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      Abiotic methane formation during experimental serpentinization of olivine

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          Significance

          Abiotic methane discharged from serpentinizing rocks supplies metabolic energy to chemosynthetic microbial communities and may have done so since the earliest lifeforms evolved on Earth. Several recent reports have claimed observation of abiotic formation of methane during low-temperature serpentinization of olivine-rich rocks during laboratory experiments. However, using 13C-labeled carbon sources, this study shows that the methane observed in such experiments is predominantly derived from background sources rather than abiotic synthesis. Conversely, more rapid production of methane is observed when an H 2-rich vapor phase is present within the reaction vessel. Overall, the results indicate that in situ abiotic synthesis may contribute less methane to near-surface serpentinites than some recent studies have suggested.

          Abstract

          Fluids circulating through actively serpentinizing systems are often highly enriched in methane (CH 4). In many cases, the CH 4 in these fluids is thought to derive from abiotic reduction of inorganic carbon, but the conditions under which this process can occur in natural systems remain unclear. In recent years, several studies have reported abiotic formation of CH 4 during experimental serpentinization of olivine at temperatures at or below 200 °C. However, these results seem to contradict studies conducted at higher temperatures (300 °C to 400 °C), where substantial kinetic barriers to CH 4 synthesis have been observed. Here, the potential for abiotic formation of CH 4 from dissolved inorganic carbon during olivine serpentinization is reevaluated in a series of laboratory experiments conducted at 200 °C to 320 °C. A 13C-labeled inorganic carbon source was used to unambiguously determine the origin of CH 4 generated in the experiments. Consistent with previous high-temperature studies, the results indicate that abiotic formation of CH 4 from reduction of dissolved inorganic carbon during the experiments is extremely limited, with nearly all of the observed CH 4 derived from background sources. The results indicate that the potential for abiotic synthesis of CH 4 in low-temperature serpentinizing environments may be much more limited than some recent studies have suggested. However, more extensive production of CH 4 was observed in one experiment performed under conditions that allowed an H 2-rich vapor phase to form, suggesting that shallow serpentinization environments where a separate gas phase is present may be more favorable for abiotic synthesis of CH 4.

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          Most cited references38

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          SUPCRT92: A software package for calculating the standard molal thermodynamic properties of minerals, gases, aqueous species, and reactions from 1 to 5000 bar and 0 to 1000°C

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            Abiogenic hydrocarbon production at lost city hydrothermal field.

            Low-molecular-weight hydrocarbons in natural hydrothermal fluids have been attributed to abiogenic production by Fischer-Tropsch type (FTT) reactions, although clear evidence for such a process has been elusive. Here, we present concentration, and stable and radiocarbon isotope, data from hydrocarbons dissolved in hydrogen-rich fluids venting at the ultramafic-hosted Lost City Hydrothermal Field. A distinct "inverse" trend in the stable carbon and hydrogen isotopic composition of C1 to C4 hydrocarbons is compatible with FTT genesis. Radiocarbon evidence rules out seawater bicarbonate as the carbon source for FTT reactions, suggesting that a mantle-derived inorganic carbon source is leached from the host rocks. Our findings illustrate that the abiotic synthesis of hydrocarbons in nature may occur in the presence of ultramafic rocks, water, and moderate amounts of heat.
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              Abiogenic methane formation and isotopic fractionation under hydrothermal conditions

              Horita, Berndt (1999)
              Recently, methane (CH(4)) of possible abiogenic origin has been reported from many localities within Earth's crust. However, little is known about the mechanisms of abiogenic methane formation, or about isotopic fractionation during such processes. Here, a hydrothermally formed nickel-iron alloy was shown to catalyze the otherwise prohibitively slow formation of abiogenic CH(4) from dissolved bicarbonate (HCO(3)-) under hydrothermal conditions. Isotopic fractionation by the catalyst resulted in delta(13)C values of the CH(4) formed that are as low as those typically observed for microbial methane, with similarly high CH(4)/(C(2)H(6) + C(3)H(8)) ratios. These results, combined with the increasing recognition of nickel-iron alloy occurrence in oceanic crusts, suggest that abiogenic methane may be more widespread than previously thought.
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                Author and article information

                Journal
                Proc Natl Acad Sci U S A
                Proc. Natl. Acad. Sci. U.S.A
                pnas
                pnas
                PNAS
                Proceedings of the National Academy of Sciences of the United States of America
                National Academy of Sciences
                0027-8424
                1091-6490
                6 December 2016
                7 November 2016
                : 113
                : 49
                : 13965-13970
                Affiliations
                [1] aLaboratory for Atmospheric and Space Physics, University of Colorado , Boulder, CO 80309
                Author notes
                1To whom correspondence should be addressed. Email: mccollom@ 123456lasp.colorado.edu .

                Edited by John M. Hayes, Woods Hole Oceanographic Institution, Berkeley, CA, and approved September 13, 2016 (received for review July 18, 2016)

                Author contributions: T.M.M. designed research, performed research, analyzed data, and wrote the paper.

                Author information
                http://orcid.org/0000-0002-3596-5588
                Article
                PMC5150391 PMC5150391 5150391 201611843
                10.1073/pnas.1611843113
                5150391
                27821742
                fcbbed3e-7a7f-464e-9349-f9205e93b8bb
                History
                Page count
                Pages: 6
                Funding
                Funded by: NSF | Directorate for Geosciences (GEO) 100000085
                Award ID: OCE 0927744
                Categories
                Physical Sciences
                Earth, Atmospheric, and Planetary Sciences
                From the Cover

                hydrothermal systems,abiotic methane,serpentinization

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