Distribution of Heavy Metals in Near-Shore Sediments of the Swan River Estuary,Western Australia

Estuarine systems adjacent to urban areas are at risk of contamination by contaminants from anthropogenic sources, such as heavy metals. We anticipated that the sediments of the Swan River estuary, which runs through metropolitan Perth in Western Australia, would show metal contamination related to industrialization and inputs of stormwater. Total Cu, Pb and Cd concentrations, and Cu, Pb, Cr and Zn inoperationally-defined fractions, were determined inseparate sampling exercises in near-shore sediments ofthe upper Swan River estuary.Total metal concentrations in sediments were not high (maximum values of 297 mg kg^-1 for Cu, 184 mg kg^-1 for Pb and 0.9 mg kg^-1 for Cd) when compared with Australian environmental assessmentguidelines for soils. On the basis of linear regressions between sediment metal concentrations andphysicochemical properties of the sediments (pH, organic carbon, particle size distribution), no single parameter could explain the variation in metal concentrations for all metals. Sediment organic carbon content was positively correlated with Cu concentration; Cu concentrations also increased significantly with increasing clay content anddecreasing sand content. Pb concentrations showed a significant increase with increasing sediment pH, and were approximately three-fold higher in sediments adjacent to stormwater drain outfalls than in sediments remote from drains; no such effect was observed for Cu or Cd. No effect of distance downstream was observed. Sequential extraction of sediments showed that most of the metals were in relatively immobile forms, for example bound to Feoxides, or only extractable by aqua regia. The enhanced concentrations of Pb near stormwater outfalls suggest that vehicle-derived Pb may be an important contributor of Pb to the estuary.     

Dispersal of Contaminant Metals in the Mining-Affected Danube and Maritsa Drainage Basins, Bulgaria, Eastern Europe

Metal dispersal in the Danube and Maritsa drainage basins resulting from metal mining activities in Bulgaria has been assessed through the collection of 611 samples of river water, river channel and floodplain sediment, and mine waste from over 218 sites. Concentrations of Cd, Cu, Pb, and Zn in river water were found to be highest in close proximity to locations of Cu and Pb–Zn mining regions in the Maritsa catchment. Downstream dispersal of solute metals in these catchments, and into the River Danube, was found to be limited by physical dilution and a well-buffered pH environment. Dispersal of contaminant metals in channel and floodplain sediment was found to be extensive. Contamination was particularly severe in the Rivers Timok and Iskar (Danube catchment) and the Topolnitsa, Chepelarska, and Arda Rivers (Maritsa catchment) and creates the potential of transboundary dispersal of contaminant metals.     

大宝山矿区农田土壤重金属污染及其植物累积特征

对金属矿山选冶活动影响的农田土壤,不同灌溉水源会影响重金属的分布累积特征。根据实际情况将大宝山矿区农田土壤分为污水灌溉区、清水灌溉区、自然修复区和对照区,并进行土壤和植物样品采集,调查研究了土壤的基本理化性质,Cd、Pb、Cu、Zn、Mn 5种重金属的含量和化学形态分布,以及不同区域植物中重金属的含量。结果表明:污灌区Cd、Pb、Cu、Zn的含量最高,是自然修复区和清水灌溉区的1.75倍~10.51倍,对照区最低;Mn在各采样点的含量无显著差别。土壤Cd、Cu、Zn、Pb含量两两之间显著正相关,Mn与Cu、Zn、Cd、Pb呈负相关关系;土壤pH与重金属环境有效态关系密切。残渣态是5种重金属的主要存在形态,有机态含量也较高;Cd的环境有效态含量占总量的比例是其他4种重金属的2倍左右。稻米中5种重金属在清水灌溉区的含量均比污水灌溉区低,其中Cu和Zn的含量在两区域均未超标(NY861-2004),而Pb和Cd的含量严重超标。重金属在自然修复区和清水灌溉区呈现较低的土壤污染和人体健康风险,该研究数据可为金属矿区土壤污染控制提供科学的依据。     

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.     

Regulating the mobility of Cd, Cu and Pb in an acid soil with amendments of phosphogypsum, sugar foam, and phosphoric rock

When acid soil has been contaminated by metals as a result of industrial discharges, accidental spills, or acid mine drainage it may be desirable to retain the metals in the soil rather than allow them to leach away. We have investigated the potential of phosphogypsum (PG), sugar foam (SF), and phosphoric rock (PR) to regulate the availability and mobility of Pb, Cd and Cu. We have also identified changes in attenuation during incubation for 1 year and the effect of aging on metal speciation in amended soils. We studied miscible displacement in columns of undisturbed soil previously treated with solutions of the amendments and soluble metals and, subsequently, single and sequential chemical metal extractions. All amendments increased the soil's metal retention capacity. This, in turn, increased the amount of metal extractable by diethylenetriaminepentaacetic acid (DTPA). However, over time the amounts of DTPA‐extractable metal decreased, particularly for Cu and Pb. Both Cu and Cd were held preferentially within the acetic acid‐extractable fraction (operationally defined exchangeable fraction – EX fraction), whereas Pb was associated mainly with the hydroxylammonium‐extractable fraction (operationally defined bound to Fe and Al hydroxides – OX fraction). Both Pb and Cu in the oxide and organic fractions increased in the PG‐ and SF‐treated soils. In general, the distribution of metal did not change in the PR‐treated columns after the incubation. Finally, scanning electron microscopy in back‐scattered electron mode (SEM–BSE) showed the formation of Al‐hydroxy polymers which provides the soils with additional cation sorption capacity. In the PG‐ and PR‐treated columns, P and S were associated with these formations. The three metals were associated with the Al polymers, probably through direct coordination or the formation of ternary complexes with the inorganic ligands phosphate and sulphate.     

Metal Status of Soils and Plants Irrigated with Water from Lake İznik,Turkey

Lake ?znik, located in the southeast part of the Marmara region in Turkey, is considered the largest lake in the region. Soil pollution from irrigation with lake water has become an important concern for arable lands surrounding the lake. Therefore, a study was conducted to investigate trace element contamination of soils and plants irrigated with water from the lake, which has been polluted with industrial and municipal wastes. Eleven different crops grown in 30 different horticultural fields, consistently irrigated with lake water, were studied. To determine pollutant concentrations, soils, plants, and water were sampled and analyzed for both total and extractable iron (Fe), manganese (Mn), zinc (Zn), copper (Cu), cobalt (Co), nickel (Ni), chromium (Cr), lead (Pb), and cadmium (Cd). Iron, Cu, and Ni in destructively sampled soils were found to be excessive in soils. The results were subjected to statistical analysis using simple correlations and t‐test. There were no statistically significant relationships among the total and extractable metals in soils and extractable plant metals. Because of lack of standard concentrations indicating excessive concentration of extractable elements, statuses of extractable elements in the soils were not evaluated. Cobalt, Pb, Cr, and Cu concentrations were greater than the normal range in leaves. The accumulation of metals differed greatly among the various plant species, but irrigation with lake water did not increase metals in soils. The appearance of metals in soils might be due to agricultural activities and parent material. Continuous monitoring and future studies of the area are recommended to ascertain long‐term impacts of pollution on plants.     

Relationships of Heavy Metals in Natural Lake Waters with Physico-chemical Characteristics of Waters and Different Chemical Fractions of Metals in Sediments

The relationships between heavy metal concentrations and physico-chemical properties of natural lake waters and also with chemical fractions of these metals in lake sediments were investigated in seven natural lakes of Kumaun region of Uttarakhand Province of India during 2003–2004 and 2004–2005. The concentrations of Cr, Mn, Fe, Ni, Cu, Zn, Cd and Pb in waters of different lakes ranged from 0.29–2.39, 10.3–38.3, 431–1407, 1.0–6.6, 5.3–12.1, 12.6–166.3, 0.7–2.7 and 3.9–27.1 μg l^?1 and in sediments 14.3–21.5, 90.1–197.5, 5,265–6,428, 17.7–45.9, 13.4–32.0, 40.0–149.2, 11.1–14.6 and 88.9–167.4 μg g^?1, respectively. The concentrations of all metals except Fe in waters were found well below the notified toxic limits. The concentrations of Cr, Mn, Ni, Cu, Zn, Cd and Pb were positively correlated with pH, electrical conductivity, biological oxygen demand, chemical oxygen demand and alkalinity of waters, but negatively correlated with dissolved oxygen. The concentrations of Cr, Ni, Zn, Cd and Pb in waters were positively correlated with water soluble + exchangeable fraction of these metals in lake sediments. The concentrations of Zn, Cd and Pb in waters were positively correlated with carbonate bound fraction of these metals in lake sediments. Except for Ni, Zn and Cd, the concentrations of rest of the heavy metals in waters were positively correlated with organically bound fraction of these metals in lake sediments. The concentrations of Cr, Mn, Ni, Cu and Zn in waters were positively correlated with reducible fraction of these metals in lake sediments. Except for Cd, the concentrations of rest of the metals in waters were positively correlated with residual fraction and total content of these heavy metals in lake sediments.     

Arsenic and Heavy Metal Uptake and Accumulation in Native Plant Species from Soils Polluted by Mining Activities

Arsenic and heavy metal (specifically Cd, Cr, Cu, Ni, Pb, and Zn) uptake, translocation, and accumulation in ten native plant species spontaneously growing in soils polluted by mining activities were studied, with a focus on future phytoremediation work in polluted soils. Plant and soil samples were collected in the vicinity of the Mónica mine (NW Madrid, Spain). Soil analysis showed the ability of native plants for growing in soils with high concentration levels of Cd, Cu, Pb, Zn, and especially As. From these elements, the highest percentage of extractable elements was found for Cd and the lowest for Pb. A highly significant correlation was observed between total and extractable element concentrations in soils, except for Cu, indicating that total concentration is the most relevant factor for element mobility in these soils. Extractable elements in soils were better correlated with concentrations in plants than total elements in soils; thus, extraction methods applied are suitable to estimate the element phytoavailable fraction in soils, which depends on the plant species and not only on the element mobility in soils. High element concentrations were found in the aboveground parts of Corrigiola telephiifolia (As and Pb), Jasione montana (Cd and Zn), and Digitalis thapsi (As, Cd, Cu, Pb and Zn). However, considering the translocation and accumulation factors, together with the concentration levels found in roots and aboveground parts, only C. telephiifolia could be considered a Pb accumulator and an As hyperaccumulator plant, which could be used for future phytoremediation work in soils polluted with As.     

Total soil heavy‐metal concentrations and mobile fractions after 10 years of biowaste‐compost fertilization

The accumulation of heavy metals (HMs) in soils is the most often cited potential risk of compost application. As the ecological effects of metals are related to mobile fractions rather than to total concentrations in the soil, we measured the total (aqua regia–extractable) HM concentrations, the readily available water‐soluble and the potentially bioavailable LiCl‐extractable fraction of soil HMs in a field experiment after 10 y with total applications of 95, 175, and 255 t ha^–1 biowaste compost (fresh matter). Total soil concentrations of Cd, Cr, Cu, Ni, and Pb in the compost treatments were not significantly higher than in the unfertilized control. Total Zn concentrations increased in the treatment with the highest application rate, as expected from the calculation of the Zn load in the composts. In the mobile fractions, as measured in soil saturation extract and LiCl extract, Cd and Pb were not detectable. Concentrations of Cr, Ni, and Zn were in the range published for unpolluted soils in other studies and did not show any differences according to treatment. Easily exchangeable Cu (in LiCl extract) was increased with compost fertilization, most probably due to complexation with low‐molecular organic complexants. Except for Cd and Zn, the results of the mobile HM fractions in the soil were in good agreement with plant HM concentrations. In conclusion, fertilization with high‐quality biowaste compost at such rates and after 10 y of application gives no cause for concern with regard to both total HM concentrations and available HM fractions.     

Metal accumulation by bermudagrass grown on four diverse soils amended with secondarily treated sewage effluent

Land treatment is increasingly being utilized as a method of waste disposal for both sewage effluent and sludges. While there has been considerable attention directed toward the fate of metallic constituents of sewage sludges, there have been fewer studies of the fate and mobility of metals appled to soils in sewage effluent. This study was undertaken utilizing secondarily treated sewage effluent amended to contain less than 1 mg l^?1 each of Cd, Cu, Ni, Pb, and Zn. The effluent was applied weekly for a period of 1 yr on large undisturbed monoliths of four diverse soils enclosed in lysimeters and sprigged to common bermudagrass (Cynodon dactylon L.). Soil samples were collected periodically and extracted with DTPA to measure plant available metals. Vegetation was harvested, weighed, subsampled and analyzed for total metal content. Total plant uptake of Cd, Cu, Pb, and Ni during the year was less than 1% of that applied. Vegetative uptake of Zn was as high as 2%. Metal uptake was greatest in the soil with the lowest initial pH. Heavy metal concentrations in plant tissue exhibited a cyclic trend. A similar increasing cyclic trend was evident in the DTPA extractable metals in the surface 0 to 12.5 cm of the treated soils. Decreases in plant and DTPA extractable metals occurred when the soils dried, allowing O₂ to enter. Vegetative concentrations of Cd, Cu, and Ni exceeded normal ranges of 0.2 to 0.8, 4 to 15, and 1.0 mg kg^?1, respectively, for vegetation while Pb and Zn were near normal. Only Cd concentration of vegetation posed a threat to grazing animals.     

Reference concentrations for heavy metals in mineral soils, oat, and orchard grass (Dáctylis glomeráta) from three agricultural regions in Norway

Background values for heavy metals are necessary for the assessment of metal pollution of soils and plants. Samples of cultivated and uncultivated soils, oat grain, and seed heads of orchard grass (Dáctylis glomeráta) were collected from central, southeastern, and southwestern Norway. Total and easily extractable concentrations of As, Cd, Cr, Cu, Hg, Ni, Pb, and Zn were determined in soil samples and total concentrations in plant samples. Element distributions have been correlated with petrology of soil parent material, type of mineral deposit, soil depth, geographic area, and land use. Concentrations of heavy metals are generally within the lower part of the normal global range. The petrology of the soil parent material has the greatest influence on aqua regia extracted metal concentrations among the factors studied. DTPA extracted metals show less dependence on rock types. Presence of alum shale results in particularly high values for Cd in both soil extracts and in oat grain. Soil cultivation seems to influence the relative concentration of metals in the topsoil. The ratios of easily extractable to total concentrations of metals are primarily related to the organic matter content. Metal concentrations in oat grain can best be predicted by concentrations in DTPA extracts and soil pH among the factors studied. Seed heads of orchard grass are less affected by concentrations in the soil and appear therefore to be a poor indicator of heavy metals in soils.     

Assessment of soil contamination by potentially toxic elements in the aljustrel mining area in order to implement soil reclamation strategies

Land pollution due to past mining activities is a major environmental issue in many European countries. The Aljustrel mine (SW Portugal), located in the western sector of the Iberian Pyrite Belt (IBP) presents a negative visual and environmental impact as a consequence of the mining activity that has developed since the Roman era. Its impacts are also a restraint on the life quality of the population. The exposure of pyrite and other sulphides to air are responsible for the pollution observed in soils, surface water and stream sediments. This paper investigates the pollution load of potential toxic elements in soil samples collected around the Aljustrel mining area. The aim is to assess the levels of soil contamination with respect to average concentrations of toxic elements in the region and to understand the partitioning and availability of pollutants in the area. The results showed severe soil contamination (mainly As, Cd, Cu, Pb and Zn). The concentrations of As (up to 3936 mg kg⁻¹) and certain heavy metals (up to 5414 mg kg⁻¹ Cu, 61·6 mg kg⁻¹ Cd, 20 000 mg kg⁻¹ Pb and 20 000 mg kg⁻¹ Zn) are two orders of magnitude above the regional South Portuguese Zone (SPZ) background values. The median concentrations of As, Cd, Cu, Pb and Zn exceed the values established for world soils, the European Union, Portugal and Andalusia. The results suggest that the distribution patterns of Co, Cr and Ni element concentrations in the Aljustrel area are primarily influenced by the lithology and geochemistry nature of bedrock. The soil background of this geological domain is characterized by relatively high heavy metal contents, essentially derived from the parent rocks. Copyright © 2010 John Wiley & Sons, Ltd.     

Spatially Explicit Integrated Risk Assessment of Present Soil Concentrations of Cadmium, Lead, Copper and Zinc in The Netherlands

Historic and current agricultural and industrial activities have resulted in accumulation of Cd, Cu, Pb and Zn in soil. To estimate potential risks for ecosystems, agriculture and water quality, an integrated risk assessment was performed for The Netherlands. Risks of metal contamination were assessed on a national scale by comparing present soil concentrations of Cd, Pb, Cu and Zn with critical concentrations of those metals in view of agricultural impacts, ecological impacts and impacts on the quality of groundwater and surface waters. Results show that present soil metal concentrations cause few risks for agriculture or ecosystems; for less than 2% of the surface area present metal levels exceed critical limits. Critical limits for groundwater are only significantly exceeded for Pb (17% of the area), but critical limits for surface water are exceeded throughout the country for Cu and Zn. Taking critical limits used in The Netherlands, the area where exceedances take place is nearly negligible for Cd and low for Pb (less than 3%), but much larger (between 40% and 50%) for both Cu and Zn. Results from this study suggest that accumulation of heavy metals in Dutch soils at present primarily affects the quality of surface waters. This stresses the need for harmonization of soil and water policy. Measures to reduce the load in surface waters to meet target levels, under conditions like those prevailing in The Netherlands, are bound to have an impact on land management.     

Contaminated sediments as a potential source of Zn, Pb, and Cd for a river system in the historical metalliferous ore mining and smelting industry area of South Poland

Background, aim, and scope  Elevated levels of heavy metals in the aquatic and soil systems can be caused by the weathering of mineralized rocks. This enrichment is often considerably enlarged by historical and current mining and smelting activities. In Poland, the most contaminated river systems are those in the Silesia region. The metalliferous ore mining and smelting industries have been the main sources of heavy metal pollutions over the last 100–170 years. The previous and present studies have shown very high concentrations of heavy metals in the bottom sediments of the Mala Panew River, the most polluted tributary of the Oder River. The main objective of this work was to study temporary changes of selected metal (Zn, Pb, and Cd) concentrations in upper layer of bottom sediments at the measuring point near the outlet of the Mala Panew River into the Oder River, and to determine the vertical distribution of the metals in the sediment cores from the most polluted middle part of this river. The mobility of the metals and their potential bioavailability were assessed based on metal partitioning in the sediments and metal concentrations in pore waters. The presented data were compared with metal concentrations in aquatic sediments from similar historical mining and smelting sites in Poland and other countries. Methods  The upper layer of bottom sediment samples from the same Mala Panew River measuring point were collected six times in the period 1997–2005, while five sediment cores were collected once from the middle course of Mala Panew River in 2006. Abiotic parameters such as pH and Eh have been determined in situ. Metal contents were determined in the <20 and <63 μm size fractions of sediments after digestion in a microwave oven with aqua regia or concentrated nitric acid. Metal mobility was assessed in the selected sediment cores by the chemical forms of metals (sequential extraction method) and their concentrations in pore waters were investigated. Results  The concentrations of Cd, Pb, and Zn in the upper layer of sediments varied, depending on both the season and the year of sampling. Their mean concentrations (from six samplings) are [mg/kg]: Zn 1,846, Pb 229 and Cd 73. The metal concentrations in the sediment cores varied with the depth in the range of [mg/kg]: 0.18–559 for Cd, 26.2–3,309 for Pb and 126–11,153 for Zn, although the highest accumulations generally could be observed in the deeper layers. The most mobile metal fractions, i.e., exchangeable, carbonate and easily reducible fractions, are typical of Zn and Cd. Cadmium was found to be the most mobile metal and its relative contribution ranges from 84 to 96%, while in the case of Zn it ranged from 45 to 94%. Lead is mainly associated with the moderately reducible fraction (30–60%). Relative contributions of metal chemical forms slightly vary with the depth in the sediment profile. The results obtained for the pore water samples show very high concentrations of the metals studied, especially in the case of Cd (31–960 μg/dm³) and Zn (300–4,400 μg/dm³). Discussion  Accumulation of Cd, Pb, and Zn in the upper layer of the bottom sediments and in the sediment core samples from the Mala Panew River is very high, considerably exceeding the local geochemical background. High contributions of mobile Cd and Zn and the toxicity of cadmium can cause environmental risk. Our measurements also suggest that mobile metals can migrate into groundwater, whereas the groundwater itself can leach some chemicals from river sediments, because of a relatively high water table in the study area, especially during rainfall periods. Comparison of the results obtained with the literature data from the last decade shows that the concentrations of Cd and Zn in the sediments from the Mala Panew River are the highest among other submersed sediments in Poland and other regions (e.g., the Mulde River, Germany). Conclusions  The Mala Panew River is one of the most polluted rivers when compared with similar historical mining and smelting areas in Poland and elsewhere. The sediments studied are strongly polluted with the metals analyzed. In the upper layer of the bottom sediments there has been no reduction of Zn and Cd amounts over the last decade, which could suggests a long-term migration and a secondary contamination. Considerably higher accumulations of metals in overbank sediment cores and in the deeper core section could result from strong contamination in previous decades and translocation of Cd and Zn (secondary pollutants). The relatively high concentrations of the two metals in pore waters support these findings. Cadmium is crucial in the environmental risk assessment because of its high mobility and toxicity. These data are important for water/sediment management in the transboundary Oder River catchment, situated in Poland, Germany and the Czech Republic. Recommendations and perspectives  It is important to assess mobility phase and pore water in the contaminated historical aquatic sediments. Such studies may help explain the changes, which take place in the sediment layers as well as at the water–sediment interface. Obtained results should be used for the risk assessment of the historical contaminated sediments at the local river-basin scale. The treatment of contaminated sediments, e.g., dragging activity, should be considered as very important in management strategies in order to avoid remobilization of metals.     

Estimation of Source of Heavy Metal Contamination in Sediments of Gomti River (India) using Principal Component Analysis

This study explores the extent and possible sources of heavy metal (Cd, Cr, Cu, Fe, Mn, Pb, Zn and Ni) contamination in the bed sediments of the Gomti River performing principal component analysis on the five years (Jan. 1994–Dec. 1998) data set obtained through continuous monitoring of the river water and bed sediments at eight selected sites and water/wastewater of its tributaries/drains. Influence of anthropogenic activities on metal contamination of the bed sediments was evaluated through computing the geoaccumulation index for various metals at studied sites. PCA performed on combined (river bed sediment, water, suspended solids, water/wastewater from tributaries/drains) data set extracted two significant factors explaining more than 58% of total variance. Factor loadings suggested the presence of both natural as well as anthropogenic sources for all these metals in the river bed sediments. Among all the sites, the sites 4 and 5 are more contaminated with Cd, Cu, Cr and Pb, which was supported by the geoaccumulation indices computed for metals. Factor scores revealed presence of seasonal (monsoon-related) differences in metals profiles for river water and suspended solids and absence of seasonal differences for bed sediment and wastewater. Further, the metal contamination of the bed sediment was also evaluated using biological thresholds. Results suggested that the river bed sediments are contaminated with heavy metals, which may contribute to sediment toxicity to the freshwater ecosystem of the Gomti River.     

Extractability and plant uptake of heavy metals in alum shale soils

Abstract

Fifty soil samples (0–20 cm) with corresponding numbers of grain, potatoes, cabbage, and cauliflower crops were collected from soils developed on alum shale materials in Southeastern Norway to investigate the availability of [cadmium (Cd), copper (Cu), zinc (Zn), lead (Pb), nickel (Ni), and manganese (Mn)] in the soil and the uptake of the metals by these crops. Both total (aqua regia soluble) and extractable [ammonium nitrate (NH₄NO₃) and DTPA] concentrations of metals in the soils were studied. The total concentration of all the heavy metals in the soils were higher compared to other soils found in this region. Forty‐four percent of the soil samples had higher Cd concentration than the limit for application of sewage sludge, whereas the corresponding values for Ni, Cu, and Zn were 60%, 38%, and 16%, respectively. About 70% the soil samples had a too high concentration of one or more of the heavy metals in relation to the limit for application of sewage sludge. Cadmium was the most soluble of the heavy metals, implying that it is more bioavailable than the other non‐essential metals, Pb and Ni. The total (aqua regia soluble) concentrations of Cd, Cu, Zn, and Ni and the concentrations of DTPA‐extractable Cd and Ni were significantly higher in the loam soils than in the sandy loam soils. The amount of NH₄NCyextractable metals did not differ between the texture classes. The concentrations of DTPA‐extractable metals were positively and significantly correlated with the total concentrations of the same metals. Ammonium nitrate‐extractable metals, on the other hand, were not related to their total concentrations, but they were negatively and significantly correlated to soil pH. The average concentration of Cd (0.1 mg kg^‐1 d.w.) in the plants was relatively high compared to the concentration previously found in plants grown on the other soils. The concentrations of the other heavy metals Cu, Zn, Mn, Ni, and Pb in the plants were considered to be within the normal range, except for some samples with relatively high concentrations of Ni and Mn (0–11.1 and 3.5 to 167 mg kg‘¹ d.w., respectively). The concentrations of Cd, Cu, Zn, Ni, and Mn in grain were positively correlated to the concentrations of these respective metals in the soil extracted by NH₄NO₃. The plant concentrations were negatively correlated to pH. The DTPA‐extractable levels were not correlated with plant concentration and hence DTPA would not be a good extractant for determining plant availability in these soils.     

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.     

Use of Drinking Water Treatment Residuals in Reducing Bioavailability of Metals in Biosolid-Amended Alkaline Soils

This greenhouse study evaluated the use of drinking-water-treatment residuals (WTRs) to reduce the bioavailability of metals in the biosolid-amended agricultural alkaline soils. Results showed that increasing the application rate of biosolids increased the accumulation of lead (Pb), nickel (Ni), copper (Cu), and cadmium (Cd) in corn (Zea mays cv. single hybride 10), with greater metal concentrations in roots than in shoots. However, the addition of WTRs (1–4%, w/w) to the soil amended with 3% biosolids significantly (P < 0.05) decreased the concentrations of soil diethylenetriaminepentaacetic acid (DTPA)–extractable metals. The accumulation of Pb, Ni, Cu, and Cd in corn significantly correlated with the DTPA-extractable metal concentrations in the soils. Plant metal concentrations were significantly affected by the soil type, application rates of biosolids and WTRs, and the ratio of WTRs to biosolids in the soils. The 1:1 application ratio of WTRs to biosolids at the 3% application rate effectively reduced the accumulation of metals in corn tissues.     

工业型城乡交错区农业土壤Cu、Zn、Pb和Cd的空间分布及影响因素研究

在江苏省无锡市工业型城乡交错区，选择8km2区域，采集119个土壤样品，对土壤Cu、Zn、Pb,Cd及其有效态含量的空间分布和影响因素进行探讨。结果表明：该区土壤Cu、Zn、Pb、Cd含量和变异系数都明显增加，土壤有效态重金属含量与相应的全量重金属含量具有显著相关性。土壤Cu、Zn、Cd空间变异主要受到工业影响，但由于该区工业类型的多样性和工厂分布的分散性，Cu、Zn、、Cd空间分布模式并不相同。本区土壤Pb的分布与工厂分布的相关性不大，但随与城市距离增加而降低。公路和土地利用与土壤重金属含量的关系表现不明显。该区工业污染对土壤重金属空间变异的影响可能掩盖了公路和土地利用等的影响，建议在城乡交错区合理安排工业布局以控制土壤受重金属污染的范围。