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1.
In this research, we have investigated the removal efficiency of natural organic matter (NOM) from river and stream water using potassium ferrate(VI). For the study, ferrate was added in 100-ml water sample mixed either with humic acid or with fulvic acid. The removal efficiency at the ferrate dose of 2–46 mg/l (as Fe) was 21–74% for 10 mg/l humic acid and 48–78% for 10 mg/l fulvic acid. NOM was more effectively removed either at lower pH or at higher temperature. The removal performance by ferrate was comparable to that by traditional coagulants (i.e., alum, FeSO4·7H2O, and FeO(OH)). In addition, the removal rate of humic acid using traditional coagulants was improved by pretreatment with a very small dose of ferrate. The reaction between ferrate and humic acid was completed within 60 s, while showing first-order kinetic, and then reached a steady state.  相似文献   

2.
Metal (Cu, Mn, Ni, Zn, Fe) concentrations in marine sediment and zooplankton were investigated in Izmir Bay of the Eastern Aegean Sea, Turkey. The study aimed to assess the levels of metal in different environmental compartments of the Izmir Bay. Metal concentrations in the sediment (dry weight) ranged between 4.26–70.8 μg g?1 for Cu, 233–923 μg g?1 for Mn, 14.9–127 μg g?1 for Ni, 25.6–295 μg g?1 for Zn, 12,404–76,899 μg g?1 for Fe and 38,226–91,532 μg g?1 for Al in the Izmir Bay. Maximum metal concentrations in zooplankton were observed during summer season in the inner bay. Significant relationships existed between the concentrations of certain metals (Al, Fe, Mn and Ni) in sediment, suggesting similar sources and/or similar geochemical processes controlling such metals. Higher concentrations of Cu, Zn and percent organic matter contents were found in the middle-inner bays sediments. Based on the correlation matrix obtained for metal data, organic matter was found to be the dominant factor controlling Cu and Zn distributions in the sediment. In general, mean Cu and Zn levels in the bay were above background concentrations in Mediterranean sediments. Zooplankton metal concentrations were similar to sediment distributions.  相似文献   

3.
Spatial and seasonal mobilization trends of metals in surface water were evaluated in the US–Mexico San Pedro River (SPR). Water samples were collected at five sampling stations for the analysis of dissolved oxygen, pH, electric conductivity, sulfates, and metals (Cd, Cu, Fe, Mn, Pb, and Zn). Quality of the water was characterized through Ecological Criteria of Water Quality (ECWQ) established in Mexico and Water Quality Criteria (Environmental Protection Agency (EPA)). High total metal concentrations were detected as follows: Fe?>?Cu?>?Mn?>?Zn?>?Pb?>?Cd. Metal concentrations were slightly higher in dry season than in rainy season: Cd (below detection limit (BDL)–0.21 mg L?1), Cu (BDL–13 mg L?1), Fe (0.16–345 mg L?1), Mn (0.12–52 mg L?1), Pb (BDL–0.48 mg L?1), and Zn (0.03–17.8 mg L?1). Low pH and dissolved oxygen values as well as high sulfate content were detected in both seasons. High values of metals (Cd, Cu, Fe, Mn, Pb, Zn) were detected at station E1 representing pollution source, as well as at stations E2 (Cd, Cu, Fe, Mn), E3 (Fe, Mn, Pb), and E4 and E5 (Fe, Mn). Detected concentrations exceeded maximum permissible established in ECWQ and Water Quality Criteria (EPA). Efflorescence salts on sediments in the dry season could increase levels of metals in water column. This study provides valuable information on the potential mobility of metals in surface water of SPR located in an arid environment where transport processes are strongly linked to climate. The information derived from this study should help the regional and national authorities to address present environmental regulations.  相似文献   

4.
Abstract

Long‐term agricultural sustainability and water quality are impacted by different chemicals, including heavy metals. Heavy‐metal losses at the catchment scale depend largely on land‐management practices. Water‐quality indicators are required near soil‐quality indicators for different regions and farming systems. The purpose of this work is to analyze the heavy‐metal losses from a mixed agroforestry catchment. Iron (Fe), Magnesium (Mn), Zinc (Zn), and Copper (Cu) were measured in the drainage water of a 36.3 km2 catchment located at the Valiñas River (Coruña, northwest Spain), and a total of 193 samples were collected during the course of 2003. The sampling strategy was a stratified point sampling involving more frequent sampling when flow was high. Water metal content was analyzed by inductively coupled plasma (ICP‐AES). The content ranges of dissolved heavy metals were as follows: Fe between 10 and 267 µg/L, Mn 0.2 and 77 µg/L, Zn 0.62 and 53.7 µg/L, and Cu 0.20 and 9.26 µg/L. Heavy metal content strongly varied along the study time, depending on storm flow but also on timing of animal‐waste applications.  相似文献   

5.
The relationships between heavy metal concentrations and physico-chemical properties of natural lake waters and also with chemical fractions of these metals in lake sediments were investigated in seven natural lakes of Kumaun region of Uttarakhand Province of India during 2003–2004 and 2004–2005. The concentrations of Cr, Mn, Fe, Ni, Cu, Zn, Cd and Pb in waters of different lakes ranged from 0.29–2.39, 10.3–38.3, 431–1407, 1.0–6.6, 5.3–12.1, 12.6–166.3, 0.7–2.7 and 3.9–27.1 μg l?1 and in sediments 14.3–21.5, 90.1–197.5, 5,265–6,428, 17.7–45.9, 13.4–32.0, 40.0–149.2, 11.1–14.6 and 88.9–167.4 μg g?1, respectively. The concentrations of all metals except Fe in waters were found well below the notified toxic limits. The concentrations of Cr, Mn, Ni, Cu, Zn, Cd and Pb were positively correlated with pH, electrical conductivity, biological oxygen demand, chemical oxygen demand and alkalinity of waters, but negatively correlated with dissolved oxygen. The concentrations of Cr, Ni, Zn, Cd and Pb in waters were positively correlated with water soluble + exchangeable fraction of these metals in lake sediments. The concentrations of Zn, Cd and Pb in waters were positively correlated with carbonate bound fraction of these metals in lake sediments. Except for Ni, Zn and Cd, the concentrations of rest of the heavy metals in waters were positively correlated with organically bound fraction of these metals in lake sediments. The concentrations of Cr, Mn, Ni, Cu and Zn in waters were positively correlated with reducible fraction of these metals in lake sediments. Except for Cd, the concentrations of rest of the metals in waters were positively correlated with residual fraction and total content of these heavy metals in lake sediments.  相似文献   

6.
Abstract

Three different chemical extractants were evaluated as to their extraction efficiency for copper (Cu), zinc (Zn), lead (Pb), aluminium (Al), iron (Fe), chromium (Cr), manganese (Mn), potassium (K), magnesium (Mg), and calcium (Ca) on forest soil profiles from the Romanian Carpathians. The extractants were hot 14 M nitric acid (HNO3), 0.05 M hydrochloric acid (HCl), and 0.1 M sodium pyrophosphate. By comparing amounts extracted by 0.05 M HCl and 0.1 M sodium pyrophosphate relative to that dissolved by hot 14 M HNO3, some conclusions were drawn concerning the chemical forms of the metals in the extractable pool. The amount released by 0.05 M HCl was generally less than 10% of the HNO3‐extractable fraction but showed considerable variation among the elements studied. The relative amount extracted by pyrophosphate increased with organic‐matter content of the soils for Cu, Zn, Pb, Al, Fe, and Cr; stayed more or less constant for Mn, K, and Mg; and decreased for Ca. These findings are discussed with respect to the different binding forms of the metals in the soil and the processes affecting their mobility. From the present results, the metals were ranked as follows with respect to their ability to form organic complexes in natural soils: Cu>Cr, Pb>Ca>Al>Fe, Zn, Mn, K>Mg. However, the use of cold dilute HCl as a fractionation step may be questionable in cases of soils with a high content of substances possessing large neutralization capacity for protons.  相似文献   

7.
Freshly deposited stream sediments from six urban centres of the Ganga Plain were collected and analysed for heavy metals to obtain a general scenery of sediment quality. The concentrations of heavy metals varied within a wide range for Cr (115–817), Mn (440–1 750), Fe (28 700–61 100), Co (11.7–29.0), Ni (35–538), Cu (33–1 204), Zn (90–1 974), Pb (14–856) and Cd (0.14–114.8) in mg kg-1. Metal enrichment factors for the stream sediments were <1.5 for Mn, Fe and Co; 1.5–4.1 for Cr, Ni, Cu, Zn and Pb; and 34 for Cd. The anthropogenic source in metals concentrations contributes to 59% Cr, 49% Cu, 52% Zn, 51% Pb and 77% Cd. High positive correlation between concentrations of Cr/Ni, Cr/Cu, Cr/Zn, Ni/Zn, Ni/Cu, Cu/Zn, Cu/Cd, Cu/Pb, Fe/Co, Mn/Co, Zn/Cd, Zn/Pb and Cd/Pb indicate either their common urban origin or their common sink in the stream sediments. The binding capacity of selected metals to sediment carbon and sulphur decreases in order of Zn > Cu > Cr > Ni and Cu > Zn > Cr > Ni, respectively. Stream sediments from Lucknow, Kanpur, Delhi and Agra urban centres have been classified by the proposed Sediment Pollution Index as highly polluted to dangerous sediments. Heavy metal analysis in the <20-μm-fraction of stream sediments appears to be an adequate method for the environmental assessment of urbanisation activities on alluvial rivers. The present study reveals that urban centres act as sources of Cr, Ni, Cu, Zn, Pb and Cd and cause metallic sediment pollution in rivers of the Ganga Plain.  相似文献   

8.
This paper presents a comparative study of the performance of ferrate(VI), FeO 4 2? , and ferric, Fe(III), towards wastewater treatment. The ferrate(VI) was produced by electrochemical synthesis, using steel electrodes in a 16 M NaOH solution. Domestic wastewater collected from Hailsham North Wastewater Treatment Works was treated with ferrate(VI) and ferric sulphate (Fe(III)). Samples were analysed for suspended solids, chemical oxygen demand (COD), biochemical oxygen demand (BOD) and P removal. Results for low doses of Fe(VI) were validated via a reproducibility study. Removal of phosphorous reached 40% with a Fe(VI) dose as low as 0.01 mg/L compared to 25% removal with 10 mg/L of Fe(III). For lower doses (<1 mg/L as Fe), Fe(VI) can achieve between 60% and 80% removals of SS and COD, but Fe(III) performed even not as well as the control sample where no iron chemical was dosed. The ferrate solution was found to be stable for a maximum of 50 min, beyond which Fe(VI) is reduced to less oxidant species. This provided the maximum allowed storage time of the electrochemically produced ferrate(VI) solution. Results demonstrated that low addition of ferrate(VI) leads to good removal of P, BOD, COD and suspended solids from wastewater compared to ferric addition and further studies could bring an optimisation of the dosage and treatment.  相似文献   

9.
This study determines the seasonal variability of metal partition coefficients [aluminium (Al), iron (Fe), manganese (Mn), copper (Cu), and zinc (Zn)] and analyses the importance of suspended sediments (SS), dissolved organic carbon (DOC) concentrations, pH, and discharge (Q) on the seasonal variability of metal partition coefficients (KDs) in the headwaters of the Mero River catchment, which drains an agroforestry area in northwestern Spain. Metal partition coefficients were used as an approach to relate dissolved and particulate fractions. Water samples were collected over 3 years (2005–2008) at the catchment outlet. The mean metal dissolved concentrations were: Fe (43.5 μg L?1) > Al (23.3 μg L?1) > Zn (1.8 μg L?1) > Mn (1.2 μg L?1) > Cu (0.3 μg L?1). Partition coefficients followed the order Mn > Al > Fe > Zn > Cu, and their values exhibited low variability. Al, Cu, and Zn partition coefficients presented the greatest values in summer, except during 2007–2008, when the greatest KDs value was observed in autumn, whereas the KDs of Fe showed the greatest values in winter. The KD of Mn has no seasonality. For Al, Cu, and Zn, the seasonal SS concentrations were closely related to Kd. For Fe, Kd was more closely related to DOC concentration than to SS concentration.  相似文献   

10.
The assessment of heavy metals in spinach (Spinacia oleracea) grown in sewage sludge–amended soil was investigated. The results revealed that sewage sludge significantly (P < 0.01) increased the nutrients and heavy metals such as cadmium (Cd), chromium (Cr), copper (Cu), manganese (Mn), and zinc (Zn) in the soil. The contents of metals were found to be below the maximum levels permitted for soils in India. The most agronomic performance and biochemical components of S. oleracea were found at 50% concentrations of sewage sludge in both seasons. The contents of Cd, Cr, Cu, Mn, and Zn in S. oleracea were increased from 5% to 100% concentrations of sewage sludge in both seasons. The order of contamination factor (Cf) of different heavy metals was Mn > Cd > Cr > Zn > Cu for soil and Cr > Cd > Mn > Zn > Cu for S. oleracea plants after application of sewage sludge. Therefore, use of sewage sludge increased concentrations of heavy metals in soil and S. oleracea.  相似文献   

11.
Edible muscle tissues of Solea solea, Mullus barbatus, and Sardina pilchardus marketed in Mersin were analyzed for their Cr (total), Mn, Fe, Ni, Cu, Zn, As (total), Cd, Sn, and Pb levels. Metal levels of the tissues were determined using inductively coupled plasma-mass spectrophotometric (ICP-MS) methods. Muscle levels of Cr, Mn, Fe, Ni, Cu, Zn, As, Sn, and Pb were determined as 0.19–2.80, 0.08–3.88, 0.93–25.76, 0.03–0.63, 0.01–1.96, 1.28–45.95, 0.49–25.26, 0.14–4.03, and 0.02–1.37 mg kg?1 w.w., respectively. Cadmium levels were below detection limits in all the muscle samples taken. Mean metal levels of the tissues were compared with the provisional tolerable daily (PTDs) and weekly (PTWIs) intake limits. Mean metal levels taken by the consumption of analyzed tissues were below PTDs and PTWIs; hence, the fish species studied do not pose any risk for human consumption from the point of heavy metals.  相似文献   

12.
In the present study, a laboratory experiment was designed to compare the 0.01 M calcium chloride (CaCl2) and diethylenetriaminepentaacetic acid (DTPA) extraction methods for their ability to predict cadmium (Cd), copper (Cu), iron (Fe), Manganese (Mn), nickel (Ni), and zinc (Zn) availability and mobility in five calcareous soils. The soils were spiked with different amounts of metals (0, 50, 100, 200, and 400 mg kg?1) both in binary (Cu and Zn; Ni and Cd; Fe and Mn) and in multi-systems (Cd, Cu, Fe, Mn, Ni, and Zn) and incubated for 1 months at field capacity. In metal-spiked soils, both extraction methods showed a linear relationship of extractable to total metals for all soils. The fraction of total metals extracted by DTPA was much higher than the fraction extracted by CaCl2, which was attributed to the formation of soluble metal-complexes in the complexing extracts calculated by the Visual Minteq program. DTPA extraction method showed higher selectivity for Cu over other metals both in binary and in multi-systems. Different order of metals extractability was found in binary and multi-systems for both extraction methods. Solid/solution distribution coefficient (Kd) was calculated by the ratio of the solid phase to soil solution concentration of metals extracted by CaCl2 or DTPA extraction methods. Both in binary and in multi-systems, the average Kd (l kg?1) of metals by soils were in the order of Mn (5398) > Fe (4413) > Zn (3376) > Cu (2520) > Ni (969) > Cd (350) in the CaCl2-extractable metals and Fe (35) ≥ Ni (34) > Zn (18) > Mn (11.2) > Cu (6.3) > Cd (4) in the DTPA-extractable metals. Results showed that among the six studied metals, Cd had the lowest Kd, implying a relative higher mobility in these calcareous soils. The Visual Minteq indicated that in the CaCl2-extraction method and in both binary and multi-systems the dominant species for Cu, Mn, Ni, and Zn were Cu2+, Mn2+, Ni2+ and Zn2+, respectively, while for Cd and Fe, the dominant species were CdCl+ and Fe(OH)2+, respectively.  相似文献   

13.
Chemical speciation and bioaccumulation factor of iron (Fe), manganese (Mn), and zinc (Zn) were investigated in the fractionated rhizosphere soils and tissues of sunflower plants grown in a humic Andosol. The experiment was conducted for a period of 35 days in the greenhouse, and at harvest the soil system was differentiated into bulk, rhizosphere, and rhizoplane soils based on the collection of root-attaching soil aggregates. The chemical speciations of heavy metals in the soil samples were determined after extraction sequentially into fractions classified as exchangeable, carbonate bound, metal–organic complex bound, easily reducible metal oxide bound, hydrogen peroxide (H2O2)–extractable organically bound, amorphous mineral colloid bound, and crystalline Fe oxide bound. Iron and Zn were predominantly crystalline Fe oxide bound in the initial bulk soils whereas Mn was mainly organically bound. Heavy metals in the exchangeable form accumulated in the rhizosphere and rhizoplane soils, comprising <4% of the total content, suggesting their relatively low availability in humic Andosol. Concentrations of organically bound Fe and Mn in soils decreased with the proximity to roots, suggesting that organic fraction is the main source for plant uptake. Concentrations of Mn and Zn in the metal–organic complex also decreased, indicating a greater ability of sunflower to access Mn from more soil pools. Sunflower showed bioaccumulation factors for Zn, Fe, and Mn as large as 0.39, 0.05, and 0.04 respectively, defining the plant as a metal excluder species. This result suggests that access to multiple metal pools in soil is not necessarily a major factor that governs metal accumulation in the plant.  相似文献   

14.
Abstract

The effect of bacterial inoculation of Rhizobium fredii HN01 on the immobilization and speciation of Cu, Zn, and Cd was studied in Red and Cinnamon soil which are typical Chinese soils. The soil was mixed with bacterial suspension for one week followed by an immobilization of each heavy metal for another week. The total binding and fractionation of heavy metals in soils were analyzed. As compared with the control, the retention of total Cu, Zn, and Cd in Red soil increased by 28, 16, and 28%, respectively, in the presence of rhizobia. The amount of exchangeable, NH4OAc-extractable, Mn oxides-bound and organic matter-bound Cu increased by 23–123%. There were significant decrease of exchangeable Cu and marked increases of NH4OAc-extractable and Mn oxide-bound Cu in Cinnamon soil with the presence of rhizobial cells, although no changes for the total retention of Cu were observed. The amount of exchangeable Zn in Red soil-rhizobia composite was 20% greater than that of the no-rhizobia soil. Addition of rhizobia also increased exchangeable Cd and specifically-adsorbed Cd by 25 and 93%, respectively, in Red soil. No considerable differences were found for the total immobilization of Zn and Cd as well as their distribution in various solid fractions of Cinnamon soil in the absence and presence of rhizobial cells. In terms of soil components, it is assumed that bacterial biomass had a relatively less impact on the species of heavy metals bound with Fe oxides. Results suggested that the retention and speciation of heavy metals in soil are governed largely by the interactions of bacteria with various inorganic and organic soil constituents. The data are useful in understanding the impact of microorganisms on the behavior, mobility and transformation of heavy metals in soil environments.  相似文献   

15.
Heavy metal transport in Cauvery river chiefly takes place in the particulate form. Tributaries Hemevathi and Kabini draining highly mineralized areas contribute significantly to the heavy metal load of the Cauvery river. Particulate metal transport is influenced by the presence of major dams built across the river. Factor analysis of the elemental data identifies two major group of heavy metals, (a) Fe, Mn, Cr, V and Ti and (b) Cu, Pb and Zn in the suspended sediments of Cauvery river. Heavy metals in surface sediments show wide variations in their concentrations due to the non-uniform grain size distribution of the sediments. The elements Fe, Mn, Pb, Cu, Zn, Ni, Co and As are dominantly present in the <20 μm fraction of the river sediments. Speciation studies show that Fe-Mn oxide phase held the largest share of heavy metals in the sediments. The depth variation of heavy metals in the core sediments suggest their similar mobility during diagenesis. Geoaccumulation indices calculated suggest that Cd, Zn, Cr, Pb, Cu and Ni are enriched in sediments several times over background values.  相似文献   

16.
The risk assessment of heavy‐metal contamination in soils requires knowledge of the controls of metal concentrations and speciation. We tested the relationship between soil properties (pH, CEC, Corg, oxide concentrations, texture) and land use (forest, grassland, arable) and the partitioning of Al, Cd, Cr, Cu, Fe, Mn, Ni, Pb, and Zn among the seven fractions of a sequential extraction procedure in 146 A horizons from Slovakia. Using a cluster analysis, we identified 92 soils as representing background metal concentrations while the remaining 54 soils showed anthropogenic contamination. Among the background soils, forest soils had the lowest heavy‐metal concentrations except for Pb (highest), because of the shielding effect of the organic layer. Arable soils had the highest Cr, Cu, and Ni concentrations suggesting metal input with agrochemicals. Grassland soils had the highest Cd and Zn concentrations probably for geogenic reasons. Besides the parent material (highest metal concentrations in soils from carbonatic rock, lowest in quartz‐rich soils with sandy texture), pedogenic eluviation processes controlled metal concentrations with podzols showing depletion of most metals in E horizons. Partitioning among the seven fractions of the sequential extraction procedure was element‐specific. The pH was the overwhelming control of the contributions of the bioavailable fractions (fractions 1–4) of all metals and even influenced the contributions of Fe oxide‐associated metals (fractions 5 and 6) to total metal concentrations. For fractions 5 and 6, Fe concentrations in oxides were the most important control of contributions to total metal concentrations. After statistically separating the pH from land use, we found that the contributions of Cu in fractions 1–4 and of NH4NO3‐extractable Al, Cd, Pb, and Zn to total metal concentrations were significantly higher under forest than under grassland and in some cases arable use. Our results confirm that metal speciation in soils is mainly controlled by the pH. Furthermore, land use has a significant effect.  相似文献   

17.
Rain is a main source for getting water to the ecosystem in the Indian continent. The factors i.e. operation of several heavy metal industries, coming of distant pollutants, high rain fall, etc. are agent for the precipitation of a high amount of the heavy metals in the eastern region of Madhya Pradesh state of India. The particulate matters and gases emitted are scavenged out with rain water for the distribution to the ecosystem. 216 event rain water samples were collected at three sites (representative of urban, industrial and remote): Raipur, Korba and Ambikapur of the country in the year 1995. 60 (30×2) event samples were collected at site Raipur during years, 1996–1997. The volume weighted mean concentration and fluxes distribution of most abundant heavy metals i.e. Mn, Fe, Cu, Zn, Hg, Pb are described. Their concentration level found in the rain water was: Pb?Zn?Cu?Fe>Mn?Hg.  相似文献   

18.
Abstract

Soils under the main mangrove (Rhizophora racemosa and Avicennia germinans) forest in the Niger Delta, Nigeria, were characterized, and their capacities to retain heavy metals were examined by using soil column leaching experiments, using 20 mg L?1 Cu, 50 mg L?1 Zn, 20 mg L?1 Cd, and 100 mg L?1 Mn solutions. At the end of the leaching experiments, soil samples from each column were divided into two layers (0–5 cm and 5–10 cm) and analyzed for total metal retained. The fractionation of heavy metals in the surface soil samples (0–5 cm) was investigated by the sequential extraction technique. The study showed that the soils were influenced by tidal flow and characterized by the presence of very fine textured, thin (0–5 cm) to moderately thick (10–15 cm) layer of alluvium (mud) on the surface. The fibric soil material beneath the surface mud varies in thickness from about 70 to 100 cm, and beyond the histic layer is the plastic, very sticky, massive clay. In situ, the soils were neutral in reaction (pH 7.0–7.2), but became strongly acid (pH 3.3–4.8) upon drying. They are saline, high in soluble salts, highly reduced, with CEC that is low in the fibric layer, but high in the mineral, clayey subsoil horizon. The soils are saturated with water for much more than 30 days in a year and have fiber content that is more than 40 cm thick, with the fibric sphagnum constituting more than three‐fourths by volume to a depth greater than 90 cm. The soils, classified as Typic Sphagnofibrists, sequestered considerable amounts of copper (Cu), zinc (Zn), cadmium (Cd), and manganese (Mn) with most of the metals retained in the surface soils. The anthropogenic heavy metals were mostly adsorbed probably to the negatively charged sites of organics and clay. These loosely bound metals may be desorbed and reenter the aqueous phase, thus becoming a secondary source of metal pollution.  相似文献   

19.
Total Suspended particulate matter (TSP) in urban atmosphere of Islamabad was collected using a high volume sampling technique for a period of one year. The nitric acid–perchloric acid extraction method was used and the metal contents were estimated by atomic absorption spectrophotometer. The highest mean concentration was found for Ca at 4.531 µg/m3, followed by Na (3.905 µg/m3), Fe (2.464 µg/m3), Zn (2.311 µg/m3), K (2.086 µg/m3), Mg (0.962 µg/m3), Cu (0.306 µg/m3), Sb (0.157 µg/m3), Pb (0.144 µg/m3) and Sr (0.101 µg/m3). On an average basis, the decreasing metal concentration trend was: Ca > Na > Fe > Zn > K > Mg > Cu > Sb > Pb > Sr > Mn > Co > Ni > Cr > Li > Cd ≈ Ag. The TSP levels varied from a minimum of 41.8 to a maximum of 977 µg/m3, with a mean value of 164 µg/m3, which was found to be higher than WHO primary and secondary standards. The correlation study revealed very strong correlations (r?>?0.71) between Fe–Mn, Sb–Co, Na–K, Mn–Mg, Pb–Cd and Sb–Sr. Among the meteorological parameters, temperature, wind speed and pan evaporation were found to be positively correlated with TSP, Ca, Fe, K, Mg, Mn and Ag, whereas, they exhibited negative relationships with relative humidity. On the other hand, Pb, Sb, Zn, Co, Cd and Li revealed significant positive correlations with relative humidity and negative with temperature, wind speed and pan evaporation. The major sources of airborne trace metals identified with the help of principle component analysis and cluster analysis were industrial emissions, automobile exhaust, biomass burning, oil combustion, fugitive emissions, resuspended soil dust and earth crust. The TSP and selected metals were also studied for seasonal variations, which showed that Na, K, Zn, Cu, Pb, Sb, Sr, Co and Cd peaked during the winter and remained lowest during the summer, while Ca, Fe, Mg and Mn were recorded highest during the spring.  相似文献   

20.
为了解包头市铜厂周边地区土壤剖面中重金属污染状况,采用火焰原子吸收分光光度法和Tessier连续提取法,对土壤中6种重金属（Cu,Zn,Mn,Ni,Pb和Cd）的垂直分布特征、形态及潜在生物可利用性进行了分析。结果表明:研究区土壤剖面各层土壤中6种重金属含量均超过内蒙古土壤背景值,Cu,Pb和Cd为主要污染物。随采样深度的增加,Cu,Zn,Pb和Mn的含量呈现下降趋势,且由相关性系数可知重金属Cu,Zn和Pb可能有相同人为或自然污染源;土壤剖面中6种重金属均主要以残渣态存在,含量均在50%以上,对生物危害较小;潜在生物可利用性分析结果为:Cu（32.61%） > Mn（31.85%） > Ni（24.90%） > Zn（16.60%） > Cd（15.23%） > Pb（14.87%）,Cu和Mn的潜在生物可利用性较大,其次为Ni,Zn,Cd和Pb潜在生物可利用性较小。  相似文献   

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