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

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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Chimpanzees copy strange, useless trends just like humans do

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

Walk into any drugstore or open TikTok - everywhere you look, skin care products are calling your name. They promise miracles - clear <a href="https://www.earth.com/news/our-skins-bacteria-could-be-a-natural-sunscreen/">skin</a>, no wrinkles, no acne. But how do you know what works, especially now, with summer heating up?



Here’s the problem. The more products there are, the harder it gets to make sense of it all. You try one cream, then another, but still don't know what to choose. Luckily, a new study cuts through the noise.



<h2 class="wp-block-heading" id="h-ingredients-for-common-skin-problems">Ingredients for common skin problems</h2>



A research team at Northwestern University <a href="https://www.feinberg.northwestern.edu/index.html" target="_blank" rel="noreferrer noopener">Feinberg School of Medicine</a> set out to clarify skin care confusion. 



They identified ingredients that dermatologists most often recommend for seven common skin concerns. The study helps bridge the gap between marketing claims and actual results.



The project was led by Dr. Murad Alam, an expert in dermatology at Northwestern. His research provides a much-needed foundation for consumers seeking trustworthy information. 



According to the study, one of the most highly recommended ingredients is <a href="https://health.clevelandclinic.org/mineral-vs-chemical-sunscreen" target="_blank" rel="noreferrer noopener">mineral sunscreen</a>. It shields skin from wrinkles, redness, and dryness. 



<a href="https://www.henryford.com/blog/2022/10/what-you-need-to-know-about-retinoids" target="_blank" rel="noreferrer noopener">Retinoids</a>, derived from vitamin A, also earned strong endorsements. Dermatologists trust them to reduce acne, wrinkles, dark spots, large pores, and oily skin.



The full study lists ingredients matched to specific <a href="https://www.earth.com/news/future-tech-will-track-emotions-through-changes-in-our-skin/">skin</a> problems. These findings allow consumers to focus on what works best for their unique needs.



<h2 class="wp-block-heading" id="h-selecting-the-most-effective-ingredients">Selecting the most effective ingredients</h2>



This study isn’t based on guesses. It followed a method called <a href="https://www.investopedia.com/terms/d/delphi-method.asp">Delphi consensus</a> - a fancy name for a simple process. Experts rate ingredients, talk about them, and then rate them again.



Dozens of dermatologists took part. They gave each ingredient a score from 1 to 9. Then they discussed the results. After a second round of scoring, only the top-rated ingredients stayed on the list.



“This is the first time experts have come together nationally to cut through the overwhelming number of skin care options,” said Dr. Alam. 



“We wanted to help both doctors and everyday users understand which ingredients are backed by the most expert support.”



<h2 class="wp-block-heading" id="h-fewer-skin-care-products-work-best">Fewer skin care products work best</h2>



Many people assume that using more <a href="https://www.earth.com/news/vitamin-c-promotes-skin-renewal-and-anti-aging-at-the-genetic-level-dna-demethylation/">products</a> leads to better results - a cleanser here, a serum there, and a moisturizer on top. It seems like more effort should mean better skin.



Dr. Alam strongly disagrees. “Using too many products can irritate your <a href="https://www.earth.com/news/teen-skin-bacteria-could-hold-the-secret-to-acne-prevention/">skin</a> and make things <a href="https://www.earth.com/news/common-plastics-chemical-bpa-linked-to-autism-adhd-in-children/">worse</a>,” he said. “It’s about knowing which ingredients are most effective for your specific concerns and are best for your routine.”



This matters, especially now, with social media hyping endless skin routines. Simplicity works best. Too many layers may backfire. Your skin doesn’t need a ten-step routine. It needs smart choices.



<h2 class="wp-block-heading" id="h-skin-care-products-are-not-strictly-tested">Skin care products are not strictly tested</h2>



There's another reason this study is noteworthy: skincare products aren’t held to the same rigorous standards as medications. 



While drugs must pass strict testing by the U.S. Food and Drug Administration, your favorite serum typically bypasses that level of scrutiny.



Dr. Alam noted that most cosmetic products lack scientific review. This study fills that gap. The purpose is simple - give people a clearer path to healthier skin.



<h2 class="wp-block-heading" id="h-simplify-your-skin-care-routine-nbsp">Simplify your skin care routine&nbsp;</h2>



Summer has fully arrived, bringing longer, hotter days along with plenty of sun exposure. This season often leads to more sweating, increased oiliness, and various skin problems such as breakouts, redness, and dryness. 



It is a time when your skin needs extra care and protection, but that does not mean you need a complicated routine. This is the perfect moment to simplify how you take care of your skin. 



Dermatologists recommend focusing only on ingredients that are backed by strong research and expert agreement, such as mineral sunscreen and retinoids. These ingredients have been shown to work effectively for many skin concerns.



<h2 class="wp-block-heading" id="h-stick-with-what-works">Stick with what works</h2>



It is easy to get distracted by every new product that appears in stores or on social media. However, constantly switching between trendy products can do more harm than good. 



Instead, stick with what works. Choose the ingredients that dermatologists trust. Be consistent with your routine and, over time, your skin will show improvements.



New products will continue to appear in beauty stores. Brands will keep releasing items that promise fast results. But now, you can make smarter choices by focusing on proven solutions instead of getting caught up in every trend.



The study is published in the <a href="https://www.jaad.org/article/S0190-9622(25)00612-7/abstract" target="_blank" rel="noreferrer noopener">Journal of the American Academy of Dermatology</a>.



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These are the very best skin care ingredients, according to an in-depth national study

Walk into any drugstore or open TikTok - everywhere you...

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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

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

Wheat is a major part of our diet, especially in the form of bread. But not all wheat is the same - and the way in which it’s grown, processed, and baked affects the nutrients that are present in it.



Until now, the wheat industry has mostly focused on boosting yields, reducing inputs like fertilizers and pesticides, and ensuring good baking quality. 



What often gets overlooked, however, is that wheat can also be a valuable source of nutrients. In fact, it contributes over 20% to the global supply of fiber, minerals, and trace elements, according to the Food and Agriculture Organization (<a href="https://www.fao.org/home/en" target="_blank" rel="noreferrer noopener">FAO</a>).



But getting more nutrition out of wheat isn’t just about planting a different variety. It involves the entire chain - all the way from the field to the oven.



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



Bread can be surprisingly diverse when it comes to nutrition. A slice of <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC5310957/" target="_blank" rel="noreferrer noopener">whole grain bread</a>, for instance, can pack a good amount of fiber, <a href="https://www.earth.com/news/vitamin-b-paradox-supplement-linked-to-heart-disease-risk/">B vitamins</a>, iron, magnesium, and complex carbs. These nutrients help regulate blood sugar, support digestion, and provide long-lasting energy. 



On the flip side, white bread - made from refined flour - loses much of that fiber and many <a href="https://www.earth.com/news/micronutrient-deficiency-rates-are-soaring-worldwide/">micronutrients</a> during processing. Manufacturers often enrich it to add some of those nutrients back, but it still doesn’t match the nutritional punch of whole grain varieties.



The kind of bread you eat matters, but so does how much. Bread is a carb-heavy food, and while carbs aren't the enemy, overdoing them - especially if the bread is low in fiber - can spike your blood sugar and leave you hungrier sooner. 



If you're aiming for a more nutritious option, look for loaves with at least 3 grams of fiber and minimal added sugar. Bonus points for sprouted grains, seeds, or sourdough, which can improve digestion and nutrient absorption.



<h2 class="wp-block-heading" id="h-characteristics-of-wheat-varieties">Characteristics of wheat varieties </h2>



Scientists at the <a href="https://www.uni-hohenheim.de/en" target="_blank" rel="noreferrer noopener">University of Hohenheim</a> and the University Medical Center at the <a href="https://www.uni-mainz.de/en/" target="_blank" rel="noreferrer noopener">University of Mainz</a> teamed up with four wheat breeding companies to study how wheat’s nutritional value can be improved across the whole value chain.



Over five years, they recorded more than 6,000 traits across 282 wheat varieties and 400 breeding lines.



Dr. Friedrich Longin is director of the Wheat Department at the <a href="https://lsa.uni-hohenheim.de/" target="_blank" rel="noreferrer noopener">State Plant Breeding Institute</a> and coordinator of the <a href="https://lsa.uni-hohenheim.de/en/betterwheat_en" target="_blank" rel="noreferrer noopener">Betterwheat project</a>.



“The unique thing about the project was the holistic view of variety characteristics along the entire value chain,” explained Dr. Longin.



“In addition to important characteristics for successful cultivation, several dozen processing characteristics for bakeries were considered, as well as important ingredients and proteins that could be important for <a href="https://www.earth.com/news/proper-nutrition-in-the-first-1000-days-of-life-is-crucial/">human</a> nutrition.”



<h2 class="wp-block-heading" id="h-some-wheat-just-has-more-nutrients">Some wheat just has more nutrients</h2>



The wheat varieties were tested in different environments across Europe to measure how both breeding and growing conditions influence the traits of the wheat.



“This allows us to estimate the extent of the influence of breeding, but also that of the growing environment, on these many traits,” noted Dr. Johannes Schacht, senior wheat breeder at <a href="https://www.limagrain.com/en">Limagrain</a> GmbH.



One of the team's main goals was to understand how nutrient levels vary between wheat types. They tested about 800 wheat samples for 13 key minerals and trace elements like iron and <a href="https://www.earth.com/news/calcium-zinc-are-keys-to-healthier-pregnancy/">zinc</a> - nutrients that are important for immunity, metabolism, and cell health.



“We were able to determine that the nutrient content in different wheat varieties varies greatly - and can fluctuate by up to 50%,” stated Dr. Longin.



“Our trials also show that the nutrients in wheat can be combined well with the required baking qualities in terms of breeding. These correlated positively with the protein content and dough properties.”



<h2 class="wp-block-heading" id="h-measuring-wheat-nutrient-content">Measuring wheat nutrient content</h2>



To apply this research practically, the scientists explored how to quickly measure nutrient content in wheat. 



One method, x-ray fluorescence (XRF) spectrometry, could be a game changer. It scans wheat with X-rays and, based on prior calibrations, provides fast, reliable nutrient readings.



“In order to use this knowledge in practice, xrf fluorescence spectrometry is a method that can be used to measure the nutrient content in wheat quickly and reliably,” explained Dr. Longin.



But using this technology widely would require investment. “This is only possible if the additional work is also paid for,” he added.



And there’s another catch: boosting wheat’s nutrition only makes a difference if people eat more <a href="https://www.earth.com/news/refined-grains-increase-the-risk-of-heart-disease/">whole grains</a> or at least <a href="https://www.earth.com/news/chocolate-with-less-sugar-still-tastes-great-with-a-secret-ingredient/">flours</a> with high type numbers (1050 and up). 



That’s because most nutrients are in the outer layers of the grain, which are lost in refined flours like types 405, 550, and 812.



<h2 class="wp-block-heading" id="h-bakers-make-wheat-digestible">Bakers make wheat digestible</h2>



Even if wheat is nutrient-rich, our bodies might not absorb those nutrients unless the bread is <a href="https://www.earth.com/news/freezing-bread-could-make-it-healthier/">baked</a> the right way.



“The healthy ingredients in wheat are bound in phytic acid. However, this acid cannot be digested and is excreted along with the beneficial nutrients,” said Dr. Longin.



So the researchers partnered with artisan bakers to test four common baking methods. One technique stood out: combining a long dough cycle with sourdough. 



“We found that the phytic acid is almost completely broken down during this baking process, making the ingredients available to the body,” he said.



<h2 class="wp-block-heading" id="h-better-bread-starts-with-better-choices">Better bread starts with better choices</h2>



From field to bakery, everyone involved in wheat production can help improve the nutritional value of bread. But it starts with us.



“All partners in the wheat value chain can influence the nutritional content of bread,” said Dr. Longin. "However, clear priorities must be set: first of all, we consumers should eat more whole grains." 



"This should then be baked with a long leavening process, and only then does breeding and targeted grain trading make sense in order to further optimize the nutrient profile."



Wheat offers more than just <a href="https://www.earth.com/news/eating-almonds-can-help-you-cut-calories/">calories</a>. With the right science, baking methods, and consumer choices, it can play a much bigger role in a healthy diet.



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Study reveals how to make wheat bread even healthier while also improving taste

Wheat is a major part of our diet, especially in...

Copper wires snake through every electric motor, power line, and rooftop solar panel on the planet. Demand for the metal is rising so fast that the International Energy Agency projects a 50 percent jump by 2040 in its net‑zero scenario.



A new study shows that some of Earth’s richest copper troves owe their existence not to ongoing subduction zones, but to the long‑lasting <a href="https://www.earth.com/news/discovery-of-a-20-million-ton-copper-super-deposit/">chemical</a> aftershocks of a continental collision in southern Tibet.



The analysis includes contributions from Dr. Yongjun Lu of the School of Earth and Oceans at the <a href="https://www.uwa.edu.au/home">University of Western Australia</a>.



<h2 class="wp-block-heading" id="h-copper-demand-is-soaring">Copper demand is soaring</h2>



Copper’s unmatched ability to move electrons makes it the backbone of electric vehicles, heat pumps, and sprawling renewable‑energy grids. Two tons of copper may hide inside a utility‑scale wind turbine, while an electric car uses roughly three times more than a gasoline model.



More than half of the global resource sits in <a href="https://www.nature.com/articles/s43247-022-00440-7" target="_blank" rel="noreferrer noopener">porphyry copper deposit</a> clusters, gigantic ore bodies formed by mineral‑rich fluids rising from cooling magma. They are the workhorses of modern mining because a single district can run for decades.



Yet many prospective belts lie high in the Andes, Himalayas, or other remote ranges where exploration is costly and climate risks loom. 



Predicting which mountains hide <a href="https://www.earth.com/news/amount-of-copper-needed-to-power-tech-and-develop-the-world-is-astonishing-not-enough/">ore</a> and which hide barren rock has become an urgent economic puzzle.



Exploration teams scour trace‑element maps, but ore‑forming magmas can emerge tens of millions of years after an oceanic plate vanished. The Tibetan discovery uncovers why that delay happens, and how to spot it.



<h2 class="wp-block-heading" id="h-ancient-collision-sparked-copper-deposits">Ancient collision sparked copper deposits</h2>



The <a href="https://www.science.org/doi/10.1126/sciadv.adx4474" target="_blank" rel="noreferrer noopener">Gangdese Belt</a> in southern Tibet holds more than 45 million tons of copper spread across <a href="https://www.sciencedirect.com/topics/earth-and-planetary-sciences/miocene" target="_blank" rel="noreferrer noopener">Miocene‑age</a> porphyries. 



Those deposits erupted between 18 and 13 million years ago, long after the Neo‑Tethys seafloor slid beneath Asia and broke off.



Researchers sampled igneous <a href="https://www.earth.com/news/geologists-discover-the-largest-copper-gold-and-silver-deposit-in-the-last-three-decades/">rocks</a> spanning the entire subduction‑collision cycle. They grouped them into precollisional, syncollisional, and postcollisional suites, then tracked how each generation changed.



Both <a href="https://www.scandium.org/scandium-and-vanadium-similarities-and-differences/" target="_blank" rel="noreferrer noopener">vanadium‑to‑scandium ratios</a> and <a href="https://www.sciencedirect.com/science/article/abs/pii/S0016703724000486" target="_blank" rel="noreferrer noopener">zircon oxygen‑fugacity</a> indicators spiked in the post‑collision magmas. 



That jump signaled a surge of oxidized material, exactly what copper needs to stay dissolved until the magma reaches the shallow crust.



“This finding challenges the notion that only oceanic subduction introduces such oxidants into the mantle,” explained Dr. Lu.



<h2 class="wp-block-heading" id="h-tracking-copper-s-rocky-origin">Tracking copper’s rocky origin</h2>



To figure out where the extra oxygen came from, the researchers looked at <a href="https://www.earth.com/news/one-of-the-worlds-largest-copper-gold-and-silver-deposits-discovered-at-very-high-altitude/">chemical</a> fingerprints left behind in the rocks. 



They studied <a href="https://www.sciencedirect.com/topics/earth-and-planetary-sciences/mercury-isotopes" target="_blank" rel="noreferrer noopener">mercury isotopes</a>, which hold onto their unique signature even after going through intense heat and pressure. In the post-collision rocks, that signature pointed to surface sediments, not deep mantle sources.



The team also examined magnesium isotopes in volcanic rocks called ultrapotassic lavas and found unusually light values. This kind of reading is a known sign of recycled carbonate material. 



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/copper-deposit-formation_magmatic-redox_illustration_credit-Science-Advances_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/copper-deposit-formation_magmatic-redox_illustration_credit-Science-Advances_1s.webp" alt="How copper deposits form. Evolution of magmatic redox from oceanic subduction to continental collision. Credit: Science Advances (2025)" class="wp-image-1977073"/></a><figcaption class="wp-element-caption">How copper deposits form. Evolution of magmatic redox from oceanic subduction to continental collision. Click image to enlarge. Credit: Science Advances (2025)</figcaption></figure>



Together, the results showed that sediments from the Indian plate had sunk deep underground and played a major role in creating the copper-rich magma.



Mercury‑isotope work on porphyry systems elsewhere has reached similar <a href="https://www.science.org/doi/10.1126/sciadv.adp7383" target="_blank" rel="noreferrer noopener">conclusions</a>, reinforcing the method as a global tracer of recycled surface material.



<h2 class="wp-block-heading" id="h-crustal-material-fuels-deposits">Crustal material fuels deposits</h2>



Carbonate layers from the Indian margin, rich in calcium and trapped CO2, rode the downgoing slab. At depths near 60 miles and temperatures above 1,600°F, those carbonates reacted with iron‑bearing mantle minerals. 



The redox exchange turned ferrous iron into ferric iron, pushing the <a href="https://chem.libretexts.org/Bookshelves/Analytical_Chemistry/Supplemental_Modules_(Analytical_Chemistry)/Electrochemistry/Redox_Chemistry/Oxidation_States_(Oxidation_Numbers)" target="_blank" rel="noreferrer noopener">oxidation state</a> of the mantle wedge higher.



<a href="https://agupubs.onlinelibrary.wiley.com/doi/abs/10.1002/9781119473206.ch5" target="_blank" rel="noreferrer noopener">Oxidized mantle melts</a> can carry sulfur as sulfate instead of sulfide. That subtle chemical switch lets copper remain in solution rather than being locked away in early sulfide droplets. When the melt stalls in the mid‑crust, pressure drops and fluids separate, precipitating copper sulfides that build an ore shell.



“Think of it as a second wind for copper‑forming magmas, even after the oceanic plate is gone, recycled crustal sediments can continue to fuel metal‑rich systems for millions of years,” said Lu.



<h2 class="wp-block-heading" id="h-finding-copper-from-ancient-collisions">Finding copper from ancient collisions</h2>



Most exploration models steer geologists toward active volcanic arcs. The new Tibetan evidence widens the hunting ground to include fossil arcs sitting above former collision zones. 



Provinces such as the Zagros in Iran or the <a href="https://www.britannica.com/place/Lesser-Caucasus" target="_blank" rel="noreferrer noopener">Lesser Caucasus</a> share similar histories of carbonate‑rich continental subduction.



“It changes the way we think about where and how to look for giant copper deposits and highlights the potential of post‑subduction settings, particularly those involving continent‑continent collision, as important frontiers for exploration,” noted Lu.



Mercury and magnesium isotope surveys no longer belong only in academic labs. They can flag hidden oxidized corridors before expensive drilling begins, saving both time and shareholder cash.



<h2 class="wp-block-heading" id="h-what-it-means-for-clean-energy">What it means for clean energy</h2>



Copper supply already trails projected demand. Without fresh discoveries, shortages could slow grid upgrades or inflate the cost of electric cars. 



By demonstrating that continent‑continent collisions can keep ore‑forming magmas alive long after subduction halts, the Tibetan study offers practical hope.



Companies willing to brave high‑altitude logistics may unlock deposits that standard models overlook. Nations rich in orogenic belts gain leverage in critical‑minerals diplomacy, while resource-poor regions must double down on recycling and substitution.



The study shows that plate tectonics still shapes the economics of decarbonization, one oxidized magma batch at a time.



The study is published in the journal <a href="https://www.science.org/doi/10.1126/sciadv.adp7383" target="_blank" rel="noreferrer noopener">Science Advances</a>.



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Scientists finally discover how giant copper deposits form around the world

Copper wires snake through every electric motor, power line, and...

Astronomers have recently added a new member to the small club of confirmed interstellar objects. The icy wanderer, known as 3I/Atlas, was officially recognized this week by the International Astronomical Union’s Minor Planet Center (MPC).



Observations showed it is racing through the solar system on a hyperbolic path - one that will carry it back into interstellar space after a brief celestial cameo.



<h2 class="wp-block-heading" id="h-a-fuzzy-comet-with-incredible-speed">A fuzzy comet with incredible speed</h2>



Early images of 3I/Atlas revealed the hazy glow typical of a <a href="https://www.earth.com/news/most-anticipated-comet-of-2024-returns-this-weekend-after-80000-years/">comet</a>. “It looks kind of fuzzy,” said Peter Veres, an astronomer at the <a href="https://www.minorplanetcenter.net/">MPC</a> who helped confirm the object’s status. “It seems that there is some gas around it, and I think one or two telescopes reported a very short tail.”



That fuzzy halo is created as sunlight warms the comet’s surface, releasing dust and gas that trail behind it. Current estimates suggest the nucleus spans six to 12 miles (10 to 20 kilometers). 



Because icy bodies reflect sunlight efficiently, the true size may prove smaller if the surface is especially bright.



What is certain is the object’s speed. Preliminary calculations put its velocity at more than 60 km per second (roughly 135,000 mph). At that speed, solar <a href="https://www.earth.com/news/gravity-could-be-the-definitive-clue-that-the-universe-is-a-computer-storing-information/">gravity</a> cannot capture it, confirming its extrasolar origin.



<h2 class="wp-block-heading" id="h-spotting-an-interstellar-traveler">Spotting an interstellar traveler</h2>



The discovery began on Tuesday when a telescope in Chile, operated as part of the NASA-funded <a href="https://atlas.fallingstar.com/">ATLAS survey</a>, recorded an unfamiliar, rapidly moving speck. 



Within hours, professional and amateur observers worldwide had combed archival data, tracing its motion back to at least June 14. 



The collected positions fit a hyperbolic orbit - unmistakable evidence the object is diving in from beyond the Sun’s gravitational reach.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/31-atlas_interstellar-comet_diagram_NASA_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/31-atlas_interstellar-comet_diagram_NASA_1s.webp" alt="This diagram shows the trajectory of interstellar comet 3I/ATLAS as it passes through the solar system. It will make its closest approach to the Sun in October. Credit: NASA/JPL-Caltech" class="wp-image-1977069"/></a><figcaption class="wp-element-caption">This diagram shows the trajectory of interstellar comet 3I/ATLAS as it passes through the solar system. It will make its closest approach to the Sun in October. Click image to enlarge. Credit: NASA/JPL-Caltech</figcaption></figure>



Richard Moissl, head of planetary defense at the <a href="https://www.esa.int/">European Space Agency</a>, emphasized that 3I/Atlas poses no danger. 



“It will fly deep through the <a href="https://www.earth.com/news/astronomers-announce-evidence-suggesting-that-our-solar-system-has-nine-planets-again/">solar system</a>, passing just inside the orbit of Mars,” he said, adding that the flyby comes nowhere near a collision with Earth or the Red Planet.



Calculations show the interstellar comet will reach perihelion, its closest point to the Sun, on 29 October, then fade as it speeds back into the darkness over the next few years.



<h2 class="wp-block-heading" id="h-how-interstellar-comets-differ">How interstellar comets differ</h2>



Unlike comets bound to the Sun, interstellar objects are born around distant stars. Jonathan McDowell of the <a href="https://www.cfa.harvard.edu/">Harvard–Smithsonian Center for Astrophysics</a> explained the likely origin scenario.



“We think that probably these little ice balls get formed associated with star systems. And then as another star passes by, tugs on the ice ball, frees it out. It goes rogue, wanders through the galaxy, and now this one is just passing us,” he said.



In 2017, astronomers found the first known example, 1I/ʻOumuamua, whose odd shape and tumbling motion sparked contentious debate - including speculation it might be alien technology.



Two years later came 2I/Borisov, a more conventional comet with clear gas jets. 3I/Atlas now becomes the largest and fastest of the trio, offering scientists a fresh specimen to study.



<h2 class="wp-block-heading" id="h-observations-of-a-fast-moving-comet">Observations of a fast-moving comet</h2>



The MPC initially labeled the body A11pl3Z, but the “3I” prefix signifies its confirmed interstellar status. As data pours in, researchers aim to refine its orbit, rotation rate, and composition. 



Scientists are particularly eager to learn whether its chemistry differs from solar system comets, which would provide clues about its natal environment.



Despite enthusiasm, a spacecraft intercept is beyond reach, since there is not enough time to plan, launch, and meet with an object moving this quickly and appearing on such short notice. 



Ground-based and space-based telescopes will therefore carry the observational load, capturing spectra and high-resolution imagery while the interstellar comet remains within range.



<h2 class="wp-block-heading" id="h-interstellar-objects-may-be-common">Interstellar objects may be common</h2>



Mark Norris, an astronomer at the University of Central Lancashire, pointed out an intriguing statistic: modeling work suggests up to 10,000 interstellar objects could be drifting inside the solar system at any given moment - most of them too small or faint to detect.



The newly built <a href="https://www.earth.com/news/first-images-from-the-vera-c-rubin-observatory-are-breathtaking/">Vera C. Rubin Observatory</a> in Chile, scheduled to begin its wide-field survey soon, is expected to uncover many more. Such a flood of discoveries would transform the study of planetary system formation. 



Each passerby carries a chemical and physical record of processes that occurred around alien suns. They deliver natural “samples” at no cost other than the telescopic time required to study them.



<h2 class="wp-block-heading" id="h-fly-by-science-in-action">Fly-by science in action</h2>



Scientists will watch 3I/Atlas brighten through the northern autumn, hoping for unobstructed views of its coma chemistry.



Spectrographs on large telescopes may reveal ratios of carbon monoxide, carbon dioxide, and water vapor - benchmarks that help distinguish comets formed under different conditions. 



<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/-vzafaw0t08
</div></figure>



Photometric monitoring can nail down its spin. Careful astrometry will improve the orbit and may even hint at non-gravitational forces from asymmetric outgassing.



<h2 class="wp-block-heading" id="h-improving-planetary-defense-capabilities">Improving planetary defense capabilities </h2>



Beyond pure science, each interstellar detection enhances planetary defense capabilities. 



Rapidly identifying an object’s orbit and assessing any hazard is a rehearsal for future surprises - though, happily, none of the known interstellar visitors have posed a threat.



For now, astronomers relish the serendipity. A cosmic snowball born around an unknown star has swung through humanity’s celestial neighborhood, offering a fleeting chance to study matter forged in a far-off corner of the galaxy. 



With upgraded surveys on the horizon, the odds of such encounters - and the insights they carry - are only set to increase.



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Interstellar object appears out of nowhere and stuns astronomers with its size and speed

Astronomers have recently added a new member to the small...

A 3,000‑ton stack of metal and superconducting cable is taking shape in southern France. Engineers say it will cage star‑hot plasma and tip the scales toward commercial fusion power.



The massive structure, formally called the pulsed superconducting magnet system, sits at the center of <a href="https://www.iter.org/machine/what-tokamak" target="_blank" rel="noreferrer noopener">ITER’s tokamak reactor</a>. 



<a href="https://www.linkedin.com/in/karim-el-hamdani-7b5648151/?originalSubdomain=fr" target="_blank" rel="noreferrer noopener">Karim El Hamdani</a> from the ITER Organization leads the team racing to finish the cold‑test facility before assembly deadlines tighten.



<h2 class="wp-block-heading" id="h-size-matters-for-iter-fusion-energy">Size matters for ITER fusion energy</h2>



Fusion demands magnetic muscle. The <a href="https://www.ga.com/superconducting-magnets/iter-cs-fabrication" target="_blank" rel="noreferrer noopener">central solenoid</a> alone will stand 59 feet tall and weigh 1,000 tons, generating a 13‑tesla field strong enough to hoist an aircraft carrier. 



Add six ring‑shaped poloidal magnets and eighteen D‑shaped toroidal coils and the total reaches roughly 3,000 tons, holding plasma currents of 15 million amps.



ITER aims for a ten‑to‑one energy payoff, producing 500 megawatts of <a href="https://www.earth.com/news/nuclear-fusion-milestone-brings-clean-energy-closer-to-reality/">fusion</a> heat from 50 megawatts of external power. That target, known as Q ≥ 10, would mark a leap beyond every device built so far.



Each module of the central solenoid took over two years to build and test. The sixth and final module, weighing 110 tons, was fabricated and validated by <a href="https://www.ga.com/" target="_blank" rel="noreferrer noopener">General Atomics</a> in Poway, California.



Final tests included helium leak checks, insulation integrity, cooldowns to 4.5 Kelvin, and electrical charging to 48,500 amps. Once all modules are stacked in France, they’ll form a column nearly 60 feet tall at the heart of the tokamak.



<h2 class="wp-block-heading" id="h-what-makes-it-tick">What makes it tick</h2>



Each coil uses miles of niobium‑tin or niobium‑titanium wire cooled to 4 Kelvin, about −452 °F, where <a href="https://www.energy.gov/science/doe-explainssuperconductivity" target="_blank" rel="noreferrer noopener">superconducting</a> electrons move with zero resistance. 



Inside its own <a href="https://andor.oxinst.com/learning/view/article/what-is-a-cryostat" target="_blank" rel="noreferrer noopener">cryostat</a>, the new test facility will chill full‑scale coils and push up to 68,000 amps through them before they ever reach the reactor hall.



“We’ve gone from nothing to a design that is essentially finalized. This pace was possible because everybody stayed agile at ITER,” said El Hamdani. 



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/superconducting-magnet_ITER-constructions-site_ITER_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/superconducting-magnet_ITER-constructions-site_ITER_1s.webp" alt="Installation of the first superconducting magnet, Poloidal Field Coil #6, in the tokamak pit at the ITER construction site. The Central Solenoid will be mounted in the center after the vacuum vessel has been assembled. Credit: ITER Organization" class="wp-image-1977060"/></a><figcaption class="wp-element-caption">Installation of the first superconducting magnet, Poloidal Field Coil #6, in the tokamak pit at the ITER construction site. The Central Solenoid will be mounted in the center after the vacuum vessel has been assembled. Click image to enlarge. Credit: ITER Organization</figcaption></figure>



All of ITER’s magnets must operate near absolute zero to achieve superconductivity. This means circulating liquid helium through 18 miles of cryolines to maintain a steady 4.5 Kelvin, or −452 °F.



India built the <a href="https://www.iter.org/mach/Cryostat" target="_blank" rel="noreferrer noopener">cryostat</a>, a 98‑foot‑wide stainless steel chamber that houses the entire reactor system. At 3,850 tons, it is the largest high‑vacuum pressure chamber ever constructed for a fusion device.



<h2 class="wp-block-heading" id="h-testing-power-before-plasma">Testing power before plasma</h2>



Engineers have already started validating ITER’s heating systems using a full-scale prototype called <a href="https://www.iter.org/node/20687/successful-round-tests-mitica" target="_blank" rel="noreferrer noopener">MITICA</a>. 



Located in Padua, Italy, MITICA recently hit 710 kilovolts across its simulated acceleration stages, exceeding the 700-kilovolt goal set for ITER’s first campaign.



Even without the final beam source installed, MITICA’s electrostatic mock-up allowed teams to identify issues and refine shielding components. 



These early insights will help avoid problems during high-voltage neutral beam injection inside the main tokamak.



The window is narrow. Installation crews re‑purposed an old winding shop, upgraded its crane to lift 800‑ton loads, and ordered a 330‑ton cryostat built in parallel. 



Factory tests show the <a href="https://www.earth.com/news/floating-solar-panels-could-power-every-home-in-the-u-s/">power</a> system is 95 percent complete, with quench‑detection software nearly finished.



Horizontal testing demands a custom in‑cryostat feeder to route helium and power. Delivery is expected within weeks. Commissioning of support lines and vacuum pumps begins this month, even before the cryostat arrives on site.



<h2 class="wp-block-heading" id="h-iter-fusion-energy-and-earth-s-future">ITER fusion energy and Earth's future</h2>



Validation at −452 °F will shake out sensor glitches, coolant flow limits, and alignment tolerances measured in thousandths of an inch. Every problem solved in the test bay reduces risk when the same hardware slides into the reactor pit.



The <a href="https://www.earth.com/news/physicists-observe-a-new-form-of-magnetism-nil2-for-the-first-time/">magnets</a> must survive pulses lasting eight minutes and forces topping 22‑million pounds. Their success would clear one of the last engineering hurdles between experimental science and grid‑scale fusion plants.



Once stacked, the solenoid, poloidal, and toroidal coils become an electromagnetic cage surrounding fuel no heavier than a handful of hydrogen gas. 



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/superconducting-magnet_ITER-site-schematic_ITER_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/superconducting-magnet_ITER-site-schematic_ITER_1s.webp" alt="This is the ITER Tokamak Schematic. Credit: ITER Organization" class="wp-image-1977062"/></a><figcaption class="wp-element-caption">This is the ITER Tokamak Schematic. Click image to enlarge. Credit: ITER Organization</figcaption></figure>



Heating systems will raise that fuel to 270 million °F, where <a href="https://www.sciencedirect.com/topics/chemistry/atomic-nuclei" target="_blank" rel="noreferrer noopener">atomic nuclei</a> fuse and release torrents of energy.



If ITER meets its power target, it will supply data that private companies can fold into faster, cheaper reactors. Its members already share designs with startups through new tech‑transfer channels launched in 2024.



The magnet story also shows global cooperation still works. Components came from factories in the United States, China, Japan, Korea, Russia, and Europe, all machined to fit together within millimeters. 



Engineers on site say the pace has tightened their bond and sharpened methods that future plants will inherit.



<h2 class="wp-block-heading" id="h-bringing-in-private-partners">Bringing in private partners</h2>



In 2024, ITER launched an initiative to share its data and designs with private fusion companies. The goal is to speed up commercial development by offering access to research, documentation, and supply chain knowledge.



A workshop in April 2025 brought together government and industry teams to identify ways to apply ITER’s advances in real-world <a href="https://www.earth.com/news/chinas-artificial-sun-reactor-sets-new-record-for-fusion-power-generation/">reactors</a>. These partnerships are expected to lower costs, reduce risk, and shrink the timeline for bringing fusion power to the grid.



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This 3,000-ton magnet could change the future of energy forever

A 3,000‑ton stack of metal and superconducting cable is taking...

Everyone talks about mindfulness these days. People say it helps with stress, improves sleep, and makes life calmer. But here is a question: can meditation actually sharpen your focus? Turns out, it can.



A new study from the <a href="https://gero.usc.edu" target="_blank" rel="noreferrer noopener">USC Leonard Davis School of Gerontology</a> reveals something surprising: just thirty days of guided mindfulness meditation can change how quickly and accurately people focus. Age does not seem to matter here.



This is not about feelings or guesswork. Researchers used eye tracking, a tool that shows exactly where your <a href="https://www.earth.com/news/mindfulness-meditation-is-a-powerful-weapon-against-chronic-pain/">attention</a> goes. 



“This study shows that mindfulness isn’t just about feeling more relaxed - it can literally change the way your brain handles attention,” said Andy Jeesu Kim, the study’s first author. “And that’s incredibly important for maintaining cognitive health as we age.”



<h2 class="wp-block-heading" id="h-why-focus-fades-with-age">Why focus fades with age</h2>



As people get older, their brains <a href="https://www.earth.com/news/meditation-can-rapidly-reduce-ptsd-without-revisiting-trauma/">slow down</a>. They do not react as fast. Distractions take over easily.



This happens because of a brain system called the locus coeruleus–noradrenaline system. It controls attention, memory, and alertness - and it weakens with age.



Professor Mara Mather from the USC Leonard Davis School has studied this system for years. She found connections between its decline and early Alzheimer’s disease.



Earlier research hinted that mindfulness could strengthen this brain system. Meditation might boost areas that help with focus. But no one had tested this idea using precise eye-tracking methods - until now.



<h2 class="wp-block-heading" id="h-meditation-s-effect-on-focus">Meditation’s effect on focus</h2>



The researchers did not just ask people how mindful they felt. They watched their eyes when they recruited 69 people. Some were young adults. Others were middle-aged or older.



Half of the group practiced mindfulness meditation using the Headspace app. Just 10 to 15 minutes each day. The other half listened to an audiobook for the same amount of time.



Three times, participants visited the lab. They did visual tasks that measured how fast and accurately they could focus. Their eyes revealed everything. Every glance, <a href="https://www.earth.com/news/meditation-rewires-the-emotional-centers-of-the-brain/">distraction</a>, or quick decision.



<h2 class="wp-block-heading" id="h-attention-improves-with-practice">Attention improves with practice</h2>



After a month of mindfulness meditation, something changed. People began reacting faster - their eyes moved directly to the right target, they ignored distractions more easily, and it didn’t matter how old they were.



“We expected older adults to benefit the most, but we found that mindfulness improved attention similarly across young, middle-aged, and older adults,” Kim said. “This suggests mindfulness can be a useful tool at any stage of life.”



Oddly, when the participants filled out mindfulness questionnaires, their answers did not change much. They did not <a href="https://www.earth.com/news/why-meditation-and-critical-thinking-matter-in-the-age-of-ai/">feel</a> different. Their brains, however, told a different story.



<h2 class="wp-block-heading" id="h-second-test-backs-meditation">Second test backs meditation</h2>



The findings did not end there. Another study backed them up. Once again, participants practiced mindfulness meditation using Headspace for 30 days. 



The researchers tracked their eye movements while they performed attention tasks, examining both proactive focus and reactive responses. Reaction times improved again. People’s eyes became quicker - regardless of age.



However, not every gain came from meditation. Some improvements likely came from practicing the task itself. But meditation clearly sped up their visual attention.



<h2 class="wp-block-heading" id="h-meditation-works-quietly">Meditation works quietly</h2>



The second study confirmed something interesting. Meditation did not boost self-reported mindfulness. People did not feel much different.



But their eyes told a different tale. They reacted faster, spotted targets quicker, and showed subtle changes in focus.



This tells us something crucial. You might not notice the benefits of meditation right away. Yet your brain could already be working better in the background.



Both studies found that age did not limit the benefits. Young, middle-aged, or older, everyone improved.



<h2 class="wp-block-heading" id="h-sharper-focus-for-daily-needs">Sharper focus for daily needs</h2>



People often think mindfulness is just about peace and calm. But these studies reveal something bigger.



Mindfulness can sharpen the <a href="https://www.earth.com/news/action-observation-network-human-brain-perception-see-what-we-expect-to-see-mind-eye/">brain</a>’s attention. This affects everyday activities. Driving. Reading. Holding a conversation. Even crossing the street.



Sure, the audiobook group also improved a little. That is likely because they practiced the task more. But the meditation group improved faster and more clearly.



Mindfulness does not just make people feel calmer. It changes how the brain works with attention.



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



The researchers are not done yet. They want to see what happens with longer mindfulness meditation programs. Could more time bring stronger results? They are also curious whether these quick gains stick around long term.



“We’re excited about the potential of digital mindfulness interventions to help people support their brain health,” Kim said. “It’s simple, low-cost, and widely accessible. The key is consistency.”



Mindfulness may seem small. Just a few minutes a day. But it is clear. It can quietly improve your brain’s focus, no matter your age. And all it takes is a little patience and practice.



The study is published in the journal <a href="https://www.eneuro.org/content/early/2025/06/26/ENEURO.0356-23.2025" target="_blank" rel="noreferrer noopener">eNeuro</a>.



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Mindfulness meditation can rewire your brain for sharper focus

Everyone talks about mindfulness these days. People say it helps...

If you've ever forgotten to water your plants for a couple of days, you probably noticed something interesting. The flowers droop quickly. The grass gets dry. But the trees? They’re fine. 



That’s because not all plants handle water the same way. Some use water freely, while others hold back, adjusting to dry conditions in very different ways.



Yet for years, many climate models haven’t taken those differences into account. They’ve relied on simple assumptions that treat every plant alike. That may soon change, thanks to new research that puts plant behavior into the equation.



<h2 class="wp-block-heading" id="h-climate-model-gets-plant-upgrade">Climate model gets plant upgrade</h2>



Scientists from <a href="https://www.ucsb.edu/">UC Santa Barbara</a> and San Diego State University have built a better way to look at how soil dries out after rain. 



Their model shows that plants don’t follow a one-size-fits-all response to water stress. Instead, they behave in complex, adaptive ways - something the researchers say could help sharpen predictions about climate, weather, and water use.



Kelly Caylor, a professor at UCSB’s Bren School of Environmental Science &amp; Management, is the senior author of the study.



“We found that plants don't respond to water stress in a simple, straight-line way,” she said. “Instead, they have dynamic response patterns that reveal whether they're ‘water spenders’ or ‘water savers.’”



<h2 class="wp-block-heading" id="h-where-rainwater-really-goes">Where rainwater really goes</h2>



After it rains, water goes in a few directions. Some of it runs off into rivers. Some seeps down into the ground. 



The rest goes back up into the air - either by evaporating or by moving through plants, which release water through their leaves in a process called transpiration. Together, these are known as <a href="https://www.earth.com/earthpedia-articles/water-cycle/">evapotranspiration</a>.



How quickly soil dries out affects everything from crop growth to wildfire risk to weather forecasts. But until recently, scientists didn’t have good large-scale data on how this drying process worked. Instead, they built models based mostly on rainfall and streamflow.



“Ironically, most models do not use soil moisture data, although the soil moisture is a central component to hydrological behavior,” said lead author Ryoko Araki, a joint doctoral student at UCSB and SDSU.



<h2 class="wp-block-heading" id="h-plants-respond-in-unique-ways">Plants respond in unique ways</h2>



Until now, even the more advanced models made a big assumption: that all plants slow down their water use in the same way, at the same rate, under the same conditions.



“All plants - no matter young or old, summer or winter, tree or grass, small or large,” Araki said. But that assumption skips over a critical part of the picture. Different plants behave differently under <a href="https://www.earth.com/news/plants-have-a-secret-weapon-for-surviving-stress/">stress</a>.



By ignoring that, the models miss out on useful clues. So Araki and her colleagues wondered - could a nonlinear model, one that accounts for more complex plant responses, offer better insights?



<h2 class="wp-block-heading" id="h-a-smarter-way-to-model-moisture">A smarter way to model moisture</h2>



The team began with a standard, linear model based on time and moisture levels. Then they added a nonlinear factor that could reflect how plants adjust their water use as conditions change.



One thing that set this project apart was the data. The scientists used information from NASA’s SMAP satellite, which tracks <a href="https://www.earth.com/news/how-soil-moisture-can-predict-severe-storms/">soil moisture</a> across the globe using microwave sensors. That gave them a way to test their model against real-world conditions.



And it worked. The nonlinear model outperformed the two most widely used linear models. The older models tended to overestimate how fast soil dries out. That can lead to bad predictions—especially in regions where water supply is already tight.



Still, not everyone in the field is on board. Some researchers say the added complexity isn’t worth the trouble.



“Even though the nonlinear model is more complicated, it fits the data better, and it captures more of the system’s behaviors,” Araki said. “It provides a way to investigate <a href="https://www.earth.com/news/how-plants-adapt-to-survive-a-changing-climate/">plant adaptations</a>.”



<h2 class="wp-block-heading" id="h-watching-plants-work-from-space">Watching plants work, from space</h2>



There’s no easy way to track how individual plants manage water stress. You can’t just walk into a forest and see whether a tree is slowing down its water use or pushing forward through dry soil.



“Do they keep growing as much as they can while they still have some amount of water, or do they just completely stop transpiring to prevent tissue damage?” said co-author Bryn Morgan, a former UCSB doctoral student who is now a postdoctoral fellow at MIT.



That’s why this model matters. It gives scientists a window into plant behavior on a massive scale. It also shows that there’s more going on beneath the surface - literally - than many models have accounted for.



For <a href="https://www.earth.com/news/gardeners-can-make-small-changes-to-benefit-pollinators/">gardeners</a>, farmers, and anyone keeping an eye on climate trends, this kind of research could lead to better tools and smarter predictions. Because as it turns out, understanding how a tree survives a dry spell might help all of us prepare for what’s ahead.



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Not all plants handle water the same - here’s why it matters

If you've ever forgotten to water your plants for a...

A new 3D simulation tool is helping scientists better predict landslides, rockfalls, and avalanches in the Alps - a region with steep, unpredictable terrain packed with ice, snow, and rock. These conditions have long made hazard forecasting extremely difficult.



Scientists at <a href="https://ethz.ch/en.html">ETH Zurich</a> and the WSL Institute for Snow and Avalanche Research (SLF) have built a model that can better simulate how these massive natural movements unfold. And it just passed its first real-world test: the evacuation of the village of Brienz in 2023.



<h2 class="wp-block-heading" id="h-simulating-avalanches-in-3d">Simulating avalanches in 3D</h2>



Until recently, most simulations used to forecast mass movements relied on 2D, depth-averaged models. These methods estimate average flow direction, speed, and thickness. They’re fast and helpful for general risk estimates, but their usefulness declines in rugged, highly variable landscapes.



“While classical depth-averaged models are very useful for first-order estimates, many have difficulties when dealing with rugged, irregular terrain like that seen in <a href="https://www.earth.com/news/glacier-collapse-buried-a-village-in-the-swiss-alps/">Blatten</a>, where flow behavior is highly three-dimensional,” explained Professor Johan Gaume of ETH Zurich and SLF.



In 2022, he and his team published a paper outlining a new 3D avalanche model aimed at solving this problem. They accurately recreated several well-known disasters after the fact, including the 2017 Piz Cengalo rock-ice avalanche and the 1963 Vajont landslide.



But those were all simulations run after the events had happened. The real test would be to predict an event before it occurred.



<h2 class="wp-block-heading" id="h-avalanche-prediction-proved-accurate">Avalanche prediction proved accurate</h2>



In spring 2023, the mountainside above Brienz began to shift. Authorities ordered an evacuation. Without tweaking their model or adjusting any parameters, the ETH and SLF team ran what they called "blind simulations."



They used surface movement data and conservative estimates from rock lab tests to gauge how much mass might fall and how it would move. 



“Our simulation predicted that the resulting avalanche would stop just tens of meters short of the first houses. These results were shared informally with cantonal authorities and ultimately matched the actual extent of the real landslide very closely,” Gaume said.



<h2 class="wp-block-heading" id="h-a-tougher-avalanche-simulation">A tougher avalanche simulation</h2>



In May 2025, a new risk appeared. This time, it was the village of Blatten. The hazard was even greater, involving a mix of rock, <a href="https://www.earth.com/news/secrets-of-snow-complexity-can-improve-winter-safety/">snow</a>, and glacier ice from the Birch Glacier. 



Once again, the ETH and SLF team jumped into action. They weren’t officially commissioned and had no direct contact with authorities, but they saw an opportunity to test their avalanche model against a much more complex challenge.



“Given the dramatic situation in Blatten and the novelty of our modeling approach, we proceeded with great caution and subjected the model to a rigorous verification process to ensure its accuracy and reliability,” Gaume said.



They estimated that the falling mass could be around 10 million cubic meters - a mix of 3 to 5 million cubic meters of rock and 5 million cubic meters of glacier ice. That estimate later proved extremely accurate: a post-event analysis confirmed a total of 9.3 million cubic meters.



For the sliding friction, they used a coefficient of 0.2 - a cautious pick based on past events. Though later tests suggested 0.23 would have been even closer to the final outcome, the match between simulation and reality was striking.



<h2 class="wp-block-heading" id="h-3d-shows-avalanche-shockwaves">3D shows avalanche shockwaves</h2>



Most standard tools in hazard modeling assume the mass always stays in contact with the ground, sliding along the surface. But in Blatten, part of the avalanche flow shot into the air. That “airborne phase” created shockwaves and debris that flew over 100 meters above the terrain. The ETH-SLF model captured that too.



“In contrast, our 3D model allows particles to detach from the surface, reducing ground friction and accurately capturing airborne phases - this is critical for simulating flow behavior and runout in steep or complex terrain,” said Gaume.



The simulation showed a runout of 1.2 kilometers on the southwest valley wall and 700 meters on the northeast side. Those numbers almost exactly matched what actually happened. Most of Blatten was destroyed. Weissenried, nearby, was spared by a narrow margin.



<h2 class="wp-block-heading" id="h-making-the-tool-widely-usable">Making the tool widely usable</h2>



The ETH and SLF researchers are working to make their 3D tool for avalanches accessible to officials and engineers.



“Our aim is not to replace existing 2D tools, but to offer a complementary solution where classical models may reach their limits. We are actively working to make our model accessible and usable for practitioners and authorities,” says Gaume.



The team emphasized that their simulations were not officially part of the risk management process in Blatten. But the results speak for themselves. They show how much more accurate hazard <a href="https://www.earth.com/news/bridging-the-gap-the-quest-for-accurate-weather-forecasts/">forecasts</a> could become.



“We now have a reliable, ready-to-use tool that enables us to support the authorities with simulations assessing the potential consequences of impending mass movements,” said Gaume.



<h2 class="wp-block-heading" id="h-respect-for-lives-and-limits">Respect for lives and limits</h2>



Gaume expressed his respect for the way local officials handled the crisis, praising authorities in the Lötschental and in Brienz for their exemplary management and expressing deep compassion for residents who lost their homes and belongings.



“Tragically, the glacier collapse also claimed one life, which reminds us of the very real human cost behind these <a href="https://www.earth.com/news/natural-disasters-are-on-the-rise-but-hazard-plans-are-inadequate/">natural disasters</a>,” he said.



Looking back, Gaume remembers feeling unsure of the predictions. “The initial results I obtained seemed rather unrealistic, particularly due to the significant upslope flow toward Weissenried."



"Had I had the opportunity to visit the site before running the simulation, I would likely have found these results even less plausible, given the elevation of the village relative to the Lonza," he said. "I therefore felt it was essential to discuss them with my colleagues before taking any more formal steps.”



With continued refinement and real-world testing, this new 3D model may help save lives and minimize damage in future avalanches. It marks a shift in how we understand and respond to complex alpine hazards -with more accuracy, humility, and responsibility.



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Breakthrough model will transform avalanche prediction

A new 3D simulation tool is helping scientists better predict...

Lakes are lifelines across the world - storing water, sheltering diverse wildlife, and supporting millions of people. But today, these vital ecosystems are facing a growing threat that could upend the balance they have long sustained.



Climate change is putting pressure on these <a href="https://www.earth.com/news/climate-shock-lakes-are-losing-oxygen-faster-than-expected/">water</a> bodies. Scientists want to know whether lakes rely more on rain or groundwater. This information can help protect lakes from water stress during droughts.



In a new study, researchers collected data from 350 lakes in 18 European countries. They studied how these lakes react to climate shifts.



The team presented their findings at the <a href="https://conf.goldschmidt.info/goldschmidt/2025/meetingapp.cgi" target="_blank" rel="noreferrer noopener">Goldschmidt Conference</a> in Prague. Their results show why every drop of water counts.



<h2 class="wp-block-heading" id="h-sources-of-lake-water">Sources of lake water</h2>



Researchers at the <a href="https://www.avcr.cz/en/" target="_blank" rel="noreferrer noopener">Czech Academy of Sciences</a> used hydrogen and oxygen isotopes, called 18O and 2H, to study the lakes.



The isotopes reveal how much water comes from rain and how much from underground <a href="https://www.earth.com/news/lakes-are-warming-toward-the-point-of-no-return/">sources</a>. They also show how much water is lost through evaporation.



The researchers gathered data on weather, land use, and lake characteristics. They looked at temperature, rainfall, humidity, forests, farms, and even city areas near lakes.



The data was combined using machine learning, which allowed the experts to identify patterns and predict future risks for the lakes.



<h2 class="wp-block-heading" id="h-groundwater-provides-more-stability">Groundwater provides more stability</h2>



Lakes fed by groundwater proved to be more resilient, maintaining steady water levels even during dry spells. 



In contrast, shallow lakes were far more vulnerable. With their broad surfaces, they lose <a href="https://www.earth.com/news/earths-oceans-are-rapidly-changing-colors-matching-climate-predictions/">water</a> rapidly through evaporation and have little ability to replenish it. 



The study warns that as temperatures continue to rise, these shallow lakes could face increasingly severe challenges.



<h2 class="wp-block-heading" id="h-lowland-lakes-face-high-risks">Lowland lakes face high risks</h2>



Lakes in lowland areas face greater danger. The study predicts that many of these lakes will face critical water loss by 2050.



Artificial lakes, like reservoirs, face the biggest <a href="https://www.earth.com/news/underground-lake-capable-of-filling-three-and-a-half-olympic-swimming-pools/">risks</a>. They are often shallow and lack strong groundwater connections.



Many of these lakes also sit in farming regions. Fertilizers and other chemicals from farms often wash into them, harming water quality. This creates both pollution and water shortage risks.



<h2 class="wp-block-heading" id="h-mountain-lakes-are-more-stable">Mountain lakes are more stable</h2>



Lakes at high altitudes are currently more resilient. Cooler temperatures help lower evaporation rates. Groundwater connections in these lakes are often stronger.



High-altitude lakes also largely avoid pollution, at least for now. Most are far from intensive farming areas. However, that could change soon.



Farming is slowly expanding into higher areas. This could bring new pollution risks to mountain lakes in the future.



<h2 class="wp-block-heading" id="h-different-strategies-are-needed">Different strategies are needed</h2>



At the conference, Dr. Cristina Paule-Mercado from the <a href="https://www.avcr.cz/cs/" target="_blank" rel="noreferrer noopener">Czech Academy of Sciences</a> explained the study results. She noted that her team initially expected the same controlling factors to apply across all lakes, but that wasn't the case. 



"While we can draw some general insights from the analysis, we also observed how each region has different dynamics driven by the interaction of multiple variables," said Dr. Paule-Mercado.



"This highlights the importance of considering all these factors - and particularly groundwater-lake connectivity - when designing sustainable management strategies to address climate change and water scarcity."



<h2 class="wp-block-heading" id="h-protecting-lakes-from-water-stress">Protecting lakes from water stress</h2>



The study has not ended here. In fact, it has just started growing. The research team is expanding their work to include over 400 lakes across different regions.



The main goal is to build a global database of lakes and water systems. This database will help track changes and guide future water protection efforts.



The researchers draw on a wide range of data sources, including open-access databases that provide freely available information. They also conduct fieldwork, visiting lakes in person to collect fresh water samples for detailed analysis.



The project has grown into a truly collaborative effort. Scientists from around the world are now contributing, and local communities are playing an active role. 



Citizen science has also become a big part of the research, with residents living near the lakes helping to collect data and monitor water conditions firsthand. 



By combining all these efforts, the team hopes to protect lakes from water stress and improve management for communities worldwide.



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Why some lakes may disappear faster than others

Lakes are lifelines across the world - storing water, sheltering...

Yellow,Baltic,Amber,Stones,Among,The,Sand,And,Seashells,Close

A layer of fossilized resin, known as amber, sits in deep‑sea clay and has puzzled geologists for decades. New fieldwork in northern Japan now shows that a tsunami powerful enough to rip coastal forests from their roots hurled that resin into 11,000‑foot‑deep water during the age of the dinosaurs.



Aya Kubota of the <a href="https://www.gsj.jp/en/" target="_blank" rel="noreferrer noopener">Geological Survey of Japan</a>, and her team, traced the resinous material to a 115‑million‑year‑old horizon in Hokkaido’s Shimonakagawa Quarry, matching it to tsunami‑generated <a href="https://ui.adsabs.harvard.edu/abs/2013AGUFMNH51D..01N/abstract" target="_blank" rel="noreferrer noopener">turbidites</a>.



<h2 class="wp-block-heading" id="h-tracing-the-tree-resin-trail">Tracing the tree resin trail</h2>



Tree resin oozes from bark, traps insects, and usually hardens on a forest floor. Geochemical clocks show that transformation from sticky resin to rock takes at least two million years, yet the Shimonakagawa specimens were still pliable when buried.



Modern tests confirm that resin exposed to air stiffens within about a week, while resin that hits <a href="https://www.pnas.org/doi/10.1073/pnas.0707949104" target="_blank" rel="noreferrer noopener">water</a> can stay soft for much longer. 



That simple fact let the team work backward, proving that the resin reached the seabed almost immediately after leaving the trees.



“As resin exposed to the air hardens quickly in weeks, the flame deformation of the resin suggests that it reached <a href="https://oceanservice.noaa.gov/facts/pelagic.html" target="_blank" rel="noreferrer noopener">pelagic seafloors</a> without significant subaerial exposure,” wrote Kubota and colleagues. 



Those flame structures, familiar to sedimentologists who study load deformities, appear in the amber exactly where dense sand slumped beneath lighter resin.



<h2 class="wp-block-heading" id="h-testing-a-tsunami-hypothesis">Testing a tsunami hypothesis</h2>



<a href="https://www.earth.com/news/90-million-year-old-amber-reveals-antarcticas-secret-past/">Amber</a> occurs in thirty stacked beds within the quarry, some only two inches thick and others nearly nine feet, yet every layer sits above calm‑water clay. 



Storm waves cannot reach such depths, and river floods leave different grain patterns, so the researchers looked to colossal waves.



“Tsunami <a href="https://www.earth.com/news/650-foot-mega-tsunami-sends-seismic-waves-around-world-dickson-fjord-swot-mission/">deposits</a> are rarely recognized in the geological record, except for geologically young Holocene coastal deposits,” the team added. That scarcity makes each confirmed paleotsunami layer a treasure trove for hazard models.



The tallest tsunami measured in modern times reached <a href="https://www.wired.com/2009/07/dayintech-0709" target="_blank" rel="noreferrer noopener">1,720 ft</a> (524 meters) in Alaska’s Lituya Bay in 1958. Even a smaller wave, crossing the ancient Northwest Pacific, could have torn out whole stands of conifer, rafted them far offshore, and dumped their resin as the water retreated.



<h2 class="wp-block-heading" id="h-clues-locked-in-deep-sea-mud">Clues locked in deep‑sea mud</h2>



Besides <a href="https://www.earth.com/news/parasitic-wasp-had-a-flytrap-for-snatching-its-victims/">amber</a>, the Japanese cores contain coffee‑table‑sized rip‑up clasts, broken driftwood more than four feet (1.2 meters) long, and tangled mats of leaves. Each item points to sudden, violent transport from land to abyss rather than slow settling.



Mud cracks on some clasts close upward, showing they dried in air before the wave plucked them from coastal flats. 



Microscopic study reveals intact pollen inside the resin, supporting the idea of a rapid ride that spared delicate grains from decay.



Soft‑sediment folds wrap around still‑elastic resin sheets, confirming that the tsunami‑<a href="https://www.earth.com/news/mega-tsunamis-triggered-by-earthquakes-could-wipe-part-of-us-off-the-map/">triggered</a> slurry flowed over an already mobile seafloor. 



Those folds help explain why the amber sheets resemble squeezed taffy rather than neat droplets.



<h2 class="wp-block-heading" id="h-tsunami-linked-to-massive-landslide">Tsunami linked to massive landslide</h2>



Hokkaido straddles four converging <a href="https://www.earth.com/news/earth-only-has-six-continents-not-seven-tectonic-plates-under-iceland-study/">tectonic plates</a> today, and plate reconstructions indicate a similar geometry in the <a href="https://www.nhm.ac.uk/discover/the-cretaceous-period.html" target="_blank" rel="noreferrer noopener">Early Cretaceous</a>. 



Kubota’s group links the tsunami to a massive landslide that detached a shallow‑marine carbonate platform some 125 miles (200 kilometers) south of the quarry.



Zircon dating of volcanic ash bracketing the amber shows the catastrophe struck between 116.8 million and 114.8 million years ago. 



That window overlaps an interval of heightened plate re‑organization as the <a href="https://www.sciencedirect.com/science/article/pii/S0012821X22000814" target="_blank" rel="noreferrer noopener">Izanagi‑Kula oceanic plate</a> subducted beneath eastern Asia.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/tsunami_swept_amber_tree-resin_forest-to-seabed_illustration_credit-GSJ_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/tsunami_swept_amber_tree-resin_forest-to-seabed_illustration_credit-GSJ_1s.webp" alt="Reconstruction of Early Cretaceous large-scale tsunamis which reached pelagic deep-sea bottoms from lands. (1) Outbreaks of earthquakes and tsunamis. (2) Destruction of extensive forests and seafloors by tsunamis and (3) Discharge of numerous fresh resin, plant debris and siliciclastic sediments into the ocean. (4) Direct and rapid transportation into deep sea bottoms by tsunami-induced turbidity currents. (5) Wood and resin drift and (6) late settling. (7) Repeated tsunamis during tectonic instability, and (8) its archives in pelagic strata. Credit: Geological Survey of Japan" class="wp-image-1976964"/></a><figcaption class="wp-element-caption">Reconstruction of Early Cretaceous large-scale tsunamis which reached pelagic deep-sea bottoms from lands. (1) Outbreaks of earthquakes and tsunamis. (2) Destruction of extensive forests and seafloors by tsunamis and (3) Discharge of numerous fresh resin, plant debris and siliciclastic sediments into the ocean. (4) Direct and rapid transportation into deep sea bottoms by tsunami-induced turbidity currents. (5) Wood and resin drift and (6) late settling. (7) Repeated tsunamis during tectonic instability, and (8) its archives in pelagic strata. Click image to enlarge. Credit: Geological Survey of Japan</figcaption></figure>



Comparable offshore evidence exists elsewhere, including sediment cores that record the 365 CE <a href="https://www.nature.com/articles/s41598-022-09058-3" target="_blank" rel="noreferrer noopener">Crete megatsunami</a> across the Mediterranean basin. 



Those parallels strengthen the idea that deep‑water archives can outlast coastal erosion and preserve tsunami fingerprints for tens of millions of years.



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



Today’s engineers map 500‑year floodplains but rarely factor in events of the magnitude inferred at Shimonakagawa. 



Kubota’s discovery shows that extreme waves can move entire forests and carve fresh sediment routes to the deep ocean.



By recognizing amber as a tsunami <a href="https://www.earth.com/news/scientists-detect-a-rare-slow-motion-earthquake-along-japans-tsunami-fault/">tracer</a>, scientists gain a fresh tool for spotting ancient coastal disasters on continental margins worldwide. 



Each new data point refines recurrence estimates and could, eventually, guide zoning in quake‑prone regions.



Forest‑derived carbon delivered to the abyss also hints at hidden climate feedbacks, because buried wood removes atmospheric CO₂ for geologic time. 



Understanding that sink requires knowing how often tsunamis act as high‑speed conveyors from land to sea.



Researchers now plan to scan other Cretaceous drill cores for thin orange films that might mark overlooked tsunami horizons. Success could turn a onetime curiosity into a standard indicator for ancient coastal risk.



Full details of the study are published in the journal <a href="https://www.nature.com/articles/s41598-025-96498-2" target="_blank" rel="noreferrer noopener">Nature</a>.



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Massive tsunami swept tree resin and amber from an inland forest out into the seabed

A layer of fossilized resin, known as amber, sits in...

Pollinators are vital for the natural world. They help plants reproduce, support food webs, and sustain ecosystems. Among them, honey bees hold a special place. 



Honey bees are widely celebrated for their role in agriculture and are often seen as environmental heroes. However, their growing presence in places where they are not native raises new concerns.



Southern California is a well-known biodiversity hotspot. It is home to hundreds of native pollinator species. But this unique region now faces a quiet threat. 



Feral honey <a href="https://www.earth.com/news/world-bee-day-2025-protecting-the-pollinators-that-feed-the-world/">bees</a>, thriving outside human control, have begun to dominate pollination networks here. Their influence extends far beyond what most people realize.



A new study from <a href="https://ucsd.edu" target="_blank" rel="noreferrer noopener">University of California San Diego</a> sheds light on this issue. The research uncovers how honey bees, despite their benefits, may unintentionally harm native pollinators. The findings challenge common perceptions and bring attention to a growing ecological conflict.



<h2 class="wp-block-heading" id="h-honey-bees-outcompete-native-pollinators">Honey bees outcompete native pollinators </h2>



Honey bees are highly effective <a href="https://www.earth.com/news/how-bumble-bees-are-sabotaging-their-own-health/">pollinators</a>. They have been introduced worldwide to support crop production. In the U.S., they are responsible for pollinating crops that contribute billions of dollars to the economy each year.



Their ability to communicate allows them to locate and exploit floral resources efficiently. They share information about flower locations with their colony mates, which makes them powerful foragers. Unlike most native bees, honey bees live in large colonies that work together to gather resources.



Because of their efficiency, honey bees outcompete many native bees. They can strip flowers of pollen and nectar quickly. 



Studies show that in Southern California, honey bees now represent nearly 90% of all bees visiting flowers. This leaves little for the region’s diverse native bee <a href="https://www.earth.com/news/rising-dangers-threaten-the-survival-of-bees-and-pollinators/">species</a>, which rely on the same resources.



<h2 class="wp-block-heading" id="h-scale-of-the-honey-bee-invasion">Scale of the honey bee invasion</h2>



The study found that honey bees now make up 98% of total bee biomass in Southern California’s scrublands. This is not just about numbers. Honey bees are much larger than most native bees in this region. Their dominance extends both in terms of individuals and body size.



One reason for this imbalance is the honey bees' remarkable ability to remove pollen. The research showed that honey bees can remove up to 80% of pollen from flowers within just one day. 



In experiments, just two visits by honey bees stripped over 60% of pollen from flowers of native plants like black sage, white sage, and distant phacelia.



Such high pollen removal rates mean that other bees have far fewer resources left. Native <a href="https://www.earth.com/news/native-bee-species-face-extinction-due-to-honey-bee-competition/">bees</a>, many of which are solitary and less efficient foragers, simply cannot compete at this scale.



<h2 class="wp-block-heading" id="h-honey-bees-and-pollen-resources">Honey bees and pollen resources </h2>



Pollen is critical for bee reproduction. Bees collect pollen to feed their larvae. When honey bees take most of the pollen, native bees struggle to raise their young.



The study estimated the daily impact of honey bees on pollen resources. In one hectare of habitat, honey bees removed enough pollen each day to potentially raise hundreds to thousands of native bees. 



Over an entire bloom season, this could result in the loss of tens of thousands of potential native bee offspring.



This finding is alarming. It highlights how honey bees, though often viewed positively, may reduce native bee populations by monopolizing food sources.



<h2 class="wp-block-heading" id="h-larger-bees-face-greater-risks">Larger bees face greater risks</h2>



Interestingly, larger native bees appear to be most affected. The study found that only a tiny fraction of native bees were larger than honey bees. Bumble bees, for instance, made up just 0.1% of all bees observed.



Larger bees generally require more pollen to raise their offspring. When honey bees deplete resources, these species may be pushed out first.



“Although honey bees are rightly considered an indispensable asset to humans, they can also pose a serious ecological threat to natural ecosystems where they are not native,” said Hung.



The loss of large bees could also reduce the effectiveness of pollination. These bees tend to carry more pollen per visit, which benefits many plants.



<h2 class="wp-block-heading" id="h-honey-bees-vs-native-pollinators">Honey bees vs. native pollinators</h2>



The damage does not stop with bees. The study also highlights that honey bee pollination leads to poorer plant offspring quality compared to native bee pollination.



This happens because honey bees often visit many flowers on the same plant before moving to another. This behavior increases the chances of self-pollination, which can lead to inbreeding depression in plants.



Such effects could ripple through ecosystems. Plants that rely on native bees for effective pollination may see lower reproduction rates. This could further degrade habitats that native bees and other wildlife depend on.



<h2 class="wp-block-heading" id="h-the-spread-of-feral-honey-bees">The spread of feral honey bees </h2>



Feral honey bee colonies are not just an issue in Southern California. These bees have spread worldwide and often outnumber managed colonies.



They thrive in many ecosystems and are difficult to remove once established. Unlike managed bees, feral colonies are self-sustaining and active year-round.



The study points out that feral honey bees have even replaced native bees in other regions. In the southwestern United States, they are increasingly common on both abundant and rare plants.



<h2 class="wp-block-heading" id="h-rethinking-conservation-priorities">Rethinking conservation priorities</h2>



Many people remain unaware of the negative effects of honey bees on native wildlife. Public concern tends to focus on protecting honey bees from disease and habitat loss.



Yet, the study’s authors warn that in North America, honey bees often act as competitors, not conservation targets.



“The plight of the honey bee is an issue of animal husbandry and livestock management, whereas when it comes to conservation issues here in North America, honey bees are likelier to be part of the problem, not a solution or a target for conservation,” said Hung.



This statement challenges common assumptions. It suggests a need for more balanced conservation strategies that consider native pollinators too.



<h2 class="wp-block-heading" id="h-steps-toward-potential-solutions">Steps toward potential solutions</h2>



Managing honey bee populations in sensitive areas may help. The researchers suggest limiting commercial beekeeping on public lands after crop blooms end.



“In areas with threatened bee species, natural preserve managers may also want to consider systematic removals or relocations of non-native honey bee colonies to provide wild bees a fighting chance,” said Hung.



Though such measures may seem extreme, they are not unprecedented. Many conservation programs already target invasive species to protect native wildlife.



<h2 class="wp-block-heading" id="h-honey-bees-harming-native-life">Honey bees harming native life</h2>



The study reveals a hidden layer of the pollination crisis. Honey bees, often seen as ecological heroes, can create serious problems in certain ecosystems.



As more people become aware of this issue, discussions around pollinator conservation may shift. Future efforts must balance the needs of agriculture with the importance of protecting native species.



The story of honey bees in Southern California serves as a reminder. Even well-known species can become a threat when removed from their native contexts.



Protecting biodiversity requires seeing the full picture, even when it challenges popular beliefs.



The study is published in the journal <a href="https://resjournals.onlinelibrary.wiley.com/doi/10.1111/icad.12858" target="_blank" rel="noreferrer noopener">Insect Conservation and Diversity</a>.



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Honey bee invasion: A growing threat to native pollinators

Pollinators are vital for the natural world. They help plants...

Coral reefs are in trouble. As oceans warm and environments shift, the vibrant ecosystems built by corals are turning pale and dying off. 



While scientists have known for years that coral bleaching is linked to the loss of symbiotic algae, they’ve never been able to watch the process unfold at the cellular level in realtime - until now.



<h2 class="wp-block-heading" id="h-underwater-microscope-for-studying-coral">Underwater microscope for studying coral</h2>



Researchers at the <a href="https://scripps.ucsd.edu/">Scripps Institution of Oceanography at UC San Diego</a> have created a handheld underwater microscope. The device makes it possible to study coral photosynthesis right where it happens - in the ocean, inside living coral tissue - without causing any damage.



The team named the device the Benthic Underwater Microscope imaging PAM - BUMP, for short.



The Jaffe Lab for Underwater Imaging at Scripps Oceanography built the microscope with support from the U.S. National Science Foundation.



The tool combines imaging with a light-based technique known as pulse amplitude modulated (PAM) fluorometry to measure how efficiently tiny algae inside corals are <a href="https://www.earth.com/news/the-fate-of-coral-reefs-lies-in-the-hands-of-their-tiny-inhabitants/">photosynthesizing</a>.



<h2 class="wp-block-heading" id="h-coral-depends-on-glowing-algae">Coral depends on glowing algae</h2>



The algae, called <a href="https://www.earth.com/news/symbiosis-will-help-some-corals-survive-in-a-warming-world/">symbionts</a>, are essential for coral survival. They live within coral tissue and convert sunlight, water, and carbon dioxide into sugars and oxygen.



The coral, in turn, uses that energy to grow and build reefs. But when stressed by warming seas or pollution, corals eject these algae. Without them, corals appear white and slowly starve - known as the bleaching effect.



The BUMP microscope makes it possible to monitor this relationship in real-time and in natural environments - something that couldn’t be done before.



<h2 class="wp-block-heading" id="h-a-huge-technological-leap">A huge technological leap</h2>



“This microscope is a huge technological leap in the field of coral health assessment,” said study lead author Or Ben-Zvi, a postdoctoral researcher at Scripps Oceanography. 



“Coral reefs are rapidly declining, losing their photosynthetic symbiotic algae in the process known as <a href="https://www.earth.com/news/the-worlds-largest-coral-bleaching-event-is-now-underway/">coral bleaching</a>."



"We now have a tool that allows us to examine these microalgae within the coral tissue, noninvasively and in their natural environment.”



The microscope is small enough to fit in a carry-on suitcase. It’s light enough for a diver to bring to the seafloor without a ship’s help. 



Controlled with a touchscreen and powered by a battery pack, the microscope uses focused LED lights and high-magnification lenses to capture vivid images and videos. It also creates detailed 3D scans and maps photosynthesis in high resolution.



<h2 class="wp-block-heading" id="h-microscope-reveals-corals-inner-glow">Microscope reveals corals’ inner glow</h2>



At just 10 micrometers wide - one-tenth the width of a human hair - coral symbionts are invisible to the naked eye. But when corals are viewed under the microscope, the <a href="https://www.earth.com/news/marine-algae-genes-chlorophyll-boost-crop-yields-land-plants/">algae</a> glow red due to chlorophyll, the pigment that powers <a href="https://www.earth.com/news/key-to-life-on-earth-photosynthesis-begins-on-the-quantum-level-with-a-single-photon/">photosynthesis</a>. 



PAM technology measures this glow to calculate how efficiently the algae are converting light into energy. Other glowing areas, like cyan and green patches, come from fluorescent proteins that the coral produces, often around its mouth and tentacles. 



The images help researchers “see” coral health without touching or harming them. "We get a lot of information about their health without the need to interrupt nature,” said Ben-Zvi. 



“It's similar to a nurse who takes your pulse and tells you how well you're doing. We're checking the coral's pulse without giving them a shot or doing an intrusive procedure on them.”



<h2 class="wp-block-heading" id="h-observing-corals-at-unseen-scales">Observing corals at unseen scales</h2>



Ben-Zvi and her colleagues tested the microscope at coral hotspots around the world - including Hawaii, the Red Sea, and <a href="https://www.earth.com/news/coral-reefs-in-some-parts-of-the-world-actually-benefit-from-warming-el-nino-events/">Palmyra Atoll</a> - in collaboration with the Smith Lab at Scripps Oceanography. 



What they saw surprised them. Corals weren’t passive. They moved constantly, changing shape, reacting to particles, and even behaving in ways that looked like fighting or kissing.



Ben-Zvi observed coral polyps contracting their tentacles, possibly trying to remove or capture something floating by.



“The more time we spend with this microscope, the more we hope to learn about corals and why they do what they do under certain conditions,” she said. 



“We are visualizing photosynthesis, something that was previously unseen at the scales we are examining, and that feels like magic.”



<h2 class="wp-block-heading" id="h-early-detection-of-coral-stress">Early detection of coral stress</h2>



Corals face serious threats from climate change, and once bleaching begins, it can be hard to stop. But this microscope might help researchers catch problems earlier.



“The microscope facilitates previously unavailable, underwater observations of <a href="https://www.earth.com/news/what-grazing-halos-and-parrotfish-reveal-about-coral-reef-health/">coral health</a>, a breakthrough made possible thanks to the National Science Foundation and its critical investment in technology development,” said Jules Jaffe, a research oceanographer at Scripps and co-author of the study. 



Without continued federal funding, scientific research is at risk. In this case, however, support from <a href="https://www.nsf.gov/">NSF</a> enabled the team to build a device that helps solve the physiological mystery of coral bleaching and, ultimately, inform efforts to reverse it.



By detecting signs of stress before the coral reaches the tipping point, the researchers hope to create better strategies for protecting reefs from events like marine heatwaves.



<h2 class="wp-block-heading" id="h-studying-kelp-and-ocean-algae">Studying kelp and ocean algae</h2>



The potential doesn’t stop with corals. Scientists at Scripps Oceanography are already using the BUMP microscope to study other tiny marine life that rely on photosynthesis, including baby kelp off the coast of California.



“Since photosynthesis in the ocean is important for life on earth, a host of other applications are imaginable with this tool, including right here off the coast of San Diego,” said Jaffe.



In short, the BUMP microscope gives scientists something they’ve never had before: a new way to look at life underwater - close up, in motion, and alive. And with this new perspective, scientists are hoping to find better ways to protect some of the most fragile ecosystems on the planet.



The full study was published in the journal <a href="https://besjournals.onlinelibrary.wiley.com/doi/10.1111/2041-210X.70078">Methods in Ecology and Evolution</a>.



About the image: The photo features the coral&nbsp;Stylophora pistillata&nbsp;taken with the new micrsope, BUMP. Each polyp has a mouth and a set of tentacles, and the red dots are individual microalgae residing inside the coral tissue. Credit: Or Ben-Zvi



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Microscope reveals coral health in unprecedented detail

Coral reefs are in trouble. As oceans warm and environments...

Indian,Senior,Woman,Have,Sensitive,Teeth,With,Ice,Lolly,Or

For most of us, teeth mean crunching pretzels or tearing steak. But a new fossil analysis suggests their first job was feeling the world, not shredding it.



“What good is having all these teeth on the outside?” asked Yara Haridy of the <a href="https://www.uchicago.edu/en" target="_blank" rel="noreferrer noopener">University of Chicago</a>, lead author of the study. Using high‑energy scans, researchers found that the earliest tooth‑like bumps sat on fish skin and were wired for sensation.&nbsp;



<h2 class="wp-block-heading" id="h-teeth-began-as-skin-sensors">Teeth began as skin sensors</h2>



These skin teeth, known as <a href="https://www.morphosource.org/projects/000626244" target="_blank" rel="noreferrer noopener">odontode units</a>, appear in Eriptychius fossils from the middle <a href="https://ucmp.berkeley.edu/ordovician/ordovician.php" target="_blank" rel="noreferrer noopener">Ordovician Period</a>, roughly 460 million years ago. 



Slicing the fossils reveals thick bands of <a href="https://www.drbicuspid.com/clinical/imaging-cad-cam/article/15747523/fossil-scans-of-ancient-fish-may-explain-modernday-tooth-sensitivity" target="_blank" rel="noreferrer noopener">dentine</a>, the same pain‑transmitting material that still lies beneath human enamel.



Each odontode contains a pulp <a href="https://www.earth.com/news/tooth-enamel-analysis-suggests-early-eurasians-were-multiple-species-paranthropus-robustus/">cavity</a> and wide tubules that open at the surface, a layout ideal for detecting pressure or temperature shifts. By contrast, later fish with heavy enamel caps muted that sensitivity but gained better protection.



One celebrated Cambrian candidate for the “first fish,” Anatolepis, has been demoted after fresh scans showed its bumps match arthropod <a href="https://abc7chicago.com/post/university-chicago-study-finds-tooth-sensitivity-may-linked-ancient-fish-led-dr-yara-haridy/16499129/" target="_blank" rel="noreferrer noopener">sensilla</a>, not vertebrate dentine.



<h2 class="wp-block-heading" id="h-early-armor-came-with-nerves">Early armor came with nerves</h2>



Sensilla in crabs and scorpions let them taste, feel vibration, and track currents. Early vertebrates adopted a similar strategy, embedding nerves inside mineral caps that hardened into armor.



“Tooth‑like structures likely first evolved in the skin of early vertebrates, prior to the oral invasion of these structures that became teeth,” said <a href="https://biology.ufl.edu/gareth-fraser/" target="_blank" rel="noreferrer noopener">Gareth Fraser</a> of the University of Florida, an evolutionary biologist not involved in the scans.



Because armor muffles most tactile cues, adding built‑in sensors restored environmental awareness without sacrificing defense. The same compromise appears again and again whenever <a href="https://www.earth.com/news/scientists-finally-confirm-species-identity-of-the-dragon-man-fossil-skull-denisovan/">animals</a> grow shells, scales, or plates.



The Ordovician seas teemed with cephalopods and sea scorpions, so feeling a predator brush past could mark the difference between survival and lunch. Even a thin sensory layer offered that edge.



<h2 class="wp-block-heading" id="h-teeth-moved-from-skin-to-mouth">Teeth moved from skin to mouth</h2>



Once fish started lunging at prey, bringing those hard nodules inside the oral cavity made practical sense. The genetic toolkit for building odontodes simply redeployed along the jaw line.



CT reconstructions show a stepwise shift, first lining lips, then clustering on internal ridges that became true teeth. No new tissue was required, only a new address.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/human-teeth-sensitivity_evolution_skate-fish_CT-scan_tooth-like-denticles_Yara-Haridy_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/human-teeth-sensitivity_evolution_skate-fish_CT-scan_tooth-like-denticles_Yara-Haridy_1s.webp" alt="CT scan of the front of a skate, showing the hard, tooth-like denticles (orange) on its skin. Yara Haridy" class="wp-image-1976721"/></a><figcaption class="wp-element-caption">CT scan of the front of a skate, showing the hard, tooth-like denticles (orange) on its skin. Click image to enlarge. Credit: Yara Haridy</figcaption></figure>



This migration explains why modern teeth still flinch when chilled soda hits exposed dentine. The tissue did not lose its ancient job, even after millions of years chewing. 



Human <a href="https://pubmed.ncbi.nlm.nih.gov/21168271/" target="_blank" rel="noreferrer noopener">odontoblast cells</a> inside dentine express <a href="https://www.ncbi.nlm.nih.gov/books/NBK5244/" target="_blank" rel="noreferrer noopener">temperature‑sensing TRP channels</a> that trigger pain signals, reinforcing the link between sensation and tooth structure.



<h2 class="wp-block-heading" id="h-ice-cream-pain-is-ancient">Ice cream pain is ancient</h2>



Skates, sharks, and certain catfish still wear odontodes across their skin, and fluorescent imaging reveals nerves curling around each unit. The same wiring lights up in their oral teeth.



Dentists encounter the legacy daily: about 30 percent of adults report <a href="https://pubmed.ncbi.nlm.nih.gov/34302871/" target="_blank" rel="noreferrer noopener">dentin hypersensitivity</a> - a direct outcome of open tubules harking back to those armored swimmers.



Laboratory studies show that activating <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC4541108/" target="_blank" rel="noreferrer noopener">TRPA1 and TRPV4</a> channels in human odontoblasts releases ATP, a chemical that excites nearby nerves and sparks the familiar zing of ice‑cream pain.



Understanding the fossil record clarifies why blocking tubules with varnishes or bioactive glasses calms sensitivity more reliably than numbing gels alone. Closing the ancient sensory windows cuts the signal at its source.



<h2 class="wp-block-heading" id="h-fossil-mistake-changed-tooth-history">Fossil mistake changed tooth history</h2>



The misidentification of Anatolepis as a vertebrate with dentine pushed the timeline of true teeth further back than the evidence supports. 



With updated scans showing Anatolepis as an arthropod, the emergence of real vertebrate dental tissue now firmly begins in the middle Ordovician.



This correction removes about 40 million years of assumed vertebrate history. It also reorients where scientists search for the evolutionary leap from external skin sensors to internal biting tools.



<h2 class="wp-block-heading" id="h-ancient-teeth-link-to-modern-health">Ancient teeth link to modern health</h2>



Reclassifying Anatolepis as an <a href="https://www.earth.com/news/cambrian-fossils-reveal-new-clues-about-arthropod-evolution/">arthropod</a> pushes the oldest confirmed vertebrate dentine forward by almost 40 million years, tightening the evolutionary timeline. Paleontologists can now focus on <a href="https://www.earth.com/news/470-million-year-old-animal-fossils-discovered-in-frances-cabrieres-biota/">Ordovician</a> strata when hunting the first mouths with teeth.



The fossil findings also challenge textbook diagrams that present teeth as novel structures formed deep inside the jaw. 



Instead, they appear as immigrants from the skin, carrying sensory baggage that still shapes dental health.



Medical researchers already mine shark and skate genes to inspire regenerative dentistry. Knowing those genes once built skin sensors may guide efforts to coax human cells into growing replacement enamel.



Finally, the study highlights a broader pattern: nature often solves different problems with the same parts. 



Sensory armor, lateral‑line canals, and even mammal whiskers show how sensation sneaks into protective structures whenever the need arises.



The study is published in <a href="https://www.nature.com/articles/s41586-025-08944-w" target="_blank" rel="noreferrer noopener">Nature</a>.



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Fossil discovery explains why our teeth are still so sensitive to cold

For most of us, teeth mean crunching pretzels or tearing...

Earth’s earliest complex organisms endured harsh environments, and a new study reveals how these ancient life forms used arsenic to survive.



Researchers studied 2.1-billion-year-old fossils from Gabon’s Francevillian Basin. These fossils belong to eukaryotes, <a href="https://www.earth.com/news/tiny-microbes-may-have-given-rise-to-complex-life/">organisms</a> with advanced cells.



The team found that these ancient organisms stored arsenic inside special cell compartments. This strategy helped them survive in seas with even low arsenic levels.



Using advanced X-ray technology, they mapped arsenic inside of the fossils. The analysis revealed that arsenic was not the result of later contamination. Instead, it was locked inside during the organisms’ lives.



<h2 class="wp-block-heading" id="h-ancient-seas-triggered-arsenic-defenses">Ancient seas triggered arsenic defenses</h2>



The study offers a fresh view of early <a href="https://www.earth.com/news/world-turtle-day-2025-ancient-creatures-with-modern-challenges/">life</a>’s fight against toxins. The fossils lived in oxygen-rich seas with plenty of phosphate. However, even in these waters, arsenate - the toxic form of arsenic - posed a problem.



“The ability to cope with arsenic was not something eukaryotes developed randomly,” explained Dr. Ernest Chi Fru from <a href="https://www.cardiff.ac.uk" target="_blank" rel="noreferrer noopener">Cardiff University</a>.



During this period, Earth’s oxygen levels began to rise. This change made arsenate more common. Since arsenate closely resembles phosphate, it easily entered cells.



Organisms faced a tough challenge. They needed ways to avoid poisoning while still absorbing phosphate, a nutrient essential for life.



<h2 class="wp-block-heading" id="h-fossils-show-arsenic-stored-in-bodies">Fossils show arsenic stored in bodies</h2>



The fossils showed high arsenic concentrations, far above the levels in surrounding rocks. This suggests they absorbed arsenic during their lifetime.



X-ray imaging revealed arsenic at the core of tiny pyrite crystals inside the <a href="https://www.earth.com/news/cambrian-explosion-fossils-push-back-the-rise-of-complex-life/">fossils</a>. This points to a biological origin. The arsenic likely came from within the organisms, not from the environment after burial.



Other structures in the same rocks did not show such patterns. Abiotic concretions nearby lacked this arsenic core structure. Similar arsenic-rich patterns appear in some younger animal fossils. However, they are absent in purely mineral samples.



This difference suggests that the Francevillian organisms actively stored arsenic. It wasn’t simply absorbed from surrounding waters after death.



<h2 class="wp-block-heading" id="h-arsenic-storage-for-survival">Arsenic storage for survival</h2>



The researchers tested three scenarios to explain arsenic in the <a href="https://www.earth.com/news/why-we-see-some-animals-as-more-human-than-others/">fossils</a>. First, they ruled out passive absorption from decaying organic material. 



Second, the team dismissed the idea that sulfate-reducing microbes introduced the arsenic. The most likely explanation was bioaccumulation. These organisms absorbed arsenic during their lifetime and stored it inside their bodies.



“This suggests a pronounced biogenic control on arsenic storage,” wrote the researchers. They argue that arsenic storage was not just a survival trick. It was an adaptation tied to the rise of oxygen in Earth’s oceans.



<h2 class="wp-block-heading" id="h-arsenic-damaged-ancient-life-systems">Arsenic damaged ancient life systems</h2>



Arsenic disrupts life by mimicking phosphate. Once inside cells, it blocks key processes like energy production and genetic functions.



Modern organisms use efflux pumps or special enzymes to remove arsenic. Some even store it safely in vacuoles or vesicles.



The fossils showed traces of arsenic linked with other metals like nickel and copper. These metals can also be toxic in high amounts.



This suggests the organisms had a broader detoxification system. They may have stored multiple harmful elements together.



<h2 class="wp-block-heading" id="h-modern-sponges-use-similar-storage">Modern sponges use similar storage</h2>



The researchers drew comparisons with modern sponges. These ancient animals often store arsenic in special compartments.



Sponges use this strategy because it helps them manage metal exposure from their filter-feeding lifestyle.



The Francevillian organisms might have done something similar. Their environment had low arsenic levels, but long-term exposure likely led to gradual buildup inside their bodies.



The stored arsenic later formed pyrite crystals during fossilization. The researchers’ model shows how this process left clear chemical markers in the fossils.



<h2 class="wp-block-heading" id="h-the-evolution-of-complex-life">The evolution of complex life</h2>



The findings suggest that arsenic detoxification emerged very early in the evolution of eukaryotic life. It was likely not a rare or isolated event. 



Instead, the ability to manage arsenic probably evolved multiple times throughout Earth’s long history, as different organisms adapted to shifting environmental conditions.



These arsenic-rich fossils reveal much more than just details about ancient organisms. They serve as powerful tools for researchers, offering a way to detect signs of early life in rocks that are billions of years old. 



The chemical traces left behind provide strong clues about how life evolved and adapted in hostile environments.



<h2 class="wp-block-heading" id="h-survival-strategies-of-ancient-life">Survival strategies of ancient life</h2>



Ultimately, the research highlights the importance of chemical signatures as records of biological processes. 



Even when organic material disappears, these chemical patterns can tell the story of ancient survival strategies and environmental challenges.



By storing arsenic within their cells, these early organisms developed a unique way to survive in toxic seas. In doing so, they not only overcame dangerous conditions but also preserved a chemical fingerprint that allows scientists today to uncover their ancient existence.



The study is published in the journal <a href="https://www.nature.com/articles/s41467-025-59760-9" target="_blank" rel="noreferrer noopener">Nature Communications</a>.



Image Credit: Arnaud Mazurier and Abderrazak El Albani



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Why ancient organisms stored arsenic inside their cells

Earth’s earliest complex organisms endured harsh environments, and a new...

When researchers lowered a cow carcass 5,345 feet (1,629 meters) beneath the waves off Hainan Island, they were studying natural whale fall processes in the deep sea. Instead, the bait attracted uninvited guests never before filmed in these waters: Pacific sleeper sharks (Somniosus pacificus).



The video, captured on the continental slope of the northern South China Sea, marks the species’ southernmost sighting in the Pacific Basin. 



It also reveals a suite of behaviors - from polite feeding queues to protective eye retractions - that deepen our understanding of how large predators survive in the deep ocean.



<h2 class="wp-block-heading" id="h-sharks-spotted-far-from-home">Sharks spotted far from home</h2>



Until now, Pacific sleeper sharks were considered residents of the North Pacific, with records stretching from Japan and the <a href="https://www.earth.com/news/why-did-billions-of-crabs-vanish-from-the-bering-sea/">Bering Sea</a> to Alaska and as far south as Baja California. Their sudden appearance in tropical latitudes stunned marine biologists.



The deployment, designed to mimic a natural whale fall, quickly drew multiple sharks that took turns tearing at the carcass. 



Because sleeper sharks routinely dive below 3,280 feet (1,000 meters), direct observations have been scarce. Remote baited cameras provided the first clear window into their deep-sea routines.



<h2 class="wp-block-heading" id="h-size-shapes-shark-feeding-style">Size shapes shark feeding style</h2>



Back on shore, the research team reviewed hours of footage and divided the sharks into two categories: individuals longer than 8.85 feet (2.7 meters) and those shorter. 



The threshold was chosen purely as a reference point, not as a marker of maturity.



<a href="https://www.earth.com/news/how-the-sharks-body-grows-with-geometric-precision/">Size</a> proved to be a major factor in feeding style. The bigger sharks charged the carcass head-on, ripping chunks of flesh with sweeping bites. Smaller sharks kept their distance, circling watchfully before making tentative nips. 



The contrast suggests a competitive hierarchy in which bulk confers priority access to limited resources.



<h2 class="wp-block-heading" id="h-sharks-take-polite-turns">Sharks take polite turns</h2>



Perhaps the most unexpected behavior was a kind of underwater etiquette. As each shark finished feeding, it glided away, making room for the next arrival. 



<a href="https://spj.science.org/doi/10.34133/olar.0095" target="_blank" rel="noreferrer noopener">On the video camera footage</a>, the handover looked almost orderly, with newcomers approaching steadily from behind while current feeders yielded position.



“This behavior suggests that feeding priority is determined by individual competitive intensity, even in deep-water environments," said study author Han Tian, a marine biologist at <a href="https://www.sysu.edu.cn/sysuen/">Sun Yat-sen University</a>. 



"This reflects a survival strategy suitable for non-solitary foraging among Pacific sleeper sharks.”



Comparable line-ups have been reported when sharks scavenge floating whale carcasses near the surface, where space is equally contested. 



The deep-sea footage indicates that such social rules persist even in the aphotic zone, where encounters are rare and every calorie counts.



<h2 class="wp-block-heading" id="h-defensive-eye-roll"><a></a>Defensive eye roll</h2>



Pacific sleeper sharks lack the nictitating membrane - a transparent eyelid - found in many shark species. Yet the video shows them repeatedly retracting their eyes while feeding.



Scientists interpret this as a built-in safeguard against sudden jabs from protruding bones or the teeth of rival sharks. 



The involuntary eye roll could compensate for the missing membrane, protecting vision during frenzied meals.



<h2 class="wp-block-heading" id="h-clues-to-an-expanded-range"><a></a>Clues to an expanded range</h2>



Finding Pacific sleeper sharks 1,800 miles (3,000 kilometers) south of their documented range forces scientists to rethink what governs their distribution. 



Do shifting <a href="https://www.earth.com/news/ocean-temperatures-are-rising-faster-than-expected-and-likely-to-accelerate/">ocean temperatures</a> invite them farther into the tropics? Or does the South China Sea offer prey reservoirs that make the journey worthwhile?



All individuals filmed were female - a pattern echoed by other rarely seen giants such as the megamouth shark, which also shows a female bias here. 



The sex skew hints that the region might double as a nursery or feeding ground for pregnant sharks needing high-energy meals.



<h2 class="wp-block-heading" id="h-energy-in-the-abyss">Energy in the abyss</h2>



Large predators cannot thrive without a steady food supply. Sleeper sharks typically scavenge or ambush seals and squids in colder waters.



In the subtropical South China Sea, their presence implies robust nutrient pathways moving organic matter from surface ecosystems to abyssal depths.



<figure class="wp-block-image aligncenter size-full"><a href="https://spj.science.org/doi/10.34133/olar.0095" target="_blank" rel="noreferrer noopener"><img src="https://www.earth.com/wp-content/uploads/2025/07/pacific-sleeper-sharks_rare-observations_deep-ocean_SME-DEEP_1s.webp" alt="The presence of Pacific sleeper sharks of varying body sizes was detected in the deep waters of the South China Sea using stationary cameras, with all individuals identified as female. Credit: Ocean-Land-Atmosphere Research" class="wp-image-1976702"/></a><figcaption class="wp-element-caption">The presence of Pacific sleeper sharks of varying body sizes was detected in the deep waters of the South China Sea using stationary cameras, with all individuals identified as female. Click image to watch the video. Credit: Ocean-Land-Atmosphere Research</figcaption></figure>



“The highly aggressive behavior of sharks observed in the South China Sea suggests that this region still harbors abundant food sources in the deep sea," Tan said. 



"But what exactly are they? This question is intriguing for both animal distribution and behavioral research.”



<h2 class="wp-block-heading" id="h-tracking-sharks-in-the-deep">Tracking sharks in the deep</h2>



The team plans to deploy additional baited cameras and <a href="https://www.earth.com/news/dna-fishing-helps-scientists-survey-marine-life-in-the-deep-ocean/">environmental DNA</a> samplers across the basin to gauge how many Pacific sleeper sharks prowl these depths and whether they stay year-round. 



Comparative studies from other oceans could reveal whether deep-water queuing is widespread among large scavengers or unique to this lineage.



Biologists also hope to determine if <a href="https://www.earth.com/news/danger-zones-climate-change-is-altering-predator-prey-dynamics/">climatic changes</a> or altered current patterns are drawing cold-adapted predators southward. 



Answers will feed into global models of deep-sea energy flow and illuminate how carbon moves from surface waters to the seafloor, a key piece of the climate puzzle.



For now, the footage shatters old assumptions. Pacific sleeper sharks are not confined to polar and subpolar seas. 



They form loose social hierarchies, even in perpetual darkness, and they may rely on uncharted nutrient highways that link surface productivity with the deep ocean.



-----



<a href="https://spj.science.org/doi/10.34133/olar.0095" target="_blank" rel="noreferrer noopener">Click here to watch the full video footage...</a>



The study is published in the journal <a href="https://spj.science.org/doi/10.34133/olar.0095" target="_blank" rel="noreferrer noopener">Ocean-Land-Atmosphere Research</a>.



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Rare video shows elusive deep-sea predators feeding thousands of miles from home

When researchers lowered a cow carcass 5,345 feet (1,629 meters)...

Greenland sharks cruise the North Atlantic at a pace slower than most people walk, yet some were already adults when the United States was founded. 



Their astonishing lifespan has turned this elusive fish into a living time capsule, capturing the imagination of biologists and longevity researchers alike.



Julius Nielsen of the <a href="https://www.ku.dk/en" target="_blank" rel="noreferrer noopener">University of Copenhagen</a> leads many of the modern expeditions that tag, scan, and sometimes briefly corral these giants in the icy dark.



<h2 class="wp-block-heading" id="h-why-greenland-sharks-live-so-long">Why Greenland sharks live so long</h2>



<a href="https://www.science.org/doi/10.1126/science.aaf1703" target="_blank" rel="noreferrer noopener">Eye‑lens radiocarbon dating</a> shows females can live at least 272 years, with one specimen estimated at 392 ± 120 years. The method pinpoints birth dates because the lens proteins stop exchanging carbon after a shark pup forms in utero.



“This is the longest living vertebrate that we know of,” said Nielsen, who helped age the record fish. He and colleagues calculate that females do not reach sexual maturity until roughly 150 years, a timetable unheard of in other sharks.



Slow annual growth, barely half an inch, means injuries heal gradually but bones and organs escape the cumulative cellular wear seen in faster‑growing <a href="https://www.earth.com/news/shark-skeletons-could-lead-to-technological-innovations/">animals</a>. 



Researchers suspect a combination of frigid water, low oxygen demand, and genes that police DNA damage all contribute, yet no single “silver bullet” for longevity has appeared.



<h2 class="wp-block-heading" id="h-greenland-sharks-have-slow-heartbeats">Greenland sharks have slow heartbeats</h2>



Greenland sharks have resting <a href="https://journals.biologists.com/jeb/article/221/19/jeb186957/33812" target="_blank" rel="noreferrer noopener">heart rates</a> of about 10 beats per minute and unusually low blood pressure. That’s much lower than what you’d find in other large sharks, and it may help protect their blood vessels from long-term damage like heart attacks or strokes.



Even with such a slow heartbeat, each pump moves a lot of blood, keeping their <a href="https://www.earth.com/news/different-shark-species-seen-scavenge-feeding-together-in-rare-event/">bodies</a> fueled during slow swimming under Arctic ice. 



Doctors are paying attention, hoping this natural “strong pump, gentle pressure” system could offer ideas for treating high blood pressure in people.



<h2 class="wp-block-heading" id="h-slow-bodies-save-energy">Slow bodies save energy</h2>



These sharks burn energy very slowly. In fact, their oxygen use is among the <a href="https://www.nature.com/articles/s41598-020-76371-0" target="_blank" rel="noreferrer noopener">lowest ever recorded</a> for a fish their size. That kind of slow metabolism may reduce cell damage over time and help them survive long gaps between meals. 



A 280-pound shark might get through the day on fewer calories than a cheeseburger, making a single big meal last for months.



Because the deep Arctic is so cold, they digest food slowly too. Instead of burning energy for speed or growth, they stretch it out for <a href="https://www.earth.com/news/mediterranean-sharks-face-growing-threats-despite-conservation-efforts/">survival</a>.



<h2 class="wp-block-heading" id="h-why-they-are-toxic-top-predators">Why they are toxic top predators</h2>



Greenland shark meat is laced with <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC5127123/" target="_blank" rel="noreferrer noopener">trimethylamine N‑oxide</a>, a compound that stabilizes proteins under high pressure yet renders the raw flesh neurotoxic to mammals.



Icelanders neutralize it through months of fermentation to create the ceremonial dish kæstur hákarl, but few tourists finish more than a nibble.



The species ranks as an apex predator; evidence shows adults seizing fish, squid, and the occasional sleeping seal. 



Sightings in the Gulf of Mexico and off Spain reveal a wider range than once believed, hinting at deep‑water corridors that connect polar and temperate seas.



<h2 class="wp-block-heading" id="h-greenland-sharks-are-at-risk">Greenland sharks are at risk</h2>



Commercial trawlers unintentionally haul up about 3,500 Greenland <a href="https://www.forbes.com/sites/melissacristinamarquez/2022/11/07/greenland-shark-finally-gets-protection/" target="_blank" rel="noreferrer noopener">sharks</a> each year as bycatch. Because breeding may not begin for a century and a half, losing even sub‑adults chips away at population recovery.



The <a href="https://www.iucnredlist.org/species/60213/3112909" target="_blank" rel="noreferrer noopener">International Union for Conservation of Nature</a> lists the species as “Vulnerable,” citing low fecundity and expanding deep‑sea fisheries. 



Simple changes, switching to LED‑lit nets that deter sharks, banning deep set gill nets in nursery zones, and funding release‑training for crews, can cut mortality without shrinking catches of cod or halibut.



Scientists also urge Arctic nations to establish no‑take refuges around known mating aggregations once those secret sites are found. Protecting a fish that may still be swimming in 2425 demands policies that look far beyond typical political horizons.



<h2 class="wp-block-heading" id="h-the-search-for-hidden-nursery-grounds">The search for hidden nursery grounds</h2>



No one has ever observed Greenland sharks mating or giving birth in the wild. Only one pregnant female has been studied, and her embryos suggest the species may be <a href="https://www.fisheries.noaa.gov/feature-story/sharpen-your-shark-facts" target="_blank" rel="noreferrer noopener">aplacental viviparous</a>, meaning the young develop inside eggs that hatch within the mother’s body.



Females seem to carry up to 10 pups at a time, but the <a href="https://www.fisheries.noaa.gov/feature-story/five-wild-facts-about-shark-reproduction" target="_blank" rel="noreferrer noopener">gestation period</a> could last several years. Without regular breeding or nursery sightings, it's hard to estimate how often they reproduce or whether their range shifts during these vulnerable periods.



This gap in knowledge makes population modeling difficult. Without better data, scientists can't say how quickly these sharks could recover if current bycatch trends continue. 



Tagging mature females may help reveal mating routes or hidden nursery grounds. Learning how and where they reproduce could play a key role in designing effective marine protected areas.



The study is published in the journal <a href="https://www.science.org/doi/10.1126/science.aaf1703" target="_blank" rel="noreferrer noopener">Science</a>.



Image Credit: Julius Nielsen



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Longest-living vertebrates on Earth survive for centuries in icy waters

Greenland sharks cruise the North Atlantic at a pace slower...

Bumble bees, like humans, sometimes eat the wrong things. A new study shows they may pick foods that don’t meet their nutritional needs - and those choices might actually harm their health.



In research conducted at <a href="https://www.psu.edu/">Penn State University</a>, scientists found that when bumble bees were offered diets enriched with varying levels of protein, fat, and carbohydrates, their eating habits didn’t lead to better health. 



The study raises new questions about how bees choose what to eat - and whether those choices are good for them.



<h2 class="wp-block-heading" id="h-bumble-bees-don-t-choose-healthy-options">Bumble bees don't choose healthy options</h2>



The researchers designed a controlled study where bumble bees were split into groups and given specific diets. Some groups received <a href="https://www.earth.com/news/bee-survival-depends-on-more-than-just-pollen-abundance/">pollen</a> with added protein or fat. Others got nectar-like sugar solutions with different sugar levels. 



A control group was allowed to eat a standard diet of wild pollen and a 60% sugar solution. All the bees were the same age and housed in small groups to keep testing conditions consistent. 



What happened next surprised the researchers. The bumble bees didn't go for the food options that were healthy. 



The bees ate more when protein levels in pollen were higher, less when fat levels were higher, and they over-consumed sugar when the nectar was watered down. 



None of the eating patterns benefited the physical health of the bumble bees. Egg-laying declined. Body weight stayed the same or dropped. Nothing the bees chose to eat led to better outcomes than the control group.



<h2 class="wp-block-heading" id="h-bumble-bees-make-bad-food-choices">Bumble bees make bad food choices</h2>



The results challenge the long-standing assumption that bees instinctively know what to eat to stay healthy.



Etya Amsalem is an associate professor of entomology in the College of Agricultural Sciences and lead author of the study. She noted that bee preferences are unlikely to reflect true needs and more likely result from evolutionary constraints.



“For instance, bees may under-consume lipids not because high-lipid diets are harmful, but because their physiology is not well-suited for digesting or storing large amounts of lipids," said Professor Amsalem.



“Bees may over-consume proteins because they have evolved to seek them out whenever they’re available, even though excess protein can be detrimental because it affects how efficiently bees can eliminate nitrogen from their bodies."



This mismatch - between what bees eat and what actually helps them - may be putting more strain on already vulnerable bee populations.



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



Bumble bees are under serious stress worldwide. Habitat loss, <a href="https://www.earth.com/news/pesticides-attack-bees-in-multiple-ways-throughout-the-body/">pesticide</a> exposure, climate change, and industrial farming have drastically reduced the variety and quality of flowers bees depend on. 



In many areas, rich, diverse meadows have been replaced by monocultures or urban development. That leaves bees with fewer options - and often with subpar food sources.



This drop in floral diversity doesn’t just mean less food overall - it means less nutritionally balanced food. Even when bees find enough to eat, the quality of that food may not support key functions like reproduction, colony growth, or immune strength.



Nutrition plays a big role in <a href="https://www.earth.com/news/organic-farming-and-flower-strips-improve-honey-bee-health/">bee health</a>. But if bees can’t always tell what’s good for them, that complicates conservation efforts.



“It’s an odd assumption when you think about it - my toddler prefers chocolate over broccoli, but I wouldn’t conclude from that that chocolate is healthier for her,” said Professor Amsalem. 



“So, why do we assume bees are different? Understanding potential mismatches between consumption and fitness outcomes is important, as most conservation and management strategies assume bees can self-regulate their diets for optimal health.”



<h2 class="wp-block-heading" id="h-rethinking-bumble-bee-health">Rethinking bumble bee health</h2>



The results suggest that preference alone isn’t a reliable guide for diet planning - not for bees, and likely not for conservation strategies either. 



Instead of assuming bees will naturally eat what’s best for them, the researchers say we need a deeper understanding of how diet affects their health at a physiological level. According to Professor Amsalem, future research needs to dig deeper.



“Future research could investigate why bees fail to optimize diet - for example, metabolic limitations, gustatory biases or ecological tradeoffs - and may explore nonmacronutrient components like vitamins and minerals that may explain fitness discrepancies,” she said.



For conservation groups, farmers, and scientists trying to support healthy bee populations, this study is a clear reminder: what bees choose to eat may not be what’s best for them. And that makes understanding their real nutritional needs more urgent than ever.



The full study was published in the journal <a href="https://linkinghub.elsevier.com/retrieve/pii/S0022191025000769">Journal of Insect Physiology</a>.



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How bumble bees are sabotaging their own health

Bumble bees, like humans, sometimes eat the wrong things. A...

Off the eastern tip of Java, dredging barges dragged up more than sand. They pulled a piece of the past: a submerged river valley under the Madura Strait packed with fossils that had slept under fifty feet of water since long before the last Ice Age melted away.



Among the finds were two skull fragments of Homo erectus, a <a href="https://www.earth.com/news/fossil-discovery-anadoluvius-turkae-suggests-humans-originated-in-europe-not-africa/">human ancestor</a> that roamed Asia until roughly 117,000 years ago, as well as more than 6,000 animal fossils that paint a vivid portrait of a lost ecosystem. <a href="https://www.universiteitleiden.nl/en/staffmembers/harry-berghuis" target="_blank" rel="noreferrer noopener">Harold Berghuis</a> of <a href="https://www.universiteitleiden.nl/en" target="_blank" rel="noreferrer noopener">Leiden University</a> leads the team studying the haul.



<h2 class="wp-block-heading" id="h-sundaland-rises-then-sinks">Sundaland rises then sinks</h2>



During colder glacial times, much of Southeast Asia’s continental shelf formed a single low‑lying continent known as <a href="https://www.cepf.net/our-work/biodiversity-hotspots/sundaland#:~:text=The%20Sundaland%20Biodiversity%20Hotspot%20covers,islands%20of%20Borneo%20and%20Sumatra." target="_blank" rel="noreferrer noopener">Sundaland</a>. 



Sea level then sat about 400 feet lower than it does today, exposing wide plains crisscrossed by rivers and grasslands.



When global ice melted between <a href="https://www.nature.com/articles/s42003-023-04510-0" target="_blank" rel="noreferrer noopener">22,000 and 6,000 years ago</a>, the ocean climbed roughly 443 feet, drowning half of that landmass. 



The rapid pulses of rise carved islands out of peninsulas and pushed coastlines hundreds of miles inland, isolating plants, animals, and the people who depended on them.



Geologists can still follow the drowned river channels with high‑resolution sonar. Each channel marks a corridor that once connected Borneo, Sumatra, and Java to the Asian mainland, providing migration routes for both megafauna and hominins.



<h2 class="wp-block-heading" id="h-river-fossils-under-the-madura-strait">River fossils under the Madura Strait</h2>



The valley now mapped under the Madura Strait was carved by the ancient Solo River. 



Optically Stimulated Luminescence dating (<a href="https://www.antarcticglaciers.org/glacial-geology/dating-glacial-sediments-2/optically-stimulated-luminescence/" target="_blank" rel="noreferrer noopener">OSL</a>) shows its sandy fill settled between 162,000 and 119,000 years ago, anchoring the new fossils to the late <a href="https://www.sciencedirect.com/science/article/pii/S295023652500012X" target="_blank" rel="noreferrer noopener">Pleistocene</a>.



OSL works because quartz grains store energy from cosmic rays like tiny batteries. When technicians shine a laser on a grain in the lab, it releases that stored charge as light, revealing the moment the grain last basked in sunlight.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/madura-strait_sunda-shelf_homo-erectus-remains_map_credit-ScienceDirect_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/madura-strait_sunda-shelf_homo-erectus-remains_map_credit-ScienceDirect_1s.webp" alt="The Sunda Shelf of Southeast Asia, with the Indonesian archipelago. Box indicates the position of map B. B: Eastern Java, the Madura Strait, the Solo River, Ngandong, Sambungmacan, and other hominin sites. Box indicates the position of map C. C: The Madura Strait north of Surabaya, with the sand extraction area and the location of the BMS land-reclamation. Map data: GEBCO and ALOS" class="wp-image-1976530"/></a><figcaption class="wp-element-caption">The Sunda Shelf of Southeast Asia, with the Indonesian archipelago. Box indicates the position of map B. B: Eastern Java, the Madura Strait fossils location, the Solo River, Ngandong, Sambungmacan, and other hominin sites. Box indicates the position of map C. C: The Madura Strait north of Surabaya, with the sand extraction area and the location of the BMS land-reclamation. Click image to enlarge. Map data: GEBCO and ALOS</figcaption></figure>



The method is ideal for underwater sites where radiocarbon fails, yet it is rarely applied because retrieving uncontaminated samples from the seafloor is difficult. 



The Madura team’s success shows how pipeline spoil, often discarded as waste, can become forensic evidence on continental‑scale change.



<h2 class="wp-block-heading" id="h-madura-strait-reveals-fossil-menagerie">Madura Strait reveals fossil menagerie</h2>



The tally of species rivals a natural‑history museum catalog. There were buffalo, several kinds of deer, and <a href="https://nationalzoo.si.edu/animals/komodo-dragon" target="_blank" rel="noreferrer noopener">Komodo dragons</a> longer than a canoe.



The biggest draw, though, is <a href="https://eartharchives.org/articles/stegodon-the-elephant-with-sideways-trunk/index.html" target="_blank" rel="noreferrer noopener">Stegodon trigonocephalus</a>, an elephant‑like giant that could stand almost 13 feet at the shoulder. 



Its presence suggests tall grass and open water holes, conditions that match pollen studies from upland Java.



Fossil monitors link today’s dragon‑patrolled islands to their mainland roots; remains of <a href="https://ielc.libguides.com/sdzg/factsheets/komododragon" target="_blank" rel="noreferrer noopener">Varanus komodoensis</a> have turned up on nearby <a href="https://www.theextinctions.com/articles-1/lesser-sunda-islands-part-1-flores-and-sumba" target="_blank" rel="noreferrer noopener">Flores and Sumba</a>, confirming that the apex lizard once ranged far beyond its present refuges. 



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/maduro-strait_indonesia_homo-erectus_ancient-remains_credit-ScienceDirect_1m.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/maduro-strait_indonesia_homo-erectus_ancient-remains_credit-ScienceDirect_1s.webp" alt="Madura Strait 1 (MS1): Homo erectus frontal fragment with dextral supraorbital torus. A: Photographs. B: CT-based 3D surface rendered images. Note that the exact orientation of the fragment is unknown. For the anterior view, a slightly diagonal orientation has been assumed. C: CT-based 3D surface rendered image of MS1 in a more horizontal orientation, with anatomical indications. D: CT-slice. Credit: ScienceDirect" class="wp-image-1976532"/></a><figcaption class="wp-element-caption">Madura Strait 1 (MS1) fossils: Homo erectus frontal fragment with dextral supraorbital torus. A: Photographs. B: CT-based 3D surface rendered images. Note that the exact orientation of the fragment is unknown. For the anterior view, a slightly diagonal orientation has been assumed. C: CT-based 3D surface rendered image of MS1 in a more horizontal orientation, with anatomical indications. D: CT-slice. Click image to enlarge. Credit: ScienceDirect</figcaption></figure>



Carnivore teeth in the assemblage are scarce, hinting that reptiles, not big cats, topped the food chain.



Antelope‑like bovids and open‑country rodents round out the scene, pointing to savanna rather than rainforest. Together the bones sketch a community more East African than Indonesian.



<h2 class="wp-block-heading" id="h-humans-with-tools-and-strategy">Humans with tools and strategy</h2>



Researchers counted more than 300 bones marked by stone blades or flakes. Some show percussion scars where marrow was pounded out.



“The Sunda Shelf played an important role in the dispersal and evolution of hominin populations,” wrote Berghuis and colleagues in their 2025 report. Others bear parallel slices typical of tendon removal.&nbsp;



“Thus far, hominin <a href="https://www.earth.com/news/archaeopteryx-fossil-soft-tissue-flight-evolution-proves-darwin-right/">fossils</a> from submerged Sundaland were not available.” The Madura Strait fragments break that drought. Underscoring the novelty of the find.&nbsp;



Tool cut geometry matches <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC4920301/" target="_blank" rel="noreferrer noopener">Acheulean‑derived technologies</a> already known from Java’s terrestrial sites. That continuity supports the idea that people followed rivers seasonally, carrying simple gear that was easy to replace when tools were lost in mud or water.



<h2 class="wp-block-heading" id="h-what-the-skulls-add-to-the-story">What the skulls add to the story</h2>



Although each piece is only a few inches across, the brow ridge profile and bone thickness match late <a href="https://pubmed.ncbi.nlm.nih.gov/18479734/" target="_blank" rel="noreferrer noopener">Homo erectus skulls</a> dug from Ngandong and Sambungmacan farther up the Solo. 



That link pushes the species’ confirmed range hundreds of miles east, showing it followed river corridors onto the shelf when sea level was low.



One fragment comes from an adolescent, the other from a lightly built adult. Their presence alongside butchered game hints that family groups, not lone hunters, roamed the valley.



<figure class="wp-block-image aligncenter size-full"><a href="https://www.earth.com/wp-content/uploads/2025/07/maduro-strait_indonesia_homo-erectus_skull_credit-ScienceDirect_1.jpg"><img src="https://www.earth.com/wp-content/uploads/2025/07/maduro-strait_indonesia_homo-erectus_skull_credit-ScienceDirect_1s.webp" alt="3D surface images of MS1 and Sambungmacan 3 (anterior view). This comparative skull has the closest metric and morphological match with MS1. Credit: ScienceDirect" class="wp-image-1976534"/></a><figcaption class="wp-element-caption">3D surface images of Madura Strait (MS1) and Sambungmacan 3 (anterior view) fossils. This comparative skull has the closest metric and morphological match with MS1. Click image to enlarge. Credit: ScienceDirect</figcaption></figure>



Because no fire traces were found, the visitors probably camped on higher terraces that are now long submerged. 



The bones they left behind washed into lower channels during seasonal floods and were sealed beneath overbank sand.



<h2 class="wp-block-heading" id="h-looking-for-cousins-beneath-the-waves">Looking for cousins beneath the waves</h2>



The Solo River was only one of many channels draining Sundaland. As survey vessels map more buried valleys, archaeologists expect to meet a wider cast: <a href="https://www.earth.com/news/mysterious-denisovan-species-humans-lived-undisturbed-tibetan-plateau-160000-years/">Denisovans</a>, perhaps, or even the diminutive <a href="https://australian.museum/learn/science/human-evolution/homo-floresiensis/" target="_blank" rel="noreferrer noopener">Homo floresiensis</a>.



Every bucket of dredged sand now promises not just minerals for construction but clues to human origins. 



Underwater archaeology once focused on shipwrecks; now it is turning to paleolandscapes that could double the search area for early humans in Southeast Asia.



The Indonesian government is drafting guidelines that will require sand‑mining companies to report <a href="https://www.earth.com/news/scientists-find-a-47-million-year-old-cicada-fossil-with-preserved-wing-details/">fossil</a> finds within 48 hours. 



Those rules could transform commercial dredges into accidental research partners, expanding the data set at a fraction of normal field costs.



For now the Madura Strait cache stands alone, yet it already stretches the timeline of underwater archaeology in Asia. 



Skulls, riverbeds, and giant beast bones, all locked together in a drowned landscape, remind us that today’s ocean floor was yesterday’s hunting ground.



The study is published in <a href="https://www.sciencedirect.com/science/article/pii/S295023652500012X?via%3Dihub" target="_blank" rel="noreferrer noopener">Quaternary Environments and Humans</a>.



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Archaeologists find 140,000-year-old human and animal remains at the bottom of the ocean

Off the eastern tip of Java, dredging barges dragged up...

The sea spider, those spindly marine oddities that seem composed almost entirely of legs and claws, just given up their genetic secrets.



An international effort led by the <a href="https://www.univie.ac.at/en/">University of Vienna</a> and the <a href="https://www.wisc.edu/">University of Wisconsin–Madison</a> has delivered the first chromosome-level genome for Pycnogonum litorale, a species common in North Atlantic tide pools.



Stretching across 57 pseudo-chromosomes and paired with extensive developmental transcriptomes, the assembly offers an unprecedented look at how an arthropod can evolve such an extreme body plan. This includes a nearly vanishing abdomen and internal organs that spill far into its limbs.



<h2 class="wp-block-heading" id="h-mapping-the-sea-spider-genome">Mapping the sea spider genome</h2>



To achieve a genome this contiguous, the team combined long-read sequencing with Hi-C proximity data. Long reads captured tens of thousands of DNA bases at a stretch. This helped bridge the repetitive regions that routinely break short-read assemblies.



Hi-C, which measures how DNA folds inside the nucleus, then provided a “scaffolding” map that placed those long contigs into chromosomal order.



“The genomes of many non-canonical laboratory organisms are challenging to assemble, and Pycnogonum is no exception," said first author Nikolaos Papadopoulos, a zoologist at the University of Vienna. 



"Only the combination of modern high-throughput data sources made a high-quality genome possible. This can now serve as a stepping stone for further research.”



Because <a href="https://www.earth.com/news/surprising-breeding-behaviors-of-giant-sea-spiders-revealed/">sea spiders</a> are not standard lab animals, researchers collected specimens by hand, often prying them from kelp during low tide. They then rushed them back to the lab for nucleic acid extraction.



The payoff is a reference genome that joins spider, <a href="https://www.earth.com/news/fossil-reveals-the-first-ancestors-of-scorpions-and-spiders/">scorpion</a>, mite, and horseshoe crab assemblies on public databases. Yet it lacks the duplications that mark other arachnid genomes, making it a vital baseline for evolutionary comparisons.



<h2 class="wp-block-heading" id="h-vanished-gene-vanished-abdomen">Vanished gene, vanished abdomen</h2>



The analysis focused on Hox genes, key developmental regulators shared by animals from fruit flies to humans. One gene turned up missing: abdominal-A (abd-A).



In most arthropods, abd-A helps establish the rear-body segments that carry guts and reproductive organs. Sea spiders, with their virtually absent abdomens, appear to have dispensed with both the physical structure and its genetic architect.



“In arthropods, Hox genes play a central role in the correct specification of the different body segments, explained co-author Andreas Wanninger, who co-led the Vienna team. "In many other animal groups they are essential ‘master controllers’ during body plan development.” 



The disappearance of abd-A mirrors patterns seen in <a href="https://www.earth.com/news/how-mites-survived-without-sex-for-millions-of-years/">mites</a> and barnacles, two other arthropod groups that have independently shrunk or lost their hind segments.



<h2 class="wp-block-heading" id="h-sea-spiders-skipped-genome-doubling">Sea spiders skipped genome doubling</h2>



Spiders and scorpions carry extra copies of almost every gene, relics of an ancient whole-genome duplication that likely fueled innovations such as silk glands and complex venom cocktails.



P. litorale shows no sign of that event. Because sea spiders sit at the very base of the chelicerate lineage, the simplest explanation is that the duplication occurred later. It likely arose within the spider-scorpion branch, rather than in the common ancestor of all chelicerates.



That finding reshapes timelines for when gene families expanded and may help researchers pinpoint which duplications underlie spider-specific traits.



<h2 class="wp-block-heading" id="h-tools-for-growth-and-repair">Tools for growth and repair</h2>



Beyond raw sequence, the consortium generated RNA profiles from embryos and juveniles, capturing when each gene flicks on and off as new body segments form.



Those developmental datasets make the sea spider a promising model for studies of ancestral arthropod development, limb regeneration, and physiological resilience in cold, nutrient-poor seas.



Georg Brenneis, an expert in arthropod development at the University of Vienna, is a senior author of the study.



“From an evolutionary developmental perspective, sea spiders are very interesting: their mode of development may be ancestral for arthropods, but at the same time they boast multiple body plan innovations unique to themselves. Beyond this, they also possess remarkable regenerative abilities.” 



“Now that we have the genome and comprehensive datasets on gene activities during development, we can systematically study all of these aspects on the molecular level,” he said.



<h2 class="wp-block-heading" id="h-editing-limbs-and-trunk">Editing limbs and trunk</h2>



With <a href="https://www.earth.com/news/crispr-used-to-remove-extra-chromosomes-in-down-syndrome-and-restore-cell-function/">CRISPR</a> editing becoming feasible in marine invertebrates, investigators can now ask how the remaining sea spider Hox genes choreograph eight elongated walking legs and a tubular trunk. They can also explore how the animals quickly regrow lost appendages.



Comparative physiologists might search the genome for stress-response genes that let sea spiders thrive in icy fjords, while ecological genomics teams could examine how gene flow operates across their wide geographic ranges.



<h2 class="wp-block-heading" id="h-tracing-ancient-sea-spider-cousins">Tracing ancient sea spider cousins</h2>



Without the duplication, shared sea spider genes likely existed as single copies in the last common chelicerate ancestor.



Aligning those sequences will clarify where new venom toxins arose, when silk machinery evolved, and how immune genes diversified.



The genome also lets scientists investigate regulatory DNA - enhancers, promoters, and non-coding RNAs. These elements rewired a conventional arthropod blueprint into the minimalist sea spider form.



<h2 class="wp-block-heading" id="h-expanding-the-genomic-catalog">Expanding the genomic catalog</h2>



The authors envision expanding the catalog to additional sea spider species to test whether abd-A loss is universal. They also aim to map gains and losses of other developmental genes across the group’s 1,300 known species.



Such work could uncover genetic shortcuts to extreme morphological change - insights that extend far beyond any single marine arthropod.



For now, the P. litorale genome stands as a milestone: the first high-quality reference for the world’s most enigmatic chelicerates. It’s also a reminder that even life’s strangest branches follow molecular rules that genomics can finally reveal.



The study is published in the journal <a href="https://bmcbiol.biomedcentral.com/articles/10.1186/s12915-025-02276-x">BMC Biology</a>.



Image Credit: Richard Lord/ <a href="https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode.en">CC BY-NC-SA 4.0</a>



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All legs, no guts: Sea spider genome stuns scientists

The sea spider, those spindly marine oddities that seem composed...

High in northern Peru, three frogs no bigger than a thumbprint have stepped out of anonymity and into the scientific spotlight. Their world is a maze of wet cliffs, dripping bromeliads, and wind‑scoured ridges where moss carpets the rocks.



“They’re <a href="https://www.earth.com/news/world-frog-day-2025-protecting-natures-tiny-guardians/">small</a> and unassuming, but these frogs are powerful reminders of how much we still don’t know about the Andes,” said Germán Chávez of the Center for Ornithology and Biodiversity (<a href="https://corbidi.org/">CORBIDI</a>). 



Chávez and his colleagues trekked those ridges between 2021 and 2024, often in freezing rain, to reach calling sites above 9,000 feet.&nbsp;



<h2 class="wp-block-heading" id="h-mountains-support-unique-frog-species">Mountains support unique frog species</h2>



The <a href="https://blog.pensoft.net/2025/06/27/hidden-gems-in-the-mist-three-new-frog-species-uncovered-in-northern-peru/cordillera-de-huancabamba-1/" target="_blank" rel="noreferrer noopener">Cordillera de Huancabamba</a> forms a natural break in the Andes, splitting watersheds and isolating species. 



Ecologists classify the region as a <a href="https://www.cepf.net/sites/default/files/tropicalandes_techsummary.pdf" target="_blank" rel="noreferrer noopener">biodiversity hotspot</a>, one of only thirty‑five on Earth where extraordinary endemism collides with severe habitat loss.



"The Cordillera de Huancabamba is not just a remote range - it's a living archive of biodiversity and cultural legacy," said Wilmar Aznaran. "And we've barely scratched the surface."



Isolation breeds novelty, and novelty fills the genus Pristimantis. With 619 described species, Pristimantis is now the most diverse <a href="https://www.earth.com/news/whistling-forest-frogs-recently-discovered-may-be-wiped-out-before-we-learn-about-them/">amphibian</a> genus on the planet.



The new frogs, Pristimantis chinguelas, P. nunezcortezi, and P. yonke, occupy different niches along the same ridge. One clings to cliff faces, one prowls leaf litter beside clear streams, and the smallest tucks itself deep inside tank bromeliads.



<h2 class="wp-block-heading" id="h-confirming-the-new-species">Confirming the new species</h2>



Night surveys began after dusk, when temperatures hovered near 50 °F and fog erased headlamp beams. Team members listened for faint “peep” notes that barely rose above dripping leaves. 



Finding a caller did not end the chase. Each frog had to be photographed, swabbed for DNA, measured, and released without harming delicate skin.



Back in Lima, the researchers compared mitochondrial 16S sequences. Genetic distances exceeded the three‑percent threshold herpetologists often use to flag separate <a href="https://www.earth.com/news/missing-frog-species-alsodes-vittatus-resurfaces-after-130-years/">species</a>, clinching the case for formal description.



<h2 class="wp-block-heading" id="h-many-amphibians-are-poorly-studied">Many amphibians are poorly studied </h2>



All three newcomers enter the IUCN books as <a href="https://www.thebhs.org/publications/the-herpetological-bulletin/issue-number-169-autumn-2024/4079-03-how-many-data-deficient-amphibians-are-threatened-iucn-red-list-assessments-for-amphibian-species-previously-classed-as-data-deficient" target="_blank" rel="noreferrer noopener">Data Deficient</a>, meaning scientists lack enough information to judge extinction risk. 



The label sounds neutral, yet recent reassessments show that roughly half of amphibians that start as Data Deficient later prove threatened.



Formal names unlock funding and legal tools that nameless creatures rarely receive. Conservation plans, environmental‑impact statements, and protected‑area budgets almost always hinge on a taxon’s standing in recognized databases.



<h2 class="wp-block-heading" id="h-indicators-of-climate-shifts">Indicators of climate shifts</h2>



The Cordillera de Huancabamba isn't just a biological goldmine, it’s wrapped in layers of folklore. In nearby villages, frogs are often seen as signs of rain or omens tied to agriculture and spiritual beliefs.



This cultural lens makes local communities key allies for conservation. When researchers name <a href="https://www.earth.com/news/frogs-lead-the-way-in-developing-new-antibiotics/">species</a> after regional icons or traditions, like P. yonke, they honor local identity and encourage stewardship.



Unlike most frogs, species in the <a href="https://www.inaturalist.org/taxa/64811-Pristimantis" target="_blank" rel="noreferrer noopener">Pristimantis genus</a> bypass the tadpole stage entirely. They hatch from eggs as fully formed froglets, ready to climb, hop, and call without ever entering water.



This reproductive shortcut allows them to thrive in places where standing water is rare or seasonal. It also makes them sensitive indicators of climate shifts and microhabitat changes in mountain ecosystems.



<h2 class="wp-block-heading" id="h-frog-species-in-fire-prone-habitats">Frog species in fire-prone habitats</h2>



Each frog occupies an area smaller than four square miles, hemmed in by crop fields and fire scars. Peru recorded about 10,400 wildfires in 2024, more than double its previous record, burning grasslands and cloud‑forest edges alike.



P. chinguelas calls from a road‑cut cliff where charred bamboo still smells of smoke. P. nunezcortezi shares a single stream corridor that now borders new potato plots.



P. yonke lives higher, inside bromeliads at roughly 9,800 feet, in what locals call the <a href="https://lacgeo.com/northern-andean-paramo" target="_blank" rel="noreferrer noopener">páramo</a>, a chilly grassland‑wetland mosaic perched above the treeline. 



Páramo vegetation stores water like a sponge, so every lost bromeliad weakens both the frogs and the human communities farther down‑slope.



“Exploring this area is more than fieldwork - it’s an immersion into wilderness, culture, and resilience,” said Karen Victoriano‑Cigüeñas.&nbsp;



"Many of these mountain&nbsp;ridges&nbsp;are isolated, with no roads and extreme terrain," noted Ivan Wong. "The weather shifts within minutes, and the steep cliffs make every step a challenge. It's no wonder so few scientists have worked here before. But that's exactly why there's still so much to find."



<h2 class="wp-block-heading" id="h-protecting-the-new-frog-species">Protecting the new frog species </h2>



No one has recorded the breeding calls of P. nunezcortezi or P. yonke, so females remain unverified. Diet, predators, and lifespan also remain mysteries for all three species.



Future expeditions will test whether the frogs persist on neighboring ridges or whether each ridge hosts its own micro‑endemic. 



Acoustic monitors and <a href="https://royalsocietypublishing.org/doi/10.1098/rspb.2019.2353" target="_blank" rel="noreferrer noopener">eDNA traps</a> could reveal silent populations hiding in moss tunnels or bromeliad tanks beyond the reach of hikers.



For now, the frogs depend on local goodwill. Community fire patrols, low‑impact grazing, and small protected micro‑reserves can buy time while researchers gather the missing data.



The study is published in the journal <a href="https://evolsyst.pensoft.net/article/148522/" target="_blank" rel="noreferrer noopener">Evolutionary Systematics</a>.



Image Credit: Germán Chávez et. al



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Three new frog species found in Peru face an uncertain future

High in northern Peru, three frogs no bigger than a...

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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

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

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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Ant genes show how evolution created perfect teamwork

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

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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

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

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

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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

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

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



 n

How Norwegian lemmings rapidly evolved into a new species

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

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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Microscopic hairs drive courage in hermit crabs

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

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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

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

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



Image Credit: Charlotte Watteyn



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Climate change is separating wild vanilla from its pollinators

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

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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

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

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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Reef survival may depend on how far baby corals travel

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

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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Therapy horses are helping children heal from trauma

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

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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Why predators attack adult moths instead of caterpillars

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

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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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Female dominance in primates is more common than we thought

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

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



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



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



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



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



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



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



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



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



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



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



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



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



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



“Chlorothalonil is particularly common in orchards and vineyards, and is often used preventatively when no disease is present,” explained Professor Ponton. 



“People assume <a href="https://www.earth.com/news/wild-birds-are-significantly-threatened-by-vineyard-fungicides/">fungicides</a> like chlorothalonil only impact fungal diseases, but they can have devastating, unintended consequences for other species,” she stated.



<h2 class="wp-block-heading" id="h-fungicide-fuels-insect-decline">Fungicide fuels insect decline </h2>



The study revealed that chlorothalonil exposure during the larval stage caused major reproductive issues in the adult flies.



Female flies were smaller, had fewer egg-producing structures, and laid far fewer eggs. Male flies had lower iron levels, which can interfere with sperm production and other metabolic functions.



The researchers also checked whether the flies were avoiding the contaminated food. They weren’t.



“We didn’t find a significant aversion for food contaminated with chlorothalonil, except when there was a very high concentration of the chemical,” explained Professor Ponton. “This means the impacts are due to chlorothalonil ingestion.”



<h2 class="wp-block-heading" id="h-effects-on-insect-pollinators">Effects on insect pollinators</h2>



In agricultural settings where whole crops are treated with fungicides, insects like flies and bees have no way to avoid the chemicals. This creates a larger problem for <a href="https://www.earth.com/news/parasitic-plant-has-some-unlikely-allies-for-pollination-and-seed-dispersal/">pollination</a>, ecosystem stability, and food production.



“We need <a href="https://www.earth.com/news/some-bees-value-quality-over-quantity-in-flower-selection/">bees</a> and flies and other beneficial insects for pollination, and we think this is an important problem for pollinator populations,” said Professor Ponton. “There is a strong commercial incentive to understand the impact in the field and address the use of this chemical.”



Despite the widespread use of <a href="https://www.publiceye.ch/en/topics/pesticides/chlorothalonil-a-banned-pesticide-exported-from-europe">chlorothalonil</a>, there's a surprising lack of research into how it affects insects. Fewer than 25 scientific studies have examined this - far too few, considering the global decline in insect numbers.



<h2 class="wp-block-heading" id="h-a-call-for-smarter-farming">A call for smarter farming</h2>



The team behind the study says it’s time to rethink how fungicides are used in agriculture. Reducing the frequency of spraying could give insect populations a chance to recover. But that requires more research.



“We need field trials to explore options and develop evidence-based guidelines to consider the knock-on effects of fungicides on beneficial insects,” said Professor Ponton.



Next, the researchers will study whether these reproductive problems are passed on to future generations. 



The team also plans to investigate what happens when insects are exposed to combinations of chemicals - something that’s far more common in real-world farming.



The full study was published in the journal <a href="https://royalsocietypublishing.org/doi/10.1098/rsos.250136" target="_blank" rel="noreferrer noopener">Royal Society Open Science</a>.



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