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高砷地球化学异常区(法国中央高原)地表水自然砷源的贡献。

Contributions of natural arsenic sources to surface waters on a high grade arsenic-geochemical anomaly (French Massif Central).

机构信息

Université de Limoges, GRESE EA 4330, F.S.T., 123 av. Albert Thomas, 87060 Limoges Cedex, France.

出版信息

Sci Total Environ. 2012 Aug 15;432:257-68. doi: 10.1016/j.scitotenv.2012.05.090. Epub 2012 Jun 27.

Abstract

The subwatershed studied drains a non-exploited area of the St-Yrieix-la-Perche gold mining district (French Massif Central) and it is located on an arsenic (As) geochemical anomaly. In this context, it is important to know the geochemical processes involved in the transfer of As from solid environmental compartments to the aquatic system. The stream showed a temporal variation of dissolved As (As(d)) content from 69.4 μg.L(-1) in the low flow period to 7.5 μg.L(-1) in the high flow period. Upstream, ground- and wetland waters had As(d) concentrations up to 215 and 169 μg.L(-1), respectively. The main representative As sources were determined at the subwatershed scale with in-situ monitoring of major and trace element contents in different waters and single extraction experiments. The As sources to stream water could be regrouped into two components: (i) one As-rich group (mainly in the low flow period) with groundwater, gallery exploration outlet waters and wetland waters, and (ii) one As-poor group (mainly in the high flow period) with rainwaters and soil solutions. In the soil profile, As(d) showed a significant decrease from 52.4 μg.L(-1) in the 0-5 cm superficial soil horizon to 14.4 μg.L(-1) in the 135-165 cm deep soil horizon. This decrease may be related to pedogenic processes and suggests an evolution of As-bearing phase stability through the soil profile. Quantification of As(d) fluxes at the subwatershed scale showed that groundwater was the major input (>80%) of As(d) to surface water. Moreover, natural weathering of the As-rich solid phases showed an impact on the As release, mainly from superficial soil horizons with runoff contributing about 5% to As input in surface water.

摘要

研究的子流域位于圣伊莱尔拉珀什(法国中央高原)金矿开采区的未开发区域,位于砷(As)地球化学异常区。在这种情况下,了解 As 从固体环境成分转移到水生系统的地球化学过程非常重要。溪流的溶解态 As(As(d))含量表现出时间变化,从低流量期的 69.4μg/L 到高流量期的 7.5μg/L。在上游,地下水和湿地水中的 As(d)浓度分别高达 215 和 169μg/L。在子流域尺度上,通过原位监测不同水体中的主要和微量元素含量以及单提取实验,确定了主要的 As 来源。进入溪流的 As 源可分为两个组分:(i)一个富 As 组(主要在低流量期),包括地下水、坑道探测出口水和湿地水,以及 (ii)一个贫 As 组(主要在高流量期),包括雨水和土壤溶液。在土壤剖面中,As(d)从 0-5cm 表层土壤的 52.4μg/L 显著下降到 135-165cm 深处土壤的 14.4μg/L。这种下降可能与成土过程有关,表明 As 赋存相的稳定性在土壤剖面上发生了演变。子流域尺度上的 As(d)通量量化表明,地下水是地表水 As(d)的主要输入源(>80%)。此外,富 As 固相的自然风化对 As 的释放有影响,主要来自表层土壤,径流量约占地表水 As 输入的 5%。

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