Experimental studies of equilibria in chemically simple systems may be quantitatively extrapolated to rocks provided the activities of components in the appropriate complex phases are known. For each solid-solid equilibrium extrapolated in this way a curve of fixed Ki (equilibrium constant) for the rock may be defined in pressure-temperature space. Provided crystallization of the rock takes place under equilibrium conditions, use of two such solid-solid equilibria fixes the pressure and temperature uniquely. The relations between activities of components and mineral compositions have been determined for CaAl2SiO6-CaMgSi2O6-CaFeSi2O6 clinopyroxene and Ca3Al2Si3O12- Mg3Al2Si3O12-Fe3Al2Si3O12 garnet solid solutions. These activity-composition relations, combined with thermodynamic data on simple equilibria, were then applied to the granulites of South Harris. The equilibria used were: CaAl2Si2O8 ^ CaAl2SiO6 + SiO2, plagioclase clinopyroxene quartz CaFeSi2O6 + |Mg3Al2Si3O12 ^ clinopyroxene garnet JFe3Al2Si3O12 + CaMgSi2O6, garnet clinopyroxene 3CaAl2Si2O8 ^ Ca3Al2Si3O12 + plagioclase garnet 2Al2SiO5 + SiO2. kyanite quartz The intersection of Ki curves for appropriate mineral assemblages of the South Harris granulites yield estimated metamorphic conditions of 825 °C and 13 kbar. The calculated pressure is in excellent agreement with independent estimates (10- 13 kbar) based on the presence or absence of garnet in orthogneisses. It is concluded that, for many equilibria, the thermodynamic approach should yield pressure estimates which are accurate to within ± 1-2 kbar. Temperature uncertainties, being dependent on the slopes of Ki curves in pressure-temperature space, are related to these quoted pressure uncertainties.
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Bernard J. Wood (1977) studied this question.
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