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A. Lasaga, A. Lüttge (2004)
Mineralogical approaches to fundamental crystal dissolution kineticsAmerican Mineralogist, 89
P. Bennett, F. Hiebert, J. Rogers (2000)
Microbial control of mineral–groundwater equilibria:Macroscale to microscaleHydrogeology Journal, 8
C. Myers, K. Nealson (1988)
Bacterial Manganese Reduction and Growth with Manganese Oxide as the Sole Electron AcceptorScience, 240
D. Newman, R. Kolter (2000)
A role for excreted quinones in extracellular electron transferNature, 405
R. Arvidson, Mikala Beig, A. Luttge (2004)
Single-crystal plagioclase feldspar dissolution rates measured by vertical scanning interferometryAmerican Mineralogist, 89
K. Nealson, C. Myers (1992)
Microbial reduction of manganese and iron: new approaches to carbon cyclingApplied and Environmental Microbiology, 58
D. Lovley, E. Phillips (1988)
Novel Mode of Microbial Energy Metabolism: Organic Carbon Oxidation Coupled to Dissimilatory Reduction of Iron or ManganeseApplied and Environmental Microbiology, 54
(2004)
Lüttge A (2004b) Mineralogical approaches to fundamental crystal dissolution kinetics – Dissolution of an A(3)B structure
(2003)
Lüttge A (2003) A model for crystal dissolution
(1996)
Adhesion as a strategy for access to nutrients
Peter Risthaus, D. Bosbach, U. Becker, A. Putnis (2001)
Barite scale formation and dissolution at high ionic strength studied with atomic force microscopyColloids and Surfaces A: Physicochemical and Engineering Aspects, 191
(2004)
The mechanistic consequences of microbial surface colonization on carbonate mineral dissolution
P. Bennett, F. Hiebert, Wan-joo Choi (1996)
Microbial colonization and weathering of silicates in a petroleum-contaminated groundwaterChemical Geology, 132
W. Barker, S. Welch, J. Banfield (1997)
Chapter 12. BIOGEOCHEMICAL WEATHERING OF SILICATE MINERALS
D. Lovley, J. Coates, E. Blunt-Harris, E. Phillips, J. Woodward (1996)
Humic substances as electron acceptors for microbial respirationNature, 382
A. Lasaga, A. Lüttge (2005)
Kinetic justification of the solubility product: application of a general kinetic dissolution model.The journal of physical chemistry. B, 109 4
S. Kjelleberg, M. Hermansson (1984)
Starvation-Induced Effects on Bacterial Surface CharacteristicsApplied and Environmental Microbiology, 48
A. Lttge, U. Winkler, A. Lasaga (2003)
Interferometric study of the dolomite dissolution: a new conceptual model for mineral dissolutionGeochimica et Cosmochimica Acta, 67
J. Tiedje (2002)
Shewanella—the environmentally versatile genomeNature Biotechnology, 20
(1933)
IV . The relationship of microorganisms to the decay of stone
(1997)
Biogeochemistry of silicate mineral weathering. In: Geomicrobiology: Interactions between Microbes and Minerals, Reviews in mineralogy) Society of America (eds Banfield JF, Nealson KH)
T. DiChristina, E. Delong (1994)
Isolation of anaerobic respiratory mutants of Shewannella putrefaciens and genetic analysis of mutants deficient in anaerobic growth on Fe3+Journal of Bacteriology, 176
R. Arvidson, I. Ertan, J. Amonette, A. Lüttge (2003)
Variation in Calcite Dissolution Rates: A Fundamental Problem?Geochimica et Cosmochimica Acta, 67
A. Lüttge, P. Conrad (2004)
Direct Observation of Microbial Inhibition of Calcite DissolutionApplied and Environmental Microbiology, 70
A. Gratz, P. Hillner, P. Hansma (1993)
Step dynamics and spiral growth on calciteGeochimica et Cosmochimica Acta, 57
H. Teng, P. Dove, J. Yoreo (2000)
Kinetics of calcite growth: Surface processes and relationships to macroscopic rate lawsGeochimica et Cosmochimica Acta, 64
Andreas Luettge, E. Bolton, A. Lasaga (1999)
An interferometric study of the dissolution kinetics of anorthite; the role of reactive surface areaAmerican Journal of Science, 299
M. Grantham, P. Dove (1996)
Investigation of bacterial-mineral interactions using Fluid Tapping Mode™ Atomic Force MicroscopyGeochimica et Cosmochimica Acta, 60
Yong Liang, D. Baer, J. McCoy, J. Amonette, J. Lafemina (1996)
Dissolution kinetics at the calcite-water interfaceGeochimica et Cosmochimica Acta, 60
A. Lasaga, A. Lüttge (2004)
Mineralogical approaches to fundamental crystal dissolution kinetics - Dissolution of an A3B structureEuropean Journal of Mineralogy, 16
Kasthuri Venkateswaran, Duane Moser, M. Dollhopf, D. Lies, D. Saffarini, Barbara MacGregor, D. Ringelberg, D. White, M. Nishijima, Hiroshi Sano, J. Burghardt, E. Stackebrandt, K. Nealson (1999)
Polyphasic taxonomy of the genus Shewanella and description of Shewanella oneidensis sp. nov.International journal of systematic bacteriology, 49 Pt 2
A. Lüttge, L. Zhang, K. Nealson (2003)
Mineral surfaces and their implications for microbial attachment: Results from Monte Carlo simulations and direct surface observationsAmerican Journal of Science, 305
H. Ehrlich (1998)
GEOMICROBIOLOGY: ITS SIGNIFICANCE FOR GEOLOGYEarth-Science Reviews, 45
(1997)
Biogeochemistry of silicate mineral weathering
K. Davis, P. Dove, J. Yoreo (2000)
The role of Mg2+ as an impurity in calcite growth.Science, 290 5494
D. Lovley, E. Blunt-Harris (1999)
Role of Humic-Bound Iron as an Electron Transfer Agent in Dissimilatory Fe(III) ReductionApplied and Environmental Microbiology, 65
C. Pina, U. Becker, Peter Risthaus, D. Bosbach, A. Putnis (1998)
Molecular-scale mechanisms of crystal growth in bariteNature, 395
S. Higgins, D. Bosbach, C. Eggleston, K. Knauss (2000)
Kink Dynamics and Step Growth on Barium Sulfate (001): A Hydrothermal Scanning Probe Microscopy StudyJournal of Physical Chemistry B, 104
J. Morse, F. Mackenzie (1990)
Geochemistry of Sedimentary Carbonates
S. Paine, F. Linggood, F. Schimmer, T. Thrupp (1932)
The Relationship of Micro-Organisms to the Decay of StonePhilosophical Transactions of the Royal Society B, 222
H. Teng, P. Dove, C. Orme, J. Yoreo (1998)
Thermodynamics of calcite growth: baseline for understanding biomineral formationScience, 282 5389
M. Dawson, B. Humphrey, K. Marshall (1981)
Adhesion: A tactic in the survival strategy of a marine vibrio during starvationCurrent Microbiology, 6
K. Davis, A. Lüttge (2005)
Quantifying the relationship between microbial attachment and mineral surface dynamics using vertical scanning interferometry (VSI)American Journal of Science, 305
A. Lasaga, A. Luttge (2001)
Variation of Crystal Dissolution Rate Based on a Dissolution Stepwave ModelScience, 291
(1996)
Microbial colonization and weathering of silicates in a petroleum-contaminated aquifer
Guntram Jordan, W. Rammensee (1998)
Dissolution Rates of Calcite (104) Obtained by Scanning Force Microscopy: Microtopography-Based Dissolution Kinetics on Surfaces with Anisotropic Step VelocitiesGeochimica et Cosmochimica Acta, 62
R. Arnold, T. DiChristina, M. Hoffmann (1988)
Reductive dissolution of fe(III) oxides by Pseudomonas sp. 200Biotechnology and Bioengineering, 32
J. Morse, R. Arvidson (2002)
The dissolution kinetics of major sedimentary carbonate mineralsEarth-Science Reviews, 58
J. Morse (1983)
Chapter 7. The KINETICS of CALCIUM CARBONATE DISSOLUTION and PRECIPITATION
(1983)
The kinetics of calcium carbonate dissolution and precipitation. In: Carbonates: Mineralogy and Chemistry, (Reviews in Mineralogy) (ed
K. Rosso, J. Zachara, J. Fredrickson, Y. Gorby, Steven Smith (2003)
Nonlocal bacterial electron transfer to hematite surfacesGeochimica et Cosmochimica Acta, 67
A. Lasaga, A. Lüttge (2003)
A model for crystal dissolutionEuropean Journal of Mineralogy, 15
C. Zobell (1943)
The Effect of Solid Surfaces upon Bacterial ActivityJournal of Bacteriology, 46
ABSTRACT Although microbes have been shown to alter the dissolution rate of carbonate minerals, a mechanistic understanding of the consequences of microbial surface colonization on carbonate dissolution has yet to be achieved. Here we report the use of vertical scanning interferometry (VSI) to study the effect of Shewanella oneidensis MR‐1 surface colonization on the dissolution rates of calcite (CaCO3) and dolomite (CaMg(CO3)2) through qualitative analysis of etch pit development and quantitative measurements of surface‐normal dissolution rates. By quantifying and comparing the significant processes occurring at the microbe–mineral interface, the dominant mechanism of mineral dissolution during surface colonization was determined. MR‐1 attachment under aerobic conditions was found to influence carbonate dissolution through two distinct mechanistic pathways: (1) inhibition of carbonate dissolution through interference with etch pit development and (2) excavation of carbonate material at the cell–mineral interface during irreversible attachment to the mineral surface. The relative importance of these two competing effects was found to vary with the solubility of the carbonate mineral studied. For the faster‐dissolving calcite substrates, inhibition of dissolution by attachment and subsequent extracellular polysaccharide (EPS) production was the dominant effect associated with MR‐1 surface colonization. This interference with etch pit development resulted in a 40–70% decrease in the surface normal dissolution rate relative to cell‐free controls, depending primarily on the concentration of cells in solution. However, in the case of the slower‐dissolving dolomite substrates, carbonate material displaced during the entrenchment of cells on the surface far outweighed the abiotic dissolution rate. Therefore, during the initial stages of surface colonization, dolomite dissolution rates were actually enhanced by MR‐1 attachment. This study demonstrates the dynamic and competitive relationship between microbial surface colonization and mineral dissolution that may be expected to occur in natural environments.
Geobiology – Wiley
Published: Jun 1, 2007
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