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Natural spatial and temporal variations in groundwater chemistry in fractured,sedimentary rocks: scale and implications for solute transport
Affiliation:1. Environmental Geophysics Associates, Austin, TX, United States;2. City of Austin Watershed Protection Department, Austin, TX, United States;1. Technische Universität Clausthal, Institut für Geophysik, 38678 Clausthal-Zellerfeld, Germany;2. Department of Earth & Environmental Sciences, Rutgers University-Newark, Newark, NJ 07102, United States
Abstract:Natural tracers (major ions, δ18O, and O2) were monitored to evaluate groundwater flow and transport to a depth of 20 m below the surface in fractured sedimentary (primarily shale and limestone) rocks. Large temporal variations in these tracers were noted in the soil zone and the saprolite, and are driven primarily by individual storm events. During nonstorm periods, an upward flow brings water with high TDS, constant δ18O, and low dissolved O2 to the water table. During storm events, low TDS, variable δ18O, and high dissolved O2 water recharges through the unsaturated zone. These oscillating signals are rapidly transmitted along fracture pathways in the saprolite, with changes occurring on spatial scales of several meters and on a time scale of hours. The variations decreased markedly below the boundary between the saprolite and less weathered bedrock. Variations in the bedrock units occurred on time scales of days and spatial scales of at least 20 m. The oscillations of chemical conditions in the shallow groundwater are hypothesized to have significant implications for solute transport. Solutes and colloids that adsorb onto aquifer solids can be released into solution by decreases in ionic strength and pH. The decreases in ionic strength also cause thermodynamic undersaturation of the groundwater with respect to some mineral species and may result in mineral dissolution. Redox conditions are also changing and may result in mineral dissolution/precipitation. The net result of these chemical variations is episodic transport of a wide range of dissolved solutes or suspended particles, a phenomenon rarely considered in contaminant transport studies.
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