Microscale Zn and Pb distribution patterns in subsurface soil horizons: an indication for metal transport dynamics

In many studies on soil pollution, authors conclude that there is no downward migration of metal elements if no evidence for enrichment can be inferred from profiles of total metal contents. We assessed possible transfer of mobile and less mobile metal pollutants to depth in subsurface horizons of a heavy metal contaminated soil, by a study of specific pedofeatures in thin sections by optical microscopy, and their corresponding Zn and Pb distribution patterns by synchrotron‐based X‐ray microfluorescence. In the B horizon (70 cm depth), Zn accumulation was predominantly associated with clay–iron coatings. Strong correlation was found between Zn and Fe (r = 0.94), Zn and Mn (r = 0.75), Zn and Ti (r = 0.84), and Zn and K (r = 0.88), but significant correlation was absent between Zn and Pb. In the C horizon (100 cm depth), clear Pb accumulation was observed in distinct iron coatings, with large correlation coefficients found between Pb and Fe (r = 0.94–0.75), whereas correlation between Zn and Fe was absent. Detected Zn concentrations were small and attributed to the local natural geochemical background. These results were then compared with data of the composition of gravitational soil water collected in other soils from the same study area. Thus, Zn accumulation in the B horizon was ascribed to interception of dissolved Zn²⁺ by negatively charged constituents of clay–iron coatings. In contrast, Pb accumulation in C horizons was related to precipitation of Pb‐bearing iron colloids leading to neoformed, optically pure iron oxyhydroxide crystals and coatings. We demonstrate very localized accumulation of almost immobile Pb which occurs at greater depth than the more mobile Zn. The common, but strongly localized, occurrence of Pb‐bearing iron coatings in the soil groundmass explained the absence of changes in the total Pb concentrations of the C horizon compared with the concentrations in the B horizon.     

Kinetics of speciation of copper,lead, and zinc loaded to soils that differ in cation exchanger composition at low moisture content

Abstract

A better understanding of the fates of heavy metals in wide range of soils is important in improving efficiency of remediation technologies of heavy metals polluted soils. To contribute to this field we studied the kinetics of speciation of copper (Cu), leaf (Pb), and zinc (Zn) in six soils differed in major cation exchanger composition. Soluble salts of Cu, Pb, and Zn were loaded to the soils, incubated at field moisture contents, and the change in chemical forms of the metals was traced by sequential extraction. In Inceptisols predominated by 2:1 layer silicates and poorly crystalline iron oxides, the added Cu and Pb were found mostly in exchangeable and oxide bound fractions, with decreasing and increasing proportion of the former and the latter during 50 days after addition, respectively. In allophanic and humic Andisols, about 50 to 70% of the total Cu and Pb was found in oxide bound fraction with a significant amount in organically complexed fraction in the latter. The amounts of Cu and Pb in each fraction varied only slightly with time in these soils. The proportion of oxide bound Cu arid Pb was relatively low in a kaolinitic Ultisol irrespective of its higher iron oxide content. Zinc was found mostly in exchangeable and soluble fractions except in Andisols. Low crystallinity of oxide minerals as well as their amount is important factors determining heavy metal retaining capacity of soils. The exchangeable and oxide bound heavy metals should be treated separately in models simulating removal of heavy metal cations by washing and electrokinetic methods.     

Fractionation and Distribution of Metals in Guadiamar River Sediments (SW Spain)

Traditionally, the Guadiamar River (Seville, Southwest Spain) has received pollution from two different sources, in its upper section, from a pyrite exploitation (Los Frailes mine) and, in its lower section, from untreated urban and industrial wastes and from intensive agricultural activities. In 1998, the accidental spillage of about 6 million m³ of acid water and sludge from mine tailings to Guadiamar River worsened the pollution of an already contaminated area. The main polluting agents of the spillage were heavy metals. The total concentration of a metal provides scarce information about the effects on environmental processes or about the toxicity of the sediment samples. A more sophisticated fractionation of the sediment samples based on a species distribution can help to understand the behaviour and fate of the metals. This article describes a distribution study of the metals Al, Cd, Cu, Fe, Mn, Pb and Zn by fractionation analysis of sediments from eleven sample sites alongside the Guadiamar Riverbed. The samples were collected in summer 2002, four years after the spillage and after the area had been cleaned. Sequential extraction analysis resulted in the definition of four fraction categories: exchangeable metal (the most available fraction), reducible metal (bound to hydrous oxides of Fe and Mn), oxidizable metal (bound to organic matter and sulphides) and a residual fraction (bound to minerals). Significant increases in the available fraction of several potentially toxic metal ions like Cd, Mn and Zn were found. The distribution pattern was variable along the River. At the site closest to the mineworks, the soluble forms of Cd, Mn and Zn were significantly more abundant that those downstream. Cu and Pb were present in the reducible fraction while Fe was present associated in the residual fraction.     

Retention of Metals in Agricultural Soils After Amending with MSW and MSW-Biosolids Compost

The goal of this study was to measure the As, Cu, Fe, Pb and Zn contents of soils amended with municipal solid waste (MSW) and MSW-biosolids compost and to determine the long-term transport of these metals to lower soil horizons. Lead, Cu, Cd and Zn contents in the composts were 3–20 times more concentrated in the compost compared to the soil at the Calverton, NY, U.S.A. farm. As a result, Pb, Cd, Cu and Zn were elevated in the upper 5 cm soil layer following compost application and the metal enrichment was proportional to the amount of compost applied (21–62 Mg ha^-1). In addition, Pb, As and Cu contents of the non-compost amended Calverton soils were enriched above the tillage depth (20–25 cm). Cu, Pb and As enrichment was attributed to the historical use of sodium arsenite, lead arsenate and copper sulfate insecticides and fungicides. Results of the metal analyses of soil cores collected 16 and 52 months following compost application showed that Cu, Zn and Pb remained confined to the upper 5 cm soil layer. The low water extractable fraction of these metals in MSW and MSW-biosolids compost was a major factor limiting the transport of these metals to lower soil horizons. In contrast, Cd leaching from the upper 0–5 and 5–10 cm soil layers was continuous over the 52 month study period and was attributed primarily to the presence of soluble Cd in phosphate fertilizer initially applied to the Calverton farm soil.     

Distribution of Trace Elements in Soils from the Sudbury Smelting Area (Ontario,Canada)

The sequential extraction procedure proposed by the European Commission Measurement and Testing Programme, combined with Scanning Electron Microscopy and Energy Dispersive X-ray Analysis(SEM/EDS), was applied to identify and quantify the chemical andmineralogical forms of Cu, Ni, Fe, Mn, Zn, Pb, Cr and Cd presentin the topsoil from a mining and smelting area near Sudbury (Ontario, Canada). The possible mobility of the chemical forms was also assessed. The metal fractions: (1) soluble and exchangeable, (2) occluded in manganese oxides and in easily reducible iron oxides, (3) organically bound and in form of sulphides, (4) residual mainly present in the mineral lattice structures were separated. Cu and Ni were the major metallic contaminants, occurring in soils in broad ranges of concentrations: Cu 11–1890 and Ni 23–2150 mg kg^-1. Cu was uniformly distributed among allthe extracted fractions. Ni was found associated mainly withthe residual forms, accounting for 17–92%, with an averageof 64%, of the total Ni present in the soils. Fe, Mn, Zn,Pb, Cr and Cd, while occurring in most analysed samples innormal soil concentrations, were primarily held in theresidual mineral fraction (on average >50%). The solubleand exchangeable forms made a small contribution (≤8.1%)to the total content of metals extracted. At least 14% ofthe total Cd, Mn and Pb was mobilised from the reducibleforms. The oxidizable fraction assumed mean values higher than10% only for Pb and Zn. Statistical treatment of the experimental data showed significant correlations between totalmetal content of the soils, some soil properties such as pH value, clay and organic matter content, and metal concentrationsin the various fractions. SEM/EDS analysis showed Fe in form ofoxides and sulphides in soils and Cu, Ni, Mn, Zn and Cr in association with iron oxides. Numerous black carbonaceous particles and precipitates of aluminium fluoride salts, observedin the solid residue left after `total’ digestion, were found tocontain Fe, Ni and Cr.     

Spatial distribution of soil heavy metal concentrations as indicator of pollution sources at Mount Križna (Great Fatra,central Slovakia)

The objective of this study was to test the suitability of a simple approach to identify the direction from where airborne heavy metals reach the study area as indication of their sources. We examined the distribution of heavy metals in soil profiles and along differently exposed transects. Samples were taken from 10 soils derived from the same parent material along N-, S-, and SE-exposed transects at 0—10, 10—20, and 20—40 cm depth and analyzed for total Al, Cd, Cr, Cu, Fe, Mn, Ni, Pb, and Zn concentrations. The heavy metal concentrations at 0—10 cm were larger than background concentrations in German arable soils except for Cr (Cd: 0.6—1.8 mg kg^—1; Cr: 39—67; Cu: 40—77; Ni: 87—156; Pb: 48—94; Zn: 71—129; Fe: 26—34 g kg^—1; Mn: 1.1—2.4). Decreasing Cd, Cu, Mn, and Pb concentrations with increasing soil depth pointed at atmospheric inputs. Aluminum and Ni concentrations increased with soil depth. Those of Fe, Cr, and Zn did not change with depth indicating that inputs at most equalled leaching losses. The Pb accumulation in the surface layer (i.e. the ratio between the Pb concentrations at 0—10 to those at 20—40 cm depth) was most pronounced at N-exposed sites; Pb obviously reached Mount Križna mainly by long-range transport from N where several industrial agglomerations are located. Substantial Cd, Cu, and Mn accumulations at the S- and SE-exposed sites indicated local sources such as mining near to the study area which probably are also the reason for slight Cr and Zn accumulations in the SE-exposed soils. Based on a principal component analysis of the total concentrations in the topsoils four metal groups may be distinguished: 1. Cr, Ni, Zn; 2. Mn, Cd; 3. Pb (positive loading), Cu (negative loading); 4. Al, Fe, indicating common sources and distribution patterns. The results demonstrate that the spatial distribution of soil heavy metal concentrations can be used as indication of the location of pollution sources.     

Soil Factors Affecting Heavy Metal Solubility in Some New Zealand Soils

Heavy metal contamination of soils is usually quantified and guidelines set solely on the basis of total heavy metal content. However, it is recognised that water soluble heavy metal concentrations may provide a better indication of the potential risk that heavy metals may pose to the soil environment. The aim of this study was to use a semi-empirical model based on the competitive adsorption of metal and H⁺ ions [dependent on solution pH, total metal content, total carbon content and soil oxide content] to predict water soluble Cu, Cr, Cd, Pb, Ni and Zn concentrations in a range of field contaminated soils. The results of multiple linear regressions showed that basic soil properties could predict 85, 72, 66, 78, 50 and 75% of the variation in soluble Ni, Cu, Cr, Pb, Cd and Zn concentrations respectively. Water soluble metal concentrations were best predicted using empirical linear regressions which included total metal content, while the importance of other soil properties such as soil pH, total carbon and oxalate extractable Fe and Al oxides varied between metals. The models have the potential to provide valuable information on metal availability in contaminated soils and offer an indication of the potential risk a metal may pose to a given soil environment, along with providing a basis for developing soil quality guidelines for the prevention, investigation and clean-up of soil metal contamination.     

Fluoro‐mobilization of metals in a Slovak forest soil affected by the emissions of an aluminum smelter

Depositions originating from a central Slovak Al smelter may increase metal solubility in adjacent soils because they contain F (mainly HF). The reason for fluoro‐mobilization of metals may be the formation of soluble fluoro‐metal complexes or the mobilization of organic matter and subsequent formation of organo‐metal complexes. The objectives of our work were (1) to assess the extent of metal mobilization by fluoride in a Slovak Lithic Eutrochrept affected by the emissions of an Al smelter and (2) to model the dissolved metal species with the help of a chemical equilibrium model (MINEQL+). The O (Moder), A, and B horizons were equilibrated with solutions at F concentrations of 0, 0.9, 2.7, and 9.0 mmol l^—1. In the extracts, the concentrations of Al, Ca, Cd, Cr, Cu, Fe, K, Mg, Mn, Ni, Pb, Zn, dissolved organic carbon (DOC), free and complexed F, and the pH and electrical conductivity (EC) were determined. The heavy metal concentrations in the O horizon (Cd: 0.99, Cr: 18.0, Cu: 44, Ni: 26, Pb: 110, and Zn: 84 mg kg^—1) were 2.5 to 9 times larger than those in the A and B horizons. The concentrations of H₂O‐soluble F decreased from the O (261 mg kg^—1) to the A (103 mg kg^—1) and B horizon (92 mg kg^—1). In batch experiments increasing addition of F increased the equilibrium concentrations of Al, Cr, Cu, Fe, Ni, Pb, and DOC in all samples, of Cd in the A, and of K in the B horizon. At the same time the concentrations of complexed F and pH increased whereas EC decreased. Chemical equilibrium modelling indicated that the mobilizing effect of F resulted from the formation of fluoro‐Al complexes and organo‐complexes of all other metals.     

Bulk sediment bioassays with five species of fresh-water oligochaetes

The fluxes of metals (Na, K, Ca, Mg, Fe, Mn, Al, Cu, Zn, Pb, Cd, Cr, and Ni) in two spruce forest soils in S. Sweden were quantified using the lysimeter technique. Amounts in precipitation (dry and wet), throughfall, litterfall and annual accumulation in biomass were also quantified, as well as stores in soil and biomass. The metal concentrations of the soil solutions varied greatly according to season. The leaching of some metals (Fe, Cu, Pb, Cr, and organic forms of Al) was associated with the leaching of organic matter. These complexes were leached from the A horizon in considerable amounts. They were precipitated in the upper B horizon and only small amounts were transported further downward. By contrast, the leaching of Na, Mg, Ca, Mn, Cd, Zn, Ni, and inorganic forms of Al increased with increasing soil depth. The concentrations of these metals also increased with increasing soil solution acidity. The highest concentrations were often found at the transition to the C horizon. The amounts of Na, K, Mg, Ca, Mn, Al, Zn, Cd, Cr, and Ni leached from the rooting zone were found to be larger than the amounts deposited from the atmosphere, the main source of these metals being the mineral soil. The reverse was true of Ph, Cu, and Fe, the sink being the upper part of the B horizon.     

PARTITIONING OF HEAVY METALS IN PODZOL SOILS CONTAMINATED BY MINE DRAINAGE WATERS,DALARNA, SWEDEN

The discharge of acidic mine drainage waters onto a hillslope in Dalarna, central Sweden, has lead to the contamination of the podzol soils with Cu, Fe, Ni, Pb, Zn and sulfate. Samples from contaminated and reference soils have been collected for chemical and mineralogical analyses. Jarosite is identified by x-ray diffraction analysis as a precipitate in the upper horizons (A, E, B) of the contaminated soils, where the soil acidity (pH_KCl～2.6) promotes jarosite stability. The sequential chemical extraction of soil samples indicates that, in the reference A horizon, Cu, Pb, Ni and Zn are bound primarily to cation exchange sites and organic matter. In the A horizon of the contaminated soils closest to the rock dump, metal partitioning is dominated by the Fe oxide fractions, despite the high organic matter content; Pb is almost completely bound to crystalline Fe oxides, possibly adsorbed to Fe oxides or occuring in a jarosite solid solution. In the reference B and C horizons, Cu, Ni and Zn are primarily adsorbed/coprecipitated in the Fe oxide fractions, while Pb remains with a large fraction bound to organic matter. In the Fe-rich B horizon of the contaminated soils, the partitioning of the metals in cation exchange sites and to organic matter has greatly increased relative to the reference soils, resulting from the mobilization of organo-metal complexes down the profile.     

Heavy Metal Contamination in Peach Trees Irrigated with Water from a Heavily Polluted Creek

This study was conducted to characterize the heavy metal contamination in the soils of peach orchards irrigated with water from Nilüfer creek, which is heavily polluted by industrial and municipal wastes. Twenty-one peach orchards with 3 different cultivars in 7 orchards each located along Nilüfer creek were monitored in the experiment. To determine levels of pollution, soils and aboveground parts of the trees were sampled and analyzed for iron (Fe), manganese (Mn), zinc (Zn), copper (Cu), cobalt (Co), nickel (Ni), chromium (Cr), lead (Pb), and cadmium (Cd). Total amounts of Ni and Cr were found to be at the excessive levels in soils. Extractable Ni concentration decreased with increasing pH and CaCO₃ content in soils. Leaf metal contents were generally at tolerable levels, but Ni and Pb accumulated to toxic levels in different parts of the fruit (flesh and peel). Except for Fe and Ni, plant concentrations of the metals did not correlate with their total and DTPA-extractable concentrations in the soils. There was no significant difference among the cultivars in accumulation of heavy metals.     

Transport and distribution of heavy metals in Cauvery river

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.     

Leaching of Metals in Coastal Technosols Triggered by Saline Solutions and Labile Organic Matter Removal

This study aims to understand the influence of salinity and labile organic matter removal on the fate and behavior of metals in coastal technosols. Two technosol cores were collected near the Lebanese shore. The cores were sectioned into layers; each layer was characterized for pH, salinity, electric conductivity, labile and total organic matter, grain size, and total and oxalate-extractable metals. Consequently, two saline solutions were used in desorption experiments to understand the role of ionic strength and labile organic matter on metal release. The results showed that the technosol layers were highly heterogeneous; most layers were enriched with Fe, Zn, Pb, and Cu. The mineralogical investigations showed that the metals, notably Fe, were not present as crystalline minerals, rather big percentages of the metals were found in amorphous or poorly crystalline phases. Desorption experiment showed that Mg release was dependent on salinity and organic matter in both technosols, while Pb release was dependent on both factors only in one. Additionally, Zn and Cu were associated to organic matter, and their release was conditioned by the removal of labile organic matter; iron was primarily found as amorphous or poorly crystalline phases, and salinity had a major role in its release. The role of ionic strength and labile organic matter removal on the behavior of metals in technosols was demonstrated. Finally, understanding metal dynamics between the solid and liquid compartments in technosols, especially where salt deposition occurs, is important to reduce unwanted metal leaching to groundwater or seawater and transfer to biota.     

云南滇池沉积物中重金属的形态分布特征

Fractionation of heavy metals in sediments can help in understanding potential hazards of heavy metals. The present study analyzed total concentrations and fractions of selected heavy metals （Cd, Cr, Cu, Pb, and Zn） in surface sediments from Dianchi Lake, Yunnan Province, China, as well as factors that may affect distributions of the various heavy metal fractions. Total concentrations of the heavy metals decreased in the order Zn 〉 Cu 〉 Pb 〉 Cr 〉 Cd. These heavy metals, except Cr, were much higher than their background levels, indicating that Dianchi Lake was polluted by Cd, Zn, Pb, and Cu. Cadmium occurred mainly as the non-residual fraction （sum of the HOAc-soluble, reducible, and oxidizable fractions） （97.6%）, and Zn （55.7%） was also predominantly found in the non-residual fraction. In contrast, most of the Cr （88.5%）, Pb （81.8%）, and Cu （59.2%） occurred in the residual fraction. Correlation analysis showed that total heavy metal concentrations, organic matter and reducible Fe were the main factors affecting the distributions of the various heavy metal fractions. In the Walhai section of Dianchi Lake （comprising 97% of the lake area）, the concentrations of Cd, Zn, Pb, and Cu in the non-residual fraction were significantly lower （P ≤ 0.01 or 0.05） than those of the Caohal section （3% of the lake area）. This indicated that potential heavy metal hazards in the Caohai section were greater than the Waihai section.     

Soil contamination in the zone affected by waste products of Tin Ore Processing in the Khabarovsk region

The degree of soil contamination in the impact zone of the Solnechnyi Tin Ore Processing Plant in the Solnechnyi district of the Khabarovsk region was evaluated. It was shown that the air contamination by the waste products of the ore-processing plant is extremely high with respect to the concentrations of toxic dust and heavy metals. The maximum concentrations of these contaminants exceed the background values by 16–80 times. The bulk contents of Pb, Zn, Cu, As, and Hg in the upper soil horizons within the impact zone exceeded the maximum permissible concentrations and the background values by 2–90 times. Abnormally high concentrations of Zn, As, and Pb were observed not only in the surface 10–cm-thick soil layer but also in the underlying (10–20 cm) horizon. The soil contamination transformed the geochemical sequence of heavy metals typical of the background soils (Zn > Pb > As > Cu > Hg) into a new sequence (As > Pb > Cu > Zn > Hg). The statistical data proved that the intensity of the migration of the heavy metals in the soils decreases with a rise in the soil humus content and a drop in the soil acidity. This should be taken into account in the elaboration of soil-protective measures in the investigated region.     

杭州市城市土壤中重金属、磷和其它元素的特征

Health implications of inhaling and/or ingesting dust particles with high concentrations of heavy metals from urban soils are a subject of intense concern. Understanding the geochemistry of these metals is key to their effective management. Total concentrations of heavy metals, phosphorus (P) and 8 other elements from topsoil samples collected at 82 locations in Hangzhou City were measured to: a) assess their distribution in urban environments; and b) understand their differentiation as related to land use. Metal mobility was also studied using a three-step sequential chemical fractionation procedure. About 8.5%, 1.2%, 3.6%, 11.0% and 30.3% of the soil samples had Cd, Cr, Cu, Pb, and Zn concentrations, respectively, above their allowable limits for public and private green areas and residential use. However, in commercial and industrial areas, most samples had metal concentrations below their allowable limits. Statistical analyses revealed that the 16 measured elements in urban soils could be divided into four groups based on natural or anthropic sources using a hierarchical cluster analysis. Additionally, Cu, Pb, and P showed similar spatial distributions with significant pollution in commercial zones, suggesting vehicle traffic or commercial activities as dominant pollutant sources. Also, Cd, Co, Cr, Ni, Zn, Mn and Fe had the highest concentrations in industrial locations, signifying that industrial activities were the main sources of these seven metals. Moreover, the data highlighted land-use as a major influence on heavy metal concentrations and forms found in topsoils with large proportions of soil Cd, Co, Cr, and Ni found in residual fractions and soil Cu, Pb and Zn mainly as extractable fractions.     

Profile Distributions of Lead,Zinc, and Copper in Dystric Cambisols Developed from Granite and Gneiss of the Sudetes Mountains,Poland

Total contents of Pb, Zn and Cu were examined in twenty-five soilprofiles of forested Dystric Cambisols developed from granite andgneiss in the area of the Sudetes Mountains (SW Poland). Sequential extraction of heavy metals was also carried out to study relations between metal content and soil compounds. Profile distribution differed among the metals examined: Pb concentrations decreased gradually from surface with depth, whereas those of Zn increased with depth of soil profile, obtaining their maximum in the bedrock horizon. Cu was found to accumulate in topsoil and decrease with depth, but showed secondary increase of the concentration in bedrock. Organic matter was found to be a crucial factor of Pb binding and distribution, while iron oxides played the most important rolein Zn binding. Both organic matter and oxides were important factors of Cu distribution. The results of sequential extractionshow that all studied elements are mobile under strong acidicconditions in investigated Cambisols. Thus, total contents of Zn and Cu in bedrock cannot be used as geochemical background or as reference levels for assessing the contamination of soilsurface with these metals.     

巢湖表层沉积物中重金属的分布及污染评价

对巢湖湖区不同位点的表层沉积物中的Fe、Cr、Pb、Cu、Co、Zn、Ni7种重金属含量进行的分析表明,湖泊沉积物中重金属含量分布呈现一定的区域特征,由于巢湖西半湖靠近合肥市区,大量的工业废水和生活污水通过河道排入巢湖,引起西半湖区中重金属含量高于东半湖区。采用富集因子法和地积累指数法对巢湖沉积物重金属污染现状进行了评价,结果表明,巢湖沉积物中存在Pb、Cu污染,个别地区已相当严重,并呈现沿湖心区至东半湖区逐渐降低趋势。研究表明,两种方法均能对人为污染行为做出较为科学的评价,且两种方法得到的评价结果基本一致。由于重金属元素有很强的毒性,并且能够在食物链中传递,有关部门应及早从流域环境综合规划入手,对重金属污染问题采取有力的控制对策,保护沿湖地区居民免受危害。此外,对巢湖表层沉积物中重金属污染物来源进行了初步分析,据分析结果判断,巢湖沉积物中重金属总量Co、Fe、Cr的来源相似,Zn和Cu的来源相似。     

Role of micronutrients on quantitative traits and prospects of its accumulation in linseed (Linum usitatissimum L.)

The adequate growth of plants can be achieved only by a balanced ratio of biologically active nutrients in soil along with its readily availability. Linseed seems to be an advantageous secondary oilseed crop widely used in industrial purposes, which can serve additional purpose of phytoextraction of heavily infested soils with heavy metals. In this study, we have made an effort to find out the optimum dose of heavy metals necessary as micronutrients like copper (Cu), iron (Fe) and zinc (Zn) for the enhancement of linseed yield along with the distribution of heavy metals in different plant parts. Quantitative enhancement in different traits of linseed plant due to Cu, Fe and Zn fertilization especially for capsules per plant after maturity suggested positive association between heavy metal supply and morphological traits, which indirectly enhanced seed yield. There was a positive correlation between Zn supply and seed yield. In the treatments with Cu and Fe fertilization, seed yield was positively correlated to plant height, capsules per plant and seeds per five capsules. According to this study, it is concluded that linseed has the ability to accumulate majorly Fe followed by Cu and Zn.     

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.