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Interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales
It has been widely accepted that there is a distance‐decay pattern in the soil microbiome. However, few studies have attempted to interpret the microbial distance‐decay pattern from the perspective of quantifying underlying processes. In this study, we examined the processes governing bacterial comm...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741136/ https://www.ncbi.nlm.nih.gov/pubmed/31074596 http://dx.doi.org/10.1002/mbo3.851 |
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author | Feng, Maomao Tripathi, Binu M. Shi, Yu Adams, Jonathan M. Zhu, Yong‐Guan Chu, Haiyan |
author_facet | Feng, Maomao Tripathi, Binu M. Shi, Yu Adams, Jonathan M. Zhu, Yong‐Guan Chu, Haiyan |
author_sort | Feng, Maomao |
collection | PubMed |
description | It has been widely accepted that there is a distance‐decay pattern in the soil microbiome. However, few studies have attempted to interpret the microbial distance‐decay pattern from the perspective of quantifying underlying processes. In this study, we examined the processes governing bacterial community assembly at multiple spatial scales in maize fields of Northeast China using Illumina MiSeq sequencing. Results showed that the processes governing spatial turnover in bacterial community composition shifted regularly with spatial scale, with homogenizing dispersal dominating at small spatial scales and variable selection dominating at larger scales, which in turn explained the distance‐decay pattern that closer located sites tended to have higher community similarity. Together, homogenizing dispersal and dispersal limitation resulting from geographic factors governed about 33% of spatial turnover in bacterial community composition. Deterministic selection processes had the strongest influence, at 57%, with biotic factors and abiotic environmental filtering (mainly imposed by soil pH) respectively contributing about 37% and 63% of variation. Our results provided a novel and comprehensive way to explain the distance‐decay pattern of soil microbiome via quantifying the assembly processes at multiple spatial scales, as well as the method to quantify the influence of abiotic, biotic, and geographic factors in shaping microbial community structure, thus enabling understanding of widely acknowledged microbial biogeographic patterns and microbial ecology. |
format | Online Article Text |
id | pubmed-6741136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67411362019-09-13 Interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales Feng, Maomao Tripathi, Binu M. Shi, Yu Adams, Jonathan M. Zhu, Yong‐Guan Chu, Haiyan Microbiologyopen Original Articles It has been widely accepted that there is a distance‐decay pattern in the soil microbiome. However, few studies have attempted to interpret the microbial distance‐decay pattern from the perspective of quantifying underlying processes. In this study, we examined the processes governing bacterial community assembly at multiple spatial scales in maize fields of Northeast China using Illumina MiSeq sequencing. Results showed that the processes governing spatial turnover in bacterial community composition shifted regularly with spatial scale, with homogenizing dispersal dominating at small spatial scales and variable selection dominating at larger scales, which in turn explained the distance‐decay pattern that closer located sites tended to have higher community similarity. Together, homogenizing dispersal and dispersal limitation resulting from geographic factors governed about 33% of spatial turnover in bacterial community composition. Deterministic selection processes had the strongest influence, at 57%, with biotic factors and abiotic environmental filtering (mainly imposed by soil pH) respectively contributing about 37% and 63% of variation. Our results provided a novel and comprehensive way to explain the distance‐decay pattern of soil microbiome via quantifying the assembly processes at multiple spatial scales, as well as the method to quantify the influence of abiotic, biotic, and geographic factors in shaping microbial community structure, thus enabling understanding of widely acknowledged microbial biogeographic patterns and microbial ecology. John Wiley and Sons Inc. 2019-05-10 /pmc/articles/PMC6741136/ /pubmed/31074596 http://dx.doi.org/10.1002/mbo3.851 Text en © 2019 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Feng, Maomao Tripathi, Binu M. Shi, Yu Adams, Jonathan M. Zhu, Yong‐Guan Chu, Haiyan Interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales |
title | Interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales |
title_full | Interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales |
title_fullStr | Interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales |
title_full_unstemmed | Interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales |
title_short | Interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales |
title_sort | interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741136/ https://www.ncbi.nlm.nih.gov/pubmed/31074596 http://dx.doi.org/10.1002/mbo3.851 |
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