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Meta-analysis reveals functional diversity in microbial iron cycling across environments, highlighting temperature as a key filter.
Microbial iron redox cycling underpins key biogeochemical processes, yet the functional diversity, ecological roles, and trait architectures of iron-transforming microbes remain poorly synthesized across global environments. Here, we present a systematic review and trait-based meta-analysis of 387 microbial taxa spanning 314 studies and 76 years of research, integrating phenotypic, genomic, and environmental data to define ecologically coherent MIRC guilds. Rather than relying on taxonomy, our framework delineates first-order functional guilds - Fe(III)-reducers, Fe(II)-oxidizers, and dual-capacity Fe oxidizers/reducers - and resolves second-order guilds based on trait syndromes such as acidophily, redox flexibility, or metabolic breadth. Trait profiling revealed that iron-cycling capacities frequently transcend phylogenetic boundaries, with multiple guilds converging in chemically stratified hotspots like hot springs, hydrothermal vents, and acid mine drainages. Dual-capacity Fe oxidizers/reducers (e.g., Acidithiobacillus ferrooxidans , Metallosphaera sedula ) emerged as overlooked mediators of “cryptic” iron cycling, possessing genomic repertoires capable of toggling between oxidative and reductive modes in response to redox oscillations. Hierarchical clustering and kernel density analyses of ecophysiological traits highlighted niche partitioning along key environmental filters, including pH, iron availability, salinity, and temperature. Collectively, this work introduces the Guild Exploitation Pattern as a conceptual lens for understanding iron microbiome assembly, providing a data-driven foundation for predicting microbial contributions to iron cycling under changing environmental conditions.
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Díaz-González et al. (2025) studied this question.
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