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T.M. Vogel

Publications and source records attributed to T.M. Vogel.

2 recordsLinked to original sources

Low-temperature formation of hydrocarbon gases in San Francisco Bay sediment (California, U.S.A.)

To understand the processes responsible for the presence of low-molecular-weight hydrocarbons (C1-C4) in anoxic environments, we studied sediments collected from an anaerobic estuarine mudflat. In these sediments methane (C1) was several orders of magnitude more abundant than all other C2-C4 hydrocarbons; the C1 (C2 + C3) ratio was ??? 13,000. Mean ethane/ethene and propane/propene ratios were 0.4 and 0.7, respectively. Production of C1-C4 hydrocarbons was monitored during prolonged incubation (7 months) of sediments at 27?? and 4??C. Samples stored at 27??C generated significant quantities of C1-C4 hydrocarbon gases. Incubation at 4??C inhibited production of these gases. Several bactericides were tested with respect to their ability to inhibit formation of gaseous hydrocarbons. Sodium azide, chloroform, and 2-bromoethanesulfonic acid effectively inhibited methane formation, but not ethene formation in dilute continuously-shaken sediment slurries. Zephiran chloride only caused partial inhibition of methanogenesis (46%) and ethene generation (34%) in these slurries. In experiments with more concentrated unshaken sediment slurries, however, zephiran chloride and sodium azide did not block formation of methane, ethane, or propane. Only storage at -10??C prevented production of these gases. These results indicate that C1-C4 hydrocarbons can be formed by low-temperature reactions, possibly mediated by microorganisms. ?? 1982.

Chemical Geology

Geochemical prospecting for hydrocarbons in the outer continental shelf, Southern Bering Sea, Alaska

This geochemical survey is based on 20 stations located on the outer continental shelf of the southern Bering Sea in an area of 30,000 km 2 that includes St. George basin. Hydrocarbon gases from sediment samples recovered by gravity coring at each of the stations were analyzed by gas chromatography. Data are summarized for a subbottom depth of 0.5 m, because core penetration, although variable, reached at least this depth at all of these stations. Two parameters were used to distinguish the possible presence of thermogenic hydrocarbons: (1) ratios less than 50 of methane to ethane plus propane; and (2) ratios greater than 1 of ethane to ethene. No major hydrocarbon anomalies were discovered; however, at two stations at the northern end of St. George basin, our data indicate that thermogenic hydrocarbons may be present at depth. Major faulting in the vicinity of these stations could provide the pathways for the gas.

Journal of Geochemical Exploration