Determination and speciation of heavy metals in sediments of the Juru River,Penang, Malaysia

The Juru River flows through largely urbanized areas and is grossly polluted by domestic wastes and discharges from pig farms. Other than carrying highly polluting organic materials, these wastes are also contaminated with heavy metals. To ascertain the extent of heavy metal pollution in the river, total and non-residual concentrations of Cu, Pb, Zn, Mn and Fe in sediment samples collected along the river were determined. The results indicate that both the total and non-residual metal concentrations in sediments can successfully be used to identify heavy metal pollution sources. The speciation of Zn, Mn and Fe in the sediment samples were investigated using a sequential leaching technique which identifies the elements among six operationally defined host fractions: (1) exchangeable, (2) carbonate and surface-associated, (3) easily reducible, (4) moderately reducible, (5) bound to organic matter and sulphides and (6) residual. The results indicate that Zn is mainly associated with the reducible fractions. Zn and Fe found in the moderately reducible fraction are significantly correlated, indicating that iron oxides is the preferred host phase by Zn.     

莱州湾表层沉积物中多氯联苯的测定方法及分布特征探究

以加速溶剂萃取法 (ASE)、索氏提取法/气相色谱法测定了莱州湾表层沉积物中的12种PCBs的浓度水平,探讨了它的分布特征并将两种方法进行了对比;同时测定了渤海湾北部海域表层沉积物中PCBs的含量,与莱州湾进行了比较。结果表明,莱州湾海域表层沉积物检测出8种多氯联苯(PCBs),浓度范围是N.D.~48.40 ng ·g ^-1dw。该海域多氯联苯的分布特征是近岸高,离岸低,由近岸向湾外延伸方向依次递减;渤海湾PCBs的浓度范围是0.15~68.30 ng ·g ^-1dw,和莱州湾差别不大。索氏提取法测定12种多氯联苯类化合物的基质加标回收率为78.00%~104.85%,相对标准偏差为0.95%~3.64%;加速溶剂萃取法的基质加标回收率为90.00%~102.00%,相对标准偏差为0.65%~2.75%;相对于渤海湾北部海域而言,莱州湾区域只是受到轻度污染,属于低风险生态区,不会对生物产生毒副作用;而前者则处于中度污染水平,可能会对生物产生毒副作用。     

Spatial distribution and risk assessment of heavy metals in sediments from a hypertrophic plateau lake Dianchi, China

The sediment in Dianchi Lake, a hypereutrophic plateau lake in southwest China, was investigated and the concentration of heavy metals (Cu, Cr, Ni, Zn, Pb, Fe, Mn, and Cd) in the sediment and sediment properties were determined. Their spatial distribution and sources were analyzed using multivariate statistics. The result indicated that the studied metals exhibited three distinct spatial patterns; that is, Cu, Pb, Zn, and Ni had a similar distribution, with a concentration gradient from the north to the south part of the lake; Cd and Cr presented a similar distribution; Fe and Mn presented a quite different distribution than other metals, which indicated their different sources and geochemistry processes. Correlation and cluster analysis (CA) provided origin information on these metals and the CA result was observed corresponding to those three spatial patterns. Principal component analysis further displayed metal source and driving factors; that is, Cu, Pb, Zn, Ni, Cd, and Cr were mainly derived from anthropogenic sources, and Fe and Mn were mainly the result of natural processes. Sediment assessment was conducted using geoaccumulation index (Igeo), potential ecological risk indices, and USEPA guidelines. The result indicated that, generally, Cd was the most serious risk metal; Pb and Cu posed moderate potential ecological risk; Cr, Zn, and Ni had slight ecological risk; Fe and Mn had little risk. Comparison of the assessment tools showed that each of the methods had its limitation and could bias the result, and the combined use of the methodologies and local knowledge on lithology or metal background value of soil in the practice would give a more comprehensive understanding of the metal risk or pollution. Statistical analysis also indicated that nutrients had different impacts on Fe, Mn, and trace elements, which implied that in the assessment of metal risk, nutrients impact should be taken into consideration especially for eutrophic waters.     

Application of DET (diffusive equilibrium in thin films) and DGT (diffusive gradients in thin films) techniques in the study of the mobility of sediment-bound metals in the outer section of Songkhla Lake, Southern Thailand

The techniques of diffusive equilibrium in thin films (DET) and diffusive gradients in thin films (DGT) were used in the outer section of Songkhla Lake, Thailand in order to obtain high-resolution profiles of total dissolved and labile trace metals in the sediment pore water and investigate benthic fluxes. Six DET probes and six DGT probes were deployed at the mouths of the Phawong, Samrong and U-Taphao canals. A close correspondence could be observed between the high-resolution profiles of Fe and As, revealing a close link between the reductive remobilization of Fe oxides and the reduction of As(V). Co and Ni DGT profiles showed a close correspondence with Mn, but a narrow mobilization zone. Reductive mobilization of Mn oxides and associated metals and sulfide precipitation control the behaviour of these metals. The DGT profiles of Cu, Zn, Cd and Pb show surface maximum, probably linked to organic matter degradation. Important benthic fluxes, especially for As, were found at the mouths of the U-Taphao and Phawong canals.     

Chemical forms and ecological risk of arsenic in the sediment of the Daliao River System in China

The chemical forms and ecological risk of As were characterized in the sediment of the Daliao River System (DRS), which has been affected by long-term intensive industrial, urban, and agricultural activities. Twenty-seven samples of surface sediment were collected and analyzed for total As content and that of its chemical forms. The results indicated that the average total As content in the sediment was 9.83 mg kg^− 1 but that the levels ranged from 1.57 to 83.09 mg kg^− 1. At the sites near cities, mining sites, and the estuary of the DRS, it is likely that adverse effects on aquatic organisms occur, due to As levels in the sediment that are often higher than the threshold effect level and occasionally higher than the probable effect level. A selectively sequential extraction indicated that the majority of As in the sediment was bound to Fe oxides (62.1%), with moderate proportions of residual As (19.8%), specifically adsorbed As (17.9%), and a low proportion of non-specifically adsorbed As (1.1%). In addition, the content of Fe in the sediment was positively and significantly correlated with the contents of amorphous and crystalline Fe oxide-bound As, confirming the crucial role of Fe oxides in immobilizing high amounts of As in superficial environments. The average molar ratio of As to Fe was 1.18 × 10^− 4 in the surface sediment of the DRS, similar to that of natural Fe oxides, but much lower than that of synthesized Schwertmannite. Therefore, the release of As under reduced and low pH conditions can cause serious problems for water resources and for living organisms.     

Speciation of Trace Metals in Coastal Sediments of El-Mex Bay South Mediterranean Sea–West of Alexandria (Egypt)

Sediments of El-Mex Bay estuary on the southern Mediterranean Sea have been analyzed for trace metals after sediment fractionation by sequential leaching. A sequential extraction procedure was applied to identify forms of Mn, Cu, Cd, Cr, Zn and Fe. The five steps of the sequential extraction procedure partitioned metals into: CH₃COONH₄ extractable (F1); NaOAC carbonate extractable (F2); NH₂OH.HCl/CH₃COOH reducible extractable (F3); H₂O₂–HNO₃ organic extractable (F4) and NHO₃/HClO₄/HF acid soluble residue (F5). Extracted concentrations of trace metals analyzed after all five steps, were found to be (μg/g) for Mn: 1930.2, Cu: 165.3, Cd: 60.9, Cr: 386.3, Zn: 2351.3 and Fe: 10895. Most of elements were found in reducible fraction except Fe found in acid soluble residue, characterizing stable compounds in sediments. Labile (non-residual) fractions of trace elements (sum of the first four fractions) were analyzed because they are more bioavailable than the residual amount. Correlation analysis was used to understand and visualize the associations between the labile fractions of trace metals and certain forms, since Fe-and Mn-oxides play an important role in trace metals sorption within aquatic systems, especially within El-Mex Bay sediments that characterized by varying metal bioavailability.     

Evaluation of metal contamination in sediments from north of Morocco: geochemical and statistical approaches

Concentrations of Fe, Mn, Cr, Cu, Ni, Pb, Zn, Cd and Hg were evaluated in surface sediments of two rivers from north of Morocco, known as Souani and Mghogha rivers. Significantly higher concentrations in mg kg^???1 dry weight (dw) of Mn (747.6 vs. 392.9), Cr (86.4 vs. 56.3), Zn (299.5 vs. 138.5) were found in sediment samples from Mghogha when compared with Souani river. Average concentrations of Cd and Hg in several sediment samples from both rivers were above the effect range median that predicts toxic effects to aquatic organisms. The calculation of enrichment factors showed that Mn, Cr, Cu and Ni were depleted, whereas Pb and Hg were enriched. The results of geoaccumulation index revealed that sediments of both rivers were unpolluted with most of the metals and moderately contaminated with Fe and Hg. Some of elevated concentrations of Hg, principally in Mghogha River, were due to anthropogenic sources including the direct discharges of industrial zone.     

Arsenic mobilization in the Brahmaputra plains of Assam: groundwater and sedimentary controls

Arsenic (As) mobilization to the groundwater of Brahmaputra floodplains was investigated in Titabor, Jorhat District, located in the North Eastern part of India. The groundwater and the aquifer geochemistry were characterized in the study area. The range of As concentration in the groundwater varies from 10 to 440 μg/l with mean concentration 210 μg/l. The groundwaters are characterized by high dissolved Fe, Mn, and HCO₃ ^? and low concentrations of NO₃ ^? and SO₄ ^2? indicating the reduced conditions prevailing in the groundwater. In order to understand the actual mobilization processes in the area, six core drilling surrounding the two target tube wells (T1 and T2) with high As concentration (three drill-cores surrounds each tube well closely) was done. The sediment was analyzed its chemical, mineralogical, and elemental compositions. A selective sequential extraction suggested that most of the As in the sediment is bound to Fe oxides fractions (32 to 50 %) and the competition for adsorption site by anions (PO₄ ^3?) also accounts to significant fractions of the total arsenic extracted. High variability in the extraction as well as properties of the sediment was observed due to the heterogeneity of the sediment samples with different chemical properties. The SEM and EDX results indicate the presence of Fe, Mn coating along with As for most of the sample, and the presence of As associated minerals were calculated using PHREEQC. The mobilization of As into the groundwater was anticipated to be largely controlled by the reductive dissolution of Fe oxides and partly by the competitive anions viz. PO₄ ^3?.     

Study of leachability and fractional alteration of arsenic and co-existing elements in stabilized contaminated sludge using a flow-through extraction system

This study investigates the stabilization of As in the contaminated sludge after treatment with MnO(2) or Ca(OH)(2), and the influence of the stabilizing materials on the leachability of the co-existing elements Pb and Zn. By exploiting a continuous-flow assembly facilitating a modified Wenzel's sequential extraction scheme (designed for the fractionation of arsenic), it is possible to ascertain the leachability, mobility and fractional alteration of these elements under stimulated natural (flow-through) leaching conditions. The fractionation data show that more than 80% of As, Pb and Zn in the untreated sludge are bound in the amorphous Fe oxides fraction and residual fraction. The addition of MnO(2) has only an insignificant effect on As fractional transformation, while Ca(OH)(2) caused an increase in As mobility. For Pb, the decrease in leachability was clearly visible. The extractable Pb was reduced by 18% and 40% in stabilized MnO(2) and Ca(OH)(2) sludge samples, respectively. Unlike that of Pb, the mobility of Zn was not affected by the additives used. Their fractional distribution patterns before and after the stabilization process remained the same. The ability to produce detailed leaching profiles for As and other elements (Pb, Zn, Ca, Mn and Fe) meant that elemental associations in individual fractions could be examined. From the MnO(2)-treated sludge, the coincidence of the As, Pb, Zn, Fe, and Mn peaks seems to indicate a close association of these elements in the Fe-oxides-bound fraction. Furthermore, the leaching profiles may be used as evidence of a strong affinity between these elements and added MnO(2).     

Fractionation of heavy metals and phosphorus in suspended sediments of the Yamuna river,India

The Yamuna river is the largest tributary of the Ganges river system. It originates in the Himalayas and flows through a varied geological terrain encompassing a large basin area. Metals Fe, Mn, Pb, Zn, Cu in different chemical fractions of suspended sediments such as exchangeable, carbonates, Fe–Mn oxides, organics and residual fractions were studied. Phosphorus associated with different chemical forms are discussed. The metals are mostly associated with residual fractions in the sediments followed by organics, Fe–Mn oxides, exhangeable and carbonates. Intensive use of chemical fertilizers and pesticides in agriculture in the basin affects the high inorganic phosphorus content in sediments.     

Distribution and Statistical Analysis of Leachable and Total Heavy Metals in the Sediments of the Suez Gulf

The concentrations of nine heavy metals (Cd, Co, Cr, Cu, Fe, Mn, Ni, Pd and Zn) in the labile and total fractions of muddy and sandy sediment samples collected from twelve sites in Suez Gulf during April 1999 were studied to evaluate the pollution status of the Suez Gulf. The enrichment factors (EF) for each element were calculated. There are extremely high concentrations of Cd, Ni, Pb and slightly concentration of Cr and Cu in both muddy and sandy sediments. The concentration of Zn was moderately high and can be considered as seriously contaminate Metal pollution index (MPI) shows high values ranged between 46 to 156 and 40 to 232 for both sandy and muddy sediments, respectively. Concentrations of heavy metals were normalized against iron for total fraction in both of sandy and muddy sediments. Principal component analysis (PCA) was studied on the data matrix obtained and represented three-factor model explaining 92.22% for labile and 88.82% for total fractions of muddy sediment. The main source of contamination is the offshore oil fields and industrial wastes. This is largely a result of ineffective and inefficient operation equipment, illegal discharge of dirty ballast water from tankers and lack of supervision and prosecution of offenders.     

Metal release from serpentine soils in Sri Lanka

Ultramafic rocks and their related soils (i.e., serpentine soils) are non-anthropogenic sources of metal contamination. Elevated concentrations of metals released from these soils into the surrounding areas and groundwater have ecological-, agricultural-, and human health-related consequences. Here we report the geochemistry of four different serpentine soil localities in Sri Lanka by coupling interpretations garnered from physicochemical properties and chemical extractions. Both Ni and Mn demonstrate appreciable release in water from the Ussangoda soils compared to the other three localities, with Ni and Mn metal release increasing with increasing ionic strengths at all sites. Sequential extraction experiments, utilized to identify “elemental pools,” indicate that Mn is mainly associated with oxides/(oxy)hydroxides, whereas Ni and Cr are bound in silicates and spinels. Nickel was the most bioavailable metal compared to Mn and Cr in all four soils, with the highest value observed in the Ussangoda soil at 168?±?6.40 mg kg^?1 via the 0.01-M CaCl₂ extraction. Although Mn is dominantly bound in oxides/(oxy)hydroxides, Mn is widely dispersed with concentrations reaching as high as 391 mg kg^?1 (Yudhaganawa) in the organic fraction and 49 mg kg^?1 (Ussangoda) in the exchangeable fraction. Despite Cr being primarily retained in the residual fraction, the second largest pool of Cr was in the organic matter fraction (693 mg kg^?1 in the Yudhaganawa soil). Overall, our results support that serpentine soils in Sri Lanka offer a highly labile source of metals to the critical zone.     

Biomonitoring study of heavy metals in biota and sediments in the South Eastern coast of Mediterranean sea, Egypt

Concentrations of Cd, Cu, Co, Zn, Mn and Fe were determined in biota and sediment samples collected from the Eastern Harbour and El-Mex Bay in the Mediterranean Sea, Egypt. The levels of Cu, Co, Zn, Mn and Fe in the macroalgae, Ulva lactuca, Enteromorpha compressa (green algae) and Jania rubens (red algae), recorded high concentrations except for Cd. Moreover, Fe was the most predominant metal in the seaweed. The two species of bivalves, Donax trunculus and Paphia textile, showed different amounts of metals in their tissue. The abundance of heavy metal concentrations in the mussel samples was found in the order Fe> Zn> Mn> Cu> Co> Cd and Fe> Zn> Mn> Cu> Cd> Co, respectively for the two species. The metals concentrations were generally higher compared with the previous studies in mussels from the same area. The levels of metals accumulated in the investigated fish samples, Saurida undosquamis, Siganus rivulatus, Lithognathus mormyrus and Sphyraena sphyraena, were higher than those of Marmara Sea (Turkey), for Co and Cd and lower for Cu, Zn, Mn and Fe. El-Mex Bay having the highest metals concentration in sediments as their order of abundance were Fe> Zn> Mn> Cu> Cd> Co. Nevertheless, a high variability in the metal levels occurs among the studied algae and biota and also between the investigated Harbour. A significant correlations (p < 0.05) were found for each of Zn and Fe in P. textile and of Co in D. trunculus relative to their concentrations in surficial sediments.     

Assessment of trace metal pollution in surface sediments of Nemrut Bay, Aegean Sea

Surface sediments collected from nine stations in Nemrut Bay, Aegean Sea were analyzed for trace metals (Hg, Cd, Pb, Cr, Cu, Zn, Mn, Ni, Fe, As, and Mg) and grain sizes. The results were compared with the numerical sediment guidelines used in North America as well as literature values reported for similar studies conducted in Izmit Bay and Izmir Bay. The metal levels were also evaluated according to the enrichment factor and contamination factor analyses. The analyses revealed significant anthropogenic pollution of Hg, Pb, Zn, and As in the surficial sediments of Nemrut Bay.     

Trace elements as tracers of environmental pollution in the canal sediments (alluvial formation of the Danube River, Serbia)

The purpose of this study was to examine the levels of trace elements and to discuss the origin and mobility of these contaminants in the canal sediments (alluvial formation of the Danube River). The most significant fractions binding all of the studied elements were oxides and silicates. The high proportion of elements in the residual fraction and the generally low contents of extractable elements reflected the background geochemical conditions. The contents of trace elements (except Hg and As) were dominantly controlled by the presence of Fe and Mn oxides as well as by the grain size and the geochemical composition of the sediment. The studied alluvial sediments were not heavily contaminated; there were only few sites where an anthropogenic influence on the concentrations of some metals (Cu, Cd, Zn, and Pb) was noticed. The results from this study show that impact of Pan?evo industrial zone on the quality of the Danube River and its contamination with trace element is minor.     

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.     

Chemical fractionation of heavy metals in urban soils of Guangzhou, China

Knowledge of the total concentration of heavy metals is not enough to fully assess the environmental impact of urban soils. For this reason, the determination of metal speciation is important to evaluate their environment and the mobilization capacity. Sequential extraction technique proposed by the former European Community Bureau of Reference (BCR) was used to speciate Cd, Cu, Fe, Mn, Ni, Pb, and Zn in urban soils from Guangzhou into four operationally defined fractions: HOAc extractable, reducible, oxidizable, and residual. The Cu, Fe, Ni, and Zn were predominately located in the residual fraction, Pb in the reducible fraction, and Cd and Mn within the HOAc extractable fraction. The order of Cd in each fraction was generally HOAc extractable > reducible > residual > oxidizable; Cu and Fe were residual > reducible > oxidizable > HOAc extractable; Mn was HOAc extractable > residual > reducible > oxidizable; Ni and Zn were residual > reducible > HOAc extractable > oxidizable; and Pb was reducible > residual > oxidizable > HOAc extractable. Cadmium was identified as being the most mobile of the elements, followed by Mn, Zn, Ni, Cu, Pb and Fe. Iron–Mn oxides can play an important role in binding Cd, Cu, Ni, Pb, and Zn and in decreasing their proportion associated with the residual fraction in the soils. With total concentrations of Cd, Cu, Ni, Pb, Zn, and Mn increase, these metals more easily release and may produce more negative effects on the urban environment.     

Sediment quality in the Douro river estuary based on trace metal contents, macrobenthic community and elutriate sediment toxicity test (ESTT)

The aim of this study was to evaluate the sediment quality in the mesotidal Douro River estuarine environment, in order to identify areas where sediment contamination could cause ecosystem degradation. Samples were obtained in five locations and sediment characterised for grain size, total organic matter, total-recoverable metals (Al, Fe, Cu, Pb, Cr, Ni, Cd, Zn and Mn), as well as acid volatile sulfide (AVS) and simultaneously extracted metals (SEM). In situ effects were evaluated by examining the macrobenthic community structure. An elutriate sediment toxicity test (ESTT) was used to estimate the amount of metals and nutrients that could be exchanged with the water column through resuspension, and its positive or negative effects on the growth of the micro-alga Emiliania huxleyi in a 10 day test. Anthropogenic metal contamination was identified at the north bank of the Douro estuary, with deleterious effects on the macrobenthic community, namely decrease in number of species and diversity. This contamination could possibly also be toxic for water column organisms, in case of resuspension, as shown by the ESTT. Sediments from the salt marsh at the south bank showed an impoverished macrobenthic community and elutriate toxicity, which appeared to be due to anaerobic conditions. This study clearly shows the usefulness of the ESST approach to assess the biological effect of resuspension of estuarine sediments.     

Attenuation of dissolved metals in neutral mine drainage in the Zambian Copperbelt

Behaviour of metals like Cu and Co was studied in nearly neutral (pH ?? 6.4) mine drainage seepage in a stream downgradient of a tailing dam at Chambishi site in the Copperbelt of Zambia. They are attenuated by precipitation of ferruginous ochres that incorporate significant quantities of metals. Using chemical analysis, X-ray powder diffraction and M?ssbauer spectroscopy, we show that the ochres are composed mostly of amorphous ferric hydroxide. Close to the seepage face, the total Fe content of ochres increases due to precipitation of amorphous ferric hydroxide, but total Fe in sediment decreases further downstream. The stream then flows through wetland (dambo) where the remaining fraction of metals is removed. During rainy periods, increased flow rate may result in re-suspension of ochres, increasing thus the mobility of metals. Major ions like sulphate are conservative at the start of the dry period (May), but gypsum may probably precipitate later at the end of the dry period. Sequential extractions of bulk sediments indicate that Mn behaves differently to Fe, with a trend of increasing Mn with distance from the tailing dam. There is much more Fe than Mn in residual (Aqua Regia) fraction, indicating that amorphous ferric hydroxides are transformed to more crystalline phases deeper in sediment. Environmental impact of mine drainage is relatively limited due to its neutral character.     

Fractionation of eleven elements by chemical bonding from airborne particulate matter collected in an industrial city in Argentina

A four-step chemical sequential extraction procedure was used to evaluate the distribution of Al, As, Cr, Cu, Fe, Mn, Ni, Pb, Ti, V and Zn in airborne particulate matter collected on glass fibre filters using a high-volume sampler. Two sets of samples were collected in 2001 (winter and summer campaigns) in representative zones of an industrial city of Argentina. The leaching scheme was applied to PM-10 particles and consisted in extracting the elements in four fractions, namely soluble and exchangeable elements; carbonates, oxides and reducible elements; bound to organic matter and sulfidic metals; and residual elements. Metals and metalloids at microg g(-1) level were determined in each fraction by inductively coupled plasma optical emission spectrometry (ICP OES). Analyte concentration varied from 14 microg g(-1) (equivalent to 1.0 ng m(-3)) for As to 11.8 mg g(-1) (equivalent to 2,089 ng m(-3)) for Al. Seven elements, namely Al, Cr, Fe, Mn, Pb, Ti and Zn showed similar distributions in both seasons while As was distributed in a significantly different manner in each season. The results exhibited low As contents in the first and second fractions that could be associated with routine coal combustion and a high content in the third and fourth fractions of the summer samples that could be linked to the use of pesticides. Aluminium, As, Cu, Mn, Ni, Ti, V and Zn were found in different percentages in the more bioavailable aqueous fraction with As, Mn, V and Zn exhibiting solubilities greater than 1% while Cr and Pb being insoluble. The content of Al, Cr, Cu, Fe, Ni, Pb, and Zn in the residual fraction was, in average, higher than 50%. A comparative assessment of the use of the underlying information available from fractionation studies compared to that obtained from total element content was done for Fe and Mn. It showed that the results obtained using chemical sequential extraction procedures allowed further discrimination of the potential air pollution sources.