程海冬季水华暴发期间氮、磷营养元素的形态与分布

氮、磷营养元素是湖泊生态系统中极其重要的生态因子,它们以不同形态存在于湖泊水体中,表现出不同的地球化学行为和生态效应,从而支配着湖泊生态系统的生产力水平和湖泊富营养化进程。通过设置3个断面9个采样站14个采样点,研究了程海湖水体中氮、磷营养元素的形态与分布,结果表明：2009年11月23日—2010年2月20日,以铜绿微囊藻（Microcystis aeruginosa Kutz.）为主的程海冬季水华暴发期间,总氮质量浓度0.540~3.906 mg.L-1,平均0.836 mg.L-1;总磷质量浓度0.036~0.166 mg.L-1,平均0.061 mg.L-1。其中,溶解态氮、溶解态磷分别为61.7%和50.8%。溶解态氮以有机氮为主,溶解态磷则以无机磷为主。水华期间生物可直接利用氮质量浓度0.118 mg.L-1;生物可直接利用磷质量浓度0.021 mg.L-1,分别占总氮、总磷质量浓度的14.1%和34.4%,显示出此特定时期,氮的消耗速度较磷快。氮素、磷素及其赋存形态在程海的时间分布上有不同的节奏;水平分布差异不明显;垂直分布在水表层至亚底层的水柱中差异也不明显,而在湖底层最高。     

我国海水水质基准的构建:以三丁基锡为例

我国近岸海域污染形势严峻、污染物种类繁多、生态健康风险复杂,现有的海水水质标准难以满足当前海洋环境污染评价、管理和监控的需求,亟需适宜我国海洋区系特征的海水水质基准作为水质标准修订与制定的理论依据.借鉴美国、欧盟和荷兰等国家水质基准的制定方法,提出了构建我国海水水质基准的思路,并给出了数值型双值基准的数据要求、定值方法和相应的计算模式等.以三丁基锡化合物(TBT)为例,按照论文建立的方法,计算了保护我国海洋水生生物的TBT基准.结果表明:我国TBT化合物海水水质基准高值(HSWC)和海水水质基准低值(LSWC)分别为0.43μg·L-1和0.002μg·L-1,与美国,加拿大和英国等国家的推荐基准值略有不同.研究结果将为我国海水水质基准的制定与研究提供帮助.     

分岔隧道火灾火源位置对临界风速影响的数值模拟分析

为探究分岔隧道火灾火源位置对临界风速的影响规律,使用数值模拟方法对火源位于分岔隧道分岔口前和分岔口后的火灾场景下的临界风速进行研究.研究结果表明:火源位于分岔口后的主隧道时,临界风速明显大于火源位于分岔口前的临界风速;在一定范围热释放速率下,分岔隧道临界风速与热释放速率的1/3次方成正比;在分岔隧道模型中,相同热释放速...     

基于活性微生物特征的供水管壁生物膜生长特性

管网生物膜由各种活性微生物、微生物残体及有机无机杂质组成,管网生物膜的生长会导致机会致病菌寄居、管道腐蚀以及水质恶化等系列饮用水卫生问题.为研究供水管壁生物膜形成过程和附着生长活性微生物的分布特征,采用异养菌平板计数(HPC)、流式细胞术(FCM)和16S rRNA高通量测序对3种典型室内供水管材:聚氯乙烯(PVC)、无规共聚聚丙烯(PPR)、不锈钢(STS)内壁活性微生物的生长特性和群落多样性进行了分析.结果表明,PVC管壁生物量在第73 d最先达到峰值,3种管材内壁单位面积最大生物量、生物膜成熟时期生物量均呈现PVC PPR STS的规律. 3种管材表面活性细菌群落结构组成上,PVC管表面主要以硝化螺旋菌门为主,PPR和STS管以疣微菌门为主,其中STS管壁上生物膜物种丰富度最低、多样性最小,群落结构最简单. PVC和PPR管内壁表面相较STS管存在更多的蓝藻细菌和放线菌,在饮用水输配过程中更易引发饮用水嗅味问题.管材介质对管壁生物膜上微生物群落结构存在一定影响.     

Influence of haze pollution on water-soluble chemical species in PM2.5 and size-resolved particles at an urban site during fall

To investigate the influence of haze on the chemical composition and formation processes of ambient aerosol particles,PM_(2.5) and size-segregated aerosol particles were collected daily during fall at an urban site of Gwangju,Korea.During the study period,the total concentration of secondary ionic species(SIS) contributed an average of 43.9% to the PM_(2.5) ,whereas the contribution of SIS to the PM_(2.5) during the haze period was 62.3%.The NO_3 and SO~(2-)_4 concentrations in PM_(2.5) during the haze period were highly elevated,being 13.4 and 5.0 times higher than those during non-haze period,respectively.The PM,NO~-_3,SO~(2-)_4,oxalate,water-soluble organic carbon(WSOC),and humic-like substances(HULIS) had tri-modal size distributions peaks at 0.32,1.0,and 5.2 μm during the non-haze and haze periods.However,during the non-haze period they exhibited dominant size distributions at the condensation mode peaking at 0.32 μm,while on October 21 when the heaviest haze event occurred,they had predominant droplet mode size distributions peaking at 1.00 μm.Moreover,strong correlations of WSOC and HULIS with SO~(2-)_4,oxalate,and K+at particle sizes of 1.8 μm indicate that secondary processes and emissions from biomass burning could be responsible for WSOC and HULIS formations.It was found that the factors affecting haze formation could be the local stable synoptic conditions,including the weak surface winds and high surface pressures,the long-range transportation of haze from eastern China and upwind regions of the Korean peninsula,as well as the locally emitted and produced aerosol particles.     

A System for Measuring Vertical Concentration Profiles of Gaseous Pollutants,Using Carbon Dioxide as a Case Study

An electronically-controlled sampling system, characterised by its organ pipe design, has been developed for sampling air sequentially, at different heights within the breathing zone. Data are automatically logged at the different receptor levels, for the determination of the average vertical concentration profile of gaseous pollutants. The system has been coupled to a carbon dioxide monitor and used in a brief study of the spatial and temporal variation of indoor carbon dioxide concentration. The system can easily be extended for different heights or modified for use with other types of gas monitor. The results of a trial run, which was carried out in a coffee room, are presented and applications of the Organ Pipe Sequential Sampling (OPSS) system are discussed.     

An Analysis of the Wind Energy Potential of Elazig,Turkey

Abstract

In this study, the wind energy potential of Elazig is statistically analyzed based on hourly measured wind speed data over the five-year period from 1998 to 2002. The probability density distributions are derived from cumulative distribution functions. Two probability density functions are fitted to the measured probability distribution on a yearly basis. The wind energy potential of the location is studied based on the Weibull and Rayleigh distributions. It was found that the numerical values of both Weibull parameters (k and c) for Elazig vary over a wide range. The yearly values of k range from 1.653 to 1.878 with an average value of 1.819, while those of c are in the range of 2.757–2.994 m/s with an average value of 2.824 m/s. In addition, yearly mean wind speed and mean power density of Elazig is found as 2.79 m/s and 38.76 W/m², respectively. The wind speed distributions are represented by Weibull distribution and also by Rayleigh distribution, with a special case of the Weibull distribution for k = 2. As a result, the Rayleigh distribution is found to be suitable to represent the actual probability of wind speed data for Elazig.     

偏远地区大气中持久性有机污染物研究进展

持久性有机污染物(POPs)在偏远地区大气中的分布与迁移已经成为大气POPs研究的热点.基于被动采样技术的大尺度POPs监测网络已经应用于偏远地区大气POPs的研究之中.其研究成果显示,最近50～60年以来,大气中POPs浓度的最大峰值出现在80年代左右,而80年代之后大气中POPs的浓度日趋减小.这说明各国陆续禁用POPs之后,大气中POPs的浓度有显著降低的趋势.受温度和季节性使用的影响,大气POPs的浓度呈现明显的季节性变化特点:有机氯农药的浓度主要表现为夏季高而冬季低;多环芳烃的浓度则主要表现为冬季高而夏季低.基于POPs高挥发性和长距离大气传输的特点,POPs可以在全球范围内广泛分布,而高海拔地区由于气温较低,使其相对于低海拔地区成为了POPs的"接收器".大气POPs分布和迁移受温度、降水、气候事件的影响.而且POPs在大气与不同下垫面之间的界面交换的方向、速度和通量也主要受环境温度和POPs的挥发能力的制约.综合大气POPs迁移与气候因素、界面特点之间的关系建立了多介质、大尺度的大气POPs归趋模型.模型的建立和POPs来源的明确使大气POPs传输机制的研究逐渐深入.此外还讨论了目前大气POPs研究中存在着的一些亟待解决的问题,并提出该领域未来可能的发展趋势.     

黄海近岸表层沉积物中PAHs的分布特征与潜在风险

利用第二次全国海洋污染基线调查数据,考察了我国黄海近岸海域表层沉积物中多环芳烃(PAHs)的分布状况、组成比例,并开展了初步的来源分析和潜在生态风险评价.研究结果表明,PAHs的含量范围从未检出至8294 ng·g-1,高值站点主要位于辽东半岛的大连湾附近海区,以及山东半岛北部的威海沿岸.在辽东半岛、山东半岛的近岸海区,表层沉积物中的PAHs以中、高环(4～5环)组分占据明显优势;而在江苏近岸海区,低环组分(2～3环)的比例明显上升.低环与中高环组分的相对丰度以及成对同分异构体的比值结果显示,各海区表层沉积物中PAHs的主要来源是各类燃烧释放过程,如燃煤、生物质、天然气和交通尾气等,石油产品输入的影响居次要地位.依据效应低值区间ERL的警戒水平,计算ERL商的平均值,从而初步得到各海区潜在的PAHs生态风险水平.结果表明,大连湾PAHs污染较为严重,各PAHs组分的浓度均高于ERL警戒水平,而苯并(a)芘甚至超出效应中值区间的境界水平ERM,显示大连湾近岸海区具有较高的PAHs生态风险,而其它海区的潜在生态风险则较低.     

孔径分布和溶液浓度对碳气凝胶电极电吸附除盐性能的影响分析

在不同进水浓度下,采用两种比表面积相似但是孔径分布不同的碳气凝胶作为电极进行了一系列电吸附除盐平衡试验.结果表明,随着溶液浓度的变化,不同的孔径分布对碳气凝胶除盐效果影响不一样.其机理为双电层的存在,使得碳气凝胶空隙内的双电层扩散层相互叠加;同时,根据德拜定律,碳气凝胶空隙内的双电层扩散层在不同浓度溶液中厚度不同,从而使得双电层扩散层相互叠加的情况也随浓度变化而变化.这两种作用共同导致了实验结果.当溶液浓度为 0.01 mol·L-1时,选择主要孔径不小于20hm的碳气凝胶电极;当溶液浓度为 0.1 mol·L-1时,应选用主要孔径不小于 10nm 的材料;当溶液浓度为几 mol·L-1时.则分散层几乎消失,孔径大小对电吸附性能影响几乎不考虑.