燃煤电厂大气污染物排放考核时间间隔的建议

新的《火电厂大气污染物排放标准》和新《环境保护法》实施后，燃煤火电企业的依法治企自觉性不断提高，但由于不同的环保管理文件对超标处罚依据和处罚手段不同，造成政府对企业处罚的自由裁量权加大，对企业造成一定的压力与困惑。结合企业实际运行情况对燃煤电厂大气污染物排放考核时间间隔提出建议。     

郑州市土壤与绿色植物中汞的分布特征

汞污染具有生物积累性,因而得到社会广泛关注。研究监测和评估了郑州市城区土壤和绿色植物叶片中汞浓度、分布、污染水平等。研究发现郑州市主城区土壤总汞浓度为0. 150～0. 958 mg/kg,平均浓度为0. 448 mg/kg;郑州市主城区绿色植物叶片总汞浓度为0. 017～0. 249 mg/kg,平均浓度为0. 107 mg/kg;土壤和叶片中汞浓度按功能区排序为交通枢纽区工业区商业区行政区高教区住宅区。采用地累积指数法对郑州市80个土壤样品的汞污染水平进行评估,结果显示60%受到轻度污染,35%受到偏中度污染,5%受到中度污染。研究较为全面地分析了土壤汞污染的现状及浓度,为郑州市土壤汞污染防治提供参考。     

A new approach to Assess Atmospheric Nitrogen Deposition by Way of Standardized Exposition of mosses

A standardized method of moss exposition for assessing variations in nitrogen deposition was tested in the western part of Germany. Six pleurocarpous moss species were transplanted to two sites differing in their deposition rates but being comparable as to their climatic conditions. The mosses were exposed in standardized containers over a period of 12 months; the focus of interest was the effect of N deposition on nitrogen content and on ¹⁵N natural abundance (δ¹⁵N-values). Within the first nine months only trends could be observed. However, after one year all species tested showed significantly higher N concentrations at the highly polluted site. Besides, more negative δ¹⁵N-values possibly reflecting the higher ammonium input were detected at this site. Surprisingly, most of the plants though being kept in plastic containers without a favourable substratum did not show any conspicuous deficiency symptoms. The potential advantages of a standardized moss exposition for N monitoring purposes are discussed. It is concluded that the method presented here can yield significant results in particular if the number of testing sites is increased.     

Seasonal and Inter-Annual Variations in Methyl Mercury Concentrations in Zooplankton from Boreal Lakes Impacted by Deforestation or Natural Forest Fires

We compared the effects of natural and anthropogenic watershed disturbances on methyl mercury (MeHg) concentration in bulk zooplankton from boreal Shield lakes. MeHg in zooplankton was monitored for three years in nine lakes impacted by deforestation, in nine lakes impacted by wildfire, and in twenty lakes with undisturbed catchments. Lakes were sampled during spring, mid- and late summer. MeHg in zooplankton showed a seasonal trend: concentrations were the lowest in spring, then peaked in mid-summer and decreased in late summer. Over the three study years, MeHg concentrations observed in mid-summer in zooplankton from forest harvested lakes were significantly higher than in reference and fire-impacted lakes, whereas differences between these two groups of lakes were not significant. The pattern of distribution of MeHg in zooplankton during the different seasons paralleled that of dissolved organic carbon (DOC), which is known as a vector of Hg from watershed soils to lake water. Besides DOC, MeHg in zooplankton also showed a positive significant correlation with epilimnetic temperature and sulfate concentrations. An inter-annual decreasing trend in MeHg was observed in zooplankton from reference and fire-impacted lakes. In forest harvested lakes, however, MeHg concentrations remained higher and nearly constant over three years following the impact. Overall these results indicate that the MeHg pulse observed in zooplankton following deforestation by harvesting is relatively long-lived, and may have repercussions to the accumulation of MeHg along the food chain. Therefore, potential effects of deforestation on the Hg contamination of fish should be taken into account in forest management practices.     

Acid Deposition in the Tuscan Appennines During the Dry Period 1988-89

The typical parameters of acid precipitation are evaluated in the forest of Vallombrosa (Tuscan Appennines) during the dry period 1988-89. Individual rain events (dry and wet deposition) were sampled in a clearing of the forest and below the canopy of an evergreen tree as well as a deciduous broadleaf tree.

In atmospheric precipitation the pH values usually vary around 4.4, with neutralization in the hot season due to calcareous material from distant sources. Relatively large concentrations of Pb and Cd are found in rain, but only in a small amount in canopy leachate. Aluminium, manganese and iron are more significantly washed off than Pb and Cd.     

盐酸溶液改性蛭石对气态单质汞的吸附性能

采用盐酸溶液对蛭石进行浸渍处理，考察了盐酸溶液改性蛭石对气态单质汞的吸附能力。研究结果表明：盐酸溶液改性蛭石对气态单质汞的吸附效果好于未改性蛭石，盐酸浓度为4．0mol／L时，盐酸溶液改性蛭石对气态单质汞的吸附效果较佳；进气中气态单质汞的质量浓度越高，盐酸溶液改性蛭石对气态单质汞的去除率越低；适当提高吸附温度对盐酸溶液改性蛭石吸附气态单质汞较有利；降低蛭石粒径，盐酸溶液改性蛭石对气态单质汞的去除率提高。     

典型西南工业城市柳州市核心区大气污染物时空分布与气象因素研究

为研究柳州市核心区大气污染物浓度时空变化规律与气象因素之间的关系,统计分析了2018年全年研究区内6个自动监测站点PM_(2.5)、PM_(10)、SO_2、NO_2、O_3和CO的浓度监测数据和气象站气象数据,并对28次超标日污染物来源进行了解析.结果显示:①核心区颗粒污染物污染较为严重,且以PM_(2.5)为主的细颗粒污染物仍为柳州市主要的大气污染物;各污染物月均浓度季节差异显著,除NO_2外柳州大气污染物浓度下降明显,指示柳州市多项节能减排综合整治措施成效显著;PM_(2.5)、PM_(10)、CO受早晚高峰期影响,浓度日变化均呈双峰型;NO_2在不同季节峰型不同,作为O_3前体物其浓度日变化与O_3相反,呈现"早峰午谷"的变化趋势.②通过对污染物浓度插值发现,由于核心区主要工商业区位于西部且处于主导风向下风向,故PM_(2.5)和SO_2浓度西北高、东南低,PM_(10)、NO_2和CO浓度西南高、东北低;核心区东部的山区为O_3生成带来大量前体物,使O_3浓度东南高、西北低.③由于气候特征,核心区春、夏季主要气象因素均为降水量;秋季的主要气象因素是风速,风速与污染物的负相关关系表明了风的扩散效应;冬季大部分污染物与气象因素的相关性不显著,表明人为因素对污染物的影响大于气象因素;核心区大气污染物主要来源于局地排放和区域传输,且南北主导风向对大气污染影响最大.④HYSPLIT模型结果指示柳州超标日大气污染物主要来自于珠三角地区,且陆源颗粒物浓度普遍比海洋源高,来自南部的远距离输送气流颗粒物含量最低,表明远距离输送为影响颗粒物传播的主要原因.     

基于卫星遥感气溶胶产品评估体系的气溶胶时空分布及变化趋势表征

卫星遥感气溶胶虽然空间覆盖度高,但不同产品数据在准确性和适用性上存在显著差异.为了能够科学定量的衡量各个产品的优劣,选择最合适的气溶胶产品,该研究以数学统计为基础,提出了一种卫星遥感气溶胶产品评估体系,并依此确定了全球6个人口密集地区的最优卫星数据集,在此基础上开展了近10年的（2009—2018）气溶胶时空变化分析.结果表明暗像元算法在植被覆盖度高的地区表现最好,深蓝算法在亮地表的沙漠干旱地区更占优势,而暗像元-深蓝融合算法在土地类型复杂且气溶胶来源多变时得以突出.人口密集的6个区域中,除了区域A和区域B,其它地区的大气污染水平整体偏高.其中,A、B、E的气溶胶负荷呈下降变化,区域F基本不变,其余区域上升变化.评估体系的建立为气溶胶遥感产品的选取提供了新的衡量方法,且该文关于气溶胶时空分布及变化的分析可以为区域性气溶胶研究提供一定的参考价值.     

中国菌糠露天焚烧污染物排放时空分布特征

基于我国2000~2017年食用菌年产量数据,采用排放因子法估算了菌糠露天焚烧的污染物排放量,利用Mann-Kendall法和聚类分析法分析了排放量的时空分布特征,使用回归分析法预测了污染物的排放趋势.结果表明：（1）2000~2017年全国菌糠露天焚烧污染物排放量持续上升,PM_2.5、CO₂、CO、CH₄、NMVOCs、PAHs、NO_x、SO₂累积排放量分别为1.40×10⁶,3.48×10⁸,1.99×10⁷,8.43×10⁵,2.08×10⁶,3.00×10⁴,6.34×10⁵,8.29×10⁴t;（2）污染物排放量较高的省区包括山东、黑龙江、浙江、湖南、江苏、福建和河南,排放量较低的省区包括贵州、宁夏、天津、北京、新疆、重庆、甘肃;（3）预计2021年菌糠焚烧污染物总排放量高达4.25×10⁷t,其对生物质焚烧污染物总排放量的贡献率约为19.82%.我国菌糠露天焚烧污染物排放规模较大,应予以重点关注.     

Reactive uptake of NO2 on volcanic particles: A possible source of HONO in the atmosphere

The heterogeneous degradation of nitrogen dioxide (NO₂) on five samples of natural Icelandic volcanic particles has been investigated. Laboratory experiments were carried out under simulated atmospheric conditions using a coated wall flow tube (CWFT). The CWFT reactor was coupled to a blue light nitrogen oxides analyzer (NO_x analyzer), and a long path absorption photometer (LOPAP) to monitor in real time the concentrations of NO₂, NO and HONO, respectively. Under dark and ambient relative humidity conditions, the steady state uptake coefficients of NO₂ varied significantly between the volcanic samples probably due to differences in magma composition and morphological variation related with the density of surface OH groups. The irradiation of the surface with simulated sunlight enhanced the uptake coefficients by a factor of three indicating that photo-induced processes on the surface of the dust occur. Furthermore, the product yields of NO and HONO were determined under both dark and simulated sunlight conditions. The relative humidity was found to influence the distribution of gaseous products, promoting the formation of gaseous HONO. A detailed reaction mechanism is proposed that supports our experimental observations. Regarding the atmospheric implications, our results suggest that the NO₂ degradation on volcanic particles and the corresponding formation of HONO is expected to be significant during volcanic dust storms or after a volcanic eruption.