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Tag: Wildlife

  • Savage Kingdom Season 3 Streaming: Watch & Stream Online via Disney Plus

    Savage Kingdom Season 3 Streaming: Watch & Stream Online via Disney Plus

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    Savage Kingdom Season 3 is the third season of the show consisting of six episodes. It continues the wildlife saga, offering an intimate look into the ongoing battles for survival among Africa’s majestic creatures. Narrated by Charles Dance, the documentary series gives an insight into the intricate dynamics of predator and prey relationships, capturing the relentless struggles for dominance and the pursuit of life in the untamed wilderness.

    Here’s how you can watch and stream Savage Kingdom Season 3 via streaming services such as Disney Plus.

    Is Savage Kingdom Season 3 available to watch via streaming?

    Yes, Savage Kingdom Season 3 is available to watch via streaming on Disney Plus.

    Savage Kingdom Season 3 takes viewers back on a riveting journey into the heart of the African wilderness, showcasing the unyielding battles for survival among its diverse wildlife. The series also captures the intense struggles of predators and prey as they navigate the harsh landscapes. From cunning strategies to fierce confrontations, the show unveils the untamed world’s realities.

    From lions leading prides to cunning hyenas and agile cheetahs, this series showcases these animals in their natural habitat. Narrated by Charles Dance, it offers an intimate look at the lives, struggles, and triumphs of these creatures in their quest for survival.

    Watch Savage Kingdom Season 3 streaming via Disney Plus

    Savage Kingdom Season 3 is available to watch on Disney Plus. It is a family-friendly streaming service with a vast collection of beloved Disney, Pixar, Marvel, Star Wars, and National Geographic content. Subscribers can also enjoy iconic titles such as The Mandalorian, WandaVision, and a vast library of classic animated films, making it a go-to platform for wholesome entertainment across generations.

    You can watch via Disney Plus by following these steps:

    1. Visit DisneyPlus.com
    2. Select ‘Sign Up Now’
    3. Enter your email and password
    4. Select a subscription plan
      • $7.99 per month (Basic)
      • $13.99 per month or $139.99 per year (Premium)
    5. Enter your payment information

    The Disney Plus Basic plan allows users to stream the service’s content with ads, while the Premium plan lets users stream with no ads and download content to supported devices. There are also a variety of bundle packages, scaling from Bundle Duo Basic, which pairs Disney Plus with Hulu for $9.99 per month, to the Disney Bundle Trio Premium for $19.99 per month, which bundles Disney Plus, Hulu, and ESPN Plus.

    The Savage Kingdom official synopsis is as follows:

    “A rare look at warring animal clans battling for survival in a remote region of Africa, which is drying up after years of flood-soaked abundance.”

    NOTE: The streaming services listed above are subject to change. The information provided was correct at the time of writing.

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    Elton Fernandes

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  • Urgent Message from WCS as the Avian Influenza Virus Threatens Wildlife Across the Globe

    Urgent Message from WCS as the Avian Influenza Virus Threatens Wildlife Across the Globe

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    New York, January 15, 2024 – The Wildlife Conservation Society is issuing the following statement about H5N1 Avian Influenza due to ongoing wildlife die-offs across the world:

    Said Dr. Chris Walzer, WCS Executive Director of Health: 

    “With the frightening die-off of animals across the globe due to avian influenza, WCS is calling for governments internationally to treat this growing crisis with the urgency it demands. As we continue to monitor the death of innumerable species and track the movement of highly pathogenic avian influenza (HPAI) into mammal populations, we must strengthen the focus on integrating the surveillance of emerging influenza clades in wild birds and mammals to support critical vaccine libraries.

    “H5N1 now presents an existential threat to the world’s biodiversity. It has infected over 150 wild and domestic avian species around the globe as well as a dozens of mammalian species. The bird flu outbreak is the worst globally and also in U.S. history, with hundreds-of-million birds dead since it first turned up in domestic waterfowl in China in 1996. Bird flu is highly transmissible, spread through droplet and feces-borne infections, and exacerbated by climate-change-altering migration schedules for birds and its repeated re-circulation in domestic poultry. 

    “Globally, HPAI H5N1 has now infected many mammals—including foxes, pumas, skunks, and both black and brown bears in North America. Some 700 endangered Caspian seals died from HPAI near Dagestan in 2023. Additionally, outbreaks in mink farms in Spain and Finland that serve as potential mixing vessels for reassortment have also been documented. HPAI H5N1 has arrived in Latin America with devastating consequences, afflicting multiple countries that include WCS land- and seascapes in Peru, Chile, Uruguay, Ecuador, and Argentina. 

    “More than 95 percent of the Southern elephant seal (Mirounga leonina) pups born along 300 km of the Patagonia coastline died at the end of 2023. It’s the first report of massive elephant seal mortality in the area from any cause in the last half century. The sight of elephant seals found dead or dying along the breeding beaches can only be described as apocalyptic. This 2023 die-off contrasts starkly with the 18,000 pups born and successfully weaned in 2022.  

    “As the virus continues to spread through mammal populations, the World Health Organization (WHO) has called on public health officials to prepare for a potential spillover of H5N1 to people. The “R naught” value—or the number of people infected by a single infected person—for COVID initially ranged from 1.5 to 7. For H5N1 among birds, it is around 100. It is imperative that we take a collaborative One Health approach to identifying emerging strains of bird flu across the globe to support the development of specific and universal vaccines that can quickly treat infection in people to prevent another pandemic.

    “The cost of inaction is already causing major devastation to wildlife. As we work to help affected populations recover, we must remain vigilant against the spread of this deadly pathogen to people before it’s too late. 

     

    Background

    Wildlife Conservation Society Health Program

    In the last few decades, it has become increasingly evident that conservation, our own health, and the health of wild and domestic animals are all inextricably linked. A single pathogen can wipe out the last populations of an endangered species and, in turn, threaten the stability of local human populations. Thus there is an urgent need to simultaneously address the health of people, animals and the environment recognizing that disease poses challenges to both conservation of the planet’s biodiversity and efforts to improve the quality of human life.

    Additional Background: Global leaders in wildlife and human health issued 10 principles – The Berlin Principles – with an urgent call to governments, academia, and civil society that all sectors need to break down barriers to ensure a united effort to prevent the emergence or resurgence of diseases that threaten humans, wildlife, and livestock.

     

    Wildlife Conservation Society (WCS)

    WCS combines the power of its zoos and an aquarium in New York City and a Global Conservation Program in more than 50 countries to achieve its mission to save wildlife and wild places. WCS runs the world’s largest conservation field program, protecting more than 50 percent of Earth’s known biodiversity; in partnership with governments, Indigenous People, Local Communities, and the private sector. It’s four zoos and aquarium (the Bronx Zoo, Central Park Zoo, Queens Zoo, Prospect Park Zoo, and the New York Aquarium ) welcomes more than 3.5 million visitors each year, inspiring generations to care for nature. Founded in 1895 as the New York Zoological Society, the organization is led (as of June 1, 2023) by President and CEO Monica P. Medina. Visit: newsroom.wcs.org. Follow: @WCSNewsroom. For more information: +1 (347) 840-1242Listen to the WCS Wild Audio podcast HERE.

     

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    Wildlife Conservation Society

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  • Discovery: Nine snail species in Papua New Guinea, a biodiversity hotspot at risk.

    Discovery: Nine snail species in Papua New Guinea, a biodiversity hotspot at risk.

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    Newswise — Nine new species of carnivorous land snails have been found in the remote forests of Papua New Guinea, a biodiversity hot spot. A new study describes the species, which are so small that all nine could fit together on a U.S. nickel. They present a rare opportunity to study a group that in many other places is disappearing fast. Worldwide, mollusks account for more than 50% of all recorded extinctions since the year 1500, and many of these were land snails from Pacific islands.

    The island of New Guinea accounts for less than 1% of Earth’s land area, but it contains roughly 5% of the planet’s biodiversity and the largest intact rainforests in Australasia. Wildlife thrives within this large swath of undeveloped land, but Papua New Guinea’s old-growth forests are also highly desirable to loggers and are likely to become a conservation battleground in the future.

    “These new species of snails were found in areas that still have native vegetation and still appear to be doing well, but they could easily become endangered if things change,” said John Slapcinsky, lead author of the paper and manager of the Florida Museum’s invertebrate zoology collection.

    To reach Papua New Guinea’s isolated forests, researchers had to travel on foot over steep mountains, sometimes using fallen trees to cross crevices that were more than 100 feet deep. There are few roads in the country, which historically posed a challenge to scientists interested in researching the region but has also shielded native plants and animals from human disturbance and habitat destruction.

    Slapcinsky took nine trips to Papua New Guinea between 2002 and 2012, each time staying for at least a month to comb through the soil and fallen leaves. He ultimately collected more than 19,000 snails from over 200 sites.

    Only 31% of the snail species he surveyed had been previously documented, a sign of Papua New Guinea’s high biodiversity and low levels of sampling. But the snails are also exceptionally hard to find because of their small size, pickiness about their habitats and limited distribution. Nearly all of them are restricted to a single island or mountain.

    The newly named snails have tightly coiled, Frisbee-shaped shells in various shades of brown and tan, some with attractive gold or brown flamelike bands.  One of the new species, Torresiropa paterivolans, was named for its resemblance to flying saucers (in Latin, “patera” means “saucer,” and “volans” means “flying”).

    All nine species have dagger-shaped teeth on their radula, which is characteristic of predatory snails. Just what they’re eating, Slapcinsky said, is a mystery, since the snails did not eat anything under observation. Still, the shape of the teeth, combined with the fact that other species in the same family — Rhytididae — are predators, suggests that these newly discovered snails do eat meat.

    There is not yet enough data to know the conservation status of the new species, but it is a promising sign that their habitat has not yet been dramatically altered by human activity.

    Slapcinsky contrasted this with the Hawaiian Islands, where native snails are at imminent risk of extinction. He works with a team at the Bishop Museum in Honolulu that collaborates with the state and federal government on captive breeding programs for native snail colonies, many of which harbor the last members of their species. They also provide native snails for fenced-in areas, known as exclosures, where predators have been removed and the native forest has been replanted. These are expensive programs that Papua New Guinea still has the chance to avoid, Slapcinsky said, by slowing deforestation and preventing the introduction of non-native predators before it becomes a more serious problem.

    Snails are highly vulnerable to habitat disturbances because they cannot easily travel long distances and are usually adapted only to the environment in their immediate vicinity. “When these habitats are threatened, snails are often out of luck, since they can’t go anywhere,” Slapcinsky said.

    Many past discoveries of new snail species, especially on Pacific islands, have come after it was too late to save them. Scientists did not know that many snails lived on Easter Island, which was completely deforested centuries ago, until examining fossil deposits. But species on the island of New Guinea can still be saved if the forest is saved. The newly named snails provide a rare glimpse at an ecosystem that remains largely intact, and there are surely many similar discoveries yet to be made.

    “We don’t know everything that’s out there,” Slapcinsky said. “Most people may not realize how poorly known most of the invertebrates are, even though 95 to 99% of all animals are invertebrates. You can go to a place, look around for a few months and find all sorts of things that haven’t been described before.”

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    Florida Museum of Natural History

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  • Animal science student finds new passion working at swine center

    Animal science student finds new passion working at swine center

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    Newswise — What started with an eagerness for a hands-on learning experience in the Department of Animal Science in the Texas A&M College of Agriculture and Life Sciences ended with a new passion and opportunity for Carlie Rogers ’24, a first-generation college student from Diana.

    In April 2021, Rogers began a student worker position at the department’s swine center unit and now her sights are set on a career as a sow farm manager.

    Rogers is no stranger to the livestock industry. She grew up around livestock and companion animals and wanted to become a veterinarian. But after realizing the endless opportunities available in the animal science field, Rogers shifted her perspective on a career path.

    This shift led her to the swine center, an animal unit located on the grounds of the O.D. Butler Jr. Animal Science Teaching, Research and Extension Complex, a 580-acre center near the main Texas A&M campus in College Station comprised of five unique facilities supporting various areas in animal agriculture.

    Even though she had no prior experience working with swine, her agricultural background made her want to grow in a new area of animal agriculture. As a student worker, Rogers helped with the day-to-day operations of feeding and general care of swine, gaining a wealth of experience to support her in a future career in the swine industry.

    “I was interested in this opportunity because I wanted to learn from hands-on experiences and make connections with animal science faculty and industry stakeholders,” Rogers said.

    Immersive learning experience

    One of the best opportunities for students to directly apply the knowledge and skills learned in their animal science courses is to work at a department animal unit, said Jeffrey Wiegert, Ph.D., instructional assistant professor and Texas A&M AgriLife Extension Service swine specialist, Bryan-College Station.

    “Immersing in the day-to-day aspects of animal care exposes our student workers to thought-provoking challenges and realities of animal husbandry that are difficult to recreate in a classroom setting,” Wiegert said.

    Beyond putting their knowledge to practice while working at an animal unit, students are introduced to potential career paths from both the production and research sides of the industry. Wiegert recruits student workers from the swine center for research projects before opening the opportunity to others because the student workers are already familiar with the farm and how the animals are managed.

    “Our student workers gain a broader and deeper learning experience because they’re the ones at the farm with the animals really living it,” Wiegert said. “This is perhaps most valuable for the students who did not grow up around production agriculture or showing livestock, but who have a strong interest in science and an intense motivation to do something within the field.”

    A typical work shift includes keeping the pens and overall facility clean, feeding the animals, monitoring health and recording any observations on a daily log, Rogers said. If treatments are needed, Rogers helps administer the treatment and records the information. Other tasks involve moving pigs as needed and assisting with heat checking, artificial insemination, ultrasound for pregnancy diagnosis and piglet processing.

    “I had to go back to the basics and learn new terminology, as well as remember the techniques that were taught in the introduction classes,” Rogers said. “I also established a routine for my job responsibilities that helped ensure that every animal was well cared for.”

    Rogers said Wiegert, other student workers and the swine center manager warmly welcomed her and graciously acclimated her into the role.

    “I am thankful for all of the people I have met and everything I learned from them,” she said. “They truly made this job enjoyable. Never in a million years would I have imagined that I would have this experience and connection at a large university.”

    Strong work ethic and passion

    Wiegert said Rogers showed her intelligence, dependability, strong communication skills and a dedication to doing the right thing on the farm, which quickly earned his trust.

    “Carlie’s best attribute is that she genuinely cares for the pigs,” he said. “She always went above and beyond to ensure the animals were healthy and comfortable because she cares.”

    Rogers fed and checked the pigs before her 8 a.m. classes and returned later in the day between classes to complete other chores. During the summer, Rogers arrived at the farm at dawn to help breed sows before it became too hot. When the sows gave birth, she routinely checked the sows and piglets into the night hours and over the weekends.

    Much of the work was routine and necessary, but Rogers found a sense of accomplishment and purpose she believes will resonate beyond her time at the center. 

    “I realized that, through my work at the swine center, I was making contributions that directly benefitted the pork industry,” she said.

    Outlook for the future

    Rogers graduated with a bachelor’s degree in animal science on Dec. 14, and has multiple opportunities to continue down a path in swine production.

    Her experience working at the swine center shaped her future career aspirations and provided her with both technical knowledge and leadership skills that will benefit her in any role she decides to pursue. On the technical side, Rogers said she gained resources and knowledge to handle management responsibilities and feels confident that the lessons learned can be applied to other species.

    In addition, Rogers said she learned about the importance of working as a team and how to care for people.

    “It takes a team of good people to make a system work,” Rogers said. “As a leader, it is important to make sure everyone working with you is heard and cared for. We were one big work family that understood each other, and I will miss everyone.”

    Wiegert said it won’t be the same at the swine center without Rogers, but he knows the next students to take advantage of this learning experience will also deeply care for the animals. The experience will open doors for them in more ways than one.

    “Students, like Carlie, will learn about the dedication pig producers have for their animals and how we use science to improve pig health and welfare to increase the sustainability and profitability of pork production,” Wiegert said. “This knowledge will help our graduates apply science similarly to their chosen fields, in addition to becoming educated consumers who are lifelong advocates of animal agriculture.”

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    Would you like more information from Texas A&M AgriLife?

    Visit AgriLife Today, the news hub for Texas A&M AgriLife, which brings together a college and four state agencies focused on agriculture and life sciences within The Texas A&M University System, or sign up for our Texas A&M AgriLife E-Newsletter.

    For more resources including photo repository, logo downloads and style guidelines, please visit the Resources for Press and Media.

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    Texas A&M AgriLife

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  • Science Is the Best (Local, Regional, National, Global) Policy

    Science Is the Best (Local, Regional, National, Global) Policy

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    About a decade ago, BRI hosted a Bio Blitz at our River Point bird monitoring station in Falmouth, Maine.

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    Biodiversity Research Institute (BRI)

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  • Science Outside the Box

    Science Outside the Box

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    BYLINE: By Sarah Dodgin, Ecological Analyst, BRI

    Newswise — Neon green hoods, turquoise bellies, ornate crowns—Neotropical birds come in all shapes, sizes, and colors. Combined with unique patterns, textures, and song, they either blend in or stand out in thick jungles filled with hundreds of other species competing for the same or similar resources.

    When the first European explorers discovered Central and South America and the West Indies, they called this land the New World Tropics, a region known today as the Neotropics. Here in the dense rain forests of the Amazon, you would not suspect that many of the vibrant and charismatic birds that inhabit these remote areas are regularly exposed to sublethal amounts of mercury. In this seemingly pristine part of the world, how does mercury find its way into these birds?

    From affordable common goods to expensive investments, so many of our daily decisions seem inconsequential. But as our awareness grows, we are forced to think before we make a transaction and to ask ourselves a few questions: Where did this product come from? What industry is this tied to? And who, be it person or animal, is paying the price for my purchase?

    Many people have some understanding of the ethical dilemma associated with diamond mining. Conflict free, responsibly mined, and ethically sourced are all things we are urged to deliberate when making a selection of this precious gem. But what about gold? It turns out there are similar social and environmental considerations when picking out a pair of hoops. According to the World Gold Council and the World Bank, 15 to 20 million people make artisanal small-scale gold mining (ASGM) their primary source of income. Unlike large-scale gold mining, ASGM takes place outside of formal legal and economic structures, and although the operation itself is small in scale, its prevalence around the world looms large. In addition to labor rights and safety concerns for miners, another metal involved in the gold extraction process poses a threat to entire ecosystems.

    Mercury, a dense and silvery fluid, is the only metal in a liquid state at standard room temperature and pressure. Although mercury naturally occurs in small quantities in its elemental form and is usually contained deep in the Earth’s crust, the United Nations Environment Programme found that industrial activities such as ASGM, fossil fuel combustion, and waste incineration increase the amount of mercury released into the environment. Furthermore, mercury rapidly becomes a global issue because of its ability to mobilize far from the source of emission, contaminating soils, waterways, and the atmosphere. Particularly deleterious is the biomagnification (the ability for toxin levels to increase to successively higher concentrations in a food web) property of mercury when transformed to its organic form methylmercury. If exposed under the right conditions, mammals, birds, and fish suffer from behavioral, immunological, neurological, physiological, and reproductive impairment. Yet, there is a lack of Information on how mercury contamination occurs in the Neotropics, and the prevalence of mercury in birds across this region.

    To remedy this important knowledge gap, Chris Sayers, an associate research biologist at BRI and a Ph.D. student at UCLA, embarked on a mission to collaborate with more than 30 researchers from ten organizations throughout the Americas, including BRI. By examining 13 years of data comprising more than 2,000 samples from 322 neotropical bird species,

    documenting bird blood and feather samples from every site and habitat type surveyed in eight countries across Central America, South America, and the West Indies. “It wasn’t surprising to find these samples contained some amount of mercury because mercury is a naturally occurring, persistent, and globally distributed element,” says Sayers. “What is startling, however, is the elevated concentrations that we detected.”

    Beyond identifying mercury-emitting sources and mercury contamination hotspots through blood and feather sampling, determining the risk of mercury exposure in Neotropical birds was the study’s most notable outcome. Sayers found that risk was most strongly determined by four variables: diet, habitat, proximity to ASGM, and seasonal rainfall.

    Without the cooperation of dozens of researchers to create a database of thousands of mercury concentrations, these findings would not be possible. That’s why BRI’s Tropical Research for Avian Conservation and Ecotoxicology (TRACE) Initiative was created. TRACE serves as an inclusive and equitable data-sharing platform, documenting mercury exposure in birds. More broadly, TRACE gives scientists the ability to uncover the greater implications of mercury pollution to global biodiversity loss and human health. Through continued research and international collaboration, birds will remain as bioindicators of mercury pollution to create positive impacts for communities threatened by exposure globally.

    A small percentage of Neotropical birds are migratory. You might not realize it, but chances are you have seen, or know the names of some species. Common birds you may find in your backyard during the summer include warblers, swallows, vireos, and hummingbirds. This time of year, while we are watching the snow fall, they are keeping warm in countries such as Brazil and Costa Rica. But in order to keep them coming back year after year, regulators must curb mercury pollution in all industries, especially within artisanal small-scale gold mining.

    As consumers, it is our job to decide where our values lie this holiday season (and all year long). Will global biodiversity be one of them?

     

    More stories on https://briwildlife.org/bri-blog/.

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    Biodiversity Research Institute (BRI)

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  • Inside the Matrix: Nanoscale Patterns Revealed Within Model Research Organism

    Inside the Matrix: Nanoscale Patterns Revealed Within Model Research Organism

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    BYLINE: Mario Aguilera

    Newswise — Species throughout the animal kingdom feature vital interfaces between the outermost layers of their bodies and the environment. Intricate microscopic structures—featured on the outer skin layers of humans, as one example—are known to assemble in matrix patterns.

    But how these complex structures, known as apical extracellular matrices (aECMs) are assembled into elaborately woven architectures has remained an elusive question.

    Now, following years of research and the power of a technologically advanced instrument, University of California San Diego scientists have unraveled the underpinnings of such matrices in a tiny nematode. The roundworm Caenorhabditis elegans has been studied extensively for decades due to its transparent structure that allows researchers to peer inside its body and examine its skin.

    Described in the journal Nature Communications, School of Biological Sciences researchers have now deciphered the assemblage of aECM patterns in roundworms at the nanoscale. A powerful, super-resolution microscope helped reveal previously unseen patterns related to columns, known as struts, that are key to the proper development and functioning of aECMs.

    “Struts are like tiny pillars that connect the different layers of the matrix and serve as a type of scaffolding,” said Andrew Chisholm, a professor in the School of Biological Sciences and the paper’s senior author.

    Although roundworms serve as a model organism for laboratory studies due to their simple, transparent bodies, below the surface they feature intricate architectures. They also have nearly 20,000 genes, not unlike the number of human genes, and therefore provide lessons on structure and function of more advanced organisms.

    Focusing on the roundworm exoskeleton known as the cuticle, the researchers found that defects in struts result in unnatural layer swelling, or “blistering.” Within the cuticle layer, the research study focused on collagens, which are the most abundant family of proteins in our bodies and help keep bodily materials conjoined.

    “The struts hold the critical layers together,” said Chisholm. “Without them, the layers separate and cause disorders such as blistering. In blistering mutants you don’t see any struts.”

    Conventional laboratory instruments had previously imaged struts without detail, often resulting in undefined blobs. But through Biological Sciences Assistant Professor Andreas Ernst’s laboratory they accessed advanced instrumentation—known as 3D-structured illumination super resolution microscopy (3D-SIM)—which put the struts into stunning focus and allowed their functions to be more easily defined. The researchers were then able to solve the nanoscale organization of struts and previously undocumented levels of patterning in the cuticle layer.

    “We could see exactly where these proteins were going in the matrix,” said Chisholm. “This is potentially a paradigm for how the matrix assembles into very complex structures and very intricate patterning.”

    The two first authors, Jennifer Adams (senior research associate) and Murugesan Pooranachithra (postdoctoral fellow), contributed equally to the paper. Other coauthors are Erin Jyo, Sherry Li Zheng, Alexandr Goncharov, Jennifer Crew, James Kramer, Professor of Neurobiology Yishi Jin, Assistant Professor of Cell and Developmental Biology Andreas Ernst and Andrew Chisholm.

    Sherry Zheng was a UC San Diego Triton Research and Experiential Learning Scholar and received the Gabriele Wienhausen Biological Sciences Scholarship. Funding for the research was provided by the Howard Hughes Medical Institute; the National Institutes of Health  (R35 GM142433, R01 GM054657 and R35 GM134970).

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    University of California San Diego

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  • Bird feeding may give humans something to chirp about

    Bird feeding may give humans something to chirp about

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    BYLINE: Travis Williams

    Newswise — Ashley Dayer hopes to peck away at the notion that bird feeding is simply for the birds.

    An associate professor in the Department of Fish and Wildlife Conservation at Virginia Tech, Dayer is the lead author of an article published in People and Nature that argues not only for the acknowledgment of the activity’s benefit to humans, but that it should play a role in public guidance and policy.

    “Wildlife agencies and others making decisions on managing bird feeding need to be considering not only what the science is behind what’s going on with birds, but also the science behind what’s going on with people,” Dayer said.

    The article also encourages additional research to better understand how human well-being is impacted by regularly feeding birds, and Dayer and a team of researchers both in and outside of Virginia Tech are leading the way. The group is conducting what is perhaps the first large-scale bird feeding research that also incorporates observing humans.

    “People are not only reporting what they see at their bird feeders, but also their emotional responses to it,” Dayer said. “It’s pretty fun because most citizen science projects focus just on the natural or physical science, but we’re now able to look at the human piece of it.”

    Funded recently as part of a more than $1.5 million National Science Foundation grant led by Dayer and Dana Hawley, professor of biological sciences, the four-year project aims to engage more than 10,000 bird feeders across the United States.

    Other collaborators on the article and project include

    • Christy Pototsky, a graduate student studying fish and wildlife conservation at Virginia Tech
    • Richard Hall, associate professor at the University of Georgia
    • Alia Dietsch, associate professor at Ohio State University
    • Tina Phillips, David Bonter, Emma Greig, and Wesley Hochachka of the Cornell Lab of Ornithology

    Dayer said interest in the topic began in 2021, when the researchers began to notice state agencies advising people to stop feeding birds in response to various avian disease outbreaks. After looking into it, they found that 23 states had made such recommendations without evidence it would decrease disease spread, with varying levels of pushback, and with no real method of gauging compliance, much less its impact on people.

    The new project is an extension of the work Dayer and Hawley began about six years ago with the help of a joint seed grant from the Global Change Center of the Fralin Life Sciences Institute and the Institute for Society, Culture, and the Environment.

    Hawley said the lack of information about humans related to bird feeing was something she’d not previously considered, and she found it a strong motivator for this project.

    “In all my years of studying how bird feeding impacts wild birds, I didn’t give much thought to how it can also impact the people that spend their time and money feeding and watching birds,” Hawley said. “I get calls every year from people who see a sick bird at their feeder and want to know how they can help prevent disease spread. All in all, this made me wonder about how policy decisions that aim to minimize disease spread can inadvertently impact the people who feed the birds.”

    To help find those answers, the research team will utilize Project FeederWatch’s existing network of bird enthusiasts. Operated by the Cornell Lab of Ornithology and Birds Canada, FeederWatch has tasked people with asks participants to observe and report what they see at their feeders from November to April for the past 37 years.

    “FeederWatch is such a versatile data set even though, at its core, it is based on simple bird counts,” said Emma Greig, co-author and project leader for FeederWatch. “When you overlay information about behavior, disease, habitat, and climate change with those bird counts, we can get amazing insights into ecology and evolution.”

    During this project, FeederWatch participants also will be asked to observe their own well-being. Dayer said about 8,000 submissions came in in from the first week of this season alone.

    Such passion for birds is something Dayer understands very well. She said her mother always made sure they had bird feeders outside their family’s home, and when she became an “empty nester,” the birds became almost like children.

    “She’ll go on vacation and cut the vacation short because she needs to go home and feed her birds,” Dayer said. “So I’ve lived with someone who was really into bird feeding and have seen how important it can be to them.”

    But Dayer believes the positive impact of bird feeding isn’t limited to enthusiasts and is important in proving one of the most widely accessible connection to wildlife.

    “People in urban areas can feed birds. People with just a deck can feed birds. People with a wide range of physical abilities can feed birds. So it’s just a great way to keep that human connection to wildlife,” Dayer said.

    Hawley agreed with that sentiment, and said she hopes their work helps advance policies that will foster both health and healthy relationships.

    “In a world where so many of us live in cities or suburbs, having birds visit feeders in our yards or on our balconies is one of the only ways we get to connect daily with wildlife. But people want to be able to feed birds in ways that keep wild bird populations healthy and thriving,” Hawley said. “Our work will ideally help us develop guidelines for bird feeding that minimize risk to wild birds and maximize the benefits to the people that feed them.”

    The Department of Fish and Wildlife Conservation is in the College of Natural Resources and Environment. The Department of Biological Sciences is in the College of Science.
     

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  • Fossil plant revealed as a baby turtle fossil.

    Fossil plant revealed as a baby turtle fossil.

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    Newswise — From the 1950s to the 1970s, a Colombian priest named Padre Gustavo Huertas collected rocks and fossils near a town called Villa de Levya. Two of the specimens he found were small, round rocks patterned with lines that looked like leaves; he classified them as a type of fossil plant. But in a new study, published in the journal Palaeontologia Electronica, researchers re-examined these “plant” fossils and found that they weren’t plants at all: they were the fossilized remains of baby turtles.

    “It was truly surprising to find these fossils,” says Héctor Palma-Castro, a paleobotany student at the Universidad Nacional de Colombia.

    The plants in question had been described by Huertas in 2003 as Sphenophyllum colombianum. The fossils come from Early Cretaceous rocks, between 132 and 113 million years ago, during the dinosaurs’ era. Fossils of Sphenophyllum colombianum were surprising at this time and place— the other known members of the genus Sphenophyllum died out more than 100 million years prior. The plants’a ge and locality piqued the interest of Fabiany Herrera, the Negaunee assistant curator of fossil plants at the Field Museum in Chicago, and his student, Palma-Castro.

    “We went to the fossil collection at the Universidad Nacional de Colombia in Bogotá and started looking at the plants, and as soon as we photographed them, we thought, ‘this is weird,’” says Herrera, who has been collecting Early Cretaceous plants from northwestern South America, an area of the world with little paleobotanical work.

    At first glance, the fossils, about 2 inches in diameter, looked like rounded nodules containing the preserved leaves of the plant Sphenophyllum. But Herrera and Palma-Castro noticed key features that weren’t quite right.

    “We spent days searching through wooden cabinets for fossil plants. When we finally found this fossil, deciphering the shape and margin of the leaf proved challenging,” says Palma-Castro.

    “When you look at it in detail, the lines seen on the fossils don’t look like the veins of a plant— I was positive that it was most likely bone,” says Herrera. So he reached out to an old colleague of his, Edwin-Alberto Cadena.

    “They sent me the photos, and I said, “This definitely looks like a carapace’— the bony upper shell of a turtle,” says Cadena, a paleontologist who focuses on turtles and other vertebrates at the Universidad del Rosario in Bogotá. When he saw the scale of the photos, Cadena recalls, “I said, ‘Well, this is remarkable, because this is not only a turtle, but it’s also a hatchling specimen, it’s very, very small.”

    Cadena and his student, Diego Cómbita-Romero of the Universidad Nacional de Colombia, further examined the specimens, comparing them with the shells of both fossil and modern turtles. “When we saw the specimen for the first time I was astonished, because the fossil was missing the typical marks on the outside of a turtle’s shell,” says Cómbita-Romero. It was a little bit concave, like a bowl. At that moment we realized that the visible part of the fossil was the other side of the carapace, we were looking at the part of the shell that is inside the turtle.”

    Details in the turtle’s bones helped the researchers estimate how old it was at death. “Turtle growth rates and sizes vary,” says Cómbita-Romero, so the team looked at features like the thickness of its carapace and the spots where its ribs were knitting together into solid bone. “This is a feature uncommon in hatchlings but observed in juveniles. All this information suggests that the turtle likely died with a slightly developed carapace, between 0 to 1 years old, in a post-hatchling stage,” he says.

    “This is actually really rare to find hatchlings of fossil turtles in general,” says Cadena. “When the turtles are very young, the bones in their shells are very thin, so they can be easily destroyed.”

    The researchers say that the rarity of fossilized baby turtles makes their discovery an important one. “These turtles were likely relatives of other Cretaceous species that were up to fifteen feet long, but we don’t know much about how they actually grew to such giant sizes,” says Cadena.

    The researchers don’t fault Padre Huertas for his mistake— the preserved shells really do resemble many fossil plants. But the features that Huertas thought were leaves and stems are actually the modified rib bones and vertebrae that make up a turtle’s shell. Cómbita-Romero and Palma-Castro nicknamed the specimens as “Turtwig,” after a Pokémon that’s half-turtle, half-plant.

    “In the Pokémon universe, you encounter the concept of combining two or more elements, such as animals, machines, plants, etc. So, when you have a fossil initially classified as a plant that turns out to be a baby turtle, a few Pokémon immediately come to mind. In this case, Turtwig, a baby turtle with a leaf attached to its head,” says Palma-Castro.” In paleontology, your imagination and capacity to be amazed are always put to the test. Discoveries like these are truly special because they not only expand our knowledge about the past but also open a window to the diverse possibilities of what we can uncover.”

    The scientists also note the importance of these fossils in the larger scheme of Colombian paleontology. “We resolved a small paleobotanical mystery, but more importantly, this study shows the need to re-study historical collections in Colombia. The Early Cretaceous is a critical time in land plant evolution, particularly for flowering plants and gymnosperms. Our future job is to discover the forests that grew in this part of the world,” says Herrera.

    This project was supported by the National Geographic Society, grant (EC-96755R-22) Discovering Early Cretaceous Floras from Northern South America & the Negaunee Integrative Research Center, Field Museum.

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  • Skunks’ warning stripes less prominent where predators are sparse, study finds

    Skunks’ warning stripes less prominent where predators are sparse, study finds

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    Newswise — Striped skunks are less likely to evolve with their famous and white markings where the threat of predation from mammals is low, scientists from the University of Bristol, Montana and Long Beach, California have discovered.

    Skunks’ iconic black and white colouration signals its toxic anal spray. However some skunks show very varied fur colour ranging from all black to thin or thick black and white bands to all white individuals. Variation is huge across the North American continent.

    Findings published today in Evolution, suggest that this is a result of relaxed selection, when environmental change eliminates or weakens the selection of a normally important trait – in this case black and white pelage.   

    Prof Tim Caro from Bristol’s School of Biological Sciences explained: “Warning coloration is an antipredator defence whereby a conspicuous signal advertises the ability of prey to escape predation, often because it is toxic or has spines or is pugnacious.”

    “Usually predators have to learn the significance of this signal and so it is predicted that warning colouration will look very similar across prey individuals of the same, as well as perhaps different, prey species to be an effective education tool. Yet some warningly coloured prey show rather different advertisements even within the same species.”

    Researcher Hannah Walker from the University of Montana documented the distribution of these different pelage colours across their range in North America using museum specimens. She plotted these against a menu of variables that the team thought might drive this variation in coloration.

    The team found that in locations in which skunks overlapped with rather few mammalian predators that might be capable of killing them, fur colour was varied even within the same litter.

    Where there were many species of predators that were a danger to them, they showed little variation.

    The team also examined owl and raptorial predators however while the effects were the same, they were not as evident. This is perhaps because birds have a poorer sense of smell and are less deterred by smelly anal defences. 

    “Our results indicate that relaxed predation pressure is key to warning signal variation in this species, whereas stronger pressure leads to signal conformity and stronger signals,” said Professor Caro.

    “We now know why not all skunks look alike, and perhaps why members of other warningly coloured species look different from each other.”

    Now the team plan to see if this occurs across other skunk species whose geographic ranges overlap in North America.

    Prof Caro concluded: “If relaxed selection operates within species, it should do so across prey species too. More broadly, this study provides another brick in the wall of explaining the evolution of coloration in nature.”

     

    Paper:

    ‘Predation risk drives aposematic signal conformity’ by Hannah Walker, Tim Caro et al in Evolution

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  • These bats use their penis as an “arm” during sex but not for penetration

    These bats use their penis as an “arm” during sex but not for penetration

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    Newswise — Mammals usually mate via penetrative sex, but researchers report November 20 in the journal Current Biology that a species of bat, the serotine bat, (Eptesicus serotinus) mates without penetration. This is the first time non-penetrative sex has been documented in a mammal. The bats’ penises are around seven times longer than their partners’ vaginas and have a “heart-shaped” head that is seven times wider than the vaginal opening. Both the penises’ size and shape would make penetration post-erection impossible, and the researchers show that, rather than functioning as a penetrative organ, the bats use their oversized penises like an extra arm to push the female’s tail sheath out of the way so that they can engage in contact mating—a behavior that resembles “cloacal kissing” in birds.

    “By chance, we had observed that these bats have disproportionately long penises, and we were always wondering ‘how does that work?’,” says first author Nicolas Fasel of the University of Lausanne. “We thought maybe it’s like in the dog where the penis engorges after penetration so that they are locked together, or alternatively maybe they just couldn’t put it inside, but that type of copulation hasn’t been reported in mammals until now.”

    Very little is known about how bats have sex, and most previous observations of bats mating have only perceived the backs of mating pairs. In this study, the researchers were able to observe the bats’ genitalia during copulation by using footage from cameras that were placed behind a grid that the bats could climb on.

    Fasel collaborated with a bat rehabilitation center in Ukraine that opportunistically filmed mating pairs and with a bat enthusiast and citizen scientist, Jan Jeucken, who filmed hours of footage of serotine bat in a church attic in the Netherlands. Altogether, the team analyzed 97 mating events—93 from the Dutch church and 4 from the Ukrainian bat rehabilitation center.

    The video recordings revealed that the bats do not engage in penetrative sex. The researchers did not observe penetration at any point during the recorded mating events and noted that the erectile tissues of the penis were enlarged before they made contact with the vulva. During mating, the male bats grasped their partners by the nape and moved their pelvises (and fully erect penises) in a probing fashion until they made contact with the female’s vulva, at which point they remained still and held the females in a long embrace. On average, these interactions lasted less than 53 minutes, but the longest event extended to 12.7 hours. Following copulation, the researchers observed that the female bats’ abdomens appeared wet, suggesting the presence of semen, but further research is needed to confirm that sperm was transferred during these putative mating events.

    The researchers also characterized the morphology of serotine bat genitalia by measuring the erect penises of live bats that were captured as part of other research studies (serotine and other vesper bats are conveniently known to get erections under anesthesia) and by performing necropsies on bats that died at bat rehabilitation centers. Their measurements showed that, when erect, serotine bat penises are around seven times longer and seven times wider than serotine bat vaginas, and about a fifth as long as the bats’ head-body length. The bats also have unusually long cervixes, which could help female bats select and store sperm.

    The researchers speculate that the bats may have evolved their oversized penises in order to push aside the female bats’ tail membranes, which females may use to avoid sex. “Bats use their tail membranes for flying and to capture the insects, and female bats also use them to cover their lower parts and protect themselves from males,” says Fasel, “but the males can then use these big penises to overcome the tail membrane and reach the vulva.”

    Next, the researchers plan to study bat mating behavior in more natural contexts, and they are also investigating penis morphology and mating behavior in other bat species. “We are trying to develop a bat porn box, which will be like an aquarium with cameras everywhere,” says Fasel.

     

    ###

    This research was supported by the National Science Centre of Poland, the Swiss National Science Foundation, and the Oleksandr Feldman Foundation.

    Current Biology, Fasel et al., “Mating without intromission in a bat, a novel copulatory pattern in mammals” https://cell.com/current-biology/fulltext/S0960-9822(23)01304-0

    Current Biology (@CurrentBiology), published by Cell Press, is a bimonthly journal that features papers across all areas of biology. Current Biology strives to foster communication across fields of biology, both by publishing important findings of general interest and through highly accessible front matter for non-specialists. Visit: http://www.cell.com/current-biology. To receive Cell Press media alerts, contact [email protected].

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  • New species with “hieroglyphic” pattern discovered among sand dunes

    New species with “hieroglyphic” pattern discovered among sand dunes

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    A brand new lizard species with a hieroglyphic pattern on its back has been discovered among the sand dunes in eastern Iran.

    The discovery, which was detailed in a study in the journal Zootaxa on November 10, was made back in 2010 in the South Khorasan province of the desert, while researchers were conducting a survey for local reptiles and amphibians.

    The researchers found a total of 10 strange-looking lizards in the sand dunes, all with an unusual pattern on their skin. They discovered that it was actually an entirely new species, now named Eremias graphica, or the “hieroglyphic racerunner lizard.”

    The new species is named using the Greek word “graphikos,” according to the study, as reported by the Miami Herald. This translates to either “drawn” or “written,” and was used because of the lizard’s strange pattern which resembles hieroglyphs.

    A photo shows the new lizard species found in the sand dunes of Iran. A closer look at the creature shows a strange pattern on its back.
    Eskandar Rasegar-Pouyani, Valentina Orlova, Khosrow Rajabizadeh, Hossein Nabizadeh, Nikolay Poyarkov, Daniel Melnikov and Roman Nazarov

    Hieroglyphs are generally associated with Ancient Egypt, though other forms of writing also exited at the time.

    The researchers found that most of the lizards were about 7 inches long and were easily disguised in the sand dunes due to their sandy coloring, according to the study.

    The researchers, who are from multiple organizations from across Russia and Iran, analyzed 93 genetic samples from the lizards in the desert.

    “We hypothesize that the diversification of the Eremias fasciata species complex was largely influenced by the fragmentation of sand massifs in the region,” an abstract from the study read. “This same hypothesis has been used to explain the high level of endemism among the sand-dwelling species of reptiles along the Iranian Plateau in the same area. The two new species described herein can be distinguished from other congeneric species by their phylogenetic position and a combination of morphological characters. We use these data to discuss the taxonomy of Eremias based on morphology, habitat choice, and genetic data.”

    The study noted that the lizards can mainly be found scuttling around the vegetation found in the sand dunes, the Miami Herald reported. They can also be found burrowing for shade and shelter. The researchers reported that they typically eat insects.

    Closer analysis of the creature showed that it was most active during some hours in the morning, and evening. During the rest of the day, it tends to hide under the bushes of the sand dunes.

    So far, the new species has only been found near one road near the city of Tabas, in central-eastern Iran.