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Biogeochemical cycling of sulfur and iron in sediments of a south-east Asian mangrove, Phuket Island, Thailand

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Abstract

Benthic sulfate reduction and sediment pools of sulfur and iron were examined during January 1992 at 3 stations in the Ao Nam Bor mangrove, Phuket, Thailand. Patterns of sulfate reduction rates (0–53 cm) reflected differences in physical and biological conditions at the 3 stations, and highest rates were found at the vegetated site within the mangrove (Rhizophora apiculata) forest. Due to extended oxidation of mangrove sediments, a large portion of the added35S-label was recovered in the chromium reducible pools (FeS2 and S0) (41–91% of the reduced sulfur). Pyrite was the most important inorganic sulfur component, attaining pool sizes 50–100 times higher than acid volatile pools (FeS). HCl-extractable (0.5 M HCl) iron pools, including Fe(II)HCl and Fe(III)HCl, were generally low and Fe(III)HCl was only present in the upper surface layers (0–5 cm). Maximum concentrations of dissolved Fe2+ (35–285 μM) occurred just about the depth where dissolved ΣH2S accumulated. Furthermore Fe2+ and ΣH2S coexisted only where concentrations of both were low. There was an accumulation of organic sulfur in the deep sediment at 2 stations in the inner part of the mangrove. The reoxidation of reduced sulfides was rapid, and storage of sulfur was minor in the upper sediment layers, where factors like bioturbation, the presence of roots, or tidal mixing enhance oxidation processes.

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References

  • Alongi DM (1989) The role of soft-bottom benthic communities in tropical mangrove and coral reef ecosystems. Rev. Aquat. Sci. 1: 243–280

    Google Scholar 

  • Altschuler ZS, Schnepfe MM, Silber CC & Simon FO (1983) Sulfur diagenesis in everglades peat and origin of pyrite in coal. Science 221(4607): 221–227

    Google Scholar 

  • Andersen FØ & Kristensen E (1988) Oxygen microgradients in the rhizosphere of the mangroveAvicennia marina. Mar. Ecol. Prog. Ser. 44: 201–204

    Google Scholar 

  • Canfield DE (1989) Reactive iron in marine sediments. Geochim. Cosmochim. Acta 53: 619–632

    Google Scholar 

  • Canfield DE, Raiswell R & Bottrell S (1992) The reactivity of sedimentary iron minerals toward sulfide. Am. J. Sci. 292: 659–683

    Google Scholar 

  • Carlson PR, Yarbro LA, Zimmermann CF & Montgomery JR (1983) Pore water chemistry of an overwash mangrove island. Florida Sci. 46(3/4): 233–238

    Google Scholar 

  • Casagrande DJ, Siefert K, Berschinski C & Sutton N (1977) Sulfur in peat-forming systems of the Okefenokee Swamp and Florida Everglades: origins of sulfur in coal. Geochim. Cosmochim. Acta 41: 161–167

    Article  Google Scholar 

  • Cline JD (1969) Spectrophotometric determination of hydrogen-sulfide in natural waters. Limnol. Oceanogr. 14: 454–458

    Google Scholar 

  • Ferdelman TG, Church TM & Luther III GW (1991) Sulfur enrichment of humic substances in a Delaware salt marsh sediment core. Geochim. Cosmochim. Acta 55: 979–988

    Google Scholar 

  • Fossing H & Jørgensen BB (1989) Measurement of bacterial sulfate reduction in sediments: evaluation of a single-step chromium reduction method. Biogeochem. 8: 205–222

    Google Scholar 

  • Fossing H, Thamdrup B & Jørgensen BB (1992) Havbundens svovl-, jern- og mangankredsløb i . Danish Environmental Protection Agency. Publication No. 15. Copenhagen

  • Francois R (1987) The influence of humic substances on the geochemistry of iodine in nearshore and hemipelagic marine sediments. Geochim. Cosmochim. Acta 51: 2417–2427

    Google Scholar 

  • Gardner LR (1990) Similation of the diagenesis of carbon, sulfur, and dissolved oxygen in salt marsh sediments. Ecological Monographs 60: 91–111

    Google Scholar 

  • Giblin A (1988) Pyrite formation in marshes during early diagenesis. Geomicrobiol. J. 6: 77–97

    Google Scholar 

  • Giblin AE & Howarth RW (1984) Porewater evidence for a dynamic sedimentary iron cycle in salt marshes. Limnol. Oceanogr. 29(1): 47–63

    Google Scholar 

  • Hart MGR (1959) Sulphur oxidation in tidal mangrove soils of Sierra Leone. Plant and Soil 11(3): 215–236

    Google Scholar 

  • Higashi T & Shinagawa A (1985) Soils of a mangrove forest composed ofRhizophora mucronata andBruguiera gymnorrhiza from Ishigaki Island, Japan. Soil Sci. Plant Nutr. 31(3): 427–435

    Google Scholar 

  • Hines ME, Knolmeyer SL & Tugel JB (1989) Sulfate reduction and other sedimentary biogeochemistry in a northern New England salt marsh. Limnol. Oceanogr. 34(3): 578–590

    Google Scholar 

  • Hines ME, Bazylinski DA, Tugel JB & Lyons WB (1991) Anaerobic microbial biogeochemistry in sediments from two basins in the Gulf of Maine: evidence for iron and manganese reduction. Estuar. Coast. Shelf. Sci. 32: 313–324

    Google Scholar 

  • Howarth RW (1984) The ecological significance of sulfur in the energy dynamics of salt marsh and coastal marine sediments. Biogeochem. 1: 5–27

    Google Scholar 

  • Howarth RW & Giblin A (1983) Sulfate reduction in the salt marshes at Sapelo Island, Georgia. Limnol. Oceanogr. 28(1): 70–82

    Google Scholar 

  • Howarth RW, Giblin A, Gale J, Peterson BJ & Luther III GW (1983) Reduced sulfur compounds in the pore waters of a New England salt marsh. Environ. Biogeochem. Ecol. Bull. 35: 135–152

    Google Scholar 

  • Howarth RW & Jørgensen BB (1984) Formation of35S-labelled elemental sulfur and pyrite in coastal marine sediments (Limfjorden and Kysing Fjord, Denmark) during short-term35SO4 2− reduction measurements. Geochim. Cosmochim. Acta 48: 1807–1818

    Article  Google Scholar 

  • Howarth RW & Merkel S (1984) Pyrite formation and the measurement of sulfate reduction in salt marsh sediments. Limnol. Oceanogr. 29(3): 598–608

    Google Scholar 

  • Huettel M & Gust G (1992) Impact of bioroughness on interfacial solute exchange in permeable sediments. Mar. Ecol. Prog. Ser. 89: 253–267

    Google Scholar 

  • Jørgensen BB (1978) A comparison of methods for the quantification of bacterial sulfate reduction in coastal marine sediments. I. Measurements with radiotracer techniques. Geomicrobiol. J. 1: 11–27

    Google Scholar 

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

    Google Scholar 

  • Jørgensen BB, Bang M & Blackburn TH (1990) Anaerobic mineralization in marine sediments from the Baltic Sea-North Sea transition. Mar. Ecol. Prog. Ser. 59: 39–54

    Google Scholar 

  • King GM (1988) Patterns of sulfate reduction and the sulfur cycle in a South Carolina salt marsh. Limnol. Oceanogr. 33(3): 376–390

    Google Scholar 

  • Kohnen MEL, Sinninghe Damsté JS, Kock-Van Dalen AC, Ten Haven HL, Rullkötter J & De Leeuw JW (1990) Origin and diagenetic transformations of C25 and C30 highly branched isoprenoid sulphur compounds: further evidence for the formation of organically bound sulphur during early diagenesis. Goechim. Cosmochim. Acta 54: 3053–3063

    Google Scholar 

  • Kristensen E & Andersen FØ (1987) Determination of organic carbon in marine sediments: a comparison of two CHN-analyzer methods. J. Exp. Mar. Biol. Ecol. 109: 15–23

    Google Scholar 

  • Kristensen E, Holmer M, Bussarawit N (1991) Benthic metabolism and sulfate reduction in a southeast Asian mangrove swamp. Mar. Ecol. Prog. Ser 73: 93–103

    Google Scholar 

  • Kristensen E, Devol AH, Ahmed SI & Saleem M (1992) Preliminary study of benthic metabolism and sulfate reduction in a mangrove swamp of the Indus Delta, Pakistan. Mar. Ecol. Prog. Ser. 90: 287–297

    Google Scholar 

  • Kristensen E, King GM, Holmer M, Banta GT, Jensen MH & Hansen K (1994) Sulfate reduction, acetate turnover and carbon metabolism in sediments of the Ao Nam Bor Mangrove, Phuket, Thailand. Mar. Ecol. Prog. Ser. 109(2–3): 245–255

    Google Scholar 

  • Lord III CJ & Church TM (1983) The geochemistry of salt marshes: sedimentary ion diffusion, sulfate reduction, and pyritisation. Geochim Cosmochim. Acta 47: 1381–1391

    Google Scholar 

  • Lovley DR & Phillips EJP (1987) Rapid assay for microbially reducible ferric iron in aquatic sediments. Appl. Environ. Microbiol. 53: 2636–2641

    Google Scholar 

  • Luther III GW, Giblin AE & Varsolona RV (1985) Polarographic analysis of sulfur species in marine porewaters. Limnol. Oceanogr. 30(4): 727–736

    Google Scholar 

  • Luther III GW, Church TM, Scudlark JR & Cosman M (1986) Inorganic and organic sulfur cycling in salt-marsh pore waters. Science 232: 746–749

    Google Scholar 

  • Luther III GW, Ferdelman TG, Kostka JE, Tsamakis EJ & Church TM (1991) Temporal and spatial variability of reduced sulfur species (FeS2, S2O3 2−) and porewater parameters in salt marxh sediments. Biogeochem. 14: 57–88

    Google Scholar 

  • McKee KL, Mendelssohn IA & Hester MW (1988) Reexamination of pore water sulfide concentrations and redox potentials near the aerial roots ofRhizophora mangle andAvicennia germinans. Amer. J. Bot. 75(9): 1352–1359

    Google Scholar 

  • Mongia AD & Ganeshamurthy AN (1989) Typical differences between the chemical characteristics ofRhizophora andAvicennia mangrove forest soils in South Andamans. Agrochimica. 33(6): 464–470

    Google Scholar 

  • Moses CO & Herman JS (1991) Pyrite oxidation at circumneutral pH. Geochim. Cosmochim. Acta 55: 471–482

    Google Scholar 

  • Oenema O (1990) Pyrite accumulation in salt marshes in the Eastern Scheldt, southwest Netherlands. Biogeochem. 9: 75–98

    Google Scholar 

  • Rickard DT (1975) Kinetics and mechanism of pyrite formation at low temperatures. Am. J. Sci. 275: 636–652

    Google Scholar 

  • Silva CAR, Lacerda LD & Rezende CE (1990) Metals reservoir in a red mangrove forest. Biotropica 22(4): 339–345

    Google Scholar 

  • Skyring GW (1987) Sulfate reduction in coastal ecosystems. Geomicrobial. J. 5 (3/4): 295–374

    Google Scholar 

  • Stookey LL (1970) Ferrozine — a new spectrophotometric reagent for iron. Analyt. Chem. 42: 779–781

    Google Scholar 

  • Swider KT & Mackin JE (1989) Transformation of sulfur compounds in marsh-flat sediments. Geochim. Cosmochim. Acta 53: 2311–2323

    Google Scholar 

  • Sørensen J (1982) Reduction of ferric iron in anaerobic, marine sediment and interaction with reduction of nitrate and sulfate. Appl. Environ. Microbiol. 43: 319–324

    Google Scholar 

  • Thibodeau FR & Nickerson NH (1986) Differential oxidation of mangrove substrate byAvicennia germinans andRhizophora mangle. Amer. J. Bot. 73(4): 512–516

    Google Scholar 

  • Thode-Andersen S & Jørgensen BB (1989) Sulfate reduction and the formation of35S-labeled FeS, FeS2, and S° in coastal marine sediments. Limnol. Oceanogr. 34(5): 793–806

    Google Scholar 

  • Urban NR & Brezonik PL (1993) Transformation of sulfur in sediment microcosms. Can. J. Fish. Aquat. Sci. 50: 1946–1960

    Google Scholar 

  • Wallmann K, Hennies K, König I, Petersen W & Knauth H-D (1993) New procedure for determining reactive Fe(III) and Fe(II) minerals in sediments. Limnol. Oceanogr. 38(8): 1803–1812

    Google Scholar 

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Author notes

  1. Marianne Holmer

    Present address: Department of Life Sciences and Chemistry, 17.2, Roskilde University, P.O. Box 260, DK-4000, Roskilde, Denmark

Authors and Affiliations

  1. Institute of Biology, Odense University, Campusvej 55, DK-5230, Odense M, Denmark

    Marianne Holmer, Erik Kristensen, Gary Banta, Kim Hansen & Mikael Hjort Jensen

  2. Phuket Marine Biological Center, P.O. Box 60, Phuket, 83000, Thailand

    Nipuvan Bussawarit

Authors
  1. Marianne Holmer
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  2. Erik Kristensen
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  3. Gary Banta
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  4. Kim Hansen
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  5. Mikael Hjort Jensen
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  6. Nipuvan Bussawarit
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Holmer, M., Kristensen, E., Banta, G. et al. Biogeochemical cycling of sulfur and iron in sediments of a south-east Asian mangrove, Phuket Island, Thailand. Biogeochemistry 26, 145–161 (1994). https://doi.org/10.1007/BF00002904

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  • DOI: https://doi.org/10.1007/BF00002904

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