Articles | Volume 5, issue 6
https://doi.org/10.5194/bg-5-1587-2008
© Author(s) 2008. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/bg-5-1587-2008
© Author(s) 2008. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Constraints on mechanisms and rates of anaerobic oxidation of methane by microbial consortia: process-based modeling of ANME-2 archaea and sulfate reducing bacteria interactions
B. Orcutt
Department of Marine Sciences, University of Georgia, Athens, GA 30 602, USA
Marine Environmental Biology Section, University of Southern California, Los Angeles, CA 90 089, USA
C. Meile
Department of Marine Sciences, University of Georgia, Athens, GA 30 602, USA
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36 citations as recorded by crossref.
- Simultaneous enrichment of denitrifying methanotrophs and anammox bacteria Z. Ding et al. https://doi.org/10.1007/s00253-014-5936-8
- Single cell activity reveals direct electron transfer in methanotrophic consortia S. McGlynn et al. https://doi.org/10.1038/nature15512
- Engineering Cooperation in an Anaerobic Coculture A. Kane et al. https://doi.org/10.1128/AEM.02852-20
- Anaerobic oxidation of methane: an “active” microbial process M. Cui et al. https://doi.org/10.1002/mbo3.232
- Dynamic modeling of anaerobic methane oxidation coupled to sulfate reduction: role of elemental sulfur as intermediate A. Hatzikioseyian et al. https://doi.org/10.1007/s00449-020-02495-2
- Reverse Methanogenesis and Respiration in Methanotrophic Archaea P. Timmers et al. https://doi.org/10.1155/2017/1654237
- Lipid biomarker patterns reflect different formation environments of mussel- and tubeworm-dominated seep carbonates from the Gulf of Mexico (Atwater Valley and Green Canyon) H. Guan et al. https://doi.org/10.1016/j.chemgeo.2018.12.005
- Chemical inhibitors of methanogenesis and putative applications H. Liu et al. https://doi.org/10.1007/s00253-010-3066-5
- Direct Exchange of Electrons Within Aggregates of an Evolved Syntrophic Coculture of Anaerobic Bacteria Z. Summers et al. https://doi.org/10.1126/science.1196526
- Microbial interactions in the anaerobic oxidation of methane: model simulations constrained by process rates and activity patterns X. He et al. https://doi.org/10.1111/1462-2920.14507
- The Ongoing Mystery of Sea-Floor Methane M. Alperin & T. Hoehler https://doi.org/10.1126/science.1189966
- Microbial community structures of methane hydrate-bearing sediments in the Ulleung Basin, East Sea of Korea J. Lee et al. https://doi.org/10.1016/j.marpetgeo.2013.06.002
- Reach out and touch someone: potential impact of DIET (direct interspecies energy transfer) on anaerobic biogeochemistry, bioremediation, and bioenergy D. Lovley https://doi.org/10.1007/s11157-011-9236-9
- Distributions and carbon isotopic compositions of lipid biomarkers in authigenic carbonate crusts from the Nordic margin (Norwegian Sea) N. Chevalier et al. https://doi.org/10.1016/j.orggeochem.2010.03.012
- Spatial distribution of nitrogen fixation in methane seep sediment and the role of the ANME archaea A. Dekas et al. https://doi.org/10.1111/1462-2920.12247
- Anaerobic oxidation of methane in hypersaline cold seep sediments L. Maignien et al. https://doi.org/10.1111/j.1574-6941.2012.01466.x
- Anaerobic Oxidation of Methane: Progress with an Unknown Process K. Knittel & A. Boetius https://doi.org/10.1146/annurev.micro.61.080706.093130
- Subgroup Characteristics of Marine Methane-Oxidizing ANME-2 Archaea and Their Syntrophic Partners as Revealed by Integrated Multimodal Analytical Microscopy S. McGlynn et al. https://doi.org/10.1128/AEM.00399-18
- Zero-valent sulphur is a key intermediate in marine methane oxidation J. Milucka et al. https://doi.org/10.1038/nature11656
- Microbial Controls on the Biogeochemical Dynamics in the Subsurface M. Thullner & P. Regnier https://doi.org/10.2138/rmg.2019.85.9
- Anaerobic oxidation of methane driven by different electron acceptors: A review Y. Zhao et al. https://doi.org/10.1016/j.scitotenv.2024.174287
- Controls on Interspecies Electron Transport and Size Limitation of Anaerobically Methane-Oxidizing Microbial Consortia X. He et al. https://doi.org/10.1128/mBio.03620-20
- Novel Insights into the Distribution of Reduced Sulfur Species in Prairie Pothole Wetland Pore Waters Provided by Bismuth Film Electrodes B. McAdams et al. https://doi.org/10.1021/acs.estlett.6b00020
- Potential for Direct Interspecies Electron Transfer in Methanogenic Wastewater Digester Aggregates M. Morita et al. https://doi.org/10.1128/mBio.00159-11
- Optimizing the hybridization chain reaction-fluorescence in situ hybridization (HCR-FISH) protocol for detection of microbes in sediments Z. Jia et al. https://doi.org/10.1007/s42995-021-00098-8
- Assessing the Spatial and Temporal Variability of Diffusive Methane and Nitrous Oxide Emissions from Subtropical Freshwater Reservoirs R. Musenze et al. https://doi.org/10.1021/es505324h
- Methane dynamics in subtropical freshwater reservoirs and the mediating microbial communities R. Musenze et al. https://doi.org/10.1007/s10533-016-0206-8
- Carbon and sulfur back flux during anaerobic microbial oxidation of methane and coupled sulfate reduction T. Holler et al. https://doi.org/10.1073/pnas.1106032108
- Lipid biomarker patterns of authigenic carbonates reveal fluid composition and seepage intensity at Haima cold seeps, South China Sea H. Guan et al. https://doi.org/10.1016/j.jseaes.2018.04.035
- Methane leakage through the sulfate–methane transition zone of the Baltic seabed L. Lapham et al. https://doi.org/10.1038/s41561-024-01594-z
- Artificial electron acceptors decouple archaeal methane oxidation from sulfate reduction S. Scheller et al. https://doi.org/10.1126/science.aad7154
- Physiological Differentiation within a Single-Species Biofilm Fueled by Serpentinization W. Brazelton et al. https://doi.org/10.1128/mBio.00127-11
- Quantitative analysis of anaerobic oxidation of methane (AOM) in marine sediments: A modeling perspective P. Regnier et al. https://doi.org/10.1016/j.earscirev.2011.01.002
- Methane oxidation by anaerobic archaea for conversion to liquid fuels T. Mueller et al. https://doi.org/10.1007/s10295-014-1548-7
- Microbial Ecology of the Dark Ocean above, at, and below the Seafloor B. Orcutt et al. https://doi.org/10.1128/MMBR.00039-10
- Microbial methane cycling in a terrestrial mud volcano in eastern Taiwan Y. Chang et al. https://doi.org/10.1111/j.1462-2920.2011.02658.x
36 citations as recorded by crossref.
- Simultaneous enrichment of denitrifying methanotrophs and anammox bacteria Z. Ding et al. https://doi.org/10.1007/s00253-014-5936-8
- Single cell activity reveals direct electron transfer in methanotrophic consortia S. McGlynn et al. https://doi.org/10.1038/nature15512
- Engineering Cooperation in an Anaerobic Coculture A. Kane et al. https://doi.org/10.1128/AEM.02852-20
- Anaerobic oxidation of methane: an “active” microbial process M. Cui et al. https://doi.org/10.1002/mbo3.232
- Dynamic modeling of anaerobic methane oxidation coupled to sulfate reduction: role of elemental sulfur as intermediate A. Hatzikioseyian et al. https://doi.org/10.1007/s00449-020-02495-2
- Reverse Methanogenesis and Respiration in Methanotrophic Archaea P. Timmers et al. https://doi.org/10.1155/2017/1654237
- Lipid biomarker patterns reflect different formation environments of mussel- and tubeworm-dominated seep carbonates from the Gulf of Mexico (Atwater Valley and Green Canyon) H. Guan et al. https://doi.org/10.1016/j.chemgeo.2018.12.005
- Chemical inhibitors of methanogenesis and putative applications H. Liu et al. https://doi.org/10.1007/s00253-010-3066-5
- Direct Exchange of Electrons Within Aggregates of an Evolved Syntrophic Coculture of Anaerobic Bacteria Z. Summers et al. https://doi.org/10.1126/science.1196526
- Microbial interactions in the anaerobic oxidation of methane: model simulations constrained by process rates and activity patterns X. He et al. https://doi.org/10.1111/1462-2920.14507
- The Ongoing Mystery of Sea-Floor Methane M. Alperin & T. Hoehler https://doi.org/10.1126/science.1189966
- Microbial community structures of methane hydrate-bearing sediments in the Ulleung Basin, East Sea of Korea J. Lee et al. https://doi.org/10.1016/j.marpetgeo.2013.06.002
- Reach out and touch someone: potential impact of DIET (direct interspecies energy transfer) on anaerobic biogeochemistry, bioremediation, and bioenergy D. Lovley https://doi.org/10.1007/s11157-011-9236-9
- Distributions and carbon isotopic compositions of lipid biomarkers in authigenic carbonate crusts from the Nordic margin (Norwegian Sea) N. Chevalier et al. https://doi.org/10.1016/j.orggeochem.2010.03.012
- Spatial distribution of nitrogen fixation in methane seep sediment and the role of the ANME archaea A. Dekas et al. https://doi.org/10.1111/1462-2920.12247
- Anaerobic oxidation of methane in hypersaline cold seep sediments L. Maignien et al. https://doi.org/10.1111/j.1574-6941.2012.01466.x
- Anaerobic Oxidation of Methane: Progress with an Unknown Process K. Knittel & A. Boetius https://doi.org/10.1146/annurev.micro.61.080706.093130
- Subgroup Characteristics of Marine Methane-Oxidizing ANME-2 Archaea and Their Syntrophic Partners as Revealed by Integrated Multimodal Analytical Microscopy S. McGlynn et al. https://doi.org/10.1128/AEM.00399-18
- Zero-valent sulphur is a key intermediate in marine methane oxidation J. Milucka et al. https://doi.org/10.1038/nature11656
- Microbial Controls on the Biogeochemical Dynamics in the Subsurface M. Thullner & P. Regnier https://doi.org/10.2138/rmg.2019.85.9
- Anaerobic oxidation of methane driven by different electron acceptors: A review Y. Zhao et al. https://doi.org/10.1016/j.scitotenv.2024.174287
- Controls on Interspecies Electron Transport and Size Limitation of Anaerobically Methane-Oxidizing Microbial Consortia X. He et al. https://doi.org/10.1128/mBio.03620-20
- Novel Insights into the Distribution of Reduced Sulfur Species in Prairie Pothole Wetland Pore Waters Provided by Bismuth Film Electrodes B. McAdams et al. https://doi.org/10.1021/acs.estlett.6b00020
- Potential for Direct Interspecies Electron Transfer in Methanogenic Wastewater Digester Aggregates M. Morita et al. https://doi.org/10.1128/mBio.00159-11
- Optimizing the hybridization chain reaction-fluorescence in situ hybridization (HCR-FISH) protocol for detection of microbes in sediments Z. Jia et al. https://doi.org/10.1007/s42995-021-00098-8
- Assessing the Spatial and Temporal Variability of Diffusive Methane and Nitrous Oxide Emissions from Subtropical Freshwater Reservoirs R. Musenze et al. https://doi.org/10.1021/es505324h
- Methane dynamics in subtropical freshwater reservoirs and the mediating microbial communities R. Musenze et al. https://doi.org/10.1007/s10533-016-0206-8
- Carbon and sulfur back flux during anaerobic microbial oxidation of methane and coupled sulfate reduction T. Holler et al. https://doi.org/10.1073/pnas.1106032108
- Lipid biomarker patterns of authigenic carbonates reveal fluid composition and seepage intensity at Haima cold seeps, South China Sea H. Guan et al. https://doi.org/10.1016/j.jseaes.2018.04.035
- Methane leakage through the sulfate–methane transition zone of the Baltic seabed L. Lapham et al. https://doi.org/10.1038/s41561-024-01594-z
- Artificial electron acceptors decouple archaeal methane oxidation from sulfate reduction S. Scheller et al. https://doi.org/10.1126/science.aad7154
- Physiological Differentiation within a Single-Species Biofilm Fueled by Serpentinization W. Brazelton et al. https://doi.org/10.1128/mBio.00127-11
- Quantitative analysis of anaerobic oxidation of methane (AOM) in marine sediments: A modeling perspective P. Regnier et al. https://doi.org/10.1016/j.earscirev.2011.01.002
- Methane oxidation by anaerobic archaea for conversion to liquid fuels T. Mueller et al. https://doi.org/10.1007/s10295-014-1548-7
- Microbial Ecology of the Dark Ocean above, at, and below the Seafloor B. Orcutt et al. https://doi.org/10.1128/MMBR.00039-10
- Microbial methane cycling in a terrestrial mud volcano in eastern Taiwan Y. Chang et al. https://doi.org/10.1111/j.1462-2920.2011.02658.x
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