重金属Cd、Cu对小麦(Triticum aestivum)幼苗生理生化过程的影响及其毒性机理研究

对Cd、Cu单因子处理下小麦幼苗叶片和根系的SOD、POD酶活、可溶性蛋白含量以及叶片中叶绿素含量的变化进行了研究.结果表明,Cd、Cu胁迫下,小麦幼苗受到损伤的明显症状之一是叶片叶绿素含量下降;小麦植株叶片POD、SOD酶活能够被诱导而升高;重金属Cd、Cu对小麦幼苗根系的损伤较叶片大;重金属对小麦幼苗的毒害机理之一是抑制了蛋白质的生物合成;重金属引起的各个生化指标随着处理浓度和处理时间的变化远比有机污染物(如豆磺隆)简单.     

反硝化生物膜对PBS表面形态及化学组分的影响

PBS是一种新型的可生物降解聚合物(BDPs),可以用做反硝化碳源和生物膜载体,去除饮用水源水中的硝酸盐.利用红外光谱和扫描电子显微镜对反硝化生物膜生长前后PBS颗粒表面形态、化学组成的变化进行了分析.结果表明,PBS仅在微生物作用下降解并为反硝化菌提供碳源.PBS颗粒可以在12 h内使进水中53 mg·L^-1的硝态氮降低到10 mg·L^-1以下(我国饮用水水质标准为:NO₃^--N<15 mg·L^-1).红外光谱表明,反硝化微生物附着生长后其PBS在2 925 cm^-1和2 850 cm^-1附近的吸收带以及3 200 cm^-1～3 410 cm^-1处峰值减弱,说明PBS材料中甲基、羟基官能团比例下降,而其它官能团没有发生明显的变化,PBS的主要单体组分淀粉和乙烯都可以被反硝化微生物用作碳源.扫描电子显微镜观察结果表明,反硝化生物膜附着生长后,PBS颗粒表面会出现空洞,扩大了生物膜生物附着生长的表面积,有利于形成致密的反硝化生物膜,对反硝化菌形成保护作用.     

Perfluorinated Surfactants in Surface and Drinking Waters (9 pp)

Background, Aim and Scope In this paper recent results are provided of an investigation on the discovery of 12 perfluorinated surfactants (PS) in different surface and drinking waters (Skutlarek et al. 2006 a, Skutlarek et al. 2006 b). In the last years, many studies have reported ubiquitous distribution of this group of perfluorinated chemicals, especially perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) in the environment, particularly in wildlife animal and human samples (Giesy and Kannan 2001, Houde et al. 2006, Prevedouros et al. 2006). Perfluorinated surfactants (e.g. PFOS and PFOA) have shown different potentials for reproductory interference and carcinogenity in animal experiments as well as partly long half-lives in humans (Guruge et al. 2006, FSA UK 2006a, FSA UK 2006b, 3M 2005, OECD 2002, Yao and Zhong 2005). They possess compound-dependent extreme recalcitrance against microbiological and chemical degradation and, in addition, they show variable potentials for bioaccumulation in animals and humans (Houde et al. 2006). Materials and Methods: Surface and drinking water samples were collected from different sampling sites: - Surface waters: samples taken from the rivers Rhine, Ruhr, Moehne and some of their tributaries. Further samples were taken from the Rhine-Herne-Canal and the Wesel-Datteln-Canal. - Drinking waters: samples taken in public buildings of the Rhine-Ruhr area. After sample clean-up and concentration by solid-phase extraction, the perfluorinated surfactants were determined using HPLC-MS/MS. Results: All measured concentrations (sum of seven mainly detected components) in the Rhine river and its main tributaries (mouths) were determined below 100 ng/L. The Ruhr river (tributary of the Rhine) showed the highest concentration (94 ng/L), but with a completely different pattern of components (PFOA as major component), as compared with the other tributaries and the Rhine river. Further investigations along the Ruhr river showed remarkably high concentrations of PS in the upper reaches of the Ruhr river and the Moehne river (tributary of the Ruhr) (Ruhr: up to 446 ng/L, Moehne: up to 4385 ng/L). The maximum concentration of all drinking water samples taken in the Rhine-Ruhr area was determined at 598 ng/L with the major component PFOA (519 ng/L). Discussion: The surface water contaminations most likely stem from contaminated inorganic and organic waste materials (so-called 'Abfallgemisch'). This waste material was legally applied to several agricultural areas on the upper reaches of the Moehne. Perfluorinated surfactants could be detected in some suchlike soil samples. They contaminated the river and the reservoir belonging to it, likely by superficial run-off over several months or probably years. Downstream, dilution effects are held responsible for decreasing concentrations of PS in surface waters of the Moehne and the Ruhr river. In analogy to the surface water samples, PS (major component PFOA) can be determined in many drinking water samples of the Rhine-Ruhr area where the water supplies are mainly based on bank filtration and artificial recharge. Conclusions: The concentrations found in drinking waters decreased with the concentrations of the corresponding raw water samples along the flow direction of the Ruhr river (from east to west) and were not significantly different from surface water concentrations. This indicates that perfluorinated surfactants are at present not successfully removed by water treatment steps. Recommendations and Perspectives: Because of their different problematic properties (persistence, mobility, toxicity, bioaccumulation), the concentrations of specific perfluorinated surfactants and their precursors in drinking waters and food have to be minimised. Therefore, it is of utmost importance to take the initiative to establish suitable legal regulations (limitations/ban) concerning the production and use of these surfactants and their precursors. Furthermore, it is indispensable to protect water resources from these compounds. A discussion on appropriate limit values in drinking water and foodstuffs is urgently needed. Concerning the assumed soil contamination, the corresponding regulation (Bioabfall-Verordnung 1998 – Regulation on Organic Waste 1998) should be extended to allow the control of relevant organic pollutants.     

EFFECTS OF ADVANCED WASTEWATER TREATMENT ON THE QUALITY OF WHITE RIVER,INDIANA1

ABSTRACT: In 1983, the City of Indianapolis, Indiana, completed construction of advanced wastewater treatment (AWT) systems to enlarge and upgrade its existing Belmont Road and South port Road secondary treatment plants. A nonparametric statistical procedure, a modified form of the Wilcoxon-Mann-Whitney rank-sum test, was used to test for trends in water quality at two upstream and two downstream sites on White River and at the two treatment plants. Results comparing the pre- (1978–1980) and post- (1983–1986) AWT periods show statistically significant improvements in the quality of the treated effluent and of the White River downstream from the plants. Water quality at sites upstream from the city was relatively constant during the period of study. Total ammonia (as N) decreased 14.6 mg/L and BOD₅ (five-day biochemical oxygen demand) decreased 10 to 19 mg/L in the two effluents. Total ammonia in the river downstream from the plants decreased 0.8 to 1.9 mg/L and BOD₅ decreased 2.3 to 2.5 mg/L. Nitrate (as N) increased 14.5 mg/L in the plant effluents and 2.0 to 2.4 mg/L in the river because of in-plant nitrification. Dissolved oxygen concentration in the river increased about 3 mg/L because of reduced oxygen demand for nitrification and biochemical oxidation processes.     

某城市建筑泥浆污染现状调查研究

以某城市为例,研究城市建筑泥浆的污染现状,并分析泥浆受到污染的原因.结果表明:对照《地表水环境质量标准》(GB 3838-2002)中的Ⅳ类标准限值,调研的4个工地泥浆水全部超标;该城市地层土壤中的有机质、总氮、总磷含量高是泥浆水超标的重要原因,工地制浆使用的地表水和污水也不能满足Ⅳ类水质的要求.在建筑工地的管理中,应...     

城市土壤污染研究现状与趋势

城市土壤是城市生态环境系统的有机组成部分,对城市的可持续发展有着重要的意义.城市化和工业化进程的加快,造成城市土壤污染、侵蚀、酸化和硬化以及土壤生物和植被退化等一系列较为严重的城市环境问题,直接危及到城市居民的健康和安全;因此,城市土壤污染问题已经引起人们的高度重视.近10多年来,国内外有关城市土壤重金属污染,微有机物污染,生源要素污染和城市土壤污染的环境与健康风险评价等诸多研究取得了一系列的研究成果.本文主要就以上研究成果进行了较为系统地总结与阐述,并且在此基础上提出了今后有关城市土壤污染研究的发展重点与趋势,以期为改善城市生态环境质量提供重要的科学依据.     

转cry1Ab基因水稻中毒蛋白的表达、分泌及其在土壤中的残留

研究了转cry1Ab基因水稻(克螟稻)中Cry1Ab毒蛋白的表达、根系分泌及其在土壤中的残留规律.结果表明,分蘖始期至成熟期,克螟稻地上部和根部中的Cry1Ab毒蛋白的表达量(FW)分别为3.23～8.22 μg/g和0.68～0.89 μg/g.生育期间克螟稻根系分泌的Cry1Ab毒蛋白含量仅为1.66～48.02 ng/(株·d).试验证实,克螟稻根际土中的Cry1Ab毒蛋白残留含量低于检测限(<0.5ng/g 干燥土).生物测定还表明,克螟稻根际土及其提取液对棉铃虫初孵幼虫和3龄幼虫不产生致死性效应.相对于Cry1Ab毒蛋白的根系分泌转移,克螟稻秸秆还田对土壤环境的影响应引起重视.     

某冶炼厂周边土壤环境Cd元素现状调查、污染预警及综合治理

对某冶炼厂以南约30km^3的区域进行了Cd元素土壤地球化学调查,分析了造成Cd富集的原因。通过统计分析,总结了土壤中Cd含量的空间分布特征(包括区域分布和垂向分布),并结合Cd元素的赋存形式、迁移机制对这些特征的成因进行了较为具体的解释。计算了该区cd的污染指数,以及受不同程度污染的土壤面积占研究区面积的百分比。运用“化学定时炸弹”的理论,对该区土壤达到I}缶界含量的年限进行了估测。针对该区的污染来源及状况,提出了综合治理对策。     

爆炸波在饱和土介质中传播时压力变化规律的试验研究

介绍了在Φ900平面波加载器中进行的饱和土爆炸波传播试验,通过试验比较系统地研究了爆炸波在饱和土自由场中的传播规律及其在刚性边界上的反射问题。试验表明饱和土中的气体含量是控制波传播规律的主要因素,在深度方向上自由场应力峰值可能随深度增加,而在刚性边界上荷载反射系数可能>2。对饱和土与非饱和土中波传播规律的区别,在确定饱和土中结构的设计荷载时必须给予极大的关注。     

碳源对微生物硝酸盐异化还原成铵过程的影响

微生物通过异化性硝酸盐还原成铵(DNRA)途径,硝态氮转化为仍可生物再利用的铵盐。以琥珀酸钠、柠檬酸钠、酒石酸钾钠为碳源,研究碳源的差异对有氧条件下微生物通过DNRA途径产铵的影响。结果显示,以琥珀酸钠和柠檬酸钠为碳源,初始浓度为20 mmol/L是较佳的实验条件,此时C/N约为1.5～2.0,NH4+-N质量浓度30.0～45.0 mg/L,最高产铵率分别为29.9%和27.0%;以酒石酸钾钠为碳源则在初始浓度为30 mmol/L,C/N约为2.0,NH4+-N质量浓度为40.0～45.0 mg/L时,最高产铵率为30.7%。反硝化和DNRA过程是同时存在的,培养液中NO3--N浓度的下降伴随着中间产物NO2--N的积累和NH4+-N浓度的升高。