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New research on the inner ear morphology of Neanderthals and their ancestors challenges the widely accepted theory that Neanderthals originated after an evolutionary event that implied the loss of part of their genetic diversity. The findings, based on fossil samples from Atapuerca (Spain) and Krapina (Croatia), as well as from various European and Western Asian sites have been published in Nature Communications.

Neanderthals emerged about 250,000 years ago from European populations—referred to as “pre-Neanderthals”—that inhabited the Eurasian continent between 500,000 and 250,000 years ago. It was long believed that no significant changes occurred throughout the evolution of Neanderthals, yet recent paleogenetic research based on DNA samples extracted from fossils revealed the existence of a drastic genetic diversity loss event between early Neanderthals (or ancient Neanderthals) and later ones (also referred to as “classic” Neanderthals).

Technically known as a “bottleneck,” this genetic loss is frequently the consequence of a reduction in the number of individuals in a population. Paleogenetic data indicate that the decline in took place approximately 110,000 years ago.

A new study by researchers at the Max Planck Institute for Evolutionary Biology (MPI-EB) sheds fresh light on one of the most debated concepts in biology: evolvability. The work provides the first experimental evidence showing how natural selection can shape genetic systems to enhance future capacity for evolution, challenging traditional perspectives on evolutionary processes.

The research is published in the journal Science. A related Perspective article also appears in Science.

The ability of organisms to generate adaptive genetic variation is crucial for evolutionary success, particularly in changing environments. The MPI-EB study investigates whether operates not merely as a “blind” process driven by but could actively favor mechanisms that channel mutations toward adaptive outcomes.

Humanity can farm more food from the seas to help feed the planet while shrinking mariculture’s negative impacts on biodiversity, according to new research led by the University of Michigan.

There is a catch, though: We need to be strategic about it.

The findings are published in the journal Nature Ecology & Evolution.

Isolated by mountains along the East African Rift is Lake Tanganyika. More than 400 miles long, it is the continent’s deepest lake and accounts for 16% of the world’s available freshwater. Between 2 and 3 million years ago, the number of virus species infecting fish in that immense lake exploded, and in a new study, UC Santa Cruz researchers propose that this explosion was perhaps triggered by the explosion of a distant star.

The new paper published in The Astrophysical Journal Letters, led by recent undergraduate student Caitlyn Nojiri and co-authored by astronomy and astrophysics professor Enrico Ramirez-Ruiz and postdoctoral fellow Noémie Globus, examined iron isotopes to identify a 2.5 million-year-old supernova.

The researchers connected this stellar explosion to a surge of radiation that pummeled Earth around the same time, and they assert that the blast was powerful enough to break the DNA of living creatures—possibly driving those viruses in Lake Tanganyika to mutate into new species.

For the study, the researchers used NASA’s powerful James Webb Space Telescope to observe Sagittarius A* to better understand its activity. After conducting several observations between 2023 and 2024, the researchers found that Sagittarius A* exhibited near-endless flare activity, ranging from faint flashes lasting a few seconds to massive eruptions occurring every day. Since Sagittarius A* interacts with the massive disk of gas and dust that comprises our galaxy, these results could help researchers better understand the formation and evolution of supermassive black holes throughout the universe.

“Flares are expected to happen in essentially all supermassive black holes, but our black hole is unique,” said Dr. Farhad Yusef-Zadeh, who is a professor at northwestern University and lead author of the study. “It is always bubbling with activity and never seems to reach a steady state. We observed the black hole multiple times throughout 2023 and 2024, and we noticed changes in every observation. We saw something different each time, which is really remarkable. Nothing ever stayed the same.”

A new study examines how complex chemical mixtures evolve under changing environmental conditions, offering insights into the prebiotic processes that may have led to life. Researchers exposed organic molecules to repeated wet-dry cycles and observed continuous transformations, selective organization, and synchronized population dynamics.

The findings indicate that environmental conditions played a crucial role in fostering the molecular complexity necessary for life’s emergence. By simulating early Earth’s conditions, the team found that instead of reacting randomly, molecules self-organized, evolved over time, and followed predictable patterns.

This challenges the notion that early chemical evolution was purely chaotic. Instead, the study suggests that natural environmental fluctuations guided the formation of increasingly complex molecules, ultimately contributing to the development of life’s fundamental building blocks.

“What we found was surprising: a jet stream rotates material around the planet’s equator, while a separate flow at lower levels of the atmosphere moves gas from the hot side to the cooler side,” said Dr. Julia Victoria Seidel.


What can a 3D map of an exoplanet’s atmosphere teach scientists about its weather patterns? This is what a recent study published in Nature hopes to address as an international team of researchers successfully produced the first 3D map of an exoplanet’s atmosphere, which is a groundbreaking achievement and will help scientists gain new insights into the formation and evolution of exoplanet atmospheres throughout the cosmos.

For the study, the researchers used the European Southern Observatory’s Very Large Telescope (ESO’s VLT) to observe WASP-121b, nicknamed Tylos, which is designated as an ultra-hot Jupiter that orbits its parent star in only 1.3 days (30 hours) and is located approximately 880 light-years from Earth. Due to its extremely close orbit, Tylos is tidally locked to its parent star, meaning one side is always facing it, resulting in searing temperatures on the sunlit side and incredibly cold temperatures on the far side.

In the end, the researchers successfully produced a 3D map of Tylos’ atmosphere, revealing weather patterns that include high-velocity winds carrying titanium and iron around the exoplanet, which becomes even more turbulent as the winds cross from the far side to the day side of Tylos. Additionally, this also marks the first time astronomers have produced a 3D map of an exoplanet’s atmosphere.

Two studies published in the latest issue of Science have revealed that birds, reptiles, and mammals have developed complex brain circuits independently, despite sharing a common ancestor. These findings challenge the traditional view of brain evolution and demonstrate that, while comparable brain functions exist among these groups, embryonic formation mechanisms and cell types have followed divergent evolutionary trajectories.

The pallium is the region where the neocortex forms in mammals, the part responsible for cognitive and complex functions that most distinguishes humans from other species. The pallium has traditionally been considered a comparable structure among mammals, birds, and reptiles, varying only in complexity levels. It was assumed that this region housed similar neuronal types, with equivalent circuits for sensory and cognitive processing.

Previous studies had identified the presence of shared excitatory and , as well as general connectivity patterns suggesting a similar evolutionary path in these vertebrate species.

While most animals reproduce sexually, some species rely solely on females for parthenogenetic reproduction. Even in these species, rare males occasionally appear. Whether these males retain reproductive functions is a key question in understanding the evolution of reproductive strategies.

A new study published in Ecology by a research team led by Assistant Professor Tomonari Nozaki from the National Institute for Basic Biology, Professor Kenji Suetsugu from Kobe University, and Associate Professor Shingo Kaneko from Fukushima University provides insight into this question. The researchers focused on the rare males of Ramulus mikado, a stick insect species in Japan, where parthenogenesis is predominant. Their analysis of male reproductive behavior reveals new findings.