Distribution, movement and availability of Cd and Zn in a dredged sediment cultivated with Salix alba

Willows occur as volunteer vegetation on sediment-derived soils, such as dredged sediments, landfill cover or stockpile deposits, and are used as phytoremediators on such soils. The present study evaluates growth and metal uptake by Salix alba grown on a contaminated dredge sediment for 209 days under greenhouse conditions. At the end of the study, the aerial parts of the S. alba plants had grown to heights of between 80 and 117 cm. Biomass and Cd and Zn concentration in the roots, stems and leaves, at 70, 112 and 209 days, showed that Cd and Zn had been bioaccumulated, especially in the leaves.At the three sampling dates, Cd and Zn extractability and pH measurements were also carried out on samples of two soil layers (0–15 and 15–30 cm) from both the planted and the control pots. Cd and Zn extractability were assessed using single extraction procedures (0.01 M CaCl₂; 1 M HNO₃; CaCl₂–TEA–DTPA). The two metals showed similar variations in CaCl₂ and HNO₃ extractabilities, but this was not the case for DTPA extractability. The greatest variations were observed in the upper soil layers of the control pots. In the planted pots, the CaCl₂ extractability of Zn decreased in the upper layer, and the HNO₃ extractability of Zn increased in the lower layer. The pH of the upper soil layer was always higher than the pH of the bottom layer. In addition, we monitored several parameters of the percolates from both the planted and the control sediments, including pH, Eh, conductivity, dissolved organic carbon, Zn and Cd concentrations, and presence of certain cations/anions. Dissolved organic carbon, and Cd and Zn concentrations increased steadily over time. There were no significant differences between the planted and the control pots. After 209 days, the characteristics of the control sediment reflected the effects of ageing in that the CaCl₂-extractable Cd and Zn concentrations had decreased compared with the initial concentrations. Conversely, the concentrations of HNO₃-extractable Cd and Zn had increased. A fraction of the metal initially extracted by CaCl₂ (considered as exchangeable) became less available with time. After 112 days, the plants had extracted approximately 2.8 mg of Zn. At the same time, the CaCl₂ extractability of Zn in the upper, rooted layer decreased by 2.6 mg. We can assume that S. alba extracted Zn from the pool of CaCl₂-extractable Zn.     

Factors influencing the potential mobility and bioavailability of metals in dried lake sediments

Abstract

Samples taken from polluted creek sediments were dried at temperatures between 20°C and 100°C (either in air or under a nitrogen atmosphere) and selective chemical extraction procedures were then used to examine the effect of drying temperature and oxidation on the bonding mode distribution patterns of Zn, Pb, Cd and Cu. Exposure to air during the drying stage tended to increase the fraction of total metal which was less firmly bound (i.e. ion exchangeable, weakly sorbed). Less metal was present in these categories when higher drying temperatures were used, and temperature changes had a larger effect when the samples were dried under nitrogen. The drying process appears to promote metal migration to phases having a stronger bonding power. In most of the samples studied, heating caused Pb to migrate to the carbonate phase while accumulation in the organic/sulfide phases was the dominant process for Cu and Cd. In the case of Zn, migration to the carbonate phase was favoured in some studies (e.g. using air-dried samples), in other sediments the migration end-point was the organic/sulfide phases. During storage of dried samples at room temperature for prolonged periods (e.g. months) the amount of less firmly bound metal tended to increase, and nullified the distribution changes induced by drying. The effect was most pronounced in the case of Cd. The study highlights that significant errors in metal distribution pattern analyses can arise from sample preparation procedures and it has provided information on the possible mobilisation of metal when dredged sediment is land-dumped, i.e. allowed to dry in air.     

Experimental Study of Mobility and Kinetic Characterization of Trace Elements in Contaminated Sediments from a River Basin in Northern Peru

In the Jequetepeque basin (Peru), gold extraction activity has been performed in the last decades, leading to a release of metals and metalloids into the environment. Sediment samples were taken in the vicinity of two mines and analyzed. Extraction of metals and metalloids from sediments was carried out using single extraction procedures, acidic (HNO₃), and complexation (EDTA) leaching, in order to determine the mobility of trace elements. Results indicated that acidic extraction at low pH values increased the leachability of trace elements. EDTA showed a higher bioavailability of metals in sediments than acidic extraction under similar pH conditions because of its greater leaching capacity. This is an important issue in view of risk assessment analysis. The highest extractability was observed for Cd in all sediments with up to 90% of extraction after 1 h. The mobility index analysis indicated that faster kinetic leachability of some trace elements leads to a higher mobility in sediments, especially those near the active gold extraction mine. The ecological risk assessment suggested that the four river sediments were at high and very high risk levels, indicating that sediment contamination is an issue of environmental concern in the Jequetepeque basin of northern Peru.     

Factors influencing the potential mobility and bioavailability of exchangeable ammonium ion in dried lake sediments

Abstract

The effect of drying temperature and oxidation on the level of exchangeable ammonium ion found in sediments has been examined using samples collected from along a polluted creek and from shallow lake bays. The sediments were dried at temperatures between 20°C and 100°C (either in air or under a nitrogen atmosphere), and the ammonium ion content was extracted into 0.1 M KCl prior to analysis using an ion selective electrode. Exposure to air during the drying stage usually resulted in lower ammonium values, while increasing the drying temperature altered the amount of displaceable (i.e. available) ammonium ion extracted, generally in an upward direction. The amount detected (5–25 μ g^?1) varied between sites, and surface sediment values differed from the 10–50 cm core material results. The pH of the extracts varied with the drying temperature used, indicating that the heating process promoted some chemical changes in the test samples. The study has demonstrated that in nutrient level surveys, the analytical data produced can depend greatly on the sample preparation procedure selected. It also indicated the type of changes which could occur when dredged sediments are land dumped.     

EVALUATION OF PIGMENT EXTRACTION METHODS AND A RECOMMENDED PROTOCOL FOR PERIPHYTON CHLOROPHYLL a DETERMINATION AND CHEMOTAXONOMIC ASSESSMENT1

Many methods have been proposed to extract and quantify algal pigments. Comparative studies have found that pigment extraction efficiency varies among solvent and mechanical disruption protocols due to differential cellular resistance, thereby, leading to potential misinterpretation of pigment data. When the type or resistance of algae are unknown, a method is required that efficiently extract pigments from all taxonomic groups. The objective of this study was to develop a simple and efficient one stage periphyton pigment extraction protocol by comparing the extractability of four solvents (acetone, methanol, methanol/acetone, and methanol/acetone/N,N‐dimethylformamide), the effects of grinding, and the effects of freeze‐drying. The best overall extraction was obtained using freeze‐dried samples extracted with methanol/acetone/DMF/water (MAD). Eighty‐six percent more chlorophyll was extracted when the sample was freeze‐dried relative to fresh/frozen samples extracted with 90% acetone. Freeze‐drying greatly improved the extraction of both polar and non‐polar (lipophilic/hydrophobic) pigments while MAD increased the extractability of polar pigments and improved peak resolution of all pigments. Chemotaxonomic assessment differed between samples that were fresh/frozen or freeze‐dried before extraction. The relative abundance of cyanobacteria was greater for freeze‐dried material compared with fresh/frozen due to the improved extractability of cyanobacterial pigments. Based on the results of this study, the traditional approach of 90% acetone as a solvent is not recommended for periphyton samples containing cyanobacteria or when the composition of the mat is unknown. The combination of freeze‐drying and MAD was sufficient for the extraction of pigments from a periphyton mat containing filamentous cyanobacteria, green algae, and diatoms.     

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.     

The influence of composting and maturation processes on the heavy-metal extractability from some organic wastes

Seven mixtures from four organic residues—aerobic sewage sludge, city refuse, peat residue and grape debris—were made up to study the influence of the composting and maturation processes on the extractability of Fe, Cu, Ni, Zn, Cd, Pb, Cr and Mn by a chelating agent (diethylenetriaminepentaacetic acid, DTPA) and a neutral salt solution (0·05m CaCl₂) from the residues.Composting and maturation increased the concentration of heavy metals in the materials due to the loss of weight of the materials during these processes. The metals also became more insoluble, and extractants employed removed larger amounts of metals from the raw composts than from the mature composts. In general, CaCl₂-extractable metals did not correlate significantly with the metal content of the composts. With DTPA-extractable metals, the only ones that showed significant correlations between the quantity of metal extracted by DTPA and the metal content of the samples in nearly all the composts studied were Pb and Zn.The load of ‘zinc equivalent’ increased with the composting and maturation processes, and the Cd/Zn ratio decreased with those processes.     

Assessment of Heavy Metal Mobility in Dredged Sediments: Porewater Analysis,Single and Sequential Extractions

Dredged sediments from the Leie catchment (Belgium) that were deposited on land between 70 and 10 years ago were characterized according to their physico-chemical properties, total metal concentrations and porewater composition. Actual and potential heavy metal availability was assessed by means of single extractions with 0.01 M CaCl ₂ , 0.05 M EDTA and 0.43 M acetic acid. A modified version of the BCR (Community Bureau of Reference) extraction procedure, adapted to the elevated acid neutralizing capacity of the sediments, was applied. Information on element mobility was assessed and the used methodologies were critically evaluated.

The favorable physico-chemical characteristics of dredged sediments from the catchment of the Leie River (N-Belgium) indicated a rather low actual heavy metal mobility. Based on CaCl ₂ and EDTA extractions, the distribution of Cd, Zn and Ni between the solution and sorbed phase could be described as a function of pH and organic carbon content. Cd and Zn were found to be the elements with the highest potential availability, while Cu and Ni displayed a medium availability. It is stressed that different types of extractions deal with heavy metal mobility in a different way and that the measurement of “key-factors” such as the pH of the extracts can be helpful for the interpretation of the results.     

Solid-phase distribution of heavy metals as affected by single reagent extraction in dredged sediment derived surface soils

ABSTRACT

EDTA is useful to assess mobile metal pools in polluted soils and sediments. There is a need to enhance our understanding of the significance of metal fractions released. The impact of single reagent extraction with 0.05 mol L^?1 EDTA on the solid phase distribution of trace metals in surface soils sampled from confined dredged sediment disposal sites was investigated. Not extracted and EDTA extracted soils were subjected to sequential extraction to fractionate the total contents into: (1) easily exchangeable and carbonate bound fraction; (2) reducible fraction; (3) oxidisable fraction; and (4) residual fraction. With EDTA, significant portions of metals associated with the acid extractable and reducible fractions were released. The oxidisable and residual fractions remained unaffected for most of the investigated metals except for the organic matter associated metals (Cu and Pb). A decrease in the residual fraction after EDTA-extraction for Cu and Pb was attributed to artifacts of the sequential extraction procedure.     

Extractability and biological activity of tannins from various tree leaves determined by chemical and biological assays as affected by drying procedure

Leaf samples of Juglans regia (walnut), Rhus typhina (sumach), Aesculus hippocastanum (chestnut) and Salix alba (willow) were either freeze dried or oven dried and the amount of tannins was determined by two chemical assays (Folin Ciocalteau and ferric chloride method). In addition, the biological activity of these tannins was determined by their protein precipitation capacity and by a bioassay based on the incubation to the leaves in vitro in buffered rumen fluid with and without polyethylene glycol. Generally, oven drying is recognised to decrease the extractability and/or the biological activity of tannins. Our results however do not indicate a general decrease in extractability of tannins due to oven drying. The effects observed were plant specific with negative effects of oven drying in walnut and willow leafs, positive effects in chestnut leaves and no effects were observed for the sumach. No negative effects of oven drying were detected for the biological activity of the tannins. The specific protein precipitation capacity was nearly identical for the freeze dried and the oven dried tannins. Oven drying however decreased the solubility of the cell contents and the plant cell wall, which led to changes in fermentation end products, but the biological activity of the tannins was not negatively affected by the oven drying. Although some differences in the extractability and activity of the individual plant species were observed, we conclude from this work that the drying procedure has no negative effect on the biological activity of the tannins examined.     

Chemical mobility and bioavailabity of sediment-bound heavy metals influenced by salinity

The transfer of metals from contaminated sediments to algal cell walls (Scenedesmus quadricauda) and organisms from various trophic levels (euryhaline osmoconform hydroid Cordylophora caspia and algae Brachiomonas submarina) was studied with a multichamber device. The system consists of a central chamber which contained the mud suspension and six external chambers containing the different biological indicators. The solids in the central and external chambers are separated by 0.45 m-diameter membranes which allow diffusion of the mobilized, dissolved metal compounds. Experiments were performed with dredged sediments at various salinities (0.5, 1.0, 1.5, and 2.0 percent, respectively) and the kinetic of re-adsorption was obtained by taking samples after different time intervals. High enrichment of Cd was found in the living alga Brachiomonas submarina, but on the other side only a weak influence of salinity on re-adsorption could be observed. Model experiments with ionic Cd showed a clear dependency on Cd-sorption on the algae, Cd-concentration in solution, and salinity. These results indicate that the transfer of metals mainly depends on the specific surface properties of the substrates and on the specific chemical form of the dissolved mobilized metal.     

Effects of soil acidification on the chemical extractability of Fe,Mn, Zn and Cu and the growth and micronutrient uptake of highbush blueberry plants

Summary The effects of soil acidification and micronutrient addition on levels of extractable Fe, Mn, Zn and Cu in a soil, and on the growth and micronutrient uptake of young highbush blueberry plants (Vaccinium corymbosum L. cv. Blueray) was investigated in a greenhouse study.Levels of 0.05M CaCl₂-extractable Fe, Mn, Zn and Cu increased as the pH was lowered from 7.0 to 3.8. However, the solubility (CaCl₂-extractability) of Fe and Cu was considerably less pH-dependent than that of Mn and Zn. With the exception of HCl-and DTPA-extractable Mn, micronutrients extractable with 0.1M HCl, 0.005M DTPA and 0.04M EDTA were unaffected or raised only slightly as the pH was lowered from 6.0 to 3.8. Quantities of Mn and Zn extractable with CaCl₂ were similar in magnitude to those extractable with HCl, DTPA and EDTA whilst, in contrast, the latter reagents extracted considerably more Cu and Fe than did CaCl₂. A fractionation of soil Zn and Cu revealed that soil acidification resulted in an increase in the CaCl₂- and pyrophosphate-extractable fractions and a smaller decrease in the oxalate-extractable fraction.Plant dry matter production increased consistently when the soil pH was lowered from 7.0 to 4.6 but there was a slight decline in dry matter as the pH was lowered to 3.8. Micronutrient additions had no influence on plant biomass although plant uptake was increased. As the pH was lowered, concentrations of plant Fe first decreased and then increased whilst those of Mn, and to a lesser extent Zn and Cu, increased markedly.     

Accumulation of heavy metals by aquatic mosses. 1: Fontinalis antipyretica Hedw.

An account is given of methods developed to monitor heavy metals in rivers by measuring the concentration of these metals in Fontinalis antipyretica Hedw. Key features of the standard method recommended include the harvesting of materials from microhabitats with fast current speeds wherever possible, thorough washing in field and laboratory, use of terminal 2-cm lengths of shoot, drying at 105°C and digestion in 2 M HNO₃. In order to establish the extent to which this species is useful and to provide baseline data with which others can compare their own observations, samples of moss, water and sediments were harvested for analysis from 52 different sites in northern England and Belgium. Significant positive correlations were obtained between Cu and Zn in 2-cm tips and in both (total) water and sediment, but in the case of Cd and Pb only between 2-cm tips and sediment. Multiple stepwise regression was used to quantify the apparent influence of environmental variables. For instance, with Pb in the moss as the dependent variable, significant influences were found for Zn in the moss (+ve) aqueous Mn (+ve) and filtrable reactive phosphate (?ve). Variables which were significant were incorporated in each case into equations to predict the concentration of metal that would be expected if allowance was made for the concentrations of all these variables at each site. In the case of Pb, r² = 0.075 for metal in moss versus aqueous metal, whereas r² = 0.879 for metal in moss versus the predicted value for metal in moss. This suggests that the lack of correlation between Pb in moss and Pb in water was probably due largely to the influence of other variables. For Cd, the difference was less: r² = 0.013 and r² = 0.47, respectively. A principal components analysis was also carried out, with measurements of water and moss as the variables ordinated. An example is given of the use of the moss to monitor intermittent Zn pollution in R. Wear.     

Bioavailability and crop uptake of trace elements in soil columns amended with sewage sludge products

In order to assess the potential impact of long-term sewage sludge application on soil health, the equivalent of about 25 years of agronomic applications of low-metal (`EQ') sewage sludge products were made to greenhouse soil columns. After a 6-year period of `equilibration', during which time successive crops were grown with irrigation by simulated acid rain, the plant-available quantities of trace elements were estimated in the soils by extraction with 0.01 M CaCl₂ at 90 °C, and measured directly by uptake into a crop of red clover (Trifolium pratense L.). Soil pH had a strong influence on the level of extractable and plant-available metals, and because the tested sludge products affected soil pH differently, pH was directly factored into the comparison of different sludge treatments with controls. CaCl₂-extractable levels of several metals (Cu, Zn, Mo), sulfur and phosphorus were found to be higher in the soils amended with organic-rich sludge products than in the control soils. However, extractable Cd and Ni were not significantly elevated by the sludge amendments, presumably because of the low total loading of these metals. Copper, Zn and Mo applied in the form of sludge ash had low soil extractability, suggesting that these trace metals were trapped in high-temperature mineral phases formed during sludge incineration, and resisted subsequent weathering in the soil environment. Extractable soil metals in the alkaline-stabilized sludge treatment were also generally low. Phytotoxicity from the sludge metal loadings (Zn≤125, Cu≤135 kg/ha), was not clearly indicated as long as soil pH was maintained in the 6–7 range by lime amendment. Nevertheless, unexplained depressions in yield were noted with some of the sludge products applied, particularly the dewatered and composted materials. On limed soil columns, the most consistent effect of sludge product amendment on red clover composition was a marked increase in plant Mo.     

Nitrification and denitrification response to varying periods of desiccation and inundation in a western Kansas stream

Changing environmental conditions and increased water consumption have transformed many historically perennial stream systems into intermittent systems. Multiple drying and wetting events throughout the year might impact many stream processes including nitrification and denitrification, key components of the nitrogen (N) cycle. During summer 2007, an experimental stream was used to dry and then rewet stream sediments to determine the effects of desiccation and rewetting of stream sediment on nitrification and denitrification potentials. Mean (±SE) nitrification and denitrification rates in sediment not dried (controls) were 0.431 ± 0.017 μg NO₃ ⁻–N/cm²/h and 0.016 ± 0.002 μg N₂O–N/cm²/h, respectively. As sediment samples dried, nitrification rates decreased. Rates in sediments dried less than 7 d recovered to levels equal or greater than those in the controls within 1 d of being rewetted. Denitrification rates were not affected by 1 d of drying, but samples dried greater than 1 d experienced reduced rates of denitrification. Denitrification in sediments dried 7 d or less recovered by day seven of being rewetted. Nitrification and denitrification processes failed to fully recover in sediments dried more than 7 d. These results demonstrate that alterations in stream’s hydrology can significantly affect N-cycle processes.     

Pollution characteristics and ecological risk assessment of heavy metals in the surface sediments from a source water reservoir

Surface sediment samples were collected from a source water reservoir in Zhejiang Province, East of China to investigate pollution characteristics and potential ecological risk of heavy metals. The BCR sequential extraction method was used to determine the four chemical fractions of heavy metals such as acid soluble, easily reducible, easily oxidizable and residual fractions. The heavy metals pollution and potential ecological risk were evaluated systematically using geoaccumulation index (I_geo) and Hakanson potential ecological risk index (H′). The results showed that the sampling sites from the estuaries of tributary flowing through downtowns and heavy industrial parks showed significantly (p < 0.05) higher average concentrations of heavy metals in the surface sediments, as compared to the other sampling sites. Chemical fractionation showed that Mn existed mainly in acid extractable fraction, Cu and Pb were mainly in reducible fraction, and As existed mainly in residual fraction in the surface sediments despite sampling sites. The sampling sites from the estuary of tributary flowing through downtown showed significantly (p < 0.05) higher proportions of acid extractable and reducible fractions than the other sampling sites, which would pose a potential toxic risk to aquatic organisms as well as a potential threat to drinking water safety. As, Pb, Ni and Cu were at relatively high potential ecological risk with high I_geo values for some sampling locations. Hakanson potential ecological risk index (H′) showed the surface sediments from the tributary estuaries with high population density and rapid industrial development showed significantly (p < 0.05) higher heavy metal pollution levels and potential ecological risk in the surface sediments, as compared to the other sampling sites.     

Gewinnung und Charakterisierung von Proteasen aus Thermoactinomyces vulgaris. VI. Mitt. Zur Herstellung eines Trockenpraparates im Labor- und kleintechnischen Mnßstab unter besonderer Berücksichtigung des Öleinflusses

A dried proteolytic enzyme preparation “Thermitase” is produced of the cultural solution of Thermoactinomyces vulgaris. The procedure comprises concentration, sedimentation, ethanol and sodiumsulfate precipitation and drying in laboratorial and semitechnical scale. The elimination of rape seed oil which impairs the salt sedimentation was specially taken into account. A certain sedimentation procedure using caoline or a aqueous solution of CaCl₂ and Na₂HPO₄ or filtration was elaborated to eliminate the lipid components in the concentrated solution. The method is convenient to get good yields of the thermostable protease.     

Distribution and chemical fractionation of some heavy metals in bottom sediments of Lake Nasser

Distribution and phase association of Cd, Cr, Cu, Fe, Mn, Ni,Pb, Zn and organic matter in Nile sediments taken from LakeNasser (Aswan, Egypt) were investigated. The sediment sampleswere subjected to selective chemical extraction proceduresdesigned to fractionate the particulate heavy metals into sixfractions: (A) ammonium acetate-extractable metals; (B) sodiumacetate-extractable metals; (C) acid oxalate-extractablemetals; (D) hydroxylamine HCl-extractable metals; (E) aquaregia-extractable metals and (F) total metals (HF/HCl/HNO₃destruction). Exchangeable metals which can be extracted byammonium acetate solution are generally considered readilybioavailable as they are weakly bound and may equilibrateeasily with the aqueous phases. In the present study very smallconcentrations of all heavy metals considered were found inthis phase. Between this phase and the metal phases which arenot bioavailable (those exist in highly resistant phases) thereexist several geochemical phases (fractions B, C & D) that maypotentially release their associated metals under changingenvironmental conditions, such as pH and redox potential in thewater sediment interface. This revised version was published online in July 2006 with corrections to the Cover Date.     

Bioavailability and Concentration of Heavy Metals in the Sediments and Leaves of Grey Mangrove, <Emphasis Type="BoldItalic">Avicennia marina</Emphasis> (Forsk.) Vierh,in Sirik Azini Creek,Iran

The concentration and bioavailability of Ni, Cu, Cd, Zn, and Pb in the sediments and leaves of grey mangrove, Avicennia marina, were studied throughout Sirik Azini creek (Iran) with a view to determine heavy metals bioavailability, and two methods were used. Results show that Zn and Ni had the highest concentrations in the sediments, while Cd and Cu were found to have the lowest concentrations in the sediments. Compared to the mean concentrations of heavy metals in sedimentary rock (shales), Zn and Cu showed lower concentration, possibly indicating that the origin of these heavy metals is natural. A geo-accumulation index (I _geo) was used to determine the degree of contamination in the sediments. I _geo values for Zn, Cu, Pb, and Ni showed that there is no pollution from these metals in the study area. As heavy metal concentrations in leaves were higher than the bioavailable fraction of metals in sediments, it follows that bioconcentration factors (leaf/bioavailable sediment) for some metals were higher than 1.     

Effects of biochar amendments on speciation and bioavailability of heavy metals in coal-mine-contaminated soil

An incubation experiment was executed on applying biochar as a soil remediation amendment to discuss an effect of the various addition rates on the speciation and bioavailability of heavy metals in mining-contaminated soil. The result showed that the content of Cd in soil was 9.51 times higher than the Huainan soil background values. The contents of Cu, Zn and As were 2.97, 1.60 and 1.42 times the background values, respectively, and the total contents of all heavy metals were higher than the standard values of soil environment quality GB15618-1995 set by the China Ministry of Environmental Protection. Speciation analysis indicated that Cu and Cd were mainly associated with the reducible fraction, while Zn and As were dominated by the residual fraction. After biochar was added to contaminated soil, the residual fractions of heavy metals increased, while the acid-soluble fractions reduced. According to the results of CaCl₂ extraction experiment, CaCl₂-extractable concentrations of Cu, Zn, As, and Cd were observed with a biochar dosage rate of 10%, which were 57.26%, 51.37%, 6.94% and 42.04% lower than those of control soil samples, respectively, but there were no obvious changes of CaCl₂-extractable As.