南通市环境信访现状分析及对策

环境问题是当今国际社会普遍关注的问题，在中国尤为突出。由于特殊的国情，中国的环境问题呈现出与众不同的状况，因此，环境信访形势也显得十分严峻。现以南通市为例，从环境信访现状、成因等方面阐述了加强信访督查力度的对策，并对做好信访工作提出了一些合理的建议。     

欠发达地区环境信访演变特点及对策思考

以射阳县为例,阐述了欠发达地区环境信访的特点,分析了环境投诉增多的原因,从落实科学发展观、构建和谐社会的高度,提出了具体对策。     

杭州市中心城区环保信访分析

群众信访是公众参与环境监督的途径之一，是公民环境意识和自我保护意识提高的重要标志。居民享有高质量生活环境的权利，企业有实现自身利益最大化的愿望，两者权力的界定和环境资源的配置依靠政府环保部门严格按照国家环保法律法规予以保障。但实际情况是企业为追求利润最大化往往牺牲外部环境，给周围居民日常生活带来影响。以杭州市中心城区下城区为例，１９９８年度共收到反映环境问题的来信来访来电２７０件，比１９９７年增长１８％。１下城区概况及环保信访下城区地处杭州市区中心，濒临美丽的西子湖，经济繁荣、商贸发达、交通便利…     

大学环境教育与环境建设

从中国生态环境的现状和大学传授学生知识、确立学生观念的特殊地位说明了在高校进行环境教育的必要性。环境教育是让学生了解人类生活和文明发展历程中的环境状况和问题，思考环境保护的意义和价值，进而确立环境观念。提出了建设环境友好型大学。建议在高校中建立讲座、选修、必修三位一体的环境教育教学体系。     

初始环境评审中环境因素的识别和评价方法

初始环境评审是组织建立和实施环境管理体系的基础，而环境因素的识别和评价是这一过程的关键。探讨了识别和评价环境因素的准则，介绍了几种环境因素的识别和评价方法。     

环境保护的哲学思考

阐述了环境工作的哲学属性，对所谓环境工作(包括环保工作)认为就是遵循客观规律，主要是自然规律和市场经济规律，综合运用行政的、经济的、法律的、教育的、技术的等手段，主要是运用经济的和法律的手段，调节环境与发展之间的关系，促使其间的矛盾由“两难”向“双赢”转化，不断在更高层次上寻求环境与发展的相对统一，为环境和经济、社会的可持续发展作出贡献。     

宜兴市环境地理信息系统研究与应用

环境地理信息系统是环境保护管理和决策的现代化工具，它的发展将为环境保护事业带来巨大的影响。作者以宜兴市为实例，详细介绍了环境地理信息系统的系统概况、数据库的设计以及系统的功能和环境地理信息系统的重要性。     

公路沿线环境与交通安全

随着改革开放和国家经济的不断发展，交通事业腾步起飞，浙江省目前已经拥有了高速公路158km，一级公路189km，二级公路2885km。公路的发展带动了公路沿线的经济发展，同时也带来了一系列的环境问题，其中公路沿线的交通安全问题被世界银行贷款项目视为最重要的社会环境问题。目前除了高速公路是全封闭全立交外，一级和二级公路一般还是以局部封闭和平交为多，沿线的环境复杂，交通事故频发。文章以世界银行贷款的32O国道嘉兴辖区交通安全工程为例，对沿线的环境、交通量及交通事故等调查资料进行分析，认为公路沿线的交通事故的引发是多种…     

环境标准实际执行中的存在问题

从规范环境管理和环境执法出发，结合其实际执行过程使用环境标准存在的问题作了简单归纳，并提出初步建议。     

环境费税研究现状与展望

环境费税是环境保护经济手段的重要组成部分，对于控制污染、实现环境与经济的协调和可持续发展具有重要的意义。文章概述了环境费税研究的现状，并展望了未来发展的趋势。     

Sorption and desorption of Cu and Cd by macroalgae and microalgae

The sorption and desorption of Cu and Cd by two species of brown macroalgae and five species of microalgae were studied. The two brown macroalgae, Laminaria japonica and Sargassum kjellmanianum, were found to have high capacities at pHs between 4.0 and 5.0 while for microalgae, optimum pH lay at 6.7. The presence of other cations in solution was found to reduce the sorption of the target cation, suggesting a competition for sorption sites on organisms. Sorption isotherms obeyed the Freundlich equation, suggesting involvement of a multiplicity of mechanisms and sorption sites. For the microalgae tested, Spirulina platensis had the highest capacity for Cd, followed by Nannochloropsis oculata, Phaeodactylum tricornutum, Platymonas cordifolia and Chaetoceros minutissimus. The reversibility of metal sorption by macroalgae was examined and the results show that both HCl and EDTA solutions were very effective in desorbing sorbed metal ions from macroalgae, with up to 99.5% of metals being recovered. The regenerated biomass showed undiminished sorption performance for the two metals studied, suggesting the potential of such material for use in water and wastewater treatment.     

Kinetic and structural relationships of transition monomeric and oligomeric carboxyl- and choline-esterases

The kinetic and structural relationships of eight electrophoretically pure mammalian serum and liver serine carboxylesterases (CE) and cholinesterases (ChE) have been studied. Eight CE's and ChE's, which were fully resolved but only partially purified, provided additional information. Five of the electrophoretically pure esterases were monomeric, and of these, four belonged to a new and widely distributed class. These four monomeric esterases hydrolyzed choline esters, but at widely differing rates. Thus two were termed monomeric butyrylcholinesterases, mBuChE I and II, and two were monomeric CE's (mCE). The rabbit liver mCE was not a subunit of the oligomeric CE (oCE), although the oCE also hydrolyzed choline esters at a very low rate. The complex kinetics of the mCE's, mBuChE's, oCE's, and of the oligomeric BuChE's of horse and human serum could be interpreted according to a single reaction scheme involving an allosteric site and the equation derived from it. Thus activation and inhibition at high substrate concentrations, together with sigmoidal activity versus substrate concentration plots, all of which characterize the reactions of these esterases, could be interpreted by a single scheme and equation. Structural and kinetic comparisons showed a progressive transition of properties from the oCE's through the mCE's to the oBuChE's. One of the purified mCE's was from horse serum, and it exhibited physical and kinetic properties unlike those of the liver mCE's or oCE's.     

Persistence and dissipation kinetics of trifloxystrobin and tebuconazole in onion and soil

The persistence and dissipation kinetics of trifloxystrobin and tebuconazole on onion were studied after application of their combination formulation at a standard and double dose of 75 + 150 and 150 + 300 g a.i. ha^?1. The fungicides were extracted with acetone, cleaned-up using activated charcoal (trifloxystrobin) and neutral alumina (tebuconazole). Analysis was carried out by gas chromatograph (GC) and confirmed by gas chromatograph mass spectrometry (GC-MS). The recovery was above 80% and limit of quantification (LOQ) 0.05 mg kg^?1 for both fungicides. Initial residue deposits of trifloxystrobin were 0.68 and 1.01 mg kg^?1 and tebuconazole 0.673 and 1.95 mg kg^?1 from standard and double dose treatments, respectively. Dissipation of the fungicides followed first-order kinetics and the half life of degradation was 6–6.6 days. Matured onion bulb (and field soil) harvested after 30 days was free from fungicide residues. These findings suggest recommended safe pre-harvest interval (PHI) of 14 and 25 days for spring onion consumption after treatment of Nativo 75 WG at the standard and double doses, respectively. Matured onion bulbs at harvest were free from fungicide residues.     

Sorption and desorption behavior of chloroanilines and chlorophenols on montmorillonite and kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.     

Sorption and Desorption Behavior of Chloroanilines and Chlorophenols on Montmorillonite and Kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.     

Bacterial and archaeal diversity in oil fields and reservoirs and their potential role in hydrocarbon recovery and bioprospecting

Environmental Science and Pollution Research - Hydrocarbon is a primary source of energy in the current urbanized society. Considering the increasing demand, worldwide oil productions are declining...     

畜禽养殖业污染与循环经济

解决畜禽养殖业的污染问题要以充分利用资源为根本出发点，通过对污染全过程控制及废物综合利用，达到畜禽粪便的减量化、无害化、资源化，走循环经济的发展道路。     

Synthesis and characterization of m- and p-methylbenzyl-mercapturic acids derived from m- and p-xylenes

Chemical synthesis and physical properties of two mercapturic acids suggested as urinary metabolites of m- and p-xylenes ace described. These compounds may be used for the identification and quantivative determination by high-performance liquid chromatography of the corresponding mercapturic acids in urine.     

Sources and fate of PCDD and PCDF

PCDD and PCDF were found in urban air particulates from St. Louis and Washington, D.C., and in sediments from the Great Lakes and Siskiwit Lake, Isle Royale. The similarity between the PCDD and PCDF found in air particulates and sediment samples and the presence of PCDD and PCDF in sediment from Siskiwit Lake (a location which can receive only atmospheric inputs) suggest that these compounds are emitted to the atmosphere from combustion sources. The historical input of PCDD and PCDF to dated sediment cores shows a strong increase since 1940, and this suggests that the incineration of chlorinated organic compounds is an important source of PCDD and PCDF to the environment.