Long-term forest soil warming alters microbial communities in temperate forest soils

dc.contributor.author DeAngelis, Kristen M.
dc.contributor.author Pold, Grace
dc.contributor.author Topcuoglu, Begum D.
dc.contributor.author van Diepen, Linda T. A.
dc.contributor.author Varney, Rebecca M.
dc.contributor.author Blanchard, Jeffrey L.
dc.contributor.author Melillo, Jerry M.
dc.contributor.author Frey, Serita D.
dc.date.accessioned 2015-04-13T17:52:15Z
dc.date.available 2015-04-13T17:52:15Z
dc.date.issued 2015-02-13
dc.description © The Author(s), 2015. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Frontiers in Microbiology 6 (2015): 104, doi:10.3389/fmicb.2015.00104. en_US
dc.description.abstract Soil microbes are major drivers of soil carbon cycling, yet we lack an understanding of how climate warming will affect microbial communities. Three ongoing field studies at the Harvard Forest Long-term Ecological Research (LTER) site (Petersham, MA) have warmed soils 5°C above ambient temperatures for 5, 8, and 20 years. We used this chronosequence to test the hypothesis that soil microbial communities have changed in response to chronic warming. Bacterial community composition was studied using Illumina sequencing of the 16S ribosomal RNA gene, and bacterial and fungal abundance were assessed using quantitative PCR. Only the 20-year warmed site exhibited significant change in bacterial community structure in the organic soil horizon, with no significant changes in the mineral soil. The dominant taxa, abundant at 0.1% or greater, represented 0.3% of the richness but nearly 50% of the observations (sequences). Individual members of the Actinobacteria, Alphaproteobacteria and Acidobacteria showed strong warming responses, with one Actinomycete decreasing from 4.5 to 1% relative abundance with warming. Ribosomal RNA copy number can obfuscate community profiles, but is also correlated with maximum growth rate or trophic strategy among bacteria. Ribosomal RNA copy number correction did not affect community profiles, but rRNA copy number was significantly decreased in warming plots compared to controls. Increased bacterial evenness, shifting beta diversity, decreased fungal abundance and increased abundance of bacteria with low rRNA operon copy number, including Alphaproteobacteria and Acidobacteria, together suggest that more or alternative niche space is being created over the course of long-term warming. en_US
dc.description.sponsorship This work was supported by funding from the University of Massachusetts Amherst to DeAngelis and the National Science Foundation Long-term Ecological Research (LTER) Program. en_US
dc.format.mimetype application/pdf
dc.identifier.citation Frontiers in Microbiology 6 (2015): 104 en_US
dc.identifier.doi 10.3389/fmicb.2015.00104
dc.identifier.uri https://hdl.handle.net/1912/7209
dc.language.iso en_US en_US
dc.publisher Frontiers Media en_US
dc.relation.uri https://doi.org/10.3389/fmicb.2015.00104
dc.rights Attribution 4.0 International *
dc.rights.uri http://creativecommons.org/licenses/by/4.0/
dc.subject Climate change en_US
dc.subject Microbial ecology en_US
dc.subject Ribosomal RNA en_US
dc.subject rrn operon copy number en_US
dc.subject Trophic strategy en_US
dc.title Long-term forest soil warming alters microbial communities in temperate forest soils en_US
dc.type Article en_US
dspace.entity.type Publication
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