Behavior of Cu and Zn under combined pollution of 2,4-dichlorophenol in the planted soil

Behavior of heavy metals under combined pollution of 2,4-dichlorophenol (2,4-DCP) was investigated using metal contaminated soil which was sampled from the heavily industrialized areas, Fuyang county, Zhejiang Province, P.R. China and pretreated with 100 μg g^?1 2,4-DCP for 1 month. Metal complexes were the predominant species for Cu and Zn in the soil solution. The treatment of 2,4-DCP had limited effect on the dissolution of Cu and Zn in the soil without plant root growth. But the metal species might be changed due to the addition of organic pollutant. Planting with rye grass for 1 month, greatly increased both water soluble Cu and Zn. The increase of water soluble Cu and Zn in the presence of 2,4-DCP was much more than that in the absence of 2,4-DCP, which suggested more attention should be paid to the behavior of heavy metals under combined pollution of organic pollutants in the planted soil. The results also indicated that in comparison to Cu, soil planted with ryegrass was more effective in activating Zn from soils, which was consistent with its relative weak chemisorptions on clays, oxides and humus of soils.     

Alkaline Soil Extraction and Subsequent Mineralization of 2,6-Dichlorophenol in a Fixed-Bed Bioreactor

Soil contaminated with moderate concentrations (0.1 g to a few grams) of several chlorophenol (CP) congeners can be remediated by a combination of alkaline extraction and mineralization of the extracted CP in a bioreactor. This method could substitute energy-demanding thermal treatment or space-requiring composting of moderately CP-contaminated soils. 2,6-dichlorophenol (2,6-DCP) served as a model compound to study the alkaline extraction of a loamy sand soil, followed by a biological treatment of the extract. Alkaline extraction is shown to be applicable to different types of soil and a wide range of chlorophenol concentrations. Soil washing was optimal with 10 mM NaOH (pH 12). The procedure yielded 2,6-DCP comparable to amounts obtained by Soxhlet- or ethanol-extraction. With the model soil used in this study, three subsequent extraction steps led to 97% removal of the initially spiked 6.17 mmol 2,6-DCP × kg^-1 soil (=1 g/kg), thus reaching the remediation goal of ≤ 0.2 mmol/kg remaining contaminant concentration. The resulting aqueous extract contained up to 6.8 mM 2,6-DCP and was treated in an aerobic fixed-bed bioreactor. The extraction medium was fed into a recirculation loop in order to dilute the pollutant to concentrations tolerated by the mixed bacterial culture in the reactor. 2,6-DCP was degraded to below the quantification limit (1.8 μiM), and significant detoxification was reached at volumetric loading rates up to 2.1 g/L-d.     

A field lysimeter study of heavy metal movement down the profile of soils with multiple metal pollution during chelate-enhanced phytoremediation

The agricultural soils near a copper smelter in southeast China were found to be highly contaminated with Cu, Pb, Zn, and Cd. Metal migration from the soil to groundwater presents an environmental risk that depends on the physicochemical properties of the contaminated soils. Soil solution samples were obtained using lysimeters from a loam soil with multiple metal pollutions over a period of about 1 yr. A field lysimeter study was also conducted to examine the potential use of (S, S')-ethylenediamine-N, N'-disuccinic acid trisodium salt (EDDSNa3) in chelate-enhanced phytoremedation and to evaluate the leaching of heavy metals. The average heavy metal concentrations in the soil solution (without the addition of EDDS) were high (e.g., 0.15 mg Pb L(-1) at a 50-cm depth) compared to the upper limit for protection of groundwater in China, but varied during the sampling period. Cu concentrations were not correlated with pH or dissolved organic carbon (DOC), but Zn and Cd concentrations were related to soil solution pH. EDDS enhanced metal solubility in the soil, but plant metal uptake by Elsholtzia splendens Nakai did not increase accordingly. There may be an increasing risk of groundwater pollution by Cu and the EDDS enhanced phytoremediation technique needs to be carefully applied to minimize this side effect.     

Simultaneous extraction of soil phytoavailable cadmium,copper, and lead by chelating resin membrane

Cadmium, copper, and lead were extracted from suspensions of contaminated soils using metal chelating exchange resin membranes. Nine soils with widely varying properties and Cd, Cu and Pb levels were tested. Soil suspensions made up with 4 g in 40 mL deionized water were equilibrated with 5 cm² Ca-saturated Chelex exchange resin membrane which was retained inside a polypropylene bag and shaken at 150 rpm for 24 hrs. Resin membrane extractable Cd, Cu and Pb of the soils were correlated with Cd, Cu, and Pb uptake by young wheat seedlings grown in these soils and compared with soil Cd, Cu, and Pb extracted by 0.1 M HCl, 0.01 M CaCl₂, and 0.005 M Diethylenetriamine pentaacetic acid (DTPA). The amounts of Cd, Cu and Pb extracted by the Ca-saturated Chelex membrane from all tested soils correlated well with those absorbed by young wheat seedlings. The Ca-saturated Chelex membrane extractable Cd, Cu and Pb of the soil had the strongest correlation with plant uptake Cd, Cu and Pb among the extraction methods we tested. It was demonstrated that the Ca-saturated Chelex membrane extraction is an appropriate method in simultaneously estimating Cd, Cu and Pb phytoavailability of soil and is applicable to a wide range of soils.     

Effects of organic amendments on Cd, Zn and Cu bioavailability in soil with repeated phytoremediation by Sedum plumbizincicola

Organic materials with different functional groups can be used to enhance metal bioavailability. Traditional organic materials (rice straw and clover) and ethylenediamine disuccinic acid (EDDS) were applied to enhance metal uptake from polluted soil by Sedum plumbizincicola after repeated phytoextraction. Changes in pH, dissolved organic carbon (DOC) and metal concentrations were determined in the soil solution after EDDS application. Amendment of the soil with ground rice straw or ground clove resulted in higher concentrations of Cd only (by factors of 1.92 and 1.71 respectively) in S. plumbizincicola compared to control soil. Treatment with 3 mmol kg(-1) EDDS increased all the metals studied by factors of 60.4, 1.67, and 0.27 for Cu, Cd, and Zn, respectively. EDDS significantly increased soil solution DOC and pH and increased soil plant-available metals above the amounts that the plants could take up, resulting in high soil concentrations of soluble metals and high risk of ground water contamination. After repeated phytoremediation of metal contaminated soils the efficiency of metal removal declines as the concentrations of bioavailable metal fractions decline. Traditional organic materials can therefore be much more effective and environmentally friendly amendments than EDDS in enhancing phytoremediation efficiency of Cd contaminated soil     

The Development of a Phytoremediation Technique for the Detoxification of Soils Contaminated with Phenolic Compounds Using Horseradish Peroxidase (Armoracia rusticana): Preliminary Results

The proposed phytoremediation technique is based on the successful exploitation and optimization of oxidative coupling, mediated by horseradish peroxidase. Susceptibility to degradation of a selection of phenolic compounds, in solution, by horseradish peroxidase appears to be structurally related and was found to be of the order 2,4-dichlorophenol (2,4-DCP) > 4-chlorophenol (4-CP) > 2-chlorophenol (2-CP). Only 1.89% of 2,4-DCP, at an initial concentration of 5 mM, remained unchanged at the end of the experiment. Reaction rates between purified horseradish peroxidase and 2,4-DCP were found to be extremely rapid with 74% of the substrate removed from solution during the first 30 s. Inhibition of the reaction by the heavy metals Cd, Zn, Ni, and Pb at concentrations of 100 mg/l is of concern because these metals are often present in contaminated soils. H₂O₂ has a dominant role in optimizing peroxidase activity in crude horseradish extracts. Fluctuations in temperature and pH, normally experienced in soils, did not appear to have a detrimental impact on peroxidase activity. However, the functioning of the enzyme is seriously affected at a pH ≤ 3. All reactions in this study were carried out in solution.     

Experimental Assessment of Using Soluble Humic Substances for Remediation of Heavy Metal Polluted Soils

Since heavy metals are nondegradable and strongly bonded in soils, remediation of heavy metal polluted soils by extraction is difficult and current extraction techniques require harsh chemicals such as ethylenediaminetetraacetic acid (EDTA). However, use of EDTA is environmentally problematic because of costs, persistence, toxicity and deterioration of soil structure. Therefore, the potential of soluble natural humic substances (HS) to extract heavy metals from contaminated soils is tested as an environmentally friendly substitute for EDTA. A strongly polluted, calcareous urban soil (CRC soil) and a moderately polluted agricultural soil (CUP soil) were extracted at neutral pH in batch mode by three HS solutions from beech and Norway spruce litter (Beech-HS and Spruce-HS) and processed cow slurry (Bio-HS), all containing 25 mM dissolved organic carbon (DOC). After 10 extractions with a solution to soil ratio of 5:1 (L/kg), 8% to 39% of the total Cd, Cu, Ni and Pb soil contents, lowest for Ni and highest for Cu/Pb, were extracted. Natural and processed HS samples had comparable capacities to extract the heavy metals. A comparison of 100 mM DOC of Bio-HS and EDTA as extractants for Cu from the CRC soil showed extraction of 67% by EDTA and 41% by Bio-HS, indicating somewhat higher efficiency of EDTA than of HS. Sequential extraction of the CRC soil after Bio-HS and EDTA extraction showed removal of exchangeable, carbonate- and metal oxide-bound Cu but also of some residual Cu. It is therefore concluded that HS appears to be an attractive and promising alternative to EDTA as remediation agent for heavy metal polluted soils provided cheap HS of good quality is easily available.     

Chemical Extraction of Arsenic and Heavy Metals from Contaminated Soils Under High Temperature and Pressure Conditions in Abandoned Mines in South Korea

The chemical extraction of As and heavy metals from contaminated soils, sampled from the Geopoong and Keumpoong mines in South Korea, was investigated under subcritical conditions. Soil samples from the abandoned mines were heavily contaminated with As, Cd, Cu, Pb, and Zn. The extent of metal removed from the contaminated soils by extractants varied according to the chemical forms of the metals in the soils. When temperature increased, the extraction of As increased accordingly, showing 92-100% removal with 100 mM of NaOH at 300°C. In contrast, the extraction of cationic metals by citric acid and ethylenediaminetetraacetic acid (EDTA) decreased markedly at 200–300°C because their chelating ability was decreased via decarboxylation and dehydration at high temperatures. Furthermore, the extraction of cationic metals was significantly affected by solution pH. Our results suggest that chemical extraction of cationic metals under subcritical conditions may be affected by several factors, including character of metal, type of extracting reagent, existing forms of metal in the soil, temperature, and soil pH.     

Soil microbial activities and heavy metal mobility in long-term contaminated soils after addition of EDTA and EDDS

A 40-day incubation experiment was carried out in order to evaluate the microbial activities and heavy metal availability in long-term contaminated arable and grassland soils after addition of EDTA (ethylenediaminetetraacetic acid) or EDDS ([S,S]-ethylenediaminedisuccinic acid). Soils with similar contamination of heavy metal from the vicinity of a lead smelter were used in the experiment. The soil microbial carbon (C_mic) decreased significantly after addition of EDTA in the arable soil (CM1); lesser effects were observed in the grassland soil (CM2). Addition of EDDS caused a decrease of C_mic during the first 10 days of incubation. In the later phases of the experiment, C_mic increased, and even exceeded the amounts found in the control soils. Respiratory activities and metabolic quotients (qCO₂) increased after the addition of the chelating agents into the soils. Higher respiratory activities and qCO₂ were observed in the EDTA-treated soils. The readily available heavy metal fractions were extracted with NH₄NO₃ solution. Readily mobilizable heavy metal fractions of Cd, Pb, Zn, and (in part) Cu increased during the first 3-10 days of incubation in the presence of EDTA. The addition of EDDS particularly increased concentrations of available Cu. Significant correlations between NH₄NO₃-extractable metals, soil respiratory activities, and qCO₂ were found in both soil treatments with EDTA and EDDS. This indicates that enhanced metal mobility seriously affects the microbial processes in experimental soils. In addition, the relationships between NH₄NO₃-extractable Cd, Cu, and the microbial biomass were found in the CM1 soil amended with EDTA.     

2,4-二氯苯酚在土壤与河流底泥中降解动力学

以南京化学工业园内四柳河沿岸土壤与河流底泥为研究对象,通过土壤灭菌、温度与污染物初始浓度调控,研究了2,4-二氯苯酚在土壤与河流底泥中降解动力学及其影响因子。结果表明:微生物对2,4-二氯苯酚降解起主导作用,在45d内,非灭菌土壤和河流底泥的降解率分别是灭菌条件下的1.5～3倍、1.4～2.8倍,土壤和河流底泥中的2,4-二氯苯酚微生物降解量分别为0.128～0.599和0.113～0.718mg·kg-1,非灭菌处理半衰期时间短于灭菌处理;(10±1)℃～(30±1)℃范围内,随着温度的增高,2,4-二氯苯酚降解加快,在(30±1)℃土壤与河流底泥中残留量最小,分别为0.305和0.203mg·kg-1,半衰期也最短;土壤与河流底泥中的2,4-二氯苯酚均在其浓度为0.5mg·kg-1时降解最快,随着初始浓度的增加,2,4-二氯苯酚降解速度呈现递减趋势,半衰期增长。     

氰化物污染的植物修复可行性研究

氰化物是目前世界范围内最常使用的提取黄金和白银等贵重金属的沥滤剂,其对自然生态环境的污染和破坏以及对人畜和其它生物的毒性作用是众所周知的.本试验用一自行设计的生物反应器来观察黄豆(Glycine max(L)Merr.)和玉米(Zea mays L.)对氰化物污染土壤的原位修复的可能性.室温条件下(23.0～26.0℃),低浓度的氰化物污染液对(≤45.5 CN mg·L^-1)二种测试植物的生长没有产生任何毒性作用;而在高浓度的氰化物试验组(≥91.0 CNmg·L^-1),二种测试植物的生长都出现了明显的滞长现象(生长率下降大于10%),但没有观察到其它毒性反应.同时二种测试植物的叶片细胞用来测定植物细胞线粒体中的氰丙氨酸合成酶(β-cyanoalanine synthase)转化氰化物的潜力.实验是在一封闭的玻璃器皿(100mL)中进行的(100mL的氰化钾溶液中加入1.5g(鲜重)植物的叶片,氰化钾溶液的浓度大约1.0 CNmg·L^-1).在为期28 h的时间内,水溶液中超过90%的氰化物被植物的叶片去除;黄豆和玉米的的叶片细胞对氰化物去除率分别测定为4.43mg CN·kg^-1(鲜重)·h^-1和3.42mg CN·kg^-1(鲜重)·h^-1.本实验结果表明,植物对氰化物污染的土壤原位修复方法是一种可行的和有效的选择.     

Influence of Soil Organic Matter on Copper Extraction from Contaminated Soil

Column experiments of copper extraction from four contaminated soils characterized by a content of Soil Organic Matter (SOM) ranging from 1% to 25% are presented and discussed. The extraction was performed by flushing the soil with an aqueous solution of a sodium salt of ethylene diamminotetraacetic acid (EDTA). Preliminary tests were performed on a soil containing 25% of organic matter, to investigate the influence of pH, concentration and volumes of EDTA on its chelant action and on the dissolution of SOM. Having selected the optimal conditions for the extraction process, a further series of tests was conducted on the four soils to evaluate the influence of organic content on copper extraction yields. EDTA solutions at 0.01 M, 0.05 M, 0.1 and 0.2 M were injected at 0.33 ml/s; copper and organic matter extraction yield were determined. At a pH of 5, 15 pore volume (PV) of a solution containing 0.05M EDTA, extracted about 99% of copper contained by the soil with the higher organic matter content. Under the same conditions, and for soil with > 6% SOM, extraction yields over 80% were achieved, while at lower organic content, copper extraction was dramatically reduced. This was attributed to the formation of highly stable copper-humate complexes and to their increasingly dissolution that occurred in the soils with higher organic matter level.

Experimental tests performed at different contamination levels (1200 mg/kg, 2400 mg/kg) showed that EDTA extraction effectiveness also depended upon initial soil Cu concentration.     

Kinetic and isothermal studies on liquid-phase adsorption of 2,4-dichlorophenol by palm pith carbon

Adsorption studies were conducted to study the removal of 2,4-dichlorophenol (2,4-DCP) from aqueous solution on palm pith carbon under varying experimental conditions such as agitation time, adsorbent dose, pH and temperature. Higher 2,4-DCP was removed with decrease in the initial concentration of 2,4-DCP and increase in amount of adsorbent used. Kinetic study showed that the adsorption of 2,4-DCP on palm pith carbon was a gradual process. Adsorption capacities were 19.16 mg/g for the particle size of 250-500 microm. The equilibrium time was 60 and 80 min for 10 and 20 mg/L and 100 min for both 30 and 40 mg/L phenol concentrations, respectively. Acidic pH was favourable for the adsorption of 2,4-DCP. Studies on pH effect and desorption showed that chemisorption seemed to play a major role in the adsorption process. Thermodynamic study showed that adsorption of 2,4-DCP on palm pith carbon was more favoured. The change in entropy (DeltaS0) and heat of adsorption (DeltaH0) of palm pith carbon was estimated as 30.72 J/mol/k and 7.16 kJ/mol, respectively. The high positive value of change in Gibbs free energy indicated the feasible and spontaneous adsorption of 2,4-DCP on palm pith carbon. The results indicated that palm pith carbon was an attractive candidate for removing phenols from wastewater.     

Horseradish-Mediated Binding of 2,4-Dichlorophenol to Soil

Applying minced horseradish roots enhanced the binding of ¹⁴C-labeled 2,4-dichlorophenol (2,4-DCP) to soil. The presence of peroxides was necessary to activate the oxidation reactions mediated by peroxidases present in the plant tissues. The transformation of 2,4-DCP was completed in 30 min, and the extent of binding depended on the amount of horseradish added to the polluted soil, the concentration and type of peroxide applied as an electron acceptor, and the soil moisture. In reactions with H₂O₂, binding increased from 8 to 50% of the initial radioactivity as the amount of horseradish increased from 0 to 0.5 g per 5 g of soil when the soil was completely saturated with water. The rate of binding was enhanced by a factor of two when calcium peroxide was substituted for hydrogen peroxide. After extraction with water, less than 15% of the initial radioactivity was released from the horseradish-treated soil, compared with 90% released from the untreated control. Most of the radioactivity extracted from treated soil with 0.5 M sodium hydroxide (48%) was associated with humic and fulvic acids (34%). The results obtained provide clear evidence that horseradish treatment of soil polluted with chlorophenols may be an effective means of remediation.     

Perchlorate Remediation by Electrokinetic Extraction and Electrokinetic Injection of Substrates

Perchlorate (ClO₄^-) contamination of groundwater has recently become a major concern across the nation. Electrokinetic (EK) extraction with the simultaneous EK injection of organic material to promote degradation could allow for the efficient removal of perchlorate while simultaneously promoting degradation of perchlorate. Column experiments were conducted to evaluate the technology. Lactate and glycine served as organic substrates to promote degradation after injection into the columns as well as maintaining the pH near neutral. Removal of perchlorate from contaminated materials kaolin, sand, and a natural soil historically contaminated by perchlorate was controlled by the ionic flux of perchlorate and not by transport from the osmotic flux which was only significant for kaolin experiments. Perchlorate was removed from contaminated sand and clay below our detection limits (5 ppb). Both lactic acid and glycine were successfully injected into clay and a sand matrix. Results from a contaminated site soil indicate that the Chemical Oxygen Demand was increased after electrokinetic injection of glycine and lactate. Experiments using soil from a contaminated site confirmed that EK can be used to both remove perchlorate and stimulate bioremediation by the injection of lactate or glycine. The use of EK technology to both remove and provide for continued source removal by bioremediation offers a potential new tool to treat low permeability systems.     

Soil Washing Enhanced by Humic Substances and Biodegradable Chelating Agents

Industrial timber treatment sites have resulted in widespread soil contamination by Cu, Cr, and As, presenting potential long-term liability and associated risks to human health and the environment. This study evaluated the roles of natural humic substances (lignite-derived humic substances, standard and commercially available humic acids) and biodegradable chelating agents (ethylenediamine-N,N-disuccinic acid (EDDS) and glutamic-N,N-diacetic acid (GLDA)) for soil washing. Batch kinetic experiments revealed that humic substances promoted Cu extraction at pH 8, but they were significantly adsorbed on the soil at pH 4, possibly posing impediment to soil remediation. The metal extraction by EDDS and GLDA was comparable to that of EDTA (ethylenediamine-tetraacetic acid), and it was more effective at pH 4 than pH 8, probably due to acidic dissolution of metal precipitates and oxides. Metal distribution analysis indicated that the carbonate fraction of Cu and the oxide fraction of As and Cr were mainly extracted, while the exchangeable fraction of Cu increased. The residual leachability tests showed that humic substances reduced the Cu and As leachability but the reduction was insufficient. In contrast, EDDS was able to reduce the leachate concentrations of Cu and As to below 5 mg L^?1, meeting the waste acceptance criteria for landfill disposal. Nevertheless, soil washing methods and remediation strategy may need further modifications to facilitate site restoration and promote soil recycling.     

An investigation of the anion-exchange resin method for soil phosphate extraction

Summary The anion-exchange resin method for soil-phosphate extraction was investigated on 4 different soils under varying experimental conditions. The variables were: (a) the type of anion-exchange resin, (b) the anionic form of the resin, (c) the ratio between the amounts of resin, soil, and water, and (d) the time of shaking. The amount of P extracted was dependent on the anionic form of the resin. For resins in the chloride form both the amount of P extracted psr soil unit and the pH of the soil suspension varied with the type of resin and the soil-water ratio. Resins in the bicarbonate form stabilized the system, so that the amount of P extracted and the suspension pH were almost independent of the type of resin and the soil-water ratio. The results indicated that the rate-determining step in the overall process of P transport from the soil phase through the water phase to the resin phase is the P desorption from the soil phase to the water phase, provided the resin is added in excess. The rate of this P desorption is dependent on the chemical composition of the water phase, which in turn is governed by the type of soil, the soil-water ratio, the time of shaking and the anionic form of the resin. In a final experiment a resin was used in the chloride- and the bicarbonate form, respectively, for extraction of phosphate from 34 soils. The available P of these soils had been determined 15 years before in a pot experiment with ryegrass and by different laboratory methods². The degree of correlation between the ryegrass P uptake and the P. determined by the laboratory methods decreased according to the following order: resin (bicarbonate form), resin (chloride form), 0.5M sodium bicarbonate, L value, E value, ammonium lactate solution, sodium zeolite, 0.01M calcium chloride, phosphate potential, and 0.1M sulphuric acid. It is recommended that resins in the bicarbonate form should be used for both routine as well as more advanced analyses of the ability of soils to supply phosphate to plants. A final procedure for the analysis is given in the paper.     

Influence of [S, S]-EDDS on phytoextraction of copper and zinc by Elsholtzia splendens from metal-contaminated soil

Two pot experiments were conducted to investigate the time course effects of the (S, S)-N, N'-ethylenediamine disuccinic acid (EDDS) addition to contaminated soil on the uptake of Cu and Zn by the Cu accumulator Elsholtzia splendens and on plant Cu and Zn concentrations at different growth stages. EDDS increased the amounts of Cu and Zn soluble in the soil, taken up by plants, concentrated in the xylem sap, and translocated from roots to stems and leaves. The increase in soil-soluble metals, especially Cu, resulted in a corresponding increase in metal concentrations in the xylem sap and leaves. The addition of EDDS to the soil increased plant Cu and Zn concentrations, especially in the leaves, and changed the proportions of Cu and Zn taken up by different plant parts. The proportions of Cu and Zn taken up by the roots were higher than by the leaves of control plants, but EDDS-treated plants showed the opposite trend. EDDS exerted greater effects at the end of the vegetative growth stage than at the start of the flowering or reproductive stages.     

Plant uptake and the leaching of metals during the hot EDDS-enhanced phytoextraction process

Using pot experiments, the effect of the application of the biodegradable chelating agent S,S-ethylenediaminedisuccinic acid (EDDS) in hot solutions at 90 degrees C on the uptake of Cu, Pb, Zn, and Cd by corn (Zea mays L. cv. Nongda No. 108) and beans (P vulgaris L. white bean), and the potential leaching of metals from soil, were studied. When EDDS was applied as a hot solution at the rate of 1 mmol kg(-1), the concentrations and total phytoextraction of metals in plant shoots exceeded or approximated those in the shoots of plants treated with normal EDDS at the rate of 5 mmol kg(-1). On the other hand, the leaching of Cu, Pb, Zn, and Cd after the application of the hot EDDS solution at the rate of 1 mmol kg(-1) was reduced by 46%, 21%, 57%, and 35% in comparison with that from the application of normal EDDS at 5 mmol kg(-1), respectively. For treatment with 1 mmol kg(-1) of EDDS, the leached metals decreased to the levels of the control group (that without EDDS amendment) 14 d after the application of EDDS. The soil amendment with biodegradable EDDS in hot solutions may provide a good alternative to chelate-enhanced phytoextraction in enhancing metal uptake by plants and limiting metals from leaching out of the soil.     

可降解螯合剂对镉胁迫下籽粒苋根系形态及生理生化特征的影响

采用盆栽试验研究了可降解螯合剂EDDS和NTA对镉胁迫下籽粒苋(Amaranthus hybridus L.)根系形态及生理生化特征的影响。结果表明:当螯合剂施入10 mg/kg的镉污染土壤后,籽粒苋根系生物量和总长等根系形态指标与对照无显著差异,过氧化物酶(POD)、过氧化氢酶(CAT)活性、谷胱甘肽(GSH)和可溶性蛋白含量显著上升。当螯合剂施入100 mg/kg的镉污染土壤后,籽粒苋根系生物量、总长、表面积、体积及侧根数比对照显著减少了12.30%—23.98%、17.01%—24.90%、41.87%—57.93%、16.46%—32.94%和23.48%—53.35%;EDDS的施入使籽粒苋根系POD、CAT活性、GSH和可溶性蛋白含量显著升高;而NTA施入后,根系中的POD活性比对照降低了4.12%—35.95%,并且CAT活性和可溶性蛋白含量在2 mmol/kg NTA处理下分别显著降低了14.66%—15.79%和26.81%—30.48%;EDDS和NTA施入后,GSH含量比对照显著升高了14.73%—65.65%和28.05%—84.10%。当镉处理浓度分别为10 mg/kg和100 mg/kg时,螯合剂的施入显著增强了籽粒苋根系对镉的吸收,比对照分别增加了40.76%—103.10%和15.03%—49.49%。因此,EDDS和NTA施入镉污染土壤后,通过影响籽粒苋根系形态和生理生化过程以响应重金属镉的胁迫。