云、雨水酸度和离子浓度与其微物理参数的关系

本文1987年5-6月和1989年5-6月庐山地区的实测资料,分析了云、雨水酸度和离子浓度与其微物理量间的关系。结果表明,云、雨滴大小、含水量、谱宽等微物理量的演变直接影响着其酸度和离子浓度。     

庐山冬季雪景旅游气象景观预报

庐山雪景是庐山的著名气象景观之一。根据庐山气象台30年来的降雪观测资料,从旅游气象服务角度,介绍庐山雪景的山地天气条件特征,结合庐山具体山地降雪雪景景观的天气特点及山地气候环境特征,综合分析了庐山30年来降雪后雪景景观维持时间及不同降雪量下的降雪场次及其年分布特征,并描述了庐山雪景气象景观地域分布特点。     

Measurements of atmospheric hydroperoxides at a rural site in central Japan

Measurements of hydroperoxides (H₂O₂ and MHP) at ground level were made from 2012 to 2015 in Imizu City, Toyama Prefecture in central Japan. H₂O₂ and MHP concentrations ranged from 0.01 to 3.5 ppb and from below the level of detection (< 0.01 ppb) to 1.4 ppb, respectively. The concentrations of H₂O₂ and MHP were high in the summer and low in the winter. The H₂O₂ concentration was at its maximum in July and August, whereas the concentration of O₃ in the daytime was highest in May and June. The ratio of [H₂O₂]/[SO₂] presented clear seasonal variations. Many cases showed the condition of [H₂O₂] < [SO₂], called oxidant limitation especially in the cold months. Hydroperoxide concentrations in the rainwater were also high in the summer. The concentrations of MHP were much lower than those of H₂O₂ in the rain water. High concentrations of H₂O₂ (> 2.5 ppb) were detected in the summer during the inflow of air pollution. The concentrations of H₂O₂ were significantly high in July and August of 2013. The H₂O₂ was well correlated with the O₃ in July and August whereas there was no correlation between O₃ and H₂O₂ in May and June. There was a negative correlation between NO_X and H₂O₂.     

气流输送对北京大气污染物体积分数的影响

利用HYSPLIT后向轨迹模式和2004年8月—2007年12月NCEP再分析气象资料,计算每天15:00抵达北京地区10、100和500m高度上的后向气流轨迹.对整个研究时段、采暖季和非采暖季期间的后向气流轨迹分别进行聚类分析,得到这3个时段到达北京地区的主要后向气流轨迹聚类.其中整个研究时段的后向气流轨迹分成3个聚类,采暖季和非采暖季的后向气流轨迹都分成5个聚类.结合各段时间中国科学院大气物理研究所观测的大气污染物体积分数资料,分析不同时段气流输送作用对北京主要大气污染物体积分数的影响.发现采暖季和非采暖季北京气体污染物体积分数高值主要集中在来自风速较小的西北方气流聚类.采暖季污染物体积分数低值主要出现在偏北方向风速较大的后向气流轨迹聚类.非采暖季污染物体积分数低值主要出现在偏北低速气流聚类和西北向高速气流轨迹聚类中.从各时段污染物最值分布情况可以看出:在风速较大的后向气流轨迹聚类影响下,北京的污染物体积分数较低;途经了较严重工业排放地带的后向气流轨迹聚类会使北京气体污染物体积分数显著增高.此外,虽然非采暖季的大气污染物分布与气流输送的影响基本符合,但各聚类污染物分布结果与气流输送作用的影响存在偏差.     

碘化银地面发生器增雪水中Ag+与化学组分研究

为搞清实施人工影响天气后,所用碘化银催化剂是否对环境造成污染这一问题,利用2002年12月至2003年3月在北京尖子山,使用碘化银地面发生器在人工增雨雪试验中,对4次人工降雪过程所采集雪水样品进行了Ag 测定及其他化学组分分析。发现雪水中Ag 浓度在不同天气过程中变化明显,变化与催化剂数量间没有直接线性关系,所测的Ag 浓度远低于我国生活饮用水标准。雪水化学特征明显,雪水中阴离子浓度最高是SO42-、NO3-,阳离子Ca2 、NH4 浓度最高。与污染较重的雾水相比,雪水中的诸离子浓度远低于北京地区雾水所测值。     

北京奥运会期间NO2浓度降低原因分析

2002～2008年,北京市城区和近郊8月的NO2月均浓度大体呈现逐年下降趋势,其中前5年二者均以每年约10%的降幅下降,2008年发生显著下降,降幅达40%左右。利用嵌套网格空气质量模式系统(NAQPM/IAP),采用敏感性试验方法,评估了气象条件与污染控制措施对北京奥运会期间大气NO2浓度降低的影响,评估不同污染控制措施对NO2浓度降低的作用。研究结果表明,污染控制措施是NO2浓度降低的主要影响因素,其中面源的污染控制措施对于NO2浓度降低的作用最明显。     

Numerical study on the impacts of heterogeneous reactions on ozone formation in the Beijing urban area

The air quality model CMAQ-MADRID （Community Multiscale Air Quality-Model of Aerosol Dynamics, Reaction, Ionization and Dissolution） was employed to simulate summer O3 formation in Beijing China, in order to explore the impacts of four heterogeneous reactions on O3 formation in an urban area. The results showed that the impacts were obvious and exhibited the characteristics of a typical response of a VOC-limited regime in the urban area. For the four heterogeneous reactions considered, the NO2 and HO2 heterogeneous reactions have the most severe impacts on O3 formation. During the O3 formation period, the NO2 heterogeneous reaction increased new radical creation by 30%, raising the atmospheric activity as more NO→NO2 conversion occurred, thus causing the O3 to rise. The increase of O3 peak concentration reached a maximum value of 67 ppb in the urban area. In the morning hours, high NO titration reduced the effect of the photolysis of HONO, which was produced heterogeneously at night in the surface layer. The NO2 heterogeneous reaction in the daytime is likely one of the major reasons causing the O3 increase in the Beijing urban area. The HO2 heterogeneous reaction accelerated radical termination, resulting in a decrease of the radical concentration by 44% at the most. O3 peak concentration decreased by a maximum amount of 24 ppb in the urban area. The simulation results were improved when the heterogeneous reactions were included, with the O3 and HONO model results close to the observations.     

TERRAIN IMPACT ON THE PRECIPITATION OF LANDFALLING TYPHOON TALIM

The impact of terrains on the precipitation of landfalling typhoon Talim (2005) over mainland China is investigated using the fifth-generation Pennsylvania State University-National Center for Atmospheric Research Mesoscale Model. The simulated precipitation of simulated typhoon (the control) matches the observations closely. To compare with the control simulation, four sensitivity simulations were carried out in which terrains of Wuyi Mountain, Lushan, Dabieshan, and both Lushan and Dabieshan are completely removed respectively, but other surface properties were retained. It is found that the complex terrains of Wuyi Mountain, Lushan and Dabieshan have a significant impact on the rainfall intensity and distribution of Talim. As the terrains are removed, the rainfall is decreased very greatly and the rainfall in inland area is decreased much more than that in the coastal area. Besides, the rainfall distribution near the Lushan and Dabieshan is spread much more westward compared with the control simulation. Further analysis shows that the Wuyi Mountain would increase both the lower level air convergence and the upper level air divergence for Talim that just made landfall and thus it would contribute to the convection and increase rainfall intensity. It can be concluded that the terrains of Wuyi Mountain, Lushan and Dabieshan have obvious impacts on the Talim rainfall, and their impacts are different in various landfalling periods. The present study is a useful attempt to explore the influence of orography on the TCs in mainland China.     

利用WRF-Chem模拟研究京津冀地区夏季大气污染物的分布和演变

应用WRF—Chem（Weather Research and Forecasting Model with Chemistry）模式模拟研究了2007年8月京津冀地区近地面O3、NO2、PM2.5浓度的时空变化特征,将模拟结果与观测数据进行详细对比,结果表明,模式可以较好地模拟O3、PM2.5,浓度的空间分布和时间变化特征,成功再现了8月33和PM2.5的几次积累增加过程,其中O,的模拟值与观测值的相关系数为0．69～0．86,PM2.5的相关系数为0．44～0．49,但模式对NO2的模拟相对较差,相关系数为0．27～0．43。北京、天津地区为O3月均低值区,月均体积浓度约30×10^-9,渤海及京津冀以西地区O3月平均体积浓度可达60×10^-9;PM2,呈现南高北低的分布特征,变化范围为120～240μg／m3。14时月平均03体积浓度在北京、天津地区低于周边地区,约为60×10^-9;而PM2.5质量浓度在环渤海地区和河北南部较高,为100～120μg/m^3。8月17日北京出现一次典型的高浓度O,污染事件,14时北京地区温度达到33℃,O3体积浓度为80×10^-9～110×10^-9。在局地排放、化学反应和外来输送的共同作用下,渤海西岸和北岸PM2.5的质量浓度超过120μg／m3,其中二次气溶胶质量浓度为50～100μg／m3,一次排放人为气溶胶质量浓度为10～20μg／m3,海盐质量浓度为1～7μg／m3,二次气溶胶是该地区PM2.5的主要贡献者。     

我国地面O3、NOX、SO2背景值的观测研究

从1994年8月至1995年8月，在龙凤山、临安大气污染监测站和瓦里关大气本底基准观象台对O3、NOX及SO2首次进行了长期的连续观测。初步分析表明:3站地面O3的平均浓度、月际分布和日变化特征因地理环境、海拔高度和天气条件的不同，表现出明显的差异性。平均地面O3浓度，龙凤山为34.8×10-9,临安为39.1×10-9,瓦里关山为49.3×10-9,龙凤山和临安的月平均地面O3浓度分布较复杂，在6～7月和12月～1月较低，10月底～11月初较高。而在瓦里关山，月平均地面O3浓度变化较平稳，6月份最大，12月最小。龙凤山和临安地面O3平均日变化量较大，下午浓度最高，清晨最小；而瓦里关山地面O3平均日变化较小，上午浓度略低；NOX和SO2的分布具有明显的局地性特征，在龙凤山，临安和瓦里关山，3站的总平均浓度分别为2.7×10-9（NOX）和0.7×10-9(SO2),8.1×10-9(NOX)和16.1×10-9（SO2），0.04×10-9（NOX）和0.15×10-9（SO2）。     

青岛大气臭氧及其前体物时间变化与污染特征

利用2003年12月—2005年3月青岛八关山观测资料,分析大气中O3、NOX和CO浓度时间变化规律与影响因素,探讨O3及其主要前体物NOX、CO间复杂的相互作用及相关关系。结果表明:青岛NO2日平均浓度年超标率为25%;受光化学反应及大气运动等影响,NOX与CO浓度为冬季高、夏季低,O3与之相反;NOX与CO浓度日变化呈双峰型分布,日间高于夜间;O3浓度峰值出现于午后(滞后于NOX约5 h),阴雨天夜间浓度出现回升。经滞后相关分析,NOX对O3浓度变化的累积效应作用时间为5—6 h;O3与NO、NO2浓度比值可较明显地验证出辐射强度与尾气排放对青岛及其他地区污染特征的影响。青岛CO与NOX比值在不同天气条件下维持在10.0左右,可用于定性估计其大气污染特征。     

温带森林土壤溶液溶解性N2O和CO2含量特征及其影响机制

利用陶瓷头土壤溶液收集器采集2006年7月～2007年8月问长白山阔叶红松天然林不同深度(15cm和60 cm)土壤溶液,探讨应用气液萃取平衡-气相色谱法测定森林土壤溶液中溶解性气体N_2O和CO_2浓度的可行性,并利用此方法研究林地不同深度土壤溶液中两种气体含量特征及其影响机理.研究结果显示观测期内林地15 cm和60 cm深度土壤溶液中溶解性CO_2浓度的变化范围分别为5.26～10.71μg·mL~(-1)(C)和3.13～6.16 μg·mL~(-1)(C),溶解性N_2O浓度的变化范围分别为2.44～13.40 ng·mL~(-1)(N)和3.23～27.98 ng·mL~(-1)(N).阔叶红松天然林土壤溶液中溶解性CO_2和N_2O浓度均呈现出明显的季节性变化.春融后的降水促进了土壤溶液中溶解性N_2O产生,尤其在60 cm深度.与60 cm深度相比,林地15 cm深度溶液中溶解性CO_2浓度的季节性变化更明显,尤其在植物生长旺季.逐步回归分析显示,水溶性有机碳含量可以解释林地不同深度溶液中溶解性CO_2浓度变化的29%;水溶性有机氮含量可以解释林地60 cm深度溶解性N_2O浓度变化的34%.因此,水溶性有机碳和有机氮分别是长白山阔叶红松林土壤溶液溶解性CO_2和N_2O形成的重要因子.同时研究结果表明本文实验方法对于测定林地不同深度土壤溶液中溶解性N_2O和CO_2含量均有较好的适用性,连续三次萃取后所获得的气体浓度可有效反映溶液中的实际气体浓度.     

Measurements of ozone and its precursor nitrogen dioxide and crop yield losses due to cumulative ozone exposures over 40 ppb (AOT40) in rural coastal southern India

Measurements of ground level ozone (O₃), nitrogen dioxide (NO₂) and meteorological parameters (air temperature, relative humidity and wind speed and direction) has been made for 3 years from March 2007 to February 2010 at Nagercoil (8.2°N, 77.5°E, 23 m above sea level), an equatorial rural coastal site of southern India. The monthly average of daytime maximum of O₃ concentrations ranged from 28 to 50 parts per billion (ppb) with an annual average of 19.8 ppb. Similarly, monthly average of NO₂ concentration ranged from 3.4 ppb to 7.7 ppb with an annual average of 5.3 ppb. The monthly variation of meteorological parameters shows the little changes being a coastal site. The estimated summer crops yield losses by 1.1–15.6 % from present O₃ concentration level associated with AOT40 index 3.1–5 ppm h.     

利用GOME卫星资料分析北京大气NO2污染变化

利用GOME (Global Ozone Monitoring Experiment, 全球臭氧监测实验) 1996年1月—2002年12月NO₂对流层柱浓度月平均卫星遥感资料以及根据北京市2001年1月1日—2002年12月31日NO₂污染指数数据计算出的地面NO₂日均质量浓度值, 分析了北京市城市大气NO₂污染变化的季节变化特征以及年际变化, 并将2001年1月—2002年12月北京上空GOME NO₂对流层柱浓度月平均值变化与北京市地面NO₂日均质量浓度月平均值变化进行了比较, 结果表明两者随时间的变化趋势具有较好的一致性, 据此可以利用GOME NO₂对流层柱浓度月平均卫星遥感资料来分析特定区域大气NO₂的季节变化和年际变化。     

蒙特卡罗不确定性分析在O3模拟中的初步应用

利用蒙特卡罗不确定性分析方法,分析了嵌套网格空气质量模式系统(NAQPMS/IAP)中154个模式输入变量不确定性对臭氧模拟的影响,量化了模式在北京奥运会期间臭氧模拟的不确定性,并确定出了主要不确定性因子。结果表明:(1)在奥运会期间(2008年8月8日～2008年8月24日),北京城区臭氧模拟的平均不确定性为19ppb,不确定性存在明显的日变化特征,白天不确定性大,夜间不确定性小。(2)在白天,北京城区近地层臭氧模拟最重要的不确定性来源是局地前体物排放,其次是NO2光解系数、风向、北京周边前体物排放和垂直扩散系数。另外,地面约150m以上,对臭氧模拟影响最大的不确定性因子是风向和北京周边前体物排放;夜间,北京城区近地层臭氧模拟的最大不确定性来源是局地NOx排放和垂直扩散系数。     

Seasonal variation of gaseous HNO3 and NH3 at a Tropical Savannah site

Gaseous nitric acid and ammonia were sampled with annular denuders at a forest savannah site from April to December 1987. The analysis of the extract was made spectrophotometrically and by a selective electrode for NO₃ ^– and NH₄ ⁺, respectively. Higher concentrations were observed during the vegetation burning period at the end of the dry season. In the studied savannah area, large soil emissions of NO occur during the rainy season, although very low concentrations of HNO₃ (0.035 ppb) and also of particulate NO₃ ^– (0.43 g m^-3) were observed; it is likely that NO_x are lost by fast vertical transport to the upper troposphere. During the nonburning period, the average concentration of NH₃ was 2.7 ppb, which is much lower than values given in the literature for the tropical America atmosphere. The concentrations of HNO₃ and NH₃ were always below the values needed to produce ammonium nitrate aerosols.     

On the Spatial Distribution and Seasonal Variation of Lower-Troposphere Ozone over Europe

Surface ozone data from 25 Europeanlow-altitude sites and mountain sites located between79°N and 28°N were studied. The analysiscovered the time period March 1989–February 1993.Average summer and winter O₃ concentrations inthe boundary layer over the continent gave rise togradients that were strongest in the north-west tosouth-east direction and west-east direction, respectively. WintertimeO₃ ranged from 19 to 27 ppbover the continent, compared to about 32 ppb at thewestern border, while for summer the continentalO₃ values ranged between 39 and 56 ppb and theoceanic mixing ratios were around 37 ppb. In the lowerfree troposphere average wintertime O₃ mixingratios were around 38 ppb, with only an 8 ppbdifference between 28°N and 79°N. For summerthe average O₃ levels decreased from about 55 ppbover Central Europe to 32 ppb at 79°N. Inaddition, O₃ and O_x(= O₃ + NO₂)in polluted and clean air were compared. Theamplitudes of the seasonal ozone variations increasedin the north-west to south-east direction, while thetime of the annual maximum was shifted from spring (atthe northerly sites) to late summer (at sites inAustria and Hungary), which reflected the contributionof photochemical ozone production in the lower partsof the troposphere.     

Chemical character of precipitation and related particles and trace gases in the North and South of China

Rainwater samples were collected at four sites, including Beijing and Mazhuang Town in the north of China, Shenzhen and Mangdang Mountain in the south of China. Character of atmospheric particles and gases were also measured at Mazhuang Town and Mangdang Mountain. Both of Beijing and Shenzhen are urban sites; Mazhuang Town and Mangdang Mountain are rural and remote sites respectively. The atmospheric pollution at rural plain site in the north of China was more serious than that at remote mountain site in the south of China. At Beijing, Mazhuang Town, Shenzhen and Mangdang Mountain the average pH values in rainwater were 6.02, 5.97, 4.72 and 4.81, respectively and the concentrations of total ions in rainwater were 1454, 1125, 187 and 191 μeq/l, respectively. While the acidity of the rain was higher in the south than that in the north, the rainwater in the north of China was more severely polluted than that in the south. The major acidic ion in the rainwater is SO₄^2-, and NH₄⁺ is the most important neutralizing ion in rainwater at the four sites, followed by Ca²⁺. The amounts of organic acid in precipitation were compared with other sites in the world. The ratios of organic acid to total free acid in rainwater at Mangdang Mountain was 13.8% and the influence of organic acid on acidity of rainwater at mountain site in the south of China is more important. The variation of atmospheric particles, gases and components in rainwater and cloud-fog water during special rain and cloud-fog events was discussed. The importance of washout process varied with atmospheric species. The impacts of rainfall, rain duration time and wind speed on wash-out process were estimated by regression analysis.     

POPCORN: A Field Study of Photochemistry in North-Eastern Germany

The intensive field study POPCORN (Photo-Oxidant Formation by Plant Emitted Compounds and OH Radicals in North-Eastern Germany) was carried out in a rural area of North-Eastern Germany during August 1994. An overview of the objectives, measurements and major results of this campaign is presented. Measurements of a set of relevant atmospheric trace compounds, including the hydroxyl radical, along with meteorological data were performed to increase the understanding of OH radical chemistry and photo-oxidant formation. Additionally, plant emissions and the exchange of trace gases between a maize field and the atmosphere were investigated. Budgets of selected trace gases were calculated to assess the relative importance of local sources, chemistry or transport. Intercomparisons between measurement techniques were a central issue of POPCORN and included measurements of OH, hydrocarbons, formaldehyde, photolysis frequencies and vertical fluxes. OH radical concentrations were measured simultaneously by LIF (Laser Induced Fluorescence) and DOAS (Differential Optical Absorption Spectroscopy). Both methods showed good agreement. Maximum OH concentrations were around 107 cm–3 and the diurnal cycles closely followed the rate of primary production via ozone photolysis. Generally, the trace gas composition during POPCORN was characterized by relatively low concentrations of most compounds, e.g. CO: 85–200 ppb, ethane: 0.6–2 ppb, and moderate NOx levels: 0.5–5 ppb (at noontime). Concentrations of individual biogenic volatile organic compounds (VOC) were mostly well below 100 ppt. However, formaldehyde and acetaldehyde which partly originate from biological sources were observed at mixing ratios of some ppb.     

Precipitation chemistry and ozone and sulfate concentrations in the ocean atmosphere observed by multi-year cruising in East Asia and West Oceania (35°N–35°S, 100–135°E) in August and September

A comprehensive study on the chemistry of deposition and the concentration of tropospheric ozone and particulate sulfate in the ocean atmosphere was carried out for the data sets in 1990’s. It is important to study the atmospheric situation over the past years as well as the latest, especially in the East Asian region where emission amount of anthropogenic air pollutants have increased year by year due to rapid economic growth. The survey was conducted for 5 years in East Asia and West Oceania (35°N–35°S, 100–135°E) in August and September in 1990’s. The purpose of the survey was to study and understand the chemistry of deposition and the concentration of tropospheric ozone and particulate sulfate in the ocean atmosphere comprehensively in one project. Rainfall over the ocean was insufficiently neutralized. Gas and aerosol over the ocean were mature, i.e., well-mixed, during the period of the transportation. The characteristic latitudinal dependence was observed in the tropospheric ozone concentration, namely, higher in the southern hemisphere and lower in the northern hemisphere (approximately 25 ppb in the 10–40°S region and 5–15 ppb in the 20–40°N region). On the other hand, high concentrations of tropospheric ozone of over 30 ppb were observed in the northern hemisphere, which was attributable to the long-range transportation. The TSP concentration was approximately under the level of 40 μg m^?3 irrespectively of the latitude; in contrast, the nss-SO₄ ^2- concentration showed a clear latitudinal dependence, i.e., higher in the northern hemisphere and lower in the southern hemisphere. The background levels of the nss-SO₄ ^2- concentration were approximately 0.5 μg m^?3 in the 10–40°S region and 2–3 μg m^?3 and 4–5 μg m^?3 in the 0–20°N and 20–40°N regions, respectively.