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。     

厦门港表层水体中有机氯农药和多氯联苯的研究

利用ＧＣ－ＥＣＤ对厦门西港１９９８年７月取得上位表层水体中的１８种有机氯农药（ＨＣＨｓ，ＤＤＴｓ等）和１２种多氯联苯（ＰＣＢｓ）进行分析。其中有机氯农药的浓度范围６．６０～３２．６ｎｇ／Ｌ（其中ＨＣＨｓ：３．５１～２７．８ｎｇ／Ｌ），ｎｇ／Ｌ，ＤＤＴｓ，０．９５～２．２５ｎｇ／Ｌ均值１．４５ｎｇ／Ｌ），多氯联苯的浓度为０．０８～１．６９ｎｇ／Ｌ，同国内外其他港口海区相比较，其污染和蔼相对较低。同时     

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.     

珠江口水、沉积物及水生动物中氯苯类有机物的含量及分布

对珠江口水、沉积物及水生动物体内氯苯类有机物(CBs)的污染现状进行了调查,并对该类污染物在水体多介质体系中的转移分配规律进行了初步研究1.结果表明,珠江口表层水中CBs的总浓度为16.44～963.20ng·L-,DCBs(二氯苯)对污染的贡献较为突出,占74.4%;表层沉积物(干重)中CBs总含量为7.83～40.09 ng·g-1,DCBs、TCBs(三氯苯)、TeCBs(四氯苯)、PeCB(五氯苯)和HCB(六氯苯)分别占总量的71.4%、11.1%、13.0%、1.2%、3.6%;水生动物中贝类的CBs平均含量是38873.0ng·g-1、鱼类为2360.3ng·g-1、虾类则为565.0ng·g-1,DCBs和TeCBs是水生动物体内的主要污染物.CBs在水、沉积物及生物体之间存在明显的富集和放大作用.     

上海南汇潮滩表层中多环芳烃分布特征及环境意义

利用ＧＣ／ＭＳ分析了上海南汇淤泥质潮滩６，８两月表层沉积物中有机污染物多环芳烃，结果表明，该区在６月和８月８潮滩中ＰＡＨ组化芘，苯并芘及黄蒽具有较高的含量，并且在ＰＡＨ总量中所占比重也产大，在潮滩沉积物中已呈明显富集的趋势。     

公路边土壤和水稻中铅的分布,累积及临界含量

在距公路５、１０、５０、１００、２００ｍ准备收割的稻田中同时采集土壤及稻米样品。对２条公路的样品分析结果表明，汽车尾气中铅的污染大多集中在公路两侧５０ｍ左右的范围内。土壤自身性质对路边土壤及水稻中铅的分布、累积具有显著影响。经壤水稻中铅的累积量小于重壤水稻土，但轻壤水稻糙米的含铅量却高于重壤。轻壤中土壤含铅量和糙米含铅量之间具有相关关系。探讨了公路边土壤的临界含量问题，推算出轻壤中此值为５８ｍｇ／     

镉铅在粘土上的吸附及受腐殖酸的影响

试验研究了镉和铅2种重金属在蒙脱土和高岭土上的吸附,以及外加腐殖酸的3种组分（富里酸、棕色胡敏酸和灰色胡敏酸）的影响。镉铅在粘土上的吸附随着介质pH的升高而增加。在pH4-8范围内的任意pH点,镉在高岭土上的吸附量因富里酸而降低,因2种胡敏酸而升高;当pH值高于6时,吸附量急剧增加。外加富里酸使得铅在粘土上的吸附在pH＞6时意外出现随着介质pH而降低的趋势。     

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.