Shaken-but-not-stirred remnants of Earth’s earliest years still exist nearly 4.6 billion years later.
Researchers traced the shadowy footprints of an isotope that hasn’t existed for over 4.5 billion years to much younger lava rocks from the Pacific and Atlantic oceans. That suggests that reservoirs of the ancient mantle may be hidden deep inside the planet, geochemist Hanika Rizo and colleagues report May 13 in Science.
Earth formed about 4.6 billion to 4.5 billion years ago as planetary bodies collided, disintegrating and melting to accrete into one mass like a hot, rocky lint ball. Geologists have assumed that any relics of this bumpy beginning were mixed beyond recognition. Instead, Rizo’s team found a surprise: Some modern flood basalts have unusually high concentrations of tungsten-182. That’s significant because that isotope forms only from radioactive decay of hafnium-182. And hafnium-182 only existed during Earth’s first 50 million years. “These isotopes had to be created early,” says Rizo, of the University of Quebec in Montreal. It is “spectacular” that some of Earth’s earliest materials may still be preserved, says Matthias Willbold, a geochemist at the University of Manchester in England. “We may have to revise our view of the Earth’s internal structure.”
Rizo and colleagues measured the tungsten-182 in flood basalts from two locations: Canada’s Baffin Bay, part of the 60-million-year-old North Atlantic Igneous Province, and near the Solomon Islands, part of the 120-million-year-old Ontong Java Plateau in the Pacific Ocean. “Flood basalts are not normal eruptions,” Rizo says. “They are capable of tapping into the deep mantle.” Her team found that levels of tungsten-182 in the lavas varied, suggesting that the deep sources of these younger rocks were different pieces of Earth’s oldest material, each with their own isotopic signature and history. These results also show that the ancient remnants have somehow escaped being mixed by convection currents.
Geophysicists have identified two large “blobs” in the deep mantle, called large low-shear velocity provinces. Those blobs “could be candidates” for the remnants of the ancient mantle, Rizo says.
What builds up can also tear down, a new study of bacteria suggests.
Bacteria build biofilms, communities of the microorganisms encased in a protective goo that shields the microbes from antibiotics and immune system attacks. But the very enzymes bacteria use to construct that shield can also destroy some of its molecules and strip away the protection, researchers report May 20 in Science Advances.
“We’re weaponizing the bacteria against themselves,” says P. Lynne Howell, a structural microbiologist at the Hospital for Sick Children in Toronto. Howell and colleagues studied Pseudomonas aeruginosa bacteria, which can cause pneumonia and other infections and is particularly problematic for people with the lung disease cystic fibrosis. The researchers discovered that two enzymes, PelAh and PslGh, which the bacteria use to build two different sugar polymers, can degrade those same polymers. That delete function, supplied by parts of the enzymes known as glycoside hydrolase domains, normally helps correct mistakes or prevents buildup of the sugar chains inside bacterial cells, Howell says.
In laboratory tests, synthetic versions of the glycoside hydrolase domains applied to P. aeruginosa cultures stopped the bacteria from forming new biofilms and melted existing ones. Stripping away sugar polymers did not kill the bacteria but did make them more vulnerable to antibiotics and immune cells. Human lung cells grown in dishes containing the enzymes suffered no harm, suggesting the enzymes wouldn’t damage human tissues.
Animal tests are needed to determine whether the enzymes are safe and can fight biofilm infections in the body, Howell says. Similar enzymes from other bacteria and fungi may also fight biofilm infections caused by those organisms, she says.
Giant pandas have better ears than people — and polar bears. Pandas can hear surprisingly high frequencies, conservation biologist Megan Owen of the San Diego Zoo and colleagues report in the April Global Ecology and Conservation.
The scientists played a range of tones for five zoo pandas trained to nose a target in response to sound. Training, which took three to six months for each animal, demanded serious focus and patience, says Owen, who called the effort “a lot to ask of a bear.”
Both males and females heard into the range of a “silent” ultrasonic dog whistle. Polar bears, the only other bears scientists have tested, are less sensitive to sounds at or above 14 kilohertz. Researchers still don’t know why pandas have ultrasonic hearing. The bears are a vocal bunch, but their chirps and other calls have never been recorded at ultrasonic levels, Owen says. Great hearing may be a holdover from the bears’ ancient past.
Even if you’ve never lived in rattlesnake territory, you know what the sound of a snake’s rattle means: Beware! A shake of its rattle is an effective way for a snake to communicate to a potential predator that an attack could result in a venomous bite.
For more than a century, scientists have posited how that rattle might have evolved. The rattle is composed of segments of keratin (the same stuff that makes up human hair), and specialized muscles in a snake’s tail vibrate those segments rapidly to create the rattling sound. The rattlesnake’s rattle is a trait that evolved only once in the past and is now found in only two closely related genera of snakes that live in North and South America. But plenty of other species of snakes also vibrate their tails as a warning to potential predators.
Bradley Allf and colleagues at the University of North Carolina in Chapel Hill think that the tail vibration and the evolution of the rattle might be connected. They gathered 155 snakes of 56 species — 38 species from the Viperidae family, which includes rattlesnakes, and 18 species from the largest snake family, Colubridae — from museums, zoos and private collectors. Working with captive snakes let them control conditions, such as temperature, that can affect tail vibration. With each snake, one of the researchers tried to get it to behave defensively by waving a stuffed animal in front of it. The team videotaped the snakes as they vibrated their tails, or not.
The researchers plotted the snakes’ tail vibration duration and rate against how closely related a species was to rattlesnakes. One group of snakes that lives in the Americas was taken out of the analysis because its tail vibrations were so similar to those of rattlesnakes; it appears that these species are mimicking the dangerous snakes that live near them (not a bad strategy for survival). Among the rest of the snakes analyzed, those that were more closely related had tail behavior that was more similar to that of rattlesnakes.
“Our results suggest that tail vibration by rattleless ancestors of rattlesnakes may have served as the signal precursor to rattlesnake rattling behavior,” the researchers write in the October issue of the American Naturalist. “If ancestral tail vibration was a reliable cue to predators that a bite was imminent, then this behavior could have become elaborated as a defensive signal.”
Allf and his colleagues propose a couple of ways that this could have happened. Perhaps snakes that made noise with their tails were better at startling predators, and this may have prompted such noise-making tail features to spread and eventually become refined into what is now a rattle. Or maybe snakes that shook their tails longer and faster developed calluses of keratin. If these calluses provided better warning, that may have somehow evolved into a rattle.
“Thus, the rattlesnake rattle might have evolved via elaboration of a simple behavior,” they conclude.
The first time Jessica Cantlon met Kumang at the Seneca Park Zoo, the matriarch orangutan regurgitated her previous meal right into Cantlon’s face. “I was retching,” Cantlon recalls. “It was so gross.” But Cantlon was there to kick off a series of behavioral experiments, and her students, who would be working with Kumang regularly, were watching. “Does anyone have any towels?” she remembers asking, knowing she had to keep her cool.
Cantlon’s deliberate nature and whatever-it-takes attitude have served her well. As a cognitive neuroscientist at the University of Rochester in New York, she investigates numerical thinking with some of the most unpredictable and often difficult study subjects: nonhuman primates, including orangutans, baboons and rhesus macaques, and — most remarkably — children as young as age 3. Both groups participate in cognitive tests that require them, for example, to track relative quantities as researchers sequentially add items to cups and to distinguish between quantities of assorted dots on touch screens. The kids also go into the functional MRI scanner where, in a feat impressive to parents everywhere, they lie completely still for 20 to 30 minutes so Cantlon and colleagues can get pictures of their brains. “She takes steps carefully, and she thinks very hard about where she is going,” says Daniel Ansari, a developmental cognitive neuroscientist at the University of Western Ontario in London, Canada, who is familiar with Cantlon’s work. “She goes for the big questions and big methodological challenges.”
The central question in Cantlon’s research is: How do humans understand numbers and where does that understanding come from? Sub-questions include: What are the most primitive mathematical concepts? What concepts do humans and other primates share? Are these shared concepts the foundation for fancier forms of mathematical reasoning? In addressing these questions, Cantlon draws on a wide range of methods. “Very few people can combine work on cognitive skills — studies from the point of view of behavior — with imaging work in very young children, and very few people do that same combination in nonhuman primates,” says Elissa Newport, who chaired the brain and cognitive sciences department at Rochester for more than a decade and now leads the Center for Brain Plasticity and Recovery at Georgetown University.
As a graduate student, Cantlon determined that neuroimaging studies would add an independent source of data to the cognitive questions under exploration in Elizabeth Brannon’s lab at Duke University. So she identified collaborators and taught herself functional MRI. “By the time she graduated, she had something like four dissertations’ worth of work,” says Brannon, now of the University of Pennsylvania.
In the years since, Cantlon has identified a type of “protocounting” in baboons; they can keep tabs on approximate quantities of peanuts as researchers increase those quantities (SN Online: 5/17/15). In her most attention-grabbing work, Cantlon studied activity in the brains of children while they watched Sesame Street clips that dealt with number concepts — an unexpected success that proved everyday, relatively unaltered stimuli can yield meaningful data. An ongoing study in Cantlon’s lab seeks to find out how monkeys, U.S. kids and adults, and the Tsimané people of Bolivia, who have little formal education, distinguish between quantities. Do they determine the number of dots presented on the computer screen or do they rely on a proxy such as the total area covered by the dots? The work explores how the brain understands everyday concepts, but it could also inform strategies in math education. “If we understand the fundamental nature of the human brain and mind, that might give us a better insight into how to communicate number concepts to kids,” Cantlon says.
Growing up outside of Chicago, Cantlon enjoyed digging deep into a topic and becoming an expert. She and a friend turned themselves into ice skating superfans one summer, reading up on the Olympic skaters and checking videos out of the local library. In another project, Cantlon decided to learn everything possible about the price of gold. When she moved to a school where she could no longer take Latin, she taught and tested herself. Despite the fact that neither of her parents went to college, no one ever questioned that Cantlon would go. She studied anthropology as an undergraduate at Indiana University in Bloomington. “I was interested in the question of where we come from,” Cantlon says. “I was interested in studying people.” During college, she went on an archaeological dig in Belize and studied lemurs in Madagascar. For a year after graduation, she observed mountain gorillas in Rwanda, detailing their behavior every 10 minutes. “What they were thinking was something that was constantly on my mind,” she says. “‘How are we similar? Are you thinking what I’m thinking?’” Though she might have succeeded in any number of careers, she wanted exploration to be a big part of her life: “I don’t think doing a less exotic type of work would have been as satisfying.”
Today, Cantlon, who at age 40 recently earned tenure, doesn’t spend much time in the field. And even in the lab, she leaves much of the data collection to her graduate students and research assistants. “At this point, we are a well-oiled system,” she says, referring to the brain scan studies on kids. To make the kids comfortable, Cantlon’s team does trial runs in a mock scanner, describing it as a spaceship and providing “walkie-talkies” for any necessary communication. To keep them interested, the researchers treat it as a team activity and offer a ton of positive reinforcement, with prizes including Lego sets and a volcano-making kit. The kids receive pictures of their brains, which typically interest the parents most. The older of Cantlon’s two daughters, a 5-year-old extrovert named Cloe, has participated in behavioral tests and will no doubt be excited for her first brain scan.
The Sesame Street study was in part inspired by a paper by Uri Hasson, a neuroscientist at Princeton University who imaged the brains of volunteers while they watched The Good, the Bad and the Ugly. To better understand brain development, Cantlon wanted to see how brain activity compared in kids and adults exposed to math in a natural way. Of particular interest was a region called the intraparietal sulcus, or IPS, thought to play a role in symbolic number processing. The results, reported in PLOS Biology in 2013, showed that kids with IPS activity more closely resembling adults’ activity performed better on mathematical aptitude tests.
“It was the clearest, cleanest — did not have to come out this way — result,” Cantlon says.
Cantlon is notable for her diverse set of tools, says Steve Piantadosi, a computational neuroscientist and colleague at Rochester. “But she has something which is even more powerful than that. If you have different hypotheses and you want to come up with the perfect experiment that distinguishes them, that is something she is very good at thinking about. She is a great combination of critical and creative.”
To add another methodological approach, Cantlon next plans to collaborate with Piantadosi to develop computational models that explain the operations the brain performs as it counts or compares quantities. She would also like to add data analyses from wild primates into the mix. When researchers talk about the evolution of a primitive number sense, they often speak about foraging activity — identifying areas of the forest with more food, for example. But Cantlon wonders whether social interactions also require some basic understanding of quantities.
As for a recent question from a colleague about what risky project she’ll pursue now that she has tenure, Cantlon says nothing in particular comes to mind: “I feel like we’ve been doing the crazy things all along.”
ORLANDO, Fla. — New evidence from separate labs supports the controversial idea that an overlooked and unexpected Culex mosquito might spread Zika virus.
The southern house mosquito, Culex quinquefasciatus, is common in the Americas. Constância Ayres, working with Brazil’s Oswaldo Cruz Foundation in Recife, previously surprised Zika researchers with the disturbing proposal that this mosquito might be a stealth spreader of Zika. But two U.S. research groups tested the basic idea and couldn’t get the virus to infect the species. Now, preliminary results from Ayres’ and two other research groups are renewing the discussion. The data, shared September 26 at the International Congress of Entomology, suggest that Zika can build up in the house mosquito’s salivary glands — a key step in being able to transmit disease. Basic insect physiology is only part of the puzzle, though. Even if the mosquitoes prove competent at passing along Zika, there remain questions of whether their tastes, behavior and ecology will lead them to actually do so.
In the current outbreak, the World Health Organization has focused on mosquitoes in a different genus, Aedes, particularly Ae. aegypti, as the main disease vector. But Ayres had announced months ago the discovery of the virus in Brazil’s free-flying house mosquitoes (SN Online: 7/28/16).
At the congress, Ayres’ foundation colleague Duschinka Guedes reported that captive mosquitoes fed Zika-tainted blood had virus growing in their own guts and salivary glands within days. The virus doesn’t spread every time a mosquito slurping contaminated blood gets virus smeared on its mouthparts, though. To move from the mosquito to what it bites, viruses have to infect the insect midgut, then travel to the salivary glands and build up enough of a population for an infective dose drooling into the next victim. When Guedes offered the infected mosquitoes a special card to bite, they left telltale virus in the salivary traces, a sign of what they could do when biting — and infecting — a real animal.
Researchers from China and Canada who were not originally on the symposium program also stepped up to share their results, some of which are unpublished. Some tasks are still in early stages, but both labs showed Zika virus building up in some kind of Culex mosquitoes.
At the Beijing Institute of Microbiology and Epidemiology, Tong-Yan Zhao found the virus peaking in the house mosquitoes eight days after their first contaminated drink. As a test of the infectious powers of the mosquitoes, researchers let the Zika-carrying insects bite baby lab mice. Later, the virus showed up in the brains of eight out of nine lab mice. The results were reported September 7 in Emerging Microbes & Infections. From Brock University in St. Catharines, Canada, Fiona Hunter has found signs that 11 out of 50 wild-caught Culex pipiens pipiens mosquitoes picked up the virus somewhere on their bodies. So far, she has completely analyzed one mosquito and reports that the virus was indeed in its saliva.
These positive results contradict Culex tests at the University of Texas Medical Branch in Galveston. Those tests, with U.S. mosquitoes, found no evidence that C. quinquefasciatus can pick up and pass along a Zika infection, says study coauthor Scott Weaver. Stephen Higgs of Kansas State University in Manhattan and his colleagues got similar results. “We’re pretty good at infecting mosquitoes,” Higgs says, so he muses over whether certain virus strains won’t infect mosquitoes from particular places.
The main risk from Culex at the moment is distraction, warned Roger Nasci of North Shore Mosquito Abatement District in Northfield, Ill. After the talks, he rose from the audience to say that Ae. aegypti is a known enemy and limited resources should not be diverted from fighting it.
George Peck, who runs mosquito control for Clackamas County in Oregon, isn’t convinced that the high virus concentrations dosing the test mosquitoes are realistic. Yet he’s watching the issue because like much of northern North America, Clackamas doesn’t have the Ae. aegypti vector to worry about. But it does have plenty of Culex mosquitoes.
Using nasal cartilage cells to repair joints is nothing to sniff at.
It has worked in goats. Now, in the first human trial, researchers at the University of Basel in Switzerland have grown cells called chondrocytes, taken from the noses of 10 patients with damaged knee joints, into cartilage grafts. These repair patches were then surgically implanted into the patients’ knee joints.
Two years after surgery, nine patients have seen improvements in knee function, quality of life and pain. (One patient dropped out of the trial because of additional athletic injuries.) MRI scans showed that the grafts looked like normal hyaline cartilage, the hard-to-replicate material that coats the tips of bones, the team reports in the Oct. 22 Lancet. Tests in more people are needed to determine whether the technique is ready for prime time.
Mothers who don’t eat enough during pregnancy could give birth to babies with long-lasting heart problems. The results from a new study in primates add to accumulating evidence that a mother’s nutrition has more bearing on her child’s health than previously thought.
“We pass more biological milestones during development than we will ever pass again in our entire lives,” says Peter Nathanielsz, coauthor of the study published November 6 in the Journal of Physiology. And during those critical nine months, calorie intake at the extremes — too many or too few — appears to have a lifelong influence on newborn weight, future metabolism and chronic health problems (SN: 1/23/16, p. 22). One landmark epidemiological investigation found that people born in the Dutch Hunger Winter during World War II suffered from an elevated risk of heart disease and other health concerns, with some risks even affecting two generations. But studies of human populations are complicated. It’s hard to account for the role of stress, behavior or environmental exposures. So Nathanielsz, of the University of Wyoming in Laramie, and colleagues from the University of Texas Health Science Center at San Antonio studied baboons, close genetic relatives to humans.
Sixteen pregnant baboons were fed their normal amount of chow, while 16 others received 30 percent less during pregnancy, a reduction researchers characterize as “moderate.” All other living conditions were the same. The researchers then compared offspring of the well-fed mothers with the offspring of undernourished mothers.
Infants of the underfed mothers were born small but nonetheless caught up in body weight to the offspring of the well-fed mothers by young adulthood. However, those whose mothers were underfed had more fibrous, abnormally shaped heart muscle, the researchers report. A normal heart is roughly an upside-down pyramid, but underfed offspring had more rounded and less muscular hearts. Evidence showed that these less-muscled hearts were not as efficient at pumping blood, with an average output about 20 percent lower.
Offspring undernourished in the womb also had hearts that appeared to age faster. By age five, the human equivalent of almost 25, many of their heart functions more closely resembled those of hearts of primates about three times as old.
Such experiments can show cause and effect — something that human studies can’t do, says Susan Ozanne, a developmental endocrinologist at the University of Cambridge. As a result, they provide strong evidence about the effects of maternal nutrition. “What this shows us is that certainly maternal diet has an effect on a child’s cardiac health long-term,” she says. Studies in rodents have produced similar findings, but “when you validate those in multiple species, it shows you you’re looking at a fundamentally conserved mechanism.” The next step, she says, is to learn whether diet and exercise after birth can make up for poor nutrition during development. Doctors also don’t know whether there is a window of time during childhood for intervention, or a longer period to counteract any effects, she says.
Much attention on maternal nutrition has focused on the obesity epidemic, Nathanielsz says, but undernutrition remains a public health challenge throughout the world, even in developed countries. The U.S. Department of Agriculture estimates that approximately 13 percent of American households in 2015 reported food insecurity, or uncertainty about having enough money for food. “The number of people with food insecurity is very high,” Nathanielsz says. “It would be sad if we discounted this problem.”
In a rare bright spot for global environmental news, atmospheric scientists reported in 2016 that the ozone hole that forms annually over Antarctica is beginning to heal. Their data nail the case that the Montreal Protocol, the international treaty drawn up in 1987 to limit the use of ozone-destroying chemicals, is working.
The Antarctic ozone hole forms every Southern Hemisphere spring, when chemical reactions involving chlorine and bromine break apart the oxygen atoms that make up ozone molecules. Less protective ozone means that more ultraviolet radiation reaches Earth, where it can damage DNA and lead to higher rates of skin cancer, among other threats. The Montreal Protocol cut back drastically on the manufacture of ozone-destroying compounds such as chlorofluorocarbons, or CFCs, which had been used in air conditioners, refrigerators and other products. It went into force in 1989 and phased out CFCs by 2010.
Earlier studies had hinted that the ozone hole was on the mend. The new work, reported in Science in June, is the most definitive yet (SN: 7/23/16, p. 6). A team led by Susan Solomon, an atmospheric chemist at MIT, looked not only at the month of October, when Antarctic ozone loss typically peaks, but also at September, when the hole is growing. The healing trend was most obvious in September. Satellite measurements showed that from 2000 to 2015, the average extent of the September ozone hole shrank by about 4.5 million square kilometers, to approximately 18 million square kilometers. Soundings taken by weather balloons over Antarctica confirmed the findings. CFC concentrations peaked above Antarctica in the late 1990s and early 2000s and have been dropping ever since, says Birgit Hassler, an atmospheric chemist at Bodeker Scientific in Alexandra, New Zealand. Each passing year allows scientists to gather more convincing data. The new study, Hassler says, “makes the whole development of the Antarctic ozone hole healing very transparent and understandable.” It is a fitting capstone to Solomon’s career. In the 1980s she led a team that proposed that chlorine compounds were to blame for Antarctic ozone loss. She then traveled to the frozen continent to conduct pioneering experiments that measured the accumulating chemicals there. “It’s very humbling now to be 30 years later and be able to say we have a clear fingerprint that the ozone hole is starting to get better,” she says.
Solomon says that public engagement was key to solving the ozone problem, with people coming together to identify an issue that threatened society and develop new technologies to fix it. In that respect, the most successful environmental treaty in history holds lessons for dealing with a much bigger threat, she says — climate change.
To fix the ozone layer, industry stopped using CFCs and similar compounds and replaced them with hydrofluorocarbons. Those chemicals, however, turned out to be powerful greenhouse gases that accelerated global warming. In October, the nations that ratified the Montreal Protocol agreed to expand it to cover hydrofluorocarbons as well (SN: 11/26/16, p. 13).
Some ants are so good at navigating they can do it backward.
Researchers think that foraging ants memorize scenes in front of them to find their way back to the nest. But that strategy only works when facing forward. Still, some species have been observed trekking in reverse to drag dinner home.
To find out how the ants manage this feat, Antoine Wystrach of the University of Edinburgh and colleagues captured foraging desert ants (Cataglyphis velox) near a nest outside Seville, Spain. In a series of tests, the researchers gave the ants cookie crumbles and then released the ants at a fork in the route back to their nest.
Regardless of which direction they took, ants walking backward with cookie bits in tow maintained a straight path. The researchers suspect the ants relied on some sort of sunlight cues. Ants also appeared to peek behind themselves to check and adjust course. After making adjustments, ants maintained their new direction no matter their body orientation. Desert ants combine their celestial compass and long-term visual memories of the route to find their way home, the team concludes online January 19 in Current Biology.
