Trace elements in surface soils from the mineralized area of Madison County, Missouri, U.S.A.

Duplicate, bulked surface soil samples, from sites 10m apart, were collected at 97 locations 1000 m apart on a regular grid measuring 8x11 km. Data were obtained for Ag, Ba, Be, Cd, Co, Cr, Cu, Li, Mn, Ni, Pb, V and Zn. One field sample was a good predictor of its nearby duplicate for Co, Cu, Ni and Pb, satisfactory for Ba, Be, Cr, Mn and Zn, but poorer for Cr, Li and V. Maps of the variation in precision of the field samples did not reveal any association between abandoned mine sites and high variability. The median coefficient of variation for trace elements in the field duplicates was between 8 and 19.5%. The duplicated field data were averaged to yield a mean soil metal concentration at each sample location. Concentrations of Ba, Be, Cr, Li, Sr and V were comparable with other published values for similar soils in Missouri. Concentrations of Co, Cu, Mn, Ni, Pb and Zn were higher which was explained by pollution from mining activities. A graphical technique was used to calculate background levels for metals in the second group. Samples of forest litter were collected at 12 locations: Ag, Ba, Cd, Mn, Sr and Zn concentrations were higher in the litter whereas Li and V concentrations were higher in the subjacent mineral soil. Computer isoline maps of the distribution of elements revealed an association between areas of high soil Cu, Co, Ni, Pb and Zn and abandoned mines or mineralized rocks.     

土壤可见光-近红外反射光谱与重金属含量之间的相关性

发展基于反射光谱技术的快速、简便、低成本的土壤重金属信息提取方法是区域土壤重金属污染治理所需要的。选择江西贵溪铜冶炼厂污染区,分析了9种重金属元素(Cu、Pb、Zn、Cd、Co、Ni、Fe、Mn及Cr)与土壤可见光-近红外反射光谱之间的相关性及其相关的原因。研究表明,研究区土壤中存在Cu(含量介于66.71~387 mg kg-1之间)和Cd(含量介于0.36~6.019 mg kg-1之间)的强烈富集。土壤重金属含量与反射光谱之间存在显著相关,污染元素Cu的最高相关系数为-0.87,Pb、Zn、Co、Ni、Fe的最高相关系数达到高度相关(|r|>0.80),Cr、Cd、Mn的最高相关系数达到显著相关(|r|>0.70)。微分光谱适于获取土壤中的重金属元素信息,利用组合波段能显著提高相关性。Cu与反射光谱之间的相关性主要受有机质的影响;Pb、Zn、Co、Ni主要受黏土矿物和铁锰氧化物的影响;Cr与反射光谱之间的相关性同时受有机质和黏土矿物的影响。     

新乡市大棚菜田土壤重金属积累特征及污染评价

采用微波消解-ICP-AES技术,测定不同种植年限大棚菜田土壤样品中As、Pb、Zn、Cd、Cr、Mn、Ni、Cu等重金属的含量,研究不同种植年限与大棚菜田土壤重金属累积的相关性以及大棚菜田土壤重金属累积特征,并利用地积累指数法进行污染评价。结果表明:大棚菜田土壤重金属Zn、Pb、Ni、Mn和Cu的含量与种植年限具有极显著相关性;大棚菜田土壤中重金属Cd和Cr的含量与种植年限不相关。重金属元素间相关性分析表明,Zn与Pb、Cd、Ni、Mn、Cr、Cu,Pb与Cd、Ni、Mn、Cr、Cu,Cd与Ni、Mn、Cr,Ni与Mn、Cr、Cu,Mn与Cr、Cu具有污染同源性,Cu与Cd、Cr不具有污染同源性。地积累指数法污染评价结果显示Cd的污染等级达到了6级,已构成了极严重污染;Zn和Cu的污染等级达到2级,已构成了中度污染;Pb、Mn的污染等级达到1级,已经构成了轻~中度污染;As、Ni、Cr均未构成污染。     

博斯腾湖湿地边缘带农田土壤重金属的污染风险评价

对新疆博斯腾湖湿地边缘带农田土壤中8种重金属元素(As、Cd、Cr、Cu、Mn、Ni、Pb和Zn)地球化学特征进行分析。采用污染负荷指数(PLI)、潜在生态风险指数(RI)和生态风险预警指数(IER)对农田土壤重金属污染与环境风险进行评价。结果表明:(1)湿地边缘带农田土壤Pb和Zn呈现重度污染,As、Cd、Cr和Ni轻度污染,Cu轻微污染,Mn无污染。土壤As、Cd、Cr、Cu、Ni、Pb和Zn平均含量处于轻微风险水平。Cd是污染程度与生态风险等级最高的重金属元素;(2)湿地边缘带农田土壤PLI平均值为1.43,呈现轻度污染,RI平均值为20.62,呈现轻微生态风险状态,IER的平均值为–4.53,呈现无警态势。湿地边缘带PLI、RI与IER空间分布格局基本一致;(3)湿地边缘带农田土壤Pb与Zn来源主要受到人类活动的影响,Cr、Cu、Mn与Ni来源主要受到土壤地球化学作用的控制,As与Cd受自然因素和人为因素共同影响。     

Spatial distribution of soil heavy metal concentrations as indicator of pollution sources at Mount Križna (Great Fatra,central Slovakia)

The objective of this study was to test the suitability of a simple approach to identify the direction from where airborne heavy metals reach the study area as indication of their sources. We examined the distribution of heavy metals in soil profiles and along differently exposed transects. Samples were taken from 10 soils derived from the same parent material along N-, S-, and SE-exposed transects at 0—10, 10—20, and 20—40 cm depth and analyzed for total Al, Cd, Cr, Cu, Fe, Mn, Ni, Pb, and Zn concentrations. The heavy metal concentrations at 0—10 cm were larger than background concentrations in German arable soils except for Cr (Cd: 0.6—1.8 mg kg^—1; Cr: 39—67; Cu: 40—77; Ni: 87—156; Pb: 48—94; Zn: 71—129; Fe: 26—34 g kg^—1; Mn: 1.1—2.4). Decreasing Cd, Cu, Mn, and Pb concentrations with increasing soil depth pointed at atmospheric inputs. Aluminum and Ni concentrations increased with soil depth. Those of Fe, Cr, and Zn did not change with depth indicating that inputs at most equalled leaching losses. The Pb accumulation in the surface layer (i.e. the ratio between the Pb concentrations at 0—10 to those at 20—40 cm depth) was most pronounced at N-exposed sites; Pb obviously reached Mount Križna mainly by long-range transport from N where several industrial agglomerations are located. Substantial Cd, Cu, and Mn accumulations at the S- and SE-exposed sites indicated local sources such as mining near to the study area which probably are also the reason for slight Cr and Zn accumulations in the SE-exposed soils. Based on a principal component analysis of the total concentrations in the topsoils four metal groups may be distinguished: 1. Cr, Ni, Zn; 2. Mn, Cd; 3. Pb (positive loading), Cu (negative loading); 4. Al, Fe, indicating common sources and distribution patterns. The results demonstrate that the spatial distribution of soil heavy metal concentrations can be used as indication of the location of pollution sources.     

Increasing the Knowledge of Heavy Metal Contents and Sources in Agricultural Soils of the European Mediterranean Region

This paper contributes to increase the knowledge of the contents and sources of heavy metals (Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb and Zn) to agricultural soils in Castellón province (Spain), a representative area of the European Mediterranean region. The surface horizons of 77 agricultural soils under vegetable crops were sampled and heavy metals were analysed by atomic absorption spectroscopy (AAS) after microwave extraction using the USEPA 3051A method. Mean heavy metal contents were similar to those obtained in other areas of this region. However, heavy metal contents (e.g. Cr, Pb) in some soils were above the maximum limit set in the 86/278/CEE Directive. Multivariate analysis (correlation analysis and principal component analysis – PCA) was performed so as to identify the sources of heavy metals to soils. Co, Fe and Ni were highly correlated amongst them (r?>?0.800; p?<?0.01), whereas Cr and Mn were less correlated with Co, Fe and Ni (r?>?0.500; p?<?0.01). Other relationships among heavy metals (i.e. Cu, Pb and Zn) were also identified, although correlation coefficients were not so high as those among Co, Fe and Ni (r?<?0.500; p?<?0.01). Contents of Co, Fe, Mn and Ni were interpreted to be mainly associated with parent rocks corresponding to the first principal component (PC1). On the other hand, Cd, Cu, Pb and Zn were interpreted to be mainly related to anthropogenic activities and comprised the second (Pb and Zn) and the third (Cd and Cu) principal components (PC2 and PC3, respectively), designated as anthropogenic components. Remarkably, Cr appears to be related in the study area to both the lithogenic and the anthropogenic components. Lithogenic elements were highly correlated with soil properties. Positive relationships with CEC (r?>?0.200; p?<?0.05) and clay (r?>?0.400; p?<?0.01), and negative relationships with carbonates (r?>??0.400; p?<?0.01) and sand (r?>??0.300; p?<?0.01) were observed. Anthropogenic elements were less correlated with soils properties, since these elements are generally more mobile because they form more soluble chemical species associated to anthropogenic sources. Particularly, no correlation was found between Cd and Zn and soil properties. These findings extend results achieved in other parts of the region, highlighting the need to set soil quality standards in order to declare soils affected by anthropogenic pollution, particularly in the case of anthropogenic metals such as Cd, Cu and Pb, and also Cr and Zn in some areas. Further knowledge from other areas in this region would improve the basis for proposing such standards at regional level, which is a priority objective in Europe according to the European Thematic Strategy for Soil Protection.     

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.     

山东省沂源县土壤重金属来源分布及风险评价

为建设高标准农田及保证食品安全,对土壤重金属污染状况进行精确评估极为关键。选取山东省山地丘陵区典型区域—沂源县为研究区,系统采集427个表层土壤样品(0~20 cm),测定了As、Cd、Co、Cr、Cu、Mn、Ni、Pb、Hg和Zn共10种重金属含量;采用多元统计分析和地统计分析方法,揭示了土壤重金属的主要来源;进一步分析得出研究区重金属的空间分布以及与成土母质、工业排放和农业生产污染之间的关系。研究表明:1)沂源县表层土壤中10种重金属元素的平均含量值均高于土壤背景值但未超过国家二级土壤元素限定值,存在一定程度的重金属富集。2)经主成分分析和单因素方差分析后将研究区重金属的来源主要分为3类:As、Co、Cu和Mn主要来源于成土母质,属自然源因子;Hg、Cd、Zn和Pb受到母质和工农业污染双重控制,属于混合来源;Cr和Ni主要是成土母质影响下的自然来源。3)自然来源重金属含量的高值区主要与石灰岩成土母质类型分布相一致,Hg、Cd、Zn和Pb元素含量的高值区与工业区分布基本一致。4)通过潜在生态风险评价,沂源县表层土壤目前处于中度潜在生态风险等级,其中Hg和Cd潜在生态风险最强,达到中度生态危害,其他元素具有轻微的潜在生态危害。研究中通过多元统计-地统计模拟分析法有效的揭示了土壤重金属污染源汇特征,可作为评估该区土壤污染现状和对土壤重金属污染进行风险评价的重要依据。     

Influence of graded EDTA applications on mobilization and translocation of trace elements—a soil column experiment

Increasing concerns about potential environmental effects of ethylenediaminetetraacetic acid (EDTA) accumulation in soils require better understanding of its behavior and its effect on trace element mobilization. In this study we investigated the effect of EDTA on soil trace element mobilization in undisturbed soil columns taken from a heavy metal contaminated field. The columns were leached by EDTA solutions of different concentrations under unsaturated, steady‐state conditions. The transport of trace elements (Cd, Co, Cr, Cu, Fe, Mn, Mo, Ni, Pb, Sn, Zn) and EDTA was monitored by regularly collecting the leachates. After the termination of the leaching experiment the soil columns were divided into 5 layers to determine trace elements and EDTA concentrations in the soil. The results revealed that the soil analysis alone was not suitable to infer mobilization or immobilization patterns in relation to the EDTA concentration, as the mobilized fraction was too small in relation to the total trace metal concentrations in the soil. Analysis of the leachates displayed that after 2–4 pore volumes the EDTA output concentration reached about 80% of the input concentration. The trace element concentrations in the leachates showed that some elements were mobilized by EDTA (Cd, Cu, Fe, Pb, Co, Ni, Zn) while others were immobilized (Mn, Cr, Mo, Sn) in the soil columns after EDTA application.     

Heavy metal contamination of soils in Northern Slovakia

Environmental damages like forest decline in Northern Slovakia could be a result of long-distance transport of pollutants with the dominating north-west winds. On 10 sites, primarily in the northbound upper slopes of west-east oriented mountain ranges in Northern Slovakia, the extent of the heavy metal contamination in soils along a north-south transect was examined. Oi, Oe, Oa, A, and B horizons were sampled and the total concentrations of Al, Cd, Cr, Cu, Fe, Mn, Ni, Pb, and Zn were determined. The ranges of heavy metal concentrations in the forest floor were higher than reported for comparable samples from Bavarian soils except for Zn (Cd: 0.65–1.77; Cr: 12–40; Cu: 19–41; Ni: 8–24; Pb: 70–187; Zn: 31–92 mg kg^?1), in the mineral soil the concentrations were lower. The depth distribution of the metal concentrations indicated a contamination with Cd, Cr, Cu, Ni, Pb, and Zn. The concentration differences between forest floor and mineral soil tended to be higher at the northern than at the southern sites for Cu, Ni, Pb, and Zn, indicating a long-distance transport from the north. Correlation and principal component analyses of the total metal concentrations revealed three groups: Cu, Pb, and Zn inputs mainly seemed to result from long-distance transport from the north, Cr and Ni inputs additionally from local sources. Cd probably had its origin mainly in local sources. This result was further confirmed by the grouping of the sites when clustered.     

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.     

北京市密云水库上游金矿区土壤重金属含量、来源及污染评价

运用多变量分析、富集因子及地累积指数法对北京市密云水库上游金矿区土壤重金属的来源、污染评价进行了研究。利用电感耦合等离子体质谱法（ICP—MS）测定土壤中Be、V、co、Ni、cu、cd、Pb的含量,用原子荧光光谱法（AFS）测定As、Hg含量,用X射线衍射（xRD）测定土壤所含矿物质成分。结果表明,除As外各重金属平均含量均高于北京市土壤元素背景值。XRD分析结果显示,土壤的矿物质成分相似,主要包括石英、长石、伊利石、高岭石、蒙脱石、方解石。多变量分析（主成分、聚类、相关性分析）表明,cu、cd、Pb和Hg为人为源,主要来源于矿产的开采或运输过程;Be、V、Ni和co来自混合源,即矿产开采过程和土壤背景;As为自然源,来自于岩石矿物的风化、侵蚀及土壤母质。富集因子法及地累积指数法评价结果表明,cu、Cd、Pb、Hg污染较严重,受人为活动的显著影响,而Be、V、co、Ni轻微污染,As无污染。该结果进一步验证了多变量分析的结果。     

太原市污灌区土壤重金属污染现状评价

对太原市污灌区土壤重金属分布特征进行了分析评价,结果表明重金属Pb、Zn、Cu、Ni、Mn、Cr、As、Hg、Cd含量均值均未超过土壤环境质量标准（GB15618—1995）,但其平均值均显著高于太原市土壤背景值。各重金属间的相关分析表明,Pb、Zn、Cu、Ni、Mn、Cr、As、Cd之间呈极显著相关,说明这8种元素污染源可能相同。Hg是本区表层土壤重金属污染的主要因子,重金属元素的污染程度依次为Hg〉Cd〉Pb〉As〉Cu〉Zn〉Cr〉Mn〉Ni。土壤重金属单项污染指数均值均大于1,综合污染指数为2.81,总体上,污染水平为中度及其以上。各种重金属单因子污染指数和综合指数在研究区有相似的空间分布格局,总体分布趋势为东南部小店地区和中南部晋源区相对较高,南部清徐县相对较小;通过因子分析并结合污灌区污染源调查,表明Hg除受污水灌溉的影响外,燃煤释放的Hg可能是重要来源之一,Cd、Zn、Pb和Cu可能来自污水灌溉和大气沉降,以污水灌溉的贡献为主,Ni、Mn、As、Cr来自污水灌溉。Hg、Cd是太原市污灌区土壤中需要优先控制的重金属。     

宝鸡长青镇铅锌冶炼厂周边土壤重金属污染研究

通过野外采样和实验室分析,在分析土壤基本理化性质的基础上,重点研究宝鸡长青镇铅锌冶炼厂周边土壤中重金属元素的含量和形态特征,并进行了污染评价。结果表明,宝鸡长青镇铅锌冶炼厂周边土壤中Cu、Pb、Zn、Mn、Co、Ni、Cr的平均含量分别为31.8、41.3、102.6、704.6、14.4、37.4、83.2mg·kg-1,均高于陕西省和全国土壤元素背景值,尤其是Cu、Pb和Zn。土壤中Cu、Zn、Ni和Cr主要以残余态的形式存在,Pb、Mn和Co主要以可还原态和残余态的形式存在,重金属的迁移顺序为Mn（63.91%）〉Pb（60.08%）〉Co（51.70%）〉N（i37.12%）〉Zn（32.09%）〉C（r30.58%）〉Cu（19.95%）,其中,Mn、Pb和Co有50%~65%可以发生迁移,易被生物体利用,危害较大。评价结果表明,宝鸡长青镇铅锌冶炼厂周边土壤主要受到了Pb的轻度污染。     

Pollution and Ecological Risk Assessment of Heavy Metals in Farmland Soils in Yanqi County,Xinjiang, Northwest China

A total of 50 farmland soil samples were collected from the Yanqi County, Xinjiang, China, and the concentrations of eight heavy metal elements (As, Cd, Cr, Cu, Mn, Ni, Pb and Zn) were determined by standard methods. The spatial distribution, pollution level and ecological risk status of heavy metals were analyzed based on GIS technology, the Geo-accumulation Index (Igeo), the Pollution Load Index (PLI) and the Potential Ecological Risk Index (RI). Results indicated that: (1) The average contents of Cd, Cr, Ni, Pb, and Zn of farmland soils exceeded the background values of irrigation soils in Xinjiang by 1.5, 1.40, 1.33, 2.63, and 4.92 times, respectively. Cd showed a no-pollution level, Zn showed a partially moderate pollution level, Pb showed a slight pollution level, and Cr, Cu, As, Mn, and Ni showed no-pollution level, compared to the classification standard. The PLI values of heavy metal elements of farmland soils varied from 0.83 to 1.89, with an average value of 1.29, at the moderate pollution level. (2) The Individual Potential Ecological Risk Index for heavy metals in the study area was ranked in the order of: As > Ni > Cu > Cd > Pb > Cr> Zn. The RI values of heavy metals of farmland soils varied from 3.45 to 11.34, with an average value of 6.13, at the low ecological risk level. (3) Cu and Mn of farmland soils were mainly originated from the soil parent material and topography of the study area. As, Cd, Ni and Pb were mainly originated from human activities, and Cr and Zn may originated from both natural and anthropogenic factors in the study area.     

Heavy Metals, Phosphorus and Some Other Elements in UrbanSoils of Hangzhou City, China

Health implications of inhaling and/or ingesting dust particles with high concentrations of heavy metals from urbansoils 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 82locations in Hangzhou City were measured to:a) assess their distribution in urban environments;and b) understand theirdifferentiation as related to land use. Metal mobility was also studied using a three-step sequential chemical fractionationprocedure. 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 commercialand industrial areas, most samples had metal concentrations below their allowable limits. Statistical analyses revealedthat the 16 measured elements in urban soils could be divided into four groups based on natural or anthropic sourcesusing a hierarchical cluster analysis. Additionally, Cu, Pb, and P showed similar spatial distributions with significantpollution 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 werethe main sources of these seven metals. Moreover, the data highlighted land-use as a major influence on heavy metalconcentrations and forms found in topsoils with large proportions of soil Cd, Co, Cr, and Ni found in residual fractionsand soil Cu, Pb and Zn mainly as extractable fractions.     

Wet Deposition of Trace Metals in Singapore

The concentrations of 12 trace metals (Al, Cd, Cr, Cu, Co, Fe,Mn, Ni, Pb, Zn, V, and Ti) in wet depositions are reported. Eighty four rainwater samples were collected using an automated wet-only sampler in Singapore for one year (2000) and subjected to chemical analysis using ICP-MS. Based on the volume-weighted meanconcentrations measured, the trace metals were classified into three groups: Al and Fe with an average concentration of largerthan 15 μg L^-1, Cr, Cu, Mn, Ni, Pb, Zn, V, and Ti withconcentrations between 1 and 10 μg L^-1, and finally Co and Cd with concentrations lower than 1 μg L^-1. Elementenrichment factors were calculated to distinguish between naturaland anthropogenic sources. The calculation of crustal enrichmentfactors with Al as the reference element indicated that while Ti,Fe and Mn originated from crustal sources, the remaining trace metals (Cd, Cr, Co, Cu, Ni, Pb, Zn and V) were mainly derived from anthropogenic sources. The removal of the trace metals from the atmosphere by precipitation was influenced by the rainfall amount as well as pH. The magnitude of the measured average annual wet deposition fluxes of Al, Fe, and combustion-generatedelements such as V, Ni, and Cu is higher than that reportedfor other sites outside Singapore, owing to abundant rainfallthroughout the year in this region.     

Die räumliche Variabilität von Schwermetall-Konzentrationen in Niederschlägen und Sickerwasser von Waldstandorten des Sollings

Local variability in the heavy metal concentrations of precipitation and seepage water from forest sites in the Solling Concentrations of Cr, Mn, Fe, Co, Ni, Cu, Zn, Cd and Pb in precipitation and seepage water have been measured continuously with local replicates during a 6-months period at a beech and a spruce forest site. Variation coefficients of the avarage concentrations were, in most cases, well below 30 %, being mainly caused by local differences. Comparison of means showed a significant increase of heavy metal concentration in the canopy drip of beech (Mn, Fe, Pb) and spruce (Cr, Mn, Fe, Ni, Zn, Pb) compared to bulk precipitation measured in the open field. Concentration of Mn, Co, Ni, Zn and Cd in the seepage water is significantly higher under spruce compared to beech. These results point at higher filter efficiency of the spruce canopy, compared with beech, for air pollutants, but a smaller retention capacity of the soil under spruce for heavy metals.     

包头市铜厂周边土壤中重金属垂直分布特征与形态分析

为了解包头市铜厂周边地区土壤剖面中重金属污染状况,采用火焰原子吸收分光光度法和Tessier连续提取法,对土壤中6种重金属（Cu,Zn,Mn,Ni,Pb和Cd）的垂直分布特征、形态及潜在生物可利用性进行了分析。结果表明:研究区土壤剖面各层土壤中6种重金属含量均超过内蒙古土壤背景值,Cu,Pb和Cd为主要污染物。随采样深度的增加,Cu,Zn,Pb和Mn的含量呈现下降趋势,且由相关性系数可知重金属Cu,Zn和Pb可能有相同人为或自然污染源;土壤剖面中6种重金属均主要以残渣态存在,含量均在50%以上,对生物危害较小;潜在生物可利用性分析结果为:Cu（32.61%） > Mn（31.85%） > Ni（24.90%） > Zn（16.60%） > Cd（15.23%） > Pb（14.87%）,Cu和Mn的潜在生物可利用性较大,其次为Ni,Zn,Cd和Pb潜在生物可利用性较小。     

Distribution of 32 Elements in Organic Surface Soils: Contributions from Atmospheric Transport of Pollutants and Natural Sources

Data are presented for 32 elements (Li, Be, B, Ti, V, Cr, Mn, Co, Ni, Cu, Zn, Ge, As, Rb, Sr, Y, Zr, Mo, Ag, Cd, Sb, Cs, Ba, La, Ce, Pr, Nd, Sm, Hf, Tl, Pb, Bi) in organic-rich surface soils in Norway, based on samples from 464 sites. By considering geographical distributions based on isopleths, results from factor analysis, and ANOVA of median values from 12 different geographical regions, the contributions from natural and anthropogenic sources are estimated for each element. Long-range atmospheric transport of pollutants from areas out of Norway is a dominant source for Cd, Sb, Pb, and Bi and also a strongly contributing factor for Zn, As, Mo, and Tl. Also V, Ni, Cu, and Ge are somewhat affected, but other factors dominate for these elements. Local point sources of pollution provide significant contributions to soil concentrations of Ni, Cu, Zn, As, Mo, and Cd. The local bedrock is the overriding source of Li, Be, Ti, V, Cr, Mn, Rb, Zr, Cs, Ba, REE, Hf, and probably of Ge and Ag. Surface enrichment by root uptake in plants and return to the soil surface by decaying plant material is particularly evident for Mn, Zn, Rb, Cs, and Ba. These elements show no clear difference between south and north in the country, indicating that their plant uptake does not depend on latitude. In the case of B and Sr, atmospheric deposition of marine aerosols is an important source. Rb and Ag, and to a less extent Mn, Ga, and Ba, appear to be depleted in soils near the coast presumably due to cation exchange with airborne marine cations.