Monazite solubility and dissolution kinetics: implications for the thorium and light rare earth chemistry of felsic magmas

Abstract

A series of monazite dissolution experiments was conducted in a hydrous (1–6 wt.%) granitic melt at 8 kbar over the temperature range 1,000–1,400° C. A polished cube of monazite was immersed in a natural obsidian melt and allowed to partially dissolve. Electron microprobe traverses perpendicular to the crystal-melt interface revealed concentration gradients in the LREEs and P. Diffusivities of the LREEs and P were calculated from these profiles, yielding the following Arrhenius relations for the LREEs: D=0.23 exp(−60.1 kcal mol−1/RT) at 6% water D=2.30×107 exp(−122.1 kcal mol−1/RT) at 1% water These results demonstrate the importance of dissolved water on REE diffusion. Phosphorus diffusivities are nearly identical to those of the rare-earths, suggesting that P diffusion charge-compensates REE diffusion. The concentration of LREEs required for monazite saturation in these melts is given by the level of dissolved LREEs at the crystal-melt interface. These values also show a dependence on dissolved water, with LREEsat=60 ppm at 6% H2O when extrapolated down to 700° C, and LREEsat=30 ppm at 1% H2O. Calculated dissolution rates based on the above parameters indicate that minute ( 2% H2O), whereas larger (> 50 μm) crystals will likely be residual over the duration of an anatectic event. The low solubility of monazite in this melt suggests that the LREE depletion observed in some felsic differentiation suites may be the result of monazite crystallization. Limited experimental and geochemical/petrologic evidence indicates that compositional changes in the melt accompanying differentiation decrease the solubility of monazite drastically. Kinetic and chemical constraints may also lead to localized monazite saturation and inclusion in major phases or even other accessories. Variations in the REE composition of monazite from different parageneses probably reflects the REE pattern of the parent melt, and may be due to gradational differences in the stability of individual or subgroup REE-complexes as a function of melt composition. Particularly important in this regard seems to be the lime+alkali/alumina balance of the melt and its volatile content.