Melting experiments on fluorphlogopite + plagiocrase (An68) pairs have been
performed at 1 atmosphere, as a function of temperature and run duration.
Run products include, in addition to melt, spinel, forsterite and a newly f
ormed calcic plagioclase. The solidus was located between 1100 and 1150 deg
rees C and the amount of melt produced increases sharply at 1200 degrees C.
From this temperature, liquids are compositionally zoned between the two m
ineral interfaces, and the mica reacts out after sufficient time indicating
the existence of a critical temperature of melting located between 1175 an
d 1200 degrees C. These two temperature domains are also characterized by d
ifferences in plagioclase reaction textures, melt proportions and reaction
rates.
Textural and Sr isotopic studies of the plagioclases show that at all tempe
ratures the first step of the melting reaction is characterized by congruen
t dissolution of the starting plagioclase followed by precipitation of the
new plagiocrase. At ail temperatures the melt compositions are initially lo
cated on the intersection of the cotectic line and the starting plagioclase
-fluorphlogopite tie line. Below the critical temperature of melting these
melts are metastable undercooled liquids. Above the critical temperature of
melting there is an array of stable melt compositions located on the plagi
oclase-fluorphlogopite tie-line. In both cases the melt compositions evolve
with time toward more albite-rich compositions in conjunction with the new
plagioclase precipitation. The system fluorphlogopite-plagioclase thus pro
vides an example where liquid compositions vary with time although plagiocl
ase-melt interface equilibrium is satisfied. This is due to the involvement
of a solid solution in the reaction.
Above the critical temperature of melting, the rate-controlling process for
melting is chemical diffusion in the melt. Below the critical temperature
of melting the rate-limiting step is the formation of the metastable underc
ooled melt. The sluggishness of the melting reaction in this temperature re
gime is explained by the difficulty of forming such a melt.