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Free keywords:
combinatorial inverse modelling; thermodynamic equilibrium concept; water–rock interactions; PHREEQC; RedModRphree
Abstract:
The crystalline basement aquifer of the Pra Basin in Ghana is essential to the water supply systems of the region. This region is experiencing the ongoing pollution of major river networks from illegal mining activities. Water management is difficult due to the limited knowledge of hydrochemical controls on the groundwater. This study investigates its evolution based on analyses from a previous groundwater sampling campaign and mineralogical investigation of outcrops. The dominant reactions driving the average groundwater composition were identified by means of a combinatorial inverse modelling approach under the hypothesis of local thermodynamical equilibrium. The weathering of silicate minerals, including albite, anorthite, plagioclase, K-feldspar, and chalcedony, explains the observed median groundwater composition in the transition and discharge zones. Additional site-specific hypotheses were needed to match the observed composition of the main recharge area, including equilibration with carbon dioxide, kaolinite, and hematite in the soil and unsaturated zones, respectively, and the degradation of organic matter controlling the sulfate/sulfide content, thus pointing towards kinetic effects during water–rock interactions in this zone. Even though an averaged water composition was used, the inverse models can “bridge” the knowledge gap on the large basin scale to come up with quite distinct “best” mineral assemblages that explain observed field conditions. This study provides a conceptual framework of the hydrogeochemical evolution for managing groundwater resources in the Pra Basin and presents modelling techniques that can be applied to similar regions with comparable levels of heterogeneity in water chemistry and limited knowledge of aquifer mineralogy. The combinatorial inverse model approach offers enhanced flexibility by systematically generating all plausible combinations of mineral assemblages from a given pool of mineral phases, thereby allowing for a comprehensive exploration of the reactions driving the chemical evolution of the groundwater.
