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Abstract Root‐associated fungi, particularly ectomycorrhizal fungi (EMF), are critical symbionts of all boreal tree species. Although climatically driven increases in wildfire frequency and extent have been hypothesized to increase vegetation transitions from tundra to boreal forest, fire reduces mycorrhizal inoculum. Therefore, changes in mycobiont inoculum may potentially limit tree‐seedling establishment beyond current treeline. We investigated whether ectomycorrhizal shrubs that resprout after fire support similar fungal taxa to those that associate with tree seedlings that establish naturally after fire. We then assessed whether mycobiont identity correlates with the biomass or nutrient status of these tree seedlings. The majority of fungal taxa observed on shrub and seedling root systems wereEMF, with some dark septate endophytes and ericoid mycorrhizal taxa. Seedlings and adjacent shrubs associated with similar arrays of fungal taxa, and there were strong correlations between the structure of seedling and shrub fungal communities. These results show that resprouting postfire shrubs support fungal taxa compatible with tree seedlings that establish after wildfire. Shrub taxon, distance to the nearest shrub and fire severity influenced the similarity between seedling and shrub fungal communities. Fungal composition was correlated with both foliar C:N ratio and seedling biomass and was one of the strongest explanatory variables predicting seedling biomass. While correlative, these results suggest that mycobionts are important to nutrient acquisition and biomass accrual of naturally establishing tree seedlings at treeline and that mycobiont taxa shared by resprouting postfire vegetation may be a significant source of inoculum for tree‐seedling establishment beyond current treeline.
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Wildfire impacts on root‐associated fungi and predicted plant–soil feedbacks in the boreal forest: Research progress and recommendations
Root-associated fungi play a critical role in plant ecophysiology, growth and subsequent responses to disturbances, so they are thought to be particularly instrumental in shaping vegetation dynamics after fire in the boreal forest. Despite increasing data on the distribution of fungal taxonomic diversity through space and time in boreal ecosystems, there are knowledge gaps with respect to linking these patterns to ecosystem function and process. Here we explore what is currently known about postfire root-associated fungi in the boreal forest. We focus on wildfire impacts on mycorrhizal fungi and the relationships between plant–fungal interactions and forest recovery in an effort to explore whether postfire mycorrhizal dynamics underlie plant–soil feedbacks that may influence fire-facilitated vegetation shifts. We characterize the mechanisms by which wildfire influences root-associated fungal community assembly. We identify scenarios of postfire plant–fungal interactions that represent putative positive and negative plant–soil feedbacks that may impact successional trajectories. We highlight the need for empirical field observations and experiments to inform our ability to translate patterns of postfire root-associated fungal diversity to ecological function and application in models. We suggest that understanding postfire interactions between root-associated fungi and plants is critical to predict fire effects on vegetation patterns, ecosystem function, future landscape flammability and feedbacks to climate.
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- Award ID(s):
- 1636476
- PAR ID:
- 10399368
- Date Published:
- Journal Name:
- Functional Ecology
- ISSN:
- 0269-8463
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1111/1365-2435.14205
