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The interaction networks formed by ectomycorrhizal fungi (EMF) and their tree hosts, which are important to both forest recruitment and ecosystem carbon and nutrient retention, may be particularly susceptible to climate change at the boreal–temperate forest ecotone where environmental conditions are changing rapidly. Here, we quantified the compositional and functional trait responses of EMF communities and their interaction networks with two boreal (Pinus banksianaandBetula papyrifera) and two temperate (Pinus strobusandQuercus macrocarpa) hosts to a factorial combination of experimentally elevated temperatures and reduced rainfall in a long-term open-air field experiment. The study was conducted at the B4WarmED (Boreal Forest Warming at an Ecotone in Danger) experiment in Minnesota, USA, where infrared lamps and buried heating cables elevate temperatures (ambient, +3.1 °C) and rain-out shelters reduce growing season precipitation (ambient, ~30% reduction). EMF communities were characterized and interaction networks inferred from metabarcoding of fungal-colonized root tips. Warming and rainfall reduction significantly altered EMF community composition, leading to an increase in the relative abundance of EMF with contact-short distance exploration types. These compositional changes, which likely limited the capacity for mycelial connections between trees, corresponded with shifts from highly redundant EMF interaction networks under ambient conditions to less redundant (more specialized) networks. Further, the observed changes in EMF communities and interaction networks were correlated with changes in soil moisture and host photosynthesis. Collectively, these results indicate that the projected changes in climate will likely lead to significant shifts in the traits, structure, and integrity of EMF communities as well as their interaction networks in forest ecosystems at the boreal–temperate ecotone.

 

Rising atmospheric carbon dioxide concentrations (CO₂) and atmospheric nitrogen (N) deposition have contrasting effects on ectomycorrhizal (EM) and arbuscular mycorrhizal (AM) symbioses, potentially mediating forest responses to environmental change.

In this study, we evaluated the cumulative effects of historical environmental change on N concentrations and δ¹⁵N values in AM plants, EM plants, EM fungi, and saprotrophic fungi using herbarium specimens collected in Minnesota, USA from 1871 to 2016. To better understand mycorrhizal mediation of foliar δ¹⁵N, we also analyzed a subset of previously published foliar δ¹⁵N values from across the United States to parse the effects of N deposition and CO₂rise.

Over the last century in Minnesota, N concentrations declined among all groups except saprotrophic fungi. δ¹⁵N also declined among all groups of plants and fungi; however, foliar δ¹⁵N declined less in EM plants than in AM plants. In the analysis of previously published foliar δ¹⁵N values, this slope difference between EM and AM plants was better explained by nitrogen deposition than by CO₂rise.

Mycorrhizal type did not explain trajectories of plant N concentrations. Instead, plants and EM fungi exhibited similar declines in N concentrations, consistent with declining forest N status despite moderate levels of N deposition.

 

Abstract Ecosystems across the globe receive elevated inputs of nutrients, but the consequences of this for soil fungal guilds that mediate key ecosystem functions remain unclear. We find that nitrogen and phosphorus addition to 25 grasslands distributed across four continents promotes the relative abundance of fungal pathogens, suppresses mutualists, but does not affect saprotrophs. Structural equation models suggest that responses are often indirect and primarily mediated by nutrient-induced shifts in plant communities. Nutrient addition also reduces co-occurrences within and among fungal guilds, which could have important consequences for belowground interactions. Focusing only on plots that received no nutrient addition, soil properties influence pathogen abundance globally, whereas plant community characteristics influence mutualists, and climate influence saprotrophs. We show consistent, guild-level responses that enhance our ability to predict shifts in soil function related to anthropogenic eutrophication, which can have longer-term consequences for plant communities. 

Purpose A better knowledge of how deadwood decomposes is critical for accurately characterizing carbon and nutrient cycling in forests. Fungi dominate this decomposition process, but we still have limited understanding of fungal community structuring that ultimately controls the fate of wood decomposition. This is particularly true in tropical ecosystems. To address this knowledge gap, our study capitalized on an extreme storm event that caused a large and synchronized input of deadwood to the forest floor. Methods Here we report data for the first year of wood decomposition of trees in a Puerto Rican dry forest for nine tree species that were snapped by Hurricane Maria in 2017. We measured wood properties and the associated fungal communities after 12 months of decomposition and compared them with initial wood properties and stem-inhabiting fungal communities to identify the best predictors of wood decomposition rates and chemical changes. Results Changes in wood chemistry were primarily explained by rapid xylan losses, the main hemicellulose component for the studied tree species. Fungal communities were dominated by saprotrophic and plant pathogenic fungi and showed moderate changes over time. The initial relative abundances and ratios of different fungal functional guilds were significant predictors of both xylan and glucan losses, with plant pathogenic fungi accelerating cellulose and hemicellulose decomposition rates compared to saprotrophs. Conclusion Our results confirm that fungi present at the time of treefall are strong drivers of wood decomposition and suggest that plant pathogenic fungi might act as efficient early decomposers of hemicellulose in dry tropical forests.