Early testing could make risky falls a thing of the past for elderly people
Peer-Reviewed Publication
Updates every hour. Last Updated: 23-Jul-2025 08:12 ET (23-Jul-2025 12:12 GMT/UTC)
What if the human body contained a natural bioreactor capable of regenerating vital organs? A collaborative team from Wenzhou Medical University, Nanjing University, and University of Macau has redefined the spleen’s potential, transforming it into a self-sustaining hub for organ regeneration, as published in Science Translational Medicine (May 21). This breakthrough could revolutionize treatments for type 1 diabetes and beyond.
22 May 2025/Kiel. Every year, total allowable catches (TACs) and fishing quotas are set across Europe through a multi-step process – and yet many fish stocks in EU waters remain overfished. A new analysis published today in the journal Science by researchers of the GEOMAR Helmholtz Centre for Ocean Research Kiel and Kiel University reveals that politically agreed-upon catch limits are not sustainable because fish stock sizes are systematically overestimated and quotas regularly exceed scientific advice. In order to promote profitable and sustainable fisheries, the researchers propose establishing an independent institution to determine ecosystem-based catch limits that management bodies must not exceed.
Ancient sloths ranged in size from tiny climbers to ground-dwelling giants. Now, researchers report this body size diversity was largely shaped by sloths’ habitats, and that these animals’ precipitous decline was likely a result of increasing human pressures, which also triggered the extinction of the large-bodied ground-dwelling animals. Today’s small arboreal sloths are the last remnants of a once-diverse group, surviving likely because they inhabited secluded forest canopies and avoided direct human pressures, say the authors. While only two small, tree-dwelling genera survive today – confined largely to the tropical rainforests of South and Central America – sloths (Folivora) represent a once-diverse, abundant, and widespread lineage of American mammals. During the late Cenozoic, more than 100 genera of sloths occupied a wide range of sizes and habitats, living across the Americas. Some terrestrial sloth species stood upwards of six meters tall and weighed several tons. However, by the end of the Pleistocene, the majority of these animals became extinct.
Alberto Boscaini and colleagues investigated the drivers behind the expansion and decline of body size variation in sloths over the past 35 million years, culminating in the eventual rapid collapse of the group. By combining fossil measurements, DNA and protein sequences, and advanced evolutionary modeling, Boscaini et al. reconstructed sloth evolutionary history across 67 genera and tested whether evolutionary changes in size were linked to habitat, diet, climate, predation, or other ecological pressures. The findings show that habitat preference – whether sloths lived in trees or on the ground – was the dominant factor shaping their body size evolution. Early sloths were large, ground-dwelling grazers. But transitions to tree-dwelling forms with smaller body sizes occurred multiple times, especially as open landscapes expanded. Gigantism evolved independently in several lineages, reflecting adaptive responses to cooling climates and ecological pressures. Yet, despite thriving for tens of millions of years, with body size diversity peaking in the Pleistocene, sloths experienced a sudden and dramatic decline beginning around 15,000 years ago. These declines do not align with the climatic changes of the time, but instead with the arrival of humans in the Americas. According to Boscaini et al., evidence suggests that human hunting drove the extinction of large-bodied terrestrial sloths.
For reporters interested in trends, a March 2019 Science Advances study by Gustavo Politis et al. highlights direct archaeological evidence of human giant sloth hunting and butchering in the Argentinian Pampas roughly 12,000 years ago. (https://www.science.org/doi/10.1126/sciadv.aau4546)
Most relapsing fever bacteria that infect humans are spread by ticks, but Borrelia recurrentis is unique in being transmitted between humans via body lice. Now, new genomic evidence from ancient British remains suggests that B. recurrentis diverged from its tick-borne relatives and began adapting to transmission by lice between 6000 and 4000 years ago – coinciding with the widespread use of wool textiles by humans. The findings underscore how ancient DNA can illuminate the origins and evolution of infectious diseases and how pathogens like B. recurrentis have been shaped by human social transformations. Several pathogenic bacterial species that once relied on ticks for transmission have independently evolved to use lice as vectors instead, including B. recurrentis. B. recurrentis has no known animal reservoir. Moreover, this louse-adapted pathogen tends to show higher virulence compared to its tick-borne relatives, suggesting a process of specialization. However, the precise timeline and genetic mechanisms behind its adaptation to lice and its increased virulence in humans remain uncertain.
Using advanced ancient DNA techniques optimized for degraded genetic material, Pooja Swali and colleagues recovered and analyzed four ancient B. recurrentis genomes from human remains in Britain, dating from roughly 2300 to 600 years ago. Through phylogenetic and pan-genome analysis, Swali et al. estimate that B. recurrentis diverged from its closest relative, B. duttonii, approximately 4700 – 5600 years ago. This period coincided with shifts in human behavior during the Neolithic-Bronze Age transition, such as the rise of sedentary lifestyles, the advent of wool textiles, and densely populated settlements. According to the authors, these changes may have facilitated the adaptation of B. recurrentis to the human body louse and also promoted genome reduction and host specialization. Over time, B. recurrentis underwent substantial genome reductions, particularly in plasmid-encoded genes. These genetic changes were accompanied by gains and losses of surface proteins that help the bacterium evade the host immune system.