New Geochemical Framework and Geographic Information System Methodologies to Assess Element Occurrence, Persistence, and Mobility in Groundwater and Surface Water

Abstract

This study presents a geochemical framework and geographic information system (GIS) method for assessing the intrinsic potential of surface water and groundwater to mobilize arsenic, molybdenum, selenium, uranium, and vanadium. The method was created using published groundwater and surface water geochemical data from the National Uranium Resource Evaluation database for 2302 groundwater and 915 surface water samples. The method was evaluated using published groundwater geochemical data from the Texas Water Development Board. Geochemical data were analyzed in GIS. Samples were categorized by environmental condition, which was determined by using reduction–oxidation—as indicated by pe—and pH ranges for each sample based on geochemical mobility frameworks developed by Smith (2007) and Perel’man (1986). Reduction–oxidation and pH influence the occurrence, persistence, and mobility of arsenic, molybdenum, selenium, uranium, and vanadium in groundwater and surface water. Reduction–oxidation categories were assigned to water samples using concentrations of redox-active constituents, including dissolved oxygen, iron, manganese, and sulfur. The presence of iron substrates and hydrogen sulfides were considered in relation to mobility mechanisms. Twelve-digit hydrologic unit code (HUC) boundaries were used in GIS as analysis areas to determine the most commonly occurring environmental condition in each HUC. The resulting maps identify the environmental conditions in different areas that can be used to identify where the elements are mobile. This methodology provides a systematic approach to identify areas where elements in groundwater and surface water may occur and persist and may be transferable to other locations.

Keywords

• in situ uranium
• metal mobility
• environmental conditions
• geochemical mechanisms