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巴基斯坦信德省拉尔卡纳地区地下水砷富集是回灌灌溉水垂直混合造成的。

Vertical mixing with return irrigation water the cause of arsenic enrichment in groundwater of district Larkana Sindh, Pakistan.

机构信息

Hydro Geochemistry Laboratory, Department of Environmental Sciences, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, PO, 45320, Pakistan; State Key Laboratory of Environmental Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences, Guiyang, 550081, China; University of Chinese Academy of Sciences, Beijing, 100049, China.

Hydro Geochemistry Laboratory, Department of Environmental Sciences, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, PO, 45320, Pakistan.

出版信息

Environ Pollut. 2019 Feb;245:77-88. doi: 10.1016/j.envpol.2018.10.103. Epub 2018 Oct 29.

Abstract

Stable isotopes ratios (‰) of Hydrogen (δH) and Oxygen (δ⁸O) were used to trace the groundwater recharge mechanism and geochemistry of arsenic (As) contamination in groundwater from four selected sites (Larkana, Naudero, Ghari Khuda Buksh and Dokri) of Larkana district. The stable isotope values of δH and δ⁸O range from 70.78‰ to -56.01‰ and from -10.92‰ to -7.35‰, relative to Vienna Standard for Mean Ocean Water (VSMOW) respectively, in all groundwater samples, thus indicating the recharge source of groundwater from high-salinity older water. The concentrations of As in all groundwater samples were ranged from 2 μg/L to 318 μg/L, with 67% of samples exhibited As levels exceeding than that of World Health Organization (WHO) permissible limit 10 μg/L and 42% of samples expressed the As level exceeding than that of the National Environmental Quality Standard (NEQS) 50 μg/L. The leaching and vertical mixing with return irrigation water are probably the main processes controlling the enrichment of As in groundwater of Larkana, Naudero, Ghari Khuda Buksh and Dokri. The weathering of minerals mostly controlled the overall groundwater chemistry; rock-water interactions and silicate weathering generated yielded solutions that were saturated in calcite and dolomite in two areas while halite dissolution is prominent with high As area.

摘要

稳定同位素比值(‰)的氢(δH)和氧(δ⁸O)被用来追踪地下水补给机制和砷(As)污染的地球化学在拉卡纳区四个选定地点(拉卡纳、瑙德罗、Ghari Khuda Buksh 和 Dokri)的地下水中。所有地下水样本的 δH 和 δ⁸O 稳定同位素值范围分别为 70.78‰至-56.01‰和-10.92‰至-7.35‰,相对于维也纳标准平均海水(VSMOW),这表明地下水的补给源来自高盐度的老水。所有地下水样本中的 As 浓度范围为 2μg/L 至 318μg/L,其中 67%的样本显示 As 水平超过世界卫生组织(WHO)允许限值 10μg/L,42%的样本显示 As 水平超过国家环境质量标准(NEQS)50μg/L。淋滤和与回灌水的垂直混合可能是控制拉卡纳、瑙德罗、Ghari Khuda Buksh 和 Dokri 地下水砷富集的主要过程。矿物的风化主要控制着地下水的整体化学性质;岩石-水相互作用和硅酸盐风化产生的溶液在两个地区均处于方解石和白云石的饱和状态,而在高砷地区,氯化钠的溶解则较为突出。

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