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Soil fungal networks maintain local dominance of ectomycorrhizal trees

The mechanisms regulating community composition and local dominance of trees in species-rich forests are poorly resolved, but the importance of interactions with soil microbes is increasingly acknowledged. Here, we show that tree seedlings that interact via root-associated fungal hyphae with soils b...

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Autores principales: Liang, Minxia, Johnson, David, Burslem, David F. R. P., Yu, Shixiao, Fang, Miao, Taylor, Joe D., Taylor, Andy F. S., Helgason, Thorunn, Liu, Xubing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250933/
https://www.ncbi.nlm.nih.gov/pubmed/32457288
http://dx.doi.org/10.1038/s41467-020-16507-y
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author Liang, Minxia
Johnson, David
Burslem, David F. R. P.
Yu, Shixiao
Fang, Miao
Taylor, Joe D.
Taylor, Andy F. S.
Helgason, Thorunn
Liu, Xubing
author_facet Liang, Minxia
Johnson, David
Burslem, David F. R. P.
Yu, Shixiao
Fang, Miao
Taylor, Joe D.
Taylor, Andy F. S.
Helgason, Thorunn
Liu, Xubing
author_sort Liang, Minxia
collection PubMed
description The mechanisms regulating community composition and local dominance of trees in species-rich forests are poorly resolved, but the importance of interactions with soil microbes is increasingly acknowledged. Here, we show that tree seedlings that interact via root-associated fungal hyphae with soils beneath neighbouring adult trees grow faster and have greater survival than seedlings that are isolated from external fungal mycelia, but these effects are observed for species possessing ectomycorrhizas (ECM) and not arbuscular mycorrhizal (AM) fungi. Moreover, survival of naturally-regenerating AM seedlings over ten years is negatively related to the density of surrounding conspecific plants, while survival of ECM tree seedlings displays positive density dependence over this interval, and AM seedling roots contain greater abundance of pathogenic fungi than roots of ECM seedlings. Our findings show that neighbourhood interactions mediated by beneficial and pathogenic soil fungi regulate plant demography and community structure in hyperdiverse forests.
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spelling pubmed-72509332020-06-04 Soil fungal networks maintain local dominance of ectomycorrhizal trees Liang, Minxia Johnson, David Burslem, David F. R. P. Yu, Shixiao Fang, Miao Taylor, Joe D. Taylor, Andy F. S. Helgason, Thorunn Liu, Xubing Nat Commun Article The mechanisms regulating community composition and local dominance of trees in species-rich forests are poorly resolved, but the importance of interactions with soil microbes is increasingly acknowledged. Here, we show that tree seedlings that interact via root-associated fungal hyphae with soils beneath neighbouring adult trees grow faster and have greater survival than seedlings that are isolated from external fungal mycelia, but these effects are observed for species possessing ectomycorrhizas (ECM) and not arbuscular mycorrhizal (AM) fungi. Moreover, survival of naturally-regenerating AM seedlings over ten years is negatively related to the density of surrounding conspecific plants, while survival of ECM tree seedlings displays positive density dependence over this interval, and AM seedling roots contain greater abundance of pathogenic fungi than roots of ECM seedlings. Our findings show that neighbourhood interactions mediated by beneficial and pathogenic soil fungi regulate plant demography and community structure in hyperdiverse forests. Nature Publishing Group UK 2020-05-26 /pmc/articles/PMC7250933/ /pubmed/32457288 http://dx.doi.org/10.1038/s41467-020-16507-y Text en © The Author(s) 2020 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/.
spellingShingle Article
Liang, Minxia
Johnson, David
Burslem, David F. R. P.
Yu, Shixiao
Fang, Miao
Taylor, Joe D.
Taylor, Andy F. S.
Helgason, Thorunn
Liu, Xubing
Soil fungal networks maintain local dominance of ectomycorrhizal trees
title Soil fungal networks maintain local dominance of ectomycorrhizal trees
title_full Soil fungal networks maintain local dominance of ectomycorrhizal trees
title_fullStr Soil fungal networks maintain local dominance of ectomycorrhizal trees
title_full_unstemmed Soil fungal networks maintain local dominance of ectomycorrhizal trees
title_short Soil fungal networks maintain local dominance of ectomycorrhizal trees
title_sort soil fungal networks maintain local dominance of ectomycorrhizal trees
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250933/
https://www.ncbi.nlm.nih.gov/pubmed/32457288
http://dx.doi.org/10.1038/s41467-020-16507-y
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