孑遗植物四合木(Tetraenamongolica)迁地保护中的光合作用日变化特征与生理生态适应性

为了进一步廓清迁地保护条件下孑遗植物四合木（Tetraena mongolica）的光合生理生态适应性,在分析了瞬时光合效率的基础上,应用LI-6400光合作用测定系统测定了迁地保护试验区的四合木以及原生境伴生种白刺（Nitraria tangutorum）的光合作用日变化,并测定了其生长量。结果表明：四合木实生苗的生长南北冠幅大小依次为乌海四合木核心区实生苗（26.48 cm×27.26 cm）>鄂尔多斯实生苗（21.27 cm×21.75 cm）>阿拉善实生苗（19.25 cm×18.27 cm）。在原生境地乌海四合木核心区种植的实生苗与阿拉善实生苗之间的生长量存在显著差异（P≤0.01）,与鄂尔多斯实生苗之间的生长量存在显著差异（P≤0.05）。迁地保护条件下四合木生实生苗植株叶片光合速率Pn日变化均呈“双峰”曲线。不同试验区四合木光合作用日变化（Pn）、蒸腾速率（Tr）、气孔导度（Gs）和胞间 CO2浓度（Ci）均表现出明显的分异。迁地保护四合木条件下原生境地栽培的四合木实生苗的光合速率>鄂尔多斯栽培的四合木实生苗的光合速率>阿拉善栽培的四合木实生苗。鉴此可以作进一步推论,孑遗濒危植物四合木从原生境地西鄂尔多斯核心区（乌海）东移进行迁地保护具有更高的生理生态适应性和生境适宜性。但完成“从种子到种子”进而实现“保存性和代表性”,最终实现四合木迁地保护的“保持性和防止性”,保持其遗传多样性和遗传稳定性,最终成功实现四合木的迁地保护仍有待作进一步探索和深入研究。     

表观遗传学机制与空气污染的健康效应

空气污染是一个全球性的问题,并且具有深远的环境影响。暴露于空气污染会对人体健康产生许多不同的影响,理解空气污染的健康效应又是一个复杂命题,既要考虑不同类型的污染物同时也要考虑相关疾病的复杂性。然而越来越多的研究表明,表观遗传学在空气污染相关疾病的发生、发展中发挥着重要的作用。空气污染物可引起DNA甲基化、组蛋白修饰和miRNA表达等表观遗传学改变,这种改变往往发生在疾病产生的早期,因此相关研究不仅可以了解疾病的发病机制,而且还为疾病早期诊断和预防筛选可能的标志物。本文综述了表观遗传学的几种修饰方式和空气污染物造成不良健康损伤机制的一些研究进展。     

一株产电菌嗜根考克氏菌(Kocuria rhizophila)的分离及其产电性能优化

本研究以天津泰达污水处理厂污泥浓缩间的污泥为接种物,启动并运行了微生物燃料电池(MFCs).从富集的阳极生物膜上分离得到了一株纯培养的微生物菌种,命名为P2-A-5.研究发现,菌株P2-A-5的16S rDNA序列与菌株Kocuria rhizophila DC2201具有100%的同源性,结合该菌的形态特征和生理生化实验,将其归属为嗜根考克氏菌(Kocuria rhizophila).通过化学剂处理、底物种类和浓度的优化,进一步提高其在微生物燃料电池中的产电性能.结果表明,菌株K.rhizophila P2-A-5经0.5 mg·L-1溶菌酶处理45 min后,接种到以2.0 g·L-1海藻糖为底物的阳极液中运行MFCs,其功率密度达到314.8 m W·m-2,比优化前(74.9 m W·m-2)提高了320.3%.这是首次对K.rhizophila种内微生物产电性能及其在微生物燃料电池中应用的报道,其成果对于丰富产电微生物的多样性,挖掘更多具有高电化学活性的微生物菌种,提高其产电性能具有重要的理论意义.     

Investigation of carbonyl compound sources at a rural site in the Yangtze River Delta region of China

Carbonyl compounds are important intermediates in atmospheric photochemistry, but their primary sources are still not understood well. In this work, carbonyls, hydrocarbons, and alkyl nitrates were continuously measured during November 2011 at a rural site in the Yangtze River Delta region of China. Mixing ratios of carbonyls and hydrocarbons showed large fluctuations during the entire measurement. The average level for total measured volatile organic compounds during the pollution episode from 25th to 27th November, 2011 was 91.6 ppb, about 7 times the value for the clean period of 7th-8th, November, 2011. To preliminarily identify toluene sources at this site, the emission ratio of toluene to benzene (T/B) during the pollution episode was determined based on photochemical ages derived from the relationship of alkyl nitrates to their parent alkanes. The calculated T/B was 5.8 ppb/ppb, significantly higher than the values of 0.2-1.7 ppb/ppb for vehicular exhaust and other combustion sources, indicating the dominant influence of industrial emissions on ambient toluene. The contributions of industrial sources to ambient carbonyls were then calculated using a multiple linear regression fit model that used toluene and alkyl nitrates as respective tracers for industrial emission and secondary production. During the pollution episode, 18.5%, 69.0%, and 52.9% of measured formaldehyde, acetaldehyde, and acetone were considered to be attributable to industrial emissions. The emission ratios relative to toluene for formaldehyde, acetaldehyde, and acetone were determined to be 0.10, 0.20 and 0.40 ppb/ppb, respectively. More research on industrial carbonyl emission characteristics is needed to understand carbonyl sources better.     

Applying a new method for direct collection, volume quantification and determination of N2 emission from water

The emission of N₂ is important to remove excess N from lakes, ponds, and wetlands. To investigate the gas emission from water, Gao et al. (2013) developed a new method using a bubble trap device to collect gas samples from waters. However, the determination accuracy of sampling volume and gas component concentration was still debatable. In this study, the method was optimized for in situ sampling, accurate volume measurement and direct injection to a gas chromatograph for the analysis of N₂ and other gases. By the optimized new method, the recovery rate for N₂ was 100.28% on average; the mean coefficient of determination (R²) was 0.9997; the limit of detection was 0.02%. We further assessed the effects of the new method, bottle full of water, vs. vacuum bag and vacuum vial methods, on variations of N₂ concentration as influenced by sample storage times of 1, 2, 3, 5, and 7 days at constant temperature of 15°C, using indices of averaged relative peak area (%) in comparison with the averaged relative peak area of each method at 0 day. The indices of the bottle full of water method were the lowest (99.5%-108.5%) compared to the indices of vacuum bag and vacuum vial methods (119%-217%). Meanwhile, the gas chromatograph determination of other gas components (O₂, CH₄, and N₂O) was also accurate. The new method was an alternative way to investigate N₂ released from various kinds of aquatic ecosystems.     

Rapid and simple spectrophotometric determination of persulfate in water by microwave assisted decolorization of Methylene Blue

A rapid and simple method for determination of persulfate in aqueous solution was developed. The method is based on the rapid reaction of persulfate with Methylene Blue(MB) via domestic microwave activation, which can promote the activation of persulfate and decolorize MB quickly. The depletion of MB at 644 nm(the maximum absorption wavelength of MB) is in proportion to the increasing concentration of persulfate in aqueous solution. Linear calibration curve was obtained in the range 0–1.5 mmol/L, with a limit of detection of 0.0028 mmol/L. The reaction time is rapid(within 60 sec), which is much shorter than that used for conventional methods. Compared with existing analytical methods, it need not any additives, especially colorful Fe2+, and need not any pretreatment for samples, such as p H adjustment.     

Mercury adsorption characteristics of HBr-modified fly ash in an entrained-flow reactor

In this study, the mercury adsorption characteristics of HBr-modified fly ash in an entrained-flow reactor were investigated through thermal decomposition methods. The results show that the mercury adsorption performance of the HBr-modified fly ash was enhanced significantly. The mercury species adsorbed by unmodified fly ash were HgCl₂, HgS and HgO. The mercury adsorbed by HBr-modified fly ash, in the entrained-flow reactor, existed in two forms, HgBr₂ and HgO, and the HBr was the dominant factor promoting oxidation of elemental mercury in the entrained-flow reactor. In the current study, the concentration of HgBr₂ and HgO in ash from the fine ash vessel was 4.6 times greater than for ash from the coarse ash vessel. The fine ash had better mercury adsorption performance than coarse ash, which is most likely due to the higher specific surface area and longer residence time.     

低浓度苯系物在新疆干旱区土壤中的吸附行为研究

采集新疆干旱区石化废水库附近区域土壤,以苯、甲苯、乙苯、二甲苯(间、对二甲苯)等典型苯系物为研究对象,系统研究低浓度苯系物在干旱区土壤上的吸附行为,分析土壤有机质含量,溶液p H、溶液含盐量、温度对苯系物吸附的影响。结果显示土壤对低浓度苯系物的吸附16 h达到平衡;吸附等温线经拟合后符合Henry直线型吸附模型;土壤对苯系物的吸附量随着土壤有机质含量的增加而增加,土壤有机质含量与吸附量呈显著正相关(P0.01,R2≥0.919);溶液p H值对吸附过程无明显作用;随着溶液含盐量增大,土壤对苯系物的吸附量表现为先减小,再稳定;温度升高会抑制土壤对苯系物的吸附作用。     

四川三岔湖重金属污染与人类活动的关系

沉积物对湖泊重金属污染具有指示作用,通过分析沉积物的污染特征可以揭示湖泊重金属污染的污染历史和污染源。利用210Pb和137Cs定年和沉积物粒度分析,研究了三岔湖沉积物重金属的不同湖区和不同年代的分布特征及形成原因。人类活动强烈影响了重金属的沉积与富集:Cu、Zn与网箱养殖密切相关,Pb则主要源于邻近岸区的交通运输活动,Cr主要来自农业面源污染。受自身化学特性的影响,重金属的含量与沉积物的粒度分布密切相关,也正因此会出现洪水等的特殊年份重金属污染特征的异变。     

闸控河段水质浓度影响关键因子识别

由于闸门调度对河道内的水环境要素具有强烈的扰动作用,故闸控河段的水质变化过程较常规河道更为复杂。为了探析引起闸控河段水质浓度变化的主要制约因素,以槐店闸为研究对象,结合笔者进行的2次实验和其他时期的监测数据,通过偏相关分析和主成分分析的方法识别影响闸控河段水质浓度变化的关键因子,并利用多元线性回归方法分析得到闸控河段水质浓度变化与其关键因子的多元线性回归方程。经过分析初步得到,与高锰酸盐指数浓度变化率有关的关键因子为闸门开度、开启个数、高锰酸盐指数来水浓度、溶解氧含量、流速和水深;与氨氮浓度变化率有关的关键因子为闸门开度、开启个数、氨氮来水浓度、溶解氧含量和p H值。