首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 687 毫秒
1.
Continuous in-situ measurements of surface ozone (O3), carbon monoxide (CO) and oxides of nitrogen (NOx) were conducted at Udaipur city in India during April 2010 to March 2011. We have analyzed the data to investigate both diurnal and seasonal variations in the mixing ratios of trace gases. The diurnal distribution of O3 showed highest values in the afternoon hours and lower values from evening till early morning. The mixing ratios of CO and NOx showed a sharp peak in the morning hours but lowest in the afternoon hours. The daily mean data of O3, CO and NOx varied in the ranges of 5–51 ppbv, 145–795 ppbv and 3–25 ppbv, respectively. The mixing ratios of O3 were highest of 28 ppbv and lowest 19 ppbv during the pre-monsoon and monsoon seasons, respectively. While the mixing ratios of both CO and NOx showed highest and lowest values during the winter and monsoon seasons, respectively. The diurnal pattern of O3 is mainly controlled by the variations in photochemistry and planetary boundary layer (PBL) depth. On the other hand, the seasonality of O3, CO and NOx were governed by the long-range transport associated mainly with the summer and winter monsoon circulations over the Indian subcontinent. The back trajectory data indicate that the seasonal variations in trace gases were caused mainly by the shift in long-range transport pattern. In monsoon season, flow of marine air and negligible presence of biomass burning in India resulted in lowest O3, CO and NOx values. The mixing ratios of CO and NOx show tight correlations during winter and pre-monsoon seasons, while poor correlation in the monsoon season. The emission ratio of ?CO/?NOx showed large seasonal variability but values were lower than those measured over the Indo Gangetic Plains (IGP). The mixing ratios of CO and NOx decreased with the increase in wind speed, while O3 tended to increase with the wind speed. Effects of other meteorological parameters in the distributions of trace gases were also noticed.  相似文献   

2.
Continuous measurements of surface ozone (O3), NOx (NO + NO2) and meteorological parameters have been made in Kannur (11.9?°N, 75.4?°E, 5?m asl), India from November 2009 to October 2010. It was observed that O3 and NOx showed distinct diurnal and seasonal variabilities at this site. The annual average diurnal profile of O3 showed a peak of (30.3?±?10.4) ppbv in the late afternoon and a minimum of (3.2?±?0.7) ppbv in the early morning. The maximum value of O3 mixing ratio was observed in winter (44?±?3.1) ppbv and minimum during monsoon (18.46?±?3.5) ppbv. The rate of production of O3 was found to be higher in December (10.1?ppbv/h) and lower in July (1.8?ppbv/h) during the time interval 0800?C1000?h. A correlation coefficient of 0.52 for the relationship between O3 and [NO2]/[NO] reveals the role of NO2 photolysis that generates O3 at this site. The correlation between O3 and meteorological parameters indicate the influence of seasonal changes on O3 production. Investigations were further extended to explore the week day weekend variations in O3 mixing ratio at an urban site reveals the enhancement of O3. The variations of O3 mixing ratio with seasonal air mass flows were elucidated with the aid of backward air trajectories. This study also indicates how vapor phase organic species present in the ambient air at this location may influence the complex chemistry involving (VOCs) that enhances the production of O3 at this location.  相似文献   

3.
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.  相似文献   

4.
Abstract?This paper presents the results of measurements of the concentration of surface ozone and concurrent standard meteorological parameters: total solar radiation, temperature, relative humidity, pressure, wind speed, and vertical and horizontal components of the wind. The data were collected from 2005 to 2010 at stations located in central Poland (Mazowieckie voivodeship): Warszawa (urban), Legionowo (suburban), Granica and Belsk (rural). Furthermore, Granica is situated in the forested area of Kampinoski National Park. Continuously measured surface ozone concentrations demonstrated the well-known diurnal cycle of surface ozone concentration with a maximum in the afternoon and a minimum in the early morning hours. The averaged diurnal variations over six years reveal that the highest concentrations appear at rural stations (Belsk: 55?µg?m?3 and Granica: 50?µg?m?3) and the lowest at the urban station (Warszawa: 41?µg?m?3). The threshold for high levels of surface ozone (120?µg?m?3 per 8?h) was exceeded most often at Granica and Belsk. The occurrence of the ozone “weekend effect,” especially at urban stations, has been identified. The difference between weekend and weekday surface ozone concentrations at urban and rural stations was as high as 6.5?µg?m?3 and approximately 2?µg?m?3, respectively. Using appropriate statistical tools, it has been shown that meteorological conditions have a significant influence on ozone concentration. High correlation coefficients were found between ozone concentration and solar radiation, temperature, relative humidity, and wind speed. The forward stepwise regression model explains up to 75% of the variations in daily surface ozone concentration in terms of meteorological variability in summer and up to 70% in winter. At the same time, a multilayer perceptron neural network model was used to reconstruct the concentration of surface ozone. High correlation coefficients (up to 0.89) indicate that, on the basis of standard meteorological parameters and NO2 concentration, we can determine ozone concentration with high accuracy.  相似文献   

5.
The mixing ratios of surface O3 were measured at St. John's College, Agra, an urban and traffic influenced area for the period of 2000–2002. The monthly averaged O3 mixing ratios ranged between 8 to 40 ppb with an annual average of 21 ppb. Strong diurnal and seasonal variations in O3 mixing ratios were observed throughout the year except for monsoon season. The mixing ratios of O3 follow the surface temperature cycle and solar radiation (r = 0.72 and r = 0.65 with temperature and solar radiation, respectively). Concentrations were higher with winds associated with NE and NW direction indicating the impact of pollution sources on surface O3 concentration. Exceedance of ozone critical level was calculated using the AOT 40 index and found to be 840 ppb.h and 2430 ppb.h for summer and winter seasons, respectively. The present O3 exposures are lower than the critical level of O3 and suggest that the present level of O3 does not have any impact on reduction in crop yields.  相似文献   

6.
Continuous measurements of ozone and its precursors including NO, NO2, and CO at an urban site (32°03′N, 118°44′E) in Nanjing, China during the period from January 2000 to February 2003 are presented. The effects of local meteorological conditions and distant transports associated with seasonal changed Asian monsoons on the temporal variations of O3 and its precursors are studied by statistical, backward trajectory, and episode analyses. The diurnal variation in O3 shows high concentrations during daytime and low concentrations during late night and early morning, while the precursors show high concentrations during night and early morning and low concentrations during daytime. The diurnal variations in air pollutants are closely related to those in local meteorological conditions. Both temperature and wind speed have significant positive correlations with O3 and significant negative correlations with the precursors. Relative humidity has a significant negative correlation with O3 and significant positive correlations with the precursors. The seasonal variation in O3 shows low concentrations in late autumn and winter and high concentrations in late spring and early summer, while the precursors show high concentrations in late autumn and winter and low concentrations in summer. Local mobile and stationary sources make a great contribution to the precursors, but distant transports also play a very important role in the seasonal variations of the air pollutants. The distant transport associated with the southeastern maritime monsoon contributes substantially to the O3 because the originally clean maritime air mass is polluted when passing over the highly industrialized and urbanized areas in the Yangtze River Delta. The high frequency of this type of air mass in summer causes the fact that a common seasonal characteristic of surface O3 in East Asia, summer minimum, is not observed at this site. The distant transports associated with the northern continental monsoons that dominate in autumn and winter are related to the high concentrations of the precursors in these two seasons. This study can contribute to a better understanding of the O3 pollution in vast inland of China affected by meteorological conditions and the rapid urbanization and industrialization.  相似文献   

7.
The seasonal and diurnal variations of ozone mixing ratios have been observed at Niwot Ridge. Colorado. The ozone mixing ratios have been correlated with the NO x (NO+NO2) mixing ratios measured concurrently at the site. The seasonal and diurnal variations in O3 can be reasonably well understood by considering photochemistry and transport. In the winter there is no apparent systematic diurnal variation in the O3 mixing ratio because there is little diurnal change of transport and a slow photochemistry. In the summer, the O3 levels at the site are suppressed at night due to the presence of a nocturnal inversion layer that isolated ozone near the surface, where it is destroyed. Ozone is observed to increase in the summer during the day. The increases in ozone correlate with increasing NO x levels, as well as with the levels of other compounds of anthropogenic origin. We interpret this correlation as in-situ or in-transit photochemical production of ozone from these precursors that are transported to our site. The levels of ozone recorded approach 100 ppbv at NO x mixing ratios of approximately 3 ppbv. Calculations made using a simple clean tropospheric chemical model are consistent with the NO x -related trend observed for the daytime ozone mixing ratio. However, the chemistry, which does not include nonmethane hydrocarbon photochemistry, underestimates the observed O3 production.  相似文献   

8.
During the summer (8 June through 3 September) of 2008, 9 ozone profiles are examined from Dakar, Senegal (14.75°N, 17.49°W) to investigate ozone (O3) variability in the lower/middle troposphere during the pre-monsoon and monsoon periods. Results during June 2008 (pre-monsoon period) show a reduction in O3 concentrations, especially in the 850–700 hPa layer with Saharan Air Layer (SAL) events. However, O3 concentrations are increased in the 950–900 hPa layer where the peak of the inversion is found and presumably the highest dust concentrations. We also use the WRF-CHEM model to gain greater insights for observations of reduced O3 concentrations during the monsoon periods. In the transition period between 26 June and 2 July in the lower troposphere (925–600 hPa), a significant increase in O3 concentrations (10–20 ppb) occur which we suggest is caused by enhanced biogenic NOX emissions from Sahelian soils following rain events on 28 June and 1 July. The results suggest that during the pre-monsoon period ozone concentrations in the lower troposphere are controlled by the SAL, reducing ozone concentrations through heterogeneous chemical processes. At the base of the SAL we also find elevated levels of ozone, which we attribute to biogenic sources of NOX from Saharan dust that are released in the presence of moist conditions. Once the monsoon period commences, lower ozone concentrations are observed and modeled which we attribute to the dry deposition of ozone and episodes of ozone poor air that is horizontally transported into the Sahel from low latitudes by African Easterly Waves (AEWs).  相似文献   

9.
Surface O3 concentration and its precursors have been observed at Longfengshan station,Heilongjiang Province for a period of one year from August 13,1994 to July 30,1995. Relationship between surface O3 and the meteorological conditions during this period is analyzed in this study.Observation results show that diurnal variation of surface O3 follows a pattern of double-peaks with amplitude of 27-28 ppb under fine days in summer and autumn.Although the diurnal variation is small(14 ppb),it is still detectable when it is overcast.Diurnal variation of O3 is irregular under rainy days.Surface O3 concentration rises when wind speed starts to increase at 0800 BT(Beijing Time)from 0 to 6 m s-1in autumn,winter and summer.Relative high surface O3 concentration is noticed frequently when S,SSW,SW and WSW wind are encountered at the station during all seasons.At 0800 BT and 1400 BT the surface O3 concentration increases with the increase of global radiation accordingly during fine days in winter,spring and autumn.During fine days average peak of O3 concentration in summer is 20 ppb higher than that in winter while the average peak of global radiation in summer is almost twice as high as that in winter.The average surface O3 concentration under fine days in autumn at Longfengshan station is 14 ppb lower in comparison to the observation results from Lin'an station where Lin'an is at about the same longitude and lower latitude,with same environment,which is mainly caused by the difference of global radiation due to different latitudes in these two areas(difference of average peak global radiation about 100 W m-2).  相似文献   

10.
Surface ozone is mainly produced by the photodissociation of nitrogen dioxide (NO2) by solar UV radiation. Subsequently, solar eclipses provide one of the unique occasions to explore the variations in the photolysis rate of NO2 and their significant impact on the production of ozone at a location. This study aims to examine the diurnal variations in the photodissociation rate coefficient of NO2, (j(NO2*)), and mixing ratios of surface ozone and NO X * (NO?+?NO2*) during the solar eclipse that occurred on 15 January 2010 at Kannur (11.9°N, 75.4°E, 5?m amsl), a tropical coastal site on the Arabian Sea in South India. This investigation was carried out on the basis of the ground level observations of surface ozone and its prominent precursor NO2*. The j(NO2*) values were estimated from the observed solar UV-A flux data. A sharp decline in j(NO2*) and surface ozone was observed during the eclipse phase because of the decreased efficiency of the ozone formation from NO2. The NO2* levels were found to increase during this episode, whereas the NO levels remained unchanged. The surface ozone concentration was reduced by 57.5%, whereas, on the other hand, that of NO X * increased by 62.5% during the solar eclipse. Subsequently a reduction of *% in the magnitude of j(NO2*) was found here during the maximum obscuration. Reductions in solar insolation, air temperature and wind speed were also observed during the solar eclipse event. The relative humidity showed a 6.4% decrease during the eclipse phase, which was a unique observation at this site.  相似文献   

11.
China experienced worsening ground-level ozone(O2) pollution from 2013 to 2019. In this study, meteorological parameters, including surface temperature(T2), solar radiation(SW), and wind speed(WS), were classified into two aspects,(1) Photochemical Reaction Condition(PRC = T2× SW) and(2) Physical Dispersion Capacity(PDC = WS). In this way, a Meteorology Synthetic Index(MSI = PRC/PDC) was developed for the quantification of meteorology-induced ground-level O2pollution. The positive linear relationship between the 90 th percentile of MDA8(maximum daily 8-h average) O2concentration and MSI determined that the contribution of meteorological changes to ground-level O-3 varied on a latitudinal gradient, decreasing from ~40% in southern China to 10%–20% in northern China. Favorable photochemical reaction conditions were more important for ground-level O2pollution. This study proposes a universally applicable index for fast diagnosis of meteorological roles in ground-level O2variability, which enables the assessment of the observed effects of precursor emissions reductions that can be used for designing future control policies.  相似文献   

12.
龙凤山大气近地层O3浓度变化及与其它因素的关系   总被引：16，自引：0，他引：16  
研究首次在龙凤山区域大气本底站测得的地面Ｏ３浓度及其变化的资料表明,中国东北农村地面大气Ｏ３浓度总体水平不很高,但在少数特殊的天气条件下,时均浓度可超过国家二级标准。Ｏ３浓度存在明显的季节和日变化,其月平均浓度１９９５年１月最低（２７．５ｐｐｂ）,１９９４年１１月最高（４３．２ｐｐｂ）。Ｏ３日变化幅度夏季的晴天最大（２８ｐｐｂ）,冬季的阴天最小（８ｐｐｂ）。气象要素（尤其是风速、气温和相对湿度等）和ＮＯｘ与地面Ｏ３浓度有较密切的关系。用多变量分析法探讨了地面Ｏ３各指标随气象因子和ＮＯｘ共同变化的规律,并拟合了寒冷和温暖期里与地面Ｏ３日最高浓度、日最低浓度及日变化幅度有关的方程。  相似文献   

13.
The explosive spread of the 2019 novel coronavirus (COVID-19) provides a unique chance to rethink the relationship between human activity and air pollution. Though related studies have revealed substantial reductions in primary emissions, obvious differences do exist in the responses of secondary pollutants, like ozone (O3) pollution. However, the regional disparities of O3 responses and their causes have still not been fully investigated. To better elucidate the interrelationship between anthropogenic emissions, chemical production, and meteorological conditions, O3 responses caused by lockdowns over different regions were comprehensively explored at a global scale. Observational signals of air-quality change were derived from multi-year surface measurements and satellite retrievals. With similar substantial drops in nitrogen dioxide (NO2), ozone shows rising signals in most areas of both East Asia and Europe, even up to ∼14 ppb, while a non-negligible declining signal exists in North America, by about 2–4 ppb. Furthermore, the drivers behind the different O3 responses are discussed based on meteorological analysis and O3 sensitivity diagnosis. On the one hand, O3 responses to NO2 declines can be affected by the primary dependence on its precursors. On the other hand, it is also highly dependent on meteorological factors, especially temperature. Our study further highlights the great importance of taking into consideration both the regional disparities and synergistic effects of precursor reductions and meteorological influence for scientific mitigation of O3 pollution.摘要疫情期间全球各地一次排放大幅削减, 而臭氧等二次污染的响应则存在着区域间差异.结合地面和卫星观测发现, 同在氮氧化物大幅下降的情况下,臭氧在东亚和欧洲呈现出可达14ppb的上升信号, 而北美则下降为主 (约2–4ppb) .我们结合气象分析和臭氧敏感性进一步讨论了臭氧响应差异性的原因, 一方面受臭氧与前体物间关系的影响;另一方面来自于气象, 尤其是温度.研究明晰了人为排放,化学和气象三者的内在关联, 强调了在臭氧控制过程中考虑前体物削减和气象条件协同的重要性.  相似文献   

14.
In order to study the concentrations of hydrogen peroxide (H2O2) and the factors controlling its concentrations, we monitored concentrations of H2O2 and other gases such as sulfur dioxide, ozone, and NO x as well as meteorological factors such as air temperature, relative humidity, and wind direction/speed during eight measurement periods from 2000 to 2002 in a Japanese red pine forest in Japan. The H2O2 concentrations ranged from below 0.01 to 1.64 ppb, and analysis of the diurnal variation in H2O2 concentration showed high concentrations around noon, and low concentrations in the morning and late afternoon. The H2O2 concentrations were high in early summer, when O3 concentration, temperature, and solar radiation were high, and were low in fall, when O3 concentration, temperature, and solar radiation were low. We propose that O3 concentration affects the production of H2O2 in the monitored region during the period under study, but that high H2O2 concentrations were sometimes caused by the transport of polluted air from urban regions. H2O2 concentrations decreased remarkably when SO2 concentrations increased by transported volcanic emission on Miyake Island. In the absence of the effects of SO2, H2O2 concentrations increased with increasing O3 concentration and temperature.  相似文献   

15.
利用2017~2018年阿克达拉逐时臭氧浓度监测数据和同期气象观测资料,分析了阿克达拉近地面臭氧浓度的日変化和年季变化特征,并分析了臭氧浓度与气象条件之间的关系。结果表明：臭氧浓度日变化呈现单峰型,下午16点前后达到最高值,最高值分别为42.86 ppb和38.37 ppb；2017和2018年阿克达拉臭氧最高月分别出现在3月和2月,月平均臭氧浓度为49.37 ppb和37.94 ppb,最低月出现在12月,浓度为18.36 ppb和18.90 ppb；2017~2018年阿克达拉近地面臭氧浓度的季节变化规律为：春季＞夏季＞冬季＞秋季；阿克达拉的主导风向是NW和E,夏季主导风向为NW,冬季则以偏东风为主；夏季受西北气流影响,阿克达拉西北方向的污染源对当地近地面臭氧浓度影响较大。  相似文献   

16.
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 Ox(= 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.  相似文献   

17.
对临安大气本底站2003-2004年冬、夏季二氧化氮(NO2)、二氧化硫(SO2)、臭氧(O3)进行了分析.结果表明:冬季NO2和SO2平均体积分数分别为19.48×10-9和35.74 x10-9,而夏季的平均体积分数分别为4.81×10-9和8.12×10-9,冬季高于夏季;O3在夏季的平均体积分数为33.55×10-9,略高于冬季的25.44×10-9;夜间NO2和SO2体积分数比白天高,并且NO2呈明显的单峰单谷型分布,O3也呈单峰型但峰值出现在白天.NO2、SO2体积分数存在着明显的“假日效应”,假日比非假日低,周五高于假日和非假日;但O3体积分数没有明显的假日效应.降水对SO2有明显的清除作用,但对NO2的清除作用不明显.与风向对比发现,夏季高体积分数的NO2、SO2都受到NW、WNW风的影响,冬季则分别受NE和SW、SSW风的影响;而O3受风向的影响较复杂,与局地光化学反应有关.  相似文献   

18.
Measurements of NOx,y were made at Alert, Nunavut, Canada (82.5° N, 62.3° W) during surface layer ozone depletion events. In spring 1998, depletion events were rare and occurred under variable actinic flux, ice fog, and snowfall conditions. NOy changed by less than 10% between normal, partially depleted, and nearly completely depleted ozone air masses. The observation of a diurnal variation in NOx under continuous sunlight supports a source from the snowpack but with rapid conversion to nitrogen reservoirs that are primarily deposited to the surface or airborne ice crystals. It was unclear whether NOx was reduced or enhanced in different stages of the ozone depletion chemistry because of variations in solar and ambient conditions. Because ozone was depleted from 15–20 ppbv to less than 1 ppbv in just over a day in one event it is apparent that the surface source of NOx did not grossly inhibit the removal of ozone. In another case ozone was shown to be destroyed to less than the 0.5 ppbv detection limit of the instrument. However, simple model calculations show that the rate of depletion of ozone and its final steady-state abundance depend sensitively on the strength of the surface source of NOx due to competition from ozone production involving NOx and peroxy radicals. The behavior of the NO/NO2 ratio was qualitatively consistent with enhanced BrO during the period of active ozone destruction. The model is also used to emphasize that the diurnal partitioning of BrOx during ozone depletion events is sensitive to even sub ppbv variations in O3.  相似文献   

19.
We studied the daily patterns in the rates of terpene emissions by the montane holm oak, Quercus ilex, in three typical days of winter and three typical days of summer in Montseny, a natural park near Barcelona, and related them to the air concentrations of terpenes, ozone and NO2. Terpene emission rates were about 10 times higher in summer than in winter. Emissions virtually stopped in the dark. In both seasons, rates of terpene emissions were well correlated with light, air temperature and relative humidity. Rates of emissions were also correlated with stomatal conductance and the rates of transpiration and photosynthesis. Almost all the individual terpenes identified followed the same pattern as total terpenes. The most abundant terpene was ??-pinene, followed by sabinene + ??-pinene, limonene, myrcene, camphene and ??-phellandrene. Atmospheric terpene concentrations were also about 10 times higher in summer than in winter. A significant diurnal pattern with maxima at midday was observed, especially in summer. The increase by one order of magnitude in the concentrations of these volatile isoprenoids highlights the importance of local biogenic summer emissions in these Mediterranean forested areas which also receive polluted air masses from nearby or distant anthropic sources. Atmospheric concentrations of O3 and NO2 were also significantly higher in summer and at midday hours. In both seasons, concentrations of O3 were significantly correlated with concentrations of terpenes and NO2 in the air and with rates of terpene emission.  相似文献   

20.
Simultaneous observations of surface ozone (O3) with its precursors namely, carbon monoxide (CO) and oxides of nitrogen (NOx) have been taken on diurnal scale from a tropical semi-urban site, Pune (18.54°N, 73.81°E) in India. We present the data for one year (2003–2004) period to study the salient features of these trace gases. The peak in amplitude of ozone is found during the noontime whereas in CO and NOX it is observed in the morning hours between 0800 and 0900 H. The concentration of these pollutants drop down considerably during southwest monsoon months and the diurnal pattern also become very weak. The diurnal trends of these gases are found to be different for different seasons, which are specific to the receptor site. Model simulations using 3-D chemical-transport model with regional emission inventories and observed winds have also been carried out. The comparison of model results with observations, on seasonal basis yielded a reasonable qualitative agreement. The relative role of local emissions and long range transport in the diurnal pattern for different seasons has been outlined, which reveals that the ozone is highly influenced by regional/long range transport in this region. The effect of precursor amounts in the morning on afternoon ozone peak levels has been investigated using the lag correlation study, which reveals that a time lag of 5–7 h is required for most of these precursor gases to photo-chemically produce ozone to its maximum potential. Results are discussed in the light of available topographic and meteorological conditions.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号