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Tradeoffs in hyphal traits determine mycelium architecture in saprobic fungi

The fungal mycelium represents the essence of the fungal lifestyle, and understanding how a mycelium is constructed is of fundamental importance in fungal biology and ecology. Previous studies have examined initial developmental patterns or focused on a few strains, often mutants of model species, a...

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Autores principales: Lehmann, Anika, Zheng, Weishuang, Soutschek, Katharina, Roy, Julien, Yurkov, Andrey M., Rillig, Matthias C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775140/
https://www.ncbi.nlm.nih.gov/pubmed/31578362
http://dx.doi.org/10.1038/s41598-019-50565-7
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author Lehmann, Anika
Zheng, Weishuang
Soutschek, Katharina
Roy, Julien
Yurkov, Andrey M.
Rillig, Matthias C.
author_facet Lehmann, Anika
Zheng, Weishuang
Soutschek, Katharina
Roy, Julien
Yurkov, Andrey M.
Rillig, Matthias C.
author_sort Lehmann, Anika
collection PubMed
description The fungal mycelium represents the essence of the fungal lifestyle, and understanding how a mycelium is constructed is of fundamental importance in fungal biology and ecology. Previous studies have examined initial developmental patterns or focused on a few strains, often mutants of model species, and frequently grown under non-harmonized growth conditions; these factors currently collectively hamper systematic insights into rules of mycelium architecture. To address this, we here use a broader suite of fungi (31 species including members of the Ascomycota, Basidiomycota and Mucoromycota), all isolated from the same soil, and tested for ten architectural traits under standardized laboratory conditions. We find great variability in traits among the saprobic fungal species, and detect several clear tradeoffs in mycelial architecture, for example between internodal length and hyphal diameter. Within the constraints so identified, we document otherwise great versatility in mycelium architecture in this set of fungi, and there was no evidence of trait ‘syndromes’ as might be expected. Our results point to an important dimension of fungal properties with likely consequences for coexistence within local communities, as well as for functional complementarity (e.g. decomposition, soil aggregation).
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spelling pubmed-67751402019-10-09 Tradeoffs in hyphal traits determine mycelium architecture in saprobic fungi Lehmann, Anika Zheng, Weishuang Soutschek, Katharina Roy, Julien Yurkov, Andrey M. Rillig, Matthias C. Sci Rep Article The fungal mycelium represents the essence of the fungal lifestyle, and understanding how a mycelium is constructed is of fundamental importance in fungal biology and ecology. Previous studies have examined initial developmental patterns or focused on a few strains, often mutants of model species, and frequently grown under non-harmonized growth conditions; these factors currently collectively hamper systematic insights into rules of mycelium architecture. To address this, we here use a broader suite of fungi (31 species including members of the Ascomycota, Basidiomycota and Mucoromycota), all isolated from the same soil, and tested for ten architectural traits under standardized laboratory conditions. We find great variability in traits among the saprobic fungal species, and detect several clear tradeoffs in mycelial architecture, for example between internodal length and hyphal diameter. Within the constraints so identified, we document otherwise great versatility in mycelium architecture in this set of fungi, and there was no evidence of trait ‘syndromes’ as might be expected. Our results point to an important dimension of fungal properties with likely consequences for coexistence within local communities, as well as for functional complementarity (e.g. decomposition, soil aggregation). Nature Publishing Group UK 2019-10-02 /pmc/articles/PMC6775140/ /pubmed/31578362 http://dx.doi.org/10.1038/s41598-019-50565-7 Text en © The Author(s) 2019 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
Lehmann, Anika
Zheng, Weishuang
Soutschek, Katharina
Roy, Julien
Yurkov, Andrey M.
Rillig, Matthias C.
Tradeoffs in hyphal traits determine mycelium architecture in saprobic fungi
title Tradeoffs in hyphal traits determine mycelium architecture in saprobic fungi
title_full Tradeoffs in hyphal traits determine mycelium architecture in saprobic fungi
title_fullStr Tradeoffs in hyphal traits determine mycelium architecture in saprobic fungi
title_full_unstemmed Tradeoffs in hyphal traits determine mycelium architecture in saprobic fungi
title_short Tradeoffs in hyphal traits determine mycelium architecture in saprobic fungi
title_sort tradeoffs in hyphal traits determine mycelium architecture in saprobic fungi
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775140/
https://www.ncbi.nlm.nih.gov/pubmed/31578362
http://dx.doi.org/10.1038/s41598-019-50565-7
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