TY - JOUR
T1 - Benthic fluxes and porewater concentration profiles of dissolved organic carbon in sediments from the North Carolina continental slope
AU - Alperin, Marc J.
AU - Martens, Christopher S.
AU - Albert, Daniel B.
AU - Suayah, Ismail B.
AU - Benninger, Larry K.
AU - Blair, Neal E.
AU - Jahnke, Richard A.
N1 - Funding Information:
We thank our numerous colleagues who contributed ideas and data to this study: Joan Willey provided the inspiration and prototype for the porewater sipper, Bob Aller suggested testing the effect of temperature on porewater DOC, Jeff White conducted the sulfate analyses, Krista Walter provided sulfur data, Gayle Plaia identified the polychaete worms used in the centrifugation test, Howard Mendlovitz measured organic carbon concentrations, C:N values, and stable isotope ratios, Larry Mayer graciously provided surface area data for the inter-laboratory comparison, David Burdige shared his DOC benthic flux data and provided many helpful discussions and reviews, Mark Green provided porewater calcium data, and Tamara Pease and Carol Hee helped in the field with sediment processing. We also thank the crews of the R/V Cape Hatteras and R/V Edwin Link/DWS Johnson Sea-Link I for their support and assistance at sea. Finally, we thank Carol Arnosti and Tori Hoehler for their thoughtful comments on an earlier draft of this paper. Funding for this work was provided by the National Science Foundation (OCE96-33456 [CSM, MJA, DBA], OCE96-17297 [RAJ], and OCE93-01793 [NEB]), Department of Energy (DE-FG05-95ER62073 [CSM, MJA, DBA], DE-FG05-92ER61413 [LKB, IBS], and DE-FG05-95ER62036 [RAJ]), and National Undersea Research Center (NOAA NA 36 RU 0060-02, subcontract 9428.1 [LKB, RAJ]).
PY - 1999/2
Y1 - 1999/2
N2 - Numerous studies of marine environments show that dissolved organic carbon (DOC) concentrations in sediments are typically tenfold higher than in the overlying water. Large concentration gradients near the sediment-water interface suggest that there may be a significant flux of organic carbon from sediments to the water column. Furthermore, accumulation of DOC in the porewater may influence the burial and preservation of organic matter by promoting geopolymerization and/or adsorption reactions. We measured DOC concentration profiles (for porewater collected by centrifugation and 'sipping') and benthic fluxes (with in situ and shipboard chambers) at two sites on the North Carolina continental slope to better understand the controls on porewater DOC concentrations and quantify sediment-water exchange rates. We also measured a suite of sediment properties (e.g., sediment accumulation and bioturbation rates, organic carbon content, and mineral surface area) that allow us to examine the relationship between porewater DOC concentrations and organic carbon preservation. Sediment depth-distributions of DOC from a downslope transect (300-1000 m water depth) follow a trend consistent with other porewater constituents (ΣCO2 and SO42-) and a tracer of modern, fine-grained sediment (fallout Pu), suggesting that DOC levels are regulated by organic matter remineralization. However, remineralization rates appear to be relatively uniform across the sediment transect. A simple diagenetic model illustrates that variations in DOC profiles at this site may be due to differences in the depth of the active remineralization zone, which in turn is largely controlled by the intensity of bioturbation. Comparison of porewater DOC concentrations, organic carbon burial efficiency, and organic matter sorption suggest that DOC levels are not a major factor in promoting organic matter preservation or loading on grain surfaces. The DOC benthic fluxes are difficult to detect, but suggest that only 2% of the dissolved organic carbon escapes remineralization in the sediments by transport across the sediment-water interface.
AB - Numerous studies of marine environments show that dissolved organic carbon (DOC) concentrations in sediments are typically tenfold higher than in the overlying water. Large concentration gradients near the sediment-water interface suggest that there may be a significant flux of organic carbon from sediments to the water column. Furthermore, accumulation of DOC in the porewater may influence the burial and preservation of organic matter by promoting geopolymerization and/or adsorption reactions. We measured DOC concentration profiles (for porewater collected by centrifugation and 'sipping') and benthic fluxes (with in situ and shipboard chambers) at two sites on the North Carolina continental slope to better understand the controls on porewater DOC concentrations and quantify sediment-water exchange rates. We also measured a suite of sediment properties (e.g., sediment accumulation and bioturbation rates, organic carbon content, and mineral surface area) that allow us to examine the relationship between porewater DOC concentrations and organic carbon preservation. Sediment depth-distributions of DOC from a downslope transect (300-1000 m water depth) follow a trend consistent with other porewater constituents (ΣCO2 and SO42-) and a tracer of modern, fine-grained sediment (fallout Pu), suggesting that DOC levels are regulated by organic matter remineralization. However, remineralization rates appear to be relatively uniform across the sediment transect. A simple diagenetic model illustrates that variations in DOC profiles at this site may be due to differences in the depth of the active remineralization zone, which in turn is largely controlled by the intensity of bioturbation. Comparison of porewater DOC concentrations, organic carbon burial efficiency, and organic matter sorption suggest that DOC levels are not a major factor in promoting organic matter preservation or loading on grain surfaces. The DOC benthic fluxes are difficult to detect, but suggest that only 2% of the dissolved organic carbon escapes remineralization in the sediments by transport across the sediment-water interface.
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U2 - 10.1016/S0016-7037(99)00032-0
DO - 10.1016/S0016-7037(99)00032-0
M3 - Article
AN - SCOPUS:0032875837
VL - 63
SP - 427
EP - 448
JO - Geochmica et Cosmochimica Acta
JF - Geochmica et Cosmochimica Acta
SN - 0016-7037
IS - 3-4
ER -