Tag Archives: evolutionary

Ultra-rare merging of two lifeforms sparks exciting evolutionary prediction: ‘We just haven’t noticed’ – Yahoo News Australia

  1. Ultra-rare merging of two lifeforms sparks exciting evolutionary prediction: ‘We just haven’t noticed’ Yahoo News Australia
  2. Scientists Discover First Nitrogen-Fixing Organelle – Berkeley Lab – Berkeley Lab News Center Lawrence Berkeley National Laboratory (.gov)
  3. The Once-In-An-Eon Event That Gave Earth Plants Has Happened Again IFLScience
  4. Two lifeforms merge in once-in-a-billion-years evolutionary event New Atlas
  5. Scientists discover once-in-a-billion-year event — 2 lifeforms merging to create a new cell part Livescience.com

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Borderlands 3 community scores a big win for science: ‘These players have helped trace the evolutionary relationships of more than a million different kinds of bacteria that live in the human gut’ – PC Gamer

  1. Borderlands 3 community scores a big win for science: ‘These players have helped trace the evolutionary relationships of more than a million different kinds of bacteria that live in the human gut’ PC Gamer
  2. Improving microbial phylogeny with citizen science within a mass-market video game Nature.com
  3. Millions Of Borderlands 3 Players Have Helped Microbiome Research Forbes
  4. Millions of gamers advance biomedical research by helping to reconstruct microbial evolutionary histories Phys.org
  5. Popular first-person shooter (FPS) ‘Borderland 3’. The game’s players have revealed the evolutionary.. – MK 매일경제

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Pokémon Horizons: The Series is an evolutionary fresh start for the anime – The Verge

  1. Pokémon Horizons: The Series is an evolutionary fresh start for the anime The Verge
  2. Watch Pokémon Horizons: The Series Now on Netflix Pokemon.com
  3. ‘Pokémon Horizons’ Team Talks Netflix Debut, First Female Protagonist and Saying Farewell to Ash Ketchum Variety
  4. Watch An Exclusive Clip From Netflix’s New ‘Pokémon Horizons’ Series Romper
  5. Pokémon Day 2024: Pokémon Celebrates U.S. Premiere of ‘Pokémon Horizons: The Series’ with Empire State Building Lights Grand Junction Daily Sentinel

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New Discovery Fills Long-Missing Gap in Evolutionary History

The upper jaw of the infant of Yuanmoupithecus. Credit: Terry Harrison, NYU’s Department of Anthropology

The oldest gibbon fossil was discovered in southwest China.

The earliest gibbon fossil has been found by a team of researchers, filling a long-missing evolutionary gap in the history of apes.

The study, which was published in the Journal of Human Evolution, focuses on the hylobatid family of apes, which comprises 20 species of living gibbons that are found throughout tropical Asia from northeastern India to Indonesia.

“Hylobatids fossil remains are very rare, and most specimens are isolated teeth and fragmentary jaw bones found in cave sites in southern China and southeast Asia dating back no more than 2 million years ago,” explains Terry Harrison, a professor of anthropology at New York University and one of the paper’s authors. “This new find extends the fossil record of hylobatids back to 7 to 8 million years ago and, more specifically, enhances our understanding of the evolution of this family of apes.”

The fossil, found in the Yuanmou area of Yunnan Province in southwestern China, is of a small ape called Yuanmoupithecus xiaoyuan. The study’s analysis concentrated on the teeth and cranial specimens of Yuanmoupithecus, which included an upper jaw from a young child who was less than two years old at the time of its death.

An excavation near the village of Leilao in Yunnan, one of the locations where Yuanmoupithecus remains have been found. Credit: Terry Harrison, NYU’s Department of Anthropology

Using the size of the molar teeth as a guide, Yuanmoupithecus was estimated to be close in size to modern-day gibbons, with a body weight of roughly 6 kilograms—or about 13 pounds.

“The teeth and the lower face of Yuanmoupithecus are very similar to those of modern-day gibbons, but in a few features the fossil species was more primitive and points to it being the ancestor of all the living species,” observes Harrison, part of NYU’s Center for the Study of Human Origins.

Ji discovered the child’s upper jaw during a field survey, and by comparing it with modern gibbon skulls kept at the Kunming Institute of Zoology, he was able to identify it as a hylobatid. In 2018, he invited Harrison and other colleagues to work on specimens gathered over the previous 30 years that were housed in the Yunnan Institute of Cultural Relics and Archaeology and the Yuanmou Man Museum.

“The remains of Yuanmoupithecus are extremely rare, but with diligence, it has been possible to recover enough specimens to establish that the Yuanmou fossil ape is indeed a close relative of the living hylobatids,” notes Harrison.

The Journal of Human Evolution study also found that Kapi ramnagarensis, which has been claimed to be an earlier species of hylobatid, based on a single isolated fossil molar from India, is not a hylobatid after all, but a member of a more primitive group of primates that are not closely related to modern-day apes.

“Genetic studies indicate that the hylobatids diverged from the lineage leading to the great apes and humans about 17 to 22 million years ago, so there is still a 10-million-year gap in the fossil record that needs to be filled,” Harrison cautions. “With the continued exploration of promising fossil sites in China and elsewhere in Asia, it is hoped that additional discoveries will help fill these critical gaps in the evolutionary history of hylobatids.”

Reference: “The earliest hylobatid from the Late Miocene of China” by Xueping Jia, Terry Harrison, Yingqi Zhang, Yun Wub, Chunxia Zhang, Jinming Hui, Dongdong Wua, Yemao Hou, Song Li, Guofu Wang and Zhenzhen Wang, 13 September 2022, Journal of Human Evolution.
DOI: 10.1016/j.jhevol.2022.103251

The study was funded by the National Natural Science Foundation of China, the Yunnan Natural Sciences Foundation, and the Strategic Priority Research Program of the Chinese Academy of Sciences. 

The researchers also received access to skeletal and paleontological collections at the American Museum of Natural History in New York and the Smithsonian Institution’s National Museum of Natural History in Washington D.C., among others, in conducting their study.



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500 million year-old fossils reveal answer to evolutionary riddle

Artist’s reconstruction of Gangtoucunia aspera as it would have appeared in life on the Cambrian seafloor, circa 514 million years ago. The individual in the foreground has part of the skeleton removed to show the soft polyp inside the skeleton. Reconstruction by Xiaodong Wang. Credit: Reconstruction by Xiaodong Wang.

An exceptionally well-preserved collection of fossils discovered in eastern Yunnan Province, China, has enabled scientists to solve a centuries-old riddle in the evolution of life on earth, revealing what the first animals to make skeletons looked like. The results have been published today in Proceedings of the Royal Society B.

The first animals to build hard and robust skeletons appear suddenly in the fossil record in a geological blink of an eye around 550-520 million years ago during an event called the Cambrian Explosion. Many of these early fossils are simple hollow tubes ranging from a few millimeters to many centimeters in length. However, what sort of animals made these skeletons was almost completely unknown, because they lack preservation of the soft parts needed to identify them as belonging to major groups of animals that are still alive today.

The new collection of 514 million year old fossils includes four specimens of Gangtoucunia aspera with soft tissues still intact, including the gut and mouthparts. These reveal that this species had a mouth fringed with a ring of smooth, unbranched tentacles about 5 mm long. It’s likely that these were used to sting and capture prey, such as small arthropods. The fossils also show that Gangtoucunia had a blind-ended gut (open only at one end), partitioned into internal cavities, that filled the length of the tube.

These are features found today only in modern jellyfish, anemones and their close relatives (known as cnidarians), organisms whose soft parts are extremely rare in the fossil record. The study shows that these simple animals was among the first to build the hard skeletons that make up much of the known fossil record.

According to the researchers, Gangtoucunia would have looked similar to modern scyphozoan jellyfish polyps, with a hard tubular structure anchored to the underlying substrate. The tentacle mouth would have extended outside the tube, but could have been retracted inside the tube to avoid predators. Unlike living jellyfish polyps however, the tube of Gangtoucunia was made of calcium phosphate, a hard mineral that makes up our own teeth and bones. Use of this material to build skeletons has become more rare among animals over time.

Fossil specimen (left) and diagram (right) of Gangtoucunia aspera preserving soft tissues, including the gut and tentacle. Image credit: Luke Parry and Guangxu Zhang. Credit: Luke Parry and Guangxu Zhang.

Corresponding author Dr. Luke Parry, Department of Earth Sciences, University of Oxford, said, “This really is a one-in-million discovery. These mysterious tubes are often found in groups of hundreds of individuals, but until now they have been regarded as ‘problematic’ fossils, because we had no way of classifying them. Thanks to these extraordinary new specimens, a key piece of the evolutionary puzzle has been put firmly in place.”

The new specimens clearly demonstrate that Gangtoucunia was not related to annelid worms (earthworms, polychaetes and their relatives) as had been previously suggested for similar fossils. It is now clear that Gangtoucunia’s body had a smooth exterior and a gut partitioned longitudinally, whereas annelids have segmented bodies with transverse partitioning of the body.

Fossil specimen of Gangtoucunia aspera preserving soft tissues, including the gut and tentacles (left and middle). The drawing at the right illustrates the visible anatomical features in the fossil specimens. Image credit: Luke Parry and Guangxu Zhang. Credit: Luke Parry and Guangxu Zhang.

The fossil was found at a site in the Gaoloufang section in Kunming, eastern Yunnan Province, China. Here, anaerobic (oxygen-poor) conditions limit the presence of bacteria that normally degrade soft tissues in fossils.

Ph.D. student Guangxu Zhang, who collected and discovered the specimens, said, “The first time I discovered the pink soft tissue on top of a Gangtoucunia tube, I was surprised and confused about what they were. In the following month, I found three more specimens with soft tissue preservation, which was very exciting and made me rethink the affinity of Gangtoucunia. The soft tissue of Gangtoucunia, particularly the tentacles, reveals that it is certainly not a priapulid-like worm as previous studies suggested, but more like a coral, and then I realized that it is a cnidarian.”

Although the fossil clearly shows that Gangtoucunia was a primitive jellyfish, this doesn’t rule out the possibility that other early tube-fossil species looked very different. From Cambrian rocks in Yunnan province, the research team have previously found well-preserved tube fossils that could be identified as priapulids (marine worms), lobopodians (worms with paired legs, closely related to arthropods today) and annelids.

Co-corresponding author Xiaoya Ma (Yunnan University and University of Exeter) said, “A tubicolous mode of life seems to have become increasingly common in the Cambrian, which might be an adaptive response to increasing predation pressure in the early Cambrian. This study demonstrates that exceptional soft-tissue preservation is crucial for us to understand these ancient animals.”

Close up photograph of the mouth region of Gangtoucunia aspera showing the tentacles that would have been used to capture prey. Image credit: Luke Parry and Guangxu Zhang. Credit: Luke Parry and Guangxu Zhang.

The paper “Exceptional soft tissue preservation reveals a cnidarian affinity for a Cambrian phosphatic tubicolous enigma’ will be published in Proceedings of the Royal Society B on Nov. 2.

More information:
Exceptional soft tissue preservation reveals a cnidarian affinity for a Cambrian phosphatic tubicolous enigma, Proceedings of the Royal Society B: Biological Sciences (2022). DOI: 10.1098/rspb.2022.1623. royalsocietypublishing.org/doi … .1098/rspb.2022.1623

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Guardians of the Galaxy Vol. 3’s Villain: Who Is the High Evolutionary? | Comic-Con 2022

We’re blasting off once again, as James Gunn reassembles the Guardians of the Galaxy for Guardians of the Galaxy Vol. 3. The long-awaited-threequel is pitched to round off this cosmic roster of rag-tag rogues, and thanks to San Diego Comic-Con, we finally have confirmation that Peacemaker’s Chukwudi Iwuji will be playing the Marvel character known as the High Evolutionary. (The actor even showed up at SDCC 2022 in costume!)

Fans already knew Iwuji would have a part to play in Vol. 3, with reports indicating he’d appear in the film as a “deeply complex” and “extremely powerful” addition to the Marvel Cinematic Universe. Following in the footsteps of Doctor Strange in the Multiverse of Madness’ Living Tribunal and Thor: Love and Thunder’s Eternity, this cosmic character from the MCU is welcome addition. But just who is the High Evolutionary?

Who Is the High Evolutionary?

Back when Guardians of the Galaxy Vol. 3 started casting, many thought the Vol. 2 post-credits tease of Adam Warlock meant Will Poulter’s character was the villain of the movie. But now it seems the High Evolutionary, who started off as an obscure Thor foe, will be stepping up as this movie’s de facto big bad.

Introduced in 1966’s The Mighty Thor #133 and #134, the High Evolutionary is also known as Herbert Edgar Wyndham. A scientist with a great interest in, you guessed it, evolution, Wyndham’s mission in life is to artificially accelerate mankind’s evolution.

Thor #134

An X-Men Connection

The comics tell us that the High Evolutionary took an interest in the works of Nathaniel Essex – better known as X-Men villain Mister Sinister – but he took things even further.

Much like Essex, Wyndham wanted to perfect human genetics through experimentation, meaning he inadvertently created a race of talking animals called the New Men in his “citadel of science” that was placed in Wundagore. Tying back to the MCU, Mount Wundagore was a major point of interest in Multiverse of Madness, and where we last saw Wanda Maximoff before she may or may not have died (she’s totally not dead, come on). After being abandoned by partner Doctor Jonathan Drew (father of Jessica Drew/Spider-Woman), Wyndham gave himself a suit of silver armor to protect him from werewolves (comics!). This gave the character his signature supervillain look (which Iwuji showcased a variation of at SDCC). The High Evolutionary dubbed his experiments the Knights of Wundagore, and used them to ensure the demonic god Chthon was trapped there (that’s a Wanda Maximoff connection right there).

6 Comics Teased at Marvel’s Next Big Thing Panel at Comic-Con 2022

The High Evolutionary and the Scarlet Witch

The character does have a variety of ties to familiar characters in the MCU. Eventually he was revealed to be the puppet master behind Pietro and Wanda Maximoff’s getting their powers in the comics. The movie franchise has established that Quicksilver and Scarlet Witch gained their abilities via the Mind Stone and experimentation done by HYDRA, but this could still be retconned to include the High Evolutionary.

That said, it seems likely the High Evolutionary of Vol. 3 will connect to Ayesha (Elizabeth Debicki) and her people the Sovereign, who we first met on the big screen in Vol. 2. His evolutionary skills could connect to Ayesha’s creation of Adam Warlock (not to mention any possible revenge plot she might have against the Guardians). Speaking of…

Pietro and Wanda Maximoff’s complicated origin story involves the High Evolutionary.

The Adam Warlock Connection

Back in the comics, having had enough with our Earth, the High Evolutionary established Counter-Earth with the New Men, and then bestowed the Soul Stone to Adam Warlock. But with the Infinity Stones seemingly destroyed in the main canon of the MCU, we’ll have to wait and see whether Gunn has adapted this aspect of Warlock’s origin story.

Eventually, the enormously powerful cosmic beings the Beyonders eventually tricked Warlock into murdering the High Evolutionary. With Secret Wars just announced as the current, uh, endgame of Phases 4, 5, and 6, this could be a significant fact to remember since the Beyonders were a key part of that comics storyline. Could the High Evolutionary stick around for several phases before buying it at the hands of Warlock in that sure-to-be epic?

Of course, in typical style, death was only temporary. Later issues saw the High Evolutionary try to take over Earth and catch the attention of the Avengers. A super-evolved Hercules was sent to stop him, which again could tie to the post-credits tease of Zeus’ son in Thor: Love and Thunder. Hercules and the High Evolutionary eventually evolved themselves out of existence and were imprisoned by the Celestials. More recently, he battled Ultron and Phalanx warriors who wanted to seize Warlock for themselves. Although it looked like Warlock perished, his consciousness lived on and the High Evolutionary knew he’d survive to lead the “new” Guardians of the Galaxy. Given that Gunn said this is “probably” the last time we’ll see the current team, this all sort of fits into place if we’re looking at a brand-new lineup for a potential fourth Guardians movie.

The Cosmic and the Rocket (Raccoon)

The character also has ties to the cosmic side of Marvel, like Galactus and the Silver Surfer, who of course are tightly connected to the Fantastic Four. An FF movie might seem a long way off, but if the High Evolutionary is sticking around for a little longer, we could see the comics story of him draining the Silver Surfer’s powers for himself.

As for where you might’ve seen the High Evolutionary before, he had a small arc in X-Men: The Animated Series, was in Spider-Man: Unlimited, and was then voiced by Nolan North in Disney XD’s Guardians of the Galaxy series.

In that latter story, he captured Rocket Raccoon. And there’s plenty of backstory left to explore with Rocket in the MCU, with the first footage of Guardians 3 from SDCC revealing that we’ll be seeing a young version of the character. It seems pretty clear that the High Evolutionary must’ve played a part in Rocket’s origin (remember all those cybernetic implants on his body?).

Disney’s Star Wars Costumes Make the Jump to Comic-Con

The High Evolutionary has also crossed paths with everyone from Spider-Man’s Dr. Miles Warren (the Jackal) to Hulk, trying to accelerate the latter forward by a million years in evolution. If anything, his abilities as a leading geneticist should at least raise a few eyebrows given a recent X-Men hint in the MCU. The franchise loves a “mad scientist” stereotype, and even if this character’s comic origin isn’t necessarily linked to the Guardians of the Galaxy, Gunn is set to put his own spin on the source material. Whether the High Evolutionary is a one-and-done villain remains to be seen, but either way, fans are ready to welcome Iwuji into the MCU.

What do you hope to see from the High Evolutionary and Guardians of the Galaxy Vol. 3? Let’s discuss in the comments!



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Scientists Analyzed Penguin DNA And Found Something Quite Remarkable

Penguins are no strangers to climate change. Their life history has been shaped by rising and falling temperatures, and their bodies are highly specialized for some of Earth’s most extreme conditions.

 

And yet, scientists are concerned the evolutionary path of the penguin may be grinding to a halt, thanks to what appears to be the lowest evolutionary rates ever detected in birds.

A team of international researchers has just published one of the most comprehensive studies of penguin evolution to date, which is the first to integrate data from living and fossil penguin species.

The research unveils the tumultuous life history of penguins in general, with three-quarters of all known penguin species – now represented by fossils only – already extinct.

“Over 60 million years, these iconic birds have evolved to become highly specialized marine predators, and are now well adapted to some of the most extreme environments on Earth,” the authors write.

“Yet, as their evolutionary history reveals, they now stand as sentinels highlighting the vulnerability of cold-adapted fauna in a rapidly warming world.”

On land, penguins can appear a bit ridiculous, with their awkward waddle and seemingly useless wings. But underwater, their bodies are transformed into hydrodynamic torpedoes that would make any fleeing fish wish it could fly.

 

Penguins had already lost their ability to fly 60 million years ago, before the formation of the polar ice sheets, in favor of wing-propelled diving.

The fossils and genomic data suggest the unique features that enable penguins’ aquatic lifestyles emerged early in their existence as a group, with rates of evolutionary change generally trending downwards over time.

The scientists think penguins originated on a Gondwanan micro-continent called Zealandia, which is now mostly submerged under the ocean.

The paper suggests the ancestors of modern penguins – crown penguins – emerged approximately 14 million years ago, a whole 10 million years after genetic analyses have hinted at.

This particular period would coincide with a moment of global cooling named the middle Miocene climate transition. Living penguins, however, split into separate genetic groups within the last 3 million years.

Penguins spread out across Zealandia before dispersing to South America and Antarctica multiple times, with later groups likely hitching a ride on the Antarctic Circumpolar Current.

The scientists found that almost every penguin species experienced a period of physical isolation during the Last Glacial Period.

 

Their contact with other penguins was limited during this time, as groups were forced to live in more fragmented areas of habitat further north, where they could still find food and shelter.

As a result, the DNA pool of each group became narrower, pushing species further apart genetically.

In the period of warming that followed, they moved back towards the poles, and some groups, now much more genetically distinct, crossed paths once more.

The way certain groups of penguins experienced these significant climate events offers insight into how they might cope with human-caused climate change.

The groups that increased in number when warming occurred shared some features: They were migratory, and foraged offshore. The researchers think these features allowed them to respond to changing climates better, especially the ability to look further afar for prey and to move to lower latitudes.

Those that decreased in number, on the other hand, lived in one particular place, and foraged closer to shore for food: a lifestyle that doesn’t cope too well when the conditions ‘at home’ drastically change.

 

But penguins’ ability to change might be limited by more than just lifestyle – it seems to be embedded in their genes.

It turns out that penguins have the lowest evolutionary rates yet detected in bird species, along with their sister order, Procellariiformes, which includes birds like petrels and albatrosses.

The researchers compared 17 different orders of birds overall, using several genetic signatures closely related to rates of evolutionary change.

They noticed that aquatic birds generally had slower rates of evolution than their terrestrial kin, so they think the adoption of an aquatic lifestyle might go hand-in-hand with low evolutionary rates. They also think that evolutionary rates in birds are lower in cooler climates.

The order Pelecaniformes, which includes seafaring birds like pelicans and cormorants, were a near third for lowest evolutionary rate, and waterfowl (order Anseriformes) had much lower rates than earthbound fowls like turkeys, chickens, and quails (order Galliformes).

The researchers note that the ancestral crown penguins evolved at a faster rate than living penguins, but even then, this was slow compared to other birds.

Half of all living penguin species are endangered or vulnerable, and the scientists say their slow evolutionary rates and niche lifestyles could send penguins towards a dead end.

“The current pace of warming combined with limited refugia in the Southern Ocean will likely far exceed the adaptive capability of penguins,” they write.

“The risks of future collapses are ever-present as penguin populations across the Southern Hemisphere are faced with rapid anthropogenic climate change.”

This research was published in Nature Communications.

 

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Scientists pinpoint the exact moment in evolutionary time when mammals became warm-blooded

Scientists have pinpointed the moment in time our earliest ancestors evolved to be warm-blooded, and it happened much later and far more quickly than the researchers expected.

The discovery, made by studying the minuscule tubes of the inner ear, places the evolution of mammalian warm-bloodedness at around 233 million years ago — 19 million years later than scientists previously thought.

These semicircular canals are filled with a viscous fluid, called endolymph, that tickles tiny hairs lining the canals as the fluid sloshes around. These hairs transmit messages to the brain, giving it instructions for how to keep the body balanced. Like some fluids, the honey-like endolymph gets runnier the hotter it is, requiring the semicircular canals to change their shape so the fluid can still do its job. In ectothermic, or cold-blooded, animals, this ear fluid is colder and thus behaves more like molasses and needs wider spaces in which to flow. But for endothermic, or warm-blooded, animals, the fluid is more watery and small spaces suffice. 

Related: Ancient toothless ‘eel’ is your earliest known ancestor

This temperature-based property makes tiny, semicircular canals a perfect place to spot the moment when ancient mammals’ cold blood turned hot, researchers wrote in a paper published July 20 in the journal Nature (opens in new tab).

“Until now, semicircular canals were generally used to predict locomotion of fossil organisms,” study co-lead author Romain David, an evolutionary anthropologist at the Natural History Museum in London, said in a statement (opens in new tab). “However, by carefully looking at their biomechanics, we figured that we could also use them to infer body temperatures. 

“This is because, like honey, the fluid contained inside semicircular canals gets less viscous [syrupy] when temperature increases, impacting function,” David explained. “Hence, during the transition to endothermy, morphological adaptations were required to keep optimal performances, and we could track them in mammal ancestors.”

To discover the time of this evolutionary change, researchers measured three inner ear canal samples from 341 animals — 243 living species and 64 extinct species — spanning the animal kingdom. The analysis revealed that the 54 extinct mammals included in the study developed the narrow inner ear canal structures suitable for warm-blooded animals 233 million years ago. 

Before this study, scientists thought mammals inherited warm-bloodedness from the cynodonts — a group of scaly, rat-like lizards that gave rise to all living mammals — that were thought to have evolved warm-bloodedness around the time of their first appearance 252 million years ago. However, the new findings suggest that mammals diverged from their early ancestors more markedly than expected.

And this drastic change happened surprisingly fast. Heat-friendly ear canals didn’t just appear later in the fossil record than the scientists expected. It happened far more rapidly, too — popping up around the same time the earliest mammals began evolving whiskers, fur and specialized backbones.

“Contrary to current scientific thinking, our paper surprisingly demonstrates that the acquisition of endothermy seem[s] to have occurred very quickly in geological terms, in less than a million years,” study co-lead author Ricardo Araújo, a geologist at the University of Lisbon in Portugal, said in the statement. “It was not a gradual, slow process over tens of millions of years as previously thought, but maybe was attained quickly when triggered by novel mammal-like metabolic pathways and origin of fur.”

Follow-up studies will need to confirm the findings via other means, but the researchers said they are excited that their work will help to answer one of the longest-standing questions about the evolution of mammals.

“The origin of mammalian endothermy is one of the great unsolved mysteries of paleontology,” study senior author Kenneth Angielczyk, the Field Museum’s MacArthur curator of paleomammalogy, said in the statement. “Many different approaches have been used to try to predict when it first evolved, but they have often given vague or conflicting results. We think our method shows real promise because it has been validated using a very large number of modern species, and it suggests that endothermy evolved at a time when many other features of the mammalian body plan were also falling into place.”

Originally published on Live Science.

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Microscopic mites that have sex on our faces at night could face evolutionary oblivion, say scientists | Science & Tech News

If you think giant pandas had it bad, spare a thought for the tiny parasitic mites that live in the pores of the skin on our faces which may be destined for an evolutionary dead-end, according to a new analysis of their DNA.

More than 90% of us host the 0.3mm long-mites in the oily folds on our faces, most living in the pores near our noses and eyelashes.

It is probably the closest relationship to another animal most of us never knew we had.

The mite, Demodex follicularum, spends its entire lifetime living in our skin follicles. In the daytime they feed on our oily skin secretions, at night they leave the pore to find mates, and find new follicles in which to have sex and lay their eggs.

If the thought makes you want to wash your face, forget it. You’ve been carrying the mites since you were born – they’re passed from mother to baby during breast feeding – and live too deep in the pores to be washed out. And besides, we need them, says Dr Alejandra Perotti of the University of Reading, who co-authored the study.

“We should love them because they’re the only animals that live on our bodies our entire life and we should appreciate them because they clean our pores.”

“Besides, they’re cute,” says Dr Perotti.

Perhaps not everyone would agree. The mites have four pairs of stubby legs each with a pair of claws. Beyond that a long worm like body which, under the microscope, can sometimes be seen protruding from our hair follicles.

But this latest study, published in the journal Molecular Biology and Evolution, has shown just how incredibly intimate their relationship with humans has become.

The researchers analysed the genome of the mites and found it has the smallest number of functional genes of any arthropod (insects, arachnids and crustaceans).

The animals have become so dependent on their human host that their genome is “eroding” — stripped down to the bare minimum of genes needed to survive, the researchers conclude.

They found that the gene which normally regulates waking and sleeping in arthropods has been lost. Instead, the organism detects changes in levels of the hormone melatonin in our skin secretions. It goes up when we sleep, telling Demodex to get up, and goes down when we wake up – their cue to head back down our oily pores for dinner.

They’ve also lost the gene that protects their body’s from UV light – what’s the point when you only come out at night? Even their body plan is minimalist – each leg is powered by just a single muscle cell.

Their ecology becoming so closely synchronised with humans shows the species is on its way from being a parasite to a symbiont – an organism entirely dependent on another for its survival. In this case, us.

As their genetic diversity shrinks, and with it their ability to leave their host and find new mates, they are also at possible risk of eventually going extinct – either when humans do or as a result of some significant change to their environment.

It was once believed Demodex were a cause of common skin conditions, but in healthy people the evidence is Demodex actually help prevent problems like acne by unblocking pores.

But that’s not the only reason we should care about them, says Dr Perotti:

“We are living in a world where we should be protecting biodiversity — and these are our very own animal.”

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A microscopic evolutionary arms race is happening between sperm

In the years since the 1859 publication of “On the Origin of Species,” Charles Darwin’s ideas about evolution have become foundational to the field of biology. Yet though his ideas were revolutionary, Darwin was not all-seeing — and recent scientific work has revealed a missing element in his theories. That missing piece has to do with sperm.

Indeed, beginning in 1970 and continuing full throttle with new research published earlier this year, biology experiments highlighting “sperm competition” among males are filling in some of the blanks left by the great 19th-century evolutionary scientist. As it turns out, there are evolutionary battles raging in microscopic, behavioral, and physical fields. These skirmishes are about the rights and abilities of rival males to impregnate females.

Darwin used the term “natural selection” to describe the ability of genetically lucky organisms to survive long enough to procreate under environmental conditions that kill others. Animals’ supreme and universal urge to send their DNA into subsequent generations drives evolution. Indeed, to them, it is the very meaning of life. Copulation is how animals satisfy their urgent evolutionary impulse. And for almost all species of multicellular animals, procreation requires that sperm meets egg.

In 1871, twelve years after the publication of “Origin,” Darwin’s “The Descent of Man and Selection in Relation to Sex” made clear that getting sperm to meet egg relies on “sexual selection.” By that term, he meant the preference in one sex for certain attributes in the other. For example, male peacocks with spectacularly feathered tails get sexually selected more often to copulate with fertile females than do less well-ornamented males. Stags with big antlers score more often than stags with small ones.

As world-enlightening as Darwin’s ideas of natural and sexual selection were, there’s a tiny whiff of failure about him as a scientist. Brilliant as he was, he never realized that natural selection and sexual selection aren’t quite enough to explain evolution.

The piece of the evolutionary puzzle Darwin missed

In many species, females take more than one mate during a breeding cycle. (The technical term is that they are “polyandrous.”) For males, this means that successfully copulating isn’t a guarantee that they’ve fertilized eggs. A rival might get to those eggs instead.

Some modern scholars consider Darwin’s failure to recognize polyandry as the wrench jamming up the works of evolution to be one of his biggest oversights.

Here are some of the disruptions to the simple “sperm + egg = baby(ies)” equation that polyandry creates. Say, for example, that multiple males have copulated with the same fertile female. Probably at least one of those males will impregnate her.

But which one?

If she’s carrying more than one egg (and some insects carry hundreds), many males might get to be biological fathers. Some males will probably end up fertilizing more eggs than others, and some may not get to fertilize any at all. Usually, a competition of sorts determines who fertilizes what and in what number. The battle can happen on a microscopic scale, with immediate physiological changes to semen and sperm quality. On the other hand, behavioral adaptations may give an animal his needed edge. (Sometimes, to the casual human eye, these behavioral adaptations can seem impossibly weird.) Even physiological adaptations can boost a male’s chances. (Physical adaptations don’t happen on the spur of the moment during sex like physiological changes to sperm do. They evolve over millions of years.)

Dr. Parker noted that, usually, the last male to inseminate before the female drops her sac in dung wins. He becomes the biological father of around 80% of the eggs.

 

As a group, the adaptations are called “sperm competition.” The first evidence of sperm competition was identified by Dr. Geoff Parker of the University of Liverpool. His 1970 research described mating behavior in polyandrous yellow dung flies (Scatophaga stercoraria, common in Northern Hemisphere pastures). Females copulate with many males, all while carrying the same egg sac. Dr. Parker noted that, usually, the last male to inseminate before the female drops her sac in dung wins. He becomes the biological father of around 80% of the eggs.

A male of any species can only make so much sperm in a day or maybe even a lifetime. Since 1970, Dr. Parker and others have found that males in polyandrous species spend sperm prudently. For the yellow dung fly, sperm is best spent on virgins. Some male insects boost their paternity chances by flooding only one female with sperm. Still others spread sperm promiscuously, and so on.

Nursery web spiders

Perhaps because they’re easy to catch and breed, much of the research about sperm competition has been done on spiders. February 2022 work from biologists at Ludwig Maximilian University in Munich and Aarhus University in Denmark shows the benefit to mating males of long copulations. When a male nursery web spider (species Pisaura mirabilis, found all over Europe) offers a female a “nuptial gift” of a silk-wrapped bug, she allows him to copulate. What’s more, she lets him continue to flood her receptacle with sperm for as long as the proffered meal lasts. In an email, co-investigator Dr. Cristine Tuni explained the logic of this adaptation. The spider’s ejaculate doesn’t arrive as a brief, happy burst and then stop. Rather: “In this species, sperm is transferred continuously over time from his copulatory organ into hers,” Tuni says. “So, the longer a male has his organ coupled to a female organ, the more sperm is transferred. The relationship is basically linear.


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One egg sac can carry hundreds of eggs. Because of this, any male wanting a big bang for his f**k probably intuits that size (of the gift) matters. Pumping as much semen as possible can help send his DNA on its way.

Malabar spiders

The Malabar spider (Nephilengys malabarensis, found in Asian rain forests) wields a far more dramatic sperm competition adaptation. Each male has two genital appendages extending from behind the mouth. As semen pulsates out of one, the spider detaches it and leaves it inside the female’s receptacle. Even severed like that, the genital continues to ejaculate. Meanwhile, it also plugs the receptacle, making it difficult for another male to get a genital in. Ready to fend off anyone who tries, the mating male stays on the web near the female. Unfortunately for him, each female’s semen receptacle has two openings. He has only plugged one. This means that, if a rival approaches, the mating male will have to fight fiercely to keep him at bay. To that end, and while ejaculation from the abandoned genital continues, many males eat their only remaining genital.

Of course, that seems like a counter-intuitive strategy. Why get hungry at that very moment? Why hurt yourself right when you may need all the energy you can muster?

A team of biologists from several institutions in Europe and Asia seem to have an answer. They compared the battle survival rates of spiders who’d severed one genital to those of spiders who’d severed one and eaten the other. Additionally, they tested the battle survival rates of genitally intact males. The name of the team’s paper — “Eunuchs Are Better Fighters” — says a lot about why, under duress, a Malabar spider would eat its only remaining genital.

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God knows why that’s true, but apparently it is. What’s more, turning himself into a eunuch is not where a Malabar spider’s sperm competition adaptation ends.

Immediately after mating, a eunuch male usually lets the female eat him. Why not? Doing his best to fulfill his biological imperative to guarantee the intergenerational survival of his DNA, he has left himself incapable of copulating. At least any eggs he has already fertilized will benefit from his calories and protein.

Sperm competition in mammals (including humans)

Coyotes and other canines have an anatomical sperm competition adaptation. A bulbous gland at the base of the penis inflates, locking it inside the vagina and giving ejaculated sperm time to reach the female’s eggs before another male mounts the female. This doesn’t necessarily mean that the first canine’s sperm will fertilize the entire littler. Even so, the arrival time of a canine’s sperm may make a critical difference in whether he can fertilize at least one egg.

In great apes, a primary adaptation is semen volume, which is reflected in testes size. For example, silverback gorillas are not particularly polyandrous. Typically, several females are sexually dominated by a single male. With no need to out-compete the inseminations of other males, gorillas have small testes relative to their enormous bodies.

Female chimps and bonobos, on the other hand, are decidedly polyandrous. Indeed, bonobos are notorious libertines; a fertile female chimp might copulate three or four times an hour with different males. Both males and females copulate with same- and different-sex partners freely and joyfully as a way to have fun, make friends, soothe tempers, and (yes) make babies.

Humans, too, are great apes. In general, women are less polyandrous than chimps and bonobos and more polyandrous than gorillas. Relative to their body sizes, men’s testes are not typically as large as those of chimps and bonobos and they’re not as small as those of gorillas.

In 1993, environmental biologists R. Robin Baker and Mark A. Bellis found one way in which men may have evolved to help sperm meet egg. Testing 35 men, they found that the ones whose mates had recently been out of their sight had more sperm in their ejaculate.

Certainly, many modern humans have intercourse for reasons other than procreation. Providing sexually active people with ways to avoid pregnancy is a multi-billion-dollar industry. Even so, humans’ mating behaviors may be driven to some extent by the same “meaning of life” urge to ensure the survival of their DNA that motivates other animals.

In 1993, environmental biologists R. Robin Baker and Mark A. Bellis found one way in which men may have evolved to help sperm meet egg. Testing 35 men, they found that the ones whose mates had recently been out of their sight had more sperm in their ejaculate. The biologists reasoned from the data that a partner’s temporary absence might make a man uncertain about her fidelity. Niggling suspicion that his sperm has to compete with that of other men might create a physiological response increasing sperm count.

In more recent years, Dr. Leigh Simmons of the Centre for Evolutionary Biology at the University of Western Australia has run a series of experiments with carefully controlled parameters. He and Dr. Sarah J. Kilgallon demonstrated that the very idea of sexual rivals can trigger sperm changes. They showed one group of men pornography involving one woman and two men. A second group saw pornography involving only women. The two researchers found that the sperm produced by men who viewed pornography involving one woman and two men swam faster.

At least one possible sperm competition adaptation in humans is anatomical. Simmons and collaborator Dr. Samantha Leivers have proposed that the piston shape of men’s penises may have evolved to help men rid their mates’ vaginas of a rival’s previously deposited sperm. With a flat-bottomed head and a shaft that is narrower at top than bottom, the human penis can scoop out semen each time it momentarily withdraws from a vagina in preparation for the next thrust.

Males in polyandrous non-human species can ramp up sperm volume, count, and vitality in response to the presence of rivals.

 

Meanwhile, Simmons and many others have acknowledged mate guarding behaviors like sexual jealousy as a primary sperm competition adaptation. Surprisingly, work in the Simmons lab has also demonstrated that mate guarding behaviors like jealousy work against production of higher quality sperm. In 2014 in the peer-reviewed journal PLOS ONE, Simmons and Dr. Gillian Rhodes reported:

We found that men who performed fewer mate guarding behaviors produced higher quality ejaculates, having a greater concentration of sperm, a higher percentage of motile sperm and sperm that swam faster and less erratically.

Score one, perhaps, for the idea that the ideal mate is more courtly than boorish.

Sperm competition adaptations and human infertility

The Urology Care Foundation reports that up to 50% of infertility issues among human couples are linked to problems with male semen.

Males in polyandrous non-human species can ramp up sperm volume, count, and vitality in response to the presence of rivals. For humans, even the thought of polyandry can jack up a man’s sperm quality. Considering all of that, might turning the knob way up on polyandry as a real or imagined stimulus rocket launch the get-up-and-go of any given man’s sperm? Might overt and rampant promiscuity on the part of a woman help her man with his fertility problem?

That’s a bit of a sci-fi scenario, but by email and on Zoom I asked Dr. Simmons what he thought about it. By way of an answer, he told me about a body of work by Drs. Mariana Wolfner (Cornell University), Tracy Chapman (University of East Anglia), and Stuart Wigby (University of Liverpool). It shows that a protein called “sex peptide” in the ejaculate of male fruit flies (Drosophila melanogaster, originally an African species) diminishes a female’s sex drive. This reduces the likelihood that, once inseminated, a female will let additional males try to fertilize her enormous sac of eggs.

Unfortunately for the female of that species, sex peptide shortens her lifespan.

The research to which Dr. Simmons referred raises the specter of unpredictable results for humans of a modern reproductive strategy reaching to ludicrous lengths to boost sperm quality.

That said, there’s probably a second problem with my idea of operatic promiscuity, or at least there’s a problem with asking a well-respected scientist to weigh in on it. Generations of anthropologists have made clear that, across cultures, women sometimes take more than one mate. Even so, most women wanting to conceive take pains to seem to do so as part of a couple, harem, or intentional family. Potential risks to women who use exaggerated promiscuity to boost a male partner’s fertility have not been well-studied. Maybe, given the outré arrangement that would be needed to conduct such an experiment, the risks never will be studied at all.

With no easy sperm competition fixes to the infertility problem that 10 to 15% of American couples face, many couples are unable to revel in the meaning of life as Darwin’s natural selection theory defined it. They might take comfort in the realization that philosophers have wondered, without resolution, about “why life?” for millennia. They might also find comfort — or at least comic relief — in the 1983 Monty Python film, “The Meaning of Life.”

In particular, one of the movie’s songs might help boost moods. Granted, its lyrics aren’t about sperm competition per se. They bash narrow-minded ideas about fertility and masturbation. Even so, “Every Sperm is Sacred” might work as a fertility anthem. It could be sung in biology labs and bedrooms as well as in jungles, on spider webs, and near bowls of fruit everywhere.

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