Solute acquisition by Alpine glacial meltwaters is the result of the c
oupling of different pairs of reactions, one of which usually involves
dissolved gases. Hence, the availability of atmospheric gases to solu
tion is an important control on the composition of glacial meltwaters.
The chemical compositions of the two main components of the bulk melt
water, quick flow and delayed flow, are dominated by different geochem
ical processes. Delayed flow waters are solute-rich and exhibit high p
(CO2) characteristics. The slow transit of these waters through a dist
ributed drainage system and the predominance of relatively rapid react
ions, such as sulphide oxidation and carbonate dissolution, in this en
vironment maximize solute acquisition. Quick-flow waters are dilute, b
oth because of their rapid transit through ice-walled conduits and ope
n channels, and because the weathering reactions are fuelled by relati
vely slow gaseous diffusion of CO2 into solution, despite solute acqui
sition being dominated by rapid surface exchange reactions. As a conse
quence, quick flow usually bears a low or open-system p(CO2) signature
. Bulk meltwaters are more likely to exhibit low p(CO2) values when su
spended-sediment concentrations are high, which promotes post-mixing r
eactions. This conceptual model suggests that the composition of both
quick flow and delayed flow is likely to be temporally variable, since
kinetic, rather than equilibrium, factors determine the composition.