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1.
利用2013-2019年银川市主要污染物浓度数据,分析了近年来银川市主要污染物浓度变化特征,并运用主成分分析法对主要污染物之间的关系进行研究。结果表明：近年来银川市主要污染物浓度除O3逐年呈上升趋势外,其他均呈下降趋势;市区站O3浓度较郊区背景站低,其他污染物市区较郊区背景站高;市区站PM10和PM2.5浓度超国家二级标准;除O3浓度夏季高,冬季低外,其他污染物冬季高,夏季低;CO、NO2、PM10、PM2.5浓度呈"双峰型"日变化特征,O3和SO2呈"单峰型"日变化特征。银川市主要污染物NO2浓度与CO和O3相关性显著,PM10和PM2.5之间相关性显著;污染物第一主成分是NO2、CO和O3,方差贡献率达到50%以上,加之银川市O3浓度逐年呈升高趋势,表明近年来银川市大气光化学污染增加。 相似文献
2.
为了进一步了解青藏高原闪电的产生氮氧化物（LNOx）经由光化学反应对O3浓度变化及夏季O3低谷形成的可能影响,本文利用2005~2013年由OMI卫星得到的对流层NO2垂直浓度柱（NO2 VCD）、O3总浓度柱（TOC）和O3廓线以及星载光学瞬变探测器OTD和闪电成像仪LIS获取的总闪电数资料,对青藏高原和同纬度长江中下游地区的TOC和NO2 VCD月均值时空分布特征、闪电与NO2 VCD的相关性和O3的垂直分布特征及其与LNOx的关系进行了对比分析。结果表明,青藏高原的O3低谷主要出现在夏季和秋季,其TOC值比同纬度长江中下游地区低约10~15 DU（Dobson unit）。青藏高原NO2VCD总体较小,表现为夏高冬低的分布特征。青藏高原夏季O3浓度受南亚高压的影响总体呈减小趋势,但因强雷暴天气导致对流层中上部LNOx浓度升高,并随强上升气流向对流层顶输送,同时通过光化学反应使O3浓度增加,缩小了青藏高原和同纬度地区的O3浓度差,减缓了O3总浓度的下降,抑制了夏季O3低谷的进一步深化。 相似文献
3.
利用成都市城区2015年12月~2019年12月污染物浓度及气象资料,对PM10、PM2.5、CO、O3、 SO2、NO2六种大气污染物浓度变化特征以及与气象要素之间的相关性进行分析。结果表明:2016~2019年成都市空气质量冬季最差,秋季最好,年内整体以良为主,重度污染和严重污染的天气较少出现,空气质量逐年变好;主要污染物浓度除O3外在冬季最高,夏季最低,春秋两季相差不大,O3浓度变化则相反;主要污染物的日变化特征也较为明显。空气质量综合指数、PM10、PM2.5、CO、NO2浓度与气温和降水存在显著负相关性,与气压存在显著正相关性,还与相对湿度呈不同程度的负相关,但与风速相关性不显著;O3浓度不仅与风速、气温和降水存在显著的正相关,还与气压呈显著的负相关,却与相对湿度的负相关性不显著。 相似文献
4.
为了揭示我国北方地区对流层中下层臭氧(O3) 的形成机理以及周边地区的污染输送对我国北方地区对流层中下层O3收支的影响, 在与外场观测数据比较分析的基础上, 利用全球化学输送模式(MOZART-2) 采用收支分析方法定量分析了影响我国北方地区对流层中下层O3的各个物理化学过程。结果表明:我国北方地区对流层下层O3最重要的来源是光化学生成作用, 约占总来源的58.3%(41.5 Tg), 光化学生成反应中HO2对于O3生成的贡献最大; 最大的汇是干沉降过程, 约占总汇的43.2%(26.2Tg); 水平净输送作用对我国北方地区对流层中下层O3收支的影响非常大, 在我国北方地区对流层下层, 41.6%左右的O3来自水平净输送, 随高度增加, 水平输送影响增大, 我国北方地区对流层中层大约81.5%的O3来自水平净输送。 相似文献
5.
利用2015—2019年辽宁城市逐小时地面O3浓度观测数据,结合各城市逐小时气象要素观测数据,分析了辽宁地区近5 a的O3污染状况及影响O3的相关气象条件。结果表明：除环辽东湾部分城市O3浓度呈下降趋势外,辽宁地区其他城市的O3浓度均呈明显的上升趋势,O3正取代PM2.5成为影响辽宁地区的首要大气污染物。O3浓度具有夏季高、冬季低,下午高、早晨低的时间分布特征。除受污染排放源直接影响外,高温、高湿、强辐射、小风和地面低气压都有利于O3的局地生成;在亚洲夏季风的影响下,上游地区（如京津冀地区）的污染气团会随大气环流向东北地区输送,对辽宁地区夏季O3污染产生重要影响。 相似文献
6.
利用2017—2019年夏季（6—8月）太原市污染物浓度和气象逐小时数据,分析了太原南部城区O3浓度及其影响因子的变化特征,通过神经网络构建了O3与其影响因子的关系模型,并进行了检验。结果表明：2017—2019年夏季太原南部城区O3浓度超标天数分别为55 d、39 d、59 d,超标主要集中在6月和7月;O3浓度日变化特征呈单峰型,每日06时前后达到最低,15时前后达到峰值。高温、强辐射、低湿、低压、西南风容易引起太原南部城区O3浓度升高,西北风有利于O3扩散;NO2、CO与O3浓度表现为负相关关系,但NO2对其影响更加显著。利用神经网络构建O3浓度与影响因子的关系模型,相关系数达0.96,均方根误差、平均绝对误差分别为8 μg·m-3、6%,TS评分为0.95,神经网络模型具有较高预报能力,可为太原地区O3预报提供参考价值。 相似文献
7.
8.
本文利用2017年彭州市大气污染物(SO2、NO2、O3、CO、PM10、PM2.5)小时浓度数据并结合地面气象观测资料,统计分析了该地区大气污染物浓度的演变规律及影响因素。结果表明:该地区细粒子(PM10和PM2.5)污染较为严重,O3次之,其它污染物浓度水平则低于国家新二级标准限值。观测期间,各污染物浓度表现出明显的日变化与季节变化,其中SO2、O3呈单峰型日变化,NO2、CO和细粒子则呈双峰型日变化;污染物浓度的季节变化基本表现为冬高夏低、春秋次之的变化特征(O3为夏高冬低),并且固态污染物(PM10、PM2.5)与气态污染物(NO2、CO)之间有显著的相关性。在污染物浓度与气象要素相关性分析中表明,湿度对于污染物浓度的影响整体上要弱于温度和风速,除了O3与温度、风速呈正相关外,其它污染物与两者均呈负相关。除此以外,风向对于当地各种大气污染物的积累与清除也有直接的影响。 相似文献
9.
2013年6—9月在河北省固城站观测到多次夜间对流性天气伴随地面O3混合比快速抬升的过程,并引起次日清晨到中午O3混合比升高。大多数对流过程中,O3混合比在半小时内升高至60×10-9～80×10-9,同时NOx等反应性气体混合比下降,θse值降低,说明下沉气流将高空气团带到地面,造成了O3混合比的升高。通过再分析资料得到下沉气团基本来源于对流层中下层,这一结论与当地进行的一次飞机观测结果吻合。多数对流过程中固城站和北京城区地面O3混合比和θse值有相同的变化趋势和程度。根据观测结果,推测华北地区在夏季和初秋时,对流层中下层存在O3高值区,混合比约为60×10-9～80×10-9。对流性天气对地面O3抬升的影响区域与对流系统的影响范围有关,可达到中尺度范围。华北地区光化学污染严重,对流性天气引起的地面O3混合比抬升程度比较强,对环境的影响值得关注。 相似文献
10.
基于上海地区2012—2016年逐日PM2.5、PM10、CO、O3、SO2、NO2的分指数（individual air quality index,IAQI）数据以及同期气象要素（风速、降水量、气温、相对湿度、总云量、低云量）、逆温数据和高空大气环流数据,分析了上海地区空气质量指数的时间变化特征和气候要素对空气质量的影响,并选取PM2.5和O3污染天气过程及其邻近的非污染天气过程,对比分析高空大气环流形势的差异。结果表明：上海地区出现PM2.5、PM10和NO2污染天气在冬季最多,分别为31.4 d、10.0 d和14.8 d,而O3污染天气在夏季最多（18.8 d）。风速和低云量是影响PM2.5污染的重要气象因素,最大相关系数分别为-0.313和-0.261,O3污染则与气温和日照时数密切相关,最大相关系数分别为0.449和0.363,PM2.5、O3污染的发生也与前一日以及当日出现逆等温天气存在较好的相关性。在PM2.5污染天气过程,上海位于槽后高压前部,850 hPa有较强西北风,而非PM2.5污染天气过程中上海位于高压后部,低层850 hPa为东南风。在O3污染天气和非污染天气过程,中国东部长波射出辐射（Outgoing Longwave Radiation,OLR）分别为正、负距平,副热带高压控制下上海晴热少云,易引起O3污染,反之上海上空云系多,不容易出现污染。 相似文献
11.
G. Salisbury P. S. Monks S. Bauguitte B. J. Bandy S. A. Penkett 《Journal of Atmospheric Chemistry》2002,41(2):163-187
Measurements of the sum of peroxy radicals [HO2 + RO2],NOx (NO + NO2) and NOy (the sum of oxidisednitrogen species) made at Mace Head, on the Atlantic coast of Ireland in summer 1996 and spring 1997 are presented. Together with a suite of ancillary measurements, including the photolysis frequencies of O3 O(1D)(j(O1D)) and NO2 (j(NO2)), the measured peroxy radicals are used to calculate meandailyozone tendency (defined as the difference of the in-situphotochemical ozone production and loss rates); these values are compared with values derived from the photochemical stationary state (PSS) expression. Although the correlation between the two sets of values is good, the PSS values are found to be significantly larger than those derived from the peroxy radical measurements, on average, in line with previous published work. Possible sources of error in these calculations are discussed in detail. The data are further divided up into five wind sectors, according to the instantaneous wind direction measured at the research station. Calculation of mean ozone tendencies by wind sector shows that ozone productivity was higher during spring (April–May) 1997 than during summer (July–August) 1996across all airmasses, suggesting that tropospheric photochemistry plays an important role in the widely-reported spring ozone maximum in the Northern Hemisphere. Ozone tendencies were close to zero for the relatively unpolluted south-west, west and north-west wind sectors in the summer campaign, whereas ozone productivity was greatest in the polluted south-east sector for both campaigns. Daytime weighted average ozone tendencies were +(0.3± 0.1) ppbv h–1 for summer 1996 and +(1.0± 0.5) ppbvh–1 for spring 1997. These figures reflect the higher mixing ratios of ozone precursors in spring overall, as well as the higher proportion of polluted air masses from the south-east arriving at the site during the spring campaign. The ozone compensation point, where photochemical ozone destruction and production processes are in balance, is calculated to be ca. 14 pptv NO for both campaigns. 相似文献
12.
A NUMERICAL STUDY OF THE VARIATIONS AND DISTRIBUTIONS OF TROPOSPHERIC OZONE AND ITS PRECURSORS OVER CHINA* 
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下载免费PDF全文 By means of a three-dimensional meteorological model (MM5) and a chemical model,the distributions of tropospheric ozone and its precursors over China have been simulated in summer and winter time,16-18 August 1994 and 7-9 January 1995.The distribution of ozone over the Tibetan Plateau in summer time is deeply discussed.The simulated results indicate that thedistributions of surface ozone and NOx are in good agreement with observed results,and human activities and photochemical reactions are the main factors controlling the surface ozone and NOx concentrations.In addition,higher ozone concentrations are coincided with the air convergence,and the lower concentrations are related to the air divergence.In summer,over the Tibetan Plateau the strong flow convergence results in higher ozone concentrations in the lower troposphere:and the strong flow divergence results in lower ozone concentrations in the upper troposphere.In winter time ozone concentrations show large-scale characteristics controlled by westerly flow,and in the jet area they are lower than those outside the jet. 相似文献
13.
D. D. Parrish D. W. Fahey E. J. Williams S. C. Liu M. Trainer P. C. Murphy D. L. Albritton F. C. Fehsenfeld 《Journal of Atmospheric Chemistry》1986,4(1):63-80
The mixing ratios for ozone and NOx (NO+NO2) have been measured at a rural site in the United States. From the seasonal and diurnal trends in the ozone mixing ratio over a wide range of NOx levels, we have drawn certain conclusions concerning the ozone level expected at this site in the absence of local photochemical production of ozone associated with NOx from anthropogenic sources. In the summer (June 1 to September 1), the daily photochemical production of ozone is found to increase in a linear fashion with increasing NOx mixing ratio. For NOx mixing ratios less than 1 part per billion by volume (ppbv), the daily increase is found to be (17±3) [NOx]. In contrast, the winter data (December 1 to March 1) indicate no significant increase in the afternoon ozone level, suggesting that the photochemical production of ozone during the day in winter approximately balances the chemical titration of ozone by NO and other pollutants in the air. The extrapolated intercept corresponding to [NOx]=0 taken from the summer afternoon data is 13% less than that observed from the summer morning data, suggesting a daytime removal mechanism for O3 in summer that is attributed to the effects of both chemistry and surface deposition. No significant difference is observed in the intercepts inferred from the morning and afternoon data taken during the winter.The results contained herein are used to deduce the background ozone level at the measurement site as a function of season. This background is equated with the natural ozone background during winter. However, the summer data suggest that the background ozone level at our site is elevated relative to expected natural ozone levels during the summer even at low NOx levels. Finally, the monthly daytime ozone mixing ratios are reported for 0[NOx]0.2 ppbv, 0.3 ppbv[NOx]0.7 ppbv and 1 ppbv[NOx]. These monthly ozone averages reflect the seasonal ozone dependence on the NOx level. 相似文献
14.
Kenneth E. Pickering Anne M. Thompson John R. Scala Wei-Kuo Tao Joanne Simpson 《Journal of Atmospheric Chemistry》1992,14(1-4):297-313
The effects of deep convection on the potential for forming ozone (ozone production potential) in the free troposphere have been simulated for regions where the trace gas composition is influenced by biomass burning. Cloud dynamical and photochemical simulations based on observations in 1980 and 1985 Brazilian campaigns form the basis of a sensitivity study of the ozone production potential under differing conditions. The photochemical fate of pollutants actually entrained in a cumulus event of August 1985 during NASA/GTE/ABLE 2A (Case 1) is compared to photochemical ozone production that could have occurred if the same storm had been located closer to regions of savanna burning (Case 2) and forest burning (Case 3). In each case studied, the ozone production potential is calculated for a 24-hour period following convective redistribution of ozone precursors and compared to ozone production in the absence of convection. In all cases there is considerably more ozone formed in the middle and upper troposphere when convection has redistributed NOx, hydrocarbons and CO compared to the case of no convection.In the August 1985 ABLE 2A event, entrainment of a layer polluted with biomass burning into a convective squall line changes the free tropospheric cloud outflow column (5–13 km) ozone production potential from net destruction to net production. If it is assumed that the same cloud dynamics occur directly over regions of savanna burning, ozone production rates in the middle and upper troposphere are much greater. Diurnally averaged ozone production following convection may reach 7 ppbv/day averaged over the layer from 5–13 km-compared to typical free tropospheric concentrations of 25–30 ppbv O3 during nonpolluted conditions in ABLE 2A. Convection over a forested region where isoprene as well as hydrocarbons from combustion can be transported into the free troposphere leads to yet higher amounts of ozone production. 相似文献
15.
Michael Keller Daniel J. Jacob Steven C. Wofsy Robert C. Harriss 《Climatic change》1991,19(1-2):139-158
A major portion of tropospheric photochemistry occurs in the tropics. Deforestation, colonization, and development of tropical rain forest areas could provoke significant changes in emissions of radiatively and photochemically active trace gases. A brief review of studies on trace-gas emissions in pristine and disturbed tropical habitats is followed by an effort to model regional tropospheric chemistry under undisturbed and polluted conditions. Model results suggest that changing emissions could stimulate photochemistry leading to enhanced ozone production and greater mineral acidity in rainfall in colonized agricultural regions. Model results agree with measurements made during the NASA ABLE missions. Under agricultural/pastoral development scenarios, tropical rain forest regions could export greater levels of N2O, CH4, CO, and photochemical precursors of NO
y
and O3 to the global atmosphere with implications for climatic warming. 相似文献
16.
The global three-dimensional Lagrangian chemistry-transport model STOCHEM has been used to follow the changes in the tropospheric distributions of the two major radiatively-active trace gases, methane and tropospheric ozone, following the emission of pulses of the short-lived tropospheric ozone precursor species, methane, carbon monoxide, NOx and hydrogen. The radiative impacts of NOx emissionswere dependent on the location chosen for the emission pulse, whether at the surface or in the upper troposphere or whether in the northern or southern hemispheres. Global warming potentials were derived for each of the short-lived tropospheric ozone precursor species by integrating the methane and tropospheric ozone responses over a 100 year time horizon. Indirect radiative forcing due to methane and tropospheric ozone changes appear to be significant for all of the tropospheric ozone precursor species studied. Whereas the radiative forcing from methane changes is likely to be dominated by methane emissions, that from tropospheric ozone changes is controlled by all the tropospheric ozone precursor gases, particularly NOxemissions. The indirect radiative forcing impacts of tropospheric ozone changes may be large enough such that ozone precursors should be considered in the basket of trace gases through which policy-makers aim to combat global climate change. 相似文献
17.
Y. Kondo H. Muramatsu W. A. Matthews N. Toriyama M. Hirota 《Journal of Atmospheric Chemistry》1988,6(3):235-250
In summer, atmospheric ozone was measured from an aircraft platform simultaneously with nitric oxide (NO), oxides of nitrogen (NO
y
), and water vapor over the Pacific Ocean in east Asia from 34° N to 19° N along the longitude of 138±3°E. NO
y
was measured with the aid of a ferrous sulfate converter. The altitude covered was from 0.5 to 5 km. A good correlation in the smoothed meridional distributions between ozone and NO
y
was seen. In particular, north of 25° N, ozone and NO
y
mixing ratios were considerably higher than those observed in tropical marine air south of 25° N. NO
y
and O3 reached a minimum of 50 pptv and 4 ppbv respectively in the boundary layer at a latitude of 20° N. The NO concentration between 2 and 5 km at the same latitude was 30 pptv. The profiles of ozone and water vapor mixing ratios were highly anti-correlated between 25° N and 20° N. In contrast, it was much poorer at the latitude of 33° N, suggesting a net photochemical production of ozone there. 相似文献
18.
F. C. Fehsenfeld M. J. Bollinger S. C. Liu D. D. Parrish M. McFarland M. Trainer D. Kley P. C. Murphy D. L. Albritton D. H. Lenschow 《Journal of Atmospheric Chemistry》1983,1(1):87-105
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
19.
Shu Li Tijian Wang Prodromos Zanis Dimitris Melas Bingliang Zhuang 《Acta Meteorologica Sinica》2018,32(2):279-287
The spatial distribution, radiative forcing, and climatic effects of tropospheric ozone in China during summer were investigated by using the regional climate model RegCM4. The results revealed that the tropospheric ozone column concentration was high in East China, Central China, North China, and the Sichuan basin during summer. The increase in tropospheric ozone levels since the industrialization era produced clear-sky shortwave and clear-sky longwave radiative forcing of 0.18 and 0.71 W m–2, respectively, which increased the average surface air temperature by 0.06 K and the average precipitation by 0.22 mm day–1 over eastern China during summer. In addition, tropospheric ozone increased the land–sea thermal contrast, leading to an enhancement of East Asian summer monsoon circulation over southern China and a weakening over northern China. The notable increase in surface air temperature in northwestern China, East China, and North China could be attributed to the absorption of longwave radiation by ozone, negative cloud amount anomaly, and corresponding positive shortwave radiation anomaly. There was a substantial increase in precipitation in the middle and lower reaches of the Yangtze River. It was related to the enhanced upward motion and the increased water vapor brought by strengthened southerly winds in the lower troposphere. 相似文献
20.
The response of tropospheric ozone to a change in solar UV penetration due to perturbation on column ozone depends critically on the tropospheric NO
x
(NO+NO2) concentration. At high NO
x
or a polluted area where there is net ozone production, a decrease in column ozone will increase the solar UV penetration to the troposphere and thus increase the tropospheric ozone concentration. However, the opposite will occur, for example, at a remote oceanic area where NO
x
is so low that there is net ozone destruction. This finding may have important implication on the interpretation of the long term trend of tropospheric ozone. A change in column ozone will also induce change in tropospheric OH, HO2, and H2O2 concentrations which are major oxidants in the troposphere. Thus, the oxidation capacity and, in turn, the abundances of many reduced gases will be perturbed. Our model calculations show that the change in OH, HO2, and H2O2 concentrations are essentially independent of the NO
x
concentration. 相似文献