Wednesday, April 23, 2025

 

Hotter temps trigger wetlands to emit more methane as microbes struggle to keep up



Scientists dial up heat and carbon dioxide in futuristic experiment



Smithsonian

Jaehyun Lee 

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Jaehyun Lee collects a porewater sample in the SMARTX experiment, at the Smithsonian Environmental Research Center in Maryland.

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Credit: Smithsonian Environmental Research Center




Rising temperatures could tip the scale in an underground battle that has raged for millennia. In the soils of Earth’s wetlands, microbes are fighting to both produce and consume the powerful greenhouse gas methane. But if the Earth gets too hot, a key way wetlands clamp down on methane could be at risk, according to a Smithsonian study published April 23.

Methane is responsible for roughly 19% of global warming, according to the National Oceanographic and Atmospheric Administration. And while wetlands are champions at removing carbon dioxide (CO2)—the more abundant greenhouse gas—they are also the world’s largest natural source of methane. As nations set targets to bring down methane emitted from human activity, it is crucial to understand how much methane wetlands emit naturally—and how much more they could emit in the future.

“If there is a large amount of methane emissions from wetlands, and if we don’t know anything about that, then our carbon reduction target for mitigating climate change is going to be off track in the future,” said lead author Jaehyun Lee. Lee, who now works at the Korea Institute of Science and Technology, did the study while a postdoctoral fellow at the Smithsonian Environmental Research Center.

Microbial Tug-of-War

In wetland soils, two types of microbes are locked in competition. Some microbes produce methane, a greenhouse gas up to 45 times stronger than CO2. But other microbes consume that methane, using oxygen to turn it into less-harmful CO2. That simple transformation is one of nature’s most powerful ways to keep greenhouse gas emissions in check.

The new study, published in the journal Science Advances, focused on a special class of microbes known as anaerobic. Anaerobic microbes live in places without free oxygen—zones that are quite common in flooded wetlands. For a long time, they have been the underdogs in the methane wars. With no free oxygen to draw from, these microbes were believed to be unable to consume methane. When scientists finally discovered they could (by pulling oxygen from nearby sulfate molecules), they still thought it was a minor background effect compared to the microbes in oxygen-rich parts of the wetland.

“They thought that the anaerobic methane [consumption] process is going to be too slow to remove a significant amount of methane,” Lee said.

But as Lee pointed out, most methane production happens in these oxygen-starved environments. This essentially means anaerobic microbes are on the front lines. And they are pulling their weight. In the Smithsonian wetland Lee worked in, anaerobic microbes can remove up to 12% of the methane—far less than their oxygen-loving counterparts, but more than scientists previously suspected. And in saltier, sulfate-rich places, anaerobic microbes can remove up to 70% of the methane produced in oxygen-deprived soils.

However, things changed when scientists dialed up the heat.

A Fast-Forward Climate Experiment

In the new study, the team simulated a hotter future using an experiment on a wetland at the Smithsonian Environmental Research Center (SERC) in Maryland. The experiment goes by the name “SMARTX” (short for “Salt Marsh Accretion Response to Temperature eXperiment”). Scientists raised the temperature by 5.1 degrees Celsius in certain parts of the wetland by energizing rows of infrared lamps and underground cables. In some plots, the team also raised CO2 to create a more realistic future.

“You’re never going to get a warmer world without also having higher CO2 in the atmosphere….What SMARTX is doing is trying to mimic that warmer world, with the aboveground and belowground heating,” said Genevieve Noyce, a coauthor and senior scientist at SERC. “But because that’s not going to happen independent of CO2, we also cross it with CO2, so we have a real future that has both.”

Methane emissions spiked under hotter temperatures alone. This was not because the helpful microbes became weaker. Warmer soils triggered them to remove even more methane than before. However, their competitors—the microbes that produce methane—became more active as well. And in a warmer world, the methane-removing microbes were unable to keep up.

How much methane emissions went up depended on the plants. In areas dominated by thick sedges, methane emissions rose nearly four times higher. But where smaller grasses prevailed, methane emissions increased only 1.5 times.

Ironically, higher CO2 lessened the impact—but not enough to cancel it out. Methane emissions in the sedge plots rose to just double normal levels, rather than nearly quadrupling, when scientists tested higher temperatures and higher CO2 together. The researchers suspect this is because CO2 triggers plants to grow bigger roots. Roots inject more oxygen into the soil, creating even more oxygen-rich sulfate compounds for the microbes to use.

“Warming is going to have a really big effect on increasing methane emissions,” Noyce said. “But when you add elevated CO2, it kind of brings it back down a little bit.”

This pattern holds for microbes across the entire wetland. In 2021, the team discovered that microbes in oxygen-rich soils behave the same way as the oxygen-starved microbes in this study. When the environment heats up, microbes that remove methane fall further behind their methane-producing cousins.

Conserving wetlands is still a vital part of protecting the world from climate change, the authors said. They are lifesaving buffers from hurricanes and extreme weather. And despite the methane issue, wetlands excel at locking away planet-warming carbon in other forms. An acre of coastal wetland can store more carbon than an acre of tropical rainforest.

“There is great value in protecting and restoring coastal wetlands to benefit climate, especially when we consider the many ecosystem services they provide to people,” said Pat Megonigal, the senior author and associate director of research at SERC.

But to plan for the future, policymakers need to know how much methane wetlands will emit in the decades to come. At the end of the day, Lee said, climate change is not only about hotter temperatures. It is also about the invisible activities that could tip the balance of greenhouse gases.

“We also have to consider, how is climate change going to affect these delicate microbial processes, such as methane oxidation and methane production?” he said.

Yonsei University in Korea was also involved in the research. A copy of the study will be available on the journal’s website after publication. For photos or to speak with one of the authors, contact Kristen Goodhue at GoodhueK@si.edu.   

 

Water quality could be degraded by development and conversion of forests upstream, with sediment levels and nitrogen concentrations also worsened




PLOS
Water quality could be degraded by development and conversion of forests upstream, with sediment levels and nitrogen concentrations also worsened, per modelling analysis of the Middle Chattahoochee watershed of Georgia, Alabama, and Florida 

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Projected land use changes will cause water quality degradation at drinking water intakes across a regional watershed

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Credit: USGS




Water quality could be degraded by development and conversion of forests upstream, with sediment levels and nitrogen concentrations also worsened, per modelling analysis of the Middle Chattahoochee watershed of Georgia, Alabama, and Florida.

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Article URL: https://plos.io/3Gi6Kaq

Article Title: Projected land use changes will cause water quality degradation at drinking water intakes across a regional watershed

Author Countries: United States

Funding: This work was supported by the U.S. Department of Agriculture (USDA) Forest Service Southern Research Station by agreement number 20-CS-11330180-053 to Dr. Katherine Martin at North Carolina State University. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

 

The antibiotic that takes the bite out of Lyme



Study shows specific antibiotic cures Lyme disease at a fraction of the dosage



Northwestern University






  • Current ‘gold standard’ treatment does not work for up to 20% of population and kills beneficial bacteria
  • Scientists screened nearly 500 FDA-approved compounds to assess effectiveness against Lyme
  • Piperacillin effectively treats Lyme disease at 100-times lower dose than doxycycline

CHICAGO --- Lyme disease, a disease transmitted when deer ticks feed on infected animals like deer and rodents, and then bite humans, impacts nearly half a million individuals in the U.S. annually. Even in acute cases, Lyme can be devastating; but early treatment with antibiotics can prevent chronic symptoms like heart and neurological problems and arthritis from developing. 

Scientists from Northwestern University have identified that piperacillin, an antibiotic in the same class as penicillin, effectively cured mice of Lyme disease at 100-times less than the effective dose of doxycycline, the current gold standard treatment. At such a low dose, piperacillin also had the added benefit of “having virtually no impact on resident gut microbes,” according to the study, which will be published April 23 in the journal Science Translational Medicine.

Doxycycline and other generic antibiotics, on the other hand, wreak havoc on the microbiome, killing beneficial bacteria in the gut and causing troubling side effects even as it kills the borrelia bacteria that causes Lyme. In addition to its negative impact on the gut, doxycycline also fails to help between 10 and 20% of individuals who take it, and it is not approved for use in young children — who are at the highest risk of tick bites, and therefore, of developing Lyme.

More effective, or at least more specified, treatment options are needed as climate change extends tick seasons and Lyme becomes more prevalent.

“Powerful, broad-spectrum antibiotics that kill extracellular bacteria are seen as the most effective medication because physicians want to just kill the bacterium and don't care how,” said Brandon L. Jutras, who led the research. “This is certainly a reasonable approach, but I think the future for Lyme disease patients is bright in that we are approaching an era of customized medicine, and we can potentially create a particular drug, or a combination to treat Lyme disease when other fail. The more we understand about the various strains and species of Lyme disease-causing Borrelia, the closer we get to a custom approach.”

Jutras is an associate professor in the microbiology-immunology department of Northwestern University Feinberg School of Medicine, and a member of Northwestern’s Center for Human Immunobiology. Jutras’s lab was recently named a Phase 3 winner in LymeX Diagnostics, the Steven & Alexandra Cohen Foundation’s $10 million competition to accelerate the development of Lyme disease diagnostics, and in 2021 he won the Bay Area Lyme Foundation Emerging Leader Award.

The authors argue that piperacillin, which has already been FDA-approved as a safe treatment for pneumonia, could also be a candidate for preemptive interventions, in which someone potentially exposed to Lyme (with a known deer tick bite) would receive a single-dose shot of the medication.

To reach the conclusion that the penicillin relative would be the most effective and targeted treatment, the team screened nearly 500 medicines in a drug library, using a molecular framework to understand potential interactions between antibiotics and the Borrelia bacteria. Once the group had a short list of potentials, they performed additional physiological, cellular and molecular tests to identify compounds that did not impact other bacteria.

They found that piperacillin exclusively interfered with the unusual cell wall synthesis pattern common to Lyme bacteria, preventing the bacteria from growing or dividing and ultimately leading to its death.

Historically, piperacillin has been administered as part of a two-drug cocktail to treat severe strep infections because strep can break down beta-lactams (piperacillin’s class of antibiotics) unless accompanied by tazobactam, which is an inhibitor of the enzyme that inactivates piperacillin. Jutras wondered if using the same two medications, rather than piperacillin alone, would be a more effective bacteria killer.

“Bacteria are clever,” Jutras said. “Strep and some other bacteria combat antibiotics by secreting beta-lactamases that inactivate piperacillin. We found the approach is totally irrelevant in the context of Lyme disease and another way that makes piperacillin more specific. Adding the beta-lactamase inhibitor doesn’t improve the therapy because Lyme Borrelia don’t produce beta-lactamase, but the cocktail does negatively impact the microbiome by becoming more broadly functional against beneficial residents.”

Lyme prevention remains a challenge — no approved human vaccine exists — and Jutras hopes his research moving forward will help with developing proactive strategies to diagnose and treat it.

The study was supported by the Bay Area Lyme Foundation and United States Department of Agriculture (VA-160113), the Dennis Dean Research Grant (Virginia Tech), the National Institutes of Allergy and Infectious Disease (R01AI173256, R01AI178711), the Steven & Alexandra Cohen Foundation and the Global Lyme Alliance.

 

Engineering a robot that can jump 10 feet high – without legs



Studying a leaping, body-bending parasite thinner than a human hair led Georgia Tech engineers to create a soft robot that can hop forward and backward.



Georgia Institute of Technology

comics nematode 1 

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A comic inspired by the research

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Credit: Saad Bhamla/Georgia Tech





Inspired by the movements of a tiny parasitic worm, Georgia Tech engineers have created a 5-inch soft robot that can jump as high as a basketball hoop.

Their device, a silicone rod with a carbon-fiber spine, can leap 10 feet high even though it doesn’t have legs. The researchers made it after watching high-speed video of nematodes pinching themselves into odd shapes to fling themselves forward and backward.

The researchers described the soft robot April 23 in Science Robotics. They said their findings could help develop robots capable of jumping across various terrain, at different heights, in multiple directions.

“Nematodes are amazing creatures with bodies thinner than a human hair,” said Sunny Kumar, lead coauthor of the paper and a postdoctoral researcher in the School of Chemical and Biomolecular Engineering (ChBE). “They don’t have legs but can jump up to 20 times their body length. That’s like me laying down and somehow leaping onto a three-story building.”

Nematodes, also known as round worms, are among the most abundant creatures on Earth. They live in the environment and within humans, insects, and animals. They can cause illnesses in their host, which sometimes can be beneficial. For instance, farmers and gardeners use nematodes instead of pesticides to kill invasive insects and protect plants.

One way they latch onto their host before entering their bodies is by jumping. Using high-speed cameras, Victor Ortega-Jimenez — a former Georgia Tech research scientist who’s now a faculty member at the University of California, Berkeley — watched the creatures bend their bodies into different shapes based on where they wanted to go.

To hop backward, nematodes point their head up while tightening the midpoint of their body to create a kink. The shape is similar to a person in a squat position. From there, the worm uses stored energy in its contorted shape to propel backward, end over end, just like a gymnast doing a backflip.

To jump forward, the worm points its head straight and creates a kink on the opposite end of its body, pointed high in the air. The stance is similar to someone preparing for a standing broad jump. But instead of hopping straight, the worm catapults upward.

“Changing their center of mass allows these creatures to control which way they jump. We’re not aware of any other organism at this tiny scale that can efficiently leap in both directions at the same height,” Kumar said.

And they do it despite nearly tying their bodies into a knot.

“Kinks are typically dealbreakers,” said Ishant Tiwari, a ChBE postdoctoral fellow and lead coauthor of the study. “Kinked blood vessels can lead to strokes. Kinked straws are worthless. Kinked hoses cut off water. But a kinked nematode stores energy that is used to propel itself in the air.”

After watching their videos, the team created simulations of the jumping nematodes. Then they built soft robots to replicate the leaping worms’ behavior, later reinforcing them with carbon fibers to accelerate the jumps

Kumar and Tiwari work in Associate Professor Saad Bhamla’s lab. They collaborated on the project with Ortega-Jimenez and researchers at the University of California, Riverside.

The group found that the kinks allow nematodes to store more energy with each jump. They rapidly release it — in a tenth of a millisecond — to leap, and they’re tough enough to repeat the process multiple times.

The study suggests that engineers could create simple elastic systems made of carbon fiber or other materials that could withstand and exploit kinks to hop across various terrain.

“A jumping robot was recently launched to the moon, and other leaping robots are being created to help with search and rescue missions, where they have to traverse unpredictable terrain and obstacles,” Kumar said. “Our lab continues to find interesting ways that creatures use their unique bodies to do interesting things, then build robots to mimic them.”

The work was supported by the National Institutes of Health, grant Nos. R35GM142588 and R35GM137934, and the National Science Foundation, grant Nos. PHY-2310691 and CMMI-2218382. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the authors and do not necessarily reflect the view of any funding agency.

Citation: Kumar S, Tiwari I, Ortega-Jimenez V, Dillman A, He D, Hu Y, and Bhamla S, Reversible kink instability drives ultrafast jumping in nematodes and soft robots, Science Robotics 2025. 10.1126/scirobotics.adq3121


A comic inspired by the research 

Credit

Saad Bhamla/Georgia Tech