Abstract
Abstract Fungi are key organisms in terrestrial ecosystems, functioning as decomposers, pathogens, and symbionts. Identifying the mechanisms that shape metacommunity patterns is likely to be critical for predicting how ecosystems will respond to global environmental change. Using fungal occurrence data and a hierarchical approach that combines three elements of metacommunity structure—coherence, turnover and boundary clumping—we identified the structures that best describe metacommunity patterns. We related these patterns to underlying environmental and spatial variables known to influence fungal distribution, and determined the relative importance of the environment and geographic distance in structuring fungal metacommunities. Fungal metacommunities had Clementsian and quasi-Clementsian structures, indicating that species distributions were compartmentalized along a dominant environmental gradient. This gradient was strongly associated with annual precipitation, precipitation seasonality and pH for the entire metacommunity. Variance partitioning revealed that the environment was relatively more important than geographic distance in explaining metacommunity patterns, indicating that niche-based processes are crucial in shaping species distributions among sites. However, the strength of the relationship between the latent gradient and environmental factors and the relative contributions of the environment and geographic distance to metacommunity structure varied across groups, suggesting that interactions among habitat, dispersal and life-history might be driving these differences.
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