4.7 Article

Mercury pollution in the coastal Urmia aquifer in northwestern Iran: potential sources, mobility, and toxicity

Journal

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
Volume 28, Issue 14, Pages 17546-17562

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11356-020-11865-y

Keywords

Groundwater; Hydrogeochemistry; Mercury; Source; Mobility; Coastal aquifer

Funding

  1. National Natural Science Foundation of China [41761144059, 42072286]
  2. Fundamental Research Funds for the Central Universities of CHD [300102299301]
  3. Fok Ying Tong Education Foundation [161098]
  4. Ten Thousand Talent Program [W03070125]

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The study investigated the concentration of total dissolved mercury (Hg-T) in groundwater in the coastal parts of Urmia aquifer in Iran, identifying geological weathering as a main source of mercury. One sample exceeded the maximum contaminant level recommended by WHO. The distribution of water samples on the Piper diagram indicated Ca-Mg-HCO3 facies predominance, while the positive correlation of Hg-T with various elements suggested geological formations as a significant source of mercury. Water samples in Eh-pH regions showed potential microbial activity related to mercury methylation and mineralization, indicating sulfate reduction processes and limited anaerobic conditions. The study also found some Hg-bearing species in nonequilibrium geochemical conditions and speculated on the role of Fe-bearing minerals in reducing Hg(II) to Hg(0).
The concentration of total dissolved mercury (Hg-T) in surface and groundwater resources in the coastal parts of Urmia aquifer (NW of Iran) was investigated to identify the possible sources and sinks of mercury and the geochemical mechanisms controlling its mobilization. The distribution of water samples on the Piper diagram demonstrates that most samples have the Ca-Mg-HCO3 facies. From 62 water samples collected in this area, one sample contained Hg-T concentrations exceeding the maximum contaminant level recommended by the WHO (6 mu g/L). The principal component analysis (PCA) produced five principal components. The positive moderate correlation of Hg-T with EC, Cl, K, Mg, and Na indicated that the weathering of geological formations was one of the main sources of mercury in groundwater samples. Position of water samples in Eh-pH regions where microorganisms involved in mercury methylation and mineralization were potentially active demonstrated that the aquifer had undergone sulfate reduction and had reached the final stage of the terminal electron accepting process (TEAP) sequence in the methane production processes which are limited to only 37% of the water samples that have anaerobic conditions. Some Hg-bearing species are in nonequilibrium geochemical conditions. The supersaturation of water samples with magnetite and goethite indicated that these Fe-bearing minerals could act as the strong reducing agents for the reduction of Hg(II) to Hg(0).

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