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These Popular Mushroom Kits Might Be Causing Environmental Harm

These Popular Mushroom Kits Might Be Causing Environmental Harm

Newsweek2 days ago
Based on facts, either observed and verified firsthand by the reporter, or reported and verified from knowledgeable sources.
Newsweek AI is in beta. Translations may contain inaccuracies—please refer to the original content.
Bright yellow golden oyster mushrooms, prized for their nutty flavor and easy cultivation, have surged in popularity thanks to at-home growing kits.
But new research warns that these kits may be unleashing an invasive species into North American forests.
A study conducted by researchers in Wisconsin found that trees colonized by golden oyster mushrooms hosted about half as many native fungal species as those without them.
DNA analysis from elm tree samples showed that the presence of this invasive fungus, Pleurotus citrinopileatus, reduced both the diversity and composition of native fungi.
Stock image of mushrooms.
Stock image of mushrooms.
Photo by chengyuzheng / Getty Images
Aishwarya Veerabahu, a co-author of the study and Ph.D. candidate at the University of Wisconsin-Madison, wrote in The Conversation that the invasive species had displaced fungi such as the mossy maze polypore and the elm oyster.
According to Veerabahu, when native species are pushed out, researchers lose the opportunity to study their potential benefits.
"I think [mushroom growers] very likely could introduce other types of invasive mushrooms," Veerabahu told Newsweek in an email.
"I have my eye on the other non-native species of oyster mushrooms, but in truth it can be any."
'A simple but vital joy'
Fungi serve as natural recyclers, breaking down dead wood and plant material and converting it into nutrients that enrich the soil.
They also support climate regulation by storing carbon and helping other plants absorb water and nutrients.
Disruption to these fungal communities could weaken forest ecosystems already strained by habitat loss and climate change.
Veerabahu added that "the invasion of golden oysters risks erasing a simple, but vital, joy of seeing different, colorful, incredible fungi in the forest".
"Every winter after the snow melts, fungi growing on dead wood are often the first ones to pop up, and I so love to see them again," she told Newsweek. "Golden oysters might make that experience non-existent.
"Fungal biodiversity deserves to exist, period. Moving non-native fungi around the world puts fungal biodiversity at risk, along with everything they have to offer us: vital ecosystem processes, therapeutic medicines, and a deeper understanding of the natural world."
What To Know
The golden oyster mushroom, native to eastern Asia, was introduced to North America in the early 2000s and gained popularity through home-growing kits and cultivation on outdoor logs.
While most cultivated mushrooms remain harmless, golden oysters have spread rapidly since escaping cultivation and are now reported in 25 U.S. states and parts of Canada.
"As far as we know, this is the first cultivated species that has escaped," Veerabahu told Newsweek.
"So even if a few people had an inkling, most people didn't know this could happen, and it's certainly not anyone's fault."
What People Are Saying
Veerabahu urged caution in The Conversation: "I recommend that people consider refraining from using golden oyster mushroom grow kits to prevent any new introductions.
"For people who make a living selling these mushrooms, consider adding a note that this species is invasive and should be cultivated indoors and not composted."
What's Next
Veerabahu told Newsweek she plans to continue studying golden oyster mushrooms.
Specifically, Veerabahu plans to examine whether the mushrooms have evolved to be genetically distinct from native populations.
She also plans to examine the perspectives and priorities of stakeholders in golden oyster mushrooms and how they can be managed going forward.
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Mom Gets All Kids Tested For Daughter's Rare Illness, Worst Fear Comes True
Mom Gets All Kids Tested For Daughter's Rare Illness, Worst Fear Comes True

Newsweek

timea day ago

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Mom Gets All Kids Tested For Daughter's Rare Illness, Worst Fear Comes True

Based on facts, either observed and verified firsthand by the reporter, or reported and verified from knowledgeable sources. Newsweek AI is in beta. Translations may contain inaccuracies—please refer to the original content. When a Long Island toddler was first diagnosed with a rare illness, her family could never have predicted what it would lead to for her older sister. Lisa Superina could tell her daughter Nora was not well from as early as 5 months old. All of her experience as a mother of five told her something wasn't quite right. "She was eating well but often seemed uncomfortable and she wasn't gaining weight," Superina told Newsweek. "She had frequent infections – respiratory and skin. Bad eczema. Her stools were excessive, loose and pale. She seemed very weak with bags under her eyes." Yet despite this, it took time for Superina to get answers. "Nora had genetic testing that all came back negative, so at that point I was told to wait and see what happens," she said. "That was not an option for me... I needed answers. She was my 4th child, so I knew that she wasn't developing typically and something was very wrong." Lisa Superina, her husband and their 5 kids. Lisa Superina, her husband and their 5 kids. Lisa Superina After pushing for more testing, Nora underwent genome sequencing. That was when it was discovered she had Shwachman–Diamond Syndrome (SDS), a rare, inherited bone marrow failure characterized by a low number of white blood cells, poor growth due to difficulty absorbing food, and, in some instances, skeletal abnormalities. Children with SDS can develop blood disorders such as myelodysplastic syndrome (MDS) or leukemia. According to the Boston Children's Hospital, nearly 5 percent of children with SDS develop leukemia, with that risk increasing to 25 percent by adulthood. "This risk goes up with age, so every year gets a little scarier," Superina said. Nora was diagnosed in June 2021, when she was just 15 months old. The rare nature of her illness meant it was not on any doctors' radars when she first began to exhibit symptoms. There would be one more bombshell to come, though. "We were told to test our other children because sometimes SDS is exclusive to the blood and bone marrow and does not have many obvious symptoms," Superina said. A few months later, their worst fears were realized when it was confirmed that Nora's older sister, Kayla, who was just 3 at the time, also had SDS. Though it was a shock to hear, Superina felt some sense of relief that they finally knew about Nora's condition and had uncovered Kayla's before anything bad happened. "I'm so grateful for their diagnosis because it gives us the tools we needed to help them and be proactive," she said. "We know what we are up against." What they are up against is an illness with no known cure, only what Superina describes as "aggressive management." "Nora and Kayla have annual bone marrow biopsies to check for changes or mutations in the marrow that would suggest problems," Superina said. "They get bloodwork every 3 months with hematology at the bone marrow/oncology clinic and see many specialists including hematology, gastroenterology, endocrinology, rheumatology, dermatology, ophthalmology, the list goes on..." It's an experience that has brought the sisters even closer together. "Kayla and Nora have an amazing bond. They support each other for all their appointments... holding hands. Cheering each other on," Superina said. "I definitely think it's made them closer. They don't ever have to go through anything alone- and they always have someone who truly understands." In the meantime, Superina has turned to social media, sharing her daughters' story on Instagram under the handle rarelifemom in the hopes of spreading awareness about SDS and raising essential funds for researching treatments. "I am in touch with top researchers and attended the recent SDS Congress in Cincinnati to learn about the research right now and have been spreading the word for funding a very exciting and promising gene editing project out of Boston Children's with the SDS Registry," she said. "The problem is rare diseases like SDS don't get the funding that more common ones do. So even if we know how to cure it, and have a treatment plan, the money just isn't there. It's often up to the parents and the rare disease community to fund their disease. So that's what I'm trying to do. Raise awareness on social media and who knows, maybe someone with a big heart and a big wallet will see it and want to help my sweet girls."

‘Resident Alien' canceled at USA Network in shocking move ahead of Season 4 finale
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New York Post

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‘Resident Alien' canceled at USA Network in shocking move ahead of Season 4 finale

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'Disabling' Chronic Illness in Children Not Taken Seriously: Experts
'Disabling' Chronic Illness in Children Not Taken Seriously: Experts

Newsweek

time2 days ago

  • Newsweek

'Disabling' Chronic Illness in Children Not Taken Seriously: Experts

Based on facts, either observed and verified firsthand by the reporter, or reported and verified from knowledgeable sources. Newsweek AI is in beta. Translations may contain inaccuracies—please refer to the original content. A new study by Rutgers University has highlighted that a significant number of young children are experiencing ongoing symptoms after COVID-19 infection, signifying that greater research needs to be poured into evaluating the risk and treatment of long COVID in children. The study, released on July 23, coincides with Pediatric Long COVID Awareness Week, running from July 21 to 25, run by the advocacy group Long Covid Families. Over the course of the week, the group has been bringing together families, clinicians, researchers, and advocates to raise more awareness on the wide-reaching impact of long COVID in children. "This is a public health crisis for children. And it demands action," Long Covid Families said in its promotion of the condition's awareness week. 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It can result in a wide range of symptoms, affecting multiple systems in the body. Co-author of the study, Lawrence Kleinman, who is also chair of the Department of Pediatrics at Rutgers University, told Newsweek that he was not "surprised by these findings and would not be surprised to learn in the future that they understate the prevalence of long COVID." Previous studies estimated the prevalence of long COVID in children to be between 10 and 20 percent—suggesting it has become one of the most common chronic illnesses in children. Asthma, often described as the most common chronic illness in children, affects 16 percent. "Our methods were designed to be conservative, that is to maximize the likelihood that we distinguished long COVID from other causes," Kleinman said. "That means that our estimates are likely to be lower than the actual rate of long COVID." "At the beginning of the pandemic, no one knew that long COVID existed," he added. The first reports from China included" inaccurate reports" that children were spared COVID, he said, adding that the reports "grew into a myth which in turn created a mindset that COVID in kids didn't matter." As a result, there "was a misconception that children could not get COVID - but we know that's not true," Melissa Stockwell, another author of the study and chief of the Division of Child and Adolescent Health at Columbia University, told Newsweek. "We are still very behind in raising awareness about long COVID in children," she added. Another reason why long COVID was not taken seriously in children is that "the symptoms associated with long COVID in children were not properly defined," Dr. Akiko Iwasaki, director of the Center for Infection and Immunity at the Yale School of Medicine, told Newsweek. She added that the study underscored "the need for the society to take long COVID in children seriously." However, Dr. Gerald Teague, a professor of pediatrics at the University of Virginia School of Medicine, told Newsweek that the study's investigators "did not confirm COVID infection with diagnostic tests nor did they measure antibodies to COVID in the participants," which would have provided a more accurate screening of the condition. He also noted that children not flagged as having COVID in the study may have had "asymptomatic infection." Although, despite some concerns, he said, with the study, that it was a "proof of concept that long COVID may be a bigger problem than we thought." The Impact Of Long COVID On Children "There is great concern for the younger generation, both about the long-term impacts of the pandemic itself, but also for those with Long Covid," Stockwell said. Long COVID in children can manifest in a number of different symptoms, ranging from "annoying to disabling," Kleinman said. The chronic illness can cause "pain, distress, or disability" in children, directly impacting the child's interaction with their family and friends, and may "hurt school performance, athletic performance, or even the capacity of children to conduct normally routine activities," he added. These factors are of great concern, Al-Aly said, as "we worry about kids' educational attainment, forming friendships, sports, and others, and all of these facets of normal development could be impaired in long COVID." "This may negatively affect kids in their most formative years—leaving them scarred for a lifetime," he added. Long COVID can leave some children bedbound for years, Iwasaki said. "If you have ever spoken to a parent of a child with long COVID, you quickly learn how devastating it can be to the lives of the children and their family," she added. What Experts Think Should Be Done One key part of tackling the issue is down to "improving vaccine uptake," Al-Aly said. However, the Trump administration has recently removed COVID vaccines from the Centers for Disease Control and Prevention (CDC) recommendation for healthy children and pregnant women, as part of Health Secretary Robert F. Kennedy Jr's "Make America Healthy Again" (MAHA) campaign. Kennedy Jr, a well-known vaccine sceptic, said, when announcing the update on X: "It's common sense and it's good science." Another important step is increasing understanding, Stockwell said. "We really need pediatricians to understand what long COVID looks like in children and understand that symptoms are actually different in different-aged children as well," she added. Treatments are the next vital step, Kleinman said. "We need to develop and identify effective treatments for long COVID in a rapidly iterative and long-term approach to quickly identify promising treatments and to evaluate their effectiveness and safety in practice." That treatment, though, needs to "get at the root causes of the disease," Iwasaki said. She added that long COVID is a disease "driven by the virus and the host responses to the virus involving the immune, neurological, cardiovascular, gastrointestinal and pulmonary systems." From a policy perspective, "flexible attendance at school, proper training of teachers and pediatricians, insurance coverage and more funding for research" would all help tackle the issue, Iwasaki added. More broadly, supporting children with long COVID and preventing further cases will require "investment in health and health care services, physical and occupational rehabilitation, and mental health services," Kleinman added, saying this "will be critical for the population health of our children for the foreseeable future."

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