基于环境保护的机动车税优化建议

当前区域性大气污染问题突出,机动车使用造成的污染问题不可忽视。为解决区域性的大气污染问题,机动车税费的污染减排调控功能日益被政府和学者重视。研究围绕"如何使机动车税更好发挥环境保护的效果"的问题,比较了中日机动车税的结构和性质,分析了在购买、保有和使用等不同环节的机动车税的特点以及环保效果,并基于问卷调查分析中国私家车主不同环节机动车税的负担情况。研究表明,在机动车使用环节征收的成品油消费税污染调控效果要优于其他环节的税收;对商业用途的机动车使用征税仅有收入功能没有调控功能,建议将机动车相关税的作用重心从购买环节转移到使用环节上,并对商业用途和私人用途的机动车实施差别税率。     

浙江省火电行业主要污染物减排环境效益研究

利用美国环保局开发的新一代空气质量模式系统Models-3,对2010 年浙江省大气污染物进行数值模拟研究,并对SO₂、NO₂ 和PM₁₀ 等大气污染物浓度的模拟结果与监测结果进行了对比分析。结果表明,Models-3 系统能较好地反映浙江省的大气污染情况,模拟值与观测值的变化趋势具有较好的一致性,说明该模式能较好地进行大气污染物的分布特征和变化规律的研究。为定量分析电力行业多污染物协同控制与区域复合型大气污染之间的定量关系,评估不同控制情景下的环境质量效益,应用CMAQ 空气质量模型分别对2010 年基准排放情景和火电行业主要污染物(SO₂、NO_x 和烟尘)的三套减排控制情景,评价环境空气污染物SO₂、NO_x、PM_2.5 和PM₁₀ 状况进行模拟,评价污染物减排的环境效益。三套方案下PM_2.5 浓度下降比例分别为0.53%、0.55% 和0.57%,其中重点区域浓度下降比例分别为4.36%、4.38%和5.9%;PM₁₀ 浓度下降比例分别为0.40%、0.42% 和0.65%,重点区域下降比例分别为3.42%、5.82% 和8.16%;NO_x 浓度下降比例分别为12.4% 和13.3%,重点区域下降比例分别为13.8% 和16.9%;SO₂ 下降比例平均为11.24%,其中重点区域下降比例为14.4%。SO₂、NO_x 和烟(粉)尘协同减排对于浙江地区特别是重点区域的环境空气质量改善有着显著意义。     

云南曲靖地区铜的暴露与肺癌相关性研究

我国云南省曲靖的宣威和富源等地是全世界肺癌高发区,为了研究环境介质中铜(Cu)等重金属的暴露与体内分布特征,探讨Cu与肺癌的相关性,在当地开展肺癌环境流行病学调查,采集宣威和富源高发区人群饮食、饮水以及人体血浆和肺组织样品,微波消解ICP-MS法测定样品中Cu等元素.结果显示,当地居民使用燃料类型是影响肺癌高发的重要因素.高发区人群Cu的日摄入总量低于我国推荐的每日膳食中营养素供给量(RDA).肺癌组血液中Cu含量显著高于对照组,肺癌组织中Cu含量显著高于癌旁组织和正常组织,且肺癌患者的血浆和肺组织中Cu/Zn比值均升高.Pearson相关性分析结果表明,Cu和Ni、Cu和Pb呈显著正相关,提示在致癌作用上具有协同效应;Cu和Fe、Cu和Zn呈显著负相关,提示具有抑制或拮抗作用.多因素Logistic回归结果表明,Cu是肺癌发生的重要影响因素,人体中Cu含量和Cu/Zn比值可为肺癌的早期预防和诊断提供科学依据.     

汞在海洋浮游植物中的生物累积和毒性效应

浮游植物是海洋生态系统的主要初级生产者,同时作为食物也是许多水生生物摄取汞的主要途径。本文综述了近年来汞在海洋浮游植物中的最新研究进展,包括汞在浮游植物中的吸收、累积规律及其影响因素,汞对浮游植物的毒性效应(生长抑制、光合作用影响)以及生物的适应机制(汞的还原、螯合解毒、矿化固定等),最后对浮游植物中汞累积和毒性的未来研究方向进行了展望。     

Responses of bacterial strains isolated from drinking water environments to N-acyl-L-homoserine lactones and their analogs during biofilm formation

Often as a result ofbiofilm formation, drinking water distribution systems （DWDS） are regularly faced with the problem of microbial contamination. Quorum sensing （QS） systems play a marked role in the regulation of microbial biofilm formation; thus, inhibition of QS systems may provide a promising approach to biofilm formation control in DWDS. In the present study, 22 bacterial strains were isolated from drinking water-related environments. The following properties of the strains were investigated： bacterial biofilm formation capacity, QS signal molecule N-acyl-L-homoserine lactones （AHLs） production ability, and responses to AHLs and AHL analogs, 3-chloro-4-（dichloromethyl）-5-hydroxy-2（5H）- furanone （MX） and 2（5H）-furanone. Four AHLs were added to developed biofilms at dosages ranging from 0.1 nmol.L J to 100nmol.L1. As a result, the biofilm growth of more than 1/4 of the isolates, which included AHL producers and non-producers, were significantly promoted. Further, the biofilm biomasses were closely associated with respective AHLs concentrations. These results provided evidence to support the idea that AHLs play a definitive role in biofilm formation in many of the studied bacteria. Meanwhile, two AHLs analogs demon- strated unexpectedly minimal negative effects on biofilm formation. This suggested that, in order to find an applicable QS inhibition approach for biofilm control in DWDS, the testing and analysis of more analogs is needed.     

Comparative study on the efficiency and environmental impact of two methods of utilizing polyvinyl chloride waste based on life cycle assessments

Two processes of utilizing polyvinyl chloride （PVC） waste, an incineration process and a vacuum pyrolysis process, for energy conversion were compared to determine their efficiency and environmental perfor- mance. We carried out a life cycle assessment with each of the two processes to evaluate their environmental impact and defined the goals and limits of our remit. As well, we established an inventory of PVC waste from incineration and vacuum pyrolysis based on process analysis, data collection and calculations. The results show that electrical power output per unit mass of PVC waste in the incineration process was twice as high as that of the vacuum pyrolysis process. Incineration had a larger total environmental impact potential than vacuum pyrolysis. The total environmental impact potential of PVC waste from incineration was three times higher than that from vacuum pyrolysis. Incineration of PVC disposed 300 ng. 100 kgI of dioxins and vacuum pyrolysis 98.19 ng- 100 kgI of dioxins. As well, we analyzed the data for their uncertainty with results quantified in terms of three uncertainties： basic uncertainty, additional uncertainty, and computational uncertainty. The coefficients of variation of the data were less than 25% and the quality of the inventory data was acceptable with low uncertainty. Both PVC waste disposal processes were of similar quality and their results comparable. The results of our life cycle impact assessment （LCIA） showed considerable reliability of our methodology. Overall, the vacuum pyrolysis process has a number advantages and greater potential for development of PVC disposal than the incineration process.     

N2O emission from a sequencing batch reactor for biological N and P removal from wastewater

Nitrous oxide （N2O） is a greenhouse gas that can be released during biological nitrogen removal from wastewater. N2O emission from a sequencing batch reactor （SBR） for biological nitrogen and phosphorus removal from wastewater was investigated, and the aims were to examine which process, nitrification or denitrification, would contribute more to N2Oemission and to study the effects of heterotrophic activities on N2O emission during nitrification. The results showed that N2O emission was mainly attributed to nitrification rather than to denitrification. N2O emission during denitrification mainly occurred with stored organic carbon as the electron donor. During nitrification, NaO emission was increased with increasing initial ammonium or nitrite concentrations. The ratio of N2O emission to the removed ammonium nitrogen （N2O- N/NH4-N） was 2.5% in the SBR system with high heterotrophic activities, while this ratio was in the range from 0.14% to 1.06% in batch nitrification experiments with limited heterotrophic activities.     

A review of atmospheric mercury emissions,pollution and control in China

Mercury, as a global pollutant, has significant impacts on the environment and human health. The current state of atmospheric mercury emissions, pollution and control in China is comprehensively reviewed in this paper. With about 500-800 t of anthropogenic mercury emissions, China contributes 25%-40% to the global mercury emissions. The dominant mercury emission sources in China are coal combustion, non-ferrous metal smelting, cement production and iron and steel production. The mercury emissions from natural sources in China are equivalent to the anthropogenic mercury emissions. The atmospheric mercury concentration in China is about 2-10 times the background level of North Hemisphere. The mercury deposition fluxes in remote areas in China are usually in the range of 10-50μg·m^-2·yr^-1. To reduce mercury emissions, legislations have been enacted for power plants, non-ferrous metal smelters and waste incinerators. Currently mercury contented in the flue gas is mainly removed through existing air pollution control devices for sulfur dioxide, nitrogen oxides, and particles. Dedicated mercury control technologies are required in the future to further mitigate the mercury emissions in China.     

Enhanced organic phosphorus detection in sediments by foam separation and 31P-NMR

Phosphorus (P) is both a nutrient and a pollutant. For instance, excess P induces water eutrophication followed by death of fishes and other water life. Determination of organic P content in sediments is therefore important to study P cycling and environmental pollution. The most widely used method to determine organic P in sediments is NaOH–EDTA extraction followed by ³¹P-NMR detection. However, some organic P compounds are difficult to extract using NaOH–EDTA due to the low solubility, thus can not be detected by ³¹P NMR. Here, we used foam separation to determine organic P in sediment of North Canal of Tianjin City, China. Organic P was first enriched using foam separation coupled with NaOH extraction. The enriched organic P was then analyzed with ³¹P NMR. The results showed that, compared with the traditional extraction method, foam separation coupled with NaOH extraction enriched more P compound because ³¹P NMR detected an extra signal of teichoic acid at chemical shift 1.14. This teichoic acid signal was not detected in the extract prepared using only NaOH–EDTA. Our finding demonstrates that determination using foam separation followed by ³¹P NMR is feasible.     

口服纳米银对大鼠的生物有效性及其体内分布的研究

由于独特的抗菌特性,纳米银(AgNP)在诸多领域得到广泛应用,但是其生物有效性、动物组织分布及排出尚不清楚。将聚乙烯吡咯烷酮包被的AgNP溶液按照10 mg kg^-1给雌性SD大鼠灌胃,采用ICP-MS检测SD大鼠组织、粪便及尿液中总银浓度。实验结果表明,AgNP通过小肠吸收后,可以通过血液循环快速分布在肝、肾、脾、肺、脑等靶器官。灌胃后1 h,大鼠各组织中总银浓度达到最大值(肝、肾、脾、肺、脑中银浓度分别为0.29 ± 0.13 mg kg^-1、0.23 ± 0.04 mg kg^-1、0.17 ± 0.05 mg kg^-1、0.11 ± 0.01 mg kg^-1、0.06 ±0.02 mg kg^-1),之后银浓度随时间降低直至和对照组无显著性差异。在灌胃途径下,AgNP对SD大鼠的有效性为8.5%,且73%的AgNP是通过粪便的途径排出体外。