References
- Deep-Sea Res. v.42 Sulfate reduction rates and low molecular weight fatty acid concentrations in the water column and surficial dediments of the Black Sea. Albert, D.B.;C. Taylor;C.S. Martens https://doi.org/10.1016/0967-0637(95)00042-5
- J. Mar. Res. v.41 Comparative biogeochemistry of water in intertidal Onuphis (Polychaeta) and Upogebia (Crustacea) burrows: temporal patterns and causes. Aller, R.C.;J.Y. Yingst;W.J. Ullman https://doi.org/10.1357/002224083788519722
- Nitrogen cycling in coastal marine environments Benthic fauna and biogeochemical processes in marine sedimints: the role of burrow structures. Aller, R.C.;Blackburn, T.H.(ed);J. Sorensen(ed)
- J. Mar. Res. v.46 Microbial-meiofaunal interrelationships in some tropical intertidal sediments. Alongi, D.M. https://doi.org/10.1357/002224088785113630
- Coastal Ecosystem Processes Alongi, D.M.
- J. Exp. Mar. Biol. Ecol. v.225 The influence of stand age on binthic decomposition and recydling of organic matter in managed mangrove forests of Malaysia. Alongi, D.M.;A. Sasekumar;F. Tirindi;P. Dixon https://doi.org/10.1016/S0022-0981(97)00223-2
- Mar. Geol. v.179 Organic carbon accumulation and metabolic pathways in sediments of mangrove forests in southern thailand. Alongi, D.M.;G. Wattayakorn;J. Pfitzner;F. Tirendi;I. Zagorskis;G.J. Brunskill;A. Davidson;B.F. Clough https://doi.org/10.1016/S0025-3227(01)00195-5
- Limnol. Oceanogr. v.37 The impertance of benthic macrofauna in decomposition of microalgae in a coastal marine sediment. Andersen, F.O.;E. Kristensen https://doi.org/10.4319/lo.1992.37.7.1392
- Geomicrobiol. J. v.15 Study of biofilms of sulfidogens from North Sea oil production facilities using continuous-flow apparatus. Bass, C.;P. Sanders;H. Lappin-Scott https://doi.org/10.1080/01490459809378068
- Productivity of the ocean; present and past Ocean productivity and paleoproductivity-an overview. Berger, W.H.;V.S. Smetacet;G. Wefer;W.H.(ed); V.S. Smetacet(ed);G. Wefer(ed)
- Arch. Microbiol. v.121 The effects of temperature on the fatty acid and phospholipid composition of four obligately psychrophilic Vibrio spp. Bhakoo, M.;R.A. Herbert https://doi.org/10.1007/BF00689975
- Nitrogen cycling in coastal marine environments Modelling benthic nitrogen cycling in temperate coastal ecosystems. Billen, G.;C. Lancelot;Blackburn, T.H.(ed);J. Sorensen(ed)
- Aquat. Microb. Ecol. v.15 Diel cycles of sulphate redudtion rates in sediments of a Zostera marina bed(Dinmark). Blaabjerg, V.;K.N. Mouritsen;K. Finster https://doi.org/10.3354/ame015097
- Mar. Ecol. Prog. Ser. v.44 C- and N-miner-alization in the sedimints of earthen marine fishponds. Blackburn, T.H.;B.A. Lund;M. Krom https://doi.org/10.3354/meps044221
- Mar. Ecol. Prog. Ser. v.23 Nutrient regeneration and oxygen consumption by sedimints along an estuarine salinity gradient. Boynton, W.R.;W.M. Kemp https://doi.org/10.3354/meps023045
- J. Exp. Mar. Biol. Ecol. v.109 The effect of salmon on the benthos of a Scottish sea loch. Brown, J.R.;R.J. Gowen;D.S. McLusky https://doi.org/10.1016/0022-0981(87)90184-5
- Estuar. Coast. Shelf Sci. v.19 Deoxygenation and renineralization above the sediment-water interface; an in situ experimental study. Bulleid, N.C. https://doi.org/10.1016/0272-7714(84)90050-7
- Science v.251 Aerobic sulfate reduction in microbial mats. Canfield, D.E.;D.J. Des Marais https://doi.org/10.1126/science.11538266
- Interactions of C, N, P and S biogeochemical cysles and global change Organic matter oxidation in marine sediments. Canfield, D.E.;Wollast, R.(ed);F.T. Mackenzie(ed);L. Chou(ed)
- Chem. Geol. v.114 Factors influencing organic carbon preservation in marine sedimints. Canfield, D.E. https://doi.org/10.1016/0009-2541(94)90061-2
- Chem. Geol. v.54 The use of chromium reduction in the analysis of riduced inorganic sulfur in sedimints and shales. Canfield, D.E.;R. Raiswell;J.T. Westrich;C.M. Reaves;R.A. Berner https://doi.org/10.1016/0009-2541(86)90078-1
- Geochim. Cosmochin Acta v.57 The anaerobic degradation of organic matter in Danish coastal sediments: Iron reduction, manganese reduction, and sulfate reduction. Canfield, D.E.;B. Thamdrup;J.W. Hansen https://doi.org/10.1016/0016-7037(93)90340-3
- Mar. Geol. v.113 Pathways of roganic carbon oxidation in three continental margin sediments. Canfield, D.E.;B.B. Jorgensen;H. Fossing;R. Glud;J. Gundersen;N.B. Ramsing;B. Thamdrup;J.W. Hamsen;L.P. Nielsen;P.O.J. Hall https://doi.org/10.1016/0025-3227(93)90147-N
- Geochim. Cosmochim. Acta v.60 Reactivity of recently deposited organic matter. degradation of lipid compunds mear the sediment-water interface. Canuel, E.A.;C.S. Martens https://doi.org/10.1016/0016-7037(96)00045-2
- Limnol. Oceanogr. v.33 Comparison of microbial dynamics in marine and freshwater sediment: Contrasts in anaerobic carbon catabolism. Capone, D.G.;R. Kiene https://doi.org/10.4319/lo.1988.33.4_part_2.0725
- Appl. Environ. Microbiol. v.60 Emaymatic catalysis of mercury methylation by Desulfovibrio desulfuricans LS. Choi, S.C.;T. Chase, Jr;R. Bartha
- Aquat. Microb. Ecol. v.21 Sediment mineralization, nutrient fluxes, denitrification and dissimilatory nitrate reduction to ammonium in an estuarine fjord with sea cage trout farms. Christensen, P.B.;S. Rysgaard;N.P. Sloth;T. Dalsgaard;S. Schwarter https://doi.org/10.3354/ame021073
- Mar. Ecol. Prog. Ser. v.43 Bacterial production in fresh and saltwater ecosystems: a cross-system overview. Cole, J.J.;M.L. Pace;S. Findlay https://doi.org/10.3354/meps043001
- Ann. Rev. Microbiol. v.54 Oxygen respiration by Desulfovibrio species. Cypolnka, H. https://doi.org/10.1146/annurev.micro.54.1.827
- Mar. Ecol. Prog. Ser. v.215 Effect of oxygen on the degradabiltiy of organic matter in subtidal and intertidal sedimints of thd North Sea area. Dauwe, B.;J.J. Middelburg;P.M.J. Herman https://doi.org/10.3354/meps215013
- The Sulfate-reducing bacteria: contemporary Perspectives Phylogeny of sulfate-reducing bacteria and a perspective for analysing their natural communities. Devereux, R.;D.A. Stahl;Odom, J.M.(ed);R. Singleton, Jr.(ed)
- Adv. Microb. Ecol. v.12 Oceanic bacterial production. Ducklow, H.W.;C.A. Carlson https://doi.org/10.1007/978-1-4684-7609-5_3
- Sulfate-Reducing Bacteria Metabokism of environmental contaminations by mixed and pure cultures of sulfate-reducing bacteria. Ensley, B.D.;J.M. Suflita;Barton, L.L.(ed)
- Appl. Environ. Microbiol. v.58 Rates of microbenthic and meiobenthic baterivory in a temperate muddy flat community. Epstein, S.S.;M.P. Shiaris
- Sul-fate-Reducing Bacteria Ecology of sulfate-reducing bacteria Fauque, G.D.;Barton, L.L.(ed)
- Limnol. Oceanogr. v.44 Sulfate reduction in surface sedimints of the southeast Atlantic comtinental margin between 15 °28'S and 27 °57'S (Angola and Namibia). Ferdelman, F.G.;H. Fossing;K. Neumann;H.D. Schulz https://doi.org/10.4319/lo.1999.44.3.0650
- Biogeochem. v.8 Measurement of bacterial sulfate reduction in sediments: evaluation of a single chromium reduction method. Fossing, H.;B.B. Jorgensen
- Geochim. Cosmochim. Acta v.43 Early oxidation of organic matter in pelagic sediments of eastern equatorial Atlantic: suboxic diagenesis. Froelich. P.N.;G.P. Klinkgammer;M.L. Bender;N.A. Luedtke;G.R. Heath;D. Cullen;P. Dauphin;D. Hammond;B. Hartman;V. Maryland https://doi.org/10.1016/0016-7037(79)90095-4
- Appl. Environm. Microbiol. v.58 Diurnal of sulfate reduction under oxic conditions in cyanobacterial mats. Frund, C.;Y. Cohen
- J. Appl. Bacteriol. v.69 Physiology and ecology of the sulphate-reducing bacteria. Gibson, G.R. https://doi.org/10.1111/j.1365-2672.1990.tb01575.x
- Mar. Ecol. Prog. Ser. v.186 The importance of ciliates for interstitial transport in marine sediments. Glud, R.N.;T. Fenchel https://doi.org/10.3354/meps186087
- Mar. Ecol. Prog. Ser. v.206 Benthic carbon mineralization in a high-Arctic sound (Young Sound, NE Greenland). Glud, R.N.;N. Risgaard-Petersen;B. Thamdrup;H. Fossing;S. Rysgaard https://doi.org/10.3354/meps206059
- Bacterial motabolism. Gottschalk, G.
- Mar. Ecol. Prog. Ser. v.61 Chemical flrxes and mass balances in a marine fish cage farm. I. Carbon. Hall, P.O.J.;L.G. Anedrson;O. Holby;S. Kollberg;M.-O. Samuelsson https://doi.org/10.3354/meps061061
- Sulfate-Reducing Bacteria Biocorrosion Hamilton, W.A.;W. Lee;Barton, L.L.(ed)
- Aquat. Microb. Ecol. v.10 Imapact of the softxhell clam Mya arenaria on sulfate reduction in an intertidal sediment. Hansen, K.;G.M. King;E. Kristensen https://doi.org/10.3354/ame010181
- Mar. Ecol. Prog. Ser. v.75 Aerobic and anaerobic mineralization of ogranic material in marine sediment microcosms. Hansen, L.S.;T.H. Blackburn https://doi.org/10.3354/meps075283
- The Sulfate-reducing bacteria: contemporary Perspectives Cabon metabolisom of sulfate-reducing bacteria. Hansen, T.A.;Odom, J.M.(ed);R. Singleton, Jr.(ed)
- Geochim. Cosmochim. Acta v.59 Kinetics of phytoplankton decay during simulated sedimentation: Changes in biochemical composition and microbial activity under oxic and anoxic conditions. Harvey, H.R.;J.H. Tuttle;J.T. Bell https://doi.org/10.1016/0016-7037(95)00217-N
- Mar. Chem. v.49 Sedimentary organic matter preservation: an assessment and speculative synthesis. Hedges, J.I.;R.G. Keil https://doi.org/10.1016/0304-4203(95)00008-F
- Mar. Chem. v.39 Early diagenesis of organic matter in marine sediment. Henrichs, S.M. https://doi.org/10.1016/0304-4203(92)90098-U
- Estuar. Coast. Shelf Sci. v.20 Microbial biogeochemistry and bioturbation in the sediments of Great Bay, New Hampshire. Hines, M.E.;G.E. Jones https://doi.org/10.1016/0272-7714(85)90029-0
- Limnol. Oceanogr. v.34 Sulfate reduction and other sedimentary biogeochemistry in a northem New England salt marsh. Hines, M.E.;S.L. Knollmeyer;J.B. Tugel https://doi.org/10.4319/lo.1989.34.3.0578
- Estuar. Coast. Shelf Sci. v.32 Anaerobic microbial biogeochemistry in sediments fron two basins in the Gulf of Maine: evidence for iron and manganese reduction. Hines, M.E.;D.A. Bazylinski;J.B. Tugel;W.B. Lyons https://doi.org/10.1016/0272-7714(91)90046-E
- Limnol. Oceanogr. v.39 Acetate concentrations and oxidation in salt marsh sediments. Himes, M.E.;G.T. Banta;A.E. Giblin;J.E. Hobbie;J.B. Tugel https://doi.org/10.4319/lo.1994.39.1.0140
- Biogeochem. v.39 Sedimentary anaerobic microbial biogeochemistry in the Gulf of Trieste, northem Adriatic Sea: Influences of bottom water owygen depletion. Hines, M.E.;J. Faganeli;R. Planinc https://doi.org/10.1023/A:1005806508707
- App. Environm. Microbiol. v.65 Molecular phylogenetic and biogeochemical studies of sulfate-reducing bacteria in the rhizosphere of Spartina alterniflora. Hines, M.E.;R.S.Evans;B.R.S. Genthner;S.G. Willis;S. Friedman;J.N. Rooney-Varga;R.Devereux
- Mar. Ecol. Progr. Ser. v.80 Impact of marine fish cagefarming on metabolism and sulfate reduction of underlying sediments. Holmer, M.;E. Kristensen https://doi.org/10.3354/meps080191
- Biogeochem. v.32 Seasonality of sulfate reduction and pore water solutes in a marine fish farm sediment: the importance of temperature and sedimentary organic matter. Holmer, M.;E. Kristensen
- Aquat. Microb. Ecol. v.20 Transformation and exchange processes in the Bangrong mangrove forest-seagrass bed system, Thailand. Sea-sonal and spatial variations in benthic metabolism and sulfur bio-geochemistry. Holmer, M.;F.O. Andersen;N. Holmboe;E. Kristensen;N. Thongtham https://doi.org/10.3354/ame020203
- Aquat. Botany v.71 The importance of mineralization based on sulfate reduction for nutrient regeneration in tropical seagrass sediments. Holmer, M.;F.Ol Andersen;S.L. Nielsen;T.S. Boschker https://doi.org/10.1016/S0304-3770(01)00170-X
- Mar. Ecol. Prog. Ser. v.225 Effects of sea level rise on growth of Spartina anglica and oxygen dynamics in rhizosphere and salt marsh sediments. Holmer, M.;B. Gribsholt;E. Kristensen https://doi.org/10.3354/meps225197
- Aquatic microbiology: An ecological approach Microbial processes in salt-marsh sediments. Howarth, R.W.;Ford, T.E.(ed)
- Oecologia v.97 Oxygen loss from Spartina alterniflora and its relationship to salt marsh oxygen balance. Howes, B.L.;J.M. Teal https://doi.org/10.1007/BF00325879
- Microb. Ecol. v.33 The formation of large bacterial aggergates at depth within the Louisiana hydricarbon seep zone. Hyun, J.-H.;B.M. Bennison;P.A. LaRock https://doi.org/10.1007/s002489900024
- Bio-Science v.29 Chemosynthetic primary production at East Pacific sea floor spreading centers. Jannasch, H.W.;C.O. Wirsen
- Mar. Ecol. Prog. Ser. v.48 Denitrification in coastal bay sedimint: regional and seasonal variation in Aarhus Bight, Denmark. Jensen, M.H.;T.K. Andersen;J. Sorensen https://doi.org/10.3354/meps048155
- Limnol. Oceanogr. v.22 The sulfur cycle of a coastal marine sediment (Limfjorden, Denmark). Jorgensen, B.B. https://doi.org/10.4319/lo.1977.22.5.0814
- Nature v.296 Mineralization of roganic matter in the sea bed - the role of sulphate reduction. Jorgensen, B.B. https://doi.org/10.1038/296643a0
- Marine geochemisty Bacteria and marine biogeochemistry. Jorgensen, B.B.;Schulz, H.D.(ed);M. Zabel(ed)
-
Mar. Ecol. Prog. Ser.
v.24
Seasonal cycles of O₂,
$^NO₂{-}$ and$^SO₄{2-}$ reduction in estuarine sedimints: the significance of an NO₃$^{-}$ reduction maximum in spring. Jorgensen, B.B.;J. Sorensin https://doi.org/10.3354/meps024065 - Deep-Sea Res. v.37 Thermophilic bacterial sulfate reduction in deep-sea sediments at the Guaymas basin hydrotherma vent site (Gulf of California)ll Jorgensen, B.B.;L.X. Zawacki;H.W. Jannasch https://doi.org/10.1016/0198-0149(90)90099-H
- J. Kor. Soc. Oceanogr. v.7 A study of the macrozoobenthos at the intensive fish farming grounds in the southem coast of Korea,[The Sea] Jung, R.-H.;H.-S Lim;S.-S. Kim;J.-S. Park;K.-A. Jeon;Y.-S. Lee;J.-S. Lee;K.-Y. Kim;W.-J. Go
- Science. v.207 Deep-sea primary production at the Galapagos hydrothetmal vents. Karl, D.M.;C.O. Eirsen;H.W. Jannasch https://doi.org/10.1126/science.207.4437.1345
- Appl. Environ. Microbiol. v.66 Sulfate-reducing bacteria methylate mercury at variable rates in pure culture and in marine sediments. King, J.K.;J.E. Kostka;M.E. Frischer;F.M. Saunder https://doi.org/10.1128/AEM.66.6.2430-2437.2000
- Nature v.233 Corrosion by sulfate-reducing bacteria. King, R.A.;J.D.A. Miller https://doi.org/10.1038/233491a0
- FEMS Microbiol. Ecol. v.73 Effects of added manganic and ferric oxides on sulfate reduction and sulfide oxidation in intertidal sediments. King. G.M. https://doi.org/10.1111/j.1574-6968.1990.tb03933.x
- Appl. Environ. Microbiol. v.65 Community size and metabolic rates of psychrophilic sulfate-reducing bacteria in Arctic marine sediments. Knoblauch, C.;B.B. Jorgensen;J. Harder
- Mar. Ecol. Ser. v.180 Rates and pathways of carbon oxidation in permanently cold Arctic sedimints. Kostka, J.E.;B. Thamdrup;R.N. Glud;D.E. Canfield https://doi.org/10.3354/meps180007
- Biogeochem. v.60 Rates and controls of anaerobic microbial respiration across spatial and temporal gradients in saltmarsh sedimints. Kostka, J.E.;A. Roychoudhury;P. Van Cappellen https://doi.org/10.1023/A:1016525216426
- Limnol. Oceanogr. v.47 The rates and pathways of carbon oxidation in bioturbated saltmarsh sediments. Kostka, J.E.;B. Gribsholt;E. Petrie;D. Dalton;H. Skelton;E. Kristensen https://doi.org/10.4319/lo.2002.47.1.0230
- Mar. Ecol. Prog. Ser. v.90 Preliminary study of benthic metabolism and sulfate reduction in a mangrove swamp of the Indus Dolta, Pakistan. Kristensen, E.;A.H. Devol;S.I. Ahmed;S. Monawwar https://doi.org/10.3354/meps090287
- Mar. Ecol. Prog. Ser. v.109 Acetate turnover, sulfate reduction and carbon metabolism in sediments of the Ao Nam Bor mantrove, Phuket, Thailand. Kristensen, E.;G.M. King;G.T. Banta;M. Holmer;M.H. Jensen;K. Hansen;N. Bussarawit https://doi.org/10.3354/meps109245
- Limnol. Oceanogr. v.40 Aerbic and anaerobic decomposition of organic matter in marine sediment: Which is fast? Kristensen, E.;A.I. Ahmed;A. Devol https://doi.org/10.4319/lo.1995.40.8.1430
- Aquat. Microb. Ecol. v.22 Carbon and nitrogen mineralization in sedimints of the Bangrong mangrove area, Phuket, Thailand. Kristensen, E.;F.O. Andersen;N. Holmboe;M. Holmer;N. Thongtham https://doi.org/10.3354/ame022199
-
Geochim. Cosmochim. Acta
v.65
Decomposition of plant materials in marine sediment exposed to different electron acceptors (O₂,
$NO₃^{-}$ ,and$SO₄^{2-}$ , with emphasis on substrate origin, degradation kinetics, and the role of bioturbation. Kristensen, E.;M. Holmer https://doi.org/10.1016/S0016-7037(00)00532-9 - Mar. Ecol. Prog. Ser. v.5 Energy flow in a tidal flat ecosystem. Kuipers, B.R.;P.A.W.J.de Eilde;F. Creutzberg https://doi.org/10.3354/meps005215
- Geo. Mar. Lett. v.14 Bacterioplankton growth and production at the Louisiana hydrocarbon seeps. LaRock, P.A.;J.-H. Hyun;B.W. Bennison https://doi.org/10.1007/BF01203721
- Appl. Environ. Microbiol. v.61 Application of antisera raised against sulfate reducing bacteria for inderect immunofluorescent detection of immunoreactive bacteria in sediment from the German Baltic Sea. Lillebak, R.
- J. Kor. Soc. Oceanogr. v.7 The outbreak, maintenance, and decline of the red tide dominated by Cochlodinium ploykrikoides in the coastal waters off southerm Korea from August to October, 2000. [The Sea], Lim, W.-A.;C.-S. Jung;C,-K. Lee;Y.-C. Cho;S.-G. Lee;H.-G. Kim;I.-K. Chung
- Microbiol. Rev. v.55 Dissimilatory Fe(Ⅲ) and Mn(Ⅳ) reduction. Lovley, D.R.
- Appl. Environ. Microbiol. v.53 Competitive mechanisms for ingibition of sulfate reduction and methane production in the zone of ferric iron erduction in sediments. Lovley, D.R.;E.J.P. Phillips
- Geonicrobiol. J. v.6 Manganese inghbition of microbial iron erduction in anaerobic sediments. Lovley, D.R.;E.J.P. Phillips https://doi.org/10.1080/01490458809377834
- Appl. Environ. Microbiol. v.54 Novel mode of microbial energy metabolism: organic carbon oxidation coupled to dissimilatory reduction of iron and manganese. Lovley, D.R.;E.J.P. Phillips
- J. Mar. Res. v.47 Organic matter decomposition pathways and oxygen consumption in coastal marine sediments. Mackin, J.E.;K.T. Swider https://doi.org/10.1357/002224089785076154
- Appl. Geochem. v.5 Generation of short chain organic acid anion in hydrothrmally altered sediments of the Guaymas basin, Gulf of California. Martens, C.S. https://doi.org/10.1016/0883-2927(90)90037-6
- Science v.185 Methane production in the interstitial waters of sulfate depleted marine sediments. Martens, C.S.;R.A. Berner https://doi.org/10.1126/science.185.4157.1167
- Biogeochem. v.27 Sulfur and iron cycling in a coastal sediment: radiotracer studies and sea-sonal dynamics. Moeslund, L.;B. Thamdrup;B.B. Jorgensen
- Mar. Ecol. Prog. Ser. v.27 Gas advection in sediments of a South Carolina salt marsh. Morris, J.T.;G.J. Whiting https://doi.org/10.3354/meps027187
- Geochim. Cosmochim. Acta v.52 Microbial reduction of mangenese oxides: interactions with iron and sulfur. Meyers, C.;K.H. Mealson https://doi.org/10.1016/0016-7037(88)90041-5
- Mar. Ecol. Prog. Ser. v.119 Estuarine nitrogen retention independently estimated by the denitrification rate and mass balance methods: a study of Norsminde Fjord, Denmark. Nielsen, K.;L.P. Nielsen;P. Rasmussen https://doi.org/10.3354/meps119275
- Ophelia v.41 Coastal marine eutrophication: a definition, social causes, and future concerns. Nixon, S.W.
- Appl. Environ. Microbiol. v.65 Analyses of spatial distributions of sulfate-reducing bacteria and their activity in aerobic wastewater biofilms. Okabe, S.;T. Itoh;H. Satoh;Y. Watanabe
- Appl. Environ. Microbiol. v.44 Methanogenesis and sulphate reduction: competitive and non-competitive substrates in estuarine sediments. Oremland, R.S.;S. Polcin
- The ecolgy of saltnarsh. Pomeroy, L.R.;R.G. Wiegert
- Mar. Ecol. Prog. Ser. v.44 Impact of bioturbation by Arenicola marina on microbiological parameters in intertidal sediments Reichardt, W. https://doi.org/10.3354/meps044149
- Limnol. Oceanogr. v.31 Oxygen production and consumption in sediments determined at high spatial tesolution by computer simulation of oxygen microelectrode data. Revsbech, N.P.;B. Madsen;B.B. Jorgensen https://doi.org/10.4319/lo.1986.31.2.0293
- Aqust. Microb. Ecol. v.21 Marine meiofauna, carbon and netrogen mineralization in sandy and soft sediments of Disko Bay, west Greenland. Rysgaard, S.;P.B. Christensen;M.V. Sorensen;P. Funch;P. Berg https://doi.org/10.3354/ame021059
- Geomicrobiol. J. v.15 Temperature dependence and sulfate reduction in cold sediments of Svalbard Arctic Ocean. Sagemann, J.;B.B. Jorgensen;O. Greeff https://doi.org/10.1080/01490459809378067
- Limnol. Oceanogr. v.29 Above-and bilowground energent macrophyte production and tumover in a coastal marsh ecosystiem, Georgia. Schubauer, J.P.;C.S. Hopkinson https://doi.org/10.4319/lo.1984.29.5.1052
- The sulfate-reducing bactera: contemporaty perspectives The sulfate-reducing bacteria: an overview. Singleton, Jr. R.
- Geochim. Cosmochim. Acta. v.51 Early diagenesis in sediments from Danish coastal waters: microbial activity and Mn-Fe-S geocheistry. Sorensen, J.;B.B. Jorgensen https://doi.org/10.1016/0016-7037(87)90339-5
- The microbial world. 5th ed. Stainer, R.Y.;E.A. Adelberg;J. Ingragam
- Adv. Microb. Ecol. v.16 Bacterial manganese and iron reduction in aquatic sediments. Thamdrup, B. https://doi.org/10.1007/978-1-4615-4187-5_2
- Limnol. Oceanogr. v.41 Pathways of carbon oxidation in continental margin sediments off central Chile. Thamdrup, B.;D.E. Canfield https://doi.org/10.4319/lo.1996.41.8.1629
- Methods in ecosystim science Benthic respiration in aquatic sediments. Thamdrup, B.;D.E. Canfield;Jackson, R.B.(ed);O.E. Sala;H.A. Mooney;R.W. Howarth(ed)
- Geochim. Cosmochim. Acta v.58 Manganese, iron, and sulfur cycling in a coastal marine sediment, Asrhaus Bay, Denmark. Thamdrup, B.;H. Fossing;B.B. Jorgensen https://doi.org/10.1016/0016-7037(94)90298-4
- Appl. Environ. Microbiol. v.66 Microbial manganese and sulfate reduction in Black Sea shelf secimints. Thamdrup, B.;R. Tossello-Mora;R. Amann https://doi.org/10.1128/AEM.66.7.2888-2897.2000
- Limnol. Oceanogr. v.29 The role of sedimintary organic matter in bacterial sulfate reduction: the G model tested. Westrich, J.T.;R.A. Berner https://doi.org/10.4319/lo.1984.29.2.0236
- The prokaryotes , 2nd. ed. v.4 Gram-negative mesophilic sulfatereducing bacteria. Widdel, F.;F. Bak;Balows, H.G.T.A.(ed);M. Dworkin(ed);W. Harder(ed);K.-H. Schleifer
- J. Exp. Mar. Biol. Ecol. v.145 Tracing the influence on sediments of organic waste from a salmonid farm using stable isotope analysis. Ye, L.-X.;D.A. Ritz;G.E. Fenton;M.E. Lewis https://doi.org/10.1016/0022-0981(91)90173-T