Interstitial water chemsitry at DSDP Leg 60 Holes

Interstitial water data obtained during Leg 60 show complex gradients at Site 453 in a sediment pond on the west side of the Mariana Trough. Concentrations of Ca, Mg, Sr, as well as of K and Li, suggest that slightly altered sea water penetrates below the sediments, most likely through brecciated igneous and metamorphic rocks, mainly gabbros, lying at the base of the pond. Interstitial water concentration gradients suggest that reactions involving igneous matter lead to increases in calcium and strontium in the pore fluids and to decreases in magnesium. Upward advection of water through the sediments does not appear to occur, so that the advected sea water most likely penetrates deeper into the breccias, perhaps leading to further hydrothermal activity elsewhere in this area. Interstitial water gradients at Sites 458 (conservative) and 459 suggest that reactions in the sediments and underlying basalts are responsible for increases in dissolved calcium and decreases in magnesium and potassium.

(Table 1) Sample description and tetrapyrrole pigment yield at DSDP Leg 60 Holes

In order to provide a better understanding of the fate of sedimentary chlorophyll and chlorophyll degradation products in all kinds of environments, we have recently expanded our studies to include examination of sediments returned from Legs which are not rich in organic matter, nor are even primarily biogenic. Eight core samples from the Mariana Basin and Trench, obtained from DSDP Leg 60, were analyzed for products of chlorophyll diagenesis. To date, the sediment samples from the South Philippine Sea have been the most organically barren examined. Through elimination of the bias of examining only sediments rich in organic matter, we hope that the fate of chlorophyllous material on a more global scale will eventually be elucidated.

Calcium carbonate global LGM Burial rate data

Global databases of calcium carbonate concentrations and mass accumulation rates in Holocene and last glacial maximum sediments were used to estimate the deep-sea sedimentary calcium carbonate burial rate during these two time intervals. Sparse calcite mass accumulation rate data were extrapolated across regions of varying calcium carbonate concentration using a gridded map of calcium carbonate concentrations and the assumption that accumulation of noncarbonate material is uncorrelated with calcite concentration within some geographical region. Mean noncarbonate accumulation rates were estimated within each of nine regions, determined by the distribution and nature of the accumulation rate data. For core-top sediments the regions of reasonable data coverage encompass 67% of the high-calcite (>75%) sediments globally, and within these regions we estimate an accumulation rate of 55.9 ± 3.6 x 10**11 mol/yr. The same regions cover 48% of glacial high-CaCO3 sediments (the smaller fraction is due to a shift of calcite deposition to the poorly sampled South Pacific) and total 44.1 ± 6.0 x 10**11 mol/yr. Projecting both estimates to 100 % coverage yields accumulation estimates of 8.3 x 10**12 mol/yr today and 9.2 x 10**12 mol/yr during glacial time. This is little better than a guess given the incomplete data coverage, but it suggests that glacial deep sea calcite burial rate was probably not considerably faster than today in spite of a presumed decrease in shallow water burial during glacial time.

Description and chemical composition of ferromanganese encrustations and deposits in the Atlantic Ocean from R/V Atlantis II cruises 20, 42, 60, 85; R/V Chain cruise 35; R/V Knorr cruise 61 and RRS Shackleton cruise 75/1 stations

Chemical and mineralogical compositions of ferromanganese oxide coatings on rocks dredged from the New England Seamounts, the Sierra Leone Rise and the Mid-Atlantic Ridge near the Equator have been determined in an investigation of regional differences in Atlantic ferromanganese deposits. Most encrustations are clearly of hydrogenous origin, consisting mainly of todorokite and delta MnO2, but several recovered from the equatorial fracture zones may be hydrothermal accumulations. Differences in the chemistry of the water column and in growth rates of the ferromanganese coatings may be important in producing this regional contrast in composition. Fine-scale changes in element abundances within the encrustations indicate that the nature of the substrate has little influence on compositional variations.