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The Community Bureau of Reference (BCR) four-step sequential extraction has been adapted for fractionation of potentially toxic elements (PTE) in simulant airborne particulate matter (APM) samples presented on 47 mm filter dynamics measurement system (FDMS) filters as used in routine air quality monitoring. Simulants were prepared from an urban soil reference material and from BCR CRM 701, which is certified for analytes extractable by the BCR procedure. Analysis was performed by inductively coupled plasma mass spectrometry using an Agilent 7700x instrument. Fractionation patterns similar to the full-scale protocol were obtained when test portions as small as 0.0625 g were extracted in 2–3 mL of reagents. However, changing the extraction vessel used was found to affect the outcome. This highlights the operational nature of sequential extraction procedures and the need carefully to evaluate the effects of procedural modifications. When the method developed was applied to blank FDMS filters, large amounts of Zn were detected, especially in step 3, the oxidisable fraction, and step 4, the residual fraction. Despite this, following blank-correction, fractionation patterns similar to certified values were obtained for BCR CRM 701, with overall recoveries (∑(steps 1–4)) of 84.2-113%. Given the increased awareness of public health risks associated with poor air quality, a sequential extraction procedure specifically designed for use with APM samples collected during routine air quality represents a valuable tool for use in source apportionment and to improve understanding of human exposure to PTE through inhalation. [ABSTRACT FROM AUTHOR]

Several physiologically based extraction procedures have been proposed to estimate the fraction of the potentially toxic element content that would be bioaccessible in the human gastro-intestinal tract following accidental ingestion of soil. Many of these procedures are complex, they have been applied to a very limited range of soils, and most work has focussed on arsenic and lead. In the present study, a simplified, two-stage extraction, simulating the human stomach and intestine, was developed and applied to urban soil samples from ten public-access areas in the City of Torino, Italy. The human oral bioaccessibility of chromium, copper, nickel, lead and zinc was estimated. Lead and zinc bioaccessibilities were found to be higher in the stomach, but chromium was more bioaccessible in the intestine. Analyte concentrations were higher in roadside soils than in soils from parks. A higher proportion of the soil metal content was found in bioaccessible forms at roadsides than in parks. Comparison of the current findings with results of earlier work involving sequential extraction of the same soils indicated that the sequential procedure gave a relative, but not an absolute, indication of bioaccessibility. Calculations based on the bioaccessible analyte concentrations suggest that ingestion of only 2-3 g of some of the roadside soil samples from Torino could deliver the tolerable daily oral intake of chromium, nickel and lead to a 20-kg child. The developed procedure is useful for preliminary screening of soils and prediction of whether their bioaccessible metal contents are likely to pose a risk to human health. [ABSTRACT FROM AUTHOR]

As part of a harmonised assessment of urban soils (), we investigated the variability of metal content in soils from Aveiro (Portugal) and Glasgow (UK). Samples were collected from parks and other public open spaces in each city. Metal content (Al, Ca, Cr, Cu, Fe, Mn, Ni, Pb and Zn) and basic soil parameters (texture, CEC, pH, organic matter) were determined and data investigated using principal component analysis (PCA). The two cities differ in absolute levels of metal content reflecting industrial and historical development. Factors identified by PCA included anthropogenic (Cu, Pb, Zn), soil properties and geology, which explain variability when data were assessed based on metal content, soil properties and land use. This study highlights the contribution from geological background even in strongly urbanised environments. [ABSTRACT FROM AUTHOR]

This study evaluated the uptake of bioavailable metal (Cd, Cr, Cu, Fe, Pb and Zn) by woodlice (Isopoda) collected from public open spaces in urban areas of Renfrewshire, Central West Scotland, UK. The species Oniscus asellus and Porcellio scaber were collected at 13 different locations together with associated surface soil samples. Soils were subject to sequential extraction to evaluate metal availability and analyzed by ICP-AES and flame AAS for Cd, Cr, Cu, Fe, Pb and Zn concentrations. The soil samples had metal concentrations typical of general urban environments and the potentially toxic elements were well below published guideline values for contaminated sites. The metal concentration showed differing inputs of natural and anthropogenic sources. Metals were bioconcentrated in the order Cu>Cd>Pb>Cr>Zn>Fe for O. asellus and Cu>Zn>Cd>Cr>Fe for P. scaber. Principal Component Analysis of soil geochemical properties and Isopoda metal concentration identified metal to metal variation in uptake. Multiple linear regression analysis was applied in order to investigate the metal uptake in relation to soil properties (total metal concentration, pH and organic matter (OM)). The results showed that factors affecting metal concentration were both species and site specific. The most available forms of metals were generally poorly related to metal accumulation by woodlice, with the only exception being for Cu, which was related to the exchangeable soil fraction. Soil conditions e.g. pH and OM, influenced metal association within the soil and OM played a significant role in restricting uptake of Cr and Pb in particular. For most of the metals studied, despite differences in the environmental availability of the metals, accumulation from ambient soil concentration is controlled by ecological and physiological factors influencing metal assimilation, storage and excretion and that the two biological species vary considerably in their regulation of individual metals. [Copyright &y& Elsevier]

A study has been conducted to assess the quality and comparability of measurement of aqua-regia-soluble cadmium, chromium, copper, iron, manganese, nickel, lead, and zinc in urban soils within a small cohort of European research laboratories specializing in soil science or environmental analytical chemistry. An initial survey indicated that highly variable levels of analytical quality control (e.g. use of certified reference materials) were routinely implemented in participant laboratories. When a set of soil samples - differing in metal contents and in characteristics such as pH and organic-matter content - were exchanged and analysed, approximately 20% of results differed from target values by more than 25%. A principal-component analysis was applied to data for chromium, copper, nickel, lead, and zinc, and proved successful in assessing overall laboratory performance. The study indicates that greater prominence needs to be given to quality assurance and control if comparable data are to be generated in international, collaborative research projects. [ABSTRACT FROM AUTHOR]

The pollution level of potentially toxic elements (PTEs) in surface soils is detrimental to the ecosystem and human health. In this research, various indices such as an index of geo-accumulation (I geo), contamination factor (CF), degree of contamination (DC), and principal component analysis (PCA) were implemented to identify and evaluate the soil PTEs pollution; and then human health risk assessment model used to establish the link between heavy metals pollution and human health in the urban region of south India. Results exhibited that the mean concentration of Cr, Cu, Ni and Zn were found to be 1.45–6.03 times greater than the geochemical background values. Cr and Cu were the most profuse PTEs measured in the soils. The pollution indices suggest that soil of the study region is mainly moderate to highly polluted. The non-carcinogenic health risk assessment proposed by the United States Environmental Protection Agency (USEPA) suggested the mean hazard indices (HIs) were below one which denotes no significant of non-carcinogenic risks to both children and adults. Furthermore, carcinogenic risk assessment results advised ~80% of cancer risk was caused by Cr contents, while other heavy metals indicate that neither children nor adults in the study region were of carcinogenic risks. Image 1 • Potentially toxic elements (PTEs) contamination levels were estimated by using profound methods such as contamination factor, degree of contamination and index of geo-accumulation. • Assessment of non-carcinogenic and carcinogenic risks for children and adults were investigated in the study region. • Principal component analysis of PTEs were studied and also generated their spatial distribution maps in the investigated region. [ABSTRACT FROM AUTHOR]

This study focuses on the assessment of surface soils from industrially polluted region (El Tebbin) of southern Cairo, Egypt. The impact of agricultural, residential and industrial land use on soils developed from Nile river sediments has significantly compromised their function. Previous evidence has shown that the food chain is contaminated and enhances risk of contaminant exposure of the residential communities. This study investigates factors controlling potentially toxic element (PTE) distribution (Co, Ni, Pb, Cd, Zn, Cr and Cu) in El Tebbin soils and provide estimates of their mobility and bioavailability. The PTE concentrations are characterised by high variability as result of the variety of natural and anthropogenic influences. Highest spatial variability is found for Zn, Cd, Pb and Cu (C.V = 260.0%, 280.4%, 140.8% and 159.6% respectively) and enrichment factors indicate strong anthropogenic inputs. For Co and Ni, relatively low spatial variability (C.V = 65.8% and 45.0% respectively) with depletion in Ni suggests a relatively minor contribution from anthropogenic sources. For Cr, a more uniform distribution pattern showing depletion to minimal enrichment across the study area (C.V = 19.2%) reflects almost exclusive lithogenic control. Using principle component analysis (PCA) to explore concentration data reveals that the major inputs affecting PTE distribution are modified by primary soil properties (texture and pH). Their relative bioavailability (identified through sequential chemical extraction) relates strongly to local input sources. Those elements dominated by lithogenic input (Ni and Co) were found predominantly in soil residual fractions (95.6% and 90.5% respectively), while elements with stronger anthropogenic contributions (Cd, Zn, Pb and Cu) showed much higher portion in the more mobile and bioavailable fractions obtained from sequential chemical extraction, with average proportions of the totals being 62.6%, 57%, 40.7% and 39.2% respectively. Those PTEs with strong anthropogenic influence are potentially much more mobile for bioaccumulation in food chain with increased health risk for exposed residents and are confirmed by elevated concentrations of Cd, Zn, Pb and Cu recorded in local plant species. The main pollution sources were further highlighted by cluster analysis and showed vehicle traffic and specific industrial activities but which varied significantly from site to site. The identification of sources through the approach developed here allows prioritisation of monitoring and regulatory decisions by the local government to reduce further environmental exposure of the local population. [ABSTRACT FROM AUTHOR]

Abstract: The revised (four-step) BCR sequential extraction procedure has been applied to fractionate the chromium, copper, iron, manganese, nickel, lead and zinc contents in urban soil samples from public-access areas in five European cities. A preliminary inter-laboratory comparison was conducted and showed that data obtained by different laboratories participating in the study were sufficiently harmonious for comparisons to be made between cities and land types (e.g. parks, roadside, riverbanks, etc.). Analyte recoveries by sequential extraction, with respect to direct aqua regia digestion, were generally acceptable (100±15%). Iron, nickel and, at most sites, chromium were found mainly in association with the residual phase of the soil matrix. Copper was present in the reducible, oxidisable and residual fractions, whilst zinc was found in all four sequential extracts. Manganese was strongly associated with reducible material as, in some cities, was lead. This is of concern because high lead concentrations were present in some soils (>500mgkg−1) and the potential exists for remobilisation under reducing conditions. As would be expected, extractable metal contents were generally highest in older, more heavily industrialised cities. Copper, lead and zinc showed marked (and often correlated) variations in concentrations between sites within the same city whereas manganese and, especially, iron, did not. No overall relationships were, however, found between analyte concentrations and land use, nor between analyte partitioning and land use. [Copyright &y& Elsevier]