Evidence for microbial iron reduction in the methanic sediments of the oligotrophic southeastern Mediterranean continental shelf
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Published:2019-08-23
Issue:16
Volume:16
Page:3165-3181
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ISSN:1726-4189
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Container-title:Biogeosciences
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language:en
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Short-container-title:Biogeosciences
Author:
Vigderovich Hanni,Liang Lewen,Herut Barak,Wang Fengping,Wurgaft Eyal,Rubin-Blum Maxim,Sivan Orit
Abstract
Abstract. Dissimilatory iron reduction is probably one of the oldest types of
metabolisms that still participates in important biogeochemical cycles, such
as those of carbon and sulfur. It is one of the more energetically favorable
anaerobic microbial respiration processes and is usually coupled to the
oxidation of organic matter. Traditionally this process is thought to be
limited to the shallow part of the sedimentary column in most aquatic
systems. However, iron reduction has also been observed in the methanic zone
of many marine and freshwater sediments, well below its expected zone and occasionally accompanied by decreases in methane, suggesting a link between
the iron and the methane cycles. Nevertheless, the mechanistic nature of this
link (competition, redox or other) has yet to be established and has not
been studied in oligotrophic shallow marine sediments. In this study we
present combined geochemical and molecular evidences for microbial iron
reduction in the methanic zone of the oligotrophic southeastern (SE)
Mediterranean continental shelf. Geochemical porewater profiles indicate
iron reduction in two zones, the uppermost part of the sediment, and the
deeper zone, in the layer of high methane concentration. Results from a
slurry incubation experiment indicate that the deep methanic iron reduction
is microbially mediated. The sedimentary profiles of microbial abundance and
quantitative PCR (qPCR) of the mcrA gene, together with Spearman correlation between
the microbial data and Fe(II) concentrations in the porewater, suggest types
of potential microorganisms that may be involved in the iron reduction via
several potential pathways: H2 or organic matter oxidation, an active
sulfur cycle, or iron-driven anaerobic oxidation of methane. We suggest that
significant upward migration of methane in the sedimentary column and its
oxidation by sulfate may fuel the microbial activity in the sulfate methane
transition zone (SMTZ). The biomass created by this microbial activity can be used by the iron reducers below, in the methanic zone of the sediments of the SE Mediterranean.
Publisher
Copernicus GmbH
Subject
Earth-Surface Processes,Ecology, Evolution, Behavior and Systematics
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