MODELLING CLINOPYROXENE-GARNET AMPHIBOLITE ASSEMBLAGES AT MICA CREEK, BRITISH COLUMBIA: THE ROLE OF THE FLUID PHASE
Phase diagram sections constructed in the chemical system TiO2-Na2O-CaO-FeO-MgO-Al2O3-SiO2-H2O illustrate the effect of H2O activity and H2O bulk rock content on predicted equilibria for a Grt- Cpx- hornblende (Hb)- Pl- titanite (Ttn)- ilmenite (Ilm)- Qtz amphibolite bulk rock composition. The activity of H2O has to be < 0.5 to obtain the assemblage at amphibolite facies conditions. Evidence for a very reduced activity of H2O in a fluid phase is lacking. Isobaric temperature-composition sections (bulk-rock H2O) indicate that at low bulk-rock H2O contents (fluid phase absent), a Grt- Cpx- Hb- Pl- Ilm- Qtz assemblage can develop at amphibolite facies conditions. The models do not predict a stability field for Ttn + Cpx as observed in the rock. A reduced H2O activity section at an H2O activity of 0.5 predicts the stable univariant equilibrium 52 Amp + 48 Ilm + 75 Qtz + 148 Ttn=25 Grt + 10 Pl + 242 Cpx + 196 rutile + 52 H2O from 8.7 - 8.9 kilobars, 700 - 690 C, along which Cpx reacts into and Ttn reacts out of the assemblage for this bulk rock composition. The bulk-rock H2O sections require pressures > 9 kilobars for Ttn stability. The observed modes compared to those predicted by the reduced H2O activity and bulk-rock H2O sections suggest the sections overestimate modal garnet and underestimate modal clinopyroxene.