(Table 1) Color, Fe-C-S chemistry and carbonate content from ODP Sites 172-1062 and 172-1063

Reflectance spectra collected during ODP Leg 172 were used in concert with solid phase iron chemistry, carbonate content, and organic carbon content measurements to evaluate the agents responsible for setting the color in sediments. Factor analysis has proved a valuable and rapid technique to detect the local and regional primary factors that influence sediment color. On the western North Atlantic drifts, sediment color is the result of primary mineralogy as well as diagenetic changes. Sediment lightness is controlled by the carbonate content while the hue is primarily due to the presence of hematite and Fe2+/Fe3+ changes in clay minerals. Hematite, most likely derived from the Permo-Carboniferous red beds of the Canadian Maritimes, is differentially preserved at various sites due to differences in reductive diagenesis and dilution by other sedimentary components. Various intensities for diagenesis result from changes in organic carbon content, sedimentation rates, and H2S production via anaerobic methane oxidation. Iron monosulfides occur extensively at all high sedimentation sites especially in glacial periods suggesting increased high terrigenous flux and/or increased reactive iron flux in glacials.

Chemistry of igneous rocks of DSDP Leg 30 holes

Igneous rock units were encountered at four of the five sites drilled on Leg 30 of the Deep Sea Drilling Project. These units uncluded a diabase sill at Site 285, a basalt underlain by a gabbro at 286, two basalt flows at 287, and a basalt flow at 289. Site 285 is located approximately in the center of the South Fiji Basin, Site 286 is adjacent to a filled portion of the New Hebrides Trench, Site 287 is adjacent to a basement high in the Coral Sea Basin, and Sites 288 and 289 are located on the Ontong-Java Plateau north of the Solomon Islands (Figure 1). Figure 2 presents generalized lithologic columns for the igneous rock units found at these sites. When a unit number is given, e.g., Site 286, Unit 4 basalt, this number conforms with the unit number assigned to it in the overall stratigraphic sequence of that hole as defined in the individual Site Reports in this volume. Unless otherwise stated, depths are given as measured from the sediment-igneous rock contact rather than the mudline.

Seawater carbonate chemistry, primary production, biomass and calcification of plankton and bacteria, 2009

Production (abundance and biomass) and net calcification rates of the coccolithophorid Pleurochrysis carterae under different partial pressures of CO2 (pCO2) were examined using short (15, 24 and 39 h), long (7 d) and dark (7 d) incubation experiments. Short incubations were conducted at ambient, 500 and 820 ppm pCO2 levels in natural seawater that was enriched with nutrients and inoculated with P. carterae. Long incubations were conducted at ambient and 1200 ppm pCO2 levels in natural seawater (0.2 µm filtered as well as unfiltered) that was enriched with nutrients and inoculated with P. carterae. Dark incubations were conducted at ambient and 1200 ppm pCO2 in unfiltered seawater that was inoculated with P. carterae. The abundance and biomass of coccolithophorids increased with pCO2 and time. The abundance and biomass of most noncalcifying phytoplankton also increased, and were hardly affected by CO2 inputs. Net calcification rates were negative in short incubations during the pre-bloom phase regardless of pCO2 levels, indicating dissolution of calcium carbonate. Further, the negative values of net calcification in short incubations became less negative with time. Net calcification rates were positive in long incubations during blooms regardless of pCO2 level, and the rate of calcification increased with pCO2. Our results show that P. carterae may adapt to increased (~1200 ppm) pCO2 level with time, and such increase has little effect on the ecology of noncalcifying groups and hence in ecosystem dynamics. In dark incubations, net calcification rates were negative, with the magnitude being dependent on pCO2 levels.

Rubidium and Strontium chemistry of oceanic crust

Times of vein mineral deposition in the ocean crust have been determined both by Rb-Sr isochron ages of vein smectites and by comparison of 87Sr/86Sr ratios of vein calcites with the known variations of seawater 87Sr/86Sr ratio with time. Results from drilling sites 105, 332B and 418A, Atlantic Ocean, which have basement formation ages of 155 m.y., 3.5 m.y., and 110 m.y., respectively, show that vein deposition is essenrially complete within 5-10 m.y. after formation of the basaltic crust. This provids direct evidence that hydrothermal circulation of sea-water through the oceanic crust is an important process for only 5-10 m.y. after crust formation.

Seawater carbonate chemistry and calcification rate in flume experiment

Ocean acidification (OA) poses a severe threat to tropical coral reefs, yet much of what is know about these effects comes from individual corals and algae incubated in isolation under high pCO2. Studies of similar effects on coral reef communities are scarce. To investigate the response of coral reef communities to OA, we used large outdoor flumes in which communities composed of calcified algae, corals, and sediment were combined to match the percentage cover of benthic communities in the shallow back reef of Moorea, French Polynesia. Reef communities in the flumes were exposed to ambient (400 ?atm) and high pCO2 (1300 ?atm) for 8 weeks, and calcification rates measured for the constructed communities including the sediments. Community calcification was reduced by 59% under high pCO2, with sediment dissolution explaining ~ 50% of this decrease; net calcification of corals and calcified algae remained positive but was reduced by 29% under elevated pCO2. These results show that, despite the capacity of coral reef calcifiers to maintain positive net accretion of calcium carbonate under OA conditions, reef communities might transition to net dissolution as pCO2 increases, particularly at night, due to enhanced sediment dissolution.