2007 GSA Denver Annual Meeting (28–31 October 2007)

Paper No. 9
Presentation Time: 3:30 PM

CALCIUM CARBONATE CYCLING IN ANOXIC OCEANS


HIGGINS, John Andrew, Department of Geosciences, Princeton University, Washington Road, Guyot Hall, Princeton, NJ 08544 and SCHRAG, Daniel P., Earth and Planetary Sciences, Harvard University, 20 Oxford Street, Cambridge, MA 02138, jahiggin@Princeton.EDU

Systematic changes in carbonate sedimentology over Earth history indicate a shift in the locus of abundant CaCO3 precipitation from on to above the seafloor (Grotzinger, 1990).  Oxic respiration of organic carbon leads to undersaturation and dissolution of CaCO3, even in cases where the overlying seawater is supersaturated (Walter & Burton, 1990).  In contrast, anoxic respiration of organic carbon buffers pH, leading to preservation and/or precipitation of CaCO3 (Ben Yaakov et al., 1977).  Because the oxygen content of sediments together with the flux of organic carbon largely determines whether or not sediments dissolve or precipitate CaCO3, changes in O2 and organic carbon cycling over Earth history should be reflected in the sedimentology of carbonate rocks.  Although the evolution of atmospheric O2 is poorly constrained, this hypothesis is broadly consistent with observations of declining seafloor CaCO3 precipitation in the Proterozoic and early Phanerozoic.  Because low values of carbonate mineral saturation negatively affect the energetics of CaCO3 biomineralization, the evolution and episodic demise of skeletal CaCO3 producers may be related to the effect of changes in the O2 content of sediments and the cycling of organic carbon on CaCO3 precipitation on the seafloor.