生态文明建设的关键因素识别

生态文明建设是共创民族伟业、中国圆梦的时代重任,提高生态文明建设水平需要对生态文明建设的关键因素进行分析识别。本文从生态文明意识、生态文明制度和生态文明行为三个方面建立生态文明建设影响因素指标体系,选取全国31个省份2012至2014年的相关数据,运用BP神经网络法降低DEMATEL模型中专家打分建立关联矩阵的主观性,结合摆幅置权法(SW)得出综合重要度,遴选出生态文明建设关键因素。其中,年份最近的2014年计算得出的关键因素按照重要度排序依次为:本级环保能力建设资金使用总额、排污费解缴入库户金额、机动车污染物排放总颗粒物、网站主动公开各类政府环境信息条数和环保系统人员总数。将这些因素按照生态文明的基本内涵划分为三大类,得到3点结论:生态意识虽不起决定性作用,但能强化整个社会的生态文明建设的思想和理念,生态文明意识所占的比例先降后升,不断提高;随着生态文明建设理论和实践经验的丰富,逐渐感受到成熟的制度设计、明确的制度规范才是根本,生态文明制度类别在关键因素中所占的比例越来越高;生态文明行为作为表现形式,随着其他两方面的变化,生态文明行为不断改善,在生态文明建设的关键因素中所占比例下降。本文在生态文明意识方面提出要针对性地帮助和鼓励各级环保部门开展信息公开工作;在生态文明制度方面提出强化环保能力建设资金的监管力度,发挥排污费的真正作用,提升环保系统人员的能力素养,探索新工作思路等举措;在生态文明行为方面提出综合车、油、路等多方面措施防治机动车排放污染等建议。     

大连地区唐氏筛查孕中期妇女羊水中甲状腺激素水平与PBDEs内暴露关系初探

多溴联苯醚(polybrominated diphenyl ethers,PBDEs)是一类常用的溴代阻燃剂,由于使用广泛,已成为普遍存在的环境污染物。研究表明,PBDEs具有内分泌干扰作用,影响甲状腺功能,对胚胎发育、婴幼儿及儿童的健康存在潜在的危害。本研究采集了100例具羊水穿刺指征的孕妇的孕中期羊水样本,采用罗氏全自动电化学发光免疫分析仪测定羊水中促甲状腺激素(TSH)、三碘甲状腺原氨酸(TT3)、游离三碘甲状腺原氨酸(FT3)、甲状腺素(TT4)、游离甲状腺素(FT4)、抗甲状腺过氧化酶抗体(TPOA)和抗甲状腺球蛋白抗体(TGA)的含量,用气相色谱-负化学源-质谱法测定羊水样品中16种PBDEs同系物含量。结果显示,羊水中TSH、TT3、FT3、TT4、FT4中位数分别为0.342μIU·m L-1、0.949 nmol·L-1、1.52 pmol·L-1、11.02 nmol·L-1和3.91pmol·L-1,95%参考区间值分别为0.174~0.872μIU·m L-1、0.835~1.01 nmol·L-1、1.26~2.72 pmol·L-1、9.42~20.68 nmol·L-1和2.16~6.35 pmol·L-1。具有唐氏筛查高风险和甲状腺激素水平低下的羊水样品中共检出6种BDEs(BDE-47、BDE-71、BDE-138、BDE-183、BDE-190、BDE-209),其中BDE-71、183和190在被检羊水样品中均被检出,并且,TSH水平低下的羊水中BDE-190和209负荷水平显著高于正常组。这些结果提示,大连地区孕中期妇女羊水存在PBEDs内暴露,并且PBDEs内暴露可能与羊水的甲状腺激素水平低下、尤其TSH水平升高有关,提示PBDEs暴露可能与胎儿中枢神经系统损伤产生的下丘脑-垂体-甲状腺(HPT)轴功能失调有关。因此,羊水PBDEs内暴露对新生儿出生结局的影响值得进一步关注。     

某石化废水的综合毒性评价及其处理工艺对毒性的削减规律研究

利用生物毒性测试对环境中的污染物进行生态风险评价,是目前风险评价中的研究热点。本研究以明亮发光杆菌(Photobacterium phosphoreum)、斜生栅藻(Scenedesmus obliquus)和大型溞(Daphina magna)为受试生物,对某石化厂废水的处理流程中5个主要单元出水的急性毒性进行了测试,分析了其急性毒性与理化指标间的相关性;同时,为了解不同处理单元毒性去除效果及主要毒性来源,结合毒性鉴别评价(toxicity identification evaluation,TIE)技术对各阶段出水的毒性削减及其主要致毒物质类别进行了分析。毒性测试结果表明,该废水处理厂对石化废水的毒性去除效果比较显著,其中进水对明亮发光杆菌、斜生栅藻和大型溞分别表现为中毒、高毒和剧毒,最终处理后出水的毒性分别为无急性毒、中毒和微毒,对毒性的去除效率分别为96.4%、74.3%和99.5%。TIE结果表明,石化废水中的主要致毒物质是非极性有机物和可滤型物质。本研究结果为石化废水的综合生物毒性评价提供了研究基础,为探讨废水生物毒性的去除提供了实例参考。     

环氟菌胺的水解动力学研究

为明确环氟菌胺的水解动力学规律,采用室内模拟试验方法,探究了温度、p H值、表面活性剂和不同种类水体对环氟菌胺水解的影响。结果表明:随着温度的升高,环氟菌胺的水解速率加快;环氟菌胺在碱性条件下降解最快;十二烷基磺酸钠(sodium dodecyl sulfonate,SDS)抑制环氟菌胺的水解;腐植酸的浓度低于1 mg·L-1时促进环氟菌胺的水解,浓度高于1 mg·L-1时抑制环氟菌胺的水解;环氟菌胺在不同水体中的水解速率顺序为:海水>江水>河水,环氟菌胺在自然条件下的降解速率显著高于室内模拟条件。     

Light absorption by water-soluble organic carbon in atmospheric fine particles in the central Tibetan Plateau

Environmental Science and Pollution Research - Brown carbon (BrC) has recently received much attention because of its light absorption features. The chemical compositions, optical properties, and...     

基于GIS和贡献权重迭加方法的区域滑坡灾害易损性评价

区域滑坡易损性是指特定区域对滑坡灾害的破坏和损害的敏感性.根据易损性指标的科学性、可操作性以及可定量化等基本选取依据和研究区的区域特点,选择了人口密度、道路密度、建筑密度、林地密度、耕地密度、滑坡灾害密度6个指标.探讨了贡献率方法评价区域滑坡易损性的建模过程和数学表达.区域滑坡易损性定量表达为各指标的自权重与互权重以及指标的归一化值的乘积.以四川米易县为研究实例,对此评价方法进行了应用,在GIS系统中运用自然断点法进行了易损度区划和区划制图,结果显示,高易损度区、中易损度区、低易损度区分别占研究区域的7.13%、21.19%、71.68%,易损性分布基本上与人口密度、建筑密度和道路密度分布相一致,反应了基于贡献率的区域滑坡灾害易损性区划的合理性.     

全球近期灾害录（2009．10．11—12．10）

菲律宾遭热带风暴袭击 2009年10月11日,受热带风暴“凯萨娜”和“芭玛”袭击,菲律宾多个省份发生太面积洪灾和山体滑坡,两周来已造成超过600人死亡。     

全球近期灾害录(2009.8.11—10.10)

台湾一直升机执行灾区救援任务坠毁 2009年8月11日,台湾一架救援直升机在从屏东三地门出发前往雾台进行救灾任务时,不幸坠毁在屏东山区,已证实机上3名人员全部罹难. 巴布亚新几内亚一架包机失事 8月11日上午,一架载有13人的包机从巴新首都莫尔斯比港起飞,在前往巴新境内著名探险景点科科达山道的途中失踪,机上所有人员全部罹难.     

Calcite precipitation dominates the electrical signatures of zero valent iron columns under simulated field conditions

Calcium carbonate is a secondary mineral precipitate influencing zero valent iron (ZVI) barrier reactivity and hydraulic performance. We conducted column experiments to investigate electrical signatures resulting from concurrent CaCO₃ and iron oxides precipitation under simulated field geochemical conditions. We identified CaCO₃ as a major mineral phase throughout the columns, with magnetite present primarily close to the influent based on XRD analysis. Electrical measurements revealed decreases in conductivity and polarization of both columns, suggesting that electrically insulating CaCO₃ dominates the electrical response despite the presence of electrically conductive iron oxides. SEM/EDX imaging suggests that the electrical signal reflects the geometrical arrangement of the mineral phases. CaCO₃ forms insulating films on ZVI/magnetite surfaces, restricting charge transfer between the pore electrolyte and ZVI particles, as well as across interconnected ZVI particles. As surface reactivity also depends on the ability of the surface to engage in redox reactions via charge transfer, electrical measurements may provide a minimally invasive technology for monitoring reactivity loss due to CaCO₃ precipitation. Comparison between laboratory and field data shows consistent changes in electrical signatures due to iron corrosion and secondary mineral precipitation.     

Modeling the atmospheric transport and deposition of polychlorinated dibenzo-p-dioxins and dibenzofurans in North America

The atmospheric fate of polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) was simulated for the year 2000 in North America using a SMOKE/CMAQ-based chemical transport model that was modified for this purpose. The 1999 USEPA emission inventories of PCDD/Fs and criteria pollutants were used. The 1995 Canadian emission inventory of criteria pollutants and the 1995 Canadian area source emissions for PCDD/Fs were used with the 2000 Canadian point source emissions. Modifications to CMAQ involved coupling it with dual organic matter (OM) absorption and black carbon (BC) adsorption models to calculate PCDD/F gas–particle partitioning. The model satisfactorily reproduced the particle bound fractions at all rural sites for which there were measured data and across the whole domain, the modeled vs. measured differences in particle bound fractions were less than 20% for nearly all congeners. The model predicted ambient air PCDD/F concentrations were also consistent with measurements. Simulated deposition fluxes were within 58% of direct measurements. PCDD/F atmospheric depositions to each of the Great Lakes were estimated for the year 2000. The results indicate that approximately 76% of the total deposition of PCDD/Fs to the Great Lakes (in W-TEQ, or toxic equivalent units as defined by the World Health Organization) is attributed to PCDD/Fs absorbed into OM in aerosol. For all of the lakes, more than 92% of all deposition is particle phase wet deposition and only 5–8% is particle phase dry deposition. Wet deposition from the gas phase is negligible. Of the 17 toxic PCDD/F congeners, the Cl_4–5DD/F compounds contribute approximately 70% to the total atmospheric deposition to the Great Lakes. The seasonal changes in the PCDD/F deposition flux track variations in ambient temperature.