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Controlling factors of volumetrically important marine carbonate cementation in deep slope settings 总被引：1，自引：0，他引：1
BRAM VAN DER KOOIJ ADRIAN IMMENHAUSER THOMAS STEUBER JUAN RAMON BAHAMONDE RIONDA OSCAR MERÍNO TOMÉ 《Sedimentology》2010,57(6):1491-1525
The controlling parameters of early marine carbonate cementation in shoal water and hemipelagic to pelagic domains are well‐studied. In contrast, the mechanisms driving the precipitation of early marine carbonate cements at deeper slope settings have received less attention, despite the fact that considerable volumes of early marine cement are present at recent and fossil carbonate slopes in water depths of several hundreds of metres. In order to better understand the controlling factors of pervasive early marine cementation at greater water depths, marine carbonate cements observed along time‐parallel platform to basin transects of two intact Pennsylvanian carbonate slopes are compared with those present in the slope deposits of the Permian Capitan Reef and Neogene Mururoa Atoll. In all four settings, significant amounts of marine cements occlude primary pore spaces downslope into thermoclinal water depths, i.e. in a bathymetric range between some tens and several hundreds of metres. Radial, radiaxial and fascicular optic fibrous calcites, and radiaxial prismatic calcites are associated with re‐deposited facies, boundstones and rudstones. Botryoidal (formerly) aragonitic precipitates are common in microbially induced limestones. From these case studies, it is tentatively concluded that sea water circulation in an extensive, near‐sea floor pore system is a first‐order control on carbonate ion supply and marine cementation. Coastal upwelling and internal or tidal currents are the most probable mechanisms driving pore water circulation at these depths. Carbonate cements precipitated under conditions of normal to elevated alkalinity, locally elevated nutrient levels and variable sea water temperatures. The implications of these findings and suggestions for future work are discussed. 相似文献
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J. A. PADRÓN‐NAVARTA C. J. GARRIDO A. SÁNCHEZ‐NAVAS A. TOMMASI V. LÓPEZ SÁNCHEZ‐VIZCAÍNO M. T. GÓMEZ‐PUGNAIRE S. S. HUSSAIN 《Journal of Metamorphic Geology》2008,26(8):855-870
Garnet growth in high‐pressure, mafic garnet granulites formed by dehydration melting of hornblende‐gabbronorite protoliths in the Jijal complex (Kohistan palaeo‐island arc complex, north Pakistan) was investigated through a microstructural EBSD‐SEM and HRTEM study. Composite samples preserve a sharp transition in which the low‐pressure precursor is replaced by garnet through a millimetre‐sized reaction front. A magmatic foliation in the gabbronorite is defined by mafic‐rich layering, with an associated magmatic lineation defined by the shape‐preferred orientation (SPO) of mafic clusters composed of orthopyroxene (Opx), clinopyroxene (Cpx), amphibole (Amp) and oxides. The shape of the reaction front is convoluted and oblique to the magmatic layering. Opx, Amp and, to a lesser extent, Cpx show a strong lattice‐preferred orientation (LPO) characterized by an alignment of [001] axes parallel to the magmatic lineation in the precursor hornblende‐gabbronorite. Product garnet (Grt) also displays a strong LPO. Two of the four 〈111〉 axes are within the magmatic foliation plane and the density maximum is subparallel to the precursor magmatic lineation. The crystallographic relationship 〈111〉Grt // [001]Opx,Cpx,Amp deduced from the LPO was confirmed by TEM observations. The sharp and discontinuous modal and compositional variations observed at the reaction front attest to the kinetic inhibition of prograde solid‐state reactions predicted by equilibrium‐phase diagrams. The P–T field for the equilibration of Jijal garnet granulites shows that the reaction affinities are 5–10 kJ mol.?1 for the Grt‐in reaction and 0–5 kJ mol.?1 for the Opx‐out reaction. Petrographic and textural observations indicate that garnet first nucleated on amphibole at the rims of mafic clusters; this topotactic replacement resulted in a strong LPO of garnet. Once the amphibole was consumed in the reaction, the parallelism of [001] axes of the mafic‐phase reactants favoured the growth of garnet crystals with similar orientations over a pyroxene substrate. These aggregates eventually sintered into single‐crystal garnet. In the absence of deformation, the orientation of mafic precursor phases conditioned the nucleation site and the crystallographic orientation of garnet because of topotaxial transformation reactions and homoepitaxial growth of garnet during the formation of high‐pressure, mafic garnet‐granulite after low‐pressure mafic protoliths. 相似文献
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