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1.
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   

2.

Purpose

The concentration of human activities in urban systems generally leads to urban environmental contamination. Beijing is one of ancient and biggest cities on the world. However, information is limited on Beijing’s soil contamination, especially for roadside and campus soils. Thus, the aims of this study were to investigate the contents and chemical forms of toxic heavy metals Cd, Cr, Cu, Ni, Pb, and Zn in the road-surface dust, roadside soils, and school campus soils of Beijing. In addition, enrichment and spatial variation of these toxic heavy metals in the soils and dust were assessed.

Materials and methods

Topsoil samples were collected from the schools and roadside adjacent to main ring roads, and dust samples were collected from the surface of the main ring roads of Beijing. These samples were analyzed for total contents and chemical forms of Cd, Cr, Cu, Ni, Pb, Sc, Zn, Al, and Fe. Enrichment factors (EFs, relative to the background content) were calculated to evaluate the effect of human activities on the toxic heavy metals in soils.

Results and discussion

Heavy metal contents in the road dust ranged from 0.16 to 0.80, 52.2 to 180.7, 18.4 to 182.8, 11.9 to 47.4, 23.0 to 268.3, and 85.7 to 980.9 mg kg?1 for Cd, Cr, Cu, Ni, Pb, and Zn, respectively. In the roadside soil and school soil, Cd, Cr, Cu, Ni, Pb, and Zn contents ranged from 0.13 to 0.42, 46.1 to 82.4, 22.7 to 71.6, 20.7 to 29.2, 23.2 to 180.7, and 64.5 to 217.3 mg kg?1, respectively. The average EF values of these metals were significantly higher in the dust than in the soils. In addition, the average EF values of Cd, Cu, Pb, and Zn in the soils near second ring road were significantly higher than those near third, fourth, and fifth ring roads. Anthropogenic Cd, Pb, and Zn were mainly bound to the carbonates and soil organic matter, while anthropogenic Cu was mainly bound to oxides. The mobility and bioavailability of these metals in the urban soils of Beijing generally decreased in the following order: Cd?>?Zn?>?Pb?>?Cu?>?Ni?>?Cr; while in the dust, they decreased in the following order: Zn, Cu, and Cd?>?Pb?>?Ni?>?Cr.

Conclusions

Both EF and chemical forms documented that Cr and Ni in the soils and dust mainly originated from native sources, while Cd, Cu, Pb, and Zn partially originated from anthropogenic sources. In overall, Beijing’s road dust was significantly contaminated by Cd and Cu and moderately contaminated by Cr, Pb, and Zn, while Beijing’s roadside soil and school soil were moderately contaminated by Cd and Pb. However, the maximal hazard quotients (HQs) for individual Cd, Cr, Cu, Ni, Pb, and Zn and comprehensive hazard index (HI) of these metals in the dust and soil were less than 1, indicating that the heavy metals in the dust and soil generally do not pose potential health effects to children, sensitive population.  相似文献   

3.
Retention of Cd, Cu, Pb and Zn by Wood Ash, Lime and Fume Dust   总被引:2,自引:0,他引:2  
Heavy metals are of interest due to their deleterious impacts on both human and ecosystem health. This study investigated the effectiveness of wood ash in immobilizing the heavy metals Pb, Cd, Cu and Zn from aqueous solutions. The effects of initial metal concentrations, solution pH, ash dose and reaction time on metal sorption, as well as the metal sorption mechanisms were studied. To investigate the effect of initial metal concentrations, solutions containing Cd, Zn (25, 50, 75, 100 or 125 mg L?1), Cu (25, 50, 75, 100, 125, 150 or 175 mg L?1) or Pb (250, 500, 750, 1000, 1250, or 1500 mg L?1) were reacted with 10 g L?1 ash for two hours. For the effect of pH, solutions containing 100 mg L?1 of Cd, Cu or Zn or 1500 mg L?1 of Pb were reacted with 15 g L?1 ash over a pH range of 4 to 7. The wood ash was effective in immobilizing the four metals with a sorption range of 41–100 %. The amounts of metals retained by the ash followed the order of Pb > Cu > Cd > Zn. As expected, absolute metal retention increased with increasing initial metal concentrations, solution pH and ash dose. Metal retention by the ash exhibited a two-phase step: an initial rapid uptake of the metal followed by a period of relatively slow removal of metal from solution. Metal retention by the ash could be described by the Langmuir and Freundlich isotherms, with the latter providing a better fit for the data. Dissolution of calcite /gypsum minerals and precipitation of metal carbonate/sulfate like minerals were probably responsible for metal immobilization by the ash in addition to adsorption.  相似文献   

4.
Toxicity of heavy metals (Zn,Cu, Cd,Pb) to vascular plants   总被引:1,自引:0,他引:1  
The literature on heavy metal toxicity to vascular plants is reviewed. Special attention is given to forest plant species, especially trees, and effects at low metal concentrations, including growth, physiological, biochemical and cytological responses. Interactions between the metals in toxicity are considered and the role of mycorrhizal infection as well. Of the metals reviewed, Zn is the least toxic. Generally plant growth is affected at 1000 μg Zn L?1 or more in a nutrient solution, though 100 to 200 µg L?1 may give cytological disorders. At concentrations of 100 to 200 μg L?1, Cu and Cd disturb metabolic processes and growth, whereas the phytotoxicity of Pb generally is lower. Although a great variation between plant species, critical leaf tissue concentrations affecting growth in most species being 200 to 300 μg Zn g?1 dry weight, 15 to 20 μg Cu g?1 and 8–12 μg Cd g?1. With our present knowledge it is difficult to propose a limit for toxic concentrations of Zn, Cu, Cd and Pb in soils. Besides time of exposure, the degree of toxicity is influenced by biological availability of the metals and interactions with other metals in the soil, nutritional status, age and mycorrhizal infection of the plant.  相似文献   

5.
Trace metal concentrations were measured in the tissues of fish, molluscs, crustaceans and macrophytes from St. Vincent Gulf, South Australia. The concentrations of the measured metals (Cd < 0.025 to 2.1 μg g?1; Cu 0.51 to 9l μg g?1 5 Pb 0.02 to 3.6 ?g g?1; Zn l5 to 110 μg g?1)are similar to those from unpolluted areas and thus give no indication of pollution.  相似文献   

6.
The effects of cadmium and copper on larval metamorphosis and mortality of cultured Capitella sp Y were investigated. Metatrochophore larvae were exposed to 0.013 (control), 0.030, 0.080, 0.120, and 0.170 mg Cd L?1 and 0.017 (control), 0.025, 0.060, and 0.075 mg Cu L?1 for 34 days. Larval mortality significantly (p < 0.01) increased with increasing Cd and Cu concentrations (Kruskal-Wallis test), with similar effects for both metals for day 10 (LC50 = 0.035 mg Cd L?1 and 0.035 mg Cu L?1). Metamorphosis was inhibited in larvae exposed to the two metals in the absence of food, the effect of Cu being the most severe. This study suggests that Cd and Cu exposure could be harmful to early developmental stages of Capitella sp Y producing a delay in recruitment into natural populations.  相似文献   

7.
Samples of soils and vegetation from the mining area of South-West Sardinia (Italy) were analyzed for Pb, Zn, Cd, and Cu content. The area (more than 100 km2) is inhabited by many thousands of people; land utilization includes mainly grapes on some small plains and permanent sheep pasture on the hills. The levels of Pb, Zn, and Cd were found to be exceptionally high in most samples. Lead concentration was up to 71000 μg g?1 in the soils and 4000 jig g?1 in vegetation; Cd concentration was found up to 665 μg g?1 in soils and 26.5 μg g?1 in vegetation. The heavy metal content of some soil samples was highly variable. Data show that Pb is easily absorbed by plant roots and translocated to foliage. In spite of the high heavy metal level, no signs of toxicity were apparent in vegetation.  相似文献   

8.
Soil and water samples were analysed for trace metals and As in two watercourses and 14 sampling plots in a salt marsh polluted by mine wastes in SE Spain. Groundwater levels, soil pH and Eh were measured ‘in situ’ for a 12-month period in each sampling plot, and total calcium carbonate was also determined. Low concentrations of soluble metals (maximum Mn 1.089 mg L?1 and maximum Zn 0.553 mg L?1) were found in the watercourses. However, total metal contents were extremely high in the soils of a zone of the salt marsh (maximum 1,933 mg kg?1 of Mn, 62,280 mg kg?1 of Zn, 16,845 mg kg?1 of Pb, 77 mg kg?1 of Cd, 418 mg kg?1 of Cu and 725 mg kg?1 of As), and soluble metals in the pore water reached 38.7 mg L?1 for Zn, 3.15 mg L?1 for Pb, 48.0 mg L?1 for Mn, 0.61 mg L?1 for Cd and 0.29 mg L?1 for As. Variable concentrations with depth indicate a possible re-mobilisation of the metals, which could be related to spatial and temporal variations of water table level, pH and Eh and to the presence of calcium carbonate. A tendency for the Eh to decrease in the warmest months and to increase in the coldest ones was found, especially, in plots that received water with a high content of dissolved organic carbon. Hence, the existence of nutrient effluent-enriched water may modify the physical–chemical conditions of the soil–water system and influence metal mobility.  相似文献   

9.
Recovery of valuable metals from acidic mine drainage (AMD) during bioremediation using straw bioremediation system was investigated, with observation of efficient metal recovery. The recovery loading rates of Cu and Zn were 46.19?±?6.13 and 43.86?±?6.76?mg?m?3?h?1, respectively. More than 97.0% of Cu and more than 87.0% of Zn were recovered from AMD during bioremediation. The recovery loading rate of Cu increased by 4.54?mg?m?3?h?1 for each 1?mg?L?1 increase in influent concentration while that of Zn increased by 4.08?mg?m?3?h?1. Heavy metal toxic effect on the metal recovery in the straw bioremediation system could be neglected in most cases. Low pH could severely decrease recovery rate of Zn, while it had no influence on that of Cu. The recovery loading rate of Zn decreased by almost 70% when the influent pH decreased from 7.0 to 3.0. Cu could be recovered efficiently even at a short hydraulic residence time (HRT) of 18?h, while Zn could only be efficiently recovered at a relatively long HRT of 80?h, indicating that selective metal recovery might be achieved with relatively short HRT and bioreactor process optimization. These findings suggested the feasibility of using sulfate-reducing straw bioremediation system to recover valuable metals during bioremediation of AMD.  相似文献   

10.
Abstract

The accumulation of heavy metals in plants is related to concentrations andchemical fractions of the metals in soils. Understanding chemical fractions and availabilities of the metals in soils is necessary for management of the soils. In this study, the concentrations of copper (Cu), cadmium (Cd), lead (Pb), and zinc (Zn) in tea leaves were compared with the total and extractable contents of these heavy metals in 32 surface soil samples collected from different tea plantations in Zhejiang province, China. The five chemical fractions (exchangeable, carbonate‐bound, organic matter‐bound, oxides‐bound, and residual forms) of the metals in the soils were characterized. Five different extraction methods were also used to extract soil labile metals. Total heavy metal contents of the soils ranged from 17.0 to 84.0 mgCukg?1, 0.03 to 1.09 mg Cd kg?1, 3.43 to 31.2 mg Pb kg?1, and 31.0 to 132.0 mg Zn kg?1. The concentrations of exchangeable and carbonate‐bound fractions of the metals depended mainly on the pH, and those of organic matter‐bound, oxides‐bound, and residual forms of the metals were clearly controlled by their total concentrations in the soils. Extractable fractions may be preferable to total metal content as a predictor of bioconcentrations of the metals in both old and mature tea leaves. The metals in the tea leaves appeared to be mostly from the exchangeable fractions. The amount of available metals extracted by 0.01 mol L?1 CaCl2, NH4OAc, and DTPA‐TEA is appropriate extractants for the prediction of metals uptake into tea plants. The results indicate that long‐term plantation of tea can cause sol acidification and elevated concentrations of bioavailable heavy metals in the soil and, hence, aggravate the risk of heavy metals to tea plants.  相似文献   

11.
The effects of Hg, As, Pb, Cu, Cd, and Cr (1, 2, and 5 mg L?1 each) on Azolla pinnata R. Br. were analyzed. The treatments (2 and 5 mg L?1) of the heavy metal pollutants decreased Hill activity, chlorophyll, protein and dry wt, and increased tissue permeability over control values. The effects were most pronounced with the treatment of 5 mg L?1. The harmful effects of the metals were, in general, found by the treatments in the order: Cd 〉 Hg 〉 Cu 〉 As 〉 Pb 〉 Cr. There was no significant change in these parameters at 1 mg L?1 of the metals over control. Thus Azolla pinnata shows tolerance to the heavy metals tested up to 1 mg L?1 each.  相似文献   

12.
The concentrations of Hg, Cu, Pb, Cd, and Zn accumulated by regional macrophytes were investigated in three tropical wetlands in Colombia. The studied wetlands presented different degrees of metal contamination. Cu and Zn presented the highest concentrations in sediment. Metal accumulation by plants differed among species, sites, and tissues. Metals accumulated in macrophytes were mostly accumulated in root tissues, suggesting an exclusion strategy for metal tolerance. An exception was Hg, which was accumulated mainly in leaves. The ranges of mean metal concentrations were 0.035?C0.953 mg g?1 Hg, 6.5?C250.3 mg g?1 Cu, 0.059?C0.245 mg g?1 Pb, 0.004?C0.066 mg g?1 Cd, and 31.8?363.1 mg g?1 Zn in roots and 0.033?C0.888 mg g?1 Hg, 2.2?C70.7 mg g?1 Cu, 0.005?C0.086 mg g?1 Pb, 0.001?C0.03 mg g?1 Cd, and 12.6?C140.4 mg g?1 Zn in leaves. The scarce correlations registered between metal concentration in sediment and plant tissues indicate that metal concentrations in plants depend on several factors rather than on sediment concentration only. However, when Cu and Zn sediment concentrations increased, these metal concentrations in tissues also increased in Eichhornia crassipes, Ludwigia helminthorriza, and Polygonum punctatum. These species could be proposed as Cu and Zn phytoremediators. Even though macrophytes are important metal accumulators in wetlands, sediment is the main metal compartment due to the fact that its total mass is greater than the corresponding plant biomass in a given area.  相似文献   

13.
Abstract

Equilibrium adsorption experiments on zinc (Zn), cadmium (Cd), copper (Cu), and lead (Pb) were conducted in three horizons of two Ultisols and one Oxisol with and without liming, from Viçosa‐MG (Brazil). Equilibrium solutions were applied as a “cocktail”; containing 700 mg L‐1 of Zn, 20 mg L#lb1 of Cd, 200 mg L‐1of Cu, and 300 mg L‐1 of Pb and its dilutions of 1:5 and 1:20. After shaking, the mixture was centrifuged, the supernatant collected and the pH and the concentrations of metals in the mixture were determined. Soil order, soil horizon, and liming had significant effects on the metal adsorption. Some important changes in the adsorption characteristics of the metals, especially in Zn and Cd, were observed due to competition between the different cations present in the solution. Also, desorption of Zn and Cd was observed with an increasing concentration of the solution. The adsorption data for Zn and Cd did not fit the linear, Langmuir, Freundlich, and Temkin isotherm equations for most situations, as these equations do not consider the possibility of a decrease in the amount of metal adsorbed with increasing metal competition for the adsorption sites. Due to the competition with other metals, the equations, which offered the best fit for Zn and Cd, were quadratic polynomial models. On the other hand, for Cu and Pb, the equations, which showed the best fit were linear, Langmuir, and Temkin, for different situations. The reasons for this behavior were related to the strong competitive forces for the adsorption sites presented by these two metals.  相似文献   

14.
To help expand our global perspective on trace metal contamination, concentrations of Cu, Fe, Hg, Mn, Ni, Pb, and Zn were determined for sediments from the Ebrie Lagoon in the Ivory Coast, a developing West African nation. Excess loading of several metals, especially Hg, Pb, and Zn was found at several sites. The maximum concentration of Hg measured in sediments from the Ebrie Lagoon (2250 ng g?1) is about 30 times greater than natural levels. Similarly, Pb and Zn concentrations for the Ivorian lagoonal sediments are as high as 250 and 560 μg g?1, respectively, showing sizeable anthropogenic inputs. Trace metal sources to the Ebrie Lagoon include untreated sewage and industrial wastes.  相似文献   

15.
The Algal Assay Procedure Bottle Test was used to investigate the effect of Cd, Cu, and Cr (VI) on the growth of Nile water algae. The results of this investigation indicated that Cd has slight inhibitory effects on algal growth at low concentration (0.05 mg L?1), while it was inhibiting algal growth at higher concentration (> 1.0 mg L?1). In contrast, Cu and Cr did not affect algal growth in all investigated concentrations. Combinations of Cd with Cu and Cr seemed to interact synergistically. The synergism between Cd and Cu was more pronounced than between Cd and Cr. Clear changes in the diversity and redundancy of algal structure took place after metal addition. The inhibitory effect of the studied metals was in the following order: Cd-Cu > Cd - Cr > Cd > Cu > Cr.  相似文献   

16.
Changes in the soil chemical environment can be expected to increase the leaching of trace metals bound in soils. In this study the mobility of trace metals was monitored in a column experiment for two contaminated urban soils. Four different treatments were used (i.e. rain, acid rain, salt and bark). Leachates were analysed for pH, dissolved organic carbon (DOC) and for seven trace metals (cadmium (Cd), chromium (Cr), copper (Cu), mercury (Hg), nickel (Ni), lead (Pb) and zinc (Zn)). The salt treatment produced the lowest pH values (between 5 and 6) in the effluent whereas the DOC concentration was largest in the bark treatment (40–140 mg L?1) and smallest in the salt and acid treatments (7–40 mg L?1). Cadmium, Ni and Zn were mainly mobilised in the salt treatment, whereas the bark treatments produced the highest concentrations of Cu and Pb. The concentrations of Cu, Cr, and Hg were strongly correlated with DOC (r 2?=?0.90, 0.91 and 0.96, respectively). A multi-surface geochemical model (SHM-DLM) produced values for metal dissolution that were usually of the correct magnitude. For Pb, however, the model was not successful indicating that the retention of this metal was stronger than assumed in the model. For all metals, the SHM-DLM model predicted that soil organic matter was the most important sorbent, although for Pb and Cr(III) ferrihydrite was also important and accounted for between 15 and 50% of the binding. The results confirm the central role of DOC for the mobilization of Cu, Cr, Hg and Pb in contaminated soils.  相似文献   

17.

Purpose

Heavy metal distribution in soils is affected by soil aggregate fractionation. This study aimed to demons trate the aggregate-associated heavy metal concentrations and fractionations in “sandy,” “normal,” and “mud” soils from the restored brackish tidal marsh, oil exploitation zone, and tidal mudflat of the Yellow River Delta (YRD), China.

Materials and methods

Soil samples were sieved into the aggregates of >2, 0.25–2, 0.053–0.25, and <0.053 mm to determine the concentrations of exchangeable (F1), carbonate-bound (F2), reducible (F3), organic-bound (F4), and residual fraction (F5) of Cd, Cr, Cu, Ni, Pb, and Zn.

Results and discussion

The 0.25–2 mm aggregates presented the highest concentrations but the lowest mass loadings (4.23–12.18 %) for most metal fractions due to low percentages of 0.25–2 mm aggregates (1.85–3.12 %) in soils. Aggregates <0.053 mm took majority mass loadings of metals in sandy and normal soils (62.04–86.95 %). Most soil aggregates had residual Cr, Cu, Ni, Zn, and reducible Cd, Pb dominated in the total Cd, Cr, Cu, Ni, Pb, and Zn concentrations. Sandy soil contained relatively high F4, especially of Cu (F4) in 0.25–2 mm aggregates (10.22 mg kg?1), which may relate to significantly high organic carbon contents (23.92 g kg?1, P?<?0.05). Normal soil had the highest total concentrations of metals, especially of Cu, Ni, and Pb, which was attributed to the high F3 and F5 in the <0.053 mm aggregates. Although mud soil showed low total concentrations of heavy metals, the relatively high concentrations of bioavailable Cd and Cu resulted from the relatively high Cd (F2) and Cu (F2) in the >2 mm aggregates indicated contribution of carbonates to soil aggregation and metal adsorption in tidal mud flat.

Conclusions

Soil type and aggregate distribution were important factors controlling heavy metal concentration and fractionation in YRD wetland soil. Compared with mud soil, normal soil contained increased concentrations of F5 and F3 of metals in the 0.053–0.25 mm aggregate, and sandy soil contained increased concentrations of bioavailable and total Cr, Ni, and Zn with great contribution of mass loadings in the <0.053 mm aggregate. The results of this study suggested that oil exploitation and wetland restoration activities may influence the retention characteristics of heavy metals in tidal soils through variation of soil type and aggregate fractions.
  相似文献   

18.

Purpose

The objectives of this study were to explore the influences of pH on the release of Cu, Zn, Cd, Pb, Ni, and Cr in sediments derived from the upstream, middle, and downstream reaches of Dongdagou stream in Gansu Province, Northwest China, and to examine the fractionation changes of heavy metals in the sediments after reaching their release equilibrium under different pH conditions.

Materials and methods

Sediment samples were obtained using a stainless steel grab sampler to collect the uppermost 10 cm of sediment from the channel bed. The pH-dependent release experiment was conducted in the solid-to-liquid ratio of 1:20 at different pH values (2, 4, 6, 8, 10, and 12) at room temperature. The total Cu, Zn, Cd, Pb, Ni, and Cr concentrations in the sediments were digested using an acid digestion mixture (HNO3 + HF + HClO4) in an open system. Metal fractionation of selected sediments was obtained using the Tessier sequential extraction procedure. Heavy metal concentrations in the samples were determined using atomic absorption spectrophotometry.

Results and discussion

The mean concentrations of heavy metals in sediments decreased in the following order: Zn (1676.67 mg kg?1) > Pb (528.65 mg kg?1) > Cu (391.34 mg kg?1) > Cr (53.48 mg kg?1) > Ni (34.27 mg kg?1) > Cd (11.53 mg kg?1). Overall, the solubility of Cu, Zn, Cd, Pb, and Ni decreased with increasing pH, and they were strongly released at pH 2. Moreover, the solubility of Cr increased with increasing pH, and its release was highest at pH 12. After reaching the release equilibrium of heavy metals under different pH conditions, the percentages of organic Cu, Zn, Cd, and Fe-Mn oxyhydroxide Pb decreased, compared to their initial fractions. The residual fractions of Ni and Cr were dominant, regardless of pH.

Conclusions

The average concentrations of Cu, Zn, Cd, and Pb in sediments were highly elevated compared with the soil background values in Gansu Province, China. The results of this pH-dependent release experiment showed that the release behaviors of Cu, Zn, Pb, and Cr followed an asymmetric V-shaped pattern, whereas Cd and Ni followed an irregular L-shaped pattern. The changes in the release of heavy metals in sediments were related to their redistribution between chemical fractionations.
  相似文献   

19.
The bioavailability and plant uptake of heavy metals (HM), as well as finding the most reliable methods for the prediction of availability, continues to be one of the most crucial problems in agricultural and environmental studies. In agricultural soils from two regions in Kosovo, known for its metal pollution, we collected 60 soil and plant samples (wheat, corn, potatoes, and grass). Heavy metals were extracted from soil with aqua regia (pseudototal concentration), NH4OAc‐EDTA (potential bioavailable), and NH4NO3 (mobile fraction), plant samples were digested with HNO3/H2O2 (microwave assisted extraction). The pseudo total content of Cd, Pb, and Zn showed high value in Mitrovice (mean: Cd–2.92, Pb–570.15, and Zn–522.86 mg kg?1), whereas in Drenas region Ni and Cr showed high value with a mean 258.54 and 203.22 mg kg?1. Also, the potential bioavailability and mobile form of these metals were increased in Mitrovice (mean: Cd–1.59, Pb–217.05, Zn–522.86 mg kg?1, respectively Cd–0.17, Pb–0.64, and Zn–15.45 mg kg?1), compared to Drenas. Cd and Pb were elevated in potato tubers (mean Cd–0.48 and Pb–0.85 mg kg?1). The TF was higher for micronutrients (Zn and Cu) than for non‐essential metals (Cd and Pb). Multiple regression analysis showed a good model for prediction of Cd, Pb and Zn content in plant with significance 99.9%, whereas this model was not significant for Cu, Cr, and Ni. Soil pH played a significant role in the content of Cd and Zn in wheat and potato plants. Clay content also showed significance in Cd concentration in wheat and potato plants, while carbon content was significant for Cd in grass plants, as well as for Zn in wheat and grass plants.  相似文献   

20.
Barley (Hordeum vulgare L.) was grown on a sandy soil given different doses of cadmium carbonate (salt), copper carbonate (malachite), lead carbonate (cerussite), and zinc carbonate (smithsonite) in a pot experiment conducted in a greenhouse. The element compounds were added to the soil in amounts equivalent to the following levels of the metals: Cd 5, 10, 50 μq ?1; Cu and Pb 50, 100, 500 μg g?1; Zn 150, 300, 1500 μg g?1. Sequential extraction was used for partition these metals into five operationally-defined fractions: exchangeable, bound to carbonates, bound to Fe-Mn oxides, bound to organic matter and residual. The residue was the most abundant fraction in the untreated soil for all the metals studied (43 to 61% of the total contents). The concentration of exchangeable Cd (0.2 μg g?1), Cu (0.01 μg g?1), Pb (0.1 μg g?1), and Zn (1.4 μg g?1) were relatively low in the untreated soil but increased markedly in the treated soils for Cd (up to 31 μg g?1) and Zn (up to 83 μg g?1), whereas only small changes were observed for Cu and Pb. The pot experiment showed a significant increase in the Cd and Zn contents of barley grown on the treated soils, but only small changes in Cu and Pb concentrations.  相似文献   

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