Physics
Scientific paper
Jan 1996
adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=1996gecoa..60..243m&link_type=abstract
Geochimica et Cosmochimica Acta, Volume 60, Issue 2, p. 243-263.
Physics
22
Scientific paper
We have used porewater sampling by in situ techniques, including whole-core squeezing, as well as by shipboard sectioning and whole-core squeezing to estimate the rates of sedimentary organic matter oxidation and CaCO3 dissolution at seven sites on the Ceara Rise in the western equatorial Atlantic Ocean. Porewater NO3- profiles at all sites show a pattern indicative of active organic matter oxidation in the upper 15 20 cm of the sediments and in a buried, organic-rich layer. The organic C oxidation rate generally decreases with increasing water depth, from a value of 22 μmol/cm2/y at the shallowest site (3279 m) to 14 μmol/cm2/y at the deepest site (4675 m). Over this depth range, the bottomwaters vary from moderately supersaturated with respect to calcite to strongly undersaturated. High-resolution alkalinity profiles, measured in porewaters collected by in situ whole-core squeezing, yield estimated Ca2+ fluxes of 11 μmol/cm2/y at a site located at the depth of the calcite saturation horizon, and 7.6 μzmol/cm2/y at a moderately undersaturated site. Ca2+ fluxes calculated from profiles in porewaters collected by relatively coarse-resolution in situ sampling methods clearly indicate that there is CaCO3 dissolution above the calcite saturation horizon. The dissolution of aragonite may contribute to the dissolution flux at the shallowest site. These Ca2+ fluxes, as well as fluxes estimated from a model of sedimentary organic matter oxidation and calcite dissolution, indicate that 36 66% of the CaCO3 rain to the seafloor dissolves at sites at and above the calcite saturation horizon, while 52 75% of the rain dissolves at sites below this depth. When these results are incorporated into the oceanic CaCO3 budget of Milliman 1993, they indicate that 35% of CaCO3 production is preserved in the deep sea; they suggest a CaCO3 accumulation rate that is 27% lower than that estimated by Milliman 1993. Our Corg oxidation/CaCO3 dissolution model indicates that a large fraction of the CaCO3 dissolution that is occurring on the Ceara Rise is attributable to the neutralization of metabolic acids produced during organic matter oxidation. The efficiency with which organic matter oxidation dissolves CaCO3 (that is, the ratio, CaCO3 dissolution attributable to organic matter oxidation:organic matter oxidation rate) generally increases as degree of undersaturation of bottomwaters increases. However, there are deviations from the general trend that can be attributed to site-to-site variations in the kinetics of organic matter oxidation and calcite dissolution. This result indicates that the dissolution of CaCO3 as a result of organic matter oxidation in the deep sea may mask the effects of variations in surface water CaCO3 productivity and bottomwater chemistry on the accumulation rate of CaCO3 in deep-sea sediments.
Martin Robert W.
Sayles Frederick L.
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