摘要

To further define the hydro-geochemical circulation in estuary from a mountainous island, over 50 river water samples were collected in three sampling schemes from the Gaoping River Estuary (GRE), the largest river catchment in southwestern Taiwan and were analyzed for major/trace elements, uranium (U) and strontium (Sr) isotopic compositions using multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS). Dissolved U and Sr concentrations (0.46-13.8 nM and 2.27-86.2 mu M), as well as U activity ratio (denoted as (U-234/U-238)) and Sr-87/Sr-88 (1.145-2.427 and 0.709155-0.712918), vary significantly and show strong seasonal variability. Three characteristic source waters were identified in the study region, seawater (SW), river water (RW), and groundwater (GW or evolved RW). SW has the highest U and Sr concentrations among the three end-members with low and constant (U-234/U-238) and Sr-87/Sr-88. In contrast, RW shows the lowest U and an intermediate Sr concentration, but with medium (U-234/U-238) and the most radiogenic Sr-87/Sr-86. GW has the medium U and lowest Sr content with rather radiogenic (U-234/U-238) and Sr-87/Sr-88, possibly evolved from RW. The GW is most clearly identified in the vertical profile of the near estuary stations. These high (U-234/U-238) values in RW and GW reflect the outcome of intense weathering in the upper catchment, efficient leaching of at-recoil products in soils. Dissolved Sr and Sr-82/Sr-88 data confirm similar U mixing scenarios, but the index is more sensitive to water source variations. Estimated fluxes of submarine groundwater discharge (SGD) in the GRE reach a maximum value of 456-2107 x 10(11) L yr(-1), implying important contribution to the chemical budget in coastal regions. This study reveals that U and Sr isotopes are useful tracers for monitoring SGD in estuaries.

  • 出版日期2013-12-20

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