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Ion exchange and trace element surface complexation reactions associated with applied recharge of low-TDS water in the San Joaquin Valley,California
Authors:Walt W McNab Jr  Michael J Singleton  Jean E Moran  Bradley K Esser
Institution:1. Environmental Restoration Department, Lawrence Livermore National Laboratory, P.O. Box 808, L-530, Livermore, CA 94551, USA;2. Chemical Biology and Nuclear Science Division, Lawrence Livermore National Laboratory, USA;3. Department of Earth and Environmental Science, California State University, East Bay, Hayward, CA, USA
Abstract:Stable isotope data, a dissolved gas tracer study, groundwater age dating, and geochemical modeling were used to identify and characterize the effects of introducing low-TDS recharge water in a shallow aerobic aquifer affected by a managed aquifer recharge project in California’s San Joaquin Valley. The data all consistently point to a substantial degree of mixing of recharge water from surface ponds with ambient groundwater in a number of nearby wells screened at depths above 60 m below ground surface. Groundwater age data indicate that the wells near the recharge ponds sample recently recharged water, as delineated by stable O and C isotope data as well as total dissolved solids, in addition to much older groundwater in various mixing proportions. Where the recharge water signature is present, the specific geochemical interactions between the recharge water and the aquifer material appear to include ion exchange reactions (comparative enrichment of affected groundwater with Na and K at the expense of Ca and Mg) and the desorption of oxyanion-forming trace elements (As, V, and Mo), possibly in response to the elevated pH of the recharge water.
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