Lead 210 and silicate profiles from sediments of the equatorial Pacific and South Atlantic

Particle mixing rates have been determined for 5 South Atlantic/Antarctic and 3 equatorial Pacific deep-sea cores using excess 210Pb and 32Si measurements. Radionuclide profiles from these siliceous, calcareous, and clay-rich sediments have been evaluated using a steady state vertical advection diffusion model. In Antarctic siliceous sediments210Pb mixing coefficients (0.04-0.16 cm**2/y) are in reasonable agreement with the 32Si mixing coefficient (0.2 or 0.4 cm**2/y, depending on 32Si half-life). In an equatorial Pacific sediment core, however, the 210Pb mixing coefficient (0.22 cm**2/y) is 3-7 times greater than the 32Si mixing coefficient (0.03 or 0.07 cm**2/y). The difference in 210Pb and 32Si mixing rates in the Pacific sediments results from: (1) non-steady state mixing and differences in characteristic time and depth scales of the two radionuclides, (2) preferential mixing of fine-grained clay particles containing most of the 210Pb activity relative to coarser particles (large radiolaria) containing the 32Si activity, or (3) the supply of 222Rn from the bottom of manganese nodules which increases the measured excess 210Pb activity (relative to 226Ra) at depth and artificially increases the 210Pb mixing coefficient. Based on 32Si data and pore water silica profiles, dissolution of biogenic silica in the sediment column appears to have a minor effect on the 32Si profile in the mixed layer. Deep-sea particle mixing rates reported in this study and the literature do not correlate with sediment type, sediment accumulation rate, or surface productivity. Based on differences in mixing rate among three Antarctic cores collected within 50 km of each other, local variability in the intensity of deep-sea mixing appears to be as important as regional differences in sediment properties.

ODP Site 162-980 age model and color reflectance record of sediments from ODP Leg 162 sites

Sediment spectral reflectance measurements were generated aboard the JOIDES Resolution during Ocean Drilling Program Leg 162 shipboard operations. The large size of the raw data set (over 1.3 gigabytes) and limited computer hard disk storage space precluded detailed analysis of the data at sea, although broad band averages were used as aids in developing splices and determining lithologic boundaries. This data report describes the methods used to collect these data and their shipboard and postcruise processing. These initial results provide the basis for further postcruise research.

Calcareous nannofossil range-distribution and zonation of sediments from three ODP Leg 205 holes

Ocean Drilling Program Leg 205 of the research vessel JOIDES Resolution was a return expedition to the Leg 170 sites located on the Costa Rica subduction zone. Here the entire sediment cover on the incoming Cocos plate, including significantly large sections of calcareous nannofossil ooze and chalk, is underthrust beneath the overriding Caribbean plate. The large amount of subducted carbonate produces characteristic styles of volcanic and seismic activity that differ from those found farther along strike in Nicaragua and elsewhere. An understanding of the fate of subducted carbonate sediment sections is an essential component to our understanding of the global biogeochemical cycling of carbon dioxide. Because Leg 205 drilling operations were performed within meters of the Leg 170 drill sites occupied during October-December 1996, minimal coring was done during Leg 205. Although the biostratigraphy of the Leg 170 sites has since been documented in detail, questions remained regarding the age and nature of a gabbro sill that was only partially penetrated by coring during Leg 170. Coring operations during Leg 205 fully penetrated the gabbro sill, followed by an additional 12 m of sediments below the sill, and then ~160 m of gabbro. Coring halted at 600 meters below seafloor (mbsf). Calcareous nannofossil age dating of the sediments immediately above the igneous sill, as well as the sediment between the sill and the lower igneous unit, indicates a minimum age of 15.6 Ma and a maximum age of 18.2 Ma for the sediments. This implies that the sill was emplaced more recently than 18.2 Ma. The calcareous nannofossil assemblage in baked sediments in contact with the top of the lower igneous unit also suggests that the maximum age for emplacement is 18.2 Ma. At Site 1254, coring was accomplished between 150 and 230 mbsf (prism section), and from 300 to 367.5 mbsf (prism and through the décollement into the underthrust section). In the interval from 150 to 322 mbsf, the biostratigraphic analysis of calcareous nannofossils suggests that the sediments are early Pleistocene age between 150 and 161 mbsf, late Pliocene age from 161 to 219 mbsf, and early Pliocene age from 219 to 222 mbsf (no younger than 3.75 Ma). The lack of marker fossils in the interval of sediments cored from 300 to 350.6 mbsf does not allow for any age determinations; however, sediments from 351.6 to 359.81 mbsf could be age dated and are also early Pliocene age, but no younger than 3.75 Ma.

Moleculare composition of sediments from ODP Hole 116-717C

We describe the molecular composition of a portion of the solvent-soluble organic material (lipid extract), from three organic rich muds (samples 116-717C-22X-1, 80-86 cm, 116-717C-34X-3, 130-135 cm, and 116-717C-55X-1, 65-70 cm). These samples were taken from Hole 717C, located on the Bengal Fan at a position of 0°55.8'S and 81°23.4'E. Both the palaeoenvironmental and digenetic significance of these lipid distributions have been assessed and found to be consistent with their suspected origins, i.e., turbidites from the upper slope of the western Bay of Bengal and the Ganges-Brahmaputra delta.

(Table T1) Calcium carbonate content of sediments from ODP Leg 172 sites

Visual-domain diffuse reflectance data collected aboard the JOIDES Resolution with the Minolta spectrometer CM-2002 during Ocean Drilling Program Leg 172 have been used to estimate successfully the carbonate content of sediments. Calibration equations were developed for each site and for each lithostratigraphic unit (or subunit at Site 1063) using multiple linear regression on raw as well as pretreated reflectance spectra (i.e., first-order derivation and squaring of raw reflectance spectra) for a total of 4141 direct carbonate measurements. The root-mean-square errors of 4% to 7% are within the range of previous estimates using diffuse reflectance data and are acceptable for the general extensive range of carbonate contents (i.e., 0-70 wt%) that characterize sedimentation at Leg 172 sites.

(Appendix) Chemical composition of bottom sediments at DSDP Leg 72 Holes

The distributions of calcium carbonate, of amorphous silica, and of 21 chemical compounds and elements in sediments of Holes 515A, 515B, 516, 516F, 517, and 518 are highly nonuniform; they change depending on the sediment types, grain size, and mineral composition. The main source of the lithogenous elements (K, Li, Rb, Fe, Ti, Zr, Ni, Cr, Sn) is terrigenous matter of South America. These elements correlate well or at least satisfactorily with each other and with the sum of clay minerals. CaCO3, amorphous SiO2 and organic C form a second group, the main source of which is biota of the ocean. Zn, Cu, Ba, Mo, (V, Na) are a third group, which is supplied by both terrigenous and biogenic matter. Judging by the distribution of chemical elements and components in sediments of Site 515, this area of the Brazil Basin is characterized by the rather constant conditions of pelagic terrigenous sedimentation from upper Eocene till Holocene. Small changes in chemical composition of sediments throughout the section are linked mainly to the evolution of subaerial source provinces, changes in hydrodynamic regime, and fluctuations of the ocean level. The chemical composition of sediments from the Rio Grande Rise sites suggests the existence of three main stages of sedimentation in this area. The first stage is the initial period of sediment accumulation on basalts at the beginning of the Late Cretaceous. Then followed sedimentary conditions notable for their sharp changes in chemical composition and type. Beginning in the middle Eocene and persisting into the Holocene, stable conditions of sedimentation characterize a third stage, represented by the formation of approximately 700 m of nannofossil oozes of rather monotonous chemical composition.