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The influence of the fluid phase composition on the solidus temperatures in the haplogranite system NaAlSi3O8-KAlSi3O8-SiO2-H2O-CO2
Authors:Hans Keppler
Institution:(1) Mineralogisches Institut der Universität, Kaiserstrasse 12, 7500 Karlsruhe, Germany;(2) Present address: Division of Geological and Planetary Sciences 170-25, California Institute of Technology, 91125 Pasadena, California, USA
Abstract:The solidus temperatures in the haplogranite-system NaAlSi3O8-KAlSi3O8-SiO2-H2O-CO2 have been determined up to 15 kbar for a constant molar ratio of sodium to potassium of 1ratio1 and for fluid compositions ranging from pure water to pure carbon dioxide. The data for the water-saturated solidus are virtually identical with those of previous studies. At constant pressure, the solidus curve as a function of the fluid phase composition exhibits a point of inflection in the range of the water-rich compositions. This phenomenon is attributed to chemical interactions between the CO2 and the H2O in the silicate melt. The point of inflection disappears if the CO2 in the gas phase is replaced by molecular nitrogen. The CO2-saturated solidi have been measured at 2 and 5 kbars. The data at 5 kbar indicate a melting point depression in the order of 40° C compared to the dry solidus of Huang and Wyllie (1975). The experimental data can be used to estimate the melting temperatures of common quartz and feldspar bearing crustal rocks under the conditions of granulite facies metamorphism. Since for most fluid phase compositions, the solidus curves are very steep in the P, T-diagram, the beginning of melting is nearly exclusively determined by the fluid composition and almost independent of pressure between about 2 and more than 10 kbar. Therefore, the onset of partial melting in quartz and feldspar containing rocks under granulite facies conditions can be used to estimate the composition of a coexisting H2O-CO2 fluid phase if geothermometric data are available. The temperature range between the beginning of granulite facies metamorphism and the initiation of melting expands with increasing carbon dioxide content in the H2O-CO2 fluid phase. At a CO2 molar fraction of 0.9, this range extends from about 600° C to 900° C and is almost independent of pressure.
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