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Biology subjects

Anderson, L. H.

Publications and source records attributed to Anderson, L. H..

2 recordsLinked to original sources

Geomorphic evolution of a Caribbean biological hotspot

Continental shelf archipelagos offer rare opportunities to test island biogeography in a time-resolved, non-equilibrium setting because postglacial sea-level rise drives datable changes in both island area and isolation. Yet most near-shore systems still lack reconstructions that integrate spatial changes in island configuration with duration-weighted histories of fragmentation. Such information is essential for interpreting modern genomic and biodiversity patterns and for evaluating responses to fragmentation such as extinction debt, immigration lag and adaptive responses over time. Here we reconstruct the land-sea geomorphic history of the Bocas del Toro Archipelago, Panama, combining high-resolution bathymetry and topography with a sea-level model corrected for sedimentation and tectonic movement. From this, we quantify multi-scale isolation, historical fragmentation dynamics, and composite metrics that integrate space and time. We show that present-day islands became isolated sequentially from 9.5 to 2.9 ka, with post-isolation area contraction rates varying 20-fold among islands. Over the same interval, shallow marine habitat (0-10 m depth) expanded ninefold as shelf flooding created space for reefs, seagrass, and mangroves. Extending the analyses through the Pleistocene reveals the modern archipelago is atypical and for much of the last million years, the region existed as continuous coastal lowland rather than discrete islands. Projections under moderate emissions scenarios predict [~]5% terrestrial habitat loss but [~]50% expansion of shallow marine habitat by 2150, though whether degraded Caribbean reefs can exploit this expansion remains uncertain. Exploratory correlations between species richness of terrestrial vertebrate groups and geomorphometric predictors reveal that island area, maximum elevation, and cumulative habitat availability since isolation are the strongest correlates of diversity, whilst buffer-zone isolation indices are confounded by covariation between island size and surrounding landmass in this continental shelf context. Overall, Bocas del Toro provides a time-calibrated natural experiment for testing how dynamic connectivity and isolation shaped island and coastal biodiversity.

evolutionary biology↗

Cooperativity and Avidity in Membrane Binding by C2AB Tandem Domains of Synaptotagmins 1 and 7

Synaptotagmin-1 (Syt-1) and synaptotagmin-7 (Syt-7) contain analogous tandem C2 domains, C2A and C2B, which together serve as a Ca2+ sensor to bind membranes and promote the stabilization of exocytotic fusion pores. Functionally, Syt-1 triggers fast release of neurotransmitters, while Syt-7 is involved in lower-Ca2+ processes such as hormone secretion. Evidence suggests that Syt-1 C2 domains bind membranes cooperatively, penetrating farther into membranes as the C2AB tandem than as individual C2 domains. In contrast, we previously reported that the two C2 domains of Syt-7 bind membranes independently, based in part on measurements of their liposome dissociation kinetics. Here, we have investigated the effects of C2A-C2B interdomain cooperativity with Syt-1 and Syt-7 using directly comparable measurements. We report Ca2+ sensitivities, dissociation kinetics, and membrane insertion using liposomes approximating physiological lipid compositions. Equilibrium Ca2+ titrations confirm that the Syt-7 C2AB tandem has a greater Ca2+ sensitivity of membrane binding than either of its individual domains. Stopped-flow fluorescence kinetic measurements show that Syt-1 C2AB dissociates from liposome membranes much more slowly than either of its isolated C2 domains, suggesting that the two C2 domains of Syt-1 bind membranes cooperatively. In contrast, the dominant population of Syt-7 C2AB has a dissociation rate comparable to its C2A domain, indicating a lack of cooperativity, while only a small subpopulation dissociates at a slower rate. Measurements using an environment-sensitive fluorescent probe indicate that the Syt-7 C2B domain inserts more deeply into membranes as part of the C2AB tandem, similarly to Syt-1. Overall, these measurements are consistent with a model in which the structural linkage of C2A and C2B impacts the membrane-binding geometry of synaptotagmin C2B domains, but imparts little or no cooperativity to Syt-7 membrane binding and dissociation events that are dominated by its C2A domain.

biophysics↗