Chapter 6. Evolution of the Brain and Behavior
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by Sarah Zielinski When you get a phone call or a text from a friend or acquaintance, how fast you respond — or whether you even bother to pick up your phone — often depends on the quality of the relationship you have with that person. If it’s your best friend or mom, you probably pick up right away. If it’s that annoying coworker contacting you on Sunday morning, you might ignore it. Ring-tailed lemurs, it seems, are even pickier in who they choose to respond to. They only respond to calls from close buddies, a new study finds. These aren’t phone calls but contact calls. Ring-tailed lemurs live in female-dominated groups of 11 to 16, and up to 25, animals, and when the group is on the move, it’s common for one member to yell out a “meow!” and for other members to “meow!” back. A lemur may also make the call if it gets lost. The calls serve to keep the group together. The main way ring-tailed lemurs (and many other primates) build friendships, though, is through grooming. Grooming helps maintain health and hygiene and, more importantly, bonds between members. It’s a time-consuming endeavor, and animals have to be picky about who they bother to groom. Ipek Kulahci and colleagues at Princeton University wanted to see if there was a link between relationships built through grooming and vocal exchanges among ring-tailed lemurs. Contact calls don’t require nearly as much time or effort as grooming sessions, so it is possible that animals could be less discriminating when they respond to calls. But, the researchers reasoned, if the vocalizations were a way of maintaining the relationships built through painstaking grooming sessions, then the lemurs would be as picky in their responses as in their grooming partners. © Society for Science & the Public 2000 - 2015.
By Elahe Izadi Tiny cameras attached to wild New Caledonian crows capture, for the first time, video footage of these elusive birds fashioning hooked stick tools, according to researchers. These South Pacific birds build tools out of twigs and leaves that they use to root out food, and they're the only non-humans that make hooked tools in the wild, write the authors of a study published Wednesday in the journal Biology Letters. Humans have previously seen the crows making the tools in artificial situations, in which scientists baited feeding sites and provided the raw tools; but researchers say the New Caledonian crows have never been filmed doing this in a completely natural setting. "New Caledonian crows are renowned for their unusually sophisticated tool behavior," the study authors write. "Despite decades of fieldwork, however, very little is known about how they make and use their foraging tools in the wild, which is largely owing to the difficulties in observing these shy forest birds." Study author Jolyon Troscianko of the University of Exeter in England described the tropical birds as "notoriously difficult to observe" because of the terrain of their habitat and their sensitivity to disturbance, he said in a press release. "By documenting their fascinating behavior with this new camera technology, we obtained valuable insights into the importance of tools in their daily search for food," he added.
Carl Zimmer Over the past few million years, the ancestors of modern humans became dramatically different from other primates. Our forebears began walking upright, and they lost much of their body hair; they gained precision-grip fingers and developed gigantic brains. But early humans also may have evolved a less obvious but equally important advantage: a peculiar sleep pattern. “It’s really weird, compared to other primates,” said Dr. David R. Samson, a senior research scientist at Duke University. In the journal Evolutionary Anthropology, Dr. Samson and Dr. Charles L. Nunn, an evolutionary biologist at Duke, reported that human sleep is exceptionally short and deep, a pattern that may have helped give rise to our powerful minds. Until recently, scientists knew very little about how primates sleep. To document orangutan slumber, for example, Dr. Samson once rigged up infrared cameras at the Indianapolis Zoo and stayed up each night to watch the apes nod off. By observing their movements, he tracked when the orangutans fell in and out of REM sleep, in which humans experience dreams. “I became nocturnal for about seven months,” Dr. Samson said. “It takes someone who wants to get their Ph.D. to be motivated enough to do that.” In the new study. Dr. Samson and Dr. Nunn combined that information with studies of 19 other primate species. The researchers found wide variations in how long the animals slept. Mouse lemurs doze for seventeen hours a day, for example, while humans sleep just seven hours or so a day — “the least of any primate on the planet,” said Dr. Samson. © 2015 The New York Times Company
Megan Scudellari In 1997, physicians in southwest Korea began to offer ultrasound screening for early detection of thyroid cancer. News of the programme spread, and soon physicians around the region began to offer the service. Eventually it went nationwide, piggybacking on a government initiative to screen for other cancers. Hundreds of thousands took the test for just US$30–50. LISTEN James Harkin, a researcher for the British TV trivia show QI, talks to Adam Levy about how he finds facts and myths for the show — and then runs a mini-quiz to see whether the Podcast team can discern science fact from science fiction 00:00 Across the country, detection of thyroid cancer soared, from 5 cases per 100,000 people in 1999 to 70 per 100,000 in 2011. Two-thirds of those diagnosed had their thyroid glands removed and were placed on lifelong drug regimens, both of which carry risks. Such a costly and extensive public-health programme might be expected to save lives. But this one did not. Thyroid cancer is now the most common type of cancer diagnosed in South Korea, but the number of people who die from it has remained exactly the same — about 1 per 100,000. Even when some physicians in Korea realized this, and suggested that thyroid screening be stopped in 2014, the Korean Thyroid Association, a professional society of endocrinologists and thyroid surgeons, argued that screening and treatment were basic human rights. © 2015 Nature Publishing Group,
Parrots can dance and talk, and now apparently they can use and share grinding tools. They were filmed using pebbles for grinding, thought to be a uniquely human activity – one that allowed our civilisations to extract more nutrition from cereal-based foods. Megan Lambert from the University of York, UK, and her colleagues were studying greater vasa parrots (Coracopsis vasa) in an aviary when they noticed some of the birds scraping shells in their enclosure with pebbles and date pips. “We were surprised,” says Lambert. “Using tools [to grind] seashells is something never seen before in animals.” Afterwards, the birds would lick the powder from the tool. Some of the parrots even passed tools to each other, which is rarely seen in animals. This behaviour was exclusively male to female. Lambert and her team, who watched the parrots for six months, noticed that the shell-scraping was more frequent before their breeding season. Since seashells contain calcium, which is critical for females before egg-laying, they suspect that the parrots could be manufacturing their own calcium supplements, as the mineral is probably better absorbed in powder form. Greater vasa parrots are native to Madagascar and have breeding and social systems unique among parrots. For example, two or more males have an exclusive sexual relationship with two or more females, and they are unusually tolerant of their group members. The reproductive ritual of sharing tools and grinding could be yet another one of their quirks. © Copyright Reed Business Information Ltd.
By Kelli Whitlock Burton Evolutionarily speaking, we are born to make babies. Our bodies—and brains—don’t fall apart until we come to the end of our child-bearing years. So why are grandmothers, who don’t reproduce and who contribute little to food production, still around and still mentally sound? A new study offers an intriguing genetic explanation. Scientists have proposed several explanations for why our species lives as long and as healthily as it does. One idea is that grandmothers help out with child rearing. A 1998 study found, for example, that a Hadza group of hunter-gatherers in Tanzania had more babies if grandmothers helped feed their newly-weaned young grandchildren. The researchers speculated this kind of care freed up young mothers to reproduce, and ensured that the caregiver grandmother’s genes were passed on to more young. They called their theory the “grandmother hypothesis.” But grandmothers need to have all their wits about them to help out in this way, and the new study may explain how this happens. Physician-scientist Ajit Varki and evolutionary biologist Pascal Gagneux of the University of California, San Diego, arrived at the findings accidentally. The pair was studying a gene that helps control the body’s inflammatory and immune response to injury or infection. Previous studies have linked two forms of the gene—CD33—to Alzheimer’s disease. While one CD33 variant, or allele, predisposes a person to the disease, the other appears to protect against it by preventing the formation of protein clumps in the brain. © 2015 American Association for the Advancement of Science.
By Diana Kwon The human brain is unique: Our remarkable cognitive capacity has allowed us to invent the wheel, build the pyramids and land on the moon. In fact, scientists sometimes refer to the human brain as the “crowning achievement of evolution.” But what, exactly, makes our brains so special? Some leading arguments have been that our brains have more neurons and expend more energy than would be expected for our size, and that our cerebral cortex, which is responsible for higher cognition, is disproportionately large—accounting for over 80 percent of our total brain mass. Suzana Herculano-Houzel, a neuroscientist at the Institute of Biomedical Science in Rio de Janeiro, debunked these well-established beliefs in recent years when she discovered a novel way of counting neurons—dissolving brains into a homogenous mixture, or “brain soup.” Using this technique she found the number of neurons relative to brain size to be consistent with other primates, and that the cerebral cortex, the region responsible for higher cognition, only holds around 20 percent of all our brain’s neurons, a similar proportion found in other mammals. In light of these findings, she argues that the human brain is actually just a linearly scaled-up primate brain that grew in size as we started to consume more calories, thanks to the advent of cooked food. Other researchers have found that traits once believed to belong solely to humans also exist in other members of the animal kingdom. Monkeys have a sense of fairness. Chimps engage in war. Rats show altruism and exhibit empathy. In a study published last week in Nature Communications, neuroscientist Christopher Petkov and his group at Newcastle University found that macaques and humans share brain areas responsible for processing the basic structures of language. © 2015 Scientific American
by Sarah Zielinski Call someone a “bird brain” and they are sure to be offended. After all, it’s just another way of calling someone “stupid.” But it’s probably time to retire the insult because scientists are finding more and more evidence that birds can be pretty smart. Consider these five species: We may call pigeons “flying rats” for their penchant for hanging out in cities and grabbing an easy meal. (Long before there was “pizza rat,” you know there had to be “pizza pigeons” flying around New York City.) But there may be more going on in their brains than just where to find a quick bite. Richard Levenson of the University of California, Davis Medical Center and colleagues trained pigeons to recognize images of human breast cancers. In tests, the birds proved capable of sorting images of benign and malignant tumors. In fact, they were just as good as humans, the researchers report November 18 in PLOS ONE. In keeping with the pigeons’ reputation, though, food was the reward for their performance. No one would suspect the planet’s second-best toolmakers would be small black birds flying through mountain forests on an island chain east of Australia. But New Caledonian crows have proven themselves not only keen toolmakers but also pretty good problem-solvers, passing some tests that even dogs (and pigeons) fail. For example, when scientists present an animal with a bit of meat on a long string dangling down, many animals don’t ever figure out how to get the meat. Pull it up with one yank, and the meat is still out of reach. Some animals will figure out how to get it through trial and error, but a wild New Caledonian crow solved the problem — pull, step on string, pull some more — on its first try. © Society for Science & the Public 2000 - 2015
Human DNA is 1 to 2% Neandertal, or more, depending on where your ancestors lived. Svante Pääbo, founder of the field of paleogenetics and winner of a 2016 Breakthrough Prize, explains why that matters © 2015 Scientific American
Jon Hamilton Patterns of gene expression in human and mouse brains suggest that cells known as glial cells may have helped us evolve brains that can acquire language and solve complex problems. Scientists have been dissecting human brains for centuries. But nobody can explain precisely what allows people to use language, solve problems or tell jokes, says Ed Lein, an investigator at the Allen Institute for Brain Science in Seattle. "Clearly we have a much bigger behavioral repertoire and cognitive abilities that are not seen in other animals," he says. "But it's really not clear what elements of the brain are responsible for these differences." Research by Lein and others provides a hint though. The difference may involve brain cells known as glial cells, once dismissed as mere support cells for neurons, which send and receive electrical signals in the brain. Lein and a team of researchers made that finding after studying which genes are expressed, or switched on, in different areas of the brain. The effort analyzed the expression of 20,000 genes in 132 structures in brains from six typical people. Usually this sort of study is asking whether there are genetic differences among brains, Lein says. "And we sort of flipped this question on its head and we asked instead, 'What's really common across all individuals and what elements of this seem to be unique to the human brain?' " he says. It turned out the six brains had a lot in common. © 2015
Ewen Callaway A long stretch of DNA called a supergene explains the variety of bizarre tactics that a wading bird species deploys to win mates, a pair of genome-sequencing studies concludes1, 2. Common to marshes and wet meadows in northern Europe and Asia, ruffs (Philomachus pugnux) are named after the decorative collars popular in Renaissance Europe. But the birds’ poufy plumage is not the only baroque aspect of their biology. Males gather at mass breeding grounds where they juke, jump and lunge toward other males, in hopes of winning females. Male ruffs belong to one of three different forms, each with a unique approach to mating. 'Independent' males, with hodgepodge of brown and black neck feathers, are territorial and defend their bit of the breeding ground. White-feathered 'satellite' males, by contrast, invade the turf of independents to steal nearby females. A third, rarer form, called 'faeders' (Old English for father), take advantage of their resemblance to female ruffs to interrupt coital encounters. “They dash in and jump on the female before the territorial males does,” says Terry Burke, an evolutionary biologist at University of Sheffield, UK. “My colleague describes this as the 'sandwich'. You end up with the territorial male jumping on the back of the mimic.” Burke was part of a team that, in 1995, found that the different approaches of male ruffs were caused by a single inherited factor3. But it seemed improbable that one gene could trigger such wide-ranging differences in behaviour and appearance. © 2015 Nature Publishing Group
By Virginia Morell Plunge a live crab into a pot of boiling water, and it’s likely to try to scramble out. Is the crab’s behavior simply a reflex, or is it a sign of pain? Many scientists doubt that any invertebrate (or fish) feels pain because they lack the areas in the brain associated with human pain. Others argue this is an unfair comparison, noting that despite the major differences between vertebrate and invertebrate brains, their functions (such as seeing) are much the same. To get around this problem, researchers in 2014 argued that an animal could be classified as experiencing pain if, among other things, it changes its behavior in a way that indicates it’s trying to prevent further injury, such as through increased wariness, and if it shows a physiological change, such as elevated stress hormones. To find out whether crabs meet these criteria, scientists collected 40 European shore crabs (Carcinus maenas), shown in the photo above, in Northern Ireland. They placed the animals into individual tanks, and gave half 200-millisecond electrical shocks every 10 seconds for 2 minutes in their right and left legs. The other 20 crabs served as controls. Sixteen of the shocked crabs began walking in their tanks, and four tried to climb out. None of the control crabs attempted to clamber up the walls, but 14 walked, whereas six didn’t move at all. There was, however, one big physiological difference between the 16 shocked, walking crabs and the 14 control walkers, the scientists report in today’s issue of Biology Letters: Those that received electrical jolts had almost three times the amount of lactic acid in their haemolymph, a fluid that’s analogous to the blood of vertebrates—a clear sign of stress. Thus, crabs pass the bar scientists set for showing that an animal feels pain. © 2015 American Association for the Advancement of Science.
By Jason G. Goldman When a monkey has the sniffles or a headache, it doesn't have the luxury of popping a few painkillers from the medicine cabinet. So how does it deal with the common colds and coughs of the wildlife world? University of Georgia ecologist Ria R. Ghai and her colleagues observed a troop of more than 100 red colobus monkeys in Uganda's Kibale National Park for four years to figure out whether the rain forest provides a Tylenol equivalent. Monkeys infected with a whipworm parasite were found to spend more time resting and less time moving, grooming and having sex. The infected monkeys also ate twice as much tree bark as their healthy counterparts even though they kept the same feeding schedules. The findings were published in September in the journal Proceedings of the Royal Society B. The fibrous snack could help literally sweep the intestinal intruder out of the simians' gastrointestinal tracts, but Ghai suspects a more convincing reason. Seven of the nine species of trees and shrubs preferred by sick monkeys have known pharmacological properties, such as antisepsis and analgesia. Thus, the monkeys could have been self-medicating, although she cannot rule out other possibilities. The sick individuals were, however, using the very same plants that local people use to treat illnesses, including infection by whipworm parasites. And that “just doesn't seem like a coincidence,” Ghai says. © 2015 Scientific American,
Angus Chen English bursts with consonants. We have words that string one after another, like angst, diphthong and catchphrase. But other languages keep more vowels and open sounds. And that variability might be because they evolved in different habitats. Consonant-heavy syllables don't carry very well in places like windy mountain ranges or dense rainforests, researchers say. "If you have a lot of tree cover, for example, [sound] will reflect off the surface of leaves and trunks. That will break up the coherence of the transmitted sound," says Ian Maddieson, a linguist at the University of New Mexico. That can be a real problem for complicated consonant-rich sounds like "spl" in "splice" because of the series of high-frequency noises. In this case, there's a hiss, a sudden stop and then a pop. Where a simple, steady vowel sound like "e" or "a" can cut through thick foliage or the cacophony of wildlife, these consonant-heavy sounds tend to get scrambled. Hot climates might wreck a word's coherence as well, since sunny days create pockets of warm air that can punch into a sound wave. "You disrupt the way it was originally produced, and it becomes much harder to recognize what sound it was," Maddieson says. "In a more open, temperate landscape, prairies in the Midwest of the United States [or in Georgia] for example, you wouldn't have that. So the sound would be transmitted with fewer modifications." © 2015 npr
Natasha Gilbert The eye-catching plumage of some male songbirds has long been explained as a result of sexual selection: brighter males compete more successfully for mates, so evolution favours their spread. Females, by contrast, remain drab. A new study turns this explanation on its head. Sexual-selection pressures drive females to evolve dull feathers more strongly than they drive males to become colourful, argues James Dale, an evolutionary ecologist at Massey University in Auckland, New Zealand. That surprising conclusion is based on a data set of plumage colour in nearly 6,000 songbirds, which Dale and his colleagues built. They used their data to ask how various potential evolutionary factors drive male and female plumage colour. If a particular songbird species was polygynous (that is, the males had more than one mate), displayed a large difference in size between males and females, and left care of the young mainly up to the females, then the researchers judged that sexual selection was likely to be an important factor in that species' evolution. The study, published in Nature1, found that sexual selection does play an important role in creating colour differences between male and female plumage. But the contrast is largely driven by females evolving to become drab. “Females are the chief architect of the difference,” says Dale. © 2015 Nature Publishing Group
By Hanae Armitage Schools of fish clump together for a very simple reason: safety in numbers. But for some, banding together offers more than just protection. It’s a way of getting to the head of the class. Schooling fish learn from each other, and new research shows that when they’re taken out of their normal social group, individuals struggle to learn on their own. Scientists have long known that schooling fish observe and learn from each other’s failures and successes, behaviors that stimulate neural development, especially in the part of the brain responsible for memory and learning. But this is the first time they have found evidence of that link in spatial learning. To test their theory, scientists divided a school of social cichlid fish into two categories: 14 social fish and 15 loners. Researchers kept the social fish grouped together while they partitioned the loners into single-fish isolation tanks. They ran both groups through a simple T-shaped maze, color coding the side that harbored food—a yellow mark for food, a green mark for no food. Seven of the 14 socialized fish learned to associate yellow with food (high marks for the cichlids, which are not the brightest fish in the animal kingdom), whereas only three of the 15 isolated fish successfully made the same association. Writing in this month’s issue of Applied Animal Behaviour Science, the researchers say this suggests fish in group settings are able to learn better and faster than their singled out counterparts. The moral? Simple: Fish should stay in school. © 2015 American Association for the Advancement of Science
Carl Zimmer In recent years, a peculiar sort of public performance has taken place periodically on the sidewalks of Seattle. It begins with a woman named Kaeli N. Swift sprinkling peanuts and cheese puffs on the ground. Crows swoop in to feed on the snacks. While Ms. Swift observes the birds from a distance, notebook in hand, another person walks up to the birds, wearing a latex mask and a sign that reads “UW CROW STUDY.” In the accomplice’s hands is a taxidermied crow, presented like a tray of hors d’oeuvres. This performance is not surreal street theater, but an experiment designed to explore a deep biological question: What do crows understand about death? Ms. Swift has been running this experiment as part of her doctoral research at the University of Washington, under the guidance of John M. Marzluff, a biologist. Dr. Marzluff and other experts on crow behavior have long been intrigued by the way the birds seem to congregate noisily around dead comrades. Dr. Marzluff has witnessed these gatherings many times himself, and has heard similar stories from other people. “Whenever I give a talk about crows, there’s always someone who says, ‘Well, what about this?’ ” he said. Dr. Marzluff and Ms. Swift decided to bring some scientific rigor to these stories. They wanted to determine whether a dead crow really does trigger a distinctive response from living crows and, if so, what the purpose of the large, noisy gatherings might be. To run the experiment, Ms. Swift began by delivering food to a particular spot each day, so that the crows learned to congregate there to eat. Then one of her volunteers would approach the feast with a dead crow, and Ms. Swift observed how the birds reacted. © 2015 The New York Times Company
By Jon Cohen A virus that long ago spliced itself into the human genome may play a role in amyotrophic lateral sclerosis (ALS), the deadly muscle degenerative disease that crippled baseball great Lou Gehrig and ultimately took his life. That’s the controversial conclusion of a new study, which finds elevated levels of human endogenous retrovirus K (HERV-K) in the brains of 11 people who died from the disease. “This certainly is interesting and provocative work,” says Raymond Roos, a neurologist at the University of Chicago in Illinois who treats and studies ALS but who was not involved with the finding. Still, even the scientists behind the work caution that more research is needed to confirm the link. “I’m very careful to say HERV-K doesn’t cause the disease but may play a role in the pathophysiology,” says study leader Avindra Nath, a neuroimmunologist at the National Institute of Neurological Disorders and Stroke in Bethesda, Maryland. “The darn thing is in the chromosomes to begin with. It’s going to be very hard to prove causation.” It was another retrovirus, HIV, that led Nath to first suspect a connection between viruses and ALS. In 2006, he was helping a patient control his HIV infection with antiretroviral drugs when he noticed that the man’s ALS also improved. “That intrigued me, and I looked in the ALS literature and saw that people had reported they could see reverse transcriptase in the blood.” Reverse transcriptase, an enzyme that converts RNA to DNA, is a hallmark of retroviruses, which use it to insert copies of their genes into chromosomes of their hosts. © 2015 American Association for the Advancement of Science
Are you good at picking someone out of a crowd? Most of us are better at recognising faces than distinguishing between other similar objects, so it’s long been suspected there’s something mysterious about the way the brain processes a face. Now further evidence has emerged that this is a special, highly evolved skill. A study of twins suggests there are genes influencing face recognition abilities that are distinct from the ones affecting intelligence – so it’s not that people who are good with faces just have a better memory, for instance. “The idea is that telling friend from foe was so important to survival that there was very strong pressure to improve that trait,” says Nicholas Shakeshaft of King’s College London. Previous studies using brain scanning have suggested there is a part of the brain dedicated to recognising faces, called the fusiform face area. But others have suggested this region may in fact just be used for discriminating between any familiar objects. Wondering if genetics could shed any light, Shakeshaft’s team tested more than 900 sets of UK twins – including both identical and non-identical pairs – on their face recognition skills. The ability turned out to be highly heritable, with identical twins having more similar abilities than fraternal ones. The same went for intelligence, which had earlier been tested as part of a long-running study. © Copyright Reed Business Information Ltd.
By Michael Balter Are some animals smarter than others? It’s hard to say, because you can’t sit a chimpanzee or a mouse down at a table for an IQ test. But a new study, in which scientists tested wild robins on a variety of skills, concludes that they do differ in the kind of “general intelligence” that IQ tests are supposed to measure. General intelligence is usually defined as the ability to do well on multiple cognitive tasks, from math skills to problem solving. For years, researchers have questioned whether measurable differences exist in humans and nonhumans alike. In humans, factors like education and socioeconomic status can affect performance. When it comes to animals, the problem is compounded for two main reasons: First, it is very difficult to design and administer tests that pick up on overall smarts instead of specific skills, such as the keen memories of food-hoarding birds or the fine motor skills of chimpanzees that make tools for finding insects in trees. Second, differences in animal test scores can depend on how motivated they are to perform. Because most experiments award would-be test-takers with food, an empty (or a full) stomach might be all it takes to skew the results. Thus, even studies that suggest variations in intelligence among mice, birds, and apes all carry the caveat that alternative explanations could be at play. To get around some of these limitations, a team led by Rachael Shaw, an animal behavior researcher at Victoria University of Wellington, turned to a population of New Zealand North Island robins for a new round of experiments. The robins live at the Zealandia wildlife sanctuary, a 225-hectare nature paradise in Wellington where more than 700 of the birds live wild and protected from predators in the middle of the city. © 2015 American Association for the Advancement of Science.