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

The Cambrian period, around 520 million years ago, was an age of experimentation. Life in the seas was trying out every possible body plan, searching for combinations that worked. 



One line of creatures, the euarthropods, hit on a winner: segmented bodies, paired jointed limbs, and a knack for tweaking those limbs into claws, feelers, and walking legs. That design still powers today’s insects, spiders, and crabs.



Until now, most clues to the early stages of that success came from flattened impressions squeezed by eons of mud and rock. They showed outlines but kept their secrets sealed. 



A newly described fossil larva named Youti yuanshi no bigger than a poppy seed and preserved in three dimensions, has flung those doors open.



This research was led by Dr. Martin Smith from <a href="https://www.durham.ac.uk/" target="_blank" rel="noreferrer noopener">Durham University</a>. His expertise and intuition led to this exceptional discovery, which is considerably reshaping our understanding of insect evolution.



<h2 class="wp-block-heading" id="h-youti-yuanshi-and-insect-evolution">Youti yuanshi and insect evolution</h2>



The fossil in focus, Youti yuanshi, takes us on a thrilling journey back to the Cambrian period, a time when the major animal groups we know today were <a href="https://www.earth.com/news/evolution-is-both-predictable-and-random/" target="_blank" rel="noreferrer noopener">first evolving</a>.



This fossil falls under the group of arthropods, which includes modern insects, spiders and crabs. 



What sets this fossil apart is its exceptional preservation of internal organs, offering a close-up view of life forms from a time unimaginable to us.



Using the cutting-edge synchrotron X-ray tomography at <a href="https://www.diamond.ac.uk/Home.html" target="_blank" rel="noreferrer noopener">Diamond Light Source</a>, the UK's national synchrotron science facility, the research team was able to generate 3D images of this miniature marvel.



They unveiled brain regions, digestive glands, a rudimentary circulatory system and even traces of nerves supplying the larva’s simple legs and eyes.



<h2 class="wp-block-heading" id="h-3d-view-of-youti-yuanshi-guts">3D view of Youti yuanshi guts</h2>



This research allows us to see inside one of the earliest arthropod ancestors. It's a revelation of sort: these early arthropod-relatives had an unexpectedly advanced anatomy.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.nature.com/articles/s41586-024-07756-8/figures/1" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2024/08/euarthropod-larva_youti-yuanshi_fossil_guts-preserved_credit-Nature_1s.webp" alt="Anatomical overview of Youti yuanshi - organs of a Cambrian euarthropod larva. Credit: Nature" class="wp-image-1973987"/></a><figcaption class="wp-element-caption">Anatomical overview of Youti yuanshi - organs of a Cambrian euarthropod larva. Click image for more details. Credit: Nature</figcaption></figure>



"When I used to daydream about the one fossil I’d most like to discover, I’d always be thinking of an arthropod larva, because developmental data are just so central to <a href="https://www.earth.com/news/insect-flight-is-powered-by-an-extraordinary-structure/" target="_blank" rel="noreferrer noopener">understanding their evolution</a>. But larvae are so tiny and fragile, the chances of finding one fossilized are practically zero - or so I thought!" Dr. Smith enthused.



"I already knew that this simple worm-like fossil was something special, but when I saw the amazing structures preserved under its skin, my jaw just dropped - how could these intricate features have avoided decay and still be here to see half a billion years later?”



<h2 class="wp-block-heading" id="h-overview-of-insect-evolution">Overview of insect evolution</h2>



Dr. Katherine Dobson from the <a href="https://www.strath.ac.uk/" target="_blank" rel="noreferrer noopener">University of Strathclyde</a>, another key contributor to this study, shared her amazement at the near-perfect preservation of the ancient larva.



"It’s always interesting to see what’s inside a sample using 3D imaging, but in this incredible tiny larva, natural fossilization has achieved almost perfect preservation," she states.



This ancient larva holds the key to solving a myriad of questions on the evolution of multi-limbed creatures. 



For instance, the fossil reveals an ancestral ‘protocerebrum’ brain region that was pivotal in our journey towards complex, segment-headed creatures.



The observations from this fossil help trace the path that led modern arthropods to gain their remarkable anatomical complexity and diversity. 



Moreover, these findings fill a crucial gap in our understanding of how the arthropod body plan originated during the <a href="https://www.earth.com/news/animals-exist-today-ediacaran-period-earth-weak-magnetic-field/" target="_blank" rel="noreferrer noopener">Cambrian Explosion of life</a>.



<h2 class="wp-block-heading" id="h-why-does-any-of-this-matter">Why does any of this matter?</h2>



The discovery of Youti yuanshi not only sheds light on the evolution of early arthropods but also prompts broader reflections on <a href="https://www.earth.com/news/nighttime-buzz-insect-activity-increases-by-31-4-at-night/" target="_blank" rel="noreferrer noopener">biodiversity</a> itself.



Understanding the anatomical features and adaptations of extinct species provides context for the diverse forms of life we observe today. 



This fossil acts as a reminder of the intricate web of evolutionary relationships that has shaped the myriad species inhabiting our planet.



As we explore these connections, we deepen our appreciation for the resilience and adaptability of life throughout the ages, underscoring the importance of preserving our current ecosystems.



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



The insights from Youti yuanshi are opening up exciting new paths for research, especially in fields like evolutionary biology, paleontology, and developmental biology.



Researchers are eager to dig deeper into Cambrian period fossils, hoping to find more specimens that shed light on the complex details of early life forms. 



Plus, the techniques used in this study, like synchrotron X-ray tomography, could be applied to other fossils, helping us discover even more about the milestones in the tree of life. 



This poppy-seed fossil proves that even the tiniest finds can overturn years of assumption. 



Future digs, armed with ever-sharper imaging tools, will no doubt uncover more diminutive ambassadors from deep time, each ready to whisper another chapter of our planet’s earliest animal saga.



The fossil is now housed at <a href="https://english.ynu.edu.cn" target="_blank" rel="noreferrer noopener">Yunnan University</a> in China, its original discovery site. This eye-opening research emphasizes the crucial role of fossils in understanding our roots and the <a href="https://www.earth.com/news/how-life-and-environment-co-evolved-over-500-million-years/" target="_blank" rel="noreferrer noopener">evolution of life on Earth</a>.



The study is published in the journal <a href="https://www.nature.com/articles/s41586-024-07756-8" target="_blank" rel="noreferrer noopener">Nature</a>.



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520-million-year-old fossil discovered with brains and guts still intact, stunning the lead scientist

The Cambrian period, around 520 million years ago, was an...

Take a sip of cabernet and your tongue might feel as if it's being scraped by coarse paper, while another vintage wine may glide across your mouth. According to chemists, this contrast in wine texture isn't just about how much tannin is present, but rather the exact molecular <a href="https://www.earth.com/news/wines-may-develop-new-tastes-as-climate-patterns-change/" target="_blank" rel="noreferrer noopener">structure</a> of the tannins themselves.



The new <a href="https://pubmed.ncbi.nlm.nih.gov/40377541/" target="_blank" rel="noreferrer noopener">Condensed Tannin Fragmentation Fingerprinting method</a> tags every tannin fragment as it shatters inside a high‑resolution <a href="https://www.broadinstitute.org/technology-areas/what-mass-spectrometry" target="_blank" rel="noreferrer noopener">mass spectrometer</a>. The method transforms an invisible chemical jumble into a sortable library of flavor clues that winemakers can read like sheet music.



The peer‑reviewed study was directed by <a href="https://foodscience.psu.edu/directory/mtk5407" target="_blank" rel="noreferrer noopener">Misha Kwasniewski</a>, associate research professor of fermented beverage science and technology at <a href="https://agsci.psu.edu/" target="_blank" rel="noreferrer noopener">Penn State’s College of Agricultural Sciences</a>.



<h2 class="wp-block-heading" id="h-tannins-affect-wine-texture">Tannins affect wine texture</h2>



<a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC12111099/" target="_blank" rel="noreferrer noopener">Procyanidins</a> are branched chains of the <a href="https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/flavanols" target="_blank" rel="noreferrer noopener">flavanol catechin</a> that can run from two to well over a dozen units, and the twists, bonds, and branching angles within those chains set how tightly the molecules clamp onto salivary proteins. 



Longer, more entangled chains strip away lubrication faster, so the same <a href="https://www.earth.com/news/how-grapes-became-wine-in-italy-over-7000-years/" target="_blank" rel="noreferrer noopener">chemical</a> family can create either a silky glide or a chalky drag across the gums.



When tannins bind those proteins, the resulting complexes lose solubility and scatter light - roughening tissue surfaces and amplifying the tactile signal drinkers describe as <a href="https://pubmed.ncbi.nlm.nih.gov/34796497/" target="_blank" rel="noreferrer noopener">astringency</a>. 



The familiar sensation is therefore less about tongue chemistry than about the mechanical friction created once saliva’s slip layer has been thinned out.



<h2 class="wp-block-heading" id="h-mixtures-of-taste-and-touch">Mixtures of taste and touch</h2>



Bitterness rides a different sensory pathway, relying on taste‑bud receptors that respond to specific tannin fragments floating free in the fluid rather than to whole chains. 



Two drinks can carry the same total tannin load yet, by favoring different fragment sizes, trigger strikingly different mixtures of taste and touch.



Climate compounds the story because cooler regions produce grapes with fewer skin tannins and shorter seed tannins. As a result, wines from Pennsylvania or Scandinavia often feel lighter than peers from California or Australia even when alcohol, color, and sugar match. 



This gap has long frustrated growers who cannot simply boost tannin numbers without upsetting balance elsewhere.



<h2 class="wp-block-heading" id="h-tannin-structure-and-wine-texture-details">Tannin structure and wine texture details</h2>



Similar <a href="https://pubmed.ncbi.nlm.nih.gov/32242660/" target="_blank" rel="noreferrer noopener">in‑source fragmentation</a> approaches are gaining traction across metabolomics because they deliver tandem‑level structural detail on instruments that usually collect only parent masses, saving both money and analysis time. 



The Penn State team adapted the trick for tannins by firing three voltage steps (gentle, moderate, and high) at each molecule. This ensured that dimers, trimers, and longer polymers all leave distinctive fingerprints.



The researchers validated the workflow on 19 lab mixtures whose tannin <a href="https://www.earth.com/news/wine-production-in-a-warming-world-the-winners-and-losers/" target="_blank" rel="noreferrer noopener">recipes</a> were already known, deliberately mixing short and long chains to challenge the algorithm. 



The fingerprint report matched within two percentage points across the board, then repeated the performance on eight commercial ciders where the ingredient lists were revealed only after testing.



<h2 class="wp-block-heading" id="h-why-does-it-matter">Why does it matter?</h2>



The precision of the tannin fingerprinting method matters because classic colorimetric or precipitation assays lump every tannin together, masking the structural fine print that drives texture and health activity. 



Without that information, winemakers have been forced to tweak fermentation time, barrel choice, or fining agents by taste alone and hope the chemistry followed.



“Sometimes that tannic element is really harsh, like dragging sandpaper across your tongue. Other times it is velvety or smooth,” said Kwasniewski.&nbsp;



<h2 class="wp-block-heading" id="h-manipulating-the-texture-of-wine">Manipulating the texture of wine</h2>



Pennsylvania vintners often struggle to build the weightier mouthfeel associated with <a href="https://pfaf.org/user/Plant.aspx?LatinName=vitis+vinifera" target="_blank" rel="noreferrer noopener">Vitis vinifera</a> harvested in warmer valleys where skins thicken and seeds ripen fully. 



With the new fingerprint in hand, they can select clones, tweak maceration length, or add oak alternatives in a more targeted quest for body.



Because the read‑out comes from a one‑minute <a href="https://chem.libretexts.org/Bookshelves/Analytical_Chemistry/Supplemental_Modules_(Analytical_Chemistry)/Instrumentation_and_Analysis/Chromatography/Liquid_Chromatography" target="_blank" rel="noreferrer noopener">liquid‑chromatography</a> run, small wineries could check fermentations each morning, log the tannin profile, and steer punch‑downs or blending before irreversible changes set in. 



Kwasniewski’s group is beta‑testing a suitcase‑sized instrument that can plug into the hose manifold next to the press.



Cider makers and craft‑beer <a href="https://www.earth.com/news/red-or-white-the-surprising-truth-about-wine-and-cancer-risk/" target="_blank" rel="noreferrer noopener">brewers</a> have joined the conversation, chasing the sweet spot where bitterness perks up flavor without tipping into harsh drying. 



Early trials suggest they can tune ingredient blends to drop perceived bitterness by fifteen percent while keeping the bright snap consumers expect.



<h2 class="wp-block-heading" id="h-tannin-structure-and-health-benefits">Tannin structure and health benefits</h2>



Beyond flavor, tannin architecture parallels antioxidant power in foods such as dark chocolate, where procyanidins shoulder much of the <a href="https://www.cancer.gov/publications/dictionaries/cancer-terms/def/free-radical" target="_blank" rel="noreferrer noopener">free‑radical</a> scavenging load. 



Early <a href="https://www.sciencedirect.com/science/article/abs/pii/S0955286302002152" target="_blank" rel="noreferrer noopener">work</a> shows that lengthening certain procyanidin chains can boost oxidative‑stress protection in tissue models without altering taste.



The Penn State fingerprint could therefore let nutrition researchers screen <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC4696435/" target="_blank" rel="noreferrer noopener">cocoa</a> batches or tea harvests for the most potent molecular forms before those ingredients reach candy factories or teabags. Regulators in turn might rely on the data to validate label claims about flavanol content.



It could also clarify why some epidemiological reports tie moderate red‑<a href="https://www.earth.com/news/moderate-wine-consumption-reduces-cardiovascular-risks/" target="_blank" rel="noreferrer noopener">wine</a> intake to vascular benefits while others find weaker links. Differentiating tannin shapes instead of measuring simple totals may reconcile those mixed results and point nutrition guidelines toward structure‑specific thresholds.



<h2 class="wp-block-heading" id="h-future-uses-of-tannin-fingerprinting">Future uses of tannin fingerprinting</h2>



The team now plans to push detection toward even larger tannin polymers that dominate age‑worthy reds - a task that may require higher voltages or alternative ionization modes to break the stubborn giants apart. 



Parallel work aims to translate the approach to <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC9796155/" target="_blank" rel="noreferrer noopener">white‑wine phenolics</a>, coffee, and even hops.



Collaborations with grape breeders are under way to evaluate experimental crosses for mouthfeel before full planting, turning sensory instinct into data that farmers can act on. 



If the project succeeds, future drink labels could list nuanced tannin fingerprints alongside alcohol percentage and acidity.



The study is published in the <a href="https://pubs.acs.org/doi/10.1021/acs.jafc.5c02379?goto=supporting-info" target="_blank" rel="noreferrer noopener">Journal of Agricultural and Food Chemistry</a>.



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Hidden chemistry of wine: What actually shapes its texture?

Take a sip of cabernet and your tongue might feel...

Sea anemones look like simple, radial animals. Yet their bodies hide a front-to-back plan that mirrors the layout seen in animals with heads and tails. 



A new study shows that the cells of these soft-bodied creatures read chemical hints to decide which side becomes “back” and which becomes “belly.”



<h2 class="wp-block-heading" id="h-link-between-sea-anemones-and-humans">Link between sea anemones and humans </h2>



Scientists at the <a href="https://www.univie.ac.at/en/" target="_blank" rel="noreferrer noopener">University of Vienna</a> found that sea anemones rely on a process called BMP shuttling to organize their developing bodies. 



This same biological mechanism is responsible for shaping the body axes in many familiar animals from insects to vertebrates, including humans.



The discovery pushes the origin of this cellular traffic system back more than 600 million years, suggesting it was already present in a common ancestor of nearly all modern <a href="https://www.earth.com/news/animals-share-hidden-behavior-patterns-across-continents/" target="_blank" rel="noreferrer noopener">animals</a>.



This finding not only highlights the deep evolutionary connection between simple and complex organisms but also opens up new ways of thinking about how body plans are genetically encoded and inherited across generations. 



The research suggests that what we see in modern animals may be built upon a remarkably ancient and shared developmental toolkit.



<h2 class="wp-block-heading" id="h-signals-that-guide-developing-cells">Signals that guide developing cells</h2>



Bone Morphogenetic Proteins (BMPs) are signals that guide developing <a href="https://www.earth.com/news/how-did-the-first-cells-life-form-on-earth-scientists-think-they-finally-figured-it-out/" target="_blank" rel="noreferrer noopener">cells</a>. A partner molecule, Chordin, can both block these signals and move them to new spots.



The moving act - shuttling - creates precise highs and lows of BMP activity. Early cells read these highs and lows like a map, turning into skin, nerve tissue, or other organs.



The researchers worked with Nematostella vectensis, a small sea anemone commonly used in laboratory studies.



<h2 class="wp-block-heading" id="h-body-development-in-sea-anemones">Body development in sea anemones </h2>



To understand how Chordin functions, they first blocked its production in developing sea anemone embryos. As a result, BMP activity came to a halt, and the second body axis failed to form.



To test Chordin’s role further, the team introduced two different forms of the molecule: one that was fixed in place and could not move, and another that was free to drift through the embryo. 



Only the free-moving version was able to restore BMP signaling on the opposite side of the embryo. This result showed that Chordin does more than just block BMPs - it actively shuttles them across the developing body.



<h2 class="wp-block-heading" id="h-why-this-matters-for-evolution">Why this matters for evolution</h2>



David Mörsdorf is the first author of the study and a postdoctoral researcher in the Department of Neurosciences and Developmental Biology at the University of Vienna.



"Not all Bilateria use Chordin-mediated BMP shuttling, for example, <a href="https://www.earth.com/news/frogs-and-toads-face-new-risks-as-their-habitats-dry-up/" target="_blank" rel="noreferrer noopener">frogs</a> do, but fish don't, however, shuttling seems to pop up over and over again in very distantly related animals making it a good candidate for an ancestral patterning mechanism," said Mörsdorf.



"The fact that not only bilaterians but also sea anemones use shuttling to shape their body axes, tells us that this mechanism is incredibly ancient. It opens up exciting possibilities for rethinking how body plans evolved in early animals."



Grigory Genikhovich, senior author of the study, added that experts might never be able to exclude the possibility that bilaterians and bilaterally symmetric cnidarians evolved their bilateral <a href="https://www.earth.com/news/500-million-year-old-fish-armor-may-be-the-reason-your-teeth-hurt/" target="_blank" rel="noreferrer noopener">body plans</a> independently.



"However, if the last common ancestor of Cnidaria and Bilateria was a bilaterally symmetric animal, chances are that it used Chordin to shuttle BMPs to make its back-to-belly axis. Our new study showed that," said Genikhovich.



<h2 class="wp-block-heading" id="h-future-clues-in-simpler-creatures">Future clues in simpler creatures</h2>



The work suggests that a single, ancient blueprint guided the rise of complex body shapes across many animal lineages. Future studies may search for BMP shuttling in even older or simpler groups, testing just how deep this shared strategy runs in the history of life.



Understanding BMP shuttling in sea anemones doesn’t just tell us about the past - it could also shape the future. 



Because BMP signals are important in how all kinds of animals develop their bodies, including humans, this research could help scientists better understand <a href="https://www.earth.com/news/dog-nose-shapes-could-help-explain-human-birth-defects/" target="_blank" rel="noreferrer noopener">birth defects</a>, tissue growth, and even how to guide stem cells into becoming the right types of tissue.



By studying these simple creatures, researchers may unlock clues about how to repair or regrow parts of the human body. And by tracing the history of how body plans evolved, scientists can more confidently predict which genes or molecules are truly essential across all animal life.



The full study was published in the journal <a href="https://www.science.org/doi/10.1126/sciadv.adu6347" target="_blank" rel="noreferrer noopener">Science Advances</a>.



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Sea anemones share a biological trick with humans

Sea anemones look like simple, radial animals. Yet their bodies...

Down syndrome is caused by an extra copy of chromosome 21, which leads to a range of developmental differences. Researchers have long sought strategies to correct this duplication, because current interventions do not address the added genetic material at its source.



Recent work points to a promising approach with <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC7508700/" target="_blank" rel="noreferrer noopener">CRISPR-based methods</a>. 



<a href="https://www.researchgate.net/profile/Ryotaro-Hashizume-2" target="_blank" rel="noreferrer noopener">Ryotaro Hashizume</a> and colleagues from <a href="https://www.mie-u.ac.jp/en/R-navi/" target="_blank" rel="noreferrer noopener">Mie University</a> in Japan report that it is possible to cut away the surplus chromosome in affected cells, which appears to bring their behavior closer to typical function.



<h2 class="wp-block-heading" id="h-why-an-extra-chromosome-matters">Why an extra chromosome matters</h2>



<a href="https://www.cdc.gov/ncbddd/birthdefects/downsyndrome.html" target="_blank" rel="noreferrer noopener">Down syndrome</a> affects about 1 in 700 newborns in the United States. That added chromosome, known as <a href="https://www.chop.edu/conditions-diseases/trisomy-21-down-syndrome" target="_blank" rel="noreferrer noopener">trisomy 21</a>, disrupts a range of important processes in the body, often resulting in learning difficulties, distinctive physical traits, and certain health concerns.



This additional genetic copy raises gene activity above normal levels. It pushes <a href="https://www.earth.com/news/scientists-discover-hidden-stem-cells-that-could-reactivate-hair-growth/">cells</a> to overwork, because they carry extra material that shifts how genes are used and how proteins are made.



<h2 class="wp-block-heading" id="h-crispr-and-down-syndrome">CRISPR and Down syndrome</h2>



<a href="https://pubmed.ncbi.nlm.nih.gov/36171658/" target="_blank" rel="noreferrer noopener">CRISPR-Cas9</a> is a versatile gene-editing system that relies on an enzyme to recognize specific DNA sequences. Once the enzyme locates a matching site, it snips through the DNA strands.



Scientists carefully design CRISPR guides to target only the unwanted chromosome. This trick is called <a href="https://www.science.org/doi/10.1126/science.1225829" target="_blank" rel="noreferrer noopener">allele-specific editing</a>, and it helps steer the cutting enzyme to the right spot.



“Trisomic rescue via allele-specific multiple chromosome cleavage using CRISPR-Cas9 in trisomy 21 cells,” wrote Hashizume. 



Their group discovered that removing the unneeded copy often normalized gene expression in laboratory-grown cells.



The treated <a href="https://www.earth.com/news/cell-division-discovery-challenges-a-century-of-textbook-biology/">cells</a> reverted to typical patterns of protein manufacturing. They also showed better survival rates in certain tests, indicating that the excess genetic burden was successfully relieved.



<h2 class="wp-block-heading" id="h-potential-for-neurons-and-beyond">Potential for neurons and beyond</h2>



The technique is still far from clinical use, so it will not show up in routine care anytime soon. However, scientists are considering whether similar edits might be done in cells that form the brain and other tissues.



The possibility of trimming excess genetic material in <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC3070107/" target="_blank" rel="noreferrer noopener">nondividing cells</a> is also intriguing. 



Many cells in the body do not actively divide after maturing, yet the team’s findings suggest that these cells could still benefit from targeted chromosome removal.



<h2 class="wp-block-heading" id="h-karyotype-and-brain-related-genes">Karyotype and brain-related genes</h2>



In follow-up tests, researchers examined how gene activity changed after removing the extra chromosome. 



They noticed that genes tied to nervous system development became more active, while those linked to metabolism were dialed down.



This shift in gene expression could help explain how correcting the chromosomal imbalance affects the cell’s overall behavior. It also supports earlier <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC3273608/" target="_blank" rel="noreferrer noopener">findings</a> that extra copies of chromosome 21 disrupt brain development during early fetal growth.



<h2 class="wp-block-heading" id="h-tested-in-both-stem-and-skin-cells">Tested in both stem and skin cells</h2>



The researchers didn’t just test their approach on lab-grown stem cells. They also applied it to <a href="https://www.sciencedirect.com/topics/medicine-and-dentistry/skin-fibroblast" target="_blank" rel="noreferrer noopener">skin fibroblasts</a>, which are more mature, non-stem cells taken from people with Down syndrome.



Even in these fully developed cells, the method successfully removed the extra chromosome in a significant number of cases. 



That result hints at broader possibilities for correcting the genetic issue in different cell types throughout the body.



<h2 class="wp-block-heading" id="h-removal-improved-cell-health">Removal improved cell health</h2>



After removing the extra chromosome, the corrected cells grew slightly faster and had a shorter doubling time compared to untreated trisomy cells. 



These changes suggest that getting rid of the surplus chromosome may ease the biological stress that slows down cell growth.



The corrected cells also produced fewer <a href="https://www.cancer.gov/publications/dictionaries/cancer-terms/def/reactive-oxygen-species" target="_blank" rel="noreferrer noopener">reactive oxygen species</a>, which are harmful byproducts linked to cell damage and aging. 



Lower levels of these molecules point to improved mitochondrial function and a general boost in cell fitness.



Some of the CRISPR cuts can affect healthy chromosomes. The researchers are addressing this by refining their guidance molecules, so they only latch onto the extra <a href="https://medlineplus.gov/genetics/chromosome/21/" target="_blank" rel="noreferrer noopener">chromosome 21</a>.



They are also investigating ways to keep the cell’s repair systems from reversing or botching the intended edits. With more work, the method might become safer and more efficient for a wide range of tissues.



<h2 class="wp-block-heading" id="h-implications-for-future-treatments">Implications for future treatments</h2>



If scientists confirm these early results in additional studies, they might one day design therapies that quiet the <a href="https://www.earth.com/news/scientists-decipher-the-genetic-history-of-400-medieval-skeletons/">genetic</a> overload at its source. This approach could apply to lab-grown tissues or stem <a href="https://www.earth.com/news/how-plants-build-their-cell-walls-is-seen-by-scientists-for-the-first-time-ever/">cells</a> aimed at regenerative treatments.



Experts emphasize that these findings do not guarantee a straightforward path to therapy. Still, the work highlights how CRISPR could assist in handling fundamental genetic hiccups that cause common conditions.



The project shows that CRISPR can remove an entire chromosome rather than making small fixes. That is a big jump in what genome editing can accomplish.



Researchers will likely continue analyzing the risks of widespread <a href="https://www.earth.com/news/dna-from-9000-year-old-skeletons-disproves-migratory-waves-theory-from-south-africa/">DNA</a> changes. They will also check how these modified cells behave over longer periods and whether they stay healthy in real-world settings.



The study is published in <a href="https://academic.oup.com/pnasnexus/article/4/2/pgaf022/8016019?login=false" target="_blank" rel="noreferrer noopener">PNAS Nexus</a>.



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CRISPR used to remove extra chromosomes in Down syndrome and restore cell function

Down syndrome is caused by an extra copy of chromosome...

Fungi,Aspergillus,,Black,Mold,,Which,Produce,Aflatoxins,And,Cause,Pulmonary

Imagine inhaling hundreds of invisible spores every day. Most float in and out without leaving a trace. Yet some belong molds that don't respect boundaries.



Some fungus species will infect lungs, spoil crops, and disrupt ecosystems all at the same time. In short, they can wreak massive havoc and leave death in their wake.



Most molds and fungi are helpful, but some fungus and mold will jump from hospital wards to honeybee hives, and the line between helpful recycler and harmful invader grows blurrier each year.



Most of the time, healthy immune systems swat away dangerous spores and fight off infection. Trouble arises when weakened defenses, rising temperatures, and heavy fungicide use tip the scales. 



Suddenly, the same fungus that quietly decomposes the fallen leaves in your yard can trigger relentless coughs, damage corn silos, and shrug off medicines that once kept it in check.



<h2 class="wp-block-heading" id="h-aspergillus-fungus-easily-adapts">Aspergillus fungus easily adapts</h2>



After studying fungal threats for years, Dr. Norman van Rhijn and colleagues at <a href="https://www.manchester.ac.uk/" target="_blank" rel="noreferrer noopener">The University of Manchester</a> mapped how three notorious Aspergillus species - A. flavus, A. fumigatus, and A. niger - might spread through the end of the century. 



They fed climate change scenarios into global models and watched the virtual spores drift. One scenario (SSP585), which assumes a fossil-fuel-dependent future, paints an unsettling picture: habitats across Europe become markedly friendlier to these pathogens.



Aspergillus fungus thrives because its genome bends easily to new pressures. It lives on soil, grains, animal feathers, even coral skeletons. Out in the wild, it recycles nutrients, but on farms and in clinics, the story shifts. 



Farmers spray <a href="https://www.earth.com/news/super-fungus-is-among-us-drug-resistant-fungi-is-thriving-in-every-corner-of-the-earth/" target="_blank" rel="noreferrer noopener">azole fungicides</a> to protect wheat and peanuts; doctors use nearly identical azole drugs to save patients with lung infections. That overlap nudges Aspergillus toward drug resistance - similar to bacteria evolving against <a href="https://www.earth.com/news/earth-rivers-are-highly-saturated-with-human-antibiotics-helping-bacteria-develop-resistance/" target="_blank" rel="noreferrer noopener">antibiotics</a>.



<h2 class="wp-block-heading" id="h-climate-reshapes-global-mold-map">Climate reshapes global mold map</h2>



Temperature, humidity, and extreme weather events dictate where spores settle. 



“Changes in environmental factors, such as humidity and extreme weather events, will change habitats and drive fungal adaptation and spread,” said Dr. van Rhijn. 



“We’ve already seen the emergence of the fungus <a href="https://www.earth.com/news/toxic-microbes-aerosols-can-travel-thousands-of-miles-through-the-air/" target="_blank" rel="noreferrer noopener">Candida auris</a> due to rising temperatures, but, until now, we had little information on how other fungi might respond to this change in the environment.” 



He added that fungi remain “relatively under-researched compared to viruses and parasites,” yet the new maps show they will likely reach “most areas of the world in the future.”



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/06/Aspergillus_global-distributions_map_credit-MaxENT_1m.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/06/Aspergillus_global-distributions_map_credit-MaxENT_1s.webp" alt="MaxENT model accurate described Aspergillus global distributions. Credit: University of Manchester" class="wp-image-1973600"/></a><figcaption class="wp-element-caption">MaxENT model accurate described Aspergillus global distributions. Click image to enlarge. Credit: University of Manchester</figcaption></figure>



Those maps point to striking numbers. Under the high-emissions pathway, the range of A. flavus in Europe could jump about 16 percent, potentially putting another one million people at risk of infection. 



A. fumigatus - the chief culprit behind invasive aspergillosis - could expand its European footprint by 77.5 percent, threatening up to nine million more residents. 



In Africa, paradoxically, parts of the continent may become too hot for some fungi to survive, hinting at complex regional trade-offs.



<h2 class="wp-block-heading" id="h-forecasting-aspergillus-fungus-spread">Forecasting Aspergillus fungus spread</h2>



Forecasting pathogens decades ahead may sound speculative, but it builds on earlier warnings. Hospitals already grapple with Aspergillus fungus outbreaks after building renovations or severe dust storms. 



Meanwhile, intensive-care units report stubborn cases in patients recovering from influenza or COVID-19. 



Rising outdoor spore loads could translate to more <a href="https://www.earth.com/news/how-do-deadly-molds-attack-the-immune-system-of-humans/" target="_blank" rel="noreferrer noopener">hospital admissions</a> and costlier treatments, especially because diagnostics for fungal infections lag far behind those for bacteria or viruses.



Mycotoxin contamination adds another layer. A single year of heavy Aspergillus growth can saddle the U.S. corn industry with losses topping $1 billion. 



Increased heat and humidity extend the window for mold growth in silos and fields, forcing farmers to discard grain or blend batches to dilute toxins - strategies that still carry economic and health risks.



<h2 class="wp-block-heading" id="h-current-drugs-don-t-work">Current drugs don't work</h2>



Azole resistance has climbed steadily in Europe and Asia. Patients with resistant Aspergillus fungus infections face mortality rates exceeding 50 percent, partly because alternative drugs can damage the kidneys or liver. 



Each hectare treated with agricultural azoles raises the odds that environmental spores will carry resistance genes into hospitals. 



Public-health agencies now track these genes in soil and compost piles, hoping to spot trouble before it reaches intensive care.



Fungicide demand is also changing. As some African regions exceed the thermal limits for certain molds, farmers elsewhere may spray more to protect lengthening growing seasons.



That feedback loop - more fungicide, <a href="https://www.earth.com/news/soil-plays-an-overlooked-role-in-antibiotic-resistance/" target="_blank" rel="noreferrer noopener">stronger resistance</a> - complicates food security and patient care alike.



<h2 class="wp-block-heading" id="h-farms-food-and-rising-bills">Farms, food, and rising bills</h2>



Aspergillus isn’t the lone shapeshifter. Fusarium, which devastates wheat and oat fields, and Cryptococcus, an opportunistic pathogen in AIDS patients, also respond to warming climates. 



“Fungal pathogens pose a serious threat to human health by causing infections and disrupting food systems. Climate change will make these risks worse," explains Viv Goosens of <a href="https://wellcome.org/" target="_blank" rel="noreferrer noopener">Wellcome</a>.



"To address these challenges, we must fill important research gaps. By using models and maps to track the spread of fungi, we can better direct resources and prepare for the future.”



<h2 class="wp-block-heading" id="h-aspergillus-fungus-and-human-health">Aspergillus fungus and human health</h2>



Fungi account for an estimated 1.5 to 3.8 million species, yet fewer than 10 percent carry official descriptions, and only a sliver have sequenced genomes. 



The scarcity of basic data hinders vaccine development and slows the hunt for safer drug targets. 



Recognizing this blind spot, the <a href="https://www.who.int" target="_blank" rel="noreferrer noopener">World Health Organization</a> added Aspergillus fungus and Candida species to its priority list for emerging threats in 2022.



Researchers now call for <a href="https://www.earth.com/news/future-of-food-safety-ai-can-detect-contamination-early/" target="_blank" rel="noreferrer noopener">coordinated monitoring</a> - combining air quality sensors, agricultural sampling, and hospital surveillance - to trace spore movement in near-real time. 



Such efforts could flag hotspots, guide fungicide regulations, and spark investment in rapid diagnostics. Without them, today’s manageable mold may evolve into tomorrow’s silent pandemic.



No single fix will erase the risk. Cutting greenhouse gas emissions limits the environmental changes that favor Aspergillus fungus. 



Smarter fungicide policies slow resistance on farms. Better ventilation in buildings reduces indoor spore counts, while new antifungal classes extend doctors’ toolkits. 



Piece by piece, these steps can keep an ancient decomposer from becoming an outsized menace in a warming world.



The full study was published in the journal <a href="https://www.researchsquare.com/article/rs-6545782/v1" target="_blank" rel="noreferrer noopener">Research Square</a>.



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Deadly fungus that can "eat you from the inside out" is quickly spreading around the world

Imagine inhaling hundreds of invisible spores every day. Most float...

Mammoth Cave in Kentucky stretches for more than 420 miles (675 kilometers) below the surface of the ground and is often described as the world’s largest cave system. Recent explorations there uncovered two new fossil sharks that once roamed shallow coastal waters more than 325 million years ago.



Ancient shark specialist John-Paul (JP) Hodnett of the Maryland-National Capital Parks and Planning Commission (<a href="https://www.mncppc.org/" target="_blank" rel="noreferrer noopener">MNCPPC</a>) worked with the <a href="https://www.nps.gov/subjects/fossils/index.htm">National Park Service Paleontology Program</a> to identify the fossils. 



These finds have everyone buzzing because they offer a glimpse into marine habitats that thrived when parts of what is now eastern North America were covered by a warm sea.



<h2 class="wp-block-heading" id="h-prehistoric-shark-fossil-puzzle">Prehistoric shark fossil puzzle</h2>



The newly documented sharks are Troglocladodus trimblei and Glikmanius careforum, and they are from a group known as <a href="https://www.uky.edu/KGS/fossils/fossil-month-cten.php">ctenacanth</a> sharks. 



They both measured about 10–12 feet (3–3.6 meters) long, which is similar in size to an oceanic whitetip shark.



The shark fossils were collected from various limestone formations, which were deposited during the Middle to Late <a href="https://www.nps.gov/articles/000/mississippian-period.htm">Mississippian Period</a>. 



The bigger picture is that these habitats were once submerged under shallow seas and supported a wide range of fish life. Researchers have now identified more than 70 ancient fish species in the cave system.



A partial set of jaws belonging to a young <a href="https://shark-references.com/species/view/Glikmanius-careforum">Glikmanius careforum</a> revealed fresh details about cartilage, which rarely fossilizes well. 



Cartilaginous remains of sharks are often fragile and easily destroyed by erosion, so finding them preserved in a protected space is especially rewarding.



Experts note that this newly identified material adds depth to ongoing discussions of how shark groups diversified while the supercontinent <a href="https://www.usgs.gov/faqs/what-was-pangea">Pangea</a> was taking shape.



<h2 class="wp-block-heading" id="h-collaborations-and-fieldwork">Collaborations and fieldwork</h2>



“Every new discovery at Mammoth Cave is possible due to collaborations,” said park superintendent <a href="https://www.nps.gov/maca/learn/management/index.htm">Barclay Trimble</a> of Mammoth Cave National Park. 



Researchers and volunteers have explored hidden passages, river channels, and even narrow crawlways in search of key fossils.



Members of the <a href="https://www.cave-research.org/" target="_blank" rel="noreferrer noopener">Cave Research Foundation</a> also took part in these efforts. The name Glikmanius careforum was chosen to honor that organization’s valuable support in the field.



The partial cartilage from this genus points to a short head with a strong bite, possibly used to feed on smaller fish and <a href="https://www.geo.mtu.edu/KeweenawGeoheritage/HoughtonEC/Orthocones.html">orthocones</a>, which are squid-like creatures with elongated shells.



<h2 class="wp-block-heading" id="h-fossils-help-trace-evolutionary-change">Fossils help trace evolutionary change </h2>



Troglocladodus trimblei stands out for its branching tooth design that helped it secure prey in the Mississippian seas. 



This prehistoric hunter probably shared a coastal environment with G. careforum, in waters that covered modern-day Kentucky and Alabama.



Researchers say these sharks likely thrived in nearshore habitats that teemed with bony fish, shelled organisms, and other <a href="https://www.earth.com/news/cocaine-sharks-brazilian-waters-sharpnose-sharks-rhizoprionodon-lalandii-ocean-pollution/">marine creatures</a>.



Tracing these fossils across multiple rock layers provides insights into how the environment changed over time. 



Coastal waters rose and fell as landmasses drifted toward each other, gradually merging into a single continent. 



These broader patterns helped shape the distribution and evolutionary paths of ancient sharks like T. trimblei and G. careforum.



<h2 class="wp-block-heading" id="h-how-to-preserve-shark-fossils">How to preserve shark fossils</h2>



Field teams spent long hours underground carefully mapping and collecting small fragments of teeth. A single <a href="https://www.npca.org/articles/7703-the-unveiling-of-mammoth-cave-s-history">tooth</a> from T. trimblei sparked initial interest when Superintendent Trimble first discovered it on a 2019 trip. 



Seasoned cavers and geologists coordinated to ensure safe retrieval of each piece, knowing that one misstep could damage the delicate remains.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/06/ctenacanth-sharks_cave-discovery_325-million-years-ago_1big.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/06/ctenacanth-sharks_cave-discovery_325-million-years-ago_1s.webp" alt="A reconstruction of the new Middle to Late Mississippian ctenacanth sharks from Mammoth Cave National Park and northern Alabama. Glikmanius careforum is seen swimming in the foreground with two Troglocladodus trimblei swimming above. Artwork by Benji Paynose" class="wp-image-1973763"/></a><figcaption class="wp-element-caption">A reconstruction of the new Middle to Late Mississippian ctenacanth sharks from Mammoth Cave National Park and northern Alabama. Glikmanius careforum is seen swimming in the foreground with two Troglocladodus trimblei swimming above. Click image to enlarge. Artwork by Benji Paynose</figcaption></figure>



Research at Mammoth Cave has led to conversations about how best to preserve fragile fossils within difficult-to-access passages. Experts say stable cave temperatures help keep these discoveries in good condition. 



Park managers have also integrated these new data into guidelines for future research so that more clues to marine life from 325 million years ago may be found.



<h2 class="wp-block-heading" id="h-why-these-shark-fossils-matter">Why these shark fossils matter</h2>



Scientists use these finds to compare local fossil collections with specimens from similar periods in other parts of the world. 



Documenting body sizes, tooth arrangements, and skeletal details helps researchers build a clearer timeline of shark <a href="https://www.earth.com/news/shark-skeletons-could-lead-to-technological-innovations/">evolution</a>.



These comprehensive studies uncover shifts in fish diversity that occurred as oceans changed and landmasses joined together. 



Experts also link fossil data with knowledge from bony fish records, coral structures, and other sea life. This combined approach paints a full picture of ancient marine habitats and shows how some species adapted while others vanished. 



The two new fossil sharks at Mammoth Cave highlight that even well-known geologic areas can hold <a href="https://www.earth.com/news/octopus-caught-riding-on-the-back-of-the-worlds-fastest-shark-in-the-open-ocean/">surprises</a> for many years.



<h2 class="wp-block-heading" id="h-future-cave-explorations">Future cave explorations</h2>



Mammoth Cave continues to yield glimpses into a vanished coastline that spanned what is now Kentucky, Europe, and northern Africa. 



T. trimblei and G. careforum are just two recent additions to an ever-expanding fossil catalog, reminding everyone that exploration still brings answers and new questions.



In many ways, these ancient sharks highlight how puzzle pieces of geologic history keep fitting together. Field teams are now eager to see what lies in deeper chambers or behind the narrow channels.



The next phase of study may involve more advanced imaging and careful excavation in lesser-known passages, guided by new mapping techniques. 



Findings like these spur a broader appreciation for the cave system’s scientific value, well beyond its length or visual features.



The study is published in the <a href="https://www.researchgate.net/publication/377873693_NEW_CTENACANTH_SHARKS_CHONDRICHTHYES_ELASMOBRANCHII_CTENACANTHIFORMES_FROM_THE_MIDDLE_TO_LATE_MISSISSIPPIAN_OF_KENTUCKY_AND_ALABAMA">Journal of Vertebrate Paleontology</a>.



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Two prehistoric sea monsters found after 325 million years in the world’s largest cave

Mammoth Cave in Kentucky stretches for more than 420 miles...

The subtropical jet stream - a fast-moving air current high above the Earth - is behind a dramatic drop in primary production in the northwestern Mediterranean.



According to a recent study, the drop in productivity is linked to a gradual northward shift in this high-altitude wind belt, which regulates weather and drives the upwelling of nutrient-rich water.



The research was conducted by experts at the <a href="https://web.ub.edu/web/ub/" target="_blank" rel="noreferrer noopener">University of Barcelona</a> and the Institute of Marine Sciences (ICM-CSIC). 



The team paired satellite data on ocean color with atmospheric observations. The analysis revealed that a subtle change in <a href="https://www.earth.com/news/the-westerly-winds-are-changing-and-the-consequences-are-unknown/" target="_blank" rel="noreferrer noopener">wind patterns</a> can ripple through the water column and reshape an ecosystem.



<h2 class="wp-block-heading" id="h-a-jet-stream-on-the-move">A jet stream on the move</h2>



The surface atmospheric circulation and associated marine dynamics are the processes most affected by the northward displacement of the jet stream, noted study co-author Professor Miquel Canals. 



"Northerly winds drive the upwelling of nutrient-rich deep waters, so the alteration of their behavior has considerably weakened the intensity of this upwelling and, therefore, has reduced the supply of nutrients to the sea surface," explained Professor Canals. 



“Deep water reaching the ocean surface is essential to nourish <a href="https://www.earth.com/news/tiny-phytoplankton-that-feed-ocean-life-are-rapidly-disappearing/" target="_blank" rel="noreferrer noopener">phytoplankton</a>, which is the basis of the marine food web. Consequently, the weakening of upwelling at the regional level has directly impacted marine primary production, causing a decline of up to 40% in just over two decades."



When those winds weaken, the supply of nutrients from the deep slows down - a change that hits phytoplankton hardest. The entire food web, from tiny <a href="https://www.earth.com/news/zooplankton-are-rapidly-escalating-the-threat-of-nanoplastics/" target="_blank" rel="noreferrer noopener">zooplankton</a> to commercially valuable fish, feels the squeeze.



<h2 class="wp-block-heading" id="h-jet-stream-changes-and-marine-life">Jet stream changes and marine life</h2>



Earlier studies hinted at falling productivity in parts of the Spanish Mediterranean. Julia Crespín, first author of the current study, noted that the previous research confirmed similar losses - but not related to the phenomenon of jet currents. She added that the broader literature is mixed. 



“Apart from that, several studies deal with the relationship between <a href="https://www.earth.com/news/climate-change-will-accelerate-jet-stream-winds-and-airplane-turbulence/" target="_blank" rel="noreferrer noopener">climate change</a> and marine primary production with contradictory results: while some point to a decrease in primary production, others indicate an increase,” said Crespin.



The new work links the dots by focusing on the jet stream’s drift - a trend also seen in other climate records.



<h2 class="wp-block-heading" id="h-tracking-wind-water-and-life">Tracking wind, water, and life</h2>



To tease out the link between a drifting jet stream and marine life, the researchers tracked four key variables. According to study co-author Jordi Solé, these variables included the position of the jet stream in the study area and the Ekman transport - a wind-induced movement of water mass towards the surface.



The team also tracked northerly wind stress on the sea surface, which is a determining factor for the formation of <a href="https://www.earth.com/news/tropical-winds-support-the-worlds-most-productive-ocean-systems/" target="_blank" rel="noreferrer noopener">upwelling</a> in the study area, and the depth-integrated chlorophyll concentration.



Chlorophyll levels in the water serve as an indicator of phytoplankton abundance, and therefore reflect marine primary production.



"With these variables, we have established relationships between changes in the atmosphere and the biological response of the surface ocean, which has helped us to better understand how the jet stream ultimately affects marine primary production," said Solé.



<h2 class="wp-block-heading" id="h-the-cost-of-a-moving-jet-stream">The cost of a moving jet stream</h2>



Less phytoplankton means the ocean absorbs less carbon dioxide, so the atmospheric budget worsens. Fisheries may also struggle as lower rations at the base of the web work their way up the chain.



“Our study provides a new perspective by showing that, at least in the northwestern Mediterranean, the northward shift of the jet stream is weakening the mechanisms and interactions that drive upwelling, which has contributed to a significant decline in marine primary production," explained the researchers.



“We consider that the change in the wind pattern is the factor that conditions the behavior of the ecosystem, beyond dichotomies about its intensification or the effect of temperature." 



"Thus, we point to a totally new factor that focuses especially on the dynamic behavior of both the atmosphere and the ocean (and their interaction) as the key to understanding its future evolution."



<h2 class="wp-block-heading" id="h-looking-beyond-the-mediterranean">Looking beyond the Mediterranean</h2>



The Mediterranean is a semi-enclosed basin with unique winds and currents, so the team cautions against a one-size-fits-all conclusion. Still, the jet stream is drifting in many regions, and similar studies may reveal comparable effects on marine life elsewhere.



The researchers emphasized that today’s tools - from satellites to high-resolution climate models - are finally catching up with the complexity of ocean-atmosphere systems.



“Never before has there been as much data as there is today, or as powerful tools to manage, analyze and interpret it as there are today." 



"In this context, it is crucial to continue research in this line of work, combining data from in situ observation, from remote sensors such as those installed on satellites, and from high-resolution climate models to better understand the physical and biological mechanisms involved, the interactions created, the interannual variability and the potential effects they generate."



The experts also noted that these interactions may not be constant year-to-year, and their global relevance is still unfolding.



“It will also be necessary to further study interannual variability and the mechanisms that explain why this connection is stronger in some years than in others, as well as to explore how such changes may affect other marine regions around the world," the researchers concluded. 



"We understand this is a line of work that promises major advances in the coming years."



The full study was published in the journal <a href="https://www.sciencedirect.com/science/article/pii/S0079661125000825?via%3Dihub" target="_blank" rel="noreferrer noopener">Progress In Oceanography</a>.



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How a wandering jet stream is draining marine life in the Mediterranean Sea

The subtropical jet stream - a fast-moving air current high...

It can be challenging to spot the everyday forces that keep our ocean in harmony. We often think of sunlight, waves, and tides as the main players in our seas, but there is more to the story.



A new study shows that <a href="https://oceanservice.noaa.gov/facts/marinesnow.html" target="_blank" rel="noreferrer noopener">marine snow</a> (tiny bits of drifting debris) acts as a hotspot for bacteria that help maintain key processes in the water.



These unexpected helpers turn inert nitrogen gas into a form that organisms can use, a process called <a href="https://overton.tamu.edu/faculty-staff/gerald-wayne-evers/cool-season-legumes/nitrogen-fixation/" target="_blank" rel="noreferrer noopener">nitrogen fixation</a>. 



<a href="https://scholar.google.dk/citations?user=1FoVHbkAAAAJ&amp;hl=en" target="_blank" rel="noreferrer noopener">Subhendu Chakraborty</a> led this study at the <a href="https://www.leibniz-zmt.de/en/marine-tropics-research.html" target="_blank" rel="noreferrer noopener">Leibniz Centre for Tropical Marine Research</a> in Germany.



<h2 class="wp-block-heading" id="h-hidden-pockets-of-marine-life">Hidden pockets of marine life</h2>



Ocean waters might appear uniform at a glance. In reality, floating clumps of matter create unique zones where microbes gather. 



This <a href="https://oceanservice.noaa.gov/facts/flotsam-jetsam.html" target="_blank" rel="noreferrer noopener">flotsam</a> offers <a href="https://www.sciencedirect.com/topics/immunology-and-microbiology/heterotroph" target="_blank" rel="noreferrer noopener">heterotrophic bacteria</a> the right mix of low-oxygen centers and enough organic bits to keep them going.



Researchers tapped into mathematical models to find out how these bacteria manage to fix nitrogen across different latitudes. 



By simulating conditions from warmer tropical regions to colder areas, they noted that these <a href="https://www.earth.com/news/some-bacteria-breathe-by-creating-electricity/">bacterial</a> communities can function in waters often thought to be beyond their comfort zone.



<h2 class="wp-block-heading" id="h-why-nitrogen-matters-to-bacteria">Why nitrogen matters to bacteria</h2>



Every living thing needs nitrogen to build proteins and other vital molecules. In many parts of the ocean, dissolved nitrogen gas is abundant, but most organisms cannot use it in that form. 



Some ocean <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC10456358/" target="_blank" rel="noreferrer noopener">cyanobacteria</a> can work this gas into a usable state in sunlit waters.



Heterotrophic bacteria on particles go further by handling this job in deeper zones. They also cover a range of temperatures and oxygen levels, adding to the ocean’s overall stability. 



The scientists estimated that these particle-attached microbes contribute about 10% of total nitrogen fixation in the seas.



<h2 class="wp-block-heading" id="h-shaping-bacterial-nitrogen-fixation">Shaping bacterial nitrogen fixation</h2>



“It has been almost five years since we started this work when I was a postdoc at the <a href="https://www.ku.dk/en" target="_blank" rel="noreferrer noopener">University of Copenhagen</a>. But it was definitely worth the effort, since the results are quite a breakthrough,” explained Chakraborty. 



The discovery clears up questions about the reach of these microscopic workers.



“The magnitude of the N2 fixation and the distinct distribution of the particle-associated activity relative to what is known for cyanobacteria are highly interesting,” said <a href="https://researchprofiles.ku.dk/en/persons/lasse-riemann" target="_blank" rel="noreferrer noopener">Professor Lasse Riemann</a>, co-author of the study. 



This finding suggests a shift in how we understand productivity in ocean depths, as these bacteria are a steady support rather than mere bit players.



Temperature plays a key role in how efficiently these bacteria can fix nitrogen. The researchers discovered that fixation rates peak around 63°F (17°C) and slow down when waters get either too cold or too warm. 



At lower temperatures, <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC413996/pdf/bactrev00055-0061.pdf" target="_blank" rel="noreferrer noopener">bacterial respiration</a> slows down too much to remove oxygen from inside the particle, blocking nitrogen fixation.



At higher temperatures, the bacteria break down organic materials too quickly, which causes a mismatch. They can’t absorb the nutrients fast enough before they diffuse away. This leads to energy shortages that shut down the fixation process, even when other conditions are favorable.



<h2 class="wp-block-heading" id="h-paths-through-shifting-waters">Paths through shifting waters</h2>



Global warming raises concerns about changes in ocean chemistry. Warmer surface waters can affect where nutrients move and may reduce mixing in some areas. 



When that happens, deeper parts of the ocean could see a drop in organic matter.



Despite those challenges, results hint that these bacterial fixers might adapt well, even in cooler waters. 



That is partly because anoxic zones form in the core of large particles, giving <a href="https://www.earth.com/news/mysterious-bacteria-found-on-chinese-space-station-has-never-been-seen-before/">bacteria</a> a safe place to fix nitrogen. Some ocean regions also have extended layers of low oxygen, which can broaden their habitat.



<h2 class="wp-block-heading" id="h-wider-connections-to-marine-systems">Wider connections to marine systems</h2>



Marine biology is all about balance. <a href="https://oceanservice.noaa.gov/facts/phyto.html" target="_blank" rel="noreferrer noopener">Phytoplankton</a> often rely on fixed nitrogen, thriving when conditions are right. Fish and other sea life benefit from that growth. 



By shoring up nitrogen supplies from deeper waters, these particle-based bacteria bridge two layers of the food web.



These findings may encourage researchers to look more closely at a variety of ocean particles, including those near <a href="https://oceanexplorer.noaa.gov/facts/omz.html" target="_blank" rel="noreferrer noopener">oxygen minimum zones (OMZs)</a>. 



Learning more about how these bacterial groups live can offer guidance for long-term predictions and climate models.



<h2 class="wp-block-heading" id="h-how-oxygen-minimum-zones-boost-bacterial-activity">How oxygen minimum zones boost bacterial activity</h2>



OMZs create ideal conditions for particle-associated bacteria. These deep stretches of water, where oxygen is nearly gone, make it easier for bacteria to carry out nitrogen fixation without spending extra energy to shield their enzymes from oxygen exposure.



The study found that some of the highest nitrogen fixation rates occur within these OMZs, especially in regions like the eastern tropical Pacific and Arabian Sea. 



These zones extend over large depths, allowing for more time and space for <a href="https://www.earth.com/news/how-gut-bacteria-morganella-morganii-could-cause-depression-not-a-brain-disorder/">bacteria</a> to thrive on sinking particles rich in organic material.



<h2 class="wp-block-heading" id="h-implications-for-future-studies">Implications for future studies</h2>



Ocean dynamics are always in flux. Each year, new data shapes our approach to climate science and marine ecology. 



The recent focus on deeper-living bacteria opens fresh angles for exploring how carbon is locked away in ocean depths.



Investigations may also delve into the interplay between these heterotrophic communities and better-known nitrogen fixers. 



While cyanobacteria still rule the sunlit zones, the synergy with these newly highlighted partners underscores the intricate relationships we are only beginning to understand.



The study is published in <a href="https://www.science.org/doi/10.1126/sciadv.adq4693" target="_blank" rel="noreferrer noopener">Science Advances</a>.



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Study discovers that 'marine snow' keeps the ocean alive

It can be challenging to spot the everyday forces that...

Skipping a meal can feel like an open invitation to raid the fridge later. Scientists have long suspected that memory influences those cravings, but the brain circuitry behind it remained a mystery.



Scott Kanoski from <a href="https://dornsife.usc.edu/" target="_blank" rel="noreferrer noopener">USC Dornsife</a> and his colleagues now say they have cracked part of the code. Their latest study, which was focused on rats, identifies neurons that save a “<a href="https://www.earth.com/news/when-bacteria-get-hungry-they-turn-on-each-other/" target="_blank" rel="noreferrer noopener">meal</a> memory,” recording both what was eaten and when.



<h2 class="wp-block-heading" id="h-why-the-brain-remembers-meals">Why the brain remembers meals</h2>



Each eating episode imprints a specialized <a href="https://arxiv.org/html/2506.01659v1" target="_blank" rel="noreferrer noopener">engram</a>, a physical trace of memory that carries sensory and temporal details. 



When the team monitored rodents, cells in the <a href="https://www.sciencedirect.com/topics/medicine-and-dentistry/ventral-hippocampus" target="_blank" rel="noreferrer noopener">ventral hippocampus</a> lit up between bites, not during chewing, hinting that quiet pauses are prime time for filing the experience.



“These meal engrams function like sophisticated biological databases,” said Kanoski, the study’s senior author. He explains that location, flavor, and time stamp are <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC3607652/" target="_blank" rel="noreferrer noopener">bundled together</a> in that brief neural flash.



Human data back up the idea. Remembering a recent <a href="https://www.earth.com/news/world-food-day-fighting-global-hunger/" target="_blank" rel="noreferrer noopener">lunch</a> can trim afternoon snack intake by as much as 30 percent.



<h2 class="wp-block-heading" id="h-how-meal-memories-form">How meal memories form</h2>



The researchers tagged the active neurons with fluorescent markers and saw a tight cluster in <a href="https://www.sciencedirect.com/topics/immunology-and-microbiology/hippocampal-ca1-region" target="_blank" rel="noreferrer noopener">hippocampal area CA1</a>. Destroying just that cluster erased the animals’ recollection of a prior feeding spot while leaving other spatial memories intact.



Calcium imaging showed the same cells projecting to the <a href="https://www.nature.com/articles/s12276-025-01451-y" target="_blank" rel="noreferrer noopener">lateral hypothalamus</a>, a region that governs hunger. Block that highway and the rats forgot where they last ate, then returned to the bowl sooner than usual.



The brain fails to properly catalog the meal experience when attention drifts, noted study lead author Lea Décarie‑Spain. This raises a practical concern for phone‑scrolling <a href="https://www.earth.com/news/earth-day-2025-what-were-really-fighting-for/" target="_blank" rel="noreferrer noopener">diners</a>.



<h2 class="wp-block-heading" id="h-how-memory-affects-meal-timing">How memory affects meal timing</h2>



Meal memories don’t just help us remember what we <a href="https://www.earth.com/news/how-our-brains-tell-us-when-we-need-to-eat-or-drink-neurons-hunger-thirst/" target="_blank" rel="noreferrer noopener">ate</a>, they also influence when we eat again. In rodent models, weakening this memory system led to shorter intervals between meals, while stronger engrams delayed the next eating session. 



The results suggest that our brains rely on memory to set an internal clock for hunger, not just fullness. In humans, this could explain why some people feel hungry soon after eating when their <a href="https://www.sciencedirect.com/science/article/pii/S0195666322002276" target="_blank" rel="noreferrer noopener">attention</a> was divided. 



If the brain fails to register that a meal happened, the hunger signal may reboot on a faster schedule, leading to more frequent snacking. This highlights how memory is just as important as metabolism when it comes to managing appetite.



<h2 class="wp-block-heading" id="h-when-meal-memory-fails">When meal memory fails</h2>



People with <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC10852764/" target="_blank" rel="noreferrer noopener">dementia</a> often eat back‑to‑back meals because the earlier one never registers. Clinical reports list overeating among the most common behavioral changes in late‑stage dementia.



Similar lapses can occur in healthy adults after a busy day. <a href="https://www.sciencedirect.com/science/article/pii/S0195666322005025" target="_blank" rel="noreferrer noopener">Imagining</a> a meal as larger or more satisfying cuts later cookie consumption, showing the brain’s bookkeeping matters.



<h2 class="wp-block-heading" id="h-the-distracted-eating-trap">The distracted eating trap</h2>



Modern life bombards us with screens that steal those pause‑and‑encode moments. Lab studies find that people who eat while multitasking consume more calories at the next opportunity.



Kanoski’s team argues that distraction weakens the hippocampal trace. Without a solid record, the hypothalamus treats the body as unfed and restarts the appetite drive.



This might help explain why eating at desks or in front of the TV is linked to unintentional weight gain. When the brain doesn’t register the meal, it leaves the hunger signal switched on.



<h2 class="wp-block-heading" id="h-meal-memory-and-hunger-control">Meal memory and hunger control</h2>



Neuroscientists have long known the hypothalamus pushes behavior like a gas pedal, yet what taps the pedal has been murkier. The current work shows that a direct line from the memory hub to the feeding hub times the signal.



The <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC4927193/" target="_blank" rel="noreferrer noopener">lateral hypothalamus</a> has a storied past in appetite research, housing neurons that boost seeking and reward. Earlier reviews mapped extensive circuits, but this hippocampal branch clarifies why timing matters.



<h2 class="wp-block-heading" id="h-implications-for-obesity-care">Implications for obesity care</h2>



Traditional weight‑loss plans emphasize willpower and portion control. The new data suggest that strengthening meal memory could be just as important.



Mindful eating programs already encourage slow, undistracted bites. By reinforcing the engram, such habits may reduce the urge for extra snacks later.



Pharmaceutical routes may follow. Kanoski’s group found that serotonin‑2A receptors on the same cells modulate the effect, suggesting a possible drug target.



<h2 class="wp-block-heading" id="h-tips-for-sharper-meal-memories">Tips for sharper meal memories</h2>



Sit at a table without your phone and notice the first and last bite. Tiny rituals like describing flavors out loud can anchor the episode in neural storage.



Pause for twenty seconds after swallowing, allowing the hippocampus its encoding window. Keep meals in consistent locations to help your brain form spatial associations.



Journaling meals shortly after eating may also help solidify the memory. Even a quick voice note could enhance recall and reinforce satiety.



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



The team plans to test whether similar neurons exist in humans using functional MRI. If so, brain‑stimulation trials might help people with overeating disorders rebuild the missing diary.



Nutrition scientists also want to see if high‑sugar or high‑fat foods blur the trace faster than protein‑rich meals. Such work could explain why some diets promote grazing behavior.



The research also holds implications for aging. If meal engrams degrade over decades, reinforcing them early might stave off later metabolic issues.



The study is published in the journal <a href="https://www.nature.com/articles/s41467-025-59687-1" target="_blank" rel="noreferrer noopener">Nature Communications</a>.



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Our brain has a 'meal memory' that controls hunger

Skipping a meal can feel like an open invitation to...

Roboticists have long dreamed of machines that can pick up an egg without cracking the shell and shake a hand without feeling wooden. Yet most robots still grasp the world through numbers, not nerves. 



That gap narrows today thanks to a stretchy gelatin “<a href="https://www.science.org/doi/10.1126/scirobotics.adq2303" target="_blank" rel="noreferrer noopener">skin</a>” that cloaks a <a href="https://www.earth.com/news/wildfusion-new-robots-can-use-multisensory-perception-to-map-rugged-terrain/" target="_blank" rel="noreferrer noopener">robotic</a> hand and turns the entire surface into a sensor.



<a href="https://www.eng.cam.ac.uk/profiles/dsh46" target="_blank" rel="noreferrer noopener">Dr. David Hardman</a> of the University of Cambridge and collaborators at <a href="https://www.ucl.ac.uk/about/" target="_blank" rel="noreferrer noopener">University College London</a> say the material collects touch data while costing only a few dollars to make.



<h2 class="wp-block-heading" id="h-why-robot-skin-must-feel-to-handle-objects-safely">Why robot skin must feel to handle objects safely</h2>



A hand without sensation is just a clamp. <a href="https://www.earth.com/news/robots-can-now-learn-from-humans-by-watching-how-to-videos/" target="_blank" rel="noreferrer noopener">Robots</a> used in warehouses or orchards often rely on cameras alone and can fumble soft or irregular objects, slowing adoption where safety and speed matter. 



Electronic skins that flex like human epidermis have been <a href="https://link.springer.com/article/10.1007/s40820-022-00911-8" target="_blank" rel="noreferrer noopener">investigated</a> for years, but many designs tear easily or rely on dozens of fragile sensor tiles.



Adding reliable touch also brings better prosthetics. Users of advanced bionic limbs report that even a coarse sense of pressure makes tying shoes easier because they no longer have to watch every movement. 



Engineers therefore hunt for materials that feel natural, conduct signals, and survive daily knocks.



<h2 class="wp-block-heading" id="h-cheap-skin-gives-robots-real-time-sensing">Cheap skin gives robots real-time sensing</h2>



The Cambridge UCL skin starts with a gelatin‑based <a href="https://www.sciencedirect.com/topics/chemistry/hydrogel" target="_blank" rel="noreferrer noopener">hydrogel</a> laced with conductive salt. The team melts the squishy mix, pours it into a glove‑shaped mold, and slips it onto an off‑the‑shelf robotic hand.



Signals are read using electrical impedance tomography (<a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC8667811/" target="_blank" rel="noreferrer noopener">EIT</a>), the same physics behind some medical imaging scanners. 



Thirty‑two copper electrodes at the wrist inject tiny currents and measure voltage patterns that ripple through more than 860 000 microscopic pathways in the gel.



“We’re able to squeeze a lot of information from these <a href="https://www.earth.com/news/autonomous-robots-are-revolutionizing-marine-operations/" target="_blank" rel="noreferrer noopener">materials</a> – they can take thousands of measurements very quickly,” said Hardman.



The hydrogel survives bending to 90 degrees and recovers after being cut and rejoined, a property shared with new <a href="https://www.nature.com/articles/s41467-024-53957-0" target="_blank" rel="noreferrer noopener">self‑healing electronic skins</a> reported this year.



<h2 class="wp-block-heading" id="h-what-millions-of-data-points-reveal">What millions of data points reveal</h2>



In lab tests the glove sensed a finger tap gentler than the weight of a penny and spotted a 248 °F hot spot in under one second. 



Those feats stem from the dense internal network: with a handful of electrodes the researchers harvested 1.7 million data points while the hand handled objects.



Extracting meaning from that torrent called for machine learning. The group trained an algorithm to focus on the pathways that change most under specific stimuli, letting the system tell slicing damage from a multipoint squeeze with 96 percent accuracy. 



Similar data‑driven pruning has boosted resolution in <a href="https://www.mdpi.com/1424-8220/24/18/5985" target="_blank" rel="noreferrer noopener">earlier</a> EIT skins made for soft robots. 



<h2 class="wp-block-heading" id="h-teaching-the-hand-to-interpret-touch">Teaching the hand to interpret touch</h2>



Raw impedance plots look like <a href="https://www.earth.com/news/robots-with-space-to-think-will-become-more-useful/" target="_blank" rel="noreferrer noopener">static</a> to the naked eye. After training, the glove could localize a light touch to within a quarter inch, estimate force to within 0.1 pound, and flag cuts long before they severed the gel.



“One type of sensor to detect multiple signals keeps manufacturing simple. We’re not quite at the level where the robotic skin is as good as human skin, but we think it’s better than anything else out there at the moment,” said <a href="https://tthuruthel.com/" target="_blank" rel="noreferrer noopener">Dr. Thomas George Thuruthel</a>.&nbsp;



Because the material is transparent to radio waves, the team foresees wireless versions that wrap soft drones or search‑and‑rescue grippers. 



A related <a href="https://www.nature.com/articles/s41467-024-50270-8" target="_blank" rel="noreferrer noopener">droplet‑tracking e‑skin</a> published last year shows how single‑layer designs can morph to meet niche tasks such as monitoring water quality. 



<h2 class="wp-block-heading" id="h-real-life-use-for-robotic-skin">Real-life use for robotic skin</h2>



Automakers already fill dashboards with capacitive touch film; an inexpensive layer that also senses heat and damage could warn drivers before components overheat. 



The skin might line collaborative‑robot grippers on factory floors, cutting downtime when humans walk by.



In prosthetics the gelatin makes a comfortable interface and could be infused with vitamins that keep residual limbs healthy. 



The material’s low cost (gelatin, salt, and a silicone jacket) also suits disposable medical tools such as soft retractors that alert surgeons if they press too hard.



<h2 class="wp-block-heading" id="h-how-it-compares-to-human-skin">How it compares to human skin</h2>



While the new material isn't as sensitive as human skin, it replicates some essential properties. It can register a range of stimuli, pressure, heat, sharp contact, from multiple points at once and across a continuous surface.



Human skin still outperforms it in fine resolution, regenerative ability, and biological integration. But the robotic version has an edge in durability, as it won’t scar or lose sensitivity over time.



<h2 class="wp-block-heading" id="h-what-s-next-for-robot-skin-research">What’s next for robot skin research</h2>



The group aims to toughen the hydrogel against ultraviolet light and dehydration, two weak spots shared by many water‑based gels. 



Coating the glove with a breathable elastomer similar to <a href="https://www.science.org/doi/10.1126/sciadv.ads1301" target="_blank" rel="noreferrer noopener">waterproof bandages</a> could triple shelf life without muffling signals. 



They also plan to shrink the electronics so a battery and radio fit in a fingertip. If that happens, the age‑old handshake between human and machine may finally feel familiar on both sides.



The study is published in <a href="https://www.science.org/doi/10.1126/scirobotics.adq2303" target="_blank" rel="noreferrer noopener">Science Robotics</a>.



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New 'electronic skin' gives robots the human touch

Roboticists have long dreamed of machines that can pick up...

Tiny mammals that weigh less than an ounce should not outlive German shepherds, yet many bats routinely do. Some even clock nearly thirty-five years in the wild, a lifespan that maps to about 180 human years and comes with an astonishing lack of tumors.



A <a href="https://www.rochester.edu/" target="_blank" rel="noreferrer noopener">University of Rochester</a> team set out to uncover why, zeroing in on four bat species spanning both major bat <a href="https://www.earth.com/news/bats-surf-the-winds-of-storms-during-migration/" target="_blank" rel="noreferrer noopener">lineages</a>. 



Their findings point to a finely tuned partnership between an overachieving tumor suppressor gene, self-renewing chromosomes, and an immune system that fights hard but rarely overreacts.



The work was led by Vera Gorbunova and Andrei Seluanov of the <a href="https://www.urmc.rochester.edu/cancer-institute">Wilmot Cancer Institute and Department of Biology</a>.



<h2 class="wp-block-heading" id="h-bats-defy-aging-and-cancer-patterns">Bats defy aging and cancer patterns</h2>



Cancer risk usually rises with age because every round of cell division adds another chance for DNA damage, a pattern known as <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC3060950/" target="_blank" rel="noreferrer noopener">Peto's paradox</a>. 



Across most <a href="https://www.earth.com/news/how-bats-navigate-noisy-world/" target="_blank" rel="noreferrer noopener">mammals</a> the equation holds, but bats are clear outliers, with at least four separate bat lineages independently evolving extreme <a href="https://pubmed.ncbi.nlm.nih.gov/30966896/" target="_blank" rel="noreferrer noopener">longevity</a>.



The new study shows that the “little brown” bat (<a href="https://www.fws.gov/species/little-brown-bat-myotis-lucifugus" target="_blank" rel="noreferrer noopener">Myotis lucifugus</a>) carries two working copies of the key tumor suppressor gene <a href="https://www.ncbi.nlm.nih.gov/books/NBK22268/" target="_blank" rel="noreferrer noopener">p53</a>, while humans carry only one. 



“High levels of p53 in the body can kill cancer cells before they become harmful in a process known as <a href="https://www.genome.gov/genetics-glossary/apoptosis" target="_blank" rel="noreferrer noopener">apoptosis</a>,” said Gorbunova.



<h2 class="wp-block-heading" id="h-understanding-myotis-lucifugus-the-basics">Understanding Myotis lucifugus - the basics</h2>



Better known as the little brown bat, Myotis lucifugus is one of the most widespread and familiar bat species in North America. You’ll often find them roosting in attics, barns, caves, and trees - basically anywhere cozy and dark. 



These bats are tiny, weighing less than half an ounce, but they pack a punch when it comes to eating insects. In a single night, one little brown bat can devour hundreds of mosquitoes and other bugs, making them natural pest controllers.



They usually hibernate during the winter, often gathering in large colonies where the temperature stays just right. Sadly, their populations have taken a major hit due to white-nose syndrome, a fungal disease that’s devastated colonies across the continent. 



Scientists and conservationists are working hard to figure out how to protect them, since losing these bats would ripple through entire ecosystems.



<h2 class="wp-block-heading" id="h-bats-use-extra-p53-to-stop-cancer">Bats use extra p53 to stop cancer</h2>



Duplicating p53 is not unique to bats; <a href="https://elifesciences.org/articles/11994" target="_blank" rel="noreferrer noopener">elephants</a> stockpile roughly twenty versions of the same gene and show remarkably low cancer rates. 



Bats, however, balance extra p53 with regulatory tweaks so it prunes precancerous cells without wiping out healthy ones.



“Our animals can tolerate faster cell growth because their p53 is ready to pull the plug when things look suspicious,” said Seluanov. 



The Rochester team found that <a href="https://www.earth.com/news/how-bats-navigate-rush-hour-without-crashing-into-each-other/" target="_blank" rel="noreferrer noopener">bat</a> cells need only two genetic “hits” to turn cancerous in a dish, far fewer than human cells, but the boosted p53 swiftly orders those rogue cells to self-destruct. 



<h2 class="wp-block-heading" id="h-endless-telomeres-controlled-chaos">Endless telomeres, controlled chaos</h2>



Bats also keep their chromosome tips long thanks to <a href="https://pubmed.ncbi.nlm.nih.gov/12034875/" target="_blank" rel="noreferrer noopener">constitutive telomerase</a>, an enzyme most adult human tissues silence. 



Earlier work in <a href="https://pubmed.ncbi.nlm.nih.gov/29441358/" target="_blank" rel="noreferrer noopener">Myotis</a> bats revealed that telomeres hardly shorten with age, helping tissues regenerate without sliding toward crisis.



Unfettered telomerase can fuel tumors in other species, yet bats avoid that pitfall. When telomere-powered cell divisions pick up speed, the same hyper-alert p53 system steps in, neutralizing any cell that crosses the line. 



“If cells divide uncontrollably, the higher p53 activity in bats compensates and can remove cancerous cells,” noted Seluanov.



<h2 class="wp-block-heading" id="h-how-bats-fight-disease">How bats fight disease</h2>



A third line of defense comes from a bat immune network that spots danger quickly but stays unusually calm. 



<a href="https://www.nature.com/articles/s41586-020-03128-0" target="_blank" rel="noreferrer noopener">Bats</a> mute the <a href="https://www.nature.com/articles/s41577-019-0165-0" target="_blank" rel="noreferrer noopener">NLRP3 inflammasome</a> and tone down <a href="https://www.nature.com/articles/nri3787" target="_blank" rel="noreferrer noopener">type I interferon</a> storms, preventing <a href="https://www.ncbi.nlm.nih.gov/books/NBK493173/" target="_blank" rel="noreferrer noopener">chronic inflammation</a> that often seeds cancer in aging tissues.



This balanced <a href="https://www.sciencedirect.com/topics/medicine-and-dentistry/immunosurveillance" target="_blank" rel="noreferrer noopener">immune surveillance</a> means viruses are cleared efficiently and damaged cells are flagged for destruction, yet surrounding tissue is spared collateral damage. 



Researchers also report expanded natural killer cell receptor families in several bat genomes, hinting at a surveillance squad that never sleeps.



<h2 class="wp-block-heading" id="h-what-bats-can-teach-us-about-treating-cancer">What bats can teach us about treating cancer</h2>



Several experimental drugs already seek to boost human p53 activity in stubborn tumors, and the bat data give that strategy an evolutionary vote of confidence. 



Others aim to reactivate telomerase in aged tissues; the <a href="https://www.earth.com/news/bats-have-acoustic-mental-maps-to-navigate-total-darkness/" target="_blank" rel="noreferrer noopener">bat</a> blueprint suggests that pairing such therapies with stronger p53 safeguards could keep runaway cell growth in check.



<a href="https://www.nia.nih.gov/" target="_blank" rel="noreferrer noopener">The National Institute on Aging</a> funded the study because it touches on two grand challenges: healthy longevity and cancer prevention. 



If scientists can replicate the bat trio of robust p53, restrained inflammation, and prudent telomerase, future therapies might tackle both aging and malignancy in one stroke.



<h2 class="wp-block-heading" id="h-what-other-animals-can-teach-us">What other animals can teach us</h2>



Scientists have long looked to other long-lived animals for answers. 



<a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC10492090/" target="_blank" rel="noreferrer noopener">Naked mole rats</a>, <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC11580846/" target="_blank" rel="noreferrer noopener">bowhead whales</a>, and elephants each have their own anti-cancer tricks, ranging from extra copies of tumor suppressor genes to unique cell death responses. 



Bats now join this elite group, and their diverse adaptations offer a different evolutionary path toward disease resistance.



These findings also support the case for cross-species genetic studies in humans. 



If p53 enhancements or telomerase tuning can be translated safely, it could lead to preventive therapies for high-risk populations or those with inherited cancer mutations. 



What bats seem to offer is not a miracle gene, but a blueprint for managing cellular risk while still allowing the body to repair, grow, and age slowly.



The study is published in <a href="https://www.nature.com/articles/s41467-025-59403-z" target="_blank" rel="noreferrer noopener">Nature Communications</a>.



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Bats don't get cancer, now scientists think they know the reason

Tiny mammals that weigh less than an ounce should not...

Timekeepers once trusted wobbling pendulums and vibrating quartz. Now, the world’s best quantum clocks probe energy gaps inside single atoms, counting oscillations with parts‑per‑quintillion precision.



Professor Marcus Huber of the Atomic Institute at <a href="https://www.tuwien.at/" target="_blank" rel="noreferrer noopener">TU Wien</a> and his collaborators have upended a rule that many physicists treated as gospel: double the accuracy, double the energy bill.



<h2 class="wp-block-heading" id="h-old-clocks-needed-more-energy">Old clocks needed more energy </h2>



Every clock marries a periodic event to a counter. The event must reset, but the counter must not, so each tick irreversibly shuffles some <a href="https://www.earth.com/news/new-form-of-quantum-entanglement-discovered-will-transform-next-gen-technology/" target="_blank" rel="noreferrer noopener">entropy</a> into the surroundings, whether as heat, light, or molecular jostling.



For classical devices the link looks linear. Push a pendulum harder or fire a brighter laser, and you do suppress statistical noise, but only in lockstep with the fuel burned. 



This intuition was formalized in the <a href="https://www.nature.com/articles/s41567-019-0702-6" target="_blank" rel="noreferrer noopener">thermodynamic uncertainty relation</a>, a bound <a href="https://link.aps.org/doi/10.1103/PhysRevLett.128.130606" target="_blank" rel="noreferrer noopener">suggesting</a> that precision cannot outpace dissipation.



<h2 class="wp-block-heading" id="h-tracking-time-with-two-motions">Tracking time with two motions</h2>



Huber’s team realized the bound is not a wall but a loophole waiting for the right architecture. They built a virtual ring of quantum sites, let one excitation circulate freely, and added a single lossy <a href="https://www.earth.com/news/new-form-of-quantum-entanglement-discovered-will-transform-next-gen-technology/" target="_blank" rel="noreferrer noopener">junction</a> that “clicks” whenever the particle completes a lap.



One motion is fast and coherent, spreading like a wave and costing no entropy. The other motion (crossing the junction) happens rarely and irreversibly, acting like the minute hand.



“Combining a swift, entropy‑free shuttle with a slow, entropy‑producing register gives an exponential gain in accuracy per unit cost,” explained Florian Meier, a PhD student at the Atominstitut at TU Wien.



<h2 class="wp-block-heading" id="h-achieving-precision-with-less-energy">Achieving precision with less energy</h2>



Simulations show the clock’s precision scales roughly as the chain length to the 4⁄3 power while the needed entropy grows only <a href="https://www.oed.com/dictionary/logarithmically_adv?tl=true" target="_blank" rel="noreferrer noopener">logarithmically</a>. In other words, each extra bit of dissipation can buy orders of magnitude better timing.



“Superconducting circuits already give us all the ingredients to test this idea in hardware,” noted study co‑author Simone Gasparinetti. 



Earlier <a href="https://www.nist.gov/programs-projects/yb-optical-lattice-clock" target="_blank" rel="noreferrer noopener">optical lattice clocks</a> achieve parts‑in‑10¹⁸ stability yet still waste far more energy than Huber’s design would need at the same precision.



<h2 class="wp-block-heading" id="h-quantum-clock-and-future-tech">Quantum clock and future tech</h2>



Low‑dissipation timing matters once devices shrink to the nanoscale or fly deep in space, where <a href="https://www.earth.com/news/quantum-gates-teleported-a-leap-toward-scalable-computing/" target="_blank" rel="noreferrer noopener">power</a> budgets are tight. 



Quantum networks, for example, must distribute photons on picosecond schedules; swapping today’s power‑hungry drivers for a passive ring clock could simplify that task.



Precision gravimetry and navigation also benefit, since every tick saved from thermal noise translates to clearer signals. If validated in the lab, the method might trim the roadmap for redefining the second, now slated for <a href="https://www.ft.com/content/625d2043-a5a4-4d6d-bbe9-42e524a211dd" target="_blank" rel="noreferrer noopener">2030</a>.



<h2 class="wp-block-heading" id="h-quantum-clock-design-reduces-waste">Quantum clock design reduces waste</h2>



The researchers engineered their ring clock using <a href="https://www.nature.com/articles/srep25157" target="_blank" rel="noreferrer noopener">coherent transport</a>, a process where quantum particles glide across the chain without loss. Only when the particle completes a full cycle does it interact with the environment, generating entropy.



This design sharply contrasts with fully dissipative clocks that register every tick by interrupting the system. Because only one segment of the ring needs to be thermodynamically active, most of the clock runs “clean,” saving energy.



“We’re not claiming magic. It’s still irreversible when a tick occurs. But quantum effects let us delay and localize that cost,” said Huber. 



<h2 class="wp-block-heading" id="h-stability-of-the-quantum-clock">Stability of the quantum clock</h2>



To ensure real‑world feasibility, the team simulated noise, disorder in coupling strengths, and unwanted dissipation. 



The experts found that the clock still holds up well: the performance drop is gradual, and the accuracy gain remains impressive if imperfections are kept modest.



The needed physical platform already exists. Superconducting <a href="https://journals.aps.org/pra/abstract/10.1103/PhysRevA.86.023837" target="_blank" rel="noreferrer noopener">coupled cavity arrays</a> can host hundreds of sites with tunable couplings and minimal loss.



Tick events could be detected via microwave photon counters or continuous readout of artificial atoms, techniques already tested in <a href="https://journals.aps.org/rmp/abstract/10.1103/RevModPhys.93.025005" target="_blank" rel="noreferrer noopener">circuit quantum electrodynamics</a>.



<h2 class="wp-block-heading" id="h-implications-for-quantum-tech">Implications for quantum tech</h2>



Quantum clocks like the ring model don’t just sharpen timekeeping, they push the boundaries of what self-contained quantum devices can do. 



As researchers strive for scalable quantum networks and portable quantum sensors, designs that minimize external control and internal dissipation become increasingly important.



The principle behind this clock could influence fields beyond metrology. Engineers designing quantum repeaters, synchronizers, or energy-efficient processors might borrow the same structure: localized thermodynamic cost, distributed coherent transport.



<h2 class="wp-block-heading" id="h-rethinking-thermodynamic-limits">Rethinking thermodynamic limits</h2>



Does the result violate thermodynamics? No, the second law still demands that entropy increase somewhere; Huber’s trick merely spends it sparingly by letting quantum coherence shoulder most of the workload.



The work also hints that the familiar arrow of time, stitched from countless microscopic irreversibilities, is compatible with islands of near‑reversible quantum motion. That insight could ripple beyond metrology into quantum control and information theory.



The study is published in the journal <a href="https://www.nature.com/articles/s41567-025-02929-2" target="_blank" rel="noreferrer noopener">Nature Physics</a>.



Image Credit: Alexander Rommel



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Quantum clock revolution could change how we measure time

Timekeepers once trusted wobbling pendulums and vibrating quartz. Now, the...

Should humans ever pull the plug on a living species? Advances in genome editing make that possibility concrete, and a recent study asks when, if ever, such power is justified.



The researchers weighed the suffering caused by pests against the intrinsic worth of <a href="https://www.worldwildlife.org/pages/what-is-biodiversity" target="_blank" rel="noreferrer noopener">biodiversity</a>, setting a high bar for intentional wipeouts. Their conclusion is that genetically erasing a species might be acceptable, but only under exceptional, tightly bounded circumstances.



<h2 class="wp-block-heading" id="h-when-erasing-a-species-feels-necessary">When erasing a species feels necessary</h2>



“This question keeps conservationists up at night,” said Dr. Clare Palmer of <a href="https://www.tamu.edu/" target="_blank" rel="noreferrer noopener">Texas A&amp;M University</a> after helping draft the report. She and colleagues argue that an animal’s capacity to cause widespread agony can, in rare cases, outweigh its right to persist.



Ethicists usually treat biodiversity as a moral good, yet real-world conflicts force tough trade-offs. When an insect’s life hinges on a calf’s ability to survive, abstract principles meet muddy pens and medical bills.



Most philosophies rank individual suffering above abstract species value once pain passes a certain threshold. Even ecologists concede that leaving sentient creatures to suffer avoidable harm strains any theory of non-intervention.



<h2 class="wp-block-heading" id="h-three-cases-in-focus">Three cases in focus</h2>



The parasitic screwworm (<a href="https://www.aphis.usda.gov/livestock-poultry-disease/cattle/ticks/screwworm" target="_blank" rel="noreferrer noopener">Cochliomyia hominivorax</a>) burrows into the flesh of livestock and wildlife, killing thousands of animals every year before treatment can begin. The United States eliminated native populations in 1966 using the Sterile Insect Technique (<a href="https://www.iaea.org/topics/sterile-insect-technique" target="_blank" rel="noreferrer noopener">SIT</a>).



Mosquitoes of the species <a href="https://www.sciencedirect.com/topics/neuroscience/anopheles-gambiae" target="_blank" rel="noreferrer noopener">Anopheles gambiae</a> spread <a href="https://www.who.int/news-room/fact-sheets/detail/malaria" target="_blank" rel="noreferrer noopener">malaria</a>, a disease that took an estimated 597,000 lives in 2023 alone - most of them children under five.



Those numbers eclipse fatalities from many better-publicized illnesses and keep public-health agencies searching for stronger tools.



On South Africa’s Marion Island, the humble house mouse (<a href="https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=info&amp;id=10090" target="_blank" rel="noreferrer noopener">Mus musculus</a>) has started gnawing seabird chicks alive, pushing several albatross species toward local collapse. Conventional traps fail on rugged slopes, and poison risks collateral damage to native invertebrates.



<h2 class="wp-block-heading" id="h-how-scientists-can-erase-species">How scientists can erase species</h2>



The Sterile Insect Technique remains the standard for humane pest control. Irradiated males mate but produce no viable young, gradually crashing the target population without pesticides.



A newer option, the <a href="https://royalsocietypublishing.org/doi/10.1098/rspb.2019.1606" target="_blank" rel="noreferrer noopener">gene drive</a>, moves lethal or sex-skewing genes through wild populations so quickly that normal inheritance rules break down. 



Researchers working with rodents have already demonstrated systems that turn almost every embryo male, guaranteeing eventual collapse.



For mosquitoes, scientists can now couple a drive to a gene that blocks parasite replication, reducing disease transmission rather than eliminating the insect outright. Palmer’s team notes that such restraint might satisfy the same moral aims with less ecological upheaval.



<h2 class="wp-block-heading" id="h-killing-pests-sometimes-gains-approval">Killing pests sometimes gains approval</h2>



“Together, we argue, these cases suggest that deliberate full extinction might occasionally be acceptable, but only extremely rarely,” the authors wrote. Where pests impose unrelenting misery on humans or endangered wildlife, even cautious ethicists lean toward eradication.&nbsp;



In farm economies, screwworm outbreaks once cost ranchers hundreds of millions of dollars each year. 



The <a href="https://www.ncba.org/news-media/news/details/43094/ncba-pushes-for-domestic-sterile-fly-facility-to-eradicate-new-world-screwworm" target="_blank" rel="noreferrer noopener">sterile-fly program</a> reduced those losses while sparing cattle surgeries and antibiotic use, making SIT a textbook case of net welfare gain.



<h2 class="wp-block-heading" id="h-risks-and-safeguards">Risks and safeguards</h2>



No <a href="https://bmcmedethics.biomedcentral.com/articles/10.1186/s12910-021-00588-5" target="_blank" rel="noreferrer noopener">drive</a> can be recalled once released. If a sex-skewing construct escaped from an island to a mainland, the entire species could vanish before regulators reacted. That possibility drives calls for redundant containment layers and staged testing.



Wild genomes hold surprises such as mating behavior, migration corridors, or hidden ecological roles. 



Removing a dominant mosquito might allow a harder-to-control sibling species to fill the gap, canceling health gains while shackling communities to continuous editing cycles.



Governance frameworks must also weigh cultural values. Some communities view rats as food, while others see them as vermin. A one-size rule will not work in global treaties.



<h2 class="wp-block-heading" id="h-who-should-decide-to-erase-a-species">Who should decide to erase a species?</h2>



Palmer and colleagues insist that village councils, livestock owners, conservation NGOs, and public health officials should share equal seats at the table. Only broad consent can legitimize an action that removes a lineage that is millions of years old.



The study suggests that formal benefit-harm ledgers need to be updated as new data emerge. There is also a need for sunset clauses that halt projects if early milestones falter. Robust monitoring budgets must be in place before the first transgenic egg hatches.



Funding streams pose another dilemma. Genome projects often depend on philanthropic donors from far away. Affected regions need guaranteed control over long-term stewardship, including the power to veto deployment.



<h2 class="wp-block-heading" id="h-the-fast-pace-of-technology">The fast pace of technology </h2>



Current international regulations lag behind the pace of synthetic biology. While conventions like the <a href="https://bch.cbd.int/protocol" target="_blank" rel="noreferrer noopener">Cartagena Protocol</a> aim to manage genetically modified organisms, they do not directly address deliberate extinction by gene drive.



This leaves a grey area where cross-border impacts, like species drifting across national boundaries, may not fall under clear legal control. Coordinated policy development is needed to prevent gaps that bad actors or accidents could exploit.



The World Health Organization and United Nations Environment Programme have both called for more robust oversight. However, the tools available for enforcement are often limited to guidance rather than mandates, leaving implementation up to individual nations.



The researchers say it’s critical to close these gaps before large-scale extinction drives become common, especially given how rapidly the technology is evolving.



<h2 class="wp-block-heading" id="h-the-future-of-gene-drives">The future of gene drives</h2>



<a href="https://www.genome.gov/genetics-glossary/CRISPR" target="_blank" rel="noreferrer noopener">CRISPR</a> keeps shrinking the cost and time required to build custom drives, so ethical debates must stay a step ahead of lab capacity. 



Palmer hopes that clear rules will prevent both reckless releases and sweeping bans that deny relief to suffering animals. She sees the conversation itself as a sign of progress. 



Past generations used lead arsenate or DDT with little scrutiny. Today, genetic strategies face hard questions before a single insect leaves quarantine.



The study is published in the journal <a href="https://www.science.org/doi/10.1126/science.adv4045" target="_blank" rel="noreferrer noopener">Science</a>.



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Extinction by design: Should we genetically erase harmful species?

Should humans ever pull the plug on a living species?...

Biodiversity is declining across Japan’s countryside, even as villages empty and young people move to the cities. Many would expect birds, insects, and native plants to return when humans leave. A new study shows that’s not happening.



The research team examined land-use change, temperature records, and nearly two decades of citizen-science observations.



<h2 class="wp-block-heading" id="h-population-loss-doesn-t-equal-biodiversity-gain">Population loss doesn’t equal biodiversity gain</h2>



The researchers mapped population change across rural Japan and overlaid 1.5 million sightings of 464 animal species and 2,922 plant species collected between 2004 and 2021. 



Shrinking towns did not rebound ecologically. Instead, abandoned rice fields turned into either housing estates or weed-choked lots. Both outcomes hurt wildlife.



Study co-author Dr Peter Matanle is a senior lecturer in Japanese Ssudies at the <a href="https://www.sheffield.ac.uk/" target="_blank" rel="noreferrer noopener">University of Sheffield</a>.



“Japan is one of many countries whose demographic trends point to long-term population loss. We call it a 'Depopulation Vanguard Country' because it presages losses in similar neighboring countries such as South Korea and China," said Dr. Matanle.



“We find that expected biodiversity gains from fewer people may not be occurring, and that losses are continuing. This indicates possible similar effects in other world regions such as Southern Europe, with Italy as its DVC, and Eastern Europe, with Bulgaria and Latvia as its DVCs. 



Dr. Matanle noted that his team would like to study other regions in the future such as Europe and Latin America to find out if similar effects are being felt there.



<h2 class="wp-block-heading" id="h-citizen-scientists-fill-the-data-gap">Citizen scientists fill the data gap</h2>



Volunteers across Japan recorded birds, butterflies, fireflies, frog spawn, and local flora. Their notebooks and apps supplied one of the richest ecological datasets on Earth. 



The study shows how community monitoring can spot silent declines that official surveys might miss.



The study suggests that modest, steady farming often supports more life than sudden abandonment. When fields are left untended, invasive weeds can outcompete native plants. Without people to manage canals and paddies, wetlands dry out and the species they harbor disappear.



<h2 class="wp-block-heading" id="h-traditional-practices-support-biodiversity">Traditional practices support biodiversity </h2>



“Japan’s biodiversity has long been sustained by traditional rural livelihood practices such as wet rice agriculture, forest and soil management, and the maintenance of rural landscapes. These human activities have shaped and supported ecological richness for centuries," said Kei Uchida, an associate professor at Tokyo City University.



“Even as populations decline, human interventions continue in some areas, while others are left to ecological succession. This uneven pattern of change produces a mosaic landscape which is accelerating the degradation of rural environments and undermining the biodiversity they support."



According to Professor Uchida, the research has implications for maintaining biodiversity in other depopulating countries in East Asia, and contributes to knowledge about the outcomes of human depopulation worldwide.



<h2 class="wp-block-heading" id="h-population-loss-is-a-global-issue">Population loss is a global issue</h2>



The United Nations expects 85 countries to decline in population by 2050, including much of Eastern and Southern Europe. The researchers urge governments to blend rewilding with rural job programs so that landscapes do not slide into neglect.



Shorter workweeks for farmers, subsidies for low-impact cultivation, and support for local wildlife groups are among the proposed ideas.



The lesson is clear: people leaving an area can harm nature as easily as they can help it. Careful planning is needed to tip the balance toward recovery.



<h2 class="wp-block-heading" id="h-population-and-biodiversity-loss">Population and biodiversity loss</h2>



Biodiversity loss is not just a local issue - it’s a global concern that affects ecosystems, economies, and everyday life. The decline of species, whether plants, insects, or animals, disrupts food chains, weakens soil health, and reduces the resilience of natural systems. 



When biodiversity shrinks, the services ecosystems provide - like pollination, water purification, and climate regulation - begin to break down.



In Japan, the study highlights how biodiversity continues to decline even as people leave rural areas. But similar trends are being seen worldwide, in both developed and developing regions. 



Land-use change, habitat fragmentation, invasive species, pollution, and climate change all contribute to the problem. Even regions experiencing depopulation are not immune - sometimes, they’re more vulnerable if the land is mismanaged or neglected.



<h2 class="wp-block-heading" id="h-new-strategies-to-protect-wildlife">New strategies to protect wildlife</h2>



This research adds to the growing body of evidence that simply removing human pressure isn’t always enough. 



Without intentional support, many landscapes fail to recover. Rewilding, conservation, and traditional ecological practices all have a role to play in reversing the loss. 



As countries face changing demographics and population loss, preserving biodiversity will require new strategies that account for both ecological and social realities.



The full study was published in the journal <a href="https://www.nature.com/articles/s41893-025-01578-w" target="_blank" rel="noreferrer noopener">Nature Sustainability</a>.



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Population loss in Japan's countryside linked to declining biodiversity

Biodiversity is declining across Japan’s countryside, even as villages empty...

Dogs aren’t just companions who brighten our daily routines. They may also be key players in monitoring how Valley fever moves through certain regions in the United States.



This disease, also called coccidioidomycosis, involves inhaling fungal spores found in dry soil conditions. 



<a href="http://vetmed.ucdavis.edu/faculty/jane-sykes" target="_blank" rel="noreferrer noopener">Jane Sykes</a>, lead author of a recent <a href="https://www.vetmed.ucdavis.edu/" target="_blank" rel="noreferrer noopener">UC Davis</a> study, worked with her team to see how information from dog infections could apply to humans.



<h2 class="wp-block-heading" id="h-understanding-valley-fever">Understanding Valley fever</h2>



When disturbed by wind, construction, or agricultural activity, the spores of <a href="https://www.sciencedirect.com/topics/immunology-and-microbiology/coccidioides-immitis" target="_blank" rel="noreferrer noopener">Coccidioides immitis</a> and <a href="https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/coccidioides-posadasii" target="_blank" rel="noreferrer noopener">Coccidioides posadasii</a> can ride on dust particles and travel into the lungs.



Some pets like to dig into dirt, creating an ideal chance to breathe in fungal particles. These Valley fever spores thrive in the Western parts of the country, often in places with specific soil moisture levels.



Though many people who are exposed may not experience symptoms, those who do often report flu-like illness, including fatigue, cough, fever, chest pain, and muscle aches.



In some cases, especially in individuals with weakened immune systems, Valley fever can become severe, spreading from the lungs to other parts of the body such as the skin, bones, joints, or even the brain, where it may cause <a href="https://www.earth.com/news/harmful-microbes-persist-on-hospital-surfaces-after-disinfection/" target="_blank" rel="noreferrer noopener">meningitis</a>. 



Diagnosis is typically confirmed through blood tests or imaging, and while mild cases often resolve without treatment, antifungal medications like fluconazole are prescribed for moderate to severe infections.



<h2 class="wp-block-heading" id="h-unusual-canine-clues">Unusual canine clues</h2>



The researchers discovered patterns by checking large collections of <a href="https://www.earth.com/news/lost-in-translation-how-we-misread-our-dogs-emotions/">dog</a> blood tests. 



They found that most positive results are linked to certain states with known contamination zones, but they also noticed smaller clusters appearing in locations not typically flagged for this infection.



“Dogs are sentinels for human infections,” said Jane Sykes. 



Her team collected blood test data in different areas to <a href="https://www.cdc.gov/valley-fever/about/index.html" target="_blank" rel="noreferrer noopener">identify rising trends</a> and potential health concerns for people.



<h2 class="wp-block-heading" id="h-what-puts-dogs-at-risk">What puts dogs at risk</h2>



Some vets <a href="https://vfce.arizona.edu" target="_blank" rel="noreferrer noopener">note</a> that certain breeds may be more prone to lung ailments, but any fungus exposure can be an issue. 



This might involve dusty backyards, fields, or construction sites, where spores in the soil can become airborne.



In regions with droughts or strong winds, soil dryness allows fungal particles to swirl into the air. Intense rainfall can also boost <a href="https://today.ucsd.edu/story/dangerous-airborne-fungus-boosted-by-california-droughts" target="_blank" rel="noreferrer noopener">fungal growth</a>, which further contributes to sporadic spikes in infection.



Researchers see these canine cases as indicators for possible spread in the broader population. Common symptoms in people include fatigue, cough, and sometimes sore joints.



Health agencies note that valley fever can become serious for those with weakened immune systems. Because dogs are tested more readily in certain regions, their results may warn us before human cases spike.



<h2 class="wp-block-heading" id="h-mapping-valley-fever-in-new-zones">Mapping valley fever in new zones</h2>



Scientists have spotted positive <a href="https://www.earth.com/news/uncovering-the-truth-the-reality-behind-canine-dna-testing/">canine</a> cases outside historically recognized areas. Jane Sykes explained that pockets of infection can appear in nearby states that might be overlooked.



“We should be closely watching those states because there could be under-recognition,” she said. This under-recognition means some doctors in these regions may not be aware of the disease and could miss early signs in humans.



Decades of shifting <a href="https://www.noaa.gov/education/resource-collections/climate/climate-change-impacts" target="_blank" rel="noreferrer noopener">climate patterns</a> have altered soil conditions. Over 130 places in the United States have recorded heavier bursts of rain in recent years, raising concerns about potential fungal growth when storms finally soak the land.



As new weather extremes develop, the fungus might have more opportunities to spread. Researchers keep emphasizing how environmental changes can shift the boundaries of diseases, leading to surprises in <a href="https://www.earth.com/news/covid-virus-can-remain-in-sperm-months-after-infection/">infection</a> data.



<h2 class="wp-block-heading" id="h-protecting-yourself-and-your-pet">Protecting yourself and your pet</h2>



Many dog owners wonder if this infection is preventable. Avoiding areas with visible dust clouds is one measure, though it can be tough when your pet loves running outdoors.



Some <a href="https://pubmed.ncbi.nlm.nih.gov/30690600/" target="_blank" rel="noreferrer noopener">vets</a> provide guidance on ways to limit exposure if your area is known for this fungus. 



Though these spores are hard to avoid entirely, regular checkups and early tests may help pets and owners stay aware of new health risks.



Veterinarians who live in spots with many valley fever cases watch for respiratory problems in dogs. A sudden cough or limp can signal hidden issues, prompting tests that reveal infection.



If caught early, there are antifungal treatments that can relieve symptoms. The goal is to manage lung damage and reduce further spread.



<h2 class="wp-block-heading" id="h-dogs-valley-fever-and-the-future">Dogs, valley fever, and the future</h2>



Researchers who track these <a href="https://www.earth.com/news/covid-infection-equips-the-body-to-fight-off-the-flu/">infections</a> see a bigger picture beyond local hotspots. They hope more states will gather accurate data so public health teams can warn residents who may be at risk.



Better knowledge about where the spores hide allows for timely alerts. Clear communication between veterinarians and medical professionals could help limit the toll on both animals and people.



Trends linked to heavy rain, population growth, and soil changes highlight the complexity of valley fever. Officials suggest that improved teaching for doctors could keep illness from going unnoticed.



Dogs may help identify emerging dangers because their health data can fill the gaps where human data are patchy. Scientists remain hopeful that continued studies will keep the public informed about this evolving fungal risk.



The study is published in the <a href="https://academic.oup.com/jid/article/231/5/e986/8108831?login=false" target="_blank" rel="noreferrer noopener">Journal of Infectious Diseases</a>.



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Scientists discover that dogs can alert humans to this quickly-spreading disease

Dogs aren’t just companions who brighten our daily routines. They...

Among tens of thousands of ant species, many show complex behaviors like agriculture and tool use. Longhorn crazy ants add a new twist to that story. Their brains are minuscule, but they manage coordinated, goal-oriented actions. 



A recent study shows that these ants can clear obstacles from a path before a food load even arrives. This action seems to require planning, yet it emerges without any <a href="https://www.earth.com/news/when-you-give-caffeine-to-ants-many-interesting-things-happen/" target="_blank" rel="noreferrer noopener">ant</a> holding a clear mental map.



Dr. Ehud Fonio, a scientist at the <a href="https://www.weizmann.ac.il/pages/" target="_blank" rel="noreferrer noopener">Weizmann Institute of Science</a>, is the lead author of the study.



“Here we show for the first time that workers of the longhorn crazy ant can clear obstacles from a path before they become a problem - anticipating where a large food item will need to go and preparing the way in advance," said Dr. Fonio.



"This is the first documented case of ants showing such forward-looking behavior during cooperative transport."



<h2 class="wp-block-heading" id="h-ants-plan-ahead-for-obstacles">Ants plan ahead for obstacles </h2>



The team made their discovery during fieldwork at the Weizmann Institute. Ants were seen removing pebbles before a food-carrying group arrived. This suggested some form of anticipation.



“When we first saw <a href="https://www.earth.com/news/how-many-ants-live-on-earth-at-any-point-in-time-total-number-is-astounding/" target="_blank" rel="noreferrer noopener">ants</a> clearing small obstacles ahead of the moving load we were in awe. It appeared as if these tiny creatures understand the difficulties that lie ahead and try to help their friends in advance,” said Dr. Ofer Feinerman, co-author of the study.



This chance observation led to a large-scale experiment involving 83 trials. The team replaced pebbles with plastic beads and placed cat food as bait. 



Ants cleared beads that blocked the path between food and nest, but only when the food was intact.



<h2 class="wp-block-heading" id="h-crazy-ants-clear-the-way-for-big-food">Crazy ants clear the way for big food</h2>



The ants cleared beads mainly when a single large pellet was present. With crumbs, they rarely cleared anything. This shows context sensitivity. Bead clearing happened only when it helped the group.



Ants transported the beads short distances, around 50 millimeters. They placed them away from the nest-food corridor. This effort reduced the food transport time by up to 15 times.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/06/longhorn-crazy-ants_carrying-bead_credit-Alessandro-Crespi_1big.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/06/longhorn-crazy-ants_carrying-bead_credit-Alessandro-Crespi_1s.webp" alt="Worker of longhorn crazy ant clearing a bead. Credit: Alessandro Crespi" class="wp-image-1973861"/></a><figcaption class="wp-element-caption">Worker of longhorn crazy ant clearing a bead. Click image to enlarge. Credit: Alessandro Crespi</figcaption></figure>



When large pellets were pinned down and could not be moved, <a href="https://www.earth.com/news/invasive-ants-have-found-a-new-way-to-spread-across-the-globe-on-cars/" target="_blank" rel="noreferrer noopener">ants</a> still cleared obstacles. But they ignored beads completely when no food or only crumbs were present.



<h2 class="wp-block-heading" id="h-ants-respond-to-scent-not-sight">Ants respond to scent, not sight</h2>



The study’s most surprising finding was that ants began clearing without even seeing or touching the food. The trigger? Fresh pheromone markings left by recruiters.



Even without food, these chemical signals caused some ants to start clearing beads. Of 155 observed ant-bead interactions, 97.2 percent were preceded by a nearby scent mark.



Direct contact with food was not necessary. Just encountering a pheromone trail within a 20 mm radius of a bead triggered clearing. This suggests that the behavior is socially driven, not based on internal plans.



<h2 class="wp-block-heading" id="h-collective-intelligence-of-ant-colonies">Collective intelligence of ant colonies</h2>



The experts discovered that crazy ants use a decentralized form of cognition. Instead of individual planning, their colony acts like a brain. 



Each ant is a unit responding to chemical cues. Together, they clear obstacles as if they understand the goal.



“Taken together, these results imply that our initial impression was wrong: in reality, individual workers don’t understand the situation at all. This intelligent behavior happens at the level of the <a href="https://www.earth.com/news/paleontologists-found-the-oldest-ant-species-on-earth-113-million-years-old-with-scythe-like-jaws/" target="_blank" rel="noreferrer noopener">colony</a>, not the individual," explained study co-author Dr. Danielle Mersch.



"Each ant follows simple cues - like fresh scent marks left by others - without needing to understand the bigger picture, yet together they create a smart, goal-directed outcome."



“We find this to be even more awe-inspiring than our initial guess,” said Feinerman.



<h2 class="wp-block-heading" id="h-simple-rules-for-complex-behavior">Simple rules for complex behavior </h2>



Interestingly, some ants cleared multiple beads in sequence. One ant removed 64 beads. These "serial clearers" often focused on the same sector around the food, repeatedly working in the same direction.



Some switched sectors but returned to old ones. This pattern hints at possible short-term memory or chemical trail-following. Researchers suggest these ants could be following pheromone gradients repeatedly.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/06/longhorn-crazy-ants_intelligence_swarm_credit-E-Fonio_1m.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/06/longhorn-crazy-ants_intelligence_swarm_credit-E-Fonio_1s.webp" alt="Examples of experimental set-up and close-up of collective transport of prey and of obstacle-clearing behavior. Credit: E Fonio, D Mersch, O Feinerman" class="wp-image-1973864"/></a><figcaption class="wp-element-caption">Examples of experimental set-up and close-up of collective transport of prey and of obstacle-clearing behavior. Click image to enlarge. Credit: E Fonio, D Mersch, O Feinerman</figcaption></figure>



The research shows how complex behavior emerges from simple rules. It also highlights the power of external memory. Pheromone trails serve as shared information banks etched into the environment.



In this system, memory and action are collective. No single ant plans ahead. Yet their joint behavior gives the illusion of foresight. This mirrors how neurons form intelligent thought in the human brain.



<h2 class="wp-block-heading" id="h-significance-of-ant-intelligence">Significance of ant intelligence </h2>



This work changes how we think about planning in nature. It shows that meaningful coordination does not require conscious intent. 



In ants, intelligent-seeming food-related outcomes arise from distributed actions and shared cues. These findings deepen our understanding of swarm behavior. 



The study also suggests new directions for robotics, where machines could collaborate without central control by using simple signals.



The study is published in the journal <a href="https://www.frontiersin.org/journals/behavioral-neuroscience/articles/10.3389/fnbeh.2025.1533372/full" target="_blank" rel="noreferrer noopener">Frontiers in Behavioral Neuroscience</a>.



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Swarm intelligence: Ants can anticipate obstacles and plan ahead

Among tens of thousands of ant species, many show complex...

When scientists on a <a href="https://www.hi.no/en/hi/news/2021/october/after-being-trapped-in-norway-by-the-pandemic,-dr.-fridtjof-nansen-is-once-again-heading-out-into-the-world">research vessel</a> off the northwestern coast of Africa hauled in their catch, they were surprised to find an unusual eel that did not match any known species. The 2-foot (0.6 meter) curiosity had fang-like teeth and a pointed head that set it apart.



It has now been identified it as a spoon-nose eel from the genus Mystriophis, and it has been named Mystriophis caboverdensis. It remains the only documented example of its kind.



According to <a href="https://www-iuem.univ-brest.fr/paddle/project/team/da-luz-alciany" target="_blank" rel="noreferrer noopener">Dr. Alciany Nascimento da Luz</a>, who was part of an international team collaborating with marine research institutes in Cabo Verde, this eel marks a special moment for local biodiversity efforts. 



The discovery also highlights how careful observation can reveal new life forms in waters that scientists survey for resource management.



<h2 class="wp-block-heading" id="h-cataloging-eel-species">Cataloging eel species</h2>



The expedition team aboard the research vessel called <a href="https://www.fao.org/newsroom/detail/Norway-and-FAO-launch-unique-state-of-the-art-oceanic-research-ship/en" target="_blank" rel="noreferrer noopener">Dr. Fridtjof Nansen</a> focused on studying fishing resources and ocean life around the <a href="https://nha.org/research/nantucket-history/history-topics/cape-verde-archipelago/" target="_blank" rel="noreferrer noopener">Cabo Verde Archipelago</a>. 



Researchers took samples at varying depths to map habitats and document marine <a href="https://www.earth.com/news/serpent-like-eel-named-after-hades-god-of-the-underworld/">diversity</a>.



Their work included cataloging eels and other underexplored species in the Eastern Central Atlantic. During these trawls, the spoon-nose eel surfaced and initially passed as an already known specimen.



<h2 class="wp-block-heading" id="h-unique-features-of-new-eel-species">Unique features of new eel species</h2>



Closer analysis showed a short, blunt snout, large eyes, and a body length of about 28 inches (0.7 meters). The dorsal fin sits in a slightly advanced position compared to its closest relatives.



“It co-occurs in the tropical eastern Atlantic with two similar looking species,” wrote Dr. Nascimento da Luz. Another trait setting it apart is the arrangement of teeth, which appear fang-like near its pointed head.



<h2 class="wp-block-heading" id="h-a-peek-into-eel-diversity">A peek into eel diversity</h2>



These tooth structures place the eel in the family <a href="https://biogeodb.stri.si.edu/sftep/en/thefishes/taxon/356" target="_blank" rel="noreferrer noopener">Ophichthidae</a>, which is known for species sometimes referred to as worm or snake eels. The family has an array of body shapes, snout types, and feeding strategies.



Scientists found that differences in fin placement and specific head ratios made it clear that this fish deserved its own name. “We have no doubt as to its uniqueness,” stated Dr. Nascimento da Luz, the lead researcher on this project.



<h2 class="wp-block-heading" id="h-clues-from-a-single-specimen">Clues from a single specimen</h2>



Though only one individual has been found, the data collected was surprisingly rich. 



Scientists used detailed morphometrics, measuring things like fin position, head-to-body ratio, and tooth shape, to distinguish it from known relatives.



DNA analysis added another layer of certainty. Researchers found a 3.6% genetic difference from its closest cousin, Mystriophis crosnieri, enough to classify it as a separate species.



<h2 class="wp-block-heading" id="h-why-spoon-nose-eel-species-matter">Why spoon-nose eel species matter</h2>



Spoon-nose <a href="https://www.earth.com/news/sushi-of-the-future-the-first-ever-lab-grown-eel-is-a-success/">eels</a> help researchers understand how fish evolve in deep-sea environments where visibility is low and prey is scarce. Their body shape, hunting tools, and fin placement all offer clues to how species adapt over time.



Because they tend to live in deeper waters, they are rarely seen. Each new find adds to the scientific puzzle of how life functions in low-light, high-pressure ecosystems that are still largely unexplored.



<h2 class="wp-block-heading" id="h-local-impact-in-cabo-verde">Local impact in Cabo Verde </h2>



Discoveries like this bring global attention to regions like Cabo Verde, encouraging investment in local marine research and training. 



They can also strengthen partnerships between local scientists and international teams working on conservation.



Increased biodiversity awareness can lead to better protection of vulnerable ecosystems. 



As more species are found in these waters, there’s growing incentive to preserve Carbo Verde habitats before they’re impacted by overfishing or climate shifts.



<h2 class="wp-block-heading" id="h-global-quest-for-new-species">Global quest for new species</h2>



Experts estimate that thousands of organisms are described every year, yet many more wait to be documented. 



This <a href="https://www.earth.com/news/eel-trade-is-pushing-another-species-to-the-brink/">eel</a> underscores how ocean surveys can uncover unexpected finds that broaden our knowledge of marine life.



Researchers named the new species after Cabo Verde to honor the location where it was discovered. Such tributes often highlight the importance of local ecosystems and their protection.



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



The exact habits, diet, and reproduction of the new eel species remain mysteries. The single specimen was enough for analysis of morphology, DNA sequencing, and comparisons with related species.



This discovery prompts a deeper look at the region’s underwater habitats. Further expeditions may reveal whether more spoon-nose <a href="https://www.earth.com/news/electric-eels-have-a-secret-weapon-to-generate-electricity/">eels</a> inhabit neighboring waters or if this new find is actually incredibly rare.



<h2 class="wp-block-heading" id="h-challenges-of-deep-sea-discovery">Challenges of deep-sea discovery</h2>



Finding new species like Mystriophis caboverdensis isn’t easy. Deep-sea trawling requires expensive equipment, <a href="https://www.hi.no/en/hi/news/2021/october/after-being-trapped-in-norway-by-the-pandemic,-dr.-fridtjof-nansen-is-once-again-heading-out-into-the-world" target="_blank" rel="noreferrer noopener">long expeditions</a>, and cooperation between countries and institutions.



Even when a sample is collected, identification can take years. Subtle features must be compared across museum records, and genetic testing depends on funding and lab availability.



The fact that Mystriophis caboverdensis remained unnoticed until now raises questions about how many other species slip through the cracks. Even with decades of ocean exploration, large parts of the sea remain poorly studied.



Scientists say continued investment in <a href="https://www.msc.org/en-au/what-we-are-doing/oceans-at-risk/marine-biodiversity" target="_blank" rel="noreferrer noopener">marine biodiversity</a> research could uncover even more undocumented species. Each new find helps paint a clearer picture of how ecosystems work and how they’re changing.



The study is published in <a href="https://mapress.com/zt/article/view/zootaxa.5632.2.4" target="_blank" rel="noreferrer noopener">Zootaxa</a>.



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Scientists discover a new eel species with fang-like teeth

When scientists on a research vessel off the northwestern coast...

In the waters of Lake Malawi, a single group of fish has evolved into over 800 different species in just a few million years. This rapid and concentrated evolutionary explosion has long puzzled scientists.



Now, researchers have uncovered a powerful genetic mechanism that may explain how such extreme <a href="https://www.earth.com/news/climate-mitigation-strategies-may-be-endangering-biodiversity/" target="_blank" rel="noreferrer noopener">biodiversity</a> can arise so quickly.



A recent study led by scientists from the Universities of <a href="https://www.cam.ac.uk/" target="_blank" rel="noreferrer noopener">Cambridge</a> and <a href="https://www.uantwerpen.be/en/" target="_blank" rel="noreferrer noopener">Antwerp</a> reveals that large chunks of reversed, or “flipped,” DNA in <a href="https://www.earth.com/news/curiosity-of-cichlid-fish-boosts-biodiversity-in-lake-tanganyika/" target="_blank" rel="noreferrer noopener">cichlid fish</a> act like evolutionary accelerators.



These chromosomal inversions preserve key genetic traits across generations and help fish adapt swiftly to new habitats - fueling the formation of new species at remarkable speed.



<h2 class="wp-block-heading" id="h-the-shortcut-in-our-genes">The shortcut in our genes</h2>



“Why are there so many different kinds of animals and plants on Earth?” is a question that has guided evolutionary biology for centuries.



In the case of Malawi’s cichlids, all 800-plus species share a common ancestor. Yet they’ve diversified into everything from algae-grazers to sand-sifters to open-water predators - all within the confines of one lake.



To understand this phenomenon, the researchers examined the genomes of over 1,300 individual cichlids. Some species had flipped DNA sections across five chromosomes - a genetic anomaly called a chromosomal inversion.



“We discovered that, in some species, large chunks of DNA on five chromosomes are flipped - a type of mutation called a chromosomal inversion,” said senior author Hennes Svardal from the University of Antwerp.



Ordinarily, recombination reshuffles <a href="https://www.earth.com/news/oldest-human-dna-ever-found-tells-story-of-lost-branch-on-human-neanderthal-family-tree/" target="_blank" rel="noreferrer noopener">DNA</a> each generation by mixing genetic material from both parents.



But inside these chromosomal inversions, the structure blocks recombination. As a result, organisms inherit linked gene sets together, preserving adaptations that function effectively as a group.



<h2 class="wp-block-heading" id="h-fish-supergenes-lock-in-traits">Fish supergenes lock in traits</h2>



“It’s sort of like a toolbox where all the most useful tools are stuck together, preserving winning genetic combinations that help fish adapt to different environments,” said Moritz Blumer from Cambridge’s Department of Genetics.



These preserved gene clusters, or <a href="https://www.earth.com/news/supergenes-drove-the-rapid-spread-of-common-ragweed/" target="_blank" rel="noreferrer noopener">supergenes</a>, help explain how diverse cichlid fish evolve while sharing the same lake. In sandy lake beds, inversions limit gene mixing, helping preserve each species’ unique adaptations despite a lack of barriers.



The supergenes govern traits essential to survival: vision, hearing, feeding behavior, and more. For instance, fish that live in the lake’s deep waters - some as far down as 655 feet (200 meters) - require specialized vision to navigate dim light.



They also need unique diets to survive in the nutrient-poor depths and physiology to withstand high pressure. Their supergenes lock in those abilities.



<h2 class="wp-block-heading" id="h-supergenes-in-fish-interbreeding">Supergenes in fish interbreeding</h2>



Another advantage of these DNA inversions is that they can transfer wholesale between species when different cichlids <a href="https://www.earth.com/news/28000-year-old-hybrid-child-confirms-interbreeding-between-humans-and-neanderthals/" target="_blank" rel="noreferrer noopener">interbreed</a>. This spreads entire suites of beneficial traits in one stroke.



“When different cichlid species interbred, entire inversions can be passed between them - bringing along key survival traits, like adaptations to specific environments, speeding up the process of evolution,” Blumer said.



This genetic mechanism lets adaptations transfer between species, speeding evolution without needing to evolve traits independently each time.



Researchers found these inversions often act as sex chromosomes, determining whether a fish develops as male or female. Because sex chromosomes drive speciation, this finding adds complexity to how cichlids diversify so rapidly.



<h2 class="wp-block-heading" id="h-going-beyond-fish">Going beyond fish</h2>



“While our study focused on cichlids, chromosomal inversions aren’t unique to them,” said co-senior author Richard Durbin, a professor at Cambridge’s Department of Genetics.



“They’re also found in many other animals - including humans - and are increasingly seen as a key factor in <a href="https://www.earth.com/news/evolution-is-not-as-random-as-we-thought/" target="_blank" rel="noreferrer noopener">evolution</a> and biodiversity.”



These findings reveal new ways to study the genetics of speciation. This applies not just to fish, but across all branches of the tree of life. Supergenes and inversions may be more than just quirks of DNA - they could be among evolution’s most powerful tools for generating new forms and functions.



“We have been studying the process of speciation for a long time,” Svardal said. “By understanding how these supergenes evolve and spread, we’re getting closer to answering one of science’s big questions: how life on Earth becomes so rich and varied.”



The study shows how a DNA twist can speed evolution, offering a key clue to the mystery of biodiversity. It also reveals that sometimes, nature hides its most elegant solutions in its smallest structures.



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Genetic ‘supergenes’ power explosive evolution in some fish

In the waters of Lake Malawi, a single group of...

Mercury levels in Arctic animals keep climbing even though the world has reduced new emissions. A new study shows that mercury already in the ocean is drifting northward on century-long currents and silently refueling pollution.



Researchers from <a href="https://international.au.dk/" target="_blank" rel="noreferrer noopener">Aarhus University</a> and the <a href="https://www.ku.dk/en" target="_blank" rel="noreferrer noopener">University of Copenhagen</a> analyzed more than 700 samples collected across Greenland.



The experts compared modern tissues from <a href="https://www.earth.com/news/international-polar-bear-day-keeping-moms-and-cubs-safe/" target="_blank" rel="noreferrer noopener">polar bears</a>, seals, fish, peat, and even 40-year-old archives, then matched each sample’s six mercury isotopes - slight atomic variants that act like barcodes - to known ocean pathways.



“These isotope signatures act like fingerprints, revealing the sources and transport pathways of mercury,” explained lead author Jens Søndergaard, a senior researcher at Aarhus.



<h2 class="wp-block-heading" id="h-old-emissions-ride-ocean-loops">Old emissions ride ocean loops</h2>



When smokestacks or gold mines release mercury, the vapor can circle the globe for a year before it falls out of the air. Once it sinks into seawater, however, the metal can linger for three hundred years.



The new study shows that this “legacy mercury” is now the main supplier to the Arctic. Water entering central West Greenland rides the North Atlantic’s Irminger Current and arrives with a different isotopic stamp than water feeding the north and east coasts, which drifts down from the Arctic Ocean.



In regions swept by the Atlantic branch, animals carry less total mercury but show higher values of the heavy isotope δ202Hg. Farther north and east, concentrations are higher and the isotope mix points to older Arctic stores.



<h2 class="wp-block-heading" id="h-mercury-climbs-in-arctic-predators">Mercury climbs in Arctic predators</h2>



Scientists have tracked Arctic mercury since the late 1970s, hoping to see a decline after many countries ratcheted down pollution.



Instead, concentrations in polar bears and <a href="https://www.earth.com/news/newly-discovered-species-of-toothed-whale-is-the-earliest-ancestor-of-modern-dolphins/" target="_blank" rel="noreferrer noopener">toothed whales</a> are now twenty- to thirtyfold above pre-industrial levels.



“We’ve monitored mercury in Arctic animals for over 40 years. Despite declining global emissions since the 1970s, we see no corresponding decrease in Arctic concentrations - on the contrary,” said senior author Rune Dietz, an ecologist at Aarhus.



The new isotope data show why: mercury carried by currents can take up to a century and a half to reach Greenland.



<h2 class="wp-block-heading" id="h-isotopes-trace-mercury-s-path">Isotopes trace mercury's path</h2>



Mercury atoms come in several naturally occurring forms that differ slightly in mass. Industrial smokestacks, volcanic plumes, rivers, and ocean chemistry each leave a characteristic mix.



By scanning these mixes in muscle, fur, and ancient peat layers, the team drew a map of hidden routes. In central West Greenland the isotope blend matches Atlantic inflow; in north-eastern sites it matches the high-mercury Arctic Basin.



The peat cores also tell a time-lapse story: layers laid down in recent centuries hold heavier isotopes than layers deeper in the <a href="https://www.earth.com/news/permafrost-thaw-is-a-rising-threat-to-arctic-communities/" target="_blank" rel="noreferrer noopener">permafrost</a>, confirming that modern pollution is still piling up.



<h2 class="wp-block-heading" id="h-health-impacts-of-mercury">Health impacts of mercury</h2>



“Mercury affects the immune system, reproduction, and possibly sensory functions in animals, which can impact their survival,” said co-author Christian Sonne, a professor at Aarhus.



Seals, polar bears, and seabirds already harbor levels linked to suppressed immunity and hormonal disruption. 



Indigenous communities that rely on marine mammals for food face the same toxic threat. With mercury reservoirs still drifting north, even the toughest emission cuts may not deliver quick relief.



<h2 class="wp-block-heading" id="h-arctic-slow-to-reflect-progress">Arctic slow to reflect progress</h2>



The <a href="https://minamataconvention.org/en" target="_blank" rel="noreferrer noopener">United Nations Minamata Convention</a> aims to curb new mercury emissions. The Danish team’s work explains why Arctic numbers refuse to fall despite progress elsewhere.



Ocean inventories of legacy mercury - much of it released during the 19th- and 20th-century coal age - are simply too vast and too slow-moving. Any evaluation of the treaty’s success, the authors warn, must account for that time lag.



The group is expanding its isotope surveys through the <a href="https://www.earth.com/news/microbial-awakening-arctic-food-webs-are-transforming-from-green-to-brown/" target="_blank" rel="noreferrer noopener">GreenPaths project</a> and collaborating with international programs such as WhaleAdapt to follow mercury’s course through other <a href="https://www.earth.com/news/microbial-awakening-arctic-food-webs-are-transforming-from-green-to-brown/">Arctic food webs</a>.



By stitching together isotope records from peat, glaciers, rivers, and marine life, they hope to predict hotspots years before the pollutant arrives.



<h2 class="wp-block-heading" id="h-what-can-be-done-now"><a></a>What can be done now?</h2>



Reducing modern mercury still matters; every gram kept out of the water is one less gram entering the conveyor belt.



But policymakers must pair emission goals with long-term monitoring, dietary guidance for northern communities, and studies on how climate-driven shifts in currents could speed or slow the toxic flow.



The lesson is stark: once mercury reaches the sea, it becomes a traveler with no passport expiry. And as the new isotope “fingerprints” show, the <a href="https://www.earth.com/news/forever-chemicals-threaten-arctic-wildlife-and-human-health/" target="_blank" rel="noreferrer noopener">Arctic’s wildlife</a> - and the people who depend on it - will keep feeling the aftershocks of 19th- and 20th-century pollution well into the 22nd.



The study is published in the journal <a href="https://www.nature.com/articles/s41467-025-60356-6" target="_blank" rel="noreferrer noopener">Nature Communications</a>.



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Mercury pollution rides ocean currents north, threatening Arctic wildlife

Mercury levels in Arctic animals keep climbing even though the...

The Karoo stretches across more than 150,000 square miles of semi-arid South Africa, a place where sun-bleached soil keeps secrets older than dinosaurs. Wander its stony flats and you’ll see ridges of exposed rock that look like the pages of a giant book. 



The “chapters” span hundreds of millions of years, each one packed with fossilized bone and impressions of vanished forests. For anyone fascinated by life’s backstory, the Karoo is irresistible.



Long before geology students arrived with measuring tapes and plaster, Indigenous families lived among those same outcrops. 



The San, sometimes called the /Xam, camped at waterholes, painted hunting scenes on sandstone walls, and passed down tales of shape-shifting serpents that brewed thunderstorms. 



Their art survives in shallow caves and overhangs, capturing the everyday and the uncanny with equal care.



<h2 class="wp-block-heading" id="h-dicynodont-art-painted-in-caves">Dicynodont art painted in caves</h2>



The Karoo’s fossil fame rests on creatures named dicynodonts - chunky plant-eaters about the size of pigs, sporting a beak and two downward-pointing tusks. 



They ruled the Permian Period more than 250 million years ago, well before the <a href="https://www.earth.com/news/where-did-dinosaurs-come-from-missing-fossils-hold-the-secret/" target="_blank" rel="noreferrer noopener">first dinosaur hatched</a>. 



Because the region is dry and wind-scoured, dicynodont skulls often erode straight out of hillsides; a passerby can spot the ivory-colored bone from yards away. 



It’s not hard to imagine early herders stumbling upon those skulls and weaving them into local lore.



<a href="https://en.wikipedia.org/wiki/San_people" target="_blank" rel="noreferrer noopener">The San</a> also left thousands of charcoal and ochre paintings. Some show antelope and giraffes, others depict trance dances where healers slip into the spirit world. 



Among the most intriguing images appears on a wall known as the Horned Serpent panel, created between 1821 and 1835. 



One painted figure stretches like a slender <a href="https://www.earth.com/news/crocodile-evolution-was-influenced-by-environmental-factors/" target="_blank" rel="noreferrer noopener">crocodile</a> but displays a pair of tusks that bend toward the ground - no living African animal matches that appearance.



<h2 class="wp-block-heading" id="h-tusks-on-the-rock-wall">Tusks on the rock wall</h2>



When researchers first cataloged the panel, they guessed the creature might be a rain-making spirit. That interpretation fit San cosmology, where serpents often control clouds. 



Yet even a mythic animal usually borrows details from reality: hoof shapes, horn curls, or in this case, tusks. The puzzle lingered for decades.



A fresh investigation recently took a different angle. 



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/06/cave-art_south-africa_1800s_dicynodont-extinct_credit-Julien-Benoit_1big.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/06/cave-art_south-africa_1800s_dicynodont-extinct_credit-Julien-Benoit_1s.webp" alt="Painting of the dicynodont made by the San in the early 1800s. Credit: Julien Benoit" class="wp-image-1973469"/></a><figcaption class="wp-element-caption">Painting of the dicynodont made by the San in the early 1800s. Click image to enlarge. Credit: Julien Benoit</figcaption></figure>



After carefully comparing the painted outline with dozens of Karoo fossils, a paleontologist noticed striking overlap - head shape, tusk angle, and body proportions mirrored those of a typical <a href="https://www.earth.com/news/gordonia-traquairi-pig-like-creature-discovered-roamed-earth-250-million-years-ago/" target="_blank" rel="noreferrer noopener">dicynodont skeleton</a>. 



The artist seems to have sketched what looks like a fossil skull still embedded in rock, then fused it with a serpent’s sinuous torso.



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



The idea gains strength from archaeology. Dig sites near San shelters have yielded chipped stone tools alongside fossil fragments carried from distant outcrops. 



That means people collected ancient bones, perhaps as curios or ritual objects. 



Oral traditions recorded in the late 1800s even speak of colossal beasts that once walked the land before “the ground dried and cracked.” Those tales echo the fossil record’s story of extinction during the end-Permian mass die-off.



If the cave art painting really captures a dicynodont, it predates formal paleontology. Western science first named a species in 1845, yet the Horned Serpent panel was finished no later than 1835. 



<figure class="wp-block-image aligncenter size-full"><img src="https://www.earth.com/wp-content/uploads/2025/06/cave-art_south-africa_1800s_dicynodont_horned-serpent-panel_credit-Julien-Benoit_1s.webp" alt="The Horned Serpent panel. A, general view of the Horned Serpent panel photographed in 2024 by the author. B, close up of the section figured in Stow and Bleek's plate 39. C, close up of the tusked animal. D, close up of the warriors painted below the Horned Serpent panel. E, close up of the warriors painted to the right of the panel. Credit: Julien Benoit, 2024, PLOS ONE" class="wp-image-1973466"/><figcaption class="wp-element-caption">The Horned Serpent panel. A, general view of the Horned Serpent panel photographed in 2024 by the author. B, close up of the section figured in Stow and Bleek's plate 39. C, close up of the tusked animal. D, close up of the warriors painted below the Horned Serpent panel. E, close up of the warriors painted to the right of the panel. Click image to enlarge. Credit: Julien Benoit, 2024, PLOS ONE</figcaption></figure>



“The painting was made in 1835 at the latest, which means this dicynodont was depicted at least ten years before the western scientific discovery and naming of the first dicynodont by Richard Owen in 1845," noted Julien Benoit of the <a href="https://www.wits.ac.za/" target="_blank" rel="noreferrer noopener">University of the Witwatersrand</a>, author of this study. 



"This work supports [the fact] that the first inhabitants of southern Africa, the San hunter-gatherers, discovered fossils, interpreted them and integrated them in their rock art and belief system.”



<h2 class="wp-block-heading" id="h-deciphering-the-dicynodont-art">Deciphering the dicynodont art</h2>



Benoit and colleagues photographed the panel under varying light, traced outlines digitally, and matched them with museum specimens. 



The correlation, they argue, is too tight to be chance. Their work joins a handful of cases worldwide - China, Australia, North America - where Indigenous art may double as the earliest depiction of extinct animals.



The research also nudges scientists to widen their lens. Fossil discovery stories often center on explorers in pith helmets, but communities living alongside outcrops have noticed, collected, and wondered about old bones for millennia. 



Recognizing that legacy broadens the history of paleontology and honors knowledge systems that predate universities.



<h2 class="wp-block-heading" id="h-why-does-any-of-this-matter">Why does any of this matter?</h2>



Beyond scholarly credit, the find invites fresh partnerships. Rock art sites need protection from erosion, vandalism, and mining. 



By linking paintings to fossils, heritage managers can argue for preserving whole landscapes rather than isolated walls. That approach safeguards both <a href="https://www.earth.com/news/children-played-a-spiritual-role-in-prehistoric-cave-art/" target="_blank" rel="noreferrer noopener">cultural memory</a> and the deep-time record locked in nearby strata.



The study also sparks questions for educators. Imagine guiding school groups to a shelter where a dicynodont skull rests at the foot of a painted serpent. 



Students could trace a line from 250-million-year-old mud to a 19th-century brushstroke, then to modern CT scans revealing bone microstructure. 



Such encounters make earth science tangible and show that curiosity about ancient life is a shared human trait, not an imported discipline.



<h2 class="wp-block-heading" id="h-how-is-this-dicynodont-art-possible">How is this dicynodont art possible?</h2>



Evidence that the San looked at fossils and painted what they saw does more than solve an art mystery. It stitches together culture, geology, and memory across staggering spans of time. 



In the Karoo, one can touch Triassic bone, read a 19th-century pigment trail, and hear present-day scholars debating both. Each element enriches the others. 



The Horned Serpent panel stands as a quiet reminder that the urge to understand our planet’s past didn’t begin in lecture halls - it began wherever someone knelt beside a curious rock and started to wonder.



The full study was published in the journal <a href="https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0309908" target="_blank" rel="noreferrer noopener">PLOS One</a>.



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Cave art discovery depicts an animal that went extinct 280-million-years ago, baffling scientists

The Karoo stretches across more than 150,000 square miles of...

A herd of mastodons, rhinoceroses, and giant deer once roamed freely across Earth. Their lives shaped landscapes for tens of millions of years. In a sweeping new study, scientists examined fossil records from more than 3,000 large herbivores to see how their world shifted, and how it didn’t.



An international team of researchers led by Fernando Blanco at the <a href="https://www.gu.se/" target="_blank" rel="noreferrer noopener">University of Gothenburg</a> discovered that herbivore <a href="https://www.earth.com/news/large-herbivore-extinctions-drastically-affect-forest-ecosystems/" target="_blank" rel="noreferrer noopener">ecosystems</a> remained surprisingly steady for long stretches. But they also pinpointed two pivotal moments where the balance flipped.



<h2 class="wp-block-heading" id="h-herbivores-shifted-during-climate-change">Herbivores shifted during climate change</h2>



The first ripple hit around 21 million years ago. A land bridge emerged as the ancient Tethys Sea closed. Suddenly, elephants and relatives could walk from Africa into Eurasia. Other hoofed animals, deer, pigs, rhinos, joined them.&nbsp;



“The environmental pressure was so great that the entire system underwent global reorganization,” noted Blanco. At this point, hoofed communities didn’t collapse, they reassembled. 



Larger brows­ing species with mid‑to‑high crowned molars became dominant. Network analyses of those fossil data reveal a shift to a new <a href="https://www.earth.com/news/animals-with-high-body-temperatures-often-become-herbivores/" target="_blank" rel="noreferrer noopener">system</a> across continents, the first major global transformation in herbivore functional types.



Roughly ten million years later, another reinvention unfolded, this time silently. A cooling, drying climate expanded grasslands worldwide. Forest‑dwelling browsers declined. Grazers equipped with tougher teeth spread.



A functional tipping point followed, reshaping the roles of herbivores again. Grazers and mixed feeders dominated, equipped with both high‑ and low‑crowned teeth. From then on, functional diversity began a long decline, a trend scientists trace onward through the <a href="https://ucmp.berkeley.edu/quaternary/ple.html" target="_blank" rel="noreferrer noopener">Pleistocene</a> and beyond.



<h2 class="wp-block-heading" id="h-different-species-same-ecosystem-structure">Different species, same ecosystem structure</h2>



“It’s like a football team changing players during a match but still keeping the same formation. Different species came into play but they fulfilled similar ecological roles, so the overall structure remained the same,” explained Ignacio A. Lazagabaster of CENIEH in Spain. 



Despite these transformations, the ecosystem backbone remained intact. Even as mastodons, woolly mammoths, and giant rhinos disappeared in the last 129,000 years, the roles they played weren’t lost. 



The network models show that after these extinctions, community configurations, known as continental functional faunas, remained remarkably consistent.



That consistency holds through the last 4.5 million years, reflecting resilience through ice ages and environmental upheavals. Still, the team warns that modern <a href="https://www.earth.com/news/tricking-animals-with-odor-could-save-plants-from-browsing-damage/" target="_blank" rel="noreferrer noopener">biodiversity</a> loss is happening much faster - and could trigger a third tipping point before ecosystems can adjust.



<h2 class="wp-block-heading" id="h-why-these-transitions-matter-now">Why these transitions matter now</h2>



Functional diversity began declining around 10 million years ago, during the spread of C4 grasses and shrinking forests. As herbivores with specialized teeth rose to dominance, the global count of functional roles dropped by about 65 percent in roughly 5 million years.&nbsp;



The drop intensified around 2.5 million years ago with glacial cycles and major biotic exchanges, like <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC2987556/" target="_blank" rel="noreferrer noopener">the Great American Interchange</a>.



Still, the overall shape of ecosystems held firm. The continents shared similar functional configurations even as roles vanished. But today, the authors caution, biodiversity is receding much faster. They warn that another irreversible reorganization may soon be triggered.



<h2 class="wp-block-heading" id="h-herbivores-and-modern-changes">Herbivores and modern changes</h2>



<a href="https://stri.si.edu/story/hungry-megaherbivores" target="_blank" rel="noreferrer noopener">Megaherbivores</a>, those weighing more than a ton, have largely vanished. <a href="https://www.britannica.com/animal/proboscidean" target="_blank" rel="noreferrer noopener">Proboscideans</a>, which once numbered up to 33 species, now survive as just a handful. Yet scientists estimate that they comprised only about 15-18 percent of functional types in most regions. Their loss reduces ecosystem richness but didn’t break the system.



“We may soon reach a third global tipping point, one that we’re helping to accelerate,” said Juan L. Cantalapiedra of Spain’s <a href="https://www.mncn.csic.es/es" target="_blank" rel="noreferrer noopener">MNCN</a>.



The study highlights the importance of large herbivores in ecosystem function. Conservation efforts that protect or reintroduce them could help restore key ecological roles lost in recent millennia.



<h2 class="wp-block-heading" id="h-signals-from-the-fossil-record">Signals from the fossil record</h2>



The fossil record offers a rare, long-term perspective on ecological resilience. By tracking traits like <a href="https://www.sciencedirect.com/science/article/pii/S1349007922000895" target="_blank" rel="noreferrer noopener">tooth morphology</a> and body size across thousands of extinct herbivores, the researchers built a detailed picture of how animals responded to shifting <a href="https://www.earth.com/news/arctic-grazers-secretly-shape-plant-growth-and-survival/" target="_blank" rel="noreferrer noopener">environments</a> over time. 



The team's data-driven approach captured how new species stepped into familiar roles, even after dramatic losses. The research reveals a disconnect between species loss and system collapse. 



While many individual species disappeared, their ecological roles often lived on through new players. That buffering capacity is what kept herbivore ecosystems functionally stable for 60 million years. The question now is whether that same resilience can hold under today’s faster pace of change.



<h2 class="wp-block-heading" id="h-protecting-the-roles-of-herbivores">Protecting the roles of herbivores</h2>



Ancient ecosystem changes took thousands to millions of years to unfold. Humans are transforming biodiversity on century scales. This study shows that large herbivore communities can adapt to change - but only up to a point.



If current declines continue, we risk triggering a shift beyond recovery. Protecting the functional diversity of herbivores is as crucial as protecting population numbers. 



Restoring or preserving herbivore populations may help systems stay resilient as conditions continue to change.



The study is published in the journal <a href="https://www.nature.com/articles/s41467-025-59974-x" target="_blank" rel="noreferrer noopener">Nature Communications</a>.



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Herbivores survived millions of years of change - but now face a modern crisis

A herd of mastodons, rhinoceroses, and giant deer once roamed...

A year-long experiment on a Central Valley dairy farm has confirmed that sealing manure lagoons under gas-tight tarps can trap roughly 80 percent of the methane they would otherwise release.



By capturing the gas and sending it to fuel markets, the system turns a potent climate threat into a usable resource.



Led by researchers from the <a href="https://www.ucr.edu/" target="_blank" rel="noreferrer noopener">University of California, Riverside</a> (UCR), the study gives the first independent, year-over-year check on dairy “digesters” that California regulators have counted on to meet aggressive methane-cutting goals.



More than 130 such systems already dot the state’s milk belt. Until now, officials had relied mainly on engineering models to judge their effectiveness.



<h2 class="wp-block-heading" id="h-capturing-methane-gas-on-a-dairy-farm">Capturing methane gas on a dairy farm</h2>



The test site sits in Tulare County, the nation’s top milk-producing region. Hot summers keep open manure ponds bubbling like low-grade cauldrons, releasing <a href="https://www.earth.com/news/how-ai-can-help-reduce-methane-emissions-from-cows/" target="_blank" rel="noreferrer noopener">methane</a> that warms the planet more than 80 times faster than carbon dioxide over two decades.



Engineers solved the problem by floating a heavy, flexible cover across the lagoon and piping the captured gas through scrubbers before sending it to truck fleets as a low-carbon diesel replacement.



“The digesters can leak, and they sometimes do,” said Francesca Hopkins, the UCR climate scientist who led the work. “But when the system is built well and managed carefully, the emissions really drop. That’s what we saw here.”



<h2 class="wp-block-heading" id="h-measuring-the-invisible"><a></a>Measuring the invisible</h2>



Hopkins’ team set up mobile gas analyzers inside a white research van. For 12 months before construction and twelve months after, they drove grid patterns around the dairy, logging hundreds of methane readings under different winds and <a href="https://www.earth.com/news/arctic-warming-fuels-dangerous-methane-feedback-loop/" target="_blank" rel="noreferrer noopener">temperatures</a>.



The before-and-after comparison showed an 80 percent decline in methane drifting off the property once the cover and piping were in place.



That figure lines up closely with the reduction assumed in California’s official climate inventory.



Most earlier studies had relied on short snapshots or on-site sensors. The new roaming approach captured seasonal swings, day-night cycles, and operational hiccups, providing a more realistic picture of performance over time.



<h2 class="wp-block-heading" id="h-leaks-fixes-and-fast-improvements"><a></a>Leaks, fixes, and fast improvements</h2>



During early tests the team picked up sudden methane spikes. They alerted <a href="https://calbioenergy.com/" target="_blank" rel="noreferrer noopener">California Bioenergy</a>, the company that built and operates the digester. Technicians located torn seams and loose joints, repaired them, and the plumes vanished on subsequent drives.



“This was a textbook case of adaptive management,” Hopkins said. “The partnership between scientists, the company, and the farmer really made a huge difference.”



The episode underlines a broader lesson: digesters work best when operators monitor them closely and move quickly to plug leaks.



California’s new fleet of methane-tracking satellites could help, flagging large plumes so ground crews can respond in days instead of months.



<h2 class="wp-block-heading" id="h-other-pollutants-remain-untouched">Other pollutants remain untouched</h2>



Digesters leave other pollution untouched. They do not curb <a href="https://www.earth.com/news/new-green-tech-ammonia-fertilizer-production-using-earths-natural-forces/" target="_blank" rel="noreferrer noopener">ammonia</a>, a lung-irritating gas, or tiny airborne particles that can hang over dairy counties on still summer days. 



The hardware is also expensive. Farmers need permits, financing, and maintenance contracts to keep covers inflated and engines running.



“They’re not for every farm,” Hopkins said. “But for dairies that can make it work, this is one of the most cost-effective ways we have to cut these <a href="https://www.earth.com/news/2023-climate-change-report-record-high-temperatures-greenhouse-gases-sea-level-rise/" target="_blank" rel="noreferrer noopener">greenhouse gas emissions</a>.”



California’s climate program helps in this regard by awarding low-carbon fuel credits for each ton of methane kept out of the air. Those credits, sold to oil companies that need to hit clean-fuel targets, can repay installation costs in a few years.



<h2 class="wp-block-heading" id="h-slashing-methane-emissions-from-dairy-farms">Slashing methane emissions from dairy farms</h2>



State agencies plan to slash dairy methane 40 percent below 2013 levels by 2030. The new study suggests that target remains within reach if existing digesters keep performing and more come online. 



The research also shows that rigorous, transparent monitoring can build confidence among regulators, industry, and local communities.



“There’s so much division in the climate space,” Hopkins said. “But this is a real example of cooperation that leads to measurable results.”



Digesters will not solve every problem tied to large-scale dairying, yet the Tulare County project proves they can deliver the climate benefit promised on their labels.



With careful design, vigilant upkeep, and open data, farms can turn what was once a methane plume into fuel for trucks, revenue for operators, and progress toward a lower-carbon future.



The study is published in the journal <a href="https://onlinelibrary.wiley.com/doi/10.1111/gcbb.70047">Global Change Biology Bioenergy</a>.



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Dairy farms can join the climate fight by trapping methane

A year-long experiment on a Central Valley dairy farm has...

Researchers have launched a database that tracks the maximum body size of over 85,000 marine animal species. This resource spans creatures from tiny zooplankton to massive whales.



“Put simply, biologists have tended to focus on bigger organisms. And as a result, a lot of our understanding of how marine food webs and ecosystems work is based on knowledge of these larger <a href="https://www.earth.com/news/how-ocean-animals-connect-countries-and-continents/" target="_blank" rel="noreferrer noopener">species</a>,” said study co-author Dr. Tom Webb from the <a href="https://www.sheffield.ac.uk/" target="_blank" rel="noreferrer noopener">University of Sheffield</a>.



For decades, marine science has placed the most emphasis on large species. Now, smaller species are getting some attention. Including them matters because they make up most of marine biodiversity and play vital ecosystem roles.



<h2 class="wp-block-heading" id="h-why-size-matters-in-marine-species">Why size matters in marine species</h2>



Body size shapes how ocean creatures live and interact. It influences where they feed, how they move, and their chances of surviving environmental <a href="https://www.earth.com/news/world-oceans-day-2025-sustaining-what-sustains-us/" target="_blank" rel="noreferrer noopener">changes</a>.



Research confirms that size patterns help predict the ecological impact of marine species. Studies show ecosystems are organized by size, with bigger animals eating smaller ones.



Missing size data has hindered climate and conservation models. With 40% of marine species now included, scientists can make stronger predictions. They expect coverage to rise to 75% in the next two years.



The project is led by Dr. Craig R. McClain at the <a href="https://louisiana.edu/" target="_blank" rel="noreferrer noopener">University of Louisiana</a>, working with experts from Sheffield, Tufts, Stanford, Hawaiʻi, and Virginia Tech.



“Body size isn’t just a number - it’s a key to how life works,” said Professor McClain. "This database fills a critical information gap and offers a fresh perspective on ocean biodiversity."



<h2 class="wp-block-heading" id="h-how-tech-helped-gather-size-data">How tech helped gather size data</h2>



The creation of MOBS relied on automated data mining tools that pulled species measurements from thousands of publications and records.



Advances in machine learning helped standardize inconsistent formats and reduce manual entry time.



The researchers also used global taxonomy systems like <a href="https://www.marinespecies.org/about.php" target="_blank" rel="noreferrer noopener">WoRMS</a> to verify species names and classifications. This integration ensured that their data could be reliably linked with other major marine datasets.



<h2 class="wp-block-heading" id="h-a-massive-marine-dataset">A massive marine dataset</h2>



Known as <a href="https://onlinelibrary.wiley.com/doi/10.1111/geb.70062" target="_blank" rel="noreferrer noopener">MOBS</a> (Marine Organismal Body Size Database), it records maximum measures like length, width, and height - standardized across 30 marine animal phyla. The initial release includes 85,204 species and over 181,000 size entries.



The data draws from scientific literature, museum records, and online repositories. It’s open source and freely available through <a href="https://github.com/crmcclain/MOBS_OPEN" target="_blank" rel="noreferrer noopener">GitHub</a>.



With size data spanning tens of thousands of species, scientists can now explore how body size evolved across different lineages. 



They can test long-standing theories about how environmental pressures, such as ocean depth or temperature, shaped the evolution of size in marine animals.



The database also enables comparisons between extinct and living species. By integrating fossil records, researchers can trace size shifts over time and investigate extinction patterns related to body size across evolutionary history.



<h2 class="wp-block-heading" id="h-smaller-species-bigger-blind-spots">Smaller species, bigger blind spots</h2>



Scientists are already using MOBS to explore biases in <a href="https://www.earth.com/news/national-dolphin-day-2025-honoring-the-oceans-most-playful-minds/" target="_blank" rel="noreferrer noopener">species</a> documentation. Smaller marine species often get overlooked in biodiversity surveys, raising questions about conservation priorities.



Researchers are also analyzing how body size changes with climate shifts. Since size affects metabolism and vulnerability, this insight is critical for forecasting ecosystem responses.



This database has real-world implications. Fishing large species disrupts food webs, and those effects ripple down to smaller prey.



Now models can account for these interactions accurately. Insights from birds show larger species face higher extinction risk. A robust marine size dataset may reveal similar trends, improving risk assessment and policy interventions.



<h2 class="wp-block-heading" id="h-protecting-small-vulnerable-species">Protecting small, vulnerable species</h2>



Policymakers and fisheries managers can use size data from MOBS to better regulate marine harvests. Knowing the size structure of species helps design catch limits that maintain ecological balance and prevent overexploitation.



The database also supports marine spatial planning. Regions with high concentrations of small or vulnerable species can be prioritized for conservation zones, improving how resources are allocated for ocean protection.



The project aims to integrate with <a href="https://obis.org/" target="_blank" rel="noreferrer noopener">OBIS</a> (Ocean Biodiversity Information System) and other marine data platforms, enabling spatial and ecological mapping.



With open-source access, the database invites global contributions. Scientists worldwide can suggest updates, correct errors, and share measurements, promoting a community-based science model.



<h2 class="wp-block-heading" id="h-marine-education-and-citizen-science">Marine education and citizen science</h2>



The open-access nature of the MOBS database also opens doors for educators and citizen scientists. Teachers can use real species data in classrooms to introduce students to marine biology, ecology, and data science.



Citizen science groups can incorporate the database into biodiversity monitoring projects. Having access to maximum body size info helps with field identification, ecosystem modeling, and community-led marine conservation initiatives.



<a href="https://www.earth.com/news/sand-extraction-is-an-overlooked-threat-to-marine-ecosystems/" target="_blank" rel="noreferrer noopener">Ocean ecosystems</a> face mounting stress. Climate change, overfishing, and habitat damage threaten marine life.



This dataset gives conservationists better tools to understand and protect ocean biodiversity. By grounding strategies in data that span tiny plankton to whales, MOBS bridges ecological gaps and supports stronger conservation efforts.



The study is published in the journal <a href="https://onlinelibrary.wiley.com/doi/10.1111/geb.70062" target="_blank" rel="noreferrer noopener">Global Ecology and Biogeography</a>.



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Body size of 85,000 marine species mapped in new database

Researchers have launched a database that tracks the maximum body...

Measuring around 1 inch in length with a wingspan of approximately 2.7 inches, an ancient cicada <a href="https://www.earth.com/news/fossil-discovery-pushes-back-reptile-evolution-by-40-million-years/">fossil</a> has captured attention for preserving detailed wing veins. Researchers suggest it was part of a family of “true” singing <a href="https://www.nature.org/en-us/get-involved/how-to-help/animals-we-protect/what-to-know-about-brood-x-cicadas/">cicadas</a> that are still common across many warm regions today.



Experts were intrigued by the fossil’s nearly complete form. Its wings, pressed against stone, showed patterns seldom seen in insects so old. 



<h2 class="wp-block-heading" id="h-how-the-cicada-fossil-was-found">How the cicada fossil was found</h2>



The study was led by <a href="https://www.researchgate.net/scientific-contributions/Hui-Jiang-2134327699" target="_blank" rel="noreferrer noopener">Dr. Hui Jiang</a> at the <a href="https://www.uni-bonn.de/en/home" target="_blank" rel="noreferrer noopener">University of Bonn</a> in Germany.



Their team examined layers of rock at the <a href="https://whc.unesco.org/en/list/720/" target="_blank" rel="noreferrer noopener">Messel Pit</a> in Germany. This site is famous for producing remarkable fossils of birds, mammals, and insects.



Scientists say the rocks where the insect was found date to about 47 million years ago. They report that the cicada’s wings and body were flattened in the sediment, leaving behind fine details.



<h2 class="wp-block-heading" id="h-connecting-to-an-older-lineage">Connecting to an older lineage</h2>



Researchers identified this fossil as part of the tribe <a href="https://www.inaturalist.org/taxa/335506-Platypleurini" target="_blank" rel="noreferrer noopener">Platypleurini</a>, which usually thrives in tropical and subtropical regions across Africa and Asia. 



The presence of this group in ancient Europe challenges previous ideas about how these insects were distributed.



Some investigators think this newly described species, Eoplatypleura messelensis, shared characteristics with modern relatives that sing loudly during summer. That links its lineage to cicadas found in similar climates where humidity and warmth are typical.



“We can’t know the exact song,” said Dr. Hui Jiang. His team proposes the ancient cicada likely produced sounds using <a href="https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/tymbal" target="_blank" rel="noreferrer noopener">tymbals</a>, structures that vibrate to create loud calls.



Because the fossil’s body appears a bit broader than most living cicadas, the males (though not found in these particular specimens) might have produced especially powerful tones. It is possible they reached volumes as high as today’s species or even beyond.



<h2 class="wp-block-heading" id="h-cicada-fossil-was-in-a-volcanic-lake">Cicada fossil was in a volcanic lake</h2>



Scientists explain that an ancient volcanic lake once covered the Messel Pit. Its lower layers had very low oxygen levels, which helped preserve organic material without rapid decay.



Sediments in the lake bed were so fine that delicate features, including wing veins, could fossilize. Research teams have uncovered many insects here, yet this cicada stands out for its intact body and wings.



Prior to this find, the earliest recognized members of this singing-cicada family were traced to other regions tens of millions of years ago. 



This fossil’s age adjusts the timeline for when these creatures established themselves outside Africa and Asia.



“Such discoveries would assist in providing better calibrations for determining a more realistic evolutionary rate,” said <a href="https://naturalhistory.si.edu/staff/conrad-labandeira" target="_blank" rel="noreferrer noopener">Dr. Conrad Labandeira</a> from the <a href="https://naturalhistory.si.edu/" target="_blank" rel="noreferrer noopener">Smithsonian Museum of Natural History</a>. That might reshape estimates of when and where these insects roamed.



<h2 class="wp-block-heading" id="h-filling-evolutionary-gaps">Filling evolutionary gaps</h2>



The <a href="https://www.earth.com/news/tooth-enamel-analysis-suggests-early-eurasians-were-multiple-species-paranthropus-robustus/">fossil</a> record for cicadas is surprisingly limited considering how widespread and noisy they are today. 



Only 44 confirmed Cicadidae fossils have been documented, making each new discovery a valuable puzzle piece for tracing their origins.



Fossils like Eoplatypleura messelensis serve as time markers for refining evolutionary trees. They help researchers test models built from molecular data and revise estimates about when key traits (like singing) first appeared.



Modern cicadas in the Platypleurini tribe often dwell in lush forests and shrubby regions with abundant moisture. The Messel region during the Eocene likely had a warm, humid climate, making it a suitable home for this insect.



By comparing wing structure and overall morphology, researchers suggest Eoplatypleura messelensis belonged to a group that probably relied on strong flight. 



This flight, combined with its potential for loud calls, would have helped it find mates and avoid predators in a dense forest canopy.



<h2 class="wp-block-heading" id="h-modern-cicada-cousins">Modern cicada cousins</h2>



One modern relative, the African cicada <a href="https://entnemdept.ufl.edu/walker/ufbir/chapters/chapter_24.shtml" target="_blank" rel="noreferrer noopener">Brevisana brevis</a>, reaches almost 107 decibels. That is close to a jet taking off. In eastern North America, periodical cicadas often reach 90 to 100 decibels, which is about the roar of a subway.



Next year, <a href="https://cicadas.uconn.edu/broods/brood_14/" target="_blank" rel="noreferrer noopener">Brood XIV</a> will emerge in the eastern United States. Its members appear every 17 years in billions, stirring excitement among enthusiasts who gather to witness the spectacle. 



Whether Eoplatypleura messelensis made a similar commotion remains unknown, but the findings hint at a shared ancestry for ear-splitting calls.



<h2 class="wp-block-heading" id="h-shifting-climates-shrinking-ranges">Shifting climates, shrinking ranges</h2>



This Messel Pit cicada might inspire deeper questions about cicada movements across continents. Scientists are eager to find more <a href="https://www.earth.com/news/archaeopteryx-fossil-soft-tissue-flight-evolution-proves-darwin-right/">fossil</a> material that could reveal how these insects adapted through changing climates.



They also hope that additional specimens from Messel will confirm how early European populations compared to their modern kin in Africa and Asia. That information might illuminate how cyclical Earth events influenced cicada journeys over time.



As Earth cooled after the Eocene, the once-humid regions that supported insects like Eoplatypleura messelensis began to dry and cool. 



This shift likely forced many species southward or into extinction, helping explain why today’s Platypleurini are mostly found in tropical zones.



Evidence suggests that ancient Europe supported a much richer variety of Cicadidae species than it does today. The <a href="https://www.earth.com/news/romers-gap-in-the-fossil-record-now-filled-in-with-tetrapod-discovery-westlothiana-lizziae/">fossil</a> record, especially from Messel and other European sites, shows a stark contrast to the low cicada diversity now seen in regions like Germany.



The study is published in <a href="https://www.nature.com/articles/s41598-025-94099-7" target="_blank" rel="noreferrer noopener">Scientific Reports</a>.



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Scientists find a 47-million-year-old cicada fossil that has even preserved the details of its wings

Measuring around 1 inch in length with a wingspan of...

Having itchy skin is a familiar annoyance for some families, and certain children seem to be hit harder than others. Why do these youngsters develop <a href="https://www.nhs.uk/conditions/atopic-eczema/">atopic eczema</a> when their friends do not - especially if they share similar environments?



A research team has been looking into whether a child’s genetic profile influences the risk of eczema. 



After reviewing a set of data involving children from several countries, the experts uncovered hints that a household <a href="https://www.earth.com/news/national-puppy-day-2025-where-happiness-meets-responsibility/" target="_blank" rel="noreferrer noopener">dog</a> might help offset some of the genetic factors behind itchy skin irritation.



Professor Sara Brown from the University of Edinburgh’s <a href="http://The Institute of Genetics and Cancer https://g.co/kgs/DQMJEzs" target="_blank" rel="noreferrer noopener">Institute of Genetics and Cancer</a> and Dr. Marie Standl from <a href="https://www.helmholtz-munich.de/" target="_blank" rel="noreferrer noopener">Helmholtz Munich</a> contributed to this work and brought fresh insight into how these influences might unfold for families everywhere.



<h2 class="wp-block-heading" id="h-understanding-eczema-in-children">Understanding eczema in children</h2>



Eczema involves red, inflamed patches that can be difficult to soothe. This condition arises from a blend of inherited makeup and influences such as early-life bacterial contact or exposure to specific animals. 



Having a family history of dry skin issues does not guarantee a child will develop it, but it raises the odds.



Scientists have wondered why certain kids with a genetic variant live free of symptoms while others encounter a lifetime of creams and lotions. 



Studies from the <a href="https://www.cdc.gov/nchs/products/databriefs/db460.htm#Key_finding" target="_blank" rel="noreferrer noopener">Centers for Disease Control and Prevention</a> note that 7.3% of adults aged 18 and over have eczema.



Experts have long suspected that <a href="https://www.earth.com/news/are-dogs-replacing-children-how-modern-society-is-changing/" target="_blank" rel="noreferrer noopener">dogs</a> might play a protective part for some children, and this new investigation adds support to that theory.



<h2 class="wp-block-heading" id="h-dogs-may-protect-children-from-eczema">Dogs may protect children from eczema</h2>



Families with a pet dog often report that their kids seem to have fewer episodes of skin flare-ups. The researchers wanted to see if this pattern held up at a molecular level. 



They focused on a segment of DNA near the interleukin-7 receptor (<a href="https://pubmed.ncbi.nlm.nih.gov/17660817/" target="_blank" rel="noreferrer noopener">IL-7R</a>), which helps the body regulate immune cells.



“We know that genetic make-up affects a child’s risk of developing eczema and previous studies have shown that owning a pet dog may be protective,” said Professor Brown. 



One part of the study found that children with a slight twist in that gene could sidestep the usual risk for eczema if they had a <a href="https://www.earth.com/news/why-our-relationships-with-dogs-matter-so-much/" target="_blank" rel="noreferrer noopener">dog</a> in their household early in life.&nbsp;



<h2 class="wp-block-heading" id="h-siblings-might-help-reduce-eczema-risk">Siblings might help reduce eczema risk</h2>



Scientists have also noticed that having older brothers or sisters might offer some protection. Observations point to a possible link between exposure to unique bacteria from siblings and a child’s reaction to environmental triggers. 



Further research is needed to confirm how varied bacterial environments influence the genetic component of eczema.



“Not every preventive measure works for everyone, and that’s precisely why gene-environment studies are crucial,” said Dr. Standl. 



Families sometimes consider adding a second child or adopting a <a href="https://www.earth.com/news/dogs-suffer-from-the-january-blues-just-like-humans/" target="_blank" rel="noreferrer noopener">dog</a> to reduce eczema risk. Not every measure works for everyone.&nbsp;



<h2 class="wp-block-heading" id="h-dogs-don-t-work-for-every-eczema-case">Dogs don’t work for every eczema case</h2>



Scientists emphasize that having a dog from day one does not guarantee eczema-free skin. The recent work did not examine the effects of dogs on treating existing cases of eczema. 



Many professionals caution that introducing an animal might irritate symptoms that are already present.



The researchers suggest that contact with dog-related bacteria might shape a child’s immune response in ways that shift how that interleukin-7 receptor behaves. 



Though this gene variation is not the only cause of eczema, it appears to be important in controlling inflammation. Early-life dog exposure could modify that gene’s effect so the skin’s defensive barriers stay in better shape.



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



The latest findings draw primarily from white European participants, prompting calls for more studies in other populations. 



Eczema affects millions of people <a href="https://nationaleczema.org/eczema-facts/" target="_blank" rel="noreferrer noopener">worldwide</a>, including groups with differing genetic backgrounds. A broader pool of participants will help clarify how these discoveries apply to families everywhere.



Parents often wonder if a dog in the home might lower the odds of their child facing red, itchy skin every night. These early results support the idea that dog ownership might help in specific genetic situations. 



More data from a wider range of people will show whether the same pattern exists in other populations.



<h2 class="wp-block-heading" id="h-eczema-genetics-and-the-future">Eczema, genetics, and the future</h2>



Experts continue exploring the interplay between genetic traits and outside factors to better understand why some children develop eczema. They aim to refine the science so parents have straightforward answers about potential lifestyle steps. 



Future work may also investigate whether other pets or environmental exposures shape this immune balance.



The study team believes that continuing to map the roles of various gene variants could open the door to targeted prevention. 



Parents can stay alert to new findings on additional ways to keep a child’s skin barrier strong. They may also want to consult a pediatrician before making major decisions, especially if a youngster already struggles with chronic irritation.



This study is published in the journal <a href="https://onlinelibrary.wiley.com/doi/10.1111/all.16605" target="_blank" rel="noreferrer noopener">Allergy</a>.



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Dogs might protect children from developing this chronic and common condition

Having itchy skin is a familiar annoyance for some families,...

With names like the blue jay and the mallard, birds are among the most familiar wildlife to the general public. Yet bird naming - where the names come from, what they mean - has remained surprisingly underexplored.



A new study offers the most detailed look yet into this world, revealing patterns that stretch from biology to mythology - and even mistaken medieval beliefs.



Researchers from <a href="https://www.nyu.edu/">New York University</a> (NYU) and the <a href="https://nhm.org/">Natural History Museum of Los Angeles County</a> have compiled a massive database of nearly 11,000 English bird names. The findings show that nearly 90 percent are based on physical or ecological traits, while just 11 percent honor people.



The project is one of the first to quantify the structure and sources behind bird naming. It comes at a time when ornithology is reexamining how these names shape public understanding and whose stories they preserve.



<h2 class="wp-block-heading" id="h-a-comprehensive-naming-atlas"><a></a>A comprehensive naming atlas</h2>



Erin Morrison is a professor in Liberal Studies at NYU and is co-lead author of the study. "Until this database, there was no quantitative way to analyze the current state of terms in English bird names,” she said. 



“In addition to showing that a very small percentage of <a href="https://www.earth.com/news/all-birds-one-tree-complete-evolutionary-map-reveals-hidden-links/">birds</a> are named after people, the database reveals some of the terminology we use to name birds is very specialized."



"It points towards an issue with how accessible these names are, such as the isabelline shrike and the diademed sandpiper-plover, even to native English speakers.”



The resource, called the <a href="https://sites.google.com/nyu.edu/avianlexiconatlas/home">AvianLexiconAtlas</a>, includes every known English-language bird species name. It categorizes the main descriptive term into one of ten thematic groups.



<h2 class="wp-block-heading" id="h-what-bird-names-reveal">What bird names reveal</h2>



The categories range from physical characteristics, like the black-capped chickadee, to natural history traits, such as the rock pigeon. They also include cultural references and geographic ties, like the European <a href="https://www.earth.com/news/starlings-are-independent-navigators-not-copycats/">starling</a>.



Some names are straightforward: the yellow-rumped warbler clearly reflects a visual trait. Others, like Wilson’s warbler or Bonaparte’s gull, reference historical figures. 



These names often reflect who discovered or classified the species more than the birds themselves. Still others - such as the barnacle goose, once thought to hatch from barnacles - have roots in outdated folklore.



<h2 class="wp-block-heading" id="h-renaming-effort-underway">Renaming effort underway </h2>



Allison Shultz is co-lead author and curator of ornithology at the Natural History Museum of Los Angeles County.



“The work gives us a rich insight into how birds are named overall,” she said. “Those naming processes can reflect all the strangeness and specificity of the people naming them, their culture, and their history - things that wouldn’t help tell you what a bird looks like.”



This disconnect between name and meaning is central to growing debates in ornithology. Names that once honored explorers or scientists are now being reconsidered. Institutions like the <a href="https://americanornithology.org/">American Ornithological Society</a> are moving to rename all species currently named after people.



The new study offers hard data to guide that shift, revealing just how few species actually fall into that category.



<h2 class="wp-block-heading" id="h-changing-how-we-name-birds">Changing how we name birds</h2>



Common names are often the public’s main entry point to a species. Just as “California <a href="https://www.earth.com/news/can-animals-feel-the-beat-ronan-the-sea-lion-might-just-prove-it/">sea lion</a>” or “brown bear” might quickly convey meaning, bird names should do the same - but many don’t.



“In ornithology, there has been significant reflection among both professional researchers and amateur naturalists about what the terminology in regionally standardized English-language common names should communicate about species of birds,” Morrison noted.



The database could help guide future renaming decisions. It offers a consistent reference for how names are formed, what they signal, and whether they help or hinder understanding.



<h2 class="wp-block-heading" id="h-classroom-idea-becomes-global-tool">Classroom idea becomes global tool</h2>



The project began in Morrison’s Life Science class at NYU in fall 2022, when students identified what type of descriptor formed the basis of a bird’s name.



They examined thousands of names and sorted them into categories: size, behavior, habitat, <a href="https://www.earth.com/news/from-dinosaurs-to-birds-the-mysterious-origin-of-feathers/">plumage</a>, geography, or human reference.



“We found that 1,000 of the 11,000 species were named after male-only plumage, but just 20 were named after female-only plumage,” Shultz said. "The orange-bellied antwren is one of the few."



Students and faculty from NYU’s Liberal Studies program contributed to the final dataset and co-authored the study.



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



The research team hopes that the AvianLexiconAtlas will serve as a foundational tool for both scientists and <a href="https://www.earth.com/news/birdwatching-can-significantly-improve-students-mental-health/">birdwatchers</a>. It includes not only the core dataset but also a glossary and a gazetteer to decode unfamiliar terms.



That may be especially helpful in parsing names like the Pincoya storm-petrel - named for a Chilean sea spirit said to dance on the waves - or the obscurely labeled baglafecht weaver.



“In the future, we look forward to combining what we learned with rich sources of data like our bird collections to understand the connections between birds and people better,” Shultz said. 



“Overall, this work provides valuable insights in helping develop approachable names that help strengthen this connection and ultimately help protect birds and nature.”



With names playing a central role in how people relate to the natural world, the project encourages a more thoughtful approach to how species are introduced, remembered, and preserved.



The study is published in the journal <a href="https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0325890">PLOS One</a>.



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Origins and oddities of bird names mapped for the first time

With names like the blue jay and the mallard, birds...

Acute diarrhea affects nearly 1 in 12 dogs annually in the UK. This stat comes from a new analysis of over 2.2 million vet health records. 



Led by Dan O’Neill at the <a href="https://www.rvc.ac.uk/" target="_blank" rel="noreferrer noopener">Royal Veterinary College</a>, this study uncovers which dogs are most at risk, what symptoms they show, and how vets treat them.



“Experiencing the dreaded ‘poonami’ with your dog is one of those events any <a href="https://www.earth.com/news/dogs-may-respond-to-each-other-through-blinking/" target="_blank" rel="noreferrer noopener">dog</a> owner fears. This new study shows that diarrhea events are very common in dogs but that owners should not panic - no matter how bad the deluge, most dogs will recover in a few days after veterinary treatment,” Dr. O’Neil noted.



<h2 class="wp-block-heading" id="h-dog-breeds-and-diarrhea-risk">Dog breeds and diarrhea risk</h2>



Some dogs are significantly more likely to suffer from diarrhea. The top at-risk <a href="https://www.earth.com/news/study-compares-dna-of-chernobyl-dogs-to-canines-living-outside-the-radiation-zone/" target="_blank" rel="noreferrer noopener">breeds</a> include Cavapoo, Maltese, Miniature Poodle, German Shepherd, Yorkshire Terrier, and Cockapoo. 



Cavapoos had the highest annual incidence risk at nearly 15 percent, followed closely by Maltese and Miniature Poodles.



Why these breeds? Genetics may play a role, but it’s also possible that lifestyle and owner behavior matter. For example, owners of popular designer crossbreeds like Cavapoos may visit vets more often, leading to more diagnoses. 



Still, even accounting for this, the odds ratios point to real predispositions, especially in Miniature Poodles and their crossbred descendants.



<h2 class="wp-block-heading" id="h-designer-breeds-face-higher-diarrhea-odds">Designer breeds face higher diarrhea odds</h2>



Designer crossbreeds like Cockapoos and Cavapoos showed a higher risk than general crossbreeds or purebreds. 



This challenges the idea that hybrid <a href="https://www.earth.com/news/dogs-can-understand-words-even-in-monotone-speech/" target="_blank" rel="noreferrer noopener">dogs</a> always benefit from hybrid vigor. Owners should be aware that these trendy dogs might need more digestive care than expected.



Interestingly, Jack Russell Terriers and Chihuahuas had lower odds of being diagnosed. These findings might help inform breed-specific guidance and early prevention efforts.



<h2 class="wp-block-heading" id="h-age-affects-dog-diarrhea-risk">Age affects dog diarrhea risk</h2>



Age stood out as a major factor. Dogs under 3 years and over 9 years had significantly higher odds of diarrhea. Puppies may eat things they shouldn’t. Older dogs might suffer due to weakened gut health or age-related illness.



The researchers found that very young dogs (under the age of one) had 2.4 times the odds of diarrhea compared to middle-aged dogs. Dogs over 14 had nearly 2.6 times the odds. For both groups, careful diet and close monitoring are key.



<h2 class="wp-block-heading" id="h-common-symptoms-and-what-to-expect">Common symptoms and what to expect</h2>



For most of the dogs in the study, diarrhea was accompanied by other symptoms. Vomiting was seen in 44 percent of cases. Reduced appetite affected 28 percent, and 24 percent were lethargic. A smaller group of dogs (about 13 percent) showed signs of abdominal pain.



Roughly 29 percent of the cases were classified as hemorrhagic (bloody). Surprisingly, blood in stools did not increase the likelihood of lab testing on the first vet visit.



<h2 class="wp-block-heading" id="h-simple-care-for-dog-diarrhea">Simple care for dog diarrhea</h2>



Most cases were managed with supportive care. Probiotics were used in 60 percent of cases. Dietary changes were prescribed in 44 percent. 



Antibiotics, though discouraged for mild cases, were still used in 38 percent of all cases. The most common was oral metronidazole.



Even more striking, 59 percent of hemorrhagic cases were treated with antibiotics, despite guidelines saying they usually should not be. These decisions seem driven by concern for the dog’s well-being and owner anxiety, not always evidence-based need.



<h2 class="wp-block-heading" id="h-is-antibiotic-overuse-a-problem">Is antibiotic overuse a problem?</h2>



Veterinary experts have warned about this for years. Antibiotics should not be the go-to for uncomplicated diarrhea. 



Overuse of antibiotics heightens the risk of resistance and gut microbiome imbalance. Yet, fear of client dissatisfaction and ingrained habits keep antibiotics in play.



A recent European panel strongly advised against giving antibiotics to dogs with mild or moderate diarrhea, even if it’s bloody. They emphasize fluid therapy and dietary support instead.



<h2 class="wp-block-heading" id="h-what-should-dog-owners-do">What should dog owners do?</h2>



Don't panic. Over 80 percent of diarrhea cases resolved with just one vet visit. Most <a href="https://www.earth.com/news/why-our-relationships-with-dogs-matter-so-much/" target="_blank" rel="noreferrer noopener">dogs</a> got better within a few days, even without lab tests or medication.



But stay alert if your dog is very young, elderly, or from a high-risk breed. Monitor for repeated episodes, especially if blood is present or other symptoms appear.



This study gives vets and owners something rare: data from real dogs, in real clinics, across the UK. The message is clear. Diarrhea is common, but most dogs recover fast. Awareness, not alarm, is the best first step.



The study is published in the journal <a href="https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0324203" target="_blank" rel="noreferrer noopener">PLOS One</a>.



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Some dogs have a higher risk of digestive problems like diarrhea

Acute diarrhea affects nearly 1 in 12 dogs annually in...

Life almost ended 252 million years ago. The end-Permian mass extinction wiped out 81% of marine life and over half of land-based <a href="https://www.earth.com/news/how-lizards-help-keep-madagascars-forests-alive/" target="_blank" rel="noreferrer noopener">species</a>. But not everything perished. Among the survivors were the archosauromorphs, small early reptiles that would later give rise to crocodiles, dinosaurs, and birds.



These <a href="https://www.earth.com/news/animals-found-to-have-a-sixth-sense-gecko-hearing-vibrations-changing-science-view-of-sound/" target="_blank" rel="noreferrer noopener">creatures</a> were not supposed to survive the intense heat of the early Triassic tropics. Scientists considered this zone nearly lifeless. 



<h2 class="wp-block-heading" id="h-ancient-reptiles-crossed-deadly-zones">Ancient reptiles crossed deadly zones</h2>



New research published in the journal Nature Ecology &amp; Evolution&nbsp;reveals that archosauromorphs did more than endure the deadly zone. They moved through it.



Using a modeling system called TARDIS, which maps dispersal across time and space, researchers estimated the migration routes of 392 archosauromorph species. 



The model linked fossils with landscape data and climate reconstructions, exposing hidden paths through so-called inhospitable regions.



<h2 class="wp-block-heading" id="h-climate-adaptability-and-niche-expansion">Climate adaptability and niche expansion</h2>



The study showed that these reptiles had much wider climate tolerances than fossil <a href="https://www.earth.com/news/reptile-ancestors-appeared-40-million-years-earlier-than-we-thought/" target="_blank" rel="noreferrer noopener">evidence</a> alone suggested. They adapted to extreme environments, including hot and dry zones with high temperature seasonality and low rainfall.



This ability to cross geographic and climatic barriers helped them enter new ecological niches. These movements likely shaped the evolutionary path that led to the rise of dinosaurs.



<h2 class="wp-block-heading" id="h-how-ancient-reptiles-outlived-extinction">How ancient reptiles outlived extinction</h2>



“Amid the worst climatic event in Earth’s history, where more <a href="https://www.earth.com/news/fossil-discovery-pushes-back-reptile-evolution-by-40-million-years/" target="_blank" rel="noreferrer noopener">species</a> died than at any period since, life still survived," said Dr. Joseph Flannery-Sutherland from the <a href="https://www.birmingham.ac.uk" target="_blank" rel="noreferrer noopener">University of Birmingham</a>, who led the study.



"We know that archosauromorphs as a group managed to come out of this event and over the Triassic period became one of the main players in shaping life thereafter."



“Gaps in their fossil record have increasingly begun to tell us something about what we weren’t seeing when it comes to these reptiles. Using our modeling system, we have been able to build a picture of what was happening to the archosauromorphs in these gaps and how they dispersed across the ancient world."



According to Dr. Flannery-Sutherland, the results of the study suggest that these reptiles were much hardier to the extreme climate of the Pangaean tropical dead zone, able to endure these hellish conditions to reach the other side of the world. 



"It’s likely that this ability to survive the inhospitable tropics may have conferred an advantage that saw them thrive in the Triassic world," he noted. 



<h2 class="wp-block-heading" id="h-tracking-evolutionary-radiation">Tracking evolutionary radiation</h2>



The paper describes how the reptiles’ dispersal began in the northern supercontinent Laurasia. Over time, they crossed Central Pangaean mountains and entered southern Gondwana. 



By the Wordian stage, long-distance movements had begun. These ancient reptiles not only traveled across land but also ventured into regions that lacked any fossil record. These regions were once thought off-limits.



The team found that climate conditions during these travels included both very high temperatures and arid environments. Their movement wasn’t random. It often followed low-elevation coastal routes, sometimes aided by monsoon-like humidity along ancient seashores.



“The evolution of life has been controlled at times by the environment, but it is difficult to integrate our limited and uncertain knowledge about the ancient landscape with our limited and uncertain knowledge about the ecology of extinct organisms," noted Professor Michael Benton, senior author of the study.



"But by combining the fossils with reconstructed maps of the ancient world, in the context of evolutionary trees, we provide a way of overcoming these challenges.” 



<h2 class="wp-block-heading" id="h-capturing-the-full-story-of-reptiles">Capturing the full story of reptiles</h2>



The oldest fossils were found in Europe, but that may reflect better sampling rather than true origins. The study's models show that archosauromorphs could have existed elsewhere long before they appeared in the fossil record. 



In fact, dispersal paths into South America and North America predate the oldest known fossils there by up to 15 million years.



By measuring climate variables along these ancient migration routes, the researchers captured broader ecological diversity than fossils alone could show. This reveals how species adapted as they moved through different environments.



<h2 class="wp-block-heading" id="h-tracking-other-ancient-animals">Tracking other ancient animals</h2>



The authors suggest that similar modeling approaches could apply to other ancient lineages with poor fossil records. By coupling evolutionary trees with climate and terrain data, scientists can rebuild missing chapters of evolutionary history.



These early reptiles didn’t just bounce back from catastrophe. They reshaped their world through resilience and movement. Their journey laid the groundwork for the age of dinosaurs and ultimately modern birds and crocodiles.



The study is published in the journal <a href="https://www.nature.com/articles/s41559-025-02739-y" target="_blank" rel="noreferrer noopener">Nature Ecology &amp; Evolution</a>.



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Reptiles survived 'hellish' conditions during Earth's worst climate crisis

Life almost ended 252 million years ago. The end-Permian mass...

Forests, mountains, and deserts are home to a quiet and elusive animal: the cougar. Often overlooked and frequently misunderstood, this powerful predator plays a vital role in North America’s ecosystems. 



On National Cougar Day, June 12, 2025, we take a closer look at the importance of this remarkable species - and the challenges it faces.



National Cougar Day isn’t just about appreciation - it’s a reminder that coexistence matters. It calls on us to learn, adapt, and do our part to protect the wild places and species that still survive alongside us.



As habitat loss and biodiversity decline continue, cougars have become a symbol of resilience. Their ability to survive in changing landscapes highlights the delicate balance of <a href="https://www.earth.com/news/cougars-hunt-smaller-prey-to-avoid-conflict-with-other-predators/" target="_blank" rel="noreferrer noopener">ecosystems</a> - and the critical role top predators play in keeping that balance intact.



<h2 class="wp-block-heading" id="h-the-cougar-s-place-in-nature">The cougar’s place in nature</h2>



Cougars, also known as mountain lions or pumas, are the most widely distributed wild cats in the Western Hemisphere. From the Canadian Yukon to the Andes Mountains of South America, these animals traverse grasslands, deserts, forests, and mountains. 



Despite their wide range, they remain elusive, mostly avoiding humans while maintaining an essential role in local <a href="https://www.earth.com/news/national-cougar-day-the-crucial-ecological-role-of-cougars/" target="_blank" rel="noreferrer noopener">ecosystems</a>.



As apex predators, cougars help control prey populations, especially deer. This influences vegetation growth and benefits many other species. A balanced food chain reduces overgrazing, supports plant diversity, and stabilizes the broader environment. 



Cougars act as nature’s regulators, making sure that no species overwhelms the rest. Their role is subtle but foundational.



<h2 class="wp-block-heading" id="h-why-national-cougar-day-was-created">Why National Cougar Day was created</h2>



National Cougar Day was established in 2019 to celebrate the ecological importance of cougars and draw attention to the threats they face.



Despite their broad range, cougars face habitat loss, human encroachment, road mortality, and lethal management policies in several states. These pressures grow stronger each year.



National Cougar Day seeks to change perceptions. It replaces fear with understanding, myth with science, and confrontation with coexistence. 



Conservation groups use the occasion to spread awareness, share research, and advocate for laws that protect cougars and the <a href="https://www.earth.com/news/apex-predators-can-help-restore-ecosystems-but-not-immediately/" target="_blank" rel="noreferrer noopener">ecosystems</a> they support.



<h2 class="wp-block-heading" id="h-a-clear-focus-in-2025">A clear focus in 2025</h2>



National Cougar Day 2025 echoes a clear message across conservation <a href="https://mountainlion.org" target="_blank" rel="noreferrer noopener">communities</a>: coexistence. 



This year, many wildlife groups are focusing on practical ways to help humans and cougars share space safely. Instead of pushing them out or hunting them down, experts are encouraging informed policies and education.



This focus matters. Urban expansion enters cougar territory more each year, increasing the chance of conflict. Without education, these encounters often lead to tragic outcomes. Most often, it is the cougar that pays the price. 



Understanding how to prevent conflict can change this trend. Learning to interpret cougar behavior and create safe environments helps both humans and animals.



Coexistence includes wildlife corridors, community education, and responsible livestock management. These strategies already show positive results in some regions. They could provide the foundation for broader, lasting harmony between people and wildlife.



<h2 class="wp-block-heading" id="h-growing-threats-to-cougars">Growing threats to cougars</h2>



Cougars are not globally endangered, but their numbers decline in certain regions. Expanding human development slices through their migration paths. Roads, fences, and housing projects isolate populations. This leads to genetic bottlenecks and weakens long-term survival.



Some U.S. states continue to allow cougar hunting under wildlife management plans. While intended to regulate populations, studies show that this often creates instability. When dominant adult cougars are killed, young males take over, leading to more unpredictable behavior and increased human conflict.



The cougar’s greatest threat is human misunderstanding. For decades, stories and media shaped a fearful image. National Cougar Day invites us to look again. Science-based policies can ensure a future where cougars and people thrive together.



<h2 class="wp-block-heading" id="h-moving-forward-with-intention">Moving forward with intention</h2>



National Cougar Day 2025 comes during a time of growing environmental awareness. Climate change, habitat loss, and biodiversity decline dominate global conversations. 



In that context, the cougar’s story offers something different. It offers hope. Unlike many species in crisis, cougars still roam across vast areas. We still have time to act wisely.



This day invites thoughtful action. Watching a documentary, reading wildlife science, or supporting a <a href="https://cougarconservancy.org/save-la-cougars" target="_blank" rel="noreferrer noopener">conservation campaign</a> can all help. Better awareness leads to smarter policies. Informed communities become protectors, not opponents.



By standing up for cougars, we stand up for healthy landscapes. Their survival means the ecosystem is still working. Their absence would show a system in collapse. 



When we protect cougars, we also protect every creature that depends on the balance they maintain.



<h2 class="wp-block-heading" id="h-significance-of-national-cougar-day">Significance of National Cougar Day </h2>



National Cougar Day is an opportunity to recognize an animal that often goes unnoticed but plays a vital role in the natural world. 



Cougars don’t demand attention - they survive quietly, shaping ecosystems simply by being part of them. But today, they face growing threats, and their future depends on our awareness and action. 



June 12 is a chance to learn, to speak up, and to support efforts that keep wild places wild - with cougars still a part of them.



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National Cougar Day 2025: Peacefully coexisting with wildlife

Forests, mountains, and deserts are home to a quiet and...

Pigs stand out among domestic animals for their intelligence, social behavior, and ability to adapt to various environments. But their historical journey from wild creatures to companions in early agricultural societies is just as compelling.



Across centuries, they have played vital roles in food systems, cultural traditions, and even scientific research. Their domestication marks not only a biological transformation but also a deepening relationship between humans and <a href="https://www.earth.com/news/from-wolves-to-dogs-did-domestication-begin-without-human-help/" target="_blank" rel="noreferrer noopener">animals</a>.



A new study, led by researchers from <a href="https://home.dartmouth.edu" target="_blank" rel="noreferrer noopener">Dartmouth</a>, offers fresh insight into that transformation. The findings trace the origins of pig domestication back nearly 8,000 years, placing the earliest known human-pig interactions in South China. 



This discovery does more than date an evolutionary milestone. It adds depth to our understanding of how early agricultural communities shaped - and were shaped by - the animals around them.



<h2 class="wp-block-heading" id="h-tracing-the-first-domesticated-pigs">Tracing the first domesticated pigs</h2>



For years, scholars believed China might be one of the centers where pigs were first <a href="https://www.earth.com/news/all-domestic-horses-have-ancestors-in-russia/" target="_blank" rel="noreferrer noopener">domesticated</a>. However, evidence remained scattered and incomplete. This new research bridges that gap. 



The study shows that pigs living near humans began to eat leftover cooked food and scavenge waste during the early Neolithic period, around 8,000 years ago. 



This was the time in which humans shifted from foraging to farming and made their earliest attempts at domestication. Among the species they tried to domesticate were wild boars - large, fierce creatures with big heads and strong teeth.



"While most wild boars are naturally aggressive, some are more friendly and less afraid of people, which are the ones that may live alongside humans," explained lead author Jiajing Wang. 



"Living with humans gave them easy access to food, so they no longer needed to maintain their robust physiques."



As a consequence, their characteristics underwent changes. "Over time, their bodies became smaller, and their brains also became smaller by about one-third," Wang said.



<h2 class="wp-block-heading" id="h-pig-teeth-reveal-early-signs-of-domestication">Pig teeth reveal early signs of domestication</h2>



Traditionally, archaeologists examine bones to detect <a href="https://www.earth.com/news/sheep-have-been-intertwined-with-humans-for-over-11000-years/" target="_blank" rel="noreferrer noopener">domestication</a>. But this method can miss early behavioral changes. "What probably came first were behavioral changes, like becoming less aggressive and more tolerant of humans," noted Wang.



So the team used a different approach. They analyzed dental calculus - plaque buildup - on 32 pig teeth. These came from ancient sites in the Lower Yangtze River region: Jingtoushan and Kuahuqiao.



Waterlogged conditions helped preserve the organic material. Researchers recovered 240 starch granules from the plaque deposits. These showed that the pigs had eaten cooked rice, yams, an unknown tuber, acorns, and grasses.



"These are plants that were present in the environment at that time and were found in human settlements," said Wang.



<h2 class="wp-block-heading" id="h-pigs-lived-closely-with-humans">Pigs lived closely with humans</h2>



The researchers found another sign of pig-human intimacy: parasite eggs. Specifically, whipworm eggs. These eggs can grow inside human intestines. They showed up in 16 pig specimens and represent the earliest archaeological evidence of human whipworm in East Asia.



"Pigs are known for their habit of eating human waste, so that is additional evidence that these pigs were probably living with humans or having a very close relationship with them," noted Wang.



Wang also added that pigs do not cook food for themselves, so were probably being fed scraps from human food, or possibly scavenging the scraps from waste sites. 



<h2 class="wp-block-heading" id="h-pig-domestication-and-scavenging">Pig domestication and scavenging</h2>



The team also studied tooth sizes. Some pigs had teeth like today’s <a href="https://www.earth.com/news/chicken-domestication-humans-timeline-silk-road-evidence/" target="_blank" rel="noreferrer noopener">domestic</a> pigs. This supports the idea that some were already under human care .



"Wild boars were probably attracted to human settlements as people started settling down and began growing their own food," said Wang. 



"These settlements created a large amount of waste, and that waste attracts scavengers for food, which in turn fosters selection mechanisms that favored animals willing to live alongside humans."



This supports the “commensal pathway” theory - animals first came for food, not because humans wanted to tame them. But Wang’s team also saw signs of the “prey pathway,” where people began managing pigs directly.



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



"Our study shows that some wild boars took the first step towards domestication by scavenging human waste," concluded Wang.



This study also highlights a key issue: living close to animals can spread diseases. Parasite transfer likely began early in human settlements.



The research involved several scholars: Yiyi Tang, Yunfei Zheng, Leping Jiang, Guoping Sun, Xiaolin Ma, and Yanfeng Hou. Their work brings us closer to understanding the long, messy, and fascinating journey of pig domestication.



The study is published in the journal <a href="https://www.pnas.org/doi/10.1073/pnas.2507123122" target="_blank" rel="noreferrer noopener">Proceedings of the National Academy of Sciences</a>.



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Biologists finally unravel the surprising story of how humans domesticated pigs

Pigs stand out among domestic animals for their intelligence, social...

Each year on June 11, the world turns its attention to a quiet predator. International Lynx Day celebrates the mysterious and solitary lynx, one of the forest’s most skilled hunters. 



In 2025, the event serves as both a tribute and a call to action. The lynx may seem invisible in the wild, but their presence shapes entire ecosystems.



This day reminds us of the delicate balance between nature and human development. It invites reflection, education, and renewed commitment to preserving the <a href="https://www.earth.com/news/protecting-lynx-habitat-in-a-shifting-landscape/" target="_blank" rel="noreferrer noopener">species</a>. As pressures on forests intensify, the lynx remains a symbol of resilience, solitude, and environmental health. 



<h2 class="wp-block-heading" id="h-a-closer-look-at-the-lynx-family">A closer look at the lynx family</h2>



The lynx belongs to a small but mighty group within the cat family. There are four distinct species: the Eurasian lynx, the Canada lynx, the Iberian lynx, and the bobcat. 



All share tufted ears, large paws, and a taste for stealth. These <a href="https://www.earth.com/news/saving-the-iberian-lynx-how-humans-rescued-this-rare-feline-from-extinction/" target="_blank" rel="noreferrer noopener">animals</a> live across varied landscapes, from snowy boreal forests to rugged Mediterranean terrain.



The Eurasian lynx is the largest, thriving in pockets across Europe and Asia. The Canada lynx, adapted for deep snow, follows the snowshoe hare's cycle. 



The Iberian lynx, once the most endangered feline in the world, roams the Iberian Peninsula. The bobcat, North America’s smallest lynx species, is widespread but often misunderstood.



Each lynx plays a vital ecological role. They keep prey populations in check, maintain healthy forests, and support biodiversity. However, despite their adaptability, these animals face rising threats that challenge their survival across the globe.



<h2 class="wp-block-heading" id="h-dramatic-recovery-of-the-iberian-lynx">Dramatic recovery of the Iberian lynx</h2>



Of all the lynx <a href="https://www.earth.com/news/canada-lynxs-historic-range-points-to-a-promising-future/" target="_blank" rel="noreferrer noopener">species</a>, the Iberian lynx’s comeback is the most dramatic. In the early 2000s, fewer than 100 individuals remained in the wild. Conservationists feared extinction. Then came a surge of action: breeding programs, habitat protection, and public awareness campaigns.



Today, there are over 2,000 Iberian lynx roaming free. The species has moved from "Critically Endangered" to "Endangered" on the <a href="https://www.iucnredlist.org" target="_blank" rel="noreferrer noopener">IUCN Red List</a>. “This is one of the greatest conservation success stories of the 21st century,” said Miguel Ángel Simón, a leading lynx conservationist in Spain.



Despite this progress, dangers persist. Lynx often fall victim to vehicle collisions. Encroaching development fragments their habitat. 



Conservation groups warn that if momentum slows, the population could stall or reverse. Continued protection, monitoring, and expansion of territory remain critical for the Iberian lynx to thrive long term.



<h2 class="wp-block-heading" id="h-habitat-fragmentation-a-shared-threat">Habitat fragmentation: A shared threat</h2>



All lynx <a href="https://www.earth.com/news/canada-lynx-survival-linked-to-life-cycle-of-snowshoe-hares/" target="_blank" rel="noreferrer noopener">species</a> depend on large, connected forests. When these habitats become isolated, their survival grows uncertain. Roads, farms, and fences block their natural movement. This not only leads to accidents but also weakens genetic diversity through inbreeding.



In Europe, rewilding efforts have reintroduced lynx to places like the Alps, Jura Mountains, and parts of the Balkans. These animals show strong adaptability when given the space. Yet gaps remain. Connectivity between territories is often poor.



In North America, especially Canada, logging and climate change impact the snowshoe hare. With their main prey in decline, lynx populations also suffer. Meanwhile, bobcats, though more resilient, struggle with suburban expansion and reduced prey.



Conservationists argue that saving lynx means more than protecting forest patches. It requires landscape-scale planning and collaboration across borders and communities.



<h2 class="wp-block-heading" id="h-honoring-international-lynx-day">Honoring International Lynx Day </h2>



This year’s International Lynx Day pushes for deeper thinking about conservation. It emphasizes both physical and emotional ties. Forests must be reconnected through wildlife corridors. But people also need to reconnect with nature and with each other.



Wildlife crossings such as green bridges and tunnels are gaining popularity. These help lynx cross busy roads without risk. Forest buffers between farms and wild zones also create safe paths. Some regions in Germany and Switzerland have already seen benefits from such solutions.



Public engagement forms the heart of these efforts. Many communities hold nature walks, host talks, and run school programs during International Lynx Day. Young people, in particular, are seen as crucial allies.



<h2 class="wp-block-heading" id="h-public-perception-and-coexistence">Public perception and coexistence </h2>



Living alongside lynx is not always easy. In some regions, livestock predation fuels resentment. Hunters sometimes see lynx as competition. But research shows that these conflicts often come from misunderstanding.



Lynx are shy and rarely seen. They prefer deer or hares to sheep or goats. Many attacks on livestock are wrongly blamed on them. 



Education and compensation schemes have helped reduce these tensions. In Portugal and Spain, coexistence training has made local farmers more willing to support lynx programs.



Art, film, and storytelling also help reshape public perception. The cultural approaches, when combined with scientific ones, create lasting change.



<h2 class="wp-block-heading" id="h-take-action-on-international-lynx-day">Take action on International Lynx Day </h2>



The lynx does not demand loud attention. It walks quietly, blends in, and keeps to itself. But its survival depends on our willingness to act. International Lynx Day challenges individuals and governments alike.



You do not need to see a lynx in the wild to help. By protecting forests, supporting conservation groups, and spreading awareness, you contribute to their survival. Every tree preserved, every corridor built, and every child educated brings the lynx closer to safety



Let this year’s celebration be more than symbolic. Let it be a turning point where connection becomes action and the silent footsteps of the lynx continue to echo through the forests for generations to come.



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International Lynx Day 2025: Protecting the silent hunters of the forest

Each year on June 11, the world turns its attention...

Each year, more than two trillion wild and farmed fish are killed to feed humanity. Their deaths often go unnoticed. Yet beneath the surface is a simple biological fact: fish can suffer.



Rainbow trout, a <a href="https://www.earth.com/news/small-fish-provide-climate-resilient-nutrition-for-a-warming-world/" target="_blank" rel="noreferrer noopener">species</a> farmed and consumed across the globe, experience not just death - but a prolonged and intense form of distress when killed by air asphyxiation. 



A new study published in the journal Scientific Reports shines a light on this pain and offers a pathway to reduce it.



<h2 class="wp-block-heading" id="h-fish-pain-needs-better-measurement">Fish pain needs better measurement</h2>



Unlike environmental impact or public health, <a href="https://www.earth.com/news/crabs-lobsters-crustaceans-feel-pain-calls-for-immediate-ban-on-boiling-them-alive/" target="_blank" rel="noreferrer noopener">animal suffering lacks a universal metric</a>. There are no equivalents to carbon footprints or life years lost. To address this, scientists developed the Welfare Footprint Framework (WFF).



This tool measures pain in minutes, allowing researchers to compare welfare outcomes across species and <a href="https://www.earth.com/news/world-oceans-day-2025-sustaining-what-sustains-us/" target="_blank" rel="noreferrer noopener">conditions</a>. The research team applied this method to trout slaughter, where air exposure is still a widely used technique.



Fish, when pulled from water, begin a slow and stressful decline. Their gills collapse. They gasp in panic. Their blood chemistry spirals. Oxygen disappears while carbon dioxide builds. 



These biological reactions unfold as the fish continues to move, gasp, and suffer - sometimes for as long as 25 minutes.



<h2 class="wp-block-heading" id="h-fish-suffer-up-to-25-minutes">Fish suffer up to 25 minutes </h2>



The researchers divided the trout's suffering into four time segments. These range from alarm at removal to the final depression of brain activity before unconsciousness. 



Through behavioral, neurological, and pharmacological evidence, the team estimated that the average trout endures about ten minutes of pain that qualifies as hurtful, disabling, or excruciating. 



In some conditions, this could stretch beyond 20 minutes. When adjusted by weight, that translates to 24 minutes of such pain per kilogram (about 11 minutes per pound) of fish killed.



The team used neurophysiological data like EEG signals and reflex loss to identify unconsciousness. They reviewed how fish respond to CO₂, pH imbalance, muscle exhaustion, and fear-inducing stimuli. Each pain level had specific criteria, ranging from annoyance to total disruption of basic functions.



<h2 class="wp-block-heading" id="h-current-methods-cause-painful-deaths">Current methods cause painful deaths</h2>



Air asphyxiation is still legal and common in many parts of the world. But it is neither quick nor painless. Chilling in ice or using ice slurry might sound gentler, yet for cold-adapted species like trout, this method just slows down metabolism. 



This can delay loss of consciousness even further, compounding the suffering. Ice exposure also risks tissue damage, thermal shock, and prolonged fear.



The research shows that suffering does not always begin at the point of slaughter. It often starts well before. 



Crowding, transport, and handling all add to the <a href="https://www.earth.com/news/fish-thought-extinct-for-85-years-reappears-in-himalayan-river-chel-snakehead/" target="_blank" rel="noreferrer noopener">fish</a>’s cumulative pain. These pre-slaughter stressors can cause physical injury and hours of distress. Yet, regulations usually overlook them.



<h2 class="wp-block-heading" id="h-stunning-can-help-fish-suffer-less">Stunning can help fish suffer less </h2>



The study evaluated two types of stunning: electrical and percussive. Electrical stunning, if properly used, could spare 60 to 1,200 minutes of suffering for every dollar spent. This makes it one of the most cost-effective welfare interventions known. 



But implementation remains inconsistent. In many commercial settings, electrical stunning fails to reliably render fish unconscious. Poor placement of electrodes, inadequate voltage, or faulty machines may undermine the potential benefits.



Percussive stunning - a physical blow to the head - has shown better consistency in lab settings. But it's difficult to scale. Fish vary in size. Equipment must be precisely calibrated. Worker fatigue also reduces effectiveness. Any slip means the fish remains conscious while bleeding out.



<h2 class="wp-block-heading" id="h-a-new-language-for-animal-pain">A new language for animal pain</h2>



What makes the Welfare Footprint Framework powerful is its transparency. Instead of assigning a fixed label to pain, it works with probabilities. If scientists believe there's a 40% chance the pain is disabling and a 40% chance it is excruciating, the framework includes both.



This makes the model flexible and more reflective of real-world uncertainty. Pain, like emotion, varies between individuals. Some fish may suffer more than others, even under identical conditions.



"The Welfare Footprint Framework provides a rigorous and transparent evidence-based approach to measuring <a href="https://www.earth.com/news/small-fish-species-are-the-big-catch-of-the-future/" target="_blank" rel="noreferrer noopener">animal</a> welfare, and enables informed decisions about where to allocate resources for the greatest impact," noted Dr. Wladimir Alonso from <a href="https://welfarefootprint.org" target="_blank" rel="noreferrer noopener">Welfare Footprint Institute</a>.



This approach mirrors models used in public health or environmental science. Just like life years lost to disease, we can now talk about minutes of suffering saved.



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



Fish slaughter occupies only minutes in an animal’s life - but these minutes can be extremely painful. Compared to long-term reforms on farms, slaughter improvements are easier to implement and affect billions of lives. 



The study's authors argue that investing in better stunning tools and training workers can provide enormous welfare gains.



For policy makers, this research offers a scientific foundation to reform outdated practices. Certification schemes can set minimum stunning effectiveness based on real pain data. 



Governments can use this to guide humane slaughter laws. For consumers, it gives a new way to think about what ends up on their plate.



<h2 class="wp-block-heading" id="h-other-fish-suffer-too">Other fish suffer too</h2>



Though this study focused on rainbow trout, the underlying stress pathways - oxygen deprivation, acidosis, metabolic failure - are common across fish species. That means the Welfare Footprint Framework can be adapted. 



Salmon, catfish, seabass, tilapia - they all may suffer in similar ways during air exposure. However, each species will need specific data. 



Some tolerate low oxygen better. Others may react more strongly to ice. Future research must expand to include this diversity.



<h2 class="wp-block-heading" id="h-a-turning-point-for-aquatic-welfare">A turning point for aquatic welfare</h2>



The world is just beginning to reckon with the sentience of fish. For decades, their pain was denied or ignored. But science no longer allows that. 



With trillions of fish slaughtered every year, even small improvements can have vast impact.



The WFF doesn’t just measure pain. It opens a language of empathy grounded in evidence. It lets regulators, producers, and consumers weigh the cost of change. 



And perhaps, most importantly, the framework acknowledges what fish have felt all along - suffering that deserves to be seen and reduced.



The study is published in the journal <a href="https://www.nature.com/articles/s41598-025-04272-1" target="_blank" rel="noreferrer noopener">Scientific Reports</a>.



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Scientists prove fish suffer "intense pain" for at least 10 minutes after catch, calls made for reforms

Each year, more than two trillion wild and farmed fish...

A turtle’s head seems simple: a hard beak, two bright eyes, and a quilt of scales that protect the skull. Look closer and a mystery appears, because the polygons across the crown don’t line up with the neat rows along the cheeks.



A team at the <a href="https://www.unige.ch/en/" target="_blank" rel="noreferrer noopener">University of Geneva</a> reports that the crown and the cheeks form in totally different ways. The study combines <a href="https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/dna-profiling" target="_blank" rel="noreferrer noopener">genetic profiling</a>, 3D microscopy, and computer models to show that turtles first lay down chemical cues, then let physics crease the remaining skin.



According to researchers, the split strategy provides a window into <a href="https://www.earth.com/news/world-turtle-day-2025-ancient-creatures-with-modern-challenges/" target="_blank" rel="noreferrer noopener">turtle</a> ancestry and perhaps even the faces of dinosaurs.



<h2 class="wp-block-heading" id="h-turtle-cheeks-follow-a-genetic-pattern">Turtle cheeks follow a genetic pattern</h2>



In most vertebrates, appendages such as feathers, hair, and ordinary body scales begin in tiny thickened patches called <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC3607644/" target="_blank" rel="noreferrer noopener">placodes</a>. These patches appear when a <a href="https://www.nature.com/articles/s41598-020-60853-2" target="_blank" rel="noreferrer noopener">reaction-diffusion system</a> nudges neighboring cells to switch certain genes on and off, spacing the primordia like points on graph paper.



Because each placode runs its own mini-program, the final pattern is orderly, and the resulting scales, follicles, or feathers sit in tidy ranks. That tidy plan applies to the edges of a turtle’s head, too. 



The Geneva team found clear <a href="https://www.earth.com/news/sea-turtles-use-earths-magnetic-field-like-an-invisible-map/" target="_blank" rel="noreferrer noopener">gene</a> activity: <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC3578394/" target="_blank" rel="noreferrer noopener">β-catenin and sonic hedgehog</a> in those peripheral zones match the classic placode signature.



Once a placode finishes its job, chemistry rests, keratin hardens, and the skin in that area stops changing shape.



<h2 class="wp-block-heading" id="h-turtle-crown-scales-form-by-folding">Turtle crown scales form by folding</h2>



Crocodiles break the <a href="https://pubmed.ncbi.nlm.nih.gov/39663449/" target="_blank" rel="noreferrer noopener">placode rule</a>. Their head scales arise when faster-growing surface skin buckles against slower bone, a purely mechanical fold that needs no gene switch. 



The same kind of buckling sculpts the folds of the <a href="https://www.pnas.org/doi/10.1073/pnas.1406015111" target="_blank" rel="noreferrer noopener">mammalian brain</a>, where expanding gray matter crumples against the white-matter core.



“Patterns that rely on physics can vary from side to side in the same <a href="https://www.earth.com/news/young-sea-turtles-swim-and-choose-their-paths-instead-of-drifting/" target="_blank" rel="noreferrer noopener">animal</a>,” explained Rory Cooper, a postdoctoral researcher at Geneva and lead author of the study. 



Mechanical folding follows rules of thickness, stiffness, and relative growth, so tiny shifts in any layer produce new polygons, rivulets, or wrinkles.&nbsp;That variability makes a crocodile’s faceprint unique enough for field biologists to use like a fingerprint.



<h2 class="wp-block-heading" id="h-turtles-use-two-methods-for-head-scales">Turtles use two methods for head scales</h2>



Turtles, it turns out, run chemistry along the cheeks and jaws, then hand the baton to mechanics on the crown. Gene markers vanish from the top of the head just as the skull bone stiffens underneath, and the skin above starts to thicken.



“This mechanical folding explains the asymmetrical shapes of the scales on the top of the head,” said Cooper. 



Study co-author Ebrahim Jahanbakhsh noted that even the left and right sides of a single turtle rarely match, a hallmark of spontaneous folding.



Finite-element simulations that tweak skin stiffness, growth speed, and bone anchoring replay the exact ridges seen in sulcata, Greek, and marginated tortoises.



<h2 class="wp-block-heading" id="h-where-scale-patterns-fail">Where scale patterns fail</h2>



Most reptiles rely on consistent scale formations for protection and <a href="https://www.earth.com/news/beating-the-heat-how-sea-turtles-cope-with-warming-waters/" target="_blank" rel="noreferrer noopener">species</a> identification. But when patterning becomes unpredictable, as it does on the top of a tortoise’s head, it raises questions about function versus aesthetics.



In these regions, the irregular folds likely don’t impact survival but instead represent a byproduct of how the skin and skull grow. 



These unpredictable folds might offer minor benefits like increased flexibility or abrasion resistance, but researchers say there's no evidence they serve a specialized purpose.



<h2 class="wp-block-heading" id="h-comparing-species-and-scale-styles">Comparing species and scale styles</h2>



Not all tortoises use mechanical folding to the same extent. The sulcata tortoise shows deeply creased central scales, while the marginated tortoise has smoother, simpler head patterns.



These variations suggest that species-specific differences in skin stiffness, skull growth rate, or layer thickness shape the final outcome. 



This diversity means researchers can use head scale patterns not only to explore mechanics but also to better understand how evolution tweaks physical properties without rewriting genetic code.



<h2 class="wp-block-heading" id="h-turtle-head-scales-linked-to-dinosaurs">Turtle head scales linked to dinosaurs</h2>



Crocodiles and turtles sit on neighboring branches of the reptile tree, with birds perched a step away. Finding the same mechanical folding in both turtles and crocodiles implies that their common ancestor, likely a <a href="https://www.nps.gov/pefo/learn/triassic-reptiles.htm" target="_blank" rel="noreferrer noopener">Triassic reptile</a>, already used this trick.



“Mechanical patterning is an ancient trait that birds later lost,” noted study co-author Michel Milinkovitch. 



If so, dinosaurs may have carried random polygonal head scales that formed without placodes - a detail never preserved in fossils but now hinted at in living cousins.



That insight reshapes how paleontologists imagine soft-tissue textures on extinct archosaurs.



<h2 class="wp-block-heading" id="h-broader-implications-of-the-research">Broader implications of the research</h2>



The study also feeds the growing field of <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC10204470/" target="_blank" rel="noreferrer noopener">biomimetics</a>. Nature often solves mechanical problems with minimal materials, and engineers copy those solutions into flexible electronics, shock-absorbing panels, and adaptive building skins.



A scale network that emerges from simple growth stresses, without a genetic template, offers a blueprint for surfaces that morph on their own when conditions change. 



Architects already explore folding façades that open like pinecones or wrinkle like leaves; turtle crowns add a new motif where randomness is a feature, not a flaw.



Regenerative-medicine researchers see a parallel in wound healing, where guiding skin to buckle or relax could help close irregular gaps. Even 3D-printing specialists may adapt the Geneva algorithms to program self-folding films for soft robots.



The study is published in the journal <a href="https://linkinghub.elsevier.com/retrieve/pii/S2589004225009459" target="_blank" rel="noreferrer noopener">iScience</a>.



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Turtle heads reveal an ancient reptilian secret

A turtle’s head seems simple: a hard beak, two bright...

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