Changes in Organic Matter Biodegradability Influencing Sulfate Reduction in an Aquifer Contaminated by Landfill Leachate

Microbial Ecology - Tập 51 - Trang 535-542 - 2006
Steve H. Harris1, Jonathan D. Istok2, Joseph M. Suflita1
1Department of Botany and Microbiology, Institute for Energy and the Environment, University of Oklahoma, Norman, USA
2Department of Civil, Construction, and Environmental Engineering, Oregon State University, Corvallis, USA

Tóm tắt

In situ experiments were conducted to measure sulfate reduction rates and identify rate-limiting factors in a shallow, alluvial aquifer contaminated with municipal landfill leachate. Single-well, push–pull tests conducted in a well adjacent to the landfill with >8 mM dissolved organic carbon (DOC) exhibited a sulfate reduction rate of 3.2 μmol SO4 −2 (L sediment)−1 day−1, a value in close agreement with laboratory-derived estimates. Identical tests conducted in wells located 90 m downgradient where DOC levels remained high (>3 mM) showed no detectable sulfate consumption, and laboratory assays confirmed this observation. However, the rates of sulfate reduction in sediment samples obtained from this site were three times larger when they were amended with filter-sterilized groundwater from the upgradient location. The effect of various amendments on sulfate reduction rates was further examined in laboratory incubations using sediment collected from the downgradient site amended with 35S sulfate. Unamended sediments showed only weak conversion of the tracer to 35S sulfide (5 to 7 cpm/cm2), whereas the addition of Desulfovibrio cells increased 35S sulfide production to 44 cpm/cm2. However, the application of heat-killed Desulfovibrio had a similar stimulatory effect, as did a lactate amendment. Collectively, these findings indicate that the lack of measurable sulfate reduction at the downgradient site was not due to the absence of the necessary metabolic potential, the presence of lower sulfate concentration, or the quantity of electron donor, but by its biodegradability. The findings also indicate that field bioaugmentation attempts should be interpreted with caution.

Tài liệu tham khảo

Aeckersberg, F (1998) Growth, natural relationships, cellular fatty acids and metabolic adaptation of sulfate-reducing bacteria that utilize long-chain alkanes under anoxic conditions. Arch Microbiol 170: 361–369 Amirbahman, A, Schönenberger, R, Johnson, CA, Sigg, L (1998) Aqueous- and solid-phase biogeochemistry of a calcareous aquifer system downgradient from a municipal solid waste landfill (Winterthur, Switzerland). Environ Sci Technol 32: 1933–1940 Beeman, RE, Suflita, JM (1987) Microbial ecology of a shallow unconfined ground water aquifer polluted by municipal landfill leachate. Microb Ecol 14: 39–54 Bjerg, PL, Rügge, K, Pedersen, JK, Christensen, TH (1995) Distribution of redox-sensitive groundwater quality parameters downgradient of a landfill (Grindsted, Denmark). Environ Sci Technol 29: 1387–1394 van Breukelen, BM, Röling, WFM, Groen, J, Griffioen, J, van Verseveld, HW (2003) Biogeochemistry and isotope geochemistry of a landfill leachate plume. J Contam Hydrol 65: 245–268 Chapelle, FH, Bradley, PM (1997) Alteration of aquifer geochemistry by microorganisms. In: Hurst, CJ, Knudsen, GR, McInerney, MJ, Stetzenbach, LD, Walter, MV (Eds.) Manual of Environmental Microbiology, Chapter 61. ASM Press, Washington, DC, pp 558–564 Christenson, S, Scholl, MA, Schlottmann, JL, Becker, CJ (1999) Ground-water and surface-water hydrology of the Norman landfill research site. U.S. Geological Survey Water Resources Investigations Report 99-4018C. U.S. Geological Survey, West Trenton, NJ, pp 501–507 Cozzarelli, IM, Suflita, JM, Ulrich, GA, Harris, SH, Scholl, MA, Schlottmann, JL, Christenson, S (2000) Geochemical and microbiological methods for evaluating anaerobic processes in an aquifer contaminated by landfill leachate. Environ Sci Technol 34: 4025–4033 ElFantroussi, S, Belkacemi, M, Top, EM, Mahillon, J, Naveau, H, Agathos, SN (1999) Bioaugmentation of a soil bioreactor designed for pilot-scale anaerobic bioremediation studies. Environ Sci Technol 33: 2992–3001 Ensley, BD, Suflita, JM (1995) Metabolism of environmental contaminants by mixed and pure cultures of sulfate-reducing bacteria. In: Barton, LL (Ed.) Sulfate-Reducing Bacteria. Plenum Press, New York, pp 293–332 Fauque, GD (1995) Ecology of sulfate-reducing bacteria. In: Barton, LL (Ed.) Sulfate-Reducing Bacteria. Plenum Press, New York, pp 217–241 Harris, SH, Ulrich, GA, Suflita, JM (1999) Dominant terminal electron accepting processes occurring at a landfill leachate plume-impacted site as indicated by field and laboratory measurements. U.S. Geological Survey Water Resources Investigations Report 99-4018C. U.S. Geological Survey, West Trenton, NJ, pp 541–548 Istok, JD, Humphrey, MD, Schroth, MH, Hyman, MR, O'Reilly, KT (1997) Single-well “push–pull” tests for in situ determination of microbial activities. Groundwater 35: 619–631 Jakobsen, R, Postma, D (1994) In situ rates of sulfate reduction in an aquifer (Rømø, Denmark) and implications for the reactivity of organic matter. Geology 22: 1103–1106 Jørgensen, BB (1982) Mineralization of organic matter in the sea bed—the role of sulphate reduction. Nature 296: 643–645 Kleikemper, J, Pelz, O, Schroth, MH, Zeyer, J (2002) Sulfate-reducing bacterial community response to carbon source amendments in contaminated aquifer microcosms. FEMS Microbiol Ecol 42: 109–118 Krumholz, LR, McKinley, JP, Ulrich, GA, Suflita, JM (1997) Confined subsurface microbial communities in Cretaceous rock. Nature 386: 64–66 Kuever, J, Kulmer, J, Jannsen, S, Fischer, U, Blotevogel, K (1993) Isolation and characterization of a new spore-forming sulfate-reducing bacterium growing by complete oxidation of catechol. Arch Microbiol 159: 282–288 Lovley, DR, Klug, MJ (1985) Model for the distribution of sulfate reduction and methanogenesis in freshwater sediments. Geochchim Cosmochim Acta 50: 11–18 Lovley, 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 Ludvigsen, L, Albrechtsen, H-J, Heron, G, Bjerg, PL, Christensen, TH (1998) Anaerobic microbial redox processes in a landfill leachate contaminated aquifer (Grindsted, Denmark). J Contam Hydrol 33: 273–291 Ludvigsen, L, Albrechtsen, H-J, Ringelberg, DB, Ekelund, F, Christensen, TH (1999) Distribution and composition of microbial populations in a landfill leachate contaminated aquifer (Grindsted, Denmark). Microb Ecol 37: 197–207 McMahon, PB, Chapelle, FH (1991) Microbial production of organic acids in aquitard sediments and its role in aquifer geochemistry. Nature 349: 233–235 Nanny, MA, Ratusuk, N (2002) Characterization and comparison of hydrophic neutral and hydrophobic acid dissolved organic carbon isolated from three municipal landfill leachates. Water Res 36: 1572–1584 Newcombe, DA, Crowley, DE (1999) Bioremediation of atrazine-contaminated soil by repeated application of atrazine-degrading bacteria. Appl Microbiol Biotechnol 51: 877–882 Parkin, TB (1990) Characterizing the variability of soil denitrification (FEMS Symp 56). In Denitrification in Soil and Sediment, Plenum, New York, pp 213–228 Rügge, K, Bjerg, PL, Christensen, TH (1995) Distribution of organic compounds from municipal solid waste in the groundwater downgradient of a landfill (Grindsted, Denmark). Environ Sci Technol 29: 1395–1400 So, CM, Young, LY (1999) Isolation and characterization of a sulfate-reducing bacterium that anaerobically degrades alkanes. Appl Environ Microbiol 65: 2969–2976 Ulrich, GA, Breit, GN, Cozzarelli, IM, Suflita, JM (2003) Sources of sulfate supporting anaerobic metabolism in a contaminated aquifer. Environ Sci Technol 37: 1093–1099 Wagner-Döbler, I (2003) Microbial inoculants—snake oil or panacea? In: Head, IM, Singleton, I, Milner, MG (Eds.) Bioremediation: A Critical Review, Chapter 10. Horizon Scientific Press, Norfolk, England, pp 259–289 Weiner, JM, Lovley, DR (1998) Anaerobic benzene degradation in petroleum-contaminated aquifer sediments after inoculation with a benzene-oxidizing enrichment. Appl Environ Microbiol 64: 775–778 Winfrey, MR, Zeikus, JG (1977) Effect of sulfate on carbon and energy flow during microbial methanogenesis in freshwater sediments. Appl Environ Microbiol 33: 275–281 Zhang, X, Young, LY (1997) Carboxylation as an initial reaction in the anaerobic metabolism of naphthalene and phenanthrene by sulfidogenic consortia. Appl Environ Microbiol 63: 4759–4764