that could help scientists get around this roadblock. As they report in a new study in the journal Nature, the scientists have created unique, experimental ribosomes they're calling Ribo-T that are the first ever to passively co-exist with a living cell's natural ribosomes. It means that for the first time, researchers will be able to tinker with ribosomes in living organisms, such as bacteria, without worrying about killing the lifeforms they're studying. "You can think of it like this: Imagine you only have one family car and you want to start modifying it, say, putting a truck bed in," says Alexander Mankin, a biologist with the team at the University of Illinois. "With each modification, you risk breaking down important processes, like losing the back seat your kids need. This is the same with these ribosomes. But here, [having Ribo-T] is a bit like having two cars, instead of one." So you can modify Ribo-T in any way you want without worrying about destroying the whole setup, he says. The genetic lasso What makes ribosomes so hard to work with is their fundamentally weird nature. Here's an oversimplification of the strange setup: In all living cells, ribosomes are broken up into two independently floating parts. There's a smaller "reader" half of a ribosome, which attaches to a strip of genetic data, and a larger half that assembles the molecules. Each cell is a sea of ribosomes halves. Those halves randomly join together to read and create a molecule, then split up and promiscuously recouple with totally different halves. Based on what we know about cell biology, this really shouldn't have worked. According to Mankin, that two-parted nature has made genetically engineering these molecules machines almost impossible. You either genetically engineer the whole sea, or nothing at all. But Mankin and his fellow scientists had an idea, one that totally went against what scientists thought they understood about ribosomes. Why not just tie the two halves of certain ribosomes together indefinitely? Based on what we know about cell biology, this really shouldn't have worked. The reason is that the two ribosome halves need to move around relative to each other as they built molecules, which a tether might prevent. Researchers also didn't know how such a tied-together ribosome would find the strips of genetic data blueprints it reads. For the most part, it didn't work. Mankin and his colleagues tried to tie the ribosome halves together tethers of basically nonsense sticky RNA. They tried 91 different combinations, and most of them failed. A few of them worked, albeit it very poorly. But here's where the team did something really clever: They let a cutthroat competition decide which tether was best. By joining the RNA of the large and small ribosomal subunits into a unique chimaeric molecule, it was possible to engineer functional ribosome with tethered ribosomal subunits (Ribo-T) Eric Carlson The researchers were thinking that the length of the tethers might impact how well the combined ribosomes were able to function, since the ribosome halves need to shift around without breaking their connection. So Mankin and his team genetically engineered a handful of bacteria with tied-together ribosomes, each with different tether lengths. Then the scientists let them compete on a petri dish with limited food for two days to see which bacteria out-competed the rest. "This way the cells told us themselves what was the best ribosome tether design in the smorgasbord of options we offered," he says. In the end, bacteria with two sticky tethers 8 and 9 RNA nucleotides long was the champion. Having found the optimal length, the scientists did one last round of bacterial gladiator battle to se whether—with enough time—some bacteria might spontaneously evolve some trait that would make the combined ribosomes more efficient. "After several dozens of generations, a bacteria did," Mankin says, and it dominated a different petri dish with more gusto than any other strain. (Exactly why this random mutation allowed a bacterial with a combined ribosome to grow faster is still a mystery, he says.) Scaffolds for the science of the future "The answers to these questions will illuminate the basic mechanisms of molecule creation." Finally, Mankin and his team had created a combined and tethered ribosome that works surprisingly well: Ribo-T. A bacterial cell using only Ribo-T ribosomes will grow normally, but at about 45 percent the speed of a non-engineered cell. Joseph Puglisi, a biologist at Stanford University who was not involved with the project, says that figure is actually damned impressive. In an essay accompanying the Nature paper, Puglisi confirms that Ribo-T, while a bit slower, can create any of the molecules a normal ribosome can make. That makes Ribo-T—which can be genetically created to appear alongside a population of normal, halved ribosomes—the perfect scaffold for a new wave of genetic engineering experiments. Better still, Puglisi says, because we now have the first platform where we can test and tinker with truly delicate and crucial ribosomal features (without worrying about killing our experiment), Ribo-T may offer new insights into the mysterious inner-workings of the ribosome—which, as Mankin admits, is still poorly understood. We can now ask basic questions like why ribosomes seem unable to create certain types of molecules. "The answers to these questions will illuminate the basic mechanisms [of molecule creation] and will probably cause surprise," Puglisi says. "Armed with this knowledge, thoughtful engineers will continue to tinker with the ribosome. This content is created and maintained by a third party, and imported onto this page to help users provide their email addresses. You may be able to find more information about this and similar content at piano.io

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[Diet and lifesyle of a cohort of primary school children]. The obesity is the disease of the new millennium, because it affects about 300 million people in the world, and especially it has a high prevalence in children. Obesity is a significant risk factor for cardiovascular disease, diabetes mellitus type II, hypertension, problems of adaptation and relationship with other, lower self-esteem and depression. The objective of our study is to identify children at risk of overweight/obesity in order to primary prevention. We have organized meetings with children, families and school's members where we discussed the results of our investigation about the importance of healthy diet and lifestyle. The study was carried out on 545 children (282F, 263M), age 6.-10 years, of two primary schools in Catanzaro, from 2008 to 2010. The valuation parameters were: gender, age, weight, height, blood pressure and waist circumference. To children were also administered a questionnaire about dietary habits and lifestyle. Fisher's test. We had that 62% of children was normal weight, 27% overweight, 11% obese. A particularly relevant datum is that the percentage of overweight-obese boys of 8 and 9 years old was higher (56%) than that of normal weight. We found cases of hypertension only in obese children. 98% of obese, 80% of overweight and 24% of normal weight children had a high waist circumference. We did not find differences in food quality among normal weight and overweight/obese children. Instead, we found significant differences in behavior between children: 90% of obese, 64% of overweight and 53% of normal weight children passed more than 2 hours in the afternoon watching television, playing computer and video games. 70% of normal weight, 82% of overweight and 95% of obese children practiced physical activity. Our study shows a alarming fact about the increase of the obesity in children. In particular the most important problem is that this condition could predispose to cardio-metabolic, endocrine, respiratory, musculoskeletal and psychological consequence. So it is important that everybody who lives with children, especially parents and school's members, educates children to have healthy lifestyles. These attentions may slow the worryng epidemic of obesity.

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Look at the science behind the prevention method To find a cancer prevention method with a proven track record, look at how the method was tested. The way tests are set up can affect the outcome, and sometimes can make it look like a method or substance prevents cancer when it really doesn’t. Pre-clinical tests Studies in cells (laboratory studies) Scientists usually start by testing a new prevention method or treatment on cells in a dish in the lab, to find out if it has any effect there. They may treat cells with a known cancer-causing agent and then add the compound they’re testing to see if it stops pre-cancerous changes in the cells. If it doesn’t, they may change the formula or use different types of cells to try it again. Sometimes studies like this show some effect on the cells, and they’re published. News broadcasters may then treat the study as proof that a cancer prevention method works. But just because a compound stops abnormal cell growth when it’s added to cells in a lab dish does not mean that it will work in the human body. This means that if you're looking at a report of a research study – even one that says a treatment “stops the growth of cancer cells” – you may notice that there’s no mention of people. Some of these lab studies use human cancer cells, but others use cancer cells from animals. (Either way, studies done on cells alone are called in vitro studies.) At this point, anything that stops cancer cells may sound like good news. But there are many compounds that can keep cancer cells from growing in a lab dish that don’t work or aren’t safe in people. Some reasons a treatment might not work for people is that the substance also hurts or kills normal cells, or because the body can’t absorb it and get it to the place where it’s needed to stop cancer. Sometimes, even if the substance can be absorbed, can reach all the body tissues, and doesn’t harm normal cells, the amount of the substance that gets to the tissues isn’t enough to stop the cancer cells. There are many hurdles between lab studies and human ones. Studies in animals If the researchers find the effect they want in cells in a dish, they may move on to animal tests. This can help them find out if the substance can be absorbed from the stomach or intestine, and learn how it’s distributed in the animal’s body. They may look for good and bad effects. Because some of these reports are published, you may also hear about them on the news. These are called in vivo studies. This means that they were studied in living creatures. If the study was done in animals, good outcomes may sound promising. But methods that work in animals don’t always work when they are tested on people. Animal studies often help scientists know which drugs may be toxic to people, and which may have unexpected effects. Sometimes a drug or food supplement turns out to do almost the exact same things in people as animals, but many don’t work for one or the other. And as any veterinarian can tell you, some foods and drugs that are safe for animals can hurt people, and some foods and drugs that are safe for people can hurt animals. So while animal tests can give researchers certain types of valuable information, they still may not show how the compound will affect people. News stories on lab and animal studies can mislead In both lab studies and animal studies, the research report may be published. Usually, the researcher’s own report makes it clear that more studies need to be done to see if the substance makes a difference in people. But if a news group picks up the story and publishes it, they may not mention how the study was done or that more study is needed. Often the headlines, and sometimes even the full story, do not clearly say what kind of study was done. Sometimes the news reports on this very early research may make it sound like the method will work in people, which can lead to confusion. This is why it helps to look at the whole printed story, and then see if you can find out more about the details of the research. Always keep in mind that there’s a huge difference between positive results in lab or animal studies and good results in human studies. Select A Hope Lodge Please share your thoughts about your cancer.org website experience. If you need immediate cancer-related information or patient program assistance, please call 800-227-2345 any time day or night. Email Address (optional) Praise Dislike Suggestion What made your cancer.org website experience great?What made your cancer.org website experience challenging? 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Clothing during the early part of the 19 th century consisted of simple lines and bright, Oriental inspired colors. But, by mid century, widespread use of the sewing machine started a revolution in clothing akin to the industrial revolution that brought it to the forefront. The stronger stitches and faster methods presented the possibility for more intricate details and trim. The poorer class still sewed the clothing by hand. But, for those with the means, Victorian clothing began to take on the fussy characteristics that we commonly associate with the era. Womens Clothing For women, dressing was all about layers…and layer, and layers. It was typical to find, from the inside to the outside: Lace trimmed drawers made of cotton or linen A corset with boning to provide structure A camisole to cover the corset A hoop skirt Stockings attached to garters Petticoat(s) A very full skirt, some dresses for daytime even had a train A bodice, with additional boning, that fastened in the front Some kind of outer garment, such as a shawl Mitts or gloves Boots with button closures A hat or bonnet to cover the head Numerous accessories like handkerchiefs and fans All of the pieces would have been made from rich fabrics accented with elaborate twists, tucks, and trims. Women had special dresses for everything from mourning, to ball gowns, to outdoor recreation. The improved railway system made travel more efficient. It was fashionable to spend weekends “in the country” for recreation. The multiple activities meant that women spent much of their weekend changing their clothing. Mens Clothing Prosperity afforded more leisure time and men’s clothing began to reflect a more casual lifestyle. Drab knickers and fitted coat tails gave way to more colorful fabrics and flowing lines. Coats were longer and fuller and echoed the small waist silhouette of women’s clothing. As the era progressed, it became common to see men with colorful scarves or ascots. The Victorian fussiness was also apparent by the addition of scarf pins, cuff links, and heavy watch chains crossing the waist to a pocket. Men carried canes with intricate carvings and silver knobs. As the Victorian era neared its end, men were seen carrying accessories used for cigar smoking. And, in a trend that would last until the middle of the next century, men sported the single lens monocle associated with an English dude. Later Victorian Clothing It is no surprise that the approach of the 20th century found Victorians weary with all of the detail. Late Victorian clothing was becoming simpler with more muted colors. It was the beginning of a design movement that would, within a couple dozen years, progress to the streamlined deco style.

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MAVEN's top 10 discoveries at Mars MAVEN spacecraft and the limb of Mars. Credit: NASA's Goddard Space Flight Center On June 17, NASA's MAVEN (Mars Atmosphere and Volatile Evolution Mission) will celebrate 1,000 Earth days in orbit around the Red Planet. Since its launch in November 2013 and its orbit insertion in September 2014, MAVEN has been exploring the upper atmosphere of Mars. MAVEN is bringing insight to how the sun stripped Mars of most of its atmosphere, turning a planet once possibly habitable to microbial life into a barren desert world. "MAVEN has made tremendous discoveries about the Mars upper atmosphere and how it interacts with the sun and the solar wind," said Bruce Jakosky, MAVEN principal investigator from the University of Colorado, Boulder. "These are allowing us to understand not just the behavior of the atmosphere today, but how the atmosphere has changed through time." During its 1,000 days in orbit, MAVEN has made a multitude of exciting discoveries. Here is a countdown of the top 10 discoveries from the mission: 10. Imaging of the distribution of gaseous nitric oxide and ozone in the atmosphere shows complex behavior that was not expected, indicating that there are dynamical processes of exchange of gas between the lower and upper atmosphere that are not understood at present. 9. Some particles from the solar wind are able to penetrate unexpectedly deep into the upper atmosphere, rather than being diverted around the planet by the Martian ionosphere; this penetration is allowed by chemical reactions in the ionosphere that turn the charged particles of the solar wind into neutral atoms that are then able to penetrate deeply. 8. MAVEN made the first direct observations of a layer of metal ions in the Martian ionosphere, resulting from incoming interplanetary dust hitting the atmosphere. This layer is always present, but was enhanced dramatically by the close passage to Mars of Comet Siding Spring in October 2014. 7. MAVEN has identified two new types of aurora, termed "diffuse" and "proton" aurora; unlike how we think of most aurorae on Earth, these aurorae are unrelated to either a global or local magnetic field. 6. These aurorae are caused by an influx of particles from the sun ejected by different types of solar storms. When particles from these storms hit the Martian atmosphere, they also can increase the rate of loss of gas to space, by a factor of ten or more. 5. The interactions between the solar wind and the planet are unexpectedly complex. This results due to the lack of an intrinsic Martian magnetic field and the occurrence of small regions of magnetized crust that can affect the incoming solar wind on local and regional scales. The magnetosphere that results from the interactions varies on short timescales and is remarkably "lumpy" as a result. 4. MAVEN observed the full seasonal variation of hydrogen in the upper atmosphere, confirming that it varies by a factor of 10 throughout the year. The source of the hydrogen ultimately is water in the lower atmosphere, broken apart into hydrogen and oxygen by sunlight. This variation is unexpected and, as yet, not well understood. 3. MAVEN has used measurements of the isotopes in the upper atmosphere (atoms of the same composition but having different mass) to determine how much gas has been lost through time. These measurements suggest that 2/3 or more of the gas has been lost to space. 2. MAVEN has measured the rate at which the sun and the solar wind are stripping gas from the top of the atmosphere to space today, along with the details of the removal processes. Extrapolation of the loss rates into the ancient past—when the solar ultraviolet light and the solar wind were more intense—indicates that large amounts of gas have been lost to space through time. 1. The Mars atmosphere has been stripped away by the sun and the solar wind over time, changing the climate from a warmer and wetter environment early in history to the cold, dry climate that we see today. "We're excited that MAVEN is continuing its observations," said Gina DiBraccio, MAVEN project scientist from NASA's Goddard Space Flight Center in Greenbelt, Maryland. "It's now observing a second Martian year, and looking at the ways that the seasonal cycles and the solar cycle affect the system." MAVEN began its primary science mission on November 2014, and is the first spacecraft dedicated to understanding Mars' upper atmosphere. The goal of the mission is to determine the role that loss of atmospheric gas to space played in changing the Martian climate through time. MAVEN is studying the entire region from the top of the upper atmosphere all the way down to the lower atmosphere so that the connections between these regions can be understood.

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1. Introduction {#sec1} =============== The microbiomes, including bacteria, fungi, and viruses, live within and upon all organisms and have become a growing area of research. With the advances of new technologies it is now possible to entangle complex microbial communities found across animal kingdoms. Recent advances in molecular biology have provided new possibilities to investigate complex microbial communities and it has become clear that the vast majority of bacteria living in/on other animals cannot be cultured. It is now commonly accepted that at least 80% of the total bacterial species in the human gut cannot yet be cultured \[[@B1], [@B2]\]. High-throughput DNA sequencing approaches provide an attractive and cost-effective approach to investigate the composition and functions of the host microbiome. The culture-independent analysis of the host microbiome can be obtained by either metagenomic approaches or amplicon sequencing using specific marker genes. Amplicon sequencing provides a targeted version of metagenomics with a specific genetic region shared by the community members of interest. The amplified fragments derive from universal primers and are usually assumed to produce sequence read abundance that reflects the genetic diversity in the studied sample and hence sequence read abundance should reflect the genetic diversity in the studied sample. The amplified fragment typically contains phylogenetic or functional information, such as the 16S ribosomal RNA gene. 16S rRNA gene sequences are well studied and provide excellent tools for microbial community analysis \[[@B3]\], but other functional marker genes can also be used \[[@B4]\]. Subsequent taxonomy profiling of the entire microbial communities is conducted by comparisons to reference sequences or by*de novo*clustering of specific regions of sequences. Functional profiling of metagenomics is more challenging since major parts of the metagenomic data remain insufficiently characterized and frequently samples are contaminated by host DNA or traces from the diet. Compared to both culture-dependent and more traditional molecular approaches such as sequencing of clone libraries and DGGE, amplicon sequencing approaches allow a more in depth analysis of the complete microbiome and are less restricted to the number of samples to be investigated. For further technical details see, for example, Caporaso et al. \[[@B3]\]. 2. The Microbiome of Animals {#sec2} ============================ The Human Microbiome Project (HMP) \[[@B1]\] was initiated in 2007 and with this it has become clear that the human microbiome is highly diverse and complex. The number of microorganisms sharing the human body is thought to outnumber human cell numbers by a factor of ten and the combined microbiome usually contains 100x more genes than its host. The microbiome also plays a major role in human health \[[@B5]\] and both composition and alterations in the microbiome have been found associated with diabetes, inflammatory bowel disease, obesity, asthma, rheumatoid arthritis, and susceptibility to infections \[[@B10]--[@B11]\]. In recent years the microbiome of a number of vertebrate nonhuman species has been sequenced including livestock \[[@B12], [@B13]\] and wildlife species such as the Tasmanian devil \[[@B14]\], red panda \[[@B15]\], giant panda \[[@B16]\], black howler monkey \[[@B17]\], and koala \[[@B18]\]. Insects are the most diverse and abundant groups of animals on earth \[[@B19]\] and have colonized many different habitats. It is therefore not surprising that insect species are also inhabited by large and diverse microbial communities playing a pivotal role for insect biology. Many insect species are inhabited by a large and diverse assembly of microorganisms, where especially the microbial communities in the intestinal tract have received much attention \[[@B20]--[@B21]\]. Some insect species show a much more diverse microbiome compared to other insect species. For example, the microbiomes of some synanthropic flies, such as the green bottle fly, show high diversity compared to other species such as fruit flies or mosquitoes \[[@B25]--[@B23]\]. The high species richness could reflect the lifestyle of synanthropic flies, for example, breeding and living by animal manure, bedding, and/or decaying organic matter rich in microorganisms. The microbiome of other groups of invertebrates has also been established although for a limited number of species. Studies have compared the microbiome of different species of marine invertebrates with or without photosynthetic symbionts including five families of marine invertebrates \[[@B26]\]. Marine species of commercial interest such as oysters have also been addressed \[[@B27]\]. The microbes of soil invertebrates have received some attention. The gut microbes of soil animals play an indispensable role in the digestion of food and are of ecological importance in the global carbon cycle. Recently, research reported that like that of terrestrial insects some soil invertebrates such as collembolans, earthworms, and nematodes contain a rich microbiome and putative symbionts \[[@B29]--[@B30]\]. Further, results have shown how differences in diet among earthworm ecological groups lead to the establishment of different bacterial communities \[[@B29]\]. Moreover, perturbation of the soil ecosystem could impact earthworm gut wall-associated bacterial community composition and hence earthworm ecology and functioning. Even though the microbial community in invertebrates like that of collembolans and earthworms is not fully addressed, there is convincing evidence that intestinal communities can contribute to the degradation of recalcitrant biological materials such as chitin and lignocellulose \[[@B29], [@B28], [@B31]\]. 3. Factors Affecting the Animal Microbiome and the Biological Significance {#sec3} ========================================================================== To begin with all microorganisms were seen as pathogens causing infectious diseases to the host. The host immune system of eukaryotes was built to eliminate these intruders, but at the same time tolerating its own molecules. However, we now know that the association between eukaryotic hosts and the microorganisms is far more complex. With the advances in molecular biology, such as next generation sequencing, it is now possible more specifically to address the association between a host and its microbiome. In animals the association between the host and its microbiome can take many forms and includes symbiotic and pathogenic associations \[[@B20]\]. Symbiotic microbiomes can be beneficial to the hosts in many ways, including dietary supplementation, host immune system, and social interactions \[[@B22], [@B32]\]. In many insects, the gut symbionts are essential for survival and development and suggest the presence of a core microbiome \[[@B33]\]. The symbionts need not to be completely dependent on the host and animal-microbial interactions can be flexible and facultative and the host can carry different symbionts at different times \[[@B20]\]. The association between the host and the microbiome is also affected by a large number of abiotic and biotic factors and can involve the immune system, nutrition, reproduction, communication, and many other systems of the host \[[@B2], [@B34]--[@B36]\]. The number of studies addressing the role of the microbiome on animal health is limited and almost entirely restricted to human studies. However, a large number of studies have addressed the role of single bacterial symbionts on animal fitness, where especially insect species have received much attention \[[@B39]--[@B38]\]. There is now a growing interest in understanding what factors can affect the microbiome of animals in order to understand how fitness is affected and to explain differences between ecosystems, species, and/or populations. The composition of the bacterial communities of animals including invertebrates and vertebrates seems to be shaped by multiple factors, such as the host genotype \[[@B21], [@B25], [@B40], [@B41]\], diet \[[@B17], [@B34], [@B39], [@B42]\], life stage \[[@B43]\], laboratory rearing \[[@B34], [@B43], [@B44]\], and the ecological and physiological conditions of, for example, the gut of the insect \[[@B21]\]. Further, recent studies have proposed that the microbiome impacts the nutritional supplementation, tolerance to environmental perturbations, and maintenance and/or development of the immune system \[[@B20]\]. Some invertebrates lack the complexity and diversity of associations with microorganisms. Such insect model systems allow investigations that aim to understand the contribution of specific bacteria and the entire microbiome towards host physiological processes. For example,*Drosophila melanogaster* provide a promising model system to address some of these issues and for this species it is possible to rear axenic flies. Next generation sequencing approaches can provide an in-depth analysis of the functional roles of specific groups of bacteria and the entire microbiome on the fitness of the host. Results on*D. melanogaster* have shown how the microbiota affects developmental rate and changes metabolic rates and carbohydrate allocation under laboratory conditions \[[@B32]\]. Similarly functional analysis of the microbiome of ants also suggests large capacity to degrade cellulose \[[@B45]\] and that metabolic functions of microbes in herbivorous species play a role in fixing, recycling, or upgrading nitrogen \[[@B46]\]. Hypothesis has also been proposed to describe that gut microbiomes might facilitate insect herbivory and that variation in the ability to consume chemically defended plants can be partly explained by variation in the gut microbiome \[[@B47]\]. Recent studies have highlighted the importance of the microbiome not only in shaping the immune system but also in the context of host pathogen transmission processes (for reviews see \[[@B20], [@B48]\]). An example hereof is that the success of malaria infections is not only influenced by the mosquito innate immune responses and genetics but also affected by the composition of the gut microbiota and is in fact one of the major components affecting the outcome of mosquito infections \[[@B24]\]. Studies have also suggested that abiotic factors can affect the microbiome of disease vectors and thus vector competence of the host \[[@B23], [@B35]\]. Similarly the epidemics of human pathogens transmitted by insect vectors correlate with environmental factors \[[@B49], [@B50]\] suggesting that the vector competence of insect vectors is affected both indirectly and directly by environmental factors \[[@B35], [@B51], [@B52]\]. The recent interest in the importance of the microbiome on tolerance to environmental perturbations \[[@B37], [@B38]\] has revealed the presence of single bacterial species and mainly endosymbionts with large impact on, for example, temperature tolerance (for review see \[[@B38]\]). Temperature can affect the host directly or indirectly through either abundance of the symbiont or efficiency of transmission to the offspring \[[@B53]--[@B55]\]. At present it is unclear to what degree single strains of bacteria play a dominant role in tolerance to environmental factors or if interactions between bacteria of the microbiome are dominant. The recent advances in molecular biology and implementation of statistical analysis allow more specific hypothesis to be tested on effects of the microbiome on tolerance to, for example, environmental stress. 4. Conservation and Implications for Conservation {#sec4} ================================================= Changes in the microbial community have been shown to affect fitness of humans and other species as described above. However, the implications of changes in the microbiome for animal conservation have only been addressed in a limited number of studies even though the implications are many. Several studies using next generation sequencing approaches have addressed the comparison of the microbiome of laboratory populations or individuals kept in captivity with that of wild animals \[[@B14], [@B15], [@B18], [@B34], [@B44]\] or of single species in habitats influenced by different degrees of human behavior \[[@B17]\]. Results show that species across taxa living under laboratory conditions or affected by habitat fragmentation show less diverse microbiomes compared to wild species. Thus species are jeopardized not only directly by degraded habitats with reduced resource availability but also indirectly through diminished microbiomes. It is thus essential that future studies address the microbiome and how habitat fragmentation impacts the microbiome in different species and how species with less diverse microbiomes perform under these conditions. It is essential that we address the importance of the microbiome of other species rather than humans and the impact it has on their health status. For larger species such as primates this can be difficult and often only correlative evidence exists or can be achieved through a functional annotation of the microbiome \[[@B14], [@B17]\]. For example, in a study by Amato and coworkers \[[@B17]\] it was shown that beneficial fermenters, acetogens, and methanogen bacteria were more abundant in black howler monkeys inhabiting evergreen rainforest compared to individuals from fragmented habitats. The latter group also contained higher numbers of sulfate-reducing bacteria producing undesirable end products such as H~2~S. This strongly suggests that habitat fragmentation will affect not only the microbiome of the host but also host fitness. Similarly, keeping animals under captivity and maintaining breeding populations are likely to affect animal microbiomes. This is often undertaken in order to protect or increase abundance of rare species aiming at releasing species into the wild again. However, if the microbiomes of the individuals being released are affected, this is likely also to affect fitness compared to that of wild individuals and will subsequently reduce the probability of successful reintroduction into the wild. This is supported by studies on humans and mice where results have shown that obesity causes shifts in gut microbiome composition \[[@B10], [@B56]\]. Similar nutritional conditions could be expected for individuals kept in captivity. Molecular approaches allow researchers to establish entire microbiomes of animals and thus also test if, for example, it is possible to acclimate animals before being released into the wild. Optimizing environmental conditions of species in captivity could potentially ensure successful management and reintroduction. It has been suggested that engineering microbiomes can be used to improve plant and animal health \[[@B57]\]. How this can be incorporated into conservation is unclear. It is standard to employ basic principles of genetics into breeding strategies for endangered species in zoos or captivity, but the microbiomes evolutionary potential has been ignored also in conservation biology. Inbreeding has been suggested to affect the demography and persistence of natural populations and play an important role in conservation biology \[[@B58]\]. Recent work shows that inbreeding depression in bird and mammal populations significantly affects birth weight, survival, reproduction, and resistance to disease, predation, and environmental stress \[[@B59]\]. Inbreeding depression is expected to change the proportions of homozygotes and thus also heterozygotes. Consequently recessive deleterious mutations are likely to be expressed. As fitness of animal populations is expected to be affected by genotype of the host and the microbiome and interaction between the two it is also likely that the microbiome will be affected by inbreeding depression either directly or through interaction with the genotype of the host, not only because the genepool is diminished but also because of a compromised immune system. Microbiome analysis of wild populations has shown that the microbiome is dependent on the surrounding habitats as discussed above. This information might be used as a sensitive screening tool to establish populations affected by habitat fragmentation \[[@B17]\] and possibly also the effect of inbreeding. The strong signal from the diet \[[@B17], [@B34], [@B39], [@B42]\] suggests that the microbiome can also be used as a screening tool of diet preferences and to protect critical food resources or habitats for endangered species. However, it is essential that we fully understand the temporal and spatial changes in the microbiome if we are to use it as a screening tool. The microbiome can provide protection of the host from pathogens either through stimulation of the immune system or through competitive exclusion. However, when animals are compromised or exposed to unfavorable environmental conditions the symbionts themselves can act as opportunistic pathogens \[[@B2], [@B27]\] or not provide the same degree of protection. There are examples of how environmental conditions can affect the microbiome of invertebrates. For example, studies have shown how changes in temperature have caused shifts from mutualistic to pathogen dominated communities in corals \[[@B60]\]. In oysters temperatures over 20°C can cause summer mortalities, but temperatures as low as 14°C will promote development of brown ring disease in clams \[[@B61], [@B62]\]. This is important in conservation biology given the fact that species and populations are or will be exposed to changes in climate under the future climate scenarios. Host species will thus be exposed to not only the direct effects of changes in, for example, temperature but also indirect effects due to change in abundance or species composition of the microbiome. These changes can again lead to direct fitness effects on the host or indirect effects through changes or modification of the immune response. The microbiome could potentially also allow organisms to respond on a short timescale and cope with, for example, changes in climate. In particular, for species with a long generation time populations might not be able to adapt to fast changes in climate. However, bacteria with a short generation time can adapt on a shorter timescale compared to the host and may provide fitness advantages that allow the host to cope with changes in climate. Future studies should more specifically test if and how the microbiome affects animals ability to respond to a changing environment. Such plastic responses can have important implications for persistence of species or populations at risk in a fluctuating environment. Differences in microbiomes may affect invasions. For example, the interactions between native and nonnative of closely related species may be affected by the transmission of bacteria. This also appears to be associated with another emerging type of invasion, the transmission of infectious diseases of wild animals to humans \[[@B63]\]. Such transmission may be associated with factors including changes in human and nonhuman microbiomes. These interactions also have important implications for the conservation and management of different species within the environment. Some studies have addressed the microbiome of invasive species and also compared populations originating from the species native region with that of invasive regions \[[@B64], [@B65]\]. For the invasive snail,*Achatina fulica*results showed a highly diverse microbiome and functional analysis revealed a variety of microbial genes encoding enzymes, which is in agreement with the wide-ranging diet of this species \[[@B65]\]. Interestingly in another study comparing the microbiome of the soybean aphid,*Aphis glycines* from populations of native and invasive regions showed no differences \[[@B64]\]. Future studies should address the importance of the microbiome of invasive species to investigate if single strains of bacteria, the entire microbiome, or their interactions are major determinants for a species ability to establish in a new environment and if invasive microorganisms carried by introduced species affect native species \[[@B66]\]. 5. Conclusions {#sec5} ============== Recent advances in molecular biology have given new possibilities to establish complex microbial communities and it has become clear that the vast majority of bacteria living in/on other animals cannot be cultured. One of the most common methods to describe complex microbiomes is the sequencing of the bacterial marker 16S ribosomal RNA (16S rRNA) genes through amplicon sequencing. Studies have shown that the microbiome plays a major role in human health, and in recent years the microbiomes of an increasing number of nonhuman species have been investigated. However, the number of studies addressing the role of the microbiome on animal health still remains limited. Some studies have discussed the role of the microbiome on nutritional supplementation, tolerance to environmental perturbations, and maintenance and development of the immune system. Thus the implications of changes in the microbiome for animal conservation are many although a limited number of studies have addressed this. We suggest that a number of factors relevant in conservation biology could affect the microbiome of animals including inbreeding, habitat fragmentation, change in climate, and effect of keeping animals in captivity. Changes in these factors are thus also likely to affect the fitness of the host both directly and indirectly. With the development of next generation sequencing and functional analysis of microbiomes it has become possible more specifically to test direct hypothesis on the importance of the microbiome in conservation biology. This work was supported by the Danish Council for Independent Research (Grant no. 11-116256) (Simon Bahrndorff) and the Aalborg Zoo Conservation Foundation (AZCF). Competing Interests =================== The authors declare that there is no conflict of interests regarding the publication of this paper. [^1]: Academic Editor: Philippine Vergeer

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Coup de la Glotte Intending to encapsulate and codify the technique and style of the singers of the first forty years of the nineteenth century, Manuel Garcia based much of his ‘Treatise on the Art of Singing’ on the practice of his sister and his illustrious father. Within the previous decade both had died unexpectedly and early; his father, Manuel Vicente del Popolo Garcia, at 57 in 1832, and Maria Malibran, his sister, at the unbelievably early age of 28, in 1836. Garcia’s treatise rested on the teachings and method of his father, the teacher of both his son and daughter and whose youngest child, who was later to become Pauline Viardot-Garcia, had already started to play for his lessons by the age of eleven. From this small family came one of the most celebrated of all Rossini tenors – Manuel Garcia the elder; his son, the most influential teacher of all; and two of the century’s most illustrious singers – Malibran and Viardot-Garcia. Garcia senior had trained in Spain and later had studied with Giovanni Anzani, a famous bel canto tenor of the previous generation. So the precepts of the previous century, dominated by the castrati, flowed from his studio. All of the children were taught composition as well as singing, and both daughters followed their father in becoming composers themselves. Manuel Garcia, the younger, seems to have used his compositional talents to write vocal exercises and their accompaniments in his treatise. Part I describes the practice and techniques to become a good singer of the period and Part II, the style and use of the technique in performance. His work was based largely on his father’s and sister’s careers and that of their colleagues and contemporaries during the age of Rossini – the period which has become known as the Age of Bel Canto. Garcia’s attention to detail included not only breathing and other technical essentials, but also a description of the absolute beginning of the sound, known in Italian as attacco and in German as Ansatz. As he wrote in French, the initiation of the sound came out as the coup de la glotte – ‘shock of the glottis’. Poor Garcia! He can never have imagined the trouble and confusion this innocent phrase was to cause him for the rest of his days. During the last two decades of his long life, the vogue among voice teachers turned away from the bel canto precepts on which he had been brought up, and veered towards the new, but mistaken, concept of breath pressure theory. This determined that the vocal cords were activated only by a direct air blast from the lungs. In contrast, the ‘bel cantoists’ held that the tone was started by breath already controlled by the so-called ‘vocal struggle’ – la lotta vocale: the expiratory muscles being opposed by the inspiratory, thus allowing the breath flow at the chords to be controlled from the softest and most gentle tone to the strongest and loudest. Thus, the vocal cords never had to withstand forced air from below and therefore were always capable of vibrating freely and without strain. Because of the breath pressure theories – which continue up to the present day, alas – means were sought to take the strain away from the cords which such a strong air blast placed on them. So the tone was aimed as far away from them as possible: ‘in the ‘masque’; forward; behind the upper teeth; in the sinuses behind the nose; behind the eyes; on to the hard palate; anywhere, provided it was away from the larynx. The fact that vocal tone is generated entirely by the vibrating cords and the resultant sound resonating in the pharynx, was either ignored or disbelieved. The speed of sound (323 mps) was not taken into consideration at all, and the impossibility of aiming sound travelling at such a speed within an instrument only a few inches long was not contemplated. From this time, Garcia’s phrase, coup de la glotte, began to acquire sinister overtones which distorted and quickly anathematized the original meaning. A major element in this was a misunderstanding of the nuances of the French language, as Garcia’s treatise reached English speaking audiences. Coup literally means ‘shock’, ‘blow’, ‘knock’ in English, and is combined with genitive nouns for varied, specialised meanings. For example: coup de bec – peck; coup de tête – head butt; coup de poing – punch; coup de pied – kick; coup de coude – blow with the elbow or nudge; coup d’épée’ – sword thrust; and also more figurative meanings such as: coup de sifflet – whistle blast; coup de téléphone – telephone call; and coup de foudre – thunderbolt. As is clear from these latter phrases, the underlying meaning of coup is ‘an instantaneous action’, not an act of force or violence. Looked at from this semantic point of view, therefore, the phrase coup de la glotte does not necessarily presuppose a forceful action, but rather a sudden, clean start at the glottis. Garcia, of course, raised and educated vocally as he was, could never have contemplated anything else. In the century and a half which separates us from Garcia’s treatise, there has been much confusion and muddle as various theories have flared up and vanished, but during much of this time one enduring warning light has shone out – that the coup de la glotte is dangerous. It has been equated with a violent, unprotected blast of air at the cords, commonly known as the hard attack. However, logic would imply that if the breath is always controlled at the cords, then a hard unprotected attack is impossible. This is certainly what Garcia believed and a close reading of his section on the ‘Articulation of the Glottis’ shows this to be so. Without a clean start, either piano or forte, no word beginning with a vowel can commence. All vowels must have a precise start, he states. He is scathing on the practice of beginning vocal exercises with a consonant – la, ma, na, pa, etc. and explains that such practices disguise faulty articulation of the glottis. He is equally painstaking and forthright on the physical separation of vowels and consonants in Italian – the one emanating from the throat and the other located wholly in the mouth. In retrospect, it is easy to see how Garcia’s phrase became misunderstood and misinterpreted as the world changed during his 101 years. A fatal mixture of new ideas and careless translation caused his phrase, straightforward to a Frenchman, to be disbelieved, rejected, and later in the twentieth century, even reviled. Many generations of singers have been taught to recoil from the infamous ‘hard attack’ in horror. Their teachers seem never to have gone to the source and checked on Garcia’s words and meaning; thus confusion on this subject has gone on for over a century. Teachers and singers in every generation have been aware of the eighteenth century concept of the clean attack of the sound as an essential element in good vocal technique; and yet most have accepted that the coup de la glotte is something to beware of. Few have gone to the trouble to find out that his use of the phrase was a genuine attempt to describe the result that everyone seeks: a precise and exact onset so that the voice speaks immediately, without tension, violence or fuss. The need for such a start is paramount. One should never forget Garcia’s other memorable phrase – ‘Once the vocal cords become vibratile, all control over them is lost’. If the start of the sound is wrong or unhealthy, so is everything that follows.

3

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Treaty of Zadar The Treaty of Zadar, also known as the Treaty of Zara, was a peace treaty signed in Zadar, Dalmatia on February 18, 1358 by which the Venetian Republic lost influence over its Dalmatian holdings. The Treaty of Zadar ended hostilities between Louis I of Hungary/Croatia and the Republic of Venice, who were contesting control of a series of territories along the eastern Adriatic coastline in present-day Croatia. Background In 1301, the Árpád dynasty was dissolved and, following a brief interlude, was replaced by the Angevin dynasty as the rulers of Hungary and Croatia. The first Angevin king was Charles Robert, who ruled from 1312 to 1342. He was supported by the most powerful Croatian nobleman Pavao Šubić, Prince of Bribir and Ban (viceroy) of Croatia, ruler of the coastal cities of Split, Trogir, and Šibenik. Pavao became the Ban of Croatia, conferring on him many of the powers of a monarch including minting coinage, conferring charters on cities and levying annual taxes on them. Pavao's actions led to a revolt among the Croatian nobility, who successfully reached out to King Charles to help them remove Pavao. In exchange for his aide, however, the Croatian nobility was forced to declare their direct allegiance to the Hungarian monarchy, setting the stage for Hungarian attempts to expel the Venetian Republic from the Croatian coastline. While the other cities in the Dalmatian region were suffering from tug of war between the Venetians and the Hungarians and Croatians, Dubrovnik, which was held by Venice, was growing into an economic power house by exploiting its position between the west and the mineral-rich kingdoms of Serbia and Bosnia, as well as Dubrovnik's broader location between Europe and the Levant. In the 1350s King Louis I was able to assemble a force of 50,000 men by joining his forces with reinforcements sent by the Duke of Austria, the Counts of Gorizia, the Lord of Padua, Francesco I da Carrara, and the Patriarchate of Aquileia, a state within the Holy Roman Empire. In 1356, the coalition besieged the Venetians at Asolo, Conegliano, Ceneda and the stronghold of Treviso. At the same time, along the Dalmatian coast, the army had attacked the Croatian cities of Zadar, Trogir, Split and Dubrovnik, as well as other smaller towns that surrendered fairly quickly. Broken by a series of military reversals suffered in the territory under their control, the Venetians resigned themselves to the unfavorable conditions stipulated in the Treaty of Zadar, which was signed in the eponymous city on February 18, 1358. Consequences The treaty was signed in the Closter of Monastery of St. Francis and based on the terms of the agreement, the Dubrovnik region and Zadar came under the rule of the King of Hungary and Croatia. It marked the rise of the Republic of Ragusa as an independent and successful state. The same cannot be said for Zadar since it was later sold back to Venice by Ladislaus of Naples. As a result of the peace treaty, Venice had to give all its possessions in Dalmatia to the King, from the Kvarner to the Bay of Kotor, but could keep the Istrian coast and the Treviso region. It was also forced to cancel, in the title of its doge, any reference to Dalmatia. However, the treaty preserved Venice's naval predominance in the Adriatic Sea as the King Louis accepted not to build a fleet of his own. Louis and his army triumphantly entered Zadar in 1358 by granting extensive privileges to the nobility of Zadar and erecting the city capital of Dalmatia. See also List of treaties References External links Zadarski list Kako je i zašto Ladislav prodao Dalmaciju, June 7, 2008 Zadar Category:14th century in Croatia Category:Wars involving medieval Croatia Category:History of Zadar Zadar Category:Treaties of the Republic of Venice Zadar Category:Treaties of the Kingdom of Hungary (1000–1918) Category:History of Dalmatia Category:1358 in Europe Category:14th century in the Republic of Venice Category:14th-century military history of Croatia

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Kappa is a water demon whose mentions are found in ancient folklores of Japan. While some refute its existence by calling it a creature of imagination originating out of sightings of giant salamanders of Japan, others still hold the believe that Kappa is not confined to myths. In fact, some people actually consider that Kappa is very much real. Those who consider it to be real now have a support in their favor. Scientists have obtained very unusual mummified remains of a creature that are very much aligned with the characteristic features of the mythical demon. As a matter of fact, the discovered remains went for display in Kyuushuu island of Japan. How does a Kappa look like? The word Kappa literally translates into ‘river child’. The creature has been described to have a spiky and scaly body of a tortoise with a reptile-like blue or green skin. The limbs of the creature are described to be webbed and it is said to have a beak. If that isn’t just enough, what’s really unique to the creature is a hollow structure on top of its head. While the folklores say that Kappa is primarily a water creature, it also occasionally roams around on land. The hollow on its head is meant for holding water to keep it wet enough so that it does not loses its powers on land. What makes Kappa a demon? This lakes, rivers and ponds dwelling creature is said to be a demon. According to legends, the creature captures and devours children who are disobedient. What’s really interesting about this description is that Kappa turns out to be a selective demon. Kappas are often also depicted as mischief creators often attacking women and drowning animals and people. They are also said to make rude sounds as part of their mischievous behavior. About the mummified remains Scientists have gotten their hands on unusual mummified remains of a creature. The remains include an arm with attached hand and a foot. It is said that the remains were given to Miyakonijo Shimazu family in 1818 after one of the legendary creatures was shot dead. No other details are available. For instance, no one knows who shot the creature or why the rest of the body is not available. The remains went for display in Miyazaki prefecture at Miyakonijo Shimazu Residence. Scientific literature on Kappa During Japan’s Edo period, much of scientific work was devoted towards Kappa study. One such collection of Kappa information is Suikokouryaku of 1820. The information found in this compendium has information sourced from various Chinese and Japanese sources. Suikokouryaku contains several interesting drawings of Kappa. Killing a Kappa is not that difficult As per legends and folklore, Kappas are very much obsessed with manners. On land when someone bows, the Kappa will return the gesture by bowing. So in order to kill a Kappa, one should deep bow and as Kappa returns the gesture with a deep bow, the water in the hollow on its head falls off, rendering the Kappa powerless. It is then that a Kappa can be killed easily. Other mummies of Kappa Apart from the scattered remains obtained from the Miyakonijo Shimazu family, there are a number of other mummies on display which are claimed to be Kappa mummies. Some of these mummies are pictured above. Arguments by skeptics Skeptics say that all the mummies that are on display and are claimed to be Kappa mummies are not real. They say that these mummies are works of artists from Edo period that lasted from 1603 to 1867 and that they were created using different animal parts like monkeys, stingrays and owls. So, what do you think? Are Kappas real? Drop your comments below and let us know. 1 comment Theo Davis MannMarch 18, 2017 - 12:48 am I believe that the current American “fake news” fad/controversy is not NEARLY as interesting as this! At least here, you have some substance, quite literally, that can be objectively analyzed by science (although it doesn’t seem to be happening…where’s the DNA testing)- vs contentious 2-party politics that are just…… so pathetic and nonsensical.

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MyAccess Sign In About MyAccess If your institution subscribes to this resource, and you don't have a MyAccess Profile, please contact your library's reference desk for information on how to gain access to this resource from off-campus. Introduction The knee, which is a gliding hinge joint, is the largest synovial joint in the body. Its small area of contact of the bone ends at any one time makes it dependent on ligaments for its stability. Although this allows a much increased range of movement it does increase the susceptibility to injury, particularly from sporting activities. Finding the cause of a knee problem is one of the really difficult and challenging features of practice. It is useful to remember that peripheral pain receptors respond to a variety of stimuli. These include inflammation due either to inflammatory disorders or chemical irritation such as crystal synovitis, traction pain (e.g. trapped meniscus stretching the capsule), tension on the synovium capsule (e.g. effusion or haemarthrosis), and impact loading of the subchondral bone. Disorders of the knee account for about one presentation per 50 patients per year.1 The commoner presenting symptoms in order of frequency are pain, stiffness, swelling, clicking and locking.1 The age of presentation of a painful knee has varied significance as many conditions are age-related. Excessive strains across the knee, such as a valgus-producing force, are more likely to cause ligament injuries, while twisting injuries tend to cause meniscal tears. A ruptured anterior cruciate ligament (ACL) is a commonly missed injury of the knee.2 It should be suspected with a history of either a valgus strain or a sudden pivoting of the knee, often associated with a cracking or popping sensation. It is often associated with the rapid onset of haemarthrosis or inability to walk or weight-bear. A rapid onset of painful knee swelling (minutes to 1–4 hours) after injury indicates blood in the joint—haemarthrosis. Swelling over 1–2 days after injury indicates synovial fluid—traumatic synovitis. Any collateral ligament repair should be undertaken early but, if associated with ACL injuries, early surgery may result in knee stiffness. Thus, surgery is often delayed. With isolated ACL ruptures, early reconstruction is appropriate in the high-performance athlete; otherwise, delayed reconstruction is appropriate if there is clinical instability.3 Acute spontaneous inflammation of the knee may be part of a systemic condition such as rheumatoid arthritis, rheumatic fever, gout, pseudogout (chondrocalcinosis), a spondyloarthropathy (psoriasis, ankylosing spondylitis, reactive arthritis, bowel inflammation), Lyme disease and sarcoidosis.

3.0625

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X-rays and visible light from the radio galaxy 3C31, located 240 million light-years from Earth. Calculating how fast such galaxies spin doesn’t need to take dark matter into account, according to a new paper. X-ray: NASA / CXC / Univ. of Bristol / M. Hardcastle et al; Optical: NASA / STScI Some 80 years after dark matter was first theorised, we still have no idea what it is. Now, a new study casts doubt on its existence altogether. According to the standard model of cosmology, the immense gravity of dark matter is crucial for explaining why galaxies can spin so fast without tearing themselves apart. But in work just accepted by Physical Review Letters, a team of American astronomers found a striking correlation between the visible matter (the stars and dust in galaxies) and its rotation speed. That means they can predict the rotation of galaxies – without invoking the dark stuff at all. {%recommended 889%} “Nothing in the standard cosmological model predicts this and it is almost impossible to imagine how that model could be modified to explain it, without discarding the dark matter hypothesis completely,” said David Merritt, an astrophysicist at Rochester Institute of Technology in New York and who was not involved in the research. Gravity at the level of the solar system is a piece of cake. Simple laws, written by Johannes Kepler in the 1600s, tell us that a planet’s orbital speed depends precisely on its distance from the sun. So while Mercury whizzes around the sun at an average of 47 kilometres per second, Pluto shuffles along at just a 10th that speed. The weird thing is, galaxies don’t behave this way at all – stars don’t slow the further they are from the galactic centre. In some cases, they speed up. According to our current understanding of gravity, stars at the edges of galaxies, such as our sun, should be flung out into deep space. In the 1970s the American astronomer Vera Rubin, picking up an idea pitched by Swiss astronomer Franz Zwicky a few decades before, suggested an answer: there must be extra matter in and around the galaxies – perhaps 10 times more than what we can see – holding everything together. But after 40 years of fruitless searching, some physicists think the hunt for dark matter has been a wild goose chase. {%recommended 1150%} In the new work, a team led by Stacy McGaugh at Case Western Reserve University in Ohio found a direct relationship between the distribution of regular matter in a galaxy and its speed of rotation. This distribution held, even for galaxies thought to be dominated by dark matter. McGaugh’s team pored over data from 153 galaxies collected by NASA’s Spitzer Space Telescope. Imaging in the infrared, Spitzer can see both the stars and the immense clouds of dust between them – and these components allowed McGaugh’s team to calculate the mass of the visible matter in each galaxy more accurately than ever before. Then they compared these masses against the actual rotation speeds of each galaxy, which were clocked by astronomers for decades. Surprisingly, for dark matter advocates at least, the measurements showed a tight correlation. This means the team could look at a galaxy’s visible matter and predict its rate of spin. The relationship is strong enough to be termed a new law of nature, “a sort of Kepler’s law for rotating galaxies,” the authors write. The result was consistent over 2,693 data points across 153 galaxies with a huge variation in body shape – from dwarfs to giants, from spiral-armed or irregular beasts, some with central bulges and others without – all without accounting for dark matter. {%recommended 1936%} The question is, why? Perhaps our understanding of gravity is fundamentally wrong. One theory waiting in the wings is modified Newtonian dynamics which says that gravity behaves differently at very large distances. It has been successfully applied to galaxy rotation too. But it is far too early to throw dark matter out. For starters, there is plenty of evidence beyond galactic rotation that tells us dark matter must be out there. While McGaugh admits the findings could stem from modified gravity, it could also be telling us something about the nature of dark matter itself. For instance, the spread of dark matter and regular matter could be more intimately linked than previously thought. Besides, the new work shows correlation, rather than causation, but one that, in the words of the author, “demands explanation”. “Most importantly, whatever theory you want to build has to reproduce this,” says McGaugh.

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A man's chances of survival depended on how quickly his wound was treated. Modern warfare was now producing vast numbers of casualties requiring immediate treatment at the same time. This necessitated an efficient system that could immediately address a patient’s critical injuries close to the Front and then evacuate him to a medical unit in a safer zone. This network is known as the Medical Chain of evacuation or evacuation chain. The secret of success in treating large numbers of casualties was rapid evacuation. “All through the chain of Medical Units from the Front to the Base the wounded man is kept the very minimum of time to attend to his wounds, and then he is moved on, and kept on moving, until he reaches either the Base or Home..... The reason for rapid evacuation is twofold. Firstly, it is very bad for morale if troops see wounded men lying about in large numbers; and, secondly, unless Medical Units are cleared they lose their mobility, and also cannot deal with a fresh influx of wounded that might come in quite unexpectedly - e.g. from a surprise counter-attack.” [Lt/Col T B Nicholls R.A.M.C. ‘Organization, Strategy and Tactics of The Army Medical Services in War’] The rapid and successful evacuation of any casualties, whether on a battlefield or in civilian life, depends on three interdependent factors - time, space and transport. Time involves how quickly wounds receive first aid so infection does not set into the wound, and/or the casualty does not bleed to death. It also involves how quickly the casualty can get to someone with specialized knowledge or with specialist equipment. Abdominal wounds, for example, need to be operated on within six hours in order for the patient to survive. Transport involves what type of equipment can be used and/or is readily available to transport the casualty away from danger and to an appropriate medical facility. This process could involve the soldier walking or being transported on stretchers, horses, cars, trains, barges or ships. Space involves what is happening in the immediate area such as: how close can emergency services get without becoming casualties themselves? What is topography and how does it help or hinder? Is there enough space to set up a large medical facility close by or is there only enough room for a small one? With the above in mind, other factors had to be considered: • Mobility: All medical field units needed to be able to move at a moments notice. This was essential to ensure the fighting units had medical support during an advance or retreat. The procedure for a significant advance was for each medical unit to move forward to one already up and running in front of them. Therefore, the Regimental Aid Post would move forward in line with the fighting soldiers. An Advanced Dressing Station would then move forward to a Regimental Aid Post. The Main Dressing Station would move forward to an Advanced Dressing Station. A Casualty Clearing Station would move forward to a Main Dressing Station, and a Stationary Hospital would move to fill the gap between the Casualty Clearing Stations and the General Hospitals near the ports. In a retreat the procedure would be same but in the opposite direction. This was achieved by a small ‘light section’ of each unit moving forward immediately. They would provide care for the serious cases still housed in the unit ahead who were unable to be moved. The rest of the unit would then evacuate less serious cases, then would close, pack up and move. • Distances between medical units: Sometimes the nature or physical features of the area (due to unsuitable topography for motor transport, bad weather, or deteriorated land due to heavy shelling) prevented medical units from getting optimally close. In these situations Relay and/or Collecting Posts were set up where patients could be collected and transported by horse drawn ambulances. (These will be explained further in the Field Ambulance and Casualty Clearing Station sections) • Overlapping areas: During a major offensive, the front Line might cover some 5 to 6 miles with many Corps/Brigades/Regiments involved, all of which would have had their own pre-allocated medical support. In situations where the areas of advance were narrow, it was inevitable that their medical support would overlap. In these cases medical units from different Divisions would either work together as one, or perhaps two or three different medical units would set up in one specific location. • Co-Operation: It was imperative that the medical evacuation chain did not hinder the fighting troops going into action or prevent them from getting to their ammunition, and vise-versa. Also the Medical Services was reliant on other branches of the army to supply materials to build Dressing Stations, construct roads, railway sidings, and/or provide telephonic communications. • Before the start of any major offensive the Directors and Assistant Directors of Medical Services (DMS and ADMS) who were appointed to oversee in the offensive held a conference to discuss all the above factors before setting up the evacuation chain for that sector. Collecting Zone: Regimental Aid Posts and Field Ambulances Regimental Aid Post. [RAP] and the role of the Regimental Medical Officer [RMO] “I should not advise anyone with any desire to practice their surgical or medical skill to take on the job of medical officer to a battalion, but from the point of view of seeing the war, understanding military methods and the spirit of the men it is the best post open to a medical man..... The only diseases the M.O. is called upon to treat are slight sprains, myalgia, and last, but not least, diarrhea.... Sanitation is, perhaps, the most important work that the M.O. is called upon to perform.” [Lt A Noel Garrod R.A.M.C. ‘Notes on the Existence of a Regimental M.O. - At the Front’] Duties of the RMO: During the war every fighting unit (infantry battalion, artillery brigade or cavalry regiment) had it’s own doctor [or RMO]. He was RAMC but came under the commanding officer of the fighting unit he was attached to. The doctor’s role was not only to attend to medical matters but also matters of hygiene, which meant water supply, the preparation of food, and the supervision of sanitary areas all came under his control. The doctor’s daily routine usually began with him doing an inspection of the sick. He then inspected the camp or billets, and the cook houses. The rest of the day would be taken up with the training and supervision of water cart orderlies and stretcher-bearers. To assist him in his duties he would have had an RAMC Sergeant or Corporal attached to him and perhaps 1 or 2 RAMC Privates. When away from the Front Line, the doctor’s post was known as the Camp Reception Station [CRS] or Medical Inspection Room [MI Room] and contained 2 - 6 beds for short term holding for those needing rest but was not sick enough to be evacuated back. “A good M.O. to a battalion was a privileged and important officer. He was usually on intimate terms with his colonel, a friend to all his brother officers, and friend and confidant as well as doctor to the rank and file. Often and often I noticed that a battalion with a first-class M.O. was always a first-class battalion, had the smallest sick parade, fewer men falling out on a long march and the lowest quota of casualties from trench foot.” [Capt Philip Gosse R.A.M.C. ‘Memoirs of a Camp-Follower’ Function of the RAP: When in the trenches the doctor’s post was the RAP. The objective of the exercise was to patch up the wounded and either return them to their duties in the line or pass them back to a Field Ambulance. The RMO had the same staff as mentioned above but this became augmented by a designated number of Stretcher-Bearers. These Regimental Stretcher Bearers came from the fighting unit the RMO was attached to, usually the regimental bandsmen. When under pressure, the RMO could be further assisted with bearer teams from a Field Ambulance. Every soldier had a special pocket in his uniform for his issued ‘First Field Dressing.’ It contained antiseptic pads and two bandages (one for entry wound, one for exit) in a waterproof cover. This dressing was applied by a regimental stretcher-bearer, a comrade, or by the wounded soldier himself, if he was able, in the firing line. If the wounded man was unable to walk, he was carried back via hand or wheeled stretcher to the RAP. The regiment stretcher-bearers had then fulfilled their duty, and it became the RMO’s responsibility for receiving the wounded man, and treating him by checking the dressing, overseeing the splinting of fractures, and ensure everything was being done to stop the patient going into shock. If morphine was given or a tourniquet applied, the soldier’s forehead was marked with a “M” or “T”. If required he would undertake an emergency amputation but large operative treatments were discouraged so close to the fighting and danger. The RMO also completed a Field Medical Card for each patient and fixed it firmly to the patient—generally attaching it to a button by its attached string. This card included the soldier’s name, rank, and unit, a diagnosis, and any special treatments (like operations) performed. As the patient moved down the evacuation chain, the Field Medical Card remained with him so that information could be added to it and his full treatment could be known. The patient was then taken to a designated collecting area to be picked up by stretcher-bearers of the Field Ambulance. Equipment: According to Dr John S G Blair “The basic MO’s drug box in 1914 included phenacetin for headaches, Adrenaline in injectable form, 0.0003gm, one dose to be used as a stimulant.... Dover’s powders for colds, Bismuth salicylate for the stomach, cough medicine, a light aperient calomel, and a strong one, unspecified; quinine sulphate, 2gr (60mg) as a tonic, lead and opium tablets to be made into a lotion as an application for sprains or as an anti-diarrhoeal and, for the doctor to hold safely, morphine sulphate gr 1/4 or grl 1/2 (15 or 30mg). Morphine was to be given “under the tongue or by injection.” There were also methylated spirits, iodine, boric lotion and carbolic acid 1 part in 60 as antiseptics for wounds, Lastly there was sal volatile, to be given for ‘fainting, a few drops in water’.” [Dr John S G Blair ‘Centenary History of The Royal Army Medical Corps]. Equipment at the RAP was supplied by the Field Ambulances and normally consisted of a primus stove and a beatrice stove, along with an acetylene lamp, anti-tetanus serum, assorted bandages, blankets, Boric ointment, cotton wool, first field dressings, plain gauze, shell dressings, Sulphur ointment and a vermoral sprayer. There was also reserve boxes of all of the above, and a hamper containing medical comforts such as brandy, cocoa, bovril, oxo, biscuits etc. Site (time and space): Location requirements: The site of the RAP came under the concern of the officer commanding the fighting unit. It was ideally situated a few metres behind the front line, but near the regiment’s headquarters so the RMO could be provided with early information about the tactical situation. It was also to be located central so it could be easily accessed from any part of the front line in which the regiment is engaged by the wounded. Also in a place that was sheltered to protect all from enemy fire, and easily accessible to the field ambulances who were next in the line of evacuation. Typical facility: RAP’s were usually situated in a dugout, in a communication trench, a ruined house, or a deep shell hole. In areas where constant fighting had occurred over a long period of time, such as Ypres, there was very little cover left so a RAP might have been set up behind a burnt out tank. RAP’s had no holding capacity for the wounded. If the engagement was successful then the RMO moved forward and searched out another area which would come into the above criteria. A yellow flag was put up so that the wounded could find it and runners might be expected to run back to advise the ADMS and the Field Ambulances of the new location. Transport: The RMO was equipped with a horse for his personal use, and a Maltese Cart (a two-wheeled cart suitable for conveying a lying patient) and driver. Alternatively these might have been a light motor van and a small motor-car or a motor-cycle combination. As noted above the RAP would have stretchers for hand carriage and/or wheeled stretchers. The Field Ambulance (of infantry divisions) General definition The Field Ambulance was a complete medical unit made up of previously separate and independent entities. These were The Bearer Division [previously working as Bearer Companies]; The Tent Division [previously working as Field Hospitals] and The Transport Division [Army Service Corps (to be explained further in the Transport of Sick and Wounded section)]. Personnel The Field Ambulance at full strength composed of 10 Officers and 224 men. The Bearer Division had 18 stretcher squads each of 6 men. The Tent Division was comprised of doctors: 9 medical officers and 1 dental officer, as well as 1 Quartermaster of stores, batmen, clerks, cooks, dispensers, nursing orderlies, and the Transport Division, which had 60 men attached from the Army Service Corps. All this made up medical support for one infantry brigade. [Three to every Division]. Each brigade was made up of three to four battalions, so in order to perform it’s duties satisfactorily, the field ambulance was divided into A, B and C Sections These three sections were all capable of carrying out independent action. The headquarters of the Field Ambulance always formed part of ‘A’ Section. The three sections were further sub-divided into three parts to incorporate the bearer division, the tent division and the transport division. Function of the Field Ambulance When away from the trenches a field ambulance’s role was to keep the fighting men fit and healthy. This was achieved by setting up Divisional Rest Stations [DRS] and baths (usually sited in a Brewery where up to 50 men could be bathed at a time in the large vats). They were also allocated special tasks such as providing treatment at scabies centers or other ailments. When in the trenches its role was similar to modern day emergency ambulance services: to collect and transport patients to someone with specialized knowledge or to specialist equipment, whilst monitoring them, and treating them if necessary to ensure their condition remains stable. The personnel serving in the field ambulance achieved this by setting up various designated posts and sections according to distance from the RAPs to the Casualty Clearing Stations. The Bearer Division were the stretcher-bearers responsible for collecting the wounded, whilst the Tent Division were the medical staff responsible for the treatment of their wounds. Before any major offensive, the three Field Ambulances of a Division joined together and acted as one to form and oversee the various posts and stations. One way of knowing how the field ambulances were arranged for any particular battle is to look at the war diary of the ADMS of that Division. The various designated posts and sections of a Field Ambulance: Advanced Dressing Stations [ADS]: Location and Construction: There were normally two ADSs to every Division. In areas where the Divisional line became narrow one ADS would be established for the sole use of that Division and one would be shared with the Division to their left or their right. ADSs were set up as far forward as military conditions would permit. Ideally, this was about 400 yards behind the RAPs. Preferable locations were large houses, schools or churches but tents were used where necessary. In all events they needed to provide living accommodation for the officers and men; shelter from the weather; be inconspicuous and provide protection from the enemy, and had to be easily accessible with an entrance and an exit. Personnel: The personnel of each ADS were 3 officers and 53 ordinary ranks. Of these 1 officer was the Officer Commanding. 36 Privates would be employed as stretcher-bearers, with 1 officer supervising them. The others would be employed as clerks, dressers and cooks. If the ADS became overwhelmed with casualties the above personnel could increase. Equipment: Typical equipment for the ADS included stretchers, notice boards and flags for marking routes, empty petrol tins for water and kettles, hot water bottles, acetylene lamps, blankets, ground sheets, pyjama suits, stomach warmers, anti-tetanus serum, chloroform and No 1 Field Pannier, which included: wool, gauze, plain lint, shell dressings, 3 and 6 inch and triangular bandages, a jaconet and a calico, towels, nail brushes, safety pins, plasters, towels, tourniquets, a tincture of iodine, rum jars filled with eusol, and splints for leg and back as well as the Thomas splint. Duties: The ADS was the first line of documentation for the RAMC, [i.e. Admission and Discharge books, war diaries etc]. Stretcher-bearers went forward and collected the sick and wounded from the RAP and carried them back to the ADS. A patient’s medical condition was then assessed to make sure bandages had not loosened or become too tight, and also that the patient was not haemorrhaging or going into shock. Special attention was given to those marked with a “M” or “T” (morphine or tourniquet) at the RAP, and careful examination was given to see if the tourniquet needed to remain or not. Surgery was not undertaken at an ADS unless absolutely necessary as it had no holding capacity. It was simply an intermediate stop to assess the patient. Those who were deemed to be urgent cases were transferred to the Main Dressing Station. Those who were not deemed as urgent cases were transferred straight to the Casualty Clearing Stations. “It was now eleven o’clock of a pitch black night with threatening rain... We were in for a busy night, for all the stretcher parties from the various ambulances were out in the field collecting the wounded, whose arrival was expected now at any moment. An operating tent had been pitched in the field near by, and was brilliantly lit up with a huge acetylene lamp. The operating table was fixed in the centre of the tent and along each side were the instruments, basins, and dressings lying on the lids of the panniers, which made excellent side-tables. Very soon the ambulances lumbered up with the men picked up from the fields close at hand. The stretchers, each holding a wounded man, were taken out of the waggons and laid on a heap of straw near the door of the operating tent. Sixteen men were taken out and laid side by side. New Stretchers were put in the waggons, which again set out to bring in more wounded. One surgeon stood on one side of the operating table, another stood opposite him, and a third surgeon was ready to assist or give an anaesthetic if necessary. Quietly and quickly one wounded man after another was lifted on to the table, his wounds were speedily dressed, and he was again carried out and laid on the straw with a blanket below and another above him. Those with painful wounds were given hypodermics of morphia. All who were fit to take nourishment had hot soup, tea, bread and jam. Stimulants were given freely to those requiring it. The wounds were mostly from shrapnel, and only one case required an anaesthetic. He had a bad compound fracture of the thigh and was in terrible pain. We made some good splints and fixed up the limb comfortably and in good position. One poor devil had a bad abdominal wound for which we could do nothing. He was given a good dose of morphia and slept quietly till five a.m., when he ceased to breathe. At one o’clock in the morning wounded were still coming in, and the surgeon on duty was relieved by myself. So with coat off, bare arms and covered with an operating apron, I did my spell of surgical duty during that night on the banks of the Marne. Our stretcher parties at last were finished, and had all come in with the report that all wounded had been brought in...... At six o’clock our large list of wounded were sent off the railhead at Coulommiers on returning-empty supply waggons and under the charge of a medical officer. The operating tent was struck and all the panniers and equipment were packed. The Field Ambulance had done its ‘job’.” [Lt Arthur Anderson Martin R.A.M.C. ‘A Surgeon in Khaki’] Main Dressing Stations [MDS]: Location and Construction: There was normally one MDS to every Division. They were formed by the Headquarters of the Field Ambulance [section A]. Ideally MDSs were sited roughly one-mile behind the ADSs. But in the Great War this was seldom the case, partly due to topography, but also because a MDS needed approximately 300 X 200 yards of space to provide sufficient room should it be taken over by a Casualty Clearing Station during an advance. The ideal location was a large building where water, light, heating and drainage were already supplied. If no buildings were available, then roughly 9 tents were used, with 1 reserved as an operating room. MDSs needed to be located between the ADS and the Casualty Clearing Stations, closer to the latter if possible. They did not need protection from shell fire, but cover from the splinters of bombs had to be taken into account. Structure: Every MDS was organised with six sections: 1) Receiving Section provided hot drinks, sandwiches, and cigarettes. 2) Recording Section where clerks took patient information and examined Field Medical cards 3) Resuscitation Section for warming and reviving those suffering from shock or the effects of haemorrhage. 4) Dressing Station where dressing were applied, and any urgent surgical treatment, administration of A.T.S. or morphia, if not carried out already. 5) Gas Section to keep gas victims away from other patients. 6) Evacuation Section where the patient’s treatment was classified with whatever they were suffering from and how they were treated, and they awaited evacuation. Other space was allocated for a mortuary, a cookhouse, stores, and living accommodation for officers and others ranks. Personnel: The personnel of each MDS included the Officer Commanding, 2 Medical Officers, a Dental Officer, a Quartermaster and 59 other RAMC ranks, along with 1 Royal Army Service Corps officer, and 44 other ranks ASC attached. Equipment: Typical equipment at the MDS was very much the same as the ADS, with additions of oxygen apparatus, operating lamps collapsible trestles and a field dental outfit. Duties: The MDS was further away from the firing line so was able to be better equipped to provide accommodation and treatment than an ADS. Urgent operations were more readily performed, and better arrangements could be provided for the resuscitation of those suffering from shock or haemorrhage, or both. Walking Wounded Collecting Posts [WWCP] During a major offensive the ADS quickly became congested. If it were pre-judged that this was likely to happen, then a WWCP was set up - one to every Division. It was generally believed that the walking wounded were able to walk slightly farther than the ADS, therefore a WWCP was often constructed at a location between the ADS and the MDS. Location: Ideally, a WWCP was sited with easy access from the front line and the ADS, and also close to a road leading to a Casualty Clearing Station so that transport could reach it. The route was set up close to the stretcher-bearers’ route in case the walking wounded man collapsed on his way to the WWCP. The route from the Front to the WWCP was clearly marked with notice boards or directing flags. The Post would have been sited behind the usual range of artillery fire but protection from splinters was accounted for it when a location was being formed - usually in a building or farm house but marquees were also used. Personnel & Equipment: The WWCP was staffed by personnel from a Field Ambulance section, but there were no specific arrangements, and there was no scale laid down for equipment. A suggested guide for equipment was 5 Thomas Splints, stretchers, blankets, waterproof sheets, soyer’s stoves, camp kettles, petrol tins for water, drinking mugs, and one medical companion and first medical panniers (pairs). Also dressings and light refreshments for approximately 300 cases. Structure: Similar to the MDS, the WWCP consisted of a Reception Section, a Recording Section, a Dressing Section, and an Evacuation Section. No operations or complicated dressing were done at the Posts. When leaving the Post, the wounded men were transferred to the MDS or the Casualty Clearing Station, whichever was deemed appropriate. Bearer Relay Posts [BRP] At times when it was impossible to get the ADSs optimally close to the fighting units due to unsuitable topography for motor transport, bad weather, or deteriorated land due to heavy shelling, the field ambulance set up relay posts. It was acknowledged at the time that bearers could not carry loaded stretchers more than half a mile over difficult ground, meaning that a relay post would be set up roughly every half a mile. There were no medical facilities set up at relay posts, they merely existed so that stretcher-bearers could pass their carry to the next set of stretcher-bearers and then return to the RAP to pick up new casualties needing to be carried. Collecting Posts [BCP, CCP or DCP] Collecting posts were set up where two or more evacuation routes met on the main route back from the Front lines. These could be Bearer Collecting Posts, where two or more relay posts merged, or could be set up further away from the front lines when evacuation routes from different Divisions or different Corps came together. Collecting Posts were mainly a holding area for wounded whilst they waited to be collected by either motor or horse transport. Although there were no medical facilities set up at these posts, they were often staffed by personnel from a Field Ambulance section to check dressings and supply a drink or something to eat. Transport Casualties were transport from the ADSs to the MDSs and Casualty Clearing Stations via horse wagons and motor ambulances. (to be explained further in the Transport of Sick and Wounded section) The Cavalry Field Ambulance (of cavalry divisions) General Definition: The definition and function of the Cavalry Field Ambulance was the same as the Infantry Field Ambulance. The difference is that is was smaller and because cavalry regiments were much more mobile than infantry regiments, their Field Ambulances had to be much more mobile. They would open, treat the wounded, then close and move much more frequently. “In view of the high degree of mobility requisite and the frequent moves that may be necessary, the personnel must be highly trained. Each man must know his job, and must be able to do it speedily. Loading, unloading, pitching and striking the shelter, together with arranging the equipment, must be practiced until this can be done in the minimum of time. An efficient team can establish the ADS in 10 mins” [Lt.Col E C Sandilands, RAMC ‘Journal of the RAMC, September 1935.] Personnel: Their personnel consisted of 6 Officers and 70 other ranks, RAMC. There were four Field Ambulances per Cavalry Division, each sub-divided into two sections; ‘A’ Section and ‘B’ Section. Procedure: “The usual procedure in action is that the ambulance is divided into tent and bearer sections, the former of which establish a temporary hospital of fifty beds some five miles behind the firing line. The bearer section goes forward and gets into touch with the regiment attached R.A.M.C. Officer at this regimental aid post when the cavalry are engaged in reconnaissance. From the aid post they will move cases in light wagons to the temporary hospital...... Professional work for officers consists of emergency operations and quick evacuation of wounded to the lines of communication. It does not burden itself with chronic cases, as it is a highly mobile force and must be ready to move forward at the shortest possible notice in conjunction with the cavalry brigade.” [Maj H Norman Barnett R.A.M.C. ‘The Work of a Cavalry Field Ambulance’] Evacuation Zone - Casualty Clearing Station. [CCS]. Main function: Casualty Clearing Stations were the pivot point in which the whole system of evacuation turned from collecting casualties to distributing them. When created in 1907, they were intended to act as sorting centres to facilitate the movement of casualties from the Field Ambulances onto the Base Hospitals. Their role was to act as a temporary reception area for the sick and wounded, and their prime duty was to arrange for and prepare patients for satisfactory evacuation rather than of active treatment. Their function, therefore, was similar to those of the Tent Division of a Field Ambulance but dealing with larger numbers of casualties and out of range of shell fire. As they evolved, however, their role became similar to modern day Accident and Emergency (A&E) Departments. Casualties were received, assessed, then divided into three categories (known today as triage). These categories were: Non-serious cases - to be returned to duty after recuperation and rest. Serious cases but still fit to travel - to be immediately evacuated back to the base hospitals. Serious cases in urgent need of immediate treatment. Casualties were provided with food and rest, and were prepared for their further journey, which could have been immediate or after recuperation. The main objective was to provide necessary treatment and move patients out as quickly as possible. However, as a result of their evolution and expansion, it became possible for recuperating patients to be retained for up to four weeks before being returned to their units or transferred to a General Hospital via Ambulance Trains or Inland Water Transport (barge). Evolution of their function: The discussion of CCSs is difficult to generalize because they were the one link in the evacuation chain that radically evolved over the course of the war. The CCS of 1914 was not the CCS of 1918. 1914 and 1915: CCSs mobilized in August 1914 under the title ‘Clearing Hospitals’. During the 1914 retreat, the equipment of most of the Clearing Hospitals was still in transit, consequently, they did not start to become fully effective units until early 1915. By this time it had become obvious to the medical services that there was public and professional confusion about the CCS’s role. Was it a sorting centre or a hospital as it’s title suggested? This resulted in their official title being changed to ‘Casualty Clearing Station’. In spite of the name change, very high volumes of urgent cases, (i.e, gas gangrene or abdominal injuries) arrived at the CCSs at an alarming rate. Unequipped to deal with this influx, in early 1915, the Director General of Medical Services (D.G.M.S.) approved the increase of surgical work and appropriated extra surgical equipment to be moved forward from the hospitals to the CCSs. By the middle of 1915 it became standard practice for head injuries, compound fractures, and penetrating wounds of the limb to be sent straight to CCSs. 1916: Despite surgery now taking place in CCSs, surgeons began arguing that facilities were required to enable surgery to take place even closer to the Front lines, to prevent a potentially fatal delay in the treatment of infected wounds. Post mortums of abdominal cases had revealed that most had died of hemorrhaging, which might have been avoided by earlier surgery. It was argued that Field Ambulances were not able to provide such facilities because of post-operative care - it was not advisable to move patients immediately after an operation and Field Ambulances were frequently on the move. Also, they were not in a position to provide patients with comfortable beds or nursing care, thus hindering a patients’ recuperation time, Arrangements for sterilizing instruments and gowns etc were also more difficult at Field Ambulances. All evidence indicated that the success rate for abdominal surgery was much higher when performed at CCSs rather than Field Ambulances, so all in all it was decided to bring CCSs in as close as 10,000 yards from the Front lines as opposed to roughly 20 kilometers away. This, however, resulted in them now coming under enemy attack, especially from aircraft bombing. Their positioning at railheads meant that CCSs were now becoming static and, despite the name change, were becoming more like hospitals. In some areas though, it was impossible to bring a CCS very close due to unfavourable topography. This resulted in the formation of Advanced Operating Centres and Abdominal Hospitals. (see ‘Formation’ section) 1917: By 1917, more operations were performed at CCSs than base hospitals. From 24th July 1917, the distribution of sick and wounded to CCSs was regulated in accordance of the D.M.S. of the Fifth Army to treat certain types of wounds. The Field Ambulances became the sorting centres, separating, for example head wounds from stomach wounds at the ADSs, and transporting them to the relevant CCS. Specific CCSs were also allocated to treat self-inflicted wounds, as well as infectious cases, and those who were gassed. Other measures established at CCSs in 1917 were surgical cleaning of wounds before evacuation to the base, the principle of retaining so-called shell shock cases, and measures to deal with mustard gas, which was used by the enemy for the time in 1917. Also by 1917 nursing sisters were successfully trained in the administration of anaesthetics, which was successful and freed up more than a hundred medical officers for other duties. 1918: The spring 1918 German offensive placed the CCSs in danger of becoming part of front line action, which caused them to become mobile again and retreat. By June 1918 they had reduced in size, and many had lost their equipment to the enemy - some sent by transport to a different location, and some taken by the enemy. They were no longer situated on railheads or in other areas designed to promote easy evacuation of the wounded because they had been on the move. By the time of the Allied Counter-Offensive in August, they had recovered their losses, but it was agreed, that although they would be placed as far forward as possible, they must remain sufficiently mobile to keep up pace with any advance or retreat. Personnel: In normal circumstances CCS personnel would included 8 Medical Officers (The C/O, 6 doctors, and 1 surgical specialist), 1 Quartermaster, 7 QAIMNS, and 77 other ranks (working as clerks, cooks, nursing orderlies, theatre orderlies, stretcher-bearers etc.) Often a dentist and a pathologist were attached. Non-medical personnel attached would include 3 chaplains, 4 lorry drivers, 2 Royal Engineers personnel - an electrician and engine hand, and men from the Army Service Corps, employed as ambulance drivers. This small staff was sufficient in quiet times but totally inadequate during battle. In times of heavy fighting, the number of personnel could be increased and specialized by bringing ‘Surgical Teams’ forward. A surgical team was made up of a surgeon, an anaesthetist, a theatre sister, 2 theatre orderlies, 4 stretcher bearers, and a batman. The extra personnel were brought in from hospitals at the base, or from CCSs and/or Field Ambulances which were not engaged in active operations. Additional nursing sisters were also attached in proportion from 7 to 24 or more. The organization for reinforcements during a major battle gave no provision for additional rank and file, (i.e. men to assist with the unloading of motor ambulance cars as they came in, and loading patients onto ambulance trains.) To meet this demand, detachments of 50 or more low category men, or men from labour companies or other sources, or even convalescent patients were attached to CCSs. Formation/Location: As a general rule there was one CCS per Division. It was found, though, that 10 CCSs were sufficient to treat the wounded in most major offensives. This allowed surplus CCSs to be employed for the reception of sick, infectious diseases, or special cases, such as head wounds, abdominal wounds, etc. In September 1916, every CCS was divided into a heavy and a light section. The light section was designed to be able to move forward or retire in line with the troops at a moment’s notice. A light section was also used to set up Advanced Operating Centres or Abdominal Hospitals. CCSs usually worked in groups of twos or threes, and in relay. This meant one would be closed and treating casualties for evacuation by train or ambulance to the Base Area, whilst the other would be empty and readying itself to receive new casualties. When the second one became full it would close, but the first would by now be empty and ready to receive new casualties again. A third would only be treating the sick, but would evacuate to receive battle casualties in an emergency. Each CCS took around 150 to 200 wounded before they closed and new patients arriving were redirected to another CCS. Early CCSs were established in buildings, but with the need for expansion, they began setting up on open ground, using tents and hospital Nissen huts. When on open ground they were situated near a railway siding for their own use, with a good road and communication towards the Front. The tents and huts provided accommodation for staff, and wounded, as well as operating theatres, medical and surgical stores, kitchens, sanitation, incineration plant, ablutions, and a mortuary. Portable generators were supplied to provide lighting. The conditions which determined the selection of sites for CCSs were: proximity to railways, good road approaches, reasonable security from hostile artillery fire, and adequate water supply. Capacity: Early CCSs were set up to provide accommodation for 200 patients, however the number of surgical operations being performed by 1917 meant they had expanded greatly, and were able to receive between 800 - 1,200 sick and wounded. Procedure: The standard system of receiving and treating casualties arriving at a CCS meant patients would go through: The stretcher exchange dump - where the drivers of motor ambulances delivered casualties and exchanged the equivalent of equipment handed in. A general admission tent or hut, or a receiving section - where a patient’s particulars were recorded in an Admission and Discharge (A & D) book, and his medical condition was classified by a medical officer. Refreshments such as tea, coffee, hot soup, sandwiches, and cigarettes were supplied here for waiting patients. A patient might then go to: A section for the dressing of walking patients: Here a patient might sit on benches, where he was attended to by a sister and/or orderlies working under a medical officer. A section for the dressing of lying down patients: Stretcher cases were carried here. If the patient’s wound was slight, it would be dressed, and the patient was then taken to the evacuation ward. If his wounds were more serious he was passed on to the pre-operation ward. A pre-operation section: Here the patient’s clothes were cut away, and he was cleansed, warmed and fed. A resuscitation ward: If on arrival the patient’s condition was too unstable for surgery, he was taken to the resuscitation ward, where a medical officer, a sister, and orderlies attended to his revivification. He was rested, warmed, infused or transfused - whichever might have been necessary. X-ray department: There were six mobile X-Ray units serving in the British Expeditionary Force during the Great War and these were sent to assist the CCS's during the great battles. Operating theatre: After 1916 there could be one or two theatres accommodating up to 12 tables arranged in pairs, each pair being divided from the other to provide privacy. Two tables were often provided for each team in order to save time. Surgical teams often worked in groups of 3 for 8 hours shifts with 4 hours off to sleep. This pattern could enable two operating tables to run continuously for a week. In reality, different CCSs worked in different ways. Major Richard Christopher Clarke R.A.M.C. of No 19 CCS stated that during one offensive “The surgeons were to do sixteen-hour shifts with eight hours off, thus giving us four tables going day and night.” Evacuation Section: After an operation, the patient could be carried here to await evacuation back to a Base Hospital. As stated above, slightly wounded were sent here after their wounds were dressed. Retention ward: If the patient was too ill to be evacuated, he was taken to a retention ward. These were situated at the back of the CCS in as quiet a place as possible. He was attended to here by the nurses and medical officers. Major Clarke provides a good insight into how the CCS’s procedure worked “The commanding officer was to be responsible for the administration and evacuation, and I was responsible for every case until operated on or marked for immediate evacuation.... In the theatre we had six tables, and the anaesthetist started the next case while the surgeon was dressing the last. Each surgeon had a sister and one trained orderly, and there was a free N.C.O and a free sister in the theatre to do sterilizing of instruments, etc. When it is realized that by this system no surgeon saw the case he was to operate on until he was under the anaesthetic, the proper selection of cases was of the utmost importance, and that is why we arranged that one man, myself, should stand the racket of any mistake. For this purpose in the dressing-room I had twelve tables to fit stretchers and twelve orderlies, one to each table, and a most efficient corporal in charge. Every case was brought in, put on the table, his wounds undone and a decision made, by me, as to his disposal, either to the resuscitation ward, to the pre-operation ward, to a ward especially kept for the dying, straight to one of the surgical wards or for immediate evacuation. My problem in a battle was to keep all the surgeons busy with cases really urgently needing operation. At the same time I had not to send so many to the pre-operating room that the last case would have to wait longer for his operation than if sent to the base; and, above all, not to send cases in for operation so badly wounded as to be unlikely to recover. It was a fairly difficult business, but by being kept informed of train times, by interviewing ambulance drivers and finding if more were to come, and being in and out of the pre-operation room and theatre, I was able to get a fair idea of the position.” [The Evolution of A Casualty Clearing Station on the Western Front - the presidential address, delivered on 14th October 1936, at the opening of the sixty-fourth session of the Bristol Medico-Chirurgical society.] Equipment: In 1914, there were no definite regulations limiting the amount of material and tentage which could be added to CCSs. Individual commanding officers requisitioned for whatever equipment they might consider necessary. However, it was recommended that every CCS have tents to accommodate 200 patients, 210 stretchers, 200 Paillasse cases, 200 bolster cases, 480 sheets, 50 feather pillows, 400 blankets, along with sufficient cooking and feeding utensils, medical stores and comforts, and surgical equipment. Surgical equipment comprised of: 1 small operating tent, 1 operating table, a few wooden splints, and a few yards of aluminum splinting. Doctors were encouraged to use local resources to obtain what they required. In June 1915, a further increase of equipment was authorized and CCSs were supplied with the ‘Bowlby Outfit No 2’. Later in the war small operating tents/areas were replaced by a Nissan hut of 60 feet in length and 20 feet in width - room for 4 operating tables and their equipment. Due to the vast expansion of CCSs, it became necessary to regulate the quantity of equipment allocated. The new scale equipment was issued in routine orders. Sets of equipment were kept in reserve at the Base Depot of Medical Stores in Boulogne and was sent up when required. This equipment list is far too large to state here but can be found in Volume II of the Medical Services General Official History and Volume I of the Medical Services Surgery of the War. Transport: There was no scale for transport laid down for the units in 1914 mobilization tables, but a footnote explained that if transport was required it would be furnished under the orders of the Inspector-General of communications. It was advised they should receive 17 general service wagons and 8 or 9 3-ton motor lorries when the unit was on the move. However, after they had expanded it was documented that as many as 100, or even in one case 200, lorry loads or a complete train of goods vans had been used.

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Many organizations are moving toward cloud-based services and infrastructure as to provide on-demand services. Many enterprises now use cloud-based computing platforms that allow services and data to be accessed over the Internet (or via other networks). Infrastructure providers of these cloud-based computing platforms offer network-based processing systems that often support multiple enterprises (or tenants) using common computer hardware and data storage. This “cloud” computing model allows applications to be provided over the network “as a service” supplied by the infrastructure provider. The infrastructure provider typically abstracts the underlying hardware and other resources used to deliver an enterprise-developed application so that the enterprise no longer needs to operate and support dedicated server hardware. The cloud computing model can often deliver substantial cost savings to the enterprise over the life of the application because the enterprise no longer needs to provide dedicated network infrastructure, electrical and temperature controls, physical security and other logistics in support of dedicated server hardware. A data center is a facility that centralizes an organization's IT operations and equipment, and where it stores, manages, and disseminates its data. A data center includes equipment, such as servers for IT operations and storage hardware for storage of an organization's data. Detecting failures of equipment that is used in such data centers is important to help ensure reliability. Cloud applications increasingly depend on large volumes of data, which requires multiple tiers of storage. Multiple tiers of storage can differ in terms of their cost, capacity, latency, reliability, and power consumption characteristics. These tiers can include memory, flash memory, single disk storage, redundant array of independent disks (RAID) based storage, network-attached storage (NAS) devices, and storage area networks (SAN). RAID storage is a data storage technology that provides a way of storing the same data redundantly in different places on multiple storage devices. These storage devices are typically hard disk drive storage devices or in some cases solid-state storage devices (SSDs). RAID storage can provide fault tolerance by combining multiple storage devices into a single logical unit, or array, so that data can be mirrored at each of the storage devices in the same array. This way, if one storage device fails the data is still preserved. RAID storage can also help improve overall performance, and increase storage capacity in a system. In a typical data center, RAID-based storage systems are indispensable due to their lower cost and higher volume.

3.125

3

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Hydrogen is supplied to customers connected to a hydrogen pipeline system. Typically, the hydrogen is manufactured by steam methane reforming in which a hydrocarbon and steam are reacted at high temperature in order to produce a synthesis gas containing hydrogen and carbon monoxide. Hydrogen is separated from the synthesis gas to produce a hydrogen product stream that is introduced into the pipeline system for distribution to customers that are connected to the pipeline system. Alternatively, hydrogen produced from the partial oxidation of a hydrocarbon can be recovered from a hydrogen rich stream. Typically, hydrogen is supplied to customers under agreements that require availability and on stream times for the steam methane reformer or hydrogen recovery plant. When a steam methane reformer is taken off-line for unplanned or extended maintenance, the result could be a violation of such agreements. Additionally, there are instances in which customer demand can exceed hydrogen production capacity of existing plants. Having a storage facility to supply back-up hydrogen to the pipeline supply is therefore desirable in connection with hydrogen pipeline operations. Considering that hydrogen production plants on average have production capacities that are roughly 50 million standard cubic feet per day or greater, a storage facility for hydrogen that would allow a plant to be taken off-line, to be effective, would need to have storage capacity in the order of 1 billion standard cubic feet or greater. The large storage capacity can be met by means of salt caverns to store the hydrogen underground. Low purity grades of hydrogen (i.e., below 95% purity) as well as other gases have been stored in salt caverns. Salt caverns are large underground voids that are formed by adding fresh water to the underground salt, thus creating brine, which is often referred to as solution mining. Caverns are common in the gulf states of the United States where demand for hydrogen is particularly high. Such hydrogen storage has taken place where there are no purity requirements or less stringent (<96% pure) requirements placed upon the hydrogen product. In such case, the stored hydrogen from the salt cavern is simply removed from the salt cavern without further processing. High purity (e.g., 99.99%) hydrogen storage within salt caverns presents several challenges. For example, storing large quantities (e.g., greater than 100 million standard cubic feet) of pure (e.g., 99.99%) gaseous hydrogen in underground salt caverns consisting of a minimum salt purity of 75% halite (NaCl) or greater without measurable losses of the stored hydrogen is difficult based on the properties of hydrogen. Hydrogen is the smallest and lightest element within the periodic table of elements, having an atomic radius measuring 25 pm+/−5 pm. Further, hydrogen is flammable, and therefore a very dangerous chemical if not handled properly. Salt caverns consist of salt walls that have various ranges of permeability (e.g., 0-23×10^-6 Darcy) that if not controlled properly could easily allow gaseous hydrogen to permeate through the salt walls and escape to the surface of the formation. If the stored hydrogen within an underground salt formation was to escape and permeate through the salt formation to the surface, a dangerous situation could arise with fatality potential or immense structural damage potential. Consequently, high purity hydrogen is typically considered one of the most difficult elements to contain within underground salt formations. As will be discussed, among other advantages of the present invention, an improved method and system for storing hydrogen in a salt cavern is disclosed.

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This image was degraded by the researchers to show what the old telescope would have seen. Credit: Big Bear Solar Observatory NJIT's new 1.6-meter clear aperture solar telescope—the largest of its kind in the world—is now operational. The unveiling of this remarkable instrument—said to be the pathfinder for all future, large ground-based telescopes—could not have come at a more auspicious moment for science. This year marks the 400th anniversary of Galileo's telescope that he used to demonstrate that sunspots are indeed on the Sun. "With our new big, beautiful white machine, Galileo's work can leap ahead with a capability never before available," said NJIT distinguished professor of physics Philip R. Goode. Goode, the heart and soul of the project, has been director of Big Bear Solar Observatory (BBSO), since NJIT took over management of BBSO in 1997 from California Institute of Technology. Located high above sea level in Big Bear Lake, CA, the observatory is one of six major land-based facilities supported by federal funding. This photo is the first light image from the new solar telescope at Big Bear Solar Observatory. Credit: Big Bear Solar Observatory "We are already seeing photos offering a better understanding of the Sun," said Goode. "With this instrument we should be able to have a better understanding of dynamic storms and space weather—which can have dramatic effects on Earth." Earlier this month, researchers achieved what is called first scientific light. This means the telescope is finally operational. To achieve its full powers, at least three more years of work will be needed. Photos from the first observations are still being processed. Nevertheless, Goode and his researchers were able to extract a few unique images and one is shown here. It clearly illustrates the before-and-after capabilities of the old versus new telescope. "Our prized first image shows the Sun's ever-present, turbulent granular field with its largest granules being about the size of Alaska," Goode said. "The small, bright points in the dark lanes are the smallest-scale magnetic structures on the Sun. Look closely at the "after" photo (which you may want to enlarge) and you will see a string of pearls. Each pearl is a cross-section of an intense, single fiber of the Sun's magnetic field - the basic building block of the solar magnetism." Goode adds that the Sun is now in a state of prolonged magnetic inactivity, perhaps the longest such time in a century. "The new telescope is ideal for studying the Sun as it rises from this strange state of quietude," he added. The new instrument has three times the aperture of the old telescope. It represents a significant advance in high-resolution observations of the Sun, since it has the largest aperture of any solar telescope in existence, said Goode. Other pluses include a marvelous location-- high in a Southern California mountain lake, and since it is an off-axis instrument, there is no part of sunlight blocked by the telescope, itself. The new telescope will be used in joint observation campaigns with NASA satellites to optimize the scientific output of all observations of the Sun. BBSO has always operated in such campaigns, but now can do so with greatly-enhanced capabilities. The National Science Foundation (NSF), Air Force Office of Special Research (AFOSR) and NASA have provided more than $5 million in hardware components. The telescope is filled with new technologies. The 1.7-meter (equivalent to 4.6 feet) primary mirror was polished by the world-renowned Steward Observatory Mirror Laboratory at the University of Arizona (UA). The extremely-precise measurements of the mirror's shape required the application, for the first time, of a computer-generated hologram. The development of this technology will be essential for figuring the next generation of even-larger night time telescopes. The final error in the primary mirror is only a few parts in a billion from its desired parabolic shape. "Buddy Martin at the UA Mirror Lab has described the mirror in ours as the pathfinder for large nighttime telescopes that are about-to-be built," said Goode. This is the new solar telescope at Big Bear Solar Observatory. Credit: Big Bear Solar Observatory Another key design issue for this large-aperture solar telescope was the creation of a thermal control system capable of maintaining the temperature of the mirrors near or below ambient air. To achieve this, the dome employs a wind-gate and exhaust system which controls the airflow from the wind. The structure maintains the same temperature inside and outside the dome, and clears concentrations of heat in and around the optical paths. In addition, BBSO engineers implemented a closed-cycle, chilled-air system as part of the telescope mount to limit so-called "mirror seeing." This sweeps away turbulent cells and directly cools the primary mirror. After a day of observations, the mirror must be cooled overnight to ensure that it is somewhat cooler than ambient in the morning. DFM Engineering, Longmont, CO, built and tested the optical support structure and active-support mirror cell for the enormous mirror. It is supported by 36 actuators that can bend out low-order aberrations, such as those due to gravity and/or thermal effects. The telescope is now in its commissioning phase in which more sophisticated observations are made possible with the implementation of advanced hardware. These include adaptive optics to correct for atmospheric distortion and hardware to measure magnetic fields in visible and infrared light. "It is good at last to have our destiny in our own hands rather than those of our capable partners," said Goode. "Seeing first light was a great moment because the team in BBSO finally knew that its big white machine works as we had planned." Source: New Jersey Institute of Technology Explore further NJIT physicists expect new super lens to reveal first light by early 2006

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Introduction {#sec1} ============ Since December 2019, several cases of pneumonia of unknown etiology have been reported in Wuhan, Hubei Province, of China.[@bib1] Those cases have been confirmed as acute respiratory infections caused by a novel coronavirus infection. To date, confirmed cases have been found in many countries worldwide.[@bib2] ^,^ [@bib3] Until now, however, the source of the virus and the pathogenesis of the disease are unknown. Early detection, quarantine, and timely treatment are the keys to better controlling the epidemic and reducing the spread of the disease. Coronaviruses are RNA viruses and can be divided into 4 genera according to the genomic characteristics: α, β, γ, and ξ.[@bib4] Among these, Middle East respiratory syndrome coronavirus and severe acute respiratory syndrome coronavirus are known coronaviruses.[@bib4] ^,^ [@bib5] The new virus recently discovered in China is now recognized to be a novel coronavirus named 2019-nCoV. The coronavirus isolated from patients with this novel pneumonia in Wuhan is a coronavirus of genus β.[@bib5] This sudden infectious disease mainly manifests as fever, fatigue, and cough.[@bib6], [@bib7], [@bib8] Upper respiratory symptoms such as nasal congestion and runny nose are rare. About one half of the patients develop dyspnea after 1 week.[@bib9] In severe cases, patients progress rapidly to acute respiratory distress syndrome (ARDS), sepsis, and coagulopathy. Some patients have mild symptoms with no fever or without pneumonia and usually recover after 1 week. However, some patients may suddenly worsen and develop ARDS.[@bib9] At present, how to stratify high-risk and low-risk patients is an important but unresolved issue. In the present study, the clinical manifestations and clinical outcomes of patients with 2019 novel coronavirus disease (COVID-19) were evaluated. The purpose of this study was to identify the risk factors associated with pneumonia, ARDS, and clinical outcomes. Patients and methods {#sec2} ==================== Patients {#sec2.1} -------- This cross-sectional multicenter clinical study was approved by the institutional ethics board of the Nanfang Hospital, Southern Medical University. All consecutive patients with confirmed 2019-nCoV infections who were diagnosed in the Dongguan People\'s Hospital and Nanfang Hospital, Southern Medical University, from January 2020 to February 2020 were enrolled. The study population comprised hospitalized patients. Because COVID-19 is an infectious disease, all outpatients were required to be quarantined in the hospital if infection with 2019-nCoV was confirmed. The 2019-nCoV infection diagnostic standard was polymerase chain reaction detection of 2 target genes of 2019-nCoV, open reading frame 1 ab (ORF1ab) and nucleocapsid protein. A positive result was determined to be 2019-nCoV infection. Ethics, Consent, and Permissions {#sec2.2} -------------------------------- The Institutional Review Board of Nanfang Hospital, Southern Medical University, approved this study. All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation and with the 1975 Declaration of Helsinki as revised in 2008. Oral consent was obtained from patients. Data Collection {#sec2.3} --------------- All patients\' clinical, laboratory, and radiologic characteristics, as well as treatment outcome data, were obtained through medical record extraction. Data were reviewed by a team of trained physicians. The recorded information included demographic data, medical history, contact history, potential comorbidities, symptoms, laboratory test results, and chest computed tomography (CT) scans. ARDS was defined as an acute-onset oxygenation index (arterial partial pressure of oxygen/fraction of inspired oxygen) ≤ 300 mm Hg and a chest radiograph showing patchy shadows.[@bib10] Real-Time Polymerase Chain Reaction Assay for 2019-nCoV {#sec2.4} ------------------------------------------------------- All patients had pharyngeal swab samples collected to detect 2019-nCoV. The specific steps were as follows: The throat swab was placed into a collection tube containing 150 μL of virus preservation solution, and a respiratory sample RNA isolation kit (Zhongzhi, Wuhan, China) was used to extract total RNA within 2 h. Forty microliters of cell lysate were transferred to a collection tube and vortexed for 10 s. It was centrifuged after incubation at room temperature for 10 min. Real-time polymerase chain reaction was then performed, and 2 target genes (ORF1ab and nucleocapsid protein) were detected. Target 1 (ORF1ab): forward primer CCTGGTGGGTTTTACACTTAA; reverse primer ACGATTGTGCATCAGCTGA; probe 5′-VIC-CCGTCTGCGGTATGTGGAAAGGTTATGG-BHQ1-3′. Target 2 (N protein): forward primer GGGGAACTTCTCCTGCTAGAAT; reverse primer CAGACATTTTGCTCTCAAGCTG; probe 5′-FAM-TTGCTGCTGCTTGACAGATT-TAMRA-3′. The diagnostic criteria were based on the recommendations of the National Institute of Viral Disease Prevention and Control (<http://ivdc.chinacdc.cn/kyjz/202001/t20200121_211337.html>). Statistical Analysis {#sec2.5} -------------------- Continuous data are reported as mean (SD), and categorical data are expressed as percentages. The significance of differences was tested by using either the Student\'s *t* test (for continuous variables) or the χ2 test (for categorical variables). Univariable and multivariable regression analyses were performed by using logistic regression analysis, and the results are expressed as odds ratio (OR) and 95% CIs. All analyses were performed by using SPSS version 13.0 (IBM SPSS Statistics, IBM Corporation, Armonk, New York) with an alpha level of 0.05. Results {#sec3} ======= Characteristics of Patients With COVID-19 {#sec3.1} ----------------------------------------- A total of 95 patients infected with 2019-nCoV were enrolled. Seventy-three had pneumonia based on the CT findings, and 22 did not have pneumonia. Demographic and clinical characteristics are shown in [Table I](#tbl1){ref-type="table"} . Patients with pneumonia were significantly older than the other patients (*p* \< 0.001). The body mass index (BMI) (*p* = 0.001), aspartate aminotransferase levels (*p* = 0.041), and lactate dehydrogenase (LDH) levels (*p* = 0.003) were significantly higher in patients with pneumonia. However, lymphocyte count (*p* = 0.014) and platelet count (*p* \< 0.001) were significantly lower in patients with pneumonia.Table IDemographic and clinical characteristics in patients with coronavirus disease 2019 (COVID-19) with or without pneumonia. Values are givens as mean (SD) unless otherwise indicated.Table ICharacteristicPatients With COVID-19*P*With PneumoniaWithout PneumoniaSample size, n7322--Male sex39 (53.4%)14 (63.6%)0.398Age, y42.66 (17.93)23.86 (13.88)\<0.001SBP, mm Hg126.41 (16.01)120.95 (14.90)0.175DBP, mm Hg83.69 (10.26)79.90 (8.60)0.138BMI, kg/m^2^23.71 (3.41)20.78 (3.15)0.001Serum lactic acid, mmol/L1.51 (0.71)1.61 (0.59)0.608Neutrophil count, × 10^9^3.32 (1.52)3.33 (1.29)0.972Lymphocyte count, × 10^9^1.25 (0.94)1.81 (0.87)0.014Hemoglobin, g/L139.07 (18.07)143.41 (13.01)0.298Platelet count, × 10^9^196.27 (56.67)251.50 (77.46)\<0.001Serum creatinine, μmol/L68.60 (41.11)60.95 (17.97)0.400ALT, U/L21.33 (12.00)22.77 (24.75)0.718AST, U/L23.97 (10.48)18.75 (7.72)0.041LDH, IU/L204.04 (67.44)154.32 (34.88)0.003Tobacco smoking5 (6.8%)3 (13.6%)0.315[^2] Univariate and Multivariate Analyses of Factors Associated With Pneumonia {#sec3.2} ------------------------------------------------------------------------- Univariate and multivariate analyses were conducted to analyze the risk factors associated with 2019-nCoV--infected patients developing pneumonia. Univariate results showed that older age, high BMI, low lymphocyte count, low platelet count, high aspartate aminotransferase level, and high LDH level were risk factors associated with patients developing pneumonia. However, multivariate analysis showed that only older age (OR, 1.078; *p* = 0.008) and high BMI (OR, 1.327; *p* = 0.024) were independent risk factors associated with patients developing pneumonia ([Table II](#tbl2){ref-type="table"} ).Table IIFactors associated with pneumonia in patients with coronavirus disease 2019.Table IIVariableUnivariate AnalysisMultivariate AnalysisOR95% CI*P*OR95% CI*P*Sex0.6550.245--1.7510.400Age1.0731.034--1.112\<0.0011.0781.020--1.1400.008SBP1.0230.990--1.0570.176DBP1.0400.987--1.0950.141BMI1.2981.103--1.5270.0021.3271.038--1.6970.024Serum lactic acid0.8150.376--1.7650.603Neutrophil count0.9940.717--1.3780.972Lymphocyte count0.5480.305--0.9860.045Hemoglobin0.9860.959--1.0130.301Platelet count0.9870.979--0.9950.002Serum creatinine1.0110.986--1.0360.387ALT0.9940.965--1.0250.716AST1.0801.001--1.1650.048LDH1.0231.007--1.0390.004Tobacco smoking0.4660.102--2.1270.324[^3] Differences in Characteristics Between the ARDS Group and the Non-ARDS Group {#sec3.3} ---------------------------------------------------------------------------- Using the ARDS definition, patients were divided into an ARDS group (*n* = 24) and a non-ARDS group (*n* = 71) ([Table III](#tbl3){ref-type="table"} ). Patients with ARDS were older than those without ARDS (*p* = 0.021). Moreover, systolic blood pressure (SBP) (*p* = 0.038), serum creatinine (*p* = 0.025), and LDH (*p* = 0.003) levels were significantly higher in patients with ARDS. However, lymphocyte counts were lower in patients with ARDS than in others (*p* = 0.046).Table IIIThe demographic and clinical characteristics in patients with coronavirus disease 2019 (COVID-19) with and without acute respiratory distress syndrome (ARDS). Values are given as mean (SD) unless otherwise indicated.Table IIICharacteristicPatients With COVID-19*P*With ARDSWithout ARDSSample size, n2471--Male sex14 (58.3%)39 (54.9%)0.772Age, y45.92 (18.44)35.73 (13.32)0.021SBP, mm Hg130.96 (14.62)123.15 (15.87)0.038DBP, mm Hg84.92 (10.42)82.12 (9.93)0.245BMI, kg/m^2^24.26 (3.32)22.64 (3.55)0.053Serum lactic acid, mmol/L1.49 (0.51)1.55 (0.74)0.703Neutrophil count, × 10^9^3.21 (1.34)3.36 (1.51)0.656Lymphocyte count, × 10^9^1.05 (0.48)1.49 (1.04)0.046Hemoglobin, g/L141.46 (12.47)139.61 (18.41)0.648Platelet count, × 10^9^193.67 (67.23)214.27 (65.15)0.187Serum creatinine, μmol/L81.42 (65.91)61.90 (18.02)0.025ALT, U/L23.83 (14.07)20.91 (16.05)0.439AST, U/L25.49 (11.68)21.92 (9.48)0.146LDH, IU/L228.86 (80.21)181.79 (55.17)0.003Tobacco smoking1 (4.2%)7 (9.9%)0.385[^4] Univariate and Multivariate Analyses of Factors Associated With ARDS {#sec3.4} -------------------------------------------------------------------- Logistic regression was used to identify factors that were significantly associated with ARDS in patients with COVID-19. In multivariate analysis, high SBP level (OR, 1.046; *p* = 0.025) and high LDH level (OR, 1.010; *p* = 0.021) were found to be independent risk factors associated with ARDS among patients with COVID-19 ([Table IV](#tbl4){ref-type="table"} ).Table IVFactors associated with acute respiratory distress syndrome in patients with coronavirus disease 2019.Table IVVariableUnivariate AnalysisMultivariate AnalysisOR95% CI*P*OR95% CI*P*Sex1.1490.450--2.9300.772Age1.0311.004--1.0580.025SBP1.0331.001--1.0660.0421.0461.006--1.0890.025DBP1.0290.981--1.0790.244BMI1.1470.996--1.3200.057Serum lactic acid0.8650.416--1.8010.699Neutrophil count0.9270.665--1.2920.652Lymphocyte count0.3590.141--0.9180.032Hemoglobin1.0060.980--1.0340.645Platelet count0.9950.987--1.0030.188Serum creatinine1.0210.995--1.0480.116ALT1.0110.983--1.0400.443AST1.0330.988--1.0800.154LDH1.0111.003--1.0180.0071.0101.001--1.0190.021Tobacco smoker0.3980.046--3.4080.400[^5] Differences in Characteristics Between Patients With Pneumonia Exacerbation and Relief {#sec3.5} -------------------------------------------------------------------------------------- A total of 70 patients underwent CT scanning repeatedly after 1 week of treatment. Based on the findings obtained after comparison with the first CT scan, patients were divided into the pneumonia exacerbation group (*n* = 19) and the pneumonia relief group (*n* = 51). The characteristics were compared, and the results showed that patients with pneumonia exacerbation were significantly older (*p* = 0.021), with a higher BMI (*p* = 0.003) and a higher proportion of tobacco smokers (*p* = 0.006) ([Table V](#tbl5){ref-type="table"} ).Table VDemographic and clinical characteristics in patients with coronavirus disease 2019 (**COVID-19) with pneumonia exacerbation or relief.**Table VCharacteristicPatients with COVID-19*P*Pneumonia ExacerbationPneumonia ReliefSample size, n1951--Male sex11 (57.9%)24 (47.1%)0.420Age, y49.58 (22.16)38.37 (15.80)0.021SBP, mm Hg127.63 (13.11)125.39 (17.43)0.614DBP, mm Hg81.26 (10.95)84.14 (10.58)0.322BMI, kg/m^2^25.38 (2.49)22.95 (3.61)0.003Serum lactic acid, mmol/L1.53 (0.75)1.56 (0.72)0.896Neutrophil count, × 10^9^3.47 (1.62)3.29 (1.58)0.679Lymphocyte count, × 10^9^1.13 (0.58)1.31 (1.05)0.481Hemoglobin, g/L139.68 (13.46)137.92 (19.83)0.722Platelet count, × 10^9^184.95 (50.78)207.19 (60.51)0.159Serum creatinine, μmol/L81.74 (73.92)61.76 (17.34)0.073ALT, U/L19.38 (11.03)21.78 (12.55)0.477AST, U/L23.26 (12.71)23.80 (10.05)0.856LDH, IU/L201.16 (80.15)200.40 (64.92)0.968Tobacco smoking4 (21.1%)1 (2.0%)0.006[^6] Univariate and Multivariate Analyses of Factors Associated With Pneumonia Exacerbation {#sec3.6} -------------------------------------------------------------------------------------- Logistic regression was used to identify factors that were associated with pneumonia exacerbation in patients with COVID-19. Multivariate analysis showed that a high BMI (OR, 1.285; *p* = 0.017) and tobacco smoking (OR, 16.13; *p* = 0.032) were independent risk factors associated with 2019-nCoV--infected patients with pneumonia exacerbation after treatment ([Table VI](#tbl6){ref-type="table"} ).Table VIFactors associated with pneumonia exacerbation in patients with coronavirus disease 2019.Table VIVariableUnivariate AnalysisMultivariate AnalysisOR95% CI*P*OR95% CI*P*Sex1.5470.534--4.4820.422Age1.0371.004--1.0710.026SBP1.0090.976--1.0420.608DBP0.9740.926--1.0250.319BMI1.2531.049--1.4970.0131.2851.045--1.5810.017Serum lactic acid0.9490.440--2.0470.894Neutrophil count1.0720.774--1.4850.674Lymphocyte count0.7460.325--1.7140.490Hemoglobin1.0050.977--1.0340.718Platelet count0.9930.983--1.0030.161Serum creatinine1.0140.990--1.0390.244ALT0.9820.936--1.0310.472AST0.9950.945--1.0480.854LDH1.0000.992--1.0080.967Tobacco smoking6.6671.110--40.040.03816.131.275--204.160.032[^7] Discussion {#sec4} ========== The present study found that older age and high BMI were independent risk factors associated with patients with pneumonia. Furthermore, high SBP level and high LDH level were independent risk factors associated with ARDS among patients with COVID-19. High BMI and tobacco smoking were independent risk factors associated with pneumonia exacerbation after treatment in patients with COVID-19. These results help in the risk stratification of patients with COVID-19. Timely intervention should be initiated in patients with risk factors to avoid disease progression. In addition, the results of this study may have implications for the pathogenesis of COVID-19. Most patients with COVID-19 will develop pneumonia.[@bib11] However, a small proportion of patients have negative radiographic findings. The largest study sample to date showed that among the 3665 confirmed cases, 95.5% (*n* = 3498) of patients were diagnosed with pneumonia.[@bib12] According to the Diagnosis and Treatment Program of 2019 New Coronavirus Pneumonia recommended by The National Health Commission of China, these patients only exhibited low fever and mild fatigue with no pneumonia manifestations, and they usually recovered after 1 week. Our study confirmed these results. We found that some patients had negative CT scan results, although the throat swabs confirmed infection with 2019-nCoV. Most previous studies were conducted in Wuhan Province with patients enrolled from Wuhan, and the symptoms of those first-generation patients were relatively severe. The patients enrolled in the present study were from Guangdong Province, which is not the first generation of infected patients. In our study, the patients' symptoms were relatively mild, which is in line with the results of patients from Zhejiang Province.[@bib13] Symptoms of patients outside Hubei Province are relatively mild. Some 2019-nCoV--infected patients will rapidly become critically ill.[@bib9] ^,^ [@bib14] Previous research reported that the mortality rate of 2019-nCoV--infected patients is 4%--15%.[@bib7] ^,^ [@bib9] In our study, only one patient aged 75 years (BMI, 29.37 kg/m^2^) died (mortality rate, 1.05%). Therefore, early detection of this population is very important. However, this subpopulation of patients who have severe disease may have moderate to low fever in the development of the disease. It is still difficult to screen out these patients. Our research may provide a sign. According to the results of our study, the 2019-nCoV--infected patients who developed ARDS were older and had higher SBP, serum creatinine, and LDH levels. This group of people also had lower lymphocyte counts. However, multivariate analysis suggested that only high SBP level and high LDH level were independent risk factors associated with ARDS among patients with COVID-19. Previous research implied that some patients' conditions will change dramatically in \~1 week.[@bib9] In our study, we performed repeated CT examinations on 70 patients after 1 week of treatment and found that those with imaging findings suggesting exacerbations had clinical baseline data significantly different from patients with reduced disease. Tobacco smoking has been confirmed to be associated with many diseases.[@bib15] ^,^ [@bib16] In our study, multivariate analysis suggests that high BMI and tobacco smoking were independent risk factors associated with disease exacerbation in 2019-nCoV--infected patients after treatment. Until now, there have been no antiviral drugs specifically approved for treating 2019-nCoV--infected patients. Although reports have suggested the potential antiviral effects of lopinavir/ritonavir, it remains controversial.[@bib14] Remdesivir has shown strong potential antiviral effects in previous reports but has not yet been approved by the US Food and Drug Administration, and large clinical research results are lacking to support its application.[@bib2] ^,^ [@bib17] Finding an effective treatment plan is a particularly important clinical problem. The present study discusses the evolution of CT findings for patients with COVID-19. However, CT scans are not frequently used for assessment of patients with complicated pneumonia or ARDS. CT scan findings cannot completely identify exacerbation or relief of the disease. The CT scan results can only reflect some aspects in the development of the disease. The findings from our study may not have clinical relevance across different parts of the world. This study has limitations. First, it involved a cross-sectional investigation. Second, the relative sample size was limited. The potential limitations of the present report could be overcome in future studies by enrolling more patients. In our study, there was no control group, and there was no comparator virus-infected group. Most of these findings are the same as would be seen with influenza, respiratory syncytial virus, and human metapneumovirus. The results from our study may imply that high-risk patients are at high risk of complications because of who they are (their specific characteristics), and not because of the specific nature of the individual pathogen. The airway inflammation coupled with their clinical factors is the real issue. In addition, prognostic outcomes were assessed. In the present study, all patients diagnosed with ARDS were admitted to the intensive care unit to continue further treatment. However, other prognostic outcomes, including length of stay data, in this study are missing because some patients are still in the hospital. Further study is needed to determine mortality and length of stay data. Conclusions {#sec5} =========== Older age and high BMI were independent risk factors associated with pneumonia in patients with COVID-19. High SBP and LDH levels were independent risk factors associated with ARDS, whereas high BMI and tobacco smoking were independent risk factors associated with disease exacerbation after treatment. For such patients, stratification by using independent risk factors could help with the management of their disease. Disclosures =========== The authors have indicated that they have no conflicts of interest regarding the content of this article. This work was supported by grants from the 10.13039/501100013076Major Science and Technology Special Project of China (2017ZX09304016, 2017ZX10302201004008). The authors thank Jian Zhang for his helpful assistance in the study. Drs. S. Cai, Yin, Xu, and Peng designed and guided the study; Drs. S. Cai and Yu wrote the main manuscript text; and Drs. Zheng, Liu, and X. Cai prepared all tables and data analysis. All authors reviewed the manuscript. [^1]: These authors contributed equally to this work. [^2]: ALT = alanine aminotransferase; AST = aspartate aminotransferase; BMI = body mass index; DBP = diastolic blood pressure; LDH = lactate dehydrogenase; SBP = systolic blood pressure. [^3]: ALT = alanine aminotransferase; AST = aspartate aminotransferase; BMI = body mass index; DBP = diastolic blood pressure; LDH = lactate dehydrogenase; OR = odds ratio; SBP = systolic blood pressure. [^4]: ALT = alanine aminotransferase; AST = aspartate aminotransferase; BMI = body mass index; DBP = diastolic blood pressure; LDH = lactate dehydrogenase; SBP = systolic blood pressure. [^5]: ALT = alanine aminotransferase; AST = aspartate aminotransferase; BMI = body mass index; DBP = diastolic blood pressure; LDH = lactate dehydrogenase; OR = odds ratio; SBP = systolic blood pressure. [^6]: ALT = alanine aminotransferase; AST = aspartate aminotransferase; BMI = body mass index; DBP = diastolic blood pressure; LDH = lactate dehydrogenase; SBP = systolic blood pressure. [^7]: ALT = alanine aminotransferase; AST = aspartate aminotransferase; BMI = body mass index; DBP = diastolic blood pressure; LDH = lactate dehydrogenase; OR = odds ratio; SBP = systolic blood pressure.

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Reducing Risks to Women Linked to Shift Work, Long Work Hours, and Related Workplace Sleep and Fatigue Issues. In the United States, an estimated 12% to 28% of working women are on shift work schedules, and 12% work more than 48 hours per week. Shift work and long work hours are associated with many health and safety risks, including obesity, injuries, and negative reproductive outcomes. Over time, the worker is at risk for developing a wide range of chronic diseases. These work schedules can also strain personal relationships, owing to fatigue and poor mood from sleep deprivation and reduced quality time to spend with family and friends. Worker errors from fatigue can lead to reduced quality of goods and services, negatively impacting the employer. In addition, mistakes by fatigued workers can have far-reaching negative effects on the community, ranging from medical care errors to motor vehicle crashes and industrial disasters that endanger others. To reduce the many risks that are linked to these demanding work hours, the National Institute for Occupational Safety and Health (NIOSH) conducts research, develops guidance and authoritative recommendations, and translates and disseminates scientific information to protect workers, their families, employers, and the community. The key message to reduce these risks is making sleep a priority in the employer's systems for organizing work and in the worker's personal life. The NIOSH website has freely available online training programs with suggestions for workers and their managers to help them better cope with this workplace hazard.

3.078125

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Hydrated alkali metal silicates are known fire-proofing materials and are extensively employed in building construction. Under the high temperatures existing during a fire, the water of hydration is driven off causing the composition to puff, expanding by up to 25 to 40 times its original volume. Thus, when combined with fire-stop materials these materials intumesce to provide a layer of insulation against fire and smoke, said layer being full of bubbles and holes from the expansion of the water of hydration. The foaming pressure helps to seal apertures and passages in building structures making these fireproofing materials useful in fire-stops, see U.S. Pat. No. 4,364,210. Alkali metal silicates can also be incorporated into proofing materials such as asphalt shingles in order to convert these shingles into a fire retardant Class A or B form. Alkali metal silicate particles may be placed in an asphalt layer in between the top layer of asphalt and roofing granules and the substrate of organic felt or fiberglass mat. In the event of a fire on a roof, the intumescent silicate particles expand to form a thermal barrier which retards ignition of the roofing deck. The formation of alkali metal silicate gels by the addition of such materials as sodium aluminate or boric acid solutions to alkali metal silicates at elevated temperatures is known (see U.S. Pat. No. 4,297,252, Example 3, and U.S. Pat. No. 3,498,807, column 3, lines 42-56). It is also known that the production of a solid, hydrated alkali metal silicate in which the moisture content is controlled can require carefully controlled drying conditions (see U.S. Pat. No. 3,895,995). Typically, alkali metal silicate suspensions or gels described in the literature are dried or cured at temperatures ranging from 90.degree. to 136.degree. C. and below the boiling point of the suspension or solution. One difficulty with silicate based materials is their degradation on exposure to water or high relative humidity for extended periods of time. Water is known to leach away the alkali metal oxide from the silicate particles, reducing their ability to intumesce. Various solutions to this problem have been proposed in the past, including a coating which covers alkali metal silicate particles (see U.S. Pat. No. 4,218,502). it is the object of this invention to provide an alkali metal silicate material which retains its intumescence after long exposure to water in order to ensure that its effectiveness as a fire protection agent will last a long time under outdoor weathering conditions.

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Northern Gully This Mars Global Surveyor (MGS) Mars Orbiter Camera (MOC) image shows a gully formed in the wall of a north middle-latitude crater. Similar gullies are common at the middle and polar latitudes of Mars, and might have formed by the action of liquid water. Others have argued for carbon dioxide or dry mass movement for the genesis of such landforms. This particular image was acquired during northern autumn, when the sky over the terrain of the martian northern mid-latitudes is typically hazy. MGS MOC Release No. MOC2-1234, 28 September 2005

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Primary Menu PCB Making: 2. Get Started This is a step of looking for an idea or the purpose of what a board should be doing. You will likely know what you need and then build a suitable board. I needed to build something useful so I can look forward to it once it was done: I wanted to be able to interact with it but also use parts that I already have at home. In my parts bin, I found a fairly standard LCD display that I got with an Arduino board. It can display 16 characters in 2 rows. This should be a good display device to use. A couple of push-buttons are definitely a must for any interactivity as well as a few LEDs: can’t do without mandatory blinking lights! Digging through my parts I’ve found a DS18B20 temperature sensor, a simple 1-Wire device, so I added it in. Bins with various parts I wanted to use the Atmel SAM3N1 CPU which I already ordered from DigiKey. This quite powerful MCU needs a JTAG to program it. The MCU has a number of built in peripherals including an UART (“serial port”) so I also wanted to use those pins to communicate through the serial interface. After adding needed parts in the power supply circuitry, pin headers, test pins and so on, I felt that was complex enough for the scope of this project. Bins and bags of parts The final rough idea for a board quickly took shape: it should have a couple of buttons for user interaction, it should display temperature read from a sensor and to make it more interesting, display a random fortune (do you remember that old ‘fortune’ Unix application?).

3

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Q: What is wrong with this code that calculates areas, please? (Python) Hello, I am new to python. And I do not know why this code does not work: def area_finder_rectangle (height,width): area = height*width print("The area of your polygon is %.2f" % area) def area_finder_triangle (height,width): area = (height*width)*0.5 print("The area of your polygon is %.2f" % area) while True: print ("Choose the polygon that you want to calculate the area from.") print ("Polygons supported: rectangle, triangle") value = str(input("Your polygon is a: ")) print ("Be sure to include decimals even if you are going to input an integer") if value == "rectangle" or "Rectangle": heightt = float(input("Enter height: ")) widthh = float(input("Enter width: ")) area_finder_rectangle (height = heightt,width = widthh) elif value == "triangle" or "Triangle": heightt = float(input("Enter height: ")) widthh = float(input("Enter width: ")) area_finder_triangle (height = heightt,width = widthh) print ("") When you choose rectangle is just fine, but when you choose triangle, this happens: >>> Choose the polygon that you want to calculate the area from. Polygons supported: rectangle, triangle Your polygon is a: triangle Be sure to include decimals even if you are going to input an integer Enter height: 10 Enter width: 10 The area of your polygon is 100.00 A: if value == "rectangle" or "Rectangle": is not what you think it is. It will compare value with the complete result of the expression "rectangle" or "Rectangle" which will always evaluate to True. It should be like this: if value == "rectangle" or value == "Rectangle": But a better option is if value.lower() == "rectangle": Or even better, convert to lowercase directly at the input. value = str(input("Your polygon is a: ")).lower() Sidenote: If you want to compare a value with several values, you can do like this: if value in ["rectangle", "Rectangle", "RECTANGLE"]: But in this case that's not an optimal option. Just convert to lowercase before comparing. Here is complete code: def area_finder_rectangle (height,width): area = height*width print("The area of your polygon is %.2f" % area) def area_finder_triangle (height,width): area = (height*width)*0.5 print("The area of your polygon is %.2f" % area) while True: print ("Choose the polygon that you want to calculate the area from.") print ("Polygons supported: rectangle, triangle") value = str(input("Your polygon is a: ")).lower() print ("Be sure to include decimals even if you are going to input an integer") if value == "rectangle": heightt = float(input("Enter height: ")) widthh = float(input("Enter width: ")) area_finder_rectangle (height = heightt,width = widthh) elif value == "triangle": heightt = float(input("Enter height: ")) widthh = float(input("Enter width: ")) area_finder_triangle (height = heightt,width = widthh) print ("") And a testrun: [klutt@klutt-sandbox tmp]# python3 polygon.py Choose the polygon that you want to calculate the area from. Polygons supported: rectangle, triangle Your polygon is a: rectangle Be sure to include decimals even if you are going to input an integer Enter height: 10.0 Enter width: 10.0 The area of your polygon is 100.00 Choose the polygon that you want to calculate the area from. Polygons supported: rectangle, triangle Your polygon is a: triangle Be sure to include decimals even if you are going to input an integer Enter height: 10.0 Enter width: 10.0 The area of your polygon is 50.00 One thing you should consider, which in this case would have made it easier for you to discover the problem, is to always add an else in case of non-valid input. if value == "rectangle": <do something> elif value == "triangle": <do something> else: print("Unknown polygon") A: Your branch if value == "rectangle" or "Rectangle:" will always be taken and you will always calculate a rectangle. Why it does this makes more sense if you put in parentheses. if (value == "rectangle") or ("Rectangle"): If value is 'triangle' the first part evaluates to False but the second part of the or-condition evaluates to True since in Python a non-empty string in a boolean context is considered True. To get the effect you want you need to say if (value == "rectangle") or (value == "Rectangle"):

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All relevant data are within the paper and its Supporting Information files. Introduction {#sec001} ============ The brain size of humans has increased dramatically during the evolution of *Homo sapiens*, along with the acquisition of uniquely human features, such as language, memory, self-awareness, creativity, and social communication \[[@pone.0179624.ref001]--[@pone.0179624.ref005]\]. Elucidating the similarities and differences in the ontogeny of brain structures between humans and our closest living primate relatives, chimpanzees, is important to understand the unique features of the human brain. The corpus callosum (CC) is the major commissural white matter bundle that connects the left and right cerebral hemispheres and provides interhemispheric integration, which is related to sensory, motor, and higher-order cognitive functions \[[@pone.0179624.ref006], [@pone.0179624.ref007]\]. The CC is present in all primates and has evolved with the neocortex \[[@pone.0179624.ref008], [@pone.0179624.ref009]\]. The CC exhibits a topographic pattern of the different cortical areas \[[@pone.0179624.ref007], [@pone.0179624.ref010], [@pone.0179624.ref011]\], which is associated with different regions: the rostrum; genu; rostral body; and the anterior midbody connect regions of the prefrontal and frontal cortex; the posterior midbody connects the region of the somatosensory cortex; the isthmus connects regions of the parietal and superior temporal cortex; and the splenium connects the occipital, inferior temporal, and parietal regions \[[@pone.0179624.ref012]--[@pone.0179624.ref017]\]. This topographic relationship is similar in humans and chimpanzees \[[@pone.0179624.ref018]\]. The midsagittal area of the CC has been commonly used as a sensitive marker of brain development and maturation \[[@pone.0179624.ref019]--[@pone.0179624.ref023]\], since the CC area is related to number of axons and morphology, such as axon diameter and myelination \[[@pone.0179624.ref024]--[@pone.0179624.ref028]\]. In humans, midsagittal CC areas increase rapidly during the first two to three years of life (corresponds to infancy: note that the anthropological definition \[[@pone.0179624.ref029]--[@pone.0179624.ref036]\], which is different from the medical definition, is adopted in this report. See the Section "Definitions of developmental stages" for details) \[[@pone.0179624.ref037], [@pone.0179624.ref038]\] and continue to increase slowly during the juvenile stage, adolescence \[[@pone.0179624.ref021]--[@pone.0179624.ref023], [@pone.0179624.ref038]--[@pone.0179624.ref040]\], and young adulthood, until the third decade of life \[[@pone.0179624.ref019], [@pone.0179624.ref021], [@pone.0179624.ref041], [@pone.0179624.ref042]\]. In chimpanzees, a cross-sectional magnetic resonance imaging (MRI) study of the ages from 6 to 54 years (corresponds to the end of the juvenile stage to old age) indicated a gradual increase in the CC areas during this age-range, which was similar to that seen in humans. The only exception was found in the rostrum subdivision of the CC, with no significant increase during this age range \[[@pone.0179624.ref043]\]. Since the study did not include chimpanzees that were less than six years of age \[[@pone.0179624.ref043]\], whether there is a rapid increase in CC areas during infancy in chimpanzees, such as that seen in humans, is still unknown. How the rostrum develops during infancy is of particular interest, since the developmental trajectory after the juvenile stage in chimpanzees is different from that seen in humans. To investigate the developmental changes during infancy and the juvenile stage of the chimpanzee CC, we longitudinally quantified areas of the midsagittal total CC and the CC subdivisions of four chimpanzees from 1.8 months to six years of age (infancy to the juvenile stage), using MRI, and compared the results with those of humans. Materials and methods {#sec002} ===================== Participants {#sec003} ------------ ### Chimpanzees {#sec004} Four chimpanzees (one male and three females), whose ages ranged from 1.8 to 72 months, were longitudinally evaluated during development from infancy to the juvenile stage ([S1 Table](#pone.0179624.s003){ref-type="supplementary-material"}). In addition, ten adult chimpanzees were cross-sectionally evaluated as references ([S1 Table](#pone.0179624.s003){ref-type="supplementary-material"}). Adult chimpanzee characteristics were as follows: mean (s.d.) age, 31.2 (5.8) years; female/male ratio 30 percent male. All subjects lived within a social group of 14 individuals in an enriched environment with a 700-m^2^ outdoor compound enhanced by 15-m-high climbing frames and about 500 planted trees of approximately 60 species \[[@pone.0179624.ref044]\], as well as an attached indoor residence at the Primate Research Institute, Kyoto University (KUPRI) \[[@pone.0179624.ref045], [@pone.0179624.ref046]\]. Access to the outdoor compound was available to all chimpanzees every other day during the day. Daily meals included a wide variety of fresh fruits and vegetables fed throughout the day, supplemented with nutritionally balanced biscuits (fed twice daily) and water available *ad libitum*. The treatment of the chimpanzees was in accordance with the 2002 and 2010 version of the Guidelines for the Care and Use of Laboratory Primates issued by KUPRI. All care and experimental protocols were approved by the Animal Welfare and Animal Care Committee of the KUPRI. Of note, one of the longitudinally-followed chimpanzees had spinal cord compression due to osteogenesis imperfecta at the T8-T11 level of the thoracic vertebrae and had paraplegia and chronic renal dysfunction. She died from pneumonia at the age of two years. The disabled infant chimpanzee was raised by her biological mother in the social group. The caretakers and veterinarians closely monitored the mother and the infant, and provided the necessary care and treatments to minimize the suffering of the chimpanzee, in accordance with the Guidelines for the Care and Use of Laboratory Primates of the KUPRI. There were neither any symptoms suggesting brain abnormality nor noticeable MRI abnormalities of the brain. ### Humans {#sec005} We used part of the previously published numerical dataset from a human cross-sectional MRI study about midsagittal CC areas. Seventy-two healthy children (40 males, 32 females), whose ages ranged from one month to 126 months (see details in \[[@pone.0179624.ref038]\]), were analyzed ([S1 Table](#pone.0179624.s003){ref-type="supplementary-material"}). The comparison with human adult CC areas was based on the data from 14 healthy adults who served as controls \[[@pone.0179624.ref038]\]. Adult participant characteristics were as follows: mean (s.d.) age, 19.9 (1.9) years; female/male ratio, 50 percent male ([S1 Table](#pone.0179624.s003){ref-type="supplementary-material"}). All parents and adult participants gave written, informed consent for participation after the nature and possible consequences of the study were explained. All the protocols of the study were approved by the Committee on Medical Ethics of Toyama University (\#165). Image acquisition {#sec006} ----------------- ### Chimpanzees {#sec007} Three-dimensional, T1-weighted, whole-brain images were acquired with a 0.2 Tesla MR imager (Signa Profile; General Electric). The image data from three longitudinally evaluated chimpanzees (Ayumu, Cleo, and Pal) were acquired at the following time points: 6, 12, 24, 36, 48, 60, and 72 months. Another longitudinally evaluated chimpanzee (Pico) was scanned at the following time points: 1.8, 3, 4, 6, 9, and 24 months. The chimpanzees were anesthetized with ketamine (3.5 mg/kg) and medetomidine (0.035 mg/kg), and remained anesthetized with additional ketamine (1.75 mg/kg) and/or inhalation of isoflurane or sevoflurane as needed during the scans (total time anesthetized, approximately two hours). After the scans, they were reversed with atipamezole (0.175 mg/kg) and temporarily housed in a single home cage for recovery. During the scans, the chimpanzees were placed in the scanner chamber in a supine position with their heads fitted inside either the extremity coil (for the longitudinally evaluated chimpanzees) or the head coil (for the adult chimpanzees). For the four longitudinally-evaluated chimpanzees and four of the adult chimpanzees, a three-dimensional spoiled gradient-recalled acquisition in steady state (SPGR) sequence was obtained with the following acquisition parameters: repetition time (TR), 46 ms; echo time (TE), 10 ms; flip angle, 60°; slice thickness. 1.0--2.0 mm; field of view, 20--24 cm; matrix size, 256 × 256; number of excitations, two. For the other adult chimpanzees, a three-dimensional fast gradient echo with inversion recovery prep (FGRE-IrP) sequence was obtained with the following acquisition parameters: repetition time (TR), 32.3 ms; echo time (TE), 8.5 ms; flip angle, 40°; slice thickness, 1.5 mm; field of view, 24 cm; matrix size, 256 × 256; number of excitations, two. ### Humans {#sec008} The acquisition sequence and scan procedures of the human scan have been detailed in a previous publication \[[@pone.0179624.ref038]\]. Briefly, three-dimensional, T1-weighted, whole human-brain images were acquired with a 1.5 Tesla MR imager (Magnetom Vision; Siemens) using the fast low angle shot three-dimensional gradient refocused (GRE) sequence. The acquisition parameters were: repetition time (TR), 35 ms; echo time (TE), 6 ms; flip angle, 35°; slice thickness, 1.5 mm; field of view, 25.6 cm; matrix size, 256 × 256; number of excitations, one. Image processing {#sec009} ---------------- ### Total CC and CC subdivisions {#sec010} The midsagittal CC areas of the MRI for each individual were analyzed using Analyze 9.0 software (Mayo Clinic, Mayo Foundation, Rochester, MN, USA) in the following series of semi-manual procedures. (i) All images were converted into cubic voxel dimensions of 0.55 mm using a cubic spline interpolation algorithm. (ii) Brain image volumes were realigned to a standard anatomical orientation, with the transaxial plane parallel to the anterior commissure-posterior commissure line and perpendicular to the interhemispheric fissure. (iii) The midsagittal CC area measurements were obtained from the midsagittal slice in accordance with a method described by Witelson's studies \[[@pone.0179624.ref047], [@pone.0179624.ref048]\] and previous neuroimaging studies \[[@pone.0179624.ref022], [@pone.0179624.ref038], [@pone.0179624.ref043]\]. (iv) This method divides the total midsagittal CC area into the subdivisions of rostrum, genu, rostral body, anterior midbody, posterior midbody, isthmus, and splenium ([Fig 1](#pone.0179624.g001){ref-type="fig"}). To subdivide the total midsagittal CC area, the entire length of the total midsagittal CC area was first measured, and then divided into thirds. The anterior third was further divided into three regions by tracing a vertical line through the point where the anterior CC area began to curve back slightly. This resulted in three subdivisions: the rostrum; the genu; and the rostrum body. The middle third of the overall CC area was subdivided into equal sections, resulting in the anterior midbody and posterior midbody. Finally, the posterior third of the overall CC area was subdivided into the isthmus and splenium. The splenium was defined as the posterior fifth of the entire CC area; the remaining area within the posterior third was defined as the isthmus. Using the tracing tool, the area of the CC lying within each outlined region was measured in each individual. ![Regional subdivisions of the chimpanzee corpus callosum from a midsagittal view.\ The total CC midsagittal area was divided into seven equally spaced subdivisions: 1 = rostrum (red); 2 = genu (green); 3 = rostral body (yellow); 4 = anterior midbody (blue); 5 = posterior midbody (magenta); 6 = isthmus (cyan); 7 = splenium (white).](pone.0179624.g001){#pone.0179624.g001} Two evaluators (T.S. and K.O.), who were blinded to the sex and age of the subjects, semi-manually traced and measured the midsagittal CC areas. The intra-rater and inter-rater reproducibility of the CC measurements used in this study were evaluated. Ten brain scans were randomly selected for analysis. An analysis of intra-rater reproducibility was conducted using two sets of the brain measurements obtained by T.S. The inter-rater reproducibility was analyzed by comparing brain measurements obtained by T.S. and K.O. The Pearson's correlation coefficients for the comparisons of the results were r = 0.98 (intra-rater) and r = 0.97 (inter-rater), which indicated good reliability of the manual quantification. ### Normalization of the total CC and the CC subdivisions relative to adult areas {#sec011} To account for differences in the CC areas between adult chimpanzees and adult humans, the total CC and the CC subdivisions were normalized based on the average CC area of adult brains, and demonstrated as a percentage of adult areas (normalized area, hereafter). Since the ages of the adult chimpanzees tended to be older than that of adult humans, we investigated the effects of age on areas of total CC and the CC subdivisions in these two adult groups using a linear regression model. Total CC and the CC subdivisions served as the dependent variables. Age was introduced as an independent variable. There were no significant age-dependent changes in total CC or the CC subdivisions in either species ([S2 Table](#pone.0179624.s004){ref-type="supplementary-material"}). Therefore, we concluded that the adult chimpanzees and adult humans were comparable to serve as the adult control groups, given that their callosal measures were stable with respect to age. Definitions of developmental stages {#sec012} ----------------------------------- In chimpanzees, the developmental stages were defined as follows: "infancy" corresponded to \~12 months of age, and the "juvenile stage" corresponded to \~84 months of age; in humans, these designations corresponded to \~24 months of age and \~144 months of age, respectively. The developmental stages were applied based on previous publications that used the first eruption of the first deciduous tooth \[[@pone.0179624.ref031], [@pone.0179624.ref032]\], weight increase \[[@pone.0179624.ref029], [@pone.0179624.ref034]\], and sexual maturation (menarche, first ejaculation) \[[@pone.0179624.ref030], [@pone.0179624.ref033], [@pone.0179624.ref035], [@pone.0179624.ref036]\]. The longitudinally evaluated chimpanzees of this study were observed to undergo sexual maturation at the age of seven years. Statistical analysis {#sec013} -------------------- We investigated subdivision-specific developmental trajectories in each species. For the chimpanzee study, the MRIs were obtained longitudinally from four young chimpanzees from 1.8 to 72 months of age. For the human study, MRIs were obtained from 72 children between the ages of one month and 126 months, using a cross-sectional design. These differences in study design and number of participants made the cross-species statistical comparison difficult. Therefore, we decided to remain descriptive in highlighting the similarities and differences between chimpanzees and humans, as previously reported \[[@pone.0179624.ref049]--[@pone.0179624.ref051]\]. ### Developmental trajectories of the total CC and the subdivisions {#sec014} The relationships between the age and the CC areas were investigated by polynomial regression analyses. *F*-tests were used to determine whether the order of a developmental model was cubic, quadratic, or linear. First, linear, quadratic, or cubic polynomial regression models were fitted by age using R.v. 3.2.2 software to identify the developmental patterns in the total CC and the CC subdivisions. If a cubic model did not yield significant results, a quadratic model was tested; if a quadratic model did not yield significant results, a linear model was tested. Thus, a growth model was polynomial/nonlinear if either the cubic or quadratic term significantly contributed to the regression equation. The Akaike information (a log-likelihood function) \[[@pone.0179624.ref052]\] was used to ensure effective model selection. Second, using R.v. 3.2.2 software, the data that showed nonlinear trajectories were fitted by locally weighted polynomial regression (LOESS) \[[@pone.0179624.ref053]\]. In this way, even with relatively few data points, the age-related area size changes could be delineated by applying the curve-fitting suggested by previous human studies \[[@pone.0179624.ref054], [@pone.0179624.ref055]\] and chimpanzee studies \[[@pone.0179624.ref049]--[@pone.0179624.ref051]\], without enforcing a common parametric function on the dataset, as is the case with linear polynomial models. For the fit at age X, the fit is made using values in the neighborhood of X, each weighted by the distance from X. The size of the neighborhood is defined by alpha. Data were fitted in four interactions with alpha = 0.70, in accordance with previous MRI studies \[[@pone.0179624.ref049]--[@pone.0179624.ref051], [@pone.0179624.ref055]\]. The observed and fitted values of the total CC and the CC subdivisions were plotted as a function of age to display the age-related change. The analysis was performed on the original CC areas as well as on the normalized CC areas (% of adult area, as described in the Section "Normalization of the total CC and the CC subdivisions relative to adult areas"). ### Difference in normalized areas among CC subdivisions {#sec015} We investigated the differences between the normalized areas among the CC subdivisions. This was motivated by a previous chimpanzee MRI study that indicated that there was no increase in the rostrum area in chimpanzees after the juvenile stage, while other subdivisions still developed \[[@pone.0179624.ref043]\]. This suggested that each subdivision has specific developmental features, and the features are potentially species-specific. Since the study design (longitudinal vs. cross-sectional) and the number of participants (four chimpanzees vs. 72 humans) were different between the two species, we applied different statistical methods for each species. For the longitudinal dataset of the young chimpanzees, the nonparametric one-way analysis of variance (ANOVA) with repeated measures (Friedman test) (*η* ^*2*^ and *p* values) was applied to investigate within-group differences among the seven CC subdivisions. The CC subdivisions served as the test variables. When the Friedman test yielded a significant effect (p \< 0.05), a post hoc analysis was performed using a Dunn\'s test for nonparametric pairwise comparisons between assessments, with a Bonferroni correction applied, resulting in a significance level set at *p* \< 0.05. For the cross-sectional dataset of the young humans, the parametric one-way ANOVA with repeated measures (*F* and *p* values) was applied to investigate within-group differences among the seven CC subdivisions. The CC subdivisions served as the within-subjects variables. Age was a covariate. When the parametric one-way ANOVA with repeated measures yielded a significant effect (*p* \< 0.05), a post hoc analysis was performed using a paired t-test for parametric pairwise comparisons between assessments, with a Bonferroni correction applied, resulting in a significance level set at *p* \< 0.05. Results {#sec016} ======= Evaluation of the developmental trajectory of the total CC and the subdivisions {#sec017} ------------------------------------------------------------------------------- ### Chimpanzees {#sec018} Overall, the results of the total CC and the CC subdivisions revealed noteworthy developmental changes in chimpanzees throughout the study period (1.8 to 72 months) ([Fig 2](#pone.0179624.g002){ref-type="fig"}, Tables [1](#pone.0179624.t001){ref-type="table"}, [2](#pone.0179624.t002){ref-type="table"} and [3](#pone.0179624.t003){ref-type="table"}, and [S1 Table](#pone.0179624.s003){ref-type="supplementary-material"}). The total CC followed a nonlinear developmental trajectory (*F* = 50.99, cubic effect, *p* = 2.55×10^−10^) ([Table 3](#pone.0179624.t003){ref-type="table"}). All of the CC subdivisions also increased nonlinearly (rostrum, *F* = 23.39, cubic effect, *p* = 3.58×10^−7^; genu, *F* = 57.56, cubic effect, *p* = 7.56×10^−11^; rostral body, *F* = 11.73, cubic effect, *p* = 7.31×10^−5^; anterior midbody, *F* = 25.51, cubic effect, *p* = 1.69×10^−7^; posterior midbody, *F* = 22.02, cubic effect, *p* = 5.98×10^−7^; isthmus, *F* = 25.29, cubic effect, *p* = 1.83×10^−7^; splenium, *F* = 27.31, quadratic effect, *p* = 3.17×10^−6^) ([Table 3](#pone.0179624.t003){ref-type="table"}). LOESS scatter plots for the area of the total CC and the subdivisions (in mm^2^) are demonstrated in [Fig 3](#pone.0179624.g003){ref-type="fig"}, and the normalized total CC and the subdivisions (in %) are demonstrated in [Fig 4](#pone.0179624.g004){ref-type="fig"}. ![An ontogenetic series of the regional subdivisions of the chimpanzee corpus callosum from a midsagittal view.\ Regional subdivisions: 1 = rostrum (red); 2 = genu (green); 3 = rostral body (yellow); 4 = anterior midbody (blue); 5 = posterior midbody (magenta); 6 = isthmus (cyan); 7 = splenium (white). The bars below the figures indicate the developmental stage. The indicated developmental stages are infancy (open bar), the juvenile stage (hatched bar), and the adult stage (horizonal striped bar).](pone.0179624.g002){#pone.0179624.g002} ![Evaluation of the corpus callosum areas during development.\ Age-related changes in the total CC and the CC subdivisions during infancy and the juvenile stage are shown for chimpanzees (n = 4) and humans (n = 72). (A) total, (B) rostrum, (C) genu, (D) rostral body, (E) anterior midbody, (F) posterior midbody, (G) isthmus, and (H) splenium. The bar below the graphs indicates the developmental stage. The indicated developmental stages are infancy (open bar) and the juvenile stage (hatched bar).](pone.0179624.g003){#pone.0179624.g003} ![Evaluation of the normalized corpus callosum areas during development.\ Age-related changes in the total CC and the CC subdivisions relative to the adult areas during infancy and the juvenile stage are shown for chimpanzees (n = 4) and humans (n = 72). (A) total, (B) rostrum, (C) genu, (D) rostral body, (E) anterior midbody, (F) posterior midbody, (G) isthmus, and (H) splenium. The bar below the graphs indicates the developmental stage. The indicated developmental stages are infancy (open bar) and the juvenile stage (hatched bar).](pone.0179624.g004){#pone.0179624.g004} 10.1371/journal.pone.0179624.t001 ###### Sample characteristics of the corpus callosum areas in chimpanzees. ![](pone.0179624.t001){#pone.0179624.t001g} ---------------------------------------------------------- -------- ------- Infants (age≤12 mons) (Number of scans = 11) Region Median IQR Total CC 134.60 55.02 Rostrum 4.79 2.99 Genu 22.43 13.75 Rostral body 23.93 8.37 Anterior midbody 18.54 5.69 Posterior midbody 14.95 3.89 Isthmus 11.07 3.89 Splenium 33.20 17.64 Juveniles (12 mons \<age≤84 mons) (Number of scans = 16) Region Median IQR Total CC 204.72 45.23 Rostrum 7.18 2.31 Genu 48.30 2.99 Rostral body 32.45 10.54 Anterior midbody 23.33 4.49 Posterior midbody 21.39 6.06 Isthmus 16.45 5.01 Splenium 50.55 18.99 ---------------------------------------------------------- -------- ------- Month, mon; interquartile range, IQR. Area size characteristics of the sample classified into subgroups according to developmental stage. In chimpanzee scans (Longitudinal scan, n = 4), values represent median and IQR measured area (mm^2^). 10.1371/journal.pone.0179624.t002 ###### Sample characteristics of the corpus callosum areas relative to adult areas (normalized areas) in chimpanzees. ![](pone.0179624.t002){#pone.0179624.t002g} ---------------------------------------------------------- -------- ------- Infants (age≤12 mons) (Number of scans = 11) Region Median IQR Total CC 40.70 16.64 Rostrum 46.97 29.32 Genu 31.70 19.43 Rostral body 43.35 15.16 Anterior midbody 42.55 13.06 Posterior midbody 37.62 9.78 Isthmus 39.13 13.74 Splenium 40.02 21.27 Juveniles (12 mons \<age≤84 mons) (Number of scans = 16) Areas Median IQR Total CC 61.90 13.67 Rostrum 70.41 22.70 Genu 68.26 4.23 Rostral body 58.78 19.08 Anterior midbody 53.54 10.30 Posterior midbody 58.14 17.69 Isthmus 60.93 22.90 Splenium 61.90 13.67 ---------------------------------------------------------- -------- ------- Month, mon; interquartile range, IQR. Area size characteristics of the sample classified into subgroups according to developmental stage. In chimpanzee scans (Longitudinal scan, n = 4), values represent median and IQR normalized area of the adult area (%). 10.1371/journal.pone.0179624.t003 ###### Results of polynomial regression modeling of the developmental trajectories of the corpus callosum areas. ![](pone.0179624.t003){#pone.0179624.t003g} Species Region Best fitting model *F* *R*^*2*^ sig ------------------- ----------- -------------------- ------- ---------------- ---------------- Chimpanzees Total CC Cubic 50.99 0.85 2.55×10^−10^ Rostrum Cubic 23.39 0.72 3.58×10^−7^ Genu Cubic 57.56 0.87 7.56×10^−11^ Rostral body Cubic 11.73 0.55 7.31×10^−5^ Anterior midbody Cubic 25.51 0.74 1.69×10^−7^ Posterior midbody Cubic 22.02 0.71 5.98×10^−7^ Isthmus Cubic 25.29 0.74 1.83×10^−7^ Splenium Quadratic 27.31 0.67 3.17×10^−6^ Humans Total Cubic 86.42 0.78 \<2.20×10^−16^ Rostrum Cubic 7.50 0.22 2.08×10^−4^ Genu Cubic 73.64 0.75 \<2.20×10^−16^ Rostral body Cubic 25.94 0.51 2.67×10^−11^ Anterior midbody Cubic 69.56 0.74 \<2.20×10^−16^ Posterior midbody Cubic 59.62 0.71 \<2.20×10^−16^ Isthmus Cubic 36.71 0.60 3.18×10^−14^ Splenium Cubic 52.42 0.68 \<2.20×10^−16^ Age-related changes in the total CC and the CC subdivisions in chimpanzees (n = 4) and in humans (n = 72). *F* = *F* value, *R*^*2*^ = adjusted *R*^*2*^ value. "Best fitting model," "*F*," "*R*^*2*^," and "sig" indicate the results of the statistical analysis of the age-related changes in the total CC and the CC subdivisions with a polynomial regression model. The best-fitting model represents the best-fitting model of the linear, quadratic, and cubic regression models. ### Humans {#sec019} As observed in chimpanzees, the results of the total CC and the CC subdivisions revealed noteworthy developmental changes in humans through the study period (one month to 126 months) ([Fig 2](#pone.0179624.g002){ref-type="fig"}, Tables [3](#pone.0179624.t003){ref-type="table"}, [4](#pone.0179624.t004){ref-type="table"} and [5](#pone.0179624.t005){ref-type="table"}, and [S1 Table](#pone.0179624.s003){ref-type="supplementary-material"}). The total CC followed a nonlinear developmental trajectory (*F* = 86.42, cubic effect, *p* \< 2.20×10^−16^) ([Table 5](#pone.0179624.t005){ref-type="table"}). All of the CC subdivisions also increased nonlinearly (rostrum, *F* = 7.50, cubic effect, *p* = 2.08×10^−4^; genu, *F* = 73.64, cubic effect, *p* \< 2.20×10^−16^; rostral body, *F* = 25.94, cubic effect, *p* \< 2.67×10^−11^; anterior midbody, *F* = 69.56, cubic effect, *p* \< 2.20×10^−16^; posterior midbody, *F* = 59.62, cubic effect, *p* \< 2.20×10^−16^; isthmus, *F* = 36.71, cubic effect, *p* = 3.18×10^−14^; and splenium, *F* = 52.42, quadratic effect, *p* \< 2.20×10^−16^) ([Table 5](#pone.0179624.t005){ref-type="table"}). LOESS scatter plots for the area of the total CC and the subdivisions (in mm^2^) are demonstrated in [Fig 3](#pone.0179624.g003){ref-type="fig"}, and the normalized total CC and the subdivisions (in %) are demonstrated in [Fig 4](#pone.0179624.g004){ref-type="fig"}. 10.1371/journal.pone.0179624.t004 ###### Sample characteristics of the corpus callosum areas in humans. ![](pone.0179624.t004){#pone.0179624.t004g} ----------------------------------------------------------- -------- -------- Infants (age≤24 mons) (Number of scans = 36) Region Mean SD Total CC 309.64 109.87 Rostrum 10.084 5.32 Genu 67.53 32.06 Rostral body 53.83 16.91 Anterior midbody 34.28 13.24 Posterior midbody 30.64 10.56 Isthmus 21.75 7.87 Splenium 91.53 33.98 Juveniles (24 mons \<age≤144 mons) (Number of scans = 36) Region Mean SD Total CC 481.11 92.75 Rostrum 14.75 5.08 Genu 111.7 16.95 Rostral body 71.14 13.38 Anterior midbody 53.06 10.50 Posterior midbody 48.92 8.75 Isthmus 38.17 8.08 Splenium 143.42 28.50 ----------------------------------------------------------- -------- -------- Month, mon; standard deviation, SD. Area size characteristics of the sample classified into subgroups according to developmental stage. In human scans (Cross-sectional scan, n = 72), values represent mean and SD normalized area of the adult area (%). 10.1371/journal.pone.0179624.t005 ###### Sample characteristics of the corpus callosum areas relative to adult areas (normalized areas) in humans. ![](pone.0179624.t005){#pone.0179624.t005g} ----------------------------------------------------------- ------- ------- Infants (age≤24 mons) (Number of scans = 36) Region Mean SD Total CC 51.83 18.39 Rostrum 47.05 24.80 Genu 49.45 23.49 Rostral body 62.70 19.69 Anterior midbody 51.60 30.48 Posterior midbody 49.88 17.19 Isthmus 44.32 16.03 Splenium 51.82 19.24 Juveniles (24 mons \<age≤144 mons) (Number of scans = 36) Region Mean SD Total CC 80.53 8.94 Rostrum 68.83 23.70 Genu 81.76 12.41 Rostral body 82.86 15.59 Anterior midbody 79.87 10.62 Posterior midbody 79.63 11.30 Isthmus 77.78 16.46 Splenium 81.19 11.35 ----------------------------------------------------------- ------- ------- Month, mon; standard deviation, SD. Area size characteristics of the sample classified into subgroups according to developmental stage. In human scans (Cross-sectional scan, n = 72), values represent mean and SD measured area (mm^2^). Evaluation of regional variation in normalized areas among CC subdivisions {#sec020} -------------------------------------------------------------------------- ### Chimpanzees {#sec021} The nonparametric Friedman test indicated a significant main effect of the normalized subdivision areas (*η* ^*2*^ = 25.94, *P* = 2.29×10^−4^). Post hoc tests using a Dunn\'s test showed that the area of the rostrum differed significantly from that of the anterior midbody (*P* = 0.003), the posterior midbody (*P* = 0.002), and the isthmus (*P* = 0.007) ([Table 6](#pone.0179624.t006){ref-type="table"}). The LOESS curves of the normalized CC subdivisions indicated that the increase was most rapid in the rostrum, compared to the other CC subdivisions, and the area reached close to 100% of the adult area by the end of the juvenile stage ([Fig 4B--4H](#pone.0179624.g004){ref-type="fig"}). 10.1371/journal.pone.0179624.t006 ###### Differences in normalized areas among CC subdivisions in chimpanzees. ![](pone.0179624.t006){#pone.0179624.t006g} ------------------- ----------------- ------- -------------- ------------------ ------------------- --------- ---------- Rostrum Genu Rostral body Anterior midbody Posterior midbody Isthmus Splenium Rostrum Genu 1.000 Rostral body 1.000 1.000 Anterior midbody [**.003**]{.ul} 1.000 .294 Posterior midbody [**.002**]{.ul} 1.000 .247 1.000 Isthmus [**.007**]{.ul} 1.000 .557 1.000 1.000 Splenium .064 1.000 1.000 1.000 1.000 1.000 ------------------- ----------------- ------- -------------- ------------------ ------------------- --------- ---------- Values present Bonferroni-corrected *P* values. Underlined bold characters indicate a significant difference between CC subdivisions. ### Humans {#sec022} The parametric one-way repeated measures ANOVA indicated a significant main effect of subdivisions (*F* = 6.98, *P* = 4.4E-07). There was a significant interaction for age-by-subdivisions (*F* = 3.77, *P* = 0.001). Post hoc tests using a paired t-test showed that the area of the rostral body differed significantly from that of the rostrum (*P* = 7.0E-07), the genu (*P* = 0.004), the anterior midbody (*P* = 2.0E-04), the posterior midbody (*P* = 4.1E-04), the isthmus (*P* = 2.6E-06), and the splenium (*P* = 1.4E-03) ([Table 7](#pone.0179624.t007){ref-type="table"}). The LOESS curves of the normalized CC subdivisions indicated that the area of the rostral body was greater than that of the other CC subdivisions at the onset of infancy, and the area reached more than 80% of the adult area by the end of infancy ([Fig 4B--4H](#pone.0179624.g004){ref-type="fig"}). 10.1371/journal.pone.0179624.t007 ###### Differences in normalized areas among CC subdivisions in humans. ![](pone.0179624.t007){#pone.0179624.t007g} ------------------- -------------------- ----------------- -------------------- ------------------ ------------------- --------- ---------- Rostrum Genu Rostral body Anterior midbody Posterior midbody Isthmus Splenium Rostrum Genu .286 Rostral body [**7.0E-07**]{.ul} [**.004**]{.ul} Anterior midbody .164 1.000 [**2.0E-04**]{.ul} Posterior midbody .500 1.000 [**4.1E-04**]{.ul} 1.000 Isthmus 1.000 .582 [**2.6E-06**]{.ul} .168 .560 Splenium .077 1.000 [**1.4E-03**]{.ul} 1.000 1.000 .050 ------------------- -------------------- ----------------- -------------------- ------------------ ------------------- --------- ---------- Values present Bonferroni-corrected *P* values. Underlined bold characters indicate a significant difference between CC subdivisions. Descriptive comparison of developmental trajectories of the total CC between chimpanzees and humans {#sec023} --------------------------------------------------------------------------------------------------- ### Similarities between chimpanzees and humans {#sec024} There were two noticeable similarities. First, the total CC increased rapidly during infancy and continued to increase slowly during the juvenile stage in both species ([Fig 4A](#pone.0179624.g004){ref-type="fig"}). Second, the normalized total CC at the beginning of infancy was similarly small in both species. It was 25% in chimpanzees and 31% in humans ([Fig 4A](#pone.0179624.g004){ref-type="fig"}). ### Differences between chimpanzees and humans {#sec025} There were two noticeable differences between chimpanzees and humans. First, although the total CC increased rapidly during infancy in both species, the slope was steeper in humans than in chimpanzees. The total CC of the chimpanzees increased 220% during infancy, while the increase was 238% in humans ([Fig 3A](#pone.0179624.g003){ref-type="fig"}). Second, at the end of the juvenile stage, the normalized total CC of humans was greater than that of chimpanzees. In humans, the normalized area reached 85% at the end of the juvenile stage, while it remained at 71% in chimpanzees ([Fig 4A](#pone.0179624.g004){ref-type="fig"}). Descriptive comparison of developmental trajectories of the CC subdivisions between chimpanzees and humans {#sec026} ---------------------------------------------------------------------------------------------------------- ### Similarities between chimpanzees and humans {#sec027} There were three noticeable similarities between chimpanzees and humans. First, the proportion of each CC subdivision was similar between the two species. In adult chimpanzees, the areas of the rostrum, genu, rostral body, anterior midbody, posterior midbody, isthmus, and the splenium were 3, 21, 17, 13, 12, 9, and 25% of the total CC, respectively ([S1 Table](#pone.0179624.s003){ref-type="supplementary-material"}). The corresponding values for humans were 4, 23, 14, 11, 10, 8, and 30% of the total, respectively ([S1 Table](#pone.0179624.s003){ref-type="supplementary-material"}). Second, the relative area of the CC subdivisions at the beginning of infancy was similar in both species, except for the rostral body (detailed in the Section "Differences between chimpanzees and humans"). In chimpanzees, the normalized CC subdivision areas at the beginning of infancy were 31% in the rostrum, 19% in the genu, 29% in the anterior midbody, 27% in the posterior midbody, 27% in the isthmus, and 25% in the splenium ([Fig 4B, 4C and 4E--4H](#pone.0179624.g004){ref-type="fig"}). The values in humans were 31% in the rostrum, 22% in the genu, 30% in the anterior midbody, 33% in the posterior midbody, 30% in the isthmus, and 33% in the splenium ([Fig 4B, 4C and 4E--4H](#pone.0179624.g004){ref-type="fig"}). Finally, areas of the CC subdivisions increased rapidly during infancy and continued to increase slowly during the juvenile stage in both species ([Fig 4C--4H](#pone.0179624.g004){ref-type="fig"}). The only exception was the rostrum of chimpanzees, which is detailed in in the Section "Differences between chimpanzees and humans". ### Differences between chimpanzees and humans {#sec028} There were four noticeable differences between the two species. First, at the beginning of infancy, the normalized rostral body area of humans was greater than that of other CC subdivisions, and, by the end of infancy, it had already reached 83% of that of the adult. This prominence of the rostral body was not seen in chimpanzees. In humans, the normalized rostral body area expands from 43% to 83% during infancy, while this expansion ranged from 26% to 60% in chimpanzees ([Fig 4D](#pone.0179624.g004){ref-type="fig"}). Second, although areas of the CC subdivisions increased rapidly during infancy in both species, the slope was steeper in humans than in chimpanzees. In chimpanzees, the normalized areas of the CC subdivisions expanded during infancy from 19 to 61% in the genu, from 26 to 60% in the rostral body, from 29 to 51% in the anterior midbody, from 27 to 48% in the posterior midbody, from 27 to 50% in the isthmus, and from 25 to 51% in the splenium ([Fig 4C--4H](#pone.0179624.g004){ref-type="fig"}). In humans, the corresponding values were: from 22% to 80% in the genu; from 43% to 83% in the rostral body; from 30% to 74% in the anterior midbody; from 33% to 69% in the posterior midbody; from 30% to 65% in the isthmus; and from 33% to 72% in the splenium ([Fig 4C--4H](#pone.0179624.g004){ref-type="fig"}). Third, the normalized areas and the CC subdivisions of humans were greater than that of chimpanzees, except for the rostrum, at the end of the juvenile stage. In chimpanzees, the normalized areas were: 75% in the genu; 73% in the rostral body; 64% in the anterior midbody; 67% in the posterior midbody; 68% in the isthmus; and 72% in the splenium at the end of juvenile stage ([Fig 4C--4H](#pone.0179624.g004){ref-type="fig"}). In humans, the corresponding values were: 85% in the genu; 89% in the rostral body; 84% in the anterior midbody; 81% in the posterior midbody; 82% in the isthmus; and 88% in the splenium ([Fig 4C--4H](#pone.0179624.g004){ref-type="fig"}). Finally, the area of the rostrum of the chimpanzees increased more rapidly during the juvenile stage than that of the humans, and the area at the end of the juvenile stage was close to that of adults. In chimpanzees, the normalized area of the rostrum increased from 64% to 94% during juvenile stage ([Fig 4B](#pone.0179624.g004){ref-type="fig"}), while, in humans, the increase was from 66% to 72% ([Fig 4B](#pone.0179624.g004){ref-type="fig"}). Discussion {#sec029} ========== General inter-species similarities and differences in the developmental trajectories {#sec030} ------------------------------------------------------------------------------------ The major finding in this study was the identification, in chimpanzees, of a rapid increase in the total CC and the subdivisions during infancy, followed by a gradual increase during the juvenile stage. This developmental trajectory was similar to that reported in humans, and the increase was attributed to the formation of myelin sheaths around the axons that pass through the CC \[[@pone.0179624.ref019], [@pone.0179624.ref020], [@pone.0179624.ref024], [@pone.0179624.ref037], [@pone.0179624.ref038], [@pone.0179624.ref041], [@pone.0179624.ref056]\]. Accordingly, diffusion tensor imaging studies of human brains have shown that the fractional anisotropy---a measure that reflects axonal alignment, density, and myelination---increases during development \[[@pone.0179624.ref037], [@pone.0179624.ref041], [@pone.0179624.ref057]--[@pone.0179624.ref060]\], with a reduction in radial diffusion \[[@pone.0179624.ref061]\], indicating that myelination is the major cause of the volume increase. The major differences between humans and chimpanzees were the slope of the developmental curve during infancy, which was steeper in humans than in chimpanzees, and the normalized CC areas during the juvenile stage, both of which were greater in humans than in chimpanzees (inter-species differences in the rostral body and the rostrum are discussed in the Sections "Development of the rostral body" and "Development of the rostrum"). These findings are congruent with a previous volumetric study, which indicated that cerebral volume and the substructures increased more rapidly in humans than in chimpanzees \[[@pone.0179624.ref050]\]. Since early infancy is critical for postnatal brain development in humans, in terms of volume increase \[[@pone.0179624.ref062], [@pone.0179624.ref063]\], synaptic elaboration, myelination \[[@pone.0179624.ref064]\], and the establishment of a default mode network \[[@pone.0179624.ref065]\], inter-species differences during this period might be related to the functional differences between humans and chimpanzees. Whether the emergence of the rapid increase during infancy is a marker of hominoids needs to be elucidated. Development of the rostral body {#sec031} ------------------------------- The development of the human rostral body was characterized by a greater normalized area than other CC subdivisions and a rapid increase during infancy than that of chimpanzees. This early maturation might indicate evolutional changes in brain anatomy and functions. The rostral body carries fibers between the medial prefrontal and premotor cortices \[[@pone.0179624.ref066]\]. These cortical regions play an important role in behavior planning and control, such as response preparation, selection, and response control \[[@pone.0179624.ref067]--[@pone.0179624.ref069]\]. A DTI study of pediatric human traumatic brain injury suggested that the degree of damage in the rostral body is related to verbal working memory and mathematical concepts. A reduction in the area was also related to attention deficit hyperactivity disorder \[[@pone.0179624.ref070]\]. Since the functions related to the rostral body, which can be summarized as "executive functions," are highly specialized in humans, one might argue that the early maturation seen in humans is related to cognitive and behavioral differences between humans and other hominoids. This concept must be further investigated. Development of the rostrum {#sec032} -------------------------- The development of the chimpanzee rostrum was characterized by a faster increase during the juvenile stage than that of humans. The size of the area at the end of the juvenile stage was close to that of an adult. This explained why the increase in the rostrum area was not observed in the previous study that targeted chimpanzees older than our study population \[[@pone.0179624.ref043]\]. A histological evaluation of the primate brain showed that the rostrum carries fibers between the orbitofrontal and dorsolateral prefrontal cortices \[[@pone.0179624.ref007]\]. These regions are important for different processes of attention: the orbitofrontal cortex controls emotional motivation behavior, and the dorsolateral prefrontal cortex monitors cognition to develop efficient control of interfering sensory stimuli \[[@pone.0179624.ref071]\]. Accordingly, the rostrum is involved in the development of attention and inhibitory control \[[@pone.0179624.ref072]--[@pone.0179624.ref074]\], and the transfer of information between prefrontal cortices \[[@pone.0179624.ref075]\]. In chimpanzees, inhibitory control of saccades was weaker than that of humans, which led to frequent saccades and short fixations of eye movement \[[@pone.0179624.ref076]--[@pone.0179624.ref078]\]. Taken together, the development of the rostrum in chimpanzees might be related to inter-species differences in attention and inhibitory control. The scientific environment in chimpanzee research and the use of legacy data {#sec033} ---------------------------------------------------------------------------- In the USA, the National Institutes of Health (NIH) has ceased all invasive biomedical studies on chimpanzees \[[@pone.0179624.ref079]--[@pone.0179624.ref081]\]. In 2013, the NIH had decided to retire more than 300 chimpanzees, leaving 50 chimpanzees for research in case of a public-health emergency. In 2015, the NIH made the decision that they would send this remaining population to sanctuaries in subsequent years. Thus, there was a push to repurpose legacy chimpanzee brain data. After the NIH decision in 2015, a biobank of chimpanzee brains, including MRI data, was developed through NIH funding for public use (<http://www.chimpanzeebrain.org/>). In Japan, our longitudinal MRI study of chimpanzee infants began in KUPRI in 2000 \[[@pone.0179624.ref049], [@pone.0179624.ref050]\], and terminated in 2012. Despite the relatively small sample size, which makes statistical analysis difficult, this longitudinally evaluated cohort is still precious and might contribute to the research community, since such a longitudinal dataset does not exist in the biobank in the USA, and it is difficult to collect new data for use now and in the future. Chimpanzees are among the endangered species and must be protected. Limitations {#sec034} ----------- There are several limitations to our study. First, one of the chimpanzees in the present study, Pico, died at the age of two years, and had complications from spinal cord compression with paraplegia. Although there was no noticeable abnormality on the brain MRI, the existence of a subtle abnormality was difficult to detect during routine radiological evaluation. Therefore, we also analyzed the developmental trajectories without Pico's data. We found that the results without Pico's data did not change our conclusion obtained from the full dataset ([S1](#pone.0179624.s001){ref-type="supplementary-material"} and [S2](#pone.0179624.s002){ref-type="supplementary-material"} Figs; [S3 Table](#pone.0179624.s005){ref-type="supplementary-material"}; [S1 File](#pone.0179624.s006){ref-type="supplementary-material"}). Second, in our study, the adult chimpanzees (used as references to normalize areas of the CC and the subdivisions) were scanned using two different protocols (SPGR or FGRE-IrP). To investigate the effect of scan protocol on image quantification, we compared the midsagittal CC area in a brain sample from an adult chimpanzee, scanned with SPGR and FGRE-IrP ([S2 File](#pone.0179624.s007){ref-type="supplementary-material"}). We found that the CC area, as measured by the two MRI sequences, are indeed close (0.2% difference) and comparable to the intra-rater difference for the manual delineation (1.7%). Therefore, we assumed that the difference in the scan protocol had little effect on the quantification of the CC area ([S2 File](#pone.0179624.s007){ref-type="supplementary-material"}). Since chimpanzee brain MRIs available for research purposes are limited, it is common to combine MRIs scanned with different scanners and acquisition sequences \[[@pone.0179624.ref043]\]. We recognize that the issue related to the heterogeneity of MRIs is one of the limitations generally seen in the field of chimpanzee neuroimaging studies. Third, the prenatal period was not included in the present study. The inclusion of prenatal development is important since neuronal maturation at birth varies across species \[[@pone.0179624.ref082]\]. One possibility to enable the evaluation of prenatal development is to utilize longitudinally-acquired, legacy sonography data \[[@pone.0179624.ref051]\], which might make for an interesting future study. Fourth, we defined developmental stages based on physical milestones, such as dental eruption, weight increase, and sexual maturation for the interspecies comparison, since this anthropological definition is a valid approach by which to compare the development among different primates \[[@pone.0179624.ref049], [@pone.0179624.ref050], [@pone.0179624.ref083]\]. However, the relationship between physical and neuronal development is not fully understood. The appropriateness of developmental staging based on neuronal milestones has yet to be investigated. Finally, the method used to draw the boundaries of the seven CC subdivisions on T1-weighted MRI was based on the studies about the topographical organization of the white matter fibers of the adult human brain. The applicability of the MRI-based anatomical definition throughout different developmental stages has not been fully validated. Cross-species longitudinal evaluation of the topological organization of CC fibers during development is essential for validation. In summary, our results suggest that CC development in chimpanzees and humans is characterized by a rapid increase during infancy, followed by a relatively slow increase during the juvenile stage. The differences between the two species include a tendency toward a greater increase in the human CC areas, especially in the rostral body, during infancy, compared to that observed in chimpanzees. A tendency toward a greater increase in the rostrum during the juvenile stage in chimpanzees, compared to that observed in humans, was also observed. The interspecies differences in the developmental trajectories of the rostral body and the rostrum might underpin evolutional changes in the executive functions related to these areas. Supporting information {#sec035} ====================== ###### Evaluation of the rostrum and genu during development in young chimpanzee data with and without Pico's data. Age-related changes in the rostrum and genu during infancy and the juvenile stage (6 to 72 months) are shown for chimpanzees with and without Pico's data (n = 4; n = 3). (A) rostrum, (B) genu. The bar below the graphs indicates the developmental stage. The indicated developmental stages are infancy (open bar) and the juvenile stage (hatched bar). (PDF) ###### Click here for additional data file. ###### Evaluation of the normalized rostrum and genu during development in chimpanzee data with and without Pico's data. Age-related changes in the rostrum and genu, relative to the adult areas, during infancy and the juvenile stage (6 to 72 months) are shown for chimpanzees with and without Pico's data (n = 4; n = 3). (A) rostrum, (B) genu. The bar below the graphs indicates the developmental stage. The indicated developmental stages are infancy (open bar) and the juvenile stage (hatched bar). (PDF) ###### Click here for additional data file. ###### Age, total CC, and CC subdivisions in chimpanzees and humans during the developmental course of the study period. (PDF) ###### Click here for additional data file. ###### Results of the linear regression model of age-related changes in the corpus callosum areas during the adult stage. Age-related changes in the total CC and the CC subdivisions during the adult stage (n = 10; mean (s.d.) age, 31.2 (5.8) years). *F* = *F* value, *R*^*2*^ = adjusted *R*^*2*^ value. "*F*," "*R*^*2*^," and "sig" indicate the results of the statistical analysis for the age-related changes in the total CC and the CC subdivisions with a linear regression model. "n.s." indicates "not significant." (DOCX) ###### Click here for additional data file. ###### Results of polynomial regression modeling of the developmental trajectories of the rostrum and genu in chimpanzees with and without Pico's data. Age-related changes in the rostrum and genu in chimpanzees with and without Pico's data (n = 4; n = 3). *F* = *F* value, *R*^*2*^ = adjusted *R*^*2*^ value. "Best fitting model," "*F*" "*R*^*2*^," and "sig" indicate the results of the statistical analysis for the age-related changes in the rostrum and genu with a polynomial regression model. The best-fitting model represents the best-fitting model of the linear, quadratic, and cubic regression models. (DOCX) ###### Click here for additional data file. ###### Comparison of the developmental trajectories of the rostrum and genu in young chimpanzees with and without Pico's data. (DOCX) ###### Click here for additional data file. ###### Comparison of the measurements of the chimpanzee CC area acquired with different MRI sequences. (DOCX) ###### Click here for additional data file. We thank T. Nishimura, A. Watanabe, A. Kaneko, S. Goto, S. Watanabe, K. Kumazaki, N. Maeda, M. Tanaka, M. Hayashi, T. Imura, and K. Matsubayashi for assisting with the care of chimpanzees during scanning. We also thank the personnel at the Centre for Human Evolution Modelling Research at KUPRI for daily care of the chimpanzees. We also thank S. Mori for helpful comments, and M. McAllister for help with manuscript editing. We would like to acknowledge partial support for the statistical analysis from the National Center for Research Resources and the National Center for Advancing Translational Sciences (NCATS) of the National Institutes of Health, and the statistician of the Johns Hopkins Biostatistics Center, A. Sanyal and C. Thompson. [^1]: **Competing Interests:**The authors have declared that no competing interests exist. [^2]: **Conceptualization:** TS.**Data curation:** TS MM.**Formal analysis:** TS KO.**Funding acquisition:** TS MM.**Investigation:** TS AM JS TM-N YH MT TM.**Methodology:** TS AM YH KO.**Project administration:** TS AM TM HO.**Resources:** TS AM JS MM TM-N YH MT TM.**Software:** TS.**Validation:** TS KO.**Visualization:** TS.**Writing -- original draft:** TS KO.**Writing -- review & editing:** TS AM JS TM-N YH HO KO.

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Photo Obese children who cut back on their sugar intake see improvements in their blood pressure, cholesterol readings and other markers of health after just 10 days, a rigorous new study found. The new research may help shed light on a question scientists have long debated: Is sugar itself harming health, or is the weight gain that comes from consuming sugary drinks and foods mainly what contributes to illness over the long term? In the new study, which was financed by the National Institutes of Health and published Tuesday in the journal Obesity, scientists designed a clinical experiment to attempt to answer this question. They removed foods with added sugar from a group of children’s diets and replaced them with other types of carbohydrates so that the subjects’ weight and overall calorie intake remained roughly the same. After 10 days, the children showed dramatic improvements, despite losing little or no weight. The findings add to the argument that all calories are not created equal, and they suggest that those from sugar are especially likely to contribute to Type 2 diabetes and other metabolic diseases, which are on the rise in children, said the study’s lead author, Dr. Robert Lustig, a pediatric endocrinologist at the Benioff Children’s Hospital of the University of California, San Francisco. “This paper says we can turn a child’s metabolic health around in 10 days without changing calories and without changing weight – just by taking the added sugars out of their diet,” he said. “From a clinical standpoint, from a health care standpoint, that’s very important.” Added sugars — the extra sweeteners food companies put in their products, not the sugar that occurs naturally in foods like fruit – are a topic of growing debate. In February, the federal government’s Dietary Guidelines Advisory Committee recommended that Americans limit their intake of added sugars to no more than 10 percent of daily calories. In 2014, the Food and Drug Administration proposed that food companies include a line on their nutrition labels listing the amount of added sugars in their products. After the dietary guidelines committee issued its report earlier this year, the agency expanded on its 2014 proposal, saying that companies should also list a “daily percent value” for added sugars on their labels in line with the 10 percent recommendation. The proposed changes have been strongly opposed by the food industry as unscientific. The Sugar Association, a trade group, said the F.D.A. was “making assertions that lack adequate scientific evidence,” and the Grocery Manufacturers Association criticized the standards the agency used to establish the daily value as being “inadequate.” The newly released study is timely in part because it lowered sugar intake among children to roughly 10 percent of daily calories, the amount recommended by the dietary guidelines committee. For their study, the scientists recruited 43 children between the ages of 9 and 18 who were considered at particularly high risk of diabetes and related disorders. All the subjects were black or Hispanic and obese, and had at least one or more symptoms of metabolic syndrome, a cluster of risk factors that includes hypertension, high blood sugar, abnormal cholesterol and excess body fat around the waist. On average, the subjects had been getting about 27 percent of their daily calories from sugar. By comparison, the average American takes in about 15 percent, though children typically consume much more than this in part because they have the highest intake of sugar-sweetened beverages. The study authors paired the subjects with dietitians. They then replaced the sugary foods in their diets with other foods purchased from local grocery stores. The goal was not to eliminate carbohydrates, but to reduce sugary foods and replace them with starchy foods without lowering body weight or calorie intake. “Wherever there was food with added sugar in their diets, we took it out and we replaced it with a no-added-sugar version,” Dr. Lustig said. So instead of yogurt sweetened with sugar, the children ate bagels. Instead of pastries, they were given baked potato chips. Instead of chicken teriyaki – which typically contains a lot of sugar – they ate turkey hot dogs or burgers for lunch. The remaining sugar in their diet came mostly from fresh fruit. Because the scientists were working on a tight N.I.H. budget, they could only carry out the costly intervention for nine days. But in that short space of time, they saw marked changes. On average, the subjects’ LDL cholesterol, the kind implicated in heart disease, fell by 10 points. Their diastolic blood pressure fell five points. Their triglycerides, a type of fat that travels in the blood and contributes to heart disease, dropped 33 points. And their fasting blood sugar and insulin levels – indicators of their diabetes risk – likewise markedly improved. One expert who was not involved in the new research, Dr. Frank Hu of the Harvard T.H. Chan School of Public Health, said that the study “strengthens the existing evidence on the relationship between added sugar intake and metabolic disease.” “This kind of study is very difficult to do,” he said. “But it provides a proof of concept that in a high risk population, reducing consumption of added sugar can have multiple metabolic benefits.” Dr. Sonia Caprio, a pediatric endocrinologist and professor of pediatrics at Yale Medical School, said that although the study was small, “it addressed the issue in an original way and tried to isolate the effect of sugar on metabolic syndrome and insulin resistance.” “This is an important area of research that might solve some of the metabolic issues that we are facing in children, particularly in adolescents,” she said. “This study needs to be taken seriously, and we need to expand on it.” Related: For more fitness, food and wellness news, “like” our Facebook page. 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Introduction {#Sec1} ============ When humans spread throughout the Earth, high-altitude environments presented a significant challenge to the people living within them. Low air pressure, hypoxia, strong solar radiation and low temperature exert great pressure on the survival of local people. Genetic factors in both the nuclear genome and mitochondrial DNA (mtDNA) genome play great roles in the adaptation to high-altitude environments, which was considered as natural impacts on human evolution and adaptation^[@CR1]^. In the past few years, an increasing number of genetic studies on the nuclear genome have shown that a series of genes have been involved in high-altitude adaptation in Tibetans^[@CR2]--[@CR8]^, Andeans^[@CR8],[@CR9]^ and Ethiopians^[@CR10],[@CR11]^, and these genes are mainly distributed in the hypoxia-inducible factor signaling pathway and the TP53 pathway. However, the role of the mtDNA genome in high-altitude adaptation are still in discussion and should receive more attention. Mitochondria are known as the cell's power plant, where cellular fuel is oxidized to provide energy for metabolism. Mitochondrial function is dependent on mtDNA, and mtDNA is well established as a genetic marker. A high mutation rate, small genome size, maternal inheritance, and lack of recombination make mtDNA an important tool for studying genetic structure in different populations. Besides, analyses of mtDNA sequences provide clues for exploring the genetic relationships between different populations, which contributes to deep understanding the role of mtDNA variations in human evolution. In addition to 2 rRNAs and 22 tRNAs, mtDNA encodes 13 core subunits related to oxidative phosphorylation (OXPHOS). Approximately 90% of the energy required by the cell is provided by OXPHOS, which is significantly affected by mtDNA variations. Hence, it is commonly believed that mtDNA contributed to high-altitude adaptation in high-altitude natives^[@CR12],[@CR13]^. There are three groups of high-altitude natives living in China, including high-altitude Tajiks (hereafter referred to as HA-Tajiks), Tibetans and Sherpas. The HA-Tajik population is one of 56 ethnic groups in China. HA-Tajiks have lived for generations in the Xinjiang Taxkorgan Tajik Autonomous County, where the average elevation is more than 4,000 m. Taxkorgan is perched in the highest part of the Pamirs. The world's second highest peak, Mount Qogir, towers over the south, and in the north stands Mount Muztagata, "the father of ice peaks." The HA-Tajik people seldom intermarry with other ethnic groups, and this ethnic identity means that their genetic structure shows little mixing with outsiders. Thus, it is attractive and feasible to explore the role of mtDNA in the high-altitude adaptation of HA-Tajiks. Tibetans are considered to be an ethnic group that is adapted to the high-altitude environment, and it has been reported that mtDNA variations influence the efficiency of oxygen utilization and function in native Tibetans^[@CR14]^. Sherpas live south of the Himalayas and are famous for their physical ability in climbing Mount Everest and are well-known as porters in the Himalayas. Their characteristics at high altitudes are considered as markers of high-altitude adaptation. Previous studies have found that eNOS, PPARA^[@CR15]^, HIF, ACE^[@CR16]^ and EPAS1 in the nuclear genome and CYTB, ATP6, ND1, ND4 and ND5 in the mtDNA genome play a great role in the high-altitude adaptation of Sherpas^[@CR17]^. Recently, a study analyzed mtDNA genomes in different populations in Central Asia located around the Pamirs^[@CR18]^, and different populations of Tajiks living at high altitude were also investigated. Because partial mtDNA sequences are not able to provide enough information, so complete mtDNA genome sequences were required for this research. To better understand the genetic structure of the mtDNA genome and identify the possible role of the mtDNA genome in high-altitude adaptation in HA-Tajiks, 80 HA-Tajik individuals living in Taxkorgan were enrolled, and their whole mtDNA genomes were sequenced. We also examined the mtDNA genomes of Tibetans and Sherpas as well as other reported Tajik populations^[@CR18]^ to compare the genetic differences between them and to analyze different patterns of high-altitude adaptation between three high-altitude native populations at the Qinghai-Tibetan Plateau and in the Pamirs from perspectives of mtDNA variations. Results {#Sec2} ======= Study population and reference population in this study {#Sec3} ------------------------------------------------------- A total of 11 populations, including 706 subjects, were analyzed in this study. The basic information of the subjects is listed in Table [1](#Tab1){ref-type="table"}.Table 1Basic information of the populations enrolled in this study.PopulationCategorySizeLocationSourceHigh-altitude TajikHighlander80Taxkorgan, Xinjiang, ChinaThis studySarikoli TajikHighlander86Taxkorgan, Xinjiang, ChinaReferenceWakhi TajikHighlander66Taxkorgan, Xinjiang, ChinaReferencePamirs TajikHighlander50Gorno-Badakhshan, TajikistanReferenceLowland TajikLowlander28Dushanbe, TajikistanReferenceEast Pamir KyrgyzHighlander68Taxkorgan, Xinjiang, ChinaReferenceLowland KyrgyzLowlander54Artux, Xinjiang, ChinaReferenceLowland UygurLowlander27Artux, Xinjiang, ChinaReferenceSherpaHighlander76Tibet, ChinaReferenceBeijing Han ChineseLowlander103Beijing, China1000 Genomes ProjectTibetanHighlander68Tibet, ChinaReference mtDNA genetic diversity of Tajiks {#Sec4} --------------------------------- The number of haplotypes, nucleotide diversity, haplotype diversity, Tajima's D and Fu's Fs were 73, 0.00216 ± 0.00024, 0.997 ± 0.00001, − 2.277 and − 33.741, respectively. The main frequencies of the haplogroups in the 80 HA-Tajiks analyzed in this study are shown in Fig. [1](#Fig1){ref-type="fig"}, and the major haplogroups were U, followed by H, T and J, indicating that the HA-Tajik population settled in Taxkorgan, China, may have originated from Europe^[@CR18],[@CR19]^. Haplogroup of each subject was provided in Table [S1](#MOESM1){ref-type="media"}. Phylogeny of 80 HA-Tajiks calculated by mtPhyl (version 5.003) was provided as dataset1 with a xlsx file. Detailed frequencies of haplogroups in 80 HA-Tajiks as well as other reference population were provided in Table [S2](#MOESM2){ref-type="media"}.Figure 1The haplogroup profiles of HA-Tajiks enrolled in this study. Major haplogroups were U, followed by H, T and J. Haplogroups were merged for brevity. Detailed frequencies of haplogroups in HA-Tajiks were listed in Table [S2](#MOESM2){ref-type="media"}. Bayesian skyline plot (BSP) for HA-Tajiks {#Sec5} ----------------------------------------- BSP was conducted to trace historical variations in population size based on coding regions of mtDNA genome (Fig. [2](#Fig2){ref-type="fig"}). Although the sample size of HA-Tajiks is small in this study, it could be inferred that the effective population size of HA-Tajiks is steadily growing, which is consistent with demographic data of HA-Tajiks in China, especially in recent years (<https://www.china.org.cn/e-groups/shaoshu/shao-2-tajik.htm>). Besides, the expansion of HA-Tajiks revealed by the BSP is also in accordance with the negative Tajima's D and Fu's Fs.Figure 2Bayesian Skyline Plot of HA-Tajik population history. BSP obtained by BEAST showed population history predicted from mitochondrial coding regions of 80 HA-Tajik subjects. The black line in the middle indicates the median population size predict from Bayesian posterior distribution. The population expansion may start from 10--15 kya before present. Genetic relationship of HA-Tajiks with other populations {#Sec6} -------------------------------------------------------- PCA was applied based on the frequencies of haplogroups in the mtDNA genomes to represent the relationships among the 11 populations enrolled in this study after transformation (Fig. [3](#Fig3){ref-type="fig"}). The detailed frequencies of the mtDNA haplogroups in the 11 populations are provided in Table [S2](#MOESM2){ref-type="media"}. Further analysis based on ARLEQUIN 3.5.1.3 and MEGA 7.0 also showed that the HA-Tajiks enrolled in this study presented a close genetic relationship with the Wakhi Tajiks, Pamiri Tajiks and Sarikoli Tajiks (Figs. [3](#Fig3){ref-type="fig"}, [4](#Fig4){ref-type="fig"}), indicating that they may belong to one nation, with differences in their geographical distributions. Moreover, Figs. [3](#Fig3){ref-type="fig"} and [4](#Fig4){ref-type="fig"} indicate that the genetic relationships of HA-Tajiks with Tibetans and Sherpas are distant, while Tibetans and Sherpas show a close relationship. Hence, it could be inferred that HA-Tajiks may exhibit a different pattern of high-altitude adaptation compared to Tibetans and Sherpas from the perspective of the mtDNA genome. To further explore these differences, a detailed comparison of different regions in the mtDNA genome between HA-Tajiks and Tibetans as well as Sherpas was performed in subsequent analysis.Figure 3PCA of populations from HA-Tajiks and other ten populations. PC map of populations based on mtDNA haplogroup frequencies (Table [S2](#MOESM2){ref-type="media"}). Figure 4Genetic distance of populations from HA-Tajiks and other ten populations based on mtDNA haplogroup frequencies. Different variations in the mtDNA genome between Tajiks, Tibetans and Sherpas {#Sec7} ----------------------------------------------------------------------------- After comparison to the rCRS, the number of variations in each polymorphism of the mtDNA genome was calculated in HA-Tajiks, Tibetans and Sherpas. Taking polymorphism 10400T of the mtDNA genome as an example, the numbers of variants were determined to be 6, 53 and 49, so the numbers of non-variants were 74, 15 and 27 in HA-Tajiks, Tibetans and Sherpas, respectively. At the statistical significance level of 0.025, our results indicated that there were significant differences in the distribution of many polymorphisms in the mtDNA genomes. As a result, only p values below 0.0000001 and polymorphisms in 13 genes belonging to the OXPHOS pathway encoded by the mtDNA genome are presented. The comparisons between HA-Tajiks and Tibetans and between HA-Tajiks and Sherpas are listed in Tables [2](#Tab2){ref-type="table"} and [3](#Tab3){ref-type="table"}, and the remaining results related to OXPHOS are provided in Table [S3](#MOESM3){ref-type="media"} and Table [S4](#MOESM4){ref-type="media"}.Table 2Results with p values below 0.0000001 in the comparison of the mtDNA genome between Tibetans and HA-Tajiks.PolymorphismsAmino acid changeRegionsTibetanHA-Tajiksχ^2^p valuesVariantNon-variantVariantNon-variant10400 TNoND3531567476.08\< 0.000000114783CNoCYTB531567476.08\< 0.000000115043ANoCYTB531577373.00\< 0.000000115301ANoCYTB531567476.08\< 0.0000001 Table 3Results with p values below 0.0000001 in the comparison of the mtDNA genome between Sherpas and HA-Tajiks.PolymorphismsAmino acid changeRegionsSherpaHA-Tajiksχ^2^p valuesvariantnon-variantvariantnon-variant3594TNoND1076404051.10\< 0.00000014104GNoND1076404051.10\< 0.00000014769GNoND2760423847.73\< 0.00000017028TNoCOX1751433742.71\< 0.00000017146GYesCOX1076404051.10\< 0.00000017256TNoCOX1373404041.40\< 0.00000018468TNoATP8076404051.10\< 0.00000018655TNoATP6076404051.10\< 0.00000018860GYesATP6760404051.10\< 0.000000110400TNoND3492767455.42\< 0.000000110664TNoND4L076404051.10\< 0.000000110688ANoND4L076404051.10\< 0.000000110810CNoND4076404051.10\< 0.000000110915CNoND4076404051.10\< 0.000000111719ANoND4751433742.71\< 0.000000113105GYesND5076404051.10\< 0.000000113276GYesND5076404051.10\< 0.000000113506TNoND5076404051.10\< 0.000000113650TNoND5076404051.10\< 0.000000114766TYesCYTB751433742.71\< 0.000000114783CNoCYTB492767455.42\< 0.000000115043ANoCYTB492777352.59\< 0.000000115301ANoCYTB492767455.42\< 0.000000115326GYesCYTB760404051.10\< 0.0000001 Table [2](#Tab2){ref-type="table"} showed that the frequencies of the variant polymorphisms 10400T, 14783C, 15043A and 15301A in Tibetans were significantly higher than those in Tajiks. Polymorphism 10400T belongs to ND3 and polymorphisms 14783C, 15043A and 15301A to CYTB. Hence, it seemed that polymorphisms in CYTB may provide more clues about high-altitude adaptation in Tibetans on the Qinghai-Tibetan Plateau than in HA-Tajiks in the Pamirs, and other regions of the mtDNA genome should be evaluated in relation to high-altitude adaptation in HA-Tajiks. Compared to Sherpas, HA-Tajiks exhibited more polymorphisms in multiple regions of the mtDNA genome, and detailed results are listed in Table [3](#Tab3){ref-type="table"}. The mtDNA genome of HA-Tajiks showed significant differences in ND1, ND2, COX1, ATP8, ATP6, ND3, ND4L, ND4, ND5 and CYTB, which are more complicated than the comparisons between Tajiks and Tibetans. Polymorphisms 14783C and 15301A of CYTB showed the most significant differences in the distribution between HA-Tajiks and Sherpas. In addition, it could also be inferred that Tibetans and Sherpas may present different patterns of high-altitude adaptation from the perspective of the mtDNA genome, because frequencies of certain variants in mtDNA genome also showed significant differences between Tibetans and Sherpas. Discussion {#Sec8} ========== This is the first study to compare and analyze molecular evidence of high-altitude adaptation in three high-altitude native groups from the perspective of the mitochondrial genome. In this study, the whole mtDNA genomes of 80 HA-Tajiks living in the Pamirs were sequenced, and the major mitochondrial haplogroups in HA-Tajiks were U, H and T as well as J confirmed that HA-Tajiks settled in the Pamirs were likely to be originated in Europe. BSP revealed by BEAST indicated that the effective population size was steadily increasing, which was in consistent with the current status of HA-Tajiks in China. Based on PCA and genetic distance analysis, we found that the HA-Tajiks enrolled in this study exhibited a close relationship with Wakhi Tajiks, Pamiri Tajiks and Sarikoli Tajiks. The difference in the mtDNA genome between HA-Tajiks and Sherpas was significantly greater than the differences between HA-Tajiks and Tibetans, suggesting different patterns of high-altitude adaptation were existed between HA-Tajiks, Tibetans and Sherpas. BSP was an effective tool to analyze population size based on mtDNA genome sequences. However, different settings of analysis methods would generate various results even dealing with the same sequences. Compared to Peng's research^[@CR18]^, significant decline in effective population size was observed by BSPs, which is conflict with negative Tajima's D and Fu's Fs yielded in his research. Possible explanations were different sample strategies, and mainly were attributed to different parameters of strict clock model and analysis methods. In Peng's research, this strict clock model was 1.404 × 10^−8^ substitutions per site per year and the TrN + I + G substitution model, and 2.308 × 10^−8^ substitutions per site per year as well as the GTR model of nucleotide substitution with empirical base frequencies were employed in this research. In addition, appropriate analytical methods are not easily determined when facing big data. Hence, parameters setting of software are not only depend on references but also in accordance to the actual situation as well as population history. Although HA-Tajiks, Tibetans and Sherpas are high-altitude natives, they exhibited great differences in their languages, customs and origins^[@CR18],[@CR20]^. Even after the long-term settlement of high-altitude environments, these three groups may show different responses to hypoxia stimulation at the molecular level, and variants in the mtDNA genome provided an useful tool for further analysis^[@CR1]^. Mitochondrion have been reported to be involved in high-altitude adaptation in Tibetans and Sherpas. The mitochondrial nt3010G-nt3970C haplotype^[@CR21]^ and haplogroup M9a1a1c1b in Tibetans^[@CR13],[@CR22]^ and haplogroups C4a3b1 and A4e3a in Sherpas^[@CR17]^ contributed to high-altitude adaptation. Compared to Tibetans, the distribution of polymorphisms 10400T, 14783C, 15043A and 15301A showed the most significant differences in Tajiks. However, the frequencies of these polymorphisms in Tajiks were significantly lower than those in Tibetans, indicating that other regions of the mtDNA genome should be considered in the assessment of the role of mtDNA in high-altitude adaptation in HA-Tajiks. Among the 13 genes belonging to the OXPHOS pathway, we found that the frequency of variant polymorphism 12372 (12372A) in ND5 was the most significantly increased compared to that in Tibetans (Table [S3](#MOESM3){ref-type="media"}). Taking U haplogroup as an example, 12372A is the marker of the U haplogroup, which accounted for the main lineage in the 80 HA-Tajiks enrolled in this study. Functional changes in 12372A were not detected, and this polymorphism showed no association with sudden infant death syndrome in the Swiss population^[@CR23]^. Although the 12372A variant in ND5 does not result in an amino acid change, it may affect the DNA-RNA network, mRNA stability, RNA splicing, translation kinetics and protein folding, etc.^[@CR15],[@CR24]^, which ultimately contributes to disease progression. It seems that many pathogenic mutations are enriched in the mtDNA genomes of high-altitude native peoples^[@CR13]^. However, these deleterious mutations do not induce a harmful phenotype in high-altitude natives, indicating that the diseases caused by mitochondrial mutations may be population specific. Hence, the role of 12372A in high-altitude adaptation in Tajiks needs to be reevaluated with larger samples, and the molecular mechanism associated with the 12372A mutation should be analyzed in further studies. In the comparison between Tajiks and Sherpas, the frequencies of polymorphisms 3594T and 4104G in ND1, 7146G and 7256T in COX1, 8468T in ATP8, 8655T in ATP6, 10664T and 10688A in ND4L, 10810C and 10915C in ND4, and 13105G, 13276G, 13506T and 13650T in ND5 were found to be significantly higher in Tajiks. In addition, these variants seemed to be in linkage disequilibrium. Except for polymorphisms 7146G, 13105G and 13276G, all other polymorphisms mentioned above did not induce amino acid changes. 7146G, 13105G and 13276G result in amino acid changes from threonine to alanine, isoleucine to valine and methionine to valine, respectively. However, genotype--phenotype association and functional analyses based on three nonsynonymous amino acid mutations have seldom been reported. The 7146G mutation was located in COX1, and this variant may influence the biogenesis of COX1 and ultimately cause a different response at the molecular level in Tajiks in the Pamirs compared with Sherpas on the Qinghai-Tibetan plateau, which needs to be checked through functional analysis. 13105G and 13276G in ND5 were found to be associated with a risk of cervical cancer^[@CR25]^. ND5 is a primary subunit of nicotinamide adenine dinucleotides, and a mutation in ND5 can induce higher levels of reactive oxygen species^[@CR26]^. Combined with 13506T and 13650T in ND5, it seemed that alterations in ND5 would induce cumulative effects and may play a great role in high-altitude adaptation in Tajiks. However, the functional significance and the underlying mechanisms are unknown. Further investigations including molecular and biochemical studies are needed to explore the role of mutations in ND5 in high-altitude adaptation in HA-Tajiks. With the development of DNA sequencing technologies, next-generation sequencing has been widely applied in genetic studies, and the accuracy has increased significantly. Traditional Sanger sequencing based on PCR products was performed in this study, and we found that checking DNA sequencing results and the assembly of DNA fragments manually is highly time and energy consuming. Hence, in the acquisition of whole mtDNA genomes, next-generation sequencing should be considered as the main tool in further analysis, and Sanger sequencing could be a powerful additional complement, especially when the results acquired by next-generation sequencing are ambiguous. Conclusion {#Sec9} ========== We found that the lineages including U, H, T and J accounted for most HA-Tajik samples, indicating an European origin, and the HA-Tajik population showed a closer relationship with Wakhi Tajiks. BSP revealed by BEAST indicated that the effective population size was steadily increasing. Among 13 genes belonging to the OXPHOS pathway encoded by the mtDNA genome, HA-Tajiks showed the most significant differences in ND3 and CYTB compared to Tibetans. Compared to Sherpas, HA-Tajiks showed the most significant differences in ND1, ND2, COX1, ATP8, ATP6, ND3, ND4L, ND4, ND5 and CYTB. The associated biochemical changes and molecular mechanisms should be explored by functional investigations in further studies. Materials and methods {#Sec10} ===================== Ethics statements {#Sec11} ----------------- This research was approved by the ethics committee of the Third Military Medical University and the 950th Hospital of the PLA of China. All experiments were performed in accordance with relevant guidelines and regulations. All participants provided written informed consent before this investigation commenced. Study population {#Sec12} ---------------- A total of 80 unrelated HA-Tajiks (19 males, 52.9 ± 14.9 years, 19--76 years old; 61 females, 46.0 ± 15.0 years, 25--83 years old) were enrolled in this study. All subjects confirmed that they and their parents had been born and lived in Taxkorgan their whole lives in a questionnaire. Genomic DNA was extracted from venous blood using a DNA isolation kit (Omega Bio-Tek, Inc., Norcross, GA, USA) and was stored at − 20 °C for further use. mtDNA genome amplification and sequencing {#Sec13} ----------------------------------------- Eight pairs of primers were applied to amplify the mtDNA genome by polymerase chain reaction (PCR), and 22 primers were used for sequencing the PCR products^[@CR26]^ by Sanger dideoxy sequencing (detailed information of PCR amplification and sequencing primers is listed in Table [S5](#MOESM5){ref-type="media"} and [S6](#MOESM6){ref-type="media"}). The sequence of every PCR product was carefully checked according to the revised Cambridge Reference Sequence (rCRS) (GenBank: NC_012920). All of the sequences of the PCR products from each subject were integrated, and overlapping sequences were removed. After manual check of sequence diagrams, we found that the sequencing accuracy of 315--598 in sample 106, 120, 122, 133, 148, 149, 156, 167, 304, 320, and 16190--16396 in sample 119, 138, 225 were not satisfactory because of poly C structure existed. To make our work more convincing, we delete the mtDNA sequences in 315--598 and 16190--16396 belonging to D-loop region in samples mentioned above respectively, and these sequences were replaced as sequencing gaps. Finally, we obtained the mitochondrial genome sequence of 80 HA-Tajiks without 315--598 or 16189--16396 belonging to D-loop region for the following analysis. mtDNA haplogroup analysis and reference mtDNA genomes {#Sec14} ----------------------------------------------------- Each mtDNA genome of 80 HA-Tajik individuals was compared to Phylotree 17 rCRS to confirm variant sites and haplogroup by using Mitotool (<https://mitotool.kiz.ac.cn/)>^[@CR27]^ Ten additional populations living in East Asia and Central Asia, including Tibetans and Sherpas, were selected as references. The GenBank identification numbers of the Tibetans and Sherpas are provided as supplementary materials in Table [S7](#MOESM7){ref-type="media"}. Sequence data for the mtDNA genome were acquired from the 1000 Genomes Project or downloaded from GenBank as the references indicate. Variant sites and haplogroups were also acquired by using Mitotool as mentioned above. All the mtDNA sequences of 80 HA-Tajiks as mentioned above were deposited in Genbank (MT554196-MT554275). Analysis of mtDNA genomes {#Sec15} ------------------------- The mtDNA genetic diversity of HA-Tajiks (including haplotype numbers, nucleotide and haplotype diversity, Tajima's D, and Fu's Fs) was calculated by DnaSP6.0^[@CR28]^. The genetic distances between the HA-Tajiks and the reference populations based on the mtDNA genomes were analyzed by PCA based on the haplogroup distributions in different populations after normalized transformation^[@CR29]^. The Fst values between the populations enrolled in this study were calculated with ARLEQUIN 3.5.1.3^[@CR30]^. A phylogenetic tree was constructed with a neighbor-joining tree with MEGA 7.0. The phylogeny was constructed by using mtPhyl^[@CR31]^ (<https://sites.google.com/site/mtphyl/home>) with 80 complete mtDNA sequences in HA-Tajiks. The variants located in regions 16519, 16180--16193 and 310--315 and the AC indels in regions 515--522 were not included in the subsequent analysis^[@CR18]^. Bayesian phylogenetic analysis of HA-Tajiks {#Sec16} ------------------------------------------- The Bayesian skyline plots (BSPs) for HA-Tajiks were performed by BEAST v1.7.5. mtDNA coding region (np 577--16024) of each HA-Tajik subject was acquired by comparison of rCRS. After alignment of 80 mitochondrial coding region sequences, we employed the GTR model of nucleotide substitution with empirical base frequencies, and selected a strict clock model with the rate of 2.038 × 10^--8^ subs/site/year^[@CR32]^. Markov chain Monte Carlo (MVMV) was applied to estimate coalescent history. Parameters of MVMV were set as running for 400,000,000 generations and calculated every 4,000 generations. Results yielded by BEAST were visualized by Tracer 1.5 (<https://tree.bio.ed.ac.uk/software/tracer/>). Detailed differences in the mtDNA genomes between Tajiks, Tibetans and Sherpas {#Sec17} ------------------------------------------------------------------------------ To further identify the differences between HA-Tajiks, Tibetans and Sherpas, their whole-mtDNA-genome sequences were compared to the rCRS to confirm the variants in the mtDNA genomes in detail. The number of variants in different regions of the mtDNA genome was calculated by direct counting, and the variant distributions in different regions were analyzed by the chi-square test, which may reveal different patterns of high-altitude adaptation among HA-Tajiks, Tibetans and Sherpas. For the chi-square test, a Bonferroni correction was applied for multiple tests. Because the number of comparisons was 2 (HA-Tajik vs Tibetan, HA-Tajik vs Sherpa), the statistical significance level was set at 0.05/2 (0.025), and all p values were two-tailed. Supplementary information ========================= {#Sec18} Supplementary Table 1. Supplementary Table 2. Supplementary Table 3. Supplementary Table 4. Supplementary Table 5. Supplementary Table 6. Supplementary Table 7. Supplementary information. **Publisher\'s note** Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Supplementary information ========================= is available for this paper at 10.1038/s41598-020-67519-z. This work was supported by the second Tibetan Plateau Scientific Expedition and Research Program (STEP), Grant No. 2019QZKK0607, Key Project of the Logistics Research Program, PLA (BLJ18J005) and the National Natural Science Foundation of China (81571843). We also appreciate the assistance in the data analysis from Dr. Liyuchun in the State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, China. Y.C. and Y.J.L. conceived and designed study concept. Y.C., L.G., X.Y.L. and X.S.C. collected the samples and performed the experiments. Y.C. analyzed the data. Y.C. drafted the manuscript. S.H.Y. and Y.J.L. provided critical revisions. All authors approved the final version of the manuscript for submission. The authors used mitochondrial sequence data in Genbank, all the sequence data could be downloaded as Genbank number indicating from National Center of Biotechnology Information. All other relevant data are provided in the paper and Supporting files. The authors declare no competing interests.

3

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Q: Literal Assignment in Java what's the difference in defining double example = 23.1d or double example = 23.1 Why long, float and double can end with l, f, d? A: There is no difference between double example = 23.1d; and double example = 23.1; because a floating point literal without a type suffix is always interpreted as a double. The type suffixes are necessary in order to avoid ambiguities in certain scenarios. For example, java supports method overloading. This means that you can have void x( float f ); and void x( double d ); Both methods are called x; which one will be selected depends on the type that you pass; if you pass a variable which is already known to be either float or double, things are clear; but if you want to pass a literal, like this: x( 5 ); then you have to be able to specify whether you mean this 5 to be a float or a double, so as to select the right method. There are a few other very nuanced situations where the type of the literal matters. For example, the following code: System.out.println( "" + (2/3.3333) ); System.out.println( "" + (2/3.3333f) ); Yields the following output: 0.6000060000600006 0.600006 ...because the first number is a double, while the second number is a float. Similar disambiguation concerns make the "L" type suffix necessary for long integer literals.

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Stretchable electronics, an emerging class of modern electronic materials that can bend and stretch, have the potential to be used in a wide range of applications, including wearable electronics, "smart skins" and minimally invasive biomedical devices that can move with the body. Today's conventional inorganic electronic devices are brittle, and while they have a certain flexibility achieved using ultrathin layers of inorganic materials, these devices are either flexible, meaning they can be bent, or they are stretchable, containing a discrete LED chip interconnected with stretchable electrodes. But they lack "intrinsic stretchabilty," in which every part of the device is stretchable. Now, researchers at the UCLA Henry Samueli School of Engineering and Applied Science have demonstrated for the first time an intrinsically stretchable polymer light-emitting device. They developed a simple process to fabricate the transparent devices using single-walled carbon nanotube polymer composite electrodes. The interpenetrating networks of nanotubes and the polymer matrix in the surface layer of the composites lead to low sheet resistance, high transparency, high compliance and low surface roughness. The metal-free devices can be linearly stretched up to 45 percent and the composite electrodes can be reversibly stretched by up to 50 percent with little change in sheet resistance. Because the devices are fabricated by roll lamination of two composite electrodes that sandwich an emissive polymer layer, they uniquely combine mechanical robustness and the ability for large-strain deformation, due to the shape-memory property of the composite electrodes. This development will provide a new direction for the field of stretchable electronics. This research was recently published in the peer-reviewed journal Advanced Materials . Explore further UCLA engineers create new transparent electrodes for highly flexible electronics

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Curriculum Bank Lesson searchable by grade and subject. Often include videos Gooru is a search engine for learning that allows you to explore and study over 2,600 standards-aligned and personalized study guides. Study guides cover 5th-12th grade math and science topics, and resources include digital textbooks, animations, instructor videos and more. All resources are vetted and organized by teachers or Gooru’s content experts, so you don’t have to sort through the mess of subpar educational resources available online yourself. Learn Zillions Math videos for grades 3-9. Created by teachers. Option to create playlists for individual students and assessments. Mathtrain.TVThese video math tutorials were created for students by students from Lincoln Middle School (Santa Monica, CA). Sixth graders have created nearly one hundred clips, most of them less than two minutes in run time. NuskoolThis is a site that uses pop culture as teaching moments for students. Tailored to grades 6th-12th students learn a variety of subjects such as: Math, Science, English, etc through educational lessons based on the different elements of pop culture (video games, sports, films, etc.). Math Liveis a neat mathematics website hosted byLearn Alberta. Math Live presents students with animated stories that teach mathematics lessons. In all there are twenty-three lessons for elementary school and middle school students. The lessons are divided into four categories; Number, Patterns and Relations, Shape and Space, Statistics and Probability. Each animated lesson is accompanied by a mathematics worksheet that students complete either while watching the lesson or after viewing the lesson. Each lesson is divided into sections and students can advance or rewind as needed. mySkillBoard is a nice new site for differentiating instruction. The way this is done is by an educator inputing student data into mySkillBoard and then being able to assess students through different visualizations. Also, an educator can align student skills to Common Core Standards and even use it on any mobile device. PBS Math Clubis a YouTube channel in which students can watch and interact with math videos. Each of the videos contains a series of math lessons and challenge activities. To complete a challenge students click on the video to answer questions. If they answer correctly, they move on to the next question. If they answer incorrectly students are shown another video clip that explains the correct answer. LearnBop- A great site for educators teaching Math in grades K-12 that tracks student progress and allows educators to differentiate instruction.Math Is Power 4 U. Math Is Power 4 U is a large collection of tutorial videos primarily covering topics found in middle school and high school math courses. The videos are short and direct. You could make very similar videos yourself, if you wanted to. The best aspect of Math Is Power 4 U is the searchable database of videos. The database, hosted by Phoenix College, makes it easy to quickly find a video explaining topics in arithmetic, algebra, geometry, calculus, and half a dozen other topics. MathsMastervideos on a range of topics. See videos about the basic four operations up to complex algebra graphs. Each video is presented in a slow, step by step,student friendly way. These videos are great as an introduction to a topic or forhome study. Plus Magazineis an internet magazine which aims to introduce readers to the beauty and the practical applications of mathematics. Plus provides articles and podcasts on any aspect of mathematics and it also features review of math books and well as challenging math puzzles. Knewton.The company believes its new, free online tutoring platform will radically transform how teachers personalize instruction. Knewton claims to offer automated, digital tutoring that responds to each student's needs. "We can take the combined data power of millions of students — all the people who are just like you — [who] had to learn a particular concept before, that you have to learn today — to find the best pieces of content, proven most effective for people just like you, and give that to you every single time," he says. Here's how it works: The platform presents video and a variety of written content and then asks multiple-choice questions. Based on student responses, and patterns of responses from other, similar students, the next piece of content is served up. ModMath ( app) is an adaptive program that improves math skills. The app lets you type math problems right onto the touch screen of an iPad rather than write them out long-hand. You can then solve the problems using the touch pad and print or e-mail the assignments all without ever picking up a pencil. Prodigy- A free online Math game aligned to Common Core Standards grades 1-6th. Best of all this game differentiates instruction and educators can track students' progress as well as generate detailed reports. Sports Science - Awesome collection of short videos that will engage kids in science and math from the people at ESPN.ScootPad is a math and reading practice platform for elementary grades (K-5). Self-paced and personalized practice on ScootPad keeps kids engaged & challenged. ScootPad is Free. Buzz Mathis the latest interactive math workbook which provides middle school students with immediate detailed feedback, examples, and motivation to allow them to progress at their own pace. Motion Math Gamesdesigns challenging math games to sharpen your kids mathematical wits. It also has a mobile version to install on your iPad. IXL - One of the most popular sites around for Math that allows for student tracking w/ detailed reporting. Also, w/ the ability to track student "trouble" areas a teacher can adjust their teaching to help meet the needs of their students. iPracticeMathis a site for educators or students looking to teach, learn, or reinforce their math skills. Geared towards K-12, iPracticeMath covers a wide variety of subjects such as: Geometry, Algebra, Fractions, etc. Also, iPM has an abundance of resources for educators/students to use such as: worksheets, problem walkthroughs, glossary, and more. Best of all a registered educator/parent can get detailed reporting and track student progres Exampl : Get unstuck with homework Get instant homework help with Exampl! Take a photo of your problem to get help from your peers. You can even annotate your question, add a voice note, and tag it with a specific subject, like Algebra. Once your question has been solved, you can help other students too! No more typing elaborate solutions when you help others. It takes another photo or annotation to help others. KnowRe is a site for learning Math. Students can learn at their own pace and earn rewards such as digital badges for accomplishments. A nice feature for teachers is that is is aligned to common core standards and teacher can track and get real-time results on student data.XtraMath Its goal is to develop effective, efficient, adaptive and intrinsically rewarding supplemental math activities and make them available for free. myMathUniverse (gr 5-8) site with videos to help students with math homework and challenge them with new problemsmyMathUniverse. Supports middle grades math program, digits, a curriculum written entirely to the Common Core State Standards (CCSS) which leverages technology to personalize student learning and optimize class instructional time. Manga High, a collection of casual online math games developed using the Japanese manga style of animation Virtual Nerd, which lets students choose their own path through math content with step-by-step tutorials and a dynamic whiteboard Media 4 Math has a nice regular feature called Math in the News. Math in the News offers ideas for short mathematics lessons based on current news stories. TenMarks - A common core aligned program for Math (grades 1st-10th) that uses differentiated instruction to help students learn. Math Live presents students with animated stories that teach mathematics lessons. In all there are twenty-three lessons for elementary school and middle school students. The lessons are divided into four categories; Number, Patterns and Relations, Shape and Space, Statistics and Probability. Each animated lesson is accompanied by a mathematics worksheet that students complete either while watching the lesson or after viewing the lesson. Each lesson is divided into sections and students can advance or rewind as needed. Buzz Math is not a completely free to use tool, but they do have a free option that makes it worth checking out! Right now, you can subscribe one class for free for the school edition of Buzz Math. Buzz Math is intended for students in Middle School math. All of the activities are directly tied to Common Core Standards. You can assign activities based on a specific standard for the whole class, or just assign the activity to individual students. You get feedback immediately as students complete an activity so that you can plan instruction accordingly. These are not your typical math site activities (online multiple choice). Instead, each activity is a little different, highly engaging, and provides students with great feedback. Gummii - An innovative site (private alpha)/app for different areas of Math (fractions, addition, subtraction). Gummi immerses students into a educational 3D world (similar to Minecraft) where they solve mathematical equations tailored to differentiated instruction. 101 Questionson which he is sharing images and videos as prompts for developing math questions. TenMarksoffers a free online mathematics program designed to supplement your in-classroom mathematics instruction. The free TenMarks program covers materials for students in grades two through ten. In the program there are more than 2,000 video lessons available to students to view on demand. Teachers can use the TenMarks program to assign lessons and problems to individual students or to an entire class. Teachers can track the progress of individual students and the progress of an entire class. Yummy Math is a website designed for the purpose of sharing mathematics problems and scenarios based on things happening in the world today. For example, the activity for December 4th was based on Lebron James's return to Cleveland. Yummy Math lists activities chronologically as well as by mathematics subject area. Two mathematics teachers, Brian Marks and Leslie Lewis, developed Yummy Math and welcome suggestions from other mathematics teachers. Math PickleA nice site for locating videos and exercises appropriate for teaching a variety of mathematics concepts at a variety of grade levels. When you visit Math Pickle you can browse for videos by grade level. Once you've selected a grade level you can then refine your browsing to a particular concept. Each concept has a demonstration video and links to Keynote and Powerpoint files for teachers. Each concept also has links to PDF worksheets that you can download and print. MathVidsath videos about tough Math concepts starting with pre-algebra through high school math Desmos includes support for graphics, photos, math tools, and interactive lessons. You can create math lesson using the math tools, including graphing and equations. You can also the graphics program to create interactive diagrams where students can move the labels themselves. Math Open Reference is a free online reference for geometry teachers and students. It features animated and interactive drawings to demonstrate geometry terms and concepts. The table of contents is divided into four basic categories; plane geometry, coordinate geometry, solid geometry, and function explorer tools. Click on any subject in the first three categories to find definitions, examples, and interactive drawings. In the function explorer category users can select linear functions, quadratic functions, or cubic functions to explore how changes in variables affect the graphed output. Manipulatives Math Tool Chest- fun math interactives for any kid Useful for smartboards also PBS Learning Media has a free service called Learning Media. Resources include pictures, video and interactive materials from a robust library of high-quality digital content from PBS, and a growing list of other contributors including the National Archives, Library of Congress and NPR. There are research-based resources, including videos, interactives, images, audio files and lesson plans. You can view three resources. Then you have to create an account which is free. Can be filtered by grade level (Pre-K to 12+), subject (8), media type (document, audio, video, etc.), language (5) and accessibility (text, audio description, display transformation, etc). Audacity This site provides a nice set of maths tools for whiteboards. Whilemost whiteboard software have these tools, can you ever find themwhen you want them? Another benefit of this resource is that this will work on any Pattern Maker Looking for a way to help your students build their spatial sense? Pattern Maker – a special combination of art and geometry -- might be just the right tool for you. Students can flip, slide, turn, scale, and tessellate colorful objects, creating patterns of their own imagination or copying pre-selected patterns. Finishing a pattern triggers a brief question for the student to answer, based on the geometric techniques used and linked to key terms in a Shape Dictionary. Mangahighcreates exceptionally high-quality, game-based learning resources to help Primary and Secondary students reinforce their Mathematics skills in a way that is both fun and engaging. In addition to all the great resources, the service includes assessment and analytical tools that enable teachers to monitor the progress of individual students. Best of all, these activities also work great on the SMART Board Interactive Whiteboard. Calendar Clowns(gr. 1-3) Games teaches how to navigate a calendarRounding Master(gr. 2-5)Rounding off game in a Who Wants to be A Millionaire formatGarage Sale Wizard (gr 1-3) You play the role of a cranky old man trying to make a few bucks by selling his stuff at a garage sale. For each item, there will be three people vying for its purchase. Each person will offer a different amount of money. Count up the coins and click on the person who offers the best deal (the most money). Charts Graphmaster - Graph Master is a program is a one-of-a-kind program that allows students to create three different interactive, printable graphs on one screen based on data collected in a survey or poll of their classmates. What makes Graph Master so useful, however, is the fact that after students make their graphs, the program asks them eight multiple choice questions about their graphs using the inputted data. Hohli Online Charts Builderis a nice tool for creating a variety of charts for online display. Using the Hohli Online Charts Builder you can create bar graphs, line graphs, pie charts, Venn diagrams, scatter plots, and radar charts. Your chart will be generated as you enter information so that you can see how each piece of information influences the chart. When you're satisfied with your chart just click on it to save it to your computer or to grab the embed code to use on your blog or website. Because the charts update as each new piece of data is added, students will be able to see how each data set they add affects their chart's display. Cacoo- Nice site for creating online charts and graphs with a built-in chat feature for collaboration. Plus Magazine is a free online publication dedicated to introducing readers to practical applications of mathematics. Plus Magazine strives to reach that goal through the publication of mathematics-related news articles, podcasts, and mathematics puzzles designed around "real-life" scenarios. Gooruis a service that aims to provide teachers and students with an extensive collection of videos, interactive displays, documents, diagrams, and quizzes for learning about topics in math and science. Access to hundreds of resources according to subject areas such as chemistry, biology, ecology, algebra, calculus, and more. Within each subject area you can look for resources according to media type such as video, interactive display, slides, text, and lesson plans. Dynamic Paper Need a pentagonal pyramid that's six inches tall? Or a number line that goes from 18 to 32 by 5's Or a set of pattern blocks where all shapes have one-inch sides? You can create all those things and more with the Dynamic Paper tool. Place the images you want, then export it as a PDF activity sheet for your students or as a JPEG image for use in other applications or on the web. Mathematics in Moviesis a website developed by Oliver Knill, a Harvard Mathematics professor. Mathematics in Movies is a collection of video clips from popular movies and television shows in which references to mathematics are made. One clip that I enjoyed comes from an episode of The Office in which Oscar tries to explain the concept of a budget surplus to Michael. Study Jams is a Scholastic website designed to help elementary school students learn and review math and science information through songs and videos. To use Study Jams students search for a topic in the math or science category. Each Study Jam offers a short tutorial on that topic in the form of a video, slideshow, or song. When there is a song available Study Jams provides a karaoke format for kids to sing along if they like. EaselAlgebra ilite - Easel combines interactive, hands-on algebra workbooks with instant "ShowMe" lessons. If you get stuck on a problem, just tap "ShowMe" and see a step-by-step animation of how to solve the problem. Algebra 4 All A social network dedicated to algebra teachers. At Algebra 4 All (A4A), teachers support one another in the practice of teaching algebra Math Open Reference is a free online reference for geometry teachers and students. Math Open Reference features animated and interactive drawings to demonstrate geometry terms and concepts. The table of contents on Math Open Reference is divided into four basic categories; plane geometry, coordinate geometry, solid geometry, and function explorer tools.

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Q: Break if statement in python i have mistake with my python code. There's mini game about guessing code. i want to break if statements and make else statement (activated when i guess wrong letter).Here's the code. Return and break function outputs: "return/break function outside the loop". Please, modify the code :D ` import time print('Oto jest gra, w której musisz odgadnąć kod! Kod ma 4 litery!') decyzja = input('Chcesz grać? T/N\n') if decyzja == "t" or "T": one = input('Wpisz 1 litere\n') if one == "k": two = input('Wpisz 2 Litere\n') if two == "u": three = input('Wpisz 3 litere\n') if three == "b": four = input('Ostatnia!\n') if four == "a": time.sleep(2) print('Zgadles kod!!!') ` A: Try this (it's better to use a function): import time def numguess(myinput): if decyzja.lower() == "t": one = input('Wpisz 1 litere\n') else: return False if one == "k": two = input('Wpisz 2 Litere\n') else: return False if two == "u": three = input('Wpisz 3 litere\n') else: return False if three == "b": four = input('Ostatnia!\n') else: return False if four == "a": time.sleep(2) print('Zgadles kod!!!') else: return False print('Oto jest gra, w której musisz odgadnąć kod! Kod ma 4 litery!') decyzja = input('Chcesz grać? T/N\n') numguess(decyzja)

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Electrical circuits requiring high power handling capability (>20 watts) while operating at high frequencies such as radio frequencies (500 MHz), S-band (3 GHz) and X-band (10 GHz) have in recent years become more prevalent. Because of the increase in high power, high frequency circuits there has been a corresponding increase in demand for transistors which are capable of reliably operating at radio frequencies and above while still being capable of handling higher power loads. To provide increased power handling capabilities, transistors with a larger effective area have been developed. However, as the area of a transistor increases, the transistor, typically, becomes less suitable for high frequency operations. One technique for increasing the area of a transistor while still providing for high frequency operations is to use a plurality of transistor cells that are connected in parallel. Such may be provided using a plurality of gate fingers, thus, the source to drain distance may be kept relatively small while still providing for increased power handling capability. Conventionally, when a plurality of parallel transistor cells are connected in parallel on a single chip, the cells are evenly spaced such that the gate-to-gate distance between adjacent cells (referred to herein as “pitch” or “gate pitch”) is uniform. When such multi-cell transistors are used in high frequency operations, they may generate a large amount of heat. As a device heats up, performance of the device typically degrades. Such degradation may be seen in gain, linearity and/or reliability. Thus, efforts have been made to keep junction temperatures of the transistors below a peak operating temperature. Typically, heatsinks and/or fans have been used to keep the devices cool so as to ensure proper function and reliability. However, cooling systems may be increase size, electrical consumption, costs and/or operating costs of systems employing such transistors. With uniform pitch multi-cell transistors, the temperature of cells near the center of the array are typically greater than those of the cells at the periphery. This is generally the case because the cells at the periphery have a larger area and/or a greater thermal gradient to areas surrounding the cells. Thus, for example, adjacent cells near the center of the multi-cell array will each generate heat and thus, each side of the cells will be at an elevated temperature with respect to cells farther from the center. This results in a thermal profile that is roughly a bell curve with center junction temperatures being the hottest and with the outer most junctions having a substantially reduced operating temperature compared to the center junctions. An uneven temperature distribution among the junctions of a device may reduce device linearity. For example, for a device with a plurality of evenly spaced gate fingers connected by a manifold, RF phasing errors may occur along both the gate manifold and the individual gate fingers as a result of differing gate resistance as a function of temperature. Conventionally, to address these issues the spacing between the gate fingers is widened and/or the length of the fingers are shortened and additional fingers added to achieve the same net active area. Both of these solutions may result in spreading the heat load generated in the center of the device over a wider area. These solutions also may result in a larger area for the multi-cell transistor that may reduce the number of die per wafer.

3.296875

3

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Q: How to identify Enantiomers AP Biology Question So I know that enantiomers are like mirror images of each other, but not identical (superimposable) upon one another. On Wikipedia, I read that it was like our hands, similar but not identical (you can't rotate one hand into another. Makes sense. But I'm not sure how this would help me identify the enantiomers. All the molecules look identical. The answer is (D). What is different about D? A: The key point is that for four of the five pairs, the structure on the left can be rotated to make a structure exactly like the one on the right. For example, the left structure in (A), if rotated 120° about the C-CO$_2$H bond, is equivalent to the structure on the right. For two "enantiomeric" structures, it is not possible to do this. It might be helpful to draw every possible rotation of the structures in (D), to see that it is impossible to produce the structure on the right by rotating the one on the left.

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One goal of semiconductor fabrication is to increase the density of active elements provided on an integrated circuit. In order to accomplish this, ongoing investigation in advanced lithography is underway to decrease the critical dimensions of active elements used to form these integrated circuits. Current lithography uses energy sources that include i-line at 365 nanometers and deep ultra-violet (DUV) at 248 nanometers to pattern substrate features. Decreasing the wavelength of the energy source allows for the formation of photoresist features having smaller critical dimensions. Accordingly, smaller wavelength energy sources are being developed as alternatives to conventional lithography. These include x-ray, ion projection, extreme ultra-violet (EUV) at 13.4 nanometers, and scattering with angular limited projection in electron-beam lithography (SCALPEL). SCALPEL and x-ray lithography masks are formed of attenuating elements overlying thin membranes. The membrane thickness of a SCALPEL mask is typically in range of 100-150 nanometers and the membrane thickness of an x-ray ray mask is typically in a range of 2000-5000 nanometers. Cleaning such masks is relatively difficult and presents numerous problems. Conventional wet chemical processes do not adequately remove particles without reacting with or damaging the mask. Physical agitation, such as ultrasonic agitation, is generally undesirable because of the delicate nature of the membranes. Other cleaning techniques, such as dry laser cleaning and frozen ice cleaning, are likely to be ineffective at adequately cleaning the masks, particularly when attempting to remove particles between patterned mask features. Conventional lithography has adopted the use of pellicles to protect masks from particles and to prevent the imaging of defects onto the semiconductor substrate. However, the use of pellicles in SCALPEL and x-ray lithography is problematic. The pellicle increases the thickness of material through which the energy must pass, thereby reducing throughput and increasing chromatic aberration. Additionally, contaminants or particles deposited on pellicles used in SCALPEL and x-ray lithography may nevertheless be imaged onto the resist, unlike in conventional lithography. Development in the field of self-assembled monolayers (SAMs) has been underway for several years. The particularities of commonly formed SAMs are disclosed in technical literature, including "Formation and Structure of Self-Assembled Monolayers", by Abraham Ulman, Chemical Reviews, Vol 96, 4, (1996) 1532-1544, and "An Introduction to Ultrathin Organic Films: From Langmuir-Blodgett to Self-Assembly" by Abraham Ulman, Academic Press, Inc., Boston (1991) 237-304, both of which are hereby incorporated by reference.

3.046875

3

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• The ExoMars Schiaparelli Lander (Entry, Descent, and landing Module, or EDM) crashed on the Martian surface on 19 October 2016. Also on that day the Trace Gas Orbiter successfully entered Mars orbit. The HiRISE images acquired soon after the crash showed diffuse dark markings surrounding a shallow crater, plus small bright spots. HiRISE re-imaged this location on 25 March 2019, while dust was still settling from the planet-encircling dust storm, so surface features had low contrast.HiRISE re-imaged this spot again through a much clearer atmosphere on 14 December 2019 ( see animation ). Much of the diffuse dark material has faded, perhaps from dust fallout, such that the crater is now more distinct. At least two bright spots are still visible.In 2020 we expect three launches to Mars leading to landing attempts in early 2021: NASA’s unnamed (Mars 2020) rover, that will collect samples for return to Earth; the ESA/Roscosmos ExoMars lander and Rosalind Franklin rover; and an orbiter, lander, and Huoxing-1 (Mars-1) rover from China. HiRISE will be ready to see what happens.Written by: Alfred McEwen (29 January 2020)

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Contents >> Leading Causes of Death >> Overview - Leading Causes of Death OVERVIEW Ranking causes of death is a useful method of describing patterns of mortality in a population. It allows comparison over time and between populations. However, different methods of grouping causes of death can result in a vastly different list of leading causes for any given population. For this reason ABS ranks leading causes of death in this publication based on research presented in the Bulletin of the World Health Organization, Volume 84, Number 4, April 2006, 297-304 . For further information see Explanatory Notes 41-43. In 2011, the leading underlying cause of death for all Australians was Ischaemic heart disease (I20-I25), which includes angina, blocked arteries of the heart and heart attacks. Ischaemic heart diseases were identified as the underlying cause of 21,513 deaths, 14.6% of all deaths registered in 2011. While Ischaemic heart diseases have been the leading cause of death in Australia since 2000, the proportion of deaths due to this cause has decreased, from 19.5% (26,063) in 2002 to 14.6% (21,513) in 2011. Cerebrovascular diseases (I60-I69) have remained the second leading underlying cause of death in 2011. Cerebrovascular diseases include haemorrhages, strokes, infarctions and blocked arteries of the brain. Over the last 10 years, deaths due to this cause have decreased by 10.2%, from 12,533 deaths in 2002 to 11,251 deaths in 2011. Dementia and Alzheimer's disease (F01, F03, G30) was the third leading cause of death in 2011. The number of deaths due to this cause has increased by 126% over the past decade from 4,364 in 2002 to 9,864 in 2011. This is largely due to an increase in deaths due to Dementia (F01, F03), which increased from 2,513 in 2002 to 6,877 in 2011. For further information see Explanatory Note 84. Trachea, bronchus and lung cancers (C33-C34) were the fourth leading cause of death in 2011. Over the last 10 years, deaths due to this cause have increased by 11.1%, from 7,303 in 2002 to 8,114 in 2011. The top 10 leading causes of death accounted for 52% of all deaths registered in 2011, and the top 20 leading causes accounted for 67.2%. 2.1 LEADING CAUSES OF DEATH (a) , Australia - Selected years - 2002, 2006, 2011 (b) 2002 2006 2011 Cause of death and ICD code no. Rank no. Rank no. Rank Ischaemic heart diseases (I20-I25) 26 063 1 23 132 1 21 513 1 Cerebrovascular diseases (I60-I69) 12 533 2 11 479 2 11 251 2 Dementia and Alzheimer disease (F01, F03, G30) 4 364 6 6 550 4 9 864 3 Trachea, bronchus and lung cancer (C33-C34) 7 303 3 7 353 3 8 114 4 Chronic lower respiratory diseases (J40-J47) 6 256 4 5 463 5 6 570 5 Diabetes (E10-E14) 3 329 9 3 669 8 4 209 6 Colon, sigmoid, rectum and anus cancer (C18-C21) 4 649 5 3 857 6 4 087 7 Blood and lymph cancer (including leukaemia) (C81-C96) 3 791 7 3 700 7 3 978 8 Heart failure (I50-I51) 3 367 8 2 902 11 3 488 9 Diseases of the urinary system (N00-N39) 2 887 11 3 197 9 3 386 10 Prostate cancer (C61) 2 852 12 2 951 10 3 294 11 Breast cancer (C50) 2 716 13 2 643 13 2 937 12 Influenza and pneumonia (J09-J18) 3 084 10 2 711 12 2 492 13 Pancreatic cancer (C25) 1 834 15 2 077 15 2 416 14 Intentional self-harm (X60-X84)(c) 2 320 14 2 118 14 2 272 15 Skin cancers (C43-C44) 1 462 17 1 648 17 2 087 16 Accidental falls (W00-W19) 629 38 1 288 20 1 845 17 Hypertensive diseases (I10-I15) 1 353 20 1 500 18 1 802 18 Cardiac arrhythmias (I47-I49) 1 226 21 1 280 21 1 612 19 Cirrhosis and other diseases of liver (K70-K77) 1 354 19 1 416 19 1 589 20 (a) Causes listed are the leading causes of death for all deaths registered in 2011, based on WHO recommended tabulation of leading causes. See Explanatory Notes 41-43 for further information. (b) See Explanatory Notes 81-99 for further information on specific issues relating to 2011 data. (c) Excludes Sequelae of suicide (Y87.0) as per the WHO recommended tabulation of leading causes. Care needs to be taken in interpreting figures relating to suicide. See Explanatory Notes 92-95. Previous Page Next Page

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Breast Cancer is New Zealand’s 3rd most common cancer and in the US, almost 40,000 women died from breast cancer last year. Women are encouraged to self examine their breasts so that they become aware of any changes or lumps which may appear at which point they are advised to visit a medical professional where a clinical breast exam (CBE) will be carried out. This involves a doctor or a nurse using their hands to examine the patients breasts using their fingers to try and feel any lumps or bumps under the skin. If something is found, then the next step is to refer the patient to a mammogram or to have a biopsy. The big issue is that due to the poor sensitivity of the human hand, clinical breast exams typically don’t find a lump until they are 21mm in length, yet early detection is crucial as if a cancerous lump is found in the breast when it is only 10mm it improves a patient’s survival rate by more than 94% compared to patients that do not have early detection of tumours. In my Radio Live interview last week I discussed a new nanotechnology film that is being dubbed “electronic skin” which could help to create an image of objects that lie underneath breast tissue. Imagine a thin strip of plastic being placed over your breast and the doctor carrying out the breast examination over the strip creating a savable image of any lumps within your breast. A different doctor could then carry out the same test over a film a few months later and could compare it to the previous results. This type of reporting has not been possible using standard breast examinations because the results are qualitative and very much based on what the doctor feels and records which could vary by their experience level and touch sensitivity. Created by Chieu Van Nguyen and Professor Ravi Saraf from the University of Nebraska-Lincoln, this thin film was created and put to the test by placing lumps of objects inside a piece of silicone to simulate a tumour within the breast tissue. In lab tests, using the same amount of pressure that a doctor would use in a clinical breast exam, the thin film device was able to successfully identify lumps down to 5mm in diameter and up to 20mm in depth which far exceeded what human touch would be able to detect. The 150nm film was able to image subsurface objects in silicone identifying their shape and size. Image adapted from original paper Their research published in the journal American Chemical Society Applied Materials & Interfaces describes how their 150nm ‘skin’ is filled with alternating sandwich layers of gold and cadmium sulfide nanoparticles. These nanolayers have a constant bias of 18 volts across them and when the surface of the film was touched, the pressure from the finger touching them converted the local pushing force into a buckling within the film layers diverting the current. This film was connected to an electro-optical device which measured the change in current from the buckling and converted it to an optical signal where the variation in light emission created an image on a camera (as shown in the blue image on the right). So as amazing as this technology is, it’s still in the research stage. Ravi Saraf estimates that a prototype device could be made within a year at the cost of about $1.5 million however no reports have been made regarding and securing of funding for commercialisation yet. Sciblogs Archive Sciblogs is the biggest blog network of scientists in New Zealand, an online forum for discussion of everything from clinical health to climate change. Our Scibloggers are either practising scientists or have been writing on science-related issues for some time. They welcome your feedback! Sciblogs was created by the Science Media Centre and is independently funded

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Introduction ============ The discovery of microsatellites, and other hypervariable genetic markers, has enabled the study of genetic differentiation and population subdivision at small scales (e.g. [@b57]), even down to the level of the individual (e.g. [@b7]; [@b51]; [@b52]). The information gathered can have important implications for conservation work intended to preserve genetic variation. The significance of this objective increased following the World Summit on Sustainable Development and the publication of the framework for action on biodiversity and ecosystem management, which identifies genetic variation as one of the three levels of biodiversity recommended for conservation ([@b76]). Information on the scale over which genetic differentiation occurs also has important implications for the management of natural resources and the potential for local adaptation. Studies into freshwater salmonid fishes have revealed that genetic differentiation can occur over very short distances within river catchments. This can be associated with physical barriers to movement, which can isolate populations that then differentiate by genetic drift ([@b33]). In addition, differentiation has also been noted where salmonids exist without such barriers, including populations of the many anadromous species that could potentially be linked by gene flow ([@b69]; [@b65]; [@b2]; [@b55]). As such, these species represent an interesting case for studying processes of population differentiation. Specifically, the propensity towards population subdivision appears linked to two key factors: (a) the well-known ability of salmonids to home back to specific natal rivers ([@b68]) and (b) the patchy distribution of spawning areas within rivers ([@b44]) that may act to restrict gene flow among fish in different areas of a river (although other processes e.g. extinction-recolonization dynamics have also been described; [@b47]). Amongst salmonid species, the brown trout (*Salmo trutta*) is typified by having a particularly complex within catchment genetic structure, with high levels of genetic differentiation and an apparent lack of correlation between genetic and geographic distance ([@b4]; [@b12]; [@b22]; [@b43]; [@b61]; [@b62]; but also see [@b8]; [@b19]). Recently there has been an increasing emphasis placed on understanding the deeper biological significance of this complex population structure and there is a need to understand the underlying evolutionary models that may explain the observed patterns of genetic differentiation, which also have important implications for the ecology of brown trout, as well as the conservation of genetic diversity and management of the species. However, brown trout are under pressure from habitat destruction, pollution, over-exploitation and stocking with non-native fish, i.e. local factors that may erode the high levels of genetic variation observed and cause the extinction of unique varieties and loss of unique traits ([@b22]). Although the River Dart is no exception to the pressures that threaten the persistence of brown trout at a local scale, it does drain a National Park and so benefits from a relatively high level of statutory protection. Regular electrofishing surveys undertaken by the Environment Agency (EA; the national regulatory body in England and Wales) suggest that numbers of brown trout within the River Dart are significant and stable, although there has been a negative trend since records began in the 1960s ([@b70]; [@b14]). Changes in land use have led to habitat degradation in the headwaters, although a major threat facing trout in the River Dart arises from both human mediated and natural acidification. The low pH values which characterize the River Dart, combined with the fact that brown trout may spawn in small rivers ([@b17]), may make Dart trout more susceptible to catastrophic events. In turn, this may lead to localized extinctions and recolonizations, with important implications for patterns of genetic differentiation among groups of brown trout ([@b28]; [@b47]). Alternatively, the naturally low pH of rivers on Dartmoor may actually have promoted the tolerance of high acidity in indigenous populations of trout, generating the potential for local adaptation ([@b72]). The purpose of this study was to investigate the population genetic structure of brown trout at the scale of a single river catchment and to reconcile the potential for environmental instability to cause localized extinction events (e.g. [@b47]; [@b37]; [@b44]) with the apparently stable trout numbers present in the River Dart. [@b24] have previously proposed three scenarios that form an appropriate framework for addressing this question. Under the member-vagrant model, nursery areas play a vital role in determining population structure and selection favours individuals that return to their natal spawning grounds to reproduce, which maximizes survival of the young and promotes the development of locally adapted gene pools. Thus, fish that complete this process of homing are considered 'members', contributing to local adaptation and those that do not return to natal areas are known as 'vagrants' ([@b34]; [@b24]). This model predicts temporal stability of population structure, a significant effect of isolation-by-distance and strong genetic differentiation among populations. Under the second model, the metapopulation model, the degree of genetic structuring depends on the temporal stability of habitats, so in an unstable environment the occurrence of locally adapted gene pools can be curtailed because of local extinctions (and subsequent recolonizations, reviewed in [@b3]; [@b41]; [@b59]). The key features of this model are that local populations (or subpopulations) are interconnected not only by migration but also recolonization and empty/unoccupied patches have an important role in metapopulaton dynamics. This model predicts that there would be lower levels of temporal stability in population structure, no significant effect of isolation-by-distance and lower genetic divergence between subpopulations (but still statistically significant because of founder effects, [@b24]; [@b41]; [@b59]). The third scenario is panmixia, where gene flow is unrestricted across the catchment and suggests the absence of genetic differentiation, such that neither of the previous two models applies. Elucidation of the evolutionary model appropriate to Dart trout offers the potential not only to aid local management and conservation, but also to begin to address the relative scarcity of population genetics research completed on salmonids in England and Wales. The present study examined the variability at nine microsatellite loci in brown trout sampled from the River Dart over a 3-year period, with the specific aim of ascertaining the pattern of genetic differentiation within a river system that is particularly vulnerable to severe pH depressions. The results from this analysis, which included application of the decomposed pairwise regression (DPR) method that allowed the relative strengths of genetic drift and gene flow to be accessed in each sample, were then used to consider which evolutionary model (member-vagrant, metapopulation or panmixia) best fitted the data. In addition, spatial autocorrelation was also employed to determine the geographic scale over which genetic differentiation occurred in Dart trout: the conservation implications of these results are discussed. Methods ======= The study area -------------- The River Dart catchment is located in Devon, southwest England ([Fig. 1](#fig01){ref-type="fig"}). It is approximately 75 km long, covers an area of 475 km^2^ and flows into the English Channel through the Dart Estuary and into Start Bay. The river rises on Dartmoor National Park, an upland granite mass that reaches over 600 m high. The catchment is a typical moorland system, characterized by high rainfall and a peaty, acidic soil. The area represents the largest unglaciated expanse of upland in Great Britain and the largest granite surface in England. There are no real aquifers on Dartmoor and water is primarily stored in wetlands and bogs. The river is formed from two main tributaries, the East and West Dart. The upper reaches support small-scale livestock farming, which becomes more intensive and incorporates arable farming once it flows off the moor. ![Map of the River Dart. Grey dots indicate sampling sites, which are accompanied by abbreviated sample names that match those in [Table 1](#tbl1){ref-type="table"}. Significant barriers to fish movement are indicated by double lines perpendicular to the river.](eva0002-0537-f1){#fig01} The catchment supports a locally important stock of resident and anadromous trout (see rod-catch data below), with all the tributaries and several stretches of the main river containing excellent spawning and nursery areas. In particular, many of the headwaters provide valuable spawning grounds, not only for brown trout, but also Atlantic salmon (*Salmo salar* L.). The river also supports a rod/game fishery, as well as a limited commercial estuary (seine) net fishery. Catches of sea trout in 2002, the year this study began, were 712 for rod catches and 727 for net catches ([@b15]). Formal records of brown trout stocking in the UK were first collected by the national river boards during the 1950s and show that in the period up to 2005, 145 212 individual ova, fry or smolt were stocked into the River Dart. These comprised 65 separate stocking events at a minimum of 18 discrete locations within the river. The largest single stocking incident was of 96 000 eyed ova into the headwaters of the East Dart in 1961 (this single event accounts for the majority of all recorded stocking on the River Dart). The source of most stocked trout is thought to be various local hatcheries from southwest England, but the ultimate origin of hatchery stocks has been impossible to uncover ([@b23]). In the last decade local fisheries groups have taken to stocking the lower reaches of the River Dart with much smaller numbers (in the hundreds) of hatchery reared smolt which are typically bred from trout of Dart origin. Sample collection ----------------- A total of l1225 brown trout of multiple year classes, but predominantly parr and excluding fry (to avoid collecting siblings; [@b30]), were collected by electrofishing from 22 sites spread across 14 tributaries within the River Dart catchment. Five of these sites were isolated above barriers; the Gata and the Ash above man-made weirs and the Rud group of samples above a natural waterfall ([Fig. 1](#fig01){ref-type="fig"}). The average in-water distance among sample sites was 22.7 km, with a range of 0.8--64.4 km. Sampling was carried out each summer (July--September), from 2002 to 2004 ([Table 1](#tbl1){ref-type="table"}; [Fig. 1](#fig01){ref-type="fig"}). The adipose fin was removed from each fish and preserved in 98% ethanol, after which the fish was released; removal of the adipose fin provided a permanent mark so the same individuals were not sampled again in subsequent years. ###### Sample site abbreviations Abbreviation Latitude Longitude Details Year *n* -------------- ------------ ----------- ---------------------------------- ------ ----- Amm 50°28′27″N 3°39:44″W Amm Brook, Amm house weir 2002 32 Ash 50°31′50″N 3°45′26″W Ashburn, Belford Hill 2002 36 Dury 50°35′06″N 3°53′26″W Dury Brook, Dury Farm 2002 33 EDar 50°35′44″N 3°54′49″W East Dart, Postbridge 2002 21 EWebB 50°35′21″N 3°48′27″W East Webburn, Bagpark Estate 2003 28 EWebD 50°34′12″N 3°48′40″W East Webburn, Dunstone Bridge 2004 57 EWebV 50°34′32″N 3°48′25″W East Webburn, Veton Bridge 2003 49 EWebW 50°35′08″N 3°48′26″W East Webburn, Wooder Manor 2002 25 EWebW 50°35′08″N 3°48′26″W East Webburn, Wooder Manor 2003 52 Gata 50°27′08″N 3°37′49″W Gatacombe River 2002 34 Har 50°25′55″N 3°46′54″W Harbourne, Hatcheries Fish Farm 2002 41 Hem 50°27′45″N 3°40′08″W River Hems 2002 40 Hol 50°30′15″N 3°49′47″W Holly Brook 2002 29 LChe 50°33′27″N 3°55′55″W Cherry Brook, Lower Bridge 2002 32 LChe 50°33′27″N 3°55′55″W Cherry Brook, Lower Bridge 2003 27 RudB 50°32′55″N 3°47′46″W Ruddycleave, Bowden Farm 2003 42 RudB 50°32′55″N 3°47′46″W Ruddycleave, Bowden Farm 2004 54 RudC 50°32′39″N 3°48′05″W Ruddycleave, Ruddycleave Cottage 2003 36 RudP 50°33′28″N 3°47′11″W Ruddycleave, Pudsham Down 2002 21 RudP 50°33′28″N 3°47′11″W Ruddycleave, Pudsham Down 2003 38 RudP 50°33′28″N 3°47′11″W Ruddycleave, Pudsham Down 2004 39 Swin 50°32′33″N 3°54′36″W River Swincombe, Wydemeet 2002 32 Swin 50°32′33″N 3°54′36″W River Swincombe, Wydemeet 2004 48 UChe 50°34′38″N 3°55′58″W Cherry Brook, Upper Bridge 2003 29 UChe 50°34′38″N 3°55′58″W Cherry Brook, Upper Bridge 2004 41 WDar 50°33′47″N 3°57′53″W West Dart, Cockern Tor 2002 39 WDar 50°33′47″N 3°57′53″W West Dart, Cockern Tor 2003 32 WDar 50°33′47″N 3°57′53″W West Dart, Cockern Tor 2004 48 Web 50°31′35″N 3°47′43″W River Webburn, Mistresses Piece 2002 32 WWeb 50°33′03″N 3°50′03″W West Webburn, Pondsworthy Bridge 2002 47 WWeb 50°33′03″N 3°50′03″W West Webburn, Pondsworthy Bridge 2003 32 WWeb 50°33′03″N 3°50′03″W West Webburn, Pondsworthy Bridge 2004 46 WWebL 50°34′26″N 3°51′02″W West Webburn, Lower Cator Bridge 2002 33 Location details, year of sample collection and numbers of fish sampled (*n*). See [Fig. 1](#fig01){ref-type="fig"} for locations. Microsatellites --------------- DNA was extracted from the fin tissue according to an ammonium acetate precipitation method, similar to that described in [@b5]. Genetic variation was determined at nine di-nucleotide microsatellite loci: Str15, Str60, Str73 ([@b18]), Str85 ([@b54]), SsoSL417, SsoSL25 ([@b64]), Strutta58 ([@b53]), SsoSL438 (A. Slettan, unpublished data, GenBank accession no. Z49134) and SsHaeIII.14.20 (J. L. Goodier unpublished, GenBank accession no. U10050). Genotypes were assayed through polymerase chain reaction (PCR) and polyacrylamide gel electrophoresis with fluorescently labelled primers. PCR reactions were carried out in 10 μL reaction volumes and standard PCR reagents were used in a mixture containing 10--100 ng DNA, 0.5 μ[m]{.smallcaps} of each primer, 1--1.5 m[m]{.smallcaps} MgCl~2~, 200 μ[m]{.smallcaps} of each dNTP, 1× reaction buffer and 0.5 U of *Taq* DNA polymerase (Bioline, London, UK). The PCR profile consisted of: a single denaturing set lasting 3 min at 94°C, 30 iterations of 94°C for 30 s, annealing temperatures 51°C (Str85), 52°C (Str15 & Sso417), 54°C (Sso25 & Strutta58), 58°C (SsHae), 60°C (Str 73) or 65°C (Str60) for 30 s and 72°C for 30 s with a single elongation step of 72°C for 10 min. However, the Sso438PCR profile was a stepwise program, with the annealing stage made up of six iterations at 1° intervals between 54°C and 48°C. For those loci producing weak products (SsHae, Str15 and Str73) 40 iterations were generally used. Size determination of the labelled PCR products was performed using a Beckman-Coulter (Fullerton, California, USA) CEQ8000 automated DNA sequencer with an internal size standard, according to the manufacturer\'s instructions. The raw data were analysed with the platform\'s-associated fragment analysis software (Beckman-Coulter). Genetic diversity analysis -------------------------- ARLEQUIN version 3 ([@b63]) was used to estimate the variance components in allele frequencies among years ([@b20]) and all samples were found to exhibit temporal stability (see Results). Therefore, in subsequent analyses temporal samples from a location were combined to estimate population allele frequencies, as recommended by [@b75]. Each sample at each locus was tested for conformity to Hardy--Weinberg equilibrium (HWE; [@b26]) using GENEPOP 3.4 ([@b56]) and any deviations were further investigated with Microchecker ([@b46]). Critical levels of significance for simultaneous tests were adjusted using the sequential Bonferroni procedure for multiple tests ([@b58]). In addition, Powermarker version 3.25 ([@b40]) was used to calculate expected and observed heterozygosity, and FSTAT version 2.9 ([@b25]) was used to calculate allelic richness (allele number corrected for sample size using the rarefaction method of [@b16]) and the inbreeding coefficient. To examine the levels of genetic differentiation between pairs of samples a test of the homogeneity of allele frequency distributions (the so-called test of 'genic differentiation') was run in GENPOP ([@b56]) and *F*~ST~ values were calculated ([@b77]) in ARLEQUIN. Critical levels of significance for simultaneous tests were adjusted using the sequential Bonferroni procedure for multiple tests ([@b58]). The chord distance (*D*~CE,~[@b10]) was also used to quantify genetic differentiation between samples. This measure was chosen because the close proximity of samples included in the study means mutation is unlikely to have contributed to population divergence and the *D*~CE~ distance is based on geometric distances, which are independent of models of microsatellite mutation ([@b40]). It has also been shown to be one of the most efficient methods for obtaining correct tree topology using microsatellite data ([@b71]). Neighbour-joining (NJ) phylograms were constructed and confidence intervals on tree topology were estimated by bootstrap resampling of loci 1000 times utilizing the programs P[owermarker]{.smallcaps} version 3.23 ([@b40]), C[onsense]{.smallcaps} (from Phylip 3.6; [@b21]) and T[ree]{.smallcaps} V[iew]{.smallcaps} version 1.6 ([@b48]). Decomposed pairwise regression analysis --------------------------------------- To detect outlier populations and accurately elucidate patterns of isolation-by-distance, the DPR ([@b37]) was applied. The DPR can also estimate the relative strengths of genetic drift and gene flow for each sample, by decomposing the regression of the pairwise genetic and geographic distances ([@b60]). Briefly, genetic distance \[*F*~ST~/(1 − *F*~ST~)\] is plotted against geographic distance for all pairwise comparisons. Outlier analysis then determines which samples have exceptional characteristics that may falsely influence the pattern of IBD (e.g. founder effects, bottlenecks, physical barriers, all of which can strongly affect the overall pattern). These outlying samples were determined based on the systematic bias of the regression residuals (process one, which identifies 'putative' outliers). The outliers were then sequentially removed from the analysis and the best model was selected based on the AIC (Akaike\'s information criteria) value (process two, which identifies 'true' outliers); the smallest values indicate the most plausible model ([@b6]). Because of the small sample sizes, the corrected AIC (AIC~C~) was used. Finally, after determining the best model and the 'true' outliers, the pairwise genetic and geographic distances were regressed separately for each sample (including the outlier samples) against the nonoutlier samples, to investigate the different patterns of geneflow and drift. The significance of the relationship was assessed by ordinary least-squares regression. Spatial autocorrelation analysis -------------------------------- Spatial genetic structure was tested with the software package [genalex]{.smallcaps} version 6.1 ([@b50] and according to [@b55]). A Mantel test of matrix correspondence was used to examine the association between pairwise *F*~ST~ values and the in-water distance between sampling sites by estimating the *r*~*xy*~ measure that is analogous to an autocorrelation coefficient ([@b67]), with 999 permutations used to test the statistical significance of the values. At the scale of individual specimens, a multivariate microspatial autocorrelation approach was also employed ([@b66]; [@b51]). This test employed the squared distances measure (PhiPT; [@b51]) to estimate individual genetic distance, and the same in-water distances between sample sites used in the Mantel test for distance between individual specimens (with the exception that all individuals caught from the same sample site were assigned a distance value of zero). To assess the extent of nonrandom genetic structure among individuals ([@b51]), a correlogram of the autocorrelation coefficient (*r*) was plotted as a function of distance, specifically five distance classes: 0--5, 6--15, 16--25, 26--45, 46--65 km; a range of alternate distance classes from 5 to 25 km were also analysed. A multi-distance class (MDC) analysis was also used to give a more accurate estimate of the scale over which genetic structure was detected ([@b51]). In this approach the same classes as above were utilized, except that multiple analyses were performed with automatically increasing distance size classes, such that individuals from more distant classes were added to the previous groups ([@b51]). One thousand bootstrap replicates were used to ascertain the 95% confidence interval (CI) of the *r* estimates, and 999 permutations were used to resolve the 95% CI about the null hypothesis of no spatial genetic structure. Significant genetic autocorrelation was concluded when the CI of *r* and those of the null hypothesis did not overlap ([@b51]). Results ======= Genetic diversity ----------------- Pairwise testing of temporal samples revealed only one case of significant genetic heterogeneity between 2003 and 2004 samples at the RudB site in locus Strutta58 (*P* \< 0.05, corrected across loci; *k* = 9). Furthermore, quantitative estimates of hierarchical gene diversity across the whole dataset showed that while a significant amount of genetic variation (*P* \< 0.00001) was identified both within samples and among different sample sites (96% within samples and 4% between sites), a nonsignificant estimate of 0% variation was attributed to variation among temporal samples. Therefore, all temporal samples collected at individual sites were pooled in subsequent analyses. Genetic diversity indices for each locus and population are presented in [Table 2](#tbl2){ref-type="table"}. Significant deviations from HWE (*P* \< 0.05, corrected across loci; *k* = 9) for pooled samples were detected in two cases (EDar at SsoSL25 and EWebW at Str73). Further analysis of these cases with Microchecker did not reveal any evidence of null alleles or scoring errors, although the EDar case was associated with a significantly positive *F*~is~ value ([Table 2](#tbl2){ref-type="table"}), which could result from the nonrepresentative sampling of juveniles fish ('family sampling'; [@b1]; [@b30]; [@b78]). The mean number of alleles at a locus, across the whole dataset was 10.7 and ranged from 3 (Str60) to 27 (Str58). The mean number of alleles per locus within samples had an average of 6.6 and ranged from 4.4 (RudB) to 8.0 (Har). The allelic richness (the average allele number within samples, corrected for a minimum sample size of 16 in this case) was smaller, with an average of 5.5 and ranged between 4.0 (RudB) and 6.6 (Har). The average observed heterozygosity (H~O~) across all samples was 0.6 and varied from 0.55 (RudP) to 0.74 (Amm). ###### Microsatellite diversity indices of the samples collected from 22 sites and results of the Hardy--Weinberg equilibrium test Sample Indices SsHae Str15 Str58 Str60 Sso25 Sso438 Str73 Sso417 Str85 Mean -------- --------- -------- -------- ----------- -------- ----------- ----------- ---------- -------- -------- -------- Amm *N* 32 32 32 32 32 27 32 32 31 *A* 10 5 13 2 10 4 4 8 6 6.889 A~R~ 8.616 4.488 10.919 2 8.32 3.83 3.5 7.632 5.389 6.077 H~E~ 0.843 0.695 0.88 0.482 0.812 0.582 0.604 0.829 0.64 0.708 H~O~ 0.875 0.844 0.969 0.438 0.844 0.593 0.625 0.813 0.677 0.742 *F*~is~ 0.294 −0.198 −0.085 0.109 −0.024 0.001 −0.018 0.036 −0.041 −0.032 HWE −0.22 0.142 0.112 0.744 0.567 0.761 0.61 0.161 0.96 Ash *N* 36 33 35 36 36 36 34 35 36 *A* 9 5 11 2 8 3 5 9 5 5.889 A~R~ 7.51 4.223 8.22 2 6.494 2.606 4.955 6.997 4.138 5.238 H~E~ 0.824 0.671 0.644 0.277 0.766 0.155 0.74 0.782 0.639 0.611 H~O~ 0.916 0.667 0.657 0.277 0.805 0.111 0.823 0.828 0.722 0.645 *F*~is~ −0.098 0.022 −0.006 0.014 −0.037 0.3 −0.099 −0.045 −0.116 −0.042 HWE 0.453 0.986 0.708 1 0.858 0.858 0.094 0.363 0.374 Dury *N* 33 33 33 33 33 33 33 33 32 *A* 7 5 10 2 8 4 3 9 5 6.222 A~R~ 5.931 4.608 8.451 2 6.828 3.738 3 6.925 4.827 5.145 H~E~ 0.74 0.695 0.817 0.5 00 0.733 0.639 0.633 0.777 0.535 0.674 H~O~ 0.909 0.757 0.787 0.575 0.727 0.696 0.636 0.727 0.593 0.712 *F*~is~ −0.214 −0.075 0.052 −0.136 0.024 −0.074 0.01 0.08 −0.094 −0.041 HWE 0.31 0.459 0.454 0.489 0.121 0.058 0.987 0.093 0.361 EDar *N* 21 21 20 21 21 21 16 21 21 *A* 6 6 11 2 8 4 3 8 6 6 A~R~ 5.699 5.522 9.963 2 7.233 3.946 3 7.471 5.472 5.59 H~E~ 0.732 0.68 0.837 0.495 0.783 0.620 0.646 0.781 0.594 0.685 H~O~ 0.619 0.666 0.85 0.619 0.619 0.571 0.437 0.857 0.666 0.656 *F*~is~ 0.179 0.044 0.011 −0.226 **0.233** 0.103 0.352 −0.073 −0.098 −0.098 HWE 0.144 0.822 0.549 0.384 0.002 0.279 0.065 0.945 0.904 EWebB *N* 25 26 27 28 28 28 27 28 28 *A* 7 5 13 2 8 4 4 5 6 6 A~R~ 6.142 4.942 10.906 2 6.994 3.809 3.592 4.792 5.103 5.364 H~E~ 0.712 0.686 0.872 0.492 0.686 0.447 0.59 0.689 0.582 0.639 H~O~ 0.72 0.692 0.851 0.571 0.821 0.5 0.629 0.821 0.607 0.69 *F*~is~ 0.03 0.031 0.061 −0.125 −0.161 −0.082 −0.028 −0.156 −0.005 −0.041 HWE 0.969 0.516 0.265 0.705 0.845 0.332 0.965 0.763 0.632 EWebD *N* 53 56 57 57 57 52 56 57 52 *A* 8 5 16 2 9 4 5 10 5 7.111 A~R~ 6.618 4.805 11.322 2 6.829 3.957 3.569 8.182 4.259 5.727 H~E~ 0.769 0.687 0.862 0.49 0.683 0.526 0.605 0.805 0.617 0.671 H~O~ 0.811 0.642 0.877 0.508 0.701 0.634 0.535 0.754 0.634 0.677 *F*~is~ −0.036 0.083 0 −0.02 −0.008 −0.187 0.132 0.081 −0.007 0.009 HWE 0.553 0.28 0.1 1 0.769 0.51 0.336 0.237 0.078 EWebV *N* 48 48 49 48 49 48 48 49 47 *A* 8 5 17 2 9 4 4 11 6 7.333 A~R~ 7.165 4.795 12.381 2 6.752 3.838 3.333 8.405 5.521 6.021 H~E~ 0.809 0.722 0.875 0.477 0.691 0.457 0.603 0.8 0.612 0.672 H~O~ 0.75 0.75 0.918 0.479 0.653 0.458 0.667 0.877 0.489 0.671 *F*~is~ 0.095 −0.017 −0.028 0.017 0.076 0.02 −0.084 −0.075 0.222 0.023 HWE 0.079 0.476 0.858 1 0.485 0.677 0.209 0.651 0.045 EWebW *N* 77 77 77 77 77 77 77 77 77 *A* 7 5 17 2 9 5 4 11 6 7.333 A~R~ 6.245 4.34 11.712 2 6.496 3.608 3.738 8.059 4.227 5.603 H~E~ 0.749 0.688 0.882 0.494 0.668 0.455 0.628 0.77 0.414 0.639 H~O~ 0.853 0.727 0.868 0.467 0.71 0.447 0.608 0.84 0.446 0.663 *F*~is~ −0.125 −0.044 0.029 0.067 −0.05 0.031 0.046 −0.076 −0.06 −0.024 HWE 0.337 0.649 0.115 0.648 0.097 0.27 0.001 0.13 0.142 Gata *N* 34 34 34 34 34 32 32 34 34 *A* 6 4 7 2 7 3 3 5 4 4.556 A~R~ 5.925 3.991 6.185 2 6.579 2.5 3 3.94 2.941 4.118 H~E~ 0.803 0.711 0.805 0.389 0.82 0.494 0.642 0.638 0.517 0.647 H~O~ 0.823 0.764 0.823 0.411 0.764 0.468 0.656 0.647 0.47 0.647 *F*~is~ −0.01 −0.059 −0.008 −0.043 0.083 0.068 −0.006 0.001 0.106 0.014 HWE 0.036 0.76 0.182 1 0.994 0.572 0.485 0.372 0.866 Har *N* 35 39 39 40 41 39 26 38 37 *A* 9 6 19 2 11 4 4 10 7 8 A~R~ 7.81 5.649 13.924 2 7.815 3.635 3.615 8.712 6.364 6.614 H~E~ 0.843 0.798 0.912 0.488 0.775 0.487 0.633 0.845 0.812 0.733 H~O~ 0.8 0.794 0.82 0.45 0.658 0.41 0.615 0.868 0.891 0.701 *F*~is~ 0.066 0.018 0.114 0.092 0.162 0.171 0.049 −0.014 −0.084 0.057 HWE 0.353 0.552 0.145 0.752 0.351 0.294 0.783 0.394 0.888 Hem *N* 40 39 31 40 40 40 40 40 40 *A* 9 5 18 2 11 4 4 9 7 7.667 A~R~ 7.466 4.655 14.027 2 9.235 3.858 3.877 8.033 5.785 6.548 H~E~ 0.824 0.751 0.907 0.474 0.858 0.556 0.674 0.825 0.609 0.72 H~O~ 0.75 0.794 0.935 0.375 0.875 0.575 0.65 0.85 0.6 0.711 *F*~is~ 0.103 −0.045 −0.014 0.222 −0.006 −0.02 0.048 −0.018 0.028 0.025 HWE 0.281 0.831 0.616 0.185 0.735 0.808 0.371 0.845 0.323 Hol *N* 26 29 29 29 29 17 24 25 28 *A* 10 6 13 3 9 4 3 9 6 7 A~R~ 9.109 5.535 10.373 2.552 7.718 3.998 3 8.017 5.806 6.234 H~E~ 0.826 0.775 0.848 0.463 0.717 0.624 0.6 0.752 0.718 0.703 H~O~ 0.807 0.724 0.862 0.482 0.758 0.47 0.541 0.8 0.714 0.684 *F*~is~ 0.043 0.083 0.002 −0.025 −0.04 0.275 0.119 −0.042 0.024 0.046 HWE 0.353 0.309 0.191 1 0.898 0.08 0.308 0.588 0.735 LChe *N* 58 59 57 55 58 58 52 59 57 *A* 8 5 16 2 9 5 4 10 5 7.111 A~R~ 6.95 4.555 10.839 2 6.37 4.155 3.846 8.651 4.677 5.783 H~E~ 0.789 0.625 0.872 0.495 0.745 0.622 0.629 0.851 0.571 0.689 H~O~ 0.741 0.627 0.807 0.472 0.793 0.724 0.73 0.949 0.578 0.713 *F*~is~ 0.078 0.014 **0.093** 0.063 −0.047 −0.147 −0.141 −0.098 0.004 −0.018 HWE 0.403 0.686 0.171 0.787 0.488 0.107 0.719 0.364 0.372 RudB *N* 90 92 94 96 93 92 90 94 92 *A* 5 5 8 2 3 3 4 6 4 4.444 A~R~ 4.508 4.679 7.681 2 2.994 2.744 3.069 5.137 3.615 4.047 H~E~ 0.677 0.704 0.828 0.496 0.554 0.426 0.524 0.687 0.555 0.606 H~O~ 0.722 0.75 0.787 0.479 0.58 0.326 0.422 0.659 0.543 0.585 *F*~is~ −0.055 −0.053 0.061 0.045 −0.037 **0.245** 0.206 0.052 0.033 0.045 HWE 0.334 0.58 0.434 0.686 0.453 0.014 0.021 0.022 0.927 RudC *N* 35 36 36 36 36 36 35 34 36 *A* 6 6 9 2 4 3 4 6 4 4.889 A~R~ 5.332 5.262 7.957 2 3.693 2.953 3.825 5.839 3.953 4.535 H~E~ 0.625 0.576 0.832 0.475 0.569 0.519 0.591 0.781 0.664 0.626 H~O~ 0.628 0.556 0.972 0.583 0.583 0.472 0.685 0.852 0.778 0.679 *F*~is~ 0.025 0.065 −0.14 −0.199 0.003 0.119 −0.131 −0.061 −0.144 −0.056 HWE 0.093 0.172 0.754 0.305 0.11 0.685 0.122 0.578 0.312 RudP *N* 96 94 94 98 95 92 96 96 95 *A* 5 5 10 2 3 3 4 8 4 4.889 A~R~ 4.904 4.67 7.256 2 2.817 2.538 3.852 5.251 3.27 4.062 H~E~ 0.706 0.644 0.802 0.462 0.467 0.428 0.595 0.64 0.246 0.554 H~O~ 0.708 0.595 0.787 0.489 0.505 0.445 0.5 0.645 0.242 0.546 *F*~is~ 0.008 0.086 0.03 −0.049 −0.069 −0.028 **0.17** 0.003 0.027 0.026 HWE 0.745 0.007 0.106 0.669 0.136 0.768 0.109 0.174 0.097 Swin *N* 76 80 80 80 80 74 80 80 74 *A* 9 5 17 2 11 4 5 10 8 7.889 A~R~ 6.327 4.667 11.744 2 7.182 3.858 3.688 9.061 6.225 6.084 H~E~ 0.753 0.707 0.886 0.471 0.786 0.558 0.636 0.849 0.707 0.706 H~O~ 0.802 0.737 0.912 0.425 0.837 0.621 0.7 0.85 0.783 0.741 *F*~is~ −0.052 −0.03 −0.017 0.111 −0.052 −0.099 −0.088 0.012 −0.094 −0.036 HWE 0.292 0.335 0.428 0.352 0.133 0.594 0.217 0.186 0.445 UChe *N* 68 70 69 68 67 66 68 64 67 *A* 7 5 15 2 9 5 4 10 7 7.111 A~R~ 6.01 4.86 11.507 2 7.525 3.921 3.417 8.267 5.35 5.837 H~E~ 0.773 0.684 0.891 0.492 0.796 0.588 0.659 0.814 0.599 0.699 H~O~ 0.735 0.657 0.898 0.441 0.716 0.651 0.691 0.796 0.641 0.692 *F*~is~ 0.064 0.054 0.007 0.118 **0.116** −0.093 −0.033 0.038 −0.056 0.026 HWE 0.765 0.086 0.244 0.462 0.17 0.592 0.735 0.535 0.865 WDar *N* 114 112 116 119 118 103 112 118 117 *A* 8 6 15 2 9 5 5 11 7 7.556 A~R~ 5.884 4.62 11.142 2 6.042 3.426 3.286 8.167 4.754 5.48 H~E~ 0.746 0.695 0.89 0.495 0.755 0.544 0.654 0.829 0.579 0.688 H~O~ 0.78 0.687 0.922 0.512 0.779 0.514 0.687 0.813 0.572 0.696 *F*~is~ −0.036 0.02 −0.027 −0.026 −0.023 0.065 −0.041 0.027 0.021 −0.004 HWE 0.736 0.271 0.939 0.854 0.427 0.703 0.991 0.279 0.099 Web *N* 32 32 32 31 32 21 29 28 31 *A* 10 2 12 2 9 4 4 8 6 6.333 A~R~ 8.276 4.994 9.874 2 7.129 3.751 3.551 7.341 5.009 5.769 H~E~ 0.788 0.758 0.871 0.481 0.68 0.447 0.618 0.785 0.53 0.662 H~O~ 0.75 0.781 0.875 0.483 0.656 0.285 0.758 0.785 0.516 0.654 *F*~is~ 0.064 −0.014 0.011 0.011 0.052 **0.383** −0.21 0.017 0.044 0.029 HWE 0.706 0.493 0.474 1 0.029 0.045 0.417 0.11 0.492 WWeb *N* 122 122 114 125 125 115 120 125 112 *A* 11 5 18 2 9 4 4 10 7 7.778 A~R~ 7.546 4.732 11.109 2 6.298 3.875 3.58 8.011 4.844 5.777 H~E~ 0.775 0.728 0.88 0.497 0.681 0.544 0.632 0.838 0.595 0.686 H~O~ 0.778 0.721 0.877 0.44 0.728 0.547 0.633 0.864 0.642 0.692 *F*~is~ 0.005 0.019 0.013 0.124 −0.06 0.002 0.007 −0.022 −0.07 −0.001 HWE 0.276 0.07 0.742 0.221 0.646 0.709 0.191 0.489 0.668 WWebL *N* 29 24 33 33 33 31 31 31 26 *A* 8 5 15 2 8 4 3 11 5 6.778 A~R~ 6.675 4.968 11.846 2 6.531 3.76 3 9.709 4.546 5.893 H~E~ 0.763 0.749 0.891 0.477 0.64 0.493 0.608 0.868 0.507 0.666 H~O~ 0.827 0.75 0.939 0.545 0.515 0.387 0.741 0.87 0.461 0.671 *F*~is~ −0.067 0.02 −0.039 −0.127 **0.21** 0.231 −0.204 0.014 0.11 0.01 HWE 0.176 0.024 0.337 0.711 0.14 0.155 0.406 0.161 0.176 Mean *N* 1178 1188 1187 1216 1213 1137 1150 1196 1158 *A* 13 7 27 3 13 6 5 13 10 A~R~ 6.666 4.798 10.424 2.025 6.54 3.559 3.513 7.39 4.822 H~E~ 0.795 0.734 0.902 0.499 0.741 0.533 0.676 0.836 0.6 H~O~ 0.775 0.705 0.863 0.473 0.707 0.504 0.628 0.802 0.585 *n*, number of individuals; A, number of alleles; A~R~, allelic richness; H~O~, observed heterozygosity; H~E~, expected heterozygosity; *F*~is~, inbreeding coefficient (values in bold differ significantly from zero at the 5% level, although none remained significant after table-wide Bonferroni correction); HWE, *P*-value of the Hardy--Weinberg equilibrium test. Tests for the homogeneity of allele frequency distributions revealed significant genetic differentiation occurred between the majority of the 231 pairwise comparisons, except in nine cases (upper diagonal, [Table 3](#tbl3){ref-type="table"}), of which approximately half involved samples collected from within the same tributary. Quantification of genetic differentiation with *F*~ST~ values (lower diagonal, [Table 3](#tbl3){ref-type="table"}), demonstrated a range of 0.00--0.16, with a global *F*~ST~ of 0.04. The highest *F*~ST~ occurred between samples above significant barriers to fish movement, whereas the lowest, and nonsignificant *F*~ST~ values, tended to occur between (but not exclusively between) proximate samples from the same or neighbouring tributaries. ###### Tests for genetic differentiation between pairs of samples Amm Ash Dury EDar EWebB EWebD EWebV EWebW Gata Har Hem Hol LChe RudB RudC RudP Swin UChe WDar Web WWeb WWebL ------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- ---------- ---------- ------------ Amm **--** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** NS **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** ***^\*^*** Ash **0.050** **--** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** ***^\*^*** Dury **0.021** **0.091** **--** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** EDar 0.016 **0.068** 0.021 **--** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** EWebB **0.023** **0.085** 0.017 0.023 **--** **^\*^** NS NS **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** NS **^\*^** **^\*^** EWebD **0.025** **0.068** **0.021** 0.016 0.005 **--** NS **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** NS **^\*^** **^\*^** EWebV **0.021** **0.054** **0.020** 0.013 0.007 0.007 **--** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** NS **^\*^** **^\*^** EWebW **0.023** **0.077** 0.012 **0.021** 0.000 0.004 0.004 **--** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** Gata **0.050** **0.067** **0.086** **0.073** **0.087** **0.079** **0.058** **0.076** **--** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** Har **0.013** **0.068** **0.042** **0.040** **0.040** **0.032** **0.028** **0.045** **0.079** **--** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** Hem 0.000 **0.041** **0.021** 0.020 0.020 **0.018** 0.018 **0.017** **0.031** 0.011 **--** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** Hol **0.014** **0.050** **0.028** 0.016 **0.029** **0.019** 0.005 **0.020** **0.053** 0.018 0.007 **--** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** LChe **0.019** **0.077** 0.013 0.007 **0.024** **0.019** **0.020** **0.019** **0.077** **0.043** **0.023** **0.026** **--** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** RudB **0.076** **0.119** **0.056** **0.072** **0.039** **0.045** **0.046** **0.044** **0.140** **0.073** **0.071** **0.067** **0.054** **--** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** RudC **0.068** **0.122** **0.056** **0.061** **0.026** **0.027** **0.045** **0.031** **0.129** **0.067** **0.066** **0.065** **0.048** **0.021** **--** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** RudP **0.092** **0.153** **0.053** **0.095** **0.059** **0.078** **0.064** **0.053** **0.160** **0.112** **0.090** **0.090** **0.071** **0.033** **0.061** **--** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** Swin **0.016** **0.079** 0.015 0.013 **0.024** **0.021** **0.026** **0.029** **0.083** **0.027** **0.018** **0.029** 0.011 **0.060** **0.050** **0.090** **--** **^\*^** **^\*^** **^\*^** **^\*^** **^\*^** UChe **0.016** **0.081** 0.012 0.008 0.020 **0.017** **0.021** **0.019** **0.072** **0.036** 0.013 **0.027** 0.000 **0.050** **0.044** **0.071** 0.006 **--** **^\*^** **^\*^** **^\*^** **^\*^** WDar **0.021** **0.065** **0.024** 0.013 **0.034** **0.031** **0.023** **0.034** **0.075** **0.041** **0.018** **0.026** **0.009** **0.063** **0.076** **0.088** **0.014** **0.011** **--** **^\*^** **^\*^** **^\*^** Web **0.029** **0.091** 0.013 0.023 0.000 0.000 0.008 0.002 **0.086** 0.036 0.017 0.022 **0.020** **0.025** 0.018 **0.050** **0.021** 0.014 **0.030** **--** **^\*^** NS WWeb **0.021** **0.077** 0.013 **0.033** 0.011 **0.012** **0.012** **0.011** **0.081** **0.023** **0.019** **0.024** **0.029** **0.040** **0.039** **0.060** **0.025** **0.025** **0.034** 0.005 **--** NS WWebL **0.021** **0.099** 0.013 **0.026** 0.015 0.009 0.010 0.013 **0.086** 0.027 **0.016** **0.025** **0.024** **0.037** **0.034** **0.063** 0.013 **0.016** **0.025** 0.000 0.000 **--** The upper diagonal shows pairwise *F*~ST~ values; all significant values (*P* \< 0.05) are highlighted in bold. The lower diagonal shows the result of tests for homogeneity of allele frequencies: NS, not significant; ^\*^significant at the 5% level. Table-wide significance levels were applied using the sequential Bonferroni procedure (*k* = 231) for all tests. The NJ *D*~CE~ phylogram ([Fig. 2](#fig02){ref-type="fig"}) reveals several samples that have high bootstrap support and relatively long branch lengths, namely the Rud group of samples and the Gata and Ash; this relates well to their positions above significant barriers to fish movement ([Fig. 1](#fig01){ref-type="fig"}) that may have acted to isolate these samples from the rest of the catchment. Moderate support is also noted on the phylogram among groups of samples from the upper west (Che, WDar, Swin, Dury and EDar), upper east (Web, EWeb and WWeb) and lower (Amm, Har, Hol and Hem) areas of the catchment. In addition, there is some support for proximate groups of samples, especially those collected within the same tributary, e.g. within the West and the East Webburn. A principal component analysis (PCA) was also performed on these data using the default settings in [genalex]{.smallcaps} 6 ([@b50]), the findings of which support the main conclusions of the phylogram; the PCA plot in [Fig. S1](#SD1){ref-type="supplementary-material"}. ![Neighbour-joining phylogram based on pairwise *D*~CE~ distances between samples. Numbers next to branch nodes represent bootstrap support (%) based on 1000 replicates, only values over 50% are shown. Sample abbreviations match [Table 1](#tbl1){ref-type="table"}.](eva0002-0537-f2){#fig02} Decomposed pairwise regression ------------------------------ Genetic distance was positively correlated with geographic distance when comparing all pairwise sample combinations, but the correlation was weak and nonsignificant (*P* = 0.137, *r*^2^ = 0.036; [Fig. 3](#fig03){ref-type="fig"}). Based on the systematic bias of the regression residuals (process one) nine putative outlier samples were detected; RudP, Ash, Gata, RudB, RudC, Hem, Amm, WDar and UChe. The AIC values were compared for models with and without putative outliers (process two) and the best model included 17 samples (indicating RudP, Ash, Gata, RudB and RudC were true outliers; [Table 4](#tbl4){ref-type="table"}). This result is consistent with *a priori* predictions as all these samples originated from sites above significant barriers to fish movement. The exclusion of these samples strengthened the positive correlation between genetic and geographic distance, which also become statistically significant (*P* \< 0.001, *r*^2^ = 0.476; [Fig. 3](#fig03){ref-type="fig"}). Each of the outlier samples was individually regressed with the nonoutlier samples, which indicated that the majority of outlier samples were significantly diverged from adjacent populations but exhibited strong and significant correlations between genetic and geographic distance ([Fig. 4](#fig04){ref-type="fig"}). This suggests that despite of a strong effect of genetic drift acting on the isolated samples (either through small effective population size or founder effects or bottleneck) evidence of gene-flow still remains. The Ash sample was the exception; while significantly divergent from the other samples, it showed no correlation between genetic and geographic distance, suggesting that the effect of genetic drift far outweighs that of gene flow. The decomposed regressions of the 17 nonoutlier samples showed similar regression lines with significant relationships between genetic and geographic distance, except for the Amm, Hol and Swin ([Fig. 4](#fig04){ref-type="fig"}). This suggests that these samples are close to, or at, equilibrium between drift and gene flow. ![Relationship between genetic distance \[*F*~ST~/(1 − *F*~ST~)\] and geographic distance (km) for all 22 samples (open and closed diamonds combined; *r*~*xy*~ = 0.191, *P* = 0.137, *r*^2^ = 0.036, upper line) and excluding the five outlier samples (filled diamonds only; *r*~*xy*~ = 0.690, *P* \< 0.001, *r*^2^ = 0.476, lower line).](eva0002-0537-f3){#fig03} ###### Fit of alternative models with and without the putative outlier samples Samples excluded *n* *k* *r*^*2*^ *P* value AIC~C~ ΔAIC~C~ --------------------------------------------------- ----- ----- ---------- ----------- --------- --------- RudP, Ash, Gata, RudB, RudC 17 1 0.4768 \<0.001 −108.49 0.00 RudP, Ash, Gata, RudB, RudC, Hem 16 1 0.5281 \<0.001 −103.26 5.23 RudP, Ash, Gata, RudB, RudC, Hem, Amm 15 1 0.6292 \<0.001 −99.37 9.12 RudP, Ash, Gata, RudB, RudC, Hem, Amm, WDar 14 1 0.6504 \<0.001 −94.50 13.98 RudP, Ash, Gata, RudB 18 1 0.1353 0.064 −90.73 17.76 RudP, Ash, Gata, RudB, RudC, Hem, Amm, WDar, UChe 13 1 0.6459 \<0.001 −87.68 20.81 RudP, Ash, Gata 19 1 0.0612 0.1099 −86.11 22.38 RudP, Ash 20 1 0.0880 0.066 −75.52 32.97 RudP 21 1 0.0589 0.076 −72.33 36.16 None 22 1 0.0335 0.142 −68.86 39.63 *n* refers to the number of samples and *k* the number of parameters. ![Decomposed pairwise regression of genetic distance \[*F*~ST~/(1 − *F*~ST~)\] and geographic (km) distances for the 22 samples. Each of the five outlier samples was regressed with the 17 nonoutlier samples, whilst each of the 15 nonoutliers was regressed with the other 14 samples. Solid and dashed lines represent statistically significant or nonsignificant regressions respectively.](eva0002-0537-f4){#fig04} Spatial autocorrelation ----------------------- Tests of microspatial autocorrelation at the level of the individual were carried out on samples not isolated above barriers to fish movement (this included all 17 samples not identified in the DPR as true outliers). The results showed that the genetic autocorrelation coefficient (*r*) was significantly positive at the 0--5 and 5--15 km size classes, and intercepted the *x*-axis at 20 km ([Fig. 5A](#fig05){ref-type="fig"}); results from the analysis of alternative classes produced broadly similar results, with intercepts ranging from 15 to 20 km (results not shown). In all size classes above 15 km, *r* was significantly negative, meaning that proximal individuals showed greater genetic divergence than that expected for a random distribution of genotypes, although in the largest size classes *r* approached the null hypothesis of no significant structure. The MDC analysis with increasing distance size classes revealed that *r* was significantly positive for distance classes up to and including 25 km ([Fig. 5B](#fig05){ref-type="fig"}). The inclusion of specimens separated by \>45 km meant that significant positive genetic autocorrelation was no longer observed. The addition of samples collected above barriers did not radically alter the results of the spatial autocorrelation (analysis not shown), except in the correlogram ([Fig. 5A](#fig05){ref-type="fig"}), in which case *r* was not as strongly negative (*r* = −0.015 in the 25 km class) and at the largest distance class the null hypothesis could not be rejected. However, because of the uncertainties of applying an individual-based test to samples collected at specific sample sites (where separation between individuals is assumed to be zero), these findings should be interpreted with some caution. ![Spatial autocorrelation analyses with samples isolated above barriers removed. (A) correlogram of the genetic correlation (*r*) as a function of distance. (B) The genetic correlation (*r*) as a function of increasing distance classes. Dotted lines (A) and grey bars (B) indicate the 95% confidence interval (CI) about the null hypothesis and error bars about r indicate the 95% CI.](eva0002-0537-f5){#fig05} Discussion ========== The purpose of this study was to examine, within-catchment population structure of brown trout in a region that despite being a focus for salmonid fishing and conservation, has until now, received relatively little attention. The results revealed significant differentiation among samples collected within a single river catchment and, in the case of the Ruddycleave and Cherry Brook, even between sample sites within a tributary. These results demonstrate that Dart trout do not represent a single panmictic population in which gene flow is unrestricted across the catchment. The global *F*~ST~ across all 22 samples sites was 0.04, with a range of 0.000--0.160 for pairwise *F*~ST~ estimates, which accords with previous work on brown trout employing microsatellites (e.g. [@b9], *F*~ST~ = 0.00--0.114; [@b35], 0.009--0.065; [@b31], 0.010--0.071; [@b47], 0.004--0.154). Effect of barriers ------------------ What is particularly striking from the phylogram ([Fig. 2](#fig02){ref-type="fig"}) and pairwise *F*~ST~ estimates ([Table 3](#tbl3){ref-type="table"}) is the effect barriers have on population structure; the largest values all occur between comparisons involving samples isolated above a barrier to fish movement. The significant effect of barriers on population structure has been previously documented and has been associated with reductions in population size, bottlenecks and genetic drift ([@b33]; [@b42]; [@b49]; [@b73]). Such processes may also have been in operation in these isolated samples identified within the River Dart, as the levels of heterozygosity and allelic richness were also depressed ([@b11]). The results of the DPR analysis also afford some further insight into the demographic processes occurring within these samples. In the case of the Ash sample, genetic drift has acted to obscure any correlation between genetic and geographic distance between samples; as the barrier to migration on this tributary is man-made (and therefore not ancient), small effective population size and founder effects appear to be the most likely explanation for the patterns of genetic divergence observed. In the case of the other highly diverged and isolated samples (RudC, RudB, RudP and Gata) a relatively strong correlation between genetic and geographic distance remains, suggesting that effective population sizes have not been reduced to the level that genetic drift is strong enough to obscure the correlation. Alternatively, some form of gene flow could be occurring, perhaps associated with barriers being by-passed in high flows. However, it is interesting to postulate that unidirectional, downstream migration from the isolated areas could act to partially restore the correlation between genetic and geographic distance. The importance of identifying barriers to fish movement has been highlighted for a number of conservation issues, in particular, the negative effects of genetic drift in small populations and the isolation of indigenous stocks from the effects of stocking undertaken below barriers ([@b79]; [@b73]), both topics that appear to warrant further investigation within the River Dart. Population structure and evolutionary models -------------------------------------------- The phylogram ([Fig. 2](#fig02){ref-type="fig"}) shows that genetic structuring among samples within the catchment is present; moderate levels of bootstrap support occurred between three groups of proximate samples from the upper east, upper west and lower Dart. This association between genetic and geographic distance is further supported by a significant effect of isolation-by-distance, as demonstrated by DPR analysis ([Fig. 4](#fig04){ref-type="fig"}). However, a strongly negative genetic correlation (*r*) was identified at the 25 and 45 km size classes used in the spatial autocorrelation on Dart trout ([Fig. 5A](#fig05){ref-type="fig"}), meaning that proximal individuals showed greater genetic divergence than that expected for a random distribution of genotypes. Such a finding may be the result of a discontinuity in gene flow between trout in different tributaries or could reflect the fact that some sampling was completed outside of the spawning season, and therefore, may include adult specimens of trout that may have moved away from nursery areas. The observation of isolation-by-distance at the intra-catchment level is somewhat at odds with many of previous studies describing the population structure of brown trout ([@b12]; [@b22]; [@b43]; [@b4]; [@b61]), although, it is not unique ([@b19]; [@b8]). Recent studies of anadromous brown trout inhabiting relatively small rivers in Denmark and the Baltic Sea ([@b39]; [@b47]; [@b35]) suggested a population structure consisting of a system of highly interconnected, small and unstable populations where, in accordance with the metapopulation model, there was no significant effect of isolation-by-distance and a lack of temporal stability (even over the short-term). This pattern was generally linked to high levels of gene flow and occasional extinction--recolonization events caused by environmental instability, e.g. low summer water levels ([@b47]). These results sharply contrast with the population structure described in this study, where a significant effect of isolation-by-distance (once outliers have been excluded) and at least short-term temporal stability of population structure was observed. Therefore, it appears that, despite the potential for low pH to perturb the environment, the population structure of brown trout inhabiting the tributaries of the River Dart is determined more by ecological events and natal homing, than by rare stochastic extinction events, with migration occurring mostly between neighbouring groups. The key to reconciling these contrasting results among studies appears to be catchment size, whereby larger population systems appear to be stable and smaller systems tend to undergo localized extinction--recolonization events ([@b31]; [@b47]; [@b35]; [@b44]; [@b55]). Historical and temporal effects ------------------------------- There are some limitations to this study; in particular, the effects of postglacial recolonization and stocking on population structure of Dart trout still await assessment. Although, the results of the DPR analysis suggests the majority of the samples are at, or close to, drift--migration equilibrium following such perturbation ([Fig. 4](#fig04){ref-type="fig"}). In particular, these processes (especially artificial stocking), would generally have acted to obscure the strong pattern of isolation-by-distance identified in this study ([@b38]; [@b45]), suggesting they are not the strongest determinants of population structure in this case. In addition, the temporal samples collected in the study represent only a subset of sites from across the catchment and cover a relatively short period: 2002--2004. [@b49] found that the probability of detecting significant allele frequency differences between temporal samples taken from the same population, but spaced only a few years apart, could be small. Indeed, if extinction events happen infrequently, i.e. over the scale of decades, then this instability may not become evident in samples taken only a few years apart (although the strong pattern of isolation-by-distance identified suggests longer term temporal stability, at least as long as it takes for drift--migration equilibrium to be established after perturbation). Evolutionary hypotheses ----------------------- The hypotheses proposed by [@b24] provide a useful framework within which to analyse population structure; however, they remain quite general and any situation in which gene flow is limited by geographic distance may yield similar results. Indeed, work on genetic population structure of Dolly Varden charr (*Salvelinus malma*; [@b37]) yielded analogous results to the present study, but the authors suggested that a source-sink metapopulation structure best fitted their results. In that case, outlier samples were identified in the absence of barriers to migration, suggesting founder effects or bottlenecks had occurred; such factors have not been identified within the current study of the River Dart (where the results of the DPR actually suggest relatively stable population structure). Additionally, many of the predictions of the proposed models are quite simplistic, e.g. the prediction that that there would be no significant pattern of isolation by distance in a metapopulation may not hold true if recolonization and gene flow occurred predominantly between neighbouring populations (a scenario made more likely by the linear nature of a river). Another prediction, that the level of genetic structuring would be expected to be lower under a metapopulation model, can also be questioned. It has been shown that the range of *F*~ST~ estimates in this study is similar to that used previously to describe both small temporally unstable populations ([@b35]) and large stable populations ([@b31]). It appears that levels of differentiation, especially *F*~ST~ values, may not differ under the two evolutionary models summarized by [@b24] and are dependant on the complex mechanics of recolonization ([@b32]; [@b44]). Indeed, extinction--recolonization events may act to increase levels of genetic differentiation ([@b28]; [@b27]). Delineating demographic units ----------------------------- Spatial autocorrelation analyses were used to determine the geographic scale of genetic structuring within the River Dart. [Figure 4B](#fig04){ref-type="fig"} illustrates the tendency for genetic distance between individuals to decrease with increasing distance, such that at in-water distances of \>45 km gene flow is minimal. It has also been proposed that the *x*-axis intercept of the correlogram ([Fig. 5A](#fig05){ref-type="fig"}) be considered as a minimum distance that can conserve genetic diversity at a lower cost ([@b13]), resulting in a management unit size of approximately 15--20 km for the River Dart. The results from spatial autocorrelation analyses bear some similarities to work on Atlantic salmon in the Varzuga River in Russia ([@b55]), which also highlighted the importance of conserving multiple spawning and nursery areas for the long-term preservation of fish populations. However, most striking difference is the distance across which gene flow was observed within the Varzuga; the genetic correlation remained positive at distances up to 120 km and the *x*-axis intercept of the correlogram occurred at 34 km. This may reflect the larger size of the Varzuga River (when compared with the River Dart), and the fact that samples were separated by greater average in-water distances ([@b74]). Alternatively, it is interesting to hypothesize that the lower distance over which gene flow occurs in brown trout may reflect their resident life history, resulting in more restricted gene flow and greater genetic differentiation ([@b29]; [@b36]; [@b44]). Conclusions =========== Brown trout inhabiting the River Dart demonstrate significant within-river population differentiation; this differentiation is most significant when associated with barriers to movement, but otherwise demonstrates a pattern of isolation-by-distance and at least short-term temporal stability. These results are taken as evidence that ecological events are more important in shaping the population structure of Dart trout than stochastic extinction events, and certainly do not contradict the expectations of a member-vagrant evolutionary model of population structure for Dart trout ([@b24]). However, the results of the spatial autocorrelation demonstrate gene flow does occur between neighbouring samples, suggesting the need to conserve not only different spawning areas within the basin (particularly in different tributaries), but links between them as well. This research was supported by funding from the Natural Environment Research Council (NERC), UK through the award of a CASE studentship (NER/S/A/2001/06178) with the Westcountry Rivers Trust (CASE partner) and the award of a NERC training grant to work at the Sheffield Molecular Genetics Facility (SMGF/047). The EA is acknowledged for assistance in sample collection, in particular Fisheries Officers Dave Hoskin and Adam Bailey, without whom the project would not have been possible. Further acknowledgement is also due to all those who helped with fieldwork, especially Jan Shears and Phil Shears, and to Anna Finnegan for provision of stocking data and GIS support. This study also benefited from technical training by members of the Sheffield Molecular Genetics Facility: Terry Burke, Deborah Dawson and Andy Krupa. Supporting Information ====================== Additional Supporting Information may be found in the online version of this article: **Figure S1.** Principal componentanalysis plotted from a matrix of pairwise Nei\'s geneticdistances between all populations and computed using the programgenalex (Peakall andSmouse 2006). Axis 1 explains 36% of the variation and axis 2, 22%of the variation. Populations analysed are the same as thoseanalysed in the phylogram ([Fig. 2](#fig02){ref-type="fig"}); sample abbreviationsmatch [Table 1](#tbl1){ref-type="table"}. Please note: Wiley-Blackwell are not responsible for the content or functionality of any supporting materials supplied by the authors. Any queries (other than missing material) should be directed to the corresponding author for the article.

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Introduction ============ Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous in the environment and cause adverse environmental effects. The exploration and exploitation of crude oil and gas resources are a major source of PAHs. Even though improved technologies have been introduced in the petroleum industry, accidents continue to occur, resulting in hydrocarbon pollution of the environment (both land and water) in most oil producing countries, including Nigeria.[@i2156-9614-9-24-191204-b1] Oil from the petroleum industry enters the aquatic environment through gas flaring, disposal of used lubrication oils, washings from oil tanks, leakage from marine vessels, erosion and run off from crude oil polluted lands, refinery effluents, and ruptures from poorly maintained flow lines/installations. Leakage of oil into the environment could be due to sabotage or maintenance and engineering errors. Upon entry into the aquatic environment, the fraction either mixes with water or sinks into the sediment, causing severe damage to benthic organisms. Hydrocarbon pollution impacts fish, crustaceans and mollusks with objectionable odor or flavor, reducing their market value and acceptability.[@i2156-9614-9-24-191204-b1] Major routes of PAH exposure in fish are ingestion of contaminated food and diffusion of water across their gills and skin.[@i2156-9614-9-24-191204-b2] The lipophilic nature and high chemical stability of PAHs make it easier to penetrate biological membranes and accumulate in the fatty tissues of organisms following their uptake. Polycyclic aromatic hydrocarbons have been reported to be readily absorbed by fish and other aquatic organisms on exposure to contaminated materials, thereby reaching elevated levels over that of the surrounding medium.[@i2156-9614-9-24-191204-b2] The bioaccumulation pattern of PAHs vary in aquatic organisms depending on the trophic levels they occupy, however, the organic PAHs physiological burden is dependent on the biotransformative effect of the organisms.[@i2156-9614-9-24-191204-b3] Macrobenthic invertebrates (shrimps, crayfish, mollusks and crabs) are an important and integral part of the aquatic ecosystem and thus reflect any negative effects caused by pollution in the community structure which can affect trophic relationships.[@i2156-9614-9-24-191204-b4] Fish have been reported to be the most sensitive living organism to trace concentrations of toxicants in aquatic habitats.[@i2156-9614-9-24-191204-b5] Shrimps, crabs and fishes are therefore good indicators of pollution in coastal waters and have been used extensively for environmental monitoring.[@i2156-9614-9-24-191204-b6] Polycyclic aromatic hydrocarbons are classified into two main groups, low and high molecular weights, based on their physical and biological properties and number of fused aromatic rings contained in their structure. Light or low molecular weight (LMW) PAHs consist of 2--3 aromatic rings, and heavy or high molecular weight (HMW) PAHs consist of 4--6 rings.[@i2156-9614-9-24-191204-b7],[@i2156-9614-9-24-191204-b8] The HMW PAHs are more persistent and recalcitrant (less readily bio-degraded by indigenous microorganisms) than LMW PAHs and can persist in an aqueous environment and bioaccumulate in aquatic organisms like fish and shrimps, and are more carcinogenic.[@i2156-9614-9-24-191204-b9] The LMW PAHs, although less carcinogenic, also pose toxic risks to many aquatic organisms.[@i2156-9614-9-24-191204-b10] The stability and distribution of PAHs in the natural environment is influenced by the chemical structure, chemical configuration and physical and chemical properties of the aromatic rings.[@i2156-9614-9-24-191204-b8],[@i2156-9614-9-24-191204-b11] The spectrum of PAHs in the water ecosystem, including water, fish, and sediment can provide some information about their emission source. Higher concentrations of LMW PAHs (e.g., acenaphthene, fluorene) are usually related to naturally occurring PAHs, either of petrogenic or pyrogenic origin, while PAHs emitted from combustion processes (pyrolytic origin) often contain elevated concentrations of HMW (e.g., phenanthrene, fluoranthene, pyrene) and fewer LMW PAHs.[@i2156-9614-9-24-191204-b11] Polycyclic aromatic hydrocarbons have received attention due to their potential negative effects on human and ecosystem health. Adverse effects of PAHs have also been observed in marine organisms, which include impairment in growth and development, growth reduction, endocrine alteration, malformations of embryo and larvae and DNA damage.[@i2156-9614-9-24-191204-b12] *ERL* : Effect range low *ERM* : Effect range median *HMW* : High molecular weight *LMW* : Low molecular weight *SV* : Screening value *TEF* : Toxicity equivalency factor *TEQ* : Toxic equivalent quotient *USEPA* : United States Environmental Protection Agency Aquatic foods are high in nutritive value and thus highly desirable due to their contribution of high-quality protein and low fat content. This attracts consumers to these foods due to their health benefits in addition to their widespread availability and relatively low price, although exposures to toxic chemicals have been a concerning issue for years. In Nigerian markets, fish are one of the most common aquatic organisms available for consumption and reportedly provide over 60% of protein intake.[@i2156-9614-9-24-191204-b15] Food consumption has been identified as an important pathway of human exposure to many contaminants, including PAHs. Therefore, PAH contamination of widely consumed fish species among the populace may have serious health implications as some of these aquatic organisms are caught in water polluted by hydrocarbons.[@i2156-9614-9-24-191204-b16] The objectives of the present study are to determine the concentration of PAHs in sediment samples and in two commercially important fish species, Drepane africana and Pomadasys jubelini, crabs, and shrimps around the Atlas Cove jetty. Additionally, the present study aims to assess the health risk associated with the consumption of fish species and shellfish in the study area. Methods ======= The study was carried out around the Atlas Cove jetty *([Figure 1](#i2156-9614-9-24-191204-f01){ref-type="fig"})*, which is an offloading and storage depot for imported refined oil prior to distribution to other depots. Oil spillage has been reported in the process of operations in Commodore channel. The channel is approximately 10 m deep at the entrance, 12--15 m deep inward, 0.5 - 1 km wide, and 10 km long. It is tidal, and water from the Atlantic Ocean moves in during high tides and recedes during low tides. Turbulence is very high due to its proximity to the Atlantic Ocean. In addition to oil-related activities that go on around the jetty, it is well known for the movement of shipping vessels along the waterways. ![Map of the study area showing sampling points](i2156-9614-9-24-191204-f01){#i2156-9614-9-24-191204-f01} The jetty is located in Lagos State between latitudes 6°21′ N to 6°34′ N and longitudes 3°01′ E to 3°27′ E in the southwestern region of Nigeria. The water around Atlas Cove jetty is brackish (mixture of fresh and marine water). The lagoon plays an important role for the human community due to the large prosperous molluscan and fishing exploitation and commerce. It is also used for artisanal fishing, as a large part of the domestic fish supply in Nigeria comes from inland waters, such as lagoons, and thus provides a means of livelihood for fishermen. However, this industry is being threatened by concentrations of PAHs in this area. Sample collection ----------------- A total of 45 surface sediment samples were collected in five different locations, at 5 cm depth, around Atlas Cove jetty between June to August 2016. Sediment samples were collected from five different sites, all of which were impacted by anthropogenic activities such as ship traffic and offloading. Sediment samples were collected using sediment grab and transferred onto aluminum foil papers. Twelve (12) samples of each fish species and 20 samples of shrimps and crabs were purchased from local fishermen at the landing site of the study area and transported to the laboratory on ice packs. Upon arrival at the laboratory, the samples were removed from the ice, thawed, and cleaned under running tap water to remove any dirt and then rinsed again with distilled water. The shrimp, crab and fish samples were taxonomically identified using standard reference sources by experts at the Department of Zoology of Obafemi Awolowo University, Ile-Ife Nigeria. Samples were stored separately at −20°C in a freezer. Sample identification --------------------- Two species of fishes were identified as Pomadasys jubelini, (common name: grunter) *([Figure 2](#i2156-9614-9-24-191204-f02){ref-type="fig"})* and Drepane africana, (local name: akaraba) *([Figure 3](#i2156-9614-9-24-191204-f03){ref-type="fig"})*. The crab was identified to be the male species of Callinectes amnicola, (common name: marine blue crab) *([Figure 4](#i2156-9614-9-24-191204-f04){ref-type="fig"})*, the shrimp was identified as Penaeus notialis, (common name: pink shrimp) *([Figure 5](#i2156-9614-9-24-191204-f05){ref-type="fig"})*. The sampled fish, shrimp, and crab were identified as either demersal, benthopelagic or pelagic species. ![Pomadasys jubelini (grunter) sample from Atlas Cove](i2156-9614-9-24-191204-f02){#i2156-9614-9-24-191204-f02} ![Drepane africana (spadefish) sample from Atlas Cove](i2156-9614-9-24-191204-f03){#i2156-9614-9-24-191204-f03} ![Callinectes amnicola (blue marine crab) sample from Atlas Cove](i2156-9614-9-24-191204-f04){#i2156-9614-9-24-191204-f04} ![Penaeus notialis (pink shrimp) sample from Atlas Cove](i2156-9614-9-24-191204-f05){#i2156-9614-9-24-191204-f05} ### Ecology and habitat of Pomadasys jubelini and Drepane Africana Pomadasys jubelini is found in sandy and muddy bottoms in coastal waters and estuaries and occurs in freshwater and brackish waters. It feeds on fish, small crustaceans, and mollusks.[@i2156-9614-9-24-191204-b17] It is a bottom-living, but periodically pelagic species usually inhabiting littoral waters to about 25 m depth, but has been reported to extend down to about 90 m. It is locally abundant in shallow waters throughout its range. Drepane africana is a neritic, coastal species and occurs in lagoon and estuarine habitats over sandy and muddy substrata between 20 and 50 cm depth. It feeds on fish eggs, benthic invertebrates, and detritus.[@i2156-9614-9-24-191204-b18] ### Ecology and habitat of Callinectes amnicola and Penaeus notialis Callinectes amnicola (blue marine crab) is a genus of crab from the family Portunidae usually found in the lagoon. The crabs may be considered as euryphagous, feeding on fishes, mollusks, crustaceans, higher plant materials, algae and diatoms. It is found in sand and ocean bottoms.[@i2156-9614-9-24-191204-b19] Penaeus notialis (pink shrimp) is a species of shrimp known to feed on diatoms, green algae, plants materials, as well as crustaceans and fish fragments. It spends a part of its life cycle in open water (ocean), but is mostly found in estuaries, lagoons, open sea and creeks. Its primary habitat (especially adults) is sand, sand- shell or coral- mud bottoms from intertidals.[@i2156-9614-9-24-191204-b20] Sample pre-treatment -------------------- Sediment samples were air dried for several days, after which stones and debris were removed from the samples and then pulverized and passed through a 2-mm mesh sieve to remove other unwanted materials. Samples for PAH analyses were further sieved through 0.5-mm mesh sieve and stored in foil papers until extraction was performed. The fish samples were allowed to thaw, the scales were removed and washed with running water and then distilled water before dissecting and removing the flesh and other parts which were put in sample bottles. Samples included fillets containing only fleshy parts and whole fish, including bone, fleshy parts and organs. The fish samples were weighed using an analytical weighing balance (wet weight) and homogenized with anhydrous sodium sulphate in a mortar with pestle. The mixture was labeled and wrapped in aluminum foil. It was left till the next day to cake, prior to extraction. Reference standards ------------------- Standard mix solutions of the United State Environmental Protection Agency\'s (USEPA) 16 priority PAHs, each at 100 μg/L in dichloromethane, were purchased from Sigma-Aldrich (St. Louis, MO, USA). The surrogate standard was a mixture containing naphthalene-d~8~ (N-d~8~), acenaphthene-d~10~ (Ace-d~10~), phenanthrene-d~10~ (Phen-d~10~), chrysene-d~12~ (Ch-d~12~) and perylene-d~12~ (Per-d~12~), which was added to the samples before extraction and used as internal standards for quantification. Stock solutions were used to prepare working standard solutions for calibration and spiking experiments. Extraction procedure for PAHs in sediment and aquatic organisms --------------------------------------------------------------- Polycyclic aromatic hydrocarbons in sediment samples were extracted using a Soxhlet extraction according to the method described by the Association of Official Analytical Chemists.[@i2156-9614-9-24-191204-b21] Five (5) g of each sediment sample was weighed and 5 g of anhydrous sodium sulphate was added to each sample. The samples were placed in a cellulose thimble and extracted for 16 to 24 hours using 150 ml of dichloromethane in a Soxhlet extractor. The extract was concentrated by evaporation overnight in a fume cupboard and covered with a perforated aluminum foil. Polycyclic aromatic hydrocarbons in the biota samples were determined according to the method of USEPA 3540C.[@i2156-9614-9-24-191204-b22] A total of 5 g of each species of shrimp, crab and fish samples that had been previously homogenized with anhydrous sodium sulfate were poured into 100 ml beakers and 40 ml of n-hexane and dichloromethane (1:1 vol/vol) was used as an extracting solvent. The beaker with the content was placed on a magnetic stirrer and shaken for about 25 minutes. The extract was decanted into a clean conical flask, then 20 ml of fresh solvent was added, and the process repeated. The extracts were combined and filtered through a small glass funnel containing a layer of anhydrous sodium sulphate over a plug of glass wool into a receiving conical flask. The extracts were concentrated by allowing to stand overnight in a fume cupboard and covered with perforated aluminum foil. Sample clean-up was carried out for both sediment and biota using USEPA Method 3630C.[@i2156-9614-9-24-191204-b23] A 600 × 19 mm clean up column was prepared. The hole was blocked with glass wool, 3 g of activated silica gel (60 mesh) was added and the column was topped with sodium sulfate. The column was rinsed by eluting with 20 ml n-hexane and discarded. The concentrated extract was loaded onto the prepared column and eluted with 50 ml n-hexane. The eluates were then concentrated to 1 ml using a rotary evaporator under a gentle stream of pure nitrogen. One (1) ml of the extract was then transferred into a well labeled vial and stored at 4°C prior to gas chromatograph mass spectrometry analysis. Instrumental and analytical conditions -------------------------------------- Analyses of PAHs were performed for both sediment and biota samples using a gas chromatograph mass spectrometer with selected ion monitoring (Shimadzu QP 2010 gas chromatograph mass spectrometry equipped with AOC 5000 auto injector). The column used was a Varian Factor Four fused silica capillary column (30 m × 0.25 mm × 0.25 μm film thickness) for separating target analytes. Helium was used as the carrier gas at a flow rate of 1.2 mL/min. The sample injector temperature was set at 250°C and 300°C and samples were injected at a volume of 1 mL in splitless mode. An initial column temperature of 60°C was held for 1 min and ramped from 60°C to 200°C at 10°C/min held for 2 min and finally to 300°C at 10°C/min and held for 6 min. The mass spectrometry conditions were set as follows: ionization source: electron ionization at -- 70 eV: ion source temperature: 200°C: store mass range m/z 47 - 400 μm. Identification of the individual PAHs was based on comparison of retention time between samples and standard solutions. Quality control --------------- The blanks were treated the same way as the samples. Sediment and biota samples were spiked. These fortified matrices were used as calibration standards, and the range of concentrations added to both sediment and biota matrices were used to produce the calibration curves of 20 - 100 mgkg^−1^. The surrogate internal standards were added to the spiked sediment and biota samples at 100 mgkg^−1^. The response factors were then calculated using the response obtained from desorption of a standard solution containing 40 mgkg^−1^ of the 16 PAHs of interest and 100 mgkg^−1^ of each internal standard. Spiked samples were extracted and analyzed. Recovery yields were 75 - 110% and limit of detection for individual PAHs ranged from 0.02 to 30.00 mgkg^−1^ in sediment and biota with a signal to noise ratio of three (3) and limit of quantization of signal to noise ratio of ten (10). Human health risk assessment ---------------------------- Toxicological risks associated with PAH concentrations in the biota samples were assessed through comparison of the observed concentrations with regulatory limits and guidelines. ### Potential human health risk To assess human health risks from exposure to PAHs through consumption of possibly contaminated biota samples (dietary intake), the dietary daily intake concentrations of PAH\'s from consumption of contaminated shrimps, crabs and fish species were determined. The dietary daily intake of PAHs in contaminated biota samples were assessed for the adult population using [Equations 1](#i2156-9614-9-24-191204-e01){ref-type="disp-formula"}, [2](#i2156-9614-9-24-191204-e02){ref-type="disp-formula"} and [3](#i2156-9614-9-24-191204-e03){ref-type="disp-formula"}. The daily intake of PAHs from the biota samples was calculated by multiplying the respective PAH concentration in each sample by the consumption rate of an average weight adult (70 kg). where, 0.0685 kg/day is based on the assumption that an average Nigerian consumes 25 kg of fish per annum and an average of 0.0016 and 0.0219 kg/day of crabs and shrimp, respectively.[@i2156-9614-9-24-191204-b5],[@i2156-9614-9-24-191204-b15] ### Carcinogenic risk assessment of polycyclic aromatic hydrocarbons in biota samples Cancer risk due to dietary exposure to PAHs in fish was assessed. The carcinogenic potencies of individual PAHs were evaluated by multiplying the PAH concentrations in the sample by the individual toxicity equivalency factor (TEF) as shown in [Equation 4](#i2156-9614-9-24-191204-e04){ref-type="disp-formula"}.[@i2156-9614-9-24-191204-b24] The toxicity equivalency factor is an estimate of the relative toxicity of individual PAH fractions compared to benzo(a)pyrene. Toxic equivalency factors have been applied as useful tools for the regulation of compounds with common mechanisms of action (e.g. PAHs). The TEFs developed by Nisbet and LaGoy were applied and these values were used to calculate PAH as equivalents for benzo\[a\]pyrene for a standard adult with 70 kg body weight.[@i2156-9614-9-24-191204-b25] The toxic equivalent quotient (TEQ) was derived by adding the carcinogenic potencies of individual PAHs shown in [Equation 5](#i2156-9614-9-24-191204-e05){ref-type="disp-formula"}.[@i2156-9614-9-24-191204-b24] where, B(A)Pteq is the carcinogenic potencies of individual PAHs and C~i~ is the PAH concentration. The screening value (SV) was calculated as shown in [Equation 6](#i2156-9614-9-24-191204-e06){ref-type="disp-formula"}, and then compared with the estimated TEQ value to assess the health risk of PAHs associated with consumption of the biota samples. The screening value is referred to as the threshold concentration of chemicals in edible tissue(s) that is of potential risk to consumers. It was calculated using the formula of Nozar *et al*.[@i2156-9614-9-24-191204-b5] where, RL is the maximum acceptable risk level (10^−5^),CSF is the oral cancer slope factor (7.3 mg/kg/day), BW is body weight (70 kg)\*, and CONR is the fish consumption rate. *\*Body weight of 70 kg applies to the adult population.*[@i2156-9614-9-24-191204-b15] Histopathological examination ----------------------------- The fish samples were dissected to remove the target organs, while the shrimps and crabs were dissected to obtain the fleshy parts. The gills, fillet, liver of fish and the fleshy parts of the crab and shrimp were put in a separate well labeled bottle, fixed in 5% formalin for at least 48 hours and transferred into a sampling bottle rack. Tissue processing for the histopathological analyses was done according to standard methods.[@i2156-9614-9-24-191204-b26] The tissues were removed from the fixative, and samples were rinsed in tap water for 5 minutes, and dehydrated in ascending ethanol concentrations (70%, 80% and 90% alcohol) for a minimum of 2 minutes each. The dehydrated tissues were cleaned in a wax miscible agent (xylene) for 2 minutes and then embedded in paraffin. Tissue sectioning and staining ------------------------------ The fish tissues were then cut into sections approximately 5 μm thick from the block using a rotary microtome (Yamato Kohki, serial no: 75010JO). The cut samples were dried in a hot air oven to remove moisture and each section was mounted on a glass slide. The sections were de-waxed in a wax-miscible agent and rehydrated through descending concentrations of ethanol (90%, 80% and 70% alcohol) for at least 2 minutes each. The sections were then stained with hematoxylin and eosin, after which the tissues were placed in hematoxylin solution for 3 minutes and aqueous eosin for 3 minutes, mounted on a slide and covered with cover slip and labeled.[@i2156-9614-9-24-191204-b27] The tissues were examined, and their microphotographs were taken using a digital binocular compound LED microscope (model MD827S30L series). Statistical analysis -------------------- The obtained data were subjected to descriptive statistics and analysis of variance. The significant treatment means were separated using Duncan\'s multiple range tests using the Statistical Package for the Social Sciences software (SPSS) version 19.0. Results ======= Concentrations of PAHs in sediment samples are presented in [Table 1](#i2156-9614-9-24-191204-t01){ref-type="table"}. A total of 17 PAHs compounds (naphthalene, 1-methylnaphthalene, 2-methylnaphthalene, acenaphthylene acenaphthene, fluorene, phenanthrene, anthracene, pyrene, fluoranthene, benzo(a)anthracene, chrysene, benzo(b)fluoranthene, benzo(k) fluoranthene, benzo(a)pyrene, indeno(1,2,3-cd) pyrene, benzo(ghi) perylene) were detected in the sediment samples. Concentration of PAHs ranged from 2.15 - 36.46 mgkg^−1^ across the sampling points. Sampling point 5 had the highest (36.46 mg/kg) concentration of PAHs compared to those detected from other points. In the present study, 47.06% of PAHs had 2--3 rings, 23.53% of PAHs had 4-rings, and 29.41% of PAHs had 5--6 rings. The percentage composition pattern of PAHs detected in the sediment samples by number of rings is presented in [Table 2](#i2156-9614-9-24-191204-t02){ref-type="table"}. The phenanthrene to anthracene (Ph/An) ratio for sediment samples were 0.65, 2.43 and 1.72 in sampling points 1, 4 and 5, respectively, but were below detection limit in points 2 and 3. The respective values for fluoranthene to pyrene (Fl/Py) ratio were 0.38, 0.66, 0.47 and 1.02 in sampling points 1, 2, 4, and 5, respectively. ###### Concentrations of PAHs in Sediment (mg/kg) PAHs Sampling locations ------------------------ -------------------- -------------- --------------- --------------- -------------- Naphthalene 1.03±0.12^a^ 1.17±0.01^a^ 0.95±0.00^ab^ 0.70±0.00^c^ 0.66±0.01^c^ 1-Methylnaphthalene 0.36±0.03^a^ 0.41±0.02^a^ 0.31±0.03^a^ 0.19±0.02^ab^ 0.23±0.00^a^ 2-Methylnaphthalene 0.23±0.06^a^ 0.27±0.01^a^ 0.19±0.03^a^ 0.15±0.03^a^ 0.12±0.00^a^ Acenaphthylene 1.42±1.11^a^ BDL BDL BDL 0.45±0.13^b^ Acenaphthene 0.23±0.19^a^ 0.09±0.01^b^ 0.03±0.01^b^ 0.04±0.01^b^ 0.05±0.01^b^ Fluorene 1.05±0.53^a^ BDL BDL BDL BDL Phenanthrene 2.00±0.19^a^ BDL BDL 0.17±0.02^c^ 0.74±0.07^b^ Anthracene 3.25±0.14^a^ BDL BDL 0.07±0.01^c^ 0.43±0.07^b^ Pyrene 5.43±0.18^a^ 0.97±0.04^c^ BDL 0.49±0.00^d^ 4.63±2.30^b^ Fluoranthene 2.07±0.08^b^ 0.64±0.02^d^ 1.63±0.01^c^ 0.23±0.02^e^ 4.73±2.10^a^ Benzo(a)anthracene 0.76±0.66^b^ BDL BDL 0.11±0.01^c^ 2.48±0.45^a^ Chrysene BDL BDL BDL BDL 4.97±2.45 Benzo(k)fluoranthene BDL BDL BDL BDL 3.03±1.44 Benzo(b)fluoranthene BDL BDL BDL BDL 2.80±1.67 Benzo(a)pyrene BDL BDL BDL BDL 4.10±1.95 Benzo(ghi)perylene BDL BDL BDL BDL 3.38±1.89 Dibenzo(a,h)anthracene BDL BDL BDL BDL BDL Indeno(1,2,3-cd)pyrene BDL BDL BDL BDL 3.67±2.34 ∑CPAHs 0.76 \- \- 0.11 20.76 Total PAHs 17.82 3.55 3.11 2.15 36.46 ^\*^Mean concentrations with different superscripts along the same row are significantly different (P≤0.05). Abbreviations: BDL, below detection limit (detection limit − 0.001 mg/kg); CPAHS, carcinogenic PAH. ###### Percentage Composition of LMW and HMW of Total PAHs Detected in Sediment Samples Number of Rings \% Abundance ----------------- -------------- 2--3 ring PAHs 47.06% 4 ring PAHs 29.41% 5--6 ring PAHs 23.53% Polycyclic aromatic hydrocarbon concentrations in Drepane africana and Pomadasys jubelini ----------------------------------------------------------------------------------------- Concentration of PAHs in Drepane africana and Pomadasys jubelini samples are presented in [Table 3](#i2156-9614-9-24-191204-t03){ref-type="table"}. The concentration of total PAHs in the fillet (i.e. muscle) was 22.67 mg/kg, and 33.97 mg/kg in the whole fish in Drepane africana. For the individual PAH compounds, naphthalene had the highest concentration (28.53±9.19 mg/kg) which was observed in the whole fish sample, while anthracene had the lowest concentration (0.02±0.01 mg/kg) and was observed in the fillet of the fish sample. ###### Mean Concentrations of PAHs in Drepane africana and Pomadasys jubelini (mg/kg) PAHs Drepane africana Pomadasys jubeli ------------------------ ------------------ ------------------ -------------- ---------------- Naphthalene 19.17±20.13^b^ 28.53±9.19^a^ 9.44±3.42^b^ 27.60±12.20^a^ 1-MethylNaphthalene 1.46±0.86^b^ 1.74±0.06^a^ 0.76±0.68^b^ 2.54±2.04^a^ 2-MethylNaphthalene 0.93±0.47^a^ 1.05±0.36^a^ 0.45±0.37^b^ 1.71±1.33^a^ Acenaphthylene 0.07±0.12^a^ 0.24±0.04^a^ 0.15±0.13^a^ 0.33±0.11^a^ Acenaphthene 0.22±0.17^a^ 0.14±0.11^a^ 0.15±0.13^b^ 0.54±0.33^a^ Fluorene 0.34±0.30^a^ 0.20±0.17^ab^ 0.10±0.11^b^ 0.50±0.46^a^ Phenanthrene 0.25±0.21^ab^ 0.70±0.62^a^ 0.39±0.11^b^ 0.91±1.01^a^ Anthracene 0.02±0.01^a^ 0.17±0.16^a^ 0.08±0.06^a^ 0.02±0.01^a^ Pyrene 0.07±0.03^b^ 0.52±0.43^a^ 0.17±0.05^b^ 0.40±0.25^a^ Fluoranthene 0.14±0.11^b^ 0.69±0.44^a^ 0.20±0.07^b^ 0.48±0.35^a^ Benzo(a)anthracene BDL BDL BDL BDL Chrysene BDL BDL BDL BDL Benzo(k)fluoranthene BDL BDL BDL BDL Benzo(b)fluoranthene BDL BDL BDL BDL Benzo(a)pyrene BDL BDL BDL BDL Benzo(ghi)perylene BDL BDL BDL BDL Dibenzo(a,h)anthracene BDL BDL BDL BDL Indeno(1,2,3-cd)pyrene BDL BDL BDL BDL Total PAHs 22.67 33.97 11.89 35.02 ^\*^Mean concentrations with different superscripts along the same row are significantly different at P≤0.05. Abbreviation: BDL, below detection limit (detection limit − 0.001 mg/kg) Moreover, the concentration of total PAHs in the fillet was 11.89 mg/kg and 35.02 mg/kg in the whole fish in Pomadasys jubelini samples. A total of 10 PAH compounds were detected in the samples. Naphthalene had the highest concentration (27.60±12.20 mg/kg) of individual PAH compounds and was observed in the whole fish sample, while anthracene had lowest concentration (0.02±0.01 mg/kg) and was observed in the whole fish sample. In the present study, 80% of PAHs had 2--3 rings, 20% had 4-rings, and no PAHs with 5--6 rings were detected in Drepane africana and Pomadasys jubelini samples *([Table 4](#i2156-9614-9-24-191204-t04){ref-type="table"})*. ###### Percentage composition of LMW and HMW of total PAHs detected in Drepane africana and Pomadasys jubelini Number of rings \% Abundance ----------------- -------------- 2--3 ring PAHs 80% 4 ring PAHs 20% Polycyclic aromatic hydrocarbon concentrations in Callinectes amnicola (blue marine crab) and Penaeus notialis (pink shrimp) ---------------------------------------------------------------------------------------------------------------------------- Concentrations of PAHs in Callinectes amnicola and Penaeus notialis samples are presented in [Table 5](#i2156-9614-9-24-191204-t05){ref-type="table"}. A total of 9 PAHs were detected in C. amnicola, while 10 PAH congeners (naphthalene, 1-methylnaphthalene, 2-methylnaphthalene, acenaphthylene, acenaphthene, fluorene, phenanthrene, anthracene, pyrene, fluoranthene) were detected in P. notialis. All of the LMW PAHs tested for were present except for fluorene, which was not detected in crab. The concentration of total PAHs in the crab sample was 60.30 mg/kg. The highest concentration (46.50±15.66 mg/kg) of individual PAH compounds were obtained in naphthalene and the lowest concentration (0.05±0.02 mg/kg) was obtained in anthracene. The result obtained in this study (6 0030 ng/g) for crab was higher than the result reported for crab; young (1 2138.07 ng/g) and mature crabs with eggs (5629.80 ng/g) collected from Lagos lagoon.[@i2156-9614-9-24-191204-b28] In the present study, 77.78% of PAHs had 2--3 rings, 22.22% of PAHs had 4-rings, and no 5--6 ring PAHs were detected in Callinectes amnicola and Penaeus notialis samples. Concentration of PAHs in shrimp ranged from 0.08±0.13 to 50.65 ± 21.88 mgkg^−1^. The highest concentration was found in naphthalene and lowest concentration was found in acenaphthylene.[@i2156-9614-9-24-191204-b29]The percentage composition pattern of PAHs detected in the samples by the number of rings is shown in [Table 6](#i2156-9614-9-24-191204-t06){ref-type="table"}. ###### Concentrations of PAHs in Callinectes amnicola and Penaeus notialis (mg/kg) Wet Weight PAHs Crab Shrimp ------------------------- ---------------- ---------------- Naphthalene 46.50±15.66^b^ 50.65±21.88^a^ 1-Methylnaphthalene 7.01±8.38^a^ 6.57±7.82^b^ 2-Methylnaphthalene 4.70±5.94^a^ 4.21±5.27^b^ Acenaphthylene 0.18±0.16^a^ 0.08±0.13^a^ Acenaphthene 0.29±0.15^b^ 1.31±1.72^a^ Fluorene BDL 1.78±3.07 Phenanthrene 0.79±1.02^b^ 1.65±2.04^a^ Anthracene 0.05±0.02^b^ 3.34±2.10^a^ Pyrene 0.27±0.16^b^ 0.57±0.59^a^ Fluoranthene 0.51±0.29^b^ 0.91±1.20^a^ Benzo(a)anthracene BDL BDL Chrysene BDL BDL Benzo(k)fluoranthene BDL BDL Benzo(b)fluoranthene BDL BDL Benzo(a)pyrene BDL BDL Benzo(ghi)perylene BDL BDL Dibenz(a,h)anthracene BDL BDL Indeno(-1,2,3-cd)pyrene BDL BDL Total PAHs 60.30 71.06 ^\*^Mean concentrations with different superscripts along the same row are significantly different at P≤0.05. Abbreviation: BDL, below detection limit (detection limit − 0.001 mg/kg) ###### Percentage composition of PAHs in samples of Callinectes amnicola and Penaeus notialis Number of Rings \% Abundance ----------------- -------------- 2--3 ring PAHs 77.78% 4 ring PAHs 22.22% Health risk assessment ---------------------- The estimated dietary intake values of total PAHs for fillet and whole fish were 1.55 and 2.33 mg/kg body weight/day, respectively. The fish consumption rate was set at 0.0685 kg/day from the annual per capita fish consumption of 25 kg for Nigeria.[@i2156-9614-9-24-191204-b15] The values obtained in this study exceeded the values reported for fish samples from Degele community, Sapele, Nigeria which was reported to be 0.02 - 0.94 mg/kg body weight/day (O. niloticus), 0.02--0.12 mg/kg body weight/day (C. gariepinus), 0.12--0.16 mg/kg body weight/day (H. longifilis) and 0.14--0.58 mg/kg body weight/day (L. falcipinnis), respectively.[@i2156-9614-9-24-191204-b30] The estimated dietary intakes of sampled fish species are shown in [Table 7](#i2156-9614-9-24-191204-t07){ref-type="table"}. ###### Estimated Dietary Intake of PAHs from Sampled Organisms Organisms Estimated dietary Intake (mgkg; body weight/day) ----------------------------- -------------------------------------------------- Drepane Afrieana (fillet) 1.55 Drepane Afrieana (whole) 2.33 Pomadasys jubelini (fillet) 0.81 Pomadasys jubelini (whole) 2.40 Crab 0.10 Shrimp 1.56 Dietary intake of polycyclic aromatic hydrocarbons from Callinectes amnicola and Penaeus notialis ------------------------------------------------------------------------------------------------- The estimated dietary intake values of total PAHs for crab and pink shrimp were 0.10 and 1.56 mg/kg body, respectively. The carcinogenic potencies of individual PAHs and TEQ values are presented in [Table 8](#i2156-9614-9-24-191204-t08){ref-type="table"}. The TEQ values obtained from TEF values were used to assess the carcinogenicity of PAH contamination in the sampled biota.[@i2156-9614-9-24-191204-b31] The TEQ values of PAHs in the biota samples were 6.08×10^−2^, 1.01×10^−1^, 2.29×10^−2^, 3.55 × 10^−2^, 1.26×10^−2^ and 3.52×10^−2^ mg/kg for crab, shrimp, Drepane africana (fillet), Drepane africana (whole), Pomadasys jubelini (fillet), Pomadasys jubelini (whole), respectively. ###### Carcinogenic Potencies of Individual PAHs and Toxic Equivalent Quotient Values B(a)Pteq values (mg/kg) ------------------------- ------- ------------- ------------- -------------- ------------- ------------- ------------- Naphthalene 1- 0.001 4.67×10^−2^ 5.06×10^−2^ 1.92×10^−2^ 2.85×10^−2^ 9.44×10^−3^ 2.76×10^−2^ Methylnaphthalene 2- 0.001 7.00×10^−3^ 6.57×10^−3^ 1.46×10^−3^ 1.74×10^−3^ 7.60×10^−4^ 2.54×10^−3^ Methylnaphthalene 0.001 5.00×10^−3^ 4.21×10^−3^ 9.30×10^−4^ 1.05×10^−3^ 4.50×10^−4^ 1.71×10^−3^ Acenaphthylene 0.001 1.8×10^−4^ 8.00×10^−5^ 7.00×10^−5;^ 2.40×10^−4^ 1.50×10^−4^ 3.30×10^−4^ Acenaphthene 0.001 2.9×10^−4^ 1.31×10^−3^ 2.20×10^−4^ 1.40×10^−3^ 1.50×10^−4^ 5.40×10^−4^ Fluorene 0.001 \- 1.78×10^−3^ 3.40×10^−4^ 2.00×10^−4^ 1.00×10^−4^ 5.00×10^−4^ Phenanthrene 0.001 7.9×10^−4^ 1.65×l0^−3^ 2.50×10^−4^ 7.00×10^−4^ 3.90×10^−4^ 9.10×10^−4^ Anthracene 0.01 5.00×10^−4^ 3.34×10^−3^ 2.00×10^−4^ 1.70×10^−3^ 8.00×10^−4^ 2.00×10^−4^ Pyrene 0.001 2.70×10^−4^ 5.70×10^−4^ 7.00×10^−5^ 5.20×10^−4^ 1.70×10^−4^ 4.00×10^−4^ Fluoranthene 0.001 5.1 ×10^−4^ 9.10×10^−4^ 1.40×10^−4^ 6.90×10^−4^ 2.00×10^−4^ 4.80×10^−4^ TEQ (values mg/kg) 6.08×10^−2^ 1.01×10^−1^ 2.29×10^−2^ 3.55×10^−2^ 1.26×10^−2^ 3.52×10^−2^ Abbreviation: B(a)Pteq, carcinogenic potencies of individual PAHs Carcinogenic potency of individual polycyclic aromatic hydrocarbons and toxic equivalent quotient ------------------------------------------------------------------------------------------------- The carcinogenic potencies of individual PAHs and TEQ values are presented in [Table 8](#i2156-9614-9-24-191204-t08){ref-type="table"}. The TEFs method was developed to evaluate structurally related compounds and has been applied as a useful tool for the regulation of compounds with a common mechanism of actions (e.g. PAHs). The TEF is an estimate of the relative toxicity of an individual PAH fraction compared to benzo(a)pyrene. The TEF values are used to calculate other PAHs to benzo(a)pyrene equivalents (the most toxic PAHs) for an average adult with 70 kg body weight.[@i2156-9614-9-24-191204-b24] The carcinogenic potency of individual PAHs is represented by the value resulting from the product of the concentration and TEF value of each congener. The TEQ value is the summation of carcinogenic potencies of individual PAH values obtained from a particular sample. It expresses an aggregate measure of toxicity based on a number of contributing compounds. Screening value --------------- The SV was evaluated to assess the health risks posed by PAHs to humans from consuming the sampled organisms. The screening value is defined as the threshold concentration of chemicals in edible tissue that is of potential public health concern.[@i2156-9614-9-24-191204-b16],[@i2156-9614-9-24-191204-b32] An estimated SV of 0.0599, 0.0044 and 0.0014 mg/kg was obtained for crab, shrimp and fish samples, respectively. The resulting TEQ values obtained for the sampled biota exceeded the screening values *([Figure 6](#i2156-9614-9-24-191204-f06){ref-type="fig"})*. ![Comparison between TEQ and screening values](i2156-9614-9-24-191204-f06){#i2156-9614-9-24-191204-f06} Histopathological examination ----------------------------- In the present study, the major changes observed in the gills of Drepane africana and Pomadasys jubelini were hypertrophy of the primary lamellae and hyperplasia of the secondary lamellae. Shortening and fusion of the secondary lamellae were observed in Drepane africana, while hyperplasia of the epithelial cells was observed in Pomadasys jubelini. In the muscle of Drepane africana and Pomadasys jubelini, splitting and atrophy of the muscle bundles were observed, while necrosis of the muscle bundles was seen in Pomadasys jubelini only *([Figures 7a](#i2156-9614-9-24-191204-f07a){ref-type="fig"}--[c](#i2156-9614-9-24-191204-f07c){ref-type="fig"}).* Splitting of the muscle myofibrils was observed in shrimp only, while splitting and atrophy of the muscle bundles were observed in the muscles of shrimp and crab *([Figures 8a](#i2156-9614-9-24-191204-f08a){ref-type="fig"}--[b](#i2156-9614-9-24-191204-f08b){ref-type="fig"} and [9](#i2156-9614-9-24-191204-f09){ref-type="fig"})*. Changes observed in the liver of Drepane africana and Pomadasys jubelini included necrosis, hepatopancreas and cellular degeneration *([Figure 10a](#i2156-9614-9-24-191204-f10a){ref-type="fig"}--[d](#i2156-9614-9-24-191204-f10d){ref-type="fig"})*. ![Photomicrograph of muscle section in Drepane africana showing atrophy of muscle bundles (AMB) (Mag. ×100)](i2156-9614-9-24-191204-f07a){#i2156-9614-9-24-191204-f07a} ![Photomicrograph of muscle section in Drepane africana showing splitting of muscle (SMB) (Mag. ×400)](i2156-9614-9-24-191204-f07b){#i2156-9614-9-24-191204-f07b} ![Photomicrograph of muscle section in Pomadasys jubelini showing necrosis of muscle bundles (NMB) (Mag. ×100)](i2156-9614-9-24-191204-f07c){#i2156-9614-9-24-191204-f07c} ![Photomicrograph of muscle section in Penaeus notialis (pink shrimp) showing atrophy of muscle bundles (AMB) (Mag. ×40)](i2156-9614-9-24-191204-f08a){#i2156-9614-9-24-191204-f08a} ![Photomicrograph of muscle section in Penaeus notialis (pink shrimp) showing splitting of muscle (SMB), and splitting of muscle myofibril (SMM) (Mag. ×100)](i2156-9614-9-24-191204-f08b){#i2156-9614-9-24-191204-f08b} ![Photomicrograph of muscle section in Callinectes amnicola (blue marine crab) showing necrosis of muscle bundles (NMB) and splitting of muscle (SMB) (Mag. ×40)](i2156-9614-9-24-191204-f09){#i2156-9614-9-24-191204-f09} ![Photomicrograph of liver section in Drepane africana showing focal area hepatopancreas of necrosis (Mag. ×100) degeneration](i2156-9614-9-24-191204-f10a){#i2156-9614-9-24-191204-f10a} ![Photomicrograph of liver section in Drepane africana showing degeneration (HD) and cellular (CD) (Mag. ×100) degeneration](i2156-9614-9-24-191204-f10b){#i2156-9614-9-24-191204-f10b} ![Photomicrograph of liver section in Drepane africana showing focal area hepatopancreas degeneration (HD) (Mag. ×100)](i2156-9614-9-24-191204-f10c){#i2156-9614-9-24-191204-f10c} ![Photomicrograph of liver section in Drepane africana showing the nucleus (N) and hepacytes (H) (Mag. ×100)](i2156-9614-9-24-191204-f10d){#i2156-9614-9-24-191204-f10d} Discussion ========== The predominance of LMW and HMW PAHs in the sediments reflects the presence of significant combustion products from pyrolytic processes and/or petrogenic sources.[@i2156-9614-9-24-191204-b33],[@i2156-9614-9-24-191204-b34] The preponderance of LMW and HMW PAHs in the sediments indicates the presence of significant combustion products from pyrolytic processes and/or petrogenic sources. [@i2156-9614-9-24-191204-b33],[@i2156-9614-9-24-191204-b34] A sediment quality guideline of 1000 ng/g dry weight total PAHs was designed to protect estuarine fish against several important health effects.[@i2156-9614-9-24-191204-b35] Based on this guideline, the results of this study showed that the concentrations of total PAHs exceeded 1000 ng/g dry weight at all sampling points, indicating that aquatic organisms in the region could be at severe health and environmental risk. Polycyclic aromatic hydrocarbon concentrations in soil/sediment can be classified according to the following categories: \>1.0 mg/kg, 0.001 -- 1.0 mg/kg and \< 0.001 mg/kg for high risk, medium risk, and low risk, respectively.[@i2156-9614-9-24-191204-b36] In the present study, the concentration of PAHs from all sampling points were higher than 1.0 mg/kg, indicating that they presented a high risk. All sediment samples exceeded the USEPA guideline value of 2.5 mg/kg except sampling point 4, which was slightly lower (2.15 mg/kg) *([Table 1](#i2156-9614-9-24-191204-t01){ref-type="table"})*. In rural areas, PAHs adsorbed in atmospheric particles can be deposited on the surface of lakes, streams, and oceans by dry or wet deposition, where they could be dispersed by currents and eventually become integrated with sediment. Sediments near urban centers are influenced by atmospheric deposition of PAHs. Other sources of PAHs include storm and sanitary sewer effluents as well as roadway runoff. It was observed that the concentration of PAHs was higher in sediment samples than in water samples. This could be attributed to their hydrophobic tendencies and propensity towards adsorption to particles and solid phases. In addition, they settle and become part of the sedimentary record. Anthropogenic PAHs originate mainly from combustion of fossil fuels and spillage of petroleum products; from fuel combustion (pyrolytic) or from crude oil (petrogenic). Contamination may be identified by ratios of individual PAH compounds based on peculiarities in PAH composition and distribution patterns as a function of the emission source. Ratios of Ph/An and Fl/Py have been widely used to distinguish petrogenic and pyrogenic sources of PAHs.[@i2156-9614-9-24-191204-b37],[@i2156-9614-9-24-191204-b38] Polycyclic aromatic hydrocarbons of petrogenic origin are generally characterized by Ph/An values \> 10, whereas combustion processes often result in low Ph/An ratio \< 10. For the Fl/Py ratio, values \> 1 have been used to indicate pyrolytic origins and values \< 1 are attributed to petrogenic sources. The results from both Ph/An and Fl/Py ratios indicated that PAHs in the Atlas Cove jetty area may originate from both pyrolytic and petrogenic sources. It was observed that the PAHs have pyrolytic sources in sediment samples in all sampling points and this may be attributed to high ship traffic. Potential toxicity of PAHs in sediments on the surrounding aquatic organisms was assessed. The PAHs concentration in the sediments were compared with US National Oceanic sediment quality guidelines *([Table 9](#i2156-9614-9-24-191204-t09){ref-type="table"})*.[@i2156-9614-9-24-191204-b39] The recommended effect range low (ERL) and effect range median (ERM) target values were used to determine toxic effects in the sampling locations. When PAH concentrations vary between ERL and ERM values, a mild toxic effect is expected. In addition, no negative effect is expected for PAH concentrations lower than ERL values. [Table 9](#i2156-9614-9-24-191204-t09){ref-type="table"} indicates a high probability of risk for organisms that live in sampling locations 1 and 5. Naphthalene, acenaphthene, and fluoranthene exceeded the ERL values, but were within ERM values in both sampling locations, indicating a mild toxic effect. Anthracene exceeded the ERL and ERM values at sampling locations 1 and 5, but was within ERM value at sampling location 5. Anthracene, phenanthrene, pyrene and fluoranthene were below ERL values in sampling location 4. Anthracene, fluorene, phenanthrene, acenaphthylene and pyrene in sampling location 1 and pyrene and benzo(a)pyrene in sampling location 5 exceeded ERM values, suggesting that adverse biological effects such as cancer, reproductive and physiological disorder may occur in fish and mammals.[@i2156-9614-9-24-191204-b40] ###### Concentrations of PAHs in Sediment Compared with US National Oceanic Sediment Quality Guidelines PAHs ERL[@i2156-9614-9-24-191204-b39] (ngg-^1^) ERM[@i2156-9614-9-24-191204-b39] (nss-^1^) Sampling locations ------------------------ -------------------------------------------- -------------------------------------------- -------------------- ------ ------ ----- ------ Naphthalene 160 2100 1030 1170 950 700 660 Anthracene 85 1100 3250 \- \- 70 430 Fluorene 19 540 1050 \- \- \- \- Phenanthrene 240 1500 2000 \- \- 170 740 Acenaphthene 16 500 230 90 30 40 50 Acenaphthylene 44 640 1420 \- \- \- 450 Pyrene 665 2600 5430 970 1630 490 4630 Fluoranthene 600 5100 2070 640 \- 230 4730 Benzo (b) fluoranthene \- \- \- \- \- \- 2800 Benzo(a) pyrene 430 2800 \- \- \- \- 4100 Abbreviations: ERL, effective range low; ERM, effective range median. Polycyclic aromatic hydrocarbons concentrations in Drepane africana and Pomadasys jubelini ------------------------------------------------------------------------------------------ A total of 10 PAH compounds (naphthalene, 1-methylnaphthalene, 2-methylnaphthalene, acenaphthylene, acenaphthene, fluorene, phenanthrene, anthracene, pyrene, fluoranthene) were detected in the samples *([Table 3](#i2156-9614-9-24-191204-t03){ref-type="table"})*. The less carcinogenic LMW PAHs were detected with naphthalene and its substituent present in the fish samples. The more carcinogenic HMW PAHs (benzo(a)anthracene, chrysene, benzo(k)fluoranthene, benzo(b)fluoranthene, benzo(ghi) perylene, dibenzo(a,h)anthracene, indeno(1,2,3-cd)pyrene) were not detected in the samples of Drepane africana. This result agreed with the report of PAHs in fish samples from the Degele community of Delta state, Nigeria and the bioaccumulation of PAHs in fish and invertebrates of Lagos lagoon.[@i2156-9614-9-24-191204-b30],[@i2156-9614-9-24-191204-b41] A significant (P≤0.05) difference was observed in the total PAH concentrations between fillet and whole fish of the fish species. The percentage composition pattern of PAHs detected in the samples by number of rings is shown in [Table 4](#i2156-9614-9-24-191204-t04){ref-type="table"}. The predominance of LMW PAHs as compared to HMW PAHs in the fish samples reflects the presence of significant petrogenic processes.[@i2156-9614-9-24-191204-b33],[@i2156-9614-9-24-191204-b34] The analysis showed that a total of 10 PAHs (8 of which are among the 16 PAHs prioritized by the USEPA) were present in the fish sample. The concentration of PAHs in fish was higher than the water column; this could be due to the fact that PAHs are more readily absorbed by fish than other aquatic organisms on exposure to contaminated materials, thus attaining elevated levels compared to those in the surrounding medium.[@i2156-9614-9-24-191204-b6] The trend for the less carcinogenic LMW PAHs and the more carcinogenic HMW PAHs in Pomadasys jubeli was similar to that observed in Drepane africana presented above. The concentration of total PAHs was lower in the whole fish and fillet of both fish species compared to that of crab and shrimp in the present study. This may be because fish have been reported to have physiological mechanism(s) of rapid PAH biotransformation or depuration and could be influenced by various factors, such as chemical exposure route and time, lipid content of tissues, environmental factors, exposure to multiple contaminants, and differences in species, age, sex, and health conditions of the test animals.[@i2156-9614-9-24-191204-b28] The biotransformation of hydrophobic-containing substances in fish is a major determinant of its toxicity, distribution and excretability.[@i2156-9614-9-24-191204-b6] A large percentage of the world\'s population depends on seafood, especially fish, to meet their nutritional requirements. In Nigeria, fish provides over 60% of protein intake and is recognized as a very important source of animal protein. Food consumption has been identified as an important pathway of human exposure to many contaminants, including PAHs. Due to the lipophilic nature and high chemical stability of PAHs, they accumulate in the fatty tissues of fish following their uptake.[@i2156-9614-9-24-191204-b42] Exposure pathways of PAHs to fish include bioconcentration from water across their gills, skin and ingestion of PAH-contaminated particulate matter along with food, as PAHs readily adsorb onto particulate organic matter especially soil sediments.[@i2156-9614-9-24-191204-b15] The concentrations of contaminants such as PAHs in fish reflect the state of contamination of the environment.[@i2156-9614-9-24-191204-b43] The observed concentrations of total PAHs in fish in this study indicate high levels of PAHs contamination around the Atlas Cove jetty. Polycyclic aromatic hydrocarbon concentrations in Callinectes amnicola (blue marine crab) ----------------------------------------------------------------------------------------- Crabs have been reported to have high lipid contents and this increases the chance of absorbing more hydrocarbon molecules, especially those that are not easily degraded or eliminated. The higher concentration of PAHs observed in the present study may be due to the proximity of the sampling points to the Atlas Cove jetty or the movement of ships along the waterways which may serve as a source of pollution. However, PAH concentrations were lower than the values (101.10 - 151.49 μg/g) reported for crabs (Callinectes sapidus) obtained from the coastal area of Ondo State, Nigeria.[@i2156-9614-9-24-191204-b29] The higher levels of PAHs in shrimps are presumably due to food chain bioaccumulation and can be harmful to human health. The concentration of PAHs in crab and shrimp were significant and may have wide environmental implications, affecting bioconcentration in their tissues due to their inability to metabolize PAHs efficiently. The relatively higher concentrations of total PAHs in tissues of shellfish than fish showed the bioaccumulative potency of PAHs by the studied organisms. It may also be due to the fact that shrimps and crabs live directly on and forage in the sediments, whereas fish live up in the water column. Several aquatic organisms such as bivalves, crabs, and shrimps have been reported to bioaccumulate and bioconcentrate organic pollutants in their target organs at levels higher than background concentrations.[@i2156-9614-9-24-191204-b44],[@i2156-9614-9-24-191204-b45] Therefore, they are excellent bioaccumulators of organic and inorganic pollutants. Higher concentrations of total PAHs in banana shrimp and blue crab were compared to Drepane punctata and Pomadasys kaakan, which had lower concentrations of PAHs.[@i2156-9614-9-24-191204-b5] Health risk assessment ---------------------- The consumption of Drepane africana at the rate of 68 g/day may induce adverse health effects over time in consumers. Dietary intake of *polycyclic aromatic hydrocarbons from* Pomadasys jubelini ---------------------------------------------------------------------------- The estimated dietary intake values in the present study (0.81 for fillet and 2.40 mg/kg body weight/day for whole fish) were considerably higher in comparison with values reported in other countries of 1.77 - 10.7 ng/kg body weight/day, 626 - 712 ng/day, 13.8 - 16.7 ng/kg body weight/day and 231 ng/day for Mumbai, India, Spain, Korea and Kuwait, respectively.[@i2156-9614-9-24-191204-b33],[@i2156-9614-9-24-191204-b46],[@i2156-9614-9-24-191204-b47] Comparison of toxic equivalency quotient values ----------------------------------------------- The lowest TEQ value was obtained in the fillet of Pomadasys jubelini. The TEQ values of PAHs in fish species, as reported by Tongo *et al.* were 0.22, 0.005, 0.30 and 0.03 mg/kg in Clarias gariepinus, Tilapia zilli, Ethmalosa fimbriata, and Scomber scombrus, respectively.[@i2156-9614-9-24-191204-b24] The consumption of species with the lowest total mean concentrations of PAHs have a higher potential to cause carcinogenic risk, which agrees with the findings of the present study. Furthermore, the calculated TEQ values were in agreement with the values reported by Iwegbue *et al*.[@i2156-9614-9-24-191204-b41] The results of the present study are in agreement with a study of PAHs contaminants in Chrysichthys nigrodigitatus in Rivers State, Nigeria, where Patrolecco *et al.* reported TEQ values above estimated SVs.[@i2156-9614-9-24-191204-b48],[@i2156-9614-9-24-191204-b49] In addition, higher TEQ values were reported when compared to calculated SVs for PAHs in seafood (fish, crab, and bivalves) in Iran, indicating potential health effects.[@i2156-9614-9-24-191204-b5] However, these results disagreed with reports of lower estimated TEQ values than the SV in studies of PAH concentrations in fish (feral finfish) from a Hong Kong market and the common eel (Anguilla anguilla) from the River Tiber, Italy.[@i2156-9614-9-24-191204-b16],[@i2156-9614-9-24-191204-b49] Histopathological examination ----------------------------- Histopathological biomarkers are sensitive indicators of subcellular stress in organisms exposed to a range of pollutants over short and long periods of time.[@i2156-9614-9-24-191204-b50] Changes caused by toxic substances can be observed in the gills, such as an increase in pollutant blood diffusion distance as a means for protection.[@i2156-9614-9-24-191204-b50] Fusion of secondary lamellae, which is a result of hyperplasia, brings about a reduction in free gas exchange, thus affecting the general health of the fish. Hypertrophy of the primary lamellae is the enlarging or increase in size of the organ in response to a stressor in the environment. This observation is similar to a report of a high incidence of hyperplasia in Clarias gariepinus and Oreochromis niloticus reported from the Sanyati basin in Lake Kariba, Zimbabwe, as well as hyperplasia in the gills of two species of sturgeons.[@i2156-9614-9-24-191204-b50],[@i2156-9614-9-24-191204-b51] This result is an indication that the fish have been exposed to stressors. Gills are sensitive organs which are easily damaged by numerous pollutants, even at low concentrations. Gills have been reported to perform various vital functions (respiration, osmoregulation, acid-base balance). Gills have a large surface area in contact with the external environment and are particularly sensitive to chemical and physical changes of the aquatic environment, thereby being a target organ in fish for pollutants carried by water.[@i2156-9614-9-24-191204-b51],[@i2156-9614-9-24-191204-b52] Changes in the structures of these organs as well as in the vital functions performed by the gills were observed due to toxic substances present in the aquatic environment.[@i2156-9614-9-24-191204-b53] The severity of damage depends on the concentration of toxicants and the period of exposure. With prolonged exposure, these lesions could lead to fish mortality. The observed separation of muscle bundles may be due to the initial stimulus of hexachlorocyclohexane, which can induce hyperactivity and excitability in animals, leading to a release of lactic acid and subsequent muscular fatigue. The atrophy observed in the muscle bundles may be due to the exposure to various contaminants.[@i2156-9614-9-24-191204-b54] A study detected changes in muscle tissue of grass carp (Ctenopharyngodon idella) as swelling and necrosis of muscle bundles due to the effect of rice herbicides.[@i2156-9614-9-24-191204-b55] Another study documented physiological disturbances and morphological damage in the muscle tissue of freshwater fish Hoplias malabaricus collected from Ponta Lake in southern Brazil due to bioaccumulation of chlorinated pesticides and PCBs.[@i2156-9614-9-24-191204-b56] Degeneration of muscle bundles with aggregation of inflammatory cells between them and focal areas of necrosis were observed by Gingerich.[@i2156-9614-9-24-191204-b57] The findings of the present study agreed with these previous reports. The liver is the largest organ in the body and performs several important physiological functions.[@i2156-9614-9-24-191204-b58] Although every tissue has some ability to metabolize chemicals, the liver is the major organ of metabolism or transformation of toxins, making it a target organ that is highly affected by toxins in the system. Necrosis is the death of cells in a tissue or organ caused by disease or injury or as a result of exposure to harmful or toxic contaminants. The necrotic cells are shrunk, and their intercellular attachments are broken.[@i2156-9614-9-24-191204-b58] Vascular dilation may be responsible for the cellular degeneration and necrosis in the liver. When the liver is damaged, excessive blood flows into the liver, blocking the sinusoids. Oxygen deficiency as a result of gill degeneration is the most common cause of cellular degeneration in the liver (*[Figures 9a--d](#i2156-9614-9-24-191204-f09){ref-type="fig"}*).[@i2156-9614-9-24-191204-b59] The results of this study agreed with previous reports on the effects of different pollutants on fish liver.[@i2156-9614-9-24-191204-b54],[@i2156-9614-9-24-191204-b60] Conclusions =========== In the present study, low and high molecular weights PAHs were present in the sediment samples. The concentration of total PAHs in the sediment samples exceeded safe limits, suggesting that the aquatic organisms around Atlas Cove may pose serious human health and environmental risks. The high ratio of LMW PAHs as compared to HMW PAHs suggests that PAH contamination around Atlas Cove may be of natural origin. The concentration of total PAHs in biota samples indicated that PAH contamination from Atlas Cove was relatively high (with dominance of the low molecular weight PAHs). The high concentration of total PAHs present in the organisms indicated that the compounds have bioaccumulated in their tissues and organs over a period of time. The calculated TEQ values were higher than the screening values, indicating potential health effects. Histopathological examination revealed that both fish and shellfish were exposed to high concentrations of PAHs which brought about changes in morphologic structure of these organs, necrosis of the muscle bundles and cellular degeneration. This study was funded as part of employment.

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Ataxia–telangiectasia Ataxia–telangiectasia (AT or A–T), also referred to as ataxia–telangiectasia syndrome or Louis–Bar syndrome, is a rare, neurodegenerative, autosomal recessive disease causing severe disability. Ataxia refers to poor coordination and telangiectasia to small dilated blood vessels, both of which are hallmarks of the disease. A–T affects many parts of the body: It impairs certain areas of the brain including the cerebellum, causing difficulty with movement and coordination. It weakens the immune system, causing a predisposition to infection. It prevents repair of broken DNA, increasing the risk of cancer. Symptoms most often first appear in early childhood (the toddler stage) when children begin to sit or walk. Though they usually start walking at a normal age, they wobble or sway when walking, standing still or sitting. In late pre-school and early school age, they develop difficulty moving their eyes in a natural manner from one place to the next (oculomotor apraxia). They develop slurred or distorted speech, and swallowing problems. Some have an increased number of respiratory tract infections (ear infections, sinusitis, bronchitis, and pneumonia). Because not all children develop in the same manner or at the same rate, it may be some years before A–T is properly diagnosed. Most children with A–T have stable neurologic symptoms for the first 4–5 years of life, but begin to show increasing problems in early school years. A–T is caused by a defect in the ATM gene, which is involved in the recognition and repair of damaged DNA. The prevalence of A–T is estimated to be as high as 1 in 40,000 to as low as 1 in 300,000 people. Symptoms There is substantial variability in the severity of features of A–T among affected individuals, and at different ages. The following symptoms or problems are either common or important features of A–T: Ataxia (difficulty with control of movement) that is apparent early but worsens in school to pre-teen years Oculomotor apraxia (difficulty with coordination of head and eye movement when shifting gaze from one place to the next) Involuntary movements Telangiectasia (dilated blood vessels) over the white (sclera) of the eyes, making them appear bloodshot. These are not apparent in infancy and may first appear at age 5–8 years. Telangiectasia may also appear on sun-exposed areas of skin. Problems with infections, especially of the ears, sinuses and lungs Increased incidence of cancer (primarily, but not exclusively, lymphomas and leukemias) Delayed onset or incomplete pubertal development, and very early menopause Slowed rate of growth (weight and/or height) Drooling particularly in young children when they are tired or concentrating on activities Dysarthria (slurred, slow, or distorted speech sounds) Diabetes in adolescence or later Premature changes in hair and skin Many children are initially misdiagnosed as having cerebral palsy. The diagnosis of A–T may not be made until the preschool years when the neurologic symptoms of impaired gait, hand coordination, speech and eye movement appear or worsen, and the telangiectasia first appear. Because A–T is so rare, doctors may not be familiar with the symptoms, or methods of making a diagnosis. The late appearance of telangiectasia may be a barrier to the diagnosis. It may also take some time before doctors consider A–T as a possibility because of the early stability of symptoms and signs. Ataxia and other neurologic problems The first indications of A–T usually occur during the toddler years. Children start walking at a normal age, but may not improve much from their initial wobbly gait. Sometimes they have problems standing or sitting still and tend to sway backward or from side to side. In primary school years, walking becomes more difficult, and children will use doorways and walls for support. Children with A–T often appear better when running or walking quickly in comparison to when they are walking slowly or standing in one place. Around the beginning of their second decade, children with the more severe ("classic") form of A–T start using a wheelchair for long distances. During school years, children may have increasing difficulty with reading because of impaired coordination of eye movement. At the same time, other problems with fine-motor functions (writing, coloring, and using utensils to eat), and with slurring of speech (dysarthria) may arise. Most of these neurologic problems stop progressing after the age of about 12 – 15 years, though involuntary movements may start at any age and may worsen over time. These extra movements can take many forms, including small jerks of the hands and feet that look like fidgeting (chorea), slower twisting movements of the upper body (athetosis), adoption of stiff and twisted postures (dystonia), occasional uncontrolled jerks (myoclonic jerks), and various rhythmic and non-rhythmic movements with attempts at coordinated action (tremors). Telangiectasia Prominent blood vessels (telangiectasia) over the white (sclera) of the eyes usually occur by the age of 5–8 years, but sometimes appear later or not at all. The absence of telangiectasia does not exclude the diagnosis of A–T. Potentially a cosmetic problem, the ocular telangiectasia do not bleed or itch, though they are sometimes misdiagnosed as chronic conjunctivitis. It is their constant nature, not changing with time, weather or emotion, that marks them as different from other visible blood vessels. Telangiectasia can also appear on sun-exposed areas of skin, especially the face and ears. They occur in the bladder as a late complication of chemotherapy with cyclophosphamide, have been seen deep inside the brain of older people with A–T, and occasionally arise in the liver and lungs. Immune problems About two-thirds of people with A–T have abnormalities of the immune system. The most common abnormalities are low levels of one or more classes of immunoglobulins (IgG, IgA or IgE subclasses), not making antibodies in response to vaccines or infections, and having low numbers of lymphocytes (especially T-lymphocytes) in the blood. Some people have frequent infections of the upper (colds, sinus and ear infections) and lower (bronchitis and pneumonia) respiratory tract. All children with A–T should have their immune systems evaluated to detect those with severe problems that require treatment to minimize the number or severity of infections. Some people with A–T need additional immunizations (especially with pneumonia and influenza vaccines), antibiotics to provide protection (prophylaxis) from infections, and/or infusions of immunoglobulins (gamma globulin). The need for these treatments should be determined by an expert in the field of immunodeficiency or infectious diseases. Cancer People with A–T have a highly increased incidence (approximately 25% lifetime risk) of cancers, particularly lymphomas and leukemia, but other cancers can occur. When possible, treatment should avoid the use of radiation therapy and chemotherapy drugs that work in a way that is similar to radiation therapy (radiomimetic drugs), as these are particularly toxic for people with A–T. The special problems of managing cancer are sufficiently complicated that treatment should be done only in academic oncology centers and after consultation with physicians who have specific expertise in A–T. Unfortunately, there is no way to predict which individuals will develop cancer. Because leukemia and lymphomas differ from solid tumors in not progressing from solitary to metastatic stages, there is less need to diagnose them early in their appearance. Surveillance for leukemia and lymphoma is thus not helpful, other than considering cancer as a diagnostic possibility whenever possible symptoms of cancer (e.g. persistent swollen lymph glands, unexplained fever) arise. Women who are A–T carriers (who have one mutated copy of the ATM gene), have approximately a two-fold increased risk for the development of breast cancer compared to the general population. This includes all mothers of A–T children and some female relatives. Current consensus is that special screening tests are not helpful, but all women should have routine cancer surveillance. Skin A–T can cause features of early aging such as premature graying of the hair. It can also cause vitiligo (an auto-immune disease causing loss of skin pigment resulting in a blotchy “bleach-splashed” look), and warts which can be extensive and recalcitrant to treatment. A small number of people develop a chronic inflammatory skin disease (granulomas). Lung disease Chronic lung disease develops in more than 25% of people with A–T. Three major types of lung disease can develop: (1) recurrent and chronic sinopulmonary infections; (2) lung disease caused by ineffective cough, swallowing dysfunction, and impaired airway clearance; and (3) restrictive interstitial lung disease. It is common for individuals with A–T to have more than one of these lung conditions. Chronic lung disease can occur because of recurrent lung infections due to immunodeficiency. Individuals with this problem are at risk of developing bronchiectasis, a condition in which bronchial tubes are permanently damaged, resulting in recurrent lower airway infections. Gamma globulin for people with antibody deficiency and/or chronic antibiotic treatment may reduce the problems of infection. Other individuals with A–T have difficulty with taking deep breaths and may have an ineffective cough, making it difficult to clear oral and bronchial secretions. This can lead to prolonged respiratory symptoms following common viral respiratory illnesses. Techniques that allow clearance of mucus can be helpful in some individuals during respiratory illnesses. Some people will develop swallowing problems as they age, increasing their risk of aspiration pneumonia. Recurrent injury to the lungs caused by chronic infections or aspiration may cause lung fibrosis and scarring. This process may be enhanced by inadequate tissue repair in ATM-deficient cells. A small number of individuals develop interstitial lung disease. They have decreased pulmonary reserve, trouble breathing, a need for supplemental oxygen and chronic cough in the absence of lung infections. They may respond to systemic steroid treatment or other drugs to reduce inflammation. Lung function tests (spirometry) should be performed at least annually in children old enough to perform them, influenza and pneumococcal vaccines given to eligible individuals, and sinopulmonary infections treated aggressively to limit the development of chronic lung disease. Feeding, swallowing, and nutrition Feeding and swallowing can become difficult for people with A–T as they get older. Feeding refers to all aspects of eating and drinking, including getting food and liquids to the mouth; swallowing refers to ingestion or what happens after food or liquids enter the mouth. Primary goals for feeding and swallowing are safe, adequate, and enjoyable mealtimes. Involuntary movements may make feeding difficult or messy and may excessively prolong mealtimes. It may be easier to finger feed than use utensils (e.g., spoon or fork). For liquids, it is often easier to drink from a closed container with a straw than from an open cup. Caregivers may need to provide foods or liquids so that self-feeding is possible, or they may need to feed the person with A–T. In general, meals should be completed within approximately 30 minutes. Longer meals may be stressful, interfere with other daily activities, and limit the intake of necessary liquids and nutrients. If swallowing problems (dysphagia) occur, they typically present during the second decade of life. Dysphagia is common because of the neurological changes that interfere with coordination of mouth and pharynx (throat) movements that are needed for safe and efficient swallowing. Coordination problems involving the mouth may make chewing difficult and increase the duration of meals. Problems involving the pharynx may cause liquid, food, and saliva to be inhaled into the airway (aspiration). People with dysphagia may not cough when they aspirate (silent aspiration). Swallowing problems and especially swallowing problems with silent aspiration may cause lung problems due to inability to cough and clear food and liquids from the airway. Warning signs of a swallowing problem Choking or coughing when eating or drinking Poor weight gain (during ages of expected growth) or weight loss at any age Excessive drooling Mealtimes longer than 40 – 45 minutes, on a regular basis Foods or drinks previously enjoyed are now refused or difficult Chewing problems Increase in the frequency or duration of breathing or respiratory problems Increase in lung infections Eye and vision Most people develop telangiectasia (prominent blood vessels) in the membrane that covers the white part (sclera) of the eye. Vision (ability to see objects in focus) is normal. Control of eye movement is often impaired, affecting visual functions that require fast, accurate eye movements from point to point (e.g. reading). Eye misalignments (strabismus) are common, but may be treatable. There may be difficulty in coordinating eye position and shaping the lens to see objects up close. Orthopedics Many individuals with A–T develop deformities of the feet that compound the difficulty they have with walking due to impaired coordination. Early treatment may slow progression of this deformity. Bracing or surgical correction sometimes improves stability at the ankle sufficient to enable an individual to walk with support, or bear weight during assisted standing transfers from one seat to another. Severe scoliosis is relatively uncommon, but probably does occur more often than in those without A–T. Spinal fusion is only rarely indicated. Genetics A–T is caused by mutations in the ATM (ATM serine/threonine kinase or ataxia–telangiectasia mutated) gene, which was cloned in 1995. ATM is located on human chromosome 11 (11q22.3) and is made up of 69 exons spread across 150kb of genomic DNA. The mode of inheritance for A–T is autosomal recessive. Each parent is a carrier, meaning that they have one normal copy of the A–T gene (ATM) and one copy which is mutated. A–T occurs if a child inherits the mutated A–T gene from each parent, so in a family with two carrier parents, there is 1 chance in 4 that a child born to the parents will have the disorder. Prenatal diagnosis (and carrier detection) can be carried out in families if the errors (mutation) in an affected child's two ATM genes have been identified. The process of getting this done can be complicated and, as it requires time, should be arranged before conception. Looking for mutations in the ATM gene of an unrelated person (for example, the spouse of a known A–T carrier) presents significant challenges. Genes often have variant spellings (polymorphisms) which do not affect function. In a gene as large as ATM, such variant spellings are likely to occur and doctors cannot always predict whether a specific variant will or will not cause disease. Genetic counseling can help family members of an A–T patient understand what can or cannot be tested, and how the test results should be interpreted. Carriers of A–T, such as the parents of a person with A–T, have one mutated copy of the ATM gene and one normal copy. They are generally healthy, but there is an increased risk of breast cancer in women. This finding has been confirmed in a variety of different ways, and is the subject of current research. Standard surveillance (including monthly breast self-exams and mammography at the usual schedule for age) is recommended, unless additional tests are indicated because the individual has other risk factors (e.g., family history of breast cancer). Pathophysiology How does loss of the ATM protein create a multisystem disorder? A–T has been described as a genome instability syndrome, a DNA repair disorder and a DNA damage response (DDR) syndrome. ATM, the gene responsible for this multi-system disorder, encodes a protein of the same name which coordinates the cellular response to DNA double strand breaks (DSBs). Radiation therapy, chemotherapy that acts like radiation (radiomimetic drugs) and certain biochemical processes and metabolites can cause DSBs. When these breaks occur, ATM stops the cell from making new DNA (cell cycle arrest) and recruits and activates other proteins to repair the damage. Thus, ATM allows the cell to repair its DNA before the completion of cell division. If DNA damage is too severe, ATM will mediate the process of programmed cell death (apoptosis) to eliminate the cell and prevent genomic instability. Cancer and radiosensitivity In the absence of the ATM protein, cell-cycle check-point regulation and programmed cell death in response to DSBs are defective. The result is genomic instability which can lead to the development of cancers. Irradiation and radiomimetic compounds induce DSBs which are unable to be repaired appropriately when ATM is absent. Consequently, such agents can prove especially cytotoxic to A–T cells and people with A–T. Delayed pubertal development (gonadal dysgenesis) Infertility is often described as a characteristic of A–T. Whereas this is certainly the case for the mouse model of A–T, in humans it may be more accurate to characterize the reproductive abnormality as gonadal atrophy or dysgenesis characterized by delayed pubertal development. Because programmed DSBs are generated to initiate genetic recombinations involved in the production of sperm and eggs in reproductive organs (a process known as meiosis), meiotic defects and arrest can occur when ATM is not present. Immune system defects and immune-related cancers As lymphocytes develop from stem cells in the bone marrow into mature lymphocytes in the periphery, they rearrange special segments of their DNA [V(D)J recombination process]. This process requires them to make DSBs, which are difficult to repair in the absence of ATM. As a result, most people with A–T have reduced numbers of lymphocytes and some impairment of lymphocyte function (such as an impaired ability to make antibodies in response to vaccines or infections). In addition, broken pieces of DNA in chromosomes involved in the above-mentioned rearrangements have a tendency to recombine with other genes (translocation), making the cells prone to the development of cancer (lymphoma and leukemia). Progeric changes Cells from people with A–T demonstrate genomic instability, slow growth and premature senescence in culture, shortened telomeres and an ongoing, low-level stress response. These factors may contribute to the progeric (signs of early aging) changes of skin and hair sometimes observed in people with A–T. For example, DNA damage and genomic instability cause melanocyte stem cell (MSC) differentiation which produces graying. Thus, ATM may be a “stemness checkpoint” protecting against MSC differentiation and premature graying of the hair. Telangiectasia The cause of telangiectasia or dilated blood vessels in the absence of the ATM protein is not yet known. Increased alpha-fetoprotein (AFP) levels Approximately 95% of people with A–T have elevated serum AFP levels after the age of two, and measured levels of AFP appear to increase slowly over time. AFP levels are very high in the newborn, and normally descend to adult levels over the first year to 18 months. The reason for why individuals with A–T have elevated levels of AFP is not yet known. Neurodegeneration A–T is one of several DNA repair disorders which result in neurological abnormalities or degeneration. Arguably some of the most devastating symptoms of A–T are a result of progressive cerebellar degeneration, characterized by the loss of Purkinje cells and, to a lesser extent, granule cells (located exclusively in the cerebellum). The cause of this cell loss is not known, though many hypotheses have been proposed based on experiments performed both in cell culture and in the mouse model of A–T. Current hypotheses explaining the neurodegeneration associated with A–T include the following: Defective DNA damage response in neurons which can lead to Failed clearance of genomically damaged neurons during development Transcription stress and abortive transcription including topoisomerase 1 cleavage complex (TOP1cc) dependent lesions Aneuploidy Defective response to oxidative stress characterized by elevated ROS and altered cellular metabolism Mitochondrial dysfunction Defects in neuronal function: Inappropriate cell cycle re-entry of post-mitotic (mature) neurons Synaptic/vesicular dysregulation HDAC4 dysregulation Histone hypermethylation and altered epigenetics Altered protein turnover These hypotheses may not be mutually exclusive and more than one of these mechanisms may underlie neuronal cell death when there is an absence or deficiency of ATM. Further, cerebellar damage and loss of Purkinje and granule cells do not explain all of the neurologic abnormalities seen in people with A–T. The effects of ATM deficiency on the other areas of the brain outside of the cerebellum are being actively investigated. Radiation exposure People with A–T have an increased sensitivity to ionizing radiation (X-rays and gamma rays). Therefore, X-ray exposure should be limited to times when it is medically necessary, as exposing an A–T patient to ionizing radiation can damage cells in such a way that the body cannot repair them. The cells can cope normally with other forms of radiation, such as ultraviolet light, so there is no need for special precautions from sunlight exposure. Diagnosis The diagnosis of A–T is usually suspected by the combination of neurologic clinical features (ataxia, abnormal control of eye movement, and postural instability) with telangiectasia and sometimes increased infections, and confirmed by specific laboratory abnormalities (elevated alpha-fetoprotein levels, increased chromosomal breakage or cell death of white blood cells after exposure to X-rays, absence of ATM protein in white blood cells, or mutations in each of the person's ATM genes). A variety of laboratory abnormalities occur in most people with A–T, allowing for a tentative diagnosis to be made in the presence of typical clinical features. Not all abnormalities are seen in all patients. These abnormalities include: Elevated and slowly increasing alpha-fetoprotein levels in serum after 2 years of age Immunodeficiency with low levels of immunoglobulins (especially IgA, IgG subclasses, and IgE) and low number of lymphocytes in the blood Chromosomal instability (broken pieces of chromosomes) Increased sensitivity of cells to x-ray exposure (cells die or develop even more breaks and other damage to chromosomes) Cerebellar atrophy on MRI scan The diagnosis can be confirmed in the laboratory by finding an absence or deficiency of the ATM protein in cultured blood cells, an absence or deficiency of ATM function (kinase assay), or mutations in both copies of the cell's ATM gene. These more specialized tests are not always needed, but are particularly helpful if a child's symptoms are atypical. Differential diagnosis There are several other disorders with similar symptoms or laboratory features that physicians may consider when diagnosing A–T. The three most common disorders that are sometimes confused with A–T are: Cerebral palsy Friedreich's ataxia Cogan oculomotor apraxia Each of these can be distinguished from A–T by the neurologic exam and clinical history. Cerebral palsy (CP) describes a non-progressive disorder of motor function stemming from malformation or early damage to the brain. CP can manifest in many ways, given the different manner in which brain can be damaged; in common to all forms is the emergence of signs and symptoms of impairment as the child develops. However, milestones that have been accomplished and neurologic functions that have developed do not deteriorate in CP as they often do in children with A–T in the late pre-school years. Most children with ataxia caused by CP do not begin to walk at a normal age, whereas most children with A–T start to walk at a normal age even though they often "wobble" from the start. Pure ataxia is a rare manifestation of early brain damage or malformation, however, and the possibility of an occult genetic disorder of brain should be considered and sought for those in whom ataxia is the chief manif estation of CP. Children with ataxic CP will not manifest the laboratory abnormalities associated with A–T. Cogan occulomotor apraxia is a rare disorder of development. Affected children have difficulty moving their eyes only to a new visual target, so they will turn their head past the target to “drag” the eyes to the new object of interest, then turn the head back. This tendency becomes evident in late infancy and toddler years, and mostly improves with time. This contrasts to the oculomotor difficulties evident in children with A–T, which are not evident in early childhood but emerge over time. Cogan's oculomotor apraxia is generally an isolated problem, or may be associated with broader developmental delay. Friedreich ataxia (FA) is the most common genetic cause of ataxia in children. Like A–T, FA is a recessive disease, appearing in families without a history of the disorder. FA is caused by mutation in the frataxin gene, most often an expansion of a naturally occurring repetition of the three nucleotide bases GAA from the usual 5–33 repetitions of this trinucleotide sequence to greater than 65 repeats on each chromosome. Most often the ataxia appears between 10 and 15 years of age, and differs from A–T by the absence of telangiectasia and oculomotor apraxia, a normal alpha fetalprotein, and the frequent presence of scoliosis, absent tendon reflexes, and abnormal features on the EKG. Individuals with FA manifest difficulty standing in one place that is much enhanced by closure of the eyes (Romberg sign) that is not so apparent in those with A–T – even though those with A–T may have greater difficulty standing in one place with their eyes open. There are other rare disorders that can be confused with A–T, either because of similar clinical features, a similarity of some laboratory features, or both. These include: Ataxia–oculomotor apraxia type 1 (AOA1) Ataxia–oculomotor apraxia type 2 (AOA2 also known as SCAR1) Ataxia–telangiectasia like disorder (ATLD) Nijmegen breakage syndrome (NBS) Ataxia–oculomotor apraxia type 1 (AOA1) is an autosomal recessive disorder similar to A–T in manifesting increasing problems with coordination and oculomotor apraxia, often at a similar age to those having A–T. It is caused by mutation in the gene coding for the protein aprataxin. Affected individuals differ from those with A–T by the early appearance of peripheral neuropathy, early in their course manifest difficulty with initiation of gaze shifts, and the absence of ocular telangiectasia, but laboratory features are of key importance in the differentiation of the two. Individuals with AOA1 have a normal AFP, normal measures of immune function, and after 10–15 years have low serum levels of albumin. Genetic testing of the aprataxin gene can confirm the diagnosis. There is no enhanced risk for cancer. Ataxia–oculomotor apraxia type 2 (AOA2) is an autosomal recessive disorder also similar to A–T in manifesting increasing problems with coordination and peripheral neuropathy, but oculomotor apraxia is present in only half of affected individuals. Ocular telangiectasia do not develop. Laboratory abnormalities of AOA2 are like A–T, and unlike AOA1, in having an elevated serum AFP level, but like AOA1 and unlike A–T in having normal markers of immune function. Genetic testing of the senataxin gene (SETX) can confirm the diagnosis. There is no enhanced risk for cancer. Ataxia–telangiectasia like disorder (ATLD) is an extremely rare condition, caused by mutation in the hMre11 gene, that could be considered in the differential diagnosis of A–T. Patients with ATLD are very similar to those with A–T in showing a progressive cerebellar ataxia, hypersensitivity to ionizing radiation and genomic instability. Those rare individuals with ATLD who are well described differ from those with A–T by the absence of telangiectasia, normal immunoglobulin levels, a later onset, and a slower progression of the symptoms. Because of its rarity, it is not yet known whether or not ATLD carries an increased risk to develop cancer. Because those mutations of Mre11 that severely impair the MRE11 protein are incompatible with life, individuals with ATLD all have some partial function of the Mre11 protein, and hence likely all have their own levels of disease severity. Nijmegen breakage syndrome (NBS) is a rare genetic disorder that has similar chromosomal instability to that seen in people with A–T, but the problems experienced are quite different. Children with NBS have significant microcephaly, a distinct facial appearance, short stature, and moderate cognitive impairment, but do not experience any neurologic deterioration over time. Like those with A–T, children with NBS have enhanced sensitivity to radiation, disposition to lymphoma and leukemia, and some laboratory measures of impaired immune function, but do not have ocular telangiectasia or an elevated level of AFP. The proteins expressed by the hMre11 (defective in ATLD) and Nbs1 (defective in NBS) genes exist in the cell as a complex, along with a third protein expressed by the hRad50 gene. This complex, known as the MRN complex, plays an important role in DNA damage repair and signaling and is required to recruit ATM to the sites of DNA double strand breaks. Mre11 and Nbs1 are also targets for phosphorylation by the ATM kinase. Thus, the similarity of the three diseases can be explained in part by the fact that the protein products of the three genes mutated in these disorders interact in common pathways in the cell. Differentiation of these disorders is often possible with clinical features and selected laboratory tests. In cases where the distinction is unclear, clinical laboratories can identify genetic abnormalities of ATM, aprataxin and senataxin, and specialty centers can identify abnormality of the proteins of potentially responsible genes, such as ATM, MRE11, nibrin, TDP1, aprataxin and senataxin as well as other proteins important to ATM function such as ATR, DNA-PK, and RAD50. Management Ataxia and other neurologic problems There is no treatment known to slow or stop the progression of the neurologic problems. Treatment of A–T is symptomatic and supportive. Physical, occupational and speech therapies and exercise may help maintain function but will not slow the course of neurodegeneration. Therapeutic exercises should not be used to the point of fatigue and should not interfere with activities of daily life. Certain anti-Parkinson and anti-epileptic drugs may be useful in the management of symptoms, but should be prescribed in consultation with a neurologist. Immune problems All individuals with A–T should have at least one comprehensive immunologic evaluation that measures the number and type of lymphocytes in the blood (T-lymphocytes and B-lymphocytes), the levels of serum immunoglobulins (IgG, IgA, and IgM) and antibody responses to T-dependent (e.g., tetanus, Hemophilus influenzae b) and T-independent (23-valent pneumococcal polysaccharide) vaccines. For the most part, the pattern of immunodeficiency seen in an A–T patient early in life (by age five) will be the same pattern seen throughout the lifetime of that individual. Therefore, the tests need not be repeated unless that individual develops more problems with infection. Problems with immunity sometimes can be overcome by immunization. Vaccines against common bacterial respiratory pathogens such as Hemophilus influenzae, pneumococci and influenza virus (the “flu”) are commercially available and often help to boost antibody responses, even in individuals with low immunoglobulin levels. If the vaccines do not work and the patient continues to have problems with infections, gamma globulin therapy (IV or subcutaneous infusions of antibodies collected from normal individuals) may be of benefit. A small number of people with A–T develop an abnormality in which one or more types of immunoglobulin are increased far beyond the normal range. In a few cases, the immunoglobulin levels can be increased so much that the blood becomes thick and does not flow properly. Therapy for this problem must be tailored to the specific abnormality found and its severity. If an individual patient's susceptibility to infection increases, it is important to reassess immune function in case deterioration has occurred and a new therapy is indicated. If infections are occurring in the lung, it is also important to investigate the possibility of dysfunctional swallow with aspiration into the lungs (see above sections under Symptoms: Lung Disease and Symptoms: Feeding, Swallowing and Nutrition.) Most people with A–T have low lymphocyte counts in the blood. This problem seems to be relatively stable with age, but a rare number of people do have progressively decreasing lymphocyte counts as they get older. In the general population, very low lymphocyte counts are associated with an increased risk for infection. Such individuals develop complications from live viral vaccines (measles, mumps, rubella and chickenpox), chronic or severe viral infections, yeast infections of the skin and vagina, and opportunistic infections (such as pneumocystis pneumonia). Although lymphocyte counts are often as low in people with A–T, they seldom have problems with opportunistic infections. (The one exception to that rule is that problems with chronic or recurrent warts are common.) The number and function of T-lymphocytes should be re-evaluated if a person with A–T is treated with corticosteroid drugs such as prednisone for longer than a few weeks or is treated with chemotherapy for cancer. If lymphocyte counts are low in people taking those types of drugs, the use of prophylactic antibiotics is recommended to prevent opportunistic infections. If the tests show significant abnormalities of the immune system, a specialist in immunodeficiency or infectious diseases will be able to discuss various treatment options. Absence of immunoglobulin or antibody responses to vaccine can be treated with replacement gamma globulin infusions, or can be managed with prophylactic antibiotics and minimized exposure to infection. If antibody function is normal, all routine childhood immunizations including live viral vaccines (measles, mumps, rubella and varicella) should be given. In addition, several “special” vaccines (that is, licensed but not routine for otherwise healthy children and young adults) should be given to decrease the risk that an A–T patient will develop lung infections. The patient and all household members should receive the influenza (flu) vaccine every fall. People with A–T who are less than two years old should receive three (3) doses of a pneumococcal conjugate vaccine (Prevnar) given at two month intervals. People older than two years who have not previously been immunized with Prevnar should receive two (2) doses of Prevnar. At least 6 months after the last Prevnar has been given and after the child is at least two years old, the 23-valent pneumococcal vaccine should be administered. Immunization with the 23-valent pneumococcal vaccine should be repeated approximately every five years after the first dose. In people with A–T who have low levels of IgA, further testing should be performed to determine whether the IgA level is low or completely absent. If absent, there is a slightly increased risk of a transfusion reaction. “Medical Alert” bracelets are not necessary, but the family and primary physician should be aware that if there is elective surgery requiring red cell transfusion, the cells should be washed to decrease the risk of an allergic reaction. People with A–T also have an increased risk of developing autoimmune or chronic inflammatory diseases. This risk is probably a secondary effect of their immunodeficiency and not a direct effect of the lack of ATM protein. The most common examples of such disorders in A–T include immune thrombocytopenia (ITP), several forms of arthritis, and vitiligo. Lung disease Recurrent sinus and lung infections can lead to the development of chronic lung disease. Such infections should be treated with appropriate antibiotics to prevent and limit lung injury. Administration of antibiotics should be considered when children and adults have prolonged respiratory symptoms (greater than 7 days), even following what was presumed to have been a viral infection. To help prevent respiratory illnesses from common respiratory pathogens, annual influenza vaccinations should be given and pneumococcal vaccines should be administered when appropriate. Antibiotic treatment should also be considered in children with chronic coughs that are productive of mucous, those who do not respond to aggressive pulmonary clearance techniques and in children with muco-purulent secretions from the sinuses or chest. A wet cough can also be associated with chronic aspiration which should be ruled out through proper diagnostic studies, however aspiration and respiratory infections are not necessarily exclusive of each other. In children and adults with bronchiectasis, chronic antibiotic therapy should be considered to slow chronic lung disease progression. Culturing of the sinuses may be needed to direct antibiotic therapy. This can be done by an Ear Nose and Throat (ENT) specialist. In addition, diagnostic bronchoscopy may be necessary in people who have recurrent pneumonias, especially those who do not respond or respond incompletely to a course of antibiotics. Clearance of bronchial secretions is essential for good pulmonary health and can help limit injury from acute and chronic lung infections. Children and adults with increased bronchial secretions can benefit from routine chest therapy using the manual method, an a cappella device or a chest physiotherapy vest. Chest physiotherapy can help bring up mucous from the lower bronchial tree, however an adequate cough is needed to remove secretions. In people who have decreased lung reserve and a weak cough, use of an insufflator-exsufflator (cough-assist) device may be useful as a maintenance therapy or during acute respiratory illnesses to help remove bronchial secretions from the upper airways. Evaluation by a Pulmonology specialist however, should first be done to properly assess patient suitability. Children and adults with chronic dry cough, increased work of breathing (fast respiratory rate, shortness of breath at rest or with activities) and absence of an infectious process to explain respiratory symptoms should be evaluated for interstitial lung disease or another intrapulmonary process. Evaluation by a Pulmonologist and a CT scan of the chest should be considered in individuals with symptoms of interstitial lung disease or to rule other non-infectious pulmonary processes. People diagnosed with interstitial lung disease may benefit from systemic steroids. Feeding, swallowing and nutrition Oral intake may be aided by teaching persons with A–T how to drink, chew and swallow more safely. The propriety of treatments for swallowing problems should be determined following evaluation by an expert in the field of speech-language pathology. Dieticians may help treat nutrition problems by recommending dietary modifications, including high calorie foods or food supplements. A feeding (gastrostomy) tube is recommended when any of the following occur: A child cannot eat enough to grow or a person of any age cannot eat enough to maintain weight; Aspiration is problematic; Mealtimes are stressful or too long, interfering with other activities. Feeding tubes can decrease the risk of aspiration by enabling persons to avoid liquids or foods that are difficult to swallow and provide adequate calories without the stress and time commitment of prolonged meals. Gastrostomy tubes do not prevent people from eating by mouth. Once a tube is in place, the general goal should be to maintain weight at the 10–25th percentile. Education and socialization Most children with A–T have difficulty in school because of a delay in response time to visual, verbal or other cues, slurred and quiet speech (dysarthria), abnormalities of eye control (oculomotor apraxia), and impaired fine motor control. Despite these problems, children with A–T often enjoy school if proper accommodations to their disability can be made. The decision about the need for special education classes or extra help in regular classes is highly influenced by the local resources available. Decisions about proper educational placement should be revisited as often as circumstances warrant. Despite their many neurologic impairments, most individuals with A–T are very socially aware and socially skilled, and thus benefit from sustained peer relationships developed at school. Some individuals are able to function quite well despite their disabilities and a few have graduated from community colleges. Many of the problems encountered will benefit from special attention, as problems are often related more to “input and output” issues than to intellectual impairment. Problems with eye movement control make it difficult for people with A–T to read, yet most fully understand the meaning and nuances of text that is read to them. Delays in speech initiation and lack of facial expression make it seem that they do not know the answers to questions. Reduction of the skilled effort needed to answer questions, and an increase of the time available to respond, is often rewarded by real accomplishment. It is important to recognize that intellectual disability is not regularly a part of the clinical picture of A–T although school performance may be suboptimal because of the many difficulties in reading, writing, and speech. Children with A–T are often very conscious of their appearance, and strive to appear normal to their peers and teachers. Life within the ataxic body can be tiring. The enhanced effort needed to maintain appearances and increased energy expended in abnormal tone and extra movements all contribute to physical and mental fatigue. As a consequence, for some a shortened school day yields real benefits. General recommendations All children with A–T need special attention to the barriers they experience in school. In the United States, this takes the form of a formal IEP (Individualized Education Program). Children with A–T tend to be excellent problem solvers. Their involvement in how to best perform tasks should be encouraged. Speech-language pathologists may facilitate communication skills that enable persons with A–T to get their messages across (using key words vs. complete sentences) and teach strategies to decrease frustration associated with the increase time needed to respond to questions (e.g., holding up a hand and informing others about the need to allow more time for responses). Rarely helpful are traditional speech therapies that focus on the production of specific sounds and strengthening of the lip and tongue muscles. Classroom aides may be appropriate, especially to help with scribing, transportation through the school, mealtimes and toileting. The impact of an aide on peer relationships should be monitored carefully. Physical therapy is useful to maintain strength and general cardiovascular health. Horseback therapy and exercises in a swimming pool are often well tolerated and fun for people with A–T. However, no amount of practice will slow the cerebellar degeneration or improve neurologic function. Exercise to the point of exhaustion should be avoided. Hearing is normal throughout life. Books on tape may be a useful adjunct to traditional school materials. Early use of computers (preschool) with word completion software should be encouraged. Practicing coordination (e.g. balance beam or cursive writing exercises) is not helpful. Occupational therapy is helpful for managing daily living skills. Allow rest time, shortened days, reduced class schedule, reduced homework, modified tests as necessary. Like all children, those with A–T need to have goals to experience the satisfaction of making progress. Social interactions with peers are important, and should be taken into consideration for class placement. For everyone long-term peer relationships can be the most rewarding part of life; for those with A–T establishing these connections in school years can be helpful. Treatment No curative medication has been approved for the treatment of inherited cerebellar ataxias, including Ataxia-Telangiectasia. The treatment of A-T remains based in medical management (of immunodeficiencies and sinopulmonary infections, neurologic dysfunction, and malignancy) and neurorehabilitation (physical, occupational, and speech/swallowing therapy; adaptive equipment; and nutritional counseling). N-Acetyl-Leucine N-Acetyl-Leucine is an orally administered, modified amino acid that is being developed as a novel treatment for multiple rare and common neurological disorders by IntraBio Inc (Oxford, United Kingdom). N-Acetyl-Leucine has been granted multiple orphan drug designations from the U.S. Food & Drug Administration (FDA)and the European Medicines Agency (EMA)for the treatment of various genetic diseases, including Ataxia-Telangiectasia. N-Acetyl-Leucine has also been granted Orphan Drug Designations in the US and EU for related inherited cerebellar ataxias, such as Spinocerebellar Ataxias. U.S. Food & Drug Administration (FDA) and the European Medicines Agency (EMA). Published case series studies have demonstrated the positive clinical benefit of treatment with N-Acetyl-Leucine various inherited cerebellar ataxias. Additional compassionate use studies in patients with Ataxia Telangiectasia have shown the symptomatic, and disease-modifying potential of the treatment. These studies further demonstrated that the treatment is well tolerated, with a good safety profile. A multinational clinical trial investigating N-Acetyl-L-Leucine for the treatment Ataxia-Telangiectasia began in 2019. IntraBio is also conducting two parallel clinical trials with N-Acetyl-L-Leucine for the treatment Niemann-Pick disease type C and GM2 Gangliosidosis (Tay-Sachs and Sandhoff Disease) Future opportunities to develop N-Acetyl-Leucine include Lewy Body Dementia, Amyotrophic lateral sclerosis, Restless Leg Syndrome, Multiple Sclerosis, and Migraine. Prognosis The life expectancy of people with A–T is highly variable. The average is approximately 25 years, but continues to improve with advances in care. The two most common causes of death are chronic lung disease (about one-third of cases) and cancer (about one-third of cases). Epidemiology Individuals of all races and ethnicities are affected equally. The incidence worldwide is estimated to be between 1 in 40,000 and 1 in 100,000 people. Research directions An open-label Phase II clinical trial studying the use of red blood cells (erythrocytes) loaded with dexamethasone sodium phosphate found that this treatment improved symptoms and appeared to be well tolerated. This treatment uses a unique delivery system for medication by using the patient's own red blood cells as the delivery vehicle for the drug. Given the other immunologic deficits present in individuals with A–T, there remains a need to evaluate the therapeutic potential of steroids further, particularly with respect to the duration of any benefit and its long-term safety. References External links About A–T from the NINDS Orphanet for A–T GeneReviews for ataxia–telangiectasia Replication-Independent Double-Strand Breaks (DSBs) Discusses importance of the ATM kinase Category:Chromosome instability syndromes Category:Genodermatoses Category:Systemic atrophies primarily affecting the central nervous system Category:Neurodegenerative disorders Category:IUIS-PID table 3 immunodeficiencies Category:DNA replication and repair-deficiency disorders Category:Syndromes affecting the nervous system Category:Syndromes with tumors

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Ripples in spacetime: Science's 2016 Breakthrough of the Year The discovery of ripples in spacetime—gravitational waves—shook the scientific world this year. It fulfilled a prediction made 100 years ago by Albert Einstein and capped a 40-year quest to spot the infinitesimal ripples. But instead of the end of the story, scientists see the discovery as the birth of a new field: gravitational wave astronomy. In 1915, Einstein explained that gravity arises because massive bodies warp space and time, or spacetime, causing free- falling objects to follow curved paths such as the arc of a thrown ball or the elliptical orbit of a planet around its sun. Einstein then calculated that a barbell-shaped distribution of mass whirling end-to-end like a baton should radiate ripples in spacetime that zip along at light speed—gravitational waves. On 11 February, physicists working with the Laser Interferometer Gravitational-Wave Observatory (LIGO)—twin instruments in Hanford, Washington, and Livingston, Louisiana—announced that they had seen just what Einstein predicted: a burst of waves created as two black holes spiraled into each other 1.3 billion light- years away. The triumph was hard earned. Einstein himself vacillated for decades over whether gravitational waves should exist. Even if they did, the only source Einstein could imagine, two orbiting stars, would produce waves too feeble to detect. By the late 1960s, however, astrophysicists knew of much denser concentrations of mass. They had spotted neutron stars and dreamed up black holes, the ultraintense gravitational fields left behind when massive stars collapse to nothing. Spiraling together, such things could, in theory, produce observable waves. In 1972, Rainer Weiss, a physicist at the Massachusetts Institute of Technology in Cambridge, set out a scheme to detect them with L-shaped optical instruments called interferometers, sowing the seed for LIGO. People’s choice Visitors to Science’s website were offered the chance to vote on a list of candidates for Breakthrough of the Year while Science editors and writers were finalizing their choices. A first round of voting narrowed the top candidates to five, and a second round, in which some 225,000 votes were cast, determined the final People’s Choice. In the end, a breakthrough in culture techniques that enabled researchers to keep human embryos developing in the lab for almost 2 weeks edged out Science’s top choice, the detection of gravitational waves. The full results: Human embryo culture 43% Gravitational waves 32% Portable DNA sequencers 13% AI beats Go champ 7% Worn-out cells and aging 5% The discovery of ripples in spacetime—gravitational waves—shook the scientific world this year. It fulfilled a prediction made 100 years ago by Albert Einstein and capped a 40-year quest to spot the infinitesimal ripples. But instead of the end of the story, scientists see the discovery as the birth of a new field: gravitational wave astronomy. In 1915, Einstein explained that gravity arises because massive bodies warp space and time, or spacetime, causing free- falling objects to follow curved paths such as the arc of a thrown ball or the elliptical orbit of a planet around its sun. Einstein then calculated that a barbell-shaped distribution of mass whirling end-to-end like a baton should radiate ripples in spacetime that zip along at light speed—gravitational waves. On 11 February, physicists working with the Laser Interferometer Gravitational-Wave Observatory (LIGO)—twin instruments in Hanford, Washington, and Livingston, Louisiana—announced that they had seen just what Einstein predicted: a burst of waves created as two black holes spiraled into each other 1.3 billion light- years away. The triumph was hard earned. Einstein himself vacillated for decades over whether gravitational waves should exist. Even if they did, the only source Einstein could imagine, two orbiting stars, would produce waves too feeble to detect. By the late 1960s, however, astrophysicists knew of much denser concentrations of mass. They had spotted neutron stars and dreamed up black holes, the ultraintense gravitational fields left behind when massive stars collapse to nothing. Spiraling together, such things could, in theory, produce observable waves. In 1972, Rainer Weiss, a physicist at the Massachusetts Institute of Technology in Cambridge, set out a scheme to detect them with L-shaped optical instruments called interferometers, sowing the seed for LIGO. Each LIGO interferometer has two 4- kilometer-long arms with mirrors at either end, housed in a giant vacuum chamber. By bouncing laser light between the mirrors, physicists can compare the arms’ lengths to within 1/10,000 the width of a proton. A passing gravitational wave would generally stretch the arms by different amounts, and that’s what the LIGO team spotted. The tight fit between that first signal and computer modeling validated Einstein’s theory of gravity, known as general relativity, as never before. Now, physicists are eagerly anticipating what may come next, because gravitational waves promise an entirely new way to peer into the cosmos. First, physicists hope to spot many more events. LIGO already has detected a second black hole merger and a third, weaker signal. The interferometers resumed taking data last month, and if they can reach their design sensitivity, they may eventually see a black hole merger on average once a day. Other instruments will soon join the hunt. The upgraded VIRGO detector in Italy should turn on early next year. Physicists in Japan are building a detector called the Kamioka Gravitational Wave Detector, and LIGO physicists plan to add a detector in India in the early 2020s. Three or more detectors together should be able to pinpoint a source in the sky by triangulation. That could help telescopes home in on the same event, and perhaps detect other signals from it. For example, if gravitational wave detectors sense the merger of two neutron stars and telescopes pick up light or x-rays from it, the signals together might offer clues about the exotic matter in neutron stars. The detectors might even test wilder ideas about black holes. Quantum theory suggests a black hole might contain a hidden “firewall” that would obliterate anything that falls in. If so, merging black holes should produce gravitational wave echoes, some theorists predict. Others speculate that a spinning black hole could generate a cloud of hypothetical particles called axions, which could generate gravitational waves by annihilating one another en masse. Meanwhile, some astronomers are trying to detect gravitational waves in a different way. Within the hearts of large galaxies lurk supermassive black holes weighing hundreds of millions or billions of solar masses. When two such monsters merge, they radiate hugely powerful waves with wavelengths light-years long—thousands of times longer than instruments like LIGO can detect. To spot those waves, astronomers are turning to stellar timepieces called millisecond pulsars. Pulsars—spinning neutron stars—emit incredibly regular pulses of radio waves. As long-wavelength gravitational waves buffet Earth, they should push the planet toward some pulsars and away from others. That motion would, in turn, shorten or stretch the time between pulses from pulsars in different directions, in an effect akin to the Doppler shift. The resulting variations and correlations among pulsars’ timing should reveal the cacophony of long-wavelength gravitational waves, and the spectrum of longer and shorter waves would help physicists trace the rate at which galaxies formed and merged throughout cosmic history. Teams in the United States, Europe, and Australia hope to see a signal within 2 or 3 years— although the U.S. effort is threatened by plans at the National Science Foundation to defund the two radio telescopes it uses.

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Artificial Intelligence has already become an essential part of our lives. Several sectors like Politics, Media, and Engineering, etc. are capitalizing all of the capacity of Artificial Intelligence. Hence, we are consuming the services of AI in known or unknown ways. Related Articles Humans created Artificial Intelligence for us to imagine a healthy, secure, connected and creative future ahead. Mechanical Engineering plays a catalyst in the above process of Imagination. In today’s era, education courses are helping us to create people who can bring the distance of Humans and Machines closer. Which can help create new products, systems, and avenues. Let us start from the basic, What is Artificial Intelligence? Artificial Intelligence, well-spoken as A.I is a unit of computer science that works towards creating and building smart appliances/machines which are capable of doing similar or more amount of work than human tendency. Work that requires human intelligence but can be done by Computer Science. A. I simulate and emulate a human’s behavioural pattern through machines. Mechanical Engineering? Mechanical Engineering is a branch of engineering dealing with Design, construction and machines. Within this, a significant area which is related to Artificial Intelligence is Mechanical Design. Mechanical Design comes to be a sub-set for Mechanical Engineering. In Mechanical Engineering Design, we can see the way toward concocting a part, framework or stream to meet desired/needed need. Here, we can see the amalgamation of Science and mathematics. Mechanical Design is a process to design the required component, system, or process, which is necessary to meet the final result. Mechanical Engineering – Mechanical Design and its relation with A.I is majorly used by a Product Design Company. Artificial Intelligence and Mechanical Engineering. The sector of Mechanical Engineering is the primary consumer of Artificial Intelligence as a technology. It is more than any other industry; it is consumed the most in Mechanical designs or engineering works. Sections of Mechanical Engineering like Robotics, Automation, or sensor technology, uses Artificial Intelligence as a technology. So it is easy to say that Mechanical Engineering disseminates the application and use of AI in the eco-system. Benefits of AI for Mechanical Engineering There are different areas where AI impacts the Mechanical Engineering process. The idea behind the work of AI remains the same. It performs activities without humans yet with increased tendency as compared to humans. It is prioritizing the automated part of work, where we feed the computer with data, and as per the command, the machine/process continues its function. We can feel the impact of AI in different areas, such as: Manufacturing Many processes in the manufacturing industry require Mechanical Engineering to be done with components, products, processes, etc. Artificial Intelligence is currently used in similar processes of Mechanical Engineering. Whether in Components, Products, or Processes. It is making sure about its presence being felt. There are many other processes and technologies which are becoming easy – fast and efficient with the help of Artificial Intelligence. Machine’s which can do more work than human tendency and that too with least effort of humans into it is the main goal here. When the above objective is achieved or worked upon, it will send serious implications to different areas of the sector. (And at some places, connections have already started affecting the scenarios) That’s what AI is impacting in the current era for the manufacturing industry. People of the sector are also scared off them losing the jobs. Mechanical Design Whenever we start the process of building a component/product/flow, the first step of it would be of Mechanical Design. Different sectors of services are provided through mechanical Design. To list the few as; Product Design, Machine Design, Mechanical Component Design, Tooling and Fixture Development, Mold Design, Casting Design. All are coming under the umbrella for Mechanical Design Services. A. I. can majorly impact Product Design Services when it comes to designing the concept, examining the product, and also during the manufacturing of the product. Big Data Storage and Usage through IT. Data has proved its presence everywhere. Even the processes and function of Mechanical engineering requires the usage and storage of Data. When it comes to mechanical engineering, the primary area where Data is needed the most is machine learning. Yet another segment of mechanical engineering. Machine learning has changed the perception of the potential of mechanical engineering. It provides better efficiency/flexibility and quality of systems with the help of data, resulting in the improvement of processes and systems in mechanical engineering. It is one of the critical drivers of development for mechanical engineering. Coming back to the discussion of AI’s impact, Artificial Intelligence has a significant role in the increasing trend of Machine Learning. A. I has its comfort zone when it comes to relying on Huge Data and Large Algorithmic learnings. Machine learning, as discussed earlier, is dependent mostly on the constant generation of data and its analysis. A. I learn through those large sets of data and various commands that engineers might have to give in the first place. There are a few other ways where Artificial Intelligence does help during the process of Mechanical Engineering. Such as, Stress Estimation of 3D Structures: Estimating the amount of stress while designing and manufacturing 3D structures. Material Evaluation for different Services: Evaluating materials, its strength – durability – quality and helping in a more exceptional manufacturing process. Structure Generation: While Generating a Structure, AI can help through its algorithms and data storage. It is making the process efficient and transparent. As we discussed, the Impact of AI on mechanical engineering. There are both sides available to Artificial Intelligence: Good and Bad. The Good Ones A. I. can create a negligible amount of error, required that the programming is done in the best possible way. Compared to A. I, Humans have a probability of creating more errors in the work. Compared to Human Speed, it is much faster w.r.t. Work. A. I. lessens the amount of risk attached to the functioning and decision-making process. Through its algorithms and data, it is created to choose only the best possible result. The Bad Ones AI reduces the risk attached to work through its attributes of data and algorithms. But the same process eradicates the Human element attached to the entire process. Resulting in an impact on Moral of the employees. AI lacks creativity. The judgment process of AI is not dynamic, i.e., according to situations. It might not give the best possible output in a condition of Natural Calamity, Disaster, or any on-ground damage. Conclusion Artificial Intelligence isn’t a long listed dream anymore. More and more industries are taking advantage of it and providing some fantastic results that can help human eco-system. Yes, AI might affect an industry’s HR by eradicating the least essential employee. Yes, it might kill the human element attached to the process. Yet, against all of it, it is helping our generation to imagine an entirely new world by impacting the different fields. It is a Superpower. If it is not used with maturity and responsibility, it has all the possibility to backfire us. Remember the Avengers? The post Artificial Intelligence and its Alliance with Mechanical Engineering appeared first on Blog Tesla Outsourcing Services.

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Students work on their own on the Think About It problem. This is a quick problem for students to complete. Students fill in the ratio table. As a class, we discuss why a tape diagram could not be the visual model for this problem. I frame the lesson by telling students that, in this lesson, they will learn a third model that can be used with ratios. Specifically, double number lines are used with part to part rations that have different units. Resources (1) Resources In the Intro to New Material section, students learn to create the double number line model. I guide students to create the double number line for the first example problem. We need to use two number lines because we're representing quantities with different units. I tell students that it would not make sense to model minutes and miles on the same number line. Using these steps, we fill in the notes in this section: Steps for Drawing Double Number lines: Draw two straight parallel lines and label with units and arrow as the end. Draw a tick mark through both lines and label with given ratio. Start with 0 and 0 on each number line. Label the units of each number line. Use skip counting to find equivalent ratios and plot them equidistant from each other. Draw tick marks and label. Stop when the unknown term has been reached. Circle and answer with units. I then guide students through completing the next example in this set. The student sample, from the Independent Practice problem set, shows what student-created double number lines should look like. Resources (2) Resources Students work in pairs for the Partner Practice. As students work, I circulate around the room. I am looking for: Are students correctly labeling the double number lines? Are students correctly drawing the double number line? Equal spacing, numbers that correspond to A are along the same line and B along another line? Are students correctly skip counting to solve the problem. Are students showing clear, logical work? Are students providing an answer to the specific question? Are students checking for the reasonableness of their answer? I'm asking students: What does the ratio mean in this problem? What is the value of each part? How do you know? What is the question asking you to find? How did you know to use a double number line? How did you find the values for the intervals on the double number line? How do you know when to stop skip counting? After 10 minutes of partner work time, the class comes back together. I pull a popsicle stick to cold call on a student. I display one of the double number lines that this student has completed. I cold call another student and ask if the work shown contains a double number line that's constructed correctly. I cold call a third student and ask how the original student knew when to stop the double number line. We discuss problem 2 from this set after work time. I want students using double number lines when the units are different. For problem 2, both parts are measured in rows. Students can use a tape diagram (or ratio table) to solve. It's very likely that students will have used a double number line to represent this problem. Numerically, they will come to the right answer. The conversation after work time will reinforce for students that they should use a double number line for part to part relationships with different units. Otherwise, we'd be able to model the quantities on one number line, if they have the same unit. I then guide students to discuss problem number 4, which involves a total. We discuss the model that would work best here. There will be students who used a double number line, labeling tulips and daisies for each respective number line. They'll have run into the problem of not having a total in the model to work with. Students then independently complete the check for understanding at the end of this section. After 3 minutes of work time, I have students clap out their answer choice for this problem. Resources (1) Resources After 15 minutes of work time, I have students turn and talk with their partners about their responses from problem number 4 in this set. I want students to talk about multiple ways to make sense of this problem. We then discuss problem 7 as a class. I want students to articulate how the differences in the pizza problems led students to model the problems in different ways. Resources (1) Resources I ask students to work with their partners to summarize when a double number line would be the most appropriate visual model. I ask 2-3 pairs to share out their thoughts, and we synthesize the responses into one common understanding: double number lines are used for part to part ratio problems with different units. Resources S Laguda: I think this is a wonderful start in introducing the lesson. Thank you for sharing this. It allows students to work on drawing the double number line, equidistance, etc. I will be using this tomorrow. | 3 months ago | Reply

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Annual fish as a genetic model for aging. Advancement in the genetics of aging and identification of longevity genes has been largely due to the model organisms such as Caenorhabditis elegans and Drosophila melanogaster. However, knowledge gained from these invertebrates will not be able to identify vertebrate-specific longevity genes. The mouse has a relatively long life span of about 3 years, which limits its utility for screening of longevity genes. Fish have been used in aging studies. However, systematic comparison of survivorship curves for fish is lacking. In this study, we compared the survivorship curves of zebrafish and 2 different annual fish, namely, Cynolebias nigripinnis and Nothobranchius rachovii. These studies established that Nothobranchius rachovii has the shortest life span (8.5 months, at which time 10% of population remains). We also established that it is possible to breed Nothobranchius rachovii under laboratory conditions, and showed that their embryos can be stored for several months and hatched at any time by adding water. In addition, we have isolated 31 cDNA markers out of 71 attempted amplifications based on corresponding homologous genomic sequences in zebrafish and Fugu available from public databases, suggesting that approximately 40% of the genes from Nothobranchius rachovii could be easily isolated. Thus, the ability to be bred under laboratory conditions and the availability of cDNA markers for mapping, along with the major advantage of a relatively short life span, make Nothobranchius rachovii an attractive vertebrate genetic model for aging over other available vertebrate models.

3.203125

3

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With the slow march of the stars to the west each evening and each season, the starry patterns form a celestial calendar. In the northern hemisphere, winter begins on December 21 at 4:44 a.m. CST. At this time the sun’s celestial coordinates are 18 hours of right ascension and -23.5 degrees declination. The sun passes overhead at Tropic of Capricorn, 23.5 degrees south of the equator. On ancient star maps, the sun appeared in front of the stars of Capricornus. Over time the earth has pivoted from the sun’s and moon’s gravitational forces so that the astronomical solstice point appears in front of Sagittarius. See more about this below. The group of stars that signal the beginning of winter is the informal group known as the Winter Triangle that are made of Sirius, Procyon and Sirius. This giant sidereal shape appears complete in the southeastern sky by 9:30 p.m. CST in late December. Sirius, the brightest star in the night sky, is distinctly blue-white through binoculars. It may twinkle vividly when viewed near the horizon on a clear, cold night from heat rising from your terrestrial surroundings. Procyon — known as “Before the Dog” because it rises a little before Sirius, the Dog Star — appears farther north along the eastern horizon. Procyon is not as blue as Sirius. The third corner of the triangle is Betelgeuse, the reddish star at the shoulder or armpit of Orion. Its colors are distinct through binoculars and a small telescope as well. The change of seasons brings us a procession of new celestial signs. The Winter Triangle and other bright stars in the eastern sky tell us that Winter is here. The constellations are represented by multiple definitions. The familiar stick figures made by connecting the stars is the most common fashion. Another way is to divide the sky into patches like those on a quilt, although each is not equal in size. The chart above shows the sun at solstice noon. (The green line represents the sun’s apparent annual path on the sky that is caused by the earth’s revolution. The moon and planets appear to move closely to that line, not on it but within a few degrees. The red line at the top is the celestial equator; it is directly above our planet’s equator in the sky. The vertical white line is the meridian, an imaginary line that starts at the southern horizon, goes through the overhead – zenith — generally through the North Star — and to the northern horizon.) The meridian divides the rising stars from the setting stars. It marks the highest point a celestial object can reach during that day. For the sun, it is noon. When the sun is east of the meridian, that’s morning; we use the letters “a.m.” (ante meridiem)to designate that the sun is before the meridian. When it is west of the meridian, that’s afternoon and we use the letters “p.m.” (post meridiem) to designate that the sun has past the meridian. For me in that moment of time when the sun is south, it is neither 12 a.m. nor 12 p.m. It is Noon. So next time you meet somebody for lunch, great them with a “Good Noon!” Earlier this year the Internet’s heart fluttered when a NASA expert stated there were 13 “signs” (for example see) in the zodiac. This is not news. The zodiac is the constellations that form the background for the real and apparent movement of the sun, moon and planets. Notice on the chart above that the ecliptic, the plane of our solar system, goes through Ophiuchus, the Snake Handler, which may have been a predecessor to the modern physician. The time that the sun spends in front of the stars of Ophiuchus is longer than the time in Scorpius. This is the constellation that made the Internet’s heart skip a beat. And there are occasions when the moon moves through part of Orion. So there are 14 constellations that form the zodiac. It’s not news, though. Have a happy holiday season. For me, it’s Christmas, so I wish you “A Merry Christmas” and a “Joyous New Year.” For my readers south of the equator, it’s summer. Have a great time at the beach!

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4

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Increased processor demands continue to drive advances in central processing units (CPUs), bandwidth and associated memory devices. A CPU typically includes a die, or microchips, which contain multiple processing units, communications hardware, and a local networking or communications bus. The core logic chipsets (cores) are the components that make up the processor die. The cores comprise the central processing logic of a computing system. A system's core logic typically includes a controller for handling memory functions, a cache for storing instructions, the logic for bus interfaces, and the functions of data paths. A single die can contain hundreds of processor cores. In increasing the number of cores, computer performance also increases, as does the need for more memory. For efficiency considerations, the memory-to-processor core ratio must stay relatively constant. That is, as more processors are added, memory must be proportionally added. The need for higher memory to processor-core ratios is further driven by advances in virtualization. Virtualization makes it possible to run multiple operating systems and multiple applications on the same computer at the same time, increasing the utilization and flexibility of hardware. In one respect, virtualization allows the transformation of hardware into software, including the CPU, RAM, hard disk and network controller, to create a fully functional virtual machine that can run its own operating system and applications just like a physical computer. Virtualization is advantageous because it allows for server consolidation and increased processor accessibility. And thus, virtualization is driving the need for even higher memory to processor-core ratios, and higher memory capacity on servers. The increased processing afforded by virtualization requires the addition of memory to maintain the required ratio. For speed considerations, the preferred way to add memory is to attach main memory directly to the CPU. Performance is increased with data being stored directly in main memory, as opposed to slower, remote memory, e.g., memory on a disk. However, attaching memory directly to the CPU typically imposes a limitation on the total amount of available memory. Attached memory may be inadequate for applications requiring larger memory capacities. Caching is commonly used to speed memory processes. A cache memory is smaller, faster and typically more expensive than main memory. When a CPU requests data that resides in main memory, the processing system transmits the requested data to the processor and also may store the data in a cache memory. When the processor issues a subsequent request for the same data, the processing system first checks cache memory. If requested data resides in the cache, the system gets a cache “hit” and delivers the data to the processor from the cache. If the data is not resident in the cache, a cache “miss” occurs, and the system retrieves the data from main memory. Frequently utilized data thus is retrieved more rapidly than less frequently requested data, and overall data access latency, i.e. time between a request for data and delivery of the data, is reduced. In associative mapping, instead of hard-allocating cache lines to particular memory locations, it is possible to design the cache so that any line can store the contents of any memory location. A cache line is the smallest unit of memory than can be transferred between the main memory and the cache. Associativity improves performance by, in part, enabling multiple concurrent accesses to portions of memory. Relatively large amounts of bandwidth are needed to support associativity, however. On some processor memory architectures, for instance, the x86, there is not enough memory bandwidth (the amount of data that can be carried from one point to another in a given time period) to support a cache with associativity. The inability to support cache access with associativity relegates manufacturers to using other, less efficient forms of memory access and lower performance. Consequently, what is needed is an improved manner of managing memory in a system comprising a processor with directly attached memory.

4.125

4

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Drosophila reproductive behavior will be studied using genetic tools. Questions on the control, by the various parts of the nervous system, of different features of courtship will be asked with genetic mosaics (following up our earlier studies). What parts of the dorsal brain must be male to allow the early steps of courtship to be performed? Are intermediate steps of courtship controlled by the brain, and if so, by the same parts? The later steps of courtship are controlled by male thoracic tissues: is the thoracic ganglion critically involved in such control? For female behaviors, which tissues must have a female genotype in order that a mosaic be receptive to courtship and copulation, or be able to carry out the post-copulation rejection behaviors? -- Several behavioral mutants affecting courtship have been characterized by behavioral observation and manipulation. Different mutants influence the early, middle, or late stages of courtship sequence. The causes of these reproductive defects will be analyzed, beginning with studies of mosaics: For instance, where in the fly must a small genetic duplication--carrying the normal allele of a gene involved in aberrant male-female and male-male interactions--be present in order that normal behavior occur? Some of the experiments here, on mutants and mosaics, will concern the possible genetic control of particular neural oscillators--those that drive motor output in the courtship lovesong. Also, we are dissecting the control of copulation--its basic duration, the relationship of that duration to sperm transfer, and the details of actions involved in its termination. -- The various mutants may affect the development or the functioning of the nervous system. In this light, we will analyze conditional alleles of certain of the mutants, to ask which stage of the life cycle is influenced by the genetic variants. -- We are asking several questions on triggers and inhibitions of courtship behaviors, influenced by putative pheromones. These experiments are related, not only to studies of normal males and females, but also very strongly to the investigations of behavioral mutants, and to the behavioral dissection of the brain in genetic mosaics.

3.25

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Q: Scanf with a specific format I would like to allow the user to only put input in a specific format.The format: a=1,b=-2,c=3 for example. Spaces are allowed inbetween the commas and the characters.I'm using: if (scanf("a=%lf,b=%lf,c=%lf",&a,&b,&c) == 1) but for some reason it doesn't work. How can I fix it? A: You are converting 3 numbers, the return value should be 3 if all conversions are successful. Also note that %lf ignores spaces before the number. If you also want to ignore spaces around the , and before the = or the a, add a space in the format string: double a, b, c; if (scanf(" a =%lf , b =%lf , c =%lf", &a, &b, &c) == 3) { /* conversion was successful, 3 numbers parsed */ ... } Note however that scanf() will not ignore just space characters, it will ignore and whitespace characters, including newlines, tabs, etc.

3.09375

3

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- 18384239 = 0. Let v = b - -11270494. What is v rounded to the nearest 1000000? 5000000 Let x = -80910709 - -80907455.86056. Let g = x + 3253. Let y = -0.14 - g. Round y to four decimal places. -0.0006 Let u = -0.105 - 0.009. What is u rounded to two decimal places? -0.11 Let y = -0.109956 - -0.11. What is y rounded to 5 dps? 0.00004 Let y = 2132261743607.5999992 + -2132262623126. Let i = 879518 + y. Let d = i + 0.4. Round d to six decimal places. -0.000001 Let j = 222831 + -119831. What is j rounded to the nearest 10000? 100000 Let g = 0.38 - 0.38000006. Round g to seven dps. -0.0000001 Let z = 0 - 0. Let w = 0.3 + z. Let t = -0.82 + w. What is t rounded to 1 decimal place? -0.5 Let d = -0.037 + 0.0369884. Round d to six dps. -0.000012 Let t be 20/(990003/(-330000) - -3). Round t to the nearest 1000000. -2000000 Let s = -8.94 - -9. Let u = 0.0599968 - s. What is u rounded to 6 dps? -0.000003 Let i = 2.6 - 3.16. Let h = i + 0.56000049. What is h rounded to seven decimal places? 0.0000005 Let l be (-4)/(-6) + (-13)/(-3). Let o(s) = -l + 3 + 229*s + 0. Let b be o(-2). Round b to the nearest 100. -500 Let f = -7.89999794 + 7.9. Round f to six dps. 0.000002 Let x(f) = -f**3 + 2*f**2 + 2*f - 2. Let t be x(2). Suppose -t*v + 3*v = -14800. Round v to the nearest 1000. -15000 Let i = 4 - 3.95. Let b = i - 0.04999999. What is b rounded to 7 dps? 0 Let m = 67 + -21. Let x = m + -45.99939. Round x to 4 dps. 0.0006 Suppose 2*l + 0*q - 5*q = 2132846, -4*l + 4265702 = -5*q. Suppose -16666428 + l = -3*k. Round k to the nearest one million. 5000000 Let p = -30 + 19. Let t = 11.0065 + p. What is t rounded to three dps? 0.007 Let d = -387.36 + 267.67. Let n = d + 119. Round n to one dp. -0.7 Let p = -5462.1 - -5462.293272. Let o = p + -0.1634. Let j = o - 0.03. What is j rounded to five dps? -0.00013 Let u = -55.034 + 55. Let d = -6607.97300059 + 6607.939. Let l = d - u. What is l rounded to seven decimal places? -0.0000006 Let v = 16 - 27. Let o = v - -10.99999998. Round o to 7 decimal places. 0 Let o = 5.8 + 1.5. What is o rounded to 0 decimal places? 7 Suppose -2*f + 2160000 = f. What is f rounded to the nearest 100000? 700000 Let p be 5 + -3 + 0/2. Suppose -v + 5*o + 362893 = -227107, 1770000 = 3*v - p*o. Round v to the nearest 100000. 600000 Let f = -0.39 + 4.19. Let r = f - 3.46. Let b = r - 0.5. Round b to 1 dp. -0.2 Let l = 6.91 + -0.01. Let v = l + 0.1. Let b = v + -14.9. Round b to the nearest integer. -8 Let i = -2.81 - -2.7. Let f = i + 4.61. Let g = 5 - f. Round g to the nearest integer. 1 Let n = 7 - 6. Let b = n - 1.000064. Round b to 5 dps. -0.00006 Suppose 1440 = -5*k + f - 2107, -k - 3*f - 719 = 0. What is k rounded to the nearest 100? -700 Let f = 3.58 + -3.58507. What is f rounded to 3 decimal places? -0.005 Let b be 35*-1*(-8)/(-4). What is b rounded to the nearest one hundred? -100 Suppose 202439 = c - 51561. What is c rounded to the nearest 10000? 250000 Let g = 2026 + -2024.817. Let i = -0.033 + g. Round i to 1 dp. 1.2 Let w be 0 - -3 - (-12)/(-3). Let r(m) = -518453*m - 471987*m + 150441*m + 1. Let g be r(w). What is g rounded to the nearest 100000? 800000 Let f(m) = 2 - 3*m**2 + 2 - 2*m**3 + m**2 + 5*m. Let v be (-10)/3 + (-3)/(-9). Let r be f(v). What is r rounded to the nearest ten? 30 Let r = 62.00082 - 62. What is r rounded to four dps? 0.0008 Let c = 84007713652373762.99999858 + -84007714656568843. Let y = 1004195038 + c. Let k = -42 - y. Round k to seven decimal places. 0.0000014 Let m = 551411 + 4079038. Suppose 5*t + 0*h = -3*h + 24347743, -24347771 = -5*t + 4*h. Let f = m + t. Round f to the nearest one million. 10000000 Let s = -6 + -6. Let q be s/(-7) + 10/35. Suppose -q*l = -3*w + 620000, -w = l - 0*w + 310000. Round l to the nearest 100000. -300000 Let x = 1.8 + 0.2. Let n = -146.025 - -148. Let p = x - n. What is p rounded to 2 dps? 0.03 Let r = -8 - -8.006. Let z = r + 39.994. Let q = 40.0043 - z. Round q to 3 dps. 0.004 Suppose 0 = f - 6 + 2. Suppose -2*u - f*g - 155008 = 3*u, -u - 3*g - 31006 = 0. What is u rounded to the nearest ten thousand? -30000 Let m = -0.49 - -0.48883. Round m to four dps. -0.0012 Let s = -23.894 + 24. Let q = s + -0.10599951. What is q rounded to 7 decimal places? 0.0000005 Let g = -1656177 - -966177. Round g to the nearest 100000. -700000 Let n be (-3)/((6/2)/(-3)). Suppose 0 = 7*m - n*m + 22400000. What is m rounded to the nearest one million? -6000000 Let s = 540037.15900084 + -540015.159. Let f = s + -22. Round f to seven decimal places. 0.0000008 Let d = 148 + -147.701. Let h = -0.044 + d. Let f = h - 0.025. Round f to one dp. 0.2 Let n = -9 - -3. Let b = -0.3546 - -6.35364. Let s = n + b. Round s to 4 decimal places. -0.001 Let t = -82 - -81.9392. Let p = 0.06 + t. What is p rounded to 3 decimal places? -0.001 Let j = 3.32 + -3.3199358. What is j rounded to five decimal places? 0.00006 Suppose -n - 418 = -0*n. Let l = 1918 + n. What is l rounded to the nearest one hundred? 1500 Let x(f) = -2*f - 1. Let v be x(-4). Let i(y) = -13264*y**2 - 10*y + 6. Let g be i(v). Round g to the nearest 100000. -700000 Let n = -0.325 - -0.3. Let d = 0 + n. What is d rounded to 2 dps? -0.03 Let d = -7 - -5.9. Let y = d + 1.1065. Round y to three decimal places. 0.007 Let l = 83 + -79.7. What is l rounded to the nearest integer? 3 Let n = -0.14 + 0.38. Let t = 1.86 + n. Round t to 0 decimal places. 2 Let y be 3 - (-24000 + 1 + 2). Suppose -5*w = -w + y. What is w rounded to the nearest ten thousand? -10000 Let f = 1.02 - -60.98. Let a = 4938.54 - 4876. Let s = f - a. What is s rounded to one decimal place? -0.5 Let b = 8181890539 - 8181891304.0734971. Let p = -764.3935 - b. Let j = p - 0.68. Round j to six decimal places. -0.000003 Let u = -16.35 - -0.55. Let w = u + 15.799889. What is w rounded to five decimal places? -0.00011 Let b = -11.23 + -0.45. Let k = b + -0.02. What is k rounded to 0 dps? -12 Let n(k) be the first derivative of -k**5/3 - k**4/24 - 2*k**3/3 - 1. Let i(x) be the third derivative of n(x). Let m be i(1). Round m to the nearest ten. -40 Let u = -11.09 + 11. Let h = u - -0.0899912. Round h to six dps. -0.000009 Let a(n) = n**2 - 3*n - 1. Let g be a(2). Let s be g/(-9) - 2701/3. Round s to the nearest 1000. -1000 Let d = 0.04449 + 0.41145. Let r = d - -0.14436. Let s = -0.6 + r. What is s rounded to 4 decimal places? 0.0003 Let x = 14 - 13.9949. What is x rounded to 3 decimal places? 0.005 Let a = -0.045381 + -2874.804619. Let j = a - -2874.969981. Let h = 0.12 - j. What is h rounded to five decimal places? 0.00002 Suppose -2*c = 3*c - 3*g - 21, 4*g - 4 = -4*c. Suppose -350 = -a - 2*a + 2*v, -a = -c*v - 105. What is a rounded to the nearest ten? 120 Let v = -2127942 + -10072058. What is v rounded to the nearest 1000000? -12000000 Let t = 30.6 + -16.3. Let x = -14.2999882 + t. What is x rounded to six decimal places? 0.000012 Let x = -0.1 + 1.2. What is x rounded to 0 dps? 1 Let r = 11 - 13. Let p = r + 1.999967. What is p rounded to 5 dps? -0.00003 Let a(i) = -i + 1 - 3 - 2 + i**3 - 4*i**2 + 6*i. Let m be a(3). What is m rounded to the nearest integer? 2 Suppose 116 = -4*p + 3*q - 234, 4*p + 2*q + 340 = 0. Let h be p + 2/(-5 - -3). Round h to the nearest 10. -90 Let g(k) = 4 + 5*k**2 + 0 - 4*k**2 + 5*k. Let j be g(-4). Let f(z) = z**3 - 1190000. Let h be f(j). Round h to the nearest one hundred thousand. -1200000 Let a = -54.2952 + -0.0048. Let o = a - -49. What is o rounded to the nearest integer? -5 Let p = 7336511 - 7336512.7999993. Let d = 1.8 + p. Round d to seven decimal places. 0.0000007 Let f = 13449710 - 8949710. What is f rounded to the nearest 1000000? 5000000 Suppose 3*f + 62935 = -2*f. Let n = -24587 - f. Round n to the nearest 10000. -10000 Let m be (-89200003)/(-4) - 15/20. What is m rounded to the nearest one million? 22000000 Suppose 2*k + 21664 = k - 2*h, -4*k = -2*h + 86616. Let s = -5969 - k. Let f = s - 108687. Round f to the nearest ten thousand. -90000 Suppose -4*v - 2 = -2*l, -4*l + 0*l + 12 = -4*v. Suppose 0 = -v*i + 5*i - 14700. Round i to the nearest 1000. 5000 Suppose 12*p = 8*p - 16. Let c be p/(-8)*8 + -1304. What is c rounded to the nearest one thousand? -1000 Let j = -9 + 10. Let h be 1*((1 - -1) + j). Suppose -2300000 = 2*o - h*o. Round o to the near

3

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