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Abstract Following disturbances such as wildfires, oak seedlings must form a symbiotic association with mycorrhizal fungi to survive. Wildfires, however, reduce available mycorrhizal fungal propagules in the soil. Ectomycorrhizal (ECM) fungi on oak seedlings sampled in severely burned (7 sites), moderately burned (7 sites), and unburned areas (8 sites) in the Great Smoky Mountains National Park were evaluated 21 months after the 2016 Chimney Tops 2 Wildfire by Sanger sequencing of the nuclear ribosomal DNA internal transcribed spacer region (nrITS; fungal barcode). Sequences were aligned and grouped into Operational Taxonomic Units (OTUs) based on well-supported phylogenetic clades and 98–100% nrITS sequence homology with sequences in GenBank. One hundred seventy-nine root-associated fungi comprising 124 OTUs were recovered after removing duplicates (the same fungus on two or more roots of the same plant). The ECM genusRussulawas the most diverse genus (25 OTUs), followed by theThelephora/Tomentellaclade (18 OTUs),Lactifluus(8 OTUs),Lactarius(4 OTUs), and Laccariaaff.laccata(2 OTUs).RussulaOTUs were identified more frequently on oak roots from burned areas and in burned soils, suggesting that someRussulataxa may have a selective advantage in burned areas. High alpha diversity occurred within each of the burn categories, but little overlap of taxa occurred between burn categories (high beta diversity). Approximately half of the recovered OTUs (100/179 total root-associated fungi = 55.9%) were found on a single plant. Oak seedlings growing in moderately and severely burned areas 21 months after a fire were capable of forming root associations with available fungi. In contrast to the expectation that root-associated fungal diversity would be reduced after a wildfire, diversity 1 year after the Chimney Tops 2 Fire was high with ectomycorrhizalLaccaria,Russulaceae, andThelephoraceaedominating. This study suggests that the availability of ECM fungi post-fire is not a barrier to oak re-establishment. 

ABSTRACT Disruptions to functionally important symbionts with global change will negatively impact plant fitness, with broader consequences for species' abundances, distribution, and community composition. Fungal endophytes that live inside plant leaves and roots could potentially mitigate plant heat stress from global warming. Conversely, disruptions of these symbioses could exacerbate the negative impacts of warming. To better understand the consistency and strength of warming‐induced changes to fungal endophytes, we examined fungal leaf and root endophytes in three grassland warming experiments in the US ranging from 2 to 25 years and spanning 2000 km, 12°C of mean annual temperature, and 600 mm of precipitation. We found that experimental warming disrupted symbiosis between plants and fungal endophytes. Colonization of plant tissues by septate fungi decreased in response to warming by 90% in plant leaves and 35% in roots. Warming also reduced fungal diversity and changed community composition in plant leaves, but not roots. The strength, but not direction, of warming effects on fungal endophytes varied by up to 75% among warming experiments. Finally, warming decoupled fungal endophytes from host metabolism by decreasing the correlation between endophyte community and host metabolome dissimilarity. These effects were strongest in the shorter‐term experiment, suggesting endophyte‐host metabolome function may acclimate to warming over decades. Overall, warming‐driven disruption of fungal endophyte community structure and function suggests that this symbiosis may not be a reliable mechanism to promote plant resilience and ameliorate stress responses under global change. 

Abstract Efforts to catalog global biodiversity have often focused on aboveground taxonomic diversity, with limited consideration of belowground communities. However, diversity aboveground may influence the diversity of belowground communities and vice versa. In addition to taxonomic diversity, the structural diversity of plant communities may be related to the diversity of soil bacterial and fungal communities, which drive important ecosystem processes but are difficult to characterize across broad spatial scales. In forests, canopy structural diversity may influence soil microorganisms through its effects on ecosystem productivity and root architecture, and via associations between canopy structure, stand age, and species richness. Given that structural diversity is one of the few types of diversity that can be readily measured remotely (e.g., using light detection and ranging—LiDAR), establishing links between structural and microbial diversity could facilitate the detection of belowground biodiversity hotspots. We investigated the potential for using remotely sensed information about forest structural diversity as a predictor of soil microbial community richness and composition. We calculated LiDAR‐derived metrics of structural diversity as well as a suite of stand and soil properties from 38 forested plots across the central hardwoods region of Indiana, USA, to test whether forest canopy structure is linked with the community richness and diversity of four key soil microbial groups: bacteria, fungi, arbuscular mycorrhizal (AM) fungi, and ectomycorrhizal (EM) fungi. We found that the density of canopy vegetation is positively associated with the taxonomic richness (alpha diversity) of EM fungi, independent of changes in plant taxonomic richness. Further, structural diversity metrics were significantly correlated with the overall community composition of bacteria, EM, and total fungal communities. However, soil properties were the strongest predictors of variation in the taxonomic richness and community composition of microbial communities in comparison with structural diversity and tree species diversity. As remote sensing tools and algorithms are rapidly advancing, these results may have important implications for the use of remote sensing of vegetation structural diversity for management and restoration practices aimed at preserving belowground biodiversity.