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新西兰北地地区矿化岩石上土壤中汞和砷的潜在人为迁移

Potential anthropogenic mobilisation of mercury and arsenic from soils on mineralised rocks, Northland, New Zealand.

作者信息

Craw D

机构信息

Geology Department and Environmental Science Programme, University of Otago, Leith Street, PO Box 56, Dunedin, New Zealand.

出版信息

J Environ Manage. 2005 Feb;74(3):283-92. doi: 10.1016/j.jenvman.2004.10.005. Epub 2004 Dec 15.

Abstract

Eroded roots of hot spring systems in Northland, New Zealand consist of mineralised rocks containing sulfide minerals. Marcasite and cinnabar are the dominant sulfides with subordinate pyrite. Deep weathering and leached soil formation has occurred in a warm temperate to subtropical climate with up to 3 m/year rainfall. Decomposition of the iron sulfides in natural and anthropogenic rock exposures yields acid rock drainage with pH typically between 2 and 4, and locally down to pH 1. Soils and weathered rocks developed on basement greywacke have negligible acid neutralisation capacity. Natural rainforest soils have pH between 4 and 5 on unmineralised greywacke, and pH is as low as 3.5 in soils on mineralised rocks. Roads with aggregate made from mineralised rocks have pH near 3, and quarries from which the rock was extracted can have pH down to 1. Mineralised rocks are enriched in arsenic and mercury, both of which are environmentally available as solid solution impurities in iron sulfides and phosphate minerals. Base metals (Cu, Pb, Zn) are present at low levels in soils, at or below typical basement rock background. Decomposition of the iron sulfides releases the solid solution arsenic and mercury into the acid rock drainage solutions. Phosphate minerals release their impurities only under strongly acid conditions (pH<1). Arsenic and mercury are adsorbed on to iron oxyhydroxides in soils, concentrated in the C horizon, with up to 4000 ppm arsenic and 100 ppm mercury. Waters emanating from acid rock drainage areas have arsenic and mercury below drinking water limits. Leaching experiments and theoretical predictions indicate that both arsenic and mercury are least mobile in acid soils, at pH of c. 3-4. This optimum pH range for fixation of arsenic and mercury on iron oxyhydroxides in soils is similar to natural pH at the field site of this study. However, neutralisation of acid soils developed on mineralised rocks is likely to decrease adsorption and enhance mobility of arsenic and mercury. Hence, development of farmland by clearing forest and adding agricultural lime may mobilise arsenic and mercury from underlying soils on mineralised rocks. In addition, arsenic and mercury release into runoff water will be enhanced where sediment is washed off mineralised road aggregate (pH 3) on to farm land (pH>6). The naturally acid forest soils, or even lower pH of natural acid rock drainage, are the most desirable environmental conditions to restrict dissolution of arsenic and mercury from soils. This approach is only valid where mineralised soils have low base metal concentrations.

摘要

新西兰北地温泉系统的侵蚀根系由含有硫化物矿物的矿化岩石组成。白铁矿和辰砂是主要的硫化物,黄铁矿为次要成分。在年降雨量高达3米的暖温带至亚热带气候条件下,发生了深度风化和淋溶土壤形成过程。天然和人为岩石暴露处的硫化铁分解产生酸性岩排水,其pH值通常在2至4之间,局部低至pH值1。在基底杂砂岩上发育的土壤和风化岩石的酸中和能力可忽略不计。在未矿化的杂砂岩上,天然雨林土壤的pH值在4至5之间,而在矿化岩石上的土壤pH值低至3.5。用矿化岩石制成的集料铺设的道路pH值接近3,开采岩石的采石场pH值可低至1。矿化岩石富含砷和汞,这两种元素在环境中以硫化铁和磷酸盐矿物中的固溶体杂质形式存在。土壤中的贱金属(铜、铅、锌)含量较低,处于或低于典型基底岩石背景值。硫化铁的分解将固溶体中的砷和汞释放到酸性岩排水溶液中。磷酸盐矿物仅在强酸性条件(pH<1)下释放其杂质。砷和汞吸附在土壤中的羟基氧化铁上,集中在C层,砷含量高达4000 ppm,汞含量高达100 ppm。从酸性岩排水区域流出的水体中的砷和汞含量低于饮用水限值。淋溶实验和理论预测表明,砷和汞在pH值约为3 - 4的酸性土壤中迁移性最小。土壤中砷和汞在羟基氧化铁上固定的最佳pH范围与本研究现场的天然pH值相似。然而,矿化岩石上发育的酸性土壤的中和可能会降低吸附作用并增强砷和汞的迁移性。因此,通过砍伐森林和添加农业石灰来开垦农田可能会使矿化岩石下伏土壤中的砷和汞活化。此外,当沉积物从矿化道路集料(pH值3)冲刷到农田(pH值>6)上时,砷和汞向径流水中的释放将会增加。天然酸性森林土壤,甚至天然酸性岩排水更低的pH值,是限制土壤中砷和汞溶解的最理想环境条件。这种方法仅在矿化土壤中贱金属浓度较低时有效。

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