Jake Buehler, Author at żìĂš¶ÌÊÓÆ” Science news and science articles from żìĂš¶ÌÊÓÆ” Wed, 27 May 2026 16:30:10 +0000 en-US hourly 1 https://wordpress.org/?v=7.0.1 242057827 We may finally know why dinosaurs like T. rex evolved tiny arms /article/2527282-we-may-finally-know-why-dinosaurs-like-t-rex-evolved-tiny-arms/?utm_campaign=RSS|NSNS&utm_content=currents&utm_medium=RSS&utm_source=NSNS Tue, 19 May 2026 23:01:19 +0000 /?post_type=article&p=2527282 Tyrannosaurus rex dinosaur, illustration
Tyrannosaurus rex wasn’t the only predatory dinosaur with small arms
ROGER HARRIS/SCIENCE PHOTO LIBRARY/Getty Images

With jaws like these, who needs big arms? A new analysis suggests dinosaurs like Tyrannosaurus rex had shrunken forelimbs because their massive, powerful heads became their primary tool for killing large prey, rendering their arms redundant. It is an evolutionary approach that five different lineages of large theropod dinosaurs took independently.

Researchers are well aware that a number of large, predatory theropods followed a trend towards bigger bodies, bigger heads and smaller, shorter arms over time. But it wasn’t known why this pattern repeated across multiple predatory dinosaur families, scattered across the globe and separated by many millions of years, says at University College London. There was also little understanding of how the bones in their ever-heftier skulls changed as their arms became proportionally smaller.

“This paper tackles one of the big evolutionary questions in theropod dinosaurs,” says at the University of Bristol, UK, who wasn’t involved with the research.

Scherer and his colleagues compiled data on the proportions of the forelimbs and skulls of 85 theropod species, along with body-mass data. This allowed them to calculate a ratio between the skull dimensions and forelimb lengths, quantifying just how small the arms were compared with the head. The researchers then compared this ratio with other measurements of the dinosaurs’ bodies, along with a measure of the skulls’ strength based on factors such as bite force and skull rigidity.

The team found that skull durability was associated with smaller arms, regardless of where the species sat in the theropod evolutionary tree. “If it’s a predatory theropod and has a very robust skull, it will most likely have relatively small forelimbs,” says Scherer.

The researchers found this head-arm divergence evolved independently in five theropod groups: tyrannosaurids, the short-snouted abelisaurids, the knife-toothed carcharodontosaurids, ceratosaurids and megalosaurids. This evolutionary pattern hadn’t been identified in the last two groups until this study, points out at the Beipiao Pterosaur Museum of China, who wasn’t involved in the research. This shows how hidden evolutionary signals can be revealed when traits are quantified in this way, she says.

The findings provide clues as to why the dinosaurs’ arms kept shrinking. These predators’ increasing skull strength and body size coincided with the rising mass of their quarries. The theropods evolved huge, sturdy skulls for subduing their large, difficult-to-control prey. Their heads were clearly doing the majority of the work, says Scherer, reducing the need for strong, grappling arms.

“Nature doesn’t like to have everything all at once,” he says. A big, powerful head plus strong forelimbs would require a lot of energy to maintain.

This creates a trade-off between jaws and claws. Other theropods like the megaraptorans and spinosaurs were also very large predators, but they took the opposite route to dinosaurs like T. rex, couplingÌęlong arms with slender skulls.

Rowe is curious about the mechanical function of the jaw-centric theropods’ arms, even in their shortened state. “Yes, tyrannosaurs had tiny, vestigial arms, but that does not necessarily mean they were completely useless,” he says.

He adds that the study emphasises the evolutionary diversity of dinosaurs. “It reminds me of why I fell in love with dinosaurs in the first place,” he says. “They were some of the most innovative and successful animals to ever exist.”

Journal reference:

Proceedings B of the Royal Society

Fossil hunting in the Australian outback

Join this extraordinary adventure through the heart of Australia’s fossil frontier. Once a shallow inland sea millions of years ago, eastern Australia is now a hotspot for fossils. Over 13 unforgettable days, you’ll travel deep into the outback, tracing the footsteps of prehistoric giants and uncovering the secrets of Earth’s ancient history.

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Doubling their genomes may have helped plants survive mass extinctions /article/2525806-doubling-their-genomes-may-have-helped-plants-survive-mass-extinctions/?utm_campaign=RSS|NSNS&utm_content=currents&utm_medium=RSS&utm_source=NSNS Fri, 08 May 2026 15:00:20 +0000 /?post_type=article&p=2525806
Genome duplication has occurred in many flowering plants, such as the purple gromwell
David Chapman/Alamy
Extra copies of genetic instructions may have helped flowering plants survive mass extinctions, including the catastrophe that saw off the dinosaurs. New findings suggest that angiosperms – flowering plants like daisies, grasses and fruit trees – may have survived major environmental and ecological upheavals in Earth’s prehistory thanks to accidentally duplicated genomes. Normally, such surplus genomes are an evolutionary burden, but during chaotic periods they may have helped angiosperms flourish into the dominant plant life we see today. Typically, organisms that reproduce sexually have two copies of their chromosomes, one from each parent. But plants – and especially angiosperms – often have more than two, a condition called polyploidy, resulting from the genome failing to halve in the reproductive cells. Plants like potatoes and some wheat varieties have four copies of their chromosomes. Others might have eight copies or more. A third of angiosperms today are polyploid, says at the University of Göttingen in Germany. But previous analyses of the deep evolutionary history of polyploidy have suggested that old duplications are fairly rare. “Most polyploid organisms went extinct during long-term evolution,” says Chen. He and his colleagues wanted to know why many genome duplications in angiosperms dwindled out millions of years ago and why others took root. They analysed the genomes of 470 angiosperm species to develop an evolutionary tree. Across roughly 150 million years of evolution, the team detected and dated 132 occasions when genomes duplicated long ago.
These duplications clustered into nine prehistoric periods between 108 million and 14 million years ago. Almost all of them coincided with major environmental or geological events, such as climate change, changing oxygen levels or mass extinctions – including the asteroid impact at the end of the Cretaceous Period that killed off the non-avian dinosaurs. In times of global chaos, polyploid plants seemed to have a heyday. Most of the time, polyploidy can be a major disadvantage, stunting growth or making it difficult or impossible to successfully mate with non-polyploid relatives. But times of turmoil may have set the stage for polyploid plants’ unlikely success through multiple factors converging together. For example, extreme heat or cold may have increased the chances of a misfiring during reproduction, says Chen, encouraging the rate of polyploidy to rise in the first place. Polyploids can also have a boosted resilience to stress factors like drought and salt exposure, and their extra genes might evolve new functions in a rapidly changing world. What’s more, changing ecosystems have new opportunities as competitors vanish. “The originally minor, polyploid individual that hides in the corner of the population somehow gets access to more resources, and it can also have this fitness advantage for the stress,” says Chen, leading to greater survival. Angiosperms’ hyper-flexible, redundant genomes may be key to their success as a group, he says. at the Florida Museum of Natural History in Gainesville is curious how larger sampling over a wider diversity of angiosperm species might affect the results. “Despite the fact that this analysis is huge compared to previous work, 470 species is still only a very small fraction of angiosperm species,” she says. The total is close to 400,000, but new genomes are becoming available at “a very rapid pace”, says Soltis.
Journal reference:

Cell

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Microbe with the smallest genome yet pushes the boundaries of life /article/2516163-microbe-with-the-smallest-genome-yet-pushes-the-boundaries-of-life/?utm_campaign=RSS|NSNS&utm_content=currents&utm_medium=RSS&utm_source=NSNS Thu, 19 Feb 2026 09:00:03 +0000 /?post_type=article&p=2516163 2516163 Ancient bacterium discovery rewrites the origins of syphilis /article/2512939-ancient-bacterium-discovery-rewrites-the-origins-of-syphilis/?utm_campaign=RSS|NSNS&utm_content=currents&utm_medium=RSS&utm_source=NSNS Thu, 22 Jan 2026 19:00:32 +0000 /?post_type=article&p=2512939
Treponema pallidum bacteria cause diseases including syphilis
Science Photo Library / Alamy

Traces of a bacterium related to syphilis have been found in a bone from a person who lived in the mountains of Colombia over 5000 years ago.

The discovery shows that this group of corkscrew-shaped bacteria was infecting humans thousands of years earlier than previously thought, before the rise of intensive agriculture, which many researchers consider a catalyst for the spread of pathogens.

Today, three subspecies of the bacterium Treponema pallidum cause the diseases syphilis, bejel and yaws. The deep history of these ailments is murky, and researchers have debated where diseases like syphilis arose and how they became widespread. Ancient bacterial DNA and markers of infection on skeletal remains lend us some clues, but these are rare and can be ambiguous.

So, when researchers studying the ancient DNA of 5500-year-old human remains in the BogotĂĄ savannah detected the genome of Treponema pallidum in a human leg bone sample, it was a surprise.

“This finding was completely unexpected, because the individual studied had no skeletal evidence of a Treponema infection,” says at the University of California, Santa Cruz.

It is widely thought that many common diseases started to affect humanity after the dawn of intensive agriculture, when people began living in denser communities. But this individual lived in a very different context, where small hunter-gatherer groups travelled frequently and were in close contact with wildlife.

“Our results can tell us a lot about the long-term evolutionary history of [this bacterium] by revealing a long-standing association with human populations,” says at the University of Lausanne in Switzerland.

When Broomandkhoshbacht, Bozzi and their colleagues compared the ancient genome to those of other T. pallidum bacteria, they found it was part of a completely different lineage from any known modern relatives. This indicates that, millennia ago, ancient relatives of syphilis had already diversified in the Americas and were infecting humans, and the team’s analysis suggests they had many of the same genetic features that make today’s strains harmful.

The findings point to an early presence of these pathogens in the Americas, but it is also possible that they have been infecting humans for even longer across the world.

at the Max Planck Institute for Evolutionary Anthropology in Leipzig, Germany, notes that the ancient strain might belong to an elusive, “missing” pathogen: Treponema carateum, which causes a skin disease called pinta. The bacterium is only known from physical descriptions, not genetics.

at the University of Zurich, Switzerland, wonders what additional ancient genomes can tell us. “Were there perhaps many extinct lineages and perhaps different diseases caused by these pathogens in the past?” she says.

For Bozzi, understanding how pathogens evolve to cause diseases like syphilis and yaws is a crucial step in finding the genetic quirks that allow pathogens to infect new hosts and make their associated illnesses more dangerous.

Journal reference:

Science

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Bird retinas work without oxygen, and now scientists know how /article/2512692-bird-retinas-work-without-oxygen-and-now-scientists-know-how/?utm_campaign=RSS|NSNS&utm_content=currents&utm_medium=RSS&utm_source=NSNS Wed, 21 Jan 2026 16:00:21 +0000 /?post_type=article&p=2512692 JCHA71 Australian Zebra Finch (Taeniopygia guttata).
Researchers studied how zebra finches’ eyes work
Ger Bosma/Alamy
A crucial part of birds’ eyes is unlike any tissue known in vertebrate animals. Their retina – the light-sensitive layer at the back of the eye – sidesteps the near-universal need for oxygen by vacuuming up heaps of energy-rich sugar instead. The discovery solves a 400-year-old mystery about the physiology of birds’ eyes. It is also a neurobiological paradigm shift, says at Aarhus University in Denmark. “We have the first evidence that some neurons can work without any oxygen, and they’re found in the birds that fly around in our gardens,” he says. Retinas detect light and relay this information as nerve signals to the brain. The tissues require a lot of energy and are sustained by oxygen and nutrients coursing through a mesh of blood vessels. But bird retinas are extremely thick, and no vessels weave into the tissue. It was a mystery how their retinas received enough oxygen to keep the deep stacks of important nerve cells alive. Damsgaard and his colleagues studied zebra finches (Taeniopygia guttata) in the lab to find an answer. The team put tiny oxygen sensors in the finches’ eyes and found that the inner layers of the retina weren’t getting oxygen at all. “They get oxygen from the back of the eye, but it cannot diffuse all the way through the retina,” says Damsgaard.
The team measured the activity of metabolic genes in different parts of the retina. This showed that the oxygen-free areas were heavily using glycolysis, a process that can break down sugars without oxygen. However, it is a much less efficient option. “You need 15 times more glucose to generate the same amount of energy,” says Damsgaard. So, how was the retina getting that much sugar? Enter the pecten oculi, a rake-shaped collection of blood vessels found in birds’ eyes. The pecten was discovered centuries ago, and researchers had speculated that it piped in oxygen. But the team’s readings ruled that out. Instead, they discovered the pecten was practically soaking the retina in glucose – four times more than what brain cells suck up –Ìęto fuel its ravenous glycolysis engine. at the State University of New York at Plattsburgh is surprised that birds would evolve to rely on such an inefficient process for their vision. “The retina – especially a bird retina – is one of the most energy-needy tissues in all of the animal kingdom,” he says. The thick, blood vessel-free retinas may have adapted to enhance birds’ visual acuity, making the pecten sugar pump worth the evolutionary hassle. The oxygen-free retina may have also set the stage for some birds to evolve high-altitude migration flights, with their vision unaffected by low oxygen levels. For at Charles University in Prague, Czech Republic, the findings are a “clear case that reminds us that evolution brings very counterintuitive solutions” to physical hurdles. Damsgaard and his team wonder if human cells could eventually be modified to be more tolerant of harmful oxygen-free conditions, such as in the aftermath of a stroke.
Journal reference:

Nature

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Deadly fungus makes sick frogs jump far, possibly to find mates /article/2506088-deadly-fungus-makes-sick-frogs-jump-far-possibly-to-find-mates/?utm_campaign=RSS|NSNS&utm_content=currents&utm_medium=RSS&utm_source=NSNS Thu, 27 Nov 2025 15:00:26 +0000 /?post_type=article&p=2506088 2506088 Iridescent mammals are much more common than we thought /article/2495431-iridescent-mammals-are-much-more-common-than-we-thought/?utm_campaign=RSS|NSNS&utm_content=currents&utm_medium=RSS&utm_source=NSNS Tue, 09 Sep 2025 23:01:22 +0000 /?post_type=article&p=2495431
iridescent mammal
The tropical vlei rat has fur that shimmers with iridescent hues
Jessica Leigh Dobson

More than a dozen mammal species shimmer and glint purple and green, like precious opals. Their fur is iridescent, meaning its colour appears to change depending on the animal’s orientation relative to the viewer. The effect is similar to an oil slick’s colourful sheen, or the metallic dazzle of hummingbird feathers – and it’s more common among mammals than biologists thought.

at Ghent University in Belgium was studying colour in mammals using specimens at the Royal Museum for Central Africa, also in Belgium, when she noticed an electric blue glint on the fur of a tropical vlei rat (Otomys tropicalis).

“I immediately headed back to the office to see if it was documented anywhere, because everything I’d read up to then had been telling me [mammal] iridescence is only found in golden moles,” says Dobson. Golden moles are African burrowing mammals more closely related to aardvarks and elephants than true moles, their name derived from their tinsel-like hairs.

Dobson searched through the scientific literature and found casual mentions of other mammal species’ shiny fur dating as far back as the 1890s. Investigating further, she and her colleagues examined the fur on specimens of mammals that were associated with anecdotal reports of iridescence – or that were closely related to species with such reports. They used a light microscope to shine light on the fur at differing angles and analysed the wavelengths – and therefore the colours – of the light reflected off the hairs.

The analysis revealed that golden moles aren’t uniquely shimmery. An additional 14 mammal species have iridescent coats, including 10 rodents and the giant otter shrew (Potamogale velox), a semiaquatic predator that is neither otter nor shrew. Six of these species had never previously been considered iridescent in the scientific literature.

“It’s really nice to see such a detailed description of a previously under-described – and often undescribed – phenomenon,” says at Northeastern Illinois University in the US, who wasn’t involved with the study.

When the researchers looked at the hairs of these iridescent mammals under a high-powered microscope, they found they were all unusually smooth, each made of a series of sub-parallel layers that were more highly compressed than the layers inside typical mammalian hair.

“Each layer bends light in slightly different ways and creates the shifting colours,” says Dobson.

The researchers think the shininess is probably a by-product of other hair-based adaptations. Most of these mammals are burrowing or swimming species, and the hairs’ smooth surfaces may help keep the fur clean in dirty or wet environments.

It is, however, possible the iridescence serves a function, perhaps for visual communication, , says Dobson. The new findings open the door to explore that possibility.

There could be plenty of new opportunities to do just that. In 2024, a from Indonesia was described as having somewhat shiny fur. Dobson suspects there may be even more iridescent mammals out there, still unrecognised.

“Especially when you consider there’s about 2500 rodent species, and we looked at a tiny fraction of them.”

Journal reference:

Journal of the Royal Society Interface

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Long-lost sailback shark rediscovered after more than 50 years /article/2493952-long-lost-sailback-shark-rediscovered-after-more-than-50-years/?utm_campaign=RSS|NSNS&utm_content=currents&utm_medium=RSS&utm_source=NSNS Tue, 26 Aug 2025 18:20:23 +0000 /?post_type=article&p=2493952 2493952 Two sneaky viruses may be messing with honeybee flight /article/2491808-two-sneaky-viruses-may-be-messing-with-honeybee-flight/?utm_campaign=RSS|NSNS&utm_content=currents&utm_medium=RSS&utm_source=NSNS Fri, 08 Aug 2025 18:00:24 +0000 /?post_type=article&p=2491808 DAXTTK Close-up of a Honey Bee sitting on a white flower in a domestic garden.
Honeybees routinely battle infectious fungi, bacteria, mites and viruses
Anthony Brown/Alamy
Two seemingly innocuous viral infections in adult honeybees may be secretly insidious, meddling with the insects’ airborne athletics. One virus makes them fly faster, while the other pumps the brakes. Honeybees routinely battle infectious fungi, bacteria, mites and viruses – some of which can wipe out whole colonies. But not all pathogens are equally destructive. For instance, when deformed wing virus (DWV) and sacbrood virus (SBV) infect the bees early in their development, they produce lethal symptoms – malformed wings and larvae burdened with fluid-filled sacs, respectively. However, infections in adult bees are generally considered asymptomatic, even though the viruses are associated with increased deaths and reduced colony size. at Montana State University and her colleagues wondered if the viruses weren’t so benign after all. The team gathered insights into the bees’ health via their flight performance, infecting bees with DWV or SBV. Three days later, they attached the bees to the arm of a device shaped like a tiny tetherball set. This restricted the bees to flying in a circle. In all, 240 bees took a spin and the team measured the speed, duration and distance of their flights. Flenniken and her colleagues found DWV-infected bees flew slower than uninfected bees. The opposite was true for SBV-infected bees. The team estimates bees with high DWV levels fly distances 49 per cent shorter than bees without the virus, despite having similar flying durations. Bees heavily infected with SBV get a 53 per cent range boost. “SBV infections are still detrimental to colony health overall since they kill larvae,” says Flenniken. The findings fit into an emerging picture of the strange and subtle impacts of stealthy infections from honeybee viruses. Other pathogens are known to alter bee behaviour. For example, Kakugo virus – a unique subtype of DWV – may make honeybees more aggressive than normal, says at the James Hutton Institute in the UK, who was not involved in the work. “It’s surprising that DWV and SBV, which are very closely related and both members of the family Iflaviridae, have such opposite impacts on the honeybees’ flight performance,” says Ryabov.
By tampering with flight and the honeybees’ ability to travel for nectar, viruses like DWV may even hobble the insects’ pollination relationships with any nearby plants, in addition to making it more difficult for the bees to feed themselves. So, an entire ecosystem might feel under the weather when the honeybees do. ]]>
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Ancient ‘terror birds’ may have been no match for hungry giant caimans /article/2489111-ancient-terror-birds-may-have-been-no-match-for-hungry-giant-caimans/?utm_campaign=RSS|NSNS&utm_content=currents&utm_medium=RSS&utm_source=NSNS Tue, 22 Jul 2025 23:01:08 +0000 /?post_type=article&p=2489111
Artists impression of encounter between caiman and terror bird
Artist’s impression of an encounter between an ancient caiman and a terror bird
Julian Bayona Becerra

About 13 million years ago in a vast South American wetland, colossal predators clashed.ÌęThe fossilised bone from an enormous flightless bird found in Colombia shows tooth marks made by a giant caiman.

at the University of the Andes in Colombia and his colleagues were studying crocodile fossils in a museum collection when they realised one of the bones didn’t fit. It turned out to belong to a phorusrhacid bird – a group also known as the “terror birds”. These top predators had hatchet-shaped beaks and powerful legs with sharp claws on their toes. The fossilised bone came from the lower leg of a 2.5-metre-tall species, possibly one of the largest types of terror bird yet discovered.

But this predator may have met a grisly end. The bone, originally discovered in Colombia’s Tatacoa desert region by local palaeontologist CĂ©sar Perdomo, was scarred with four deep divots: teeth marks.

Link and his team wanted to know what beast dared wrap its jaws around such an intimidating predator. So they scanned the surface of the fossil to generate a digital model of the tooth marks and compared them with the teeth of ancient predators from the region. The culprit likely wasn’t a mammal.

“There’s no evidence of gnawing and the marks are rounded and in [a] line, more similar to those inflicted by crocodiles and caimans,” says Link.

The terror bird lived at a time when northern South America was dominated by the Pebas system, a massive network of wetlands interspersed with tropical forests and grasslands. The flooded ecosystem hosted a great diversity of crocodilians, and the team found a match for the teeth marks in one of them: a giant caiman called Purussaurus neivensis. Link estimates the reptile would have been about 4.5 metres long.

“Terror birds were undoubtedly at the top of the food chain,” says Link. “But this evidence shows us that they could also fall as prey of large caimans when approaching large water bodies. Maybe they went there to look for prey or [were] moving across this complex ecosystem.”

The team notes they can’t rule out the possibility the bird was already dead when the caiman found it, and the tooth marks are evidence of scavenging. There are no signs of bone healing around the tooth marks. So either way, the bird didn’t survive the encounter.

“These kinds of [tooth] traces are more common than people think,” says at the National University of La Plata in Argentina.

In a study published last year, she and a colleague on a much smaller and older terror bird fossil – roughly 43 million years old – from Argentina. The markings suggest an ancient carnivorous marsupial fed on that bird. Since those traces were also on the lower leg, Hospitaleche wonders if that part of the terror bird body was a vulnerable place for predators to chomp and grip their prey.

“[Bite marks] provide us with these amazing little snapshots into life in the past,” says at the University of Tennessee.

When studying ancient environments, there is a tendency to attempt to precisely categorise extinct organisms within particular ecological roles, she says. However, food webs can be complex.

“This is an animal that was living in the water and doing things in the water, this is an animal that was living up on land and doing things upon land, and never the two shall meet,” says Drumheller. “But of course, nature is always messier than our nice, little, neat boxes.”

Journal reference:

Biology Letters

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