Please cite this article as: Stolper, D.A., Martini, A.M., Clog, M., Douglas, P.M., Shusta, S.S., Valentine, D.L., Sessions, A.L., Eiler, J.M., Distinguishing and understanding thermogenic and biogenic sources of methane using multiply substituted isotopologues, Geochimica et Cosmochimica Acta (2015), doi: http://dx. Abstract: Sources of methane to sedimentary environments are commonly identified and quantified using the stable-isotopic compositions of methane. The methane "clumped-isotope geothermometer", based on the measurement of multiply substituted methane isotopologues (13 CH 3 D and 12 CH 2 D 2), shows promise in adding new constraints to the sources and formational environments of both biogenic and thermogenic methane. However, questions remain about how this geothermometer behaves in systems with mixtures of biogenic and thermogenic gases and different biogenic environments. We have applied the methane clumped-isotope thermometer to a mixed biogenic-thermogenic system (Antrim Shale, USA) and to biogenic gas from gas seeps (Santa Barbara and Santa Monica Basin, USA), a pond on the Caltech campus, and methanogens grown in pure-culture. We demonstrate that clumped-isotope based temperatures add new quantitative constraints to the relative amounts of biogenic vs. thermogenic gases in the Antrim Shale indicating a larger proportion (~50%) of thermogenic gas in the system than previously thought. Additionally, we find that the clumped-isotope temperature of biogenic methane appears related to the environmental settings in which the gas forms. In systems where methane generation rates appear to be slow (e.g., the Antrim Shale and gas seeps), microbial methane forms in or near both internal isotopic equilibrium and hydrogen-isotope equilibrium with environmental waters. In systems where methane forms rapidly, microbial methane is neither in internal isotopic equilibrium nor hydrogen-isotope equilibrium with environmental waters. A quantitative model of microbial methanogenesis that incorporates isotopes is proposed to explain these results.

Paleoclimate studies suggest that increased global warmth during the Eocene epoch was greatly amplified at high latitudes, a state that climate models cannot fully reproduce. However, proxy estimates of Eocene near-Antarctic sea surface temperatures (SSTs) have produced widely divergent results at similar latitudes, with SSTs above 20°C in the southwest Pacific contrasting with SSTs between 5 and 15°C in the South Atlantic. Validation of this zonal temperature difference has been impeded by uncertainties inherent to the individual paleotemperature proxies applied at these sites. Here, we present multiproxy data from Seymour Island, near the Antarctic Peninsula, that provides well-constrained evidence for annual SSTs of 10-17°C (1σ SD) during the middle and late Eocene. Comparison of the same paleotemperature proxy at Seymour Island and at the East Tasman Plateau indicate the presence of a large and consistent middle-to-late Eocene SST gradient of ∼7°C between these two sites located at similar paleolatitudes. Intermediate-complexity climate model simulations suggest that enhanced oceanic heat transport in the South Pacific, driven by deep-water formation in the Ross Sea, was largely responsible for the observed SST gradient. These results indicate that very warm SSTs, in excess of 18°C, did not extend uniformly across the Eocene southern high latitudes, and suggest that thermohaline circulation may partially control the distribution of high-latitude ocean temperatures in greenhouse climates. The pronounced zonal SST heterogeneity evident in the Eocene cautions against inferring past meridional temperature gradients using spatially limited data within given latitudinal bands.paleooceanography | clumped isotopes | organic geochemistry | climate modeling | high-latitude climate

Highlights:-We present a review and an expanded dataset of methane clumped isotope measurements.-Methane clumped isotope values often indicate equilibrium formation temperature.-Kinetic effects during or after methane production can affect clumped isotope values.-The wide variability in clumped isotope values suggests it will be a useful tracer. AbstractThe isotopic composition of methane is of longstanding geochemical interest, with important implications for understanding petroleum systems, atmospheric 3 greenhouse gas concentrations, the global carbon cycle, and life in extreme environments.Recent analytical developments focusing on multiply substituted isotopologues ('clumped isotopes') are opening a valuable new window into methane geochemistry.When methane forms in internal isotopic equilibrium, clumped isotopes can provide a direct record of formation temperature, making this property particularly valuable for identifying different methane origins. However, it has also become clear that in certain settings methane clumped isotope measurements record kinetic rather than equilibrium isotope effects. Here we present a substantially expanded dataset of methane clumped isotope analyses, and provide a synthesis of the current interpretive framework for this parameter. In general, clumped isotope measurements indicate plausible formation temperatures for abiotic, thermogenic, and microbial methane in many geological environments, which is encouraging for the further development of this measurement as a geothermometer, and as a tracer for the source of natural gas reservoirs and emissions.We also highlight, however, instances where clumped isotope derived temperatures are higher than expected, and discuss possible factors that could distort equilibrium formation temperature signals. In microbial methane from freshwater ecosystems, in particular, clumped isotope values appear to be controlled by kinetic effects, and may ultimately be useful to study methanogen metabolism.

This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. temperature. In some microbial methane, however, non-equilibrium isotope effects, 34 probably related to the kinetics of methanogenesis, lead to low clumped isotope values. 35We identify four categories of emissions in the studied samples: thermogenic methane, 36 deep subsurface or marine microbial methane formed in isotopic equilibrium, freshwater 37 microbial methane with non-equilibrium clumped isotope values, and mixtures of 38 microbial and thermogenic methane (i.e., combinations of the first three end members). 39Mixing between thermogenic and microbial methane produces a non-linear variation in 40clumped isotope values with mixing proportion that provides new constraints for the 41 formation environment of the mixing end-members. Analyses of microbial methane 42 emitted from lakes, as well as a methanol-consuming methanogen pure culture, support 43 the hypothesis that non-equilibrium clumped isotope values are controlled, in part, by 44 kinetic isotope effects induced during enzymatic reactions involved in methanogenesis. 45Our results indicate that these kinetic isotope effects vary widely in microbial methane 46 3 produced in Arctic lake sediments, with non-equilibrium ∆ 18 values spanning a range of 47 more than 5‰. 48 49