Concentrations and δ 34 S and δ 13 C values were determined on SC^", HCO 3 ", CO 2 , and CH 4 in interstitial water and gas samples from the uppermost 400 m of sediment on the Blake Outer Ridge. These measurements provide the basis for detailed interpretation of diagenetic processes associated with anaerobic respiration of electrons generated by organic-matter decomposition. The sediments are anaerobic at very shallow depths (< 1 m) below the seafloor. Sulfate reduction is confined to the uppermost 15 m of sediment and results in a significant outflux of oxidized carbon from the sediments. At the base of the sulfate reduction zone, upward-diffusing CH 4 is being oxidized, apparently in conjunction with SC^~ reduction. CH 4 generation by CO 2 reduction is the most important metabolic process below the 15-m depth. CO 2 removal is more rapid than CO 2 input over the depth interval from 15 to 100 m, and results in a slight decrease in HCO 3~ concentration accompanied by a 40‰ positive shift in δ 13 C. The differences among coexisting CH 4 , CO 2 , and HCOf are consistent with kinetic fractionation between CH 4 and dissolved CO 2 , and equilibrium fractionation between CO 2 and HCO 3 ". At depths greater than 100 m, the rate of input of CO 2 (δ 13 C = -25‰) exceeds by 2 times the rate of removal of CO 2 by conversion to CH 4 (δ 13 C of -60 to -65‰). This results in an increase of dissolved HCO 3 " concentration while maintaining δ 13 C of HCO 3 " relatively constant at -I-lO‰. Non-steady-state deposition has resulted in significantly higher organic carbon contents and unusually high (70 meq I" 1 ) pore-water alkalinities below 150 m. These high alkalinities are believed to be related more to spontaneous decarboxylation reactions than to biological processes. The general decrease in HCOf concentration with constant δ 13 C over the depth interval of 200 to 400 m probably reflects increased precipitation of authigenic carbonate.Input-output carbon isotope-mass balance calculations, and carbonate system equilibria in conjunction with observed CO 2 -CH 4 ratios in the gas phase, independently suggest that CH 4 concentrations on the order of 100 mmol kg" 1 are present in the pore waters of Blake Outer Ridge sediments. This quantity of CH 4 is believed to be insufficient to saturate pore waters and stabilize the CH 4 6H 2 O gas hydrate. Results of these calculations are in conflict with the physical recovery of gas hydrate from 238 m, and with the indirect evidence (seismic reflectors, sediment frothing, slightly decreasing salinity and chlorinity with depth, and pressure core barrel observations) of gas-hydrate occurrence in these sediments. Resolution of this apparent conflict would be possible if CH 4 generation were restricted to relatively thin (1-10 m) depth intervals, and did not occur uniformly at all depths throughout the sediment column, or if another methanogenic process (e.g., acetate fermentation) were a major contributor of gas.