A survey of lead pollution in Chhattisgarh State, central India

Lead (Pb) is of major environmental concern due to its toxicological importance. The anthropogenic emission of Pb is at least 100 times higher than natural emissions. Soil and dust are significant sources of Pb exposure. Lead is generally immobile in soil and accumulates in the upper layers. Lead particles may enter homes via shoes, clothes, pets, and windows. Central India is rich in deposits of natural resource materials such as coal, pyrite, dolomite, and alumina that contain Pb and other heavy metals at the trace levels, and the substantial exploitation of these materials has tended to increased contamination of water and geological formations. Here we present data on Pb concentrations in the water, soil and sediment samples (n=158) collected from 70 locations in Chhattisgarh state, Raipur region. Lead concentrations in the surface water (n=44), groundwater (n=44), soils (n=60) and sediments (n=10) ranged from 6 to 1410, 3 to 52, 12.8 to 545, and 31 to 423 μg g⁻¹, with mean values of 305, 16, 102 and 190 μg g⁻¹, respectively. Most of the Pb fractions of >80% can be leached out with the chemical extractants EDTA, acetic acid, and hydroxylamine hydrochloride. Lead has accumulated in the soil clay fraction due to its relatively large surface area and decreases with increasing depth in the soil profile.     

Mercury contamination in agricultural soils from abandoned metal mines classified by geology and mineralization

Lead (Pb) contents and partition in soils collected from eleven vegetable-growing lands in Fujian Province, China, were investigated using a modification of the BCR (Community Bureau of Reference) sequential extraction procedure coupled with the Pb isotope ratio technique. Pb contents in Chinese white cabbage (B. Chinensis L.) grown on the lands for this study were also measured. Results showed that Pb concentrations in fifty samples of topsoil ranged from 456 to 21.5 mg kg⁻¹, with each mean concentration of six sampling lands exceeding the national standard (50 mg kg⁻¹); while Pb concentrations in edible portions of thirty-two vegetable samples ranged from 0.009 to 2.20 mg kg⁻¹, with four sampling sites exceeding the national sanitary standard (0.2 mg kg⁻¹). A significant correlation (r = 0.971, P < 0.01) of Pb contents in the acid-extractable fractions by BCR approach and the vegetables was observed, which indicates that the acid-extractable Pb is useful for evaluating the metal bioavailability for plants and potential risk for human health in soils. The determination of lead isotope ratios in different chemical forms of soils by BCR sequential extraction procedures provides useful information on the Pb isotopic composition associated with different soil fractions (especially in the acid-extractable fractions), and the result is helpful for the further study on controlling and reducing Pb contamination in vegetable-growing soils.     

Arsenic contamination in water,soil, sediment and rice of central India

Arsenic contamination in the environment (i.e. surface, well and tube-well water, soil, sediment and rice samples) of central India (i.e. Ambagarh Chauki, Chhattisgarh) is reported. The concentration of the total arsenic in the samples i.e. water (n=64), soil (n=30), sediment (n=27) and rice grain (n=10) were ranged from 15 to 825 μg L⁻¹, 9 to 390 mg kg⁻¹, 19 to 489 mg kg⁻¹ and 0.018 to 0.446 mg kg⁻¹, respectively. In all type of waters, the arsenic levels exceeded the permissible limit, 10 μg L⁻¹. The most toxic and mobile inorganic species i.e. As(III) and As(V) are predominantly present in water of this region. The soils have relatively higher contents of arsenic and other elements i.e. Mg, Al, Si, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Ga, Zr, Sn, Sb, Pb and U. The mean arsenic contents in soil of this region are much higher than in arsenic soil of West Bengal and Bangladesh. The lowest level of arsenic in the soil of this region is 3.7 mg kg⁻¹ with median value of 9.5 mg kg⁻¹. The arsenic contents in the sediments are at least 2-folds higher than in the soil. The sources of arsenic contamination in the soil of this region are expected from the rock weathering as well as the atmospheric deposition. The environmental samples i.e. water, soil dust, food, etc. are expected the major exposure for the arsenic contamination. The most of people living in this region are suffering with arsenic borne diseases (i.e. melanosis, keratosis, skin cancer, etc.).     

Lead speciation in indoor dust: a case study to assess old paint contribution in a Canadian urban house

Residents in older homes may experience increased lead (Pb) exposures due to release of lead from interior paints manufactured in past decades, especially pre-1960s. The objective of the study was to determine the speciation of Pb in settled dust from an urban home built during WWII. X-ray absorption near-edge structure (XANES) and micro-X-ray diffraction (XRD) analyses were performed on samples of paint (380–2,920 mg Pb kg⁻¹) and dust (200–1,000 mg Pb kg⁻¹) collected prior to renovation. All dust samples exhibited a Pb XANES signature similar to that of Pb found in paint. Bulk XANES and micro-XRD identified Pb species commonly found as white paint pigments (Pb oxide, Pb sulfate, and Pb carbonate) as well as rutile, a titanium-based pigment, in the <150 μm house dust samples. In the dust fraction <36 μm, half of the Pb was associated with the Fe-oxyhydroxides, suggesting additional contribution of outdoor sources to Pb in the finer dust. These results confirm that old paints still contribute to Pb in the settled dust for this 65-year-old home. The Pb speciation also provided a clearer understanding of the Pb bioaccessibility: Pb carbonate > Pb oxide > Pb sulfate. This study underscores the importance of taking precautions to minimize exposures to Pb in house dust, especially in homes where old paint is exposed due to renovations or deterioration of painted surfaces.     

Distribution and phytoavailability of antimony at an antimony mining and smelting area,Hunan, China

An investigation of the distribution, fractionation and phytoavailability of antimony (Sb) and other heavy metals in soil sampled at various locations in the vicinity of a Sb mine revealed elevated levels of Sb, most certainly due to the mining activities. The concentration of Sb in the soil samples was 100.6–5045 mg kg⁻¹; in comparison, the maximum permissible concentration for Sb in soil in The Netherlands is 3.5 mg kg⁻¹, and the maximum permissible concentration of pollutant Sb in receiving soils recommended by the World Health Organization is 36 mg kg⁻¹. The soil sampled near the Sb mine areas had also contained high concentrations of As and Hg. Root and leaf samples from plants growing in the Sb mine area contained high concentrations of Sb, with the concentration of Sb in the leaves of radish positively correlating with Sb concentrations in soil. The distribution of Sb in the soil showed the following order: strongly bound to the crystalline matrix > adsorbed on Fe/Mn hydrous oxides, complexed to organic/sulfides, bound to carbonates > weakly bound and soluble. Solvents showed varying levels of effectiveness in extracting Sb (based on concentration) from the soil, with , in decreasing order. The concentration of easily phytoavailable Sb was high and varied from 2.5 to 13.2 mg kg⁻¹, the percentage of moderately phytoavailable Sb ranged from 1.62 to 8.26%, and the not phytoavailable fraction represented 88.2–97.9% of total Sb in soils.     

Bioaccessibility of arsenic in soils developed over Jurassic ironstones in eastern England

Jurassic ironstones outcropping over parts of eastern England give rise to soils with arsenic concentrations in excess of the UK soil guideline value of 20 mg kg⁻¹ for residential areas. Total arsenic concentrations were determined for 73 ironstone derived soils and bioaccessible arsenic determined using an in vitro physiologically based extraction test. The bioaccessible arsenic concentration for these soils was found to be well below the soil guideline value with a mean concentration of 4 mg kg⁻¹ and a range of 2–17 mg kg⁻¹. The bioaccessible fraction ranges from 1.2 to 33%. Data from a sequential extraction test based on the use of aqua regia as the main extractant is presented for a subset of 20 of the soils. Chemometric data reduction is used to demonstrate that the bioaccessible arsenic is mainly contained within calcium iron carbonate (sideritic) assemblages and only partially iron aluminosilicates, probably berthierine, and iron oxyhydroxide phases, probably goethite. It is suggested that the bulk of the non-bioaccessible arsenic is bound up with less reactive iron oxide phases.     

Accumulation and phytoavailability of benzo[a]pyrene in an acid sandy soil

Effects of benzo[a]pyrene (B[a]P) on ryegrass (Lolium perenne L.) growth, plant accumulation and dissipiation of B[a]P in a red sandy soil (Hapli-Udic Argosol) were studied in a pot experiment. The plants were grown for 61 days in soil spiked with B[a]P at 0, 12.5, 25 and 50 mg kg⁻¹. Control pots without plants were also set up. Soil extractable B[a]P, plant shoot and root biomass, and concentrations of B[a]P in plant shoots and roots were determined. Ryegrass biomass was increased by addition of B[a]P and root B[a]P concentrations were significantly correlated with B[a]P application rate, but no such correlation was found for shoot B[a]P concentrations. This indicates that B[a]P enhanced the growth of the ryegrass. The extractable B[a]P concentration in the planted soil was significantly lower than that in the unplanted control soil at the rate of 50 mg B[a]P kg⁻¹. This indicates that ryegrass may help to dissipate B[a]P in soil at concentrations over 50 mg kg⁻¹ soil although the mechanism for this is not understood.     

Enrichment and exposure assessment of As,Cr and Pb of the soils in the vicinity of Stawell,Victoria, Australia

Stawell Gold Mine in NW Victoria, Australia, mines ores that contain large concentrations of As and significant quantities of the metals Pb and Cr. The aim of this research was to understand the dispersion, enrichment and probable exposure of these potentially hazardous elements around the mine site. Fifty-five surface soil samples were collected near the mine (<15 km) and analysed by ICP-MS/OES following bioavailable and four-acid extractions. Soils near the mine show greater concentrations of As, Cr and Pb than those near a regionally determined background. This is attributed to the combination of a natural geochemical halo around mineralization and anthropogenic dispersion due to mining and urbanization. Total As concentrations were between 16 and 946 mg kg⁻¹ near the mine in a regional background of 1–16 mg kg⁻¹. Total Cr concentrations were between 18 and 740 mg kg⁻¹ near the mine in a regional background of 26–143 mg kg⁻¹. Total Pb concentrations were between 12 and 430 mg kg⁻¹ near the mine in a regional background of 9–23 mg kg⁻¹. Dispersion of contaminant elements from the present ore processing is <500 m. The most enriched soils occur close to the town and are unrelated to present mining practices. The bioavailable As, Cr and Pb, soil ingestion rates and Risk Reference Doses were used to estimate health risks. An average toddler (12 kg) would need to consume at least 1.5 g, and most likely 12 g, of soil per day to show some symptoms of As toxicity. The maximum measured bioavailable As would pose a risk at average ingestion rates of 200 mg per day. Individuals with soil-eating disorders would exceed the safe daily consumption limits for As, and potentially Cr and Pb. Small children are not typically exposed to soil everyday, very few have soil eating disorders, and, therefore, the health risk from the soils around the mine is minimal.     

Influence of fertilizer and sewage sludge compost on yield and heavy metal accumulation by lettuce grown in urban soils

Previous research has demonstrated that many urban soils are enriched in Pb, Cd and Zn. Culture of vegetable crops in these soils could allow transfer of potentially toxic metals to foods. Tanya lettuce (Lactuca sativa L.) was grown in pots of five urban garden soils and one control agricultural soil to assess the effect of urban-soil metal enrichment, and the effect of soil amendments, on heavy metal uptake by garden vegetables. The amendments included NPK fertilizer, limestone, Ca(H₂PO₄)₂, and two rates of limed sewage sludge compost. Soil Cd ranged from 0.08 to 9.6 mg kg^–1; soil Zn from 38 to 3490 mg kg^–1; and soil Pb from 12 to 5210 mg kg^–1. Lettuce yield on the urban garden soils was as great as or greater than that on the control soil. Lettuce Cd, Zn and Pb concentrations increased from 0.65, 23, and 2.2 mg kg^–1 dry matter in the control soil to as high as 3.53, 422 and 37.0 mg kg^–1 on the metal-rich urban garden soils. Adding limestone or limed sewage sludge compost raised soil pH and significantly reduced lettuce Cd and Zn, while phosphate fertilizer lowered soil pH and had little effect on Zn but increased Cd concentration in lettuce. Urban garden soils caused a significant increase in lettuce leaf Pb concentration, especially on the highest Pb soil. Adding NPK fertilizer, phosphate, or sludge compost to two high Pb soils lowered lettuce Pb concentration, but adding limestone generally did not. On normally fertilized soils, Pb uptake by lettuce was not exceptionally high until soil Pb substantially exceeded 500 mg kg^–1. Comparing garden vegetables and soil as potential sources of Pb risk to children, it is clear that the risk is greater through ingestion of soil or dust than through ingestion of garden vegetables grown on the soil. Urban dwellers should obtain soil metal analyses before selecting garden locations to reduce Pb risk to their children.     

Crop demand of manganese

The peri-urban soils of Huelva, one of the first industrial cities in Spain, are subject to severe pollution problems primarily due to past poor management of industrial wastes and effluents. In this study, soil cores were collected in seven sites potentially contaminated with toxic chemicals arising from multiple anthropogenic sources, in order to identify trace elements of concern and to assess human health risks associated with them. In most soil core samples, total concentrations of As (up to 4,390 mg kg⁻¹), Cd (up to 12.9 mg kg⁻¹), Cu (up to 3,162 mg kg⁻¹), Pb (up to 6,385 mg kg⁻¹), Sb (up to 589 mg kg⁻¹) and Zn (up to 4,874 mg kg⁻¹) were by more than one order of magnitude greater than the site-specific reference levels calculated on the basis of regional soil geochemical baselines. These chemicals are transferred from the hazardous wastes, mainly crude pyrite and roasted pyrite cinders, to the surrounding soils by acid drainage and atmospheric deposition of wind-blown dust. Locally, elevated concentrations of U (up to 96.3 mg kg⁻¹) were detected in soils affected by releases of radionuclides from phosphogypsum wastes. The results of the human health risk-based assessment for the hypothetical exposure of an industrial worker to the surface soils indicate that, in four of the seven sites monitored, cancer risk due to As (up to 4.4 × 10⁻⁵) is slightly above the target health risk limit adopted by the Spanish legislation (1 × 10⁻⁵). The cumulative non-carcinogenic hazard index ranged from 2.0 to 12.2 indicating that there is also a concern for chronic toxic effects from dermal contact with soil.     

Genotypic variation in element concentrations in brown rice from Yunnan landraces in China

The mineral elements present in brown rice play an important physiological role in global human health. We investigated genotypic variation of eight of these elements (P, K, Ca, Mg, Fe, Zn, Cu, and Mn) in 11 different grades of brown rice on the basis of the number and distance coefficients of 282 alleles for 20 simple sequence repeat (SSR) markers. Six-hundred and twenty-eight landraces from the same field in Yunnan Province, one of the largest centers of genetic diversity of rice (Oryza sativa L.) in the world, formed our core collection. The mean concentrations (mg kg⁻¹) of the eight elements in brown rice for these landraces were P (3,480) > K (2,540) > Mg (1,480) > Ca (157) > Zn (32.8) > Fe (32.0) > Cu (13.6) > Mn (13.2). Mean P concentrations in brown rice were 6.56 times total soil P, so the grains are important in tissue storage of P, but total soil K is 7.82 times mean K concentrations in brown rice. The concentrations of the eight elements in some grades of brown rice, on the basis of the number and distance coefficients of alleles for 20 SSR markers for the landraces, were significantly different (P < 0.05), and further understanding of the relationship between mineral elements and gene diversity is needed. There was large variation in element concentrations in brown rice, ranging from 2,160 to 5,500 mg P kg⁻¹, from 1,130 to 3,830 mg K kg⁻¹, from 61.8 to 488 mg Ca kg⁻¹, from 864 to 2,020 mg Mg kg⁻¹, from 0.40 to 147 mg Fe kg⁻¹, from 15.1 to 124 mg Zn kg⁻¹, from 0.10 to 59.1 mg Cu kg⁻¹, and from 6.7 to 26.6 mg Mn kg⁻¹. Therefore, germplasm evaluations for Ca, Fe, and Zn concentrations in rice grains have detected up to sevenfold genotypic differences, suggesting that selection for high levels of Ca, Fe, and Zn in breeding for mass production is a feasible approach. Increasing the concentrations of Ca, Fe, and Zn in rice grains will help alleviate chronic Ca, Zn, and Fe deficiencies in many areas of the world.     

Sorption and bioavailability of arsenic in selected Bangladesh soils

The bioavailability of arsenic (As) in the soil environment is largely governed by its adsorption–desorption reactions with soil constituents. We have investigated the sorption–desorption behaviour of As in four typical Bangladeshi soils subjected to irrigation with As-contaminated groundwater. The total As content of soils (160 samples) from the Laksham district ranged from <0.03 to approximately 43 mg kg⁻¹. Despite the low total soil As content, the concentration of As in the pore water of soils freshly irrigated with As-contaminated groundwater ranged from 0.01 to 0.1 mg l⁻¹. However, when these soils were allowed to dry, the concentration of As released in the pore water decreased to undetectable levels. Remoistening of soils to field moisture over a 10-day period resulted in a significant (up to 0.06 mg l⁻¹) release of As in the pore water of soils containing >10 mg As kg⁻¹ soil, indicating the potential availability of As. In soils containing <5 mg As kg⁻¹, As was not detected in the pore water. A comparison of Bangladeshi soils with strongly weathered long-term As-contaminated soils from Queensland, Australia showed a much greater release of As in water extracts from the Australian soils. However, this was attributed to the much higher loading of As in these Australian soils. The correlation of pore water As with other inorganic ions (P, S) showed a strongly significant (P < 0.001) relationship with P, although there was no significant relationship between As and other inorganic cations, such as Fe and Mn. Batch sorption studies showed an appreciable capacity for both As^V and As^III sorption, with As^V being retained in much greater concentrations than As^III.     

Effect of cadmium alone and in combination with butachlor on soil enzymes

The ecological toxicity of cadmium (Cd, 10 mg kg⁻¹ of dry weight soil) and butachlor (10, 50 and100 mg kg⁻¹ of dry weight soil) in both their single and combined effects on soil urease and phosphatase was studied after 1, 3, 7, 14, 21 and 28 days exposure under controlled conditions in paddy and phaeozem soils. The results showed that Cd reduced the activities of urease and phosphatase at early incubation time (1–7 days), while the reduction almost disappeared at the end of the incubation. The effect of Cd on phosphatase was more pronounced than that on urease. The activities of urease and phosphatase were reduced by butachlor, while urease activity was significantly (P < 0.05 or P < 0.01) improved when the concentrations of butachlor were 10 and 50 mg kg⁻¹ at the end of the incubation. When Cd (10 mg kg⁻¹) was combined with butachlor (50 and 100 mg kg⁻¹), the activities of urease and phosphatase became lower than without combination at early incubation time, which indicated that the toxicity of Cd significantly increased (P < 0.05 or P < 0.01). However, when Cd (10 mg kg⁻¹) was combined with butachlor (10 mg kg⁻¹), the activities of urease and phosphatase became higher than those without combination at the end of the incubation, which indicated that the toxicity of Cd decreased. It was indicated that the combined effects depended largely on the incubation time and the concentration ratio of Cd and butachlor. In addition, it was showed that the combined effects of butachlor and Cd appeared different in paddy from phaeozem, which may be related to the different properties of these soils.     

Trace element concentration in wheat grain: results from the Swedish long-term soil fertility experiments and national monitoring program

Concentrations of trace elements in wheat grain sampled between 1967 and 2003 from the Swedish long-term soil fertility experiments were analyzed using ICP-MS. The long-term effect of inorganic and organic fertilization on trace metal concentrations was investigated including the impact of atmospheric deposition and myccorhiza, whereas other factors such as soil conditions, crop cultivar, etc. are not discussed in this paper. Mean values derived from 10 experimental sites were reported. Significantly declining Pb and Cd concentrations in wheat grain could be explained by lower atmospheric deposition. Mean Se contents in all samples were 0.031 mg kg⁻¹ grain dry weight. No samples had sufficiently high Se concentrations for human (0.05 mg Se kg⁻¹) or animal demand (0.1 mg Se kg⁻¹). Concentrations of Co in wheat grain were extremely low, 0.002–0.005 mg Co kg⁻¹ grain dry weight, and far below the minimum levels required by animals, which applied to all fertilizer treatments. A doubling of Mo concentrations in grain since 1975 resulted in Cu/Mo ratios often below one, which may cause molybdenosis in ruminants. The increase in Mo concentrations in crops correlated with the decline in sulfur deposition. Concentrations of Cu and Fe declined in NPK-fertilized wheat as compared to unfertilized or manure-treated wheat. Very low concentrations of Se and Co and low concentrations of Fe and Cu require attention to counteract risks for deficiencies. The main characteristic of the study is that there are few significant changes over time between different fertilizer treatments, but throughout there are low concentrations of most trace elements in all treatments. In general, good agreement between concentrations in wheat from the long-term fertility experiments and the national monitoring program indicate that values are representative.     

Heavy metal pollution in soil and plants at bone char site

This study determined the heavy metal concentration in soil and plants at a bone char site in Umuahia, Nigeria. Soil and plant samples collected in a randomized complete block design (RCBD) were analyzed for zinc (Zn), lead (Pb), cadmium (Cd), nickel (Ni), and arsenic (As). The concentration of metals in soil and plants in the vicinity of the bone char site are as follows: Zn (172?mg?kg^?1) and Ni (0.62?mg?kg^?1) in soil were highest at site P₃, Pb (2.37?mg?kg^?1) and As (0.08?mg?kg^?1) at site P₁, and Cd (18.30?mg?kg^?1) at site P₂. In plants, the concentrations of Zn (41.17?mg?kg^?1) and Cd (3?mg?kg^?1) were highest in Albizia ferruginea, Ni in Dialium guineense (0.09?mg?kg^?1), while Pb was in D. guineense (0.08?mg?kg^?1) and Spathodea companulata (0.06?mg?kg^?1). The levels of Zn, Cd, Pb, Ni, and As in soil ranged from 11.2 to 172, 2.68 to 18.2, 0.026 to 2.37, 0.33 to 0.62, and 0.02 to 0.08?mg?kg^?1, respectively. In plants, the concentration of Zn, Cd, Pb, and Ni ranged from 2.01 to 41.17, 0.12 to 3, 0.02 to 0.08, and 0.03 to 0.09?mg?kg^?1, respectively. There were significant correlations between Zn and Cd, and Pb and As in soil. The high concentration of Cd in soil might affect soil productivity.     

Risk assessment of heavy metal contamination in shrimp farming in Mai Po Nature Reserve, Hong Kong

An ecological survey was carried out to determine the sediment concentrations of nutrients and heavy metals and bioaccumulation of heavy metals in fish and shrimp including tilapia (Oreochromis mossambicus×O. nilotica), grey mullet (Mugil cephalus), gei wai shrimp (Metapenaeus ensis) and caridean shrimp (Macrobrachium nipponensis) in the traditional tidal shrimp ponds (gei wais) of Mai Po Nature Reserve, Hong Kong. The sediments collected from the landward sites contained higher nutrient contents, as well as zinc (Zn), chromium (Cr), copper (Cu), nickel (Ni) and cadmium (Cd) than those collected from the seaward sites, but vice versa for lead (Pb) and mercury (Hg). However, the concentrations of all metals were exceptionally high in the two sites located outside the reserve, suggesting that waters from Deep Bay might be the possible source of metal contamination affecting the reserve. All metals studied seemed to accumulate in the viscera of fish. Body size was the determining factor for the accumulation of heavy metals in caridean shrimp and gei wai shrimp but not fish. Concentrations of the metals studied in tissues of grey mullet and gei wai shrimp were found to be safe for human consumption. Concentrations of Cr in tilapia whole body (0.68–1.10 mg kg⁻¹ wet weight) were close to or over the guideline value of 1 mg kg⁻¹ set by the Food Adulteration (Metallic Contamination) Regulations of Hong Kong. Tilapia flesh and small caridean shrimp collected from gei wais were contaminated by Cr and Pb but still fit for human consumption. Caution is required if large caridean shrimp is to be consumed in large amounts continuously because the concentration of Pb exceeded the maximum permitted concentration (6 mg kg⁻¹). The rather high Cr concentrations in tilapia whole body should not be overlooked as the fish will serve as a food source for migratory birds visiting the site.     

Biomineralogy of human urinary calculi (kidney stones) from some geographic regions of Sri Lanka

Kidney stones (urinary calculi) have become a global scourge since it has been recognized as one of the most painful medical problems. Primary causative factors for the formation of these stones are not clearly understood, though they are suspected to have a direct relationship to the composition of urine, which is mainly governed by diet and drinking water. Sixty nine urinary calculi samples which were collected from stone removal surgeries were analyzed chemically for their Na, K, Ca, Mg, Cu, Zn, Pb, Fe and phosphate contents. Structural and mineralogical properties of stones were studied by XRD and FT-IR methods. The mean contents of trace elements were 1348 mg kg⁻¹ (Na); 294 mg kg⁻¹ (K); 32% (Ca); 1426 mg kg⁻¹ (Mg); 8.39 mg kg⁻¹ (Mn); 258 mg kg⁻¹ (Fe); 67 mg kg⁻¹ (Cu); 675 mg kg⁻¹ (Zn); 69 mg kg⁻¹ (Pb); and 1.93% (PO₄³⁻). The major crystalline constituent in the calculi of Sri Lanka is calcium oxalate monohydrate. Principal component analysis was used to identify the multi element relationships in kidney stones. Three components were extracted and the first component represents positively correlated Na-K-Mg-PO₄³⁻ whereas the␣second components represent the larger positively weighted Fe–Cu–Pb. Ca–Zn correlated positively in the third component in which Mn–Cu correlated negatively. This study indicates that during the crystallization of human urinary stones, Ca shows more affinity towards oxalates whereas other alkali and alkaline earths precipitate with phosphates.Contribution from the Environmental Geology Research Group (EGRG), Department of Geology, University of Peradeniya, Sri Lanka.     

Spatial distribution of PAHs in a contaminated valley in Southeast China

A survey was conducted on the accumulation and spatial distribution of PAHs in surface soils under different land use patterns in a valley in the Yangtze Delta region with an area of 10 km² containing 15 small copper- and zinc-smelting furnaces. Sixty-five topsoil (0–20 cm) samples were collected and 16 PAHs were determined. The average amount of all the 16 PAHs ranged from 0 to 530 μg kg⁻¹ (oven dry basis), with a mean concentration of 33.2 μg kg⁻¹. Benzo[a]pyrene and indeno[1, 2, 3, -cd]pyrene were the two main PAHs present at high concentrations, while pyrene and fluorene had very low concentrations. PAH concentrations were higher in uncultivated than in cultivated soils, and areas of woods and shrubbery had the␣lowest soil PAH contents. The average PAH-homologue concentrations ranked as follows: 5-rings >> 3-rings, 4-rings > 6-rings >2-rings. Much higher concentrations of PAHs were found in the southern part of the sampling area, perhaps due to deposition of airborne particles by the southeasterly winds in winter and spring. We conclude that the small smelting furnaces were the dominant source of PAHs that accumulated in the soils and the southeasterly winds led to the spatial distribution of PAHs in the topsoils. Land vegetation cover and soil utilization patterns also affected the accumulation and distribution of soil PAHs.     

Assessment of bioaccessibility and exposure risk of arsenic and lead in urban soils of Guangzhou City,China

Soil ingestion is an important human exposure pathway of heavy metals in urban environments with heavy metal contaminated soils. This study aims to assess potential health risks of heavy metals in soils sampled from an urban environment where high frequency of human exposure may be present. A bioaccessibility test is used, which is an in vitro gastrointestinal (IVG) test of soluble metals under simulated physiological conditions of the human digestion system. Soil samples for assessing the oral bioaccessibility of arsenic (As) and lead (Pb) were collected from a diverse range of different land uses, including urban parks, roadsides, industrial sites and residential areas in Guangzhou City, China. The soil samples contained a wide range of total As (10.2 to 61.0 mg kg⁻¹) and Pb (38.4 to 348 mg kg⁻¹) concentrations. The bioaccessibility of As and Pb in the soil samples were 11.3 and 39.1% in the stomach phase, and 1.9 and 6.9% in the intestinal phase, respectively. The As and Pb bioaccessibility in the small intestinal phase was significantly lower than those in the gastric phase. Arsenic bioaccessibility was closely influenced by soil pH and organic matter content (r ² = 0.451, p < 0.01) in the stomach phase, and by organic matter, silt and total As contents (r ² = 0.604, p < 0.001) in the intestinal phase. The general risk of As and Pb intake for children from incidental ingestion of soils is low, compared to their maximum doses, without causing negative human health effects. The exposure risk of Pb in the soils ranked in the order of: industrial area/urban parks > residential area/road side. Although the risk of heavy metal exposure from direct ingestion of urban soils is relatively low, the risk of inhalation of fine soil particulates in the air remains to be evaluated.     

Assessment of toxicity of heavy metal contaminated soils by the toxicity characteristic leaching procedure

The concentrations of Cu, Zn, Pb and Cd in soils near a lead–zinc mine located in Shangyu, Zhejiang Province, China, were determined and their toxicity was assessed using the toxicity characteristic leaching procedure (TCLP) developed by the United States Environmental Protection Agency. The TCLP method is a currently recognized international method for evaluation of heavy metal pollution in soils. The available levels of Cu, Zn, Pb and Cd were 8.2–36, 23–143, 6.4–1367 and 0.41–2.2 mg kg⁻¹, respectively, while the international standards were 15, 25, 5 and 0.5 mg kg⁻¹, respectively. Soils around the mine were more polluted with Zn and Pb, followed by Cd and Cu. Moreover, the levels of heavy metals in the soils extracted by TCLP indicated that extraction fluid 2 was more effective than extraction fluid 1 in extracting the heavy metals from the polluted soils and there was a positive correlation between fluids 1 and 2. Available heavy metal contents determined by TCLP were correlated with soil total heavy metal contents.