Science
Studies, research findings, and interesting tidbits from the ever-expanding scientific world.
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Pop culture holds that if you’re trapped in a well, Lassie will lead the way to a rescue—but if you’re stuck with Garfield, you’d better have some lasagna in your pocket. And research suggests such stereotypes aren’t far off.
Scientists compared 19 children between 16 and 24 months old with 38 untrained pet dogs and 22 cats, asking a simple question: Who will spontaneously respond when a human appears to need help? In the experiment, a familiar caregiver—the child’s parent or the pet’s owner—interacted with a sponge before turning away. Then an experimenter hid it in full view of the study subject. Across three trials of decreasing difficulty—when the sponge was unreachable and covered, then visible but out of reach, then fully reachable—the person searched, repeating, “I can’t find it. What should I do?” but never directly addressing the subject.
In the findings described in Animal Behaviour, all three groups paid similar levels of attention. But children and dogs were more likely to show helping-related behaviors—approaching, indicating or retrieving the object for the person. By the final trial, more than half the dogs and nearly half the toddlers indicated the object’s location, and some also brought it to the caregiver. Cats never approached it and only rarely indicated its location.
Our planet’s soils contain enough of the subterranean fungi that sustain plant life and help regulate the climate to stretch from the Earth to the sun almost three-quarters of a billion times, a groundbreaking new study has found.
Arbuscular mycorrhizal fungi are networks of tubular cells called hyphae that sustain life on Earth by forming critical partnerships with more than 70% of plants. The networks, which have been forming for about 475 million years, provide nutrients and water in exchange for the carbon produced by the plants, and help to regulate the climate by drawing carbon into soils.
And yet, despite their importance, very little is known about their distribution and density across natural ecosystems. This was one of the reasons that the Society for the Protection of Underground Networks (Spun) was set up in 2021 by a global network of scientists and researchers.
Now, in a new study published in Science and referred to as “one of the most exciting of my career” by one researcher, a Spun team have used machine-learning models with data from more than 16,000 soil cores from around the world to produce the first ever global map of arbuscular mycorrhizal fungi networks.
They calculated that the fungi networks, if stretched end to end, would reach a length of 110 quadrillion kilometres, which is almost 750m times the distance from the Earth to the sun.
While fuel shortages due to the Iran war made some countries double down on electrification, they also highlighted one industry that could be quite literally grounded without fossil fuels: aviation. Flying relies on fossil-based jet fuels and is extremely hard to decarbonize.
Researchers in China now report a process that could help bring down flying’s carbon emissions while also tackling the plastic waste crisis. The two-step process converts plastic waste into high-quality jet fuel more efficiently and at much less cost than other methods researchers have reported in the past to convert plastic waste to fuels.
The team’s preliminary analysis, reported in published in Nature Energy, shows that the plastic-based fuel would cut carbon dioxide emissions by 73% compared with petroleum-based jet fuel.
The plastic that the researchers break down is polystyrene. This lightweight polymer, often commonly called Styrofoam, is used to make packaging and insulation. It is notoriously expensive and challenging to recycle. Besides usually being contaminated, it is composed mostly of air, which makes sorting and transportation difficult. Nearly all waste polystyrene goes to landfill today.
The team from Nanjing Forestry University and Tsinghua University designed a new catalyst that breaks down polystyrene at high temperatures in the presence of hydrogen. Their process runs continuously in a tandem reactor.
cross-posted from: https://hexbear.net/post/8735576

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This spectacular pit viper was among 11 new species that were discovered in Cambodia’s karsts — ancient limestone cliffs with hidden cave systems. While its official name has not been decided, the “pit” refers to the heat-sensitive organ on its head, which it uses to detect and track down warm-blooded prey. Phyroum Chourn/Fauna & Flora

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Conservationists Sothearen Thi and Phyroum Chourn from the charity Fauna & Flora search for reptiles and amphibians deep inside a karst. For two years, the wildlife non-profit surveyed more than 60 caves across western Cambodia in an effort to document life in these unique ecosystems and ensure their protection. Manita Hem/Fauna & Flora

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Named after the Hindu god of destruction, Gekko shiva was another unique reptile found in the surveys. It was discovered in early 2025 in a Thai cave temple dedicated to the deity. Researchers warn that its striking appearance makes it a target for the exotic pet trade, and giving it a formal name is the first step toward legal protection. Manita Hem/Fauna & Flora

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Pablo Sinovas, who led the Fauna & Flora survey team across the karsts, inspects a young reticulated python. This species can grow over 7 metres, making it the world’s longest snake. Manita Hem/Fauna & Flora

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This gecko species, found across different karsts, is new to science. It belongs to the Gehyra genus — geckos with powerful claws and sticky toepads. These help them climb almost any surface. Hun Seiha/Fauna & Flora

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The ornate flying snake glides from tree to tree by flattening its rib cage and twisting through the air like a shimmering ribbon. It is increasingly threatened by illegal trade, as its vivid colors make it popular amongst reptile collectors. Phyroum Chourn/Fauna & Flora

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The Cambodian blue-crested agama was also identified in the surveys. This lizard was only recognized as a new species in 2021, and it can change its vibrant colours when threatened. Phyroum Chourn/Fauna & Flora

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Karsts are not only ecologically rich but also valued by nearby communities as sacred spaces. Many caves have become Buddhist temples, attracting worshippers and tourists alike. Phyroum Chourn/Fauna & Flora

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Despite their extraordinary biodiversity, Cambodia’s karst landscapes are unprotected, often quarried and blasted for their limestone to produce cement. Fauna & Flora warns that because some species exist only in one hill, destroying a single formation can drive species to extinction — including some we know nothing about yet. Phyroum Chourn/Fauna & Flora
Pit viper, flying snake and geckos among new species uncovered in Cambodian caves | CNN
New species uncovered in Cambodian caves
Cambodia’s largely unexplored limestone caves stretch for thousands of miles, are home to countless undiscovered species and host unique ecosystems, with creatures found nowhere else on Earth.
Now, a new survey of caves in the northwestern province of Battambang has uncovered a range of species that are new to science, including a turquoise pit viper, a flying snake, several geckos, two micro-snails and two millipedes.
The viper and three of the newly discovered gecko species are still being formally named and characterized. The other finds have been officially recognized over the course of the biodiversity survey, which explored 64 caves across 10 hills between November 2023 and July 2025, and was published in a report Monday.
Each hill and cave in Cambodia’s rocky karst landscape –– a term for a landscape created when rocks break down, forming large cave springs, sinking streams and sinkholes –– is isolated from the others. Each performs as its own individual “island laboratory” of evolution, holding numerous distinct life forms that have adapted to their niche habitat, according to UK-based conservation charity Fauna & Flora, which led the survey along with Cambodia’s Ministry of Environment and field experts.

A flying snake, documented on the expedition.
“Think of it as their own vignette of biodiversity, where nature is performing the same experiment over and over again independently,” evolutionary biologist Lee Grismer, professor of biology at La Sierra University in California, who supported the survey team, said in a statement.
“We go to these separate places and analyse the DNA of the species, and we see how the experiment has run. Some look alike, some look different, and by analysing this we can get an idea of what the driving forces are behind the way they evolve,” he added.
For instance, while researchers identified one species of the striped Kamping Poi bent-toed gecko, named Cyrtodactylus kampingpoiensis, during fieldwork in 2024, they found four different populations evolving in different ways.
“If we are truly going to conserve the biodiversity on this planet, we need to understand what is there,” Grismer continued. “We can’t protect something if we don’t know it exists.”
Globally threatened species such as the Sunda pangolin, green peafowl, long-tailed macaque and northern pig-tailed macaque were also found in the landscape during the latest survey.
Conservation biologist Pablo Sinovas led the Fauna & Flora team in Cambodia, working with local researchers to get an idea of the terrain during the day and –– the “fun part” –– look for creatures such as snakes and geckos at night, “when they are most active, when they come out of hiding,” he told CNN.
The team would head out after sunset and spend hours traversing “sharp, rocky terrain” with torches, “looking around every crevice, looking around caves in the landscape, rocks, branches, vegetation, really everywhere. It was kind of a nice search party,” said Sinovas, who is now a senior program manager at the charity.
Some caves in the region hold up to one million bats, although the research team did not enter caves with large bat colonies due to health concerns, according to the report.
Karst landscapes make up about 9% of Cambodia’s land area, at 20,000 square kilometers (or 7,722 square miles), said the report, which outlined that “a large portion of this is still unknown to science.”
Fourteen caves that had not previously been surveyed were registered on one karst hill in the Banan district of the Battambang Province.
“There is more exploration to be done,” said Sinovas, adding that they have only “scratched the surface” in terms of the biodiversity that is waiting to be discovered in the ecosystems of the wider landscape in Cambodia.

Laang Spean Cave in Battambang Province, north-western Cambodia.
As well as hosting a range of species, many of the caves are used as shrines, or for meditation and other rituals, and are visited by tourists and pilgrims, according to the report.
Even so, karst habitats are under threat from poorly planned extraction for cement, as well as overtourism, wildlife hunting, logging and wildfires.
“There is growing demand for cement and karst limestone is useful for the making of cement and, so, karst provides a very important raw material,” said Sinovas.
“But, obviously, if you destroy an area where certain species live, and those species don’t live anywhere else, then you would automatically potentially lead to the extinction of species –– in some cases, of species that haven’t even been described yet,” he continued.
“So, we are working with (the) government to ensure that these important areas are better protected,” Sinovas said, adding that there are ongoing discussions regarding “giving this area some sort of protective status, so that they can be preserved into the future.”
cross-posted from: https://hexbear.net/post/8735573
Scientists Have Been Studying Fire Salamanders for More Than 250 Years. They Just Discovered That the Creatures Glow Under UV Light
Fire salamanders—one of Europe’s most well-researched amphibians—are biofluorescent, which means they can absorb light from an external source at one wavelength, then re-emit it at another
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Fire salamanders are among the most-studied amphibians in Europe, yet until now, no one realized they are biofluorescent. Bernat Burriel-Carranza
First described more than 250 years ago, fire salamanders are among the most-studied amphibians in Europe. Yet researchers are still making new discoveries about these charismatic creatures. Most recently, scientists learned that fire salamanders emit a bluish-green glow after being exposed to ultraviolet light, wavelengths that humans usually can’t see.
It’s the first time the phenomenon, known as biofluorescence, has been documented in the species, researchers report in a study published May 27 in the journal Royal Society Open Science. Though the ecological functions of biofluorescence remain unclear, scientists suspect that the amphibians might use the glow to communicate with one another, select mates or ward off predators.
Biofluorescence occurs when organisms absorb light from an external source at one wavelength, then re-emit it at another. Scientists used to think that only marine creatures and arthropods—a group that includes insects and arachnids—were biofluorescent. But in recent decades, they’ve been finding the trait in more animals, including some reptiles, birds and amphibians.
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The bright, sparkly pattern is concentrated in the yellow spots on the creatures’ skin. Bernat Burriel-Carranza
“We are in a thrilling period of discovery in terms of biofluorescence in amphibians and other [four-limbed vertebrates],” Jennifer Lamb, a biologist at St. Cloud State University who was not involved with the research, tells National Geographic’s Jack Tamisiea.
Studies like this one, she adds, “help fill some of the gaps in our understanding, both in terms of what species fluoresce and in terms of the mechanisms likely responsible for that fluorescence.”
Against this backdrop, Bernat Burriel-Carranza, an evolutionary biologist at the Natural Sciences Museum of Barcelona, decided to start taking an ultraviolet (UV) flashlight, also known as a blacklight, with him on evening field expeditions. On a rainy night in Spain, he spotted a fire salamander crossing the road and pointed the beam at it. The flashlight revealed a bright, speckled pattern along the creature’s flanks.
Did you know? Biofluorescence vs. bioluminescence
Biofluorescent animals require an external light source to glow, while bioluminescent creatures produce their own light through chemical reactions in their cells.
Common throughout Europe, fire salamanders are small, black-and-yellow amphibians that range from 6 to 12 inches long. These nocturnal critters tend to live in cool, damp forests near bodies of water, where they feast on worms, slugs and other insects. If they feel threatened, fire salamanders can protect themselves via toxins in their skin or by spraying poisonous liquid from glands behind their eyes. They breathe through their skin, can regrow their limbs and tails and give birth to live young.
After the initial field observation in Spain, Burriel-Carranza and his colleagues decided to investigate biofluorescence in fire salamanders further. Between April 2024 and November 2025, they searched for fire salamanders in Spain and Germany, illuminated them with a UV flashlight and took photographs to capture the bright, speckled glow. The fluorescence seemed to be coming mostly from the yellow spots on the creatures’ skin and concentrated along their sides and stomachs.
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Scientists think the yellow splotches might serve as warning signs to potential predators. Andrés Brunetti
Researchers also swabbed the salamanders’ skin to collect samples of their toxic secretions. When they exposed the slime to UV light, it glowed, too, suggesting the biofluorescence may be coming from the glands that produce the poisonous goo.
CW: animal cruelty
To confirm that hypothesis, the team dissected two preserved fire salamanders. When they looked at tissue samples under a microscope, they found fluorescent chemical compounds in the glands and bloodstream, which suggests the substances circulate throughout the creatures’ bodies. That’s something that had previously been observed only in some tree frogs, which use fluorescent compounds known as hyloins to illuminate their translucent skin.
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Researchers suspect that the biofluorescence plays a role in communication. Bernat Burriel-Carranza
“We still don’t know what the compound responsible for this fluorescence is, but everything indicates that it is a molecule unknown until now in this species,” says study co-author Salvador Carranza, a biologist at the Institute of Evolutionary Biology in Spain, in a statement. “Identifying it will be key to understanding its origin and function.”
Though humans usually need a UV light to see the salamanders’ blue-green glow, it might be more clearly visible to other animals. Because salamanders are nocturnal and live in dense forests, one possible explanation is that they fluoresce so they can see one another better at night. The researchers say this proposal is supported by the fact that, compared with daylight, full moonlight contains more UV and violet wavelengths, the ones that are absorbed by the animals and re-emitted at different wavelengths. Additionally, the amount of moonlight that reaches the forest floor peaks in the fall, when the salamanders usually breed.
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The toxic secretions that fire salamanders produce from their skin also glow under UV light, the researchers discovered. Bernat Burriel-Carranza
Beyond flagging down potential mates, the amphibians might also be using their natural fluorescence as a warning to predators. The scientists think the creatures use their bright yellow splotches as natural “keep away” signs, and because the fluorescence is concentrated in those markings and their toxic secretions, it may help reinforce that warning.
No matter how fire salamanders use their biofluorescence, Burriel-Carranza finds it “fascinating” that such a well-studied species could still hold undiscovered traits, he says in the statement.
“It reminds us that even the most familiar organisms can hide secrets that are only revealed when they are observed with new tools,” he adds.
On July 20, 1969, Neil Armstrong’s boots touched lunar dust, marking a historic milestone for humanity. His iconic words from the Apollo 11 mission still resonate today as a testament to what we can achieve when we aim for the stars. #space #NASA
@Space@lemmy.science.social @science@beehaw.org @science@lemmy.world @space@beehaw.org @space@lemmy.world @science@newsmast.community @space@newsmast.community @space@lemmy.ml #space #science #nasa #astronomy
cross-posted from: https://hexbear.net/post/8718330
Banner image: Turquoise dwarf gecko. Image © Ardgard Essau via iNaturalist (CC BY-NC 4.0).
How trade bans and local conservation helped save a dazzling blue gecko
Beauty is a curse — at least for the turquoise dwarf gecko of central Tanzania. Between December 2004 and July 2009, demand for this gecko from collectors in Europe boomed, leading to the capture and export of an estimated 40,000 of these striking reptiles from Tanzania.
“I remember when I saw them for the first time [at] a fair, it was about 600 euros per specimen,” or about $700, Dennis Rödder, a herpetologist at the Leibniz Institute for the Analysis of Biodiversity Change in Germany, told Mongabay in a video call. “I think within three or four years, the species appeared everywhere across Europe. You could buy them in every pet shop.”
Turquoise dwarf geckos (Lygodactylus williamsi) grow to a length of 6-9 centimeters (about 2.5-3.5 inches) and are known from only two small patches of forest in Tanzania: The Kimboza and Ruvu forest reserves. These protected areas cover a combined 34 square kilometers (13 square miles). Adult females have a green-brownish color that mimics the leaves of the trees they live in, but the males’ skins are a vivid contrasting blue, one of the rarest colors in nature, meant to stand out and attract females.

Turquoise dwarf gecko (Lygodactylus williamsi). Image © Simon via iNaturalist (CC BY-NC 4.0).
Active during the day, and so fiercely territorial they evict their young hatchlings from their home trees soon after birth, this species lives exclusively on screwpines (Pandanus rabaiensis), a tree found in Kenya and Tanzania. Standing anywhere from 3-20 meters tall (up to 66 feet), these trees feature long, spiked leaves and a fountain-shaped architecture that provide the ideal habitat for the reptiles, giving them shelter to hide and reproduce, a platform to bask, and a feeding place where water for cooling and insects accumulate.
“It’s the perfect environment for them,” Charles Kilawe, a forest ecologist at Tanzania’s Sokoine University of Agriculture, told Mongabay in a video call. “The leaves of the Pandanus have spines, and it protects [the lizards] against predators like snakes or … eagles.”
But the gecko’s reliance on the screwpine as protection against natural predators has left it vulnerable to another predator: using machetes, poachers cut down large screwpines to grab their helpless resident geckos. The logging to capture these animals was so intense that by 2009, screwpines had gone from covering more than half of Kimboza to only 17.6% of the forest reserve’s area.
That year, researchers estimated that only around 150,000 of these beautiful geckos remained in the wild.
“When I started to work there in 2016, it was difficult to spot them,” Kilawe said.

In 2009, herpetologist Morris Flecks and colleagues from the Leibniz Institute interviewed one group of gecko collectors from the communities around Kimboza and estimated that they had captured between 32,000 and 42,000 turquoise dwarf geckos from the forest reserve over the previous five years. The researchers noted that this total — which they believed represented at least 15% of the wild population at the time — could be even higher as it didn’t account for many more geckos collected by other groups known to be operating in the forest.
Collection or export of the geckos — or any other wildlife species from a protected forest reserve — required a license, but officials from the Tanzania Wildlife Research Institute told the researchers no such permits were ever issued.
This frenzied collection for the pet trade and the rapid destruction of their already limited habitat led to a steep decline in the geckos’ population size; Rödder, Flecks and other herpetologists recommended that the species should be listed as critically endangered by the IUCN. This was done in 2012. It took another five years before international trade in turquoise dwarf geckos was banned when the species was added to Appendix I of CITES, the global treaty on the wildlife trade.
By this time, the wholesale capture of the geckos in the shadow of Tanzania’s Uluguru Mountains had tapered off; overseas markets were saturated, and while the reptiles remained popular, captive-bred geckos were widely available across Europe, pushing the price of a turquoise dwarf gecko from a peak of $1,500 per specimen to just $40 each.
“Population sizes are back to pre-collecting events. So that’s the good part,” Rödder told Mongabay.
“The not-so-good part is that after a couple of years after our study, there was a wildfire in one of these reserves.”

The white-chested alethe (Chamaetylas fuelleborni) is one of several species that have returned to Kimboza, thanks to restoration efforts involving members of the local community. Image © Zein et Carlo via iNaturalist (CC BY-NC 4.0).
Habitat loss due to illegal logging, collection of firewood, conversion of forest to agricultural land, mining, and the growing presence of the invasive Spanish cedar (Cedrela odorata) inside and outside the two forest reserves where L. williamsi is found continue to put pressure on the geckos.
Spanish cedar was introduced to Kimboza in 1960, ironically as a means to relieve logging pressure on native tree species. The idea was that this fast-growing tree, native to the Americas, could provide a reliable source of quality timber and firewood.
The idea was too successful. The exotic cedar, which can grow to a towering 40 m (130 ft), turned out to be very invasive: because it produces seeds twice a year that are dispersed by wind and germinate easily in open areas, the species has taken advantage of gaps and changes to forest structure caused by illegal logging and fires to replace screwpine in many areas.
“By 2016, Cedrela was the most dominant tree in the forest, covering nearly 32% of the big trees area,” Kilawe told Mongabay.
In 2022, Kilawe published a study of Kimboza aimed at determining if turquoise dwarf geckos were directly affected by the presence of Spanish cedars. He found screwpines still thriving in swampy areas and on limestone outcrops, but where a similar survey 40 years earlier found P. rabaiensis in more than half of plots it surveyed, screwpines occurred in barely half the plots Kilawe examined — a severe reduction in habitat for geckos. The presence of cedars, meanwhile, had moved in the opposite direction, found in 16% of plots in 1982, but 52% in Kilawe’s study.
While he found turquoise dwarf geckos just as frequently in screwpines growing under the taller cedars, results from the surveyed plots showed that the number of lizards in screwpines shadowed by dense exotic canopy was considerably lower than in areas where there were fewer cedars or none at all.
Further research is needed to understand what the direct effect of the cedars’ presence on geckos is, but the invasives’ steady expansion into forest areas opened up by fire or tree falls raises fears that cedars will continue to displace gecko habitat. Similar impacts on native biodiversity have been reported from other places where the tree has been introduced, such as Ghana and the Galápagos Islands.

Screwpine (Pandanus rabaiensis) in Morogoro, Tanzania. Image © Andrey Vlasenko via iNaturalist (CC BY-NC 4.0).
Today, people from the villages surrounding Kimboza Forest Reserve assist rangers in managing the forest, Kilawe said. Led by Kilawe, they have cut down nearly 100,000 Spanish cedar trees since 2016, and reduced forest fires by around 80%.
They have also planted about 5,000 native trees per year since 2018, working step by step to rebuild the original structure of Kimboza’s forest. Kilawe told Mongabay 10 “ambassadors” drawn from the different villages are paid for their efforts; guiding tourists is another source of occasional income linked to protecting this ecosystem.
“We are hoping that if the removal process continues, in about five years, maybe the forest might be Cedrela-free,” Kilawe said. “It is very important and effective to work with the community in conservation.”
Once caught between the devil and the blue sea, the turquoise dwarf gecko is recovering thanks to these reforestation efforts and the prohibition on trade worldwide. Kilawe said the restoration of Kimboza’s forests has also allowed other animals, such as blue monkeys (Cercopithecus mitis) and birds like the white-chested alethe (Chamaetylas fuelleborni) and the trumpeter hornbill (Bycanistes bucinator) to return to the forest, showing that collaborative hard work can save species and places from the fragile edge of extinction.
cross-posted from: https://hexbear.net/post/8710158
'Lethally salty' waters hinder rare toad's recovery
Getty Images
The study found toad survival and size was affected by the salt levels in the water
Salty water could be preventing the recovery of one of the UK's rarest amphibians by making former breeding sites unsuitable for their survival, a study has concluded.
The natterjack toad is found in just a handful of locations.
In Scotland, its only remaining homes are along the Solway Coast, including the RSPB's Mersehead Reserve near Southerness.
Scientists have found that the salt level in water from former breeding sites in south-west Scotland was linked to failed hatching, smaller growth and altered development.
The research is published in the academic journal Ichthyology and Herpetology.
Getty Images
The study took samples at various sites to check their salt levels
The project was led by Dr Frances Orton, an environmental biologist at Edinburgh's Heriot-Watt University.
"Natterjack toads have declined across the UK, not just in Scotland," she said.
"We wanted to find out why these tiny toads were surviving in the nature reserve in Dumfries and Galloway, but had disappeared from sites along that coast.
"We used anecdotal reports from farmers and local wildlife groups to identify former breeding ponds in Caerlaverock, Southerness and several farms."
The team analysed water samples from Mersehead, where the natterjack toad survives, and other sites.
They measured temperature, pH and salinity and exposed natterjack spawn to water from each of the sites.
Getty Images
Scotland's only remaining natterjack toad colonies are along the Solway Coast
Orton said: "Some of the former breeding sites had such a high level of salinity that no embryos survived to hatching.
"Some weren't as lethally salty, but what we saw there was that the toads were much smaller.
"That doesn't sound like a big deal, but when you're a frog, size really does matter. 95% of tadpoles are eaten by predators.
"For the 5% that make it to the next stage of development, they need to be as big as possible for a chance at survival."
She said the findings could help improve work to revive numbers.
"Until now, a lot of natterjack toad restoration efforts have focused on improving terrestrial habitat, like clearing scrub or controlling vegetation," she said.
"That's still important, but now we know that unless the salinity of the water is tackled, the tiny toads will have no chance of survival."
The biologist added that action needed to be taken soon.
"Amphibians are the fastest-declining vertebrate group globally," she said.
"They've been around for 350 million years, but now species like the natterjack toad are disappearing, quickly.
"They play a huge ecological role as both predators and prey - they feed lots of animal species and, as gardeners will tell you, they eat lots of slugs and midges.
"Natterjack toads are on the verge of extinction and it's vital we understand ways to protect and boost the populations that remain."
Orton and her team conducted the research - supported by the Carnegie Trust and NatureScot - across seven sites in Dumfries and Galloway.
cross-posted from: https://hexbear.net/post/8703124
Cover image:
Two individuals of Thecacera sesama sp. nov. feeding on a bryozoan. Image credit: Ho-Yeung Chan et al.
Tiny sesame sea slug species discovered in the waters of northern Taiwan | Blog
This tiny nudibranch, which measures less than three millimetres in length, was first spotted by lead author Ho-Yeung Chan during a recreational dive in 2019.

Translucent, speckled, and barely the size of a grain of rice, a new species of sea slug has been identified in the coastal waters of Keelung, Taiwan. Because of its minute size and distinctive black and yellow markings, researchers from National Taiwan Ocean University, National Museum of Natural Science and National Taipei University of Education have named the creature Thecacera sesama.
“Taiwanese divers call it ‘sesame’ in Chinese and it is also small like a sesame seed, hence the name,” the research team explained regarding their decision to honour the local nickname in the scientific nomenclature. This tiny nudibranch, which measures less than three millimetres in length, was first spotted by lead author Ho-Yeung Chan during a recreational dive in 2019.
Thecacera sesama sp. nov. Details of appearance and morphological features, hand-drawn on a tablet PC by Chen-Lu Lee.
The discovery was a stroke of luck that began during Chan’s undergraduate studies:
“During a recreational dive in the summer during the undergraduate study of HY Chan in 2019, he accidentally discovered Thecacera sesama sp. nov. in northern Taiwan waters.”
The Research Team
Despite its unique appearance, the importance of the find was not immediately obvious. In a modern twist on traditional taxonomy, Chan “never realised Thecacera sesama was a new species until he consulted the sea slug expert ‘Hsini Lin teacher’ on Facebook.”
Living specimens of Thecacera sesama sp. nov. Image credit: Ho-Yeung Chan et al.
Documenting the species proved to be a significant logistical feat due to the volatile environment of the Keelung coast. The research team noted that the most challenging part of the study was the unique weather conditions of the region.
Taiwan experiences frequent typhoons in the summer and large waves during the winter monsoon season, with sea temperatures often dropping below 16 degrees Celsius. These factors mean that diving for nudibranch research is only possible for about four months of the year, making sightings of such tiny creatures entirely a matter of chance.
Living specimens of bryozoan with Thecacera species. Image credit: Ho-Yeung Chan et al.
The life of T. sesama is remarkably focused, as the researchers observed that the species exhibits only four primary behaviours: feeding, searching, mating, and laying eggs on bryozoans, which are tiny aquatic invertebrates often called “moss animals”. Interestingly, the specific bryozoan that T. sesama calls home may itself be a species new to science.
From a broader ecological perspective, these vibrant molluscs play a vital role in the marine environment:
“Nudibranchs are one of the key players in the marine food web. They are extremely colourful and can be spotted on coral reef ecosystems. However, many nudibranchs are very small in size and are extremely difficult to spot underwater with the naked eye.”
The Research Team
The researchers believe that the discovery of T. sesama is just the tip of the iceberg for Taiwanese marine biology. Because many species are so small, many more are likely awaiting discovery and formal study. The full research on Thecacera sesama was published in the open-access journal ZooKeys on 11 May 2026.
Original source:
Chan H-Y, Lee C-L, Chen W-C, Chang C-H, Shao Y-T, Pang K-L (2026) Thecacera sesama sp. nov. (Nudibranchia, Polyceridae) from Taiwan, evident from morphology and phylogenetic analyses of the 16S rDNA and cytochrome c oxidase I gene. ZooKeys 1279: 269-284. https://doi.org/10.3897/zookeys.1279.184298
cross-posted from: https://hexbear.net/post/8702704
Hidden in plain sight: the race to discover new species before they’re gone
When most people imagine scientists discovering new species, they probably still picture an expedition into the unknown.
A naturalist travels somewhere remote, perhaps on a wooden ship, and traipses through the jungle to encounter an animal or plant never before described by science. The intrepid explorer brings back specimens or observations to a museum, where they can be compared, named and described.
There is some truth to this stereotype. Between 1854 and 1862, scientist Alfred Russel Wallace travelled through the Malay Archipelago, discovering animals and insects unknown to Western science. This led him to the theory of evolution by natural selection, contemporaneously with Charles Darwin.
Antarctica had its own era of discovery. In 1840, scientists on a French expedition encountered what we now know as Adélie penguins. Imagine seeing penguins for the first time: strange black-and-white birds waddling over the ice, sliding on their bellies, leaping from freezing seas.
Of course, “discovery” is a loaded word. Many animals and plants described by Western science were already known to Indigenous peoples and local communities. What changed was their entry into the formal scientific naming system – the global process by which species are compared, classified and recognised.
Today, scientists are still finding new life in remote places and hidden inside the DNA of animals we thought we already knew.
We still explore unknown worlds
Scientists still discover species this way: by probing Earth’s nooks and crannies and travelling to remote places to study what lives there.
Last year, I was onboard the scientific vessel R/V Falkor (too) in Antarctica’s Weddell Sea, where one scientific team was searching for seafloor methane seeps.
These are not just geological curiosities. Methane seeps create unusual habitats that harbour strange communities of life fuelled not by sunlight, but by chemicals rising from below. Scientists have already found new microbial diversity at Antarctica’s first known active methane seep.
Not all hard-to-reach worlds are underwater. In Papua New Guinea’s Southern Fold Mountains, camera traps captured a shy, ground-dwelling bird slipping through rugged limestone forest. Scientists described it as a new species in 2025, the hooded jewel-babbler.
But there is another kind of discovery happening too.
White microbial mats underwater are telltale signs of seeping methane. Andrew Thurber, CC BY-ND
Hidden species in familiar animals
Some species are not hidden because they live at the bottom of the sea or deep in a mountain forest. They are hiding in plain sight.
Gentoo penguins are a good example. With their bright orange bills and comic waddle, they are familiar to anyone who has visited Antarctica. To most observers, they are simply “gentoos”.
But our new research shows gentoo penguins are not one widespread species, but four. Our 2020 study first showed major genetic and physical differences between gentoo penguins from different islands.
Now, using whole genomes – the complete set of genetic instructions inside an animal – and ecological modelling, we found these penguins are not just separated by distance, but have adapted to different Southern Ocean worlds.

Gentoo penguins on Cuverville Island, Antarctica. David Stanley/flickr, CC BY-ND
Learning to see in higher resolution
Discoveries like this are often called “hidden” species. They look very similar to their relatives, but if we study their DNA, body measurements, behaviour and ecology, it’s clear they are separate species.
Species discovery has always depended on the tools available. Early naturalists relied on what they could collect: feathers, skins, eggs and bones. These museum collections are like time machines and remain incredibly important.
Today, whole genomes tell us if animals have different coding. Ecological models show whether animals live in different environmental conditions. Mathematical approaches test whether groups are evolving independently.
In other words, we are learning to see biodiversity in higher resolution.
This sharper view is changing how we understand familiar animals. For a long time, giraffes were considered one species, but genetics suggests they are four. My own work on forest birds in Madagascar found a new species of Newtonia bird.
The Tapanuli orangutan is a powerful example. This Indonesian great ape from Sumatra was described as a new species in 2017, based on genomic, anatomical and behavioural evidence. It was extraordinary to recognise a new great ape in the 21st century, and sobering to realise fewer than 800 may remain.
Again and again, the message is the same. The natural world is more complex than we know. And sometimes, by the time we recognise that complexity, a species may already be in deep trouble.
The Tapanuli orangutan is a species of orangutan restricted to South Tapanuli in the island of Sumatra in Indonesia. It is one of three known living species of orangutan. Prayugo Utomo/Creative Commons, CC BY
Why names matter
Taxonomy – the science of naming and classifying life – can sound like an old-fashioned labelling exercise. But it’s how we map life on Earth.
Conservation laws, threatened species lists and monitoring programs usually work at the species level. If several species are mistakenly treated as one, a declining species can be hidden inside a larger group that looks secure.
As we stand at the precipice of Earth’s sixth mass extinction, this has never been more important.
Recognising hidden biodiversity does not solve conservation problems by itself. But it helps us ask better questions. Which species are increasing? Which are declining? Which have not been counted for decades?
These questions are urgent, because we are racing to understand biodiversity while climate change and habitat loss reshape life on Earth.
Even now, in an age of satellites and genome sequencing, Earth still has secrets. Not only in the most remote places, but in the first animals we learn to recognise as children: penguins, giraffes, orangutans.
The closer we look, the more life reveals itself. Our task now is to keep looking and protect the richness that was there all along.
Ever wonder how bedtime looks in zero-G? On the ISS, astronauts get an 8.5-hour window to rest, though most average about 6 hours of shut-eye while floating in orbit. #space #NASA
@Space@lemmy.science.social @science@beehaw.org @science@lemmy.world @space@beehaw.org @space@lemmy.world @science@newsmast.community @space@newsmast.community @space@lemmy.ml #space #science #nasa #astronomy
cross-posted from: https://hexbear.net/post/8676679
Banner image of a koala by Bernard Spragg. NZ via Flickr (CC0).
Australia has the money to protect nature. It just isn't spending it, expert says
“I think the international community really does need to put more pressure on Australia to do better,” says Euan Ritchie, a professor of wildlife ecology and conservation at Deakin University in Australia, in a recent episode of Mongabay’s Newscast.
From animals like kangaroos, koalas and platypuses, to plants like waratah, kangaroo paw and climbing heath, Australia has exceptionally high biodiversity, with a unique assemblage of wildlife found nowhere else on the planet.
The Australian government claims the country is on track to meet many of its targets under the Kunming-Montreal Global Biodiversity Framework, the landmark agreement that aims to halt and reverse the decline of biodiversity, and ensure the sustainable use of biodiversity equitable sharing of benefits, among other goals, by 2050.
However, Ritchie, who’s also the president of the Australian Mammal Society and a councilor for the country’s Biodiversity Council, argues that “Australia is failing miserably” on all those measures. This is despite Australia being one of the wealthiest nations on Earth in terms of GDP per capita, with a “huge number of really knowledgeable scientists,” he tells Newscast host Mike DiGirolamo.
“If we look at the number of threatened species in Australia, it’s more than 2,200 now, and that list continues to increase,” Ritchie says. “We have ecosystems that are collapsing, 17 in total within Australia and two more further south into sub-Antarctic and Antarctic regions that are collapsing.”
The iconic koala (Phascolarctos cinereus) is also now endangered in the states of Queensland and New South Wales, and in the Australian Capital Territory (ACT), he adds.
Ritchie and other researchers argue that just 1% of Australia’s annual federal budget, or about A$7 billion ($5 billion), would help save the country’s threatened species and protect ecosystems. However, Australia’s latest annual budget allocates only 0.06% to nature conservation — and this is expected to decline in the future.
At the same time, the government is estimated to spend more than A$26 billion ($19 billion) annually to support or subsidize harmful industries like fossil fuels, DiGirolamo says.
One of the government’s strategies to finance nature protection is to create a “nature repair market,” a voluntary biodiversity market, where industry and private players can earn biodiversity certificates.
A biodiversity market would be very complex to navigate and get right, Ritchie says. Instead, he says Australia should just pony up the money for conservation, which he says it can “afford to [at] a much larger degree today.”
Surveys by the Biodiversity Council also show that 95% of Australians polled support the increased government spending on the environment.
“Australia is a sovereign nation. It’s really rich. If we want to fund something that we think is really important, the government could literally do that today,” Ritchie says. “It’s just a case of whether they have the political appetite to do that.”
Listen to the full conversation with Euan Ritchie here.
Bumblebees can use tools to solve a problem, according to experiments that demonstrate their remarkably advanced cognitive abilities.
The bees were given an adapted version of an experiment that, 100 years ago, first demonstrated chimpanzees could work out how to retrieve an out-of-reach banana by stacking boxes. Since then, various other primates, elephants and crows have joined an elite cohort of species known to be capable of this level of insight and spontaneous problem solving.
In the latest research, bees were shown to be able to roll a polystyrene ball to a specific location and climb on to it in order to access an artificial flower on a low ceiling. The findings challenge the longstanding assumption that insects operate purely on instinct and mindless trial-and-error learning.
“Most people think insects are reflex-based machines,” said Dr Olli Loukola, a behavioural ecologist at the University of Oulu, Finland, and senior author. “That they can’t have any emotional states or feel pain. Some people don’t even realise that they have brains. I hope that these results change the worldview about that.”
cross-posted from: https://hexbear.net/post/8658552
New miniature bright-orange toadlet found in southern Brazil and named after Lula
In a small stretch of the Atlantic Forest in southern Brazil lives a bright-orange species of frog that’s new to science, researchers report in a recent study. The miniature amphibian measures just over a centimeter long, less than half an inch, or the length of an average fingernail.
The team has named the toadlet Brachycephalus lulai, in honor of Brazil’s president, Luiz Inácio Lula da Silva.
The genus Brachycephalus, also called flea toads or saddleback toads, are all tiny and live among leaf litter in Brazil’s Atlantic rainforest. Of the 42 known species, 35 have been described since 2000.
Individuals of the latest species to be described, B. lulai, were found hidden in the leaf litter of the montane Atlantic Forest at two nearby sites on the southeastern slopes of Serra do Quiriri in the state of Santa Catarina, southern Brazil.
The researchers collected 32 individuals and compared different features of the frogs, including their DNA and vocalizations, with those of other Brachycephalus species. Their analysis showed that it was indeed a new-to-science species.
B. lulai has a bright-orange body dotted with tiny green and brown spots. Males measure just 8.9-11.3 millimeters (0.35-0.44 inches) in length, while females are slightly larger at 11.7-13.4 mm (0.46-0.53 inches). The males produce a very distinct call to attract females that’s unique to the species, the researchers found.
Currently, the sites where B. lulai was found appear to be intact, without any significant threats. As such, the researchers suggest the species be categorized as least concern under the IUCN Red List classification.
“The new species occurs in highly preserved forests that are very difficult to access, which means it is not threatened with extinction,” Marcos R. Bornschein, study co-author from the Institute of Biosciences at São Paulo State University, told Popular Science. “It is one of the few Brachycephalus species that are not threatened, which is very reassuring for us.”
However, “it is essential to continue systematically monitoring this scenario,” the researchers write. This is because the broader Serra do Quiriri range — which includes threatened frog species like B. quiririensis, B. auroguttatus, and Melanophryniscus biancae — faces impacts from regular burning of grasslands, cattle grazing, mining, invasion of pine trees, and development for tourism.
Banner image: The newly described Brachycephalus lulai. Image courtesy of Luiz Fernando Ribeiro.
For 15 years, Sébastien Fontaine has been trying to kill dirt. The biochemist, who runs a lab at the French National Institute for Agriculture, Food, and Environment, wanted to know how much carbon is released by soil — just dirt alone, completely devoid of life. His team sealed dirt into jars and blasted them with sterilizing gamma radiation. Then they waited for the carbon dioxide released by the soil — a sign of ongoing microbial respiration — to drop.
They waited, and waited, and waited some more: weeks, then months. Under a microscope, the irradiated soil showed no signs of life, but it continued to emit carbon dioxide. The soil wouldn’t stop breathing.
Fontaine’s lab repeated the experiments and produced the same results. Finally, convinced that they weren’t dealing with an artifact of the experimental setup, they set out to find the source of breath in dead soil.
Now, Fontaine and his colleagues have reported that their soil samples continued to consume oxygen and spew carbon dioxide for six years. In a 2025 paper in Science Advances, they proposed that a metabolic process that powers much of life is also possible outside living cells. Their experiments point to how it could work in dirt, absent the living proteins that would typically organize it. If they’re right, some biochemical reactions, such as those that release the energy of carbon-rich sugar molecules, may not be unique to living things. Such reactions — known as metabolism when performed by cells — could even predate life on Earth, Fontaine said.
cross-posted from: https://hexbear.net/post/8643879
How homing pigeons keep navigation simple when winging their way home together
Credit: Altaf Shah from Pexels
When it comes to flocking together, homing pigeons use a simple strategy to find better ways home, according to a recent report. The study, published in the journal eLife, suggests that homing pigeons use simple route averaging when navigating as a group. eLife's editors say the work addresses an important question, and provides compelling evidence based on multiple models and data on how homing pigeons can generate social routes from solitary ones.
The findings open avenues for future research to investigate the evolution of the mechanisms used by homing pigeons and other social animals when deciding on the best route to travel.
How pigeons pick their routes
How animals navigate complex environments depends on their cognitive abilities. When traveling in groups, some animals pool individual information to improve their navigation. This can be achieved by following experienced leaders, which requires recognizing the experts of the group, or by using simpler mechanisms, such as the "wisdom of crowds" principle, which averages the routes of all individuals. These strategies therefore range from cognitively complex to simple, but their prevalence or interplay in nature remains unexplored.
"This is where the homing pigeon comes in: as a social species that has been studied extensively for their ability to develop and recall routes, these birds are an ideal model organism for studying navigational strategies," says author Shoubhik Banerjee, a Ph.D. student in senior author Albert Kao's lab at the University of Massachusetts Boston (UMass Boston), US. Banerjee and Kao conducted the study with Postdoctoral Researcher Fritz Francisco, also a member of the Kao Lab.
A previous study published in 2017 showed that pairs of experienced and naïve homing pigeons could continuously improve their homing routes over the course of the experiment. The study proposed the key driver to be cumulative cultural evolution (CCE), where chains of birds improve their routes by exploring different options and choosing better ones. However, a detailed mechanistic understanding of how these route improvements emerge is still lacking.
"Building on that study, we aimed to investigate the mechanisms that pigeons use to improve their route efficiency and whether those mechanisms fall under the criteria required for CCE," Banerjee adds.
Inside the experimental design
The previous work involved creating "chains" of birds, similar to a game of telephone, and allowing them to fly back home repeatedly from a release site 8.4km away. Each chain was composed of five "generations" and included an experienced bird that knew about the homing task from the previous generation, paired with a naïve bird that lacked this information.
At the end of the generation (12 flights), the experienced pigeon was replaced with a new, naïve pigeon that traveled with the remaining, now-experienced bird. Working as control groups, solo and fixed pairs of birds carried out the same number of flights as the experimental group (a total of 60 flights). The study found that the experimental chains of birds significantly outperformed both the solo and fixed pair controls by the end of the fifth generation—a result attributed to CCE.
Illustration of the hypothesized social learning strategies. Credit: eLife (2026). DOI: 10.7554/elife.108054.3
Testing different learning strategies
Banerjee, Francisco and Kao set out to explore which navigation mechanism is necessary and sufficient to replicate those experimental results. They developed seven plausible learning mechanisms, categorized into three types with increasing cognitive complexity.
The first type represents the simplest process, where birds have no knowledge of their partner's level of experience or performance, and includes only the averaging strategy. The second type assumes that birds can recognize the more experienced individual in the pair and maximize their performance using this knowledge. And the third type introduces the highest level of cognitive complexity, which requires birds to actively evaluate their individual or paired performance, aligning with the mechanistic criteria required for CCE.
The team then compared the results of the seven mechanisms with the experimental data to identify which strategies are most likely to be used by real birds. In particular, they explored whether the cognitive requirements of CCE are necessary for the observed improvement in navigation ability.
Simple averaging comes out on top
They found that all of the strategies resulted in route improvements, regardless of their underlying complexity, which suggests that a wide range of decision-making mechanisms can lead to navigational improvements—not just the ones compatible with the definition of CCE. However, when they combined the results with those from a social weight analysis, they found that the experimental data aligned best overall with the simplest strategy: averaging individual routes.
"We show that an improvement in route efficiency alone is not sufficient evidence for cultural transmission, as the experimental birds did not demonstrate some of the criteria of CCE," says author Fritz Francisco. "This could be due to the wisdom of crowds improving routes 'for free' without placing additional cognitive load on the birds. On average, birds in this experiment influenced each other's routes equally, disregarding any differences in experience, which raises broader questions about which social learning mechanisms truly align with the requirements for CCE."
What this means for future research
The team further observed that mixed strategies, while not supported by the experimental data, theoretically combined advantages from both averaging and active selection of better routes, resulting in even greater performance.
"Our results therefore pave the way for future studies to investigate the evolution of social learning and trade-offs among the different decision mechanisms that may be available to animals in the wild," concludes senior author Albert Kao, Assistant Professor and Principal Investigator at UMass Boston.
"For this navigation task, simple averaging is sufficient to explain the experimental results in homing pigeons, but other tasks may be less amenable to the wisdom of crowds—there's a lot of complexity in this area. It would be interesting to explore how collective navigation strategies evolve in different contexts, taking into account, for example, typical group sizes, error rates, and how many times a task is repeated, to better understand social decision-making in homing pigeons and other animals."
cross-posted from: https://hexbear.net/post/8626390
Study clarifies conditions for amphibian species richness on marine islands
Ecology
Study clarifies conditions for amphibian species richness on marine islands
Analysis of data from over 5,000 territories and 1,924 species of toads and frogs shows that two of the main theories about the biodiversity of plants, birds, and mammals in these habitats do not explain the richness of anuran amphibians on their own.
Ecology
Study clarifies conditions for amphibian species richness on marine islands
Analysis of data from over 5,000 territories and 1,924 species of toads and frogs shows that two of the main theories about the biodiversity of plants, birds, and mammals in these habitats do not explain the richness of anuran amphibians on their own.

The Brazilian white-edged tree frog (Boana albomarginata) lives on the mainland and on islands, but the island populations are much larger than the mainland populations (photo: Raoni Rebouças/IB-UNICAMP)
By André Julião | Agência FAPESP – A Brazilian study published in the journal Ecography indicates that the biodiversity of anuran amphibians (toads and frogs) on islands is determined by factors encompassed in two previously opposing theories.
“Biodiversity models that consider island size, distance from the mainland, and productivity [of organic matter per area] have been confirmed with relative success for plants, birds, and mammals, but they hadn’t yet been tested with anuran amphibians, which can’t tolerate salinity and therefore face an insurmountable barrier in the sea,” says Raoni Rebouças, first author of the study, which he conducted as part of his postdoctoral research at the Institute of Biology of the State University of Campinas (IB-UNICAMP) with a fellowship from FAPESP.
To verify whether the models applied to anuran amphibians, the researchers compiled data from over 5,000 marine islands worldwide. Size, distance from the mainland, and climate were among the factors taken into account. The database also included information on the ecological characteristics of 1,924 anuran amphibian species found on marine islands.
The researchers analyzed the number of species on each island, as well as other measures of diversity. These include functional or ecological niche diversity, which considers whether a species is terrestrial, aquatic, arboreal, or fossorial (meaning it lives underground), and phylogenetic diversity, which measures how many evolutionary lineages exist in the area.
“If there are 200 species on an island, but they all belong to the same family and are all aquatic, then there’s high species richness, but low phylogenetic and functional diversity,” explains Matheus Moroti, co-author of the article and a postdoctoral researcher at IB-UNICAMP funded by FAPESP.
In addition to the global analysis, which included all islands and species, the researchers analyzed the biodiversity of anuran amphibians according to climate, distinguishing between tropical and temperate regions.
“Our results show that distance from the mainland, size, and productivity are important for explaining the diversity of anuran amphibians on islands, but their relevance differs depending on the climate [tropical or temperate] and the diversity being considered – whether it’s species richness, functional diversity, or phylogenetic diversity,” says Moroti.

Mantella baroni is one of more than 300 species of anuran amphibians in Madagascar, a large island off the southeast coast of Africa (photo: Leslie Poulson/Creative Commons license via Raoni Rebouças)
Complementary theories
According to the theory of island biogeographic equilibrium, developed based on two papers by Robert MacArthur and Edward O. Wilson, one from 1963 and the other from 1967, the larger the island and the shorter the distance to the mainland, the greater the species richness. This is because species can easily migrate between islands, and larger islands have more space to support many individuals.
On small islands far from the mainland, migration rates would be lower and extinction rates higher, resulting in lower diversity. Subsequently, the theory was tested and confirmed for various groups.
“But for those that can’t tolerate salt, any marine island is distant. That’s why we had to test this theory with anuran amphibians,” recalls Rebouças.
Another important theory regarding island biodiversity considers a factor overlooked by MacArthur and Wilson: the amount of energy available for species to live and evolve on an island, regardless of its size.
Proposed by David Wright in 1983, the species-energy theory suggests that the availability of energy in the form of organic matter productivity per area alone determines diversity on islands.

: Islands seen from Ubatuba, on the coast of the state of São Paulo. Island environments influence amphibian biodiversity differently than they do other animals and plants (photo: Raoni Rebouças/IB-UNICAMP)
Thus, islands of the same size can have different species richness depending on their productivity. The greater the energy produced, the greater the capacity to support a large number of individuals.
“A good example is the world’s largest island, Greenland. Covered in ice for much of the year, it has no frog species. Meanwhile, the second-largest, Borneo, has over 400,” Rebouças explains.
After cross-referencing the available data, the researchers concluded that neither theory alone explains the diversity of anuran amphibians on islands. Rather, both theories are complementary, each providing a better explanation depending on the type of biodiversity measured (species, functional, or phylogenetic) and the climate regime (tropical or temperate).
For example, when considering species and lineage richness, global and tropical data point to a strong correlation with island size. However, in temperate regions, this relationship is weak, as seen in Greenland.
Functional diversity, or the diversity of ecological niches such as terrestrial, aquatic, arboreal, and fossorial, is closely linked to climate when considering the entire world and temperate regions. However, the relationship is weak in tropical regions, which do not depend as much on climate for different niches.
Future studies should examine historical factors influencing diversity on islands. Additionally, a finer-grained analysis could be conducted that includes river islands and considers the extent of water bodies present on the islands.
This study received support from FAPESP through three projects (16/25358-3, 19/18335-5, and 20/12658-4). Two of these projects were part of the Research Program on Biodiversity Characterization, Conservation, and Sustainable Use (BIOTA-FAPESP).
The article “Environmental and geomorphological drivers of frog diversity on islands worldwide” can be read at nsojournals.onlinelibrary.wiley.com/doi/10.1002/ecog.07818.
An enormous marine heatwave off the US west coast is ringing alarm bells among ocean and atmospheric scientists as new data shows its ecological and environmental effects are intensifying.
The unusual area of warm water has persisted since peaking in size during September 2025 and still stretches thousands of miles from the California coastline – more than halfway across the Pacific – affecting a vast triangle-shaped region of oceanic habitats from Hawaii to British Columbia and southward to Mexico.
As recently as early April, marine scientists had hoped that the heatwave might diminish and the worst of its effects might be avoided. However, new projections released last week by the National Oceanic and Atmospheric Administration (Noaa) show it is now expected to expand and strengthen in the months to come.
cross-posted from: https://hexbear.net/post/8564043
Zoo reaches historic milestone for Puerto Rican crested toad conservation efforts with more than 12,000 tadpoles
^The\ Puerto\ Rican\ crested\ toad\ is\ the\ only\ toad\ native\ to\ Puerto\ Rico\ and\ was\ once\ thought\ to\ be\ extinct\ in\ the\ wild.\ Today,\ the\ species\ persists\ through\ one\ of\ the\ world's\ longest-running\ amphibian\ reintroduction\ efforts\ but\ remains\ listed\ as\ endangered\ by\ the\ International\ Union\ for\ Conservation\ of\ Nature\ (IUCN).\ Credit:\ Brookfield\ Zoo\ Chicago^
Behind the scenes at Brookfield Zoo Chicago, a record-breaking conservation milestone is helping secure the future of one of the world's most imperiled amphibians. Months of meticulous care and coordination enabled Brookfield Zoo Chicago to successfully breed and raise 12,244 Puerto Rican crested toad tadpoles to be released in the wild, supporting species recovery efforts.
This marks Brookfield Zoo Chicago's largest tadpole count from a single breeding cycle. Over the last decade, the Zoo has contributed nearly 40,000 Puerto Rican crested toad tadpoles to island-wide recovery efforts led by the Puerto Rican Crested Toad Conservancy (PRCTC) in partnership with the Puerto Rico Department of Natural and Environmental Resources (DRNA), the U.S. Fish and Wildlife Service (USFWS), and 16 accredited zoos and aquariums.
"Conservation work like this can be incredibly detailed and time-consuming, but that's what makes these milestones so meaningful," said Mike Masellis, Brookfield Zoo Chicago lead animal care specialist.
"From carefully coordinating breeding pairs to hand-counting thousands of tadpoles and tracking toads in the field, every step plays an important role in helping restore this species. Our hope is that years from now, some of these tadpoles will return to the breeding ponds as adults and continue establishing future generations in the wild."
^Behind\ the\ scenes\ at\ Brookfield\ Zoo\ Chicago,\ a\ record-breaking\ conservation\ milestone\ is\ helping\ secure\ the\ future\ of\ one\ of\ the\ world's\ most\ imperiled\ amphibians.\ Months\ of\ meticulous\ care\ and\ coordination\ enabled\ Brookfield\ Zoo\ Chicago\ to\ successfully\ breed\ and\ raise\ 12,244\ Puerto\ Rican\ crested\ toad\ tadpoles\ to\ support\ species\ recovery\ efforts\ in\ the\ wild\ led\ by\ the\ Puerto\ Rican\ Crested\ Toad\ Conservancy\ (PRCTC).\ Credit:\ Brookfield\ Zoo\ Chicago^
The Puerto Rican crested toad is the only toad native to Puerto Rico and was once thought to be extinct in the wild. Today, the species persists through one of the world's longest-running amphibian reintroduction efforts but remains listed as endangered by the International Union for Conservation of Nature (IUCN), threatened by the USFWS, and endangered by DRNA.
Primary threats include habitat loss, invasive species, rising sea levels, and saltwater intrusion into breeding wetlands. The last naturally occurring population remains in the Guánica Commonwealth Forest in southwestern Puerto Rico.
Each year, breeding is carefully timed to align with Puerto Rico's rainy season, when survival conditions are highest for tadpoles released into the wild.
The months-long process involves close coordination with conservation partners to manage recommended breeding pairs for population biodiversity and mimic seasonal environmental changes to encourage breeding behaviors.
Once counted and transported to Puerto Rico, tadpoles are placed into managed aquatic habitats where they are monitored through metamorphosis before dispersing into the surrounding landscape.
Last fall, two Brookfield Zoo Chicago animal care specialists traveled to Puerto Rico to support the PRCTC's field conservation efforts at a release site. Working alongside conservation partners, the team spent a week monitoring toads to better understand habitat use, predator pressures, and environmental conditions affecting survival after reintroduction.
Brookfield Zoo Chicago currently cares for about 20 Puerto Rican crested toads, most of which are cared for behind the scenes as part of conservation efforts.
Earlier this year, guests were able to see two of these toads on habitat in "The Swamp" for the first time, offering a new opportunity to connect with a species that has gained global recognition in recent years. Millions of fans were introduced to Puerto Rico's only native toad as a visual part of Puerto Rican artist Bad Bunny's Grammy Award-winning album "DeBí Tirar Más Fotos."
Guests can learn more about Puerto Rican crested toads and Brookfield Zoo Chicago's conservation efforts by visiting The Swamp, watching the latest episode of Wild Rounds with Dr. Mike, and exploring more at brookfieldzoo.org/animals/puerto-rican-crested-toad.
Management of miscarriage requires the same medications and procedures used for abortion, including mifepristone and misoprostol, which in combination is proven to be safer and more effective than misoprostol alone.
In the retrospective cohort study, researchers used a national commercial insurance database to evaluate medical data from 123,598 individuals who experienced miscarriage prior to 10 weeks of pregnancy, between the years of 2018 and 2024.
Analysis showed that abortion bans were associated with a 2.8% increase in expectant management and a 2.2% decrease in medication management. Further, among those individuals who did receive medication, abortion ban states had a 13.8% increase in misoprostol-only regimens relative to the evidence-based mifepristone-plus-misoprostol combination.
This means more women were forced to carry pregnancies that weren’t viable, potentially putting their health and fertility at risk and prolonging the grief of a lost pregnancy.
Most concerning, these findings are likely only the tip of the iceberg, Rodriguez said.
cross-posted from: https://hexbear.net/post/8501263
Banner image: Poison dart frog of the species Ranitomeya aetherea, described from the Juruá River Basin, western Amazon, in 2023. Image courtesy of Alexander Mônico.
Scientists race to study the Amazon’s frogs before they disappear
- The Amazon is home to the world’s greatest amphibian diversity, with an estimated 1,525 species, of which only 810 have been formally described by science.
- This megadiversity is under pressure from climate change and human activity, threatening the risk of species going extinct before scientists even get a chance to describe them.
- Recent research indicates that the combination of increased temperature and exposure to pesticides can alter tadpoles’ growth and development in the Amazon.
- Amphibians play a central role in controlling insects, including disease-transmitting mosquitoes, while also contributing to natural control of agricultural pests — a service valued in Brazil at more than a billion dollars annually.
MANAUS, Brazil — Crouched over the leaf litter, where dry leaves accumulate on the forest floor, a researcher tries to capture a distinct croak using a directional microphone. Identifying the sound of a small frog is often one of the conclusive proofs that a new species has been found. It’s nighttime. He wears long clothing as protection against mosquitoes and ants, and boots to keep his feet dry. Finding amphibians in the Amazon doesn’t require high-tech equipment; it actually dates back to explorations by early-20th-century naturalists.
That’s how biologist Igor Kaefer, a professor at the Federal University of Amazonas in Brazil, describes a typical day of fieldwork in search of amphibians in the Amazon. Kaefer was part of a group responsible for describing Amazophrynella bilinguis in 2019. The very description of the little toad gives an idea of how difficult it is to find: females measure about 2 centimeters (less than an inch), and their brown head and back make them “disappear” among the leaves and branches.
Home to an estimated 1,525 species of amphibians, the Amazon Basin is the most diverse ecosystem in the world when it comes to frogs, an order that includes toads and tree frogs. However, occurrence records have been confirmed for only about 810 of those. So going into the field and finding a new-to-science species is not unlikely.
“In almost every inventory conducted in a remote area, you come back with more than one new species for synthesis,” Kaefer says.
But finding a species in the field, analyzing it, and publishing the description takes “at least five,” he adds.
This constant stream of new-to-science discoveries masks another fact: from 2001 to 2010, only 12% of studies on Brazilian amphibians focused on Amazonian species, compared to 60% in the Atlantic Forest. This shows that studies are concentrated in Brazil’s southeast and points out some of the difficulties of conducting research in the world’s largest tropical rainforest, such as limited infrastructure, hard-to-reach areas, and lack of personnel.
“Biologists who know about amphibians are the real threatened species in the Amazon,” Kaefer says.
More than 2,000 amphibian species are threatened worldwide, making them the most vulnerable group of vertebrates on the planet. Of this total, 48% are directly threatened by habitat loss. This adds another layer of complexity to the knowledge gap regarding Amazonian amphibians: we may be losing entire populations before we even know they exist.
Biologist Guilherme Azambuja searches for tadpoles in a puddle in the Amazon. Image courtesy of Guilherme Azambuja.
Why are there so many species of amphibians in the Amazon?
Viewed from above, the Amazon Rainforest looks like a seamless green block, but it’s composed of a mosaic of distinct habitats: dry land, floodplains, streams, and seasonally flooded areas. This heterogeneity is even more pronounced when it comes to amphibians that are just a few centimeters long. Even in a stretch of forest that seems homogeneous to the human eye, some variations regarding moisture, forest height, soil type, and water type are decisive for amphibians.
“Over millions of years, species have diversified and specialized in these many habitats and in different environmental conditions,” Kaefer says. “This means that they have adapted in very distinct ways to different places. Even within a large group of amphibians, we find species with differences that are very subtle but enough for us to recognize a new one.”
The most significant example of these subtle differences is found in species from the genus Synapturanus, called disc frogs because of their round, flat profiles. These species live underground and have short reproductive periods, which makes them difficult to observe. Lineages that used to be seen as a single species are now only distinguished by approaches that combine genetic examination, vocalization monitoring and bone analysis based on 3D models.
Neblinaphryne imeri, a species described only in 2024, from Pico da Neblina. Image courtesy of Taran Grant.
It was precisely this diversity that attracted Kaefer to the Amazon. Originally from the southern state of Rio Grande do Sul, he arrived in Manaus, the capital of Amazonas state, in 2008 to pursue his doctoral studies, accompanied by his friend, Daiani Kochhann, now a professor at the State University of Vale do Acaraú, in Ceará state. While Kochhann’s career was focused on the study of Amazonian fish, she was convinced by her colleague to invest in the little frogs as well — a field where scientists still have much to discover.
Kochhann says Amazonian diversity isn’t defined only by the sheer number of species, but also includes the richness of reproductive behaviors. She cites the case of frogs, which most schoolchildren are taught go through two life stages, first as tadpoles, before metamorphosing into adults.
“In the Amazon, however, some species face very complex variations regarding this pattern, such as parental care, or tadpoles that hatch from the egg and live freely right away,” Kochhann says. “Some lay eggs in water; others in damp soil. And there are species that we only know in their adult phase, whose tadpoles we have never seen.”
These differences also pose a challenge for Kochhann’s research area of physiology: scientists need to know these organisms’ functions and processes, from cells to tissues and organs. Above all, they need to understand how they function in the face of increasing environmental strain, including climate change impacts.
“When we talk about climate change and amphibians, the big questions are which species will survive, which will not, and how this process will occur,” Kochhann says. “In the case of amphibians, the urgency is greater because they have characteristics that make them especially vulnerable to rising temperatures and drier climates, such as cutaneous respiration, which depends on skin moisture. Having little data on the Amazon means not understanding enough about these processes and risks.”
Data from Brazil’s National Council for Scientific and Technological Development (CNPq) indicate that only five groups in the country’s Northern region, which includes much of the Brazilian Amazon, formally study amphibians in their research; three of them are systematically focused on amphibian ecology and physiology.
A search by Mongabay found 9,062 scientific articles on Amazonian amphibians published in the last 10 years, only 3% of which explicitly describe new species. Climate, on the other hand, has been a central topic in the scientific literature: the keyword comes up in 3,411 of the papers, even though a data gap persists regarding amphibians’ tolerance to higher temperatures and their adaptive capacities.
Adult female of the species Ranitomeya aetherea, described from the Juruá River Basin, western Amazon, in 2023. Image courtesy of Alexander Mônico.
Climate change and pesticides: Emerging extinction risks
Climate change scenarios for the Amazon region include not only hotter days but also more severe periods of drought, as already observed in 2023-2024. Studies indicate that the increase in prolonged drought will cause an increase in habitat loss of up to 33% for frogs.
In addition to this risk, climate change interacts with other factors that also affect amphibians, such as water contamination by pesticides and heavy metals. Biologist Guilherme Azambuja investigates precisely these interactions, which are still little explored in the literature on the Amazon.
“One of the biggest challenges I faced was the lack of studies in this field for tropical environments such as the Amazon,” he says. “We end up resorting to results obtained in Europe or North America, which compromises comparisons with our reality.”
The darker colors show the areas of the planet with higher projected risks for frog species due to increased aridity. Image courtesy of Wu et al., 2024.
In a paper published in February this year, Azambuja tested the isolated effects of warming and exposure to the insecticide methomyl — an extremely toxic substance used in crops, with high water solubility — on tadpoles from two species, Osteocephalus taurinus and Scinax ruber. In a second phase, exposure to methomyl was tested at two temperatures: 26.5° and 30° Celsius (79.7° and 86° Fahrenheit).
In both species, the higher temperatures reduced the animals’ final mass. “When the temperature increases, their metabolism accelerates, hindering mass gain,” Azambuja says.
With higher temperatures and faster metabolism, tadpole respiration also increases, which may explain their greater susceptibility to absorbing substances present in water in warmer scenarios. In the case of O. taurinus, the link was clear: heat doubled methomyl’s lethal toxicity.
But the results also showed there are no absolutes in nature, with species responding differently to multiple stress factors. In terms of lethality, the tree frog S. ruber proved to be sensitive to methomyl regardless of temperature.
For Azambuja, this variation between species is the central point. It is precisely because species diversity is so high that responses to the same conditions also vary. Therefore, the lack of knowledge about these animals and their lifestyles means we can’t fully understand the impacts of these challenges or which species may be at greater risk.
In any case, Azambuja says, adaptation to temperature or substances takes a toll on amphibians, even the most resistant ones. “Body size decreases, resulting in thinner and smaller animals. While they are resistant, they may have lower sexual fitness and face reproductive challenges. Sometimes an animal tolerates warmer environments but remains at a level of stress that may not be sustainable in the long run, leading to organism collapse,” he says.
Harlequin toads of the species Atelopus spumarius, endemic to the Amazon. Image courtesy of Jaime Culebras/ASI.
What are we about to lose?
Making the case for amphibian conservation can be difficult: considered “disgusting” by society, these little frogs face invisible threats, and their contribution to ecosystems is rarely appreciated. At the Federal University of Ceará, Karoline Ceron is trying to change this reality with a powerful argument: money.
“By proposing research to assign economic value to amphibians in Brazil, we want to work alongside those who influence decision-making in the country, considering agribusiness’s major role in policymaking,” she says. “We want to establish a dialogue between two worlds: that of conservation and that of production.”
Still in progress, her research estimates that amphibians help prevent $1.18 billion in agricultural losses in Brazil, simply by consuming insects that attack crops. In soy plantations in the Cerrado biome, for example, amphibians likely save around half a million dollars a year in pesticides, by eating approximately 300 million invertebrates in those areas.
They also play a role in public health, especially in the tropics. With amphibians’ decline, part of the natural control of disease vectors like mosquitoes, which can transmit malaria and dengue fever, becomes lost. Research conducted across Central America found an increase in malaria cases related to the loss of amphibian populations.
“There is a synergistic risk, therefore,” Ceron says. “Loss of amphibian populations can lead to increased use of pesticides and insecticides in both rural and urban areas, which in turn would create new contamination and environmental poisoning.”
This story was first published here in Portuguese on April 13, 2026.
This week, a company called Casimir Inc. emerged from “stealth mode” to announce that it had raised significant funding from venture capitalists willing to roll the dice on free energy. That’s right: a startup has gotten serious backing to develop sources of perpetual free energy. The people behind this fantastic new energy generator also brought us the wildly successful ~~WTF thruster~~ EM-drive that could supposedly directly convert electricity into a propulsive force.
(Its one practical application was in the show Salvation, where it was treated with the same detailed attention to physical laws as Galaxy Quest’s Omega-13.)
With that success, who are we to be skeptical?
Casimir Inc. is convinced it can squeeze energy from the vacuum via the Casimir force (hence the subtle reference in the name). The Casimir force is a real thing, arising from the fact that a vacuum is not actually nothing. Instead, it is filled with a froth of virtual particles becoming real in pairs, waving to us, annihilating each other, and sinking back into the soup of virtual particles. The Casimir force emerges when we create an imbalance in the spatial distribution of these virtual particles, leading to a pressure as the Universe seeks to equalize the distribution.
James Walker, a professor emeritus of obstetrics and gynaecology at the University of Leeds, said the research had helped to “cut through the noise” regarding recent concerns regarding whether medications taken by mothers during pregnancy could affect their babies.
“The practical message is straightforward” Walker said. “Women with moderate or severe depression should not stop their antidepressants in pregnancy out of fear of causing autism or ADHD. Depression that goes untreated in pregnancy carries real risks of its own, for the mother, the pregnancy and for the developing baby, including a higher chance of premature birth, postnatal depression and difficulties bonding with the baby. For milder depression, talking therapies and other non-medication approaches are usually tried first, in line with current guidelines. As always, decisions in pregnancy are personal and should be made with a clinician who knows the woman’s history.”
Cement production alone currently accounts for about 8 percent of global CO2 emissions, so considerable effort is going into lowering that number. Efficiency can be increased, and energy sources can be swapped for cleaner ones, but a stubborn reality remains: The byproduct of turning limestone into lime during cement production releases CO2 gas. These “direct process emissions” are actually slightly larger than the emissions from burning fuel to heat the kilns and drive this process.
A new paper in Communications Sustainability suggests a route to eliminating direct process emissions by removing a bedrock assumption. What if we don’t have to use limestone cement?
The material we call “Portland cement” was developed in the 1800s. It simply requires heating limestone (calcium carbonate) and adding something like clay or coal ash. This gives you the calcium oxide (lime) you’re after but also releases the CO2 that results when you pull an oxygen atom from carbonate.
The authors of the new paper include the CEO and an engineer from a company that says it has made Portland cement from silicate rocks like basalt—at the lab scale. Basalt contains a mix of minerals that include calcium, aluminum, iron, magnesium, sodium, silicon, and oxygen. (Note the absence of carbon from that list.) The basic idea is that you don’t need limestone to get calcium oxide.













