Carcinogenic risk evaluation for human health risk assessment from soils contaminated with heavy metals

Human activities have progressively increased in recent years. Consequently, significant environment deterioration resulted. Soils have a particularly varied vulnerability to heavy metal pollution, especially in the vicinity of industrial areas. Heavy metal contamination of soil may induce risks and hazards to humans and the ecosystem, while toxic metals in soil can severely inhibit the biodegradation of organic contaminants. This paper is focused on human health risk assessment from extremely contaminated soil with heavy metals, mainly with carcinogenic elements. The study refers to an agricultural area in the vicinity of an old metallurgical processing industrial facility. The contaminants evaluated in the present paper are beryllium (Be), cadmium (Cd), chromium (Cr), nickel (Ni) and lead (Pb). Contamination level is pointed out through laboratory analysis results of soil samples taken from 0–0.2 m, 0.2–0.4 m soil layers and up to 2.1 m soil depth. Some heavy metal concentrations (Cd, Cr and Pb) exceed the intervention thresholds for sensitive areas, as they are stipulated in the national regulation in Romania. The identified average concentration levels of Cd, Cr^VI and Pb in the first layer of the investigated land are 23.83, 7.71 and 704.22 mg/kg_d.w, respectively. The results show that the potential risk of human health is relevant (higher than the acceptable one after World Health Organization) and a possible solution for the remediation should become a major concern for the investigated area.     

Dissolved sulfides in the oxic water column of San Francisco Bay,California

Trace contaminants enter major estuaries such as San Francisco Bay from a variety of point and nonpoint sources and may then be repartitioned between solid and aqueous phases or altered in chemical speciation. Chemical speciation affects the bioavailability of metals as well as organic ligands to planktonic and benthic organisms, and the partitioning of these solutes between phases. Our previous, work in south San Francisco Bay indicated that sulfide complexation with metals may be of particular importance because of the thermodynamic stability of these complexes. Although the water column of the bay is consistently well-oxygenated and typically unstratified with respect to dissolved oxygen, the kinetics of sulfide oxidation could exert at least transient controls on metal speciation. Our initial data on dissolved sulfides in the main channel of both the northern and southern components of the bay consistently indicate submicromolar concenrations (from <1 nM to 162 nM), as one would expect in an oxidizing environment. However, chemical speciation calculations over the range of observed sulfide concentrations indicate that these trace concentrations in the bay water column can markedly affect chemical speciation of ecologically significant trace metals such as cadmium, copper, and zinc.     

氨基泡塑的合成及其应用于富集地质样品中的痕量金

采用泡塑(PUF)富集,AAS或ICP-OES测定地质样品中痕量金是常用的分析方法。与活性炭相比,PUF的选择性好,但吸附容量偏低,可将泡塑负载不同的萃取剂或修饰不同的官能团提高吸附容量。本文将聚醚型泡塑经盐酸水解制备成氨基泡塑(PUF-NH_2)。红外光谱和扫描电镜表征显示,PUF-NH_2峰形发生了明显红移(3376.5 cm-1),其中的氨基数量显著增加,另外PUF-NH_2的高分子出现明显断裂,发生水解后裸露出的氨基具有还原性,在吸附金的过程中易与金离子在PUF-NH_2表面发生氧化还原反应,形成金纳米颗粒。改性后的PUF-NH_2吸附容量达到96 mg/g,与PUF相比提高了8倍。将PUF-NH_2应用于富集地质样品中的金,经炭化灼烧、50%王水提取后用ICP-OES测定,金的加标回收率在95.0%~105.0%之间,检出限为0.15μg/g。实验证明用PUF-NH_2处理样品提高了富集倍数和分析灵敏度,有利于低品位矿石的分析。     

Biosorption of heavy metals by organic carbon from spent mushroom substrates and their raw materials

The use of agricultural wastes as biosorbents is gaining importance in bioremediation of heavy metal-polluted water and soils, due to their effectiveness and low cost. This work assesses the Cd, Pb and Cu adsorption capacity of the raw materials used in the production of substrates for mushroom production (Agaricus bisporus and Pleurotus ostreatus) and the spent mushroom composted (SMC), based on the functional groups of their organic carbon. The raw materials studied included agricultural wastes (wheat straw, wheat and rice poultry litter, grape pomace) and inorganic substances (gypsum and calcareous sand). Organic carbon from wastes and their composting products were characterized by CP-MAS ¹³C NMR. Langmuir adsorption isotherms of metals were plotted for each raw material, composting step, spent A. bisporus and P. ostreatus substrates and the final SMC. The maximum adsorption capacities of SMC were 40.43, 15.16 and 36.2 mg g^?1 for Cd, Pb and Cu, respectively. The composting process modified the adsorption properties of raw materials because of the enhanced adsorption of Cd and Cu and decreased adsorption capacity of Pb. CP-MAS ¹³C NMR and potentiometric titration were used to identify the functional groups of the organic carbon responsible for the metal adsorption. The content of cellulose was correlated with Pb adsorption (p < 0.001), alkyl and carboxyl carbon with Cd adsorption (p < 0.001), and N-alkyl (p < 0.001) and carboxyl (p < 0.010) groups with Cu adsorption. These results are valuable to develop new biosorbents based on agricultural wastes and demonstrate the high potential of SMC to adsorb heavy metals from polluted environments.     

Comprehensive analysis of heavy metals in soils from Baoshan District, Shanghai: a heavily industrialized area in China

The potential for soil heavy metal contamination in high risk areas is a crucial issue that will impact the environment. Soil samples were collected in 2003 and 2007 to investigate heavy metal contamination characteristics and pollution changes in the industrialized district of Baoshan (Shanghai, China). Both multi-statistic and geostatistic approaches were used and proved to be useful in the interpretation of the analytical results. The potential for soil contamination in the high risk areas presents a crucial issue that will impact the environment. The results indicate that soil in the Baoshan District is alkaline. Additionally, the accumulation of heavy metals in the soil increased between 2003 and 2007. The study results indicated that the concentration of the metals lead (Pb), chromium (Cr), cadmium(Cd), mercury (Hg), arsenic (As), zinc (Zn) and copper (Cu) in the soil has great discrepancy, especially of Pb and Cr. The concentrations of Pb and Cr in the soil show significant difference between two observed years (p?<?0.05). The concentration of most of these metals was higher in 2007 than 2003. Only the concentrations of Cd and As were not higher in 2007. Traffic and industrial contaminants were the likely source of Pb and As; Hg largely came from agricultural contamination, household garbage and industrial contamination; Cd, Cr, Zn and Cu mainly originated from industrial activities. Multivariate statistical analyses showed that human activities mainly contributed to heavy metal contamination. Spatial distribution confirmed this by showing that areas with the highest metal concentrations occurred where there were high levels of industrial activity and traffic. Potential ecological risk assessment results showed that high risk zones were highly correlated with spatial analysis. The study estimated that in 2007, 85.2?% of the district could be categorized as high risk, which is 77.4 times more than that in 2003.     

pH influence on sorption characteristics of heavy metal in the vadose zone

Sorption is an important process in the modelling and prediction of the movement of heavy metals in unsaturated clay barriers. This experimental study investigates the effect of pH changes in the acidic range on the sorption characteristics of heavy metals such as: lead, copper and zinc in an unsaturated soil. A series of one-dimensional coupled solute and moisture leaching column tests, using different heavy metal solutions, were conducted on an unsaturated illitic soil at varying pH values. Variations of volumetric water content (VWC) with distance were measured for different time durations, and concentrations of heavy metals in the liquid and solid phases were analysed. Partitioning coefficient profiles of contaminants along the soil column were determined for each individual layer in the soil.

Results from column leaching tests showed that the sorption characteristics of heavy metals are controlled by many factors which should be taken into consideration, i.e. the VWC, time of wetting, soil pH, and the influent heavy metal concentrations. Simplification of K_d as a constant and of the VWC as a linear function cannot be considered a good assumption and may lead to an improper evaluation of the sorption phenomena and also to serious errors in predicting contaminant transport through unsaturated soils.     

广西岩溶区土壤铁锰结核重金属富集的地质特征

广西岩溶区农田土壤重金属污染形势严峻。该地区土壤含有大量铁锰结核,其主要成分为铁和锰的氧化物,对重金属有着较强的富集作用。铁锰结核伴随着土壤形成过程而产生,也是反映土壤形成过程及成土环境变化的良好载体。研究铁锰结核中重金属的富集特征有助于了解广西岩溶区土壤中重金属元素的富集过程和富集特征。文章对广西柳江和桂平的土壤与其中的铁锰结核进行了成分分析,通过微量元素分析得到铁锰结核对Ni、Cu、Cd、Zn、Pb、Co、Ba、As、Cr等重金属元素的富集特征,通过Ti/Al2O3的比值关系推断了铁锰结核与土壤的物质来源。此外,还对铁锰结核进行了激光共聚焦显微拉曼光谱仪（Laser Microscopic Confocal Raman Spectrometer）、扫描电镜和能谱仪（SEM-EDS）分析。通过铁锰结核内部同心环带状圈层结构及其内部的元素分布周期性变化的特征,推测结核形成机制。铁锰结核的形成固定了大量重金属元素,减轻了土壤重金属污染负担;但如果铁锰结核发生了溶解则会导致Mn及受其控制的部分重金属（Co、Cu、Ni、Ba）重新释放回到土壤,加重重金属污染。     

Adsorption characteristics of heavy metals in soil zones developed on spilite

Various soil zones such as Bw, C1, and C3 are developed on spilite. Montmorillonite, vermiculite and chlorite is moderately occurred in the C1 and C3 soil zones, in contrast montmorillonite and vermiculite are absent in Bw soils whereas illite and sesquioxide are relatively increased. The high cation exchange capacity (CEC) of montmorillonite and vermiculte and moderate CEC of chlorite and illite resulted in the high adsorption of heavy metals. The adsorption of the heavy metals on spilite soil zones was studied at different concentrations and pH levels. Heavy metals like lead, cadmium, and copper were selected for adsorption studies considering their contribution as toxic metals in the environment. The initial solute concentrations ranged from 7.0 × 10⁻³ to 1.0 × 10² mg/L. The sorption behavior of Cd²⁺, Pb²⁺, and Cu²⁺ on soil zones of spilite was investigated using the batch equilibrium technique at 25°C. The characteristics of the adsorption process were investigated using Scatchard plot analysis (q/C vs. q) by the batch equilibrium technique at 25°C. In the adsorption of heavy metals, deviation from linearity in the plot of q/C versus q was observed, indicating the presence of multi-model interaction and non-Langmuirean behavior. When the Scatchard plot showed a deviation from linearity, greater emphasis was placed on the analysis of the adsorption data in terms of the Freundlich model, in order to construct the adsorption isotherms of the metal(s) at particular concentration(s) in solutions. The adsorption behavior of these metal ions on spilite soil zones is expressed by the Freundlich isotherms. Adsorption constants and correlation coefficients for the Cd, Pb, and Cu on spilite soil zones were calculated from Freundlich plots.     

Assessment of heavy metal pollution in soils around a paper mill using metal fractionation and multivariate analysis

Effects of paper mill wastes on the status of soil copper (Cu), manganese (Mn) and zinc (Zn) in and around 16 sites near a paper mill in Assam, North East India (26°07.485′ to 26°07.915′ N latitude and 92°12.706′ to 92°15.065′ E longitude), have been investigated in the present study. The six-step sequential extraction techniques revealed that the water-soluble fraction had the least contribution (below detectable limit to 3.24 mg kg^?1 of Cu, 13.87 mg kg^?1 of Mn and 1.25 mg kg^?1 of Zn) towards soil contamination, irrespective of the metals evaluated. Chemical fractionation of Cu, Mn and Zn in majority of the sampling locations showed non-homogenous orders of contamination. Comparison of the magnitude of local and individual heavy metal contamination factors against global values showed that the places near the paper mill waste disposal site displayed higher potential risk from metal contamination. Furthermore, the mobility factor related to ecotoxicity of soil environment was found to be metal specific and depended not only on total metal concentration but also on the nature of metal in the order Mn > Cu > Zn.     

Spatio-temporal dynamics of heavy metals in sediments of the river estuarine system: Mahanadi basin (India)

Dynamics of heavy metals in the surface sediments of Mahanadi river estuarine system were studied for three different seasons. This study demonstrates that the relative abundance of these metals follows in the order of Fe > Mn > Zn > Pb > Cr > Ni ≥ Co > Cu > Cd. The spatial pattern of heavy metals supported by enrichment ratio data, suggests their anthropogenic sources possibly from various industrial wastes and municipal wastes as well as agricultural runoff. The metal concentrations in estuarine sediments are relatively higher than in the river due to adsorption/accumulation of metals on sediments during saline mixing, while there is a decreasing trend of heavy metal concentrations towards the marine side. The temporal variations for metals, such as Fe, Mn, Zn, Ni and Pb exhibit higher values during monsoon season, which are related to agricultural runoff. Higher elemental concentrations are observed during pre-monsoon season for these above metals (except Ni) at the polluted stations and for metals, such as Cr, Co and Cd at all sites, which demonstrate the intensity of anthropogenic contribution. R-mode factor analysis reveals that “Fe–Mn oxy hydroxide”, “organic matter”, “CaCO₃”, and “textural variables” factors are the major controlling geochemical factors for the enrichment of heavy metals in river estuarine sediment and their seasonal variations, though their intensities were different for different seasons. The relationships among the stations are highlighted by cluster analysis, represented in dendrograms to categorize different contributing sites for the enrichment of heavy metals in the river estuarine system.     

Heavy metal assessment and water quality values in urban stream and rain water

Water quality monitoring in developing countries is inadequate, especially in stream water affected by urban effluents and runoff. The purpose of this study was to investigate heavy metal contaminants in the Nakivubo Stream water in Kampala, Uganda. Water samples Nakivubo Channelized Stream, tributaries and industrial effluents that drain into the stream were collected and analysed for the total elemental concentration using flame atomic absorption spectrophotometer. The results showed that: 1) the wastewater was highly enriched with lead and manganese above the maximum permissible limit; 2) the levels of dissolved oxygen were below the maximum permissible limit, while the biological oxygen demand was above the maximum permissible limit. All industrial effluents/wastewater were classified as strong (> 220 mg/L). Factor analysis results reveal two sources of pollutants; 1) mixed origin or chemical phenomena of industrial and vehicular emissions and 2) multiple origin of lead (vehicular, commercial establishment and industrial). In conclusion, Nakivubo Channelized Stream water is not enriched with heavy metals. These heavy metals (lead, cadmium and zinc) were rapidly removed by co-precipitation with manganese and iron hydroxides and total dissolved solids into stream sediments. This phenomena is controlled by pH in water.     

Competitive adsorption of Cd,Cu, Pb and Zn by different soils of Eastern China

Simultaneous competitive adsorption behavior of Cd, Cu, Pb and Zn onto nine soils with a wide physical–chemical characteristics from Eastern China was measured in batch experiments to assess the mobility and retention of these metals in soils. In the competitive adsorption system, adsorption isotherms for these metals on the soils exhibited significant differences in shape and in the amount adsorbed. As the applied concentration increased, Cu and Pb adsorption increased, while Cd and Zn adsorption decreased. Competition among heavy metals is very strong in acid soils with lower capacity to adsorb metal cations. Distribution coefficients (K _dmedium) for each metal and soil were calculated. The highest K _dmedium value was found for Pb and followed by Cu. However, low K _dmedium values were shown for Zn and Cd. On the basis of the K _dmedium values, the selectivity sequence of the metal adsorption is Pb > Cu > Zn > Cd and Pb > Cu > Cd > Zn. The adsorption sequence of nine soils was deduced from the joint distribution coefficients (K _dΣmedium). This indicated that acid soils with low pH value had lower adsorption capacity for heavy metals, resulting in much higher risk of heavy metal pollution. The sum of adsorbed heavy metals on the soils could well described using the Langmuir equation. The maximum adsorption capacity (Q _m) of soils ranged from 32.57 to 90.09 mmol kg⁻¹. Highly significant positive correlations were found between the K _dΣmedium and Q _m of the metals and pH value and cation exchange capacity (CEC) of soil, suggesting that soil pH and CEC were key factors controlling the solubility and mobility of the metals in soils.     

The application of diffusion–reaction mixed model to assess the best experimental conditions for bark chemical activation to improve copper(II) ions adsorption

Natural sorbents have been thoroughly assessed to determine their adsorption capabilities to remove pollutants from industrial wastewaters. Among them, pine bark has demonstrated potential for carrying out the removal of contaminants, particularly heavy metals, at the level of traces present in dissolved state. Nevertheless, to move towards the wastewater treatment implementation at large scale, the handling and processing requirements of pine bark to optimise the adsorption of heavy metals must be fully assessed. This research study presents a new mathematical model to evaluate the impact of acid pre-treatment of pine bark on heavy metals adsorption at different pine bark-aqueous solution pulp densities. A diffusion–reaction mixed model was developed and applied to the case study of copper(II) adsorption onto pine bark. The low binding energy inferred from analysing the adsorption isotherms suggested that a diffusive mechanism is governing the whole process. The mixed diffusion–reaction kinetic model indicated that the activation increases the rate at which metal ions are adsorbed, but it reduces the maximum achievable adsorption which in turn restricts its usefulness to relatively high pulp densities (above 10 g/L). The latter constitutes the first step towards optimising the use of bark pine for treating wastewater polluted with heavy metals and for establishing rules for scaling-up the process.     

The impacts of common ions on the adsorption of heavy metal

Researches on the impact of common ions onto sediments are of great importance for the study of the heavy metal adsorption mechanisms. Considering the surface sediments from the relatively clean reach in the Baotou section of the Yellow River as the adsorbent, this work presents the impacts of common ions (Na⁺, Mg²⁺, K⁺, Ca²⁺, Cl⁻, SO₄ ²⁻, and NH₄ ⁺) on heavy metals (Cu²⁺, Zn²⁺, Cd²⁺, and Pb²⁺) adsorption. The experimental results reveal that the adsorptive capacities of the heavy metals are controlled by different adsorption mechanisms in different ion concentration ranges. With the increase of the ionic strength, the adsorption of the heavy metals increases for the compression of the electric double layer, whereas decreases for the decreasing of the ionic activities of the heavy metals. The competitive adsorption and complexations between the heavy metals and common ions are also important factors controlling the heavy metal adsorption. According to the experimental results and the real concentration of common ions in the Baotou section of the Yellow River, the increase of the concentrations of Na⁺, Mg²⁺, K⁺, and Ca²⁺ would cause the increase of Zn²⁺ adsorption and reduce the Zn pollution. The NH₄ ⁺ from the industrial discharge of the tributaries has a strong impact on the heavy metal adsorption.     

Investigation of elemental enrichment and ecological risk assessment of surface soils in two industrial port cities,southwest Iran

In recent years, there has been a rapid growth in the two industrial port cities of Iran, the port of Mahshahr and the port of Imam Khomeini. In spite of their importance for the economy, the two cities require monitoring and assessment from an environmental and human health perspective. In this study, environmental quality and heavy metals pollution of soils influenced by human activities were investigated. A total of 30 soil samples were collected and subjected to detail physicochemical characterization. The results showed high levels of heavy metals in the urban soils of port of Mahshahr (POM) and elevated respective levels in surface soils of the port of Imam Khomeini (PIK) with Ni being significantly higher than those in POM. The integrated pollution index (IPI) values of metals ranged from 1.22 to 1.87 in POM and 1.52 to 3.31in PIK, 50% of soil samples in PIK were classified as highly polluted, and all of the soil samples in PM were classified as moderately polluted. These results are in accordance with Enrichment Factor (EF) values, which showed the role of anthropogenic activities in the soil heavy metal enrichment. Moreover, the highest potential ecological risk index (RI) was found in the sites of petrochemical industries in PIK indicating serious metal contamination. Statistical analysis showed that heavy metals were mainly controlled by human activities. The results showed more dense industrial activity in PIK is responsible for higher pollution. This study establishes a benchmark against which future monitoring and remediation programs can be based on. Because of proximity to the Persian Gulf, continued the release of contaminants into the region, could have adverse biological health effects.     

A Review of Study on Fe-C Interaction and Their Adsorption Properties to Soil Heavy Metal

Nowadays, the Fe-C coprecipitate mechanism is recognized by more and more scholars and becomes the hot topic in the environmental science. On the basis of discussing the interaction between iron oxide and organic matter, and the adsorption research progress of Fe-C complexes on heavy metals, the immobilization potential of Fe-C complexes on heavy metals in polluted soil were illustrated. The surface properties and physical characterizations of iron oxide are changed regularly with the interaction of organic matter, which lead to the higher adsorption capacity of Fe-C complexes in contrast to single iron oxide. Besides, the influences of pH values, organic matter types and surface properties of iron oxides on the adsorption capacity of Fe-C complexes on heavy metals were discussed. The excellent adsorption performance of Fe-C complexes in certain conditions will provide important theoretical basis for contaminated soil remediation.     

Application of chemometric methods to analyze the distribution and chemical fraction patterns of metals in sediment from a metropolitan river

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.     

Testing the ability of bentonite-amended natural zeolite (clinoptinolite) to remove heavy metals from liquid waste

 The design of environmentally sound liquid waste containment structures has become a crucial task in engineering applications due to ever increasing groundwater contamination from such sites. Construction of such structures usually requires a bottom liner of low hydraulic conductivity as part of the design. In order to reduce the hazards associated with liquid wastes including landfill leachate, bentonite-amended natural zeolite is proposed as an alternative to conventional earthen liners. Among many contaminants associated with liquid wastes, heavy metals are the most dangerous ones. This paper deals with determining the ability of natural zeolite to remove heavy metals from aqueous waste. For this purpose, crushed natural zeolite (clinoptinolite) is amended with commercial powdered bentonite to yield a soil mixture low in permeability and high in ion-exchange capacity. Leachate from a conventional landfill is used as the percolation fluid. Concentrations of certain heavy metals in the effluent fluid percolated through the bentonite-zeolite mixture are compared with that of initial leachate. The conclusion is reached that certain metals are efficiently removed from the influent solution by the soil matrix whereas some ions do not show significant reduction in concentration. This is attributed to high hydraulic conductivity of the bentonite-zeolite mixture.     

Quantitative spatial characteristics and environmental risk of toxic heavy metals in urban dusts of Shanghai,China

Associated with the rapid urbanization and industrialization, most of the urban parks and recreational areas in Shanghai are built close to major roads or industrial areas, where they are subject to many potential pollution source, including automobile exhaust and factory emissions. Urban dusts, containing many toxic heavy metals such as Pb, Cr, Cd, Hg and As, are one of main contributors for environmental pollution. In this study, 261 dust samples were collected from two different localities (streets and parks) in the urban area of Shanghai, China. Pb and Cr concentrations of all samples were determined by atomic adsorption spectrophotometer analyzer, and Cd, As and Hg concentrations in 74 samples by atomic fluorescence spectroscopy. The mean concentrations of Pb, Cr, Cd, As and Hg are 287, 157, 1.24, 8.73 and 0.16 mg kg⁻¹, respectively. Each heavy metal shows a wide range of concentration values. In comparison with heavy metal background values of soil in Shanghai, urban dusts have elevated metal concentrations as a whole, except those of As. The concentrations of Pb, Cr, Cd, As and Hg are 11.3, 2.1, 10.3, 0.997, 1.7 times of the soil background values, respectively. Compared with the global mean concentrations, Cr concentration in urban dusts is slightly higher. Pb, Cr and Hg show normal distribution after logarithmic transformation. Pb, Cr, Cd, As and Hg have second-order variation trends of the spatial distribution. The spatial distribution features of five toxic heavy metals, in general, illustrate relatively high levels within the regions of the inner-city ring highway and southwestern Shanghai. Cr and Cd are higher in Baoshan industrial park and the shipbuilding industries regions. The order of environmental risk is Pb > Cd > Cr > Hg > As. Pb and Cd have the highest risk for environment pollution and human health among the five metals. The pollutant sources of toxic heavy metals in Shanghai urban dusts are preliminarily concluded as follows: As may have mainly a natural source. Burning of coal has become the main source of Hg pollution. Pb, Cr and Cd have three sources, traffic, building construction, and weathering corrosion of building materials.     

武水河上游区域土壤重金属污染风险及来源分析

生态功能区在涵养水源、保持水土、维系生物多样性等方面具有重要的作用。本文以位于南岭生态功能区的流域——武水流域为研究对象,采集流域上游交通运输用地、采矿用地、工业用地、耕地及林地5种土地利用类型土壤样品,分析7种重金属Cd、As、Cu、Hg、Ni、Pb、Zn的含量特征,采用内梅罗综合污染指数评价重金属污染的程度,Hakanson潜在生态风险指数法评价土壤重金属潜在生态风险,并应用主成分分析法探究重金属污染的来源。研究结果显示,武水河上游地区土壤重金属Cd、As、Cu、Hg、Ni、Pb、Zn平均含量分别为1.28、72.44、54.62、0.27、68.32、72.29和158.42mg/kg,均高于土壤背景值,其中采矿用地土壤重金含量除Hg外均高于其他类型土壤。均值状态下土壤中Cd和As单因子污染指数分别为5.07、3.25,其中采矿用地中Cd单因子污染指数可达13.59;土壤重金属综合污染指数表明,采矿用地污染最为严重,其次是工业用地,林地呈安全状态。潜在生态危害指数评价结果显示,采矿用地和工业用地达到了强生态危害,其他类型土壤为轻微生态危害,而采矿用地土壤中Cd达到极强生态危害,As为强生态危害。土壤重金属来源研究结果表明,As、Cd、Cu和Zn来源于矿山开采及工业活动,Ni和Hg主要来源于成土母质,Pb则来源于交通运输。研究认为:武水流域上游区土壤重金属污染情况较为严重,Cd和As是区内主要的风险因子,主要来源于矿山开采以及工业活动。