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Geochemical signatures and isotopic systematics constraining dynamics of fluoride contamination in groundwater across Jamui district, Indo-Gangetic alluvial plains, India

机译:印度印度恒河冲积平原Jamii地区地下水中氟化物污染动态的地球化学特征和同位素系统学

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A data set of 76 water samples are obtained from surface and sub-surface water bodies to investigate chemical parameters and stable isotopic signatures in order to drive factors leading to fluoride (F-) contamination in groundwater of parts of Jamui district, India. Hydrochemical facies reveals that F- concentration is lower in Ca2+-HCO3- facies representative of recharge area, while discharge area has a tendency towards Na+-HCO3- facies with elevated F- concentration. The ionic ratios Na+/Ca2+1, Na+/(Ca2++Mg2+)/FICO3(-)1, Na++K+ = 0.5TZ(+) and Ca2++Mg2+ = TZ(+) witness silicate weathering by water-rock interaction coupled with ion exchange and prolonged residence time, are the principle factors for fluoride contamination (3.6 mg/L to 5.8 mg/L) in 67% of deeper bore wells. Geochemical modelling testifies excess of alkalinity due to the dominance of bicarbonate ion leading to calcite precipitation and dissolution of fluoride in solution contributing to fluoride contamination. The chemometric analysis reveals that the water chemistry of the study area is controlled by both anthropogenic and natural sources, and enrichment of fluoride in groundwater is possibly from geogenic source (fractured granite gneiss). The stable isotope plot shows that most of the samples fall along local meteoric water line indicating that the groundwater is originated from local precipitation with a possibility of evaporative enrichment. Groundwater enriched in 8180 is positively correlated with F- suggesting evaporation and longer residence time of water. Spatially elevated F- prevails in the eastern bank of Kiul River and along the groundwater flow direction, which is attributed to control of dynamics of hydrogeological conditions. (C) 2018 Elsevier Ltd. All rights reserved.
机译:从地表和地下水体获得了76个水样本的数据集,以研究化学参数和稳定的同位素特征,以驱动印度Jamui区部分地区地下水中导致氟化物(F-)污染的因素。水化学相表明,在代表补给区的Ca2 + -HCO3-相中F-浓度较低,而放电区则随着F-浓度的升高而趋向于Na + -HCO3-相。离子比Na + / Ca2 +> 1,Na + /(Ca2 ++ Mg2 +)/ FICO3(-)<1,Na ++ K + = 0.5TZ(+)和Ca2 ++ Mg2 + = TZ(+)见证了硅酸盐在水中的风化作用岩石相互作用与离子交换和延长的停留时间是在67%的较深井眼中氟化物污染(3.6 mg / L至5.8 mg / L)的主要因素。地球化学模型证明,由于碳酸氢根离子占主导地位而导致碱度过高,从而导致方解石沉淀和溶液中氟化物的溶解,导致氟化物污染。化学计量分析表明,研究区的水化学受人为和自然资源的控制,地下水中氟化物的富集可能来自地源(花岗岩片麻岩)。稳定的同位素图表明,大多数样品都沿着局部的流水线下降,表明地下水源自局部降水,并可能蒸发富集。富含8180的地下水与F-正相关,表明水分蒸发和更长的停留时间。空间升高的F-普遍存在于基尔河东岸和沿地下水流向,这归因于对水文地质条件动态的控制。 (C)2018 Elsevier Ltd.保留所有权利。

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