洪泽湖水体富营养化时空分布特征与影响因素分析

通过2014年—2017年对洪泽湖12个水质断面定期调查,采用营养状态指数(TLI)综合评价其水体富营养状态,同时应用主成分分析方法(PCA)分析其富营养化状态的时空变化特征。结果表明,洪泽湖70%以上的调查断面水质全年处于轻度富营养化状态,夏季是其富营养化最严重的季节;洪泽湖年内水体水质差异较大,而其水华特征并未呈现明显差异;洪泽湖富营养化很大程度上受制于营养盐的积累程度,并与湖泊透明度呈现极显著的负相关关系(p0.001),与湖水pH值呈现极显著的正相关关系。     

基于支持向量回归机的南黄海浒苔分布面积预测模型

绿潮作为一种新型的海洋灾害,已经引起了各个国家的重视.依据2012年南黄海海域浒苔遥感监测分布面积数据,选取了温度、天气状况、风向、风力、浪高5种影响浒苔扩散的气候因子,建立了基于SVR的浒苔分布面积预测模型,并与经典的最近邻点插值模型、线性插值模型、3次样条函数插值模型和分段3次Hermite插值模型进行了回归效果的对比.分析结果表明,基于SVR的浒苔分布面积预测模型能够为浒苔遥感数据的插补提供一种方法,且回归效果优于传统的回归方法,为浒苔的防治提供辅助决策信息.     

关于长江产业带建设总体布局的初步思考

重点开发长江是90年代中国经济重大战略布署。将长江产业带建设成具有强大经济实力的国家一级经济轴线,宜采用分层次推进与中心辐射相结合的发展战略,以浦东开发和三峡建设为契机,加强基础产业,发展新兴产业和第三产业,优化产业结构,以能源和交通建设先行,改善基础设施。同时,要协调产业带建设与浦东开发、三峡工程建设的关系。     

长江三峡柑桔的冻害和热害（二）

本文从柑桔冻害和热害的危害因子和指标等级划分的研究和选取入手,着重探讨了长江三峡地区(湖北境内)两害显著的时空变化特征、差异与关联性及对柑桔生产的影响;揭示了80年代以来冬暖春热的重大气候变化是使两害向“两极分化”的根本原因;讨论了三峡水利工程对两害时空格局的可能调整及减灾原理;最后提出了可能的对策。     

湖北省湿地的保护与利用

湿地是地球上具有多功能的、独特的生态系统，是人类最重要的生存环境之一。湖北省地处长江中游，湿地类型多，面积较大，河、湖湿地系统是主要的湿地类型。湖北湿地具有较大的资源潜力和环境调节功能，是自然界生物多样性丰富的生态景观。近年来，湖北省湿地保护面临人口增长的压力，围垦、污染和过度开发等对湿地保护构成了严重威胁，湿地环境遭到干扰和破坏。加强湿地科学的研究，保护管理好湖北湿地及其生态环境，实现湿地资源的持续利用，是湖北省2l世纪环保工作所面临的一项重要而紧迫的任务。     

神农架主峰南坡猕猴桃种质资源调查及保护策略

巴东县北部神农架主峰南坡的送子园原始森林保护区内具有种类繁多的猕猴桃种质资源，经调查发现共分布有中华猕猴桃（A.chiensis)、美味猕猴桃（A.deliciosa)、革叶猕猴桃(A．rubricalis var.coriacea)、葛枣猴桃(A．ploygama)、京梨猕猴桃(A．callosa var．henryi)、软枣猕猴桃(A．arguta)、巴东猕猴桃(A．tetramera var.badongenisis)、紫果猕猴桃(A．arguta var.purpurea)及紫果新变型、绵毛藤山柳(Clematoclthra lanosa)10种(包括变种、变型)。简述了各种类的植物学性状和果实经济性状，种质资源分布的主要特点以及生态环境，指出由于砍伐森林和环境条件的恶化使猕猴桃资源已受到威胁和破坏，提出保护策略的重点是提高全民的生态保护意识；可持续开发利用资源；加大科技对猕猴桃资源保护支撑的力度。其主要保育措施：一是在保护区内就地进一步加强物种全面保护；二是省级以上科研单位分区建立猕猴桃后种质资源圃，对濒危物种或持有物种进行迁地保护；三是开展超低温保存技术的研究，建立种子和花粉基因库。并建立完善与国际接轨的信息数据库平台，便于国际合作与交流。     

九龙江河口春季磷的形态分配及浮游植物对磷的响应

以石码河口及上游水域为研究对象，2007年5月对表层水中不同形态的磷及浮游植物生物量叶绿素a（Chla）进行了调查，分析河口磷形态分配的影响因素及与浮游植物生物量的关系。以颗粒态有机磷（POP）为主的颗粒态磷（PP）占总磷的61．2％；溶解态无机磷（DIP）占溶解态磷（TDP）的72．8％。河口区上游磷与河口磷的组成相似，雨水的淋洗作用对水体中磷的组成有较大影响，以颗粒态无机磷（PIP）的显著增高为特征。水中Chla与TP和DOP存在极显著的正相关，表明生物活动在一定程度上控制着该水域表层水中磷形态的分布。     

Biological Activity in a Heavily Organohalogen-Contaminated River Sediment (8 pp)

Background, Aims and Scope Sediments of the Spittelwasser creek are highly polluted with organic compounds and heavy metals due to the discharge of untreated waste waters from the industrial region of Bitterfeld-Wolfen, Germany over the course of more than one century. However, relatively few data have been published about the chloroorganic contamination of the sediment. This paper reports on the content of different (chloro)organic compounds with special emphasis on polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/F), and chlorobenzenes. Existing concepts for the remediation of Spittelwasser sediment include the investigation of natural attenuation processes, which largely depend on the presence of an intact microbial food web. In order to gain more insight in terms of biological activity, we analyzed the capacity of sediment microflora to degrade organic matter by measuring the activities of extracellular hydrolytic enzymes involved in the biogeochemical cycling of carbon, nitrogen, phosphorus and sulfur. Furthermore, the detection of physiologically active bacteria in the sediment, particularly of those known for their capability to reductively dehalogenate organochlorine compounds, illustrates the potential for intrinsic bioremediation processes. Methods PCDD/F and chlorobenzenes were analyzed by gas chromatography(GC)/mass spectrometry and GC/flame ionization detection, respectively. The activities of hydrolytic enzymes were determined from freshly sampled sediment layers using 4-methylumbelliferyl (MUF) or 7-amino-4-methylcoumarin-conjugated model compounds and kinetic fluorescence measurements. Physiologically active bacteria from different sediment layers were microscopically visualized by fluorescence in situ hybridization (FISH). Specific bacteria were identified by 16S rRNA gene amplification and sequencing. Results and Discussion The PCDD/F congener profile was dominated by dibenzofurans. In addition, the presence of specific tetra and pentachlorinated dibenzofurans supported the assumption that extensive magnesium production was one possible source for the high contamination. A range of other chloroorganic compounds, including several isomers of chlorobenzenes, hexachlorocyclohexane and 1,1,1-trichloro-2,2-bis (p-chloro-phenyl)ethane (DDT), was present in the sediment. Activities of extracellular hydrolytic enzymes showed a strong decrease in those sediment layers that were characterized by high contents of absorbable organic halogen (AOX), indicating disturbed organic matter decay. Interestingly, an abnormal increase of cellulolytic enzyme activities below the organochlorine-rich layers was observed, possibly caused by residual cellulose from discharges of sulfite pulping wastes. FISH revealed physiologically active bacteria in most sediment layers from the surface down to the depth of about 60 cm, including members of Desulfitobacterium (D.) and Sulfurospirillum. The presence of D. dehalogenans was confirmed by its partial 16S rRNA gene sequence. Conclusions Results of chemical sediment analyses demonstrated high loads of organochlorine compounds, particularly of PCDD/F. Several years after stopping the waste water discharge to Spittelwasser creek, this sediment remains a main source for pollution of the downstream river system by way of the ongoing mobilization of sediment during high floods. As indicated by our enzyme activity measurements, the decomposition potential for organic matter is low in organochlorine-rich sediment layers. In contrast, the comparably higher enzyme activities in less organochlorine-polluted sediment layers as well as the presence of physiologically active bacteria suggest a considerable potential for natural attenuation. Recommendations and Perspectives From our data we strongly recommend to explore the degradative capacity of sediment microorganisms and the limits for in situ activity towards specific sediment pollutants in more detail. This will give a sound basis for the integration of bioremediation approaches into general concepts to reduce the risk that permanently radiates from this highly contaminated sediment. Submission Editor: Dr. Henner Hollert (Henner.Hollert@urz.uniheidelberg.de)     

Treatability studies of naphthalene in soil,water and air with persulfate activated by iron(Ⅱ)

Chemical oxidation was applied to an artificially contaminated soil with naphthalene (NAP). Evaluation of NAP distribution and mass reduction in soil, water and air phases was carried out through mass balance. Evaluation of NAP distribution and mass reduction in soil, water and air phases was carried out through mass balance. The importance of the air phase analysis was emphasized by demonstrating how NAP behaves in a sealed system over a 4 hr reaction period. Design of Experiments method was applied to the following variables: sodium persulfate concentration [SP], ferrous sulfate concentration [FeSO₄], and pH. The system operated with a prefixed solid to liquid ratio of 1:2. The following conditions resulted in optimum NAP removal [SP] = 18.37 g/L, [FeSO₄] = 4.25 g/L and pH = 3.00. At the end of the 4 hr reaction, 62% of NAP was degraded. In the soil phase, the chemical oxidation reduced the NAP concentration thus achieving levels which comply with Brazilian and USA environmental legislations. Besides the NAP partitioning view, the monitoring of each phase allowed the variabilities assessment over the process, refining the knowledge of mass reduction. Based on NAP distribution in the system, this study demonstrates the importance of evaluating the presence of semi-volatile and volatile organic compounds in the air phase during remediation, so that there is greater control of the system as to the distribution and presence of the contaminant in the environment. The results highlight the importance of treating the contaminant in all its phases at the contaminated site.     

基于OMI数据的东南沿海大气臭氧浓度时空分布特征研究

基于臭氧监测仪(OMI)卫星反演数据,对2005—2018年东南沿海5省区域大气臭氧柱浓度数据进行提取及分析,探讨其时空分布格局及影响因素.结果表明:①在时间变化上,14年间,该区域大气臭氧柱浓度整体呈先上升后下降的趋势,2005—2013年臭氧柱浓度持续升高,最高值为324.52 DU,高值区不断向南部区域扩大;2013—2018年臭氧柱浓度呈下降趋势,最低值为228.27 DU,但在2017、2018年略有上升.②在空间分布上,臭氧柱浓度自北向南逐渐降低,高值区集中分布在江苏及浙江省北部;低值区集中于福建省南部及广东省大部分地区.③在季节变化上,大体呈现出春夏季高于秋冬季,高值区在春夏季交替出现,秋季略高于冬季,但差异不明显.④稳定性分析表明:研究区臭氧柱浓度整体呈现中部分散、南北部集聚、差异较显著的分布格局.⑤自然因素中,风向、气温均呈现显著正相关,江淮地区的梅雨季节(降水)及华南地区的台风和暴雨也起到显著作用.⑥人文因素中,臭氧柱浓度与地区生产总值、各产业生产总值及机动车保有量均表现出正相关,其中,臭氧柱浓度与第二产业的相关度最高.另外,臭氧柱浓度与NO_x排放量表现出显著相关性.VOC_s对臭氧柱浓度的影响中,工业源是主控因素,交通源和居民源次之,电厂源对臭氧柱浓度的影响最弱.这进一步说明臭氧浓度的变化受到了诸多因素的综合影响,但气温、NO_x及VOC_s的排放是臭氧浓度变化的主导因素.