COUPLED GROUNDWATER AND VOLATILE ORGANIC COMPOUND FLUXES THROUGH A STREAMBED CONTRIBUTE TO OFF-SITE MIGRATION OF CONTAMINANTS IN A COASTAL PLAIN STREAM, NORTH CAROLINA
The groundwater analyses indicate thirteen VOCs discharge to HSC: tetrachloroethene (PCE), trichloroethene (TCE), 1,1-dichloroethene (DCE), cis-1,2-dichloroethene (cDCE), trans-1,2-dischloroethene (tDCE), vinyl chloride (VC), benzene (BZ), 1,3-butadiene (BT), 1,1,2,2-tetrachloroethane (PCA), 1,1-dichloroethane (1,1-DCA), 1,2-dichloroethane (1,2-DCA), 1,2,3-trichlorpropane (TCP), and 1,2-dichloropropane (DCP). Interpolated, contoured maps of fvoc reveal large spatial variability in the 52-m reach. Chlorinated ethenes and DCP primarily discharge on the right side of the stream channel, in the upper third of the reach near a dry cleaner. Chlorinated ethanes, BZ, BT, and TCP primarily discharge on the left hand side of the stream channel, in the middle third of the reach. The spatial variability suggests at least 2 plumes with different chemical sources. The highest fvoc was that for cDCE, at 9.98 mg m-2 d-1, followed by BZ (6.56 mg m-2 d-1) and VC (1.81 mg m-2 d-1). Other fvoc values were less than 1 mg m-2 d-1. Higher fvoc values generally occurred in areas of higher v. The annual mass losses of cDCE, BZ, and VC from the aquifer to the stream reach were estimated to be 1.11, 0.73, and 0.20 kg yr-1, respectively. Annual mass losses for other VOCs were less than 0.02 kg yr-1. The spatial variation of VOC fluxes gives quantitative insight into the impact of multiple plumes discharging to a single urban stream.