Immobilization of soil copper using organic and inorganic amendments

This experiment aimed to immobilize Cu in polluted agricultural soils via the application of agrochemicals to reduce its bioavailability to plants. A greenhouse pot experiment was established using a Cu contaminated vineyard topsoil collected from a farm in Greece. The soil was mixed with inorganic [i.e., zeolite (Z), Al‐oxide (AX), Mn‐oxide (MX), and phosphate rock (PR)] as well as organic amendments [i.e., activated charcoal (AC), commercial peat soil material (CP), and compost from olive oil processing wastes (COW)] with an application rate of 2.5% and cultivated by corn (Zea maize). After plant harvesting, Cu was measured separately in the aboveground biomass and roots, respectively, whereas the soil samples were analyzed for DTPA‐extractable and geochemical fractions of Cu (soluble + exchangeable fraction, sorbed and carbonate fraction, Fe‐/Mn‐oxides fraction, and organic fraction). The immobilizing agents, except MX, reduced the soluble plus exchangeable Cu in the treated soil. The lowest concentrations of the soluble plus exchangeable Cu occurred in the soil amended with AC followed by CP, AX, COW, PR, and Z, respectively. The amendments decreased the uptake of Cu by corn. Concentrations of Cu were between 11 and 38% lower in the above ground biomass and 19 and 48% lower in the roots than the control. The organic amendments were more effective than the inorganic additives. The AC was the most effective organic additive and AX was the most effective inorganic amendment.     

Verhalten von Schwermetallen in Böden 1. Untersuchungen zur Schwermetallmobilität

Behaviour of heavy metals in soils. 1. Heavy metal mobility 158 soil samples with widely varying composition were analysed for their total, EDTA, DTPA and CaCl₂ extractable contents of Cd, Zn, Mn, Cu and Pb. By means of single and multiple regressions the relations between the different heavy metal fractions and the pH, organic carbon and clay content were considered. The correlations between the total, EDTA and DTPA extractable contents are very close, whereas the CaCl₂ extractable contents are not or only weakly correlated with these fractions. According to these statistical results the former fractions are considered to be the total quantity (total content) and the reactive quantity (EDTA and DTPA extractable contents) of the heavy metals, whereas the CaCl₂ extractable fraction represents the mobile fraction of the heavy metals in soils. The multiple regressions show that the mobile content of heavy metals is closely correlated with each of the quantity fractions and with soil pH. In the same way the proportion of the mobile fraction (in %) of the total, EDTA and DTPA extractable heavy metal content of the soil samples is closely related to the soil pH. Hereby the proportion of the mobile content of the various elements increases in the pH range 6,5 - 3 below element-specific threshold pH values (in brackets) in the order Cd (6,5) > Mn (5,7) > Zn (5,3) > Cu (4,5) > Pb (3,5). In the pH range 6,5 - 7,5 mainly Cu and to a lesser degree also Pb show an increasing mobility due to the influence of soluble organic substances.     

Prediction of available heavy metals by six chemical extractants in a sewage sludge‐amended soil

Abstract

In a field experiment conducted during three years in a sandy‐loam, calcareous soil, one aerobically digested sewage sludge (ASL) and another anaerobically digested sewage sludge (ANSL) were applied at rates of 400, 800, and 1,200 kg N/ha/year, and compared with mineral nitrogen fertilizer at rates of 0, 200, 400, and 600 kg N/ha/year in a cropping sequence of potato‐corn, potato‐lettuce, and potato, the first, second, and third year, respectively. Results showed that the highest values of soil extractable metals were obtained with aqua regia, whereas the lowest levels with DTPA. All metal (Zn, Cu, Cd, Ni, Pb, and Cr) gave significant correlations between metal extracted with the different extractants and metal loading applied with the sludges. The metal extractable ion increased over the control for Zn, Cu, Cd, Ni, Pb, and Cr extracted with DTPA, EDTA (pH 8.6) and 0.1 N HC1, for Zn, Cd, Ni, Pb, and Cr extracted with EDTA (pH 4.65) and AB‐DTPA, and for Zn, Cd, Ni, and Cr extracted with aqua regia. The level of metal‐DTPA extractable resulted highly correlated with that obtained by the other methods, except the Ni‐aqua regia extractable. The soil extractable elements which showed significant correlations with metals in plant were: Zn, Cu, Cd, and Ni in potato leaves, Cd, Ni, and Pb in corn grain, and Zn and Cd for lettuce wrapper leaves. In general, all the chelate based extractants (DTPA, EDTA pH 4.6, EDTA pH 8.6, AB‐DTPA) were equally useful as indicator of plant available metals in the soil amended with sludge.     

Compost use in viticulture: Effect on heavy metal levels in soil and plants

Abstract

The purpose of this study was to examine the long‐term effect of compost application on the heavy metal content in soil, leaves, and fruit of grape (Vitis vinifera). Two types of compost were tested in a vineyard. One was compost with a low heavy metal content, which was derived from sewage sludge and bark (SB compost). The other type was compost with a higher concentration of metals, which was derived from municipal solid waste (MSW compost). For 6 years, the levels of zinc (Zn), copper (Cu), nickel (Ni), lead (Pb), cadmium (Cd), and chromium (Cr) in their total (aqua regia digestion), EDTA‐extractable, and DTPA‐extractable forms were monitored in soil, leaves, musts, and wines. The resulting data clearly demonstrate that SB compost did not cause any significant increase in heavy metal levels in the soil and the plants. Thus, this type of compost can be used for soil fertilization with no danger either to the environment or to crops. In contrast, the use of MSW compost caused a significant accumulation of Ni, Pb, Cd, and Cr in the soil, in vegetation, and in musts. Skin‐contact fermentation dramatically decreased the heavy metal content of the wines. The concentration of heavy metals in plant tissues was found to be positively correlated with the DTPA‐extractable form of the metals in the soil, but not correlated with the total or the EDTA‐extractable forms.     

Chemical and organic immobilization treatments for reducing phytoavailability of heavy metals in copper‐mine tailings

This study was conducted to evaluate the efficiency of diammonium phosphate (DAP), agricultural limestone (lime), and green‐waste compost mixed with 30% treated sewage sludge (GCS) applied alone or in combination as chemical immobilization treatment using tomato as a test crop. Mine waste was collected from an abandoned copper‐mine tailing site at Mynydd Parys, Anglesey (UK). Lime was applied at the rate of CaCO₃ equivalent (CCE, pH = 7), DAP at the rate of 23 g P per kg substrate, and 10% by weight, GCS as sole application. Half rate of each amendment was also tested as a combined treatment and an untreated substrate (control). Plant‐available metals (Cd, Cu, Fe, Pb, and Zn) were measured in substrate with conventional diethylenetriaminepentaacetic acid (DTPA) and sequential Ca(NO₃)₂ extraction. Plant–dry biomass yield was significantly (p < 0.001) increased by the combined application of all the three amendments while sole application of DAP reduced yield by 4‐fold compared to unamended soil probably due to P toxicity. Addition of lime reduced the DTPA‐extractable Cu, Fe, and Zn by 75%, 81%, and 85%, respectively, while Pb availability was reduced by 88% in combined DAP + lime + GCS treatment compared to control. The extraction capacity of DTPA was higher than that of Ca(NO₃)₂ by 3‐fold for Cu and Fe, 8‐fold for Pb, and 2‐fold for Zn. The leaf‐tissue concentrations of Cu and Fe were reduced by 77% and 83% in the lime + GCS amendment, respectively, while both Pb and Zn were reduced by 89% and 33%, respectively, in substrate treated with the combined application of all three amendments. These results suggest that alkaline amendments (both lime and GCS) were effective in reducing the phytoavailability of Cu, Fe, and Zn while DAP mixed with either GCS or lime was effective in reducing Pb availability.     

Comparison of routine soil tests and EPA method 3050 as extractants for heavy metals in Delaware soils

Abstract

Agricultural use of sewage sludges can be limited by heavy metal accumulations in soils and crops. Information on background levels of total heavy metals in soils and changes in soil metal content due to sludge application are; therefore, critical aspects of long‐term sludge monitoring programs. As soil testing laboratories routinely, and rapidly, determine, in a wide variety of agricultural soils, the levels of some heavy metals and soil properties related to plant availability of these metals (e.g. Cu, Fe, Mn, Zn, pH, organic matter, texture), these labs could participate actively in the development and monitoring of environmentally sound sludge application programs. Consequently, the objective of this study was to compare three soil tests (Mehlich 1, Mehlich 3, and DTP A) and an USEPA approved method for measuring heavy metals in soils (EPA Method 3050), as extractants for Cd, Cu, Ni, Pb and Zn in representative agricultural soils of Delaware and in soils from five sites involved in a state‐monitored sludge application program.

Soil tests extracted less than 30% of total (EPA 3050) metals from most soils, with average percentages of total metal extracted (across all soils and metals) of 15%, 32%, and 11% for the Mehlich 1, Mehlich 3, and DTPA, respectively. Statistically significant correlations between total and soil test extractable metal content were obtained with all extractants for Cu, Pb, and Zn, but not Cd and Ni. The Mehlich 1 soil test was best correlated with total Cu and Zn (r=0.78***, 0.60***, respectively), while the chelate‐based extractants (DTPA and Mehlich 3) were better correlated with total Pb (r=0.85***, 0.63***). Multiple regression equations for the prediction of total Cu, Ni, Pb, and Zn, from soil test extractable metal in combination with easily measured soil properties (pH, organic matter by loss on ignition, soil volume weight) had R² values ranging from 0.41*** to 0.85***, suggesting that it may be possible to monitor, with reasonable success, heavy metal accumulations in soils using the results of a routine soil test.     

Mehlich‐1‐ and DTPA‐extractable lead in soils in relation to soil properties

Abstract

Mehlich‐1 and DTPA extractants are frequently used to predict metal availability in soils. Metal extractability by the acid or chelate extractant reflects the metal characteristics and metal‐soil interactions. In this study, samples of eight topsoils from the southeastern United States were incubated with added lead (Pb) at the rate of 40 mg#lbkg^‐1. After five months in the greenhouse, Mehlich‐1 and DTPA extractants were employed to extract Pb in both metal‐amended and natural soils. For the natural soils, Pb concentration in the DTPA extractant was always higher than that in the Mehlich‐1 extractant. This indicates that the DTPA chelate extractant is able to dissolve some Pb in soils which is not solubilized by protons. The negative correlation found between Mehlich‐1‐extractable Pb and soil clay content might result from two mechanisms: i) strong association between Pb and soil surfaces, or ii) readsorption of Pb during extraction. None of the correlations between DTPA‐extractable Pb and soil properties was significant, suggesting that the DTPA‐extractable Pb is not heavily dependent on soil properties. The DTPA extractant showed a high ability to solubilize Pb in the natural soils possibly due to a high affinity of Pb for soil organic matter.     

Extractability and plant uptake of heavy metals in alum shale soils

Abstract

Fifty soil samples (0–20 cm) with corresponding numbers of grain, potatoes, cabbage, and cauliflower crops were collected from soils developed on alum shale materials in Southeastern Norway to investigate the availability of [cadmium (Cd), copper (Cu), zinc (Zn), lead (Pb), nickel (Ni), and manganese (Mn)] in the soil and the uptake of the metals by these crops. Both total (aqua regia soluble) and extractable [ammonium nitrate (NH₄NO₃) and DTPA] concentrations of metals in the soils were studied. The total concentration of all the heavy metals in the soils were higher compared to other soils found in this region. Forty‐four percent of the soil samples had higher Cd concentration than the limit for application of sewage sludge, whereas the corresponding values for Ni, Cu, and Zn were 60%, 38%, and 16%, respectively. About 70% the soil samples had a too high concentration of one or more of the heavy metals in relation to the limit for application of sewage sludge. Cadmium was the most soluble of the heavy metals, implying that it is more bioavailable than the other non‐essential metals, Pb and Ni. The total (aqua regia soluble) concentrations of Cd, Cu, Zn, and Ni and the concentrations of DTPA‐extractable Cd and Ni were significantly higher in the loam soils than in the sandy loam soils. The amount of NH₄NCyextractable metals did not differ between the texture classes. The concentrations of DTPA‐extractable metals were positively and significantly correlated with the total concentrations of the same metals. Ammonium nitrate‐extractable metals, on the other hand, were not related to their total concentrations, but they were negatively and significantly correlated to soil pH. The average concentration of Cd (0.1 mg kg^‐1 d.w.) in the plants was relatively high compared to the concentration previously found in plants grown on the other soils. The concentrations of the other heavy metals Cu, Zn, Mn, Ni, and Pb in the plants were considered to be within the normal range, except for some samples with relatively high concentrations of Ni and Mn (0–11.1 and 3.5 to 167 mg kg‘¹ d.w., respectively). The concentrations of Cd, Cu, Zn, Ni, and Mn in grain were positively correlated to the concentrations of these respective metals in the soil extracted by NH₄NO₃. The plant concentrations were negatively correlated to pH. The DTPA‐extractable levels were not correlated with plant concentration and hence DTPA would not be a good extractant for determining plant availability in these soils.     

苏南地区土壤重金属向蔬菜的迁移研究

Vegetable fields in peri-urban areas receive large amounts of extraneous heavy metals because of rapid urbanization and industrialization in China. The concentrations of Cu, Zn, and Pb in 30 soil samples and 32 vegetable samples, collected from 30 different sites in southern Jiangsu Province of China, were measured and their transfer from soil to vegetable was determined. The results showed that the soil samples had wide ranges of pH (4.25-7.85) and electrical conductivity (EC) (0.24-3.42 dS m^-1). Among the soil samples, there were four soil samples containing higher Cu and two soil samples containing higher Zn concentrations than those specified in the Chinese Soil Environmental Quality Standard II. However, no vegetable sample was found to contain a high level of Cu or Zn. In contrast, one vegetable sample contained 0.243 mg Pb kg^-1 FW, which was above the Chinese Food Hygiene Standard, whereas the corresponding soil Pb concentration was lower than the Chinese Soil Environmental Quality Standard II. The transfer coefficients of Cu of all vegetable samples exceeded the suggested coefficient range, implying that extraneous Cu had high mobility and bioavailability to vegetables. There was no significant correlation between extractable soil heavy metal concentrations with four kinds of extractants and soil pH, EC, heavy metal concentrations in vegetables and soils, except that soil pH correlated well with the extractable soil Cu, Zn, and Pb concentrations with 1.0 mol L^-1 NH₄NO₃. Moreover, diethylenetriamine pentaacetic acid (DTPA) extraction method was a more effcient method of extracting heavy metals from the soils independent of soil pH and EC than other three methods used.     

不同钝化剂对Cu、Cr和Ni复合污染土壤的修复研究

利用盆栽试验研究了不同钝化剂(沸石、牡蛎壳、鸡蛋壳、硅藻土和聚丙烯酰胺(PAM))对生长在重金属污染土壤上的青菜(Brassica chinensis L.)生物量、重金属吸收以及超氧化物歧化酶的活性(SOD)和丙二醛(MDA)含量的影响,同时,通过对土壤p H和土壤重金属提取态的分析,探讨了钝化剂影响青菜生物量和重金属吸收的可能原因。结果表明:钝化剂加入可显著降低青菜地上部分Cu、Zn、Ni和Cd的含量及其氧化性损伤和脂膜损伤(SOD和MDA指标显著降低)。施入钝化剂后,土壤p H显著提高,重金属提取态Cu、Zn、Pb、Ni和Cd普遍降低(硅藻土处理除外)。相关性分析表明,土壤p H与提取态重金属Pb、Zn、Ni和Cd呈显著的负相关,而青菜中的重金属Zn、Ni和Cd的含量与土壤提取态含量呈显著正相关。综合考虑,单一钝化剂牡蛎壳和沸石+牡蛎壳+鸡蛋壳(FMJ)组合对降低青菜重金属吸收的效果尤为显著,可推荐作为重金属复合污染土壤的改良剂。本研究为重金属中轻度污染菜地的土壤修复提供了一种新方法。     

Effect of Olive‐Derived Organic Amendments on Lead,Zinc, and Biochemical Parameters of an Artificially Contaminated Soil

Abstract

An incubation experiment was conducted to ascertain the effects of three olive‐derived organic amendments (fresh, compost, and vermicompost olive cake) on the soluble and diethylenetriamine pentaacetic acid (DTPA)–extractable lead (Pb) and zinc (Zn) and on different enzymatic activities in an artificially contaminated calcareous soil. Application of the compost and vermicompost, which increased amounts of humic acids in soil, initially stimulated dehydrogenase, ß‐glucosidase, and urease activities, which tended to decline afterward. In contrast, dehydrogenase and ß‐glucosidase activities were lower after application of the fresh olive cake. Amounts of soluble Pb and Zn increased when fresh olive cake was added to the soil, due to the high content of water‐soluble carbon in this amendment. On the contrary, application of the compost and vermicompost decreased the concentration of soluble Zn and did not change the soluble Pb levels in the soil. The DTPA‐Pb and DTPA‐Zn were scarcely affected by the application of the three olive‐derived amendments.     

Untersuchungen zur Schwermetalladsorption in einem sauren Waldboden

Investigations of heavy metal adsorption in an acid forest soil To examine the adsorption of heavy metals in an acid forest soil (Pseudogley-Pelosol), undisturbed soil columns of 5 cm length were treated over a period of 276 days with solutions containing Pb, Cu, Zn and Cd. It can be shown that the heavy metals added were preferably adsorbed in the humus-rich, upper part of the soil. When treating the soil with the four heavy metals simultaneously, Pb, Cu and Cd were completely adsorbed in the soil matrix. However 20% of given Zn were leached out of the soil columns. Lowering pH in the percolation solution from pH 4 to 3 led to the mobilisation of previously adsorbed Cu, Cd and Zn, whereas Pb completely remained in the soil.     

工业型城乡交错区农业土壤Cu、Zn、Pb和Cd的空间分布及影响因素研究

在江苏省无锡市工业型城乡交错区，选择8km2区域，采集119个土壤样品，对土壤Cu、Zn、Pb,Cd及其有效态含量的空间分布和影响因素进行探讨。结果表明：该区土壤Cu、Zn、Pb、Cd含量和变异系数都明显增加，土壤有效态重金属含量与相应的全量重金属含量具有显著相关性。土壤Cu、Zn、Cd空间变异主要受到工业影响，但由于该区工业类型的多样性和工厂分布的分散性，Cu、Zn、、Cd空间分布模式并不相同。本区土壤Pb的分布与工厂分布的相关性不大，但随与城市距离增加而降低。公路和土地利用与土壤重金属含量的关系表现不明显。该区工业污染对土壤重金属空间变异的影响可能掩盖了公路和土地利用等的影响，建议在城乡交错区合理安排工业布局以控制土壤受重金属污染的范围。     

Organic and Inorganic Amendments Affect Soil Concentration and Accumulation of Cadmium and Lead in Wheat in Calcareous Alkaline Soils

Irrigation with untreated effluent in periurban agriculture could result in accumulation and bioconcentrations of cadmium (Cd) and lead (Pb). Different amendments were used to investigate their effect on availability, concentration, and uptake of metals by wheat in texturally different soils. Crop was irrigated with water containing Cd and Pb at 20 mg L^?1, thereby adding 260 mg pot^?1 of each metal. Amendments included calcium carbonate at 6 or 12%, gypsum at 50 or 100% of the soil gypsum requirement, farm manure at 7.50 or 15.00 g kg^?1 soil, and a control. Amendments decreased ammonium bicarbonate diethylenetriaminepentaacetic acid (AB-DTPA)–extractable Cd and Pb concentrations and uptake by wheat. Dry matter, concentration, uptake, and extractability of Cd and Pb were greater in sandy loam soil compared with those in sandy clay loam soil irrespective of amendments. Sequential extraction showed that more metals were extracted from the control in all fractions and that predominantly metals were found in the carbonate fraction.     

Mining Impacts on Trace Metal Content of Water,Soil, and Stream Sediments in the Hei River Basin,China

The impacts of mining to watersheds are highly variabledepending on the type of mining, processing of ores, andenvironmental factors. This study examined the Hei River incentral China, for impacts of gold and iron mining onconcentrations of metals in river water, river sediments andstream-channel soils. No production processing of ores occurson-site at either mine. Total metal content and extractablemetals using DTPA were determined. Total concentrations of Cd,Cu, Pb and Zn were high in some stream sediments and soils nearthe mine sites; metal concentrations ranged from 4–24, 11–100,11–380, and 33–1600 μg g^-1 for Cd, Cu, Pb, and Zn,respectively, in soil. Total cadmium was high in all soilsand sediments. Extractable metals were low, with the exceptionof Pb and Cu. At the gold mine, extractable Pb ranged from 8 to33%; extractable Cu ranged from 3 to 21% of total metalconcentration. Chromium and Ni were not above typicalconcentrations in either soils or river sediments. An abundance of carbonates, high river water pH, and high water flow rates all appear to contribute to limiting quantities of metals in the river water. If mining activities are not changed, impacts of mining on downstream metal concentrations in river water should be nominal.     

Evaluation of the BCR sequential extraction for trace elements in European reference volcanic soils

Trace metal behaviour in volcanic ash soils displays distinctive features related to the soils’ large contents of metal‐binding phases and to the rapid release of trace metals from glasses and weatherable minerals. In this work, the BCR (Community Bureau of Reference) sequential extraction scheme (exchangeable + weak acid soluble, reducible, oxidizable, and non‐extractable metal fractions) was applied to selected COST‐622 European reference volcanic soils to determine partitioning of zinc and copper between various solid‐phase constituents, along with the major elements Al, Fe and Mn. The total extracted Al (ΣAl) was strongly correlated with acid ammonium oxalate extractable Al (Al_o) (ΣAl = 0.985Al_o+ 0.11, R²= 0.98), while the total extracted Fe clearly underestimated the amorphous fraction. Large values for the non‐extractable Al fraction were associated with the presence of gibbsite and phyllosilicates. Although the Zn and Cu contents of the soils were generally large, total amounts extracted (the potentially mobilizable fraction) were small, especially for Zn and for soils with crystalline secondary minerals. The fraction of the total Cu which was potentially mobilizable generally exceeded that of Zn. In the potentially mobilizable Cu the oxidizable fraction was generally dominant. Biocycling appears to play an important role in the surface enrichment of potentially mobilizable Zn and Mn. Although further methodological research seems necessary, the BCR sequential extraction appears to be a valuable tool for studies on metal dynamics in soils with andic properties.     

Metal accumulation by bermudagrass grown on four diverse soils amended with secondarily treated sewage effluent

Land treatment is increasingly being utilized as a method of waste disposal for both sewage effluent and sludges. While there has been considerable attention directed toward the fate of metallic constituents of sewage sludges, there have been fewer studies of the fate and mobility of metals appled to soils in sewage effluent. This study was undertaken utilizing secondarily treated sewage effluent amended to contain less than 1 mg l^?1 each of Cd, Cu, Ni, Pb, and Zn. The effluent was applied weekly for a period of 1 yr on large undisturbed monoliths of four diverse soils enclosed in lysimeters and sprigged to common bermudagrass (Cynodon dactylon L.). Soil samples were collected periodically and extracted with DTPA to measure plant available metals. Vegetation was harvested, weighed, subsampled and analyzed for total metal content. Total plant uptake of Cd, Cu, Pb, and Ni during the year was less than 1% of that applied. Vegetative uptake of Zn was as high as 2%. Metal uptake was greatest in the soil with the lowest initial pH. Heavy metal concentrations in plant tissue exhibited a cyclic trend. A similar increasing cyclic trend was evident in the DTPA extractable metals in the surface 0 to 12.5 cm of the treated soils. Decreases in plant and DTPA extractable metals occurred when the soils dried, allowing O₂ to enter. Vegetative concentrations of Cd, Cu, and Ni exceeded normal ranges of 0.2 to 0.8, 4 to 15, and 1.0 mg kg^?1, respectively, for vegetation while Pb and Zn were near normal. Only Cd concentration of vegetation posed a threat to grazing animals.     

Soil metal immobilization and ryegrass uptake of lead, copper and zinc as affected by application of organic materials as soil amendments in a short-term greenhouse trial

Green waste compost, peat, coir and wood bark were applied to metal-contaminated mine waste at the rates of 1%, 10% and 20% on dry weight basis, and perennial ryegrass grown over a period of 6 weeks. Addition of amendments led to increased biomass yield in all soils when compared with the non-amended soil. EDTA extractable Pb, Cu and Zn was significantly reduced in amended soil, while leaf and root metal concentrations were also significantly reduced by the application of amendments, especially at applied rates of 10% and 20%. Coir, green waste compost and wood bark stood out as amendments which were consistent in reducing soil extractable and plant tissue Pb, Cu and Zn; while peat rates above 10% enhanced solubility of Cu and Zn because of a lowering of the soil pH.     

长江三角洲地区土壤盐酸可提取态重金属含量的空间变异特征

以江苏昆山市为典型区,对长三角地区土壤盐酸可提取态重金属含量的结构特征进行分析,得出该区盐酸可提取态重金属的空间分布格局并揭示了引起这种分布格局的成因和污染来源,结果表明：昆山市盐酸可提取态Cd、Cr、Cu、Pb、Zn、Hg属强变异,Ni和Co为中等变异。半方差函数模型拟合表明所有盐酸可提取态重金属元素均符合球状模型,8种重金属元素在一定范围内均存在空间相关性。采用Kriging最优内插法得到了盐酸可提取态重金属含量的空间分布格局,表明土壤盐酸可提取态重金属含量与工业活动、污水灌溉和大气降尘密切相关。通过主成分分析与地统计学相结合的方法,得出该区盐酸可提取态重金属由4个主成分构成,第一主成分为Cd、Cu、Pb、Cr和Zn,决定这一成分的主要因素为工业污水灌溉、大气降尘和元素地球化学特征;第二主成分为Ni,决定这一成分的主要因素为土壤内部因子;第三主成分为Hg,该成分主要受工业点源污染的影响;第四主成分为Co,该成分可能主要受地形影响。     

Residual heavy metal concentrations in sludge‐amended coastal plain soils ‐ I. Comparison of extractants

Abstract

The purposes for this research were: to examine the long‐term residual effects of farmland applications of municipal sludges from four treatment technologies on the total and extractable Zn, Cu, Mn, Fe, Pb, Ni and Cd concentrations in Coastal Plain soils; to investigate the effects of sludge sources and rates on the effectiveness of soil extractants to remove the various metals; and to determine correlation coefficients for soil extractable versus plant accumulation in tobacco. The extractants evaluated were Mehlich 1 and 3, and DTPA‐pH 7.3. Composite Ap horizon soil samples and tobacco leaf samples were obtained in 1984 from research plots at two sites in Maryland that were established in 1972 and 1976, respectively, using sludge materials from three wastewater treatment facilities in the Washington, D.C. metropolitan region. Similar application rates were used at both sites.

A wide range in soil pH values was found among treatments at each site. Significant (p ≤ 0.05) increases were observed in total Zn, Cu, Fe, Pb, Ni, and Cd for all sludge sources with increased rates; however, values for total soil Mn exhibited high variability in all cases. The rankings among the extractants varied for some elements depending on the sludge sources. For Zn, the rankings were Mehlich 1 > Mechlich 3 > DTPA‐pH 7.3 across all sources and rates. For Cu, Mehlich 3 > Mehlich 1 > DTPA‐pH 7.3 was found for soils amended with Blue Plains digested (BPD) and Piscataway limeddigested (PLD) sludges but Mehlich 1 ≥ DTPA pH 7.3 > Mehlich 3 for Blue Plains limed compost (BPLC) and Annapolis Fe and heat treated (AFH) sludges. Concerning extractable Mn, Mehlich Mehlich 1 > Mechlich 3 > DTPH pH 7.3 was the order for BPLC and AFH sludges but Mehlich 3 > Mehlich 1 > DTPA‐pH 7.3 was observed for BPD and PLD sludges. The rankings among extractants for Fe (Mehlich 3 > Mehlich 1 > DTPA‐pH7.3), Ni (Mehlich 3 ≥ Mehlich 1 > DTPA‐pH 7.3), Pb (Mehlich 3 > DTPA‐pH 7.3 > Mehlich 1) and Cd (Mehlich 1 > Mehlich 3 > DPTA‐pH7.3) were somewhat similar across all sludge sources. Significant correlation coefficients were obtained for all three extractants for soil extractable vs. plant Zn, Cu, Ni, and Cd at both sites; however, Mehlich 3 was not significant for Mn. Also, neither of the extractants produced significant coefficients for Fe and Pb.