AI-designed antibodies race toward trials Scientists say they are on the cusp of turning antibodies designed by artificial intelligence into potential therapies, just a year after they debuted the first example of an entirely AI-designed antibody. Previously, the structure of antibodies proved somewhat of a black box to AI models. But new and improved models — such as an updated version of AlphaFold — have more successfully predicted the shape of flexible structures that give antibodies the specificity they need to bind to foreign molecules. Researchers at several companies now say they’ve designed ‘drug-like’ antibodies.
Scientists build a quantum computer that can repair itself using recycled atoms
Like their conventional counterparts, quantum computers can also break down. They can sometimes lose the atoms they manipulate to function, which can stop calculations dead in their tracks. But scientists have demonstrated a solution that allows a quantum computer to repair itself while it's still running.
The research team zeroed in on quantum computers that use neutral atoms (atoms with equal numbers of protons and electrons). These individual atoms are the qubits, or the basic building blocks of a quantum computer's memory. They are held in place by laser beams called optical tweezers, but the setup is not foolproof.
Occasionally, an atom slips out of its trap and disappears. When this happens mid-calculation, the whole process can grind to a halt because the computer can't function with a missing part.
In a paperpublishedin the journalPhysical Review X, the researchers detail how they solved this problem by rearranging the atoms within the machine. Instead of having all the atoms in a single crowded group, the team organized them into five distinct zones. This means that if an atom is lost in one part of the computer, the other qubits will not be affected.
The specialized zones are a "Register" for storing qubits, an "Interaction Zone" for performing calculations and a "Measurement zone" for checking errors using helper atoms known as "ancillas." There is also a "Storage Zone," a reservoir of spare atoms to replace those that are lost and a "Loading Zone' to bring in new atoms from the outside to refill the reservoir.
But the solution is even more sophisticated than that. This neutral atom-based quantum computer can detect a breakdown and fix it on the fly. When the system notices a missing qubit, it reaches into the storage zone and moves a new atom into place.
Once this atom is in position, the computer prepares it for work by resetting it to its ground state (lowest-energy state). The computer can also recycle the ancillas once they have performed their checks by resetting them in the same way.
To demonstrate that their solution works, the study authors had the computer run a repetition code, a process that checks its own work for mistakes. They ran these checks 41 times in a row, and each time, the machine successfully replaced its lost atoms without disturbing the data being processed. Without this self-repairing ability, the system would have run out of atoms after a few rounds.
J. A. Muniz et al, Repeated Ancilla Reuse for Logical Computation on a Neutral Atom Quantum Computer, Physical Review X (2025). DOI: 10.1103/v7ny-fg31
Life has a way of bouncing back, even after catastrophic events like forest fires or volcanic eruptions. While nature's resilience to natural disasters has long been recognized, not much is known about how organisms colonize brand-new habitats for the first time. A new study by a team of ecologists and planetary scientists provides glimpses into a poorly understood process.
The team conducted field research in Iceland following a series of eruptions of the Fagradalsfjall volcano, located on the southwestern tip of the island. The volcano erupted for a total of three times over the course of the study period, from 2021 until 2023. With each eruption, lava flows blanketed the tundra around the volcano, in some places even covering lava deposits from the previous year.
The lava coming out of the ground is over 2,000 degrees Fahrenheit, so obviously it is completely sterile. It's a clean slate that essentially provides a natural laboratory to understand how microbes are colonizing it.
To untangle the ecological dynamics involved in that process, the team searched for clues about where the microbes that colonize fresh lava come from. They collected samples from a variety of different potential sources, including lava that had solidified mere hours before, rainwater, and aerosols—particles floating in the air. For context, they sampled soil and rocks from surrounding areas.
The researchers then extracted DNA from these samples and used sophisticated statistical and machine learning techniques to identify the organisms present on freshly imposed lava flows, the composition of these micro-habitats and where they originated.
The work revealed that as microbes colonized the new habitat, biodiversity increased over the course of the first year following an eruption. But after the first winter, diversity "tanked', probably because the seasonal shifts in environmental conditions were selecting for a specific subset that could survive those conditions. With each subsequent winter, the analyses revealed less turnover and showed that diversity stabilized over time. With all these data, a picture began to emerge.
It appears that the first colonizers are these 'badass' microbes, for lack of a better term, the ones that can survive these initial conditions, the researchers say, "because there's not a lot of water and there's very little nutrients. Even when it rains, these rocks dry out really fast.
Over the next several months and seasonal shifts, the study revealed, the microbial community begins to stabilize, as more microbes are added with rainwater and "moved in" from adjacent areas.
A major finding of the study pointed to rainwater playing a critical role in shaping microbial communities on freshly deposited lava, according to the researchers.
Early on, it appears colonizers are mostly coming from soil that is blown onto the lava surface, as well as aerosols being deposited. But later, after that winter shift in diversity they observed, they saw most of the microbes are coming from rainwater, and that's a pretty interesting result.
Scientists have long known that rainwater is not sterile; microbes in the atmosphere, either free floating or attached to dust particles, can even function as cloud condensation nuclei, which are microscopic particles that offer water vapor a surface to latch on to and grow into tiny droplets. In other words, tiny, invisible creatures may play outsized roles in weather and climate phenomena.
Nathan Hadland et al, Three eruptions at the Fagradalsfjall Volcano in Iceland show rapid and predictable microbial community establishment, Communications Biology (2025). DOI: 10.1038/s42003-025-09044-1
Can 'miracle' heaters really warm your home for pennies? The physics says no
Claims that portable electric heaters can heat homes for pennies or rapidly warm entire houses are not supported by physics. All electric heaters are nearly 100% efficient, meaning almost all input electricity becomes heat, but this does not make them cheap to run. No plug-in heater can outperform others in efficiency or safely deliver enough power to heat a whole house quickly. Heat pumps offer greater efficiency by moving heat rather than generating it, but are costly to install. Effective home heating relies on better insulation, efficient systems, and affordable energy, not miracle devices.
Urban birds' beak shape rapidly changed during COVID-19 lockdowns, suggesting human-driven transformations During the COVID-19 lockdowns, urban dark-eyed juncos developed longer, thinner beaks resembling their wild counterparts, likely due to reduced human food waste. As human activity resumed, beak shapes reverted to the shorter, thicker form typical of urban birds. These rapid, reversible changes highlight the strong influence of human presence on urban bird morphology.
When the world slowed down during the COVID-19 pandemic, its effects extended beyond humans. A recent study found that it reshaped urban ecosystems to such an extent that certain city-dwelling birds even began to develop longer, thinner beaks resembling those of their wild relatives.
The dark-eyed junco is a small, grayish songbird that is a common winter guest across North America.
A research duo from the University of California, Los Angeles, identified that the juncos living on campus were an ideal system for exploring how physical traits change in urban environments. They tracked changes in the birds across the pre-pandemic and post-pandemic periods, from 2018 to 2025.
They observed that birds that hatched during the pandemic, when the campuses became empty and there was less food waste to feed on, had beaks with higher bill length and slimmer structure, similar to the wildland birds. However, after the COVID-19 restrictions were lifted and people started trickling back to campus and food waste became ample. Birds born during this period reflected this shift, exhibiting shorter, thicker beaks typical of urban juncos.
Studies have shown that animals living in cities can undergo rapid phenotypic changes — observable alterations in an organism's traits or characteristics—in response to newer environments, necessary to increase their chances of survival and the urban setting.
The juncos living in California, U.S. are no longer winter visitors, they have become year-round residents over the past few decades. As a result, these birds appear to have adapted to urban life by evolving physical traits that help them thrive in city landscapes.
One of the most striking changes is in their beaks. Juncos living in Los Angeles have shorter, thicker beaks than those found in local mountainous forests. Scientists think that this change might be linked to their diet, which now includes human food waste rather than the seeds, worms, and insects that wild juncos typically eat.
The period of global slowdown caused by COVID-19 lockdowns, now known as the anthropause, gave scientists a rare chance to see how animals physically changed when human activity suddenly decreased.
the researchers found that the anthropause corresponded with changes in bill shape and size. Birds hatched during the pandemic had beaks similar to wild juncos, but as human activity picked up again, their beaks reverted to the short, stout form seen in urban populations. These results indicate that city birds quickly adjusted their behavior when human activity stopped and started again.
The researchers note that further genetic and behavioral studies in both urban and wildland populations are needed to confirm whether these shifts were driven by genetic changes triggered by low human activity or temporary movements of wild birds into the city during the pandemic.
Eleanor S. Diamant et al, Rapid morphological change in an urban bird due to COVID-19 restrictions, Proceedings of the National Academy of Sciences (2025). DOI: 10.1073/pnas.2520996122
Mitochondria migrate toward the cell membrane in response to high glucose levels, study shows In pancreatic beta cells, high glucose levels cause mitochondria to migrate toward the cell periphery. This movement depends on intact microtubules and cAMP signaling, but not on mitochondrial ATP production. Peripheral redistribution of mitochondria may influence insulin secretion, suggesting spatial organization of mitochondria is important for beta cell function.
Bacterium hijacks fruit ripening program in citrus plants to steal sugars, research reveals Xanthomonas citri, the causative agent of citrus canker, manipulates citrus leaf cells by activating a fruit ripening program, leading to the release of cell wall-bound sugars that fuel rapid bacterial growth. This process mimics natural fruit ripening at the genetic level and highlights a mechanism by which pathogens access otherwise inaccessible nutrients, offering potential strategies for developing disease-resistant citrus varieties.
Trang Thi-Thu Phan et al, Xanthomonas coordinates type III–type II effector synergy by activating fruit-ripening pathway, Science (2025). DOI: 10.1126/science.adz9239
Is aging an act of genetic sabotage? Scientists find a gene that turns off food detection after reproduction
A gene called nhr-76 in roundworms actively suppresses food-odor detection after reproduction by switching off related sensory genes in neurons. This programmed decline, rather than accumulated damage, suggests aging can involve active genetic regulation. Similar genes in mammals may play related roles, but their effects in humans remain unconfirmed.
Rikuou Yokosawa et al, A Nuclear Hormone Receptor nhr‐76 Induces Age‐Dependent Chemotaxis Decline in C. elegans, Aging Cell (2025). DOI: 10.1111/acel.70277
Global food systems driving twin crises of obesity and global warming, says review Unsustainable, profit-driven food systems promote high-calorie, low-fiber diets, contributing to rising obesity and significant greenhouse gas emissions. Animal-based and ultra-processed foods are key drivers of both health and environmental harms. System-level reforms—such as taxes, subsidies, and marketing restrictions—are recommended to improve diets and reduce climate impact.
A major review in Frontiers in Science highlights how tackling unsustainable food systems—reflected by our changing food environment—is urgent for both health and climate.
Thepaperreviews evidence that both obesity and environmental harms result from a profit-led food system that encourages high intake and poor health. The authors say that our food environment promotes high-calorie, low-fiber products such as some ultra-processed foods (UPFs)—the most caloric of which encourage weight gain.
Those same production systems, especially involving animals, release large amounts of greenhouse gases and put pressure on land and water.
The comprehensive review says that addressing the food environment can therefore deliver double benefits for health and climate.
The authors recommend using subsidies for healthy foods, taxes and warning labels for particularly unhealthy foods, and restrictions on aggressive marketing of high-calorie, low-fiber products, particularly in low-income communities and to children.
They also counter the perception that weight-loss drugs are a panacea for obesity, as they do not address the systemic drivers which also harm the climate.
Obesity and climate change: co-crises with common solutions, Frontiers in Science (2025). DOI: 10.3389/fsci.2025.1613595
Antifungal vaccine heads for clinical trials A vaccine designed to protect against infections with certain fungal pathogens is set to move into phase I clinical trials, backed by US$40 million in funding from the US National Institutes of Health. The vaccine, called VXV-01, uses two antigens to elicit an immune response to fungal pathogens such as Candida auris and Candida albicans, which can cause drug-resistant infections in hospitals.
A team of international scientists has, for the first time, created a full picture of how errors unfold over time inside a quantum computer—a breakthrough that could help make future quantum machines far more reliable.
The researchers found that the tiny errors that plague quantum computers don't just appear randomly. Instead, they can linger, evolve and even link together across different moments in time.
The team has made its experimental data and code openly available, and the full study is published in Quantum.
This type of behavior is one of the key obstacles to building practical, large-scale quantum computers.
The team ran a series of experiments on cutting-edge superconducting quantum processors—some in the lab at the University of Queensland and others accessed through IBM's cloud-based quantum computers.
Previous attempts to map the behaviour of quantum systems over time all hit the same roadblock: after measuring a quantum system mid-experiment, scientists couldn't freely set it up again for the next step, because the setting-up depends on whether the result of the measurement was 0 or 1.
The new method solves this by adding a clever twist, assuming that 50% of the time, the result was 1, and the remaining time, the result was 0. Then, the researchers used software to work backwards with the data, to figure out what state it was in.
What they found is that even today's best quantum machines show subtle but important time-linked noisepatterns—including noise that is quantum in nature and comes from nearby qubits on the same chip.
Understanding these patterns will help quantum scientists design better characterization and error-correction tools, a crucial step toward building dependable, fault-tolerant quantum computers.
Ancient viral DNA shapes early embryonic development
A new study reveals how ancient viral DNA once written off as "junk" plays a crucial role in the earliest moments of life. The research, published in Science Advances, begins to untangle the role of an ancient viral DNA element called MERVL in mouse embryonic development and provides new insights into a human muscle wasting disease.
Transposable elements are stretches of DNA that can move around the genome. Many of these DNA sequences originate from long ago, when viruses inserted their genetic material into our ancestors' genomes during infection. Today, these viral transposable elements make up around 8-10% of the mammalian genome.
Once disregarded as "junk" DNA, we now know that many transposable elements play an important role in influencing how genes are turned on and off, especially during early development. They have a variety of beneficial and harmful roles in the body, for example, some help regulate normal immune responses, while others can disrupt genes and contribute to diseases like cancer.
The latest work focuses on a viral transposable element called MERVL.
This element becomes highly active for a short window of time when a mouse embryo reaches the two-cell stage—the point at which a fertilized egg has divided into two cells and switches on its own genome for the first time. Cells in this state are considered "totipotent," meaning they can generate every cell type of the embryo and extraembryonic tissues like the placenta.
MERVL acts as a central switch to activate a large network of genes specific to the two-cell stage of development.
To work out the role of MERVL, the team used a gene manipulation technique called CRISPR activation to turn on MERVL elements in mouse embryonic stem cells, to mimic what happens in two-cell embryos.
In cells where only MERVLwas activated, the cells looked like they were only partially similar to cells of the two-cell stage, but they still had several characteristics of totipotency. The researchers described this in-between state as an "intermediate phenotype." They showed that activating MERVL alone is sufficient to create totipotent features in early embryonic development.
New 'cloaking device' concept shields electronics from disruptive magnetic fields
Unwanted magnetic fields can disrupt the operation of precision instruments, sensors, and electronic components, leading to signal distortion, data errors, or equipment malfunction. This is a growing concern in environments such as hospitals, power grids, aerospace systems, and scientific laboratories, where increasingly sensitive technologies require effective protection from magnetic interference.
Researchers have unveiled a concept for a device designed to magnetically "cloak" sensitive components, making them invisible to detection. A magnetic cloak is a device that hides or shields an object from external magnetic fields by manipulating how these flow around an object so that they behave as if the object isn't there.
In Science Advances, the team of engineers demonstrate for the first time that practical cloaks can be engineered using superconductors and soft ferromagnets in forms that can be manufactured.
Using computational and theoretical techniques such as advanced mathematical modeling and high-performance simulations based on real-world parameters, they have developed a new physics-informed design framework that allows magnetic cloaks to be created for objects of any shape. Until now, cloaks were mostly theoretical or restricted to simple shapes like cylinders.
This study demonstrates for the first time how to design magnetic cloaks for the irregular geometries we see in the real world. These cloaks also maintain their effectiveness across a broad range of field strengths and frequencies.
Magnetic cloaks could play a vital role in protecting sensitive electronics and sensors from magnetic interference, which is a growing challenge in everything from medical devices to renewable energy and space technology.
Biophysicists uncover new electrical transmission in cells
Many biological processes are regulated by electricity—from nerve impulses to heartbeats to the movement of molecules in and out of cells.
A new study by search scientists reveals a previously unknown potential regulator of this bioelectricity: droplet-like structures called condensates. Condensates are better known for their role in compartmentalizing the cell, but this study shows they can also act as tiny biological batteries that charge the cell membrane from within.
The team showed that when electrically charged condensates collide with cell membranes, they change the cell membrane's voltage—which influences the amount of electrical charge flowing across the membrane—at the point of contact.
The discovery, published in the journalSmall, highlights a new fundamental feature about how our cells work, and could one day help scientists treat certain diseases.
Condensates are organelles—structures within cells that carry out specific functions—but unlike more well-known organelles such as the nucleus and mitochondria, they are not enclosed within membranes. Instead, condensates are held together by a combination of molecular and electrical forces. They also occur outside of cells, such as at neuronal synapses.
Condensates are involved in many essential biological processes, including compartmentalizing cells, protein assembly and signaling both within and between cells. Previous studies have also shown that condensates carry electrical charges on their surfaces, but little is known about how their electrical properties relate to cellular functions.
If condensates can alter the electrical properties of cell membranes, it could have big implications, because many cellular processes are controlled by changes in the cell membrane voltage. For example, ion channels—proteins that rapidly transport molecules across the cell membrane—are activated by changes in cell membrane voltage. In the nervous system, this rapid, one-directional transport of electrically charged molecules is what drives the propagation of electrical signals between nerves.
To test whether condensates can alter cell membrane voltage, the researchers used cell models called Giant Unilamellar Vesicles (GUVs). To allow them to visualize changes in voltage, they stained GUV membranes with a dye that changes color in response to changes in electrical charge. Then, they put GUVs in the same vessel as lab-made condensates and photographed their interactions under the microscope.
They showed that when the condensates and GUVs collided, it caused a local change in the GUV membranes' electrical charge at their point of contact. By varying the chemical makeup of the condensates, the researchers showed that the more electrical charge a condensate carried, the bigger its impact on cell membrane voltage. They also found that the shape of the condensates appeared to be correlated with variations in the voltage change.
In some instances, the voltages induced are quite substantial in magnitude—on the same scale as voltage changes in nerve impulses.
Anthony Gurunian et al, Biomolecular Condensates Can Induce Local Membrane Potentials, Small (2025). DOI: 10.1002/smll.202509591
Earth's Seasons Are Strangely Out of Sync, Scientists Discover From Space
Scientists have watched our planet's seasons from space and discovered that spring, summer, winter, and fall are surprisingly out of sync.
Just because two places exist in the same hemisphere, at similar altitudes, or at the same latitude doesn't guarantee they'll experience the same seasonal changes at the same time.
Even regions that are side by side can experience different weather and ecological patterns, sculpting wildly different neighboring habitats.
It's similar to how time zones can separate two adjacent spots, but in this case, the boundary is drawn by nature itself.
Using 20 years of satellite data, researchers have created what they say is the most comprehensive map to date of the seasonal timing of Earth's terrestrial ecosystems.
The new map identifies global regions where seasonal patterns are particularly out of sync, and these asynchronies often occur in biodiversity hotspots. That is probably no coincidence. More variability in weather patterns can have trickle-down effects, which may drive greater diversity within habitats. For example, if natural resources in two neighboring habitats are made available at different times of the year, it could shape the ecology and evolution of flora and fauna in each spot.
It could even mean that a species in one habitat reaches its reproductive season before or after the same species in an adjacent habitat, preventing interbreeding. Across many generations, this can lead to the evolution of two entirely separate species.
Most People Develop Diverticulosis in Their Gut by Age 80
It's easy to see your body aging on the outside – wrinkles, dark spots, gray hair, the whole shebang – but as we grow older, our insides also inevitably change.
By the time most people reach the ripe age of 80, the smooth lining of their digestive tract is scattered with small, bulging pouches of tissue.
These sac-like protrusions along the digestive tract, called diverticula, are 'weak spots' in the gut's muscular wall. They are typically harmless, and most people never even know they are there.
Sometimes, after a colonoscopy, patients are alarmed to find they have developed diverticulosis, but most of the time, this condition is nothing to worry about.
Only if the pouches become inflamed or infected is it considered diverticular disease, or diverticulitis. Symptoms, which generally come and go, often include constipation, diarrhea, abdominal pain, bloating, or fever.
The good news is that even if a person does develop diverticulitis, their symptoms usually improve with just a few days of bed rest and a liquid diet. Over 85 percent of patients find this sufficient.
No one knows exactly what causes diverticula to form in the first place, but current treatments generally focus on helping the digestive tract move smoothly, without blockages.
That's why a high-fiber diet, including between 25 and 30 grams of fiber a day, is often recommended to recovering patients. This won't heal existing diverticula, but may prevent more from forming.
Other potential risk factors include obesity, lack of exercise, and smoking. There's likely a complicated mix of contributing factors.
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While diverticula can develop in the large and small intestine, around 95 percent of patients in the Western world have diverticula in their sigmoid colon.
This part of the digestive tract works under great pressure to push feces into the rectum.
Once diverticula form, possibly from excessive pressure, they are prone to bleeding when aggravated, in a similar way to hemorrhoids, which form inside and outside the rectum and around the anus. Diverticular bleeding is estimated to cause between 30 and 65 percent of all cases of lower gastrointestinal bleeding. It's usually painless and self-limiting, but seeing blood in the stool is a serious matter, as it may indicate other severe conditions. Treatment depends on the severity of the episode.
2.8 days to disaster: Why we are running out of time in low earth orbit
Satellite mega-constellations in low Earth orbit experience close approaches every 22 seconds, with each satellite performing frequent avoidance maneuvers. Solar storms increase atmospheric drag and can disable satellite control systems, raising collision risks. If operators lose control, a catastrophic collision could occur within 2.8 days, compared to 121 days in 2018, highlighting increased vulnerability.
Sarah Thiele et al, An Orbital House of Cards: Frequent Megaconstellation Close Conjunctions, arXiv (2025). DOI: 10.48550/arxiv.2512.09643
Physicists crack a 'Big Bang Theory' problem that could help explain dark matter Theoretical work demonstrates that axions, hypothetical particles considered a candidate for dark matter, could be produced in fusion reactors using deuterium, tritium, and lithium. Neutron interactions with reactor walls and bremsstrahlung processes may generate axions or axion-like particles, offering a new approach to probing dark matter beyond solar-based searches.
Chaja Baruch et al, Searching for exotic scalars at fusion reactors, Journal of High Energy Physics (2025). DOI: 10.1007/jhep10(2025)215
The moon-forming event: Why it was by explosive ejection rather than a giant impact A new model proposes that the Moon formed from explosive ejection of Earth's mantle and crust, driven by accumulated internal gravitational energy (LɅ) released at the core-mantle boundary, rather than by a giant impact. This mechanism explains the Moon's isotopic similarity to Earth and links geophysical processes, such as mantle plumes and LLVPs, to lunar formation.
Matthew R. Edwards, Explosive lunar fission above a large low-velocity province, Acta Geochimica (2025). DOI: 10.1007/s11631-025-00834-2
Scientists observe 'extraordinary' seven-arm octopus A rare deep-sea encounter captured footage of the seven-arm octopus, Haliphron atlanticus, at 700 meters depth in Monterey Bay. This species, with females reaching up to 4 m and 75 kg, primarily inhabits the ocean's twilight zone and feeds on gelatinous animals such as jellyfish, supporting previous observations of its unusual diet.
Hoving, H.J.T. and S.H.D. Haddock. 2017. The giant deep-sea octopus Haliphron atlanticus forages on gelatinous fauna. Scientific Reports, 7: 44952.https://doi.org/10.1038/srep44952
Natural daylight can help people with diabetes improve blood sugar levels
People with type 2 diabetes may be able to improve their blood sugar by doing something as simple as sitting by a window for a few hours each day. In a study published in Cell Metabolism, scientists showed that natural daylight helps maintain healthy glucose levels.
Daylight is known to be a mood enhancer and also beneficial for our health. However, according to the research team, most people living in Western societies typically stay indoors around 80% to 90% of the time under artificial light, which is not as bright or dynamic as sunlight. This is important because the human body operates on circadian rhythms, internal 24-hour clocks that orchestrate a range of biological processes, such as digestion and temperature regulation. These are synchronized by light, and a lack of natural light is a risk factor for type 2 diabetes.
Previous studies have shown that artificial light at night disrupts these rhythms and that daylight outdoors can improve the body's response to insulin, which helps control blood sugar levels. But no prior research examined how natural light entering a window affects people with diabetes.
To test this, researchers recruited 13 volunteers with type 2 diabetes to examine how their bodies responded to both natural window lighting and artificial indoor lighting. The participants spent two separate 4.5-day periods in a controlled office environment. In one session, they sat at a desk facing large windows from morning to late afternoon. In the other, they were in the same room, with the windows blocked and only standard office lights. All participants ate similar meals three times a day and performed the same exercises at the same time across the two sessions. They also continued taking their medication.
The results revealed that while average glucose levels were similar across the two sessions, the participants spent significantly more time in the normal glucose range when exposed to natural daylight. The body's metabolism also changed. In daylight, the volunteers burned more fat for energy and fewer carbohydrates.
The researchers also took muscle biopsies and grew muscle cells in the lab. They found that genes involved in their internal cellular clocks were better aligned to the time of day under natural light. This suggested that sunlight was acting as a signal to keep the muscles "on time," making them better at processing nutrients.
Although this study involved only a handful of people, the results indicate that natural daylight can help reduce the sharp peaks and swings in blood sugar that often affect those with this condition. It offers a simple, natural way to support people with type 2 diabetes alongside existing treatments.
Jan-Frieder Harmsen et al, Natural daylight during office hours improves glucose control and whole-body substrate metabolism, Cell Metabolism (2025). DOI: 10.1016/j.cmet.2025.11.006
Scientists who use AI tools are publishing more papers than ever before
Science is entering a massive publishing boom, in large part due to artificial intelligence. New research published in the journal Science has revealed that scientists who use large language models (LLMs) like ChatGPT are producing significantly more papers across many fields. The technology is also helping to level the playing field for researchers whose first language isn't English.
The growing use of AI in scientific research has sparked concerns about shoddy work and machines making things up. But this new analysis also reveals that papers produced with LLMs use more complex language and cite a wider array of sources.
They found that when scientists use AI, their productivity soared. The biggest jump was in the social sciences and humanities, where output increased by 59.8%, while biology and life sciences saw a 52.9% increase. Meanwhile, in physics and math, the scientists report a 36.2% boost. "LLM adoption is associated with a large increase in researchers' scientific output," wrote the research team in their paper.
One of the most fascinating findings was the massive increase in productivity from non-English-speaking countries. Most top journals require manuscripts to be written in high-level English, which has long disadvantaged these scientists. But with AI handling some of the workload, researchers from Asia saw their output jump by as much as 89% in some cases. However, the study authors also issued a warning regarding AI and quality. While the machines can make papers sound more professional, this can be a trap. Historically, sophisticated writing was a sign of high-quality research, but now the opposite can sometimes be true. The study found that the more complex the AI-generated writing was, the less likely the paper was to be high quality. In other words, good writing can mask weak ideas.
The clear message from the study authors is that we can no longer judge a paper by how smart the language appears. "As traditional heuristics break down, editors and reviewers may increasingly rely on status markers such as author pedigree and institutional affiliation as signals of quality, ironically counteracting the democratizing effects of LLMs on scientific production."
To safeguard scientific integrity, the researchers propose several measures, including that institutions implement deeper checks and even specialized "AI-based reviewer agents" to help distinguish between human writing and machine-generated writing.
Keigo Kusumegi et al, Scientific production in the era of large language models, Science (2025). DOI: 10.1126/science.adw3000
How chirality goes from the molecular level to the cellular one
Researchers have discovered how right-handed molecules in our cells can give rise to cells that are not symmetrical about their central axes. This discovery is a key step toward determining why most of our organs lack left–right symmetry.
It's conceivable that if some molecules that make up our cells were twisted in the opposite direction, our hearts would be on the right side of our bodies rather than on the left.
That's because the difference between the left and right sides of our organs may originate from the "handedness," or chirality, of cells, which in turn comes from the chirality of molecules in cells.
However, the link between the chirality of molecules and cellular chirality is largely unknown. Many molecules in cells are chiral, including DNA and some amino acids and proteins, but it's not clear which ones convey their chirality to cells.
By studying the chiral behaviours of individual cells, researchers have found that the cells' scaffolding, or cytoskeleton, gives rise to the cell's chirality. The findings are published in the journal eLife.
When single cells were placed on a substrate, their nuclei and surrounding cytoplasm rotated in a clockwise direction when viewed from above. This rotational motion is driven by the concentric pattern of the actomyosin filaments that make up the cytoskeleton.
This finding implies that the cell nucleus can rotate even when there is no chiral orientation of the cytoskeleton on a cellular level. To confirm whether this mechanism was driving the rotation, the team created a 3D theoretical model of a cell and evaluated the effect of the molecular chirality of actin and myosin on it. The results revealed that the molecular scale torque generated by individual components of the cytoskeleton can generate rotation, even when cell-level chiral structures were absent.
These results help fill in a critical link in the chain from molecules to organs and bodies, the researchers say.
Takaki Yamamoto et al, Epithelial cell chirality emerges through the dynamic concentric pattern of actomyosin cytoskeleton, eLife (2025). DOI: 10.7554/elife.102296
PFAS concentrations can double with every step up the food chain PFAS concentrations increase twofold on average with each step up the food chain, resulting in significantly higher levels in top predators and humans. Analysis of 119 global food webs shows substantial variation among PFAS compounds, with some newer alternatives magnifying even more than legacy chemicals. These findings highlight the need for compound-specific regulation and further research into health impacts.
The authors examined 119 aquatic and terrestrial food webs across the globe, finding that top predators such as large fish, seabirds, and marine mammals can accumulate PFAS concentrations exponentially larger than the environments in which they're found. The study is published in the journal Nature Communications.
PFAS concentrations double, on average, with each step up the food chain.
Known as "forever chemicals," PFAS are from a family of more than 12,000 man-made compounds. These chemicals are prized for their heat resistance and water-repelling properties, and are used in cleaning products, food packaging, non-stick pans, clothing, and fire-fighting equipment.
Since being discovered by the American chemical company DuPont in the 1930s, PFAS are now detectable in the bloodstream of almost every human being on the planet.
Unlike other chemicals, PFAS never break down, meaning that throughout the world right now, they're building up in environments, plants, and animals on land and in the ocean.
For humans, sitting as we do at the top of the food chain, this means our diets can be an important pathway for PFAS exposure.
Given what we know about PFAS toxicity from other studies, these extreme accumulation rates in top predators suggest serious health risks. This creates a cascading ecological risk: Apex predators face disproportionately high exposure even in relatively low-contaminated environments.
Some compounds—including chemicals marketed as safer alternatives to existing products—showed even higher magnification than the chemicals they were designed to replace.
Lorenzo Ricolfi et al, Unravelling the magnitude and drivers of PFAS trophic magnification: a meta-analysis, Nature Communications (2025). DOI: 10.1038/s41467-025-65746-4
More eyes on the skies can help planes reduce climate-warming contrails
Aviation's climate impact is partly due to contrails—condensation that a plane streaks across the sky when it flies through icy and humid layers of the atmosphere. Contrails trap heat that radiates from the planet's surface, and while the magnitude of this impact is uncertain, several studies suggest contrails may be responsible for about half of aviation's climate impact. Geostationary satellites detect only about 20% of contrails visible to low-Earth-orbiting satellites, primarily missing smaller, younger contrails. Combining data from geostationary, low-Earth-orbit, and ground-based observations can provide a more complete understanding of contrail formation and evolution, supporting more effective contrail avoidance strategies to mitigate aviation's climate impact.
Pilots could conceivably reduce their planes' climate impact by avoiding contrail-prone regions, similarly to making altitude adjustments to avoid turbulence. But to do so requires knowing where in the sky contrails are likely to form.
To make these predictions, scientists are studying images of contrails that have formed in the past. Images taken by geostationary satellites are one of the main tools scientists use to develop contrail identification and avoidance systems.
But a new study shows there are limits to what geostationary satellites can see.
Researchers analyzed contrail images taken with geostationary satellites, and compared them with images of the same areas taken by low-Earth-orbiting (LEO) satellites. LEO satellites orbit Earth at lower altitudes and therefore can capture more detail. However, since LEO satellites only snap an image as they fly by, they capture images of the same area far less frequently than geostationary (GEO) satellites, which continuously image the same region of Earth every few minutes.
The researchers found that geostationary satellites miss about 80% of the contrails that appear in LEO imagery. Geostationary satellites mainly see larger contrails that have had time to grow and spread across the atmosphere. The many more contrails that LEO satellites can pick up are often shorter and thinner. These finer threads likely formed immediately from a plane's engines and are still too small or otherwise not distinct enough for geostationary satellites to discern. The study highlights the need for a multiobservational approach in developing contrail identification and avoidance systems. The researchers emphasize that both GEO and LEO satellite images have their strengths and limitations.
Observations from both sources, as well as images taken from the ground, could provide a more complete picture of contrails and how they evolve.
With more 'eyes' on the sky, we could start to see what a contrail's life looks like, the researchers conclude.
Marlene V. Euchenhofer et al, Contrail Observation Limitations Using Geostationary Satellites, Geophysical Research Letters (2025). DOI: 10.1029/2025gl118386
Biodegradable electronics can break down into harmful microplastics Some materials used in biodegradable electronics, such as PEDOT:PSS, can persist for years and degrade into microplastics, raising environmental concerns. In contrast, polymers like cellulose and silk fibroin degrade more safely. The environmental impact of both material choice and manufacturing processes is significant, highlighting the need for sustainable, circular approaches in electronics production.
Sofia Sandhu et al, End-of-Life usefulness of degradation by products from transient electronics, npj Flexible Electronics (2025). DOI: 10.1038/s41528-025-00411-w
People are getting their news from AI—and it's altering their views
Large language models increasingly shape public opinion by generating news content and summaries, often introducing subtle communication bias by emphasizing certain viewpoints while minimizing others, even when information is accurate. This bias stems from model design, training data, and market concentration. Current regulations focus on harmful outputs but are less effective against nuanced framing biases, highlighting the need for greater competition, transparency, and user involvement.
Scientists chart over 140,000 DNA loops to map human chromosomes in the nucleus Over 140,000 DNA looping interactions were mapped in human embryonic stem cells and fibroblasts, providing a detailed 3D organization of chromosomes within the nucleus. Computational models now predict genome folding from DNA sequence alone, clarifying how chromatin loops influence gene regulation and how genetic variations may alter genome structure and function.
Job Dekker et al, An integrated view of the structure and function of the human 4D nucleome,Nature(2025).DOI: 10.1038/s41586-025-09890-3
Two ancient human species came out of Africa together, not one, suggests new study
The textbook version of the "Out of Africa" hypothesis holds that the first human species to leave the continent around 1.8 million years ago was Homo erectus. But in recent years, a debate has emerged suggesting it wasn't a single species, but several. New research published in the journal PLOS One now hopes to settle the matter once and for all.
The debate centers on the Dmanisi fossils, five skulls found in the Republic of Georgia between 1999 and 2005, which belong to some of the oldest humans ever found outside Africa. The problem is that they don't look alike. Some are larger than others, particularly Skull 5, which has a tiny braincase but a massive, protruding face. Some researchers explain this as a difference in sexes within the same species, while others argue that it represents two distinct species living together.
To provide much-needed clarity, researchers studied the teeth of three Dmanisi specimens. The reason is that, generally, skulls are not always the best species identifiers because bone is fragile and can be warped and crushed. Dentition is far more useful because enamel is the hardest biological substance produced by humans, and everything from the shape and size of individual teeth can be used to identify a species.
The team focused on the surface area (dental crown) of the back teeth (premolars and molars) of the Dmanisi specimens that had sufficient dental remains for analysis. They compared these to a database of 122 other fossil specimens, including Australopithecus and several other Homo species. Then, using a statistical sorting tool, they analyzed 583 teeth to create a biological map and determine whether the Dmanisi fossils belonged to a single family or to other branches of our family tree.
The map revealed that these ancient remains were not from a single group. Skull 5, with its large jaw, was grouped with Australopiths, a more primitive ape-like ancestor. The other two specimens were more human-like. Because of this, the study authors support using the names Homo georgicus for Skull 5 and Homo caucasi for the human-like group.
To ensure the differences weren't just between males and females, the team compared the fossils with those of great apes. In some animals, like gorillas, males are much larger than females but still have the same basic teeth. The differences between the Dmanisi teeth were so great that male-female differences within the same group couldn't explain them.
Part 1
The postcanine dental crown area analysis of the Dmanisi hominin fossils... supports the hypothesis of distinct species coexisting temporally at the site (Homo caucasi and Homo georgicus). This possibility challenges the prevailing model of Homo erectus migration out of Africa..." commented the researchers in their paper.
While the research lends weight to the idea that two species left Africa at roughly the same time, more specimens may be needed before a consensus is reached.
Victor Nery et al, Testing the taxonomy of Dmanisi hominin fossils through dental crown area, PLOS One (2025). DOI: 10.1371/journal.pone.0336484
Some mammals can hit pause on a pregnancy—understanding how that happens could help us treat cancer Embryonic diapause allows some mammals to pause development by activating a molecular brake that suppresses differentiation pathways, maintaining stem cell pluripotency during metabolic stress. This mechanism involves the displacement of Capicua, enabling genes that inhibit the MAP kinase pathway. The findings suggest similar dormancy programs may underlie long-term survival in immune, stem, and cancer cells.
Tuo Zhang et al, Transcriptional derepression of negative regulators of MAP kinase supports maintenance of diapause ES cells in the pluripotent state, Genes & Development (2025). DOI: 10.1101/gad.353143.125
Whale, dolphin strandings show widespread disease, trauma Analysis of 272 cetacean strandings in the Pacific Islands from 2006 to 2024 found that over 65% involved disease or human-caused trauma. Disease accounted for 62% of cases, with infectious agents like morbillivirus and brucella affecting multiple species. Human-related trauma, including vessel strikes and debris ingestion, contributed to 29% of strandings.
From land-borne pathogens to high-speed vessel strikes, Pacific whales and dolphins are caught in a "perfect storm" where human-caused trauma and infectious diseases were found in more than 65% of investigated strandings.
A study spanning nearly two decades by researchers provides insights into the threats whales and dolphins face in the Pacific Islands.
Based on 272 stranding investigations of 20 cetacean species between 2006 and 2024, the study provides foundational data to better manage and conserve Hawaiʻi's whales and dolphins. The findings are published in the journal Diseases of Aquatic Organisms.
Over 18 years, scientists examined more than three-quarters of the stranded whales and dolphins to understand why they died. Most cases (62%) were linked to diseases, and about half of those animals were in poor body condition due to long-term illness. Infectious agents proved to be a significant threat, affecting 11 different species, including striped dolphins and Longman's beaked whales. Two of the most concerning pathogens were morbillivirus and brucella, which can cause serious brain and lung problems in marine mammals.
Toxoplasmosis—a parasite that infects warm-blooded animals and spreads through cat feces across the environment—was responsible for the deaths of two spinner dolphins and one bottlenose dolphin.
The study revealed that 29% of all strandings were linked to anthropogenic (human-caused) trauma. Vessel strikeswere a significant risk, resulting in fatal vertebral and skull fractures for seven individuals, including two pygmy sperm whales, two humpback whale calves, a goose-beaked whale, a spinner dolphin and a striped dolphin.
Interactions with marine debris and fisheries were confirmed as fatal in multiple cases, including a sperm whale that died from plastic and fishery debris blocking its stomach and a bottlenose dolphin that died after a fishhook tore into it.
Kristi West et al, Pacific Islands cetaceans: a review of strandings from 2006-2024, Diseases of Aquatic Organisms (2025). DOI: 10.3354/dao03877
Gut bacteria may play role in bipolar depression by directly influencing brain connectivity
Bipolar disorder (BD) is a psychiatric disorder characterized by extreme mood changes. Individuals diagnosed with BD typically alternate between periods of high energy, euphoria, irritability and/or impulsivity (i.e., manic episodes) and others marked by feelings of sadness, low energy, and hopelessness (i.e., depression).
While there are now several medications that can help patients to manage the disorder and stabilize their mood, many of these drugs have side effects and dosages often need to be periodically adjusted. Recent studies suggest that the bacteria and microorganisms living in the digestive system, also known as gut microbiota, play a key role in mental health and might also contribute to some symptoms of BD.
Researchers recently carried out a study investigating the possible connection between gut microbiota and the depressive episodes experienced by people diagnosed with BD. Their findings, published in Molecular Psychiatry, suggest that the microorganisms in the digestive system can directly influence connections between specific brain regions known to be affected by BD depression.
Adequate evidence has shown that gut microbial dysbiosis is an emerging disease phenotype of BD and is closely related to clinical symptoms of this intractable disease, wrote the researchers in their paper.
To explore the link between gut microbiota and BD depression, the researchers collected gut bacteria from individuals diagnosed with BD who were going through a depressive phase. They then transplanted these bacteria into the digestive system of healthy mice.
They found that bipolar depression-like mice presented with a decrease in the density of dendrite spines in medial prefrontal neurons, and translation post-synapse as a key contributor to the changes in synaptic plasticity.
In addition, analysis of synaptic connectivity in the mPFC revealed that compared to control mice, fewer connections were observed between ventral tegmental area and mPFC glutamate neurons and dopamine response was decreased in BD mice.
Notably, the researchers found that after they received the microbiota taken from individuals who were experiencing BD depression, the mice also started exhibiting depression-like behaviors. In addition, neurons in two brain regions known to be implicated in mood regulation, namely the ventral tegmental area (VTA) and the medial prefrontal cortex (mPFC), appeared to be less connected with each other.
The team also observed disruptions in the production of proteins and reduced dopamine signaling. Dopamine signaling (i.e., the release of dopamine) is essential for maintaining motivation and emotional regulation.
The results of this study confirm that microorganisms and bacteria in the gut can influence the connections between neurons in different brain regions. These altered connections could in turn have an impact on motivation, mood regulation and the processing of emotions.
The team's findings will need to be validated in humans before they can be reliably translated into psychiatric and medical insight. In the future, however, they could potentially help to identify promising pathways for the treatment of depression in patients diagnosed with BD, which are designed to alter their gut microbiota.
Anying Tang et al, Gut microbiota modulates synaptic plasticity, connectivity, and dopamine transmission in the VTA-mPFC pathway in bipolar depression, Molecular Psychiatry (2025). DOI: 10.1038/s41380-025-03398-y.
Brain chemistry can reactivate or suppress dormant HIV
Human immunodeficiency virus (HIV) infections are still fairly common and an estimated 40 million people worldwide are currently living with this condition. The HIV virus attacks the body's immune system and thus makes those who contract it more vulnerable to a wide range of infections.
While there is still no known cure for HIV, there are now various treatment options that allow affected patients to live long and healthy lives. When treated with antiretroviral therapy (ART), the virus is known to remain in a latent state, essentially 'hiding' inside cells and forming a reservoir of dormant virus. If the medication is stopped, however, the virus can be re-awoken, causing severe immune deficiencies again.
Researchers have recently been investigating how the brain, particularly tiny molecules and protein-carrying packages released by cells, influence the persistence of HIV. In a new paper, published in Molecular Psychiatry, they presented new findings that shed new light on molecular mechanisms that can either re-ignite or suppress latent HIV.
In their experiments the researchers found that ECs collected from the brains of SIV-infected but untreated macaques strongly re-activated latent virus reservoirs increasing the activity of viral genes, the production of proteins and causing the virus to spread between cells. Interestingly, however, particles extracted from the brains of infected macaques who were treated with cannabinoids were found to suppress the re-activation of the virus.
"Cannabinoids have been shown to inhibit neuroinflammation," said the authors of the research paper. They showed that cannabinoids exert similar anti-inflammatory effects via EVs and in the current study on ECs, we report that ECs isolated from brains (basal ganglia) of rhesus monkeys have this anti-inflammatory effect and that cannabinoids modulate the cargos of the ECs, with resultant effects on latent HIV reservoirs.
Overall, the findings gathered by these researchers suggest that the brain's chemistry, particularly ECs, do play a key role in the reactivation or suppression of dormant HIV. In the future, their work could pave the way for the development of new drugs and therapeutic interventions aimed at better managing, or perhaps even curing, HIV infections.
Wasifa Naushad et al, Extracellular condensates (ECs) are endogenous modulators of HIV transcription and latency reactivation, Molecular Psychiatry (2025). DOI: 10.1038/s41380-025-03354-w.
The global fish trade is spreading 'forever chemicals' around the world
Eating fish may well be good for you, but it carries a hidden risk of exposure to so-called "forever chemicals." A new study published in the journal Science has revealed that the global seafood trade is acting as a massive delivery system for per- and polyfluoroalkyl substances (PFAS), industrial pollutants that persist in the environment for decades.
These forever chemicals are used in many products, from nonstick cookware and cosmetics to food packaging and firefighting foams. They are extremely resistant to breaking down in the environment and have been linked to a variety of serious illnesses such as cancer and liver disease.
PFAS can travel long distances around the planet in the air and through water. Once they wash into the ocean, they are absorbed by tiny organisms at the bottom of the food chain, such as plankton and algae. Because these chemicals do not break down, they accumulate in their bodies, and when small fish eat them, the toxic substances pass up the food chain. Large predatory fish, the kind that end up on our dinner plates, eat these smaller marine creatures, and as a result, the chemical concentrations build up in their tissues and organs.
In their paper, the researchers set out to map how these chemicals move once they are inside the fish. They built a computer model covering 212 different species to track how toxins accumulate up the food chain and then validated this with lab tests on fish from numerous countries. Then the team combined this data with global trade records to see how the fish and PFAS travel from one country to another.
One of the most significant findings was that the international fish trade acts like a global conveyor belt, redistributing PFAS from contaminated regions to consumers thousands of miles away. Before this study, it was generally assumed that forever chemicals were a local problem. If your country's rivers and seas were clean, then so were the fish. However, a nation with clean water can still be exposed to high levels of PFAS through the seafood it imports from other parts of the world. For example, researchers found that Italians buy only 11% of their fish from Sweden, yet this accounts for more than 35% of their PFAS exposure.
Given that this problem doesn't respect borders, researchers argue that a unified global strategy is needed to protect public health.
Wenhui Qiu et al, Risks of per- and polyfluoroalkyl substance exposure through marine fish consumption,Science(2025).DOI: 10.1126/science.adr0351
Jennifer Sun et al, Reevaluating PFAS exposure risks from marine fish,Science(2025).DOI: 10.1126/science.aed7431
Raindrops form 'sandballs' as they roll downhill, contributing more to erosion than previously thought
We know that the initial splash of raindrops on soil contributes to erosion, but a new study, published in the Proceedings of the National Academy of Sciences, finds that the journey of the raindrop downhill might have an even bigger impact on erosion than the initial splash.
Researchers observed natural raindrops hitting the surface of a hillside and noticed that they collected particles of sand as they rolled downhill. This spurred the researchers to document the event with a camera and then take the idea to the lab.
In the lab, they constructed a 1.2 meter long bed covered with dry silicate sand and tilted at an angle of 30°. The lab conditions enabled the team to properly document the phenomenon by recording the evolution of the raindrops' shapes as they rolled and take precise measurements of the relevant parameters. They found that each raindrop formed what they refer to as "sandballs" and that they took on differing shapes, depending on the conditions, and that the sandballs can move up to 10 times more soil than the initial splash alone.
"In the initial rolling stage, drops rapidly increase their speed and sediment entrainment rate. Under increasing centrifugal force, the rolling drops undergo a metamorphosis: Their rounded shape destabilizes, as both liquid and entrained grains drift away from the core to create sandballs," the study authors write in their paper.
The researchers found that the sandy raindrops formed two distinct shapes: a peanut shape and a doughnut shape. Peanuts occurred at comparably lower velocities and maintained their grains at the surface of the drop. They only gather grains up to a certain point and then usually plateau.
"Once their mass plateaus, peanuts continue to increase their angular velocity as they roll; this sometimes causes a shift in their mode of motion, triggering an additional phase of mass accumulation. Other times, peanuts break, tumble slower or settle. If peanuts survive to the end of the slope and roll onto a flat surface, they immediately fall apart," the study authors explain.
Instead of only gathering grains at the surface, doughnut-shaped drops absorb sand grains into their interior volume, making them more dense and opaque in appearance. The researchers call the emergence of these kinds of drops "unexpected."
The team found that these drops destabilize into the doughnut shape from axisymmetric radial stretching. These shapes only occur at very high spin rates in pure-liquid drops, but occurred at slightly lower rates in the lab experiments due to the water-glycerol mixture used in the lab-based drops.
The study authors write, "Fully developed doughnuts continue to speed up (above 1 m/s), until a point where they sometimes break apart in an apparent fracture process. This breakage occurs when the tensile force driven by the centrifugal sandball stretching overcomes the strength of capillary bonds, producing child sandballs that carve their own track as they tumble down the slope."
Studying the shapes that raindrops take on as they tumble down dry dirt hills might seem frivolous, but these dynamics have real implications for soil erosion models, which are used for predicting soil loss from rain. These models help with conservation planning, land management, and environmental assessment by estimating erosion rates, identifying more vulnerable areas, designing control measures and evaluating land health in agriculture.
Bertil Trottet et al, Sandball genesis from raindrops, Proceedings of the National Academy of Sciences (2025). DOI: 10.1073/pnas.2519392122
New species are being discovered faster than ever before, study suggests
According to a new study published in Science Advances, scientists are discovering species quicker than ever before, with more than 16,000 new species discovered each year. The trend shows no sign of slowing, and the team behind the new paper predicts that the biodiversity among certain groups, such as plants, fungi, arachnids, fishes and amphibians is richer than scientists originally thought.
Researchers analyzed the taxonomic histories of roughly 2 million species, spanning all groups of living organisms. Between 2015 and 2020—the most recent period with comprehensive data—researchers documented an average of more than 16,000 new species each year, including more than 10,000 animals (dominated by arthropods and insects), 2,500 plants and 2,000 fungi.
and the good news is that this rate of new species discovery far outpaces the rate of species extinctions, which researchers calculated to about 10 per year.
These thousands of newly found species each year are not just microscopic organisms, but include insects, plants, fungi and even hundreds of new vertebrates.
The team also analyzed the rates of new species appearing over time to project how many species will be discovered and described in the future. For example, they projected that there might be as many as 115,000 fish species and 41,000 amphibian species, even though there are only about 42,000 fish and 9,000 amphibian species described now. They also projected that the final number of plant species might be over a half million.
Discovering new species is important because these species can't be protected until they're scientifically described.
Additionally, the discovery of new species contributes to finding new natural products for human benefit.
Spider and snake venoms and many plants and fungi also contain natural products with potential medicinal applications, including treatments for pain and cancer.
Beyond medicine, many species have adaptations that can inspire human inventions, such as materials mimicking the "super-clinging" feet that allow geckos to climb up vertical surfaces. Scientists are still just scratching the surface of what these species can do for humanity.
Xin Li et al, The past and future of known biodiversity: Rates, patterns, and projections of new species over time, Science Advances (2025). DOI: 10.1126/sciadv.adz3071
Fathers' microplastics exposure tied to their children's metabolic problems
Paternal exposure to microplastics in mice leads to metabolic dysfunction in offspring, with female progeny showing increased susceptibility to diabetes and altered gene expression linked to inflammation. These effects are associated with changes in sperm small noncoding RNAs, indicating a mechanism for transgenerational impact of environmental pollutants.
A new study has shown for the first time that a father's exposure to microplastics (MPs) can trigger metabolic dysfunctions in his offspring. The research, conducted using mouse models, highlights a previously unknown pathway through which environmental pollutants impact the health of future generations.
While MPs have already been detected in human reproductive systems, the study, published in the Journal of the Endocrine Society, is the first to bridge the gap between paternal exposure to MPs and the long-term health of the next generation (the "F1 offspring").
MPs are tiny plastic particles (less than 5 millimeters) resulting from the breakdown of consumer products and industrial waste. Metabolic disorders refer to a cluster of conditions—including increased blood pressure, high blood sugar, and excess body fat—that increase the risk of heart disease and diabetes.
Key findings and sex-specific effects The research team found that female offspring of male mice exposed to MPs were significantly more susceptible to metabolic disorders than offspring of unexposed fathers, despite all offspring being fed the same high-fat diet.
"The exact reasons for this sex-specific effect are still unclear", say the researchers. They observed upregulation of pro-inflammatory and pro-diabetic genes in their livers—genes previously linked to diabetes. These changes were not seen in male offspring. The research team found that while male offspring did not develop diabetes, they showed a slight yet significant decrease in fat mass. Female offspring showed decreased muscle mass alongside increased diabetes.
Seung Hyun Park et al, Paternal microplastic exposure alters sperm small non-coding RNAs and affects offspring metabolic health in mice, Journal of the Endocrine Society (2025). DOI: 10.1210/jendso/bvaf214
Why mangoes fall before they're ripe—and how science is helping them hang on
Why your mango tree drops fruit before it's ripe? Each season, mango growers across the world watch helplessly as millions of mangoes fall to the ground too early.
These mangoes never ripen properly, never reach consumers, and represent a major loss—both economically and environmentally. Premature fruit drop is a major contributor to low mango yields, with as little as 0.1% of fruits reaching maturity. This costs growers millions and wastes valuable resources. As climate stress intensifies, understanding why fruit is lost before harvest has global significance. It affects everything from food security to farm profitability.
Its sensitivity to environmental stress makes it vulnerable in a less predictable and more extreme climate. Drought, heat waves, and even leaf loss can influence a natural process that leads to fruit drop.
Just like humans, plants rely on hormonesto keep things growing and functioning smoothly.
These chemical messengers help regulate everything from flowering to fruit development.
But when plants experience stress, hormone levels shift. The plant starts reallocating resources to survive. Dropping fruit is often one of the first sacrifices.
One key resource that plants reallocate is carbohydrates. Developing fruit requires a steady supply of sugars, but under stress—such as leaf damage or water scarcity—the tree may struggle to produce or transport enough.
This can trigger fruit drop, as the plant prioritizes survival over reproduction.
Stress not only disrupts carbohydrate supply but also interferes with the hormonal balance in mango trees. This triggers what we call a molecular "quit signal": a message from the plant to let go of its fruit.
This signal is a part of a complex network of gene activity and hormonal cues that help the tree decide when to shed fruit.
Researchers are studying the molecular pathways behind this signal by analyzing gene signals from mango pedicel tissue—the stem that connects the fruit to the tree.
This tissue acts like a control center, managing the flow of nutrients and signals between the tree and the developing fruit. It's where the tree and fruit stay in touch, especially during stress.
By analyzing which genes are turned on or off, we can pinpoint the molecular signals involved in fruit drop, particularly those related to hormones.
This helps us move from just observing fruit drop to developing tools to control it.
One promising solution is the use of plant growth regulators, which are synthetic versions of plant hormones.
These can be applied to mango trees to help stabilize hormone levels during stressful conditions.
It's a bit like giving the tree a hormonal pep talk, encouraging it to hold onto fruit even when times are tough.
Applying plant growth regulators during flowering, before fruit has fully emerged, was more effective than applying them later in the season.
This early intervention helped reinforce the hormonal signals that support fruit retention. Initial trials have increased tree yield by up to 17%.
Even small-scale growers might one day use targeted treatments to help their trees hold on to fruit longer.
For consumers, reducing fruit drop means better access to fresh, affordable produce. For growers, it's about staying viable in an increasingly unpredictable climate. And for policymakers, it's about preparing the horticultural industry for the challenges ahead.
Importantly, fruit drop isn't unique to mangoes. Apples, citrus, and avocados also suffer losses due to hormonal imbalances triggered by environmental stress.
Better understanding the molecular mechanisms controlling fruit drop in mango, could benefit a wide range of fruit crops globally as the climate changes.
This article is republished from THE CONVERSATION under a Creative Commons license. Read the original article.
Dr. Krishna Kumari Challa
AI-designed antibodies race toward trials
Scientists say they are on the cusp of turning antibodies designed by artificial intelligence into potential therapies, just a year after they debuted the first example of an entirely AI-designed antibody. Previously, the structure of antibodies proved somewhat of a black box to AI models. But new and improved models — such as an updated version of AlphaFold — have more successfully predicted the shape of flexible structures that give antibodies the specificity they need to bind to foreign molecules. Researchers at several companies now say they’ve designed ‘drug-like’ antibodies.
https://www.nature.com/articles/d41586-025-03965-x?utm_source=Live+...
Dec 18, 2025
Dr. Krishna Kumari Challa
Scientists build a quantum computer that can repair itself using recycled atoms
Like their conventional counterparts, quantum computers can also break down. They can sometimes lose the atoms they manipulate to function, which can stop calculations dead in their tracks. But scientists have demonstrated a solution that allows a quantum computer to repair itself while it's still running.
The research team zeroed in on quantum computers that use neutral atoms (atoms with equal numbers of protons and electrons). These individual atoms are the qubits, or the basic building blocks of a quantum computer's memory. They are held in place by laser beams called optical tweezers, but the setup is not foolproof.
Occasionally, an atom slips out of its trap and disappears. When this happens mid-calculation, the whole process can grind to a halt because the computer can't function with a missing part.
In a paper published in the journal Physical Review X, the researchers detail how they solved this problem by rearranging the atoms within the machine. Instead of having all the atoms in a single crowded group, the team organized them into five distinct zones. This means that if an atom is lost in one part of the computer, the other qubits will not be affected.
The specialized zones are a "Register" for storing qubits, an "Interaction Zone" for performing calculations and a "Measurement zone" for checking errors using helper atoms known as "ancillas." There is also a "Storage Zone," a reservoir of spare atoms to replace those that are lost and a "Loading Zone' to bring in new atoms from the outside to refill the reservoir.
But the solution is even more sophisticated than that. This neutral atom-based quantum computer can detect a breakdown and fix it on the fly. When the system notices a missing qubit, it reaches into the storage zone and moves a new atom into place.
Once this atom is in position, the computer prepares it for work by resetting it to its ground state (lowest-energy state). The computer can also recycle the ancillas once they have performed their checks by resetting them in the same way.
To demonstrate that their solution works, the study authors had the computer run a repetition code, a process that checks its own work for mistakes. They ran these checks 41 times in a row, and each time, the machine successfully replaced its lost atoms without disturbing the data being processed. Without this self-repairing ability, the system would have run out of atoms after a few rounds.
J. A. Muniz et al, Repeated Ancilla Reuse for Logical Computation on a Neutral Atom Quantum Computer, Physical Review X (2025). DOI: 10.1103/v7ny-fg31
Dec 19, 2025
Dr. Krishna Kumari Challa
Life on lava: How microbes colonize new habitats
Life has a way of bouncing back, even after catastrophic events like forest fires or volcanic eruptions. While nature's resilience to natural disasters has long been recognized, not much is known about how organisms colonize brand-new habitats for the first time. A new study by a team of ecologists and planetary scientists provides glimpses into a poorly understood process.
The team conducted field research in Iceland following a series of eruptions of the Fagradalsfjall volcano, located on the southwestern tip of the island. The volcano erupted for a total of three times over the course of the study period, from 2021 until 2023. With each eruption, lava flows blanketed the tundra around the volcano, in some places even covering lava deposits from the previous year.
The lava coming out of the ground is over 2,000 degrees Fahrenheit, so obviously it is completely sterile. It's a clean slate that essentially provides a natural laboratory to understand how microbes are colonizing it.
To untangle the ecological dynamics involved in that process, the team searched for clues about where the microbes that colonize fresh lava come from. They collected samples from a variety of different potential sources, including lava that had solidified mere hours before, rainwater, and aerosols—particles floating in the air. For context, they sampled soil and rocks from surrounding areas.
The researchers then extracted DNA from these samples and used sophisticated statistical and machine learning techniques to identify the organisms present on freshly imposed lava flows, the composition of these micro-habitats and where they originated.
The work revealed that as microbes colonized the new habitat, biodiversity increased over the course of the first year following an eruption. But after the first winter, diversity "tanked', probably because the seasonal shifts in environmental conditions were selecting for a specific subset that could survive those conditions. With each subsequent winter, the analyses revealed less turnover and showed that diversity stabilized over time. With all these data, a picture began to emerge.
It appears that the first colonizers are these 'badass' microbes, for lack of a better term, the ones that can survive these initial conditions, the researchers say, "because there's not a lot of water and there's very little nutrients. Even when it rains, these rocks dry out really fast.
Over the next several months and seasonal shifts, the study revealed, the microbial community begins to stabilize, as more microbes are added with rainwater and "moved in" from adjacent areas.
Part 1
Dec 19, 2025
Dr. Krishna Kumari Challa
A major finding of the study pointed to rainwater playing a critical role in shaping microbial communities on freshly deposited lava, according to the researchers.
Early on, it appears colonizers are mostly coming from soil that is blown onto the lava surface, as well as aerosols being deposited. But later, after that winter shift in diversity they observed, they saw most of the microbes are coming from rainwater, and that's a pretty interesting result.
Scientists have long known that rainwater is not sterile; microbes in the atmosphere, either free floating or attached to dust particles, can even function as cloud condensation nuclei, which are microscopic particles that offer water vapor a surface to latch on to and grow into tiny droplets. In other words, tiny, invisible creatures may play outsized roles in weather and climate phenomena.
Nathan Hadland et al, Three eruptions at the Fagradalsfjall Volcano in Iceland show rapid and predictable microbial community establishment, Communications Biology (2025). DOI: 10.1038/s42003-025-09044-1
Part 2
Dec 19, 2025
Dr. Krishna Kumari Challa
Can 'miracle' heaters really warm your home for pennies? The physics says no
Claims that portable electric heaters can heat homes for pennies or rapidly warm entire houses are not supported by physics. All electric heaters are nearly 100% efficient, meaning almost all input electricity becomes heat, but this does not make them cheap to run. No plug-in heater can outperform others in efficiency or safely deliver enough power to heat a whole house quickly. Heat pumps offer greater efficiency by moving heat rather than generating it, but are costly to install. Effective home heating relies on better insulation, efficient systems, and affordable energy, not miracle devices.
Dec 19, 2025
Dr. Krishna Kumari Challa
Urban birds' beak shape rapidly changed during COVID-19 lockdowns, suggesting human-driven transformations
During the COVID-19 lockdowns, urban dark-eyed juncos developed longer, thinner beaks resembling their wild counterparts, likely due to reduced human food waste. As human activity resumed, beak shapes reverted to the shorter, thicker form typical of urban birds. These rapid, reversible changes highlight the strong influence of human presence on urban bird morphology.
When the world slowed down during the COVID-19 pandemic, its effects extended beyond humans. A recent study found that it reshaped urban ecosystems to such an extent that certain city-dwelling birds even began to develop longer, thinner beaks resembling those of their wild relatives.
The dark-eyed junco is a small, grayish songbird that is a common winter guest across North America.
A research duo from the University of California, Los Angeles, identified that the juncos living on campus were an ideal system for exploring how physical traits change in urban environments. They tracked changes in the birds across the pre-pandemic and post-pandemic periods, from 2018 to 2025.
They observed that birds that hatched during the pandemic, when the campuses became empty and there was less food waste to feed on, had beaks with higher bill length and slimmer structure, similar to the wildland birds. However, after the COVID-19 restrictions were lifted and people started trickling back to campus and food waste became ample. Birds born during this period reflected this shift, exhibiting shorter, thicker beaks typical of urban juncos.
Studies have shown that animals living in cities can undergo rapid phenotypic changes — observable alterations in an organism's traits or characteristics—in response to newer environments, necessary to increase their chances of survival and the urban setting.
The juncos living in California, U.S. are no longer winter visitors, they have become year-round residents over the past few decades. As a result, these birds appear to have adapted to urban life by evolving physical traits that help them thrive in city landscapes.
One of the most striking changes is in their beaks. Juncos living in Los Angeles have shorter, thicker beaks than those found in local mountainous forests. Scientists think that this change might be linked to their diet, which now includes human food waste rather than the seeds, worms, and insects that wild juncos typically eat.
The period of global slowdown caused by COVID-19 lockdowns, now known as the anthropause, gave scientists a rare chance to see how animals physically changed when human activity suddenly decreased.
Part1
Dec 19, 2025
Dr. Krishna Kumari Challa
the researchers found that the anthropause corresponded with changes in bill shape and size. Birds hatched during the pandemic had beaks similar to wild juncos, but as human activity picked up again, their beaks reverted to the short, stout form seen in urban populations. These results indicate that city birds quickly adjusted their behavior when human activity stopped and started again.
The researchers note that further genetic and behavioral studies in both urban and wildland populations are needed to confirm whether these shifts were driven by genetic changes triggered by low human activity or temporary movements of wild birds into the city during the pandemic.
Eleanor S. Diamant et al, Rapid morphological change in an urban bird due to COVID-19 restrictions, Proceedings of the National Academy of Sciences (2025). DOI: 10.1073/pnas.2520996122
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Part 2
Dec 19, 2025
Dr. Krishna Kumari Challa
Mitochondria migrate toward the cell membrane in response to high glucose levels, study shows
In pancreatic beta cells, high glucose levels cause mitochondria to migrate toward the cell periphery. This movement depends on intact microtubules and cAMP signaling, but not on mitochondrial ATP production. Peripheral redistribution of mitochondria may influence insulin secretion, suggesting spatial organization of mitochondria is important for beta cell function.
Mitochondrial position responds to glucose stimulation in a model of the pancreatic beta cell, Biophysical Journal (2025). DOI: 10.1016/j.bpj.2025.11.018. www.cell.com/biophysj/fulltext … 0006-3495(25)00767-2
Dec 19, 2025
Dr. Krishna Kumari Challa
Bacterium hijacks fruit ripening program in citrus plants to steal sugars, research reveals
Xanthomonas citri, the causative agent of citrus canker, manipulates citrus leaf cells by activating a fruit ripening program, leading to the release of cell wall-bound sugars that fuel rapid bacterial growth. This process mimics natural fruit ripening at the genetic level and highlights a mechanism by which pathogens access otherwise inaccessible nutrients, offering potential strategies for developing disease-resistant citrus varieties.
Trang Thi-Thu Phan et al, Xanthomonas coordinates type III–type II effector synergy by activating fruit-ripening pathway, Science (2025). DOI: 10.1126/science.adz9239
Dec 19, 2025
Dr. Krishna Kumari Challa
Is aging an act of genetic sabotage? Scientists find a gene that turns off food detection after reproduction
A gene called nhr-76 in roundworms actively suppresses food-odor detection after reproduction by switching off related sensory genes in neurons. This programmed decline, rather than accumulated damage, suggests aging can involve active genetic regulation. Similar genes in mammals may play related roles, but their effects in humans remain unconfirmed.
Rikuou Yokosawa et al, A Nuclear Hormone Receptor nhr‐76 Induces Age‐Dependent Chemotaxis Decline in C. elegans, Aging Cell (2025). DOI: 10.1111/acel.70277
Dec 19, 2025
Dr. Krishna Kumari Challa
Global food systems driving twin crises of obesity and global warming, says review
Unsustainable, profit-driven food systems promote high-calorie, low-fiber diets, contributing to rising obesity and significant greenhouse gas emissions. Animal-based and ultra-processed foods are key drivers of both health and environmental harms. System-level reforms—such as taxes, subsidies, and marketing restrictions—are recommended to improve diets and reduce climate impact.
A major review in Frontiers in Science highlights how tackling unsustainable food systems—reflected by our changing food environment—is urgent for both health and climate.
The paper reviews evidence that both obesity and environmental harms result from a profit-led food system that encourages high intake and poor health. The authors say that our food environment promotes high-calorie, low-fiber products such as some ultra-processed foods (UPFs)—the most caloric of which encourage weight gain.
Those same production systems, especially involving animals, release large amounts of greenhouse gases and put pressure on land and water.
The comprehensive review says that addressing the food environment can therefore deliver double benefits for health and climate.
The authors recommend using subsidies for healthy foods, taxes and warning labels for particularly unhealthy foods, and restrictions on aggressive marketing of high-calorie, low-fiber products, particularly in low-income communities and to children.
They also counter the perception that weight-loss drugs are a panacea for obesity, as they do not address the systemic drivers which also harm the climate.
Obesity and climate change: co-crises with common solutions, Frontiers in Science (2025). DOI: 10.3389/fsci.2025.1613595
Dec 19, 2025
Dr. Krishna Kumari Challa
Antifungal vaccine heads for clinical trials
A vaccine designed to protect against infections with certain fungal pathogens is set to move into phase I clinical trials, backed by US$40 million in funding from the US National Institutes of Health. The vaccine, called VXV-01, uses two antigens to elicit an immune response to fungal pathogens such as Candida auris and Candida albicans, which can cause drug-resistant infections in hospitals.
https://www.genengnews.com/topics/infectious-diseases/fungal-vaccin...
Dec 19, 2025
Dr. Krishna Kumari Challa
The Roots of Dementia in Childhood
Dementia is often associated with older people, but it doesn't just appear out of nowhere.
Some risk factors could start before we're even born, while others emerge as we progress through childhood into young adulthood.
According to research, that could be the best time to start intervention.
Even before we are born, some risk factors for dementia may already be present.
Increasingly, evidence suggests that the roots of age-related cognitive decline could begin in early childhood.
One of the most important factors explaining cognitive ability at age 70, researchers say, is cognitive ability at age 11.
Later, in early adulthood, additional potential risk factors include:
Education
Head injuries
Physical activity
Social isolation
Growing up healthy could be key to growing old healthy.
https://academic.oup.com/psychsocgerontology/article/78/12/2131/728...
https://www.sciencealert.com/the-roots-of-dementia-trace-back-all-t...**
Dec 19, 2025
Dr. Krishna Kumari Challa
Quantum computers have memory problems over time
A team of international scientists has, for the first time, created a full picture of how errors unfold over time inside a quantum computer—a breakthrough that could help make future quantum machines far more reliable.
The researchers found that the tiny errors that plague quantum computers don't just appear randomly. Instead, they can linger, evolve and even link together across different moments in time.
The team has made its experimental data and code openly available, and the full study is published in Quantum.
This type of behavior is one of the key obstacles to building practical, large-scale quantum computers.
The team ran a series of experiments on cutting-edge superconducting quantum processors—some in the lab at the University of Queensland and others accessed through IBM's cloud-based quantum computers.
Previous attempts to map the behaviour of quantum systems over time all hit the same roadblock: after measuring a quantum system mid-experiment, scientists couldn't freely set it up again for the next step, because the setting-up depends on whether the result of the measurement was 0 or 1.
The new method solves this by adding a clever twist, assuming that 50% of the time, the result was 1, and the remaining time, the result was 0. Then, the researchers used software to work backwards with the data, to figure out what state it was in.
What they found is that even today's best quantum machines show subtle but important time-linked noise patterns—including noise that is quantum in nature and comes from nearby qubits on the same chip.
Understanding these patterns will help quantum scientists design better characterization and error-correction tools, a crucial step toward building dependable, fault-tolerant quantum computers.
Multi-time quantum process tomography on a superconducting qubit, Quantum (2025). DOI: 10.22331/q-2025-12-02-1582
Dec 20, 2025
Dr. Krishna Kumari Challa
Ancient viral DNA shapes early embryonic development
A new study reveals how ancient viral DNA once written off as "junk" plays a crucial role in the earliest moments of life. The research, published in Science Advances, begins to untangle the role of an ancient viral DNA element called MERVL in mouse embryonic development and provides new insights into a human muscle wasting disease.
Transposable elements are stretches of DNA that can move around the genome. Many of these DNA sequences originate from long ago, when viruses inserted their genetic material into our ancestors' genomes during infection. Today, these viral transposable elements make up around 8-10% of the mammalian genome.
Once disregarded as "junk" DNA, we now know that many transposable elements play an important role in influencing how genes are turned on and off, especially during early development. They have a variety of beneficial and harmful roles in the body, for example, some help regulate normal immune responses, while others can disrupt genes and contribute to diseases like cancer.
The latest work focuses on a viral transposable element called MERVL.
This element becomes highly active for a short window of time when a mouse embryo reaches the two-cell stage—the point at which a fertilized egg has divided into two cells and switches on its own genome for the first time. Cells in this state are considered "totipotent," meaning they can generate every cell type of the embryo and extraembryonic tissues like the placenta.
MERVL acts as a central switch to activate a large network of genes specific to the two-cell stage of development.
To work out the role of MERVL, the team used a gene manipulation technique called CRISPR activation to turn on MERVL elements in mouse embryonic stem cells, to mimic what happens in two-cell embryos.
In cells where only MERVL was activated, the cells looked like they were only partially similar to cells of the two-cell stage, but they still had several characteristics of totipotency. The researchers described this in-between state as an "intermediate phenotype." They showed that activating MERVL alone is sufficient to create totipotent features in early embryonic development.
Paul Chammas et al, CRISPRa-mediated disentanglement of the Dux-MERVL axis in the 2C-like state, totipotency and cell death, Science Advances (2025). DOI: 10.1126/sciadv.adu9092. www.science.org/doi/10.1126/sciadv.adu9092
Dec 20, 2025
Dr. Krishna Kumari Challa
New 'cloaking device' concept shields electronics from disruptive magnetic fields
Unwanted magnetic fields can disrupt the operation of precision instruments, sensors, and electronic components, leading to signal distortion, data errors, or equipment malfunction. This is a growing concern in environments such as hospitals, power grids, aerospace systems, and scientific laboratories, where increasingly sensitive technologies require effective protection from magnetic interference.
Researchers have unveiled a concept for a device designed to magnetically "cloak" sensitive components, making them invisible to detection.
A magnetic cloak is a device that hides or shields an object from external magnetic fields by manipulating how these flow around an object so that they behave as if the object isn't there.
In Science Advances, the team of engineers demonstrate for the first time that practical cloaks can be engineered using superconductors and soft ferromagnets in forms that can be manufactured.
Using computational and theoretical techniques such as advanced mathematical modeling and high-performance simulations based on real-world parameters, they have developed a new physics-informed design framework that allows magnetic cloaks to be created for objects of any shape. Until now, cloaks were mostly theoretical or restricted to simple shapes like cylinders.
This study demonstrates for the first time how to design magnetic cloaks for the irregular geometries we see in the real world. These cloaks also maintain their effectiveness across a broad range of field strengths and frequencies.
Magnetic cloaks could play a vital role in protecting sensitive electronics and sensors from magnetic interference, which is a growing challenge in everything from medical devices to renewable energy and space technology.
Yusen Guo et al, Designing Functional Magnetic Cloaks for Real-World Geometries, Science Advances (2025). DOI: 10.1126/sciadv.aea2468. www.science.org/doi/10.1126/sciadv.aea2468
Dec 20, 2025
Dr. Krishna Kumari Challa
Biophysicists uncover new electrical transmission in cells
Many biological processes are regulated by electricity—from nerve impulses to heartbeats to the movement of molecules in and out of cells.
A new study by search scientists reveals a previously unknown potential regulator of this bioelectricity: droplet-like structures called condensates. Condensates are better known for their role in compartmentalizing the cell, but this study shows they can also act as tiny biological batteries that charge the cell membrane from within.
The team showed that when electrically charged condensates collide with cell membranes, they change the cell membrane's voltage—which influences the amount of electrical charge flowing across the membrane—at the point of contact.
The discovery, published in the journal Small, highlights a new fundamental feature about how our cells work, and could one day help scientists treat certain diseases.
Condensates are organelles—structures within cells that carry out specific functions—but unlike more well-known organelles such as the nucleus and mitochondria, they are not enclosed within membranes. Instead, condensates are held together by a combination of molecular and electrical forces. They also occur outside of cells, such as at neuronal synapses.
Condensates are involved in many essential biological processes, including compartmentalizing cells, protein assembly and signaling both within and between cells. Previous studies have also shown that condensates carry electrical charges on their surfaces, but little is known about how their electrical properties relate to cellular functions.
If condensates can alter the electrical properties of cell membranes, it could have big implications, because many cellular processes are controlled by changes in the cell membrane voltage. For example, ion channels—proteins that rapidly transport molecules across the cell membrane—are activated by changes in cell membrane voltage.
In the nervous system, this rapid, one-directional transport of electrically charged molecules is what drives the propagation of electrical signals between nerves.
Part 1
Dec 20, 2025
Dr. Krishna Kumari Challa
To test whether condensates can alter cell membrane voltage, the researchers used cell models called Giant Unilamellar Vesicles (GUVs). To allow them to visualize changes in voltage, they stained GUV membranes with a dye that changes color in response to changes in electrical charge. Then, they put GUVs in the same vessel as lab-made condensates and photographed their interactions under the microscope.
They showed that when the condensates and GUVs collided, it caused a local change in the GUV membranes' electrical charge at their point of contact.
By varying the chemical makeup of the condensates, the researchers showed that the more electrical charge a condensate carried, the bigger its impact on cell membrane voltage. They also found that the shape of the condensates appeared to be correlated with variations in the voltage change.
In some instances, the voltages induced are quite substantial in magnitude—on the same scale as voltage changes in nerve impulses.
Anthony Gurunian et al, Biomolecular Condensates Can Induce Local Membrane Potentials, Small (2025). DOI: 10.1002/smll.202509591
Part 2
Dec 20, 2025
Dr. Krishna Kumari Challa
Earth's Seasons Are Strangely Out of Sync, Scientists Discover From Space
Scientists have watched our planet's seasons from space and discovered that spring, summer, winter, and fall are surprisingly out of sync.
Just because two places exist in the same hemisphere, at similar altitudes, or at the same latitude doesn't guarantee they'll experience the same seasonal changes at the same time.
Even regions that are side by side can experience different weather and ecological patterns, sculpting wildly different neighboring habitats.
It's similar to how time zones can separate two adjacent spots, but in this case, the boundary is drawn by nature itself.
Using 20 years of satellite data, researchers have created what they say is the most comprehensive map to date of the seasonal timing of Earth's terrestrial ecosystems.
The new map identifies global regions where seasonal patterns are particularly out of sync, and these asynchronies often occur in biodiversity hotspots.
That is probably no coincidence. More variability in weather patterns can have trickle-down effects, which may drive greater diversity within habitats.
For example, if natural resources in two neighboring habitats are made available at different times of the year, it could shape the ecology and evolution of flora and fauna in each spot.
It could even mean that a species in one habitat reaches its reproductive season before or after the same species in an adjacent habitat, preventing interbreeding.
Across many generations, this can lead to the evolution of two entirely separate species.
https://www.nature.com/articles/s41586-025-09410-3
Dec 21, 2025
Dr. Krishna Kumari Challa
Holes in your colon!
Part 1Dec 21, 2025
Dr. Krishna Kumari Challa
Most People Develop Diverticulosis in Their Gut by Age 80
It's easy to see your body aging on the outside – wrinkles, dark spots, gray hair, the whole shebang – but as we grow older, our insides also inevitably change.By the time most people reach the ripe age of 80, the smooth lining of their digestive tract is scattered with small, bulging pouches of tissue.
These sac-like protrusions along the digestive tract, called diverticula, are 'weak spots' in the gut's muscular wall. They are typically harmless, and most people never even know they are there.
Sometimes, after a colonoscopy, patients are alarmed to find they have developed diverticulosis, but most of the time, this condition is nothing to worry about.
Only if the pouches become inflamed or infected is it considered diverticular disease, or diverticulitis. Symptoms, which generally come and go, often include constipation, diarrhea, abdominal pain, bloating, or fever.
The good news is that even if a person does develop diverticulitis, their symptoms usually improve with just a few days of bed rest and a liquid diet. Over 85 percent of patients find this sufficient.
No one knows exactly what causes diverticula to form in the first place, but current treatments generally focus on helping the digestive tract move smoothly, without blockages.
That's why a high-fiber diet, including between 25 and 30 grams of fiber a day, is often recommended to recovering patients. This won't heal existing diverticula, but may prevent more from forming.
Other potential risk factors include obesity, lack of exercise, and smoking. There's likely a complicated mix of contributing factors.
Part2
Dec 21, 2025
Dr. Krishna Kumari Challa
While diverticula can develop in the large and small intestine, around 95 percent of patients in the Western world have diverticula in their sigmoid colon.
This part of the digestive tract works under great pressure to push feces into the rectum.
Once diverticula form, possibly from excessive pressure, they are prone to bleeding when aggravated, in a similar way to hemorrhoids, which form inside and outside the rectum and around the anus.
Diverticular bleeding is estimated to cause between 30 and 65 percent of all cases of lower gastrointestinal bleeding. It's usually painless and self-limiting, but seeing blood in the stool is a serious matter, as it may indicate other severe conditions.
Treatment depends on the severity of the episode.
https://www.sciencealert.com/most-people-develop-diverticulosis-in-...
Part 3
Dec 21, 2025
Dr. Krishna Kumari Challa
2.8 days to disaster: Why we are running out of time in low earth orbit
Satellite mega-constellations in low Earth orbit experience close approaches every 22 seconds, with each satellite performing frequent avoidance maneuvers. Solar storms increase atmospheric drag and can disable satellite control systems, raising collision risks. If operators lose control, a catastrophic collision could occur within 2.8 days, compared to 121 days in 2018, highlighting increased vulnerability.
Sarah Thiele et al, An Orbital House of Cards: Frequent Megaconstellation Close Conjunctions, arXiv (2025). DOI: 10.48550/arxiv.2512.09643
Dec 21, 2025
Dr. Krishna Kumari Challa
Physicists crack a 'Big Bang Theory' problem that could help explain dark matter
Theoretical work demonstrates that axions, hypothetical particles considered a candidate for dark matter, could be produced in fusion reactors using deuterium, tritium, and lithium. Neutron interactions with reactor walls and bremsstrahlung processes may generate axions or axion-like particles, offering a new approach to probing dark matter beyond solar-based searches.
Chaja Baruch et al, Searching for exotic scalars at fusion reactors, Journal of High Energy Physics (2025). DOI: 10.1007/jhep10(2025)215
Dec 21, 2025
Dr. Krishna Kumari Challa
The moon-forming event: Why it was by explosive ejection rather than a giant impact
A new model proposes that the Moon formed from explosive ejection of Earth's mantle and crust, driven by accumulated internal gravitational energy (LɅ) released at the core-mantle boundary, rather than by a giant impact. This mechanism explains the Moon's isotopic similarity to Earth and links geophysical processes, such as mantle plumes and LLVPs, to lunar formation.
Matthew R. Edwards, Explosive lunar fission above a large low-velocity province, Acta Geochimica (2025). DOI: 10.1007/s11631-025-00834-2
Dec 21, 2025
Dr. Krishna Kumari Challa
Scientists observe 'extraordinary' seven-arm octopus
A rare deep-sea encounter captured footage of the seven-arm octopus, Haliphron atlanticus, at 700 meters depth in Monterey Bay. This species, with females reaching up to 4 m and 75 kg, primarily inhabits the ocean's twilight zone and feeds on gelatinous animals such as jellyfish, supporting previous observations of its unusual diet.
Hoving, H.J.T. and S.H.D. Haddock. 2017. The giant deep-sea octopus Haliphron atlanticus forages on gelatinous fauna. Scientific Reports, 7: 44952. https://doi.org/10.1038/srep44952
Dec 21, 2025
Dr. Krishna Kumari Challa
Natural daylight can help people with diabetes improve blood sugar levels
People with type 2 diabetes may be able to improve their blood sugar by doing something as simple as sitting by a window for a few hours each day. In a study published in Cell Metabolism, scientists showed that natural daylight helps maintain healthy glucose levels.
Daylight is known to be a mood enhancer and also beneficial for our health. However, according to the research team, most people living in Western societies typically stay indoors around 80% to 90% of the time under artificial light, which is not as bright or dynamic as sunlight. This is important because the human body operates on circadian rhythms, internal 24-hour clocks that orchestrate a range of biological processes, such as digestion and temperature regulation. These are synchronized by light, and a lack of natural light is a risk factor for type 2 diabetes.
Previous studies have shown that artificial light at night disrupts these rhythms and that daylight outdoors can improve the body's response to insulin, which helps control blood sugar levels. But no prior research examined how natural light entering a window affects people with diabetes.
To test this, researchers recruited 13 volunteers with type 2 diabetes to examine how their bodies responded to both natural window lighting and artificial indoor lighting. The participants spent two separate 4.5-day periods in a controlled office environment. In one session, they sat at a desk facing large windows from morning to late afternoon.
In the other, they were in the same room, with the windows blocked and only standard office lights. All participants ate similar meals three times a day and performed the same exercises at the same time across the two sessions. They also continued taking their medication.
The results revealed that while average glucose levels were similar across the two sessions, the participants spent significantly more time in the normal glucose range when exposed to natural daylight. The body's metabolism also changed. In daylight, the volunteers burned more fat for energy and fewer carbohydrates.
The researchers also took muscle biopsies and grew muscle cells in the lab. They found that genes involved in their internal cellular clocks were better aligned to the time of day under natural light. This suggested that sunlight was acting as a signal to keep the muscles "on time," making them better at processing nutrients.
Although this study involved only a handful of people, the results indicate that natural daylight can help reduce the sharp peaks and swings in blood sugar that often affect those with this condition. It offers a simple, natural way to support people with type 2 diabetes alongside existing treatments.
Jan-Frieder Harmsen et al, Natural daylight during office hours improves glucose control and whole-body substrate metabolism, Cell Metabolism (2025). DOI: 10.1016/j.cmet.2025.11.006
Dec 23, 2025
Dr. Krishna Kumari Challa
Scientists who use AI tools are publishing more papers than ever before
Science is entering a massive publishing boom, in large part due to artificial intelligence. New research published in the journal Science has revealed that scientists who use large language models (LLMs) like ChatGPT are producing significantly more papers across many fields. The technology is also helping to level the playing field for researchers whose first language isn't English.
The growing use of AI in scientific research has sparked concerns about shoddy work and machines making things up. But this new analysis also reveals that papers produced with LLMs use more complex language and cite a wider array of sources.
They found that when scientists use AI, their productivity soared. The biggest jump was in the social sciences and humanities, where output increased by 59.8%, while biology and life sciences saw a 52.9% increase. Meanwhile, in physics and math, the scientists report a 36.2% boost. "LLM adoption is associated with a large increase in researchers' scientific output," wrote the research team in their paper.
One of the most fascinating findings was the massive increase in productivity from non-English-speaking countries. Most top journals require manuscripts to be written in high-level English, which has long disadvantaged these scientists. But with AI handling some of the workload, researchers from Asia saw their output jump by as much as 89% in some cases.
However, the study authors also issued a warning regarding AI and quality. While the machines can make papers sound more professional, this can be a trap. Historically, sophisticated writing was a sign of high-quality research, but now the opposite can sometimes be true. The study found that the more complex the AI-generated writing was, the less likely the paper was to be high quality. In other words, good writing can mask weak ideas.
The clear message from the study authors is that we can no longer judge a paper by how smart the language appears. "As traditional heuristics break down, editors and reviewers may increasingly rely on status markers such as author pedigree and institutional affiliation as signals of quality, ironically counteracting the democratizing effects of LLMs on scientific production."
To safeguard scientific integrity, the researchers propose several measures, including that institutions implement deeper checks and even specialized "AI-based reviewer agents" to help distinguish between human writing and machine-generated writing.
Keigo Kusumegi et al, Scientific production in the era of large language models, Science (2025). DOI: 10.1126/science.adw3000
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Dec 23, 2025
Dr. Krishna Kumari Challa
How chirality goes from the molecular level to the cellular one
Researchers have discovered how right-handed molecules in our cells can give rise to cells that are not symmetrical about their central axes. This discovery is a key step toward determining why most of our organs lack left–right symmetry.
It's conceivable that if some molecules that make up our cells were twisted in the opposite direction, our hearts would be on the right side of our bodies rather than on the left.
That's because the difference between the left and right sides of our organs may originate from the "handedness," or chirality, of cells, which in turn comes from the chirality of molecules in cells.
However, the link between the chirality of molecules and cellular chirality is largely unknown. Many molecules in cells are chiral, including DNA and some amino acids and proteins, but it's not clear which ones convey their chirality to cells.
By studying the chiral behaviours of individual cells, researchers have found that the cells' scaffolding, or cytoskeleton, gives rise to the cell's chirality. The findings are published in the journal eLife.
When single cells were placed on a substrate, their nuclei and surrounding cytoplasm rotated in a clockwise direction when viewed from above. This rotational motion is driven by the concentric pattern of the actomyosin filaments that make up the cytoskeleton.
This finding implies that the cell nucleus can rotate even when there is no chiral orientation of the cytoskeleton on a cellular level.
To confirm whether this mechanism was driving the rotation, the team created a 3D theoretical model of a cell and evaluated the effect of the molecular chirality of actin and myosin on it. The results revealed that the molecular scale torque generated by individual components of the cytoskeleton can generate rotation, even when cell-level chiral structures were absent.
These results help fill in a critical link in the chain from molecules to organs and bodies, the researchers say.
Takaki Yamamoto et al, Epithelial cell chirality emerges through the dynamic concentric pattern of actomyosin cytoskeleton, eLife (2025). DOI: 10.7554/elife.102296
Dec 23, 2025
Dr. Krishna Kumari Challa
PFAS concentrations can double with every step up the food chain
PFAS concentrations increase twofold on average with each step up the food chain, resulting in significantly higher levels in top predators and humans. Analysis of 119 global food webs shows substantial variation among PFAS compounds, with some newer alternatives magnifying even more than legacy chemicals. These findings highlight the need for compound-specific regulation and further research into health impacts.
The authors examined 119 aquatic and terrestrial food webs across the globe, finding that top predators such as large fish, seabirds, and marine mammals can accumulate PFAS concentrations exponentially larger than the environments in which they're found. The study is published in the journal Nature Communications.
PFAS concentrations double, on average, with each step up the food chain.
Known as "forever chemicals," PFAS are from a family of more than 12,000 man-made compounds.
These chemicals are prized for their heat resistance and water-repelling properties, and are used in cleaning products, food packaging, non-stick pans, clothing, and fire-fighting equipment.
Since being discovered by the American chemical company DuPont in the 1930s, PFAS are now detectable in the bloodstream of almost every human being on the planet.
Unlike other chemicals, PFAS never break down, meaning that throughout the world right now, they're building up in environments, plants, and animals on land and in the ocean.
For humans, sitting as we do at the top of the food chain, this means our diets can be an important pathway for PFAS exposure.
Given what we know about PFAS toxicity from other studies, these extreme accumulation rates in top predators suggest serious health risks. This creates a cascading ecological risk: Apex predators face disproportionately high exposure even in relatively low-contaminated environments.
Some compounds—including chemicals marketed as safer alternatives to existing products—showed even higher magnification than the chemicals they were designed to replace.
Lorenzo Ricolfi et al, Unravelling the magnitude and drivers of PFAS trophic magnification: a meta-analysis, Nature Communications (2025). DOI: 10.1038/s41467-025-65746-4
Dec 23, 2025
Dr. Krishna Kumari Challa
More eyes on the skies can help planes reduce climate-warming contrails
Aviation's climate impact is partly due to contrails—condensation that a plane streaks across the sky when it flies through icy and humid layers of the atmosphere. Contrails trap heat that radiates from the planet's surface, and while the magnitude of this impact is uncertain, several studies suggest contrails may be responsible for about half of aviation's climate impact.
Geostationary satellites detect only about 20% of contrails visible to low-Earth-orbiting satellites, primarily missing smaller, younger contrails. Combining data from geostationary, low-Earth-orbit, and ground-based observations can provide a more complete understanding of contrail formation and evolution, supporting more effective contrail avoidance strategies to mitigate aviation's climate impact.
Pilots could conceivably reduce their planes' climate impact by avoiding contrail-prone regions, similarly to making altitude adjustments to avoid turbulence. But to do so requires knowing where in the sky contrails are likely to form.
To make these predictions, scientists are studying images of contrails that have formed in the past. Images taken by geostationary satellites are one of the main tools scientists use to develop contrail identification and avoidance systems.
But a new study shows there are limits to what geostationary satellites can see.
Researchers analyzed contrail images taken with geostationary satellites, and compared them with images of the same areas taken by low-Earth-orbiting (LEO) satellites. LEO satellites orbit Earth at lower altitudes and therefore can capture more detail. However, since LEO satellites only snap an image as they fly by, they capture images of the same area far less frequently than geostationary (GEO) satellites, which continuously image the same region of Earth every few minutes.
The researchers found that geostationary satellites miss about 80% of the contrails that appear in LEO imagery. Geostationary satellites mainly see larger contrails that have had time to grow and spread across the atmosphere. The many more contrails that LEO satellites can pick up are often shorter and thinner. These finer threads likely formed immediately from a plane's engines and are still too small or otherwise not distinct enough for geostationary satellites to discern. The study highlights the need for a multiobservational approach in developing contrail identification and avoidance systems. The researchers emphasize that both GEO and LEO satellite images have their strengths and limitations.
Observations from both sources, as well as images taken from the ground, could provide a more complete picture of contrails and how they evolve.
With more 'eyes' on the sky, we could start to see what a contrail's life looks like, the researchers conclude.
Marlene V. Euchenhofer et al, Contrail Observation Limitations Using Geostationary Satellites, Geophysical Research Letters (2025). DOI: 10.1029/2025gl118386
Dec 23, 2025
Dr. Krishna Kumari Challa
Biodegradable electronics can break down into harmful microplastics
Some materials used in biodegradable electronics, such as PEDOT:PSS, can persist for years and degrade into microplastics, raising environmental concerns. In contrast, polymers like cellulose and silk fibroin degrade more safely. The environmental impact of both material choice and manufacturing processes is significant, highlighting the need for sustainable, circular approaches in electronics production.
Sofia Sandhu et al, End-of-Life usefulness of degradation by products from transient electronics, npj Flexible Electronics (2025). DOI: 10.1038/s41528-025-00411-w
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Dec 23, 2025
Dr. Krishna Kumari Challa
People are getting their news from AI—and it's altering their views
Large language models increasingly shape public opinion by generating news content and summaries, often introducing subtle communication bias by emphasizing certain viewpoints while minimizing others, even when information is accurate. This bias stems from model design, training data, and market concentration. Current regulations focus on harmful outputs but are less effective against nuanced framing biases, highlighting the need for greater competition, transparency, and user involvement.
Read the original article.
Dec 23, 2025
Dr. Krishna Kumari Challa
Scientists chart over 140,000 DNA loops to map human chromosomes in the nucleus
Over 140,000 DNA looping interactions were mapped in human embryonic stem cells and fibroblasts, providing a detailed 3D organization of chromosomes within the nucleus. Computational models now predict genome folding from DNA sequence alone, clarifying how chromatin loops influence gene regulation and how genetic variations may alter genome structure and function.
Job Dekker et al, An integrated view of the structure and function of the human 4D nucleome, Nature (2025). DOI: 10.1038/s41586-025-09890-3
Elzo de Wit, Systematic maps reveal how human chromosomes are organized, Nature (2025). DOI: 10.1038/d41586-025-03808-9
Dec 23, 2025
Dr. Krishna Kumari Challa
Two ancient human species came out of Africa together, not one, suggests new study
The textbook version of the "Out of Africa" hypothesis holds that the first human species to leave the continent around 1.8 million years ago was Homo erectus. But in recent years, a debate has emerged suggesting it wasn't a single species, but several. New research published in the journal PLOS One now hopes to settle the matter once and for all.
The debate centers on the Dmanisi fossils, five skulls found in the Republic of Georgia between 1999 and 2005, which belong to some of the oldest humans ever found outside Africa. The problem is that they don't look alike. Some are larger than others, particularly Skull 5, which has a tiny braincase but a massive, protruding face. Some researchers explain this as a difference in sexes within the same species, while others argue that it represents two distinct species living together.
To provide much-needed clarity, researchers studied the teeth of three Dmanisi specimens. The reason is that, generally, skulls are not always the best species identifiers because bone is fragile and can be warped and crushed. Dentition is far more useful because enamel is the hardest biological substance produced by humans, and everything from the shape and size of individual teeth can be used to identify a species.
The team focused on the surface area (dental crown) of the back teeth (premolars and molars) of the Dmanisi specimens that had sufficient dental remains for analysis. They compared these to a database of 122 other fossil specimens, including Australopithecus and several other Homo species. Then, using a statistical sorting tool, they analyzed 583 teeth to create a biological map and determine whether the Dmanisi fossils belonged to a single family or to other branches of our family tree.
The map revealed that these ancient remains were not from a single group. Skull 5, with its large jaw, was grouped with Australopiths, a more primitive ape-like ancestor. The other two specimens were more human-like. Because of this, the study authors support using the names Homo georgicus for Skull 5 and Homo caucasi for the human-like group.To ensure the differences weren't just between males and females, the team compared the fossils with those of great apes. In some animals, like gorillas, males are much larger than females but still have the same basic teeth. The differences between the Dmanisi teeth were so great that male-female differences within the same group couldn't explain them.
Part 1
Dec 23, 2025
Dr. Krishna Kumari Challa
The postcanine dental crown area analysis of the Dmanisi hominin fossils... supports the hypothesis of distinct species coexisting temporally at the site (Homo caucasi and Homo georgicus). This possibility challenges the prevailing model of Homo erectus migration out of Africa..." commented the researchers in their paper.
While the research lends weight to the idea that two species left Africa at roughly the same time, more specimens may be needed before a consensus is reached.
Victor Nery et al, Testing the taxonomy of Dmanisi hominin fossils through dental crown area, PLOS One (2025). DOI: 10.1371/journal.pone.0336484
Part 2
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Dec 23, 2025
Dr. Krishna Kumari Challa
Some mammals can hit pause on a pregnancy—understanding how that happens could help us treat cancer
Embryonic diapause allows some mammals to pause development by activating a molecular brake that suppresses differentiation pathways, maintaining stem cell pluripotency during metabolic stress. This mechanism involves the displacement of Capicua, enabling genes that inhibit the MAP kinase pathway. The findings suggest similar dormancy programs may underlie long-term survival in immune, stem, and cancer cells.
Tuo Zhang et al, Transcriptional derepression of negative regulators of MAP kinase supports maintenance of diapause ES cells in the pluripotent state, Genes & Development (2025). DOI: 10.1101/gad.353143.125
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Dec 23, 2025
Dr. Krishna Kumari Challa
Dec 23, 2025
Dr. Krishna Kumari Challa
Whale, dolphin strandings show widespread disease, trauma
Analysis of 272 cetacean strandings in the Pacific Islands from 2006 to 2024 found that over 65% involved disease or human-caused trauma. Disease accounted for 62% of cases, with infectious agents like morbillivirus and brucella affecting multiple species. Human-related trauma, including vessel strikes and debris ingestion, contributed to 29% of strandings.
From land-borne pathogens to high-speed vessel strikes, Pacific whales and dolphins are caught in a "perfect storm" where human-caused trauma and infectious diseases were found in more than 65% of investigated strandings.
A study spanning nearly two decades by researchers provides insights into the threats whales and dolphins face in the Pacific Islands.
Based on 272 stranding investigations of 20 cetacean species between 2006 and 2024, the study provides foundational data to better manage and conserve Hawaiʻi's whales and dolphins. The findings are published in the journal Diseases of Aquatic Organisms.
Over 18 years, scientists examined more than three-quarters of the stranded whales and dolphins to understand why they died. Most cases (62%) were linked to diseases, and about half of those animals were in poor body condition due to long-term illness.
Infectious agents proved to be a significant threat, affecting 11 different species, including striped dolphins and Longman's beaked whales. Two of the most concerning pathogens were morbillivirus and brucella, which can cause serious brain and lung problems in marine mammals.
Toxoplasmosis—a parasite that infects warm-blooded animals and spreads through cat feces across the environment—was responsible for the deaths of two spinner dolphins and one bottlenose dolphin.
The study revealed that 29% of all strandings were linked to anthropogenic (human-caused) trauma. Vessel strikes were a significant risk, resulting in fatal vertebral and skull fractures for seven individuals, including two pygmy sperm whales, two humpback whale calves, a goose-beaked whale, a spinner dolphin and a striped dolphin.
Interactions with marine debris and fisheries were confirmed as fatal in multiple cases, including a sperm whale that died from plastic and fishery debris blocking its stomach and a bottlenose dolphin that died after a fishhook tore into it.
Kristi West et al, Pacific Islands cetaceans: a review of strandings from 2006-2024, Diseases of Aquatic Organisms (2025). DOI: 10.3354/dao03877
Dec 23, 2025
Dr. Krishna Kumari Challa
Gut bacteria may play role in bipolar depression by directly influencing brain connectivity
Bipolar disorder (BD) is a psychiatric disorder characterized by extreme mood changes. Individuals diagnosed with BD typically alternate between periods of high energy, euphoria, irritability and/or impulsivity (i.e., manic episodes) and others marked by feelings of sadness, low energy, and hopelessness (i.e., depression).
While there are now several medications that can help patients to manage the disorder and stabilize their mood, many of these drugs have side effects and dosages often need to be periodically adjusted. Recent studies suggest that the bacteria and microorganisms living in the digestive system, also known as gut microbiota, play a key role in mental health and might also contribute to some symptoms of BD.
Researchers recently carried out a study investigating the possible connection between gut microbiota and the depressive episodes experienced by people diagnosed with BD. Their findings, published in Molecular Psychiatry, suggest that the microorganisms in the digestive system can directly influence connections between specific brain regions known to be affected by BD depression.
Adequate evidence has shown that gut microbial dysbiosis is an emerging disease phenotype of BD and is closely related to clinical symptoms of this intractable disease, wrote the researchers in their paper.
To explore the link between gut microbiota and BD depression, the researchers collected gut bacteria from individuals diagnosed with BD who were going through a depressive phase. They then transplanted these bacteria into the digestive system of healthy mice.
They found that bipolar depression-like mice presented with a decrease in the density of dendrite spines in medial prefrontal neurons, and translation post-synapse as a key contributor to the changes in synaptic plasticity.
In addition, analysis of synaptic connectivity in the mPFC revealed that compared to control mice, fewer connections were observed between ventral tegmental area and mPFC glutamate neurons and dopamine response was decreased in BD mice.
Notably, the researchers found that after they received the microbiota taken from individuals who were experiencing BD depression, the mice also started exhibiting depression-like behaviors. In addition, neurons in two brain regions known to be implicated in mood regulation, namely the ventral tegmental area (VTA) and the medial prefrontal cortex (mPFC), appeared to be less connected with each other.
The team also observed disruptions in the production of proteins and reduced dopamine signaling. Dopamine signaling (i.e., the release of dopamine) is essential for maintaining motivation and emotional regulation.
The results of this study confirm that microorganisms and bacteria in the gut can influence the connections between neurons in different brain regions. These altered connections could in turn have an impact on motivation, mood regulation and the processing of emotions.
Part1
Dec 24, 2025
Dr. Krishna Kumari Challa
The team's findings will need to be validated in humans before they can be reliably translated into psychiatric and medical insight. In the future, however, they could potentially help to identify promising pathways for the treatment of depression in patients diagnosed with BD, which are designed to alter their gut microbiota.
Anying Tang et al, Gut microbiota modulates synaptic plasticity, connectivity, and dopamine transmission in the VTA-mPFC pathway in bipolar depression, Molecular Psychiatry (2025). DOI: 10.1038/s41380-025-03398-y.
Part 2
Dec 24, 2025
Dr. Krishna Kumari Challa
Brain chemistry can reactivate or suppress dormant HIV
Human immunodeficiency virus (HIV) infections are still fairly common and an estimated 40 million people worldwide are currently living with this condition. The HIV virus attacks the body's immune system and thus makes those who contract it more vulnerable to a wide range of infections.
While there is still no known cure for HIV, there are now various treatment options that allow affected patients to live long and healthy lives. When treated with antiretroviral therapy (ART), the virus is known to remain in a latent state, essentially 'hiding' inside cells and forming a reservoir of dormant virus. If the medication is stopped, however, the virus can be re-awoken, causing severe immune deficiencies again.
Researchers have recently been investigating how the brain, particularly tiny molecules and protein-carrying packages released by cells, influence the persistence of HIV. In a new paper, published in Molecular Psychiatry, they presented new findings that shed new light on molecular mechanisms that can either re-ignite or suppress latent HIV.
In their experiments the researchers found that ECs collected from the brains of SIV-infected but untreated macaques strongly re-activated latent virus reservoirs increasing the activity of viral genes, the production of proteins and causing the virus to spread between cells. Interestingly, however, particles extracted from the brains of infected macaques who were treated with cannabinoids were found to suppress the re-activation of the virus.
"Cannabinoids have been shown to inhibit neuroinflammation," said the authors of the research paper. They showed that cannabinoids exert similar anti-inflammatory effects via EVs and in the current study on ECs, we report that ECs isolated from brains (basal ganglia) of rhesus monkeys have this anti-inflammatory effect and that cannabinoids modulate the cargos of the ECs, with resultant effects on latent HIV reservoirs.
Overall, the findings gathered by these researchers suggest that the brain's chemistry, particularly ECs, do play a key role in the reactivation or suppression of dormant HIV. In the future, their work could pave the way for the development of new drugs and therapeutic interventions aimed at better managing, or perhaps even curing, HIV infections.
Wasifa Naushad et al, Extracellular condensates (ECs) are endogenous modulators of HIV transcription and latency reactivation, Molecular Psychiatry (2025). DOI: 10.1038/s41380-025-03354-w.
Dec 24, 2025
Dr. Krishna Kumari Challa
The global fish trade is spreading 'forever chemicals' around the world
Eating fish may well be good for you, but it carries a hidden risk of exposure to so-called "forever chemicals." A new study published in the journal Science has revealed that the global seafood trade is acting as a massive delivery system for per- and polyfluoroalkyl substances (PFAS), industrial pollutants that persist in the environment for decades.
These forever chemicals are used in many products, from nonstick cookware and cosmetics to food packaging and firefighting foams. They are extremely resistant to breaking down in the environment and have been linked to a variety of serious illnesses such as cancer and liver disease.
PFAS can travel long distances around the planet in the air and through water. Once they wash into the ocean, they are absorbed by tiny organisms at the bottom of the food chain, such as plankton and algae. Because these chemicals do not break down, they accumulate in their bodies, and when small fish eat them, the toxic substances pass up the food chain. Large predatory fish, the kind that end up on our dinner plates, eat these smaller marine creatures, and as a result, the chemical concentrations build up in their tissues and organs.
In their paper, the researchers set out to map how these chemicals move once they are inside the fish. They built a computer model covering 212 different species to track how toxins accumulate up the food chain and then validated this with lab tests on fish from numerous countries. Then the team combined this data with global trade records to see how the fish and PFAS travel from one country to another.
One of the most significant findings was that the international fish trade acts like a global conveyor belt, redistributing PFAS from contaminated regions to consumers thousands of miles away.
Before this study, it was generally assumed that forever chemicals were a local problem. If your country's rivers and seas were clean, then so were the fish. However, a nation with clean water can still be exposed to high levels of PFAS through the seafood it imports from other parts of the world. For example, researchers found that Italians buy only 11% of their fish from Sweden, yet this accounts for more than 35% of their PFAS exposure.
Given that this problem doesn't respect borders, researchers argue that a unified global strategy is needed to protect public health.
Wenhui Qiu et al, Risks of per- and polyfluoroalkyl substance exposure through marine fish consumption, Science (2025). DOI: 10.1126/science.adr0351
Jennifer Sun et al, Reevaluating PFAS exposure risks from marine fish, Science (2025). DOI: 10.1126/science.aed7431
Dec 24, 2025
Dr. Krishna Kumari Challa
Raindrops form 'sandballs' as they roll downhill, contributing more to erosion than previously thought
We know that the initial splash of raindrops on soil contributes to erosion, but a new study, published in the Proceedings of the National Academy of Sciences, finds that the journey of the raindrop downhill might have an even bigger impact on erosion than the initial splash.
Researchers observed natural raindrops hitting the surface of a hillside and noticed that they collected particles of sand as they rolled downhill. This spurred the researchers to document the event with a camera and then take the idea to the lab.
In the lab, they constructed a 1.2 meter long bed covered with dry silicate sand and tilted at an angle of 30°. The lab conditions enabled the team to properly document the phenomenon by recording the evolution of the raindrops' shapes as they rolled and take precise measurements of the relevant parameters. They found that each raindrop formed what they refer to as "sandballs" and that they took on differing shapes, depending on the conditions, and that the sandballs can move up to 10 times more soil than the initial splash alone.
"In the initial rolling stage, drops rapidly increase their speed and sediment entrainment rate. Under increasing centrifugal force, the rolling drops undergo a metamorphosis: Their rounded shape destabilizes, as both liquid and entrained grains drift away from the core to create sandballs," the study authors write in their paper.
The researchers found that the sandy raindrops formed two distinct shapes: a peanut shape and a doughnut shape. Peanuts occurred at comparably lower velocities and maintained their grains at the surface of the drop. They only gather grains up to a certain point and then usually plateau.
"Once their mass plateaus, peanuts continue to increase their angular velocity as they roll; this sometimes causes a shift in their mode of motion, triggering an additional phase of mass accumulation. Other times, peanuts break, tumble slower or settle. If peanuts survive to the end of the slope and roll onto a flat surface, they immediately fall apart," the study authors explain.
Instead of only gathering grains at the surface, doughnut-shaped drops absorb sand grains into their interior volume, making them more dense and opaque in appearance. The researchers call the emergence of these kinds of drops "unexpected."
The team found that these drops destabilize into the doughnut shape from axisymmetric radial stretching. These shapes only occur at very high spin rates in pure-liquid drops, but occurred at slightly lower rates in the lab experiments due to the water-glycerol mixture used in the lab-based drops.
Part 1
Dec 24, 2025
Dr. Krishna Kumari Challa
The study authors write, "Fully developed doughnuts continue to speed up (above 1 m/s), until a point where they sometimes break apart in an apparent fracture process. This breakage occurs when the tensile force driven by the centrifugal sandball stretching overcomes the strength of capillary bonds, producing child sandballs that carve their own track as they tumble down the slope."
Studying the shapes that raindrops take on as they tumble down dry dirt hills might seem frivolous, but these dynamics have real implications for soil erosion models, which are used for predicting soil loss from rain. These models help with conservation planning, land management, and environmental assessment by estimating erosion rates, identifying more vulnerable areas, designing control measures and evaluating land health in agriculture.
Bertil Trottet et al, Sandball genesis from raindrops, Proceedings of the National Academy of Sciences (2025). DOI: 10.1073/pnas.2519392122
Part 2
Dec 24, 2025
Dr. Krishna Kumari Challa
New species are being discovered faster than ever before, study suggests
According to a new study published in Science Advances, scientists are discovering species quicker than ever before, with more than 16,000 new species discovered each year. The trend shows no sign of slowing, and the team behind the new paper predicts that the biodiversity among certain groups, such as plants, fungi, arachnids, fishes and amphibians is richer than scientists originally thought.
Researchers analyzed the taxonomic histories of roughly 2 million species, spanning all groups of living organisms. Between 2015 and 2020—the most recent period with comprehensive data—researchers documented an average of more than 16,000 new species each year, including more than 10,000 animals (dominated by arthropods and insects), 2,500 plants and 2,000 fungi.
and the good news is that this rate of new species discovery far outpaces the rate of species extinctions, which researchers calculated to about 10 per year.
These thousands of newly found species each year are not just microscopic organisms, but include insects, plants, fungi and even hundreds of new vertebrates.
The team also analyzed the rates of new species appearing over time to project how many species will be discovered and described in the future. For example, they projected that there might be as many as 115,000 fish species and 41,000 amphibian species, even though there are only about 42,000 fish and 9,000 amphibian species described now. They also projected that the final number of plant species might be over a half million.
Discovering new species is important because these species can't be protected until they're scientifically described.
Additionally, the discovery of new species contributes to finding new natural products for human benefit.
Spider and snake venoms and many plants and fungi also contain natural products with potential medicinal applications, including treatments for pain and cancer.
Beyond medicine, many species have adaptations that can inspire human inventions, such as materials mimicking the "super-clinging" feet that allow geckos to climb up vertical surfaces. Scientists are still just scratching the surface of what these species can do for humanity.
Xin Li et al, The past and future of known biodiversity: Rates, patterns, and projections of new species over time, Science Advances (2025). DOI: 10.1126/sciadv.adz3071
Dec 24, 2025
Dr. Krishna Kumari Challa
Fathers' microplastics exposure tied to their children's metabolic problems
Paternal exposure to microplastics in mice leads to metabolic dysfunction in offspring, with female progeny showing increased susceptibility to diabetes and altered gene expression linked to inflammation. These effects are associated with changes in sperm small noncoding RNAs, indicating a mechanism for transgenerational impact of environmental pollutants.
A new study has shown for the first time that a father's exposure to microplastics (MPs) can trigger metabolic dysfunctions in his offspring. The research, conducted using mouse models, highlights a previously unknown pathway through which environmental pollutants impact the health of future generations.
While MPs have already been detected in human reproductive systems, the study, published in the Journal of the Endocrine Society, is the first to bridge the gap between paternal exposure to MPs and the long-term health of the next generation (the "F1 offspring").
MPs are tiny plastic particles (less than 5 millimeters) resulting from the breakdown of consumer products and industrial waste. Metabolic disorders refer to a cluster of conditions—including increased blood pressure, high blood sugar, and excess body fat—that increase the risk of heart disease and diabetes.
Key findings and sex-specific effects The research team found that female offspring of male mice exposed to MPs were significantly more susceptible to metabolic disorders than offspring of unexposed fathers, despite all offspring being fed the same high-fat diet.
"The exact reasons for this sex-specific effect are still unclear", say the researchers. They observed upregulation of pro-inflammatory and pro-diabetic genes in their livers—genes previously linked to diabetes. These changes were not seen in male offspring.
The research team found that while male offspring did not develop diabetes, they showed a slight yet significant decrease in fat mass. Female offspring showed decreased muscle mass alongside increased diabetes.
Seung Hyun Park et al, Paternal microplastic exposure alters sperm small non-coding RNAs and affects offspring metabolic health in mice, Journal of the Endocrine Society (2025). DOI: 10.1210/jendso/bvaf214
Dec 24, 2025
Dr. Krishna Kumari Challa
Why mangoes fall before they're ripe—and how science is helping them hang on
Why your mango tree drops fruit before it's ripe? Each season, mango growers across the world watch helplessly as millions of mangoes fall to the ground too early.
These mangoes never ripen properly, never reach consumers, and represent a major loss—both economically and environmentally.
Premature fruit drop is a major contributor to low mango yields, with as little as 0.1% of fruits reaching maturity. This costs growers millions and wastes valuable resources.
As climate stress intensifies, understanding why fruit is lost before harvest has global significance. It affects everything from food security to farm profitability.
Its sensitivity to environmental stress makes it vulnerable in a less predictable and more extreme climate. Drought, heat waves, and even leaf loss can influence a natural process that leads to fruit drop.
Just like humans, plants rely on hormones to keep things growing and functioning smoothly.
These chemical messengers help regulate everything from flowering to fruit development.
But when plants experience stress, hormone levels shift. The plant starts reallocating resources to survive. Dropping fruit is often one of the first sacrifices.
One key resource that plants reallocate is carbohydrates. Developing fruit requires a steady supply of sugars, but under stress—such as leaf damage or water scarcity—the tree may struggle to produce or transport enough.
This can trigger fruit drop, as the plant prioritizes survival over reproduction.
Stress not only disrupts carbohydrate supply but also interferes with the hormonal balance in mango trees. This triggers what we call a molecular "quit signal": a message from the plant to let go of its fruit.
This signal is a part of a complex network of gene activity and hormonal cues that help the tree decide when to shed fruit.
Researchers are studying the molecular pathways behind this signal by analyzing gene signals from mango pedicel tissue—the stem that connects the fruit to the tree.
This tissue acts like a control center, managing the flow of nutrients and signals between the tree and the developing fruit. It's where the tree and fruit stay in touch, especially during stress.
By analyzing which genes are turned on or off, we can pinpoint the molecular signals involved in fruit drop, particularly those related to hormones.
This helps us move from just observing fruit drop to developing tools to control it.
One promising solution is the use of plant growth regulators, which are synthetic versions of plant hormones.
These can be applied to mango trees to help stabilize hormone levels during stressful conditions.
It's a bit like giving the tree a hormonal pep talk, encouraging it to hold onto fruit even when times are tough.
Applying plant growth regulators during flowering, before fruit has fully emerged, was more effective than applying them later in the season.
This early intervention helped reinforce the hormonal signals that support fruit retention. Initial trials have increased tree yield by up to 17%.
Even small-scale growers might one day use targeted treatments to help their trees hold on to fruit longer.
Part 1
Dec 25, 2025
Dr. Krishna Kumari Challa
For consumers, reducing fruit drop means better access to fresh, affordable produce. For growers, it's about staying viable in an increasingly unpredictable climate. And for policymakers, it's about preparing the horticultural industry for the challenges ahead.
Importantly, fruit drop isn't unique to mangoes. Apples, citrus, and avocados also suffer losses due to hormonal imbalances triggered by environmental stress.
Better understanding the molecular mechanisms controlling fruit drop in mango, could benefit a wide range of fruit crops globally as the climate changes.
This article is republished from THE CONVERSATION under a Creative Commons license. Read the original article.
Part 2
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Dec 25, 2025
Dr. Krishna Kumari Challa
Why do reindeer eyes change colour?
Dec 26, 2025