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Experimentally determined traits shape bacterial community composition one and five years following wildfire
Wildfires represent major ecological disturbances, burning 2–3% of Earth’s terrestrial area each year with sometimes drastic effects above- and belowground. Soil bacteria offer an ideal, yet understudied system within which to explore fundamental principles of fire ecology. To understand how wildfir...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10482699/ https://www.ncbi.nlm.nih.gov/pubmed/37524797 http://dx.doi.org/10.1038/s41559-023-02135-4 |
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author | Johnson, Dana B. Woolet, Jamie Yedinak, Kara M. Whitman, Thea |
author_facet | Johnson, Dana B. Woolet, Jamie Yedinak, Kara M. Whitman, Thea |
author_sort | Johnson, Dana B. |
collection | PubMed |
description | Wildfires represent major ecological disturbances, burning 2–3% of Earth’s terrestrial area each year with sometimes drastic effects above- and belowground. Soil bacteria offer an ideal, yet understudied system within which to explore fundamental principles of fire ecology. To understand how wildfires restructure soil bacterial communities and alter their functioning, we sought to translate aboveground fire ecology to belowground systems by determining which microbial traits are important post-fire and whether changes in bacterial communities affect carbon cycling. We employed an uncommon approach to assigning bacterial traits, by first running three laboratory experiments to directly determine which microbes survive fires, grow quickly post-fire and/or thrive in the post-fire environment, while tracking CO(2) emissions. We then quantified the abundance of taxa assigned to each trait in a large field dataset of soils one and five years after wildfires in the boreal forest of northern Canada. We found that fast-growing bacteria rapidly dominate post-fire soils but return to pre-burn relative abundances by five years post-fire. Although both fire survival and affinity for the post-fire environment were statistically significant predictors of post-fire community composition, neither are particularly influential. Our results from the incubation trials indicate that soil carbon fluxes post-wildfire are not likely limited by microbial communities, suggesting strong functional resilience. From these findings, we offer a traits-based framework of bacterial responses to wildfire. |
format | Online Article Text |
id | pubmed-10482699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104826992023-09-08 Experimentally determined traits shape bacterial community composition one and five years following wildfire Johnson, Dana B. Woolet, Jamie Yedinak, Kara M. Whitman, Thea Nat Ecol Evol Article Wildfires represent major ecological disturbances, burning 2–3% of Earth’s terrestrial area each year with sometimes drastic effects above- and belowground. Soil bacteria offer an ideal, yet understudied system within which to explore fundamental principles of fire ecology. To understand how wildfires restructure soil bacterial communities and alter their functioning, we sought to translate aboveground fire ecology to belowground systems by determining which microbial traits are important post-fire and whether changes in bacterial communities affect carbon cycling. We employed an uncommon approach to assigning bacterial traits, by first running three laboratory experiments to directly determine which microbes survive fires, grow quickly post-fire and/or thrive in the post-fire environment, while tracking CO(2) emissions. We then quantified the abundance of taxa assigned to each trait in a large field dataset of soils one and five years after wildfires in the boreal forest of northern Canada. We found that fast-growing bacteria rapidly dominate post-fire soils but return to pre-burn relative abundances by five years post-fire. Although both fire survival and affinity for the post-fire environment were statistically significant predictors of post-fire community composition, neither are particularly influential. Our results from the incubation trials indicate that soil carbon fluxes post-wildfire are not likely limited by microbial communities, suggesting strong functional resilience. From these findings, we offer a traits-based framework of bacterial responses to wildfire. Nature Publishing Group UK 2023-07-31 2023 /pmc/articles/PMC10482699/ /pubmed/37524797 http://dx.doi.org/10.1038/s41559-023-02135-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Johnson, Dana B. Woolet, Jamie Yedinak, Kara M. Whitman, Thea Experimentally determined traits shape bacterial community composition one and five years following wildfire |
title | Experimentally determined traits shape bacterial community composition one and five years following wildfire |
title_full | Experimentally determined traits shape bacterial community composition one and five years following wildfire |
title_fullStr | Experimentally determined traits shape bacterial community composition one and five years following wildfire |
title_full_unstemmed | Experimentally determined traits shape bacterial community composition one and five years following wildfire |
title_short | Experimentally determined traits shape bacterial community composition one and five years following wildfire |
title_sort | experimentally determined traits shape bacterial community composition one and five years following wildfire |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10482699/ https://www.ncbi.nlm.nih.gov/pubmed/37524797 http://dx.doi.org/10.1038/s41559-023-02135-4 |
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