Hubendickia lancangensis

Researchers have discovered that a mysterious microscopic creature - from which <a href="https://www.earth.com/news/can-we-prevent-a-catastrophic-meltdown-of-the-worlds-largest-ice-sheet/">humans</a> were thought to descend - is part of a different family tree altogether. Saccorhytus shares the primitive feature of a large mouth surrounded by spines and holes of the deuterostome group, from which our own deep ancestors emerged.



However, a new analysis of 500 million year old fossils from China has shown that the holes around the mouth are bases of spines that broke away during the preservation of the fossils, revealing the evolution of the microfossil Saccorhytus.



“Some of the fossils are so perfectly preserved that they look almost alive,” said Professor Yunhuan Liu of Chang’an University in China. “Saccorhytus was a curious beast, with a mouth but no anus, and rings of complex spines around its mouth.”



The findings make important amendments to the early phylogenetic tree and the understanding of how life developed. The story of Saccorhytus’ ancestry lies in the microscopic internal and external features of this tiny fossil.&nbsp;



By taking hundreds of X-ray images, the experts reconstructed a detailed 3D digital model of the fossil. This revealed that pores around the mouth were closed by another layer, creating spines around the mouth.



&nbsp;“We believe these would have helped Saccorhytus capture and process its prey,” said study co-author Huaqiao Zhang from the Nanjing Institute of Geology and Palaeontology.



The researchers believe that Saccorhytus is in fact an ecdysoszoan: a group that contains arthropods and nematodes.&nbsp;



“We considered lots of alternative groups that Saccorhytus might be related to, including the corals, anemones and jellyfish which also have a mouth but no anus,” said study co-lead author Professor Philip Donoghue of <a href="https://www.bristol.ac.uk/">University of Bristol</a>.



Saccorhytus’ lack of anus is an intriguing and important feature for a fundamental reason of evolutionary biology. How the anus arose – and sometimes subsequently disappeared – contributes to the understanding of how animal body plans evolved. Moving Saccorhytus to the ecdysozoan group means striking the feature of a disappearing anus off the deuterosome case history, and adding it to the ecdysozoan one.



“This is a really unexpected result because the arthropod group have a through-gut, extending from mouth to anus. Saccorhytus’s membership of the group indicates that it has regressed in evolutionary terms, dispensing with the anus its ancestors would have inherited,” said Shuhai Xiao from Virgina Tech. “We still don’t know the precise position of Saccorhytus within the tree of life but it may reflect the ancestral condition from which all members of this diverse group evolved.”



---



By <a href="mailto:katherinebucko@gmail.com">Katherine Bucko</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Mysterious creature with no anus is not a human ancestor

Researchers have discovered that a mysterious microscopic creature - from...

The location of continental plates affects how the ocean moves oxygen around. Continental movement could have the opposite effect, choking out marine oxygen killing most deep ocean creatures. These are the findings of a new study on oceanic oxygen.



“Continental drift seems so slow, like nothing drastic could come from it, but when the ocean is primed, even a seemingly tiny event could trigger the widespread death of marine life,” said study co-author Andy Ridgwell, a geologist at <a href="https://www.ucr.edu/">UC Riverside</a>.



The <a href="https://www.earth.com/news/snailfish-have-a-secret-weapon-to-survive-in-frozen-arctic-waters/">water</a> at the ocean’s surface becomes colder and denser as it approaches the north or south pole, and then it sinks. As the water sinks, it transports oxygen from Earth’s atmosphere down to the ocean floor.&nbsp;



Eventually, a return flow brings nutrients released from sunken organic matter back to the ocean’s surface, fuelling the growth of plankton. This function supports the incredible diversity of fish and other animals in today’s ocean.



For the study, the researchers investigated whether the location of continental plates affect how the ocean moves oxygen around. To their surprise, it does.&nbsp;



“Many millions of years ago, not so long after animal life in the ocean got started, the entire global ocean circulation seemed to periodically shut down,” said Ridgwell. “We were not expecting to find that the movement of continents could cause surface waters and oxygen to stop sinking, and possibly dramatically affecting the way life evolved on Earth.”



“Scientists previously assumed that changing oxygen levels in the ocean mostly reflected similar fluctuations in the atmosphere,” said study first author Alexandre Pohl.



The results show that collapse in global water circulation leads to a separation between oxygen levels in the upper and lower depths. For tens of millions of years, that separation caused the entire ocean seafloor to lose oxygen. This changed 440 million years ago at the start of the Silurian period.



“Circulation collapse would have been a death sentence for anything that could not swim closer to the surface and the life-giving oxygen still present in the atmosphere,” said Ridgwell. Creatures of the deep include bizarre-looking fish, giant worms and crustaceans, squid, sponges and more.



It is unknown whether the Earth could experience a similar event in the future. Existing climate models confirm that increasing global warming will weaken ocean circulation, and some models predict an eventual collapse of the branch of circulation that starts in the North Atlantic.“We’d need a higher resolution climate model to predict a mass extinction event,” said Ridgwell.&nbsp;



In theory, an unusually warm summer or the erosion of a cliff could trigger a cascade of processes that upends life as it appears today.&nbsp;



“You’d think the surface of the ocean, the bit you might surf or sail on, is where all the action is. But underneath, the ocean is tirelessly working away, providing vital oxygen to animals in the dark depths,” explained Ridgwell.&nbsp;



“The ocean allows life to flourish, but it can take that life away again. Nothing rules that out as continental plates continue to move.”



The study is published in the journal <a href="https://www.nature.com/articles/s41586-022-05018-z">Nature</a>.&nbsp;



---



By <a href="mailto:nire518@gmail.com">Erin Moody </a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

"Sleeping giant" could choke out oxygen on the ocean floor

The location of continental plates affects how the ocean moves...

Great,White,Sharks,By,Watersurface,View,From,Bottom

By using sophisticated electronic tags, a team of researchers led by <a href="https://www.stanford.edu/">Stanford University</a> has assembled a large biologging dataset to better understand how elasmobranchs – a group of marine animals including <a href="https://www.earth.com/news/sharks-important-deserve-protections/">sharks</a>, rays, and skates – use the ocean depths.&nbsp;



The analysis revealed that, while some species spend their entire lives in shallow waters close to the shores, others plunge hundreds of meters under water. Clarifying how elasmobranchs use the ocean will enable resource managers and policymakers to examine the threats these animals face, and devise better future management and conservation plans.



The researchers compiled two decades of satellite data and archival tags to track the movements of 38 species of elasmobranchs in oceans across the globe.&nbsp;



“For the first time, we have a standardized, global database that we used to fill important knowledge gaps about the diving behaviors of sharks and rays,” said study co-lead author Samantha Andrzejaczek, a postdoctoral fellow in Marine Biology at Stanford. “This will enable better understanding of what fisheries interact with elasmobranchs and how to improve management of many of these long-lived animals.”



According to the scientists, one of the most common movements among elasmobranchs appears to match up with the ocean’s diel (twice per day) vertical migration. At dawn, small fish and invertebrates begin migrating from the ocean’s surface to the safety of darker, deeper waters, where they are followed by their predators. At night, they swim back to the surface to feed.&nbsp;



“We think that sharks and rays in their diel migrations are following food resources up and down the water column,” reported Dr. Andrzejaczek. &nbsp;



About one-third of elasmobranch species frequently dive to deep water. For instance, white sharks (Carcharodon carcharias) were found to dive deeper than 1,200 meters, while whale sharks (Rhincodon typus) have reached a staggering 1,896 meters-deep.&nbsp;



“Deep divers might be looking for food in deeper water or avoiding hunters themselves as potential prey,” said Dr. Andrzejaczek. “Some sharks and rays are small, and some of the biggest sharks and rays will feed on them. We found that 13 species had individuals that dive to more than 1,000 meters, which is extremely deep.”&nbsp;Some of these animals may dive into the depths not only in search of prey, but also to cool down after spending too much time in the warm surface waters.



The scientists also identified overlaps among species in the same vertical spaces, mainly driven by predator-prey dynamics. For example, the oceanic manta ray and whale shark both feed on plankton, and the tiger shark is known to predate on both of these species.



These findings could help elasmobranch conservation efforts by identifying areas where they might be at risk of bycatch or other hazards.&nbsp;



“Human beings are unaccustomed to thinking of habitat in the vertical dimension. We hope this study can make people realize that we need management strategies that incorporate this overlooked dimension of elasmobranch behavior. For example, we could use these data to better understand how sharks and human fisheries interact,” Dr. Andrzejaczek concluded.



The study is published in the journal <a href="http://dx.doi.org/10.1126/sciadv.abo1754">Science Advances</a>.



---



By <a href="mailto:andrei.ionescu5891@gmail.com">Andrei Ionescu</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer&nbsp;&nbsp;

Scientists reveal how sharks use the oceans

By using sophisticated electronic tags, a team of researchers led...

The largest mass extinction in Earth's history marked the end of the Permian period, some 252 million years ago. Over 80 percent of all species around at the time disappeared forever from the fossil record. This changed the nature of life on <a href="https://www.earth.com/news/first-fruit-eating-animal-in-earths-history-identified/">Earth</a> and ushered in a new era in which the reptiles evolved and proliferated. In the past, biologists have understood that this rapid radiation of reptiles was driven by the plethora of ecological niches made available by the extinction of Permian species, but new research has now proposed that climate change was also a significant factor behind the spectacular evolution and expansion of reptiles at this time.&nbsp;



“We found that these periods of rapid evolution of reptiles were intimately connected to increasing temperatures. Some groups changed really fast and some less fast, but nearly all reptiles were evolving much faster than they ever had before,” said lead author Tiago R Simões, postdoctoral fellow at the Museum of Comparative Zoology and Department of Organismic and Evolutionary Biology, <a href="https://www.harvard.edu/">Harvard University</a>.



For the investigation, Simões and senior author Professor Stephanie E. Pierce (also from Harvard) worked alongside collaborators Professor Michael Caldwell (University of Alberta, Canada) and Dr. Christian Kammerer (North Carolina Museum of Natural Sciences) to examine early amniotes. These animals represent the forerunners of all modern mammals, reptiles, birds, and their closest extinct relatives, at the initial phase of their evolution. At this point in time, the first groups of reptiles and mammal ancestors were splitting from each other and evolving along their own separate evolutionary paths.



“Reptiles represent an ideal and rare terrestrial system to study this question as they have a relatively good fossil record and survived a series of climatic crises including the ones leading up to the largest extinction in the history of complex life, the Permian-Triassic mass extinction,” said Simões.



During the Permian period, it was the synapsids that dominated the vertebrate fauna. These were not reptiles, but the ancestors of mammals, known as stem mammals or proto-mammals. Most of them perished during the end Permian extinction, their ecological niches being taken over by reptiles, including numerous dinosaur species, that evolved and radiated rapidly during the Triassic Period (252-200 million years ago).



The new study, published in the journal <a href="https://www.science.org/journal/sciadv">Science Advances</a>, makes use of morphological data from more than 1,000 fossil specimens from 125 species of reptiles, synapsids, and their closest relatives during approximately 140 million years before and after the Permian-Triassic extinction. This data set is 40 percent larger than the previous largest data set and most of the measurements were made by direct observations and micro-CT scans.&nbsp;



The researchers analyzed this data to identify when these fossil species first originated and how fast they were evolving, using state-of-the-art analytical techniques such as Bayesian evolutionary analysis, which is also used to understand the evolution of viruses such as SARS-COVID 19. They then combined the morphological data with information on body size and with global temperature data that spanned millions of years in the geological record, to provide a broad overview of the animals’ major adaptive responses towards climatic shifts.



The experts found that the appearance of new species, increases in the rates of morphological change and alterations in geographical distributions corresponded to periods of rapidly changing climatic conditions, including global warming and cooling,



“Our results reveal that periods of fast climatic shifts and global warming are associated with exceptionally high rates of anatomical change in most groups of reptiles as they adapted to new environmental conditions, and this process started long before the Permian-Triassic extinction, since at least 270 million years ago, indicating that the diversification of reptile body plans was not triggered by the P-T extinction event as previously thought, but in fact started tens of million years before that," said Professor Pierce.



“One reptile lineage, the lepidosaurs, which gave rise to the first lizards and tuataras, veered in the opposite direction of most reptile groups and underwent a phase of very slow rates of change to their overall anatomy,” said Simões, “essentially, their body plans were constrained by natural selection, instead of going rogue and radically changing like most other reptiles at the time.” The researchers suggest this is due to pre-adaptations on their body size to cope better with high temperatures.



“The physiology of organisms is really dependent on their body size. Small-bodied reptiles can better exchange heat with their surrounding environment. The first lizards and tuataras were much smaller than other groups of reptiles, not that different from their modern relatives, and so they were better adapted to cope with drastic temperature changes. The much larger ancestors of crocodiles, turtles, and dinosaurs could not lose heat as easily and had to quickly change their bodies in order to adapt to the new environmental conditions.”



According to Professor Pierce, large-sized reptiles basically took two routes to deal with these climate shifts - they either migrated closer to temperate regions or invaded the aquatic world where they didn’t need to worry about overheating because water can absorb heat and maintain its temperature much better than air.



“This strong association between rising temperatures in the geological past and a biological response by dramatically different groups of reptiles suggests climate change was a key factor in explaining the origin and the explosion of new reptile body plans during the latest Permian and Triassic,” said Simões.



“We show that the origin and phenotypic radiation of reptiles was not solely driven by ecological opportunity following the end-Permian extinction, as previously thought, but was also the result of multiple adaptive responses to climatic shifts spanning 57 million years," concluded the study authors.&nbsp;



---



By <a href="mailto:bosman@truewan.co.za">Alison Bosman</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Past climate change drove the rapid evolution of reptiles

The largest mass extinction in Earth's history marked the end...

Small mammals will have a hard time surviving the stressors associated with climate change, according to a new study from the <a href="https://www.sdu.dk/en">University of Southern Denmark</a>. The experts found that large, long-lived animals are better able to cope with extreme weather such as prolonged <a href="https://www.earth.com/news/europe-is-experiencing-its-worst-drought-in-500-years/">drought</a> and heavy rainfall.



The researchers analyzed historical population fluctuations among 157 mammal species from around the world. These fluctuations were compared with weather and climate data from the same time period.&nbsp;



The results are providing new insight into how animals respond to extreme weather. In particular, the experts have identified which animal populations will be the hardest hit by climate change.



"We can see a clear pattern: Animals that live a long time and have few offspring are less vulnerable when extreme weather hits than animals that live for a short time and have many offspring," said study co-author Professor Owen Jones.



Large animals that live longer can cope better with an extreme event such as a persistent drought because these animals have the option to wait until conditions improve to reproduce. The same weather event would affect small mammals differently, as food sources like insects, flowers, and fruits would disappear quickly.&nbsp;



On the other hand, populations of small mammals may also take advantage when weather conditions improve by producing many offspring.



"These small mammals react quickly to extreme weather, and it goes both ways. Their vulnerability to extreme weather should therefore not be equated with a risk of extinction," said study co-author John Jackson.&nbsp;



Some of the animals that will be the most affected by climate change include: Azara's grass mouse, olive grass mouse, elegant fat-tailed mouse opossum, Canadian lemming, Tundra vole, Arctic fox, and the common shrew.



Meanwhile, larger-bodied animals such as African elephants, Siberian tigers, chimpanzees, greater horseshoe bats, llamas, and grizzly bears will be less impacted by extreme weather conditions.&nbsp;



According to the researchers, the results of the study may help experts make predictions about animals they do not know much about.&nbsp;



"We expect climate change to bring more extreme weather in the future. Animals will need to cope with this extreme weather as they always have. So, our analysis helps predict how different animal species might respond to future climate change based on their general characteristics – even if we have limited data on their populations," said Professor Jones.



Jackson emphasized that the ability of an animal species to withstand climate change is not the only factor to consider when assessing the species’ vulnerability to extinction:



"Habitat destruction, poaching, pollution and invasive species are factors that threaten many animal species - in many cases even more than climate change," said Jackson.&nbsp;



The study is published in the journal <a href="https://elifesciences.org/">eLife</a>.



---



By <a href="http://csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Which animals are most affected by extreme weather?

Small mammals will have a hard time surviving the stressors...

A humble shrimp is raising an alarm about climate change. A study published in the journal <a href="https://www.frontiersin.org/articles/10.3389/fmars.2022.960881/full?&amp;utm_source=Email_to_authors_&amp;utm_medium=Email&amp;utm_content=T1_11.5e1_author&amp;utm_campaign=Email_publication&amp;field=&amp;journalName=Frontiers_in_Marine_Science&amp;id=960881">Frontiers in Marine Science</a> has verified <a href="https://www.whoi.edu/press-room/news-release/warming-oceans-are-getting-louder/">previous observations</a> that two species of snapping shrimp snap louder and more frequently in warmer water.&nbsp;



Scientists from <a href="https://www.whoi.edu/">Woods Hole Oceanographic Institution</a> (WHOI), Ashlee Lillis and T. Aran Mooney, were able to draw a clear connection between warming and snapping by analyzing shrimp off the coast of North Carolina.&nbsp;



The researchers observed that for every one degree (C) increase in water temperature, the shrimp snapped one to two decibels higher and increased in frequency by 15 to 60 percent. The researchers also discovered that the frequency of snaps more than doubled when the water was between 68 and 86 degrees Fahrenheit.



This behavior change is important because these tiny shrimp have a tremendous influence on the environment. Whales and dolphins use their sounds to navigate coastal areas, and the snapping attracts fish, shellfish, and coral larvae to good settling areas.



"These shrimp are the most ubiquitous sound producer in the ocean, and now we have evidence that temperature has a huge impact on their behavior and the overall soundscape," said Lillis, principal scientist at Sound Ocean Science. "That's relevant to everything from migrating whales to larvae trying to use the soundscape, or humans who use the sea for extractive or military purposes."



Mooney points out that although it's crucial for functioning ocean systems, crustacean behavior - as it affects the larger ecosystem - is often ignored when considering the consequences of climate change.&nbsp;



The research was conducted during a short-term heatwave, and the study authors stress that there are still many unanswered questions.&nbsp;



"Climate change is impacting the marine soundscape in fundamental ways," Mooney said. "Warming waters can influence how animals are physically able to communicate and use sound to reproduce and attract mates. We don't yet know what happens to the ecosystem when background noise levels are higher, but there are far-reaching implications."



---



By <a href="mailto:nire518@gmail.com">Erin Moody </a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Snapping shrimp are getting louder as the ocean warms

A humble shrimp is raising an alarm about climate change....

The mountains of the Philippines are a biodiversity hotspot - home to more unique species of mammals than anywhere else on Earth. Filipino biologist Danilo Balete has spent most of his adult life doing fieldwork and recording the fascinating diversity of living creatures in these mountains. One of the mice he discovered has recently been revealed to belong not only to a new species, but to a whole new genus of rodents.&nbsp;



Larry Heaney, curator of mammals at Chicago’s <a href="https://www.fieldmuseum.org/">Field Museum</a> is the senior author of a paper describing the new mouse.in the&nbsp;<a href="https://academic.oup.com/jmammal">Journal of Mammalogy</a>. “In the past several decades, we’ve learned just how incredibly important the Philippines are in terms of being home to mammals that are found nowhere else," said Heaney, "and a lot of that knowledge can be traced back to fieldwork led by Danny Balete."



Before his untimely death in 2017, Danny Balete’s research overturned previously held notions that biodiversity decreases in mountainous regions because of their harsh environmental conditions. Instead, he proposed that mountainous environments could generate, rather than suppress, species diversity. The mountains of the Philippines are cooler and much wetter than surrounding lowlands, so they become like islands, isolated within the lowland environment below.&nbsp;



Fauna and flora on these “sky islands” tend to evolve separately from each other, meaning that each mountain or mountain range may end up with new and unique species. “The taller and the bigger the mountain range, the more species of mammals will be living there that don't live anywhere else in the world,” said Heaney, who has been studying the mammals of the Philippines for 40 years. He first met Danny Balete in the late 1980s, shortly after Danny completed his Bachelor’s degree at the University of the Philippines.



"I was establishing a research program, and asked around, ‘Who would be a really good, enthusiastic young person to take into the field?’ And several people immediately said, ‘Danny Balete.’ So I invited him to do some field work with me, and he did fantastically well,” recalls Heaney. “He was just a superb field biologist. Danny could identify every plant, every frog, every bug, everything that you encountered, it was just astounding.”



“Danny contributed hugely to scientific knowledge about biological diversity in the Philippines. His enjoyment of biodiversity was really infectious, making him a mentor and inspiration to a generation of researchers and conservationists,” said study co-author Professor Mariano Roy Duya.."By the time of his death, at far too young an age, he was already one of the most prominent biodiversity scientists working in the Philippines.”



In 2007 and 2010, Balete went on expeditions to Mount Kampalili on the island of Mindanao as part of a Field Museum collaboration with the Philippine Eagle Foundation. They wanted to know what mammals lived alongside one of the largest and most critically endangered birds, the Philippine Eagle, and Danny was the perfect person to take along. While on Mount Kampalili, he and the team made a startling discovery: a dark brown mouse with small eyes and a long, tapering nose like a shrew. The creature was different from anything he’d ever seen on that island and looked more like mice he’d seen before, hundreds of miles away, on the island of Luzon.



“High up in the mountains, Danny was able to get cell phone service, so he sent me a text message right away, saying, ‘We just caught this animal that looks a lot like the ones from Luzon and it shouldn’t be here,’” recalls Heaney. “So he immediately recognized that this was something really cool.”



DNA analysis was conducted on three specimens of the new mouse by Dakota Rowsey, the study’s first author, vertebrate collections manager at Arizona State University, and research associate at the Field Museum. The results confirmed that the rodent was different from any known to science, to the extent that it represents a brand new genus of mice. The researchers decided to name the new species Baletemys kampalili, in honor of their departed colleague.&nbsp;



“That DNA study demonstrated that the new mouse was not related to the species up in the northern Philippines, but instead was related to species from Mindanao.&nbsp; It appears to be a remarkable case of what biologists call convergence – distantly related species that have independently evolved to resemble each other in ways that allow them to use habitats and resources in similar ways,” said Rowsey.



“Naming a new species after anyone is a big deal, a major honor given to people who make long-term, high-impact contributions to biodiversity science. Naming a new genus after someone is one of the highest honors biologists can bestow.”



It is not uncommon to discover new species, but a whole new genus is something special. “New species of mammals are being discovered globally at a considerable clip, maybe 50 to 100 new species per year,” said Heaney. “Finding a brand-new genus, previously unknown to science like this one, that only happens at most a couple of times per year. In our 40 years of intensive study of Philippine mammals, this is one of nearly 50 new species, but just the fourth new genus we discovered.”



The new genus’s scientific name means “Balete’s mouse,” in honor of Balete’s work in discovering it and so many other creatures. “As we began picking up the pieces after his death, it became obvious to us that we had to name this new mouse after him; he deserves this,” said Professor Duya.



In addition to honoring Balete, the researchers say the new genus is important because it’s another puzzle piece in understanding the diversity of life in the Philippines. Demonstrating that Mount Kampalili is home to a mouse found nowhere else on Earth may bolster conservation efforts by Indigenous communities which would help the mouse’s neighbors, including the critically endangered Philippine Eagles.



“It’s really important to show that when we protect one species, like the magnificent Philippine Eagle, we protect not only our unique biological wealth but our cultural heritage as well,” said study co-author Jayson Ibanez of the Philippine Eagle Foundation.



The Philippine eagle and the new “Balete’s mouse” are neighbors to the Indigenous Mandaya group&nbsp;of Mount Kampalili. “Indigenous peoples get very excited whenever they learn that they share their homeland with a totally unique lifeform. And in this case, when we help protect Mount Kampalili, we also protect the primary watershed, airsheds, and biocultural sanctuaries for much of southeastern Mindanao, giving huge benefits to all the people who live here,” said Ibanez. “With all of the threats from watershed destruction and climate change, we need all the help we can get.”



---



By <a href="mailto:bosman@truewan.co.za">Alison Bosman</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Shrew-like mouse will help protect Phillipine eagles

The mountains of the Philippines are a biodiversity hotspot -...

Hubendickia lancangensis

Taxonomic tree: