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Inorganic sulfur turnover in oligohaline estuarine sediments

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Abstract

Inorganic sulfur turnover was examined in oligohaline (salinity < 2 g kg-1) Chesapeake Bay sediments during the summer. Cores incubated for < 3 hr exhibited higher sulfate reduction (SR) rates (13–58 mmol m-2 d-1) than those incubated for 3–8 hr (3–8 mmol m-2 d-1). SR rates (determined with35SO 2-4 ) increased with depth over the top few cm to a maximum at 5 cm, just beneath the boundary between brown and black sediment. SR rates decreased below 5 cm, probably due to sulfate limitation (sulfate < 25 μM). Kinetic experiments yielded an apparent half-saturating sulfate concentration (Ks) of 34 μM, ≈ 20-fold lower than that determined for sediments from the mesohaline region of the estuary. Sulfate loss from water overlying intact cores, predicted on the basis of measured SR rates, was not observed over a 28-hr incubation period. Reduction of35SO 2-4 during diffusion experiments with intact core segments from 0–4 and 5–9 cm horizons was less than predicted by non-steady state diagenetic models based on35SO 2-4 reduction in whole core injection experiments. The results indicate that net sulfate flux into sediments was an order of magnitude lower than the gross sulfur turnover rate. Solid phase reduced inorganic sulfur concentrations were only 2–3 times less than those in sediments from the mesohaline region of the Bay, despite the fact that oligohaline bottom water sulfate concentrations were 10-fold lower. Our results demonstrate the potential for rapid SR in low salinity estuarine sediments, which are inhabited by sulfate-reducing bacteria with a high affinity for sulfate, and in which sulfide oxidation processes replenish the pore water sulfate pool on a time scale of hours.

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Abbreviations

AVS:

acid-volatile sulfide

NAVS:

nonacid-volatile sulfide

SR:

sulfate reduction

SRB:

sulfate-reducing bacteria

References

  • Albert D (1984) Improved techniques for measurement of sulfate reduction and pyrite formation in sediments. Trans. Am. Geophys. Union 45: 906

    Google Scholar 

  • Aller RC (1980) Quantifying solute distributions in the bioturbated zone of marine sediments by defining an average microenvironment. Geochem. Cosmochim. Acta 44: 1955–1965

    Article  Google Scholar 

  • Aller RC & Rude PR (1988) Complete oxidation of solid phase sulfides by manganese and bacteria in anoxic marine sediments. Geochim. Cosmochim. Acta 52: 751–765

    Article  Google Scholar 

  • Bak F & Pfennig N (1991) Microbial sulfate reduction in littoral sediments of Lake Constance. FEMS Microbiol. Ecol. 85: 31–42

    Article  Google Scholar 

  • Baker LA, Urban NR, Brezonik PL & Sherman LA (1989) Sulfur cycling in an experimentally acidified seepage lake. In: Saltzman ES & Cooper WJ (Eds) Biogenic Sulfur in the Environment (pp 79–100). American Chemical Society, Washington, DC

    Google Scholar 

  • Boudreau BP & Westrich JT (1984) The dependence of bacterial sulfate reduction on sulfate concentration in marine sediments. Geochim. Cosmochim. Acta 48: 2503–2516

    Article  Google Scholar 

  • Brown KA (1986) Formation of organic sulphur in anaerobic peat. Soil Biol. Biochem. 18: 131–140

    Article  Google Scholar 

  • Carignan R & Tessier A (1988) The co-diagenesis of sulfur and iron in acid lake sediments of southwestern Quebec. Geochim. Cosmochim. Acta 52: 1179–1188

    Article  Google Scholar 

  • Davison W, Lishman JP & Hilton J (1985) Formation of pyrite in freshwater sediments: Implications for C/S ratios. Geochim. Cosmochim. Acta 49: 1615–1620

    Article  Google Scholar 

  • Drever JI (1982) The Geochemistry of Natural Waters. Prentice-Hall, Englewood Cliffs

    Google Scholar 

  • Emerson S, Jahnke R & Heggie D (1984) Sediment water exchange in shallow estuarine sediments. J. Mar. Res. 42: 709–730

    Article  Google Scholar 

  • Fossing H & Jørgensen BB (1990) Isotope exchange reactions with radiolabeled sulfur compounds in anoxic seawater. Biogeochem. 9: 223–245

    Article  Google Scholar 

  • Fossing H, Thode-Andersen S & Jørgensen BB (1992) Sulfur isotope exchange between35S-labeled inorganic sulfur compounds in anoxic marine sediments. Mar. Chem. 38: 117–132

    Article  Google Scholar 

  • Herlihy AT & Mills AL (1985) Sulfate reduction in freshwater sediments receiving acid mine drainage. Appl. Environ. Microbiol. 49: 179–186

    Google Scholar 

  • Hill JM (1988) Physiographic distribution of interstitial waters in Chesapeake Bay. Report of Investigations No. 49. Maryland Geological Survey. Annapolis, MD

    Google Scholar 

  • Hordijk KA, Hagenaars CPMM & Cappenberg TE (1985) Kinetic studies of bacterial sulfate reduction in freshwater sediments by high-pressure liquid chromatography and microdistillation. Appl. Environ. Microbiol. 49: 434–440

    Google Scholar 

  • Ingvorsen K & Jørgensen BB (1984) Kinetics of sulfate uptake by freshwater and marine species ofDesulfovibrio. Arch. Microbiol. 139: 61–66

    Article  Google Scholar 

  • Ingvorsen K, Zehnder AJB & Jørgensen BB (1984) Kinetics of sulfate and acetate uptake byDesulfobacter postgatei. Appl. Environ. Microbiol. 47: 403–408

    Google Scholar 

  • Ingvorsen K, Zeikus JG & Brock TD (1981) Dynamics of bacterial sulfate reduction in a eutrophic lake. Appl. Environ. Microbiol. 42: 1029–1036

    Google Scholar 

  • Jørgensen BB (1982) Mineralization of organic matter in the sea bed — the role of sulphate reduction. Nature 296: 643–645

    Article  Google Scholar 

  • Jørgensen BB (1990a) The sulfur cycle of freshwater sediments: Role of thiosulfate. Limnol. Oceanogr. 35: 1329–1342

    Google Scholar 

  • Jørgensen BB (1990b) A thiosulfate shunt in the sulfur cycle of marine sediments. Science 249: 152–154

    Article  Google Scholar 

  • Kelly CA & Rudd JWM (1984) Epilimnetic sulfate reduction and its relationship to lake acidification. Biogeochem. 1: 63–77

    Article  Google Scholar 

  • King GM & Klug MJ (1980) Sulfhydrolase activity in sediments of Wintergreen Lake, Kalamazoo County, Michigan. Appl. Environ. Microbiol. 39: 950–956

    Google Scholar 

  • King GM & Klug MJ (1982) Comparative aspects of sulfur mineralization in sediments of a eutrophic lake. Appl. Environ. Microbiol. 43: 1406–1412

    Google Scholar 

  • King GM (1990) Effects of added manganic and ferric oxides on sulfate reduction and sulfide oxidation in intertidal sediments. FEMS Microb. Ecol. 73: 131–138

    Article  Google Scholar 

  • Likens GE, Wright RF, Galloway JN & Butler TJ (1979) Acid rain. Sci. Amer. 241: 43–51

    Google Scholar 

  • Lovley DR & Klug MJ (1983) Sulfate reducers can outcompete methanogens at freshwater sulfate concentrations. Appl. Environ. Microbiol. 45: 187–192

    Google Scholar 

  • Lovley DR & Klug MJ (1986) Model for the distribution of sulfate reduction and methanogenesis in freshwater sediments. Geochim. Cosmochim. Acta 50: 11–18

    Article  Google Scholar 

  • Lovely DR & Phillips EJP (1987) Competitive mechanisms for inhibition of sulfate reduction and methane production in the zone of ferric iron reduction in sediments. Appl. Environ. Microbiol. 53: 2636–2641

    Google Scholar 

  • Marnette ECL, Hordijk CA, Van Breemen N & Cappenberg TE (1992) Sulfate reduction and S-oxidation in a moorland pool sediment. Biogeochemistry 17: 123–143

    Article  Google Scholar 

  • Martens CS & Berner RA (1974) Methane production in the interstitial water of sulfate depleted marine sediments. Science 185: 1167–1169

    Article  Google Scholar 

  • Martens CS & Goldhaber MB (1978) Early diagenesis in transitionary sedimentary environments of the White Oak Estuary, North Carolina. Limnol. Oceanogr. 23: 428–441

    Google Scholar 

  • Oremland RS & Taylor BF (1978) Sulfate reduction and methanogenesis in marine sediments. Geochim. Cosmochim. Acta 42: 209–214

    Article  Google Scholar 

  • Roden EE & Tuttle JH (1993) Inorganic sulfur cycling in mid and lower Chesapeake Bay sediments. Mar. Ecol. Prog. Ser. 93: 101–118

    Google Scholar 

  • Rudd JWM, Kelly CA & Furutani A (1986) The role of sulfate reduction in long term accumulation of organic and inorganic sulfur in lake sediments. Limnol. Oceanogr. 31: 1281–1291

    Google Scholar 

  • Schultze DG (1988) Separation and concentration of iron-containing phases. In: Stucki JW, Goodman BA & Schwertmann (Eds) Iron in Soil and Clay Minerals (pp 63–81). D. Reidel Publishing Co., Dordrecht, Holland

    Google Scholar 

  • Sinke AJ, Cornelese AA, Cappenberg TE & Zehnder JB (1992) Seasonal variation in sulfate reduction and methanogenesis in peaty sediments of eutrophic Lake Loosdrecht, The Netherlands. Biogeochemistry 16: 43–61

    Google Scholar 

  • Spratt HG Jr & Morgan MD (1990) Sulfur cycling in a cedar-dominated, freshwater wetland. Limnol. Oceanogr. 35: 1586–1593

    Article  Google Scholar 

  • Smith RL & Klug MJ (1981) Reduction of sulfur compounds in the sediments of a eutrophic lake basin. Appl. Environ. Microbiol. 41: 1230–1237

    Google Scholar 

  • Truper HG & Schlegel HG (1964) Sulfur metabolism in Thiorhodacca 1. Antonie van Leeuwenhoek J. Microbiol. Serol. 30: 225–238

    Google Scholar 

  • Urban NR (1993) Sulfur retention in lake sediments. In: Baker LA (Ed) Environmental Chemistry of Lakes and Reservoirs (in press). American Chemical Society, Washington

  • Urban NR, Brezonik PL, Baker LA & Sherman LA (1993) Sulfate reduction and diffusion in sediments of Little Rock Lake, Wisconsin. Limnol. Oceanogr. In press

  • Weider RK & Lang GE (1988) Cycling of inorganic and organic sulfur in peat from Big Run Bog, West Virginia. Biogeochem. 5: 221–242

    Article  Google Scholar 

  • Weider RK, Yavitt JB & Lang GE (1990) Methane production and sulfate reduction in two Appalachian peatlands. Biogeochem. 10: 81–104

    Google Scholar 

  • White JR, Gubala CP, Fry B, Owen J & Mitchell MJ (1989) Sediment biogeochemistry of iron and sulfur in an acidic lake. Geochim. Cosmochim. Acta 53: 2547–2559

    Article  Google Scholar 

  • Williams PJ (1973) The validity of the application of simple kinetic analysis to heterogeneous microbial populations. Limnol. Oceanogr. 18: 159–165

    Google Scholar 

  • Winfrey MR & Zeikus JG (1977) Effect of sulfate on carbon and electron flow during microbial methanogenesis in freshwater sediments. Appl. Environ. Microbiol. 33: 275–281

    Google Scholar 

  • Wright RT & Hobbie JE (1965) The uptake of organic solutes in lake water. Limnol. Oceanogr. 10: 22–28

    Google Scholar 

  • Zhabina NN & Volkov II (1978) A method of determination of various sulfur compounds in sea sediment and rocks. In: Krumbein (Ed) Environmental Biogeochemistry and Geomicrobiology, Vol. 3 (pp 735–746). Ann Arbor Sci. Publ., Ann Arbor

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Roden, E.E., Tuttle, J.H. Inorganic sulfur turnover in oligohaline estuarine sediments. Biogeochemistry 22, 81–105 (1993). https://doi.org/10.1007/BF00002706

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