Trace metal composition and speciation in street sediment: Sault Ste. Marie,Canada

Street sediment collected in Sault Ste. Marie, Ontario was examined for trace element composition (As, Cd, Cr, Cu, Fe, Pb, Hg, Ni and Zn) and the metal partitioning to various sediment properties was determined by sequential extraction. Total Ni, Cu, Zn and Pb concentrations exceeded the lowest effect levels specified in the Ontario Provincial Sediment Quality Guidelines for Metals (Environment Ontario, 1992) and derived from bioassay studies. According to these Guidelines, the disposal of such sediment has to be guided by environmental considerations. A significant fraction of these metals was extractable in 0.5 N HCl over a 12-hour period and considered as potentially bioavailable. The major accumulative phases of toxic metals in this sediment are exchangeable, carbonate, Fe/Mn oxides and organic matter but the relative importance of each phase varied for individual metals. Approximately 20% of the total extractable Cd is found in each of these four fractions. Pb, Zn and Mn are predominantly bound to carbonates, Fe/Mn oxides and organic matter. Cu shows a high affinity for organic matter and to a lesser extent for carbonates. Elevated levels of Cd, Pb, Cu, Zn, Mn and Cr in the exchangeable and/or soluble phase suggest that sediment associated metals, mobilised from streets in Sault Ste. Marie during runoff and snowmelt, would adversely impact water quality in the receiving waters. However, large fractions of the total metal load are associated with coarser particles which are unlikely to be transported through the drainage system into receiving waters.     

Heavy Metal Fractionation and Extractability in Dredged Sediment Derived Surface Soils

The objective of this study was to characterise pollution with heavy metals in surface soils sampled at various dredged sediment disposal sites in the Flemish region (Belgium). The sites selected varied in the period since sediment disposal ceased and in current vegetation and land use. Total metal contents (Cd, Co, Cu, Fe, Mn, Ni, Pb, and Zn) in the surface soils varied widely. For some disposal sites Cd and Zn concentrations greatly exceeded reference values for clean soil. The distribution of the metals as determined by sequential extraction differed between elements, but was simular for all the soils. This suggested that metals in these sediment derived surface soils were accumulated and transformed in a similar way. Residual fractions were low compared to total contents (2 – 4% for Cd, 25% – 35% for Co, 7 – 18% for Mn, 4 – 22% for Zn, 12 – 41% for Ni, 11 – 42% for Pb, 20 – 45% for Cu, < 10% for Zn). High metal concentrations in the acid-extractable and reducible fractions may indicate pollution from anthropogenic sources. DTPA-extractable metals, which may be considered indicative of plant-available contents, were relatively high compared to the total contents. The relative extractability, expressed as the ratio of DTPA-extractable to total contents, decreased in the order Cd (38%) > Cu (28%) = Zn (26%) > Pb (13%) > Ni (10%) > Co (3%). Most of the sites studied would be of concern if they were used for agricultural activities. No trends in metal availability in the period following disposal were apparent from the data.     

滇池内湖滨带重金属污染及其生态风险评价

水体沉积物是重金属元素的重要载体,其含量高低能反映水环境质量现状。采集滇池内湖滨带沉积物样品,分析了滇池内湖滨带表层沉积物中Pb、Cd、Cu、Zn、Cr、Ni、Fe、Mn 8种重金属元素含量特征,并用Hakanson潜在生态危害指数法评价其生态危害,旨在为合理预防和治理滇池内湖滨带的重金属污染以及内湖滨带生态系统的修复提供基础资料。结果表明,与“全国土壤环境质量标准”对比,表层沉积物中主要是Cd、Cu、Zn超标,重金属污染强度总体上是草海＞外海。不同重金属间的相关性分析结果表明,Cu-Cd之间呈极显著相关,说明这两种元素污染源可能相同,几种污染重金属与胶体矿物元素Fe、Mn间的相关性不大,说明在所调查沉积物中,Fe/Mn氧化物或氢氧化物共沉淀或吸附Pb、Cd、Cu、Zn、Cr、Ni元素量较少。由潜在生态风险评价结果可知,滇池内湖滨带表层沉积物已具极强生态危害,各重金属对滇池内湖滨带生态风险影响程度由高到低依次为：Cd〉Cu〉Pb〉Ni〉Zn≈Cr。     

Road-deposited sediment, soil and precipitation (RDS) in Bratislava, Slovakia: compositional and spatial assessment of contamination

Background, aim and scope  The urban environment in Bratislava is, in association with rapid urbanisation and industrialisation, significantly influenced by several potential sources of pollution, including automobile exhaust and industry emmissions. Urban road-deposited sediments contain many potentially toxic elements such as Pb, Cr, Cu, Zn and also Fe at concentrations much higher than in soil. In this study, the chemical composition and spatial variability of road-deposited sediments in urban area of Bratislava were assessed for the elements As, Cd, Cr, Cu, Hg, Ni, Pb, Fe and Mn. Additional evaluation of archive data for soil, snow and atmospheric dust was undertaken to provide an integrated view on urban environment contamination. Materials and methods  Urban road-deposited sediments (RDS) were collected during summer 2003 and 2004 mainly from major city crossroads. RDS samples were analysed for total metal content, pseudo-total metal content (HNO₃ digestion) and by a sequential extraction method, grain fraction composition and mineralogical composition (X-ray analysis). Metal concentrations in soil and snow samples from urban and non urban city area were compared. Results and discussion  The highest concentrations for all metals were found in the finest RDS fraction (<0.125 mm). Whilst in the fraction <1 mm mean concentrations of Cr, Cu and Pb reached 55.2, 143.8 and 34.4 mg kg⁻¹, respectively, for the fraction <0.125 mm, markedly higher contents of these elements were documented at the level of 86.8, 218.4 and 63.1 mg kg⁻¹, respectively. The soil contents of potentially toxic risk elements in the urban area including As, Cr, Cu, Fe, Hg, Mn, Ni, Pb and Zn were higher than in the non-urban area (except for Cd with similar contents). This distribution pattern of evaluated chemicals in urban and non-urban area is more evident in the case of winter precipitation (snow). The snow concentrations of As, Cr, Cu, Fe, Mn, Pb and Zn in the urban area were two tot five times higher than in non-urban area. Conclusions and recommendations  Monitoring of road-deposited sediments, dust, soil and precipitation has confirmed the significant contamination of the urban environment in Bratislava with potentially toxic elements that can pose a threat for the health of its residents. Future works should be based on analyses of temporal variability of RDS and analyses of organic matter content.     

Incidence of heavy metals in street surface sediments: Solubility and grain size studies

Samples of surface and gutter sediment from roads within N.W. London have been analyzed for levels of Cd, Cu, Fe, Mn, Pb, and Zn. Sediment and associated metal grading curves are presented and apart from Mn and Fe which reflect natural background levels, the remaining metals show distributions which relate to road type and traffic conditions. For highways carrying the highest traffic densities the concentrations of Cd and Pb are greatest for grain sizes between 100 and 500 µm and an aggregation process is postulated. Residential side street samples show a marked affinity of Cd, Fe, and Zn for the coarsest grain fractions. Laboratory sorption and desorption studies are described and solution concentrations are obtained for Cd, Cu, Mn, Pb, and Zn over 1 to 30 day time periods. Solubility curves are typically variable with time. The relationship of leachate patterns to particle size and sample site location is discussed and its relative importance to Stormwater loadings is considered. Extraction efficiencies for the five metals are found to be independent of road type and in the order Cd > Zn, Cu > Mn > Pb. The relevance of this hierarchy to Stormwater toxicity is discussed.     

Heavy Metals in Freshly Deposited Stream Sediments of Rivers Associated with Urbanisation of the Ganga Plain,India

Freshly deposited stream sediments from six urban centres of the Ganga Plain were collected and analysed for heavy metals to obtain a general scenery of sediment quality. The concentrations of heavy metals varied within a wide range for Cr (115–817), Mn (440–1 750), Fe (28 700–61 100), Co (11.7–29.0), Ni (35–538), Cu (33–1 204), Zn (90–1 974), Pb (14–856) and Cd (0.14–114.8) in mg kg^-1. Metal enrichment factors for the stream sediments were <1.5 for Mn, Fe and Co; 1.5–4.1 for Cr, Ni, Cu, Zn and Pb; and 34 for Cd. The anthropogenic source in metals concentrations contributes to 59% Cr, 49% Cu, 52% Zn, 51% Pb and 77% Cd. High positive correlation between concentrations of Cr/Ni, Cr/Cu, Cr/Zn, Ni/Zn, Ni/Cu, Cu/Zn, Cu/Cd, Cu/Pb, Fe/Co, Mn/Co, Zn/Cd, Zn/Pb and Cd/Pb indicate either their common urban origin or their common sink in the stream sediments. The binding capacity of selected metals to sediment carbon and sulphur decreases in order of Zn > Cu > Cr > Ni and Cu > Zn > Cr > Ni, respectively. Stream sediments from Lucknow, Kanpur, Delhi and Agra urban centres have been classified by the proposed Sediment Pollution Index as highly polluted to dangerous sediments. Heavy metal analysis in the <20-μm-fraction of stream sediments appears to be an adequate method for the environmental assessment of urbanisation activities on alluvial rivers. The present study reveals that urban centres act as sources of Cr, Ni, Cu, Zn, Pb and Cd and cause metallic sediment pollution in rivers of the Ganga Plain.     

Enhanced Heavy Metal Phytoextraction from Marine Dredged Sediments Comparing Conventional Chelating Agents (Citric Acid and EDTA) with Humic Substances

Metal (Cu, Mn, Ni, Zn, Fe) concentrations in marine sediment and zooplankton were investigated in Izmir Bay of the Eastern Aegean Sea, Turkey. The study aimed to assess the levels of metal in different environmental compartments of the Izmir Bay. Metal concentrations in the sediment (dry weight) ranged between 4.26–70.8 μg g^?1 for Cu, 233–923 μg g^?1 for Mn, 14.9–127 μg g^?1 for Ni, 25.6–295 μg g^?1 for Zn, 12,404–76,899 μg g^?1 for Fe and 38,226–91,532 μg g^?1 for Al in the Izmir Bay. Maximum metal concentrations in zooplankton were observed during summer season in the inner bay. Significant relationships existed between the concentrations of certain metals (Al, Fe, Mn and Ni) in sediment, suggesting similar sources and/or similar geochemical processes controlling such metals. Higher concentrations of Cu, Zn and percent organic matter contents were found in the middle-inner bays sediments. Based on the correlation matrix obtained for metal data, organic matter was found to be the dominant factor controlling Cu and Zn distributions in the sediment. In general, mean Cu and Zn levels in the bay were above background concentrations in Mediterranean sediments. Zooplankton metal concentrations were similar to sediment distributions.     

Assessment of Fe,Zn, Cd,Hg, and Pb in the Jordan and Yarmouk River Sediments in Relation to Their Physicochemical Properties and Sequential Extraction Characterization

Forty-six surface sediment samples taken along the beds of boththe Jordan and Yarmouk Rivers were analysed for Pb, Cd, Zn, Fe andHg by atomic absorption spectrophotometer. Extraction techniqueswere used to establish the association of the total concentrations of Pb, Cd, Zn and Fe in the sediment samples withtheir contents in the exchangeable, carbonate, Fe/Mn oxides, organic and residual fractions.In the sediments of the Jordan River the recorded heavy metalsconcentrations were as follow: 8.1 ppm for Pb, 0.63 ppm for Cd, 20.3 ppm for Zn, 6 ppm for Hg and 1265.6 ppm for Fe; whereas in the sediment of Yarmouk River were 8.4 ppm for Pb, 0.67 ppm for Cd, 26.4 ppm for Zn, 6.2 ppm for Hg and 1370 ppmfor Fe. Pb, Cd, Zn, and Fe concentrations in the sediments ofboth rivers reflect the natural background value in shale, whereas Hg is moderately enriched. I-geo (geo-accumulation index) of metals in the sediments under study indicates thatthey are uncontaminated with Pb, Zn and Fe; contaminated tomoderately contaminated with Cd; and strongly contaminated with Hg. Heavy metal content in the sediments were found to be significantly influenced by different physico-chemical parameters. The effect of these physico-chemical parameters canbe arranged in the following order: clay fraction > organicmatter fractions > carbonate fraction > silt fraction. As sequential extraction procedure shows that the total concentration of the heavy metals are largely bound to the residual phase (retained 79.5% of Pb, 38% of Cd, 54.4% of Zn and 51.6% of Fe in Jordan River Sediments; and 88.6% of Pb, 48.2% of Cd, 37.6% of Zn and 59.5% of Fe in the YarmoukRiver sediments). The following sequence of mobility are suggested: Fe > Cd > Zn > Pb in Jordan River sediments, and Fe > Zn > Cd > Pb. in Yarmouk River sediments.     

Concentrations and forms of heavy metals in Slovak soils

The risk assessment of heavy‐metal contamination in soils requires knowledge of the controls of metal concentrations and speciation. We tested the relationship between soil properties (pH, CEC, C_org, oxide concentrations, texture) and land use (forest, grassland, arable) and the partitioning of Al, Cd, Cr, Cu, Fe, Mn, Ni, Pb, and Zn among the seven fractions of a sequential extraction procedure in 146 A horizons from Slovakia. Using a cluster analysis, we identified 92 soils as representing background metal concentrations while the remaining 54 soils showed anthropogenic contamination. Among the background soils, forest soils had the lowest heavy‐metal concentrations except for Pb (highest), because of the shielding effect of the organic layer. Arable soils had the highest Cr, Cu, and Ni concentrations suggesting metal input with agrochemicals. Grassland soils had the highest Cd and Zn concentrations probably for geogenic reasons. Besides the parent material (highest metal concentrations in soils from carbonatic rock, lowest in quartz‐rich soils with sandy texture), pedogenic eluviation processes controlled metal concentrations with podzols showing depletion of most metals in E horizons. Partitioning among the seven fractions of the sequential extraction procedure was element‐specific. The pH was the overwhelming control of the contributions of the bioavailable fractions (fractions 1–4) of all metals and even influenced the contributions of Fe oxide‐associated metals (fractions 5 and 6) to total metal concentrations. For fractions 5 and 6, Fe concentrations in oxides were the most important control of contributions to total metal concentrations. After statistically separating the pH from land use, we found that the contributions of Cu in fractions 1–4 and of NH₄NO₃‐extractable Al, Cd, Pb, and Zn to total metal concentrations were significantly higher under forest than under grassland and in some cases arable use. Our results confirm that metal speciation in soils is mainly controlled by the pH. Furthermore, land use has a significant effect.     

杭州市城市土壤中重金属、磷和其它元素的特征

Health implications of inhaling and/or ingesting dust particles with high concentrations of heavy metals from urban soils are a subject of intense concern. Understanding the geochemistry of these metals is key to their effective management. Total concentrations of heavy metals, phosphorus (P) and 8 other elements from topsoil samples collected at 82 locations in Hangzhou City were measured to: a) assess their distribution in urban environments; and b) understand their differentiation as related to land use. Metal mobility was also studied using a three-step sequential chemical fractionation procedure. About 8.5%, 1.2%, 3.6%, 11.0% and 30.3% of the soil samples had Cd, Cr, Cu, Pb, and Zn concentrations, respectively, above their allowable limits for public and private green areas and residential use. However, in commercial and industrial areas, most samples had metal concentrations below their allowable limits. Statistical analyses revealed that the 16 measured elements in urban soils could be divided into four groups based on natural or anthropic sources using a hierarchical cluster analysis. Additionally, Cu, Pb, and P showed similar spatial distributions with significant pollution in commercial zones, suggesting vehicle traffic or commercial activities as dominant pollutant sources. Also, Cd, Co, Cr, Ni, Zn, Mn and Fe had the highest concentrations in industrial locations, signifying that industrial activities were the main sources of these seven metals. Moreover, the data highlighted land-use as a major influence on heavy metal concentrations and forms found in topsoils with large proportions of soil Cd, Co, Cr, and Ni found in residual fractions and soil Cu, Pb and Zn mainly as extractable fractions.     

The identification of point sources of heavy metals in an industrially impacted waterway by periphyton and surface sediment monitoring

Periphyton and sediment samples were collected from 12 stations along Bayou d'Inde, a very polluted waterway, in Southwestern Louisiana. The samples were analyzed for Zn, Cu, Pb, Ni, Fe, Cr, Al, Cd, and Ag. When metal concentrations in periphyton or sediment are plotted vs sampling station, the metal distributions clearly indicate a major point source of metals at one station which is located at the mouth of an industrial ditch. Metal levels in periphyton generally parallel those found in surface sediments at the same location, but metal levels in periphyton are generally higher than in sediment from the same location, indicating an enrichment over sediment values. For sediments two types of extraction were investigated using leaching with concentrated HNO₃ in a high-pressure decomposition vessel and shaking with 1 N HCl for 2 hr. Both methods correlate well for all metals except Ni, but HNO₃ extracted more total metal. Correlations between periphyton and sediment were best for Pb, Fe, and Ag. Poorest correlations were seen for Mn, Ni, and Cd. When periphyton and sediment metal concentrations were normalized to Fe, Mn, and Al, correlation factors for some metals improved while others deteriorated.     

Fractionation and Distribution of Metals in Guadiamar River Sediments (SW Spain)

Traditionally, the Guadiamar River (Seville, Southwest Spain) has received pollution from two different sources, in its upper section, from a pyrite exploitation (Los Frailes mine) and, in its lower section, from untreated urban and industrial wastes and from intensive agricultural activities. In 1998, the accidental spillage of about 6 million m³ of acid water and sludge from mine tailings to Guadiamar River worsened the pollution of an already contaminated area. The main polluting agents of the spillage were heavy metals. The total concentration of a metal provides scarce information about the effects on environmental processes or about the toxicity of the sediment samples. A more sophisticated fractionation of the sediment samples based on a species distribution can help to understand the behaviour and fate of the metals. This article describes a distribution study of the metals Al, Cd, Cu, Fe, Mn, Pb and Zn by fractionation analysis of sediments from eleven sample sites alongside the Guadiamar Riverbed. The samples were collected in summer 2002, four years after the spillage and after the area had been cleaned. Sequential extraction analysis resulted in the definition of four fraction categories: exchangeable metal (the most available fraction), reducible metal (bound to hydrous oxides of Fe and Mn), oxidizable metal (bound to organic matter and sulphides) and a residual fraction (bound to minerals). Significant increases in the available fraction of several potentially toxic metal ions like Cd, Mn and Zn were found. The distribution pattern was variable along the River. At the site closest to the mineworks, the soluble forms of Cd, Mn and Zn were significantly more abundant that those downstream. Cu and Pb were present in the reducible fraction while Fe was present associated in the residual fraction.     

Changes of Al and Heavy Metal Concentrations in Slovak Soils During the Last 25 Years

The objective of this study was to investigate changes of total concentrations and various extract-defined Al and heavy metal fractions in Slovak agricultural soils during the last 25 years. We compared 7 stored soil samples collected between 1966 and 1970 with samples collected in 1994 at the same sites. Seven fractions of Al, Cd, Cr, Cu, Fe, Mn, Ni, Pb, and Zn were determined with a sequential extraction procedure in all samples. Total concentrations of Cd, Zn, Mn, Ni, and Cu were lower in the 1994 samples; those of Al, Fe, Pb, and Cr were higher. Based on the initial concentrations, the average total concentration changes were: Cd(-10,3%)<Zn(-7,2%)<Mn(-4,8%)<Ni(-2,3%)<Cu(-1,4%)<Al(+2,1%)<Fe(+2,9%)<Cr(+7,4%)<Pb(+8,3%). This row is consistent with the decrease in metal mobility. The differences in salt-extractable metals showed the same pattern; however, changes were more pronounced than for total concentrations. The results suggest that decreases during the last 25 years are caused by higher leaching than deposition rates and increases vice versa. The highest increase in Cr and Pb concentrations is observed in the EDTA-extractable fraction, which mainly characterizes organically bound metals.     

Variations of trace element concentrations in red spruce tree rings

The potential of coniferous trees as biological indicators of heavy metal atmospheric pollution was investigated. In 31 municipalities of an industrialized region, samples of wood from the trunks of red spruce (Picea rubens) were taken to determine the spatial distribution of accumulated metals. Using the annual rings, these core samples were divided into 5-yr sections to determine temporal variations. The concentrations of Mg, Al, Ca, Mn, Fe, Cu, and Zn were measured by neutron activation analysis. All metals showed the highest concentrations in the most recent wood and the bark. For the wood older than 5 yr, Mn and Zn are stable with time, Mg and Ca decrease, while Al, Fe, and Cu appear to increase. A statistical analysis showed the municipalities with the highest variations in metal concentrations; it also revealed correlations in the fluctuations of several of the metals. As expected, trees in towns near metal refineries contain higher amounts of Mn, Fe, and Al. Large variations in metal concentrations, due to factors not totally understood, were observed. Thus, red spruce is not a sensitive bio-indicator of atmospheric metal pollution.     

The Influence of Sediment Sources and Hydrologic Events on the Nutrient and Metal Content of Fine-Grained Sediments (Attert River Basin, Luxembourg)

Nutrient (C, N and P) and metal (Cr, Cu, Ni, Pb and Zn) content and dynamics of suspended and channel bed sediments were analysed within the rural Attert River basin (Luxembourg). This basin is representative of the main physiographic characteristics of the country, where there is currently little information available on the composition and dynamics of fluvial sediment. Stream bed fine-grained sediment samples (n?=?139) collected during low flow conditions and time-integrated suspended sediment samples (n?=?183) collected during storm runoff events (October 2005 to April 2008) in seven nested basins ranging from 0.45 to 247?km² were analysed. Nutrient and metal spatial patterns, temporal trends and the relationship between their content and storm runoff characteristics (e.g. maximum discharge and sediment concentration) were assessed. Results showed a high spatial and temporal variability, mainly associated with basin characteristics and local inputs. Higher values of total C were measured in the highly forested basins located in the northern part of the Attert River basin, whereas the highest values of total P were mainly associated with material coming from grassland and with the inflow of wastewater treatment plants (i.e. higher values of total P were measured in the southern part of the basin). The abundance of metals, not only in suspended but also in channel bed sediments, was generally as follows: Zn > Cr > Ni > Pb > Cu. Both nutrient and metal concentrations were at a maximum at the beginning of the wet season, after having been accumulated during the summer. These values tended to decrease during autumn and winter due to sediment mobilisation, and a higher flow capacity to transport coarser particle fractions from the sources. In general, concentrations of nutrients and metals on suspended sediment were negatively correlated with antecedent precipitation, total precipitation, total specific discharge and maximum discharge, which has been previously associated to a ??dilution?? effect during storm runoff events. Results show that both sediment sources and hydrologic events play an important role on the spatial and temporal variability of sediment-associated nutrient and metal contents.     

Assessment of Heavy Metal Pollution in the Sediments of the River Pra and Its Tributaries

An investigative study was conducted to determine the heavy metal pollution in the sediment in the Pra Basin of Ghana from 27 sampling points during the dry and wet seasons using the geo-accumulation index (Igeo), enrichment factor (EF), and pollution load index (PLI). Sediments were acid digested and analyzed for the following selected metals: arsenic (As), lead (Pb), cadmium (Cd), zinc (Zn), manganese (Mn), total chromium (Cr), nickel (Ni), and iron (Fe) using the dual atomizer and hydride generator atomic absorption spectrophotometer (model ASC-7000 No A309654, Shimadzu, Japan). The metal concentrations (mg kg^?1) in the sediments were as follows: As (0.175)?<?Cd (3.206)?<?Ni (79.927)?<?Zn (118.323)?<?Cr (216.708)?<?Mn (234.742)?<?Pb (335.381)?<?Fe (1354.513) in the dry season and As (0.002)?<?Cd (7.279)?<?Ni (72.663)?<?Zn (35.622)?<?Pb (135.863)?<?Cr (167.604)?<?Mn (183.904)?<?Fe (1138.551) for the wet season. The EF which is an indication of whether metal concentrations are due to anthropogenic activities shows enrichment at all site for the metals Cr, Pb, and Cd in the wet seasons. However, only 4 out of the 27 sites showed Ni enrichment in the wet season. Contrary to the wet season, only Pb and Cr recorded enrichment at all sites during the dry season. Fifteen out of the 27 sites recorded Cd enrichment and 24 out of the 27 sites recorded Ni enriched during the dry season. None of the sites were enriched with Fe, As, Zn, and Mn in either the dry or wet seasons. For both dry and wet seasons, the pollution load index for all the sites except one was at the background levels which is a sign of non-deterioration of the sites studied. In the wet season, the calculated Igeo reveals that the study area is not contaminated with respect to As, Zn, Fe, and Mn; uncontaminated to moderately contaminated with Cd; moderately contaminated with Cr; uncontaminated to moderately to heavily contaminated with Ni; and moderately to heavily contaminated with Pb. The dry season Igeo results reveal non-contamination of the study area with respect to As, Fe, and Mn; uncontaminated to moderately contaminated with Zn; moderately contaminated with Cr; uncontaminated to heavily contaminated with Cd; uncontaminated to extremely contaminated with Ni; and moderately to extremely contaminated with Pb. The high levels of Cd, Pb, and Cr in all the sites are due to unregulated illegal mining activities occurring in and around the study area. It is hoped that this study will prompt the basin management board to improve their management strategies in controlling unregulated illegal mining in the basin sediments.     

Predicting sediment metal concentrations in lakes without point sources 1

Surficial sediments (0 to 2 cm) from 189 sites in 52 Quebec and Ontario lakes were analyzed for Al, Co, Cr, Cu, Fe, Mn, Ni, Pb, and Zn by atomic adsorption spectrometry after extraction in dilute aqua regia. Empirical models using sediment texture (water content), site morphometry (depth) and geology (categorical variables) as predictors explain 82 to 87% of the between-site and between lake variation in sediment concentrations of Cu, Cr, Ni, Pb, and Zn, and 52 to 68% of the variation of Al, Co, Fe, and Mn. Over a broad geologic range, geologic variables are only significant in models predicting Co, Cr, and Ni. These three elements are low in concentration in lakes with catchments on the Grenville shield, while Cr and Ni are enriched in catchments containing ophiolite geology. These models explain both between-site and between-lake variation in sediment metal concentrations, and due to the lack of geologic influence on most metals, may be valid for other regions. The models appear promising as a means to identify point source contamination without assumptions about the relevant sediment fractions or inter-element relationships.     

三峡库区重金属含量空间分布及污染状况

[目的]对三峡库区坡面土壤与消落带沉积泥沙中重金属含量特征开展研究,为该区重金属污染评价提供理论与数据支持。[方法]在三峡库区选取53个采样点,分析区域内坡面土壤与消落带沉积泥沙中Cr, Cu, Pb, Zn, Mn 5种重金属元素的含量,利用单因子污染指数法、内梅罗综合指数法、地累积指数法和潜在生态风险指数法开展污染状况评价。[结果]研究区域内重金属含量平均值大小依次为:Mn>Zn>Cr>Cu>Pb,仅Cu, Zn和Mn存在污染。Zn和Mn在消落带沉积泥沙与坡面土壤中皆富集,而Cu仅在坡面土壤中富集。研究区域内重金属在空间分布上呈上、下游高,中游低分布。单因子污染指数法表明,研究区内仅存在Zn(P_ia=1.07)的轻度污染与Mn(P_ia=2.65)的中度污染。研究区域内梅罗综合指数为2.93,为中度污染。根据地累积指数法,研究区域内仅存在Mn轻度污染,其余重金属皆为无污染。Cr, Cu, Pb, Zn, Mn的潜在生态危害皆为轻微生态危害;研究区域的综合生态危害指数为14.09,为轻微生态危害。[结论]研究区域内Cr...     

Assessment of heavy metal pollution in surface sediments of the Montenegrin coast: a 10-year review

Purpose

Heavy metals are among the most common environmental pollutants, which can be introduced into coastal areas from natural and anthropogenic sources, and thereby possibly impact marine organisms and human population. Therefore, the aim of this study was to evaluate the pollution level of Montenegrin coastal sediments by determining the concentrations of 10 metals and metalloids (Fe, Mn, Zn, Cu, Ni, Pb, Cr, Cd, As, and Hg) during one whole decade.

Materials and methods

Sediment samples were collected from 11 sites along the Montenegrin coast during the 2005–2016 exposure to different levels and sources of anthropogenic impact. The extent of pollution was estimated by determining total element concentrations in the sediment. Mineralized samples were analyzed for Cu, Ni, Fe, Mn, Cr, As, Pb, Zn, Cd, and Hg. Pollution status was evaluated using the contamination factor, pollution load index, and geo-accumulation index, as well as statistical methods, such as Pearson correlation coefficient (r) and cluster analysis (CA).

Results and discussion

This study showed that concentrations of individual metals at some locations were extremely high. The metal concentrations (in mg kg^?1) ranged as follows: Fe 1995–45,498; Mn 135–1139; Zn 10–1596; Cu 3.8–2719; Ni 2.94–267; Pb 0.1–755; Cr 2.5–369; Cd 0.1–5.4; As 0.1–39.1; and Hg 0.01–14.2. The calculated concentration factor and pollution load index indicates enrichment by either natural processes or anthropogenic influences. The geo-accumulation index value (Igeo) showed that one location was strongly or extremely polluted (3.78?<?Igeo ≤?6.15) with Hg in all investigated years, while extreme Igeo values for four bioactive elements, Pb, Cd, Cu, and Zn, were found in only a few single samples.

Conclusions

On the basis of the obtained values, it can be concluded that generally higher metal contents were distributed in Boka Kotorska Bay sites, although some extreme values were also recorded at the locations outside of the Bay. Geo-accumulation index and pollution load index showed that the metal levels were high enough to pose risk to the ecosystem.

     

Assessing the Removal Efficiency of Zn, Cu, Fe and Pb in A Treatment Wetland Using Selective Sequential Extraction: A Case Study

The accumulation and speciation of Zn, Cu, Fe and Pb in the sediments of an artificial surface-flow wetland used to treat domestic wastewater near Christchurch, New Zealand, were examined. Water metal concentrations and total suspended solid (TSS) content were determined at the inflow and outflow both in winter and summer, and metal concentrations were analysed in shoots and roots of selected plants. Water and sediment data suggest that the wetland is acting as a sink for Zn, Cu and Pb, while Fe uptake is minimal and the wetland appears to be releasing Fe in the winter. Metal concentrations in the most mobile fractions (exchangeable and bound to carbonates) are negligible. Cu is mostly associated with the organic/sulphide phase, whereas Zn and Pb show a strong affinity for hydroxides and organics/sulphides. A large fraction of all metals is also present in the residual phase, and is therefore unlikely to be released into the overlying water. Metal concentrations are below the low trigger values of the ANZECC sediment quality guidelines, except for Pb near the inflow. However, results of sequential extraction suggest that a significant proportion of Pb occurs in the detrital phase and is therefore not bio-available. Metal concentrations were higher in the roots than in the shoots of both Juncus sp. and Lythrum hyssopifolia. This study shows that, although metal concentrations are low, TSS and metals, except Fe, are effectively removed by the wetland system. The low removal rate of Fe is possibly due to the young age of the wetland and low loading rates.