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Mercury concentrations and distribution in soil water mine waste leachates and air in and around mercury mines in the Big Bend region Texas USA

机译:美国德克萨斯州大弯地区汞矿及其周围的土壤水矿山垃圾渗滤液和空气中汞的浓度和分布

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摘要

Samples of soil, water, mine waste leachates, soil gas, and air were collected from areas mined for mercury (Hg) and baseline sites in the Big Bend area, Texas, to evaluate potential Hg contamination in the region. Soil samples collected within 300 m of an inactive Hg mine contained elevated Hg concentrations (3.8–11 µg/g), which were considerably higher than Hg in soil collected from baseline sites (0.03–0.05 µg/g) distal (as much as 24 km) from mines. Only three soil samples collected within 300 m of the mine exceeded the probable effect concentration for Hg of 1.06 µg/g, above which harmful effects are likely to be observed in sediment-dwelling organisms. Concentrations of Hg in mine water runoff (7.9–14 ng/L) were generally higher than those found in springs and wells (0.05–3.1 ng/L), baseline streams (1.1–9.7 ng/L), and sources of drinking water (0.63–9.1 ng/L) collected in the Big Bend region. Concentrations of Hg in all water samples collected in this study were considerably below the 2,000 ng/L drinking water Hg guideline and the 770 ng/L guideline recommended by the U.S. Environmental Protection Agency (USEPA) to protect aquatic wildlife from chronic effects of Hg. Concentrations of Hg in water leachates obtained from leaching of mine wastes varied widely from <0.001 to 760 µg of Hg in leachate/g of sample leached, but only one leachate exceeded the USEPA Hg industrial soil screening level of 31 µg/g. Concentrations of Hg in soil gas collected at mined sites (690–82,000 ng/m3) were highly elevated compared to soil gas collected from baseline sites (1.2–77 ng/m3). However, air collected from mined areas at a height of 2 m above the ground surface contained concentrations of Hg (4.9–64 ng/m3) that were considerably lower than Hg in soil gas from the mined areas. Although concentrations of Hg emitted from mine-contaminated soils and mine wastes were elevated, persistent wind in southwest Texas disperses Hg in the air within a few meters of the ground surface.
机译:从得克萨斯州大本德地区汞(Hg)开采地区和基准地点的土壤,水,矿山垃圾渗滤液,土壤气体和空气中收集样品,以评估该地区潜在的汞污染。在不活动的汞矿300 m内收集的土壤样品中的汞浓度升高(3.8-11 µg / g),远高于从基线站点采集的土壤中的Hg(0.03–0.05 µg / g)(多达24个)公里)。在矿井300米范围内收集的三个土壤样品中,汞的可能影响浓度均超过1.06 µg / g,超过此浓度时,在沉积物生物中可能会观察到有害影响。矿泉水径流中的Hg浓度(7.9–14 ng / L)通常高于泉水和水井(0.05–3.1 ng / L),基准流(1.1–9.7ng / L)和饮用水来源中的汞浓度(0.63-9.1ng / L)在大弯地区收集。在这项研究中收集的所有水样中的汞浓度均大大低于美国环境保护署(USEPA)推荐的2,000 ng / L饮用水中Hg准则和770 ng / L准则,以保护水生野生生物免受Hg的慢性影响。从矿山垃圾浸出水中得到的水浸出物中的Hg浓度在每克浸出样品中的<0.001至760 µg Hg中变化很大,但是只有一种浸出液超过了USEPA Hg工业土壤筛选水平31 µg / g。与从基线站点收集的土壤气体(1.2–77ng / m 3 3 )高度升高。 sup>)。但是,从高于地面2 m的采空区收集的空气中所含的Hg浓度(4.9–64ng / m 3 )明显低于采空区土壤气体中的Hg 。尽管从受地雷污染的土壤和矿山废物中释放出的汞浓度有所提高,但得克萨斯州西南部的持续风却将汞散布在离地面几米的空气中。

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