污泥中潜在的二■■污染物质

依据国内外最近的检测结果对污泥中二■■类物质的研究进行论述,探讨其来源、组成分布、环境行为及潜在危害。研究表明,焚烧过程排放?成了环境中二■■的本底来源,除此之外的二■■主要来源于废水处理(包括生活污水与工业污水)形成的污泥,并且污泥中二■■的含量较高。鉴于二■■的毒理特性、以往的二■■污染事件及我国对污泥的处理方式,急需查明堆肥与填埋处理的污泥中的二■■现状,并以此为依据制定二■■毒物的排放标准及其在环境中的限额。      

北江底泥中重金属污染特征及生态危害评价

测定了北江五个监测断面的底泥中重金属镉、铬、铜、铅、锌的含量,镉含量在11.7-76.0mg/ks之间,铬含量在46.5-112.3mg/kg之间,铜含量在62.0～173.7mg/kg之间,铅含量在148.7-491.0mg/kg之间,锌含量在303.3-1453.0mg/kg之间,这五种重金属含量均超出广东省土壤背景值和我国湖泊底泥中重金属的平均值.经计算,北江底泥中这五种重金属具有较强的相关性(相关系数在0.89～0.99之间),表明其具有同源性.采用瑞典学者Hakanson提出的潜在生态危害指数法对北江五个底泥监测断面的镉、铬、铜、铅、锌进行了潜在生态危害评价,其潜在生态危害指数均大于600,表明北江五个底泥采样断面的重金属潜在生态危害均为很强.     

黄土高原蒸发力的计算和应用——兼谈改善生态环境的途径

蒸发力是气候学上的一个重要特征量。在水利工程设计、灌溉定额的制定、农林牧的合理布局需要以蒸发力资料为依据。彭曼公式具有较可靠的物理基础和计算精度较高的优点,在国际上得到了广泛的应用。我国某些学者在运用该公式时,未考虑海拔高度对蒸发力的影响,因此在高海拔地区应用彭曼公式会产生较大的误差。 本文应用高度订正后的彭曼公式:计算了黄土高原地区的蒸发力。 森林减弱了近地层风速,降低了该地区的蒸发力,农田水分状况得到了改善。     

浅论人为灾害

本文着重对人为灾害进行了讨论，指出了人为灾害的主要特征，即它超越了时间和空间的界限，具有不确定性和惩罚性，并由此将人为灾害划分为随机、次生、潜在三个系统．在以翔实的资料描述人为灾害现状后，提出了防治对策．     

Environmental impact and health risk assessment of volatile organic compound emissions during different seasons in Beijing

Volatile organic compounds (VOCs) are major contributors to air pollution. Based on the emission characteristics of 99 VOCs that daily measured at 10 am in winter from 15 December 2015 to 17 January 2016 and in summer from 21 July to 25 August 2016 in Beijing, the environmental impact and health risk of VOC were assessed. In the winter polluted days, the secondary organic aerosol formation potential (SOAP) of VOC (199.70 ± 15.05 μg/m³) was significantly higher than that on other days. And aromatics were the primary contributor (98.03%) to the SOAP during the observation period. Additionally, the result of the ozone formation potential (OFP) showed that ethylene contributed the most to OFP in winter (26.00% and 27.64% on the normal and polluted days). In summer, however, acetaldehyde was the primary contributor to OFP (22.00% and 21.61% on the normal and polluted days). Simultaneously, study showed that hazard ratios and lifetime cancer risk values of acrolein, chloroform, benzene, 1,2-dichloroethane, acetaldehyde and 1,3-butadiene exceeded the thresholds established by USEPA, thereby presenting a health risk to the residents. Besides, the ratio of toluene-to-benzene indicated that vehicle exhausts were the main source of VOC pollution in Beijing. The ratio of m-/p-xylene-to-ethylbenzene demonstrated that there were more prominent atmospheric photochemical reactions in summer than that in winter. Finally, according to the potential source contribution function (PSCF) results, compared with local pollution sources, the spread of pollution from long-distance VOCs had a greater impact on Beijing.     

Spatial distribution and source identification of wet deposition at remote EANET sites in Japan

Wet deposition of major ions was discussed from the viewpoint of its potential sources for six remote EANET sites in Japan (Rishiri, Happo, Oki, Ogasawara, Yusuhara, and Hedo) having sufficiently high data completeness during 2000–2004. The annual deposition for each site ranged from 12.1 to 46.6 meq m⁻² yr⁻¹ for nss-SO₄²⁻, from 5.0 to 21.9 meq m⁻² yr⁻¹ for NO₃⁻. The ranges of annual deposition of the two ions for the sites were lower than those for urban and rural sites in Japanese Acid Deposition Survey by Ministry of the Environment, Japan, and higher than those for global remote marine sites. Factor analysis was performed on log-transformed daily wet deposition of major ions for each site. The obtained two factors were interpreted as (1) acid and soil source (or acid source for some sites), and (2) sea-salt source for all the sites. This indicates that wet deposition of ions over the remote areas in Japan has a similar structure in terms of types of sources. Factor scores of acid and soil source were relatively high during Kosa (Asian dust) events in spring in western Japan. Back-trajectories for high-deposition episodes of acid and soil source (or acid source) for the remote sites showed that episodic air masses frequently came from the northeastern area of Asian Continent in spring and winter, and from central China in summer and autumn. This indicates a large contribution of continental emissions to wet deposition of ions over the remote areas in Japan.     

Aktuelle und künftige Emissionen treibhauswirksamer fluorierter Verbindungen in Deutschland

Zusammenfassung  Die fluorierten Verbindungen Schwefelhexafluorid (SF₆), perfluorierte Fluorkohlenwasserstoffe (CF₄, C₂F₆) und wasserstoffhaltige Fluorkohlenwasserstoffe (H-FKW) z?hlen zu den atmosph?rischen Spurengasen mit extrem hohen Treibhauspotentialen. Untersucht werden für Deutschland ihre realen Emissionen für 1990–1995, und Prognosen für die Jahre bis 2020 werden aufgestellt. Diesen Prognosen zufolge vermindern sich die j?hrlichen Freisetzungen von CF₄/C₂F₆ von 1990 bis 2000 von 335 t/34 t auf 100 t/10 t infolge Automatisierungsma?nahmen an der Hauptquelle (Aluminiumhütten). Die Emissionen von SF₆ bleiben dagegen bis 2020 im Schwankungsbereich zwischen 200 und 300 t j?hrlich. Hauptemittenten sind nicht elektrische Schaltanlagen, da diese relativ dicht sind und über ein Entsorgungs-und Wiederaufarbeitungskonzept für gebrauchtes Gas verfügen, sondern mit gro?em Abstand Autoreifen und Schallschutzscheiben. Bei den erst seit 1990 gezielt als FCKW-Nachfolger eingesetzten H-FKW ist mit fortschreitender FCKW-Substitution in der station?ren und mobilen K?lte-und Klimatechnik, bei PU-Montageschaum und Asthmasprays mit einer sprunghaften Zunahme der Emissionen bis auf über 9700 t/a ab dem Jahr 2007 zu rechnen, sofern sich nicht halogenfreie Alternativen st?rker durchsetzen. Im Jahr 2020 werden bei Annahme dieser Trends die kumulierten Emissionen der genannten fluorierten Verbindungen der Treibhauswirkung von 25 Mio. t CO₂ entsprechen (GWP-Betrachtungszeitraum: 100 Jahre).      

沈阳市能源需求预测及潜力分析

本文采用逐步回归分析法预测能源需求，结果表明能源消费量与国民生产总值显著相关，预测到２０００年，沈阳市短缺能源达２００万吨标煤．为此，文中进一步提出了提高能源开发、利用潜力的途径和措施及其环境效益．     

Distinct potential aerosol masses under different scenarios of transport at a suburban site of Beijing

In order to evaluate the secondary aerosol formation potential at a suburban site of Beijing,in situ perturbation experiments in a potential aerosol mass(PAM) reactor were carried out in the winter of 2014.The variations of secondary aerosol formation as a function of time,OH exposure,and the concentrations of gas phase pollutants and particles were reported in this study.Two periods with distinct secondary aerosol formation potentials,marked as Period Ⅰ and Period Ⅱ,were identified during the observation.In Period Ⅰ,the secondary aerosol formation potential was high,and correlated well to the air pollutants,i.e.,SO_2,NO_2,and CO.The maximal secondary aerosol formation was observed with an aging time equivalent to about 3 days of atmospheric oxidation.In period Ⅱ,the secondary aerosol formation potential was low,with no obvious correlation with the air pollutants.Meanwhile,the aerosol mass decreased,instead of showing a peak,with increasing aging time.Backward trajectory analysis during the two periods confirmed that the air mass in Period Ⅰwas mainly from local sources,while it was attributed mostly to long distance transport in Period Ⅱ.The air lost its reactivity during the long transport and the particles became highly aged,resulting in a low secondary aerosol formation potential.Our experimental results indicated that the in situ measurement of the secondary aerosol formation potential could provide important information for evaluating the contributions of local emission and long distance transport to the aerosol pollution.     

Distribution and assessment of heavy metals in the surface sediment of Yellow River, China

Large amounts of heavy metals discharged by industrial cities that are located along the middle reach of Yellow River, China have detrimental impacts on both the ecological environment and human health. In this study, fourteen surface sediment samples were taken in the middle reach of the Yellow River. Contents of Zn, Pb, Ni, Cu, Cr, Cd, As were measured, and the pollution status was assessed using three widely used pollution assessment methods, including the single factor index method, Nemerow pollution index method and potential ecological risk index. The concentrations of the studied heavy metals followed the order: Zn > Cr > Cu > Ni > Pb > As > Cd. Nearly 50% of sites had Cu and Cr accumulation. The concentration of Cu at the Yiluo River exceeded the secondary standard value of the Environmental quality standard for soils. Comparison of heavy metal concentrations between this study and other selected rivers indicated that Cu and Cr may be the major pollutants in our case. The single factor index indicated that many samples were at high levels of pollution for Cu and Cd; the Nemerow pollution index indicated that the Yihe River, Luohe River, Yiluo River and Huayuankou were polluted. According to the results of potential ecological risk assessment, Cd in the tributaries of Luo River, Yihe River, and Yiluo River showed high risk toward the ecosystem and human health, Cd in Huanyuankou and Cu in Yiluo River showed a middle level of risk and other samples were at a low level of risk.