Toxicity of heavy metals (Zn,Cu, Cd,Pb) to vascular plants

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

Temporal Patterns of the Wet Deposition of Zn,Cu, Ni,Cd and Pb: The Arcachon Lagoon (France)

We report here the first data set on wet deposition of heavy metals in the southwestern French coastal zone. In this region, there are two major sensitive coastal ecosystems: the Gironde Estuary and the Arcachon Lagoon. Chemical analyses of heavy metals were carried out by ICP-MS. Annual mean concentrations of the dissolved fraction in precipitation were 0.2, 3.4, 4.3, 8.1 and 30 μg L^-1for Cd, Ni, Cu, Pb and Zn, respectively. In terms of annual fluxes, these numbers are of the same order of magnitude as the fluxes measured in southeastern France, but are higher than those measured in western Brittany. When extrapolated to the entire Bay of Biscay, the annual wet dissolved fluxes of Cd, Ni, Cu, Pb and Zn are respectively 7, 110, 140 340 and 1440 t yr^-1. According to available data in the literature, the regional Cd, Cu, Pb and Zn atmospheric fluxes for the Bay of Biscay are of the same order of magnitude as riverine inputs (Loire and Gironde). On a daily or weekly time scale, we observed a strong variability of elemental fluxes: up to 20% of the annual dissolved flux may occur in a rain event shorter than 3.5 days. Although elements display generally parallel variations with time, they sometimes follow independent behaviours (e.g. Pb and Cd), suggesting that they may derive from different geographical and/or pollution sources.     

Fluxes of Cu,Zn, Pb,Cd, Cr,and Ni in temperate forest ecosystems

The literature on the fluxes of six heavy metals in temperate forest ecosystems is reviewed. Special attention is given to wet and dry deposition and internal flux, to metal budgets for ecosystems and soils, to concentrations in aqueous compartments of the ecosystem and to speciation in soil solutions. Metal fluxes are discussed in relation to pollution load, soil type, tree species and land use. The mobility of Cu and Pb is strongly dependent on the solubility of organic matter. These metals are commonly accumulated in forest soils. Zinc, Cd and Ni are greatly influenced by soil acidity and are often lost in considerable amounts from acidified soils. Chromium is often at balance in forest ecosystems. Implications for metal solubility and budgets in forest soils are discussed in connection with an increase in soil acidification.     

Solubility control of Cu, Zn, Cd and Pb in contaminated soils

We developed a semiempirical equation from metal complextion theory which relates the metal activity of soil solutions to the soil's pH, organic matter content (OM) and total metal content (MT). The equation has the general form: where pM is the negative logarithm (to base 10) of the metal activity, and a, b and c are constants. The equation successfully predicted free Cu²⁺ activity in soils with a wide range of properties, including soils previously treated with sewage sludge. The significant correlation of pCu to these measured soil properties in long-contaminated soils suggests that copper activity is controlled by adsorption on organic matter under steady state conditions. An attempt was made from separate published data to correlate total soluble Cu, Zn, Cd and Pb in soils to soil pH, organic matter content and total metal content. For Cu, the total Cu content of the soil was most highly correlated with total soluble Cu. Similarly, total soluble Zn and Cd were correlated with total metal content, but were more strongly related to soil pH than was soluble Cu. Smaller metal solubility in response to higher soil pH was most marked for Zn and Cd, metals that tend not to complex strongly with soluble organics. The organic matter content was often, but not always, a statistically significant variable in predicting metal solubility from soil properties. The solubility of Pb was less satisfactorily predicted from measured soil properties than solubility of the other metals. It seems that for Cu at least, solid organic matter limits free metal activity, whilst dissolved organic matter promotes metal solubility, in soils well-aged with respect to the metal pollutant. Although total metal content alone is not generally a good predictor of metal solubility or activity, it assumes great importance when comparing metal solubility in soils having similar pH and organic matter content.     

Partitioning of metals (Cd, Co, Cu, Ni, Pb, Zn) in soils: concepts, methodologies, prediction and applications – a review

Prediction of the fate of metals in soil requires knowledge of their solid–liquid partitioning. This paper reviews analytical methods and models for measuring or predicting the solid–liquid partitioning of metals in aerobic soils, and collates experimental data. The partitioning is often expressed with an empirical distribution coefficient or K_d, which gives the ratio of the concentration in the solid phase to that in the solution phase. The K_d value of a metal reflects the net effect of various reactions in the solid and liquid phases and varies by orders of magnitude among soils. The K_d value can be derived from the solid–liquid distribution of added metal or that of the soil‐borne metal. Only part of the solid‐phase metal is rapidly exchangeable with the solution phase. Various methods have been developed to quantify this ‘labile’ phase, and K_d values based on this phase often correlate better with soil properties than K_d values based on total concentration, and are more appropriate to express metal ion buffering in solute transport models. The in situ soil solution is the preferred solution phase for K_d determinations. Alternatively, water or dilute‐salt extracts can be used, but these may underestimate in situ concentrations of dissolved metals because of dilution of metal‐complexing ligands such as dissolved organic matter. Multi‐surface models and empirical models have been proposed to predict metal partitioning from soil properties. Though soil pH is the most important soil property determining the retention of the free metal ion, K_d values based on total dissolved metal in solution may show little pH dependence for metal ions that have strong affinity for dissolved organic matter. The K_d coefficient is used as an equilibrium constant in risk assessment models. However, slow dissociation of metal complexes in solution and slow exchange of metals between labile and non‐labile pools in the solid phase may invalidate this equilibrium assumption.     

Changes in Cd,Cu, Ni,Pb and Zn Fractionation and Liberation Due to Mussel Shell Amendment on a Mine Soil

Mining activities are related to relevant environmental pollution issues that should be controlled. We used sequential extractions to fractionate Cd, Cu, Ni, Pb and Zn retained on unamended or mussel shell‐amended mine soil samples, all of them treated with a mixture of the five heavy metals (total metal concentration of 1·57 mmol L⁻¹), after 1, 7 and 30 days of incubation. In addition, we used the stirred flow chamber technique to study the release of each of the five heavy metals from these different unamended and shell‐amended soil samples. The results indicate that the shell amendment caused a decrease in the most soluble fraction, while increasing the most recalcitrant (least mobile) fraction. With equivalent implications, the stirred flow chamber experiments showed that mussel shell amendment was associated to a decrease in heavy metal release and increased retention. The highest mussel shell dose and incubation time caused the most relevant changes in pH values and thus in metal retention, also indicating the importance of pH modifications in the mechanism of retention acting in the amended samples. In view of these results, the use of mussel shell amendment can be encouraged to increase heavy metal retention in acid mine soils, in order to minimise risks of environmental pollution. Copyright © 2016 John Wiley & Sons, Ltd.     

Simultaneous Sorption of Cd,Cu, Ni,Zn, Pb,and Cr on Soils Treated with Sewage Sludge Supernatant

Disposal of sewage sludge creates the potential for heavy metal accumulation in theenvironment. This study assessed nine soils currently used as Dedicated Land Disposal units(DLDs) for treatment and disposal of municipal sewage sludge in the vicinity of Sacramento,California. Adsorption characteristics of these soils for Cd, Cu, Ni, Zn, Pb, and Cr were studiedby simultaneously mixing these elements in the range of 0-50 µmol L-1 with sludgesupernatant and reacting with the soil using a soil:supernatant ratio of 1:30, pH = 4.5 or 6.5, andconstant ionic strength (0.01 M Na-acetate). The concentration of metals in the supernatant wasdetermined after a 24 hr equilibration period. Adsorption isotherms showed that metal sorptionwas linearly related to its concentration in the supernatant solution. The distribution coefficientKd (Kd = concentration on solid phase/concentration in solution phase) was computed as theslope of the sorption isotherm. The distribution coefficients were significantly correlated to soilorganic matter content for Ni, Cu, Cd, and Pb at pH 4.5 and for Ni, Cu, Zn, and Cd at pH 6.5.There was also a correlation between Kd and soil specific surface area but no relationship to othersoil properties such as CEC, clay content, and noncrystalline Fe and Al materials. Therefore, soilorganic carbon and surface area appear to be the most important soil properties influencing metaladsorption through formation of organo-metal complexes. The Kd values for all elements werehigher at pH 6.5 than at 4.5. Selectivity between metals resulted in the following metal affinitiesbased on their Kd values: Pb>Cu>Zn>Ni>Cd≈Cr at pH 4.5 andPb>Cu≈Zn>Cd>Ni>Cr at pH 6.5.     

The flux of Cd,Cu, Pb and Zn in mining polluted soils

The monitoring of heavy metal deposition onto soils surrounding old Pb-Zn mines in two locations in the UK has shown that relatively large amounts of Cd, Pb, Zn and, in one case, Cu are entering the soil annually. Small particles of ore minerals in windblown mine tailings were found to be contributing up to 1.46 g m^?2 yr^?1 of Pb, 1.41 g m^?2 yr^?1 of Zn and 0.027 g m^?2 yr^?1 of Cd. However, when these inputs from bulk deposition are compared with the concentrations of the same metals within the soil profiles it is apparent that relatively little long-term accumulation is occurring. Metals are being lost from the soil profiles, probably through leaching. A calculated relative retention parameter gave values that ranged from 0.01 to 0.17 for Cd, 0.11 to 0.19 for Zn, 0.32 to 0.63 for Cu and over 1 for Pb. These relative retention values were found to follow the order of electronegativity of the elements concerned: Pb>Cu>Zn>Cd. Distribution coefficient (Kd) values quantifying the adsorptive capacity of the mine soils for Cd and Pb showed marked differences for the two metals (12 to 69 cm³ g^?1 for Cd and 14 to 126 cm³ g^?1 for Pb) and may, in part, account for the two to one hundred-fold variation in the relative retention parameter for the different metals within these soils.     

Competition from Cu(II), Zn(II) and Cd(II) in Pb(II) Binding to Suwannee River Fulvic Acid

This is a study of trace metal competition in the complexation of Pb(II) by well-characterized humic substances, namely Suwannee River Fulvic Acid (SRFA) in model solutions. It was found that Cu(II) seems to compete with Pb(II) for strong binding sites of SRFA when present at the same concentration as Pb(II). However, Cd(II) and Zn(II) did not seem to compete with Pb(II) for strong binding sites of SRFA. These two metals did compete with Pb(II) for the weaker binding sites of SRFA. Heterogeneity of SRFA was found to play a crucial role in metal–SRFA interactions. The environmental significance of this research for freshwater is that even at relatively low Pb(II) loadings, the metals associated with lead in minerals, e.g. Cu(II), may successfully compete with Pb(II) for the same binding sites of the naturally occurring organic complexants, with the result that some of the Pb(II) may exist as free Pb²⁺ ions, which has been reported to be one of the toxic forms of Pb in aquatic environment.     

Role of soil constituents in fixation of soluble Zn, Cu, Ni and Cd added to soils

Slow immobilization of trace metals in soil, termed ‘fixation’, affects their natural attenuation but it is still unclear which reactions occur. Twenty‐eight soils were selected to assess the role of Fe oxides and carbonates on fixation of Cu, Cd, Zn and Ni. Soils included samples from 2 toposequences (Vietnam, Spain) and 13 European topsoils with different soil characteristics (pH 3.4–7.7). Samples were amended with 250 mg Zn kg⁻¹, 100 mg Cu kg⁻¹, 80 mg Ni kg⁻¹ and 2.5 mg Cd kg⁻¹ as metal salts and incubated for 850 days. Fixation was measured as the increase of the fraction of added metals that were not isotopically exchangeable. Fixation increased with time and was, averaged over all the soils, 43% (Cu), 41% (Zn), 41% (Ni) and 28% (Cd) after 850 days. Metal fixation within samples from each toposequence was generally positively related to total Fe oxide concentration (Fe_d) for Zn, Ni and Cd. However, the fixation of Cd, Zn and Ni was mainly explained by pH and not by Fe_d when considering all soils. Fixation of Zn and Cd in soils with pH >7.0 increased with increasing concentrations of carbonates at initial ageing times. Fixed fractions of Zn, Ni and Cd were significantly released when experimentally removing 50% of carbonates by acidification. Fixation of Cu was most poorly related to soil properties. Our data suggest that fixation of Cd, Zn and Ni is related to a pH‐dependent diffusion into oxides and that of Cd and Zn also to diffusion and/or coprecipitation in carbonates. Fixation of Ni at neutral pH may also be related to stabilization of precipitates that form readily in soil.     

Changes in Concentrations of Cd,Zn, Mn,Cu and Pb in Spruce (Picea abies) Needle Litter During Decomposition

Spruce (Picea abies (L.) Karst) needle litter was placedin litterbags and incubated (≥6 yr) at five spruce standsin southern Sweden. The litterbags were collected twice a yearduring year 1–2 and thereafter once a year, for total analyses(conc. HNO₃) of Cd, Zn, Mn, Cu and Pb. The main objectiveswere to document changes in concentrations and amounts of theseelements during litter decomposition and to investigate factorscontrolling the changes.Concentrations of Cd, Zn, Cu and Pb increased to at least 0.5, 1.5, 3 and 13 times the initial concentration. During the latterpart of the incubations, concentrations became more stable ordecreased. Concentrations at which the metals are considered to be toxic to micro-organisms in the mor layer were not reached during the experiment. Generally, concentrations of Mn decreased.Total amounts of Cd, Zn and Mn had decreased by at least15, 24 and 43%, from the initial amount at the end of theexperiment. The total amount of Cu increased (>40%) before itstarted to decrease. The total amount of Pb increased by over230%. Thereafter it became more constant or decreased.According to a PCA, the dynamics of total amounts of Cd,Zn and Mn in the litter were similar, as were those of Pb and Cu.Furthermore, in most cases the heavy metal amounts on anysampling occasion differed more between than within sites. Thedynamics of total amounts of elements were more similar betweenadjacent sites than between more distant sites.     

Modelling of Cd, Cu, Ni, Pb and Zn uptake, by winter wheat and forage maize, from a sewage disposal farm

Abstract. A predictive model of metal concentrations in crops was developed to optimize soil liming and sludge application strategies at a dedicated sewage sludge disposal site. Predictions of metal concentrations in plant tissue were derived from measured values of soil metal concentration, humus content and soil pH. The plant and soil data used to parameterize the model were collected on site using quadrat sampling of mature crop and underlying topsoil. The uptake model was used to map predicted metal concentrations in wheat grain and forage maize based upon a database of soil characteristics (metal content, % humus and pH) measured as part of a routine geochemical survey of the site. The effect of a management strategy to modify uptake of Cd by wheat by changing soil pH was investigated. The effect of soil dust adhering to maize plants at harvest was also simulated to investigate the importance of this pathway for Cd transfer to animal feed such as silage.
The model gave satisfactory predictions for uptake of Cd and Zn but less useful simulations for Pb, Cu and Ni. The results for Cd uptake showed a greater dependence on soil pH in the case of wheat in comparison to maize. It is suggested that, for the study site, liming to pH 7.0 will reduce Cd concentrations in wheat grain to within EC legal standards. However the Cd content of maize may still exceed these guidelines, with a relatively minor contribution from contamination with soil dust.     

Chemical speciation and bioavailability of Cd,Cu, Pb and Zn in Western Balkan soils

Abstract

Three thermal power plants in Serbia, Croatia and Bosnia of the Western Balkan region were expected to be metal polluting sources, and this study was performed to investigate the bioavailability and chemical speciation of trace metals in soils and soil water extracts, respectively. Surface (0–15 cm) soil samples along with maize and grass samples were collected at a gradient from the pollution source. The chemical speciation of metals was conducted using the Windereme Humic Aqueous Model (WHAM)/Model VI for water, whereas the Diffusion Gradient in Thin Films (DGT) technique was used to estimate plant availability. The chemical speciation indicated that more than 99% of all four metals in soil water extracts were complexed to fulvic acid. This is connected to relatively high soil pH (> 6.5) and high contents of soil organic matter in these soils. The accumulation of trace metals by DGT was not correlated to plant uptake. This is connected to the very low partitioning of free ions in solution, but also to the low variation in metal solubility and metal concentration in plant tissue between sites. In spite of active thermal power plants located in the areas, hardly any differences in concentration of soil metals between sites were seen and the partition of metals in soil waters was insignificant. The latter indicates that these soils have a large metal-retaining capacity. The only significant soil chemical variable affecting the variation in metal solubility was the soil pH. In a time with large infrastructure and industrial expansion in these areas, this investigation indicates the importance of protecting these high-quality soils from industrial use and degradation. High industrial activity has so far had insignificant effect on soil quality with respect to bioavailability of trace metals in these soils.     

洞庭湖区典型蔬菜土壤镉、铜、锌、铅含量状况及评价

采用单项污染指数和综合污染指数法对湖南洞庭湖区典型蔬菜土壤Cd,Cu,Zn,Pb含量状况进行了评价。结果表明,与湖南省潮土土壤背景值相比,土壤Cd,Cu和Zn含量明显富集,Pb含量总体不高。与国家土壤质量二级标准(GB15618-1995)相比,洞庭湖区蔬菜土壤以Cd污染为主,其次是Zn和Cu。Pb含量没有超标,其中湘阴县、沅江市、资阳区和赫山区蔬菜土壤环境质量为轻度污染,华容县处于警戒水平,需要修复治理或者改变土地利用方式。君山区和南县蔬菜土壤为清洁水平,适宜发展无公害蔬菜。污染风险高的区域土壤Cd,Cu和Zn之间存在极显著或显著正相关关系,但相关性弱。     

Retention of Cd, Cu, Pb and Zn by Wood Ash, Lime and Fume Dust

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

Zn、Cu、Pb、Cr、Cd对鲫肌动球蛋白和肌球蛋白加工特性的影响

为了解重金属离子污染对鱼体质地的影响,通过外源添加不同浓度的Zn(Ⅱ)、Cu(Ⅱ)、Pb(Ⅱ)、Cr(Ⅲ)、Cd(Ⅱ)重金属离子,采用质构仪测定添加不同浓度金属离子对肌动球蛋白和肌球蛋白黏性和凝胶特性的影响。结果表明,肌动球蛋白和肌球蛋白溶液的硬度、稠度、黏度、黏聚性受离子浓度影响,硬度和稠度先下降后升高,黏性和黏聚性先略有升高,而后出现下降的趋势,Zn(Ⅱ)、Cr(Ⅲ)、Cd(Ⅱ)引起的变化显著(p＜0.01)。金属离子浓度增加对鱼蛋白凝胶的硬度、黏聚性、胶黏性、咀嚼性有显著影响(p＜0.01),降低鱼蛋白食用价值。     

Changes in organic carbon and nitrogen in soil with metal pollution by Cd,Cu, Pb and Zn: a meta‐analysis

Organic carbon (OC) and nitrogen (N) storage in soil plays an important role in global climate change and in maintaining food security. Pollution of soil with heavy metals has occurred in many parts of the world, but their effects on soil OC and N have not been well addressed. Relevant data were extracted from peer‐reviewed journal papers and analysed by a meta‐analysis to determine how long‐term heavy metal pollution affected soil OC and N status. Plant biomass decreased significantly because heavy metals in soil decreased soil OC and N concentrations by 5.0 and 17.9%, respectively, but increased the C/N ratio by 5.1%. The largest reductions in soil OC and N concentrations were in soil more strongly polluted by metals. The changes in soil OC and N with metal pollution varied with climatic conditions. More substantial decreases in OC and N concentrations were likely to occur in polluted soil with large background contents of OC and low pH. Overall, heavy metals were linked to greater reductions in soil OC and N concentrations in natural ecosystems than in agro‐ecosystems. These results provided a quantitative evaluation of the effects of heavy metal pollution on the decrease in soil C and N concentrations and, therefore, on global climate change. Further consideration should be given to changes in the cycling of C and N in soil polluted with metals in natural and agro‐ecosystems.     

Heavy metal accumulations of 24 asparagus bean cultivars grown in soil contaminated with Cd alone and with multiple metals (Cd, Pb, and Zn)

Crops grown in heavy metal contaminated soils are an important avenue for these toxic pollutants entering the human food chain. Information on how crops respond to soil contaminations of single versus multiple metals is scarce and much needed. This study investigated the accumulation of Cd by 24 cultivars of asparagus bean (Vigna unguiculata subsp. Sesquipedalis L., family Fabaceae) under a low level (0.8 mg kg-1) and a high level (11.8 mg kg-1) of Cd exposure in a garden experiment, and that in a field experiment with Cd, Pb, and Zn (1.2, 486, and 1114 mg kg-1, respectively) contaminated soil. Both experiments showed that there were highly significant variations among the tested cultivars in Cd accumulation by roots, stems, leaves, and fruits of asparagus bean. In the garden experiment, all cultivars under the low Cd exposure and 41.7% of the tested cultivars under the high Cd exposure bore fruits (pods) whose Cd concentrations were lower than 0.05 mg kg-1 fw and therefore were safe for consumption. In addition, the fruit Cd concentrations of cultivars with black seed coats were significantly lower than those with red or spotted seed coats. These results suggest that asparagus bean is a hypo-accumulator to Cd pollutant and the trait of Cd accumulation is genetic-dependent among cultivars. In the field experiment, correlation between fruit Cd and Pb concentrations was significantly positive (p < 0.05). Additional correlation analyses between two experiments showed that fruit Cd concentrations in the field experiment were significantly correlated with those exposed to the high level of Cd stress, instead of to the low level of Cd stress in the garden experiment. This suggests that the presence of other toxic heavy metals in the soil might have facilitated the accumulation of Cd in fruits, and the selection of pollution-safe-cultivars (PSC) in multi-metal polluted condition could refer to the PSCs selected under a high level exposure of a single heavy metal.     

绿化植物废弃物对重金属迁移的影响

采用土柱模拟实验,比较研究了覆盖绿化植物废弃物与土壤之上和绿化植物废弃物与土壤混合处理对城市绿地土壤中重金属淋溶的影响。结果表明,Zn、Pb和Cd均在80天后淋溶完全,而Cu有所不同,在80天后又有增加的趋势,原因可能跟重金属与有机质的结合能力有关。此外,绿化植物废弃物与土壤相混合能抑制Cu、Zn、Pb和Cd向下淋溶,而绿化植物废弃物覆盖于土壤之上则有促进Cu、Zn、Pb和Cd淋溶的趋势,且不论是混合处理还是覆盖处理,20cm厚绿化植物废弃物的处理均比10cm厚绿化植物废弃物处理对Cu、Zn、Pb和Cd的促进或抑制作用大。研究还得知,Cu、Zn、Pb和Cd的迁移还与土壤pH有关,低pH土壤有利于重金属的淋溶。     

Distribution of Zn, Cd, Pb and Cu Metals in Groundwater of the Guadiamar River Basin

Traditionally, the Guadiamar River Basin (Seville, SouthwestSpain) has received pollution from two different sources. Inits upper course, from a pyrite exploitation and, in itslower reaches, from untreated urban and industrial wastes aswell as wastes from intensive agricultural activity. In 1998,the accidental release in the river of about 6 million m³ of acid water and sludge from mine tailings contributedto worsen the pollution of an already contaminated area. Themain polluting agents of the spill were heavy metals. Itaffected a large number of wells either directly or as a consequence of infiltration from polluted soils. Assessment of the pollution by total metal determination does not revealthe true environmental impact of the spill and speciation studies showing the distribution of the main pollutants are required. There is a direct association between the physicochemical speciation of an element and its bioavailability, toxicity and mobility. This article describesa distribution study of the metals Zn, Cd, Pb and Cu by speciation analysis of groundwater in six wells of the GuadiamarRiver Basin; the samples were taken several weeks after the spill. The speciation analysis resulted in the definition ofthree species categories: a) labile metal (H⁺ exchangeable),b) metal strongly associated to dissolved organic matter and c) metal associated with suspended material. Analysis was carried out by anodic stripping voltammetry (ASV). Metal speciation ingroundwater of the Guadiamar River Basin allows a differentiationbetween: on the one hand, metals from the mining spill, andon the other hand a less recent pollution from accumulatedinfiltration of either mining or agricultural origin, the last one due to an abuse of phytosanitary products.