Wildfires, which are increasing in frequency and severity with climate change, reduce soil microbial biomass and alter microbial community composition and function. The soil microbiome plays a vital role in carbon (C) and nitrogen (N) cycling, but its complexity makes it challenging to predict post-wildfire soil microbial dynamics and resulting impacts on ecosystem biogeochemistry. The application of biogeochemically relevant conceptual trait-based frameworks to the soil microbiome can distill this complexity, enabling enhanced predictability of soil microbiome recovery following wildfire and subsequent impacts to biogeochemical cycles. Conceptual frameworks that have direct links to soil C and N cycling have been developed for the soil microbiome; the Y-A-S framework overviews soil microbiome life history strategies that have tradeoffs with one another and others have proposed frameworks specific to wildfire. Here, we aimed to delineate post-wildfire changes of bacterial traits in western US coniferous forests to inform how severe wildfire influences soil microbiome recovery and resultant biogeochemical cycling. We utilized a comprehensive metagenome-assembled genome catalog from post-wildfire soils representing 1 to 11 years following low- and high-severity burning to identify traits that enable the persistence of microbial taxa in burned soils and influence ecosystem C and N cycling. We found that high-severity wildfire initially selects for fast growers and, up to a decade post-fire, taxa that invest in genes for acquiring diverse resources from the external environment, which in combination could increase soil C losses. This work begins to disentangle how climate change–induced shifts in wildfire behavior might alter microbially mediated soil biogeochemical cycling.
Nelson, Amelia R., et al. "Wildfire impact on soil microbiome life history traits and roles in ecosystem carbon cycling." ISME Communications, vol. 4, no. 1, Aug. 2024. https://doi.org/10.1093/ismeco/ycae108
Nelson, Amelia R., Rhoades, Charles C., Fegel, Timothy S., Roth, Holly K., Caiafa, Marcos V., Glassman, Sydney I., Borch, Thomas, & Wilkins, Michael J. (2024). Wildfire impact on soil microbiome life history traits and roles in ecosystem carbon cycling. ISME Communications, 4(1). https://doi.org/10.1093/ismeco/ycae108
Nelson, Amelia R., Rhoades, Charles C., Fegel, Timothy S., et al., "Wildfire impact on soil microbiome life history traits and roles in ecosystem carbon cycling," ISME Communications 4, no. 1 (2024), https://doi.org/10.1093/ismeco/ycae108
@article{osti_2447027,
author = {Nelson, Amelia R. and Rhoades, Charles C. and Fegel, Timothy S. and Roth, Holly K. and Caiafa, Marcos V. and Glassman, Sydney I. and Borch, Thomas and Wilkins, Michael J.},
title = {Wildfire impact on soil microbiome life history traits and roles in ecosystem carbon cycling},
annote = {Abstract Wildfires, which are increasing in frequency and severity with climate change, reduce soil microbial biomass and alter microbial community composition and function. The soil microbiome plays a vital role in carbon (C) and nitrogen (N) cycling, but its complexity makes it challenging to predict post-wildfire soil microbial dynamics and resulting impacts on ecosystem biogeochemistry. The application of biogeochemically relevant conceptual trait-based frameworks to the soil microbiome can distill this complexity, enabling enhanced predictability of soil microbiome recovery following wildfire and subsequent impacts to biogeochemical cycles. Conceptual frameworks that have direct links to soil C and N cycling have been developed for the soil microbiome; the Y-A-S framework overviews soil microbiome life history strategies that have tradeoffs with one another and others have proposed frameworks specific to wildfire. Here, we aimed to delineate post-wildfire changes of bacterial traits in western US coniferous forests to inform how severe wildfire influences soil microbiome recovery and resultant biogeochemical cycling. We utilized a comprehensive metagenome-assembled genome catalog from post-wildfire soils representing 1 to 11 years following low- and high-severity burning to identify traits that enable the persistence of microbial taxa in burned soils and influence ecosystem C and N cycling. We found that high-severity wildfire initially selects for fast growers and, up to a decade post-fire, taxa that invest in genes for acquiring diverse resources from the external environment, which in combination could increase soil C losses. This work begins to disentangle how climate change–induced shifts in wildfire behavior might alter microbially mediated soil biogeochemical cycling.},
doi = {10.1093/ismeco/ycae108},
url = {https://www.osti.gov/biblio/2447027},
journal = {ISME Communications},
issn = {ISSN 2730-6151},
number = {1},
volume = {4},
place = {United States},
publisher = {Oxford University Press},
year = {2024},
month = {08}}