STABLE ISOTOPE CHARACTERIZATION OF THE IMPACTS OF ARTIFICIAL GROUND WATER RECHARGE1

Abstract

ABSTRACT: Stable isotopes of deuterium and oxygen‐18 of surface and ground water, together with anion concentrations and hydraulic gradients, were used to interpret mixing and flow in ground water impacted by artificial recharge. The surface water fraction (SWF), the percentage of surface water in the aquifer impacted via recharge, was estimated at different locations and depths using measured deuterium/hydrogen (DIH) ratios during the 1992, 1993, and 1994 recharge seasons. Recharged surface water completely displaced the ground water beneath the recharge basins from the regional water table at 7.60 m to 12.16 m below the land surface. Mixing occurred beneath the recharge structures in the lower portions of the aquifer (>12.16 m). Approximately 12 m down‐gradient from the recharge basin, the deeper zone (19.15 m depth) of the primary aquifer was displaced completely by recharged surface water within 193, 45, and 55 days in 1992, 1993, and 1994, respectively. At the end of the third recharge season, recharged surface water represented ∼50 percent of the water in the deeper zone of the primary aquifer ∼1000 m downgradient from the recharge basin. A classic asymmetrical distribution of recharged surface water resulted from the recharge induced horizontal and vertical hydraulic gradients. The distribution and breakthrough times of recharged surface water obtained with stable isotopes concurred with those of major anions and bromide in a tracer test conducted during the 1995 recharge season. This stable isotope procedure effectively quantified mixing between surface and ground water.