Approaches to soil remediation by complexometric extraction of metal contaminants with regeneration of reagents

Complexometric equilibrations were performed with six chelating reagents to mobilise Cu, Mn, Pb and Zn from a contaminated urban soil. The metal-laden aqueous extract was treated with sodium diethyldithiocarbamate (DEDTC) to precipitate the heavy metals from solution while liberating the chelating reagent. The aqueous supernatant fraction was then re-combined with the soil particulates to extract more pollutants. A sparing quantity of EDTA (ethylenediaminetetraacetic acid; 10 mmol) mobilised 32-54% of the 5 mmol of heavy metals from the soil with three cycles but only 0.1 and 1.0% of the iron and magnesium, respectively, was removed. Whereas DPTA (1,3-diamino-2-hydroxypropane-N,N,N',N'-tetraacetic acid) and citric acid also mobilised each of the heavy metals to some extent and continued to extract these metals during all three cycles, the DTPA (diethylenetriamine pentaacetic acid), although efficient initially, could not be recycled with these conditions. ADA [N-(2-acetamido)iminodiacetate] and SCMC [(S)-carboxymethyl-L-cysteine] were selective for copper and zinc but mobilised only Cu when recycled. An alternate means of regenerating the chelating reagent involved treatment of the aqueous extract with magnesium (Mg0) granules. Excess HEDC [bis(2-hydroxyethyl)dithiocarbamate] mobilised appreciable quantities (19-57%) of heavy metals from the soil and retained its complexing activity when recycled. An appreciable fraction of the mobilised Pb and Cu and a portion of the Zn were cemented to the surfaces of the excess magnesium whereas virtually all of the Fe and Mn was removed from solution as insoluble hydroxides.     

Heavy Metals Content in N. OleanderLeaves As Urban Pollution Assessment

Nerium oleanderL. (Oleander) leaves grown in Palermo city (Sicily, Italy) were collected from six sampling sites representing either areas of high traff{i}c and urbanisation density or areas far away from traffic (e.g. city gardens). Concentration of Al, Ba, Cr, Cu, Fe, Pb, Mg, Mn, and Zn were determined in leaf samples during two years. Multivariate analysis classified the sampling sites in four groups based on the metal content in vegetal leaves in agreement with traffic and human activity site. Many elements studied (Al, Ba, Fe, Mn Mg) arise from the soil composition and others such as Cr, Cu, Pb and Zn as pollutant of the soil. On the other hand, about 30% of Al, Fe Cr, Cu and Pb originate from aerial deposition on leaves. Although the results presented should be handled with caution N. oleandercan be considered as a means of assessing dust contamination in the urban environment.     

Assessment of background levels of trace metals in water and soil from a remote region of Himalaya

Selected trace metals were estimated by atomic absorption spectrometry in the water and soil samples collected from the remote region of Himalaya. The soil samples were analysed for soluble and acid extractable fraction of trace metals. In water samples, Ca, Na, Mg and K emerged as dominant contributors, whereas, Ca, Na, K, Mg, Fe and Pb were estimated at comparatively higher levels in the water extract of the soil. In case of acid extract of the soil samples, Ca, K, Fe, Mg, Mn and Na were found at elevated concentrations. Based on mean levels of the metals, following decreasing concentration order was observed in water samples: Ca > Na > Mg > K > Pb > Co > Cu > Zn > Mn > Cr > Fe > Cd > Li, however, in the acid extract of the soil, following order was noted: Ca > K > Fe > Mg > Mn > Na > Pb > Zn > Cr > Li > Cu > Co > Cd. The correlation study revealed appreciably diverse mutual relationships of trace metals in the water and soil samples. The multivariate cluster analyses exhibited divergent apportionment of trace metals in water and soil samples. Among the trace metals, Cd, Pb, Li, Zn, Cr, Cu, Mn and Co exhibited extreme to significant anthropogenic enrichment in the soil samples, while the rest of the metals were mostly contributed by the natural processes.     

Determination of total and EDTA extractable metal distributions in the colloidal fraction of contaminated soils using SdFFF-ICP-HRMS

Newly developed methods involving an on-line combination of sedimentation field-flow fractionation-inductively coupled plasma-high resolution mass spectrometry (SdFFF-ICP-HRMS) have been used to study the distributions of extractable heavy metals in a soil which had been treated with sewage sludge contaminated with Cu or Pb. The relationship of these metals with other elements in the colloidal fraction was also investigated. The colloidal fraction from the soil was obtained by repeated gravitational sedimentation and extracted with 0.11 M acetic acid, 0.1 M hydroxylamine hydrochloride, 0.05 M ethylenediaminetetraacetic acid disodium salt (EDTA) or aqua regia to assess the potential availability of the metals Cu and Pb. Large proportions of the Cu and Pb were extracted by EDTA, approaching that removed by aqua regia, whereas < 10% of the aqua regia extractable metals were removed by acetic acid and hydroxylamine chloride. The distributions of the heavy metals, the major mineral forming element (Al) and the elements forming sesquioxides (Fe and Mn) within different size classes (0.05-1 microm) of the colloidal fraction were measured using SdFFF-ICP-HRMS before and after extraction with EDTA. This information provides an insight into the composition of the colloids and the distributions of metal contaminants. In the contaminated soil colloids, the concentration of Fe, Mn and Pb is greatest in the smaller particles (<0.2 microm). In contrast, the Cu concentration is constant over the size range studied. Iron oxide surface coatings probably play a significant role in Pb adsorption on soil particles, but may be less important for Cu. The combination of selective chemical extraction, SdFFF and ICP-HRMS provides a means of determining the distribution of potentially available heavy metals within the colloidal fraction of contaminated soils.     

Metal Extraction from Road Sediment using Different Strength Reagents: Impact on Anthropogenic Contaminant Signals

Washoff of road deposited sediment into storm drainsystems is one of the major contributors to nonpoint sourcepollution in urban fluvial networks. These sediments contain avariety of potentially toxic organic and inorganic contaminants.Road sediment from 13 locations in an urban (non-industrialized)drainage basin, and soil from 10 background (control) locationswere collected to assess total and labile fractions of Al, Co,Cu, Fe, Mn, Ni, Pb and Zn. Four digestions, of varying strength,were used to assess contaminant levels, these included: a totalfour-acid digestion, a microwave-assisted digestion withconcentrated nitric acid (USEPA Method 3051), a 0.5 M `cold' HCl,and a 0.05 M EDTA (pH 7). Road sediment data indicate that Al,Co, Fe, Mn and Ni were primarily lithogenic in origin, while Cu,Pb and Zn showed very significant anthropogenic signals, mostprobably from vehicle-related sources. Median Pb concentrationenrichment ratios for the EDTA extraction were about 42,indicating an extreme anthropogenic signal. The weak extractants(HCl and EDTA) are considered in this study to be superior intheir ability to characterize the degree of anthropogeniccontamination and should be utilized more widely in environmentalcontaminant studies.     

Examination of honeys and flowers as soil element indicators

Detection of soil element deficiencies is time consuming, requiring a major commitment for field work and analysis. Bees concentrate some elements in their honey which could allow soil element concentrations to be predicted without having to take large numbers of soil samples. We measured 14 element concentrations in soil, sunflower, acacia flower and honey samples from two different regions of Hungary. Across sites, the elements with significant correlation coefficients between honey and soil concentrations, in descending order of probability, were Cu > Ba >Sr = Ni > Zn > Mn = Pb >As. Bioconcentration from soil to honey was similar for areas with acacia and sunflower flowers. In the macroelements, it was the greatest for K, S and P and least for Mg and Na, and in the microelements, greatest for B, then Zn, then Cu, then As, Mo and Sr and least for Fe, Ba, Mn and Pb. It is concluded that in acacia and sunflower-growing regions, honey can give an accurate estimate of soil element concentrations for Cu and Ba and provides relevant information for Sr, Ni, Zn, Mn, Pb and As.     

Major and trace element contents in apples from a cultivated area of central Greece

Forty-two soil and apple samples from central Greece were collected and analyzed with regards to the content in major (Ca, Fe, K, Mg, Na, P, and S) and trace elements (As, B, Ba, Cd, Co, Cr, Cu, Hg, Mn, Mo, Ni, Pb, Sb, Sc, Se, Sr, Ti, and Zn). Soil samples were analyzed by inductively coupled plasma atomic emission spectrometry, while for the apples inductively coupled plasma mass spectrometry was implemented. Several elements such as As, B, Cd, Cr, Cu, Fe, Mn, Ni, Pb, Se, Ti, and Zn, represent high concentrations in apples from the study area. These relatively high concentrations may be a consequence of the local geology, along with the excessive application of agricultural products such as fertilizers and agrochemicals.     

Assessment of trace elements in the shell layers and soft tissues of the pearl oyster Pinctada radiata using multivariate analyses: a potential proxy for temporal and spatial variations of trace elements

Concentrations of trace elements (Cd, Cu, Ni, Pb, V, and Zn) were determined in the soft tissues (adductor muscle and gills) of the pearl oyster Pinctada radiata and surficial sediments from two sampling sites located in the northern part of the Persian Gulf by Graphite Furnace Atomic Absorption Spectrophotometer (GFAAS). Moreover, the levels of Li, Mg, Al, Mn, Fe, Cu, Sr, Ba, Pb, and Zn were measured in two shell layers (prismatic and nacreous) using Laser Ablation Inductively Coupled Plasma Mass Spectrometer (LA-ICP-MS). There were significant differences between the sampling sites with regard to mean concentrations of Cu, Mn, and Al in the prismatic layers of the shells. But in terms of the soft tissues, only in the case of Ni accumulation in the muscle significant differences between the sites could be observed. No significant differences could be found between the sites from the elements concentrations in the sediments point of view. The levels of Cd, Cu, Ni, and Zn in the gills were markedly higher than those in the muscle. Concentrations of Mn, Mg, Li, and Cu in the prismatic layer were significantly higher than in the nacreous but the reverse case could be found for Sr. The patterns of metal occurrence in the selected tissues, shell layers, and sediments exhibited the following descending order: Zn, Ni?>?Cd, Cu?>?V, and Pb and Zn, Ni, Cd?>?Cu, V, and Pb for muscle and gills, respectively; Zn?>?Cu, Ni, Pb, Cd, and V for sediments; Mg?>?Sr, Mn, Li, Al, Fe, Ba, Cu, Pb, and Zn for the prismatic layer; and Sr, Mg?>?Mn, Al, Fe, Li, Ba, Cu, Pb, and Zn for the nacreous layer. In most cases, the temporal variations of the elements levels in the prismatic layer were clearer than those in the nacreous layer (especially for Li, Mg, Mn, Pb, and Fe). Comparison of the gained data from this study with the other relevant researches shows that in most cases the levels of the elements in this investigation either fell within the range for other world areas or were lower. Generally, it can be concluded that the shell (especially prismatic layer) of P. radiata can be considered as a suitable proxy for temporal and spatial variations of the trace elements (and probably some environmental parameters) in the study area.     

Assessment of metal pollution in urban road dusts from selected highways of the Greater Toronto Area in Canada

Over the last several decades, there has been increased attention on the heavy metal contamination associated with highways because of the associated health hazards and risks. Here, the results are reported of an analysis of the content of metals in roadside dust samples of selected major highways in the Greater Toronto Area of Ontario, Canada. The metals analysed are lead (Pb), zinc (Zn), cadmium (Cd), nickel (Ni), chromium (Cr), copper (Cu), manganese (Mn), calcium (Ca), potassium (K), magnesium (Mg) and iron (Fe). In the samples collected, the recorded mean concentrations (in parts per million) are as follows: Cd (0.51), Cu (162), Fe (40,052), Cr (197.9), K (9647.6), Mg (577.4), Ca (102,349), Zn (200.3), Mn (1202.2), Pb (182.8) and Ni (58.8). The mean concentrations for the analysed samples in the study area are almost all higher than the average natural background values for the corresponding metals. The geo-accumulation index of these metals in the roadside dust under study indicates that they are not contaminated with Cr, Mn and Ca; moderately contaminate with Cd and K; strongly contaminated with Fe and Mg; strongly to extremely contaminated with Ni and Pb; and extremely contaminated with Cu and Zn. The pollution load index (PLI) is used to relate pollution to highway conditions, and the results show that PLI values are slightly low at different samples collected from Highways 401 and 404 and high in many samples collected from Highway 400 and the Don Valley Parkway. Highway 400 exhibits the highest PLI values.     

Accumulation of some heavy metals in Hysterothylacium aduncum (Nematoda) and its host sea bream, Sparus aurata (Sparidae) from North-Eastern Mediterranean Sea (Iskenderun Bay)

The sea bream??s nematode and Sparus aurata, sampled from the Iskenderun Bay, Mediterranean, in March 2008 were analyzed by inductively coupled plasma?Catomic emission spectrometry for their some heavy metal (Cd, Cr, Cu, Fe, Hg, Mn, Mg, Pb, and Zn) levels. The metal concentrations of the parasites were compared to different organs (liver, muscle, gill, intestine, and skin) of the fish hosts. There were significant differences in Cd, Cr, Cu, Fe, Mn, Zn, Hg, Mg, and Pb concentrations in tissues of fish and its parasite. The parasite Cd, Cu, and Pb concentration was higher than the other tissues. Furthermore, significant differences were detected in the heavy metal accumulations between the parasitized and unparasitized fish tissues in Cd, Cu, Hg, and Pb concentrations. The Cd, Hg, and Pb concentrations were found in fish muscle at mean concentrations over the permissible limits proposed by the Food and Agriculture Organization.     

Baseline values for metals in soils on Fildes Peninsula, King George Island, Antarctica: the extent of anthropogenic pollution

Metal contents (Al, Ca, Cd, Cr, Cu, Fe, Hg, Mg, Mn, Ni, Pb, Ti, and Zn) have been measured in 30 surface soils on Fildes Peninsula, King George Island, Antarctica, yielding values (in milligrams kilogram(-1)) of 41.57-80.65 (Zn), 2.76-60.52 (Pb), 0.04-0.34 (Cd), 7.18-25.03 (Ni), 43,255-70,534 (Fe), 449-1,401 (Mn), 17.10-64.90 (Cr), 1,440-25,684 (Mg), 10,941-49,354 (Ca), 51.10-176.50 (Cu), 4,388-12,707 (Ti), 28,038-83,849 (Al), and for Hg (in nanograms gram(-1)) 0.01-0.06. Relative cumulative frequency analysis was used to determine the baseline values for the 13 metals. Compared with adjacent areas in Antarctica, Mg and Ni are significantly lower, but Cu is significantly higher than that of McMurdo Station. Enrichment factor analysis and the geo-accumulation index method were applied in order to determine the extent of anthropogenic contamination, and both show that Pb, Cd, and Hg have been significantly increased by human activities. Principal component analysis was used to identify the sources of metals in these soil samples.     

Season variations for metallic elements compositions study in plant Bidenens pilosa L. var. radiate Sch. in central Taiwan

The possibility of using Bidens pilosa L. var. radiate Sch leaves as environmental indicators of metallic element pollution has been investigated. Samples were analyzed with respect to the following pollutants: Zn, Mn, Cu, Ni, Pb, Cd, Cr, Fe, Ca, and Mg by using inductively coupled plasma atomic emission spectrometry. The results obtained on the metallic elements had the following average composition order: Ca > Mg > Fe, Mn > Zn > Cu > Ni > Pb > Cr > Cd for plant B. pilosa L. var. radiate Sch. at HK sampling site. In addition, the metallic elements had the following average composition order: Ca > Mg > Fe > Mn, Zn > Cu > Ni > Pb > Cr > Cd for plant B. pilosa L. var. radiate Sch. at TMP sampling site. Finally, the metallic elements had the following average composition order: Ca > Mg > Fe > Zn > Mn > Cu > Pb > Ni > Cr > Cd for plant B. pilosa L. var. radiate Sch. at LH sampling site. The seasonal average composition for metallic elements Mg, Fe, and Pb were ranked highest at HK sampling site in winter. In addition, seasonal average composition for metallic elements Mn, Zn, and Cd were ranked highest at TMP sampling site in winter. Finally, seasonal average composition for metallic elements Mg, Fe, and Cu were ranked highest at LH sampling site in spring.     

Concentrations of toxic heavy metals and trace elements in raw milk of Simmental and Holstein-Friesian cows from organic farm

Concentrations of toxic heavy metals (cadmium (Cd), lead (Pb)) and major nutritional and trace elements (Ca, Mg, P, Cu, Fe, Mn, Se, Zn) were analyzed in the milk of Simmental (n?=?20) and Holstein-Friesian (n?=?20) cows from an organic farm. Elements were determined using inductively coupled plasma emission atomic spectrometry. The conducted research showed that the milk of Simmental cows was characterized by the more advantageous mineral composition and lower concentration of noxious heavy metals compared to the milk of Holstein-Friesian cows. In the milk of Simmental cows, significantly lower concentrations of Pb and Cd (P?<?0.001) and Cu (P?<?0.05) and significantly higher concentrations of Fe and Mg (P?<?0.05) as well as nonsignificantly higher concentrations of Ca, Mn, and Se were found. In the milk of both breeds, very low Cu concentrations were recorded. The higher-than-recommended concentration of Pb in milk was also found. In the milk of both breeds, the significant positive correlations between concentrations of the following elements were observed: Pb–Cd, Pb–Se, Cd–Se, Cd–Mn, Zn–Cu, Zn–P, Ca–P, Ca–Mg, and Mg–P. The correlations between other elements within each of the analyzed breeds separately were also found.     

Use of tree bark for comparing environmental pollution in different sites from Buenos Aires and Montevideo

Multi-elemental profiles in bark of green ash trees collected in three representative areas of Buenos Aires, Argentina and Montevideo, Uruguay, were assessed as potential air pollution indicators. Ten elements: Al, Ba, Cr, Cu, Fe, Mg, Mn, Ni, Pb, and Zn, were measured using inductively coupled plasma optical emissions spectrometry from 70 samples collected in different environments: central, residential and rural (reference site), in order to compare spatial patterns of metal concentration. The samples used as a control were collected from a nature reserve situated far away from any significant influences, not even a nearby road. The reference site (RF) exhibited the lowest concentrations of Al, Cr, Fe, Ni, Pb, and Zn. However, Ba and Mn showed similar concentrations in all measured sites. Magnesium is the only element that had a greater concentration in RF than at the other sites. Copper did not show any clear pattern. The Centre of Montevideo (MVD) showed higher concentrations of Al, Ba, Cr, Fe, Pb and Zn than the Centre of Buenos Aires (BA). In the A sectors, Montevideo (SAMVD) showed higher concentrations of Al, Cu, Mg, Ni, and Zn and lower concentrations of Ba, Cr, Fe, Mn, and Pb than Buenos Aires (SABA). In the B sectors, Montevideo (SBMVD) showed higher concentrations of Al, Ba, Cu, Fe, Pb, and Zn and lower concentrations of Cr and Mg than Buenos Aires (SBBA), but similar concentrations of Mn and Ni. The use of bark for biomonitoring metals allowed us to detect concentration differences related to the urban fabric and the different kinds of vehicles and their fuels. In the cities, the differences in metal concentrations detected in bark were more striking between the sectors than between centers, despite CBA being much larger than CMVD in population, extension and vehicular traffic.     

抚顺市PM10中元素分布特征及来源分析

为了确定抚顺市PM10中元素的浓度特征及其来源,于2006—2007年的采暖季、风沙季和非采暖季在抚顺市的6个采样点采集PM10样品,并用等离子体原子发射光谱法(ICP-AES)测定样品中Ti、Al、Mn、Mg、Ca、Na、K、Cu、Zn、As、Pb、Cr、Ni、Co、Cd、Fe、V等17种元素的含量。结果表明,Al、Mg、Ca、Na、K、Mn、Fe等地壳元素在17种元素中占有较大比重,全年平均达到97.0%。富集因子分析结果表明,Cu、Zn、Pb、Cr、Co、Cd等元素在各季和各采样点明显受到人为活动影响,是典型的污染元素。主因子分析结果显示,土壤风沙尘、建筑尘、燃煤尘、道路扬尘、机动车尾气排放、金属冶炼、锰、铜、钛工业源是抚顺市PM10中元素的主要来源。     

Enhanced uptake of heavy metals in municipal solid waste compost by turfgrass following the application of EDTA

Enhancement of multiple heavy metal uptake from municipal solid waste (MSW) compost by Lolium perenne L. in a field experiment was investigated with application of EDTA. EDTA was added in solution at six rates (0–30 mmol kg^???1) after 50 days of plant growth. Two weeks later, plants were harvested for the first crop and then all the turfgrasses were mowed. After another 30 days of growth, EDTA was added again at above six rates to the corresponding sites and the second crop was harvested 2 weeks later. The results showed that EDTA significantly increased heavy metal accumulation in both crops of L. perenne. For the first crop, the concentrations of Mn, Ni, Cd, and Pb in the shoots increased remarkably with increasing EDTA supply, peaked at 25 mmol kg^???1 EDTA, and shoots of 0–5 cm height (shoots from medium surface to 5 cm height) had higher metal concentrations than 5–10 cm and >10 cm shoots. The highest concentration of Mn, Ni, Cd, and Pb was 2.3-, 2.3-, 2.6-, and 3.2-fold, respectively, in 0–5 cm shoots higher than control. For the second crop, the concentrations of Mn, Cu, and Pb in shoots were, in general, less than those in the first crop. However, the second crop was significantly higher (P?< 0.05) than the first crop in dry biomass, so the total amount of metals removed by the second crop was more than the first crop. In addition, EDTA significantly increased the translocation ratios of most heavy metals from roots to shoots. For the first crop, 38% of the total Zn, 51% of Cd, 49% of Pb, 60% Mn, 55% Ni, and 45% Cu taken up by the plant was translocated in the shoots of 0–5 cm height. Turfgrass would have potential for use in remediation of heavy metals in MSW compost or contaminated soils.     

The determination of the extractability of selected elements from agricultural soil

Concentrations of Ag, Al, Ba, Cd, Co, Cr, Cu, Fe, K, Mn, Na, Ni, Pb, Sr, and Zn—isolated by sequential extraction steps from apple orchard soil—were analyzed by inductively coupled plasma-atomic emission spectroscopy and compared to the total amount of metal in soil determined by XRF. The extractable amount of each metal was calculated by the extraction yields of the four steps. The LODs of the different elements in all extracts ware below 3 μg/L except for Ba (steps 1 and 2), Cu (step 1), Fe (all steps), K (steps 1–3), Mn (step 2), Na (steps 1–3), Ni (step 1), Pb (steps 1 and 4), and Zn (steps 1 and 2). The highest LOD (>10 μg/L) was found for Fe, K, and Na (step 1). The recovery of all metals after four sequential extraction steps was 90–112%. The repeatability (<1.1%), the intermediate precision (<5.3%), the day-to-day reproducibility (<6.2%), and the overall uncertainty of measurement (approximately 4–8.5%) for all analyzed metals supports the choice of the method used.     

Chemometric study on the trace metal accumulation in the sediments of the Cochin Estuary―Southwest coast of India

The distribution and accumulation of trace metals in the sediments of the Cochin estuary during the pre-monsoon, monsoon and post-monsoon periods were investigated. Sediment samples from 14 locations were collected and analysed for the metal contents (Mg, Cr, Mn, Fe, Co, Ni, Cu, Zn, Cd and Pb), organic carbon, total nitrogen, total sulphur and grain size. The data were processed using statistical tools like correlation, factor and cluster analysis. The study revealed an enrichment of Cd and Zn in the study area particularly at station 2, which is confirmed by enrichment factor, contamination factor and geoaccumulation index. The factor analysis revealed that the source of Cd and Zn may be same. The study indicated that the spatial variation for the metals like Mg, Cr, Fe, Co, Ni, Cu, Zn, Cd and Pb were predominant unlike Mn which shows a temporal variation. The strong association of trace metals with Fe and Mn hydroxides and oxides are prominent along the Cochin estuary. The anthropogenic inputs of industrial effluents mainly control the trace metals enrichment in the Cochin estuary.     

Assessment of heavy metal toxicants in the roadside soil along the N-5, National Highway, Pakistan

The assessment of the toxicants in roadside soil on regular basis has become extremely essential with the increase in awareness for the metal toxicity in the environment. The present study investigates the presence of toxic metals along National Highway (N-5), Pakistan. Averages of about 1.3 million per month of automobile vehicles ply on this route. Lead (Pb), zinc (Zn), copper (Cu), nickel (Ni), cadmium (Cd), cobalt (Co), manganese (Mn), mercury (Hg), and iron (Fe) were analyzed by atomic absorption spectrophotometry in roadside soil at the nine selected locations along the highway. Strong Pearson correlations (α = 0.05) were found between Pb and Zn (r(2)?= 0.887), Fe and Mn (r(2)?= 0.880), Hg and Cd (0.864), Cu and Zn (0.838), and Cu and Pb (0.814). The correlation between the elemental compositions of the main automobile components revealed vehicular traffic as the main non-point source of roadside soil pollution. Extremely high level of mercury, 144.05 mg kg(-1), was found at S5. It was revealed that the unregulated incineration and dumping sites of hazardous waste material along N-5 were also responsible for these contaminations. Multivariate analysis on the obtained data also disclosed the same interpretation. Cluster analysis of the data grouped Pb, Zn, and Cu at 85.23% similarity, whereas, Cd, Hg, and Ni were grouped at 78.75% similarity basis. The findings need swift action against the root cause of soil pollution.     

Heavy Metal Availability in Soil Amended with Composted Urban Solid Wastes

A study was performed to evaluate the pH and the availability of Zn, Cu, Mn, Pb, and Ni in soil amended with increasing doses of composted solid wastes, collected in Rio de Janeiro, Rio de Janeiro State and in Coimbra, Minas Gerais State, Brazil. The influence of the time elapsed between compost application to the soil and the sampling of the plant growth substrate (soil + compost) for pH and metal availability analyses was also examined. The availability of heavy metals in the soil, in the compost and in the substrate was evaluated using DTPA solution for metal extraction. The increase of the compost doses added to the soil resulted in the increase of the pH in the substrate. The addition of the compost from the bigger city, Rio de Janeiro, resulted in higher increase in soil pH and available Zn, Cu, Pb, and Ni levels as compared to the addition of the compost from the smaller city, Coimbra. Increasing the time elapsed between the compost application to the soil and the sampling of the mixture resulted in higher available Zn, Cu, Mn, and Pb levels. The addition of the compost from Rio de Janeiro resulted in substrate metal concentrations in the order Zn > Pb > Ni > Cu > Mn and for the Coimbra compost the metal concentrations in the substrate was Zn > Pb > Cu > Ni > Mn. The higher values of pH and available metals obtained for the bigger city were attributed to the greatest metal contamination of its compost.