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地下水高钼的自然来源与人为来源:来自美国威斯康星州东南部的地球化学污染证据。

Naturally Occurring versus Anthropogenic Sources of Elevated Molybdenum in Groundwater: Evidence for Geogenic Contamination from Southeast Wisconsin, United States.

机构信息

Division of Earth and Ocean Sciences, Nicholas School of the Environment, Duke University , Durham, North Carolina 27708, United States.

Divisions of Solid Earth Dynamics and Water, Climate and the Environment, School of Earth Sciences, The Ohio State University , Columbus, Ohio 43210, United States.

出版信息

Environ Sci Technol. 2017 Nov 7;51(21):12190-12199. doi: 10.1021/acs.est.7b03716. Epub 2017 Oct 19.

Abstract

Molybdenum (Mo) is an essential trace nutrient but has negative health effects at high concentrations. Groundwater typically has low Mo (<2 μg/L), and elevated levels are associated with anthropogenic contamination, although geogenic sources have also been reported. Coal combustion residues (CCRs) are enriched in Mo, and thus present a potential anthropogenic contamination source. Here, we use diagnostic geochemical tracers combined with groundwater residence time indicators to investigate the sources of Mo in drinking-water wells from shallow aquifers in a region of widespread CCR disposal in southeastern Wisconsin. Samples from drinking-water wells were collected in areas near and away from known CCR disposal sites, and analyzed for Mo and inorganic geochemistry indicators, including boron and strontium isotope ratios, along with groundwater tritium-helium and radiogenic He in-growth age-dating techniques. Mo concentrations ranged from <1 to 149 μg/L. Concentrations exceeding the U.S. Environmental Protection Agency health advisory of 40 μg/L were found in deeper, older groundwater (mean residence time >300 y). The B (δB = 22.9 ± 3.5‰) and Sr (Sr/Sr = 0.70923 ± 0.00024) isotope ratios were not consistent with the expected isotope fingerprints of CCRs, but rather mimic the compositions of local lithologies. The isotope signatures combined with mean groundwater residence times of more than 300 years for groundwater with high Mo concentrations support a geogenic source of Mo to the groundwater, rather than CCR-induced contamination. This study demonstrates the utility of a multi-isotope approach to distinguish between fossil fuel-related and natural sources of groundwater contamination.

摘要

钼(Mo)是一种必需的痕量营养元素,但在高浓度下会对健康产生负面影响。地下水通常钼含量较低(<2μg/L),并且高浓度与人为污染有关,尽管也有报道称存在地球成因来源。煤燃烧残留物(CCR)富含钼,因此是潜在的人为污染来源。在这里,我们使用诊断地球化学示踪剂结合地下水滞留时间指标,调查了威斯康星州东南部广泛存在 CCR 处置区浅层含水层中饮用水井中 Mo 的来源。在靠近和远离已知 CCR 处置地点的地区收集了饮用水井的样本,并分析了 Mo 和无机地球化学指标,包括硼和锶同位素比值,以及地下水氚-氦和放射性氦的内生长年龄测定技术。Mo 浓度范围从<1 到 149μg/L。在更深、更老的地下水(平均滞留时间>300 年)中发现了超过美国环境保护署健康咨询值 40μg/L 的浓度。B(δB=22.9±3.5‰)和 Sr(Sr/Sr=0.70923±0.00024)同位素比值与 CCR 预期的同位素指纹特征不一致,而是类似于当地岩性的组成。同位素特征与 Mo 浓度较高的地下水超过 300 年的平均地下水滞留时间相结合,支持 Mo 地下水的地球成因来源,而不是 CCR 引起的污染。本研究表明,多同位素方法可用于区分地下水污染的化石燃料相关和自然来源。

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