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Evolutionary Biology

Defying Darwin: Scientists Discover Worms Rewrite Their DNA to Survive on Land

New research is shaking up our understanding of evolution by revealing that some species may not evolve gradually at all. Instead, scientists discovered that certain marine worms experienced an explosive genetic makeover when they transitioned to life on land over 200 million years ago. Their entire genome broke into pieces and was randomly reassembled an event so extreme it stunned researchers. This radical shift supports the theory of “punctuated equilibrium,” where species remain unchanged for ages and then suddenly leap forward.

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The article delves into the fascinating world of evolutionary biology, where scientists have made groundbreaking discoveries about the genetic mechanisms that allowed ancient marine worms to transition to life on land over 200 million years ago. This study, led by the Institute of Evolutionary Biology (IBE), challenges traditional views of evolution and reveals a more complex and dynamic process than previously thought.

The researchers sequenced the high-quality genomes of various earthworms and compared them to other closely related annelid species, such as leeches and bristle worms or polychaetes. Their analysis revealed an unexpected result: the annelids’ genomes were not transformed gradually, but in isolated explosions of deep genetic remodelling.

This phenomenon challenges the models of genome evolution known to date, given that many of the genomic structures observed in other species are almost perfectly conserved. The researchers discovered that marine worms broke their genome into a thousand pieces only to reconstruct it and continue their evolutionary path on land.

The study suggests that these adjustments not only moved genes around but also joined fragments that had been separated, creating new “genetic chimeras” which would have driven their evolution. This radical genetic mechanism could provide evolutionary responses to the challenges of adapting to life on land, such as breathing air or being exposed to sunlight.

The observations in the study are consistent with a punctuated equilibrium model, where we observe an explosion of genomic changes after a long period of stability. However, the lack of experimental data for or against makes it difficult to validate this theory.

This phenomenon has previously been observed in the progression of cancer in humans, and the term chromoanagenesis covers several mechanisms that break down and reorganize chromosomes in cancerous cells. The only difference is that while these genomic breakdowns and reorganizations are tolerated by worms, in humans they lead to diseases.

The study opens the door to a better understanding of the potency of this radical genomic mechanism, with implications for human health. It also reawakens one of the liveliest scientific debates of our time, as both visions – Darwin’s and Gould’s – are compatible and complementary.

In the future, a larger investigation of the genomic architecture of less-studied invertebrates could shed light on the genomic mechanisms shaping the evolution of species. There is a great diversity hidden in the invertebrates, and studying them could bring new discoveries about the diversity and plasticity of genomic organization and challenge dogmas on how we think genomes are organized.

The study involved the collaboration of research staff from various institutions, including the Universitat Autònoma de Barcelona, Trinity College, the Universidad Complutense de Madrid, the University of Köln, and the Université Libre de Bruxelles.

The study received support from SEA2LAND (Starting Grant funded by the European Research Council) and from the Catalan Biogenome Project, which funded the sequencing of one of the worm genomes.

Behavioral Science

“Rewired for Romance: Scientists Give Gift-Giving Behavior to Singing Fruit Flies”

By flipping a single genetic switch, researchers made one fruit fly species adopt the gift-giving courtship of another, showing how tiny brain rewiring can drive evolutionary change.

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Rewired for Romance: Scientists Give Gift-Giving Behavior to Singing Fruit Flies

In a groundbreaking study published in the journal Science, researchers from Japan have successfully transferred a unique courtship behavior from one species of fruit fly to another. By activating a single gene in insulin-producing neurons, the team made Drosophila melanogaster, a species that typically sings “courtship songs,” perform a gift-giving ritual it had never done before.

The study reveals that the reason for this difference lies in the connection between insulin-producing neurons and the courtship control center in the brain. In gift-giving flies (D. subobscura), these cells are connected, while in singing flies (D. melanogaster), they remain disconnected. This discovery highlights that the evolution of novel behaviors does not necessarily require the emergence of new neurons; instead, small-scale genetic rewiring can lead to behavioral diversification and species differentiation.

The researchers inserted DNA into D. subobscura embryos to create flies with heat-activated proteins in specific brain cells. They used heat to activate groups of these cells and compared the brains of flies that did and did not regurgitate food. The study identified 16-18 insulin-producing neurons that make the male-specific protein FruM, clustered in a part of the brain called the pars intercerebralis.

“Our findings indicate that the evolution of novel behaviors does not necessarily require the emergence of new neurons; instead, small-scale genetic rewiring in a few preexisting neurons can lead to behavioral diversification and, ultimately, contribute to species differentiation,” said Dr. Yusuke Hara, co-lead author from the National Institute of Information and Communications Technology (NICT).

This study demonstrates how scientists can trace complex behaviors like nuptial gift-giving back to their genetic roots to understand how evolution creates entirely new strategies that help species survive and reproduce.

The research was conducted with support from KAKENHI Grant-in-Aid for Scientific Research and has been published in the journal Science on August 14, 2025.

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Behavioral Science

The Amazing Ant Strategy That Can Revolutionize Robotics

Weaver ants have cracked a teamwork puzzle that humans have struggled with for over a century — instead of slacking off as their group grows, they work harder. These tiny architects not only build elaborate leaf nests but also double their pulling power when more ants join in. Using a “force ratchet” system where some pull while others anchor, they outperform the efficiency of human teams and could inspire revolutionary advances in robotics cooperation.

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The surprising strategy employed by weaver ants has left scientists stunned, as their unique approach to teamwork could potentially transform the field of robotics. A recent study published in Current Biology reveals that individual weaver ants actually increase their contribution to tasks when working in larger groups, defying the long-standing problem of declining performance with team size.

This phenomenon was first observed by French engineer Max Ringelmann in 1913, who found that human teams’ total force increased as more people joined in, but each individual’s contribution decreased. In contrast, weaver ants (Oecophylla smaragdina) have evolved to form super-efficient teams where individuals actually get better at working together as the group gets bigger.

Lead author Madelyne Stewardson from Macquarie University explains that each individual ant almost doubles their pulling force as team size increases. The researchers set up experiments enticing weaver ant colonies to form pulling chains to move an artificial leaf connected to a force meter. They found that the ants split their work into two jobs: some actively pull while others act like anchors to store the pulling force.

The key to this mechanism lies in the “force ratchet” theory developed by co-lead author Dr Daniele Carlesso from the University of Konstanz. Ants at the back of chains stretch out their bodies to resist and store the pulling force, while ants at the front keep actively pulling. This method allows longer chains of ants to have more grip on the ground, better resisting the force of the leaf pulling back.

The discovery has significant implications for robotics, as current robots only output the same force when working in teams as when alone. Dr Chris Reid from Macquarie’s School of Natural Sciences says that programming robots to adopt ant-inspired cooperative strategies could allow teams of autonomous robots to work together more efficiently.

This rewritten article maintains the core ideas but improves clarity, structure, and style, making it understandable to a general audience. The added prompt for image generation provides a visual representation of the weaver ant colony working together.

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Early Humans

The Hidden Legacy of the Denisovans: Uncovering the Secrets of Human Evolution

Denisovans, a mysterious human relative, left behind far more than a handful of fossils—they left genetic fingerprints in modern humans across the globe. Multiple interbreeding events with distinct Denisovan populations helped shape traits like high-altitude survival in Tibetans, cold-weather adaptation in Inuits, and enhanced immunity. Their influence spanned from Siberia to South America, and scientists are now uncovering how these genetic gifts transformed human evolution, even with such limited physical remains.

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The discovery of the Denisovans has revolutionized our understanding of human evolution. In 2010, scientists uncovered the first draft of the Neanderthal genome, confirming that early humans had interbred with these extinct relatives. Just months later, a finger bone found in Denisova Cave revealed the presence of another unknown hominin group, the Denisovans. Like their Neanderthal counterparts, researchers have found evidence of interbreeding between modern humans and Denisovans.

According to Dr. Linda Ongaro, Postdoctoral Researcher at Trinity College Dublin’s School of Genetics and Microbiology, this phenomenon is not unique to a single event but rather the result of multiple interbreeding episodes that shaped the course of human history. “It’s a common misconception that humans evolved suddenly and neatly from one common ancestor,” she notes. “The more we learn, the more we realize interbreeding with different hominins occurred and helped shape the people we are today.”

Despite the limited Denisovan fossil record, scientists have managed to uncover significant evidence of their genetic legacy. By leveraging surviving segments in modern human genomes, researchers have identified at least three past events where genes from distinct Denisovan populations were incorporated into the genetic signatures of humans.

These events reveal varying degrees of genetic similarity to the Denisovan remains found in the Altai region, suggesting a complex relationship among these closely related groups. In their review, Dr. Ongaro and Professor Emilia Huerta-Sanchez highlight evidence that Denisovans lived across a vast territory stretching from Siberia to Southeast Asia and from Oceania to South America. Different groups appear to have been adapted to their own specific environments.

Moreover, scientists have detailed several Denisovan-derived genes that provided survival advantages in different parts of the world. For example, one genetic locus confers tolerance to hypoxia (low oxygen conditions), which makes sense in Tibetan populations; multiple genes confer heightened immunity; and one gene impacts lipid metabolism, providing heat when stimulated by cold, giving an advantage to Inuit populations in the Arctic.

Dr. Ongaro emphasizes that there are numerous future directions for research that will help tell a more complete story of how the Denisovans impacted modern humans. These include more detailed genetic analyses in understudied populations and integrating more genetic data with archaeological information, which could reveal currently hidden traces of Denisovan ancestry.

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