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Elizabeth T. Borer

Publications and source records attributed to Elizabeth T. Borer.

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Anthropogenic disturbance expands the climatic limits of annual plant dominance

Disturbance regimes and nutrient inputs are changing worldwide, with consequences for the structure and functioning of plant communities. Classical life-history theory predicts that disturbance should shift communities from long-lived perennials toward short-lived annuals, and that nutrient enrichment may amplify this shift. However, these predictions have not been tested experimentally across broad environmental gradients. Here, using a global coordinated grassland experiment spanning 37 sites, we tested how physical disturbance, vegetation removal and shallow soil tillage, and fertilisation reshape annual-perennial balance, and whether disturbance relaxes the climatic limits of annual dominance. Disturbance nearly doubled the proportion of annual species and more than doubled the relative cover of annuals, whereas fertilisation had little influence and did not interact with disturbance. The disturbance-driven shift arose through contrasting pathways: in graminoids and legumes, it reflected the loss of perennial cover, while in forbs, the expansion of annual cover. In the absence of disturbance, annual dominance was restricted to systems with extremely hot and dry summers, but disturbance nearly tripled the extent of climate space in which annuals dominated. By rapidly reassembling after disturbance, annuals may help maintain vegetation cover, but their expansion also signals loss of perennial cover and the long-term ecosystem functions associated with it.

q-bio.OT

MIMIX: a Bayesian Mixed-Effects Model for Microbiome Data from Designed Experiments

Recent advances in bioinformatics have made high-throughput microbiome data widely available, and new statistical tools are required to maximize the information gained from these data. For example, analysis of high-dimensional microbiome data from designed experiments remains an open area in microbiome research. Contemporary analyses work on metrics that summarize collective properties of the microbiome, but such reductions preclude inference on the fine-scale effects of environmental stimuli on individual microbial taxa. Other approaches model the proportions or counts of individual taxa as response variables in mixed models, but these methods fail to account for complex correlation patterns among microbial communities. In this paper, we propose a novel Bayesian mixed-effects model that exploits cross-taxa correlations within the microbiome, a model we call MIMIX (MIcrobiome MIXed model). MIMIX offers global tests for treatment effects, local tests and estimation of treatment effects on individual taxa, quantification of the relative contribution from heterogeneous sources to microbiome variability, and identification of latent ecological subcommunities in the microbiome. MIMIX is tailored to large microbiome experiments using a combination of Bayesian factor analysis to efficiently represent dependence between taxa and Bayesian variable selection methods to achieve sparsity. We demonstrate the model using a simulation experiment and on a 2x2 factorial experiment of the effects of nutrient supplement and herbivore exclusion on the foliar fungal microbiome of $\textit{Andropogon gerardii}$, a perennial bunchgrass, as part of the global Nutrient Network research initiative.

stat.ME