Oxygen isotopic composition of interstitial waters from ODP Leg 207 sites

We determined oxygen isotopic compositions of interstitial water (IW) recovered during Ocean Drilling Program Leg 207. Five sites were cored (3200- to 1900-m water depth) on Demerara Rise off Suriname, South America, recovering a Cenomanian-Paleogene sedimentary sequence consisting of black shales and chalks. A total of 115 IW oxygen isotopic analyses are presented.

Isotopic composition of carbon in organic matter of sediments and particulate matter from the Northwest Pacific

A study was made of isotopic composition of carbon in lipids found in three samples of separate particulates and in eight bottom sediment samples collected in a from the Simushir Island towards the open Pacific Ocean. Average d13C of lipids from particulates was 2.3 per mil lower than one of sediments. Humic acids from sediments are the most isotopically heavy fraction (d13C = -21.2 per mil). Isotopic composition of carbon in lipids depended on their total content in samples and on composition of sediments. Formation of isotopically heavy lipids in the surface layer of sediments may be associated with biogeochemical resynthesis of humic acids.

Sulphate concentrations and sulphur isotopic composition in pore fluids from ODP Leg 168 sites

A numerical model of sulfate reduction and isotopic fractionation has been applied to pore fluid SO4**2- and d34S data from four sites drilled during Ocean Drilling Program (ODP) Leg 168 in the Cascadia Basin at 48°N, where basement temperatures reach up to 62°C. There is a source of sulfate both at the top and the bottom of the sediment column due to the presence of basement fluid flow, which promotes bacterial sulfate reduction below the sulfate minimum zone at elevated temperatures. Pore fluid d34S data show the highest values (135 per mil) yet found in the marine environment. The bacterial sulfur isotopic fractionation factor, a, is severely underestimated if the pore fluids of anoxic marine sediments are assumed to be closed systems and Rayleigh fractionation plots yield erroneous values for a by as much as 15 per mil in diffusive and advective pore fluid regimes. Model results are consistent with a = 1.077+/-0.007 with no temperature effect over the range 1.8 to 62°C and no effect of sulfate reduction rate over the range 2 to 10 pmol/ccm/day. The reason for this large isotopic fractionation is unknown, but one difference with previous studies is the very low sulfate reduction rates recorded, about two orders of magnitude lower than literature values that are in the range of µmol/ccm/day to tens of nmol/ccm/day. In general, the greatest 34S depletions are associated with the lowest sulfate reduction rates and vice versa, and it is possible that such extreme fractionation is a characteristic of open systems with low sulfate reduction rates.