IMMOBILIZATION OF GROUNDWATER ARSENIC IN RIVER BANK SEDIMENT FROM THE GANGES-BRAHMAPUTRA-MEGHNA RIVER DELTA
In January 2006, we collected 33 sediment cores down to 7 m depth with 102 sediment and 20 pore water samples, 18 shallow well water and 6 river water samples from 18 sites along Meghna and Brahmaputra Rivers. The first area is located at ~ 23.4 N on the Meghna River where most existing shallow wells (< 25 m) contained >50 ug/L As. The second area is located at ~ 24.6 N on the Brahmaputra River where nearly all shallow wells contained < 10 ug/L As. The concentrations of 1.2M HCl extractable As, PO4, Fe in sediment samples were measured in the field by colorimetry and re-analyzed in the laboratory by high resolution inductively plasma mass spectrometry (HR ICP-MS). Water samples were also analyzed by HR ICP-MS for major cations, As, Fe, Mn, S and P. The speciation of As sorbed on sediment was determined by voltammetry after an anaerobic extraction by 1 M phosphate with 0.1 M L-ascorbic acid.
Several sediment cores from the Meghna River site displayed high As much greater than the crustal value of sediment of ~ 10 mg/kg, with the maximum of HCl-leachable As detected as 709 mg/kg at 0.3 m. Most of the P-extractable As were in the form of arsenite. None of the 5 cores from the Brahmaputra site had elevated sedimentary As. Concentrations of Fe, As, P displayed a stronger decreasing trend from existing shallow wells to river bank sediment pore water, and finally to the river water than that of the major cations such as Ca, Mg, K and Na. Our results illustrate that elevated sediment As resulted from groundwater-river water interaction in a natural reactive barrier most likely consisted of Fe minerals, preventing As from leaving the system. Recycling of this As to the Ganges-Brahmaputra-Meghna Delta (GBMD) aquifer provides a potential source of As.