The interplay of microbially mediated and abiotic reactions in the biogeochemical Fe cycle

Extracellular electron transfer via microbial nanowires

Reguera, G., McCarthy, K. D., Mehta, T., Nicoll, J. S., Tuominen, M. T., & Lovley, D. R. (2005) · Nature · doi:10.1038/nature03661 · Cited by 2,590 · see citing works

The catalytic decomposition of hydrogen peroxide by iron salts

Haber, F., & Weiss, J. (1934) · Proceedings of the Royal Society of London. Series A - Mathematical and Physical Sciences · doi:10.1098/rspa.1934.0221 · Cited by 2,571 · see citing works

Novel Mode of Microbial Energy Metabolism: Organic Carbon Oxidation Coupled to Dissimilatory Reduction of Iron or Manganese

Lovley, D. R., & Phillips, E. J. P. (1988) · Applied and Environmental Microbiology · doi:10.1128/aem.54.6.1472-1480.1988 · Cited by 2,395 · see citing works

How antibiotics kill bacteria: from targets to networks

Kohanski, M. A., Dwyer, D. J., & Collins, J. J. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2333 · Cited by 2,266 · see citing works

Natural Antibiotic Resistance and Contamination by Antibiotic Resistance Determinants: The Two Ages in the Evolution of Resistance to Antimicrobials

Martínez, J. L. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00001 · Cited by 2,101 · see citing works

Shewanella secretes flavins that mediate extracellular electron transfer

Marsili, E., Baron, D. B., Shikhare, I. D., Coursolle, D., Gralnick, J. A., & Bond, D. R. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0710525105 · Cited by 1,999 · see citing works

Humic substances as electron acceptors for microbial respiration

Lovley, D. R., Coates, J. D., Blunt-Harris, E. L., Phillips, E. J. P., & Woodward, J. C. (1996) · Nature · doi:10.1038/382445a0 · Cited by 1,834 · see citing works

Electrically conductive bacterial nanowires produced by <i>Shewanella oneidensis</i> strain MR-1 and other microorganisms

Gorby, Y. A., Yanina, S., McLean, J. S., Rosso, K. M., Moyles, D., Dohnalkova, A., Beveridge, T. J., Chang, I. S., Kim, B. H., Kim, K. S., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604517103 · Cited by 1,749 · see citing works

Preservation of organic matter in sediments promoted by iron

Lalonde, K., Mucci, A. O., Ouellet, A., & Gélinas, Y. (2012) · Nature · doi:10.1038/nature10855 · Cited by 1,524 · see citing works

Biogeochemical Redox Processes and their Impact on Contaminant Dynamics

Borch, T., Kretzschmar, R., Kappler, A., Cappellen, P. V., Ginder-Vogel, M., Voegelin, A., & Campbell, K. (2010) · Environmental Science &amp; Technology · doi:10.1021/es9026248 · Cited by 1,456 · see citing works

Nucleic acid-based approaches to investigate microbial-related cheese quality defects

O'Sullivan, D. J., Giblin, L. M., McSweeney, P. L. H., Sheehan, J. J., & Cotter, P. D. (2013) · Frontiers in Microbiology · doi:10.3389/fmicb.2013.00001 · Cited by 1,423 · see citing works

Reactive iron in marine sediments

Canfield, D. E. (1989) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(89)90005-7 · Cited by 1,081 · see citing works

Anaerobic production of magnetite by a dissimilatory iron-reducing microorganism

Lovley, D. R., Stolz, J. F., Nord, G. L., & Phillips, E. J. P. (1987) · Nature · doi:10.1038/330252a0 · Cited by 989 · see citing works

Anaerobic, nitrate-dependent microbial oxidation of ferrous iron

Straub, K. L., Benz, M., Schink, B., & Widdel, F. (1996) · Applied and Environmental Microbiology · doi:10.1128/aem.62.4.1458-1460.1996 · Cited by 927 · see citing works

Tunable metallic-like conductivity in microbial nanowire networks

Malvankar, N. S., Vargas, M., Nevin, K. P., Franks, A. E., Leang, C., Kim, B., Inoue, K., Mester, T., Covalla, S. F., Johnson, J. P., et al. (2011) · Nature Nanotechnology · doi:10.1038/nnano.2011.119 · Cited by 915 · see citing works

Secretion of Flavins by Shewanella Species and Their Role in Extracellular Electron Transfer

von Canstein, H., Ogawa, J., Shimizu, S., & Lloyd, J. R. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.01387-07 · Cited by 892 · see citing works

Genome sequence of the dissimilatory metal ion–reducing bacterium Shewanella oneidensis

Heidelberg, J. F., Paulsen, I. T., Nelson, K. E., Gaidos, E. J., Nelson, W. C., Read, T. D., Eisen, J. A., Seshadri, R., Ward, N. L., Methé, B. A., et al. (2002) · Nature Biotechnology · doi:10.1038/nbt749 · Cited by 862 · see citing works

Extending the Upper Temperature Limit for Life

Kashefi, K., & Lovley, D. R. (2003) · Science · doi:10.1126/science.1086823 · Cited by 770 · see citing works

Ferrous iron oxidation by anoxygenic phototrophic bacteria

Widdel, F., Schnell, S., Heising, S., Ehrenreich, A., Assmus, B., & Schink, B. (1993) · Nature · doi:10.1038/362834a0 · Cited by 735 · see citing works

Genome of Geobacter sulfurreducens: Metal Reduction in Subsurface Environments

Methé, B. A., Nelson, W. C., Eisen, J. A., Paulsen, I. T., Nelson, W. C., Heidelberg, J. F., Wu, D., Wu, M., Ward, N. L., Beanan, M. J., et al. (2003) · Science · doi:10.1126/science.1088727 · Cited by 710 · see citing works

Geobacter

Lovley, D. R., Ueki, T., Zhang, T., Malvankar, N. S., Shrestha, P. M., Flanagan, K. A., Aklujkar, M., Butler, J. E., Giloteaux, L., Rotaru, A., et al. (2011) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/b978-0-12-387661-4.00004-5 · Cited by 700 · see citing works

Manganese, iron and sulfur cycling in a coastal marine sediment, Aarhus bay, Denmark

Thamdrup, B., Fossing, H., & Jørgensen, B. B. (1994) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(94)90298-4 · Cited by 693 · see citing works

Respiration of metal (hydr)oxides by Shewanella and Geobacter: a key role for multihaem c‐type cytochromes

Shi, L., Squier, T. C., Zachara, J. M., & Fredrickson, J. K. (2007) · Molecular Microbiology · doi:10.1111/j.1365-2958.2007.05783.x · Cited by 664 · see citing works

Bacterial Manganese and Iron Reduction in Aquatic Sediments

Thamdrup, B. (2000) · Advances in Microbial Ecology · doi:10.1007/978-1-4615-4187-5_2 · Cited by 659 · see citing works

Microbial interspecies electron transfer via electric currents through conductive minerals

Kato, S., Hashimoto, K., & Watanabe, K. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1117592109 · Cited by 647 · see citing works

Isolation and characterization of novel iron-oxidizing bacteria that grow at circumneutral pH

Emerson, D., & Moyer, C. (1997) · Applied and Environmental Microbiology · doi:10.1128/aem.63.12.4784-4792.1997 · Cited by 579 · see citing works

Extracellular electron transfer

Hernandez, M. E., & Newman, D. K. (2001) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000796 · Cited by 579 · see citing works

Electric currents couple spatially separated biogeochemical processes in marine sediment

Nielsen, L. P., Risgaard‐Petersen, N., Fossing, H., Christensen, P. B., & Sayama, M. (2010) · Nature · doi:10.1038/nature08790 · Cited by 565 · see citing works

Extracellular electron transfer through microbial reduction of solid-phase humic substances

Roden, E., Kappler, A. A., Bauer, I., Jian, J., Paul, A., STOESSER, R., Konishi, H., & Xu, H. (2010) · Nature Geoscience · doi:10.1038/ngeo870 · Cited by 511 · see citing works

Deposition of banded iron formations by anoxygenic phototrophic Fe(II)-oxidizing bacteria

Kappler, A., Pasquero, C., Konhauser, K. O., & Newman, D. K. (2005) · Geology · doi:10.1130/g21658.1 · Cited by 501 · see citing works

Photochemical cycling of iron in the surface ocean mediated by microbial iron(iii)-binding ligands

Barbeau, K. A., Rue, E. L., Bruland, K. W., & Butler, A. (2001) · Nature · doi:10.1038/35096545 · Cited by 498 · see citing works

Anaerobic oxidation of ferrous iron by purple bacteria, a new type of phototrophic metabolism

Ehrenreich, A., & Widdel, F. (1994) · Applied and Environmental Microbiology · doi:10.1128/aem.60.12.4517-4526.1994 · Cited by 495 · see citing works

Characterization of an electron conduit between bacteria and the extracellular environment

Hartshorne, R. S., Reardon, C. L., Ross, D. E., Nuester, J., Clarke, T. A., Gates, A. J., Mills, P. C., Fredrickson, J. K., Zachara, J. M., Shi, L., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900086106 · Cited by 491 · see citing works

Nitrogen loss from soil through anaerobic ammonium oxidation coupled to iron reduction

Yang, W. H., Weber, K. A., & Silver, W. L. (2012) · Nature Geoscience · doi:10.1038/ngeo1530 · Cited by 461 · see citing works

Geobacter metallireducens accesses insoluble Fe(iii) oxide by chemotaxis

Childers, S. E., Ciufo, S., & Lovley, D. R. (2002) · Nature · doi:10.1038/416767a · Cited by 453 · see citing works

Short-term compassion training increases prosocial behavior in a newly developed prosocial game

Leiberg, S., Klimecki, O., & Singer, T. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017798 · Cited by 442 · see citing works

Microbial Polysaccharides Template Assembly of Nanocrystal Fibers

Chan, C. S., De Stasio, G., Welch, S. A., Girasole, M., Frazer, B. H., Nesterova, M. V., Fakra, S., & Banfield, J. F. (2004) · Science · doi:10.1126/science.1092098 · Cited by 423 · see citing works

Bioenergetic challenges of microbial iron metabolisms

Bird, L. J., Bonnefoy, V., & Newman, D. K. (2011) · Trends in Microbiology · doi:10.1016/j.tim.2011.05.001 · Cited by 420 · see citing works

Sulfide oxidation under chemolithoautotrophic denitrifying conditions

Beristain-Cardoso, R., Sierra‐Álvarez, R., Rowlette, P. C., et al. (2006) · Biotechnology and Bioengineering · doi:10.1002/bit.21084 · Cited by 386 · see citing works

Geothrix fermentans gen. nov., sp. nov., a novel Fe(III)-reducing bacterium from a hydrocarbon-contaminated aquifer

Coates, J. D., Ellis, D. J., Gaw, C. V., & Lovley, D. R. (1999) · International Journal of Systematic and Evolutionary Microbiology · doi:10.1099/00207713-49-4-1615 · Cited by 382 · see citing works

Lithotrophic iron-oxidizing bacteria produce organic stalks to control mineral growth: implications for biosignature formation.

Chan, C. S., Fakra, S. C., Emerson, D., Fleming, E. J., & Edwards, K. J. (2011) · The ISME Journal · doi:10.1038/ismej.2010.173 · Cited by 377 · see citing works

Widespread Production of Extracellular Superoxide by Heterotrophic Bacteria

Diaz, J. M., Hansel, C. M., Voelker, B. M., Mendes, C. M., Andeer, P. F., & Zhang, T. (2013) · Science · doi:10.1126/science.1237331 · Cited by 365 · see citing works

Effects of Fulvic Acid on Fe(II) Oxidation by Hydrogen Peroxide

Voelker, B. M., & Sulzberger, B. (1996) · Environmental Science & Technology · doi:10.1021/es9502132 · Cited by 363 · see citing works

Iron isotope fractionation by Fe(II)-oxidizing photoautotrophic bacteria 1 1Associate editor: D. E. Canfield

Croal, L. R., Johnson, C. M., Beard, B. L., & Newman, D. K. (2004) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2003.09.011 · Cited by 355 · see citing works

Isolation and Characterization of Novel Psychrophilic, Neutrophilic, Fe-Oxidizing, Chemolithoautotrophic α- and γ- Proteobacteria from the Deep Sea

Edwards, K. J., Rogers, D. R., Wirsen, C. O., & McCollom, T. M. (2003) · Applied and Environmental Microbiology · doi:10.1128/aem.69.5.2906-2913.2003 · Cited by 355 · see citing works

The roles of outer membrane cytochromes of Shewanella and Geobacter in extracellular electron transfer

Shi, L., Richardson, D. J., Wang, Z.-M., Kerisit, S., Rosso, K. M., Zachara, J. M., & Fredrickson, J. K. (2009) · Environmental Microbiology Reports · doi:10.1111/j.1758-2229.2009.00035.x · Cited by 354 · see citing works

Rates and Mechanism of Fe(II) Oxidation at Nanomolar Total Iron Concentrations

King, D. W., Lounsbury, H. A., & Millero, F. J. (1995) · Environmental Science & Technology · doi:10.1021/es00003a033 · Cited by 351 · see citing works

Alignment of the <i>c</i> -Type Cytochrome OmcS along Pili of <i>Geobacter sulfurreducens</i>

Leang, C., Qian, X., Mester, T., & Lovley, D. R. (2010) · Applied and Environmental Microbiology · doi:10.1128/aem.00023-10 · Cited by 342 · see citing works

Pulse radiolytic studies of the reaction of perhydroxyl/superoxide O2- with iron(II)/iron(III) ions. The reactivity of HO2/O2- with ferric ions and its implication on the occurrence of the Haber-Weiss reaction

Rush, J. D., & Bielski, B. H. J. (1985) · The Journal of Physical Chemistry · doi:10.1021/j100269a035 · Cited by 339 · see citing works

Shewanella oneidensis MR-1 Uses Overlapping Pathways for Iron Reduction at a Distance and by Direct Contact under Conditions Relevant for Biofilms

Lies, D. P., Hernandez, M. E., Kappler, A. A., Mielke, R. E., Gralnick, J. A., & Newman, D. K. (2005) · Applied and Environmental Microbiology · doi:10.1128/aem.71.8.4414-4426.2005 · Cited by 335 · see citing works

Formation of Fe(III)-minerals by Fe(II)-oxidizing photoautotrophic bacteria 1 1Associate editor: L. G. Benning

Kappler, A. A., & Newman, D. K. (2004) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2003.09.006 · Cited by 334 · see citing works

Biogeochemistry of pyrite and iron sulfide oxidation in marine sediments

Schippers, A., & Jørgensen, B. B. (2002) · Geochimica et Cosmochimica Acta · doi:10.1016/s0016-7037(01)00745-1 · Cited by 333 · see citing works

Mechanisms for Fe(III) Oxide Reduction in Sedimentary Environments

Nevin, K. P., & Lovley, D. R. (2002) · Geomicrobiology Journal · doi:10.1080/01490450252864253 · Cited by 330 · see citing works

Anaerobic redox cycling of iron by freshwater sediment microorganisms.

Weber, K., Urrutia, M., Churchill, P., Kukkadapu, R., & Roden, E. (2006) · Environmental Microbiology · doi:10.1111/j.1462-2920.2005.00873.x · Cited by 329 · see citing works

Ammonium oxidation coupled to dissimilatory reduction of iron under anaerobic conditions in wetland soils

Clement, J., Shrestha, J., Ehrenfeld, J., & Jaffé, P. (2005) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2005.03.027 · Cited by 326 · see citing works

Kinetics of Microbial and Chemical Reduction of Humic Substances: Implications for Electron Shuttling

Jian, J., & Kappler, A. A. (2008) · Environmental Science & Technology · doi:10.1021/es7023803 · Cited by 325 · see citing works

The kinetics of the oxidation of ferrous iron in synthetic and natural waters

Davison, W., & Seed, G. (1983) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(83)90091-1 · Cited by 320 · see citing works

Abundant Porewater Mn(III) Is a Major Component of the Sedimentary Redox System

Madison, A. S., Tebo, B. M., Mucci, A. O., Sundby, B., & Luther, G. W. (2013) · Science · doi:10.1126/science.1241396 · Cited by 307 · see citing works

Nitrite in soils: accumulation and role in the formation of gaseous N compounds

Cleemput, O. V., & Samater, A. H. (1995) · Nutrient Cycling in Agroecosystems · doi:10.1007/bf00749884 · Cited by 296 · see citing works

Oxidation of hydrogen sulfide by hydrous Fe(III) oxides in seawater

Yao, W., & Millero, F. J. (1996) · Marine Chemistry · doi:10.1016/0304-4203(95)00072-0 · Cited by 296 · see citing works

Microbial reduction of manganese oxides: Interactions with iron and sulfur

Myers, C. R., & Nealson, K. H. (1988) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(88)90041-5 · Cited by 294 · see citing works

Respiration-linked proton translocation coupled to anaerobic reduction of manganese(IV) and iron(III) in Shewanella putrefaciens MR-1

Myers, C. R., & Nealson, K. H. (1990) · Journal of Bacteriology · doi:10.1128/jb.172.11.6232-6238.1990 · Cited by 289 · see citing works

Recovery of Humic-Reducing Bacteria from a Diversity of Environments

Coates, J. D., Ellis, D. J., Blunt‐Harris, E. L., VanPraagh, C. G., Roden, E., & Lovley, D. R. (1998) · Applied and Environmental Microbiology · doi:10.1128/aem.64.4.1504-1509.1998 · Cited by 289 · see citing works

Long-range electron transport in Geobacter sulfurreducens biofilms is redox gradient-driven

Snider, R. M., Glaven, S. M., Tsoi, S. D., Erickson, J. S., & Tender, L. M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1209829109 · Cited by 274 · see citing works

Photoferrotrophs thrive in an Archean Ocean analogue

Crowe, S. A., Jones, C., Katsev, S., Magen, C., O'Neill, A. H., Sturm, A., Canfield, D. E., Haffner, G. D., Mucci, A., Sundby, B., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0805313105 · Cited by 264 · see citing works

Microbial Oxidation of Pyrite Coupled to Nitrate Reduction in Anoxic Groundwater Sediment

Jørgensen, C. J., Jacobsen, O. S., Elberling, B., et al. (2009) · Environmental Science & Technology · doi:10.1021/es803417s · Cited by 263 · see citing works

Abiotic oxidation of Fe( II ) by reactive nitrogen species in cultures of the nitrate‐reducing Fe( II ) oxidizer A cidovorax sp. BoFeN1 – questioning the existence of enzymatic Fe( II ) oxidation

Klueglein, N., & Kappler, A. A. (2012) · Geobiology · doi:10.1111/gbi.12019 · Cited by 262 · see citing works

Mn(II) oxidation by an ascomycete fungus is linked to superoxide production during asexual reproduction

Hansel, C. M., Zeiner, C. A., Santelli, C. M., & Webb, S. M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1203885109 · Cited by 259 · see citing works

Photochemical reactivity of siderophores produced by marine heterotrophic bacteria and cyanobacteria based on characteristic Fe(III) binding groups

Barbeau, K. A., Rue, E. L., Trick, C. G., Bruland, K. W., & Butler, A. (2003) · Limnology and Oceanography · doi:10.4319/lo.2003.48.3.1069 · Cited by 254 · see citing works

Molecular Underpinnings of Fe(III) Oxide Reduction by Shewanella Oneidensis MR-1

Shi, L., Rosso, K. M., Clarke, T. A., et al. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00050 · Cited by 243 · see citing works

Comparative genomics of freshwater Fe-oxidizing bacteria: implications for physiology, ecology, and systematics

Emerson, D., Field, E. K., Chertkov, O., Davenport, K. W., Goodwin, L., Munk, C. A., Nolan, M., & Woyke, T. (2013) · Frontiers in Microbiology · doi:10.3389/fmicb.2013.00254 · Cited by 235 · see citing works

The pio Operon Is Essential for Phototrophic Fe(II) Oxidation in Rhodopseudomonas palustris TIE-1

Jiao, Y., & Newman, D. K. (2006) · Journal of Bacteriology · doi:10.1128/jb.00776-06 · Cited by 230 · see citing works

Potential Role of Nitrite for Abiotic Fe(II) Oxidation and Cell Encrustation during Nitrate Reduction by Denitrifying Bacteria

Klueglein, N., Zeitvogel, F., Stierhof, Y., Floetenmeyer, M., Konhauser, K. O., Kappler, A. A., & Obst, M. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.03277-13 · Cited by 228 · see citing works

Humic Acid Reduction by Propionibacterium freudenreichii and Other Fermenting Bacteria

Benz, M., Schink, B., & Brune, A. (1998) · Applied and Environmental Microbiology · doi:10.1128/aem.64.11.4507-4512.1998 · Cited by 226 · see citing works

Low-oxygen and chemical kinetic constraints on the geochemical niche of neutrophilic iron(II) oxidizing microorganisms

Druschel, G. K., Emerson, D., Sutka, R. L., Suchecki, P., & Luther, G. W. (2008) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2008.04.035 · Cited by 225 · see citing works

Rapid electron exchange between surface-exposed bacterial cytochromes and Fe(III) minerals

White, G. F., Shi, Z., Shi, L., Wang, Z.-M., Dohnalkova, A. C., Marshall, M. J., Fredrickson, J. K., Zachara, J. M., Butt, J. N., Richardson, D. J., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1220074110 · Cited by 220 · see citing works

Composition and structural aspects of naturally occurring ferrihydrite

Cismasu, A. C., Michel, F. M., Tcaciuc, A. P., Tyliszczak, T., & Brown, G. E. (2011) · Comptes Rendus Géoscience · doi:10.1016/j.crte.2010.11.001 · Cited by 219 · see citing works

Isolation and Characterization of a Genetically Tractable Photoautotrophic Fe(II)-Oxidizing Bacterium, Rhodopseudomonas palustris Strain TIE-1

Jiao, Y., Kappler, A. A., Croal, L. R., & Newman, D. K. (2005) · Applied and Environmental Microbiology · doi:10.1128/aem.71.8.4487-4496.2005 · Cited by 219 · see citing works

Chlorobium ferrooxidans sp. nov., a phototrophic green sulfur bacterium that oxidizes ferrous iron in coculture with a "Geospirillum" sp. strain

Heising, S., Richter, L., Ludwig, W., & Schink, B. (1999) · Archives of Microbiology · doi:10.1007/s002030050748 · Cited by 218 · see citing works

Evolution of electron transfer out of the cell: comparative genomics of six Geobacter genomes

Butler, J. E., Young, N. D., & Lovley, D. R. (2010) · BMC Genomics · doi:10.1186/1471-2164-11-40 · Cited by 214 · see citing works

A novel metatranscriptomic approach to identify gene expression dynamics during extracellular electron transfer

Ishii, S., Suzuki, S., Norden‐Krichmar, T. M., Tenney, A. E., Chain, P., Scholz, M. B., Nealson, K. H., & Bretschger, O. (2013) · Nature Communications · doi:10.1038/ncomms2615 · Cited by 205 · see citing works

Identification and Characterization of MtoA: A Decaheme c-Type Cytochrome of the Neutrophilic Fe(II)-Oxidizing Bacterium Sideroxydans lithotrophicus ES-1

Liu, J., Wang, Z.-M., Belchik, S. M., et al. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00037 · Cited by 204 · see citing works

Concentration of Mn and separation from Fe in sediments—I. Kinetics and stoichiometry of the reaction between birnessite and dissolved Fe(II) at 10°C

Postma, D. (1985) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(85)90316-3 · Cited by 199 · see citing works

Characterization of Neutrophilic Fe(II)-Oxidizing Bacteria Isolated from the Rhizosphere of Wetland Plants and Description ofFerritrophicum radicicolagen. nov. sp. nov., andSideroxydans paludicolasp. nov.

Weiss, J. V., Rentz, J. A., Plaia, T. W., Neubauer, S. C., Merrill-Floyd, M., Lilburn, T., Bradburne, C. E., Megonigal, J. P., & Emerson, D. (2007) · Geomicrobiology Journal · doi:10.1080/01490450701670152 · Cited by 198 · see citing works

Transcriptomic and Genetic Analysis of Direct Interspecies Electron Transfer

Shrestha, P. M., Rotaru, A., Summers, Z. M., Shrestha, M., Liu, F., & Lovley, D. R. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.03837-12 · Cited by 193 · see citing works

Repeated Anaerobic Microbial Redox Cycling of Iron

Coby, A. J., Picardal, F. W., Shelobolina, E. S., Xu, H., & Roden, E. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.00276-11 · Cited by 185 · see citing works

Ecophysiology and the energetic benefit of mixotrophic Fe(II) oxidation by various strains of nitrate-reducing bacteria

Muehe, E. M., Gerhardt, S., Schink, B., & Kappler, A. A. (2009) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2009.00755.x · Cited by 181 · see citing works

Reduction of Organically Complexed Ferric Iron by Superoxide in a Simulated Natural Water

Rose, A. L., & Waite, T. D. (2005) · Environmental Science & Technology · doi:10.1021/es048765k · Cited by 179 · see citing works

Biochemical characterization of purified OmcS, a c-type cytochrome required for insoluble Fe(III) reduction in Geobacter sulfurreducens

Qian, X., Mester, T., Morgado, L., Arakawa, T., Sharma, M. L., Inoue, K., Joseph, C. A., Salgueiro, C. A., Maroney, M. J., & Lovley, D. R. (2011) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2011.01.003 · Cited by 179 · see citing works

Light penetration and light intensity in sandy marine sediments measured with irradiance and scalar irradiance fiber-optic microprobes

Kuhl, M. E., Lassen, C., & Jørgensen, B. B. (1994) · Marine Ecology Progress Series · doi:10.3354/meps105139 · Cited by 177 · see citing works

Photochemistry of Organic Iron(III) Complexing Ligands in Oceanic Systems

Barbeau, K. A. (2006) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.2006.tb09806.x · Cited by 176 · see citing works

Abiotic and Microbial Interactions during Anaerobic Transformations of Fe(II) and NOX-

Picardal, F. W. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00112 · Cited by 175 · see citing works

Anaerobic, Nitrate-Dependent Oxidation of Pyrite Nanoparticles by Thiobacillus denitrificans

Bosch, J., Lee, K., Jordan, G., Kim, K., & Meckenstock, R. U. (2011) · Environmental Science & Technology · doi:10.1021/es2022329 · Cited by 174 · see citing works

Extracellular Iron Biomineralization by Photoautotrophic Iron-Oxidizing Bacteria

Miot, J., Benzerara, K., Obst, M., Kappler, A. A., Hegler, F., Schädler, S., Bouchez, C., Guyot, F., & Morin, G. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.00490-09 · Cited by 173 · see citing works

Iron reduction by photoproduced superoxide in seawater

Voelker, B. M., & Sedlak, D. L. (1995) · Marine Chemistry · doi:10.1016/0304-4203(95)00029-q · Cited by 173 · see citing works

Periplasmic Electron Transfer via the c -Type Cytochromes MtrA and FccA of Shewanella oneidensis MR-1

Schuetz, B., Schicklberger, M., Kuermann, J., et al. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01834-09 · Cited by 169 · see citing works

Superoxide production by marine microalgae

Marshall, J.-A., de Salas, M. F., Oda, T., & Hallegraeff, G. M. (2005) · Marine Biology · doi:10.1007/s00227-005-1596-7 · Cited by 168 · see citing works

Enhanced Growth of Acidovorax sp. Strain 2AN during Nitrate-Dependent Fe(II) Oxidation in Batch and Continuous-Flow Systems

Chakraborty, A., Roden, E., Schieber, J., et al. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.06214-11 · Cited by 168 · see citing works

Dissimilatory Fe(III) and Mn(IV) Reduction by Shewanella putrefaciens Requires ferE , a Homolog of the pulE ( gspE ) Type II Protein Secretion Gene

DiChristina, T. J., Moore, C. M., & Haller, C. A. (2002) · Journal of Bacteriology · doi:10.1128/jb.184.1.142-151.2002 · Cited by 159 · see citing works

Reduction of humic substances by halorespiring, sulphate‐reducing and methanogenic microorganisms

Cervantes, F. J., de Bok, F. A. M., Duong‐Dac, T., Stams, A. J. M., Lettinga, G., & Field, J. A. (2002) · Environmental Microbiology · doi:10.1046/j.1462-2920.2002.00258.x · Cited by 155 · see citing works

Photochemistry of Organic Iron(III) Complexing Ligands in Oceanic Systems

Barbeau, K. A. (2006) · Photochemistry and Photobiology · doi:10.1562/2006-06-16-ir-935 · Cited by 153 · see citing works

Light‐induced redox cycling of iron in circumneutral lakes

Emmenegger, L., Schönenberger, R., Sigg, L., et al. (2001) · Limnology and Oceanography · doi:10.4319/lo.2001.46.1.0049 · Cited by 151 · see citing works

Stimulation by lepidocrocite (7-FeOOH) of Fe(II)-dependent nitrite reduction

Sørensen, J., & Thorling, L. (1991) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(91)90307-q · Cited by 150 · see citing works

Mariprofundus ferrooxydans PV-1 the First Genome of a Marine Fe(II) Oxidizing Zetaproteobacterium

Singer, E., Emerson, D., Webb, E. A., Barco, R. A., Kuenen, J. G., Nelson, W. C., Chan, C. S., Comolli, L. R., Ferriera, S., Johnson, J. H., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025386 · Cited by 147 · see citing works

Use of Superoxide as an Electron Shuttle for Iron Acquisition by the Marine Cyanobacterium Lyngbya majuscula

Rose, A. L., Salmon, T. P., Lukondeh, T., Neilan, B. A., & Waite, T. D. (2005) · Environmental Science & Technology · doi:10.1021/es048766c · Cited by 146 · see citing works

Electron flow through proteins

Gray, H. B., & Winkler, J. R. (2009) · Chemical Physics Letters · doi:10.1016/j.cplett.2009.10.051 · Cited by 145 · see citing works

A SELECTIVE ENRICHMENT METHOD FOR GALLIONELLA FERRUGINEA

Kucera, S., & WOLFE, R. S. (1957) · Journal of Bacteriology · doi:10.1128/jb.74.3.344-349.1957 · Cited by 142 · see citing works

Use of Fe(III) as an Electron Acceptor To Recover Previously Uncultured Hyperthermophiles: Isolation and Characterization of Geothermobacterium ferrireducens gen. nov., sp. nov

Kashefi, K., Holmes, D. E., Reysenbach, A., & Lovley, D. R. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.4.1735-1742.2002 · Cited by 136 · see citing works

Composition and Activity of an Autotrophic Fe(II)-Oxidizing, Nitrate-Reducing Enrichment Culture

Blöthe, M., & Roden, E. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01742-09 · Cited by 133 · see citing works

Oxidation of Ammonium to Nitrite Under Iron-Reducing Conditions in Wetland Soils

Shrestha, J., Rich, J. J., Ehrenfeld, J. G., et al. (2009) · Soil Science · doi:10.1097/ss.0b013e3181988fbf · Cited by 127 · see citing works

Anaerobic Benzene Oxidation via Phenol in Geobacter metallireducens

Zhang, T., Tremblay, P., Chaurasia, A. K., et al. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.03134-13 · Cited by 123 · see citing works

Toward a Mechanistic Understanding of Anaerobic Nitrate-Dependent Iron Oxidation: Balancing Electron Uptake and Detoxification

Carlson, H. K., Clark, I. C., Melnyk, R. A., & Coates, J. D. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00057 · Cited by 120 · see citing works

Induction of Nitrate-Dependent Fe(II) Oxidation by Fe(II) in Dechloromonas sp. Strain UWNR4 and Acidovorax sp. Strain 2AN

Chakraborty, A., & Picardal, F. W. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.02709-12 · Cited by 116 · see citing works

Iron Sulfide and Pyrite as Potential Electron Donors for Microbial Nitrate Reduction in Freshwater Wetlands

Haaijer, S. C. M., Lamers, L. P. M., Smolders, A. J. P., Jetten, M. S. M., & den Camp, H. J. M. O. (2007) · Geomicrobiology Journal · doi:10.1080/01490450701436489 · Cited by 110 · see citing works

Control of Ferrous Iron Oxidation within Circumneutral Microbial Iron Mats by Cellular Activity and Autocatalysis

Rentz, J. A., Kraiya, C., Luther, G. W., & Emerson, D. (2007) · Environmental Science & Technology · doi:10.1021/es062203e · Cited by 109 · see citing works

Nonlocal bacterial electron transfer to hematite surfaces

Rosso, K. M., Zachara, J. M., Fredrickson, J. K., Gorby, Y. A., & Smith, S. C. (2003) · Geochimica et Cosmochimica Acta · doi:10.1016/s0016-7037(02)00904-3 · Cited by 109 · see citing works

Antibody Recognition Force Microscopy Shows that Outer Membrane Cytochromes OmcA and MtrC Are Expressed on the Exterior Surface of Shewanella oneidensis MR-1

Lower, B. H., Yongsunthon, R., Shi, L., et al. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.02108-08 · Cited by 107 · see citing works

Effect of nitrate on reduction of ferric iron by a bacterium isolated from crude oil

Obuekwe, C. O., Westlake, D. W. S., & Cook, F. D. (1981) · Canadian Journal of Microbiology · doi:10.1139/m81-107 · Cited by 106 · see citing works

Charge transfer spectra of transition metal complexes

Lever, A. B. P. (1974) · Journal of Chemical Education · doi:10.1021/ed051p612 · Cited by 103 · see citing works

Physiological and taxonomic description of the novel autotrophic, metal oxidizing bacterium, Pseudogulbenkiania sp. strain 2002

Weber, K. A., Hedrick, D. B., Peacock, A. D., Thrash, J. C., White, D. C., Achenbach, L. A., & Coates, J. D. (2009) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-009-1934-7 · Cited by 103 · see citing works

The fox Operon from Rhodobacter Strain SW2 Promotes Phototrophic Fe(II) Oxidation in Rhodobacter capsulatus SB1003

Croal, L. R., Jiao, Y., & Newman, D. K. (2006) · Journal of Bacteriology · doi:10.1128/jb.01395-06 · Cited by 100 · see citing works

What's New Is Old: Resolving the Identity of Leptothrix ochracea Using Single Cell Genomics, Pyrosequencing and FISH

Fleming, E. J., Langdon, A. E., Martínez‐García, M., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017769 · Cited by 99 · see citing works

Role of outer‐membrane cytochromes MtrC and OmcA in the biomineralization of ferrihydrite by Shewanella oneidensis MR‐1

Reardon, C. L., Dohnalkova, A. C., Nachimuthu, P., Kennedy, D. W., Saffarini, D. A., Arey, B. W., SHI, L., Wang, Z., MOORE, D., McLean, J. S., et al. (2009) · Geobiology · doi:10.1111/j.1472-4669.2009.00226.x · Cited by 94 · see citing works

Mineralogy of Iron Microbial Mats from Loihi Seamount

Toner, B. M., Berquó, T. S., Michel, F. M., Sorensen, J. V., Templeton, A. S., & Edwards, K. J. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00118 · Cited by 93 · see citing works

Biochemical and genetic evidence of benzylsuccinate synthase intoluene-degrading, ferric iron-reducing Geobacter metallireducens

Kane, S. R., Beller, H. R., Legler, T. C., et al. (2002) · Biodegradation · doi:10.1023/a:1020454831407 · Cited by 90 · see citing works

Persistence of iron(II) in surface waters of the western subarctic Pacific

Roy, E. G., Wells, M. L., & King, D. W. (2008) · Limnology and Oceanography · doi:10.4319/lo.2008.53.1.0089 · Cited by 90 · see citing works

Sulfur Species as Redox Partners and Electron Shuttles for Ferrihydrite Reduction by Sulfurospirillum deleyianum

Lohmayer, R., Kappler, A. A., Lösekann, T., & Planer‐Friedrich, B. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.04220-13 · Cited by 89 · see citing works

Role of extracellular peroxidase in the superoxide production by wheat root cells

Minibayeva, F. V., Gordon, L. K., Kolesnikov, O. P., et al. (2001) · PROTOPLASMA · doi:10.1007/bf01289421 · Cited by 88 · see citing works

Anaerobic degradation of aromatic compounds coupled to Fe(III) reduction by Ferroglobus placidus

Tor, J. M., & Lovley, D. R. (2001) · Environmental Microbiology · doi:10.1046/j.1462-2920.2001.00192.x · Cited by 87 · see citing works

Does a low-pH microenvironment around phototrophic FeII-oxidizing bacteria prevent cell encrustation by FeIII minerals?

Hegler, F., Schmidt, C., Schwarz, H., & Kappler, A. A. (2010) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2010.00975.x · Cited by 82 · see citing works

The Influence of Extracellular Superoxide on Iron Redox Chemistry and Bioavailability to Aquatic Microorganisms

Rose, A. L. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00124 · Cited by 82 · see citing works

FeII oxidation by molecular O2 during HCl extraction

Porsch, K., & Kappler, A. A. (2011) · Environmental Chemistry · doi:10.1071/en10125 · Cited by 76 · see citing works

" Genome-enabled studies of anaerobic, nitrate-dependent iron oxidation in the chemolithoautotrophic bacterium Thiobacillus denitrificans"

Beller, H. R., Zhou, P., Legler, T. C., et al. (2013) · Frontiers in Microbiology · doi:10.3389/fmicb.2013.00249 · Cited by 75 · see citing works

A novel Geobacteraceae-specific outer membrane protein J (OmpJ) is essential for electron transport to Fe (III) and Mn (IV) oxides in Geobacter sulfurreducens

Afkar, E., Reguera, G., Schiffer, M., & Lovley, D. R. (2005) · BMC Microbiology · doi:10.1186/1471-2180-5-41 · Cited by 73 · see citing works

Hidden in plain sight: discovery of sheath-forming, iron-oxidizing<i>Zetaproteobacteria</i>at Loihi Seamount, Hawaii, USA

Fleming, E. J., Davis, R. E., McAllister, S. M., Chan, C. S., Moyer, C. L., Tebo, B. M., & Emerson, D. (2013) · FEMS Microbiology Ecology · doi:10.1111/1574-6941.12104 · Cited by 72 · see citing works

Vorläufige Mittheilungen über das wirkliche Vorkommen fossiler Infusorien und ihre grosse Verbreitung

Ehrenberg (1836) · Annalen der Physik · doi:10.1002/andp.18361140520 · Cited by 71 · see citing works

Influence of Seasonal and Geochemical Changes on the Geomicrobiology of an Iron Carbonate Mineral Water Spring

Hegler, F., Lösekann, T., Hanselmann, K. W., Behrens, S., & Kappler, A. A. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.01440-12 · Cited by 63 · see citing works

Microbial Iron(II) Oxidation in Littoral Freshwater Lake Sediment: The Potential for Competition between Phototrophic vs. Nitrate-Reducing Iron(II)-Oxidizers

Melton, E. D., Schmidt, C., & Kappler, A. A. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00197 · Cited by 60 · see citing works

Dark production of hydrogen peroxide in the Gulf of Alaska

Vermilyea, A. W., Hansard, S. P., & Voelker, B. M. (2010) · Limnology and Oceanography · doi:10.4319/lo.2010.55.2.0580 · Cited by 60 · see citing works

Competition Between O2 and H2O2 in the Oxidation of Fe(II) in Natural Waters

González‐Dávila, M., Santana‐Casiano, J. M., & Millero, F. J. (2006) · Journal of Solution Chemistry · doi:10.1007/s10953-006-8942-3 · Cited by 54 · see citing works

Impact of natural organic matter on H2O2-mediated oxidation of Fe(II) in a simulated freshwater system

Miller, C. J., Rose, A. L., & Waite, T. D. (2009) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2009.02.027 · Cited by 53 · see citing works

Iron: The Forgotten Driver of Nitrous Oxide Production in Agricultural Soil

Zhu‐Barker, X., Silva, L. C. R., Doane, T. A., & Horwáth, W. R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060146 · Cited by 49 · see citing works

Biogeochemistry and microbiology of microaerobic Fe(II) oxidation

Emerson, D. (2012) · Biochemical Society Transactions · doi:10.1042/bst20120154 · Cited by 49 · see citing works

Near‐neutral surface charge and hydrophilicity prevent mineral encrustation of F e‐oxidizing micro‐organisms

Saini, G., & Chan, C. S. (2012) · Geobiology · doi:10.1111/gbi.12021 · Cited by 48 · see citing works

Effects of temperature on rates and mineral products of microbial Fe(II) oxidation by Leptothrix cholodnii at microaerobic conditions

Vollrath, S., Behrends, T., Koch, C., & Cappellen, P. V. (2013) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2013.01.019 · Cited by 46 · see citing works

Phototrophic Fe(II) oxidation in an atmosphere of H2: implications for Archean banded iron formations

Croal, L. R., Jiao, Y., Kappler, A. A., & Newman, D. K. (2008) · Geobiology · doi:10.1111/j.1472-4669.2008.00185.x · Cited by 38 · see citing works

Functional Characterization of the FoxE Iron Oxidoreductase from the Photoferrotroph Rhodobacter ferrooxidans SW2

Saraiva, I. H., Newman, D. K., & Louro, R. O. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.360636 · Cited by 31 · see citing works

The c -Type Cytochrome OmcA Localizes to the Outer Membrane upon Heterologous Expression in Escherichia coli

Donald, J. W., Hicks, M. G., Richardson, D. J., et al. (2008) · Journal of Bacteriology · doi:10.1128/jb.00395-08 · Cited by 28 · see citing works

Albidoferax, a new genus of Comamonadaceae and reclassification of Rhodoferax ferrireducens (Finneran et al., 2003) as Albidoferax ferrireducens comb. nov.

Ramana, C. V., & Sasikala, C. (2009) · The Journal of General and Applied Microbiology · doi:10.2323/jgam.55.301 · Cited by 25 · see citing works

Metabolic Flexibility and Substrate Preference by the Fe(II)-Oxidizing Purple Non-Sulphur BacteriumRhodopseudomonas palustrisStrain TIE-1

Melton, E. D., Schmidt, C., Behrens, S., Schink, B., & Kappler, A. A. (2014) · Geomicrobiology Journal · doi:10.1080/01490451.2014.901439 · Cited by 25 · see citing works

Comparison of Humic Substance- and Fe(III)-Reducing Microbial Communities in Anoxic Aquifers

Piepenbrock, A., Behrens, S., & Kappler, A. A. (2014) · Geomicrobiology Journal · doi:10.1080/01490451.2014.911994 · Cited by 19 · see citing works

Biotic and abiotic controls on iron oxyhydroxide formation in the gill chamber of the hydrothermal vent shrimp Rimicaris exoculata

Schmidt, C., Corbari, L., Gaill, F., & Bris, N. L. (2009) · Geobiology · doi:10.1111/j.1472-4669.2009.00209.x · Cited by 18 · see citing works

Photomixotrophic growth of Rhodobacter capsulatus SB1003 on ferrous iron

Kopf, S., & Newman, D. K. (2011) · Geobiology · doi:10.1111/j.1472-4669.2011.00313.x · Cited by 17 · see citing works

ChemInform Abstract: Pulse Radiolytic Studies of the Reactions of HO2/O2‐ with Fe(II)/Fe(III) Ions.

Rush, J. D., & Bielski, B. H. J. (1986) · ChemInform · doi:10.1002/chin.198608032 · Cited by 10 · see citing works

Rapid electron transfer by the carbon matrix in natural pyrogenic carbon

Sun, T., Levin, B. D. A., Guzman, J. J. L., Enders, A., Muller, D. A., Angenent, L. T., & Lehmann, J. (2017) · Nature Communications · doi:10.1038/ncomms14873 · Cited by 626 · see citing works

Microbially catalyzed dolomite formation: From near-surface to burial

Petrash, D. A., Bialik, O. M., Bontognali, T. R. R., Vasconcelos, C., Roberts, J. A., McKenzie, J. A., & Konhauser, K. O. (2017) · Earth-Science Reviews · doi:10.1016/j.earscirev.2017.06.015 · Cited by 338 · see citing works

Sustainable remediation with an electroactive biochar system: mechanisms and perspectives

Wan, Z., Sun, Y., Tsang, D. C. W., Hou, D., Cao, X., Zhang, S., Gao, B., & Ok, Y. S. (2020) · Green Chemistry · doi:10.1039/d0gc00717j · Cited by 162 · see citing works

Cropping With Slag to Address Soil, Environment, and Food Security

Das, S., Kim, G. W., Hwang, H. Y., Verma, P. P., & Kim, P. J. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01320 · Cited by 107 · see citing works

The Laurentian Great Lakes: A Biogeochemical Test Bed

Sterner, R. W. (2020) · Annual Review of Earth and Planetary Sciences · doi:10.1146/annurev-earth-071420-051746 · Cited by 35 · see citing works

Biogeochemical cycles of elements

Sigel, A., Sigel, H., & Sigel, R. K. O. (2005) · Cited by 25 · see citing works

Biogeochemistry

Ranaweera, D., Kumarasinghe, U., Senanayake, C. M., Dassanayake, R. S., Bandara, P. C., & Koliyabandara, P. A. (2023) · doi:10.1002/9781119867371.ch2 · Cited by 7 · see citing works

Linking biogeochemical processes to microbial communities in permeable sediments

Chen, Y.-J. (2020) · Figshare · doi:10.26180/5eedc87087d94

The importance of time and space in biogeochemical heterogeneity and processing along the reservoir ecosystem continuum

Woelmer, W. M., Hounshell, A. G., Lofton, M. E., et al. (2023) · Aquatic Sciences · doi:10.1007/s00027-023-00959-7 · Cited by 14 · see citing works