Takacs, K. G. and Borowski, W. S. (2003): Authigenic sulfide mineralization induced by anaerobic methane oxidation in methane-rich, gas-hydrate-associated sediments; stratigraphic patterns of sulfide-sulfur concentration and sulfide-sulfur isotopic composition

Leg/Site/Hole:
ODP 164
ODP 164 995
Identifier:
2005-075325
georefid

Creator:
Takacs, K. G.
Eastern Kentucky University, Department of Earth Sciences, Richmond, KY, United States
author

Borowski, W. S.
author

Identification:
Authigenic sulfide mineralization induced by anaerobic methane oxidation in methane-rich, gas-hydrate-associated sediments; stratigraphic patterns of sulfide-sulfur concentration and sulfide-sulfur isotopic composition
2003
In: Anonymous, Geological Society of America, South-Central Section, 37th annual meeting; Geological Society of America, Southeastern Section, 52nd annual meeting
Geological Society of America (GSA), Boulder, CO, United States
35
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Active sulfide mineralization occurs at the sulfate-methane interface (SMI) in modern, deep-water, continental-margin sediments that overlie accumulations of methane gas hydrate at the Blake Ridge (southeastern North America). Sulfide minerals (elemental sulfur, S degrees ; iron monosulfides, approximately FeS; and pyrite, FeS (sub 2) ) at the present-day sulfate-methane interface are enriched in (super 34) S relative to sulfide minerals in the sulfate reduction zone. These enrichments of (super 34) S occur because of focused anaerobic methane oxidation (AMO) at the SMI carried out by a consortium of methanotrophs and sulfate-reducing microbes, and because of non-steady-state diagenesis. (super 34) S enrichments are a potential diagenetic indicator identifying occurrences of high methane delivery to the sulfate-methane interface and the action of the AMO consortium. A key question is: Are these enrichments of (super 34) S preserved in the sedimentary record? We extracted sulfide sulfur from authigenic sulfide minerals contained in sediments collected at Site 995, Ocean Drilling Program (ODP) Leg 164. Chromium reduction was used to extract sulfide sulfur and we measured sulfide sulfur concentration using iodometric titration. In separate extractions, we precipitated sulfide sulfur as Ag (sub 2) S for sulfur isotopic analysis. Sulfide mineral concentration at the present-day sulfate-methane interface occurring at approximately 20 m is as high as 0.57 wt % sulfur. Preliminary data from the depth interval of 20 to 703.80 m (sediments >0.085 to 6.0 Ma in age) show sulfide concentration ranging from 0.04 to 1.03 wt % sulfur. Twenty-six percent of samples (8 of 30) show sulfide sulfur concentrations higher than that of the present-day SMI. This implies that the diagenetic front at the SMI was stratigraphically stable for longer periods of time, and/or that methane flux to the SMI was higher than observed today. Isotopic data show that (super 34) S enrichments within sulfide minerals persist in the geologic record, and we infer that these enrichments identify SMIs that occurred in the geologic past.
English
Coverage:Geographic coordinates:
North:31.4812
West:-75.3118East: -75.3118
South:31.4812

Geochemistry of rocks, soils, and sediments; aliphatic hydrocarbons; alkanes; anaerobic environment; Atlantic Ocean; authigenic minerals; Blake-Bahama Outer Ridge; continental margin sedimentation; deep-water environment; enrichment; gas hydrates; geochemistry; hydrocarbons; isotopes; Leg 164; methane; North Atlantic; Ocean Drilling Program; ODP Site 995; organic compounds; oxidation; S-34; sedimentation; stable isotopes; sulfates; sulfides; sulfur; titration;

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