Contents and chemical forms of heavy metals in school and roadside topsoils and road-surface dust of Beijing

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.     

The transfer of heavy metals to barley plants from soils amended with sewage sludge with different heavy metal burdens

Purpose

Our main aim objective was to evaluate the transfer of Cd, Cr, Cu, Ni, Pb and Zn to barley (Hordeum vulgare) grown in various soils previously amended with two sewage sludges containing different concentrations of heavy metals. This allowed us to examine the transfer of heavv metals to barley roots and shoots and the occurrence of restriction mechanisms as function of soil type and for different heavy metal concentration scenarios.

Material and methods

A greenhouse experiment was performed to evaluate the transfer of heavy metals to barley grown in 36 agricultural soils from different parts of Spain previously amended with a single dose (equivalent to 50 t dry weight ha^?1) of two sewage sludges with contrasting levels of heavy metals (common and spiked sludge: CS and SS).

Results and discussion

In soils amended with CS, heavy metals were transferred to roots in the order (mean values of the bio-concentration ratio in roots, BCF_Roots, in brackets): Cu (2.4)?~?Ni (2.3)?>?Cd (2.1)?>?Zn (1.8)?>?Cr (0.7)?~?Pb (0.6); similar values were found for the soils amended with SS. The mean values of the soil-to-shoot ratio were: Cd (0.44)?~?Zn (0.39)?~?Cu (0.39)?>?Cr (0.20)?>?Ni (0.09)?>?Pb (0.01) for CS-amended soils; Zn (0.24)?>?Cu (0.15)?~?Cd (0.14)?>?Ni (0.05)?~?Cr (0.03)?>?Pb (0.006) for SS-amended soils. Heavy metals were transferred from roots to shoots in the following order (mean values of the ratio concentration of heavy metals in shoots to roots in brackets): Cr (0.33)?>?Zn (0.24)?~?Cd (0.22)?>?Cu (0.19)?>?Ni (0.04)?>?Pb (0.02) for CS-amended soils; Zn (0.14)?>?Cd (0.09)?~?Cu (0.08)?>?Cr (0.05)?>?Ni (0.02)?~?Pb (0.010) for SS-amended soils.

Conclusions

Soils weakly restricted the mobility of heavy metals to roots, plant physiology restricted the transfer of heavy metals from roots to shoots, observing further restriction at high heavy metal loadings, and the transfer of Cd, Cu and Zn from soils to shoots was greater than for Cr, Ni and Pb. Stepwise multiple linear regressions revealed that soils with high sand content allowed greater soil-plant transfer of Cr, Cu, Pb and Zn. For Cd and Ni, soils with low pH and soil organic C, respectively, posed the highest risk.     

Evaluation and source identification of trace element contamination of soils in the Qixia lead-zinc mining area,Jiangsu, China

Purpose

The Qixia mine is one of the largest lead-zinc mines in Eastern China and has been operational for approximately 60 years. Source identification for trace element contamination of soils in the Qixia mining area has been lacking. This report details the evaluation and source identification of trace element contamination (including Cu, Zn, Pb, Cd, Hg, Cr, As, and Ni) of soils in this area.

Materials and methods

Thirty-three soil samples from roadsides and fields in the study area were collected and analyzed. The index of geo-accumulation (I _geo) was employed to evaluate contamination. Methods of multivariate statistical analysis were used to determine the probable sources of the pollutants.

Results and discussion

The analysis showed that the levels of contamination ranked in the following order: Cd > Pb/Zn> > As/Cu> > Hg > Cr/Ni. In the sampling area nearest the mine, soil samples collected from roadsides showed much higher levels of contamination than those collected from fields away from the roadways. Trace element contamination decreased as the distance from the mine increased. Contamination extended to a distance of approximately 700 m from mineral transportation routes, with the area of greatest impact at 200 m or less. Multivariate statistical analysis and ore composition data suggest that the Cu, Zn, Pb, Cd, and As found in the soil samples originate from anthropogenic sources. Ni and Cr are considered to be at natural background concentrations.

Conclusions

This study distinguished between natural and anthropogenic sources of trace element contamination in the soils of the Qixia mining area. The contamination of Cu, Zn, Pb, Cd, and As is linked to the mining activities and is likely due to the transportation of ore concentrates and tailings.     

Trace metals in sediments and aquatic plants from the Xiangjiang River, China

Purpose

The metal concentrations and Pb isotopic composition in sediments and plants from the Xiangjiang River, China, were investigated to understand the contamination and potential toxicity of metals in sediments; to determine the accumulation and distribution of metals in plant tissues; and to trace the possible pollution source of Pb in sediments and plants.

Materials and methods

Sediments and plants were collected from 43 sampling sites in the study region. After sediments were air-dried and passed through a 63-??m sieve, they were acid-digested and DTPA-extracted for determination of total and bioavailable metals. The plants were separated into roots, leaves, and stems; dried; cut into pieces; and digested with HNO₃?CH₂O₂. Metals (As, Cd, Cr, Cu, Ni, Pb, and Zn) and Pb isotopic composition were analyzed by inductively coupled plasma-mass spectrometry.

Results and discussion

Maximum As, Cd, Cr, Cu, Ni, Pb, and Zn concentrations in sediments were 47.18, 55.81, 129.5, 161.6, 160.4, 430.7, and 1,098.8?mg?kg^?1, respectively. The bioavailable fractions of As, Cd, Cu, Pb, and Zn had significant linear relationship with their corresponding total contents in sediments while no significant relationship was observed between bioavailable and total contents of Cr and Ni. In general, plant tissues showed higher As, Cd, Cu, Pb, and Zn concentrations and lower Cr and Ni concentrations compared with sediments. The ²⁰⁶Pb/²⁰⁷Pb ratios decreased in the order of total > bioavailable > stems ?? leaves > roots. A strong linear correlation was observed between the ²⁰⁸Pb/²⁰⁶Pb and ²⁰⁶Pb/²⁰⁷Pb ratios of the plant tissues, sediments, and the possible pollution sources of Pb in the Xiangjiang River.

Conclusions

As, Cd, Cu, Pb, and Zn demonstrated higher contamination levels in sediments and plants compared with Cr and Ni. Cd had highest potential ecological risk. The Pb from anthropogenic sources with low ²⁰⁶Pb/²⁰⁷Pb ratios was preferentially associated with the bioavailable fractions in sediments and accumulated in roots. The Pb in plant tissues is mainly derived from the Pb in sediment and is taken up through the sediment-to-root pathway.     

Mixed chelators of EDTA,GLDA, and citric acid as washing agent effectively remove Cd,Zn, Pb,and Cu from soils

Purpose

Soil washing with chelators is a viable treatment alternative for remediating multi-contaminated soils. The aim of this study was to investigate the removal efficiencies of Cd, Zn, Pb, and Cu in alkaline and acid multi-metal-contaminated soils by washing with the mixed chelators (MC).

Materials and methods

The batch experiments were carried out to evaluate the removal efficiencies of heavy metals in contaminated soils by the MC with different molar ratios of EDTA, GLDA, and citric acid, and evaluated the washing factors, including contact time, pH, MC concentration, and single and multiple washings at the same MC dose, on the removal efficiencies.

Results and discussion

Results showed that the removal efficiencies for Cd, Zn, Pb, and Cu by the MC (the molar ratio of EDTA, GLDA, and citric acid was 1:1:3) were as much as those of the only EDTA washing from both soil at the same application dose of total chelators; moreover, the application dose of EDTA decreased by 80%. For the alkaline-contaminated soil, the removal efficiencies of Cd, Zn, Pb, and Cu decreased with the increasing of the solution pH, which was opposite to acid-contaminated soil. This was attributed to that the metal-ligand complex could be obviously re-adsorbed on the soil surface sites, particularly in low pH values. The removal efficiencies of Cd, Zn, Pb, and Cu depended on MC concentration. A higher MC concentration led to a more effective removal of Cd, Zn, Pb, and Cu in alkaline-contaminated soil; however, their changes were slightly increased in acid-contaminated soil. At the same dose of MC, single washing with higher MC concentration might be favorable to remove heavy metals, moreover, with much less wastewater generation.

Conclusions

The MC (the molar ratio of EDTA, GLDA, and citric acid was 1:1:3) may be a useful, environmentally friendly, and cost-effective chelators to remediate heavily multi-metal-contaminated soil.

     

Spatial distribution and source apportionment of the heavy metals in the agricultural soil in a regional scale

Purpose

Understanding the spatial distribution and sources of soil heavy metals (HMs) in a large city helps prevent and control soil pollution. This study aimed to investigate the spatial patterns of soil HMs and identify their main sources in a regional scale.

Materials and methods

A total of 110 topsoil samples were collected from Tai’an City, China. Cd, Cr, Cu, Hg, Ni, Pb, and Zn concentrations in each soil sample were determined. Geostatistics, geographic information system (GIS), and positive matrix factorization (PMF) were used to explore the spatial distribution of seven soil HMs and to reveal the main sources of soil HMs in Tai’an City, respectively.

Results and discussion

Soil Cd, Cr, Pb, and Zn generally showed slight pollution levels in the study area. However, soil Hg and Cu contents reached moderate to heavy pollution levels in some areas. Soil Hg content increased from north to south across the city, and the highest Hg concentration was detected in Ningyang County. Soil Cd, Cu, and Zn distributions exhibited a similar pattern, and their contents increased from west to east; the highest Cd, Cu, and Zn concentrations were found in Xintai County. The highest soil Ni concentration was obtained in the northeast of Feicheng and Xintai counties. PMF analysis revealed the following four potential sources of agricultural soil HMs in Tai’an City: industrial and mining activities, agricultural activities, residential living activities, and business activities. Soil Hg mainly originated from residential living activities, which accounted for 75.3% of the total source. The main sources of soil Ni were residential living activities, agricultural activities, and industrial and mining activities, which account for 38.2, 27.50, and 25.1% of the total source, respectively. Soil Cu was mainly produced by agricultural activities (36.6%), followed by residential living activities (29.8%) and industrial and mining activities (25.8%).

Conclusions

PMF combined with GIS could be effectively applied to determine the main sources of HMs in agricultural soils in a regional scale.

     

Inorganic and organic pollution in agricultural soil from an emerging e-waste recycling town in Taizhou area, China

Purpose

The emerging recycling of electronic and electric waste (e-waste) is causing critical levels of soil pollution in those relatively poor towns surrounding the central cities, which have been involved in recycling activities for quite some time. Agricultural soil is of great importance due to its direct impact on food and human health. The objective of this study was to provide a systematic investigation of the contamination in agricultural soil for a range of inorganic compounds (Cr, Cd, Pb, Zn, Cu, and Ni) and organic compounds (PAHs and PCBs) in town A, an emerging e-waste recycling town in China.

Materials and methods

A total of 20 agricultural soil samples were collected from three sampling locations throughout town A. Levels of inorganic compounds (Cr, Cd, Pb, Zn, Cu, and Ni) and organic compounds (PAHs and PCBs) were determined by AAS, GC/MS, and GC/electron capture detector, respectively. Data was processed with SPSS 13 and Arcview 3.3 GIS software.

Results and discussion

The findings demonstrate that agricultural soil was contaminated to various extents by inorganic and/or organic pollutants. Comparison among the three sampling areas indicated that the soil was highly contaminated in the agricultural area near e-waste recycling workshops. Moreover, the contaminants (Cu, Pb, PAHs, and PCBs) may be connected through a common source as found in the Pearson correlations and cluster analysis.

Conclusions

There exists a heightened sense of awareness concerning the hazardous implications of current emerging e-waste recycling issues in the agricultural soil of those areas close to the central city in Taizhou.     

Heavy metal distribution in different soil aggregate size classes from restored brackish marsh,oil exploitation zone,and tidal mud flat of the Yellow River Delta

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.

     

Defining soil geochemical baselines at small scales using geochemical common factors and soil organic matter as normalizers

Purpose

The establishment of geochemical baselines is essential for accurate evaluation of the present state of surface environments. In this study, normalization procedures (NP), which can improve the explanation of the natural variation of elements, were conducted using geochemical common factors (GCF) and soil organic matter (SOM) as normalizers to define the geochemical baselines of soil trace elements.

Materials and methods

Soil samples (n?=?345) were collected in Luhe County, Jiangsu, China, a county with a complex geologic setting and intensive anthropogenic influence. Conservative elements, Al, Ca, Fe, K, Mg, Mn, Na, P, and Ti; trace elements, As, Cd, Cr, Cu, Hg, Ni, Pb, and Zn; and SOM were measured. Normalization procedures were conducted using multiple linear regressions between soil trace elements and SOM and GCFs, acquired from factor analysis of the soil major elements. Normalization procedures using univariate linear regressions between soil trace elements and conservative elements Al, Fe, and Ti were also conducted for comparison.

Results and discussion

Comparison of NPs using GCFs and SOM as normalizers with NPs, which use single conservative elements as normalizers, shows that the former is more accurate than the latter for As, Pb, and Zn and is as accurate for Cd, Cr, Cu, Hg, and Ni, when the most appropriate single conservative element is chosen. Small-scale geochemical baselines in the county are significantly different from regional-scale geochemical baselines for Jiangsu Province, China.

Conclusions

The application of regional-scale geochemical baselines at small scales may lead to estimation errors in determining anomalies and assessing environments. Baselines obtained from the NPs using GCFs and SOM as normalizers are more accurate.     

Heavy‐Metal Contamination of Soil and Vegetables in Wastewater‐Irrigated Agricultural Soil in a Suburban Area of Hanoi,Vietnam

The To Lich and Kim Nguu Rivers, laden with untreated waste from industrial sources, serve as sources of water for irrigating vegetable farms. The purposes of this study were to identify the impact of wastewater irrigation on the level of heavy metals in the soils and vegetables and to predict their potential mobility and bioavailability. Soil samples were collected from different distances from the canal. The average concentrations of the heavy metals in the soil were in the order zinc (Zn; 204 mg kg^?1) > copper (Cu; 196 mg kg^?1) > chromium (Cr; 175 mg kg^?1) > lead (Pb; 131 mg kg^?1) > nickel (Ni; 60 mg kg^?1) > cadmium (Cd; 4 mg kg^?1). The concentrations of all heavy metals in the study site were much greater than the background level in that area and exceeded the permissible levels of the Vietnamese standards for Cd, Cu, and Pb. The concentrations of Zn, Ni, and Pb in the surface soil decreased with distance from the canal. The results of selective sequential extraction indicated that dominant fractions were oxide, organic, and residual for Ni, Pb, and Zn; organic and oxide for Cr; oxide for Cd; and organic for Cu. Leaching tests for water and acid indicated that the ratio of leached metal concentration to total metal concentration in the soil decreased in the order of Cd > Ni > Cr > Pb > Cu > Zn and in the order of Cd > Ni > Cr > Zn > Cu > Pb for the ethylenediaminetetraaceitc acid (EDTA) treatment. The EDTA treatment gave greater leachability than other treatments for most metal types. By leaching with water and acid, all heavy metals were fully released from the exchangeable fraction, and some heavy metals were fully released from carbonate and oxide fractions. The concentrations of Cd, Cr, Cu, Ni, Pb, and Zn in the vegetables exceeded the Vietnamese standards. The transfer coefficients for the metals were in the order of Zn > Ni > Cu > Cd = Cr > Pb.     

Platinum-group and other traffic-related heavy metal contamination in road sediment, Guangzhou, China

Purpose

Human exposure to particulate matter emitted from on-road motor vehicles includes complex mixtures of heavy metals from tyres, brakes, part wear, and resuspended road sediment. The purpose of this study was to determine the concentrations of 14 platinum-group and other traffic-related heavy metals in road sediment within the metropolitan area of Guangzhou, China, with a view to identifying their sources and assessing the extent of anthropogenic influence on heavy metal contamination of road sediment.

Materials and methods

Thirty-five samples of road sediment were collected. The concentrations of Cr, Mn, Ni, Cu, Zn, La, Ce, Mo, Cd, Pb, Ba, and Rh were measured by inductively coupled plasma?Cmass spectrometry. Pt and Pd were analyzed by isotopic dilution?Cinductively coupled plasma?Cmass spectrometry. Multivariate statistical analysis and enrichment factor methods were employed to identify the sources of these heavy metals and to assess anthropogenic influences on their occurrence.

Results and discussion

The mean concentrations of Pt, Pd, Rh, Cr, Mn, Ni, Cu, Zn, La, Ce, Mo, Cd, Pb, and Ba in the road sediment samples were 68.24, 93.15, 23.85, 147.5, 712.3, 47.24, 177.5, 1254, 47.50, 96.62, 4.91, 3.00, 198.1, and 641.3?ng?g^?1, respectively. Very weak to significant linear positive correlations were found among the various heavy metals. The elemental composition of road sediment was dominated by five principal components. Three clusters were identified through cluster analysis, and enrichment factors were calculated relative to soils in China. The sources and degree of contamination of the heavy metals are discussed based on the results.

Conclusions

The mean concentrations of heavy metals are higher than background values, especially for Pt, Pd, Rh, Cd, and Zn. Four main sources are identified: (1) Pt, Pd, and Rh were derived from traffic sources; (2) La, Ce, Mn, and Ba were derived mainly from natural sources; (3) Cr, Ni, Cu, Mo, Cd, and Pb showed mixed traffic-industry sources; and (4) Zn originated mainly from industrial sources. Enrichment factor analysis supported this source identification and further indicated that contamination of road sediment in Guangzhou is extremely high for Pt, Pd, and Rh; moderate to very high for Cd, Zn, Pb, Cu, and Mo; and minimal for Cr, Ni, La, Ce, and Ba.     

Transfer of Cd, Pb, and Zn to water spinach from a polluted soil amended with lime and organic materials

Purpose

The transfer of heavy metals from soil to crops comprises several steps, including soil-to-root and subsequent root-to-shoot tranfer. The purpose of this study was to investigate the different steps of soil-to-crop transfer of Cd, Pb, and Zn.

Materials and methods

This study was carried out with a greenhouse pot experiment using a soil polluted with Cd, Pb, and Zn which was amended with rice straw, pig manure, sheep dung, or peat, with and without lime. Water spinach (Ipomoea aquatica) was used as the test crop and was grown after a season of rice cultivation.

Results and discussion

The results showed that all the amendments promoted the root-to-shoot transfer of Cd, Pb, and Zn. The soil-to-root transfer factors (TFs) of Pb and Zn tended to increase with increasing available Pb and Zn in the soils, while no clear relationship between the TF of Cd and available soil Cd was observed. The root-to-shoot TF of Cd, Pb, and Zn tended to decrease with increasing available amounts in the soils and were negatively correlated with the concentrations of the metals in the roots (r _Cd?=?0.820, r _Pb?=?0.789, r _Zn?=?0.769).

Conclusions

The soil-to-root transfer of Cd, Pb, and Zn was significantly different from the root-to-shoot transfer. The soil-to-root transfer was mainly influenced by the amount of available metal in soil, whereas the root-to-shoot transfer was mainly controlled by the concentrations of the metals in the root.     

污灌区土壤重金属空间结构与分布特征

该文探讨了地统计学插值模型应用于土壤重金属污染评价的适用条件,分析了北野场污灌区土壤重金属的正态分布特征和主导分布趋势,提出了不同重金属因子适宜的地统计插值模型。结果表明:土壤重金属空间变异系数处于12%～37%之间,整体变异性不大;Pb、Cd等因子的块金效应分别为0.90、0.87,空间相关性较弱,受人为随机因素的影响较大,As、Cr、Zn、Cu值等因子的块金效应分别为0.52、0.51、0.51和0.46,空间相关性中等,受人为随机因素和空间结构因素的共同作用,Hg和Ni的块金效应分别为0.253和0.06,空间相关性较强,受空间结构性因素的影响较大,可能受原生地质的影响较大。污灌区重金属含量存在增加趋势,灌区土壤重金属含量自北向南总体呈现较少趋势,这与灌区上下游灌溉保证率不同有关,表明长期污水灌溉可导致土壤重金属富集,但与全国其他污灌区相比,北野场污灌区土壤重金属污染相对较轻,应加强污水处理利用避免土壤重金属污染。     

Accumulation and potential sources of heavy metals in soils of the Hetao area, Inner Mongolia, China

Soil contamination by heavy metals is a problem in agricultural irrigation systems.To assess the accumulation and sources of heavy metals in the Yongji irrigation district of the Hetao area,Inner Mongolia,China,195 soil samples from 39 sites(0–100 cm)were collected,and Zn,Cu,Pb,Cr,and Cd concentrations were analyzed.The mean concentrations were 107.17,32.48,12.31,53.53,and 0.22 mg kg-1,respectively,with no significant differences between soil depths(P>0.05).Concentrations of Zn,Cu,and Cd were higher than the background levels,with moderate accumulation;the contamination factor(CF)values were 1.9,1.7,and 1.9,respectively,and the geoaccumulation index(Igeo)was>0.Concentrations of Pb and Cr were lower than,or close to,the background levels(CF<1,Igeo<0),indicating that they originated from a natural source.The monomial potential ecological risk index(Eri)for Zn,Cu,Pb,and Cr was low;Eri for Cd was 55.73,implying a moderate risk.The grade of potential ecological risk index of the five heavy metals(RI)was low,declining from south to north.The studied soils were contaminated with Zn,Cu,and Cd;principal component(PC)analysis implicated the enrichment of Cd and partial Cu(high loading in PC 2)was related to agricultural activities;Zn and partial Cu,closely associated with PC 3,may have originated from irrigation water from the Yellow River.Future agricultural development should focus on fertilizer and pesticide application and the quality of irrigation water.     

Long-term cultivation impact on the heavy metal behavior in a reclaimed wetland,Northeast China

Purpose

Heavy metal fractionation varies according to land uses. To understand the behavior of heavy metals in wetland soils under long-term agricultural cultivation, we examined the distribution, source, and associated environmental risk of heavy metals in different types of wetland soils.

Materials and methods

Soils were collected in cultivated lands, artificial ditches, and riparian zones from a reclaimed wetland in the Sanjiang Plain, Northeast China. They were analyzed for total concentrations and chemical fractions of Pb, Cd, Cu, Zn, Cr, and Ni, as well as pH, soil organic matter, total phosphorus, and particle size distribution.

Results and discussion

Heavy metal concentrations were significantly lower in cultivated wetland than in ditch and riparian wetlands. Riparian wetland was found to exhibit the highest metal concentrations. When compared with other two wetland types, the cultivated wetland showed much higher partitioning levels of heavy metals in the acid-soluble fraction and lower partitioning levels in the oxidizable fraction. Although Cr, Cu, and Ni in ditch and riparian wetlands were identified as the metal pollutants of primary concern, they had a low or no risk of further dispersion to other environmental components. Weathering of parent materials was the main source of Cr and Cu, Pb, Cd, and Zn originated mainly from agricultural practices, and Ni emanated from a mixture of sources.

Conclusions

Long-term agricultural cultivation can lead to significant heavy metal loss in cultivated wetland but enrich heavy metal concentrations in ditch and riparian wetlands. Periodic ditch dredging is considered an effective measure for decreasing heavy metal input into the fluvial system and thereby reducing the dispersion to the regional water environment.     

长期污灌农田土壤重金属污染及潜在环境风险评价

以西安市某典型污灌区农田土壤为研究对象,分析长期污水灌溉对表层土壤重金属含量及富集状况的影响,采用内梅罗指数法和Hakanson潜在生态危害指数法对其污染现状及潜在环境风险进行评价。结果表明：长期污灌已导致农田土壤Cd、Cr、Cu、Hg、Ni、Pb和Zn7种重金属相对自然背景有不同程度累积,其富集比例依次为100%、82.69%、100%、100%、80.77%、98.08%和100%,仅有土壤As平均含量低于其背景水平;以国家土壤环境质量标准二级限量值作为污染评价阈值,其中Cd和Hg污染表现突出,按其污染指数平均值排序为Cd〉Hg〉Ni〉Cu〉Zn〉As〉Cr〉Pb;土壤重金属综合潜在环境风险为＂强＂等级,Hg、Cd的环境影响占据主导;随污灌年限增长,离灌渠越近,农田土壤重金属的污染水平和环境风险越高。鉴于该区土壤重金属已呈现较强生态危害性,应及时采取必要防治措施,调整土地利用结构,确保农田环境及农产品安全生产。     

Assessment of diffuse pollution associated with metals in urban sediments using the geoaccumulation index (Igeo)

Purpose

This study investigated the behavior of cadmium (Cd), lead (Pb), nickel (Ni), and zinc (Zn) in urban sediments collected in commercial, residential, and industrial areas of the city of Porto Alegre, Brazil, and evaluated different degrees of pollution in this urban subdrainage basin through the use of the geoaccumulation index (I_geo).

Materials and methods

Concentrations of Cd, Ni, Pb, and Zn were analyzed using acid digestion (EPA method 3050) in fractions <63 μm in 20 composite samples of urban sediment collected using a portable vacuum in 20 different sampling points on roads from three areas with diverse use: commercial, industrial, and residential.

Results and discussion

The values of I_geo were commercial area (3.35, Zn; 3.76, Cd; 3.60, Ni; 2.63, Pb) > residential area (3.34, Zn; 3.36, Cd; 2.94, Ni; 1.46, Pb) > industrial area (2.74, Zn; 1.78, Cd; 3.01, Ni; 1.45, Pb), indicating that the sediment was “highly contaminated” in the case of Zn and Ni, while for Cd, it was “moderately to highly contaminated,” and for Pb, it was “moderately contaminated.” The pollution is associated with traffic flow in all areas.

Conclusions

Research should be increased to make urban systems more sustainable, reducing their pollution potential and minimizing the delivery of potentially polluting particles into freshwater bodies. The I_geo allows for the determination of a simple index of diffuse pollution state associated with urban sediments.     

Distribution of heavy metals in soils of the Yellow River Delta: concentrations in different soil horizons and source identification

Purpose

The Yellow River Delta, an active land-ocean interaction area, will develop into a large eco-economic region in East China during the coming decade. It is necessary to assess the geochemical features of heavy metals in the soils. The objectives of this research were to evaluate the concentrations and distribution of heavy metals (Cr, Ni, Cu, Zn, Pb, and Cd) in soil profiles of the area and to identify their sources.

Materials and methods

Horizon samples were collected based on pedogenic features from bottom to top in each profile to a depth of 120 cm and a total of 92 samples were collected. The sampling sites were grouped into four lines from inland to coastal area with three land use types (cotton field, cereal field, and wetland). The concentrations of Cr, Ni, Cu, Zn, Pb, and Cd were measured by inductively coupled plasma-mass spectrometry. Iron oxide fractions in the soil were extracted by oxalate-oxalic acid and dithionite-citrate-bicarbonate. X-ray diffraction (XRD) was used to determine the mineral composition of the soils. Multivariate statistical analysis and historical data were employed to identify the possible sources of these heavy metals.

Results and discussion

The mean concentrations of heavy metals were elevated along the Yellow River region and in the southern part of the delta; however, they were generally lower than the Chinese guideline values. As for the depth distribution of heavy metals in soil profiles, the maximum values of Cr, Ni, Cu, Zn, and Cd in middle horizon of cotton field were almost twice than those in surface horizon. The iron oxides and XRD analysis indicated that the trace elements accumulation appeared to be related with the contents of crystalline iron oxide and layer silicates. Historical data from suspended sediments of the Yellow River and principal component analysis (PCA) implied that most of the metals (Cr, Ni, Cu, and Zn) were sourced from natural alluviation and sedimentation.

Conclusions

The Yellow River Delta soils were slightly polluted by heavy metals the Yellow River Delta. The special pedogenic horizon characterized by higher iron oxides and layered silicates minerals in the middle and lower part of the soil profile was found with heavy metals enrichment, which required to be studied further. Suspended sediments transported by the Yellow River were suggested to be one of the major sources for the heavy metals accumulation in the basal soils of this region.     

Modelling trace metal extractability and solubility in French forest soils by using soil properties

Soil/solution partitioning of trace metals (TM: Cd, Co, Cr, Cu, Ni, Sb, Pb and Zn) has been investigated in six French forest sites that have been subjected to TM atmospheric inputs. Soil profiles have been sampled and analysed for major soil properties, and CaCl₂‐extractable and total metal content. Metal concentrations (expressed on a molar basis) in soil (total), in CaCl₂ extracts and soil solution collected monthly from fresh soil by centrifugation, were in the order: Cr > Zn > Ni > Cu > Pb > Co > Sb > Cd , Zn > Cu > Pb = Ni > Co > Cd > Cr and Zn > Ni > Cu > Pb > Co > Cr > Cd > Sb , respectively. Metal extractability and solubility were predicted by using soil properties. Soil pH was the most significant property in predicting metal partitioning, but TM behaviour differed between acid and non‐acid soils. TM extractability was predicted significantly by soil pH for pH < 6, and by soil pH and Fe content for all soil conditions. Total metal concentration in soil solution was predicted well by soil pH and organic carbon content for Cd, Co, Cr, Ni and Zn, by Fe content for Cu, Cr, Ni, Pb and Sb and total soil metal content for Cu, Cr, Ni, Pb and Sb, with a better prediction for acidic conditions (pH < 6). At more alkaline pH conditions, solute concentrations of Cu, Cr, Sb and Pb were larger than predicted by the pH relationship, as a consequence of association with Fe colloids and complexing with dissolved organic carbon. Metal speciation in soil solutions determined by WHAM‐VI indicated that free metal ion (FMI) concentration was significantly related to soil pH for all pH conditions. The FMI concentrations of Cu and Zn were well predicted by pH alone, Pb by pH and Fe content and Cd, Co and Ni by soil pH and organic carbon content. Differences between soluble total metal and FMI concentrations were particularly large for pH < 6. This should be taken into account for risk and critical load assessment in the case of terrestrial ecosystems.     

Fractions of Cu, Cd, and enzyme activities in a contaminated soil as affected by applications of micro- and nanohydroxyapatite

Purpose

With the rapid development of nanotechnology, hydroxyapatite-based nanoparticles have been applied in wastewater and soil remediation. However, limited studies have been conducted on the remediation of heavy metal-contaminated soils by microhydroxyapatite (MHA) and nanohydroxyapatite (NHA). Thus, we investigated the effects of MHA and NHA on soil pH values and fractions of copper (Cu) and cadmium (Cd). The changes of soil enzymes with application of MHA and NHA were also evaluated.

Materials and methods

Pots contained 200 g of the soil with MHA and NHA ranging from 1 % to 5 % incubated for 60 days under greenhouse condition, and maintained at 60 % of soil water holding capacity by adding deionized water. Soil pH, catalase, urease, and acid phosphatase were analyzed at incubation times of 7, 14, 30, and 60 days by chemical assays. The fractions of Cu and Cd were analyzed after 60 days by a sequential extraction procedure.

Results and discussion

Application of MHA and NHA significantly increased soil pH values. Especially, we found for the first time that soil pH values with 3 % (pH?>?7.90) and 5 % (pH?>?8.83) application rates of MHA were larger than that of MHA itself (pH?=?7.71). MHA was more effective than NHA in immobilizing Cu and Cd by significantly decreasing exchangeable fractions of Cu and Cd and transforming them from active to inactive fractions. Soil catalase and urease significantly increased, but acid phosphatase apparently decreased with increasing application rates of MHA. However, three enzymes activities changed slightly for NHA treatments.

Conclusions

MHA was more effective than NHA in immobilizing Cu and Cd. MHA had a more positive effect on soil catalase and urease activities than NHA. Furthermore, Pearson’s correlation coefficients showed that soil pH value was a key factor to influence the bioavailability of Cu and Cd and the activity of soil enzymes. The results of this study provided an efficient method for the remediation of heavy metal-contaminated soils.