京津冀区域霾天气特征

汇总京津冀区域内107个地面站的气象资料,利用14时实测的气象要素和天气现象资料对霾日进行判别,统计出各个站点1980~2008年中逐年及各月的霾日数.结果表明,北京、天津、河北霾天气整体变化趋势和波动特征较为相似,且均呈增加趋势,非城区站点平均霾日数明显呈增加趋势,且与市区站点霾日数的差距越来越小.京津冀区域霾日数的月际变化呈明显的双峰特征,即夏季和冬季霾日数较高.空间分布表明,霾日数高值区主要位于北京、天津、保定、石家庄、邯郸和邢台等地.多数站点霾日14时平均风速比非霾日低了1.0m/s以上,14时平均相对湿度则比非霾日高出20%以上.     

长江三角洲地区霾判别方法的对比分析

为对比霾判别方法的差异,探讨霾观测标准的再完善性,文中从空间分布与单点时间序列两方面分别分析研究了4种霾判别方法的特征与适用性.选取中国长江三角洲地区1980~2009年38个地面观测站的气象资料,根据使用日均值的方法 1、2和使用14:00观测值的方法 3分别统计各站点的霾日,分析3种方法的异同.发现这些方法都能够反映出霾的长期变化趋势,但存在差异,这种差异随着年代际变化逐渐减小.由方法 1得到的霾日数最多,方法 3考虑了天气现象,比方法 1和2更合理.依据南京北郊2012年5月~2013年4月的逐时PM2.5浓度、相对湿度和能见度等资料,分析比较了方法 4(霾的观测和等级预报,QX/T 113-2010)与方法 1、2、3的不同.结果表明,由方法 3统计出的霾日少于其他方法,由方法 4统计出的霾日数介于方法 1与方法 3的结果;方法 3不能分辨出霾的严重程度,而其他方法能较好地分辨出霾的严重程度.     

常州市霾天气特征及其影响因子分析

基于常州市气象观测站2001-2013年的气象资料和大气自动站2009-2013年的监测数据,对常州市霾天气的变化特征、成因及其影响因子进行了初步分析。结果表明：2001-2013年,霾日数在全年及四季都呈现逐渐增多的年际变化特征,其中在2001-2008年,霾日数的趋势平稳且窄幅波动,但2009-2013年,霾日数急剧增加。季节变化上表现出夏季少、冬季多的分布特征。霾天气多发生在午后,11时出现的次数最多。常州霾天气持续日数不断增加,2013年连续霾日最长是16 d。常州霾典型天气形势为受冷高压或变性冷高压控制之下和处于入海高压后部或底部。常州霾天气受气象因子的影响,在静风、偏东风、50％～60％的相对湿度、逆温、降水偏少和大气湍流不利气象扩撒条件下都易形成霾。     

三种霾日统计方法的比较分析

为了研究单次值法、日均值法、14时值法3种常用的霾日和轻雾(雾)日统计结果的异同,以环首都圈京津冀晋四省市为例进行了比较.华北地区霾日用3种方法统计的过去60余年霾日的区域分布表明,3种方法统计的霾日是单次值法>日均值法>14时值法,大致是1:0.54:0.45的关系,但区域分布趋势比较相似.典型城市霾日的长期变化趋势大都十分相似.而轻雾(雾)日的长期变化趋势表明,用单次值法统计的明显偏多,且有长期下降趋势;而用日均值法与14时值法统计的轻雾(雾)日无大差别,且没有明显的长期变化趋势,反映了年季和年代季的气候波动.从长期季节变化趋势来看,3种统计方法的结果除日数的差别外,季节分布特征比较类似.一个突出的特点是除去采暖季有较多的霾日外,在盛夏季节霾日也明显多,集中出现在6~9月,尤其是7~8月,与桑拿天同期出现,这与全国大部分城市的变化趋势完全不同.是华北地区的特有现象.用单次值法统计霾日,将包括所有的霾过程,即大范围持续时间长,且与一定天气系统与近地层扩散条件相关连的霾,及在稳定的晴朗夜间由于辐射降温,使相对湿度升高而导致能见度下降形成的霾.用日均值法,则可能更多的显示长时间大范围的霾天气过程;而使用14时法,则对早晚因湿度增加降低能见度出现的霾天气漏记,突出长时间大范围的霾天气过程.     

三种观测标准的霾日与空气污染日对比分析

目前气象观测业务和空气污染分析中存在对霾日统计的分歧,甚至出现空气污染日无霾的现象,对霾观测标准的科学划分,显得非常重要和紧迫。利用2013—2015年廊坊市气象观测站能见度、相对湿度、霾人工观测资料和廊坊市环保局AQI、PM25浓度等气象环保资料,对目前观测业务和空气污染分析中常用的三种霾观测、统计方法进行了对比分析。分析发现:目前廊坊气象观测站所依据的记录霾天气现象的标准,与实际大气污染相趋甚远,不能反映实际的空气污染状况,建议国家及省级相关部门及早根据实际情况,更新霾观测标准,更好地为当前大气污染的防治工作提供客观依据。     

三种霾日统计方法的比较分析——以环首都圈京津冀晋为例

为了研究单次值法、日均值法、14时值法3种常用的霾日和轻雾(雾)日统计结果的异同,以环首都圈京津冀晋四省市为例进行了比较.华北地区霾日用3种方法统计的过去60余年霾日的区域分布表明,3种方法统计的霾日是单次值法日均值法14时值法,大致是1:0.54:0.45的关系,但区域分布趋势比较相似.典型城市霾日的长期变化趋势大都十分相似.而轻雾(雾)日的长期变化趋势表明,用单次值法统计的明显偏多,且有长期下降趋势;而用日均值法与14时值法统计的轻雾(雾)日无大差别,且没有明显的长期变化趋势,反映了年季和年代季的气候波动.从长期季节变化趋势来看,3种统计方法的结果除日数的差别外,季节分布特征比较类似.一个突出的特点是除去采暖季有较多的霾日外,在盛夏季节霾日也明显多,集中出现在6~9月,尤其是7~8月,与桑拿天同期出现,这与全国大部分城市的变化趋势完全不同.是华北地区的特有现象.用单次值法统计霾日,将包括所有的霾过程,即大范围持续时间长,且与一定天气系统与近地层扩散条件相关连的霾,及在稳定的晴朗夜间由于辐射降温,使相对湿度升高而导致能见度下降形成的霾.用日均值法,则可能更多的显示长时间大范围的霾天气过程;而使用14时法,则对早晚因湿度增加降低能见度出现的霾天气漏记,突出长时间大范围的霾天气过程.     

四川盆地霾天气变化特征和典型霾过程分析

选用盆地1973-2013年12个气象站的资料,在定义一个适合四川盆地的霾天气识别标准的基础上,分析了四川盆地霾天气的变化特征。并对2013年2月的一次典型霾天气演变过程进行分析,探究霾天气的形成与其它气象因素的关系。结果表明,四川盆地近41 a总平均年霾日为97 d,没有明显的长期变化趋势,但是霾天气的变化可分为3个阶段,第一阶段为1973-1988年,盆地的平均年霾日为90 d,变化趋势为每10 a增加32 d。第2阶段为1989-1999年,平均年霾日可达112 d,没有明显变化趋势。第3阶段为2000-2013年,平均年霾日为95 d,变化趋势为每10 a减少12 d。四川盆地以30°N为界,南部为霾天气多发区域。在霾日的季节分布中,冬季最多,其次是春秋季,夏季最少,而且近40多a来夏季的霾日有增加的趋势。通过个例分析发现,霾天气的产生受低风速的影响最大,相反消散过程中近地面和对流层中层的风速都较高。霾天气发生时大气层结偏稳定,盆地冬天近地面普遍存在逆温现象现象,出现霾天气时逆温层强度明显较高。     

中山市2000~2014年霾天气特征及气象影响因子

利用中山市2000~2014年气象资料及2013~2014年环境监测站资料,分析中山市霾特征及气象影响因子,结果表明,中山市霾日数年际变化明显,最少为11d,出现在2005年;最多为134d,出现在2008年.霾天气主要发生在秋冬季节,霾日数最多的月份是1月,平均为10.5d.霾日PM_2.5的平均浓度是非霾日的2.26倍,PM_2.5是霾天气的重要污染物.中山市霾日典型天气形势有7种:大陆高压型、海上高压型、均压场型、冷锋前部型、台风外围下沉气流型、槽前脊后型、低压槽型.其中以大陆高压型占比例最高,为52.03%,冷锋前部型造成的能见度最低.气流轨迹聚类分析表明,影响中山的气流轨迹有7类,主要来源于东北方向的大陆和偏东方向的沿海;在东北方向气流轨迹影响下,污染物浓度较高;在东部沿海的气流轨迹下,能见度较低,表明中山市的霾天气受区域传输影响显著.     

不同判别方法下四川霾日的气候变化特征

根据近34年(1981—2014年)156个四川地面站的地面观测资料,对比分析了在3种霾日判别方法下霾日的空间分布、季节变化、年代际变化特征以及气候趋势系数的分布特征.利用Morlet小波分析法比较了霾日的周期变化特点.结果表明:1原始观测霾日集中于四川盆地的北部;方法一霾日集中于盆地中南部和东部;方法二霾日集中于盆地地区,无代表高值区;方法三分布类似于方法一.2在季节变化上:不同判别方法下霾日的季节变化类似,秋冬霾日多于春夏.3霾日年代际变化明显.原始观测霾日2013年始出现突增;方法二霾日从2001年始有明显增长;方法一与方法三的年代际变化特征相似.4气候趋势系数上:原始观测变化特征不明显;方法一的系数呈现出南北反向变化;方法二与方法一的分布相似;方法三中系数的正负值区较为集中.5小波变化上:原始观测中霾日无明显周期变化,判别方法一、二、三均有各自的周期变化特点.     

近50年华中地区霾污染的特征

基于1962~2011年霾日观测资料,使用线性回归、聚类分析及相关分析等统计方法分析了近50年华中地区霾污染的时空变化特征及其成因.结果表明,华中地区的霾高发中心位于河南中北部、湖北中西部和湖南中部人口集中的气溶胶浓度高值区,其中霾日数最多的站点为河南新乡,年均达到79.1d.霾的季节性变化表现为冬季霾日数最多,夏季最少,霾污染是典型的冬季大气环境事件.但随着近年春夏秋三季霾日的增加,华中地区霾污染的季节性差异减小.城市地区是华中霾污染严重的区域.近50年污染地区霾发生频率增多,而相对清洁地区霾污染发生频率减少.华中地区大气环境呈现出两极分化的变化特征.近50年来华中地区霾日增加受人为污染物排放加强和东亚季风减弱的共同影响.     

Toxic effects of acetochlor, methamidophos and their combination on nifH gene in soil

Toxic effects of two agrochemicals on nifH gene in agricultural black soil were investigated using denaturing gradient gel electrophoresis （DGGE） and sequencing approaches in a microcosm experiment. Changes of soil nifH gene diversity and composition were examined following the application of acetochlor, methamidophos and their combination. Acetochlor reduced the nifH gene diversity （both in gene richness and diversity index values） and caused changes in the nifH gene composition. The effects of acetochlor on nifH gene were strengthened as the concentration of acetochlor increased. Cluster analysis of DGGE banding patterns showed that nifH gene composition which had been affected by low concentration of acetochlor （50 mg/kg） recovered firstly. Methamidophos reduced nifH gene richness that except at 4 weeks. The medium concentration of methamidophos （150 mg/kg） caused the most apparent changes in nifH gene diversity at the first week while the high concentration of methamidophos （250 mg/kg） produced prominent effects on nifH gene diversity in the following weeks. Cluster analysis showed that minimal changes of nifH gene composition were found at 1 week and maximal changes at 4 weeks. Toxic effects of acetochlor and methamidophos combination on nifH gene were also apparent. Different nifH genes （bands） responded differently to the impact of agrochemicals： four individual bands were eliminated by the application of the agrochemicals, five bands became predominant by the stimulation of the agrochemicals, and four bands showed strong resistance to the influence of the agrochemicals. Fifteen prominent bands were partially sequenced, yielding 15 different nifH sequences, which were used for phylogenetic reconstructions. All sequences were affiliated with the alpha- and beta-proteobacteria, showing higher similarity to eight different diazotrophic genera.     

EDTA-enhanced phytoremediation of lead contaminated soil by Bidens maximowicziana

Phytoremediation is a potential cleanup technology for the removal of heavy metals from contaminated soils.Bidens maximowicziana is a new Pb hyperaccumulator,which not only has remarkable tolerance to Pb but also extraordinary accumulation capacity for Pb.The maximum Pb concentration was 1509.3 mg/kg in roots and 2164.7 mg/kg in overground tissues.The Pb distribution order in the B. maximowicziana was:leaf>stem>root.The effect of amendments on phytoremediation was also studied.The mobility of soil Pb and the Pb concentrations in plants were both increased by EDTA application.Compared with CK(control check),EDTA application promoted translocation of Pb to overground parts of the plant.The Pb concentrations in overground parts of plants was increased from 24.23-680.56 mg/kg to 29.07-1905.57 mg/kg.This research demonstrated that B.maximowicziana appeared to be suitable for phytoremediation of Pb contaminated soil,especially,combination with EDTA.     

Distribution and ecological effect of mercury in Laogang landfill, Shanghai, China

Laogang landfill near Shanghai is the largest landfill in China, and receives about 10000 t of daily garbage per day, Samples of topsoil and plants were analyzed to evaluate mercury pollution from the landfill. For topsoil samples, there were significant correlations among total mercury （HgT）, combinative mercury （Hgc） and gaseous mercury （HgG）, and content of total organic carbon （TOC）, but, no significantly relationship was found between Hg content and filling time. Hg content changes in vertical profiles with time showed that the average Hgv of profiles 1992, 1996, and 2000 was similar, but their average HgG was quite different. HgT was significantly correlated with Hgc in profile 1992 and 2000, and Hgv was significantly correlated with Hg6 in profile 1996. HgG/Hgv ratio in profile samples decreased in the order of （HgG,/HgT）1992〉（HgG/HgT）1996〉〉（HgG/HgT）2000. A simple outline of Hg release in landfill could be drawn： with increasing of filling time, degradation undergoes different biodegradation, accordingly, gaseous mercury goes through small, more, and small proportion to total mercury. Distribution of Hg in plants was inhomogeneous, following the order of leaf〉root〉stem. The highest value of leaf may be associated with higher atmospheric Hg from landfill. Ligneous plants （e.g. Phyllostachys glanca, Prunus salicina and Ligustrum lucidum） are capable of enriching more Hg than herbaceous plants.     

Arsenic uptake by arbuscular mycorrhizal maize （Zea mays L.） grown in an arsenic-contaminated soil with added phosphorus

The effects of arbuscular mycorrhizal (AM) fungus (Glomus mosseae) and phosphorus (P) addition (100 mg/kg soil) on arsenic (As) uptake by maize plants (Zea mays L.) from an As-contaminated soil were examined in a glasshouse experiment.Non-mycorrhizal and zero-P addition controls were included.Plant biomass and concentrations and uptake of As,P,and other nutrients,AM colonization,root lengths,and hyphal length densities were determined.The results indicated that addition of P significantly inhibited root colonization and development of extraradical mycelium.Root length and dry weight both increased markedly with mycorrhizal colonization under the zero-P treatments,but shoot and root biomass of AM plants was depressed by P application.AM fungal inoculation decreased shoot As concentrations when no P was added,and shoot and root As concentrations of AM plants increased 2.6 and 1.4 times with P addition,respectively.Shoot and root uptake of P,Mn,Cu,and Zn increased,but shoot Fe uptake decreased by 44.6%,with inoculation, when P was added.P addition reduced shoot P,Fe,Mn,Cu,and Zn uptake of AM plants,but increased root Fe and Mn uptake of the nonmycorrhizal ones.AM colonization therefore appeared to enhance plant tolerance to As in low P soil,and have some potential for the phytostabilization of As-contaminated soil,however,P application may introduce additional environmental risk by increasing soil As mobility.     

Enzymatic oxidation of aqueous pentachlorophenol

The influence of the nonionic surfactant Tween 80 on pentachlorophenol （PCP） oxidation catalyzed by horseradish peroxidase was studied. The surfactant was tested at concentrations below and above its critical micelle concentration （CMC）. Enhancement of PCP removal was observed at sub-CMCs. The presence of Tween 80 in the reaction mixture reduced enzyme inactivation which occurred through a combination of free radical attack and sorption by precipitated products. A simple first-order model was able to simulate time profiles for enzyme inactivation in the presence or absence of Tween 80. At supra-CMCs, the surfactant caused noticeable reductions in PCP removal, presumably through micelle partitioning of PCP which precluded the hydrophobic PCP molecule from interacting with the enzyme.     

Decomposition of alachlor by ozonation and its mechanism

Decomposition and corresponding mechanism of alachlor, an endocrine disruptor in water by ozonation were investigated. Results showed that alachlor could not be completely mineralized by ozone alone. Many intermediates and final products were formed during the process, including aromatic compounds, aliphatic carboxylic acids, and inorganic ions. In evoluting these products, some of them with weak polarity were qualitatively identified by GC-MS. The information of inorganic ions suggested that the dechlorination was the first and the fastest step in the ozonation of alachlor.     

Degradation of metabolites accumulated of benzo[a]pyrene by coupling Penicillium Chrysogenum with KMnO4

Several main metabolites of benzo[a]pyrene （BaP） formed by Penicillium chrysogenum, Benzo[a]pyrene-1,6-quinone （BP 1,6- quinone）, trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene （BP 7,8-diol）, 3-hydroxybenzo[a]pyrene （3-OHBP）, were identified by high-performance liquid chromatography （HPLC）. The three metabolites were liable to be accumulated and were hardly further metabolized because of their toxicity to microorganisms. However, their further degradation was essential for the complete degradation of BaP. To enhance their degradation, two methods, degradation by coupling Penicillium chrysogenum with KMnO4 and degradation only by Penicillium chrysogenum, were compared; Meanwhile, the parameters of degradation in the superior method were optimized. The results showed that （1） the method of coupling Penicillium chrysogenum with KMnO4 was better and was the first method to be used in the degradation of BaP and its metabolites; （2） the metabolite, BP 1,6-quinone was the most liable to be accumulated in pure cultures; （3） the effect of degradation was the best when the concentration of KMnO4 in the cultures was 0.01% （w/v）, concentration of the three compounds was 5 mg/L and pH was 6.2. Based on the experimental results, a novel concept with regard to the bioremediation of BaP-contaminated environment was discussed, considering the influence on environmental toxicity of the accumulated metabolites.     

Impact of atrazine and nitrogen fertilizers on the sorption of chlorotoluron in soil and model sorbents

Sorption of chlorotoluron in ammonium sulfate, urea and atrazine multi-solutes system was investigated by batch experiments. The results showed application of nitrogen fertilizers to the soil could affect the behavior of chlorotoluron. At the same concentration of N, sorption of chlorotoluron decreased as the concentration of atrazine increased on the day 0 and 6 in soil, respectively. The sorption of chlorotoluron increased from 0 to 6 d when soils were preincubated with deionized water, ammonium sulfate and urea solution for 6 d. That indicated incubation time was one of the most important factors for the sorption of chlorotoluron in nitrogen fertilizers treatments. The individual sorption isotherms of chlorotoluron in rubbery polymer and silica were strictly linear in single solute system, but there were competition sorption between pesticides or between pesticides and nitrogen fertilizers. That indicated the sorption taken place by concurrent solid-phase dissolution mechanism and sorption on the interface of water-organic matter or water-mineral matter.     

基于综合水质标识指数和对应分析法的校园河道水质评价

以三峡大学的校园河道求索溪为研究对象,利用综合水质标识指数法确定求索溪水质类别,分析其水质时空变化规律,并利用对应分析法得出求索溪中不同监测点的主要污染因子.研究结果表明:求索溪整体的综合水质标识指数为7.423,整体水质为劣V类(地表水环境质量标准GB 3838-2002)且黑臭.从时间变化来看,求索溪4月份的水质最差,5月份次之,4、5月份所有监测点的水质都劣于V类且黑臭;8月份水质最好,水质为Ⅳ类;从空间分布来看,8个监测点综合水质标识指数均超过6.0,水质为劣V类,其中6号监测点的水质相对最好,监测点3号的水质相对最差;对应分析法得出求索溪的整体水体污染程度受总氮因子的影响最大,其次为总磷.该研究拟为求索溪及类似校园河道的水环境治理研究提供基础依据和参考.     

Potential of plant polyphenol oxidases in the decolorization and removal of textile and non-textile dyes

In this study an effort has been made to use plant polyphenol oxidases; potato （Solanum tuberosum） and brinjal （Solanum melongena）, for the treatment of various important dyes used in textile and other industries. The ammonium sulphate fractionated enzyme preparations were used to treat a number of dyes under various experimental conditions. Majority of the treated dyes were maximally decolorized at pH 3.0. Some of the dyes were quickly decolorized whereas others were marginally decolorized. The initial first hour was sufficient for the maximum decolorization of dyes. The rate of decolorization was quite slow on long treatment of dyes. Enhancement in the dye decolorization was noticed on increasing the concentration of enzymes. The complex mixtures of dyes were treated with both preparations of polyphenol oxidases in the buffers of varying pH values. Potato polyphenol oxidase was significantly more effective in decolorizing the dyes to higher extent as compared to the enzyme obtained from brinjal polyphenol oxidase. Decolorization of dyes and their mixtures, followed by the formation of an insoluble precipitate, which could be easily removed simply by centrifugation.