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

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

The world’s seas have long acted as a planetary safety net, soaking up excess heat and roughly a quarter of all human-generated carbon dioxide. 



Yet this crucial buffer is anything but uniform. Some waters capture carbon, others release it, and the balance can swing in a matter of days.



Until now, most global maps blurred those variations into month-long snapshots at coarse, 100-kilometer grids. 



A new satellite-driven product called <a href="https://essd.copernicus.org/articles/13/777/2021/">OceanSODA-ETHZ</a> changes that picture, offering eight-day updates at 25-kilometer resolution and revealing the ocean <a href="https://www.earth.com/news/earths-carbon-sinks-are-being-pushed-to-their-limits/">carbon sink</a> in unprecedented detail.



<h2 class="wp-block-heading" id="h-satellites-fill-ocean-carbon-gaps">Satellites fill ocean carbon gaps</h2>



Direct readings of surface-water CO2 come from ships and buoys, leaving vast gaps in space and time.



“Increasing the resolution of these global datasets is challenging because the number of direct measurements of carbon dioxide at the ocean’s surface is rather sparse across all regions and times,” explained project co-leader Nicolas Gruber of ETH Zurich.



To fill those gaps, Gruber’s team paired the in situ data with a suite of Earth-observation satellites that sense <a href="https://www.earth.com/news/humans-are-substantially-changing-the-seasons-of-the-ocean/">sea-surface temperature</a>, color, wind, and more - variables tightly linked to how much CO2 water can hold.



Feeding that information into a cascade of machine-learning algorithms produced a fine-grained, eight-day global mosaic.



“This new version maps the parameters of the ocean carbon system every eight days at a resolution of about 25 by 25 kilometers, more than 30 times finer than previous products,” Gruber said.



“A critical part of the approach is the use of satellite data, which provides detailed information to interpolate the measurements in time and space.”



<h2 class="wp-block-heading" id="h-satellites-track-ocean-carbon-changes">Satellites track ocean carbon changes</h2>



Presented this week at <a href="https://lps25.esa.int/">ESA’s Living Planet Symposium</a>, the dataset already highlights dramatic short-term swings. 



An animation released by the team tracks the 2017 Atlantic <a href="https://www.earth.com/news/how-hurricanes-help-oceans-fight-climate-change/">hurricane</a> season, when storms such as Maria and Irma churned deep, carbon-rich waters to the surface.



<figure class="wp-block-embed is-type-video is-provider-youtube wp-block-embed-youtube wp-embed-aspect-16-9 wp-has-aspect-ratio"><div class="wp-block-embed__wrapper">
https://youtu.be/cEUvoY8krHM?si=cX1giVtLnycyFKqr
</div><figcaption class="wp-element-caption">Animation generated using the new OceanSODA-ETHZv2 product by Luke Gregor, Jamie Shutler and Nicolas Gruber</figcaption></figure>



In the visualization, red plumes - areas where the sea outgasses CO2 - flare beneath the swirling wind arrows, then fade as cooler, oxygen-laden surface layers return.



Jamie Shutler from the University of Exeter, while not involved in developing the product, is already using it for storm studies.



“Thanks to its fine detail, the dataset can help us separate and understand the influence of events like hurricanes - where deep water, often high in carbon, can be forced to rise to the surface - which can cause sudden spikes or changes in surface ocean carbon dioxide levels,” said Shutler.



<h2 class="wp-block-heading" id="h-a-new-view-of-ocean-acidification">A new view of ocean acidification</h2>



Every molecule of CO2 that the ocean absorbs reacts with seawater, lowering pH and shifting carbonate chemistry in ways that erode coral skeletons, thin oyster shells, and alter plankton communities.



Until now, researchers tracking this “other CO2 problem” relied on sparse records or coarse climatologies. 



OceanSODA-ETHZ delivers near-real-time fields of surface pH and carbonate ions, letting scientists watch <a href="https://www.earth.com/news/ocean-acidification-is-spreading-into-deeper-waters/">acidification</a> pulses unfold as upwelling, rainfall, or melting sea ice change local chemistry.



Because the product also extends back to 1985, analysts can mine four decades of fine-scale variability to see where buffers are weakening and hotspots are emerging. 



Those insights can feed into fisheries management, coastal planning, and global carbon-budget assessments.



<h2 class="wp-block-heading" id="h-esa-powers-new-ocean-maps">ESA powers new ocean maps</h2>



The dataset is the latest deliverable from <a href="https://eo4society.esa.int/">ESA’s FutureEO “Science for Society” program</a>, which funds innovative uses of satellite records.



“The fact that we can use this method to gain new insights into the exchange of carbon dioxide between the ocean and atmosphere - and on the ocean acidification altogether - is a great step forward in ocean science,” said Roberto Sabia, an ocean scientist at <a href="https://www.esa.int/Applications/Observing_the_Earth">ESA Earth-Observation</a>. 



Gruber and colleagues emphasize that OceanSODA-ETHZ is not a static atlas but a living product that can assimilate new ship measurements and leverage upcoming satellite missions.



Higher-resolution sensors such as <a href="https://pace.gsfc.nasa.gov/">NASA’s PACE</a> and <a href="https://www.esa.int/Applications/Observing_the_Earth/Copernicus/Copernicus_Sentinel_Expansion_missions">ESA’s Copernicus Expansion</a> promise even clearer views of <a href="https://www.earth.com/news/plankton-help-predict-ocean-biodiversity-losses/">plankton</a> blooms, sea-surface roughness, and dissolved organic matter - all factors that modulate carbon exchange.



<h2 class="wp-block-heading" id="h-forecasts-of-regional-carbon-uptake">Forecasts of regional carbon uptake</h2>



Ultimately, the goal is to couple these detailed maps with ocean-atmosphere models, yielding short-term forecasts of regional carbon uptake akin to daily weather predictions.



Such tools could alert coastal managers when acidification thresholds are likely to be breached or help negotiators refine national emissions budgets by tracking natural carbon sinks more precisely.



For now, the new product already reshapes our understanding of the ocean’s role in moderating climate. 



Where earlier charts smoothed over crucial dynamics, OceanSODA-ETHZ reveals a living, breathing carbon landscape - one where swirling eddies, roaring storms, and shifting <a href="https://www.earth.com/news/small-ocean-currents-play-a-huge-role-in-earths-climate/">currents</a> all leave their stamp on the planet’s most important carbon reservoir.



Image Credit: ESA



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Satellites reveal how oceans absorb carbon in unprecedented detail

The world’s seas have long acted as a planetary safety...

Fire has licked the planet’s surface for more than 400 million years, scorching forests, clearing grasslands, and lofting smoke into the upper air. Yet pinning down when people stopped fearing flames and started steering them has been surprisingly hard.



A fresh <a href="https://www.pnas.org/doi/10.1073/pnas.2500042122" target="_blank" rel="noreferrer noopener">analysis</a> of a 300,000‑year‑old sediment core pulled from the East China Sea finds a sharp surge in soot about 50,000 years ago, a signal that stands apart from normal climate‑driven wildfire patterns.



The work, led by Dr. Zhao Debo at the <a href="http://english.qdio.cas.cn/" target="_blank" rel="noreferrer noopener">Institute of Oceanology</a>, Chinese Academy of Sciences, together with partners in Germany and France, strings together chemical, archaeological, and climate evidence into one timeline.



“Our findings challenge the widely held belief that humans only began influencing the <a href="https://www.earth.com/news/ideas-traveled-farther-than-people-in-the-early-days-of-farming/">environment</a> with fire in the recent past, during the Holocene,” said Dr. Zhao Debo.



<h2 class="wp-block-heading" id="h-when-humans-began-using-fire">When humans began using fire</h2>



Researchers tracked <a href="https://www.nature.com/articles/s43247-024-01343-5" target="_blank" rel="noreferrer noopener">pyrogenic carbon</a>, the charred plant residue left when biomass burns incompletely, because rivers flush those tiny black flecks into coastal mud where they store a record of past fires.



Between 60,000 and 45,000 years ago that charcoal fraction doubled, then stayed high. The jump broke its long connection to East Asian monsoon strength, showing that weather alone could not explain the flames.



Parallel charcoal peaks in Europe, Southeast Asia, and the Papua New Guinea–Australia corridor line up with the same window, pointing to a continent‑scale shift rather than scattered lightning <a href="https://www.earth.com/news/birth-of-farming-driven-by-humans/">strikes</a>.



<h2 class="wp-block-heading" id="h-fire-use-spreads-across-continents">Fire use spreads across continents</h2>



Archaeological <a href="https://www.science.org/content/article/more-45000-years-ago-modern-humans-ventured-neanderthal-territory-here-s-what-happened" target="_blank" rel="noreferrer noopener">hearths</a> from Bulgaria’s <a href="https://visitbulgaria.com/bacho-kiro-cave/" target="_blank" rel="noreferrer noopener">Bacho Kiro Cave</a> to northern Australia’s <a href="https://www.britannica.com/place/Madjedbebe" target="_blank" rel="noreferrer noopener">Madjebebe</a> site cluster inside the same interval, confirming that <a href="https://www.science.org/content/article/more-45000-years-ago-modern-humans-ventured-neanderthal-territory-here-s-what-happened" target="_blank" rel="noreferrer noopener">campfires</a> had become routine parts of daily life.



Genetic <a href="https://www.nature.com/articles/s41586-025-09154-0" target="_blank" rel="noreferrer noopener">studies</a> trace almost all non‑African ancestry to a single successful wave of Homo sapiens that left Africa about 50,000 years ago, matching the charcoal timeline.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/humans_fire_early-homo-sapiens_map-sites_credit-IOCAS_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/humans_fire_early-homo-sapiens_map-sites_credit-IOCAS_1s.webp" alt="Fire history of Europe, East Asia, Southeast Asia and Papua New Guinea–Australia and age distribution of archaeological sites since the last 300,000 years. Credit: IOCAS" class="wp-image-1976185"/></a><figcaption class="wp-element-caption">Fire history of Europe, East Asia, Southeast Asia and Papua New Guinea–Australia and age distribution of archaeological sites since the last 300,000 years. Click image to enlarge. Credit: IOCAS</figcaption></figure>



While earlier <a href="https://www.earth.com/news/evidence-of-ancient-plant-farming-found-in-east-africa/">humans</a> played with sparks, evidence for habitual fire stretches back at least 250,000 years in Europe, those earlier experiments were local and intermittent. The new record shows the first moment when fire use scales with population growth.



<h2 class="wp-block-heading" id="h-migration-cold-nights-and-campfires">Migration, cold nights, and campfires</h2>



The out‑of‑Africa travelers trekked into ice‑age Eurasia where nights dipped well below freezing. Fire kept predators away, cooked meat, dried hides, and allowed late‑night tool making.



“Even during the Last Glaciation, the use of fire had probably started to reshape ecosystems and carbon fluxes,” added <a href="http://english.qdio.cas.cn/people/jzg/202208/t20220803_310174.html" target="_blank" rel="noreferrer noopener">Professor Wan Shiming</a>, a co‑author on the study.



Controlled flame also opened new food groups. Roasting tubers breaks down starches, and heated stone cracks to yield sharper blades, advantages that likely boosted survival odds for the migrants.



<h2 class="wp-block-heading" id="h-burning-added-carbon-to-land-and-ocean">Burning added carbon to land and ocean</h2>



Modern wildfires already release between 116 and 385 teragrams of <a href="https://www.nature.com/articles/s41598-017-10455-2" target="_blank" rel="noreferrer noopener">pyrogenic carbon</a> to land and sea each year, a sizable slice of the global carbon ledger. 



When ancient people started burning wood on purpose, they nudged that ledger long before industrial smokestacks appeared.



Charcoal is stable. Some pieces survive for millennia in soils, some drift as <a href="https://www.pnas.org/doi/10.1073/pnas.2305030121" target="_blank" rel="noreferrer noopener">dissolved black carbon</a> into the deep ocean where currents can store it for thousands of years. 



By pushing extra charcoal into these sinks, early fire managers may have offset part of the carbon dioxide they released.



Climate models that begin counting human impacts only with <a href="https://www.earth.com/news/cave-discovery-of-ancient-avocados-could-rescue-a-global-crop/">farming</a> or factories might therefore miss a slow, earlier perturbation that started when nightly campfires became normal.



<h2 class="wp-block-heading" id="h-early-human-fire-use-shaped-climate">Early human fire use shaped climate</h2>



The <a href="https://www.sciencedirect.com/science/article/pii/S2212682112000261" target="_blank" rel="noreferrer noopener">East China Sea</a> record shows that environmental influence is not a recent human monopoly. Small groups with stone tools and wooden spears were already altering regional fire regimes and, in turn, the carbon cycle.



That insight reframes today’s policy debates. If early people changed atmospheric chemistry with nothing but sticks and sparks, eight billion of us wielding fossil fuels carry far more leverage, and responsibility, than any ancestral hunter‑gatherer could imagine.



Fire management still shapes global climate in modern times. Prescribed burns reduce fuel loads but also emit smoke; savanna fires in Africa and Australia pulse <a href="https://www.earth.com/news/worlds-first-greenhouse-gas-detecting-satellite-is-now-in-orbit/">greenhouse gases</a> each dry season; boreal megafires now send record carbon plumes aloft. 



Understanding the deep history of intentional burning helps calibrate those modern choices. Fifty thousand years later we still gather around flames, but the scale has ballooned from glowing embers to global power grids.



The study is published in <a href="https://www.pnas.org/doi/10.1073/pnas.2500042122" target="_blank" rel="noreferrer noopener">Proceedings of the National Academy of Sciences</a>.



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Humans learned to use and control fire much earlier than previously believed

Fire has licked the planet’s surface for more than 400 million...

The James Webb Space Telescope has delivered the clearest, deepest images yet of the Bullet Cluster, unveiling thousands of faint, distant galaxies and offering the most precise map of dark matter in this iconic colliding galaxy cluster.



“With <a href="https://www.earth.com/news/thousands-of-galaxies-revealed-in-a-single-webb-image/">Webb</a>’s observations, we carefully measured the mass of the Bullet Cluster with the largest lensing dataset to date, from the galaxy clusters’ cores all the way out to their outskirts,” said lead author Sangjun Cha, a PhD student at <a href="https://www.yonsei.ac.kr/en_sc/index.do">Yonsei University</a> in Seoul. 



Previous studies relied on less lensing data, leading to less precise estimates of the system’s mass.



“Webb’s images dramatically improve what we can measure in this scene -&nbsp; including pinpointing the position of invisible particles known as dark matter,” said co-author Kyle Finner, an assistant scientist at <a href="https://www.caltech.edu/">Caltech</a>. 



<h2 class="wp-block-heading" id="h-how-light-shows-the-dark">How light shows the dark</h2>



The Bullet Cluster is made of two massive galaxy clusters bound by <a href="https://www.earth.com/news/desi-gravity-study-new-discovery-proves-einstein-right-again/">gravity</a>. It acts as a natural gravitational lens that magnifies background galaxies.



James Jee, a professor at Yonsei University and research associate at UC Davis, is a co-author of the study. “Gravitational lensing allows us to infer the distribution of dark matter,” he said.



To visualize this effect, Jee compares it to ripples on a pond. You can't see the clear water unless there are ripples that distort the shapes of the pebbles below - just as dark matter distorts the light from galaxies behind it.



By measuring thousands of galaxies, the scientists used Webb’s images to weigh visible and invisible mass in the cluster. 



The team also mapped the faint glow of intracluster stars - those not bound to any single galaxy. These drifting stars may closely trace dark matter.



<h2 class="wp-block-heading" id="h-webb-s-dark-matter-reveal">Webb’s dark matter reveal</h2>



Webb’s observations produced a layered view, combining near-infrared data with X-ray imagery from <a href="https://www.nasa.gov/mission/chandra-x-ray-observatory/">NASA’s Chandra X-ray Observatory</a>, revealing hot gas in pink, the bullet shape in the cluster, and the newly refined dark matter distribution in blue.



“We confirmed the intracluster light can be a reliable tracer of dark matter, even in a highly dynamic environment like the Bullet Cluster,” Cha said. 



This strengthens the case that these unbound stars closely trace dark matter’s invisible scaffolding.



The new map reveals detailed structure, including an asymmetric mass region on the left side of the larger cluster. This feature indicates prior collisions that have left behind signatures in the distribution of matter.



<h2 class="wp-block-heading" id="h-mysterious-nature-of-dark-matter">Mysterious nature of dark matter </h2>



Dark matter does not emit, reflect, or absorb light, making it notoriously difficult to study. Yet the Bullet Cluster offers a rare laboratory, showing dark matter separated from hot gas during a cosmic collision while still aligning with the galaxies.



“As the <a href="https://www.earth.com/news/titanic-galaxy-cluster-collision-defies-all-current-understanding-of-the-universe/">galaxy clusters</a> collided, their gas was dragged out and left behind, which the X-rays confirm,” Finner explained. “Webb’s observations show that dark matter still lines up with the galaxies - and was not dragged away.”



The results set tighter constraints on the possibility of dark matter particles interacting with each other. They support theories that dark matter passes through itself without friction, consistent with its mysterious and ghostly nature.



<h2 class="wp-block-heading" id="h-clues-to-a-chaotic-past"><a></a>Clues to a chaotic past</h2>



The elongated mass and clumps in the new map hint at a more complex history for the Bullet Cluster, suggesting multiple collisions over billions of years.



“A more complicated scenario would lead to a huge asymmetric elongation like we see on the left,” Jee said.



The Bullet Cluster, located in the Carina <a href="https://www.earth.com/news/super-jupiter-discovered-in-the-great-bear-constellation/">constellation</a> 3.8 billion light-years from Earth, is so massive that even Webb’s powerful NIRCam could only capture part of it.



“It’s like looking at the head of a giant,” Jee explained. “Webb’s initial images allow us to extrapolate how heavy the whole 'giant' is, but we’ll need future observations of the giant’s whole 'body' for precise measurements.”



<h2 class="wp-block-heading" id="h-future-missions-deeper-maps">Future missions, deeper maps</h2>



NASA’s upcoming <a href="https://www.earth.com/news/nasas-roman-space-telescope-hopes-to-solve-the-dark-matter-mystery/">Nancy Grace Roman Space Telescope</a>, launching by May 2027, will complement Webb’s discoveries with wide-field near-infrared imaging. 



The Roman telescope will enable complete mass estimates of the Bullet Cluster and allow scientists to simulate its ancient collision in detail.



“With Roman, we will have complete mass estimates of the entire Bullet Cluster, which would allow us to recreate the actual collision on computers,” Finner said.



Through these detailed observations, Webb is enriching our understanding of dark matter. It’s also advancing knowledge of how massive structures form and evolve, offering a clearer view of the hidden forces shaping the cosmos.



The study is published in the <a href="https://iopscience.iop.org/article/10.3847/2041-8213/add2f0">Astrophysical Journal Letters</a>.



Image Credit: NASA, ESA, CSA, STScI, CXC



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Webb telescope uncovers secrets of dark matter in cosmic collision zone

The James Webb Space Telescope has delivered the clearest, deepest...

Coffee is prized for its taste and mental boost. A new study shows that caffeine may also fine‑tune the internal clock that makes cells grow old.



Researchers observed that yeast aged more slowly when caffeine altered the same energy pathways that help human cells <a href="https://www.earth.com/news/organ-aging-can-predict-diseases-decades-in-advance/">survive</a> under stress.



<h2 class="wp-block-heading" id="h-caffeine-slows-aging-in-yeast-cells">Caffeine slows aging in yeast cells</h2>



Dr. Charalampos (Babis) Rallis of <a href="https://www.qmul.ac.uk/">Queen Mary University of London</a> focused on the yeast species Schizosaccharomyces pombe because its DNA repair and growth controls echo our own. 



The team logged changes in <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC9139625/" target="_blank" rel="noreferrer noopener">chronological lifespan</a>, the length of time that non‑dividing cells stay viable, then mapped the molecular traffic that caffeine set in motion.



“This is our most exciting find to date,” said Dr. Rallis. The results point to a fuel‑sensing <a href="https://www.earth.com/news/healthy-aging-how-some-people-live-past-100-years/">pathway</a> that kicks in when nutrients dip, mirroring how people burn stored energy between meals.&nbsp;



<h2 class="wp-block-heading" id="h-yeast-helps-us-understand-aging">Yeast helps us understand aging</h2>



Fission yeast may seem worlds apart from humans, but it shares many core <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC4772020/" target="_blank" rel="noreferrer noopener">regulatory pathways</a> found in our cells. Systems like <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC2779044/" target="_blank" rel="noreferrer noopener">AMPK</a> and <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC3241408/" target="_blank" rel="noreferrer noopener">TOR</a> have been conserved over hundreds of millions of years because they work so well.



This makes yeast an ideal testing ground for decoding how compounds like caffeine affect <a href="https://www.earth.com/news/scientists-are-experimenting-with-new-approach-to-fight-and-stop-human-aging-necrosis/">lifespan</a> and stress response. What happens in a petri dish often sparks questions that ripple out to animal models and eventually to people.



<h2 class="wp-block-heading" id="h-how-caffeine-may-slow-aging">How caffeine may slow aging</h2>



The key player is AMPK, an enzyme that "notices" when the cell’s ATP (energy) balance tilts toward empty and then shifts metabolism to survival mode. 



“Caffeine helps flip that switch,” said <a href="https://scholar.google.com/citations?user=913OCBIAAAAJ&amp;hl=en" target="_blank" rel="noreferrer noopener">Dr. John‑Patrick Alao</a>, the postdoctoral scientist who ran the experiments.



Earlier <a href="https://pubmed.ncbi.nlm.nih.gov/23551936/" target="_blank" rel="noreferrer noopener">work</a> suggested caffeine blocked <a href="https://pubmed.ncbi.nlm.nih.gov/23551936/" target="_blank" rel="noreferrer noopener">TOR</a>, a growth promoter, but new data reveal the compound reaches TOR indirectly by first waking up AMPK. 



Cells then slow growth, patch damaged DNA, and boost antioxidant defenses, the very responses that lengthen life in many lab organisms.



<h2 class="wp-block-heading" id="h-caffeine-and-metformin-use-same-pathway">Caffeine and metformin use same pathway</h2>



<a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC6779524/" target="_blank" rel="noreferrer noopener">Metformin</a>, the common diabetes drug, also charges AMPK and is being tested as a geroprotector in humans. The overlap hints that coffee’s benefits may parallel those seen in metformin cohorts, though dosage and metabolism differ widely.



Both agents dial back inflammation, clear out faulty proteins through autophagy, and keep insulin signaling from running too hot. 



If future trials confirm safety, researchers may combine low‑dose caffeine with metformin analogs to see whether their effects stack without side effects.



<h2 class="wp-block-heading" id="h-caffeine-helps-manage-cell-stress">Caffeine helps manage cell stress</h2>



The AMPK pathway doesn’t just manage fuel, it also guides how cells respond to <a href="https://www.ncbi.nlm.nih.gov/medgen/222489" target="_blank" rel="noreferrer noopener">genotoxic stress</a>, such as radiation or chemicals that harm DNA. 



The yeast data showed caffeine increased sensitivity to DNA damage in some mutants, revealing AMPK's role in damage response.



This dual role, energy control and DNA repair, suggests that caffeine tunes both survival and quality control systems. 



It’s part of a wider stress adaptation strategy that has been conserved across <a href="https://www.earth.com/news/scientists-discover-a-protein-that-reverses-cellular-aging/">evolution</a>, and is now offering new angles for anti-aging research.



<h2 class="wp-block-heading" id="h-people-who-drink-coffee-may-live-longer">People who drink coffee may live longer</h2>



Observational work involving hundreds of thousands of adults links two to four cups of coffee daily with <a href="https://pubmed.ncbi.nlm.nih.gov/31055709/" target="_blank" rel="noreferrer noopener">lower all‑cause mortality</a>. 



Separate <a href="https://pubmed.ncbi.nlm.nih.gov/34468722/" target="_blank" rel="noreferrer noopener">analyses</a> in Asian populations find similar protection against heart disease and several cancers.



Because these studies track behavior, not biology, confounding factors like diet, exercise, and income can cloud cause and effect. 



The yeast data now give those population numbers a plausible mechanism anchored in cell chemistry, without the noise of other factors.



<h2 class="wp-block-heading" id="h-future-research-on-caffeine-and-aging">Future research on caffeine and aging</h2>



Yeast tolerate caffeine levels far above a latte, so dose matters when translating findings to people. 



Human AMPK is embedded in tissues that react differently, so benefits in muscle may come at a cost elsewhere if DNA repair stalls during caffeine peaks.



High caffeine can raise blood pressure, trigger anxiety, and interfere with sleep - processes that can speed cell aging if left unchecked. 



Clinical trials that track AMPK activation, cardiovascular markers, and cognitive scores together will be needed before doctors advise specific amounts.



<h2 class="wp-block-heading" id="h-the-role-of-diet-and-exercise">The role of diet and exercise </h2>



Exercise is one of the most well-known ways to activate AMPK in humans. When muscles burn through energy during physical activity, this pathway turns on to help cells adapt and recover.



Certain foods, including those high in polyphenols like berries and green tea, may also give AMPK a nudge. 



Understanding how diet and lifestyle naturally influence this system could lead to everyday habits that support healthy aging.



<h2 class="wp-block-heading" id="h-a-healthy-lifestyle-matters">A healthy lifestyle matters</h2>



For now, moderate coffee remains a safe pleasure that lines up with epidemiology and basic science. Sleepless nights and energy drinks loaded with sugar still pose risks that no enzyme tweak can erase.



Nutrient‑sensing pathways such as AMPK give researchers a roadmap for therapies, yet lifestyle, steady sleep, balanced diet, and movement, keep the road free of potholes. 



The next wave of studies may explore caffeine analogs that lock onto AMPK with precision, separating the perks from the jitters.



The study is published in <a href="https://microbialcell.com/researcharticles/2025a-alao-microbial-cell/" target="_blank" rel="noreferrer noopener">Microbial Cell</a>.



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Scientists learn that caffeine could slow cellular aging under the right conditions

Coffee is prized for its taste and mental boost. A...

A faded coffee ring on a countertop can vanish with a few swipes of a melamine “magic” sponge. Most of those swipes leave behind something you cannot see, and it may follow the water straight to your faucet.



<a href="https://hjxy.nju.edu.cn/English/Faculty/FulltimeTeacher/DepartmentofEnvironmentalSciences/Professors/20230328/i240942.html" target="_blank" rel="noreferrer noopener">Dr. Rong Ji</a> of Nanjing University studied these invisible leftovers and calls them a silent waste stream escaping from every kitchen.



<h2 class="wp-block-heading" id="h-understanding-melamine-in-sponges">Understanding melamine in sponges</h2>



Melamine is an industrial chemical that shows up in all sorts of places - kitchenware, laminates, even some types of insulation. 



It’s prized for its durability, heat resistance, and <a href="https://www.earth.com/news/are-we-breathing-cancer-causing-chemicals-in-our-cars/">fire-retardant</a> properties, especially in products like melamine-formaldehyde resin. 



That’s the slick, hard plastic you find in dishes and countertops. In the manufacturing world, it’s a real workhorse. 



But when melamine crosses into the food chain, usually through contaminated products or packaging, that’s when trouble starts.



The problem? The human body can’t properly break it down. Ingesting melamine, especially in large amounts, can lead to <a href="https://www.earth.com/news/astronauts-can-survive-mars-space-journey-but-their-kidneys-will-be-permanently-damaged/">kidney damage</a> or failure.



<h2 class="wp-block-heading" id="h-how-a-melamine-sponge-works">How a melamine sponge works</h2>



A melamine sponge is made from poly(melamine‑formaldehyde) foam, a brittle plastic baked into a light, open‑cell lattice. Its strands are harder than they look, so the block acts like very fine sandpaper while it lifts stains.



That abrasive action also grinds the lattice itself into <a href="https://www.earth.com/news/simple-way-to-remove-microplastics-from-tap-water-home-faucet/">microplastics</a>, particles smaller than one‑fifth of an inch. The process accelerates on rougher surfaces or when extra elbow grease is applied.



<h2 class="wp-block-heading" id="h-how-much-plastic-they-shed">How much plastic they shed</h2>



Ji’s team compared several brands and densities, then placed sponges on a mechanical abrader that mimicked a vigorous scrub. They documented an average release of about 6.5 million fibers for every gram of worn sponge.



One‑tenth of a sponge’s mass can disappear during a month of regular cleaning. Using online sales data, the researchers estimated 4.9 trillion fibers could wash down drains worldwide each month at that wear rate.



“The sponge wear could release 6.5 million microplastic fibers per gram. Our study reveals a hitherto unrecognized source of environmental microplastic fiber contamination,” wrote <a href="https://scholar.google.com/citations?user=cuWNqHkAAAAJ&amp;hl=zh-CN" target="_blank" rel="noreferrer noopener">Yu Su</a>, the study’s first author, in Environmental Science &amp; Technology.



<h2 class="wp-block-heading" id="h-microplastics-on-the-move">Microplastics on the move</h2>



Laboratory flumes show that buoyant fibers drift through wastewater, rivers, and finally reservoirs that feed municipal plants. 



Filtration and flocculation remove many, yet not all escape: <a href="https://cdn.who.int/media/docs/default-source/wash-documents/microplastics-in-dw-information-sheet190822.pdf" target="_blank" rel="noreferrer noopener">counts</a> ranging from zero to 1,000 particles per quart have been recorded in treated drinking water.



The <a href="https://www.who.int/news/item/20-08-2019-microplastics-in-drinking-water" target="_blank" rel="noreferrer noopener">World Health Organization</a> concluded that present levels “do not pose an immediate threat to human health,” while urging deeper monitoring. Researchers agree the data set is small and detection methods vary, leaving large gaps.



<h2 class="wp-block-heading" id="h-microplastics-and-your-body">Microplastics and your body</h2>



Micro- and nanoplastics have deleterious impacts on mammalian endocrine components such as hypothalamus, thyroid, and ovaries. 



Animal studies connect plastic fragments to hormone disruption, oxidative stress, and altered metabolism. 



Fragments have also been spotted in human tissue. A 2023 <a href="https://pubmed.ncbi.nlm.nih.gov/33395930/" target="_blank" rel="noreferrer noopener">investigation</a> identified polymer specks lodged inside the placenta, demonstrating that particles can cross biological barriers.



Scientists caution that laboratory doses often exceed real‑world exposure. Still, many microplastic fibers carry additives, and their rough surfaces can pick up heavy metals, raising concern over cumulative effects.



<h2 class="wp-block-heading" id="h-sponge-quality-impacts-waste">Sponge quality impacts waste</h2>



Not every brand sheds the same volume. In Ji’s tests, denser foams resisted fracture and produced fewer fibers per stroke than light, airy versions.



Manufacturers could tweak the polymer recipe or add reinforcing binders to slow wear. Durability would keep the scrubbing power while cutting emissions at the source.



Consumers have options while waiting for product redesigns. Natural <a href="https://www.earth.com/news/the-future-of-plastic-biodegradable-durable-and-even-edible/">cellulose</a> or copper scouring pads abrade stains without plastic dust, though they may scratch delicate coatings.



Rotating tools helps one sponge last longer. Allowing the block to dry fully between uses reduces internal swelling, another cause of breakage.



<h2 class="wp-block-heading" id="h-melamine-sponges-and-microplastics">Melamine, sponges, and microplastics</h2>



Household items shed many kinds of debris: polyester laundry, tire dust, and even tea bags contribute to the growing swirl. Tracking each stream reveals both the complexity and the opportunity for targeted fixes.



Small fibers add up because use is constant. The magic‑sponge tally rivals global microfiber discharge from tumble‑dryer vents, reminding us that minor conveniences scale into major outputs.



Scientists still lack a standard way to measure polymer fragments across <a href="https://www.earth.com/news/unidentified-chemical-found-in-tap-water-across-the-u-s/">water</a>, food, and air. Comparing datasets is difficult, so regulators hesitate to set limits.



Future studies will probe how shape and chemistry influence uptake by cells. Ji’s group now tests whether the branched fibers of melamine foam behave differently from threads released by clothing.



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



Municipal water plants can upgrade with finer membranes that cost far less than a full system overhaul, while households can install under-sink carbon block filters to catch many fragments and improve water taste. 



Policymakers, meanwhile, can steer manufacturers toward tougher, low-shedding foams through procurement guidelines for schools and offices - bulk orders that often shape what ends up on store shelves.



Melamine sponges gained popularity for erasing permanent marker without harsh chemicals, but the next challenge is keeping that cleaning power while reducing invisible waste. 



Ji remains optimistic, comparing abrasion control to seat-belt adoption - a quiet fix that evolved into a daily safeguard.



The study is published in <a href="https://pubs.acs.org/doi/10.1021/acs.est.4c00846" target="_blank" rel="noreferrer noopener">Environmental Science &amp; Technology</a>.



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Scientists warn that your favorite sponge could be contaminating the water you drink

A faded coffee ring on a countertop can vanish with...

Hidden inside the chests of nearly 700 Toronto residents, doctors have spotted the faint fingerprints of air pollution.



Using one of medicine’s most sensitive tools - cardiac magnetic resonance imaging - researchers have shown that long-term exposure to fine particulate matter, or PM2.5, is linked to subtle scarring of the heart muscle, known as diffuse myocardial fibrosis.



The finding helps explain why people who live with polluted air face a greater risk of heart failure, heart attacks, and other <a href="https://www.earth.com/news/heart-disease-patients-have-a-unique-vulnerability-to-air-pollution/">cardiovascular problems</a>.



<h2 class="wp-block-heading" id="h-tiny-pollutant-big-damage">Tiny pollutant, big damage</h2>



PM2.5 refers to particles less than 2.5 micrometers in diameter, small enough to bypass the lungs’ natural filtering defenses and pass directly into the bloodstream.



Traffic exhaust, coal-fired power plants, industrial smokestacks, and even wildfire smoke all contribute to PM2.5 pollution.



While previous studies have repeatedly shown correlations between high PM2.5 levels and cardiovascular disease, the biological chain of events connecting the two remained hazy.



Kate Hanneman, a cardiothoracic radiologist at the <a href="https://www.utoronto.ca/">University of Toronto</a> and the <a href="https://www.uhn.ca/">University Health Network</a>, is the senior author of the study.



“If you’re exposed to <a href="https://www.earth.com/news/air-pollution-map-reveals-health-threats-from-tiny-particles/">air pollution</a>, you’re at higher risk of cardiac disease, including having a heart attack,” she said. “We wanted to understand what drives this increased risk at the tissue level.”



<h2 class="wp-block-heading" id="h-heart-scans-uncover-pollution-s-toll">Heart scans uncover pollution’s toll</h2>



Hanneman’s team recruited 201 healthy volunteers and 493 patients diagnosed with dilated cardiomyopathy, a condition that weakens the heart’s pumping ability.



Each participant underwent a sophisticated MRI scan that measures how strongly the <a href="https://www.earth.com/news/heart-muscles-may-soon-be-able-to-regenerate-like-other-muscles/">heart muscle</a> holds onto a contrast dye. From that signal, physicians can calculate the degree of microscopic scarring that standard tests would otherwise miss.



The researchers then used satellite data, government air-quality monitors, and residential histories to estimate a decade’s worth of PM2.5 exposure for every participant. 



Even within the relatively modest pollution levels found in Canadian cities, a clear pattern emerged. Higher long-term exposure to PM2.5 was linked with higher levels of myocardial fibrosis. 



Particulate pollution may harm hearts even without pre-existing disease, affecting both cardiomyopathy patients and healthy individuals.



<h2 class="wp-block-heading" id="h-pollution-hits-harder-for-some">Pollution hits harder for some</h2>



A deeper dive into the numbers revealed that some groups bear a disproportionate burden. Women showed a stronger pollution-fibrosis relationship than men. Smokers and people with <a href="https://www.earth.com/news/scientists-identify-minimum-amount-of-physical-activity-needed-to-prevent-high-blood-pressure/">hypertension</a> also displayed heightened sensitivity. 



Those findings suggest that physiological or lifestyle factors can amplify the heart’s vulnerability to polluted air.



“Even modest increases in air pollution levels appear to have measurable effects on the heart,” Hanneman said.



“Our study suggests that air quality may play a significant role in changes to heart structure, potentially setting the stage for future cardiovascular disease.”



<h2 class="wp-block-heading" id="h-below-the-regulatory-radar"><a></a>Below the regulatory radar</h2>



One of the study’s most striking conclusions is that harmful changes occur well below many national and international air-quality standards. 



Most of the Toronto cohort lived in neighborhoods that meet Canadian and World Health Organization guidelines. Yet the researchers still saw progressive scarring as pollution levels rose incrementally.



Public health policy often hinges on the idea of a safe threshold, but these results challenge that assumption.



“There have been improvements in <a href="https://www.earth.com/news/wildfires-are-changing-the-quality-of-our-air/">air quality</a> over the past decade, both in Canada and the United States, but we still have a long way to go,” Hanneman said.



She argues for more stringent regulations, better monitoring, and meaningful reductions in emissions from transportation, industry, and wildfire-prone landscapes.



<h2 class="wp-block-heading" id="h-pollution-seen-through-mri">Pollution seen through MRI</h2>



The work also expands the role of medical imaging beyond traditional diagnostics. “Medical imaging can be used as a tool to understand environmental effects on a patient’s health,” Hanneman explained.



By identifying and quantifying early tissue changes caused by pollution, imaging specialists can collaborate with cardiologists, epidemiologists, and public health officials to refine risk prediction and guide interventions.



For clinicians, the practical takeaway is that environmental history belongs in the exam room. 



If a patient commutes along congested highways, works at an industrial facility, or lives downwind of frequent <a href="https://www.earth.com/news/climate-change-is-making-wildfire-smoke-more-deadly/">wildfires</a>, physicians may want to factor that exposure into cardiovascular risk assessments. 



These environmental risks could be considered alongside established factors like smoking or hypertension.



<h2 class="wp-block-heading" id="h-tracking-long-term-heart-damage">Tracking long-term heart damage</h2>



The Toronto team plans to follow its volunteers over time to see whether diffuse fibrosis translates into overt heart disease and whether reducing pollution exposure can halt or reverse the damage. 



The experts also hope to replicate the study in regions with higher PM2.5 levels to test whether the relationship strengthens under harsher conditions.



Meanwhile, policymakers can draw a clear lesson: cutting particulate pollution yields not only cleaner skies but healthier hearts. Every gram of soot kept out of the atmosphere is a gram of microscopic scarring averted in the population’s cardiac muscle.



The study is published in the journal <a href="https://pubs.rsna.org/doi/10.1148/radiol.250331">Radiology</a>.



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Air pollution may quietly scar your heart

Hidden inside the chests of nearly 700 Toronto residents, doctors...

If you’ve ever blamed a slice of pizza or a bowl of ice cream for a restless night of sleep, you’re not alone - and you might be onto something. 



A new survey of more than 1,000 Canadian college students links certain food sensitivities, especially lactose intolerance, to poorer sleep and a spike in unsettling dreams.



“Nightmare severity is robustly associated with lactose intolerance and other food allergies,” said lead author Tore Nielsen from the <a href="https://www.umontreal.ca/en/">University of Montréal</a>. 



“These new findings imply that changing eating habits for people with some food sensitivities could alleviate <a href="https://www.earth.com/news/nightmares-daymares-hallucinations-may-be-early-warning-signs-serious-disease/">nightmares</a>.”



<h2 class="wp-block-heading" id="h-tracking-diet-and-dreams">Tracking diet and dreams</h2>



Folk wisdom has long insisted that a heavy meal - or the wrong one - can wreck a good night’s rest. But solid data has been thin.



To dig deeper, Nielsen’s team surveyed 1,082 students at <a href="https://www.macewan.ca/home/">MacEwan University</a> in Edmonton. They asked about eating, bedtime and wake-up routines, overall <a href="https://www.earth.com/news/sleep-quality-could-be-the-key-to-better-metabolic-health/">sleep quality</a>, dream recall, and how often respondents suffered nightmares. 



Next, the researchers zeroed in on eating patterns, known food allergies or intolerances, and any personal hunch that certain foods affect dreams.



Roughly one-third of participants reported frequent nightmares. Women were more likely than men to remember their dreams and to say they slept poorly. They also reported food intolerances almost twice as often.



About 40 percent of all students felt that late-night eating or specific ingredients influenced their sleep, while roughly 25 percent believed certain foods made their nights specifically worse.



<h2 class="wp-block-heading" id="h-dairy-blamed-for-sleep-loss">Dairy blamed for sleep loss</h2>



Among those who pinned their sleep woes on food, sweets, spicy dishes, and dairy products topped the list of potential villains. 



Yet the most consistent pattern emerged when researchers compared diagnosed food sensitivities to nightmare frequency. 



Students who were lactose intolerant had more gastrointestinal discomfort at night, recalled more nightmares, and rated their sleep quality as poorer.



“Nightmares are worse for lactose-intolerant people who suffer severe gastrointestinal symptoms and whose sleep is disrupted,” Nielsen noted. “This makes sense, because we know that other bodily sensations can affect dreaming.”



The logic is straightforward. If undigested lactose creates gas and cramping, that discomfort can seep into the dreaming brain, morphing into threatening imagery and prompting abrupt awakenings.



Repeated interruptions prevent sleepers from cycling into the deeper, restorative stages of rest - and can reinforce a vicious loop of dread and disturbed sleep.



<h2 class="wp-block-heading" id="h-distress-signals-in-the-brain">Distress signals in the brain</h2>



Only about 5 percent of students believed specific <a href="https://www.earth.com/news/eating-more-fruits-and-vegetables-will-help-you-get-better-sleep/">foods</a> colored the tone of their dreams, but those few often put the blame on dairy or sugary treats.



Interestingly, a similar survey Nielsen ran 11 years ago found a larger share of students convinced that food shapes dreams. 



The drop-off might reflect growing public awareness of food allergies. For example, people who know milk upsets their stomachs may simply avoid it at night, dulling any obvious link.



Still, the new results echo a broader scientific push to understand the “gut-brain axis,” the two-way communication network that lets digestive distress influence mood, cognition, and, apparently, dreamscapes. 



Even modest belly rumblings can send distress signals northward, nudging the brain to script darker stories.



<h2 class="wp-block-heading" id="h-can-food-really-shape-dreams">Can food really shape dreams?</h2>



Of course, correlation doesn’t prove cause. People who eat poorly may sleep poorly - but chronic sleep loss can also drive cravings for comfort foods. Stress, <a href="https://www.earth.com/news/resistance-exercise-in-the-evening-can-improve-sleep/">exercise</a>, and genetics muddy the waters further.



Nielsen calls for controlled trials: volunteers would eat dairy or placebo snacks before bed while researchers monitor gut activity, brain waves, and dream reports.



“We are routinely asked whether food affects dreaming - especially by journalists on food-centric holidays,” Nielsen said. “Now we have some answers.”



Yet big questions linger. Do other intolerances, like gluten sensitivity, twist dream content? Are the effects different in older adults or in kids? And how does mental health, which can influence both diet and dreaming, intertwine with these findings?



<h2 class="wp-block-heading" id="h-eat-early-to-stop-nightmares">Eat early to stop nightmares</h2>



While science sorts out the details, the advice is common-sense: if you know milk or cheese bothers you, avoid it late in the evening, especially if nightmares plague you. 



For anyone prone to indigestion at bedtime, lighter, earlier dinners and a pause on sugary or spicy snacks can’t hurt.



More broadly, the study nudges sleep hygiene beyond blue-light screens and blackout curtains to include what (and when) we eat. Our digestive tract doesn’t clock out at night; its complaints can echo loudly in the dream theater.



Until researchers run those carefully controlled cheese-before-bed experiments, moderation in the kitchen remains the gentlest path to sweeter dreams - and quieter nights.



The study is published in the journal <a href="https://www.frontiersin.org/journals/psychology/articles/10.3389/fpsyg.2025.1544475/full">Frontiers in Psychology</a>.



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Nightmares could be triggered by what you eat

If you’ve ever blamed a slice of pizza or a...

Carbon dioxide usually takes center stage in climate talks, yet it is not the only culprit turning up Earth’s thermostat. A group of heat‑trapping compounds known as super pollutants packs an outsized punch, both for the atmosphere and for our lungs.



Unlike carbon dioxide, these <a href="https://www.earth.com/news/world-environment-day-2025-plastic-pollution-is-choking-our-planet/">pollutants</a> linger for only days to a few years, so cleaning them up can cool the planet and clear the air within a single political term.



Drew Shindell, a climate scientist at <a href="http://Duke University https://g.co/kgs/4dGmi2p">Duke University</a> and long‑time contributor to the Intergovernmental Panel on Climate Change (<a href="https://www.ipcc.ch/">IPCC</a>), refers to the group as “low‑hanging fruit for a safer future.”



<h2 class="wp-block-heading" id="h-cutting-super-pollutants-now">Cutting super pollutants now </h2>



Super <a href="https://www.earth.com/news/earth-day-2025-our-power-our-planet/">pollutants</a> are responsible for almost half of the warming recorded since the industrial era began, according to a 2018 briefing from the <a href="https://www.ccacoalition.org/sites/default/files/resources/2018_infosheet_slcps_ccac.pdf" target="_blank" rel="noreferrer noopener">Climate and Clean Air Coalition</a>. Cutting them now buys precious time while nations decarbonize their power grids.



Because they fade quickly, the temperature response is just as quick. A strong push on <a href="https://www.epa.gov/gmi/importance-methane" target="_blank" rel="noreferrer noopener">methane</a> alone could avoid about 0.5 °F (0.28 °C) of warming by the 2040s, the <a href="https://www.igsd.org/wp-content/uploads/2024/01/IGSD-Methane-Primer.pdf" target="_blank" rel="noreferrer noopener">Institute for Governance &amp; Sustainable Development</a> estimated.



<h2 class="wp-block-heading" id="h-biggest-super-pollutant-sources">Biggest super pollutant sources</h2>



Methane has 86 times the <a href="https://www.earth.com/news/dust-storms-are-a-surprising-source-of-deadly-air-pollution/">warming</a> power of carbon dioxide during its first twenty years aloft, the press release noted. It leaks from oil and gas fields, escapes landfills, and bubbles out of rice paddies.



<a href="https://www.ccacoalition.org/short-lived-climate-pollutants/black-carbon" target="_blank" rel="noreferrer noopener">Black carbon</a>, the sooty particle that darkens smoke plumes, hangs around for barely two weeks yet warms 1,500 times more per ton than carbon dioxide. Road traffic, wood stoves, and wildfires are the leading sources.



Tropospheric ozone is not emitted directly. Sunlight cooks methane, nitrogen oxides, and volatile organic compounds to create this lung‑irritating gas, which persists for only days but still drives warming.



<a href="https://www.ccacoalition.org/short-lived-climate-pollutants/hydrofluorocarbons-hfcs" target="_blank" rel="noreferrer noopener">Hydrofluorocarbons</a> keep refrigerators cold and office buildings comfortable, while <a href="https://my.clevelandclinic.org/health/treatments/nitrous-oxide-laughing-gas" target="_blank" rel="noreferrer noopener">nitrous oxide</a> rises from fertilizer. Both belong to the super pollutant club even though they have far lower direct health impacts.



<h2 class="wp-block-heading" id="h-how-super-pollutants-harm-health">How super pollutants harm health</h2>



Soot and ground‑level ozone are part of the air pollution mix that claims 6.7 million lives every year, the <a href="https://www.who.int/teams/environment-climate-change-and-health/air-quality-and-health/health-impacts/types-of-pollutants" target="_blank" rel="noreferrer noopener">World Health Organization</a> estimates. Ozone alone accounts for roughly 2.4 million of those deaths through heart and lung disease, the Clean Air Task Force <a href="https://cdn.catf.us/wp-content/uploads/2024/11/19120324/troposheric-report.pdf" target="_blank" rel="noreferrer noopener">reports</a>.



Black carbon’s fine particles penetrate deep into the bloodstream, raising blood pressure, worsening asthma, and affecting fetal growth. Scientists are still unraveling how toxic the particle is compared with other <a href="https://en.air-q.com/messwerte/feinstaub" target="_blank" rel="noreferrer noopener">PM₂.₅</a> ingredients.



<h2 class="wp-block-heading" id="h-linking-health-and-climate">Linking health and climate</h2>



While climate change and public health are deeply linked, many experts still treat them as separate issues. This disconnect has slowed coordinated responses to super <a href="https://www.earth.com/news/air-pollution-can-reshape-a-babys-brain-before-birth/">pollutants</a>, especially when the pollutant isn't immediately toxic to breathe.



For example, methane doesn't directly harm human lungs, so it's often left out of air quality policies. But methane is a major precursor to tropospheric ozone, which is deadly in polluted cities and rural areas alike.



<h2 class="wp-block-heading" id="h-pollution-hurts-food-and-water">Pollution hurts food and water</h2>



Ozone sneaks into plant tissue and slashes crop yields. Global models suggest up to twelve percent of staple grains are lost each year because of methane‑driven ozone formation that threatens food supplies in already vulnerable regions, the <a href="https://www.ccacoalition.org/sites/default/files/resources/2021_Global-Methane_Assessment_full_0.pdf" target="_blank" rel="noreferrer noopener">CCAC briefing</a> adds.



Soot, meanwhile, dims sunlight and shifts rainfall. When it settles on mountain snow, the dark dust speeds up melting, thereby disrupting drinking‑water supplies far downstream.



<h2 class="wp-block-heading" id="h-fast-ways-to-cool-the-planet">Fast ways to cool the planet</h2>



An old <a href="https://www.science.org/doi/10.1126/science.1210026" target="_blank" rel="noreferrer noopener">analysis</a> led by Shindell identified 14 ready‑to‑deploy measures, ranging from sealing gas wells to filtering diesel exhaust, that could trim expected warming in 2050 by about 0.9 °F (0.5 °C) while preventing millions of premature deaths.



The same package would save agricultural crops worth tens of billions of dollars every year, showing that climate, health, and economic gains often march together.



<h2 class="wp-block-heading" id="h-cutting-super-pollutants-effectively">Cutting super pollutants effectively</h2>



Oil and gas firms can spot methane plumes with infrared cameras and satellites, then patch leaks at low cost. Cattle feed additives cut <a href="https://science.nasa.gov/climate-change/faq/which-is-a-bigger-methane-source-cow-belching-or-cow-flatulence/" target="_blank" rel="noreferrer noopener">bovine methane belches</a> by as much as 30 percent.



Households can replace smoky wood stoves with electric induction cooktops. Cities that restrict high‑emitting vehicles show immediate drops in black carbon, making bus stops and playgrounds safer for children.



<h2 class="wp-block-heading" id="h-local-action-to-global-pledges">Local action to global pledges</h2>



More than 100 countries have signed the <a href="https://www.globalmethanepledge.org/" target="_blank" rel="noreferrer noopener">Global Methane Pledge</a>, committing to a 30 percent cut by 2030. Meeting the goal could avert 690,000 premature deaths a year by mid‑century, according to <a href="https://www.nature.com/articles/s41612-022-00247-5" target="_blank" rel="noreferrer noopener">models</a>.



Regulators can also fold super pollutants into national climate plans under the Paris agreement, ensuring that air‑quality and greenhouse‑gas rules pull in the same direction.



<h2 class="wp-block-heading" id="h-achieving-global-climate-goals">Achieving global climate goals</h2>



Scientists still need better monitoring. Low‑cost sensors on school rooftops, paired with satellite data, are beginning to map pollution hot spots in real time.



“To achieve global climate goals, we must reduce methane emissions while also urgently reducing carbon dioxide emissions,” said Shindell during a United Nations press briefing on the <a href="https://www.unep.org/news-and-stories/press-release/global-assessment-urgent-steps-must-be-taken-reduce-methane" target="_blank" rel="noreferrer noopener">Global Methane Assessment</a>.



Faster progress hinges on funding such dual‑benefit projects.



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Cutting super pollutants could quickly cool the planet

Carbon dioxide usually takes center stage in climate talks, yet...

Once native to the rocky shores of Jeju Island, the top shell Turbo sazae is now moving north. Scientists at KIOST have linked the snail's shifting range to rising sea temperatures driven by climate change.



Genetic evidence supports the snails' expansion, showing shared ancestry between eastern and southern Korean populations.



A research paper published in the journal Animals reveals that this shift is not just recent. It is tied to deeper evolutionary history and ocean current dynamics.



“<a href="https://www.earth.com/news/climate-wins-in-2025-came-from-unexpected-places/">Climate</a> change-driven rises in sea temperatures are a core variable in the impact of climate change on marine ecosystems,” said <a href="https://www.kiost.ac.kr/eng.do" target="_blank" rel="noreferrer noopener">KIOST</a> President Hyi Seung Lee.



<h2 class="wp-block-heading" id="h-snails-with-shared-ancestry">Snails with shared ancestry</h2>



The researchers collected samples from six locations, including Jeju and the East Sea. Using mitochondrial DNA (COI), the team built haplotype maps to assess relatedness. 



A dominant genetic type, called EJ1, appeared in 60% of Jeju individuals and 50% of East Sea ones. This strong overlap suggests these <a href="https://www.earth.com/news/climate-change-is-now-impacting-earths-rotation/">regions</a> share more than just warm waters. They share a common genetic base. 



Bayesian analysis dated the most recent common ancestor between these populations to between 9.7 and 23.3 million years ago. 



<h2 class="wp-block-heading" id="h-ocean-currents-and-snail-dispersal">Ocean currents and snail dispersal</h2>



The ancestral link between the snails reflects a long evolutionary history shaped by currents like the Kuroshio and Tsushima. 



These ocean currents are central to the story. They carry larvae north during early planktonic stages. Turbo sazae larvae live in open water for 3 to 5 days before settling. That short window is enough to disperse widely along current paths.



This dispersal helps maintain genetic continuity between distant populations. That is why genetic differentiation between Jeju and the East Sea is low. 



The study’s FST values and AMOVA results confirm that most genetic variation occurs within, not between, these groups.



<h2 class="wp-block-heading" id="h-unique-regions-still-shape-genes">Unique regions still shape genes</h2>



Despite shared ancestry, some sites showed early signs of divergence. Populations at Dokdo and Wangdolcho had site-specific haplotypes. 



These locations have complex underwater topography and eddies that may trap larvae. This can limit outside gene flow and shape unique <a href="https://www.earth.com/news/earth-is-just-three-years-away-from-dangerous-carbon-milestone/">traits</a> over time.



Dokdo, for instance, rises steeply from the ocean floor and is shaped by dynamic currents. These geographic features might create local barriers that influence how genes move. More research could clarify whether such structures truly restrict connectivity.



<h2 class="wp-block-heading" id="h-warmer-waters-weaken-snail-immunity">Warmer waters weaken snail immunity</h2>



Earlier studies suspected diet changes caused population drops in Jeju. Researchers thought urchin barrens affected feeding behavior. But recent findings show diet had little impact on physiology or reproduction. 



Instead, warming waters weakened the snail’s immune function. In other words, climate change was the real driver of the snail's population decline around Jeju.



This finding came from a second study published in the journal Marine Environmental Research. The study confirmed that higher sea temperatures compromise the snail’s immunity and make it more vulnerable to environmental stress.



<h2 class="wp-block-heading" id="h-ocean-warming-shifts-sea-life-habitats">Ocean warming shifts sea life habitats</h2>



Between 2009 and 2018, Turbo sazae expanded north at a rate of 12.4 km per year. That is a fast pace for a marine mollusk. It aligns with rising sea surface temperatures of 0.38°C per decade in the region. Warmer waters now support life where it once could not.



A marine desertification phenomenon called barren ground is also changing <a href="https://www.earth.com/news/climate-change-is-fueling-antibiotic-resistance-in-our-soils/">habitats</a>. These zones lose kelp and become covered with white algae. Such shifts leave snails like T. sazae with fewer choices. They must move or decline.



<h2 class="wp-block-heading" id="h-climate-change-and-snail-conservation">Climate change and snail conservation </h2>



The study's findings have practical implications. They show that Jeju acts as a source for new East Sea populations. 



The shared genetics suggest that populations should not be managed as isolated units. Instead, integrated approaches should reflect their connectivity.



Yet, local differences still matter. Management plans must protect unique habitats, especially where signs of early genetic differentiation emerge. Monitoring, habitat conservation, and tracking larval dispersal are essential steps.



<h2 class="wp-block-heading" id="h-snails-adjusting-to-climate-change">Snails adjusting to climate change </h2>



As the sea changes with the climate, snails and other inhabitants are changing too. Turbo sazae is adjusting, relocating, and surviving. 



The science behind this shift not only charts the path of one species. It gives a broader glimpse into how ocean warming is reshaping sea life. 



KIOST President Hyi Seung Lee said the findings will help deepen scientific understanding of how sea life distribution is changing and support ongoing efforts to protect marine ecosystems.



The study is published in the journal <a href="https://www.mdpi.com/2076-2615/15/9/1321" target="_blank" rel="noreferrer noopener">Animals</a>.



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Ocean warming is pushing sea life into new territories

Once native to the rocky shores of Jeju Island, the...

Many adults trust AI systems that confidently give wrong answers. Children, who lack deep domain knowledge, often find it even harder to tell when AI is wrong. 



A new game developed by <a href="https://www.washington.edu" target="_blank" rel="noreferrer noopener">University of Washington</a> researchers flips the script. It helps kids recognize AI’s failures and think more critically about its logic.



<h2 class="wp-block-heading" id="h-kids-test-ai-logic">Kids test AI logic</h2>



AI Puzzlers draws its design from the Abstraction and Reasoning Corpus (ARC), a set of visual puzzles that are easy for humans and hard for <a href="https://www.earth.com/news/new-ai-framework-dimon-turning-any-laptop-into-a-supercomputer/">machines</a>. These puzzles don’t require language. Instead, they ask users to spot a pattern and apply it to new inputs using color grids.



The game engages kids by asking them to solve puzzles first. Then, they test <a href="https://www.earth.com/news/ai-model-esm3-creates-new-protein-that-simulates-500-million-years-of-biological-evolution/">AI</a> chatbots on the same puzzles and compare answers. 



Even if the AI sometimes guesses the right answer, its explanation rarely matches. This mismatch becomes a key moment of discovery. Kids learn that confidence doesn’t equal correctness.



“Kids naturally loved ARC puzzles and they’re not specific to any language or culture,” said study lead author Aayushi Dangol. “Because the puzzles rely solely on visual pattern recognition, even kids that can’t read yet can play and learn.”



<h2 class="wp-block-heading" id="h-kids-notice-when-ai-fails">Kids notice when AI fails</h2>



Kids begin by thinking AI is smart. They expect it to outperform them. But when <a href="https://www.earth.com/news/ai-traffic-cameras-are-preventing-thousands-of-crashes-each-year/">AI</a> repeatedly fails, the surprise sparks curiosity and laughter. “That is very very wrong,” one child said after watching an AI completely miss a basic pattern.



Visual comparison helps kids instantly spot what the AI missed. This strengthens their own logic and boosts confidence. They begin to understand that being human brings advantages. Unlike AI, they can use creativity, context, and reasoning grounded in real experience.



One child described the AI as having “the internet’s mind,” saying, “It’s trying to solve it based only on the internet, but the human brain is creative.”



<h2 class="wp-block-heading" id="h-kids-guide-ai-with-better-instructions">Kids guide AI with better instructions</h2>



AI Puzzlers includes a special Assist Mode where kids give the AI clues. This mode turns them into guides, not just players. 



The children move from broad statements like “Make a donut” to specific instructions like “Place white in the center, blue all around.” As they experiment, they learn how to help the AI get closer to the correct logic.



The researchers found that this step-by-step refining deepened the kids’ understanding. They weren’t just pointing out errors. They were learning how <a href="https://www.earth.com/news/video-games-could-accelerate-discoveries-in-cancer-research/">AI</a> misinterprets vague language and how precise input shapes better output.



In one session, a child wrote, “Make a pattern of the colors and gray alternating and a background of white, red, light blue, green, yellow.” The AI still got it wrong. 



The frustration was real. “I am so done with you, AI,” the child said. But the effort showed critical thinking at work.



<h2 class="wp-block-heading" id="h-game-mechanics-that-build-ai-literacy">Game mechanics that build AI literacy</h2>



The game uses three main modes: Manual, AI, and Assist. In Manual Mode, kids build their answers from scratch. 



AI Mode lets them test the chatbot’s performance and read its reasoning. Assist Mode invites them to guide the AI, learning what helps and what doesn’t.



This design is grounded in Mayer and Moreno’s theory of multimedia learning. By using both visuals and text, the game lightens cognitive overload and keeps kids engaged. Switching between modes lets them explore ideas, spot contradictions, and build layered understanding.



<h2 class="wp-block-heading" id="h-kids-can-help-improve-ai">Kids can help improve AI</h2>



The researchers used a participatory design approach called Cooperative Inquiry. In two summer sessions, 21 children aged 6 to 11 collaborated with adult facilitators. These kids weren’t just test subjects. They helped shape the tool.



Children gave feedback, refined features, and even inspired the Assist Mode. In group discussions, they evaluated AI logic, challenged explanations, and brainstormed ideas to improve AI understanding. 



One child noted: “AI is very scientific, given its scientific explanation, but sometimes it’s better not to go super, duper scientific.”



The project showed that children, when given space and tools, are more than passive users. They become critics, testers, and co-creators.



<h2 class="wp-block-heading" id="h-comparing-minds-human-vs-machine">Comparing minds: Human vs. machine</h2>



As they kept solving puzzles, kids saw the difference between how they think and how AI thinks. AI, they noticed, often guesses randomly or repeats errors. 



“AI just keeps guessing,” one child said. Another called it “stupid” and said it only “gets lucky.”



The kids began to frame AI as limited. “Look at the references and think like a human being,” one urged. They recognized that humans can draw from experience, emotion, and logic, while AI relies on patterns it has seen.



This shift is crucial. Children stopped treating AI as infallible. They started viewing it as a tool that needs supervision, not praise.



<h2 class="wp-block-heading" id="h-critical-thinking-in-other-settings">Critical thinking in other settings </h2>



The system is open source and works on any browser. The team hopes to extend it with more puzzle types and newer AI models. They also want to explore if these critical thinking skills transfer to other settings like schoolwork or web searches.



The researchers are also thinking about voice integration and better accessibility for colorblind users. 



The long-term vision is to help kids build habits of questioning, experimenting, and reflecting. These are skills that apply far beyond the game.



<h2 class="wp-block-heading" id="h-puzzles-build-ai-skills">Puzzles build AI skills</h2>



This work shows that critical AI thinking doesn’t need lectures. It can begin with puzzles, color grids, and curiosity. By allowing kids to compare, question, and fix AI logic, AI Puzzlers gives them agency.



“Kids are smart and capable,” said study co-senior author Julie Kientz. “We need to give them opportunities to make up their own minds about what AI is and isn't.”



The success of AI Puzzlers shows what’s possible. When kids are given space to think critically, they don’t just understand AI. They start to outthink it.



The study is published in <a href="https://dl.acm.org/doi/10.1145/3713043.3728836" target="_blank" rel="noreferrer noopener">Proceedings of the 24th Interaction Design and Children</a>.



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Can kids outsmart AI? Puzzle games put them to the test

Many adults trust AI systems that confidently give wrong answers....

Scientists have discovered that microbes in the human gut can absorb PFAS, persistent and toxic chemicals found in our environment. This breakthrough could help reduce the harm these chemicals cause inside our bodies.



<a href="https://www.earth.com/news/bacteria-that-eat-forever-chemicals-discovered-in-contaminated-soil/">PFAS</a> (Perfluoroalkyl and Polyfluoroalkyl Substances) are used in waterproof clothing, food packaging, non-stick pans, and cosmetics. They do not break down easily, which makes them useful but dangerous. Over time, they build up in soil, water, and living organisms, including us.



PFAS exposure has been linked to fertility problems, cancer, immune suppression, and heart disease. Now, research led by the <a href="https://www.cam.ac.uk" target="_blank" rel="noreferrer noopener">University of Cambridge</a> offers a possible solution using our own gut bacteria.



<h2 class="wp-block-heading" id="h-gut-bacteria-remove-toxic-chemicals">Gut bacteria remove toxic chemicals</h2>



The study, published in the journal Nature Microbiology, identified nine gut bacterial strains that can bind and trap PFAS molecules. The researchers introduced these strains into the gut of mice to create a human-like microbiome.



After feeding the mice with <a href="https://www.earth.com/news/bacteria-strain-identified-that-can-eat-forever-chemicals/">PFAS</a>, the team observed that the bacteria absorbed and stored the chemicals. The PFAS-laden bacteria were then excreted in the faeces.



Within minutes of exposure, some bacteria removed up to 74 percent of PFAS present. Even when exposed to higher PFAS levels, the bacteria removed a consistent percentage. This suggests a reliable process that works across different doses.



<h2 class="wp-block-heading" id="h-most-chemicals-absorbed-by-gut-bacteria">Most chemicals absorbed by gut bacteria </h2>



The bacterial strains included species like&nbsp;Enterocloster bolteae&nbsp;and&nbsp;Blautia producta. According to the paper, these bacteria form intracellular PFAS clumps. This clustering appears to protect the bacteria from PFAS toxicity.



A dose-response analysis showed that higher <a href="https://www.earth.com/news/bacteria-strain-identified-that-can-eat-forever-chemicals/">PFAS</a> levels did not overwhelm the microbes. Instead, the same proportion of PFAS was taken up at all concentrations. That consistency is important for therapeutic use.



The authors also used chemical analysis and imaging to confirm that PFAS accumulated inside bacterial cells and not just on their surface.



<h2 class="wp-block-heading" id="h-removing-pfas-with-probiotics">Removing PFAS with probiotics</h2>



The researchers now aim to develop probiotic supplements that increase these chemical-removing bacteria in the human gut.



“Given the scale of the problem of PFAS ‘forever <a href="https://www.earth.com/news/new-filtration-system-removes-forever-chemicals-from-water/">chemicals</a>’, particularly their effects on human health, it’s concerning that so little is being done about removing these from our bodies,” Dr. Kiran Patil explained who is one of the authors.



“We found that certain species of human gut bacteria have a remarkably high capacity to soak up PFAS from their environment at a range of concentrations, and store these in clumps inside their cells.”



“The reality is that PFAS are already in the environment and in our bodies, and we need to try and mitigate their impact on our health now," said study co-author Dr. Indra Roux.



"We haven’t found a way to destroy PFAS, but our findings open the possibility of developing ways to get them out of our bodies where they do the most harm."



<h2 class="wp-block-heading" id="h-rising-concern-and-a-startup-response">Rising concern and a startup response</h2>



There are over 4,700 PFAS compounds. Some leave the body quickly. Others can remain for decades. These longer-chain PFAS are the most concerning as they accumulate in blood, liver, and other tissues.



The UK government launched a parliamentary inquiry in April 2025 to investigate PFAS regulation and health risks.



Dr. Anna Lindell, the study’s lead author, emphasized the urgency of the issue. “We’re all being exposed to PFAS through our water and food - these chemicals are so widespread that they’re in all of us."



“PFAS were once considered safe, but it’s now clear that they’re not. It’s taken a long time for PFAS to become noticed because at low levels they’re not acutely toxic. But they’re like a slow poison.”



Lindell and Patil co-founded Cambiotics with entrepreneur Peter Holme Jensen. The company is working on PFAS-removal probiotics.



<h2 class="wp-block-heading" id="h-reducing-gut-exposure-to-chemicals">Reducing gut exposure to chemicals</h2>



Until probiotics reach the market, researchers recommend simple lifestyle changes. Avoid using PFAS-coated cookware and install a water filter that reduces PFAS.



These steps will not remove the chemicals already in your body. But they can reduce how much more you take in each day.



The new research shows the gut microbiome may offer a powerful method for managing chemical exposure. Microbes could help protect our health in a polluted world.



The study is published in the journal <a href="https://www.nature.com/articles/s41564-025-02032-5" target="_blank" rel="noreferrer noopener">Nature Microbiology</a>.



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Gut bacteria offer new hope against 'forever chemicals'

Scientists have discovered that microbes in the human gut can...

For many years, scientists believed that plants sensed heat using proteins active mostly at night. But recent findings reveal something far more complex. 



A new study led by Professor Meng Chen from the <a href="https://www.ucr.edu" target="_blank" rel="noreferrer noopener">University of California, Riverside</a>, shows that during the day, <a href="https://www.earth.com/news/plant-roots-could-be-key-to-fighting-climate-change/">plants</a> rely on sugar and a combination of thermal signals to detect warmth and adjust their growth.



The research reshapes long-standing views. The results uncover how plants integrate sunlight, sugar, and internal signals to regulate daytime thermomorphogenesis, the growth response triggered by warmth.



<h2 class="wp-block-heading" id="h-plants-sense-heat-differently-by-day">Plants sense heat differently by day</h2>



“Our textbooks say that proteins like phytochrome B and early flowering 3 (ELF3) are the main thermosensors in plants,” Chen said. “But those models are based on nighttime data." 



"We wanted to know what’s happening during the day, when light and temperature are both high because these are the conditions most <a href="https://www.earth.com/news/human-pressure-has-a-hidden-impact-on-plant-diversity/">plants</a> actually experience.”



Previous models focused on phytochrome B (phyB) and ELF3, both of which are responsive at night. But in strong sunlight, phyB becomes constantly activated, shutting down its heat-sensing role. 



The research team tested Arabidopsis plants under a range of temperatures and red-light intensities, including conditions mimicking midday sun.



The paper shows two clear heat responses. One operates between 12 and 21 °C and depends on phyB. The other, active between 21 and 27 °C, does not rely on phyB. This second, sugar-driven response remains active even under intense light.



<h2 class="wp-block-heading" id="h-sugar-helps-plants-detect-daytime-heat">Sugar helps plants detect daytime heat</h2>



The study reveals that sugar is more than just a fuel. It is a heat signal during daylight. “That’s when we realized sugar wasn’t just fueling growth,” Chen said. “It was acting like a signal, telling the plant that it’s warm.”



Under high temperatures, chloroplasts break down stored starch into sucrose. This sugar then stabilizes PIF4, a protein that drives growth. 



Without sugar, PIF4 degrades. With sugar, PIF4 sticks around, so long as another protein, ELF3, also lifts its repressive control.



The&nbsp;study&nbsp;confirms that adding sucrose to mutant <a href="https://www.earth.com/news/scientists-finally-learn-what-makes-plants-roots-grow-faster-and-stronger-autophagy/">plants</a> restores growth, even in darkness. This shows sugar acts independently from light and provides a thermal cue during the day.



<h2 class="wp-block-heading" id="h-plant-growth-needs-both-sugar-and-heat">Plant growth needs both sugar and heat</h2>



“PIF4 needs two things,” Chen explained. “Sugar to stick around, and freedom from repression. Temperature helps provide both.”



This dual system operates like an "AND" gate in electronics. Both sucrose and the release from ELF3 inhibition are required for full thermoresponsive growth. Sucrose promotes PIF4 stability, while high temperature relieves ELF3's suppression.



When either cue is missing, <a href="https://www.earth.com/news/international-day-for-biological-diversity-2025-bonding-with-nature/">plants</a> fail to elongate properly. But when both are present, like sugar and warmth, PIF4 can trigger auxin-related genes that stretch the plant upwards.



<h2 class="wp-block-heading" id="h-protein-blocks-growth-until-it-s-warm">Protein blocks growth until it’s warm</h2>



Interestingly, ELF3 inhibits PIF4 in two ways. It blocks its production and its activity. High temperatures disable ELF3, freeing PIF4 to act. This insight flips older beliefs that ELF3 only worked at night.



The&nbsp;microscopy images and data on page 8&nbsp;reveal that even without ELF3, plants can respond to sugar and still grow taller. But only with both sugar and heat do PIF4 targets like IAA19 and YUC9 become active.



<h2 class="wp-block-heading" id="h-engineering-stronger-crops">Engineering stronger crops</h2>



“This changes how we think about thermosensing in plants,” Chen said. “It’s not just about proteins flipping on or off. It’s about energy, light, sugar, as well.”



Understanding these systems has practical value. As global temperatures rise, crops need to grow reliably. Knowing that starch breakdown and sugar signaling help regulate growth can help scientists design better, more heat-resilient plants.



Researchers also&nbsp;illustrate how the three thermosensors, phyB, ELF3, and chloroplast-sucrose, work together. This multisensor setup allows plants to fine-tune growth, even under extreme conditions.



<h2 class="wp-block-heading" id="h-plants-use-sugar-smartly-to-grow">Plants use sugar smartly to grow </h2>



Plants live silent lives, but their internal machinery buzzes with complex decisions. In the heat of the day, they don't just react, they calculate. 



By using sugars to sense their environment, they respond with a quiet precision that helps them grow exactly when conditions are right. This study doesn't just add to our knowledge. It rewrites it.



The study is published in the journal <a href="https://www.nature.com/articles/s41467-025-60498-7" target="_blank" rel="noreferrer noopener">Nature Communications</a>.



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Plants use sugar in ways we never imagined

For many years, scientists believed that plants sensed heat using...

Rodents don’t usually evolve overnight. Like most species, they change slowly through tiny shifts passed down over thousands or millions of years. But when the world changes fast, like it has in cities over the past century, some animals keep up. 



In fact, some animals even adapt to urbanization in real time. A team of researchers recently spotted signs of that kind of <a href="https://www.earth.com/news/invasive-species-are-driving-rapid-evolution/">rapid evolution</a>. The clues were found in hundreds of skills sitting quietly in drawers at the Field Museum in Chicago.



The skulls weren’t newly collected specimens - they spanned more than a century. And hidden in their measurements were subtle changes that told a bigger story.



By comparing the skulls of eastern chipmunks and eastern meadow voles collected over the past 125 years, scientists at the Field Museum uncovered signs of these animals adjusting to an increasingly <a href="https://www.earth.com/news/ants-can-effectively-adapt-to-urban-environments/">urban environment</a>.



<h2 class="wp-block-heading" id="h-a-time-machine-in-a-museum">A time machine in a museum</h2>



“Museum collections allow you to time travel,” said Stephanie Smith, a mammalogist and XCT laboratory manager at the Field Museum. 



"Instead of being limited to studying specimens collected over the course of one project, or one person’s lifetime, natural history collections allow you to look at things over a more evolutionarily relevant time scale.”



The Field Museum’s mammal collection includes over 245,000 specimens from around the world, but its home city is especially well represented. These Chicago-area animals offer a rare chance to study changes across both time and space - right in the scientists’ backyard.



“We’ve got things that are over 100 years old, and they're in just as good of shape as things that were collected literally this year,” said Smith. “We thought, this is a great resource to exploit.”



<h2 class="wp-block-heading" id="h-comparing-rodents-in-the-city-of-chicago">Comparing rodents in the city of Chicago</h2>



The team focused on two rodent species that still call Chicago home. <a href="https://www.earth.com/news/small-mammals-play-a-vital-role-in-maintaining-forest-health/">Chipmunks</a>, which live above ground and eat a wide range of food, and <a href="https://www.earth.com/news/social-behavior-of-voles-linked-to-oxytocin-levels/">voles</a>, which live underground and mostly stick to plants. The contrast between them was part of the point.



“We chose these two species because they have different biology, and we thought they might be responding differently to the stresses of urbanization,” said Anderson Feijó, assistant curator of mammals at the Field Museum.



Two interns with the Field Museum Women in Science program - Alyssa Stringer and Luna Bian - played a central role in the work. 



<h2 class="wp-block-heading" id="h-rodent-skulls-and-city-adaptations">Rodent skulls and city adaptations</h2>



The researchers measured the skulls of 132 chipmunks and 193 voles. The skulls hold clues about diet, body size, and even sensory abilities.



“From the skulls, we can tell a little bit about how animals are changing in a lot of different, evolutionary relevant ways - how they're dealing with their environment and how they're taking in information,” said Smith.



Stringer and Bian measured basic features of each rodent skull, like overall length and the length of the tooth rows. 



The researchers also used 3D scanning to digitally map 82 chipmunk and 54 vole skulls. This allowed them to compare tiny differences in shape across specimens using a method called geometric morphometrics.



The results revealed small but telling shifts. Chipmunks showed an increase in skull size, but their tooth rows got shorter. 



Voles developed smaller bony structures in their skulls that are tied to hearing. The changes weren’t random - but they also weren’t clearly linked to temperature or climate.



<h2 class="wp-block-heading" id="h-rodents-respond-to-a-louder-bigger-city">Rodents respond to a louder, bigger city</h2>



To dig deeper, the team used satellite data to track how the city grew over time. They looked at building coverage starting in the 1940s and matched those trends to the locations where specimens were collected. 



Older specimens came from areas known to be wild back then - or from downtown areas that were already developed.



“We tried very hard to come up with a way to quantify the spread of urbanization,” said Feijó. “We took advantage of satellite images showing the amount of area covered by buildings, dating back to 1940.”



<h2 class="wp-block-heading" id="h-changes-driven-by-urbanization">Changes driven by urbanization </h2>



<a href="https://www.earth.com/news/urbanization-is-a-threat-to-78-of-the-worlds-bird-species/">Urbanization</a>, not climate, seemed to drive the rodent skull changes. And the way each species adapted may reflect how it lives.



“Over the last century, chipmunks in Chicago have been getting bigger, but their teeth are getting smaller,” said Feijó. “We believe this is probably associated with the kind of food they're eating."



"They're probably eating more human-related food, which makes them bigger, but not necessarily healthier. Meanwhile, their teeth are smaller - we think it's because they're eating less hard food, like the nuts and seeds they would normally eat.”



As for the voles? The parts of their skulls that hold the inner ear - the auditory bullae - have shrunk. “We think this may relate to the city being loud - having these bones be smaller might help dampen excess environmental noise,” said Smith.



<h2 class="wp-block-heading" id="h-a-warning-not-a-win">A warning, not a win</h2>



It might be tempting to see this as a success story - rodents adjusting to city life. But the scientists see it differently. 



The adaptations may help, but they’re not necessarily positive. Smaller teeth and smaller ear bones are symptoms of change, not signs of health.



“These findings clearly show that interfering with the environment has a detectable effect on wildlife,” said Feijó.



“Change is probably happening under your nose, and you don't see it happening unless you use resources like museum collections,” said Smith.



The full study was published in the journal <a href="https://academic.oup.com/icb/advance-article-abstract/doi/10.1093/icb/icaf081/8158706?redirectedFrom=fulltext">Integrative and Comparative Biology</a>.



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Chicago’s rodents are evolving with the city

Rodents don’t usually evolve overnight. Like most species, they change...

A single fertilized egg somehow manages to build skin, brain, and blood cells within a matter of days. But how do those first cells know which body parts to build? How do some cells know to create kidneys while other cells immediately start creating skin? 



Solving that puzzle has kept developmental biologists busy for more than a century, yet many lineage maps still look like unfinished sketches. 



Now an Australian team reports a tracking tool called LoxCode that labels every cell in a mouse embryo with a unique DNA tag and follows its descendants as tissues form. 



“This creates a trackable barcode, allowing us to peer inside this fundamental process with unprecedented detail,” said <a href="https://findaresearcher.wehi.edu.au/weber.ts" target="_blank" rel="noreferrer noopener">Dr. Tom Weber</a> of the <a href="https://www.wehi.edu.au/" target="_blank" rel="noreferrer noopener">Walter and Eliza Hall Institute</a>.



<h2 class="wp-block-heading" id="h-loxcode-tracks-each-cell-from-the-start">LoxCode tracks each cell from the start</h2>



LoxCode relies on the Cre recombinase enzyme to shuffle short DNA cassettes, generating more than 30 billion possible <a href="https://www.nature.com/articles/s41576-023-00624-7" target="_blank" rel="noreferrer noopener">barcodes</a> in a single step. 



Each label is copied faithfully as the embryo grows, so scientists can reconstruct family trees later by simple sequencing.



In pilot tests, the team injected the barcode cassette on day 5.5 of pregnancy, when the <a href="https://www.sciencedirect.com/topics/neuroscience/epiblast" target="_blank" rel="noreferrer noopener">epiblast</a> is still arranging its first germ layers. A week later they recovered fetuses and read the tags in bulk tissue and at single‑cell resolution.



“That tells us fate bias appears far earlier than textbooks suggest,” explained <a href="https://www.wehi.edu.au/researcher/shalin-naik/" target="_blank" rel="noreferrer noopener">Prof. Shalin Naik</a>, a laboratory head at WEHI. Some clones reached every corner of the embryo, while others stuck to ectoderm, blood, or limb buds.&nbsp;



By feeding the barcode data into an agent‑based model, the researchers predicted hidden asymmetries, like left‑versus‑right kidney precursors, and then confirmed them experimentally. 



Such computational cross‑checks strengthen confidence that the tags truly record biology, not sequencing noise.



<h2 class="wp-block-heading" id="h-how-loxcode-writes-billions-of-labels">How LoxCode writes billions of labels</h2>



Earlier <a href="https://www.science.org/doi/10.1126/science.aaf7907" target="_blank" rel="noreferrer noopener">lineage tracing</a> systems depended on viruses or CRISPR cuts, which can damage cells or miss subtle branches. One <a href="https://www.nature.com/articles/s41586-022-04994-6" target="_blank" rel="noreferrer noopener">CRISPR</a> recorder captured only a few hundred unique edits across a whole zebrafish, limiting resolution.



LoxCode gets around previous limitations by using 13 short pieces of DNA, arranged so that an enzyme called <a href="https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/cre-recombinase" target="_blank" rel="noreferrer noopener">Cre recombinase</a> can shuffle them in many different ways. Once the pieces reach a smaller, stable size, the shuffling stops, locking the DNA tag in place for each cell.



Since each DNA piece is very short, these tags are easy to read using standard genetic sequencing tools. That makes the method affordable, even for labs without large budgets.



The team also created a special breed of mouse, called strain 037677, which is available from <a href="https://www.jax.org/" target="_blank" rel="noreferrer noopener">The Jackson Laboratory</a>. Researchers can use it by pairing it with another mouse that activates the barcoding process in specific tissues.



<h2 class="wp-block-heading" id="h-revealing-hidden-bias-in-the-embryo">Revealing hidden bias in the embryo</h2>



<a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC4699068/" target="_blank" rel="noreferrer noopener">Pluripotent cells</a> were long assumed to wait for external signals before picking a destiny. Yet the new data show many clones already lean toward one germ layer while the fetus is still the size of a poppy seed.



For instance, epiblast cells sitting near the forming early streak produced mostly blood and mesenchyme cells, matching earlier dye‑label <a href="https://www.nature.com/articles/nbt.4103" target="_blank" rel="noreferrer noopener">studies</a> but adding single‑cell resolution.



Conversely, anterior clones favored neural tissues, hinting that position cues translate into lineage bias before gastrulation starts.



Unexpected asymmetries emerged too. The left limb bud often traced back to different founders than the right, suggesting randomness, not mirror symmetry, seeds the first skeletal blueprint.



Such insights could clarify why some <a href="https://www.earth.com/news/cellular-cleanup-helps-preserve-eggs-and-fertility/">congenital disorders</a> strike only one side of the body. LoxCode also gives stem‑cell engineers reference maps for guiding organoids toward balanced growth.



<h2 class="wp-block-heading" id="h-from-brain-growth-to-stroke-repair">From brain growth to stroke repair</h2>



Because barcoding works in live mice, investigators are already adapting it to study immune development, gut regeneration, and tumor relapse. 



A neuroscientist at the <a href="https://www.uq.edu.au/" target="_blank" rel="noreferrer noopener">University of Queensland</a> is tracing how newborn neurons integrate into adult circuits after a stroke, using LoxCode to mark progenitors at the injury edge.



Cancer biologists plan to follow how therapy‑resistant clones emerge over months of drug exposure. By back‑tracking each surviving cell to its earliest barcode, they hope to spot vulnerabilities before relapse.



Drug developers could one day screen compounds that push harmful lineages back toward healthy fates. That approach pairs naturally with <a href="https://www.earth.com/news/rna-breakthrough-sheds-light-on-the-beginning-of-life/">single‑cell RNA</a> profiles, revealing not just where a clone goes but how its gene programs shift along the journey.



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



Developmental disorders often arise from mis‑timed cell decisions that happen weeks before clinical symptoms. 



With a cellular ancestry chart in hand, researchers can pinpoint the first wrong turn and design precise interventions.



<a href="https://www.earth.com/news/vitamin-c-promotes-skin-renewal-and-anti-aging-at-the-genetic-level-dna-demethylation/">Gene therapies</a> that swap faulty DNA in founder cells might correct an entire lineage instead of treating tissues piecemeal. 



Similarly, transplant doctors could verify that lab‑grown grafts contain the right mixture of cell types before surgery.



Ethical questions will follow, especially if human embryos are ever tagged at comparable depth. For now, the focus stays on mice, where LoxCode already promises to rewrite textbooks on early embryonic patterning.



The study is published in the journal <a href="https://linkinghub.elsevier.com/retrieve/pii/S0092867425004611" target="_blank" rel="noreferrer noopener">Cell</a>.



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How do your cells know which parts of your body to build? Brilliant new tech is helping us find out

A single fertilized egg somehow manages to build skin, brain,...

Bird feeding is a cherished pastime across many cultures. Whether it’s scattering breadcrumbs near a city pond or hanging feeders outside suburban windows, millions of people engage in acts of casual care for wild birds. 



Recent research from the <a href="https://www.uark.edu" target="_blank" rel="noreferrer noopener">University of Arkansas</a> reveals that what we feed birds can deeply affect how they handle disease.



The study revealed that canaries on high-protein diets developed stronger immune profiles and milder symptoms when infected with Mycoplasma gallisepticum (MG), a pathogen common in wild <a href="https://www.earth.com/news/hundreds-of-bird-species-could-vanish-in-the-next-century/">songbirds</a>.



“Our results are exciting because of the importance of human supplemented food in wildlife disease systems, especially wild birds, which are commonly provided with supplemental food via bird feeders,” said Erin Sauer, lead author of the study.



This research is the first to link diet with molecular-level immune differences in wildlife. It focuses on how food type - not just quantity - shapes disease outcomes in birds.



<h2 class="wp-block-heading" id="h-protein-fed-birds-recover-faster">Protein-fed birds recover faster</h2>



The researchers divided canaries into two groups. One group received a high-protein diet made mostly of egg whites, while the other received a high-fat diet with more yolk and oil. Birds were then exposed to the MG pathogen or given a harmless placebo.



Before infection, protein-fed <a href="https://www.earth.com/news/bird-evolution-timeline-pushed-back-20-million-years-by-baminornis-zhenghensis-discovery/">birds</a> already showed increased expression of immune-related genes. After infection, lipid-fed birds had to ramp up their immune systems, while protein-fed birds maintained steady, high-level expression. This shows their immune systems were already ready.



Protein-fed birds recovered faster. Their eye inflammation - a symptom of MG - was lower and cleared quicker. Lipid-fed birds took longer to recover, with more prolonged symptoms.



<h2 class="wp-block-heading" id="h-immune-gene-activity-before-infection">Immune gene activity before infection</h2>



The team used RNA sequencing to analyze gene activity. Before infection, protein-fed <a href="https://www.earth.com/news/birds-are-struggling-to-keep-pace-with-a-warming-climate/">birds</a> had 267 genes upregulated related to immune defense. 



Lipid-fed birds had 248 different genes upregulated, many tied to basic cellular functions like ribosome activity, not immunity.



After infection, the contrast grew. Lipid-fed birds showed over 1,000 genes with significant changes. Protein-fed birds had only 66 such genes. 



This means lipid-fed birds had to drastically adjust their systems during infection. Protein-fed birds needed little change - they were already prepared.



Surprisingly, immune genes like JCHAIN (linked to antibody production) were seven times more active in protein-fed birds before infection. Lipid-fed birds only caught up after infection, suggesting delayed immune readiness.



<h2 class="wp-block-heading" id="h-metabolic-clues-and-broader-implications">Metabolic clues and broader implications</h2>



Diet also influenced energy-related genes. Lipid-fed birds showed signs of stress in genes tied to mitochondrial function and insulin regulation. 



One gene, LEPR (leptin receptor), responded in opposite ways between the two groups. This points to broader metabolic differences that could influence disease tolerance.



These molecular effects mirror patterns seen in wild house finches that have evolved tolerance to MG. This suggests that simple dietary changes can mimic the effects of natural selection.



<h2 class="wp-block-heading" id="h-what-backyard-bird-lovers-can-do">What backyard bird lovers can do</h2>



So what can people feeding backyard <a href="https://www.earth.com/news/birds-may-be-using-quantum-physics-for-migration/">birds</a> take from this study?



Sauer suggests giving birds high-protein and nutrient-dense options. These include suet with seeds, mealworms, peanuts, and sunflower seeds. These foods support birds’ immune systems and overall condition.



Avoid feeding mostly cracked corn, millet, or bread. These offer limited nutritional value. Still, birds may need more fat during winter or migration, so balance matters. Birds will often choose what they need most.



<h2 class="wp-block-heading" id="h-protein-can-boost-birds-survival">Protein can boost birds' survival</h2>



This study shows that everyday actions, like feeding birds, can directly impact their survival and overall health. While feeding may seem harmless or routine, the type of food offered plays a critical role. 



Poor-quality food can weaken birds' immune systems, making them less able to fight infections and recover from illness.



As human activity continues to reshape natural landscapes and spread disease more widely, our role in supporting wildlife becomes even more important. 



The research reminds us that meaningful change often begins with small, consistent habits. Offering nutrient-rich, protein-balanced food helps birds stay strong, boost immunity, and recover faster when sick or stressed.



Even simple choices at backyard feeders, such as selecting better ingredients, can strengthen birds’ natural defenses. These actions become a powerful way to support bird populations. 



The study is published in the journal <a href="https://onlinelibrary.wiley.com/doi/10.1111/mec.17793" target="_blank" rel="noreferrer noopener">Molecular Ecology</a>.



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Protein helps birds prepare to fight off infection

Bird feeding is a cherished pastime across many cultures. Whether...

Giant,Male,Cuttlefish,With,Stripe,Tentacles

When we imagine the ancient oceans, we often picture massive reptiles and shelled ammonites dominating the waters. For decades, paleontologists believed these creatures ruled the Mesozoic Era without much competition. 



However, a new study from Hokkaido University&nbsp;challenges that idea by revealing the unexpected dominance of <a href="https://www.earth.com/news/how-squid-power-their-amazing-camouflage-abilities/">ancient</a> squids.



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



Squids are remarkable marine invertebrates belonging to the class <a href="https://www.earth.com/news/octopus-and-squid-senses-linked-to-human-brain-evolution/">Cephalopoda</a>, which they share with octopuses and cuttlefish. Their biology showcases some of nature’s most fascinating adaptations. 



Squids possess a mantle cavity for jet propulsion, using rapid water expulsion to move with precision and speed. Their large, complex eyes rival those of vertebrates, providing excellent vision crucial for detecting predators and prey in the dimly lit depths. 



Internally, they have a beak-like jaw and a radula for processing food, typically fish and crustaceans. One of their most iconic features is their ability to release ink, a defense mechanism that creates a smokescreen, enabling a quick escape.



Behaviorally, squids exhibit <a href="https://www.earth.com/news/scientists-unlock-the-light-bending-secrets-of-squid-skin/">sophisticated camouflage</a> through chromatophores - pigment-filled cells controlled by the nervous system - that allow them to change color almost instantly. Some species also display bioluminescence via symbiotic bacteria or light-producing organs.



<h2 class="wp-block-heading" id="h-studying-squids-with-fossil-rocks">Studying squids with fossil rocks</h2>



The research shows that squids were already dominant ocean predators 100 million years ago. This changes what scientists believed about life in ancient seas.



The team used a new technique to scan <a href="https://www.earth.com/news/living-baby-colossal-squid-captured-on-video-for-the-first-time-ever/">fossil</a> rocks. They fully digitized the rocks in 3D without breaking them open. This helped them find over 1,000 fossilized beaks of ancient cephalopods. 



Out of these, 263 were from squids. About 40 of those belonged to species that scientists had never seen before.



<h2 class="wp-block-heading" id="h-squids-rarely-leave-fossils">Squids rarely leave fossils</h2>



Squids have soft bodies that decay quickly after death. Unlike animals with bones or shells, they leave behind very little for scientists to find. 



This makes it hard to trace their history through fossils. However, squids have tough beaks, which they use like jaws to catch and eat prey. These beaks are strong enough to survive over millions of years in rock.



Cephalopods, the group that includes squids, <a href="https://www.earth.com/news/octopuses-could-dominate-earth-if-humans-vanish/">octopuses</a>, and <a href="https://www.earth.com/news/cuttlefish-have-passed-marshmallow-test-designed-for-kids-proving-cephalopods-intelligence/">cuttlefish</a>, have existed for about 500 million years. But it’s been difficult for scientists to figure out exactly when squids first appeared and how they changed over time.



Because full squid <a href="https://www.earth.com/news/new-species-of-deep-sea-squid-discovered-that-broods-giant-eggs/">fossils</a> are rare, researchers have had limited evidence to work with. This study changes that. 



By finding hundreds of ancient squid beaks in 100-million-year-old rocks, scientists now have solid proof that squids were already present and had formed many different species. It fills in a major gap in our understanding of their ancient history.



<h2 class="wp-block-heading" id="h-ancient-squids-dominated-the-ocean">Ancient squids dominated the ocean</h2>



The researchers found more squid fossils than those of ammonites and bony fish. That came as a surprise. Ammonites had shells and were thought to be the most successful swimmers of the Mesozoic era.



“In both number and size, these <a href="https://www.earth.com/news/squid-mating-tactics-are-determined-by-birth-date/">ancient</a> squids clearly prevailed the seas,” said Dr. Shin Ikegami of the Department of Earth and Planetary Sciences at Hokkaido University, the study’s first author. 



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/06/squids_dominated-oceans_100-million-years-ago_grinding-tomography_Ikegami_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/06/squids_dominated-oceans_100-million-years-ago_grinding-tomography_Ikegami_1s.webp" alt="The digital fossil-mining method utilizes grinding tomography to create digitized rocks and reveal hidden fossils within them. Credit: Ikegami et al., Science" class="wp-image-1975747"/></a><figcaption class="wp-element-caption">The digital fossil-mining method utilizes grinding tomography to create digitized rocks and reveal hidden fossils within them. Click image to enlarge. Credit: Ikegami et al., Science</figcaption></figure>



“Their body sizes were as large as fish and even bigger than the ammonites we found alongside them. This shows us that squids were thriving as the most abundant swimmers in the ancient ocean.”



<h2 class="wp-block-heading" id="h-modern-squids-in-ancient-oceans">Modern squids in ancient oceans</h2>



The study found that <a href="https://en.wikipedia.org/wiki/Myopsida" target="_blank" rel="noreferrer noopener">Myopsida</a> and <a href="https://en.wikipedia.org/wiki/Oegopsida" target="_blank" rel="noreferrer noopener">Oegopsida</a> squids existed 100 million years ago. These two groups are still present today. Myopsida live near the shore. Oegopsida live in the open ocean.



Earlier theories suggested ancient squids evolved rapidly after the extinction of the <a href="https://www.earth.com/news/where-did-dinosaurs-come-from-missing-fossils-hold-the-secret/">dinosaurs</a>. That extinction happened 65 million years ago. But this study shows squids had already diversified long before that event.



<h2 class="wp-block-heading" id="h-early-apex-hunters">Early apex hunters</h2>



Associate Professor Yasuhiro Iba of the Department of Earth and Planetary Sciences at <a href="https://www.global.hokudai.ac.jp" target="_blank" rel="noreferrer noopener">Hokkaido University</a> led the study.



“These findings change everything we thought we knew about marine ecosystems in the past,” said Iba. “Squids were probably the pioneers of fast and intelligent swimmers that dominate the modern ocean.”



The new fossil data shows that squids had already taken important roles in the ocean. They were not just survivors. 



They were already key predators in their ecosystems. Their numbers, size, and early diversity support that conclusion.



<h2 class="wp-block-heading" id="h-rethinking-ocean-evolution">Rethinking ocean evolution</h2>



Squids are among the most active, adaptable, and intelligent invertebrates living in today’s oceans. They use complex behaviors, advanced movement, and sharp sensory skills to survive in both coastal and deep-sea environments. 



Because of their importance in modern <a href="https://www.earth.com/news/fishing-removes-key-nutrients-from-marine-ecosystems/">marine ecosystems</a>, understanding their origins can help scientists piece together the long history of ocean life.



By studying when ancient squids first appeared and how they spread into different habitats, researchers can trace the development of major evolutionary traits. These include fast swimming, hunting techniques, and even early signs of intelligence. 



Such insights also offer a clearer picture of how ancient marine ecosystems functioned and how they changed over time.



This new study provides strong evidence that many squid species were already established and thriving 100 million years ago - long before the mass extinction that ended the age of dinosaurs. 



Their presence was not small or recent. Instead, they played a major role in shaping ocean life far earlier than we previously believed.



The study is published in the journal <a href="https://www.science.org/doi/10.1126/science.adu6248" target="_blank" rel="noreferrer noopener">Science</a>.



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Squids dominated ancient oceans 100 million years ago

When we imagine the ancient oceans, we often picture massive...

Earth’s oceans keep long, detailed logs of climate change, and some of the best pages come from fusulines - shells smaller than a grain of sand. 



A recent study shows that these tiny record‑keepers flourished when the planet cooled yet nearly vanished, twice, when volcanic heat spiked global temperatures.



The work was led by Professor Shuzhong Shen of <a href="https://www.nju.edu.cn/en/" target="_blank" rel="noreferrer noopener">Nanjing University</a>. The research team stitched together 299 rock sections and 1,391 fossil <a href="https://www.earth.com/news/scientists-finally-confirm-species-identity-of-the-dragon-man-fossil-skull-denisovan/">species</a> to build an unusually sharp picture of past marine life.



<h2 class="wp-block-heading" id="h-fusulines-recorded-carbon-changes">Fusulines recorded carbon changes</h2>



The stars of the study are <a href="https://www.bgs.ac.uk/discovering-geology/fossils-and-geological-time/foraminifera/" target="_blank" rel="noreferrer noopener">foraminifera</a>, single‑celled protists that build carbonate shells. One order, Fusulinida, blanketed the seafloor from 344 million to 252 million years ago and behaved like “carbonate rock factories,” pumping out vast reefs as they grew.



Shen’s data reveal two bursts of diversification, one during late <a href="https://www.nationalgeographic.com/science/article/carboniferous" target="_blank" rel="noreferrer noopener">Carboniferous</a> cooling and another as the <a href="https://www.britannica.com/science/Permian-Period" target="_blank" rel="noreferrer noopener">Permian</a> began. 



The first wave produced small, simple shells; the second favored larger forms with honeycomb‑like walls that likely hosted photosynthetic <a href="https://www.earth.com/news/fossil-discovery-pushes-back-reptile-evolution-by-40-million-years/">partners</a>.



<h2 class="wp-block-heading" id="h-fusulines-declined-in-warm-spikes">Fusulines declined in warm spikes</h2>



When the climate <a href="https://www.science.org/doi/10.1126/science.aba6853" target="_blank" rel="noreferrer noopener">cooled</a>, glaciers locked up water, sea levels dropped, and new shallow habitats opened. Fusuline species counts tripled during that 40‑million‑year chill, echoing a pattern seen in later planktonic cousins during the Cenozoic cooling trend.



Warm pulses told a different story. The Kasimovian warming about 304 million years ago wiped out roughly 45 percent of fusuline species in less than one million years, and the curve plunged again as temperatures climbed between 294 million and 284 million years ago.



The end‑Permian supervolcano sealed their fate. During that episode, 59.5 percent of remaining species disappeared in a window shorter than the span between human <a href="https://www.earth.com/news/what-modern-fossils-will-be-the-most-surprising-to-future-explorers/">generations</a> today.



<h2 class="wp-block-heading" id="h-carbon-from-volcanoes-drove-extinctions">Carbon from volcanoes drove extinctions</h2>



Shen’s timeline lines up each extinction spike with a pulse of basalt from giant volcanic provinces such as Emeishan and Siberia. 



Those eruptions injected <a href="https://www.nature.com/articles/ngeo3031" target="_blank" rel="noreferrer noopener">carbon dioxide</a> fast enough to heat surface oceans by 5 to 10 °F, acidify seawater, and strip it of oxygen, a triple hit <a href="https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/benthic-organisms" target="_blank" rel="noreferrer noopener">benthic organisms</a> could not dodge.



Carbon‑isotope <a href="https://www.pnas.org/content/111/9/3316" target="_blank" rel="noreferrer noopener">data</a> show the oceans turned more acidic whenever the 87Sr/86Sr ratio dipped, a fingerprint of fresh volcanic rock weathering. 



At the same time, modeled oxygen levels dropped below the threshold needed to support large seafloor life - matching modern observations where foraminiferal diversity declines sharply in low-oxygen zones



<h2 class="wp-block-heading" id="h-orbital-cycles-mattered-less">Orbital cycles mattered less</h2>



Beyond the headline crashes, Shen’s team spotted weak but persistent <a href="https://science.nasa.gov/science-research/earth-science/milankovitch-orbital-cycles-and-their-role-in-earths-climate/" target="_blank" rel="noreferrer noopener">Milankovitch cycles</a>, grand wobbles in Earth’s orbit that last around two million and one million years. 



During the minima of those cycles, gentler seasons may have favored glacier growth and nutrient runoff, nudging speciation upward.



The cycles explain no more than ten percent of the diversity curve, yet their fingerprint is clear enough to remind us that even slow orbital nudges modulate life. 



Still, the sharpest rises and falls match rapid volcanic events, confirming that climate severity, not orbital pacing, set the main tempo.



<h2 class="wp-block-heading" id="h-carbon-rise-threatens-ocean-life-again">Carbon rise threatens ocean life again</h2>



“Mitigating climate change and protecting ecosystems is an urgent task of our time,” emphasized Professor Shen. The study’s most sobering line compares rates of <a href="https://www.earth.com/news/fossil-euarthropod-youti-yuanshi-lived-520-million-years-ago-insect-evolution/">ancient</a> warming with today’s rates.&nbsp;



Current <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC12060277/" target="_blank" rel="noreferrer noopener">human‑driven warming</a> runs at least ten times faster than the pace that eliminated fusulines, and modern reef‑building calcifiers already show stress in warmer, more acidic seas. 



If past is prologue, sustained greenhouse gas emissions could push today’s carbonate shell builders, corals, coccolithophores, large benthic foraminifera, toward the same cliff.



<h2 class="wp-block-heading" id="h-carbon-linked-extinction-cycles">Carbon-linked extinction cycles</h2>



To reach sub‑45,000‑year resolution, the team fed every first‑ and last‑appearance datum into a constrained‑optimization algorithm called <a href="https://www.nhm.uio.no/english/research/resources/past/help/conop.html" target="_blank" rel="noreferrer noopener">CONOP</a>. 



Supercomputers iterated millions of possible stratigraphic orders until the tightest fit emerged, turning scattered field data into a single high‑definition timeline.



Rarefaction tests showed that sampling gaps do not skew the pattern; three different resample sizes reproduced the same peaks and troughs. 



By filtering out trends longer than ten million years, the researchers isolated the shorter cycles that hint at orbital pacing.



<h2 class="wp-block-heading" id="h-the-rise-and-fall-of-fusulines">The rise and fall of fusulines</h2>



The experts then ran multivariate regressions against seven environmental proxies, from carbon isotopes to sea‑level curves. 



The best model, which combines carbon dioxide, seawater strontium, oxygen availability, and carbon isotopes, explains 81 percent of the diversity swings, leaving little doubt that physical climate set the rules of life and death for fusulines.



Fusulines vanished, but their story still speaks. They show that rapid warming can silence even dominant, resilient lineages, and they underline how cooling phases can seed explosive innovation.



Marine ecosystems today sit at a similar junction, with greenhouse gases climbing and volcanic analogs replaced by smokestacks and exhaust pipes. 



The fossil record offers no comfort that life can adapt at the speed we are forcing, but it does offer a clear warning.



The study is published in the journal <a href="https://www.science.org/doi/10.1126/sciadv.adv2549" target="_blank" rel="noreferrer noopener">Science Advances</a>.



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Tiny ocean creatures have always gone extinct during Earth's past climate warming periods

Earth’s oceans keep long, detailed logs of climate change, and...

We know the oceans are changing. But how have they changed over the last half-billion years? Until now, we had no clear measure of how the total mass of ocean life - not just its variety - has evolved over deep time. 



In a first-of-its-kind effort, scientists from <a href="https://www.stanford.edu/">Stanford University</a> measured how the biomass of marine organisms - the actual amount of living material in the ocean - has changed over the last 540 million years.



<h2 class="wp-block-heading" id="h-long-term-changes-in-ocean-life">Long-term changes in ocean life</h2>



The study shows a long-term trend of rising <a href="https://www.earth.com/news/deforestation-causes-biomass-loss-beyond-directly-affected-areas/">biomass</a>, with noticeable crashes during major extinction events. This pattern closely tracks with known increases in marine biodiversity, suggesting a deep link between how much life the ocean holds and how varied that life is.



Study lead author Pulkit Singh is a postdoctoral scholar in Earth and Planetary Sciences in the <a href="https://sustainability.stanford.edu/">Stanford Doerr School of Sustainability</a>.



“Understanding the amount of biomass is important because it represents key traits about an ecosystem that are not captured by the number of species or even the number of niches that they fill,” said Singh.



“But as we move into the past, our measurements of biomass are very limited, so that was the big gap in biological history we wanted to fill with our study.”



<h2 class="wp-block-heading" id="h-ocean-life-changes-across-history">Ocean life changes across history</h2>



Getting to this result took years of meticulous work. Singh and his team dug into data from over 7,700 marine limestone samples spanning hundreds of millions of years. 



The samples came from more than 100 published studies and Singh’s own data collection. Each rock was cut and polished into slices thin enough for light to pass through, then examined under a microscope. 



Using a method called petrographic point-counting, the researchers calculated what percentage of each sample was made up of skeletal remains - <a href="https://www.earth.com/news/fossilized-shells-can-help-predict-the-impacts-of-climate-change/">shells</a> from animals, certain algae, and single-celled protists.



It’s not just busywork. The amount of shell material in these rocks tells scientists how much living material existed at different points in Earth’s history. 



More shells in the ocean generally mean more <a href="https://www.earth.com/news/all-living-things-emit-a-subtle-glow-that-ceases-at-death/">living things</a>. And more life usually means more energy flowing through ecosystems - a strong signal of planetary health.



<h2 class="wp-block-heading" id="h-the-challenge-of-measuring-biomass">The challenge of measuring biomass </h2>



Tracking <a href="https://www.earth.com/news/global-biodiversity-crisis-is-actually-worse-than-we-thought/">biodiversity</a> through deep time has been part of science since the 19th century. But measuring biomass - the total amount of living material - is a much rarer effort. 



Measuring biomass demands massive amounts of data and offers no guarantee of a clear pattern.



“The first quantitative effort to document and graph biodiversity across geological time was made in 1860, but until Pulkit’s paper, there’s never been a corresponding biomass-across-time paper,” noted senior study author Professor Jonathan Payne. 



“I’m impressed by his intellectual courage to go and take a chance on a project like this.”



<h2 class="wp-block-heading" id="h-biomass-over-millions-of-years">Biomass over millions of years</h2>



The earliest rocks examined, from the Cambrian period about 540 million years ago, showed low shell content - under 10 percent on average. 



By the Ordovician, starting around 485 million years ago, shell percentages rose. This increase lines up with the Cambrian Explosion, a period when life rapidly diversified.



Early on, sponges were major players. Later, they were overtaken by echinoderms (ancestors of starfish) and arthropods like trilobites. 



<h2 class="wp-block-heading" id="h-a-gradual-increase-in-biomass">A gradual increase in biomass </h2>



Over the next 230 million years, shell content stayed mostly above 20 percent, aside from big dips during <a href="https://www.earth.com/news/marine-life-became-strangely-uniform-after-earths-worst-mass-extinction/">mass extinctions</a>.



One of the sharpest declines came during the Permian-Triassic extinction about 250 million years ago - the “Great Dying.” Shell material dropped to just 3 percent. 



Life rebounded after that, although smaller setbacks followed during the end-Triassic and the well-known Cretaceous-Paleogene extinction 66 million years ago.



In our current era - the Cenozoic - shell volume climbed above 40 percent, boosted by creatures like mollusks and corals. “The overall pattern that we were able to capture is that it’s a gradual increase,” Singh said.



<h2 class="wp-block-heading" id="h-consistent-biological-patterns">Consistent biological patterns </h2>



The team knew they had to rule out alternative explanations. Maybe shell-boring predators were less common in the past. Maybe certain environments were overrepresented in the data. 



To check, the researchers sorted samples by depth, latitude, and geological setting. The trend held steady.



“The more tests we did and the more we divided our dataset, we realized that these big biological patterns we were seeing stayed over time,” Singh said.



<h2 class="wp-block-heading" id="h-why-did-ocean-life-keep-growing">Why did ocean life keep growing?</h2>



The answer may come down to diversity. As life evolved to fill more ecological roles, it got better at using available energy. Organisms became more specialized, more interconnected. 



That allowed ecosystems to recycle nutrients more efficiently - from sunlight-eating phytoplankton to decomposers returning nutrients to the cycle.



“The overall idea is that there is more food available in ecosystems and because of that, the ecosystems can support more life, there’s more energy available, and that leads to greater abundance expressed in biomass,” Singh said.



<h2 class="wp-block-heading" id="h-humans-are-rapidly-changing-ocean-life">Humans are rapidly changing ocean life</h2>



The study paints a long view of life’s upward climb, but it ends before the modern age. Today’s oceans face threats from overfishing, pollution, acidification, and climate change. 



Researchers agree - we’re already in the middle of a human-caused sixth mass extinction. And if biodiversity keeps falling, we may see long-term drops in biomass too - with effects that could last millions of years.



“From our study’s perspective, modern times are quite complicated given the extent of human activity that’s rapidly altering conditions planetwide, including in the oceans,” said Payne. 



“But our findings show that overall biomass is linked to biodiversity and that losses in biodiversity may suppress productivity for geologically meaningful intervals, adding one more argument of why conserving biodiversity is essential for the health of humans and our planet.”



The full study was published in the journal <a href="https://linkinghub.elsevier.com/retrieve/pii/S0960982225007353">Current Biology</a>.



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Fossils reveal 500 million years of changes in ocean life

We know the oceans are changing. But how have they...

For 50 years, scientists believed that fish schools saved energy by swimming in diamond formations. This view, rooted in models by Weihs and Lighthill from the 1970s, shaped decades of research and robotic design. 



However, new research from <a href="https://www.princeton.edu" target="_blank" rel="noreferrer noopener">Princeton</a> and <a href="https://www.harvard.edu" target="_blank" rel="noreferrer noopener">Harvard</a> scientists turns that theory on its head. <a href="https://www.earth.com/news/small-fish-species-are-the-big-catch-of-the-future/">Fish</a> don't move in neat, flat diamonds. Instead, they prefer dynamic, three-dimensional ladders.



<h2 class="wp-block-heading" id="h-a-new-look-at-fish-schooling-patterns">A new look at fish schooling patterns</h2>



The researchers tracked six giant danios swimming continuously for ten hours in a recirculating flow tank. They used synchronized side and bottom cameras, along with deep learning software, to collect detailed 3D data on fish positions. 



This advanced setup allowed the team to record over 260,000 frames where at least four fish were clearly visible and trackable from both views.



The findings challenged long-held assumptions about fish schooling patterns. Only 0.1% of the frames showed fish in the classical diamond formation, long thought to be the most energy efficient. 



<h2 class="wp-block-heading" id="h-fish-mostly-swim-in-ladders">Fish mostly swim in ladders</h2>



Instead, the fish predominantly adopted a new three-dimensional arrangement termed the ladder formation. In this pattern, <a href="https://www.earth.com/news/small-fish-provide-climate-resilient-nutrition-for-a-warming-world/">fish</a> were staggered vertically, with some swimming slightly above or below others, rather than maintaining a flat side-by-side structure.



The ladder pattern appeared in 79% of fish pairings, making it by far the most common. Additionally, only 25.2% of all fish pairs swam in the same horizontal plane. This indicates that vertical positioning is a key feature of natural fish school behavior, something that earlier two-dimensional studies overlooked. 



The study reveals that fish prefer dynamic 3D arrangements that likely reduce drag without requiring precise alignment.



<h2 class="wp-block-heading" id="h-why-the-fish-ladder-works">Why the fish ladder works</h2>



“When swimming, <a href="https://www.earth.com/news/how-alternative-seafood-can-help-save-our-oceans/">fish</a> on average generate a jet going backward, like the jet engine of a plane,” said Hungtang Ko, lead author of the study. Staying out of that jet reduces drag.



The ladder formation allows this. A fish swims slightly above or below the one in front, avoiding the jet while still staying close. This creates energy savings similar to the diamond model but with less need for perfect timing or alignment.



The diamond model assumes fish must synchronize tail beats and stay level. But in real schools, coordination varies. Fish rarely beat tails in exact anti-phase, a condition the diamond pattern needs to be effective.



Even in controlled experiments, <a href="https://www.earth.com/news/fish-are-quietly-battling-climate-change-on-the-seabed/">fish</a> constantly rearranged positions. The average pattern changed every 48 seconds for individuals and 32 seconds for the whole school.



Ko’s team observed that fish ladder formations shift based on flow rate. As speed increased from 1.6 to 5.6 body-lengths per second, the fish ladder stretched longer. This adaptation resembled behavior in other biological collectives, like fire ant rafts.



<h2 class="wp-block-heading" id="h-tracking-fish-in-three-dimensions">Tracking fish in three dimensions</h2>



Older studies limited fish to shallow tanks or still water, forcing unnatural formations. This experiment used deeper tanks and steady flow, removing boundary effects. 



The researchers trained AI to detect nose and tail positions in 3D space using SLEAP.ai and a custom MATLAB pipeline.



According to the heatmaps, fish were most likely to swim either above and behind, or below and ahead, of a partner - never directly inline.



This ladder structure formed naturally, not by training or conditioning. It shows how real-world conditions reshape what we think of as “efficient.”



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



The Nagpal lab is designing robot fish swarms inspired by these new insights. By mimicking ladder formations, underwater robots might conserve energy, move more smoothly, and navigate better in tasks like reef monitoring.



“The collaboration is a two-way street,” said Ko. “We can use computer vision to discover how and why animal groups do things together. And then we can ask, what kind of real-world robotic system could this biological insight be applied to?”



<h2 class="wp-block-heading" id="h-fish-schools-conserve-energy">Fish schools conserve energy </h2>



This study shows that energy savings don’t come from holding a perfect formation. Instead, savings come from many temporary, varied arrangements. 



Even fish that constantly shift positions still gain benefits by staying out of each other's wake.



The study also raises new questions. Can robot fish switch positions while still conserving energy? Do vertical ladders work better in turbulent water? Future experiments, especially using robotic models, may find answers.



For now, one thing is certain. Nature prefers complexity over perfection. Fish don't swim in flat diamonds. They climb invisible ladders, one body length at a time.



The study is published in the journal <a href="https://www.nature.com/articles/s41598-025-06150-2" target="_blank" rel="noreferrer noopener">Scientific Reports</a>.



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Fish swim in schools by stacking like ladder rungs

For 50 years, scientists believed that fish schools saved energy...

Climate, geology, and biology together gave rise to one of Earth’s most dramatic turning points: the Cambrian explosion. About 530 million years ago, most of the basic body plans of organisms that have survived until now emerged.



Yet a new study argues that key elements of this revolutionary event actually took shape earlier - perhaps ten-plus million years before the formal start of the Cambrian Period.



The research relies not on bones or shells, but on trace fossils - the tracks, burrows, and other imprints left by organisms as they crawled through ancient sediments.



Co-authors Olmo Miguez Salas of the <a href="https://web.ub.edu/web/ub/">University of Barcelona</a> and Zekun Wang of London’s <a href="https://www.nhm.ac.uk/">Natural History Museum</a> analyzed these subtle signatures. 



The goal was to reconstruct early animal anatomy and behavior during the Ediacaran-Cambrian transition, roughly 545 million years ago.



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



Traditional fossil studies skew toward creatures with hard parts, because bones and shells preserve most readily in rock. Trace fossils capture a different story: the activities of <a href="https://www.earth.com/news/earths-first-animals-were-very-picky-about-where-they-lived/">soft-bodied animals</a> that rarely leave skeletal remains.



“The trace fossil record provides valuable information about evolutionary periods when soft-bodied fauna were dominant,” Miguez Salas said.



“Fossil traces reflect the behavior of the organism that generates them, which is determined by habitat and responses to environmental stimuli. Therefore, they are an indicator of the palaeoecological conditions in which the organisms that generated them lived.”



That focus is especially useful for the Ediacaran-Cambrian boundary, a time when soft-bodied organisms still outnumbered shelly ones and ecological dynamics were in rapid flux.



Early burrowers and crawlers disturbed microbial mats on the seafloor. This paved the way for new feeding strategies, novel body plans, and ultimately the hard-part explosion more familiar to paleontologists.



<h2 class="wp-block-heading" id="h-fossils-show-how-life-moved">Fossils show how life moved</h2>



By quantifying the widths, lengths, and winding patterns of fossil trackways such as Archaeonassa, Gordia, Helminthopsis, and Parapsammichnites, the team derived scaling laws that link track size to the animals’ own proportions. 



The results show that organisms with streamlined, elongated profiles were already active 545 million years ago.



“These organisms probably possessed coelomic hydrostatic bodies, with an anteroposterior axis, muscles, and possibly segmentation,” Miguez Salas said.



“Furthermore, these organisms could move in a specific direction (directional <a href="https://www.earth.com/news/not-all-kangaroo-ancestors-hopped-as-a-means-of-locomotion/">locomotion</a>) and probably possessed sensory capabilities to move and feed on heterogeneous substrates in a habitat dominated by microbial mats.”



<h2 class="wp-block-heading" id="h-traits-predate-cambrian-explosion">Traits predate Cambrian explosion</h2>



Such abilities - directional crawling, muscular movement, possible segmentation - echo the hallmarks of bilaterian animals that dominate the modern biosphere. 



If those traits existed well before 530 million years ago, then the lineage-splitting events that scientists historically assign to the Cambrian must have roots in the late <a href="https://www.earth.com/news/591-million-years-ago-complex-life-emerged-on-earth-magnetic-field-ediacaran-period/">Ediacaran</a>.



“Therefore, the so-called Cambrian explosion and its evolutionary implications may have occurred much earlier than estimated,” Miguez Salas added.



Instead of a sudden burst, the data point toward a protracted interval of experimentation. Ecological engineering by active burrowers created niches that later organisms exploited.



<h2 class="wp-block-heading" id="h-math-reveals-ancient-mobility">Math reveals ancient mobility</h2>



Until now, suggestions of pre-Cambrian complexity leaned heavily on qualitative observations - isolated sites showing possible bilateral tracks or ambiguous body impressions. What sets the new paper apart is its mathematical approach.



The authors modeled modern track size to body length, then applied that scaling framework to ancient trace fossils. The outcome is a statistically grounded estimate of early animal width, length, and locomotion speed.



“This new discovery opens the door to quantitatively study future Ediacara trace fossils and to corroborate that the explosion did not happen in the Cambrian, but many millions of years earlier,” Miguez Salas said.



The same scaling rules could probe other critical transitions, such as the <a href="https://www.earth.com/news/tiny-worms-sparked-explosive-evolutionary-period-of-life-on-earth/">Great Ordovician Biodiversification Event</a>, offering a consistent yardstick for comparing evolutionary shifts across geologic time.



<h2 class="wp-block-heading" id="h-fossils-shift-life-s-timeline">Fossils shift life’s timeline</h2>



If complex bilaterians were shaping seafloor habitats 545 million years ago, paleontologists must rethink long-held assumptions. Environmental and genetic triggers like <a href="https://www.earth.com/news/rewrite-the-textbooks-life-on-earth-did-not-arise-due-to-increased-oxygen-levels/">oxygen</a> rise, ocean shifts, or gene changes may need rethinking for the Cambrian proper. 



Those factors may have been in motion earlier, with the visible “explosion” marking only the point when hard parts made diversity easier to preserve.



The study also underscores how behaviors - burrowing, mat-grazing, sediment mixing - can serve as evolutionary catalysts. Mobile animals turning over sediment could have unleashed nutrients, altered <a href="https://www.earth.com/news/microbes-laid-the-foundation-for-early-life-on-earth/">microbial communities</a>, and spurred arms races that drove further innovation.



<h2 class="wp-block-heading" id="h-what-fossils-may-still-reveal">What fossils may still reveal</h2>



Future expeditions into late Ediacaran strata may uncover additional trace fossil assemblages to test the new timeline. 



High-resolution 3D scans, geochemical proxies, and refined radiometric dating can link track-making horizons to precise ages and environmental conditions.



Meanwhile, the mathematical framework introduced by Miguez Salas and Wang equips researchers worldwide to translate faint surface scribbles into vivid portraits of Earth’s earliest movers and shakers.



In shifting the Cambrian explosion’s fuse back several million years, the fossil record reminds us that life’s history often blurs textbook boundaries. Evolution, like geology itself, tends to roll out gradually - until we gather the evidence to see its subtler steps.



The study is published in the journal <a href="https://pubs.geoscienceworld.org/gsa/geology/article/doi/10.1130/G53332.1/655874/Quantitative-decoding-of-Ediacaran-locomotory">Geology</a>.



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Cambrian explosion: Fossils push back the rise of complex life

Climate, geology, and biology together gave rise to one of...

We used to think leopard seals had broad diets, but new research suggests that many individuals are picky eaters - with big consequences.



While the species as a whole eats many prey types, <a href="https://www.earth.com/news/harbor-seals-rely-on-visual-cues-to-navigate-cloudy-waters/">individual</a> seals often specialize. This pattern has ecosystem-wide effects, especially in the predator-rich waters off Cape Shirreff.



<h2 class="wp-block-heading" id="h-leopard-seals-prefer-specific-diets">Leopard seals prefer specific diets</h2>



The research team analyzed stable isotope values (δ15N and δ13C) from 46 whiskers of 34 seals. This long-term data covered a decade. 



The results showed that 59% of the seals were dietary specialists, 28% were intermediates, and only 13% were true generalists.



Specialists fall into two categories. High trophic level specialists likely hunt fur <a href="https://www.earth.com/news/seal-pregnancies-reveal-clues-for-treating-birth-complications/">seal</a> pups and large fish. Medium to low trophic level specialists target krill, penguins, and cephalopods. 



The research suggests that individual differences in diet shape local food webs more than previously assumed.



“Even though leopard seals as a species eat a wide variety of prey, most individuals actually focus on just a few types of food,” said study co-author Dr. Emily Sperou from <a href="https://www.baylor.edu" target="_blank" rel="noreferrer noopener">Baylor University</a>. 



“This means that a few highly specialized seals can have a much bigger effect on certain prey populations than we previously thought.”



<h2 class="wp-block-heading" id="h-some-seal-diets-don-t-change">Some seal diets don’t change</h2>



The study revealed two long-term foraging styles. Some individuals, like seal 397, maintained high trophic level specialization for up to ten years. 



Others, like seal 12, changed diets significantly across five years, from specialist to generalist.



This variability suggests behavioral flexibility. <a href="https://www.earth.com/news/elephant-seals-provide-a-window-into-the-oceans-twilight-zone/">Seals</a> might shift strategies depending on prey availability or competition. Such changes could buffer the species against ecosystem shifts.



“A few specialists can help shape entire ecosystems,” said study co-author Dr. Patrick Charapata. 



“Understanding these patterns in leopard seals and other top predators can help us better predict and manage changes to prey populations and the greater ecosystem these species live in.”



<h2 class="wp-block-heading" id="h-leopard-seal-diets-and-prey-populations">Leopard seal diets and prey populations </h2>



Larger female leopard seals were found to consistently feed at higher trophic levels compared to males. This means they targeted prey that are themselves predators or occupy higher positions in the food web. 



Interestingly, all the individuals identified as high-level dietary specialists in the study were female. Their greater body size likely plays a key role in this pattern. 



Bigger <a href="https://www.earth.com/news/weddell-seals-have-a-surprising-survival-strategy/">seals</a> are physically capable of capturing and consuming larger, more energy-dense prey, such as Antarctic fur seal pups. This access to richer food sources gives them an energetic advantage and increases their impact on prey populations.



<h2 class="wp-block-heading" id="h-individuals-with-a-large-impact">Individuals with a large impact</h2>



The data also showed that females had broader isotopic ranges in their whisker samples. This suggests they influence a wider range of the ecosystem through their feeding habits. They do not just eat more; they affect more parts of the food web.



A few large females were found to be responsible for most of the observed predation on fur seal pups. One individual, identified as seal 397, stood out in particular. She had the highest number of recorded pup captures in the study. 



Her method involved ambush style attacks, showing strategic hunting behavior that likely made her even more effective. This highlights how a small number of powerful individuals can have an outsized effect on an ecosystem.



<h2 class="wp-block-heading" id="h-diets-change-with-prey-numbers">Diets change with prey numbers</h2>



The data revealed a sharp drop in δ15N values between 2015 and 2017. This trend aligns with a known decline in Antarctic fur seals and some penguin species. Researchers believe the drop reflects a reduction in nitrogen-rich prey.



From 2017 to 2023, the number of leopard seals at Cape Shirreff fell by 76 percent. The few that remained, like seal 397, regained access to higher trophic prey. As competition dropped, δ15N values began rising again.



The study reshapes how we think about predator roles. Individual specialization can reshape ecosystems. Just a few high-impact predators may shift prey dynamics dramatically.



For instance, a pod of five orcas once consumed 8,500 sea otters annually. Leopard seals may be exerting similar pressure on fur seal colonies.



Current conservation strategies often assume that all individuals in a species behave alike. But this study warns against such assumptions. Ignoring individual-level behavior might cause poor management decisions, especially under climate stress.



<h2 class="wp-block-heading" id="h-leopard-seals-and-prey-dynamics">Leopard seals and prey dynamics</h2>



The study relied on stable isotope data but did not include direct prey identification. Future research could pair isotopic signatures with tracking and observational data.



While this study was focused on Cape Shirreff, genetic data indicate that these findings may apply to leopard seals across the Southern Ocean.



The research shows how a few individual predators can shape the fates of entire species. Leopard seals remind us that even in the coldest oceans, personal dietary choices matter.



The study is published in the journal <a href="https://onlinelibrary.wiley.com/doi/10.1002/ece3.71593" target="_blank" rel="noreferrer noopener">Ecology and Evolution</a>.



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Leopard seal diets are reshaping Antarctic ecosystems

We used to think leopard seals had broad diets, but...

Once thought unique to humans, grief may exist in other species too. New research from Osaka University shows that Japanese macaques react to dying and dead group members with surprising emotion.



Published in the journal Primates, the study reveals responses beyond mothers mourning infants. It focuses instead on how macaques behave around dying or deceased adult <a href="https://www.earth.com/news/assamese-macaques-show-how-aging-affects-our-social-networks/">companions</a>.



<h2 class="wp-block-heading" id="h-macaques-stay-near-dying-friends-nbsp">Macaques stay near dying friends&nbsp;</h2>



Japanese macaques live in complex societies and form long-term grooming partnerships. Researchers tracked grooming and proximity over several years to explore whether social <a href="https://www.earth.com/news/social-tolerance-helps-monkeys-pass-along-new-skills/">closeness</a> influenced their behavior during death-related events.



“It’s incredibly rare to document these kinds of behaviors in wild animals,” said lead author Masayuki Nakamichi from <a href="https://www.osaka-u.ac.jp/en" target="_blank" rel="noreferrer noopener">Osaka University</a>. 



Macaques with strong grooming histories often stayed close to the deceased. Others kept their distance, especially when they had no prior bond.



<h2 class="wp-block-heading" id="h-visible-decay-alters-behavior">Visible decay alters behavior</h2>



Maggots played a central role in group reactions. In three of the four documented deaths, the bodies showed infestation. This strongly affected how others responded.



Monkeys typically avoided touching or approaching maggot-covered individuals. Some jumped away after sniffing the wound. Others looked and then left quickly.



Yet in one exceptional case, the group’s alpha female, Pet, groomed a dying male named Rikinio even as flies swarmed around him. She picked maggots from his back and ate them.



“The fact that some individuals remained near deceased <a href="https://www.earth.com/news/sulawesi-macaques-face-unknown-threats-from-plastic-waste/">companions</a> they had close relationships with suggests that these macaques have emotional capacities that resemble human compassion,” said study co-author Kazunori Yamada.



This behavior suggests macaques can form deep attachments and remain emotionally affected by death.



<h2 class="wp-block-heading" id="h-macaques-react-to-different-deaths">Macaques react to different deaths</h2>



Case 1 featured Rikinio, a high-ranking male wounded by a rival. Most macaques avoided him once his wound became infested. Pet alone groomed him and consumed maggots during the process.



Case 2 followed another male, K75, who declined from old age. Though his body showed no visible wounds, flies and rain had changed his appearance. Familiar group members hesitated to come near, possibly recalling his earlier condition.



Case 3 involved Pet79, a female from the dominant kin group. After returning from a long absence, she was groomed by her daughters. A month later, with maggots visible in her wounds, even close family avoided her.



Case 4 described Pet87, who died in winter. His body had no maggots. Group members remained close. A juvenile female groomed his corpse. Her mother had groomed Pet87 regularly when he was alive.



<h2 class="wp-block-heading" id="h-disease-avoidance-may-play-a-role">Disease avoidance may play a role</h2>



Macaques appear to avoid corpses showing signs of infestation. This may be a survival behavior. Avoiding flies and maggots likely reduces the risk of disease.



Many reacted by sniffing their fingers after contact or rubbing them on the ground. These actions suggest discomfort triggered by smell or touch.



When the corpse showed no damage or signs of infestation, macaques behaved calmly and remained nearby. This pattern supports the idea that visible decay, more than death itself, shapes avoidance.



<h2 class="wp-block-heading" id="h-death-awareness-in-macaques">Death awareness in macaques</h2>



Some behaviors hint at cognitive recognition of death. One low-ranking male, who avoided a higher-ranking male while alive, stayed near his corpse. Possibly, he understood the male no longer posed a threat.



Other group members hesitated to enter areas where a corpse lay still. This unusual caution may reflect recognition that something was not normal.



These findings suggest that macaques feel <a href="https://www.earth.com/news/hurricane-on-monkey-island-made-macaques-more-socially-tolerant/">emotions</a> like grief and compassion, at least in simple forms. The depth of their understanding remains unclear, but their actions show social bonds do not always end with death.



“More observations of death-related events in more species will be needed to fully understand the emotional responses of non-human primates to the dead,” said Nakamichi.



<h2 class="wp-block-heading" id="h-path-forward-in-primate-thanatology">Path forward in primate thanatology</h2>



To learn more, the researchers want to combine behavioral studies with physiological data. Measuring hormone levels, tracking stress responses, and observing reactions to smell may offer deeper insights.



Chimpanzees, for example, show aversion to the scent of putrescine, a chemical linked to decay. Similar tests in macaques may reveal if scent triggers their aversion or if vision plays a bigger role.



This study challenges long-held beliefs about grief. Japanese macaques show emotion toward the dying and dead, guided by bonds and sensory cues.



They remind us that even in the forest, empathy may bloom. Loss does not go unnoticed.



The study is published in the journal <a href="https://link.springer.com/article/10.1007/s10329-025-01196-2" target="_blank" rel="noreferrer noopener">Primates</a>.



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Japanese macaques have social bonds that persist beyond death

Once thought unique to humans, grief may exist in other...

Squid are famous for flashing from glass-clear to kaleidoscopic in the blink of an eye, but biologists have long puzzled over the physical trick behind the act.



A research team led by the <a href="https://www.uci.edu/">University of California, Irvine</a>, joined by cephalopod experts at the <a href="https://www.mbl.edu/">Marine Biological Laboratory</a> in Woods Hole, took that mystery head-on.



By peering into squid skin in three dimensions, they uncovered a hidden forest of nano-columns built from an uncommon protein called reflectin.



<h2 class="wp-block-heading" id="h-how-squid-skin-bends-light">How squid skin bends light</h2>



These columns act much like tiny mirrors, bouncing or passing light depending on how close together they sit.



Alon Gorodetsky, an expert in chemical and biomolecular engineering at UC Irvine, is the senior author of the research.



“In nature, many animals use Bragg reflectors [which selectively transmit and reflect light at specific wavelengths] for structural coloration,” he said. “A squid’s ability to rapidly and reversibly transition from transparent to colored is remarkable."



"We found that cells containing specialized subcellular columnar structures with sinusoidal refractive index distributions enable the squid to achieve such feats.”



<h2 class="wp-block-heading" id="h-studying-the-master-shapeshifter">Studying the master shapeshifter</h2>



The animals under study were longfin inshore squid, Doryteuthis pealeii. “These are longfin inshore squids – Doryteuthis pealeii – that are native to the Atlantic Ocean,” Gorodetsky said.



“Marine Biological Laboratory has been famous for studying this squid and other cephalopods for more than a century. We were fortunate to be able to leverage their world-class expertise with properly collecting, handling, and studying these biological specimens.”



Inside the squid mantle, shimmering cells known as iridophores - or iridocytes - hold the secret. 



To visualize them without disturbing their delicate innards, the team used holotomography, a form of quantitative phase microscopy that maps how <a href="https://www.earth.com/news/physicists-succeed-in-converting-light-into-a-supersolid-that-flows-like-a-liquid/">light</a> bends through a sample.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/06/squid-skin_color-change_montage_credit-UCIrvine_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/06/squid-skin_color-change_montage_credit-UCIrvine_1s.webp" alt="Digital camera images of the entire body (top left) and dorsal mantle (top right) of a squid show the splotches' blue, green, yellow, orange and red iridescent (angle-dependent) colors. An individual splotch (bottom, from left) transitions from transparent to red to orange to green at 0, 60, 90 and 120 seconds, respectively, when subjected to chemical and neurophysiological stimuli. Credit: Alon Gorodetsky Lab, UC Irvine" class="wp-image-1975656"/></a><figcaption class="wp-element-caption">Digital camera images of the entire body (top left) and dorsal mantle (top right) of a squid show the splotches' blue, green, yellow, orange and red iridescent (angle-dependent) colors. An individual splotch (bottom, from left) transitions from transparent to red to orange to green at 0, 60, 90 and 120 seconds, respectively, when subjected to chemical and neurophysiological stimuli. Click image to enlarge. Credit: Alon Gorodetsky Lab, UC Irvine</figcaption></figure>



Georgii Bogdanov, a postdoctoral researcher in chemical and biomolecular engineering at UC Irvine, is another lead author of the study.



“Holotomography used the high refractive index of reflectin proteins to reveal the presence of sinusoidal refractive index distributions within squid iridophore cells,” he said.



Reflectin platelets form spiral columns inside iridophores, enabling cephalopods to control how their skin transmits and reflects light.



<h2 class="wp-block-heading" id="h-borrowing-nature-s-blueprint"><a></a>Borrowing nature’s blueprint</h2>



Once the researchers understood the architecture - the stacked, spiraling Bragg reflectors - they wondered whether they could engineer something similar.



Studying squid color change inspired flexible materials that shift appearance using tiny, wavy Bragg reflector columns. They added nanostructured metal films, enabling the materials to also shift appearance in the infrared spectrum.



Using a mixture of polymer chemistry, nanofabrication, and metal coatings, the group built thin films that shift color when stretched, pressed, or heated. 



They went a step further by tailoring the same films to tune their <a href="https://www.earth.com/news/mosquitoes-use-thermal-infrared-vision-to-track-and-bite-humans/">infrared</a> emission. This allows the material to hide or reveal heat signatures as well as visible hues.



“These bioinspired materials go beyond simple static color control, as they can dynamically adjust both their appearances in the visible and infrared wavelengths in response to stimuli,” said co-author Aleksandra Strzelecka, a PhD student at UC Irvine.



“Part of what makes this technology truly exciting is its inherent scalability," she said. "We have demonstrated large-area and arrayed composites that mimic and even go beyond the squid’s natural optical capabilities."



This opens the door to many applications ranging from adaptive <a href="https://www.earth.com/news/how-squid-power-their-amazing-camouflage-abilities/">camouflage</a> to responsive fabrics to multispectral displays to advanced sensors.



<h2 class="wp-block-heading" id="h-future-optics-from-squid-skin">Future optics from squid skin</h2>



The implications stretch far beyond a novelty coating. The same Bragg-style stacks could sharpen laser output, filter signals in fiber-optic lines, and boost solar-cell efficiency. They could also enable real-time structural health monitoring in bridges and aircraft.



“This study is an exciting demonstration of the power of coupling basic and applied research,” Gorodetsky said. “We have likely just started to scratch the surface of what is possible for cephalopod-inspired tunable optical materials in our laboratory.”



Every advance stemmed from squid skin cells with tiny winding columns just hundreds of nanometers wide. Despite their size, these structures could orchestrate a light show visible from meters away.



The team’s work shows how decoding those natural nanostructures can lead to devices that humans manufacture by the meter rather than by the molecule.



<h2 class="wp-block-heading" id="h-squid-inspired-tech-evolves">Squid-inspired tech evolves</h2>



Researchers aim to speed up film response and develop biodegradable versions for sensors and medical patches.



Meanwhile, the discovery reaffirms why <a href="https://www.earth.com/news/octopus-and-squid-senses-linked-to-human-brain-evolution/">cephalopods</a> remain a favorite subject for materials scientists: they are masters of manipulating light without a single pigment or battery.



In the lab, that mastery is starting to take shape as fabrics that cool soldiers in the desert by day, buildings that shimmer to reduce air-conditioning loads, and flexible screens that display both artwork and thermal data.



The next chapter, as Gorodetsky’s group sees it, will be written where biology and engineering merge. 



The squid’s split-second shape-shifting trick has journeyed from the Atlantic deep to a microscope slide and into a polymer film. 



Soon, it may appear on your jacket sleeve or smartphone case, blending vivid color with invisible infrared control just like in cephalopods.



The study is published in the journal <a href="https://www.science.org/doi/10.1126/science.adn1570" target="_blank" rel="noreferrer noopener">Science</a>.



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Scientists unlock the light-bending secrets of squid skin

Squid are famous for flashing from glass-clear to kaleidoscopic in...

Anyone who has ever tossed and turned at night knows how much sleep matters. Stress, social distractions, and even the weather can disrupt our rest. And it turns out we’re not the only ones.



Orangutans - some of our closest living relatives - face similar challenges, and they’ve figured out a relatable solution: they nap.



<h2 class="wp-block-heading" id="h-tired-minds-and-busy-days">Tired minds and busy days</h2>



Life in the rainforest is no easy task for <a href="https://www.earth.com/news/orangutans-use-complex-vocal-patterns-found-in-human-language/">orangutans</a>. Every day involves travel, food gathering, social puzzles, and constant movement - mental and physical strain is inevitable.



“Moving through the canopy, finding food, solving problems, navigating social relationships; these are all tiring and cognitively demanding tasks,” said&nbsp;Alison Ashbury, the study’s first author. 



“When an orangutan doesn’t get enough sleep, it does what any sleep-deprived human might do: it climbs into bed, lies down, and takes a nap.”



Scientists from the <a href="https://www.ab.mpg.de/">Max Planck Institute of Animal Behavior</a> (MPI-AB) and the University of Konstanz in Germany, together with collaborators at the Universitas Nasional in Indonesia, studied wild orangutans in the rainforests of Sumatra. 



The goal was to understand how these great apes manage their sleep in the wild and what that can teach us about the evolution of rest in <a href="https://www.earth.com/news/bonobos-group-cohesion-common-enemy-effect-do-not-kill-inside-their-species/">primates</a>.



<h2 class="wp-block-heading" id="h-monitoring-orangutan-bedtimes">Monitoring orangutan bedtimes</h2>



For over 14 years, the team collected behavioral data on 53 adult orangutans at the Suaq Balimbing Monitoring Station. They followed the animals through 455 days and nights, closely watching how and where they slept.



Each evening, adult orangutans build a sleeping “nest” high in the treetops. This nest acts as a bed, with branches woven together to form a secure platform. 



The orangutans even add leaves for a mattress and pillow. Mothers share nests with their nursing babies, but otherwise, adults sleep solo. At dawn, they leave the nest and begin the day.



“From our point of view on the ground, we usually can’t see orangutans at all in their night nests, but we can hear them rustling around, getting comfortable,” said Caroline Schuppli, the study’s senior author and a group leader at MPI-AB. “Eventually, everything goes quiet and still. And the reverse happens in the morning.”



The researchers measured the period of nighttime silence as a proxy for sleep. Although they couldn’t directly monitor brain activity, the length of this quiet period closely matched patterns of actual sleep observed in captive orangutans and wild <a href="https://www.earth.com/news/baboons-walk-in-lines-just-to-stay-near-their-friends/">baboons</a>. On average, orangutans slept for nearly 13 hours each night.



<h2 class="wp-block-heading" id="h-what-interrupts-orangutan-sleep">What interrupts orangutan sleep?</h2>



Several factors disrupted sleep. Orangutans had shorter sleep periods when they built their nests close to others and when nights were colder. Sleep was also reduced on days when they had traveled farther.



“We thought it was really interesting that just being near other orangutans when building a night nest was linked to shorter sleep periods,” said Ashbury. “Imagine you stay up late hanging out with your friends, or your roommate is snoring so loudly in the morning that you get up early. I think it’s a bit like that."



"They’re prioritizing being social over sleeping, or their sleep is being disrupted by others nearby, or even both.”



<h2 class="wp-block-heading" id="h-naps-after-sleepless-nights">Naps after sleepless nights</h2>



The team also explored how orangutans compensate for lost sleep. They found a consistent pattern: when orangutans had shorter nighttime sleep, they napped more during the day. In fact, for every hour less sleep the night before, they added 5 to 10 extra minutes of nap time the next day.



“For people, even a short nap can have significant restorative effects,” noted the researchers. “It’s possible that these naps are helping orangutans reset physiologically and cognitively after a poor night’s sleep, just like they do in humans.”



The orangutans used simple, quickly built day nests for these <a href="https://www.earth.com/news/how-do-afternoon-naps-impact-our-health/">naps</a>. These nests took less than two minutes to construct, lacked many of the comfort features of night nests, and were used solely for short rest periods.



“Day nests are less sophisticated, have fewer comfort elements, and are made quicker than night nests,” said Schuppli. “But even so, when we’re able to see an orangutan resting in a day nest, we see that their bodies are relaxed and their eyes are closed. They really do appear to be sleeping.”



<h2 class="wp-block-heading" id="h-naps-and-brain-power">Naps and brain power</h2>



Scientists have long recognized the Suaq orangutans for their exceptional mental abilities. Their frequent napping habits may play a role in supporting this cognitive edge.



“Among all studied orangutan populations, the Suaq orangutans arguably exhibit the widest range of cognitively demanding behaviors,” said Schuppli, who also directs research at the site. 



“This may be linked to their relatively high propensity for daytime nest use. Either they need these high-quality naps to meet their cognitive demands, or their cognitive abilities can come about because they take high-quality naps in day nests so often.”



Another possible factor is their semi-solitary lifestyle. Orangutans don’t live in tight social groups, so they’re free to nap when they feel the need. 



The data showed that orangutans took at least one nap on 41% of observed days, and those naps averaged 76 minutes.



<h2 class="wp-block-heading" id="h-lessons-from-wild-sleep">Lessons from wild sleep</h2>



“Studying sleep in the wild, in the natural social and ecological conditions under which it evolved, is important to broadening our understanding of the evolutionary origins and the ultimate functions of sleep,” said Meg Crofoot, director at MPI-AB and a professor at the University of Konstanz. 



“Why did animals, from humans to primates to spiders to jellyfish, evolve to spend such large portions of their lives in this vulnerable unconscious state? If we’re going to answer this question, we need to bring sleep research out of the lab and into the field. Studies such as this one contribute to that effort.”



Orangutans napping in leafy nests may seem like a simple sight. But their resting habits may hold deeper clues about sleep’s role in intelligence, social life, and <a href="https://www.earth.com/news/survival-of-the-fittest-study-suggests-its-more-a-game-of-chance/">survival</a> - for them and for us.



The full study was published in the journal <a href="https://linkinghub.elsevier.com/retrieve/pii/S0960982225006694">Current Biology</a>.



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Orangutans manage sleep much like humans do

Anyone who has ever tossed and turned at night knows...

Cod once ruled the Baltic Sea - massive, plentiful, and essential to the region’s fishing economy. They often stretched over a meter long and weighed up to 40 kilograms. 



Along with herring, cod once sustained industries, communities, and families. Now, they have vanished - at least in their original form. 



Catching an impressive-sized cod is a rare sight - and is no longer permitted. A ban on targeted cod fishing has been in effect since 2019, following a population collapse.



It’s not just the numbers that plummeted. Cod shrank, and the changes didn't stop at the surface level. 



<h2 class="wp-block-heading" id="h-fishing-pressure-rewired-a-species">Fishing pressure rewired a species</h2>



According to researchers from <a href="https://www.geomar.de/en/">GEOMAR Helmholtz Centre for Ocean Research Kiel</a>, decades of intense fishing pressure didn’t just reduce the population - it rewired the species itself. 



The new study shows that human actions have altered the actual genetic makeup of cod in the Baltic Sea.



“Selective overexploitation has altered the genome of Eastern Baltic cod,” explains Dr. Kwi Young Han, the study’s first author. “We see this in the significant decline in average size, which we could link to reduced growth rates." 



"For the first time in a fully marine species, we have provided evidence of evolutionary changes in the genomes of a <a href="https://www.earth.com/news/oceans-are-quickly-losing-ability-to-support-fish-due-to-plankton-loss/">fish population</a> subjected to intense exploitation, which has pushed the population to the brink of collapse.”



<h2 class="wp-block-heading" id="h-changes-in-cod-genetics">Changes in cod genetics</h2>



The study links specific genetic changes to a shift in how cod grow and reproduce. The researchers found that genetic variants tied to growth became more or less common over time - classic signs of what’s called directional selection. 



These variants weren’t random either. They matched up with known genes that influence size and reproduction.



The experts also observed changes in a particular section of the cod genome - a chromosomal inversion - that typically helps animals adapt to environmental stress. 



In this case, it followed the same <a href="https://www.earth.com/news/lifes-rules-natural-selection-change-significantly-often-daphnia/">selection</a> pattern, reinforcing that the shrinking of the cod isn’t just bad luck or poor diet. It’s evolution, triggered by how we fish.



<h2 class="wp-block-heading" id="h-dna-from-the-past">DNA from the past</h2>



To study this long-term shift, the team turned to something unusual: tiny stones in fish ears called otoliths. Like tree rings, they store growth data year by year. 



The scientists used 152 otolith samples collected from the Bornholm Basin between 1996 and 2019 - part of GEOMAR’s Baltic Sea Integrative Long-Term Data Series.



The researchers paired chemical analysis of the otoliths with high-resolution DNA sequencing. They traced how cod growth patterns and genetic traits shifted across nearly three decades of <a href="https://www.earth.com/news/the-hidden-consequences-of-catch-and-release-sport-fishing/">fishing pressure</a>.



<h2 class="wp-block-heading" id="h-evolution-driven-by-human-activity">Evolution driven by human activity</h2>



The outcome? Cod that grew fast and large used to be common. Now, they’ve nearly vanished. The survivors are the ones that grow slower, mature smaller, and escape early capture.



“When the largest individuals are consistently removed from the population over many years, smaller, faster-maturing fish gain an evolutionary advantage,” noted Dr. Thorsten Reusch, head of the Marine Ecology Research Division at GEOMAR. 



“What we are observing is <a href="https://www.earth.com/news/fish-evolution-takes-place-in-decades-not-millions-of-years/">evolution</a> in action, driven by human activity. This is scientifically fascinating, but ecologically deeply concerning.”



<h2 class="wp-block-heading" id="h-cod-recovery-isn-t-guaranteed">Cod recovery isn’t guaranteed</h2>



The genetic changes found in cod aren't easily reversible. Cod that grow slowly and reproduce early might be surviving, but they’re also less productive. They mature at smaller sizes and produce fewer offspring. 



Furthermore, the genetic diversity of cod is shrinking. This diversity is crucial for helping species adapt to new conditions.



“Evolutionary change unfolds over many generations,” said Dr. Reusch. “Recovery takes far longer than decline, and it may not even be possible. This is evident in our 2025 length data from the current ALKOR cruise: despite the fishing ban, there’s no sign of a rebound in body size.”



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



This isn’t just about fish. It’s about how quickly humans can push a species to evolve in real time - and how hard it is to undo that. Genetic changes don’t bounce back when the pressure’s off. They linger, and in many cases, they stick.



“Our results demonstrate the profound impact of human activities on wild populations, even at the level of their DNA,” said Dr. Han. “They also highlight that sustainable <a href="https://www.earth.com/news/bleaching-effect-coral-loss-threatens-fisheries-and-livelihoods/">fisheries</a> are not only an economic issue, but also a matter of conserving biodiversity, including genetic resources.”



The science is clear. Overfishing doesn’t just take fish out of the sea. It leaves a permanent mark on the species. And it might have already cost us more than we can get back.



The full study was published in the journal Science Advances.



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Humans have changed the genetic makeup of cod

Cod once ruled the Baltic Sea - massive, plentiful, and...

Plateosaurus,Couple,,Dinosaurs,From,The,Late,Triassic,Period,Walking,On

Every visitor to the Natural History Museum in Zurich is greeted by a massive dinosaur skeleton nicknamed “Teoplati.” At first glance, it looks like any other prehistoric fossil on display, except for the presence of a serious bone infection. 



Teoplati’s story is anything but ordinary. 



This eight-meter Plateosaurus, which lived 220 million years ago in what is now Switzerland, met its end in sticky mud - and researchers say it was already struggling long before that. The dinosaur’s right arm, it turns out, was badly infected.



Scientists from the <a href="https://www.uzh.ch/en.html" target="_blank" rel="noreferrer noopener">University of Zurich</a>, along with researchers at the Frick Dinosaur Museum, recently studied the fossil and uncovered one of the oldest - and most severe - cases of bone infection ever recorded in a dinosaur.



<h2 class="wp-block-heading" id="h-mud-bound-dinosaur-had-a-useless-arm">Mud-bound dinosaur had a useless arm</h2>



Back in the <a href="https://www.earth.com/news/africas-oldest-known-dinosaur-recently-discovered/">Late Triassic </a>epoch, the Frick Valley in Aargau was a flat, dry landscape prone to sudden flooding. 



Picture a massive clay pit in a semi-arid basin - perfect for trapping large animals like Plateosaurus. Many of these dinosaurs likely died the same way: caught in the mud with no way out.



But this particular <a href="https://www.earth.com/news/scientists-discover-a-33-foot-jurassic-giant-twice-as-big-as-its-cousin-xingxiulong/">Plateosaurus</a> had even worse odds. It was already injured.



The dinosaur’s right shoulder and upper arm were severely damaged by a chronic infection. 



When researchers examined the bones, they found signs of intense inflammation and deformation - evidence that the animal’s limb had been unusable long before it became stuck in the mud.



<h2 class="wp-block-heading" id="h-ct-scanners-detect-dinosaur-bone-infection">CT scanners detect dinosaur bone infection</h2>



The nearly complete skeleton was unearthed in 2018. Paleontologists from the University of Zurich began studying it closely, especially the damaged limb. 



To get a better look inside, they used high-tech CT scanners at Empa, the Swiss Federal Laboratories for Materials Science and Technology.



These scanners, typically used for industrial research, were the only machines large enough to handle the dinosaur’s massive bones.



What they found was striking. The Plateosaurus likely suffered from <a href="https://www.earth.com/news/bone-disease-killed-off-australias-giant-thunder-birds/">osteomyelitis</a> - a serious infection that attacks bone tissue.



<h2 class="wp-block-heading" id="h-osteomyelitis-is-still-common-today">Osteomyelitis is still common today</h2>



"Osteomyelitis affects many living animals, including <a href="https://www.earth.com/news/evolutionary-mystery-why-are-mammals-the-only-vertebrates-to-have-only-one-lower-jawbone/">mammals</a> such as humans, as well as birds and reptiles," explained Jordan Bestwick, postdoctoral fellow at the Department of Paleontology at UZH.



"This disease is known to have affected several different dinosaur groups, including <a href="https://www.earth.com/news/giant-sauropods-walked-more-like-hippos-than-elephants/">sauropods</a>, so we had access to a range of specimens to compare our Plateosaurus with." said Bestwick.



"The affected bones in the shoulder and upper arm have unusually rough internal and external textures, altered shapes, and are even fused together - symptoms that are broadly typical of osteomyelitis."



What makes this case so unique is the size of the infected area. 



"Previous studies of osteomyelitis in dinosaurs report localized areas of infection, such as toe bones or a couple of adjacent bones in the spine," explained Bestwick.



"Having an entire infected shoulder and upper arm is very unusual. Although we don't know what initially caused the infection, the animal likely suffered from this disease for a substantial part of its life, possibly rendering its right arm useless."



<h2 class="wp-block-heading" id="h-jurassic-infection-links-dinosaurs-and-humans">Jurassic infection links dinosaurs and humans</h2>



Today, Teoplati stands tall at the entrance of the Natural History Museum at the University of Zurich. 



The skeleton lies in the exact position in which it was found. Next to it stands a life-sized reconstruction that shows what the animal may have looked like in life - including the deformed right arm.



Dennis Hansen, who led the exhibit’s creation at the museum, said the display tells more than just a biological story - it’s a personal one. "We wanted a display that highlights the tragic story of this particular animal," said Hansen.



The exhibit includes a diorama of cracked mud and footprints - some of the dinosaur’s last steps - before it sank beneath the surface.



"Together with the paleo-reconstruction wizards from the Danish company 10 Tons, we created a reconstruction based on the skeleton that also showcases the disease on its right arm and shoulder," said Hansen.



"This makes the display one of the few, worldwide, where the reconstruction of an individual dinosaur includes its pathologies."



In other words, it’s not just a dinosaur. It’s a story of injury, survival, and an unlucky end. Visitors walking into the museum aren’t just meeting an ancient creature - they’re meeting an individual with a history written in its bones.



The full study was published in the journal <a href="https://sjpp.springeropen.com/articles/10.1186/s13358-025-00368-3">Swiss Journal of Palaeontology</a>.



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220-million-year-old Plateosaurus dinosaur died from a crippling bone infection

Every visitor to the Natural History Museum in Zurich is...

Bluebottles - also known as Portuguese man o' war - are jellyfish-like marine creatures with long, stinging tentacles that often wash up on beaches. It's been widely assumed that bluebottles all belong to a single species, but a new global genetic survey has revealed otherwise.



Dr. Samuel H. Church of <a href="https://www.yale.edu/" target="_blank" rel="noreferrer noopener">Yale University</a> coordinated the genome work with Australian colleagues, including Professor Kylie Pitt from Griffith University. Their findings overturn two centuries of scientific classification.



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



The Portuguese man o’ war (Physalia physalis is the main species name), also known as the bluebottle, is a siphonophore - not a <a href="https://www.earth.com/news/world-jellyfish-day-2024-protecting-the-health-of-our-oceans/">true jellyfish</a>, although it closely resembles one. 



What makes it extraordinary is that it’s not a single organism but a colonial one - comprised of genetically identical individuals called zooids. 



Each zooid performs a specialized role: one floats, another captures prey with stinging tentacles, a third digests, and yet another reproduces. 



These zooids function together as if they were one being, demonstrating a remarkable example of biological division of labor and cooperative survival.



This organism’s iconic translucent float, or <a href="https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/pneumatophores" target="_blank" rel="noreferrer noopener">pneumatophore</a>, sits atop the water like a small sail, catching the wind to move it across the ocean’s surface. 



Beneath it trail long, venomous tentacles - sometimes over 30 feet - that contain specialized cells called nematocysts, which fire harpoon-like structures to inject potent venom into prey. 



Despite its beauty, the sting can be extremely painful to humans and potentially dangerous, though rarely fatal. The man o’ war plays a critical ecological role in <a href="https://www.earth.com/news/how-the-sharks-body-grows-with-geometric-precision/">pelagic food webs</a>, preying on small fish and plankton while serving as food for predators like the blanket octopus and loggerhead turtle.



<h2 class="wp-block-heading" id="h-four-species-of-bluebottles">Four species of bluebottles</h2>



The team sorted the <a href="https://oceanservice.noaa.gov/facts/portuguese-man-o-war.html" target="_blank" rel="noreferrer noopener">specimens</a> into Physalia physalis, P. utriculus, P. megalista, and a newly named Physalia minuta, the last discovered in waters south of New Zealand. Each species carries distinctive sail colors and float shapes - traits once dismissed as harmless variation.



Genetic markers show the four <a href="https://www.earth.com/news/world-jellyfish-day-2024-protecting-the-health-of-our-oceans/">lineages</a> do not interbreed, even when they occupy the same stretch of ocean. This pattern means evolution is at work in the open sea, not only along coastlines or around islands.



“We were shocked, because we assumed they were all the same species,” said Professor Pitt. Her remark echoes a long‑held textbook view now overturned.



Every colony is a <a href="https://twilightzone.whoi.edu/explore-the-otz/creature-features/siphonophore/" target="_blank" rel="noreferrer noopener">siphonophore</a> - a floating commune of genetically identical zooids that act as one animal. The arrangement lets a bluebottle grow long feeding tentacles while the gas‑filled float keeps the colony at the surface, a lifestyle that defines the <a href="https://theoceancleanup.com/updates/neuston-in-the-great-pacific-garbage-patch-and-the-impact-of-cleanup/" target="_blank" rel="noreferrer noopener">neuston</a> layer.



<h2 class="wp-block-heading" id="h-differences-beyond-appearance">Differences beyond appearance</h2>



Raw genomes alone rarely hint at an animal’s appearance, so the researchers combed through 4,000 beach photographs. Color signatures and sail angles in the pictures matched the genetic <a href="https://www.earth.com/news/giant-phantom-jelly-discovered-exposed-ecosystem-under-antarctic-iceberg/">lineages</a> one by one.



Citizen scientists had, in effect, been taking field notes for years without knowing it. Their uploads supplied location data that helped map where each species turns up during different wind seasons. 



Machine‑learning tools flagged subtle differences, such as a deep‑purple crest on P. megalista or the small, clear float on P. minuta. Laboratory vouchers later verified those traits under a microscope.



The public photo trove also clarified left‑handed versus right‑handed sails, a feature that decides which way a bluebottle is blown. Such handedness now appears tied to species identity rather than simple developmental chance.



<h2 class="wp-block-heading" id="h-ocean-currents-separate-bluebottle-species">Ocean currents separate bluebottle species</h2>



<a href="https://www.earth.com/news/jellyfish-more-than-just-a-snack-for-predatory-fish/">Ocean</a> circulation models recreated likely drift paths from hatchling to adult, revealing corridors that keep populations apart. 



Prevailing winds in the Pacific sweep P. utriculus west toward Australia, while the South Equatorial Current loops P. megalista into the Atlantic. 



The new species, P. minuta, hugs eddies of the <a href="https://www.sciencedirect.com/science/article/abs/pii/S0924796319300259" target="_blank" rel="noreferrer noopener">Tasman Front</a>, a route that spirals larvae southward before they ever cross open ocean. Because gonads detach and sink below the surface to spawn, deep water layers also partition gene flow.



Subtle climate shifts could shuffle these corridors and mix the species in the future, but for now the lines stay crisp. That stability gives evolutionary forces room to sculpt body size, venom genes, and reproductive timing without interference. 



The finding challenges a common idea that wind‑powered drifters form one gigantic, well‑mixed population. Instead, even a creature built for travel can remain genetically provincial.



<h2 class="wp-block-heading" id="h-bluebottle-stings-vary-by-species">Bluebottle stings vary by species</h2>



<a href="https://sls.com.au/bluebottlewatch-a-new-research-project-to-develop-a-bluebottle-prediction-tool-for-our-beaches/" target="_blank" rel="noreferrer noopener">Surf Life Saving Australia</a> ranks bluebottle contact as a leading reason for first‑aid calls, spurring a research grant to build a beach sting forecast. 



Knowing which species is likely to arrive could sharpen those alerts, because tentacle length and venom chemistry differ among the four.



During the summer of 2017, more than <a href="https://www.abc.net.au/news/2017-03-01/bluebottle-stings-up-900-per-cent-in-queensland/8313970" target="_blank" rel="noreferrer noopener">38,000 people</a> were treated for bluebottle stings in Queensland alone - a spike of 900 percent over the prior season. 



<h2 class="wp-block-heading" id="h-forecasting-bluebottle-seasons">Forecasting bluebottle seasons</h2>



Public health planners can now add species identity to their toolbox instead of relying on wind direction alone.



Lighter winds often carry the smaller P. minuta onto sheltered south‑facing bays, where novice swimmers gather. 



Lifeguards armed with species‑level forecasts might adjust patrols or signage accordingly. Thermal anomalies that favor jellyfish blooms may not boost every bluebottle equally, given their genetic split.



Future sting seasons could therefore hinge on which lineage catches the breeze rather than on sheer water temperature.



<h2 class="wp-block-heading" id="h-hidden-population-structure-in-the-ocean">Hidden population structure in the ocean </h2>



The bluebottle story joins other case studies of copepods and pteropods that show hidden population structure in the high seas. 



Collectively, these results overturn the old axiom that “everything is everywhere” once an organism can drift. Marine cleanup projects often claim surface life is sparse, implying little ecological risk when skimming plastics. 



Evidence of partitioned diversity urges far more caution before nets sweep across convergence zones.



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



Pharmaceutical scouts have isolated novel peptide toxins from P. physalis, but untapped species may hold different compounds with medical promise. A four‑species framework sets a clearer path for bioprospecting teams.&nbsp;



Climate models aiming to forecast <a href="https://www.earth.com/news/marine-robots-are-exploring-the-oceans-role-in-climate-control/">oceanic carbon</a> cycling need accurate species counts because each colony’s buoyant gas is nearly 13 percent carbon monoxide. Four distinct production rates could alter estimates of gas exchange at the air–sea interface.



Researchers who track long‑range migrants, from sea turtles to seabirds, can now refine diet studies. Predator scat may tell which bluebottle species dominates a given flyway, adding another layer to ecosystem maps.



<h2 class="wp-block-heading" id="h-toxin-genes-in-bluebottle-species">Toxin genes in bluebottle species </h2>



Work is already under way to test whether the four lineages differ in toxin genes, an angle that could explain regional differences in sting severity. 



Another puzzle lies in the handedness trait, which might be hardwired by alleles rather than molded by early winds.



Field biologists plan to tag floats with tiny temperature loggers to see how much time each species spends in sun‑baked surface water. Results should reveal whether thermal tolerance helped split the lineages in the first place.



The study is published in the journal <a href="https://www.cell.com/current-biology/abstract/S0960-9822(25)00682-7" target="_blank" rel="noreferrer noopener">Current Biology</a>.



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Biologists discover that the "Portuguese man o' war" has multiple species

Bluebottles - also known as Portuguese man o' war -...

Child-directed speech, also known as “baby talk,” plays a vital role in human development. Around the world, caregivers use a distinct vocal style to talk to infants. 



These modified speech patterns help young minds absorb vocabulary and structure. But how did this behavior originate? Could it have evolved from our primate ancestors?



A recent study led by researchers from the <a href="https://www.uzh.ch/en.html" target="_blank" rel="noreferrer noopener">University of Zurich</a>, <a href="https://www.unine.ch" target="_blank" rel="noreferrer noopener">University of Neuchâtel</a>, and collaborators across Europe and the U.S. offers new insights. 



The research, published in the journal Science Advances, explores whether great apes use infant-directed vocalizations like humans do.



<h2 class="wp-block-heading" id="h-baby-talk-in-humans-and-apes">Baby talk in humans and apes</h2>



The team observed wild populations of bonobos, chimpanzees, gorillas, and orangutans. They also included data from human infants across diverse cultures: Shipibo-Konibo, Qaqet, Chintang, and Tuatschin.



To quantify communication, they analyzed vocal behavior during two-minute intervals. They categorized each instance as infant-directed, surrounding, or general vocal activity. 



They followed immature individuals closely, noting all relevant sounds from nearby group members.



<h2 class="wp-block-heading" id="h-humans-use-baby-talk-way-more">Humans use baby talk way more</h2>



These results highlight how unique human caregiving behavior is compared to that of our closest relatives. Human <a href="https://www.earth.com/news/how-do-infants-connect-with-the-world-it-all-starts-with-the-feet/">infants</a> are surrounded by vocal input that is not only frequent but also specifically tailored to them. This level of attention likely helps them learn language faster and more efficiently.



Even when focusing only on what mothers said, humans stood out. Mothers spoke directly to their babies far more than ape mothers did. In fact, the difference between human and bonobo mothers was over 400-fold.



Most of the speech around human infants was directed at them. In contrast, great apes showed almost no such targeted communication. 



This suggests that humans may have evolved a special way of teaching language that relies heavily on speaking directly to infants.



<h2 class="wp-block-heading" id="h-not-just-direct-speech">Not just direct speech</h2>



Surrounding speech refers to vocalizations that infants can hear but are not directly addressed to them. This type of input was fairly consistent across humans, <a href="https://www.earth.com/news/chimpanzees-select-the-best-materials-for-termite-fishing/">chimpanzees</a>, and bonobos. 



These species likely live in more socially active environments, where infants overhear conversations or calls.



Orangutans, however, received much less surrounding speech. This fits their more solitary lifestyle, where fewer individuals are nearby to produce vocalizations.



Because infant-directed speech is rare among apes, they may depend more on what they hear in the background. This ambient input could help them learn communication patterns, even without being directly taught.



<h2 class="wp-block-heading" id="h-baby-talk-helped-humans-evolve">Baby talk helped humans evolve</h2>



The data suggest a sharp evolutionary shift. “Our findings suggest that the tendency to direct vocalizations at infants... has been massively expanded in the human lineage,” the authors wrote.



One possible driver is the need to transmit learned communication. Unlike apes, human language is highly flexible and requires teaching. Infant-directed speech helps children grasp words, tone, and context more easily.



Interestingly, gestures may play a more prominent role in great apes. Repetitive <a href="https://www.earth.com/news/wild-bird-uses-wing-gestures-to-politely-say-after-you/">gestures</a> in apes mirror some features of human baby talk. These findings hint that vocal and gestural teaching modes may have evolved in parallel.



<h2 class="wp-block-heading" id="h-are-humans-alone-not-quite">Are humans alone? Not quite</h2>



Other species also engage in infant-directed communication. Dolphins change pitch when around calves. Bats alter calls to suit pups. Cats and monkeys use specific sounds to call or calm infants.



However, these communications likely serve different functions, like identification or retrieval. Only in humans do these vocal patterns appear tightly linked to complex language learning.



<h2 class="wp-block-heading" id="h-studying-apes-to-understand-ourselves">Studying apes to understand ourselves</h2>



The study opens up new paths. The researchers propose exploring who produces surrounding speech in ape societies, siblings, mothers, or others, and whether that affects learning.



Additionally, they call for deeper study of ape gestures directed at infants. “The gestural modality might represent an additional fruitful avenue for future work."



This research provides strong support that child-directed speech may have evolved to support <a href="https://www.earth.com/news/babies-can-naturally-learn-multiple-languages-from-birth/">language learning</a>. Our ancestors likely began with ambient communication, then shifted toward more intentional, tailored speech as language grew more complex.



By comparing the way species talk, or don’t talk, to their young, we gain a clearer view of what makes human language so powerful and so unique.



The study is published in the journal <a href="https://www.science.org/doi/10.1126/sciadv.adt7718" target="_blank" rel="noreferrer noopener">Science Advances</a>.



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Baby talk may explain what sets humans apart from apes

Child-directed speech, also known as “baby talk,” plays a vital...

The monarch may steal the spotlight, yet an ongoing crisis is affecting nearly every butterfly <a href="https://www.earth.com/news/butterflies-can-adapt-quickly-but-evolution-has-its-limits/">species</a> in the lower 48. Between 2000 and 2020, total abundance fell by 22 percent, according to the largest survey ever assembled.



That national <a href="https://naba.org/wp-content/uploads/2025/03/Rapid-butterfly-declines-across-the-United-States-during-the-21st-century_Science_03072025.pdf" target="_blank" rel="noreferrer noopener">dip</a> works out to 1.3 percent each year, a slow‑motion slide that rarely makes headlines but never takes a day off.



<h2 class="wp-block-heading" id="h-butterfly-species-decline-and-habitat-loss">Butterfly species decline and habitat loss</h2>



Roughly a third of the 342 <a href="https://www.earth.com/news/butterfly-migration-habits-are-not-determined-by-their-dna/">species</a> with solid data are shrinking fast, and 107 have already slipped by more than half of their former counts. 



Habitat carved into parking lots, hotter summers driven by climate change, and heavy use of pesticides each gnaw at different life stages, yet together they form a three‑pronged squeeze.



Even the unglamorous caterpillar matters here: without the right host leaves, no egg survives, no adult emerges, and no pollination happens. 



Cheryl Schultz of <a href="https://wsu.edu/">Washington State University</a> helped write the new recovery roadmap. She says the clock is ticking for the insects she has studied for three decades.



<h2 class="wp-block-heading" id="h-long-term-drop-in-butterfly-numbers">Long-term drop in butterfly numbers</h2>



The Science team pulled 12.6 million field observations from 76,000 surveys, then wrangled conflicting protocols into one set of trend lines.



Patterns varied by region, but the Southwest stood out as hardest hit, while the Pacific Northwest held steady only because one irruptive tortoiseshell species briefly boomed.



The authors stress that <a href="https://www.earth.com/news/butterfly-hovering-technique-could-revolutionize-drone-design/">butterflies</a> act as living barometers: when they vanish, so do many less‑monitored insects doing similar ecological work. 



Losing butterflies also removes food for birds and other wildlife that depend on soft‑bodied prey each spring.



<h2 class="wp-block-heading" id="h-cleaning-data-to-track-real-trends">Cleaning data to track real trends</h2>



Tracking butterfly abundance across hundreds of species isn't easy. Observations often come from community science platforms like iNaturalist, where users sometimes upload misidentified species or report tropical butterflies from butterfly houses as wild sightings.



To clean the data, researchers used <a href="https://txtav.com/en/range-map" target="_blank" rel="noreferrer noopener">range maps</a> to flag out-of-place records and exclude bad data from their models. 



Eliza Grames, an assistant professor at <a href="https://www.binghamton.edu/">Binghamton University</a>, said this step was key to making sure the trends reflected actual changes in nature rather than errors in reporting. Professor Grames specializes in using <a href="https://libguides.uta.edu/quantitative_and_qualitative_research/quant" target="_blank" rel="noreferrer noopener">quantitative methods</a>, evidence synthesis, and long-term datasets to understand how climate, habitat loss, and species interactions are affecting biodiversity. 



Her work focuses on combining scattered data sources like historical surveys and citizen science to track insect declines and guide effective conservation.



<h2 class="wp-block-heading" id="h-restoring-habitats-for-butterfly-species">Restoring habitats for butterfly species</h2>



Scott Black is the director of the <a href="https://www.xerces.org/">Xerces Society</a> and a co‑author of the recovery roadmap.



"Butterflies need host plants on which to lay eggs, wildflowers on which to feed, a refuge from pesticides, and sites to overwinter. There is hope for these animals if we focus on providing habitat for butterflies across all landscapes,” said Black. 



Providing season‑long bloom is key, and <a href="https://xerces.org/pollinator-conservation/habitat-restoration/management" target="_blank" rel="noreferrer noopener">Xerces</a> maintains region‑specific plant lists that match native flowers with local nectar feeders.



Land managers are urged to skip blanket spraying and instead spot‑treat weeds, mow outside bloom windows, and leave leaf litter for overwintering adults or chrysalids. 



Protecting habitat also buffers butterflies against flash droughts and early frosts that are becoming more common as weather swings widen.



<h2 class="wp-block-heading" id="h-green-spaces-support-butterfly-species">Green spaces support butterfly species</h2>



The recovery roadmap emphasizes that conservation must happen everywhere, not just in protected wilderness. Even small green spaces can play a huge role when stitched together across cities, suburbs, and farms.



Pollinator corridors, like roadside flower strips or native plant buffers on farmland, let butterflies travel, feed, and lay eggs without interruption. 



When neighbors and land managers coordinate efforts, isolated patches of habitat can become a functioning network that supports entire species.



<h2 class="wp-block-heading" id="h-butterfly-species-and-cotton-yields">Butterfly species and cotton yields</h2>



Economics add weight to conservation: research in <a href="https://cns.utexas.edu/news/research/supporting-pollinators-could-have-big-payoff-texas-cotton-farmers" target="_blank" rel="noreferrer noopener">Texas</a> shows that <a href="https://www.earth.com/news/national-learn-about-butterflies-day-an-enchanting-world-awaits/">butterflies</a> translate into about $100 million in annual pollination value for cotton alone.



When rows of nectar plants bordered the fields, cotton set more bolls, and farmers noticed a boost in yield without another drop of chemical inputs.



<h2 class="wp-block-heading" id="h-how-to-help-butterfly-species">How to help butterfly species</h2>



Homeowners can swap a slice of turf for milkweed, asters, and goldenrod. City planners can seed bloom strips along bike paths and medians instead of short mowed grass.



Rural roadsides double as corridors when mowing heights stay above six inches and herbicide use is limited to targeted patches, a change that costs little but scales quickly.



Even small pollinator islands in solar arrays or utility rights‑of‑way create stepping‑stones that let populations recolonize after drought or fire.



Success stories already exist. The Fender’s blue butterfly, once presumed lost, bounced back enough for the <a href="https://oregoncapitalchronicle.com/2023/10/16/pink-wildflower-in-oregon-and-southwest-washington-removed-from-federal-protection/" target="_blank" rel="noreferrer noopener">U.S. Fish &amp; Wildlife Service</a> to reclassify it from endangered to threatened in 2023.



The study is published in the journal <a href="https://www.science.org/doi/10.1126/science.adp4671" target="_blank" rel="noreferrer noopener">Science</a>.



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Butterfly species are declining fast across the United States

The monarch may steal the spotlight, yet an ongoing crisis...

Relocating elephants to fresh herds can boost genetics and social health - but what if the animals can’t “talk” to their new hosts? 



Field biologists have discovered that elephant groups separated by only a few hundred miles emit subtly different low-frequency rumbles. Those dialects might complicate friendships, alliances, or alarm calls when animals are translocated. 



The puzzle is part of a broader realization that many species possess local traditions - learned behaviors that function much like human culture.



To help researchers explore that idea, scientists at the <a href="https://www.arizona.edu/">University of Arizona</a> have launched the first open-access, global catalog of animal <a href="https://www.earth.com/news/saving-the-cultural-legacy-of-wild-animals/">cultures</a>.



<h2 class="wp-block-heading" id="h-mapping-animal-cultures">Mapping animal cultures</h2>



The <a href="https://viz.datascience.arizona.edu/ACDB/">Animal Culture Database</a> brings together hundreds of peer-reviewed reports on socially learned behaviors - from whales’ evolving migration routes to chimpanzees’ stone-tool know-how.



Kiran Basava is the paper’s lead author and a postdoctoral research associate at the University of Arizona.



“There is a consensus among animal behavior researchers that cultural traditions and socially learned behaviors are important to conservation,” said Basava. "There are decades of research investigating these behaviors across different species that are scattered throughout the literature."



"We synthesized that work to facilitate creative research and discussions about how culture is defined across different species, as well as how animals respond to different environmental disturbances caused by humans.”



<h2 class="wp-block-heading" id="h-animal-culture-by-region">Animal culture by region</h2>



The database centers on an interactive world map dotted with pins. Click on a marker and you can read about orangutans’ nesting tricks in Borneo, humpback <a href="https://www.earth.com/news/hidden-patterns-in-whale-songs-predict-ecosystem-shifts/">whales</a>’ complex songs off Tonga, or urban crows that drop nuts at traffic lights so cars will crack them open.



A search panel lets visitors filter by species, behavior type, or geographic region. For example, it reveals how rats in European forests learned to peel pinecones, or how certain <a href="https://www.earth.com/news/some-birds-trick-their-way-into-mating-by-removing-testosterone-from-their-bodies/">birds</a> remodeled mating dances after wildfires changed their habitat.



<h2 class="wp-block-heading" id="h-building-a-living-archive">Building a living archive</h2>



To assemble the resource, Basava and colleagues combed through thousands of journal articles published over several decades. 



The experts screened more than 1,000 promising papers. From those, they coded 121 into the pilot version - covering 30 mammalian, 30 avian, and one insect species. The team is adding 600 more studies and will soon let other scientists upload their own findings.



Study co-author Cristian Román-Palacios, an assistant professor of information science, said the tool could transform how researchers study cultural evolution.



“You can investigate the origins of culture by not just tracing it back to humans, but by seeing how much variance there is between different species and asking what drives those differences,” explained Professor Román-Palacios.



“Culture is not just a human phenomenon, and this database can help investigate what drives culture across the animal kingdom.”



<h2 class="wp-block-heading" id="h-cultural-loss-risks-extinction">Cultural loss risks extinction</h2>



Understanding animal culture is more than academic curiosity. Conservationists are realizing that an <a href="https://www.earth.com/news/elephants-may-be-the-first-non-human-animals-to-call-each-other-by-names/">elephant dialect</a>, a whale migration route, or a songbird melody can be as crucial as genetics for a population’s survival.



Human-driven habitat loss, noise pollution, and climate change threaten to erase those traditions. If relocated elephants cannot communicate with resident herds, or if dam construction blocks a salmon run taught across generations, restoration projects may fail.



By pooling case studies in one searchable hub, the database helps practitioners identify culturally important behaviors that need protection - much like <a href="https://www.unesco.org/en">UNESCO</a>’s list of human cultural heritage.



The data can also reveal patterns: Are populations with richer cultural repertoires more resilient to disturbance? Do species that lose key traditions decline faster?



<h2 class="wp-block-heading" id="h-science-meets-animal-tradition">Science meets animal tradition</h2>



The experts hope educators will use the site to teach evolutionary biology, while data scientists mine the entries for global trends. Basava envisions adding tools to visualize how behaviors spread over time, akin to epidemiological models for disease.



Future iterations may incorporate audio clips of vocalizations or video of <a href="https://www.earth.com/news/some-fish-use-tools-to-crack-open-prey/">tool use</a>, creating a multimedia atlas of animal ingenuity. 



The designers also plan multilingual interfaces to attract contributions from researchers worldwide, including Indigenous observers whose knowledge often predates academic studies.



<h2 class="wp-block-heading" id="h-culture-isn-t-just-human">Culture isn’t just human</h2>



The project resonates with a paradigm shift in biology: culture is no longer viewed as uniquely human. 



From dolphins that pass down signature whistles to capuchin monkeys that adopt local grooming fashions, <a href="https://www.earth.com/news/food-availability-influences-social-learning-among-orangutans/">social learning</a> pervades the animal kingdom. Recognizing those parallels can inform debates about animal welfare and cognitive rights, the authors note.



And it may reshape how humans see ourselves. If elephants currently need a translator, perhaps conservation must consider not just where animals live. It should also account for how they live - their languages, crafts, and customs forged over millennia.



For now, the Animal Culture Database offers anyone with an internet connection a front-row seat to those hidden worlds. The database preserves animal-taught traditions and reminds us that culture extends beyond just the human species.



The study is published in the journal <a href="https://www.nature.com/articles/s41597-025-05315-y">Nature Scientific Data</a>.



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From rumbles to rituals: Scientists map the cultures of the animal kingdom

Relocating elephants to fresh herds can boost genetics and social...

Bird species add color, movement, and sound to our world. They pollinate plants, control pests, and spread seeds. But their future is in danger.



A new study from the <a href="https://www.reading.ac.uk" target="_blank" rel="noreferrer noopener">University of Reading</a> warns that climate change and habitat destruction threaten global bird diversity. 



The loss of unique birds like the bare-necked umbrellabird, helmeted hornbill, and yellow-bellied sunbird-asity would shrink the variety of bird forms that support <a href="https://www.earth.com/news/big-brains-and-wide-ranges-cant-save-birds-from-climate-change/">ecosystems</a>.



This projection triples all recorded bird extinctions since 1500 CE. Even with protection from hunting, habitat loss, and climate change, 250 species may still disappear. Some birds are now too fragile to survive without direct help.



“Many birds are already so threatened that reducing human impacts alone won't save them. These species need special recovery programs, like breeding projects and habitat restoration, to survive,” explained Kerry Stewart, lead author of the study.



“We face a bird extinction <a href="https://www.earth.com/news/birds-are-struggling-to-keep-pace-with-a-warming-climate/">crisis</a> unprecedented in modern times. We need immediate action to reduce human threats across habitats and targeted rescue programs for the most unique and endangered species.”



<h2 class="wp-block-heading" id="h-large-bird-species-are-most-at-risk">Large bird species are most at risk</h2>



The researchers studied nearly 10,000 bird species using IUCN Red List data and advanced models. 



The results showed that large-bodied birds are especially at risk. These birds struggle more with hunting pressure and climate stress. Birds with broad wings face severe danger from habitat destruction, especially in forests.



The study went beyond just species counts. It measured the expected loss of “functional diversity,” a term describing the variety of bird shapes, diets, and behaviors. 



Under current trends, global bird functional diversity could fall by about 3.2% in the next 100 years. This drop may sound small, but it would seriously damage ecosystems. 



Large, distinct <a href="https://www.earth.com/news/bird-evolution-timeline-pushed-back-20-million-years-by-baminornis-zhenghensis-discovery/">species</a> often provide unique services. Their disappearance would leave functional gaps that smaller or similar birds cannot fill.



<h2 class="wp-block-heading" id="h-limits-of-protection-alone">Limits of protection alone</h2>



The researchers tested three future scenarios: complete, partial, and minimal threat abatement. In the best case, where all human threats were removed across species ranges, around 250 species would still go extinct. That is nearly half of all projected losses, even with ideal conservation.



Some birds, like the Cebu flowerpecker, remain highly vulnerable despite facing few listed threats. With fewer than 70 individuals left, they may vanish without specific recovery steps like habitat restoration or captive breeding.



The study shows that reducing threats is not enough. Many species are already too close to the brink. Past damage, small populations, and isolated habitats all contribute to ongoing <a href="https://www.earth.com/news/birds-are-molting-earlier-in-the-fall-as-seasons-shift/">risks</a>.



<h2 class="wp-block-heading" id="h-threats-to-rare-bird-species">Threats to rare bird species</h2>



The research evaluated six main threats: habitat loss, hunting, climate change, invasive species, disturbance, and pollution. 



Habitat loss contributed the most to species decline, affecting over 1,600 species. Yet when it comes to preserving unique bird traits, other threats matter more.



Driver-specific results showed that reducing hunting or accidental deaths helped conserve rare bird features more effectively, even if fewer total species were saved. That means some threats disproportionately affect birds with uncommon traits.



Birds with long tails and short beaks, for example, benefited more from reduced hunting. Birds with broad wings responded better to protection from habitat destruction. These patterns help tailor conservation actions to bird traits most at risk.



<h2 class="wp-block-heading" id="h-strategic-recovery-of-unique-species">Strategic recovery of unique species</h2>



One solution stood out: target the most unique birds for rescue. The researchers created a list of 200 functionally unique species. Protecting just the top 100 could conserve over two-thirds of global bird functional diversity.



These birds include nectar-feeders, scavengers, and seed dispersers. From the Sulu hornbill to the southern royal albatross, many are island-dwelling, wide-ranging, or limited to one location. They carry traits that help regulate temperature, shape ecosystems, and fill rare ecological roles.



Preventing the extinction of around 37 of these birds could achieve this 68% protection goal. Since past efforts have already saved 21 to 32 bird species since 1993, this new goal appears feasible with commitment.



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



Even in optimistic futures, threats cannot be erased quickly or completely. Species recovery programmes, including in-situ and ex-situ measures, are needed for the most vulnerable.



“Stopping threats is not enough,” said Professor Manuela Gonzalez-Suarez. “Prioritizing conservation programs for just 100 of the most unusual threatened birds could save 68% of the variety in bird shapes and sizes. This approach could help to keep ecosystems healthy.”



Habitat protection remains key. But to safeguard ecosystem resilience, conservationists must also think about functional diversity, not just species counts.



The coming century will test humanity’s will to preserve Earth's avian legacy. Without sharp decisions and bold action, we risk losing many birds and the ecological balance they help maintain.



The study is published in the journal <a href="https://www.nature.com/articles/s41559-025-02746-z" target="_blank" rel="noreferrer noopener">Nature Ecology &amp; Evolution</a>.



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Hundreds of bird species could vanish in the next century

Bird species add color, movement, and sound to our world....

Anyone who has watched a cat sleep knows they do so with remarkable consistency. From curled tails to neatly tucked paws, their resting positions often seem almost ritual-like. But new research suggests the sleeping positions of cats are not just habits.



A global research team has found that most <a href="https://www.earth.com/news/cats-can-tell-people-apart-by-sniffing-them/">cats</a> prefer to sleep on their left side. By analyzing 408 YouTube videos, the researchers confirmed a significant bias toward this sleeping position. 



About 65% of the cats were seen resting with their left shoulder down, while only 35% chose the right side. "Sleeping on the left side can therefore be a survival strategy,” noted the researchers.



<h2 class="wp-block-heading" id="h-cats-sleep-left-to-react-faster">Cats sleep left to react faster</h2>



When a cat sleeps on its left, it wakes up using its left visual field. This field is processed in the brain’s right hemisphere, which handles spatial awareness, fear response, and fast movement coordination. 



“Asymmetries in behavior can have advantages because both hemispheres of the brain specialize in different tasks,” explained study co-author Onur Güntürkün.



Left-side sleeping allows cats to respond faster to threats from below or from the left. This sleep posture aligns with <a href="https://www.earth.com/news/international-lynx-day-2025-protecting-the-silent-hunters/">cats</a>’ tendency to rest in high places. 



Elevated locations limit predator access and provide better visibility. Combined with leftward sleeping, this may give cats a stronger edge when suddenly waking.



<h2 class="wp-block-heading" id="h-a-strong-left-side-bias">A strong left-side bias</h2>



The team examined only clear, unaltered videos showing single <a href="https://www.earth.com/news/how-and-why-do-cats-purr-scientists-finally-found-the-answers-genetic-dna/">cats</a> lying fully visible on one side for at least 10 seconds. Videos that were mirrored, low-resolution, or cropped were excluded. 



The results were statistically significant (χ² = 37.7, df = 1, p &lt; 0.001), showing a clear left-side preference.



This bias may not be random. It fits well with patterns seen in many species, where the right brain hemisphere plays a major role in detecting danger. 



Animals generally react faster to threats coming from their left side, suggesting an adaptive benefit to this positioning.



<h2 class="wp-block-heading" id="h-the-right-brain-helps-detect-danger">The right brain helps detect danger</h2>



“By specializing on one limb or one side of its sensory system, the contralateral hemisphere goes through life-long cycles of motor and perceptual learning,” wrote the study authors.



This helps speed up brain processing, cut down reaction times, and enhance accuracy. Sleeping with the left shoulder down lets the brain’s stronger threat-response side engage instantly when the cat awakens.



The right amygdala, which helps process fear, is more active in the right side of the brain. Since the right side also handles things like noticing space and spotting danger, this supports the idea that sleeping on one side may be linked to fear.



<h2 class="wp-block-heading" id="h-other-causes-for-cat-sleep-bias">Other causes for cat sleep bias</h2>



Could other factors influence sleep position? Maybe, but they are unlikely to change the overall pattern. For instance, pregnant cows lie on their left with moderate frequency. However, pregnancy rates alone cannot explain the strong leftward bias in this cat sample.



Another possible explanation is “pawedness,” preference for using one paw over the other. Around 78% of cats show some degree of paw preference. But left- and right-pawed cats occur in equal numbers. So paw dominance does not match the 65% left-sleeping pattern seen here.



Still, researchers caution that more studies are needed. The team had no access to sex or pregnancy data for the cats in the videos. But the strong population-level trend remains clear.



<h2 class="wp-block-heading" id="h-cats-sleep-habits-reveal-brain-evolution">Cats sleep habits reveal brain evolution</h2>



This finding adds to the growing evidence that cats, like many <a href="https://www.earth.com/news/cats-have-become-one-of-the-worlds-most-invasive-predators/">animals</a>, use subtle behavioral traits to stay safe. It also supports broader patterns of brain lateralization seen across mammals and birds.



The researchers believe these insights can help researchers understand how such asymmetries emerge. 



“Although this finding is subject to debate, it could provide an excellent opportunity to study the emergence of asymmetries at the population level,” they wrote.



For pet owners and scientists alike, this sleepy behavior may offer surprising clues about how brains and bodies work together to enhance survival and adaptation.



The study was led by researchers from the&nbsp;<a href="https://www.uniba.it/" target="_blank" rel="noreferrer noopener">University of Bari Aldo Moro</a>,&nbsp;<a href="http://www.ruhr-uni-bochum.de/en" target="_blank" rel="noreferrer noopener">Ruhr University Bochum</a>,&nbsp;<a href="https://www.medicalschool-hamburg.de/" target="_blank" rel="noreferrer noopener">Medical School Hamburg</a>, and other international partners.



The study is published in the journal <a href="https://www.cell.com/current-biology/fulltext/S0960-9822(25)00507-X" target="_blank" rel="noreferrer noopener">Current Biology</a>.



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Cats clearly prefer sleeping on their left side, here's why

Anyone who has watched a cat sleep knows they do...

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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

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

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

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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

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

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



<h2 class="wp-block-heading" id="h-ants-may-detect-other-pests-like-lanternflies">Ants may detect other pests like lanternflies</h2>



The method could be expanded to track other pests. Many <a href="https://www.earth.com/news/how-many-ants-live-on-earth-at-any-point-in-time-total-number-is-astounding/">insects</a> excrete honeydew, and ants can pick up their DNA too. This opens the door for broader pest detection strategies using the same principle.



Ants, in their natural role as sugar hunters, may become an essential part of protecting crops, forests, and native ecosystems. With antDNA, researchers are tapping into nature’s own behaviors to find smarter ways of monitoring invasive threats.



The study is published in the journal <a href="https://scijournals.onlinelibrary.wiley.com/doi/10.1002/ps.8814" target="_blank" rel="noreferrer noopener">NeoBiota</a>.



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How ants could help stop the tree-killing lanternfly

Virginia faces a stubborn enemy: the spotted lanternfly (SLF). These...

In the wild, social lives shape survival. For female chimpanzees, bonds with others aren't just emotional glue. They are critical for keeping babies alive. 



A new study of wild eastern chimpanzees in Gombe National Park finds that social integration predicts whether a newborn survives, even when no close kin is around.



<h2 class="wp-block-heading" id="h-chimpanzees-with-strong-social-bonds">Chimpanzees with strong social bonds</h2>



Female <a href="https://www.earth.com/news/laughter-lifts-bonobo-moods-offering-clues-to-human-emotion/">chimps</a> are often the ones who leave their birth group. That means most do not live near their mothers or sisters. Still, those who manage to build friendships with other females raise more babies to weaning age.



“In species where females live in groups with their sisters and mothers, it’s less surprising that female sociality is beneficial,” said <a href="https://scholars.duke.edu/person/joseph.feldblum" target="_blank" rel="noreferrer noopener">Joseph Feldblum</a>, lead author and research professor at Duke. 



“But female chimps don’t usually have that. They are also less gregarious than males, so the fact that forming strong social connections still matters is striking.”



<h2 class="wp-block-heading" id="h-babies-of-social-chimpanzees">Babies of social chimpanzees </h2>



The team analyzed 37 years of detailed records from 37 mothers and 110 offspring. Using a composite sociality index (CSI), they tracked how much time females spent associating or grooming others before giving birth.



Their best model showed that higher CSI scores, especially with other <a href="https://www.earth.com/news/baby-talk-may-explain-what-sets-humans-apart-from-apes/">females</a>, greatly increased infant survival to age one and even to age five. The effect held even after excluding mothers who died shortly after giving birth.



A female with a CSI score twice the average had a 95 percent chance of her baby surviving the first year. For those below average, this dropped to 75 percent. 



Among females without any close kin, the trend was stronger. A single unit rise in sociality increased survival odds by over 17 times.



<h2 class="wp-block-heading" id="h-kinship-and-male-alliances">Kinship and male alliances </h2>



The researchers ran extra tests to see if the benefit was just from living with relatives. It was not. They also checked if relationships with <a href="https://www.earth.com/news/from-rumbles-to-rituals-scientists-map-the-cultures-of-the-animal-kingdom/">males</a> helped. That also came up short.



“That tells us it’s not just about being born into a supportive family,” said Feldblum. “These are primarily social relationships with non kin.”



Even when female kin were present, they had no direct effect on offspring survival. Instead, they raised the chance that a mother had strong friendships. But it was those friendships, not the family ties, that made the difference.



<h2 class="wp-block-heading" id="h-social-ties-remain-stable-over-time">Social ties remain stable over time</h2>



The benefits of bonding were not a one time fluke. Females who were social before birth stayed social after birth too. Their social worlds remained steady. 



“Our results don’t prove causation, but they point to the value of being surrounded by others who support you, or at least tolerate you,” said Feldblum.



This was not the case for bonds with males. Social connections between male and female chimpanzees were less stable and showed no link to baby survival.



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



How do these friendships help? The exact mechanism remains uncertain. Social bonds might protect chimpanzee mothers from aggression. They could mean better access to food. Friendships might even prevent infanticide.



Earlier studies in this same group of chimps estimated that infanticide by other females may cause 3.5 percent to 19 percent of deaths in the first year. <a href="https://www.earth.com/news/social-curiosity-starts-young-and-helps-us-survive/">Social</a> mothers may face less of that risk.



More research is needed, but one thing is clear. Socially connected females stay in better shape, which could boost prenatal health. Unlike rank or dominance, which did not correlate with survival during this study window, sociality kept its value.



<h2 class="wp-block-heading" id="h-social-chimps-mirror-humans">Social chimps mirror humans</h2>



Though females often move away from family, they form lasting ties with unrelated females. The Gombe chimps mirror women in human patrilocal societies, who build networks after moving for marriage.



“We humans are remarkably collaborative and cooperative. We cooperate at scales that are pretty much unique in the animal kingdom,” said Feldblum. 



“Human females who don’t have access to kin, for example because they moved to a new city or village, are still able to form strong bonds that can benefit them.”



This study adds to the growing body of evidence that friendship matters. In baboons, dolphins, and horses, social bonds also improve reproductive success. In chimps too, strong bonds give babies a better chance at life.



Studying these dynamics in our closest relatives helps us understand our own nature. Like chimps, human survival does not just depend on strength or status. It depends on others. 



The study is published in the journal <a href="https://www.sciencedirect.com/science/article/pii/S2589004225011241" target="_blank" rel="noreferrer noopener">iScience</a>.



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Babies of social chimpanzee mothers are more likely to survive

In the wild, social lives shape survival. For female chimpanzees,...

Gorillas, often thought of as ground dwellers, spend much more time in the trees than previously assumed. This finding from the Max Planck Institute challenges long-standing ideas about the anatomy and evolution of gorillas.



Western and Bwindi mountain <a href="https://www.earth.com/news/gorillas-are-digging-for-a-surprising-food-in-the-jungle-soil/">gorillas</a>, studied across Gabon and Uganda, were observed over many years. Even the largest males, weighing up to 170 kg, showed substantial tree use. 



Adult females in Loango spent 34% of their time in trees, while Bwindi females clocked 21%. That is a huge jump from the 7% figure for Virunga gorillas.



Study lead author Dr. Martha M. Robbins is a zoologist in the Department of Primate Behavior and Evolution at the <a href="https://www.eva.mpg.de/index/">Max Planck Institute</a> for Evolutionary Anthropology.



“Adult females spent 20% to 30% of their time in the trees, while silverbacks spent 18% to 20% of their time being arboreal, which is much more than 2 to 7% found previously in the Virunga mountain gorillas,” said Dr. Robbins.



<h2 class="wp-block-heading" id="h-different-gorillas-different-tree-habits">Different gorillas, different tree habits</h2>



The Virunga population shaped our early understanding of <a href="https://www.earth.com/news/some-gorillas-get-sick-from-being-too-social/">gorilla</a> habits. These highland gorillas live in fruit-scarce zones and rarely climb. But the new study included data from five groups in Bwindi and one in Loango, totaling nearly 5,200 observation days.



The findings are clear: tree use varies widely between populations. Even juveniles and subadults in Bwindi and Loango spent 32% to 43% of their time in trees - double the rate seen in Virunga’s younger gorillas.



The researchers also found that body size plays a role but does not prevent tree climbing. 



“This demonstrates that the large body size of gorillas is not necessarily a limiting factor to tree climbing and that gorillas can be just as arboreal as some chimpanzee populations,” said co-author Rhianna Drummond-Clarke.



<h2 class="wp-block-heading" id="h-climbing-is-not-just-about-fruit">Climbing is not just about fruit</h2>



The researchers expected fruit to be the main driver behind climbing. While gorillas did climb more while eating fruit, the full story is more complex. In Loango, adult females were more arboreal when eating leaves than fruit. In Bwindi, the reverse was true.



Even silverbacks, the heaviest individuals, climbed trees to eat fruit. At Bwindi, silverbacks were arboreal 82% of the time they ate fruit. But fruit formed just 14% of their diet, meaning most of their tree time involved eating leaves.



At Loango, gorillas often ate fallen fruit from the ground. This shows fruit-eating can be a terrestrial act too. Meanwhile, western gorillas also ate lots of tree leaves, about 30% of their diet, driving folivorous tree use, similar to some monkeys.



<h2 class="wp-block-heading" id="h-feeding-is-the-main-reason-to-climb">Feeding is the main reason to climb</h2>



What were the <a href="https://www.earth.com/news/male-infertility-humans-linked-same-genes-gorilla-small-penises/">gorillas</a> doing in trees? Mostly feeding. Adult female gorillas were far more likely to climb while feeding than when resting or traveling.



Even when eating nonfruit, Loango females climbed more than Bwindi ones. This likely reflects differences in diet and foraging strategy. The energy payoff from fruit seems to outweigh the climbing cost, especially for massive silverbacks.



Also, Loango females were heavier climbers than their Bwindi peers when not eating fruit. This surprising reversal shows that even leaf-seeking gorillas may spend considerable time off the ground.



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



These results have big implications. <a href="https://www.earth.com/news/most-endangered-primate-species-identified-in-new-report/">Gorillas</a> have long been labeled as terrestrial because of their bulk and plant-heavy diets. But that view no longer holds. The study shows gorilla arboreality spans all life stages, from infants to adults.



That shift affects how we interpret the fossil record. Gorilla-like bones have been taken to suggest ground-based life. But frequent tree climbing changes the picture. 



“We demonstrate that large body size and a largely folivorous diet in apes are also consistent with frequent arboreality,” noted the study authors.



Studies of limb proportions and bone strength now suggest a range, from more tree-based western gorillas to more ground-based Virunga ones. 



This means our models of ancient human relatives may need adjustment. Gorilla-like features may not imply they lived solely on the ground.



<h2 class="wp-block-heading" id="h-gorillas-are-tree-climbers-not-just-walkers">Gorillas are tree climbers, not just walkers</h2>



Gorillas are not just forest-floor giants. They climb often and for various reasons. From feeding on leaves to exploring the canopy, these behaviors offer key insights into how apes, including humans, evolved.



Future research may look into how such large animals navigate trees. They might distribute their weight across branches or use special movement strategies, similar to orangutans or chimpanzees. 



This research opens new doors in our understanding of ape mobility and evolutionary history.



The study is published in the journal <a href="https://www.cell.com/current-biology/fulltext/S0960-9822(25)00590-1" target="_blank" rel="noreferrer noopener">Current Biology</a>.



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Gorillas spend much more time in trees than we previously thought

Gorillas, often thought of as ground dwellers, spend much more...

When humans burst into laughter together, moods lift almost automatically. New research shows that a similar boost happens in our closest cousins.



An international team led by <a href="https://bloomington.iu.edu/">Indiana University</a> scientists has discovered that <a href="https://www.earth.com/news/bonobos-group-cohesion-common-enemy-effect-do-not-kill-inside-their-species/">bonobos</a> become more upbeat after hearing the giggles of their companions. This finding pushes the evolutionary history of positive emotions back millions of years.



<h2 class="wp-block-heading" id="h-laughter-changed-ape-choices">Laughter changed ape choices</h2>



To explore laughter’s influence, the researchers designed a cognitive-bias test often used in animal psychology to gauge optimism or pessimism.



First, they trained bonobos at the <a href="https://www.apeinitiative.org/">Ape Initiative</a> in Des Moines, Iowa, to recognize two kinds of boxes: black ones that always contained a delicious snack and white ones that were always empty.



Once the apes consistently chose black and ignored white, the experimenters introduced a third, ambiguous gray box. They then played one of two sounds: recorded bonobo laughter or a neutral control noise.



“We know that other apes, like chimpanzees, have contagious laughter during play," said lead author Sasha Winkler, a primatologist at <a href="https://duke.edu/">Duke University</a>. "We were wondering if that behavior could be explained by positive emotions produced from the sound itself.” 



If the bonobos felt a surge of good feeling after hearing laughter, the team expected them to treat the uncertain gray box as if it were the rewarding black one.



That is exactly what happened. “Think of it like the rose-colored glasses effect,” Winkler said. “The bonobos were much more likely to approach the gray boxes after hearing laughter, treating them like the rewarded boxes, and indicating a more optimistic expectation of finding a treat.”



<h2 class="wp-block-heading" id="h-tracing-optimism-to-our-ancestors">Tracing optimism to our ancestors</h2>



This study is the first experimental proof that great-ape laughter can shift mood and cognition the way human laughter does.



“The tendency to behave more optimistically after hearing laughter suggests that the sound alone induced a positive emotional state in bonobos,” said senior author Erica Cartmill, the director of Indiana University’s Cognitive Science Program.



“This is the first study of which we're aware to measure a positive affect shift in nonhuman primates from a brief experimental intervention.”



Great apes -&nbsp; bonobos, <a href="https://www.earth.com/news/what-wild-chimpanzees-can-teach-us-about-parenting/">chimpanzees</a>, gorillas, orangutans - all emit play calls that acoustically resemble human chuckles. Earlier work tied those sounds to a common evolutionary origin. The new findings add a cognitive twist.



“Our results suggest that laughter in other apes shares not only phylogenetic and behavioral similarities with human laughter but also perhaps some of the same cognitive-emotional underpinnings,” Winkler noted.



“This emotional contagion appears to have been present in the primate lineage long before the evolution of language.”



<h2 class="wp-block-heading" id="h-laughter-empathy-and-apes">Laughter, empathy, and apes</h2>



Emotional contagion is often described as a foundational element of <a href="https://www.earth.com/news/little-benjamina-the-oldest-evidence-of-social-empathy-in-humans/">empathy</a> - the capacity to share another’s feelings. As Winkler put it, “studies like ours can help to untangle the evolutionary building blocks of empathy, communication, and cooperation in humans.”



By revealing that a simple vocal cue can brighten outlooks in bonobos, the research suggests that the mechanisms linking social sound to positive mood were already in place in a common ancestor millions of years ago.



Cartmill added that the work answers a long-standing bias in emotion research. “Our emotions influence many aspects of cognition, including memory, attention, and decision-making, but research has historically focused on negative emotions with clear behavioral correlates, like <a href="https://www.earth.com/news/brain-pathway-discovered-that-suppresses-fear/">fear</a> and aggression.”



“We wanted to better understand the relationship between positive affect and cognition in our closest living relatives.”



<h2 class="wp-block-heading" id="h-kanzi-and-the-future-of-empathy">Kanzi and the future of empathy</h2>



The experiments involved four bonobos, including the celebrated language-using ape Kanzi, who recently passed away.



“I feel incredibly grateful to have had the opportunity to work with Kanzi while he was still alive,” Winkler said. 



“We hope this brings greater public awareness of the remarkable similarities between us and bonobos, who are an endangered species. We have so much to learn from these incredible animals.”



Future studies will test whether laughter exerts similar cognitive effects in chimpanzees and other primates. They will also explore how social context - for example, hearing laughs from friends versus strangers - modulates optimism.



For now, the discovery that bonobo giggles brighten expectations highlights a shared emotional heritage and hints that a simple laugh has been boosting group spirits since long before humans walked the Earth.



The study is published in the journal <a href="https://www.nature.com/articles/s41598-025-02594-8">Nature Scientific Reports</a>.



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Laughter lifts bonobo moods, offering clues to human emotion

When humans burst into laughter together, moods lift almost automatically....

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