ArticleeLife2024
Variation in thermal physiology can drive the temperature-dependence of microbial community richness.
Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- Ecological acclimation of microbial communities to rising temperatures: growth, respiration, and interactions.Applied and environmental microbiology · 2026Review
- General Predictions for the Effects of Warming on Competition.Ecology letters · 2026Article
- Continental-Scale Climatic Zones Drive Reorganization of Lake Sediment Microbiome: Diversity, Assembly and Interaction Networks.Microorganisms · 2026Article
- Accuracy of the Lotka-Volterra model fails in strongly coupled microbial consumer-resource systems.PLoS computational biology · 2025Article
- Climate-linked biogeography of mycorrhizal fungal spore traits.Proceedings of the National Academy of Sciences of the United States of America · 2025Article
- Cross-feeding creates tipping points in microbiome diversity.Proceedings of the National Academy of Sciences of the United States of America · 2025Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
Predicting how species diversity changes along environmental gradients is an enduring problem in ecology. In microbes, current theories tend to invoke energy availability and enzyme kinetics as the main drivers of temperature-richness relationships. Here, we derive a general empirically-grounded theory that can explain this phenomenon by linking microbial species richness in competitive communities to variation in the temperature-dependence of their interaction and growth rates. Specifically, the shape of the microbial community temperature-richness relationship depends on how rapidly the strength of effective competition between species pairs changes with temperature relative to the variance of their growth rates. Furthermore, it predicts that a thermal specialist-generalist tradeoff in growth rates alters coexistence by shifting this balance, causing richness to peak at relatively higher temperatures. Finally, we show that the observed patterns of variation in thermal performance curves of metabolic traits across extant bacterial taxa is indeed sufficient to generate the variety of community-level temperature-richness responses observed in the real world. Our results provide a new and general mechanism that can help explain temperature-diversity gradients in microbial communities, and provide a quantitative framework for interlinking variation in the thermal physiology of microbial species to their community-level diversity.
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Registered trials
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