4.5 Article

Hydrogeochemical characteristics in coastal groundwater mixing zone

Journal

APPLIED GEOCHEMISTRY
Volume 85, Issue -, Pages 49-60

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.apgeochem.2017.09.002

Keywords

Coastal groundwater mixing zone; Seawater-freshwater interface; Cation exchange; Geochemical reactions; Sulfate reduction

Funding

  1. National Natural Science Foundation of China [41372261]
  2. Research Grants Council of Hong Kong [HKU 7028/06P]
  3. Seed Fund for Basic Research [201611159023]

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This study presents the hydrogeochemical analysis in coastal groundwater mixing zone of a sandy aquifer, Ting Kok, Hong Kong. Groundwater samples collected along a sampling transection that covers the salinity transition zone were analyzed for spatial and temporal distribution of major ions (Cl-, SO42- , Na+, K+, Mg2+, and Ca2+) and ancillary parameters such as salinity, pH, temperature, and total alkalinity. The seawater-freshwater interface (SFI) based on different ions, ionic delta of major ions, PHREEQC based saturation index (SI) of minerals are used to systematically investigate geochemical processes such as cation exchange, precipitation/dissolution of minerals, and sulfate reduction under the effect of seasonal hydrologic variation. Compared to Cl--based SFI, the landward movements of cation-based SFI and seaward movement of SO42--based SFI indicate that the coastal aquifer serves as the source of cations and sink of SO42- for groundwater. The SFI is sensitive to seasonal hydrologic variation due to the variation of land-sea hydraulic gradient. The cation exchange and precipitation/dissolution of minerals are dynamic and complex in coastal groundwater mixing zone. The simultaneous enrichment of all cations is found in the aquifer due to external input of a specific cation. The sulfate reduction is responsible for SO42- depletion and also the enrichment of total alkalinity in coastal groundwater mixing zone because gypsum precipitation does not occur according to mineral SI analysis. The cation exchange is very sensitive to the seasonal hydrologic variation while the sulfate reduction is not obviously influenced. (C) 2017 Elsevier Ltd. All rights reserved.

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