Factors influencing organic carbon preservation in marine sediments.

The organic matter that escapes decomposition is buried and preserved in marine sediments, with much debate as to whether the amount depends on bottom-water O2 concentration. One group argues that decomposition is more efficient with O2, and hence, organic carbon will be preferentially oxidized in its presence, and preserved in its absence. Another group argues that the kinetics of organic matter decomposition are similar in the presence and absence of O2, and there should be no influence of O2 on preservation. A compilation of carbon preservation shows that both groups are right, depending on the circumstances of deposition. At high rates of deposition, such as near continental margins, little difference in preservation is found with varying bottom-water O2. It is important that most carbon in these sediments decomposes by anaerobic pathways regardless of bottom-water O2. Hence, little influence of bottom-water O2 on preservation would, in fact, be expected. As sedimentation rate drops, sediments deposited under oxygenated bottom water become progressively more aerobic, while euxinic sediments remain anaerobic. Under these circumstances, the relative efficiencies of aerobic and anaerobic decomposition could affect preservation. Indeed, enhanced preservation is observed in low-O2 and euxinic environments. To explore in detail the factors contributing to this enhanced carbon preservation, aspects of the biochemistries of the aerobic and anaerobic process are reviewed. Other potential influences on preservation are also explored. Finally, a new model for organic carbon decomposition, the "pseudo-G" model, is developed. This model couples the degradation of refractory organic matter to the overall metabolic activity of the sediment, and has consequences for carbon preservation due to the mixing together of labile and refractory organic matter by bioturbation.

[1]  B. B. J�rgensen,et al.  Volatile Fatty Acids and Hydrogen as Substrates for Sulfate-Reducing Bacteria in Anaerobic Marine Sediment , 1981, Applied and environmental microbiology.

[2]  T. Blackburn,et al.  The fate of organic carbon and nitrogen in experimental marine sediment systems: Influence of bioturbation and anoxia , 1987 .

[3]  D. Hydes,et al.  Early organic diagenesis: The significance of progressive subsurface oxidation fronts in pelagic sediments , 1985 .

[4]  R. Berner,et al.  The role of sedimentary organic matter in bacterial sulfate reduction: The G model tested1 , 1984 .

[5]  J. Calvin Giddings,et al.  Mineralogical and textural controls on the organic composition of coastal marine sediments: Hydrodynamic separation using SPLITT-fractionation , 1994 .

[6]  Catherine D. Chambers,et al.  In Situ Treatment of Hazardous Waste-Contaminated Soils , 1992 .

[7]  D. Canfield,et al.  Sulfate reduction and oxic respiration in marine sediments: implications for organic carbon preservation in euxinic environments. , 1989, Deep-sea research. Part A, Oceanographic research papers.

[8]  J. Middelburg Organic carbon, sulphur, and iron in recent semi-euxinic sediments of Kau Bay, Indonesia , 1991 .

[9]  J. Murray,et al.  Oxygen Consumption in Pelagic Marine Sediments , 1980, Science.

[10]  C. Reimers,et al.  Carbon fluxes and burial rates over the continental slope and rise off central California with impli , 1992 .

[11]  L. Pratt Influence of Paleoenvironmental Factors on Preservation of Organic Matter in Middle Cretaceous Greenhorn Formation, Pueblo, Colorado , 1984 .

[12]  Robert A. Berner,et al.  Early Diagenesis: A Theoretical Approach , 1980 .

[13]  Bernard P. Boudreau,et al.  A comparison of closed- and open-system models for porewater pH and calcite-saturation state , 1993 .

[14]  R. Bustin,et al.  Influence of water column anoxia on the burial and preservation of carbon and phosphorus in marine shales , 1993 .

[15]  D. Lovley,et al.  Novel Mode of Microbial Energy Metabolism: Organic Carbon Oxidation Coupled to Dissimilatory Reduction of Iron or Manganese , 1988, Applied and environmental microbiology.

[16]  Robert K. Ham,et al.  Stabilization of solid waste in landfills , 1982 .

[17]  Gregory L. Cowie,et al.  Sources and relative reactivities of amino acids, neutral sugars, and lignin in an intermittently anoxic marine environment , 1992 .

[18]  Wallace S. Broecker,et al.  The Carbon cycle and atmospheric CO[2] : natural variations Archean to present , 1985 .

[19]  D. Canfield,et al.  Pathways of organic carbon oxidation in three continental margin sediments. , 1993, Marine geology.

[20]  T. Blackburn,et al.  Coupling of cycles and global significance of sediment diagenesis , 1993 .

[21]  M. Bender,et al.  Fate of organic carbon reaching the deep sea floor: a status report☆ , 1984 .

[22]  G. Cowie,et al.  Biochemical indicators of diagenetic alteration in natural organic matter mixtures , 1994, Nature.

[23]  B. Jørgensen Mineralization of organic matter in the sea bed—the role of sulphate reduction , 1982, Nature.

[24]  C. Smith,et al.  Adding Biology to One-Dimensional Models of Sediment-Carbon Degradation: The Multi-B Approach , 1992 .

[25]  R. Bartha,et al.  The Sulphate-Reducing Bacteria , 1979 .

[26]  Jørgensen BoBarker A comparison of methods for the quantification of bacterial sulfate reduction in coastal marine sediments , 1978 .

[27]  D. Canfield Organic Matter Oxidation in Marine Sediments , 1993 .

[28]  R. Jahnke,et al.  Fine scale distributions of porosity and particulate excess210Pb, organic carbon and CaCO3 in surface sediments of the deep equatorial Pacific , 1986 .

[29]  G. Shimmield,et al.  Lack of enhanced preservation of organic matter in sediments under the oxygen minimum on the Oman Margin , 1992 .

[30]  Timothy M. Vogel,et al.  Incorporation of Oxygen from Water into Toluene and Benzene during Anaerobic Fermentative Transformation , 1986, Applied and environmental microbiology.

[31]  Christophe Rabouille,et al.  Biogeochemical Transformations in Sediments: Kinetic Models of Early Diagenesis , 1993 .

[32]  D. Repeta Carotenoid diagenesis in recent marine sediments: II. Degradation of fucoxanthin to loliolide , 1989 .

[33]  J. Bollag,et al.  Microbial metabolism of homocyclic and heterocyclic aromatic compounds under anaerobic conditions. , 1987, Microbiological reviews.

[34]  W. Reeburgh,et al.  Anaerobic mineralization of marine sediment organic matter: Rates and the role of anaerobic processes in the oceanic carbon economy , 1987 .

[35]  Akira Otsuki,et al.  Production of Dissolved Organic Matter from Dead Green Algal Cells. I. Aerobic Microbial Decomposition , 1972 .

[36]  D. Canfield,et al.  The anaerobic degradation of organic matter in Danish coastal sediments: iron reduction, manganese reduction, and sulfate reduction. , 1993, Geochimica et cosmochimica acta.

[37]  J. Hedges,et al.  Fluxes and reactivities of organic matter in a coastal marine bay , 1988 .

[38]  Cindy Lee Controls on organic carbon preservation: The use of stratified water bodies to compare intrinsic rates of decomposition in oxic and anoxic systems , 1992 .

[39]  J. Middelburg A simple rate model for organic matter decomposition in marine sediments , 1989 .

[40]  J. Hedges,et al.  Processes controlling the organic carbon content of open ocean sediments , 1988 .

[41]  W. Reeburgh Anaerobic methane oxidation: Rate depth distributions in Skan Bay sediments , 1980 .

[42]  M. P. Bryant,et al.  Anaerobic Degradation of Lactate by Syntrophic Associations of Methanosarcina barkeri and Desulfovibrio Species and Effect of H2 on Acetate Degradation , 1981, Applied and environmental microbiology.

[43]  D. Repeta A high resolution historical record of Holocene anoxygenic primary production in the Black Sea , 1993 .

[44]  G. Demaison Anoxia vs. Productivity: What Controls the Formation of Organic-Carbon-Rich Sediments and Sedimentary Rocks?: Discussion , 1991 .

[45]  G. Ourisson,et al.  The Microbial Origin of Fossil Fuels , 1984 .

[46]  A. Devol Methane oxidation rates in the anaerobic sediments of Saanich Inlet1 , 1983 .

[47]  D. Canfield,et al.  Pyrite Formation and Fossil Preservation , 1991 .

[48]  E. Odier,et al.  Degradation of lignin. , 1992 .

[49]  R. Cranston,et al.  Early diagenesis in deep sea turbidites: The imprint of paleo-oxidation zones , 1988 .

[50]  R M Atlas,et al.  Microbial degradation of petroleum hydrocarbons: an environmental perspective , 1981, Microbiological reviews.

[51]  Akira Otsuki,et al.  PRODUCTION OF DISSOLVED ORGANIC MATTER FROM DEAD GREEN ALGAL CELLS. I. AEROBIC MICROBIAL DECOMPOSITION: AEROBIC PRODUCTION OF DOM , 1972 .

[52]  R. Hodson,et al.  Anaerobic Biodegradation of the Lignin and Polysaccharide Components of Lignocellulose and Synthetic Lignin by Sediment Microflora , 1984, Applied and environmental microbiology.

[53]  D. Canfield,et al.  The reactivity of sedimentary iron minerals toward sulfide , 1992 .

[54]  A. Rinzema,et al.  Anaerobic treatment of sulfate containing wastewater. , 1988 .

[55]  R. Bustin,et al.  Lack of evidence for enhanced preservation of sedimentary organic matter in the oxygen minimum of the Gulf of California , 1992 .