Sequential extraction and speciation of Ba,Cu, Ni,Pb and Zn in soil contaminated with automotive industry waste

Abstract

Sequential extraction or fractionation of heavy metals in the solid phase and their speciation in soil solution are important tools for assessing changes resulting from land use and/or pollution. The distribution of the various forms of Ba, Cu, Ni, Pb and Zn was evaluated in soil samples taken from a polluted area, and the speciation of cations and anions in a soil solution contaminated with automotive industry waste. We evaluated the sequential extraction and speciation of Ba, Cu, Ni, Pb and Zn in a Leptosol associated with a Cambisol and contaminated with automotive industry waste. Soil samples were collected at 0-0.2 m (a mix of soil and waste); 0.2-0.4 m (waste only), and 0.4-0.6 m (soil only) both in the polluted area and in two contiguous unpolluted areas: a sugarcane plantation and a forest fragment. Total concentrations of metals in the polluted area were above limits for intervention established by European Community regulations. Cu was mostly distributed in the residual and in the oxide-bonded fractions, except for the waste-only sample, in which the carbonate-bonded fraction was significant. Zn was concentrated in the residual and carbonate-bonded fractions, while Ba, Ni and Pb predominated in the residual fraction of the contaminated samples. Metals in the soil solution were predominantly in the hydroxyl forms, except for Ba, which was mostly in the ionic form (Ba²⁺).     

Phytoremediation efficiency of Eichhornia crassipes in fly ash pond

The present study was focused on field research to examine the phytoremediation potential of naturally grown Eichhornia crassipes in fly ash (FA) pond. Field results indicate the efficiency of E. crassipes for remediation of heavy metals from FA pond. The bioconcentration factor trend was Cr (3.75) > Cu (2.62) > Cd (1.05), and Cu (1.35) in root and stem, respectively. The survival and abundance growth of E. crassipes in the circumstance of heavy metal enriched FA pond is another highlight of the present research that reveals its toxitolerant characteristics. Thus, this lesson on phytoremediation proved that E. crassipes is a potential accumulator of Cu, Cr, and Cd from FA ponds and is a promising species for FA pond's remediation globally.     

绿洲土Cd、Pb、Zn、Ni复合污染下重金属的形态特征和生物有效性

通过模拟基于干旱区绿洲土壤Cd-Pb-Zn-Ni复合污染下的油菜盆栽试验,采用Tessier五步连续浸提法探究了重金属复合污染对油菜生长的影响及其各形态的转化归趋和生物有效性.结果显示,随着Cd-Pb-Zn-Ni复合胁迫水平的升高,油菜的干重先增加后减小,根系的生长由促进作用转变为抑制作用;对照土壤中4种重金属元素均以残渣态为主要赋存形态,可交换态的含量均很小;随着外源重金属的添加,油菜种植土壤中4种重金属元素的各形态含量随之增加,Cd、Pb、Zn的可交换态和Ni的碳酸盐结合态对外界胁迫响应强度最大,Cd、Pb、Zn、Ni的活性增加,且Cd、Pb的主要赋存形态迅速转变为碳酸盐结合态和铁锰氧化态,Zn的主要赋存形态由残渣态和碳酸盐结合态过渡到碳酸盐结合态和铁锰氧化态,Ni的主要赋存形态为碳酸盐结合态;Cd、Zn在茎叶中的含量大于根系,Pb、Ni反之,油菜能将Cd、Zn更多的运输至茎叶,Pb、Ni则主要积累在根系;油菜茎叶吸收Cd和油菜各部位吸收Zn的主要贡献形态为可交换态,根吸收Cd的主要贡献形态由可交换态转变为有机结合态,根吸收Pb和油菜各部位吸收Ni的主要贡献形态为碳酸盐结合态.     

Sludge-Derived Cu and Zn in a Humic-Gley Soil: Effect of Dissolved Metal-Organic Matter Complexes on Sorption and Partitioning

A sequential extraction scheme was combined with sorption isotherm analysis in order to investigate sorption of sewage sludge-derived Cu and Zn to the A-horizon of a humic-gley soil as a whole, and to the operationally defined exchangeable (1?M MgCl₂), carbonate (1?M NaOAc), Fe/Mn oxide (0.04?M NH₂OH.HCl), and organic (0.02?M HNO₃+30% H₂O₂) soil fractions. Sorption parameters were compared for a sample of sludge leachate (with 97.4% of Cu and 63.2% of Zn present as dissolved metal-organic matter complexes, as calculated by geochemical modeling involving MINTEQA2 and verified using an ion exchange resin method) with that of a reference solution exhibiting the same chemical characteristics as the leachate, except for the presence of dissolved organic material. Dissolved metal-organic matter complexes were found to significantly (P<0.05) depress sorption to the bulk soil and each fraction. The greatest depression of Cu and Zn sorption was observed for the exchangeable, carbonate, and Fe/Mn oxide fractions, while the organic fraction of the soil was the least affected. This reflects a greater affinity for the exchangeable, carbonate, and Fe/Mn oxide fractions by the free divalent metal (Cu²⁺, Zn²⁺), with sorption by these fractions attributed to cation exchange, chemisorption, and co-precipitation processes. The sorption characteristics of the organic fraction indicated that Cu and Zn sorption by soil organic matter mostly involved dissolved metal-organic matter complexes. This may be attributed to hydrophobic interactions between nonpolar regions of the dissolved metal-organic matter complexes and solid-phase soil organic matter.     

Chemical partitioning of Cu,Pb and Zn in the soil profile of a semi arid dry woodland

Abstract

The chemical partitioning of Cu, Pb and Zn was examined in the soil profile of the woodland system in Keoladeo National Park, India using a five-step sequential extraction procedure (SEP). Metal partitioning was assessed in the soil up to a depth of 100cm with 25-cm intervals. The amount of metals obtained from the SEP exceeded pseudototal metal levels obtained from aqua regia digestion. The SEP results showed high preferential attachment of metals with Fe—Mn hydroxides. All the three metals showed least preferences to the exchangeable pool. The attachment of metals to the OM-S phase was also less, may be because of the low organic matter in the soil. In the case of Cu, the order of the fractions in terms of metal concentrations was Fe—Mn>RES>OM-S>CA>EXC and in the case of Pb the order was Fe—Mn>OM-S>RES>CA>EXC. Zn was different from Cu and Pb in showing higher affinity towards RES phase and the order of its concentration was RES>Fe—Mn>OM-S>EXC>CA. This suggests hydrous oxides of Fe—Mn as an important binding site for Cu and Pb, whereas silicate mineral matrix (RES phase) for Zn.     

Partitioning of Zn,Cd, Pb,and Cu in organic-rich soil profiles in the vicinity of a zinc smelter

Abstract

A five-step sequential extraction procedure was applied to organic-rich soil samples from five soil profiles situated 1–8 km from a zinc smelter. The partitioning of Zn, Cd, Pb, and Cu into five operationally defined fractions (exchangeable, “carbonate’’-bound, reducible, oxidizable, and residual) was studied at different soil depths down to 35cm. In the surface soil (0–1 cm) a major part of Pb and Cu was extracted in the oxidizable fraction, whereas for Zn and Cd slightly more was extracted in the ‘‘carbonate”-fraction than in the other four fractions. Extracted metal proportions in the oxidizable fraction were respectively of the order of 30%, 20%, 50%, and 80% for Zn, Cd, Pb, and Cu in the surface soil for all sites, but these proportions decreased with soil depth. In the surface soil less than 20% of all the elements were extracted in the residual fraction, but the proportions associated with this fraction generally increased with soil depth. In the C-horizon, differences in extracted proportions of Pb and Cu in the residual fraction were probably due to geochemical factors, whereas for Zn the low extracted proportion at a highly contaminated site (20%) may be due to Zn migration to the C-horizon at this site. For Cd the extracted proportions in the C-horizon were lower than for the other elements, generally below 20%, presumably because Cd is weaker in terms of its adsorption to the soil than the other elements studied. Total concentrations of the metals decreased strongly with increasing distance from the smelter, but less systematic differences were observed for their distributions among fractions. Potentially bioavailable metal proportions (exchangeable + “carbonate”-bound fraction) in the surface soil were about 50%, 60%, 20%, and 10% for Zn, Cd, Pb, and Cu, respectively. In C-horizon soil the mobility sequence Cd>Zn>Pb = Cu was generally observed. The present results indicate that the concentrations and chemical fractionation of Zn, Pb, and Cd in these soils represent a considerable risk to natural terrestrial food chains.     

Risk Element (As,Cd, Cu,Pb, and Zn) Contamination of Soils and Edible Vegetables in the Vicinity of Guixi Smelter,South China

Risk element (As, Cd, Cu, Pb, and Zn) contamination in soils and in two edible vegetables (Solanum melongena L. and Capsicum annum L.) was investigated in the vicinity of Guixi Smelter, South China. Soil As concentrations averaged 23.9 mg/kg. Sites near the smelter tailings recorded the highest levels of As and heavy metals in soils. The concentration order of heavy metals in soils was Cd < Pb < Zn < Cu. Cu and Cd in soils were abundant in the exchangeable and bound to carbonate fraction, while Pb and Zn were in the residual fraction, limiting their potential toxicity as pollutants. The proportions of the metals in the mobile fraction followed the order Pb < Zn < Cu < Cd. In Solanum melongena L. and Capsicum annum L., Zn concentration was the highest, followed by Cu, Cd, and Pb, different from that in soils and in the mobile fraction. Concentrations of heavy metals in the labile fractions in soils and in vegetables presented significant correlation (p < 0.05). Both of the two vegetables are not the Cu and Zn accumulators. As for Cd and As, Capsicum annum L. poses a higher risk to animal and human health than Solanum melongena L., with soil-plant transfer coefficients more than three. Root-stem is the main barrier for most of the heavy metals and As in the two vegetables, resulting in higher metal concentrations in roots relative to other plant tissues. The low stem-fruit transfer coefficients for Zn in Solanum melongena L. and for Pb in Capsicum annum L. suggested that very few of them could reach the fruits.     

Leachant pH effects on the leachability of metals from fly ash

The leachability of metals from fly ash produced by a coal‐fired electric plant and a municipal waste incinerator under acidic conditions was experimentally investigated. The results of these column‐leaching experiments show that a decrease in the pH of the leachant favors the extraction of metal ions from solid particles of both coal combustion fly ash and municipal waste incinerator fly ash. The significant increase in the extraction of cadmium, chromium, zinc, lead, mercury, and silver ions from the ash is attributed to the instability of the mineral phases that contain these metals under acidic conditions.     

Distribution,Speciation and Bioaccumulation of Hg and As in Mariculture Sediments from Dongshan Bay,China

Hg and As are the major hazardous pollutants in marine sediments due to their high toxicity to benthonic organisms. Understanding the spatial distribution, speciation and bioaccumulation of these toxic elements in sediments is therefore of high environmental importance for identifying their potential risks. Sediments and bivalves Paphia undulata were collected from the mariculture area of Dongshan Bay, China, for characterizing geochemistry (by using the European Community Bureau of Reference (BCR) sequential extraction procedure) and bioaccumulation of Hg and As [by calculating the biota sediment accumulation factor (BSAF)]. Both elements in sediments were mostly associated with the residual fraction (69.52–95.06% and 88.22–91.12% of the total concentration, respectively), followed by the oxidizable (bound to sulfides and organic matter) fraction (1.25–25.32% and 3.62–6.00%, respectively). However, Hg presented a higher bioaccumulation than As. Correlation analysis indicated that As in residual fraction and Hg in oxidizable fraction exert positive contributions (R = 0.927, P < 0.01 and R = 0.869, P < 0.05, respectively) on their own bioaccumulation factor. This indicated that P. undulata could adsorb both Hg in organic fraction and As in residual fraction from the sediments. Therefore, we should pay more attention to the potential dissolution and release of metals bound to sediments in the digestive tracts of marine organisms.     

Sorption behavior of Cd, Cu, Pb, and Zn and their interactions in phytoremediated soil

The aim of our study was to compare the sorption properties of a contaminated soil before and after two types of phytoremediation (natural phytoextraction vs. phytostabilization with dolomite limestone (DL) application). Soil from a pot experiment in controlled greenhouse conditions performed for two vegetation periods was used for the study. Lead, as the main contaminant in the studied soil, was easily desorbed by Cu, especially due to the increased affinity of Cu for soil organic matter; hence input of Cu to the studied soil can present another environmental risk in soils contaminated with other metals (such as Pb). In addition, the sorption behavior of chosen metals from single-element solutions differed from multielement solutions. The obtained results proved the different sorption behavior of metals in the single-element solution compared to the multi-element ones. Soil sorption behavior of Cd, Cu, and Zn decreased with the presence of the competitive metals; nevertheless, Pb sorption potential was not influenced by other competitive metals. Natural phytoextraction showed no significant effect on the sorption of Cd, Cu, Pb, and Zn onto the soil On the other hand, phytostabilization associated with DL application improved the soil sorption efficiency of all chosen metals, especially of Cu.     

模拟酸雨对污染土壤中Cd、Cu和Zn释放及其形态转化的影响

研究了模拟酸雨连续浸泡下污染红壤和黄红壤中重金属释放及形态转化．结果表明。随着模拟酸雨pH值下降,污染土壤中重金属释放强度明显增大;Cd、Zn释放量与酸雨pH值呈线性极显著负相关．Cu与酸雨pH值呈线性显著负相关．模拟酸雨作用下,污染红壤和黄红壤中Cd均以交换态为主;Cu则以有机结合态和氧化锰结合态为主;Zn在污染红壤中以残留态和交换态为主．在污染黄红壤中以残留态和有机结合态为主．土壤有机质含量和阳离子交换量对Cd、Cu、Zn的释放产生一定的影响并影响Cd、Zn的形态转化,但对Cu形态转化影响不明显,随着模拟酸雨酸度增大,污染红壤和黄红壤中重金属Cd、Cu的生物可利用态明显增多,但难解吸态Zn向生物有效态转化效应不明显．     

The distribution and bioavailability of Cd and Zn in cultivated soil of Henan Province

Abstract

Concentrations of surface soil Zn and Cd from agricultural areas of the Henan Province were measured. About 234 soil samples were collected. Total metal analyses, sequential chemical fractionation which were divided into seven fractions according to the method of the Geological Survey Technical Standard (DD2005-03) set by the China Geological Survey were carried out on the samples. Total Cd and Zn concentrations of the topsoil were 0.1909 (0.1–0.549) and 63.07 (33.3–344.3) mg kg^?1 respectively. Compared with the values permitted in China’s control standards for soil (GB 15618–1995) and background value in Henan Province, the soil samples showed high levels of Cd. The soil organic carbon has a significantly positive correlation with Cd and Zn concentration in the soil. Significant positive correlation between pH and Cd, Zn concentration was observed. On average, the order of Cd in each fraction was exchangeable, (27.3%)>weakly bound to organic matter; (22.7%)>strongly bound to organic matter; (16.4%)>residual; (15.1%)>carbonate; (12.1%)>Fe/Mn oxide bound; (4.5%)>water soluble; (2.0%), Zn was residual; (66.3%)>Fe/Mn oxide bound; (10.9%)> weakly bound to organic matter; (9.4%)> exchangeable; (6.0%)> strongly bound to organic matter; (3.9%)> carbonate (2.9%)> water soluble (0.6%). The accuracy of the sequential extraction was judged by the relative error (RE). RE for Cd ranged from 0 to 45% with a mean of 16.3%. RE for Zn ranged from 0.1 to 11.4% with a mean of 3.4%. On average, bioavailability index (BI) for Cd and Zn was 39.1% and 9.0% respectively. The mobility of the elements in the order Cd> Zn corresponds with the plant-availability of individual elements. Comparisons between activities of Cd²⁺ and Zn²⁺ calculated by Sauve semi-mechanistic equations and that of the water soluble fractions were demonstrated. The activities of Cd²⁺ and Zn²⁺ calculated by the semi-empirical equation are lower than its water soluble fraction.     

Distribution of extractable heavy metals in different soil fractions

Abstract

Due to the difficulties of precisely characterizing environmentally contaminated soil, the effects of heavy metals on plants are studied using uncontaminated soil spiked with known quantities of heavy metals. One problem in using spiked soils is how accurately the distribution of metals mimics stabilized natural soils. We studied the distribution of cadmium, chromium, copper, lead, nickel, and zinc in soil fractions after application in soluble form. The soil samples included a control (an uncontaminated Typic Argiudoll) and two samples spiked with either a moderate or high heavy metal concentration). After application of the salts the soils were subjected to wet/dry cycles over the course of three months. The soils were fractionated using a sequential chemical extraction procedure employing: (1) CaCl₂,(2) NaOH, (3) Na₂EDTA and (4) HNO₃, HCl, and HF. Soil physical separation was carried out by ultrasonic dispersion. The heavy metal levels were determined using ICP-AES. Each heavy metal displayed a unique behavior when added to soil in the form of soluble salts. Cadmium and zinc remained in the soluble fraction, indicating that no equilibrium was attained, while nickel primarily appeared in the insoluble fraction. Chromium, copper and lead were distributed among various soil chemical fractions. The highest levels of all metals appeared in the clay fraction except lead which was mainly present in the silt fraction.     

Heavy metals (Cu,Zn, Pb,Cd) in sediment,zooplankton and epibenthic invertebrates from the area of the continental slope of the Banc d'Arguin (Mauritania)

The concentrations of copper, zinc, lead and cadmium in the surface sediment (upper 5 mm) were generally higher in the silt fraction than in the bulk sediment. No significant geographical trend in the metal concentrations of the surface sediments was found, nor a correlation between concentrations in bulk sediment as well as in the silt fraction and the % silt could be established. In general, the metal concentrations in both bulk sediment and silt are lower, when compared to marine environments in other climatological regions.In zooplankton, the metal concentrations were relatively high: expressed in µg g^–1 on a dry weight (D.W.) basis, they ranged from 15–90 for copper, 70–580 for zinc, 12–55 for lead and 4–10 for cadmium.In epibenthic invertebrate species, both in crustaceans and bivalve molluscs, the concentrations of copper, zinc, and lead were in the same order of magnitude as compared to corresponding species from other geographical latitudes. Cadmium concentrations were relatively low, ranging from 0.13–0.42 µg g^–1 D.W. in the bivalve molluscs Pitaria tumens and from 0.04–0.27 µg g^–1 D.W. in the shrimp Processa elegantula. Also in the crab species Ilia spinosa, Inachus sp. and Pagurus sp., the cadmium concentrations were low, varying between 0.1 and 0.2 µg g^–1 D.W.No significant relation between the metal concentration in whole-body samples and sediment (either bulk or silt) was present. Also no gradient was apparent in concentrations in organisms sampled at different depths (5 to 200 m) along two off-shore transects perpendicular to the Banc d'Arguin. Data indicated lower metal concentration in epibenthic organisms from sampling stations along a northern transect (southwest of Cap Blanc) than in organisms from the southern transect, off Cap Timiris.Evidence was obtained for a considerable atmospheric input of heavy metals, in particular zinc and lead, in a certain area along the continental slope of the Banc d'Arguin.     

Leaching of Cd,Zn, Pb,and Cu in Packed and Undisturbed Columns of Soils Affected by the Spill from a Pyrite Mine in the South of Spain

A study has been made of the leaching of Cd, Zn, Pb, and Cu in three representative soils within the zone affected by the spill from a pyrite mine in Aznalcollar (Sevilla, Spain) employing packed soil columns. According to the breakthrough and cumulative leaching curves, the relative mobilities of the different toxic elements in the columns are as follows: Cd> Zn> Cu> Pb. The effect of leaching on the distribution of metals as a function of depth using intact soil cores was also studied. The results showed that the soils themselves have a good capacity for immobilizing the soluble fraction of the elements from the spilled mud. This capacity varied as follows: clayey soil with a high carbonate content > clayey soil with a moderate carbonate content > sandy-clay loam soil with a low carbonate content. However, sandy soils with a low carbonate content could pose a risk to groundwater if initial contamination was high. These results could be considered during the evaluation of remedial technologies for the immobilization of soil metals.     

Continuous Biosorption of Pb,Cu, and Cd by Phanerochaete chrysosporium in a Packed Column Reactor

The dynamic removal of lead, copper and cadmium in a single component system by Phanerochaete chrysosporium was studied in packed columns. The packed columns consisted of biomass of P. chrysosporium immobilized on polyurethane foam cubes. The performances of packed columns were described through the concept of breakthrough and the values of column parameters predicted as a function of bed depth. The column biosorption data were evaluated in terms of maximum (equilibrium) capacity of the column, the amount of metal loading and the yield of the process. The maximum capacities for lead, copper and cadmium were 70.7, 43.7 and 70.8 mg, respectively, and their yields were 39.2, 40.6 and 41%, respectively. The kinetic and mass transfer aspects of the dynamic removal of the three metals were studied using three mathematical models commonly used to describe the column performance in adsorption processes. Column studies showed good agreement between the experimental data and the simulated breakthrough curves obtained with Adams-Bohart or the Wolborska model and the Clark model. While the initial segment of the breakthrough curve was defined by the Adams-Bohart and Wolborska models, the whole breakthrough curve was well predicted by the Clark model for all the three metals studied.     

Time evolution of Pb(II) speciation in Pampa soil fractions

Abstract

Soil pollution by heavy metals, particularly lead, is an important environmental concern; the bioavailability of such pollutants is strongly dependent on their chemical form. Here, the speciation of Pb(II) in soil fractions as a function of time shortly after its incorporation is studied, using a selective sequential extraction method. The sample came from an Argentinean Pampas region and was extensively characterised, including Rietveld analysis of the silt+clay fraction XRD pattern to find the major mineral components. Experiments were run twice, once in the winter and once in the summer. The results show different speciation time profiles in both cases, showing faster changes in winter due to the higher water content. The summer experiment corresponds to an earlier stage in the speciation profile evolution compared with winter. The soluble/exchangeable fraction decreases with time in summer but shows a lower and constant value in the winter. A high proportion is found to be adsorbed onto the stable (aluminosilicates+quartz) mineral fraction. The results strongly suggest that, even at a short time following soil pollution with Pb, a high proportion is adsorbed onto the mineral fraction, with only a low fraction being bioavailable. The most stable (mineral incorporated) form is observed to increase with time. Soil water content appears to be more important than temperature in determining the differences between the two.     

Vertical and Horizontal Distributions of Zn,Cd, Pb,Cu, and Hg in Uncultivated Soil in the Vicinity of a Zinc Smelter at Odda,Norway

In the present work the extent and variation of Zn, Cd, Pb, Cu, and Hg loading in undisturbed surface soil (0–5 cm) and the vertical transport of the metals in soil profiles are studied in the vicinity of a zinc smelter in Norway. Three major controlling factors on the metal concentrations in soil have been assessed: 1) distance from the anthropogenic point source; 2) organic matter content (O.M.); and 3) the prevailing wind directions. Moreover metal distributions in proximal soil profiles in 1972 and 2003 are compared. Current concentrations of Zn, Cd, Pb, Cu, and Hg in surface soil reach 14000, 60, 980, 430, and 7.0 mg·kg ^{? 1} , respectively, near the smelter and decrease regularly with distance in the northerly direction according to the regression model (y = ax^{? b} ). The Zn concentrations are significantly different from the background range up to 30 km from the smelter, whereas the other metals approach background at only 10 km distance. Subsurface concentration peaks of Pb, Cu, and Hg are found at greater depth in soil profiles than peaks of Zn and Cd. Levels of Zn, Cd, and Pb in surface soil seem to have decreased from 1972 to 2003, whereas for Cu the levels appear not to be significantly different.     

Removal of Cd2+, Pb2+, and Zn2+ from contaminated water using dolomite powder

Dolomite collected from Surat Thani Province in Thailand was investigated for use as a sorbent for the removal of divalent heavy metal cations from an aqueous solution. The sorbent had a surface area of 2.46 m²/g and a pH of zero point charge (pHzpc) of 9.2. Batch sorption was used to examine the effect of the pH (pH 3–7) on the sorption capacity of Cd²⁺, Pb²⁺ and Zn²⁺, alone or together as an equimolar mixture at various concentrations. Alone, each heavy metal cation was adsorbed faster at a higher pH, where the sorption of Cd²⁺ and Pb²⁺ fitted a Langmuir isotherm, but Zn²⁺ sorption best fitted a Freundlich isotherm. Under equimolar competitive sorption, the sorption capacity of each cation was decreased by 75.8% (0.29–0.07 mM/g), 82.8% (0.53–0.09 mM/g), and 95.7% (0.84–0.04 mM/g) for Cd²⁺, Pb²⁺ and Zn²⁺, respectively, compared to that with the respective single cation. Desorption of these heavy metal cations from dolomite was low, with an average desorption level of 0.06–17.4%. Furthermore, since dolomite is readily available and rather cheap, it is potentially suitable for use as an efficient sorbent to sorb Cd²⁺ and Pb²⁺, and perhaps Zn²⁺, from contaminated water.     

The action of divalen Zn,Cd, Hg,Cu and Pb ions on the ATPase activity of a plasma membrane fraction isolated from roots ofZea mays

The effects of the divalent metal ions Zn, Cd, Hg, Cu and Pb on the ATPase activity of a plasma membrane fraction isolated from roots ofZea mays have been investigated. When Mg-ions (3 mM), with or without K-ions (50mM) are included in the reaction medium, inhibition of ATPase activity was found in all cases, the relative order of the inhibitors over the concentration range 10 to 100M, being Hg>>CuCd>ZnPb. Below 1.0M only Hg caused substantial inhibition. In the absence of Mg ions, Zn and to a lesser extent Cd, activated the enzyme up to a concentration of 1 mM, activity being further stimulated in the presence of K-ions (50mM). No activation of ATPase activity was found for Hg, Cu or Pb. It was concluded that Zn-ATP and Cd-ATP are both alternative substrates for the enzyme. Further experiments showed that both K_m and V_max for the substrates Zn-ATP and Cd-ATP are very much lower than for the usual substrate Mg-ATP.These present results are discussed in relation to the known actions of these divalent cations on the trans-root potential and H-ion efflux in excised maize roots (Kennedy and Gonsalves, 1987).