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Behavioral Science

Echidna Pseudo-Pouch Microbiome Shifts During Lactation Helps Young Thrive

Research shows microbial communities in echidna pseudo-pouches undergo dramatic changes while the animal is lactating, which could help in creating an environment for their young, known as puggles, to thrive.

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Echidnas, the only mammals that lay eggs, have an unusual reproductive system that includes a pseudo-pouch where their young, called puggles, grow and develop during lactation. Researchers from the University of Adelaide have made a fascinating discovery about the microbiome in these pseudo-pouches, which changes significantly while the mother is nursing her young.

The study, published in FEMS Microbiology Ecology, reveals that the microbial communities in echidna pseudo-pouches undergo dramatic changes during lactation, creating an environment that’s conducive to the health and well-being of their puggles. This is particularly important since puggles hatch at a very early developmental stage, lacking a functional immune system.

“We know that the reproductive microbiome is crucial for infant health in many species, including humans,” says Isabella Wilson, lead researcher on the study. “However, little was known about how it functions in egg-laying monotremes like echidnas.”

One of the key findings of this research is that during lactation, the pseudo-pouch microbial communities show significant differences in composition compared to samples taken outside of breeding season or during courtship and mating. This suggests that the echidna pseudo-pouch environment changes during lactation to accommodate young that lack a functional adaptive immune system.

The way puggles suckle may contribute to this shift in microbes. Unlike other species, echidnas don’t have nipples; instead, their young rub their beaks against a part of the pseudo-pouch called the milk patch, causing milk to come out of the skin, similar to a sweat or oil gland.

Compounds within the milk and from the skin probably contribute to the changes seen in the pseudo-pouch microbiota during lactation. This study highlights the importance of understanding these unique reproductive dynamics for conservation efforts and breeding programs for echidnas.

The research also sheds light on previous findings that showed big differences in the gut microbiome between echidnas in zoos and those in the wild. Surprisingly, no major difference was found in the pseudo-pouch microbiota between zoo-managed and wild animals. This suggests that the milk, rather than external environmental factors like captivity, is what primarily shapes the bacterial landscape of the pseudo-pouch.

For conservation efforts and breeding programs, it’s essential to learn more about the bacteria found in echidna pseudo-pouches and how they affect echidna health. This knowledge will help ensure the well-being of these unique animals and their young, ultimately contributing to the preservation of this fascinating species.

Behavioral Science

Satellite tracking of 12,000 marine animals reveals ocean giants are in trouble

A massive global collaboration has tracked over 12,000 marine animals from whales to turtles to create one of the most detailed movement maps of ocean giants ever assembled. The project, MegaMove, highlights how animal migrations intersect with fishing, shipping, and pollution, revealing alarming gaps in current ocean protections. Even if 30% of the oceans were protected, most critical habitats would still be exposed to threats.

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The world’s oceans are home to an incredible array of marine life, from massive blue whales to tiny plankton. However, many of these ocean giants are facing significant threats, including overfishing, pollution, and climate change. A recent study has shed new light on the plight of these marine animals, using satellite tracking data to pinpoint where they need the most protection.

Led by Ana Sequeira of Australian National University and supported by the United Nations, the research project, called MegaMove, brought together nearly 400 scientists from over 50 countries. The team used biologging data collected from satellite tags to inform a new blueprint for ocean conservation.

“This is one of the largest marine tracking data sets ever assembled,” said Francesco Ferretti, a marine ecologist at Virginia Tech who contributed to the study. “It’s not just about drawing lines on a map. We need to understand animal behavior and overlap that with human activity to find the best solutions.”

The research revealed some startling insights into the migratory patterns of these ocean giants. For example, Virginia’s coastline is part of a major migratory corridor for marine species, including sharks, which play a critical role in maintaining healthy marine ecosystems.

“Sharks, for example, play a critical role in maintaining healthy marine ecosystems, which in turn support fisheries and recreation,” Ferretti said. “What happens to apex predators can ripple across the food web and impact local economies.”

Past collapses of shellfish fisheries in North Carolina and impacts on seagrasses meadows have shown how predator loss can shift entire ecosystems.

The MegaMove project aimed to inform the United Nations’ 30×30 target: a global goal to protect 30 percent of the world’s oceans by 2030. However, the findings show that even if all 30 percent of protected areas were perfectly placed, it wouldn’t be enough.

“Sixty percent of the tracked animals’ critical habitats would be still outside these zones,” Ferretti said. “In addition to protected areas, we need targeted mitigation, changing fishing practices, rerouting shipping lanes, and reducing pollution.”

The project highlights the importance of collaboration and global science in addressing these challenges. Virginia Tech’s participation reflects a broader push to contribute to international, data-driven science.

“This project shows where the field is heading,” Ferretti said. “We’re seeing a revolution in big data approaches in marine science. Students need to be trained not only in fieldwork but in data science to meet future challenges.”

The MegaMove project can also help inspire the next generation of researchers and showcase how Virginia Tech connects local talent to worldwide impact.

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Animals

Baboons’ Social Bonds Drive Their Travel Patterns, Not Survival Strategies

Researchers have discovered that baboons walk in lines, not for safety or strategy, but simply to stay close to their friends.

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Researchers at Swansea University have made an intriguing discovery about the behavior of wild chacma baboons on South Africa’s Cape Peninsula. By using high-resolution GPS tracking, they found that these intelligent primates walk in lines not for safety or strategy, but simply to stay close to their friends.

For a long time, scientists believed that baboons structured their travel patterns, known as “progressions,” to reduce risk and optimize access to food and water. However, the new study published in Behavioral Ecology reveals that this behavior is actually driven by social bonds rather than survival strategies.

The researchers analyzed 78 travel progressions over 36 days and found that the order in which individual baboons traveled was not random. They tested four potential explanations for this phenomenon, including strategic positioning to avoid danger or gain access to resources. However, their findings show that the consistent order of baboon movement patterns is solely driven by social relationships.

According to Dr. Andrew King, Associate Professor at Swansea University, “The baboons’ consistent order isn’t about avoiding danger like we see in prey animals or for better access to food or water. Instead, it’s driven by who they’re socially bonded with. They simply move with their friends, and this produces a consistent order.”
This discovery introduces the concept of a “social spandrel.” In biology, a spandrel refers to a trait that arises not because it was directly selected for but as a side effect of something else. The researchers found that the consistent travel patterns among baboons emerge naturally from their social affiliations with each other and not as an evolved strategy for safety or success.

The study highlights the importance of strong social bonds in baboon society, which are linked to longer lives and greater reproductive success. However, this research also shows that these bonds can lead to unintended consequences, such as consistent travel patterns, which serve no specific purpose but rather as a by-product of those relationships. The findings have implications for our understanding of collective animal behavior and the potential for social spandrels in other species.

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Behavioral Science

Unlocking the Secret to Staying Cool: A Breakthrough in Thermosensory Regulation

Researchers have identified a monoacylglycerol acyltransferase-coding gene named bishu-1. It is involved in the thermal responsiveness of cool temperature-sensing neurons by regulating ionotropic receptor expression, thereby maintaining the cool temperature avoidance behaviors in Drosophila larvae.

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The human body has an incredible ability to sense changes in environmental temperatures, but have you ever wondered how insects like fruit flies can detect even slight temperature variations? A team of researchers from the Exploratory Research Center on Life and Living Systems (ExCELLS) has made a groundbreaking discovery that sheds light on this fascinating phenomenon. Their study reveals a lipid enzyme called bishu-1 plays a crucial role in maintaining cool temperature sensation and avoidance behavior in insects.

The research focused on thermal receptors, specifically ionotropic receptors (IRs), IR25a and IR21a, which are responsible for detecting cool temperatures in the dorsal organ cool cells (DOCCs) of larval fruit flies. The team discovered that bishu-1 regulates the expression level of these receptors, ensuring their proper functioning and enabling the insects to accurately sense cool temperatures.

“Bishu-1” is a Chinese word meaning “summering,” which aptly describes the escaping behavior of larvae from heat. This lipid enzyme’s role in thermosensation was unexpected, as it is primarily known for its involvement in energy storage processes in the liver or intestine.

The researchers found that bishu-1 regulates the expression of transcription factor broad, which binds to the regulatory region of the IR25a gene. This mechanism is essential for maintaining cool temperature sensation and avoidance behavior in insects. Interestingly, overexpressing broad was sufficient to rescue the bishu-1 mutant’s defects in cooling responses and cool temperature avoidance behaviors.

This study opens up new avenues for research into lipid-mediated mechanisms affecting multiple sensory processes. It also has potential implications for the discovery of treatments that can maintain thermosensation and other sensory systems in humans, promoting a better understanding of the intricate relationships between our bodies and the environment.

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