Distribution and behavior of heavy metals in a river polluted by acid mine drainage in the Dabaoshan mine area, China

Acid mine drainage （AMD） has been recognized as a major environmental pollution problem over past decades. This pollutant effluent is complex and is characterized by elevated concentrations of iron and sulfate, low pH, and high concentrations of a wide variety of metals depending on the host rock geology. Massive inadvertent discharges from acid mines have given rise to dramatic cases of ecological damage. These events indicate an improved understanding of the mechanism controlling metal transport to the river is important, since the aquatic ecology will be affected, to some degree, dependent on the phase （dissolved or particulate） in which the metal is transported. In this study, polluted water samples were collected along the Hengshi River near the Dabaoshan mine, Guangdong, China, in April 2005. The concentrations of dissolved Cu, Zn, Cd and Pb have been determined using ICP-MS and the chemical speciation of those metals in suspended particles was examined using BCR methods and SEM/EDX mineralogical analysis. Combining these two sets of data, the intention was to develop geochemical concepts, which explain the behavior of Cu, Zn, Cd and Pb in particle-water interactions of heavy metals in AMD. The results show that the dissolved heavy metals exhibited non-conservative behavior in the Hengshi River. The dissolved and particulate Cu, Zn, Cd and Pb have the similar spatial distribution, which decreased gradually along the river except in the lower reaches because of the absorption-desorption between dissolved and particulate phases. Although the metal concentrations in both phases were elevated, dissolved metals were dominant and had the maximum concentrations in the low pH region.     

Origin and residence time of salinity in the Äspö groundwater system

The origin of salinity within the Äspö groundwater system is investigated by combining interpretations of conservative dissolved ions and of stable isotope ratios in water. The interpretation concludes that the groundwater salinity results from a mixing between Baltic Sea water intrusion and a deep seated saline groundwater of marine origin. This conclusion supports the geochemical model developed for the Äspö site. The residence time of the deep salinity is assessed by comparing the ³⁶Cl content of dissolved salt at different depths and the secular equilibrium value of the host rock. The ³⁶Cl of deepest levels corresponding to the highest salinity, is in equilibrium with rock, suggesting a penetration of the deep salinity into the host rock more than 1.5 Ma ago.     

Impacts of acid mine drainage on a stream in subtropical China during a major flood event

Field and laboratory work was carded out to investigate the chemistry and ecotoxicity of stream water affected by acid mine drainage in a tributary catchment of the Pearl River in subtropical China during a major flood event that corresponded to a return period of 100 years occurred in the study area. The results indicate that stream water was affected by acid mine drainage from the Dabaoshan Mine at least to a distance of 25 km downstream of the mine water discharge point. It appears that sulfide-H^＋ from the waste rock dumps was readily available for discharging and the amount of H^＋ being transported outwards depended on the volume of out-flowing waters. However, there was a lag time for the discharge of the metals. This may be attributed to the slower release of metals, relative to H^＋, because it might take more time for the dissolution of heavy metal-bearing compounds. Fe, Zn and Al were the major metals of potential toxicity contained in the AMD-affected stream water, followed by Mn, Cu, Pb, As, Cd and Ni. Acute toxicity tests show that the AMD-affected stream water at 3.5 km downstream of the discharge point was highly toxic to the test organisms.     

Mercury in river sediments, floodplains and plants growing thereon in the drainage area of the Idrija mine, Slovenia

Half a millennium mercury production at Idrija is reflected in increased mercury contents in all environmental segments. The bulk of roasting residues from the middle of the 19th century to 1977 was discharged directly into the Idrijca River, and the material was carried at high waters to the Soca River and farther into the Adriatic Sea. It has been estimated that 45500 tons of mercury were emitted into the environment during the operating period of the mine, which ceased production in 1994. In the lower reaches of the Idrijca the riverine deposits with high mercury contents have been, and will be in the future a source of mercury polluted sediment. Stream sediments were monitored at the same locations along the Idrijca and Soca rivers （70 kin） every 5 years since 1991 （1991-2005）. Grain size distribution was determined by dry sieving and fractions for geochemical analysis were prepared （〈0.04 and 〈0.125 mm）. Soils on river terraces were sampled at 5 localities in the lower course of Idrijca. At two locations of the terrace profiles the samples of averaged meadow forage and plantain （Plantago lanceolata） were collected within a 50-meters radius. We found that there was no decrease in mercury concentration in active river sediments during the last 20 years. Upstream from the Idrija Town the mercury concentrations in active river sediments vary from 1 to 10 mg/kg （average 3.3 mg/kg）. From Idrija to Spodnja Idrija the mercury concentrations increase extremely and vary greatly （32-4,121 mg/kg, the average is 734 mg/kg）. From Spodnja ldrija to the Idrijca-Soca confluence is the average 218 mg/kg, and 57 mg/kg downstream in the Soca River sediments.     

Geological controls and effects of floodplain asymmetry on river–groundwater interactions in the southeastern Coastal Plain, USA

Channel sediment and alluvial aquifer hydraulic properties exert a major control on river–groundwater interactions. Channels and floodplains are often asymmetrical, resulting in differences in sediment hydraulic properties across the river. Floodplain asymmetry is common along Coastal Plain rivers in South Carolina and North Carolina, USA. The Tar River, North Carolina, has an asymmetrical valley. The study objective was to characterize the effects of floodplain asymmetry and geological controls on river–groundwater interactions. Floodplain and river channel sediments adjacent to the river were characterized with split spoon cores and hand auger samples along a 22-km reach. Hydrogeology was characterized with 38 piezometers and water level recorders in and adjacent to the river. Ground penetrating radar was used to define the shallow stratigraphy. Channel sediments were significantly different between the north and south sides of the river. Hydraulic conductivity and groundwater inputs were greater on the side of the river (north) that contained more permeable fluvial deposits. Groundwater chemistry (δ¹⁸O, specific conductance) data also suggested greater exchange between surface water and groundwater on the north side of the river channel. A conceptual hydrogeological model illustrates that groundwater movement and contaminant transport to the river differs across the channel due to asymmetrical geology.     

Modes,hydrodynamic processes and ecological impacts exerted by river–groundwater transformation in Junggar Basin,China

The hydrodynamic processes and impacts exerted by river–groundwater transformation need to be studied at regional and catchment scale, especially with respect to diverse geology and lithology. This work adopted an integrated method to study four typical modes (characterized primarily by lithology, flow subsystems, and gaining/losing river status) and the associated hydrodynamic processes and ecological impacts in the southern part of Junggar Basin, China. River–groundwater transformation occurs one to four times along the basin route. For mode classification, such transformation occurs: once or twice, controlled by lithological factors (mode 1); twice, impacted by geomorphic features and lithological structures (mode 2); and three or four times, controlled by both geological and lithological structures (modes 3 and 4). Results also suggest: (1) there exist local and regional groundwater flow subsystems at ~400 m depth, which form a multistage nested groundwater flow system. The groundwater flow velocities are 0.1–1.0 and?<0.1 m/day for each of two subsystems; (2) the primary groundwater hydro-chemical type takes on apparent horizontal and vertical zoning characteristics, and the TDS of the groundwater evidently increases along the direction of groundwater flow, driven by hydrodynamic processes; (3) the streams, wetland and terminal lakes are the end-points of the local and regional groundwater flow systems. This work indicates that not only are groundwater and river water derived from the same source, but also hydrodynamic and hydro-chemical processes and ecological effects, as a whole in arid areas, are controlled by stream–groundwater transformation.     

Dynamics of greenhouse gases in the river–groundwater interface in a gaining river stretch (Triffoy catchment,Belgium)

This study investigates the occurrence of greenhouse gases (GHGs) and the role of groundwater as an indirect pathway of GHG emissions into surface waters in a gaining stretch of the Triffoy River agricultural catchment (Belgium). To this end, nitrous oxide (N₂O), methane (CH₄) and carbon dioxide (CO₂) concentrations, the stable isotopes of nitrate, and major ions were monitored in river and groundwater over 8 months. Results indicated that groundwater was strongly oversaturated in N₂O and CO₂ with respect to atmospheric equilibrium (50.1 vs. 0.55 μg L^?1 for N₂O and 14,569 vs. 400 ppm for CO₂), but only marginally for CH₄ (0.45 vs. 0.056 μg L^?1), suggesting that groundwater can be a source of these GHGs to the atmosphere. Nitrification seemed to be the main process for the accumulation of N₂O in groundwater. Oxic conditions prevailing in the aquifer were not prone for the accumulation of CH₄. In fact, the emissions of CH₄ from the river were one to two orders of magnitude higher than the inputs from groundwater, meaning that CH₄ emissions from the river were due to CH₄ in-situ production in riverbed or riparian zone sediments. For CO₂ and N₂O, average emissions from groundwater were 1.5?×?10⁵ kg CO₂ ha^?1 year^?1 and 207 kg N₂O ha^?1 year^?1, respectively. Groundwater is probably an important source of N₂O and CO₂ in gaining streams but when the measures are scaled at catchment scale, these fluxes are probably relatively modest. Nevertheless, their quantification would better constrain nitrogen and carbon budgets in natural systems.     

Using environmental tracers to assess the extent of river–groundwater interaction in a quarried area of the English Chalk

The Swanscombe area of Kent, SE England represents a typical example of a heavily quarried Chalk area currently undergoing re-development. Because the Chalk is also an important aquifer, a good understanding of groundwater movement is required if environmental impacts are to be minimised and the water resource maximised. In particular, the nature of the relationship between the River Darent and groundwater in the Swanscombe Chalk Block requires better characterisation. Here, ‘environmental tracers’ in the form of ambient concentrations of stable isotopes, chlorofluorocarbons (CFCs), sulphur hexafluoride (SF₆) and tritium (³H) are used to investigate this and other aspects of groundwater movement in the vicinity of the quarries. Stable isotopic contrasts indicate little evidence for widespread river infiltration to the regional Chalk aquifer, although stable isotope and ³H data suggest that 20–35% of the abstraction by river-valley public water supply boreholes may be derived from the river. The CFCs, while present at above-modern concentrations in almost all groundwaters, can be used as tracers, indicating basically S–N flowpaths in the area south of the quarries, though sub-karstic conduits associated with areas of Palaeogene cover add a level of uncertainty at the local scale. Simple piston flow residence times based on SF₆ range from 1 to 17 a, but the data are probably better interpreted in terms of mixing between varying amounts of modern recharge derived from the south and deeper stored groundwater. The information gained from environmental tracers can therefore contribute to effective resource management.     

Groundwater hydrochemistry and soil pollution in a catchment affected by an abandoned lead–zinc mine: functioning of a diffuse pollution source

The importance of polluted alluvial soils as a potential diffuse source of heavy metals was investigated in a catchment of the Matylda stream affected by an abandoned lead and zinc ore mine in Upper Silesia, southern Poland. This was attempted by means of standard groundwater analyses performed together with measurements of Cd, Pb, Zn, Fe and Mn concentrations in soil and groundwater. The Matylda stream, receiving mine water, was converted in the 20th century into a straight channel directed in its middle reach over the valley bottom. This changed the drainage direction of the Matylda stream water. During mining operations, groundwater seepage, combined with surface drainage by shallow ditches caused pollution of sandy soils exceeding over 100 mg/kg of Cd, 24% of Zn and 4% of Pb at surface or subsurface soil horizons, and reaching at least 60 cm in depth. After mine closure in the 1970s, the network of ditches appears to be a source of Ca, Mg, chlorides, carbonates and nitrates, as indicated by the more or less regular increase of these major ion concentrations in groundwater down ditches. Whereas, the ditches are a sink rather than a source of zinc, cadmium and lead in permanently dry reaches, or transition zones in reaches with surface water flowing periodically. The metal concentrations and distribution in soil and groundwater suggest the slow mobilization of heavy metals stored in the valley bottom and the minor importance of soil as a diffuse source for surface water pollution.     

Contamination of water and soil by the Erdenet copper–molybdenum mine in Mongolia

As one of the largest copper–molybdenum (Cu–Mo) mines in the world, the Erdenet Mine in Mongolia has been active since 1978 and is expected to continue operations for at least another 30 years. In this study, the potential impacts of mining activities on the soil and water environments have been evaluated. Water samples showed high concentrations of sulfate, calcium, magnesium, Mo, and arsenic, and high pH values in the order of high to low as follows: tailing water > Khangal River > groundwater. Statistical analysis and the δ²H and δ¹⁸O values of water samples indicate that the tailing water directly affects the stream water and indirectly affects groundwater through recharge processes. Soil and stream sediments are highly contaminated with Cu and Mo, which are major elements of ore minerals. Based on the contamination factor (CF), the pollution load index (PLI), and the degree of contamination (C_d), soil appears to be less contaminated than stream sediments. The soil particle size is similar to that of tailing materials, but stream sediments have much coarser particles, implying that the materials have different origins. Contamination levels in stream sediments display a tendency to decrease with distance from the mine, but no such changes are found in soil. Consequently, soil contamination by metals is attributable to wind-blown dusts from the tailing materials, and stream sediment contamination is caused by discharges from uncontained subgrade ore stock materials. Considering the evident impact on the soil and water environment, and the human health risk from the Erdenet Mine, measures to mitigate its environmental impact should be taken immediately including source control, the establishment of a systematic and continuous monitoring system, and a comprehensive risk assessment.     

Modified acid–base accounting model validation and pH buffer trend characterisation in mine drainage at the AngloGold Ashanti Obuasi mine in Ghana,West Africa

Acid–base accounting (ABA) is a static test used to evaluate pre-mining drainage quality of ores with interpretations based on a reference 3-data point model. The method is often complemented with a kinetic test to ensure certainty of results. The challenges associated with both methods compel companies to rely on only the ABA test, thereby compromising on the long-term drainage quality. This paper validates a proposed 4-data point model that was used to establish a 20% increase in the alkaline amendment of ores at the AngloGold Ashanti Obuasi Mine in Ghana. The validation was done using model limits, the robustness of coefficient of determination and model factor sequence variation. Acidification trends and mineralogical data evaluation of tailings were used to characterise pH buffer trends in mine drainage. The modified 4-data point model, which incorporates a vital kinetic test factor into the ABA model, provides a criterion for the adjustment of carbonate amendment value to improve acid neutralisation in the drainage; this would reduce (1) cost of experimentation, (2) turnaround time for analyses, (3) complexities associated with both test methods. From the XRD data, alunite and goethite are present in tailings to provide sustained pH buffering in drainage beyond the scope of the modified model, while the characterised pH buffer trend could be used for monitoring drainage quality.     

Different types of fine-grained sediments associated with acid mine drainage in the Libiola Fe–Cu mine area (Ligurian Apennines,Italy)

Different types of fine-grained chemical precipitates were characterized in the surroundings of the pyrite-chalcopyrite mine of Libiola (Northern Italy). Both water chemistry and sediment composition were used to investigate metal mobility near the mine area. Local drainage waters were very acidic (with a pH as low as 2.5) and were rich in dissolved metals (Fe, Al, Cu, Zn, Mn, Ni). Sediments associated with low pH water (pH <4.5) were ochreous mixtures of schwertmannite and goethite with traces of jarosite. Their chemistry was dominated by Fe and they had, compared to other sediments investigated, low concentrations of other metals. When the acidity decreased gradually, other precipitates formed. At a pH of approximately 5, a poorly crystalline, whitish, Al-rich precipitate occurred. At a pH between 6 and 7, a poorly crystalline, blue, Cu (Zn) rich phase was present. These “sequential” precipitation events progressively reduced the metal loading typical of the acidic mine water when there was a gradual mixing with normal water. When a sudden mixing between normal waters (pH ∼8, Ca–HCO₃, low metal bearing) and acidic waters took place, a rapid flocculation occurred of mixed precipitates containing Fe, Al and trace elements.     

Quantification of the water balance and hydrogeological processes of groundwater–lake interactions in the Pampa Plain, Argentina

This paper gives an account of the assessment and quantification of the water balance and the hydrogeological processes related to lake–groundwater interaction in the Pampa Plain by using hydrogeochemical, isotopic and flow numerical modeling techniques. La Salada is a permanent shallow lake, with an area of 5.8 km², located on the SE of Buenos Aires Province. A total of 29 lake water samples and 15 groundwater samples were collected for both hydrochemical analysis and environmental stable isotope determination. Water table depths were measured in wells closed to the lake. Groundwater samples appear grouped on the Local Meteoric Water Line, suggesting a well-mixed system and that rainfall is the main recharge source to the aquifer. Water evaporation process within La Salada is also corroborated by its isotopic composition. The model that best adjusts to La Salada Lake hydrochemical processes includes evaporation from groundwater, calcite precipitation with CO₂ release and cationic exchange. The annual water balance terms for the lake basin indicates for each hydrological component the following values: 1.16 E⁰⁸ m³ rainfall, 8.15 E⁰⁷ m³ evapotranspiration, 1.90 E⁰⁶ m³ runoff, 1.55 E⁰⁷ m³ groundwater recharge, 6.01 E⁰⁶ m³ groundwater discharge to the lake, 9.54 E⁰⁶ m³ groundwater discharge to the river, 5.00 E⁰⁵ m³ urban extraction and 4.90 E⁰⁶ m³ lake evaporation. Integrated analysis of hydrochemical and isotopic information helped to calibrate the groundwater flow model, to validate the conceptual model and to quantitatively assess the basin water balance.     

Investigation of pyrite oxidation and acid mine drainage characterization associated with Razi active coal mine and coal washing waste dumps in the Azad shahr–Ramian region,northeast Iran

Acid mine drainage (AMD) pollution is considered to be the most serious water pollution problem in mining areas. AMD containing iron sulfates and other components can affect the receiving water bodies. Pyrite oxidation and AMD generation can be considered as important processes that may take place in the wastes produced by coal mining and coal washing operations in the Golestan province (northeast Iran). The study area is characterized by appropriate atmospheric conditions that favor pyrite oxidation and the presence of a large amount of water bodies. This study attempts to consider pyrite oxidation and AMD generation in the Azad shahr–Ramian region. The impact of AMD on the quality of the surface water bodies was investigated by taking samples and analyzing them for hydro-geochemical parameters. Stiff and Piper diagrams were used to represent chemical analyses of water samples. The coal samples taken from different depths at four points on two different coal waste dumps were analyzed to find the fraction of pyrite that remained in the waste particles to investigate the pyrite oxidation process. A computational fluid dynamic package called PHOENICS was used to model pyrite oxidation process numerically. The results obtained from the geochemical analyses of water and coal samples and numerical simulation show pyrite oxidation and acid generation in the region. However, the presence of carbonate rocks raised the pH of the water samples. The drainages of the Razi mine may be recognized as natural alkaline mine drainages.     

Major types and time–space distribution of Mesozoic ore deposits in South China and their geodynamic settings

The ore deposits of the Mesozoic age in South China can be divided into three groups, each with different metal associations and spatial distributions and each related to major magmatic events. The first event occurred in the Late Triassic (230–210 Ma), the second in the Mid–Late Jurassic (170–150 Ma), and the third in the Early–Mid Cretaceous (120–80 Ma). The Late Triassic magmatic event and associated mineralization is characterized by peraluminous granite-related W–Sn–Nb–Ta mineral deposits. The Triassic ore deposits are considerably disturbed or overprinted by the later Jurassic and Cretaceous tectono-thermal episodes. The Mid–Late Jurassic magmatic and mineralization events consist of 170–160 Ma porphyry–skarn Cu and Pb–Zn–Ag vein deposits associated with I-type granites and 160–150 Ma metaluminous granite-related polymetallic W–Sn deposits. The Late Jurassic metaluminous granite-related W–Sn deposits occur in a NE-trending cluster in the interior of South China, such as in the Nanling area. In the Early–Mid Cretaceous, from about 120 to 80 Ma, but peaking at 100–90 Ma, subvolcanic-related Fe deposits developed and I-type calc-alkaline granitic intrusions formed porphyry Cu–Mo and porphyry-epithermal Cu–Au–Ag mineral systems, whereas S-type peraluminous and/or metaluminous granitic intrusions formed polymetallic Sn deposits. These Cretaceous mineral deposits cluster in distinct areas and are controlled by pull-apart basins along the South China continental margin. Based on mineral assemblage, age, and space–time distribution of these mineral systems, integrated with regional geological data and field observations, we suggest that the three magmatic–mineralization episodes are the result of distinct geodynamic regimes. The Triassic peraluminous granites and associated W–Sn–Nb–Ta mineralization formed during post-collisional processes involving the South China Block, the North China Craton, and the Indo-China Block, mostly along the Dabie-Sulu and Songma sutures. Jurassic events were initially related to the shallow oblique subduction of the Izanagi plate beneath the Eurasian continent at about 175 Ma, but I-type granitoids with porphyry Cu and vein-type Pb–Zn–Ag deposits only began to form as a result of the breakup of the subducted plate at 170–160 Ma, along the NNE-trending Qinzhou-Hangzhou belt (also referred to as Qin-Hang or Shi-Hang belt), which is the Neoproterozoic suture that amalgamates the Yangtze Craton and Cathaysia Block. A large subduction slab window is assumed to have formed in the Nanling and adjacent areas in the interior of South China, triggering the uprise of asthenospheric mantle into the upper crust and leading to the emplacement of metaluminous granitic magma and associated polymetallic W–Sn mineralization. A relatively tectonically quiet period followed between 150 and 135 Ma in South China. From 135 Ma onward, the angle of convergence of the Izanagi plate changed from oblique to parallel to the coastline, resulting in continental extensional tectonics and reactivation of regional-scale NE-trending faults, such as the Tan-Lu fault. This widespread extension also promoted the development of NE-trending pull-apart basins and metamorphic core complexes, accompanied by volcanism and the formation of epithermal Cu–Au deposits, granite-related polymetallic Sn–(W) deposits and hydrothermal U deposits between 120 and 80 Ma (with a peak activity at 100–90 Ma).     

Hydrogeochemical characteristics of groundwater and pore-water and the paleoenvironmental evolution in the past 3.10 Ma in the Xiong’an New Area,North China

The groundwater level has been continuously decreasing due to climate change and long-time overexploitation in the Xiong’an New Area, North China, which caused the enhanced mixing of groundwater in different aquifers and significant changes in regional groundwater chemistry characteristics. In this study, groundwater and sediment pore-water in drilling cores obtained from a 600 m borehole were investigated to evaluate hydrogeochemical processes in shallow and deep aquifers and paleo-environmental evolution in the past ca. 3.10 Ma. Results showed that there was no obvious change overall in chemical composition along the direction of groundwater runoff, but different hydrochemical processes occurred in shallow and deep groundwater in the vertical direction. Shallow groundwater (< 150 m) in the Xiong’an New Area was characterized by high salinity (TDS > 1000 mg/L) and high concentrations of Mn and Fe, while deep groundwater had better water quality with lower salinity. The high TDS values mostly occurred in aquifers with depth < 70 m and >500 m below land surface. Water isotopes showed that aquifer pore-water mostly originated from meteoric water under the influence of evaporation, and aquitard pore-water belonged to Paleo meteoric water. In addition, the evolution of the paleoclimate since 3.10 Ma BP was reconstructed, and four climate periods were determined by the δ¹⁸O profiles of pore-water and sporopollen records from sediments at different depths. It can be inferred that the Quaternary Pleistocene (0.78–2.58 Ma BP) was dominated by the cold and dry climate of the glacial period, with three interglacial intervals of warm and humid climate. What’s more, this study demonstrates the possibilities of the applications of pore-water on the hydrogeochemical study and further supports the finding that pore-water could retain the feature of paleo-sedimentary water.© 2021 China Geology Editorial Office.     

The tectono-magmatic evolution of the West Junggar terrane (NW China) unravelled by U–Pb ages of detrital zircons in modern river sands

ABSTRACT

The West Junggar terrane (WJT) is an outstanding laboratory for studying the tectonic evolution of the Junggar–Balkhash Ocean, because it contains widespread Paleozoic magmatism in different tectonic settings. We attempt to reconstruct the tectono-magmatic evolution of WJT through U–pb analysis of detrital zircons from three modern river sand samples from the Harabura, Baibuxie, and Aletengyemule rivers in the Barleik Mountains of the central WJT. A total of 232 concordant spots show Th/U ratios of 0.14–1.69, typical of igneous origin, and they contain abundant Paleozoic (96%) and few Precambrian (4%) ages, with major age populations at 450–530, 400–430, 320–380, and 265–320 Ma. The first two groups may be derived from the early subduction- and accretion-related magmatic rocks of the WJT, whereas the third group is congruent with magmatic activities related to the final subduction and basin-filling processes within a framework of the remnant Junggar–Balkhash Ocean. By combining with the regional data, the last group of magmatic events is referred to as post-subduction magmatism. The missing Mesozoic–Cenozoic magmatism clearly indicates a pre-Permian closure for the Junggar–Balkhash Ocean, nearly coeval with the closure of other oceans in the southwestern Palaeo-Asian Ocean.     

Evolution of the magmatic–hydrothermal system and formation of the giant Zhuxi W–Cu deposit in South China

The Zhuxi deposit is a recently discovered W–Cu deposit located in the Jiangnan porphyry–skarn W belt in South China. The deposit has a resource of 3.44 million tonnes of WO3, making it the largest on Earth,however its origin and the evolution of its magmatic–hydrothermal system remain unclear, largely because alteration–mineralization types in this giant deposit have been less well-studied, apart from a study of the calcic skarn orebodies. The different types of mineralization can be classified into magnesian skarn, calcic skarn, and scheelite–quartz–muscovite(SQM) vein types. Field investigations and mineralogical analyses show that the magnesian skarn hosted by dolomitic limestone is characterized by garnet of the grossular–pyralspite(pyrope, almandine, and spessartine) series, diopside, serpentine,and Mg-rich chlorite. The calcic skarn hosted by limestone is characterized by garnet of the grossular–andradite series, hedenbergite, wollastonite, epidote, and Fe-rich chlorite. The SQM veins host highgrade W–Cu mineralization and have overprinted the magnesian and calcic skarn orebodies. Scheelite is intergrown with hydrous silicates in the retrograde skarn, or occurs with quartz, chalcopyrite, sulfide minerals, fluorite, and muscovite in the SQM veins.Fluid inclusion investigations of the gangue and ore minerals revealed the evolution of the ore-forming fluids, which involved:(1) melt and coexisting high–moderate-salinity, high-temperature, high-pressure(>450 ℃and >1.68 kbar), methane-bearing aqueous fluids that were trapped in prograde skarn minerals;(2) moderate–low-salinity, moderate-temperature, moderate-pressure(~210–300 ℃and ~0.64 kbar),methane-rich aqueous fluids that formed the retrograde skarn-type W orebodies;(3) low-salinity,moderate–low-temperature, moderate-pressure(~150–240 ℃and ~0.56 kbar), methane-rich aqueous fluids that formed the quartz–sulfide Cu(–W) orebodies in skarn;(4) moderate–low-salinity,moderate-temperature, low-pressure(~150–250 ℃and ~0.34 kbar) alkanes-dominated aqueous fluids in the SQM vein stage, which led to the formation of high-grade W–Cu orebodies. The S–Pb isotopic compositions of the sulfides suggest that the ore-forming materials were mainly derived from magma generated by crustal anatexis, with minor addition of a mantle component. The H–O isotopic compositions of quartz and scheelite indicate that the ore-forming fluids originated mainly from magmatic water with later addition of meteoric water. The C–O isotopic compositions of calcite indicate that the ore-forming fluid was originally derived from granitic magma, and then mixed with reduced fluid exsolved from local carbonate strata. Depressurization and resultant fluid boiling were key to precipitation of W in the retrograde skarn stage. Mixing of residual fluid with meteoric water led to a decrease in fluid salinity and Cu(–W) mineralization in the quartz–sulfide stage in skarn. The high-grade W–Cu mineralization in the SQM veins formed by multiple mechanisms, including fracturing, and fluid immiscibility, boiling, and mixing.     

A study of the contaminated banks of the Mahoning River, Northeastern Ohio, USA: characterization of the contaminated bank sediments and river water–groundwater interactions

The Mahoning River is one of the five most contaminated rivers in the U.S. This study characterized the contaminated sediments in the river banks and investigated the hydraulic interconnection between shallow aquifer in the banks with the river water. The study was conducted along the most polluted section of the river, which is 50-km long, using over 50 monitoring wells. The characterization part of the study investigated the sedimentology, hydraulic conductivity, and spatial distribution of the contaminated sediments. Results of the characterization revealed that the contaminated sediments consist of fine-grained sand, silt, mud, and clay. The spatial distribution of the contaminated sediment is heterogeneous and positively correlates with the hydraulic conductivity values, i.e., the greatest contamination occurs in high conductivity areas. Hydraulic conductivity was determined by the Hazen formula using 82 sediment samples. Bioremediation, which is one of the remedial options considered for the banks, is found to be hydraulically feasible because of sufficient hydraulic conductivity values (≥10^?4 cm/s) that ensure reasonable rates of nutrient delivery. Monitoring of water levels in the river and groundwater for a 10-month period shows that flow occurs from the river to groundwater and vice versa. The exchange of flow is influenced by rainfall. Flow of groundwater to the river will continually transport the dissolved contaminants in groundwater to the river. Therefore, findings of this study show that one of the remedial options that proposes dredging of channel sediments and permits no action for bank sediments cannot be chosen due to river water–groundwater interactions.     

Geochemical distribution of arsenic,cadmium, lead and zinc in river sediments affected by tailings in Zimapán,a historical polymetalic mining zone of México

High arsenic (As) groundwater is widely distributed in northwestern Hetao Plain, an arid region with sluggish groundwater flow. Observed As concentration in groundwater from wells ranges from 76 to 1,093 μg/l. Most water samples have high total dissolved solids, with Cl and HCO₃ as the dominant anions and Na as the dominant cation. The major hydrochemical types of most saline groundwaters are Na–Mg–Cl–HCO₃ and Na–Mg–Cl. By contrast, fresh groundwaters generally belong to the Na–Mg–HCO₃ type. High concentrations of arsenic in shallow aquifers are associated with strongly reducing conditions, as evidenced by high concentrations of dissolved organic carbon, ammonium, as well as dissolved sulfide and Fe, dominance of arsenite, relatively low concentrations of nitrate and sulfate, and occasionally high content of dissolved methane (CH₄). High As groundwaters from different places at Hetao Plain experienced different redox processes. Fluoride is also present in high As groundwater, ranging between 0.40 and 3.36 mg/l. Although fluorosis poses an additional health problem in the region, it does not correlate well with As in spatial distribution. Geochemical analysis indicates that evapotranspiration is an important process controlling the enrichment of Na and Cl, as well as trace elements such as As, B, and Br in groundwater. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.