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Study uncovers source of Mars' redness — a key indicator the planet (maybe) once had life

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Saturday, March 1, 2025

The first thing most people think of when they consider Mars is its deep red color. The Romans associated the planet with their god of war because it reminded them of blood while ​​the Egyptians called it "Her Desher," meaning "the red one." The planet didn’t get such a distinctive, rosy color by accident of course — but for the first time researchers have identified a single mineral they believe is responsible for Martian redness — and that mineral’s presence also indicates the potential presence of life. A new study in the journal Nature Communications reveals that Mars is red for very much the same reason it may have once been home to life — namely, that it was a wet planet. This is in line with research from last year that detailed how Mars was covered in bodies of water in its distant past. “Mars once had liquid water on its surface in rivers, lakes and possibly oceans,” Dr. Michael Manga, the chair of the University of California — Berkeley’s Department of Earth and Planetary Science, told Salon at the time. “We knew that the liquid water being buried deep in the subsurface was one possible solution to the question of where Mars' ancient liquid surface water went.” "The presence of ferrihydrite tells us something specific about Mars' past environment." Mars lost most of that liquid water, which is considered an essential ingredient for life anywhere in the universe. But importantly, this study notes that Mars' redness happened before the water left. So how did a wet planet become so red?  It all comes down to ferrihydrite, a poorly crystalline mineral, or a substance where the atoms or molecules are not arranged in well-defined and repeating patterns. It contains iron oxide, a chemical compound humans traditionally associate with a different reddish-orange substance: rust. Indeed, this mineral exists on our planet, often in volcanic settings such as lava caves. Using state-of-the-art equipment, as well as firsthand analyses of Martian dust from the red planet’s surface, the researchers found that “ferrihydrite remains stable under present-day Martian conditions, preserving its poorly crystalline structure.” This in turn suggests that the ferrihydrite “formed during a cold, wet period on early Mars under oxidative conditions, followed by a transition to the current hyper-arid environment.” In contrast to the conventional wisdom that Mars was continuously dry while its surface oxidized (or was exposed to oxygen), the new study suggests “ancient Mars experienced aqueous alteration before transitioning to its current desert state.” Want more health and science stories in your inbox? Subscribe to Salon's weekly newsletter Lab Notes. Dr. Adomas Valantinas, the paper’s lead author and a postdoctoral fellow at Brown University's Department of Earth, Environmental and Planetary Sciences, explained to Salon that the research team performed extensive spectral analyses on both orbital and rover data in their laboratory. “We can now be quite confident that ferrihydrite is the dominant iron-bearing mineral causing Mars' distinctive ochre color,” Valentinas said. “Our research demonstrated that ferrihydrite provides significantly better fits than other iron oxides like hematite, goethite or akaganeite. We also employed Mars simulation experiments and theoretical calculations to show that ferrihydrite is thermodynamically stable on the Martian surface.” Mars Dust Storm (Getty Images/MARK GARLICK/SCIENCE PHOTO LIBRARY)Similarly, Valentinas explained that the prevalence of this ferrihydrite proves that Mars was once covered in enough water that it was quite wet. That strengthens arguments suggesting Mars was once home to life. “The finding is relevant to inferring the conditions of early Mars as the composition of minerals on the Mars surface tell us about the past climate,” Dr. Geronimo Villanueva, the associate director for Strategic Science of the Solar System Exploration Division at NASA’s Goddard Space Flight Center, and co-author of this study, told Salon. “Importantly, the new findings suggest a wetter and potentially more habitable past for Mars because ferrihydrite forms in the presence of cool water, and at lower temperatures than other previously considered minerals, like hematite.”  Villanueva added that scientists already knew Martian dust contains a number of minerals, including iron oxides; this study narrows down the number of potential iron oxides that could cause the distinctive red color to just one, ferrihydrite. “The presence of ferrihydrite tells us something specific about Mars' past environment,” Valentinas said, describing the cold and pH neutral waters that must have existed to oxidize the soil. “This suggests that rather than warm conditions, early Mars experienced a cold and wet environment.”   To learn this, scientists at the University of Arkansas recreated the arid conditions which exist on Mars, in particular the average temperature of −70 °C and very low water vapor content. Over the course of 40-day laboratory experiments involving dehydration, the scientists learned that ferrihydrite loses some absorbed H2O while maintaining its poorly-crystalline structure. In addition to ferrihydrite the researchers used various quantities of iron oxide phases like magnetite, hematite, feroxyhyte and schwertmannite. Dr. Avi Loeb, a Harvard University astronomer not associated with the study, emphasized the significance of discovering ferrihydrite. “This material likely formed during water activity on early Mars,” Loeb said. “Subsequently, Mars became as dry as we see it today, preserving this mineral phase over its surface. The widespread presence of ferrihydrite in the Martian surface materials was not interpreted this way before, and was thought to be the result of dry oxidation late in Mars history.” Loeb, who has long advocated that scientists seriously explore the possible existence of extraterrestrial life, added that he is impressed with the study’s potential implications on that question. “On Earth, the majority of atmospheric oxygen is derived from biological activity, making the nature of surface oxidation important for understanding the potential for past life on Mars,” Loeb said. Despite these impressive findings, Valentinas emphasized that more research needs to be done on this subject. “Science always leaves room for testing and refinement, so we'll be able to test this hypothesis when the NASA-ESA Mars Sample Return mission brings actual dust samples back to Earth in the 2030s,” Valentinas said. He added that scientists “still don't know the original source location of the ferrihydrite before it was distributed globally through dust storms, the exact chemical composition of Mars' atmosphere when the ferrihydrite formed, or the precise timing of Mars' oxidation.” In addition to encouraging professional scholars to do research, Valentinas urged ordinary citizens to take a crack at looking at the Martian surface. “The Mars rover and orbiter data is fully available to the public,” Valentinas said. “Anyone with access to the internet can download and view the images for themselves under NASA's Planetary Data System.”

Mars became red before it lost its oceans, challenging previous assumptions about its geologic history

The first thing most people think of when they consider Mars is its deep red color. The Romans associated the planet with their god of war because it reminded them of blood while ​​the Egyptians called it "Her Desher," meaning "the red one." The planet didn’t get such a distinctive, rosy color by accident of course — but for the first time researchers have identified a single mineral they believe is responsible for Martian redness — and that mineral’s presence also indicates the potential presence of life.

A new study in the journal Nature Communications reveals that Mars is red for very much the same reason it may have once been home to life — namely, that it was a wet planet. This is in line with research from last year that detailed how Mars was covered in bodies of water in its distant past.

“Mars once had liquid water on its surface in rivers, lakes and possibly oceans,” Dr. Michael Manga, the chair of the University of California — Berkeley’s Department of Earth and Planetary Science, told Salon at the time. “We knew that the liquid water being buried deep in the subsurface was one possible solution to the question of where Mars' ancient liquid surface water went.”

"The presence of ferrihydrite tells us something specific about Mars' past environment."

Mars lost most of that liquid water, which is considered an essential ingredient for life anywhere in the universe. But importantly, this study notes that Mars' redness happened before the water left. So how did a wet planet become so red? 

It all comes down to ferrihydrite, a poorly crystalline mineral, or a substance where the atoms or molecules are not arranged in well-defined and repeating patterns. It contains iron oxide, a chemical compound humans traditionally associate with a different reddish-orange substance: rust. Indeed, this mineral exists on our planet, often in volcanic settings such as lava caves. Using state-of-the-art equipment, as well as firsthand analyses of Martian dust from the red planet’s surface, the researchers found that “ferrihydrite remains stable under present-day Martian conditions, preserving its poorly crystalline structure.”

This in turn suggests that the ferrihydrite “formed during a cold, wet period on early Mars under oxidative conditions, followed by a transition to the current hyper-arid environment.” In contrast to the conventional wisdom that Mars was continuously dry while its surface oxidized (or was exposed to oxygen), the new study suggests “ancient Mars experienced aqueous alteration before transitioning to its current desert state.”


Want more health and science stories in your inbox? Subscribe to Salon's weekly newsletter Lab Notes.


Dr. Adomas Valantinas, the paper’s lead author and a postdoctoral fellow at Brown University's Department of Earth, Environmental and Planetary Sciences, explained to Salon that the research team performed extensive spectral analyses on both orbital and rover data in their laboratory.

“We can now be quite confident that ferrihydrite is the dominant iron-bearing mineral causing Mars' distinctive ochre color,” Valentinas said. “Our research demonstrated that ferrihydrite provides significantly better fits than other iron oxides like hematite, goethite or akaganeite. We also employed Mars simulation experiments and theoretical calculations to show that ferrihydrite is thermodynamically stable on the Martian surface.”

Mars Dust StormMars Dust Storm (Getty Images/MARK GARLICK/SCIENCE PHOTO LIBRARY)Similarly, Valentinas explained that the prevalence of this ferrihydrite proves that Mars was once covered in enough water that it was quite wet. That strengthens arguments suggesting Mars was once home to life.

“The finding is relevant to inferring the conditions of early Mars as the composition of minerals on the Mars surface tell us about the past climate,” Dr. Geronimo Villanueva, the associate director for Strategic Science of the Solar System Exploration Division at NASA’s Goddard Space Flight Center, and co-author of this study, told Salon. “Importantly, the new findings suggest a wetter and potentially more habitable past for Mars because ferrihydrite forms in the presence of cool water, and at lower temperatures than other previously considered minerals, like hematite.” 

Villanueva added that scientists already knew Martian dust contains a number of minerals, including iron oxides; this study narrows down the number of potential iron oxides that could cause the distinctive red color to just one, ferrihydrite.

“The presence of ferrihydrite tells us something specific about Mars' past environment,” Valentinas said, describing the cold and pH neutral waters that must have existed to oxidize the soil. “This suggests that rather than warm conditions, early Mars experienced a cold and wet environment.”  

To learn this, scientists at the University of Arkansas recreated the arid conditions which exist on Mars, in particular the average temperature of −70 °C and very low water vapor content. Over the course of 40-day laboratory experiments involving dehydration, the scientists learned that ferrihydrite loses some absorbed H2O while maintaining its poorly-crystalline structure. In addition to ferrihydrite the researchers used various quantities of iron oxide phases like magnetite, hematite, feroxyhyte and schwertmannite.

Dr. Avi Loeb, a Harvard University astronomer not associated with the study, emphasized the significance of discovering ferrihydrite.

“This material likely formed during water activity on early Mars,” Loeb said. “Subsequently, Mars became as dry as we see it today, preserving this mineral phase over its surface. The widespread presence of ferrihydrite in the Martian surface materials was not interpreted this way before, and was thought to be the result of dry oxidation late in Mars history.”

Loeb, who has long advocated that scientists seriously explore the possible existence of extraterrestrial life, added that he is impressed with the study’s potential implications on that question.

“On Earth, the majority of atmospheric oxygen is derived from biological activity, making the nature of surface oxidation important for understanding the potential for past life on Mars,” Loeb said.

Despite these impressive findings, Valentinas emphasized that more research needs to be done on this subject.

“Science always leaves room for testing and refinement, so we'll be able to test this hypothesis when the NASA-ESA Mars Sample Return mission brings actual dust samples back to Earth in the 2030s,” Valentinas said.

He added that scientists “still don't know the original source location of the ferrihydrite before it was distributed globally through dust storms, the exact chemical composition of Mars' atmosphere when the ferrihydrite formed, or the precise timing of Mars' oxidation.”

In addition to encouraging professional scholars to do research, Valentinas urged ordinary citizens to take a crack at looking at the Martian surface.

“The Mars rover and orbiter data is fully available to the public,” Valentinas said. “Anyone with access to the internet can download and view the images for themselves under NASA's Planetary Data System.”

Read the full story here.
Photos courtesy of

New electronic “skin” could enable lightweight night-vision glasses

MIT engineers developed ultrathin electronic films that sense heat and other signals, and could reduce the bulk of conventional goggles and scopes.

MIT engineers have developed a technique to grow and peel ultrathin “skins” of electronic material. The method could pave the way for new classes of electronic devices, such as ultrathin wearable sensors, flexible transistors and computing elements, and highly sensitive and compact imaging devices. As a demonstration, the team fabricated a thin membrane of pyroelectric material — a class of heat-sensing material that produces an electric current in response to changes in temperature. The thinner the pyroelectric material, the better it is at sensing subtle thermal variations.With their new method, the team fabricated the thinnest pyroelectric membrane yet, measuring 10 nanometers thick, and demonstrated that the film is highly sensitive to heat and radiation across the far-infrared spectrum.The newly developed film could enable lighter, more portable, and highly accurate far-infrared (IR) sensing devices, with potential applications for night-vision eyewear and autonomous driving in foggy conditions. Current state-of-the-art far-IR sensors require bulky cooling elements. In contrast, the new pyroelectric thin film requires no cooling and is sensitive to much smaller changes in temperature. The researchers are exploring ways to incorporate the film into lighter, higher-precision night-vision glasses.“This film considerably reduces weight and cost, making it lightweight, portable, and easier to integrate,” Xinyuan Zhang, a graduate student in MIT’s Department of Materials Science and Engineering (DMSE). “For example, it could be directly worn on glasses.”The heat-sensing film could also have applications in environmental and biological sensing, as well as imaging of astrophysical phenomena that emit far-infrared radiation.What’s more, the new lift-off technique is generalizable beyond pyroelectric materials. The researchers plan to apply the method to make other ultrathin, high-performance semiconducting films.Their results are reported today in a paper appearing in the journal Nature. The study’s MIT co-authors are first author Xinyuan Zhang, Sangho Lee, Min-Kyu Song, Haihui Lan, Jun Min Suh, Jung-El Ryu, Yanjie Shao, Xudong Zheng, Ne Myo Han, and Jeehwan Kim, associate professor of mechanical engineering and of materials science and engineering, along with researchers at the University Wisconsin at Madison led by Professor Chang-Beom Eom and authors from multiple other institutions.Chemical peelKim’s group at MIT is finding new ways to make smaller, thinner, and more flexible electronics. They envision that such ultrathin computing “skins” can be incorporated into everything from smart contact lenses and wearable sensing fabrics to stretchy solar cells and bendable displays. To realize such devices, Kim and his colleagues have been experimenting with methods to grow, peel, and stack semiconducting elements, to fabricate ultrathin, multifunctional electronic thin-film membranes.One method that Kim has pioneered is “remote epitaxy” — a technique where semiconducting materials are grown on a single-crystalline substrate, with an ultrathin layer of graphene in between. The substrate’s crystal structure serves as a scaffold along which the new material can grow. The graphene acts as a nonstick layer, similar to Teflon, making it easy for researchers to peel off the new film and transfer it onto flexible and stacked electronic devices. After peeling off the new film, the underlying substrate can be reused to make additional thin films.Kim has applied remote epitaxy to fabricate thin films with various characteristics. In trying different combinations of semiconducting elements, the researchers happened to notice that a certain pyroelectric material, called PMN-PT, did not require an intermediate layer assist in order to separate from its substrate. Just by growing PMN-PT directly on a single-crystalline substrate, the researchers could then remove the grown film, with no rips or tears to its delicate lattice.“It worked surprisingly well,” Zhang says. “We found the peeled film is atomically smooth.”Lattice lift-offIn their new study, the MIT and UW Madison researchers took a closer look at the process and discovered that the key to the material’s easy-peel property was lead. As part of its chemical structure, the team, along with colleagues at the Rensselaer Polytechnic Institute, discovered that the pyroelectric film contains an orderly arrangement of lead atoms that have a large “electron affinity,” meaning that lead attracts electrons and prevents the charge carriers from traveling and connecting to another materials such as an underlying substrate. The lead acts as tiny nonstick units, allowing the material as a whole to peel away, perfectly intact.The team ran with the realization and fabricated multiple ultrathin films of PMN-PT, each about 10 nanometers thin. They peeled off pyroelectric films and transfered them onto a small chip to form an array of 100 ultrathin heat-sensing pixels, each about 60 square microns (about .006 square centimeters). They exposed the films to ever-slighter changes in temperature and found the pixels were highly sensitive to small changes across the far-infrared spectrum.The sensitivity of the pyroelectric array is comparable to that of state-of-the-art night-vision devices. These devices are currently based on photodetector materials, in which a change in temperature induces the material’s electrons to jump in energy and briefly cross an energy “band gap,” before settling back into their ground state. This electron jump serves as an electrical signal of the temperature change. However, this signal can be affected by noise in the environment, and to prevent such effects, photodetectors have to also include cooling devices that bring the instruments down to liquid nitrogen temperatures.Current night-vision goggles and scopes are heavy and bulky. With the group’s new pyroelectric-based approach, NVDs could have the same sensitivity without the cooling weight.The researchers also found that the films were sensitive beyond the range of current night-vision devices and could respond to wavelengths across the entire infrared spectrum. This suggests that the films could be incorporated into small, lightweight, and portable devices for various applications that require different infrared regions. For instance, when integrated into autonomous vehicle platforms, the films could enable cars to “see” pedestrians and vehicles in complete darkness or in foggy and rainy conditions. The film could also be used in gas sensors for real-time and on-site environmental monitoring, helping detect pollutants. In electronics, they could monitor heat changes in semiconductor chips to catch early signs of malfunctioning elements.The team says the new lift-off method can be generalized to materials that may not themselves contain lead. In those cases, the researchers suspect that they can infuse Teflon-like lead atoms into the underlying substrate to induce a similar peel-off effect. For now, the team is actively working toward incorporating the pyroelectric films into a functional night-vision system.“We envision that our ultrathin films could be made into high-performance night-vision goggles, considering its broad-spectrum infrared sensitivity at room-temperature, which allows for a lightweight design without a cooling system,” Zhang says. “To turn this into a night-vision system, a functional device array should be integrated with readout circuitry. Furthermore, testing in varied environmental conditions is essential for practical applications.”This work was supported by the U.S. Air Force Office of Scientific Research.

President of Eugene wood treatment plant gets 90-day prison term for lying to DEQ inspectors

"There has to be some accountability," U.S. District Judge Michael J. McShane said.

A federal judge Tuesday sentenced the president of Eugene’s J.H. Baxter & Co. wood treatment plant to 90 days in prison for lying about the company’s illegal handling of hazardous waste at the site.U.S. District Judge Michael J. McShane called Georgia Baxter-Krause, 62, an “absent president” who took little responsibility for what occurred.“The fact that you lied when confronted suggests you knew the practice was not ‘above board,’” McShane said. “There has to be some accountability.”He also ordered Baxter-Krause and the company to pay $1.5 million in criminal fines. The plant is now a potential cleanup site under the federal Superfund program.J.H. Baxter & Co. Inc. pleaded guilty to illegally treating hazardous waste and Baxter-Krause pleaded guilty to two counts of making false statements in violation of the Resource Conservation and Recovery Act governing hazardous waste management.The company so far has paid $850,000 of its $1 million share of the fine, and Baxter-Krause has paid $250,000 of her $500,000 share, their attorney David Angeli said.Much of the debate at the sentencing focused on whether Baxter-Krause should go to prison for lying to investigators.According to court documents, J.H. Baxter used hazardous chemicals to treat and preserve wood. Water from the process was considered hazardous waste. The company operated a legal wastewater treatment unit, but for years when there was “too much water on site,” the company essentially would “boil” off the wastewater, allowing discharge into the air through open vents, according to court records.Photograph sent to Georgia Baxter-Krause on July 8, 2019, depicting the inside of a J.H. Baxter container after weeks of boiling hazardous waste, according to federal prosecutors.U.S. Attorney's OfficeAngeli argued that the violations at the Eugene plant were “less egregious” than other criminal environmental damage cases and that “everyone” on the premises thought the hazardous waste handling was OK. He sought probation for Baxter-Krause.“Every person said she never directed or managed this activity,” Angeli said. “She was rarely even in Eugene.”But Assistant U.S. Attorney William McLaren said Baxter-Krause blatantly lied when inspectors from the Oregon Department of Environmental Quality requested information about the company’s practice of boiling off the wastewater.Baxter-Krause provided false information when questioned about the extent of the illegal activity and failed to disclose that the company kept detailed logs that tracked it, according to prosecutors.The plant illegally boiled about 600,000 gallons of wastewater on 136 days from January to October 2019, McLaren said.The government didn’t seek the maximum fine for the environmental violations, which would have been $7 million for each day a violation was found, he said. A separate civil class-action suit is pending against the company filed by people living near the West Eugene plant. They allege gross negligence that allowed “carcinogenic and poisonous chemicals’’ to be regularly released into the air and groundwater. Baxter-Krause told an investigator that the company didn’t keep records on the boiling dates and claimed it occurred only occasionally during the rainy season, records said.“Those were not minimal or immaterial slip-ups,” McLaren said. What the company was doing was “known for years on end” and it was occurring every month, he said.“Despite alerts about equipment failure and the need for capital upgrades, the evidence reflects those warnings went unheeded by J.H. Baxter’s leadership for years,” McLaren said. “And by early 2019, this illegal boiling became the company’s sole method for treating their hazardous wastewater.”Baxter-Krause, who took over the company in 2001 after her father’s death, apologized to the community around the plant and to her friends and family. She now lives in Bend but had lived in California throughout her tenure as company president and visited the Eugene facility about three times a year, according to her lawyers.“I should have been honest,” she said. “To the West Eugene community who was impacted by my careless actions, I apologize. Not a day goes by that I don’t feel remorse. I am ashamed of what I have done. I feel I have truly let you down.”She acknowledged that as president, “the buck stops with me. I should have been more proactive in fully understanding the facility’s permits, the day-to-day operations and ensuring full compliance with environmental laws.”J.H. Baxter treated wood products at the plant from 1943 to 2022. Chemicals used to treat wood, such as creosote and pentachlorophenol, also known as “penta” or PCP, have contaminated the soil and groundwater and are an ongoing concern for surrounding neighborhoods, according to the government.The chemicals remain in tanks at the site and the environmental contamination has not been addressed, according to the Environmental Protection Agency.The company has spent more than $2 million since the plant’s closure to secure the facility and work on complying with environmental regulations, but it has been unable to sell the property because of the historical contamination, according to court records.The judge said it will be up to the Federal Bureau of Prisons where to send Baxter-Krause to serve the sentence. The defense said it would request that she be placed in a community corrections setting.Baxter-Krause was ordered to surrender on July 17. She wondered aloud in the courtroom after her sentencing how she would maintain the compliance reports.Her lawyers explained that the Environmental Protection Agency is on site daily working to fully shut the property down.The EPA is still working to determine how to handle and remove chemicals from the site. It collected soil, sediment, and water samples in May 2023 from both the facility and the surrounding areas. These samples will determine the environmental and potential public health impacts of chemicals that have migrated from the site and from air pollution from its operations.-- Maxine Bernstein covers federal court and criminal justice. Reach her at 503-221-8212, mbernstein@oregonian.com, follow her on X @maxoregonian, on Bluesky @maxbernstein.bsky.social or on LinkedIn.

Your Clothes Are Shedding Bits of Plastic. Here’s What People Are Doing About It This Earth Day

Plastic is everywhere — and yet some people may be surprised at how much they actually wear

Bottles and bags, food wrappers and straws. Piping, packaging, toys and trays. Plastic is everywhere — and yet some people may be surprised at how much they actually wear.A typical closet is loaded with plastic, woven into polyester activewear, acrylic sweaters, nylon swimsuits and stretchy socks — and it’s shedding into the environment nonstop.Even natural fabrics shed fibers and have chemicals that can leach into the environment. But polyester is the most widely used fiber on Earth, and along with other synthetic fibers accounts for about two-thirds of production worldwide. Tuesday is Earth Day, when people worldwide contemplate ways to reduce their impact on the planet.“Everyone who wears and launders clothing is part of this problem but everyone who wears and launders clothing can be part of the solutions,” said Rachael Z. Miller, founder of Vermont-based Rozalia Project for a Clean Ocean.Simple changes like washing clothes less and using cold water instead of hot can help reduce the shedding of fibers. More challenging is that textiles need to be produced and used in a more sustainable way, said Elisa Tonda at the UN Environment Programme. For example, designing clothes that shed fewer microfibers and are high-quality to last longer, said Tonda, who leads the resources and markets branch. What to do? Start by changing habits The easiest solution is to wash clothes less often, making for less of the friction that breaks fibers apart, said Anja Brandon, director of plastics policy at Ocean Conservancy.“They get tumbled and tossed around with a bunch of soaps, really designed to shake things up to get out dirt and stains,” Brandon said. Miller uses a stain stick to spot-clean. Both say that when clothes are washed, they shed less when put in cold water in full loads to reduce friction, on a shorter cycle, then hung to dry.Inspired by the way coral filters the ocean, Miller invented the Cora Ball, a laundry ball that can be tossed into the washer to cut down on clothes banging into each other. It also catches microfibers. (A portion of the proceeds goes to the Rozalia Project.) Another option is to put synthetic fabrics in a washing bag that captures fibers.Miller said people don't need to rush to throw out clothing that's more likely to shed. She owns fleece jackets herself. Instead, she suggested such clothing can be worn indoors only or outside with a layer on top, and it's worth thinking twice about acquiring more garments like that.“I try not to guilt or panic people because a lot of this information is very new,” Miller said. “And so we might as well just say, ‘OK, I got it. How can I be strategic about what I’ve got?’” A push to require filters Filters can be added to washers to capture microfibers. Samsung Electronics collaborated with Patagonia and the global conservation organization Ocean Wise to launch one in 2023. It's now sold in more than 20 countries for front-load washers. Bosch recently launched a microfiber filter in Europe for washers.France was first to adopt a law to mandate that new washing machines sold in the country have a microfiber filter, though implementation has been delayed.In the U.S., efforts to mandate filters in states have failed. California Gov. Gavin Newsom vetoed a bill in 2023, saying he was concerned about the cost to consumers and he wants to incentivize, not mandate, technologies to remove microfibers in wastewater. In Oregon, state Sen. Deb Patterson proposed a bill this year requiring microfiber filters on new washers sold in that state after she came across the technology in Canada. Patterson said the bill doesn't have enough support yet but she'll keep trying. The Association of Home Appliance Manufacturers opposes the proposals, saying it's concerned about consumer costs and filter effectiveness.Some big brands are testing their fabrics to help researchers understand fiber fragmentation, including Adidas, Nike, Patagonia and Under Armour.They're among more than 90 brands, retailers and manufacturers to partner with The Microfibre Consortium in the United Kingdom, founded in 2018 to do research and offer solutions to transform textile production — including reducing fiber breakup.Nearly 1,500 fabrics have been tested. None are the same, making it a tough problem to solve, consortium CEO Kelly Sheridan said. Patagonia has been a leader in trying to stop the spread of synthetic fiber waste into air and water, saying it's up to garment brands to prevent it at the source since cleaning up microplastics in the environment is not yet possible. It paid for its own research starting a decade ago on the implication of its clothes. The company worked with suppliers to choose fabrics and dyes and to finish their clothing in ways that reduce shedding. They collaborated on new filtration technologies for washers, textile mills and municipal systems.One of their best-known styles is something called the “better sweater" that shifts from virgin polyester to recycled polyester to cut shedding by about 40%, said Matt Dwyer, vice president of global product footprint. And at textile mills, there's a prewash at the factory that can capture that first big shed, he added.Dwyer is optimistic about progress.“There’s a whole lot of smart people, not just understanding the problem and the scope of the problem, but also looking for solutions all the way through the manufacturing cycle and use phase,” he said. “Compared to 10 years ago, it’s a whole new world.”The Associated Press’ climate and environmental coverage receives financial support from multiple private foundations. AP is solely responsible for all content. Find AP’s standards for working with philanthropies, a list of supporters and funded coverage areas at AP.org.Copyright 2025 The Associated Press. All rights reserved. This material may not be published, broadcast, rewritten or redistributed.Photos You Should See - Feb. 2025

Potentially Harmful Chemicals Found In Kids' Mattresses

By Dennis Thompson HealthDay ReporterTUESDAY, April 22, 2025 (HealthDay News) — Babies and toddlers could be exposed to harmful chemicals while...

By Dennis Thompson HealthDay ReporterTUESDAY, April 22, 2025 (HealthDay News) — Babies and toddlers could be exposed to harmful chemicals while they sleep, due to compounds found in their mattresses, two new studies say.Air samples taken from 25 children’s bedrooms revealed elevated levels of more than two dozen phthalates, flame retardants and other potentially hazardous chemicals, one of the studies says.In a second study, researchers analyzed 16 newly purchased children’s mattresses and confirmed they are likely the major source of these chemical in kids’ bedrooms.When researchers simulated a child’s body temperature and weight on the mattresses, chemical emissions increased dramatically, according to the study in Environmental Science & Technology."Sleep is vital for brain development, particularly for infants and toddlers,” said senior researcher Miriam Diamond, a professor of environmental science at the University of Toronto.“However, our research suggests that many mattresses contain chemicals that can harm kids’ brains,” she added in a news release. “This is a wake-up call for manufacturers and policymakers to ensure our children’s beds are safe and support healthy brain development.”The phthalates and flame retardants measured in this study are hormone disruptors, researchers said. hormone disruptors — chemicals that interfere with the body's own hormone system — have been linked to brain concerns including learning disorders, reduced IQ, behavioral problems and impaired memory.Children are uniquely vulnerable to exposure from these chemicals, because their brains are still developing and they have breathing rates 10 times higher than adults, researchers said.Kids also have more permeable skin and three times the skin surface area relative to their body weight compared to adults, researchers added.The children’s bedrooms were located in Toronto and Ottawa in Canada, and all of the mattresses were purchased in Canada, researchers noted.However, most of the mattresses contained materials sourced from the U.S., Mexico and other countries, and these results are likely to apply to mattresses purchased throughout North America, researchers said."Parents should be able to lay their children down for sleep knowing they are safe and snug,” researcher Arlene Blum, executive director of the Green Science Policy Institute, said in a news release.“Flame retardants have a long history of harming our children’s cognitive function and ability to learn,” she said. “It’s concerning that these chemicals are still being found in children’s mattresses even though we know they have no proven fire-safety benefit, and aren’t needed to comply with flammability standards.”Manufacturers should be more vigilant regarding chemicals used in children’s mattresses, and stronger regulations on their use are needed, researchers argued.In the meantime, researchers said parents can reduce children’s exposure to these chemicals by decluttering their sleeping area — removing unnecessary pillows, blankets and toys.Parents should frequently wash and refresh kids’ bedding and bedclothes, since these can provide a protective barrier against mattress chemicals, researchers added.Undyed or neutral color fabrics are likely safer, because they don’t need chemicals called UV filters that are added to strong colors to protect them against fading in sunlight, researchers said.SOURCE: Green Science Policy Institute, news release, April 15, 2025Copyright © 2025 HealthDay. All rights reserved.

Fears that UK military bases may be leaking toxic ‘forever chemicals’ into drinking water

Bases in Norfolk, Devon and Hampshire face MoD investigation over possible leaching of dangerous PFAS into environmentThree UK military bases have been marked for investigation over fears they may be leaking toxic “forever chemicals” into drinking water sources and important environmental sites.The Ministry of Defence (MoD) will investigate RAF Marham in Norfolk, RM Chivenor in Devon and AAC Middle Wallop in Hampshire after concerns they may be leaching toxic PFAS chemicals into their surroundings. The sites were identified using a new PFAS risk screening tool developed by the Environment Agency (EA) designed to locate and prioritise pollution threats. Continue reading...

Three UK military bases have been marked for investigation over fears they may be leaking toxic “forever chemicals” into drinking water sources and important environmental sites.The Ministry of Defence (MoD) will investigate RAF Marham in Norfolk, RM Chivenor in Devon and AAC Middle Wallop in Hampshire after concerns they may be leaching toxic PFAS chemicals into their surroundings. The sites were identified using a new PFAS risk screening tool developed by the Environment Agency (EA) designed to locate and prioritise pollution threats.RAF Marham and AAC Middle Wallop lie within drinking water safeguard zones. RM Chivenor borders protected shellfish waters, a special area of conservation, and the River Taw – an important salmon river.PFAS, or per- and polyfluoroalkyl substances, are a group of synthetic chemicals widely used in firefighting foams and industrial processes as well as in aconsumer products including waterproof fabrics, non-stick cookware, cosmetics and food packaging. They are known as forever chemicals because they do not break down easily in the environment, and have been found polluting soil and water across the world. Some PFAS build up in the human body over time and have been linked to a range of serious health problems including cancers, immune system disruption and reproductive disorders.Military bases with airfields have used firefighting foams laden with PFAS for decades. Certain chemicals in foams including PFOS, PFOA and PFHxS have been linked to diseases and banned, but they remain in the environment.Prof Hans Peter Arp, from the Norwegian University of Science and Technology, said contamination at UK military sites would not be surprising. “Most, if not all, military bases in Europe and around the world have used vast quantities of firefighting foams that contain PFAS,” he said. “They now have substantial PFAS concentrations in the soil and groundwater beneath them, as well as soaked into the concrete of their buildings.”He warned that PFAS pollution will continue for “decades to centuries” unless immediate local clean-up actions are taken. “These PFAS that are leaching now likely took several decades to get there. There are more PFAS to come.”RAF Puma helicopters above AAC Middle Wallop, Hampshire. Photograph: Neil Watkin/AlamyThis month the Environmental Audit Committee launched a formal inquiry into PFAS contamination and regulation across the UK. Campaigners and scientists warn that until the full scale of PFAS pollution is understood and addressed, the threat to human health and the environment will continue to grow.Alex Ford, professor of biology at the University of Portsmouth, said: “The EA has now identified thousands of high-risk sites around the UK with elevated concentrations of PFAS compounds. These forever chemicals are being detected in our soils, rivers, groundwater, our wildlife – and us.“It is very worrying to hear PFAS is being detected … close to drinking water sources. The quicker we get this large family of chemicals banned the better, as their legacy will outlive everybody alive today.”He added that the cost of cleaning up these pollutants could run into the billions – costs that, he argued, should be footed by the chemical industry.Not all water treatment works can remove PFAS, and upgrades would be costly. A spokesperson for Water UK, which represents the water industry, said: “PFAS pollution is a huge global challenge. We want to see PFAS banned and the development of a national plan to remove it from the environment, which should be paid for by manufacturers.”Prof Crispin Halsall, an environmental chemist at Lancaster University, called for greater transparency and collaboration. “The MoD shouldn’t try to hide things. They should come clean and set up monitoring,” he said.The UK’s monitoring of PFAS is trailing behind the US, where contamination on military sites has been the focus of billions of dollars in federal spending on testing and clean-up operations.In July, the US Environmental Protection Agency and US Army launched a joint project to sample private drinking-water wells near army installations. UK authorities only recently began to investigate the scale of the problem.Brad Creacey, a former US air force firefighter, spent decades training with firefighting foam on military bases across the US and Europe. During fire exercises, Creacey and his colleagues would ignite contaminated jet fuel and extinguish it with AFFF (aqueous film-forming foams) – often wearing old suits that were soaked and never cleaned. On one occasion he was doused in the foams for fun.Twenty years after he had stopped working with the foams, a blood test revealed that Creacey still had high PFOS levels in his blood. He has been diagnosed with thyroid cancer and now suffers from Hashimoto’s disease, high cholesterol and persistent fatigue.“We’ve taken on too much of a lackadaisical attitude about this contamination,” he said. “Unless this is taken seriously, we’re doomed.”Creacey is pursuing compensation through the US Department of Veterans Affairs and a separate lawsuit against 3M and DuPont.Pete Thompson is a former Royal Air Force firefighter who served at several UK airbases including RAF Coningsby in Lincolnshire. During his service he regularly used firefighting foams in training exercises and equipment tests, and said they usually sprayed them directly on to grass fields with no containment.“We used the foam in the back of what was called a TACR 1 – basically a Land Rover with a 450-litre tank of premixed foam on the back. Every six months we had to do a production test to prove that the system worked. That production test we just produced on to the grass … there was no way of stopping it going anywhere other than just draining in through the ground.”Calm waters at the mouth of the estuary where the River Taw meets the River Torridge in Chivenor, North Devon. Photograph: Terry Mathews/AlamyThe MoD is working with the EA to assess its sites, and work has begun to investigate whether to restrict PFAS in firefighting foams. Military sites are not the only sources of PFAS pollution – commercial airports, firefighting training grounds, manufacturers, landfills, paper mills and metal plating plants can also create contamination problems.An EA spokesperson said: “The global science on PFAS is evolving rapidly, and we are undertaking a multi-year programme to better understand sources of PFAS pollution in England. We have developed a risk screening approach to identify potential sources of PFAS pollution and prioritise the sites for further investigation. We have used this tool to assist the MoD in developing its programme of voluntary investigations and risk assessments.”A government spokesperson said: “There is no evidence that drinking water from our taps exceeds the safe levels of PFAS, as set out by the Drinking Water Inspectorate.“Our rapid review of the Environ­mental Improvement Plan will look at the risks posed by PFAS and how best to tackle them to deliver our legally binding targets to save nature.”The guidelines for 48 types of PFAS in drinking water is 0.1 micrograms per litre (100 nanograms per litre).Earlier this year, Watershed Investigations uncovered MoD documents raising concerns that some RAF bases might be hotspots of forever chemical pollution. In 2022, the Guardian reported that Duxford airfield – a former RAF base now owned by the Imperial War Museum – was probably the source of PFOS-contaminated drinking water in South Cambridgeshire. The site is now under investigation by the EA.Patrick Byrne, professor of water science at Liverpool John Moores University, said current monitoring efforts only scratch the surface. “We’re at the tip of the iceberg. We’re only monitoring a handful of PFAS compounds. There are many others we don’t yet fully understand or detect.“There are tests that measure the total PFAS load in water, and we’re finding huge discrepancies between those results and the levels of individual compounds. That tells us there’s a lot more PFAS in the environment than we know.”Even where testing is under way, labs are overwhelmed. “The Environment Agency’s lab is inundated. Private labs can’t keep up either,” he said. “Analytical technology is improving fast – but we’re racing to keep pace.”

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