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多种机制导致中国北方两个相邻地区地下水中氟的富集。

Diverse mechanisms drive fluoride enrichment in groundwater in two neighboring sites in northern China.

机构信息

School of Environmental Studies, China University of Geosciences, Wuhan 430074, China.

School of Environmental Studies, China University of Geosciences, Wuhan 430074, China.

出版信息

Environ Pollut. 2018 Jun;237:430-441. doi: 10.1016/j.envpol.2018.02.072. Epub 2018 Mar 15.

Abstract

Excessive amounts of fluoride in drinking groundwater are harmful to human health, but the mechanisms responsible for fluoride enrichment in groundwater are not fully understood. Samples from two neighboring areas with endemic fluorosis were collected to test the hypothesis that there are distinctly different mechanisms responsible for the enrichment of fluoride in these groundwater. Hydrochemistry, stable isotopes and geochemical simulation were conducted together to investigate the fluoride spatial distribution and the diversity of responsible mechanisms. Our results showed that the spatial distributions of fluoride are different: I) high [F] in fresh shallow groundwater (SG) and II) medium [F] in fresh to brackish deep groundwater (DG) in the Qiji area; and III) medium [F] in brackish shallow groundwater (SG) and IV) low [F] in fresh deep groundwater (DG) in the Yanhu area. We also found that the fluoride concentration in groundwater is primarily controlled by the dissolution equilibrium of fluorite, as suggested by the correlation between [F] and [Ca]. However, there are other significant mechanisms: 1) for SG, fluoride-bearing minerals (such as fluorite) dissolution, along with moderate evaporation, cation exchange and the more alkaline conditions are the driving factors; 2) for SG, the contributing factors are strong evaporation, the salt effect, dissolution of evaporites, gypsum and dolomite, bicarbonate-fluoride competition and anthropogenic activity; 3) for DG, cation exchange, alkaline conditions and competitive adsorption are major factors; and 4) dolomite dissolution promotes the [F] increase in DG. Our findings suggest that the hydrogeochemical conditions play key roles in the enrichment of fluoride and that caution should be taken in the future when evaluating fluoride occurrence in groundwater, even in nearby areas.

摘要

饮用地下水中超量的氟化物对人体健康有害,但导致地下水富氟的机制尚未完全了解。本研究采集了两个地方性氟中毒病区的地下水样本,以验证地下水氟富集存在截然不同的机制的假设。通过水化学、稳定同位素和地球化学模拟,研究了氟的空间分布和不同的机制。研究结果表明,氟的空间分布不同:i)奇集地区浅层淡水(SG)中氟含量高[F];ii)深层淡水(DG)中氟含量为中等至咸水[F];iii)沿湖地区浅层咸水(SG)中氟含量中等[F];iv)深层淡水(DG)中氟含量低[F]。此外,研究还发现,氟在地下水中的浓度主要受萤石溶解平衡的控制,这可以通过氟和钙之间的相关性来证明。然而,还存在其他重要的机制:i)对于 SG,氟化物矿物(如萤石)的溶解,以及适度的蒸发、阳离子交换和更碱性的条件是驱动因素;ii)对于 SG,强蒸发、盐效应、蒸发盐、石膏和白云石的溶解、重碳酸盐-氟竞争和人为活动是主要因素;iii)对于 DG,阳离子交换、碱性条件和竞争吸附是主要因素;iv)白云石的溶解促进了 DG 中氟的增加。本研究结果表明,水地球化学条件在氟的富集中起着关键作用,即使在附近地区,未来在评估地下水氟化物的存在时也应谨慎。

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