A 24 h investigation of the hydrogeochemistry of baseflow and stormwater in an urban area impacted by mining: Butte,Montana     

Christopher H. Gammons  Christopher L. Shope  Terence E. Duaime 《水文研究》2005,19(14):2737-2753

Changes in water quality during a storm event were continuously monitored over a 24 h period at a single location along an urban stormwater drain in Butte, Montana. The Butte Metro Storm Drain (MSD) collects groundwater baseflow and stormwater draining Butte Hill, a densely populated site that has been severely impacted by 130 years of mining, milling, and smelting of copper‐rich, polymetallic mineral deposits. On the afternoon of 26 June 2002, a heavy thunderstorm caused streamflow in the MSD to increase 100‐fold, from 0·2 ft³ s⁻¹ to more than 20 ft³ s⁻¹. Hourly discharge and water quality data were collected before, during, and following the storm. The most significant finding was that the calculated loads (grams per hour) of both dissolved and particulate copper passing down the MSD increased more than 100‐fold in the first hour following the storm, and remained elevated over baseline conditions for the remainder of the study period. Other metals, such as zinc, cadmium, and manganese, showed a decrease in load from pre‐storm to post‐storm conditions. In addition to the large flush of copper, loads of soluble phosphorus increased during the storm, whereas dissolved oxygen dropped to low levels (<2 mg l⁻¹). These results show that infrequent storm events in Butte have the potential to generate large volumes of runoff that exceed Montana water quality standards for acute exposure of aquatic life to copper, as well as depressed levels of dissolved oxygen. This study has important implications to ongoing reclamation activities in the upper Clark Fork Superfund site, particularly with respect to management of storm flow, and may be applicable to other watersheds impacted by mining activities. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

湖南金鸡岭花岗岩和伟晶岩中黑云母矿物化学及其对成岩成矿的启示     

汪志杰  闫峻  徐琳玉  陶克勤  李全忠 《地质论评》2023,69(5):1795-1816

湖南晚侏罗世金鸡岭花岗岩体是南岭地区典型W—Sn成矿岩体之一,内部发育黑云母花岗质伟晶岩团块和文象花岗质条带状伟晶岩脉。金鸡岭花岗岩和黑云花岗伟晶岩中的黑云母具有相似的地球化学特征,均表现出高的FeO、TiO₂、Al₂O₃含量和低的MgO、CaO、Na₂O、MnO含量,以及富集成矿元素Nb、Ta、W、Sn,亏损Sr、Ce、Eu等微量元素特征,从花岗岩体到黑云花岗伟晶岩,岩浆的形成温度和氧逸度降低,云母中Al₂O₃、Li₂O^*含量升高,TiO₂、MgO含量降低,黑云母由铁叶云母演变为黑鳞云母。结合前人资料,金鸡岭花岗岩与黑云花岗伟晶岩均源于元古宙地壳的深熔作用,伟晶岩为花岗岩浆在晚期分异演化的产物,形成于岩浆—热液转化阶段。伟晶岩阶段是稀有金属元素显著富集,乃至进一步成矿的重要阶段。  相似文献   

黔北上二叠统底部发现REY、Nb、Zr和Li等关键金属异常富集层     

谯文浪  杨瑞东  季国松  龙建喜  陈登 《地质论评》2023,69(6):2111-2114

在黔北上二叠统底部铁铝质黏土岩、下部煤层及其顶底板炭质黏土岩中发现其富集稀土、铌、锆和锂等关键金属元素,其中铁铝质黏土岩REY、Nb、Zr和Li平均含量分别为807×10^-6、143×10^-6、1107×10^-6、375×10^-6,下部煤层及其顶底板炭质黏土岩中REY、Nb、Zr和Li平均含量为分别为555×10^-6、104×10^-6、786×10^-6、116×10^-6。显示出该区域该层位具有关键金属矿床良好的找矿前景。  相似文献   

基于可见—近红外反射光谱的典型农田重金属污染风险分类研究     

李全坤  赵万伏  文宇博  郭超  刘连文  季峻峰 《高校地质学报》2022,28(6):799-813

对于人为因素或自然因素造成的农田土壤重金属元素污染,需要进行大面积的土壤环境质量调查和分类管控,然而传统的采样测试方法存在工作量大、代价高等问题。可见—近红外（Vis-NIR）反射光谱是一种快速低成本获取土壤理化信息的手段。为研究Vis-NIR反射光谱预测模型划分土壤重金属污染风险类别的能力,文章以典型人为污染地区（浙江温岭）和典型地质高背景地区（广西横县）的390份农田土壤为样本,测定8种重金属元素（As、Cd、Cr、Cu、Hg、Ni、Pb和Zn）的含量和pH值,并测定土壤Vis-NIR光谱。使用偏最小二乘（PLS）和支持向量机（SVM）算法建立回归模型,对土壤重金属含量和pH值进行预测,并基于预测值进行土壤重金属污染风险分类。结果显示,温岭土壤主要污染元素Cd和Cu的光谱模型回归预测偏差（RPD）分别为1.23和1.19,预测机制与有机质有关。横县土壤主要污染元素As和Cd的RPD分别为1.98和1.93,预测机制与铁氧化物和粘土矿物有关。地质高背景土壤重金属与铁氧化物的正相关性普遍较强,使得光谱模型对重金属含量预测准确度较高。温岭和横县土壤pH值的光谱模型RPD分别为1.76和1.68。土壤重金属污染风险光谱分类的总体 准确度分别为75.0%~100%（温岭）和80.0%~100％（横县）。将Vis-NIR光谱与遥感技术相结合,对农田土壤重金属污染风险进行快速分类总体是可行的。  相似文献   

内蒙古新巴尔虎右旗土壤重金属生态风险与来源分析          下载免费PDF全文

杨玲  田磊  白光宇  裴圣良  张德强 《中国地质》2022,49(6):1970-1983

【研究目的】新巴尔虎右旗地处呼伦贝尔草原深处,矿业活动频繁。了解该地区土壤中重金属来源以及生态风险是评估区域环境影响前提。【研究方法】本文系统采集了矿石、基岩及土壤样品共221件,测试并分析了Cd、Cr、As、Hg、Ni、Pb、Zn等7种重金属元素的含量。利用地积累指数法和潜在生态风险指数法评价了重金属的污染程度和生态风险,并综合运用相关分析、主成分分析法判断了土壤重金属的来源。【研究结果】研究表明,新巴尔虎右旗土壤重金属污染以轻度为主,Cd、Ni、As、Cr、Pb元素均存在一定程度的污染,污染区域集中于甲查矿区、准乌兰诺尔、呼伦湖西北岸以及克鲁伦河中游。Cr、Ni、Hg主要受人类活动影响;Cd、Zn、Pb受到自然因素与人类活动共同影响,As主要受自然因素影响。【结论】总体来看,本区生态风险整体较低,以Cd对生态风险的贡献最为突出,在本区土壤质量监测中应受到重视。  相似文献   

黔西北地区土壤重金属地球化学背景及管理目标值     

孟伟  莫春虎  刘应忠 《物探与化探》2022,(1):250-257

基于贵州省毕节地区1∶25万土地质量地球化学调查的1 308件深层土壤样品重金属含量数据,研究了土壤重金属含量分布及其地球化学背景特征,与全国土壤比较,黔西北土壤重金属地球化学背景值显著高于全国土壤元素背景值,但是,与我国西南地区土壤元素背景值接近。黔西北地区土壤重金属含量与地质背景关系密切,不同地质单元区土壤重金属含量存在显著差异,石炭系地层发育的土壤呈Pb、Zn地球化学高背景,二叠系中统风化形成的土壤呈Cd、Hg地球化学高背景,黔西北地区不仅存在土法炼锌造成的土壤重金属污染,土壤重金属地球化学高背景也是影响土壤重金属富集的重要因素。统计表明,黔西北地区二叠系中统风化土壤Cd管理目标值高于我国农用地土壤Cd风险管制值(2.0×10^-6),认为在确定黔西北地区土壤重金属管理目标时,应充分考虑不同地质单元区土壤重金属地球化学背景值差异及其生态环境效应的影响。  相似文献   

内蒙古林西县北三段银铅多金属矿床碳、氧、硫、铅同位素特征及成矿物质来源     

吕向光 《地质与勘探》2015,51(5):898-906

本文对内蒙古林西县北三段银铅多金属矿床矿体的碳、氧、硫、铅同位素进行了测定,并对其成矿物质来源及演化进行了探讨。矿区样品的δ34S‰变化范围为-0.24‰~2.37‰,平均值为1.29‰,初步认为矿石中的硫主要来源于深部岩浆,并有少量生物还原硫的加入。样品的δ13CPDB变化范围为-4.57‰~-7.33‰,平均值为-5.96‰,δ18O为-3.4‰~-4.8‰,平均值为-4.06‰;δ13CPDB-δ18OSMOW关系表明,矿体中的碳可能主要由基性-超基性岩浆提供,并有部分来源于地层,且受大气水影响明显。铅同位素表明北三段矿床的成矿物质可能由造山带物质和地幔物质两部分提供。  相似文献   

基于生物可利用性与宽浓度范围的Hakanson潜在生态风险指数法的创建——以小秦岭金矿区农田土壤为例   总被引：2，自引：0，他引：2  

卢聪  李涛  付义临  徐友宁  张江华  吴耀国 《地质通报》2015,34(11):2054-2060

Hakanson潜在生态风险指数法是土壤重金属潜在生态风险评价的一种常用方法,研究与实践证明其有效性的同时,也发现了其不足之处:忽略了土壤重金属不同形态之间潜在生态风险的差异,且只重视重金属含量高于参考值时的生态风险,而对低于参考值时的情况没有给予考虑,以致特定情况下的评价结果不能很好地反映实际生态风险,因而有必要创建适用性更广的Hakanson潜在生态风险指数法。为此,基于全过程控制优化的思想,引入了生物可利用性毒性系数,并将修正浓度与参考值差值引入计算公式,创建了基于生物可利用性与宽浓度范围的Hakanson潜在生态风险指数法,实现了对重金属不同形态风险贡献的差异及重金属浓度低于参考值情况下潜在生态风险的准确把握。以小秦岭金矿区为典型区域,辅以对采集土样重金属总量及5种形态含量的分析,开展案例研究。结果表明,基于生物可利用性与宽浓度范围的Hakanson潜在生态风险指数法能客观地揭示土壤重金属的潜在生态风险,具有更大的适应性,是一种有效的潜在生态风险评价方法。  相似文献   

Estimate of heavy metals in soil and streams using combined geochemistry and field spectroscopy in Wan-sheng mining area,Chongqing, China     

《International Journal of Applied Earth Observation and Geoinformation》2015

Heavy metals contaminated soils and water will become a major environmental issue in the mining areas. This paper intends to use field hyper-spectra to estimate the heavy metals in the soil and water in Wan-sheng mining area in Chongqing. With analyzing the spectra of soil and water, the spectral features deriving from the spectral of the soils and water can be found to build the models between these features and the contents of Al, Cu and Cr in the soil and water by using the Stepwise Multiple Linear Regression (SMLR). The spectral features of Al are: 480 nm, 500 nm, 565 nm, 610 nm, 680 nm, 750 nm, 1000 nm, 1430 nm, 1755 nm, 1887 nm, 1920 nm, 1950 nm, 2210 nm, 2260 nm; The spectral features of Cu are: 480 nm, 500 nm, 610 nm, 750 nm, 860 nm, 1300 nm, 1430 nm, 1920 nm, 2150 nm, 2260 nm; And the spectral features of Cr are: 480 nm, 500 nm, 610 nm, 715 nm, 750 nm, 860 nm, 1300 nm, 1430 nm, 1755 nm, 1920 nm, 1950 nm. With these features, the best models to estimate the heavy metals in the study area were built according to the maximal R². The R² of the models of estimating Al, Cu and Cr in the soil and water are 0.813, 0.638, 0.604 and 0.742, 0.584, 0.513 respectively. And the gradient maps of these three types of heavy metals’ concentrations can be created by using the Inverse distance weighted (IDW).The gradient maps indicate that the heavy metals in the soil have similar patterns, but in the North-west of the streams in the study area, the contents are of great differences. These results show that it is feasible to predict contaminated heavy metals in the soils and streams due to mining activities by using the rapid and cost-effective field spectroscopy.  相似文献   

Physico-chemical Speciation of Lead in South San Francisco Bay     

P.B. Kozelka  S. Sañudo-Wilhelmy  A.R. Flegal  K.W. Bruland 《Estuarine, Coastal and Shelf Science》1997,44(6):649-658

The speciation of lead at a site in the South San Francisco Bay was determined using a combination of physical size fractionation and electrochemical analyses. The ‘ total dissolvable ’ Pb was 8·1 nM from analysis of an acidified unfiltered sample. The ‘ dissolved ’ Pb was equal to 0·20 nM (41 ng l⁻¹), only 2·5% of the ‘ total dissolvable ’ Pb. The difference yielded the ‘ particulate ’ Pb equal to 7·9 nM (1·6 μg l⁻¹). Results from crossflow ultrafiltration indicated that almost all (0·19 nM) of the dissolved Pb was ‘ in solution ’ [<10K nominal molecular weight (MW)] and that colloidal Pb (10K MW to 0·2 μm)accounted for onlyc. 1% of the dissolved Pb at this station. This small concentration (0·01 nM) of colloidal Pb may be attributed to the low amount of organic carbon associated with colloid size fraction as determined by dissolved organic carbon analyses.The chemical speciation of lead was determined in the dissolved sample and ultrafiltered sub-sample. Differential pulse anodic stripping voltammetry (DPASV) on a thin mercury film (TMF) rotating glassy carbon disk electrode (RGCDE) was used to distinguish the kinetically labile inorganic species (Pb′) from the Pb-chelated by organic ligands (PbL_i). Lead titration results were similar for both samples revealing that Pb′, PbL_iand excess unbound ligands were present primarily in the ultrafiltrate, rather than in the colloidal phase. The titration data can be interpreted as dissolved Pb being influenced by two classes of Pb-binding ligands. In the dissolved sample, the concentration of the stronger class of ligands was [L₁]=0·89±0·35 nM, with a conditional stability constant ofK^cond_L1,Pb′=3±1×10¹⁰M⁻¹. The weaker class was [L₂]=12·8±1·9 nM, withK^cond_L1,Pb′=4±1×10⁸ M⁻¹. The presence of these ligands, in excess of the dissolved Pb, resulted in [Pb′]=7±2 pM and [Pb²⁺]=0·3 pM (62 pg l⁻¹). While less than 2·4% of the ambient Pb was ‘ in solution ’, it existed chiefly in the form of organic complexes with [PbL₁]=0·15 nM and [PbL₂]=0·03 nM. More significantly, there were large concentrations of unchelated Pb-binding ligands, (L_i′), available to buffer the free Pb²⁺concentration in the event of perturbations in dissolved Pb.  相似文献