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* Institute for Mineralogy and Petrology, ETH Zürich, Zürich 8092, Switzerland
** Research School of Earth Sciences, The Australian National University, Canberra, ACT 0200, Australia
Department of Earth and Marine Sciences, The Australian National University, Canberra, ACT 0200, Australia
Corresponding author: alistair.hack{at}erdw.ethz.ch
Phase relations involving hydrous melting, volatile and mineral solubility and supercritical fluid phenomena at high pressure for mineral–H2O systems are generally not completely constrained by experimental data or adequately treated in thermodynamic models. Here we examine geometric relations in pressure (P)-temperature (T)-composition (X) topologies of simple hydrous A–H2O binaries, thus avoiding some of the pitfalls associated with other approaches. The relations between mineral solubility surfaces, wet melting and critical L=V behavior are shown explicitly in a series of PT, TX and isopleth contoured PT projections. Our analysis highlights the significance of Clapeyron slopes of melt- and fluid-solubility isopleths for L+V coexistence, supercritical-fluid phenomena and the geometry of phase-equilibrium boundaries. The results are useful for understanding wet melting, magma degassing and fluid behavior in high-pressure metamorphic and subduction-zone environments. The diagrams illustrate the general pattern of mineral solubility in aqueous fluids and volatile solubility in silicate melts. We discuss the significance of the critical-curve geometry for phase relations and fluid/melt densities. We examine a continuum of phase relation topologies for A–H2O, and show that these can result from subtle but important differences in the compositional behavior of melt coexisting with H2O-rich fluid. The systems SiO2(quartz)–H2O and NaAlSi3O8(albite)–H2O are taken as examples for which there is experimental data available to calibrate a complete phase relation topology.
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