摘要
High-grade dehydration of amphibolite-facies rocks to granulite-facies is a process that can involve partial melting, fluid-aided solid-state dehydration, or varying degrees of both. On the localized meter scale, solid-state dehydration, due to CO：-rich fluids traveling along some fissure or crack and subsequently outwards along the mineral grain boundaries of the surrounding rock, normally is the means by which the breakdown of biotite and amphibole to orthopyroxene and clinopyroxene occur. Various mineral textures and changes in mineral chemistry seen in these rocks are also seen in more regional orthopyroxene-clinopyroxene-bearing rocks which, along with accompanying amphibolite-facies rocks, form traverses of lower crust. This suggests that solid-state dehydration during high-grade metamorphism could occur on a more regional scale. The more prominent of these fluid-induced textures in the granulite- facies portion of the traverse take the form of micro-veins of K-feldspar along quartz grain boundaries and the formation of monazite inclusions in fluorapatite. The fluids believed responsible take the form of concentrated NaCl- and KCl- brines from a basement ultramafic magma heat source traveling upwards along grain boundaries. Additional experimental work involving CaSO4 dissolution in NaCl-brines, coupled with natural observation of oxide and sulfide mineral associations in granulite-facies rocks, have demonstrated the possibility that NaCl-brines, with a CaSO4 component, could impose the oxygen fugacity on these rocks as opposed to the oxygen fugacity being inherent in their protoliths. These results, taken together, lend credence to the idea that regional chemical modification of the lower crust is an evolutionary process controlled by fluids migrating upwards from the lithospheric mantle along grain boundaries into and through the lower crust where they both modify the rock and are modified by it.Their presence allows for rapid mass and heat transport and subsequent mineral genesis and mineral re- equilibration in the rocks through which they pass.
High-grade dehydration of amphibolite-facies rocks to granulite-facies is a process that can involve partial melting, fluid-aided solid-state dehydration, or varying degrees of both. On the localized meter scale, solid-state dehydration, due to CO：-rich fluids traveling along some fissure or crack and subsequently outwards along the mineral grain boundaries of the surrounding rock, normally is the means by which the breakdown of biotite and amphibole to orthopyroxene and clinopyroxene occur. Various mineral textures and changes in mineral chemistry seen in these rocks are also seen in more regional orthopyroxene-clinopyroxene-bearing rocks which, along with accompanying amphibolite-facies rocks, form traverses of lower crust. This suggests that solid-state dehydration during high-grade metamorphism could occur on a more regional scale. The more prominent of these fluid-induced textures in the granulite- facies portion of the traverse take the form of micro-veins of K-feldspar along quartz grain boundaries and the formation of monazite inclusions in fluorapatite. The fluids believed responsible take the form of concentrated NaCl- and KCl- brines from a basement ultramafic magma heat source traveling upwards along grain boundaries. Additional experimental work involving CaSO4 dissolution in NaCl-brines, coupled with natural observation of oxide and sulfide mineral associations in granulite-facies rocks, have demonstrated the possibility that NaCl-brines, with a CaSO4 component, could impose the oxygen fugacity on these rocks as opposed to the oxygen fugacity being inherent in their protoliths. These results, taken together, lend credence to the idea that regional chemical modification of the lower crust is an evolutionary process controlled by fluids migrating upwards from the lithospheric mantle along grain boundaries into and through the lower crust where they both modify the rock and are modified by it.Their presence allows for rapid mass and heat transport and subsequent mineral genesis and mineral re- equilibration in the rocks through which they pass.
