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Phenotypic plasticity of fungal traits in response to moisture and temperature

Phenotypic plasticity of traits is commonly measured in plants to improve understanding of organismal and ecosystem responses to climate change but is far less studied for microbes. Specifically, decomposer fungi are thought to display high levels of phenotypic plasticity and their functions have im...

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Autores principales: Alster, Charlotte J., Allison, Steven D., Johnson, Nels G., Glassman, Sydney I., Treseder, Kathleen K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723763/
https://www.ncbi.nlm.nih.gov/pubmed/36740602
http://dx.doi.org/10.1038/s43705-021-00045-9
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author Alster, Charlotte J.
Allison, Steven D.
Johnson, Nels G.
Glassman, Sydney I.
Treseder, Kathleen K.
author_facet Alster, Charlotte J.
Allison, Steven D.
Johnson, Nels G.
Glassman, Sydney I.
Treseder, Kathleen K.
author_sort Alster, Charlotte J.
collection PubMed
description Phenotypic plasticity of traits is commonly measured in plants to improve understanding of organismal and ecosystem responses to climate change but is far less studied for microbes. Specifically, decomposer fungi are thought to display high levels of phenotypic plasticity and their functions have important implications for ecosystem dynamics. Assessing the phenotypic plasticity of fungal traits may therefore be important for predicting fungal community response to climate change. Here, we assess the phenotypic plasticity of 15 fungal isolates (12 species) from a Southern California grassland. Fungi were incubated on litter at five moisture levels (ranging from 4–50% water holding capacity) and at five temperatures (ranging from 4–36 °C). After incubation, fungal biomass and activities of four extracellular enzymes (cellobiohydrolase (CBH), β-glucosidase (BG), β-xylosidase (BX), and N-acetyl-β-D-glucosaminidase (NAG)) were measured. We used response surface methodology to determine how fungal phenotypic plasticity differs across the moisture-temperature gradient. We hypothesized that fungal biomass and extracellular enzyme activities would vary with moisture and temperature and that the shape of the response surface would vary between fungal isolates. We further hypothesized that more closely related fungi would show more similar response surfaces across the moisture-temperature gradient. In support of our hypotheses, we found that plasticity differed between fungi along the temperature gradient for fungal biomass and for all the extracellular enzyme activities. Plasticity also differed between fungi along the moisture gradient for BG activity. These differences appear to be caused by variation mainly at the moisture and temperature extremes. We also found that more closely related fungi had more similar extracellular enzymes activities at the highest temperature. Altogether, this evidence suggests that with global warming, fungal biodiversity may become increasingly important as functional traits tend to diverge along phylogenetic lines at higher temperatures.
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spelling pubmed-97237632023-01-04 Phenotypic plasticity of fungal traits in response to moisture and temperature Alster, Charlotte J. Allison, Steven D. Johnson, Nels G. Glassman, Sydney I. Treseder, Kathleen K. ISME Commun Article Phenotypic plasticity of traits is commonly measured in plants to improve understanding of organismal and ecosystem responses to climate change but is far less studied for microbes. Specifically, decomposer fungi are thought to display high levels of phenotypic plasticity and their functions have important implications for ecosystem dynamics. Assessing the phenotypic plasticity of fungal traits may therefore be important for predicting fungal community response to climate change. Here, we assess the phenotypic plasticity of 15 fungal isolates (12 species) from a Southern California grassland. Fungi were incubated on litter at five moisture levels (ranging from 4–50% water holding capacity) and at five temperatures (ranging from 4–36 °C). After incubation, fungal biomass and activities of four extracellular enzymes (cellobiohydrolase (CBH), β-glucosidase (BG), β-xylosidase (BX), and N-acetyl-β-D-glucosaminidase (NAG)) were measured. We used response surface methodology to determine how fungal phenotypic plasticity differs across the moisture-temperature gradient. We hypothesized that fungal biomass and extracellular enzyme activities would vary with moisture and temperature and that the shape of the response surface would vary between fungal isolates. We further hypothesized that more closely related fungi would show more similar response surfaces across the moisture-temperature gradient. In support of our hypotheses, we found that plasticity differed between fungi along the temperature gradient for fungal biomass and for all the extracellular enzyme activities. Plasticity also differed between fungi along the moisture gradient for BG activity. These differences appear to be caused by variation mainly at the moisture and temperature extremes. We also found that more closely related fungi had more similar extracellular enzymes activities at the highest temperature. Altogether, this evidence suggests that with global warming, fungal biodiversity may become increasingly important as functional traits tend to diverge along phylogenetic lines at higher temperatures. Nature Publishing Group UK 2021-08-28 /pmc/articles/PMC9723763/ /pubmed/36740602 http://dx.doi.org/10.1038/s43705-021-00045-9 Text en © The Author(s) 2021 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
Alster, Charlotte J.
Allison, Steven D.
Johnson, Nels G.
Glassman, Sydney I.
Treseder, Kathleen K.
Phenotypic plasticity of fungal traits in response to moisture and temperature
title Phenotypic plasticity of fungal traits in response to moisture and temperature
title_full Phenotypic plasticity of fungal traits in response to moisture and temperature
title_fullStr Phenotypic plasticity of fungal traits in response to moisture and temperature
title_full_unstemmed Phenotypic plasticity of fungal traits in response to moisture and temperature
title_short Phenotypic plasticity of fungal traits in response to moisture and temperature
title_sort phenotypic plasticity of fungal traits in response to moisture and temperature
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723763/
https://www.ncbi.nlm.nih.gov/pubmed/36740602
http://dx.doi.org/10.1038/s43705-021-00045-9
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