Application of hydrochemistry and stable isotopes (δ34S, δ18O and δ37Cl) to trace natural and anthropogenic influences on the quality of groundwater in the piedmont region, Shijiazhuang, China
2016
Zhou, Jianwei | Zhang, Yanpeng | Zhou, Aiguo | Liu, Cunfu | Cai, Hesheng | Liu, Yunde
Because of their frequent association with man-made products, increasing SO42− and Cl⁻ concentrations are often important indicators of deterioration of groundwater quality. The integrated use of hydrochemistry and multi-isotopic approaches (δ³⁴S, δ¹⁸O and δ³⁷Cl) was applied in Shijiazhuang area, China, to characterize SO42− and Cl⁻ sources; and to evaluate factors, including natural processes and anthropogenic activities, that affect groundwater quality. In the plain area, the SO42− concentrations of the surface water and shallow groundwater (mean 2.42 mmol/L and 2.06 mmol/L, respectively) were generally higher than those of the deep groundwater (mean 0.69 mmol/L). The natural waters in the mountain area (mean 4.36 mmol/L) had higher SO42− contents than those in the plain area (mean 1.73 mmol/L). The shallow groundwater samples collected in the southern part of the plain area had higher Cl⁻ concentrations than other samples. The SO42− in natural waters showed variable δ³⁴S and δ¹⁸O values, ranging from +8.7‰ to +21.7‰ and from +5.9‰ to +11.4‰, respectively. The δ³⁷Cl values fell in a narrow range of −0.22‰ to +0.64‰ with a mean value of +0.14‰. The hydrochemistry of samples is in part controlled by water-rock interaction processes, but also influenced by anthropogenic activities. The variations of δ³⁴S and δ¹⁸O values indicate gypsum, oxidation of inorganic sulfide minerals, and detergents are the primary sources of sulfate in the samples. Bacterial SO42− reduction is an important reaction affecting the SO42− concentrations in the deep groundwater of the plain area. The plot of δ³⁷Cl and 1/Cl⁻ combined with the δ³⁷Cl information of potential Cl⁻ sources suggests that the dissolved Cl⁻ in natural waters is mainly sourced from dissolution of Cl-bearing minerals, import of wastewater, and precipitation. Given the above, the elevated concentration of SO42− and Cl⁻ in the groundwater could be mainly attributed to mining activities in the mountain area and input of wastewater from domestic and industrial activities.
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