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      Dynamics of microbial populations mediating biogeochemical cycling in a freshwater lake

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          Abstract

          Background

          Microbial processes are intricately linked to the depletion of oxygen in in-land and coastal water bodies, with devastating economic and ecological consequences. Microorganisms deplete oxygen during biomass decomposition, degrading the habitat of many economically important aquatic animals. Microbes then turn to alternative electron acceptors, which alter nutrient cycling and generate potent greenhouse gases. As oxygen depletion is expected to worsen with altered land use and climate change, understanding how chemical and microbial dynamics impact dead zones will aid modeling efforts to guide remediation strategies. More work is needed to understand the complex interplay between microbial genes, populations, and biogeochemistry during oxygen depletion.

          Results

          Here, we used 16S rRNA gene surveys, shotgun metagenomic sequencing, and a previously developed biogeochemical model to identify genes and microbial populations implicated in major biogeochemical transformations in a model lake ecosystem. Shotgun metagenomic sequencing was done for one time point in Aug., 2013, and 16S rRNA gene sequencing was done for a 5-month time series (Mar.–Aug., 2013) to capture the spatiotemporal dynamics of genes and microorganisms mediating the modeled processes. Metagenomic binning analysis resulted in many metagenome-assembled genomes (MAGs) that are implicated in the modeled processes through gene content similarity to cultured organism and the presence of key genes involved in these pathways. The MAGs suggested some populations are capable of methane and sulfide oxidation coupled to nitrate reduction. Using the model, we observe that modulating these processes has a substantial impact on overall lake biogeochemistry. Additionally, 16S rRNA gene sequences from the metagenomic and amplicon libraries were linked to processes through the MAGs. We compared the dynamics of microbial populations in the water column to the model predictions. Many microbial populations involved in primary carbon oxidation had dynamics similar to the model, while those associated with secondary oxidation processes deviated substantially.

          Conclusions

          This work demonstrates that the unique capabilities of resident microbial populations will substantially impact the concentration and speciation of chemicals in the water column, unless other microbial processes adjust to compensate for these differences. It further highlights the importance of the biological aspects of biogeochemical processes, such as fluctuations in microbial population dynamics. Integrating gene and population dynamics into biogeochemical models has the potential to improve predictions of the community response under altered scenarios to guide remediation efforts.

          Electronic supplementary material

          The online version of this article (10.1186/s40168-018-0556-7) contains supplementary material, which is available to authorized users.

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          Most cited references53

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          Ferrozine---a new spectrophotometric reagent for iron

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            Patterns and processes of microbial community assembly.

            Recent research has expanded our understanding of microbial community assembly. However, the field of community ecology is inaccessible to many microbial ecologists because of inconsistent and often confusing terminology as well as unnecessarily polarizing debates. Thus, we review recent literature on microbial community assembly, using the framework of Vellend (Q. Rev. Biol. 85:183-206, 2010) in an effort to synthesize and unify these contributions. We begin by discussing patterns in microbial biogeography and then describe four basic processes (diversification, dispersal, selection, and drift) that contribute to community assembly. We also discuss different combinations of these processes and where and when they may be most important for shaping microbial communities. The spatial and temporal scales of microbial community assembly are also discussed in relation to assembly processes. Throughout this review paper, we highlight differences between microbes and macroorganisms and generate hypotheses describing how these differences may be important for community assembly. We end by discussing the implications of microbial assembly processes for ecosystem function and biodiversity.
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              Microbial diversity and soil functions

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                Author and article information

                Contributors
                karoraw1@jhu.edu
                scott.olesen@gmail.com
                ben.scandella@alum.mit.edu
                kyledmit@gmail.com
                sjspen@gmail.com
                e.myers@columbia.edu
                sonaliabraham214@gmail.com
                asookla1@jhu.edu
                410-516-6632 , sprehei1@jhu.edu
                Journal
                Microbiome
                Microbiome
                Microbiome
                BioMed Central (London )
                2049-2618
                18 September 2018
                18 September 2018
                2018
                : 6
                : 165
                Affiliations
                [1 ]ISNI 0000 0001 2171 9311, GRID grid.21107.35, Department of Environmental Health and Engineering, , Johns Hopkins University, ; Baltimore, MD USA
                [2 ]ISNI 0000 0001 2341 2786, GRID grid.116068.8, Department of Biological Engineering, , Massachusetts Institute of Technology, ; Cambridge, MA USA
                [3 ]ISNI 0000 0001 2341 2786, GRID grid.116068.8, Department of Civil and Environmental Engineering, , Massachusetts Institute of Technology, ; Cambridge, MA USA
                [4 ]ISNI 000000041936754X, GRID grid.38142.3c, Present address: Department of Immunology and Infectious Diseases, , Harvard T. H. Chan School of Public Health, ; Boston, MA USA
                [5 ]ISNI 0000 0000 9632 6718, GRID grid.19006.3e, Present address: Institute of the Environment and Sustainability, , University of California, ; Los Angeles, CA USA
                [6 ]ISNI 0000000419368729, GRID grid.21729.3f, Present address: Earth and Environmental Sciences, , Columbia University, ; Palisades, NY USA
                [7 ]Present address: Oregon Water Resources Department, Salem, OR USA
                [8 ]ISNI 000000041936754X, GRID grid.38142.3c, Harvard John A. Paulson School of Engineering and Applied Sciences, ; Cambridge, MA USA
                Author information
                http://orcid.org/0000-0001-7365-2382
                Article
                556
                10.1186/s40168-018-0556-7
                6145348
                30227897
                f3605c85-7b6e-4a56-96c8-da5a0e76776a
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 29 May 2018
                : 5 September 2018
                Categories
                Research
                Custom metadata
                © The Author(s) 2018

                biogeochemical model,16s rrna gene sequencing,metagenome-assembled genome

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