4.5 Article

Mapping electron sources and sinks in a marine biogeobattery

Journal

JOURNAL OF GEOPHYSICAL RESEARCH-BIOGEOSCIENCES
Volume 119, Issue 8, Pages 1475-1486

Publisher

AMER GEOPHYSICAL UNION
DOI: 10.1002/2014JG002673

Keywords

biogeobattery; cable bacteria; self-potential

Funding

  1. European Research Council under the European Union [291650]
  2. Danish National Research Foundation [DNRF104]
  3. Danish Council for Independent Research/Natural Sciences
  4. DOE Office of Science (BER), U.S. Department of Energy [DE-FG02-08ER646559, DE-SC0007118]
  5. Chevron Energy Technology Company [CW852844, K26625]
  6. U.S. Department of Energy (DOE) [DE-SC0007118] Funding Source: U.S. Department of Energy (DOE)
  7. European Research Council (ERC) [291650] Funding Source: European Research Council (ERC)

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Filamentous, multicellular bacteria of the Desulfobulbaceae family form a biogeobattery in marine sediments by mediating an electric coupling between sulfide oxidation in deeper anoxic layers and oxygen reduction at the sediment surface. The electric fields generated in such biogeobatteries were determined with microelectrodes and correlated well with geochemical indicators of microbial electrogenic activity in the top 2 cm of the sediment. The electric fields collapsed within less than a minute when oxygen was removed and reestablished when oxygen was reintroduced, demonstrating a direct coupling between aerobic microbial activity and presence of electric fields. Modeling of the electric potential distribution was used to quantify and localize electron sources and sinks. Most anodic oxidation was confined to the lower part of the anoxic zone with nondetectable free sulfide, suggesting that iron sulfide was the main sulfide source and had already been depleted in the upper part of the anoxic zone. The flow of electrons from anoxic sediment layers fuelled up to 80% of the aerobic activity of the sediment. Responses of the electric field to the presence and absence of nitrate, nitrite, or nitrous oxide in the overlying water readily demonstrated potentials for cathodic reduction of nitrite or nitric oxide and possibly nitrate but not nitrous oxide.

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