芜湖市郊土壤污染对土壤动物群落结构的影响

研究表明，芜湖市郊农田土壤动物群落的组成与数量随污染程度的加重而减少，土壤动物密度也呈同样的变化趋势，特别是中小型土壤动物，优势类群数量发生较大消长，常见类群和稀有类群的组成逐渐减少．多样性指数H与重金属污染程度之间关系因受到季节的影响而变得复杂：冬季和初夏污染较重样地优势类群数量减少，群落均匀性指数E增加而优势度指数C减小，多样性指数H较高；而春季处于过渡阶段，某些类群(如螨类)数量爆发，C增高，H较小．土壤动物群落密度一类群指数DG随污染加重而减小．受到重金属污染的农田土壤动物的表聚性减弱，甚至出现逆分布现象．图1表4参15     

新构造运动对安徽土壤分布的影响

安徽地跨亚热带与温带,过渡性特征明显,境内有山地,丘陵和平原,自然地理景观复杂多样,各区域由于所处大地构造单元不同,其新构造运动的表现形式也不同,它制约着区域地貌的发育,成土母质类型和地面气候状况,从而影响了该区域土壤的分布特征。     

几种螯合剂对污染土壤的重金属提取效率的研究

在Cd,Pb污染的土壤上,采用批提取实验(batchexperiment),研究了几种螯合剂和不同的水土比对重金属提取效率的影响。结果表明:螯合剂对Cd的提取效率随着各淋洗剂浓度的提高而逐渐提高,相同浓度下各淋洗剂的提取效率大小顺序依次为EDTA>DTPA>NTA>PA>CA>CD>HCl。随水土比提高,相应的提取效率也提高。几种淋洗剂中只有EDTA对Pb和Cd都能达到理想的淋洗效果。     

淮安市绿色食品生产基地环境质量研究

绿色食品的产地，必须达到一定的环境质量标准，故生产基地环境质量研究是生产绿色食品的关键。主要环境要素有：土壤、水质、大气环境以及绿色食品基地现产食品中农药残留量。     

Phytoremediation and its models for organic contaminated soils

Soil pollution has been attracting considerable public attentions over the last decades.Sorts of traditional physiochemical methods have been used to remove th organic pollutants from soils.However,the enormous costs and low efficiencies associated with these remediation technologies limit their availabilities.Phytoremediation is an emerging technology that uses plants to cleanup pollutants in soils.As overwhelmingly positive results have been shown,phytoremediation is a most economical and effective remediation technique for organic contaminated soils.In this paper phytoremediation and its models for organic contaminated soils are viewed.The mechanisms of phytoremediation mainly include the direct plant uptake of organic pollutants,degradation by plant-derived degradative enzymes,and stimulated biodegradation in plat rhizosphere.Phytoremediation efficiency is close related to physicochemical properties of organic pollutants, environmental characteristics,and plant types.It is no doubt that soil amendments such as surfactants improve the solubilities and availabilities of organic pollutants in soils.However,little information is available about effects of soil amendments on phytoremediation efficiencies.Phytoremediation models have been developed to imulate and predict the environmental behavior of organic pollutants,and progress of models is illustrated.In many ways phytoremediation is still in its initial stage,and recommendations for the future for the future research on phytoremediation are presented.     

再生铅冶炼对土壤环境影响及其评价和环境管理

再生铅冶炼是对废弃物的循环利用,防治铅污染的重要手段,但冶炼中处置不当,会引起土壤污染,再生铅冶炼对土壤环境的影响,首先进行环境影响识别,并根据冶炼中铅的排放强度和铅的生物地球化学循环规律来阐明其排放特点和进入土壤的途径,通过再生铅冶炼项目环境影响评价的实例,探讨了土壤环境质量的现状分析、评价和预测等研究方法,并提出严格执行环境影响评价制度和“三同时”制度,强化建设项目本身的环境管理和完善土壤环境质量标准等土壤环境管理措施。     

不同土地利用类型下土壤特性及重金属评价

在哈尔滨市周家镇选择典型的五种土地利用类型(耕地、居民点及工矿用地、交通用地、林地、水域),24个样品,研究乡级小城镇不同土地利用类型下土壤特性及重金属状况.结果显示:(1)耕地的土壤理化性状最低,有机质与全氮有显著的正相关;(2)乡级小城镇不同土地利用类型下土壤中Zn、Pb含量存在显著差异,交通用地与耕地含量较高,同时各土地利用类型的内梅罗综合污染指数均达到中污染;(3)人类活动对土壤质量影响最大的是交通活动,其次是耕地施肥、使用农药及翻耕等,在次是居民生活.     

Adsorption of chloroacetanilide herbicides on soil and its components Ⅲ. Influence of clay acidity, humic acid coating and herbicide structure on acetanilide herbicide adsorption on homoionic clays

Adsorption of chloroacetanilide herbicides on homoionic montmorillonite, soil humic acid, and their mixtures was studied by coupling batch equilibration and FT-IR analysis. Adsorption isotherms of acetochlor, alachlor, metolachlor and propachlor on Ca²⁺-, Mg²⁺ -. Al³⁺ -and Fe³⁺ -saturated clays were well described by the Freundlich equation. Regardless of the type of exchange cations, Kf decreased in the order of metolachlor ＞ acetolachlor ＞ alachlor ＞ propachlor on the same clay. FT-IR spectra showed that the carbonyl group of the herbicide molecule was involved in binding, probably via H-bond with water molecules in the clay interlayer. The type and position of substitutions around the carbonyl group may have affected the electronegativity of oxygen, thus influencing the relative adsorption of these herbicides. For the same herbicide, adsorption on clay increased in the order of Mg²⁺ ＜ Ca²⁺ ＜ Al³⁺ ≤ Fe³⁺ which coincided with the iucreasing aciditv of homoionic clays. Acidity of cations may have affected the protonation of water, and thus the strength of H-bond between the clay water and herbicide. Complexation of clay and humic acid resulted in less adsorption than that expected from independent adsorption by the individual constituents. The effect varied with herbicides, but the greatest decrease in adsorption occurred at a 60:40 clay-to-humic acid ratio for all the herbicides. Causes for the decreased adsorption need to be characterized to better understand adsorption mechanisms and predict adsorption from soil compositions.     

14C-甲磺隆在土壤中的可提态残留、结合态残留和矿化

在实验室培养条件下,从质量平衡角度,研究了14C-甲磺隆在7种土壤中形成结合残留(14C-BR)、可提态残留(14C-ER)以及矿化为14CO2的规律;同时对14C-BR的主要影响因子及其在腐殖质中的分布规律进行了研究.结果表明:①14C-甲磺隆在土壤中形成的14C-ER,其含量与土壤pH呈显著正相关.甲磺隆母体化合物在7种土壤中 的半减期为13.3～66.6d,降解速率常数λ(d-1)与pH呈显著负相关.②14C-甲磺隆在7种土壤中形成的14C-BR,其含量在培养初期的20d内,与土壤pH呈显著负相关且与土壤粘粒含量呈显著正相关;而培养20d后,14C-BR的含量只与土壤pH呈显著负相关.pH是04C-甲磺隆在土壤中形成BR的主要影响因子.14C-甲磺隆在7种土壤中的14C-BR的最大值约为引入量的19.3%～52.6%.③在整个培养试验过程中,7种土壤中的14C-BR主要分布在富啡酸和胡敏素中,但其分布在胡敏酸中的相对百分比较小.因此,在14C-甲磺隆形成BR的过程中,富啡酸的作用＞胡敏素>胡敏酸.④在整个培养试验期间(180d),14C-甲磺隆在7种土壤中通过三嗪杂环开环矿化为14CO2的量约占引入量的12.9%～27.0%,其在碱性土壤中更难被矿化为14CO2.     

Speciation and fractionation of heavy metals in soil experimentally contaminated with Pb,Cd, Cu and Zn together and effects on soil negative surface charge

Speciation and fractionation of heavy metals in soil subsamples experimentally loaded with Pb, Cd, Cu and Zn in orthogonal design was investigated by sequential extraction, and operationally defined as water-soluble and exchangeable(SE), weakly specific adsorbed( WSA),Fe and Mn oxides-bound(OX) and organic-bound( ORG). The results showed that fractions of heavy metals in the soil subsamples depended on their speciation. About 90% of Cd and 75% of Zn existed in soil subsamples in the SE fraction. Lead and Cu existed in soil subsamples as SE, WSA and OX fractions simultaneously, although SE was still the major fraction. Organic-bound heavy metals were not clearly apparent in all the soil subsamples. The concentration of some heavy metal fractions in soil subsamples showed the good correlation with ionic impulsion of soil, especially for the SE fraction. Continuous saturation of soil subsamples with 0.20 mol/L NH4CI, which is the first step for determination of the negative surface charge of soil by the ion retention method, resulted in desorption of certain heavy metals from the soil. It was found that the percentage desorption of heavy metals from soil subsamples depended greatly on pH, the composition and original heavy metal content of the soil subsamples. However, most of the heavy metals in the soil subsamples were still be retained after multiple saturation. Compared with the parent soil, the negative surface charge of soil subsamples loaded with heavy metals did not show difference significantly from that of the parent one by statistical analysis. Heavy metals existed in the soil subsamples mainly as exchangeable and precipitated simultaneously.