EFFECTS OF SURFACE WATER AND GROUNDWATER INTERACTION ON ARSENIC CYCLING IN THE DATONG BASIN, CHINA: RESULTS FROM ONE-YEAR MONITORING
On the basis of the As concentration data and previous hydrochemical and sediment analysis, we hypothesize the potential mechanisms for observed As concentration variations. The river water recharges the groundwater during peak flows and flooding. Additional oxygen (O2) is carried into the aquifers and it reacts rapidly with existing Fe2+ in the groundwater to produce Fe3+. The weakly alkaline condition promotes formation of Fe(OH)3. Consequently, As concentrations decrease as As is incorporated into newly formed Fe(OH)3 via surface-adsorption and/or co-precipitation. In addition, O2 also reacts with As-bearing Fe(II) sulfides, which allows release of As into the groundwater and leads to sharp rises of As concentration. This reaction also generates Fe2+ and more Fe(OH)3 and As surface-adsorption on and/or co-precipitation with Fe(OH)3 occurs. Consequently, As concentration declines.
When the flooding recedes, the additional O2 inputs diminish. The reducing environments prevail in aquifers. Possible microbial reduction dissolution of newly formed Fe(OH)3 dominates As mobilization in the groundwater and releases Fe2+ and As. Therefore, gradual increases in As concentration were observed. Additionally, newly formed Fe2+ reacts with S2- and Fe(II) sulfides form. Fe(II) sulfides can immobilize As via surface-adsorption and/or co-precipitation, which decreases As concentration in the groundwater. When surface water recharges groundwater again, the biogeochemistry processes repeat as discussed above.