Concentrations and isotopic compositions of ethane and propane in cold, deeply buried sediments from the southeastern Pacific are best explained by microbial production of these gases in situ. Reduction of acetate to ethane provides one feasible mechanism. Propane is enriched in 13 C relative to ethane. The amount is consistent with derivation of the third C from inorganic carbon dissolved in sedimentary pore waters. At typical sedimentary conditions, the reactions yield free energy sufficient for growth. Relationships with competing processes are governed mainly by the abundance of H2. Production of C2 and C3 hydrocarbons in this way provides a sink for acetate and hydrogen but upsets the general belief that hydrocarbons larger than methane derive only from thermal degradation of fossil organic material.ethanogenesis ͉ hydrocarbon gases ͉ marine sediments ͉ propanogenesis ͉ stable carbon isotopes L eg 201 of the Ocean Drilling Program was dedicated to the study of microbial life in deeply buried marine sediments (1, 2). Cores were obtained from open-ocean sites in the Equatorial Pacific, where sediments deposited 40 million years ago are underlain by seafloor basalts through which oxygenated seawater is flowing, and from the Peruvian Margin, where drilling penetrated sediments up to 15 million years old (Fig. 1). Temperatures in sediments ranged from 2°C to 25°C. All sites are isolated from reservoirs of fossil hydrocarbons. At both openocean and ocean-margin sites, treatment of sediments with strong base released ethane and propane (Fig. 2). When the treatment was repeated with fresh sediment and isotopically labeled water (␦D ϭ ϩ4000‰), no excess deuterium appeared in the ethane or propane. Therefore, we conclude that the hydrocarbons were strongly sorbed, indigenous constituents of the sediment and did not derive from a chemical reaction between the strong base and an organic substrate.Earlier reports describe sediments offshore Peru (3) and Spitsbergen (4), from which similar mixtures of hydrocarbons could be released by treatment with hot solutions of phosphoric acid. In each case, the carbon-isotopic compositions and abundance ratios (C 1 ͞C 2ϩ ) led to reluctant suggestions that the gases must be of thermogenic origin and thus have migrated into the unconsolidated seafloor sediments: ''the [postulated] migration of C 2ϩ hydrocarbons. . . is somehow related to these fluids [brines that might have flowed from one basin to another]'' (3); and ''. . . elevated seepages [of thermogenic hydrocarbons] occurred irregularly but are not currently active. . . it remains speculative whether the detected hydrocarbon anomalies are related to reservoirs and͞or active source rocks'' (4). No mechanism for sorbing the putatively migrated hydrocarbons more strongly than indigenous microbial products has been offered.Ethane and propane with similar isotopic characteristics and abundance ratios have recently been reported in Cretaceous marine shales in the Western Canadian sedimentary basin (5). Previous work has also pointe...