Solute fluxes from a glacier-covered alpine catchment are partitioned
into components derived from sea salt, acid aerosol, dissolution of at
mospheric CO2, and crustal weathering. The bulk of solute is crustally
derived. Coupled sulfide oxidation and carbonate dissolution (SO-CD)
and carbonation of carbonate minerals generate approximately equal amo
unts of solute. Chemical denudation constitutes <1.5% of solid denudat
ion but is significantly higher than the continental average. CO2 draw
down by weathering reactions varies directly with discharge and suspen
ded-sediment load and inversely with meltwater p(CO2). If it is genera
lly true that flushing rates control CO2 drawdown in glacier-covered c
atchments, then glacially driven chemical weathering could be a signif
icant factor in carbon cycling and climate change on glacial-interglac
ial time scales.