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Soil as an extended composite phenotype of the microbial metagenome

We use a unique set of terrestrial experiments to demonstrate how soil management practises result in emergence of distinct associations between physical structure and biological functions. These associations have a significant effect on the flux, resilience and efficiency of nutrient delivery to pl...

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Autores principales: Neal, Andrew L., Bacq-Labreuil, Aurélie, Zhang, Xiaoxian, Clark, Ian M., Coleman, Kevin, Mooney, Sacha J., Ritz, Karl, Crawford, John W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7327058/
https://www.ncbi.nlm.nih.gov/pubmed/32606383
http://dx.doi.org/10.1038/s41598-020-67631-0
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author Neal, Andrew L.
Bacq-Labreuil, Aurélie
Zhang, Xiaoxian
Clark, Ian M.
Coleman, Kevin
Mooney, Sacha J.
Ritz, Karl
Crawford, John W.
author_facet Neal, Andrew L.
Bacq-Labreuil, Aurélie
Zhang, Xiaoxian
Clark, Ian M.
Coleman, Kevin
Mooney, Sacha J.
Ritz, Karl
Crawford, John W.
author_sort Neal, Andrew L.
collection PubMed
description We use a unique set of terrestrial experiments to demonstrate how soil management practises result in emergence of distinct associations between physical structure and biological functions. These associations have a significant effect on the flux, resilience and efficiency of nutrient delivery to plants (including water). Physical structure, determining the air–water balance in soil as well as transport rates, is influenced by nutrient and physical interventions. Contrasting emergent soil structures exert selective pressures upon the microbiome metagenome. These selective pressures are associated with the quality of organic carbon inputs, the prevalence of anaerobic microsites and delivery of nutrients to microorganisms attached to soil surfaces. This variety results in distinctive gene assemblages characterising each state. The nature of the interactions provide evidence that soil behaves as an extended composite phenotype of the resident microbiome, responsive to the input and turnover of plant-derived organic carbon. We provide new evidence supporting the theory that soil-microbe systems are self-organising states with organic carbon acting as a critical determining parameter. This perspective leads us to propose carbon flux, rather than soil organic carbon content as the critical factor in soil systems, and we present evidence to support this view.
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spelling pubmed-73270582020-07-01 Soil as an extended composite phenotype of the microbial metagenome Neal, Andrew L. Bacq-Labreuil, Aurélie Zhang, Xiaoxian Clark, Ian M. Coleman, Kevin Mooney, Sacha J. Ritz, Karl Crawford, John W. Sci Rep Article We use a unique set of terrestrial experiments to demonstrate how soil management practises result in emergence of distinct associations between physical structure and biological functions. These associations have a significant effect on the flux, resilience and efficiency of nutrient delivery to plants (including water). Physical structure, determining the air–water balance in soil as well as transport rates, is influenced by nutrient and physical interventions. Contrasting emergent soil structures exert selective pressures upon the microbiome metagenome. These selective pressures are associated with the quality of organic carbon inputs, the prevalence of anaerobic microsites and delivery of nutrients to microorganisms attached to soil surfaces. This variety results in distinctive gene assemblages characterising each state. The nature of the interactions provide evidence that soil behaves as an extended composite phenotype of the resident microbiome, responsive to the input and turnover of plant-derived organic carbon. We provide new evidence supporting the theory that soil-microbe systems are self-organising states with organic carbon acting as a critical determining parameter. This perspective leads us to propose carbon flux, rather than soil organic carbon content as the critical factor in soil systems, and we present evidence to support this view. Nature Publishing Group UK 2020-06-30 /pmc/articles/PMC7327058/ /pubmed/32606383 http://dx.doi.org/10.1038/s41598-020-67631-0 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
Neal, Andrew L.
Bacq-Labreuil, Aurélie
Zhang, Xiaoxian
Clark, Ian M.
Coleman, Kevin
Mooney, Sacha J.
Ritz, Karl
Crawford, John W.
Soil as an extended composite phenotype of the microbial metagenome
title Soil as an extended composite phenotype of the microbial metagenome
title_full Soil as an extended composite phenotype of the microbial metagenome
title_fullStr Soil as an extended composite phenotype of the microbial metagenome
title_full_unstemmed Soil as an extended composite phenotype of the microbial metagenome
title_short Soil as an extended composite phenotype of the microbial metagenome
title_sort soil as an extended composite phenotype of the microbial metagenome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7327058/
https://www.ncbi.nlm.nih.gov/pubmed/32606383
http://dx.doi.org/10.1038/s41598-020-67631-0
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