928 resultados para Start Sites


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The ocean history of reactive phosphorus (P) (i.e., dissolved P available to fuel oceanic primary productivity) is of interest because of the role of P as a biolimiting nutrient, and knowledge of P burial in marine sediments is key to testing hypotheses about temporal changes in P input or output fluxes. Our understanding of the history of the P cycle over the Cenozoic has increased substantially with temporal records of reactive P mass accumulation rates from open-ocean Pacific and Atlantic equatorial sites. However, questions about the relative importance of nutrient burial in ocean-margin sediments relative to burial in open-ocean sediments and about the extent of P remobilization in organic-rich, reducing environments characteristic of margin sediments remain unresolved. Nutrient burial in oceanic boundary current systems has been suggested to have a controlling role in oceanic nutrient budgets in certain time intervals (Vincent and Berger, 1985, doi:10.1029/GM032p0455), with higher sediment accumulation rates balancing the limited spatial extent of these sediments. Some investigators suggest that remobilization of P from reducing sediments in margin settings is a significant positive feedback to primary productivity (e.g., Van Cappellan and Ingall, 1994, doi:10.1029/94PA01455), whereas other results indicate that both P uptake and P release may occur in these settings depending on the balance of organic carbon and iron supply to the sediments and on the oxygenation of bottom waters (McManus et al., 1997, doi:10.1016/S0016-7037(97)00138-5). It is important to quantitatively understand the geochemistry of reactive P in margin sediments, where productivity and delivery of organic-rich material to the sediments in relatively shallow-water settings is often sufficient to promote anoxia in interstitial waters. To address these questions, we determined the P concentrations and geochemistry in sediment samples from eight sites drilled during Ocean Drilling Program (ODP) Leg 167, California margin (Sites 1010-1012, 1014, 1016-1017, and 1021-1022). These results are the first records of reactive P concentrations on long time scales-required for the calculation of P accumulation rates-for sediments from a highly productive eastern boundary current setting. In addition, we determined calcium carbonate contents and biogenic silica concentrations to define the environments of sedimentary production, burial, and diagenesis.

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During Leg 178, multiple advanced piston corer holes were drilled at four sites (1095, 1096, 1098, and 1099). Cores from the holes were correlated on board to produce composite depths and optimal spliced sections, but the time limitations aboard ship caused these to be preliminary. Recomputed composite depths for Sites 1098 and 1099 in Palmer Deep are reported elsewhere in this volume (doi:10.2973/odp.proc.sr.178.2002). This paper reports recomputed composite depths and spliced sections for Sites 1095 and 1096, located on a sediment drift on the continental rise of the Pacific margin of the Antarctic Peninsula. Limits on the validity of the spliced sections arise from limited multiple coverage and possibly from the effects of ocean swell.

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Six Deep Sea Drilling Project (DSDP) Sites (252, 285, 315, 317, 336, 386) were examined for the chemical composition of the dissolved salts in interstitial waters, the oxygen isotopic composition of the interstitial waters, and the major ion composition of the bulk solid sediments. An examination of the concentration-depth profiles of dissolved calcium, magnesium, potassium, and H218O in conjunction with oxygen isotope mass balance calculations confirms the hypothesis that in DSDP pelagic drill sites concentration gradients in Ca. Mg. K, and H218O are largely due to alteration reactions occurring in the basalts of Layer 2 and to alteration reactions involving volcanic matter dispersed in the sediment column. Oxygen isotope mass balance calculations require substantial alteration of Layer 2 (up to 25% of the upper 1000 m). but only minor exchange of Ca, Mg, and K occurs with the overlying ocean. This implies that alteration reactions in Layer 2 are almost isochemical.

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Diatoms occur sporadically in lower Miocene to Holocene sediments recovered at ODP Site 645 and in upper Pliocene to Holocene sediments at ODP Site 646. The diatom assemblage at Site 645 contains rare stratigraphic indicators. Fragmentation of frustules and the occurrence of species characteristic of high-latitude shelf, upper-slope environments suggest current transportation from the shelf. The diatom abundance and preservation at Site 646 probably reflect climatic changes and are also affected by dissolution, but it is not possible to detect the dominant factor. Therefore, the stratigraphic ranges of the primary and secondary biostratigraphic indicators are often unreliable.

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With this study, we investigate the mineralogical variations associated with the low-temperature (<100°C) alteration of normal tholeiitic pillow basalts varying in age from 0.8 to 3.5 Ma. Their alteration intensity varies systematically and is related to several factors, including (1) the aging of the igneous crust, (2) the increase of temperatures from the younger to the older sites, measured at the sediment/basement interface, (3) the local and regional variations in lithology and primary porosity, and (4) the degree of pillow fracturing. Fractures represent the most important pathways that allow significant penetration of fluids into the rock and are virtually the only factor controlling the alteration of the glassy rim and the early stages of pillow alteration. Three different alteration stages have been recognized: alteration of glassy margin, oxidizing alteration through fluid circulation in fracture systems, and reducing alteration through diffusion. All the observed mineralogical and chemical variations occurring during the early stages of alteration are interpreted as the result of the rock interaction with "normal," alkaline, and oxidizing seawater, along preferential pathways represented by the concentric and radial crack systems. The chemical composition of the fluid progressively evolves while moving into the basalt, leading to a reducing alteration stage, which is initially responsible for the precipitation of Fe-rich saponite and minor sulfides and subsequently for the widespread formation of carbonates. At the same time, the system evolved from being "water dominated" to being "rock dominated." No alteration effects in pillow basalts were observed that must have occurred at temperatures higher than those measured during Leg 168 at the basement/sediment interface (e.g., between 15° and 64°C).

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Sediment cores recovered from three holes drilled during Ocean Drilling Program Leg 136 include volcaniclastics probably derived from the Hawaiian islands. The volcaniclastics shallower than 10 meters below seafloor are fresh and are composed of basaltic glass (sideromelane), basaltic fragments (mainly tachylite), plagioclase, olivine, pyroxene, and opaque minerals. Most of these glasses are probably products of hydrovolcanism. Visibly, some of these volcaniclastics are recognized as bedded ash layers having thicknesses that range from 5 to 10 cm. However, many volcaniclastics are disrupted by bioturbation to some degree, and are sometimes totally mixed with ambient brown clays. No visible correlative ash layer among these holes was found. It seems that many ash layers thinner than the bedded layers were disrupted by bioturbation because of the low sedimentation rate of volcaniclastics. The volcaniclastics were probably transported one of two ways: through air fall and pelagic settling or through turbidity-current transport. Other archipelagic apron volcaniclastic sediments of volcanic seamounts suggest that turbidite transport is the favored explanation of origin.

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Benthic foraminiferal assemblages from northeast Atlantic DSDP Sites 609, 610, and 611 have been interpreted with reference to modern assemblages known to be linked with the overlying bottom-water masses. It is shown that the water masses in the late Miocene to Pleistocene were similar to those of today. The distribution of the water masses changed with time, however. Antarctic Bottom Water ("AABW"), which at present is restricted to the area south of the Azores, reached as far north as the Gibbs Fracture Zone in the early Pliocene. Increased production of North Atlantic Deep Water in the late Pliocene displaced the AABW to the south

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All holes drilled during Leg 114 contained ice-rafted debris. Analysis of samples from Hole 699A, Site 701, and Hole 704A yielded a nearly complete history of ice-rafting episodes. The first influx of ice-rafted debris at Site 699, on the northeastern slope of the Northeast Georgia Rise, occurred at a depth of 69.94 m below seafloor (mbsf) in sediments of early Miocene age (23.54 Ma). This material is of the same type as later ice-rafted debris, but represents only a small percentage of the coarse fraction. Significant ice-rafting episodes occurred during Chron 5. Minor amounts of ice-rafted debris first reached Site 701, on the western flank of the Mid-Atlantic Ridge (8.78 Ma at 200.92 mbsf), and more arrived in the late Miocene (5.88 Ma). The first significant quantity of sand and gravel appeared at a depth of 107.76 mbsf (4.42 Ma). Site 704, on the southern part of the Meteor Rise, received very little or no ice-rafted debris prior to 2.46 Ma. At this time, however, the greatest influx of ice-rafted debris occurred at this site. This time of maximum ice rafting correlates reasonably well with influxes of ice-rafted debris at Sites 701 (2.24 Ma) and 699 (2.38 Ma), in consideration of sample spacing at these two sites. These peaks of ice rafting may be Sirius till equivalents, if the proposed Pliocene age of Sirius tills can be confirmed. After about 1.67 Ma, the apparent mass-accumulation rate of the sediments at Site 704 declined, but with major fluctuations. This decline may be the result of a decrease in the rate of delivery of detritus from Antarctica due to reduced erosive power of the glaciers or a northward shift in the Polar Front Zone, a change in the path taken by the icebergs, or any combination of these factors.