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Biology subjects

Eichhorn, M.

Publications and source records attributed to Eichhorn, M..

2 recordsLinked to original sources

Impact of Fragmentation on the Metapopulation Structure of wild olive

Habitat fragmentation disrupts metapopulation dynamics by altering environmental conditions and constraining demographic processes critical for persistence and recruitment. In the dry Afromontane forests of northern Ethiopia, we investigated how natural and anthropogenic drivers affect seedlings, saplings, and mature tree dynamics of Olea europaea subsp. cuspidata across 34 patches. We used dynamic occurrence models to quantify effects of patch area, altitude, browsing, and disturbance. Our results indicate that high disturbance reduces seedling occurrence probability lower disturbance sites has seedling in 30% of survey plots, high disturbance would bring this down to 10% (median = -1.322, 95% CI: -2.703 to -0.283). Disturbance makes seedling less likely to persist, while large patch size help seedling persists (median = -0.93, 9 5 % CrI -1.87 - -0.02). For mature individuals, disturbance was the only significant predictor of occurrence probability, suggesting greater resistance to environmental and spatial variability compared to earlier life stages. These findings emphasize that while mature trees display resilience, the successful regeneration of Olea europaea is constrained by disturbance, but current level of browsing is not a threat. Management strategies for conservation should prioritise reducing disturbance through community engagement and forest stewardship to enhance regeneration potential and ensure long-term population viability.

ecology↗

Actomyosin, vimentin and LINC complex pull on osteosarcoma nuclei to deform on micropillar topography

Cell deformation occurs in many critical biological processes, including cell extravasation during immune response and cancer metastasis. These cells deform the nucleus, its largest and stiffest organelle, while passing through narrow constrictions in vivo and the underlying mechanisms still remain elusive. It is unclear which biochemical actors are responsible and whether the nucleus is pushed or pulled (or both) during deformation. Herein we use an easily-tunable poly-L-lactic acid micropillar topography, mimicking in vivo constrictions to determine the mechanisms responsible for nucleus deformation. Using biochemical tools, we determine that actomyosin contractility, vimentin and nucleo-cytoskeletal connections play essential roles in nuclear deformation, but not A-type lamins. We chemically tune the adhesiveness of the micropillars to show that pulling forces are predominantly responsible for the deformation of the nucleus. We confirm these results using an in silico cell model and propose a comprehensive mechanism for cellular and nuclear deformation during confinement. These results indicate that microstructured biomaterials are extremely versatile tools to understand how forces are exerted in biological systems and can be useful to dissect and mimic complex in vivo behaviour.

cell biology↗