Groundwater components in the alluvial aquifer of the alpine Rhone River valley, Bois de Finges area, Wallis Canton, Switzerland

Source, type, and quantity of various components of groundwater, as well as their spatial and temporal variations were determined by different hydrochemical methods in the alluvial aquifer of the upper Rhone River valley, Bois de Finges, Wallis Canton, Switzerland. The methods used are hydrochemical modeling, stable-isotope analysis, and chemical analysis of surface water and groundwater. Sampling during high- and low-water periods determined the spatial distribution of the water chemistry, whereas monthly sampling over three years provided a basis for understanding seasonal variability. The physico-chemical parameters of the groundwater have spatial and seasonal variations. The groundwater chemical composition of the Rhone alluvial aquifer indicates a mixing of weakly mineralized Rhone River water and SO₄-rich water entering from the south side of the valley. Temporal changes in groundwater chemistry and in groundwater levels reflect the seasonal variations of the different contributors to groundwater recharge. The Rhone River recharges the alluvial aquifer only during the summer high-water period. Electronic Publication     

Ammonium geochemistry of some Mexican silver deposits

Lithogeochemical sampling in the Guanajuato, Pachuca and Tayoltita silver mining districts of Mexico has revealed the presence of significant ammonium anomalies related to mineralized veins. The anomalies can be recognised in surface as well as in mine crosscut and drill core samples and persist over depths of several hundreds of metres. Ammonium haloes are best developed in the hanging walls of major veins but anomalous concentrations are also found in footwall regions. In all three areas ammonium is an effective pathfinder for epithermal precious-metal vein-style mineralization. Comparison with data for major and trace elements (Ca, K, Mg, Na, As, Ba, Cu, P, Rb, S, Sb, Sr, Zn) shows that ammonium often forms broader haloes with a more consistent relationship to the veins than other lithogeochemical indicators. Variations in ammonium geochemistry between deposits can be related to the availability of ammonium in the epithermal system, wall-rock lithology and the nature of the vein network.The results of this study suggest that ammonium geochemistry has considerable potential as an exploration tool for precious-metal vein deposits.     

Changes in groundwater chemistry due to metallurgical activities in an alluvial aquifer in the Moa area (Cuba)

The aim of this work is to evaluate the changes in groundwater chemistry in an alluvial aquifer in the Moa area. Surface and ground water, metallurgical waste and various geological material samples were collected in order to evaluate groundwater composition. The results show that the alluvial aquifer is polluted with SO₄^2-, Mg²⁺and heavy metals. According to its major components in the alluvial aquifer, two types of groundwater are identified: magnesi-bicarbonated and sulphate-magnesic. Maximum SO₄^2– and Mg²⁺ contents are more than 1000 mg/L, and are four times higher than the acceptable levels for human consumption of water. The high values of Cr(VI), Ni(II), Mn(II) Fe_(total), SO₄^2– and Mg²⁺ in alluvial aquifers are due to polluted recharge from metallurgical waste from the tailing dam. This recharge is favoured by the preferential flow due to desiccation cracks in metallurgical waste. Geochemical modelling showed that potentially toxic heavy metals might exist largely in the forms of MSO₄^2– and M²⁺ in pore water of SAL metallurgical waste. All samples were supersaturated in goethite and hematite. Results from batch testing indicate that the heavy metals have two origins: natural, due to the existing ultramaphic rocks and laterites, and anthropogenic, by metallurgical waste rich in sulphate and (oxy)hydroxide minerals. These results highlight the need to locate and evaluate a new water source to supply the population of the city of Moa.     

Testing the 14C ages and conservative behavior of dissolved 14C in a carbonate aquifer in Yucca Flat,Nevada (USA), using 36Cl from groundwater and packrat middens

Corrected groundwater ¹⁴C ages from the carbonate aquifer in Yucca Flat at the former Nevada Test Site (now the Nevada National Security Site), USA, were evaluated by comparing temporal variations of groundwater ³⁶Cl/Cl estimated with these ¹⁴C ages with published records of meteoric ³⁶Cl/Cl variations preserved in packrat middens (piles of plant fragments, fecal matter and urine). Good agreement between these records indicates that the groundwater ¹⁴C ages are reasonable and that ¹⁴C is moving with chloride without sorbing to the carbonate rock matrix or fracture coatings, despite opposing evidence from laboratory experiments. The groundwater ¹⁴C ages are consistent with other hydrologic evidence that indicates significant basin infiltration ceased 8,000 to 10,000 years ago, and that recharge to the carbonate aquifer is from paleowater draining through overlying tuff confining units along major faults. This interpretation is supported by the relative age differences as well as hydraulic head differences between the alluvial and volcanic aquifers and the carbonate aquifer. The carbonate aquifer ¹⁴C ages suggest that groundwater velocities throughout much of Yucca Flat are about 2 m/yr, consistent with the long-held conceptual model that blocking ridges of low-permeability rock hydrologically isolate the carbonate aquifer in Yucca Flat from the outlying regional carbonate flow system.     

Groundwater geochemistry of a small reservoir catchment in Central Tunisia

Due to the scarcity of water resources in semiarid sedimentary basins, hill reservoirs are often constructed to recharge groundwater and limit runoff induced water loss. The impact of such reservoirs on groundwater chemistry is investigated in the aquifers of the El Gouazine watershed, Central Tunisia. Three groundwater types are recognised, Ca–HCO₃, Na–Cl and Ca–SO₄. The strong similarity between host rock and groundwater chemistries indicates significant rock–water interaction. A flowpath, along which the chemical composition of the groundwater evolves, can be identified using the contrast in stable isotope signature between upstream and downstream groundwater. Shallow upstream groundwater is recharged by the infiltration of rainwater with the rate of recharge strongly linked to the permeability of the host lithology. Calcium and HCO₃ are supplied to an alluvial aquifer from a more rapidly recharged limestone aquifer with the concentration of Ca and HCO₃ ions decreasing by dilution. The alluvial aquifer is also enriched in Ca and SO₄ during the downstream flow of groundwater through gypsiferous materials. There is evidence of mixing between meteoric groundwater and evaporated reservoir water. Below the reservoir and partly responsible for reservoir leakage is a sandy aquifer, formed by weathering and erosion of a sandstone host which also supplies water to the alluvial aquifer.     

Geochemistry and Cr stable isotopes of Cr-contaminated groundwater in León valley,Guanajuato, México

León valley, located in the Mexican state of Guanajuato, has a long history (35+ a) of Cr contamination of groundwater and surface water. Here data are presented for Cr, major ion and trace element concentrations and Cr stable isotope measurements of groundwater in a heavily contaminated aquifer in Buenavista, where Cr ore processing residue piles (COPRPs) located in a chromate production factory are the main source of Cr. The aquifer directly beneath the factory still retains very high Cr(VI) concentrations (∼121 mg/L). Ongoing pump and treat remediation is keeping the high concentration plume confined to the factory area and immediate vicinity, though Cr is also detected at some distance away. Chromium isotope data of the aquifer directly under the factory show only a small increase in δ⁵³Cr (+0.33‰ to +0.81‰) and indicates minimal reduction of Cr(VI) to Cr(III). Very high Cr(VI) concentrations have possibly overwhelmed natural reductants and furthermore fresh Cr(VI) was being leached into the groundwater from the COPRP. From just one year of Cr isotope data it is clear that more aggressive remediation techniques will be necessary to reduce or eliminate the contamination. The fringes of the Cr plume have substantially lower concentrations and can be partially explained by transport of the main plume or mixing between waters from the nearby landfill and highly contaminated waters from QC. While the source of Cr at the fringes of the plume could be attributed to a source from the nearby landfill instead of the main plume from the factory, the Cr stable isotope data show enrichment in the heavier isotopes and point to varying amounts of reduction. Isotopic enrichment seen between 2007 and 2008 along the fringe may indicate either reduction or less unreacted Cr(VI) is being transported to the fringes. In either case some potential for natural attenuation of Cr(VI) exists at the western margin of the plume with the landfill playing a role.     

Arsenic and metal mobility from Au mine tailings in Rodalquilar (Almería,SE Spain)

In the old mining area of Rodalquilar, mine wastes, soil and sediments were characterized and the results revealed high concentration of Au, Ag, As, Bi, Cu, Fe, Mn, Pb, Se, Sb and Zn in tailings and sediments. The contaminant of greatest environmental concern is As. The mean concentration in the tailings was 679.9, and 345 mg/kg in the sediments of Playazo creek. The groundwater samples from the alluvial aquifer showed high concentration of Al, As, Cd, Fe, Hg, Mn, Ni, Pb, Se, Sb and Zn and very high concentration of chloride and sulfate, which were above the concentration defined in the European standards for drinking water. The presence of As in groundwater may be caused by the oxidation of arsenian pyrite, the possible As desorption from goethite and ferrihydrite and the jarosite dissolution. Groundwater concentrations of Cd, Fe, Mn, and possibly Cu, were associated with low values of Eh, indicating the possible dissolution of oxy-hydroxides of Fe and Mn. The mobility of metals in the column experiments show the release of Al, Fe, Mn, Cr, Cu, Ni, V and Zn in significant concentrations but below the detected values in groundwater. However, As, Cd, Sb, Se Pb and Au, are generally mobilized in concentrations above the detected values in groundwater. The possible mass transfer processes that could explain the presence of the contaminants in the aquifer and the leachates was simulated with the PHREEQC numerical code and revealed the possible dissolution of the following mineral phases: jarosite, natrojarosite, arsenian pyrite, alunite, chlorite, kaolinite and calcite.     

Arsenic content and groundwater geochemistry of the San Antonio-El Triunfo, Carrizal and Los Planes aquifers in southernmost Baja California, Mexico

 The San Antonio-El Triunfo mining district, located at a mountainous region 45 km south-east of La Paz, Baja California, has been worked since the late 1700s. Mine waste material produced during 200 years of mineral extraction area poses a risk of local groundwater pollution and eventually, regional pollution to the Carrizal (west basin) and the Los Planes (east basin) aquifers. There are different types of deposits in the mining area. These are dominated by epithermal veins, in which arsenopyrite is an important component. Carrillo and Drever (1998a) concluded that, even though the amount of mine waste is relatively small in comparison to the large scale area, significant As in groundwater derived from the mine waste piles is found locally in the groundwater. This paper shows the results of geochemical analyses of groundwater samples from the San Antonio-El Triunfo area and the Carrizal and Los Planes aquifers during several years of monitoring (1993–1997). The highest values of total dissolved solids (TDS) and As are in the mineralized area where the mining operations occurred (∼1500 ppm TDS and 0.41 ppm As). The lowest concentrations of TDS and As are, in general, away from the mineralized area (∼500 ppm TDS and 0.01 ppm As). Sulfate and bicarbonate (alkalinity) are, in general, high near the mineralized area and low away from it. The arsenic concentrations vary seasonally, especially after the heavy summer thunderstorms. Geochemical modeling (MINTEQA2 and NETPATH) and analysis of the regional geochemical evolution of the groundwater from the mining area towards the aquifer of Los Planes shows that the most likely hydrochemical processes include: dilution, precipitation of calcite, and adsorption of As onto surfaces of iron oxyhydroxides (ferrihydrite). These processes act as natural controls to the extent and amount of As pollution in the Carrizal and Los Planes aquifers. Received: 4 May 1999 · Accepted: 22 February 2000     

浅成低温热液金银多金属矿床矿化分带及找矿标志

自20世纪70年代环太平洋地区发现大批浅成低温热液型矿床以来,浅成低温热液矿床业已成为贵金属矿床和Cu、Pb、Zn等有色金属矿床的重要工业类型。文章依据主要工业组分对我国浅成低温热液Au、Ag多金属矿床进行了分类,并讨论了成矿系列及矿化分带特征,即按成矿深度浅成低温热液Au、Ag多金属矿床自下而上可分为:Au-Cu/Cu-Au矿床;Au/Au(Ag)矿床;Au-Ag矿床;Ag/Ag多金属矿床;Pb-Zn-Ag矿床。同时,根据我国浅成低温热液Au、Ag多金属矿床特征尝试性提出了浅成低温热液型银矿床的成矿规律与找矿标志。     

Hydrogeologic characteristics of the alluvial tuff aquifer of northern Sahand Mountain slopes, Tabriz, Iran

The Tabriz area is a densely populated area of northwestern Iran (more than 1.5 million in population) with a large proportion of its drinking, domestic, industrial and agricultural water supplied from groundwater resources. The average rate of drinking and industrial water use in the city of Tabriz is about 3.45 m³ s^–1. The Plio-Pleistocene unconfined alluvial tuff aquifer (about 1,275 km²), the most important aquifer in the area, has been known for many years as a reliable resource. The greatest estimated thickness of the alluvial tuff lies in the Saidabad area, with 350 m thickness. There are 994 deep and 284 shallow active pumping wells and 83 qanats operate in the alluvial tuff aquifer. The total water withdrawal from all these artificial discharge points has been measured at 72, 3.8 and 17 million m3/year, respectively. Analytical and numerical methods have been applied to the constant rate pumping test data from the Saidabad wellfield (eight pumping and three observation wells). The values of electrical conductivity in the groundwater of alluvial tuff aquifer range from 203 to 960 μS cm^–1 and bicarbonate type water dominates.     

Optimization of water resources management using SWOT analysis: the case of Zakynthos Island, Ionian Sea, Greece

Zakynthos, an island of 408 km² in the Ionian Sea, is completely dependent on its groundwater resources for fulfilling the demands of the water supplies. The use of groundwater resources has become particularly intensive during the last decades because of the intense urbanization, the tourist development and the irrigated land expansion that took place. The main aquifers are developed in limestones (karstic), sandstones of neogene deposits (confined) and alluvial deposits (phreatic). This paper focuses on the assessment of their hydrogeological characteristics and the groundwater quality. For this investigation, groundwater level measurements, drilling data, pumping tests and chemical analyses of groundwater samples were used. The average annual consumption that is abstracted from the aquifer systems, is 4.9 × 10⁶ m³ year⁻¹. The exploitable groundwater reserves were estimated to be 3.3 × 10⁶ m³ year⁻¹. In the last decades, the total abstractions exceed the natural recharge, due to the tourist development; therefore the aquifer systems are not used safely. The results of chemical analyses showed a deterioration of the groundwater quality. According to the analyses the shallow alluvial aquifer and the confined aquifer are polluted by nitrates at concentrations in excess of 25 mg L⁻¹. High sulphate concentrations might be related to the dissolution of gypsum. Seawater intrusion phenomena are recorded in coastal parts of aquifer systems. The increased Cl⁻ concentrations in karstic aquifer indicate signs of overexploitation. Strengths, weaknesses, opportunities and threats (SWOT) analysis was applied in order to evaluate the SWOT of the groundwater resources. Moreover, some recommendations are made to assist the rational management that aim at improving the sustainability of the groundwater resources of Zakynthos Island.     

Investigation of the hydrogeochemical processes in an alluvial channel aquifer located in a typical Karoo Basin of Southern Africa

An investigation was conducted to assess the hydrogeochemical processes of an alluvial channel aquifer located in a typical Karoo Basin of Southern Africa. The investigation was aimed at identifying and describing the groundwater chemistry evolution and its contribution to the overall groundwater quality. X-ray fluorescent spectrometry (XRF) and X-ray diffractometry (XRD) analyses were performed on geological samples to identify and quantify the major element oxides and minerals. The study utilises the conventional Piper diagram, bivariate plots and PHREEQC hydrogeochemical model to analyse groundwater chemistry data obtained during the wet (February and May) and dry seasons (August and December) of 2011. The XRF and XRD results show that the channel deposits are dominated by SiO₂ element oxides and quartz minerals, thus elevated concentrations of silicon (Si⁴⁺) were found in the groundwater. Dolomite and calcite minerals were also detected in the unconsolidated aquifer sediments. The detailed study of the alluvial aquifer system has shown that dissolution of dolomite and calcite minerals and ion exchange are the dominant hydrogeochemical processes influencing the groundwater quality. The groundwater evolves from Ca²⁺–Mg²⁺–HCO₃ ^? recharge water that goes through ion exchange with Na⁺ in the clay-silt sediment to give a Na⁺–HCO₃ ^? water type. The groundwater is supersaturated with respect to quartz, dolomite and calcite minerals. The study shows the potential usefulness of simple bivariate plots as a complimentary tool to the conventional methods for analyzing groundwater hydrogeochemical processes.     

Malibogazi groundwater dam: an alternative model for semi-arid regions of Turkey to store and save groundwater

In central Turkey, there are serious groundwater quality problems in the main river valleys and plains, and even in the lower parts of the secondary basins due to the underlying evaporitic geological formations. Groundwater quality improves towards the upstreams in the alluvium aquifers in most secondary valleys; however, groundwater potential decreases as well due to the reduced basin area, areal extent and thickness of the aquifers. The Malibogazi valley is situated to some 100 km north of Ankara. The dam constructed in the narrowest section of the valley has an average storage coefficient of 0.2 and the total and active storage capacities of 110,000 and 55,000 m³, respectively. The 20-m-thick aquifer extends for 6–7 km till the dam site within valley with an average width of 50–70 m. It mostly comprises sandy–gravely alluvial deposits. Malibogazi groundwater dam is a valve-controlled gravity flow dam. When the valves are opened, the water from the aquifer reservoir flows by gravity through supply pipe to the main irrigation channel, but when the valves are closed the water is stored in the aquifer and groundwater level begins to rise. Average groundwater discharge was about 20 l/s in 2005–2006 irrigation period. In this period, groundwater levels were about 2 m higher compared to the groundwater levels in the same seasons before the construction of the groundwater dam. Because the dam is of gravity flow type, it means an important contribution to the farmers since the operation cost is quite low. Malibogazi groundwater dam represents one of the first experiences of Turkey in the field of groundwater storage. Although the dam has small storage capacity, it may be a model for Turkey from the viewpoints of investigation, construction, dam wall, intake facility and measurements etc.     

Hydrological connectivity of alluvial Andean valleys: a groundwater/surface-water interaction case study in Ecuador

The Andean region is characterized by important intramontane alluvial and glacial valleys; a typical example is the Tarqui alluvial plain, Ecuador. Such valley plains are densely populated and/or very attractive for urban and infrastructural development. Their aquifers offer opportunities for the required water resources. Groundwater/surface-water (GW–SW) interaction generally entails recharge to or discharge from the aquifer, dependent on the hydraulic connection between surface water and groundwater. Since GW–SW interaction in Andean catchments has hardly been addressed, the objectives of this study are to investigate GW–SW interaction in the Tarqui alluvial plain and to understand the role of the morphology of the alluvial valley in the hydrological response and in the hydrological connection between hillslopes and the aquifers in the valley floor. This study is based on extensive field measurements, groundwater-flow modelling and the application of temperature as a groundwater tracer. Results show that the morphological conditions of a valley influence GW–SW interaction. Gaining and losing river sections are observed in narrow and wide alluvial valley sections, respectively. Modelling shows a strong hydrological connectivity between the hillslopes and the alluvial valley; up to 92 % of recharge of the alluvial deposits originates from lateral flow from the hillslopes. The alluvial plain forms a buffer or transition zone for the river as it sustains a gradual flow from the hills to the river. Future land-use planning and development should include concepts discussed in this study, such as hydrological connectivity, in order to better evaluate impact assessments on water resources and aquatic ecosystems.     

The impact of tailings dam spills and clean-up operations on sediment and water quality in river systems: the Rı́os Agrio–Guadiamar,Aznalcóllar,Spain

The Aznalcóllar tailings dam at Boliden Apirsa's Aznalcóllar/Los Frailes Ag–Cu–Pb–Zn mine 45 km west of Seville, Spain, was breached on 25 April 1998, flooding approximately 4600 hectares of land along the Rı́os Agrio and Guadiamar with approximately 5.5 million m³ of acidic water and 1.3×10⁶ m³ of heavy metal-bearing tailings. Most of the deposited tailings and approximately 4.7×10⁶ m³ of contaminated soils were removed to the Aznalcóllar open pit during clean-up work undertaken immediately after the spill until January 1999. Detailed geomorphological and geochemical surveys of the post-clean-up channel, floodplain and valley floor, and sediment and water sampling, were carried out in January and May 1999 at 6 reaches representative of the types of river channel and floodplain environments in the Rı́o Guadiamar catchment affected by the spill. The collected data show that the clean-up operations removed enough spill-deposited sediment to achieve pre-spill metal (Ag, As, Cd, Cu, Pb, Sb, Tl, Zn) concentrations in surface sediment. These concentrations, however, are still elevated above pre-mining concentrations, and emphasise that mining continues to contaminate the Agrio-Guadiamar river system. Dilution by relatively uncontaminated sediment appears to reduce metal concentrations downstream but increases in metal and As concentrations occur downstream, presumably as a result of factors such as sewage and agriculture. River water samples collected in May 1999 have significantly greater dissolved concentrations of metals and As than those from January 1999, probably due to greater sulphide oxidation from residual tailings with concomitant release of metals in the warmer early summer months. These concentrations are reduced downstream, probably by a combination of dilution and removal of metals by mineral precipitation. Single chemical extractions (de-ionised water, CaCl₂ 0.01 mol l⁻¹, CH₃COONH₄ 1 M, CH₃COONa 1 M and ammonium oxalate 0.2 M) on alluvial samples from reaches 1 and 6, the tailings, pre-spill alluvium and marl have shown that the order of sediment-borne contaminant mobility is generally Zn>Cd>Cu>Pb>As. Pb and As are relatively immobile except possibly under reducing conditions. Much of the highly contaminated sediment remaining in the floodplain and channel still contains a large proportion of tailings-related sulphide minerals which are potentially reactive and may continue to release contaminants to the Agrio–Guadiamar river system. Our work emphasises the need for pre-mining geomorphological and geochemical data, and an assessment of potential contributions of contaminants to river systems from other, non-mining sources.     

Groundwater flow in a transboundary fault-dominated aquifer and the importance of regional modeling: the case of the city of Querétaro,Mexico

The city of Querétaro, located near the political boundary of the Mexican states of Querétaro and Guanajuato, relies on groundwater as it sole water supply. Groundwater extraction in the city increased from 21?×?10⁶ m³/yr in 1970 to 104?×?10⁶ m³/yr in 2010, with an associated drawdown of 100 m in some parts of the aquifer. A three-dimensional numerical groundwater-flow model has been developed that represents the historical evolution of the aquifer’s potentiometric levels and is used to simulate the effect of two scenarios: (1) a 40 % reduction in the extraction rate from public water supply wells in early 2011 (thus reducing the extraction to 62?×?10⁶ m³/yr), and (2) a further reduction in 2021 to 1?×?10⁶ m³/yr. The modeling results project a temporary recovery of the potentiometric levels after the 40 % reduction of early 2011, but a return to 2010 levels by 2020. If scenario 2 is implemented in 2021, the aquifer will take nearly 30 years to recover to the simulated levels of 1995. The model also shows that the wells located in the city of Querétaro started to extract water from part of the aquifer beneath the State of Guanajuato in the late 1970s, thus showing that the administrative boundaries used in Mexico to study and develop water resources are inappropriate, and consideration should be given to physical boundaries instead. A regional approach to studying aquifers is needed in order to adequately understand groundwater flow dynamics.     

Mineralogical and geochemical behavior of mill tailing material produced from lead-zinc skarn mineralization,Hanover, Grant County,New Mexico,USA

Mineral extraction and processing, especially metal mining, produces crushed and milled waste; such material, exposed to weathering, poses the potential threat of environmental contamination. In this study, mill tailings from inactive Pb-Zn mines in New Mexico, southwest USA, have been examined for their potential environmental impacts by means of detailed mineralogical and geochemical characterization. The principal ore minerals remaining in the tailings material are sphalerite, chalcopyrite, and very minor galena, smithsonite, and cerrusite, accompanied by the gangue minerals pyrite, pyrrhotite, magnetite, hematite, garnet, pyroxene, quartz, and calcite. White precipitate occurring on tailings surfaces is composed of gypsum and hydrated magnesium sulfates. Pyrite is mostly unaltered or shows only micron-scale rims of oxidation (goethite/hematite) in some surface samples. This iron oxide rim on pyrite is the only indication of weathering-derived minerals found by microscopy. There are variations in element concentrations with depth that reflect primary variations through time as the tailings ponds were filled. Cadmium and Zn concentrations increase with depth and Ag and Pb are low for the uppermost core samples, while Cu, Ni, and Co concentrations are generally high for the uppermost core samples. These elemental distributions indicate that little or no leaching has taken place since emplacement of the tailings because no accumulation or enrichment of these metals is observed in Hanover tailings, even in reducing portions of tailings piles. Element concentrations of surface samples surrounding the tailings reflect underlying mineralized zones rather than tailings-derived soil contamination. We observed no successive decreasing metal concentrations in prevalent wind directions away from the tailings. Stream sediment samples from Hanover Creek have somewhat elevated Zn, Cd, and Pb concentrations in areas that receive sediments from erosion of the tailings. However, input from tributaries downstream of the ponds appears to be principal source of heavy metals in Hanover Creek. The results of this study indicate that there is low risk for groundwater heavy-metal contamination from Hanover tailings. Tailings material do not show significant geochemical oxidation/alteration or metal leaching with depth. Our studies indicate that neutralizing minerals present in the tailings are sufficient to keep the tailings material chemically stable. Geochemically, however, tailings materials are being eroded and may pose a threat to Hanover Creek via siltation.     

Evaluation of aquifer environment under Hazaribagh leather processing zone of Dhaka city

Hazaribagh is a densely populated area of Dhaka city where about 185 leather processing industries have been operating and discharging solid and liquid wastes directly to the low-lying areas, river and natural canals without proper treatment. The area is covered by alluvial deposits of Holocene age and is underlain by Pleistocene Madhupur clay. The Dupi Tila Formation of Mio-Pliocene age underlain by this yellowish gray to brick red clay bed serves as the main water-bearing aquifer of Dhaka city. To assess the environmental degradation as well as the groundwater environment, major anions, cations and heavy metals of water samples, heavy metals and organic carbon content of sediment samples were analyzed in this study. Analyses of tannery effluent detect high concentration of Na⁺, Mg²⁺, Cl⁻ and SO ₄ ²⁻ followed by Ca²⁺, NH ₄ ⁺ and K⁺ with remarkable contents of some trace elements, mainly Cr, Fe, Mn, S, Ni and Pb. Higher accumulations of Cr, Al and Fe are observed in topsoil samples with significant amounts of Mn, Zn, Ni and Cu. Concentrations of ions and all the investigated trace elements of sampled groundwater were within the maximum allowable limit for drinking water of the Department of Environment, Bangladesh (DoE), and World Health Organization (WHO). However, excessive concentrations of Cr, Pb, etc., have already been reported in the shallow groundwater (10–20 m) of the area. Due to excessive withdrawal the vulnerability of groundwater contamination in deeper parts cannot be avoided for the future.     

Water management for acid mine drainage control at the polymetallic Zn–Pb–(Ag–Bi–Cu) deposit Cerro de Pasco, Peru

The geochemical and mineralogical study of the Quiulacocha tailings impoundment has shown that the hydrological connection of the three studied mine-waste systems at Cerro de Pasco (Pyrite-rich waste-rock dump Excelsior, old tailings impoundment Quiulacocha, and the active tailings impoundment Ocroyoc) is a critical concern for effective acid mine drainage (AMD) control and mine-waste management. The Quiulacocha tailings covered 114 ha, comprising 79 Mt of tailings, which contained  50 wt.% pyrite, and are located at 4340 m altitude in a tropical puna climate with about 1025 mm/a rainfall and 988 mm/a of evaporation. The tailings were partially overlain by the Excelsior waste-rock dump, which contains about 26,400,000 m³ of waste rocks that cover 94 ha and contained  60 wt.% of pyrite, which origin from a massive pyrite-quartz replacement body. Therefore, these two mine-waste deposits had a direct hydrological connection, resulting in the export of AMD produced at Excelsior towards Quiulacocha. In the Quiulacocha impoundment there are two different types of tailings recognized, that interact with the AMD from Excelsior: 1) Zn–Pb-rich tailings and 2) Cu–As-rich tailings. During the sampling, the Zn–Pb-rich part of Quiulacocha was not producing important excesses of AMD from the oxidation zone, since the pH increased to near neutral values at 1 m depth. The underlying tailings were still able to neutralize the acidity produced in the oxidation zone through sulfide oxidation by the carbonates (mainly dolomite and siderite) contained in the Zn–Pb mineral assemblage. The main source of AMD in this mine-waste system is the Excelsior waste-rock dump. Its acid seepage infiltrates into Quiulacocha forming a Fe–Zn–Pb plume with a pH 5.5–6.1 and containing up to 7440 mg/L Fe, 627 mg/L Zn, and 1.22 mg/L Pb. The plume was detected at 10–13 m depth in the stratigraphy of Quiulacocha tailings. Additionally, the AMD seepage outcropping at the base of the Excelsior waste-rock dump was channeled on the tailings surface into the Quiulacocha pond (pH 2.3), which covered the Cu–As-rich tailings. Infiltration of this Fe(III)-rich AMD increased tailings oxidation in the southwestern part of the impoundment, and subsequently liberated arsenic by enargite oxidation. Additionally, the AMD collected in the Quiulacocha pond was pumped into the active Ocroyoc tailings impoundment, where sulfide oxidation was strongly enhanced by the input of dissolved Fe(III). Therefore, the AMD management and a hydrological separation of the different mine-waste systems could be a first step to prevent further extension of the AMD problem in order to prevent increased sulfide oxidation by Fe(III)-rich solutions.     

Tracing ionic sources and geochemical evolution of groundwater in the Intermountain Una basin in outer NW Himalaya,Himachal Pradesh,India

The present research aims to identify sources of ions and factors controlling the geochemical evolution of groundwater in an intermountain basin, comprising hill and valley fill region, of Outer Himalaya in Himachal Pradesh, India. The groundwater samples collected from 81 tubewells and handpumps are analyzed for major ions, trace metals and stable isotopes (δ¹⁸O and δD). Geochemically the dominant hydrochemical facies in the Una basin are Ca–HCO₃, Ca–Mg–HCO₃ and Na–Cl types at few locations. A relatively lower ionic concentration in the valley fills indicates dilution and low residence time of water to interact with the aquifer mass due to high porosity and permeability. The ionic ratios of 0.9, 0.8 and 3.8 to 5.7, respectively, for (Ca?+?Mg): HCO₃, (Ca?+?Mg): (HCO₃?+?SO₄) and Na: Cl, suggests that ionic composition of groundwater is mainly controlled by rock weathering of, particularly by dissolution/precipitation of calcrete and calcite hosted in rock veins and Ca–Na feldspar hosted in conglomerate deposits derived from the Higher and Lesser Himalaya during the formation of Siwalik rocks. Although Na, K, NO₃ and SO₄ are introduced in the groundwater through agricultural practices, Na has also been introduced through ion exchange processes that have occurred during water–rock interaction, as indicated by negative CAI values. Factor analysis further suggests three major factors affecting the water chemistry of the area. The first two factors are associated with rock weathering while the third is anthropogenic processes associated with high nitrate and iron concentration. High concentrations of Fe and Mn ions that are exceeded that of WHO and BIS standards are also present at few locations. The recharge of groundwater in the Outer Himalaya is entirely through Indian Southwest Monsoon (ISM) and depleted ratios of δ¹⁸O/δD in valley region indicate infiltration from irrigation in recharging the groundwater and fractionation of isotopes of precipitation due to evaporation before infiltration. High d-excess values and inverse relation with δ¹⁸O are indicative of secondary evaporation of precipitation during recharge of groundwater.