Concentration and isotope composition of sulphur in sediments and pore water at DSDP Leg 70 Holes

Data obtained while investigating the mounds area near the Galapagos Spreading Center demonstrate the direct influence of solutions derived from the interaction of seawater and young oceanic crust on the sedimentary cover. Investigation of metalliferous sediments from the mid-oceanic ridges, the Galapagos mounds, and the FAMOUS-area zone formations have shown that this influence and the resulting products are dependent on composition, temperature, and conditions of solution input. The study of sulfur in upwardly migrating solutions and the interaction of these solutions with sediments is of great interest. Investigations of different types of hydrothermally derived formations (Edmond, et al., 1979; Spiess et al., 1980; Styrt et al., 1981; Rosanova 1976; Grinenko et al., 1978) have shown the significant role of sulfur-bearing minerals in deposits formed from hightemperature solutions. In contrast, the addition of hydrothermal sulfur is negligible in those metalliferous sediments that precipitated as a result of the interaction between the solutions and open seawater (Bonatti et al., 1972, 1976; Gordeev et al., 1979; Migdisov, Bogdanov, et al., 1979). For example, sulfides are absent in clearly oxidized metalliferous sediments from the East Pacific Rise (EPR). Barite sulfur from these sediments is identical with seawater sulfate sulfur in isotope composition (Grinenko et al., 1978). Gurvich and Bogdanov (1977) have suggested that barium from EPR metalliferous sediments results completely from biological activity and from the components of ocean waters. Edmond et al. (1979) report that low-temperature springs from the Galapagos Rift axis contain two types of solutions: those with and those without H2S.

Rb-Sr isotope systematics and Sr/Ca-Ba/Ca ratios at DSDP Hole 89-462A

Four samples of Nauru Basin basalts (Cores 94 to 109 of Hole 462A, sub-bottom depth 1077-1209 m) have 87Sr/86Sr ratios in the range 0.7037 to 0.7038, which is distinctly higher than the ratios of N-type MORB. The Rb contents of the samples are depleted in comparison with those of MORB and ocean-island basalts. These chemical and isotopic characteristics are identical to those of the basalts previously drilled during Leg 61 (Cores 75 to 90 of Hole 462A), and are explained in terms of inhomogeneity of the source region in the mantle or later alteration effects. Sr/Ca-Ba/Ca systematics of 15 samples from Cores 462A-94 to 462A-109 and 14 samples from Cores 462A-75 to 462A-90 suggest that the Nauru Basin basalts are derived from a mantle peridotite by 20 to 30% partial melting with subsequent Plagioclase crystallization.

Chiasmolithus species in middle Eocene and Oligocene sediments of ODP Holes 105-647A and 120-748B

In this preliminary biometric study of the calcareous nannofossil species Chiasmolithus expansus, Chiasmolithus oamaruensis, and Chiasmolithus altus from the upper middle Eocene to lower Oligocene of Sites 647 and 748, we document a complete gradation of forms among all three species. Chiasmolithus oamaruensis has significantly higher morphologic variance than the other species. The Chiasmolithus population at each site changes from C. expansus to C. oamaruensis and then to C. altus. This may not reflect a true evolutionary sequence because a major reversal in shape change of the central cross-bar structure accompanies this sequence, and because C. altus is morphologically closer to C. expansus than it is to C. oamaruensis. The change in the width of the cross-bar structure is primarily a result of changes in the alignment of the central connecting bar, rather than of changes in the cross-bar angle. At Site 748, two fluctuations in morphology produce sample populations intermediate between all three species. In addition, reported stratigraphic and paleogeographic occurrences of C. oamaruensis and C. altus show different latitudinal distributions. These morphological and distributional patterns may be explained by a continuous morphologic gradient between C. oamaruensis and C. altus, with C. oamaruensis occurring more commonly in cool-water paleoenvironments, and C. altus occurring more commonly in cold-water paleoenvironments. Thus, paleoenvironmental fluctuations at Site 748 may be the cause of the morphologic fluctuations in Chiasmolithus. This hypothesis can be tested against previously proposed evolutionary models by more detailed sampling of sections along a latitudinal transect.