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The impact of electrogenic sulfur oxidation on the biogeochemistry of coastal sediments: A field study
- Source :
- Geochimica et cosmochimica acta, 194, Geochimica et Cosmochimica Acta, Geochimica et Cosmochimica Acta, 2016, 194, pp.211-232. ⟨10.1016/j.gca.2016.08.038⟩, Geochimica et Cosmochimica Acta, Elsevier, 2016, 194, pp.211-232. ⟨10.1016/j.gca.2016.08.038⟩
- Publication Year :
- 2016
- Publisher :
- Elsevier BV, 2016.
-
Abstract
- Electro-active sediments distinguish themselves from other sedimentary environments by the presence of microbially induced electrical currents in the surface layer of the sediment. The electron transport is generated by metabolic activity of long filamentous cable bacteria, in a process referred to as electrogenic sulfur oxidation (e-SOx). Laboratory experiments have shown that e-SOx exerts a large impact on the sediment geochemistry, but its influence on the in situ geochemistry of marine sediments has not been previously investigated. Here, we document the biogeochemical cycling associated with e-SOx in a cohesive coastal sediment in the North Sea (Station 130, Belgian Coastal Zone) during three campaigns (January, March and May 2014). Fluorescence in situ hybridization showed that cable bacteria were present in high densities throughout the sampling period, and that filaments penetrated up to 7 cm deep in the sediment, which is substantially deeper than previously recorded. High resolution microsensor profiling (pH, H2S and O2) revealed the typical geochemical fingerprint of e-SOx, with a wide separation (up to 4.8 cm) between the depth of oxygen penetration and the depth of sulfide appearance. The metabolic activity of cable bacteria induced a current density of 25–32 mA m−2 and created an electrical field of 12–17 mV m−1 in the upper centimeters of the sediment. This electrical field created an ionic drift, which strongly affected the depth profiles and fluxes of major cations (Ca2+, Fe2+) and anions (SO42−) in the pore water. The strong acidification of the pore water at depth resulted in the dissolution of calcium carbonates and iron sulfides, thus leading to a strong accumulation of iron, calcium and manganese in the pore water. While sulfate accumulated in the upper centimeters, no significant effect of e-SOx was found on ammonium, phosphate and silicate depth profiles. Overall, our results demonstrate that cable bacteria can strongly modulate the sedimentary biogeochemical cycling under in situ conditions.
- Subjects :
- 0301 basic medicine
Biogeochemical cycle
010504 meteorology & atmospheric sciences
Sulfide
01 natural sciences
03 medical and health sciences
chemistry.chemical_compound
Pore water pressure
Geochemistry and Petrology
14. Life underwater
Sulfate
ComputingMilieux_MISCELLANEOUS
0105 earth and related environmental sciences
chemistry.chemical_classification
Bacteria
Biogeochemistry
Sediment
redox cycling
6. Clean water
Silicate
[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry
electrogenic sulfur oxidation
030104 developmental biology
cable bacteria
chemistry
Environmental chemistry
Sedimentary rock
marine sediments
long-distance electron transport
Sciences exactes et naturelles
Subjects
Details
- ISSN :
- 00167037
- Volume :
- 194
- Database :
- OpenAIRE
- Journal :
- Geochimica et Cosmochimica Acta
- Accession number :
- edsair.doi.dedup.....7ff36986c2d585c79393433f62c18f24