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1.
The surface level measurements of O3, CO, CH4 and light NMHCs were made at eight different rural sites in the central part of India during February, 2004. The online analyzer was used for in-situ measurement of O3 while air samples were collected for the analyses of CO, CH4 and NMHCs using the gas chromatography techniques. The average mixing ratios of O3, which were in the range of 60–90 ppbv, are significantly higher compared to the typical values reported for urban sites of India. The increase rates of O3 in the forenoon hours were estimated to be in the range of about 8.8–10 ppbv h−1. The slopes of ∆O3/∆CO, which is an indicator of the efficiency of photochemical production, were in the range of 0.24–0.33 ppbv ppbv−1. However, levels of primary pollutants e.g., NMHCs, CO, etc. at these sites were much lower than urban sites, but higher compared to previously observed values surrounding marine region of India. The estimated ratios of NMHCs and CO indicate fossil fuel combustion process as the dominant source of primary pollutants in this corridor.  相似文献   

2.
The fractions of local traffic (LT), urban background (UBG) and regional background (RBG) of the particle pollution at a traffic-influenced kerbside in Dresden, Germany, were determined by measurements of size-segregated mass concentration, chemical composition and particle size distributions in a network of five measurement stations partly existing and partly set up for this study. Besides the kerbside station, one urban background site and three rural sites were included in the study. Using data from these different sites, the LT, UBG, and RBG contributions were calculated, following the approach of Lenschow et al. (2001). At the kerbside site, 19% of the total number concentration (DpSt = 10–600 nm) could be attributed to the RBG, 15% to the UBG, and 66% to the LT immediately nearby. Particle mass concentrations up to Dpaer = 420 nm RBG amounts to 68%, UBG to 21%, and LT only to 11%. Highest mass concentrations were observed at all stations in autumn and winter during easterly inflow directions. The local traffic fraction of PM10 mass at the kerbside station was found to be 30% for westerly inflow, but only 7% for southeasterly inflow due to the dominating transport fraction from up to 80% of the particle mass at this inflow direction. Size-resolved investigation showed the main fractions in both the particle size ranges of Dpaer = 0.42 to 1.2 and 0.14 to 0.42 μm at all stations. The main components sulphate, ammonium and total carbon showed higher concentrations at south-eastern/eastern inflow in autumn at all stations, while nitrate at the kerbside and urban background site was higher during westerly inflow in winter. The chemical composition at the regional background site at westerly inflow (12% nitrate, 8% sulphate, 11% total carbon) was significantly different from that at easterly inflow (3% nitrate, 15% sulphate, 22% total carbon). The prevailing part of the ionic mass was always found in the fine particle range of Dpaer = 0.14 to 1.2 μm at all stations. For all inflow directions highest total carbon concentrations were observed at the kerbside station, especially in the ultra-fine size range of Dpaer = 0.05 to 0.14 μm with up to 30% of the whole carbon. PAH concentrations were always higher at south-eastern/eastern inflow especially during wintertime. Trace metal components and silicon were found mainly in the coarse mode fraction at the kerbside resulting from abrasion or resuspension.  相似文献   

3.
Significant quenching of fluorescence by Cu in rainwater samples from southeastern North Carolina demonstrates that chromophoric dissolved organic matter (CDOM) is an effective ligand for Cu in rainwater. A strong inverse correlation between the decrease in fluorescence upon Cu addition and CDOM abundance suggests the presence of excess binding sites for Cu in high CDOM samples. Electroanalytical studies indicate that CDOM extracted from C18 cartridges formed Cu complexes with concentrations and conditional stability constants similar to ligands found in ambient rainwater. When authentic rainwater samples were photolyzed with simulated sunlight both photoproduction and photodestruction of ligands were observed, suggesting the photochemical response of Cu-complexing ligands in rainwater is the result of two competing reactions. The rate of CDOM photobleaching was directly related to changes in strong ligands (KCuL ∼ 1015) whereas weaker ligands (KCuL < 1013) were not correlated, suggesting the photolabile CDOM resides in the strong ligand class. A photolysis study comparing filtered and unfiltered rainwater samples indicated that Cu-complexing ligands adsorbed onto or otherwise associated with particles are photodegraded much more rapidly than dissolved ligands. Photolysis with UV radiation appears to be most effective at engendering changes in Cu ligands, however a significant photochemical response was also observed when samples were exposed to photosynthetically active radiation with wavelengths greater than 400 nm. Results from this study demonstrate that complexation of Cu by CDOM has important ramifications for controlling both the speciation of the metal and the reactivity of CDOM in rainwater.  相似文献   

4.
The present study was carried out between October 2003 and September 2004 at an urban background station near the Mediterranean coast in southeastern Spain. The sulfate and nitrate content was determined in 332 PM10 and PM2.5 daily samples. The results show that the seasonal variation of nitrate measured in PM10 does not correspond with what has been observed at other locations in the Iberian Peninsula, where the minima are reached during the summer months due to decomposition of ammonium nitrate at high temperatures. The recorded levels of PM10 nitrate were slightly higher in summer due to an increase in the concentrations of coarse mode nitrate. On the contrary, both the concentrations and the percentages of nitrate in PM2.5 were lowest from June to September. The sulfate levels in both PM10 and PM2.5 were maxima in summer because the oxidation rate of SO2 increases with solar radiation. An elevated correlation (0.72 < r < 0.92) between the monthly average concentrations and percentages of sulfate and solar radiation has been found. We have also investigated the influence that Saharan dust intrusions and high pollution episodes have upon the sulfate and nitrate concentrations. Both types of events increased NO3− and SO42− levels, particularly the high pollution episodes.  相似文献   

5.
利用2019年8月13日—9月30日江苏省13个设区市离线监测的VOCs数据,对江苏省城区VOCs污染特征及其关键活性组分进行分析研究.结果表明,江苏省逐日VOCs的体积分数范围为8.83×10-9~45.11×10-9,表现为烷烃 > 芳香烃 > 烯烃 > 炔烃.江苏省13个设区市VOCs的体积分数为7.85×10-9~30.52×10-9,徐州市VOCs最高,这与徐州市监测点位置分布及其工业结构相关.全省13个设区市臭氧浓度处于优、良、轻度污染和中度污染时,VOCs总体积分数分别为14.96×10-9、17.96×10-9、25.85×10-9和25.11×10-9,臭氧浓度处于污染状态时的VOCs高于优、良状态,且炔烃占比随着臭氧污染程度的加重呈升高趋势,表明现阶段臭氧生成与人类活动关系密切.通过加权的方式筛选出间/对二甲苯、乙烯、甲苯、丙烯、异戊二烯、邻二甲苯等物种,它们是目前对江苏省城区影响程度较大且影响范围较广的关键活性物种.  相似文献   

6.
In the present study, an attempt has been made to examine the governing photochemical processes of surface ozone (O3) formation in rural site. For this purpose, measurements of surface ozone and selected meteorological parameters have been made at Anantapur (14.62°N, 77.65°E, 331 m asl), a semi-arid zone in India from January 2002 to December 2003. The annual average diurnal variation of O3 shows maximum concentration 46 ppbv at noon and minimum 25 ppbv in the morning with 1σ standard deviation. The average seasonal variation of ozone mixing ratios are observed to be maximum (about 60 ppbv) during summer and minimum (about 22 ppbv) in the monsoon period. The monthly daytime and nighttime average surface ozone concentration shows a maximum (55 ± 7 ppbv; 37 ± 7.3 ppbv) in March and minimum (28 ± 3.4 ppbv; 22 ± 2.3 ppbv) in August during the study period. The monthly average high (low) O3 48.9 ± 7.7 ppbv (26.2 ± 3.5 ppbv) observed at noon in March (August) is due to the possible increase in precursor gas concentration by anthropogenic activity and the influence of meteorological parameters. The rate of increase of surface ozone is high (1.52 ppbv/h) in March and lower (0.40 ppbv/h) in July. The average rate of increase of O3 from midnight to midday is 1 ppbv/h. Surface temperature is highest (43–44°C) during March and April months leading to higher photochemical production. On the other hand, relative humidity, which is higher during the rainy season, shows negative correlation with temperature and ozone mixing ratio. It can be seen that among the two parameters are measured, correlation of surface ozone with wind speed is better (R 2=0.84) in compare with relative humidity (R 2=0.66).  相似文献   

7.
北京一次持续霾天气过程气象特征分析   总被引：6，自引：0，他引：6       下载免费PDF全文
2013年1月10-14日,北京平原地区出现了水平能见度在2 km以下、以PM2.5为首要污染物、空气质量持续5 d维持在重度以上污染水平的霾天气。综合分析此次霾天气过程的天气形势、北京地区常规和加密气象资料以及城郊连续观测的PM2.5浓度资料。结果表明：此霾过程期间,北京高空以平直纬向环流为主,受西北偏西气流控制,没有明显冷空气南下影响北京地区,地面多为不利于污染物扩散和稀释的弱气压场;大气层结稳定、风速小(日平均风速小于2 m·s-1)、相对湿度较大（日平均相对湿度在70 %以上）、逆温频率高强度大,边界层内污染物的水平和垂直扩散能力差;北京城区及南部的京津冀地区人类活动排放污染物强度大,在相对稳定和高湿的天气背景下,受地形和城市局地环流的影响,北京本地污染物累积和区域污染物输送以及PM2.5细粒子在高湿条件下的物理化学转化等过程共同作用造成此次北京城区及平原地区污染物浓度快速增长并持续偏高,高浓度PM2.5对大气消光有显著影响,造成低能见度和持续霾天气。  相似文献   

8.
过氧乙酰硝酸酯（PAN）是由VOCs和NOx的光化学反应生成的一种典型二次污染物,比O3更适合作为光化学污染的指示剂.2019年6—10月对浙江中部盆地金华市大气中PAN进行了在线监测,并对影响其体积分数变化的因素进行了分析,同时还分析了一次典型的光化学污染过程.结果表明,观测期间PAN的平均体积分数为0.656×10-9,最高体积分数为4.348×10-9,日均体积分数水平在0.130×10-9~2.203×10-9之间.PAN日变化特征显著,9月为明显的双峰变化,其他月份均为单峰.受气象条件的影响,夏季的污染程度显著低于秋季.9月27—30日典型污染时段内,PAN的小时均值是整个观测期均值的2.8倍,污染以本地积累为主.前体物浓度水平差异与去除机制的不同是影响PAN和O3相关性的重要因素,此外NO/NO2的比值是影响PAN生成速率的重要因素,PAN的峰值基本出现在NO/NO2比值较低的时段.在生成PAN的VOCs物种中,丙烷、乙烷和间/对二甲苯所占比例较大.  相似文献   

9.
In this study, an improved and complete secondary organic aerosols (SOA) chemistry scheme was implemented in the CHIMERE model. The implementation of isoprene chemistry for SOA significantly improves agreement between long series of simulated and observed particulate matter concentrations. While simulated organic carbon concentrations are clearly improved at elevated sites by adding the SOA scheme, time correlation are impaired at low level sites in Portugal, Italy and Slovakia. At several sites a clear underestimation by the CHIMERE model is noticed in wintertime possibly due to missing wood burning emissions as shown in previous modeling studies. In Europe, the CHIMERE model gives yearly average SOA concentrations ranging from 0.5 μg m  − 3 in the Northern Europe to 4 μg m  − 3 over forested regions in Spain, France, Germany and Italy. In addition, our work suggests that during the highest fire emission periods, fires can be the dominant source of primary organic carbon over the Mediterranean Basin, but the SOA contribution from fire emissions is low. Isoprene chemistry has a strong impact on SOA formation when using current available kinetic schemes.  相似文献   

10.
利用北京市房山区良乡镇和琉璃河镇内的区域自动气象站和环境监测站观测数据,对2013年至2015年PM_(2. 5)、PM_(10)、NO_2、SO_2、CO 5种大气污染物浓度变化特征进行了统计分析。结果显示,近3年来,两个镇综合污染物指数呈现逐年下降趋势,各污染物对房山区整体大气污染的贡献率从大至小依次为PM_(2. 5)、PM_(10)、SO_2、NO_2、CO,PM_(2. 5)已取代传统大气污染物SO_2成为房山区的主要大气污染贡献体。两个站点各污染物浓度均表现出明显的季节、月、日变化特征。在不同季节条件下,局地气象要素与污染天气发生概率之间有着很好的相关关系。因此,可根据气象要素分级方法找出各季节污染天气发生时最敏感的气象因素,为局地污染天气预报提供参考指标,也为防范空气污染、制定科学的综合管理措施提供科学参考。  相似文献   

11.
Summary.  Mesoscale convective precipitation systems in the Alpine region are studied by analyzing radar and rain gauge data. The data from weather radars in Austria, France, Germany, and Switzerland are combined into a composite. Availability of radar data restricts the study mainly to the northern part of the Alpine region. Mesoscale convective systems (MCS) occur often in this region and are comparable to large systems observed in the USA. Seven precipitation events lasting one to six days from the years 1992–1996 are examined in detail. They all moved west to east and showed no diurnal preference in formation or dissipation. They reach sizes of 2 − 6 · 104 km2. MCS with leading-line trailing-stratiform structure tended to be larger and more intense. A 25-year set of rain gauge data indicates that a giant MCS (covering more than 4 · 104 km2 with more than 30 mm/day) occurs every 6 years in the northern Alpine region. MCS occur more frequently in the southern Alpine region. Received February 25, 1999/Revised June 29, 1999  相似文献   

12.
Characteristics of carbonyl compounds in ambient air of Shanghai,China   总被引：3，自引：0，他引：3  
The levels of carbonyl compounds in Shanghai ambient air were measured in five periods from January 2007 to October 2007 (covering winter, high-air-pollution days, spring, summer and autumn). A total of 114 samples were collected and eighteen carbonyls were identified. Formaldehyde, acetaldehyde and acetone were the most abundant carbonyls and their mean concentrations of 19.40 ± 12.00, 15.92 ± 12.07 and 11.86 ± 7.04 μg m−3 respectively, in the daytime for five sampling periods. Formaldehyde and acetaldehyde showed similar diurnal profiles with peak mixing ratios in the morning and early afternoon during the daytime. Their mean concentrations were highest in summer and lowest in winter. Acetone showed reversed seasonal variation. The high molecular weight (HMW, ≥C5) carbonyls also showed obvious diurnal variations with higher concentrations in the daytime in summer and autumn, while they were all not detected in winter. Formaldehyde and acetaldehyde played an important role in removing OH radicals in the atmosphere, but the contribution of acetone was below 1%. The carbonyls levels in high-air-pollution days were reported. More carbonyl species with higher concentrations were found in high-air-pollution days than in spring. These carbonyls were transported with other pollutants from north and northwest in March 27 to April 2, 2007 and then mixed with local sources. Comparing with Beijing and Guangzhou, the concentrations of formaldehyde and acetaldehyde in Shanghai were the highest, which indicated that the air pollution in Shanghai was even worse than expected.  相似文献   

13.
Summary  Three cyclones developing between 28 August and 6 September 1995 were studied with respect to the temporal evolution of their water budget components. The cyclones were simulated with the regional model REMO. Water budget values were determined from hourly model output for circle areas with 500 km radius around the pressure minimum. The results show a maximum liquid water path of about 0.12 kg m−2 and a maximum ice water path of 0.16 kg m−2. In the vertical cloud structure the medium cloud layer disappears at the end of the life cycle for all three cyclones. The release of precipitation onto the Baltic Sea drainage basin is different for each cyclone. It lies between 13 and 22 · 1012 kg. This is about 50% of the total precipitation in the whole area for the strongest cyclone and 65% for the others. The P — E (precipitation minus evaporation) is 15 · 1012 kg for two of the cyclones and 10 · 1012 kg for the third one. Received August 7, 2000 Revised March 19, 2001  相似文献   

14.
In this experimental study, rate constants were measured for the reactions of ozone with 13 polycyclic aromatic hydrocarbons (PAHs) adsorbed on different types of particles. Graphite and silica were chosen to model, respectively, carbonaceous and mineral atmospheric particles. The pseudo-first order rate constants were obtained from the fit of the experimental decay of particulate PAH concentrations versus time. Second order rate constants were calculated considering the ozone gaseous concentration. At room temperature, rate constants varied, in the case of graphite particles, between (1.5 ± 0.5) × 10−17 and (1.3 ± 0.7) × 10−16 cm3 molecule−1 s−1 for chrysene and dibenzo[a,l]pyrene, respectively, and, in the case of silica particles, between (1.5 ± 0.3) × 10−17 and (1.4 ± 0.3) × 10−16 cm3 molecule−1 s−1 for fluoranthene and benzo[a]pyrene, respectively. Different granulometric parameters (particle size, pore size) and different PAH concentrations were tested in the case of silica particles. Heterogeneous reactions of ozone with particulate PAHs are shown to be more rapid than those occurring in the gas-phase, and may be competitive with atmospheric photodegradation.  相似文献   

15.
PM2.5 is a big issue as it is considerably more harmful than other sizes of particulate matter. World Health Organization (WHO) recommends 25 μg m?3 as the daily average concentration, and 10 μg m?3 per day as an annual average. To keep up with global trends, it is first necessary to understand the current status and characteristics of PM2.5 concentrations in Korea. Using the PM2.5 data measured by Seoul Metropolitan City from November 2005 to March 2012, the author analyzed its statistical characteristics and correlations with other air pollutants. For the time period from 2005 to 2012, the annual average concentration of PM2.5 was 27 μg m?3, three times the WHO standard. Also, the daily average PM2.5 concentration of 215 days per year also exceeded the WHO standard. However, the number days exceeding the Korean daily average standard of 50 μg m?3 to be enacted in 2014 was only three. PM2.5 concentration had a high correlation (r = 0.84) with PM10, and also showed high correlations with gaseous pollutants, such as SO2, NO2, and CO, but not O3. This study suggests that the Korean government should strengthen their standard to match the criteria used by WHO.  相似文献   

16.
Both aerosol and rainwater samples were collected and analyzed for ionic species at a coastal site in Southeast Asia over a period of 9 months (January–September 2006) covering different monsoons. In general, the occurrence and distribution of ionic species showed a distinct seasonal variation in response to changes in air mass origins. Real-time physical characterization of aerosol particles during rain events showed changes in particle number distributions which were used to assess particle removal processes associated with precipitation, or scavenging. The mean scavenging coefficients for particles in the range 10–500 nm and 500–10 μm were 7.0 × 10−5 ± 2.8 × 10−5 s−1 and 1.9 × 10−4 ± 1.6 × 10−5 s−1, respectively. A critical analysis of the scavenging coefficients obtained from this study suggested that the wet removal of aerosol particles was greatly influenced by rain intensity, and was particle size-dependent as well. The scavenging ratios, another parameter used to characterize particle removal processes by precipitation, for NH4 +, Cl−, SO4 2−, and NO3 − were found to be higher than those of Na+, K+, and Ca2+ of oceanic and crustal origins. This enrichment implied that gaseous species NH3, HCl, and HNO3 could also be washed out readily. These additional sources of ions in precipitation presumably counter-balanced the dilution effect caused by high total precipitation volume in the marine and tropical area.  相似文献   

17.
Aerosol and rain samples were collected between 48°N and 55°S during the KH-08-2 and MR08-06 cruises conducted over the North and South Pacific Ocean in 2008 and 2009, to estimate dry and wet deposition fluxes of atmospheric inorganic nitrogen (N). Inorganic N in aerosols was composed of ~68% NH4+ and ~32% NO3– (median values for all data), with ~81% and ~45% of each species being present on fine mode aerosol, respectively. Concentrations of NH4+ and NO3− in rainwater ranged from 1.7–55 μmol L−1 and 0.16–18 μmol L−1, respectively, accounting for ~87% by NH4+ and ~13% by NO3− of total inorganic N (median values for all data). A significant correlation (r = 0.74, p < 0.05, n = 10) between NH4+ and methanesulfonic acid (MSA) was found in rainwater samples collected over the South Pacific, whereas no significant correlations were found between NH4+ and MSA in rainwater collected over the subarctic (r = 0.42, p > 0.1, n = 6) and subtropical (r = 0.33, p > 0.5, n = 6) western North Pacific, suggesting that emissions of ammonia (NH3) by marine biological activity from the ocean could become a significant source of NH4+ over the South Pacific. While NO3− was the dominant inorganic N species in dry deposition, inorganic N supplied to surface waters by wet deposition was predominantly by NH4+ (42–99% of the wet deposition fluxes for total inorganic N). We estimated mean total (dry + wet) deposition fluxes of atmospheric total inorganic N in the Pacific Ocean to be 32–64 μmol m−2 d−1, with 66–99% of this by wet deposition, indicating that wet deposition plays a more important role in the supply of atmospheric inorganic N than dry deposition.  相似文献   

18.
Summary Using digitized IR images from the European satellite Meteosat, 153 squall lines (SLs) were observed over Western Africa during July, August and September 1986 and 87. The SL mean rainfall volume was computed using the daily rainfall amounts of more than 800 raingauges: 15 km3 in 1986 and 22.5 km3 in 1987. A mean amount of 15 mm was collected per rainy episode at a given station, however, as only about half of the stations situated under a SL experienced a rainy episode, the rainfall amount averaged along the total SL’s swath was 6.8 mm. With the help of the 8 daily Meteosat slots the SL’s area daily variation could be estimated: namely a minimum around noon and a maximum around midnight. Using the SLs displacements (east–west) one had access to the daily variation of the rainfall volume, a minimum in the morning and a maximum toward the end of the afternoon, as already found by several authors who used Meteosat images.  相似文献   

19.
This paper presents samples of Saharan dust outbreak affecting the Mediterranean Tunisian coasts and its impact on PM10 (Particles with an aerodynamic diameter below 10 µm) surface concentrations measured at seven monitoring stations during summer 2006. During the events, the daily PM10 levels at all stations exceeded EU and Tunisian air quality standard limits which are equal to 50 µg/m3. The maximum values ranged from 200 µg/m3 to 300 µg/m3 depending on the monitoring station. The impact is even more dramatic on PM10 hourly concentrations leading to maximum hourly peaks ranging from 400 µg/m3 to 850 µg/m3 again depending on the monitoring station (industrial or residential, traffic and commercial). Comparison between backward air masses trajectories reaching Tunisian coasts and satellite imageries vis-à-vis the PM10 hourly concentrations measured at the monitoring stations during 2006 evidenced the influence of the Saharan dust outbreaks on surface concentrations. The origin of the air masses is found to be from South-West direction under the influence of air masses from the Algerian Saharan desert.  相似文献   

20.
Ambient respirable particles (PM10; aerodynamic diameter ≤10 μm) collected in a tropical urban environment (Delhi, India) during December 2008-November 2009 were characterized with respect to 16 US EPA priority polycyclic aromatic hydrocarbons (PAHs) and 8 major and trace metals (Fe, Mn, Cd, Cu, Ni, Pb, Zn and Cr). Concentrations of Σ16PAHs (annual mean: 74.7 ± 50.7 ng m−3, range 22.1–258.4 ng m−3) and most metallic species were at least an order of magnitude greater than values reported from similar locations worldwide. Seasonal variations in Σ16PAHs were significant (p < 0.001) with highest levels in winter while crustal and anthropogenic metals showed significant but mutually opposite seasonal dependence. Statistically significant associations were observed between chemical species and various meteorological parameters. The PAH profile was dominated by combustion-derived large-ring species (~85%) that were essentially local in origin. Principal component analysis–multiple linear regression (PCA-MLR) apportioned four sources: crustal dust (73%), vehicular emission (21%), coal combustion (4%) and industrial emission (2%) that was further validated by hierarchical cluster analysis (HCA). Temporal trend analysis showed that crustal sources were predominant in summer (p < 0.05) while the remaining sources were most active in winter. Summertime intrusions of Saharan dust were identified with the help of aerosol maps and air parcel backward trajectories. Inhalation cancer risk assessment showed that up to 3,907 excess cancer cases (357 for PAHs, 122 for Cd, 2040 for Cr (VI) and 1387 for Ni) are likely in Delhi considering lifetime inhalation exposure to these chemicals at their current concentrations.  相似文献   

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