930 resultados para Biocatalysis at Moderate Pressures


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We present results of a microprobe investigation of fresh and least-deformed and metamorphosed gabbroic rocks from Leg 118, Hole 735B, drilled on the east side of the Atlantis II Fracture Zone, Southwest Indian Ridge. This rock collection comprises cumulates ranging from troctolites to olivine-gabbro and olivine-gabbronorite to ilmenite-rich ferrogabbros and ferrogabbronorites. As expected, the mineral chemistry is variable and considerably expands the usual oceanic reference spectrum. Olivine, plagioclase, and clinopyroxene are present in all the studied samples. Orthopyroxene and ilmenite, although not rare, are not ubiquitous. Olivine compositions range from Fo85 to Fo30, while plagioclase compositions vary from An70 to An27. Mg/(Mg + Fe2+) of clinopyroxene (mostly diopside to augite) varies from 0.88 to 0.54. Mg/(Mg + Fe2+) of orthopyroxene varies from 0.84 to 0.50. These minerals are not significantly zoned. All mineralogical data indicate that fractional crystallization is an important factor for the formation of cumulates. However, sharp contacts, interpreted as layering boundaries or intrusion margins, suggest polycyclic fractionation of several magma batches of limited volumes. Calculated compositions of magmas in equilibrium with the most magnesian mineral samples at the bottom of the hole represent fractionated liquids through separation of olivine, plagioclase, and clinopyroxene at moderate to low pressures (less than 9 kb). Crystallization of orthopyroxene and ilmenite occurs in the most differentiated liquids. Mixing of magmas having various compositions before entering the cumulate zone is another mechanism necessary to explain extremely differentiated iron-rich gabbros formed in this slow-spreading ridge environment.

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This study investigates abundance variations in Noelaerhabdaceae assemblages during the late Oligocene-early Miocene at three subtropical sites in the Atlantic and Pacific oceans (DSDP Sites 516, 608 and 588). At these three sites, nannofossil assemblages were characterized by the successive high proportion of Cyclicargolithus, Dictyococcites and Reticulofenestra. Local paleoceanographic changes, such as the input of nutrient-poor water masses, might explain shifts in ecological prominence within the Noelaerhabdaceae at DSDP Site 516 (South Atlantic). But the similar timing of a decline in Cyclicargolithus at the three studied sites more likely corresponds to a global process. Here, we explore possible causes for this long-term taxonomic turnover. A global change in climate, associated with early Miocene glaciations, could have triggered a decline in fitness of the taxon Cyclicargolithus. The ecological niche made vacant because of the decrease in Cyclicargolithus could then have been exploited by Dictyococcites and Reticulofenestra that became prominent in the assemblages after 20.5 Ma. Alternatively, this global turnover might reflect a gradual evolutionary succession and be the result of other selection pressures, such as increased competition between Cyclicargolithus and Dictyococcites/Reticulofenestra. A diversification within Dictyococcites/Reticulofenestra, indicated by an expansion in the size variation within this group since ~ 20.5 Ma, may have contributed to the decreased fitness of Cyclicargolithus.

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Experimental phase relations were used to assess the role of volatiles and crustal level fractional crystallization in the petrogenesis of lavas from Hole 839B in the central Lau Basin. Melting experiments were performed on Sample 135-839B-15R-2, 63-67 cm, at 1 atm, anhydrous, and 2 kbar, H2O-saturated (~6 wt% H2O in the melt) to determine the influence of variable pressure and H2O content on phase appearances, mineral chemistry, and liquid line of descent followed during crystallization. The effects of H2O are to depress the liquidus by ~100°C, and to suppress crystallization of plagioclase and orthopyroxene relative to olivine and high-Ca clinopyroxene. At 1 atm, anhydrous, olivine and plagioclase coexist near the liquidus, whereas orthopyroxene and then clinopyroxene appear with decreasing temperature. Crystallization of 50 wt% produces a residual liquid that is rich in FeO* (10.8 wt%) and poor in Al2O3 (13.6 wt%). At 2 kbar, H2O-saturated, the liquidus phases are olivine and chromian spinel, with high-Ca clinopyroxene appearing after ~10% crystallization. Plagioclase saturation is suppressed until ~20% crystallization has occurred. The residual liquid from 35 wt% crystallization is rich in AI2O3 (17.4 wt%), and poor in MgO (4.82 wt%); it contains moderate FeO* (8.2 wt%), and resembles the low-MgO andesites recovered from Hole 839B. On the basis of these experiments we conclude that the primitive lavas recovered from Hole 839B have experienced crystallization along the Ol + Cpx saturation boundary, under hydrous conditions (an ankaramitic liquid line of descent), and variable amounts of olivine and chromian spinel accumulation. The low-MgO andesites from Hole 839B are the products of hydrous fractional crystallization, at crustal pressures, of a parent magma similar to basaltic andesite Sample 135-839B-15R-2, 63-67 cm.

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The Deep Sea Drilling Project, in addition to providing valuable information on the history and processes of development of the ocean, has significantly contributed to our knowledge of the chemical and physical nature of the upper oceanic crust. Among the important physical properties of the crust are its seismic velocity and structure, the interpretation of which requires laboratory studies of seismic velocities in oceanic rocks.

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The Integrated OceanDrilling Program's Expedition 302, the Arctic Coring Expedition (ACEX), recovered the first Cenozoic sedimentary sequence from the central Arctic Ocean. ACEX provided ground truth for basin scale geophysical interpretations and for guiding future exploration targets in this largely unexplored ocean basin. Here, we present results from a series of consolidation tests used to characterize sediment compressibility and permeability and integrate these with high-resolution measurements of bulk density, porosity and shear strength to investigate the stress history and the nature of prominent lithostratigraphic and seismostratigraphic boundaries in the ACEX record. Despite moderate sedimentation rates (10-30 m/Myr) and high permeability values (10**-15 -10**-18 m**2), consolidation and shear strength measurements both suggest an overall state of underconsolidation or overpressure. One-dimensional compaction modelling shows that to maintain such excess pore pressures, an in situ fluid source is required that exceeds the rate of fluid expulsion generated by mechanical compaction alone. Geochemical and sedimentological evidence is presented that identifes the Opal A-C/T transformation of biosiliceous rich sediments as a potential additional in situ fluid source.However, the combined rat of chemical and mechanical compaction remain too low to fully account for the observed pore pressure gradients, implying an additional diagenetic fluid source from within or below the recovered Cenozoic sediments from ACEX. Recognition of the Opal A-C/T reaction front in the ACEX record has broad reaching regional implications on slope stability and subsurface pressure evolution, and provides an important consideration for interpreting and correlating the spatially limited seismic data from the Arctic Ocean.