Heavy Metals in Moss and Bark From Urban Area of Florence: A New Cleaness Procedure for Removing Superficial Particulate Matter

Hypnum cupressiforme epiphytic moss and tree bark (elm and holm oak) samples have been collected in three sites of the city of Florence in the period 1995-1998. Lead, zinc, copper, and cadmium were determined by differential pulse anodic stripping voltammetry (DPASV) in about 200 samples collected at different heights above ground. A new clean-up procedure by nitrogen jet has been followed and its efficiency has been also verified by electron microscopy (SEM and ESEM techniques). Lead median contents in moss and bark samples fall within the ranges of 0.052-0.86 and 0.20-1.30 μmoles g^-1 (dry weight), resulting values for moss and bark are proportional to the vehicular traffic density. the increasing use of lead-free gasoline has not been followed by a decrease of lead moss concentration.     

(Persistent) Organic pollutants in Germany: results from a pilot study within the 2015 moss survey

Background

Since 1990, every 5 years, moss sampling is conducted within the European moss monitoring programme to assess the atmospheric deposition of airborne pollutants. Besides many other countries, Germany takes regularly part at these evaluations. Within the European moss monitoring 2015, more than 400 moss samples across Germany were taken according to a harmonized methodology for the assessment heavy metal and nitrogen input. In a pilot programme, eight of these sites were chosen for additional investigations on a broad range of organic contaminants to evaluate their accumulation in moss and thereby their presence in atmospheric deposition in Germany. Target compound classes comprised polycyclic aromatic hydrocarbons (PAH), polychlorinated dibenzodioxins and –furans (PCDD/F), dioxin-like and non-dioxin-like polychlorinated biphenyls (dl-PCB, ndl-PCB), polyfluorinated alkyl substances, classical flame retardants as well as emerging chlorinated and brominated flame retardants. In total, 120 target compounds were analysed. For some analytes, comparisons of accumulation in moss and tree leave samples were possible.

Results

Except for certain flame retardants, PFAS, and ndl-PCB, substances of all other compound classes could be quantified in moss samples of all sites. Concentrations were highest for PAH (40–268 ng g^?1) followed by emerging flame retardants (0.5–7.7 ng g^?1), polybrominated diphenyl ethers (PBDE; 0.3–3.7 ng g^?1), hexabromocyclododecane (HBCD; 0.3–1.2 ng g^?1), dl-PCB (0.04–0.4 ng g^?1) and PCDD/F (0.008–0.06 ng g^?1).

Conclusions

Results show the widespread atmospheric distribution and deposition of organic contaminants across Germany as well as the suitability of moss as bioaccumulation monitor for most of these compound classes. Compared to nearby tree leaf samples, accumulation potential of moss appeared to be higher for pollutants of high octanol–air partition coefficient (K_OA) and octanol–water partition coefficient (K_OW).

     

Heavy Metals in Epiphytic Mosses: An Experience in Florence

The epiphytic moss Hypnum cupressiforme has been used for passive monitoring of airborne heavy metals pollution by vehicular traffic in the urban area of Florence. Lead, cadmium, zinc and copper were determined by differential pulse anodic stripping voltammetry (DPASV). in the summer of 1993 about 30 samples were collected from the trunks of holm oak at the same height (1 metre) from the soil. Lead contents fall within the range of 0.02-1.08 μ moles g^-1 (dry weight) and for this metal, the emission source may be attributed mainly to vehicular traffic in poorly industrialized urban areas. Some evaluations have been carried out about the employment of Zn/Pb molar ratio for characterizing airborne pollution in urban areas.     

Online solid phase preconcentration using EGDMA–MAA copolymer for lead determination by FAAS

A Ethylene glycol dimethacrylate (EGDMA) methacrylic acid (MAA) resin was used for preconcentration of lead at trace levels in water samples. For this purpose, a flow-injection, solid phase extraction method was developed for the determination of lead by flame atomic absorption spectrometry. Lead ions were sorbed on a EGDMA–MAA column at pH 4, followed by an elution step using 288 µL of 4.0 M nitric acid solution and determination by flame atomic absorption spectrometry. Optimum conditions for quantitative sorption involving the pH, sample volume, loading and elution flow rates, eluent type, and volume were investigated. A 868-fold enrichment factor could be reached. The detection limit for the water samples, estimated from the noise on the signal obtained for 250 mL of 10 µg L^?1 loaded at 4.9 mL min^?1 was 1.04 µg L^?1. The method was applied for lead determination in river water samples collected in Edirne, Turkey. Recoveries of spiked solutions (10 µg L^?1) to river water samples were quantitative. Finally, the method was validated by the analysis of certified reference material SRM 2704 (Buffalo River Sediment).     

Quantification of TiO2 and ZnO nanoparticles in wastewater using inductively coupled plasma optical emission spectrometry

Abstract

The applicability of inductively coupled plasma optical emission spectrometry has been examined for determination titanium dioxide and zinc oxide nanoparticles in industrial wastewater samples. The extraction and preconcentration of the nanoparticles were achieved using ligandless ultrasound-assisted surfactant-based dispersive liquid–liquid microextraction. Under optimized conditions, the developed method had limits of detection (LOD) of 2.7?ng L^?1 for Ti and 3.6?ng L^?1 for Zn resulting from dissolved TiO₂ and ZnO nanoparticles. The relative standard deviation values for intraday precision were 2.5% and 3.1% for TiO₂ and ZnO, while the interday precision was 4.5% and 5.0%. Percentage recoveries ranging from 98% to 100% were obtained. Finally, the applicability of the method was examined by analyzing spiked samples and wastewater samples collected from textile, cosmetic and paint industries.     

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.     

Optimisation of bisphenol A removal from water using chemically modified pine bark and almond shell

The ability of pine bark and almond shells to remove bisphenol A (BPA) from aqueous solutions was evaluated. Samples of these traditional agro-forestry by-products were milled, sieved into different particle size fractions (0.10–0.15 and 1.5–2.0 mm) and submitted to two different types of treatment. Sorption experiments were conducted in a batch system at room temperature and natural pH. Sorption equilibrium was attained after 48 h for all systems under study. Bisphenol A was adsorbed more effectively on the smaller particles of the sorbents. Pine bark and almond shell pretreated with formaldehyde presented higher sorption efficiency (95%), followed by almond shell (87%) and pine bark (82%) washed with hot water. All the sorption isotherms were found to fit a Freundlich equation, with correlation coefficients (R ²) between 0.823 and 0.989. The sorption coefficient (K _F) ranged from 0.06 to 0.74 (mg^1?1/n ·L ^1/n ·g ^?1). These results indicate that utilisation of both materials as an alternative sorbent for the removal of bisphenol A from contaminated waters is promising because they are available in large amounts and have an acceptable cost–efficiency ratio when compared with traditional adsorbents.     

Human teeth as historical biomonitors of environmental and dietary lead: some lessons from isotopic studies of 19th and 20th century archival material

The lead isotopic composition of various sections (crown, crown base, root) of teeth was determined in specimens collected from 19th century skulls preserved in museum collections and, upon extraction or exfoliation, from humans of known ages residing in Scotland in the 1990s. For most 20th century samples, calculation of accurate crown-complete or root-complete dates of tooth formation ranging from the 1920s to the 1990s enabled comparison of ²⁰⁶Pb/²⁰⁷Pb ratios for teeth sections (crown base root) with corresponding decadally averaged data for archival herbarium Sphagnum moss samples. This showed that the teeth sections had been significantly influenced by incorporation of non-contemporaneous (more recent) lead subsequent to the time of tooth formation, most probably via continuous uptake by dentine. This finding confirmed that separation of enamel from dentine is necessary for the potential of teeth sections as historical biomonitors of environmental (and dietary) lead exposure at the time of tooth formation to be realised. Nevertheless, the mean 19th century value of 1.172±0.007 for the ²⁰⁶Pb/²⁰⁷Pb ratio in teeth was very similar to the corresponding mean value of 1.173±0.004 for 19th century archival moss, although relative contributions from environmental sources – whether direct, by inhalation/ingestion of dust contaminated by local lead smelting (²⁰⁶Pb/²⁰⁷Pb~1.17) and coal combustion (²⁰⁶Pb/²⁰⁷Pb~1.18) emissions, or indirect, through ingestion of similarly contaminated food – and drinking/cooking water contaminated by lead pipes of local origin, cannot readily be determined. In the 20th century, however, the much lower values of the ²⁰⁶Pb/²⁰⁷Pb ratio (range 1.100–1.166, mean 1.126±0.013, median 1.124) for the teeth collected from various age groups in the 1990s reflect the significant influence of imported Australian lead of lower ²⁰⁶Pb/²⁰⁷Pb ratio (~1.04) and released to the environment most notably through car-exhaust emissions arising from the use of alkyl lead additives (²⁰⁶Pb/²⁰⁷Pb~1.06–1.09) in petrol in the U.K. from ca. 1930 until the end of the 20th century.     

Accumulation of lead and cadmium by four tropical forage weeds found in the premises of an automobile battery manufacturing company in Nigeria

The potentials of tropical weeds namely, Nephrolepis biserrata, Panicum maximum, Eleusine indica, and Chromolaena odorata to accumulate lead (Pb) and cadmium (Cd) from soil within the premises of an automobile battery manufacturing company in Ota, south-western Nigeria, were explored. The weed samples were collected in both wet and dry seasons. Standard analytical methods were employed to collect, digest, and analyze the weeds. Lead levels in the weeds for both seasons ranged from 1990–4870, 1090–1730, 4800–7890, and 400–1210 µg g^?1 dry weight (DW) for Nephrolepis biserata, Panicum maximum, Eleusine indica, and Chromolaena odorata, respectively, while the cadmium level in the weeds for both seasons ranged from 3.92–6.78 µg g^?1 DW for N. biserata, 1.99–6.85 µg g^?1 DW for P. maximum, 2.90–7.40 µg g^?1 DW for E. indica, and 2.90–5.09 µg g^?1 DW for C. odorata. There was no significant difference in the accumulation of both Pb and Cd for the two seasons. All the weeds showed Pb levels higher than the phytotoxic range. On the contrary, 99% of the weeds showed Cd concentration within the phytotoxic range. The weeds demonstrate good phytoremediation potentials of contaminated soil.     

Determination of the levels of selected metals in seeds,flowers and fruits of medicinal plants used for tapeworm treatment in Ethiopia

The level of accumulation of selected essential and non-essential metals, namely; Ca, Cu, Fe, Zn, Mn, Cd, Pb, and Cr have been investigated in the seeds, fruits, and flowers of some medicinal plants utilized for tapeworm treatment in Ethiopia and their respective soil samples. These include seed of Cucurbita maxima (Duba), fruit of Embelia abyssinica (Ankoko), flowers of Hagenia abyssinica (Kosso), and fruits of Rosa abyssinica (Kega) and their respective soil samples. A wet digestion procedure with a mixture of conc. HNO₃ and HClO₄ for the plant samples and a mixture of conc. HNO₃, HCl, and H₂O₂ for soil samples were used to solubilize the metals. Ca (1280–12,670?mg?kg^?1) was the predominant metal followed by Fe (104–420?mg?kg^?1), and Zn (18–185?mg?kg^?1) in all the plant materials except for Hagenia abyssinica flower from Hirna in which Mn (16–42?mg?kg^?1) followed by Fe. Among the non-essential toxic metals, Pb was not detected in Cucurbita maxima of Boji, Gedo and Hirna origins and in Rosa abyssinica of Hirna site. Similarly, Cr was not detected in Rosa abyssinica fruits of Boji and Gedo sites. The sampled soils were found to be between strongly acidic to weakly basic (pH: 4.7–7.1). In the soil samples, Ca (8528–18,900?mg?kg^?1) was the most abundant metal followed by Fe (417–912?mg?kg^?1), Zn (155–588?mg?kg^?1), Mn (54–220?mg?kg^?1), Cr (21–105. mg?kg^?1), Cu (11–58?mg?kg^?1), Pb (13–32?mg?kg^?1) and Cd (2.8–4.8?mg?kg^?1). The levels of most of the metals determined in the medicinal plants and the respective soil samples are in good agreement with those reported in the literature and the standards set for the soil by various legislative authorities.     

Addendum

Bags of S. auriculatum and a low‐volume aerosol sampler with filters were exposed, in parallel, to the urban atmosphere of Oporto at four sampling points and for about two months periods, between 1991 and 1994. The levels of lead in the moss (weekly samples) and in the filters (daily samples) were determined by atomic absorption spectrophotometry and the results were compared. In dry weather periods (relative humidity ≤ 76%) the rate of lead uptake by moss was approximately constant and proportional to the levels of the metal in atmospheric aerosols. A converting factor (CF = lPb_moss l (μg/g.day)/ l Pb_air l (μg/m³)) allowed conversion of the lead levels in S. auriculatum to those in the atmospheric aerosols. Because the moss fixed lead from gas, aerosol and particulated matter, the rate of sorption depends markedly on the distance to the lead sources (traffic) and on surrounding obstacles which retain particles. Therefore, specific calibration by mechanic monitoring at each point of sampling is required when moss bag samplers are used to provide quantitative information about lead levels in the atmosphere. In wet weather periods, higher but irregular rate of lead uptake was observed. In contrast, the lead levels in atmospheric aerosols decreased when the humidity increased due to wet deposition. Therefore, no proportionality between the lead levels in the moss and in the air were found.     

Potential correlation between perfluorinated acids and liver morphology in East Greenland polar bears (Ursus maritimus)

In this study, residual concentrations of chlorpyrifos (CPF) were determined in feed (40) and fodder (25) samples collected from various locations of Tarai region of Uttarakhand. For extracting residues, liquid–liquid partition followed by alumina column clean up was used and the detection and quantification of residues was undertaken with the help of high-performance liquid chromatography using C18 column and diode array detector at 220?nm. Of the total 40 feed samples analyzed, 7 (17.5%) samples were found positive for CPF with the mean residual concentration of 0.058?µg?g^?1; while out of 25 fodder samples, CPF residues were detected in a single (4%) sample with residual concentration of 0.39?µg?g^?1. However, none of the feed or fodder samples contained CPF residues above the prescribed limit.     

Vehicle-Induced Lead and Cadmium Contamination of Roadside Soil and Plants in Italy

Lead and cadmium concentrations in spontaneous vegetation and in soil sampled at various distances (0–208 m) from several motorways throughout Italy were measured. Lead and cadmium concentrations appear to be correlated to distance from the motorway and to traffic levels. A comparison with data from a remote and unpolluted site shows that foliar lead concentrations can be up to 40 times higher, and foliar cadmium concentrations up to 3 times higher. Plants behave differently in their accumulation of lead and cadmium; conifers present the highest levels. Also the various receptors and compartments of the roadside ecosystem differ in their accumulation of lead and cadmium; soil and bark have consistently higher concentrations, while the leaves and twigs of trees have consistently lower levels. the data recorded by ad hoc introduced bio-accumulating plants (Lolium multiflorum L.) are consistent with those of the spontaneous vegetation. the concentrations of both lead and cadmium in Lolium vary from June to November, following in part the fluctuation in traffic density.     

Monoterpene chemodiversity of ponderosa pine in relation to herbivory and bark beetle colonization

Summary. Ponderosa pine, Pinus ponderosa Laws. (Pinaceae), forests in Arizona have suffered from a nine-year period of drought and bark beetle, Ips lecontei Swaine (Coleoptera: Scolytidae), outbreaks. Abiotic and biotic stress in ponderosa pine results in the induced synthesis of certain monoterpenes that may in turn affect bark beetle behavior and survival. In this study, we investigate whether induced monoterpene production could result in a different monoterpene composition that remains stored in the needles or the trunk resin of the tree. Needle and resin samples in addition to trunk cores were collected from ponderosa pines at three locations in Arizona. Ungulate browsing induced a significant increase in limonene (P=0.010) and in chemodiversity (P=0.009), a measure of the evenness of distribution among the monoterpenes present in needles. We compared the level of ‘stress’ of the trees by measuring the thickness of annual rings in living trees and those that were killed by bark beetles. Where drought occurred, the spacing of annual rings from the last 10 years of trees killed by bark beetles was significantly smaller (P=0.020) compared to living trees. There was no difference in the monoterpene composition between the core sections of closest spacing of annual rings (stressed years) compared to the sections of widest spacing, which indicates that monoterpenes are distributed evenly throughout the extended resin system. In the area where the degree of drought was less overall, none of the individual monoterpenes present in the resin was related to bark beetle killed trees. However, about half the living pines had resin in which one of the major monoterpenes (α-pinene, Δ³-carene, and limonene) was absent, and these trees had a lower monoterpene chemodiversity compared to trees killed by bark beetles. Trees with these three major monoterpenes, corresponding to the average relative proportion in living pines at that location, may sustain higher selection and colonization by bark beetles.     

Assessment of metals in soil extracts and their uptake and movement within Tamarix nilotica at Lake Nasser banks,Egypt

This study aims to determine heavy-metal levels in soil from the banks of Lake Nasser, the ability of Tamarix nilotica to accumulate such metals from soil and hence its potential for phytoextraction. Soil and Tamarix samples were collected from the banks of four bights around Lake Nasser and analysed for Fe, Mn, Ca, Mg, Cr, Cu, Ni, Zn, Cd and Pb by atomic absorption spectrometry, whereas Na and K were measured by atomic emission spectrophotometry. Three different methods of extraction were used for the soil samples. Lead, copper and zinc were equally distributed between the exchangeable phase and Fe/Mn oxide-bound form, while other measured metals were mainly present in the Fe/Mn oxide fraction. With the exception of iron, all metals studied showed total concentrations within the geochemical background values. T. nilotica exhibited elevated concentrations of Na (36.2–48.5?mg?g^?1) and K (2.74–4.33?mg?g^?1) in stems, and relatively high concentrations of Pb, Cd and Co (0.39–1.03?µg?g^?1, 0.24–1.3?µg?g^?1 and 1.94–5.3?µg?g^?1, respectively) are found in plant leaves. Bioaccumulation factors of Na and K (9.3 and 12.63, respectively) were high in T. nilotica stems. While the bioaccumulation of Pb, Cd, Co and Ni (2870.1, 2035.4, 10.5 and 5313.2, respectively) was high in plant leaves, Fe, Mn, Ca and Mg were accumulated relatively equally in plant stems and leaves. T. nilotica was found to secrete high amounts of Na, Ca and K, in addition to small amounts of all accumulated metals except Cd and Cu. These secreted metals appeared as salt crystals (67.5% Na; 25.8% Ca; 5% Mg; 1.5% K and 0.16% trace and minor elements) on the plant surface. The concentrations of all the metals studied in T. nilotica were higher than in the salt crystals. Statistical analysis of the database suggests bioaccumulation of these metals from soil to T. nilotica. This reflects the importance of using T. nilotica as a model in the phytoremediation process as an established environmental clean-up technology.     

Levels and distribution of trace metals in surface sediments from Kongsfjorden, Svalbard, Norwegian Arctic

Trace metal contents (Cd, Co, Cr, Cu, Hg, Mn, Ni, Pb and Zn) have been measured in 27 surface sediment samples collected from Kongsfjorden, Svalbard, Norwegian Arctic. The analyses yielded concentration values (in mg kg^?1) of 0.13–0.63 for Cd, 11.89–21.90 for Co, 48.65–81.84 for Cr, 21.26–36.60 for Cu, 299.59–683.48 for Mn, 22.43–35.39 for Ni, 10.68–36.59 for Pb, 50.28–199.07 for Zn and 8.09–65.34 for Hg (in ng g^?1), respectively. Relative cumulative frequency method has been used to define the baseline values of these metals, which (in mg kg^?1) were 0.14 for Cd, 13.56 for Co, 57.86 for Cr, 25.14 for Cu, 364.08 for Mn, 26.22 for Ni, 17.46 for Pb, 70.49 for Zn and 9.76 for Hg (in ng g^?1), respectively. The enrichment factor analysis indicated that Hg showed some extent of anthropogenic pollution, while Pb, Zn and Cd showed limited anthropogenic contamination in the study areas.     

Risk assessment of children's blood lead level in some rural habitations of western Uttar Pradesh,India

The objective of this study was to determine the blood lead level (BLL) of children aged under 5 living in western Uttar Pradesh, India. A total of 100 blood samples, 100 drinking water samples, and 21 vegetable samples were assessed for lead (Pb) contamination. BLL was observed in the range of 3–11.58?µg?dL^?1 with a maximal level of 11.58?±?0.05?µg?dL^?1 in Kazipur village. Lead in water samples was detected in the range of 0.006–0.095?ppm and identified at upto 9.5-fold higher than the stated permissible limit. A significant positive correlation (+0.679) was obtained between BLL and water Pb levels. All vegetable samples were also contaminated with Pb upto 12-fold higher than the permissible limit of 2.5?µg?g^?1 of Prevention of Food Adulteration Act (PFA) 1954. Untreated industrial effluents were identified as the responsible factors for Pb occurrence in the study area. The presence of lead may be associated with the increased antisocial activities of children living in western Uttar Pradesh. Children with elevated BLL had poorer nutritional status than those with background Pb levels. There is an urgent need for a national campaign to monitor the BLL of children in India.     

The role of sample preparation in interpretation of trace element concentration variability in moss bioindication studies

Trace element concentrations in plant bioindicators are often determined to assess the quality of the environment. Instrumental methods used for trace element determination require digestion of samples. There are different methods of sample preparation for trace element analysis, and the selection of the best method should be fitted for the purpose of a study. Our hypothesis is that the method of sample preparation is important for interpretation of the results. Here we compare the results of 36 element determinations performed by ICP-MS on ashed and on acid-digested (HNO₃, H₂O₂) samples of two moss species (Hylocomium splendens and Pleurozium schreberi) collected in Alaska and in south-central Poland. We found that dry ashing of the moss samples prior to analysis resulted in considerably lower detection limits of all the elements examined. We also show that this sample preparation technique facilitated the determination of interregional and interspecies differences in the chemistry of trace elements. Compared to the Polish mosses, the Alaskan mosses displayed more positive correlations of the major rock-forming elements with ash content, reflecting those elements’ geogenic origin. Of the two moss species, P. schreberi from both Alaska and Poland was also highlighted by a larger number of positive element pair correlations. The cluster analysis suggests that the more uniform element distribution pattern of the Polish mosses primarily reflects regional air pollution sources. Our study has shown that the method of sample preparation is an important factor in statistical interpretation of the results of trace element determinations.     

Determination of cobalt by air-assisted liquid–liquid microextraction

Abstract

A rapid and selective technique for extraction, preconcentration and determination of trace amounts of cobalt in water and pharmaceutical samples by air-assisted liquid–liquid microextraction combined with flame atomic absorption spectrometry is proposed. 1-Nitroso-2-naphthol is used as a complexing agent and 1-octanol as an extraction solvent. Parameters relevant for analytical effectivity, i.e. pH of sample solution, concentration of complexing agent, volume of extraction solvent, and number of extraction cycles are optimized using a Box–Behnken design. At optimum conditions, a dynamic linear range of 5–600?µg L^?1 is obtained, with a limit of detection of 1.2?µg L^?1. The method is used for determination of Co(II) in environmental water and pharmaceutical samples.     

Distribution patterns of lead in urban soil and dust in Shenyang city, Northeast China

We investigated the spatial distribution of Pb in soil and dust samples collected from 54 sites in Shenyang city, Liaoning province, Northeast China. Soil background Pb concentration was 22 mg kg⁻¹ and control values from non-industrial areas were 33 mg kg⁻¹ for soil and 38 mg kg⁻¹ for dust. Soil Pb concentrations varied widely, ranging from 26 to 2911 mg kg⁻¹, with a mean concentration of 200 mg kg⁻¹, 9 times the background value and 6 times the control value. There was great variation in soil Pb, with a coefficient of variation (CV) of 1.06 and a standard deviation (SD) of 212 mg kg⁻¹. Dust Pb concentrations fluctuated from 20 to 2810 mg kg⁻¹, with a mean value of 220 mg kg⁻¹, almost 6 times the control value. No significant differences in distribution were observed between soil Pb and dust Pb. The highest Pb concentration was observed in Tiexi district in an industrial area. Soil Pb concentration decreased with depth and with distance from the pollution source. Lead concentrations initially changed little but then decreased with distance from the roadside, and were generally higher on the east side of roads than on the west. Lead contents in different categories of urban area differed substantially with dust and soil Pb concentrations decreasing in the sequence: industrial >business >mixed (residential, culture and education)> reference areas.