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Biology subjects

Garcia, M. B.

Publications and source records attributed to Garcia, M. B..

3 recordsLinked to original sources

A demographic framework for assessing population vulnerability to contrasting perturbation regimes

Environmental change affects demographic rates through perturbations that differ in magnitude, duration, and frequency, yet their consequences for population vulnerability, i.e., potential population reduction, remain only partly understood. Here, we develop a general demographic framework that unifies pulse and press perturbations to better understand how life-history strategy shapes population declines across the fast-slow continuum. Using matrix population models for 12 plant and animal species with diverse generation time and life history strategies, we simulated perturbations acting independently on adult survival, juvenile survival, and fecundity, and measured their demographic consequences over comparable life-history timescales. We then integrated impacts across perturbation regimes to derive a novel comparative vulnerability metric and related this metric to species life-history descriptors. Across taxa, perturbations to adult survival consistently produced the strongest demographic impacts, with vulnerability increasing markedly towards slower life histories. Juvenile survival emerged as the main axis of demographic differentiation among species, whereas the effects of perturbations on fecundity were weaker and comparatively homogeneous across the continuum. Generation time strongly predicted vulnerability to survival perturbations, but not to reproductive output. Consistent with previous theoretical and empirical work, our results show that vulnerability is not a fixed species property, but an emergent outcome of the interaction between the perturbed vital rate, the temporal structure of environmental forcing, and the underlying life-history strategy. Importantly, as the vulnerability metric can be compared both across populations under a given perturbation regime and within populations across perturbation types and demographic targets, the framework also provides a basis for stage-specific and regime-specific management.

ecology↗

Rare plants can make an important contribution to sustain local biodiversity through biological interactions

Plants, as structural elements of habitats, contribute greatly to the maintenance of local biodiversity through their biological interactions. In this study we explore whether their rarity, according to Rabinowitzs (1981) three criteria, is related to the richness and diversity of arthropods and other plants they are associated to, in a gypsum-rich steppe. We first analysed whether the geographic abundance and ecological specialisation of 32 characteristic and dominant plant species are related to the diversity (richness and phylogenetic diversity (MPD)) and degree of local specialisation of arthropods associated with them (1,694 taxa). Then, we focused on a non endemic and non specialized plant in the study area (Krascheninnikovia ceratoides) to explore the effect of population size on two types of interactions: aerial arthropods and plant facilitation. Results indicate that: 1) plant species abundance (geographical range) is not related to the richness or MPD of communities of associated arthropods, 2) plant species ecological specialization (edaphic endemisms or gypsophiles) do not contribute differentially to the maintenance of singular arthropod communities, and 3) the community of aerial arthropods and plants interacting with K. ceratoides in a small population are not necessarily less diverse than those in patches of similar size in a large population. Results also revealed that the two plant species with fewer interactions (one rare, one widespread) do show the highest singularity in their interactions with arthropods. Our study illustrates the important contribution of rare plants to the conservation of local biodiversity.

ecology↗

Multimodal Spatial Proteomic Profiling in Acute Myeloid Leukemia

Acute myeloid leukemia (AML) resides in an immune rich microenvironment, yet, immune-based therapies have faltered in eliciting durable responses. Bridging this paradox requires a comprehensive understanding of leukemic interactions within the bone marrow microenvironment. We optimized a high-throughput tissue-microarray based pipeline for high-plex spatial immunofluorescence and mass cytometry imaging on a single slide, capturing immune, tumor, and structural components. Using unbiased clustering on the spatial K function, we unveiled the presence of tertiary lymphoid-like aggregates in bone marrow which we validated using spatial transcriptomics and an independent proteomics approach. We then found validated TLS signatures predictive of outcomes in AML using an integrated public 480 patient transcriptomic dataset. By harnessing high-plex spatial proteomics, we open the possibility of discovering of novel structures and interactions that underpin leukemic immune response. Further, our studys methodologies and resources can be adapted for other bone marrow diseases where decalcification and autofluorescence present challenges.

cancer biology↗