Works by Hoehler, Tori
Results: 33
Microbiology: Hydrogen for dinner.
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- Nature, 2011, v. 476, n. 7359, p. 154, doi. 10.1038/476154a
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Accessing the Subsurface Biosphere Within Rocks Undergoing Active Low‐Temperature Serpentinization in the Samail Ophiolite (Oman Drilling Project).
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- Journal of Geophysical Research. Biogeosciences, 2021, v. 126, n. 10, p. 1, doi. 10.1029/2021JG006315
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Biogeochemical Gradients in a Serpentinization‐Influenced Aquifer: Implications for Gas Exchange Between the Subsurface and Atmosphere.
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- Journal of Geophysical Research. Biogeosciences, 2021, v. 126, n. 8, p. 1, doi. 10.1029/2020JG006209
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Geochemical bioenergetics during low-temperature serpentinization: An example from the Samail ophiolite, Sultanate of Oman.
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- Journal of Geophysical Research. Biogeosciences, 2017, v. 122, n. 7, p. 1821, doi. 10.1002/2017JG003825
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Biogeochemistry: Methane minimalism.
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- Nature, 2014, v. 507, n. 7493, p. 436, doi. 10.1038/nature13215
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LEVERAGING EARTH HYDROSPHERE SCIENCE IN THE SEARCH FOR LIFE ON OCEAN WORLDS.
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- Oceanography, 2022, v. 35, n. 1, p. 74, doi. 10.5670/oceanog.2021.412
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OCEAN SYSTEM SCIENCE TO INFORM THE EXPLORATION OF OCEAN WORLDS.
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- Oceanography, 2022, v. 35, n. 1, p. 47, doi. 10.5670/oceanog.2021.411
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Geophysical Characterization of Serpentinite Hosted Hydrogeology at the McLaughlin Natural Reserve, Coast Range Ophiolite.
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- Geochemistry, Geophysics, Geosystems: G3, 2018, v. 19, n. 1, p. 114, doi. 10.1002/2017GC007001
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Serpentinization-Influenced Groundwater Harbors Extremely Low Diversity Microbial Communities Adapted to High pH.
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- Frontiers in Microbiology, 2017, v. 8, p. 1, doi. 10.3389/fmicb.2017.00308
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Drivers of Bacterial Maintenance and Minimal Energy Requirements.
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- Frontiers in Microbiology, 2017, v. 7/8, p. 1, doi. 10.3389/fmicb.2017.00031
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Microsensor measurements of hydrogen gas dynamics in cyanobacterial microbial mats.
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- Frontiers in Microbiology, 2015, p. 1, doi. 10.3389/fmicb.2015.00726
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Insights into environmental controls on microbial communities in a continental serpentinite aquifer using a microcosm-based approach.
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- Frontiers in Microbiology, 2014, v. 5, p. 1, doi. 10.3389/fmicb.2014.00604
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Acetogenesis from CO<sub>2</sub> in an anoxic marine sediment.
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- Limnology & Oceanography, 1999, v. 44, n. 3, p. 662, doi. 10.4319/lo.1999.44.3.0662
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Microbial life under extreme energy limitation.
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- Nature Reviews Microbiology, 2013, v. 11, n. 2, p. 83, doi. 10.1038/nrmicro2939
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Modeled energetics of bacterial communities in ancient subzero brines.
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- Frontiers in Microbiology, 2023, p. 1, doi. 10.3389/fmicb.2023.1206641
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A dynamic microbial sulfur cycle in a serpentinizing continental ophiolite.
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- Environmental Microbiology, 2020, v. 22, n. 6, p. 2329, doi. 10.1111/1462-2920.15006
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Probing the geological source and biological fate of hydrogen in Yellowstone hot springs.
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- Environmental Microbiology, 2019, v. 21, n. 10, p. 3816, doi. 10.1111/1462-2920.14730
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Competition for inorganic carbon between oxygenic and anoxygenic phototrophs in a hypersaline microbial mat, Guerrero Negro, Mexico.
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- Environmental Microbiology, 2013, v. 15, n. 5, p. 1532, doi. 10.1111/1462-2920.12032
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Hydrogen ‘leakage’ during methanogenesis from methanol and methylamine: implications for anaerobic carbon degradation pathways in aquatic sediments.
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- Environmental Microbiology, 2007, v. 9, n. 4, p. 1060, doi. 10.1111/j.1462-2920.2007.01248.x
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Phosphate availability and implications for life on ocean worlds.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37770-9
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Field and laboratory studies of methane oxidation in an anoxic marine sediment: Evidence for a methanogen-sulfate reducer consortium.
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- Global Biogeochemical Cycles, 1994, v. 8, n. 4, p. 451, doi. 10.1029/94GB01800
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Subsurface processes influence oxidant availability and chemoautotrophic hydrogen metabolism in Yellowstone hot springs.
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- Geobiology, 2018, v. 16, n. 6, p. 674, doi. 10.1111/gbi.12308
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Methane production by microbial mats under low sulphate concentrations.
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- Geobiology, 2004, v. 2, n. 2, p. 87, doi. 10.1111/j.1472-4677.2004.00024.x
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Modeled energetics of bacterial communities in ancient subzero brines.
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- Frontiers in Microbiology, 2024, p. 1, doi. 10.3389/fmicb.2023.1206641
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Editorial: Studies on life at the energetic edge – from laboratory experiments to field-based investigations, volume II.
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- Frontiers in Microbiology, 2024, p. 1, doi. 10.3389/fmicb.2023.1351761
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Formation of mixed-layer sulfide-hydroxide minerals from the Tochilinite-Valleriite group during experimental serpentinization of olivine.
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- American Mineralogist, 2024, v. 109, n. 1, p. 61, doi. 10.2138/am-2022-8625
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Evolutionary tradeoffs in cellular composition across diverse bacteria.
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- ISME Journal: Multidisciplinary Journal of Microbial Ecology, 2016, v. 10, n. 9, p. 2145, doi. 10.1038/ismej.2016.21
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Revisiting N<sub>2</sub> fixation in Guerrero Negro intertidal microbial mats with a functional single-cell approach.
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- ISME Journal: Multidisciplinary Journal of Microbial Ecology, 2015, v. 9, n. 2, p. 485, doi. 10.1038/ismej.2014.144
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Anoxic carbon flux in photosynthetic microbial mats as revealed by metatranscriptomics.
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- ISME Journal: Multidisciplinary Journal of Microbial Ecology, 2013, v. 7, n. 4, p. 817, doi. 10.1038/ismej.2012.150
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Identification of a novel cyanobacterial group as active diazotrophs in a coastal microbial mat using NanoSIMS analysis.
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- ISME Journal: Multidisciplinary Journal of Microbial Ecology, 2012, v. 6, n. 7, p. 1427, doi. 10.1038/ismej.2011.200
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Hydrogen production in photosynthetic microbial mats in the Elkhorn Slough estuary, Monterey Bay.
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- ISME Journal: Multidisciplinary Journal of Microbial Ecology, 2012, v. 6, n. 4, p. 863, doi. 10.1038/ismej.2011.142
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The role of microbial mats in the production of reduced gasses on the early Earth.
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- Nature, 2001, v. 412, n. 6844, p. 324, doi. 10.1038/35085554
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Energetic and genomic potential for hydrogenotrophic, formatotrophic, and acetoclastic methanogenesis in surface-expressed serpentinized fluids of the Samail Ophiolite.
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- Frontiers in Microbiology, 2025, p. 1, doi. 10.3389/fmicb.2024.1523912
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