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 review pulls together decades of research on tire wear particles (TWPs) - the tiny bits that break off tires and get washed away. It turns out wind and rain can sweep huge amounts of these fragments off highways and straight into nearby streams and ponds.



In heavy-traffic zones, TWPs can make up 50 to 90 percent of all <a href="https://www.earth.com/news/car-tires-are-a-big-source-of-microplastics-pollution-but-what-about-mountain-bikes/">microplastics</a> that run off roads during rainfall. When soils are included, nearly 45 percent of microplastics found on land or in freshwater environments can be traced to tire abrasion.



Concentrations recorded in field samples vary wildly - from just 0.00001 mg per liter to an astonishing 10,000 mg per liter. These extremes highlight the presence of localized hotspots.



<h2 class="wp-block-heading" id="h-tires-release-a-toxic-mix">Tires release a toxic mix</h2>



When it comes to tires, speed and grip matter more than ecological impact. The review lists 2,456 different chemicals in tire rubber - and lab tests show that at least 144 of them can leach out.



Prominent among them are hexamethoxymethyl-melamine, dibutyl phthalate, and the antioxidant 6-PPD, which transforms into its highly toxic quinone derivative. 



Manufacturers embed <a href="https://www.earth.com/news/heavy-metal-pollution-threatens-marine-life-and-human-health/">heavy metals</a> - like zinc, manganese, cadmium, and lead - into the polymer matrix as vulcanizing agents and fillers.



Hans-Peter Grossart of the <a href="https://www.igb-berlin.de/en">Leibniz Institute of Freshwater Ecology and Inland Fisheries</a> is a co-author of the study.



“During the leaching process, tire abrasion releases more chemicals than thermoplastics such as PE. We also assume that more substances are leached out than we already know,” he said.



<h2 class="wp-block-heading" id="h-tire-dust-disrupts-ecosystems">Tire dust disrupts ecosystems</h2>



Laboratory exposure studies reveal that tire particles and their leachates prompt oxidative stress, DNA damage, immune suppression, and developmental defects in a wide array of aquatic organisms. Affected species show reduced feeding, stunted growth, and lower reproductive success.



Scaling up, the review links these individual ailments to shifts in community composition, which in turn disrupt nutrient cycles and diminish biodiversity. 



Changes in microbial and algal communities could also disrupt how carbon and nitrogen cycle through the environment - processes that are key to <a href="https://www.earth.com/news/it-took-200-million-years-for-earth-to-get-its-oxygen/">oxygen</a> production and clean water.



<h2 class="wp-block-heading" id="h-warming-worsens-toxic-effects">Warming worsens toxic effects</h2>



Rising temperatures and freshwater acidification are likely to make the ecological impact of tire particles even worse.



Higher temperatures accelerate chemical reactions, increasing the rate at which additives leach from particles, while lower pH can heighten metal solubility and bioavailability.



Grossart cautioned that these environmental shifts will likely exacerbate the effects of tire wear and its leaching by altering its toxicity and its interactive effects on microbial activity, <a href="https://www.earth.com/news/climate-change-is-draining-nutrients-from-the-oceans-surface/">nutrient</a> cycling, and the resilience of ecosystems.



<h2 class="wp-block-heading" id="h-tire-dust-sinks-near-roads">Tire dust sinks near roads</h2>



Studies indicate that wind can spread tire wear particles over a wide area. However, most fragments fall near their release points and accumulate along road verges, drainage ditches, and sediment beds.



The researchers estimate that only about two percent of tire particles carried by rivers reach the sea. That means capturing them earlier - at the watershed level - could have a big impact.



The review calls for physical barriers and improved drainage systems to trap particles before they reach natural waterways.



<h2 class="wp-block-heading" id="h-drivers-play-a-role-too">Drivers play a role too</h2>



The researchers suggest that tire manufacturers should explore alternative formulations with fewer hazardous additives.



They also urge urban planners to improve the separation between road surfaces and water bodies. Yet drivers also hold part of the solution.



“Effective reduction strategies involve the development of alternative tire manufacturers, and a better demarcation of roads and wastewater from natural areas," Grossart said. "Ultimately, everyone can make their own contribution with a prudent driving style.” 



<h2 class="wp-block-heading" id="h-calls-for-tire-pollution-limits">Calls for tire pollution limits</h2>



Despite the mounting evidence, major knowledge gaps persist. Standardized field protocols are rare, hindering cross-study comparisons, and most of the thousands of tire-derived chemicals remain untested for toxicity.



The review urges cross-disciplinary collaborations to develop real-world monitoring networks and predictive models. These tools would help regulators set science-based limits for TWP emissions.



The review highlights TWPs as a major but overlooked source of freshwater pollution, based on volume and chemical complexity.



Without concerted action - from product redesign to traffic management - the dust generated by every mile driven will continue to seep into <a href="https://www.earth.com/news/major-plastic-pollution-lurks-beneath-the-surface-of-rivers/">rivers</a> and lakes, carrying with it a suite of toxins that ecosystems must somehow absorb.



The review is published in the <a href="https://www.sciencedirect.com/science/article/abs/pii/S0301479725020353?via%3Dihub">Journal of Environmental Management</a>. 



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Tire particles flood freshwater with toxic microplastics

A new review pulls together decades of research on tire...

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...

We hear about minerals all the time. Lithium, cobalt, nickel, graphite, and rare earth elements appear in the news almost every week.



These minerals power phones, <a href="https://www.earth.com/news/dirty-power-the-hidden-climate-cost-of-electric-vehicles/">electric cars</a>, and military equipment. Countries want them, companies want them, and the competition for the minerals keeps growing.



While leaders plan and companies race, some scientists study a different part of the story. They ask questions about where these minerals come from and how they move underground.



Geologist Zachary Burton works on these questions. He studies natural processes instead of using drills or machines.



<h2 class="wp-block-heading" id="h-rare-earth-elements-are-hard-to-find">Rare earth elements are hard to find</h2>



"Rare earth elements aren't technically rare - they are somewhat ubiquitous at very low concentrations - but highly concentrated, economically attractive deposits are indeed rare and hard to find," Burton explained.



In the Department of Earth Sciences at <a href="https://www.montana.edu/">Montana State University</a>, Burton has been studying these elements for almost 15 years.



The problem is simple. Scientists do not fully understand how these minerals move or gather in one place.



"That's in large part because we don't even know many fundamental scientific processes of why they concentrate in certain areas and how they're moving around," Burton said.



<h2 class="wp-block-heading" id="h-a-desert-deep-in-antarctica">A desert deep in Antarctica</h2>



Burton recently studied these minerals in a very cold place: <a href="https://www.earth.com/news/antarctica-is-experiencing-rapid-plant-growth-concerning-scientists/">Antarctica</a>'s McMurdo Dry Valleys. This part of Antarctica is dry, windy, and extremely cold. It has unusual landscapes that look similar to other planets.



Burton’s team investigated how rare earth minerals move in this polar desert. They focused on salt ponds in the area, including Don Juan Pond, VXE-6 Pond, and Brine Pond Number 1.



The team found something intriguing. In Don Juan Pond, mineral levels were low in the center - likely because chemicals had washed them away.



However, minerals had gathered underground in two specific spots: one about 10 to 12 centimeters deep (roughly 4 to 5 inches) west of Don Juan Pond, and another about 4 to 7 centimeters deep (around 1.5 to 2.75 inches) beneath VXE-6 Pond.



<h2 class="wp-block-heading" id="h-freezing-and-melting-moves-minerals">Freezing and melting moves minerals</h2>



The places with more minerals had another feature. The soil there contained clay-like <a href="https://www.earth.com/news/rare-meteorites-provide-a-window-into-the-early-solar-system/">materials</a>. These formed through chemical changes.



The reason for this process was clear. Water froze and melted many times. The ponds also changed in size. These actions moved the minerals.



Water carried the minerals. When the water froze, the minerals stayed behind in the soil. This cycle repeated many times. Over the years, minerals gathered just below the surface.



Burton explained that similar things can happen in other cold areas. He pointed to Greenland and Ukraine, two places that are often in the news for their mineral resources.



"Rare earths are an area that's been relatively neglected these past decades in terms of scientific research, but now - with these critical minerals constantly making headlines - there's a whole lot to be learned in terms of where deposits are," he said.



<h2 class="wp-block-heading" id="h-from-antarctica-to-other-planets">From Antarctica to other planets</h2>



Burton’s research is not only about Earth. It also connects to space. The Dry Valleys in Antarctica are similar to places on <a href="https://www.earth.com/news/new-plan-terraform-mars-nanoparticles-would-make-it-habitable-for-humans/">Mars</a>. That makes them a good place to study processes that might also happen on other planets. 



Space agencies, such as NASA, need to find resources beyond Earth. Burton’s work may help them plan future missions.



The study also included diagrams that showed how minerals move underground. Water flows below the surface, freezes, and leaves minerals behind. These findings may guide future work in space.



<h2 class="wp-block-heading" id="h-rare-mineral-movement-in-hot-deserts">Rare mineral movement in hot deserts</h2>



Burton’s projects also focus on dry areas in the United States. He studies how minerals move in places like Nevada, Utah, and California’s <a href="https://www.earth.com/news/desert-lichen-may-offer-clues-to-life-beyond-earth/">Mojave Desert</a>. 



These regions are hot, dry, and full of desert basins. The goal is to understand how rare earth elements and lithium move and collect in such places.



Burton described the work as difficult but exciting. "It's a challenge and a scramble, but also very exciting, because there's a lot more for the world to learn in these areas."



<h2 class="wp-block-heading" id="h-a-new-frontier-for-geology">A new frontier for geology</h2>



Montana State University is now focusing more on this type of research. Alison Harmon, vice president for research and economic development at the university, said these studies matter.



"This will be an area where MSU can make an important contribution to national security and economic development in Montana and beyond," said Harmon.



Burton’s research shows that minerals do not stay in one spot forever. Water, ice, and time keep moving them around. By studying how this happens, researchers can learn more about Earth’s resources and even about resources on other worlds.



The study is published in the journal <a href="https://www.sciencedirect.com/science/article/pii/S0165232X25001661?via%3Dihub" target="_blank" rel="noreferrer noopener">Cold Regions Science and Technology</a>.



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Water and ice may reveal where rare earth elements are hiding

We hear about minerals all the time. Lithium, cobalt, nickel,...

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...

Scientists have discovered a rare group of proteins that appear to give microbes in cold environments a strange advantage. These proteins, called cryorhodopsins, respond to light in surprising ways.



Now, researchers think the proteins could be turned into powerful tools for neuroscience and biotechnology.



The icy peaks of the Himalayas, the deep chill of Finnish groundwater, and the ancient glaciers of Greenland all have something in common - they host microscopic life that has adapted to extreme cold.



In doing so, these <a href="https://www.earth.com/news/frozen-worm-comes-back-to-life-after-46000-years/">organisms</a> may have evolved tools that could change how we study and influence the human brain.



<h2 class="wp-block-heading" id="h-unlikely-proteins-found-in-the-cold">Unlikely proteins found in the cold</h2>



It started with a bit of online browsing. While combing through protein databases, a scientist noticed something strange: microbial rhodopsins - proteins usually found in warm, aquatic environments - were popping up in places like <a href="https://www.earth.com/news/safety-on-frozen-lakes-declining-due-to-climate-change/">frozen lakes</a> and glaciers.



Even more oddly, the cold-weather rhodopsins were nearly identical, despite being found in microbes living thousands of kilometers apart. That kind of similarity usually means they serve a crucial function. The team gave them a name to match their habitat: cryorhodopsins.



“In my work, I search for unusual <a href="https://www.earth.com/news/earths-early-life-may-be-a-model-of-alien-life/">rhodopsins</a> and try to understand what they do,” said structural biologist Kirill Kovalev of <a href="https://www.embl.org/">EMBL Hamburg</a>. “Such molecules could have undiscovered functions that we could benefit from.”



<h2 class="wp-block-heading" id="h-searching-for-light-sensitive-proteins">Searching for light-sensitive proteins</h2>



Rhodopsins are light-sensitive proteins. Some of them have already been engineered to act like switches inside cells. 



When exposed to light, they trigger changes in electrical activity. This technique, called optogenetics, is widely used in neuroscience. 



But researchers are still hunting for new types of rhodopsins that could expand the method’s possibilities - especially rhodopsins with different colors, since different wavelengths of light can penetrate biological tissues in different ways.



<h2 class="wp-block-heading" id="h-cold-proteins-change-the-game">Cold proteins change the game</h2>



The cryorhodopsins stood out. Some weren’t the usual orange or pink - they were blue. “I can actually tell what’s going on with cryorhodopsin simply by looking at its color,” said Kovalev.



Using advanced structural biology tools, the team discovered that the same rare structural quirk that first caught their attention also explains why these cryorhodopsins are blue. 



The blue rhodopsins are especially valuable because they can be activated with red light, which travels deeper into tissues and can be used non-invasively.



“Now that we understand what makes them blue, we can design synthetic blue rhodopsins tailored to different applications,” Kovalev said.



<h2 class="wp-block-heading" id="h-light-switches-for-the-brain">Light switches for the brain</h2>



To test whether cryorhodopsins could be useful in optogenetics, the team expressed them in cultured brain cells. The results were exciting. When exposed to <a href="https://www.earth.com/news/some-mammals-have-fur-that-displays-a-striking-glow-under-uv-light/">UV light</a>, the proteins triggered electrical currents. 



Then, depending on the follow-up light exposure - green or red - the cells either became more excitable or less.



“New optogenetic tools to efficiently switch the cell’s electric activity both ‘on’ and ‘off’ would be incredibly useful in research, biotechnology and medicine,” said Tobias Moser of the University Medical Center Göttingen.



“For example, in my group, we develop new optical cochlear implants for patients that can optogenetically restore <a href="https://www.earth.com/news/drugs-may-be-available-to-prevent-hearing-loss/">hearing</a> in patients. Developing the utility of such a multi-purpose rhodopsin for future applications is an important task for the next studies.”



According to Kovalev, the cryorhodopsins aren’t ready to be used as tools yet, but they’re an excellent prototype. "They have all the key features that, based on our findings, could be engineered to become more effective for optogenetics."



<h2 class="wp-block-heading" id="h-sensing-more-than-just-light">Sensing more than just light</h2>



The surprises didn’t stop there. Researchers at Goethe University Frankfurt tested cryorhodopsins and found something unusual. These proteins are the slowest of all known rhodopsins when responding to light - and they’re sensitive to UV.



That slowness might be a feature, not a bug. It could let microbes “see” UV light, which would be a first. UV radiation is especially intense in high-altitude or polar environments. Being able to sense radiation might help microbes protect themselves.



However, the question remained: can microbes actually sense UV light? The search for an answer led the team to a genetic mystery. 



<h2 class="wp-block-heading" id="h-discovery-of-tiny-unknown-proteins">Discovery of tiny, unknown proteins</h2>



The cryorhodopsin gene always came packaged with another gene encoding a small, unknown protein. The team suspected it might be a messenger - a partner protein that helps transmit the UV light signal inside the cell.



Using the AI tool AlphaFold, the researchers predicted that five copies of the tiny protein form a ring that hugs the cryorhodopsin from the inside. 



When the rhodopsin detects UV light, the small protein might break off and carry the signal further into the cell.



"It was fascinating to uncover a new mechanism via which the light-sensitive signal from cryorhodopsins could be passed on to other parts of the cell. It is always a thrill to learn what the functions are for uncharacterized proteins," noted the researchers.



"In fact, we find these proteins also in organisms that do not contain cryorhodopsin, perhaps hinting at a much wider range of jobs for these proteins.”



<h2 class="wp-block-heading" id="h-proteins-didn-t-evolve-due-to-cold">Proteins didn't evolve due to cold</h2>



While the full picture isn’t clear yet, the researchers have a strong hunch. Kovalev said the team suspects that cryorhodopsins evolved their <a href="https://www.earth.com/news/new-shape-shifting-proteins-open-doors-in-medicine-and-farming/">unique features</a> not because of the cold, but rather to let microbes sense UV light, which can be harmful to them.



“In cold environments, such as the top of a mountain, bacteria face intense UV radiation. Cryorhodopsins might help them sense it, so they could protect themselves. This hypothesis aligns well with our findings," noted Kovalev.



“Discovering extraordinary molecules like these wouldn’t be possible without scientific expeditions to often remote locations, to study the adaptations of the organisms living there. We can learn so much from that!”



Cryorhodopsins aren’t ready to be used in the lab or the clinic just yet, but they are a solid starting point. Ultimately, they might offer a way to sense UV light inside of living cells. 



The proteins could also serve as new light-controlled tools for brain research, precision medicine, or even advanced prosthetics.



The full study was published in the journal <a href="https://www.science.org/doi/10.1126/sciadv.adv1015">Science Advances</a>.



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Can we control brain cells with light? New clues from frozen proteins

Scientists have discovered a rare group of proteins that appear...

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)...

The,Girl,Looks,Through,A,Night,Vision,Device,In,The

Night vision gear keeps soldiers and rescuers safe after sundown, yet the gear’s size and weight strain necks and pack <a href="https://www.earth.com/news/scientists-detect-more-than-20-mysterious-radio-signals-from-space/">space</a>. A Boston research team says that problem might soon end thanks to a heat sensor that is made from a new ultra‑thin film.



Conventional goggles rely on HgCdTe sensors that must be chilled with liquid nitrogen to hush electronic noise, and the cooling units alone can weigh several pounds. That heft discourages use outside the military and drives up costs.



Materials engineer <a href="https://mit.academia.edu/XinyuanZhang" target="_blank" rel="noreferrer noopener">Xinyuan Zhang</a> of the Massachusetts Institute of Technology (<a href="https://www.mit.edu/" target="_blank" rel="noreferrer noopener">MIT</a>) leads the study, working with collaborators from <a href="https://www.rpi.edu/" target="_blank" rel="noreferrer noopener">Rensselaer</a> and <a href="https://en.snu.ac.kr/" target="_blank" rel="noreferrer noopener">Seoul National University</a>.



<h2 class="wp-block-heading" id="h-cooling-with-no-coolers">Cooling with no coolers</h2>



<a href="https://www.rp-photonics.com/pyroelectric_detectors.html" target="_blank" rel="noreferrer noopener">Pyroelectric detectors</a> respond to temperature swings instead of individual photons, but random <a href="https://journals.aps.org/prb/abstract/10.1103/PhysRevB.106.L201409" target="_blank" rel="noreferrer noopener">atomic motion</a> often drowns their signals. 



Zhang’s group tackled that noise by trimming the active layer to ten‑nanometer sheets, thin enough to quiet internal chatter yet sturdy enough to handle field duty.



The sheets are made from 'pyroelectric lead magnesium niobate‑lead titanate,' better known as <a href="https://www.sciencedirect.com/science/article/abs/pii/S0924424710003201">PMN‑PT</a>, a crystal already prized for sonar transducers and actuators. 



At room temperature a stack of one hundred sheets outperformed the chilled benchmark across the full far‑infrared band, something no uncooled sensor has done before.



<h2 class="wp-block-heading" id="h-atomic-lift-off-on-a-chip">Atomic lift‑off on a chip</h2>



The team achieved those sheets with a process called atomic lift‑off, which peels a finished crystal from its growth wafer without an intermediate release layer. Remote epitaxy, the older alternative, uses <a href="https://www.earth.com/news/graphene-wonder-material-changing-the-world-is-officially-declared-safe-for-humans/">graphene</a> as a sacrificial buffer and adds cost and time.



“We just had to exert a bit of stress to induce a crack at the interface between the film and the substrate and we could realize the liftoff,” said Zhang. 



Lead atoms inside PMN‑PT weaken bonds at the crystal–substrate interface, so a gentle nick lets the film pop free intact. 



That trick sidesteps the spalling damage that plagues other lift‑off attempts and delivers atom‑smooth membranes ready for transfer. 



Because the sheets come loose in seconds and need neither chemical etching nor exotic buffers, the manufacturing route scales to full‑wafer panels, opening the door to high‑pixel‑count arrays.



<h2 class="wp-block-heading" id="h-thinner-films-better-sensors">Thinner films, better sensors</h2>



One of the ultrathin <a href="https://www.researchgate.net/publication/231073910_Investigation_of_the_electrical_properties_of_1_-_XPbMg_13Nb23O3-xPbTiO3_single_crystals_with_special_reference_to_pyroelectric_detection" target="_blank" rel="noreferrer noopener">films</a>, just ten nanometers thick, showed a sensitivity far beyond older materials used in thermal sensors. 



It picked up heat changes more than 100 times better than some standard options, while working across a wider range of infrared light that traditional detectors can’t see without heavy cooling systems.



“We were trying to achieve performance comparable with cooled detectors,” said Zhang. 



In lab tests, the film detected tiny temperature shifts, small enough to outline a person from several football fields away in complete darkness. The chip beneath processed the signals without needing extra power-hungry parts.



<h2 class="wp-block-heading" id="h-beyond-the-battlefield">Beyond the battlefield</h2>



Lightweight thermal “specs” could help firefighters navigate smoke, electrical workers check live lines, and wildlife biologists count animals after dusk. 



<a href="https://techxplore.com/news/2024-10-infrared-camera-aims-safety-autonomous.html" target="_blank" rel="noreferrer noopener">Automakers</a> watch the work closely because infrared cameras improve pedestrian detection when headlights glare or fog rolls in. 



A fingernail‑size uncooled sensor could slide behind the windshield without affecting dashboard design.



Orbiting <a href="https://geoxc-apps.bd.esri.com/space/satellite-explorer/" target="_blank" rel="noreferrer noopener">satellites</a> might pack dozens of the chips for high‑resolution climate mapping, while a stretchable version could monitor skin temperature on smartwatches.



<h2 class="wp-block-heading" id="h-room-temperature-reliability">Room-temperature reliability</h2>



To see how the material might perform outside the lab, Zhang’s team built a small heat-sensing chip using slightly thicker versions of the film. 



Every part of the array worked, and the <a href="https://www.earth.com/news/new-sensor-remotely-tracks-plant-health-in-real-time/">sensors</a> gave steady, reliable readings across the entire surface.



These test chips were even more sensitive than standard materials used today. 



Unlike traditional sensors that need to be chilled and still miss parts of the heat spectrum, this new film worked at room temperature and picked up the full range of heat signals.



<h2 class="wp-block-heading" id="h-early-production-hurdles">Early production hurdles</h2>



Despite the promising performance, device fabrication from the thinnest membranes still poses reliability issues. 



While 80-nanometer membranes yielded consistent devices across the array, only about 20 percent of the 10-nanometer devices survived handling during transfer and integration.



Zhang’s team is working on process improvements, including protective coatings and automation tools to reduce membrane breakage. 



These upgrades aim to make ultrathin sheets more viable for commercial production and large-area sensor arrays in industrial and <a href="https://www.earth.com/news/what-was-it-doing-u-s-space-plane-returns-after-14-mysterious-months/">military</a> settings.



<h2 class="wp-block-heading" id="h-steps-still-ahead">Steps still ahead</h2>



The film itself is thinner than a red blood cell, yet lenses, read‑out circuits, and batteries still need space. Zhang’s group is redesigning optics to funnel heat onto postage‑stamp detectors rather than inch‑wide arrays.



“I think night‑vision contact lenses will be challenging to build, but I expect our technology could potentially be used to make something that looks like normal spectacles,” Zhang said. 



Further studies aim to replace lead with less toxic elements and to test the lift‑off trick on other ferroelectrics, which could lower environmental impact and diversify applications.



The study is published in <a href="https://www.nature.com/articles/s41586-025-08874-7" target="_blank" rel="noreferrer noopener">Nature</a>.



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New ultrathin material set to replace bulky night-vision goggles

Night vision gear keeps soldiers and rescuers safe after sundown,...

A quick text that says “thinking of you” might seem trivial, yet these small gestures can quietly shift our own mood. A month‑long study tracking daily life revealed that people who expressed love were more likely to rate themselves as <a href="https://www.earth.com/news/people-are-falling-in-love-with-ai-companions-and-it-could-be-dangerous/">loved</a> in the hours that followed.



This loop between giving and receiving affection was uncovered by a research team led by Dr. Zita Oravecz at <a href="https://www.psu.edu/">Pennsylvania State University</a>.



<h2 class="wp-block-heading" id="h-small-acts-express-love">Small acts express love </h2>



Social psychologist Dr. Barbara Fredrickson of <a href="https://www.google.com/search?q=University+of+North+Carolina+at+Chapel+Hill&amp;client=ms-android-charter-us-rvc3&amp;sourceid=chrome-mobile&amp;ie=UTF-8#ebo=0">UNC Chapel Hill</a> calls these shared moments <a href="https://www.themarginalian.org/2013/01/28/love-2-0-barbara-fredrickson/" target="_blank" rel="noreferrer noopener">positivity resonance</a>. She describes love as “micro‑moments of warmth and connection” that feel the same whether they happen with a stranger or a soul mate.



By focusing on brief interactions rather than grand declarations, her framework reminds us that <a href="https://www.earth.com/news/why-our-relationships-with-dogs-matter-so-much/">love</a> is accessible dozens of times a day.



Those flashes of connection line up with the <a href="https://www.authentichappiness.sas.upenn.edu/" target="_blank" rel="noreferrer noopener">Penn State</a> finding that even modest acts, like holding a door or sending a supportive emoji, can echo back for hours. 



Because the feeling is mutual and momentary, the cost of entry is low, but the psychological payoff is high.



<h2 class="wp-block-heading" id="h-daily-love-and-feelings">Daily love and feelings</h2>



The researchers used <a href="https://pubmed.ncbi.nlm.nih.gov/18509902/" target="_blank" rel="noreferrer noopener">ecological momentary assessment</a> to ping 52 adults six times daily for four weeks, asking how much love they had expressed since the last alert and how loved they felt right then. 



The participants slid a marker from 0 to 100 on each question, producing nearly 8,200 observations for analysis.



A continuous‑time model showed that felt love stayed elevated far longer than the urge to <a href="https://www.earth.com/news/some-people-are-born-to-enjoy-music-more-than-others/">express</a> it; in statistical terms, its inertia remained strong even eight hours later. 



Expressed love, by contrast, faded quickly, hinting that we need to keep showing up if we want the warm glow to persist.



<h2 class="wp-block-heading" id="h-expressing-love-makes-you-feel-loved-nbsp">Expressing love makes you feel loved&nbsp;</h2>



Numbers told the clearest story: a spike in expressed love predicted a later bump in felt <a href="https://www.earth.com/news/oxytocin-cuddle-hormone-fosters-love-boosts-memory-and-may-cure-addiction/">love</a>, peaking about three hours after the gesture. However, a surge in feeling loved did not reliably spark new expressions outward.



“Let’s spread more love in the world by expressing love throughout our daily lives,” said the researchers.



The asymmetry suggests that taking the first step matters more than waiting to be inspired by someone else’s kindness.



<h2 class="wp-block-heading" id="h-feeling-loved-lasts-after-expressing-it">Feeling loved lasts after expressing it</h2>



Felt love’s staying power linked strongly to flourishing, a broad gauge of purpose, relationships, and optimism measured with the <a href="https://ggsc.berkeley.edu/images/uploads/The_Subjective_Happiness_Scale.pdf" target="_blank" rel="noreferrer noopener">Diener Flourishing Scale</a>. 



People whose loving feelings decayed slowly also scored higher on subjective happiness, echoing prior work showing that secure social bonds shield against stress and loneliness.



Because the emotional state lasts, a single morning compliment can quietly steer the rest of the day. The model implies a simple arithmetic: every extra act you offer raises the baseline from which later mood unfolds.



<h2 class="wp-block-heading" id="h-love-improves-health-and-happiness">Love improves health and happiness</h2>



“These benefits happen when affection is expressed, not merely felt,” said Kory Floyd, professor at Arizona State University.



Professor Floyd <a href="https://news.asu.edu/content/study-expressing-love-can-improve-your-health" target="_blank" rel="noreferrer noopener">found</a> that kissing lowered cholesterol, decreased cortisol, and boosted relationship satisfaction. 



Other <a href="https://pubmed.ncbi.nlm.nih.gov/15740822/" target="_blank" rel="noreferrer noopener">studies</a> link affectionate touch with higher oxytocin, lower blood pressure, and faster recovery from acute stress, reinforcing the biological logic behind the Penn State data.



Stacked together, the evidence recasts love as a preventive health behavior rather than a soft emotion. Doctors can’t prescribe it in a bottle, yet a polite note or gentle squeeze may rival many over‑the‑counter remedies.



<h2 class="wp-block-heading" id="h-ways-to-express-love-in-daily-life">Ways to express love in daily life</h2>



Putting the findings into practice begins with noticing small moments - a barista’s name tag, a co-worker’s quiet contribution, or a relative’s favorite song on the radio. 



Turning that recognition into a kind word, gesture, or small favor can plant a seed that often blooms later in the day.



Because the loop begins with behavior, it sidesteps the trap of waiting until you “feel like it.” 



Habitual practice trains attention to catch more of Dr. Fredrickson’s micro‑moments, which in turn widens the field for the next act of love.



<h2 class="wp-block-heading" id="h-love-exists-beyond-romance">Love exists beyond romance</h2>



Although many associate love with romantic partners, the study didn’t limit its scope to couples. Participants reported loving exchanges across a range of relationships, including friends, family, coworkers, and even strangers.



Other studies have demonstrated that people commonly recognize small acts from anyone, like a kind word from a passerby, as ways to express and feel real love. 



The study suggests that everyday expressions of love aren't limited to close relationships - they’re woven into many forms of human connection.



The study is published in the journal <a href="https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0323326" target="_blank" rel="noreferrer noopener">PLOS One</a>.



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Small acts of love might be the key to feeling loved

A quick text that says “thinking of you” might seem...

Some species of fig trees possess an extraordinary ability. They can store calcium carbonate inside their trunks, essentially turning parts of themselves into stone. 



A new study shows that these <a href="https://www.earth.com/news/tropical-tree-deaths-are-increasing-even-in-untouched-forests/">trees</a> absorb carbon dioxide from the air and lock it away as calcium carbonate rocks in the surrounding soil.



This surprising discovery comes from an international team of scientists from Kenya, the U.S., Austria, and Switzerland. The experts presented their research at the <a href="https://conf.goldschmidt.info/goldschmidt/2025/meetingapp.cgi" target="_blank" rel="noreferrer noopener">Goldschmidt Conference</a> in Prague.



<h2 class="wp-block-heading" id="h-how-fig-trees-store-carbon">How fig trees store carbon</h2>



These fig trees, which naturally grow in Kenya, are among the first known fruit-bearing trees to use a process called the oxalate carbonate pathway. This process plays a unique role in how these trees manage carbon from the atmosphere. 



Like most <a href="https://www.earth.com/news/tree-species-face-unprecedented-climate-shifts-across-their-ranges/">trees</a>, they absorb carbon dioxide from the air during photosynthesis. They then convert this carbon dioxide into organic carbon, which helps the trees grow. 



The carbon becomes part of their physical structures, including their leaves, roots, branches, and trunks. This is a common way in which trees capture and store carbon.



However, the trees have an additional, remarkable ability. Besides storing carbon in their leaves and wood, they also produce special crystals made from a compound called calcium oxalate.



Over time, the calcium oxalate crystals break down and change into calcium carbonate. Calcium carbonate is a mineral found in natural substances like chalk, limestone, and seashells. It has the ability to stay locked in the soil for a much longer time than regular organic carbon.



<h2 class="wp-block-heading" id="h-benefits-of-carbon-storage">Benefits of carbon storage</h2>



This process provides two major benefits. First, it keeps carbon locked away in a stable, mineral form, reducing the amount of carbon dioxide that might return to the atmosphere. 



Second, the formation of calcium carbonate raises the pH of the soil, making it less acidic. This change in the soil’s chemistry improves the availability of certain nutrients, making the surrounding environment healthier for plants and soil organisms.



In simple terms, these fig <a href="https://www.earth.com/news/climate-change-is-disrupting-how-amazon-trees-process-sunlight/">trees</a> not only store carbon inside their wood but also help improve the soil while trapping carbon in a long-lasting, stone-like form.



<h2 class="wp-block-heading" id="h-fig-trees-lock-carbon-in-their-trunks">Fig trees lock carbon in their trunks</h2>



The study's findings were presented by Dr. Mike Rowley, a senior lecturer at the <a href="https://www.uzh.ch/en.html" target="_blank" rel="noreferrer noopener">University of Zurich</a>.



“We’ve known about the oxalate carbonate pathway for some time, but its potential for sequestering carbon hasn’t been fully considered," explained Dr. Rowley.



"If we’re planting trees for agroforestry and their ability to store CO2 as organic carbon, while producing food, we could choose trees that provide an additional benefit by sequestering inorganic carbon also, in the form of calcium carbonate."



The researchers studied three types of fig trees in Samburu County, Kenya. They measured how far calcium carbonate forms from the trees and examined the microbial communities involved in this transformation.



<h2 class="wp-block-heading" id="h-carbon-storage-inside-tree-wood">Carbon storage inside tree wood</h2>



The team used advanced techniques at the <a href="https://www-ssrl.slac.stanford.edu/ssrl/web/" target="_blank" rel="noreferrer noopener">Stanford Synchrotron Radiation Lightsource</a>. They discovered calcium carbonate deposits both on the tree bark and deep inside the wood.



Dr. Rowley noted that the calcium carbonate is formed, the soil around the tree becomes more alkaline. 



"The calcium carbonate is formed both on the surface of the tree and within the wood structures, likely as microorganisms decompose crystals on the surface and also, penetrate deeper into the tree," said Dr. Rowley.



"It shows that inorganic carbon is being sequestered more deeply within the wood than we previously realized."



Among the fig trees studied, Ficus wakefieldii showed the highest ability to store carbon in this way. Next, the researchers plan to test its suitability for agroforestry by measuring its water needs, fruit production, and <a href="https://www.earth.com/news/amazon-trees-glow-more-under-stress-but-photosynthesize-less/">carbon</a> storage under varying conditions.



<h2 class="wp-block-heading" id="h-implications-for-other-tree-species">Implications for other tree species </h2>



Previous studies on the oxalate carbonate pathway focused mostly on tropical trees that do not bear fruit. The Iroko tree, or Milicia excelsa, was the first identified species with this pathway. It can store up to one ton of calcium carbonate during its life.



Calcium oxalate, which forms these crystals, is common in many plants. Likewise, the microorganisms that convert it to calcium carbonate live in many soils.



“It’s easier to identify calcium carbonate in drier environments. However, even in wetter environments, the carbon can still be sequestered," noted Dr. Rowley.



"So far, numerous species of tree have been identified which can form calcium carbonate. But we believe there are many more." 



"This means that the oxalate-carbonate pathway could be a significant, underexplored opportunity to help mitigate CO2 emissions as we plant trees for forestry or fruit."



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How fig trees turn parts of themselves to stone

Some species of fig trees possess an extraordinary ability. They...

Everyone sends texts. It’s simple - one message goes out, another comes back. Somewhere in between, emojis appear. They smile, wink, cry. Without much notice, emojis change how messages feel.



Researchers often ignore these tiny icons. But Eun Huh from the <a href="https://www.utexas.edu" target="_blank" rel="noreferrer noopener">University of Texas at Austin</a> decided to take a closer look. Her study asks a simple question: do emojis make people feel closer in their <a href="https://www.earth.com/news/sending-the-right-message-emojis-can-be-misinterpreted/">relationships</a>?



"The study revealed that emojis can boost relationship satisfaction by signaling emotional attentiveness. Interestingly, it's not the type of emoji but simply their presence that makes people feel closer to their partner," noted Huh.



<h2 class="wp-block-heading" id="h-emojis-change-how-texts-feel">Emojis change how texts feel</h2>



Think about your last text. Did it have an emoji? Most likely it did. Nearly everyone uses them.



But emojis aren’t just decorations. They work like tiny signals of <a href="https://www.earth.com/news/the-way-you-send-emojis-shows-your-attachment-style/">emotion</a> and bring life to plain words. A simple thumbs-up or heart can completely change a the mood of a message.



The researchers looked at this effect closely. Their analysis showed something surprising. People feel more connected to those who use emojis. It’s not about picking the right emoji. The magic lies in using them at all.



<h2 class="wp-block-heading" id="h-emojis-make-relationships-feel-closer">Emojis make relationships feel closer</h2>



The researchers asked 260 adults to imagine texting close friends. They read 15 different chat examples. Some had emojis, while others didn’t.



The results were clear. People trusted emoji users more. They called them more responsive and the chats felt warmer.



Surprisingly, the type of emoji didn’t matter - faces, hearts, or objects made no difference. What mattered was simply that an emoji was there at all.



<h2 class="wp-block-heading" id="h-making-messages-feel-human">Making messages feel human</h2>



Text without emotion can feel cold. Emojis fix that. They help <a href="https://www.earth.com/news/older-adults-often-understand-emojis-but-hesitate-to-use-them/">messages</a> feel personal, soften harsh words, and make it easier to spot the sender’s true feelings.



Our brains react to emojis just like they do to real human faces. That’s not just a guess - it’s been measured. These icons tap into deep emotional areas in the mind.



Emojis also work fast. They don’t need long explanations. A simple symbol gets the message across instantly.



<h2 class="wp-block-heading" id="h-emojis-help-people-feel-heard">Emojis help people feel heard</h2>



Responsiveness may be the element that boosts a feeling of connectedness. In every case, people felt more heard when <a href="https://www.earth.com/news/ai-does-not-replace-human-creativity-but-enhances-it/">messages</a> included emojis. That sense of being heard led to stronger friendships.



The researchers ran more tests to dig deeper. They found that emojis didn’t boost likability or closeness on their own. Instead, emojis made people feel listened to. That feeling then brought everything else - friendship, closeness, and satisfaction.



<h2 class="wp-block-heading" id="h-matching-emojis-boost-connections">Matching emojis boost connections</h2>



The study controlled the message tone carefully. The researchers didn’t want sarcastic jokes throwing off the results.



Positive emojis appeared with positive text. Sad emojis came with sad words. This made sure the emotional flow stayed clear. 



Even with this careful setup, the study proved its point. People felt emotionally connected when emojis matched the message.



But here’s the best part: the type of emoji still didn’t matter. Any emoji could spark the same emotional effect.



<h2 class="wp-block-heading" id="h-emojis-fix-tone-and-avoid-confusion">Emojis fix tone and avoid confusion</h2>



Why do emojis work so well? They make conversations feel softer and friendlier. A simple smiley face can take the edge off a blunt reply. 



Emojis can help to reduce misunderstandings, since tone gets tricky over text. Emojis also act like little bursts of warmth. They draw attention and show effort, even in rushed conversations. 



Most importantly, emojis can do what words sometimes can’t - show that you care.



<h2 class="wp-block-heading" id="h-growing-digital-friendships">Growing digital friendships</h2>



This study offers a simple truth: emojis make people feel closer. You don’t need to think hard about which emoji to use. Just adding one makes a difference. 



In a world where everyone is busy, emojis are shortcuts to emotional connection. They don’t take much time. But they pack a punch. 



Emojis turn plain chats into something more meaningful. They remind people that someone is paying attention.



<h2 class="wp-block-heading" id="h-further-studies-are-needed">Further studies are needed</h2>



Of course, every study has limitations. This one focused on imagined situations. People weren’t texting real friends during the test. The researchers suggest testing real-time chats next.



The experts pointed out that this study included mostly U.S.-based participants. Emoji meanings can shift across cultures. What works in one place might not in another.



And there’s one more question waiting. What happens when emojis clash with words? Like a smiley face paired with sad news. Future studies might explore those mixed signals.



<h2 class="wp-block-heading" id="h-emojis-and-relationship-satisfaction">Emojis and relationship satisfaction </h2>



In the end, this study reveals something many miss. Emojis are not just fun add-ons. They act as emotional glue in text messages.



They help people feel seen, make replies feel warmer, and pull friendships a little closer.



"The study revealed that emojis can boost relationship satisfaction by signaling emotional attentiveness," said Huh. "Interestingly, it's not the type of emoji but simply their presence that makes people feel closer to their partner."



The study is published in the journal <a href="https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0326189" target="_blank" rel="noreferrer noopener">PLOS One</a>.



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Emojis help people feel closer in their relationships

Everyone sends texts. It’s simple - one message goes out,...

A pulsing headache can feel like your brain is fighting for space. New research suggests that this tug-of-war may trace back to Neanderthal skull traits we share with our extinct cousins.



A recent study zeroes in on Chiari malformation type 1, a condition in which the lower <a href="https://www.ncbi.nlm.nih.gov/books/NBK538167/" target="_blank" rel="noreferrer noopener">cerebellum</a> droops through the foramen magnum, the bony opening at the skull’s base.



Lead author Kimberly Plomp of the <a href="https://upd.edu.ph" target="_blank" rel="noreferrer noopener">University of the Philippines Diliman</a> teamed up with neurosurgeon Yvens Barbosa Fernandes from Brazil’s <a href="https://unicamp.br/en/" target="_blank" rel="noreferrer noopener">State University of Campinas</a> to test an idea he floated in 2013.



<h2 class="wp-block-heading" id="h-neanderthal-skull-shape-squeezes-the-brain">Neanderthal skull shape squeezes the brain</h2>



Surgeons diagnose <a href="https://www.ninds.nih.gov/chiari-malformation-fact-sheet" target="_blank" rel="noreferrer noopener">Chiari</a> after spotting a compressed cerebellum on MRI scans, but the root cause has stayed murky. Scientists estimate that type 1 affects about one in every 100 Americans.



The new modeling work confirms that people with Chiari share a smaller, flatter <a href="https://bvajournals.onlinelibrary.wiley.com/doi/10.1136/inp.m1869" target="_blank" rel="noreferrer noopener">occipital bone</a> than unaffected <a href="https://www.earth.com/news/scientists-inject-40000-year-old-neanderthal-dna-gli3-gene-into-mice-with-incredible-results/">peers</a>. That subtle tilt reduces the bony cradle that normally cups the cerebellum and keeps it clear of the spinal canal.



“It makes sense, if you have less angulation, you have less space for the modern <a href="https://www.earth.com/news/neanderthal-superhighways-through-eurasia-recreated-with-supercomputers/">human</a> brain,” said Barbosa Fernandes at the end of surgery rounds. He first noticed the resemblance while examining museum casts of ancient skulls during a European trip.



Headaches are common, yet <a href="https://www.aans.org/Patients/Neurosurgical-Conditions-and-Treatments/Chiari-Malformation" target="_blank" rel="noreferrer noopener">Chiari</a> pain often flares when coughing, straining, or even laughing. Other symptoms range from neck pain to tingling hands, and some cases stay silent for years.



<h2 class="wp-block-heading" id="h-neanderthal-skull-shape-linked-to-brain-condition">Neanderthal skull shape linked to brain condition</h2>



Plomp’s team built digital 3‑D models of 46 Chiari skulls and 57 controls from hospital CT scans, then compared them to eight fossil crania. 



The Chiari group <a href="https://academic.oup.com/emph/advance-article/doi/10.1093/emph/eoaf009/8175225" target="_blank" rel="noreferrer noopener">matched</a> Homo neanderthalensis almost point for point, while Homo erectus, Homo heidelbergensis, and early Homo sapiens aligned with today’s rounder <a href="https://www.earth.com/news/neanderthal-fossils-reveal-signs-of-a-population-collapse/">skulls</a>.



“It highlights the idea that these are Neanderthal traits, not just early traits,” said Plomp, her screen filled with color‑coded heat maps of bone angles. She called the overlap “another way that Neanderthal genes might be influencing our health, and in this case, in a negative way.”



Neanderthals carried brains slightly larger than ours, but their cranial base sloped backward like a built‑in ramp. That shape fits an ice‑age life of powerful jaw muscles and big sinus spaces, yet it also left scant room for a bulging <a href="https://www.earth.com/news/new-theory-explains-why-neanderthals-vanished-and-homo-sapiens-are-alive-today/">human</a> cerebellum.



Most people carry between 1 and 2 percent <a href="https://www.nature.com/articles/nature12961" target="_blank" rel="noreferrer noopener">Neanderthal DNA</a>, a legacy of interbreeding roughly 50,000 years ago. Much of that genetic cargo is benign, though some alleles affect immune response, metabolism, and now, it seems, skull geometry.



<h2 class="wp-block-heading" id="h-ancient-neanderthal-dna-and-skull-shape">Ancient Neanderthal DNA and skull shape</h2>



The overlap does not prove cause and effect, so the team now plans full‑genome scans of Chiari patients to hunt “introgressed” sequences, bits of archaic DNA that slipped into the modern gene pool. 



Introgression <a href="https://pubmed.ncbi.nlm.nih.gov/36763080/" target="_blank" rel="noreferrer noopener">studies</a> have already linked certain Neanderthal variants to nicotine addiction and even severe COVID‑19 cases.



If a skull‑shaping gene set turns up, clinicians could screen high‑risk families before symptoms strike. Early detection matters because decompression surgery, while effective, involves removing bone and sometimes fusing vertebrae.



“I didn’t have the science to prove my hypothesis. This paper is a big step closer toward that proof,” said Barbosa Fernandes after reviewing the metric curves.



Other forms of Chiari, labeled types 2 through 4, follow different rules. Type 2, in contrast, is tightly linked to severe <a href="https://www.spinabifidaassociation.org/" target="_blank" rel="noreferrer noopener">spina bifida</a>.



<h2 class="wp-block-heading" id="h-how-skull-shape-affects-daily-life">How skull shape affects daily life</h2>



The cerebellum fine‑tunes balance, speech, and motor control, so its squeeze can scramble day‑to‑day skills such as handwriting or climbing stairs. 



MRI technicians now know to look for the tell‑tale “tonsillar descent,” a downward bulge of cerebellar tissue past the foramen magnum.



Many patients report that lying flat eases pressure, hinting that gravity exacerbates the pinch. Others seek help only after years of unexplained migraines, an example of how ancient traits can hide in plain sight.



Anthropologists see the study as proof that evolutionary leftovers do not always vanish quietly. A skull optimized for an Ice Age hunter may pose problems for a modern desk worker whose brain spends hours hunched over screens. 



Pediatric surgeons are also watching. If Neanderthal‑linked genes surface, prenatal scans may one day flag a risky skull angle long before birth.



<h2 class="wp-block-heading" id="h-predicting-brain-conditions">Predicting brain conditions</h2>



Plomp’s group now collaborates with population geneticists to map their CT findings onto hundreds of living genomes. They hope to learn whether carriers of specific Neanderthal skull DNA face higher odds of surgical intervention.



Public health officials could then estimate regional Chiari burdens and tailor neurosurgery training programs. In areas with limited MRI access, a simple cranial X‑ray angle might serve as an early warning.



Evolution offers trade‑offs, and the Neanderthal‑style skull saved heat in bitter winters but became a tight squeeze for our expanded cerebellum. Knowing that trade‑off exists empowers clinicians and patients alike.



“It looks like this is just another way that Neanderthal genes might be influencing our health, and in this case, in a negative way,” said Plomp. The team hopes DNA data will seal the evolutionary link.



The study is published in the journal <a href="https://academic.oup.com/emph/advance-article/doi/10.1093/emph/eoaf009/8175225?login=false" target="_blank" rel="noreferrer noopener">Evolution, Medicine, and Public Health</a>.



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Neanderthal skull traits cause modern human brain problems

A pulsing headache can feel like your brain is fighting...

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...

Sexual behavior and preference - whether in humans or animals - isn’t random. It’s shaped early on, during fetal development, by how the brain responds to hormones like androgens (male sex hormones). 



This early exposure is known to affect many important adult traits. But there's been one big obstacle: how do you measure that influence without invasive methods?



<h2 class="wp-block-heading" id="h-rat-fingers-hint-at-sexual-behavior">Rat fingers hint at sexual behavior </h2>



Researchers from <a href="https://www.okayama-u.ac.jp/index_e.html" target="_blank" rel="noreferrer noopener">Okayama University</a> in Japan may have found an answer - by looking at rats’ fingers.



In a recent study, a team led by Professor <a href="https://loop.frontiersin.org/people/32931/overview" target="_blank" rel="noreferrer noopener">Hirotaka Sakamoto</a> and Dr. Himeka Hayashi found that a simple finger measurement - the ratio of the second digit to the fourth digit, known as 2D:4D - can predict sexual behavior and preference in rats.



This digit ratio has been studied in humans for years. On average, men tend to have a lower 2D:4D ratio than women, meaning their index fingers are shorter relative to their ring fingers. 



But surprisingly, there hasn’t been much research testing whether this holds true in other animals, nor has sexual proclivity been measured against 2D:4D ratio in humans or other animals. That’s what drew the researchers to rats.



<h2 class="wp-block-heading" id="h-understanding-the-2d-4d-ratio">Understanding the 2D:4D ratio</h2>



As stated, the 2D:4D ratio compares the lengths of your index finger (2D) and your ring finger (4D). 



To find it, just look at your right hand: if your ring finger is longer than your index finger, your 2D:4D ratio is considered low; if your index finger is about the same length or longer, your ratio is higher. 



Scientists have found that this ratio is set before you're born, influenced by the amount of <a href="https://www.earth.com/news/men-with-low-testosterone-have-a-higher-risk-of-mortality/">testosterone</a> and <a href="https://www.earth.com/news/study-suggests-menopause-can-be-delayed-or-even-eliminated/">estrogen</a> you were exposed to in the womb. 



In general, people with lower ratios were exposed to more testosterone, while higher ratios suggest more estrogen exposure.



This tiny finger difference has caught scientists’ attention because it seems to connect to traits like athletic ability, aggression, risk-taking, and even career interests. 



For example, some studies have found that people with lower 2D:4D ratios tend to do better in competitive sports or lean toward science and engineering fields. 



It’s also been tied to traits like <a href="https://www.earth.com/news/practicing-yoga-nidra-improves-sleep-memory-and-cognition/">cognition</a>, <a href="https://www.earth.com/news/personality-traits-are-not-strongly-inherited-from-parents/">personality</a>, <a href="https://www.earth.com/news/lack-of-sexual-satisfaction-linked-to-rapid-memory-decline/">sex drive</a>, and even <a href="https://www.earth.com/news/same-sex-sexual-behavior-linked-to-evolutionary-advantages-in-monkeys/">sexual orientation</a>.



But it’s not a rule - it’s just a pattern seen in large groups, not a way to predict someone’s future.



<h2 class="wp-block-heading" id="h-shorter-fingers-stronger-sex-drive">Shorter fingers, stronger sex drive</h2>



“We found that the 2D:4D ratio serves as a reliable biological marker for predicting sexual activity in rats,” said Sakamoto. 



“Rats with shorter second digits were not only more sexually active but also showed a clear preference for female scent.”



Building on their initial measurements, the team then ran mating trials to observe <a href="https://www.earth.com/news/science-behind-predicting-and-changing-human-behavior/">behavior</a>.



The results were clear. Male rats that ejaculated during their first encounter had shorter second digits compared to those that didn’t. 



These males also showed signs of higher sexual drive: they ejaculated more often, did so more quickly, and had stronger erectile function.



<h2 class="wp-block-heading" id="h-the-scent-of-sexual-behavior">The scent of sexual behavior </h2>



To go beyond behavior and look at preference, the researchers ran a simple but telling test. They placed male rats in a cage with two kinds of bedding: one scented by females, and the other by males.



All the male rats initially explored the male-scented bedding. But only those with shorter second digits stayed interested in the female-scented bedding. They sniffed, explored, and spent more time with it - indicating a clear sexual preference.



“While most studies have only linked the digit ratio to morphological sex differences, we noticed a surprising lack of research connecting digit ratio to the biological basis of sex itself - especially sexual activity and preference,” notes Hayashi. “This curiosity marked the start of our study.”



<h2 class="wp-block-heading" id="h-fingers-mirror-brain-wiring">Fingers mirror brain wiring</h2>



Beyond offering insight into rat behavior, the study points to a deeper question: how early hormone exposure shapes the brain in lasting ways.



Before birth, hormone exposure might wire our brains in ways that the 2D:4D ratio later reflects - potentially shaping complex behaviors like sexual orientation or emotional attachment.



“Our results suggest a profound link between the body and mind, with significant scientific and clinical implications,” said Sakamoto. “Simply examining our fingers could one day help identify aspects of our behavioral tendencies.”



The findings also offer a practical model for exploring biological questions that are difficult - or impossible - to study directly in humans. 



Because 2D:4D is also connected to cognitive traits and mental health conditions, this research could help explain sex-based differences in disorders like <a href="https://www.earth.com/news/toddler-screen-time-linked-to-atypical-sensory-behaviors/">autism</a>, <a href="https://www.earth.com/news/how-gut-bacteria-morganella-morganii-could-cause-depression-not-a-brain-disorder/">depression</a>, or attachment issues.



<h2 class="wp-block-heading" id="h-biology-is-not-the-whole-story">Biology is not the whole story</h2>



While the findings are compelling, they also raise important questions. For one, it’s still unclear how well results from rats translate to humans. 



Rats provide a useful model for controlled experiments, but human sexuality is influenced by many layers - cultural, social, psychological - that go far beyond biology.



The researchers also focused only on male rats. Future studies will need to explore whether similar patterns hold true for females, and how other factors like environment or stress interact with digit ratios to shape behavior.



Another key question is causation. Rats with shorter 2D:4D finger ratios tend to show more sexual activity and stronger preferences, but scientists aren’t yet sure whether the digit ratio drives this behavior - or if both stem from shared prenatal influences.



None of this takes away from the value of the study. But it highlights the importance of treating biological markers like 2D:4D as part of a much larger picture. 



The full study was published in the journal <a href="https://www.jstage.jst.go.jp/article/expanim/advpub/0/advpub_24-0159/_article" target="_blank" rel="noreferrer noopener">Experimental Animals</a>.



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Does your finger length predict sexual behavior? A new study says yes

Sexual behavior and preference - whether in humans or animals...

Ants, with their unique genes, outnumber people by roughly 2.5 million to one. Their combined dry mass, about 12 million tons of carbon, rivals one‑fifth of humanity’s weight on land.



An international research team has compared 163 ant genomes to show how these <a href="https://www.earth.com/news/swarm-intelligence-ants-can-anticipate-obstacles-and-plan-ahead/">insects</a> turned cooperative living into an evolutionary engine. They reshuffled DNA while guarding key caste <a href="https://www.pnas.org/doi/10.1073/pnas.2201550119" target="_blank" rel="noreferrer noopener">genes</a> for more than 100 million years.



<h2 class="wp-block-heading" id="h-genetic-clues-to-colony-life">Genetic clues to colony life</h2>



Dr. Lukas Schrader of the <a href="https://www.uni-muenster.de/en/" target="_blank" rel="noreferrer noopener">University of Münster</a> helped coordinate the <a href="https://www.cell.com/cell/fulltext/S0092-8674(25)00617-8" target="_blank" rel="noreferrer noopener">project</a> and still sounds amazed by its scope.



<a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC2665839/" target="_blank" rel="noreferrer noopener">Charles Darwin</a> once fretted over sterile workers, calling them a “special difficulty” because natural selection seemed unable to favor individuals that never breed. 



Inclusive‑fitness theory, formalized in 1964, solved the logic by showing that workers spread their genes by helping sisters.



The new data add genetic proof to that idea: worker‑specific <a href="https://www.earth.com/news/how-many-ants-live-on-earth-at-any-point-in-time-total-number-is-astounding/">gene</a> clusters stayed almost identical across lineages, hinting that any mutation hurting brood care was swiftly purged.



<h2 class="wp-block-heading" id="h-ant-colonies-behave-like-bodies">Ant colonies behave like bodies</h2>



Biologists label an ant colony a superorganism because its members behave like cells of one body. 



The new <a href="https://www.cell.com/cell/fulltext/S0092-8674%2825%2900617-8" target="_blank" rel="noreferrer noopener">dataset</a> spans army ants with millions of workers, species such as Camponotus japonicus whose queens dwarf their tiniest laborers more than 100‑fold, and even parasites that have lost workers altogether.



Researchers sequenced 145 species from 25 countries and folded in 18 earlier genomes to reach chromosome‑level quality for 17 of them. That’s no small feat when many ants are smaller than a comma.



“The publication is a milestone in our understanding of the molecular and genetic foundations of ants and probably also other social <a href="https://www.earth.com/news/how-ants-could-help-stop-the-tree-killing-lanternfly/">insects</a> such as honeybees,” said Schrader.



Across the tree, queen and worker blueprints sit side by side. Yet workers never hatch reproductive organs because development is rerouted by hormones and gene‑regulation circuits embedded in the shared DNA.



<h2 class="wp-block-heading" id="h-ants-keep-critical-survival-genes">Ants keep critical survival genes</h2>



The study tracked <a href="https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/synteny" target="_blank" rel="noreferrer noopener">synteny</a>, the order of genes along a chromosome. Whole blocks had flipped, fused, or fractured at a rate up to four times that seen in vertebrates. Ant groups with the fastest breakage spawned the most species.



Even so, 970 tiny gene clusters, street blocks in the genetic city, remained frozen across 80 percent of species. Many code for metabolism and caste traits, suggesting that breaking them would cripple <a href="https://www.earth.com/news/paleontologists-found-the-oldest-ant-species-on-earth-113-million-years-old-with-scythe-like-jaws/">colony</a> function.



One conserved block houses two <a href="https://www.sciencedirect.com/topics/neuroscience/vitellogenin" target="_blank" rel="noreferrer noopener">vitellogenin genes</a> vital for queen egg yolk and sits unchanged in 148 genomes. Another links fatty‑acid enzymes to worker‑biased expression, underlining how diet and labor intertwine.



Holding those modules steady while the surrounding landscape rearranged let ants explore new lifestyles without losing the caste machinery that keeps colonies alive.



<h2 class="wp-block-heading" id="h-hormones-decide-jobs-and-stability">Hormones decide jobs and stability</h2>



A single molecule can tip a larva toward royalty or toil. <a href="https://www.pnas.org/doi/10.1073/pnas.2406999121" target="_blank" rel="noreferrer noopener">Juvenile hormone</a> has long been that switch, and gene copies for the enzyme <a href="https://www.pnas.org/doi/10.1073/pnas.2134232100" target="_blank" rel="noreferrer noopener">JHAMT</a> rise in species with extreme queen‑worker size gaps.&nbsp;



Insulin and <a href="https://www.science.org/doi/10.1126/science.abm8767" target="_blank" rel="noreferrer noopener">MAPK signaling</a> join the act. In the jumping ant Harpegnathos, blocking MAPK with the drug trametinib makes workers grow larger, echoing lab findings that this pathway expands ovaries when workers become egg‑laying gamergates.&nbsp;



The new comparison shows MAPK genes under intensified selection in lineages where workers can still replace a queen, but relaxed selection where caste roles are rock‑solid. 



That fits the idea that plastic colonies need fine hormonal tuning, while rigid ones lock their switches.



Hormone receptors for juvenile hormone and insulin sit inside conserved synteny islands. This hints that the entire endocrine toolkit rode through deep time as a connected package.



<h2 class="wp-block-heading" id="h-ant-genes-shift-with-colony-size">Ant genes shift with colony size</h2>



Bigger colonies and steeper queen‑worker dimorphism marched together in evolution; both correlate with trails, trophallaxis, and worker polymorphism. 



Genes tied to brain development, such as <a href="https://www.genecards.org/cgi-bin/carddisp.pl?gene=GCM1" target="_blank" rel="noreferrer noopener">GCM</a> and the <a href="https://www.ncbi.nlm.nih.gov/gene/37892" target="_blank" rel="noreferrer noopener">muscarinic receptor mAChR‑A</a>, show worker‑type biased activity and signs of adaptive change in species sporting soldiers beside tiny foragers.



Where workers lost ovaries altogether, selection on oogenesis genes like otu relaxed, but those same genes stay under pressure in species whose workers can still lay male eggs.



Social parasites flip the pattern. Workerless inquilines shed odorant‑receptor genes and rack up chromosomal breaks, mirroring their narrow ecological niche and tiny population sizes.



<h2 class="wp-block-heading" id="h-ant-genes-explain-social-evolution">Ant genes explain social evolution</h2>



Many themes, hormonal control, preserved gene neighborhoods, break‑induced innovation, also shape honeybees, wasps, and higher termites. Ants simply had a 150‑million‑year head start, offering a living time machine for social evolution.



Knowing which genes stay linked during caste splits could aid synthetic‑biology efforts that aim to engineer division of labor in microbes or even tissues.



The study also reminds us that nature can be both flexible and conservative: colonies reinvent chromosome layouts yet keep critical circuits intact, a balance worth emulating in adaptive technologies.



Ants may be tiny, but their genomes read like manuals on how cooperation rewires life. Future research will test whether the same genetic choreography repeats whenever individual interests yield to collective success.



The study is published in the journal <a href="https://www.cell.com/cell/fulltext/S0092-8674(25)00617-8" target="_blank" rel="noreferrer noopener">Cell</a>.



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Ant genes show how evolution created perfect teamwork

Ants, with their unique genes, outnumber people by roughly 2.5...

Milk, a staple in countless diets worldwide, now faces an uncertain future. As climate change accelerates, its effects are being felt far beyond melting glaciers and rising seas. 



One of the most troubling consequences is unfolding silently in dairy farms - where heat is becoming an ever-present threat.



Heat stress in cows is not new. Dairy farmers have long dealt with summer slumps in <a href="https://www.earth.com/news/new-study-shows-that-dairy-milk-cheese-consumption-improves-gut-biodiversity-health/">milk</a> production. But today's climate shifts are not just occasional hurdles. They are becoming regular, intense, and prolonged. 



Scientists now warn that the future of milk production could face irreversible changes, with major impacts on food supplies and farmer livelihoods.



A recent study offers deep insight into this challenge. It reveals that extreme heat reduces milk yields by up to 10 percent, and cooling systems are only partly effective. The results highlight the limits of technology in fighting nature’s heat waves.



<h2 class="wp-block-heading" id="h-extreme-heat-is-cutting-milk-production">Extreme heat is cutting milk production</h2>



The study examined 320 million daily records from Israeli <a href="https://www.earth.com/news/drinking-raw-milk-health-hazard-pasteurization-important/">dairy</a> farms over 12 years. It shows that extreme humid heat reduces milk yield by up to 10 percent. These effects linger beyond 10 days.



“Climate change will have wide-ranging impacts on what we eat and drink, including that cold glass of milk,” said Eyal Frank, an assistant professor at the <a href="https://harris.uchicago.edu" target="_blank" rel="noreferrer noopener">Harris School of Public Policy</a>.



Even farms with the best technology could only offset less than half of these losses.



<h2 class="wp-block-heading" id="h-israeli-farms-offer-global-insights">Israeli farms offer global insights</h2>



Israel's dairy sector uses advanced technology and operates under government-controlled <a href="https://www.earth.com/news/dairy-farms-can-join-the-climate-fight-by-trapping-methane/">milk</a> prices. 



The researchers gathered data from more than 130,000 cows. They also surveyed 306 farmers on their heat mitigation strategies, including cooling technologies.



“The dairy industry in Israel is a good testbed because farms are scattered throughout the country and experience a wide range of temperatures and humidity that represent conditions for top milk producing countries around the world,” noted Ram Fishman, associate professor of Public Policy at <a href="https://english.tau.ac.il" target="_blank" rel="noreferrer noopener">Tel Aviv University</a>.



<h2 class="wp-block-heading" id="h-humid-heat-causes-sharp-milk-declines">Humid heat causes sharp milk declines</h2>



The study shows milk yields fall sharply when wet-bulb temperatures exceed 26°C (78.8°F). Wet-bulb temperature captures both heat and humidity, making it more accurate for gauging heat stress.



When cows face these <a href="https://www.earth.com/news/raw-milk-could-carry-deadly-flu-viruses-for-days/">conditions</a>, production drops by nearly 10 percent. It also takes more than 10 days for milk output to recover.



Cooling systems, such as fans and sprinklers, help but lose effectiveness as temperatures rise.



<h2 class="wp-block-heading" id="h-cooling-helps-but-only-partially">Cooling helps, but only partially</h2>



Cooling equipment can cut losses by about half on moderately hot days. However, on hotter days, this protection weakens.



Farms typically recoup cooling costs within 1.5 years, making it a profitable, though incomplete, solution.



“Dairy farmers are well aware of the negative impacts that heat stress has on their herds, and they use multiple forms of adaptation,” says Ayal Kimhi, associate professor at the <a href="https://en.huji.ac.il" target="_blank" rel="noreferrer noopener">Hebrew University of Jerusalem</a>.



<h2 class="wp-block-heading" id="h-heat-damage-to-milk">Heat damage to milk </h2>



The researchers discovered that heat’s effects on milk production can last longer than previously believed.



Ten consecutive days of humid heat can reduce yields by up to 26 percent. These prolonged impacts suggest that heat stress accumulates, making recovery slow and difficult.



Some farms also shift calving periods and change feeding schedules to reduce heat impacts. These additional tactics offer slight benefits. Farms using both calving and feed adjustments showed better resilience during extreme heat.



Still, the researchers found that these methods offer limited protection compared to the scale of the problem.



<h2 class="wp-block-heading" id="h-future-heat-will-worsen-milk-shortages">Future heat will worsen milk shortages</h2>



The research models future scenarios for major dairy-producing countries. Without cooling, these nations may lose up to 4 percent of their annual milk production by mid-century.



India, Pakistan, and Brazil face some of the largest losses. Cooling can reduce some of the impact, but not eliminate it.



The study also highlights that even with cooling, losses persist in countries like the United States and China.



<h2 class="wp-block-heading" id="h-rethinking-dairy-adaptation">Rethinking dairy adaptation</h2>



The researchers found a clear trade-off. Higher-producing cows suffer more from heat stress.



Milk losses are highest during early lactation stages and among older cows that produce more milk. This trade-off raises concerns about the long-term sustainability of high-output dairy systems.



The study raises questions about current dairy farming practices. Full indoor housing can reduce heat exposure but introduces new problems, like stress from confinement.



“Our research underscores the value and the limitations of cooling technologies and other efforts taken by dairy farmers to adapt to climate change,” said Claire Palandri, a postdoctoral scholar at the Harris School of Public Policy.



Palandri urges policymakers to explore alternative ways to ease heat stress on cows, such as reducing confinement or allowing more natural behaviors, to protect milk production in a warming world.



The study is published in the journal <a href="https://www.science.org/doi/10.1126/sciadv.adw4780" target="_blank" rel="noreferrer noopener">Science Advances</a>.



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Milk prices are rising with the heat around the world due to production issues

Milk, a staple in countless diets worldwide, now faces an...

Phyllium,Is,The,Largest,And,Most,Widespread,Genus,Of,Leaf

In the wild, survival often depends on looks. Some insects evolve disguises that trick their predators into keeping a safe distance. One of the most fascinating examples of this is <a href="https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/batesian-mimicry" target="_blank" rel="noreferrer noopener">Batesian mimicry</a>, where harmless species mimic dangerous ones.



Predators that are wary of painful stings, or toxic bites, learn to avoid the warning patterns on the bodies of these potential prey species. 



But some other species evolve to copy these signals, despite being completely harmless themselves. This strange dance of deception shapes the appearance of many species worldwide.



Recently, researchers at the <a href="https://www.nottingham.ac.uk" target="_blank" rel="noreferrer noopener">University of Nottingham</a> pushed this idea further. They explored how advanced 3D printing technologies can unravel mysteries surrounding mimicry. Their results revealed surprising insights about evolution, <a href="https://www.earth.com/news/insects-are-still-disappearing-and-there-are-hundreds-of-reasons-why/">predators</a>, and survival strategies.



This study not only shines a light on insect mimicry but also offers a deeper look at the forces that mold nature’s endless forms.



<h2 class="wp-block-heading" id="h-how-predators-judge-insect-disguises">How predators judge insect disguises</h2>



The Nottingham team, led by Dr. Tom Reader and Dr. Christopher Taylor, decided to take an experimental leap. They created life-size, 3D-printed models of insects to study how predators respond to different levels of mimicry.



By controlling every aspect of these models - such as shape, color, size, and patterns - they crafted accurate representations of real <a href="https://www.earth.com/news/rising-heat-shrinking-habitats-insects-face-hidden-threats/">species</a>. These included wasps that are known for their stings, and hoverflies that are famous mimics of wasps.



This approach allowed the scientists to explore a central question: Why do some mimics look almost identical to their models, while others resemble them only vaguely?



With 3D printing, they could manipulate every trait precisely and test how predators react to slight variations. This marked a significant step beyond previous studies that relied on natural specimens alone.



“In our study, we are asking a question about how evolution works and what determines where evolution reaches at a particular point in time," Dr. Reader said.



"Our experiments looked at the competing influences which might ultimately shape what organisms look like. Insects and mimicry offer a powerful and accessible way to investigate questions that are relevant across the entire tree of life,” he explained.



<h2 class="wp-block-heading" id="h-color-and-shape-matter">Color and shape matter</h2>



The team employed cutting-edge imaging tools to scan real wasps and <a href="https://www.earth.com/news/hoverflies-navigate-by-aligning-their-bodies-with-the-sun/">hoverflies</a>. Then, using advanced morphing software, they modified these images to create insects with varying degrees of accuracy in terms of mimicry.



These experiments allowed the researchers to demonstrate the potential for using modern 3D imaging, along with computer morphing, to design insect models that displayed many different combinations of colors and patterns, shapes and sizes.



“The models enabled us to ask ‘what-if’ questions about these insects. What if they were better mimics because their color was more wasp-like?" said Dr. Taylor.



"It allowed us to play around with the insect’s appearance in a way you can’t with real specimens," he said. "Which meant we could ask a much broader range of questions about what it is that makes a good or bad mimic.”



This experimental flexibility opened new doors for exploring mimicry. The researchers could fine-tune every trait independently and combine them in unexpected ways.



Their key aim was to understand how much precision a mimic needs in order to avoid being eaten. They also wanted to see why poor mimics still manage to survive in nature.



<h2 class="wp-block-heading" id="h-birds-demand-better-insect-disguises">Birds demand better insect disguises</h2>



In their experiments, the scientists presented their models to real predators in controlled settings. Their main subjects were wild birds, particularly great tits, which rely heavily on sight to identify prey.



The results showed that birds responded strongly to variations in mimicry. They focused mainly on color and size, ignoring finer pattern details.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/insect-imitation_3d-printed-wasps_credit-UNottingham_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/insect-imitation_3d-printed-wasps_credit-UNottingham_1s.webp" alt="3D printed models of a common wasp. The model in front is life-sized. Credit: Dr. Tom Reader (University of Nottingham)" class="wp-image-1976458"/></a><figcaption class="wp-element-caption">3D printed models of a common wasp. The model in front is life-sized. Click image to enlarge. Credit: Dr. Tom Reader (University of Nottingham)</figcaption></figure>



The birds were quick learners. They soon began to avoid models that looked more like wasps, even if those models were still rewarding to eat.



Interestingly, the team discovered that intermediate mimics, those blending traits of two different wasp models, gained no extra protection. Birds seemed to prefer clear signals over mixed ones, demanding accurate mimicry.



<h2 class="wp-block-heading" id="h-sloppy-mimics-still-survive">Sloppy mimics still survive</h2>



While birds proved strict judges, invertebrate predators reacted differently. The team tested crab spiders, jumping spiders, and mantises alongside birds to compare predator responses.



Invertebrates showed less concern about precise mimicry. They tolerated models with poor resemblance and attacked more broadly.



This revealed an important insight: <a href="https://www.earth.com/news/ocean-noise-can-be-fatal-to-marine-invertebrates/">invertebrates</a> impose weaker pressure on mimics to evolve perfect disguises. Some insects can survive despite their sloppy mimicry if their main threats come from these predators.



This creates a fascinating evolutionary tension. Birds push for more accurate mimics, but invertebrates allow greater variation to persist.



<h2 class="wp-block-heading" id="h-how-evolution-shapes-insect-disguises">How evolution shapes insect disguises</h2>



A major breakthrough in this study was the creation of an adaptive <a href="https://www.earth.com/news/modern-farming-is-causing-many-insect-species-to-collapse/">landscape</a> for mimicry. By using their 3D printed models, the team could systematically map how changes in traits affected predator decisions.



They designed smooth transitions between models, allowing them to visualize shifts in predator responses as traits varied. The experiments showed that the landscape was steep for color and size, traits that birds select strongly for, but flatter for other features like pattern.



This landscape explained why some mimics evolve to look highly accurate, while others remain imperfect. It all depends on the types of predators in their environment.



In bird-heavy areas, precise mimicry becomes essential. In areas dominated by invertebrates, imperfect mimics can survive without major risks.



<h2 class="wp-block-heading" id="h-simulating-future-disguises">Simulating future disguises</h2>



3D modeling and visualization tools allow researchers to create life-size, full-color models of potential past or future hoverflies and then test them with real predators like birds and <a href="https://www.earth.com/news/spiders-adapt-their-webs-to-filter-out-human-made-noise/">spiders</a> to see how they respond to those traits.



“As an evolutionary biologist, you are constantly trying to understand something that happened in the past, and without a time machine you can’t know how a hoverfly ended up like it did, " Dr. Reader said.



This study not only revealed the subtle pressures shaping insect disguises today but also hinted at how those forces may have operated throughout history.



By bridging technology and biology, the team has crafted a remarkable tool for studying evolution. Their work helps explain how nature fine-tunes survival strategies and keeps evolving in unexpected ways.



Their experiments brought new clarity to questions that have puzzled scientists for decades, showing how insect mimicry remains one of nature’s most astonishing tricks.



The study is published in the journal <a href="https://www.nature.com/articles/s41586-025-09216-3" target="_blank" rel="noreferrer noopener">Nature</a>.



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Mimicry among insects: 3D models reveal how nature's disguises trick predators

In the wild, survival often depends on looks. Some insects...

Thirty‑five millennia may sound like a long time, yet for a mammal, it is practically yesterday. A new study uses whole‑genome data to show that the Norwegian lemming, Lemmus lemmus, split from its Siberian cousin only about 35,000 years ago.



“The Norwegian lemming is a key ecological species in the Fennoscandian tundra. Among other things, it serves as primary food for many predator <a href="https://www.earth.com/news/arctic-animals-evolved-in-different-ways-to-beat-the-cold/">species</a>, including some threatened ones such as the Arctic fox,” said David Díez del Molino, a researcher at the Centre for Palaeogenetics, <a href="https://www.su.se/">Stockholm University</a>.



<h2 class="wp-block-heading" id="h-lemmings-shape-arctic-life">Lemmings shape Arctic life</h2>



Ecologists have tracked lemming booms and busts for decades because those <a href="https://besjournals.onlinelibrary.wiley.com/doi/10.1046/j.1365-2656.1999.00258.x" target="_blank" rel="noreferrer noopener">cycles</a> ripple through the tundra food web, shaping the breeding success of Arctic foxes, owls, and even geese. 



When rodent numbers crash, fox litters shrink, snowy owls skip nesting, and grasses rebound after seasons of heavy grazing.



Unlike most small <a href="https://www.earth.com/news/world-water-day-2025-preserving-glaciers-protecting-our-future/">mammals</a>, Norwegian lemmings overwinter aboveground by tunneling under snow, a habit that keeps them active when many rodents lie low. Their winter wanderings aerate soil, mix plant nutrients, and feed predators during the hungriest months.



During peak years, the species can reach densities of hundreds per acre. Yet its loud squeaks and bold charge‑and‑bite defense make predators think twice, granting the animal an outsized ecological voice relative to its three‑ounce frame.



<h2 class="wp-block-heading" id="h-lemmings-became-a-separate-species">Lemmings became a separate species</h2>



Researchers compared nine modern and two ancient lemming genomes and found a clean split from the Western Siberian lemming with no evidence of crossbreeding, even in areas where the two meet today. 



That result stands in sharp contrast to polar bears and brown bears, whose DNA still shows <a href="https://pubmed.ncbi.nlm.nih.gov/22517859/" target="_blank" rel="noreferrer noopener">ancient admixture</a> from repeated hybridization events.



“Our findings indicate that the Norwegian lemming is among the most recently evolved <a href="https://www.earth.com/news/world-otter-day-2025-on-the-front-lines-of-a-habitat-crisis/">mammals</a>, diverging from its sister taxon, the Western Siberian lemming, at a remarkably shallow time depth,” said <a href="https://palaeogenetics.com/people/edana-lord/" target="_blank" rel="noreferrer noopener">Edana Lord</a>, a postdoctoral researcher at the Centre for Palaeogenetics.



The team’s high‑resolution sequencing also resolved relationships within the genus Lemmus, confirming that Eastern Siberian lemmings belong to a separate species and helping clean up a century of contested rodent taxonomy.



<h2 class="wp-block-heading" id="h-a-species-born-in-an-ice-age">A species born in an ice age</h2>



The divergence date places the split just before the <a href="https://www.science.org/doi/10.1126/science.1172873" target="_blank" rel="noreferrer noopener">Last Glacial Maximum</a>, when ice sheets peaked between roughly 26,500 and 19,000 years ago. 



Glacial barriers likely trapped an ancestral lemming population in a Scandinavian refuge, cutting gene flow with Siberian relatives and setting the stage for rapid speciation.



Once the ice retreated, the newly minted Norwegian lineage expanded westward, but climatic swings had already written separation into the animals’ DNA. Modern population genetics shows no trace of later contact, suggesting that geography and behavior together kept the young species distinct.



Because the entire living population coalesces to a common ancestor only about 6,400 years ago, every Norwegian lemming alive today shares surprisingly shallow roots, a reminder that dramatic evolutionary change can happen fast.



<h2 class="wp-block-heading" id="h-color-blocks-crossbreeding">Color blocks crossbreeding</h2>



Hybridization often lingers for thousands of years after a split, yet these rodents seem to have slammed the door shut. 



One reason may be their vivid black‑and‑yellow coat, a pattern that functions as an <a href="https://www.amnh.org/explore/news-blogs/aposematism-warning-signals" target="_blank" rel="noreferrer noopener">aposematic warning</a> and an instant badge of identity, reducing mating mistakes with the drab Siberian form.



Aggressive ritual boxing, loud chirps, and high‑speed chases further isolate the species by favoring individuals that court their own kind and bully outsiders away from snow burrows.



<h2 class="wp-block-heading" id="h-genes-that-power-survival">Genes that power survival</h2>



Sequencing uncovered unique changes in the <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3093193/" target="_blank" rel="noreferrer noopener">LYST pigment gene</a> that help produce the lemming’s splashy jacket, a mutation class also linked to altered melanosome function in laboratory mice. 



The same region shows signs of a recent selective sweep, hinting at strong predator‑driven pressure for conspicuous colors.



Other <a href="https://pubmed.ncbi.nlm.nih.gov/30006135/" target="_blank" rel="noreferrer noopener">mutations</a> appear in <a href="https://www.ncbi.nlm.nih.gov/gene/53630" target="_blank" rel="noreferrer noopener">BCO1</a>, <a href="https://medlineplus.gov/genetics/gene/apob/" target="_blank" rel="noreferrer noopener">APOB</a>, and <a href="https://www.genecards.org/cgi-bin/carddisp.pl?gene=RELCH" target="_blank" rel="noreferrer noopener">RELCH</a> - genes involved in fat transport and storage; in mice, knocking out BCO1 triggers fatty‑liver disease and shifts cholesterol pathways. Extra‑efficient lipid metabolism may keep lemmings fueled through subzero winters when seeds are scarce.



The researchers also found clusters of rapidly evolving olfactory receptor genes, suggesting that a refined sense of smell guides the rodents through deep snow tunnels to mates, food, and lurking stoats.



<h2 class="wp-block-heading" id="h-lessons-for-arctic-mammals">Lessons for Arctic mammals</h2>



Climate upheaval can spin off new <a href="https://www.earth.com/news/aquatic-robot-inspired-by-flatworms-can-swim-in-harmony-with-nature/">species</a> in a geological blink, and the lemming’s youth underscores how quickly isolation plus selection can rewrite a mammal’s genetic blueprint. 



Similar patterns play out in Arctic whales, foxes, and hares as shrinking ice opens and closes migration corridors.



“This work represents a big step in our understanding of lemming speciation and evolution,” said Love Dalén, a professor in <a href="https://utbildning.su.se/english/education/course-catalogue/bl/bl7082" target="_blank" rel="noreferrer noopener">Evolutionary Genomics at Stockholm University</a>. 



Professor Dalén noted that tracing ancient DNA in more Pleistocene specimens could reveal exactly when each adaptive mutation took hold.



The study is published in <a href="https://www.pnas.org/doi/10.1073/pnas.2424333122" target="_blank" rel="noreferrer noopener">Proceedings of the National Academy of Sciences</a>.



 n

How Norwegian lemmings rapidly evolved into a new species

Thirty‑five millennia may sound like a long time, yet for...

Poke around a British rockpool and you may spot a shell shuffling over the sand. Inside is a hermit crab - an animal that spends much of its life testing the outside world before deciding whether it is safe to venture forth.



New research from the <a href="https://www.plymouth.ac.uk/">University of Plymouth</a> reveals that the speed of that decision, a trait biologists call boldness, hinges on a crab’s built-in sensory toolkit.



The study focuses on microscopic hair-like structures called sensilla that pepper the claws of Pagurus bernhardus, a common UK species.



By counting those hairs on dozens of individuals and matching the totals to behavior in the lab, the team discovered a clear pattern: more sensilla equals faster recovery from a startle response. 



Hermit crabs so equipped are not only bolder, they are also more predictable - showing similar, rapid emergence times across repeated tests.



<h2 class="wp-block-heading" id="h-measuring-crab-response-times">Measuring crab response times</h2>



The experiment began with a simple but telling ritual. Researchers placed each crab in a small tank and gently startled it with a puff of water or a light tap on the shell.



That cue mimics the sudden pressure wave generated by a <a href="https://www.earth.com/news/climate-chaos-caused-a-mass-extinction-of-top-marine-predators/">predator</a> or rolling wave, prompting the animal to yank its legs and antennae inside its borrowed shell. The team then timed how long it took for eye stalks and claws to reappear.



About a third of a second is considered lightning fast in hermit-crab terms; several minutes, positively timid. Over repeated trials, certain individuals consistently clocked shorter hideouts, indicating a stable personality trait rather than random chance.



“I was especially intrigued by how they used their claws and other sensory appendages, such as their antennae, in their explorations and when re-emerging from their shell,” said lead author Ari Drummond, a PhD student at the University of Plymouth.



That curiosity led to the hunch that claws might act as information-gathering probes, letting crabs “sniff” the water for chemical cues or feel subtle <a href="https://www.earth.com/news/small-ocean-currents-play-a-huge-role-in-earths-climate/">currents</a> that betray lurking threats.



<h2 class="wp-block-heading" id="h-claw-molts-reveal-sensors">Claw molts reveal sensors</h2>



Linking behavior to anatomy required patience. Hermit crabs, like all crustaceans, periodically molt. During this process, they shed the outer exoskeleton, including the thin cuticle covering each sensillum.



Drummond and colleagues waited for each test subject to <a href="https://www.earth.com/news/cambrian-fossils-reveal-new-clues-about-arthropod-evolution/">molt</a> naturally, collected the discarded claw tissue, and examined it under a scanning electron microscope.



The high-resolution images looked like alien landscapes - ridged terrain studded with evenly spaced bristles. Each bristle is a sensillum, connected to nerve cells that detect touch, water movement, or dissolved chemicals.



By tracing and counting every sensillum in the images, the team created a detailed sensory map for each crab. This noninvasive method marked a major advance over earlier studies, which often required removing limbs.



Analysis revealed striking variation: some claws sported 50 percent more sensilla than others of similar size. When the researchers plotted those numbers against startle data, the trend became unmistakable. Bolder hermit crabs have more sensilla on the claw surface.



<h2 class="wp-block-heading" id="h-bolder-crabs-have-more-hairs">Bolder crabs have more hairs</h2>



Why would extra sensory hairs translate into courage? The authors propose that better input reduces uncertainty. With richer information about water chemistry or microcurrents, a crab can judge threats more accurately and resume foraging sooner. 



That efficiency, in turn, may feed back into survival and reproductive success, favoring individuals who “invest” in sensory hardware.



They call the concept the “sensory investment syndrome.” It’s a hypothesis linking an animal’s personality - here, boldness - to the resources it allocates to senses. If confirmed across other species, it could reshape how biologists think about behavioral diversity in nature.



“We’ve known for a long time that individual animals of the same species can show consistent behavioral differences from one another,” said senior author Mark Briffa, a professor at Plymouth. 



“Our new research suggests that in hermit crabs, some of this variation may be linked to how individuals sense the world around them.”



In his opinion, similar mechanisms might operate in <a href="https://www.earth.com/news/insects-are-still-disappearing-and-there-are-hundreds-of-reasons-why/">insects</a>, fish, or even mammals, where variation in eye size, whisker density, or olfactory receptors could underpin consistent behavioral tendencies.



<h2 class="wp-block-heading" id="h-crab-survival-starts-with-sensing">Crab survival starts with sensing</h2>



Hermit crabs face mounting challenges: coastal pollution, <a href="https://www.earth.com/news/rising-temperatures-will-cut-world-gdp-by-a-staggering-40-percent-if-nothing-changes/">rising temperatures</a>, and habitat disturbance all alter the sensory landscape of rockpools. Understanding how these creatures sense and decide may reveal which populations are most at risk from environmental change.



“In a world where environments and species are increasingly at risk from human impacts, it is essential that we gain a better understanding of what information animals detect, how they use that information and then respond to stay alive,” Drummond said.



Future work will test what each sensillum detects and whether diet, growth, or shell choice affects hair abundance. 



For now, the takeaway is clear: in the miniature dramas playing out between tide and shore, knowledge is power - delivered through a forest of microscopic hairs on a tiny claw.



The study is published in the journal <a href="https://royalsocietypublishing.org/doi/10.1098/rspb.2025.0932">Proceedings of the Royal Society B</a>.



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Microscopic hairs drive courage in hermit crabs

Poke around a British rockpool and you may spot a...

Sagging beams and hollow‑sounding walls can signal a menace that quietly drains bank accounts around the world - termites. Building owners and insurers spend close to $5 billion a year fixing damage and fighting infestations.



Now, a team of researchers led by <a href="https://profiles.ucr.edu/app/home/profile/dchoe003" target="_blank" rel="noreferrer noopener">Dong‑Hwan Choe</a> at the University of California, Riverside (<a href="https://www.ucr.edu/" target="_blank" rel="noreferrer noopener">UCR</a>) say they can coax the culprits to a pinpoint dose of insecticide by copying the smell of their favorite meal. 



<h2 class="wp-block-heading" id="h-how-termites-cause-problems">How termites cause problems</h2>



The western drywood termite, <a href="https://edis.ifas.ufl.edu/publication/IN526" target="_blank" rel="noreferrer noopener">Incisitermes minor</a>, thrives along the Pacific Coast and has hitchhiked as far as Florida, Georgia, and even Ontario. 



Its colonies live entirely inside dry wood, so they can chew unseen for years before a blistered board betrays them.



Beyond structural headaches, the insects <a href="https://www.earth.com/news/termites-are-natures-architects-building-well-ventilated-nests/">recycle fallen trees</a> in forests, yet in houses the same appetite leaves rafters brittle and doorframes warped. 



Because they need no soil contact, second‑story condominiums and attic beams are just as vulnerable as ground‑floor studs.



Field surveys show overlapping termite <a href="https://www.earth.com/news/termites-play-an-unexpected-role-in-rainforest-revival/">colonies are common</a> in older buildings, compounding the pace of destruction. Inspectors have documented boards reduced to paper‑thin shells while the painted exterior looked intact.



When swarming season peaks, thousands of alates emerge through ventilation gaps, searching for new lumber to colonize. A single missed pair can restart the cycle inside a freshly repaired wall.



<h2 class="wp-block-heading" id="h-why-fumigation-falls-short">Why fumigation falls short</h2>



The go‑to remedy, whole‑structure tenting, bathes a building in the <a href="https://www.nature.com/articles/s43247-024-01294-x" target="_blank" rel="noreferrer noopener">gas sulfuryl fluoride</a>, a pesticide that lingers in the atmosphere for roughly forty years and traps heat far more effectively than carbon dioxide.



Homeowners must vacate for several days, double‑bag food, and trust that every gallery fills with gas, yet the treatment leaves no residue to deter the next swarm.



California alone releases up to <a href="https://insideclimatenews.org/news/03042024/california-sulfuryl-fluoride-emissions/" target="_blank" rel="noreferrer noopener">85 percent</a> of U.S. sulfuryl fluoride emissions, underscoring the climate cost of repeat tentings. 



Each fresh infestation starts the clock, forcing many coastal residents to pay for fumigation every three to five years.



<h2 class="wp-block-heading" id="h-a-scent-straight-from-the-forest">A scent straight from the forest</h2>



<a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC8222632/" target="_blank" rel="noreferrer noopener">Pinene</a> is the crisp aroma wafting from pine needles and conifer sap. For termites the smell signals digestible cellulose rather than festive wreaths.



“Even at low concentrations, pinene is good at attracting termites from a distance,” said Choe. 



Her team reasoned that drifting molecules could guide workers through their winding tunnels toward a precisely drilled injection point. 



Even at parts‑per‑billion levels, the compound spreads faster in air pockets than liquid insecticide can seep through wood fibers.



<h2 class="wp-block-heading" id="h-testing-on-termites-in-the-lab">Testing on termites in the lab</h2>



The experiments, paired a fipronil plug with an identical plug laced with pinene to mimic local injections in framing lumber. 



Termites released into artificial galleries quickly left their <a href="https://www.earth.com/news/hybrid-termites-could-spread-worldwide-from-florida-boats/">aggregation sites</a> and contacted the treated zone.



“Without pinene, we got about 70 percent mortality. When we added it in, it was over 95 percent,” said Choe. 



Video tracking showed most workers reached the scented plug within six hours, and all feeding halted long before visible signs of distress appeared.



<h2 class="wp-block-heading" id="h-what-homeowners-can-expect">What homeowners can expect</h2>



Because the method relies on localized injection, technicians need only a few dime‑size holes instead of circus‑style tarps and warning placards. 



Treated wood stays guarded for years because tiny doses of insecticide remain locked inside the lumber.



The active ingredient, <a href="https://pubmed.ncbi.nlm.nih.gov/23980838/" target="_blank" rel="noreferrer noopener">fipronil</a>, can harm aquatic invertebrates at concentrations below 7 micrograms per liter. 



Embedding the chemical in structural beams slashes the chance of runoff or drift, giving the protocol an environmental edge over perimeter sprays and <a href="https://www.earth.com/news/enormous-desert-structure-termite-mound-built-by-insects-can-be-seen-from-space/">soil drenches</a>.



Early budget modeling by the research group suggests the scent‑boosted injection could cut treatment expenses by half compared with a typical fumigation, since there is no hotel stay, tent rental, or food disposal. 



Contractors also gain scheduling flexibility because residents do not need to vacate, and weather delays become less critical when tarps are no longer part of the plan.



<h2 class="wp-block-heading" id="h-looking-ahead-for-safer-pest-control">Looking ahead for safer pest control</h2>



Choe’s laboratory is cataloging other tree volatiles to see whether <a href="https://www.earth.com/news/enormous-desert-structure-termite-mound-built-by-insects-can-be-seen-from-space/">termite</a> preferences shift with geography or seasonal wood chemistry. 



Matching the lure cocktail to local diets could push effectiveness even higher without raising insecticide doses.



Collaborators in Florida and Japan are testing the approach against Formosan and powderpost drywood relatives, signaling a future where pest management leans on insect noses more than broad‑spectrum gases.



If regulators approve the formulation, builders may someday treat critical beams during construction, turning the lumber itself into a long‑term shield that keeps houses solid and the climate a little cleaner.



The study is published in the <a href="https://academic.oup.com/jee/article-abstract/117/4/1628/7675403?redirectedFrom=fulltext&amp;login=false" target="_blank" rel="noreferrer noopener">Journal of Economic Entomology</a>.



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New system attracts and eliminates termites with a natural scent and no toxins

Sagging beams and hollow‑sounding walls can signal a menace that...

Vanilla is more than just a kitchen staple. It is the world’s most popular spice after saffron and finds its way into everything from ice creams to perfumes and medicines. 



The allure of vanilla's rich, sweet aroma has made it a global commodity, supporting industries and smallholder farmers alike. Yet, hidden behind its widespread appeal lies a fragile reality deeply linked to climate change.



The commercial vanilla crop, derived from the Vanilla planifolia orchid, faces growing challenges. These include threats from drought, heat, and diseases, all of which are worsening under climate change. 



Vanilla <a href="https://www.earth.com/news/traditional-forest-farming-is-an-overlooked-climate-solution/">farming</a> already depends heavily on labor-intensive hand pollination. Any further strain on the species could threaten not only its cultivation but also the livelihoods of many farming communities.



Wild Vanilla species, scattered across the tropics, may hold the key to preserving this treasured crop. They offer a wealth of genetic diversity that could help strengthen cultivated varieties. However, these wild species now face their own climate-driven crises.



<h2 class="wp-block-heading" id="h-how-climate-affects-vanilla-and-pollinators">How climate affects vanilla and pollinators</h2>



Scientists have long recognized the importance of wild Vanilla <a href="https://www.earth.com/news/feeding-the-world-without-harming-nature-the-complex-balance-of-farming/">species</a> as genetic resources. These species possess traits that could improve drought resistance, heat tolerance, and disease resilience in commercial vanilla. However, their survival is tightly linked to pollinators, mainly bees from the Euglossini tribe.



In the natural world, most Vanilla species depend on animal pollinators for reproduction. These intricate relationships, often involving specialized behaviors and physical compatibility, are highly vulnerable to ecological disruptions.



“Climate change may lead to a reduced habitat overlap between Vanilla orchid species and their pollinators, resulting in plant-pollinator decoupling that negatively affects the survival of wild vanilla populations,” said Dr Charlotte Watteyn, a researcher at KU Leuven and the <a href="https://www.ucr.ac.cr" target="_blank" rel="noreferrer noopener">University of Costa Rica</a>.



<h2 class="wp-block-heading" id="h-habitat-shifts-under-climate-pressure">Habitat shifts under climate pressure</h2>



Dr. Watteyn's team analyzed the habitats of 11 Vanilla species along with seven pollinator species. They examined two future climate scenarios: SSP2.4-5 and SSP3-7.0.



The SSP2.4-5 scenario presents moderate climate <a href="https://www.earth.com/news/eco-friendly-farms-can-succeed-but-they-need-support/">risks</a>, with some progress in climate action. In contrast, SSP3-7.0 signals severe challenges, marked by heavy fossil fuel use and limited global cooperation.



Under both scenarios, some Vanilla species may expand their habitats by as much as 140%. However, other species may lose up to 53% of their suitable habitat.



Pollinators face even greater risks. Their suitable habitats are expected to shrink significantly, with the steepest declines under SSP3-7.0. This sharp drop in pollinator populations threatens the entire pollination process.



“Despite the possible increase in suitable habitat for some Vanilla species, their pollinator-dependency may imperil the survival of natural populations,” said Watteyn.



<h2 class="wp-block-heading" id="h-climate-risks-to-vanilla-pollination">Climate risks to vanilla pollination</h2>



Many Vanilla <a href="https://www.earth.com/news/farming-for-wildlife-how-traditional-practices-can-protect-nature/">species</a> rely on distinct pollination methods. Some provide nectar to attract pollinators, while others use deception. Vanilla pompona employs a combination of floral scents and food mimicry to lure bees.



Pollinators, particularly Euglossini bees, face mounting climate threats. Their habitats are expected to shrink, with smaller bee species showing greater vulnerability than larger ones.



“Vanilla species are known for their specialized relationships with pollinators, hence, they may experience difficulties in replacing pollinators,” explained Watteyn. 



Species like V. planifolia and V. trigonocarpa already have limited overlap with their pollinators. Climate change may worsen this.



<h2 class="wp-block-heading" id="h-conservation-priorities-for-vanilla-survival">Conservation priorities for vanilla survival</h2>



The study identified current and future areas where Vanilla <a href="https://www.earth.com/news/climate-change-will-devastate-global-food-production/">species</a> and pollinators overlap. They also flagged areas needing conservation or assisted migration.



By 2050, protected areas covering Vanilla-pollinator overlap could shrink significantly. For example, protected overlap for V. pompona may fall from 42 to 17 percent.



The researchers highlighted areas for urgent conservation. They suggested combining in situ protection with ex situ measures such as seed banks and botanical gardens.



<h2 class="wp-block-heading" id="h-other-threats-beyond-climate">Other threats beyond climate</h2>



Habitat destruction, illegal harvesting, and ecological disruptions also affect Vanilla survival. Many Vanilla species have specific needs, including partnerships with fungi and animals for seed dispersal and germination.



The researchers emphasized the need for more studies on these relationships. “Collaborative research on the ecology and genetic diversity of wild vanilla across its natural distribution is paramount if we want to take vanilla breeding into the future,” said Professor Adam Karremans.



<h2 class="wp-block-heading" id="h-global-vanilla-trade-needs-protection">Global vanilla trade needs protection</h2>



Vanilla remains a major cash crop with high global demand. It supports smallholder farmers worldwide.



“Like cacao and coffee, vanilla is a global export crop with high international market value. It’s grown to make profit, and is a key driver for rural development, agricultural innovation, and overall welfare,” concluded Dr. Watteyn.



Conserving wild Vanilla species now appears essential not just for ecosystems, but also for global food systems. Protecting these species can help secure vanilla’s future amid climate change.



The study is published in the journal <a href="https://www.frontiersin.org/journals/plant-science/articles/10.3389/fpls.2025.1585540/full" target="_blank" rel="noreferrer noopener">Frontiers in Plant Science</a>.



Image Credit: Charlotte Watteyn



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Climate change is separating wild vanilla from its pollinators

Vanilla is more than just a kitchen staple. It is...

Shower water carries more than suds. Every shampoo rinse sends long‑chain chemicals from our bathrooms into rivers where they can cling to the bodies of small aquatic animals.



A research team led by Hans Sanderson of <a href="http://Aarhus University https://g.co/kgs/wGFv7P9">Aarhus University</a> tracked what those ingredients do once they leave the drain, focusing on a class called <a href="https://www.sciencedirect.com/science/article/abs/pii/S0166445X24003485?via%3Dihub" target="_blank" rel="noreferrer noopener">polyquaternium conditioners</a> that make hair feel smooth.



<h2 class="wp-block-heading" id="h-how-shampoos-tame-frizz">How shampoos tame frizz</h2>



Hair carries a natural negative charge, and damaged strands hold even more. Manufacturers add <a href="https://www.sciencedirect.com/science/article/abs/pii/S0166248108701168" target="_blank" rel="noreferrer noopener">positively charged polymers</a> so those long molecules wrap around each fiber and neutralize static, leaving a sleek finish.



The most common sub‑group, polyquaterniums, numbers more than 25,000 variations. Together they support a <a href="https://www.businessresearchinsights.com/market-reports/polyquaternium-market-107659" target="_blank" rel="noreferrer noopener">market valued</a> at about $0.12 billion in 2024 and projected to grow steadily over the next decade.



Each molecule is huge by <a href="https://www.earth.com/news/how-ocean-animals-connect-countries-and-continents/">chemical</a> standards, so toxicology screens once assumed they were harmless to wildlife because they cannot slip through cell membranes. Sanderson’s team asked whether sticking on the outside of a creature could matter just as much.



<h2 class="wp-block-heading" id="h-shampoo-harms-tiny-aquatic-animals">Shampoo harms tiny aquatic animals </h2>



Freshwater ponds and lakes are full of <a href="https://www.ncbi.nlm.nih.gov/books/NBK2042/" target="_blank" rel="noreferrer noopener">daphnia</a>, tiny crustaceans <a href="https://www.earth.com/wp-content/uploads/2025/07/Shampoo-animals.jpg">sometimes called water fleas</a>. They filter algae and bacteria, purify water, and form a primary food source for many small fish.



Because daphnia propel themselves with rhythmic strokes of their antennae, any extra drag can slow them down. 



The Aarhus experiments showed that a film of conditioner polymers glued to the animals’ shells, halving their swimming speed and hindering feeding.



“We have conducted the first study in the world to investigate this. The substances do not penetrate the animals’ cells, but rather stick to the surface of the <a href="https://www.earth.com/news/world-environment-day-2025-plastic-pollution-is-choking-our-planet/">animal</a>,” explained Sanderson. 



“This physically affects the animal, making it unable to move as well, and it impairs its ability to ingest food,” continued Sanderson.



<h2 class="wp-block-heading" id="h-shampoo-s-charge-makes-animals-vulnerable">Shampoo's charge makes animals vulnerable</h2>



The researchers ran complementary tests on two standard laboratory species, <a href="https://www.ncbi.nlm.nih.gov/books/NBK2042/" target="_blank" rel="noreferrer noopener">Daphnia magna</a> and <a href="https://www.inaturalist.org/taxa/483833-Ceriodaphnia-dubia" target="_blank" rel="noreferrer noopener">Ceriodaphnia dubia</a>, using three <a href="https://www.sciencedirect.com/science/article/pii/S0166445X24003485" target="_blank" rel="noreferrer noopener">polyquaterniums</a> of different designs. 



The team found toxicity thresholds as low as 0.05 mg per liter for the most highly charged polymer, while the same molecule with a lower charge was 400‑fold less toxic.



The pattern was consistent regardless of molecular weight. That result shifts regulatory focus from size to <a href="https://www.sciencedirect.com/topics/chemistry/charge-density" target="_blank" rel="noreferrer noopener">charge density</a>, a parameter rarely documented on shampoo labels.



Organic matter in natural water, such as dissolved humic acids, partially blunts the polymers’ stickiness. Yet even moderate concentrations still impaired reproduction and growth during 21‑day chronic tests with both daphnia species.



<h2 class="wp-block-heading" id="h-how-shampoo-chemicals-move-to-animals">How shampoo chemicals move to animals</h2>



Wastewater plants intentionally add the same <a href="https://pubs.acs.org/doi/10.1021/acs.macromol.3c01223" target="_blank" rel="noreferrer noopener">cationic polymers</a> as a <a href="https://www.sciencedirect.com/topics/chemistry/flocculant" target="_blank" rel="noreferrer noopener">flocculant</a> to clump particles together for easier removal. Ironically, what helps strip other pollutants out of sewage can persist in the resulting sludge or treated effluent.



If facilities discharge more than the <a href="https://www.earth.com/news/climate-change-is-impacting-marine-life-more-than-we-realized/">ecosystem</a> can buffer, sensitive invertebrates pay the price. Because daphnia sit near the base of the food web, their decline can ripple upward and reduce fish recruitment.



Laboratory work measured polymer levels that killed half a daphnia population within 48 hours at phone‑screen brightness‑level concentrations. Field monitoring remains limited, so nobody knows how often small streams approach those doses.



<h2 class="wp-block-heading" id="h-call-for-smarter-safety-tests">Call for smarter safety tests</h2>



European agencies already demand hazard labels for chemicals that penetrate cells, but large polymers still slip through many guidelines. 



The European Commission is reviewing <a href="https://single-market-economy.ec.europa.eu/sectors/chemicals/chemicals-legislation_en" target="_blank" rel="noreferrer noopener">polymer assessment rules</a> under its CLP and <a href="https://environment.ec.europa.eu/topics/chemicals/reach-regulation_en" target="_blank" rel="noreferrer noopener">REACH regulations</a>, with updates expected this year.



The researchers argue that future protocols must mimic real‑world water containing organic carbon, rather than the ultra‑clean test media used today. 



They also recommend including movement and feeding endpoints, not just mortality, when assessing ecological risk.



Softening agents may never fully disappear from consumer goods. However, incremental tweaks, lower charge density, biodegradable side chains, or safer alternatives like amino‑based conditioners could cut harm dramatically. 



Manufacturers have incentives to act before formal limits arrive, because production lines adapt faster than legislation.



<h2 class="wp-block-heading" id="h-reducing-shampoo-s-harm-to-animals">Reducing shampoo’s harm to animals</h2>



Reading an ingredient list will often reveal polyquaterniums by number, for example polyquaternium‑10 or ‑7. Lower single‑digit numbers usually carry higher charge density, although the label alone cannot quantify risk.



Choosing rinse‑off products certified for low aquatic toxicity is one stopgap, though Sanderson notes that even ecolabel formulations sometimes rely on the same chemistry. 



Reducing dosage helps too; a quarter‑sized blob of shampoo cleans most medium‑length hair, and conditioner is unnecessary every wash for many people.



Small behavior shifts add up because each bottle skipped prevents thousands of gallons of rinse water from picking up extra polymers over its retail life. 



Until wastewater infrastructure and regulations catch up, prevention at the source remains the surest shield for freshwater communities.



<h2 class="wp-block-heading" id="h-toward-a-balanced-bathroom-shelf">Toward a balanced bathroom shelf</h2>



The story of sticky hair conditioners underscores a broader lesson in polymer safety. Size alone cannot protect wildlife if surface charge lets molecules hijack essential behaviors like swimming and feeding. 



Daphnia, though invisible from a shower stall, signal the health of entire lakes and streams. When their numbers fall, algae blooms can surge, water clarity drops, and fish lose a key snack.



Scientists now have lab tools to screen thousands of conditioning agents quickly, ranking them by how strongly they glue onto living surfaces. 



Policy makers can use that knowledge to set practical discharge limits, while industry chemists re‑engineer formulas for performance without collateral damage.



Every shampoo rinse cycle connects personal routine to planetary processes, affecting animals too. Balancing clean hair with clean water and protecting animals is no longer guesswork; the data are in view, and the solutions are within reach.



The study is published in the journal <a href="https://www.sciencedirect.com/science/article/pii/S0166445X24003485" target="_blank" rel="noreferrer noopener">Aquatic Toxicology</a>.



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Chemicals in shampoos and soaps are infiltrating rivers and killing aquatic life

Shower water carries more than suds. Every shampoo rinse sends...

Far below the ocean’s surface, the Great Barrier Reef hums with life. It is not just about colorful fish or vibrant corals. Something else is happening that we cannot see.



Tiny <a href="https://www.earth.com/news/world-reef-awareness-day-2025-bringing-corals-back-to-life/">coral</a> larvae drift in the currents, carried away from their parents. Some travel far and some barely move at all. Where these larvae end up can decide the fate of entire reefs.



Now, scientists from the <a href="https://www.uq.edu.au" target="_blank" rel="noreferrer noopener">University of Queensland</a> have unlocked a key mystery. Their new study shows how far these baby corals can go. The research also reveals why this matters more than we ever realized.



<h2 class="wp-block-heading" id="h-why-some-coral-babies-survive">Why some coral babies survive</h2>



<a href="https://www.earth.com/news/wild-temperature-swings-boost-coral-reef-resilience/">Corals</a> are under pressure. Heatwaves damage them. Storms cause destruction. Oceans keep getting more acidic. Each year, the risk becomes worse. But not all corals are affected equally. PhD candidate Zoe Meziere explained why some reefs survive better than others.



“Quantifying genetic connectivity can predict the fate of populations as more isolated reefs with lower levels of genetic variation are likely more vulnerable,” said Meziere.



When coral species spread their larvae far, they swap genetic material with distant reefs. This boosts their ability to adapt and recover. Corals that keep their offspring close face greater risks. They may struggle to bounce back after disasters.



<h2 class="wp-block-heading" id="h-coral-species-take-different-paths">Coral species take different paths</h2>



Meziere and her team searched for answers. They focused on two coral species found across the Great Barrier Reef, Stylophora pistillata and Pocillopora verrucosa.



The <a href="https://www.earth.com/news/fossils-reveal-how-humans-completely-changed-caribbean-reef-ecosystems/">species</a> live near each other, but their ways of reproducing could not be more different. Stylophora pistillata plays it safe. It fertilizes its eggs internally. Its larvae do not venture far. Most settle nearby, just meters from their parent colony.



Pocillopora verrucosa does the opposite. It releases eggs and sperm into the sea. Currents carry its larvae far from home.



The results surprised the researchers. Stylophora pistillata larvae traveled only 23 to 102 meters. Pocillopora verrucosa larvae journeyed as far as 52 kilometers.



Professor Cynthia Riginos noted that this is the first study to quantify how connected different coral populations are across the seascape.



<h2 class="wp-block-heading" id="h-why-the-journey-of-baby-corals-matters">Why the journey of baby corals matters</h2>



The story does not stop with distance. These differences shape the future of coral populations.



Stylophora pistillata stays close to home. It forms small, tight populations. Over time, these groups grow isolated. They lose genetic diversity. That leaves them vulnerable. Pocillopora verrucosa travels widely. It links distant populations. This mixing keeps its populations strong and diverse.



“Over time, these differences have profound evolutionary impacts with S. pistillata populations being more genetically distinctive with much lower genetic diversity and smaller population sizes than the more widely dispersing P. verrucosa,” explained Professor Riginos.



<h2 class="wp-block-heading" id="h-where-baby-corals-travel">Where baby corals travel</h2>



The research team did not stop after measuring dispersal. They looked deeper into the genetic maps.



Stylophora pistillata stayed loyal to its local area. Its genetic patterns showed clear boundaries between reefs. Neighboring reefs looked genetically distinct. 



Pocillopora verrucosa showed no such boundaries. Its populations mixed freely throughout the reef. From one end to another, its genetics stayed consistent.



S. pistillata’s world spanned just a few hundred meters, while P. verrucosa’s world stretched across tens of kilometers.



<h2 class="wp-block-heading" id="h-coral-survival-and-recovery">Coral survival and recovery</h2>



Distance is only part of the story. Gene flow also plays a big role. S. pistillata had weak gene flow. Its reefs relied mostly on themselves. This isolation put them at risk. One disaster could wipe out an entire population with no outside help.



P. verrucosa showed strong gene flow, as distant reefs shared genes often. This flow allowed for faster recovery after disasters.



This means that Pocillopora verrucosa can bounce back after bleaching far more quickly than Stylophora pistillata.



<h2 class="wp-block-heading" id="h-some-coral-babies-stay-stronger">Some coral babies stay stronger</h2>



Genetic diversity matters for survival. The researchers found striking differences here too.



Stylophora pistillata had low genetic <a href="https://www.earth.com/news/ancient-coral-collapse-may-help-save-the-great-barrier-reef/">diversity</a>. Its diversity also varied wildly between reefs. The lowest levels appeared in southern parts of the Great Barrier Reef.



Pocillopora verrucosa held onto high diversity. Its genetic richness stayed stable across all reefs. S. pistillata lives in a fragile world, and P. verrucosa thrives in a far more connected one.



<h2 class="wp-block-heading" id="h-smarter-conservation-for-corals">Smarter conservation for corals</h2>



The research offers a clear message for coral conservation efforts. Stylophora pistillata needs focused, local protection. Efforts must center on preserving nearby populations. Without these, this species faces collapse.



Pocillopora verrucosa calls for a broader approach. Large-scale conservation networks can help maintain its natural strength.



"Dispersal and connectivity are important drivers of coral adaptation, and being able to adapt is key to having healthy coral reefs in the future,” said Meziere.



<h2 class="wp-block-heading" id="h-new-approach-to-reef-restoration">New approach to reef restoration</h2>



Coral restoration should not follow a one-size-fits-all model. Stylophora pistillata may benefit from assisted migration. Moving larvae or adult corals from healthy reefs to damaged ones could restore genetic diversity. 



However, such moves must be done carefully. Forcing new genes into a delicate reef might cause new problems.



Pocillopora verrucosa already benefits from strong natural connections. Protecting these migration routes may be enough.



Each coral species has its own needs. These needs are not the same. Conservation efforts should focus on these differences.



<h2 class="wp-block-heading" id="h-new-insights-for-coral-conservation">New insights for coral conservation </h2>



Coral reefs have an uncertain future. Their survival depends on how well we understand and protect the hidden connections between them.



The study, funded by the Australian Government’s Reef Trust and the Great Barrier Reef Foundation, brings new insights to reef science.



The research makes one thing clear: not all corals are the same. Some need protection close to home, while others depend on far-reaching connections. 



The study is published in the journal <a href="https://www.science.org/doi/10.1126/sciadv.adt2066" target="_blank" rel="noreferrer noopener">Science Advances</a>.



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Reef survival may depend on how far baby corals travel

Far below the ocean’s surface, the Great Barrier Reef hums...

A new executive order aimed at deregulating the U.S. seafood industry is raising red flags among scientists and policy experts. While the order claims to boost competitiveness and cut red tape, critics warn it could do more harm than good - weakening the very systems that protect seafood sustainability.



Scientists from <a href="https://www.ucsb.edu/">UC Santa Barbara</a> and the University of Washington outlined their concerns in a recent paper. They argue that the executive order misses the mark, prioritizing short-term gains over long-term stability.



<h2 class="wp-block-heading" id="h-inside-the-seafood-deregulation-order">Inside the seafood deregulation order</h2>



Signed in April 2025, the order - titled “Restoring American Seafood Competitiveness” - claims that U.S. <a href="https://www.earth.com/news/the-seafood-industry-has-been-hit-hard-by-the-covid-19-pandemic/">seafood markets</a> are held back by overregulation and unfair trade practices. It calls for reducing regulatory burdens, eliminating unsafe imports, and strengthening the <a href="https://www.earth.com/news/seafood-spoilage-hidden-dangers-in-the-cold-chain/">seafood supply chain</a>.



However, the researchers say the plan is moving too fast and with too little support. They describe it as a policy that risks unraveling decades of scientific progress.



“(It’s) a significant escalation in undoing federal regulatory frameworks, weakening scientific authority and deemphasizing aquaculture development,” said Halley Froehlich of UC Santa Barbara and Jessica Gephart of the University of Washington.



“Instead of reform, it’s dismantling regulations in a very short amount of time,” added Froehlich, the paper’s lead author.&nbsp;&nbsp;



<h2 class="wp-block-heading" id="h-noaa-s-role-under-threat">NOAA’s role under threat</h2>



The scientists point to cuts to the National Oceanic and Atmospheric Administration (NOAA) as a major concern. NOAA oversees roughly 500 commercial fishery stocks in the U.S. It plays a key role in managing, monitoring, and protecting marine resources.



Under the new directive, NOAA faces budget cuts, staff reductions, and tighter controls on communication. That’s a serious blow to its ability to coordinate sustainable fishing, especially across regions where fish migrate between countries.



“It’s quite problematic because NOAA is so central to how we manage our <a href="https://www.earth.com/news/bleaching-effect-coral-loss-threatens-fisheries-and-livelihoods/">fisheries</a>,” Froehlich said. “Data collection, monitoring, oversight, you name it, NOAA is part of that, and a really important part.”



<h2 class="wp-block-heading" id="h-the-plan-ignores-the-ocean-s-limits">The plan ignores the ocean’s limits</h2>



The executive order is supposed to help boost domestic seafood production. But the researchers argue that the ocean has limits - and we’re already close to reaching them.



“We are not going to get more out of the ocean,” Froehlich said. “We’re already near ‘peak fish,’ meaning maintenance and recovery of our stocks.”



Wild fisheries - both in the U.S. and globally - are already producing at or near their maximum sustainable levels. That leaves <a href="https://www.earth.com/news/aquaculture-now-produces-more-food-than-wild-fishing/">aquaculture</a> as the only real path for growth. 



However, the new order gives little attention to farmed seafood and offers even less support to the agencies that regulate it. The scientists call it a mismatch between promises and practical outcomes.



<h2 class="wp-block-heading" id="h-cutting-data-cutting-capacity">Cutting data, cutting capacity</h2>



One of the most troubling issues is the potential loss of data. The researchers warn that NOAA’s online databases, climate research, and monitoring tools may be defunded or decommissioned.



Without this data, managing fisheries becomes guesswork. It also makes it harder to prepare for climate-driven shifts in marine ecosystems.



“Without the data, expertise and capacity to study and understand these systems we run the risk of fishery collapses becoming more common and long-lasting,” the authors wrote.



<h2 class="wp-block-heading" id="h-trade-conflicts-and-mismatched-markets">Trade conflicts and mismatched markets</h2>



The executive order also makes assumptions about seafood markets that don’t align with reality. 



Much of the seafood farmed in the U.S. isn’t what consumers demand most. And a large portion of seafood caught in U.S. waters is processed overseas before being sold back into the domestic market.



If tariffs are imposed on imported or foreign-processed seafood, prices for high-demand products like <a href="https://www.earth.com/news/shrimp-crisis-alarming-virus-threatens-global-seafood-supplies/">shrimp</a> could rise sharply. Right now, only about 10% of shrimp eaten in the U.S. comes from domestic sources.



“In disrupting the market dynamics we do have, especially with trade wars with our trading partners, it’s likely that we’re going to have the opposite effect of creating opportunity long-term,” Froehlich said.



<h2 class="wp-block-heading" id="h-an-alternative-to-seafood-deregulation">An alternative to seafood deregulation </h2>



The paper was submitted as evidence in a recent hearing by the House Natural Resources Committee’s Water, Wildlife and Fisheries Subcommittee. The scientists hope their findings will influence how Congress approaches <a href="https://www.earth.com/news/seafood-will-help-feed-earths-future-population-of-10-billion/">seafood policy</a> moving forward.



“When it comes to any shifts in production, these high levels of uncertainty are not a beneficial thing to happen for the sector,” Froehlich said.



While deregulation may sound appealing to some, the authors argue that a stable, well-regulated system - backed by science and data - is what actually keeps seafood both sustainable and competitive. In their view, cutting corners now could cost the industry far more in the future.



The full study was published in the journal <a href="https://www.sciencedirect.com/science/article/pii/S0308597X25002106">Marine Policy</a>.



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Why seafood deregulation may hurt more than help

A new executive order aimed at deregulating the U.S. seafood...

In a fascinating new study, scientists documented 34 attempts by wild killer whales to give food to humans. These rare cases spanned four oceans and 20 years. Some happened near boats, others in open water or even from the shore. 



The events highlight the <a href="https://www.earth.com/news/killer-whales-use-kelp-to-massage-and-groom-each-other/">orcas</a>’ possible interest in humans and raise important questions about whale intelligence, communication, and social behavior.



“Orcas often share food with each other - it’s a prosocial activity and a way that they build relationships with each other,” said study lead author Jared Towers, of <a href="https://baycetology.org" target="_blank" rel="noreferrer noopener">Bay Cetology</a> in British Columbia, Canada. “That they also share with humans may show their interest in relating to us as well.”



<h2 class="wp-block-heading" id="h-social-lives-of-killer-whales">Social lives of killer whales</h2>



Orcas live some of the most complex social lives in the animal kingdom. They stick together in tight-knit family groups called pods, usually led by an older matriarch. 



These family units aren’t just casual gatherings - they’re lifelong bonds. Calves stay with their mothers for life, swimming, hunting, and <a href="https://www.earth.com/news/photographer-captures-killer-whales-wearing-fish-hats/">playing together</a>. 



In some regions, pods form larger communities or clans that share unique vocal dialects, kind of like cultural accents passed down through generations. This tight social structure helps them coordinate during hunts and <a href="https://www.earth.com/news/killer-whales-use-kelp-to-massage-and-groom-each-other/">protect each other</a> from threats.



But it’s not all business. Orcas socialize for the joy of it too. They engage in what clearly looks like play - tossing kelp, breaching dramatically, or nudging one another during underwater games. 



They form friendships beyond their pods and even flirt, showing preferences and personalities. These interactions suggest that orcas have emotional lives and a sense of identity.



<h2 class="wp-block-heading" id="h-what-orcas-gave-humans">What orcas gave humans</h2>



The 34 incidents involved six distinct populations of killer <a href="https://www.earth.com/news/ai-helps-humans-have-20-minute-conversation-with-humpback-whale-named-twain/">whales</a>. They offered humans a total of 18 species: six fish, five mammals, three invertebrates, two birds, one reptile, and even one piece of seaweed.



In 97 percent of these cases, the orcas waited for a human response. Some hovered for several minutes. 



On several occasions, they tried again when the humans ignored or returned the offering. In two especially curious cases, whales retrieved birds after humans returned them, only to offer them again.



This behavior could be a form of interspecies curiosity, communication, or even social learning. As the authors suggest, these events might represent "generalized altruism" - an advanced trait observed in only a few social animals.



<h2 class="wp-block-heading" id="h-exploration-more-than-play">Exploration more than play</h2>



Though play was observed in 38 percent of the interactions, the researchers argue most cases were not playful. The age of the whales varied widely, and many offered whole, fresh prey. 



In over 75 percent of ignored cases, the whales later used the prey for themselves or their group. This suggests the offerings had purpose and value, not just entertainment.



Curiosity-driven behavior, distinct from play, seemed a stronger motivator. As the study explains, animals often explore to reduce uncertainty. 



Offering food to humans might help orcas learn how we respond, just as they would with unfamiliar members of their own <a href="https://www.earth.com/news/whales-blow-bubble-smoke-rings-near-humans-to-communicate/">species</a>.



<h2 class="wp-block-heading" id="h-deep-social-intelligence-at-work">Deep social intelligence at work</h2>



Some whales returned the same item to humans multiple times. Others acted in pairs or small groups. 



Most of the 34 events involved a single whale separating from a larger group. This suggests the act was not for show. Rather, it might reflect the whale's individual decision to interact.



Interestingly, killer <a href="https://www.earth.com/news/how-dolphin-brains-evolved-to-see-underwater-by-using-sound-echolocation/">whales</a> have also been documented cooperating with human fishers in places like Australia and Russia. The authors noted that this history could influence modern interactions, especially as human activity increases near their habitats.



<h2 class="wp-block-heading" id="h-whales-may-view-humans-as-companions">Whales may view humans as companions</h2>



Killer whales rank second only to humans in brain-to-body ratio. They also show advanced emotional and social behavior. 



These traits support complex social learning, reciprocal behavior, and possibly even empathy.



“Offering items to humans could simultaneously include opportunities for killer whales to practice learned cultural behavior, explore or play and in so doing learn about, manipulate or develop relationships with us,” the researchers wrote.



<h2 class="wp-block-heading" id="h-humans-should-not-approach-whales">Humans should not approach whales</h2>



Despite the remarkable nature of these encounters, the researchers urge caution. Orcas can show complex and sometimes unpredictable behavior. 



While no wild killer whale has killed a person, some interactions have been intense. They warn against seeking out such encounters or encouraging the behavior without proper permissions.



Most of these whales belonged to populations that hunt near the surface and share prey frequently. 



No deep-water, fish-only populations were involved. This suggests that cooperative surface hunting may lead to more frequent and visible interspecies interactions.



<h2 class="wp-block-heading" id="h-complex-minds-of-whales-and-humans">Complex minds of whales and humans</h2>



The findings challenge our assumptions about human-animal relationships. If orcas are experimenting with ways to relate to us, it means they recognize us not as threats, but as potential social partners.



These whales are not just predators. They are thinkers, observers, and maybe, in some way, explorers of culture, curiosity, memory, learning, and emotion. 



Their actions suggest complex minds in both whales and humans, capable of choice, empathy, and communication.



The study is published in the <a href="https://psycnet.apa.org/fulltext/2026-29805-001.html" target="_blank" rel="noreferrer noopener">Journal of Comparative Psychology</a>. 



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Killer whales are attempting to bond with humans, according to scientists

In a fascinating new study, scientists documented 34 attempts by...

Plankton,Are,Organisms,Drifting,In,Oceans,And,Seas.,Zooplankton.

They may be small, but zooplankton like copepods, krill, and salps are pulling serious weight when it comes to storing carbon in the Southern Ocean. 



Every year, billions of these tiny animals migrate from the surface to deep waters. In doing so, they help trap tens of millions of tons of <a href="https://www.earth.com/news/how-the-ocean-holds-carbon-hidden-mechanisms-revealed/">carbon</a> far below the ocean surface.



<h2 class="wp-block-heading" id="h-a-new-look-at-ocean-carbon-storage">A new look at ocean carbon storage </h2>



Until recently, scientists believed most of the carbon stored in the Southern Ocean sank slowly through the water column, tied up in the waste left by larger zooplankton feeding near the surface. But a new study offers a clearer - and more surprising - picture.



The research was led by experts at the Institute of Oceanology, Chinese Academy of Sciences, the Plymouth Marine Laboratory, the <a href="https://www.plymouth.ac.uk/">University of Plymouth</a>, and the British Antarctic Survey 



The study is the first to measure how much carbon is pulled down by the “seasonal migrant pump.” 



In this process, zooplankton descend each autumn to depths below 1,640 feet (500 meters), stay there for months, and release carbon into the deep ocean through respiration and death.



<h2 class="wp-block-heading" id="h-tiny-swimmers-store-carbon">Tiny swimmers store carbon</h2>



The team analyzed thousands of net haul samples collected over the past century from across the <a href="https://www.earth.com/news/carbon-storage-mystery-emerges-in-the-southern-ocean/">Southern Ocean</a>. The records helped build a massive database that tracks how deep and how consistently these creatures migrate each year.



What the researchers found is eye-opening: this seasonal migration injects about 65 million tons of carbon annually into the deep ocean. This enormous amount of carbon could otherwise stay in the <a href="https://www.earth.com/news/a-weaker-ocean-will-release-more-carbon-into-the-atmosphere/">atmosphere</a>, contributing to global warming.



“We find that copepods significantly dominate carbon storage overwinter,” said Dr. Jen Freer. “This has big implications as the ocean warms and their habitats may shift."



<h2 class="wp-block-heading" id="h-carbon-storage-in-the-southern-ocean">Carbon storage in the Southern Ocean </h2>



<a href="https://www.earth.com/news/tiny-crustaceans-have-what-it-takes-to-survive-climate-change/">Copepods</a> - small, shrimp-like crustaceans - are the main drivers of this deep-sea carbon delivery system. They’re responsible for about 80 percent of the total carbon flux linked to the seasonal migrant pump. <a href="https://www.earth.com/news/antarctic-krill-are-natures-unexpected-carbon-warriors/">Krill</a> contribute another 14 percent, while salps account for six percent.



These numbers matter. The Southern Ocean absorbs about 40 percent of human-released CO2 that ends up in the oceans.



That’s a huge chunk, but until now, models didn’t factor in this seasonal migration. They focused mostly on passive sinking - when detritus like feces or dead material falls through the water.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/zooplankton_mesozooplankton_carbon_southern-ocean_credit-LnO_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/zooplankton_mesozooplankton_carbon_southern-ocean_credit-LnO_1s.webp" alt="A schematic representation of our calculations of the seasonal vertical carbon transport by mesozooplankton, krill, and salps during winter of the Southern Ocean. The values for SVMP flux are totals for mesozooplankton, krill, and salps and the upper and lower ranges for POC flux refer to annual estimates based on sediment traps and earth system models. Credit: Limnology and Oceanography" class="wp-image-1976081"/></a><figcaption class="wp-element-caption">A schematic representation of our calculations of the seasonal vertical carbon transport by mesozooplankton, krill, and salps during winter of the Southern Ocean. The values for SVMP flux are totals for mesozooplankton, krill, and salps and the upper and lower ranges for POC flux refer to annual estimates based on sediment traps and earth system models. Click image to enlarge. Credit: Limnology and Oceanography</figcaption></figure>



Unlike the slow sinking process, the seasonal migrant pump is a direct injection. And it has another upside: it keeps essential nutrients like iron in the upper layers, where they support marine life.



That means zooplankton aren’t just removing carbon - they’re doing it efficiently, without robbing the ocean’s surface of the nutrients needed to keep ecosystems going.



<h2 class="wp-block-heading" id="h-warming-shifts-zooplankton-paths">Warming shifts zooplankton paths</h2>



The Southern Ocean is changing. Climate warming is shifting the range of species like krill and copepods, and that could reshape how much carbon gets locked away each year.



“The study shows the 'seasonal migrant pump' as an important pathway of natural carbon sequestration in polar regions,” said Dr. Katrin Schmidt. “Protecting these migrants and their habitats will help to <a href="https://www.earth.com/news/can-we-mitigate-climate-change-with-deep-ocean-storage/">mitigate climate change</a>."



The research suggests that climate models are in urgent need of an update. Current Earth System Models don’t include this zooplankton-driven mechanism, which means they may be missing a key part of the ocean’s carbon story.



“This study is the first to estimate the total magnitude of this carbon storage mechanism,” said Professor Angus Atkinson. “It shows the value of large data compilations to get an overview of the relative importance of carbon storage mechanisms."



<h2 class="wp-block-heading" id="h-small-creatures-global-impact">Small creatures, global impact</h2>



By building on nearly a century of data and contributions from scientists in China, the UK, and Canada, the study provides one of the clearest pictures yet of how small marine animals influence global climate through ocean carbon storage.



“Our work shows that zooplankton are unsung heroes of carbon sequestration,” said study lead author Dr. Guang Yang. “Their seasonal migrations create a massive, previously unquantified carbon flux - one that models must now incorporate."



Protecting the Southern Ocean means more than safeguarding <a href="https://www.earth.com/news/biodiversity-leaks-conservation-efforts-may-shift-harm-elsewhere/">biodiversity</a>. It means defending one of the planet’s most efficient natural carbon storage systems - powered by creatures smaller than a grain of rice.



The full study was published in the journal <a href="https://aslopubs.onlinelibrary.wiley.com/doi/10.1002/lno.70120">Limnology and Oceanography</a>.



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These tiny creatures play an outsized role in Southern Ocean carbon storage

They may be small, but zooplankton like copepods, krill, and...

Virginia faces a stubborn enemy: the spotted lanternfly (SLF). These invasive insects damage trees, crops, and gardens by feeding on plant sap and leaving behind sticky honeydew. A research team led by Assistant Professor Scotty Yang at Virginia Tech has discovered an unexpected helper in the battle against this pest: ants.



Yang and his team found that ants, drawn to honeydew, can carry traces of lanternfly DNA in their bodies. By analyzing the ants, scientists can now detect whether the <a href="https://www.earth.com/news/fish-swim-in-schools-by-stacking-like-ladder-rungs/">pest</a> has reached an area, even without spotting the insect directly.



<h2 class="wp-block-heading" id="h-ants-collect-lanternfly-dna">Ants collect lanternfly DNA</h2>



The research is based on environmental DNA, or eDNA. This approach collects genetic material that organisms leave behind in their surroundings. 



Spotted lanternflies leave DNA in their sugary waste, which ants readily consume. Scientists then apply a lab technique called polymerase chain reaction, or PCR, to identify SLF DNA inside the ants.



“Ants are nature’s sugar seekers,” Yang said. “If there’s even a tiny drop of honeydew left behind by a spotted lanternfly, ants are likely to find it.”



Yang’s team named the method “antDNA.” Even a single meal of honeydew lets <a href="https://www.earth.com/news/swarm-intelligence-ants-can-anticipate-obstacles-and-plan-ahead/">ants</a> retain the lanternfly's DNA for up to five days. Because ants roam widely, this method can detect SLF activity from as far as 100 meters from the infestation.



<h2 class="wp-block-heading" id="h-field-tests-across-virginia">Field tests across Virginia</h2>



Researchers tested the method at three Virginia sites: Salem, Lynchburg Site 1, and Lynchburg Site 2. These locations represented low, medium, and high lanternfly densities. 



At each site, they placed honey-baited lure stations along transects, attracting ants with cotton balls soaked in honey.



The Salem site showed a 46.7 percent positive rate for SLF DNA. Lynchburg Site 1 and Site 2 showed 62.1 percent and 62.5 percent, respectively. Most stations attracted ants within 30 minutes, proving the method’s ease of use.



The study also tested ants from nine species. SLF DNA was found even in ants that had not directly fed on honeydew, likely due to food sharing within <a href="https://www.earth.com/news/selfish-dna-in-a-few-ants-can-change-the-behavior-of-the-entire-colony/">colonies</a>. This behavior, known as trophallaxis, helps spread the DNA signal among nestmates.



<h2 class="wp-block-heading" id="h-ants-outperform-other-lanternfly-detectors">Ants outperform other lanternfly detectors</h2>



The antDNA technique works across landscapes and does not depend on the pest being visible. Unlike other methods, it does not require water, filtration, or special storage. Ants can be preserved in ethanol without refrigeration, reducing the burden on field teams.



Ants are present in nearly every habitat, from forests to cities. The collection setup is simple and inexpensive. The ants’ ability to hold liquid in their crop allows the DNA to stay detectable longer than in typical surface samples. 



The study confirmed that DNA from honeydew lasts longer than DNA from insect tissue, making honeydew a more stable source.



<h2 class="wp-block-heading" id="h-importance-of-early-detection">Importance of early detection</h2>



Spotted lanternflies harm many plants, including grapevines, hardwoods, and hops. As they feed, they weaken plants and coat them in honeydew. This sticky substance promotes sooty mold, which further harms plant health. 



Early detection is critical because removing the pest becomes harder once it spreads. Current surveillance efforts rely on human sightings of the insect or its egg masses. These sightings often occur only when the population has already grown. 



The ant surveillance method allows early detection of lanternfly species even in low-density zones and inaccessible areas.



<h2 class="wp-block-heading" id="h-scaling-up-and-looking-forward">Scaling up and looking forward</h2>



Yang and his team are now working on a portable test kit for use in the field. This will allow real-time molecular testing without needing a full lab. Faster results mean quicker action against the pest.



“One of the biggest advantages of using ants is that they live almost everywhere, such as forests, farms, cities - you name it,” Yang said. “Their constant search for food makes them ideal frontline samplers for spotted lanternfly DNA.”



This approach offers a new way to watch for invasive species like lanternflies using ants, without depending on visual surveys. It opens up possibilities for surveillance that is fast, flexible, and low-cost.



<h2 class="wp-block-heading" id="h-ants-may-detect-other-pests-like-lanternflies">Ants may detect other pests like lanternflies</h2>



The method could be expanded to track other pests. Many <a href="https://www.earth.com/news/how-many-ants-live-on-earth-at-any-point-in-time-total-number-is-astounding/">insects</a> excrete honeydew, and ants can pick up their DNA too. This opens the door for broader pest detection strategies using the same principle.



Ants, in their natural role as sugar hunters, may become an essential part of protecting crops, forests, and native ecosystems. With antDNA, researchers are tapping into nature’s own behaviors to find smarter ways of monitoring invasive threats.



The study is published in the journal <a href="https://scijournals.onlinelibrary.wiley.com/doi/10.1002/ps.8814" target="_blank" rel="noreferrer noopener">NeoBiota</a>.



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How ants could help stop the tree-killing lanternfly

Virginia faces a stubborn enemy: the spotted lanternfly (SLF). These...

In the wild, social lives shape survival. For female chimpanzees, bonds with others aren't just emotional glue. They are critical for keeping babies alive. 



A new study of wild eastern chimpanzees in Gombe National Park finds that social integration predicts whether a newborn survives, even when no close kin is around.



<h2 class="wp-block-heading" id="h-chimpanzees-with-strong-social-bonds">Chimpanzees with strong social bonds</h2>



Female <a href="https://www.earth.com/news/laughter-lifts-bonobo-moods-offering-clues-to-human-emotion/">chimps</a> are often the ones who leave their birth group. That means most do not live near their mothers or sisters. Still, those who manage to build friendships with other females raise more babies to weaning age.



“In species where females live in groups with their sisters and mothers, it’s less surprising that female sociality is beneficial,” said <a href="https://scholars.duke.edu/person/joseph.feldblum" target="_blank" rel="noreferrer noopener">Joseph Feldblum</a>, lead author and research professor at Duke. 



“But female chimps don’t usually have that. They are also less gregarious than males, so the fact that forming strong social connections still matters is striking.”



<h2 class="wp-block-heading" id="h-babies-of-social-chimpanzees">Babies of social chimpanzees </h2>



The team analyzed 37 years of detailed records from 37 mothers and 110 offspring. Using a composite sociality index (CSI), they tracked how much time females spent associating or grooming others before giving birth.



Their best model showed that higher CSI scores, especially with other <a href="https://www.earth.com/news/baby-talk-may-explain-what-sets-humans-apart-from-apes/">females</a>, greatly increased infant survival to age one and even to age five. The effect held even after excluding mothers who died shortly after giving birth.



A female with a CSI score twice the average had a 95 percent chance of her baby surviving the first year. For those below average, this dropped to 75 percent. 



Among females without any close kin, the trend was stronger. A single unit rise in sociality increased survival odds by over 17 times.



<h2 class="wp-block-heading" id="h-kinship-and-male-alliances">Kinship and male alliances </h2>



The researchers ran extra tests to see if the benefit was just from living with relatives. It was not. They also checked if relationships with <a href="https://www.earth.com/news/from-rumbles-to-rituals-scientists-map-the-cultures-of-the-animal-kingdom/">males</a> helped. That also came up short.



“That tells us it’s not just about being born into a supportive family,” said Feldblum. “These are primarily social relationships with non kin.”



Even when female kin were present, they had no direct effect on offspring survival. Instead, they raised the chance that a mother had strong friendships. But it was those friendships, not the family ties, that made the difference.



<h2 class="wp-block-heading" id="h-social-ties-remain-stable-over-time">Social ties remain stable over time</h2>



The benefits of bonding were not a one time fluke. Females who were social before birth stayed social after birth too. Their social worlds remained steady. 



“Our results don’t prove causation, but they point to the value of being surrounded by others who support you, or at least tolerate you,” said Feldblum.



This was not the case for bonds with males. Social connections between male and female chimpanzees were less stable and showed no link to baby survival.



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



How do these friendships help? The exact mechanism remains uncertain. Social bonds might protect chimpanzee mothers from aggression. They could mean better access to food. Friendships might even prevent infanticide.



Earlier studies in this same group of chimps estimated that infanticide by other females may cause 3.5 percent to 19 percent of deaths in the first year. <a href="https://www.earth.com/news/social-curiosity-starts-young-and-helps-us-survive/">Social</a> mothers may face less of that risk.



More research is needed, but one thing is clear. Socially connected females stay in better shape, which could boost prenatal health. Unlike rank or dominance, which did not correlate with survival during this study window, sociality kept its value.



<h2 class="wp-block-heading" id="h-social-chimps-mirror-humans">Social chimps mirror humans</h2>



Though females often move away from family, they form lasting ties with unrelated females. The Gombe chimps mirror women in human patrilocal societies, who build networks after moving for marriage.



“We humans are remarkably collaborative and cooperative. We cooperate at scales that are pretty much unique in the animal kingdom,” said Feldblum. 



“Human females who don’t have access to kin, for example because they moved to a new city or village, are still able to form strong bonds that can benefit them.”



This study adds to the growing body of evidence that friendship matters. In baboons, dolphins, and horses, social bonds also improve reproductive success. In chimps too, strong bonds give babies a better chance at life.



Studying these dynamics in our closest relatives helps us understand our own nature. Like chimps, human survival does not just depend on strength or status. It depends on others. 



The study is published in the journal <a href="https://www.sciencedirect.com/science/article/pii/S2589004225011241" target="_blank" rel="noreferrer noopener">iScience</a>.



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Babies of social chimpanzee mothers are more likely to survive

In the wild, social lives shape survival. For female chimpanzees,...

Gorillas, often thought of as ground dwellers, spend much more time in the trees than previously assumed. This finding from the Max Planck Institute challenges long-standing ideas about the anatomy and evolution of gorillas.



Western and Bwindi mountain <a href="https://www.earth.com/news/gorillas-are-digging-for-a-surprising-food-in-the-jungle-soil/">gorillas</a>, studied across Gabon and Uganda, were observed over many years. Even the largest males, weighing up to 170 kg, showed substantial tree use. 



Adult females in Loango spent 34% of their time in trees, while Bwindi females clocked 21%. That is a huge jump from the 7% figure for Virunga gorillas.



Study lead author Dr. Martha M. Robbins is a zoologist in the Department of Primate Behavior and Evolution at the <a href="https://www.eva.mpg.de/index/">Max Planck Institute</a> for Evolutionary Anthropology.



“Adult females spent 20% to 30% of their time in the trees, while silverbacks spent 18% to 20% of their time being arboreal, which is much more than 2 to 7% found previously in the Virunga mountain gorillas,” said Dr. Robbins.



<h2 class="wp-block-heading" id="h-different-gorillas-different-tree-habits">Different gorillas, different tree habits</h2>



The Virunga population shaped our early understanding of <a href="https://www.earth.com/news/some-gorillas-get-sick-from-being-too-social/">gorilla</a> habits. These highland gorillas live in fruit-scarce zones and rarely climb. But the new study included data from five groups in Bwindi and one in Loango, totaling nearly 5,200 observation days.



The findings are clear: tree use varies widely between populations. Even juveniles and subadults in Bwindi and Loango spent 32% to 43% of their time in trees - double the rate seen in Virunga’s younger gorillas.



The researchers also found that body size plays a role but does not prevent tree climbing. 



“This demonstrates that the large body size of gorillas is not necessarily a limiting factor to tree climbing and that gorillas can be just as arboreal as some chimpanzee populations,” said co-author Rhianna Drummond-Clarke.



<h2 class="wp-block-heading" id="h-climbing-is-not-just-about-fruit">Climbing is not just about fruit</h2>



The researchers expected fruit to be the main driver behind climbing. While gorillas did climb more while eating fruit, the full story is more complex. In Loango, adult females were more arboreal when eating leaves than fruit. In Bwindi, the reverse was true.



Even silverbacks, the heaviest individuals, climbed trees to eat fruit. At Bwindi, silverbacks were arboreal 82% of the time they ate fruit. But fruit formed just 14% of their diet, meaning most of their tree time involved eating leaves.



At Loango, gorillas often ate fallen fruit from the ground. This shows fruit-eating can be a terrestrial act too. Meanwhile, western gorillas also ate lots of tree leaves, about 30% of their diet, driving folivorous tree use, similar to some monkeys.



<h2 class="wp-block-heading" id="h-feeding-is-the-main-reason-to-climb">Feeding is the main reason to climb</h2>



What were the <a href="https://www.earth.com/news/male-infertility-humans-linked-same-genes-gorilla-small-penises/">gorillas</a> doing in trees? Mostly feeding. Adult female gorillas were far more likely to climb while feeding than when resting or traveling.



Even when eating nonfruit, Loango females climbed more than Bwindi ones. This likely reflects differences in diet and foraging strategy. The energy payoff from fruit seems to outweigh the climbing cost, especially for massive silverbacks.



Also, Loango females were heavier climbers than their Bwindi peers when not eating fruit. This surprising reversal shows that even leaf-seeking gorillas may spend considerable time off the ground.



<h2 class="wp-block-heading" id="h-what-this-means-for-ape-evolution">What this means for ape evolution</h2>



These results have big implications. <a href="https://www.earth.com/news/most-endangered-primate-species-identified-in-new-report/">Gorillas</a> have long been labeled as terrestrial because of their bulk and plant-heavy diets. But that view no longer holds. The study shows gorilla arboreality spans all life stages, from infants to adults.



That shift affects how we interpret the fossil record. Gorilla-like bones have been taken to suggest ground-based life. But frequent tree climbing changes the picture. 



“We demonstrate that large body size and a largely folivorous diet in apes are also consistent with frequent arboreality,” noted the study authors.



Studies of limb proportions and bone strength now suggest a range, from more tree-based western gorillas to more ground-based Virunga ones. 



This means our models of ancient human relatives may need adjustment. Gorilla-like features may not imply they lived solely on the ground.



<h2 class="wp-block-heading" id="h-gorillas-are-tree-climbers-not-just-walkers">Gorillas are tree climbers, not just walkers</h2>



Gorillas are not just forest-floor giants. They climb often and for various reasons. From feeding on leaves to exploring the canopy, these behaviors offer key insights into how apes, including humans, evolved.



Future research may look into how such large animals navigate trees. They might distribute their weight across branches or use special movement strategies, similar to orangutans or chimpanzees. 



This research opens new doors in our understanding of ape mobility and evolutionary history.



The study is published in the journal <a href="https://www.cell.com/current-biology/fulltext/S0960-9822(25)00590-1" target="_blank" rel="noreferrer noopener">Current Biology</a>.



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Gorillas spend much more time in trees than we previously thought

Gorillas, often thought of as ground dwellers, spend much more...

When humans burst into laughter together, moods lift almost automatically. New research shows that a similar boost happens in our closest cousins.



An international team led by <a href="https://bloomington.iu.edu/">Indiana University</a> scientists has discovered that <a href="https://www.earth.com/news/bonobos-group-cohesion-common-enemy-effect-do-not-kill-inside-their-species/">bonobos</a> become more upbeat after hearing the giggles of their companions. This finding pushes the evolutionary history of positive emotions back millions of years.



<h2 class="wp-block-heading" id="h-laughter-changed-ape-choices">Laughter changed ape choices</h2>



To explore laughter’s influence, the researchers designed a cognitive-bias test often used in animal psychology to gauge optimism or pessimism.



First, they trained bonobos at the <a href="https://www.apeinitiative.org/">Ape Initiative</a> in Des Moines, Iowa, to recognize two kinds of boxes: black ones that always contained a delicious snack and white ones that were always empty.



Once the apes consistently chose black and ignored white, the experimenters introduced a third, ambiguous gray box. They then played one of two sounds: recorded bonobo laughter or a neutral control noise.



“We know that other apes, like chimpanzees, have contagious laughter during play," said lead author Sasha Winkler, a primatologist at <a href="https://duke.edu/">Duke University</a>. "We were wondering if that behavior could be explained by positive emotions produced from the sound itself.” 



If the bonobos felt a surge of good feeling after hearing laughter, the team expected them to treat the uncertain gray box as if it were the rewarding black one.



That is exactly what happened. “Think of it like the rose-colored glasses effect,” Winkler said. “The bonobos were much more likely to approach the gray boxes after hearing laughter, treating them like the rewarded boxes, and indicating a more optimistic expectation of finding a treat.”



<h2 class="wp-block-heading" id="h-tracing-optimism-to-our-ancestors">Tracing optimism to our ancestors</h2>



This study is the first experimental proof that great-ape laughter can shift mood and cognition the way human laughter does.



“The tendency to behave more optimistically after hearing laughter suggests that the sound alone induced a positive emotional state in bonobos,” said senior author Erica Cartmill, the director of Indiana University’s Cognitive Science Program.



“This is the first study of which we're aware to measure a positive affect shift in nonhuman primates from a brief experimental intervention.”



Great apes -&nbsp; bonobos, <a href="https://www.earth.com/news/what-wild-chimpanzees-can-teach-us-about-parenting/">chimpanzees</a>, gorillas, orangutans - all emit play calls that acoustically resemble human chuckles. Earlier work tied those sounds to a common evolutionary origin. The new findings add a cognitive twist.



“Our results suggest that laughter in other apes shares not only phylogenetic and behavioral similarities with human laughter but also perhaps some of the same cognitive-emotional underpinnings,” Winkler noted.



“This emotional contagion appears to have been present in the primate lineage long before the evolution of language.”



<h2 class="wp-block-heading" id="h-laughter-empathy-and-apes">Laughter, empathy, and apes</h2>



Emotional contagion is often described as a foundational element of <a href="https://www.earth.com/news/little-benjamina-the-oldest-evidence-of-social-empathy-in-humans/">empathy</a> - the capacity to share another’s feelings. As Winkler put it, “studies like ours can help to untangle the evolutionary building blocks of empathy, communication, and cooperation in humans.”



By revealing that a simple vocal cue can brighten outlooks in bonobos, the research suggests that the mechanisms linking social sound to positive mood were already in place in a common ancestor millions of years ago.



Cartmill added that the work answers a long-standing bias in emotion research. “Our emotions influence many aspects of cognition, including memory, attention, and decision-making, but research has historically focused on negative emotions with clear behavioral correlates, like <a href="https://www.earth.com/news/brain-pathway-discovered-that-suppresses-fear/">fear</a> and aggression.”



“We wanted to better understand the relationship between positive affect and cognition in our closest living relatives.”



<h2 class="wp-block-heading" id="h-kanzi-and-the-future-of-empathy">Kanzi and the future of empathy</h2>



The experiments involved four bonobos, including the celebrated language-using ape Kanzi, who recently passed away.



“I feel incredibly grateful to have had the opportunity to work with Kanzi while he was still alive,” Winkler said. 



“We hope this brings greater public awareness of the remarkable similarities between us and bonobos, who are an endangered species. We have so much to learn from these incredible animals.”



Future studies will test whether laughter exerts similar cognitive effects in chimpanzees and other primates. They will also explore how social context - for example, hearing laughs from friends versus strangers - modulates optimism.



For now, the discovery that bonobo giggles brighten expectations highlights a shared emotional heritage and hints that a simple laugh has been boosting group spirits since long before humans walked the Earth.



The study is published in the journal <a href="https://www.nature.com/articles/s41598-025-02594-8">Nature Scientific Reports</a>.



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Laughter lifts bonobo moods, offering clues to human emotion

When humans burst into laughter together, moods lift almost automatically....

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...

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