Urban Air Pollution Monitoring with DOAS Considering the Local Meteorological Situation

The concentrations of ozone, NO₂ and SO₂, measured with a DOAS system 70 m above ground level in the city of Graz were compared with data from conventional ground stations. The dependence of vertical trace-gas distributions on stability categories and time of the day or year was investigated. Concerning the maximum ozone concentrations in summer, the DOAS data are representative for the ground-level situation. In average, the concentrations 70 m above ground are more than twice the ground-level concentrations. It has been shown that beside the reaction with NO, dry deposition is an important sink for ozone near the surface. The DOAS NO₂-concentrations are representative for ground-level conditions in summer, except for the morning maximum of NO₂. In winter the DOAS NO₂-concentrations amount for 73% of the ground level values in average. Concerning the slow reacting trace gas SO₂, the DOAS data are always representative for the ground-level conditions.     

北京市高海拔地区百花山空气质量状况及与市区的差异性研究

对北京市远郊百花山(海拔1300 m)2007—2017年大气常规6项污染物数据进行了分析,并与代表市区的国控站点均值数据进行了比较。研究发现,百花山SO2、CO、PM2.5浓度为国控站点浓度的35.5%~35.7%,NO2、PM 10、O 3浓度分别为国控站点浓度的14.0%、41.5%、185.5%。11年间,百花山6项常规污染物浓度逐年降低。2013—2017年,百花山PM2.5浓度年均降速为11.4%,低于国控站点13.3%的年均改善水平。百花山和国控站点在污染物季节变化趋势上基本一致,秋季颗粒物浓度差异最大,春季差异最小。百花山6项污染物的日变化峰谷比值为1.21~1.44,其差异小于国控站点。各项污染物浓度在18:00出现峰值,认为主要受城区远距离传输影响。2013—2017年,百花山共出现5个PM2.5重污染天,5级以上重污染小时数为442 h,国控站点有2%的重污染小时与百花山同步。     

The Seasonal Variation of the Concentrations of Ozone, Sulfur Dioxide, and Nitrogen Oxides in Two Nigerian Cities

A combination of multivariate statistical methods including factor analysis, principal component analysis, principal component regression, and multiple linear regression (MLR) were employed to evaluate the influence of seasons on the concentrations of ozone, sulfur (IV) oxide, and oxides of nitrogen in ambient air of Nigerian cities of Lagos and Ilorin. The former city is located in the coastal area, and it is highly congested with a high intensity of marine, vehicular, and industrial activities, and the latter city is a medium size town, located in the central guinea savannah zone of Nigeria. Samples were collected using a high-volume sampler from near the ground at various sites of diverse human and industrial activities, during wet and dry seasons from 2003 to 2006. The PCA reveals three distinct groupings during the day for all data, which is a reflection of different factors contributing to the atmospheric chemistry of these cities. The predicted ozone concentration values by MLR agree fairly well with the measured data. The dependence of ozone on meteorological parameters including relative humidity, air temperature, and sun exposure and the precursor pollutants depends on weather and the anthropogenic activities. The results for the two cities indicate that reduction in the level of NO₂ is accompanied by an increase in the level of ozone, suggesting the interconversion between the two via photochemical activity.     

Accuracy of bottled drinking water label content

The accurate predictions of ground ozone concentrations are required for proper management, control, and making public warning strategies. Due to the difficulties in handling phenomenological models that are based on complex chemical reactions of ozone production, neural network models gained popularity in the last decade. These models also have some limitations due to problems of overfitting, local minima, and tuning of network parameters. In this study, the predictions of daily maximum ozone concentrations are attempted using support vector machines (SVMs). The comparison between the accuracy of SVM and neural network predictions is performed to evaluate their performance. For this, the daily maximum ozone concentration data observed during 2002–2004 at a site in Delhi is utilized. The models are developed using the available meteorological parameters. The results indicated the promising performance of SVM over neural networks in predicting daily maximum ozone concentrations.     

A study of ground-level ozone pollution, ozone precursors and subtropical meteorological conditions in central Taiwan

Hourly concentrations of ozone (O(3)), 55 volatile organic compounds (VOCs, ozone precursors) and nitrogen oxides (NOx) were measured at an upwind urban site, a downwind suburban site, and a rural site in central Taiwan, from January 2003 to December 2006. VOC and NOx mean concentrations showed a gradient from high to low across the urban (56 ppb and 34 ppb), suburban (38 ppb and 27 ppb) and rural sites (25 ppb and 21 ppb) but a reverse gradient in ozone across these sites (24, 27, and 29 ppb, respectively). Although there was about twice the difference in VOC concentrations between the urban and rural sites, nearly 65% ozone formation potential was contributed to by the same 9 VOCs. Seasonal patterns showed peak ozone levels in autumn and minima in summer at the urban site, but minima in winter at the downwind suburban and rural sites. Ozone precursor levels, on the other hand, were lowest in summer and highest in winter. The diurnal pattern showed that ozone levels peaked one hour later at the rural site than at the urban site. The ethylbenzene to m,p-xylene ratio, an indicator of the age of the air mass, increased from 0.4 at the urban site to 0.6 at the suburban site and 0.8 at the rural site during daily peak ozone times. This finding suggests the transport of ozone and precursors from upwind to downwind producing elevated ozone levels in the suburban and rural areas. Ozone episodes occurred mostly in days with a mean midday UV index of 6.5 (1 UV index=100 J m(-2)) and wind speed at 1.3 m s(-1) at all three sites.     

成都市夏季近地面臭氧污染气象特征

利用2016年7月成都市8个环境监测站点的臭氧、NO_2的监测资料以及成都市国家基准气象站和基本气象站的观测资料,对成都市夏季臭氧、NO_2浓度和气象要素的日变化特征和臭氧污染过程进行了分析。研究结果表明:成都市臭氧污染受综合气象条件和NO_2浓度的影响,高温、低湿、强辐射有利于臭氧大量生成,NO_2浓度高低决定了臭氧浓度的峰值大小;在污染期间,大气边界层高度远高于本地平均水平,数值约为平均水平的2～3倍;成都市臭氧污染的主要影响因子存在地区差异,成都市区的臭氧主要来自于自身的光化学反应,而灵岩寺地区的臭氧来自于VOCs和大气水平输送。     

Spatial and temporal variation of surface ozone,NO and NO2 at urban,suburban, rural and industrial sites in the southwest of the Iberian Peninsula

Surface ozone is one of the most important photochemical pollutants in the low atmosphere, causing damage to human health, vegetation, materials and climate. The weather (high temperatures and high solar radiation), orography (presence of the Guadalquivir valley) and anthropogenic (the cities of Cádiz, Córdoba, Huelva and Seville and two important industrial complexes) characteristics of the southwestern Iberian Peninsula make this region ideal for the formation and accumulation of ozone. To increase the knowledge of ozone behaviour in this area, the monthly, daily and weekly variations of ozone and its precursors, nitrogen oxides (NO_x?=?NO?+?NO₂), were analysed over a 4-year period (2003 to 2006). Using the k-means cluster technique, 12 representative stations of five different areas with different ozone behaviour were selected from a total of 29 monitoring sites. This is the first time that the analysis of these atmospheric pollutants has been carried out for the whole area, allowing therefore a complete understanding of the dynamics and the relationships of these compounds in this region. The results showed an opposite behaviour among ozone and NO and NO₂ concentrations in urban and suburban zones, marked by maximums of ozone (minimums NO_x) in spring and summer and minimums (maximums) in autumn and winter. A seasonal behaviour, with lower amplitude, was also observed in rural and industrial areas for ozone concentrations, with the NO and NO₂ concentrations remaining at low and similar values during the year in rural zones due to the absence of emission sources in their surroundings. The daily cycles of ozone in urban, suburban and industrial sites registered a maximum value in the early afternoon (14:00–17:00 UTC) while for NO_x two peaks were observed, at 7:00–10:00 UTC and 20:00–22:00. In the case of rural stations, no hourly peak of ozone or NO_x was registered. The weekend effect was studied by using a statistical contrast tests (Student’s t). The results indicated that only areas influenced by important traffic emissions presented a weekend effect for NO and NO₂, whereas an ozone weekend effect was not detected in any case.     

基于EOF/SVD的2018年湖北省臭氧特征及其高值与气象要素关系研究

基于湖北省2018年4-10月臭氧、温度和相对湿度逐小时监测数据以及50 m风场逐小时再分析数据,采用经验正交函数(EOF)和奇异值分解(SVD)方法,分析了2018年湖北省臭氧特征及其高值与气象要素关系。结果表明:湖北省臭氧日最大8 h浓度距平呈现以武汉为正值中心、自鄂东向鄂西递减的主要空间分布型;15:00臭氧与温度呈现较好的正相关关系,以随州、襄阳及其周边最为明显;与14:00相对湿度呈现很好的负相关关系,以孝感、随州、荆门及其周边最为明显;襄阳西部和十堰北部地区15:00 50 m风场的纬向分量对本地臭氧高值有一定影响,武汉北部、黄冈北部以及孝感东部等地15:00 50 m风场的经向分量对本地臭氧高值影响较大。     

Distribution and Fractionation of Heavy Metals in Solid Waste from Selected Sites in the Industrial Belt of Delhi, India

Solid waste samples were collected from five small-scale industrial sites in the National Capital Territory (NCT) of Delhi. These industrial sites represent the regional spread of the industrial belt in the NCT of Delhi. Solid waste samples were digested using aqua-regia and HF in air tight teflon bombs for the quantitative analysis of heavy metals (Hg, Pb, Cd, Mn, Fe, Ni, Cu and Zn) by GBC model 902 atomic absorption spectrophotometer. Hg was analysed using hydrid generator attachment. Beside this sequential extraction was used to fractionate five heavy metals (Pb, Ni, Cd, Cu and Zn) into six operationally defined phases, viz. water soluble, exchangeable, carbonate-bound, Fe-Mn oxides, organic-bound and residual fractions to ascertain the relative mobility of these metals. The result obtained showed metal concentration to be in the range of Hg 0.42-2.3; Pb 23-530; Cd 014-224; Mn 494-19 964; Fe 35 684-233 119; Ni 192-1534; Cu 3065-10 144 and Zn 116-23 321 (all units in mg kg(-1)) in all the industrial areas studied. The fractionated toxic metals like Pb, Ni and Cd were observed to be in the range of 25-35, 15-50 and 40-50%, respectively, in mobile or bio-available fractions of solid waste. As this waste is often disposed-off by the roadsides, low lying areas, abandoned quarries or in landfill sites which are often not properly planned, thus posing potential risk to ground and surface water quality to millions of people living downstream.     

Profile of PAHs in the inhalable particulate fraction: source apportionment and associated health risks in a tropical megacity

The present study proposed to investigate the atmospheric distribution, sources, and inhalation health risks of polycyclic aromatic hydrocarbons (PAHs) in a tropical megacity (Delhi, India). To this end, 16 US EPA priority PAHs were measured in the inhalable fraction of atmospheric particles (PM₁₀; aerodynamic diameter, ≤10 μm) collected weekly at three residential areas in Delhi from December 2008 to November 2009. Mean annual 24 h PM₁₀ levels at the sites (166.5–192.3 μg m^?3) were eight to ten times the WHO limit. Weekday/weekend effects on PM₁₀ and associated PAHs were investigated. Σ₁₆PAH concentrations (sum of 16 PAHs analyzed; overall annual mean, 105.3 ng m^?3; overall range, 10.5–511.9 ng m^?3) observed were at least an order of magnitude greater than values reported from European and US cities. Spatial variations in PAHs were influenced by nearness to traffic and thermal power plants while seasonal variation trends showed highest concentrations in winter. Associations between Σ₁₆PAHs and various meteorological parameters were investigated. The overall PAH profile was dominated by combustion-derived large-ring species (85–87 %) that were essentially local in origin. Carcinogenic PAHs contributed 58–62 % to Σ₁₆PAH loads at the sites. Molecular diagnostic ratios were used for preliminary assessment of PAH sources. Principal component analysis coupled with multiple linear regression-identified vehicular emissions as the predominant source (62–83 %), followed by coal combustion (18–19 %), residential fuel use (19 %), and industrial emissions (16 %). Spatio-temporal variations and time-evolution of source contributions were studied. Inhalation cancer risk assessment showed that a maximum of 39,780 excess cancer cases might occur due to lifetime inhalation exposure to the analyzed PAH concentrations.     

Prediction of daily ground-level ozone concentration maxima over New Delhi

The pollution levels in New Delhi from industrial, residential, and transportation sources are continuously growing. As one of the major pollutants, ground-level ozone is responsible for various adverse effects on both humans and foliage. The present study aims to predict daily ground-level ozone concentration maxima over a site situated in New Delhi through neural networks (NN) and multiple-regression (MR) analysis. Although these methodologies are case and site specific, they are being developed and used widely. Therefore, to test these methodologies for New Delhi where no such study is available for ground-level ozone, six models have been developed based on NNs and MR using the same input data set. The changes in the performance capability of the two methods are sensitive to the selection of input parameters. The results are encouraging, and remarkable improvements in the performance of the models have been observed.     

Preparation and Validation of Gridded Emission Inventory of Criteria Air Pollutants and Identification of Emission Hotspots for Megacity Delhi

Delhi is one of the many megacities struggling with punishing levels of pollution from industrial, residential, and transportation sources. Over the years, pollution abatement in Delhi has become an important constituent of state policies. In the past one decade a lot of policies and regulations have been implemented which have had a noticeable effect on pollution levels. In this context, air quality models provide a powerful tool to study the impact of development plans on the expected air pollution levels and thus aid the regulating and planning authorities in decision-making process. In air quality modeling, emissions in the modeling domain at regular interval are one of the most important inputs. From the annual emission data of over a decade (1990–2000), emission inventory is prepared for the megacity Delhi. Four criteria pollutants namely, CO, SO₂, PM, and NO _x are considered and a gridded emission inventory over Delhi has been prepared taking into account land use pattern, population density, traffic density, industrial areas, etc. A top down approach is used for this purpose. Emission isopleths are drawn and annual emission patterns are discussed mainly for the years 1990, 1996 and 2000. Primary and secondary areas of emission hotspots are identified and emission variations discussed during the study period. Validation of estimated values is desired from the available data. There is a direct relationship of pollution levels and emission strength in a given area. Hence, an attempt has been made to validate the emission inventory for all criteria pollutants by analyzing emissions in various sampling zones with the ambient pollution levels. For validation purpose, the geographical region encompassing the study area (Delhi) has been divided into seven emission zones as per the air quality monitoring stations using Voronoi polygon concept. Dispersion modeling is also used for continuous elevated sources to have the contributing emissions at the ground level to facilitate validation. A good correlation between emission estimates and concentration has been found. Correlation coefficient of 0.82, 0.77, 0.58 and 0.68 for CO, SO₂, PM and NO _x respectively shows a reasonably satisfactory performance of the present estimates.     

An assessment of air quality in Karachi,Pakistan

An atmospheric pollution survey was carried out at 13 sites in Karachi, Pakistan, simultaneously from 0600 h to 2100 h for 15 consecutive days in May 1990 which also included meteorological measurements. The monitoring sites were included along the prevailing wind patterns in Karachi. Carbon monoxide levels in the ambient air were found to reach 9–10 ppm along the busy urban streets whereas CO₂ level exceeded 370 ppm in these areas. Our survey indicates that NO₂ levels were exceeding U.S. ambient air quality standards. Maxmum NO₂ concentrations were observed (0.3–0.5 ppm) during the daytime from 0600 h to 2100 h. The surface ozone maximum around noon at the inland sites reached the levels of 40 ppb and 50 ppb respectively compared to upwind coastal Sites 1 level of 25 ppb. The Pb concentrations were approximately 3- to 7-fold higher than average, which corresponded well to urban air. Fossil fuel SO₄ (excess) and NO₃ were apportionally based on the assumption that these two anions were present as (NH₄)₂SO₄, and NH₄NO₃ in the aerosols. In the eastern part of the city atmospheric sulphate (SO₄) shows the combustion of coal as its source from the vicinity and downwind of a steel manufacturing plant.     

Study of temporal variation in ambient air quality during Diwali festival in India

The variation in air quality was assessed from the ambient concentrations of various air pollutants [total suspended particle (TSP), particulate matter ≤10 μm (PM₁₀), SO₂, and NO₂] for pre-Diwali, Diwali festival, post-Diwali, and foggy day (October, November, and December), Delhi (India), from 2002 to 2007. The extensive use of fireworks was found to be related to short-term variation in air quality. During the festival, TSP is almost of the same order as compared to the concentration at an industrial site in Delhi in all the years. However, the concentrations of PM₁₀, SO₂, and NO₂ increased two to six times during the Diwali period when compared to the data reported for an industrial site. Similar trend was observed when the concentrations of pollutants were compared with values obtained for a typical foggy day each year in December. The levels of these pollutants observed during Diwali were found to be higher due to adverse meteorological conditions, i.e., decrease in 24 h average mixing height, temperature, and wind speed. The trend analysis shows that TSP, PM₁₀, NO₂, and SO₂ concentration increased just before Diwali and reached to a maximum concentration on the day of the festival. The values gradually decreased after the festival. On Diwali day, 24-h values for TSP and PM₁₀ in all the years from 2002 to 2007 and for NO₂ in 2004 and 2007 were found to be higher than prescribed limits of National Ambient Air Quality Standards and exceptionally high (3.6 times) for PM₁₀ in 2007. These results indicate that fireworks during the Diwali festival affected the ambient air quality adversely due to emission and accumulation of TSP, PM₁₀, SO₂, and NO_2.     

Comparative spray drift studies of aerial and ground applications 1983–1985

The amount of off-site pesticide spray drift from aerial and ground applications was determined at 26 sites across Ontario. These were conducted along transects, parallel and at right angles to the flight path during aerial spray applications and at right angles to the direction of ground spray applications. All sites monitored were where commercial spray operations were in progress. The aerial applications involved both fixed wing aircraft and helicopters and the ground applications involved concentrated air-blast machines and high and low pressure boom sprayers. Deposits of spray drift outside the target area were common to all spray equipment monitored. All except low-pressure boom spraying equipment resulted in measurable spray drift to 80 m off-target with appreciable deposits up to 30–40 m. In a forest spray operation, where insecticide release was the highest, measurable residues were found up to 120 m off-target. The amount of chemical deposited off-target varied with the chemical, the climatical conditions and the equipment used. With a low-pressure boom sprayer, serious drift was confined to 9 m off-target and measurable residues to 15 m.     

Variation of Surface Ozone in the Ambient Air of Auckland, New Zealand

A study has been performed on the characteristics and behavior of surface ozone concentrations at four monitoring sites in Auckland, New Zealand (37 degrees S, 174.8 degrees E) for a four-year period (October 1997-October 2001). One monitoring site (rural) was located upwind of the Auckland urban complex, a second downwind (rural-coastal), and a third within the urban area, while the fourth was an elevated urban-city site located 250 m up the Sky Tower in the central city. In contrast to the high elevation site, the diurnal behaviour of ozone at the three low elevation sites followed a typical solar radiation cycle with high ozone during the day and low nocturnal values. The effect of NO(x) titration was distinct at the urban sites. There was also a seasonal variability in the measured ozone levels with high concentrations in spring and a significant summer minimum. The observed surface ozone concentrations in Auckland were significantly lower than other cities of the world, although a potential for high oxidant formation existed. Observed ozone episodes appear to have been either generated locally or the precursors transported via the prevailing southwest wind. A unique feature of Auckland's air quality is the dilution of polluted city air due to the mixing of east-coast air into the clean west-coast circulation leading to the overall lower average concentrations in summer. A second feature is the potential interaction between sea salt particles and ozone that may provide an additional ozone loss mechanism.     

Assessing effects of ambient ozone on injury and yield of bean with ethylenediurea (EDU): three years of plant monitoring at four sites in The Netherlands

EDU (ethylenediurea) and non-EDU-treated bean plants (Phaseolus vulgaris) L. cv. Lit) were exposed to ambient air at four rural sites in the Netherlands during the growing seasonsof 1994 through 1996 to investigate the responses to ambient ozone. Ozone-induced foliar injury was observed each year anddifferences in injury between sites depended on year. On average,injury amounted to 27% in 1994, to 8% in 1995 and to 1% in 1996. Injury increased with increasing ozone exposure (AOT40) and the estimated AOT40 value corresponding with 5% injury wascirca 3650 nl l^-1 h ozone. The highest ozone levels accumulated at each site for five consecutive days before injuryexceeded the proposed short-term critical level for injury development. EDU reduced injury and its protective effect was positively related to the injury intensity in non-EDU-treatedplants. Yield of green marketable pods (intermediate harvest) andmature pods (final harvest) was generally reduced in non-EDU-treated plants compared to EDU-treated plants and differences inyield reduction between harvests varied between years. The yield of mature pods was reduced in 1994 and 1996 while the yield ofgreen pods was reduced in 1995 by ozone only. Since yield reduction was not correlated with AOT40, the EDU method was notvalid to determine an ozone exposure-yield reponse relationshipfor bean.     

Assessment of Air Quality After the Implementation of Compressed Natural Gas (CNG) as Fuel in Public Transport in Delhi, India

Public transport in Delhi was amended by the Supreme Court of India to use Compressed Natural Gas (CNG) instead of diesel or petrol. After the implementation of CNG since April 2001, Delhi has the highest fraction of CNG-run public vehicles in the world and most of them were introduced within 20 months. In the present study, the concentrations of various criteria air pollutants (SPM, PM₁₀, CO, SO₂ and NO_x) and organic pollutants such as benzene, toluene, xylene (BTX) and polycyclic aromatic hydrocarbons (PAHs) were assessed before and after the implementation of CNG. A decreasing trend was found for PAHs, SO₂ and CO concentrations, while the NO_x level was increased in comparison to those before the implementation of CNG. Further, SPM, PM₁₀, and BTX concentrations showed no significant change after the implementation of CNG. However, the BTX concentration demonstrated a clear relation with the benzene content of gasoline. In addition to the impact of the introduction of CNG the daily variation in PAHs levels was also studied and the PAHs concentrations were observed to be relatively high between 10 pm to 6 am, which gives a proof of a relation with the limited day entry and movement of heavy vehicles in Delhi.     

Suspended Particulate Matter Distribution in Rural-Industrial Satna and in Urban-Industrial South Delhi

An air quality sampling program was designed and implemented to collect the baseline concentrations of respirable suspended particulates (RSP = PM₁₀), non-respirable suspended particulates (NRSP) and fine suspended particulates (FSP = PM_2.5). Over a three-week period, a 24-h average concentrations were calculated from the samples collected at an industrial site in Southern Delhi and compared to datasets collected in Satna by Envirotech Limited, Okhla, Delhi in order to establish the characteristic difference in emission patterns. PM_2.5, PM₁₀, and total suspended particulates (TSP) concentrations at Satna were 20.5 ± 6.0, 102.1 ± 41.1, and 387.6 ± 222.4 μg m⁻³ and at Delhi were 126.7 ± 28.6, 268.6 ± 39.1, and 687.7 ± 117.4 μg m⁻³. Values at Delhi were well above the standard limit for 24-h PM_2.5 United States National Ambient Air Quality Standards (USNAAQS; 65 μg m⁻³), while values at Satna were under the standard limit. Results were compared with various worldwide studies. These comparisons suggest an immediate need for the promulgation of new PM_2.5 standards. The position of PM₁₀ in Delhi is drastic and needs an immediate attention. PM₁₀ levels at Delhi were also well above the standard limit for 24-h PM₁₀ National Ambient Air Quality Standards (NAAQS; 150 μg m⁻³), while levels at Satna remained under the standard limit. PM_2.5/PM₁₀ values were also calculated to determine PM_2.5 contribution. At Satna, PM_2.5 contribution to PM₁₀ was only 20% compared to 47% in Delhi. TSP values at Delhi were well above, while TSP values at Satna were under, the standard limit for 24-h TSP NAAQS (500 μg m⁻³). At Satna, the PM₁₀ contribution to TSP was only 26% compared to 39% in Delhi. The correlation between PM₁₀, PM_2.5, and TSP were also calculated in order to gain an insight to their sources. Both in Satna and in Delhi, none of the sources was dominant a varied pattern of emissions was obtained, showing the presence of heterogeneous emission density and that nonrespirable suspended particulate (NRSP) formed the greatest part of the particulate load.