基于16S rDNA-DGGE和FDC技术对富营养化湖泊不同生态修复工程区细菌群落结构的研究

于2005年10月在太湖梅梁湾水体生态修复工程区中采集不同生物净化区水样,直接提取水样中的总DNA,以细菌16SrDNA通用引物进行V3区PCR扩增,PCR产物经DGGE(变性凝胶梯度电泳)分离后,获得水体细菌群落的16S rDNA指纹图谱;并运用FDC(表面荧光直接计数)方法对不同生物净化区的细菌丰度进行了测定.结果表明,随着净化处理程度的增加,细菌群落多样性呈现上升趋势,DGGE条带从未实施生态修复的梅梁湾中的13条上升到沉水植物恢复区的25条;细菌数量的变化则呈现显著下降趋势,由工程区外围(重富营养区)的5.36×106cells/mL下降到生态修复区的2.06×106cells/mL.生态修复工程的实施改善了水体的生境条件,提高了水体的自净能力,促进了细菌多样性的恢复.图6表1参40     

链格孢菌菌株致病性及其遗传差异性

对分离自紫茎泽兰的19个链格孢菌菌株的致病性进行了比较研究，并对这19个菌株和其它来源的3个菌株的5．8S rDNA及其两侧的ITS1区和ITS2区进行了序列分析．结果显示，链格孢菌菌株的致病性差异明显；21株链格孢菌菌株在5．8SrDNA及其两侧的转录问区（ITS区）的序列无差异，而与百日草链格孢菌（Alternaria zinnine）的序列差异显著，表明21株链格孢菌菌株属种内变异．采用AFLP分子标记技术对21株链格孢菌的DNA扩增片段长度多态性进行了分析，结果表明，链格孢菌自然变异群体内存在很高的遗传多样性．链格孢菌菌株的相似性与菌株的地理来源有一定的相关性，但基于AFLP标记划分的AFLP类群与基于寄主病情指数划分的致病力类群问关系不相一致；起始菌株与变异菌株相似性显著，但二者和致病性的关系不显著．图2表1参18     

物候学在生态监测中的应用

本文介绍了物候学以及物候观测的主要方法,对物候学与生态监测的关系以及在生态监测中的应用进行了探讨.     

Adsorption and mechanistic study of the invasive plant-derived biochar functionalized with CaAl-LDH for Eu(III) in water

Herein, we developed the invasive plant-derived biochar (IPB) functionalized with CaAl-LDH at five mass ratios using a physical mixture method, assessed their adsorption perform for Eu(III), and explored the relative mechanisms. Results show that the IPB successfully loaded CaAl-LDH in five composites and their Eu(III) sorption affinities were strongly affected by solution pH, contact time, temperature, and the mass ratio of LDH and IPB. All the sorpiton process for Eu(III) occurred on the heterogeneous surface of five composites and the boundary layer diffusion limited the chemical sorption rate. Interestingly, the CaAl-LDH/IPB composite with high ratio of IPB had higher sorption capacity than the one with high ratio of LDH due to larger porosity of the former. Three mechanisms containing ion exchange between Al and Eu ions, surface complexation with carboxyl- and oxygen-containing functional groups, and precipitation were involved in the Eu(III) sorption, but the dominant sorption mechanism for each CaAl-LDH/IPB composite differed with different mass ratio of CaAl-LDH and IPB. In composite with more IPB (e.g., CaAl-LDH/IPB-13), both ion exchange and surface complexes dominated the sorption process and the intensity of Eu³⁺ was identified with the one of Eu₂O_3. Whereas in composites with high LDH, ion exchange dominated the sorption and the intensity of Eu³⁺ was obviously higher than the one of Eu₂O₃. This research will provide a new perspective for the application of the LDH/biochar materials.     

Phosphine production in anaerobic wastewater treatment under tetracycline antibiotic pressure

The influence of tetracycline(TC) antibiotics on phosphine(PH_3) production in the anaerobic wastewater treatment was studied. A lab-scale anaerobic baffled reactor with three compartments was employed to simulate this process. The reactor was operated in a TC-absence wastewater and 250 μg/L TC-presence wastewater for three months after a start-up period,respectively. The responses of p H, oxidation–reduction potential(ORP), chemical oxygen demand(COD), total phosphorus(TP), enzymes activity(dehydrogenase and acid phosphatase),and microbial community were investigated to reveal the effect of TC on PH_3 production.Results suggested that the dehydrogenase(DH) activity, acid phosphatase(ACP) activity and COD have positive relationship with PH_3 production, while p H, ORP level and the TP in liquid phase have negative relationship with PH_3 production. With prolonged TC exposure, decrease in p H and increase in DH activity are beneficial to PH_3 production, while decrease in COD and ACP activity are not the limiting factors for PH_3 production.     

Fast screening compositions of PM2.5 by ATR-FTIR: Comparison with results from IC andOC/EC analyzers

Chemical speciation of fine particles or PM_(2.5) collected on filters is still a costly and timeconsuming task. In this study, filter-based PM_(2.5) samples were collected during November–December 2013 at four sites in Guangzhou, and the major components were fast screened(~7 min per filter sample) by Attenuated Total Reflectance(ATR)-Fourier Transform Infrared Spectroscopic(FTIR) in comparison with that measured by Organic carbon/Element carbon(OC/EC) analyzer and Ion Chromatography(IC). The concentrations of nitrate, ammonium, sulfate,primary organic carbon(POC) and secondary organic carbon(SOC) measured by OC/EC and IC analyzers were better correlated with their infrared absorption peak heights at 1320 cm~(-1) for nitrate, 1435, 3045 and 3215 cm~(-1) for ammonium, 615 cm~(-1) for sulfate, 690, 760 and 890 cm~(-1) for POC and 1640 and 1660 cm~(-1) for SOC respectively, during polluted days(PM_(2.5) 75 μg/m~3) than during clean days(PM_(2.5)≤ 75 μg/m~3). With the evolution of a haze episode during our field campaign, the concentrations of the major PM_(2.5) components displayed consistent variations with their infrared absorption peak heights, suggesting ATR-FTIR could be a fast and useful technique to characterize filter-based PM_(2.5) compositions particularly during pollution events although cautions should be taken when PM_(2.5) levels are low. Notably, elevated PM_(2.5) mass concentrations occurred with enhanced ratios of [NO_(-3)]/[SO_4~(2-)] and [NH~(+4)]/[SO_4~(2-)], implying that nitrogenous components play vital roles in the PM_(2.5) pollution events in the study region.     

Influences of accumulated mileage and technological changes on emissions of regulated pollutants from gasoline passenger vehicles

In this study, the influences of accumulated mileage(deterioration) and technological changes(emission standards) on emission factors(EFs) of regulated pollutants(CO, HC, and NO_x) from gasoline passenger vehicles were investigated based on Inspection and Maintenance(I/M) data using the chassis dynamometer method. The accumulated mileage of passenger vehicles was significantly linearly correlated with vehicle age. For most cases,the average EFs of CO, HC and NO_x were significantly linearly correlated with accumulated mileage, indicating that emission deterioration had a significant impact on pollutant EFs.Implemented emission standards markedly influenced the EFs of regulated pollutants, and EFs markedly decreased with progressing emission standards. The present study also compared EFs of regulated pollutants between this study and the International vehicle emission(IVE) model, and marked differences in EFs were seen with variations in emission standards, vehicle types and accumulated mileage; NO_x EFs in this study were higher than in the IVE model. The results provide new insight into estimating regulated pollutant emissions using the IVE model.     

苎麻麻骨水溶物的溶出影响因素及其组成

为探讨生物质材料吸附重金属过程中溶出物的溶出规律及成分,以苎麻麻骨为材料,在实验室模拟其吸附Cd2+废水条件下,考察溶出时间、温度、pH、苎麻麻骨粒径及ρ(Cd2+)对苎麻麻骨水溶物DOC溶出量的影响,通过气相色谱-质谱法对溶出物成分进行鉴定,并利用扫描电子显微镜(SEM)、红外光谱(FTIR)、热重分析(TGA)等技术对溶出物溶出前后苎麻麻骨表面物化性质进行了表征. 结果表明:在弱酸性(pH为5)条件下,苎麻麻骨DOC溶出量高于65.90 mg/L. 各因素对DOC溶出量的影响程度不同,以粒径及温度的影响最大,随着粒径由1 mm增至20 mm,DOC溶出量由78.37 mg/L迅速降至60.14 mg/L,降低了18.23 mg/L;升温可促进苎麻麻骨DOC溶出量的增加,随着温度由5 ℃升至55 ℃,DOC溶出量增加了13.63 mg/L. 提取液pH、溶出时间、ρ(Cd2+)对DOC溶出量的增加量分别为5.08、4.60、3.11 mg/L. 溶出物溶出前后苎麻麻骨表面无显著变化,但溶出后的苎麻麻骨表面易溶于水的官能团数量显著减少. 溶出物中鉴定出9类物质(共19种化合物),以酮类和酯类居多,表明苎麻麻骨表面不带电.