土著致病菌及其胞外物在生物防治斑马贝中的作用

无脊椎动物斑马贝(Dreissena polymorpha) 的生物污损造成了巨大的经济损失,而应用从斑马贝体内分离出的土著菌株及其体外代谢产物对它进行生物防治是一种经济效益显著且对环境友好的方法.本文主要报导从斑马贝体内分离的土著菌株中筛选出致病菌并研究该细菌及其代谢产物对它的控制作用.在三十多种土著菌株中,中间气单胞菌( Aeromonas media),维罗纳气单胞菌(A. veronii),杀鲑气单胞菌杀鲑亚种(A. salmonicida subsp. salmonicida)和腐败希瓦氏菌(Shewanella putrefaciens)是幼体斑马贝的致命致病菌.当接种量为每只斑马贝107 个细菌时,接种中间气单胞菌、杀鲑气单胞菌杀鲑亚种和腐败希瓦氏菌的5 d 死亡率为100%,而维罗纳气单胞菌为65%.通过扫描电镜(SEM)发现,垂死的斑马贝肌肉组织被破坏并含有大量的细菌.4种细菌代谢产物的不同组分表现出对斑马贝不同的致死效果,在所研究的3种不同Mr组分中(Mr<5×103,5×103～10×103及>10×103),>10 ×103组分具有最高致死率.这些结果为控制贝类无脊椎动物的生物污损提供了新方法. 图4 参24     

钒胁迫对水稻幼苗生理生化和富集特性的影响

水稻（Oryza.sativa L.）是我国最重要的粮食作物之一,水稻产量占粮食总产量的一半以上,一旦水稻受到重金属污染,将会影响水稻植株的正常生长和生理特性。目前关于钒胁迫对水稻植株生理特性指标的影响方面报道较少。通过水培实验,研究了不同钒（V）质量浓度（0、4、8、12、16、20 mg·L-1）对水稻幼苗（Oryza.sativa L）生理生化和富集特性的影响。结果表明：随着V胁迫浓度的增加,叶绿素含量、可溶性蛋白含量、过氧化氢酶（CAT）活性、过氧化物酶（POD）活性、超氧化物歧化酶（SOD）等均呈现先上升、后下降的变化趋势。当ρ（V）≤12 mg·L-1,与对照相比较,叶绿素含量、可溶性蛋白含量和酶活性增大了135.3%、104.2%、77.8%（CAT）、84.5%（POD）和273.2%（SOD）;当ρ（V）〉12 mg·L-1,则分别降低37.2%、39.4%、41.1%、24.1%和24.5%。随着 V 胁迫浓度的增加,丙二醛（MDA）含量和细胞膜透性逐渐增大,与对照相比,分别增加了38.5%~289.3%、21.2%~303.2%,根系活力下降了10.9%~82.2%。可见,低ρ（V）（≤12 mg·L-1）对水稻幼苗的生长有一定的刺激作用,水稻幼苗自身保护酶表现出较强的自我调节能力;高ρ（V）（〉12 mg·L-1）明显抑制叶绿素和蛋白合成、抗氧化酶活性和根系活力,伤害了细胞质膜系统,影响水稻幼苗的生长发育。不同V浓度胁迫下,水稻幼苗累积的V含量为：根〉茎叶。随着V胁迫浓度增加,水稻幼苗各器官V含量增大,其中根部增幅远大于茎叶,当ρ（V）从5 mg·L-1增加到40 mg·L-1,与对照相比较,根部增加了0.98~25.3倍,茎叶部增加了0.26~4.74倍。生物富集系数（BF）先增加后降低,最大值为2.8408;迁移系数（TF）下降,最低值为0.1170,说明水稻对V有较强的富集能力,但迁移能力较低,积累的V主要富集在根部,可减轻V对地上部植物的危害。     

Cu2+或表面活性剂AE对黄鳝肝损伤的超微结构观察

利用透射电镜研究了亚致死浓度的Cu^2 或表面活性剂AE(脂肪醇聚氧乙烯醚)对黄鳝肝细胞结构的损伤作用．观察发现，在ρ(Cu^2 )=4．5mg／L的污染环境中，黄鳝肝脏细胞核变形，染色质凝集，内质网囊泡化，细胞质中出现较多的溶酶体和过氧化物酶体；在ρ(AE)=4．0mg／L的表面活性剂污染下，黄鳝肝脏细胞核变形，内质网呈线状，溶酶体、过氧化物酶体体积大、数量多，部分细胞质解体，细胞中出现空腔甚至死亡．图版1参10     

Coupling a land use model and an ecosystem model for a crop-pasture zone

This paper describes the development of a land use model coupling ecosystem processes. For a given land use pattern in a region, a built-in regional ecosystem model (TESim) simulates leaf physiology of plants, carbon and nitrogen dynamics, and hydrological processes including runoff generation and run-on re-absorption, as well as runoff-induced soil erosion and carbon and nitrogen loss from ecosystems. The simulation results for a certain period from 1976 to 1999 were then used to support land use decisions and to assess the impacts of land use changes on environment. In the coupling model, the land use type for a land unit was determined by optimization of a weighted suitability derived from expert knowledge about the ecosystem state and site conditions. The model was applied to the temperate crop-pasture band in northern China (CCPB) to analyze the interactions between land use and major ecosystem processes and functions and to indicate the added value of the feedbacks by comparing simulations with and without the coupling and feedbacks between land use module and ecosystem processes. The results indicated that the current land use in CCPB is neither economical nor ecologically judicious. The scenario with feedbacks increased NPP by 46.78 g C m⁻² a⁻¹, or 32.23% of the scenario without feedbacks, also decreased soil erosion by 0.65 kg m⁻² a⁻¹, or 23.13%. Without altering the regional land use structure (proportions of each land use type). The system developed in this study potentially benefits both land managers and researchers.     

专家系统在废水生物处理操作和控制中的应用

本文介绍了国外近二十年来专家系统在废水生物处理工艺控制领域的应用及开发的典型系统,分析了废水生物处理工艺难于控制的原因、各类系统的结构和特点及目前废水处理专家系统的不足,探讨了废水生物处理专家系统今后应深入研究的问题及方向     

铬渣的热解无害化处理

采用热解工艺无害化处理铬渣,探讨了稻秆在铬渣无害化处理中的作用.研究了热解温度、稻秆与铬渣质量比、铬渣粒径及保温时间对铬渣热解无害化处理的影响,并分析了热解前后热解产物中铬元素形态的变化.结果表明,热解工艺能有效地将铬渣中Cr(Ⅵ)还原,稻秆热解过程中产生的气相挥发分对Cr(Ⅵ)的还原起核心作用.较为适宜的热解条件:热解温度为400 ℃,稻秆与铬渣质量比为0.10,铬渣粒径<2 000 μm,保温时间为10 min.在该热解条件处理下,热解产物中的Cr(Ⅵ)质量浓度为121 mg/kg,低于热解前铬渣中的Cr(Ⅵ)(3 400 mg/kg).热解后,可交换态及碳酸盐结合态铬含量降低,大部分铬转化成了稳定的有机结合态和残渣态,极大地降低了铬渣的危害.第一作者:张大磊,男,1982生,博士研究生,研究方向为固体废弃物热处理.     

Role of water chemistry on estrone removal by nanofiltration with the presence of hydrophobic acids

Hydrophobic acid organic matter (HpoA) extracted from treated effluent has been known to improve the rejection of steroid hormone estrone by reverse osmosis (RO) and nanofiltration (NF) membranes. In this study, the effects of solution chemistry (solution pH and ionic strength) on the estrone rejection by NF membrane with the presence of HpoA were systematically investigated. Crossflow nanofiltration experiments show that the presence of HpoA significantly improved estrone rejection at all pH and ionic strength levels investigated. It is consistently shown that the “enhancement effect” of HpoA on estrone rejection at neutral and alkaline pH is attributed to the binding of estrone by HpoA macromolecules via hydrogen bonding between phenolic functional groups in feed solutions, which leads to an increase in molecular weight and appearance of negative charge. The membrane exhibited the best performance in terms of estrone rejection at pH 10.4 (compared to pH 4 and pH 7) as a result of strengthening the electrostatic repulsion between estrone and membrane with the presence of HpoA. At neutral pH level, the ability of HpoA macromolecules to promote estrone rejection became stronger with increasing ionic strength due to their more extended conformation, which created more chances for the association between estrone and HpoA. The important conclusion of this study is that increasing solution pH and salinity can greatly intensify the “enhancement effect” of HpoA. These results can be important for NF application in direct/indirect potable water reuse.     

响应曲面法优化絮凝处理木薯淀粉废水

采用中心复合实验设计和响应面分析法研究复合絮凝剂聚合氯化铝锌(PAZC)和聚合氯化铝(PAC)混凝处理木薯淀粉废水,进行设计和分析,以溶液pH值和絮凝剂用量为考察因素,分别以COD、浊度去除率为考察指标,选用最佳优化数学模型描述考察指标和考察因素之间的数学关系,并以设定PAZC和PAC对COD去除率(65%),浊度去除率(90%)和SS去除率(90%)的目标值,通过等高线叠加图预测最优实验条件,得到PAZC投量为6.5 mg/L,pH为7.7时,COD去除率和浊度去除率分别达到最大为76.6%和99.9%;PAC投量为19.2 mg/L,pH为7.8时,COD去除率和浊度去除率最大值分别为64.4%和97.1%。经对最优条件进行验证,预测值与验证实验平均值接近。     

An overview of the methods used in the characterisation of natural organic matter (NOM) in relation to drinking water treatment

Natural organic matter (NOM) is found in all surface, ground and soil waters. During recent decades, reports worldwide show a continuing increase in the color and NOM of the surface water, which has an adverse affect on drinking water purification. For several practical and hygienic reasons, the presence of NOM is undesirable in drinking water. Various technologies have been proposed for NOM removal with varying degrees of success. The properties and amount of NOM, however, can significantly affect the process efficiency. In order to improve and optimise these processes, the characterisation and quantification of NOM at different purification and treatment processes stages is important. It is also important to be able to understand and predict the reactivity of NOM or its fractions in different steps of the treatment. Methods used in the characterisation of NOM include resin adsorption, size exclusion chromatography (SEC), nuclear magnetic resonance (NMR) spectroscopy, and fluorescence spectroscopy. The amount of NOM in water has been predicted with parameters including UV-Vis, total organic carbon (TOC), and specific UV-absorbance (SUVA). Recently, methods by which NOM structures can be more precisely determined have been developed; pyrolysis gas chromatography-mass spectrometry (Py-GC-MS), multidimensional NMR techniques, and Fourier transform ion cyclotron resonance mass spectrometry (FTICR-MS). The present review focuses on the methods used for characterisation and quantification of NOM in relation to drinking water treatment.     

Removal of Alachlor from Water by Catalyzed Ozonation in the Presence of Fe2+, Mn2+, and Humic Substances

Abstract

The effects of Fe(II), Mn(II) and humic substances on the catalyzed ozonation of alachlor, an endocrine disruptor were investigated. Results revealed that small amounts of Fe(II), Mn(II), and humic substances could enhance the ozonation of alachlor, but larger amounts of them would retard the oxidation. These results were successfully identified by an electron paramagnetic resonance (EPR) spectroscopy/spin-trapping method that could quantify hydroxyl radicals. The production of hydroxyl radicals was obviously increased with the increasing of Fe(II) concentration, which contributed to enhance ozonation at low concentrations. But the excess Fe(II) consumed some of the radicals when it was added at a higher concentration (1.5 mg/L). However, no obvious radicals were observed when a different amount of Mn(II) was used, and the catalytic ozonation of alachlor by Mn(II) mainly followed the mechanism of “active sites created on the surface of MnO₂.” The radical pathway was followed when alachlor was ozonated with different concentrations of humic substances because of its radical initiating, promoting, and inhibiting effects.