Western Chimpanzee mum and daughter

Young chimpanzees in a West African forest form either trusting or independent ties with their mothers, but they do not display the confused, “disorganized” attachment style seen in many human children. 



That pattern, common among orphaned chimps raised by people, seems to be absent when animals grow up under natural survival pressures.



<h2 class="wp-block-heading" id="h-a-tale-of-two-attachment-styles"><a></a>A tale of two attachment styles</h2>



Field observers followed mother-infant pairs in Taï National Park, Côte d’Ivoire, for four years. They noted the parenting style of the chimpanzees. In particular, the experts studied how youngsters reacted when separated from or reunited with their mothers, and how boldly they explored.



Most fell into one of two familiar human categories. Some were secure: they checked in with their mothers during <a href="https://www.earth.com/news/stress-eats-away-our-brains-cognitive-defenses/" target="_blank" rel="noreferrer noopener">stress</a>, then ranged out with confidence.



Others showed insecure-avoidant attachment: they coped alone and rarely sought comfort. No infant behaved in the erratic, approach-and-retreat fashion that defines disorganized <a href="https://www.earth.com/news/the-way-you-send-emojis-shows-your-attachment-style/" target="_blank" rel="noreferrer noopener">attachment</a>.



According to attachment theory, secure bonds foster resilience, while insecure or disorganized ties can predict later anxiety or social trouble. In people, about one child in four shows the disorganized style.



Among captive, human-reared chimp orphans the rate soars to three out of five. The absence of that pattern in nature raises a striking possibility: the style may be maladaptive outside of sheltered environments.



<h2 class="wp-block-heading" id="h-parenting-style-of-wild-chimpanzees">Parenting style of wild chimpanzees </h2>



Disorganized attachment often follows trauma, fear, or unpredictable care. In forest life, any infant who hesitates at danger may expose itself to leopards, rival males, or territorial disputes. 



“In the wild, we found no evidence of disorganized attachment patterns among chimpanzees, which supports the hypothesis that this type of attachment may not be an adaptive survival strategy in the face of environmental constraints,” said first author Eléonore Rolland, a scientist at the <a href="http://www.isc.cnrs.fr/index.rvt" target="_blank" rel="noreferrer noopener">Institute of Cognitive Sciences Marc Jeannerod</a>.



If the response ever arises, its bearers probably fail to thrive or reproduce, erasing the trait from the visible population.



Captive <a href="https://www.earth.com/news/chimpanzees-share-alcoholic-fruit-to-increase-social-bonding/" target="_blank" rel="noreferrer noopener">chimpanzees</a>, by contrast, may live inside small enclosures, face no predators and rely on rotating human keepers. That unstable social mix can trigger the conflicted behaviors catalogued in laboratory tests. 



A parallel may exist for modern children who experience institutional care, high caregiver turnover, or chronic stress.



<h2 class="wp-block-heading" id="h-chimpanzee-lessons-for-parenting">Chimpanzee lessons for parenting</h2>



A deeper look at the findings nudges parents and policymakers to ask hard questions. “Our results deepen our understanding of chimpanzees' social development and show that humans and chimpanzees are not so different after all,” Rolland said.



“But they also make us think: have some modern human institutions or caregiving practices moved away from what is best for <a href="https://www.earth.com/news/five-scientifically-proven-steps-for-thriving-infant-development/" target="_blank" rel="noreferrer noopener">infant development</a>?”



Secure attachment in the forest emerged through steady proximity, gentle reassurance, and the freedom to explore within sight of the mother. Avoidant youngsters still stayed near but preferred self-soothing. Both strategies, the authors argue, work under natural constraints.



The third style appears only when normal mammalian care breaks down. If children in wealthy societies show that style at notable rates, the disruption may lie not in genetics but in caregiving routines: overstretched parents, frequent moves, rushed schedules, devices replacing touch.



<h2 class="wp-block-heading" id="h-chimpanzee-and-human-attachment">Chimpanzee and human attachment</h2>



“By identifying attachment patterns in wild chimpanzees, we provide important insights into the roots of human social behavior,” said senior author Roman Wittig from the <a href="https://www.eva.mpg.de/index/" target="_blank" rel="noreferrer noopener">Max Planck Institute for Evolutionary Anthropology</a>.



The work links psychology with field primatology and anthropology, tracing how early bonds shape adult society across species.



“Our findings suggest that shared attachment strategies in primates may reflect a common evolutionary heritage,” said co-author Catherine Crockford, a scientist at the same institute.



“The high prevalence of disorganized attachment in humans and captive orphan chimpanzees, in contrast to wild chimpanzees, also supports the idea that the rearing environment plays an important role in shaping attachment types.”



That insight underlines a long-standing debate. Are certain emotional disorders products of modern life rather than ancient biology? If wild primates, who share 98 percent of human DNA, avoid a pattern linked to later mood and relationship problems, then context - not species - may tip the scale.



<h2 class="wp-block-heading" id="h-conservation-and-child-welfare">Conservation and child welfare</h2>



Protecting chimpanzee habitats does more than save a charismatic animal; it preserves the social conditions that allow normal attachment to flourish. 



Orphan rescue centers might adjust caregiving protocols to reduce inconsistency and replicate maternal security rather than relying on multiple human feeders.



In the human realm, the research supports policies that stabilize early care: parental leave, low child-to-caregiver ratios, trauma-informed schooling.



<h2 class="wp-block-heading" id="h-chimpanzee-parenting-next-steps">Chimpanzee parenting: Next steps</h2>



The Taï study followed infants until weaning, around age four to five. Future projects could test whether early attachment style predicts later rank, alliance skills, or parenting success.



Researchers also plan to compare <a href="https://www.earth.com/news/bonobos-group-cohesion-common-enemy-effect-do-not-kill-inside-their-species/" target="_blank" rel="noreferrer noopener">bonobos</a>, whose matriarchal societies differ from chimpanzees, and to track hormone levels that might signal stress during separations. 



At the same time, developmental psychologists may revisit human data from cultures with extended family caregiving or from hunter-gatherer groups that mirror ancestral conditions.



If disorganized attachment drops in those settings, it would strengthen the case that modern disruptions - not innate tendencies - fuel the pattern.



<h2 class="wp-block-heading" id="h-trust-risk-and-survival">Trust, risk, and survival</h2>



In the forest canopy, a mother chimp pauses, her infant scrambling over branches before returning to her side. The scene looks simple, yet it echoes deep principles about trust, risk and survival.



By watching our closest relatives, scientists remind us that the first ties we form still guide us decades later - and that nurturing those ties may be one of the most ancient, and vital, tasks any society undertakes.



The study is published in the journal <a href="https://www.nature.com/articles/s41562-025-02176-8" target="_blank" rel="noreferrer noopener">Nature Human Behavior</a>.



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What wild chimpanzees can teach us about parenting

Young chimpanzees in a West African forest form either trusting or independent ties with their mothers, but they do not display the confused, “disorganized” attachment style seen in many human children. That pattern, common among orphaned chimps raised by people, seems to be absent when animals grow up under natural survival pressures. A tale of two attachment styles Field observers followed mother-infant pairs in Taï National Park, Côte d’Ivoire, for four years. They noted the parenting style of the chimpanzees. In particular, the experts studied how youngsters...

Mammals have a pharynx, or throat, that starts at the back of the nose and ends below the back of the mouth. Although the pharynx is a single tube, it leads into two separate tubes - the windpipe, through which air reaches the lungs, and the esophagus, through which food reaches the <a href="https://www.earth.com/news/lizard-preserved-stomach-microraptor/">stomach</a>. The separation of the respiratory and digestive tracts at the base of the pharynx is critical for survival; air must be directed from the pharynx into the lungs, but food must be directed towards the stomach and must not enter the lungs.



This anatomical arrangement presents problems for mammals, who must avoid inhaling their food when they try to swallow it. This is the cause of choking and can be fatal. The situation is even more complicated for baleen whales, which feed while underwater. They open their mouths wide and lunge through a shoal of fish or small invertebrates, taking in numerous small prey items along with thousands of liters of water that must not flow into the windpipe.



Researchers at the <a href="https://www.ubc.ca/">University of British Colombia</a> in Vancouver have recently published a study that shows how baleen whales, also known as rorquals, achieve the separation of respiratory and digestive tracts while their mouths experience these extreme physical forces. They identified an anatomical mechanism that protects the whale’s airway as tons of water gushes into its mouth - they term this bulbous region of the soft palate the “oral plug.”



“We discovered a structure in fin whales, which likely exists in all lunge-feeding whales, or rorquals,” said Kelsey Gil of the UBC Zoology Department. “We’ve termed it the ‘oral plug’ and found that it blocks the channel between mouth and pharynx. It means that when a whale lunges, the entrance to the pharynx and thus the respiratory tract is protected.”



Although the mechanics of lunge feeding by whales was well understood, not much was known about how prey such as krill are manipulated and swallowed after a lunge. In addition, the general anatomy of the larynx was also well known. This is a hollow organ in the upper airway that is also the location of the vocal cords and has been investigated in connection with whale vocalizations. However, not much was known about the structure of the rest of the pharynx, the critical junction between respiratory and digestive tracts.&nbsp;



“It’s impossible to study this in a living whale, so we rely on tissue from deceased whales and use functional morphology to assess the relationship between a structure and its function,” said Gil.&nbsp;



By examining and dissecting adult and fetal fin whales, the researchers found that a musculo-fatty structure, the oral plug, seals the back of the mouth and pharynx when the whales feed. They manipulated the various structures to see how they could move. They also looked at the direction of muscle fibers to understand how they would move when muscles contracted and shortened.



“The oral plug is a part of the soft palate, so simply considering the gross anatomy, there is only one direction it should move,” explained Gil. “When the oral plug moves backward and upward to block the nasal cavities, it means that no other structure can be in that same spot below the nasal cavities. This forced us to then examine the larynx, since that spot is where we would expect to see the larynx during breathing, but it cannot be in that position during swallowing.”



During swallowing, the oral plug is lifted and this allows food to pass from the mouth into the pharynx. At the same time, the lifted plug protects the upper airways from food entry. The larynx is positioned at the floor of the pharynx, where laryngeal cartilages close to protect it. A muscular sac attached to the bottom of the larynx is forced upwards into the laryngeal cavity to completely block the lower respiratory tract.



The findings, published in the journal <a href="https://www.cell.com/current-biology/home">Current Biology</a>, also show that the pharynx in fin whales - and likely all rorquals - can only be used by either the respiratory or the digestive tract at any one time. This protects the animals from choking while feeding.&nbsp;



According to the researchers, no structure like the oral plug has been reported in any other animals. “There are very few animals with lungs that feed by engulfing prey and water, so the oral plug is likely a protective structure specific to rorquals that is necessary to enable lunge feeding,” said Gil.



The study authors conclude that these adaptations to facilitate swallowing in lunge-feeding whales were a critical development in the evolution of large body size. The largest animal species ever to have lived is thought to be the blue whale, which feeds in precisely this way.



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By <a href="mailto:bosman@truewan.co.za">Alison Bosman</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

"Oral plug" prevents whales from drowning while they eat

Mammals have a pharynx, or throat, that starts at the...

When a breeder of tarantulas noticed, in 2018, that several of his spiders were becoming sick and dying, he approached parasitologist Adler Dillman from the <a href="https://www.ucr.edu/">University of California, Riverside</a>. The ailing tarantulas were characterized by what appeared to be a white discharge in and around the oral cavity. On closer inspection, however, it became clear that the white mass was a large infestation of nematode <a href="https://www.earth.com/news/worms-without-ears-can-hear-through-their-skin/">worms</a> intertwined together inside and around the spider’s mouth.&nbsp;



Dillman and his colleagues examined the worms and, based on a combination of morphological and morphometrical data, and unique DNA sequences, they identified a new species of nematodes. There are more than 25,000 different species of nematode worms and they are among the most abundant animals on Earth. They parasitize a wide range of living organisms, but this is only the second time that a species has been found to infect tarantulas.



The scientists named the new species Tarantobelus jeffdanielsi, after Jeff Daniels, the American actor, musician and producer. They named it in Daniels’ honor because his character in the 1990 film ‘Arachnophobia’ saves a town from a deadly infestation of spiders.&nbsp;



“His character in the film is a spider killer, which is exactly what these nematodes are,” said Dillman, who led the team that discovered the nematode.



“When I first heard a new species of nematode had been named after me, I thought, ‘Why? Is there a resemblance?’” joked Daniels. “Honestly, I was honored by their homage to me and 'Arachnophobia.' Made me smile. And of course, in Hollywood, you haven’t really made it until you’ve been recognized by those in the field of parasitology.”



The scientists investigated the lifecycle of the worms, and where exactly they resided in the infected spiders. They found that infestations of worms occurred in the mouth area and on the pedipalps, special appendages near the mouth that the spiders use to sense and manipulate food. No worms were found in the stomachs of infected spiders.&nbsp;



Once infected, spiders lost the ability to use their jaws and feed themselves, and began to show strange behavior, such as walking on the very tips of their legs. The infection would ultimately prove fatal for a tarantula, as it would starve to death.&nbsp;



“It may take months because tarantulas don’t have to eat particularly often. However, if they get this infection, they will die of starvation,” Dillman said.&nbsp;



When culturing the nematode worms in the laboratory, the researchers noted that they ate bacteria such as E. coli and did not appear to feed off the parasitized spiders themselves. This led the researchers to conclude that the worms may be feeding on the bacteria found around the oral cavity of the spider.&nbsp;



However, there is not yet an understanding of how the worms change tarantula behavior or render the pedipalps and jaws non-functional. Dillman is planning additional studies to investigate this, as well as how breeders can treat or even prevent infections in their captive-bred tarantulas.



The researchers found that the average lifespan of jeffdanielsi nematodes in the laboratory was 11 days. These worms are mostly hermaphrodites – each individual produces sperm as well as eggs. Furthermore, they fertilize themselves and each produces approximately 160 offspring within its 11-day lifespan.



Although this is only the second time that nematode parasites have been found infecting tarantulas, Dillman feels this reflects the fact that little research is done on these spiders. Nematode worms are very common parasites and it would be unusual if there were no species that parasitized tarantulas.



“Nematodes have been around for hundreds of millions of years. They’ve evolved to infect every kind of host on the planet including humans,” he said. “Any animal you know of on planet Earth, there’s a nematode that can infect it.”



The team’s work describing jeffdanielsi has recently been&nbsp;<a href="https://meridian.allenpress.com/journal-of-parasitology/article-abstract/108/1/30/476785/TARANTOBELUS-JEFFDANIELSI-N-SP-PANAGROLAIMOMORPHA?redirectedFrom=fulltext">published</a>&nbsp;in the&nbsp;<a href="https://meridian.allenpress.com/journal-of-parasitology">Journal of Parasitology</a>.



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By <a href="mailto:bosman@truewan.co.za">Alison Bosman</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Scientists have discovered worms that kill tarantulas

When a breeder of tarantulas noticed, in 2018, that several...

Protecting 30 percent of land and <a href="https://www.earth.com/news/ocean-heat-reached-a-record-high-for-the-sixth-straight-year/">sea</a> by 2030 is an important benchmark, but it will not be enough to halt and reverse biodiversity loss, according to a team of more than 50 scientists from 23 countries. 



The experts delivered a synthesis of the science supporting 21 targets in a draft of the <a href="https://www.cbd.int/article/draft-1-global-biodiversity-framework">Post-2020 Biodiversity Framework</a>, a plan being negotiated by the United Nations.



The scientists are calling for systematic changes, including substantial reductions in damaging fisheries and farming subsidies, great reductions in overconsumption, and limiting global warming to 1.5°C.&nbsp;



Paul Leadley, a professor at Paris-Saclay University, is also an assessment leader and past chair of <a href="http://www.biodiscovery.com/">BioDISCOVERY</a>.



“The target of protecting 30% of all land and seas is important and attracting a lot of attention. And expanding protected areas is a good start if done well, but far short of what's needed to halt and reverse biodiversity loss - called ‘bending the curve’ for biodiversity."



"There’s very good evidence that we will fail again to meet ambitious international biodiversity objectives if there’s too much focus on protected areas at the expense of other urgent actions addressing the threats to biodiversity.”&nbsp;



“Governments are clearly struggling with the breadth and depth of the ‘transformative changes’ needed to bend the curve for biodiversity, and sometimes seem unwilling to face up to it.&nbsp; But deep changes are necessary and will greatly benefit people in the long run.”



The key points highlighted in the study were that reversing biodiversity loss requires transformative change, coordinated at every level. Along with these changes, assessments must be carried out and greater monitoring efforts funded. Perhaps most importantly, action must be taken immediately to be impactful.&nbsp;



“The sooner we act the better. Time lags between action and positive outcomes for biodiversity can take decades so we must act immediately and sustain our efforts if we are to reach the global goals by 2050," said study co-author Maria Cecilia Londoño Murcia of the Humboldt Institute.



"The time needed for safeguarding and restoring ecosystem structure, function and resilience is particularly critical for people and communities whose livelihoods and well-being directly depend on these systems and the benefits they provide.”&nbsp;



---By <a href="mailto:zachfitzner@yahoo.com">Zach Fitzner</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Sweeping changes needed to reverse biodiversity loss

Protecting 30 percent of land and sea by 2030 is...

Insects don’t have noses and are not able to “smell” the roses in the familiar sense of the word. Instead, most odor molecules are detected by chemoreceptors that occur on an insect’s antennae. Using these chemical receptors, insects are capable of perceiving and differentiating between thousands of&nbsp;airborne compounds. They use these chemical signals to locate forage <a href="https://www.earth.com/news/some-plants-wont-survive-the-loss-of-seed-dispersing-animals/">plants</a> and mates, as well as to avoid predators.



But now, new research indicates that common air pollutants present in rural and urban environments may be hampering the ability of insects to detect the chemical signals so crucial to their activity as pollinators.&nbsp;



A team of scientists from the <a href="http://www.reading.ac.uk/">University of Reading</a> has conducted the first study to observe that common air pollutants, including diesel exhaust fumes and ozone, have a negative impact on the success of pollination by insects.&nbsp;



“We knew from our previous lab studies that diesel exhaust can have negative effects on insect pollinators, but the impacts we found in the field were much more dramatic than we had expected," said Dr. Robbie Girling, who led the project.



These previous laboratory studies by members of the Reading team showed that&nbsp;chemicals in <a href="https://www.reading.ac.uk/news-archive/press-releases/pr649662.html">diesel fumes react with and can change the scents of flowers such that the insects cannot locate the flowers. </a>The research suggested that pollution could contribute to the ongoing declines in pollinating insects, by making it harder for them to locate the pollen and nectar that form their food.



In the new study, the researchers aimed to gather evidence showing how air pollution affects different species of pollinating insects, some of which rely on scent more heavily than others.



The study, funded by the Natural Environment Research Council, used a purpose-built fumigation facility to regulate levels of nitrogen oxides (NOx) – present in diesel exhaust fumes – and ozone in an open field environment. They then observed the effects these pollutants had on the pollination of black mustard plants by free-flying, locally-occurring pollinating insects over the course of two summer field seasons.



Although the experiments made use of pollution levels that were way below the maximum acceptable levels considered as safe in the US, the results of the field experiments were dramatic. The researchers observed 62 to 70 percent fewer pollinator visits to the plants located in polluted air. This reduction was seen in seven different groups of pollinators, including bees, moths, hoverflies and butterflies.&nbsp;



There were also 83 to 90 percent fewer visits to flowers by these insects, and ultimately a 14 to 31 percent reduction in pollination success, based on the measurement of seed yield and other factors.



“The findings are worrying because these pollutants are commonly found in the air many of us breathe every day," said Dr. James Ryalls. "We know that these pollutants are bad for our health, and the significant reductions we saw in pollinator numbers and activity shows that there are also clear implications for the natural ecosystems we depend on.”



Insects are important pollinators of crops upon which we depend for food and so a reduction in pollinating activity could have far-reaching economic and social consequences. Around 70 percent of crop species rely on insects for pollination; these include apples, strawberries and cocoa.&nbsp;



In addition, pollination supports around eight percent of the total value of agricultural food production, worldwide. The pollinating activity of insects thus generates hundreds of billions of pounds worth of economic value each year.&nbsp;



Furthermore, far higher levels of air pollutants are found in many areas around the world where people and businesses breach the regulations. For example, a&nbsp;<a href="https://www.independent.co.uk/climate-change/news/air-pollution-england-defra-labour-who-nitrogen-dioxide-luke-pollard-b404484.html?r=55147">2019 analysis</a> recorded illegal levels of nitrogen dioxide present in local authorities, in large areas of northern England (including Cheshire and Gateshead), and in southern England (including Wiltshire, Chichester and rural areas such as the New Forest).



“This truly cross-disciplinary work demonstrated very clearly how atmospheric pollutants negatively impact on pollination with direct consequences for food production as well as the resilience of our natural environment," concluded study co-author Dr. Christian Pfrang.



Their results are published today in the <a href="https://doi.org/10.1016/j.envpol.2022.118847">&nbsp;journal&nbsp;</a><a href="https://www.journals.elsevier.com/environmental-pollution">Environmental Pollution</a>.



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By <a href="mailto:bosman@truewan.co.za">Alison Bosman</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Air pollutants confuse pollinators and reduce food production

Insects don’t have noses and are not able to “smell”...

In a new study from <a href="https://wsu.edu/">Washington State University</a> (WSU), experts have found that a high protein diet increases the risk of kidney <a href="https://www.earth.com/news/coffee-stimulates-digestion-and-protects-against-disease/">disease</a> and premature death among captive polar bears. 



Previous studies have suggested that there is a similar link between kidney disease and excessive protein consumption among humans. The Mayo Clinic reports that a high-protein diet may worsen kidney function in humans, particularly in the long term, because the body may struggle to eliminate all the waste products.



A research team led by WSU wildlife biologist Charlie Robbins investigated what zoos have typically been feeding polar bears. The study revealed that their diet usually consists of a food ratio intended for big cats, containing about two to three parts protein to one part fat. This diet is the opposite of what polar bears would be eating in the wild.&nbsp;



“Zoos made some assumptions in the past about the nutritional requirements of polar bears because their diet is almost exclusively animals,” said Professor Robbins. “But, unlike cats, they do not need and cannot tolerate high protein.”



Even though polar bears are carnivores that feed mainly on seals, researchers have found that they have physiology that is more closely aligned with humans and other omnivores.



Looking at death records of captive polar bears, the researchers discovered that the most common cause of death was kidney disease. Bears with fatal kidney disease died 10 years earlier than bears without the condition. The second most common causes of death were liver disease and cancer, according to the analysis.&nbsp;&nbsp;



Out of more than 600 bears examined in the wild, the team found no evidence kidney disease.



“A slate of early deaths across sexes that is limited to two major organs raised several red flags for us,” said Professor Robbins, who has researched both grizzly and polar bear nutrition for more than 35 years.



Former WSU graduate student Karyn Rode conducted field studies which showed that wild polar bears prefer a diet that is two parts fat to one part protein.



“Although we knew that polar bears selected for the blubber of their prey, this was the first time we were able to quantify how much fat they were actually consuming,” said Professor Robbins. “When it comes to feeding polar bears, the general mindset has been that they are carnivores. No one has really been paying attention to the amount of protein they might need, much less limitations on how much they might tolerate.”



In the current paper, the researchers propose that - like humans - both polar and grizzly bears require relatively low levels of protein. When captive bears were offered their choice of blocks made up of pure lard and blocks made up of high protein meat, they ultimately consumed the same ratio of fat to protein as their relatives in the wild.



The study authors recommend that zoos should adopt alternative foods for captive polar bears that mimic the fat-protein ratio found naturally in the wild. Once these alternatives are introduced, monitoring the animals could help experts determine whether the new diets may improve their health and longevity.



The study is published in the journal <a href="https://onlinelibrary.wiley.com/journal/10982361">Zoo Biology</a>.



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By <a href="http://csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

High protein diet causes kidney disease in polar bears

In a new study from Washington State University (WSU), experts...

There are a few species of beetles that can jump, but beetle larvae tend to squirm across the substratum and have never been seen doing acrobatic jumps -- until now.



A team of researchers has published a scientific article documenting the jumping behavior of larval lined flat bark beetles (Laemophloeus biguttatus). This type of <a href="https://www.earth.com/news/animal-locomotion-natural-energy/">locomotion</a> has not been recorded for beetle larvae before. 



The larvae are able to spring into the air with a speed of around 0.5 meters per second, and to travel forwards a distance approximately equivalent to four times their own body length. While flying through the air, the larva curls itself into a loop and as it lands, it bounces and rolls along until it becomes stationary.&nbsp;



“Jumping at all is exceedingly rare in the larvae of beetle species, and the mechanism they use to execute their leaps is – as far as we can tell – previously unrecorded in any insect larvae,” said study co-author Matt Bertone, director of <a href="https://www.ncsu.edu/">North Carolina State University</a>’s Plant Disease and Insect Clinic.&nbsp;



“The way these larvae were jumping was impressive at first, but we didn’t immediately understand how unique it was,” said Bertone. “We then shared it with a number of beetle experts around the country, and none of them had seen the jumping behavior before. That’s when we realized we needed to take a closer look at just how the larvae was doing what it was doing.”



Usually when insects make impressive jumps, they rely on a “latch-mediated spring actuation mechanism.” This means that two parts of the body latch onto each other while the insect exerts force using its muscles. When this builds up a significant amount of potential energy, the insect unlatches the two parts and all the stored energy is released at once. This results in an action-packed spring off the ground.



The researchers looked for a two-part latch mechanism on the surface of the lined flat bark beetle larvae and found nothing. Then, they used microCT scans to measure how much muscle the beetle larvae had and calculated whether this would provide enough power to launch the larvae into the air at a speed of 0.5 meters per second. The larvae did not have enough muscle to achieve this by muscle action alone.&nbsp;



The conclusion was that the larvae must be using some form of spring-loaded system to achieve their acrobatic jumps. This is when Bertone and study co-author Adrian Smith decided to film the behavior in order to get a better understanding of what was taking place. Smith is a research assistant professor of biological sciences at NC State and head of the Evolutionary Biology &amp; Behavior Research Lab at the North Carolina Museum of Natural Sciences.



The team filmed some jumps at 60,000 frames per second and were able to see that the beetle larvae actually hook their feet into the ground as they arch their bodies and prepare to jump. As soon as one foot loses its grip on the ground, the spring is released and the larva is propelled into the air under the power of its body’s own potential energy store.



“What makes the&nbsp;L. biguttatus&nbsp;so remarkable is that it makes these leaps without latching two parts of its body together,” said Bertone. “Instead, it uses claws on its legs to grip the ground while it builds up that potential energy – and once those claws release their hold on the ground, that potential energy is converted into kinetic energy, launching it skyward.”



Meanwhile, in&nbsp;<a href="https://www.youtube.com/watch?v=SEst5RERHJ4">an unrelated video about jumping maggots</a>, Smith had included a short clip of the jumping behavior in&nbsp;L. biguttatus. That video was seen by Takahiro Yoshida, a researcher from Tokyo Metropolitan University in Japan, who had witnessed similar jumps in the larvae of another beetle species called&nbsp;Placonotus testaceus, but had not published anything related to the behavior. Yoshida is a co-author on the publication about this unusual form of locomotion.



“We don’t have high-speed footage of&nbsp;P. testaceus, but the video evidence we do have from Yoshida’s lab suggests that this previously unknown behavior is found in two different genera which are not even closely related,” said Bertone.



“This raises a lot of questions. Has this behavior evolved separately? Is it found in other beetle species? Are these genera more closely related than we previously suspected? There’s a lot of interesting work to be done here.”



Details of this unusual method of locomotion in lined flat bark beetle larvae are published today in the journal <a href="https://journals.plos.org/plosone/">PLOS ONE</a>.



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By <a href="mailto:bosman@truewan.co.za">Alison Bosman</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Unusual jumping behavior recorded in beetle larvae

There are a few species of beetles that can jump,...

A new study from the <a href="https://www.ubc.ca/">University of British Columbia</a> has revealed that 45 percent of the fish that cross through two or more exclusive economic zones (EEZs) will shift their movement patterns by 2100. This is expected to possibly bring international conflict.&nbsp;



By 2030, 23 percent of these fish are predicted to change their historic ranges. By 2100, this increases to 45 percent of the transnational fish, along with 81 percent of EEZs seeing at least one species shift. The culprit for these changes is, of course, human-caused climate change.&nbsp;&nbsp;&nbsp;&nbsp;



“This is not only an issue of stocks leaving or arriving to new EEZs, but of stocks that are shared between countries, completely changing their dynamics,” said study lead author Dr. Juliano Palacios-Abrantes, who conducted the study while at UBC’s Institute for the Oceans and Fisheries (IOF).&nbsp;



“We will see even more dramatic changes by 2030 and onwards, given current emissions rates. Many of the fisheries management agreements made to regulate shared stocks were established in past decades, with rules that apply to a world situation that is not the same as today.”



The researchers tracked the changing ranges of 9,132 transnational fish populations, which account for 80 percent of the catch from the world's exclusive economic zones. The research started in 2006 and continued forward with projections predicted up to 2100.&nbsp;&nbsp;



“By providing estimates of the size and timing of projected shifts, our study offers tangible reference points around which to consider climate change impacts and negotiate fair policies for sustainable management” said study co-author Dr. Colette Wabnitz, lead scientist at Stanford’s Center for Ocean Solutions.



“We must accept that climate change is happening, and then move fast enough to adapt fisheries management regulations to account for it,” said co-author Dr. Gabriel Reygondeau, a research associate at IOF.



The scientists hope their study can create a framework for international negotiations and planning to create a well designed fisheries management plan for the future. Without this, conflict, even violent conflict could arise over dwindling fish populations supporting a hungry human populace.&nbsp;



The study is published in the journal <a href="https://onlinelibrary.wiley.com/journal/13652486">Global Change Biology</a>.&nbsp;



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By <a href="mailto:zachfitzner@yahoo.com">Zach Fitzner</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Nearly half of the world’s shared fish are on the move

A new study from the University of British Columbia has...

A new study published in the journal <a href="https://www.pnas.org/content/119/2/e2023340118">Proceedings of the National Academy of Sciences</a> has found that the mechanisms behind the sense of <a href="https://www.earth.com/news/how-can-a-smell-transport-us-to-another-place/">smell</a> may be far simpler than previously thought. By studying the olfactory sense of locusts, a research team led by the <a href="https://wustl.edu/">Washington University in St. Louis</a> mapped the neuronal underpinnings behind invariant odor recognition.



“The smell of coffee is the same whether it is smelled in a coffee shop or grocery shop (different backgrounds), on a hot day or a cold day (different ambient conditions), after lunch or dinner (different temporal contexts), or using a deep inhalation or normal inhalation (different stimulus dynamics),” explained the study authors.



“This feat of pattern recognition that is still difficult to achieve in artificial chemical sensing systems is performed by most sensory systems for their survival. How is this capability achieved?”



In order to answer this question, the scientists first trained locusts to associate a specific odor with some of their favorite foods, such as blades of grass. After staying without food for a day, the locusts were exposed to a puff of odor (hexanol or isoamyl acetate), then given a blade of grass. After only six such presentations, the locusts learned to open their palps (the sensory appendages close to its mouth) in expectation of food immediately after smelling the “training odorant.”



The researchers then mapped which neurons were activated when the locusts were exposed to the odorant under different environmental conditions, such as in conjunction to other smells, in humid or dry conditions, or when the locusts were fully fed or starving. Even though the locusts opened their palps every time, different patterns of neurons were activated, depending upon each specific context.



"The neural responses were highly variable," said study senior author Baranidharan Raman, a professor of Biomedical Engineering at Washington University. "That seemed to be at odds with what the locusts were doing, behaviorally."



To understand how variable neural responses produced stable behavior, Professor Raman and his colleagues used a machine-learning algorithm that exploited two functional types of neurons: “ON neurons,” which were activated when an odorant was present, and “OFF neurons,” which fired only after the odor presentation had ended.&nbsp;



"You can think of the ON neurons as conveying 'evidence for' an odor being present, and OFF neurons as 'evidence against' that odor being present," explained Professor Raman.&nbsp;



To recognize the presence of an odorant, the scientists simply needed to add evidence for the odorant being present (add the spikes across all ON neurons), and subtract evidence against the odorant being present (add the spikes across all OFF neurons). If the result was above a certain threshold, the machine learning algorithm would reliably predict that the locust smelled the odor and opened its palps.



“We were surprised to find that this simple approach is all that was needed to robustly recognize an odorant,” Professor Raman concluded.



---



By <a href="mailto:andrei.ionescu5891@gmail.com">Andrei Ionescu</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer&nbsp;&nbsp;

Locusts have a surprisingly simple way of sensing smells

A new study published in the journal Proceedings of the...

Observing animal <a href="https://www.earth.com/news/ocean-acidification-disrupts-the-behavior-of-fish-shoals/">behavior</a> and ecology in the wild is the basis of conservation planning. However, the cost, time commitment, and danger involved in basic observational work can make it extremely challenging.&nbsp;



Scientists often substitute observations with data collected through biologging devices. These high-tech devices can monitor heart rate, breathing, animal movement, and more. To accurately interpret data from logging devices, statistical analysis is needed. Like other scientific technologies, statistical tools are always evolving. A new study from the <a href="https://www.ubc.ca/">University of British Columbia</a> improves on statistical tools used for interpreting data from biologgers.&nbsp;&nbsp;



“The thing we really tackled with this paper was trying to get at some of those fine-scale behaviors that aren’t that easy to model,” said study lead author Evan Sidrow, a doctoral student in the UBC Department of Statistics.&nbsp;



“It’s a matter of finding behaviors on the order of seconds - maybe 10 to 15 seconds. Usually, it’s a matter of a whale looking around, and then actively swimming for a second to get over to a new location. We are trying to observe fleeting behaviors, like a whale catching a fish.”



The researchers improved a statistical tool based on a hidden Markov model, which is used to interpret animal movement datasets.



“Traditional hidden Markov models break down at very fine scales,” said Sidrow. “That’s because there’s structure in the data you can’t capture using the basic type of hidden Markov model. We’re trying to capture it with this model - we’re trying to account for this ‘wigglyness' that a traditional hidden Markov model wouldn’t be able to account for.”



Because modern data logging devices collect data almost continuously, an enormous amount of data points are collected in a relatively short period of time. The Markov model has a hard time interpreting such a large amount of data. The new statistical modeling method allows a finer scale look into the data, which produces greater information for conservation planning by decision makers, including those working on orca conservation.&nbsp;&nbsp;



"As a case study, we use this framework to model the fine-scale kinematic movements of a northern resident killer whale ( Orcinus orca) off the western coast of Canada," wrote the study authors.&nbsp; "Through simulations, we show that our model produces more interpretable state estimation and more accurate parameter estimates compared to existing methods."



According to study senior author Dr. Marie Auger-Méthé, the study is one of the first steps on the road to fully understanding why southern resident killer whales are not faring as well as their northern counterparts.



“Using our methods to detect when the animals are catching prey and to model their energy expenditure will be key to understanding the differences between these neighbouring whale populations,” said Dr. Auger-Méthé.



She explained that the next goal is to understand when the whales are capturing prey and applying the models to both northern and southern resident killer whale populations to see how they are behaving differently.



“The paper offers many ‘building block’ solutions that can be used together or independently,” said Dr. Auger-Méthé. “In essence, we are providing a toolbox to researchers using high-frequency movement data, and other similar high-frequency time series.”



The study is published in <a href="https://onlinelibrary.wiley.com/journal/1708945x">The Canadian Journal of Statistics</a>.



---



By <a href="mailto:zachfitzner@yahoo.com">Zach Fitzner</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

New statistical tool could improve killer whale conservation

Observing animal behavior and ecology in the wild is the...

Mammals in general are not able to digest cellulose, the carbohydrate that is found in the cell walls of plant cells. Even <a href="https://www.earth.com/news/large-herbivores-must-be-restored-to-balance-ecosystems/">herbivores</a>, such as cows, horses and elephants do not produce the enzyme that breaks down cellulose. Instead, mammals (including humans) need gut microbes to carry out this function and enable them to access the nutrients found inside plant cells.&nbsp;



Giant pandas (Ailuropoda melanoleuca) are unusual because they are bears, in the order Carnivora, but their diet consists entirely of bamboo leaves and shoots. Carnivores have short gastrointestinal tracts, geared for digesting animal flesh, and this makes the herbivorous diet of giant pandas even harder to process efficiently. Pandas are thus heavily dependent on the microbes in their guts for breaking down cells in leaves and shoots to make the contents available.



In the wild, pandas feed on fibrous old bamboo leaves for eight months of the year. This diet is poor in nutrients and contains almost no fat. However, during late spring and early summer the bears feed on new shoots that have a higher nutritional value that enables them to gain weight.&nbsp;



Previous research has shown that the gut microbiome of giant pandas changes between the leaf-eating season and the shoot-eating season. However, there has been no research on the effects of these seasonal changes on the body characteristics or physiology of the pandas.&nbsp;



A study published today in the journal&nbsp;<a href="https://www.cell.com/cell-reports/home">Cell Reports</a> addresses this gap in current understanding and finds that shifts in the gut microbes enable pandas to gain weight and store fat when bamboo shoots are available to eat.&nbsp;



“This is the first time we established a causal relationship between a panda’s gut microbiota and its phenotype,” said study first author Guangping Huang from the <a href="https://english.cas.cn/">Chinese Academy of Sciences</a>. “We’ve known these pandas have a different set of gut microbiota during the shoot-eating season for a long time, and it’s very obvious that they are chubbier during this time of the year.”



The team of scientists, led by Fuwen Wei at the CAS Institute of Zoology, has been studying wild giant pandas living in the Qinling Mountains in central China for decades. The team collected fecal samples from eight adult pandas during the leaf-eating season (14 samples) and the shoot-eating season (15 samples). These were assessed for the presence and numbers of different types of gut microbes.&nbsp;



Wei says that these wild pandas have distinctly different populations of gut bacteria in the two seasons. In particular, a significantly higher abundance of a bacterium called&nbsp;Clostridium butyricum&nbsp;is present in the gut during the shoot-eating season compared with during the leaf-eating season. Gas chromatography-mass spectrometry of the short-chain fatty acids in the feces also revealed that the fatty acids butyrate and acetate were present in greater amounts during shoot-eating season.



Although bamboo leaves and shoots contain almost no fat, pandas were able to gain weight and store fat when they preferentially ate shoots. The bacterium C. butyricum produces the fatty acid butyrate as a product of its metabolism in the gut of the pandas, and the scientists were interested in the effects of this fatty acid on panda metabolism.



To investigate whether the change in gut microbiota could affect a panda’s metabolism, the researchers performed a fecal transplant of panda feces, collected in the wild, to the intestinal tracts of germ-free mice. They introduced fecal matter from panda donors during the leaf-eating season into some mice, while other mice received feces collected from pandas during the shoot-eating season. A third group of mice – the control group – received no panda fecal matter.&nbsp; Then they fed the mice for 3 weeks with a bamboo-based diet that simulated what pandas eat. &nbsp;



The experts found that mice transplanted with panda feces collected during shoot-eating season gained significantly more weight and had more fat after 21 days than mice transplanted with feces from leaf-eating season, despite consuming the same amount of food. Further analysis revealed that the fatty acid butyrate, a metabolic product of&nbsp;C. butyricum, could upregulate (enhance) the expression of a gene called&nbsp;Per2, which increases lipid synthesis and storage. Thus, the mice showed the same patterns of seasonal weight gain as the pandas do, indicating the critical role of the gut microbiome in panda metabolism.



Fat storage is important in many animals that eat a nutrient-poor diet. The bamboo eaten by pandas in the wild is deficient in fat but the shoots, eaten in late spring and early summer, contain higher levels of protein and carbohydrate. The gut bacteria in these mammals enables them to use the protein and additional carbohydrates in the shoots, to synthesize lipids that are then available for storage.&nbsp;



Many animals experience a seasonal shift in gut bacteria as a result of changes in food availability. For example, certain species of monkeys have different gut microbiota in summer, when they eat fresh leaves and fruits, compared with that in winter, when they feed on leaves and tree bark. A similar shift has also been observed in the digestive systems of Hadza people, modern hunter-gatherers living in Tanzania, as the type of available food changes through the year.



The researchers plan to investigate and map out more microorganisms in the panda’s gut in future, and to find out how they affect the animals’ health. “Causal research of host phenotype and gut microbiota in wild animals is just beginning. Identifying what bacteria are beneficial for animals is very important, because one day we may be able to treat some diseases with probiotics,” said Huang.



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By <a href="mailto:bosman@truewan.co.za">Alison Bosman</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Giant pandas’ gut bacteria turn nutrient-poor food into fat

Mammals in general are not able to digest cellulose, the...

The turning blades on wind turbines and drones make a <a href="https://www.earth.com/news/traffic-noise-linked-to-higher-risk-of-dementia/">noise</a>, as do the airfoils used on planes and helicopters. Most of the nose that arises as an object moves through air originates at the trailing edge as air flowing over and under the object meet. The same is true for the noise that a bird’s wings make as it flies overhead – except, of course, in the case of owls. They are renowned for being able to fly silently.



In&nbsp;a quest to design airfoils that produce less noise pollution, researchers from <a href="http://en.xjtu.edu.cn/">Xi'an Jiaotong University</a> mimicked the characteristics of owl wings to inform a new design of airfoil that significantly reduces the trailing-edge noise. Details of the study are published today in the journal <a href="https://aip.scitation.org/journal/phf">Physics of Fluids</a>.



“Nocturnal owls produce about 18 decibels less noise than other birds at similar flight speeds due to their unique wing configuration,” said study co-author Xiaomin Liu. “Moreover, when the owl catches prey, the shape of the wings is also constantly changing, so the study of the wing edge configuration during owl flight is of great significance.”



When air flows over the top of an airfoil-shaped surface, it forms a layer of turbulence. Similarly, air flowing underneath also forms a layer of turbulence, and these two layers meet at the trailing edge of the structure. When they meet and air flows back through the trailing edge, it scatters and radiates noise.&nbsp;



The wing feathers of owls form a serrated edge at the trailing end of the wing, and this is thought to minimize turbulence and the associated noise. Previous studies have explored the use of serrated trailing edges and found that the serrations effectively reduce the noise of rotating airfoils. However, the noise reduction was not universal, depending heavily on the way in which the airfoil was used.



“At present, the blade design of rotating turbomachinery has gradually matured, but the noise reduction technology is still at a bottleneck,” said Liu. “The noise reduction capabilities of conventional sawtooth structures are limited, and some new non-smooth trailing-edge structures need to be proposed and developed to further tap the potential of bionic noise reduction."



The researchers used noise calculation and analysis software to conduct a series of detailed theoretical studies of simplified airfoils that had characteristics reminiscent of owl wings. They applied their findings to suppress the noise of rotating machinery.



The study showed that improving flow conditions around the trailing edge of the airfoil and optimizing the shape of the edge did suppress the noise. The experts also found that asymmetrical serrations reduced the noise more than symmetrical serrations.&nbsp;



However, the extent of noise reduction varied with different operating conditions, so the scientists emphasized that the airfoil designs should be further evaluated based on the specific application for which they would be used.



For example, wind turbines have complex incoming flow environments that require a more general noise reduction technology. Examining noise reduction techniques under the influence of different incoming flows would make their conclusions more universal.



The researchers believe their work will serve as an important guide for airfoil design and noise control in the future.



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By <a href="mailto:bosman@truewan.co.za">Alison Bosman</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Owl wings inspire noise reduction in wind turbines and aircraft

The turning blades on wind turbines and drones make a...

Many birds learn their songs in the same way that humans learn a language or dialect –from their parents and neighbors, through mimicry. According to most biologists, this is an uncertain and error-prone method, often resulting in slow but unmistakable changes in the nature of <a href="https://www.earth.com/news/humpback-whale-songs-are-used-to-locate-not-attract-other-whales/">songs</a> over the years.



However, new research led by the <a href="https://www.berkeley.edu/">University of California, Berkeley</a> has found that some isolated populations of double-collared East African sunbirds have been singing the same songs - passed down to each new generation - for up to a million years.&nbsp;



The amazingly static nature of their songs may be due to the birds’ unchanging environment. The birds have inhabited so-called sky islands on East African mountaintops since ancient times.



"If you isolate humans, their dialects quite often change; you can tell after a while where somebody comes from. And song has been interpreted in that same way," said study senior author Rauri Bowie, a professor of Integrative Biology at UC Berkeley. "What our paper shows is that it's not necessarily the case for birds. Even in traits that should be very labile, such as song or plumage, you can have long periods of stasis."



According to Professor Bowie and his colleagues, the idea that birdsong changes very often likely arose from studies of Northern Hemisphere birds, which have repeatedly encountered environmental changes, such as glaciers coming and going over the last thousands of years. These changing environmental conditions can cause significant modifications in plumage, song, and mating strategies.



However, since mountaintop environments in the tropics, particularly in East Africa (such as Mount Kenya or Kilimanjaro) have witnessed very little geological change over the millennia, the birds living there faced no evolutionary pressure to change their plumage or songs.



"We are showing, using a really nice setup where we could look at song evolution using naturally isolated populations, that [in East African sunbirds] you don't see this gradual change through cultural or genetic drift at all," Bowie said. "You see these sharp bursts of change in a trait such a birdsong and lots and lots of evidence for stasis, even when that trait should be very plastic. To me, that was a really fascinating result."



The study is published in the journal <a href="https://royalsocietypublishing.org/doi/10.1098/rspb.2021.2062">Proceedings of the Royal Society B</a>.



---



By <a href="mailto:andrei.ionescu5891@gmail.com">Andrei Ionescu</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

The song of the East African sunbird may be a million years old

Many birds learn their songs in the same way that...

Scientists are transforming chocolate into a functional food by infusing it with probiotics and prebiotics, aiming to create a treat that satisfies cravings while supporting gut health. 



The challenge lies in maintaining chocolate's beloved texture and flavor while adding health benefits.



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https://youtu.be/Ug657J67iEo?si=w96YjGMsg939LD_3
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Probiotics - beneficial microbes that balance gut bacteria and aid digestion - are typically fragile and can be destroyed by stomach acid or processing. 



Prebiotics act as food for these microbes, helping them thrive. Together, they form "synbiotics," a powerful health combination.



Researchers Smriti Gaur and Shubhi Singh from India's Jaypee Institute of Information Technology took an innovative approach, using natural prebiotics like corn and honey instead of complex processing methods. 



They created five chocolate varieties: a control and four synbiotic versions containing different combinations of prebiotics, probiotics (Lactobacillus strains), and flavor enhancers (cinnamon or orange).



Laboratory simulations of human digestion showed the probiotics remained viable for over five hours, suggesting they could survive long enough to benefit gut health.



Taste tests were positive, with researchers particularly enjoying the orange-flavored variety, describing it as having "vibrant citrus notes" complementing the "rich cocoa" with a "luxurious" texture.



This research represents just the beginning. With further refinement of strains, textures, and flavors, chocolate could evolve beyond mere indulgence to become a functional food that nourishes while it delights.



The study is published in the journal <a href="https://pubs.acs.org/doi/10.1021/acsfoodscitech.4c00741" target="_blank" rel="noreferrer noopener">ACS Food Science &amp; Technology</a>.

Is chocolate the next nutritional powerhouse?

Scientists are transforming chocolate into a functional food by infusing...

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Today’s Video of the Day from the <a href="https://www.esa.int/">European Space Agency</a> features Nushagak Bay, a large estuary in southwest Alaska. Nushagak runs mainly north to south and exits in Bristol Bay, a large body of water in the Bering Sea.



"The bay is primarily fed by the Nushagak River, which begins in the Alaska Range and flows southwest approximately 450 km. The bay is also fed by several additional rivers including the Wood, Igushik, Snake and Weary rivers," says ESA.



"The dark colors of the Nushagak River are most likely due to tannins or lignins (chemical substances found in plants). Tannins and lignins from roots, leaves, seeds, bark and soil can leach into the water and give it a brown or even black colour. The sediments then flow southwards where it is mixed with the bluer waters of the bay."



Video/ Image Credit: ESA



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By <a href="http://csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Nushagak Bay in southwest Alaska

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Today's Video of the Day from the <a href="https://www.acs.org/">American Chemical Society</a> (ACS) reveals that proteins on flu viruses are actually flexible, tilting and waving in a “breath-like” motion. According to the experts, these proteins could be used to better defend against the flu.



"The main antigenic targets of influenza virus are two surface glycoproteins, hemagglutinin (HA) and neuraminidase (NA). Whereas the structural and dynamical properties of both glycoproteins have been studied previously, the understanding of their plasticity in the whole-virion context is fragmented," wrote the researchers.



To investigate, the team conducted detailed simulations of the influenza A H1N1 virion, or the swine flu. The experts concluded that the visualizations show many new vulnerable states of flu viruses, which could improve future vaccines and antiviral drugs.



Video/ Image Credit: American Chemical Society&nbsp;



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Editor



Check us out on <a href="https://www.earth.com/earthsnap/">EarthSnap</a>, a free app brought to you by Eric Ralls and Earth.com.

Flu viruses are more flexible than expected

[sendtonews key="G9bUoxcjr4-2511624-12187" type="single"] Today's Video of the Day from the...

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Today’s Video of the Day from the <a href="https://www.esa.int/">European Space Agency</a> features Lake Trasimeno, which is located west of Perugia in central Italy. It is the fourth largest lake in the country. While Trasimeno’s water level varies, it has a maximum depth of approximately six meters.&nbsp;



"In this Copernicus Sentinel-2 image, captured on 6 August 2022, the lake’s emerald green colour is likely due to the presence of phytoplankton. Streaks in the water, particularly visible in the west, indicate the presence of soil and sediments which have been stirred up by winds. Dark colored waters in the southern part of the lake indicate a presence of submerged and floating macrophytes (aquatic plants) as well as algae," says ESA.



"Surrounded by hills on three sides, Trasimeno is subject to heavy storms created by winds, especially from the north and west. There are three islets in the lake: Maggiore, Minore and Polvese (the largest). The lake’s shores are sparsely inhabited with only two popular villages: Castiglione del Lago and Passignano sul Trasimeno."



"Italy is experiencing its worst drought in 70 years which has affected drinking water supplies, hydroelectric power and agricultural production. High temperatures, hot winds and lack of rainfall are the main causes of drought in the Umbrian region which saw Lake Trasimeno’s drop 1.3 m, reaching the limit of the hydrometric zero in July 2022."



Video/Image Credit: ESA&nbsp;



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By <a href="http://csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Lake Trasimeno in Central Italy

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Today's Video of the Day from the <a href="https://www.acs.org/">American Chemical Society</a> describes a new self-powered nanosensor that can instantly detect mercury contamination with the tap of a finger.&nbsp;



The oxidized form of mercury can be harmful when it is ingested through contaminated water or food. This makes it necessary for experts to develop sensors that can quickly and accurately detect the presence of mercury.&nbsp;



Zong-Hong Lin and colleagues have now created a triboelectric nanosensor (TENS) that can detect mercury by simply by touching a sample. According to the researchers, their TENS could serve as the basis for similar devices to safely and remotely monitor other pollutants.



Video Credit: American Chemical Society&nbsp;



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Editor



Check us out on <a href="https://www.earth.com/earthsnap/">EarthSnap</a>, a free app brought to you by Eric Ralls and Earth.com.

Detecting mercury contamination with the tap of a finger

[sendtonews key="LvS8v8bp9z-2564889-12187" type="single"] Today's Video of the Day from the...

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Today’s Video of the Day from the <a href="https://www.acs.org/">American Chemical Society</a> explores the ability of salt to transform the way that foods and beverages taste. Salt is known to cover up undesirable flavors, such as bitterness in coffee or beer, but how exactly does sodium chloride change the taste of other compounds?



One previous study showed that, not only does salt suppress bitterness, but also enhances sweetness and sourness. Another study revealed that bitterness reduction by salt seems to be happening at the tongue receptor level as well as in the brain.&nbsp;



While it is known that salt taste is mediated by the presence of sodium channels in the form of taste buds, experts believe that there is also an unknown receptor responsible for how we taste salt that has not yet been identified.&nbsp;



Video Credit: ACS Reactions



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Editor



Check us out on <a href="https://www.earth.com/earthsnap/">EarthSnap</a>, a free app brought to you by Eric Ralls and Earth.com.

How does salt makes things taste better?

[sendtonews key="X0f6OHYoI4-2310561-12187" type="single"] Today’s Video of the Day from the...

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Today’s Video of the Day from the <a href="https://www.esa.int/">European Space Agency</a> features Santiago, the capital city of Chile. The city is located in the center of the Santiago Metropolitan Region, which has a population of about eight million people.&nbsp;



'The weather of Santiago resembles the Mediterranean climate with dry and warm summers with temperatures reaching up to 35°C (from October to March) and cool and humid winters that can drop to 0°C (from April to September)."



"The city lies in the centre of the country’s central valley around 80 km from the Pacific Ocean to the west and borders Argentina to the east. A tiny part of Argentina is visible in the top-right corner of the image where the mountain crest of the Andes Mountains acts as a divider between the two countries," says ESA.



Video/ Image Credit: ESA



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Editor



Check us out on <a href="https://www.earth.com/earthsnap/">EarthSnap</a>, a free app brought to you by Eric Ralls and Earth.com.

Santiago, Chile in South America

[sendtonews key="JRaP49ISmm-2357509-12187" type="single"] Today’s Video of the Day from the...

Spiral,Galaxy,,Illustration,Of,Milky,Way

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Astronomers at <a href="https://www.jhu.edu/">Johns Hopkins University</a> have created an interactive map of the universe, including the actual position and real colors of 200,000 galaxies. The map allows the public to access data that was previously only available to scientists.



The map was developed using data collected by the Sloan Digital Sky Survey. For over two decades, a telescope in New Mexico was aimed at slightly different locations to capture the night sky.&nbsp;



"Growing up I was very inspired by astronomy pictures, stars, nebulae and galaxies, and now it's our time to create a new type of picture to inspire people," said map creator Brice Ménard, a professor at Johns Hopkins. "Astrophysicists around the world have been analyzing this data for years, leading to thousands of scientific papers and discoveries. But nobody took the time to create a map that is beautiful, scientifically accurate, and accessible to people who are not scientists. Our goal here is to show everybody what the universe really looks like."



"In this map, we are just a speck at the very bottom, just one pixel. And when I say we, I mean our galaxy, the Milky Way which has billions of stars and planets. We are used to seeing astronomical pictures showing one galaxy here, one galaxy there or perhaps a group of galaxies. But what this map shows is a very, very different scale."



"From this speck at the bottom, we are able to map out galaxies across the entire universe, and that says something about the power of science."



The <a href="https://mapoftheuniverse.net/">interactive map</a> is available online, where it can be downloaded for free.



Video Credit: Johns Hopkins&nbsp;



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Editor



Check us out on <a href="https://www.earth.com/earthsnap/">EarthSnap</a>, a free app brought to you by Eric Ralls and Earth.com.

Interactive map of the universe includes 200,000 galaxies

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Lesotho: Africa's "Kingdom in the Sky" Today’s Video of the Day from the <a href="https://www.esa.int/">European Space Agency</a> features northwest Lesotho in South Africa.



According to ESA, Lesotho is the only nation in the world that lies completely above 1,000 m in elevation. The country is famous for its tall mountains and narrow valleys, and is known as Africa's "Kingdom in the Sky."



Out of a population of around two million people, about 80 percent live in rural areas. More than 75 percent of these people are engaged in <a href="https://www.earth.com/news/climate-change-will-have-a-global-impact-on-agriculture/">agriculture</a>, including rainfed cereal production and animal grazing.&nbsp;



ESA reports that the country’s agricultural system faces a growing number of issues, with climate-related vulnerabilities such as drought, floods and extreme temperatures occurring more frequently. 



Diamonds are amongst the minerals found in the mountains. Indeed, Lesotho can truly be called the Kingdom in the Sky. Beautiful, culturally rich, safe, affordable, and easily accessible from Durban and Johannesburg, mountainous Lesotho is a vastly underrated travel destination. the Kingdom of Lesotho (Sotho: 'Muso oa Lesotho) is an enclaved country in southern Africa. It is just over 30,000 km2 (11,583 sq mi) in size and has a population of around 2 million.



Video Credit: ESA&nbsp;&nbsp;



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer 



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Lesotho: Africa's "Kingdom in the Sky"

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Today's Video of the Day from the <a href="https://www.esa.int/">European Space Agency</a> features Dublin, the capital and largest city of Ireland. Beyond its pub culture, Dublin is known as a modern culinary destination and a UNESCO City of Literature.



"Dublin is located near the midpoint of Ireland’s east coast in the province of Leinster. The city, which covers an area of around 115 square kilometers, is bordered by the Dublin Mountains, a low mountain range to the south, and is surrounded by flat farmland to the north and west," says ESA.



"The city straddles the River Liffey, which rises in the Wicklow Mountains and flows around 80 kilometers eastwards through the city of Dublin, in which it is canalised and bordered with quays. It then empties into Dublin Bay, an arm of the Irish Sea."



Dublin has an abundance of green spaces, including one of the largest enclosed public parks in any European capital city. Phoenix Park, which was originally formed as a royal hunting park in the 1660s, includes 707 hectares of green space.



Video Credit: ESA&nbsp;



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Editor



Check us out on <a href="https://www.earth.com/earthsnap/">EarthSnap</a>, a free app brought to you by Eric Ralls and Earth.com.

The city of Dublin on Ireland's east coast

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Today's Video of the Day from the <a href="https://www.esa.int/">European Space Agency</a> features the province of Zaragoza in northeast Spain. The image was captured by the Copernicus Sentinel-2 mission.



"Together with the provinces of Huesca and Teruel, Zaragoza formed the old kingdom of Aragon. Its capital, also called Zaragoza (not visible in this image) is home to around half of Aragon’s population," says ESA.



"The Ebro River can be seen winding its way through the province from west to east in this image. Between its source in the Cantabrian Mountains in the northwest and its delta on the Mediterranean coast, the Ebro River is fed by more than 200 tributaries as it flows 910 km across much of northern Spain."



Since rainfall is very scarce in this region, irrigation in the Ebro basin is critically important. In the valleys surrounding the Ebro River, many fields are used for growing crops such as corn, wheat, and barley.



Video/ Image Credit: ESA



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Editor



Check us out on <a href="https://www.earth.com/earthsnap/">EarthSnap</a>, a free app brought to you by Eric Ralls and Earth.com.

The province of Zaragoza in northeast Spain

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Today’s Video of the Day from <a href="https://earthobservatory.nasa.gov/">NASA Earth Observatory</a> reveals the evolution of the Columbia Glacier in southeastern Alaska. Columbia is among the fastest shrinking glaciers in the world, and the video documents its rapid retreat over the years.&nbsp;



Columbia Glacier is a large, multi-branched calving glacier that flows out of the Chugach Mountains to the Prince William Sound.&nbsp;



According to USGS, Columbia had a long history of stability prior to 1980, with a length 41 miles, and small, short-lived advances or retreats.



In the years since 1980, however, satellite images have captured Columbia’s alarming retreat. By using false-color images, scientists can distinguish between snow and ice, open water, vegetation, and rocky debris on the glacier’s surface.



The series of false-color images featured in today's video were acquired over the span of 35 years. You can see that by 2021, the glacier’s main branch had retreated about 15 miles from its initial position.



The Columbia Glacier has also lost more than 50 percent of its volume, mostly due to calving. <a href="https://www.earth.com/video/nasa-reveals-3d-visual-of-an-atmospheric-river/">NASA</a> reports that while climate change likely started the retreat, mechanical processes kept the disintegration going.



The NASA images are provided by Jesse Allen, Robert Simmon, Joshua Stevens, and Lauren Dauphin using data from Landsat satellites, from the U.S. Geological Survey, and data from MODIS on NASA’s Terra satellite. The structure of Columbia’s moraine played a large role in the stability of the glacier before 1980. 



Like other tidewater glaciers, the Columbia built up a moraine over time, and the mixture of ice and rock functioned like a dam keeping out the sea. It was supported on one end by the shoreline and by the underwater terminal moraine at the other.



Video Credit: NASA Earth Observatory/&nbsp; NASA’s Scientific Visualization Studio



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Editor



Check us out on <a href="https://www.earth.com/earthsnap/">EarthSnap</a>, a free app brought to you by Eric Ralls and Earth.com.

The rapid retreat of the Columbia Glacier

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Today’s Video of the Day from the <a href="https://www.esa.int/">European Space Agency</a> features the Pyrenees Mountains, which form a natural boundary between France and Spain in southwest Europe.



The mountain range is 430 kilometers in length. It stretches from the Mediterranean Sea on the east to the Atlantic Ocean on the west.



At an elevation of 3404 meters, Pico de Aneto is the highest mountain peak in the Pyrenees, and the third-highest peak in Spain. Pico de Aneto is located in the Posets-Maladeta Natural Park, which spans more than 82,000 acres.&nbsp;



"Geological studies have revealed that the Pyrenees Mountains have been around for longer than the Alps, with their sediments first deposited in coastal basins during the Paleozoic and Mesozoic eras," reports ESA.



"The entire mountain range formed due to the upwelling of large sedimentary rocks by the collision of the Iberian and the Eurasian plate around 100 to 150 million years ago, followed by intense erosion from ice and water."



The western Pyrenees receive more precipitation due to moisture blowing in from the Atlantic Ocean. The mountain range contains many lakes, several small glaciers, and some of the highest waterfalls in Europe.



Video &amp; Image Credit: ESA



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Editor



Check us out on <a href="https://www.earth.com/earthsnap/">EarthSnap</a>, a free app brought to you by Eric Ralls and Earth.com.

The Pyrenees Mountains in southwest Europe

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Earth,Like,Exoplanet,3d,Render

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Today's Video of the Day from <a href="https://www.nasa.gov/goddard">NASA Goddard</a> describes two exoplanets that are orbiting a star 218 light-years away. A team of researchers led by the University of Montreal has found evidence that these planets are "water worlds."



The experts used data from NASA’s Hubble and Spitzer Space Telescopes. They discovered that exoplanets Kepler-138 c and Kepler-138 could be composed largely of water.



"We previously thought that planets that were a bit larger than Earth were big balls of metal and rock, like scaled-up versions of Earth, and that's why we called them super-Earths," explained study co-author Björn Benneke.&nbsp;



"However, we have now shown that these two planets, Kepler-138 c and d, are quite different in nature and that a big fraction of their entire volume is likely composed of water. It is the best evidence yet for water worlds, a type of planet that was theorized by astronomers to exist for a long time."



Video Credit: NASA Goddard



Image Credit: NASA, ESA, and Leah Hustak (STScI)



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Editor



Check us out on <a href="https://www.earth.com/earthsnap/">EarthSnap</a>, a free app brought to you by Eric Ralls and Earth.com.

Two distant planets may be "water worlds"

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Satellites reveal how Earth's systems are interconnected Today’s Video of the Day from <a href="https://www.nasa.gov/goddard">NASA Goddard</a> describes Earth’s interconnected systems, and how this network is affected by rising temperatures.&nbsp;



During 2020, average global temperatures matched the hottest year on record. The hurricane season was also record-breaking, with many of the storms intensifying at extraordinary speeds. Hot water in the ocean is fuel for hurricanes. The satellite data shows that it's all one interconnected system showing how Satellites reveal how Earth's systems are interconnected.



According to NASA, dust swept up from Northern Africa plays a major role in the formation of hurricanes, and is also a key source of fertilization in the Amazon rainforest. As a result of<a href="https://www.earth.com/news/seagrass-wasting-disease-is-fueled-by-climate-change/"> climate</a> change, dust plumes are expected to decline, which will have an effect on vegetation far away.&nbsp;



Images from Earth-observing satellites show how the world’s plant life is affected by natural disasters, fires, and deforestation. Satellites also reveal how widespread changes in vegetation impact waterways,&nbsp; the climate, air quality. Satellites communicate by using radio waves to send signals to the antennas on the Earth. "Earth From Space" is a groundbreaking two-hour special that reveals a spectacular new space-based vision of our planet. 



Video Credit: NASA Goddard&nbsp;



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Editor



Check us out on <a href="https://www.earth.com/earthsnap/">EarthSnap</a>, a free app brought to you by Eric Ralls and Earth.com.

Satellites reveal how Earth's systems are interconnected

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Today’s Video of the Day from the <a href="https://welcome.miami.edu/">University of Miami</a> Rosenstiel School of Marine and Atmospheric Science explores how changes in water temperatures have affected tiger shark habitats and movements in the North Atlantic Ocean. The study reveals that rising temperatures have caused the sharks to shift toward the poles over the past 40 years.



“Tiger shark annual migrations have expanded poleward, paralleling rising water temperatures,” explained study lead author Neil Hammerschlag. “These results have consequences for tiger shark conservation, since shifts in their movements outside of marine protected areas may leave them more vulnerable to commercial fishing.”



The researchers analyzed nine years of tracking data from satellite-tagged tiger sharks, combined with four decades of conventional tag and recapture data provided by National Oceanic and Atmospheric Administration (NOAA) Cooperative Shark Tagging Program.



The experts found that during the last decade of record heat, for every one-degree Celsius increase in water temperatures, tiger sharks migrated further poleward by over 400 kilometers. They also migrated two weeks earlier than usual to waters off the northeastern coast of the United States.



“Given their role as apex predators, these changes to tiger shark movements may alter predator-prey interactions, leading to ecological imbalances, and more frequent encounters with humans,” concluded Professor Hammerschlag.



Video Credit: University of Miami Rosenstiel School of Marine and Atmospheric Science



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Editor



Check us out on <a href="https://www.earth.com/earthsnap/">EarthSnap</a>, a free app brought to you by Eric Ralls and Earth.com.

Tiger sharks are shifting poleward as temperatures rise

Today’s Video of the Day from the University of Miami...

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Today’s Video of the Day from the <a href="https://www.esa.int/">European Space Agency</a> is focused on the melt ponds that emerge during the spring and summer on the Greenland Ice Sheet, which is the largest ice mass in the northern hemisphere.



"Melt ponds are vast pools of open water that form on both sea ice and ice sheets and are visible as turquoise-blue pools of water in this Copernicus Sentinel-2 image," says ESA.



"When snow and ice melts atop glaciers, water flows in channels and streams and collects in depressions on the surface. These melt ponds can speed up the melting of the surrounding ice since they greatly reduce the ice’s ability to reflect sunlight."



"This can create a positive feedback where an increasing number of melt ponds absorb more heat which causes ice cover to melt even faster."



According to ESA, Greenland has been hit with a late-season heatwave that began in early September. This caused the type of melt event that usually occurs in the middle of summer.



"In a recent paper published in Nature Climate Change, scientists found that major sea-level rise from the melting of the Greenland ice cap is now ‘inevitable’ even if the burning of fossil fuels were to halt overnight," says ESA. "Using satellite observations of Greenland ice loss and ice cap from 2000 to 2019, the team found the losses will lead to a minimum rise of 27 cm regardless of climate change."



Video Credit: ESA&nbsp;



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Editor



Check us out on <a href="https://www.earth.com/earthsnap/">EarthSnap</a>, a free app brought to you by Eric Ralls and Earth.com.

Melt ponds on the Greenland Ice Sheet

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Today’s Video of the Day from the <a href="https://www.esa.int/">European Space Agency</a> describes a new map of Mars that is providing insight into the planet’s watery past. The map also reveals where future missions could safely land on Mars.&nbsp;



The map has been created over the last decade using observations of water-rich rocks and mineral deposits. The images were captured by ESA’s Mars Express and NASA’s Mars Reconnaissance Orbiter.



"A big surprise is the prevalence of these minerals, with the map revealing hundreds of thousands of water-affected locations in the oldest parts of the planet," says ESA. "The new data will help answer exciting questions about Mars’ climate history, whether water was globally persistent or confined to short, intense episodes, and whether the conditions were ever suitable for life."



"Specifically, the map shows the locations and abundances of aqueous minerals. These are from rocks that have been chemically altered by the action of water in the past, and have typically been transformed into clays and salts."



According to John Carter of the Institut d’Astrophysique Spatiale (IAS), our collective understanding of Mars has been oversimplified. He explained that planetary scientists have tended to think that only a few types of clay minerals on Mars were created during its wet period, then as the water gradually dried up, salts were produced across the planet.



The new map shows that the composition of Mars is much more complicated than what we thought. For example, while many salts formed after Martian clays, there are some salts that are presumed to be older than some of the clays.&nbsp;



“The evolution from lots of water to no water is not as clear cut as we thought, the water didn’t just stop overnight. We see a huge diversity of geological contexts, so that no one process or simple timeline can explain the evolution of the mineralogy of Mars. That’s the first result of our study. The second is that if you exclude life processes on Earth, Mars exhibits a diversity of mineralogy in geological settings just as Earth does,” said Carter.



Video Credit: ESA



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Editor



Check us out on <a href="https://www.earth.com/earthsnap/">EarthSnap</a>, a free app brought to you by Eric Ralls and Earth.com.

The history of Mars is much more complex than we thought

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Today's Video of the Day from the <a href="https://www.stowers.org/">Stowers Institute for Medical Research</a> describes how cavefish adapted to a sedentary lifestyle over tens of thousands of years. 



The experts found that the muscle metabolism of cavefish has been genetically reprogrammed over time. As a result, the animals have experienced major changes in their morphology and behavior. Despite these changes, however, the cavefish remain healthy and fit.



The research may provide new clues about the evolutionary consequences of prolonged physical inactivity in humans.&nbsp;



“It’s no surprise that people are moving less and less as technology has advanced,” said Rohner. “With cavefish, we have a unique system where we can study what might happen if people remained couch potatoes over very, very long periods of time.”



Video Credit: Stowers Institute for Medical Research



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Editor



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Cavefish are healthy despite their sedentary lifestyle

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Today’s Video of the Day from <a href="https://earthobservatory.nasa.gov/">NASA Earth Observatory</a> some of the most incredible waves in the world, as seen by Landsat satellites.



"With more than 370,000 miles of coastline on Earth, there are plenty of places where epic waves build up, curl over, and hurtle toward the shore.- much to the thrill of surfers," says NASA. "There are some places where these waves are so magnificent that they can be seen from space."



"With the broad perspective of satellites, we can see how these iconic waves develop into the world’s tallest, longest, fastest, and heaviest."



Video Credit: NASA Earth Observatory&nbsp;



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By <a href="mailto:csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Editor



Check us out on <a href="https://www.earth.com/earthsnap/">EarthSnap</a>, a free app brought to you by Eric Ralls and Earth.com.

Satellites capture the world's biggest and fastest waves

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