NATURAL "SEQUESTRATION" OF ATMOSPHERIC CARBON BY WEATHERING OF KENTUCKY'S CARBONATE MINERALS
The ratio of TIC derived from "old" mineral carbon to that from "young" atmospheric carbon of 57:43 is in contrast to published estimates of continental carbonate mineral weathering CO2 sink terms that have typically assumed that each mole of old mineral carbon reacts with one mole of young carbon as H2CO3* for a 50:50 ratio. Examination of the kinetics of the CaCO3-H2O-CO2 system suggests that details of atmospheric CO2/carbonate mineral interactions may have some dependence on the kinetics of the dissolution and precipitation reactions. The often-assumed overall balance between the continental CO2 sink (from weathering of carbonate minerals) and the oceanic CO2 source (from an equal amount of carbonate mineral precipitation) may thus not be in balance to the extent that the kinetics of the reactions are influenced by varying geochemical environments.
We are currently 1) collecting data at several locations in Kentucky during 2001-02 to add organic carbon fluxes to our model, and to quantitatively evaluate impact of strong acids, and 2) expanding our carbon dynamics monitoring network to California (alpine) and southern China (subtropical) to begin to understand climatic influences on these processes.