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1.
Source identification of PM2.5 particles measured in Gwangju, Korea   总被引:1,自引:0,他引:1  
The UNMIX and Chemical Mass Balance (CMB) receptor models were used to investigate sources of PM2.5 aerosols measured between March 2001 and February 2002 in Gwangju, Korea. Measurements of PM2.5 particles were used for the analysis of carbonaceous species (organic (OC) and elemental carbon (EC)) using the thermal manganese dioxide oxidation (TMO) method, the investigation of seven ionic species using ion chromatography (IC), and the analysis of twenty-four metal species using Inductively Coupled Plasma (ICP)-Atomic Emission Spectrometry (AES)/ICP-Mass Spectrometry (MS). According to annual average PM2.5 source apportionment results obtained from CMB calculations, diesel vehicle exhaust was the major contributor, accounting for 33.4% of the measured PM2.5 mass (21.5 μg m− 3), followed by secondary sulfate (14.6%), meat cooking (11.7%), secondary organic carbon (8.9%), secondary nitrate (7.6%), urban dust (5.5%), Asian dust (4.4%), biomass burning (2.8%), sea salt (2.7%), residual oil combustion (2.6%), gasoline vehicle exhaust (1.9%), automobile lead (0.5%), and components of unknown sources (3.4%). Seven PM2.5 sources including diesel vehicles (29.6%), secondary sulfate (17.4%), biomass burning (14.7%), secondary nitrate (12.6%), gasoline vehicles (12.4%), secondary organic carbon (5.8%) and Asian dust (1.9%) were identified from the UNMIX analysis. The annual average source apportionment results from the two models are compared and the reasons for differences are qualitatively discussed for better understanding of PM2.5 sources.Additionally, the impact of air mass pathways on the PM2.5 mass was evaluated using air mass trajectories calculated with the Hybrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) backward trajectory model. Source contributions to PM2.5 collected during the four air mass patterns and two event periods were calculated with the CMB model and analyzed. Results of source apportionment revealed that the contribution of diesel traffic exhaust (47.0%) in stagnant conditions (S) was much higher than the average contribution of diesel vehicle exhaust (33.4%) during the sampling period. During Asian dust (AD) periods when the air mass passed over the Korean peninsula, Asian dust and secondary organic carbon accounted for 25.2 and 23.0% of the PM2.5 mass, respectively, whereas Asian dust contributed only 10.8% to the PM2.5 mass during the AD event when the air mass passed over the Yellow Sea. The contribution of biomass burning to the PM2.5 mass during the biomass burning (BB) event equaled 63.8%.  相似文献   

2.
An extensive aerosol sampling program was conducted during January-December 2006 over Kolkata (22o33?? N and 88o20?? E), a mega-city in eastern India in order to understand the sources, distributions and properties of atmospheric fine mode aerosol (PM2.5). The primary focus of this study is to determine the relative contribution of natural and anthropogenic as well as local and transported components to the total fine mode aerosol loading and their seasonal distributions over the metropolis. The average concentrations of fine mode aerosol was found to be 71.2?±?25.2???gm-3 varying between 34.5???gm-3 in monsoon and 112.6???gm-3 in winter. The formation pathways of major secondary aerosol components like nitrate and sulphate in different seasons are discussed. A long range transport of dust aerosol from arid and semi-arid regions of western India and beyond was observed during pre-monsoon which significantly enriched the total aerosol concentration. Vehicular emissions, biomass burning and transported dust particles were the major sources of PM2.5 from local and continental regions whereas sea-salt aerosol was the major source of PM2.5 from marine source regions.  相似文献   

3.

In this study we present the seasonal chemical characteristics and potential sources of PM10 at an urban location of Delhi, India during 2010?2019. The concentrations of carbonaceous aerosols [organic carbon (OC), elemental carbon (EC), water soluble organic carbon (WSOC) and water insoluble organic carbon (WIOC)] and elements (Al, Fe, Ti, Cu, Zn, Mn, Pb, Cr, F, Cl, Br, P, S, K, As, Na, Mg, Ca, B, Ni, Mo, V, Sr, Zr and Rb) in PM10 were estimated to explore their possible sources. The annual average concentration (2010–2019) of PM10 was computed as 227?±?97 µg m?3 with a range of 34?734 µg m?3. The total carbonaceous aerosols in PM10 was accounted for 22.5% of PM10 mass concentration, whereas elements contribution to PM10 was estimated to be 17% of PM10. The statistical analysis of OC vs. EC and OC vs. WSOC of PM10 reveals their common sources (biomass burning and/or fossil fuel combustion) during all the seasons. Enrichment factors (EFs) of the elements and the relationship of Al with other crustal metals (Fe, Ca, Mg and Ti) of PM10 indicates the abundance of mineral dust over Delhi. Principal component analysis (PCA) extracted the five major sources [industrial emission (IE), biomass burning?+?fossil fuel combustion (BB?+?FFC), soil dust, vehicular emissions (VE) and sodium and magnesium salts (SMS)] of PM10 in Delhi, India. Back trajectory and cluster analysis of airmass parcel indicate that the pollutants approaching to Delhi are mainly from Pakistan, IGP region, Arabian Sea and Bay of Bengal.

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4.
Ambient concentrations of organic carbon (OC), elemental carbon (EC) and water soluble inorganic ionic components (WSIC) of PM10 were studied at Giridih, Jharkhand, a sub-urban site near the Indo Gangatic Plain (IGP) of India during two consecutive winter seasons (November 2011–February 2012 and November 2012–February 2013). The abundance of carbonaceous and water soluble inorganic species of PM10 was recorded at the study site of Giridih. During winter 2011–12, the average concentrations of PM10, OC, EC and WSIC were 180.2?±?46.4; 37.2?±?6.2; 15.2?±?5.4 and 18.0?±?5.1 μg m?3, respectively. Similar concentrations of PM10, OC, EC and WSIC were also recorded during winter 2012–13. In the present case, a positive linear trend is observed between OC and EC at sampling site of Giridih indicates the coal burning, as well as dispersed coal powder and vehicular emissions may be the source of carbonaceous aerosols. The principal components analysis (PCA) also identifies the contribution of coal burning? +?soil dust, vehicular emissions?+?biomass burning and seconday aerosol to PM10 mass concentration at the study site. Backward trajectoy and potential source contributing function (PSCF) analysis indicated that the aerosols being transported to Giridih from upwind IGP (Punjab, Haryana, Uttar Pradesh and Bihar) and surrounding region.  相似文献   

5.
The main objective of this study is to investigate the chemical characteristics of biomass burning aerosol and its impact on regional air quality during an agricultural waste burning period in early summer in the rural areas of Korea. A 12-h integrated intensive sampling of biomass burning aerosol in the fine and coarse modes was conducted on 2–20 June 2003 in Gwangju, Korea. The collected samples were analyzed for concentrations of mass, ionic, elemental, and carbonaceous species. Average concentrations of fine and coarse mass were measured to be 67.9 and 18.7 μg m− 3 during the biomass burning period, 41.9 and 18.8 μg m− 3 during the haze period, and 35.6 and 13.3 μg m− 3 during the normal period, respectively. An exceptionally high PM2.5 concentration of 110.3 μg m− 3 with a PM2.5/PM10 ratio of 0.79 was observed on 6 June 2003 during the biomass burning period. The potassium ratio method was used to identify biomass burning samples. The average ratio of potassium in the fine mode to the coarse mode (FK/CK) was 23.8 during the biomass burning period, 6.0 during the haze period, and 4.7 during the normal period, respectively. A FK/CK ratio above 9.2 was considered a criterion for biomass burning event in this study. Particulate matter from the open field burning of agricultural waste has an adverse impact on visibility, human health, and regional air quality.  相似文献   

6.
Concentrations of thirty-five trace elements in ambient fine particulate matter (PM2.5) were measured from September 2001 to January 2002 in Mira Loma, a semi-urban area in southern California. The most abundant species were found to be sulfur (S; 23% of the total trace element concentration), followed by Si, Fe, Ca, and Al (soil-related elements; 51% of the total). In general, total trace element concentrations were found to be significantly higher for the drier months of September and October, compared to December and January. Factor analysis, enrichment factor (EF) analysis, and ratio analysis (Al/Zn) revealed a significant contribution of soil-related sources to the ambient trace elements for PM2.5 in the study area. Other important contributors to the trace elements in ambient PM2.5 in Mira Loma included motor vehicle-related emissions (brake pads, lubricant oils, gasoline, and diesel combustion), secondary sulfates, sea salts, and biomass burning. The influence of sea salts on the study area was identified using a backward trajectory analysis.  相似文献   

7.

This study presents the chemical composition (carbonaceous and nitrogenous components) of aerosols (PM2.5 and PM10) along with stable isotopic composition (δ13C and δ15N) collected during winter and the summer months of 2015–16 to explore the possible sources of aerosols in megacity Delhi, India. The mean concentrations (mean?±?standard deviation at 1σ) of PM2.5 and PM10 were 223?±?69 µg m?3 and 328?±?65 µg m?3, respectively during winter season whereas the mean concentrations of PM2.5 and PM10 were 147?±?22 µg m?3 and 236?±?61 µg m?3, respectively during summer season. The mean value of δ13C (range: ??26.4 to ??23.4‰) and δ15N (range: 3.3 to 14.4‰) of PM2.5 were ??25.3?±?0.5‰ and 8.9?±?2.1‰, respectively during winter season whereas the mean value of δ13C (range: ??26.7 to ??25.3‰) and δ15N (range: 2.8 to 11.5‰) of PM2.5 were ??26.1?±?0.4‰ and 6.4?±?2.5‰, respectively during the summer season. Comparison of stable C and N isotopic fingerprints of major identical sources suggested that major portion of PM2.5 and PM10 at Delhi were mainly from fossil fuel combustion (FFC), biomass burning (BB) (C-3 and C-4 type vegitation), secondary aerosols (SAs) and road dust (SD). The correlation analysis of δ13C with other C (OC, TC, OC/EC and OC/WSOC) components and δ15N with other N components (TN, NH4+ and NO3?) are also support the source identification of isotopic signatures.

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8.
In this paper we present results of a numerical study using the NASA finite-volume GCM to elucidate a plausible mechanism for aerosol impact on the Asian summer monsoon involving interaction with physical processes over the Tibetan Plateau (TP). During the pre-monsoon season of March–April, dusts from the deserts of western China, Afghanistan/Pakistan, and the Middle East are transported into and stacked up against the northern and southern slopes of the TP. The absorption of solar radiation by dust heats up the elevated surface air over the slopes. On the southern slopes, the atmospheric heating is reinforced by black carbon from local emission. The heated air rises via dry convection, creating a positive temperature anomaly in the mid-to-upper troposphere over the TP relative to the region to the south. In May through early June in a manner akin to an “elevated heat pump”, the rising hot air forced by the increasing heating in the upper troposphere, draws in warm and moist air over the Indian subcontinent, setting the stage for the onset of the South Asia summer monsoon. Our results suggest that increased dust loading coupled with black carbon emission from local sources in northern India during late spring may lead to an advance of the rainy periods and subsequently an intensification of the Indian summer monsoon. The enhanced rainfall over India is associated with the development of an aerosol-induced large-scale sea level pressure anomaly pattern, which causes the East Asia (Mei-yu) rain belt to shift northwestward, suppressing rainfall over East Asia and the adjacent oceanic regions.  相似文献   

9.
The manual harvest of sugar cane requires the burning of its foliage. This burning has strongly increased in Brazil after the National Alcohol Program was started which substituted automobile gasoline engines for alcohol engines. Presently, the source strength per unit area of this rural pollution is comparable to the well-known biomass burning source in Amazonia. The observed concentrations of CO and O3 in the rural area of the state of São Paulo during the 1988 burning season were twice as large as those reported from an aircraft experiment of 1985 for biomass burnings of the tropical rain forest. Results are reported from airplane measurements and from three fixed ground stations. Mixing ratios of ozone and carbon monoxide in the height range below 6 km are normally less than 40 and 100 ppbv, (parts per billion by volume), respectively, in the absence of burnings. A strong O3 and CO layer was observed during the burning period with peak concentrations of 80 ppbv of ozone and 580 ppbv of CO at about 2 km. The concentrations of CH4 and CO2 were also large, 1756 ppbv and 409 ppmv, respectively, at 1500 m. During the dry season period of the experiment, the ground based O3 average diurnal variations obtained at the rural sites were practically identical to the typical urban variation observed at São José dos Campos, with daytime ozone values between 45 and 60 ppbv. A second three-day airplane excursion to the surgar cane fields in the wet season of 1989 has produces results to be contrasted with the dry (burning) season of 1988 and 1989. Carbon monoxide concentrations were below 100 ppbv at all heights and ozone concentrations were around 30–40 ppbv. The maximum daytime concentrations at the ground station Bauru was 25 ppbv of O3, and at Jaboticabal it was 35 ppbv of O3, only one half of what was observed in the dry season.Universidade Estadual de São Paulo.  相似文献   

10.
Haze-fog conditions over northern India are associated with visibility degradation and severe attenuation of solar radiation by airborne particles with various chemical compositions. PM2.5 samples have been collected in Delhi, India from December 2011 to November 2012 and analyzed for carbonaceous and inorganic species. PM10 measurements were made simultaneously such that PM10–2.5 could be estimated by difference. This study analyzes the temporal variation of PM2.5 and carbonaceous particles (CP), focusing on identification of the primary and secondary aerosol emissions, estimations of light extinction coefficient (bext) and the contributions by the major PM2.5 chemical components. The annual mean concentrations of PM2.5, organic carbon (OC), elemental carbon (EC) and PM10–2.5 were found to be 153.6 ± 59.8, 33.5 ± 15.9, 6.9 ± 3.9 and 91.1 ± 99.9 μg m?3, respectively. Total CP, secondary organic aerosols and major anions (e.g., SO4 2? and NO3 ?) maximize during the post-monsoon and winter due to fossil fuel combustion and biomass burning. PM10–2.5 is more abundant during the pre-monsoon and post-monsoon. The OC/EC varies from 2.45 to 9.26 (mean of 5.18 ± 1.47), indicating the influence of multiple combustion sources. The bext exhibits highest values (910 ± 280 and 1221 ± 371 Mm?1) in post-monsoon and winter and lowest in monsoon (363 ± 110 and 457 ± 133 Mm?1) as estimated via the original and revised IMPROVE algorithms, respectively. Organic matter (OM =1.6 × OC) accounts for ~39 % and ~48 % of the bext, followed by (NH4)2SO4 (~21 % and ~24 %) and EC (~13 % and ~10 %), according to the original and revised algorithms, respectively. The bext estimates via the two IMPROVE versions are highly correlated (R2 = 0.95, root mean square error = 38 % and mean bias error = 28 %) and are strongly related to visibility impairment (r = ?0.72), mostly associated with anthropogenic rather than natural PM contributions. Therefore, reduction of CP and precursor gas emissions represents an urgent opportunity for air quality improvement across Delhi.  相似文献   

11.
夏季亚洲季风区是对流层向平流层物质输送的主要通道,其对平流层水汽的变化有重要贡献。以往的研究表明亚洲季风区向平流层的水汽传输主要在青藏高原及周边地区。本文利用多年平均的逐日ERAi、MERRA再分析数据和微波临边观测仪(Microwave Limb Sounder,MLS)数据,首先对比分析夏季青藏高原周边上空水汽的分布特征,再利用再分析资料分析了对流层—平流层水汽传输的特征。结果表明:青藏高原周边特定的等熵面和对流层顶结构分布有利于水汽向平流层的绝热输送;在南亚高压的东北侧,从青藏高原到中太平洋地区,340~360 K层次存在最为显著的水汽向平流层的纬向等熵绝热输送通道,7~8月平均输送强度可达约7×103 kg s-1。此外,在伊朗高原及南亚高压的西部,350~360 K层次也存在一支水汽向平流层的经向等熵绝热输送通道,但强度相对较弱(约2.5×103 kg s-1)。在青藏高原南侧370~380 K层次存在强的水汽向平流层的非绝热输送,主要由深对流和大尺度上升运动引起,7~8月平均输送强度约0.4×103 kg s-1。落基山以东到大西洋西部,350~360 K层次存在水汽向平流层的纬向等熵绝热输送通道,但强度也弱得多(约2.5×103 kg s-1)。  相似文献   

12.
Climate change modulates surface concentrations of fine particulate matter (PM2.5) and ozone (O3), indirectly affecting premature mortality attributed to air pollution. We estimate the change in global premature mortality and years of life lost (YLL) associated with changes in surface O3 and PM2.5 over the 21st century as a result of climate change. We use a global coupled chemistry-climate model to simulate current and future climate and the effect of changing climate on air quality. Epidemiological concentration-response relationships are applied to estimate resulting changes in premature mortality and YLL. The effect of climate change on air quality is isolated by holding emissions of air pollutants constant while allowing climate to evolve over the 21st century according to a moderate projection of greenhouse gas emissions (A1B scenario). Resulting changes in 21st century climate alone lead to an increase in simulated PM2.5 concentrations globally, and to higher (lower) O3 concentrations over populated (remote) regions. Global annual premature mortality associated with chronic exposure to PM2.5 increases by approximately 100 thousand deaths (95 % confidence interval, CI, of 66–130 thousand) with corresponding YLL increasing by nearly 900 thousand (95 % CI, 576–1,128 thousand) years. The annual premature mortality due to respiratory disease associated with chronic O3 exposure increases by +6,300 deaths (95 % CI, 1,600–10,400). This climate penalty indicates that stronger emission controls will be needed in the future to meet current air quality standards and to avoid higher health risks associated with climate change induced worsening of air quality over populated regions.  相似文献   

13.
This study investigates the capability of the dynamic downscaling method (DDM) in an East Asian climate study for June 1998 using the fifth-generation Pennsylvania State University-National Center for Atmospheric Research non-hydrostatic Mesoscale Model (MM5).Sensitivity experiments show that MM5 results at upper atmospheric levels cannot match reanalyses data,but the results show consistent improvement in simulating moisture transport at low levels.The downscaling ability for precipitation is regionally dependent.During the monsoon season over the Yangtze River basin and the pre-monsoon season over North China,the DDM cannot match observed precipitation.Over Northwest China and the Tibetan Plateau (TP),where there is high topography,the DDM shows better performance than reanalyses.Simulated monsoon evolution processes over East Asia,however,are much closer to observational data than reanalyses.The convection scheme has a substantial impact on extreme rainfall over the Yangtze River basin and the pre-monsoon over North China,but only a marginal contribution for Northwest China and the TP.Land surface parameterizations affect the locations and pattern of rainfall bands.The 10-day re-initialization in this study shows some improvement in simulated precipitation over some sub-regions but with no obvious improvement in circulation.The setting of the location of lateral boundaries (LLB) westward improves performance of the DDM.Including the entire TP in the western model domain improves the DDM performance in simulating precipitation in most sub-regions.In addition,a seasonal simulation demonstrates that the DDM can also obtain consistent results,as in the June case,even when another two months consist of no strong climate/weather events.  相似文献   

14.
PM10 samples were collected to characterize the seasonal and annual trends of carbonaceous content in PM10 at an urban site of megacity Delhi, India from January 2010 to December 2017. Organic carbon (OC) and elemental carbon (EC) concentrations were quantified by thermal-optical transmission (TOT) method of PM10 samples collected at Delhi. The average concentrations of PM10, OC, EC and TCA (total carbonaceous aerosol) were 222?±?87 (range: 48.2–583.8 μg m?3), 25.6?±?14.0 (range: 4.2–82.5 μg m?3), 8.7?±?5.8 (range: 0.8–35.6 μg m?3) and 54.7?±?30.6 μg m?3 (range: 8.4–175.2 μg m?3), respectively during entire sampling period. The average secondary organic carbon (SOC) concentration ranged from 2.5–9.1 μg m?3 in PM10, accounting from 14 to 28% of total OC mass concentration of PM10. Significant seasonal variations were recorded in concentrations of PM10, OC, EC and TCA with maxima during winter and minima during monsoon seasons. In the present study, the positive linear trend between OC and EC were recorded during winter (R2?=?0.53), summer (R2?=?0.59) and monsoon (R2?=?0.78) seasons. This behaviour suggests the contribution of similar sources and common atmospheric processes in both the fractions. OC/EC weight ratio suggested that vehicular emissions, fossil fuel combustion and biomass burning could be the major sources of carbonaceous aerosols of PM10 at the megacity Delhi, India. Trajectory analysis indicates that the air mass approches to the sampling site is mainly from Indo Gangetic plain (IGP) region (Uttar Pradesh, Haryana and Punjab etc.), Thar desert, Afghanistan, Pakistan and surrounding areas.  相似文献   

15.
碳质气溶胶在藏东南冰芯中的记录   总被引:2,自引:0,他引:2       下载免费PDF全文
在青藏高原东南部帕隆藏布源头海洋性冰川区,对冰川编目的4号冰川(PLZ-4)实施冰芯钻取,获得总长度为29 m的冰芯。对冰芯中元素碳(EC)、不溶性有机碳(WIOC)和可溶性离子(Cl-,NO3-,SO42-,Na+,K+,Mg2+,Ca2+)的含量进行实验分析,结果显示:1998-2005年上述组分在该冰芯中的含量均呈现持续增长的趋势;冰芯中EC含量及EC/WIOC比值表现出非季风季节高、季风季节低的显著特征,揭示了该地区冰川中记录的碳质气溶胶浓度与南亚棕色云之间的密切联系。同时指出,在季风前的4-5月,沉降于雪冰中平均含量>10 ng/g的EC所引起的雪冰表面反照率降低以及冰川消融等气候环境效应不容忽视。  相似文献   

16.
Aerosols consist of organic and inorganic species, and the composition and concentration of these species depends on their sources, chemical transformation and sinks. In this study an assessment of major inorganic ions determined in three aerosol particle size ranges collected for 1 year at Welgegund in South Africa was conducted. SO42? and ammonium (NH4+) dominated the PM1 size fraction, while SO42? and nitrate (NO3) dominated the PM1–2.5 and PM2.5–10 size fractions. SO42? had the highest contribution in the two smaller size fractions, while NO3? had the highest contribution in the PM2.5–10 size fraction. SO42? and NO3? levels were attributed to the impacts of aged air masses passing over major anthropogenic source regions. Comparison of inorganic ion concentrations to levels thereof within a source region influencing Welgegund, indicated higher levels of most species within the source region. However, the comparative ratio of SO42? was significantly lower due to SO42? being formed distant from SO2 emissions and submicron SO42? having longer atmospheric residencies. The PM at Welgegund was determined to be acidic, mainly due to high concentrations of SO42?. PM1 and PM1–2.5 fractions revealed a seasonal pattern, with higher inorganic ion concentrations measured from May to September. Higher concentrations were attributed to decreased wet removal, more pronounced inversion layers trapping pollutants, and increases in household combustion and wild fires during winter. Back trajectory analysis also revealed higher concentrations of inorganic ionic species corresponding to air mass movements over anthropogenic source regions.  相似文献   

17.
Studies on air pollution and climate change have shown that forest fires constitute one of the major sources of atmospheric trace gases and particulate matter, especially during the dry season. However, these emissions remain difficult to quantify due to uncertainty on the extent of burned areas and deficient knowledge on the forest fire behaviours in each country. This study aims to estimate emissions from forest fires in Thailand by using the combination of the Moderate Resolution Imaging Spectroradiometer (MODIS) for active fire products and country-specific data based on prescribed burning experiments. The results indicate that 27817 fire hotspots (FHS) associated with forest fires were detected by the MODIS during 2005–2009. These FHS mainly occurred in the northern, western, and upper north-eastern parts of Thailand. Each year, the most significant fires were observed during January–May, with a peak in March. The majority of forest FHS were detected in the afternoon. According to the prescribed burning experiments, the average area of forest burned per fire event was found to fall within the range 1.09 to 12.47 ha, depending upon the terrain slope and weather conditions. The total burned area was computed at 159309 ha corresponding to the surface biomass fuel of 541515 tons dry matter. The forest fire emissions were computed at 855593 tons of CO2, 56318 tons of CO, 3682 tons of CH4, 108 tons of N2O, 4928 tons of PM2.5, 4603 tons of PM10, 357 tons of BC and 2816 tons of OC.  相似文献   

18.
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   

19.
The influence of soil moisture on Asian monsoon simulation/prediction was less studied, partly due to a lack of available and reliable soil moisture datasets. In this study, we firstly compare several soil moisture datasets over the Tibetan Plateau, and find that the remote sensing products from the Advanced Microwave Scanning Radiometer for Earth Observing System (AMSR-E) can capture realistic temporal variations of soil moisture better than the two reanalyses (NCEP and ECMWF) during the pre-monsoon season...  相似文献   

20.
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   

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