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

A new fossil skull, dug out of purple siltstone in northern China, belongs to a creature that walked the planet about 259 million years ago. The animal was named Yinshanosaurus angustus, and the find helps fill a gap in the family tree of large plant‑eating reptiles that roamed just before the greatest die‑off in Earth’s history.



<h2 class="wp-block-heading" id="h-unearthing-yinshanosaurus-angustus">Unearthing Yinshanosaurus angustus</h2>



<a href="https://www.researchgate.net/profile/Jian-Yi-9" target="_blank" rel="noreferrer noopener">Dr. Jian Yi</a> and <a href="https://www.researchgate.net/profile/Jun-Liu-222" target="_blank" rel="noreferrer noopener">Dr. Jun Liu</a> of the Institute of Vertebrate Paleontology and Paleoanthropology at the Chinese Academy of Sciences (<a href="http://english.ivpp.cas.cn/" target="_blank" rel="noreferrer noopener">IVPP</a>), compared two well‑preserved specimens from Shanxi and Inner Mongolia.



Both fossils include almost complete skulls, giving researchers a rare full view of the head and much of the spine.



“Pareiasauria are a bizarre herbivorous clade of tetrapods that existed in the Guadalupian and Lopingian and were victims of both the <a href="https://www.frontiersin.org/journals/earth-science/articles/10.3389/feart.2021.631198/full" target="_blank" rel="noreferrer noopener">Late Capitanian</a> and the end‑Permian mass extinction events,” reminded Liu. 



The more complete of the two skulls measures 10 inches long yet barely 4 inches wide across the cheeks, the narrowest head known for any pareiasaur.



That unusual shape is not the only odd trait. The snout is as wide as it is high, the frontal bone is slender and twice as long as it is wide, and the upper‑jaw teeth stand almost vertical instead of tilting backward as in relatives.



<h2 class="wp-block-heading" id="h-what-on-earth-is-a-pareiasaur">What on Earth is a pareiasaur?</h2>



A pareiasaur is a stocky, barrel‑bodied tetrapod that carried a tiny tail and a head often ringed with bony knobs. Most species topped out at about 8 feet long and weighed as much as today’s American bison.



They thrived across the <a href="https://pubmed.ncbi.nlm.nih.gov/22096103/" target="_blank" rel="noreferrer noopener">late Permian period</a>, serving as key plant chompers in ecosystems from South Africa to Russia. Their success ended abruptly when roughly 90 percent of marine species and 70 percent of land vertebrates vanished at the close of the era.



Yinshanosaurus angustus foraged on the northern shoulder of <a href="https://www.earth.com/news/forest-fossils-from-earths-largest-mass-extinction-carry-a-climate-warning/">Pangea</a>, the single landmass that stitched together today’s continents. 



At the time, the interior of the supercontinent swung between searing summers and bitter winters, pressuring animals to adapt or disappear.



China’s Naobaogou and Sunjiagou formations capture that turbulent landscape in stacked mudstones and siltstones. 



Periodic floods buried carcasses quickly enough to preserve delicate <a href="https://www.earth.com/news/scientists-discover-a-33-foot-jurassic-giant-twice-as-big-as-its-cousin-xingxiulong/">skeletal</a> links, a stroke of luck for modern paleontologists.



<h2 class="wp-block-heading" id="h-clues-written-in-bone">Clues written in bone</h2>



Yi and Liu spotted a forked rear projection on the nasal bone and a notch in the tabular bone at the back of the skull, features never seen together before. 



They also noticed a U‑shaped paraoccipital process that differs from the V‑shaped version in close cousins.



“The skeleton of Yinshanosaurus angustus provides the complete cranial and articulated postcranial details of Chinese pareiasaurs for the first time,” added Jian Yi after months of lab preparation. 



Using 183 anatomical characters, the team ran computer analyses that split Chinese pareiasaurs into three distinct branches, placing the new taxon beside <a href="https://dbpedia.org/page/Shihtienfenia" target="_blank" rel="noreferrer noopener">Shihtienfenia completus</a> within a fresh sub‑group.



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



The Permian ended with volcanic eruptions in what is now Siberia, pumping out enough carbon dioxide to warm oceans by at least 14°F. 



That spike drove <a href="https://www.earth.com/news/cascading-oxygen-loss-could-endanger-our-oceans/">ocean anoxia</a>, acid rain, and habitat collapse, setting the stage for the dinosaurs that would follow in the Triassic.



Each newly described pre‑extinction species sharpens models of how ecosystems responded to rising heat and disrupted carbon cycles. 



Because pareiasaurs sat low on the land food chain, they reflect the health of primary plant production more directly than predators do.



<h2 class="wp-block-heading" id="h-from-dig-site-to-digital-tree">From dig site to digital tree</h2>



CT scans of the Shanxi skull reveal replacement tooth buds waiting beneath worn crowns, confirming lifelong dental turnover like that in <a href="https://www.earth.com/news/fossil-discovery-shifts-the-origin-of-lizards-back-35-million-years/">modern lizards</a>. 



The scans also expose internal canals that once carried blood vessels to horn‑like bosses, suggesting seasonal growth tied to mating display or species recognition



Digital models of those structures feed into the expanding open database hosted by the Chinese Academy of Sciences. 



By pooling 3‑D files from separate labs, researchers can test competing family trees without moving fragile <a href="https://www.earth.com/news/what-fossils-tell-us-about-life-after-mass-extinction/">fossils</a> across borders.



<h2 class="wp-block-heading" id="h-yinshanosaurus-angustus-and-the-future">Yinshanosaurus angustus and the future</h2>



Work now shifts to beds just above the current fossil horizon, layers that may hold early <a href="https://www.earth.com/news/triassic-fossils-shed-new-light-on-ancient-ecosystems/" target="_blank" rel="noreferrer noopener">Triassic</a> survivors or fresh victims of the end‑Permian crisis. 



Liu’s group plans a targeted survey during the next field season, armed with drone‑based photogrammetry to map promising outcrops.



The team also hopes to sample bone collagen, if any remains, for stable‑isotope studies that could reveal diet and seasonal water stress. 



Combined with climate models, those data might show whether narrow‑snouted herbivores had a feeding edge in arid late Permian landscapes.



Understanding how a mid‑sized, flat‑snouted browser fit into the pre‑extinction puzzle helps scientists refine the timeline of faunal turnover. 



Each added piece, however small, tests broader ideas about resilience and collapse as Earth’s systems tip past critical thresholds.



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Yinshanosaurus angustus <a href="https://www.earth.com/wp-content/uploads/2025/07/Yinshanosaurus-angustus_tetraod_illustration_credit-Guo-IVPP_1m.jpg">image credit</a>: Guo, Institute of Vertebrate Paleontology and Paleoanthropology (IVPP)



The study is published in <a href="https://onlinelibrary.wiley.com/doi/10.1002/spp2.70020" target="_blank" rel="noreferrer noopener">Papers in Palaeontology</a>.



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Scientists discover a prehistoric animal that lived on Earth 259 million years ago

A new fossil skull, dug out of purple siltstone in...

Many expect warmer winters to reduce cold snaps, but that hasn’t happened. A new study reveals that what happens high in the stratosphere still controls much of what happens at ground level.



A swirling band of cold air, the stratospheric polar vortex (SPV), sometimes shifts or weakens. Two specific variations of this vortex send Arctic air plunging into the U.S. One pattern (called P2) leads to severe weather in the Northwest. 



The other (P3) hits the Central and Eastern regions. Since 2015, the Northwest has faced more of these brutal cold <a href="https://www.earth.com/news/astonishing-global-heat-in-january-2025-defied-climate-expectations/">events</a>, while the East has seen fewer. This shift aligns with more frequent La Niña episodes.



The study was conducted by researchers from the <a href="https://www.uml.edu" target="_blank" rel="noreferrer noopener">University of Massachusetts Lowell</a>, Hebrew University of Jerusalem, and the Massachusetts Institute of Technology.



“The public often hears about the ‘polar vortex’ when winter turns severe, but we wanted to dig deeper and understand how variations within this vortex affect where and when extreme cold hits,” said the researchers.



<h2 class="wp-block-heading" id="h-the-vortexes-that-drive-winter-cold">The vortexes that drive winter cold</h2>



Using four decades of data, the researchers clustered five recurring SPV shapes (P1 to P5). Two of them, P2 and P3, were most associated with U.S. cold outbreaks.



P2 features a strong vortex centered over the pole with a stretched lower vortex. It often brings snow and cold to the Northwestern U.S. 



P3 shows a weaker, displaced vortex toward the North Atlantic, steering cold into the Central and Eastern U.S. These variations do not just depend on vortex position but also on how atmospheric waves behave.



Planetary waves can either be absorbed or reflected in the stratosphere. When reflected, they can send cold air barreling southward. P3 events consistently show this reflection during the cold wave itself. P2 events often have wave reflection before the <a href="https://www.earth.com/news/climate-equation-predicts-a-rapid-rise-in-extreme-heatwaves/">cold</a> snap hits.



<h2 class="wp-block-heading" id="h-where-the-cold-hits-and-why">Where the cold hits and why</h2>



The researchers used the rAWSSI index, which considers temperature, snow depth, and snowfall.



The analysis revealed that P3 patterns produce the most extreme winter conditions in the Central and Eastern U.S., while P2 patterns primarily affect the Northwestern region with intense cold and snowfall. The findings help explain recent cold events, including the severe Texas freeze of 2021.



The Northwest has seen more P2 days recently. This increase matches a northwestward shift in cold air <a href="https://www.earth.com/news/global-warming-is-accelerating-beyond-control-as-co2-levels-rise/">outbreaks</a>. The central and eastern parts still get hit, but less often now.



Wave activity flux (WAF) offers clues. Before P2 events, reflection happens over Siberia and Alaska. During P3 events, strong reflection occurs over Asia and the Pacific. In P3, this reflection continues as the cold air descends.



Cold air starts in the east, spreads across the Midwest, and settles in the Northwest. These transitions help forecast where the next cold wave might land.



<h2 class="wp-block-heading" id="h-global-cycles-influence-winter-cold">Global cycles influence winter cold</h2>



P2 is more frequent during La Niña conditions. P3 prefers El Niño phases. This suggests tropical ocean <a href="https://www.earth.com/news/earth-is-on-pace-to-surpass-1-5c-global-temperature-increase-for-second-year-in-a-row/">temperatures</a> influence how the polar vortex behaves.



Other climate patterns play a role as well. The westerly phase of the Quasi-Biennial Oscillation (QBO) often coincides with P2 days. 



On the other hand, the Arctic Oscillation (AO) tends to be more negative during P3 events, a state that supports increased cold outbreaks in the Central and Eastern United States.



<h2 class="wp-block-heading" id="h-winter-cold-is-shifting">Winter cold is shifting</h2>



Despite a warming climate, these findings suggest extreme cold will still return. But its location may shift. In the past decade, the coldest anomalies moved westward. That’s a change from decades of more common Eastern U.S. cold.



With better tracking of SPV patterns, meteorologists can now look 2 to 4 weeks ahead. The study shows that P3 often precedes P2, which means that a Central or Eastern cold event may be followed by a Northwestern one.



The high-altitude stratosphere, once seen as distant and separate, plays an active role in shaping winter. As climate change accelerates, it’s no longer enough to track surface temperatures. We need to watch the sky, too.



The research was funded by the National Science Foundation (<a href="https://www.nsf.gov/" target="_blank" rel="noreferrer noopener">NSF</a>) , the U.S.–Israel Binational Science Foundation (<a href="https://www.bsf.org.il/" target="_blank" rel="noreferrer noopener">BSF</a>) , the U.S. Department of Energy (<a href="https://www.doe.gov/" target="_blank" rel="noreferrer noopener">DOE</a>) , and the National Oceanic and Atmospheric Administration (<a href="https://www.noaa.gov/" target="_blank" rel="noreferrer noopener">NOAA</a>).



The study is published in the journal <a href="https://www.science.org/doi/10.1126/sciadv.adq9557" target="_blank" rel="noreferrer noopener">Science Advances</a>.



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Why global warming hasn’t ended extreme winter cold

Many expect warmer winters to reduce cold snaps, but that...

Niagara Falls pulls in tourists by the boatload. Angel Falls towers higher than city skyscrapers. Yet both pale in comparison to Earth's largest waterfall - an enormous, rushing torrent concealed below Arctic waves.



The Denmark Strait cataract drops in slow motion beneath the chilly surface between Iceland and Greenland. 



The chute begins thousands of feet down, rolls over a hidden ledge, and keeps sliding for 11,500 feet - more than twice the cruising altitude of a commercial jet. 



No roar reaches the surface, no mist fills the air, and passing ships glide on as if nothing remarkable lies below these crucial <a href="https://www.earth.com/news/atlantic-and-arctic-mixing-is-crucial-for-earths-climate-stability/">Arctic waters</a>, which drive Earth's climate.



<h2 class="wp-block-heading" id="h-the-denmark-strait-cataract">The Denmark Strait cataract</h2>



Most of Earth's largest waterfalls form when a river meets a cliff and spills over. Turbulent water gouges the rock, the lip grows steeper, and a postcard scene is born. 



<a href="https://www.nature.com/articles/s41598-024-75984-z" target="_blank" rel="noreferrer noopener">Submarine waterfalls</a> follow a different script. Here, colder, saltier water sinks below lighter layers, slipping along the seafloor like syrup down a tilted pan. The motion is silent, pulling entire water masses rather than a single stream.



Oceanographers first confirmed the Denmark Strait cataract decades ago by tracing temperature and salinity profiles through the channel. 



Sensors revealed a dense ribbon of <a href="https://www.earth.com/news/arctic-ocean-stayed-partly-open-during-harsh-ice-ages/">Nordic Sea</a> water sliding into the Atlantic basin, gathering speed until it tumbled past a submerged ridge. That ridge acts as the unseen cliff, setting off the tallest plunge on Earth.



<h2 class="wp-block-heading" id="h-where-arctic-chill-meets-atlantic-warmth">Where Arctic chill meets Atlantic warmth</h2>



Icy water leaving the Nordic seas is both colder and saltier than the milder Atlantic layer to the south. Density differences created by that contrast drive the flow. 



As the dense water reaches the sill between <a href="https://www.earth.com/image/rare-glimpse-of-iceland-amid-unusual-heatwave/">Iceland</a> and <a href="https://www.earth.com/news/greenland-ice-fossil-tundra-discovery-stuns-and-worries-scientists-sea-level-rise/">Greenland</a>, it spills downward, widening as it falls until the sheet stretches roughly 300 miles - about the driving distance from Chicago to St. Louis.



During the <a href="https://www.earth.com/news/lessons-from-the-ice-age-how-climate-change-reshapes-plant-life/">Last Ice Age</a>, roughly 17,500 to 11,500 years ago, glaciers carved trenches across the seabed and left behind the ridge that now serves as the cataract’s tipping point. 



Glacial debris, <a href="https://www.earth.com/news/rocks-explain-roman-empire-collapse-1500-years-ago-late-antique-little-ice-age/">volcanic eruptions</a>, and relentless currents have since hardened the structure, locking a geological funnel in place for the descending water.



<h2 class="wp-block-heading" id="h-climate-change-and-the-largest-waterfall">Climate change and the largest waterfall</h2>



More than 3.2 million cubic meters of water - around 113 million cubic feet - slip over the cataract every second, far outpacing the Amazon River’s flow into the Atlantic. 



This slide feeds the lower limb of the Atlantic Meridional Overturning Circulation (<a href="https://www.nature.com/articles/s43247-025-02403-0" target="_blank" rel="noreferrer noopener">AMOC</a>), the global “conveyor belt” that ferries heat, oxygen, and nutrients around the planet.



There is increasing evidence of the effects of global change on the phenomenon of undersea waterfalls. 



“A good example is on the <a href="https://www.earth.com/image/the-ebro-river-on-the-northeast-coast-of-spain/">Catalan coast</a>, where the decrease in the number of tramontane days in winter in the Gulf of Lion and north of the Catalan coast is causing a weakening of this oceanographic process, which is decisive in regulating the climate and has a great impact on deep ecosystems,” explains marine scientist <a href="https://www.researchgate.net/profile/Anna-Sanchez-Vidal" target="_blank" rel="noreferrer noopener">Anna Sanchez Vidal</a>.



<h2 class="wp-block-heading" id="h-size-of-the-denmark-strait-cataract">Size of the Denmark Strait cataract</h2>



<a href="https://en.wikipedia.org/wiki/Angel_Falls" target="_blank" rel="noreferrer noopener">Angel Falls</a> drops 3,212 feet in Venezuela. Niagara clears a modest 167 feet on the U.S.-Canada border. Stack all of Niagara’s water several dozen times, and you still won’t match the cataract’s flow. 



Even the Mississippi at flood stage would struggle. Yet the Denmark Strait cataract remains invisible, its roar muffled by more than a half-mile of seawater.



Instruments tell a different story: moored profilers register velocities topping three knots, while sediment cores show layers rearranged by the hidden torrent.



The phenomenon of dense water overflow is particularly intense in the Arctic and Antarctic. 



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2024/12/denmark-strait-cataract_graphic-illustration_credit-NOAA_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2024/12/denmark-strait-cataract_graphic-illustration_credit-NOAA_1s.webp" alt="In the Denmark Strait, southward-flowing frigid water from the Nordic Seas meets warmer water from the Irminger Sea. The cold, dense water quickly sinks below the warmer water and flows over the huge drop in the ocean floor, creating a downward flow estimated over 123 million cubic feet per second. Credit: NOAA" class="wp-image-1977524"/></a><figcaption class="wp-element-caption">In the Denmark Strait, southward-flowing frigid water from the Nordic Seas meets warmer water from the Irminger Sea. The cold, dense water quickly sinks below the warmer water and flows over the huge drop in the ocean floor, creating a downward flow estimated over 123 million cubic feet per second. Click image to enlarge. Credit: NOAA</figcaption></figure>



“The poles are the regions where most of the dense water masses - generated by the formation of sea ice at the surface - eventually reach the global ocean floor," explains David Amblàs of the <a href="https://www.ub.edu/portal/web/earth-sciences/faculty" target="_blank" rel="noreferrer noopener">Department of Earth and Ocean Dynamics</a> at the University of Barcelona. 



"The polar areas are like the heart of the oceanic circulatory system: they pump cold, dense water into the great oceanic troughs through the ‘heartbeats’ made by overflows of dense water."



<h2 class="wp-block-heading" id="h-much-more-to-learn">Much more to learn</h2>



The cataract may slow or speed up as <a href="https://www.earth.com/news/drastic-warming-will-transform-the-arctic-beyond-recognition/">Arctic warming</a> alters salinity and temperature patterns. Researchers use autonomous gliders, deep-sea landers, and satellite altimetry to watch for any shift that could ripple through weather systems. 



A weakening flow might stall the North Atlantic’s heat pump, cooling Europe and nudging hurricanes onto new tracks.



Yet there is still no direct video of the full descent, and no sensor array captures every eddy. Each expedition peels back only a sliver of the story. 



Future projects aim to stitch those slivers together, mapping the plunge in three dimensions and tracking its pulse through the seasons.



<h2 class="wp-block-heading" id="h-why-earth-s-largest-waterfall-matters">Why Earth's largest waterfall matters</h2>



Anyone enjoying mild January weather or a fish fillet pulled from Icelandic waters owes thanks, in part, to the Denmark Strait cataract. 



By dragging cold, dense water southward, the cataract clears space for warmer <a href="https://www.earth.com/news/weakening-ocean-currents-could-cost-trillions-of-dollars/">Gulf Stream water</a> to flow north. That exchange tempers winter, nourishes plankton, and steers migratory species toward fertile feeding grounds.



When the torrent quickens, more carbon-rich deep water rises elsewhere, boosting ocean productivity. When it slackens, heat piles up in the tropics, whipping up stronger storms. 



In other words, the waterfall no one can see holds a backstage pass to everyday weather and the seafood aisle alike.



From a tourist’s point of view, the cataract offers nothing to watch. From a planetary perspective, it's a crucial lever, tilting climate and commerce with the quiet push of density-driven flow. 



Scientists will keep chasing its rhythm, because the better we know this hidden giant, the better we can forecast the moods of the sea and the sky above it.



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Earth’s largest waterfall, dwarfing all others, is hidden in the ocean

Niagara Falls pulls in tourists by the boatload. Angel Falls...

Abuse or neglect in the preschool years appears to push a child’s internal clock forward while also steering their eyes away from the very cues that build trust. 



Two separate biological and social signals - faster cellular aging and reduced eye contact - foreshadow later struggles with emotions and behavior.



The evidence comes from the <a href="https://www.ugscd-osaka-u.ne.jp/en/">United Graduate School of Child Development</a>, a consortium of several leading Japanese universities specializing in child development research.



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



Long-term studies already link childhood maltreatment to heart disease, <a href="https://www.earth.com/news/seven-healthy-lifestyle-habits-that-prevent-depression/">depression</a>, and premature death, yet pinpointing the earliest biological shifts has been tricky. 



Many investigations lean on teenagers’ memories or on broad stress hormones that rise for many reasons.



The Japanese team aimed lower in age and deeper in detail, asking what happens inside the body and in live social behavior before a child enters grade school.



<h2 class="wp-block-heading" id="h-clocking-childhood-stress-in-cells">Clocking childhood stress in cells</h2>



Ninety-six four- and five-year-olds visited the university lab with a caregiver they trusted. Thirty-six of them suffered confirmed severe childhood maltreatment; the remaining sixty formed a comparison group.



Technicians took a painless cheek swab and measured DNA methylation patterns with the Pediatric-Buccal-Epigenetic clock - a method this group refined in earlier work. 



The algorithm converts chemical tags on genes into an “epigenetic age.” If that number outruns the child’s actual age, researchers infer that wear and tear has set in early.



The abused children’s cells looked markedly older, even after the analysts adjusted for sex, birth weight, and household income. 



Accelerated <a href="https://www.earth.com/news/epigenetic-dna-clocks-predict-biological-age-more-accurately/">epigenetic clocks</a> in adults often foreshadow <a href="https://www.earth.com/news/new-type-of-diabetes-type-5-is-now-officially-recognized-linked-to-nutritional-deficiencies/">diabetes</a>, stroke, and early mortality. Spotting the same pattern in four-year-olds suggests damage is already under way while most of the brain is still wiring itself.



<h2 class="wp-block-heading" id="h-abused-children-miss-social-cues">Abused children miss social cues</h2>



Next came a social test. High-resolution eye-tracking cameras recorded exactly where and how long each child looked while short videos played.



When faces appeared on screen, youngsters with a history of abuse spent far less time examining the eye region than their peers.



<a href="https://www.earth.com/news/dog-and-human-brains-sync-up-during-eye-contact/">Eye contact</a> feeds children information about emotions, intentions, and safety. Avoiding it deprives them of a fast, intuitive map of other people’s feelings just when they are learning to navigate friendships.



<h2 class="wp-block-heading" id="h-abuse-disrupts-on-two-fronts">Abuse disrupts on two fronts</h2>



Statistical models showed that cellular aging and gaze avoidance each predicted higher scores on caregiver checklists of <a href="https://www.earth.com/news/gut-microbes-have-an-unexpected-link-to-anxiety/">anxiety</a>, aggression, and attention problems.



Yet the two did not sit in a single chain. Faster clocks did not explain why eyes wandered, and wandering eyes did not explain the faster clocks. Trauma, it seems, injures children along at least two independent tracks.



“Our research sends a powerful message: child maltreatment can leave invisible but measurable marks on a child’s biology and social development. By identifying these early warning signs, we can step in earlier and provide targeted support,” said lead author Keiko Ochiai.



“Tools such as eye-tracking assessments and stress-related biological testing could help teachers, doctors, and caregivers expedite the identification of children at risk,” she added.



“Support programs can then be tailored to improve social skills, reduce emotional stress, and promote healthier development - potentially preventing more serious problems later in life.”



<h2 class="wp-block-heading" id="h-catching-childhood-maltreatment-early">Catching childhood maltreatment early</h2>



Because the study captured a single snapshot in time, it cannot prove that abuse causes every change.



Poverty, prenatal stress, or inherited risks may also accelerate epigenetic clocks or nudge eyes away from faces. Even so, the data place the first measurable cracks astonishingly early, suggesting that age four is not too soon - perhaps not even soon enough - to intervene.



Crucially, both assessments are simple to bring into clinics and preschools. Cheek swabs require no needles, and modern processors can read methylation signatures in hours. Portable eye trackers now fit on a laptop.



Embedding these tools into routine checkups could flag vulnerable youngsters before <a href="https://www.earth.com/news/stress-hijacks-the-brain-disrupting-sleep-and-memory/">stress</a> cements into chronic disease or social isolation.



<h2 class="wp-block-heading" id="h-helping-young-people-reset-the-clock">Helping young people reset the clock</h2>



The researchers have already begun a follow-up that will revisit the same children in middle school to see whether early cellular age predicts adolescent depression, metabolic illness, or continued social withdrawal.



They also hope to test whether nurturing foster care, trauma-focused therapy, or parent-training programs can slow the epigenetic clock and coax eyes back to faces.



Childhood is meant to stretch time, not compress it. Yet when abuse or neglect crowds those years with fear, the body and mind appear to leap forward, aging faster and dodging the very gaze that could bring comfort.



Detecting those hidden signals of childhood maltreatment offers a rare chance to reset the clock and guide young people toward a future where curiosity, connection, and health unfold at the pace nature intended.



The study is published in the journal <a href="https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0321952">PLOS One</a>.



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Childhood maltreatment speeds up aging and alters behavior

Abuse or neglect in the preschool years appears to push...

As oceans heat up, coastal sharks are adjusting their calendars. Instead of swimming south in early fall, many are now sticking around longer due to global warming. 



Researchers at <a href="https://www.stonybrook.edu" target="_blank" rel="noreferrer noopener">Stony Brook University</a> tracked this trend by following six shark species along the U.S. East Coast. They used acoustic tags and detection models to uncover how ocean warming delays the sharks’ southern migrations by up to 29 days.



"Both temperature and photoperiod (length of sunlight) influenced the timing of the <a href="https://www.earth.com/news/greenland-sharks-survive-for-centuries-in-icy-waters/">sharks</a>’ southernly migration, and it is likely that they both cumulatively influence migratory patterns,” said lead author Maria Manz.



<h2 class="wp-block-heading" id="h-sharks-delay-migration-due-to-warming">Sharks delay migration due to warming</h2>



The study observed blacktip, dusky, sand tiger, sandbar, thresher, and white <a href="https://www.earth.com/news/how-the-sharks-body-grows-with-geometric-precision/">sharks</a>. Among them, sandbar sharks showed the longest delay of up to 29 days. They also used the widest range of latitudinal zones, from the New England Shelf to Florida.



White sharks, by contrast, showed the least delay. Being partially warm-bodied (regional endotherms), they are less dependent on external temperature shifts. Their migration changed by only one day under future climate scenarios.



<h2 class="wp-block-heading" id="h-east-coast-is-warming-fast">East Coast is warming fast</h2>



The study focused on the Mid-Atlantic Bight. This region, especially the New York Bight and New England Shelf, is heating faster than many other parts of the Atlantic. 



According to projections based on the high-emissions SSP5 8.5 scenario, the New England Shelf could warm by over 2°C (3.6°F) by 2049.



This rise in temperature affects not just the water, but everything in it. Fish prey species may move earlier or later, altering food availability for predators like sharks.



“Results of the models suggested that projected increases in SST across decades may delay southern autumn <a href="https://www.earth.com/news/rare-video-footage-of-an-elusive-deep-sea-predator-pacific-sleeper-shark/">migrations</a> of coastal sharks with many species remaining in northern habitats for longer durations," wrote the researchers.



<h2 class="wp-block-heading" id="h-how-sharks-were-tracked-in-warming-waters">How sharks were tracked in warming waters</h2>



The researchers tagged 155 sharks and monitored their movements using over 390 acoustic receivers. These receivers picked up signals from the tags whenever sharks came within 900 meters (2,953 feet).



The sharks’ migrations were tracked across five defined zones: New England Shelf (NES), New York Bight (NYB), Mid-Atlantic (MA), Southern Atlantic (SA) and Florida (FL).



Some species, like sandbar and thresher sharks, appeared in all zones. Others, like white sharks, showed more restricted ranges.



<h2 class="wp-block-heading" id="h-predictors-of-migration-timing">Predictors of migration timing</h2>



To understand what drives sharks to migrate, the researchers fed their data into mixed-effect Cox models. 



The team tested sea surface temperature (SST), photoperiod, and lunar phase. Photoperiod emerged as a consistently strong predictor, especially for thresher <a href="https://www.earth.com/news/shark-skeletons-could-lead-to-technological-innovations/">sharks</a>.



Interestingly, lunar phase had less influence than expected. Only sandbar sharks showed some sensitivity to moonlight patterns. 



Most migration timing was better explained by combinations of light and temperature, which can vary regionally.



<h2 class="wp-block-heading" id="h-warming-delays-and-shark-survival">Warming delays and shark survival</h2>



If sharks delay migration but human activities continue on schedule, it could spell trouble. For example, commercial fishing in the Northeast typically ramps up in the fall. Sharks that remain in the area face a higher risk of accidental catch.



“Our findings suggest that climate change could increase vulnerability to bycatch, particularly in mixed-use areas like the New York Bight,” the authors wrote.



There is also concern that shark diets and reproductive cycles may shift out of sync with prey availability. A mismatch in timing could reduce feeding success or breeding success.



<h2 class="wp-block-heading" id="h-new-strategies-for-a-changing-ocean">New strategies for a changing ocean</h2>



Static conservation policies will not hold up if shark behavior keeps changing. The researchers suggest dynamic management tools, like adjusting fishery closures based on temperature data.



Sandbar sharks, which showed the most migration delay, may require special focus. They are already listed as vulnerable due to previous overfishing and slow reproduction.



Successful conservation now depends on real-time data and predictive modeling. As this study shows, changes in migration are not hypothetical. They are already underway.



<h2 class="wp-block-heading" id="h-shark-migration-is-shifting-with-warming">Shark migration is shifting with warming</h2>



The timing of shark migrations is shifting. Some species are adapting by staying longer in warming northern waters. While that may suit them for now, it raises questions about long-term ecological impacts.



Maria Manz and her team stress the importance of using both regional climate data and shark movement models. Doing so can improve predictions and help managers adjust strategies before the ocean changes even more.



"Our study adds to the growing body of evidence demonstrating how migratory populations will respond to a warming climate, potentially altering regional ecosystem dynamics and exposure to anthropogenic threats."



The research is published in the journal <a href="https://conbio.onlinelibrary.wiley.com/doi/10.1111/cobi.70080" target="_blank" rel="noreferrer noopener">Conservation Biology</a>.



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Warming oceans are changing shark migration patterns

As oceans heat up, coastal sharks are adjusting their calendars....

Our galaxy may be wrapped in a richer swarm of tiny companions than astronomers have ever seen. New calculations predict that there are dozens of ultra-faint satellite galaxies circling close to the Milky Way.



They are too dim for current surveys to spot, but real enough to tip the cosmic balance sheet in favor of standard cosmology.



The forecast comes from cosmologists at <a href="https://www.durham.ac.uk/">Durham University</a>. By combining the sharpest supercomputer simulations available with new mathematical modeling, the team argues that up to 100 additional satellites should be lurking nearby.



Many are likely to be “orphan” galaxies, almost entirely stripped of the dark matter cocoons that once cradled them. This twist could finally resolve a long-standing mismatch between theory and observation.



<h2 class="wp-block-heading" id="h-the-milky-way-s-ghost-galaxies">The Milky Way’s ghost galaxies</h2>



The study begins with the Lambda Cold Dark Matter framework. In this model, roughly five percent of the cosmos is ordinary matter, twenty-five percent is cold <a href="https://www.earth.com/news/study-dark-matter-does-not-exist-and-the-universe-is-27-billion-years-old/">dark matter,</a> and the remaining seventy percent is dark energy.



In this model, galaxies shine from the centers of vast dark-matter halos. Most star systems in the Universe are low-mass dwarf galaxies bound to a more massive host.



The problem is that classic LCDM computations generate far more dwarf satellites than astronomers have cataloged around the Milky Way. Either the model is wrong or the satellites are missing.



To probe that gap, the Durham group turned to the <a href="https://www.eso.org/public/videos/aquarius_springel/">Aquarius simulation</a>, the highest-resolution model yet of a Milky Way-like dark-matter halo. The team also used <a href="https://galaxies.northwestern.edu/">GALFORM</a>, a code that tracks gas cooling, <a href="https://www.earth.com/news/fluffy-molecular-clouds-may-change-our-understanding-of-star-formation/">star formation</a>, and feedback.



Even top tools miss tiny halos when they near the galaxy and feel its tidal pull. Analytical fixes revived erased halos, letting researchers track their stellar remnants across 13 billion years.



<h2 class="wp-block-heading" id="h-lost-galaxies-cluster-nearby">Lost galaxies cluster nearby</h2>



The key insight is that the galaxies whose halos entered the Milky Way’s neighborhood early have spent eons being stretched, prodded, and shaved by gravity. Their dark matter bleeds away first; their stars shrink into faint knots that simulations often drop but nature should keep.



The models suggest that these ghostly remnants have orbital histories similar to the brighter satellites we already know. They tend to cluster within a few hundred thousand light-years of the galactic center.



Because they are faint and sparse, current imaging misses them, but the <a href="https://www.earth.com/news/first-images-from-the-vera-c-rubin-observatory-are-breathtaking/">Vera C. Rubin Observatory</a>’s LSST camera, now undergoing commissioning, should pull many into view.



“We know the Milky Way has some 60 confirmed companion satellite galaxies," said lead author Isabel Santos-Santos, a cosmologist at Durham. "We think there should be dozens more of these faint galaxies orbiting around the Milky Way at close distances.” 



If their predictions are correct, it strengthens support for the Lambda Cold Dark Matter theory of how structure in the Universe forms and evolves.



“Observational astronomers are using our predictions as a benchmark with which to compare the new data they are obtaining,” she said. “One day soon, we may be able to see these ’missing’ galaxies, which would be hugely exciting and could tell us more about how the Universe came to be as we see it today.”



<h2 class="wp-block-heading" id="h-future-images-of-the-milky-way">Future images of the Milky Way</h2>



Over the past decade, wide-field cameras such as the <a href="https://www.darkenergysurvey.org/">Dark Energy Survey</a> have turned up about thirty ultra-faint satellite candidates. 



Yet astronomers still debate whether these specks are true dwarf galaxies embedded in dark matter or merely star-cluster outliers.



The study argues that many of them - and many more beyond - should indeed be galaxies, the visible tips of dark-matter fragments pared to the bone. 



Future deep imaging and stellar-population studies will be critical for deciding which candidates carry dark matter signatures such as elevated velocity dispersions.



<h2 class="wp-block-heading" id="h-finding-the-milky-way-s-ghost-galaxies">Finding the Milky Way's ghost galaxies</h2>



“If the population of very faint satellites that we are predicting is discovered with new data, it would be a remarkable success of the LCDM theory of galaxy formation,” said co-author Carlos Frenk, a professor of computational cosmology at Durham.



"Using the laws of physics, solved using a large supercomputer, and mathematical modelling we can make precise predictions that astronomers, equipped with new, powerful telescopes, can test."



Validating the prediction would also quiet doubts raised by the so-called “missing satellite” and “too-big-to-fail” problems - tensions often cited as cracks in LCDM.



If the Milky Way does host scores of nearly invisible ghost galaxies, then the theory’s tally of dark-matter clumps stands. What looked like a failure of physics may be a failure of detection.



<h2 class="wp-block-heading" id="h-ghosts-become-neighbors">Ghosts become neighbors</h2>



With LSST set to map the southern skies to unprecedented depths, the hunt for hidden satellites is gaining momentum. Other instruments, such as the European Space Agency’s Euclid telescope, will help sharpen the picture. 



New algorithms tuned to pick out diffuse, low-surface-brightness objects will scan the LSST deluge, guided by the locations and properties the Durham models predict.



Discovering even a fraction of the proposed “orphan” galaxies would give cosmologists a richer lab for testing how dark matter behaves on small scales and how starlight survives in extreme environments.



It would also remind us that the Milky Way, though serene to the naked eye, belongs to a teeming, fragile community of companions.



For now, they remain ghosts in a computer. But new telescopes may soon reveal them as real, stellar neighbors, deepening our understanding of how galaxies, large and small, take shape in the dark.



The research was presented at the <a href="https://conference.astro.dur.ac.uk/event/7/">National Astronomy Meeting of the Royal Astronomical Society</a>.



Image Credit: The Aquarius simulation, the Virgo Consortium/Dr. Mark Lovell



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Dozens of 'ghost galaxies' may be orbiting the Milky Way

Our galaxy may be wrapped in a richer swarm of...

Stray sandstone and quartz pebbles strewn across a quiet beach near Breiðavík, Iceland, look innocuous, yet they hold evidence of a climate shock that chilled Europe nearly 1,500 years ago and jolted the late Roman world.



New microscopic work on those stones shows they were ferried from Greenland by icebergs during the onset of the <a href="https://www.sciencedirect.com/science/article/pii/S2095927322004790" target="_blank" rel="noreferrer noopener">Late Antique</a> Little Ice Age - a cold spell lasting two‑to‑three‑centuries that followed a string of giant volcanic eruptions.



<h2 class="wp-block-heading" id="h-volcanoes-bring-a-little-ice-age">Volcanoes bring a Little Ice Age</h2>



<a href="https://www.earth.com/news/tree-rings-show-amazon-rainfall-is-getting-more-extreme/">Tree‑ring</a>, <a href="https://www.earth.com/news/greenland-ice-fossil-discovery-stuns-and-worries-scientists/" target="_blank" rel="noreferrer noopener">ice‑core</a>, and historical data point to eruptions in 536, 540, and 547 AD that injected so much sulfate into the stratosphere that summer temperatures dropped by up to 3 °F across the Northern Hemisphere, setting the stage for years of failed harvests.&nbsp;



Climatologists later labeled this interval the Late Antique Little Ice Age, as mentioned above, noting that North Atlantic summers stayed cool from about 536 to 660 AD. 



This finding was backed by a 2016 multi‑proxy reconstruction of Eurasian temperatures. 



<h2 class="wp-block-heading" id="h-studying-iceland-beaches">Studying Iceland beaches</h2>



During field mapping on Iceland’s west coast, Spencer’s group spotted cobbles made of granite, gneiss, and even serpentinite embedded within otherwise basaltic beach terraces.



“We knew these rocks seemed somewhat out of place because the rock types are unlike anything found in <a href="https://www.earth.com/image/rare-glimpse-of-iceland-amid-unusual-heatwave/">Iceland today</a>, but we didn’t know where they came from,” said <a href="https://www.queensu.ca/geol/dr-christopher-spencer-phd-pgeo" target="_blank" rel="noreferrer noopener">Christopher Spencer</a> of Queen’s University.



Samples came from a low terrace about 6 feet above today’s high‑tide line, a bench that earlier work had dated to the seventh century. 



The team reasoned that the terrace formed as land rebounded after the last <a href="https://www.earth.com/news/current-climate-goals-arent-enough-to-stop-massive-glacier-losses/">glaciers</a> from the Little Ice Age melted, meaning any exotic stones trapped there arrived by sea rather than human hands.



<h2 class="wp-block-heading" id="h-little-ice-age-and-zircon-analysis">Little Ice Age and zircon analysis</h2>



Back in the lab, researchers crushed each cobble and sifted out specks of zircon, a hardy mineral that preserves its birthplace like a fingerprint.



<a href="https://www.sciencedirect.com/topics/earth-and-planetary-sciences/zircon-u-pb-dating" target="_blank" rel="noreferrer noopener">U‑Pb dating</a> showed age clusters at roughly 2.8, 1.15, 0.5, and 0.24 billion years, a combination that matches crustal provinces across <a href="https://pubs.geoscienceworld.org/gsa/geology/article/doi/10.1130/G53168.1/653479/Greenlandic-debris-in-Iceland-likely-tied-to-Bond" target="_blank" rel="noreferrer noopener">Greenland</a> but not Iceland, firmly tying the pebbles to the other side of the Denmark Strait.



“[This is] the first direct evidence of icebergs carrying large Greenlandic cobbles to Iceland,” Spencer noted. 



Grain size and rounding indicate that the rocks traveled inside floating ice rather than as loose sand, so the voyage probably lasted weeks or months before the bergs melted on Icelandic shores.



The team also measured hafnium isotopes inside the same zircons, yielding chemical signatures unique to Greenland’s <a href="https://www.frontiersin.org/journals/earth-science/articles/10.3389/feart.2020.540997/full" target="_blank" rel="noreferrer noopener">North Atlantic craton</a>, a confirmation that rules out Icelandic sources and signals a voyage of roughly 800 miles.



<h2 class="wp-block-heading" id="h-iceberg-highways-in-the-little-ice-age">Iceberg highways in the Little Ice Age</h2>



Ocean‑current reconstructions suggest that a stronger <a href="https://www.britannica.com/science/subpolar-gyre" target="_blank" rel="noreferrer noopener">Subpolar Gyre</a> during the sixth century shepherded bergs toward Iceland, while cooler seas slowed melting and extended travel times. 



Modeling shows that a 1 °F drop in summer sea‑surface temperature lengthens the iceberg‑survival zone by almost 200 miles, allowing debris to drift far beyond normal limits.



Geologists link the seventh‑century spike in ice‑rafted debris to Bond event 1, a recognizable pulse of iceberg discharge recorded in North Atlantic sediment cores that sits squarely within the sixth‑century cooling interval.



The Icelandic cobbles add a shoreline data point to that marine signal and confirm that extra ice once clogged the Denmark Strait.



<h2 class="wp-block-heading" id="h-climate-shock-for-rome">Climate shock for Rome</h2>



During the Late Antique Little Ice Age, <a href="https://www.earth.com/news/volcanic-gold-precious-metals-discovered-hawaii-may-have-come-from-earths-core/">volcanic</a> aerosol veils dimmed sunlight, shortened growing seasons, and helped trigger a famine that struck the Eastern Mediterranean in the 540s, the same decade the Justinian Plague swept through Constantinople.



“When it comes to the fall of the Roman Empire, this climate shift may have been the straw that broke the camel’s back,” explained <a href="https://www.southampton.ac.uk/people/5x7llb/professor-thomas-gernon" target="_blank" rel="noreferrer noopener">Tom Gernon</a> of the University of Southampton.



Historians such as <a href="https://history.fas.harvard.edu/people/michael-mccormick" target="_blank" rel="noreferrer noopener">Michael McCormick</a> point to tax records showing lower grain shipments from Egypt to Rome after 536 AD, evidence that the breadbasket of the empire faltered just as Germanic kingdoms pressed south.



Tree‑ring reconstructions reveal that alpine summers during 536-660 AD were the coldest of the past two millennia, supporting the view that climatic stress compounded existing political fractures.



<h2 class="wp-block-heading" id="h-feedback-loops-and-the-roman-empire">Feedback loops and the Roman Empire</h2>



Cooler summers curbed cereal yields, livestock weights, and tax revenue, weakening imperial logistics. Hun and Gothic groups seeking pasture migrated toward warmer latitudes, colliding with <a href="https://www.earth.com/news/lead-pollution-may-have-caused-the-fall-of-the-roman-empire/">Roman</a> frontiers and accelerating military overstretch.



In turn, warfare destroyed irrigation and trade networks, deepening famine and amplifying disease spread, a vicious cycle typical of complex systems under environmental stress. 



That shock arrived on top of plague and revenue crises, stacking stressors in a way familiar to modern analysts who study compound disasters.



Modern shipping lanes now dominate the <a href="https://www.earth.com/news/earths-largest-waterfall-is-hidden-in-the-ocean/">Denmark Strait</a>, yet satellite data still capture plumes of drift ice after large eruptions, a reminder that the ocean-ice engine remains active.



Understanding ancient episodes like the Late Antique Little Ice Age helps planners anticipate how future volcanic winters or polar meltwater pulses could ripple through food, trade, and migration networks today.



-----



The research team behind the discovery includes scientists from <a href="https://www.queensu.ca/" target="_blank" rel="noreferrer noopener">Queen’s University</a>, the <a href="https://www.southampton.ac.uk/" target="_blank" rel="noreferrer noopener">University of Southampton</a>, and the <a href="https://english.cas.cn/" target="_blank" rel="noreferrer noopener">Chinese Academy of Sciences</a>.



The study is published in <a href="https://pubs.geoscienceworld.org/gsa/geology/article-abstract/53/7/572/653479/Greenlandic-debris-in-Iceland-likely-tied-to-Bond?redirectedFrom=fulltext" target="_blank" rel="noreferrer noopener">Geology</a>.



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Scientists discovered rocks that explain the fall of the Roman Empire 1,500 years ago

Stray sandstone and quartz pebbles strewn across a quiet beach...

Even a brief jab from a pin or the sting of a hot pan can leave behind pain that lingers as dread, worry, and distress. Researchers have now pinpointed a strand of nerve cells that splice those emotions onto raw sensation. 



The research was conducted at the <a href="https://www.salk.edu/">Salk Institute for Biological Studies</a>, where neuroscientist Sung Han and his colleagues mapped this pathway in mice. The findings show how a spinal spark becomes both a sharp twinge and a wave of misery.



By isolating calcitonin gene-related peptide (CGRP) neurons in a small pocket of the thalamus and tracing their links to the <a href="https://www.earth.com/news/lizard-brain-shapes-social-abilities-in-humans/">amygdala</a>, the team made a key discovery. They showed that this branch of the classic spinothalamic tract carries the feelings that make pain matter.



<h2 class="wp-block-heading" id="h-the-emotional-triggers-of-pain">The emotional triggers of pain</h2>



For decades, the prevailing view was that the brain processes sensory and emotion-related aspects of pain through separate pathways.



“But there’s been debate about whether the sensory pain pathway might also contribute to the emotional side of pain," Han said. "Our study provides strong evidence that a branch of the sensory pain pathway directly mediates the affective experience of pain.”



In other words, the same “highway” that delivers information about heat or pressure can fork into lanes that deliver pain feelings.



<h2 class="wp-block-heading" id="h-rewriting-the-pain-textbook"><a></a>Rewriting the pain textbook</h2>



Textbooks have long split pain in two. Fast sensory signals climb the spinothalamic tract to the thalamus. From there, they travel to the sensory cortex, letting you spot where you were burned and how hot it was.



A second route - the spinoparabrachial tract - was said to feed emotion and shock to the brainstem.



The Salk findings blur that distinction. By injecting tracers into the spinal cords of mice, the team followed some spinothalamic fibers to the parvocellular subparafascicular nucleus of the thalamus. 



This region is home to CGRP-tagged neurons that wire straight to the amygdala, the hub for <a href="https://www.earth.com/news/fear-and-anxiety-the-mental-health-impacts-of-wildfires/">fear and anxiety</a>.



<h2 class="wp-block-heading" id="h-turning-emotion-on-and-off">Turning emotion on and off</h2>



To test what the cells do, researchers genetically silenced the CGRP neurons. Mice still withdrew from a hot plate or pinprick, proving that sensory detection was intact. However, they stopped avoiding places where that discomfort had occurred.



When the same neurons were flicked on with light-driven optogenetics, the animals avoided the chamber even though no pain stimulus was present, a sign of pure emotional distress.



“Pain processing is not just about nerves detecting pain; it’s about the brain deciding how much that pain matters,” said first author Sukjae Kang.



“Understanding the biology behind these two distinct processes will help us find treatments for the kinds of pain that don’t respond to traditional drugs.”



<h2 class="wp-block-heading" id="h-pain-beyond-the-wound">Pain beyond the wound</h2>



Many difficult disorders - fibromyalgia, <a href="https://www.earth.com/news/mysteries-of-migraines-explained-by-brain-fluid-dynamics/">migraine</a>, and some forms of post-traumatic stress - feature overwhelming pain or threat without obvious tissue injury.



Gene expression analysis showed that thalamic CGRP neurons carry several signatures already linked to migraine. Drugs that block CGRP are already easing migraine attacks in clinics.



Han’s team suggests these drugs could calm the thalamic circuit that turns everyday bumps and sounds into agony.



“Our discovery of the CGRP affective pain pathway gives us a molecular and circuit-level explanation for the difference between detecting physical pain and suffering from it,” Han said. 



“We’re excited to continue exploring this pathway and enabling future therapies that can reduce this suffering.”



<h2 class="wp-block-heading" id="h-making-pain-more-treatable">Making pain more treatable</h2>



Everyone feels the initial jab at roughly the same stimulus strength, yet people vary wildly in how long they brood over it. The new work shows that variation may begin inside the thalamus, not only in higher thought centers.



By revealing a precise set of neurons that add the emotion behind the pain, the study opens the door to therapies that dull suffering without muting essential warning signals.



Clinicians could one day pair CGRP blockers with behavioral therapy to restore a balanced response to hurt.



<h2 class="wp-block-heading" id="h-looking-beyond-physical-hurt">Looking beyond physical hurt</h2>



The Salk team now plans to trace the same circuit in other species and to test whether it reacts to social pain such as heartbreak or <a href="https://www.earth.com/news/animal-grief-may-look-nothing-like-human-sorrow/">grief</a>.



If the CGRP loop proves to be a general “alarm” network, dialing it down might help people whose brains stay locked in high alert after trauma.



For the millions living with chronic pain, the discovery offers concrete hope that scientists can uncouple sensation from suffering. It could let a simple bruise heal without haunting the mind.



The study is published in the journal <a href="https://www.pnas.org/doi/10.1073/pnas.2505889122">Proceedings of the National Academy of Sciences</a>.



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Why pain feels emotional: New brain pathway linked to suffering

Even a brief jab from a pin or the sting...

Rainforests thrive on delicate relationships. Plants, animals, and insects like ants constantly interact, creating a web of survival and competition. Amid this chaos, unexpected harmony sometimes blooms.



In the tropical rainforests of Fiji, scientists uncovered a fascinating story of peacekeeping. It is not a tale of advanced creatures or complex brains. Instead, it centers around a plant with an unusual design. 



This plant has developed a surprisingly simple strategy to solve conflict among aggressive ants.



This discovery from <a href="https://www.durham.ac.uk" target="_blank" rel="noreferrer noopener">Durham University</a> reshapes our understanding of cooperation in <a href="https://www.earth.com/news/how-future-climate-conditions-will-transform-plant-growth/">nature</a>. It shows how something as basic as plant architecture can manage aggression and encourage mutual support. 



The study reveals that, sometimes, structure itself can shape behavior and nurture harmony among rivals.



<h2 class="wp-block-heading" id="h-ants-and-plants-team-up">Ants and plants team up</h2>



The plant at the center of this story belongs to the genus Squamellaria. It is part of the Rubiaceae family, also known as the coffee family. These plants grow on the branches and trunks of rainforest trees.



The plants form large, bulbous structures called domatia. These domatia are not just growths - they serve as homes for ants. In return for shelter, ants provide the <a href="https://www.earth.com/news/scientists-finally-learn-what-makes-plants-roots-grow-faster-and-stronger-autophagy/">plant</a> with essential nutrients from their waste.



However, the ants that live in these plants are not naturally friendly neighbors. Many of them are highly aggressive and often engage in violent fights with other species. 



This raises an important question: how can so many aggressive species coexist peacefully inside a single plant?



<h2 class="wp-block-heading" id="h-walls-keep-rivals-apart">Walls keep rivals apart</h2>



The answer lies in the design of Squamellaria’s domatia. Professor Guillaume Chomicki of Durham University led an international team to investigate the mystery. 



Using high-resolution 3D CT scans, the researchers explored the inner structure of the plant’s domatia. What they found was remarkable. The plant creates domatia with multiple chambers, each completely sealed off from the others inside.



Every chamber has its own entrance, but inside, walls separate them from their neighbors. This design prevents physical contact between ant <a href="https://www.earth.com/news/plant-roots-could-be-key-to-fighting-climate-change/">species</a>. It is as if the plant built a miniature apartment complex, with each species living in its own secure unit.



This clever separation prevents fights and keeps the peace within the plant. It is not a chemical trick or behavioral adaptation by the ants. The plant’s architecture itself enforces harmony.



<h2 class="wp-block-heading" id="h-one-plant-many-ants">One plant, many ants</h2>



To test the effectiveness of this system, the researchers conducted extensive fieldwork. They observed Squamellaria plants on three Fijian islands for over a decade.



The team's observations revealed that a single Squamellaria <a href="https://www.earth.com/news/plants-could-soon-talk-to-farmers-and-listen-too/">plant</a> could house as many as five different ant species simultaneously. Despite their natural tendency to fight, the ants coexisted peacefully.



The researchers also performed nutrient labeling experiments using nitrogen isotopes. These experiments confirmed that all of the ant species provided valuable nutrients to the plant. 



Each ant colony contributed to the plant’s well-being, making the relationship mutually beneficial for all involved.



<h2 class="wp-block-heading" id="h-when-peace-breaks-down">When peace breaks down</h2>



To truly understand the importance of separation, the researchers conducted a bold experiment. They surgically removed the internal walls between the chambers of the domatia.



The results were immediate and violent. Ant species that had previously lived peacefully erupted into fierce battles. These fights led to many ant deaths on both sides.



In contrast, plants with intact chambers saw no such conflict. Even outside the plant, ants shared food sources without issue. This highlights the importance of physical separation inside the plant.



“It is incredible how such an odd group of organisms, restricted to a couple of <a href="https://www.earth.com/news/nasa-warning-sea-level-rise-in-pacific-island-nations-is-irreversible/">Fijian islands</a>, can provide general insights into the stability of cooperation between species,” noted Professor Chomicki.



<h2 class="wp-block-heading" id="h-a-plant-that-solves-conflicts">A plant that solves conflicts</h2>



The team also created mathematical models to further explore the plant’s strategy. The models confirmed that compartmentalization helps maintain long-term partnerships. 



The system prevents fights during the early stages of colony establishment. This allows each chamber to develop into a stable, nutrient-contributing <a href="https://www.earth.com/news/just-a-few-ants-can-change-an-entire-colonys-social-structure/">colony</a>.



Even in situations where only a small fraction of arriving ants were aggressive, the models showed that compartmentalized domatia performed better than single-chambered ones.



This shows that separating rivals is not just a short-term solution. It has lasting benefits for both the plant and its ant residents. The architecture ensures that mutualism remains stable over time, providing security and resources for all involved.



<h2 class="wp-block-heading" id="h-hidden-harmony-in-nature">Hidden harmony in nature</h2>



This discovery helps solve a long-standing mystery in ecology. Scientists have wondered how unrelated and sometimes hostile species manage to maintain cooperation.



The findings suggest that physical separation could be a widely used strategy in nature. Many organisms may rely on similar methods to prevent conflict and maintain beneficial relationships.



The study of Squamellaria shows that architecture alone can shape ecosystems. It highlights the hidden power of structural design in keeping peace among species that would otherwise be at odds.



In the rainforests of Fiji, a simple plant demonstrates that sometimes, the best way to manage conflict is to keep your neighbors at a safe distance.



The study is published in the journal <a href="https://www.science.org/doi/10.1126/science.adu8429" target="_blank" rel="noreferrer noopener">Science</a>.



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Some plants have a strategy to prevent violent ant fights

Rainforests thrive on delicate relationships. Plants, animals, and insects like...

A patch of grass, a shady tree, or a sandbox just beyond the front door can nudge children toward stronger self-control years later. New evidence ties tiny slivers of nature at home to key thinking skills in preschoolers, suggesting that everyday greenery does more than lift spirits.



Researchers at the <a href="https://illinois.edu/">University of Illinois Urbana-Champaign</a> followed Midwestern families from infancy to kindergarten as part of the <a href="https://www.familyresiliency.illinois.edu/strong-kids-2-cells-society-approach-nutrition">STRONG Kids2 project</a>. 



By merging satellite mapping with parent surveys, postdoctoral scholar Samantha Iwinski and colleagues tested how backyard features and family routines interact to build - or blunt - executive function (EF) in <a href="https://www.earth.com/news/genes-influence-blood-pressure-from-early-childhood/">early childhood</a>.



<h2 class="wp-block-heading" id="h-green-space-and-child-self-control">Green space and child self-control</h2>



Executive function is the mental toolbox that helps youngsters remember rules, switch focus, and curb impulses. Scientists separate it into “cold” skills, such as paying <a href="https://www.earth.com/news/our-brain-stops-paying-attention-to-repeated-distractions/">attention</a> and planning, and “hot” skills, which manage <a href="https://www.earth.com/news/brainwaves-reveal-that-positive-emotions-enhance-memory/">emotions</a>. The Illinois team asked whether nearby outdoor elements would tilt the scales.



“We looked at what people have outside their home or across the street, where they can just walk out their door, and we focused on children’s access to these facilities before age two,” Iwinski said.



“The goal was to investigate how those environmental factors shaped children’s cognitive abilities as well as the home environment, because it's all part of a holistic system of influences.”



Google Earth images pinpointed trees, lawns, sandboxes, decks, and outdoor storage at 435 households spanning apartments, single-family homes, and farms. 



Annual home visits then measured toddlers’ executive skills and gauged household order - or chaos - through questions on noise, routines, and crowding.



<h2 class="wp-block-heading" id="h-sandbox-time-builds-child-focus">Sandbox time builds child focus</h2>



Iwinski and her team found that having trees, a sandbox, or outdoor storage space before age 2 was linked to stronger cold executive function by age four.



“Trees and a sandbox allow for sensory interaction and are part of a natural playscape, providing opportunities to touch and feel and potentially climb," she said. "Outdoor storage space could mean there are toys and games that promote outdoor activities.”



Children who could reach such features showed greater ability to concentrate and follow directions when tested two years later.



Other landscape cues favored “hot” executive function. “This could relate to socializing and connection. <a href="https://www.earth.com/news/birth-of-farming-driven-by-humans/">Farming</a> communities are often close-knit. Having a deck provides an opportunity to sit together and talk,” Iwinski noted.



Preschoolers raised on farms or with a porch to gather on were better at calming themselves when upset and delaying gratification at ages four and five.



<h2 class="wp-block-heading" id="h-greener-yards-calmer-homes"><a></a>Greener yards, calmer homes</h2>



Families surrounded by lush vegetation also reported less household chaos - fewer sudden noises, more predictable schedules, and less overall stress. 



Parents seemed to use outside time as a pressure valve, turning shared walks or sandbox play into moments of restoration for adults and kids alike.



Still, the story was not one-directional. High chaos at ages two and four hurt executive skills in those same years, yet the pattern flipped later on.



“But we found that higher household chaos at earlier time points actually resulted in better EF at 4 years of age," Iwinski said. This could be because children develop resilience and adaptability, learning to regulate themselves in a chaotic environment.”



The finding hints that some turbulence, if paired with supportive caregiving, may teach flexibility.



<h2 class="wp-block-heading" id="h-green-space-gap-persists-for-children">Green space gap persists for children</h2>



The team warns that access is uneven. Research shows that children in low-income families have the most nature deprivation. 



"It would be important to implement policies that help underserved communities to have more <a href="https://www.earth.com/news/urban-green-spaces-are-urgently-needed-across-the-global-south/">green space</a> and ways to interact available, and to ensure everyone feels welcome and safe in outdoor environments,” Iwinski said.



Pocket parks, community gardens, and traffic-calmed streets could provide small pockets of green space for children where private yards are scarce.



<h2 class="wp-block-heading" id="h-make-nature-part-of-play">Make nature part of play</h2>



Tiny habit shifts may help families harvest cognitive benefits even before policy catches up. 



“Parents can talk about what to do, for example, ‘we can play with rocks today, tomorrow we can do sand,’ and show their kids what it means to be outside,” Iwinski said.



“It’s not just about helping your child, but also yourself, because outdoor activities promote mental health and restoration for everyone.”



Educators can extend the lesson by dotting school grounds with raised beds or movable log slices. Even a short recess under a tree canopy may sharpen attention back in the classroom.



<h2 class="wp-block-heading" id="h-nature-shapes-growing-minds">Nature shapes growing minds</h2>



The study knits together <a href="https://www.earth.com/news/landscapes-with-a-mix-of-habitats-are-biodiversity-hotspots/">landscape design</a>, family psychology, and child development into a single storyline: nature near home can quiet the household, invite unstructured exploration, and prime young brains for the twin tasks of focus and emotion control. 



It also shows that the benefits accrue well before children learn to read or add, highlighting a critical window for urban planners and caregivers alike.



Future work will track the same cohort into middle childhood to see whether early green space exposure predicts academic success or social adjustment.



For now, the message is simple and actionable: add a tree, keep a bucket of sand, or set out chairs on the porch - then step outside and play. The mind that steadies itself amid swaying branches or gritty fingers may carry that balance for years to come.



 The study is published in the journal <a href="https://muse.jhu.edu/article/959179">Children, Youth and Environments</a>.



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Green spaces have a major impact on child development

A patch of grass, a shady tree, or a sandbox...

Happy,Young,Mother,Bonding,With,Her,Toddler,Son,In,Blue

Singing to a baby may feel like nothing more than a timeless tradition, yet fresh data now proves just how much those soft tunes matter. Researchers at <a href="https://www.yale.edu/" target="_blank" rel="noreferrer noopener">Yale University</a> ran a four‑week experiment and saw babies’ mood ratings climb when parents were nudged to sing more often.



<h2 class="wp-block-heading" id="h-lullaby-benefits">Lullaby benefits</h2>



Parents have always trusted songs to soothe, and science backs that trust. In a 2021 <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220405/" target="_blank" rel="noreferrer noopener">study</a>, infants’ heart rates and skin conductance dropped when they heard lullabies in foreign languages. 



Those calming effects appear stronger than speech alone, hinting that melody taps regulatory circuits <a href="https://www.earth.com/news/social-dancing-and-singing-lullabies-to-babies-are-not-innate-human-behaviors/">beyond ordinary talk</a>.



Another experiment showed that seven‑ to ten‑month‑olds listened to singing for about twice as long as speech before fussing. 



Taken together, these findings explain why even sleep‑deprived caregivers keep humming when nothing else works.



<h2 class="wp-block-heading" id="h-cultural-roots-of-singing-to-babies">Cultural roots of singing to babies</h2>



Across time and geography, parents have sung to soothe, bond, and signal safety. 



<a href="https://www.ethnomusicology.org/" target="_blank" rel="noreferrer noopener">Ethnomusicology</a> studies show that infant-directed singing has distinct features, like slower tempo, repetitive structure, and pitch exaggeration, that appear in nearly every society’s lullabies. 



These songs aren't just tradition. They likely emerged because they work. In communities without formal parenting tools or gadgets, music acts as an instinctive caregiving method that bridges generations, languages, and lifestyles. 



Understanding this <a href="https://www.earth.com/news/music-causes-similar-emotional-experiences-and-sensations-in-all-cultures/">global pattern</a> helps explain why singing continues to be a reliable tool in modern households, regardless of background.



<h2 class="wp-block-heading" id="h-finding-out-if-singing-helps-babies">Finding out if singing helps babies</h2>



<a href="https://www.eunchomusic.com/about-me">Eun Cho</a> of the <a href="https://www.eunchomusic.com/about-me" target="_blank" rel="noreferrer noopener">Yale Child Study Center</a> and colleagues recruited 110 families with babies younger than four months. 



Using ecological momentary assessment, a smartphone survey method that pings parents randomly through the day, they captured real‑time mood snapshots instead of relying on memory.



Half the parents got karaoke‑style videos, songbooks, and weekly prompts; the rest continued usual care. 



Within a week most in the music group were singing in nearly nine out of ten survey windows, and that habit stuck after the prompts stopped.



“Parents intuitively gravitate toward music as a tool for managing infants' emotions, because they quickly learn how effective singing is at calming a fussy baby,” said <a href="https://psychology.fas.harvard.edu/people/samuel-mehr" target="_blank" rel="noreferrer noopener">Samuel Mehr</a>, director of <a href="https://www.themusiclab.org/" target="_blank" rel="noreferrer noopener">The Music Lab</a>. 



Parents were never told when to sing, yet they instinctively reached for music during bouts of fussing. 



Survey data confirmed his point: singing became the only soothing technique that rose significantly during the intervention. Babies whose caregivers sang more showed higher overall mood scores, not just momentary relief.



<h2 class="wp-block-heading" id="h-why-music-reaches-the-infant-brain">Why music reaches the infant brain</h2>



<a href="https://www.earth.com/news/similar-patterns-music-language-found-across-all-cultures/">Cross‑cultural work</a> finds songs tied to infant care in every documented society, suggesting an evolutionary role. 



Melodies carry repetitive rhythms and exaggerated pitch contours that match babies’ sensitivity to temporal patterns.



These <a href="https://www.earth.com/news/babies-hear-far-more-speech-at-home-than-music/">acoustic cues</a> likely signal safety, driving a physiological downshift: slower heart rate, calmer nervous system, steadier gaze. 



Because the same core features appear in many musical traditions, even unfamiliar songs can have the desired effect.



<h2 class="wp-block-heading" id="h-singing-helps-both-babies-and-parents">Singing helps both babies and parents</h2>



While the Yale trial did not boost caregiver mood in four weeks, other work hints at downstream benefits. 



A 10‑week group‑singing program in Italy eased <a href="https://www.frontiersin.org/journals/medicine/articles/10.3389/fmed.2024.1461965/full" target="_blank" rel="noreferrer noopener">postpartum depression</a> symptoms and was rated feasible for public clinics.



Lower infant distress can also lighten parental stress loads, improving sleep and bonding over time. Researchers plan longer studies to test whether daily singing shifts family health more broadly.



<h2 class="wp-block-heading" id="h-homes-without-music">Homes without music?</h2>



While many families in the Yale study already used music daily, not all households have the same habits. Earlier <a href="https://www.sciencedirect.com/science/article/pii/S0163638324000079" target="_blank" rel="noreferrer noopener">research</a> using all‑day audio recorders found surprisingly little music in many infants’ environments, even when parents assumed they sang often.



This gap means some babies may miss out on the emotional support <a href="https://www.earth.com/news/mothers-can-use-singing-to-engage-with-infants/">singing</a> provides, especially in homes facing stress, poverty, or limited caregiver time. 



Low‑cost tools like the ones used in the study, songbooks, videos, simple reminders, may help close that gap and give all babies the same access to mood‑lifting interaction. 



Even a small boost in daily musical moments could be a game‑changer for the most vulnerable infants.



<h2 class="wp-block-heading" id="h-bringing-music-home">Bringing music home</h2>



No special skill, speaker, or playlist is required. Pick any simple tune, nursery rhyme, folk song, or a chorus you like, and <a href="https://www.earth.com/news/finding-their-voice-how-singing-empowers-children/">sing</a> it at diaper changes, before naps, or in the evening bath. 



Keep the tempo slow, the volume soft, and repeat phrases so your baby learns the pattern. 



Consistency, not perfection, appears to be what a newborn brain craves, and caregivers already hold the most responsive instrument.



Your voice is enough. And for your baby, it might just be the best sound in the world. The science agrees: a few songs a day can go a long way.



The study is published in <a href="https://srcd.onlinelibrary.wiley.com/doi/10.1111/cdev.14246" target="_blank" rel="noreferrer noopener">Child Development</a>.



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Singing to babies significantly improves their mood and overall well-being, study confirms

Singing to a baby may feel like nothing more than...

Central Asia is running faster than nature can keep up. The latest region‑wide audit shows that human claims on land, water, and ecosystem productivity have blown past levels scientists call safe.



The research was led by Professor Duan Weili of the <a href="http://english.egi.cas.cn/" target="_blank" rel="noreferrer noopener">Chinese Academy of Sciences</a> and post‑doctoral researcher Zhu Ziyang. Together with an international team, they tracked six environmental <a href="https://www.earth.com/news/world-water-day-2025-preserving-glaciers-protecting-our-future/">footprints</a> from 2000 to 2020.



<h2 class="wp-block-heading" id="h-asia-s-rising-water-crisis">Asia’s rising water crisis</h2>



Across the five republics the land footprint already triples the share allowed under the down‑scaled <a href="https://www.stockholmresilience.org/research/planetary-boundaries.html" target="_blank" rel="noreferrer noopener">planetary boundaries</a>. Meanwhile, the metric known as <a href="https://wad.jrc.ec.europa.eu/humanappropriation" target="_blank" rel="noreferrer noopener">human appropriation of net primary production</a> climbs even higher. 



Kazakhstan and Uzbekistan are the two biggest borrowers from nature, earning a “priority management” label in the study for their outsized ecological withdrawals.



The <a href="https://www.earth.com/news/new-discovery-water-molecules-will-force-chemistry-textbooks-to-be-rewritten/">pattern</a> is lopsided in another way: more than 80 percent of every footprint originates inside the region, so trade alone cannot solve the crunch. 



Researchers link the spike to rapid population growth and a construction boom fueled by fossil fuel revenues. They also point to an agricultural model inherited from Soviet central planning.



<h2 class="wp-block-heading" id="h-land-use-threatens-wildlife-and-soil">Land use threatens wildlife and soil</h2>



Converting pasture and desert fringe into irrigated farms strips wild vegetation of the carbon it once fixed and fragments habitats needed by pollinators and large herbivores. 



By 2020, Tajikistan’s sustainability ratio for land‑based productivity had climbed above 90 - a level ecologists regard as ecological emergency territory.



Heavy harvesting of photosynthetic energy thins the soil. Downstream, dust storms take over, carrying eroded silt hundreds of miles into parched <a href="https://www.earth.com/news/earths-land-based-water-storage-has-drastically-diminished-and-its-not-being-replaced/">basins</a>. Biodiversity follows the same downward slope, squeezing ancient steppe communities that evolved with far lighter grazing pressure.



<h2 class="wp-block-heading" id="h-asia-s-old-farming-wastes-water">Asia’s old farming wastes water</h2>



Irrigated farming absorbs roughly 90 percent of diverted water, and aging Soviet‑era canals leak about 40 percent of that volume before it ever reaches a field. 



Cotton, the historic export staple, drinks more than twice as much water per pound of lint as winter wheat, further draining the Amu Darya and Syr Darya rivers of Central Asia.



Field trials in the Fergana Valley show that drip lines trimmed water use by 18-42 percent while boosting <a href="https://www.researchgate.net/publication/222181065_Water_use_efficiency_of_irrigated_cotton_in_Uzbekistan_under_drip_and_furrow_irrigation" target="_blank" rel="noreferrer noopener">irrigation efficiency</a> by up to 103 percent. 



Yet only a sliver of cropland currently benefits from such technology, largely because farmers lack capital and clear water‑pricing <a href="https://www.earth.com/news/water-might-have-formed-long-before-galaxies/">signals</a>.



<h2 class="wp-block-heading" id="h-pollution-from-farming-and-factories-nbsp">Pollution from farming and factories&nbsp;</h2>



Greenhouse‑gas <a href="https://longreads.cabar.asia/climatechangecentralasia_en" target="_blank" rel="noreferrer noopener">inventories</a> put the region’s annual emissions near 470 million metric tons of CO2‑equivalent, roughly one percent of the global load. 



Nitrogen fertilizer use has increased alongside emissions, adding 628 million kilograms of reactive nitrogen over two decades. This surge has fueled algal blooms that clog irrigation gates.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/central-asia_climate-change_illustration_credit-Earths-Future_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/central-asia_climate-change_illustration_credit-Earths-Future_1s.webp" alt="Schematic diagram of the main components of human appropriation of net primary production in arid Central Asia. Credit: Earth's Future (2025)" class="wp-image-1977470"/></a><figcaption class="wp-element-caption">Schematic diagram of the main components of human appropriation of net primary production in arid Central Asia. Click image to enlarge. Credit: Earth's Future (2025)</figcaption></figure>



Domestic energy burning, petrochemical refining, and steel production together dominate the carbon tally, leaving little room for expansion without efficiency gains.



Because phosphorus runoff is smaller but more concentrated, it acts as a chronic pulse that degrades reservoir water quality. It also shortens canal life through biofouling.



<h2 class="wp-block-heading" id="h-asia-s-farming-can-save-water">Asia’s farming can save water</h2>



Uzbekistan’s gradual pivot from cotton to wheat and fruit since 2010 has already slowed land‑footprint growth, offering a glimpse of how crop diversification pays ecological dividends. 



Livestock policy is another lever; rotational <a href="https://thescipub.com/abstract/ojbsci.2025.209.218" target="_blank" rel="noreferrer noopener">t</a>r<a href="https://thescipub.com/abstract/ojbsci.2025.209.218" target="_blank" rel="noreferrer noopener">ials</a> in northern Kazakhstan improved pasture biomass and soil organic matter within three seasons, even under heavy stocking rates.



Integrated crop-livestock systems recycle manure locally, cutting both chemical fertilizer demand and methane emissions from open lagoons.



 Precision seeding and deficit‑irrigation scheduling, common in U.S. Southwest farming, could translate readily to the warm, dry climate zones of the Kazakh steppe and the Karshi plain.



<h2 class="wp-block-heading" id="h-simple-solutions-can-save-nature">Simple solutions can save nature</h2>



“Our study shows that Central Asia's environmental pressure mainly stems from its domestic consumption," said study lead author Zhu Ziyang. "That calls for policies like better irrigation and scientific land management to bring development back inside a safe space.”



Canal lining, pressurized pipe networks, and solar‑powered pump retrofits each deliver quick water savings that postpone contentious upstream‑downstream negotiations.



On rangelands, subsidies that reward seasonal rests or herd rotation cost less than reseeding bare hillsides once degradation sets in. 



International lenders have begun to take notice. In May 2025, the World Bank approved a $200 million credit to modernize Uzbekistan’s irrigation and drainage grid. Disbursements are tied to measurable reductions in leaks.



<h2 class="wp-block-heading" id="h-asia-s-future-depends-on-water">Asia’s future depends on water</h2>



Scientists warn that six of nine planetary guardrails are already breached worldwide, so the region’s overshoot lands on a planet with shrinking shared headroom. 



Achieving absolute environmental <a href="https://www.earth.com/news/scientists-urgent-plea-sustainable-climate-solutions-save-earth-humanity/">sustainability</a> will demand that Central Asia cap resource use even as its population edges toward 45 million and summers grow hotter and drier.



How the five republics respond will shape whether future generations inherit a livable, functioning landscape. Their response will determine whether scarce resources are stabilized or continue to unravel under rising demand and outdated systems.



The study is published in the journal <a href="https://agupubs.onlinelibrary.wiley.com/doi/10.1029/2025EF006129" target="_blank" rel="noreferrer noopener">Earth's Future</a>.



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Central Asia has surpassed climate safety limits and now faces 'extreme unsustainability'

Central Asia is running faster than nature can keep up....

It’s easy to assume that when fish hang still in the water, they’re taking a break. After all, they look motionless - just calmly suspended in place. But new research shows that this “hovering” is actually a demanding task that takes more effort than resting.



The study comes from scientists at the University of California San Diego’s <a href="https://scripps.ucsd.edu/">Scripps Institution of Oceanography</a>. It focused on how fish manage to stay still in open water without sinking or drifting away.



The team found that fish burn nearly twice as much energy while hovering as they do when resting on the tank floor. That means what looks like rest is really anything but.



<h2 class="wp-block-heading" id="h-rethinking-stillness-in-fish">Rethinking stillness in fish</h2>



Most bony fish have swim bladders - gas-filled sacs that help them stay neutrally buoyant, which make them neither float upward nor sink. 



Because of this, researchers once thought that hovering was easy. But the new findings challenge that idea.



The scientists studied 13 different <a href="https://www.earth.com/news/small-fish-species-are-the-big-catch-of-the-future/">fish species</a> with swim bladders. Each fish was placed in a special tank where its oxygen use was recorded during two behaviors: resting on the bottom and hovering midwater. 



At the same time, high-speed cameras captured every fin twitch and tail flick.



The team also measured body features like the shape of the fish and the position of its <a href="https://www.earth.com/news/fins-and-limbs-share-a-deep-evolutionary-history/">fins</a>. One key measurement was the distance between the fish’s center of mass and center of buoyancy. 



These don’t always align. That small misalignment creates instability, which the fish must constantly correct.



“Hovering is a bit like trying to balance on a bicycle that’s not moving,” said Valentina Di Santo, an assistant professor at UC San Diego and study author.



<h2 class="wp-block-heading" id="h-stability-drains-fish-energy">Stability drains fish energy</h2>



Because of the mismatch between mass and buoyancy, hovering fish have to work against the natural tendency to roll, tilt, or drift. 



The more misaligned those centers are, the more energy the fish burns trying to stay still. That constant effort means hovering is far from restful.



“What struck me was how superbly all these fishes maintain a stable posture, despite their intrinsic instability,” said Di Santo.



Fish with more compact, deeper bodies like goldfish or pufferfish were better at hovering efficiently. In contrast, longer, thinner fish - like giant danios or shell dwellers - had to work harder. 



Fin position also played a role. Fish with pectoral fins placed farther back on their bodies generally hovered more efficiently. The researchers believe this may be due to improved leverage.



<h2 class="wp-block-heading" id="h-goldfish-have-an-edge">Goldfish have an edge</h2>



“This changes how we see hovering. It’s not a form of rest at all,” said Di Santo. “It’s an energetically costly activity but one that fish engage in anyway because it can be very useful.”



Fish may hover when guarding a nest, feeding in a specific spot, or holding their place in fast-moving water. These tasks require them to stay stable in one position, even when it’s exhausting. 



The study also pointed out a trade-off. Fish with shapes that give them greater control and agility often burn more energy while hovering. Meanwhile, more stable shapes are less agile.



But that trade-off may be worth it. Being able to move nimbly through coral reefs or complex underwater environments is key to survival.



<h2 class="wp-block-heading" id="h-fish-inspire-robot-design">Fish inspire robot design</h2>



The findings could also influence the next generation of underwater vehicles. Most robots today are built to be stable. But like fish, that stability may limit their agility.



“By studying how fish achieve this balance, we can gain powerful design principles for building more efficient, responsive underwater technologies,” said Di Santo.



For engineers, this could mean building in a bit of instability and designing systems that, like fins, actively correct for it. 



Doing so could allow underwater robots to better explore tight or cluttered environments, such as coral reefs or wreck sites.



“If you want a robot that can maneuver through tight spaces, you might have to learn from these fishes to design in some instability and then add systems that can dynamically maintain stability when needed,” said Di Santo.



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Fish don’t rest while hovering - it's actually hard work

It’s easy to assume that when fish hang still in...

Bees have long been admired for their delicate beauty and essential role in pollination. These small creatures, however, face growing challenges from their environment. 



Rising temperatures and pollution continue to reshape bee behavior in unexpected ways. Recent research is unveiling surprising links between environmental changes and the subtle buzzes bees produce.



These quiet vibrations are more than just background noise. They hold deep meaning for the survival of <a href="https://www.earth.com/news/world-bee-day-2025-protecting-the-pollinators-that-feed-the-world/">bees</a> and the ecosystems they support. As environmental pressures increase, understanding these sounds becomes even more important. 



Researchers are now focusing on how changes in temperature and exposure to heavy metals affect these essential vibrations. The findings offer insight into the hidden world of bee communication and pollination.



<h2 class="wp-block-heading" id="h-hidden-power-of-bee-muscles">Hidden power of bee muscles</h2>



Bees are renowned for their efficient flight. Their wings beat rapidly, allowing them to hover and move gracefully between flowers. However, not many know that <a href="https://www.earth.com/news/honey-bee-invasion-a-growing-threat-to-native-pollinators/">bees</a> also use their flight muscles for other important tasks.



“People have been long interested in how insect flight muscles work, as these muscles power the most efficient flight systems in nature,” said Dr. Charlie Woodrow, a post-doctoral researcher at <a href="https://www.uu.se/en" target="_blank" rel="noreferrer noopener">Uppsala University</a>. “However, many do not know that bees use these muscles for functions other than flight.”



These non-flight muscle vibrations help in several key behaviors. Bees use them for communication within the hive, to ward off threats, and during a special kind of pollination known as buzz pollination.



<h2 class="wp-block-heading" id="h-bees-buzz-flowers-to-collect-pollen">Bees buzz flowers to collect pollen</h2>



Buzz pollination stands out as one of the most fascinating <a href="https://www.earth.com/news/how-bumble-bees-are-sabotaging-their-own-health/">behaviors</a> in the insect world. It is a process where bees vibrate their bodies to dislodge pollen from certain types of flowers.



“Buzz pollination is an incredible behavior whereby a bee will curl its body around the pollen-concealing anthers of some flowers, and contract the flight muscles up to 400 times per second to produce vibrations which shake the pollen loose,” said Dr. Woodrow.



This act requires great energy and precision. The buzzing shakes the flower at exactly the right frequency, releasing the trapped pollen. 



Dr. Woodrow and his team aim to understand how these vibrations vary between species and environmental conditions. They hope to uncover how these differences affect pollination success and bee behavior.



<h2 class="wp-block-heading" id="h-tools-to-study-bee-buzzing">Tools to study bee buzzing</h2>



To explore these mysteries, Dr. Woodrow’s team turned to advanced technology. They studied buff-tailed bumblebees (Bombus terrestris), a common species found across Europe. These bees are ideal subjects because they are well-researched and easily handled.



Using accelerometers, the researchers measured the frequency of <a href="https://www.earth.com/news/organic-farms-and-meadows-can-help-save-wild-bees/">buzzing</a>. This frequency corresponds to the pitch of the sound we can hear.



“They are super easy to use in the field,” said Dr. Woodrow. “We press these against the thorax of the bee, or against the flower the bee is visiting, and we can record the vibrations the bee produces.”



<h2 class="wp-block-heading" id="h-how-bees-handle-buzzing-heat">How bees handle buzzing heat</h2>



Beyond vibration measurements, the team also used thermal imaging to understand how bees manage heat during buzzing. This approach allowed them to observe how bees balance their body temperature while performing demanding tasks.



“We have also been using high-speed filming to uncover never before seen behaviors,” said Dr. Woodrow. “For example, we recently discovered that bees don’t just vibrate on flowers, but they periodically transmit these vibrations to flowers by biting.”



These unexpected discoveries reveal how much remains hidden in the world of bees. They also highlight the importance of studying these creatures in detail, especially as the climate warms.



<h2 class="wp-block-heading" id="h-hidden-role-of-temperature">Hidden role of temperature</h2>



One of the most surprising findings from Dr. Woodrow’s research involves temperature. His experiments showed that temperature has a much stronger impact on buzzing than scientists had previously realised.



“We have recently found that temperature plays a vital role, much more than was previously appreciated, and this work is currently in review for publication,” said Dr. Woodrow. 



“This has many implications for how we study buzz-pollination, as temperature is not really something that has been considered up to this point.”



This insight could reshape how pollination research is conducted in the future, as temperature clearly affects buzzing behavior.



<h2 class="wp-block-heading" id="h-pollution-changes-bee-buzzing">Pollution changes bee buzzing</h2>



In addition to temperature, pollution also affects bee vibrations. Dr. Woodrow teamed up with Dr. Sarah Scott from <a href="https://www.ncl.ac.uk" target="_blank" rel="noreferrer noopener">Newcastle University</a> to investigate how heavy metals influence buzzing.



The experiments showed that heavy metal exposure reduces buzzing frequency during non-flight activities. 



Surprisingly, when the researchers tested bees in Arctic regions compared to those further south, they found no difference in the temperature’s effects on buzzing.



This suggests that internal muscle physiology may govern buzzing traits more than local adaptation does.



<h2 class="wp-block-heading" id="h-a-new-way-to-monitor-bee-health">A new way to monitor bee health</h2>



The research offers exciting possibilities beyond academic study. Understanding how environmental changes alter buzzing can reveal much about bee health and behavior. This knowledge can also improve technology designed to detect bee species using sound.



“Perhaps buzzes could even be used as a marker of stress or environmental change,” said Dr. Woodrow. “For example, we now know that certain environmental pollutants can affect the buzzes bees produce, so they could even serve as an indicator of ecosystem health.”



Monitoring bee buzzes could help identify species at risk and provide early warnings about environmental threats.



<h2 class="wp-block-heading" id="h-buzzing-changes-may-harm-bees">Buzzing changes may harm bees</h2>



The potential risks from disrupted buzzing extend beyond bees. Dr. Woodrow points out that changes in buzzing could damage several aspects of bee life.



“It is important we understand how these changes will affect non-flight buzzes because they are responsible for so many aspects of a bee’s ecology,” said Dr. Woodrow. 



“If these vibrations are disrupted, this could lead to poor communication in the colony, inefficient thermoregulation, or poor resource acquisition for their offspring.”



This disruption could limit pollination, affecting plant reproduction and biodiversity.



<h2 class="wp-block-heading" id="h-rising-heat-may-shift-bee-behavior">Rising heat may shift bee behavior</h2>



One particularly worrying result relates to the combination of high temperatures and energy costs.



“For example, buzz-pollination is energetically expensive and causes the bee to generate metabolic heat - therefore if the environment gets too warm, it may simply choose to avoid buzz-pollinated flowers,” noted Dr. Woodrow.



This behavioral change could weaken entire ecosystems, as many plants rely on bees for pollination. If bees avoid these plants, pollination rates could drop sharply.



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



While these findings raise concerns, they also point toward future innovation. Dr. Woodrow’s team is working on applying their research to robotics.



“We are working towards understanding bee vibrations through micro-robotics, so our results are also going towards developing micro-robots to understand pollen release,” said Dr. Woodrow.



This cross-disciplinary work may someday help protect pollination services by mimicking bee buzzing with machines.



<h2 class="wp-block-heading" id="h-urgent-need-to-protect-pollinators">Urgent need to protect pollinators</h2>



These discoveries will be shared at the <a href="https://www.sebiology.org" target="_blank" rel="noreferrer noopener">Society for Experimental Biology Annual Conference</a> in Antwerp, Belgium, on July 8, 2025. 



The findings show that bees face increasing challenges from environmental shifts, but they also present new tools to help understand and protect them.



As temperatures climb and pollutants spread, paying attention to the quiet buzz of bees could become more important than ever. Their tiny vibrations may hold the key to preserving plant life, biodiversity, and our shared future.



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Heat and pollution are changing the buzz of bees

Bees have long been admired for their delicate beauty and...

Koalas are everywhere on postcards and souvenirs. People think of them as calm animals sleeping in trees. But life isn’t simple for koalas anymore.



Their numbers keep dropping across Australia. Habitat loss, disease, and land clearing cause serious damage. Many forests are now small patches surrounded by roads and buildings.



Most people don’t realize how risky it is for <a href="https://www.earth.com/news/koalas-face-critical-threats-from-disease-and-habitat-loss/">koalas</a> when they leave trees. New research now shows something alarming. Koalas spend only about ten minutes a day on the ground, but those short minutes cause almost two-thirds of all recorded koala deaths.



<h2 class="wp-block-heading" id="h-koalas-risk-lives-when-leaving-trees">Koalas risk lives when leaving trees</h2>



Gabriella Sparkes, a PhD student at the <a href="https://www.uq.edu.au" target="_blank" rel="noreferrer noopener">University of Queensland</a>, wanted to gain a better understanding of koala behavior.



“Koalas are mostly tree-dwelling, but due to extensive land clearing, they’re increasingly forced to travel on the ground, which puts them at serious risk of injury and death,” said Sparkes. “I wanted to better understand what koalas do during these ground movements.”



Vehicles and dogs kill most <a href="https://www.earth.com/news/koalas-can-predict-hot-days-and-adjust-their-body-temperature/">koalas</a> while they walk on the ground. Even though this danger is known, many details about their movements remained unknown.



“We don’t yet have a clear understanding of how often koalas come down from trees, how far or fast they move, how long they stay on the ground, or what influences those decisions,” noted Sparkes. 



“These are critical knowledge gaps if we want to identify high-risk areas or times and develop strategies to reduce threats during these vulnerable moments.”



<h2 class="wp-block-heading" id="h-tracking-koalas-in-their-habitats">Tracking koalas in their habitats</h2>



Sparkes and her team used special collars on <a href="https://www.earth.com/news/world-wildlife-day-2025-a-global-call-to-protect-nature/">wild</a> koalas. These collars had GPS trackers and sensors called accelerometers.



The GPS recorded their locations every five minutes. When koalas started walking on the ground, the system switched to record every five seconds. 



The sensors measured their movements in detail. They showed if a koala was walking, sitting, or climbing.



“When paired with GPS tracks, this gives us an incredibly detailed view of how koalas move through their habitat,” said Sparkes.



<h2 class="wp-block-heading" id="h-koalas-prefer-staying-in-trees">Koalas prefer staying in trees </h2>



The results were clear. Koalas prefer staying in trees. They sleep, eat, and rest there most of the time. The researchers were surprised by how rarely koalas use the ground.



“What surprised us was how infrequently and briefly they use the ground—just 2-3 times per night, averaging around 10 minutes in total, or less than 1% of their day,” says Ms. Sparkes.



Koalas only climb down when they need to move between trees. But when trees are far apart, ground travel becomes unavoidable.



<h2 class="wp-block-heading" id="h-koalas-move-slowly-between-trees">Koalas move slowly between trees</h2>



People often think <a href="https://www.earth.com/news/un-report-disturbing-details-about-the-state-of-earths-wildlife/">animals</a> move quickly when they’re in danger. But this research showed that koalas don’t rush. They move slowly and pause often. They spend almost as much time sitting as they do walking.



“They spent nearly as much time sitting and pausing as they did walking, and only about 7% of their time on the ground was spent bounding,” said Sparkes. 



“This may indicate that koalas are carefully assessing their environment as they move, possibly evaluating trees before selecting one to climb, or it may reflect the energetic costs of bounding.”



Koalas may need to check for safety before climbing a tree. They might also avoid fast movements to save energy.



<h2 class="wp-block-heading" id="h-ways-to-keep-koalas-safe">Ways to keep koalas safe</h2>



This study, which was the first to track fine details of ground movement in wild koalas, has revealed clear risks and raised more questions. Sparkes and her team now study what makes koalas stay longer in trees.



“We’re now looking at environmental features that influence how long koalas stay in trees,” said Sparkes. 



“If we can identify the kinds of trees or habitat conditions that encourage koalas to remain in trees for longer, we may be able to design or manage landscapes in ways that reduce the need for ground travel.”



The goal is to find trees that keep koalas off the ground. The researchers also wanted to see if certain habitats lower the need for risky movements.



<h2 class="wp-block-heading" id="h-small-changes-can-help-koalas-survive">Small changes can help koalas survive</h2>



The team hopes their research can guide better conservation work. They suggest keeping tree canopies connected and reducing the space between trees.



Simple actions like planting the right trees may help. Koalas need safer, connected habitats to avoid ground travel.



“This research is just one piece of the puzzle, but it adds an important layer to our understanding of how koalas interact with increasingly human-altered environments,” said Sparkes.



The findings will be presented at the <a href="https://www.sebiology.org/">Society for Experimental Biology</a> Annual Conference in Antwerp, Belgium, in July.



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Most koalas don’t survive after leaving the safety of trees

Koalas are everywhere on postcards and souvenirs. People think of...

Anyone who has ever stopped on a busy street because a cluster of strangers were gazing at the sky knows how contagious attention can be. Humans aren’t the only species drawn into looking where others look.



A new study has shown that pigeons also track the gaze of their flockmates. The number of birds already looking determines how strongly the behavior spreads.



The research was led by Fumihiro Kano and Mathilde Delacoux at the <a href="https://www.uni-konstanz.de/en/">University of Konstanz</a>.



<h2 class="wp-block-heading" id="h-social-cues-guide-attention">Social cues guide attention</h2>



“Many animals, including humans, tend to look where others are looking. This is called gaze following,” said Delacoux. “It’s a simple but important way of sharing attention and learning from others.”



In the 1960s, social psychologist Stanley Milgram famously demonstrated what he called the “quorum effect” in people. If only one or two individuals stare at a building’s roof, most passers-by ignore them. But as the crowd of sky-watchers grows, almost everyone stops and looks up.



Previous animal studies confirmed that birds such as ravens, starlings, geese, and <a href="https://www.earth.com/news/penguins-are-threatened-by-mercury-contamination/">penguins</a> follow another’s gaze. Yet those experiments almost always involved a pair of birds. 



The Konstanz team wanted to know whether flock size changes the equation for species that live in large groups.



According to Delacoux, pigeons are well-suited to this task because they typically form relatively large flocks, where individuals are usually surrounded by multiple conspecifics. 



"In such flocks, following another’s gaze should be beneficial for key activities such as <a href="https://www.earth.com/news/fish-foraging-behavior-changing-climate-warming-waters/">foraging</a> and vigilance," noted Delacoux.



<h2 class="wp-block-heading" id="h-studying-gaze-with-flocks">Studying gaze with flocks</h2>



To test the idea, the researchers used a state-of-the-art barn near Lake Constance. Two groups of pigeons were placed face-to-face.



One group had an unobstructed view of a gently moving object designed to catch their attention; the other group’s view was blocked by a screen. 



Sophisticated cameras recorded every head movement from several angles, letting the scientists pinpoint to the millisecond when each pigeon oriented toward the hidden object.



The experiment was repeated with various “informed” group sizes. Sometimes just one pigeon could see the object; other times three, five, or more birds had the privileged view. 



The question was whether - and how quickly - the uninformed pigeons would swivel their heads to match the gaze of their companions.



<h2 class="wp-block-heading" id="h-gaze-spreads-with-flock-size">Gaze spreads with flock size</h2>



The results confirmed that pigeons do notice and copy the direction of others’ attention. However, the effect depended heavily on group size. When a lone pigeon stared, few flockmates joined in.



As the number of gazing birds climbed, more and more uninformed birds aligned their vision the same way. 



Unlike Milgram’s human crowds, the researchers did not find a sharp cut-off - no fixed “quorum” that suddenly triggered mass participation. Instead, the likelihood of following grew steadily with each additional pigeon already looking.



Thus, while <a href="https://www.earth.com/news/all-birds-one-tree-complete-evolutionary-map-reveals-hidden-links/">birds</a> responded to collective cues, they did so on a sliding scale rather than an all-or-nothing basis.



<h2 class="wp-block-heading" id="h-understanding-the-pigeon-mind">Understanding the pigeon mind</h2>



Does gaze following in groups mean pigeons understand that their neighbors possess knowledge they lack? Delacoux is cautious. 



“I would not assume that their behavior means any more than that they are just following the gazes of others,” he said.



The birds did not reposition themselves to get a clearer view, for example, a move one might expect if they inferred what another bird could see. 



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/pigeons_gaze_eye-motion_observers_illustration_credit-UKonstanz_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/pigeons_gaze_eye-motion_observers_illustration_credit-UKonstanz_1s.webp" alt="Test setup in the high-tech barn: The pigeons are divided into two groups. Only one group (&quot;demonstrators&quot;) sees the moving object. Does the second group (&quot;observers&quot;) now follow the gaze of their peers? Credit: Mathilde Delacoux" class="wp-image-1977083"/></a><figcaption class="wp-element-caption">Test setup in the high-tech barn: The pigeons are divided into two groups. Only one group ("demonstrators") sees the moving object. Does the second group ("observers") now follow the gaze of their peers? Click image to enlarge. Credit: Mathilde Delacoux</figcaption></figure>



The researchers interpret the response as largely reflexive - an efficient rule of thumb in flock life, rather than evidence of higher-order perspective-taking.



Still, the study illuminates how pigeons use social information. “Now, we know pigeons don’t just copy their flockmates' gaze; they modulate their gaze-following behavior depending on how many peers give a gaze cue,” Kano said. “They respond to a collective cue.”



In other words, a single bird’s glance carries little weight, but a chorus of looks quickly draws the rest of the <a href="https://www.earth.com/news/bird-flocking-dynamics-inspire-advancements-in-technology/">flock</a>’s attention.



<h2 class="wp-block-heading" id="h-gaze-in-social-animals">Gaze in social animals</h2>



The findings underscore the value of studying animals in the social settings where they evolved. As Kano argued, “many animals evolved in groups. To truly understand how they think and communicate, we need to study them in groups, too.”



By mapping the subtle ways that group size shapes behavior, the researchers add a new layer to our understanding of how animals share information and make collective decisions. 



Such insights may apply well beyond pigeons, offering clues to the social cognition of many flocking or herding species, and even echoing back to the street-corner instincts of our own species.



The full study can be found in the journal <a href="https://www.sciencedirect.com/science/article/pii/S2589004225011186" target="_blank" rel="noreferrer noopener">iScience</a>.



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Pigeons exhibit the same behavior as humans by following the gaze of others in their flock

Anyone who has ever stopped on a busy street because...

Chimpanzees are showing us that culture isn't just about tools or survival. A new study at a sanctuary in Zambia has revealed something remarkable. Several chimpanzees began to copy each other by dangling blades of grass from their ears or behinds, for no clear reason. 



The unexpected behavior appeared only in certain <a href="https://www.earth.com/news/social-chimpanzee-mothers-raise-babies-more-successfully/">groups</a>, despite all living in similar environments.



“This shows that, like humans, other animals also copy seemingly pointless behaviors from one another,” said <a href="https://www.uu.nl/en" target="_blank" rel="noreferrer noopener">Utrecht University</a> researcher Edwin van Leeuwen. “And that, in turn, may offer insights into the evolutionary roots of human culture.”



<h2 class="wp-block-heading" id="h-mimicking-others-without-clear-purpose">Mimicking others, without clear purpose</h2>



People often copy odd trends like shaving eyebrow lines or dressing their pets. These habits spread fast but serve no obvious function.



In animals, copying usually relates to survival. <a href="https://www.earth.com/news/chimpanzees-select-the-best-materials-for-termite-fishing/">Chimps</a> teach each other how to crack nuts or fish for termites. But sometimes, animals embrace habits that seem to lack any benefit. Orcas wearing dead salmon as hats is one recent example.



This study focuses on such non-functional behaviors, rarely explored in depth. Back in 2010, a chimpanzee named Julie at <a href="https://www.chimfunshiwildlife.org" target="_blank" rel="noreferrer noopener">Chimfunshi Wildlife Orphanage</a> Trust started putting grass in her ear. Soon, seven others followed. Even after Julie’s death, her group kept the habit.



Researchers saw this as a cultural tradition, as it remained confined to her group and persisted over years. The behavior looked more like a fashion statement than a survival tactic.



Years later, another group at the same sanctuary began doing the same. They had no contact with Julie’s group, ruling out direct copying. Five out of eight chimps in the new group copied the grass-in-ear <a href="https://www.earth.com/news/social-curiosity-starts-young-and-helps-us-survive/">behavior</a>.



<h2 class="wp-block-heading" id="h-chimpanzees-copying-an-odd-trend">Chimpanzees copying an odd trend</h2>



In an unexpected twist, the new group added a unique spin. Six chimps began inserting grass into their behinds, letting it dangle freely. Scientists named this “grass-in-rectum behavior.”



The researchers closely observed the spread of both habits. In August 2023, a chimp named Juma was the first to do both <a href="https://www.earth.com/news/chimpanzees-use-rhythmic-drumming-to-communicate-in-forests/">behaviors</a>. 



Within a week, four others copied the grass-in-ear trick. Within six weeks, five others copied the grass-in-rectum behavior. This happened without external prompting or visible irritation in their ears or behinds.



<h2 class="wp-block-heading" id="h-evidence-of-social-learning">Evidence of social learning</h2>



The researchers analyzed how these behaviors spread within the groups. They used a statistical method called Network-Based Diffusion Analysis (NBDA).



The analysis showed that both behaviors spread mainly through social learning. In fact, over 80% of the chimps adopted them through copying others. Social ties strongly predicted who picked up the habits first.



Interestingly, even new chimps integrated into the group later copied the grass-in-ear habit within months.



<h2 class="wp-block-heading" id="h-chimpanzees-may-copy-humans">Chimpanzees may copy humans</h2>



The researchers also considered the role of humans. Both chimp groups with these behaviors shared the same caregivers. 



The caregivers sometimes cleaned their ears with grass or sticks. Other groups with different caregivers did not develop such habits.



“The chimps in the one group then figured out to stick the blade of grass in another place as well,” said Van Leeuwen.



In the wild, such trends are absent among chimpanzees. Captivity offers more free time and fewer survival pressures. That might explain why chimps experiment with odd habits there.



“Why they do exactly this particular thing, I’m not really concerned about. But them copying the behaviour from each other, that is the important insight,” noted Van Leeuwen.



<h2 class="wp-block-heading" id="h-lessons-for-human-culture">Lessons for human culture</h2>



Some scientists think humans evolved culturally because we copy tiny details, even useless ones. Animals supposedly cannot do this, yet the study suggests otherwise.



“Our study shows that chimpanzees are able to copy small, useless behaviors from each other,” said Jake Brooker from Durham University. “That is why we felt it was important to share these new observations.”



Van Leeuwen’s team noted that these behaviors may not be entirely useless. They might serve as social signals.



“It could also serve a social purpose. By copying someone else’s behavior, you show that you notice and maybe even like that individual. So, it might help strengthen social bonds and create a sense of belonging within the group, just like it does in humans,” said Van Leeuwen.



The researchers also suggest these behaviors may reflect a deep social drive. Young chimps often form alliances and bonds through mimicry. In this case, lower-ranking males copied higher-ranking ones, likely to gain approval.



<h2 class="wp-block-heading" id="h-chimps-may-copy-for-social-reasons">Chimps may copy for social reasons</h2>



Scientists propose that copying odd behaviors might help chimps integrate socially. Just like humans, they may copy group norms to build trust and reduce conflict.



One theory, the Zone of Proximal Acquisition, suggests that animals copy behaviors they can already physically perform but haven’t yet tried in that exact way. The grass behaviors fit this model well.



Another theory, the Zone of Bounded Surprisal, suggests animals are drawn to behaviors that surprise them yet feel familiar. Chimps already examine each other’s behinds frequently, making this behavior more noticeable and likely to spread.



<h2 class="wp-block-heading" id="h-chimps-have-complex-social-lives">Chimps have complex social lives</h2>



The findings challenge long-held views about animals’ cultural limits. Chimps show they can adopt unusual, non-functional behaviors through social learning. Whether these habits offer hidden social benefits remains to be seen.



Still, the very act of copying and passing down such behaviors highlights the complexity of animal cultures. It suggests that even seemingly pointless acts may hold value in the social lives of chimpanzees.



The study is published in the journal <a href="https://brill.com/view/journals/beh/aop/article-10.1163-1568539X-bja10313/article-10.1163-1568539X-bja10313.xml" target="_blank" rel="noreferrer noopener">Behaviour</a>.



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Chimpanzees copy strange, useless trends just like humans do

Chimpanzees are showing us that culture isn't just about tools...

Two small, sand‑colored nymphs of the seldom‑seen mayfly Behningia baei surfaced from the Mae Chaem River in northern Thailand during a December 2024 field survey. 



The find ends a 22‑year drought of sightings and puts the insect back on scientists’ maps after generations of silence in entomological records.



Until now the species, first described in 2006 from a site about 250 miles to the south, had vanished from every subsequent expedition. 



The rediscovery team was led by <a href="https://www.researchgate.net/profile/Sedtawut-Kwanboon" target="_blank" rel="noreferrer noopener">Sedtawut Kwanboon</a> and <a href="https://www.researchgate.net/profile/Boonsatien-Boonsoong" target="_blank" rel="noreferrer noopener">Boonsatien Boonsoong</a> of <a href="https://www.ku.ac.th/en/community-home" target="_blank" rel="noreferrer noopener">Kasetsart University</a>, Bangkok.



<h2 class="wp-block-heading" id="h-why-behningia-was-in-the-sand">Why Behningia was in the sand</h2>



Most <a href="https://www.britannica.com/animal/mayfly" target="_blank" rel="noreferrer noopener">mayfly</a> work chases fluttering adults, yet the Thai team instead scuffed the riverbed with kick nets, stirring up juveniles hidden like grains of rice in the fine sediment. 



Burrowing youngsters cling to loose sand where sunlight and predators rarely reach, making them easier to sample than their airborne parents.



After hours of microscope work, every mandible, leg, and gill on the two specimens matched the 2006 description of B. baei. High‑resolution images confirmed the identity beyond doubt.



“These new data about the geographic and habitat distributions of behningiid mayflies helps to fill knowledge gaps and improves our ability to address conservation issues surrounding these rarely seen mayflies, not only in Thailand but also globally,” wrote Boonsatien Boonsoong. 



The quote hints at how a single rediscovery can redraw conservation priorities far beyond one stream.



The <a href="https://www.tripadvisor.com/Tourism-g790338-Mae_Chaem-Vacations.html" target="_blank" rel="noreferrer noopener">Mae Chaem site</a> sits about 1,350 feet above sea level and 250 miles north of the original locality in <a href="https://www.tourismthailand.org/Destinations/Provinces/Phitsanulok/112" target="_blank" rel="noreferrer noopener">Phitsanulok Province</a>. That span suggests the insect occupies more rivers than anyone ever suspected.



<h2 class="wp-block-heading" id="h-sand-dwelling-mayflies">Sand‑dwelling mayflies</h2>



Mayflies move the energy stored in algae to fish, birds, and other animals. They achieve this by grazing as juveniles and then by becoming prey along nearly every link of the freshwater food web.



Because nymphs breathe through exposed gills, they suffocate in low‑oxygen or polluted streams, so biologists use their numbers as a living <a href="https://pubs.usgs.gov/publication/70195672" target="_blank" rel="noreferrer noopener">water‑quality score</a>. 



Locating B. baei confirms that the Mae Chaem reach still carries clean, oxygen‑rich water over stable sand.



While every mayfly supports predators, sand‑burrowing families such as Behningiidae also churn and aerate the top inch of sediment. Their digging loosens grains and speeds nutrient exchange, turning them into tiny ecosystem engineers.



<h2 class="wp-block-heading" id="h-behningia-s-life-measured-in-hours">Behningia's life measured in hours</h2>



Mayflies belong to the order <a href="https://bugguide.net/node/view/78" target="_blank" rel="noreferrer noopener">Ephemeroptera</a>, a name that nods to adult lives frequently shorter than a single day. Most adult mayflies survive only 48–72 hours, with some species lasting barely ninety minutes.



The champion of brevity, the North American <a href="https://georgiabiodiversity.org/portal/profile?group=all&amp;es_id=21325" target="_blank" rel="noreferrer noopener">Dolania americana</a>, holds the record at under five minutes for adult females. Such fleeting adulthood explains why researchers almost never catch rarities like B. baei on the wing.



By focusing on juveniles, the Thai team sidestepped that scheduling nightmare. The method also avoids killing breeding adults, an ethical bonus when populations appear thin.



The <a href="https://www.earth.com/news/fish-thought-extinct-for-85-years-reappears-in-himalayan-river-chel-snakehead/">rediscovery</a> underscores how insect timelines differ from human ambitions. Two decades to us equal perhaps twenty complete life cycles for B. baei, enough time for habitats to vanish or rebound.



<h2 class="wp-block-heading" id="h-what-the-rediscovery-tells-conservationists">What the rediscovery tells conservationists</h2>



Thailand lists more than 300 mayfly species, yet only one other Behningia species, <a href="https://publication.plazi.org/GgServer/html/E47AD7D9ECE556F7863FE00403810630/3" target="_blank" rel="noreferrer noopener">Protobehningia merga</a>, was previously noted in the Mae Chaem basin. Finding both taxa in one river shows that fine‑sand beds remain a refuge worth guarding.



The study’s distribution map extends B. baei nearly 250 miles northward, hinting that tropical Behningiidae can tolerate cooler upland currents. That clue will guide future surveys toward similar sandy reaches.



River managers in Southeast Asia often focus on charismatic megafauna, but tiny <a href="https://www.macroinvertebrates.org/" target="_blank" rel="noreferrer noopener">macroinvertebrate</a> indicators flag trouble years earlier. Adding routine kick‑net checks to water‑quality programs could save money and species alike.



<h2 class="wp-block-heading" id="h-what-s-next-for-behningia-baei">What's next for Behningia baei</h2>



Kwanboon plans DNA bar‑coding of the two specimens to confirm there is no cryptic sibling <a href="https://www.earth.com/news/earth-may-have-three-million-undiscovered-animal-species/">species</a> hiding under the same name. He also hopes to sample neighboring tributaries before the next monsoon blankets sites in turbid runoff.



Meanwhile, the team is training local students to run simple kick‑net protocols so discoveries will not depend on brief visits by city scientists. Community observers could turn rare rediscoveries into routine data points.



Sand bars, often overlooked by conservation rules, shelter specialized <a href="https://www.earth.com/news/animals-found-to-have-a-sixth-sense-gecko-hearing-vibrations-changing-science-view-of-sound/">animals</a> that vanish if substrates shift even a few inches. Keeping those substrates stable may prove as vital as controlling chemical pollutants.



For a creature that spends most of its life buried and the rest aloft on borrowed minutes, reappearing after two decades is indeed dramatic. Yet the authors treat it as the first chapter of a longer investigation, not the final page.



The study is published in <a href="https://checklist.pensoft.net/article/148597/" target="_blank" rel="noreferrer noopener">Check List</a>.



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Rare insect that was thought to be extinct for 20 years was rediscovered

Two small, sand‑colored nymphs of the seldom‑seen mayfly Behningia baei...

Horses are helping fill a major gap in mental health care for children. With long waitlists and limited success from traditional talk therapy, many kids are still falling through the cracks. 



For some, sitting in a therapist’s office just doesn’t work. But therapy sessions held outdoors, with horses as part of the team, are starting to make a real difference.



A recent study from the <a href="https://www.unisa.edu.au/">University of South Australia</a> shows that equine-assisted therapy is shifting the way social workers support children. The research highlights the experiences of ten professionals already using horses to connect with kids in powerful ways.



<h2 class="wp-block-heading" id="h-horse-therapy-in-nature">Horse therapy in nature</h2>



Equine-assisted interventions (EAI) are a form of therapy that brings children and horses together in natural, outdoor settings. 



The sessions are led by trained <a href="https://www.earth.com/news/exercise-reduces-depression-and-anxiety-in-children-and-teens-with-mental-health-issues/">mental health</a> professionals working alongside experienced equine practitioners. And the results, according to those involved, can be transformative.



The study found that <a href="https://www.earth.com/news/supportive-adults-help-protect-children-from-mental-health-issues/">children</a> often connect more easily in this environment than they do in traditional therapy rooms. The calm of nature, the presence of horses, and the physical space to move and breathe - these all contribute to a sense of safety and openness.



<h2 class="wp-block-heading" id="h-children-trust-horses">Children trust horses</h2>



Morgyn Stacy, a University of South Australia Social Work graduate who led the study as part of her Honors project, noted that conventional talk therapy doesn’t work for every child.



“But give them the <a href="https://www.earth.com/news/how-nature-heals-outdoor-activities-greatly-improve-mental-health/">space</a> to be outside, to connect with a horse, and something powerful happens. They begin to feel safe, calm, and ready to open up,” noted Stacy.



The connection doesn’t happen by chance. Horses are naturally sensitive to human emotions and body language. 



The horses reflect the <a href="https://www.earth.com/news/words-shape-how-our-brains-process-feelings-and-guide-decisions/">feelings</a> of the child standing next to them. This mirroring effect can help children understand and manage their emotions in ways they haven’t before.



One practitioner in the study described the experience as “being seen through the eyes of a horse,” a kind of connection that can shift something deep inside a child.



<h2 class="wp-block-heading" id="h-extended-benefits-of-horse-therapy">Extended benefits of horse therapy</h2>



Therapists working in these settings don’t just use the horses - they also use the land. Sessions might include walking barefoot in sand, noticing animal tracks, or standing quietly with a horse. These simple activities help children feel grounded and present.



"The benefits go beyond mental health," said Stacy. "Children often gain confidence, improve communication skills, and build stronger emotional resilience."



Some kids even come in afraid of horses. Therapists help them work through those fears by matching them with the right animal. And when a child overcomes that fear, it becomes a confidence boost they can carry into other areas of life.



<h2 class="wp-block-heading" id="h-horses-can-help-kids-with-trauma">Horses can help kids with trauma</h2>



Dr. Fatin Shabbar, a senior researcher at the University of South Australia and a qualified social worker, said this approach can be especially helpful for children who have experienced <a href="https://www.earth.com/news/childhood-trauma-can-cause-physical-pain-in-late-life/">trauma</a>, such as those in the child protection system.



"Practitioners in the study described deeply moving examples of children bonding with horses in ways that sparked emotional breakthroughs where other therapies had failed," said Dr. Shabbar.



But this kind of therapy isn’t widely available. It costs a lot to care for horses and maintain rural therapy spaces. Without funding support - from programs like the NDIS or child protection services - many families just can’t afford it.



<h2 class="wp-block-heading" id="h-need-for-recognition-and-guidelines">Need for recognition and guidelines</h2>



Despite its potential, equine-assisted therapy still faces major roadblocks. The absence of national standards in Australia means there's no consistent guarantee of practitioner training - raising serious concerns about the safety of both children and animals.



"Another concern is the lack of regulation in Australia," said Dr. Shabbar. "Without clear guidelines, unqualified practitioners may offer equine-assisted services without appropriate training, which puts both children and the animals at risk."



Even highly qualified professionals face an uphill battle. The therapy isn’t formally recognized as evidence-based in many settings.



"This research shows that equine-assisted therapy can be a deeply healing experience. But for it to reach more children, we need formal recognition, ethical guidelines and proper funding," noted the authors of the study. 



<h2 class="wp-block-heading" id="h-rethinking-what-healing-looks-like">Rethinking what healing looks like</h2>



This study isn’t just about horses. It’s about expanding how we think about healing. It’s about listening to the people on the ground - therapists, social workers, and most importantly, the kids - who are saying that there’s another way to do things.



With the right support, equine-assisted therapy could become more than a niche offering. It could become a trusted option for children who need something different, something real, and something that works.



The full study was published in the journal <a href="https://www.tandfonline.com/doi/full/10.1080/02650533.2025.2495741">Journal of Social Work Practice</a>.



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Therapy horses are helping children heal from trauma

Horses are helping fill a major gap in mental health...

While age may bring wisdom for people, it appears to bring peril for white-lined sphinx moths. A recent field study shows that birds, rodents, and other predators are far more likely to peck, bite, or maul these insects once they emerge from the pupal stage and spread their wings.



Led by the <a href="https://www.utep.edu/">University of Texas at El Paso</a> (UTEP), the research lends experimental weight to a long-standing evolutionary idea. Complete metamorphosis may protect youthful stages from predation, allowing individuals to reach reproductive maturity before facing the most dangerous chapter of life.



<h2 class="wp-block-heading" id="h-caterpillars-versus-adult-moths">Caterpillars versus adult moths</h2>



Biologist Brett Seymoure, principal investigator and assistant professor at UTEP, studies holometabolous insects - species that pass through egg, larva, pupa, and adult phases.



The prevailing theory suggests that <a href="https://www.earth.com/news/dragonfly-larvae-expose-climates-hidden-influence-on-biology/">larvae</a> enjoy a relative sanctuary from predators, giving them a chance to grow before adulthood brings mobility, exposure, and heightened risk.



“There are multiple hypotheses about why these insects go through so many stages before reaching adulthood,” Seymoure said.



“Our research set out to test the prediction that caterpillars are less likely to be attacked by predators, enabling the insect to survive to adulthood and reproduce before it has to face the most dangerous part of its life.”



<h2 class="wp-block-heading" id="h-creating-life-sized-decoys">Creating life-sized decoys</h2>



Directly observing countless <a href="https://www.earth.com/news/largest-predator-prey-feast-ever-seen-in-the-ocean-enormous-quickly-altered-food-chain/">predator attacks</a> on real moths would be impractical. Instead, graduate student and lead author Braulio Alexis Sanchez created convincing clay replicas of both caterpillars and adult moths.



To mimic the wing patterns of Hyles lineata accurately, he printed photographs on special paper calibrated for precise color matching, then attached the wings to the clay bodies. 



Because clay records punctures and impressions, each model would serve as a forensic logbook, revealing encounters with sharp beaks or probing mandibles.



<h2 class="wp-block-heading" id="h-moths-meet-predators-in-texas">Moths meet predators in Texas</h2>



The team installed pairs of decoys - one caterpillar, one adult - on creosote bushes scattered across the rugged Indio Mountains Research Station in West Texas, a property managed by UTEP. 



Spacing the models closely ensured they faced identical environmental conditions. Over three consecutive days, researchers visited sites at dawn and dusk, inspecting every replica for new damage, counting beak marks, tooth gouges, or missing segments.



“Out of 70 replicas that were attacked, 50 were adults and 20 were caterpillars, and most of the attack marks were consistent with birds,” noted Sanchez.



In other words, adult-shaped models were assaulted two and a half times more often than larval shapes. Because both forms were equally available to predators, the data point toward active selection: visually oriented hunters seemed to prefer the adult silhouette.



<h2 class="wp-block-heading" id="h-predators-prefer-winged-moths">Predators prefer winged moths</h2>



The results bolster the notion that larval life provides a safer developmental window. If predation focused primarily on caterpillars, populations might struggle to produce enough breeding adults.



“If moths in the <a href="https://www.earth.com/news/caterpillars-inherit-food-preferences-through-their-blood/">caterpillar</a> stage were more heavily attacked, it would be much more difficult for moths to reach adulthood and reproduce,” Seymoure noted. 



Instead, the danger spikes only when the moth takes wing - precisely when reproduction becomes possible.



<h2 class="wp-block-heading" id="h-a-reminder-of-insect-importance"><a></a>A reminder of insect importance</h2>



Beyond theoretical interest, the study highlights insects’ ecological centrality. As Sanchez put it, “Without insects, there are no humans, trees, or plants.”



<a href="https://www.earth.com/news/insects-are-still-disappearing-and-there-are-hundreds-of-reasons-why/">Insects</a> pollinate crops, decompose organic matter, seed food webs, and cycle nutrients. Yet global surveys report worrying declines. 



Understanding at what life stage insects are most vulnerable can inform habitat management, pesticide timing, and conservation priorities.



<h2 class="wp-block-heading" id="h-identifying-the-moth-s-predators">Identifying the moth's predators</h2>



While bite impressions suggested birds were the main culprits, the researchers plan to broaden their surveillance.



Nocturnal moth predators - <a href="https://www.earth.com/news/frog-mating-calls-teach-bats-which-prey-to-avoid/">bats</a>, rodents, even wandering spiders - might attack under cover of darkness. 



Motion-activated cameras, night-vision optics, and ultrasonic detectors could capture real-time predation events and complement the static clay evidence.



The Chihuahuan Desert hosts unique avian assemblages and sparse vegetation, potentially exaggerating visual hunting cues. To test generality, Seymoure’s team hopes to replicate experiments in woodland, grassland, and urban settings, and with different moth species.



If adult-biased predation proves universal, it would underscore metamorphosis as a widespread risk-management strategy in insects.



<h2 class="wp-block-heading" id="h-maturity-invites-greater-danger">Maturity invites greater danger</h2>



Complete metamorphosis remains one of evolution’s most ingenious inventions, separating growth and reproduction into distinct anatomical phases.



The new findings suggest an additional benefit: by bottling youth within a relatively inconspicuous caterpillar, nature minimizes early-life losses. 



Once it stockpiles resources and unfurls its wings, the adult embarks on the perilous business of mating and dispersal. For Hyles lineata, growing older quite literally means stepping into the firing line.



<h2 class="wp-block-heading" id="h-focusing-on-climate-and-scent">Focusing on climate and scent</h2>



Future studies may integrate chemical cues - some predators use scent rather than sight - or assess how <a href="https://www.earth.com/news/danger-zones-climate-change-is-altering-predator-prey-dynamics/">climate change</a> alters predator-prey dynamics.



For now, the clay decoys at Indio Mountains recount a simple story: in the desert sky, an adult moth is a conspicuous, protein-rich morsel, while a plump caterpillar clinging to creosote is more likely to pass unnoticed. 



Age, it seems, is more than just a number for these shapeshifting insects; it marks the difference between relative safety and a sudden, predatory strike.



The study is published in the journal <a href="https://www.mdpi.com/2075-4450/16/4/347">Insects</a>.



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Why predators attack adult moths instead of caterpillars

While age may bring wisdom for people, it appears to...

Gender dynamics among primates have long fascinated both scientists and the public. Many people assume that male dominance over females is natural across primates, a belief that also shapes how we think about human gender roles. However, a new study challenges this view. 



Conducted by researchers from the University of Montpellier, the Max Planck Institute for Evolutionary Anthropology, and the <a href="https://www.google.com/search?client=safari&amp;rls=en&amp;q=German+Primate+Center&amp;ie=UTF-8&amp;oe=UTF-8" target="_blank" rel="noreferrer noopener">German Primate Center</a>, the work sheds light on the surprising flexibility of power relations among primates.



The findings reveal that neither male nor female dominance is universal. Instead, power shifts depend on factors such as ecology, reproductive strategies, and social structures. The study spans 253 populations from 121 primate species, making it the largest of its kind.



The results call for a reconsideration of our assumptions - not only about other primates but also about ourselves. The study highlights how gendered power dynamics emerge through complex, evolving interactions.



<h2 class="wp-block-heading" id="h-why-power-matters-in-primates">Why power matters in primates</h2>



The researchers examined patterns of aggression between males and females in <a href="https://www.earth.com/news/chimpanzees-select-the-best-materials-for-termite-fishing/">primates</a>. They discovered that nearly half of all aggressive encounters occur between opposite sexes.



This finding contrasts with previous studies that focused mostly on same-sex competition. These older views assumed that males and females compete for different resources, leading to separate social hierarchies.



“The observation that, in most populations, any given individual is more likely to be involved in a fight against another individual of the opposite rather than the same sex highlights that the battle of the sexes is common in other animals,” said Dieter Lukas from the Max Planck Institute.



The researchers then studied the outcomes of these conflicts to identify whether males or females tend to dominate.



<h2 class="wp-block-heading" id="h-male-dominance-is-rare-in-primates">Male dominance is rare in primates</h2>



Traditionally, many assumed that male dominance is the default in <a href="https://www.earth.com/news/laughter-lifts-bonobo-moods-offering-clues-to-human-emotion/">primate</a> societies. Iconic cases like female-dominant bonobos or lemurs were seen as rare exceptions.



Yet this study revealed a more complex picture. Among the 151 primate populations with quantitative data, only 17 percent showed strict male dominance. In comparison, 13 percent showed strict female dominance.



The remaining 70 percent of populations displayed moderate or no clear dominance by either sex. 



“Recent research started to challenge the traditional views of male dominance being the default status, and our study now provides a more comprehensive exploration of variation in intersexual dominance relationships," noted Peter Kappeler from the German Primate Center.



The research marks a major shift from old assumptions, showing that rigid male dominance is far less common than once believed.



<h2 class="wp-block-heading" id="h-when-female-primates-take-charge">When female primates take charge</h2>



To explain these varied outcomes, the researchers tested five hypotheses. The strongest support emerged for the reproductive control hypothesis.



In species where females gain more control over reproduction, they are more likely to dominate socially as well. This pattern appears in species that are monogamous, arboreal, or where males and females are similar in size.



In such species, females can often reject male advances. They also tend to live in environments that allow them to avoid physical coercion.



Female dominance also flourishes in societies with high female-female <a href="https://www.earth.com/news/what-animal-will-replace-humans-as-earths-dominant-species-this-scientist-has-an-idea/">competition</a>. This includes pair-living or solitary species where females are territorial and fiercely guard resources.



Interestingly, female dominance often coincides with low sexual dimorphism, short periods of sexual receptivity, and balanced sex ratios within groups.



<h2 class="wp-block-heading" id="h-where-male-primates-keep-power">Where male primates keep power</h2>



Conversely, male-biased dominance typically appears in terrestrial, polygynous species with high sexual dimorphism. In these societies, males dominate through sheer physical power.



“Critically, while primate males gain power via physical force and coercion, female empowerment relies on alternative pathways, such as reproductive strategies to gain control over matings,” noted Elise Huchard from the <a href="https://www.umontpellier.fr/en/" target="_blank" rel="noreferrer noopener">University of Montpellier</a>.



This pattern often involves larger male body size, specialized weapons like large canines, and polygynous mating systems. Terrestrial species are especially prone to this male-dominated structure, as females have fewer opportunities to escape or resist male control.



The findings reveal that the ecological context - whether arboreal or terrestrial - shapes the way power is exercised.



<h2 class="wp-block-heading" id="h-female-power-shifts-within-primates">Female power shifts within primates</h2>



One striking discovery is that dominance patterns often vary within a species. The study revealed wide-ranging variation in female dominance across different populations of the same species.



For example, in bonobos, females win between 48 percent and 79 percent of contests with males, depending on the group. Other species show similar variation, proving that social dynamics can shift based on local conditions.



Some species even display all three dominance types - female-biased, male-biased, and neutral - across different groups.



The researchers also noted a clear link between evolutionary history and dominance patterns. Great apes and African and Asian monkeys tend to show male-biased dominance, while lemurs and lorises frequently show female dominance. New World monkeys often fall somewhere in between.



<h2 class="wp-block-heading" id="h-competition-and-female-dominance">Competition and female dominance </h2>



Another major finding comes from testing the female competition hypothesis. The study found that species with intense female-female competition often show female-biased dominance.



Such competition appears frequently in pair-living or solitary species where females exclude rivals from resources. Female dominance also tends to emerge in stable social groups where female conflicts over food are common.



Interestingly, ecological harshness and environmental unpredictability were not strong predictors of female dominance, despite past claims to the contrary.



Instead, social structure and mating systems - such as group stability and reproductive strategies - emerged as stronger influences.



<h2 class="wp-block-heading" id="h-female-parenting-and-primate-power">Female parenting and primate power</h2>



The study also explored the offspring safety hypothesis, which links dominance to <a href="https://www.earth.com/news/orangutan-mothers-have-unique-parenting-styles-like-humans/">parenting</a> strategies. It found that female-biased dominance is more common in species where mothers park their young rather than carrying them constantly.



Species with shorter lactation periods and lower risks of male-inflicted infanticide also tend to show greater female dominance. These traits reduce the cost of engaging in risky conflicts with males.



Interestingly, allomaternal care, where other group members help care for infants, also plays a role in shaping power dynamics.



<h2 class="wp-block-heading" id="h-social-bonds-and-female-dominance">Social bonds and female dominance </h2>



Researchers also tested whether female social bonds, such as coalition formation, explain female dominance. Their findings showed only limited support for this idea.



While female philopatry - where females remain in their birth group - was linked to greater female dominance, this pattern was not strongly tied to coalition formation.



This challenges theories that female alliances drive dominance in species like bonobos. The authors suggest that in many cases, sex-biased dispersal may be a result of dominance structures rather than their cause.



<h2 class="wp-block-heading" id="h-new-view-of-power-and-evolution">New view of power and evolution</h2>



The findings offer a profound shift in how we think about male and female <a href="https://www.earth.com/news/most-endangered-primate-species-identified-in-new-report/">primates</a> - and humans - by revealing that dominance is not fixed by nature but shaped by many intertwined factors.



Female power often emerges through reproductive strategies, social competition, and ecological flexibility. Male dominance, on the other hand, typically relies on brute force, physical coercion, and ecological constraints.



By showing that female dominance is neither rare nor accidental, this research opens the door to new ways of thinking about gender roles. 



Ultimately, the study highlights that both male and female dominance can emerge through different routes, depending on specific ecological and social pressures.



The study is published in the journal <a href="https://www.pnas.org/doi/10.1073/pnas.2500405122" target="_blank" rel="noreferrer noopener">Proceedings of the National Academy of Sciences</a>.



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Female dominance in primates is more common than we thought

Gender dynamics among primates have long fascinated both scientists and...

Insects are being harmed by a fungicide sprayed on fruits and vegetables - even at levels that are considered safe. 



A new study from <a href="https://www.mq.edu.au/" target="_blank" rel="noreferrer noopener">Macquarie University</a> reveals that the chemical chlorothalonil, which is used globally to prevent fungal disease, is damaging insect fertility and survival.



<h2 class="wp-block-heading" id="h-testing-the-fungicide-on-fruit-flies">Testing the fungicide on fruit flies</h2>



Researchers at Macquarie’s School of Natural Sciences tested the effects of chlorothalonil on <a href="https://www.earth.com/news/fruit-flies-can-walk-jump-and-dance-using-the-same-motor-neurons/">fruit flies</a>, a common insect model used in labs. Fruit flies are representative of a large number of similar insect species in the wild.



The team used <a href="https://www.earth.com/news/for-the-first-time-scientists-have-genetically-engineered-virgin-births/">Drosophila melanogaster</a>, known as the common fruit fly or vinegar fly. Unlike pests that target crops, these flies feed on rotting fruit. They play an important role in breaking down waste and recycling nutrients on farms and in orchards.



“D. melanogaster is also at the bottom of the food chain, becoming food for a whole lot of other species,” said Ph.D. candidate Darshika Dissawa, lead author of the research paper.



<h2 class="wp-block-heading" id="h-a-surprising-decline-in-insect-fertility">A surprising decline in insect fertility</h2>



The experiment exposed fruit fly larvae to chlorothalonil at levels that match what’s found on real agricultural produce, such as cranberries and wine grapes. What they found shocked the team.



“Even the very lowest concentration has a huge impact on the reproduction of the flies that we tested,” said Dissawa. “This can have a big knock-on population impact over time because it affects both male and female fertility.”



Flies exposed to the chemical showed a 37% drop in egg production at maturity, compared to those that were not exposed.



“We expected the effect to increase far more gradually with higher amounts. But we found that even a very small amount can have a strong negative effect,” noted Professor Fleur Ponton.



<h2 class="wp-block-heading" id="h-fungicide-still-in-use-despite-risks">Fungicide still in use, despite risks</h2>



Chlorothalonil is <a href="https://www.europarl.europa.eu/doceo/document/E-9-2024-000263_EN.html">banned</a> in the European Union. But in Australia, it’s still sprayed widely to stop fungal diseases like <a href="https://www.earth.com/news/disease-attacking-blueberry-plants-is-spreading-around-the-world/">mildew</a> and leaf blight.



Residue from this fungicide has been found in soils and water near farms. On food, the levels can range from almost zero to 460 milligrams per kilogram.



“Chlorothalonil is particularly common in orchards and vineyards, and is often used preventatively when no disease is present,” explained Professor Ponton. 



“People assume <a href="https://www.earth.com/news/wild-birds-are-significantly-threatened-by-vineyard-fungicides/">fungicides</a> like chlorothalonil only impact fungal diseases, but they can have devastating, unintended consequences for other species,” she stated.



<h2 class="wp-block-heading" id="h-fungicide-fuels-insect-decline">Fungicide fuels insect decline </h2>



The study revealed that chlorothalonil exposure during the larval stage caused major reproductive issues in the adult flies.



Female flies were smaller, had fewer egg-producing structures, and laid far fewer eggs. Male flies had lower iron levels, which can interfere with sperm production and other metabolic functions.



The researchers also checked whether the flies were avoiding the contaminated food. They weren’t.



“We didn’t find a significant aversion for food contaminated with chlorothalonil, except when there was a very high concentration of the chemical,” explained Professor Ponton. “This means the impacts are due to chlorothalonil ingestion.”



<h2 class="wp-block-heading" id="h-effects-on-insect-pollinators">Effects on insect pollinators</h2>



In agricultural settings where whole crops are treated with fungicides, insects like flies and bees have no way to avoid the chemicals. This creates a larger problem for <a href="https://www.earth.com/news/parasitic-plant-has-some-unlikely-allies-for-pollination-and-seed-dispersal/">pollination</a>, ecosystem stability, and food production.



“We need <a href="https://www.earth.com/news/some-bees-value-quality-over-quantity-in-flower-selection/">bees</a> and flies and other beneficial insects for pollination, and we think this is an important problem for pollinator populations,” said Professor Ponton. “There is a strong commercial incentive to understand the impact in the field and address the use of this chemical.”



Despite the widespread use of <a href="https://www.publiceye.ch/en/topics/pesticides/chlorothalonil-a-banned-pesticide-exported-from-europe">chlorothalonil</a>, there's a surprising lack of research into how it affects insects. Fewer than 25 scientific studies have examined this - far too few, considering the global decline in insect numbers.



<h2 class="wp-block-heading" id="h-a-call-for-smarter-farming">A call for smarter farming</h2>



The team behind the study says it’s time to rethink how fungicides are used in agriculture. Reducing the frequency of spraying could give insect populations a chance to recover. But that requires more research.



“We need field trials to explore options and develop evidence-based guidelines to consider the knock-on effects of fungicides on beneficial insects,” said Professor Ponton.



Next, the researchers will study whether these reproductive problems are passed on to future generations. 



The team also plans to investigate what happens when insects are exposed to combinations of chemicals - something that’s far more common in real-world farming.



The full study was published in the journal <a href="https://royalsocietypublishing.org/doi/10.1098/rsos.250136" target="_blank" rel="noreferrer noopener">Royal Society Open Science</a>.



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How crop protection is fueling the global decline of insects

Insects are being harmed by a fungicide sprayed on fruits...

Pollinators are vital for the natural world. They help plants reproduce, support food webs, and sustain ecosystems. Among them, honey bees hold a special place. 



Honey bees are widely celebrated for their role in agriculture and are often seen as environmental heroes. However, their growing presence in places where they are not native raises new concerns.



Southern California is a well-known biodiversity hotspot. It is home to hundreds of native pollinator species. But this unique region now faces a quiet threat. 



Feral honey <a href="https://www.earth.com/news/world-bee-day-2025-protecting-the-pollinators-that-feed-the-world/">bees</a>, thriving outside human control, have begun to dominate pollination networks here. Their influence extends far beyond what most people realize.



A new study from <a href="https://ucsd.edu" target="_blank" rel="noreferrer noopener">University of California San Diego</a> sheds light on this issue. The research uncovers how honey bees, despite their benefits, may unintentionally harm native pollinators. The findings challenge common perceptions and bring attention to a growing ecological conflict.



<h2 class="wp-block-heading" id="h-honey-bees-outcompete-native-pollinators">Honey bees outcompete native pollinators </h2>



Honey bees are highly effective <a href="https://www.earth.com/news/how-bumble-bees-are-sabotaging-their-own-health/">pollinators</a>. They have been introduced worldwide to support crop production. In the U.S., they are responsible for pollinating crops that contribute billions of dollars to the economy each year.



Their ability to communicate allows them to locate and exploit floral resources efficiently. They share information about flower locations with their colony mates, which makes them powerful foragers. Unlike most native bees, honey bees live in large colonies that work together to gather resources.



Because of their efficiency, honey bees outcompete many native bees. They can strip flowers of pollen and nectar quickly. 



Studies show that in Southern California, honey bees now represent nearly 90% of all bees visiting flowers. This leaves little for the region’s diverse native bee <a href="https://www.earth.com/news/rising-dangers-threaten-the-survival-of-bees-and-pollinators/">species</a>, which rely on the same resources.



<h2 class="wp-block-heading" id="h-scale-of-the-honey-bee-invasion">Scale of the honey bee invasion</h2>



The study found that honey bees now make up 98% of total bee biomass in Southern California’s scrublands. This is not just about numbers. Honey bees are much larger than most native bees in this region. Their dominance extends both in terms of individuals and body size.



One reason for this imbalance is the honey bees' remarkable ability to remove pollen. The research showed that honey bees can remove up to 80% of pollen from flowers within just one day. 



In experiments, just two visits by honey bees stripped over 60% of pollen from flowers of native plants like black sage, white sage, and distant phacelia.



Such high pollen removal rates mean that other bees have far fewer resources left. Native <a href="https://www.earth.com/news/native-bee-species-face-extinction-due-to-honey-bee-competition/">bees</a>, many of which are solitary and less efficient foragers, simply cannot compete at this scale.



<h2 class="wp-block-heading" id="h-honey-bees-and-pollen-resources">Honey bees and pollen resources </h2>



Pollen is critical for bee reproduction. Bees collect pollen to feed their larvae. When honey bees take most of the pollen, native bees struggle to raise their young.



The study estimated the daily impact of honey bees on pollen resources. In one hectare of habitat, honey bees removed enough pollen each day to potentially raise hundreds to thousands of native bees. 



Over an entire bloom season, this could result in the loss of tens of thousands of potential native bee offspring.



This finding is alarming. It highlights how honey bees, though often viewed positively, may reduce native bee populations by monopolizing food sources.



<h2 class="wp-block-heading" id="h-larger-bees-face-greater-risks">Larger bees face greater risks</h2>



Interestingly, larger native bees appear to be most affected. The study found that only a tiny fraction of native bees were larger than honey bees. Bumble bees, for instance, made up just 0.1% of all bees observed.



Larger bees generally require more pollen to raise their offspring. When honey bees deplete resources, these species may be pushed out first.



“Although honey bees are rightly considered an indispensable asset to humans, they can also pose a serious ecological threat to natural ecosystems where they are not native,” said Hung.



The loss of large bees could also reduce the effectiveness of pollination. These bees tend to carry more pollen per visit, which benefits many plants.



<h2 class="wp-block-heading" id="h-honey-bees-vs-native-pollinators">Honey bees vs. native pollinators</h2>



The damage does not stop with bees. The study also highlights that honey bee pollination leads to poorer plant offspring quality compared to native bee pollination.



This happens because honey bees often visit many flowers on the same plant before moving to another. This behavior increases the chances of self-pollination, which can lead to inbreeding depression in plants.



Such effects could ripple through ecosystems. Plants that rely on native bees for effective pollination may see lower reproduction rates. This could further degrade habitats that native bees and other wildlife depend on.



<h2 class="wp-block-heading" id="h-the-spread-of-feral-honey-bees">The spread of feral honey bees </h2>



Feral honey bee colonies are not just an issue in Southern California. These bees have spread worldwide and often outnumber managed colonies.



They thrive in many ecosystems and are difficult to remove once established. Unlike managed bees, feral colonies are self-sustaining and active year-round.



The study points out that feral honey bees have even replaced native bees in other regions. In the southwestern United States, they are increasingly common on both abundant and rare plants.



<h2 class="wp-block-heading" id="h-rethinking-conservation-priorities">Rethinking conservation priorities</h2>



Many people remain unaware of the negative effects of honey bees on native wildlife. Public concern tends to focus on protecting honey bees from disease and habitat loss.



Yet, the study’s authors warn that in North America, honey bees often act as competitors, not conservation targets.



“The plight of the honey bee is an issue of animal husbandry and livestock management, whereas when it comes to conservation issues here in North America, honey bees are likelier to be part of the problem, not a solution or a target for conservation,” said Hung.



This statement challenges common assumptions. It suggests a need for more balanced conservation strategies that consider native pollinators too.



<h2 class="wp-block-heading" id="h-steps-toward-potential-solutions">Steps toward potential solutions</h2>



Managing honey bee populations in sensitive areas may help. The researchers suggest limiting commercial beekeeping on public lands after crop blooms end.



“In areas with threatened bee species, natural preserve managers may also want to consider systematic removals or relocations of non-native honey bee colonies to provide wild bees a fighting chance,” said Hung.



Though such measures may seem extreme, they are not unprecedented. Many conservation programs already target invasive species to protect native wildlife.



<h2 class="wp-block-heading" id="h-honey-bees-harming-native-life">Honey bees harming native life</h2>



The study reveals a hidden layer of the pollination crisis. Honey bees, often seen as ecological heroes, can create serious problems in certain ecosystems.



As more people become aware of this issue, discussions around pollinator conservation may shift. Future efforts must balance the needs of agriculture with the importance of protecting native species.



The story of honey bees in Southern California serves as a reminder. Even well-known species can become a threat when removed from their native contexts.



Protecting biodiversity requires seeing the full picture, even when it challenges popular beliefs.



The study is published in the journal <a href="https://resjournals.onlinelibrary.wiley.com/doi/10.1111/icad.12858" target="_blank" rel="noreferrer noopener">Insect Conservation and Diversity</a>.



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Honey bee invasion: A growing threat to native pollinators

Pollinators are vital for the natural world. They help plants...

Coral reefs are in trouble. As oceans warm and environments shift, the vibrant ecosystems built by corals are turning pale and dying off. 



While scientists have known for years that coral bleaching is linked to the loss of symbiotic algae, they’ve never been able to watch the process unfold at the cellular level in realtime - until now.



<h2 class="wp-block-heading" id="h-underwater-microscope-for-studying-coral">Underwater microscope for studying coral</h2>



Researchers at the <a href="https://scripps.ucsd.edu/">Scripps Institution of Oceanography at UC San Diego</a> have created a handheld underwater microscope. The device makes it possible to study coral photosynthesis right where it happens - in the ocean, inside living coral tissue - without causing any damage.



The team named the device the Benthic Underwater Microscope imaging PAM - BUMP, for short.



The Jaffe Lab for Underwater Imaging at Scripps Oceanography built the microscope with support from the U.S. National Science Foundation.



The tool combines imaging with a light-based technique known as pulse amplitude modulated (PAM) fluorometry to measure how efficiently tiny algae inside corals are <a href="https://www.earth.com/news/the-fate-of-coral-reefs-lies-in-the-hands-of-their-tiny-inhabitants/">photosynthesizing</a>.



<h2 class="wp-block-heading" id="h-coral-depends-on-glowing-algae">Coral depends on glowing algae</h2>



The algae, called <a href="https://www.earth.com/news/symbiosis-will-help-some-corals-survive-in-a-warming-world/">symbionts</a>, are essential for coral survival. They live within coral tissue and convert sunlight, water, and carbon dioxide into sugars and oxygen.



The coral, in turn, uses that energy to grow and build reefs. But when stressed by warming seas or pollution, corals eject these algae. Without them, corals appear white and slowly starve - known as the bleaching effect.



The BUMP microscope makes it possible to monitor this relationship in real-time and in natural environments - something that couldn’t be done before.



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



“This microscope is a huge technological leap in the field of coral health assessment,” said study lead author Or Ben-Zvi, a postdoctoral researcher at Scripps Oceanography. 



“Coral reefs are rapidly declining, losing their photosynthetic symbiotic algae in the process known as <a href="https://www.earth.com/news/the-worlds-largest-coral-bleaching-event-is-now-underway/">coral bleaching</a>."



"We now have a tool that allows us to examine these microalgae within the coral tissue, noninvasively and in their natural environment.”



The microscope is small enough to fit in a carry-on suitcase. It’s light enough for a diver to bring to the seafloor without a ship’s help. 



Controlled with a touchscreen and powered by a battery pack, the microscope uses focused LED lights and high-magnification lenses to capture vivid images and videos. It also creates detailed 3D scans and maps photosynthesis in high resolution.



<h2 class="wp-block-heading" id="h-microscope-reveals-corals-inner-glow">Microscope reveals corals’ inner glow</h2>



At just 10 micrometers wide - one-tenth the width of a human hair - coral symbionts are invisible to the naked eye. But when corals are viewed under the microscope, the <a href="https://www.earth.com/news/marine-algae-genes-chlorophyll-boost-crop-yields-land-plants/">algae</a> glow red due to chlorophyll, the pigment that powers <a href="https://www.earth.com/news/key-to-life-on-earth-photosynthesis-begins-on-the-quantum-level-with-a-single-photon/">photosynthesis</a>. 



PAM technology measures this glow to calculate how efficiently the algae are converting light into energy. Other glowing areas, like cyan and green patches, come from fluorescent proteins that the coral produces, often around its mouth and tentacles. 



The images help researchers “see” coral health without touching or harming them. "We get a lot of information about their health without the need to interrupt nature,” said Ben-Zvi. 



“It's similar to a nurse who takes your pulse and tells you how well you're doing. We're checking the coral's pulse without giving them a shot or doing an intrusive procedure on them.”



<h2 class="wp-block-heading" id="h-observing-corals-at-unseen-scales">Observing corals at unseen scales</h2>



Ben-Zvi and her colleagues tested the microscope at coral hotspots around the world - including Hawaii, the Red Sea, and <a href="https://www.earth.com/news/coral-reefs-in-some-parts-of-the-world-actually-benefit-from-warming-el-nino-events/">Palmyra Atoll</a> - in collaboration with the Smith Lab at Scripps Oceanography. 



What they saw surprised them. Corals weren’t passive. They moved constantly, changing shape, reacting to particles, and even behaving in ways that looked like fighting or kissing.



Ben-Zvi observed coral polyps contracting their tentacles, possibly trying to remove or capture something floating by.



“The more time we spend with this microscope, the more we hope to learn about corals and why they do what they do under certain conditions,” she said. 



“We are visualizing photosynthesis, something that was previously unseen at the scales we are examining, and that feels like magic.”



<h2 class="wp-block-heading" id="h-early-detection-of-coral-stress">Early detection of coral stress</h2>



Corals face serious threats from climate change, and once bleaching begins, it can be hard to stop. But this microscope might help researchers catch problems earlier.



“The microscope facilitates previously unavailable, underwater observations of <a href="https://www.earth.com/news/what-grazing-halos-and-parrotfish-reveal-about-coral-reef-health/">coral health</a>, a breakthrough made possible thanks to the National Science Foundation and its critical investment in technology development,” said Jules Jaffe, a research oceanographer at Scripps and co-author of the study. 



Without continued federal funding, scientific research is at risk. In this case, however, support from <a href="https://www.nsf.gov/">NSF</a> enabled the team to build a device that helps solve the physiological mystery of coral bleaching and, ultimately, inform efforts to reverse it.



By detecting signs of stress before the coral reaches the tipping point, the researchers hope to create better strategies for protecting reefs from events like marine heatwaves.



<h2 class="wp-block-heading" id="h-studying-kelp-and-ocean-algae">Studying kelp and ocean algae</h2>



The potential doesn’t stop with corals. Scientists at Scripps Oceanography are already using the BUMP microscope to study other tiny marine life that rely on photosynthesis, including baby kelp off the coast of California.



“Since photosynthesis in the ocean is important for life on earth, a host of other applications are imaginable with this tool, including right here off the coast of San Diego,” said Jaffe.



In short, the BUMP microscope gives scientists something they’ve never had before: a new way to look at life underwater - close up, in motion, and alive. And with this new perspective, scientists are hoping to find better ways to protect some of the most fragile ecosystems on the planet.



The full study was published in the journal <a href="https://besjournals.onlinelibrary.wiley.com/doi/10.1111/2041-210X.70078">Methods in Ecology and Evolution</a>.



About the image: The photo features the coral&nbsp;Stylophora pistillata&nbsp;taken with the new micrsope, BUMP. Each polyp has a mouth and a set of tentacles, and the red dots are individual microalgae residing inside the coral tissue. Credit: Or Ben-Zvi



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Microscope reveals coral health in unprecedented detail

Coral reefs are in trouble. As oceans warm and environments...

Indian,Senior,Woman,Have,Sensitive,Teeth,With,Ice,Lolly,Or

For most of us, teeth mean crunching pretzels or tearing steak. But a new fossil analysis suggests their first job was feeling the world, not shredding it.



“What good is having all these teeth on the outside?” asked Yara Haridy of the <a href="https://www.uchicago.edu/en" target="_blank" rel="noreferrer noopener">University of Chicago</a>, lead author of the study. Using high‑energy scans, researchers found that the earliest tooth‑like bumps sat on fish skin and were wired for sensation.&nbsp;



<h2 class="wp-block-heading" id="h-teeth-began-as-skin-sensors">Teeth began as skin sensors</h2>



These skin teeth, known as <a href="https://www.morphosource.org/projects/000626244" target="_blank" rel="noreferrer noopener">odontode units</a>, appear in Eriptychius fossils from the middle <a href="https://ucmp.berkeley.edu/ordovician/ordovician.php" target="_blank" rel="noreferrer noopener">Ordovician Period</a>, roughly 460 million years ago. 



Slicing the fossils reveals thick bands of <a href="https://www.drbicuspid.com/clinical/imaging-cad-cam/article/15747523/fossil-scans-of-ancient-fish-may-explain-modernday-tooth-sensitivity" target="_blank" rel="noreferrer noopener">dentine</a>, the same pain‑transmitting material that still lies beneath human enamel.



Each odontode contains a pulp <a href="https://www.earth.com/news/tooth-enamel-analysis-suggests-early-eurasians-were-multiple-species-paranthropus-robustus/">cavity</a> and wide tubules that open at the surface, a layout ideal for detecting pressure or temperature shifts. By contrast, later fish with heavy enamel caps muted that sensitivity but gained better protection.



One celebrated Cambrian candidate for the “first fish,” Anatolepis, has been demoted after fresh scans showed its bumps match arthropod <a href="https://abc7chicago.com/post/university-chicago-study-finds-tooth-sensitivity-may-linked-ancient-fish-led-dr-yara-haridy/16499129/" target="_blank" rel="noreferrer noopener">sensilla</a>, not vertebrate dentine.



<h2 class="wp-block-heading" id="h-early-armor-came-with-nerves">Early armor came with nerves</h2>



Sensilla in crabs and scorpions let them taste, feel vibration, and track currents. Early vertebrates adopted a similar strategy, embedding nerves inside mineral caps that hardened into armor.



“Tooth‑like structures likely first evolved in the skin of early vertebrates, prior to the oral invasion of these structures that became teeth,” said <a href="https://biology.ufl.edu/gareth-fraser/" target="_blank" rel="noreferrer noopener">Gareth Fraser</a> of the University of Florida, an evolutionary biologist not involved in the scans.



Because armor muffles most tactile cues, adding built‑in sensors restored environmental awareness without sacrificing defense. The same compromise appears again and again whenever <a href="https://www.earth.com/news/scientists-finally-confirm-species-identity-of-the-dragon-man-fossil-skull-denisovan/">animals</a> grow shells, scales, or plates.



The Ordovician seas teemed with cephalopods and sea scorpions, so feeling a predator brush past could mark the difference between survival and lunch. Even a thin sensory layer offered that edge.



<h2 class="wp-block-heading" id="h-teeth-moved-from-skin-to-mouth">Teeth moved from skin to mouth</h2>



Once fish started lunging at prey, bringing those hard nodules inside the oral cavity made practical sense. The genetic toolkit for building odontodes simply redeployed along the jaw line.



CT reconstructions show a stepwise shift, first lining lips, then clustering on internal ridges that became true teeth. No new tissue was required, only a new address.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/human-teeth-sensitivity_evolution_skate-fish_CT-scan_tooth-like-denticles_Yara-Haridy_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/human-teeth-sensitivity_evolution_skate-fish_CT-scan_tooth-like-denticles_Yara-Haridy_1s.webp" alt="CT scan of the front of a skate, showing the hard, tooth-like denticles (orange) on its skin. Yara Haridy" class="wp-image-1976721"/></a><figcaption class="wp-element-caption">CT scan of the front of a skate, showing the hard, tooth-like denticles (orange) on its skin. Click image to enlarge. Credit: Yara Haridy</figcaption></figure>



This migration explains why modern teeth still flinch when chilled soda hits exposed dentine. The tissue did not lose its ancient job, even after millions of years chewing. 



Human <a href="https://pubmed.ncbi.nlm.nih.gov/21168271/" target="_blank" rel="noreferrer noopener">odontoblast cells</a> inside dentine express <a href="https://www.ncbi.nlm.nih.gov/books/NBK5244/" target="_blank" rel="noreferrer noopener">temperature‑sensing TRP channels</a> that trigger pain signals, reinforcing the link between sensation and tooth structure.



<h2 class="wp-block-heading" id="h-ice-cream-pain-is-ancient">Ice cream pain is ancient</h2>



Skates, sharks, and certain catfish still wear odontodes across their skin, and fluorescent imaging reveals nerves curling around each unit. The same wiring lights up in their oral teeth.



Dentists encounter the legacy daily: about 30 percent of adults report <a href="https://pubmed.ncbi.nlm.nih.gov/34302871/" target="_blank" rel="noreferrer noopener">dentin hypersensitivity</a> - a direct outcome of open tubules harking back to those armored swimmers.



Laboratory studies show that activating <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC4541108/" target="_blank" rel="noreferrer noopener">TRPA1 and TRPV4</a> channels in human odontoblasts releases ATP, a chemical that excites nearby nerves and sparks the familiar zing of ice‑cream pain.



Understanding the fossil record clarifies why blocking tubules with varnishes or bioactive glasses calms sensitivity more reliably than numbing gels alone. Closing the ancient sensory windows cuts the signal at its source.



<h2 class="wp-block-heading" id="h-fossil-mistake-changed-tooth-history">Fossil mistake changed tooth history</h2>



The misidentification of Anatolepis as a vertebrate with dentine pushed the timeline of true teeth further back than the evidence supports. 



With updated scans showing Anatolepis as an arthropod, the emergence of real vertebrate dental tissue now firmly begins in the middle Ordovician.



This correction removes about 40 million years of assumed vertebrate history. It also reorients where scientists search for the evolutionary leap from external skin sensors to internal biting tools.



<h2 class="wp-block-heading" id="h-ancient-teeth-link-to-modern-health">Ancient teeth link to modern health</h2>



Reclassifying Anatolepis as an <a href="https://www.earth.com/news/cambrian-fossils-reveal-new-clues-about-arthropod-evolution/">arthropod</a> pushes the oldest confirmed vertebrate dentine forward by almost 40 million years, tightening the evolutionary timeline. Paleontologists can now focus on <a href="https://www.earth.com/news/470-million-year-old-animal-fossils-discovered-in-frances-cabrieres-biota/">Ordovician</a> strata when hunting the first mouths with teeth.



The fossil findings also challenge textbook diagrams that present teeth as novel structures formed deep inside the jaw. 



Instead, they appear as immigrants from the skin, carrying sensory baggage that still shapes dental health.



Medical researchers already mine shark and skate genes to inspire regenerative dentistry. Knowing those genes once built skin sensors may guide efforts to coax human cells into growing replacement enamel.



Finally, the study highlights a broader pattern: nature often solves different problems with the same parts. 



Sensory armor, lateral‑line canals, and even mammal whiskers show how sensation sneaks into protective structures whenever the need arises.



The study is published in <a href="https://www.nature.com/articles/s41586-025-08944-w" target="_blank" rel="noreferrer noopener">Nature</a>.



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Fossil discovery explains why our teeth are still so sensitive to cold

For most of us, teeth mean crunching pretzels or tearing...

Earth’s earliest complex organisms endured harsh environments, and a new study reveals how these ancient life forms used arsenic to survive.



Researchers studied 2.1-billion-year-old fossils from Gabon’s Francevillian Basin. These fossils belong to eukaryotes, <a href="https://www.earth.com/news/tiny-microbes-may-have-given-rise-to-complex-life/">organisms</a> with advanced cells.



The team found that these ancient organisms stored arsenic inside special cell compartments. This strategy helped them survive in seas with even low arsenic levels.



Using advanced X-ray technology, they mapped arsenic inside of the fossils. The analysis revealed that arsenic was not the result of later contamination. Instead, it was locked inside during the organisms’ lives.



<h2 class="wp-block-heading" id="h-ancient-seas-triggered-arsenic-defenses">Ancient seas triggered arsenic defenses</h2>



The study offers a fresh view of early <a href="https://www.earth.com/news/world-turtle-day-2025-ancient-creatures-with-modern-challenges/">life</a>’s fight against toxins. The fossils lived in oxygen-rich seas with plenty of phosphate. However, even in these waters, arsenate - the toxic form of arsenic - posed a problem.



“The ability to cope with arsenic was not something eukaryotes developed randomly,” explained Dr. Ernest Chi Fru from <a href="https://www.cardiff.ac.uk" target="_blank" rel="noreferrer noopener">Cardiff University</a>.



During this period, Earth’s oxygen levels began to rise. This change made arsenate more common. Since arsenate closely resembles phosphate, it easily entered cells.



Organisms faced a tough challenge. They needed ways to avoid poisoning while still absorbing phosphate, a nutrient essential for life.



<h2 class="wp-block-heading" id="h-fossils-show-arsenic-stored-in-bodies">Fossils show arsenic stored in bodies</h2>



The fossils showed high arsenic concentrations, far above the levels in surrounding rocks. This suggests they absorbed arsenic during their lifetime.



X-ray imaging revealed arsenic at the core of tiny pyrite crystals inside the <a href="https://www.earth.com/news/cambrian-explosion-fossils-push-back-the-rise-of-complex-life/">fossils</a>. This points to a biological origin. The arsenic likely came from within the organisms, not from the environment after burial.



Other structures in the same rocks did not show such patterns. Abiotic concretions nearby lacked this arsenic core structure. Similar arsenic-rich patterns appear in some younger animal fossils. However, they are absent in purely mineral samples.



This difference suggests that the Francevillian organisms actively stored arsenic. It wasn’t simply absorbed from surrounding waters after death.



<h2 class="wp-block-heading" id="h-arsenic-storage-for-survival">Arsenic storage for survival</h2>



The researchers tested three scenarios to explain arsenic in the <a href="https://www.earth.com/news/why-we-see-some-animals-as-more-human-than-others/">fossils</a>. First, they ruled out passive absorption from decaying organic material. 



Second, the team dismissed the idea that sulfate-reducing microbes introduced the arsenic. The most likely explanation was bioaccumulation. These organisms absorbed arsenic during their lifetime and stored it inside their bodies.



“This suggests a pronounced biogenic control on arsenic storage,” wrote the researchers. They argue that arsenic storage was not just a survival trick. It was an adaptation tied to the rise of oxygen in Earth’s oceans.



<h2 class="wp-block-heading" id="h-arsenic-damaged-ancient-life-systems">Arsenic damaged ancient life systems</h2>



Arsenic disrupts life by mimicking phosphate. Once inside cells, it blocks key processes like energy production and genetic functions.



Modern organisms use efflux pumps or special enzymes to remove arsenic. Some even store it safely in vacuoles or vesicles.



The fossils showed traces of arsenic linked with other metals like nickel and copper. These metals can also be toxic in high amounts.



This suggests the organisms had a broader detoxification system. They may have stored multiple harmful elements together.



<h2 class="wp-block-heading" id="h-modern-sponges-use-similar-storage">Modern sponges use similar storage</h2>



The researchers drew comparisons with modern sponges. These ancient animals often store arsenic in special compartments.



Sponges use this strategy because it helps them manage metal exposure from their filter-feeding lifestyle.



The Francevillian organisms might have done something similar. Their environment had low arsenic levels, but long-term exposure likely led to gradual buildup inside their bodies.



The stored arsenic later formed pyrite crystals during fossilization. The researchers’ model shows how this process left clear chemical markers in the fossils.



<h2 class="wp-block-heading" id="h-the-evolution-of-complex-life">The evolution of complex life</h2>



The findings suggest that arsenic detoxification emerged very early in the evolution of eukaryotic life. It was likely not a rare or isolated event. 



Instead, the ability to manage arsenic probably evolved multiple times throughout Earth’s long history, as different organisms adapted to shifting environmental conditions.



These arsenic-rich fossils reveal much more than just details about ancient organisms. They serve as powerful tools for researchers, offering a way to detect signs of early life in rocks that are billions of years old. 



The chemical traces left behind provide strong clues about how life evolved and adapted in hostile environments.



<h2 class="wp-block-heading" id="h-survival-strategies-of-ancient-life">Survival strategies of ancient life</h2>



Ultimately, the research highlights the importance of chemical signatures as records of biological processes. 



Even when organic material disappears, these chemical patterns can tell the story of ancient survival strategies and environmental challenges.



By storing arsenic within their cells, these early organisms developed a unique way to survive in toxic seas. In doing so, they not only overcame dangerous conditions but also preserved a chemical fingerprint that allows scientists today to uncover their ancient existence.



The study is published in the journal <a href="https://www.nature.com/articles/s41467-025-59760-9" target="_blank" rel="noreferrer noopener">Nature Communications</a>.



Image Credit: Arnaud Mazurier and Abderrazak El Albani



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Why ancient organisms stored arsenic inside their cells

Earth’s earliest complex organisms endured harsh environments, and a new...

When researchers lowered a cow carcass 5,345 feet (1,629 meters) beneath the waves off Hainan Island, they were studying natural whale fall processes in the deep sea. Instead, the bait attracted uninvited guests never before filmed in these waters: Pacific sleeper sharks (Somniosus pacificus).



The video, captured on the continental slope of the northern South China Sea, marks the species’ southernmost sighting in the Pacific Basin. 



It also reveals a suite of behaviors - from polite feeding queues to protective eye retractions - that deepen our understanding of how large predators survive in the deep ocean.



<h2 class="wp-block-heading" id="h-sharks-spotted-far-from-home">Sharks spotted far from home</h2>



Until now, Pacific sleeper sharks were considered residents of the North Pacific, with records stretching from Japan and the <a href="https://www.earth.com/news/why-did-billions-of-crabs-vanish-from-the-bering-sea/">Bering Sea</a> to Alaska and as far south as Baja California. Their sudden appearance in tropical latitudes stunned marine biologists.



The deployment, designed to mimic a natural whale fall, quickly drew multiple sharks that took turns tearing at the carcass. 



Because sleeper sharks routinely dive below 3,280 feet (1,000 meters), direct observations have been scarce. Remote baited cameras provided the first clear window into their deep-sea routines.



<h2 class="wp-block-heading" id="h-size-shapes-shark-feeding-style">Size shapes shark feeding style</h2>



Back on shore, the research team reviewed hours of footage and divided the sharks into two categories: individuals longer than 8.85 feet (2.7 meters) and those shorter. 



The threshold was chosen purely as a reference point, not as a marker of maturity.



<a href="https://www.earth.com/news/how-the-sharks-body-grows-with-geometric-precision/">Size</a> proved to be a major factor in feeding style. The bigger sharks charged the carcass head-on, ripping chunks of flesh with sweeping bites. Smaller sharks kept their distance, circling watchfully before making tentative nips. 



The contrast suggests a competitive hierarchy in which bulk confers priority access to limited resources.



<h2 class="wp-block-heading" id="h-sharks-take-polite-turns">Sharks take polite turns</h2>



Perhaps the most unexpected behavior was a kind of underwater etiquette. As each shark finished feeding, it glided away, making room for the next arrival. 



<a href="https://spj.science.org/doi/10.34133/olar.0095" target="_blank" rel="noreferrer noopener">On the video camera footage</a>, the handover looked almost orderly, with newcomers approaching steadily from behind while current feeders yielded position.



“This behavior suggests that feeding priority is determined by individual competitive intensity, even in deep-water environments," said study author Han Tian, a marine biologist at <a href="https://www.sysu.edu.cn/sysuen/">Sun Yat-sen University</a>. 



"This reflects a survival strategy suitable for non-solitary foraging among Pacific sleeper sharks.”



Comparable line-ups have been reported when sharks scavenge floating whale carcasses near the surface, where space is equally contested. 



The deep-sea footage indicates that such social rules persist even in the aphotic zone, where encounters are rare and every calorie counts.



<h2 class="wp-block-heading" id="h-defensive-eye-roll"><a></a>Defensive eye roll</h2>



Pacific sleeper sharks lack the nictitating membrane - a transparent eyelid - found in many shark species. Yet the video shows them repeatedly retracting their eyes while feeding.



Scientists interpret this as a built-in safeguard against sudden jabs from protruding bones or the teeth of rival sharks. 



The involuntary eye roll could compensate for the missing membrane, protecting vision during frenzied meals.



<h2 class="wp-block-heading" id="h-clues-to-an-expanded-range"><a></a>Clues to an expanded range</h2>



Finding Pacific sleeper sharks 1,800 miles (3,000 kilometers) south of their documented range forces scientists to rethink what governs their distribution. 



Do shifting <a href="https://www.earth.com/news/ocean-temperatures-are-rising-faster-than-expected-and-likely-to-accelerate/">ocean temperatures</a> invite them farther into the tropics? Or does the South China Sea offer prey reservoirs that make the journey worthwhile?



All individuals filmed were female - a pattern echoed by other rarely seen giants such as the megamouth shark, which also shows a female bias here. 



The sex skew hints that the region might double as a nursery or feeding ground for pregnant sharks needing high-energy meals.



<h2 class="wp-block-heading" id="h-energy-in-the-abyss">Energy in the abyss</h2>



Large predators cannot thrive without a steady food supply. Sleeper sharks typically scavenge or ambush seals and squids in colder waters.



In the subtropical South China Sea, their presence implies robust nutrient pathways moving organic matter from surface ecosystems to abyssal depths.



<figure class="wp-block-image aligncenter size-full"><a href="https://spj.science.org/doi/10.34133/olar.0095" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/07/pacific-sleeper-sharks_rare-observations_deep-ocean_SME-DEEP_1s.webp" alt="The presence of Pacific sleeper sharks of varying body sizes was detected in the deep waters of the South China Sea using stationary cameras, with all individuals identified as female. Credit: Ocean-Land-Atmosphere Research" class="wp-image-1976702"/></a><figcaption class="wp-element-caption">The presence of Pacific sleeper sharks of varying body sizes was detected in the deep waters of the South China Sea using stationary cameras, with all individuals identified as female. Click image to watch the video. Credit: Ocean-Land-Atmosphere Research</figcaption></figure>



“The highly aggressive behavior of sharks observed in the South China Sea suggests that this region still harbors abundant food sources in the deep sea," Tan said. 



"But what exactly are they? This question is intriguing for both animal distribution and behavioral research.”



<h2 class="wp-block-heading" id="h-tracking-sharks-in-the-deep">Tracking sharks in the deep</h2>



The team plans to deploy additional baited cameras and <a href="https://www.earth.com/news/dna-fishing-helps-scientists-survey-marine-life-in-the-deep-ocean/">environmental DNA</a> samplers across the basin to gauge how many Pacific sleeper sharks prowl these depths and whether they stay year-round. 



Comparative studies from other oceans could reveal whether deep-water queuing is widespread among large scavengers or unique to this lineage.



Biologists also hope to determine if <a href="https://www.earth.com/news/danger-zones-climate-change-is-altering-predator-prey-dynamics/">climatic changes</a> or altered current patterns are drawing cold-adapted predators southward. 



Answers will feed into global models of deep-sea energy flow and illuminate how carbon moves from surface waters to the seafloor, a key piece of the climate puzzle.



For now, the footage shatters old assumptions. Pacific sleeper sharks are not confined to polar and subpolar seas. 



They form loose social hierarchies, even in perpetual darkness, and they may rely on uncharted nutrient highways that link surface productivity with the deep ocean.



-----



<a href="https://spj.science.org/doi/10.34133/olar.0095" target="_blank" rel="noreferrer noopener">Click here to watch the full video footage...</a>



The study is published in the journal <a href="https://spj.science.org/doi/10.34133/olar.0095" target="_blank" rel="noreferrer noopener">Ocean-Land-Atmosphere Research</a>.



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Rare video shows elusive deep-sea predators feeding thousands of miles from home

When researchers lowered a cow carcass 5,345 feet (1,629 meters)...

Greenland sharks cruise the North Atlantic at a pace slower than most people walk, yet some were already adults when the United States was founded. 



Their astonishing lifespan has turned this elusive fish into a living time capsule, capturing the imagination of biologists and longevity researchers alike.



Julius Nielsen of the <a href="https://www.ku.dk/en" target="_blank" rel="noreferrer noopener">University of Copenhagen</a> leads many of the modern expeditions that tag, scan, and sometimes briefly corral these giants in the icy dark.



<h2 class="wp-block-heading" id="h-why-greenland-sharks-live-so-long">Why Greenland sharks live so long</h2>



<a href="https://www.science.org/doi/10.1126/science.aaf1703" target="_blank" rel="noreferrer noopener">Eye‑lens radiocarbon dating</a> shows females can live at least 272 years, with one specimen estimated at 392 ± 120 years. The method pinpoints birth dates because the lens proteins stop exchanging carbon after a shark pup forms in utero.



“This is the longest living vertebrate that we know of,” said Nielsen, who helped age the record fish. He and colleagues calculate that females do not reach sexual maturity until roughly 150 years, a timetable unheard of in other sharks.



Slow annual growth, barely half an inch, means injuries heal gradually but bones and organs escape the cumulative cellular wear seen in faster‑growing <a href="https://www.earth.com/news/shark-skeletons-could-lead-to-technological-innovations/">animals</a>. 



Researchers suspect a combination of frigid water, low oxygen demand, and genes that police DNA damage all contribute, yet no single “silver bullet” for longevity has appeared.



<h2 class="wp-block-heading" id="h-greenland-sharks-have-slow-heartbeats">Greenland sharks have slow heartbeats</h2>



Greenland sharks have resting <a href="https://journals.biologists.com/jeb/article/221/19/jeb186957/33812" target="_blank" rel="noreferrer noopener">heart rates</a> of about 10 beats per minute and unusually low blood pressure. That’s much lower than what you’d find in other large sharks, and it may help protect their blood vessels from long-term damage like heart attacks or strokes.



Even with such a slow heartbeat, each pump moves a lot of blood, keeping their <a href="https://www.earth.com/news/different-shark-species-seen-scavenge-feeding-together-in-rare-event/">bodies</a> fueled during slow swimming under Arctic ice. 



Doctors are paying attention, hoping this natural “strong pump, gentle pressure” system could offer ideas for treating high blood pressure in people.



<h2 class="wp-block-heading" id="h-slow-bodies-save-energy">Slow bodies save energy</h2>



These sharks burn energy very slowly. In fact, their oxygen use is among the <a href="https://www.nature.com/articles/s41598-020-76371-0" target="_blank" rel="noreferrer noopener">lowest ever recorded</a> for a fish their size. That kind of slow metabolism may reduce cell damage over time and help them survive long gaps between meals. 



A 280-pound shark might get through the day on fewer calories than a cheeseburger, making a single big meal last for months.



Because the deep Arctic is so cold, they digest food slowly too. Instead of burning energy for speed or growth, they stretch it out for <a href="https://www.earth.com/news/mediterranean-sharks-face-growing-threats-despite-conservation-efforts/">survival</a>.



<h2 class="wp-block-heading" id="h-why-they-are-toxic-top-predators">Why they are toxic top predators</h2>



Greenland shark meat is laced with <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC5127123/" target="_blank" rel="noreferrer noopener">trimethylamine N‑oxide</a>, a compound that stabilizes proteins under high pressure yet renders the raw flesh neurotoxic to mammals.



Icelanders neutralize it through months of fermentation to create the ceremonial dish kæstur hákarl, but few tourists finish more than a nibble.



The species ranks as an apex predator; evidence shows adults seizing fish, squid, and the occasional sleeping seal. 



Sightings in the Gulf of Mexico and off Spain reveal a wider range than once believed, hinting at deep‑water corridors that connect polar and temperate seas.



<h2 class="wp-block-heading" id="h-greenland-sharks-are-at-risk">Greenland sharks are at risk</h2>



Commercial trawlers unintentionally haul up about 3,500 Greenland <a href="https://www.forbes.com/sites/melissacristinamarquez/2022/11/07/greenland-shark-finally-gets-protection/" target="_blank" rel="noreferrer noopener">sharks</a> each year as bycatch. Because breeding may not begin for a century and a half, losing even sub‑adults chips away at population recovery.



The <a href="https://www.iucnredlist.org/species/60213/3112909" target="_blank" rel="noreferrer noopener">International Union for Conservation of Nature</a> lists the species as “Vulnerable,” citing low fecundity and expanding deep‑sea fisheries. 



Simple changes, switching to LED‑lit nets that deter sharks, banning deep set gill nets in nursery zones, and funding release‑training for crews, can cut mortality without shrinking catches of cod or halibut.



Scientists also urge Arctic nations to establish no‑take refuges around known mating aggregations once those secret sites are found. Protecting a fish that may still be swimming in 2425 demands policies that look far beyond typical political horizons.



<h2 class="wp-block-heading" id="h-the-search-for-hidden-nursery-grounds">The search for hidden nursery grounds</h2>



No one has ever observed Greenland sharks mating or giving birth in the wild. Only one pregnant female has been studied, and her embryos suggest the species may be <a href="https://www.fisheries.noaa.gov/feature-story/sharpen-your-shark-facts" target="_blank" rel="noreferrer noopener">aplacental viviparous</a>, meaning the young develop inside eggs that hatch within the mother’s body.



Females seem to carry up to 10 pups at a time, but the <a href="https://www.fisheries.noaa.gov/feature-story/five-wild-facts-about-shark-reproduction" target="_blank" rel="noreferrer noopener">gestation period</a> could last several years. Without regular breeding or nursery sightings, it's hard to estimate how often they reproduce or whether their range shifts during these vulnerable periods.



This gap in knowledge makes population modeling difficult. Without better data, scientists can't say how quickly these sharks could recover if current bycatch trends continue. 



Tagging mature females may help reveal mating routes or hidden nursery grounds. Learning how and where they reproduce could play a key role in designing effective marine protected areas.



The study is published in the journal <a href="https://www.science.org/doi/10.1126/science.aaf1703" target="_blank" rel="noreferrer noopener">Science</a>.



Image Credit: Julius Nielsen



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Longest-living vertebrates on Earth survive for centuries in icy waters

Greenland sharks cruise the North Atlantic at a pace slower...

Bumble bees, like humans, sometimes eat the wrong things. A new study shows they may pick foods that don’t meet their nutritional needs - and those choices might actually harm their health.



In research conducted at <a href="https://www.psu.edu/">Penn State University</a>, scientists found that when bumble bees were offered diets enriched with varying levels of protein, fat, and carbohydrates, their eating habits didn’t lead to better health. 



The study raises new questions about how bees choose what to eat - and whether those choices are good for them.



<h2 class="wp-block-heading" id="h-bumble-bees-don-t-choose-healthy-options">Bumble bees don't choose healthy options</h2>



The researchers designed a controlled study where bumble bees were split into groups and given specific diets. Some groups received <a href="https://www.earth.com/news/bee-survival-depends-on-more-than-just-pollen-abundance/">pollen</a> with added protein or fat. Others got nectar-like sugar solutions with different sugar levels. 



A control group was allowed to eat a standard diet of wild pollen and a 60% sugar solution. All the bees were the same age and housed in small groups to keep testing conditions consistent. 



What happened next surprised the researchers. The bumble bees didn't go for the food options that were healthy. 



The bees ate more when protein levels in pollen were higher, less when fat levels were higher, and they over-consumed sugar when the nectar was watered down. 



None of the eating patterns benefited the physical health of the bumble bees. Egg-laying declined. Body weight stayed the same or dropped. Nothing the bees chose to eat led to better outcomes than the control group.



<h2 class="wp-block-heading" id="h-bumble-bees-make-bad-food-choices">Bumble bees make bad food choices</h2>



The results challenge the long-standing assumption that bees instinctively know what to eat to stay healthy.



Etya Amsalem is an associate professor of entomology in the College of Agricultural Sciences and lead author of the study. She noted that bee preferences are unlikely to reflect true needs and more likely result from evolutionary constraints.



“For instance, bees may under-consume lipids not because high-lipid diets are harmful, but because their physiology is not well-suited for digesting or storing large amounts of lipids," said Professor Amsalem.



“Bees may over-consume proteins because they have evolved to seek them out whenever they’re available, even though excess protein can be detrimental because it affects how efficiently bees can eliminate nitrogen from their bodies."



This mismatch - between what bees eat and what actually helps them - may be putting more strain on already vulnerable bee populations.



<h2 class="wp-block-heading" id="h-why-this-matters-for-bee-survival">Why this matters for bee survival</h2>



Bumble bees are under serious stress worldwide. Habitat loss, <a href="https://www.earth.com/news/pesticides-attack-bees-in-multiple-ways-throughout-the-body/">pesticide</a> exposure, climate change, and industrial farming have drastically reduced the variety and quality of flowers bees depend on. 



In many areas, rich, diverse meadows have been replaced by monocultures or urban development. That leaves bees with fewer options - and often with subpar food sources.



This drop in floral diversity doesn’t just mean less food overall - it means less nutritionally balanced food. Even when bees find enough to eat, the quality of that food may not support key functions like reproduction, colony growth, or immune strength.



Nutrition plays a big role in <a href="https://www.earth.com/news/organic-farming-and-flower-strips-improve-honey-bee-health/">bee health</a>. But if bees can’t always tell what’s good for them, that complicates conservation efforts.



“It’s an odd assumption when you think about it - my toddler prefers chocolate over broccoli, but I wouldn’t conclude from that that chocolate is healthier for her,” said Professor Amsalem. 



“So, why do we assume bees are different? Understanding potential mismatches between consumption and fitness outcomes is important, as most conservation and management strategies assume bees can self-regulate their diets for optimal health.”



<h2 class="wp-block-heading" id="h-rethinking-bumble-bee-health">Rethinking bumble bee health</h2>



The results suggest that preference alone isn’t a reliable guide for diet planning - not for bees, and likely not for conservation strategies either. 



Instead of assuming bees will naturally eat what’s best for them, the researchers say we need a deeper understanding of how diet affects their health at a physiological level. According to Professor Amsalem, future research needs to dig deeper.



“Future research could investigate why bees fail to optimize diet - for example, metabolic limitations, gustatory biases or ecological tradeoffs - and may explore nonmacronutrient components like vitamins and minerals that may explain fitness discrepancies,” she said.



For conservation groups, farmers, and scientists trying to support healthy bee populations, this study is a clear reminder: what bees choose to eat may not be what’s best for them. And that makes understanding their real nutritional needs more urgent than ever.



The full study was published in the journal <a href="https://linkinghub.elsevier.com/retrieve/pii/S0022191025000769">Journal of Insect Physiology</a>.



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How bumble bees are sabotaging their own health

Bumble bees, like humans, sometimes eat the wrong things. A...

Off the eastern tip of Java, dredging barges dragged up more than sand. They pulled a piece of the past: a submerged river valley under the Madura Strait packed with fossils that had slept under fifty feet of water since long before the last Ice Age melted away.



Among the finds were two skull fragments of Homo erectus, a <a href="https://www.earth.com/news/fossil-discovery-anadoluvius-turkae-suggests-humans-originated-in-europe-not-africa/">human ancestor</a> that roamed Asia until roughly 117,000 years ago, as well as more than 6,000 animal fossils that paint a vivid portrait of a lost ecosystem. <a href="https://www.universiteitleiden.nl/en/staffmembers/harry-berghuis" target="_blank" rel="noreferrer noopener">Harold Berghuis</a> of <a href="https://www.universiteitleiden.nl/en" target="_blank" rel="noreferrer noopener">Leiden University</a> leads the team studying the haul.



<h2 class="wp-block-heading" id="h-sundaland-rises-then-sinks">Sundaland rises then sinks</h2>



During colder glacial times, much of Southeast Asia’s continental shelf formed a single low‑lying continent known as <a href="https://www.cepf.net/our-work/biodiversity-hotspots/sundaland#:~:text=The%20Sundaland%20Biodiversity%20Hotspot%20covers,islands%20of%20Borneo%20and%20Sumatra." target="_blank" rel="noreferrer noopener">Sundaland</a>. 



Sea level then sat about 400 feet lower than it does today, exposing wide plains crisscrossed by rivers and grasslands.



When global ice melted between <a href="https://www.nature.com/articles/s42003-023-04510-0" target="_blank" rel="noreferrer noopener">22,000 and 6,000 years ago</a>, the ocean climbed roughly 443 feet, drowning half of that landmass. 



The rapid pulses of rise carved islands out of peninsulas and pushed coastlines hundreds of miles inland, isolating plants, animals, and the people who depended on them.



Geologists can still follow the drowned river channels with high‑resolution sonar. Each channel marks a corridor that once connected Borneo, Sumatra, and Java to the Asian mainland, providing migration routes for both megafauna and hominins.



<h2 class="wp-block-heading" id="h-river-fossils-under-the-madura-strait">River fossils under the Madura Strait</h2>



The valley now mapped under the Madura Strait was carved by the ancient Solo River. 



Optically Stimulated Luminescence dating (<a href="https://www.antarcticglaciers.org/glacial-geology/dating-glacial-sediments-2/optically-stimulated-luminescence/" target="_blank" rel="noreferrer noopener">OSL</a>) shows its sandy fill settled between 162,000 and 119,000 years ago, anchoring the new fossils to the late <a href="https://www.sciencedirect.com/science/article/pii/S295023652500012X" target="_blank" rel="noreferrer noopener">Pleistocene</a>.



OSL works because quartz grains store energy from cosmic rays like tiny batteries. When technicians shine a laser on a grain in the lab, it releases that stored charge as light, revealing the moment the grain last basked in sunlight.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/madura-strait_sunda-shelf_homo-erectus-remains_map_credit-ScienceDirect_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/madura-strait_sunda-shelf_homo-erectus-remains_map_credit-ScienceDirect_1s.webp" alt="The Sunda Shelf of Southeast Asia, with the Indonesian archipelago. Box indicates the position of map B. B: Eastern Java, the Madura Strait, the Solo River, Ngandong, Sambungmacan, and other hominin sites. Box indicates the position of map C. C: The Madura Strait north of Surabaya, with the sand extraction area and the location of the BMS land-reclamation. Map data: GEBCO and ALOS" class="wp-image-1976530"/></a><figcaption class="wp-element-caption">The Sunda Shelf of Southeast Asia, with the Indonesian archipelago. Box indicates the position of map B. B: Eastern Java, the Madura Strait fossils location, the Solo River, Ngandong, Sambungmacan, and other hominin sites. Box indicates the position of map C. C: The Madura Strait north of Surabaya, with the sand extraction area and the location of the BMS land-reclamation. Click image to enlarge. Map data: GEBCO and ALOS</figcaption></figure>



The method is ideal for underwater sites where radiocarbon fails, yet it is rarely applied because retrieving uncontaminated samples from the seafloor is difficult. 



The Madura team’s success shows how pipeline spoil, often discarded as waste, can become forensic evidence on continental‑scale change.



<h2 class="wp-block-heading" id="h-madura-strait-reveals-fossil-menagerie">Madura Strait reveals fossil menagerie</h2>



The tally of species rivals a natural‑history museum catalog. There were buffalo, several kinds of deer, and <a href="https://nationalzoo.si.edu/animals/komodo-dragon" target="_blank" rel="noreferrer noopener">Komodo dragons</a> longer than a canoe.



The biggest draw, though, is <a href="https://eartharchives.org/articles/stegodon-the-elephant-with-sideways-trunk/index.html" target="_blank" rel="noreferrer noopener">Stegodon trigonocephalus</a>, an elephant‑like giant that could stand almost 13 feet at the shoulder. 



Its presence suggests tall grass and open water holes, conditions that match pollen studies from upland Java.



Fossil monitors link today’s dragon‑patrolled islands to their mainland roots; remains of <a href="https://ielc.libguides.com/sdzg/factsheets/komododragon" target="_blank" rel="noreferrer noopener">Varanus komodoensis</a> have turned up on nearby <a href="https://www.theextinctions.com/articles-1/lesser-sunda-islands-part-1-flores-and-sumba" target="_blank" rel="noreferrer noopener">Flores and Sumba</a>, confirming that the apex lizard once ranged far beyond its present refuges. 



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/maduro-strait_indonesia_homo-erectus_ancient-remains_credit-ScienceDirect_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/maduro-strait_indonesia_homo-erectus_ancient-remains_credit-ScienceDirect_1s.webp" alt="Madura Strait 1 (MS1): Homo erectus frontal fragment with dextral supraorbital torus. A: Photographs. B: CT-based 3D surface rendered images. Note that the exact orientation of the fragment is unknown. For the anterior view, a slightly diagonal orientation has been assumed. C: CT-based 3D surface rendered image of MS1 in a more horizontal orientation, with anatomical indications. D: CT-slice. Credit: ScienceDirect" class="wp-image-1976532"/></a><figcaption class="wp-element-caption">Madura Strait 1 (MS1) fossils: Homo erectus frontal fragment with dextral supraorbital torus. A: Photographs. B: CT-based 3D surface rendered images. Note that the exact orientation of the fragment is unknown. For the anterior view, a slightly diagonal orientation has been assumed. C: CT-based 3D surface rendered image of MS1 in a more horizontal orientation, with anatomical indications. D: CT-slice. Click image to enlarge. Credit: ScienceDirect</figcaption></figure>



Carnivore teeth in the assemblage are scarce, hinting that reptiles, not big cats, topped the food chain.



Antelope‑like bovids and open‑country rodents round out the scene, pointing to savanna rather than rainforest. Together the bones sketch a community more East African than Indonesian.



<h2 class="wp-block-heading" id="h-humans-with-tools-and-strategy">Humans with tools and strategy</h2>



Researchers counted more than 300 bones marked by stone blades or flakes. Some show percussion scars where marrow was pounded out.



“The Sunda Shelf played an important role in the dispersal and evolution of hominin populations,” wrote Berghuis and colleagues in their 2025 report. Others bear parallel slices typical of tendon removal.&nbsp;



“Thus far, hominin <a href="https://www.earth.com/news/archaeopteryx-fossil-soft-tissue-flight-evolution-proves-darwin-right/">fossils</a> from submerged Sundaland were not available.” The Madura Strait fragments break that drought. Underscoring the novelty of the find.&nbsp;



Tool cut geometry matches <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC4920301/" target="_blank" rel="noreferrer noopener">Acheulean‑derived technologies</a> already known from Java’s terrestrial sites. That continuity supports the idea that people followed rivers seasonally, carrying simple gear that was easy to replace when tools were lost in mud or water.



<h2 class="wp-block-heading" id="h-what-the-skulls-add-to-the-story">What the skulls add to the story</h2>



Although each piece is only a few inches across, the brow ridge profile and bone thickness match late <a href="https://pubmed.ncbi.nlm.nih.gov/18479734/" target="_blank" rel="noreferrer noopener">Homo erectus skulls</a> dug from Ngandong and Sambungmacan farther up the Solo. 



That link pushes the species’ confirmed range hundreds of miles east, showing it followed river corridors onto the shelf when sea level was low.



One fragment comes from an adolescent, the other from a lightly built adult. Their presence alongside butchered game hints that family groups, not lone hunters, roamed the valley.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/maduro-strait_indonesia_homo-erectus_skull_credit-ScienceDirect_1.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/maduro-strait_indonesia_homo-erectus_skull_credit-ScienceDirect_1s.webp" alt="3D surface images of MS1 and Sambungmacan 3 (anterior view). This comparative skull has the closest metric and morphological match with MS1. Credit: ScienceDirect" class="wp-image-1976534"/></a><figcaption class="wp-element-caption">3D surface images of Madura Strait (MS1) and Sambungmacan 3 (anterior view) fossils. This comparative skull has the closest metric and morphological match with MS1. Click image to enlarge. Credit: ScienceDirect</figcaption></figure>



Because no fire traces were found, the visitors probably camped on higher terraces that are now long submerged. 



The bones they left behind washed into lower channels during seasonal floods and were sealed beneath overbank sand.



<h2 class="wp-block-heading" id="h-looking-for-cousins-beneath-the-waves">Looking for cousins beneath the waves</h2>



The Solo River was only one of many channels draining Sundaland. As survey vessels map more buried valleys, archaeologists expect to meet a wider cast: <a href="https://www.earth.com/news/mysterious-denisovan-species-humans-lived-undisturbed-tibetan-plateau-160000-years/">Denisovans</a>, perhaps, or even the diminutive <a href="https://australian.museum/learn/science/human-evolution/homo-floresiensis/" target="_blank" rel="noreferrer noopener">Homo floresiensis</a>.



Every bucket of dredged sand now promises not just minerals for construction but clues to human origins. 



Underwater archaeology once focused on shipwrecks; now it is turning to paleolandscapes that could double the search area for early humans in Southeast Asia.



The Indonesian government is drafting guidelines that will require sand‑mining companies to report <a href="https://www.earth.com/news/scientists-find-a-47-million-year-old-cicada-fossil-with-preserved-wing-details/">fossil</a> finds within 48 hours. 



Those rules could transform commercial dredges into accidental research partners, expanding the data set at a fraction of normal field costs.



For now the Madura Strait cache stands alone, yet it already stretches the timeline of underwater archaeology in Asia. 



Skulls, riverbeds, and giant beast bones, all locked together in a drowned landscape, remind us that today’s ocean floor was yesterday’s hunting ground.



The study is published in <a href="https://www.sciencedirect.com/science/article/pii/S295023652500012X?via%3Dihub" target="_blank" rel="noreferrer noopener">Quaternary Environments and Humans</a>.



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Archaeologists find 140,000-year-old human and animal remains at the bottom of the ocean

Off the eastern tip of Java, dredging barges dragged up...

The sea spider, those spindly marine oddities that seem composed almost entirely of legs and claws, just given up their genetic secrets.



An international effort led by the <a href="https://www.univie.ac.at/en/">University of Vienna</a> and the <a href="https://www.wisc.edu/">University of Wisconsin–Madison</a> has delivered the first chromosome-level genome for Pycnogonum litorale, a species common in North Atlantic tide pools.



Stretching across 57 pseudo-chromosomes and paired with extensive developmental transcriptomes, the assembly offers an unprecedented look at how an arthropod can evolve such an extreme body plan. This includes a nearly vanishing abdomen and internal organs that spill far into its limbs.



<h2 class="wp-block-heading" id="h-mapping-the-sea-spider-genome">Mapping the sea spider genome</h2>



To achieve a genome this contiguous, the team combined long-read sequencing with Hi-C proximity data. Long reads captured tens of thousands of DNA bases at a stretch. This helped bridge the repetitive regions that routinely break short-read assemblies.



Hi-C, which measures how DNA folds inside the nucleus, then provided a “scaffolding” map that placed those long contigs into chromosomal order.



“The genomes of many non-canonical laboratory organisms are challenging to assemble, and Pycnogonum is no exception," said first author Nikolaos Papadopoulos, a zoologist at the University of Vienna. 



"Only the combination of modern high-throughput data sources made a high-quality genome possible. This can now serve as a stepping stone for further research.”



Because <a href="https://www.earth.com/news/surprising-breeding-behaviors-of-giant-sea-spiders-revealed/">sea spiders</a> are not standard lab animals, researchers collected specimens by hand, often prying them from kelp during low tide. They then rushed them back to the lab for nucleic acid extraction.



The payoff is a reference genome that joins spider, <a href="https://www.earth.com/news/fossil-reveals-the-first-ancestors-of-scorpions-and-spiders/">scorpion</a>, mite, and horseshoe crab assemblies on public databases. Yet it lacks the duplications that mark other arachnid genomes, making it a vital baseline for evolutionary comparisons.



<h2 class="wp-block-heading" id="h-vanished-gene-vanished-abdomen">Vanished gene, vanished abdomen</h2>



The analysis focused on Hox genes, key developmental regulators shared by animals from fruit flies to humans. One gene turned up missing: abdominal-A (abd-A).



In most arthropods, abd-A helps establish the rear-body segments that carry guts and reproductive organs. Sea spiders, with their virtually absent abdomens, appear to have dispensed with both the physical structure and its genetic architect.



“In arthropods, Hox genes play a central role in the correct specification of the different body segments, explained co-author Andreas Wanninger, who co-led the Vienna team. "In many other animal groups they are essential ‘master controllers’ during body plan development.” 



The disappearance of abd-A mirrors patterns seen in <a href="https://www.earth.com/news/how-mites-survived-without-sex-for-millions-of-years/">mites</a> and barnacles, two other arthropod groups that have independently shrunk or lost their hind segments.



<h2 class="wp-block-heading" id="h-sea-spiders-skipped-genome-doubling">Sea spiders skipped genome doubling</h2>



Spiders and scorpions carry extra copies of almost every gene, relics of an ancient whole-genome duplication that likely fueled innovations such as silk glands and complex venom cocktails.



P. litorale shows no sign of that event. Because sea spiders sit at the very base of the chelicerate lineage, the simplest explanation is that the duplication occurred later. It likely arose within the spider-scorpion branch, rather than in the common ancestor of all chelicerates.



That finding reshapes timelines for when gene families expanded and may help researchers pinpoint which duplications underlie spider-specific traits.



<h2 class="wp-block-heading" id="h-tools-for-growth-and-repair">Tools for growth and repair</h2>



Beyond raw sequence, the consortium generated RNA profiles from embryos and juveniles, capturing when each gene flicks on and off as new body segments form.



Those developmental datasets make the sea spider a promising model for studies of ancestral arthropod development, limb regeneration, and physiological resilience in cold, nutrient-poor seas.



Georg Brenneis, an expert in arthropod development at the University of Vienna, is a senior author of the study.



“From an evolutionary developmental perspective, sea spiders are very interesting: their mode of development may be ancestral for arthropods, but at the same time they boast multiple body plan innovations unique to themselves. Beyond this, they also possess remarkable regenerative abilities.” 



“Now that we have the genome and comprehensive datasets on gene activities during development, we can systematically study all of these aspects on the molecular level,” he said.



<h2 class="wp-block-heading" id="h-editing-limbs-and-trunk">Editing limbs and trunk</h2>



With <a href="https://www.earth.com/news/crispr-used-to-remove-extra-chromosomes-in-down-syndrome-and-restore-cell-function/">CRISPR</a> editing becoming feasible in marine invertebrates, investigators can now ask how the remaining sea spider Hox genes choreograph eight elongated walking legs and a tubular trunk. They can also explore how the animals quickly regrow lost appendages.



Comparative physiologists might search the genome for stress-response genes that let sea spiders thrive in icy fjords, while ecological genomics teams could examine how gene flow operates across their wide geographic ranges.



<h2 class="wp-block-heading" id="h-tracing-ancient-sea-spider-cousins">Tracing ancient sea spider cousins</h2>



Without the duplication, shared sea spider genes likely existed as single copies in the last common chelicerate ancestor.



Aligning those sequences will clarify where new venom toxins arose, when silk machinery evolved, and how immune genes diversified.



The genome also lets scientists investigate regulatory DNA - enhancers, promoters, and non-coding RNAs. These elements rewired a conventional arthropod blueprint into the minimalist sea spider form.



<h2 class="wp-block-heading" id="h-expanding-the-genomic-catalog">Expanding the genomic catalog</h2>



The authors envision expanding the catalog to additional sea spider species to test whether abd-A loss is universal. They also aim to map gains and losses of other developmental genes across the group’s 1,300 known species.



Such work could uncover genetic shortcuts to extreme morphological change - insights that extend far beyond any single marine arthropod.



For now, the P. litorale genome stands as a milestone: the first high-quality reference for the world’s most enigmatic chelicerates. It’s also a reminder that even life’s strangest branches follow molecular rules that genomics can finally reveal.



The study is published in the journal <a href="https://bmcbiol.biomedcentral.com/articles/10.1186/s12915-025-02276-x">BMC Biology</a>.



Image Credit: Richard Lord/ <a href="https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode.en">CC BY-NC-SA 4.0</a>



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All legs, no guts: Sea spider genome stuns scientists

The sea spider, those spindly marine oddities that seem composed...

High in northern Peru, three frogs no bigger than a thumbprint have stepped out of anonymity and into the scientific spotlight. Their world is a maze of wet cliffs, dripping bromeliads, and wind‑scoured ridges where moss carpets the rocks.



“They’re <a href="https://www.earth.com/news/world-frog-day-2025-protecting-natures-tiny-guardians/">small</a> and unassuming, but these frogs are powerful reminders of how much we still don’t know about the Andes,” said Germán Chávez of the Center for Ornithology and Biodiversity (<a href="https://corbidi.org/">CORBIDI</a>). 



Chávez and his colleagues trekked those ridges between 2021 and 2024, often in freezing rain, to reach calling sites above 9,000 feet.&nbsp;



<h2 class="wp-block-heading" id="h-mountains-support-unique-frog-species">Mountains support unique frog species</h2>



The <a href="https://blog.pensoft.net/2025/06/27/hidden-gems-in-the-mist-three-new-frog-species-uncovered-in-northern-peru/cordillera-de-huancabamba-1/" target="_blank" rel="noreferrer noopener">Cordillera de Huancabamba</a> forms a natural break in the Andes, splitting watersheds and isolating species. 



Ecologists classify the region as a <a href="https://www.cepf.net/sites/default/files/tropicalandes_techsummary.pdf" target="_blank" rel="noreferrer noopener">biodiversity hotspot</a>, one of only thirty‑five on Earth where extraordinary endemism collides with severe habitat loss.



"The Cordillera de Huancabamba is not just a remote range - it's a living archive of biodiversity and cultural legacy," said Wilmar Aznaran. "And we've barely scratched the surface."



Isolation breeds novelty, and novelty fills the genus Pristimantis. With 619 described species, Pristimantis is now the most diverse <a href="https://www.earth.com/news/whistling-forest-frogs-recently-discovered-may-be-wiped-out-before-we-learn-about-them/">amphibian</a> genus on the planet.



The new frogs, Pristimantis chinguelas, P. nunezcortezi, and P. yonke, occupy different niches along the same ridge. One clings to cliff faces, one prowls leaf litter beside clear streams, and the smallest tucks itself deep inside tank bromeliads.



<h2 class="wp-block-heading" id="h-confirming-the-new-species">Confirming the new species</h2>



Night surveys began after dusk, when temperatures hovered near 50 °F and fog erased headlamp beams. Team members listened for faint “peep” notes that barely rose above dripping leaves. 



Finding a caller did not end the chase. Each frog had to be photographed, swabbed for DNA, measured, and released without harming delicate skin.



Back in Lima, the researchers compared mitochondrial 16S sequences. Genetic distances exceeded the three‑percent threshold herpetologists often use to flag separate <a href="https://www.earth.com/news/missing-frog-species-alsodes-vittatus-resurfaces-after-130-years/">species</a>, clinching the case for formal description.



<h2 class="wp-block-heading" id="h-many-amphibians-are-poorly-studied">Many amphibians are poorly studied </h2>



All three newcomers enter the IUCN books as <a href="https://www.thebhs.org/publications/the-herpetological-bulletin/issue-number-169-autumn-2024/4079-03-how-many-data-deficient-amphibians-are-threatened-iucn-red-list-assessments-for-amphibian-species-previously-classed-as-data-deficient" target="_blank" rel="noreferrer noopener">Data Deficient</a>, meaning scientists lack enough information to judge extinction risk. 



The label sounds neutral, yet recent reassessments show that roughly half of amphibians that start as Data Deficient later prove threatened.



Formal names unlock funding and legal tools that nameless creatures rarely receive. Conservation plans, environmental‑impact statements, and protected‑area budgets almost always hinge on a taxon’s standing in recognized databases.



<h2 class="wp-block-heading" id="h-indicators-of-climate-shifts">Indicators of climate shifts</h2>



The Cordillera de Huancabamba isn't just a biological goldmine, it’s wrapped in layers of folklore. In nearby villages, frogs are often seen as signs of rain or omens tied to agriculture and spiritual beliefs.



This cultural lens makes local communities key allies for conservation. When researchers name <a href="https://www.earth.com/news/frogs-lead-the-way-in-developing-new-antibiotics/">species</a> after regional icons or traditions, like P. yonke, they honor local identity and encourage stewardship.



Unlike most frogs, species in the <a href="https://www.inaturalist.org/taxa/64811-Pristimantis" target="_blank" rel="noreferrer noopener">Pristimantis genus</a> bypass the tadpole stage entirely. They hatch from eggs as fully formed froglets, ready to climb, hop, and call without ever entering water.



This reproductive shortcut allows them to thrive in places where standing water is rare or seasonal. It also makes them sensitive indicators of climate shifts and microhabitat changes in mountain ecosystems.



<h2 class="wp-block-heading" id="h-frog-species-in-fire-prone-habitats">Frog species in fire-prone habitats</h2>



Each frog occupies an area smaller than four square miles, hemmed in by crop fields and fire scars. Peru recorded about 10,400 wildfires in 2024, more than double its previous record, burning grasslands and cloud‑forest edges alike.



P. chinguelas calls from a road‑cut cliff where charred bamboo still smells of smoke. P. nunezcortezi shares a single stream corridor that now borders new potato plots.



P. yonke lives higher, inside bromeliads at roughly 9,800 feet, in what locals call the <a href="https://lacgeo.com/northern-andean-paramo" target="_blank" rel="noreferrer noopener">páramo</a>, a chilly grassland‑wetland mosaic perched above the treeline. 



Páramo vegetation stores water like a sponge, so every lost bromeliad weakens both the frogs and the human communities farther down‑slope.



“Exploring this area is more than fieldwork - it’s an immersion into wilderness, culture, and resilience,” said Karen Victoriano‑Cigüeñas.&nbsp;



"Many of these mountain&nbsp;ridges&nbsp;are isolated, with no roads and extreme terrain," noted Ivan Wong. "The weather shifts within minutes, and the steep cliffs make every step a challenge. It's no wonder so few scientists have worked here before. But that's exactly why there's still so much to find."



<h2 class="wp-block-heading" id="h-protecting-the-new-frog-species">Protecting the new frog species </h2>



No one has recorded the breeding calls of P. nunezcortezi or P. yonke, so females remain unverified. Diet, predators, and lifespan also remain mysteries for all three species.



Future expeditions will test whether the frogs persist on neighboring ridges or whether each ridge hosts its own micro‑endemic. 



Acoustic monitors and <a href="https://royalsocietypublishing.org/doi/10.1098/rspb.2019.2353" target="_blank" rel="noreferrer noopener">eDNA traps</a> could reveal silent populations hiding in moss tunnels or bromeliad tanks beyond the reach of hikers.



For now, the frogs depend on local goodwill. Community fire patrols, low‑impact grazing, and small protected micro‑reserves can buy time while researchers gather the missing data.



The study is published in the journal <a href="https://evolsyst.pensoft.net/article/148522/" target="_blank" rel="noreferrer noopener">Evolutionary Systematics</a>.



Image Credit: Germán Chávez et. al



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Three new frog species found in Peru face an uncertain future

High in northern Peru, three frogs no bigger than a...

The,Galapagos,Islands.,Ecuador.,Galapagos,Tortoise,In,Motion.,Island,Of

For centuries, turtles have fascinated people with their remarkably long lifespans.&nbsp;A new study reveals something even more extraordinary. Cancer is extremely rare in turtles, which makes them a promising model for cancer research.



The study, led by Dr. Ylenia Chiari at the <a href="https://www.nottingham.ac.uk/">University of Nottingham</a>, shows that cancer affects only about 1% of turtles. This rate is much lower than in mammals or birds.



The team analyzed decades of health records from zoos across Europe and the United States, including <a href="https://www.chesterzoo.org/">Chester Zoo</a>. 



The findings suggest that <a href="https://www.earth.com/news/world-turtle-day-2025-ancient-creatures-with-modern-challenges/">turtles</a> could help scientists learn new ways to prevent or fight cancer in humans.



<h2 class="wp-block-heading" id="h-turtles-rarely-get-cancer">Turtles rarely get cancer</h2>



The experts reviewed necropsy records from hundreds of zoo turtles. According to the detailed analysis, only about 0.34% of the turtles examined showed any abnormal growth. 



Cancer cases were even rarer. Most cancers found were isolated cases, and they rarely spread. Turtles show no clear pattern of cancers affecting specific organs.



Compared to <a href="https://www.earth.com/news/beating-the-heat-how-sea-turtles-cope-with-warming-waters/">mammals</a> and birds, turtles remain outliers. Mammals have average cancer rates of 10 percent, while birds have rates around three percent. By contrast, cancer rates in turtles are consistently under one percent.



<h2 class="wp-block-heading" id="h-turtles-have-strong-cancer-defense">Turtles have strong cancer defense</h2>



Turtles have slow metabolisms and strong defenses against oxidative stress. These traits reduce cellular damage over time.



Genomic studies revealed that turtles, especially Galapagos and Aldabra giant tortoises, have unique genetic mutations. These mutations enhance tumour suppression and help maintain DNA stability.



Functional tests on Galapagos giant tortoise cells showed an ability to trigger cell death early. This prevents damaged cells from becoming cancerous. <a href="https://www.earth.com/news/turtle-heads-reveal-an-ancient-reptilian-secret/">Turtles</a> also exhibit robust antioxidant responses, even under stress.



Turtles’ low metabolic rates also limit the buildup of harmful byproducts. This may explain their strong cancer resistance.



<h2 class="wp-block-heading" id="h-turtles-stay-cancer-free-despite-size">Turtles stay cancer-free despite size</h2>



Turtles challenge common biological patterns. Large, long-lived species often have higher cancer risks because of more cells. But turtles defy this rule.



Some species, like Galapagos and Aldabra tortoises, weigh over 660 pounds. Others, such as leatherback sea turtles, can exceed 1,100 pounds. Still, their cancer rates remain extremely low.



“Turtles, especially iconic species like Galapagos and Aldabra giant <a href="https://www.earth.com/news/young-sea-turtles-swim-and-choose-their-paths-instead-of-drifting/">tortoises</a>, are famous for living long lives and growing to tremendous sizes," noted Dr. Chiari.



"You’d expect that to mean more cancer, but our study, which combines decades of zoo records with previous research, shows how incredibly rare cancer is in these animals." 



Dr. Chiari said that the study highlights turtles as an untapped model for understanding cancer resistance and healthy aging, and it shows the vital role zoos play in advancing science through collaboration.



<h2 class="wp-block-heading" id="h-turtle-secrets-and-medical-insights">Turtle secrets and medical insights</h2>



According to study lead author Dr. Scott Glaberman from the University of Birmingham, biodiversity has a lot to teach us about how the world works. 



"While fascinating in their own right, extreme species like giant tortoises may have already solved many of the problems humans face, including those related to aging and cancer. That makes biodiversity doubly worthy of protection,” said Dr. Glaberman.



Dr Helena Turner, Research Officer at Chester Zoo, said her team has been long been committed to detailed health monitoring and the long-term care of their animals. 



"It’s fantastic to see these efforts not only contribute to advancing scientific knowledge around cancer resistance but also support vital conservation work to protect these remarkable species that may hold keys to medical breakthroughs benefiting both wildlife and humans,” said Dr. Turner.



<h2 class="wp-block-heading" id="h-studying-turtles-in-the-wild">Studying turtles in the wild</h2>



Much of the current data comes from zoo populations. Zoo turtles often live longer than wild ones. This could increase chances of detecting cancer. However, researchers still lack cancer data from wild turtles.



Tracking turtles across their long lifespans remains difficult. Many species live as long as humans. Without decades of monitoring, it is hard to collect enough data.



Researchers suggest using turtle cell lines for laboratory studies. These experiments could reveal how turtle cells respond to stress, DNA damage, and other cancer-related triggers.



Such studies may unlock hidden mechanisms behind turtles’ resistance to cancer and aging. Insights from turtles could help both human medicine and wildlife conservation.



<h2 class="wp-block-heading" id="h-conservation-efforts-remain-critical">Conservation efforts remain critical</h2>



Many turtle species face extinction threats. The <a href="https://www.iucnredlist.org" target="_blank" rel="noreferrer noopener">IUCN Red List</a> categorizes several as Endangered or Critically Endangered.



Threats include habitat loss, illegal wildlife trade, and climate change. Many zoos in the study also lead breeding programmes to save these species.



Protecting turtles could also protect vital genetic secrets that benefit human health. Their remarkable resistance to cancer makes their conservation even more urgent.



The study is published in the journal <a href="https://academic.oup.com/bioscience/advance-article/doi/10.1093/biosci/biaf100/8185759" target="_blank" rel="noreferrer noopener">BioScience</a>.



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Turtles may hold the secret to cancer prevention in humans

For centuries, turtles have fascinated people with their remarkably long...

In the arid, fossil-rich landscape of Arizona’s Petrified Forest National Park, a team of paleontologists stumbled across something unexpected. The experts found the fossilized jawbone of a pterosaur that may be the oldest ever found in North America.



The discovery came from a remote site that revealed not just one remarkable creature, but a whole ecosystem preserved in stone.



The study was led by scientists from the Smithsonian’s <a href="https://www.si.edu/museums/natural-history-museum">National Museum of Natural History</a> and <a href="https://www.nps.gov/pefo/index.htm" target="_blank" rel="noreferrer noopener">Petrified Forest National Park</a>. The research introduces a new pterosaur species alongside more than 1,000 other fossils.



Some of these include one of the world’s oldest turtle specimens. Together, the fossils paint a vivid picture of life just before one of Earth’s biggest mass extinctions.



<h2 class="wp-block-heading" id="h-life-before-mass-extinction">Life before mass extinction</h2>



The pterosaur fossils come from rock layers that date back to the Late <a href="https://www.earth.com/news/climate-did-not-impact-dinosaur-abundance-in-the-triassic/">Triassic</a> period. During this time, ancient amphibians and crocodile-like reptiles lived side by side with animals that would go on to shape the future of the planet, including early turtles, frogs, and flying reptiles.



“The site captures the transition to more modern terrestrial vertebrate communities, where we start seeing groups that thrive later in the <a href="https://www.earth.com/news/dinosaurs-were-not-the-only-animals-that-grew-fast-during-the-mesozoic/">Mesozoic</a> living alongside these older animals that don’t make it past the Triassic,” said study lead author Ben Kligman.



This glimpse into prehistoric life is especially valuable because it dates to just before the end-Triassic extinction - about 201.5 million years ago - when massive volcanic eruptions dramatically altered Earth’s climate. 



The event wiped out roughly 75% of all species, paving the way for dinosaurs to rise to dominance.



<h2 class="wp-block-heading" id="h-fossils-hidden-by-ash">Fossils hidden by ash</h2>



Direct fossil evidence from just before this extinction is hard to come by. Few fossil-rich outcrops from this time exist, but Petrified Forest National Park is one of the rare exceptions. 



Known for its colorful layers of petrified wood and Triassic fossils, the park has long been a treasure trove for paleontologists.



One rock layer, called the Owl Rock Member, has proven especially important. It’s full of <a href="https://www.earth.com/news/fire-and-ice-volcanic-ash-plays-a-surprising-role-in-cloud-formation/">volcanic ash</a>, which helped scientists date it precisely to around 209 million years ago. These are some of the park’s youngest rocks - but also among its least explored.



Study co-author William Parker explained that the Owl Rock exposures are tucked away in extremely remote areas. Few teams have been able to study them in detail.



In 2011, a research group led by Kay Behrensmeyer decided to take on the challenge. Braving the rugged terrain - complete with rattlesnakes and wild horses - they went in search of mammal-like fossils. 



What they found instead was a densely packed bonebed, full of life from a vanished world.



“That’s the fun thing about paleontology: you go looking for one thing, and then you find something else that’s incredible that you weren’t expecting,” said Kligman, who started working at the site during his PhD studies in 2018.



<h2 class="wp-block-heading" id="h-ancient-life-buried-by-floods">Ancient life buried by floods</h2>



Back in the Triassic, this part of Arizona was located near the equator and sat in the center of the supercontinent <a href="https://www.earth.com/earthpedia-articles/supercontinents-101-pannotia-gondwana-and-pangea/">Pangaea</a>. 



The land was semi-arid, with winding river channels and a seasonal flood cycle. One of those floods likely buried the animals that are now preserved in the bonebed.



The fossil layer was so dense with tiny remains that collecting them onsite was impossible. Instead, researchers carved out large blocks of sediment, wrapped them in plaster, and brought them back to the lab.



Many of these blocks were sent to the Smithsonian’s FossiLab, where volunteers spent thousands of hours carefully exposing the bones. 



<h2 class="wp-block-heading" id="h-small-fossils-major-clues">Small fossils, major clues</h2>



The rivers teemed with fish like coelacanths and freshwater sharks. Giant amphibians - some stretching over six feet long - swam through the streams. On land, armored herbivores and <a href="https://www.earth.com/news/ancient-crocodile-like-beast-was-a-terrifying-predator/">crocodile-like predators</a> ruled.



At the same time, smaller creatures were starting to make their mark. The team identified early frogs, relatives of today’s tuataras, and a turtle with spike-like armor that could fit in a shoebox. 



The remains of a small pterosaur were also hidden among the layers - just one part of a fossil record that shows how quickly new groups were emerging and spreading across Pangaea.



“This suggests that turtles rapidly dispersed across Pangaea, which is surprising for an animal that is not very large and is likely walking at a slow pace,” said Kligman.



<h2 class="wp-block-heading" id="h-pterosaur-that-perched-like-a-bird">Pterosaur that perched like a bird</h2>



One of the most exciting finds was a jawbone with teeth still in place. It belonged to a small pterosaur, one of the first vertebrates capable of powered flight. This early flier could have perched on a person’s shoulder.



The pterosaur fossil was uncovered by Suzanne McIntire, a volunteer who spent 18 years working in the FossiLab.



“What was exciting about uncovering this specimen was that the teeth were still in the bone, so I knew the animal would be much easier to identify,” McIntire said.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/pterosaur_Eotephradactylus-mcintireae_Arizona_illustration_credit-Brian-Engh_1big.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/pterosaur_Eotephradactylus-mcintireae_Arizona_illustration_credit-Brian-Engh_1s.webp" alt="An artist's reconstruction of the fossilized landscape, plants and animals found preserved in a remote bonebed in Petrified Forest National Park in Arizona. The newly described pterosaur Eotephradactylus mcintireae is seen eating an ancient ray-finned fish alongside an early species of turtle and an early frog species, with the skeleton of an armored crocodile relative lying on the ground and a palm-like plant growing in the background. Credit: Brian Engh" class="wp-image-1977432"/></a><figcaption class="wp-element-caption">An artist's reconstruction of the fossilized landscape, plants and animals found preserved in a remote bonebed in Petrified Forest National Park in Arizona. The newly described pterosaur Eotephradactylus mcintireae is seen eating an ancient ray-finned fish alongside an early species of turtle and an early frog species, with the skeleton of an armored crocodile relative lying on the ground and a palm-like plant growing in the background. Click image to enlarge. Credit: Brian Engh</figcaption></figure>



The wear on the teeth gave scientists a clue about the pterosaur’s diet. It likely fed on armored fish that were common in the area. 



The new species was named Eotephradactylus mcintireae, which translates to “ash-winged dawn goddess." This title honors McIntire, who retired last year.



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



Pterosaurs were flying reptiles that existed during the time of <a href="https://www.earth.com/news/where-did-dinosaurs-come-from-missing-fossils-hold-the-secret/">dinosaurs</a>. They were the first animals with backbones to evolve powered flight, well before birds or bats came on the scene.



Powered by skin stretched across an extended fourth finger, they ranged in size and shape from something no larger than a crow to giants with wings up to 30 feet or more.



Pterosaurs were not dinosaurs. They formed their own group of reptiles and possessed special adaptations for flight. Some flew above coastlines, while others preyed on fish or small land animals inland.



The new fossil contributes to what is known about those early birds and how they expanded around the globe.



The full study was published in the journal <a href="https://www.pnas.org/doi/10.1073/pnas.2505513122" target="_blank" rel="noreferrer noopener">Proceedings of the National Academy of Sciences</a>.



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North America's oldest known pterosaur discovered in a petrified forest

In the arid, fossil-rich landscape of Arizona’s Petrified Forest National...

Most people think aging always brings health problems. Inflammation seems like a part of getting older. It slowly builds up, leading to serious diseases. 



Doctors call this slow-burning process “inflammaging.” But not everyone is sure that this process is unavoidable. Some scientists are starting to ask new questions. Does every species experience inflammaging? Is it something we can avoid?



Elaine Guevara from <a href="https://duke.edu" target="_blank" rel="noreferrer noopener">Duke University</a> studies primates, a group that includes both lemurs and humans. Her work focuses on aging and how it works in different species.



Recently, Guevara began looking at lemurs for answers. These animals may look far removed from humans, but their biology has much to teach us. In fact, her latest <a href="https://www.earth.com/news/endangered-lemurs-millions-of-years-of-diversity-at-risk/">research</a> suggests that inflammation during aging may not be as inevitable as people believe.



<h2 class="wp-block-heading" id="h-lemurs-challenge-our-view-of-aging">Lemurs challenge our view of aging </h2>



Guevara's study was focused on two <a href="https://www.earth.com/news/hormones-influence-power-and-peace-in-lemur-society/">species</a>: the ring-tailed lemur and the sifaka lemur. These species have many similarities but also some key differences. They have different lifespans and distinct life patterns, which makes them perfect for comparison.



Lemurs share an ancient ancestor with humans. This connection makes them valuable for studying human biology. Scientists often use primates to answer tricky questions about human health.



Guevara wanted to see if lemurs show signs of inflammaging as they grow older. The idea was simple. If inflammation rises in both humans and lemurs, it might be a natural part of aging for all primates. But the results took everyone by surprise.



<h2 class="wp-block-heading" id="h-lemurs-aged-without-more-inflammation">Lemurs aged without more inflammation</h2>



The team expected to see clear signs of inflammaging in lemurs. This would have matched patterns seen in humans. But that is not what happened.



“Contrary to our predictions, neither <a href="https://www.earth.com/news/hibernation-allows-lemurs-to-slow-down-their-aging/">species</a> showed age-related change in either marker of oxidative stress," said Guevara.



"Neither lemur species exhibited age-related change in inflammation; if anything, contrary to our prediction, ring-tailed lemurs showed marginal declines in inflammation with age."



The findings challenge what many people think about aging. If lemurs do not show inflammaging, maybe it is not something all species must face.



<h2 class="wp-block-heading" id="h-is-inflammaging-really-unavoidable">Is inflammaging really unavoidable?</h2>



Lemurs are not alone in this unexpected pattern. Researchers have seen similar results in other primate species. Christine Drea, a scientist involved in the lemur study, explained the bigger picture.



According to Drea, the research suggests inflammaging is not universal across primates. If that is true, it raises an important question. Could some humans also avoid inflammaging?



The idea turns traditional thinking about aging upside down. Many believed inflammaging was simply part of life, but the study shows it might not be that simple.



Scientists are now looking at aging in a whole new way. They are asking if the right conditions might prevent or delay inflammation in humans too.



<h2 class="wp-block-heading" id="h-inflammaging-causes-health-issues">Inflammaging causes health issues</h2>



Inflammaging sounds like a problem only scientists worry about, but it affects millions of people. As people age, their bodies often enter a state of low-level inflammation. This quiet <a href="https://www.earth.com/news/endangered-lemurs-now-prey-for-equally-endangered-fosas/">process</a> can cause serious harm over time.



Inflammaging connects to many common diseases. These include heart problems, strokes, diabetes, cancer, and arthritis.



Doctors and researchers are working hard to find solutions. If they can understand why inflammaging happens, they may find ways to stop it.



The lemur study offers new hope. It suggests that inflammaging is not locked into our biology. That alone is an exciting discovery.



<h2 class="wp-block-heading" id="h-the-challenge-of-studying-lemurs">The challenge of studying lemurs</h2>



Studying aging in lemurs is not easy. The animals cannot explain their health. Researchers had to come up with a safe way to collect data.



"Our role at the beginning was planning, designing, brainstorming, comparing and getting these samples,” said Drea.



The team collected urine samples from the lemurs. This method allowed them to study oxidative stress and inflammation without harming the animals.



The research was conducted at the Duke Lemur Center. This facility only allows non-invasive studies. The lemurs remained unharmed throughout the entire project.



<h2 class="wp-block-heading" id="h-future-research-on-lemurs-and-aging">Future research on lemurs and aging</h2>



Guevara now wants to expand her research. Her next focus will be wild lemurs living in their natural environment.



“There are a lot of good reasons to think that aging can be quite different in captivity and in the wild, and that in itself, is informative to evaluating the degree to which human inflammation is intrinsic versus environmental,” she said.



Wild lemurs face many challenges that captive lemurs do not. Their diet, stress, and activity levels all vary. 



By studying lemurs, scientists can learn whether environment shapes aging. The ongoing research could reveal even more about human aging.



<h2 class="wp-block-heading" id="h-lemurs-offer-new-aging-insights">Lemurs offer new aging insights</h2>



People around the world are living longer. However, many of those extra years come with health issues. Inflammaging is a major reason for this.



Guevara believes her work is an important first step toward finding new solutions. "These insights are essential for mitigating disability and improving quality of life in later years."



This study shows that aging does not look the same in every species. Lemurs have shown a very different path. They age without the same inflammation humans often face. 



Researchers now have a fresh question to explore. Can humans also avoid inflammaging? The answer could change how we think about growing older. It could shift how we approach health care for aging populations.



Lemurs may not have provided all the answers yet, but they have certainly started an important conversation.



The study is published in the <a href="https://link.springer.com/article/10.1007/s00360-025-01619-y" target="_blank" rel="noreferrer noopener">Journal of Comparative Physiology B</a>. 



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Lemurs reveal surprising new clues about healthy aging

Most people think aging always brings health problems. Inflammation seems...

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