THE ROLE OF TRACE CALCITE IN SOLUTE MASS BALANCES FROM WEATHERING OF PLUTONIC ROCKS
The present paper makes the case for the universal presence of accessory calcite based on a global suite of granitoid rocks in which calcite, determined by acid digestion and CO2, analyses, varied between 0.01 and 20 g kg-1. Calcite occurrences include small to large isolated anhedral grains, fracture and cavity fillings and sericitized cores of plagioclase. No correlation was found between calcite concentrations and bulk chemical compositions of the granitoid rocks including CaO. Petrologic literature commonly describes calcite in plutonic rocks as being secondary and originating from external sources such as hydrothermal alternation. However mineral associations, in addition to in situ 87Sr/86Sr ratios determined by ion microprobe, indicate that much of the calcite is of magmatic origin, produced by late stage cooling processes. Long-term experimental dissolution of granitic rocks (> 10 years) indicates that solute Ca and alkalinity are dominated initially by calcite dissolution in proportions related to the amount of calcite initially present. With time, calcite becomes progressively exhausted and weathering becomes dominated by slower silicate weathering. This same effect is observed for natural weathering, in which recently glaciated watersheds, such as observed by Garrels and Mackenzie for the Sierra Nevada, exhibit excess Ca and alkalinity while watersheds in geomorphically older terrains exhibit no such excesses even though the fresh granitoids contain disseminated calcite.