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Cold seeps in Monterey Bay, California: Geochemistry of pore waters and relationship to benthic foraminiferal calcite
Authors:Joris Gieskes  Anthony E Rathburn  Jonathan B Martin  M Elena Prez  Chris Mahn  Joan M Bernhard  Shelley Day
Institution:a Scripps Institution of Oceanography, IOD-0208, 9500 Gilman Drive, La Jolla, CA 92093-0208, United States;b Indiana State University, Department of Earth and Environmental Systems, Terre Haute, IN 47809, United States;c University of Florida, Department of Geological Sciences, Gainesville, FL 32611-2120, United States;d The Natural History Museum, Department of Palaeontology, Cromwell Road, London SW7 5BD, United Kingdom;e Woods Hole Oceanographic Institution, Geology and Geophysics Department, MS52, Woods Hole, MA 02543, United States
Abstract:An extensive geochemical and biogeochemical examination of CH4 seeps in the Clam Flats area of Monterey Bay provides insight into the character of relationships between seep geochemistry and benthic foraminiferal geochemistry. The area is characterized by sulfide-rich fluids. Sulfide increases are associated with large increases in alkalinity, as well as small decreases in dissolved Ca and Mg. In addition, only small increases in NH4 are observed, but values of δ13C of dissolved inorganic C are as low as ?60‰ at shallow depths (<3 cm). These observations indicate that all these processes are related to the bacterial oxidation of CH4, which is transported upward by slow seepage of pore fluids. The geochemistry of the pore fluids should be relevant to the geochemistry of the carbonate tests of living and dead foraminifera. However, a profound disequilibrium of approximately an order of magnitude occurs between the δ13C values of stained (cytoplasm-containing) foraminiferal carbonate and the C isotope values of ambient pore water dissolved inorganic C. Reasons are unclear for this isotopic disequilibrium, but have important implications for interpretations of foraminiferal carbonate as a paleoenvironmental proxy. Much fine scale work is needed to fully understand the relationships between the biogeochemistry of benthic foraminifera and the geochemistry of the pore waters where they live.
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