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Diffusion of H2S from anaerobic thiolated ligand biodegradation rapidly generates bioavailable mercury
dc.contributor.authorStenzler, Benjamin R.
dc.contributor.authorZhang, Rui
dc.contributor.authorSemrau, Jeremy D.
dc.contributor.authorDiSpirito, Alan A.
dc.contributor.authorPoulain, Alexandre J.
dc.date.accessioned2022-08-02T18:57:20Z
dc.date.available2023-08-02 14:57:19en
dc.date.available2022-08-02T18:57:20Z
dc.date.issued2022-07
dc.identifier.citationStenzler, Benjamin R.; Zhang, Rui; Semrau, Jeremy D.; DiSpirito, Alan A.; Poulain, Alexandre J. (2022). "Diffusion of H2S from anaerobic thiolated ligand biodegradation rapidly generates bioavailable mercury." Environmental Microbiology 24(7): 3212-3228.
dc.identifier.issn1462-2912
dc.identifier.issn1462-2920
dc.identifier.urihttps://hdl.handle.net/2027.42/173106
dc.publisherJohn Wiley & Sons, Inc.
dc.titleDiffusion of H2S from anaerobic thiolated ligand biodegradation rapidly generates bioavailable mercury
dc.typeArticle
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelMicrobiology and Immunology
dc.subject.hlbtoplevelScience
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/173106/1/emi16078.pdf
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/173106/2/emi16078_am.pdf
dc.identifier.doi10.1111/1462-2920.16078
dc.identifier.sourceEnvironmental Microbiology
dc.identifier.citedreferenceSchuster, P.F., Schaefer, K.M., Aiken, G.R., Antweiler, R.C., Dewild, J.F., Gryziec, J.D., et al. ( 2018 ) Permafrost stores a globally significant amount of mercury. Geophys Res Lett 45: 1463 – 1471.
dc.identifier.citedreferenceSong, Y., Jiang, T., Liem-Nguyen, V., Sparrman, T., Björn, E., and Skyllberg, U. ( 2018 ) Thermodynamics of Hg(II) bonding to thiol groups in Suwannee River natural organic matter resolved by competitive ligand exchange, Hg LIII-edge EXAFS and 1H NMR spectroscopy. Environ Sci Technol 52: 8292 – 8301.
dc.identifier.citedreferenceStenzler, B. R., Gaudet, J., and Poulain, A. J. ( 2018 ). An Anaerobic Biosensor Assay for the Detection of Mercury and Cadmium. Journal of Visualized Experiments, 142. https://doi.org/10.3791/58324
dc.identifier.citedreferenceSunderland, E. M., Krabbenhoft, D. P., Moreau, J. W., Strode, S. A., and Landing, W. M. ( 2009 ). Mercury sources, distribution, and bioavailability in the North Pacific Ocean: Insights from data and models. Global Biogeochemical Cycles, 23 ( 2 ). https://doi.org/10.1029/2008gb003425
dc.identifier.citedreferenceSzczuka, A., Morel, F.M.M., and Schaefer, J.K. ( 2015 ) Effect of thiols, zinc, and redox conditions on Hg uptake in Shewanella oneidensis. Environ Sci Technol 49: 7432 – 7438.
dc.identifier.citedreferenceTang, Z., Fan, F., Deng, S., and Wang, D. ( 2020 ) Mercury in rice paddy fields and how does some agricultural activities affect the translocation and transformation of mercury – a critical review. Ecotoxicol Environ Saf 202: 110950.
dc.identifier.citedreferenceThe UniProt Consortium. ( 2021 ) UniProt: the universal protein knowledgebase in 2021. Nucleic Acids Res 49: D480 – D489.
dc.identifier.citedreferenceThomas, S.A., Catty, P., Hazemann, J.-L., Michaud-Soret, I., and Gaillard, J.-F. ( 2019 ) The role of cysteine and sulfide in the interplay between microbial Hg(II) uptake and sulfur metabolism†. Metallomics 11: 1219 – 1229.
dc.identifier.citedreferenceThomas, S.A., Mishra, B., and Myneni, S.C.B. ( 2020 ) Cellular mercury coordination environment, and not cell surface ligands, influence bacterial methylmercury production. Environ Sci Technol 54: 3960 – 3968.
dc.identifier.citedreferenceThomas, S.A., Rodby, K.E., Roth, E.W., Wu, J., and Gaillard, J.F. ( 2018 ) Spectroscopic and microscopic evidence of biomediated HgS species formation from Hg(II)-cysteine complexes: implications for Hg(II) bioavailability. Environ Sci Technol 52: 10030 – 10039.
dc.identifier.citedreferenceThomas, S.A., Tong, T., and Gaillard, J.-F. ( 2014 ) Hg(II) bacterial biouptake: the role of anthropogenic and biogenic ligands present in solution and spectroscopic evidence of ligand exchange reactions at the cell surface. Metallomics 6: 2213 – 2222.
dc.identifier.citedreferenceTian, L., Guan, W., Ji, Y., He, X., Chen, W., Alvarez, P.J.J., and Zhang, T. ( 2021 ) Microbial methylation potential of mercury sulfide particles dictated by surface structure. Nat Geosci 14: 409 – 416.
dc.identifier.citedreferenceVorobev, A., Jagadevan, S., Baral Bipin, S., DiSpirito Alan, A., Freemeier Brittani, C., Bergman Brandt, H., et al. ( 2013 ) Detoxification of mercury by Methanobactin from Methylosinus trichosporium OB3b. Appl Environ Microbiol 79: 5918 – 5926.
dc.identifier.citedreferenceYin, X., Wang, L., Zhang, L., Chen, H., Liang, X., Lu, X., et al. ( 2020 ) Synergistic effects of a chalkophore, methanobactin, on microbial methylation of mercury. Appl Environ Microbiol 86: e00122-00120.
dc.identifier.citedreferenceYu, Q., Szymanowski, J., Myneni, S.C.B., and Fein, J.B. ( 2014 ) Characterization of sulfhydryl sites within bacterial cell envelopes using selective site-blocking and potentiometric titrations. Chem Geol 373: 50 – 58.
dc.identifier.citedreferenceYu, R.-Q., Reinfelder, J.R., Hines, M.E., and Barkay, T. ( 2013 ) Mercury methylation by the methanogen Methanospirillum hungatei. Appl Environ Microbiol 79: 6325 – 6330.
dc.identifier.citedreferenceZhang, Z., Si, R., Lv, J., Ji, Y., Chen, W., Guan, W., et al. ( 2020 ) Effects of extracellular polymeric substances on the formation and methylation of mercury sulfide nanoparticles. Environ Sci Technol 54: 8061 – 8071.
dc.identifier.citedreferenceZhao, L., Chen, H., Lu, X., Lin, H., Christensen, G.A., and Pierce, E.M. ( 2017 ) Contrasting effects of dissolved organic matter on mercury methylation by Geobacter sulfurreducens PCA and Desulfovibrio desulfuricans ND132. Environ Sci Technol 51: 10468 – 10475.
dc.identifier.citedreferenceZhou, J., Smith, M.D., Cooper, S.J., Cheng, X., Smith, J.C., and Parks, J.M. ( 2017 ) Modeling of the passive permeation of mercury and methylmercury complexes through a bacterial cytoplasmic membrane. Environ Sci Technol 51: 10595 – 10604.
dc.identifier.citedreferenceAdediran, G.A., Liem-Nguyen, V., Song, Y., Schaefer, J.K., Skyllberg, U., and Björn, E. ( 2019 ) Microbial biosynthesis of thiol compounds: implications for speciation, cellular uptake, and methylation of Hg(II). Environ Sci Technol 53: 8187 – 8196.
dc.identifier.citedreferenceAn, J., Zhang, L., Lu, X., Pelletier, D.A., Pierce, E.M., Johs, A., et al. ( 2019 ) Mercury uptake by Desulfovibrio desulfuricans ND132: passive or active? Environ Sci Technol 53: 6264 – 6272.
dc.identifier.citedreferenceBalls, P.W., and Liss, P.S. ( 1983 ) Exchange of H 2 S between water and air. Atmos Environ 1967: 735 – 742.
dc.identifier.citedreferenceBandow, N.L., Gallagher, W.H., Behling, L., Choi, D.W., Semrau, J.D., Hartsel, S.C., et al. ( 2011 ) Isolation of methanobactin from the spent media of methane-oxidizing bacteria. Methods Enzymol 495: 259 – 269.
dc.identifier.citedreferenceBaral, B.S., Bandow, N.L., Vorobev, A., Freemeier, B.C., Bergman, B.H., Herdendorf, T.J., et al. ( 2014 ) Mercury binding by methanobactin from Methylocystis strain SB2. J Inorg Biochem 141: 161 – 169.
dc.identifier.citedreferenceBeulig, F., Røy, H., McGlynn, S.E., and Jørgensen, B.B. ( 2019 ) Cryptic CH 4 cycling in the sulfate–methane transition of marine sediments apparently mediated by ANME-1 archaea. ISME J 13: 250 – 262.
dc.identifier.citedreferenceBjørklund, G., Crisponi, G., Nurchi, V.M., Cappai, R., Buha Djordjevic, A., and Aaseth, J. ( 2019 ) A review on coordination properties of thiol-containing chelating agents towards mercury, cadmium, and lead. Molecules 24: 3247.
dc.identifier.citedreferenceBranfireun, B.A., Cosio, C., Poulain, A.J., Riise, G., and Bravo, A.G. ( 2020 ) Mercury cycling in freshwater systems – an updated conceptual model. Sci Total Environ 745: 140906.
dc.identifier.citedreferenceBravo, A.G., Cosio, C., Amouroux, D., Zopfi, J., Chevalley, P.-A., Spangenberg, J.E., et al. ( 2014 ) Extremely elevated methyl mercury levels in water, sediment and organisms in a Romanian reservoir affected by release of mercury from a chlor-alkali plant. Water Res 49: 391 – 405.
dc.identifier.citedreferenceCarrasco-Gil, S., Alvarez-Fernández, A., Sobrino-Plata, J., Millán, R., Carpena-Ruiz, R.O., Leduc, D.L., et al. ( 2011 ) Complexation of Hg with phytochelatins is important for plant Hg tolerance. Plant Cell Environ 34: 778 – 791.
dc.identifier.citedreferenceChiasson-Gould, S.A., Blais, J.M., and Poulain, A.J. ( 2014 ) Dissolved organic matter kinetically controls mercury bioavailability to bacteria. Environ Sci Technol 48: 3153 – 3161.
dc.identifier.citedreferenceChoi, U., and Lee, C.-R. ( 2019 ) Distinct roles of outer membrane porins in antibiotic resistance and membrane integrity in Escherichia coli. Front Microbiol 10: 953.
dc.identifier.citedreferenceColombo, M.J., Ha, J., Reinfelder, J.R., Barkay, T., and Yee, N. ( 2013 ) Anaerobic oxidation of Hg(0) and methylmercury formation by Desulfovibrio desulfuricans ND132. Geochim Cosmochim Acta 112: 166 – 177.
dc.identifier.citedreferenceDeonarine, A., and Hsu-Kim, H. ( 2009 ) Precipitation of mercuric sulfide nanoparticles in NOM-containing water: implications for the natural environment. Environ Sci Technol 43: 2368 – 2373.
dc.identifier.citedreferenceDiaz, R.J., and Rosenberg, R. ( 2008 ) Spreading dead zones and consequences for marine ecosystems. Science 321: 926 – 929.
dc.identifier.citedreferenceDranguet, P., Slaveykova, V.I., and Le Faucheur, S. ( 2018 ) Kinetics of mercury accumulation by freshwater biofilms. Environ Chem 14: 458 – 467.
dc.identifier.citedreferenceDriscoll, C.T., Mason, R.P., Chan, H.M., Jacob, D.J., and Pirrone, N. ( 2013 ) Mercury as a global pollutant: sources, pathways, and effects. Environ Sci Technol 47: 4967 – 4983.
dc.identifier.citedreferenceDrott, A., Bjorn, E., Bouchet, S., and Skyllberg, U. ( 2013 ) Refining thermodynamic constants for mercury (II)-sulfides in equilibrium with metacinnabar at sub-micromolar aqueous sulfide concentrations. Environ Sci Technol 47: 4197 – 4203.
dc.identifier.citedreferenceDunham-Cheatham, S., Mishra, B., Myneni, S., and Fein, J.B. ( 2015 ) The effect of natural organic matter on the adsorption of mercury to bacterial cells. Geochim Cosmochim Acta 150: 1 – 10.
dc.identifier.citedreferenceEnescu, M., Nagy, K.L., and Manceau, A. ( 2016 ) Nucleation of mercury sulfide by dealkylation. Sci Rep 6: 39359.
dc.identifier.citedreferenceFein, J.B., Yu, Q., Nam, J., and Yee, N. ( 2019 ) Bacterial cell envelope and extracellular sulfhydryl binding sites: their roles in metal binding and bioavailability. Chem Geol 521: 28 – 38.
dc.identifier.citedreferenceGlazyrina, J., Materne, E.M., Dreher, T., Storm, D., Junne, S., Adams, T., et al. ( 2010 ) High cell density cultivation and recombinant protein production with Escherichia coli in a rocking-motion-type bioreactor. Microb Cell Factories 9: 42.
dc.identifier.citedreferenceGraham, A.M., Aiken, G.R., and Gilmour, C.C. ( 2012 ) Dissolved organic matter enhances microbial mercury methylation under sulfidic conditions. Environ Sci Technol 46: 2715 – 2723.
dc.identifier.citedreferenceGraham, A.M., Aiken, G.R., and Gilmour, C.C. ( 2013 ) Effect of dissolved organic matter source and character on microbial Hg methylation in Hg–S–DOM solutions. Environ Sci Technol 47: 5746 – 5754.
dc.identifier.citedreferenceGrégoire, D.S., Lavoie, N.C., and Poulain, A.J. ( 2018 ) Heliobacteria reveal fermentation as a key pathway for mercury reduction in anoxic environments. Environ Sci Technol 52: 4145 – 4153.
dc.identifier.citedreferenceGrégoire, D.S., and Poulain, A.J. ( 2018 ) Shining light on recent advances in microbial mercury cycling. FACETS 3: 858 – 879.
dc.identifier.citedreferenceHinckley, E.-L.S., Crawford, J.T., Fakhraei, H., and Driscoll, C.T. ( 2020 ) A shift in sulfur-cycle manipulation from atmospheric emissions to agricultural additions. Nat Geosci 13: 597 – 604.
dc.identifier.citedreferenceHinz, A.J., Stenzler, B., Poulain, A.J., and Bose, A. ( 2022 ) Golden gate assembly of aerobic and anaerobic microbial bioreporters. Appl Environ Microbiol 88: e01485-01421.
dc.identifier.citedreferenceHsu-Kim, H., Kucharzyk, K.H., Zhang, T., and Deshusses, M.A. ( 2013 ) Mechanisms regulating mercury bioavailability for methylating microorganisms in the aquatic environment: a critical review. Environ Sci Technol 47: 2441 – 2456.
dc.identifier.citedreferenceHu, H., Lin, H., Zheng, W., Rao, B., Feng, X., Liang, L., et al. ( 2013a ) Mercury reduction and cell-surface adsorption by geobacter sulfurreducens PCA. Environ Sci Technol 47: 10922 – 10930.
dc.identifier.citedreferenceHu, H., Lin, H., Zheng, W., Tomanicek, S.J., Johs, A., Feng, X., et al. ( 2013b ) Oxidation and methylation of dissolved elemental mercury by anaerobic bacteria. Nat Geosci 6: 751 – 754.
dc.identifier.citedreferenceHuynh, K., Liem-Nguyen, V., Feng, C., Lindberg, R., and Björn, E. ( 2020 ) Quantification of total concentration of thiol functional groups in environmental samples by titration with monobromo(trimethylammonio)bimane and determination with tandem mass spectrometry. Talanta 218: 121109.
dc.identifier.citedreferenceJørgensen, B.B., Findlay, A.J., and Pellerin, A. ( 2019 ) The biogeochemical sulfur cycle of marine sediments. Front Microbiol 10: 849.
dc.identifier.citedreferenceKalidass, B., Ul-Haque, M.F., Baral, B.S., DiSpirito, A.A., and Semrau, J.D. ( 2015 ) Competition between metals for binding to methanobactin enables expression of soluble methane monooxygenase in the presence of copper. Appl Environ Microbiol 81: 1024 – 1031.
dc.identifier.citedreferenceKawakami, S.K., Gledhill, M., and Achterberg, E.P. ( 2006 ) Production of phytochelatins and glutathione by marine phytoplankton in response to metal stress 1. J Phycol 42: 975 – 989.
dc.identifier.citedreferenceLabrenz, M., Druschel, G.K., Thomsen-Ebert, T., Gilbert, B., Welch, S.A., Kemner, K.M., et al. ( 2000 ) Formation of Sphalerite (ZnS) deposits in natural biofilms of sulfate-reducing bacteria. Science 290: 1744 – 1747.
dc.identifier.citedreferenceLeclerc, M., Planas, D., and Amyot, M. ( 2015 ) Relationship between extracellular low-molecular-weight thiols and mercury species in natural Lake Periphytic biofilms. Environ Sci Technol 49: 7709 – 7716.
dc.identifier.citedreferenceLehnherr, I., St, V.L., Louis, H.H., and Kirk, J.L. ( 2011 ) Methylation of inorganic mercury in polar marine waters. Nat Geosci 4: 298 – 302.
dc.identifier.citedreferenceLiem-Nguyen, V., Skyllberg, U., and Björn, E. ( 2017a ) Thermodynamic modeling of the solubility and chemical speciation of mercury and methylmercury driven by organic thiols and micromolar sulfide concentrations in boreal wetland soils. Environ Sci Technol 51: 3678 – 3686.
dc.identifier.citedreferenceLiem-Nguyen, V., Skyllberg, U., Nam, K., and Björn, E. ( 2017b ) Thermodynamic stability of mercury(II) complexes formed with environmentally relevant low-molecular-mass thiols studied by competing ligand exchange and density functional theory. Environ Chem 14: 243 – 253.
dc.identifier.citedreferenceLin, H., Lu, X., Liang, L., and Gu, B. ( 2015 ) Cysteine inhibits mercury methylation by Geobacter sulfurreducens PCA mutant ΔomcBESTZ. Environ Sci Technol Lett 2: 144 – 148.
dc.identifier.citedreferenceLiu, Y.-R., Lu, X., Zhao, L., An, J., He, J.-Z., Pierce, E.M., et al. ( 2016 ) Effects of cellular sorption on mercury bioavailability and methylmercury production by Desulfovibrio desulfuricans ND132. Environ Sci Technol 50: 13335 – 13341.
dc.identifier.citedreferenceManceau, A., Lemouchi, C., Enescu, M., Gaillot, A.-C., Lanson, M., Magnin, V., et al. ( 2015 ) Formation of mercury sulfide from Hg(II)–thiolate complexes in natural organic matter. Environ Sci Technol 49: 9787 – 9796.
dc.identifier.citedreferenceMangal, V., Stock, N.L., and Guéguen, C. ( 2016 ) Molecular characterization of phytoplankton dissolved organic matter (DOM) and sulfur components using high resolution Orbitrap mass spectrometry. Anal Bioanal Chem 408: 1891 – 1900.
dc.identifier.citedreferenceMazrui, N.M., Seelen, E., King’ondu, C.K., Thota, S., Awino, J., Rouge, J., et al. ( 2018 ) The precipitation, growth and stability of mercury sulfide nanoparticles formed in the presence of marine dissolved organic matter. Environ Sci Process Impacts 20: 642 – 656.
dc.identifier.citedreferenceMills, J.V., Antler, G., and Turchyn, A.V. ( 2016 ) Geochemical evidence for cryptic sulfur cycling in salt marsh sediments. Earth Planet Sci Lett 453: 23 – 32.
dc.identifier.citedreferenceMishra, B., Shoenfelt, E., Yu, Q., Yee, N., Fein, J.B., and Myneni, S.C.B. ( 2017 ) Stoichiometry of mercury-thiol complexes on bacterial cell envelopes. Chem Geol 464: 137 – 146.
dc.identifier.citedreferenceNdu, U., Barkay, T., Mason, R.P., Schartup, A.T., Al-Farawati, R., Liu, J., and Reinfelder, J.R. ( 2015 ) The use of a mercury biosensor to evaluate the bioavailability of mercury-thiol complexes and mechanisms of mercury uptake in bacteria. PLoS One 10: e0138333.
dc.identifier.citedreferenceNdu, U., Mason, R.P., Zhang, H., Lin, S., and Visscher, P.T. ( 2012 ) Effect of inorganic and organic ligands on the bioavailability of methylmercury as determined by using a mer-lux bioreporter. Appl Environ Microbiol 78: 7276 – 7282.
dc.identifier.citedreferenceObrist, D., Kirk, J.L., Zhang, L., Sunderland, E.M., Jiskra, M., and Selin, N.E. ( 2018 ) A review of global environmental mercury processes in response to human and natural perturbations: changes of emissions, climate, and land use. Ambio 47: 116 – 140.
dc.identifier.citedreferenceOlsen, T.A., Brandt, C.C., and Brooks, S.C. ( 2016 ) Periphyton biofilms influence net methylmercury production in an industrially contaminated system. Environ Sci Technol 50: 10843 – 10850.
dc.identifier.citedreferenceOrtiz, V.L., Mason, R.P., and Ward, J.E. ( 2015 ) An examination of the factors influencing mercury and methylmercury particulate distributions, methylation and demethylation rates in laboratory-generated marine snow. Mar Chem 177: 753 – 762.
dc.identifier.citedreferenceParkhurst, D.L.A. ( 2013 ) Description of Input and Examples for PHREEQC Version 3 – A Computer Program for Speciation, Batch-Reaction, One-Dimensional Transport, and Inverse Geochemical Calculations. Reston, Virginia: U.S. Department of the Interior, U.S. Geological Survey, p. 497.
dc.identifier.citedreferencePester, M., Knorr, K.-H., Friedrich, M., Wagner, M., and Loy, A. ( 2012 ) Sulfate-reducing microorganisms in wetlands – fameless actors in carbon cycling and climate change. Front Microbiol 3: 72.
dc.identifier.citedreferencePham, A.L.-T., Morris, A., Zhang, T., Ticknor, J., Levard, C., and Hsu-Kim, H. ( 2014 ) Precipitation of nanoscale mercuric sulfides in the presence of natural organic matter: structural properties, aggregation, and biotransformation. Geochim Cosmochim Acta 133: 204 – 215.
dc.identifier.citedreferencePodar, M., Gilmour, C.C., Brandt, C.C., Soren, A., Brown, S.D., Crable, B.R., et al. ( 2015 ) Global prevalence and distribution of genes and microorganisms involved in mercury methylation. Sci Adv 1: e1500675.
dc.identifier.citedreferencePoulin, B.A., Gerbig, C.A., Kim, C.S., Stegemeier, J.P., Ryan, J.N., and Aiken, G.R. ( 2017 ) Effects of sulfide concentration and dissolved organic matter characteristics on the structure of nanocolloidal metacinnabar. Environ Sci Technol 51: 13133 – 13142.
dc.identifier.citedreferenceRaven, M.R., Keil, R.G., and Webb, S.M. ( 2021 ) Microbial sulfate reduction and organic sulfur formation in sinking marine particles. Science 371: 178 – 181.
dc.identifier.citedreferenceRegnell, O., and Watras, C.J. ( 2019 ) Microbial mercury methylation in aquatic environments: a critical review of published field and laboratory studies. Environ Sci Technol 53: 4 – 19.
dc.identifier.citedreferenceSchaefer, J.K., and Morel, F.M.M. ( 2009 ) High methylation rates of mercury bound to cysteine by Geobacter sulfurreducens. Nat Geosci 2: 123 – 126.
dc.identifier.citedreferenceSchaefer, J.K., Rocks, S.S., Zheng, W., Liang, L., Gu, B., and Morel, F.M.M. ( 2011 ) Active transport, substrate specificity, and methylation of Hg(II) in anaerobic bacteria. Proc Natl Acad Sci U S A 108: 8714 – 8719.
dc.identifier.citedreferenceSchaefer, J.K., Szczuka, A., and Morel, F.M.M. ( 2014 ) Effect of divalent metals on Hg(II) uptake and methylation by bacteria. Environ Sci Technol 48: 3007 – 3013.
dc.identifier.citedreferenceSchwarzenbach, R.P., Gschwend, P.M., and Imboden, D.M. ( 2002 ) Air–water exchange. In Environmental Organic Chemistry, Schwarzenbach, R.P., Gschwend, P.M., and Imboden, D.M. (eds). Hoboken, NJ: John Wiley & Sons, Inc. https://doi.org/10.1002/0471649643.ch20.
dc.identifier.citedreferenceSemrau, J., and Gu, B. ( 2020 ). Methanotrophic-Mediated Methylmercury Transformation: Characterization of Products, Mechanism, and Environmental Significance (Final Technical Report). https://doi.org/10.2172/1692379
dc.identifier.citedreferenceShakeri Yekta, S., Svensson, B.H., Björn, A., and Skyllberg, U. ( 2014 ) Thermodynamic modeling of iron and trace metal solubility and speciation under sulfidic and ferruginous conditions in full scale continuous stirred tank biogas reactors. Appl Geochem 47: 61 – 73.
dc.identifier.citedreferenceSi, Y., Zou, Y., Liu, X., Si, X., and Mao, J. ( 2015 ) Mercury methylation coupled to iron reduction by dissimilatory iron-reducing bacteria. Chemosphere 122: 206 – 212.
dc.identifier.citedreferenceSong, Y., Adediran, G.A., Jiang, T., Hayama, S., Björn, E., and Skyllberg, U. ( 2020 ) Toward an internally consistent model for Hg(II) chemical speciation calculations in bacterium–natural organic matter–low molecular mass thiol systems. Environ Sci Technol 54: 8094 – 8103.
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