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

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

A ten-year, nearly 2,000-station ocean survey has uncovered a diffuse veil of plastics drifting through every sampled layer of the North Atlantic ocean and adjoining basins. The findings suggest that plastic pollution penetrates far deeper than earlier studies implied.



The work, led by a team of <a href="https://www.northeastern.edu/">Northeastern University</a> marine scientists, characterizes a suspended “light smog” of synthetic fragments and fibers - many thinner than a human hair. These particles ride currents, mix vertically, and settle slowly toward the deep sea.



<h2 class="wp-block-heading" id="h-a-3d-ocean-plastic-problems">A 3D ocean plastic problems</h2>



For years, marine plastic researchers investigated the surface garbage patches concentrated by slow-moving gyres. Those rotating currents still host prodigious amounts of floating waste, but the new analysis shows that gyre dynamics do not stop at the surface.



“You’ve got these accumulations on the surface, and the same processes concentrating and leading to accumulations below the gyres into a sort of lens,” said senior author Aron Stubbins, a marine scientist at Northeastern.



The team combined plankton-net tows, in-line filtration, pump casts, and sediment traps collected between 2014 and 2024.



Most sites lay in the Northern Hemisphere’s busy shipping lanes and coastal margins - regions with dense coastal populations and well-documented mismanaged waste.



Even so, researchers were surprised by the reach of <a href="https://www.earth.com/news/plastic-pollution-is-changing-the-entire-earth-system/">plastic pollution</a>. “Plastics are more or less everywhere,” Stubbins said. “We’re finding them deposited in the Antarctic, in the Himalayas, carried by the wind, but to find them well-distributed throughout the ocean is surprising.”



<h2 class="wp-block-heading" id="h-heavy-plastics-don-t-always-sink">Heavy plastics don’t always sink</h2>



Buoyant polymers such as polyethylene and polypropylene naturally ride the waves. Denser resins, including polyethylene terephthalate (PET) from water bottles, should in theory fall quickly to the seabed. Yet PET showed up at multiple mid-water depths.



“One rationale is that when something is small enough, its density becomes less important than its drag,” Stubbins noted. 



In other words, once abrasion, UV exposure, and microbial attack whittle a bottle fragment into a sub-100-micron shard, turbulent eddies can keep it aloft for months or years.



The survey found <a href="https://www.earth.com/news/microplastics-spread-deep-into-the-ocean-far-below-the-surface/">microplastics</a> in all studied size classes, but concentrations peaked below 20 microns. Particles in this range behave almost like mineral dust in air: they scatter sunlight, adsorb chemicals efficiently, and are easily inhaled - by <a href="https://www.earth.com/news/plankton-at-risk-global-warming-threatens-the-oceans-lifeline/">plankton</a> in this case, rather than people.



<h2 class="wp-block-heading" id="h-ripples-through-the-food-web">Ripples through the food web</h2>



Tiny plankton form the base of <a href="https://www.earth.com/news/oceans-twilight-zone-stabilizes-the-marine-food-chain/">marine food chains</a>, fueling everything from larval fish to baleen whales.



Laboratory studies show that copepods and krill readily ingest micro- and nanoplastics, mistaking them for nutritious algae. Field data remain sparse, but the scientists warn that real-world exposure may be higher than previously estimated.



“In terms of the food chain, there could be interaction,” Stubbins said. “Organisms could be feeding in these zones and ingesting these plastics and also the toxic passenger molecules they carry, which could distribute into fish tissue, and we end up consuming them.”



Plastic particles act as rafts for organic pollutants, trace metals, and pathogenic microbes, meaning that a single 10-micron bead can deliver a chemical cocktail to any predator that swallows it. 



The long-distance drift documented in the new study therefore multiplies the potential contact between pollutants and wildlife.



<h2 class="wp-block-heading" id="h-plastics-may-trap-carbon">Plastics may trap carbon</h2>



Beyond contamination concerns, the authors highlight a subtler risk. Each year, the ocean pumps roughly a quarter of humanity’s carbon-dioxide emissions from the surface into the abyss. This happens chiefly via plankton that fix CO₂ and sink as aggregates or fecal pellets.



Plastic fragments of similar size and density could change how easily that biological “snow” sinks - or provide ballast that speeds some material downward while trapping carbon shallower than usual.



“Plastics may reduce the ocean’s ability to offset <a href="https://www.earth.com/news/ocean-climate-fixes-could-worsen-the-oxygen-crisis/">carbon dioxide</a>,” Stubbins said. A new $1.3-million <a href="https://www.nsf.gov/">National Science Foundation</a> project will probe that possibility by pairing vertical plastic profiles with carbon-flux measurements.



<h2 class="wp-block-heading" id="h-better-tools-for-deep-ocean-plastic">Better tools for deep ocean plastic</h2>



Documenting surface litter is straightforward: satellites, drones, and ships can skim the top meter with nets. Deep-water plastic work, by contrast, relies on expensive equipment and painstaking lab protocols.



The Northeastern team calls for an international push to harmonize depth-integrated sampling - particle size cuts, filtration volumes, and contamination controls. Standardizing these methods would allow global maps to be stitched together without relying on statistical guesswork.



“Plastics is an emergent field and there are concerns about how the changing physical environment of the deep ocean may have impacts on how the ocean functions as part of the Earth’s system,” Stubbins explained.



<h2 class="wp-block-heading" id="h-the-long-life-of-ocean-plastic">The long life of ocean plastic</h2>



Some countries are drafting binding treaties to curb plastic production and improve waste management. Yet even if global discharge stopped tomorrow, trillions of microplastics already in circulation would continue to drift, fragment, and sink to the bottom of the ocean for decades.



The new study provides a benchmark against which future surveys can measure progress - or lack thereof.



Policy, meanwhile, will need to target both ends of the life cycle: cutting single-use plastics at the source and investing in technologies to capture or biodegrade microplastics before they reach open water.



Until then, the ocean’s newly revealed plastic smog will remain a silent passenger in planetary processes that sustain climate stability and human <a href="https://www.earth.com/news/vaccinating-plants-could-boost-global-food-security/">food security</a>.



The study is published in the journal <a href="https://www.nature.com/articles/s41586-025-08818-1">Nature</a>.



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Ocean plastic crisis goes way deeper than we thought

A ten-year, nearly 2,000-station ocean survey has uncovered a diffuse...

Illustration,Concept,Of,A,Fleet,Of,Internet,Starlink,Satellites,In

Space is usually quiet at the frequencies that radio telescopes prize most. Over the last two years, however, scientists listening for whispers from the infant universe keep hearing radio signals from a loud new neighbor: SpaceX’s Starlink fleet.



<a href="https://staffportal.curtin.edu.au/staff/profile/view/steven-tingay-167822b3/" target="_blank" rel="noreferrer noopener">Steven Tingay</a> of Curtin University and the International Centre for Radio Astronomy Research (<a href="https://www.icrar.org/" target="_blank" rel="noreferrer noopener">ICAR</a>) led the team that traced the interference back to nearly 2,000 satellites using a prototype station of the Square Kilometre Array‑Low (<a href="https://www.skao.int/en/explore/telescopes/ska-low" target="_blank" rel="noreferrer noopener">SKA‑Low</a>) in Western Australia.



<h2 class="wp-block-heading" id="h-starlink-radio-noise-blocks-cosmic-signals">Starlink radio noise blocks cosmic signals</h2>



Radio telescopes hunt for the faint glow of <a href="https://arxiv.org/abs/2404.07250" target="_blank" rel="noreferrer noopener">neutral hydrogen</a>, a gas that filled space before the first stars switched on. Those signals arrive on Earth at strengths a thousand times weaker than a modern phone tower.



Even unplanned emissions from orbit can wipe them out. The survey found that unintended <a href="https://www.earth.com/news/largest-ever-map-of-the-universe-reveals-800000-galaxies/" target="_blank" rel="noreferrer noopener">satellite</a> leakage can match the brightest natural radio sources seen from Earth, which is enough to bury data at key hydrogen frequencies.



“It’s like taking the strongest sources in the sky and putting a bunch more artificial ones in, then making them move around a lot,” described Tingay.



<h2 class="wp-block-heading" id="h-desert-telescope-tracks-starlink-leaks">Desert telescope tracks Starlink leaks</h2>



The team pointed 256 dipole antennas across a 35‑meter (115-foot) patch of desert known for its radio silence. 



Across 29 days they recorded 2,446,692 full‑sky images spanning 24 frequencies between 73 and 235 megahertz.



Sophisticated software compared each snapshot with real‑time <a href="https://www.earth.com/news/thousands-of-galaxies-revealed-in-a-single-webb-image/" target="_blank" rel="noreferrer noopener">satellite</a> orbits. Every time a passing craft lined up with an unexpected spike in brightness, the program logged a hit.



By the end, 1,806 individual Starlink satellites, about 28 percent of the active constellation at the time, had betrayed a signal. 



Some appeared in nearly a third of all images captured at 170 megahertz, a band earmarked for early‑universe studies.



<h2 class="wp-block-heading" id="h-satellite-noise-outshines-natural-space-signals">Satellite noise outshines natural space signals</h2>



Two kinds of emissions dominated the log. 



Most <a href="https://www.earth.com/news/largest-cosmic-particle-cloud-ever-found-has-stunned-astronomers/" target="_blank" rel="noreferrer noopener">satellites</a> leaked a broadband hum across the entire 0.9‑megahertz window being measured. In addition, a smaller subset blasted a narrow, 13‑kilohertz tone every 100 seconds at 137.05 megahertz. 



Those pulses hit seven million janskys at the dish, outshining the Milky Way by orders of magnitude.



<a href="https://research.curtin.edu.au/cira/about-cira/our-people/" target="_blank" rel="noreferrer noopener">Dylan Grigg</a>, a Curtin University data specialist, noted that “the best way to stop this unintended emission is for the satellites to either reduce it or to stop it,” at the end of a long overnight observation run.



The International Telecommunication Union (<a href="https://www.itu.int/pub/R-HDB-22-2013" target="_blank" rel="noreferrer noopener">ITU</a>) reserves three slices of the spectrum, 73‑74.6, 150.05‑153, and 322‑328.6 megahertz, for <a href="https://public.nrao.edu/radio-astronomy/the-science-of-radio-astronomy/" target="_blank" rel="noreferrer noopener">radio astronomy</a>. 



Starlink leakage turned up in two of them, with 703 satellites detected in the lower protected band alone.



Because the rules govern only deliberate transmissions, no regulations are technically being broken. Yet the power difference between the leaks and the cosmic signals that astronomers seek can reach a factor of ten thousand.



<h2 class="wp-block-heading" id="h-reducing-starlink-radio-noise">Reducing Starlink radio noise</h2>



Starlink already dims its spacecraft in visible light by tipping solar panels away from Sun reflections. A similar hardware tweak, better shielding around onboard avionics, could muffle stray radio waves before they leave the bus.



Software filters on Earth offer a backup plan. Still, Tingay warns that erasing satellite noise in post‑processing may demand more computing power than the science analysis itself.



If hardware fixes prove impractical, operators could at least switch off problem components when passing above observatories. 



SpaceX already blanks its internet beams over major facilities; extending that courtesy to background electronics would help.



<h2 class="wp-block-heading" id="h-mega-constellations-and-future-astronomy">Mega‑constellations and future astronomy</h2>



Starlink is only the largest of several planned networks. Amazon’s Kuiper, <a href="https://oneweb.net/" target="_blank" rel="noreferrer noopener">OneWeb‑Eutelsat</a>, and <a href="https://spectrum.ieee.org/satellite-internet" target="_blank" rel="noreferrer noopener">China’s G60 project</a> each aim for thousands of craft in similar orbits.



Without new standards, the combined leakage could turn Earth’s low‑frequency sky into broadband static. 



That would cripple missions such as SKA‑Low’s quest to map the “<a href="https://www.earth.com/news/earthcares-first-year-surprising-climate-clues-unveiled-from-space/" target="_blank" rel="noreferrer noopener">cosmic</a> dawn,” when the first galaxies ignited about 13 billion years ago.



<h2 class="wp-block-heading" id="h-radio-astronomy-and-leaky-starlink">Radio astronomy and leaky Starlink</h2>



Astronomers have begun lobbying the ITU to extend protections to unintentionally radiated energy. Defining leakage limits, as already exists for consumer electronics on the ground, would give satellite makers a clear design target.



National spectrum agencies could then certify satellites before launch. Failing that, operators might face strict observing‑zone blackouts enforced by orbital debris tracking systems.



“The emissions are not regulated right now, but discussion has started,” Tingay said during the team’s briefing to Australian policymakers. He hopes the new data “provides the evidence base needed to move that process along.”



Time is tight. Starlink launches continue roughly once a week, with each <a href="https://www.spacex.com/vehicles/falcon-9/" target="_blank" rel="noreferrer noopener">Falcon 9</a> delivering up to 23 new units. Every fresh craft adds to the background haze, and older models show no sign of going quiet on their own. If action waits for the full 30,000‑satellite network, recovering a clean sky could be impossible.



Astronomy survived shortwave radio and television because engineers and regulators learned to share the dial. Whether low‑Earth orbit broadband joins that success story now rests on choices made in the next few years.



The study is published in <a href="https://arxiv.org/abs/2506.02831" target="_blank" rel="noreferrer noopener">Astronomy &amp; Astrophysics</a>.



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SpaceX’s Starlink satellites leak radio signals that threaten to ruin astronomy

Space is usually quiet at the frequencies that radio telescopes...

Nearly every modern gadget relies on metals that behave exactly as textbooks predict. Gallium refuses to play along. Nearly 150 years after French chemist <a href="https://en.wikipedia.org/wiki/Paul-%C3%89mile_Lecoq_de_Boisbaudran" target="_blank" rel="noreferrer noopener">Paul-Émile Lecoq de Boisbaudran</a> added the element to the periodic table, researchers are still sorting out why this silvery liquid shifts its personality when the heat is on. 



A spoon made of gallium will liquefy in a cup of tea, yet the same element anchors semiconductors, <a href="https://www.earth.com/news/floating-solar-panels-could-power-every-home-in-the-u-s/" target="_blank" rel="noreferrer noopener">solar panels</a>, and laser diodes that withstand scorching factory conditions.



For more than 30 years, physicists have wrestled with gallium’s structure in the liquid state. Competing studies have offered clashing explanations, especially around the role of <a href="https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/covalent-bond" target="_blank" rel="noreferrer noopener">covalent bonding</a> - a type of electron-sharing connection that metals rarely show. 



Fresh simulations have now stitched the puzzle pieces together and point to what scientists believe to be the decisive proof they've been searching for.



<h2 class="wp-block-heading" id="h-why-gallium-melts-early">Why gallium melts early</h2>



Gallium melts at 85 °F, far below the temperature of a warm summer day. That quirky transition happens because solid gallium forms tiny two-<a href="https://www.earth.com/news/hidden-chemistry-of-wine-what-actually-shapes-its-texture/" target="_blank" rel="noreferrer noopener">atom pairs</a> called dimers, and those pairs pack less densely than the liquid. The moment the dimers break apart, density rises and the metal flows. 



The story becomes stranger at higher heat. At temperatures well above the phase change, the dimers re-form, but not in ways scientists expected.



“Thirty years of literature on the structure of liquid gallium has rested on a fundamental assumption that is evidently not true,” says Professor Nicola Gaston of Waipapa Taumata Rau, <a href="https://www.auckland.ac.nz/en.html" target="_blank" rel="noreferrer noopener">University of Auckland</a>, and the <a href="https://www.macdiarmid.ac.nz/" target="_blank" rel="noreferrer noopener">MacDiarmid Institute</a> for Advanced Materials and Nanotechnology. 



Her team combined ab initio molecular-dynamics data with decades of experimental records to see how individual atoms mingle at several checkpoints on the thermometer.



<h2 class="wp-block-heading" id="h-liquid-gallium-myths-overturned">Liquid gallium myths overturned</h2>



Conventional wisdom held that <a href="https://www.earth.com/news/water-molecule-discovery-will-force-textbooks-to-be-rewritten/" target="_blank" rel="noreferrer noopener">covalent bonds</a> fade out once gallium liquefies and play only a minor role afterward. 



The fresh computational work shows the opposite: covalency matters more as the temperature climbs. In other words, the tighter electron sharing that disappears at 85 °F re-emerges and strengthens when the metal is pushed hundreds of degrees hotter.



The insight explains a long-standing electrical oddity. Gallium’s resistivity dips as it first passes the melting line - counter to most metals - then creeps upward in a nonlinear fashion. 



If covalent bonds regroup at elevated heat, they create a conduction bottleneck that raises resistivity, squaring experimental curves with <a href="https://www.earth.com/news/poorly-understood-force-helps-keep-atomic-nuclei-stable/" target="_blank" rel="noreferrer noopener">atomic-level theory</a>.



Textbook melting points depend on the tug-of-war between internal order and random motion. When the dimers dissolve, entropy shoots up, giving atoms the freedom to shift. 



That entropy spike accounts for gallium’s unusually low melt point without invoking mysterious bonding tricks at 85 °F. 



Once the liquid sits comfortably above the transition, the atomic sea settles just enough for bonds to snap back together - only this time within a looser, more disordered framework.



<h2 class="wp-block-heading" id="h-zinc-crystals-from-liquid-gallium">Zinc crystals from liquid gallium</h2>



Gallium’s renewed covalency at high temperatures also clarifies why the liquid can pull other metals into solution with minimal energy input. 



The shared-electron environment encourages elements such as <a href="https://www.earth.com/news/zinc-plays-an-overlooked-role-in-ocean-processes/">zinc</a>, copper, and tin to mix, forming room-temperature liquid alloys that engineers mold into stretchable circuits, heat-free solders, and microfluidic pumps.



A few years ago, researchers crystallized zinc inside a bath of molten gallium and watched delicate six-sided plates snowball outward. That project hinted at liquid gallium’s knack for directing complex shapes without external templates. 



The new structural roadmap shows that covalent rebonding supplies the subtle forces that align dissolved atoms as they solidify, making it easier to predict - and exploit - growth patterns.



Gallium-based liquids already act as catalysts that shuffle reactants into greener chemical pathways. The updated model will help chemists tune alloy recipes for faster charge transfer or sharper selectivity. 



In battery prototypes, thin films of gallium alloys spread across electrodes, filling microscopic cracks that normally kill capacity. Knowing when the liquid switches bonding modes could lengthen <a href="https://www.earth.com/news/scientists-created-carbon-14-battery-that-lasts-5700-years-without-a-recharge/">battery lifetimes</a> and lower manufacturing temperatures.



<h2 class="wp-block-heading" id="h-quirks-in-fabrication">Quirks in fabrication</h2>



Gallium’s solid compounds, including gallium arsenide and gallium nitride, drive radio-frequency amplifiers, high-brightness LEDs, and fast chargers. 



Fabricating those compounds sometimes involves droplets of pure gallium that remove heat or transport precursor atoms. 



Process engineers need precise viscosity, density, and conductivity data at every stage, and the re-emergence of covalent links at high heat feeds directly into those parameters.



Understanding gallium’s behavior also safeguards supply chains. The metal is mined as a by-product of <a href="https://www.earth.com/news/exposing-the-hidden-climate-costs-of-everyday-materials/">aluminum production</a>, mainly from bauxite ore. 



Global output hovers around 460 tons per year, and demand surges whenever display or photovoltaic markets expand. Tailoring alloys that use less gallium, yet keep its liquid perks, will ease strain on future inventories.



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



Beyond Earth, gallium could help planetary scientists sniff out ancient microbes. Because the element forms stable bonds with <a href="https://www.earth.com/news/moon-volcanoes-left-sparkling-clues-behind-in-form-of-tiny-glass-beads/">oxygen and sulfur</a>, it may lock biosignatures into Martian rock layers. 



Some geochemists argue that gallium traces could outlast fragile carbon compounds, providing a longer-lived clue to life. The revamped structural picture supplies the chemical logic behind that durability.



As liquid metals step into flexible electronics, soft robotics, and low-carbon chemistry, knowing exactly how gallium’s atoms dance under heat will pay dividends.



Gallium still bends spoons for party tricks, but its greater trick lies in how a simple temperature dial rewrites atomic rules. 



By showing where covalent bonds vanish and return, the research clears fog from a field that fuels countless technologies, from phone screens to satellite links. 



The full study was published in the journal <a href="https://pubs.rsc.org/en/content/articlelanding/2024/mh/d4mh00244j/unauth" target="_blank" rel="noreferrer noopener">Materials Horizons</a>.



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Previously unknown properties of a very unusual metal challenge a 150-year-old assumption

Nearly every modern gadget relies on metals that behave exactly...

Steel is the skeleton of modern life, yet the iron that makes it has a backstory far older than the first nail. For decades, geologists thought the world's richest and largest iron ore deposits formed not long after breathable oxygen spread through Earth’s air some 2.2 billion years ago.



Fresh evidence now knocks that timing sideways, suggesting the world-class reserves in the <a href="https://www.researchgate.net/figure/Simplified-geological-map-of-the-Hamersley-Province_fig1_366035930" target="_blank" rel="noreferrer noopener">Pilbara’s Hamersley Province</a> of Australia are about 1.4 to 1.1 billion years younger than previously believed.



The billion-year gap isn’t a rounding error - it reshapes both scientific thinking and <a href="https://www.earth.com/news/chinas-rare-earth-jackpot-1-15-million-tons-of-minerals-uncovered/" target="_blank" rel="noreferrer noopener">mining strategy</a>.



Across the red plains east of the coastal town of Karratha, open-pit mines peel back ancient rock like pages in a weather-worn diary. Their iron feeds furnaces from Indiana to India. 



Western Australia alone supplied 38 percent of global iron ore in 2023, far out-muscling every other region on the planet.



<h2 class="wp-block-heading" id="h-a-1-3-billion-year-iron-ore-correction">A 1.3 billion-year iron ore correction</h2>



<a href="https://www.earth.com/earthpedia-articles/what-the-heck-is-iron-ore/" target="_blank" rel="noreferrer noopener">Hematite</a>, the lustrous mineral that drives these operations, occasionally traps a whisper of uranium inside its lattice. That radioactive speck decays into lead at a steady pace, letting scientists read the mineral’s “birth certificate.” 



Using that method, Dr. Liam Courtney-Davies and colleagues from <a href="https://www.curtin.edu.au/" target="_blank" rel="noreferrer noopener">Curtin University</a> dated crystals from every major banded iron formation in the Hamersley. Their clock pointed stubbornly to a younger era, long after the <a href="https://www.earth.com/news/it-took-200-million-years-for-earth-to-get-its-oxygen/" target="_blank" rel="noreferrer noopener">Great Oxidation Event</a>. 



“The energy from this epic geological activity likely triggered the production of billions of tons of iron-rich rock across the Pilbara,” Dr. Courtney-Davies said.



The team’s timeline ties high-grade ore to a stretch when the <a href="https://www.sciencedirect.com/science/article/abs/pii/S1342937X17300485" target="_blank" rel="noreferrer noopener">supercontinent Columbia</a> had ripped apart and new continental mash-ups were brewing. 



Crustal plates heaved, mountains rose, and faults opened, pumping hot, oxygen-laden fluids through pre-existing iron beds. 



Those fluids stripped out silica, leaving hematite that tops 60 percent iron - twice the grade of the original sea-floor rust.



<h2 class="wp-block-heading" id="h-how-tectonics-forged-treasure">How tectonics forged treasure</h2>



Plate motion rarely draws headlines, yet its fingerprints sit on everything from fossil-fuel reservoirs to <a href="https://www.earth.com/news/geologists-discover-the-largest-copper-gold-and-silver-deposit-in-the-last-three-decades/" target="_blank" rel="noreferrer noopener">copper belts</a>. The Hamersley story adds one more chapter: bulk commodities. 



Associate Professor Martin Danišík, part of the Curtin University group, noted, “Our research indicates these deposits formed in conjunction with major tectonic events, highlighting the dynamic nature of our planet’s history and the complexity of iron ore mineralization.”



Before that remark, his team spelled out the scale of the upgrade. 



“Until now, the exact timeline of these formations changing from 30 percent iron as they originally were, to more than 60 percent iron as they are today, was unclear, which has hindered our understanding of the processes that led to the formation of the world's largest ore deposits,” Danišík continued.



Their solution - a fine-point uranium-lead probe inside single grains - sidesteps the guesswork of dating surrounding rocks.



<h2 class="wp-block-heading" id="h-how-this-helps-iron-ore-miners">How this helps iron ore miners</h2>



Age is more than trivia. If a deposit formed in a tectonic “sweet spot” 1.3 billion years ago, explorers can hunt elsewhere for the same recipe: ancient banded iron reworked by heat and fluid flow during that window. 



In practice, that means following suture zones and <a href="https://www.earth.com/news/most-dangerous-part-of-this-west-coast-earthquake-fault-cascadia-subduction-zone/" target="_blank" rel="noreferrer noopener">fault corridors</a> that lit up when Columbia fell apart and its successor, Rodinia, took shape.



For the industry, timing meets money. The value of Western Australia’s iron ore exports hit $136 billion in the 12 months to June 2024, with China absorbing about four-fifths of that haul. 



Federal forecasters expect Australia’s iron ore earnings to fall to about $107 billion in 2024–25 as prices retreat. Efficiency matters when margins tighten, so guidance on where to drill next carries real weight.



<h2 class="wp-block-heading" id="h-fluid-highways-in-ancient-rock">Fluid highways in ancient rock</h2>



To grasp why fluids matter, picture an interstate highway system beneath solid rock - not a puddle here or there, but branching paths that cut through thousands of feet of crust. 



When supercontinents crunch or tear, pressure and heat send chemically rich water racing along those paths. 



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/06/iron-ore_deep-blue_Hamersley-Province-Map_credit-Curtin-University_1m.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/06/iron-ore_deep-blue_Hamersley-Province-Map_credit-Curtin-University_1s.webp" alt="Geologic map of the Pilbara craton with sample locations marked by blue stars (Left). Stratigraphic column (Right) showing the Hamersley Group, which hosts all martite-microplaty hematite deposits and overlying groups hosting hematite ore clasts. Credit: Curtin University" class="wp-image-1974248"/></a><figcaption class="wp-element-caption">Geologic map of the Pilbara craton with sample locations marked by blue stars (Left). Stratigraphic column (Right) showing the Hamersley Group, which hosts all martite-microplaty hematite deposits and overlying groups hosting hematite ore clasts. Click image to enlarge. Credit: Curtin University</figcaption></figure>



In the Pilbara, such pulses ferried extra oxygen, converting magnetite and siderite into hematite far purer than the original mix. 



Those same highways are visible in other cratons, from Brazil’s Quadrilátero Ferrífero to India’s Singhbhum region, hinting that younger ages could emerge elsewhere once geochronologists put them under the microscope.



<h2 class="wp-block-heading" id="h-economic-iron-ore-ripples">Economic iron ore ripples</h2>



Global <a href="https://www.earth.com/news/decarbonizing-worlds-industrial-emissions-possible-with-current-technology/" target="_blank" rel="noreferrer noopener">steel demand</a>, already recovering after pandemic doldrums, is forecast to edge up 1.2 percent to about 1.815 billion metric tons in 2025. 



Meeting that appetite without <a href="https://www.earth.com/news/chatgpts-carbon-footprint-is-astronomical-and-not-sustainable/" target="_blank" rel="noreferrer noopener">ballooning emissions</a> pushes producers toward higher-grade feedstock; richer ore needs less coke per ton of metal. Western Australia’s stash, upgraded by billion-year-old fluids, stands out in that carbon calculus.



Green-steel projects now pepper feasibility studies on three continents. Australia believes converting its ore into hydrogen-reduced “green iron” before shipping could more than double export value - potentially topping $250 billion a year. 



While those numbers rely on policy shifts and infrastructure build-outs, the geologic backstory underpins the commercial lure: ore that almost smelts itself.



<h2 class="wp-block-heading" id="h-the-detective-work-never-ends">The detective work never ends</h2>



“By using an emerging technique to date <a href="https://www.earth.com/news/phantom-nutrient-the-secret-force-that-fuels-plant-growth/" target="_blank" rel="noreferrer noopener">iron oxide minerals</a> through uranium and lead isotope analysis within the mineral grains, we directly dated all the major giant BIF-hosted iron ore deposits in the Hamersley Province.” 



That line from the research team reads like a footnote, yet it signals a methodological leap. Asking the rocks directly, rather than their neighbors, can overturn decades of assumption in a single lab session.



“The discovery of a link between these giant iron ore deposits and changes in supercontinent cycles enhances our understanding of ancient geological processes and improves our ability to predict where we should explore in the future.” 



With that, Dr. Courtney-Davies closes the loop between academic insight and drill-bit decisions. The story of iron is still being written, one crystal at a time.



The full study was published in the journal <a href="https://www.pnas.org/doi/10.1073/pnas.2405741121" target="_blank" rel="noreferrer noopener">Proceedings of the National Academy of Sciences</a>.



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Scientists studying Earth's largest iron ore deposits uncover a 1.3-billion-year-old secret

Steel is the skeleton of modern life, yet the iron...

Every year, mosquito-borne diseases cut short more than a million lives across the globe, outpacing every other animal threat to humanity. The rising toll has public-health teams scrambling for fresh combat tools, especially as traditional chemical sprays lose their edge.



That loss stems from two hard truths. First, the very <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC7692614/" target="_blank" rel="noreferrer noopener">pyrethroid insecticides</a> that once worked wonders now linger in soil and water, nudging delicate ecosystems off balance. 



Second, mosquitoes adapt fast. Larvae soaking in tainted puddles and adults drifting through treated neighborhoods increasingly shrug off doses that once killed them. 



<a href="https://www.earth.com/news/mosquito-repellents-that-actually-work-yes-thanks-to-ai-machine-learning/" target="_blank" rel="noreferrer noopener">Controlling the pests</a> at their waterborne stage is vital, yet options that stay potent without harming everything else remain limited.



<h2 class="wp-block-heading" id="h-cannabis-cbd-and-mosquitoes">Cannabis, CBD, and mosquitoes</h2>



Recent research published in the journal Insects points to a solution hiding in plain sight: the hemp plant, Cannabis sativa. 



After air-drying and grinding ordinary hemp leaves, scientists at <a href="https://www.osu.edu/" target="_blank" rel="noreferrer noopener">The Ohio State University</a> led by Erick Martinez Rodriguez extracted <a href="https://www.earth.com/news/cbd-reduces-the-unwanted-side-effects-of-thc/" target="_blank" rel="noreferrer noopener">cannabidiol (CBD)</a> and added the concentrate to cups of water teeming with yellow fever mosquito larvae. 



Within 48 hours, both a strain that laughs at <a href="https://www.earth.com/news/rising-temperatures-could-make-insect-repellents-less-effective/" target="_blank" rel="noreferrer noopener">common insecticides</a> and a non-resistant strain were wiped out.



“Mosquitoes are one of the deadliest animals in the world, mainly because as adults they serve as vectors of disease,” Rodriguez explained.



<h2 class="wp-block-heading" id="h-from-resistance-to-vulnerability">From resistance to vulnerability</h2>



Two important findings jumped out. The first was total mortality: every mosquito larva exposed to sufficient CBD died by the two-day mark, regardless of <a href="https://www.earth.com/news/scientists-learn-how-mosquitoes-use-sound-to-outsmart-and-evade-human-defenses/" target="_blank" rel="noreferrer noopener">its genetic armor</a>. 



The second was efficiency. While industrial chemicals often push resistance higher with every generation, CBD’s effect cut straight through those defenses. Doses varied, but even modest concentrations proved lethal to all mosquito larvae.



“If you compare the amount of hemp extract needed to kill 50 % of the population to other synthetic conventional insecticides, it is on the high side, but when you compare it side by side to other natural extracts we have tested in our lab, only a relatively low amount is required to produce high mortality values in larvae,” said Martinez Rodriguez.



<h2 class="wp-block-heading" id="h-how-cbd-kills-mosquitoes">How CBD kills mosquitoes</h2>



Chemical sleuthing showed that CBD dominated the hemp extract, and terpene fractions did little damage on their own. 



Larvae were judged dead once they stopped moving under a gentle nudge, confirming the cannabinoid’s direct impact on vital systems.



Insects lack the endocannabinoid receptors that give <a href="https://www.earth.com/news/cbd-can-help-ease-chronic-pain-anxiety-and-mood-disorders/" target="_blank" rel="noreferrer noopener">CBD its wellness reputation</a> among humans, so the compound must strike different molecular targets - possibly ion channels that govern nerve impulses or enzymes tied to muscle control. 



Whatever the route, CBD skirts the metabolic tricks that shield many larvae from pyrethroids.



<h2 class="wp-block-heading" id="h-hemp-economics-meet-public-health">Hemp economics meet public health</h2>



Hemp is no niche crop. U.S. farmers planted about 27,680 acres in 2023, and the total value of <a href="https://www.earth.com/news/hemp-seeds-could-be-a-game-changer-as-an-alternative-protein-source/" target="_blank" rel="noreferrer noopener">hemp products</a> topped $291 million.



Leaves, often left as low-value waste after flowers and seeds are harvested, could become raw material for larvicides. 



Turning those leaf cast-offs into mosquito-control pellets would give growers an extra revenue stream while trimming refuse piles.



The crop’s adaptability sweetens the deal. Hemp thrives across a wide climate range, grows quickly, and rarely needs harsh pesticides of its own. 



Rural communities looking to diversify incomes and urban growers cultivating indoor micro-hemp could both feed a supply chain aimed at vector-control programs from Texas to Tanzania.



<h2 class="wp-block-heading" id="h-strains-and-waterway-safety">Strains and waterway safety</h2>



Field trials must still answer hard questions: How long does CBD linger in ponds? Does it bother tadpoles, fish fry, or helpful insects? 



Early lab work hints at selectivity, yet natural habitats are complex. Regulators will demand data showing that CBD pellets, briquettes, or slow-release films silence mosquito larvae without tipping aquatic ecosystems.



A second layer of testing will match different hemp strains for efficacy. Plants bred for fiber deliver more stalk than cannabinoid, while floral varieties boast <a href="https://pubchem.ncbi.nlm.nih.gov/compound/Cannabidiol" target="_blank" rel="noreferrer noopener">richer CBD profiles</a>. 



Selecting cultivars that maximize larvicidal punch and minimize unwanted compounds will keep costs down and environmental margins wide.



<h2 class="wp-block-heading" id="h-next-steps-for-cbd-and-mosquito-control">Next steps for CBD and mosquito control</h2>



Scientists plan to refine dosage, explore formulations that stick to the water’s surface, and probe how CBD interacts with other biocontrol measures like Bacillus thuringiensis israelensis. Combining modes of action could slow resistance even further. 



Teams will also map out manufacturing pipelines - picture hemp-leaf extract concentrated at regional facilities, then shipped as shelf-stable granules to <a href="https://www.earth.com/news/why-some-people-are-mosquito-magnets/" target="_blank" rel="noreferrer noopener">mosquito-control districts</a>.



Policy makers, meanwhile, need clear guidelines. Approving a botanical larvicide means balancing urgent disease threats against conservation goals. Transparent monitoring and community engagement will help keep public trust.



<h2 class="wp-block-heading" id="h-another-weapon-in-the-mosquito-wars">Another weapon in the mosquito wars</h2>



Hemp-derived CBD will not single-handedly end malaria, dengue, or Zika. Yet the discovery that a familiar wellness compound doubles as a larval assassin widens the playbook. 



By uniting agriculture, chemistry, and entomology, researchers have opened <a href="https://www.earth.com/news/mosquito-habitats-are-expanding-due-to-climate-change/" target="_blank" rel="noreferrer noopener">a practical path</a> toward safer mosquito control. 



If larger-scale tests confirm the promise seen in the lab, those humble hemp leaves could soon guard countless backyard birdbaths, drainage ditches, and rice paddies - one cup of water at a time.



The full study was published in the journal <a href="https://www.mdpi.com/2075-4450/15/7/517" target="_blank" rel="noreferrer noopener">Insects</a>.



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Cannabis extract proves to be highly effective at killing the most dangerous animals in the world

Every year, mosquito-borne diseases cut short more than a million...

From corporate boards to honeybee hives and ants colonies, groups tend to follow the majority. But biologists and social scientists have found that a vocal minority - sometimes just 5 to 10 percent - can sway the final decision if they’re persuasive, energized, or well-connected. This effect is known as “minority influence.”



A new study shows that <a href="https://www.earth.com/news/fire-ants-can-teach-us-how-to-create-stronger-materials/" target="_blank" rel="noreferrer noopener">fire ants</a> offer a dramatic, gene-driven version of the same principle. A handful of workers carrying a particular stretch of&nbsp;“<a href="https://www.earth.com/news/selfish-dna-transposons-control-early-human-development-not-genes/" target="_blank" rel="noreferrer noopener">selfish DNA</a>” can push their nest-mates to welcome extra queens, transforming the colony’s entire social order.



<h2 class="wp-block-heading" id="h-selfish-dna-and-ant-colony-structure">Selfish DNA and ant colony structure</h2>



The invasive red imported fire ant, Solenopsis invicta, dominates swaths of the southeastern United States and is spreading on multiple continents. 



Ecologically and economically, it is one of the most impactful insects on Earth. It also comes in two distinct social forms.



Single-queen colonies (monogyne) recognize and defend one egg-laying monarch. Workers in these nests are intensely territorial, killing any foreign queen that dares enter.



Multiple-queen colonies (polygyne) tolerate several unrelated <a href="https://www.earth.com/news/ant-queens-turn-to-cannibalism-recycle-bodies-for-colony-disease-control/" target="_blank" rel="noreferrer noopener">queens</a> and spread by budding - new queens and escorts walk a short distance and start satellite nests.



The social form matters: monogyne nests are aggressive but slower to spread; polygyne nests can carpet landscapes with interconnected supercolonies.



A single gene complex, dubbed Gp-9, largely decides whether a colony embraces one queen or many. The variant known as Gp-9 B promotes single-queen structure; the variant Gp-9 b pushes toward multiple queens.



Only workers with the b allele accept extra royalty - and that gene acts in strikingly “selfish” fashion, ensuring its own propagation.



<h2 class="wp-block-heading" id="h-genetic-roots-of-ant-behavior">Genetic roots of ant behavior</h2>



Takao Sasaki, now an associate professor in the <a href="https://www.sas.rochester.edu/bcs/" target="_blank" rel="noreferrer noopener">University of Rochester’s Department of Brain and Cognitive Sciences</a>, teamed with postdoctoral researcher Haolin Zeng and Professor Kenneth Ross at the <a href="https://www.uga.edu/" target="_blank" rel="noreferrer noopener">University of Georgia</a>. Together, they tested how small a minority of b-bearing workers could tip an entire colony.



Most previous work had examined stable nests already committed to one form or the other. The new experiments created mixed groups from scratch, mirroring the early stages of an invasion when different ant lineages collide.



“Our research may help us understand how other animals make consensus decisions,” Sasaki said.



Using DNA markers, the team first verified each ant’s social-genotype - B B for single-queen preference or B b for multiple-queen preference. They then built experimental colonies of 3,000 workers and a single B-type queen.



Into these colonies they introduced B b workers in varying proportions, from zero to 30 percent, along with test queens carrying either genotype. Continuous video monitored how workers treated potential newcomers.



<h2 class="wp-block-heading" id="h-dna-can-shift-the-ant-colony">DNA can shift the ant colony </h2>



With no B b workers present, resident ants killed any stranger queen in the colony within hours, matching monogyne behavior in the wild. But once the minority of B b workers reached roughly 10 percent, the colony’s stance softened.



Those few workers began grooming and feeding extra queens that carried the same b allele, escorting them safely into the brood chambers. 



Over the following days, B B workers joined the caretaking - even though the shift ultimately lowers their own inclusive fitness. The single-queen colony had morphed into a multi-queen society, simply because a genetic minority rewrote the ground rules.



“By looking at their genes, we know their preferences for having one queen versus multiple queens,” Sasaki said. “By manipulating the proportion of <a href="https://www.earth.com/news/larger-ant-colonies-drove-the-evolution-of-worker-castes/" target="_blank" rel="noreferrer noopener">workers</a> with certain genes, we can test if and how a minority can convince the rest of the group members.”



Chemical communication is the likely mechanism. Fire ants rely on pheromones to tell friend from foe and to decide which queens belong.



Additional tests showed b-bearing workers alter queen pheromones or change how nest-mates respond to those chemical signals. Whichever the pathway, the outcome favors any queen - and thus any gene - matching the minority’s genotype.



<h2 class="wp-block-heading" id="h-selfish-dna-shapes-behavior">Selfish DNA shapes behavior</h2>



The study highlights an evolutionary twist known as an indirect genetic effect: one individual’s traits are molded not just by its own DNA and environment, but by the genes carried by its social partners.



Here, the selfish DNA in roughly a tenth of the ants drives an outcome (polygyne structure) that benefits copies of that same element, even though it may not help the colony at large.



“This knowledge is important not only for understanding the biology of social insects like fire ants but also for broader insights into the evolution of cooperation and <a href="https://www.earth.com/news/survival-of-the-friendliest-social-animals-live-longer/" target="_blank" rel="noreferrer noopener">sociality</a> in animals, including humans,” Zeng said.



Because multi-queen colonies bud readily and thus expand invasion fronts, the ability of a genetic minority to flip nest behavior could accelerate the spread of fire ants worldwide. Evolutionary models will need to account for such feedback between genes and group dynamics.



<h2 class="wp-block-heading" id="h-ants-think-like-neurons">Ants think like neurons</h2>



Sasaki frames the findings in terms of “collective cognition,” his broader research focus. Just as neurons exchange signals to create unified thoughts, social insects exchange chemical and tactile cues to make group decisions.



If a small cluster of neurons can trigger a mental state, why not a small cluster of genetically distinct ants triggering a social state?



“The brain is a good example,” Sasaki explained. “Each neuron talks to other neurons. A brain is a cognitive unit. Ants as colonies make collective decisions like brains do.”



<h2 class="wp-block-heading" id="h-genes-help-outvote-majority-rule">Genes help outvote majority rule</h2>



The fire-ant case suggests that minority influence may have a deeper biological foundation than previously realized. In some cases, it’s encoded in selfish stretches of DNA that manipulate social systems like ant colonies from within.



Whether similar elements lurk in other species, subtly guiding flock movements, pack hierarchies, or even aspects of human <a href="https://www.earth.com/news/secret-social-lives-pandas-have-their-own-version-of-facebook/" target="_blank" rel="noreferrer noopener">social networks</a>, remains an open question.



What is clear is that in complex societies, majority rule is never absolute: under the right genetic and social conditions, the few can still lead the many.



The study is published in the journal <a href="https://www.pnas.org/doi/10.1073/pnas.2501740122">Proceedings of the National Academy of Sciences</a>.



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'Selfish DNA' can result in minority influence in social animal groups, including humans

From corporate boards to honeybee hives and ants colonies, groups...

The disappearance of South America’s mastodons some ten millennia ago did more than erase a charismatic animal; it severed an ancient partnership that once spread the seeds of large-fruited trees across the continent.



A new study shows that these elephant-like creatures were habitual fruit-eaters and indispensable couriers of botanical life. This helps explain why several modern tree species now teeter on the brink of extinction.



An international research team examined ninety-six fossil molars of Notiomastodon platensis collected along a 1,500-kilometer sweep of Chilean coastline.



Using microscopic wear patterns, chemical fingerprints locked in <a href="https://www.earth.com/news/tooth-enamel-analysis-suggests-early-eurasians-were-multiple-species-paranthropus-robustus/" target="_blank" rel="noreferrer noopener">tooth</a> enamel, and residues trapped in dental calculus, they pieced together the animal’s menu.



<h2 class="wp-block-heading" id="h-fossil-traces-reveal-fruit-diet">Fossil traces reveal fruit diet</h2>



Florent Rivals is a researcher at the Catalan Institute for Human Palaeoecology and Social Evolution (<a href="https://cerca.cat/en/centres-cerca/iphes/" target="_blank" rel="noreferrer noopener">IPHES-CERCA</a>).



“We found starch residues and plant tissues typical of fleshy fruits, such as those of the Chilean palm (Jubaea chilensis),” he said.



Those tiny traces, preserved since the Pleistocene, provide the first direct evidence that the <a href="https://www.earth.com/news/student-discovers-a-34000-year-old-mastodon-fossil-by-accident-while-walking-around-a-farm/">mastodon</a> routinely swallowed whole fruit - and by extension the seeds buried inside.



Stable-isotope signatures reinforced the picture. “Through stable isotope analysis, we were able to reconstruct the animals’ environment and diet with great precision,” said Iván Ramírez-Pedraza, a researcher at IPHES-CERCA who helped chart the chemical trail.



The pattern points to a mixed woodland rich in fruit resources, the kind of landscape where a multi-ton mammal could feast while roaming long distances.



<h2 class="wp-block-heading" id="h-testing-a-forty-year-old-idea"><a></a>Testing a forty-year-old idea</h2>



Back in 1982, biologist Daniel Janzen and paleontologist Paul Martin suggested that many tropical trees evolved oversized, sugary fruits specifically to lure now-extinct megafauna.



These included mastodons, giant <a href="https://www.earth.com/news/lost-world-of-giant-sloths-why-did-they-shrink-and-when-did-it-happen/" target="_blank" rel="noreferrer noopener">sloths</a>, and native horses - animals capable of gulping down the bounty and depositing viable seeds far from the parent plant.



Their “neotropical anachronism” hypothesis was ingenious but largely speculative. The new study supplies the hard proof those pioneers lacked.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/06/mastodons_Notiomastodon-platensis_chile_diversity_credit-Mauricio-Alvarez_1m.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/06/mastodons_Notiomastodon-platensis_chile_diversity_credit-Mauricio-Alvarez_1s.webp" alt="Diversity of extinct mammals that inhabited the surroundings of Ancient Lake Tagua Tagua. Credit: Mauricio Álvarez" class="wp-image-1974219"/></a><figcaption class="wp-element-caption">Diversity of extinct mammals that inhabited the surroundings of Ancient Lake Tagua Tagua. Click image to enlarge. Credit: Mauricio Álvarez</figcaption></figure>



Lead author Erwin González-Guarda of the <a href="https://www.uoh.cl/" target="_blank" rel="noreferrer noopener">University of O’Higgins</a> argued that the multi-proxy approach was crucial.



Conventional wear studies alone cannot distinguish leaves from soft fruit, while isotopes reveal diet breadth but not specific ingredients. Residual microfibers in dental plaque filled that gap, confirming that fruit made up a regular part of the mastodon’s meals.



<h2 class="wp-block-heading" id="h-mastodons-spread-forest-seeds">Mastodons spread forest seeds</h2>



“Dental chemistry gives us a direct window into the past,” said co-author Carlos Tornero, an isotope specialist at IPHES-CERCA.



The team concludes Notiomastodon was a key long-distance seed disperser in late Pleistocene South America.



When the animals died out - probably under combined pressure from rapid <a href="https://www.earth.com/news/ancient-climate-shift-sheds-light-on-future-global-warming/" target="_blank" rel="noreferrer noopener">climate shifts</a> and expanding human hunting - no substitute of equal size and wanderlust remained.



Tapirs, peccaries, and monkeys still disperse some fruit in tropical zones, but across central Chile, the ecological courier service is effectively bankrupt.



<h2 class="wp-block-heading" id="h-forests-feel-the-absence">Forests feel the absence</h2>



The researchers ran a machine-learning analysis to gauge present-day risk for plants once dependent on megafaunal dispersers.



In central Chile, forty percent of those trees now sit on threatened or endangered lists - four times the proportion in regions where alternative animal carriers survive.



“Where that ecological relationship between plants and animals has been entirely severed, the consequences remain visible even thousands of years later,” said co-author Andrea P. Loayza, paleontologist at the Institute of Ecology and Biodiversity (<a href="https://ieb-chile.cl/en/" target="_blank" rel="noreferrer noopener">IEB</a>) in Chile.



Today the Chilean palm endures in a few fragmented groves. The monkey-puzzle tree, Araucaria araucana, iconic yet genetically impoverished, clings to high Andean ridges.



The gomortega, Gomortega keule, known locally as queule, hangs on in scattered coastal valleys. Its plum-sized fruit now mostly drops beneath the parent canopy, rather than being hauled kilometers away inside a mastodon’s gut.



<h2 class="wp-block-heading" id="h-forests-seeds-and-mastodons">Forests, seeds, and mastodons</h2>



Beyond its detective work, the paper carries a cautionary message. Ecosystems retain the impact of lost species for millennia, and restoring their roles will be a major challenge.



Rewilding with living <a href="https://www.earth.com/news/large-herbivores-are-not-always-harmful-in-new-territories/" target="_blank" rel="noreferrer noopener">large herbivores</a> has been floated as one possibility, and the fresh Chilean data offer a benchmark for choosing modern analogues based on diet and ranging behavior, not just body mass.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/06/mastodons_Notiomastodon-platensis_paleoenvironment-chile_credit-Mauricio-Alvarez_1m.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/06/mastodons_Notiomastodon-platensis_paleoenvironment-chile_credit-Mauricio-Alvarez_1s.webp" alt="Reconstruction of the paleoenvironments in which Chilean mastodons lived, from the semi-arid north to the cold rainforests of Patagonia. Credit: Mauricio Álvarez" class="wp-image-1974221"/></a><figcaption class="wp-element-caption">Reconstruction of the paleoenvironments in which Chilean mastodons lived, from the semi-arid north to the cold rainforests of Patagonia. Click image to enlarge. Credit: Mauricio Álvarez</figcaption></figure>



“By combining different lines of evidence, we’ve been able to robustly confirm their frugivory and the key role they played in these ecosystems,” Tornero emphasized.



Conservation managers might use such findings to prioritize corridors that allow surviving mammals to move seeds. They could also experiment with human-mediated dispersal for tree species marooned by the mastodon’s absence.



<h2 class="wp-block-heading" id="h-old-bones-new-purpose">Old bones, new purpose</h2>



“Paleontology isn’t just about telling old stories,” Rivals concluded. “It helps us recognize what we’ve lost - and what we still have a chance to save.”



With climate change and habitat fragmentation tightening their grip, lessons from deep time may guide present-day action.



Protecting and, where possible, mimicking the ancient partnership between fruit-bearing trees and their gigantic gardeners could give endangered South American forests a second shot at resilience.



The study is published in the journal <a href="https://www.nature.com/articles/s41559-025-02713-8" target="_blank" rel="noreferrer noopener">Nature Ecology &amp; Evolution</a>.



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Mastodon extinction is still causing problems with South American ecosystems

The disappearance of South America’s mastodons some ten millennia ago...

Antarctic krill - the shrimp-like crustaceans that feed whales, seals, and penguins - sit at the heart of the Southern Ocean food web. Yet these tiny animals are also the target of a fast-growing commercial fishery.



A new study led by the <a href="https://www.awi.de/en/" target="_blank" rel="noreferrer noopener">Alfred Wegener Institute</a> (AWI) and the <a href="https://www.hi.no/hi/en" target="_blank" rel="noreferrer noopener">Norwegian Institute of Marine Research</a> used more than 30,000 hours of sonar recordings from krill-trawling vessels. 



The analysis pinpointed when and where fishing fleets overlap with natural krill predators. The results highlight seasonal hotspots of competition that managers can no longer afford to ignore.



<h2 class="wp-block-heading" id="h-using-sonar-for-krill-clues">Using sonar for krill clues</h2>



Fishing vessels routinely run powerful echo sounders to locate krill swarms. By repurposing those same acoustic logs, scientists gained an unprecedented view of the submarine “traffic” beneath the ships.



The team analyzed over 30,000 hours of sonar data from three krill fishing vessels, gathered over six years in the Southern Ocean. Machine learning algorithms filtered the files for the distinctive signatures produced when <a href="https://www.earth.com/news/whales-blow-bubble-smoke-rings-near-humans-to-communicate/" target="_blank" rel="noreferrer noopener">whales</a>, penguins, or seals dive under a vessel.



“During such encounters, ships and krill predators pursue the same krill swarms," said lead author Dominik Bahlburg, a scientist at AWI. 



"This allowed us to analyze the spatial and temporal dynamics of this competition in order to identify locations and time periods where the interaction between the two groups is particularly intensive."



<h2 class="wp-block-heading" id="h-where-penguins-seals-and-trawlers-converge"><a></a>Where penguins, seals, and trawlers converge</h2>



Patterns emerged once the detections were mapped. <a href="https://www.earth.com/news/penguins-are-threatened-by-mercury-contamination/" target="_blank" rel="noreferrer noopener">Penguins</a> and fur seals appeared alongside fishing gear in both summer and winter, especially around the South Orkney Islands and South Georgia. 



Whales appeared most near the Antarctic Peninsula in autumn, when they fatten for their long migration north.



“The South Orkney Islands seem to be a real hotspot for encounters with penguins,” Bahlburg said. “Compared to the Antarctic Peninsula, they have received far less attention in the debate on the impact of krill fishing and many of the colonies affected there are currently not regularly monitored.”



<h2 class="wp-block-heading" id="h-direct-competition-with-penguins">Direct competition with penguins</h2>



The overlap is worrisome as trawlers fish near breeding colonies when adult birds must feed their chicks. Voluntary buffer zones aimed to ease this conflict, but sonar evidence reveals an unintended side effect.



This also suggests that fishing vessels continue to encounter penguins despite the voluntary restriction zones around the Antarctic Peninsula. 



The vessels also continue to compete directly with penguins for krill during the breeding season. Instead, the pressure appears to have shifted to the South Orkney Islands.



<h2 class="wp-block-heading" id="h-fishing-overlaps-persist-in-winter">Fishing overlaps persist in winter</h2>



One assumption had been that moving effort into winter - when breeding pressures ease - would spare <a href="https://www.earth.com/news/human-noise-is-disrupting-wildlife-in-antarctica/" target="_blank" rel="noreferrer noopener">wildlife</a>. The new data challenge that view.



“We were able to show that fisheries and penguins as well as fur seals encounter each other just as frequently in the winter as in the summer season,” Bahlburg said.



Since animals roam farther from colonies in winter, the persistence of close encounters surprised the authors and may require a reassessment.



While penguins and seals were encountered less often near the Peninsula, autumn fishing there overlapped heavily with whales. These whales depend on krill to build blubber reserves before migrating to equatorial calving grounds.



<h2 class="wp-block-heading" id="h-krill-fleet-data-goes-public">Krill fleet data goes public</h2>



The team found little year-to-year fluctuation in their maps. “Remarkably, these patterns were quite stable for <a href="https://www.earth.com/news/elephant-seals-provide-a-window-into-the-oceans-twilight-zone/" target="_blank" rel="noreferrer noopener">seals</a>, penguins and whales over a six-year period,” noted study co-author Sebastian Menze, a scientist at the Norwegian Institute.



Such consistency implies the method can deliver rapid, reliable diagnostics as fishing tactics or quotas change.



“Consequently, our results show that acoustic data from fishing vessels and machine learning can act as a reliable foundation for rapid and convenient assessments of fisheries' interaction with the ecosystem,” Menze added.



Collecting those data costs almost nothing extra; crews already archive echo-sounder files as part of normal operations. The largest krill harvester, <a href="https://www.akerbiomarine.com/" target="_blank" rel="noreferrer noopener">Aker Biomarine</a>, even makes its records public through the <a href="https://www.hubocean.earth/platform" target="_blank" rel="noreferrer noopener">HUBOcean platform</a>.



<h2 class="wp-block-heading" id="h-positive-changes-in-krill-management">Positive changes in krill management </h2>



Until now, scientists mainly used fishery sonar to estimate krill biomass. The study’s broader ecological application opens fresh possibilities.



Bettina Meyer of AWI represents Germany on the <a href="https://www.ccamlr.org/en/organisation/home-page" target="_blank" rel="noreferrer noopener">Commission for the Conservation of Antarctic Marine Living Resources</a> (CCAMLR).



“We are expanding the potential uses for ecological questions and demonstrating new, cost-effective ways in which fishing vessels can contribute to krill fishery management,” said Meyer, who's also a senior author of the study. 



“Acoustic data make it possible to quickly draw an initial picture of how changes in fishery management or fleet behavior impact on the Antarctic ecosystem.”



Supported by Germany’s <a href="https://www.bmel.de/EN/Home/home_node.html" target="_blank" rel="noreferrer noopener">Federal Ministry of Food and Agriculture</a>, the project feeds directly into CCAMLR deliberations on updated catch limits and dynamic closure zones.



By revealing when and where krill fishing most conflicts with wildlife, the acoustic approach offers a blueprint for fine-tuned regulations. This could help ensure that the Southern Ocean’s keystone crustacean can sustain both its natural predators and the fishery that now depends on it.



The study is published in the journal <a href="https://www.pnas.org/doi/10.1073/pnas.2417203122" target="_blank" rel="noreferrer noopener">Proceedings of the National Academy of Sciences</a>.



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Sonar reveals how krill fishing is hurting Antarctic wildlife

Antarctic krill - the shrimp-like crustaceans that feed whales, seals,...

Rising nighttime temperatures could quietly aggravate one of the world’s most widespread sleep disorders: obstructive sleep apnea (OSA). This could bring steep costs to public health and the global economy.



This warning comes from a new study by sleep researchers at <a href="https://www.flinders.edu.au/" target="_blank" rel="noreferrer noopener">Flinders University</a>. The experts analyzed more than 58 million nights of sleep data and found a strong link between ambient temperature and breathing interruptions.



The results of the analysis suggest that, unless climate change is slowed, the worldwide burden of <a href="https://www.earth.com/news/obstructive-sleep-apnea-speeds-up-aging-on-a-cellular-level/" target="_blank" rel="noreferrer noopener">OSA</a> may double before today’s newborns reach old age.



<h2 class="wp-block-heading" id="h-a-billion-people-and-counting">A billion people and counting</h2>



OSA already affects nearly a billion adults. People with the disorder repeatedly stop breathing during sleep as throat tissues collapse. This leads to drops in blood oxygen, loud snoring, and dozens or even hundreds of brief awakenings each night.



Untreated OSA is tied to hypertension, <a href="https://www.earth.com/news/heart-disease-remains-the-leading-cause-of-death-worldwide/" target="_blank" rel="noreferrer noopener">heart disease</a>, cognitive decline, accidents, and depression. In Australia, the combined medical and productivity losses linked to poor sleep are estimated at roughly $66 billion per year.



Researchers knew little about how outdoor climate might influence the severity of the condition, despite its prevalence.



Bastien Lechat of the <a href="https://www.flinders.edu.au/fhmri/research/sleep-health" target="_blank" rel="noreferrer noopener">Flinders Health and Medical Research Institute (FHMRI) Sleep Health group</a> is lead author of the study.



“This helps us to understand how environmental factors like climate might affect health by investigating whether ambient temperatures influence the severity of OSA,” said Lechat.



<h2 class="wp-block-heading" id="h-linking-sleep-apnea-to-high-temperatures">Linking sleep apnea to high temperatures </h2>



Lechat’s team partnered with a digital health company that provides a thin, FDA-cleared sensor placed under the mattress. The device measures subtle pressure changes to track breathing and body movement.



The researchers collected an average of 500 consecutive nights of raw data for each of 116,000 anonymous users in 29 mainly high-income countries. Altogether, this added up to more than 30,000 user-years of continuous monitoring.



The team then merged those sensor records with hourly surface-air temperatures generated by high-resolution climate models.



By comparing night-to-night shifts in breathing disruptions with local temperature fluctuations, the team could isolate the effect of <a href="https://www.earth.com/news/extreme-heat-impacts-our-daily-routines-and-transportation/" target="_blank" rel="noreferrer noopener">heat</a> from other confounding factors such as age, weight, or chronic illness.



“Overall, we were surprised by the magnitude of the association between ambient temperature and OSA severity,” Lechat said. When the overnight temperature rose, apnea severity followed.



“Higher temperatures were associated with a 45 percent increased likelihood of a sleeper experiencing OSA on a given night.”



<h2 class="wp-block-heading" id="h-cooling-technology-may-buffer-heat-stress">Cooling technology may buffer heat stress</h2>



“These findings varied by region, with people in European countries seeing higher rates of OSA when temperatures rise than those in Australia and the United States, perhaps due to different rates of <a href="https://www.earth.com/news/ancient-buildings-used-passive-cooling-methods-to-reduce-heat-with-out-air-conditioning/" target="_blank" rel="noreferrer noopener">air conditioning</a> usage,” Lechat said.



In other words, cooling technology - and the affluence that underwrites it - can buffer heat-related sleep stress, while people in older buildings or lower-income areas remain vulnerable.


The researchers translated these nightly risks into long-term stakes by running a health-economics model. They based it on disability-adjusted life years (DALYs), the same yardstick the <a href="https://www.who.int/" target="_blank" rel="noreferrer noopener">World Health Organization</a> uses to compare illnesses.


“Using our modeling, we can estimate how burdensome the increase in OSA prevalence due to rising temperature is to society in terms of well-being and economic loss,” Lechat noted.



<h2 class="wp-block-heading" id="h-the-price-of-lost-sleep">The price of lost sleep</h2>



“The increase in OSA prevalence in 2023 due to global warming was associated with a loss of approximately 800,000 healthy life years across the 29 countries studied,” Lechat said.



“This number is similar to other medical conditions, such as bipolar disorder, <a href="https://www.earth.com/news/pesticide-exposure-increases-the-risk-of-parkinsons-disease/" target="_blank" rel="noreferrer noopener">Parkinson’s disease</a>, or chronic kidney diseases.”



The team also attached a price tag. “Similarly, the estimated total economic cost associated was $98 billion, including $68 billion from well-being loss and $30 billion from workplace productivity loss,” Lechat said.



Those figures reflect only the added harm from climate change, not the baseline burden of OSA from other causes. Looking ahead, the numbers get starker. 



According to Lechat, the findings highlight that without greater policy action to slow global warming, OSA burden may double by 2100 due to rising temperatures.”



<h2 class="wp-block-heading" id="h-sleep-study-misses-hot-regions">Sleep study misses hot regions</h2>



Senior author Danny Eckert, a sleep scientist at Flinders, points out important caveats. Wealthier nations and individuals who can afford a modern sleep tracker dominate the data set.



“This may have biased our estimates and led to an underestimation of the true health and economic cost,” he said.



Many of the hottest, least air-conditioned regions - South Asia, Africa, parts of Latin America - are underrepresented, yet stand to experience the strongest warming trends.



<h2 class="wp-block-heading" id="h-adapting-sleep-to-hotter-nights">Adapting sleep to hotter nights</h2>



Even as climate policy lags, the clinical community can act. “Higher rates of diagnosis and treatment will help us to manage and reduce the adverse health and productivity issues caused by climate-related OSA,” Eckert said.



Doctors still consider continuous positive airway pressure (CPAP) machines the gold-standard therapy. But alternative approaches - oral appliances, weight loss, and positional training - can also reduce breathing disturbances.



The next step for the researchers is to test protective strategies directly. “Going forward, we want to design intervention studies that explore strategies to reduce the impact of ambient temperatures on sleep apnea severity,” Eckert added.



For now, their message is clear: hotter nights are more than a comfort issue. They may be quietly robbing millions of restorative sleep, healthy years, and economic productivity - making <a href="https://www.earth.com/news/climate-mitigation-strategies-may-be-endangering-biodiversity/" target="_blank" rel="noreferrer noopener">climate mitigation</a>, bedroom cooling, and sleep-health screening part of the same urgent conversation.



The study is published in the journal <a href="https://www.nature.com/articles/s41467-025-60218-1" target="_blank" rel="noreferrer noopener">Nature Communications</a>.



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Rising temperatures are driving a surge in sleep apnea cases

Rising nighttime temperatures could quietly aggravate one of the world’s...

Ocean water is turning ever so slightly more acidic, and that small shift has now pushed the chemistry of the sea past a point that scientists once marked as the global “do not cross” line.



A new assessment shows that by 2020 the average concentration of calcium carbonate, a building block for shells and reefs, had fallen more than 20 percent from pre‑industrial levels in many regions. 



This results in a thinning of nature’s protective shield for corals, oysters, other mollusks, and countless plankton.



“<a href="https://www.earth.com/news/world-oceans-day-2025-sustaining-what-sustains-us/" target="_blank" rel="noreferrer noopener">Ocean</a> acidification isn’t just an environmental crisis, it’s a ticking timebomb for marine ecosystems and coastal economies,” said Professor Steve Widdicombe of Plymouth Marine Laboratory, after reviewing the study.



<h2 class="wp-block-heading" id="h-how-carbon-drives-ocean-acidity">How carbon drives ocean acidity</h2>



One extra molecule of carbon dioxide in the air means another will slip into the sea, combine with water, and release a hydrogen ion. 



Over the industrial era, that reaction has raised the average hydrogen ion concentration of the ocean about <a href="https://www.ipcc.ch/report/ar6/wg1/figures/chapter-5/figure-5-21/" target="_blank" rel="noreferrer noopener">30 percent</a> and knocked seawater pH down by roughly 0.1 units, which is a large jump on the logarithmic pH scale.



Many <a href="https://www.science.org/doi/abs/10.1126/science.1097329" target="_blank" rel="noreferrer noopener">calcifying </a>species depend on carbonate ions to form shells and skeletons; when ions grow scarce these organisms must divert energy from growth and reproduction toward basic survival. 



Laboratory work has shown that carbon‑rich water can dissolve the paper‑thin shells of the tiny sea butterfly <a href="https://hakaimagazine.com/news/the-shells-of-wild-sea-butterflies-are-already-dissolving/" target="_blank" rel="noreferrer noopener">Limacina helicina</a> within days.



<h2 class="wp-block-heading" id="h-ocean-acidity-crossed-the-safety-limit">Ocean acidity crossed the safety limit</h2>



The <a href="https://www.stockholmresilience.org/research/planetary-boundaries.html" target="_blank" rel="noreferrer noopener">planetary boundaries framework</a> was introduced to define the safe operating limits for Earth’s major life-supporting <a href="https://www.earth.com/news/ocean-climate-fixes-could-worsen-the-oxygen-crisis/" target="_blank" rel="noreferrer noopener">systems</a>. These boundaries act like guardrails; once crossed, the risk of large-scale environmental disruptions increases sharply. 



Out of nine total boundaries, including climate change and biodiversity loss, <a href="https://oceanservice.noaa.gov/facts/acidification.html" target="_blank" rel="noreferrer noopener">ocean acidification</a> was once thought to be safely within limits.



That assumption no longer holds. The latest study shows that the planet has already moved beyond the threshold meant to safeguard <a href="https://www.pmel.noaa.gov/co2/files/dickson_thecarbondioxidesysteminseawater_equilibriumchemistryandmeasurementspp17-40.pdf" target="_blank" rel="noreferrer noopener">marine carbonate chemistry</a>. What was once a buffer zone has become an active hazard. 



The proposed new limit is a 10 percent decline in carbonate levels from pre-industrial norms and that is now decades behind us.



<h2 class="wp-block-heading" id="h-ocean-acidity-now-affects-deep-waters">Ocean acidity now affects deep waters</h2>



The report, led by Dr. Helen Findlay and colleagues, stitched together 150 years of measurements and modeling to map acidity down to 660 feet (180 meters). 



Sixty percent of <a href="https://www.earth.com/news/darkening-oceans-are-shrinking-vital-marine-habitats/" target="_blank" rel="noreferrer noopener">waters</a> at that depth now sit beyond the old safety line, meaning the problem is not confined to sun‑lit shallows but reaches the heart of many food webs.



“Since these deeper waters are changing so much, the impacts of ocean acidification could be far worse than we thought,” noted Dr. Findlay, an ocean biogeochemist at <a href="https://pml.ac.uk/" target="_blank" rel="noreferrer noopener">Plymouth Marine Laboratory</a>.



<h2 class="wp-block-heading" id="h-reefs-and-jobs-are-at-risk">Reefs and jobs are at risk</h2>



Reefs cover <a href="https://oceanservice.noaa.gov/aa-updates/international-year-of-the-reef-022218.html" target="_blank" rel="noreferrer noopener">less than 1 percent</a> of the ocean floor yet shelter about a quarter of all marine species and buffer shorelines that more than 275 million people call home. 



The ongoing decline of coral reefs threatens food security, recreation, and an ocean tourism industry worth billions.



Shellfish growers have already felt the sting. Around 2010 hatcheries in the U.S. Pacific Northwest lost entire crops of oyster larvae when acidic upwelling water flooded their intake pipes, forcing emergency buffering and multi‑million‑dollar retrofits.



<h2 class="wp-block-heading" id="h-when-ocean-acidity-crossed-the-danger-line">When ocean acidity crossed the danger line</h2>



To confirm the timing of the threshold breach, the team combined surface records, ice‑core carbon dioxide data, and the <a href="https://oceanacidification.noaa.gov/ocean-acidification-data/" target="_blank" rel="noreferrer noopener">Global Ocean Acidification Observing Network</a>’s sensor archive. 



The models converged on the late 2010s as the moment the global average slipped past the 20 percent mark.



Importantly, that average hides stark regional contrasts. Polar seas, already low in carbonate, crossed the line earlier, while warm tropical basins hovered just above it until the past decade.



<h2 class="wp-block-heading" id="h-shrinking-safety-margin">Shrinking safety margin</h2>



The authors propose tightening the planetary boundary to a 10 percent decline, arguing that the original 20 percent buffer fails to protect deep <a href="https://www.earth.com/news/earths-oceans-are-rapidly-changing-colors-matching-climate-predictions/" target="_blank" rel="noreferrer noopener">reefs</a> and sensitive plankton. 



Under the looser standard, forty percent of the ocean surface is already in the danger zone; under the stricter one, almost the entire surface passed the limit by the early 2000s.



Moving the goalpost highlights how little headroom remains. Every additional ton of fossil‑fuel emissions steals more carbonate from seawater, and only aggressive cuts in carbon dioxide, along with emerging drawdown technologies, can reverse the chemical slide.



<h2 class="wp-block-heading" id="h-ocean-acidity-needs-more-than-local-fixes">Ocean acidity needs more than local fixes</h2>



Local fixes still matter. Seagrass beds that absorb CO₂, limits on coastal nutrient runoff, and refuges that protect genetic diversity can buy time for vulnerable species. 



However, Professor Widdicombe cautions that such measures “cannot solve acidification at the planetary scale.”



International agreements now recognize ocean acidification alongside warming, but policies lag behind science. 



The new findings give negotiators a clear metric - keep average carbonate depletion below 10 percent - to guide emission targets and monitor progress.



The study is published in the journal <a href="https://onlinelibrary.wiley.com/doi/10.1111/gcb.70238" target="_blank" rel="noreferrer noopener">Global Change Biology</a>.



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Ocean acidity crosses dangerous threshold, threatening marine life

Ocean water is turning ever so slightly more acidic, and...

Pangolins in Nigeria’s Cross River forests are in trouble. Most are killed for supper, not for overseas trade in their scales. A new field survey shows that nearly every pangolin taken from the wild ends up in a cooking pot.



Scientists from the <a href="https://www.cam.ac.uk/" target="_blank" rel="noreferrer noopener">University of Cambridge</a> spent three years talking with more than 800 hunters and traders across 33 villages. 



The team estimates that about 21,000 pangolins die each year in the region. Hunters rarely set out to look for them. They pick the animals up by hand while checking snares or working in farm plots. 



Almost three-quarters of the <a href="https://www.earth.com/news/the-meat-paradox-people-care-about-animals-but-still-eat-meat/" target="_blank" rel="noreferrer noopener">meat</a> is eaten by the hunters’ own families, and the rest is sold locally.



<h2 class="wp-block-heading" id="h-meat-is-the-motive-for-killing-pangolins">Meat is the motive for killing pangolins </h2>



Study lead author Dr. Charles Emogor conducted the research while pursuing his PhD in the Department of Zoology at Cambridge.



“Thousands of kilos of pangolin scales are seized at Nigeria’s ports, creating the impression that the international demand for scales is behind pangolin exploitation in West Africa,” said Dr. Emogor.



"When we spoke to hunters and traders on the ground around the Cross River forest, the largest stronghold for Nigeria’s pangolins, it was obvious that meat was the motivation for almost all of the pangolin killings.”



<h2 class="wp-block-heading" id="h-pangolin-scales-often-hit-the-bin">Pangolin scales often hit the bin</h2>



Less than a third of the scales from those animals ever reach a trader. Most are tossed aside. <a href="https://www.earth.com/news/does-hunting-fishing-connect-humans-with-nature-or-reinforce-superiority-complex/" target="_blank" rel="noreferrer noopener">Hunters</a> said meat earns three to four times more money per animal than scales do in local markets.



“We found that dedicated pangolin hunts are virtually non-existent. Most pangolins are killed by hunters out for any type of game,” said Dr. Emogor. 



"Around a third of pangolins are caught opportunistically, often while people are working in the fields. Pangolins curl into a ball when threatened, which sadly makes them easy to catch.”



<h2 class="wp-block-heading" id="h-a-prized-taste-and-old-beliefs">A prized taste and old beliefs</h2>



Pangolin meat is considered more flavorful than beef, chicken, or even antelope in many villages. It’s sometimes prepared for pregnant women, based on the belief that it promotes strong, healthy babies. 



This cultural value, combined with the species’ slow reproductive rate, puts intense <a href="https://www.earth.com/news/hundreds-of-mammals-show-how-humans-influence-animal-activity/" target="_blank" rel="noreferrer noopener">pressure</a> on the animal's survival.



“Pangolins face a lethal combination of threats,” said Dr. Emogor. “Pangolins are easy to hunt, breed slowly, taste good to humans, and are falsely believed to have curative properties in traditional medicines. In addition, their forest habitat is being destroyed.”



<h2 class="wp-block-heading" id="h-local-solutions-to-save-pangolins">Local solutions to save pangolins </h2>



Because food is the real pull, the researchers argue that local solutions - better patrols, new bylaws, and help with food security - may cost less and work faster than trying to police international trafficking alone.



“Clearly in designing any intervention we need good information on what’s motivating the hunters,” said study co-author Professor Andrew Balmford. “That’s why studies such as this are vital for effective conservation of endangered species.”



<h2 class="wp-block-heading" id="h-losing-80-million-years-of-evolution">Losing 80 million years of evolution</h2>



Dr. Emogor now runs Pangolino, a volunteer network that helps villages write and enforce pangolin-friendly rules. His motivation is personal as well as scientific.



"If we lose the pangolin, we lose 80 million years of evolution,” said Emogor. “Pangolins are the only mammals with scales, and their ancestors existed when dinosaurs still roamed the planet."



Cameroon, Gabon, and other nations show similar habits: people value pangolins mainly for food. Until diets change or enforcement improves, Africa’s only scaly <a href="https://www.earth.com/news/how-mammals-have-evolved-over-66-million-years/" target="_blank" rel="noreferrer noopener">mammals</a> will keep slipping toward extinction - one meal at a time.



<h2 class="wp-block-heading" id="h-protecting-pangolins-and-forest-life">Protecting pangolins and forest life</h2>



Efforts to save pangolins must go beyond curbing international trade. Protecting these animals - and the ecosystems they live in - means addressing the local drivers of hunting. 



That includes improving food security, offering economic alternatives to bushmeat, and increasing public awareness about the role pangolins play in forest health.



Education and outreach are key. Many hunters don’t realize pangolins are at risk. Some may not know the animals help control insect populations and support ecological balance. 



Wildlife conservation groups are working to spread this knowledge, while local governments and partners explore ways to boost law enforcement in remote areas.



Ultimately, protecting pangolins also helps safeguard other species that share their shrinking <a href="https://www.earth.com/news/north-americas-mammals-are-seeking-refuge-in-forest-habitats/" target="_blank" rel="noreferrer noopener">habitats</a>. When forests are preserved and hunting is managed sustainably, entire ecosystems stand a better chance of survival.



The full study was published in the journal <a href="https://www.nature.com/articles/s41559-025-02734-3" target="_blank" rel="noreferrer noopener">Nature Ecology &amp; Evolution</a>.



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Disturbing study finds the true reason this amazing creature is on the verge of extinction

Pangolins in Nigeria’s Cross River forests are in trouble. Most...

Scientists have puzzled over the brain’s memory storage system for decades. Many have wondered how our minds can file away new information without wiping out what we already know.



After rigorous investigations, researchers have found that <a href="https://www.sciencedirect.com/topics/neuroscience/place-cell" target="_blank" rel="noreferrer noopener">place cells</a> hold essential clues to this process. 



<a href="https://bcs.mit.edu/directory/ila-fiete">Ila Fiete</a>, a member of MIT’s <a href="https://mcgovern.mit.edu/" target="_blank" rel="noreferrer noopener">McGovern Institute for Brain Research</a> and the senior author of a recent study, believes these discoveries open fresh perspectives on how internal “maps” guide us to recall events with ease.



<h2 class="wp-block-heading" id="h-memory-storage-uses-scaffolding">Memory storage uses scaffolding</h2>



Place cells were first reported about half a century ago. Early <a href="https://pubmed.ncbi.nlm.nih.gov/5124915/" target="_blank" rel="noreferrer noopener">evidence</a> showed that they become active when a rodent occupies a particular spot in a maze. 



Further work revealed these cells reside in the <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC3548359/" target="_blank" rel="noreferrer noopener">hippocampus</a>, a core region for memory. They align with <a href="https://www.ncbi.nlm.nih.gov/books/NBK435751/" target="_blank" rel="noreferrer noopener">grid cells</a> in the entorhinal cortex.



Together, these populations form a foundation. Both spatial details and personal experiences rest on this scaffold, ensuring that details remain anchored to distinct neural patterns.



The recent model, called vector hippocampal scaffolded heteroassociative memory <a href="https://pubmed.ncbi.nlm.nih.gov/39814883/" target="_blank" rel="noreferrer noopener">(Vector-HaSH)</a>, proposes that the hippocampus functions a bit like an index. 



It holds pointers, which direct the brain to the finer content stored in vast areas of <a href="https://www.sciencedirect.com/topics/medicine-and-dentistry/sensory-cortex" target="_blank" rel="noreferrer noopener">sensory cortex</a>. That index can then “fill in” previously stored information whenever we recall it.



“This model is a first-draft model of the <a href="https://www.frontiersin.org/journals/human-neuroscience/articles/10.3389/fnhum.2024.1448791/full" target="_blank" rel="noreferrer noopener">entorhinal-hippocampal</a> episodic memory circuit. That’s the thing I’m really excited about,” said Fiete.



In simpler words, the hippocampus does not permanently hold every detail. It directs us to the right place in the cortex, where the nuts and bolts of each stored memory lie.



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



The hippocampus is tucked deep within the medial temporal lobe. Because of it's crucial role in converting short-term memories into long-term ones, without <a href="https://www.earth.com/news/sleep-reboots-the-brain-making-room-for-new-memories/" target="_blank" rel="noreferrer noopener">the hippocampus</a>, experiences would simply fade away moments after they occurred. 



This brain region also helps us navigate space, build mental maps, and orient ourselves in our environments.



It works closely with the amygdala and <a href="https://www.earth.com/news/new-brain-pathways-identified-as-being-unique-to-humans/" target="_blank" rel="noreferrer noopener">prefrontal cortex</a>, forming a network that governs how we learn from experience and respond emotionally to events.



Damage to the hippocampus can lead to serious memory issues, such as anterograde amnesia - the inability to form new memories. 



This kind of impairment has been observed in patients with Alzheimer’s disease and in cases of brain trauma or stroke. 



Research also shows that the hippocampus is highly plastic - it can grow new neurons even in adulthood, a process known as neurogenesis.



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



Grid cells create repeated patterns that look like triangular lattices. Each triangular arrangement, referred to as a well, can point to a specific episode. 



The content itself is not housed in these wells. Instead, each well is a label that refers the <a href="https://www.earth.com/news/17-best-strategies-to-protect-your-brain-from-stroke-dementia-and-depression/" target="_blank" rel="noreferrer noopener">brain</a> to the correct memory storage location in the sensory cortex.



As more events pour in, the circuit spreads them out, allowing older memories to fade gently. The model bypasses the so-called memory cliff, a snag that often affects older computational frameworks. 



This design reflects how real neural networks accommodate both new items and older recollections without hitting a harsh limit.



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



Training for events that require memorizing large sets of information can benefit from these findings. The time-honored <a href="https://www.nature.com/articles/nn988" target="_blank" rel="noreferrer noopener">memory palace method</a> aligns with the notion of using spatial backdrops to link to new data.&nbsp;



Experts often picture a familiar location and place items there in a structured sequence. Later, they mentally revisit each spot to retrieve those items. 



This new model suggests that tapping an already entrenched memory storage map can free up cognitive space for large-scale memorization.



The principle is straightforward. By designating specific neural wells as placeholders, we can link a chain of events without jumbling them up. 



Our internal index system calls up the correct cluster of cells. That cluster cues the finer content that is stashed in sensory regions.



<h2 class="wp-block-heading" id="h-sequential-order-explained">Sequential order explained</h2>



Sometimes, we need to <a href="https://www.earth.com/news/sleep-rewires-the-brain-to-strengthen-memories/" target="_blank" rel="noreferrer noopener">recall</a> a story in the exact order it happened. This framework highlights that each well holds cues about what comes next. 



That helps us replay those experiences in the correct sequence. The model draws on the same arrangement for both location-based and experience-based details.



Memories about where you ate lunch last week or how you maneuvered a tricky hiking trail can emerge from the same scaffolding. You tap the index that leads you to the right well, and the rest naturally falls into place.



<h2 class="wp-block-heading" id="h-future-memory-storage-studies">Future memory storage studies</h2>



One area of interest is how short-term recollections solidify into more general facts. These are sometimes called semantic memories. 



The fresh approach provides a structure for investigating how personal events might become separated from contextual details after enough time.



Researchers also want to clarify how episodes are chunked or defined. 



Another question is whether a model like Vector-HaSH can fuel more efficient machine <a href="https://www.earth.com/news/scientists-discover-a-better-way-for-kids-to-learn-math/" target="_blank" rel="noreferrer noopener">learning</a>. Understanding how the brain organizes sequences might help AI systems handle incremental learning.



This study supports the idea that hippocampal and entorhinal circuits form an integrated reference system for storing huge amounts of information without abrupt loss.



All of this underscores that the same circuit that once guided our ancestors through forests and deserts can also manage recollections of birthdays, daily errands, and major life milestones.



The study is published in <a href="https://www.nature.com/articles/s41586-024-08392-y" target="_blank" rel="noreferrer noopener">Nature</a>.



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Human brains use a storage trick to keep your memories in sequential order

Scientists have puzzled over the brain’s memory storage system for...

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...

Most insects, including many beetles, cannot see red. Their eyes detect ultraviolet, blue, and green light. Bees often visit red flowers, but not for their color. They are drawn to ultraviolet reflections, not the red hue itself.



But two Mediterranean beetles break that pattern.&nbsp;Pygopleurus chrysonotus&nbsp;and&nbsp;Pygopleurus syriacus&nbsp;can truly perceive red. They seek out red flowers, especially poppies, anemones, and buttercups, for pollen. Their eyes are uniquely tuned to do this.



<h2 class="wp-block-heading" id="h-beetles-with-a-four-color-vision-system">Beetles with a four-color vision system</h2>



‘To our knowledge, we are the first to have experimentally demonstrated that <a href="https://www.earth.com/news/insects-are-still-disappearing-and-there-are-hundreds-of-reasons-why/" target="_blank" rel="noreferrer noopener">beetles</a> can actually perceive the color red,’ said Dr Johannes Spaethe.



The researchers confirmed this by recording electrical activity from photoreceptors in beetle eyes. They discovered four photoreceptor types. These respond to ultraviolet, blue, green, and red wavelengths.



This tetrachromatic system is rare among beetles. Most have just two or three receptor types. Blue sensitivity, previously missing in some beetle lineages, reappears here. It likely evolved through a gene duplication event and a spectral shift from ultraviolet.



<h2 class="wp-block-heading" id="h-beetles-choose-red-over-grey">Beetles choose red over grey</h2>



Photoreceptors are light-sensitive cells in the eye. Just having them doesn't prove an animal can&nbsp;see&nbsp;colors. To show true color vision, an animal must tell colors apart even when they have the same brightness.



To test this, scientists used a trick from bee research by Von Frisch. They gave beetles a choice between red circles and grey ones that varied in brightness. If beetles picked red over all shades of grey, it meant they could see red as a distinct color - not just as a lighter or darker patch.



That’s exactly what happened. In every test, beetles chose red first. The researchers also ran a second test in the wild using traps in five colors. Almost all P. chrysonotus beetles ended up in red traps. This showed their natural color preference matched the lab findings.



<h2 class="wp-block-heading" id="h-opponency-and-complex-visual-processing">Opponency and complex visual processing</h2>



Recordings also revealed opponency signals. These occur when one receptor type’s signal suppresses another. It is a marker of complex color processing. 



For example, red receptors showed suppressed responses in green wavelengths. This confirmed interaction between channels.



This kind of opponency, previously seen in <a href="https://www.earth.com/news/modern-farming-is-causing-many-insect-species-to-collapse/" target="_blank" rel="noreferrer noopener">butterflies</a>, suggests advanced neural processing. It likely helps the beetles make sharp color distinctions in complex natural environments.



<h2 class="wp-block-heading" id="h-evolution-of-beetles-and-red-flowers">Evolution of beetles and red flowers </h2>



Why do these <a href="https://www.earth.com/news/very-little-is-known-about-99-of-all-insects-on-earth/" target="_blank" rel="noreferrer noopener">beetles</a> care so much about red? It may reflect a mutual evolutionary pathway. Red flowers in the Mediterranean are mostly pollinated by Glaphyridae beetles. These flowers form the “poppy guild.”



‘The prevailing opinion in science is that flower colours have adapted to the visual systems of pollinators over the course of evolution,’ says Spaethe.



Yet this case flips that assumption. Glaphyrid beetles may have evolved their vision to match flower color diversity. 



Within their family, different genera prefer different flower colors such as yellow, white, violet, and red. This suggests their visual systems may be flexible and evolving alongside flowers.



<h2 class="wp-block-heading" id="h-red-vision-helps-beetles-access-flowers">Red vision helps beetles access flowers</h2>



Specializing in red gives beetles an advantage. Most insects cannot see red. That means red flowers are invisible or less noticeable to them.



But&nbsp;P. chrysonotus&nbsp;and&nbsp;P. syriacus&nbsp;can see red clearly. This gives them special access to food - like pollen - from red flowers that others ignore.



Because fewer insects compete for red flowers, the beetles face less crowding. They also become more reliable pollinators for those flowers.



Over time, flowers may evolve to become red on purpose. This helps attract only beetles and avoid unwanted visitors like bees that may steal pollen without pollinating. This is what scientists call a "private niche in color space."



<h2 class="wp-block-heading" id="h-rare-window-into-insect-vision">Rare window into insect vision</h2>



P. chrysonotus&nbsp;and&nbsp;P. syriacus&nbsp;are now among the few <a href="https://www.earth.com/news/rising-heat-shrinking-habitats-insects-face-hidden-threats/" target="_blank" rel="noreferrer noopener">insects</a> with confirmed red color vision. Their unique tetrachromatic eyes, behavioral responses, and flower preferences paint a new picture of insect-flower interaction.



This research does more than reveal a rare trait. It creates a valuable model for studying pollination, vision, and co-evolution, all through the eyes of beetles.



The study is published in the <a href="https://journals.biologists.com/jeb/article/doi/10.1242/jeb.250181/368218/Remarkable-red-colour-vision-in-two-Mediterranean" target="_blank" rel="noreferrer noopener">Journal of Experimental Biology</a>. 



Image Credit: Johannes Spaethe / University of Würzburg



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Beetles that see red break the rules of insect vision

Most insects, including many beetles, cannot see red. Their eyes...

Axolotls have charmed the world with their feathery gills and perpetual smiles. However, their true superpower lies in their ability to regrow lost limbs - even hands, arms, and parts of organs - without leaving a single scar.



This rare ability sets axolotls apart from almost all other vertebrates. Scientists have long looked to them as a living model for unlocking the secrets of <a href="https://www.earth.com/news/axolotls-regeneration-powers-critically-endangered/" target="_blank" rel="noreferrer noopener">regeneration</a>.



<h2 class="wp-block-heading" id="h-secrets-of-axolotl-healing">Secrets of axolotl healing</h2>



In a study led by <a href="https://www.northeastern.edu/" target="_blank" rel="noreferrer noopener">Northeastern University</a> biologist James Monaghan, researchers asked a question that has puzzled scientists for almost two centuries: How does an axolotl know which body part to rebuild and how much of it to replace?



“It could help with scar-free wound <a href="https://www.earth.com/news/secrets-of-killifish-regeneration-may-help-us-heal-humans/" target="_blank" rel="noreferrer noopener">healing</a> but also something even more ambitious, like growing back an entire finger,” said Monaghan. “It’s not out of the realm of possibility to think that something larger could grow back like a hand.”



Monaghan traced the animal’s “positional memory” to a common signaling molecule called retinoic acid. Inside the axolotl’s arm, retinoic acid forms a gradient - high near the shoulder, low near the fingertips. Fibroblast cells read that gradient like a map and decide what to build.



“The cells can interpret this cue to say, ‘I’m at the elbow, and then I’m going to grow back the hand’ or ‘I’m at the shoulder. I have high levels of retinoic acid, so I’m going to then enable those cells to grow back the entire limb,’” noted Monaghan.



<h2 class="wp-block-heading" id="h-rewriting-the-regeneration-plan">Rewriting the regeneration plan</h2>



To test the system, the team boosted retinoic-acid levels in a <a href="https://www.earth.com/news/skydiving-salamanders-can-fully-control-blood-flow-in-their-toes/" target="_blank" rel="noreferrer noopener">salamander</a>’s hand. The result was startling: instead of one new hand, the axolotl sprouted a duplicate limb.



Monaghan said the experiment was "pretty Frankensteiny." Still, it showed that tweaking the signal can rewrite the regeneration plan.



People make retinoic acid too, and our fibroblasts help mend <a href="https://www.earth.com/news/healing-chronic-wounds-with-gold-and-red-wine/" target="_blank" rel="noreferrer noopener">wounds</a>. The problem is that human cells ignore the signals that axolotls obey. They lay down collagen and form scars instead of new tissue.



“If we can find ways of making our fibroblasts listen to these regenerative cues, then they’ll do the rest,” said Monaghan. “They know how to make a <a href="https://www.earth.com/news/limb-development-genes-connected-to-fingerprints/" target="_blank" rel="noreferrer noopener">limb</a> already because, just like the salamander, they made it during development.”



<h2 class="wp-block-heading" id="h-the-genetics-of-axolotl-healing">The genetics of axolotl healing</h2>



Digging deeper, the researchers linked retinoic-acid signaling to the short homeobox gene (shox). 



When they removed shox with CRISPR-Cas9, the salamanders grew stubby arms capped by normal-size hands - the same limb pattern seen in people who carry a SHOX mutation.



“In order for regenerative biology or regenerative medicine to move forward, we need to understand where positional memory lies and how to manipulate it and engineer it,” explained Monaghan. 



“How do you make a cell move where you want? Changing its positional memory is critical for this.”



<h2 class="wp-block-heading" id="h-searching-for-the-healing-control-switch">Searching for the healing control switch </h2>



Monaghan’s lab is now probing the inner workings of fibroblasts to find out exactly how retinoic acid flips genetic switches like shox. 



Cracking that code could bring medicine a step closer to scar-free <a href="https://www.earth.com/news/blueberries-could-be-key-to-treating-non-healing-wounds/" target="_blank" rel="noreferrer noopener">healing</a> - and, one day, the chance to replace more than a fingertip.



For now, the smiling axolotl keeps teaching us that the blueprints for regeneration are already inside our own cells. The challenge is learning how to read them.



<h2 class="wp-block-heading">What this could mean for medicine</h2>



While limb regrowth in humans may still sound like science fiction, scientists see realistic opportunities for smaller steps in the near future. 



Advances in regenerative cues and gene targeting could lead to new ways to treat severe injuries, reduce scarring after surgery, or even regrow damaged cartilage.



Rather than trying to grow an entire arm right away, researchers envision using the axolotl’s secrets to guide healing in stages - like rebuilding bone, restoring tissue layers, or regenerating nerves. 



Understanding how fibroblasts respond to positional signals may also open new paths for treating birth defects or degenerative diseases.



The full study was published in the journal <a href="https://www.nature.com/articles/s41467-025-59497-5" target="_blank" rel="noreferrer noopener">Nature Communications</a>.



Image Credit: Alyssa Stone/Northeastern University



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Secrets of axolotl healing could teach us how to regrow limbs

Axolotls have charmed the world with their feathery gills and...

Human evolution is not only about bones. It is about the forests, soils, and climates that supported early apes long before the first hominin walked upright. 



Though great apes diverged from other primates around 25 million years ago, our own lineage did not appear until roughly 5 million years ago. In that immense stretch of time, forests rose and fell, volcanoes erupted, and ancient <a href="https://www.earth.com/news/earth-day-2025-our-power-our-planet/" target="_blank" rel="noreferrer noopener">creatures</a> adapted to the world around them.



One place where this deep story unfolds is western Kenya’s Koru 16. This fossil site captures a snapshot of life during the early Miocene, around 20 million years ago. Preserved by ash from the long extinct Tinderet Volcano, Koru 16 is a rich and complex time capsule. 



New research led by Venanzio Munyaka reveals that the story of ape evolution cannot be told without understanding the ecosystems they called home. The study adds fresh insight to a region already steeped in fossil history.



<h2 class="wp-block-heading" id="h-ape-fossils-reveal-evolutionary-activity">Ape fossils reveal evolutionary activity</h2>



Koru 16 has drawn scientific interest for nearly a hundred years. The site’s first primate fossils were discovered in 1927, and legendary anthropologist Louis Leakey led several excavations in the decades that followed. 



While those early efforts laid important groundwork, the last decade brought new urgency and better tools for understanding its full ecological <a href="https://www.earth.com/news/apes-can-tell-when-humans-dont-know-something/" target="_blank" rel="noreferrer noopener">context</a>.



Between 2013 and 2023, Munyaka and colleagues carried out a detailed investigation at two subsites. They recovered nearly 1,000 fossil leaves and a wealth of vertebrate remains. 



The bones came from 25 different species, including pythons, rodents, and three types of apes. These included Proconsul africanus, Proconsul major, and a newly identified large bodied nyanzapithecine.



These discoveries make Koru 16 the most ape rich site within the wider Tinderet group. The presence of multiple ape species in a single forested environment suggests the region played a key role in early ape evolution. But it was not just the bones that told a story.



<h2 class="wp-block-heading" id="h-changing-forests-shaped-how-early-apes-lived">Changing forests shaped how early apes lived</h2>



The team used a combination of paleosol chemistry, leaf structure, and tree stump fossils to reconstruct what Koru 16 looked like millions of years ago. Their results point to a warm, wet tropical forest, interrupted frequently by natural disturbances. 



Volcanic eruptions from the Tinderet complex blanketed the land with ash. Wildfires and seasonal floods added further stress.



Yet through all this, life thrived. Soil analyses indicate the region received about 2,000 mm of rainfall per year, with temperatures likely above 25°C. These conditions are similar to modern tropical forests in Africa, though the vegetation was slightly different. Koru 16’s forest likely had more deciduous trees, with plants that dropped their leaves seasonally.



“By studying the soil, fossils, and tree stumps, we could recreate the forest's climate,” said Munyaka. The climate was not stable. Instead, it was a shifting mosaic of dense forest, open patches, and recently disturbed areas. This landscape would challenge and shape the <a href="https://www.earth.com/news/what-animal-will-replace-humans-as-earths-dominant-species-this-scientist-has-an-idea/" target="_blank" rel="noreferrer noopener">creatures</a> living there.



<h2 class="wp-block-heading" id="h-leaves-light-and-forest-layers">Leaves, light, and forest layers</h2>



Plant fossils offered a vivid picture of this forest. From the two subsites, researchers cataloged 18 distinct leaf morphotypes. These belonged to plants that likely had short lifespans and fast growth cycles. 



Such traits suggest a forest marked by high turnover, where plants quickly colonized open areas after fires or ashfalls.



Most of the fossilized leaves came from <a href="https://www.earth.com/news/earth-day-2025-innovation-takes-the-lead-in-environmental-action/" target="_blank" rel="noreferrer noopener">species</a> adapted to both shaded understories and sunlit clearings. This indicates a mixed canopy, with parts of the forest densely shaded and others exposed. The forest structure would have influenced how apes moved, fed, and nested. 



Some leaves had characteristics similar to those found in modern forests in Uganda and Madagascar, places where rainfall is seasonal and disturbance is common.



The researchers also found casts of fossilized tree stumps. In one subsite, stumps stood close together, suggesting a mature, shaded forest. In the other, stumps were widely spaced, hinting at a more open, disturbed area. 



These contrasts imply that even within a small region, early Miocene forests were ecologically diverse and constantly in flux.



<h2 class="wp-block-heading" id="h-apes-among-the-ash">Apes among the ash</h2>



The fauna found alongside the plants reinforce this view. Apes were not alone. The site also yielded fossils of large pythons and several rodent species. The dominance of rodents reflects a rich, layered ecosystem. 



Most importantly, the three ape species discovered show that such forests supported a range of primate forms, including some of our most ancient relatives.



“The forest was not a quiet, uniform place,” said one researcher. “It was full of challenges that spurred change.” These challenges likely encouraged the development of new behaviors. Apes may have moved more on the ground, adapted their diets to seasonal food, or evolved new social habits to cope with ecological instability.



This type of environment, warm, seasonal, and disturbed, would have offered opportunities and obstacles. Forest fragmentation and frequent change may have nudged primates toward flexibility in how they lived, moved, and survived. In that sense, the forest itself became an evolutionary partner.



<h2 class="wp-block-heading" id="h-ecological-roots-of-evolution">Ecological roots of evolution</h2>



Koru 16 forces a shift in how we think about ape origins. Rather than emerging in calm, unchanging rainforests, early apes lived in dynamic, fractured landscapes. 



These habitats were shaped by fire, flood, and ash. The soil, climate, and plants constantly shifted, creating a stage that demanded adaptability.



The presence of multiple ape species in this kind of forest suggests that environmental variability did not limit primate evolution. It may have energized it. The ability to navigate change, rather than thrive in stability, might have been a key evolutionary trait.



Through its ancient layers of ash and soil, Koru 16 gives us something rare. It offers a full picture of the world early apes inhabited. It tells a story not just of bones, but of climate, ecology, and survival. 



The research reminds us that the journey to becoming human began not just in upright steps but in leafy canopies, open glades, and the fertile ash beds of a forest always on the move.



The study is published in the journal <a href="https://agupubs.onlinelibrary.wiley.com/doi/10.1029/2025PA005152" target="_blank" rel="noreferrer noopener">Paleoceanography and Paleoclimatology</a>.



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Early apes lived in a constantly changing world of fire and ash

Human evolution is not only about bones. It is about...

Dinosaurs have long captivated human imagination. From towering giants to quick-footed hunters, these creatures ruled the prehistoric world for millions of years. Each fossil discovery brings new understanding. 



A recent find has added a key piece to the tyrannosaur story. Named Khankhuuluu mongoliensis, this newly identified dinosaur sheds light on how smaller predators evolved into giants like Tyrannosaurus rex.



This breakthrough comes from a global research team led by Jared Voris and Dr. Darla Zelenitsky of the <a href="https://ucalgary.ca" target="_blank" rel="noreferrer noopener">University of Calgary</a>. Their findings appear in the journal Nature. 



Khankhuuluu lived about 86 million years ago during a time of rapid change.



As other large <a href="https://www.earth.com/news/fossilized-guts-reveal-the-eating-habits-of-sauropod-dinosaurs/" target="_blank" rel="noreferrer noopener">predators</a> vanished, new ones took their places. Khankhuuluu stood at the crossroads of this transition. The species bridges the gap between earlier swift hunters and the colossal bone crushers that followed.



<h2 class="wp-block-heading" id="h-khankhuuluu-came-before-t-rex">Khankhuuluu came before T. rex</h2>



Khankhuuluu means “prince of dragons” in Mongolian. The name hints at its importance. It was not yet king, but it was certainly part of a royal bloodline.



This dinosaur is now seen as the closest-known ancestor of the tyrannosaurs. Unlike its massive descendants, Khankhuuluu weighed only about 750 kilograms (1,600 pounds). That is similar to the size of a modern horse.



“This new species provides us the window into the ascent stage of tyrannosaur evolution; right when they’re transitioning from small predators to their apex <a href="https://www.earth.com/news/dinosaur-fossils-reveal-cancer-clues-for-modern-medicine/" target="_blank" rel="noreferrer noopener">predator</a> form,” explained Jared Voris, the study’s first author and a Ph.D. candidate at the University of Calgary.



Khankhuuluu rose to prominence after the extinction of many other large carnivores. It seized the opportunity and evolved new traits that would eventually lead to its dominance.



<h2 class="wp-block-heading" id="h-fast-agile-and-built-to-pursue">Fast, agile, and built to pursue</h2>



Khankhuuluu was not a brute force <a href="https://www.earth.com/news/ancient-footprints-reveal-a-dinosaur-that-changed-pace-while-walking/" target="_blank" rel="noreferrer noopener">predator</a>. It had a long, shallow skull that lacked the bone-crushing strength of a T. rex. Instead, it relied on its long legs for speed, and its sharp senses. Scientists describe it as a mesopredator, similar in role to a coyote. 



This means it likely preyed on small animals and used agility to avoid larger threats.



One of its most notable features was a pair of tiny horns above its eyes. These were likely used for mating displays or to intimidate other dinosaurs.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/06/dinosaur_t-rex-cousin_Khankhuuluu-mongoliensis_credit-UCalgary_1m.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/06/dinosaur_t-rex-cousin_Khankhuuluu-mongoliensis_credit-UCalgary_1s.webp" alt="This artist's illustration shows the newly discovered dinosaur species Khankhuuluu mongoliensis, an ancestor of Tyrannosaurus Rex. Misidentified bones actually belong to a new species of tyrannosaur which rewrites the family history of the mighty T-Rex. Credit: University of Calgary" class="wp-image-1973997"/></a><figcaption class="wp-element-caption">This artist's illustration shows the newly discovered dinosaur species Khankhuuluu mongoliensis, an ancestor of Tyrannosaurus Rex. Misidentified bones actually belong to a new species of tyrannosaur which rewrites the family history of the mighty T-Rex. Click image to enlarge. Credit: University of Calgary</figcaption></figure>



Later species such as Albertosaurus and Gorgosaurus would develop larger and more ornate versions of these horns. 



In Khankhuuluu, however, the structures were still in early development. These subtle differences mark it as a transitional figure in tyrannosaur history.



<h2 class="wp-block-heading" id="h-khankhuuluu-was-misidentified">Khankhuuluu was misidentified</h2>



The bones that identified Khankhuuluu were not newly dug from the ground. They were actually collected in the 1970s by paleontologist Altangerel Perle in the Bayanshiree Formation in southeastern Mongolia. 



At the time, the fossils were thought to belong to a dinosaur called Alectrosaurus that was more commonly found in nearby China. That assumption held for decades.



Then in 2023, Voris traveled to Mongolia to study the fossils in detail. While examining the material at the Institute of Paleontology, he noticed key differences. These included unique features in the skull and limbs. 



These observations confirmed that the fossils belonged to a new <a href="https://www.earth.com/news/archaeopteryx-fossil-soft-tissue-flight-evolution-proves-darwin-right/" target="_blank" rel="noreferrer noopener">species</a>. What had once been misidentified was now recognized as a pivotal ancestor of the tyrannosaurs.



<h2 class="wp-block-heading" id="h-the-tyrannosaur-that-crossed-continents">The tyrannosaur that crossed continents</h2>



Khankhuuluu's legacy is not limited to Mongolia. Its lineage spread far beyond Asia. 



“Khankhuuluu, or a closely related species, would have immigrated to North America from Asia around 85 million years ago. Our study provides solid evidence that large tyrannosaurs first evolved in North America as a result of this immigration event,” Dr. Darla Zelenitsky noted.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/06/dinosaur_t-rex-cousin_Khankhuuluu-mongoliensis_paleontologists_credit-UCalgary_1big.jpg" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/06/dinosaur_t-rex-cousin_Khankhuuluu-mongoliensis_paleontologists_credit-UCalgary_1s.webp" alt="Darla Zelenitsky, a paleontologist and associate professor in the Faculty of Science, and Jared Voris, a Ph.D. candidate, have identified a new species of dinosaur named Khankhuuluu. They, along with a team of international scientists, have published a paper in the journal, Nature, about the evolution of Tyrannosaurs. Credit: Riley Brandt/University of Calgary" class="wp-image-1974000"/></a><figcaption class="wp-element-caption">Darla Zelenitsky, a paleontologist and associate professor in the Faculty of Science, and Jared Voris, a Ph.D. candidate, have identified a new species of dinosaur named Khankhuuluu. They, along with a team of international scientists, have published a paper in the journal, Nature, about the evolution of Tyrannosaurs. Click image to enlarge. Credit: Riley Brandt/University of Calgary</figcaption></figure>



This migration shaped the history of dinosaurs on both continents. Once in North America, tyrannosaurs began to grow larger and more specialized. Over time, they became the most dominant predators in their environments. 



The journey of Khankhuuluu set this in motion. It is a clear example of how species movement influences evolution.



<h2 class="wp-block-heading" id="h-how-tyrannosaurs-split">How tyrannosaurs split</h2>



Once in North America, the tyrannosaurs evolved along two main paths. One group became massive apex predators like Tyrannosaurus rex. 



These were the bone crushers, armed with powerful jaws and deep skulls. Another group developed long snouts and stayed medium-sized. Scientists call them “Pinocchio rexes” because of their distinctive faces.



Both branches trace back to Khankhuuluu or a very similar <a href="https://www.earth.com/news/dinosaur-extinction-theories-are-challenged-by-new-research/" target="_blank" rel="noreferrer noopener">ancestor</a>. This new discovery shows that the migration from Asia was not just a one-time event. It reveals a pattern of interaction and development that shaped dinosaur evolution.



These findings change the way scientists view the rise of tyrannosaurs. The journey was not linear. It involved branching, mixing, and adapting over millions of years.



<h2 class="wp-block-heading" id="h-next-chapter-in-the-tyrannosaur-story">Next chapter in the tyrannosaur story</h2>



Though Khankhuuluu has answered many questions, it has also raised new ones. Researchers now want to explore earlier stages of tyrannosaur evolution. 



What came before the dragon prince? What traits defined the first members of this mighty family? The answers may lie buried in rocks still waiting to be exposed.



For now, Khankhuuluu stands as a symbol of change. It was not the biggest or most fearsome predator. But it played a critical role in the story of Earth's past. 



As the dragon prince, it holds the key to understanding how some of the most iconic creatures in history came to rule the land.



The study is published in the journal <a href="https://www.nature.com/articles/s41586-025-08964-6" target="_blank" rel="noreferrer noopener">Nature</a>.



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Meet the "prince of dragons," closest T-rex relative that started the tyrannosaur dynasty

Dinosaurs have long captivated human imagination. From towering giants to...

Two small cubs that died more than 14,000 years ago, were initially considered to be early domesticated dogs. New findings now confirm that these so-called "puppies" were actually wolf cubs. Their final nap, curled up in their den, turned them into scientific time capsules.



Their frozen remains - discovered in northern Siberia - were so well preserved that researchers could study what they ate, how they lived, and how they died.



<h2 class="wp-block-heading" id="h-where-the-wolf-cubs-were-found">Where the wolf cubs were found</h2>



The cubs were found about 40 kilometers (25 miles) from the village of Tumat in Siberia. One was unearthed in 2011 and the other in 2015, at what is now known as the Syalakh site.



Both were buried deep within frozen soil layers, preserved by permafrost alongside <a href="https://www.earth.com/news/woolly-mammoth-fossil-freeze-dried-skin-active-dna-chromosomes-52000-years/" target="_blank" rel="noreferrer noopener">mammoth</a> bones that showed signs of having been burned and butchered.



This unusual combination of human activity and frozen remains sparked early speculation. Some believed the cubs might have been <a href="https://www.earth.com/news/from-wolves-to-dogs-did-domestication-begin-without-human-help/" target="_blank" rel="noreferrer noopener">early dogs</a>, living among humans or scavenging near human settlements. 



The fact that their fur was black - a trait once thought to be unique to domesticated dogs - added fuel to the theory.



<h2 class="wp-block-heading" id="h-university-of-york-sheds-new-light">University of York sheds new light</h2>



But new research from the <a href="https://www.york.ac.uk/" target="_blank" rel="noreferrer noopener">University of York</a> tells a different story. Scientists studied genetic material from the cubs’ stomachs, along with chemical signals in their bones, teeth, and tissue. 



The data pointed not to early dogs, but to wolves - wolves that had lived wild and free during the <a href="https://www.earth.com/news/humans-were-likely-the-leading-cause-of-megafauna-extinctions/" target="_blank" rel="noreferrer noopener">Pleistocene</a>.



The cubs were about two months old and still nursing. But they were also eating solid food, including meat from a wooly rhinoceros and, in one case, a small bird called a wagtail. 



The presence of undigested rhino skin in one cub’s stomach points to how recently they had eaten, and how abruptly their lives had ended.



“It was incredible to find two sisters from this era so well preserved, but even more incredible that we can now tell so much of their story, down to the last meal that they ate,” said Anne Kathrine Runge from the University of York’s Department of Archaeology.



<h2 class="wp-block-heading" id="h-sister-wolf-cubs-lost-in-a-collapse">Sister wolf cubs lost in a collapse</h2>



The cubs showed no signs of injury or attack. Researchers believe they were resting in their den, possibly after feeding, when a landslide or collapse trapped them. 



“Whilst many will be disappointed that these animals are almost certainly wolves and not early domesticated dogs, they have helped us get closer to understanding the environment at the time, how these animals lived, and how remarkably similar wolves from more than 14,000 years ago are to modern day wolves," explained Runge.



"It also means that the mystery of how dogs evolved into the domestic pet we know today deepens, as one of our clues - the black fur color - may have been a red herring given its presence in wolf cubs from a population that is not related to domestic dogs,” she added.



<h2 class="wp-block-heading" id="h-life-in-a-rich-landscape">Life in a rich landscape</h2>



Inside the wolf cubs’ stomachs were fossilized remains of plants such as prairie grasses, willow twigs, and leaves from Dryas shrubs. This suggests they lived in a varied and rich ecosystem, full of edible plants and animals.



Despite their proximity to mammoth bones, there was no sign that the cubs ate mammoth meat. Instead, researchers found clear evidence of <a href="https://www.earth.com/news/humans-hunted-woolly-rhinoceros-to-extinction/" target="_blank" rel="noreferrer noopener">wooly rhinoceros</a> in their diet.



Although a fully grown rhino would be far too large for a cub - or even a single adult wolf - to bring down, scientists think the prey was likely a young calf taken down by the pack and shared with the cubs.



<h2 class="wp-block-heading" id="h-bigger-wolves-bigger-prey">Bigger wolves, bigger prey?</h2>



The idea of wolves hunting wooly rhinos, even young ones, has raised questions. Could these ancient wolves have been larger and more powerful than today’s <a href="https://www.earth.com/news/gray-wolves-survived-the-ice-age-by-changing-their-diet/" target="_blank" rel="noreferrer noopener">gray wolves</a>?



Dr. Nathan Wales, also from the University of York’s Department of Archaeology, explained further. 



“We know grey wolves have been around as a species for hundreds of thousands of years, based on skeletal remains from palaeontological sites, and researchers have done DNA testing of some of those remains to understand how the population changed over time," he shared. 



He added that the soft tissues preserved in the Tumat cubs gives another, fascinating way of investigating the wolf evolutionary line. 



“We can see that their diets were varied, consisting of both animal meat and plant life, much like that of modern wolves," he said, "and we have an insight into their breeding behaviors too. The pair were sisters and likely being reared in a den and cared for by their pack – all common characteristics of breeding and raising of offspring in wolves today."



It is common for modern wolves to have larger litters than two, and it is possible that the Tumat cubs had siblings that escaped the fate of the unfortunate sisters. Or perhaps there will be more of the litter hidden in the permafrost nearby. 



Dr. Wales also commented on the fact that wooly rhinoceros remains were found in the cubs' stomachs. 



“The hunting of an animal as large as a wooly rhinoceros, even a baby one, suggests that these wolves are perhaps bigger than the wolves we see today, but still consistent in many ways, because wolves still tend to hunt easy prey while some of the pack is engaged in cub rearing.”



<h2 class="wp-block-heading" id="h-the-dog-puzzle-remains">The dog puzzle remains</h2>



This study does more than shed light on two ancient cubs. It also leaves an open question: When and where did dogs emerge from their wolf ancestors?



So, while the Tumat "puppies" are not the key to unlocking the origin of domestic dogs, they are a vital piece of the puzzle. And somewhere, buried in the frost or hidden in ancient sediments, the first true dog still waits to be found.



The full study was published in the journal <a href="https://www.cambridge.org/core/journals/quaternary-research/article/abs/multifaceted-analysis-reveals-diet-and-kinship-of-late-pleistocene-tumat-puppies/B4DC077D8A6C18FD96F7E8E0D3428A46" target="_blank" rel="noreferrer noopener">Quaternary Research</a>.



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Famous 'ice-age puppies' are not actually dogs, according to new study

Two small cubs that died more than 14,000 years ago,...

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...

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...

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...

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...

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...

In the face of global biodiversity loss, protected areas have emerged as a crucial conservation strategy. These regions are set aside to limit human interference and provide wildlife with a safe space. 



Conservationists often focus on species counts when measuring success. But are these protected zones doing enough to preserve the entire structure of ecosystems?



This question is at the heart of a new study from <a href="https://www.swansea.ac.uk" target="_blank" rel="noreferrer noopener">Swansea University</a>. Instead of focusing only on species richness, the researchers examined how protected areas affect the complex interactions between species. 



These species interactions - especially predator-prey relationships - build the food webs that make <a href="https://www.earth.com/news/extinction-by-design-should-we-genetically-erase-harmful-species/" target="_blank" rel="noreferrer noopener">ecosystems</a> stable and functional.



<h2 class="wp-block-heading" id="h-species-count-is-not-enough-nbsp">Species count is not enough&nbsp;</h2>



Species richness is important. However, <a href="https://www.earth.com/news/why-millions-of-fungal-species-still-remain-unknown/" target="_blank" rel="noreferrer noopener">ecosystems</a> are more than a list of species. The relationships between organisms play a key role in ecological balance. A hawk hunting smaller birds or a songbird feeding on insects reflects interactions that keep ecosystems working.



The Swansea team wanted to understand if protected areas help maintain this ecological balance. They examined the structure of food webs rather than just counting how many species lived in each location. 



A food web includes all the feeding relationships between animals in a region. It shows who eats whom and how energy flows through the environment.



To conduct this study, the researchers turned to citizen science. They used data from platforms like eBird, where volunteers record bird sightings. This allowed the experts to track 509 bird species across 45 ecological networks from Spain to Finland.



<h2 class="wp-block-heading" id="h-food-webs-inside-and-outside-reserves">Food webs inside and outside reserves</h2>



Using this large database, the team combined observational bird records with known predator-prey links. For example, if a particular raptor feeds on smaller birds, that relationship was mapped. Each network captured the structure of a local bird community and its food web.



The team compared food webs inside protected areas to those in surrounding, non-protected <a href="https://www.earth.com/news/international-lynx-day-2025-protecting-the-silent-hunters/" target="_blank" rel="noreferrer noopener">landscapes</a>. These comparisons were not simple. 



The researchers controlled for many variables. They looked at habitat diversity, the percentage of forest and agricultural land, and levels of human pressure.



The experts also considered the designation status of the protected areas. Some zones were part of the European Bird Directives, which provide stronger conservation measures. Others had more general protections. 



These different conservation levels allowed the team to ask whether clearer goals led to better ecological outcomes.



<h2 class="wp-block-heading" id="h-protected-areas-help-in-some-places">Protected areas help in some places</h2>



So, what did the researchers find? In some cases, protected areas improved the <a href="https://www.earth.com/news/international-day-for-biological-diversity-2025-bonding-with-nature/" target="_blank" rel="noreferrer noopener">structure</a> of food webs. The networks inside protected zones tended to have more species overall. Intermediate-level species - those neither top predators nor at the bottom - were more common. 



Also, predators inside protected areas tended to be larger in body size, both at the top and middle levels of the food web.



However, not all of the results were encouraging. The length of food chains and the connectivity of species within the web did not show consistent improvement. In other words, simply having more species did not guarantee a healthier or more connected ecosystem.



The effects varied across Europe. Food webs in Spain responded differently from those in Finland or central Europe. This suggests that local conditions still matter greatly. Protection alone cannot guarantee the same results everywhere.



<h2 class="wp-block-heading" id="h-factors-behind-food-web-differences">Factors behind food web differences</h2>



What caused the variation in results? Several environmental factors played a role. Areas that were more remote generally had healthier food webs. Places with higher habitat diversity also performed better. Human pressure and the amount of nearby farmland had a strong influence too.



Interestingly, areas under the European Bird Directives showed stronger positive trends. This suggests that clearer conservation planning makes a real difference. Just designating a region as "protected" is not enough. What matters is how that protection is implemented.



Study co-author Dr. Miguel Lurgi, who leads the Computational Ecology Lab, emphasized the significance of the research. 



“Studies like ours highlight the complexity of conservation action and the importance of considering key aspects of biodiversity beyond species richness, such as ecological interactions and the tangled networks that they form, into biodiversity assessments,” noted Dr. Lurgi.



“These networks not only structure communities and enable their persistence, but they also play important roles in the functions that ecosystems fulfil in nature.”



<h2 class="wp-block-heading" id="h-we-must-protect-species-and-their-roles-nbsp">We must protect species and their roles&nbsp;</h2>



This study challenges a common assumption in conservation planning. Many projects measure success by the number of species saved. The research shows that relationships between species are equally vital. 



Protecting one bird species is good. Ensuring that it still plays its ecological role - as predator, prey, or pollinator - is better.



Protected areas clearly help in some ways. They offer space for species to live and grow. But without active planning, their impact on food webs may fall short. Conservation needs to think about networks, not just numbers.



By looking at predator-prey relationships, this research opens a path to more holistic conservation strategies. It also highlights the value of citizen science. 



Platforms like eBird make this kind of large-scale ecological work possible. Every birdwatcher’s observation helps build a clearer picture of how our ecosystems function.



<h2 class="wp-block-heading" id="h-protected-areas-need-better-plans">Protected areas need better plans</h2>



Europe's protected areas are not failing, but they are not universally succeeding either. They need tailored strategies, grounded in ecological data. Simple protection does not always support complex ecosystems.



This study gives policymakers a reason to refine their approaches. If the goal is to protect ecosystems, not just individual species, then conservation must shift. It must include ecological interactions, food web structures, and the subtle forces that hold nature together.



As this research shows, conservation cannot afford to stay simple. Nature is complex. Our strategies must match that complexity.



The study is published in the journal <a href="https://royalsocietypublishing.org/doi/10.1098/rspb.2025.0614" target="_blank" rel="noreferrer noopener">Proceedings of the Royal Society B Biological Sciences</a>.



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Protected areas don't always protect food webs

In the face of global biodiversity loss, protected areas have...

A small team of researchers has reported a striking achievement: they succeeded in raising a mouse that came from two male parents, and it grew into a healthy adult. Their work unveils a set of genetic changes that overcomes the imprinting barriers that typically block such development.



Scientists in various fields have tried for years to figure out how paternal-only DNA could sustain a mammal through all stages of life. 



<h2 class="wp-block-heading" id="h-understanding-gene-imprinting">Understanding gene imprinting</h2>



<a href="https://www.genome.gov/genetics-glossary/Genetic-Imprinting" target="_blank" rel="noreferrer noopener">Biological imprinting</a> is an inherited pattern of <a href="https://www.genome.gov/genetics-glossary/Gene-Expression" target="_blank" rel="noreferrer noopener">gene expression</a>. It involves certain genes getting turned on or off depending on whether they come from the father or the mother. 



Researchers found that if you adjust a selection of these imprinting genes, you can open the door for unique reproductive feats, such as an embryo that starts with only paternal cells.



“This work will help to address a number of limitations in stem cell and regenerative medicine research,” explains <a href="http://english.ioz.cas.cn/sourcedb/scs/202310/t20231030_431101.html" target="_blank" rel="noreferrer noopener">Wei Li</a> of the Chinese Academy of Sciences in Beijing. 



In this case, the scientists homed in on key sections of DNA that are known to control fetal growth and viability.



<h2 class="wp-block-heading" id="h-what-this-means-for-biology">What this means for biology</h2>



When a mouse embryo is formed in the usual way, paternal and <a href="https://www.earth.com/news/pregnancy-stress-may-have-lasting-effects-on-fetal-development/" target="_blank" rel="noreferrer noopener">maternal DNA</a> come together. That combination produces a precise balance of imprinted genes. 



In paternal-only embryos, certain growth-related genes can become overstimulated, but the team was able to selectively modify them so these embryos could mature.



“These findings provide strong evidence that imprinting abnormalities are the main barrier to mammalian unisexual reproduction,” said Qi Zhou, co-lead of this study. 



By re-engineering the problematic gene regions, the researchers made it possible for two sets of <a href="https://www.earth.com/news/y-chromosome-is-disappearing-may-already-be-causing-problems-for-men/" target="_blank" rel="noreferrer noopener">male chromosomes</a> to support a developing mouse.



<h2 class="wp-block-heading" id="h-therapeutic-ideas">Therapeutic ideas</h2>



A number of genetic and metabolic disorders in humans stem from errors in imprinting. Scientists have asked whether strategies used here might be adapted to correct imprinting problems that cause diseases in people.



One potential target is <a href="https://www.ncbi.nlm.nih.gov/books/NBK425128/" target="_blank" rel="noreferrer noopener">KCNK9</a>, which has been linked to <a href="https://pubmed.ncbi.nlm.nih.gov/18678320/" target="_blank" rel="noreferrer noopener">Birk-Barel syndrome</a>. Precise gene editing of such imprinting sites could help in the design of improved treatments for these rare disorders.



In practice, these ideas may take time to progress. Mouse models are often a first step in studying how imprinting influences development. 



The more scientists understand about restoring the right imprinting patterns, the closer they might come to tackling certain medical conditions.



<h2 class="wp-block-heading" id="h-gene-imprinting-implications">Gene imprinting implications</h2>



The modified imprinting genes not only allowed bi-paternal mice to survive to adulthood, they also improved the efficiency of stem cells used in the process. 



The researchers reported that these <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC1181832/" target="_blank" rel="noreferrer noopener">engineered embryonic stem cells</a> were about twice as likely to develop into full-term pups compared to unmodified cells.



This improved developmental stability could change how scientists approach cloning. Currently, cloned animals often suffer from low survival rates and severe abnormalities, in part due to faulty imprinting. 



Fixing imprinting errors ahead of time might make future cloning methods more reliable, especially in complex mammals like primates.



<h2 class="wp-block-heading" id="h-ethical-considerations">Ethical considerations</h2>



Questions often arise about how these approaches could extend to humans. 



According to guidelines from the International Society for Stem Cell Research (<a href="https://www.isscr.org/guidelines" target="_blank" rel="noreferrer noopener">ISSCR</a>), heritable genome editing is not currently allowed for human reproductive purposes because it is considered unsafe.



Researchers continue to examine these practices in animal models before even considering steps that approach human application. Investigators involved in this work remain cautious.&nbsp;



While a <a href="https://www.earth.com/news/scientists-inject-40000-year-old-neanderthal-dna-gli3-gene-into-mice-with-incredible-results/">mouse</a> with two fathers has captured headlines, translating similar methods to people is a bigger leap. 



The focus remains on unraveling how imprinted genes function, and how targeted interventions might fix imprinting-related diseases down the road.



<h2 class="wp-block-heading" id="h-next-questions">Next questions</h2>



There is still room to explore how best to refine these <a href="https://www.earth.com/news/fathers-have-a-surprising-influence-on-their-babys-birth-weight/" target="_blank" rel="noreferrer noopener">genetic strategies</a> to improve survival rates and lessen the chance of complications. 



Specialists are also looking at future animal models to see if placental differences, organ development, or immune responses undergo subtle changes when imprinting is modified. 



Some foresee that data gleaned from these methods will shape the next generation of gene-editing research.



Ongoing studies point to a need for caution. Issues like longevity, fertility, and normal physiology require much deeper evaluation. 



Still, scientists see value in applying these insights to refine cloning and enhance studies of embryonic stem cells. Even partial solutions could inform safer protocols for regenerating cells and tissues in healthcare settings.



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This <a href="https://www.cell.com/cell-stem-cell/fulltext/S1934-5909(25)00005-0?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS1934590925000050%3Fshowall%3Dtrue">breakthrough</a> was led by <a href="http://english.ioz.cas.cn/sourcedb/scs/202310/t20231030_431101.html" target="_blank" rel="noreferrer noopener">Wei Li</a> of the <a href="https://english.cas.cn/" target="_blank" rel="noreferrer noopener">Chinese Academy of Sciences in Beijing</a> and Qi Zhou of the same institution, with further input from collaborators at <a href="https://www.sysu.edu.cn/sysuen/" target="_blank" rel="noreferrer noopener">Sun Yat-sen University</a>.



The study is published in <a href="https://www.sciencedirect.com/science/article/pii/S1934590925000050" target="_blank" rel="noreferrer noopener">Cell Stem Cell</a>.



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Scientists raised a mouse born from two male parents to adulthood for the first time

A small team of researchers has reported a striking achievement:...

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