996 resultados para Prairie States Forestry Project (U.S.)


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Shear-wave and compressional-wave velocities of 26 basalt samples collected at Site 504 during Deep Sea Drilling Project Legs 69 and 70 were measured at elevated confining pressures. The young basalts have higher velocities than average DSDP basalts, because of their lack of alteration. Measurements of sample porosity are combined with laboratory and in situ velocity measurements to yield estimates of total crustal porosity: 13% at the top of Layer 2, and very low porosity below a depth of 2.0 km.

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An Eocene-Oligocene oxygen and carbon isotope history based on planktonic and benthic foraminifers from Deep Sea Drilling Project Leg 71 cores has been constructed for the Maurice Ewing Bank of the eastern Falkland Plateau, Southwest Atlantic Ocean. Specifically, the cores cover portions of the middle Eocene, upper Eocene, and lower Oligocene. Surface water isotopic temperatures postulated for the middle Eocene at Site 512 fluctuated within about four degrees but generally averaged about 9°C. Bottom isotopic temperatures at Site 512 (water depth, 1846 m) were generally a degree lower than surface water temperatures. Surface water isotopic temperatures at Site 511 initially averaged about 11°C during the late Eocene, but dropped to an average of 7°C in the early Oligocene. Bottom isotopic temperatures at Site 511 (water depth, 2589 m) generally record temperatures between 12.5°C and 8°C, similar to the range in the surface water isotopic temperatures. During the early Oligocene, bottom isotopic temperatures dropped sharply and averaged about 2°C (very close to present-day values). Surface water temperature values also decreased to an average of about 7°C, therefore leading to a significant divergence between surface and bottom water isotopic temperatures during the early Oligocene. Comparisons among Southern Ocean DSDP Sites 511, 512, and 277, and between these and other DSDP sites from central and northern latitudes (Sites 44, 167, 171, 292, 357, 398, 119, and 401) show that much of the Eocene was characterized by relatively warm temperatures until sometime in either the middle Eocene, late Eocene, or early Oligocene. At each site, conspicuous 18O enrichments occur in both the benthic and planktonic foraminifers over a relatively short period of time. Although a general trend toward a climatic deterioration is evident, the density of data points among the various studies is still too sparse to determine either synchrony or time-transgression between the major isotopic events. A close correlation could be made between the Site 511 oxygen isotope temperature curve and paleoclimatic trends derived independently from radiolarian studies. The sharp temperature drop and the divergence between bottom and surface water temperatures during the early Oligocene apparently reflect a major expansion of the antarctic water mass. The migration of the boundary between the subantarctic and antarctic water masses over the site at this time would account in part for the sharp temperature changes. Sharp changes of this nature would not necessarily be noted in other geographic areas, particularly those to the north which have different oceanographic regimes.

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About 200 volcanic ash layers were recovered during DSDP Leg 57. The volcanic glass in some of these layers was investigated petrographically and chemically in this study. Volcanic glass is mainly rhyolitic and/or rhyodacitic in chemical composition, and its refractive index ranges from 1.496 to 1.529. Some volcanic ash layers consist of multiple grains of different chemical compositions. All the volcanic glass belongs to the tholeiitic and the calc-alkalic volcanic rock series, in SiO2-(Na2O + K2O) diagram and FeO*/MgO-SiO2 diagram. We correlated successfully three volcanic ash layers from the standpoint of chemical composition and biostratigraphy. Hydration of volcanic glass from Leg 57 is less intense than in other DSDP cores.

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Seventeen whole-rock samples, generally taken at 25- to 50-meter intervals from 5 to 560 meters sub-basement in Deep Sea Drilling Project Hole 504B, were analyzed for 87Sr/86Sr ratios, and rubidium and strontium concentrations. Ten of these samples also were analyzed for Pb-isotope composition. Strontium-isotope ratios for eight samples from the upper 260 meters of the hole range from 0.70287 to 0.70377, with a mean of 0.70320. In the interval 330 to 560 meters, five samples have a restricted range of 0.70259 to 0.70279, with a mean of 0.70266, almost identical to the average value of fresh mid-ocean-ridge basalts. In the interval 260 to 330 meters, approximately intermediate strontium- isotope ratios are found. The higher 87Sr/86Sr ratios in the upper part of the hole can be interpreted in terms of strontium-isotope alteration during basalt-sea-water interaction. Relative to average fresh mid-ocean ridge basalts, the upper 260 meters of basalts are enriched by an average of about 9% in sea-water strontium 87Sr/86Sr = 0.7091). This Sr presumably is located in the smectites, which, as the main secondary minerals throughout the hole, replace olivine and matrix glass and locally fill vesicles (analyzed samples contained no veins). The strontium-isotope data strongly suggest that the integrated flux of sea water through the upper part of the Hole 504B crust has been greater than through the lower part. This is also suggested by (1) the common occurrence of Feoxide- hydroxide minerals as alteration products above 270 meters, but their near absence below 320 meters, (2) the presence of vein calcite above 320 meters, but its near absence below this level, and (3) the occurrence of vein pyrite only below a depth of 270 meters. Sea-water circulation in the lower basalts may have been partly restricted by the greater number of relatively impermeable massive lava flows below 230 meters sub-basement. Although sufficient sea water was present within the lower part of the hole to produce smectitic alteration products, the overall water /rock ratio was low enough to prevent significant modification of strontium-isotope ratios. Lead-isotope ratios of Hole 504B basalts form approximately linear arrays in plots of 208Pb/204Pb and 207Pb/204Pb versus 206Pb/204Pb. The arrays are similar to those reported for basalts from other mid-ocean ridges. There is no trend in Hole 504B lead-isotope ratios with vertical position in the basement. The arrays indicate that the lead-isotope composition of the upper mantle from which the Hole 504B basaltic melts were derived was inhomogeneous.

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Precise velocity and density measurements at atmospheric and elevated pressures have been obtained on basalts drilled in 13 holes during Leg 54. The vp-sigma data show systematics which are controlled by the degree of crystallinity (or conversely, glassiness), microstructure, and original mineralogy and chemistry. Extensively fractionated basalts with marked iron enrichment produce anomalously low measured velocities at densities above 2.90 g/cm**3. Also, the effective in situ pressure acting on Leg 54 basalts is less than hydrostatic, and perhaps close to zero. At zero effective pressure, the measured velocities average 2.5 km/s higher than East Pacific Rise upper crustal velocities determined by seismic refraction. This implies that the in situ velocities are undoubtedly a result of the highly fragmented nature of East Pacific Rise crust.

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The major magnetic mineral in the turbidites and slumped sediments recovered at Leg 73 drill sites was near to magnetite in composition and in the form of small multidomain particles. There was no variation in magnetic mineralogy with the lithology. The variations in the intensities and directions of the natural remanent magnetization could be explained in terms of postdepositional grain rotations within the wet sediment. In the sands realignment was partial, whereas in some of the slumps the entire remanent magnetization was reset. Fine-particle magnetite was also the main magnetic constituent of the red clays. A significant proportion of a higher-coercivity mineral was also present. The magnetic characteristics of the red clays are explained as a combination of concentration and grain rotation effects. The implications to the assessment of the reliability of paleomagnetic data are discussed. Note: Conversion factors are as follows: 1 Am**2/kg = 1 emu/g, and 80 A/m about 1 Oe.