ICP-AES在新疆哈拉奇地区水系沉积物样品分析中的应用研究

本文采用四酸溶样ICP6300电感耦合等离子体发射光谱法测试了新疆哈拉奇地区水系沉积物样品中的Li P Ti V Cr Mn Co Ni Cu Zn Sr Y Nb Mo Ba La Pb B W Sn Cd 21种微量元素,明确了该方法测试样品中的Li P Ti V Cr Mn Co Ni Cu Zn Sr Y Nb Mo Ba La 16个元素的检出限、准确度、精密度满足规范（DZ/T0130.2006-2006）要求,而Pb B Cd Sn W5个元素测试质量不能满足规范要求,并对新疆哈拉奇地区水系沉积物采样粒度样品进行了分析测试,验证了该区化探扫面选择10-80目粒度是合适的,但在异常查证工作中要选择10-60目采样粒度更合理。     

Heavy metal contamination in dust from kindergartens and elementary schools in Xi’an,China

Concentrations of As, Ba, Co, Cr, Cu, Mn, Ni, Pb, V, and Zn in campus dust from kindergartens and elementary schools in Xi’an, China, were analyzed using X-ray fluorescence spectrometry and heavy metal contamination levels were assessed based on the geoaccumulation index (I _geo), enrichment factor (EF) and numero synthesis pollution index (NSPI). The results indicate that, in comparison with Shaanxi soil, dust samples have elevated metal concentrations as a whole, except for V, Mn, Ni, and As. The assessment results of I _geo and EF indicate that V, Mn, Ni, and As in campus dust are uncontaminated, while Ba and Cr are uncontaminated to moderately contaminated, and Co, Cu, Pb, and Zn are moderately to strongly contaminated. The NSPI results show that most dust samples presented heavily contaminated by heavy metals. More attention should be paid to heavy metal contamination of campus dust from kindergartens and elementary schools of Xi’an.     

电感耦合等离子体发射光谱-逐级化学提取法研究低硫煤矸石中微量元素的赋存状态及其环境效应

煤矸石是我国堆存量最大的工业固体废物,本文应用电感耦合等离子体发射光谱法、逐级化学提取法和相关性分析研究了淮北临涣矿区低硫煤矸石中10种微量元素的含量及赋存状态,并运用风险评价指数法评价其环境效应。结果表明,低硫煤矸石中Ba、Co、Cr、Mn、Ni、Pb、V含量均高于淮北煤和中国煤均值,Mn、V的富集系数大于1,有一定迁移风险。微量元素主要以残渣态和铁锰氧化物结合态存在,两者质量分数之和为68.87%~92.93%,其中Cd、Co、Cr、Cu、Ni、Pb、Zn赋存于硫化物矿物中,V赋存于黏土矿物中,Mn赋存于碳酸盐矿物和硫化物矿物中。10种微量元素对环境的危害性大小为:MnZnNiPbCdCuBaVCrCo,表明低硫煤矸石堆存过程中活性态Mn对生态环境造成危害的可能性最大,由Mn可能引起的煤矸石山周边地区土壤及水体污染应当重视。     

Geochemical features of aerosols in Santiago de Chile from time series analysis

Santiago, the capital of Chile, suffers from high air pollution levels, especially during winter. An extensive particulate matter (PM) monitoring and analysis program was conducted to quantify elemental concentrations of PM. Size-resolved PM samples (PM_2.5 and PM_10–2.5) from the La Paz and Las Condes stations in Santiago (2004–2005) were analyzed using ICP-MS. Most trace element concentrations (Cu, Pb, Zn, Mn, V, Sb, Pb and As) were higher during winter than during summer and were also higher at the La Paz station than at the Las Condes station. During the highest pollution events, As concentrations in PM_2.5 (16 ng m^?3) exceeded the annual average standard value (6 ng m^?3). A 10-year time series showed decreasing Pb and As concentrations and slightly increasing Zn, Cu and Mn concentrations. Concentrations of Cr and Ni remained relatively constant. The implementation of new public policies in 1998 may explain the decreasing concentrations of Pb and As. Enrichment factor (EF) calculations identified two principal groups: elements with EF < 10 (Mg, Y, Zr, U Sr, Ca, Ti, and V) and EF > 10 (Rb, K, Cs, Fe, P, Ba, Mn, Ni, Cr, Co, Zn, Sn, Pb, Cu, Mo, Cd, As, Ag, and Sb), which were related to natural and anthropogenic PM sources, respectively. Three main PM sources were identified using factor analysis: a natural source (crustal matter and marine aerosol), combustion and copper smelting. Three other sources were identified using rare earth elements: fluid catalytic crackers, oil-fired power production and catalytic converters.     

Selenium and heavy metals content in some Mediterranean soils

The study of metal contents in industrial, agricultural or/and polluted soils compared with natural or unpolluted soils is currently necessary to obtain reference values and to assess soil contamination. Nonetheless, very few works published appear in international journals on elements like Se, Li and Sr in Spanish soils. This study determines the total levels of Se, Li, Sr, As, Cd, Co, Cr, Cu, Ni, Pb, V, Zn, Fe, Mn and Ba in 14 natural (unpolluted) soils (Gypsisols, Leptosols, Arenosols and Acrisols), 14 agricultural soils (Anthrosols, Fluvisols and Luvisols), and 4 industrial–urban affected-surface soil horizons (Anthrosols and Fluvisols) of Eastern Spain. The geochemical baseline concentrations (GBC) and reference values (RV) have been established, and the relationships among elements and also between soil properties and elemental concentrations have been analysed. The RV obtained in this study were (mg kg⁻¹): Se 2.68, Li 115, Sr 298, Cd 0.97, Co 35, Cr 217, Cu 46, Ni 50, Pb 137, V 120, Zn 246, Fe 124,472, Mn 2691, and Ba 743. The RV for Se and Li were used as a preliminary approach to assess soil contamination in Spanish soils. The results confirm human impact on Sr, As, Cd, Cr, Cu, Ni, Pb and Zn soil concentrations, but evidence no deviation from natural Se, Li, Co, V, Fe, Mn and Ba concentrations. The results obtained from the statistical analysis reveal significant correlations between some elements and clay and soil organic matter (SOM) contents, indicating that metal concentrations are controlled by soil composition. One particularly interesting finding is the high correlation coefficients obtained between SOM and Se, Cd, Cr, V, Fe, and Mn, and between clay and Cd, Zn, V, Fe and Mn. Once again, these facts confirm the role of SOM and clay minerals in soil functions and that soil is an ecosystem element responsible for maintaining environmental quality.     

Heavy metal concentrations in roadside-deposited sediments in Kuwait city

In the present study, roadside-deposited sediment samples collected from Kuwait city district, in Kuwait, were analyzed for specific heavy metals (As, Cr, Cu, Mn, Ni, Pb, and Zn). Contamination assessment status of heavy metals in roadside sediments was made using mathematical models in terms of enrichment factor (EF), geoaccumulation index (I _geo), and contamination factor (CF). The sediments showed remarkably high levels of all the metals, except Ni, above background concentrations in the following order (As, Cu, Pb, Zn, Mn, and Cr). CF and I _geo revealed overall moderately uncontaminated and moderate contamination, respectively, but the EFs for all metals ranged between moderate and significant enrichment.     

Geochemical and statistical analysis of trace metals in atmospheric particulates in Wuhan, central China

The geochemical characteristics of trace metals (As, Cr, Co, Cd, Cu, Mn, Ni, Pb, V and Zn) in PM10 in Wuhan, the biggest metropolitan in central China, as well as their sources and contributions were analyzed. As PM10 has been the principal contaminant of air in Wuhan for years, concentrations of trace metals were measured in PM10 using high-volume samplers at one urban (Hankou) and one industrial (Changqian) site in Wuhan between September 2003 and September 2004. Based on the results, PM10 in Wuhan is characterized by relatively high levels of As, Cd, Mn, Pb and Zn compared with other Asian cities. The time-series of these elements indicated that As, Cu and Zn at both sites have similar trends, whereas Pb levels showed different patterns due to different emission sources. Factor analysis was applied to the datasets focusing on the apportionment of the mass of selected trace metals. Results indicate that Pb, Cd and As have a common source (smelting) at both sites, whereas the sources of Ni vary from coal combustion and steel in Changqian to mineral and traffic in Hankou.     

Distribution,fractionation, and contamination assessment of heavy metals in offshore surface sediments from western Xiamen Bay,China

Surface sediment samples were collected at 21 offshore sites in western Xiamen Bay, Southeast China. Total concentrations of Li, V, Cr, Co, Ni, Cu, Zn, Sr, Mn, Pb, Ba, Fe, and Ti were determined by inductively coupled plasma-optical emission spectrometry; Hg was determined by atomic fluorescence spectrometry. A modified BCR sequential extraction procedure was used to extract fractions of the above elements. Concentrations of Pb, Cr, and Hg at most sites met the primary standard criteria of Marine Sediment Quality except site S12 for Pb and S7 for Cr, while concentrations of Zn at 17 sites and Cu at seven sites exceeded the criteria. The mean concentration of Hg was three times higher than the background, with a possible source being the Jiulong River. Fe, Ti, Ba, Co, V, and Li dominated the residual phase, mainly from terrestrial input. Ni, Cr, Pb, and Hg in the non-residual phase varied largely between sites. Sr, Mn, Cu, and Zn were mainly in the non-residual fraction. Most sites showed considerable ecological risk; exceptions were site S7 (very high) and sites S10, S11, and S14 (moderate). Cu showed moderate-to-high pollution and Pb exhibited no-to-low pollution, while other metals had a non-pollution status according to their ratios of secondary phase to primary phase (RSP). Results of two assessment methods showed moderate pollution and a very high ecological risk for Cu, Zn, Ni, and Cr at site S7, which might be due to the local sewage treatment plant.     

Spatial distribution and contamination assessment of heavy metals in urban topsoil from inside the Xi’an second ringroad, NW China

The paper reports the spatial distribution and contamination level of heavy metals (Co, Cr, Cu, Mn, Ni, Pb, Zn and V) in urban topsoil from the interior area of the second ringroad of Xi’an city, China, based on X-ray fluorescence spectroscopy measurements. Geostatistical analysis shows that Co, Cu, and Pb have similar spatial distribution patterns. Heavy traffic density mainly contributed to the high concentrations of Co, Cu and Pb. The spatial distribution of Cr coincides with the industrial activity, whereas the spatial distribution of Zn differs from other heavy metals. The high concentrations of Zn coincide with heavy traffic and high population density. For Mn, Ni and V, natural factors are important in controlling their distribution. The calculated geoaccumulation indices indicate that urban topsoil inside the Xi’an second ringroad was uncontaminated by Cr, V, Mn and Ni, while Pb, Cu, Co and Zn are classified as uncontaminated to moderately contaminated with means of 0.64, 0.46, 0.26 and 0.21, respectively. The Nemero synthesis pollution index of these heavy metals revealed that the topsoil inside Xi’an second ringroad has been heavily contaminated due to anthropogenic activity.     

甘肃北山金、铜矿床红沙的植物地球化学特征及其找矿意义

北山地区植被属戈壁荒漠植被类型，主要植物群落为红沙，红沙中多数元素特别是成矿元素及其伴生元素的含量和变化系数矿区大于背景区，元素含量背景区呈对数正态分布，矿区呈偏对数正态或多峰分布，红沙中的元素组合分类背景区为Au,Cu,Pb,Zn,As,Sb,Mo,V,Mn和Ag,Sn,Sr,Ba及Ti,Cr,Co,Ni,金矿区为Au,Ag,As,Sb,Mo,Mn,Sr和Cu,Pb,Zn,Sn,Ba及Co,Ni,Ti,V,Cr,铜矿区为Cu,Pb,Zn,Mo,Au,Ag,Ba和As,Sb,Sn,Mn及Ti,V,Cr,Co,Ni,Sr，矿区红沙中浓集系数较大的元素多数在矿区岩石中的浓集系统亦较大，金，铜矿床红沙和岩石中的特征元素分别都有Au,Ag,Ag,Sb,Mo,(Mn)和Cu,Pb,(Ba,Ti,Cr)。在金，铜矿床（体上方分别发育有良好的Au和Cu的生物地球化学异常和元素组合及分带，根据红沙的地球化学特征能，判断金或铜矿种类型，并能对掩埋，隐伏金，铜矿床（体）进行定位预测。     

Nitric-acid soluble fractions of 21 elements in Norwegian podzols: Factors affecting regional differences in vertical distribution

Distributions of 21 major and trace elements in HNO₃ extracts of different horizons were studied in 13 podzol profiles from the boreal forest in different parts of Norway using ICP–MS. On the basis of ratios between the HNO₃-extractable fractions in the various horizons some general trends were elucidated. Two different groups of elements concentrated in the humus layer relative to the mineral horizons were identified, one mainly associated with contributions from air pollution (As, Cd, Sb, Pb), another one with plant nutrient circulation (K, Ca, Mn and to a lesser extent Mg, Co, Ni, Rb) and some with both mechanisms (Cu, Zn, Tl). The elements most clearly enriched along with Fe in the B horizon were V, Pb, Al, and Cr in that order, Pb partly because of leaching from the polluted organic surface soil. Four soils in the far south showed a behaviour distinctly different from the rest and were treated as a separate group. Relative to the more northerly sites the surface horizons of these soils were strongly depleted in lithogenic elements (Mg, Al, K, Ca, Sc, V, Cr, Mn, Fe, Co, La) and enriched in elements typical of long-range transport of pollutants (As, Cd, Sb, Tl, Pb). Also the B horizon in the southern soils was strongly depleted in the lithogenic group elements, including Fe and the associated metals. The main reason for this difference is assumed to be the greater influence of transboundary air pollution and associated metals and stronger soil acidification in the far south of the country.     

Spatial distribution, source identification and affecting factors of heavy metals contamination in urban–suburban soils of Lishui city, China

An investigation on spatial distribution, possible pollution sources, and affecting factors of heavy metals in the urban–suburban soils of Lishui city (China) was conducted using geographic information system (GIS) technique and multivariate statistics. The results indicated that the topsoils in urban and suburban areas were enriched with metals, such as Cd, Cu, Pb, and Zn. Spatial distribution maps of heavy metal contents, based on geostatistical analysis and GIS mapping, indicated that Cd, Cr, Cu, Mn, Ni, Pb, and Zn had similar patterns of spatial distribution. Their hot-spot areas were mainly concentrated in the densely populated old urban area of the city. Multivariate statistical analysis (correlation analysis, principal component analysis, and clustering analysis) showed distinctly different associations among the studied metals, suggesting that Cr, Cu, Ni, Pb, Cd, and Zn had anthropogenic sources, whereas Co and V were associated with parent materials and therefore had natural sources. The Cd, Cr, Ni, Pb, and Zn contents were positively correlated with soil organic matter, pH, and sand content (p < 0.01). It is concluded that GIS and multivariate statistical methods can be used to identify hot-spot areas and potential sources of heavy metals, and assess soil environment quality in urban–suburban areas.     

Metal contamination of the environment by placer and primary gold mining in the Adola region of southern Ethiopia

Primary and placer gold mining sites in southern Ethiopia were studied to see the contribution of mining to the accumulation of metals in different environmental media. Sediment, water and plant samples were analyzed for Al, Mn, Fe, As, Ni, Cr, Cu, Co, Pb, W, Sb, Mo, Zn and V. Water parameters (pH, Eh, TDS, anions and cations) were also measured. The sediment analyses results show that the most abundant metals are Ni (average 224.7 mg/kg), Cr (199 mg/kg), Cu (174.2 mg/kg), V (167.3 mg/kg), Zn (105.5 mg/kg), Pb (61.5 mg/kg) and As (59.7 mg/kg) in the primary gold mining sites while the placer sites show high concentration of V (average 301.2 mg/kg), Cr (260.4 mg/kg), Zn (179 mg/kg), Ni (113.4 mg/kg), Cu (46.7 mg/kg), As (32.2 mg/kg) and Co (31 mg/kg). The metals Cu, Ni, W, Cr, As and Pb in primary and Sb, W, Cr, Ni, Zn, As and Mo in placer gold mining sites have geoaccumulation indexes (I _geo) from one to four indicating considerable accumulation of these metals. Waters from both primary and placer mining sites are near neutral to alkaline. Arsenic (average 92.8 μg/l), Ni (276.6 μg/l), Pb (18.7 μg/l), Sb (10.7 μg/l), Mn (1 mg/l), Fe (8.3 mg/l) and Al (23.8 mg/l) exceeded the guideline value for drinking water. Plants show high concentration of Cr (average 174.5 mg/kg), Ni (163.5 mg/kg), Zn (96 mg/kg) and W (48 mg/kg). Zinc, W, Mo, Ni and Cr show the maximum biological absorption coefficient (BAC) ranging 0.4–1.7, 0.1–104.6, 1.1–2.6, 0.2–1.6 and 0.2–3.6, respectively, and the results suggest bioaccumulation of these elements in plants. The minerals especially sulfides in the ore aggregate are the ultimate source of the metals. The release of the metals into the environmental media is facilitated (in addition to normal geologic processes) by human activities related to gold mining.     

固体聚合膜电解浓集法测量天然水中低含量氚的化学淬灭效应研究

固体聚合膜电解浓集法是浓缩氚含量较低(1 Bq/m~3)的天然水样的常用方法,但因水样自身含有杂质离子或电解装置聚合膜带入杂质进入浓集液,使浓集液偏酸性,在测量过程中易产生化学淬灭效应,导致氚的测量值偏低。本文研究了水样自身存在的杂质离子和聚合膜上残留的杂质离子、样品溶液的pH值及其电导率所产生的化学淬灭效应的影响,实验表明,为减少化学淬灭效应,提高测量低含量氚的准确性,需保证水样溶液呈中性,电导率≤1μS/cm,同时避免杂质沉积在聚合膜上。如果水样溶液的pH值偏酸性、电导率大于1μS/cm,可采用酸碱混合型离子交换树脂去除水样中自身的杂质;对于聚合膜引入的杂质,可在电解后的水样中加入微量氨水将其pH值调节至中性。     

A 2400-year record of trace metal loading in lake sediments of Lagoa Vermelha, southeastern Brazil

Sediments of the Lagoa Vermelha (Red Lake), situated in the Ribeira Valley, southeastern Brazil, are made of a homogeneous, organic-rich, black clay with no visible sedimentary structures. The inorganic geochemical record (Al, As, Ba, Br, Co,Cs, Cr, Fe, Mn, Ni, Rb, Sc, Sb, V, Zn, Hg and Pb) of the lake sediments was analyzed in a core spanning 2430 years. The largest temporal changes in trace metal contents occurred approximately within the last 180 years. Recent sediments were found to be enriched in Pb, Zn, Hg, Ni, Mn, Br and Sb (more than 2-fold increase with respect to the “natural background level”). The enhanced accumulation of Br, Sb, and Mn was attributed to biogeochemical processes and diagenesis. On the other hand, the anomalous concentrations of Pb, Zn, Hg and Ni were attributed to pollution. As Lagoa Vermelha is located in a relatively pristine area, far removed from direct contamination sources, the increased metal contents of surface sediments most likely resulted from atmospheric fallout. Stable Pb isotopes provided additional evidence for anthropogenic contamination. The shift of ²⁰⁶Pb/²⁰⁷Pb ratios toward decreasing values in the increasingly younger sediments is consistent with an increasing contribution of airborne anthropogenic lead. In the uppermost sediments (0-10 cm), the lowest values of the ²⁰⁶Pb/²⁰⁷Pb ratios may reflect the influence of the less radiogenic Pb from the Ribeira Valley District ores (²⁰⁶Pb/²⁰⁷Pb between 1.04 and 1.10), emitted during the last 50 years.     

Use of measurement uncertainty in a probabilistic scheme to assess compliance of bottled water with drinking water standards

Ground water bodies are important resources for drinking water, including bottled water, and national regulatory bodies should assess their quality continuously. For this purpose, an effective assessment system of bottled water at source should be installed. A hierarchical nested balance design for the collection of random primary duplicate water samples, and their replicate analyses, is described, and the use of robust analysis of variance to estimate measurement uncertainty. The latter is subsequently used for the development of four probabilistic categories for the classification of element concentrations in bottled water with respect to legislative standard values, i.e., (a) compliant (below Lower Threshold Limit), (b) possibly non-compliant (possibly above Standard Value), (c) probably non-compliant (probably above Standard Value), and (d) non-compliant (above Upper Threshold Limit), for the reliable assessment of compliance to European Union and national drinking water standards. Overall, the quality of European bottled water is considered good, with the exception of a few that have concentrations in Mn, B, Ba, As, Fe, Ni, Se, and Al, which are definitely above the estimated respective Upper Threshold Limit and, thus, exceed the corresponding legislative standard value defined by European Union directives. National regulatory bodies should verify these results, and install an efficient assessment system of compliance to regulatory limits using the methodology described in this paper.     

Geochemical assessment and speciation of metals in sediments of Osun and Erinle Rivers,Southwestern Nigeria

Fifty sediment samples were collected from Osun (urban) and Erinle (suburban) rivers in addition to ten samples of the underlying rock types (schist and gneiss) and analyzed for elemental constituents while speciation of metals was determined by sequential analysis. Data were geochemically evaluated and ArcGIS was used to generate geochemical maps. Metal concentrations (ppm) in sub-urban and urban areas were Cd (0.2–0.2, 0.2–1.1), Cu (37.0–272.0, 49.0–970.0), Ni (6.0–27.0, 3.0–43.0), Pb (16.0–67.0, 15.0–2650.0), Zn (32.0–170.0, 50.0–987.0), Co (8.0–60.0, 2.0–86.0), Cr (26.0–153.0, 9.0–128.0), V (30.0–142.0, 9.0–135.0), and Mn (442.0–5100.0, 107.0–3930.0), respectively. In the rocks, Cu, Ni, Pb, Co, Cr, V, and Zn, concentrations (ppm) were below detection limit (BDL)-0.05, BDL-38.00; 6.23–12.00, BDL-20.00; 3.78–6.23, BDL-5.00; BDL-0.20, BDL-4.00; 5.00–9.00, BDL-66.00; 15.99–32.00, BDL-130.00; and 18.00–26.00, BDL-48.00, respectively, with Cu, Pb, Zn, Cd, and Mn of elevated concentrations in sediments compared with that of the rocks, being indication of additional anthropogenic sourcing. Calculated contamination indices revealed contamination for sediment from the urban areas compared to those from the sub-urban. High percentage of Pb (2.94–81.92%), Cu (31.69–45.95%), Zn (49.2–65.5%), Cd (31.69–45.95%), and Mn (12.13–37.50%) are hosted by the bio-available phases (carbonate, organic, and sulfide). The geochemical distribution of metals in the sediments of the Osun and Erinle rivers is governed by both geogenic (Ni-Cr-Co-V) and anthropogenic (Pb-Cd-Zn) activities. Elevated concentration and occurrences of the selected metals in the bio-available phases pose potential health risk to people in the urban area.     

Geostatistical analyses and fractionation of heavy metals in urban soil from industrial district in Weinan, NW China

The concentrations of metals (Pb, Cr, Ba, Zn, V, Mn, Co, Cu, Ni and As) in 38 soil samples collected from the industrial district in Weinan (NW China) were determined by wavelength dispersive X-ray fluorescence spectrometry. The magnetic parameters of soil including low-/high-frequency susceptibility and frequency-dependent susceptibility were measured. The modified three-step BCR sequential extraction procedure was used to evaluate mobility, availability and persistence of trace elements in urban soil samples. Multivariate (principal component analysis, clustering analysis and correlation analysis) and geostatistical analysis (ArcGIS tools) were applied to the obtained data to evaluate the analytical results and to identify the possible pollution sources of metals as well as geo-spatial distributions. The results revealed that the sampling area was mainly influenced by two main sources: (1) Ba, Cu, Pb, Cr and Zn were mainly derived from industrial sources, which combined with coal combustion as well as traffic factor. The mobility sequence based on the sum of the BCR sequential extraction stages was: Pb (53.79 %) > Zn (51.78 %) > Cu (50.96 %) > Ba (42.59 %) > Cr (18.47 %). Pb was the metal predominantly associated (~46.86 %) with the form bound to Fe/Mn oxides, and the highest percentage of Zn was exchangeable and carbonate-bound fraction. Cu was present mainly in organic fraction, while the residual fraction was the most dominant solid phase pool of Cr (~81.53 %) and Ba (~57.41 %). (2) Mn, V, Co, As and Ni in the study area were consistently from natural sources. The analysis of enrichment factors indicated that urban soils in Weinan City were classified as having significant enrichment by Ba, Cu, Pb, Cr and Zn. The overall results proposed the future tactics for Weinan environment quality control on a local scale that concerned not only the levels of risky, but also the industrial emission abatement techniques as well as urban setting.     

Hydrological and geochemical control of metals and arsenic in a Mediterranean river contaminated by acid mine drainage (the Amous River,France); preliminary assessment of impacts on fish (Leuciscus cephalus)

Dissolved and particulate concentrations of metals (Fe, Al, Mn, Co, Ni, Cu, Zn, Cd, Tl, Pb) and As were monitored over a 5 year period in the Amous River downstream of its confluence with a creek severely affected by acid mine drainage (AMD) originating from a former Pb–Zn mine. Water pH ranged from 6.5 to 8.8. Metals were predominantly in dissolved form, except Fe and Pb, which were in particulate form. In the particulate phase, metals were generally associated with Al oxides, whereas As was linked to Fe oxides. Metal concentrations in the dissolved and/or particulate phase were generally higher during the wet season due to higher generation of AMD. Average dissolved (size < 0.22 μm) metal concentrations (μg/L) were 1 ± 4 (Fe), 69 ± 49 (Al), 140 ± 118 (Mn), 4 ± 3 Co, 6 ± 4 (Ni), 1.3 ± 0.8 (Cu), 126 ± 81 (Zn), 1.1 ± 0.7 (Cd), 0.9 ± 0.5 (Tl), 2 ± 3 (Pb). Dissolved As concentrations ranged from 5 to 134 μg/L (30 ± 23 μg/L). During the survey, the concentration of colloidal metals (5 kDa < size < 0.22 μm) was less than 25% of dissolved concentrations. Dissolved metal concentrations were generally higher than the maximum concentrations allowed in European surface waters for priority substances (Ni, Cd and Pb) and higher than the environmental quality standards for other compounds. Using Diffusion Gradient in Thin Film (DGT) probes, metals were shown to be in potentially bioavailable form. The concentrations in Leuciscus cephalus were below the maximum Pb and Cd concentrations allowed in fish muscle for human consumption by the European Water Directive. Amongst the elements studied, only As, Pb and Tl were shown to bioaccumulate in liver tissue (As, Pb) or otoliths (Tl). Bioaccumulation of metals or As was not detected in muscle.     

Modeling the composition of mine (Waste Rock) water at the deposits of the Balkhach gold-bearing field

Modeling of hydrogeochemical processes in the rock-water system showed that the concentrations of Al, Fe, Sb, Sr, and W do not exceed the MAC levels even under conditions of prolonged interaction between water and rock minerals (R/W > 0.0001). The concentrations of As, Cd, Co, and Se are unlikely to significantly exceed the MAC even at decreasing rates of water exchange (at increasing R/W) owing to the low concentrations of these elements in the rocks of the deposit. The concentrations of Mn are likely to exceed the MAC level under reducing conditions, while they remain well within the MAC under weakly to moderately oxidizing conditions. A different situation is for Cr and S, which may be well above the MAC under oxidizing conditions and below the MAC under reducing conditions, when weakly oxidized species of S and Cr predominate. Model and measured concentrations of Cu, Mo, Ni, Pb, V, and Zn are generally similar to each other and to the MAC levels, but they may considerably exceed the MAC in the case of reduction in water exchange rates (longer duration of water-rock interaction and higher R/W). The concentrations of Cu, Mo, Ni, Pb, V, Zn, and Cr may exceed the MAC levels in the case of the prolonged exposure of strongly disintegrated rocks to moist air, whereas the wet environment is favorable for Mn hydroxide precipitation.