POLY-MINERAL CRYSTAL SIZE DISTRIBUTIONS: IMPORTANT CLUES TO METAMORPHIC RATES AND PROCESSES ALONG SEGMENTS OF PRESSURE-TEMPERATURE-TIME PATHS
Parameters that interact with P,T and t to determine CSD in metamorphic rocks are the reaction affinity (A), the effective diffusion coefficient (D), and the distribution of previously formed phases in the rock. A controls the nucleation rate, D governs the size of equilibration volumes that form around minerals to inhibit nucleation, and the distribution of previously formed minerals determines how A is locally buffered by the metastable assemblage for a given D.
Both A and D are sensitive to the tectonic environment that controls dT/dt and dP/dt. Over stepping a reaction changes A, which depends on dT/dt & dP/dt imposed by tectonics, and the dT/dP of the equilibrium reaction. For constant D, larger A produces a higher nucleation rate and smaller crystal sizes. The major control on D depends on the amount of fluid along the grain boundaries: D in dry rocks is several orders of magnitude smaller than D in wet rocks. Thermally dominated regional PT path segments (large dT/dP) in metapelites form big porphyroblasts or segregations because they cross dehydration reactions that wet grain boundaries, greatly increasing D. Conversely, decompression dominated prograde PT path segments (small positive dT/large negative dP) in metapelites can produce many small crystals because of rehydration reactions that dry out grain boundaries, lowering D so that domains of equilibrium have small volumes when the new minerals nucleate and begin to grow.