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      Marine Deep Biosphere Microbial Communities Assemble in Near-Surface Sediments in Aarhus Bay

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          Abstract

          Analyses of microbial diversity in marine sediments have identified a core set of taxa unique to the marine deep biosphere. Previous studies have suggested that these specialized communities are shaped by processes in the surface seabed, in particular that their assembly is associated with the transition from the bioturbated upper zone to the nonbioturbated zone below. To test this hypothesis, we performed a fine-scale analysis of the distribution and activity of microbial populations within the upper 50 cm of sediment from Aarhus Bay (Denmark). Sequencing and qPCR were combined to determine the depth distributions of bacterial and archaeal taxa (16S rRNA genes) and sulfate-reducing microorganisms (SRM) ( dsrB gene). Mapping of radionuclides throughout the sediment revealed a region of intense bioturbation at 0–6 cm depth. The transition from bioturbated sediment to the subsurface below (7 cm depth) was marked by a shift from dominant surface populations to common deep biosphere taxa (e.g., Chloroflexi and Atribacteria). Changes in community composition occurred in parallel to drops in microbial activity and abundance caused by reduced energy availability below the mixed sediment surface. These results offer direct evidence for the hypothesis that deep subsurface microbial communities present in Aarhus Bay mainly assemble already centimeters below the sediment surface, below the bioturbation zone.

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          Early oxidation of organic matter in pelagic sediments of the eastern equatorial Atlantic: suboxic diagenesis

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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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              Quantifying community assembly processes and identifying features that impose them.

              Spatial turnover in the composition of biological communities is governed by (ecological) Drift, Selection and Dispersal. Commonly applied statistical tools cannot quantitatively estimate these processes, nor identify abiotic features that impose these processes. For interrogation of subsurface microbial communities distributed across two geologically distinct formations of the unconfined aquifer underlying the Hanford Site in southeastern Washington State, we developed an analytical framework that advances ecological understanding in two primary ways. First, we quantitatively estimate influences of Drift, Selection and Dispersal. Second, ecological patterns are used to characterize measured and unmeasured abiotic variables that impose Selection or that result in low levels of Dispersal. We find that (i) Drift alone consistently governs ∼25% of spatial turnover in community composition; (ii) in deeper, finer-grained sediments, Selection is strong (governing ∼60% of turnover), being imposed by an unmeasured but spatially structured environmental variable; (iii) in shallower, coarser-grained sediments, Selection is weaker (governing ∼30% of turnover), being imposed by vertically and horizontally structured hydrological factors;(iv) low levels of Dispersal can govern nearly 30% of turnover and be caused primarily by spatial isolation resulting from limited exchange between finer and coarser-grain sediments; and (v) highly permeable sediments are associated with high levels of Dispersal that homogenize community composition and govern over 20% of turnover. We further show that our framework provides inferences that cannot be achieved using preexisting approaches, and suggest that their broad application will facilitate a unified understanding of microbial communities.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                12 April 2019
                2019
                : 10
                : 758
                Affiliations
                [1] 1Center for Geomicrobiology, Department of Bioscience, Aarhus University , Aarhus, Denmark
                [2] 2Department of Biogeochemistry, Max Planck Institute for Marine Microbiology , Bremen, Germany
                Author notes

                Edited by: Peter R. Girguis, Harvard University, United States

                Reviewed by: Sonja Kristine Fagervold, UMS2348 Observatoire Océanologique de Banyuls-sur-Mer (OOB), France; Meng Li, Shenzhen University, China

                *Correspondence: Caitlin Petro, cpetro@ 123456gatech.edu

                These authors have contributed equally to this work

                Present address: Caitlin Petro, Georgia Institute of Technology, School of Biological Sciences, Atlanta, GA, United States Birthe Zäncker, Marine Biological Association of the United Kingdom, Plymouth, United Kingdom

                This article was submitted to Aquatic Microbiology, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2019.00758
                6474314
                31031732
                88b09334-4f0d-4edc-9322-45991a5d9538
                Copyright © 2019 Petro, Zäncker, Starnawski, Jochum, Ferdelman, Jørgensen, Røy, Kjeldsen and Schramm.

                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) and the copyright owner(s) 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.

                History
                : 18 January 2019
                : 26 March 2019
                Page count
                Figures: 6, Tables: 0, Equations: 0, References: 76, Pages: 13, Words: 0
                Funding
                Funded by: Danmarks Grundforskningsfond 10.13039/501100001732
                Award ID: DNRF104
                Funded by: European Research Council 10.13039/501100000781
                Award ID: #294200, 593 MICROENERGY
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                marine sediment,16s rrna,dsrb,biodiversity,sulfate reducing microorganisms,microbial community assembly

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