Mapping mercury contamination in penguins of the Southern Ocean
Peer-Reviewed Publication
Updates every hour. Last Updated: 5-May-2025 07:09 ET (5-May-2025 11:09 GMT/UTC)
In 1962, when environmentalist and author Rachel Carson penned "Silent Spring," alerting the world to the dangers of the pesticide DDT, it was the reproductive threat to birds – the bald eagle in particular – that spurred people to action.
Six decades later, Rutgers University–New Brunswick researchers are taking the measure of another global environmental pollutant by drawing parallels to the crisis Carson identified. This time, the pollutant is mercury, and the sentinels are penguins living in the farthest reaches of the Antarctic Peninsula.
“With mercury, there’s an analogy to DDT,” said John Reinfelder, a professor in the Department of Environmental Sciences at the Rutgers School of Environmental and Biological Sciences, and co-author of a study published in Science of the Total Environment examining mercury levels in the flightless, aquatic birds.
Comprehensive reference genomes have now been assembled for six ape species: siamang (a Southeast Asian gibbon), Sumatran orangutan, Bornean orangutan, gorilla, bonobo and chimpanzee. Areas of their genomes previously inaccessible because of structural complexity have now mostly been resolved. The resource is already lending itself to comparative studies that offer new insights into human and ape evolution, and into what underlies the functional differences among these species.
Utilizing numerical simulations, researchers have succeeded in recreating the fluid dynamics of flowing cells like blood or immune cells in the circulatory system. The team recreated the cells by programing them as deformable ‘capsules’ and placed them in a tube with a pulsating ‘flow.’ This in-silico model revealed that capsules will move to a specific position depending on two factors: the deformation of the capsule and the pulsation frequency.
Researchers from Nanjing Medical University have developed a novel method to generate transient totipotent blastomere-like stem cells (tTBLCs) by treating mouse embryonic stem cells (mESCs) with a short-term high-dose of the splicing inhibitor Pladienolide B (PlaB). These tTBLCs can self-organize into blastocyst-like structures (blastoids) and recapitulate key pre-implantation developmental processes, offering a new tool for studying early embryogenesis and potential applications in drug screening.