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1.
 The focus of this research was to determine the impact of abandoned mines on surface water and groundwater in the historical mining districts of the Cerbat Mountains, Arizona. The surface water in the mining areas was found to be contaminated by various combinations and concentrations of heavy metals. Elevated arsenic, cadmium, and iron concentrations were detected in most surface-water samples, while lead, copper, and zinc contamination differed from region to region, depending on the ore mined. The groundwater was seriously polluted by arsenic, cadmium, lead, zinc, iron, and manganese in the immediate vicinity of mines that processed ore on the site, such as the Tennessee Mine near Chloride. Chloride's groundwater, however, showed no evidence of contamination. Three possible explanations are discussed: immobilization of the heavy metals in the soil by chemical reactions and adsorption, dilution effects due to the rainy season in spring, or the existence of different groundwater systems. Received: 17 September 1996 · Accepted: 14 May 1997  相似文献   

2.
Environmental contamination with As and Sb caused by past mining activities at Sb mines is a significant problem in Slovakia. This study is focused on the environmental effects of the 5 abandoned Sb mines on water, stream sediment and soil since the mines are situated in the close vicinity of residential areas. Samples of mine wastes, various types of waters, stream sediments, soils, and leachates of the mine wastes, stream sediments and selected soils were analyzed for As and Sb to evaluate their geochemical dispersion from the mines. Mine wastes collected at the mine sites contained up to 5166 mg/kg As and 9861 mg/kg Sb. Arsenic in mine wastes was associated mostly with Fe oxides, whereas Sb was present frequently in the form of individual Sb, Sb(Fe) and Fe(Sb) oxides. Waters of different types such as groundwater, surface waters and mine waters, all contained elevated concentrations of As and Sb, reaching up to 2150 μg/L As and 9300 μg/L Sb, and had circum-neutral pH values because of the buffering capacity of abundant Ca- and Mg-carbonates. The concentrations of Sb in several household wells are a cause for concern, exceeding the Sb drinking water limit of 5 μg/L by as much as 25 times. Some attenuation of the As and Sb concentrations in mine and impoundment waters was expected because of the deposition of metalloids onto hydrous ferric oxides built up below adit entrances and impoundment discharges. These HFOs contained >20 wt.% As and 1.5 wt.% Sb. Stream sediments and soils have also been contaminated by As and Sb with the peak concentrations generally found near open adits and mine wastes. In addition to the discharged waters from open adits, the significant source of As and Sb contamination are waste-rock dumps and tailings impoundments. Leachates from mine wastes contained as much as 8400 μg/L As and 4060 μg/L Sb, suggesting that the mine wastes would have a great potential to contaminate the downstream environment. Moreover, the results of water leaching tests showed that Sb was released from the solids more efficiently than As under oxidizing conditions. This might partly explain the predominance of Sb over As in most water samples.  相似文献   

3.
Spring water samples of the Harz Mountains were taken in several seasons of 2010, 2011, and 2012. The samples have been analysed for main components (Na+, K+, Ca2+, Mg2+, SO42−, Cl, HCO3 and NO3), trace elements (Fe, Cu, Pb, Zn, Y and REE), DOC, δ18O and δ2H of water. Meteoric water is indicated as the main source of the springs sampled. High precipitation rates lead to a dilution of the measured elemental concentrations. Furthermore, regional differences of rock and water interactions were found. REE concentrations and patterns of the spring waters vary between the distinct geological units and reflect the geochemical characteristics of the surrounding rocks. The actual data compared to measured data from the seventies and nineties of the last century indicate a decrease of the sulphate concentrations in the spring waters which is typical of many European mountain catchments.  相似文献   

4.
The Bunker Hill Mine in Idaho's Coeur d'Alene mining district produces approximately 10 m3/minute of acid water containing high concentrations of heavy metals. Field and laboratory studies indicate that much of the acid water is produced in a single ore body in the upper part of the mine. The ore of this body contains mainly sphalerite, galena, and pyrite in a siderite-quartz gangue. Ground water recharges this ore body through a near-vertical zone of high permeability, which is the result of mining by the caving technique. Ore samples from the caving area contained oxidized forms of iron and produced acid in a laboratory leaching test. Leaching experiments with several ore samples from the mine also indicated that the ratio of pyrite to calcite in the samples strongly controlled the resultant pH values. Oxidation of pyrite to sulfuric acid and compounds of iron is apparently responsible for the production of acid water in the mine. In contrast, dissolution of calcite in water results in a basic solution, with pH around 8.3, that can neutralize the acid produced by the oxidation process. Methods for prevention of acid mine drainage in this and other similar mines are noted.  相似文献   

5.
Environmental geochemistry of Zarshuran Au-As deposit, NW Iran   总被引:2,自引:1,他引:2  
Zarshuran deposit is the most famous and important As-Au mine in Iran. However, there is no information on the impact of mining activity on the surrounding environment, especially on water systems. This paper attempts to document the concentration of arsenic and associated elements in waters and sediments resulting from the mining history of Zarshuran, a period covering hundreds of years. Water and sediment samples collected from Zarshuran Stream indicate high content of some potentially toxic elements, especially of As which ranges from 0.028 to 40 ng/l in water and 182 to 36,000 mg/kg in sediment samples. Mining activity, exposure of a large volume of mining wastes to weathering, and the anomalously high background of trace metals in the mining area are considered to be the main sources of heavy metal pollution.  相似文献   

6.
Heavy metal contents have been investigated in sediment and water samples from gold and platinum mining areas of South Africa. Waste waters from Witwatersrand and Orange Free State gold mines exhibit characteristically low pH-values due to the formation of sulphuric acid by oxidation of sulphide ore minerals. Acid leaching of iron, manganese, nickel, cobalt, copper and zinc effects a 1,000–10,000-fold increase of metal concentrations as compared to the respective values in unpolluted river water. Lack of carbonate buffering prevents rapid immobilization and may lead to widespread distribution of toxic metals in the aquatic systems. These findings illustrate that modern ore refining techniques have little effect on the water quality as long as unchecked hydrometallurgical processes take place outside the production plant.  相似文献   

7.
With depleted coal resources or deteriorating mining geological conditions, some coal mines have been abandoned in the Fengfeng mining district, China. Water that accumulates in an abandoned underground mine (goaf water) may be a hazard to neighboring mines and impact the groundwater environment. Groundwater samples at three abandoned mines (Yi, Er and Quantou mines) in the Fengfeng mining district and the underlying Ordovician limestone aquifer were collected to characterize their chemical and isotopic compositions and identify the sources of the mine water. The water was HCO3·SO4-Ca·Mg type in Er mine and the auxiliary shaft of Yi mine, and HCO3·SO4-Na type in the main shaft of Quantou mine. The isotopic compositions (δD and δ18O) of water in the three abandoned mines were close to that of Ordovician limestone groundwater. Faults in the abandoned mines were developmental, possibly facilitating inflows of groundwater from the underlying Ordovician limestone aquifers into the coal mines. Although the Sr2+ concentrations differed considerably, the ratios of Sr2+/Ca2+ and 87Sr/86Sr and the 34S content of SO42? were similar for all three mine waters and Ordovician limestone groundwater, indicating that a close hydraulic connection may exist. Geochemical and isotopic indicators suggest that (1) the mine waters may originate mainly from the Ordovician limestone groundwater inflows, and (2) the upward hydraulic gradient in the limestone aquifer may prevent its contamination by the overlying abandoned mine water. The results of this study could be useful for water resources management in this area and other similar mining areas.  相似文献   

8.
Open pit mining of base-metals from the high-sulfidation epithermal type deposit of Kirki (Thrace, NE Greece) resulted in the formation of an acid pit lake by infilling of the open cast by rain and draining waters after mine closure. The high toxic metals content of the ore, the limited buffering capacity of host rocks and the direct exposure of the ore zone to weathering result in an intense release of metals into the pit lake. The acidic and oxidative pit lake waters show high concentrations of trace metals. A mineral precipitate, covering the floor of the pit lake, comprises secondary anglesite, several species of the jarosite-group, rozenite, melanterite, wroewolfeite, gypsum, bukovskyite, beaverite, scorodite and minor goethite. The mineral precipitate presents a significant heavy metal content indicating effective removal of metals from the acid waters. Compared to other pit lakes in high-sulfidation type deposits it has a higher metal load, consistent with the mineralogy and grade of ore in pit walls.  相似文献   

9.
The beginning of iron ore mining in southern Poland dates back to very ancient times. The largest underground iron ore mine from Roman times was discovered in the northern margin of the Holy Cross Mountains, near Nowa S upia. In the seventeenth century the intensive development of iron mining occurred in this area. The iron ore mines from the Cz stochowa-Wieluń area started in the fourteenth century. Several iron ore mines in both areas worked in the 20-ies and 30-ies of the twentieth century. Since the beginning of the 70's the ore mining has been under reduction in connection with the decision of liquidation of the iron ore mining industry in Poland. The stage of the mine closure finished in 1982, when last mines closed down in the Cz stochowa-Wieluń area.  相似文献   

10.
《Applied Geochemistry》1999,14(2):147-158
This study evaluates several southern Appalachian Piedmont mining districts for Hg contamination in surface waters and determines potential relationships between Hg discharged from historical mining operations and site-specific physical factors. Water samples were collected from 3 fluvial systems that drain areas where Hg was used to amalgamate Au from ore during the 19th century. Each of the fluvial systems exhibit similar physical characteristics such as climate, vegetation, and rock type. Total Hg (HgT) determinations were made using cold vapour atomic fluorescence spectroscopy techniques. Concentrations of HgT in the southern Appalachian Piedmont range from 1–3 ng l−1 in waters of the Arbacoochee, Alabama, and South Mountains, North Carolina, Mining Districts to 13 ng l−1 in waters of the Dahlonega Mining District in Georgia. The correlation between HgT and total suspended solids (TSS) at the southern Appalachian sites was good with a coefficient of determination (r2) of 0.82. A clear trend between environmentally-available Fe (FeE) and HgT (r2=0.86) was also evident. The correlation between HgT and FeE most likely reflects similarities in the mechanisms that control the aqueous concentrations of both metals (i.e., the particle-reactive nature of the two elements), allowing for the sorption of Hg onto Fe-oxyhydroxides. Hence, increased loads of TSS from erosional events are probably responsible for higher stream water HgT concentrations. Vegetation at these sites, which is heavy due to the warm, humid climate of the SE, may help reduce the total amount of Hg released from contaminated mining sites to the rivers by controlling erosion, hence, decreasing the input of contaminated particles into streams and rivers.These southern Appalachian mining sites used Hg amalgamation techniques similar to those used in other precious metals mining districts, such as the highly contaminated Comstock Au–Ag district in Nevada, yet HgT concentrations are orders of magnitude lower; This difference in concentration between the southern Appalachian districts and the Comstock district may correlate to the relative amounts of Hg that were used in each. However, other variables were evaluated to determine if physio-chemical differences such as climate could influence HgT concentrations in surface waters of the two areas.  相似文献   

11.
为研究青藏高原金属矿山勘探、开采、闭坑阶段不同开发阶段河流重金属污染的严重程度,通过野外调查,室内测试分析,对比5个金属矿山河流重金属元素含量、污染指数沿程变化,得出以下结果:(1)勘探阶段和闭坑后河流水质污染较小,开采阶段矿业活动对河水水质污染较大。(2)As、Pb、Cd、Cu和Zn五种元素是金属矿山的特征污染物。开采矿区中德尔尼铜矿区、下柳沟铅锌矿、甲玛矿区河流均有重金属元素污染,微碱性环境中德尔尼铜矿区,主要污染物为As,单项污染指数为0~10.6;下柳沟铅锌矿Pb、Cd、Cu和Zn元素单项污染指数分别为0.2~2.1、0~55、0.4~24、0.3~1550;偏酸性环境中甲玛矿区的特征污染物主要为Cu、Cd。其中Cu、Cd单项污染指数为0~4174、0~4;勘探矿区大场金矿、闭坑矿区罗布莎铬铁矿区河流未出现污染元素。(3)青藏高原5处典型的高海拔山地矿山河流由于稀释作用重金属流经2km后达到安全水平,研究结果可为青藏高原矿山开采中河流水环境保护提供参考依据。  相似文献   

12.
Hydrogeochemical surveys were carried out in SW Sardinia (Italy) to investigate the impact of past mining activities on the quality of groundwater. The chemistry of waters from flooded galleries, adits and dumps has been compared with that of springs and wells in the same area at sites relatively far from any mine legacy. A feature, common to all waters, is the circumneutral pH, since the carbonate formations in the area neutralise the acidity produced by the oxidation of Fe-bearing sulphide minerals in the mine impacted water. However, groundwater interacting with mine workings is degraded in quality; it shows high dissolved SO4, Zn, Cd and Pb contents. In some cases groundwater exceeds the limit established by the guidelines of the World Health Organization for Pb content in drinking water, so that groundwater is mixed before entering the local aqueducts. Results from this study suggest that more attention needs to be paid to the impact on the streams from contaminated water flowing out from some mine areas because during the dry season these streams are only fed by mine groundwater. We recommend focusing efforts to reduce the chemical contamination prior to discharge.  相似文献   

13.
闽西大田地区矿床采选冶活动对水土生态环境系统造成了严重的破坏,矿区采选矿废水pH值、SO4^2-浓度远远超过水环境标准,选矿废水和接纳采选矿废水的河流水体中Fe、Mn、Cu、Pb、Zn、Cd的含量大部分超过地面5类水标准,少部分超过4类水标准,矿区采选矿业废水是地表水金属污染的重要源头。矿业废水pH值与金属Fe、Mn、Cu、Pb、Zn、Cd的含量具有明显的负相关关系,SO4^2-浓度与金属离子Fe、Mn、Cu、Pb、Zn、Cd浓度具有较一致的变化规律。提出整治硫多金属矿山环境污染,应坚持因地制宜、矿业资源开发与环境保护并重的方针,用石灰石碱性中和酸性废水,隔离覆盖尾矿矿堆,对废弃矿山植树种草进行生态修复,对效益低下的开采矿山退矿还林,对严重环境污染的矿山实行关闭,对新开矿山要进行科学规划开发。  相似文献   

14.
Uranium mining in southeastern Germany resulted in significant environmental risks. Closure of the mines and subsequent rises of water levels may result in heavy-metal and radionuclide-bearing mine waters penetrating aquifers that are used for water supply. While there are certain (geo-)technical constraints on the schedule with which flooding of the mines can proceed, this process must not result in aggravating the problem of metal release. Evaluation of the likely 'natural' geochemical situation of Königstein mine after mining has ceased, and different scenarios for the release of metals indicates that rapid flooding, albeit avoiding unnecessary aeration of the waters, is likely to result in reducing conditions and consequently low U-solubilities.  相似文献   

15.
The impact of past mining activities on the quality of groundwater and surface water has been investigated in the mining district of La Carolina (southern Spain, province of Jaén), a region characterised by the presence of mineralisations of Pb–Ag, Cu and Fe sulphides and Ba sulphates. The chemistry of waters from flooded galleries, shafts and drainage adits has been compared with that of surface waters in the same area. Generally, waters present neutral pH, since carbonates neutralise the acidity produced by the oxidation of Fe-bearing sulphide minerals in the mine impacted water. Despite of this natural attenuation process, in most of the cases, the mine groundwater is of low quality and shows high dissolved SO4 (up to 3.7 g/l), Fe and Mn contents (tens to hundreds mg/l), exceeding the limit established by the guidelines of the World Health Organization for drinking water. Generally, the surface waters are of the sulphate calcium–magnesium to magnesium types, with moderate mineralisation. Post-rebound mine waters caused degradation of receiving watercourses in which the Fe contents are usually high, with values close to 3 g/l, and the mineralisation is greater as the channels run down in the mining zone. During dry seasons a considerable increase of salts and metals dissolved in stream waters was found, due to the decreasing contributions by run-off in this semiarid region, whereas the abandoned mine discharges remained practically constant.  相似文献   

16.
Transport and sediment–water partitioning of trace metals (Cr, Co, Fe, Pb, Cu, Ni, Zn, Cd) in acid mine drainage were studied in two creeks in the Kwangyang Au–Ag mine area, southern part of Korea. Chemical analysis of stream waters and the weak acid (0.1 N HCl) extraction, strong acid (HF–HNO3–HClO4) extraction, and sequential extraction of stream sediments were performed. Heavy metal pollution of sediments was higher in Chonam-ri creek than in Sagok-ri creek, because there is a larger source of base metal sulfides in the ores and waste dump upstream of Chonam-ri creek. The sediment–water distribution coefficients (K d) for metals in both creeks were dependent on the water pH and decreased in the order Pb ≈ Al > Cu > Mn > Zn > Co > Ni ≈ Cd. K d values for Al, Cu and Zn were very sensitive to changes in pH. The results of sequential extraction indicated that among non-residual fractions, Fe–Mn oxides are most important for retaining trace metals in the sediments. Therefore, the precipitation of Fe(–Mn) oxides due to pH increase in downstream sites plays an important role in regulating the concentrations of dissolved trace metals in both creeks. For Al, Co, Cu, Mn, Pb and Zn, the metal concentrations determined by 0.1 N HCl extraction (Korean Standard Method for Soil Pollution) were almost identical to the cumulative concentrations determined for the first three weakly-bound fractions (exchangeable + bound to carbonates + bound to Fe–Mn oxides) in the sequential extraction procedure. This suggests that 0.1 N HCl extraction can be effectively used to assess the environmentally available and/or bioavailable forms of trace metals in natural stream sediments.  相似文献   

17.
The Pb isotopic composition of ores is one of the important approaches to trace the ore sources.It has not yet been applied to research on bauxite ore so far.The current research on bauxite deposits in western Guangxi,China,seldom focuses on raw bauxite and studies on raw bauxite are mostly at macro-level.This study is the first to apply Pb isotope data to tracing bauxite ore sources.The Pb isotopic compositions of ore and rock samples from the Nadou and Taiping mining districts are projected on the Doe and Zartman plumbotectonic models and the results showed that the ore resources are different for the two mines.  相似文献   

18.
Several abandoned Cu mines are located along the shore of Prince William Sound, AK, where the effect of mining-related discharge upon shoreline ecosystems is unknown. To determine the magnitude of this effect at the former Beatson mine, the largest Cu mine in the region and a Besshi-type massive sulfide ore deposit, trace metal concentration and flux were measured in surface run-off from remnant, mineralized workings and waste. Samples were collected from seepage waters; a remnant glory hole which is now a pit lake; a braided stream draining an area of mineralized rock, underground mine workings, and waste piles; and a background location upstream of the mine workings and mineralized rock. In the background stream pH averaged ∼7.3, specific conductivity (SC) was ∼40 μS/cm, and the aqueous components indicative of sulfide mineral weathering, SO4 and trace metals, were at detection limits or lower. In the braided stream below the mine workings and waste piles, pH usually varied from 6.7 to 7.1, SC varied from 40 to 120 μS/cm, SO4 had maximum concentrations of 32 mg/L, and the trace metals Cu, Ni, Pb, and Zn showed maximum total acid extractable concentrations of 186, 5.9, 6.2 and 343 μg/L, respectively.  相似文献   

19.
 The Sudety Mountains contain polymetallic deposits which have been exploited since the Middle Ages. Distinct concentrations of As, Hg, F, Cr in surface water near Zloty Stok suggested that groundwater in the area could also contain elevated metal concentrations. Water samples from 15 locations including Zloty Stream, mine adit discharges, and selected springs generally show low levels of dissolved components and near-neutral pH. However, arsenic concentrations range from 0.99 mg/l to 26.16 mg/l at all 15 sample locations. Mercury concentrations were locally as high as 0.011 mg/l. These high arsenic and mercury concentrations significantly exceed water quality standards and raise concerns for using Zloty Stream for potable water. Recieved: 21 December 1998 · Accepted: 8 June 1999  相似文献   

20.
This study investigates the geochemical characteristics of the acid mine drainage discharged from the abandoned mine adits and tailing piles in the vicinity of the Lousal mine and evaluates the extent of pollution on water and on the stream sediments of the Corona stream. Atmospheric precipitation interacting with sulphide minerals in exposed tailings produces runoff water with pH values as low as 1.9–2.9 and high concentrations of (9,249–20,700 mg l−1), Fe (959–4,830 mg l−1) and Al (136–624 mg l−1). The acidic effluents and mixed stream water carry elevated Cu, Pb, Zn, Cd and As concentrations that exceed the water quality standards. However, the severity of contamination generally decreases 4 km downstream of the source due to mixing with fresh waters, which causes the dilution of dissolved toxic metals and neutralization of acidity. Some natural attenuation of the contaminants also occurs due to the general reduced solubility of most trace metals, which may be removed from solution, by either co-precipitation or adsorption to the iron and aluminium precipitates.  相似文献   

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