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1.
The River Vişeu catchment in Maramureş County, northwestern Romania, has a long history of base and precious metal mining. Between 1994 and 2003 waste from mining activity at Baia Borşa was stored in the Novaţ-Roşu tailings pond in the upper Vişeu catchment. However, in March 2000, the tailings dam failed releasing approximately 100,000 m3 of contaminated water and 20,000 t of mineral-rich solid waste, which was routed downstream through the Rivers Novaţ, Vaser and Vişeu into the River Tisa. Following the accident metal (Cd, Cu, Pb, Zn) concentrations in river water and river channel sediment were assessed in samples collected annually (July 2000, 2001, 2002 and 2003) from 29 sites in the Vişeu catchment, downstream of the tailings pond. Additionally, the speciation of sediment-associated metals was established using a 4-stage sequential extraction procedure (SEP) and Pb isotope analysis (206/204Pb and 207/204Pb) was carried out to establish the provenance of contaminated sediments. Metal concentrations in river water were found to comply with EU directive ‘target’ values within four months of the failure. However, the impact of the spill upon river channel sediments was found to be much longer-lasting, with evidence of the delayed downstream remobilization of tailings stored within the narrow Novaţ valley following the dam failure, as well as continued inputs of contaminated sediment to the River Vişeu from the River Tisla, another mining-affected tributary. Comparison with data from other recent tailings dam failures, indicates that river system recovery rates depend upon local geomorphological conditions, hydrological regimes, and the nature and scale of post-spill clean-up operations.  相似文献   

2.
Total concentrations of 13 elements (K, Ca, Ti, Cr, Mn, Fe, Cu, Zn, Rb, Sr, Y, Zr, Pb) in the size-fractionated Sava River sediments upstream and downstream of the Krsko nuclear power plant together with metal speciation within bulk sediment have been investigated. Trace metals generally increase with decreasing particle size, however, because of entrapment of organic matter in the 0.63–1 mm fraction, concentrations in the coarser sediment fraction are higher than expected. Exchangeable Pb, Zn, Cu, Mn, Cr and Fe are generally found to represent a negligible fraction of the total metal concentration of the bulk sediment. Seasonal variations of the Pb, Zn and Cu concentrations in the <0.5 mm fraction reflect decreased values during the spring period. Heavy metal concentrations in the 2003 waste water discharges from the Krsko nuclear power plant released into the Sava River were much lower than their maximum allowed values. Combined rubidium and organic matter normalization of the Zn, Pb and Cu concentrations, which was applied on the minus 0.063 mm fraction, indicated three potential sources of contaminants.  相似文献   

3.
Rivers in metropolitan areas are often highly polluted with materials that pose a threat to a large number of residents. Human influences lead to contaminants in metropolitan rivers having more complex sources than those in rural rivers. This complexity results in contamination that is unstable and rapidly changing. Here, the contents and chemical fractionation patterns of eleven toxic elements (As, Cd, Co, Cu, Cr, Mn, Ni, Pb, Zn, Y, and Hg) were evaluated in 13 samples collected from along the Beiyunhe River in Beijing, China. The results revealed that the metal contents were unevenly distributed along the river, with higher levels being observed in the downriver sites and the rendezvous sites. Additionally, more than 80% of the metals were found to be in the residual phase. The organic and sulfide phases were the most important extractable phases of most metals, with Ni, Co, Cu, and Cr primarily being associated with these phases and As, Cd, and Zn having a strong association with the iron/manganese oxide and hydroxide phases. Additionally, Mn was associated with the exchangeable and carbonate phases, with the lowest concentrations being observed in the organic and sulfide phases. Conversely, the metal exchangeable and carbonate phases were uniformly distributed throughout the river. Analysis of the metal sources revealed that particles input from the atmosphere comprised a considerable amount of the metals in the Beiyunhe River. However, these metals likely do not enter the sediment via atmospheric deposition directly, but rather through rainwater runoff into the river. The methods used in the present study will be useful in other studies that require analysis of complex data.  相似文献   

4.
Soils from historical Pb mining and smelting areas in Derbyshire, England have been analysed by a 5-step sequential extraction procedure, with multielement determination on extraction solutions at each step by ICP-AES. Each of the chemical fractions is operationally defined as: (i) exchangeable; (ii) bound to carbonates or specifically adsorbed; (iii) bound to Fe–Mn oxides; (iv) bound to organic matter and sulphides; (v) residual. The precision was estimated to be about 5%, and the overall recovery rates were between 85 and 110%. The carbonate/specifically adsorbed and Fe–Mn oxide phases are the largest fractions for Pb in soils contaminated by both mining and smelting. Most of the Zn is associated with Fe–Mn oxide and the residual fractions. Cadmium is concentrated in the first 3 extraction steps, particularly in the exchangeable phase. The most marked difference found between soils from the mining and smelting sites is the much higher concentrations and proportions of metals in the exchangeable fraction at the latter sites. This indicates greater mobility and potential bioavailability of Pb, Zn and Cd in soils at the smelting sites than in those in the mining area. The most important fraction for Fe and Al is the residual phase, followed by the Fe–Mn oxide forms. In contrast, the Fe–Mn oxide fraction is the dominant phase for Mn in these soils. In the mining area, most of the Ca is in the carbonate fraction (CaCO3), while the exchangeable and residual phases are the main fractions for Ca at the smelting sites. Phosphorus is mainly in the residual and organic fractions in both areas. The exchangeable fractions of Pb, Zn and Cd in soils were found to be significantly related to the concentrations of these metals in pasture herbage.  相似文献   

5.
Macquarie Harbour in southwest Tasmania, Australia, has been affected severely by the establishment of mines in nearby Queenstown in the 1890s. As well as heavy metal-laden acid rock drainage from the Mount Lyell mine area, over 100 Mt of mine tailings and slag were discharged into the Queen and Ring Rivers, with an estimated 10 Mt of mine tailings building a delta of ca. 2.5 km2 and ca. 10 Mt of fine tailings in the harbour beyond the delta. Coring of sediments throughout Macquarie Harbour indicated that mine tailings accreted most rapidly close to the King River delta source with a significant reduction in thickness of tailings and heavy metal contamination with increasing distance from the King River source. Close to the King River delta the mine tailings are readily discriminated from the background estuarine sediments on the basis of visual logging of the core (laminations, colour), sediment grain size, sediment magnetic susceptibility and elemental geochemistry, especially concentrations of the heavy metals Cu, Zn and Pb. The high heavy metal concentrations are demonstrated by the very high contamination factors (CF > 6) for Cu and Zn, with CF values mostly >50 for Cu for the mine-impacted sediments. Although the addition of mine waste into the King River catchment has ceased, the catchment continues to be a source of these heavy metals due to acid rock drainage and remobilisation of mine waste in storage in the river banks, river bed and delta. The addition of heavy metals to the harbour sourced from the Mount Lyell mines preceded the advent of direct tailings disposal into the Queen River in 1915 with the metals probably provided by acid rock drainage from the Mount Lyell mining area.  相似文献   

6.
A sediment core collected from coastal zone near the Qiao Island in the Pearl River Estuary was analyzed for total metal concentrations, chemical partitioning, and physico-chemical properties. Three vertical distribution patterns of the heavy metals in the sediment core were identified, respectively. The dominant binding phases for Cu, Pb, Cr, and Zn were the residual and Fe/Mn oxides fractions. Cd in all sediments was mainly associated with exchangeable fraction. Influences of total organic carbon content and cation exchange capacity on the total concentrations and fractions of almost all the metals were not evident, whereas sand content might play an important role in the distributions of residual phases of Cr, Cu, Pb, and Zn. In addition, sediment pH had also an important influence on the Fe/Mn oxides, organic/sulfide and residual fractions of Cr, Cu, and Zn. Contamination assessment on the heavy metals in the sediment core adopting Index of Geoaccumulation showed that Cr, V, Be, Se, Sn, and Tl were unpolluted, while Cu, Ni, Pb, Zn, Cd, and Co were polluted in different degrees throughout the core. It was remarkable that the various pollution levels of the metals from moderate (for Cu, Pb, and Zn) to strong (for Cd) were observed in the top 45 cm of the profiles. The relative decrease of the residual fraction in the upper 45 cm of the core is striking, especially for Zn and Cu, and, also for Pb, and Cr. The change in fraction distribution in the upper 45 cm, which is very much contrasting to the one at larger depths, confirms that the residual fraction is related to the natural origin of these metals, whereas in the upper part, the non-residual fractions (mainly the Fe/Mn oxides fraction) are increased due to pollution in the last decade. The possible sources for Cu, Pb, Zn, and Cd contaminations were attributed to the increasing municipal and industrial wastewater discharges, agricultural runoff, atmospheric inputs, and runoff from upstream mining or smelting activities, which may be associated with an accelerating growth of economy in the Pearl River Delta region in the past decade.  相似文献   

7.
A study of the San Pedro River (SPR), which is located in a semi-arid region in Sonora, Mexico, was conducted to evaluate the chemical, spatial and temporal (mobilization) trends of potentially harmful metals in its sediment in the rainy and dry seasons. High total concentrations of metals were detected in the following order: Fe > Cu > Mn > Zn > Pb > Cd. All studied metals except for Pb were increased during the dry season showing the effect of climate on the metal distribution in sediments. The results of sequential extraction indicated that the residual and Fe/Mn oxide fractions were the most important with regard to retaining potentially harmful metals in the sediments. In the exchangeable carbonate and Fe oxide fractions, high concentrations of metals were detected, representing high environmental risk. The geoaccumulation index shows slight to moderate contamination in most samples, and sampling point E4 (related to cattle activity) shows strong contamination for Cd, Cu, Pb and Zn. Enrichment factors (EFs) demonstrate anthropogenic origins for Pb (EF: 3–57), Cd (EF: 6–73) and Cu (EF: 1.5–224). This study shows that sediments are impacted by anthropogenic activities related to the mining industry, untreated wastewater discharges from the city of Cananea and cattle activities. Metal mobility in the SPR can disrupt the development of aquatic species in the river.  相似文献   

8.
The long-term industrialization and urbanization of Guangzhou city may lead to heavy metal contamination of its aquatic sediment. Nevertheless, only few studies have been published on the distribution and contamination assessment of heavy metals in this urban river sediment. Thus, the major objective of this study was to quantitatively assess contamination of heavy metals and their chemical partitioning in the sediments of the Guangzhou section of the Pearl River (GSPR). Surface sediment samples were collected at 10 sites in the main river and 12 sites in the creeks of the GSPR. The total content of Cd was determined by graphite furnace atomic adsorption spectrometry (GF-AAS), and content of Cr, Cu, Pb and Zn was determined by inductively coupled plasma atomic emission spectrometry (ICP-AES). The chemical partitioning of these heavy metals in the sediments of the main river was determined by the sequential selective extraction (SSE) method. Results indicated that the average total concentrations of Cd, Cr, Pb, Cu and Zn in the sediments of the main river were 1.44, 63.7, 95.5, 253.6 and 370.0 mg/kg, respectively, whereas they were 2.10, 125.5, 110.1, 433.7 and 401.9 mg/kg in the sediments of the creeks. The sediment at M4 and C9 sites was heavily contaminated with about 8 and 11 of toxic unit, respectively. Cr, Cu, Pb and Zn were mostly bound to organic matter and in the residual phase, whereas Cd was mostly associated with the soluble and exchangeable phase and the residual phase. The mobility and bioavailability of Cd, Zn and Cr in the sediments of the main river were relatively higher than Cu and Pb, due to higher levels in the soluble and exchangeable fraction and the carbonate fraction. The potential acute toxicity in the sediments of the main river and creeks was mainly caused by Cu contamination, accounting for 21.7–37.1% and 16.9–46.3% of the total toxicity, respectively, followed by Zn and Pb. Adverse biological effects induced by heavy metals would be expected in the sediments of the GSPR. Therefore, the sediments of the GSPR, especially at M4 and C9 sites, need to be remediated to maintain aquatic ecosystem health.  相似文献   

9.
 The Yamuna River sediments, collected from Delhi and Agra urban centres, were analysed for concentration and distribution of nine heavy metals by means of atomic adsorption spectrometry. Total metal contents varied in the following ranges (in mg/kg): Cr (157–817), Mn (515–1015), Fe (28,700–45,300), Co(11.7–28.4), Ni (40–538), Cu (40–1204), Zn (107–1974), Pb (22–856) and Cd (0.50–114.8). The degree of metal enrichment was compared with the average shale concentration and shows exceptionally high values for Cr, Ni, Cu, Zn, Pb and Cd in both urban centres. In the total heavy metal concentration, anthropogenic input contains 70% Cr, 74% Cu, 59% Zn, 46% Pb, 90% Cd in Delhi and 61% Cr, 23% Ni, 71% Cu, 72% Zn, 63% Pb, 94% Cd in Agra. A significant correlation was observed between increasing Cr, Ni, Zn, and Cu concentrations with increasing total sediment carbon and total sediment sulfur content. Based on the Müller's geoaccumulation index, the quality of the river sediments can be regarded as being moderately polluted to very highly polluted with Cr, Ni, Cu, Zn, Pb and Cd in the Delhi and Agra urban centres. The present sediment analysis, therefore, plays an important role in environmental measures for the Yamuna River and the planning of these city centres. Received: 21 June 1999 · Accepted: 1 October 1999  相似文献   

10.
The Rio Tinto in SW Spain drains Cu and pyrite mines which have been in operation since at least the Bronze Age. Extensive metal mining, especially from 1873 to 1954, has resulted in contamination of the Rio Tinto alluvium with As, Cu, Pb, Ag and Zn. X-ray diffraction (XRD), wavelength-dispersive X-ray mapping, scanning electron microscope petrography and X-ray energy-dispersive (EDX) analysis has revealed that 4 major groups of contaminant metal and As-bearing minerals, including sulphides, Fe-As oxides, Fe oxides/hydroxides/oxyhydroxides, and Fe oxyhydroxysulphates, occur in the alluvium. Sulphide minerals, including pyrite, chalcopyrite, arsenopyrite and sphalerite, occur in alluvium near the mining areas. Iron hydroxides and oxyhydroxides such as goethite and possibly ferrihydrite occur in cements in both the mining areas and alluvium downstream, and carry minor amounts of As, Cu and Zn. Iron oxyhydroxysulphates, including jarosite, plumbojarosite and possibly schwertmannite, are the most common minerals in alluvium downstream of the mining areas, and are major hosts of Cu, Pb, Zn and of As, next to the Fe-As minerals. This work, and other field observations, suggest that (1) the extreme acidity and elevated metal concentrations of the river water will probably be maintained for some time due to oxidation of pyrite and other sulphides in the alluvium and mine-waste tips, and from formation of secondary oxide and oxyhydroxysulphates; (2) soluble Fe oxyhydroxysulphates such as copiapite, which form on the alluvium, are a temporary store of contaminant metals, but are dissolved during periods of high rainfall or flooding, releasing contaminants to the aqueous system; (3) relatively insoluble Fe oxyhydroxysulphates and hydroxides such as jarosite and goethite may be the major long-term store of alluvial contaminant metals; and (4) raising river pH will probably cause precipitation of Fe oxyhydroxides and oxides/hydroxides/oxyhydroxides and thus have a positive effect on water quality, but this action may destabilise some of these contaminant metal-bearing minerals, releasing metals back to the aqueous system.  相似文献   

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