1000 resultados para Newlands Project (U.S.)


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During the Leg 67 drilling of the Middle America Trench (Guatemala transect), basalts were reached in Hole 495, 22 km seaward from the Trench axis, in Holes 500 and 500B at the foot of the continental slope, and at four other holes not sampled for this study. Only olivine-plagioclase phyric basalts are present in Hole 495, whereas in Holes 500 and 500B these rocks are associated with plagioclase phyric high-alumina basalts. As illustrated by the content of TiO2, Al2O3, and the K2O/K2O + Na2O ratio, some of the Middle America Trench basalts do not differ essentially from oceanic tholeiites, but others have a composition transitional to island-arc tholeiitic basalts. It is suggested that basalts transitional from oceanic to island-arc tholeiites are typical manifestations of magmatism in zones of convergence of the oceanic and continental or island-arc crust.

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Sediments in the area of the Galapagos hydrothermal mounds are divided into two major categories. The first group, pelagic sediments, are nannofossil oozes with varying amounts of siliceous microfossils. The second group are hydrothermal sediments consisting of manganese-oxide crust fragments and green nontronitic clay granules. Hydrothermal sediments occur only in the upper half to two-thirds of the cores and are interbedded and mixed with pelagic sediments. Petrologic evidence indicates that hydrothermal nontronite forms as both a primary precipitate and as a replacement mineral of pre-existing pelagic sediment and hydrothermal manganese-oxide crust fragments. In addition, physical evidence supports chemical equations indicating that the pelagic sediments are being dissolved by hydrothermal solutions. The formation of hydrothermal nontronite is not merely confined to the surface of mounds, but also occurs at depth within their immediate area; hydrothermal nontronite is very likely forming today. Geologically speaking, the mounds and their hydrothermal sediments form almost instantaneously. The Galapagos mounds area is a unique one in the ocean basins, where pelagic sediments can be diagenetically transformed, dissolved, and replaced, possibly within a matter of years.

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We report here chemical analyses of sulfide and other minerals occurring in the massive sulfide deposit cored at Site 471. Details of the mineralogy and inferred paragenesis of the deposit will be reported elsewhere. The sulfide deposit at Site 471 occurs between overlying pelagic sediment and underlying basalt. The deposit is vertically zoned and consists, from top to bottom, of the following mineral assemblages: (1) pyrite, chalcopyrite, and Zn-sulfide in chert and calcite gangue (about 35 cm thick); (2) a 5-cm-thick metalliferous sediment layer described in detail by Leinen (this volume); and (3) a 4-cm-thick chert layer. The overlying sediment is a calcareous silty claystone that contains middle Miocene coccoliths (Bukry, this volume). The underlying basalt has been extensively chloritized and veined with calcite. In places feldspars are albitized, and calcite occurs as pseudomorphs after olivine. Relict textures suggest that the basalt grades into diabase and gabbro with increasing depth. Neither stock work nor disseminated sulfides was observed in the altered rocks.

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CaCO3 content was determined on board ship by the "Karbonat Bomb" technique (Müller and Gastner, 1971). In this simple procedure, a sample is powdered and treated with HCl in a closed cylinder. Any resulting CO2 pressure is proportional to the CaCO3 content of the sample. Application of the calibration factor to the manometer reading (x 100) yields per cent CaCO3. The error can be as low as 1 per cent for sediments high in CaCO3, and in general an accuracy of ±2 to 5 per cent can be obtained.