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Soil bacterial community structure remains stable over a 5-year chronosequence of insect-induced tree mortality
Extensive tree mortality from insect epidemics has raised concern over possible effects on soil biogeochemical processes. Yet despite the importance of microbes in nutrient cycling, how soil bacterial communities respond to insect-induced tree mortality is largely unknown. We examined soil bacterial...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4267275/ https://www.ncbi.nlm.nih.gov/pubmed/25566204 http://dx.doi.org/10.3389/fmicb.2014.00681 |
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author | Ferrenberg, Scott Knelman, Joseph E. Jones, Jennifer M. Beals, Stower C. Bowman, William D. Nemergut, Diana R. |
author_facet | Ferrenberg, Scott Knelman, Joseph E. Jones, Jennifer M. Beals, Stower C. Bowman, William D. Nemergut, Diana R. |
author_sort | Ferrenberg, Scott |
collection | PubMed |
description | Extensive tree mortality from insect epidemics has raised concern over possible effects on soil biogeochemical processes. Yet despite the importance of microbes in nutrient cycling, how soil bacterial communities respond to insect-induced tree mortality is largely unknown. We examined soil bacterial community structure (via 16S rRNA gene pyrosequencing) and community assembly processes (via null deviation analysis) along a 5-year chronosequence (substituting space for time) of bark beetle-induced tree mortality in the southern Rocky Mountains, USA. We also measured microbial biomass and soil chemistry, and used in situ experiments to assess inorganic nitrogen mineralization rates. We found that bacterial community structure and assembly—which was strongly influenced by stochastic processes—were largely unaffected by tree mortality despite increased soil ammonium ([Formula: see text]) pools and reductions in soil nitrate ([Formula: see text]) pools and net nitrogen mineralization rates after tree mortality. Linear models suggested that microbial biomass and bacterial phylogenetic diversity are significantly correlated with nitrogen mineralization rates of this forested ecosystem. However, given the overall resistance of the bacterial community to disturbance from tree mortality, soil nitrogen processes likely remained relatively stable following tree mortality when considered at larger spatial and longer temporal scales—a supposition supported by the majority of available studies regarding biogeochemical effects of bark beetle infestations in this region. Our results suggest that soil bacterial community resistance to disturbance helps to explain the relatively weak effects of insect-induced tree mortality on soil N and C pools reported across the Rocky Mountains, USA. |
format | Online Article Text |
id | pubmed-4267275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-42672752015-01-06 Soil bacterial community structure remains stable over a 5-year chronosequence of insect-induced tree mortality Ferrenberg, Scott Knelman, Joseph E. Jones, Jennifer M. Beals, Stower C. Bowman, William D. Nemergut, Diana R. Front Microbiol Microbiology Extensive tree mortality from insect epidemics has raised concern over possible effects on soil biogeochemical processes. Yet despite the importance of microbes in nutrient cycling, how soil bacterial communities respond to insect-induced tree mortality is largely unknown. We examined soil bacterial community structure (via 16S rRNA gene pyrosequencing) and community assembly processes (via null deviation analysis) along a 5-year chronosequence (substituting space for time) of bark beetle-induced tree mortality in the southern Rocky Mountains, USA. We also measured microbial biomass and soil chemistry, and used in situ experiments to assess inorganic nitrogen mineralization rates. We found that bacterial community structure and assembly—which was strongly influenced by stochastic processes—were largely unaffected by tree mortality despite increased soil ammonium ([Formula: see text]) pools and reductions in soil nitrate ([Formula: see text]) pools and net nitrogen mineralization rates after tree mortality. Linear models suggested that microbial biomass and bacterial phylogenetic diversity are significantly correlated with nitrogen mineralization rates of this forested ecosystem. However, given the overall resistance of the bacterial community to disturbance from tree mortality, soil nitrogen processes likely remained relatively stable following tree mortality when considered at larger spatial and longer temporal scales—a supposition supported by the majority of available studies regarding biogeochemical effects of bark beetle infestations in this region. Our results suggest that soil bacterial community resistance to disturbance helps to explain the relatively weak effects of insect-induced tree mortality on soil N and C pools reported across the Rocky Mountains, USA. Frontiers Media S.A. 2014-12-16 /pmc/articles/PMC4267275/ /pubmed/25566204 http://dx.doi.org/10.3389/fmicb.2014.00681 Text en Copyright © 2014 Ferrenberg, Knelman, Jones, Beals, Bowman and Nemergut. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Ferrenberg, Scott Knelman, Joseph E. Jones, Jennifer M. Beals, Stower C. Bowman, William D. Nemergut, Diana R. Soil bacterial community structure remains stable over a 5-year chronosequence of insect-induced tree mortality |
title | Soil bacterial community structure remains stable over a 5-year chronosequence of insect-induced tree mortality |
title_full | Soil bacterial community structure remains stable over a 5-year chronosequence of insect-induced tree mortality |
title_fullStr | Soil bacterial community structure remains stable over a 5-year chronosequence of insect-induced tree mortality |
title_full_unstemmed | Soil bacterial community structure remains stable over a 5-year chronosequence of insect-induced tree mortality |
title_short | Soil bacterial community structure remains stable over a 5-year chronosequence of insect-induced tree mortality |
title_sort | soil bacterial community structure remains stable over a 5-year chronosequence of insect-induced tree mortality |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4267275/ https://www.ncbi.nlm.nih.gov/pubmed/25566204 http://dx.doi.org/10.3389/fmicb.2014.00681 |
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