不同密度沉水植物腐解过程中水体DOM变化特征

选取白洋淀淀区的泥、水以及晒干的优势沉水植物金鱼藻、轮藻为研究对象,设置6个密度梯度模拟实验,分别于实验进行的50 d和100 d采集水样,运用紫外和荧光光谱技术研究沉水植物腐解阶段水体中溶解性有机质(DOM)的变化。结果显示,同步荧光光谱中,类蛋白峰荧光强度的变化不具规律性,类腐殖质峰荧光强度随密度的增加呈上升趋势,I2/I1的值随着密度的增加或时间的推移均逐渐增大;三维荧光光谱中,随着密度的增加,类富里酸荧光峰A和C的强度逐渐增加,而类色氨酸荧光峰T1的强度变化不大,腐解植物的密度大于3 kg/m3时各组均产生了类海洋腐殖质荧光峰B且强度随密度的增加逐渐增强,C峰的强度与水样中的COD和TP呈显著正相关;紫外光谱测定中,A253/A203的值随着密度的增加或时间的推移而逐渐增大,水体中的芳香族化合物也增多。     

Stable isotope on the evaluation of water quality in the presence of WWTPs in rivers

Environmental Science and Pollution Research - We investigated the distribution of nitrogen compounds in Han River as well as two tributaries of Tancheon and Jungrangcheon. Particularly, we...     

Evidence of differences in the biotransformation of organic contaminants in three species of freshwater invertebrates

Acute static bioassays were performed using three freshwater invertebrate species (the oligochaete Lumbriculus variegatus, the fingernail clam Sphaerium corneum and the larvae Chironomus riparius) exposed separately to a variety of 14C radiolabelled contaminants. The aim of this work was to investigate if the chemicals remained as parent compounds after the treatments. Chemicals used were 2,4-dichlorophenol; 2,4,5-trichlorophenol; pentachlorophenol; pyrene; Fenpropidin, and Trifluralin. Homogenates of the whole body tissue of each organism were prepared and total radioactivity was measured. Contaminants were then extracted into organic solvents and analysed by high-pressure liquid chromatography techniques. Chromatograms showed that most of the substances extracted were present as parent compounds in S. corneum and in L. variegatus. In contrast, for C. riparius a low proportion of the chemicals was recovered as parent compounds. These results suggest that different metabolic processes could take place in the different species.     

Quantification of nitrogen in the liquid fraction and in vitro assessment of lysine bioavailability in the solid fraction of soybean meal hydrolysates

Soybean meal (SBM) is a product generated from the manufacture of soybean oil and has the potential for use as a source of fermentable sugars for ethanol production or as a protein source for animal feeds. Knowing the levels of nitrogen available from ammonium is a necessary element of the ethanolic fermentation process while identifying the levels of essential amino acids such as lysine is important in determining usage as a feed source. As such the purpose of this study was to quantify total nitrogen and ammonium in the liquid fraction of hydrolyzed SBM and to evaluate total and bioavailable lysine in the solid fraction of the hydrolyzed SBM. The effects of acid concentration, cellulase and β-glucosidase on total and ammonium nitrogen were studied with analysis indicating that higher acid concentrations increased nitrogen compounds with ammonium concentrations ranging from 0.20 to 1.24 g L^?1 while enzymatic treatments did not significantly increase nitrogen levels. Total and bioavailable lysine was quantified by use of an auxotrophic gfpmut3 E.coli whole-cell bioassay organism incapable of lysine biosynthesis. Acid and enzymatic treatments were applied with lysine bioavailability increasing from a base of 82% for untreated SBM to up to 97%. Our results demonstrated that SBM has the potential to serve in ethanolic fermentation and as an optimal source essential amino acid lysine.     

Data ranges in aquatic toxicity of chemicals

A significant problem for effect assessment of aquatic ecosystems arises from the large ranges of toxicity data, which can be found in different databases and literature. Here, ranges are given for the aquatic toxicity of 27 high production volume chemicals. Based on these illustrative examples and on the current literature on uncertainty in aquatic effect assessment, toxicity ranges are discussed for their possible causes (variation in experimental condition, species, endpoint, time) and ways to handle them (safety factors). Implications and recommendations on the procedure of risk analysis of chemical substances are drawn. Two main requirements for a comprehensive risk assessment are identified, which often play a minor role in current practice (as they are often neglected) as well as in scientific discussion (as they are meant to be trivial). First, data quality must be checked critically before applying any result of a toxicity test. Secondly, experimental data should take into account different species and acute as well as chronic data. If these aspects are considered in risk analysis, which is common practice in ecotoxicology but not always in the context of practical applications in risk engineering, a more comprehensive picture of the environmental toxicity of a chemical substance can be obtained.     

The logistics of public participation in environmental assessment

This paper starts by investigating the rationales for public participation in environmental assessment. It is contended that access to participation may refer both to means as well as ends; thus, some advocates of citizen participation favour involvement for social and or political reasons (i.e. the participation is the end in itself). However, the value of that participation may also, as we shall see, advance quality and depth of knowledge (i.e. the participation is viewed only as a means to an end). The initial two sections, therefore, paint two broad brushstrokes: the first concerns why we should require public participation, and the second why that participation may improve the quality of our environmental assessment procedure. Further, it is then argued that the issues and problems of public participation vary across different environmental issues and also vary across different stages of the environmental assessment procedure and according to the scientific disciplines and practices involved. This paper points the way towards an open and representative style in which communities are included in environment assessment processes as a source of new or better knowledge, as well as a contribution towards what the EU refers to as the 'horizontal participatory approach'. The paper briefly considers methodological issues concerning ways in which participation might be carried out.     

Evaluation of dioxin-like chemicals in pooled human milk samples collected in Australia

DESIGN: Human milk samples were collected and analysed for the levels of polychlorinated dibenzodioxins (PCDDs), polychlorinated dibenzofurans (PCDFs) and selected dioxin-like polychlorinated biphenyls (PCBs). In total, 157 individual samples collected during 2002 and 2003 as well as 24 samples collected in 1993 were analysed as 20 pools. RESULTS: PCDDs, PCDFs and dioxin-like PCBs were detected in all pooled samples. For samples collected during 2002/2003, the TEQ(DFP) ranged from 6.0 to 15.2 pg TEQ g(-1) lipid with an average of 9.0 pg TEQ g(-1) lipid. The average lipid content was 3.7+/-0.5%. No systematic differences were observed in the levels of PCDDs, PCDFs and PCBs in human milk samples collected from different regions of Australia during 2002/2003. For samples collected in 1993 and analysed as pools, the mean level, expressed as TEQ(DFP) was 16+/-1.4 pg TEQ g(-1) lipid. The average lipid content was 3.9+/-0.7%. CONCLUSION: The levels of PCDDs, PCDFs and dioxin-like PCBs in the human milk of Australian women are both low compared to international levels and similar across all regions of Australia. Consistent with world-wide trends, the levels of PCDDs, PCDFs and dioxin-like PCBs have decreased over a 10 year period from 1993 to 2003 by approximately 40%.     

Risk assessment of heavy metals in suspended particulate matter in a typical urban river

Environmental Science and Pollution Research - Suspended particulate matter (SPM) is a major source of contamination in urban rivers as it serves as a carrier for pollutants, such as heavy metals....     

湖岸缓冲带反硝化作用的研究进展

反硝化作用是湖岸缓冲带去除硝酸盐的重要途径。湖岸缓冲带是联系陆地与湖泊生态系的纽带，不仅为许多动植物提供适宜生境，而且通过反硝化作用能去除地下水中的硝酸盐，提高湖泊水质。概述不同检测反硝化速率的方法，并对比各种方法的优点与缺点。阐述反硝化作用的影响因素：厌氧环境、有机碳、湖岸坡度、缓冲带坡度、pH与温度、硝酸盐浓度。介绍反硝化速率模型的研究开发状况。最后，提出了目前国内外反硝化研究中存在的不足及发展方向。     

Effects of copper chloride on formation of polychlorinated dibenzofurans in model waste incineration in a laboratory-scale fluidized-bed reactor

Combustion experiments in a laboratory-scale fluidized-bed reactor have been performed to clarify the effects of copper chloride as a catalyst on polychlorinated dibenzofurans (PCDFs) formation in municipal waste incineration. We used model wastes with and without copper chloride (CuCl2 x 2H2O) as a catalyst, both of which contained polyvinyl chloride (PVC) as a chlorine source. Combustion temperature was set to 900 degrees C, and the amount of air supplied was twice as much as the theoretical amount. The experimental setup had been carefully planned to ensure avoidance of the influences of previous experiments. Results of these present experiments revealed that copper chloride in the waste increased the amount of PCDFs formed and made the homologue profile shifted towards the highly chlorinated species. Copper chloride contributes to PCDFs formation by promoting chlorination via catalytic reactions, whereby the reaction could be important in that organic matters are chlorinated directly by chlorinated compounds related to Deacon reaction such as copper chloride. It was elucidated that characteristic isomer distribution patterns appeared in case the waste contained copper chloride. It is probable in our experiment with copper chloride that PCDFs are mainly formed via catalytic reactions of copper compounds and carbon.     

Mechanisms of episodic acidification in low-order streams in Maine, USA

Five factors contribute to episodic depressions in pH and ANC during hydrologic events in low-order streams in Maine: (1) increases of up to 50 microeq litre(-1) NO3; (2) increases of up to 75 microeq litre(-1) organic acidity; (3) increases of as much as 0.3 in the anion fraction of SO4; (4) as much as 100 microeq litre(-1) acidity generated by the salt-effect in soils; and (5) typically < or = 40% dilution by increased discharge. In conjunction with increased discharge, factors 1, 2 or 4 appear necessary to depress pH to less than 5.0. The chemistry of individual precipitation events is irrelevant to the generation of acidic episodes, except those caused by high loading of neutral salts in coastal regions. Increases in discharge, but not necessarily in dilution of solutes, in combination with the chronically high SO4 from atmospheric deposition, provide the antecedent chemical conditions for episodic acidification. Differences in antecedent moisture conditions determine the processes that control output of either ANC or acidifying agents to aquatic systems.     

Structural Dependence of Diurnal Fluctuations of Radon Progeny in Residential Buildings

Movement of radon progeny inside houses is a complex process that depends both on atmospheric conditions and on building structure. The indoor working level (WL) monitored in four houses of differing structures shows regular diurnal fluctuations related to solar warming of the atmosphere. In the two houses with full basements, radon is removed by indoor/outdoor pressure-driven airflow, and basement WL varies inversely with outdoor temperature. In the two houses with half basements open to crawl spaces, radon is drawn into the basement faster than it is removed, so that basement WL varies directly with outside temperature. Average WL's in basements are about twice as high as first floor WL's and as much as 18 times as high as outdoor WL's. Each house shows an individual pattern of radon progeny movement throughout the building.     

Study of chlorothalonil photodegradation in natural waters and in the presence of humic substances

Photodegradation of chlorothalonil was studied in different natural waters (sea, river and lake) as well as in distilled water under natural and simulated solar irradiation. The effect of dissolved organic matter (DOM) such as humic and fulvic substances on the photodegradation rate of chlorothalonil was also studied in simulated sunlight. The presence of DOM enhanced the photodegradation of chlorothalonil with the exception of seawater. The kinetics were determined through gas chromatography electron capture detection (GC/ECD) and the photodegradation proceeds via pseudo-first-order reaction in all cases. Half-life ranged from 1 to 48 h. In natural and humic water chlorothalonil photodegradation gave rise to two different intermediates compared to distilled water demonstrating that the transformation of chlorothalonil depend on the constitution of the irradiated media and especially from DOM. The byproducts identified by GC/MS techniques were: chloro-1,3-dicyanobenzene, dichloro-1,3-dicyanobenzene, trichloro-1,3-dicyanobenzene and benzamide.     

Bilateral environmental cooperation in 1991?V2001 and its role in the improvement of the ecological situation in Estonia

Estonia has made relatively fast progress in developing its environmental policy and drafting legislation during the last decade. Strategic environmental documents and programmes have been elaborated, and Estonia has successfully started to implement the goals set in these documents. Implementation of agreed environmental policy goals requires significant financial resources as well as know-how, and international cooperation is one of the most important sources of them. Bilateral environmental cooperation with Northern and Central European countries, which is based on international regime-like arrangements and is well institutionalised, has been and still is an important source of know-how as well as financial assistance for the improvement of the state of the environment in Estonia. Experience acquired in this cooperation process has also helped Estonia to pave the way towards successful accession negotiations with the European Union.     

浮萍植物在污水处理中的应用研究进展

浮萍科植物是漂浮生长在水流相对平缓的湖泊河湾水面上植物类群，整个植株完全退化为一个呈圆形或椭圆形的叶状体，主要是通过根或叶状体从水中吸收所需的氮磷等各种营养物质。浮萍科植物的氮磷含量和生长速率高并可以耐受多种污水条件，因此这个类群是污水处理生态工程中重要的水生植物类群。以浮萍为主的污水处理系统已得到较多的研究和应用，这类系统最大特点是浮萍的生长可以大量吸收污水中的氮磷，从而具有较高的氮磷去除率，同时生成的生物量可多种方式利用。因此利用这类系统对污水进行氮磷的处理与转化，并将生成的浮萍生物量适当地资源化利用是未来的发展方向。     

浮萍植物在污水处理中的应用研究进展

浮萍科植物是漂浮生长在水流相对平缓的湖泊河湾水面上植物类群,整个植株完全退化为一个呈圆形或椭圆形的叶状体,主要是通过根或叶状体从水中吸收所需的氮磷等各种营养物质.浮萍科植物的氮磷含量和生长速率高并可以耐受多种污水条件,因此这个类群是污水处理生态工程中重要的水生植物类群.以浮萍为主的污水处理系统已得到较多的研究和应用,这类系统最大特点是浮萍的生长可以大量吸收污水中的氮磷,从而具有较高的氮磷去除率,同时生成的生物量可多种方式利用.因此利用这类系统对污水进行氮磷的处理与转化,并将生成的浮萍生物量适当地资源化利用是未来的发展方向.     

Estimation of metal uptake efficiencies from precipitation in mosses in Lithuania

The main sources contributing to heavy metal content in mosses in Lithuania were examined by a comparison of heavy metal concentrations in moss and corresponding deposition levels calculated from bulk deposition analysis. Bulk deposition was collected in open areas as well as under the canopy of trees. Uptake efficiencies in moss were calculated for Cd, Cr, Cu, Fe, Mn, Ni, V and Zn. All elements in moss except Pb and Cd appeared to be more or less influenced by sources other than air pollution. The general order of this influence on the heavy metal content in moss was observed as follows: Ni < V < Cr < Zn < Fe < Mn. The contents of Mn and Zn in moss were greatly influenced by leaching from the canopy while Pb was the only element which showed a net metal retention by the canopy. Concentrations of Fe and Cr in moss were dominating due to contribution from soil dust.     

测量试样中的氮氧化物含量不确定度评定

以实际监测数据为例，详细描述测量试样中的NOx含量不确定度评定方法，包括不确定度源的分析，A类标准不确定度评定、B类标准不确定度评定、合成标准不确定度和扩展不确定度等，对不确定度的分量作了详尽的分析和计算。     

Butyltin residues in livers of humans and wild terrestrial mammals and in plastic products

Butyltin compounds (BTs) including mono-(MBT), di-(DBT) and tributyltin (TBT) were determined in livers of humans and wild terrestrial mammals, such as raccoon dogs (Nyctereutes procyonoids) and monkeys (Macaca fuscata) from Japan. In addition, 22 samples of plastic products were analyzed. BT residues were detected in all the liver samples of humans and raccoon dogs, with concentrations of <360 ng/g wet wt, whereas concentrations in the liver of monkeys were either less than the detection limit or were only in trace levels. Elevated concentrations of BTs, particularly DBT (<140,000 ng/g) and MBT (<130,000 ng/g), were found in some plastic products, such as baking parchments made from siliconized paper and gloves made up from polyurethane. The results of a cooking test using the above baking parchment indicated the transfer of BTs to foodstuffs. These observations suggest expansion of BT contamination among terrestrial mammals. BT pollution from industrial appliances, such as plastic stabilizers and catalysts other than those of marine origin as antifouling agents, are suggested as alternative sources of exposure.     

Contents and sources of DDT impurities in dicofol formulations in Turkey

Background, aim, and scope  Dicofol is widely used as a pesticide in agriculture applications. Since dicofol is mainly synthesized from dichlorodiphenyltrichlorethane (DDT), it contains DDT as an impurity. The European Community has forced Prohibition Directive 79/117/EEC to reduce DDT in dicofol formulations. Specifically, DDT content in a dicofol formulation cannot exceed 0.1%. The goal of this project was to determine the DDT content in dicofol formulations used in Turkey. Materials and methods  Samples of all the dicofol formulations in Turkey were collected to quantify DDT and DDT-related compounds. Four replicates were used for each sample. GC/MS/MS was used to analyze p,p′ and o,p′ isomers of DDT, DDD, and DDE. A HPLC was used to determine p,p′-Cl-DDT concentrations. Results  The total DDT content of the formulated dicofol was found between 0.3% and 14.3%. The concentration of p,p′-DDE ranged from 167 to 1,042 mg kg⁻¹ in dicofol samples. p,p′-DDT concentrations were found to be 32 to 183 mg kg⁻¹. The o,p’-DDT level ranged from 2 to 34 mg kg⁻¹ in the dicofol formulations analyzed. Discussion  It was estimated that 617.8 kg of DDT was released from dicofol. The main impurity was identified as p,p-Cl-DDT. Based on these results, dicofol serves as a continuing source of DDT contamination. Conclusions  All DDT concentrations in dicofol samples analyzed were higher than the permitted 0.1% level of Prohibition Directive 79/117/EEC. The reduction of dicofol is critical since it serves as a continual source of DDT contamination. Recommendations and perspectives  DDT has been found in soil, water, and air samples. Dicofol has been identified as a contributor to continued DDT contamination in soil and water. More studies are needed to ascertain the source of DDT in the air.