Trace element distributions in surficial sediments of the northern Tyrrhenian Sea: Contribution to heavy-metal pollution assessment

The trace element distributions in surficial sediment of Tyrrhenian Sea have been investigated as a part of a series of studies on the environmental quality of the area off the Tuscany coast (west-central Italy). This research has focused on the presence of possible contaminated zones; it also provides data for the identification and future monitoring and control of pollution sources. The study of numerous surface sediments and core samples has made it possible to distinguish between heavy-metal enrichments related to natural sources and other anomalies caused by anthropogenic contamination. Over much of the basin, the surface Pb, Cu, Zn, and As contents appear considerably enriched relative to those below 15 cm; among these metals, Pb shows the highest and most widespread enrichment. Only in the case of some coarse-grained sediments close to the mouth of Cecina River it is possible to relate anomalously high Zn contents to natural sources. In all other sampling stations, the enrichments of Pb, Cu, Zn, and As are ascribed to man's influence. The sediment distributions of Co, Cr, and Ni do not seem to be related to anthropogenic activities; rather they mirror influx of materials derived from sources of ophiolitic rock. The distribution of barium shows only two significant positive anomalies, and both are related to natural causes. Concentrations of vanadium are high in a zone close to an important smelting plant; these are thought to be of anthropogenic origin.     

The chemical and physical characteristics of heavy metals in humus and till in the vicinity of the base metal smelter at Flin Flon, Manitoba, Canada

 Trace element geochemistry of humus (<0.425 mm) and till (<0.002 mm) collected in the Flin Flon-Snow Lake area, northern Manitoba and Saskatchewan, provides a regional context for assessing smelter contamination in the environment. The area includes a Cu-Zn smelter known to discharge As, Cd, Cu, Fe, Hg, Pb, and Zn. In this study, sequential extraction analyses, scanning electron microscopy and x-ray diffraction analyses were used on a suite of samples to determine: (1) the chemical and physical characteristics of heavy metals in surficial sediments related to distance from the smelter, (2) criteria for assessing the relative contribution of these metals from natural and anthropogenic sources, and (3) the potential of these metals for remobilization in the environment. Humus geochemistry reflects the anthropogenic and natural component of heavy metal concentrations. Smelter-related elements show anomalously high values adjacent to the smelter, decreasing with distance until background values are reached at 70–104 km, depending on the element. In humus, Zn is associated primarily with labile phases; Hg with non-labile phases. Adjacent to the smelter, high proportions and concentrations of Zn and Hg in non-labile phases, indicative of smelter-derived particulates, are confirmed by SEM examination. The particles occur as spheres, irregular grains, and with organics. With increasing distance from the smelter, the geochemical response to bedrock composition is more obvious than the anthropogenic input. Till geochemistry reflects the natural variation imposed by bedrock composition. At highly contaminated sites (<3 km from the smelter), increased percentages of smelter-related elements in labile phases suggests heavy metals are leached from humus to the underlying sediment. Received: 5 November 1996 · Accepted: 31 March 1997     

Atmospheric trace metals: global cycles and assessment of man's impact

Global data are presented for sources of atmospheric input for 20 trace metals, and the relative importance of natural and anthropogenic sources is assessed. Interference factors are calculated as (total anthropogenic emissions/total natural emissions) × 100. For lithophile metals such as Fe and Mn, interference factors are small. In contrast, the atmophile metals, such as As, Se and Hg, exhibit large interference factors. A significant degree of correlation exists between interference factors and enrichment factors, where enrichment factor is defined as the metal/Al ratio in atmospheric particulates divided by the metal/Al ratio in soils. For many of the trace metals, enrichment factors are of the same order of magnitude at high latitudes in both the Northern and Southern Hemispheres, and are larger at high latitude than at mid latitude.A simple mathematical model is used to calculate present-day enrichment factors in both hemispheres based on natural and anthropogenic influxes, effluxes, and transfer between hemispheres. The calculated enrichment factors are in good agreement with the observed enrichment factors for lithophile metals at both mid and high latitude, and for atmophile metals at mid latitude. However, calculated enrichment factors for atmophile metals are lower than observed enrichment factors at high latitude. To explain these results, we propose that for Hg, As and Se, and perhaps for other atmophile metals, there are significant fluxes from the sea surface to the atmosphere. If the estimated low-temperature fluxes of As, Se and Hg from the land and sea surfaces are included in the interference factor calculations for these metals, the factors are reduced to less than 100%.     

Organic compound tracers of fine soil and sand particles during summer in the metropolitan area of Riyadh,Saudi Arabia

Soil and sand fine particles, which may be resuspended as fine dust in the atmosphere, contain a variety of anthropogenic and natural organic components. Samples of fine soil and sand particles (sieved to <125 μM) were collected from the Riyadh area in the summer of 2003 and extracted with a mixture of dichloromethane and methanol (3:1, v:v). The derivatized total extracts were analyzed by gas chromatography–mass spectrometry in order to characterize the composition and sources of the organic components. Both anthropogenic and natural biogenic inputs were the major sources of the organic compounds in these extracts. Discarded plastics and vehicular emission products were the major anthropogenic sources in the fine particles from populated areas of the city. Their tracers were plasticizers, UCM, n-alkanes, hopanes and traces of steranes. Vegetation was the major natural source of organic compounds in samples from outside Riyadh and included n-alkanols, n-alkanoic acids, n-alkanes, methyl alkanoates, sterols and triterpenoids. Carbohydrates had high concentrations (42–54%) in all samples and indicate sources from decomposition of cellulose and/or the presence of viable microbiota such as bacteria and fungi. The results were also compared with the data obtained in winter 2002 and showed that anthropogenic inputs were higher in summer than in winter, whereas the opposite trend was observed for natural inputs.     

Microscopic morphology and elemental composition of size distributed atmospheric particulate matter in Urumqi, China

Microscopic morphology and elemental composition of atmospheric particulate matter (PM) in 13 different size fractions from 0.01 to 10 μm were studied using a Field Emission Scanning Electron Microscope with Energy-Dispersive Spectrometer (FESEM–EDX). The relative mass fractions exhibited a bimodal distribution with a major mode in the fine range (0.18–1 μm) and a minor mode in the coarse range (>1 μm), suggesting that the major pollution of PM is fine particles in this area of Urumqi atmosphere. The PM could be classified as follows: aluminosilicate/silica mineral, Si–Al rich fly ash, Fe oxide particle, Ti dominant particle, sulfate/carbonate crystal, carbonaceous aerosols (including soot, organic carbon, tar ball and irregularly shaped carbon). The soot and organic carbon with anthropogenic sources are dominant types in fine range samples (<1 μm). The natural source minerals and secondary synthesized sulfate/carbonate crystals were accumulated in the coarse range (>1 μm). Elemental composition of various types of particles (0.056–5.6 μm) was also analyzed by EDX. C, S, O, N, Si, Al, Fe, Ca, Na, K, Mg, Cl, F, Hg were detected in most samples. Si, Al and Ca accumulated in coarse fractions, while S and Hg mainly accumulated in fine fractions. Concentrations of 15 metallic elements in size range from 0.1 μm to 5.6 μm were divided into three groups based on their possible sources. (1) The crustal elements (Al, Mg, Fe, Mn and V), mainly present in coarse particles (>1 μm); and (2) the anthropogenic source elements (Ca, Ni, As, Cu, Pb, Cd and Hg). The concentrations of Ca and Ni increased with increasing particle size, while As, Cu, Pb, Cd and Hg showed opposite trends. As, Cu, Pb, Cd and Hg accumulated mainly in fine fraction (<1 μm). (3) The multi sources elements (Cr, Co and Se) possibly come from both natural and anthropogenic sources. High levels of heavy metals, especially Hg in nanosize particles, may pose great risk to human health.     

Geochemistry of trace metals and Pb isotopes of sediments from the lowermost Xiangjiang River, Hunan Province (P. R. China): implications on sources of trace metals

This paper reports a geochemical study of trace metals and Pb isotopes of sediments from the lowermost Xiangjiang River, Hunan province (P. R. China). Trace metals Ba, Bi, Sc, V, Cr, Mn, Co, Ni, Cu, Zn, Mo, Cd, Sn, Sb, Pb, Tl, Th, U, Zr, Hf, Nb and Ta were analyzed using ICP-MS, and Pb isotopes of the bulk sediments were measured by MC-ICP-MS. The results show that trace metals Cd, Bi, Sn, Sc, Cr, Mn, Co, Ni, Cu, Zn, Sb, Pb and Tl are enriched in the sediments. Among these metals, Cd, Bi and Sn are extremely highly enriched (EF values >40), metals Zn, Sn, Sb and Pb significantly highly (5 < EF < 20), and metals Sc, Cr, Mn, Co, Ni, Cu and Tl moderately highly (2 < EF < 5) enriched in the river sediments. All these metals, however, are moderately enriched in the lake sediments. Geochemical results of trace metals Th, Sc, Co, Cr, Zr, Hf and La, and Pb isotopes suggest that metals in the river sediments are of multi-sources, including both natural and anthropogenic sources. Metals of the natural sources might be contributed mostly from weathering of the Indosinian granites (GR) and Palaeozoic sandstones (PL), and metals of anthropogenic sources were contributed from Pb–Zn ore deposits distributed in upper river areas. Metals in the lake sediments consist of the anthropogenic proportions, which were contributed from automobile exhausts and coal dusts. Thus, heavy-metal contamination for the river sediments is attributed to the exploitation and utilization (e.g., mining, smelting, and refining) of Pb–Zn ore mineral resources in the upper river areas, and this for the lake sediments was caused by automobile exhausts and coal combustion. Metals Bi, Cd, Pb, Sn and Sb have anthropogenic proportion of higher than 90%, with natural contribution less than 10%. Metals Mn and Zn consist of anthropogenic proportion of 60–85%, with natural proportion higher than 15%. Metals Sc, Cr, Co, Cu, Tl, Th, U and Ta have anthropogenic proportion of 30–70%, with natural contribution higher than 30%. Metals Ba, V and Mo might be contributed mostly from natural process.     

Seasonal variations of water quality in a highly populated drainage basin,SE Brazil: water chemistry assessment and geochemical modeling approaches

The São João Drainage Basin is a very important and strategic waterbody located in the Lagos Region, Rio de Janeiro State, one of the most popular tourist regions of Brazil. However, the fast economic and subsequent population growth in that region has created untreated wastes from several anthropogenic activities, which include the trace metals disposal into the surface waterbody. This study aims to relate the major ions and trace metals behavior during a 1-year sampling campaign and to provide information about the sources of chemical constituents and the factors that control their concentrations in the three main fluvial compartments of the drainage basin, including the Juturnaíba Reservoir which has a crucial role for water supply in the Lagos Region. The chemical data reveal that rainfall is the main factor responsible for the physicochemical parameters and the water dissolved constituent’s variations. The geological and anthropogenic factors which are the main sources of water constituents were assessed by the Inorganic Chemical Index. Those data corroborate the great influence of rainfall and reveal the importance of anthropogenic sources of chemical constituents in some parts of the Juturnaíba Reservoir. The geochemical modeling suggests that hydrolysis reactions are primarily responsible for the trace metals availability in the three fluvial compartments in both dry and wet seasons, followed by carbonate and sulfate complexation.     

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Metals in lacustrine sediment have both anthropogenic and natural sources. Because of intensified human activities, the anthropogenic input of metal elements has exceeded the natural variability. How to distinguish the anthropogenic sources in lake sediments is one of the tasks in environmental management. The authors present a case study, which combined the geochemical and statistical methods to distinguish the anthropogenic sources from the natural background. A 56 cm core (core DJ-5) was collected from Dongjiu Lake, Taihu Lake catchment, China. The concentration distributions of Al, Ba, Be, Ca, Cd, Co, Cr, Cu, Fe, K, Li, Mg, Mn, Na, Ni, Pb, Sr, Ti, V and Zn in core DJ-5 indicated that Dongjiu Lake had serious Cd pollution, and the concentrations of Cr, Cu, Pb, Mn and Zn had also exceeded the Chinese State Standards of Soil Environmental Quality in the upper layer of the core. Using Al as a reference element, the other metals were normalized and compared with their baselines to calculate the enrichment factors (EFs). The principal component analysis (PCA) of metal concentrations was performed using ViSta6.4. The results of EFs and PCA indicated that the concentration variations of Cd, Cu, Pb, Mn and Zn were mainly caused by the anthropogenic sources, and the concentration variations of Cr and Ni were influenced by both the anthropogenic and natural factors, while the other metals were mainly derived from the natural sources. Intensified human activities within the lake catchment area resulted in the increase of heavy metal inputs directly and the acceleration of erosion which caused other metal elements to deposit in the aquatic environment. The results of this work will be useful in probing changes forced by humans in the lake environment and in adjusting human activity in restoring the lake environment.

Source and distribution of metals in urban soil of Bombay,India, using multivariate statistical techniques

Simplification of a complex system of geochemical variables obtained from the soils of an industrialized area of Bombay is attempted by means of R-mode factor analysis. Prior to factor analysis, discriminant analysis was carried out taking rock and soil chemical data to establish the anthropogenic contribution of metals in soil. Trace elements (Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, and Zn) are expressed in terms of three rotated factors. The factors mostly indicate anthropogenic sources of metals such as atmospheric fallout, emission from different industrial chimneys, crushing operations in quarries, and sewage sludges. Major elements (Na, Mg, Al, Si, P, K, Ca, Ti, Mn, and Fe) are also expressed in terms of three rotated factors indicating natural processes such as chemical weathering, presence of clay minerals, and contribution from sewage sludges and municipal refuse. Summary statistics (mean, standard deviation, skewness, and kurtosis) for the particle size distribution were interpreted as moderate dominance of fine particles. Mineralogical studies revealed the presence of montmorillonite, kaolinite, and illite types of clay minerals. Thus the present study provides information about the metal content entering into the soil and their level, sources, and distribution in the area.     

Magnetic signature of heavy metals pollution of sediments: case study from the East Lake in Wuhan,China

Detailed magnetic measurements and geochemical analyses were performed on 114 sediment samples collected from the East Lake, Wuhan city, China, to establish a possible link between the enhanced concentration of anthropogenic magnetic particles and heavy metals with known sources. Relatively higher magnetic susceptibility values (mass-specific, χ, >150 × 10⁻⁸ m³ kg⁻¹) were observed for samples near the pollution sources: e.g. the Wuhan Iron and Steel Company (WISC), the Qingshan Thermal Power Plant (QTPP), the banks (driveways) of the lake and near the sightseeing route of yachts on the lake. Moreover, χ is positively correlated to the concentration of Pb (correlation coefficient r = 0.682), but negatively or weakly correlated with both Zn and Cu. In contrast, anhysteretic remanent magnetization (ARM) is significantly correlated with these major heavy metals (r = 0.645 for Zn–ARM, 0.699 for Pb–ARM and 0.841 for Cu–ARM, respectively), which indicate that ARM serves a better indicator for the pollution of heavy metals in this lake. Thermomagnetic analysis combined with magnetic hysteresis measurements revealed that magnetites in the pseudo-single-domain/multidomain grain-size regions are dominant. Scanning electron microscopy and energy dispersive X-ray examinations of the magnetic extracts showed that these Fe-rich particles have different morphologies: orange-peel structure, hollow structure with adhered smaller particles, Zr-rich melted-like irregular particles, pear-shaped spherules and spherules with slick surfaces. These features are typical for particles produced by anthropogenic activities. Because of the genetic relationship between the environmental setting of the East Lake and the nearby pollution sources, this study suggests that in situ magnetic surveys are sensitive to evaluate the environmental pollution on the lake bottom.     

Heavy metals in Oka river sediments (Urdaibai National Biosphere Reserve, northern Spain): lithogenic and anthropogenic effects

 The Oka River basin is located in the Urdaibai National Biosphere Reserve, North Spain. In order to obtain a preliminary view of its environmental conditions, nitric acid extractable Fe, Mn, Zn, Pb, Cu, Cr, Ni and Co, organic matter content (L.O.I.), geochemical fractionation of heavy metals and mineralogical composition were analysed in surficial sediments (fraction <63 μm) collected in October 1991. Relatively high concentrations of metals occurred in a sampling site upstream, due to a local natural enrichment controlled by weathering of volcanic rocks. Geochemical fractionation confirmed the lithogenic origin of metals, which were mainly associated to the detrital phase. The significant increase of heavy metals found in some samples collected in the municipal area of Gernika suggested a pollution effect, related to anthropogenic wastes. Large amounts of metallic slags have been found mixed with the sediments upstream from this locality. Nevertheless, in view of their composition, it is unlikely that these slags constitute a significant source of heavy metals in the studied area. In a second sampling in October 1997 an apparent decreasing trend in some heavy metal levels was noted, particularly for Pb and Cu. Nowadays, enrichment factors relative to background values confirm moderate anthropogenic influence on Zn, Pb, Cu, Cr and Ni concentrations. However, heavy metal levels in the Oka river sediments are much lower than those detected in other major rivers of the Basque Country (Nervión, Urumea, Deba). Received: 7 July 1997 · Accepted: 4 July 1998     

Potential ecological risk assessment,enrichment, geoaccumulation,and source identification of metals in the surface sediments of Choghakhor Wetland,Iran

This study reported the first comprehensive research on identification of metal concentrations (Fe, Mg, Mn, Pb, Cd, Cr) in order to provide baseline data for future studies, identify possible sources, determine degree of pollution, and identify potential ecological risks of metals in surface sediments from Iran’s Choghakhor Wetland. The order of metal concentration was as follows: Fe > Mg > Mn > Pb > Cd > Cr, with mean concentrations of 6140.35, 1647.32, 289.03, 1.10, and 0.45 µg/g of dry weight, respectively. These results reveal that Choghakhor Wetland is not heavily polluted compared to other regions. The results of enrichment factor (EF) and geoaccumulation index (I _geo) showed that Fe, Pb, Mg, Cr, and Mn presented low levels of contamination and probably originated from natural sources. On the other hand, the results of EF and I _geo indices suggested that Cd concentrations in sediments of Choghakhor Wetland originated from anthropogenic sources. Based on the results of three sets of sediment quality guidelines, only Cd concentration in sediments of Choghakhor Wetland is a threat for aquatic organisms of Choghakhor Wetland. The results of multivariate analysis such as principal component analysis and cluster analysis showed that Fe–Mn, Cr–Mg, and Pb groups originated from natural sources, while Cd concentrations in sediments of Choghakhor Wetland originated from both natural and anthropogenic sources (mainly chemical fertilizers). To our knowledge, this is the first study about metal concentrations in sediments of Choghakhor Wetland, and because of low levels of these metals, these concentrations can be considered background levels for future investigation.     

Geochemical Control of Heavy Metal Concentrations and Distribution Within Bahia Blanca Estuary (Argentina)

Chromium and lead concentrations and distribution have been fully studied within Bahía Blanca estuary inner area, which is strongly influenced by urban and industrial stress. Not only metals dissolved in estuarine water but also those included in sediments and suspended particulate matters (SPM) were measured. In all cases, internationally standardized protocols were applied to metal measurements, including analytical quality check test through analysis of certified reference materials. Total metal contents from surface sediments and SPM were compared with those from a historical database of the area, as well as with values representing the natural geochemical baseline within the system. Results showed that heavy metal pollution is mainly localized in the areas close to both industrial effluents discharge system and urban sewage outfall discharge. Data from sequential extractions indicate that metals from anthropogenic sources (i.e., Pb) are potentially more mobile than those inherited from geological parent material (i.e., Cr). The influences of other potential sources of metals (i.e., streams, runoff) were also considered. SPM was clearly identified as the main carrier of the studied heavy metals within the system, and its significance to metals input into sediments and/or biota was verified. Finally, the normalization of measured metal concentrations against background reference elements (i.e., Al or Fe) has allowed to identify that most of the measured Cr was lithogenic, while a significant percentage of Pb was from anthropogenic origin within Bahía Blanca estuary.     

黑龙江省松嫩平原南部大气颗粒物地球化学特征及来源解析

研究采集了黑龙江松嫩平原南部28个夏季大气颗粒物样品,分析了不同粒径(TSP、PM10、PM2-5)样品中常量和微量元素含量,对元素浓度含量特征、元素间相关性和空间分布特征进行了分析,并使用富集系数法和因子分析法进行元素来源解析。研究表明：在PM10-100中富集的元素多在地壳中含量很高,重金属元素在PM2-5中高度富集,不同粒径大气颗粒物中各元素质量浓度整体水平为：大庆>绥化>哈尔滨>齐齐哈尔。富集因子分析表明：Fe、K、Ti、Mn、Co的富集因子小于1或非常接近1,Ca、Mg、Ni、Cr的富集因子大于1但仍小于10,Na、Zn、Cu、Cd、Pb、Se的富集因子大于10,表现出较为明显的人为来源特征。参照颗粒物不同源主要标识元素,对各元素进行主因子分析结果表明：松嫩平原南部大气可吸入颗粒物的主要来源是土壤扬尘,此外还有燃煤、垃圾焚烧、汽车尾气、碱尘大气传输、燃油和工业来源。     

Heavy-metal loadings related to urban contamination in the Kooloonbung Creek catchment,Port Macquarie,New South Wales

Urbanisation and industrial development lead to contamination of estuaries and streams with dispersed loadings of heavy metals and metalloids. Contributions of these elements also occur from natural sources. This study provides baseline geochemical data on the respective natural and anthropogenic inputs of Cu, Pb, Zn, Cd, As, Sb, Cr, Ni, Mn and S to estuarine, fluvial and wetland sediments, and adjacent soils, in the Kooloonbung Creek catchment that drains the Port Macquarie urban area in north coastal New South Wales. There have been anthropogenic additions of Cu, Pb, Zn and As from dispersed urban sources at Port Macquarie, but they are restricted to the local catchment and do not impact on the adjacent Hastings River estuary. The most contaminated sediments display enrichment factors up to 20 × for Cu and Pb, 9 × for Zn and 5 × for As relative to local background values. However, only one value (for Pb) exceeds National Water Quality Management Strategy interim sediment quality guideline (high) values. On the other hand, sediments and local soils are commonly strongly enriched in Cr, Ni and Mn, reflecting adjacent ultramafic and mafic rock substrate and lateritic regolith. Concentrations of Cr and Ni are commonly well above interim sediment quality guideline (high) values for sediments, but are in mineralogical forms that are not readily bioavailable. Sediment and soil quality guideline values consequently need to recognise natural enrichments and the mineralogical siting of heavy metals. Although dissolved concentrations of heavy metals in stream waters are commonly low, there is evidence for mobility of Cu, Zn, Fe and Al. Parts of the Kooloonbung Creek wetland area lie on sulfidic estuarine sediments (potential acid sulfate soils). Experimental oxidation of uncontaminated and contaminated sulfidic sediments leads to substantial dissolution of heavy metals under acid conditions, with subsequent aquatic mobility. The results warn about disturbance and oxidation of potential acid sulfate soils that have been contaminated by urban and natural heavy-metal sources.     

Metal pollution in coarse sediments of Tuticorin coast,Southeast coast of India

Indian coastal waters are subjected to considerable pressure from sewage and industrial wastes, which are responsible for the contamination of the coastal sediments with consequent loss in biosphere. The present investigation attempts to study the significance of coarse material (Sand fraction) in the distribution of metals in polluted marine sediments. The study revealed that coarse Sand component contains a relatively significant proportion of the anthropogenic metals (Cd, Cu, Pb and Zn) and therefore it cannot be neglected in metal pollution studies of coastal sediments. Further, the distribution of anthropogenic metals in both Silt + Clay and Sand fraction follow the same suit indicating similar pollution sources. From the total sediment type (Silt + Clay and Sand fraction) all anthropogenic metals had a noticeable amount (>50%) in the acid extractable (and potentially bio-available) fraction. This article stresses the importance of coarse fraction in metal pollution studies in Indian coastal system.     

Spatial distribution, source identification and affecting factors of heavy metals contamination in urban–suburban soils of Lishui city, China

An investigation on spatial distribution, possible pollution sources, and affecting factors of heavy metals in the urban–suburban soils of Lishui city (China) was conducted using geographic information system (GIS) technique and multivariate statistics. The results indicated that the topsoils in urban and suburban areas were enriched with metals, such as Cd, Cu, Pb, and Zn. Spatial distribution maps of heavy metal contents, based on geostatistical analysis and GIS mapping, indicated that Cd, Cr, Cu, Mn, Ni, Pb, and Zn had similar patterns of spatial distribution. Their hot-spot areas were mainly concentrated in the densely populated old urban area of the city. Multivariate statistical analysis (correlation analysis, principal component analysis, and clustering analysis) showed distinctly different associations among the studied metals, suggesting that Cr, Cu, Ni, Pb, Cd, and Zn had anthropogenic sources, whereas Co and V were associated with parent materials and therefore had natural sources. The Cd, Cr, Ni, Pb, and Zn contents were positively correlated with soil organic matter, pH, and sand content (p < 0.01). It is concluded that GIS and multivariate statistical methods can be used to identify hot-spot areas and potential sources of heavy metals, and assess soil environment quality in urban–suburban areas.     

Impact of land use types on the concentrations of metals in soils of urban environment in Nigeria

The concentrations of metals (Cd, Pb, Ni, Cr, Cu, Fe, Mn and Zn) were determined in soils under different land use types in an urban environment in order to study the impact of land uses on the concentrations of metals in the soils. The mean concentration range of metals for all land use types were 42.1 to 410, 11.2 to 118.2, 4388.2 to 31891.1, 9.7 to 65.4, 0.1 to 1.8, 4.7 to 35.2, 2.0 to 16.8 and 77.9 to 881.7 mg/kg, for Mn, Pb, Fe, Cu, Cd, Cr, Ni and Zn, respectively. The computed multiple pollution index (MPI) indicated that 67 % of the examined sites had MPI values between 1 and 20 i.e. at the pollution range, while 33 % of sites had MPI values of zero which indicated that these sites were not polluted with the studied metals. Zinc had the highest impact on the multiple pollution index values. Three main principal components were identified from the principal component analysis which include (i) Cu, Zn, Pb, Cr and Ni originating from both industrial and agricultural sources, and as well as automobile exhausts; (ii) Fe and Mn which originated from both natural and anthropogenic sources; (iii) Cd which its anthropogenic origin is different from components I and II. This study provided information on the sources of metals in the urban environment and extent of contamination associated with each land use, which are useful in the ranking of contaminated sites, environmental quality management, environmental forensic studies and guidance for remediation/redevelopment of contaminated land.     

Heavy metals in bottom sediments of great slave lake (Canada): A reconnaissance

Near the shores of Great Slave Lake, natural sources of heavy metals include gold and base metal deposits, mineralized greenstone belts and sedimentary bedrock, and uraniferous granites. Potential anthropogenic sources of heavy metals (As, Zn, Pb) include large gold and base metal extraction -processing facilities on the shores of the lake. Six sediment cores were collected on a traverse of the lake. Heavy metal concentrations and distributions are related to the regional bedrock geochemistry in the drainage basin. Higher uranium concentrations in the northernmost core are attributed to extensive uraniferous areas north of the lake. More subtle variations of concentration are related to sedimentologic characteristics and processes in the lake. The west basin is a natural sink for most of the heavy metals determined. Two centrally located west basin cores had mean zinc concentrations of 145 ppm, whereas cores closer to the north and south shores had mean concentrations of 80–110 ppm. Mn, Ni, and Pb were enriched in some of the cores from the area of shallower water near the MacKenzie River outlet, rather than in the central west basin. The enrichment is related to Mn-, Ni-, and Pb-rich amorphous coatings on quartz grains. Elevated zinc or lead levels from anthropogenic activities were not detected but elevated levels are suspected for arsenic. In the two cores from the center of the west basin, surface sediment contains up to 12 ppm arsenic, not high in comparison with noncontaminated freshwater lakes elsewhere in Canada but considerably elevated relative to concentrations of 1 ppm found deeper in the same cores. Contribution from the National Water Research Institute, Western and Northern Region. Presented at the 10th International Sedimentological Congress, Jerusalem, Israel, 1978.     

Isotopic evidence for the source of lead in the North Pacific abyssal water

The absence of accurate measurements of lead (Pb) isotopic composition in the North Pacific abyssal water has made it difficult to assess the relative importance of what are believed to be the two major Pb sources: the natural Pb introduced during preindustrial time and recent anthropogenic Pb resulting from leaded gasoline combustion and high temperature industrial activities. Here we report a vertical profile of seawater ²⁰⁶Pb/²⁰⁷Pb ratio and a meridional section of Pb concentration in the North Pacific Ocean. We observe 2-3-fold increases in Pb concentration along the deep-water flow path and a deep-water ²⁰⁶Pb/²⁰⁷Pb ratio (∼1.188) substantially lower than the pre-industrial value (∼1.210). These data suggest that anthropogenic Pb has invaded the North Pacific abyssal water and become the predominant Pb source there. A simple model calculation based on these data indicates that the anthropogenic Pb is transported to the deep ocean by sinking particles and that this Pb vertical flux has a ²⁰⁶Pb/²⁰⁷Pb ratio that decreased during the past two centuries.