珠海2019年秋季一次大气污染过程的特征、 成因及来源分析

2019年秋季在珠三角典型沿海城市珠海观测到一次中重度污染过程,本文对此次过程的污染特征、形成机制和来源进行了研究.通过 采集PM_2.5样品,分析了9种水溶性无机离子（WSIIs）、有机碳（OC）、元素碳（EC）和水溶性有机碳（WSOC）等化学组分的浓度水平和污染特征;进一步结合污染过程中的不利天气形势、72 h后向气流轨迹及PM_2.5的潜在源贡献因子（WPSCF）和浓度权重轨迹（WCWT）等方法分析了污染的形成机制和来源.结果表明,有机物（OM）是污染时期PM_2.5中增长最快的组分,其次是占WSIIs约82.46%的SO₄^2-、NO₃^-和NH₄⁺（SNA）. NO₃^-/SO₄^2-均值为0.20,表明珠海以固定源污染为主;硫氧化率（SOR）均值为0.65,氮氧化率（NOR）均值为0.08,高温高湿的气象条件可能是 造成珠海比中国其他城市SOR偏高而NOR偏低的原因.在污染时段,二次有机碳（SOC）明显增加,WSOC/SOC随污染物的升高而降低并趋近于1,因此, 污染时期的WSOC可能主要是二次生成的.副高控制型、台风外围型和高压出海型等天气形势控制着整个珠三角地区时,不利于污染物的传输和扩散,使污染加剧.后向气流轨迹分析表明,污染时期的气团轨迹主要来自于高污染的内陆地区,这可能是造成此次污染形成的重要原因和来源.WPSCF和WCWT的高值区主要集中在江西、广东等内陆地区,因此,珠海在控制本地排放的同时,也应该关注上风向临近省市的污染排放.     

我国区域空气污染治理效率及其影响机制——基于超效率SBM模型和门槛回归模型

随着人民对美好生活需求的日益增长,政府空气污染治理的效率问题日益得到重视。本文从地方政府空气污染治理效率及其影响因素的视角入手,以全国30个省份为研究对象,运用超效率SBM模型测算2003—2015年各省级区域的空气污染治理效率。在此基础上,运用门槛回归模型分析政府空气污染治理效率的影响机制。研究表明:①地区间空气污染治理效率差异性较为显著。中部、西部空气污染治理效率整体呈下降趋势。东部和东北地区空气污染治理效率则上升比较平稳。②政策规划、碳源、污染物排放和环境治理投入表现出双重门槛特征,其中碳源对空气污染治理效率影响显著,而以碳为首的能源消费结构则主要对中部和西部空气污染治理效率产生影响。落后地区政府应注重产业升级,财政上应对碳税等税目进行征收,产业上应鼓励企业创新,并对落后企业进行倒逼升级。     

Mitigating Impact of Devils Lake Flooding on the Sheyenne River Sulfate Concentration

Devils Lake is a terminal lake located in northeast North Dakota. Because of its glacial origin and accumulated salts from evaporation, the lake has a high concentration of sulfate compared to the surrounding water bodies. From 1993 to 2011, Devils Lake water levels rose by ~10 m, which flooded surrounding communities and increased the chance of an overspill to the Sheyenne River. To control the flooding, the State of North Dakota constructed two outlets to pump the lake water to the river. However, the pumped water has raised concerns about of water quality degradation and potential flooding risk of the Sheyenne River. To investigate these perceived impacts, a Soil and Water Assessment Tool (SWAT) model was developed for the Sheyenne River and it was linked to a coupled SWAT and CE‐QUAL‐W2 model that was developed for Devils Lake in a previous study. While the current outlet schedule has attempted to maintain the total river discharge within the confines of a two‐year flood (36 m³/s), our simulation from 2012 to 2018 revealed that the diversion increased the Sheyenne River sulfate concentration from an average of 125 to >750 mg/L. Furthermore, a conceptual optimization model was developed with a goal of better preserving the water quality of the Sheyenne River while effectively mitigating the flooding of Devils Lake. The optimal solution provides a “win–win” outlet management that maintains the efficiency of the outlets while reducing the Sheyenne River sulfate concentration to ≤600 mg/L.     

Inverse uncertainty characteristics of pollution source identification for river chemical spill incidents by stochastic analysis

Identifying source information after river chemical spill occurrences is critical for emergency responses. However, the inverse uncertainty characteristics of this kind of pollution source inversion problem have not yet been clearly elucidated. To fill this gap, stochastic analysis approaches, including a regional sensitivity analysis method, identifiability plot and perturbation methods, were employed to conduct an empirical investigation on generic inverse uncertainty characteristics under a well-accepted uncertainty analysis framework. Case studies based on field tracer experiments and synthetic numerical tracer experiments revealed several new rules. For example, the release load can be most easily inverted, and the source location is responsible for the largest uncertainty among the source parameters. The diffusion and convection processes are more sensitive than the dilution and pollutant attenuation processes to the optimization of objective functions in terms of structural uncertainty. The differences among the different objective functions are smaller for instantaneous release than for continuous release cases. Small monitoring errors affect the inversion results only slightly, which can be ignored in practice. Interestingly, the estimated values of the release location and time negatively deviate from the real values, and the extent is positively correlated with the relative size of the mixing zone to the objective river reach. These new findings improve decision making in emergency responses to sudden water pollution and guide the monitoring network design.

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基于着生硅藻指数的梧桐河水生态健康评价

在黑龙江省梧桐河,调查了13个点位的着生硅藻群落结构和水环境特征,应用8种硅藻指数对该河流水生生态系统进行健康评价,并在此基础上应用主成分分析、相关分析、冗余分析、箱型图分析等统计分析方法研究了影响梧桐河着生藻类群落的主要环境因子和8种硅藻指数在梧桐河的适用情况。结果显示:梧桐河存在一定程度的环境污染,优势种以小型异极藻(Gomphonema parvulum)等耐污种为主。8个硅藻指数中,硅藻属指数(Generic Index of Diatom,GI)、澳大利亚河流硅藻生物评价指数(Diatom Index for Australian Rivers,DIAR;Diatom Species Index for Bioassessment of Australian Rivers,DSIAR)评价结果偏差较大,在梧桐河不适用;相似度指数(Jaccard Index,JI)与富营养化硅藻指数(Trophic Diatom Index,TDI)评价结果较为严格,评分明显偏低;硅藻污染耐受指数(Pollution Tolerance Index,PTI)、硅藻生物评价指数(Diatom Bioassessment Index,DBI)和生物硅藻指数(Biological Diatom Index,BDI)在梧桐河流域适用性最好。根据冗余分析(RDA),将梧桐河流域点位分为3组,第一组点位为中-重度污染,主要影响因子为流速和总磷;第二组点位为轻-中度污染,主要影响因子为磷酸盐、氨氮和溶解氧;第三组点位为轻污染-清洁,主要影响因子为p H和电导率。     

应用鱼类生物完整性指数评价荔浦河河流健康

生物完整性指数是河流生态系统健康评价主要方法之一。为评价荔浦河河流健康状况,选择鱼类作为指示生物,构建了基于鱼类生物完整性指标体系。2017年1月、4月、7月和10月对荔浦河4次采样共采集到鱼类21 192尾,经鉴定共计94种,隶属于6目17科62属。以S1(修仁镇)、S10(马岭镇)、S11(双江镇)作为参考点,经过分布范围分析、箱体图判别能力分析及相关性分析等指标筛选过程从25个候选指标筛选出5个指标,即鱼类总物种数、Shannon-Wiener多样性指数、肉食性鱼类数量百分比、敏感性鱼类数量百分比、产漂浮型卵鱼类数量百分比。将荔浦河河流健康等级分为"健康"、"一般"、"较差"、"极差"和"无鱼"5个等级。结果表明,荔浦河青山镇、荔浦县及蒲芦乡河段健康状态为"一般"水平,东昌镇、龙怀乡、杜莫镇及新坪镇河段健康状态为"较差"水平,茶城乡河段健康状态为"极差"水平。筑坝工程、架桥工程和修路工程等人类活动导致荔浦河支流上的健康状况比干流更差。上述研究结果可为荔浦河的河流管理和保护提供理论依据和技术支持。     

Monitoring air quality with lichens: a comparison between mapping in forest sites and in open areas

Four different methods of epiphytic lichen mapping were used for the assessment of air quality in the region under the influence of the Sostanj Thermal Power Plant (Salek Valley, Slovenia). Three methods were based on the presence of different lichen species (VDI, EU and ICP-Forest), the fourth on a frequency and coverage assessment of different growth forms of epiphytic lichens, e.g. crustose, foliose and fruticose (SI). A comparison of the results from the assessment of air quality between forest sites (ICP-Forest, SI) and open areas (VDI, EU and SI), obtained by the different methods of epiphytic lichen mapping, is presented in the contribution. Data showed that lichen species richness is worse in forest sites in comparison with open areas. From the data obtained it can be concluded that epiphytic lichen mapping in open areas is a better method for the assessment of air pollution in a given area than mapping in forest sites. The species-based methods in open areas are more powerful and useful for air quality assessment in polluted research areas than the SI and ICP-Forest methods.     

Heavy metal contamination in the vicinity of an industrial area near Bucharest

BACKGROUND, AIMS AND SCOPE: Chromium enters into the aquatic environment as a result of effluent discharge from steel works, electroplating, leather tanning industries and chemical industries. As the Cr(VI) is very harmful to living organisms, it should be quickly removed from the environment when it happens to be contaminated. Therefore, the aim of this laboratory research was to develop a rapid, simple and adaptable solvent extraction system to quantitatively remove Cr(VI) from polluted waters. METHODS: Aqueous salt-solutions containing Cr(VI) as CrO4(2-) at ppm level (4-6 ppm) were prepared. Equal volumes (5 ml) of aqueous and organic (2-PrOH) phases were mixed in a 10 ml centrifuge tube for 15 min, centrifuged and separated. Concentrations of Cr(VI), in both the aqueous and organic phases, were determined by atomic absorption spectrometry. The effects of salt and acid concentrations, and phase-contact time on the extraction of Cr(VI) were investigated. In addition, the extraction of Cr(VI) was assessed in the presence of tetramethylammonium chloride (TMAC) in 2-PrOH phase. Effects of some other metals, (Cd(II), Co(II), Cu(II), Ni(II) and Zn(II)), on the extraction of Cr(VI) were also investigated. RESULTS AND DISCUSSION: The Cr(VI) at ppm level was extracted quantitatively by salting-out the homogeneous system of water and 2-propanol(2-PrOH) using chloride salts, namely CaCl2 or NaCl, under acidic chloride media. The extracted chemical species of Cr(VI) was confirmed to be the CrO3Cl-. The ion-pair complex extracted into the organic phase was rationalized as the solvated ion-pair complex of [2-PrOH2+, CrO3Cl-]. The complex was no longer stable. It implied the reaction between extracted species. Studies revealed that salts and acid directly participated in the formation of the above complex. Use of extracting agents (TMAC) didn't show any significant effect on the extraction of Cr(VI) under high salting-out conditions. There is no significant interference effect on the extraction of Cr(VI) by the presence of other metals. The Cr(VI) in the organic phase was back-extracted using an aqueous ammonia solution (1.6 mol dm(-3)) containing 3 mol dm(-3) NaCl. The extraction mechanism of Cr(VI) is also discussed. CONCLUSIONS: Salting-out of homogeneous mixed solvent of 2-propanol can be employed to extract Cr(VI) quantitatively, as an ion-pair of [2-PrOH2+ * CrO3Cl-] solvated by 2-PrOH molecules. Then, the complex becomes 'solvent-like' and is readily separated into the organic phase. The increase of Cl- ion concentration in the aqueous phase favors the extraction. The 2-PrOH, salts and acid play important roles in the extraction process. There is no need to use an extracting agent at a high salting-out condition. RECOMMENDATIONS AND PERSPECTIVES: Chromium(VI) must be quickly removed before it enters into the natural cycle. As the 2-PrOH is water-miscible in any proportion, ion-pairing between 2-PrOH2+ and CrO3Cl- becomes very fast. As a result, Cr(VI) can easily be extracted. Therefore, the method is recommended as a simple, rapid and adaptable method to quickly separate Cr(VI) from aqueous samples.     

区域规划环境影响跟踪评价的理论研究

随着环境影响评价制度的深入实施,其实施领域已由项目环评向区域环评和规划环评转变,评价内容也由广泛实施的预测评价向后评价和跟踪评价转变。然而,对于区域规划环评的评价层次、评价程序和评价内容,目前还没有明晰的认识;同时,对于促进规划环评有效实施的跟踪评价,其相关的理论和实践研究几乎没有。文中就此问题作了深入探讨。     

Levels of perfluorochemicals in water samples from Catalonia,Spain: is drinking water a significant contribution to human exposure?

Background, aim, and scope  In recent years, due to a high persistence, biomagnification in food webs, presence in remote regions, and potential toxicity, perfluorochemicals (PFCs) have generated a considerable interest. The present study was aimed to determine the levels of perfluorooctane sulfonate (PFOS), perfluorooctanoic acid (PFOA), and other PFCs in drinking water (tap and bottled) and river water samples from Tarragona Province (Catalonia, Spain). Materials and methods  Municipal drinking (tap) water samples were collected from the four most populated towns in the Tarragona Province, whereas samples of bottled waters were purchased from supermarkets. River water samples were collected from the Ebro (two samples), Cortiella, and Francolí Rivers. After pretreatment, PFC analyses were performed by HPLC-MS. Quantification was done using the internal standard method, with recoveries between 68% and 118%. Results  In tap water, PFOS and PFOA levels ranged between 0.39 and 0.87 ng/L (0.78 and 1.74 pmol/L) and between 0.32 and 6.28 ng/L (0.77 and 15.2 pmol/L), respectively. PFHpA, PFHxS, and PFNA were also other detected PFCs. PFC levels were notably lower in bottled water, where PFOS could not be detected in any sample. Moreover, PFHpA, PFHxS, PFOA, PFNA, PFOS, PFOSA, and PFDA could be detected in the river water samples. PFOS and PFOA concentrations were between <0.24 and 5.88 ng/L (<0.48 and 11.8 pmol/L) and between <0.22 and 24.9 ng/L (<0.53 and 60.1 pmol/L), respectively. Discussion  Assuming a human water consumption of 2 L per day, the daily intake of PFOS and PFOA by the population of the area under evaluation was calculated (0.78–1.74 and 12.6 ng, respectively). It was found that drinking water might be a source of exposure to PFCs as important as the dietary intake of these pollutants. Conclusions  The contribution of drinking water (tap and bottled) to the human daily intake of various PFCs has been compared for the first time with data from dietary intake of these PFCs. It was noted that in certain cases, drinking water can be a source of exposure to PFCs as important as the dietary intake of these pollutants although the current concentrations were similar or lower than those reported in the literature for surface water samples from a number of regions and countries. Recommendations and perspectives  Further studies should be carried out in order to increase the knowledge of the role of drinking water in human exposure to PFCs.