Tuesday, August 24, 2021

The science of ants' underground cities


Peer-Reviewed Publication

CALIFORNIA INSTITUTE OF TECHNOLOGY

Picture an anthill. What do you see? A small mound of sand and crumbly dirt poking up through the lawn? A tiny hole disappearing into the ground? A few ants scrambling around busily. Not very impressive, right? 

But slip beneath the surface and the above-ground simplicity gives way to subterranean complexity. Tunnels dive downward, branching and leading to specialized chambers that serve as home for the colony's queen, as nurseries for its young, as farms for fungus cultivated for food, and as dumps for its trash. These are not just burrows. They are underground cities, some of them home to millions of individuals, reaching as far as 25 feet underground, often lasting for decades. 

This kind of construction would be an impressive undertaking for most creatures, but when performed by animals that don't get much bigger than your fingernail, it is especially remarkable. 

Now, driven by the desire to improve our own ability to dig underground—whether it is for mining, subways or underground farming—a team of researchers from Caltech has unraveled one of the secrets behind how ants build these amazingly complex and stable structures. 

Led by the laboratory of Jose Andrade, the George W. Housner Professor of Civil and Mechanical Engineering, the team studied the digging habits of ants and uncovered the mechanisms guiding them. The research is described in a paper published in the journal Proceedings of the National Academy of Sciences.

What are ants thinking (if anything)?

Before beginning this research, Andrade, who is also the Cecil and Sally Drinkward Leadership Chair and Executive Officer for Mechanical and Civil Engineering, had a big question he wanted to answer: Do ants "know" how to dig tunnels, or are they just blindly digging?

"I got inspired by these exhumed ant nests where they pour plastic or molten metal into them and you see these vast tunnel systems that are incredibly impressive," Andrade says. "I saw a picture of one of these next to a person and I thought 'My goodness, what a fantastic structure.' And I got to wondering if ants 'know' how to dig."

"We didn’t interview any ants to ask if they know what they're doing, but we did start with the hypothesis that they dig in a deliberate way," Andrade says. "We hypothesized that maybe ants were playing Jenga."

What he means by "playing Jenga" is that the team suspected the ants were feeling their way around in the dirt, looking for loose grains of soil to remove, in much the same way a person playing Jenga checks for loose blocks that are safe to take out of the stack. The blocks that can't be removed—the ones bearing the load of the stack—are said to be part of the structure's 'force chains,' the collection of pieces jammed together by the forces placed on them. 

"We hypothesized that the ants could sense these force chains and avoided digging there," Andrade says. "We thought maybe they were tapping grains of soil, and that way they could assess the mechanical forces on them."

Ants do what they want

To learn about ants, the team needed to have ants to study. But Andrade is an engineer, not an entomologist (someone who studies insects), so he enlisted the help of Joe Parker, assistant professor of biology and biological engineering, whose research focuses on ants and their ecological relationships with other species. 

"What Jose and his team needed was somebody who works with ants and understands the adaptive, collective behaviors of these social insects to give them some context for what they were doing," Parker says. 

With Parker on board, the team started culturing ants and learning how to work with them. It was a process that took nearly a year, Andrade says. Not only did they need to breed enough ants to work with, there was a lot of trial and error involved in getting the ants to dig in little cups of soil that they could load into an X-ray imager. Through that work, they determined an optimal size of cup to use, and an ideal number of ants to put in each cup. Still, the ants did not always cooperate with the researchers' own priorities. 

"They're sort of capricious," Andrade says. "They dig whenever they want to. We would put these ants in a container, and some would start digging right away, and they would make this amazing progress. But others, it would be hours and they wouldn’t dig at all. And some would dig for a while and then would stop and take a break." 

But once the ants got going, the researchers would take the little cups and X-ray them using a technique that created a 3-D scan of all the tunnels inside. By taking a series of these scans, letting the ants work a little bit between each, the researchers could create simulations showing the progress the ants made as they extended their tunnels further and further below the surface. 

The caterpillar is protected by “Kropotkin” ants – Small Meat Ant Iridomyrmex sp. The ants provide protection in return for sugary fluids secreted by caterpillar. Imperial Hairstreaks will only return to breed where both caterpillar food plants and the ants are present. Kropotkin is a reference to Russian biologist Peter Kropotkin who proposed a concept of evolution based on “mutual aid” between species helping species from ants to higher mammals survive.

Understanding ant physics

Next, Andrade's team set about analyzing what the ants were actually doing as they worked, and a few patterns emerged. For one, Andrade says, the ants tried to be efficient as possible. That meant they dug their tunnels along the inside edges of the cups, because the cup itself would act as part of their tunnels' structures, resulting in less work for them. They also dug their tunnels as straight as possible. 

"That makes sense because a straight line is the shortest path between two points," Andrade says. "And with them taking advantage of the sides of the container, it shows that the ants are very efficient at what they do."

The ants also dug their tunnels as steeply as they possibly could, right up to what's known as the angle of repose. That angle represents the steepest angle that a granular material—a material made of individual grains—can be piled up before it collapses. To understand the angle of repose, picture a child building a sand castle at the beach. If the child uses dry sand, every scoop of sand they add will slide down the sides of the pile they've already made. More sand will make the pile taller, but also wider, and it will never get steeper. On the other hand, if the child uses wet sand, they will be able to pile the sand steeply enough to build walls, and towers, and all the other things a sand castle might have. Wet sand has a higher angle of repose than dry sand, and every granular material has an angle that is unique to it. The ants, Andrade says, can tell how steep that angle is for whatever they're digging in, and they don't exceed it. That, too, makes sense, he says.

"If I'm a digger, and I'm going to survive, my digging technique is going to align with the laws of physics, otherwise my tunnels are going to collapse and I'm going to die," he says. 

Finally, the team discovered something about the physics of ant tunnels that could one day be useful to humans. 

As ants remove grains of soil they are subtly causing a rearrangement in the force chains around the tunnel. Those chains, somewhat randomized before the ants begin digging, rearrange themselves around the outside of the tunnel, sort of like a cocoon or liner. As they do so, two things happen: 1.) the force chains strengthen the existing walls of the tunnel and 2.) the force chains relieve pressure from the grains at end of the tunnel where the ants are working, making it easier for the ants to safely remove them. 

"It's been a mystery in both engineering and in ant ecology how ants build these structures that persist for decades," Parker says. "It turns out that by removing grains in this pattern that we observed, the ants benefit from these circumferential force chains as they dig down." 

But what about the central question of the team's hypothesis? Are ants aware of what they're doing when they dig?

What ants know and don't

"What we discovered was that they didn’t seem to 'know' what they are doing," Andrade says. "They didn’t systematically look for soft spots in the sand. Rather, they evolved to dig according to the laws of physics."

Parker calls this a behavioral algorithm. 

"That algorithm does not exist within a single ant," he says. "It's this emergent colony behavior of all these workers acting like a superorganism. How that behavioral program is spread across the tiny brains of all these ants is a wonder of the natural world we have no explanation for."

Andrade says he hopes to begin working on an artificial intelligence approach that can emulate that behavioral algorithm so he can simulate how ants dig on a computer. Part of that emulation, Andrade says, will be determining how to scale ant physics for human-sized tunnels. 

"Granular materials scale in different ways than other materials like fluids or solids," he says. "You can go from experiments at the grain scale, in this case a few millimeters, to the meter scale, by scaling the intergranular friction coefficient."

The next step after that? Robotic ants that could dig tunnels for humans. 

"Moving granular materials is very energy intensive, and it's very expensive and you always need an operator there running the machines," he says. "This would be the final frontier."

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The paper describing the research, titled, "Unearthing real time 3D ant tunneling mechanics," appears in the August 23 issue of the journal Proceedings of the National Academy of Sciences.

Co-authors are Robert Buarque de Macedo, applied mechanics graduate student; Shilpa Joya, a former PhD student at Caltech; Edward Andò and Gioacchino Viggiani of Université Grenoble Alpes; and Raj Kumar Pal of Kansas State University.

Funding for the research was provided by a grant from the United States Army Research Office.

  




 

Statistics say large pandemics are more likely than we thought


Most people are likely to experience an extreme pandemic like COVID-19 in their lifetime

Peer-Reviewed Publication

DUKE UNIVERSITY

DURHAM, N.C. -- The COVID-19 pandemic may be the deadliest viral outbreak the world has seen in more than a century. But statistically, such extreme events aren’t as rare as we may think, asserts a new analysis of novel disease outbreaks over the past 400 years.

The study, appearing the week of Aug. 23 in the Proceedings of the National Academy of Sciences, used a newly assembled record of past outbreaks to estimate the intensity of those events and the yearly probability of them recurring.

It found the probability of a pandemic with similar impact to COVID-19 is about 2% in any year, meaning that someone born in the year 2000 would have about a 38% chance of experiencing one by now. And that probability is only growing, which the authors say highlights the need to adjust perceptions of pandemic risks and expectations for preparedness.

“The most important takeaway is that large pandemics like COVID-19 and the Spanish flu are relatively likely,” said William Pan, Ph.D., associate professor of global environmental health at Duke and one of the paper’s co-authors. Understanding that pandemics aren’t so rare should raise the priority of efforts to prevent and control them in the future, he said.     

The study, led by Marco Marani, Ph.D., of the University of Padua in Italy, used new statistical methods to measure the scale and frequency of disease outbreaks for which there was no immediate medical intervention over the past four centuries. Their analysis, which covered a murderer’s row of pathogens including plague, smallpox, cholera, typhus and novel influenza viruses, found considerable variability in the rate at which pandemics have occurred in the past. But they also identified patterns that allowed them to describe the probabilities of similar-scale events happening again.    

In the case of the deadliest pandemic in modern history – the Spanish flu, which killed more than 30 million people between 1918 and 1920 -- the probability of a pandemic of similar magnitude occurring ranged from 0.3% to 1.9% per year over the time period studied. Taken another way, those figures mean it is statistically likely that a pandemic of such extreme scale would occur within the next 400 years.    

But the data also show the risk of intense outbreaks is growing rapidly. Based on the increasing rate at which novel pathogens such as SARS-CoV-2 have broken loose in human populations in the past 50 years, the study estimates that the probability of novel disease outbreaks will likely grow three-fold in the next few decades.        

Using this increased risk factor, the researchers estimate that a pandemic similar in scale to COVID-19 is likely within a span of 59 years, a result they write is “much lower than intuitively expected.” Although not included in the PNAS paper, they also calculated the probability of a pandemic capable of eliminating all human life, finding it statistically likely within the next 12,000 years.       

That is not to say we can count on a 59-year reprieve from a COVID-like pandemic, nor that we’re off the hook for a calamity on the scale of the Spanish flu for another 300 years. Such events are equally probable in any year during the span, said Gabriel Katul, Ph.D., the Theodore S. Coile Distinguished Professor of Hydrology and Micrometeorology at Duke and another of the paper’s authors.       

“When a 100-year flood occurs today, one may erroneously presume that one can afford to wait another 100 years before experiencing another such event,” Katul says. “This impression is false. One can get another 100-year flood the next year.”    

As an environmental health scientist, Pan can speculate on the reasons outbreaks are becoming more frequent, noting that population growth, changes in food systems, environmental degradation and more frequent contact between humans and disease-harboring animals all may be significant factors. He emphasizes the statistical analysis sought only to characterize the risks, not to explain what is driving them.          

But at the same time, he hopes the study will spark deeper exploration of the factors that may be making devastating pandemics more likely – and how to counteract them.         

“This points to the importance of early response to disease outbreaks and building capacity for pandemic surveillance at the local and global scales, as well as for setting a research agenda for understanding why large outbreaks are becoming more common,” Pan said.

Marani, the paper’s lead author, holds an adjunct appointment at Duke, where he previously was a professor of civil and environmental engineering. Another co-author, Anthony Parolari, Ph.D., of Marquette University, is a former Duke postdoctoral researcher.

CITATION: “Intensity and Frequency of Extreme Novel Pandemics,” Marco Marani, Gabriel Katul, William Pan and Anthony Parolari. Proceedings of the National Academy of Sciences, Aug. 23, 2021. DOI: 10.1073/pnas.2105482118

 

On the “Island of the Blue Dolphins,” a glimmer of hope for a rare fox species


Peer-Reviewed Publication

ECOLOGICAL SOCIETY OF AMERICA

San Nicolas Island drought 

IMAGE: A VIEW OF DROUGHT-AFFECTED HABITAT ON SAN NICOLAS ISLAND, INCLUDING LARGE PATCHES OF DEAD ICE PLANT, A ONCE-FAVORED FOOD OF ISLAND FOXES, IN THE FOREGROUND. view more 

CREDIT: FRANCESCA FERRARA / U.S. NAVY

The San Nicolas Island fox, a subspecies of the Channel Island Fox only found on the most remote of California’s eight Channel Islands, is at a low risk of extinction, new research published last week in Ecosphere shows.  

In the past decade, the population of San Nicolas Island fox has decreased by nearly half, with just 332 foxes remaining in 2016.

The study, conducted by researchers from Montana State University, the University of Colorado and Naval Base Ventura County, predicted future fox population sizes assuming that current relatively dry environmental conditions persist. The foxes went extinct within 50 years in only 2.5% of the computer model’s simulations.

“This relatively low extinction risk is good news for San Nicolas Island foxes, but they are not out of the woods,” said Victoria Bakker, an assistant research professor at Montana State University and the paper’s lead author. “As a top carnivore living on a small island with degraded and invaded habitats, they are likely to experience the effects of climate change earlier and more acutely than other species. If climate change leads to even more frequent or severe droughts, the risk to foxes could rise substantially.” 

The research points to strategies that could increase the foxes’ resilience to a changing climate and other human-caused shifts that have contributed to their decline.

According to co-author Francesca Ferrara, a natural resource specialist at Naval Base Ventura County, the island’s resource managers are focusing on biosecurity, restoration of habitat and food resources, and minimizing human-wildlife conflict.  

Biosecurity efforts in particular have been drawn into the spotlight over the past year.

“We have ongoing vaccination and monitoring programs in place to ensure that no new invasive species or pathogens establish themselves on the island,” said Ferrara. “As the world has now seen with the COVID-19 pandemic, a population that has not been previously exposed to a disease or pathogen can quickly be decimated by it. Due to their isolation, the island foxes are at risk to diseases that normally circulate in mainland wildlife. Since they have never been exposed and have no natural immunity, a pathogen that is mild to a mainland species could prove deadly to the island fox.”

San Nicolas Island is the setting for the popular 1960 children’s novel Island of the Blue Dolphins, which draws from the story of Juana Maria, a Native Islander woman who spent 18 years alone on the island after her people were removed in 1835.

Today, San Nicolas Island functions as a United States naval station, but according to Ferrara, the island has retained its sense of remoteness and distinctiveness.

“The island fox really has a special place in my heart,” Ferrara said. “They never cease to delight me. They are bold and curious; their attitude and spunkiness is unmatched. I feel so fortunate that I can not only regularly cross paths with a small island fox foraging for insects but then shortly afterwards I can head over to observe one of the largest active rookeries of thousands of enormous breeding northern elephant seals.”

The naval base’s environmental staff manages the island’s wildlife and natural resources in order to support Department of Defense mission readiness.

 San Nicolas Island fox 

CAPTION

A San Nicolas Island fox observing its habitat. Island foxes are one of the world's smallest canids, about the size of a housecat.

CREDIT

Francesca Ferrara / U.S. Navy


CAPTION

San Nicolas Island fox resting with pup. Pup numbers are highest following years of high rainfall.

CREDIT

Francesca Ferrara / U.S. Navy

Journal article:
Bakker V.J., Doak D.F., and Ferrara F.J. 2021. Understanding extinction risk and resilience in an extremely small population facing climate and ecosystem change. Ecosphere; doi.org/10.1002/ecs2.3724

Authors:
Victoria J. Bakker1, Daniel F. Doak2, and Francesca J. Ferrara3
1Department of Ecology, Montana State University, Bozeman, Montana; 2Department of Environmental Studies, University of Colorado, Boulder, Colorado; 3Naval Base Ventura County, Point Mugu, California

Author contact:
Victoria Bakker (moc.liamg@rekkabjv)

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The Ecological Society of America, founded in 1915, is the world’s largest community of professional ecologists and a trusted source of ecological knowledge, committed to advancing the understanding of life on Earth. The 9,000 member Society publishes five journals and a membership bulletin and broadly shares ecological information through policy, media outreach, and education initiatives. The Society’s Annual Meeting attracts 4,000 attendees and features the most recent advances in ecological science. Visit the ESA website at https://www.esa.org.

 

 San Nicolas Island coastline 

CAPTION

The rugged coastline of San Nicolas Island, the most remote of the California Channel Islands.

CREDIT

Francesca Ferrara / U.S. Navy

 

To understand future habitat needs for chimpanzees, look to the past


New study examines where chimpanzees found refuge from climate instability during the past 120,000 years

Peer-Reviewed Publication

WILDLIFE CONSERVATION SOCIETY

chimpanzee 

IMAGE: A NEW STUDY EXAMINES WHERE CHIMPANZEES FOUND REFUGE FROM CLIMATE INSTABILITY DURING THE PAST 120,000 YEARS view more 

CREDIT: EMMA STOKES/WCS

A new study provides insight into where chimpanzees (Pan troglodytes) avoided climate instability during glacial and interglacial periods in Africa over the past 120,000 years. Using bioclimatic variables and other data, the study identified previously unknown swaths of habitat, rich in figs and palms, where chimps rode out the changes seen since the Last Interglacial period.

The findings, published in the journal in the American Journal of Primatology, help to increase the understanding of how climate change impacts biodiversity, and how to mitigate against predicted biodiversity loss in the future. This research was led by the German Centre for Integrative Biodiversity Research (iDiv), the Max Planck Institute for Evolutionary Anthropology, and an international team of over 80 collaborators from research institutes across the globe.

For their analysis, the authors compiled over 130,000 occurrence records of chimpanzees stored in the A.P.E.S. database of the International Union for Conservation of Nature (IUCN) Species Survival Commission (SSC), as well as data from the Pan African Programme: The Cultured Chimpanzee (PanAf) at the MPI-EVA and iDiv, Leipzig (http://panafrican.eva.mpg.de/).

The researchers quantified chimpanzee habitat suitability using species distribution models based on chimpanzee occurrences, climate and human density data, and then projected these models onto temporal snapshots of climate reconstructions at up to 1000 year intervals, dating back to the Last Interglacial period (120,000 years ago). For the first time, they were able to build a dynamic model of habitat suitability over time, permitting long-term stability (i.e. glacial refugia) to be calculated.

Results show that glacial refugia across Africa may have been underestimated for chimpanzees, with potentially up to 60,000 additional square kilometers (23,166 square miles) in the Upper and Lower Guinea Forests in West and Central Africa, and the Albertine Rift in East Africa.

In addition, results provide explicit insights into chimpanzee habitat and how it may have shifted throughout time, enabling hypotheses of how global change has affected genetic and behavioral diversity to be tested in the future.

Said lead author of the study Chris Barratt, a postdoctoral researcher at iDiv: “By integrating past climate and human density estimates, as well as species richness of keystone tropical plants (figs and palms), this study provides strong evidence of glacial refugia for chimpanzees being geographically larger than previously thought. It may well be that some of these refugia deserve greater levels of protection than they currently receive as they are important for the persistence of populations and species during periods of global change.”

The results provide a new resource for understanding patterns of genetic and behavioral diversity in chimpanzees. Chimpanzees exhibit highly differentiated genetic diversity (for example, lower in West Africa and higher in East and Central Africa), as well as high levels of behavioral differentiation based on the environmental variability they are exposed to, including Pleistocene forest refugia.

Said Hjalmar Kühl at iDiv, and senior author of the study: “We are only beginning to understand how past environmental changes have influenced the diversity in great apes we find today. A better understanding of these processes will tell us when variable environments serve as engines of diversification and when not. In the end these insights into great apes will also offer insights into our own evolution.”

Said Fiona Maisels of the Wildlife Conservation Society and a co-author of the study: “To effectively conserve chimpanzees (and other species) over the centuries to come, it is essential to understand the past. Humans are changing the planet’s climate and its habitats ever more rapidly. Approaches such as those used in this study are vital for predicting how these changes will affect future wildlife abundance and distribution, and to ensure space and safety for a multitude of species.”

 

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WCS (Wildlife Conservation Society)

MISSION: WCS saves wildlife and wild places worldwide through science, conservation action, education, and inspiring people to value nature. To achieve our mission, WCS, based at the Bronx Zoo, harnesses the power of its Global Conservation Program in nearly 60 nations and in all the world’s oceans and its five wildlife parks in New York City, visited by 4 million people annually. WCS combines its expertise in the field, zoos, and aquarium to achieve its conservation mission. Visit: newsroom.wcs.org Follow: @WCSNewsroom. For more information: 347-840-1242.

 

 

Speedy evolution: Sustained fast rates of evolution explain how tetrapods evolved from fish

Speedy Evolution
The aerial scene depicts two Late Devonian early tetrapods - Ichthyostega and Acanthostega - coming out of the water to move on land. Footprints trail behind the animals to show a sense of movement. Credit: Davide Bonadonna

One of the biggest questions in evolution is when and how major groups of animals first evolved. The rise of tetrapods (all limbed vertebrates) from their fish relatives marks one of the most important evolutionary events in the history of life. This "fish-to-tetrapod" transition took place somewhere between the Middle and Late Devonian (~400-360 million years ago) and represents the onset of a major environmental shift, when vertebrates first walked onto land. Yet, some of the most fundamental questions regarding the dynamics of this transition have remained unresolved for decades.

In a study published August 23 in Nature Ecology and Evolution Harvard researchers establish the origin date of the earliest tetrapods and discover they acquired several of the major new adaptive traits that enabled vertebrate life on land at accelerated evolutionary rates.

The study led by Dr. Tiago R. Simões, postdoctoral researcher, and senior author Professor Stephanie E. Pierce, both from the Department of Organismic and Evolutionary Biology, Harvard University, applied recently developed  (Bayesian evolutionary analysis) to precisely estimate the time and rates of anatomical  during the rise of tetrapods. The Bayesian method was adapted from methods originally developed in epidemiology to study how viruses like COVID-19 evolve and only recently became a tool in paleontology for the study of species evolution.

The study also innovates by combining data from  and body fossils to pinpoint the time of origin of the tetrapods. "Normally footprint data shows up after body fossils of their track makers. In this case, we have  footprints much older than the first body fossils by several million years, which is extremely unusual. By combining both footprint and body fossils, we could search for a more precise age for the rise of tetrapods," said Pierce.

"We were able to provide a very precise age for the origin of tetrapods at approximately 390 million years ago, 15 million years older than the oldest tetrapod body fossil," said Simões.

The researchers also found that most of the close relatives to tetrapods had exceptionally slow rates of anatomical evolution, suggesting the fish relatives to tetrapods were quite well adapted to their aquatic lifestyle.

"On the other hand, we discovered the evolutionary lineages leading to the first tetrapods broke away from that stable pattern, acquiring several of the major new adaptive traits at incredibly fast rates that were sustained for approximately 30 million years," said Simões.

Speedy Evolution
Animal silhouette colors represent rates of anatomical evolution for different body regions whereas background colors indicate groups undergoing stabilizing vs directional evolution towards new body plans. Credit: Tiago R. Simões and Stephanie E. Pierce

Simões and Pierce also extended molecular approaches to study how fast different parts of the early tetrapod body plan evolved—such as the skull, jaws, and limbs—and the strength of natural selection acting on each of them. They found that all parts of the tetrapod skeleton were under strong directional selection to evolve new adaptive features, but that the skull and jaws were evolving faster than the rest of the body, including the limbs

"This suggest that changes in the skull had a stronger role in the initial stages of the fish-to-tetrapod transition than changes in the rest of the skeleton. The evolution of limbs to life on land was important, but mostly at a later stage in tetrapod evolution, when they became more terrestrial," said Pierce.

"We see several anatomical innovations in their skull related to feeding and food procurement, enabling a transition from a fish-like suction-based mode of prey capture to tetrapod-like biting, and an increase in orbit size and location" said Simões. "These changes prepared tetrapods to look for food on land and to explore new food resources not available to their fish relatives."

The researchers also found that the fast rates of anatomical evolution in the tetrapod lineage were not associated with fast rates of species diversification. In fact, there were very few species around, so few they had a very low probability of being preserved in the fossil record.

This finding helps to answer an ongoing debate in evolution of whether new major animal groups originated under fast rates of anatomical change and species diversification (the classical hypothesis). Or, if there were high rates of anatomical evolution first, with increased rates of species diversification occurring only several million years later (a new hypothesis).

"What we've been finding in the last couple of years is that you have lots of anatomical changes during the construction of new animal body plans at short periods of geological time, generating high rates of anatomical evolution, like we're seeing with the first tetrapods. But in terms of number of species, they remained constrained and at really low numbers for a really long time, and only after tens of millions of years do they actually diversify and become higher in number of species. There's definitely a decoupling there," said Simões.

Pierce agreed, "It takes time to get a foothold in a new niche in order to take full advantage of it."

"Our study starts at the very beginning of this evolutionary story. There are many, many more chapters to come," said Pierce. "We want to next dig further in terms of what happened after the origin of tetrapods, when they started to colonize land and diversify into new niches. How does that impact their anatomical rates of evolution compared to their species diversification across the planet? This is just the very beginning. It's the introductory chapter to the book."

Water-to-land transition in early tetrapods

More information: Sustained high rates of morphological evolution during the rise of tetrapods, Nature Ecology and Evolution (2021). DOI: 10.1038/s41559-021-01532-x , www.nature.com/articles/s41559-021-01532-x

Journal information: Nature Ecology & Evolution 

Provided by Harvard University 

 

Volcanoes acted as a safety valve for Earth's long-term climate

Volcanoes acted as a safety valve for Earth’s long-term climate
Continental volcanic arcs such as this one in Kamchatka, Russia, are rapidly weathered,
 driving CO2 removal from the atmosphere over geological time. 
Credit: Tom Gernon, University of Southampton

Scientists at the University of Southampton have discovered that extensive chains of volcanoes have been responsible for both emitting and then removing atmospheric carbon dioxide (CO2) over geological time. This stabilized temperatures at Earth's surface.

The researchers, working with colleagues at the University of Sydney, Australian National University (ANU), University of Ottawa and University of Leeds, explored the combined impact of processes in the solid Earth, oceans and atmosphere over the past 400 million years. Their findings are published in the journal Nature Geoscience.

Natural break-down and dissolution of rocks at Earth's surface is called chemical . It is critically important because the products of weathering (elements like calcium and magnesium) are flushed via rivers to the oceans, where they form minerals that lock up CO2. This feedback mechanism regulates atmospheric CO2 levels, and in turn , over .

"In this respect, weathering of the Earth's surface serves as a geological thermostat", says lead author Dr. Tom Gernon, Associate Professor in Earth Science at the University of Southampton, and a Fellow of the Turing Institute. "But the underlying controls have proven difficult to determine due to the complexity of the Earth system".

Volcanoes acted as a safety valve for Earth’s long-term climate
Present-day continental arc volcano in the Kamchatka Peninsula, Russian Far East. Credit: Tom Gernon, University of Southampton

"Many Earth processes are interlinked, and there are some major time lags between processes and their effects", explains Eelco Rohling, Professor in Ocean and Climate Change at ANU and co-author of the study. "Understanding the relative influence of specific processes within the Earth system response has therefore been an intractable problem".

To unravel the complexity, the team constructed a novel "Earth network", incorporating machine-learning algorithms and plate tectonic reconstructions. This enabled them to identify the dominant interactions within the Earth system, and how they evolved through time.

The team found that continental volcanic arcs were the most important driver of weathering intensity over the past 400 million years. Today, continental arcs comprise chains of volcanoes in, for example, the Andes in South America, and the Cascades in the US. These volcanoes are some of the highest and fastest eroding features on Earth. Because the  are fragmented and chemically reactive, they are rapidly weathered and flushed into the oceans.

Martin Palmer, Professor of Geochemistry at the University of Southampton and co-author of the study, said: "It's a balancing act. On one hand, these volcanoes pumped out large amounts of CO2 that increased atmospheric CO2 levels. On the other hand, these same volcanoes helped remove that carbon via rapid weathering reactions."

Volcanoes acted as a safety valve for Earth’s long-term climate
Global chemical weathering has been dominated by volcanic arcs over the past 400 million years (pictured: a river draining Bakening volcano, Kamchatka Peninsula, Russia). Credit: Tom Gernon, University of Southampton

The study casts doubt on a long-held concept that Earth's climate stability over tens to hundreds of millions of years reflects a balance between weathering of the seafloor and continental interiors. "The idea of such a geological tug of war between the landmasses and the seafloor as a dominant driver of Earth surface weathering is not supported by the data," Dr. Gernon states.

"Unfortunately, the results do not mean that nature will save us from climate change", stresses Dr. Gernon. "Today, atmospheric CO2 levels are higher than at any time in the past 3 million years, and human-driven emissions are about 150 times larger than volcanic CO2 emissions. The continental arcs that appear to have saved the planet in the deep past are simply not present at the scale needed to help counteract present-day CO2 emissions".

But the team's findings still provide critical insights into how society might manage the current climate crisis. Artificially enhanced rock weathering—where rocks are pulverized and spread across land to speed up chemical reaction rates—could play a key role in safely removing CO2 from the atmosphere. The team's findings suggest that such schemes may be deployed optimally by using calc-alkaline volcanic materials (those containing calcium, potassium and sodium), like those found in continental arc environments.

"This is by no means a silver bullet solution to the climate crisis—we urgently need to reduce CO2 emissions in line with IPCC mitigation pathways, full stop. Our assessment of weathering feedbacks over long timescales may help in designing and evaluating large-scale enhanced weathering schemes, which is just one of the steps needed to counteract global climate change", Dr. Gernon concludes.


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More information: Global chemical weathering dominated by continental arcs since the mid-Palaeozoic, Nature Geoscience (2021). DOI: 10.1038/s41561-021-00806-0 , www.nature.com/articles/s41561-021-00806-0
Journal information: Nature Geoscience