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Plant community stability is associated with a decoupling of prokaryote and fungal soil networks
Soil microbial networks play a crucial role in plant community stability. However, we lack knowledge on the network topologies associated with stability and the pathways shaping these networks. In a 13-year mesocosm experiment, we determined links between plant community stability and soil microbial...
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/PMC10287681/ https://www.ncbi.nlm.nih.gov/pubmed/37349286 http://dx.doi.org/10.1038/s41467-023-39464-8 |
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author | in ‘t Zandt, Dina Kolaříková, Zuzana Cajthaml, Tomáš Münzbergová, Zuzana |
author_facet | in ‘t Zandt, Dina Kolaříková, Zuzana Cajthaml, Tomáš Münzbergová, Zuzana |
author_sort | in ‘t Zandt, Dina |
collection | PubMed |
description | Soil microbial networks play a crucial role in plant community stability. However, we lack knowledge on the network topologies associated with stability and the pathways shaping these networks. In a 13-year mesocosm experiment, we determined links between plant community stability and soil microbial networks. We found that plant communities on soil abandoned from agricultural practices 60 years prior to the experiment promoted destabilising properties and were associated with coupled prokaryote and fungal soil networks. This coupling was mediated by strong interactions of plants and microbiota with soil resource cycling. Conversely, plant communities on natural grassland soil exhibited a high stability, which was associated with decoupled prokaryote and fungal soil networks. This decoupling was mediated by a large variety of past plant community pathways shaping especially fungal networks. We conclude that plant community stability is associated with a decoupling of prokaryote and fungal soil networks and mediated by plant-soil interactions. |
format | Online Article Text |
id | pubmed-10287681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102876812023-06-24 Plant community stability is associated with a decoupling of prokaryote and fungal soil networks in ‘t Zandt, Dina Kolaříková, Zuzana Cajthaml, Tomáš Münzbergová, Zuzana Nat Commun Article Soil microbial networks play a crucial role in plant community stability. However, we lack knowledge on the network topologies associated with stability and the pathways shaping these networks. In a 13-year mesocosm experiment, we determined links between plant community stability and soil microbial networks. We found that plant communities on soil abandoned from agricultural practices 60 years prior to the experiment promoted destabilising properties and were associated with coupled prokaryote and fungal soil networks. This coupling was mediated by strong interactions of plants and microbiota with soil resource cycling. Conversely, plant communities on natural grassland soil exhibited a high stability, which was associated with decoupled prokaryote and fungal soil networks. This decoupling was mediated by a large variety of past plant community pathways shaping especially fungal networks. We conclude that plant community stability is associated with a decoupling of prokaryote and fungal soil networks and mediated by plant-soil interactions. Nature Publishing Group UK 2023-06-22 /pmc/articles/PMC10287681/ /pubmed/37349286 http://dx.doi.org/10.1038/s41467-023-39464-8 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 in ‘t Zandt, Dina Kolaříková, Zuzana Cajthaml, Tomáš Münzbergová, Zuzana Plant community stability is associated with a decoupling of prokaryote and fungal soil networks |
title | Plant community stability is associated with a decoupling of prokaryote and fungal soil networks |
title_full | Plant community stability is associated with a decoupling of prokaryote and fungal soil networks |
title_fullStr | Plant community stability is associated with a decoupling of prokaryote and fungal soil networks |
title_full_unstemmed | Plant community stability is associated with a decoupling of prokaryote and fungal soil networks |
title_short | Plant community stability is associated with a decoupling of prokaryote and fungal soil networks |
title_sort | plant community stability is associated with a decoupling of prokaryote and fungal soil networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287681/ https://www.ncbi.nlm.nih.gov/pubmed/37349286 http://dx.doi.org/10.1038/s41467-023-39464-8 |
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