Biotite is a particularly important mineral in metamorphic rocks because of its occurrence not only in nature over a wide range of bulk compositions and metamorphic grades, but also computationally in numerous equilibria that represent useful thermobarometers and boundaries on petrogenetic grids. In spite of its obvious importance, quantitative calculations involving biotite continue to be relatively uncertain, as evidenced by major differences in computed petrogenetic grids for metapelites (e.g., Spear and Cheney 1989;Powell and Holland 1990;Pattison and Tracy 1991;Xu et al. 1994) and thermobarometric formulations involving biotite (e.g., Ferry and Spear 1978;Perchuk and Lavrent!eva 1983;Aranovich et al. 1988;Holdaway et al. 1997
ABSTRACTThe stability of Mg-Fe-Al biotite has been investigated with reversed phase-equilibrium experiments on four equilibria. Experimental brackets in pure H 2 O and H 2 O-CO 2 mixtures for the equilibrium:phlogopite + 3 quartz = enstatite + sanidine + H 2 O( 1) are in good agreement with previous experiments in mixed-volatile ß uids (Bohlen et al. 1983) and H 2 O-KCl solutions (Aranovich and Newton 1998), while indicating a reduced stability Þ eld for phlogopite compared to previous data in pure H 2 O (Wood 1976;Peterson and Newton 1989). Aluminum solubility in biotite has been determined in the Fe-, Mg-, and Fe-Mg systems from reversed phase-equilibrium data for the equilibria: