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Imaging geochemical heterogeneities using inverse reactive transport modeling: An example relevant for characterizing arsenic mobilization and distribution
Institution:1. Department of Earth System Science, Stanford University, Stanford, CA 94305, USA;2. Department of Civil and Environmental Engineering, Stanford University, Stanford, CA 94305, USA;3. Department of Environmental Engineering, Technical University of Denmark, 2800 Kgs., Lyngby, Denmark;1. Lawrence Berkeley National Laboratory, Climate and Ecosystem Sciences Division, 1 Cyclotron Road, Berkeley, CA 94720, United States;2. Lawrence Berkeley National Laboratory, Energy Geosciences Division, 1 Cyclotron Road, Berkeley, CA 94720, United States;1. Dipartimento di Ingegneria, Roma Tre University, Rome, Italy;2. Department of Civil, Structural and Environmental Engineering, State University of New York at Buffalo, Buffalo, NY, USA;3. Faculty of Engineering, Tel Aviv University, Tel Aviv, Israel;1. Civil Engineering and Engineering Mechanics, Columbia University, New York, NY 10027, United States\n;2. Department of Environmental Science, Barnard College, New York, NY 10027, United States\n;3. Department of Chemistry, Barnard College, New York, NY 10027, United States\n
Abstract:The spatial distribution of reactive minerals in the subsurface is often a primary factor controlling the fate and transport of contaminants in groundwater systems. However, direct measurement and estimation of heterogeneously distributed minerals are often costly and difficult to obtain. While previous studies have shown the utility of using hydrologic measurements combined with inverse modeling techniques for tomography of physical properties including hydraulic conductivity, these methods have seldom been used to image reactive geochemical heterogeneities. In this study, we focus on As-bearing reactive minerals as aquifer contaminants. We use synthetic applications to demonstrate the ability of inverse modeling techniques combined with mechanistic reactive transport models to image reactive mineral lenses in the subsurface and quantify estimation error using indirect, commonly measured groundwater parameters. Specifically, we simulate the mobilization of arsenic via kinetic oxidative dissolution of As-bearing pyrite due to dissolved oxygen in the ambient groundwater, which is an important mechanism for arsenic release in groundwater both under natural conditions and engineering applications such as managed aquifer recharge and recovery operations. The modeling investigation is carried out at various scales and considers different flow-through domains including (i) a 1D lab-scale column (80 cm), (ii) a 2D lab-scale setup (60 cm × 30 cm) and (iii) a 2D field-scale domain (20 m × 4 m). In these setups, synthetic dissolved oxygen data and forward reactive transport simulations are used to image the spatial distribution of As-bearing pyrite using the Principal Component Geostatistical Approach (PCGA) for inverse modeling.
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