A new study from <a href="https://www.osu.edu/">Ohio State University</a> reveals what is going on inside of your <a href="https://www.earth.com/news/gut-brain-interactions-have-an-influence-on-diseases/">brain</a> when you get lost in a fictional fantasy. The experts discovered that the more immersed we become in the lives of our favorite characters of fiction, the more our brain activity reflects how much we identify with them.
&#8220;When they think about a favorite fictional character, it appears similar in one part of the brain as when they are thinking about themselves,&#8221; said study lead author Timothy Broom.
The research was focused on self-described fans of the HBO series &#8220;Game of Thrones.&#8221; The individuals were instructed to think about themselves, nine of their friends, and nine characters from the drama series. The participants also reported on which character they felt closest to and liked the most.
According to Broom, Game of Thrones was ideal for this study because it attracted a devoted fan base and the large cast presented a variety of characters that people could become attached to.
One of the key findings involved participants who scored highest on &#8220;trait identification.&#8221; These individuals agreed most strongly with statements like &#8220;I really get involved in the feelings of the characters in a novel.&#8221;
&#8220;People who are high in trait identification not only get absorbed into a story, they also are really absorbed into a particular character,&#8221; said Broom. &#8220;They report matching the thoughts of the character, they are thinking what the character is thinking, they are feeling what the character is feeling. They are inhabiting the role of that character.&#8221;
The researchers used an fMRI machine to measure activity in various parts of the brain through small changes in blood flow. As the participants&#8217; brains were scanned, they were evaluating themselves, their friends, and Game of Thrones characters. 
A part of the brain called the ventral medial prefrontal cortex (vMPFC) is known to show increased activity when people think about themselves and, to a lesser extent, when they think about close friends.
While in the fMRI, the individuals were shown a series of names &#8211; including themselves, friends, or characters &#8211; along with a trait, such as lonely, sad, trustworthy, or smart. The participants simply said &#8220;yes&#8221; or &#8220;no&#8221; to imply whether the trait fit the person.
As expected, the vMPFC was most active when people were evaluating themselves, less active when they evaluated friends, and least active when they evaluated characters from Game of Thrones.
However, among those who were high in trait identification, the vMPFC was more active when they thought about the fictional characters than it was for participants who identified less with the characters. This region of the brain was particularly active when the individuals evaluated the character they identified with the most.
Study co-author Dylan Wanger said the findings help explain how fiction can have such a big impact on some people.
&#8220;For some people, fiction is a chance to take on new identities, to see worlds though others&#8217; eyes and return from those experiences changed,&#8221; said Wagner.
&#8220;What previous studies have found is that when people experience stories as if they were one of the characters, a connection is made with that character, and the character becomes intwined with the self. In our study, we see evidence of that in their brains.&#8221;
The study is published in the journal <a href="https://academic.oup.com/scan">Social Cognitive and Affective Neuroscience</a>.
&#8211;&#8212;
By <a href="http://csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

What happens in your brain while you're lost in fiction

Why is a good night’s sleep so crucial for a sharp memory? A team of neuroscientists has taken a major step toward answering this question.&nbsp;



By monitoring brain activity in rats for up to 20 hours after a learning task, they discovered that sleep reorganizes neural patterns in a way that helps memories take hold and prepares the brain for new information.&nbsp;



The study, led by researchers from the <a href="https://ista.ac.at/en/home/" target="_blank" rel="noreferrer noopener">Institute of Science and Technology Austria</a> (ISTA), offers new insights into how the brain engraves long-term memories during times of rest.



<h2 class="wp-block-heading" id="h-monitoring-brain-cell-activity-during-sleep">Monitoring brain cell activity during sleep</h2>



<a href="https://www.earth.com/news/sleep-is-essential-for-memory-formation/" target="_blank" rel="noreferrer noopener">Sleep</a>’s role in helping animals remember things - like where food is hidden - has long been known. But scientists still don’t fully understand how this happens at the neuronal level.&nbsp;



To investigate, the ISTA team focused on <a href="https://www.earth.com/news/chimpanzees-have-remarkable-spatial-memory-and-sense-of-direction/" target="_blank" rel="noreferrer noopener">spatial memory</a>, by training rats to locate food rewards in a maze while recording brain activity using a wireless system.&nbsp;



The setup allowed them to monitor hippocampal neurons, which play a key role in spatial navigation and learning, for up to 20 continuous hours of sleep following the task.



“We showed that the neuronal assemblies in the early stages of sleep reflect recently learned spatial memories. However, as sleep progresses, neuronal activity patterns gradually transform into those seen later, when the rats awaken and remember the locations of their food rewards,” explained Professor Jozsef Csicsvari, the senior author of the study.



<h2 class="wp-block-heading" id="h-the-hippocampus-as-a-map-maker">The hippocampus as a map maker</h2>



Earlier research has shown that the hippocampus creates internal “maps” of an animal’s environment by firing specific neurons at specific locations. These mental maps are updated during learning and become especially focused around important activities, like where food is found.&nbsp;



The hippocampus continues to play a vital role during sleep by replaying memory traces, a process called reactivation.



Previous work by the Csicsvari group showed that the more frequently the hippocampus reactivated a reward location during sleep, the better the animal remembered it later. When this replay was blocked, the rats struggled to recall the location - suggesting that reactivation is key to cementing memory.



<h2 class="wp-block-heading" id="h-memory-patterns-shift-during-sleep">Memory patterns shift during sleep</h2>



Until now, such studies were limited to short sleep sessions lasting just a few hours. In the new study, the team extended the recordings to cover a full overnight sleep.&nbsp;



The extended monitoring revealed a previously unseen phenomenon: memory-related neural patterns shifted gradually during sleep.



“Our findings were unexpected,” said co-first author Lars Bollmann. “We showed that the activity patterns of neurons linked to the reward locations reorganized during the long sleep.”



Initially, when the rats entered sleep, the same neurons that were active during learning remained active, forming what the researchers called a “stable subgroup.”&nbsp;



But as sleep progressed, some of these neurons stopped firing and new neurons took their place. By the end of the sleep period, the firing pattern had evolved to resemble the one seen when the rats successfully remembered the reward locations the next day.



This representational shift occurred specifically during non-REM sleep, the researchers found, while REM sleep seemed to prevent or counteract this reorganization.



<h2 class="wp-block-heading" id="h-making-room-for-new-memories">Making room for new memories</h2>



What’s the point of this neural reshuffling? The researchers suggest it could be a way for the brain to optimize its memory storage.



“It is possible that memory representations must be formed quickly during <a href="https://www.earth.com/news/secrets-of-learning-how-the-brain-stores-new-information/" target="_blank" rel="noreferrer noopener">learning</a> but that such representations are not optimal for long-term storage,” Csicsvari explained.&nbsp;



“Therefore, a process may take place in sleep that optimizes these representations to reduce brain resources to store a specific memory.”



In other words, by trimming down the number of neurons needed to represent a particular memory, the brain may free up resources for encoding new experiences.&nbsp;



Supporting this idea, the researchers found that fewer neurons were linked to a given reward location after sleep than before.



“Any new memories must find a way to be integrated into existing knowledge,” Csicsvari adds. “Frequent repetitions of the new memories as well as partial change in the neuronal code may thus help optimize their integration into existing memory representations.”



<h2 class="wp-block-heading" id="h-understanding-sleep-and-memory">Understanding sleep and memory</h2>



This study marks a significant advance in understanding how sleep strengthens memory. By showing that the brain reorganizes memory representations over the course of sleep - and by linking these shifts to improved recollection - the research sheds light on one of the most essential functions of sleep.



While the findings come from animal models, they offer promising avenues for future research into human memory and the consequences of <a href="https://www.earth.com/news/study-reveals-sex-differences-in-sleep-disorders/" target="_blank" rel="noreferrer noopener">sleep disorders</a>.&nbsp;



As scientists continue to explore how memories evolve overnight, they may eventually uncover strategies for enhancing learning, supporting brain health, and even treating memory-related conditions.



The study is published in the journal <a href="http://dx.doi.org/10.1016/j.neuron.2025.02.025" target="_blank" rel="noreferrer noopener">Neuron</a>.



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Sleep rewires the brain to strengthen memories

Why is a good night’s sleep so crucial for a...

A new long-term study indicates that children who spend more time on screens during their early years - particularly on phones and tablets - experience higher levels of stress and depressive symptoms once they enter adolescence.&nbsp;



The eight-year study, conducted in Finland and published in the journal <a href="https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2830233" target="_blank" rel="noreferrer noopener">JAMA Network Open</a>, offers fresh insights for parents deciding when and how to give their kids digital access, especially given rising <a href="https://www.earth.com/news/mental-health-crisis-half-of-the-worlds-population-will-be-affected-by-age-75/" target="_blank" rel="noreferrer noopener">mental health</a> challenges among younger populations.



According to the experts, between one-quarter and one-third of adolescents worldwide experience mental health issues, with first symptoms usually appearing during the teenage years.&nbsp;



The researchers see their findings as additional evidence that parents might want to limit screen time and encourage active play, since cultivating certain habits early may serve as a buffer against future psychological distress.



<h2 class="wp-block-heading" id="h-screens-and-teen-health">Screens and teen health</h2>



Scientists drew data from the <a href="https://www.panicstudy.fi/" target="_blank" rel="noreferrer noopener">Physical Activity and Nutrition in Children</a> (PANIC) study, a project tracking 187 Finnish kids from ages 6–9 to around 15–16. Over the course of eight years, the team monitored the participants’ <a href="https://www.earth.com/news/fitness-focused-medicine-physical-activity-reduces-chronic-disease-risk/" target="_blank" rel="noreferrer noopener">physical activity</a>, <a href="https://www.earth.com/news/too-much-screen-time-is-making-teens-anxious/" target="_blank" rel="noreferrer noopener">screen time</a>, sleep patterns, and eating behaviors.&nbsp;



Then, as teenagers, those same participants were assessed for mental health using standardized measures of stress and depressive symptoms.



The findings revealed that teens who accumulated more total screen time, specifically on mobile devices, ended up showing significantly higher levels of stress and depression.&nbsp;



In fact, the connection between mobile device use and depression was described as a moderate effect size that the scientists find substantial.



<h2 class="wp-block-heading" id="h-the-role-of-physical-activity">The role of physical activity</h2>



Encouragingly, a high level of physical activity during childhood proved to have the opposite effect. 



Teens who remained active - particularly in structured or supervised settings - demonstrated stronger mental health outcomes, even after accounting for factors like body composition, puberty stage, and parents’ educational background. 



This trend was more pronounced among boys, who seemed to receive a larger protective effect against stress from exercise than girls.



Meanwhile, diet quality and sleep duration did not show notable links to teen mental health in this research.&nbsp;



While that does not rule out their importance for overall well-being, it suggests that daily movement and minimized screen time may have more pronounced effects when it comes to adolescent stress and depression.



<h2 class="wp-block-heading" id="h-early-interventions-for-screen-habits">Early interventions for screen habits</h2>



For those wary of introducing personal devices too early, the study’s conclusion is clear: childhood screen behavior can echo into the teenage years, shaping emotional health. Researchers especially emphasize caution with mobile device use.&nbsp;



Balanced approaches appear to matter most. Kids who paired more screen time with lower physical activity ended up with the worst mental health outcomes.&nbsp;



This highlights that focusing on just one of these factors - reducing screen time or encouraging regular exercise - may be less effective than addressing both.



The authors also point out that supervised physical activities, such as team sports, can have particularly strong benefits. This could fuel arguments for policies that increase children’s access to organized athletics, either through schools or community programs.&nbsp;



The study further indicates that mental health professionals should consider routine inquiries about technology habits as part of early interventions.



<h2 class="wp-block-heading" id="h-a-shifting-technological-landscape">A shifting technological landscape</h2>



While the study results are not strictly causal, they highlight the power of everyday choices in shaping long-term psychological outcomes. Given how quickly technology evolves, the authors warn that this knowledge becomes more urgent.&nbsp;



Social media platforms and mobile games continue to expand, and children are exposed to smartphones at younger ages, making it crucial to recognize how these patterns might affect their mental well-being.



Notably, the study concluded before the explosion in newer social media apps, so the current generation may be seeing even more digital consumption.&nbsp;



That said, the fundamental takeaway - that more screens plus less physical activity predicts a rougher mental health path - likely remains valid.



<h2 class="wp-block-heading" id="h-research-limitations-and-future-directions">Research limitations and future directions</h2>



While the study’s eight-year timeframe offers valuable longitudinal data, the final sample of 187 adolescents is small. Many participants dropped out midway, so the final group may not be entirely representative.&nbsp;



Also, while the researchers tracked overall screen time, they did not distinguish between different types of screen exposure or social media content. Future studies might look at which specific apps or games pose the highest risks.



The research also measured sleep duration but not <a href="https://www.earth.com/news/sleep-quality-is-determined-by-daily-activities/" target="_blank" rel="noreferrer noopener">sleep quality</a>, leaving open questions about how nighttime device use might undermine rest and, in turn, mental health.&nbsp;



Most notably, the authors highlight that the data cannot prove that one factor directly causes the other. It’s possible, for instance, that children already prone to stress or depression might gravitate more toward screens.



Still, as mental health difficulties among younger demographics continue to rise, these findings can guide parents and care providers.



Ensuring kids stay active may mitigate some of those effects, but the broader message is that habits formed early can shape teens’ emotional landscapes in the years to come.



In essence, the authors advise parents to craft balanced digital environments, offering moderate device access and ample opportunities for physical activity and <a href="https://www.earth.com/news/social-activity-may-delay-the-onset-of-dementia-by-years/" target="_blank" rel="noreferrer noopener">social engagement</a>.&nbsp;



By doing so, families can help build a foundation of healthier emotional states that carry forward into the challenging teen years.



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Children’s screen time shapes their mental health as teens

A new long-term study indicates that children who spend more...

Sharks have roamed the oceans for millions of years. Their powerful jaws and sharp teeth make them top predators that are capable of influencing entire marine ecosystems. 



However, understanding what they eat and where they feed remains difficult. This is especially true for rare or protected species where direct sampling poses legal and ethical challenges.



Traditionally, scientists study shark diets by examining their teeth. But collecting samples from live sharks can be risky, costly, and often impossible, especially when dealing with <a href="https://www.earth.com/news/why-some-great-hammerhead-sharks-rarely-leave-home/" target="_blank" rel="noreferrer noopener">threatened species</a>. 



Yet, every opportunity to gather data matters. That’s where the past meets the present - inside the drawers and display cases of museums.



A new study led by researchers from Flinders University has found that preserved shark jaws - often considered to be static relics - can be a powerful scientific resource. 



Using teeth from sharks in historical collections, researchers can now study shark diets without touching a living specimen.



This breakthrough offers new hope for <a href="https://www.earth.com/news/one-third-of-shark-species-face-extinction-despite-fishing-bans/" target="_blank" rel="noreferrer noopener">marine science</a> and conservation.



<h2 class="wp-block-heading" id="h-shark-jaws-reveal-feeding-secrets">Shark jaws reveal feeding secrets</h2>



Shark teeth hold chemical signatures that reveal details of their past meals and feeding grounds. These signatures come from ratios of stable isotopes - naturally occurring variations of chemical elements. By examining these isotopes, scientists can piece together an animal’s ecological history.



Until now, scientists avoided using preserved jaws due to concerns that cleaning chemicals might have distorted the isotopes.



Many <a href="https://www.earth.com/news/mediterranean-sharks-face-growing-threats-despite-conservation-efforts/" target="_blank" rel="noreferrer noopener">shark</a> jaws in museums and private collections have been treated with substances like ethanol, bleach, or hydrogen peroxide. These treatments whiten the teeth but were thought to possibly alter their chemical composition.



However, the new research shows otherwise. The team discovered that these chemicals do not affect the key isotopes used in diet studies. This means that thousands of jaws from past decades are now usable in ways previously thought impossible.



"Most shark jaws in museums and private collections are chemically treated, so understanding if, or how these treatments affect tooth isotopes is crucial," said Flinders research associate Dr. Lauren Meyer.



"Finding that preservation chemicals had no impact on isotope values opens the door for the use of jaws from historic collections across Australia and globally."



This discovery means scientists can study <a href="https://www.earth.com/news/sharks-may-benefit-from-rising-temperatures-but-not-from-rising-co2/" target="_blank" rel="noreferrer noopener">shark</a> diets without needing fresh tissue samples. It also significantly broadens the scope of possible studies, including comparative diet research across different eras and regions.



<h2 class="wp-block-heading" id="h-chemical-clarity-through-isotope-testing">Chemical clarity through isotope testing</h2>



The study involved stable isotope analysis, which looks at carbon, nitrogen, and sulfur isotopes. These elements help identify where and what an <a href="https://www.earth.com/news/megalodon-was-sleeker-and-longer-than-previously-imagined/" target="_blank" rel="noreferrer noopener">animal</a> has been eating.



"The chemicals in teeth provide a story of what the shark has eaten and from where, whether that be sea lions in South Australia, or tuna in New South Wales," explained lead author Laura Holmes, from the Southern Shark Ecology Group in the College of Science and Engineering at <a href="https://www.flinders.edu.au" target="_blank" rel="noreferrer noopener">Flinders University</a>.



The researchers partnered with the Isotope Ratio Mass Spectrometry Laboratory at the <a href="https://www.utas.edu.au" target="_blank" rel="noreferrer noopener">University of Tasmania</a>. 



The team tested teeth from three very different elasmobranchs: cownose rays, gummy sharks, and broadnose sevengill sharks.



Despite their structural differences, all samples held up under isotope testing.



<h2 class="wp-block-heading" id="h-rare-species-now-within-scientific-reach">Rare species now within scientific reach</h2>



Access to historical jaws brings particular value when studying rare or threatened shark species. These species often cannot be sampled directly, but many have had jaws collected as trophies. 



With these now validated as reliable data sources, older specimens can help researchers understand long-term dietary trends.



"This is especially useful for rare or threatened species, for which standard tissue samples may not be readily available, but for which trophy jaws have been collected, such as white sharks, tiger sharks, and makos," said Dr. Meyer.



Older collections, such as those from the 1970s and 1980s, now offer a scientific window into the past. This information is crucial as many shark species face increasing pressure from human activities, climate change, and habitat degradation.



<h2 class="wp-block-heading" id="h-applications-across-marine-life">Applications across marine life</h2>



While this study focused on sharks and rays, the implications go beyond these groups.



Other marine predators, such as killer whales, sperm whales, and fur seals, also have teeth stored in museum collections. These could be tested using the same methods, opening new research pathways.



"This study opens the door to use a tremendous resource of samples to untangle the current and historic diet and foraging habitats of complex predators - making the most exciting finding from this study the capacity for new research that is now possible," said Dr. Meyer.



These findings not only expand the toolkit for marine scientists but also enhance our understanding of ocean ecosystems over time. Every preserved tooth could tell a story. 



The study is published in the journal <a href="https://www.sciencedirect.com/science/article/pii/S0141113625001205?via%3Dihub" target="_blank" rel="noreferrer noopener">Marine Environmental Research</a>.



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Chemical clues from old shark jaws reveal diets and habitats

Sharks have roamed the oceans for millions of years. Their...

In the forests of Tanzania, chimpanzees have long been known to fish for termites using handmade tools crafted from local plants. But what makes this behavior even more fascinating is how carefully they seem to choose the materials for their tools.



New research now shows that these <a href="https://www.earth.com/news/primates-face-an-uncertain-future-due-to-climate-change/" target="_blank" rel="noreferrer noopener">primates</a> are not just grabbing any nearby stick to poke into a termite nest - they’re making smart choices based on how flexible and effective the material is.



This discovery comes from a collaborative effort between researchers at the University of Oxford’s <a href="https://www.anthro.ox.ac.uk/" target="_blank" rel="noreferrer noopener">School of Anthropology</a> and Museum Ethnography, the Max Planck Institute for Evolutionary Anthropology, the Jane Goodall Institute in Tanzania, the University of Algarve, the University of Porto in Portugal, and the University of Leipzig.



The study sheds light on the technical thinking behind chimpanzee tool use, a largely invisible part of primate evolutionary history.



<h2 class="wp-block-heading" id="h-chimpanzees-prefer-flexible-tools-for-fishing">Chimpanzees prefer flexible tools for fishing</h2>



To eat <a href="https://www.earth.com/news/termites-are-natures-architects-building-well-ventilated-nests/" target="_blank" rel="noreferrer noopener">termites</a>, chimpanzees must first catch them. The primates use thin plant probes to pull the insects carefully out of narrow, winding tunnels inside termite mounds.



The team proposed that flexible tools would work better in these tight spaces than rigid sticks. To test this, lead author Alejandra Pascual-Garrido brought a portable mechanical tester to Gombe Stream National Park. She measured the amount of force it took to bend different plant materials.



The results were striking. <a href="https://www.earth.com/news/plants-can-sense-when-something-touches-them-despite-not-having-nerves/" target="_blank" rel="noreferrer noopener">Plants</a> that the chimpanzees actually used were much more flexible than those that were available but ignored. 



On average, unused plants were 175 percent more rigid. Even among plants growing side-by-side near the termite mounds, the ones that were repeatedly used produced significantly more flexible tools.



“This is the first comprehensive evidence that wild chimpanzees select tool materials for <a href="https://www.earth.com/news/chimpanzees-have-a-peak-season-for-termite-fishing/" target="_blank" rel="noreferrer noopener">termite fishing</a> based on specific mechanical properties,” said Pascual-Garrido, who has been studying chimpanzee tool-making in Gombe for over ten years.



<h2 class="wp-block-heading" id="h-shared-preferences-across-africa">Shared preferences across Africa</h2>



Interestingly, the same plant species used by chimpanzees in Gombe such as Grewia - are also used by other chimpanzee populations living thousands of kilometers away.



This pattern suggests that the mechanical qualities of these plants are so useful that they’ve become common knowledge among different chimpanzee groups. It also hints that this knowledge might be deeply embedded in <a href="https://www.earth.com/news/chimpanzee-cultures-are-more-complex-than-we-realized/" target="_blank" rel="noreferrer noopener">chimpanzee culture</a>.



Their choices suggest a kind of natural logic. Chimpanzees may have what scientists call a “folk physics” - an intuitive understanding of which materials will get the job done.



Their knack for selecting the right plant isn’t just done by trial and error. It’s a skill. And it's one that might reflect the kind of thinking our early human ancestors used when building their own tools.



“This novel approach, which combines biomechanics with animal behaviour, helps us better understand the cognitive processes behind chimpanzee tool construction and how they evaluate and select materials based on functional properties,” said Pascual-Garrido.



<h2 class="wp-block-heading" id="h-new-questions-about-chimpanzees">New questions about chimpanzees </h2>



The research opens up more questions than it answers. How do young chimpanzees learn which materials to use? Do they copy their mothers? And do they apply the same rules when choosing tools for other jobs - like collecting ants or honey?



“This finding has important implications for understanding how humans might have evolved their remarkable tool using abilities,” explained Adam van Casteren from the Department of Human Origins at the Max Planck Institute for Evolutionary Anthropology.



“While perishable materials like wood rarely survive in the archaeological record, the mechanical principles behind effective tool construction and use remain constant across species and time.”



These behaviors also raise questions about memory, experience, and even innovation in non-human primates. 



<h2 class="wp-block-heading" id="h-clues-about-early-humans">Clues about early humans</h2>



Understanding how chimpanzees refine their techniques over time could reveal a primitive form of trial-and-error learning that mirrors early human problem-solving.



By studying chimpanzees and their preferences for certain types of materials, researchers hope to uncover clues about how early humans may have started crafting implements long before stone tools appeared in the archaeological record.



It’s a small but meaningful step toward understanding the roots of human intelligence - through the eyes, and hands, of our closest extant relatives.



The full study was published in the journal <a href="https://www.cell.com/iscience/fulltext/S2589-0042(25)00419-5?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS2589004225004195%3Fshowall%3Dtrue" target="_blank" rel="noreferrer noopener">iScience</a>.



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Chimpanzees select the best materials for termite fishing

In the forests of Tanzania, chimpanzees have long been known...

In the heart of the Lighthouse Reef Atoll, off the coast of Belize in the Caribbean, lies a fascinating geological wonder - the Great Blue Hole. This vast, circular sinkhole bears an uncanny resemblance to a giant oceanic eye gazing up at the sky.



Nestled in the turquoise waters of the atoll, about 43 miles from the coast of Belize, this dark circular pit is surrounded by coral and contains sediments that tell a story about centuries of storms.



The Great Blue Hole began as a limestone cave on a dry island. During the last ice age, its roof collapsed, leaving it open to the elements. Today, this underwater cave plunges to a depth of 410 feet, spans 980 feet, and is one of the most fascinating places to scuba dive.



As glaciers melted and sea levels rose, the cave filled with water, turning it into a natural vault of sediment that has quietly recorded the passage of time.



In the summer of 2022, a team of scientists from <a href="https://www.goethe-university-frankfurt.de/en" target="_blank" rel="noreferrer noopener">Goethe University Frankfurt</a> led a mission to explore this hidden archive. Funded by the German Research Foundation, the researchers brought a drilling platform out to sea and extracted a 30-meter-long sediment core from the bottom of the Great Blue Hole.



The analysis, carried out by researchers from the universities of Frankfurt, Cologne, Göttingen, Hamburg, and Bern, has given new insight into storm history and climate change in the southwestern Caribbean.



<h2 class="wp-block-heading" id="h-storm-record-written-in-sediment">Storm record written in sediment</h2>



Roughly 7,200 years ago, the limestone island that once held the Great Blue Hole was overtaken by the sea. Since then, layers of sediment have quietly accumulated at the bottom of the underwater cave.



These layers act like a natural time capsule, offering a window into 5,700 years of storm activity. Each layer records the passing of time, just as is found in <a href="https://www.earth.com/news/californias-weather-extremes-found-in-600-year-old-tree-rings/" target="_blank" rel="noreferrer noopener">tree rings</a>.



“Due to the unique environmental conditions – including oxygen-free bottom water and several stratified water layers – fine marine sediments could settle largely undisturbed in the Great Blue Hole,” said Dr. Dominik Schmitt, a researcher in the Biosedimentology Research Group at Goethe University Frankfurt.



“Inside the sediment core, they look a bit like tree rings, with the annual layers alternating in color between gray-green and light green depending on organic content.”



But not all layers are the same. Some are made up of coarser, lighter-colored particles. 



These event layers, called tempestites, formed when powerful waves from hurricanes and tropical storms swept coarse material from the atoll’s outer reef into the hole. 



“The tempestites stand out from the fair-weather gray-green sediments in terms of grain size, composition, and color, which ranges from beige to white,” Schmitt added.



<h2 class="wp-block-heading" id="h-long-term-climate-patterns">Long-term climate patterns </h2>



The team identified and dated 574 individual storm events that were preserved in the sediment core. This detailed storm record stretches far beyond the reach of written or instrumental history, which only covers about 175 years. 



The results offer a unique look into long-term climate patterns and <a href="https://www.earth.com/news/scientists-propose-adding-a-category-6-to-the-current-hurricane-intensity-scale/" target="_blank" rel="noreferrer noopener">hurricane</a> behavior in the region.



The data paints a clear picture: storm activity in the southwestern Caribbean has steadily risen over the past 6,000 years.



“A key factor has been the southward shift of the equatorial low-pressure zone. Known as the <a href="https://www.earth.com/news/tropical-rains-will-shift-northward-in-the-coming-decades/" target="_blank" rel="noreferrer noopener">Intertropical Convergence Zone</a>, this zone influences the location of major storm formation areas in the Atlantic and determines how tropical storms and hurricanes move and where they make landfall in the Caribbean,” Schmitt said.



The researchers also discovered a connection between sea surface temperatures and storm frequency. Warmer waters matched up with periods of increased storm activity. 



“These shorter-term fluctuations align with five distinct warm and cold climate periods, which also impacted water temperatures in the tropical Atlantic,” Schmitt noted.



<h2 class="wp-block-heading" id="h-a-warning-from-the-storm-record">A warning from the storm record</h2>



Historical averages suggest that the Great Blue Hole experienced between four and sixteen major storms per century. However, the sediment record shows that nine storms have already occurred in just the past 20 years.



“Our results suggest that some 45 tropical <a href="https://www.earth.com/news/record-heat-fueled-unexpected-and-deadly-storms-in-2023/" target="_blank" rel="noreferrer noopener">storms</a> and hurricanes could pass over this region in our century alone. This would far exceed the natural variability of the past millennia,” said Prof. Eberhard Gischler of Goethe University Frankfurt.



The team emphasizes that natural climate changes alone cannot explain this dramatic increase. Instead, they point to human-driven global warming. 



The rise in ocean temperatures and the growing strength of La Niña events are creating the perfect conditions for more frequent and more intense storms.



<h2 class="wp-block-heading" id="h-a-sediment-core-with-a-message">A sediment core with a message</h2>



The Great Blue Hole, once thought to be a quiet underwater marvel, is now telling a louder story - one of climate shifts and increasing storm risk.



As the sediment layers continue to build, so does the urgency to address the accelerating pace of extreme weather. 



This research reminds us that history, especially the kind written in mud and sand, still has much to teach us.



The full study was published in the journal <a href="https://www.science.org/doi/10.1126/sciadv.ads5624" target="_blank" rel="noreferrer noopener">Science Advances</a>.



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Sediment in the Great Blue Hole reveals an alarming storm record

In the heart of the Lighthouse Reef Atoll, off the...

The feeling of fullness after a nice meal usually prevents us from eating more. This is a familiar experience for humans, but we are not alone. We share this with starfish and many other organisms as well.



New research indicates that the same message instructing us to eat no more has existed for more than 500 million years. The same molecule affecting our feeding behavior in this way also acts on starfish and other sea animals.



Researchers at <a href="https://www.qmul.ac.uk/" target="_blank" rel="noreferrer noopener">Queen Mary University of London</a> have followed the evolutionary trail of a neurohormone named bombesin, which regulates appetite in humans. 



Collaborating with colleagues at the Institut Pasteur in Paris and the University of Warwick, the researchers discovered that this satiety-inducing peptide is much older than was thought, and is found in animals that lived before the first <a href="https://www.earth.com/news/over-half-of-the-worlds-vertebrates-reside-in-the-tropics/" target="_blank" rel="noreferrer noopener">vertebrates</a> set foot on Earth.



<h2 class="wp-block-heading" id="h-what-is-bombesin">What is bombesin?</h2>



Bombesin is a small peptide that helps regulate appetite by sending a message when it's <a href="https://www.earth.com/news/neurons-discovered-that-tell-us-when-to-stop-eating/" target="_blank" rel="noreferrer noopener">time to stop eating</a>. While it’s been studied in humans and other mammals, its origins were less understood - until now. 



Researchers discovered that a bombesin-like molecule is present in echinoderms like starfish, sea urchins, and sea cucumbers.



If you’re wondering about the unusual name, bombesin isn’t explosive. It’s named after the fire-bellied toad, Bombina bombina, where it was first identified in 1971. 



Scientists noticed that injecting this compound into <a href="https://www.earth.com/news/evolutionary-mystery-why-are-mammals-the-only-vertebrates-to-have-only-one-lower-jawbone/" target="_blank" rel="noreferrer noopener">mammals</a> caused them to eat less and take longer between meals. This led to the idea that bombesin-like neurohormones are part of the body’s natural appetite control system.



Today, compounds that mimic bombesin are being explored as potential treatments for obesity, alongside well-known medications like Ozempic.



<h2 class="wp-block-heading" id="h-a-needle-in-a-haystack">A needle in a haystack</h2>



The research team began by searching for bombesin-like genes in <a href="https://www.earth.com/news/ocean-noise-can-be-fatal-to-marine-invertebrates/" target="_blank" rel="noreferrer noopener">marine invertebrates</a>. 



“It was a bit like looking for a needle in a haystack,” said Professor Maurice Elphick. “But eventually we discovered genes encoding a bombesin-like neurohormone in the genomes of starfish and their relatives.”



Once the gene was identified in the common starfish (Asterias rubens), scientists named the molecule ArBN. 



Collaborators at the University of Warwick used mass spectrometry to determine the exact structure of ArBN, which allowed the molecule to be synthesized for lab testing.



<h2 class="wp-block-heading" id="h-watching-starfish-eat-or-not-eat">Watching starfish eat - or not eat</h2>



<a href="https://www.earth.com/news/starfish-break-off-their-arms-to-evade-danger-and-regenerate-them-later/" target="_blank" rel="noreferrer noopener">Starfish</a> feed in a bizarre and fascinating way: they push their stomachs out through their mouths to digest prey like mussels. The team wanted to know how ArBN affected this feeding behavior.



“When I tested ArBN, I saw that it caused contraction of the starfish stomach. This suggested that ArBN might be involved in stimulating stomach retraction when starfish stop feeding. And this is exactly what I found," explained Dr. Weiling Huang, who conducted the behavioral tests. 



"When I injected ArBN into starfish with their stomachs everted, it triggered the stomach to retract back into the mouth. What’s more, ArBN also delayed the initiation of feeding, as starfish injected with ArBN took longer to enclose a mussel compared to those injected with water.”



<h2 class="wp-block-heading" id="h-a-molecule-older-than-starfish">A molecule older than starfish</h2>



Understanding that bombesin-like molecules have been regulating feeding behavior since before the rise of vertebrates adds an important piece to the puzzle of how appetite evolved. 



“We can infer that this function extends back half-a-billion years to the common ancestor of starfish, humans, and other vertebrates,” said Professor Elphick.



But the implications go beyond biology textbooks. Some species of starfish are moving into new habitats due to climate change. In particular, these species are seeking cooler waters where shellfish farms are located, and may threaten aquaculture operations.



“One of the consequences of climate change is that some starfish species are invading cooler waters where shellfish are cultivated for human consumption,” said Professor Elphick.



“Discovering molecules that inhibit feeding in starfish could be useful in managing these invasions.”



<h2 class="wp-block-heading" id="h-more-than-just-an-ancient-molecule">More than just an ancient molecule</h2>



This study connects two very different worlds: the sophisticated brain-gut interactions in humans and the slow, alien feeding behavior of starfish. Yet both rely on the same ancient molecule to know when it's time to stop eating.



As scientific discoveries reveal the biological links between species, the deep interconnectedness of all life becomes ever more apparent.



The full study was published in the journal <a href="https://dx.doi.org/10.1073/pnas.2420966122" target="_blank" rel="noreferrer noopener">Proceedings of the National Academy of Sciences</a>.



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Ancient molecule tells starfish and humans when to stop eating

The feeling of fullness after a nice meal usually prevents...

Humans are good at using the things that the natural world has to offer. Trees are used for their timber and fruits, bees and other insects pollinate our crops, and mountains bring us peace. But what happens when nature is pushed too far? 



As the planet heats up and extreme weather becomes more frequent, we may soon find ourselves counting the real cost - not just in lost trees or damaged trails, but in disappearing livelihoods and shaken communities.



Imagine Colorado’s wildflower meadows scorched by wildfire, or a strawberry field yielding less because heat drives away pollinators. These aren’t just <a href="https://www.earth.com/news/world-wildlife-day-2025-a-global-call-to-protect-nature/" target="_blank" rel="noreferrer noopener">environmental losses</a>; they impact economies, families, and entire ways of life. 



As extreme weather becomes more frequent, scientists are asking a new kind of question: How do we measure what we’re about to lose? A recent study led by <a href="https://www.colorado.edu" target="_blank" rel="noreferrer noopener">CU Boulder</a> researchers brings new tools to that conversation.



<h2 class="wp-block-heading" id="h-how-extreme-weather-harms-nature">How extreme weather harms nature</h2>



In a paper published in Nature Ecology &amp; Evolution, ecologist Laura Dee and her team introduced a computer model that looks at extreme weather with a fresh perspective.



The model connects environmental damage with economic and social consequences. It’s designed to predict what could happen if violent storms, fires, or floods hit ecosystems that people depend on.



The study’s example is striking: a forest in Minnesota could lose up to 50% of its timber income if a severe windstorm strikes.



“With climate change, there’s an urgent need to incorporate the impacts [that] extreme <a href="https://www.earth.com/news/people-must-reconnect-with-nature-now-to-save-biodiversity/" target="_blank" rel="noreferrer noopener">events</a> like mega-fires and hurricanes have on the benefits nature provides,” said Laura Dee, the paper’s first author and associate professor in the Department of Ecology and Evolutionary Biology.



“This research is an important step toward anticipating impacts to ecosystem services so that we can adapt management strategies accordingly.”



<h2 class="wp-block-heading" id="h-understanding-ecosystem-services">Understanding ecosystem services</h2>



The model focuses on what scientists call “ecosystem services,” which are the direct and indirect benefits that people derive from natural processes.



These include water purification by tree roots, crop pollination by insects, and carbon storage in <a href="https://www.earth.com/news/natures-grip-on-co2-is-slipping-what-it-means-for-us-all/" target="_blank" rel="noreferrer noopener">forests</a>. They also include less obvious values, like the joy of hiking or the cultural significance of a mountain lake.



Traditionally, climate models have treated environmental changes as gradual - things that happen slowly over time. But extreme weather doesn’t follow a smooth path. Wildfires, hurricanes, and floods hit fast and hard, causing damage that lingers long after the skies clear.



Dee’s model fills this gap by focusing on sudden disturbances and how they ripple through both ecosystems and economies. It doesn’t just track what gets damaged - it also accounts for how people value what is lost.



<h2 class="wp-block-heading" id="h-a-forest-put-to-the-test">A forest put to the test</h2>



To demonstrate how the model works, the researchers applied it to a mixed <a href="https://www.earth.com/news/we-must-live-in-harmony-with-nature-to-create-a-sustainable-future/" target="_blank" rel="noreferrer noopener">forest</a> in northern Minnesota. They studied how various tree species - each with different levels of wind resistance and market value - respond to intense windstorms.



For instance, white cedar trees are sturdy against strong winds but bring in less profit. Balsam firs are weaker but sell at a higher price.



The simulation showed a striking result: depending on storm strength, timber value could drop by between 23% and 50%. And timber isn’t the only thing at risk. Hiking, birdwatching, and camping opportunities also take a hit after such damage, further reducing the forest’s value to surrounding communities.



Dee said that researchers and land management officials could use the model to evaluate the impacts of any disturbances, from drought to invasive species.



<h2 class="wp-block-heading" id="h-reducing-extreme-weather-to-protect-nature">Reducing extreme weather to protect nature</h2>



Dee’s work doesn’t stop with predicting wind damage. Her research group at CU Boulder also looks at fire management. Specifically, they study how prescribed burns - intentional fires set under controlled conditions - can reduce wildfire <a href="https://www.earth.com/news/tackling-the-dual-crises-of-climate-and-nature/" target="_blank" rel="noreferrer noopener">risks</a>.



The new model supports these efforts by identifying areas where controlled burns could offer the greatest benefits. This includes not only reducing the risk of massive wildfires but also protecting other ecosystem services like clean water and carbon removal.



“Nature’s contributions to people have not typically been valued and are usually left out of key decision-making processes when developing land management policies and strategies,” Dee said.



By offering a clearer picture of what’s at stake, this model helps planners make smarter choices about which lands to protect and how.



<h2 class="wp-block-heading" id="h-a-wake-up-call-for-economic-systems">A wake-up call for economic systems</h2>



This isn’t just about trees and trails. It’s about how we prepare for a future where nature’s disruptions affect jobs, housing, and national economies. 



On March 5, the United Nations’ World Meteorological Organization reported that over 150 record-breaking weather events occurred across the globe last year. The pattern is not only repeating - it’s accelerating.



Dee believes our economic models must change to reflect this new reality. Traditional indicators like Gross Domestic Product don’t account for the value of clean air, stable forests, or functioning watersheds. But as these systems grow more vulnerable, leaving them out of the equation could become a costly mistake.



“If we fail to consider the growing risks from extreme weather events, we could lose more than we realize,” she said.



<h2 class="wp-block-heading" id="h-the-value-of-nature">The value of nature </h2>



What if planning for the future required not just spreadsheets and projections, but listening more closely to forests, rivers, and skies? Dee’s model is a reminder that nature’s value goes far beyond dollars. 



When we account for it properly, we make better decisions - not just for the environment, but for ourselves.



Extreme weather doesn’t wait. It strikes hard and fast. And with tools like this new simulation, we can at least be ready to measure the fallout and prepare. Because in the age of climate uncertainty, knowing what we stand to lose is the first step in making sure we don’t lose it.



The study is published in the journal <a href="https://www.nature.com/articles/s41559-024-02626-y" target="_blank" rel="noreferrer noopener">Nature Ecology &amp; Evolution</a>.



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Extreme weather is pushing nature toward a breaking point

Humans are good at using the things that the natural...

In a major scientific milestone, a team of researchers has captured the first continuous, real-time footage of cellulose being synthesized and self-assembled into the intricate scaffolding that gives plant cells their structure.&nbsp;



Using advanced microscopy techniques and a custom-built imaging system, the team recorded 24 hours of this cellular construction process in living plant cells, revealing surprising new details about how plant cell walls are built.



The study, led by <a href="https://newbrunswick.rutgers.edu/" target="_blank" rel="noreferrer noopener">Rutgers University–New Brunswick</a>, provides an unprecedented look into the behavior of cellulose - the most abundant biopolymer on Earth.



The research also offers insights that could lead to stronger, more resilient <a href="https://www.earth.com/news/nanoparticles-unlock-a-new-way-to-genetically-modify-plants/" target="_blank" rel="noreferrer noopener">crops</a>, cheaper biofuels, biodegradable plastics, and other sustainable products.



<h2 class="wp-block-heading" id="h-closer-look-at-plant-cells">Closer look at plant cells</h2>



Cellulose is a key component of plant cell walls and plays a vital role in maintaining plant structure. It’s also a valuable resource used in countless everyday products, from paper and clothing to food thickeners and filtration materials.



Sang-Hyuk Lee is an associate professor in the Department of Physics and Astronomy at Rutgers and a co-author of the study.&nbsp;



“This work is the first direct visualization of how cellulose synthesizes and self-assembles into a dense fibril network on a plant cell surface, since Robert Hook’s first microscopic observation of cell walls in 1667,” said Lee.



“This study also provides entirely new insights into how simple, basic physical mechanisms such as diffusion and self-organization may lead to the formation of complex cellulose networks in cells.”



The <a href="https://www.eurekalert.org/multimedia/1064673" target="_blank" rel="noreferrer noopener">videos</a> produced by Lee’s team show protoplasts - plant cells with their outer walls removed - from Arabidopsis, a relative of cabbage, as they spontaneously begin forming cellulose filaments.



These filaments grow outward from the cell surface in seemingly chaotic patterns, gradually coalescing into the highly organized structure of a new cell wall.



“I was very surprised by the emergence of ordered structures out of the chaotic dance of molecules when I first saw these video images,” Lee said. “I thought plant cellulose would be made in a lot more of an organized fashion, as depicted in classical biology textbooks.”



<h2 class="wp-block-heading" id="h-a-team-effort-across-disciplines">A team effort across disciplines</h2>



The breakthrough is the result of more than six years of collaboration between three Rutgers laboratories representing physics, engineering, and plant biology. Each group played a vital role in bringing the project to life.



When standard laboratory microscopes proved too limited to observe the fine detail of cellulose formation, Lee developed a specialized system based on total internal reflection fluorescence microscopy. 



This method allowed the researchers to image the cell’s underside with high resolution over long periods without damaging the samples.



Meanwhile, Shishir Chundawat, an associate professor in the Department of Chemical and Biochemical Engineering at Rutgers, led the development of a fluorescent probe system that tagged cellulose molecules so they could be visualized under the microscope. 



<h2 class="wp-block-heading" id="h-how-to-watch-plants-build-cell-walls">How to watch plants build cell walls</h2>



His team used a modified bacterial enzyme that binds specifically to cellulose to create the tagging system.



“I have always been fascinated by plants and how they capture sunlight via leaves into reduced carbon forms like cellulose that form cell walls,” said Chundawat, who is also focused on biofuel and bioproduct development. 



“I was inspired by collecting leaves as a middle school student. That early curiosity led me to delve deeper into biomass and its potential to create valuable, sustainable products.”



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/03/plant-cellulose_microfibril-network_illustration_credit-Ehsan-Faridi_1m.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/03/plant-cellulose_microfibril-network_illustration_credit-Ehsan-Faridi_1s.webp" alt="Artistic rendering of cellulose regenerating on a plant protoplast cell surface with zoomed out view. Cellulose is synthesized by plasma membrane-bound enzyme complexes (green) and assembles into a microfibril network (brown), forming the main scaffold for the cell wall. Credit: Ehsan Faridi/ Inmywork Studio/ Chundawat, Lee and Lam Labs" class="wp-image-1963291"/></a><figcaption class="wp-element-caption">Artistic rendering of cellulose regenerating on a plant protoplast cell surface with zoomed out view. Cellulose is synthesized by plasma membrane-bound enzyme complexes (green) and assembles into a microfibril network (brown), forming the main scaffold for the cell wall. Credit: Ehsan Faridi/ Inmywork Studio/ Chundawat, Lee and Lam Labs</figcaption></figure>



Eric Lam, a professor in the Department of Plant Biology, and his team developed the protocol to isolate protoplasts - cells stripped of their original walls. 



This provided a clean slate on which new cellulose fibers could be tracked as they formed in real time.



“This provided little to no background cellulose to confound our visualization and tracking of newly synthesized cellulose under optimized conditions,” Lam explained.



<h2 class="wp-block-heading" id="h-implications-for-agriculture-and-biofuels">Implications for agriculture and biofuels</h2>



The new findings are expected to inform future genetic and biotechnological efforts to enhance cellulose production in crops - improving traits like <a href="https://www.earth.com/news/droughts-and-extreme-weather-events-are-escalating/" target="_blank" rel="noreferrer noopener">drought</a> resistance, <a href="https://www.earth.com/news/turning-plants-into-carbon-capture-machines-with-cyanobacteria/" target="_blank" rel="noreferrer noopener">carbon capture</a>, and the efficiency of biomass conversion to fuel.



“This discovery opens the door for researchers to begin dissecting the genes that could play various roles for cellulose biosynthesis in the plant,” Lam said.&nbsp;



“The knowledge gained from these future studies will provide new clues for approaches to design better plants for carbon capture, improve tolerance to all kinds of environmental stresses, from drought to disease, and optimize second-generation cellulosic biofuels production.”



<h2 class="wp-block-heading" id="h-a-new-chapter-in-plant-biology">A new chapter in plant biology</h2>



The Rutgers team’s work challenges the traditional textbook narrative of orderly cellulose assembly, showing that what appears initially as disordered movement eventually organizes into the essential structure of the cell wall. 



This finding adds complexity to our understanding of plant biology and could inspire future scientists to take a closer look - literally and figuratively - at the hidden processes that sustain life on Earth.



Animations aimed at young students often simplify how plant cell walls are made, but the Rutgers team’s research reveals that the real process is far more intricate - and far more beautiful.



The study is published in the journal <a href="http://dx.doi.org/10.1126/sciadv.ads6312" target="_blank" rel="noreferrer noopener">Science Advances</a>.



Image Credit: Ehsan Faridi/ Inmywork Studio/ Chundawat, Lee and Lam Labs



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How plants build their cell walls is seen by scientists for the first time ever

In a major scientific milestone, a team of researchers has...

It's easy to think that older forests, with their diverse and well established trees, are better at storing carbon. Many assume that, as trees grow and ecosystems mature, they naturally become more effective at soaking up carbon from the atmosphere. 



A new study from scientists at the <a href="https://umich.edu/" target="_blank" rel="noreferrer noopener">University of Michigan</a> Biological Station challenges this assumption, however, and suggests that the reality is much more complicated.



The research team, which included more than 100 scientists over several decades, found that <a href="https://www.earth.com/news/mixed-forests-with-many-tree-species-are-more-effective-at-carbon-storage/" target="_blank" rel="noreferrer noopener">carbon storage in forests</a> depends more on what's happening within the ecosystem than how old it is. 



Factors like the structure of the forest canopy, the types of trees and fungi present, and how nutrients move through the soil all play a bigger role than previously thought.



<h2 class="wp-block-heading" id="h-looking-at-two-centuries-of-change">Looking at two centuries of change</h2>



The research was conducted at the U-M Biological Station in Pellston, Michigan. This historic field site, founded in 1909, spans over 10,000 acres and has long served as a hub for studying northern <a href="https://www.earth.com/news/forests-rich-tree-diversity-adapt-better-changing-climate/" target="_blank" rel="noreferrer noopener">forest ecosystems</a>. 



Scientists used data from a wide range of forest stands on the property. Some were untouched remnants from the 1800s, while others had been logged or burned at different points in the 20th century.



At the heart of the study was a massive dataset that had been built over decades. It included information from the station’s 150-foot AmeriFlux tower, which tracks carbon dioxide, water, and energy flows between forests and the atmosphere.



Additional data covered everything from soil respiration and microbial activity to leaf litter, root growth, and nutrient cycling.



Luke Nave was the study's lead researcher and a faculty member at Michigan Technological University.



"Time is not what drives <a href="https://www.earth.com/news/plants-release-carbon-faster-than-we-expected/" target="_blank" rel="noreferrer noopener">carbon cycling</a>," said Nave. "Time is more of a playing field, and the rules of the game on that field are things like canopy structure, tree and microbial community composition, and soil nitrogen availability."



"That means that changes in things like structure, composition and soil nitrogen are what control forest carbon trajectories, whether those changes happen quickly or slowly, and whether we are influencing those changes through management or letting them happen on their own terms."



<h2 class="wp-block-heading" id="h-the-power-of-long-term-carbon-research">The power of long-term carbon research</h2>



One of the study’s strengths lies in its use of both historical and current data. 



With so much emphasis on real-time monitoring, the researchers were able to paint a detailed picture of how carbon moves through forest ecosystems - and how that movement has changed over time.



"It's exciting to see the results of this study. It was a lot of work and many years in the making," said Jason Tallant, data manager and research specialist at the University of Michigan Biological Station.



"At the U-M Biological Station, we put a lot of effort into data curation and digitization. It's nice to see the carbon synthesis research team leverage our historic data sets and crunch real-time <a href="https://www.earth.com/news/forest-modeling-study-reveals-new-insights-into-carbon-sequestration/" target="_blank" rel="noreferrer noopener">carbon sequestration</a> information to illuminate what's happening in our forests and inform future management."



The project brought together a wide range of measurements, including fungal community studies, root production, carbon pool tracking, and soil enzyme activity. All of these factors helped the team understand how different pieces of the ecosystem influence carbon storage.



<h2 class="wp-block-heading" id="h-rethinking-forest-management">Rethinking forest management</h2>



The takeaway from this study is clear: managing forests means more than just letting them grow old. 



If we want forests to help mitigate climate change, we need to pay close attention to their structure and species makeup, both above and below the ground.



"With the rates of change we're now seeing in things like climate, forest health and disturbance, and tree species composition, management will have to contend with more challenges and constraints all the time. What was true a decade or two ago can't be assumed as truth at this point," Nave commented.



"A good example for folks who know the territory is on the Burn Plots - the 1998 burn is a thriving young stand of post-clearcut aspen, and the 2017 burn is a regeneration failure. You might not think that 19 years is a long time to a tree, but it is in today's world."



"Researchers and managers who take a whole-ecosystem perspective like we did in the paper will have an easier time understanding what has changed over the last few decades and what we can do about it to <a href="https://www.earth.com/news/future-forests-which-tree-species-can-survive-climate-change/" target="_blank" rel="noreferrer noopener">sustain forests</a>."



This study reminds us that forests are dynamic systems, and treating them as such is essential for their health and their ability to store carbon. 



Simply counting the years isn't enough. Understanding what happens within those years is what really matters.



The full study was published in the journal <a href="https://esajournals.onlinelibrary.wiley.com/doi/10.1002/eap.70001">Ecological Applications</a>.



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Older forests do not necessarily store more carbon

It's easy to think that older forests, with their diverse...

Pregnancy often brings with it a mix of anticipation, anxiety, and countless decisions - especially about food. For decades, health experts have promoted beans as a budget-friendly powerhouse food rich in protein, fiber, and complex carbohydrates. 



Now, new research offers an interesting twist: eating chili with beans during pregnancy may reduce the risk of developing gestational diabetes.



This spicy finding comes from a recent study by researchers at the University at Buffalo. Published in the journal Nutrients, the study highlights chili as a possible dietary ally for <a href="https://www.earth.com/news/study-links-teen-pregnancy-to-smaller-newborns/" target="_blank" rel="noreferrer noopener">pregnant individuals</a> - especially those at higher risk for blood sugar complications.



But how did the researchers make this connection? And why chili, specifically? The answers may surprise you.



<h2 class="wp-block-heading" id="h-rising-challenge-of-gestational-diabetes">Rising challenge of gestational diabetes</h2>



Gestational diabetes is a condition diagnosed during pregnancy that affects how the body processes sugar.



If unmanaged, it can lead to complications for both the baby and the mother. While the condition typically resolves after childbirth, it leaves behind a lingering risk - mothers are more likely to develop Type 2 diabetes later in life.



Factors like pre-pregnancy obesity, maternal age, excessive pregnancy weight gain, low physical activity, poor diet, and even COVID-19 have all been linked to this condition. 



​According to recent data from the&nbsp;<a href="https://www.cdc.gov/mmwr/volumes/72/wr/mm7201a4.htm" target="_blank" rel="noreferrer noopener">Centers for Disease Control and Prevention</a>, gestational diabetes in the U.S. increased from 6.0% in 2016 to 8.3% in 2021.​



In response to this rise, researchers are exploring ways to reduce risk - ideally through practical, nutritional choices. That’s where beans come into the picture.



Known for their ability to stabilize blood sugar levels and support digestive health, beans have already earned their place on many healthy-eating lists. But what happens when beans are cooked into a spicy, flavorful bowl of chili?



<h2 class="wp-block-heading" id="h-chili-consumption-during-pregnancy">Chili consumption during pregnancy </h2>



The team at the University at Buffalo wanted to explore this very question. 



Using data from the Infant Feeding Practices Study II, a U.S. national cohort effort by the Food and Drug Administration and the CDC, researchers analyzed eating habits of 1,397 pregnant women. 



Their goal was to see if different forms of bean consumption - chili, dried beans, and bean soup - had any effect on the risk of gestational diabetes during pregnancy.



“Our research aimed to study the roles of bean consumption in gestational diabetes, including chili, dried beans and bean soup,” said Dr.&nbsp;Xiaozhong Wen, first author and associate professor of pediatrics in the Division of Behavioral Medicine in the&nbsp;<a href="https://medicine.buffalo.edu/" target="_blank" rel="noreferrer noopener">Jacobs School of Medicine and Biomedical Sciences</a>.​



“Interestingly, only chili consumption was statistically significantly associated with the risk of gestational diabetes.”



According to the study, <a href="https://www.earth.com/news/how-pregnancy-changes-the-brain/" target="_blank" rel="noreferrer noopener">women</a> who ate chili once per month had a 3.5% risk of developing gestational diabetes. Those who never ate chili had a 7.4% risk. That’s a significant difference for just one serving a month. 



But it also raises a new question: what makes chili so special?



<h2 class="wp-block-heading" id="h-chili-may-help-control-blood-sugar">Chili may help control blood sugar</h2>



Beans alone carry many benefits, including being high in fiber and low on the glycemic index. But chili often includes more than just beans. It typically contains dark beans, chili powder, and sometimes additional spices - all of which might contribute to its unique effects on blood sugar.



The researchers point to two specific components: capsaicin, the compound responsible for chili’s heat, and phenolic compounds found in dark beans. These substances have shown promise in both human and animal studies.



“Both human and animal studies have shown that capsaicin and phenolic compounds have some potential benefits of improving glycemic control through slowing glucose absorption and increasing insulin secretion and/or insulin sensitivity,” said Wen.



While the exact mechanism isn’t fully understood, the combination of these elements may work together to help the body manage blood sugar more effectively. This makes chili not just a comfort food but potentially a functional food - at least for <a href="https://www.earth.com/news/pregnancy-stress-may-have-lasting-effects-on-fetal-development/" target="_blank" rel="noreferrer noopener">pregnant women</a>.



<h2 class="wp-block-heading" id="h-future-research-on-chili-during-pregnancy">Future research on chili during pregnancy </h2>



It’s important to note that this study was observational. That means the researchers didn’t assign participants to eat chili; they simply studied existing eating patterns and health outcomes. As a result, they cannot prove cause and effect.



Wen acknowledges this and calls for caution when interpreting the findings. He emphasizes the need for further research.



Wen says the research findings need to be replicated in larger cohorts with more diverse populations, detailed measures of bean consumption and dietary intake information collected more frequently and a randomized controlled design.



He adds that given the non-causal nature of observational research, recall bias and selection bias, the findings should be interpreted cautiously.



That said, the results are compelling enough to encourage further investigation. A single monthly serving of chili cutting gestational diabetes risk nearly in half is an idea worth exploring, especially if it can be done safely and inexpensively.



<h2 class="wp-block-heading" id="h-chili-may-support-a-diabetes-safe-diet">Chili may support a diabetes-safe diet</h2>



So what should expecting mothers do with this information? Should chili become a regular part of prenatal nutrition? Wen offers a balanced approach.



“Moderate chili consumption may be incorporated into a balanced diet approach to addressing gestational diabetes, along with other clinical recommendations, such as early screening, diagnosis, exercise and medications as needed,” says Wen.



This means chili should not replace medical care or professional dietary advice, but it may have a place at the table. Especially for <a href="https://www.earth.com/news/moms-health-shapes-how-well-an-embryo-develops/" target="_blank" rel="noreferrer noopener">women</a> at higher risk of gestational diabetes, it could be a simple, delicious way to support their health.



<h2 class="wp-block-heading" id="h-looking-ahead-what-comes-next">Looking ahead: What comes next</h2>



​The study was co-led by Todd C. Rideout, PhD, associate professor of exercise and nutrition sciences in the&nbsp;<a href="https://publichealth.buffalo.edu/" target="_blank" rel="noreferrer noopener">School of Public Health and Health Professions</a>&nbsp;at the&nbsp;<a href="https://www.buffalo.edu/" target="_blank" rel="noreferrer noopener">University at Buffalo</a>.&nbsp;



Other University at Buffalo contributors included Fatima Makama, Ryan Buzby, Jeremy Nguyen, Rose Durnell, Iyobosa Ekhator, and Daren Chan.&nbsp;The&nbsp;<a href="https://www.usda.gov/" target="_blank" rel="noreferrer noopener">U.S. Department of Agriculture</a>&nbsp;funded the research.​



As scientists continue to explore the links between food and <a href="https://www.earth.com/news/cbd-use-during-pregnancy-has-unexpected-consequences/" target="_blank" rel="noreferrer noopener">maternal health</a>, this study opens new possibilities. A bowl of chili may hold more than warmth and flavor — it might also support better blood sugar control during one of life’s most critical periods.



For now, pregnant individuals should focus on balanced eating, regular checkups, and physical activity. But with research like this, even small choices — like what you put in your bowl — could make a meaningful difference.



The study is published in the journal <a href="https://www.mdpi.com/2072-6643/17/6/1025" target="_blank" rel="noreferrer noopener">Nutrients</a>.



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Eating chili during pregnancy may actually be a good idea

Pregnancy often brings with it a mix of anticipation, anxiety,...

In the invisible war between life forms, bacteria constantly fight off threats from viruses. These viruses, known as bacteriophages or simply “phages,” infect bacterial cells the same way human viruses attack our own bodies, leaving behind a memory of the invasion.



But unlike humans, bacteria don’t have white blood cells or antibodies. Instead, they use a genetic system called CRISPR to defend themselves. This ancient defense system is now drawing fresh attention from scientists.



Recent research from Johns Hopkins Medicine shows that <a href="https://www.earth.com/news/bacteria-strain-identified-that-can-eat-forever-chemicals/" target="_blank" rel="noreferrer noopener">bacteria</a> don’t just defend passively. They actively gather pieces of viral code to remember their enemies. They pass these memories to their descendants. 



Understanding this bacterial memory process may help us design new treatments for antibiotic-resistant infections - a growing global concern.



<h2 class="wp-block-heading" id="h-what-are-phages">What are phages?</h2>



Phages get their name from the Greek word meaning “bacteria-eaters.” 



These viruses either destroy their bacterial hosts or hide quietly inside them. That quiet phase is called dormancy. While dormant, the virus does not kill the host. Instead, it lives silently within the bacterial DNA.



Researchers have long wondered how <a href="https://www.earth.com/news/bacteria-pseudomonas-build-tiny-nano-spearguns-to-fight-back-against-attack/" target="_blank" rel="noreferrer noopener">bacteria</a> survive the first wave of viral infection, especially from these temperate phages. The answer may lie in how bacteria collect and store genetic fragments from dormant viruses. 



This behavior is not just survival; it's preparation for the future.



<h2 class="wp-block-heading" id="h-biological-memory-of-viruses">Biological memory of viruses</h2>



In the Johns Hopkins study, researchers focused on Streptococcus pyogenes, the bacteria responsible for strep throat. They found that these bacteria take advantage of temperate phages during their inactive phase. 



The bacteria gather genetic information from the phage while it’s dormant. This material forms a biological “memory” of the invader.



As the bacteria multiply, they pass this memory on. That means future generations are born with a built-in recognition system. When the same phage attacks again, the <a href="https://www.earth.com/news/bacteria-pseudomonas-build-tiny-nano-spearguns-to-fight-back-against-attack/" target="_blank" rel="noreferrer noopener">bacterial descendants</a> already know how to defend themselves.



“We essentially wanted to answer the question: If bacterial cells don’t have any memory, or survival skills, to combat a new temperate phage that shows up, how do they buy themselves enough time to establish a new memory, before they succumb to that initial infection?” said Modell.



<h2 class="wp-block-heading" id="h-bacteria-use-crispr-to-store-viral-memory">Bacteria use CRISPR to store viral memory</h2>



Bacteria use the CRISPR-Cas system to deal with phages. This system stores DNA from previous infections. When a known phage tries to re-enter, CRISPR recognizes its genetic material and destroys it.



Johns Hopkins researchers infected <a href="https://www.earth.com/news/bacteria-and-imprint-new-era-dna-transformation/" target="_blank" rel="noreferrer noopener">bacterial cells</a> with both natural phages that go dormant and genetically modified phages that stay active. They wanted to see how the CRISPR system responded under both conditions.



“Our results indicate that the bacteria’s CRISPR system was more effective at using the naturally dormant phage to pull parts of the viral genetic code into their genome,” said Modell. “When we tested phages that could not go dormant, the CRISPR system did not work nearly as well.”



<h2 class="wp-block-heading" id="h-dormant-viruses-boost-bacteria-memory">Dormant viruses boost bacteria memory</h2>



When phages go dormant, bacteria have more time. They use this period to build memory and prepare defenses. Researchers then allowed the surviving bacteria to multiply. They sequenced the DNA of these new generations.



The results were striking. The bacteria had collected hundreds of thousands of genetic “memories.” Each entry in the CRISPR system reflected past encounters with the virus. This memory-building happened mostly during dormancy, when the virus posed no immediate threat.



“This is conceptually similar to a vaccine with an attenuated virus,” said Nicholas Keith, a graduate student and first author of the paper.



“We believe this is the reason why the CRISPR Cas9 system has a unique <a href="https://www.earth.com/news/hungry-bacteria-will-devour-plastic-waste/" target="_blank" rel="noreferrer noopener">relationship</a> with this specific class of temperate phage.”



<h2 class="wp-block-heading" id="h-understanding-how-the-system-works">Understanding how the system works </h2>



Vaccines train human immune systems by introducing harmless versions of dangerous viruses. The CRISPR system appears to do something similar. Dormant phages act like training tools, helping bacteria prepare without putting their survival at risk.



“We can use these types of experiments to find what elements of the phage, the bacterial host and its CRISPR system are important for all stages of bacterial immunity,” explained Keith.



Researchers are especially interested in why the system works better with dormant viruses than with active ones. This information could shape how scientists use phages to treat bacterial infections in humans.



<h2 class="wp-block-heading" id="h-future-treatments-and-fighting-resistance">Future treatments and fighting resistance</h2>



Antibiotic resistance is a growing problem. Some bacterial infections no longer respond to any known drugs. Phage therapy - using viruses to attack <a href="https://www.earth.com/news/how-bacteria-share-genes-and-defy-defenses/" target="_blank" rel="noreferrer noopener">bacteria</a> - is one potential solution. But this approach only works if we understand how bacteria defend themselves.



“We know CRISPR systems are one of the first lines of defense against the transfer of hazardous genes from phages that turn bacterial cells toxic. Furthermore, our studies will inform the design of ‘phage therapies’ which could be used in clinical cases where a bacterial infection is resistant to all available antibiotics,” noted Modell.



Understanding CRISPR could help scientists fine-tune phage therapies. They could choose or design viruses that bacteria are less able to resist, leading to more effective treatments.



<h2 class="wp-block-heading" id="h-a-collaborative-effort">A collaborative effort</h2>



​The research was supported by multiple institutions, including the&nbsp;<a href="https://www.hopkinsmedicine.org/som/" target="_blank" rel="noreferrer noopener">Johns Hopkins University School of Medicine</a>, the&nbsp;<a href="https://www.nih.gov/" target="_blank" rel="noreferrer noopener">National Institutes of Health</a>, the&nbsp;<a href="https://ritaallen.org/" target="_blank" rel="noreferrer noopener">Rita Allen Foundation</a>, and the&nbsp;<a href="https://www.nsf.gov/" target="_blank" rel="noreferrer noopener">National Science Foundation</a>.​



In addition to Nicholas Keith and Joshua Modell, the team included Rhett Snyder from Johns Hopkins and Chad Euler from <a href="https://hunter.cuny.edu" target="_blank" rel="noreferrer noopener">Hunter College</a>. Their combined efforts push us closer to smarter, safer ways of managing infections that resist current drugs.



In the end, studying bacteria doesn’t just teach us about microbes. It shows us new paths to protect ourselves, using lessons written in the smallest pieces of life.



The study is published in the journal <a href="https://www.cell.com/cell-host-microbe/fulltext/S1931-3128(25)00029-0" target="_blank" rel="noreferrer noopener">Cell Host &amp; Microbe</a>.



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Bacteria pass down their memories to fight viruses

In the invisible war between life forms, bacteria constantly fight...

When stars are born, they often release powerful jets that carve dramatic trails through space. The&nbsp;James Webb Space Telescope, a collaboration between&nbsp;<a href="https://www.nasa.gov/" target="_blank" rel="noreferrer noopener">NASA</a>,&nbsp;<a href="https://www.esa.int/" target="_blank" rel="noreferrer noopener">ESA</a>, and&nbsp;<a href="https://www.csagroup.org/" target="_blank" rel="noreferrer noopener">CSA</a>, recently captured a stunning example.



In this image, a young star’s jet - known as Herbig-Haro 49/50 - appears alongside a perfectly aligned distant spiral galaxy. Together, they create a visual that appears both staged and surreal.



The power of <a href="https://science.nasa.gov/mission/webb/" target="_blank" rel="noreferrer noopener">Webb</a> lies not only in what it sees but in how it sees. With advanced infrared vision, it unveils details that were once lost in cosmic fog. In this image, what looks like a tornado of glowing material winds through the <a href="https://www.earth.com/news/four-small-planets-discovered-orbiting-the-nearest-single-star-to-earth-barnards-star/" target="_blank" rel="noreferrer noopener">darkness</a>. 



But this is not mere chaos - this is a structured flow of matter from a forming star. The scene is a fusion of science and art, and the alignment of two unrelated cosmic objects gives the image a unique depth.



<h2 class="wp-block-heading" id="h-how-baby-stars-launch-wild-jets">How baby stars launch wild jets</h2>



Herbig-Haro objects form during the earliest stages of <a href="https://www.earth.com/news/runaway-star-may-be-dragging-a-planet-along-with-it/" target="_blank" rel="noreferrer noopener">star</a> formation. Young stars, still gathering mass, often shoot out narrow jets of gas. These jets crash into the surrounding material, heating it up. As the heated gas cools, it emits light that astronomers can detect in visible and infrared wavelengths.



HH 49/50, located about 630 light-years from Earth in the Chamaeleon constellation, is a classic example. This region is among the closest active star-forming areas in our galaxy. 



​The&nbsp;James Webb Space Telescope&nbsp;utilized both its&nbsp;Near-Infrared Camera (<a href="https://science.nasa.gov/mission/webb/nircam/" target="_blank" rel="noreferrer noopener">NIRCam</a>)&nbsp;and&nbsp;Mid-Infrared Instrument (<a href="https://science.nasa.gov/mission/webb/mid-infrared-instrument-miri/" target="_blank" rel="noreferrer noopener">MIRI</a>)to produce a layered, high-resolution image.&nbsp;This composite allows scientists to examine small-scale details with unprecedented clarity.



This level of detail is vital for studying the birthplaces of stars like our Sun. These jets don’t just travel quietly - they plow through surrounding clouds, forming shock waves and reshaping the <a href="https://www.earth.com/news/fluffy-molecular-clouds-may-change-our-understanding-of-star-formation/" target="_blank" rel="noreferrer noopener">cosmic</a> landscape.



<h2 class="wp-block-heading" id="h-a-tornado-in-space">A tornado in space</h2>



When NASA’s Spitzer Space Telescope first observed HH 49/50 in 2006, scientists were intrigued by its spiral, storm-like shape. 



They nicknamed it the "Cosmic Tornado" because of its swirling, helical appearance. However, Spitzer couldn’t resolve the fine structures clearly. A fuzzy patch at the tip of the outflow remained a mystery.



Now, Webb’s resolution changes everything. It reveals that the fuzzy patch is not a continuation of the jet, but a distant spiral galaxy. Its structure is crisp and distinct. 



This unexpected discovery highlights the telescope’s ability to separate overlapping layers of cosmic material and isolate individual objects, even in <a href="https://www.earth.com/news/star-formation-reignited-in-the-galaxy-leo-p-after-billions-of-years/" target="_blank" rel="noreferrer noopener">complex environments</a>.



The galaxy, seen face-on, lies far beyond HH 49/50. But the illusion of connection adds wonder. In the background, countless other galaxies fill the scene. Webb has, by chance, framed a dynamic, turbulent jet against a calm, elegant spiral structure.



<h2 class="wp-block-heading" id="h-a-nursery-for-young-stars">A nursery for young stars</h2>



HH 49/50 resides within the Chamaeleon I Cloud complex. This region serves as a stellar nursery, busy with the birth of low-mass stars. It closely resembles the type of place where our own Sun likely formed. 



The outflow from HH 49/50 is moving at blazing speeds - between 100 and 300 kilometers per second. Yet it’s only part of a larger network of outflows sculpting the cloud.



By examining the light from the object, scientists trace glowing hydrogen and carbon monoxide molecules, along with energized dust grains. These materials appear as brilliant orange and red streaks in the image. Their location and movement reveal how the outflow is reshaping its <a href="https://www.earth.com/news/six-planet-system-hd110067-discovered-that-moves-in-perfect-mathematical-harmony/" target="_blank" rel="noreferrer noopener">environment</a>.



The Webb data also shows arcs that resemble the wake left by a speeding boat. These arc-shaped features help astronomers trace the flow’s direction and better understand its dynamics. Each curve and twist in the material tells a story of energy, motion, and cosmic change.



<h2 class="wp-block-heading" id="h-chasing-the-source-of-the-jet">Chasing the source of the jet</h2>



To understand what powers such a dramatic outflow, astronomers look toward its possible source. Evidence points to a young protostar named Cederblad 110 IRS4, or CED 110 IRS4. 



This object lies about 1.5 light-years away from HH 49/50, just off the edge of Webb’s main image. It’s considered a Class I protostar, meaning it’s still actively gathering mass and developing.



Class I protostars typically have surrounding disks of gas and dust. These disks slowly feed the growing star, and jets often emerge as a by-product of this process. 



Webb’s instruments helped scientists examine CED 110 IRS4 in detail, revealing the icy material in its surroundings. This kind of analysis helps build a more complete picture of the early stages of stellar evolution.



While most arcs point back to this protostar, not all align perfectly. That discrepancy invites new questions and adds complexity to the scene.



<h2 class="wp-block-heading" id="h-why-is-the-star-jet-so-messy">Why is the star jet so messy?</h2>



Some features within HH 49/50 seem out of place. A distinct outcrop in the upper right corner of the image may hint at another outflow. 



One possibility is that it belongs to a separate jet overlapping the main one. Another idea is that it results from the main jet’s shifting direction - a process called precession.



Jet precession can happen when the protostar wobbles or experiences changes in its environment. Over time, this causes the outflow to twist and shift, creating multiple arcs that point in slightly different directions. Alternatively, the feature might be caused by the jet breaking apart as it interacts with nearby clouds.



Such findings reveal the limits of current models and show that nature doesn’t always follow simple rules. Every new observation from Webb introduces new variables to consider.



<h2 class="wp-block-heading" id="h-a-spiral-galaxy-in-perfect-position">A spiral galaxy in perfect position</h2>



The spiral galaxy near the tip of HH 49/50 seems almost too perfectly placed. It’s a coincidence of cosmic alignment. 



The galaxy is not physically related to the outflow, but the visual juxtaposition creates a powerful image. Its face-on orientation displays a glowing central bulge, which appears blue. This region contains older stars.



The spiral arms stretch outward, peppered with reddish clumps of warm dust and active star formation. These features are not unique to this galaxy. Similar bubbles and dust pockets have been observed in other nearby galaxies using Webb, especially through the <a href="https://sites.google.com/view/phangs/home" target="_blank" rel="noreferrer noopener">PHANGS program</a>.



This comparison allows astronomers to draw parallels between our galactic neighborhood and more distant systems. And while the galaxy itself sits far beyond HH 49/50, its presence enriches the image with depth and contrast.



<h2 class="wp-block-heading" id="h-distant-galaxy-meets-a-star-jet">Distant galaxy meets a star jet</h2>



Webb’s image of HH 49/50 and the distant spiral galaxy captures a rare alignment. 



Over thousands of years, the outflow will expand and eventually obscure the galaxy behind it. This brief window gives astronomers a unique perspective - one that won’t last forever.



The beauty of the cosmos lies in both motion and stillness. Webb, with its unmatched vision, freezes this cosmic dance in perfect clarity. The resulting image is not just science - it’s a moment of wonder. A look into a turbulent birthplace of stars framed against the silent rotation of a distant galaxy.



Image Credit: James Webb Space Telescope.



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Cosmic Tornado: A young star’s jet collides with space dust

When stars are born, they often release powerful jets that...

Latimeria,Fish,Isolated,On,The,Black,Background

Among the many wonders and ancient tales about marine life and ocean creatures, one fish long believed to have vanished from our planet captured worldwide attention. 



This interest emerged from an unexpected finding that changed our perspective on what might still be lurking in the deep.



Before 1938, experts spoke of the coelacanth as a classic example of an extinct fish dating back more than 400 million years. Scholars concluded it had disappeared 65 to 70 million years ago. 



This assumption crumbled when a 32-year-old museum employee in East London, South Africa, examined a strange specimen brought by a local fisherman near the Chalumna River. The fish defied every existing category she knew.



Soon after, she contacted <a href="https://en.wikipedia.org/wiki/J._L._B._Smith" target="_blank" rel="noreferrer noopener">Professor James Leonard Brierley Smith</a> of <a href="https://www.ru.ac.za/" target="_blank" rel="noreferrer noopener">Rhodes University</a> for advice. He confirmed that the fish was indeed a living coelacanth. 



That surprise discovery shifted the zoological narrative and demonstrated how the fossil record can be incomplete, especially when only a small number of individuals survive.



<h2 class="wp-block-heading" id="h-fascinating-fish-tale">Fascinating fish tale</h2>



In the eyes of many scientists, the coelacanth’s resurgence placed it into what is called a Lazarus taxon. The term refers to creatures that vanish from evidence, then reappear without warning. 



One telling moment from that occasion remains the telegram from Brierley Smith: “MOST IMPORTANT PRESERVE SKELETON AND GILLS = FISH DESCRIBED.” 



No one anticipated those words, yet they confirmed something rare had surfaced.



After that event, more than a decade passed before another coelacanth turned up. In 1952, two fishermen in the Comoro Islands accidentally netted the second specimen, prompting renewed fascination among marine researchers. 



A further revelation followed in the 1990s, when experts identified a second species around the Indonesian archipelago. 



These examples carry the names <a href="https://www.earth.com/news/asian-megacities-at-highest-risk-from-sea-level-rise/" target="_blank" rel="noreferrer noopener">West Indian Ocean</a> coelacanth (Latimeria chalumnae) and Indonesian coelacanth (Latimeria menadoensis).



<h2 class="wp-block-heading" id="h-coelacanth-has-unique-physical-traits">Coelacanth has unique physical traits</h2>



This fish stands apart for its lobed pectoral fins, which appear to be an early link to vertebrates that eventually ventured onto land. These fins move in a synchronized pattern, allowing the fish to navigate underwater terrains. 



Unlike many other fishes, it also bears an unusual hinge in its skull, once a subject of speculation about how it might bite or process food.



Its coloration often blends with the rocky surroundings where it resides, offering a measure of cover in deep marine environments. 



The habitat provides sufficient shelter from predators, while the species’ low metabolism helps it survive on fewer resources. 



Scientists note that it rests in lava-cave recesses during daylight hours, an approach that likely shields it from hazards in open water.



<h2 class="wp-block-heading" id="h-ancestral-ties-to-land-creatures">Ancestral ties to land creatures</h2>



Researchers classify the coelacanth under the <a href="https://www.earth.com/news/mysterious-fish-like-fossil-finally-classified/" target="_blank" rel="noreferrer noopener">group Sarcopterygii</a>, or lobe-finned fishes, which include lungfish and the earliest ancestors of amphibians, reptiles, and mammals. 



Shared skeletal features, such as sturdy fin bones, point to a closer relationship with organisms that adapted to life on land. 



This connection is intriguing because it shows how certain aquatic traits can mirror structures later found in creatures roaming dry terrain.



Some studies suggest that the coelacanth’s rostral organ, located in its snout, may sense electrical signals from prey. 



That adaptation is reminiscent of strategies seen in other <a href="https://www.earth.com/news/coelacanth-ngamugawi-wirngarri-new-species-living-fossil-fish-survived-over-400-million-years/" target="_blank" rel="noreferrer noopener">lobe-finned fish</a>, hinting at a link between modern species and those that made their way onto shore millions of years ago. 



Observers note that this hidden ability emphasizes how an ancient design can remain effective.



<h2 class="wp-block-heading" id="h-geological-stability-has-helped-coelacanths">Geological stability has helped coelacanths</h2>



The ancient environment of undersea caverns has changed little over vast stretches of time. 



Because of this stable setting, the coelacanth has not faced the intense pressures that other species might encounter in rapidly shifting habitats. 



Food sources may be limited, but the fish’s slow pace lessens its caloric needs.



Its specialized niche also guards it from fierce competition. Other oceanic predators seldom patrol these dark, quiet zones, giving the coelacanth space to endure without altering the basic features that first appeared centuries ago. 



This alignment between organism and setting reveals a powerful strategy: remain where the external world barely intrudes.



<h2 class="wp-block-heading" id="h-inspiring-story-of-adaptation-and-survival">Inspiring story of adaptation and survival</h2>



Many living forms adapt constantly to survive. By contrast, this fish’s story underscores how a creature can persist if external demands remain light and internal physiology fits the available conditions. 



Though it caused surprise among zoologists, the coelacanth itself quietly continued in an environment well-suited to its capabilities.



To many observers, it sparks discussions on biodiversity and the surprising ways life endures. While others might call it a relic, it is very much a survivor. 



Each sighting encourages experts to keep watching the deep sea, a region that may hold additional beings we once wrote off as extinct.



Scientists continue to investigate whether this fish harbors undiscovered traits. Each observation can add to our understanding of marine evolution. 



Observers hope that further study might shed new light on adaptations that remain hidden in dark, remote corners of the ocean.



The full study was published in the journal <a href="https://www.nature.com/articles/s41598-023-37849-9" target="_blank" rel="noreferrer noopener">Scientific Reports</a>.



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World’s oldest fish was presumed extinct for 60 million years before being rediscovered

Among the many wonders and ancient tales about marine life...

The past is full of hidden secrets, and fossils offer valuable glimpses into ancient worlds. Each discovery reveals new insights into evolution, extinction, and the environmental shifts that shaped life long ago.



A recent study on a 30,000-year-old vulture fossil from Central Italy has revealed an extraordinary process of preservation. 



The researchers discovered that volcanic rock can capture microscopic details of feathers - a phenomenon that has never been documented before.



Fossilization usually occurs in sediments like mud or sand, where minerals replace organic materials over time. 



However, the vulture <a href="https://www.earth.com/news/organic-molecules-collagen-discovered-in-66-million-year-old-dinosaur-bones/" target="_blank" rel="noreferrer noopener">fossil</a> challenges conventional beliefs by showing how volcanic deposits can preserve soft tissues in stunning detail.



<h2 class="wp-block-heading" id="h-30-000-year-old-vulture-fossil">30,000-year-old vulture fossil</h2>



The fossilized vulture was discovered in 1889 near Rome by a local landowner. Its exceptional state of preservation made it a rare find at the time.



Unlike many <a href="https://www.earth.com/news/triassic-fossils-shed-new-light-on-ancient-ecosystems/" target="_blank" rel="noreferrer noopener">fossils</a> that are flattened by geological pressure, this specimen retained a three-dimensional structure. Even features like eyelids and wing feathers remained intact.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/03/vulture-fossil-feather_volcanic-rock_credit-Edoardo-Terranova_1m.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/03/vulture-fossil-feather_volcanic-rock_credit-Edoardo-Terranova_1s.webp" alt="A Fossilized feather preserved with the volcanic rock. Credit: Edoardo Terranova" class="wp-image-1963155"/></a><figcaption class="wp-element-caption">A Fossilized feather preserved with the volcanic rock. Credit: Edoardo Terranova</figcaption></figure>



Despite its discovery more than a century ago, the fossil has continued to fascinate researchers. Recent advances in microscopic and chemical analysis provided scientists with tools to examine it anew, this time in unprecedented detail.



The findings have opened new doors in the study of fossilization and volcanic environments.



<h2 class="wp-block-heading" id="h-feathers-preserved-at-the-microscopic-level">Feathers preserved at the microscopic level</h2>



Dr. Valentina Rossi from University College Cork led the research team that conducted a detailed examination of the vulture fossil. 



The results, published recently in Geology, reveal that the feathers are preserved down to the microscopic level.



“Fossil feathers are usually preserved in ancient mudrocks laid down in lakes or lagoons,” noted Dr. Rossi.



“The fossil vulture is preserved in ash deposits, which is extremely unusual. When analyzing the <a href="https://www.earth.com/news/neanderthal-fossils-reveal-signs-of-a-population-collapse/" target="_blank" rel="noreferrer noopener">fossil</a> vulture plumage, we found ourselves in uncharted territory. These feathers are nothing like what we usually see in other fossils.”



Traditional fossilization often occurs in water-rich environments, where sediments gradually cover an animal’s remains. 



However, the vulture’s feathers survived in volcanic ash - a setting not previously recognized for preserving such delicate structures.



This raises new questions about the role of volcanic environments in <a href="https://www.earth.com/news/fossil-discovery-anadoluvius-turkae-suggests-humans-originated-in-europe-not-africa/" target="_blank" rel="noreferrer noopener">fossil</a> preservation.



<h2 class="wp-block-heading" id="h-role-of-zeolite-in-preservation">Role of zeolite in preservation</h2>



By analyzing tiny samples of the fossil feathers using electron microscopes and chemical tests, the researchers uncovered an unexpected preservation mechanism. 



The feathers were found to be encased in zeolite, a mineral composed of silicon and aluminum.



“Zeolites are minerals rich in silicon and aluminum and are common in volcanic and hydrothermal geological settings," Dr. Rossi explained.



"They can form as primary minerals (with pretty crystals) or can form secondarily, during the natural alteration of volcanic glass and ash, giving the rock a ‘mudrock-like’ aspect."



The team determined that water flowing through the ash layers triggered chemical changes that led to the formation of zeolite nanocrystals. These crystals replicated the feathers’ microscopic details, thus preserving them at a cellular level.



This process had never been reported before in soft tissue fossilization, making the vulture fossil a groundbreaking discovery.



<h2 class="wp-block-heading" id="h-preserved-soft-tissues-in-a-vulture-fossil">Preserved soft tissues in a vulture fossil</h2>



Volcanic activity is usually associated with destruction, not <a href="https://www.earth.com/news/where-did-dinosaurs-come-from-missing-fossils-hold-the-secret/" target="_blank" rel="noreferrer noopener">preservation</a>. Pyroclastic flows, known for their extreme heat and rapid movement, often obliterate organic material. 



Yet, this study demonstrates that, under certain conditions, volcanic ash can encase and protect soft tissues.



“We are used to thinking that volcanic deposits are associated with hot, fast-moving pyroclastic currents that will destroy soft tissues," noted Professor Dawid A. Iurino from the University of Milan.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/03/vulture-fossil-feather_volcanic-rock_illustration_credit-Dawid-Iurino_1big.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/03/vulture-fossil-feather_volcanic-rock_illustration_credit-Dawid-Iurino_1s.webp" alt="'The Doom of the Alban Hills' a digital painting representing a possible scenario of the moments before the vulture carcass was entombed in the pyroclastic current. Credit: Dawid A. Iurino" class="wp-image-1963158"/></a><figcaption class="wp-element-caption">'The Doom of the Alban Hills' a digital painting representing a possible scenario of the moments before the vulture carcass was entombed in the pyroclastic current. Credit: Dawid A. Iurino</figcaption></figure>



"However, these geological settings are complex and can include low temperature deposits that can preserve soft tissues at the cellular level.” 



This discovery challenges the assumption that volcanic environments are unsuitable for preserving fossils. 



It suggests that low-temperature ash deposits can serve as protective enclosures for biological remains, and that this may allow scientists to study ancient creatures in ways never before possible.



<h2 class="wp-block-heading" id="h-expanding-the-search-for-fossils">Expanding the search for fossils </h2>



The findings have significant implications for paleontology. Scientists have long focused on sedimentary rocks when searching for well-preserved fossils, and may have overlooked volcanic deposits. This research suggests that volcanic rock may hold a hidden wealth of fossils with preserved soft tissues.



“The fossil record is continually surprising us, be it new fossil species, strange new body shapes, or in this case, new styles of fossil preservation. We never expected to find delicate tissues such as feathers preserved in a volcanic rock," stated Professor Maria McNamara from University College Cork.



"Discoveries such as these broaden the range of potential rock types where we can find fossils, even those preserving fragile soft tissues."



This revelation encourages researchers to revisit volcanic fossil sites with fresh eyes. It also raises the possibility that more fossils with soft tissue preservation are waiting to be uncovered in ash-rich environments.



<h2 class="wp-block-heading" id="h-a-new-chapter-in-paleontology">A new chapter in paleontology</h2>



Scientific discoveries constantly reshape our understanding of the past. 



The vulture fossil provides a glimpse into an ancient world and introduces a previously unknown pathway of fossilization. 



Its preservation within volcanic rock suggests that nature’s processes are sometimes more complex than previously thought.



As researchers continue to explore this phenomenon, future studies may uncover additional cases of soft tissue preservation in volcanic deposits. 



This could revolutionize the study of fossils and expand the possibilities for finding well-preserved specimens in unexpected places.



The study is published in the journal <a href="https://pubs.geoscienceworld.org/gsa/geology/article-abstract/doi/10.1130/G52971.1/653118/Fossil-feathers-from-the-Colli-Albani-volcanic?redirectedFrom=fulltext" target="_blank" rel="noreferrer noopener">Geology</a>.



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Vulture fossil reveals that volcanic rock can preserve feathers

The past is full of hidden secrets, and fossils offer...

Many spiders of the species Tegenaria pagana live in caves with limited vision, while others inhabit brighter areas.



This variation has drawn scientists to examine how genes guide the development of vision in Tegenaria pagana, including Dr. Efrat Gavish-Regev of The National Natural History Collections at <a href="https://www.studyinjerusalem.com/?utm_source=google&amp;utm_medium=cpc&amp;utm_campaign=US+ALO+Google+Search&amp;utm_content=Brand&amp;gad_source=1&amp;gclid=Cj0KCQjw4v6-BhDuARIsALprm330hDnhqhFoZdY_lS4PrH3Yg7CCnccG1xA3LYYjkgHiQcLx06llPK0aAtQ3EALw_wcB" target="_blank" rel="noreferrer noopener">The Hebrew University of Jerusalem</a>.



<h2 class="wp-block-heading" id="h-how-cave-life-affects-spider-vision">How cave life affects spider vision</h2>



Organisms in dark environments often lose some or all of their eyesight. Some, like blind fish or amphibians, compensate with heightened senses, a theme that also surfaces among <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC2570642/" target="_blank" rel="noreferrer noopener">subterranean spiders</a>.



Scientists are intrigued by <a href="https://www.inaturalist.org/taxa/264001-Tegenaria-pagana" target="_blank" rel="noreferrer noopener">Tegenaria pagana</a> because different populations display varying degrees of eye size. This makes it a helpful model for those who want to uncover the gene interactions that prompt vision changes.



<h2 class="wp-block-heading" id="h-gene-expression-and-eye-formation">Gene expression and eye formation </h2>



Eye development follows a genetic blueprint known as the <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC5830122/" target="_blank" rel="noreferrer noopener">retinal determination network</a>. In arthropods, this set of genes can activate when cells are instructed to form visual structures.



By comparing Tegenaria pagana with more typical spiders, researchers learn how shifts in gene expression affect eye formation. One crucial discovery is the <a href="https://www.sdbonline.org/sites/fly/neural/sineocul.htm" target="_blank" rel="noreferrer noopener">sine oculis gene</a>, which they say remains vital for <a href="https://www.earth.com/news/sydney-funnel-web-new-giant-species-of-worlds-most-dangerous-spider-identified/" target="_blank" rel="noreferrer noopener">spider</a> eyesight.



The <a href="https://link.springer.com/article/10.1186/s13227-025-00238-6" target="_blank" rel="noreferrer noopener">team</a> used fluorescence staining and confocal microscopy to track growth from fertilization to hatching. They noticed that even minor changes in embryonic timing can shift how eyes and other organs develop.



Different <a href="https://www.earth.com/news/save-a-spider-day-protecting-our-connection-with-nature/" target="_blank" rel="noreferrer noopener">spider</a> species sometimes form their body segments at varying speeds. The researchers saw that Tegenaria pagana embryos progress in unique ways, suggesting evolution can tweak shared patterns.



<h2 class="wp-block-heading" id="h-cave-species-reveal-shifts-in-vision">Cave species reveal shifts in vision</h2>



Studies on cave spiders add fresh insights to our understanding of underground habitats. Predators like Tegenaria pagana can reveal how animals cope with darkness and scarce food resources.



Some relatives of Tegenaria pagana show partial or total eye reduction, creating a range of vision abilities within the same genus. 



Researchers suggest that comparing these differences could clarify the step-by-step process that leads to eye loss.



<h2 class="wp-block-heading" id="h-how-spiders-trade-vision-for-senses">How spiders trade vision for senses</h2>



One focus of this <a href="https://link.springer.com/article/10.1186/s13227-025-00238-6" target="_blank" rel="noreferrer noopener">study</a> involved scanning a suite of genes for signs of activity in forming eyes. Each gene has a job, and if one is missing, the spider’s vision may never fully develop.



Scientists note that several <a href="https://www.earth.com/news/rethinking-arachnid-evolution-the-surprising-history-of-spiders/" target="_blank" rel="noreferrer noopener">genes</a> contribute to shaping optical tissues. This offers a clue to why some cave spiders can still see to some extent while others become blind.



<h2 class="wp-block-heading" id="h-adapting-to-life-in-darkness">Adapting to life in darkness</h2>



Reduced vision can open opportunities for enhanced contact-sensitive hairs, odor detection, or other senses. Many cave dwellers prove that what is lost in one sense often appears elsewhere.



Such trade-offs draw evolutionary biologists to cave systems worldwide. Tegenaria pagana adds a spider’s perspective to these discussions, highlighting how genes adapt in areas where light is absent.



“This research provides an essential reference for understanding how developmental and <a href="https://www.earth.com/news/slingshot-spiders-listen-for-the-right-moment-to-launch-their-webs/" target="_blank" rel="noreferrer noopener">genetic factors</a> influence eye formation in spiders.” said Dr. Gavish-Regev.



She emphasized that several Tegenaria species in Israel have assorted vision traits. This variety lets researchers gauge how gene interactions shift in response to environments with little to no light.



<h2 class="wp-block-heading" id="h-future-research-directions">Future research directions</h2>



The next research steps might involve tracking similar genes in spiders that have fully lost their eyes. Tests on <a href="https://www.researchgate.net/figure/List-of-troglomorphic-troglobitic-species-recorded-in-the-sampled-caves-in-the-Brazilian_tbl1_283984196" target="_blank" rel="noreferrer noopener">troglomorphic species</a> could lead to deeper insights into how certain genes shut down or reroute.



Findings from Tegenaria pagana may even relate to vision changes in <a href="https://www.researchgate.net/profile/Gregor-Aljancic-2/publication/269463496_Biology_and_functional_morphology_of_Proteus_anguinus_Amphibia_Caudata/links/548c45060cf2d1800d7dc089/Biology-and-functional-morphology-of-Proteus-anguinus-Amphibia-Caudata.pdf" target="_blank" rel="noreferrer noopener">other cave life</a>, such as crustaceans or amphibians that shed visual capacity over time.



The search for parallels across distant groups intrigues biologists who want to see if evolution follows similar scripts.



<h2 class="wp-block-heading" id="h-dramatic-shifts-in-subterranean-spiders">Dramatic shifts in subterranean spiders</h2>



Lab-raised populations of Tegenaria pagana promise a clearer picture of how vision genes behave during each developmental stage. Eggs collected at different intervals let scientists catch gene signals before any tissue forms.



Future research could test if genetic tweaks at early phases can produce permanent vision defects. If so, we might begin to link gene events to the dramatic shifts seen in subterranean spiders.



<h2 class="wp-block-heading" id="h-small-gene-changes-affect-vision">Small gene changes affect vision</h2>



Tegenaria pagana shows that minor changes in genes can have major effects on sight. These cave spiders add new angles to old questions about how organisms negotiate harsh, light-free habitats.



Experts plan to examine related species with fewer or missing eyes to see if the same genes come into play. This could clarify whether vision reduction follows similar routes in various caves.



Insights from Tegenaria pagana may guide future pest control strategies in human structures. By grasping how vision genes shift, we might refine ways to manage <a href="https://www.earth.com/news/some-spiders-outsmart-predators-imitating-mimicking-ants/" target="_blank" rel="noreferrer noopener">spiders</a> that thrive in dark corners.



Cave exploration groups can also benefit from this line of research, as understanding spider adaptations can provide insights into ecosystem health. If these spiders fail to maintain normal development, it might signal shifts in subterranean environments.



The study is published in the journal <a href="https://www.researchgate.net/profile/Gregor-Aljancic-2/publication/269463496_Biology_and_functional_morphology_of_Proteus_anguinus_Amphibia_Caudata/links/548c45060cf2d1800d7dc089/Biology-and-functional-morphology-of-Proteus-anguinus-Amphibia-Caudata.pdf" target="_blank" rel="noreferrer noopener">EvoDevo</a>.



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Spiders reveal how cave creatures lose their vision over time

Many spiders of the species Tegenaria pagana live in caves...

There’s something timeless about the way a puppy looks at you. Wide eyes, wagging tail, a little clumsy in its steps - that kind of innocence tugs at the heart. Puppies don’t ask for much, yet they give everything. They trust without question, love without conditions, and fill silence with soft breathing and happy barks. That’s why every year, on March 23, we celebrate National Puppy Day.



But while this day showers attention on wagging tails and floppy ears, it also carries a deeper purpose - one of compassion, <a href="https://www.earth.com/news/pandemic-puppy-owners-report-challenges-but-remain-committed/" target="_blank" rel="noreferrer noopener">awareness</a>, and responsibility.



<h2 class="wp-block-heading" id="h-purpose-of-national-puppy-day">Purpose of National Puppy Day</h2>



1National Puppy Day began in 2006, thanks to <a href="https://www.colleenpaige.com" target="_blank" rel="noreferrer noopener">Colleen Paige</a>, an animal behaviorist and author. Her goal wasn’t just to fill the world with cute puppy pictures. She established this day to spotlight the rising concerns around puppy mills and animal homelessness.



With millions of puppies born into poor conditions every year, the world needed a day that reminded people to adopt, not shop.



Colleen Paige wanted the public to understand that many dogs in shelters wait for homes while puppies are bred for profit in overcrowded and inhumane facilities. Puppy mills often keep mother dogs in cages with barely enough space to turn around. 



These mothers are bred repeatedly until they are too old or sick, at which point they are discarded. Puppies from these mills often suffer from health problems due to poor breeding practices and lack of medical care.



National Puppy Day isn't just a feel-good moment. It’s a social movement wrapped in soft fur and bright eyes. By choosing to adopt from shelters instead of buying from pet stores or online breeders, people can disrupt this cycle of cruelty. 



Paige’s initiative has since gained worldwide recognition, sparking conversations about animal rights and <a href="https://www.earth.com/news/many-people-experience-puppy-blues-with-a-new-pet/" target="_blank" rel="noreferrer noopener">responsible pet care</a>.



<h2 class="wp-block-heading" id="h-the-puppy-mill-problem">The puppy mill problem</h2>



Puppy mills are not rare. In the United States alone, there are an estimated 10,000 of these commercial breeding facilities. These mills collectively produce over 2 million <a href="https://www.earth.com/news/petting-a-dog-might-be-the-easiest-way-to-reduce-stress/" target="_blank" rel="noreferrer noopener">puppies</a> each year, many of which end up in pet shops or are sold online.



Meanwhile, nearly the same number of dogs are euthanized annually in overcrowded shelters. This staggering contrast reveals a harsh truth - there is no shortage of dogs in need of homes, only a shortage of awareness.



Puppy mills focus on quantity, not quality. Dogs are often kept in wire cages without proper bedding, food, or medical care. Their emotional needs are ignored. 



Mothers give birth repeatedly without rest, their bodies weakening over time. Puppies raised in these conditions may look healthy but often carry long-term health and behavioral issues.



By adopting, potential pet owners help break the cycle. Adoption gives homeless dogs a second chance and reduces the demand for mass breeding. National Puppy Day calls on people to educate themselves, their families, and their communities about the potentially cruel conditions in which many puppies are bred.



Change begins with knowing the truth, and this day is about more than just cuddles - it’s about making informed, <a href="https://www.earth.com/news/dogs-suffer-from-the-january-blues-just-like-humans/" target="_blank" rel="noreferrer noopener">compassionate choices</a>.



<h2 class="wp-block-heading" id="h-make-national-puppy-day-count">Make National Puppy Day count</h2>



March 23 should be more than just a day to post photos. It should be a moment of reflection, kindness, and action. People can celebrate by visiting local shelters, spending time with the animals, and learning more about how they can help. 



Shelters often use this day to host special events, encouraging community members to meet adoptable puppies and learn about rescue work.



Even if adopting isn’t an option right now, there are other ways to support the cause. Volunteering time, donating supplies, or simply sharing information online can help shelters find loving homes for their animals. 



Raising awareness within your own network can lead to more adoptions, better understanding, and stronger support systems for animals in need.



For those with pets already, National Puppy Day is a lovely excuse to give them extra attention. A longer walk, a new toy, or a few more minutes of playtime can mean the world to a <a href="https://www.earth.com/news/how-dogs-feel-smells-may-help-keep-us-safe/" target="_blank" rel="noreferrer noopener">puppy</a>. These small moments remind us why dogs are considered to be man’s best friend.



They bring loyalty, joy, and a kind of companionship that’s hard to find elsewhere.



<h2 class="wp-block-heading" id="h-puppy-facts-that-brighten-the-day">Puppy facts that brighten the day</h2>



Puppies may be young, but they have fascinating quirks that make them even more lovable. Most puppies sleep between 15 and 20 hours a day. This sleep fuels their rapid growth and development.



Dalmatians, known for their spots, are actually born without any. Their signature markings develop as they grow older. In rare cases, light-haired puppies are born with a green tint from a pigment in the womb - a color that fades within a few days.



The smallest adult dog ever recorded was just 3.8 inches (9.6 centimeters) tall. On the other end of the scale is the famous floral sculpture in Bilbao, Spain - a forty-foot-tall (12 meter) puppy covered in tens of thousands of fresh flowers.



<h2 class="wp-block-heading" id="h-a-day-to-celebrate-and-reflect">A day to celebrate and reflect</h2>



National Puppy Day 2025 is more than a celebration of cuteness. It’s a reminder that love comes with responsibility. 



Puppies are not toys. They are living beings who need time, patience, and care. Dogs deserve safe homes, not cages. They deserve kindness, not neglect.



Whether you have a dog, want one, or just love seeing them in your feed, March 23 is a day to pause and consider how we treat animals in general, and how we can do better.



So this year, take a moment to celebrate the joy of puppies. But also take a step toward change. Visit a shelter. Share a story. Adopt if you’re ready. Speak up when you see cruelty. Because behind every happy bark is a chance to build a more compassionate world. 



And every puppy, no matter where it starts, deserves that chance.



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National Puppy Day 2025: Where happiness meets responsibility

There’s something timeless about the way a puppy looks at...

Feathers did not arrive in nature as fully formed tools for flight. Their development began long before birds took to the sky. The fossil record tells a story that stretches back over 200 million years.



Now, with the help of genetic tools and carefully timed experiments, scientists can reawaken ancient traits inside of modern embryos.



This is not just about feathers. It's about how complexity arises, how it endures, and how biology protects the structures it builds. By reversing certain steps in feather <a href="https://www.earth.com/news/from-dinosaurs-to-birds-the-mysterious-origin-of-feathers/" target="_blank" rel="noreferrer noopener">development</a>, researchers reveal a hidden resilience. 



<h2 class="wp-block-heading" id="h-feather-development-before-birds">Feather development before birds</h2>



The earliest feathers didn’t help animals fly. Instead, they started as simple, hollow filaments. These "proto-feathers" likely emerged in some dinosaurs during the Triassic period, around 200 million years ago. 



There’s even evidence they may have evolved earlier, in a common ancestor of dinosaurs and pterosaurs nearly 240 million years ago.



Unlike modern feathers, proto-feathers had no central shaft, no branching barbs, and no follicle. But they still served a purpose. They helped with insulation and may have acted as colorful or patterned signals during social interaction. 



Over time, <a href="https://www.earth.com/news/bird-evolution-timeline-pushed-back-20-million-years-by-baminornis-zhenghensis-discovery/" target="_blank" rel="noreferrer noopener">natural selection</a> shaped feathers into complex tools that now support everything from flight to waterproofing.



This progression - from basic filaments to branched, aerodynamic feathers - didn’t happen randomly. It followed a path written in genes, using signaling pathways shared across the animal kingdom.



<h2 class="wp-block-heading" id="h-clues-hidden-in-bird-embryos">Clues hidden in bird embryos</h2>



Modern bird embryos offer a way to retrace this path. At the <a href="https://www.unige.ch/en/" target="_blank" rel="noreferrer noopener">University of Geneva</a>, Professor Michel Milinkovitch and his team have explored the genetics of feather formation. Their lab focuses on how molecular signals drive the development of skin structures like scales, hair, and feathers.



One such signaling system, the Sonic Hedgehog (Shh) pathway, plays a crucial role in shaping feathers. In earlier studies, the team activated this pathway in chicken embryos. 



The result was remarkable - scales on the feet of the birds transformed into permanent feathers. That experiment proved how a single shift in signaling can alter skin identity.



But what would happen if the Shh pathway were blocked instead?



"Feathers, ancient and intricate, still hold secrets that science is just beginning to unlock," noted Rory Cooper, lead author of the study.



<h2 class="wp-block-heading" id="h-ancient-feather-development-recreated">Ancient feather development recreated</h2>



To investigate, the researchers injected a drug called sonidegib into <a href="https://www.earth.com/news/bird-wings-inspire-improvements-in-airplane-safety/" target="_blank" rel="noreferrer noopener">chicken</a> embryos on their ninth day of development.



This drug shuts down the Shh pathway by targeting a key protein called Smoothened. The timing was crucial - day nine is when feather placodes begin to form, marking the start of feather bud development.



The results were dramatic. Feather buds failed to grow and remained short and unbranched. The typical invagination that forms a feather follicle was absent. Instead, the skin developed smooth, hollow filaments - almost identical to proto-feathers seen in fossils.



This temporary block in development held until the fourteenth day. After that, something unexpected happened. Feather growth resumed on its own. Chicks that hatched had patches of bare skin, but over the next several weeks, those areas filled in with normal feathers.



<h2 class="wp-block-heading" id="h-a-closer-look-at-how-feathers-recover">A closer look at how feathers recover</h2>



The researchers tracked development from embryo to hatchling using imaging and RNA sequencing. They confirmed that the Shh pathway was indeed suppressed. 



Key genes like Ptch1, Ptch2, and Gli1 were all turned down. These genes normally guide outgrowth, branching, and follicle formation. Blocking them prevented barbs and ridges from forming.



Microscopy revealed that in high-dose treatments, feather buds remained fused, stubby, and lacked branching. 



Follicle invagination - the folding-in of the skin to support feather roots - was completely absent. But despite all this, the system rebounded. By 49 days after hatching, the chicks showed normal feather coverage.



The only part that didn’t return to normal? The flight feathers. These specialized feathers, located on the posterior edge of the wing, failed to form correctly in high-dose embryos. 



Even weeks later, their positions were filled by smaller, contour-type <a href="https://www.earth.com/news/how-and-why-tropical-birds-are-so-strikingly-colorful-and-iridescent/" target="_blank" rel="noreferrer noopener">feathers</a>. This indicated that some aspects of feather identity are locked to narrow developmental windows.



<h2 class="wp-block-heading" id="h-timing-is-everything">Timing is everything</h2>



To verify that the observed effects were specific to Shh signaling, the team ran a second experiment. They combined the Shh-blocking drug with a Shh activator known as SAG. If feathers could be restored this way, it would confirm that both molecules act directly on the same pathway.



And they were. Chicks treated with both sonidegib and SAG developed normal feathers. Even when SAG was delivered one or two days after sonidegib, the feathers grew, branched, and invaginated as they should. 



Only late treatment - beyond day eleven - led to partial recovery. This showed that timing is everything in embryonic development.



"Our experiments show that while a transient disturbance in the development of foot scales can permanently turn them into feathers, it is much harder to permanently disrupt feather development itself," noted Michel Milinkovitch.



<h2 class="wp-block-heading" id="h-feathers-recover-scales-do-not">Feathers recover, scales do not</h2>



This recovery points to something fundamental about feathers. They grow from follicles that contain stem cells. These cells regenerate feathers cyclically throughout a bird’s life. 



In contrast, scales - like those on a bird’s foot - do not grow from follicles and cannot regenerate. That may explain why transformed foot scales remain feathers, while disrupted feathers bounce back.



Even at the gene expression level, this distinction is clear. After sonidegib treatment, the feathers showed temporary suppression of hundreds of genes tied to structure and shape - keratin production, signaling gradients, and branching formation. 



But the spatial map of feather follicles remained intact. Once signaling returned, so did the feathers.



Flight feathers, however, rely on precise placement and signaling levels during a short developmental window. If Shh signaling is missing at that moment, the opportunity is lost. The feather becomes ordinary, not aerodynamic.



<h2 class="wp-block-heading" id="h-ancient-mechanisms-modern-precision">Ancient mechanisms, modern precision</h2>



The entire experiment rests on a principle called reaction-diffusion. It’s a model that explains how patterns like stripes, spots, and ridges form in living tissues. 



The Shh protein works as an activator, while another molecule, Bmp2, acts as its inhibitor. Together, they create a spatial map that tells cells where to grow barbs, shafts, or follicles.



By altering the Shh signal, scientists rewrote this map. The result: broad stripes of gene activity replaced the usual dotted pattern of feather placodes. This type of disruption aligns with theories on how feathers evolved from simpler, unbranched structures. 



Proto-feathers didn’t have a patterned map yet - just the beginnings of one.



<h2 class="wp-block-heading" id="h-feather-development-and-evolution">Feather development and evolution</h2>



The study does more than recreate an ancient structure. It shows that feather development is built to recover from disruption. 



This makes sense from an evolutionary point of view. Feathers are essential to survival in many bird species. Evolution may have shaped them to resist failure - much like a city has backup systems to keep it running.



And yet, these systems remain open to change. By manipulating just one pathway, scientists can trigger a full shift in identity - from scale to feather. Or they can recreate traits that vanished millions of years ago.



It’s a reminder that the genetic blueprint of life is both sturdy and flexible. The key lies not in the parts themselves, but in the timing and tuning of their signals. Feathers evolved through such changes - and continue to teach us how form and function intertwine across deep time.



The study is published in the journal <a href="https://journals.plos.org/plosbiology/article?id=10.1371/journal.pbio.3003061" target="_blank" rel="noreferrer noopener">PLOS Biology</a>.



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Chicken embryos reveal secrets of early feather development

Feathers did not arrive in nature as fully formed tools...

Young,Golden,Retriever,For,A,Walk,With,His,Owner.,Dog

Stress can be exhausting, making even simple tasks feel like a chore. College life piles on exams and assignments, leaving many people feeling overwhelmed. A new study shows that playing with a <a href="https://www.earth.com/news/rewards-of-dog-ownership-outweigh-the-challenges/" target="_blank" rel="noreferrer noopener">friendly dog</a> for just 15 minutes can lighten that emotional load.



The research was led by senior investigator Dr. Jaruwan Khonmee from <a href="https://www.cmu.ac.th/" target="_blank" rel="noreferrer noopener">Chiang Mai University</a> in Thailand and included 122 students.



<h2 class="wp-block-heading" id="h-how-dogs-bond-with-humans-the-basics">How dogs bond with humans - the basics</h2>



There’s something incredibly special about the bond between dogs and humans - it goes way beyond companionship. 



Dogs don’t just live alongside us; they tune into our moods, read our body language, and somehow just get us. 



They know when we’re happy, when we’re stressed, when we need a nudge to go outside or a quiet moment to breathe. And we respond in kind. 



We learn to understand their barks, their tail wags, their little quirks. It’s not just loyalty - it’s this deep, wordless connection built on trust, time, and a whole lot of shared experiences.



<h2 class="wp-block-heading" id="h-dogs-help-lower-stress">Dogs help lower stress</h2>



<a href="https://archive.org/details/psychologicalstr0000laza" target="_blank" rel="noreferrer noopener">Stress</a> is a feeling of mental tension triggered by tough situations, and it can drain your energy before you realize it. Over time, stress can harm your mood, focus, and physical health in multiple ways.



College students often juggle challenging courses, part-time work, and new social circles. When responsibilities pile up, anxiety can creep in and catch people off guard.



<a href="https://pubmed.ncbi.nlm.nih.gov/2485862/" target="_blank" rel="noreferrer noopener">Cortisol</a> is a hormone that climbs when you’re tense and goes down when you’re relaxed. Lowering it can support better heart function and clearer thinking under pressure.



That’s where a quick session of <a href="https://www.earth.com/news/dog-breed-does-not-define-performance-and-ability/" target="_blank" rel="noreferrer noopener">canine interaction</a> steps in to break the cycle. A wagging tail or a nudge from a friendly snout can act like a natural mood lifter.



<h2 class="wp-block-heading" id="h-how-dogs-helped-students">How dogs helped students</h2>



In this project, students had their heart rates, saliva samples, and stress surveys measured before and after interacting with dogs. 



The researchers observed significant drops in both physical and emotional stress markers once the session ended.



Compared to just moments earlier, students’ self-reported <a href="https://www.earth.com/news/dogs-suffer-from-the-january-blues-just-like-humans/" target="_blank" rel="noreferrer noopener">stress levels</a> decreased by 33.5% after hanging out with the pup. This quick drop demonstrates how a little interaction can go a long way.



Some participants chose to cuddle or chat with the dog, while others offered treats or toys. Even short bursts of play were enough to see a noticeable shift.



<h2 class="wp-block-heading" id="h-dogs-reduce-stress-levels">Dogs reduce stress levels</h2>



“Even brief interactions with dogs can significantly reduce stress levels among university undergraduate students,” concluded the researchers. 



They noted that stress hormones in the dogs themselves appeared to drop over time, suggesting shared benefits.



Fecal tests indicated that <a href="https://www.earth.com/news/humans-and-dogs-share-genes-linked-to-obesity/" target="_blank" rel="noreferrer noopener">pups</a> had lower cortisol a week after these sessions. This finding points to the possibility that dogs might also feel relaxed when spending time with attentive humans.



Crucially, none of the six dogs used were certified therapy animals. Their friendly nature alone seemed enough to help students.



<h2 class="wp-block-heading" id="h-stress-relief-through-genuine-connection">Stress relief through genuine connection </h2>



Researchers have spent years examining the human-animal bond. One <a href="https://www.tandfonline.com/doi/abs/10.2752/089279314X14072268687808" target="_blank" rel="noreferrer noopener">project</a> found that petting a calm dog cannot only slow heart rate but also quiet the mind.



A good-natured pup provides social interaction without the same judgment people fear in formal therapy settings. Students can feel understood without having to explain every feeling or worry.



These canine sessions may work in part because they tap into <a href="https://www.health.harvard.edu/blog/co-regulation-helping-children-and-teens-navigate-big-emotions-202404033030" target="_blank" rel="noreferrer noopener">emotional co-regulation</a>, where two living beings calm each other. It’s less about a clinical approach and more about genuine connection.



That sense of warmth can reassure students who hesitate to seek human counseling. A dog’s presence often feels comforting, making it easier to let go of anxious thoughts.



<h2 class="wp-block-heading" id="h-encouraging-outcomes-for-students">Encouraging outcomes for students</h2>



Not every campus has the resources to bring in certified therapy animals. This study shows that friendly, well-behaved pets might offer help even if they lack formal training.



Some universities have started hosting dog visits during final exams to give frazzled students a break. In many cases, just a few minutes can revive a tired mind.



Researchers stress the importance of ensuring dogs enjoy the interaction. Signs of anxiety or discomfort in pets could prevent the positive effects.



Preparing a calm environment, offering treats, and supervising the sessions can keep everyone happy. It’s a balancing act that respects both human and canine comfort.



<h2 class="wp-block-heading" id="h-managing-stress-with-dog-visits">Managing stress with dog visits</h2>



Experts want to know if repeated dog sessions can bring lasting improvements. Longer studies might track stress relief over entire semesters to see if the benefits accumulate.



Some researchers wonder if these visits spark additional gains, like boosted motivation or a steadier mindset. Others are curious whether multiple short sessions are better than one extended visit. 



Further studies are needed to determine the ideal balance for ongoing stress management.



College life is not about to slow down, but dog visits seem promising for easing at least some of the mental load. Quick, simple sessions can offer a breather when books and deadlines pile high.



These findings encourage schools and organizations to consider how a wagging tail might bring calm to busy people. 



The study is published in the journal <a href="https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0318777" target="_blank" rel="noreferrer noopener">PLOS ONE</a>.



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Petting a dog is the easiest way to reduce stress without medication

Stress can be exhausting, making even simple tasks feel like...

Not all great hammerhead sharks are long-distance travelers. In fact, some prefer to stick close to home. 



Recent research focusing on sharks near Andros Island in the Bahamas has revealed that while some great hammerheads are known to migrate vast distances, others appear to settle down, likely because the local environment already meets their needs. 



This discovery could help improve conservation efforts for this critically <a href="https://www.earth.com/news/endangered-sharks-study-reveals-hidden-crisis-of-overfishing/" target="_blank" rel="noreferrer noopener">endangered</a> species.



The study was led by Tristan Lee Guttridge, director of <a href="https://www.savingtheblue.org/?srsltid=AfmBOopD-gfmsVvvpjjjgw_pZcwXw0DuEAkFdxsThf_tvfMhnr_N9qE-" target="_blank" rel="noreferrer noopener">Saving the Blue</a>, in collaboration with researchers supported by Discovery’s Shark Week.



The team focused their efforts on the Bahamas, especially around Andros Island, an area largely unexplored in terms of great hammerhead activity.



<h2 class="wp-block-heading" id="h-shark-tracking-in-the-bahamas">Shark tracking in the Bahamas </h2>



“When we started this study there was little to no information about great <a href="https://www.earth.com/news/discovery-hammerhead-sharks-hold-their-breath-to-stay-warm/" target="_blank" rel="noreferrer noopener">hammerheads</a> in the central Bahamas and no information about their habitat use at Andros, which has one of the largest fringing reefs in the world and arguably has the most pristine flats habitats in the wider Caribbean,” explained Guttridge. “We had no answers to simple questions like, what do these sharks eat?”



Until now, most shark tracking in the Bahamas focused on areas like Bimini, known for its seasonal shark visitors. However, the role of Andros Island in the sharks' life cycle remained a mystery. 



Scientists wanted to find out if the island served as a year-round habitat, a feeding ground, or even a potential mating site.



<h2 class="wp-block-heading" id="h-tagging-tracking-and-shark-science">Tagging, tracking, and shark science</h2>



Between March 2020 and June 2024, the team captured 22 great hammerhead sharks in locations that matched their known <a href="https://www.earth.com/news/top-marine-predators-may-suffer-massive-habitat-loss-by-2100/" target="_blank" rel="noreferrer noopener">habitat</a> preferences.



Using baited block rigs, they carefully caught the sharks, assessed their health, and recorded key data like sex and size. 



Muscle biopsies were taken for isotope analysis, and seven sharks were equipped with satellite trackers. Because great hammerheads are sensitive to stress, only the healthiest individuals were tagged.



The researchers didn’t rely on their captures alone. They also included opportunistic sightings, compiling a total of 78 shark encounters between 2018 and 2024. Most of these were large juveniles or adults.



Sightings spiked in January through March, with a second increase in June and July. Two of these sightings suggested recent mating, pointing to the island’s importance as a possible breeding ground.



Some sharks were even recaptured in the exact same areas years later, showing a surprising degree of site fidelity.



<h2 class="wp-block-heading" id="h-a-shark-s-preferred-neighborhood">A shark’s preferred neighborhood</h2>



The sharks didn’t use the island randomly. They favored eastern waters just off the northern and central coast of Andros, consistently returning to a relatively small 400-square-kilometer area. 



Other popular spots included edge habitats near steep reef drop-offs, where prey was abundant.



But if the sharks ventured too far south or past the northern tip of the island, they were more likely to keep moving. 



Those that left the Bahamas often traveled to the eastern United States, indicating a possible connection to the broader western Atlantic hammerhead population.



<h2 class="wp-block-heading" id="h-eating-habits-of-hammerhead-sharks">Eating habits of hammerhead sharks </h2>



Isotope analysis from the biopsies shed light on the sharks' eating habits. Barracudas and <a href="https://www.earth.com/news/climate-change-may-cause-stingrays-to-move-toward-danger/" target="_blank" rel="noreferrer noopener">stingrays</a> made up about two-thirds of the diet, with smaller sharks filling in the rest. 



However, dietary preferences varied between individuals. One shark, for instance, had a diet consisting almost entirely of silky sharks.



“Resource availability is a key driver of space use, but why don’t all of them stay if food is so abundant? We found evidence of individual variation in their diets, so deciding whether to stay or go might depend on what they feed on," said Guttridge.



“For other species, why or if migration has been linked to environmental conditions, body size, food availability, competition, and predation."



“Perhaps, like <a href="https://www.earth.com/news/young-salmon-outsmart-predators-on-their-journey-to-the-sea/" target="_blank" rel="noreferrer noopener">salmon</a>, there is a genetic component to it? We need to explore this phenomenon further.”



<h2 class="wp-block-heading" id="h-movement-patterns-of-hammerhead-sharks">Movement patterns of hammerhead sharks</h2>



Guttridge noted that the global population of great hammerheads is thought to have reduced by more than 80% over the last three generations, and genomic analysis revealed low genetic variation and inbreeding.



“Understanding the movement patterns of great hammerheads is important for improving conservation efforts. We find that some great hammerheads show residency in the Bahamas, protecting them year-round from fishing pressures.”



The Bahamas shark sanctuary offers protection to sharks that stay within its borders, but not all sharks remain in these waters. That means local conservation efforts alone aren't enough to protect the species.



“Our research showcases the importance of Bahamian waters and their protective measures. It also shows that although some individuals reside year-round in protected waters, others do not, emphasizing the need for international collaboration on conservation efforts for these mobile species," said Guttridge.



"A key next step is seeing how these hammerheads fit in with the broader north-west Atlantic population.”



Understanding who stays and who goes - and why - may be the key to keeping the species alive.



The full study was published in the journal <a href="https://www.frontiersin.org/journals/marine-science/articles/10.3389/fmars.2025.1544482/full" target="_blank" rel="noreferrer noopener">Frontiers in Marine Science</a>.



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Why some great hammerhead sharks rarely leave home

Not all great hammerhead sharks are long-distance travelers. In fact,...

Many people assume that cats are aloof and uncooperative. The results of a new study are challenging this assumption, suggesting that certain felines might be surprisingly effective in therapy and other animal-assisted services (<a href="https://aas-int.org/" target="_blank" rel="noreferrer noopener">AAS</a>).



Professor Patricia Pendry of <a href="https://wsu.edu/" target="_blank" rel="noreferrer noopener">Washington State University</a> collaborated with Belgian researchers to investigate whether some cats show consistent, friendly behavior in settings that help people cope with <a href="https://www.earth.com/news/stopping-alzheimers-before-it-starts-early-treatment-shows-potential/" target="_blank" rel="noreferrer noopener">stress</a> and anxiety.



The study was focused on how cat personality traits might fit into therapy programs, even though dogs have historically dominated this field.



<h2 class="wp-block-heading" id="h-potential-of-using-cats-in-therapy">Potential of using cats in therapy</h2>



Cat-based support programs have lagged in popularity in the United States. In some parts of Europe, however, professional teams have quietly introduced cats into schools, hospitals, and community centers, with positive anecdotal feedback.



<a href="https://pubmed.ncbi.nlm.nih.gov/22194067/" target="_blank" rel="noreferrer noopener">Researchers</a> have been digging into cat behavior for years to understand how these animals communicate with people. 



Cats form strong emotional bonds and may <a href="https://www.earth.com/news/new-therapy-for-childhood-brain-cancer-halts-tumor-formation/" target="_blank" rel="noreferrer noopener">sense</a> when someone is upset, giving them a unique way to offer comfort that differs from dogs.



<h2 class="wp-block-heading" id="h-unique-traits-that-soothe">Unique traits that soothe</h2>



Some therapy professionals report that cats can help clients feel less tense in stressful environments. These observations align with general <a href="https://pubmed.ncbi.nlm.nih.gov/24565951/" target="_blank" rel="noreferrer noopener">findings</a> that time spent with animals can lower heart rate and calm the nervous system.



Cats involved in certain AAS scenarios often display a gentle demeanor, especially when people are seated or in lower-energy <a href="https://www.earth.com/news/psilocybin-therapy-offers-hope-for-millions-with-depression/" target="_blank" rel="noreferrer noopener">moods</a>. 



Unlike many dogs, which may leap around or bark loudly, a calm cat can bring a sense of stillness that some individuals prefer.



<h2 class="wp-block-heading" id="h-screening-cats-for-therapy">Screening cats for therapy</h2>



“There’s this perception that cats just aren’t suitable for this kind of work, but our study shows that some cats may thrive in these settings,” said Pendry. 



Preliminary survey results from hundreds of Belgian cat owners revealed that specific felines show high sociability, enjoy contact with new people, and display patience when handled.



This openness may make a select group of cats better suited for therapy visits, especially when multiple clients move through a room each day. Not every cat wants this much <a href="https://www.earth.com/news/gut-health-may-be-the-key-to-anxiety-relief/" target="_blank" rel="noreferrer noopener">social interaction</a>, so experts emphasize the importance of screening and ongoing monitoring.



<h2 class="wp-block-heading" id="h-relieving-feelings-of-isolation">Relieving feelings of isolation </h2>



Therapy animals have been popular at universities, where students grapple with academic pressure and homesickness. While dogs still appear most often in the U.S., a few schools in Europe have experimented with cats to provide quieter, more low-key sessions.



Institutions that tested cat therapy sessions reported enthusiastic responses from students who already favored felines at home. Practitioners say a purring cat in someone’s lap can help relieve feelings of isolation, particularly if that person is more introverted.



<h2 class="wp-block-heading" id="h-welfare-of-therapy-cats">Welfare of therapy cats </h2>



<a href="https://www.mdpi.com/2076-2615/15/1/33">Studies</a> show that cats suitable for therapy may be tolerant of being picked up and transported. Researchers also note that some outgoing cats seem to handle bustling therapy spaces without hiding under tables or hissing.



This calm acceptance of new situations goes hand in hand with the animal’s own comfort level. Professionals warn that if a cat consistently appears tense, it’s better to remove them from the program for the sake of their well-being.



Even the best-suited cats can feel overwhelmed by long therapy <a href="https://www.earth.com/news/music-therapy-reduces-distress-in-people-with-dementia/" target="_blank" rel="noreferrer noopener">sessions</a> or large groups of people. More investigations are needed to explore the stress levels cats may experience during repeated interactions in different locations.



Caregivers and therapists often watch for signs of burnout in cats, such as excessive grooming or agitation. These signals can indicate that a break or a reduced workload is necessary, ensuring the cat remains comfortable.



<h2 class="wp-block-heading" id="h-not-all-felines-are-a-match">Not all felines are a match</h2>



Some cats are extremely social, while others are content to lounge alone at home. Advocates of cat therapy stress that the idea is not to force a reluctant cat into these roles but to let the more confident ones shine.



“It’s about recognizing that some cats may genuinely enjoy this kind of interaction,” said Pendry. She pointed out that certain outgoing felines have much in common with therapy dogs.



Professional trainers rarely work with cats in the same structured way they do with dogs. Many cats in AAS programs appear to bring their natural style of greeting, which may be enough when the cat is friendly and calm.



However, some experts think basic training could reduce fear and help cats become comfortable with unusual sounds or sudden movements. Simple exercises involving handling and social exposure might give prospective therapy cats a smoother transition into these roles.



<h2 class="wp-block-heading" id="h-the-appeal-of-quiet-companions">The appeal of quiet companions</h2>



Even in noisy environments like hospitals, a well-chosen cat can soothe patients who feel intimidated by hyperactive animals. This option might also support individuals who have had negative experiences with dogs and prefer a less boisterous companion.



Several cat breeds like <a href="https://cfa.org/breed/maine-coon-cat/" target="_blank" rel="noreferrer noopener">Maine Coons</a> and <a href="https://www.purina.co.uk/find-a-pet/cat-breeds/ragdoll" target="_blank" rel="noreferrer noopener">Ragdolls</a> are sometimes described as more tolerant of human contact, though the <a href="https://www.mdpi.com/2076-2615/15/1/33" target="_blank" rel="noreferrer noopener">study</a> did not focus on specific breeds. Researchers emphasize that individual personality matters more than general breed traits.



Belgian groups appear more open to cat-based therapies, while U.S. programs remain cautious. With growing evidence, some American facilities may soon broaden their horizons and incorporate felines for special sessions.



Pet welfare organizations suggest that expansions should be slow and monitored. Collecting data on cat temperament and stress responses will help refine best practices for feline involvement in therapy settings.



<h2 class="wp-block-heading" id="h-potential-growth-of-cat-therapy">Potential growth of cat therapy</h2>



Animal-assisted services can be beneficial for humans when done ethically. Cats offer a calmer approach for those who prefer their peaceful presence, which can be an ideal match in certain therapy contexts.



Nevertheless, it is vital to guard against pushing cats beyond their comfort zone. Programs that prioritize the cat’s autonomy and track their stress signals stand a better chance of a successful and humane experience.



As knowledge spreads, interested cat owners may look for ways to share their pets’ gentle nature with local organizations. Europe’s warmer reception could foreshadow gradual acceptance elsewhere, as more evidence supports feline therapy under the right conditions.



Focused research on cat well-being is a natural next step. Scientists are eager to pinpoint whether cats adapt to therapy work or whether personality traits drive success from the start.



The study is published in the journal <a href="https://www.mdpi.com/2076-2615/15/1/33" target="_blank" rel="noreferrer noopener">Animals</a>.



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Cats that like attention can soothe people during therapy

Many people assume that cats are aloof and uncooperative. The...

Many people know dogs have an amazing sense of smell. It helps them find lost hikers, sniff out contraband, and detect health issues. Their noses pick up odors we barely notice, offering an invisible map of the world around them.



Scientists have taken a closer look at this skill by scanning <a href="https://www.earth.com/news/dogs-can-smell-human-stress-and-it-makes-them-feel-gloomy/" target="_blank" rel="noreferrer noopener">canine brains</a> while they work their sniffing magic. The study was led by Professor Zeev Zalevsky from the Kofkin Faculty of Engineering at <a href="https://engineering.biu.ac.il/" target="_blank" rel="noreferrer noopener">Bar-Ilan University</a>. 



The researchers found key insights in the <a href="https://my.clevelandclinic.org/health/body/24894-amygdala" target="_blank" rel="noreferrer noopener">amygdala</a>, <a href="https://www.ncbi.nlm.nih.gov/books/NBK482171/" target="_blank" rel="noreferrer noopener">hippocampus</a>, and <a href="https://www.ncbi.nlm.nih.gov/books/NBK11158/" target="_blank" rel="noreferrer noopener">olfactory bulb</a> of four dog breeds, which shed light on how dogs separate one odor from another.



<h2 class="wp-block-heading" id="h-dogs-read-smells-with-their-brain">Dogs read smells with their brain</h2>



Dogs have a larger set of <a href="https://pmc.ncbi.nlm.nih.gov/articles/mid/NIHMS22337/" target="_blank" rel="noreferrer noopener">odor receptor genes</a> than humans, allowing them to detect scents in trace amounts. 



Their noses send signals to the olfactory bulb, where initial processing happens. Next, the signals reach deeper regions of the brain linked to memory, motivation, and emotion.



The research team used a remote optical sensor that could scan a dog’s brain activity while it took in four different smells. Experts say this approach might open the door for observing real-time <a href="https://www.earth.com/news/dogs-can-detect-scents-better-than-the-most-advanced-lab-tools/" target="_blank" rel="noreferrer noopener">canine</a> responses without bulky equipment.



<h2 class="wp-block-heading" id="h-why-the-amygdala-matters">Why the amygdala matters</h2>



“The findings show that the amygdala is crucial in the way dogs process and react to odors, with specific scents triggering distinct emotional and memory responses, and we are capable of optically detecting their brain activity in this region,” said Professor Zalevsky.&nbsp;



”This discovery could be the first step toward creating a device that enables us to better understand and interpret the unique way dogs perceive and differentiate smells.”



The amygdala is often associated with emotion and survival instincts. The researchers saw this region activate differently when the dogs sampled each odor, highlighting why some smells bring about strong behaviors.



<h2 class="wp-block-heading" id="h-tracking-the-smell-response-of-dogs">Tracking the smell response of dogs</h2>



“Our next step is to develop a portable, Wi-Fi-controlled device equipped with a mini camera and laser system, which could be mounted on a dog’s head and used to monitor its olfactory <a href="https://www.earth.com/news/trained-dogs-can-detect-bladder-cancer-in-other-dogs/" target="_blank" rel="noreferrer noopener">responses</a> in real time,” said Dr. Yafim Beiderman, an expert in Professor Zalevsky’s Optical Research Lab at Bar-Ilan University.



This technology could potentially transform how dogs are used in substance detection or medical diagnosis.



Some experts have looked at dogs for <a href="https://www.bmj.com/content/329/7468/712" target="_blank" rel="noreferrer noopener">cancer screening</a> and diabetes alerts. A deeper understanding of their scent processing could speed up these efforts, making it possible to gather data without waiting for canine training to finish.



<h2 class="wp-block-heading" id="h-scanning-from-a-distance">Scanning from a distance</h2>



Using lasers to pick up tiny vibrations on the surface of the skull may sound out of the ordinary. Yet <a href="https://www.sciencedirect.com/science/article/pii/S0263224123007145" target="_blank" rel="noreferrer noopener">studies</a> show that such non-invasive methods can sense blood flow and neural activity in humans. 



The researchers adapted that idea for dogs, focusing on specific brain zones where odor signals land.



Data from the sensor was processed by a machine-learning system, revealing that each area of the brain responded in unique ways. This led to the conclusion that the emotional center is a heavyweight in scent separation.



<h2 class="wp-block-heading" id="h-implications-for-health-and-safety">Implications for health and safety</h2>



Police often rely on K9 units to sniff out drugs and other illegal substances. A remote brain scanner might help them interpret the dog’s recognition of a target odor without confusion or guesswork. 



In medical fields, a quick read of a dog’s amygdala response may one day spot an illness before a patient notices symptoms.



Teams that conduct search-and-rescue missions also stand to gain. Any gadget that clarifies what a dog is smelling could guide them toward trapped individuals more efficiently.



<h2 class="wp-block-heading" id="h-a-shift-in-how-we-see-dogs">A shift in how we see dogs</h2>



The research emphasizes that dogs are more than <a href="https://www.earth.com/news/petting-a-dog-might-be-the-easiest-way-to-reduce-stress/" target="_blank" rel="noreferrer noopener">loyal companions</a>. Their noses have been described as sophisticated analyzers that monitor odors for emotion-based clues. 



Decoding those responses may add new dimensions to how people partner with animals in daily tasks.



A deeper look at the hippocampus in dogs may also reveal how memories of smells guide their actions. The research team noted that future studies could expand to more breeds and more scents, refining the technology along the way.



<h2 class="wp-block-heading" id="h-subtle-scent-triggers-from-a-dog-s-brain">Subtle scent triggers from a dog's brain</h2>



Some individuals rely on service dogs for anxiety or panic disorders. Interpreting real-time signals from the dog’s brain might uncover subtle scent triggers that a person hasn’t recognized. 



This concept extends to therapy animals, especially if professionals want to measure how dogs respond to stressful environments.



Researchers have found that dog noses can often detect changes in body chemistry, sometimes months or years before medical tests confirm a disease. Real-time tracking of this skill could produce a fast approach for problem detection, bridging the communication gap between species.



Scientists plan to explore broader ways to translate canine brainwaves into easy-to-read data. There might come a time when a single device reveals how dogs process everything from everyday household smells to suspicious substances. 



The study is published in the <a href="https://onlinelibrary.wiley.com/doi/10.1002/jbio.202400501" target="_blank" rel="noreferrer noopener">Journal of Biophotonics</a>.



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How dogs are able to "feel" smells may help keep us safe

Many people know dogs have an amazing sense of smell....

Imagine the world as if you are a krill in the Southern Ocean, where any moment a torpedo-shaped penguin could appear, devouring thousands of your fellow krill at lightning speed. Now, new research suggests that even the faintest hint of penguin droppings in the water is enough to prompt krill into escape behavior.



“Here we show for the first time that a small amount of penguin guano causes a sudden change in the feeding and swimming behaviors of <a href="https://www.earth.com/news/how-satellites-track-antarctic-krill-are-these-tiny-ocean-shrimp-in-danger/" target="_blank" rel="noreferrer noopener">Antarctic krill</a>,” said Nicole Hellessey, a postdoctoral researcher at the <a href="https://www.bigelow.org/" target="_blank" rel="noreferrer noopener">Bigelow Laboratory for Ocean Sciences</a> in Maine.



Antarctic krill play a vital role in the Southern Ocean. They serve as a major carbon sink and provide food for a large array of species, from penguins to whales. 



By some estimates, approximately 700 trillion adult Antarctic krill still swim these frigid waters, though their populations have drifted further south over time, likely due to climate change, diminishing sea ice, and acidifying ocean conditions.



<h2 class="wp-block-heading" id="h-linking-penguin-poop-to-krill-behavior">Linking penguin poop to krill behavior</h2>



<a href="https://www.earth.com/news/zooplankton-poop-can-be-used-to-store-carbon-in-the-deep-ocean/" target="_blank" rel="noreferrer noopener">Zooplankton</a> are highly sensitive to chemical cues - from signals guiding them to food or potential mates to indicators of pollution. Hellessey and her colleagues sought to determine whether krill also react to the scent of predators. 



Their study zeroed in on <a href="https://www.earth.com/news/adelie-penguins-use-sea-ice-to-migrate-thousands-of-miles-each-year/" target="_blank" rel="noreferrer noopener">Adélie penguins</a>, the southernmost-breeding penguin species, which depend on Antarctic krill for 99.6% of their diet. An adult Adélie can consume as much as 1.6 kilograms of krill each day, and the global Adélie population collectively devours around 1.5 million tons per year.



Researchers aboard the vessels Laurence M Gould and Nathaniel B Palmer in the Bransfield Strait in late 2022 netted live Antarctic krill, which they then placed in aquaria at Palmer Station. 



Meanwhile, bird researchers had collected 78 grams of Adélie guano from a colony on Torgersen Island off the Antarctic Peninsula near Palmer Station. “Smells like rotten shellfish. Not pleasant to handle,” said Hellessey, describing the guano.



<h2 class="wp-block-heading" id="h-abrupt-behavior-shifts-in-krill">Abrupt behavior shifts in krill</h2>



To test the krill’s reaction to the guano, the scientists ran trials using six to eight krill per five-minute session in a flume tank held at 1.5°C, with lights dimmed to simulate conditions at about 40 meters below the surface - the most productive layer in the <a href="https://www.earth.com/news/carbon-storage-mystery-emerges-in-the-southern-ocean/" target="_blank" rel="noreferrer noopener">Southern Ocean</a>. 



Water flowed through the flume at either 3 centimeters or 5.9 centimeters per second, and it contained either algae alone, penguin guano alone, or both combined. Each setup was tested four times.



The researchers used two automated cameras to record the movements of four krill during each trial, capturing precise data on each animal’s 3D position as well as speed and swimming direction.



The data revealed that in control settings, krill generally practiced “rheotaxis,” swimming straight upstream against the current. 



But in the presence of Adélie guano, their behavior shifted abruptly: they began to vary their swimming speed more, reaching between 1.2 and 1.5 times their usual pace, and they performed three times as many turns - over an angle that was on average 1.4 times greater than before.



<h2 class="wp-block-heading" id="h-krill-make-sacrifices-to-avoid-penguins">Krill make sacrifices to avoid penguins</h2>



A second experiment showed that guano in the water caused krill to reduce their algae consumption by 64%, plunging from 12.7 micrograms of carbon per hour per krill to 4.6 micrograms. 



This indicates that the frequent changes in swimming direction came at a cost, making them less efficient at feeding.



The researchers interpreted these dramatic differences in speed and direction as part of an avoidance response. 



“Such behavior to escape from nearby penguins would greatly increase the krill’s odds of survival. And these odds would increase exponentially in a swarm, if their neighbors could detect the same cues and communicate the danger to each other,” Hellessey said.



<h2 class="wp-block-heading" id="h-investigating-the-chemical-trigger">Investigating the chemical trigger</h2>



Though the team uncovered the behavioral shift, it is still unclear which specific compounds from penguin guano set off these alarms for krill.&nbsp;



“We hypothesize that Antarctic krill are avoiding the odor of ground-up krill and fish in the penguins’ guano. We thus expect krill to show similar swimming behaviors and suppressed feeding around seals, whales, and other types of krill predators in Antarctica,” Hellessey noted.



<h2 class="wp-block-heading" id="h-krill-signals-in-a-warming-ocean">Krill signals in a warming ocean</h2>



Given that these signals and their resulting behaviors occur in the often vast Southern Ocean, open-water conditions could dilute the cues and alter how krill respond. Moreover, warming oceans and acidification may alter how effectively these cues travel or how quickly the krill can respond.&nbsp;



“We don’t yet know how the ability of krill to sense these chemical cues and their escape behavior towards them might vary when diluted in open waters, or under global warming or ocean acidification conditions," said Hellessey. 



"Any changes to krill’s behavior could have major impacts on the future Southern Ocean, as Antarctic krill are a keystone species in this ecosystem."



<h2 class="wp-block-heading" id="h-predicting-broader-ecological-shifts">Predicting broader ecological shifts</h2>



Ultimately, this study adds an important layer to our knowledge of <a href="https://www.earth.com/news/danger-zones-climate-change-is-altering-predator-prey-dynamics/" target="_blank" rel="noreferrer noopener">predator-prey interactions</a> in polar waters. As climate shifts reshape the Southern Ocean, understanding how krill perceive and react to predator signals may help predict broader ecological shifts.&nbsp;



If krill alter their movements and feeding drastically, it could influence entire marine food webs and carbon cycling processes - a reminder that even simple chemical cues can produce outsized effects on oceanic ecosystems.



The study is published in the journal <a href="http://dx.doi.org/10.3389/fmars.2025.1508287" target="_blank" rel="noreferrer noopener">Frontiers in Marine Science</a>.



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Just a whiff of penguin poop can send krill into a frenzy

Imagine the world as if you are a krill in...

Human activity in the Galápagos Islands is quietly reshaping wildlife behavior. A new study published in the journal Animal Behaviour reveals that Galápagos yellow warblers (Setophaga petechia aureola) grow more aggressive in response to traffic noise. These <a href="https://www.earth.com/news/saving-americas-birds-scientists-declare-a-full-on-emergency-in-the-us/" target="_blank" rel="noreferrer noopener">birds</a>, found only on the islands, respond differently based on their proximity to roads.



​The study was led by researchers from <a href="https://www.aru.ac.uk/" target="_blank" rel="noreferrer noopener">Anglia Ruskin University</a> and the <a href="https://klf.univie.ac.at/" target="_blank" rel="noreferrer noopener">Konrad Lorenz Research Centre</a> at the University of Vienna. Using recorded bird songs and simulated traffic sounds, the team observed how warblers reacted in different territories.​



The results showed birds living near roads exhibited more aggression, while those farther away behaved more passively when exposed to the same noise.



<h2 class="wp-block-heading" id="h-growing-human-impact-on-islands">Growing human impact on islands</h2>



The Galápagos Islands lie over 500 miles off Ecuador’s coast. Once a quiet haven of biodiversity, the region now feels the strain of human presence. 



A rapid rise in population and tourism has increased the number of vehicles on roads. This shift transforms the once-isolated environment, bringing unexpected consequences for its native <a href="https://www.earth.com/news/birds-adapt-their-survival-strategies-to-climate-change/" target="_blank" rel="noreferrer noopener">wildlife</a>.



The Galápagos yellow warbler, a subspecies genetically distinct from its mainland relatives, serves as a biological indicator of this change. The researchers studied the birds on the islands of Floreana and Santa Cruz.



In both regions, vehicle noise prompted warblers to behave more aggressively, even on Floreana, where only around 10 vehicles are in use.



<h2 class="wp-block-heading" id="h-birds-change-their-songs-near-traffic">Birds change their songs near traffic</h2>



The scientists tested <a href="https://www.earth.com/news/birds-are-moving-north-and-breeding-earlier-in-a-changing-climate/" target="_blank" rel="noreferrer noopener">bird responses</a> by playing songs through a speaker, simulating a territorial intruder. Sometimes the sounds were paired with traffic noise. 



When this occurred near roads, birds became more aggressive - flying near the speaker and singing longer. In quieter areas, birds became less confrontational when noise accompanied the song.



This pattern suggests that long-term exposure matters. Warblers with more experience around noise adjusted their behavior in ways that could help maintain territorial control despite sound interference.



“Birds use song during territorial defense as an aggressive signal. However, if external noise such as traffic interferes with the signaling, effectively blocking this communication channel, increasing physical aggression would be an appropriate response,” noted Dr. Caglar Akcay, senior lecturer in behavioural ecology at Anglia Ruskin University.



The research suggests these birds are learning to adapt. Changes in song length and pitch help their calls rise above low-frequency traffic sounds. 



In all territories, birds raised the minimum frequency of their songs when traffic was present. This adjustment could improve their chances of being heard.



<h2 class="wp-block-heading" id="h-behavioral-flexibility-and-conservation">Behavioral flexibility and conservation</h2>



The findings shed light on the unexpected reach of human activity. Even in the Galápagos - long seen as a sanctuary for natural evolution - <a href="https://www.earth.com/news/birds-are-breathing-in-plastic-what-does-that-mean-for-us/" target="_blank" rel="noreferrer noopener">birds</a> now must compete with the noise of progress.



“Our results show that the change in aggressive responses in yellow warblers occurred mainly near roads. Birds occupying roadside territories on both islands, and therefore having regular experience of traffic noise, may have learned to increase physical aggression when the territorial intrusion was accompanied by traffic noise,” said Dr. Akcay.



Beyond aggression, warblers demonstrate flexibility. They tweak their songs to cut through the clamor. These subtle changes show nature’s resilience, but they also signal a need for reflection.



“Our study shows the importance of considering behavioral plasticity in conservation efforts and developing strategies to mitigate the effects of noise pollution on wildlife. It also highlights the significant impact of human activities on wildlife behavior, even in relatively remote locations such as the Galápagos Islands,” noted Dr. Akcay.



Understanding this behavioral flexibility may guide future conservation. It reminds us that protecting biodiversity requires more than preserving land - it demands attention to the noise we bring with us.



<h2 class="wp-block-heading" id="h-traffic-noise-changes-birds-behavior">Traffic noise changes birds’ behavior</h2>



This study urges conservationists and policymakers to look beyond visible damage. Roads, buildings, and pollution are easy to spot. Noise, on the other hand, slips in silently, altering <a href="https://www.earth.com/news/tropical-birds-can-handle-climate-variability/" target="_blank" rel="noreferrer noopener">ecosystems</a> in less obvious ways. 



Yet its effects are clear. For the Galápagos yellow warbler, this may mean adjusting song and behavior just to be heard and understood.



The warbler’s story is a quiet warning: the modern world reaches even the most distant corners. If we are to protect these natural wonders, we must consider not only what we build, but what we sound like as we do.



The study is published in the journal <a href="https://www.sciencedirect.com/science/article/pii/S0003347225000466" target="_blank" rel="noreferrer noopener">Animal Behaviour</a>.



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Some birds get 'road rage' when exposed to traffic noise

Human activity in the Galápagos Islands is quietly reshaping wildlife...

Modern birds are closely related to dinosaurs, as seen by comparing flightless species like chickens and ostriches, which walk on two hind legs, or predatory hawks and eagles with their keen senses and sharp talons, to small theropod dinosaurs.&nbsp;



Still, birds have diverged in crucial ways from their reptilian predecessors. One vital turning point was their development of larger brains, which spurred changes in skull size and shape.



Recent work by researchers at the <a href="https://www.uchicago.edu/en" target="_blank" rel="noreferrer noopener">University of Chicago</a> and the <a href="https://missouri.edu/" target="_blank" rel="noreferrer noopener">University of Missouri</a> demonstrates how these physical transformations affected how <a href="https://www.earth.com/news/saving-americas-birds-scientists-declare-a-full-on-emergency-in-the-us/" target="_blank" rel="noreferrer noopener">birds</a> move and utilize their beaks to eat and interact with the world - adaptations that helped them become one of the most diverse lineages on Earth.



<h2 class="wp-block-heading" id="h-complex-nature-of-a-wiggly-skull">Complex nature of a “wiggly” skull</h2>



Unlike many other animals, modern birds, along with certain snakes and fishes, have skulls whose jaws and palates are not firmly fixed in place.&nbsp;



Alec Wilken, a graduate student in integrative biology at the University of Chicago and lead author of this new study, calls this kind of flexible anatomy “wiggly.” He notes that such a trait complicates attempts to understand its function.&nbsp;



“Just because you have a joint there, that doesn’t mean that you know how it moves. So, you also have to think about how muscles are going to be pulling on the joint, what kind of torque they have, and how other joints in the head limit the mobility,” he explained.



<h2 class="wp-block-heading" id="h-investigating-how-bird-skulls-evolved">Investigating how bird skulls evolved</h2>



Wilken first became involved in this project in 2015 while studying at the University of Missouri. 



There, Casey Holliday, an associate professor of pathology and anatomical sciences, had received support from the <a href="https://www.nsf.gov/" target="_blank" rel="noreferrer noopener">National Science Foundation</a> (NSF) to investigate how bird skulls, jaw muscles, and feeding mechanics evolved from their <a href="https://www.earth.com/news/where-did-dinosaurs-come-from-missing-fossils-hold-the-secret/" target="_blank" rel="noreferrer noopener">dinosaur</a> lineage to modern birds.



Wilken contributed to the research by analyzing data from computer tomography (CT) scans of fossils and existing birds, as well as the skulls of other reptiles such as alligators. 



The gathered data then supported the creation of 3D models that track muscle positions, movements, and the physics of how they operate together.



<h2 class="wp-block-heading" id="h-advantages-of-modern-bird-skulls">Advantages of modern bird skulls</h2>



One distinctive feature of modern birds is referred to as “cranial kinesis,” which is the capacity to move different portions of the skull independently. This affords birds an evolutionary edge, letting them open or expand their palates and use their beaks in various ways.



“Having a wiggly head like this really gives them a lot of evolutionary benefits,” Wilken said. Parrots, for instance, employ their beaks to climb, while other birds break open tough seeds and nuts.&nbsp;



“In some ways, the beak functions like a surrogate hand, but being able to move the palate around while eating is also mission critical to helping them acquire food and survive.”



<h2 class="wp-block-heading" id="h-the-path-from-dinosaurs-to-birds">The path from dinosaurs to birds</h2>



From analyzing these 3D models, the scientists observed that as non-avian theropod dinosaurs developed increasingly larger brains and skulls, muscles shifted into arrangements that allowed for more mobile palates and jaws.&nbsp;



Consequently, these transformations increased muscle force and supported cranial kinesis in the majority of today’s birds.



“We see this cascade of changes that happened along the dinosaur to bird transition,” said Holliday. “A large part of it hinges upon when birds evolved a relatively large <a href="https://www.earth.com/news/bird-brain-study-will-shed-new-light-on-avian-intelligence/" target="_blank" rel="noreferrer noopener">brain</a>. Just like in humans, bigger brains drive a lot of changes in the skull.”



Over time, paleontological findings have shown that the line between dinosaurs and birds is considerably blurred, especially since many dinosaurs sported feathers and some were capable of flight.&nbsp;



However, the scientists noted that truly flexible skulls and palates appeared later than species such as Archaeopteryx, leading them to speculate that cranial kinesis may turn out to be a key factor distinguishing modern birds from more primitive dinosaur-like birds.



<h2 class="wp-block-heading" id="h-a-blueprint-for-future-understanding">A blueprint for future understanding</h2>



While it is well established that <a href="https://www.earth.com/news/study-reveals-secrets-of-the-evolution-of-prehistoric-reptiles/" target="_blank" rel="noreferrer noopener">prehistoric reptiles</a> gave rise to the birds we now see flying overhead, the genetic and mechanical steps along that journey remain a topic of intense investigation.&nbsp;



This latest research strengthens the idea that the interplay between a bigger brain and skull modifications allowed birds to free up their jaws and palates, leading to vast ecological success.



Ultimately, the improved skull flexibility and diversified feeding methods among birds mirror the complicated interplay of evolutionary pressures that have continued since the time of dinosaurs.&nbsp;



The new study represents only one step in unravelling how birds learned to harness their beaks’ capabilities, and how earlier dinosaur species formed the foundation for today’s avian biodiversity.



The study is published in the journal <a href="http://dx.doi.org/10.1073/pnas.2411138122" target="_blank" rel="noreferrer noopener">Proceedings of the National Academy of Sciences</a>.



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‘Wiggly’ skulls helped birds evolve from dinosaurs

Modern birds are closely related to dinosaurs, as seen by...

Scientists have identified a new fossil species of freshwater fish, Ferruaspis brocksi, from a site near Gulgong, in NSW, Australia.



This discovery, led by Dr. Matthew McCurry from the <a href="https://australian.museum" target="_blank" rel="noreferrer noopener">Australian Museum</a> and <a href="https://www.unsw.edu.au" target="_blank" rel="noreferrer noopener">UNSW Sydney</a>, provides a rare glimpse into Australia’s ancient aquatic life. 



The fossil, which is estimated to be 15 million years old, preserves both the fish's stomach contents and its color patterns. The Journal of Vertebrate Palaeontology has published the findings.



Ferruaspis brocksi belongs to the Osmeriformes order, which includes <a href="https://www.earth.com/news/ancient-fish-had-flexible-joints-like-humans/" target="_blank" rel="noreferrer noopener">species</a> like the Australian Grayling and Australian Smelt.



It is the first freshwater smelt fossil found in Australia. The species was named in honor of Professor Jochen J. Brocks from the <a href="https://www.anu.edu.au" target="_blank" rel="noreferrer noopener">Australian National University</a>, who contributed to fossil discoveries at McGraths Flat.



<h2 class="wp-block-heading" id="h-tracing-the-evolution-of-osmeriformes">Tracing the evolution of Osmeriformes</h2>



Dr. McCurry emphasized that before the discovery of this fossil, scientists lacked evidence to confirm when Osmeriformes first arrived in Australia.



“The discovery of the 15 million-year-old freshwater fish fossil offers us an unprecedented opportunity to understand Australia’s ancient ecosystems and the evolution of its fish species, specifically the Osmeriformes group during the Miocene epoch, 11-15 million years ago,” McCurry said.



Without fossils, researchers could not determine whether these fish had <a href="https://www.earth.com/news/tiktaalik-fossil-discovery-sheds-light-on-how-fish-walked-onto-land/" target="_blank" rel="noreferrer noopener">evolved</a> significantly over time. This new find provides crucial evidence for understanding how they adapted to ancient Australian waters.



<h2 class="wp-block-heading" id="h-what-did-the-fish-fossil-reveal">What did the fish fossil reveal?</h2>



The well-preserved fossil reveals fascinating details about the fish’s diet. The stomach contents show that it fed on various invertebrates, mainly small phantom midge larvae. 



This level of preservation is rare and helps scientists reconstruct past <a href="https://www.earth.com/news/plesiosaur-fossil-contains-soft-tissue-preserved-for-183-million-years/" target="_blank" rel="noreferrer noopener">ecosystems</a> with greater accuracy.



“One of the fossils even shows a parasite attached to the tail of the fish. It’s a juvenile freshwater mussel called a glochidium. These juvenile mussels attach themselves to the gills or tails of fish to hitch rides up and down streams,” McCurry added.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/03/fish_Ferruaspis-brocksi_fossil_stomach-contents_15-million-years-old_credit-Salthy-Dingo_1m.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/03/fish_Ferruaspis_fossil_stomach-contents_15-million-years-old_credit-Salthy-Dingo_1s.webp" alt="A 15-million-year-old fish fossil, Ferruaspis brocksi, with preserved stomach contents. Credit: Salthy Dingo" class="wp-image-1962871"/></a><figcaption class="wp-element-caption">A 15-million-year-old fish fossil, Ferruaspis brocksi, with preserved stomach contents. Credit: Salthy Dingo</figcaption></figure>



The species’ name reflects its discovery in iron-rich rock. “Ferru” comes from the Latin word “ferrum,” meaning iron, while “brocksi” honors Professor Brocks.



<h2 class="wp-block-heading" id="h-honoring-a-scientific-contribution">Honoring a scientific contribution</h2>



Professor Brocks expressed excitement about having this fossil species named after him.



“Collecting fossils at McGrath Flat is a highlight for me every year. Splitting the rust-red slabs of rock is like opening an ancient book, revealing the creatures that inhabited an Australian oxbow lake some 15 million years ago," exclaimed Professor Brocks.



"This little fish is one of the most beautiful fossils there, and finding the first vertebrate among the abundant plant and insect fossils was a real surprise. Having F. brocksi named after me is a real joy.” 



The McGraths Flat fossil site continues to provide remarkable insights into prehistoric life, and contributes to a better understanding of Australia’s ecological past.



<h2 class="wp-block-heading" id="h-revealing-the-fish-s-coloration">Revealing the fish’s coloration</h2>



Dr. Michael Frese from the <a href="https://www.canberra.edu.au" target="_blank" rel="noreferrer noopener">University of Canberra</a> and <a href="https://www.csiro.au/en/" target="_blank" rel="noreferrer noopener">CSIRO</a> highlighted another exciting aspect of the research - the ability to determine the fish’s color pattern.



“The fish was darker on its dorsal surface, lighter in color on its belly and had two lateral stripes running along its side,” Dr. Frese said.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/03/fish_Ferruaspis-brocksi_fossil_illustration_15-million-years-old_credit-Alex-Boersma_1m.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/03/fish_Ferruaspis-brocksi_fossil_illustration_15-million-years-old_credit-Alex-Boersma_1s.webp" alt="A school of Ferruaspis is chased by the extinct platypus, Obdurodon. Credit: Alex Boersma" class="wp-image-1962873"/></a><figcaption class="wp-element-caption">A school of Ferruaspis is chased by the extinct platypus, Obdurodon. Credit: Alex Boersma</figcaption></figure>



Using a powerful microscope, scientists identified melanosomes, which are tiny structures responsible for producing color. 



While melanosomes have helped reconstruct the colors of ancient feathers, this is the first time they have been used to determine the color pattern of a long-extinct fish.



<h2 class="wp-block-heading" id="h-site-of-exceptional-fossil-preservation">Site of exceptional fossil preservation</h2>



Professor Kris Helgen, Director and Chief Scientist at the Australian Museum Research Institute, praised the ongoing research at McGraths Flat.



“Dr. Matt McCurry’s work at the McGraths Flat fossil site has been outstanding. This is one of many discoveries made at this site, which continues to play a significant role in advancing our understanding of Australia’s evolution during the Miocene era.”



McGraths Flat is one of the rare fossil sites in Australia classified as a "Lagerstätte" - a site with exceptionally well-preserved fossils. 



Located in the Central Tablelands of NSW, it offers a unique window into an ancient rainforest ecosystem.



<h2 class="wp-block-heading" id="h-what-do-fish-fossils-reveal-about-ancient-australia">What do fish fossils reveal about ancient Australia?</h2>



Dr. McCurry explained that fossils from this site, dating back 11 to 16 million years, show that the region was once a temperate, wet rainforest teeming with life. 



These discoveries help scientists reconstruct ancient landscapes and understand the biodiversity of prehistoric Australia.



The initial McGraths Flat expedition in 2017 received funding from a descendant of Robert Etheridge, a renowned English palaeontologist who played a crucial role in developing the Australian Museum’s collections. 



Etheridge launched a series of scientific expeditions that continue today, ensuring that Australia’s rich fossil heritage remains a key focus for researchers.



The discovery of Ferruaspis brocksi is another milestone in understanding how <a href="https://www.earth.com/news/coelacanth-ngamugawi-wirngarri-new-species-living-fossil-fish-survived-over-400-million-years/" target="_blank" rel="noreferrer noopener">ancient species</a> thrived and adapted in Australia’s evolving landscapes.



The study is published in the <a href="https://www.tandfonline.com/doi/full/10.1080/02724634.2024.2445684" target="_blank" rel="noreferrer noopener">Journal of Vertebrate Paleontology</a>. 



Image Credit: Salthy Dingo



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Stomach contents preserved after 15 million years in fish fossil

Scientists have identified a new fossil species of freshwater fish,...

A new study has found that the H5N1 avian influenza virus is mutating to evade immune defenses in mammals following prior infection or vaccination.



The research, led by <a href="https://www.charlotte.edu/" target="_blank" rel="noreferrer noopener">UNC Charlotte</a>, emphasizes the growing threat of <a href="https://www.earth.com/news/efforts-to-control-bird-flu-are-not-working-are-humans-next/" target="_blank" rel="noreferrer noopener">H5N1</a> to both agriculture and public health.



“H5N1 can infect avian and mammalian livestock and jump to humans,” the authors wrote. highlighting that new strains appear increasingly resistant to existing antibodies. This evolution, they caution, suggests that older vaccine formulas may lose effectiveness.



“This study shows a trend of weakening binding affinity of existing antibodies against H5 isolates over time, indicating that the H5N1 virus is evolving immune escape from our therapeutic and immunological defenses,” noted the researchers.



<h2 class="wp-block-heading" id="h-rapid-shifts-in-bird-flu-virus">Rapid shifts in bird flu virus</h2>



By running large-scale computational models of specific viral proteins binding with neutralizing antibodies, the research team discovered “an overall worsening in <a href="https://www.earth.com/news/experts-have-found-powerful-antibodies-that-neutralize-all-covid-variants/" target="_blank" rel="noreferrer noopener">antibody</a> affinity to more recent H5N1 isolates.”&nbsp;



“If one makes an H5N1 vaccine with a previous vaccine candidate virus, the vaccine will have less efficacy, based on our measurements of how much the virus has evolved in recent years,” explained lead author Colby T. Ford, a visiting scholar at UNC Charlotte’s <a href="https://cipher.charlotte.edu/" target="_blank" rel="noreferrer noopener">Center for Computational Intelligence to Predict Health and Environmental Risks</a> (CIPHER).



Conducted under the guidance of assistant professor Richard Allen White III, and CIPHER co-director Daniel Janies, the UNC Charlotte team joined forces with <a href="https://web.mit.edu/" target="_blank" rel="noreferrer noopener">Massachusetts Institute of Technology</a> (MIT) researchers Rafael Jaimes III and Phillip J. Tomezsko to explore how the H5N1 virus is adapting so quickly.



<h2 class="wp-block-heading" id="h-mounting-zoonotic-risk">Mounting zoonotic risk</h2>



Analyzing 1,804 antigen-antibody interactions, the researchers examined how the virus’s hemagglutinin subunit changed from 1996 to 2018.&nbsp;



By applying high-performance computational techniques, they tracked the virus’s “antigenic drift” - small cumulative mutations that hamper the effectiveness of immune defenses from earlier infections or vaccines.



The new measurements of how much the bird flu virus has evolved in recent years confirmed that H5N1 is becoming less recognizable to established antibodies.



“These results indicate that the virus has potential to move from epidemic to pandemic status,” wrote the researchers.



<h2 class="wp-block-heading" id="h-emergence-across-multiple-species">Emergence across multiple species</h2>



Though H5N1 has primarily circulated in birds, it has jumped to <a href="https://www.earth.com/news/avian-influenza-h5n1-marine-mammals-spreading-worldwide/" target="_blank" rel="noreferrer noopener">mammals</a> and, rarely, to humans.&nbsp;



In the past year, the virus was found in dairy cattle in at least 17 U.S. states, and the <a href="https://www.cdc.gov/index.html" target="_blank" rel="noreferrer noopener">Centers for Disease Control and Prevention</a> (CDC) reported 70 human cases, including one fatality, in the United States since January 2022.&nbsp;



Worldwide, according to the <a href="https://www.who.int/" target="_blank" rel="noreferrer noopener">World Health Organization</a>, H5N1 has been linked to 466 human deaths since 2003.



Between January 2022 and March 2025, the CDC also documented 12,510 H5N1 outbreaks among wild birds within the U.S., virus detections in 51 jurisdictions and 166,417,923 affected poultry.



Such widespread, cross-species infections strongly indicate that avian influenza can be considered a pandemic among animal populations, raising fears of a future human pandemic.



<h2 class="wp-block-heading" id="h-birds-flu-vaccination-and-public-health">Birds flu vaccination and public health</h2>



In discussing how to avert the looming threat, the authors argue that a new approach to <a href="https://www.earth.com/news/universal-influenza-vaccine-could-offer-lifetime-immunity/">vaccine</a> development may be needed.&nbsp;



These findings indicate that once the bird flu virus modifies itself significantly, older vaccines will have less efficacy, making it essential to develop and regularly update H5N1 vaccines reflecting the virus’s continuous genetic changes.



Furthermore, the study’s results highlight the power of high-performance computing in mapping viral evolution. By integrating AI-based protein folding with physics-based simulations, researchers can anticipate changes in viral structure and better inform policy decisions.&nbsp;



<h2 class="wp-block-heading" id="h-bird-flu-s-potential-for-pandemic-status">Bird flu’s potential for pandemic status</h2>



With H5N1 already widespread among wild birds and expanding its foothold in mammalian hosts, the virus’s cross-species jumps present a significant concern.&nbsp;



According to the experts, more robust monitoring, updated vaccination strategies, and ongoing computational analyses will be crucial in mitigating a potential outbreak.&nbsp;



As Janies concluded, computational modeling can help experts “tune our intuition to the right approaches” for vaccine design and intervention strategies before a fast-adapting virus gains an uncontrollable edge.



The study is published in the journal <a href="https://dx.doi.org/10.1016/j.ebiom.2025.105632" target="_blank" rel="noreferrer noopener">eBioMedicine</a>.&nbsp;



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Bird flu virus is rapidly evolving to evade immune defenses

A new study has found that the H5N1 avian influenza...

Coral reefs face threats from many sources, but the crown-of-thorns starfish is often singled out for its ability to chomp through living coral at staggering rates.



<a href="https://scispace.com/pdf/the-acanthaster-phenomenon-1fnwsb66cy.pdf" target="_blank" rel="noreferrer noopener">Scientists</a> have puzzled over this starfish’s boom-and-bust population cycles, which can leave once-colorful coral communities in serious trouble.



Crown-of-thorns starfish numbers can spike quickly, damaging reefs from Australia to other parts of the Indo-Pacific. 



Previous explanations have focused on shifting ocean conditions or lack of predators, yet a recent <a href="https://www.pnas.org/doi/10.1073/pnas.2424560122" target="_blank" rel="noreferrer noopener">study</a> highlights a surprising group that appears to gobble up young starfish before they mature.



<h2 class="wp-block-heading" id="h-small-crabs-help-control-starfish-numbers">Small crabs help control starfish numbers</h2>



“Using our newly developed eDNA techniques to detect COTS, we found COTS DNA in the guts of seven species of decapod caught across more than 1,000 km of the Great Barrier Reef. Plus we found fewer crabs in areas prone to COTS outbreaks,” said study senior author Dr. Sven Uthicke from the <a href="https://www.aims.gov.au/" target="_blank" rel="noreferrer noopener">Australian Institute of Marine Science</a>. 



Some <a href="https://www.earth.com/news/breaks-in-ancient-coral-growth-reveal-earths-climate-past/" target="_blank" rel="noreferrer noopener">reefs</a> seem to carry pockets of these small <a href="https://www.britannica.com/animal/decapod" target="_blank" rel="noreferrer noopener">decapod creatures</a>, which are ten-legged crustaceans that often lurk in cracks and under rubble. 



The researchers found that their absence in certain spots matched places where starfish outbreaks flared up.



<h2 class="wp-block-heading" id="h-crabs-eat-young-starfish">Crabs eat young starfish </h2>



“Consuming <a href="https://www.gbrbiology.com/2022/05/26/juvenile-crown-of-thorns-starfish/" target="_blank" rel="noreferrer noopener">juvenile COTS</a> is a highly effective way to reduce COTS populations because, not only are they removed before they can start feeding on <a href="https://www.earth.com/news/coral-bleaching-has-reached-catastrophic-levels-on-the-great-barrier-reef/" target="_blank" rel="noreferrer noopener">coral</a>, but they can be removed in large numbers because they are so small,” said Dr. Uthicke. 



Small starfish tend to spend time hiding in rubble and among broken coral fragments. The researchers discovered that crusty guardians live in those same hiding spots, and their diets sometimes include juvenile starfish.



“It’s a numbers game. Some of the crabs can eat 20 juveniles a day, whereas fish or triton may eat one adult every few days or per week,” said Dr. Uthicke. 



Differences in how often these crabs show up across the <a href="https://www.earth.com/news/fish-diversity-has-changed-dramatically-on-the-great-barrier-reef/" target="_blank" rel="noreferrer noopener">reef</a> may explain why some sections avoid major starfish invasions.



By using <a href="https://iucn.org/resources/issues-brief/environmental-dna" target="_blank" rel="noreferrer noopener">eDNA</a> (environmental DNA) methods, scientists found proof of starfish consumption without needing direct observation. Targeting scraps of genetic material helps capture hidden feeding patterns that traditional surveys might overlook.



<h2 class="wp-block-heading" id="h-wider-reef-implications">Wider reef implications</h2>



Scientists suspect that fewer small cryptic predators could give young starfish a better chance of surviving to adulthood. Removing juveniles early on may hold the key to keeping starfish populations in check.



A single decapod crab might appear harmless, yet large groups can collectively remove countless baby starfish. This kind of steady predation could halt population spikes before they cause coral damage.



Hidden crabs bring renewed attention to natural pest control on <a href="https://www.earth.com/news/restored-coral-reefs-can-bounce-back-in-just-four-years/" target="_blank" rel="noreferrer noopener">reefs</a>. Managers usually track adult starfish as they munch their way across corals, but juveniles slip below the radar and can later emerge en masse.



Marine experts believe many reef inhabitants remain poorly understood. The study suggests these overlooked animals could influence overall coral health by feeding on starfish in ways that bigger predators might not.



<h2 class="wp-block-heading" id="h-protecting-crab-populations">Protecting crab populations </h2>



Decapod crabs rely on healthy, structurally complex habitats. When reefs degrade, key crab hideouts disappear, leading to fewer opportunities for them to find and eat juvenile starfish.



Scientists note that preserving coral rubble habitat might help maintain crab populations. Extra protective measures could make a difference, especially in places that have experienced intense fishing or widespread coral decline.



Future work may look at what drives crab populations up or down and whether certain types of rubble or coral attract more crabs. Researchers might also see if artificial reefs provide enough shelter for these decapods to flourish.



Insights like these can improve management. Rather than focusing solely on adult starfish, officials could encourage conditions where small crustaceans thrive and reduce problems before they start.



<h2 class="wp-block-heading" id="h-a-sign-of-hidden-connections">A sign of hidden connections</h2>



Crustaceans are not the only puzzling factor in starfish control, yet their impact sparks curiosity about other nooks and crannies of reef life. Everything from tiny worms to <a href="https://www.earth.com/news/great-barrier-reef-is-on-the-brink-of-extinction/" target="_blank" rel="noreferrer noopener">reef</a> bacteria may hold clues.



Each new finding reminds us that reefs are webs of interactions with many unsung heroes. Understanding these links may be essential for long-term reef survival.



Researchers suggest that bolstering small predator populations could be a smart tactic in starfish management. Keeping these animal communities strong may help reefs bounce back faster when facing constant stress.



Local conservation groups already invest in large-scale starfish culls, but it may be easier to back up that work by maintaining conditions for crabs and other protective critters. The goal is to strike a balance that curbs harmful sea star numbers without disrupting other species.



The study is published in <a href="https://www.pnas.org/doi/10.1073/pnas.2424560122" target="_blank" rel="noreferrer noopener">Proceedings of the National Academy of Sciences</a>.



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Tiny crabs protect reefs by eating baby crown-of-thorns starfish

Coral reefs face threats from many sources, but the crown-of-thorns...

Biologging sensors attached to animals help researchers collect valuable data about marine environments. This data helps monitor human activities, such as fishing, pollution, and noise disturbances from boats and construction, providing insights into their impact on marine life.



A recent study from Kobe University highlights the importance of integrating data from different sources to create an “Internet of Animals” with open-access standards.



Human activities affect marine life in multiple ways. Fishing, industrial waste, and underwater construction alter <a href="https://www.earth.com/news/world-wildlife-day-2025-a-global-call-to-protect-nature/" target="_blank" rel="noreferrer noopener">habitats</a> and disrupt ecosystems. 



“There is a wealth of oceanographic data from research vessels, drifting buoys and satellites," said Professor IWATA Takashi, an animal ecologist at <a href="https://www.kobe-u.ac.jp/en/" target="_blank" rel="noreferrer noopener">Kobe University</a>.



"But due to technological and economic constraints, there are many observation gaps and some areas are inaccessible to humans, such as under sea ice or during harsh weather.” 



Understanding how these changes impact individual animals is difficult, making it challenging to design effective conservation strategies.



<h2 class="wp-block-heading" id="h-biologging-window-into-animal-experiences">Biologging: Window into animal experiences</h2>



Attaching small sensors, cameras, or tracking devices to wild animals is known as biologging. Scientists originally used biologging to study animal behavior and movement patterns. Now, it also helps analyze environmental changes affecting <a href="https://www.earth.com/news/what-animal-will-replace-humans-as-earths-dominant-species-this-scientist-has-an-idea/" target="_blank" rel="noreferrer noopener">marine life</a>.



“We try to minimize the impact this has on the animals by keeping the overall weight of the devices to less than 3% of the animal’s body weight, or even less than 1% for larger animals, and many researchers keep developing smaller and smaller devices," explained Iwata.



This method allows researchers to gather data without disturbing natural behaviors.



Biologging follows a Lagrangian observational method, meaning it moves with the animals, offering insights that fixed observation platforms like satellites or buoys cannot provide. It records a variety of environmental parameters, including temperature, salinity, and oxygen levels.



<h2 class="wp-block-heading" id="h-advancements-in-biologging-research">Advancements in biologging research</h2>



The researchers reviewed the latest advancements in biologging. Their analysis showed that biologging has improved typhoon forecasts, revealed differences in how turtle species react to plastic waste, exposed illegal fishing, and influenced the design of bird-friendly offshore wind farms.



“This review showed that while biologging alone is insufficient, it can fill in the gaps in existing knowledge," said Iwata.



"It provides a new type of data that differs from the wide-area environmental information obtained from earth observation satellites and other sources to tackle a broad range of <a href="https://www.earth.com/news/animals-secretly-reshape-landscapes-in-powerful-ways/" target="_blank" rel="noreferrer noopener">environmental issues</a>."



Combining biologging with other research methods offers a more complete understanding of marine ecosystems.



<h2 class="wp-block-heading" id="h-tackling-ocean-warming-and-pollution">Tackling ocean warming and pollution</h2>



Biologging offers a crucial tool for tracking ocean warming. By attaching GPS loggers to seabirds and marine mammals, scientists can measure ocean currents, wind patterns, and temperature changes over time. These observations have helped improve climate models and typhoon <a href="https://www.earth.com/news/animals-change-their-daily-schedules-when-tourists-are-watching/" target="_blank" rel="noreferrer noopener">tracking</a>.



Plastic pollution remains a major concern, especially its impact on marine life. Cameras attached to sea turtles have captured floating plastic bags, providing direct evidence of pollution in marine habitats. 



Loggerhead turtles swim past plastic, while green turtles sometimes mistake it for food. Such species-specific behaviors help shape targeted conservation strategies.



Chemical pollution also threatens marine ecosystems. Persistent organic pollutants accumulate in seabirds and marine mammals, serving as bio-indicators of contamination. Tracking these animals allows scientists to monitor pollution levels across different ocean regions.



<h2 class="wp-block-heading" id="h-challenges-in-fishery-management">Challenges in fishery management</h2>



Overfishing and bycatch pose significant threats to marine biodiversity. Biologging helps identify migration routes and breeding grounds for fish species like tuna and cod. This information supports more sustainable fishing policies.



Additionally, biologging has revealed that some marine animals, such as seals and whales, actively seek out fishing vessels to feed on discarded fish. This behavior increases the risk of entanglement and vessel collisions. 



Understanding these interactions can help develop better deterrent strategies.



<h2 class="wp-block-heading" id="h-conservation-and-marine-protected-areas">Conservation and marine protected areas</h2>



Noise pollution from shipping and offshore wind farms disrupts marine animals, particularly cetaceans that rely on echolocation. 



Biologging has demonstrated that naval sonar and shipping noise affect whale behavior, influencing feeding and migration patterns. Some studies have proposed raising turbine heights to minimize risks for seabirds.



Biologging also plays a key role in marine protected area (MPA) management. Data collected from tagged predators such as sharks and seals help determine whether existing MPAs effectively cover important habitats. 



Studies in the Ross Sea and British Indian Ocean Territory have confirmed that MPAs contribute to the conservation of top marine predators.



<h2 class="wp-block-heading" id="h-a-global-internet-of-animals">A global "Internet of Animals"</h2>



The full potential of biologging depends on worldwide cooperation. 



“The full potential of biologging can only be realized through increased global collaboration and data sharing, enabling the integration of data across <a href="https://www.earth.com/news/animal-size-and-cancer-risk-surprising-new-details-have-emerged/" target="_blank" rel="noreferrer noopener">species</a>, regions, and environmental contexts,” noted Iwata.



The researchers propose creating an “Internet of Animals,” where experts worldwide share biologging data to study marine life on a larger scale.



However, global data access and standardization remain major challenges. The Japanese research team calls for greater collaboration among scientists and data-sharing platforms to overcome these barriers.



<h2 class="wp-block-heading" id="h-expanding-biologging-s-reach">Expanding biologging’s reach</h2>



Iwata hopes this research will encourage more scientists to explore biologging. 



“If we can promote the sharing of biologging data through this paper, I hope to not only recruit more researchers to this field but also to so open up new angles that we haven’t yet envisioned,” he said.



“Researchers are not experts in social implementation, but in recent years, I have seen various issues being solved by sharing data in a data-driven society. It was an enjoyable task to think of ways to return the power of data to society.”



This study was conducted in collaboration with a researcher from <a href="https://www.waseda.jp/top/en/" target="_blank" rel="noreferrer noopener">Waseda University</a>. By promoting biologging and data-sharing, researchers hope to build a stronger foundation for marine conservation efforts.



The study is published in the journal <a href="https://www.sciencedirect.com/science/article/pii/S2772735125000265?via%3Dihub" target="_blank" rel="noreferrer noopener">Water Biology and Security</a>.



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Biologging: Animals are recording human impact on the ocean

Biologging sensors attached to animals help researchers collect valuable data...

Australia’s landscapes are home to one of nature’s most fascinating creatures - the kangaroo. Unique among large animals, kangaroos depend on hopping as their main form of locomotion.



This method of locomotion, known as saltation, allows them to cover vast distances with efficiency and speed. But how did <a href="https://www.earth.com/news/prehistoric-kangaroos-changed-their-diets-to-survive-climate-change/" target="_blank" rel="noreferrer noopener">kangaroos</a> develop this distinctive way of moving?



Understanding their evolutionary history requires looking at their ancestors, particularly the musky rat-kangaroo, the only macropodoid that does not hop.



<h2 class="wp-block-heading" id="h-kangaroo-relatives-that-don-t-hop">Kangaroo relatives that don't hop</h2>



Amy Tschirn is a PhD student and researcher in the <a href="https://www.flinders.edu.au/college-science-engineering" target="_blank" rel="noreferrer noopener">College of Science and Engineering</a> at Flinders University, and co-lead author of the study.



"The musky rat-kangaroo, as the most primitive living macropodoid (a group that includes kangaroos, wallabies, potoroos and bettongs), can offer insight into evolution within the group, including the origin of bipedal hopping locomotion,” said Tschim.



“As the only living macropodoid that doesn’t hop, the musky rat-kangaroo provides a crucial insight into how and when the iconic hopping form of locomotion evolved in Australia.”



Studying the musky rat-kangaroo helps scientists understand how early macropodoids moved before developing bipedal hopping. 



This tiny marsupial, found in the dense rainforests of Queensland, may hold the key to unlocking the evolutionary steps that led to modern <a href="https://www.earth.com/news/protemnodon-kangaroo-fossils-may-explain-their-extinction/" target="_blank" rel="noreferrer noopener">kangaroos</a>.



<h2 class="wp-block-heading" id="h-musky-rat-kangaroos-in-the-wild">Musky rat-kangaroos in the wild</h2>



To study the movement of musky rat-kangaroos, researchers observed them in their natural habitat in the Atherton Tableland, a region in far-northern Queensland. 



By filming adult muskies in the wild, they documented how these animals move and whether any form of hopping appeared in their locomotion. The findings revealed something remarkable.



Unlike any other marsupial that moves on all fours, musky rat-<a href="https://www.earth.com/news/giant-kangaroos-of-the-past-didnt-hop-they-walked-on-all-fours/" target="_blank" rel="noreferrer noopener">kangaroos</a> use a distinct style of movement called a "bound" or "half-bound" gait. This means their hindfeet move together in synchrony rather than alternating as in most quadrupedal animals. 



This movement pattern is unusual among marsupials and could provide crucial insight into how macropodoids transitioned toward hopping.



<h2 class="wp-block-heading" id="h-role-of-quadrupedal-movement">Role of quadrupedal movement</h2>



Observations also confirmed that musky rat-kangaroos never hop, even when moving at their fastest speeds. This means that hopping likely developed later in macropodoid evolution.



“There remains no evidence of hopping in this <a href="https://www.earth.com/news/the-wallace-line-a-natural-border-that-no-species-crosses/" target="_blank" rel="noreferrer noopener">species</a>. Even when travelling at high speeds, muskies always use quadrupedal gaits, never rearing up on just their back legs,” said Harvard’s Dr. Peter Bishop, co-lead author of the research paper.



“These results support the hypothesis that a shift to an asymmetric-gait-dominant locomotor repertoire was a functional prerequisite in the evolution of bipedal hopping in macropodoids.”



Since musky rat-kangaroos lack the ability to hop, scientists believe that the transition toward bipedal movement must have started with an intermediary stage. The bounding gait of these small marsupials may represent a stepping stone in this evolutionary process.



<h2 class="wp-block-heading" id="h-bounding-led-to-hopping-in-kangaroos">Bounding led to hopping in kangaroos</h2>



The musky rat-kangaroo's movement patterns align with previous studies on quadrupedal Australian marsupials. 



Many use symmetric gaits at lower speeds and shift to asymmetric gaits at higher speeds. Unlike most, however, the musky rat-kangaroo exclusively uses asymmetric gaits, even at slow speeds.



Research suggests that early macropodoids likely adopted a bounding gait before transitioning to bipedal hopping. Small potoroids, close relatives of kangaroos, demonstrate this transition by using both quadrupedal bounding and bipedal hopping at different speeds. 



This pattern hints that bounding could have been the crucial precursor to the hopping behavior seen in modern kangaroos.



<h2 class="wp-block-heading" id="h-body-structure-and-the-kangaroo-hop">Body structure and the kangaroo hop</h2>



The musky rat-kangaroo also retains several physical traits that distinguish it from true hopping macropodoids. Its forelimbs and hindlimbs are proportionally closer in size compared to kangaroos, which have much longer hindlimbs adapted for hopping. 



The musky rat-kangaroo also has a mobile first toe, something absent in larger macropodoids. These features suggest that its anatomy is better suited for quadrupedal movement, making it unlikely to develop hopping.



Studies on limb proportions across marsupials and rodents indicate that animals capable of bipedal locomotion generally have shorter forelimbs relative to their hindlimbs. 



The musky rat-kangaroo falls somewhere in between, suggesting it represents an early stage in macropodoid evolution before the full transition to bipedal hopping.



<h2 class="wp-block-heading" id="h-from-bounding-to-hopping">From bounding to hopping</h2>



The transition from quadrupedal movement to bipedal hopping remains one of the most intriguing mysteries of kangaroo evolution. By studying the musky rat-kangaroo’s anatomy and locomotion, researchers can piece together the story of how hopping emerged.



“These results signal a potential pathway to how bipedal hopping evolved in kangaroos. Perhaps it started with an ancestor that moved about on all fours like other marsupials, then an animal that bounded like the muskies, and finally evolved into the iconic hopping kangaroos we see in Australia today.”



This suggests that early macropodoids may have first adopted bounding gaits, allowing them to generate forward momentum using their powerful hind legs. 



Over time, as these animals became more specialized, they may have started relying solely on their back legs, leading to the development of true hopping.



<h2 class="wp-block-heading" id="h-future-of-kangaroo-evolution-studies">Future of kangaroo evolution studies</h2>



The research, published in Australian Mammalogy, provides an important foundation for future studies on kangaroo evolution. 



While the mystery of hopping is still being unraveled, fossil discoveries from early macropodoids could provide more clues about how and when kangaroos made the final leap into bipedal hopping.



Scientists also hope to answer another key question: why did hopping kangaroos grow so much larger than rodents, which also use saltation? Understanding this could reveal more about the evolutionary pressures that shaped Australia’s unique wildlife.



By continuing to study living species like the musky rat-kangaroo and examining fossils from early kangaroo ancestors, researchers move closer to understanding one of the most distinctive adaptations in the animal kingdom.



The study is published in the journal <a href="https://www.publish.csiro.au/AM/AM24050" target="_blank" rel="noreferrer noopener">Australian Mammalogy</a>.



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How did the kangaroo learn to hop? Insights from its smallest relative

Australia’s landscapes are home to one of nature’s most fascinating...

World Frog Day is more than just a date on the calendar - it’s a global wake-up call. For 265 million years, frogs have hopped through Earth’s ever-changing landscapes. 



They outlived dinosaurs, weathered ice ages, and adapted to shifting climates. Yet today, despite their incredible resilience, frogs stand on the brink of disaster.



These small, unassuming creatures do far more than fill the air with their evening croaks. They control insect populations, provide food for countless predators, and serve as nature’s bioindicators because they are sensitive to environmental changes long before these become crises. 



When <a href="https://www.earth.com/news/missing-frog-species-alsodes-vittatus-resurfaces-after-130-years/" target="_blank" rel="noreferrer noopener">frogs</a> start disappearing from an ecosystem, it’s a sign that something is deeply wrong.



Pollution, deforestation, climate change, and the deadly chytrid fungus are driving entire species to extinction at an alarming rate. 



If frog populations continue to decline, the consequences will be catastrophic. Ecosystems will become unbalanced, food chains may collapse, and Earth will lose one of its most ancient inhabitants.



That’s why&nbsp;World Frog Day, observed every&nbsp;March 20&nbsp;since&nbsp;2014, is important. It shines a spotlight on these amphibians, raises awareness about their plight and urges action before time runs out.



<h2 class="wp-block-heading" id="h-why-frogs-matter">Why frogs matter</h2>



Frogs are key players in natural ecosystems. As predators, they feast on mosquitoes, flies, and agricultural pests, helping control populations that could otherwise spiral out of balance.



Without them, farmers would struggle with increased infestations, and diseases spread by insects could become even harder to manage.



On the flip side, frogs themselves are prey for countless creatures; birds, fish, reptiles, and even some mammals rely on them as a food source. If frogs disappear, so do many of the animals that depend on them, which would trigger a domino effect throughout the ecosystem.



Then there’s their role as bioindicators. Healthy frog populations signal healthy environments. But declining frog populations indicate bigger issues - polluted waters, rising temperatures, or habitat destruction, for example. 



<h2 class="wp-block-heading" id="h-frogs-are-facing-many-threats">Frogs are facing many threats </h2>



Despite their adaptability, frogs face an uphill battle for survival, with habitat destruction being the primary threat.



Wetlands are commonly drained for urban expansion and forests are cut down to make way for agriculture. Rivers and lakes are polluted with industrial waste and pesticides. Every time humans encroach on these habitats, frog populations shrink a little more.



Pollution is another major issue. Since <a href="https://www.earth.com/news/walking-on-water-cricket-frogs-redefine-aquatic-locomotion/" target="_blank" rel="noreferrer noopener">frogs</a> absorb water directly through their porous skin, they have no defense against toxins in their environment. Pesticides used in farming leach into nearby ponds and streams, poisoning frogs from the outside in.



Then there’s the chytrid fungus, a disease that has devastated amphibian populations worldwide. It attacks their skin, and prevents them from absorbing water and essential nutrients. Entire species have been wiped out in mere decades by this devastating fungus. 



<h2 class="wp-block-heading" id="h-climate-change-is-making-things-worse">Climate change is making things worse</h2>



As if habitat loss and pollution weren’t enough, <a href="https://www.earth.com/news/frog-saunas-hot-solution-to-fighting-global-amphibian-extinction-apocalypse/" target="_blank" rel="noreferrer noopener">frogs</a> are also battling the effects of climate change. 



Rising temperatures have thrown off their breeding cycles, causing unpredictable shifts in their life stages. Some species, accustomed to stable seasonal patterns, now struggle to find mates or lay eggs at the right time.



Extreme weather events have also taken a toll. In some areas, prolonged droughts have dried up breeding ponds before tadpoles have had a chance to develop. In others, flooding has swept away entire populations. 



<h2 class="wp-block-heading" id="h-the-fight-to-save-the-frogs">The fight to save the frogs</h2>



Despite the grim outlook, conservationists aren’t giving up. Around the world, dedicated researchers and volunteers are working to preserve frog habitats, restore wetlands, and develop captive breeding programs for endangered species. 



In some cases, frogs have been reintroduced into the wild after their populations were nearly wiped out - a small but hopeful sign that efforts can make a difference.



One of the most effective strategies has been the creation of protected areas where <a href="https://www.earth.com/news/frogs-exposed-to-radiation-show-no-signs-of-accelerated-aging/" target="_blank" rel="noreferrer noopener">amphibians</a> can thrive without human interference. These conservation zones shield frogs from pollution, deforestation, and urban expansion, giving them a fighting chance at survival. 



Scientists are also working to combat the chytrid fungus, testing anti-fungal treatments that could slow or stop the spread of infection.



<h2 class="wp-block-heading" id="h-take-action-on-world-frog-day">Take action on World Frog Day</h2>



World Frog Day 2025 presents us with a chance to take action. Across the globe, events will highlight the importance of frog conservation, from educational programs at zoos, to hands-on habitat restoration projects.



The Little Rock Zoo in Arkansas, for example, is set to host special exhibits and talks about amphibian protection. Schools and nature organizations will also join in, organizing workshops and field trips to explore local frog populations.



But you don’t need to attend an event to make a difference. Learning about the different species of frogs in your region is a good start. Avoiding pesticides and herbicides in your garden helps protect their habitats. Creating a frog-friendly space with native plants, small ponds, or log shelters can provide much-needed refuge.



If you want to do more, consider supporting conservation organizations. Donations help fund research, breeding programs, and habitat restoration efforts. Volunteering for local environmental groups can also put you on the frontlines of conservation work.



You can even virtually adopt a tree frog through the <a href="https://gifts.worldwildlife.org/gift-center/gifts/species-adoptions/red-eyed-tree-frog?srsltid=AfmBOorRwjDH5ydXRC_2hQV_O2f5MO1PjHWAutpoeSOhQp7kn7mTcs6P" target="_blank" rel="noreferrer noopener">World Wildlife Fund</a>.



<h2 class="wp-block-heading" id="h-a-world-without-frogs">A world without frogs?</h2>



The loss of frogs isn’t just an ecological disaster - it’s a warning. Their decline signals deeper problems in our environment, problems that will eventually affect humans too. 



If frogs disappear, it means our water is more polluted, our ecosystems are out of balance, and the natural world is in crisis.



World Frog Day reminds us that their survival is tied to our own. By protecting them, we protect ourselves and the planet we share. Whether it’s through education, activism, or simple everyday choices, everyone can contribute to this effort. 



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World Frog Day 2025: Protecting nature’s tiny guardians

World Frog Day is more than just a date on...

A recent study has discovered a surprising behavior in lemon leafcutter ants (Atta sexdens). These ants not only exhibit social immunity - the ability to detect and remove pathogens to protect their colony - but also appear to remember past infections and respond more aggressively to familiar threats.



The research, led by <a href="https://www.international.unesp.br/" target="_blank" rel="noreferrer noopener">São Paulo State University</a> (UNESP), reveals that leafcutter ants can recognize a pathogenic fungus they have previously encountered, even 30 days after the initial exposure. 



When re-exposed, they intensify their cleaning behaviors and recruit more workers, a phenomenon researchers suggest could be considered a form of “social immune memory.”



<h2 class="wp-block-heading" id="h-a-superorganism-s-defense-mechanism">A superorganism’s defense mechanism</h2>



“If we think of the <a href="https://www.earth.com/news/larger-ant-colonies-drove-the-evolution-of-worker-castes/" target="_blank" rel="noreferrer noopener">colony</a> as a superorganism, these behaviors would be like the immune system,” said first author Aryel Goes, a former bioscience student at UNESP. “In the same way that our defense cells attack invaders, such as viruses and bacteria, the workers fight infections that could harm the colony.”



The study shows that, unlike individual <a href="https://www.earth.com/news/covid-19-lockdowns-weakened-our-immune-systems/" target="_blank" rel="noreferrer noopener">immune systems</a> in animals, ants respond to infections collectively.&nbsp;



“What we’re showing is that the social immune system of ants can store information about previous infections with the same pathogen, a phenomenon seen in our immune cells, but which occurs at a behavioral level in ant colonies,” Goes said.



To test this idea, the researchers conducted several experiments to observe how ants responded to repeated exposures to the same pathogen.



<h2 class="wp-block-heading" id="h-a-stronger-response-to-familiar-threats">A stronger response to familiar threats</h2>



In one experiment, the team exposed <a href="https://www.earth.com/news/dinosaur-extinction-led-to-the-emergence-of-ant-agriculture/" target="_blank" rel="noreferrer noopener">ant colonies</a> to a pathogen, then reintroduced it after seven days and again after a month. The ants' response became significantly stronger over time, with the most intense reaction occurring at the 30-day mark. 



More ants participated in cleaning activities, both grooming themselves and removing the harmful fungus from the fungi they cultivate for food.



Lemon leafcutters belong to a group of ants that maintain a mutualistic relationship with fungi, cultivating them inside their colonies as a food source. In return, the fungi provide essential nutrients for the ants.



As part of the study, researchers tested four different pathogens - two harmful to the ants themselves and two that targeted their cultivated <a href="https://www.earth.com/news/fungus-farming-ants-work-hard-to-maintain-healthy-gardens/" target="_blank" rel="noreferrer noopener">fungi</a>.&nbsp;



In another experiment, the scientists exposed separate colonies to a pathogen, then reintroduced it after seven days and again after 60 days. This time, the ants' responses were noticeably weaker compared to those that encountered the pathogen after 30 days.



“Unlike our immune system, which in some cases responds expressively to a specific pathogen even many years after initial exposure, ants’ social immune memory has a shorter time frame, so they need to be constantly exposed to the pathogen for the information to persist,” explained Goes.



<h2 class="wp-block-heading" id="h-do-ants-recognize-specific-pathogens">Do ants recognize specific pathogens?</h2>



The researchers also tested whether the ants' memory-like response was pathogen-specific. In a third experiment, they exposed the ants to one pathogen, then introduced a different pathogen after seven days. The ants' response to the second pathogen was much weaker than their reaction to the original one.



The following week, the researchers reintroduced the first pathogen. While the ants reacted, their response was only moderate - similar to their first encounter with the pathogen, but far less intense than when the pathogen had been reintroduced after 30 days.



Rodrigues suggested that this behavior could be a strategy to prevent accidentally spreading a new pathogen within the colony. “One hypothesis is that the lemon leafcutter reduced its hygienic response to avoid spreading the new pathogen to the rest of the colony.&nbsp;



This is because cleaning altruism, in which ants lick each other to get rid of pathogens, can also spread new contaminants. That’s why they would have been more careful with a second infection that was completely new to the colony,” he explained.



<h2 class="wp-block-heading" id="h-do-ants-respond-to-unknown-substance">Do ants respond to unknown substance?</h2>



To ensure that the ants’ response was indeed triggered by pathogens and not simply by exposure to an unfamiliar substance, the researchers applied a harmless solution to five colonies as a control.&nbsp;



The ants in this group showed the weakest response of all the experiments, suggesting that the ants can distinguish between different substances and respond more aggressively to harmful pathogens.



The study raises the possibility that social immunity in leafcutter ants could increase the efficiency of pathogen removal, improving the colony’s overall survival. However, more research is needed to determine whether this actually qualifies as a form of immune memory.



<h2 class="wp-block-heading" id="h-implications-for-pest-control">Implications for pest control</h2>



Leafcutter ants, including Atta sexdens, thrive in open environments and have adapted well to agricultural landscapes, making them a common <a href="https://www.earth.com/news/urgent-need-to-protect-earths-forests-from-non-native-pests/" target="_blank" rel="noreferrer noopener">pest</a> in monoculture farming.&nbsp;



Their strong cleaning behaviors pose a challenge to biological control methods that rely on natural pathogens rather than chemical pesticides.



“Lemon leafcutters are adapted to open areas, so they benefit from monocultures and are a pest. Their cleaning behavior is one of the obstacles to effective biological control without the use of chemical insecticides. Understanding the social immunity of leafcutters can help to develop more effective and ecologically correct controls,” Rodrigues concluded.



The study is published in the journal <a href="http://dx.doi.org/10.1098/rspb.2024.1097" target="_blank" rel="noreferrer noopener">Proceedings of the Royal Society B</a>.



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Leafcutter ants remember past infections, strengthening colony defenses

A recent study has discovered a surprising behavior in lemon...

For more than 20 years, scientists have puzzled over an unusual trait in thorny skates in the North Atlantic. 



In some parts of their range, these fish appear in two distinctly different sizes, regardless of their sex. Researchers were unable to determine the cause of this phenomenon - until now.



A new study led by Jeff Kneebone and a team from the <a href="https://www.floridamuseum.ufl.edu/" target="_blank" rel="noreferrer noopener">Florida Museum of Natural History</a> has finally solved the mystery, thanks in part to unexpected disruptions caused by the COVID-19 pandemic.



<h2 class="wp-block-heading" id="h-a-longstanding-conservation-puzzle">A longstanding conservation puzzle</h2>



The size discrepancy among thorny skates has been noted for nearly a century, but the issue became especially significant in the 1970s when their populations began to plummet. Suspecting <a href="https://www.earth.com/news/overfishing-has-caused-a-50-decline-in-sharks-and-rays/" target="_blank" rel="noreferrer noopener">overfishing</a> as the main culprit, authorities implemented a strict fishing ban on thorny skates and barndoor skates in 2003.



“The barndoor skate rebounded to the point where they’re now allowed to be harvested again, but for whatever reason, the thorny skate has remained low, despite 20 years of protection,” said Kneebone, a senior scientist at the <a href="https://www.neaq.org/conservation-and-research/anderson-cabot-center-for-ocean-life/" target="_blank" rel="noreferrer noopener">Anderson Cabot Center for Ocean Life</a> at the New England Aquarium.



Data from the <a href="https://www.noaa.gov/" target="_blank" rel="noreferrer noopener">National Oceanic and Atmospheric Administration</a> indicates that thorny skate populations have declined by 80% to 95% in some regions, particularly in the Gulf of Maine and Canadian waters off the Scotian Shelf.



<h2 class="wp-block-heading" id="h-the-mystery-of-thorny-skates">The mystery of thorny skates </h2>



Thorny skates have an extensive distribution, ranging from South Carolina to the Arctic Circle and across to Europe and Russia. However, the size variation appears to be unique to North American waters; in the Arctic and Europe, thorny skates only appear in one size.



“No one could understand what the deal was with these skates,” said study co-author Gavin Naylor, director of the <a href="https://www.floridamuseum.ufl.edu/sharks/" target="_blank" rel="noreferrer noopener">Florida Program for Shark Research</a> at the Florida Museum of Natural History. 



Researchers had previously analyzed thorny skate DNA, searching for genetic differences between the two size variants, but found nothing.&nbsp;



“The big forms are twice the size, and it takes them 11 years to reach adulthood. The small forms are mature by the time they’re six years old. There’s got to be genetic differences.”



Naylor believed a more detailed genetic analysis could uncover the answer.



<h2 class="wp-block-heading" id="h-samples-from-hundreds-of-thorny-skates">Samples from hundreds of thorny skates </h2>



Previous attempts to solve the mystery involved sequencing short DNA fragments from a small number of individuals.&nbsp;



While a reasonable approach, Naylor suspected it had failed because not enough of the genome had been examined. Instead, he proposed a gene capture method, an intensive approach that collects DNA sequences from thousands of genes across an organism’s <a href="https://www.earth.com/news/how-does-genome-size-impact-evolutionary-success/" target="_blank" rel="noreferrer noopener">genome</a>.&nbsp;



This would require analyzing samples from hundreds of thorny skates to gather a comprehensive dataset.



Researchers from around the world responded to Naylor’s request for samples, providing more than 600 tissue specimens spanning much of the Northern Hemisphere and helping him prepare for an extensive lab analysis.



Then, the <a href="https://www.earth.com/news/hidden-death-toll-of-covid-19-pandemic-revealed/" target="_blank" rel="noreferrer noopener">COVID-19 pandemic</a> shut down lab operations, halting their work indefinitely.



At that point, postdoctoral researcher Shannon Corrigan devised an alternative plan. Instead of conducting a labor-intensive gene capture study on hundreds of skates, they would sequence the full genome of just a handful - four or five individuals. While less comprehensive, it would still allow them to search for significant genetic differences.



It was a gamble. If the genome sequencing approach failed, the team would have used up their funding with no results.



“It was a Hail Mary,” Naylor said. But it paid off. In fact, had they stuck with the original plan, “we would have missed it entirely.”



<h2 class="wp-block-heading" id="h-a-key-genetic-difference">A key genetic difference</h2>



The breakthrough came when lead author Pierre Lesturgie analyzed the genome - comprising 2.5 billion base pairs. As he sifted through the data, he noticed something unusual.



“There was a large region on chromosome two that we thought was weird. Since it was behaving in a way we didn’t understand, we considered removing it from the analysis,” Lesturgie said.



Initially, he suspected the anomaly was a sequencing error and worried it might skew their results. But before discarding it, Naylor recognized a pattern - it resembled a gene inversion, where a segment of DNA is flipped in the opposite direction.



Gene inversions are common across many species, including humans, but they rarely result in such dramatic physical differences. Still, the team decided to check if this inverted DNA sequence was present in both small and large thorny skates.



It wasn’t. Only the larger skates had the inversion. They had finally uncovered the genetic basis for the size difference.



<h2 class="wp-block-heading" id="h-implications-for-conservation">Implications for conservation</h2>



Now that scientists understand why thorny skates appear in two distinct sizes, Kneebone believes they can develop more effective conservation strategies.&nbsp;



The next step is to study the skates' life histories more closely - something that has been challenging due to the difficulty of distinguishing between the two types.



“We could identify the large males and females because they’re bigger than anything else,” Naylor said. Both large and small males develop distinctive long claspers on either side of their tails when they reach maturity.&nbsp;



“So when you’ve got a small male with large claspers, we know it’s an adult. But we can’t do anything with the small females because we don’t know whether they’re just babies on their way to getting big.”



This has complicated research on the species. “The big question has always been, what do the life histories of the two morphs look like? Currently, they’re not discriminated in the stock assessment, so a thorny skate is a thorny skate is a thorny skate,” Kneebone said.



<h2 class="wp-block-heading" id="h-the-role-of-climate-change">The role of climate change</h2>



Even with this discovery, thorny skates are still struggling in parts of their range, particularly in the Gulf of Maine. One potential factor is <a href="https://www.earth.com/news/climate-change-is-impacting-marine-life-more-than-we-realized/" target="_blank" rel="noreferrer noopener">climate change</a>.



Current evidence suggests that the two size variants may have difficulty interbreeding in areas where populations are declining. Warming ocean temperatures could be exacerbating this natural reproductive barrier.



The Gulf of Maine has experienced some of the fastest ocean warming on the planet, with sea surface temperatures rising at a rate faster than 99% of the world's oceans. This has already led to significant ecological changes, such as the collapse of cod fisheries.



Scientists are now investigating whether climate change is disproportionately affecting thorny skates compared to other skate species in the region.



“We’re trying to use the best available science to make decisions about how to best manage and sustain populations,” Kneebone concluded.



The study is published in the journal <a href="http://dx.doi.org/10.1038/s41467-025-56126-z" target="_blank" rel="noreferrer noopener">Nature Communications</a>.



Image Credit: Illustration by Jorge Machuski



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DNA twist reveals why some thorny skates grow twice as large

For more than 20 years, scientists have puzzled over an...

Since the Industrial Revolution, the world has witnessed a sharp increase in noise pollution generated by human activities. Whether it’s the constant hum of traffic, airplanes overhead, or the repetitive clamor of construction, these sounds can obstruct animals’ abilities to give and receive crucial signals - a process that is fundamental to their survival and reproduction.



Now, a team of biologists at the <a href="https://www.unl.edu/" target="_blank" rel="noreferrer noopener">University of Nebraska–Lincoln</a> (UNL) has published one of the first known studies demonstrating how one group of animals can react to human-made noise by adjusting its own method of sensing sounds.&nbsp;



In an article published in the journal <a href="https://dx.doi.org/10.1016/j.cub.2025.02.041" target="_blank" rel="noreferrer noopener">Current Biology</a>, researchers Brandi Pessman and Eileen Hebets show that funnel-weaving <a href="https://www.earth.com/news/spiders-reveal-how-cave-creatures-lose-their-vision-over-time/" target="_blank" rel="noreferrer noopener">spiders</a> alter how their silk webs transmit vibrations in response to local noise. 



This finding suggests that the spiders might deliberately change web structure to cope with the auditory chaos surrounding them, ensuring they receive vital cues from potential mates, prey, or predators.



<h2 class="wp-block-heading" id="h-a-key-discovery-about-web-adjustments">A key discovery about web adjustments</h2>



Drawing on lab experiments, the study uncovered a particularly unexpected insight: the way a spider’s web conveys vibrations varies depending on whether its architect was collected from a rural or urban area. This discrepancy hints at the idea that prior exposure to noise - possibly even inherited across generations - may influence a spider’s malleability when it comes to spinning webs.



“One of the most interesting things that we found is that urban and rural spiders are reacting differently when they're put into a noisy environment,” said Pessman, a postdoctoral researcher in biological sciences and the lead author of the paper. 



“This means that spiders with different experiences with noise - whether they themselves experienced it or their mothers passed it down to them across generations - respond differently.”



<h2 class="wp-block-heading" id="h-spider-webs-as-sensory-extensions">Spider webs as sensory extensions</h2>



It has been well documented that animals such as birds and <a href="https://www.earth.com/news/climate-change-is-altering-the-calls-and-voices-of-frogs-around-the-world/" target="_blank" rel="noreferrer noopener">frogs</a> can change their calls or the timing of their vocalizations in the face of increased human noise. However, little was known about how animals manage to tweak the way they receive acoustic or vibratory signals. 



The main challenge is the hidden nature of most animals’ sensory systems, which are located within their bodies. But web-building spiders are unique, as their webs function effectively like external sensory extensions that capture vibrations from the environment.



This distinction makes funnel-weaving spiders, also known as Agelenopsis pennsylvanica, an ideal test group. They rely predominantly on vibratory signals for vital information. Their webs connect to various surfaces - trees, rocks, or buildings - capable of transmitting the vibratory noise created by <a href="https://www.earth.com/news/some-birds-get-road-rage-when-exposed-to-traffic-noise/" target="_blank" rel="noreferrer noopener">traffic</a>, industrial activities, and more.&nbsp;



The research team hypothesized that funnel-weaving spiders might be able to reduce the volume of unwanted or irrelevant vibrations caused by human-related noise, which often shares the frequency range these spiders need for effective communication.



<h2 class="wp-block-heading" id="h-spiders-in-urban-areas">Spiders in urban areas</h2>



Pessman started by collecting a total of 60 funnel-weaving spiders in and around Lincoln, Nebraska - some from city settings and others from out in the countryside. In the lab, the spiders were then placed in controlled environments that were either quiet or noisy as they spun webs over four nights. 



Upon completion, the researchers introduced test vibrations into those webs, measuring how energy moved across the silk in different conditions.



They observed that spiders from urban areas tended to build webs that lost more energy in short-distance vibrations across a broader set of frequencies when placed under noisy conditions. 



Interpreted practically, these webs essentially “muffled” environmental noise. This may prevent sensory overload, giving the spiders a clearer signal from <a href="https://www.earth.com/news/largest-predator-prey-feast-ever-seen-in-the-ocean-enormous-quickly-altered-food-chain/" target="_blank" rel="noreferrer noopener">prey</a> or other relevant vibrations in their immediate vicinity.



<h2 class="wp-block-heading" id="h-spiders-that-are-exposed-to-less-noise">Spiders that are exposed to less noise</h2>



Meanwhile, rural spiders assembled their webs in such a way that energy from biologically important long-distance vibrations was preserved. This indicates they might be amplifying or enhancing certain frequency ranges to pick out meaningful vibrations above the background noise.



“Rural spiders are not used to as much noise in their environment,” Pessman said. “When they suddenly get a lot of noise, they might try to 'turn up' the volume in their webs or amplify what's coming in to better hear certain signals above the noise.”



<h2 class="wp-block-heading" id="h-implications-for-ecology-and-future-studies">Implications for ecology and future studies</h2>



Given the role of funnel webs as external sensory structures, these findings open a new window into how animals can adjust the way they receive signals, a research area that had remained largely unclear until now. 



The ability to alter web structure in response to different noise environments could prove vital as human-made noise continues to escalate across the planet.



In the future, the team plans to investigate precisely how the spiders are changing their webs - whether they adjust the tension of certain silk lines, vary anchor points, or adopt an entirely new shape to filter or boost specific frequencies. 



High-speed video of the web-building process, combined with digital tracking methods, will let them delve deeper into these construction nuances.



<h2 class="wp-block-heading" id="h-spiders-overcoming-environmental-noise">Spiders overcoming environmental noise</h2>



“This study really highlights the role of receivers in overcoming environmental noise,” said Hebets, who is a professor of biological sciences at UNL. 



“It opens up entirely new avenues of research. For example, are receivers placing themselves at certain locations in the environment where signals are going to receive less attenuation or overlap of noise?”



By revealing that some species can modify their “sensor” for hearing, the team hopes to inspire more research on how other animals cope with rising noise levels. 



The funnels built by these little invertebrates may seem inconsequential to an urban passerby, but as the study shows, each strand of silk can be precisely tuned to help the spider thrive in a clamorous world.



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Spiders adapt their webs to filter out human-made noise

Since the Industrial Revolution, the world has witnessed a sharp...

A Deep-Sea Sponge and Anemones in Antarctica

An international team of researchers took advantage of a rare chance encounter to explore a massive new expanse of seafloor exposed by the breakup of an Antarctic ice shelf in the Bellingshausen Sea.&nbsp;



On January 13, 2025, an iceberg named A-84 - which was the size of the city of Chicago - broke off from the George VI Ice Shelf, which sits along the Antarctic Peninsula. 



This event uncovered roughly 209 square miles (540 square kilometers) of seafloor that had previously been concealed under floating ice.



The team arrived aboard <a href="https://schmidtocean.org/" target="_blank" rel="noreferrer noopener">Schmidt Ocean Institute</a>’s R/V Falkor (too) at this newly exposed site on January 25, making them the first to study such a large underwater area that had previously been covered by an ice shelf.&nbsp;



Their effort marks the first large-scale interdisciplinary exploration of geologic, oceanographic, and biological features hidden beneath an extensive floating <a href="https://www.earth.com/news/astonishing-glacier-retreat-in-the-arctic-signals-climate-disaster/" target="_blank" rel="noreferrer noopener">glacier</a> front.



<h2 class="wp-block-heading" id="h-rapidly-shifting-expedition-goals">Rapidly shifting expedition goals</h2>



Co-chief scientist Patricia Esquete is a researcher in the <a href="https://www.cesam-la.pt/en/" target="_blank" rel="noreferrer noopener">Center for Environmental and Marine Studies</a> (CESAM) and the Department of Biology (DBio) at the <a href="https://www.ua.pt/" target="_blank" rel="noreferrer noopener">University of Aveiro</a> in Portugal.&nbsp;



"We seized upon the moment, changed our expedition plan, and went for it so we could look at what was happening in the depths below,” said Esquete.



“We didn’t expect to find such a beautiful, thriving <a href="https://www.earth.com/news/how-environmental-stress-strengthens-ecosystems/" target="_blank" rel="noreferrer noopener">ecosystem</a>. Based on the size of the animals, the communities we observed have been there for decades, maybe even hundreds of years.”



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/03/Antarctic-iceberg-detached_seafloor-study_credit-SOI_1m.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/03/Antarctic-iceberg-detached_seafloor-study_credit-SOI_1s.webp" alt="The newly exposed Antarctic seafloor also allowed the team to gather critical data on the past behavior of the ice sheet. The ice sheet has been shrinking and losing mass over the last few decades due to climate change. Credit: Alex Ingle / Schmidt Ocean Institute" class="wp-image-1963228"/></a><figcaption class="wp-element-caption">The newly exposed Antarctic seafloor also allowed the team to gather critical data on the past behavior of the ice sheet. The ice sheet has been shrinking and losing mass over the last few decades due to climate change. Credit: Alex Ingle / Schmidt Ocean Institute</figcaption></figure>



Originally, the science mission did not include venturing beneath a freshly fractured portion of the ice shelf. 



However, the movement of this newly calved <a href="https://www.earth.com/news/massive-iceberg-that-broke-away-from-antarctica-sparks-concerns/" target="_blank" rel="noreferrer noopener">iceberg</a> offered a rare opportunity to explore a site that, until recently, had never been examined by any human.



<h2 class="wp-block-heading" id="h-antarctic-seafloor-reveals-lush-communities">Antarctic seafloor reveals lush communities</h2>



Using Schmidt Ocean Institute’s remotely operated vehicle, ROV SuBastian, the science team spent eight days surveying the seafloor at depths down to 1,300 meters (4,265 feet).&nbsp;



The experts discovered an unexpectedly rich ecosystem that was teeming with corals, sponges, icefish, giant sea spiders, and <a href="https://www.earth.com/news/octopuses-could-dominate-earth-if-humans-vanish/" target="_blank" rel="noreferrer noopener">octopuses</a> - an indication that marine life can flourish under ice-covered regions of the Antarctic in ways not previously documented.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/03/Antarctic-iceberg-detached_seafloor_octopus-resting_credit-SOI_1m.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/03/Antarctic-iceberg-detached_seafloor_octopus-resting_credit-SOI_1s.webp" alt="An octopus rests on the seafloor 1150 meters deep, in the Bellingshausen Sea off Antarctica, at an area where the shelf break and slope are cut by several underwater gullies. Credit: ROV SuBastian / Schmidt Ocean Institute" class="wp-image-1963224"/></a><figcaption class="wp-element-caption">An octopus rests on the seafloor 1150 meters deep, in the Bellingshausen Sea off Antarctica, at an area where the shelf break and slope are cut by several underwater gullies. Credit: ROV SuBastian / Schmidt Ocean Institute</figcaption></figure>



According to the researchers, these observations offer insight into how ecosystems function beneath the Antarctic ice sheet. Such an ecosystem has seldom been accessed. 



Earlier findings, notably by <a href="https://www.bas.ac.uk/" target="_blank" rel="noreferrer noopener">British Antarctic Survey</a> researchers in 2021, revealed possible bottom-dwelling life beneath ice, but the present study marks the first time an ROV survey has thoroughly documented wide areas of this vibrant seabed.



The experts were surprised by the large biomass and biodiversity in the ecosystem and suspect they have discovered several new species.



<h2 class="wp-block-heading" id="h-how-marine-life-survives-in-darkness">How marine life survives in darkness</h2>



Deep-sea ecosystems generally depend on nutrients trickling down from surface waters. However, these Antarctic seafloors had been buried under ice some 150 meters (nearly 500 feet) thick for centuries.&nbsp;



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/03/Antarctic-iceberg-detached_seafloor_Sponge_Anemone_credit-SOI_1m.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/03/Antarctic-iceberg-detached_seafloor_Sponge_Anemone_credit-SOI_1s.webp" alt="A large sponge, a cluster of anemones, and other life is seen nearly 230 meters deep at an area of the seabed that was very recently covered by the George VI Ice Shelf, a floating glacier in Antarctica. Credit: Schmidt Ocean Institute" class="wp-image-1963226"/></a><figcaption class="wp-element-caption">A large sponge, a cluster of anemones, and other life is seen nearly 230 meters deep at an area of the seabed that was very recently covered by the George VI Ice Shelf, a floating glacier in Antarctica. Credit: Schmidt Ocean Institute</figcaption></figure>



With no direct sunlight, how such abundant organisms manage to feed is still uncertain. The scientists propose that ocean currents under the ice may be funneling essential nutrients to these communities.



<h2 class="wp-block-heading" id="h-antarctic-ice-sheet-behavior">Antarctic ice sheet behavior</h2>



Apart from their ecological discoveries, the international group - which included scientists from Portugal, the United Kingdom, Chile, Germany, Norway, New Zealand, and the United States - examined geological samples to gain knowledge about past changes in the Antarctic ice sheet.



The ice sheet has been shrinking and losing mass for decades in response to climate change.&nbsp;



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/03/Antarctic-iceberg-detached_modis-satellite-view_NASA_1m.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/03/Antarctic-iceberg-detached_modis-satellite-view_NASA_1s.webp" alt="The MODIS Corrected Reflectance satellite imagery showing the iceberg calved from George VI Ice Shelf in the Bellingshausen Sea on 19 January 2025. Credit: Schmidt Ocean Institute" class="wp-image-1963222"/></a><figcaption class="wp-element-caption">The MODIS Corrected Reflectance satellite imagery showing the iceberg calved from George VI Ice Shelf in the Bellingshausen Sea on 19 January 2025. Credit: Schmidt Ocean Institute</figcaption></figure>



“The ice loss from the Antarctic Ice Sheet is a major contributor to sea level rise worldwide,” said co-chief scientist Sasha Montelli of <a href="https://www.ucl.ac.uk/" target="_blank" rel="noreferrer noopener">University College London</a>, who is also a 2019 Schmidt Science Fellow.&nbsp;



“Our work is critical for providing longer-term context of these recent changes, improving our ability to make projections of future change - projections that can inform actionable policies. We will undoubtedly make new discoveries as we continue to analyze this vital data.”



<h2 class="wp-block-heading" id="h-samples-from-the-antarctic-seafloor">Samples from the Antarctic seafloor </h2>



During this mission, the team collected both biological and geological samples. 



In addition, they deployed autonomous underwater vehicles, called gliders, to analyze how meltwater from the ice shelf impacts the region’s physical and chemical properties. 



Preliminary measurements hinted at high biological productivity and strong meltwater flow from the George VI ice shelf, providing further context for how such deep-sea populations may thrive in these surroundings.



<h2 class="wp-block-heading" id="h-part-of-a-larger-global-initiative">Part of a larger global initiative</h2>



The expedition is part of Challenger 150, a global cooperative dedicated to deep-sea biological study, and recognized by the Intergovernmental Oceanographic Commission of UNESCO (<a href="https://www.ioc.unesco.org/en" target="_blank" rel="noreferrer noopener">IOC/UNESCO</a>) as an Ocean Decade Action. 



This alignment ensures that findings from the George VI Ice Shelf breakage feed into broader international efforts to understand and safeguard <a href="https://www.earth.com/news/climate-change-is-impacting-marine-life-more-than-we-realized/" target="_blank" rel="noreferrer noopener">marine life</a>.



“The science team was originally in this remote region to study the seafloor and ecosystem at the interface between ice and sea,” noted Schmidt Ocean Institute’s executive director, Jyotika Virmani.&nbsp;



“Being right there when this iceberg calved from the ice shelf presented a rare scientific opportunity. Serendipitous moments are part of the excitement of research at sea - they offer the chance to be the first to witness the untouched beauty of our world.”



Looking ahead, the researchers plan to continue analyzing the collected data for insights into both ice sheet behavior and the unique marine life that has flourished unseen for centuries beneath the ice.&nbsp;



With accelerating climate change, the study’s findings about species adaptability and the resilience of Antarctic habitats carry implications for future conservation and policy decisions on a global scale.



<a href="https://schmidtocean.photoshelter.com/galleries/C0000QszlkoaNkKU/G0000p4LRtGEAfWo/I0000X_S5KjUr4QU/FKt250110-20250126-IceScanningCollectionAndIcebergViewing-Ingle-0202-jpg" target="_blank" rel="noreferrer noopener">See more of the photos taken on this mission by the Schmidt Ocean Institute here...</a>



Images Credit: Schmidt Ocean Institute



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Iceberg break from Antarctica reveals seafloor full of rare and vibrant ocean creatures

An international team of researchers took advantage of a rare...

Dogs can’t speak, but they express themselves clearly through body language. A bark, a tail wag, or a growl can reveal their feelings, but to understand them better, we must learn to interpret their silent cues.



"Understanding our dogs' basic body language allows us to gain insight into their thoughts and feelings about the world around them and what they are experiencing," said Harmony Diers, a veterinary technician and project manager for the Dog Aging Project at the Texas A&amp;M <a href="https://vetmed.tamu.edu" target="_blank" rel="noreferrer noopener">College of Veterinary Medicine</a> and Biomedical Sciences.



Diers explains how common behaviors can help us understand what our <a href="https://www.earth.com/news/national-puppy-day-2025-where-happiness-meets-responsibility/" target="_blank" rel="noreferrer noopener">dogs</a> are trying to communicate.



<h2 class="wp-block-heading" id="h-signs-of-a-relaxed-dog">Signs of a relaxed dog</h2>



Relaxed <a href="https://www.earth.com/news/how-dogs-feel-smells-may-help-keep-us-safe/" target="_blank" rel="noreferrer noopener">dogs</a> show it with their entire body. Their ears may lean forward or rest gently backward. Sometimes, submissive dogs fold their ears back, but the overall signal is calmness.



One clear sign of happiness is a circular tail wag. If your dog moves its tail in a loop, that shows true joy.



You may also notice soft, squinting eyes, a steady and kind gaze, leaning against you, lying down peacefully, rolling over for belly rubs, or panting with a slightly open mouth.



"It is important to recognize a calm and content <a href="https://www.earth.com/news/petting-a-dog-might-be-the-easiest-way-to-reduce-stress/" target="_blank" rel="noreferrer noopener">dog</a>'s body language to determine whether he or she is comfortable with the current environment and circumstances," Diers explained.



Understanding these signs helps you support your dog without overwhelming it or ignoring its comfort.



<h2 class="wp-block-heading" id="h-when-dogs-want-distance">When dogs want distance</h2>



Not all body language signals comfort. Discontented <a href="https://www.earth.com/news/from-wolves-to-dogs-did-domestication-begin-without-human-help/" target="_blank" rel="noreferrer noopener">dogs</a> often try to create space when feeling stressed.



A tucked tail usually indicates fear. A dog on high alert might raise its tail and wag it quickly, signaling tension rather than joy.



"A dog experiencing an uncomfortable situation may also turn his body away from the threat to present his back," Diers said.



Dogs sometimes shake their entire bodies after a stressful moment, similar to drying off after a bath. This helps them release built-up tension.



Ears held straight up can show readiness for action, while ears pinned close to the head show nervousness or submission. 



If your <a href="https://www.earth.com/news/humans-and-dogs-share-genes-linked-to-obesity/" target="_blank" rel="noreferrer noopener">dog</a> stares intensely or shows the whites of its eyes - often called the "whale eye" - it may be feeling scared or trapped. Tension in the mouth, pulled lips, licking, or yawning can all be signs of stress.



Learning these signals helps protect your dog and others, especially when meeting unfamiliar dogs or entering new spaces.



<h2 class="wp-block-heading" id="h-body-language-varies-by-breed">Body language varies by breed</h2>



Some breeds naturally appear alert, even when relaxed. Recognizing your dog’s baseline posture is important.



"When these dogs are in alert mode or feel threatened, the tail may go higher and stiffer and wag quickly," Diers said. For instance, German shepherds often have upright ears by nature. Huskies and malamutes usually carry curled tails, even when relaxed.



"Look at our pugs. They always have big open eyes, but if a wide-eyed pug is giving the whale eye, he may be experiencing a threat or feeling nervous."



Knowing your dog’s unique structure will help you tell the difference between comfort and caution.



<h2 class="wp-block-heading" id="h-illness-can-alter-body-language">Illness can alter body language</h2>



Body language doesn’t only reflect emotion. It can also signal health issues.



"An ill dog may sleep more, be grumpier and not want the normal interaction he usually gets excited about," Diers said.



A dog in pain might limp, lower its head, keep its posture stiff, tuck its belly inward, or arch its back. Whimpering may also occur. Lip-smacking could mean nausea or nervousness.



If your lively dog suddenly isolates, eats less, or shows no interest in play, something might be wrong.



"Ultimately, if your normally active and happy dog starts to isolate and show lethargy and/or decreased appetite, this is a sign that something has changed with their overall health, and seeking the care of a veterinarian is a suggested course to take," stressed Diers.



Paying attention to your dog’s body language strengthens your relationship. You build trust when you listen to their unspoken signals. Understanding what they say without words keeps them safe, happy, and healthy - and brings you even closer.



Information supplied by <a href="https://phys.org/partners/texas-a-m-university/">Texas A&amp;M University</a>.



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Want to know how your dog is feeling? Learn their body language

Dogs can’t speak, but they express themselves clearly through body...

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