Summary of Deepwater Sediment/Pore Water Characterization for the Metal-laden Berkeley Pit Lake in Butte, Montana

Abstract.  Unconsolidated sediment at the bottom of the Berkeley pit lake is a mixture of detrital silicate minerals derived from sloughing of the pit walls and secondary minerals precipitated out of the water column. The latter include gypsum and K-rich jarosite. The pore waters have a similar pH to the overlying lake waters (pH 3.1 to 3.4), and have similarly high concentrations of dissolved heavy metals, including Al, Cd, Cu, Mn, Ni, and Zn. Sediment cores show that the top meter of the sediment column is moderately oxidized (jarosite-stable). Petrography, chemical analysis and geochemical modelling all suggest a transformation of poorly crystalline ferric compounds such as schwertmannite and/or ferrihydrite near the sediment surface to jarosite with depth in the core. No evidence of bacterial sulfate reduction was found in this study, despite the presence of 0.3 to 0.4 wt% organic carbon in the pit lake sediment.     

Development of the Sleeper Pit Lake

Abstract.  The Sleeper open pit gold mine operated from the mid-1980s through the mid-1990s. Operations were mostly sub-water table and extensive dewatering was required to lower groundwater levels by 180 m. Dewatering flows peaked at 930 L/s, with most flow contributed from an alluvial aquifer. After completion of mining, the pit was rapidly filled with water pumped from the alluvial aquifer to reduce the exposure time of sulfide wall rocks and waste rocks in the ultimate pit. The pumped alluvial groundwater provided a large volume of low total dissolved solids (TDS), high alkalinity water that controlled the early chemistry. The rising lake waters were amended with lime to buffer excess acidity contributed to the lake from reactive pit wall rocks during submergence. The pore water contained in submerged waste rock at the base of the pit was elevated in TDS and subsequently of higher density that the lake water. The density contrast and waste rock location limited contributions of waste rock pore water to the main body of the lake. Some stratification of the early lake occurred, with shallow water characterized by higher pH, low dissolved metals, and sulfate; deeper water had lower pH and higher dissolved metals and sulfate. The reservoir of alkalinity in the shallow layer mixed with the deeper waters and created a stabilized lake with a homogenized column that exceeded water quality expectations. Current water quality meets all Nevada primary drinking water standards with the exception of sulfate, TDS, and manganese, which are slightly elevated, as predicted. Chemistry has remained stable since development of the initial lake.     

The Chemistry of Waters Associated with Metal Mining in Macedonia

Abstract  Pollution from current and past mining is a significant problem in several parts of the former Yugoslav Republic of Macedonia. Water from six different mining areas in Macedonia was analysed to assess the effects of metalliferous mining activities. Drainage sediments at all locations show evidence of physical and chemical contamination; water compositions, however, were more variable. Low pH water associated with mining has led to the dissolution of minerals and the mobilization of metals from the ores and the host rocks. Only Sb was noted to exhibit enhanced mobility in higher pH waters. The Zletevo Pb-Zn mine discharges low pH water that has high levels of several metals, including Al, Zn, Cd, and Fe; sediment concentrations are grossly elevated for several km downstream. Toranica and Sasa Pb-Zn mines exhibit similar sediment contamination of Pb, Zn, Cd, and other ore-related metals. However, concentrations of metals in waters are far lower at both of these mines, due to less pyrite in the ore and the buffering of the acid waters by carbonate host lithologies. At the Buchim copper mine, waters are both acidic and high in dissolved solids; Cu concentrations exceed 100 mg/L. Krstov Dol and Alshar are small, disused As-Sb mines that discharge waters that exceed potable values for some contaminants (e. g. As), but this may be related to the mineralization of the bedrock rather than the mines. In general, metal concentrations decreased downstream from the source due to dilution from other rivers and coprecipitation of metals on other mineral phases (e. g. Fe-, Al- and Mn-oxides, and hydroxides).     

Geochemistry of Perched Water in an Abandoned Underground Mine, Butte, Montana

Abstract.  The Lexington tunnel is the last accessible underground mine working in the Butte, Montana mining district. Used as recently as 1993, the tunnel and adjacent workings have been abandoned for over 10 years. Although the Lexington tunnel is over 200 m above the regional water table, perched water is present over much of its extent. Mine water near the portal is moderately acidic (pH 4 to 5), with extremely high concentrations of metals, including Cu (up to 1000 mg/L) and Zn (up to 1400 mg/L). In the middle reaches of the tunnel, the quality of the water is much better, with near-neutral pH, high bicarbonate alkalinity, and lower concentrations of heavy metals. The low acidity and metal content is attributed to a lack of pyrite and other sulfides in this portion of the mine, as well as the presence of carbonate minerals, such as rhodochrosite (MnCO₃), in exposed veins. Sulfide minerals are more widespread further back in the tunnel, and are now oxidizing rapidly, leading to pockets of severe acid drainage (pH< 3, dissolved Zn up to 5000 mg/L). Geochemical modeling suggests that the near-neutral waters—the most voluminous type encountered in the Lexington tunnel—are close to equilibrium saturation with rhodochrosite and hydrous Zn-carbonate (ZnCO₃•H₂O). The Eh of these waters is most likely controlled by redox reactions involving dissolved Mn²⁺ and secondary, Zn-rich, hydrous Mn-oxides. In contrast, the Eh of the acidic waters appears to be controlled by reactions involving Fe²⁺ and Fe³⁺. Most of the acidic waters are saturated with K-jarosite, which forms delicate, straw-like dripstones at several localities. Decaying mine timbers could be an important renewable source of organic carbon for heterotrophic microorganisms, such as iron- and sulfate-reducing bacteria, especially deeper in the mine workings where the ground is saturated with anoxic ground water.     

Pollution of Water and Stream Sediments Associated with the Vale De Abrutiga Uranium Mine,Central Portugal

Abstract.   The Vale de Abrutiga uranium deposit, located in Central Portugal near the Aguieira dam reservoir, was surface mined. Low-grade ore and waste rock were deposited on permeable ground, close to the mine, and were not revegetated. A lake has formed in the open pit. Surface waters draining the mine site are acidic, have high conductivity, and high concentrations of U, SO42-, Zn, Fe, Mn, Ra, Cu, Th, and Pb. The groundwater and the water from the reservoir cannot be used for human consumption or irrigation. The sampled waters show higher contaminant concentrations in winter than in summer. Stream sediments have high geoaccumulation indices for U, Fe, Ag, Zn, Cr, Co, and Pb. In general, sediments bordering the dam reservoir have higher metal contents in winter than in summer.     

Microbial Alkalinity Production to Prevent Reacidification of Neutralized Mining Lakes

Abstract.  Microbial alkalinity production was evaluated as a method to prevent reacidification of neutralized mining lakes by acidic ground and seepage water. We used 60 L mesocosms to represent the sediment and water column of a shallow acidic mine lake. To enhance alkalinity production, acidic and neutralized lake waters were treated with either phosphorus (controlled eutrophication) or organic matter (controlled saprobization). Controlled eutrophication could not produce enough autochthonous biomass as substrate for microbial alkalinity production to change the acidity of the water. Chemical pre-neutralization of the acidic water caused the inorganic carbon concentration to increase, but at the same time, hindered algae growth by reducing the availability of phosphate by sorption to the freshly precipitated iron hydroxide. This effect was so strong that even high phosphorus additions could not increase the algae biomass production. In contrast to controlled eutrophication, controlled saprobization produced significant alkalinity. Despite inhibition of the most important alkalinity producing process, namely microbial sulfate reduction, by low pH values, the microbial alkalinity production rate was not affected by pre-neutralization of the water column. Other alkalinity producing processes raised the pH in the reactive zone until sulfate reduction was no longer inhibited.     

Waste from Biodiesel Manufacturing as an Inexpensive Carbon Source for Bioreactors Treating Acid Mine Drainage

Abstract.  Alcohol-fed, semi-passive bioreactors have been used to support the growth of sulfate-reducing bacteria (SRB) for treatment of acid drainage from mine sites. An alcohol source not previously examined for use in these reactors is the glycerol-methanol waste remaining after the production of biodiesel fuel. In the laboratory, rock-filled columns were used to investigate biodiesel waste (BDW) as a carbon source for SRB. Columns were provided with water containing 900 mg/L sulfate, and fed reagent-grade glycerol or BDW in sufficient quantity to reduce 50% of the sulfate. Addition of 246 mg/L of reagent-grade glycerol resulted in 50% sulfate reduction and production of up to 59 mg/L of soluble sulfide, while the equivalent of 246 mg/L of glycerol provided as BDW resulted in 55% sulfate reduction and the production of up to 92 mg/L of soluble sulfide. During the initial stages of acclimation, propionic, acetic, formic, and lactic acids were observed. Acid concentrations were reduced over time in the effluent, and organic carbon in the BDW was nearly completely converted to carbon dioxide.     

The Limnology of Summer Camp Pit Lake: A Case Study

Abstract.  Surface water bodies are expected to form in several pits at the Getchell Open Pit Mine after mining has ceased due to inflowing surface and ground water. Predicting the long-term geochemical behavior of the pit water is important in assessing potential environmental effects. One of the pits, the Summer Camp Pit, began to develop a pit lake in 1991 when dewatering ceased and the pit was used to store water pumped from underground operations. This provided a field-scale opportunity to identify the controls on lake water chemistry and determine the effects of seasonal mixing events on long-term chemical behavior. During a five-year period (1996-2001), a number of physical, chemical and mineralogical characteristics of the lake were monitored with the intent of using this information as a basis for predicting long-term geochemical behavior of future lakes in the other pits. Seasonal and multiyear cycles were identified within the water column. These cycles were influenced by climatic changes and element and sediment loadings of inflow to the lake. Stratification occurred, with the metalimnion or active layer of the lake evolving from a low total dissolved solids (TDS), alkaline water to a high TDS, neutral to mildly acidic water, until turnover occurred due to density variations between the metalimnion and epilimnion, completely mixing the layers. A hypolimnion that formed has the potential to stabilize metals in the basal sediments as sulfide minerals below a chemolimnion in the lake. Longer-term events also appear to involve the hypolimnion.The monitoring program demonstrated the dynamic nature of a pit lake and how the complex limnology can affect seasonal water quality. Such considerations are important in interpreting water quality from pit lakes and in selecting monitoring data to use when constructing mathematical models for predicting changes in water quality.     

Contaminated Alluvial Ground Water in the Butte Summit Valley

Abstract.  Ground water in alluvial sediments of upper Silver Bow Creek is chronically contaminated with heavy metals, including Cd, Cu, Fe, Mn, and Zn. Most of this contamination stems from slag, mill tailings, and waste rock from the Butte mining district that had been deposited along the ancestral Silver Bow Creek floodplain. Much of this mine waste is now buried by fill, topsoil, buildings, or parking lots. Although the pH values of most wells in the region are in the 5.5 to 7.0 range, a cluster of monitoring wells near the site of a former mill and smelter contain water that is strongly acidic (pH < 4.5), with extremely high dissolved metal concentrations (Cu up to 750 mg/L; Zn up to 490 mg/L). Ground water discharging from the area is currently collected by a subsurface French drain and conveyed to a treatment facility where lime is added to precipitate metals from solution.     

A Screening-Level Laboratory Method to Estimate Pit Lake Chemistry

Abstract.  An analog pit lake (APL) test has been developed to predict pit lake water quality following closure of an equatorial copper-gold mine. The juvenile (0-9 years after closure) pit lake (JPL) water budget will comprise 10% rainfall; 26% surface runoff; 40% wallrock runoff, and 24% deep groundwater inflow. The mature (>65 years after closure) pit lake (MPL) will consist of 39% rainfall; 29% surface runoff; 15% wallrock runoff; 3% deep groundwater inflow, and 1% shallow groundwater inflow, with the balance (13%) contributed by the JPL. Wallrock runoff due to incident precipitation was replicated in humidity columns, subaqueous wallrock leachate by leaching columns of each rock type with groundwater, rainwater by addition of sea salt to deionized water, and surface runoff by a sample from a local creek. The solutions were combined in aquaria and the appropriate fraction evaporated, 7% for the JPL and 36% for the MPL. Electron microprobe analysis of precipitates identified clays and Al, Cu, and Zn adsorbed to ferrihydrite surfaces. A preliminary pit design resulted in an acidic (pH 3.3) JPL containing 7 mg/L Cu. However, by modifying the design to exclude a potentially acidgenerating andesite unit, the JPL water quality improves (e. g., pH 6.7; Cu 0.002 mg/L). The MPL pH with the andesite would be 6.1 (Cu = 2.2 mg/L), while the final design results in a pH of 7.1 and 0.22 mg/L Cu. The APL test can also be used to corroborate numerical models predictions and assess the efficacy of mitigation alternatives.     

Geochemistry and Isotopic Composition of H2S-rich Water in Flooded Underground Mine Workings,Butte, Montana,USA

Abstract.   Groundwater being pumped from the flooded West Camp mine workings of Butte, Montana, is elevated in hydrogen sulfide (H₂S), has a circum-neutral pH, and has high arsenic but otherwise low metal concentrations. The daily flux of H₂S and As pumped from the extraction well are each estimated at roughly 0.1 kg. Isotopic analysis of coexisting aqueous sulfide and sulfate confirms that the H₂S was produced by bacterial sulfate reduction. the mine waters are close to equilibrium saturation with amorphous FeS, amorphous ZnS, siderite, rhodochrosite, calcite, and goethite, but are undersaturated with orpiment (As₂S₃). The higher solubility of orpiment relative to other mental sulfides allows concentrations of dissolved arsenic (~ 100 g/L) that are well above human health standards. The West Camp waters differ markedly from the acidic and heavy metal-rich mine waters of the nearby Berkeley pit-lake. These differences are partly attributed to geology, and partly to mining history.     

Removal of Sulphate, Metals, and Acidity from a Nickel and Copper Mine Effluent in a Laboratory Scale Bioreactor

Abstract  Mine effluents should be treated so that they can either be re-used (e. g. for mining activities or irrigation purposes) or discharged into a river system. The results of this study showed that applying laboratory scale biological sulphate removal technology to a nickel/copper mine effluent (BCL mine, Botswana) consistently lowered sulphate concentrations from an average of 2000 to 450 mg/L, and increased the pH from 5.8 to 6.5. During this period, the hydraulic retention time varied from 24 to 12 h. The Ni and Zn concentrations were reduced from a maximum of 5.86 to 0.15 mg/L and from a maximum of 38 mg/L to 0.03 mg/L, respectively, presumably precipitated as metal sulphides.     

Lake George as a Sink for Contaminants Derived from the Kilembe Copper Mining Area, Western Uganda

Abstract  The copper mine at Kilembe in the Ruwenzori Mountains in western Uganda ceased to operate in 1978 but a steady flow of contaminants, including Cu, Co, Ni, Zn, Cd, and sulphate, continues to enter the Nyamwamba-Rukoki River, which passes through Queen Elizabeth National Park, and finally flows into Lake George. Lake George is quite shallow, alkaline, and highly eutrophic. Measuring mass-flow of contaminants, water, and suspended solids in the Rukoki River near Kasese allowed us to estimate their input into Lake George. Grid sampling of lake sediments indicated that the contaminants settle near the two mouths of the river; low concentrations in a drill core in the centre of Lake George indicate that further dispersion within the lake is small. Sequential extraction experiments on lake sediments and lake water analyses suggest low bioavailability of the heavy metals. We conclude that Lake George is a highly resilient system that efficiently immobilises contaminants. Though there is no health risk for the population under present environmental conditions, a reduction of the contaminant load is desirable.     

Effects of a Barite Mine on Ground Water Quality in Andhra Pradesh,India

Abstract.  An investigation was undertaken to determine the effects of a large barite mining operation on local ground water quality near Mangampeta,Andhra Pradesh, India.Water samples were collected from drinking water wells in the mining and adjacent regions. The drinking water in the mining region had sulphate concentrations that ranged from 211 to 589 mg/L, compared to sulphate concentrations of 25 mg/L or less in the non-mined areas. The natural existence of barite and the widespread mine waste dumps at Mangampeta are believed to be responsible for the higher levels of sulphate in the ground water.     

A Survey of the Geochemistry of Flooded Mine Shaft Water in Butte, Montana

Abstract.  This paper outlines general trends in the geochemistry of the more than 10,000 km of flooded underground mine workings in the Butte mining district. The waters in question range in pH from 4 to 8, are all moderately to strongly reducing, and show a huge range in concentration of dissolved metals such as Al, As, Fe, Mn, and Zn. Metal concentrations and total acidity are highest in the Kelley mine shaft, which was the main dewatering station used to pump ground water from the underground mine complex during active mining operations. In contrast, metal concentrations are much lower in the outer portions of the district where many of the mines contain hydrogen sulfide formed by sulfate-reducing bacteria. In comparison to the other heavy metals, concentrations of Pb and Cu are quite low in the flooded mine shafts. An interesting inverse correlation between pH and water temperature is noted, which may be partly caused by exothermic pyrite oxidation reactions in the central portion of the district.     

Radionuclide Contamination of Surface Waters, Sediments, and Soil Caused by Coal Mining Activities in the ruhr District (Germany)

Abstract.   The discharge of highly mineralised mine waters with enhanced ²²⁶Ra and ²²⁸Ra activity concentrations has affected creeks, rivers, sediments, soils, and plants along the Lippe River and its tributaries. ²²⁶Ra activity concentrations were elevated in all water samples receiving mine water, with activity concentrations gradually decreasing with increased distance from the colliery due to dilution and chemical precipitation of radium with barium. Increased concentrations of radium and radium decay products were also measured in sediments and flood-affected soils. The sediments show an enrichment of ²²⁶Ra up to a factor of 750, while the contaminated soils only reach a factor of 10. In aquatic plants, a 4-fold increase in ²²⁶Ra activity concentrations was measured downstream of the discharge points. The contamination of the river banks and adjacent floodplain with radium is responsible for enhanced gamma dose rates, which, along with the incorporation of soil by playing children, provide potential radiation exposure to the public.     

Geochemical and Stable Isotope Evidence for Precipitation and Groundwater Sourcing of Recharge at the Green Valley Site,Vigo County,Indiana

Abstract  We examined the recharge sources of acid mine drainage (AMD) seeps that form at the toe of the coal refuse (gob) pile at a site in Indiana, using traditional geochemistry and oxygen isotopes. AMD from this site has impacted local waterways, and reducing the volume of AMD is a priority. Our observations indicate that there are two main sources of recharge. The first is relatively dilute, isotopically homogenous, geochemically-reducing groundwater that flows up through pre-mining karst-like features beneath the gob pile due to localized, precipitation-induced, hydraulic head. This produces a perched water table above the regional water table. The second source of recharge is oxidizing and isotopically variable meteoric precipitation that percolates through the permeable capping material; a partially buried and abandoned railroad grade may also channel meteoric waters into the pile. During periods of low precipitation, oxygenated pore moisture in the unsaturated zone facilitates AMD generation. During periods of elevated precipitation, these metal-rich pore fluids are flushed through the system by isotopically variable, oxygenated, metal-poor meteoric waters. Each source contributes subequal but variable amounts of recharge waters. The hydraulic conductivity and permeability of the gob pile, as calculated by isotopic lag, is consistent with values for silty to clean unconsolidated sand.Electronic Supplementary Material  Electronic Supplementary Material is available for this article if you access it at     

Pilot-scale Studies of Different Covers on Unoxidised Sulphide-rich Tailings in Northern Sweden: the Geochemistry of Leachate Waters

Abstract.  Leachate water quality from covered and uncovered unoxidised sulphide-rich tailings in six pilot-scale (5x5x3 m³) test cells was monitored during 2004 and 2005. The covers consisted of a layer of clayey till, sewage sludge, apatite or Trisoplast (a commercial mixture of tailings, bentonite, and a polymer). All layers were protected by an unspecified till except in one reference cell, where the tailings were left open. All leachate waters showed near-neutral pH as a result of neutralization by calcite in the tailings and by Ca(OH)₂ added prior to deposition. Average dissolved sulphur concentrations in the leachates were ≈ 600 mg L^-1, except in the cell with sewage sludge (300 mg L^-1). The source of sulphur was mainly pyrite oxidation, but residual sulphur probably remained from the enrichment process. The near-neutral pH favoured precipitation of metal-(oxy)hydroxides with subsequent removal of trace elements such as Cd, Cu and Pb (< 15 μg L^-1) from the solutions. High concentrations of Co, Mn, Ni, and Zn were found in leachates from the apatite, Trisoplast, and uncovered tailings cells. High As concentrations were found in the leachates in the sewage sludge and clayey till cells. The lowest metal concentrations, redox potential, and highest pH were found in the sewage sludge cell. Decreased elemental metal concentrations during 2004 suggest improved performance over time.     

Antimony Mobilisation and Attenuation During Ore Processing at Orogenic Gold Mines,Southern New Zealand

Mine waters at the Reefton orogenic gold mine (active from 2007 to 2016) in southern New Zealand contained dissolved arsenic (As) and antimony (Sb) up to 5 mg/L during production of a sulfide concentrate that included arsenopyrite (FeAsS) and stibnite (Sb₂S₃). Ferric oxyhydroxide adsorption extracted As down to?<?0.1 mg/L but dissolved Sb remained elevated due to adsorption competition with As. The Reefton sulfide concentrate was transported 700 km to the Macraes orogenic gold mine (active from 1990) for processing through a pressure oxidation autoclave at 225 °C. The Macraes ore has low Sb contents, so the temporary introduction of a Sb-rich component produced a short-term Sb signal in the autoclave system and tailings waters. Oxidation of stibnite occurred rapidly in the autoclave, in parallel with the As in the arsenopyrite, producing ferric antimonate (tentatively identified as As-bearing tripuhyite) and ferric arsenate (FeAsO₄). Dissolved Sb in the Macraes tailings waters remained?<?0.1 mg/L throughout the period of Reefton concentrate addition. The formation of tripuhyite in the high-temperature autoclave stabilised Sb in the Macraes tailings, so that dissolved Sb?<?As, in contrast to the low-temperature processes at Reefton where dissolved Sb?>?As.

     

Hydrogeological and Hydrochemical Characteristics of the Partially Flooded Piaseczno Opencast Sulphur Mine in Southeastern Poland

Abstract.  The basic chemical properties of Tertiary (T) and Quaternary (Q) aquifers near the Piaseczno opencast sulphur mine and the water in the open pit, along with the stratigraphy and hydrogeology of the area, were characterized to assess the feasibility of inundating the mine with ground water. Ground water quality varied markedly in the opencast area. A distinct stratification was noted in the pit water; total dissolved solids, calcium, chloride, hardness, and hydrogen sulphide increased from the top water level to the bottom of the pit lake. The concentrations of SO₄^2- and Cl^- in the opencast water were very high, especially in the hypolimnion zone. Based on our preliminary analysis, it appears that an artificial lake formed in the Piaseczno open pit could be used in the future as a fish and wildlife habitat as well as for recreational purposes.