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Biology subjects

Gelber, S.

Publications and source records attributed to Gelber, S..

2 recordsLinked to original sources

Geometric and demographic effects explain contrasting fragmentation-biodiversity relationships across scales

There is consensus that habitat loss is a major driver of biodiversity loss, while the effects of fragmentation, given a constant total habitat amount, are still debated. Here, we use a process-based metacommunity model to show how strongly scale- and context-dependent fragmentation-biodiversity relationships can emerge from the interplay of two types of fragmentation effects - geometric and demographic. Geometric effects arise from the spatial distribution of species and landscape modification, whereas demographic effects reflect long-term changes in species demographic rates following landscape modification. We introduce a novel approach to partitioning these two types of effects and assess how key ecological processes and factors, such as dispersal, habitat heterogeneity, and edge effects, influence geometric, demographic, and net fragmentation effects across spatial scales. We conclude that the framework of geometric and demographic effects can reconcile previous apparently conflicting results and hopefully unlock and advance the debate on biodiversity change in modified landscapes.

ecology↗

Discovery of a multipotent cell type from the term human placenta

We identify a population of multipotent CDX2 cells from term human placentas with clonal expansion, migratory capacity, and immune-privileged transcriptional profiles. Isolated from 180 healthy pregnancies, these cells differentiate into cardiomyocyte and vascular lineages in vitro and in vivo. Single-cell RNA sequencing uncovers distinct cardiogenic and vasculogenic subpopulations, along with immune-modulatory and chemotactic programs, providing a blueprint for precision-guided cardiovascular cell therapy. In a NOD/SCID myocardial infarction model, CDX2 cells restore cardiac function, and clonal propagation preserves their cardiovascular differentiation potential. These findings position placental CDX2 cells as an ethically accessible, regenerative platform for targeted treatment of cardiovascular disease.

cell biology↗