Air Quality Status of an Open Pit Mining Area in India

This investigation presents the assessment of ambient air quality carried out at an open pit coal mining area in Orissa state of India. The 24-h average concentrations of suspended particulate matter (SPM), respirable particulate matter (RPM, particles of less than 10 m aerodynamic diameter), sulphur dioxide (SO₂) and oxides of nitrogen (NO_x) were determined at regular interval throughout one year at 13 monitoring stations in residential area and four stations in mining/industrial area. During the study period, the 24-h and annual average SPM and RPM concentrations exceeded the respective standards set in the Indian ambient air quality standard (NAAQS) protocol in most of the residential and industrial areas. However, the 24-h and annual average concentrations of SO₂ and NO_x were well within the prescribed limit of the NAAQS in both residential and industrial areas. A management strategy is formulated for effective control of particulate matter at source and other mitigative measures are recommended including implementation of green belts around the sensitive areas.     

Monitoring of Daily Integrated Exposure of Outdoor Workers to Respirable Particulate Matter in an Urban Region of India

It is more and more recognised that an estimation of the exposure of the population to air pollutants is more relevant than the ambient air quality, since it gives a better indication of health risk. Outdoor workers in an urban region are generally of low income status and are exposed to higher levels of both indoor and outdoor air pollution. Hence respondents from this population subgroup have been selected for this study. Outdoor workers are divided into two categories, viz. traffic constables and casual outdoor workers like watchmen, roadside shopkeepers etc. Most of the respondents are from the lower income group. Each respondent is monitored for a continuous 48-hour period. The sampling frequency is once a week.The study region is situated in the north-west part of the Greater Mumbai Municipal Corporation. It can be classified as industrial cum residential area. The daily integrated exposure of the outdoor workers consists of two major micro-environments, viz. occupational and indoor residential.A personal air sampler was used along with a cyclone to measure levels of Respirable Particulate Matter (RPM). The cyclone has a 50% removal efficiency for particle diameter of 5 m. Paired samples of PM10 (ambient) and RPM (personal) were collected to establish the correlation between them. The average 24-hour integrated exposure to RPM was 322 g/m3 and exceeded the corresponding PM10 level observed at the nearest Ambient Air Quality Monitoring Station by a factor of 2.25. The 90% confidence interval for this exposure is 283–368 g/m3. This study clearly demonstrates that the daily integrated exposure and therefore the health risk of outdoor workers in an urban area is significantly more serious than that indicated by ambient air quality data.     

Exposure estimates in assessing helath effects of air pollution

Air pollution has been associated with adverse health effects. Difficulties in interpreting studies of health effects of exposure to air pollution arise in estimating exposure. Until recently, studies of effects of air pollution have relied on pollution exposure measurements obtained from fixed location air pollution stations monitoring outside air (to evaluate compliance with air quality standards, rather than to examine population exposure). However, recent evidence suggests that there are substantial differences between air pollution levels measured at such sites and levels to which people are actually exposed, i.e. personal exposure. The present study examines effects of ambient urban air pollution on persons suffering from asthma, healthy non-asthmatic subjects and school children (in 2 Canadian cities, Toronto and Hamilton). Air pollution exposure is being assessed by data obtained from: (1) conventional abatement oriented fixed location air pollution monitoring stations, (2) an extensive population oriented network, (3) inside and (4) outside structures (homes and schools) as well as (5) personal air pollution samplers. The data indicate variability in these different estimates of exposure which have implications on health effects assessment.     

Correlation between environmental parameters and leaf injury in Nicotiana tabacum L. cv. ‘Bel-W 3’

Tobacco plants (Nicotiana tabacum L. cv. Bel-W3) were exposed to ambient air for 25 weeks during the 1987 growing season next to an air pollution monitoring station in Brera (Milan, Italy). The research objective was to study the influence of selected environmental parameters on leaf damage in this plant, which is widely used as an ozone indicator. A multiple linear correlation model was estimated between leaf damage and available meteorological and air pollution data. Leaf injury was positively correlated with ozone integrated exposure and temperature, but negatively with vapour pressure deficit. A linear correlation model was used to estimate ozone integrated exposure from the leaf injury indexWork carried out as part of the research programme: ENEL's contribution to the knowledge of important environmental issues, research line: Effects of atmospheric pollution on the land.     

Measurements of Ozone Concentrations in Zagreb

Ozone concentrations were measured in Zagreb at four sites from May 1999 to April 2001 in order to categorize the air quality with respect to ozone. In the summer of 2000, the ozone measurements were also extended to four sites in the suburbs of Zagreb. Methods of active and passive sampling with nitrite ion as a reagent were used. In the northern part of the town ozone was analyzed by an automatic device. Automatic device measurements in the years 1999 and 2000 showed that hourly averages of ozone concentrations did not exceed the Croatian recommended value of the 98th percentile (180 g m^–3). Over the two-year period, 24-h averages occasionally exceed 110 g m^–3 in city center and in the northern part of the town. Regardless of these isolated examples, ozone was well within acceptable concentrations. Ozone concentrations measured in summer 2000 were higher in the suburbs of Zagreb than in the city. The 98th percentile values higher than 110 g m^–3 were recorded at three sites.     

Atmospheric Volatile Organic Compound Monitoring. Ozone Induced Artefact Formation

Assessment of population exposure to VOC in ambient atmospheres is receiving heightened interest as the adverse health effects of chronic exposure to certain of these compounds are identified. Active (pumped) and passive samplers are the most commonly used devices for this type of monitoring. It has been shown, however, that these devices, along with all other preconcentration techniques, are susceptible to ozone interference. It is demonstrated that this interference occurs even at low ozone concentrations and that it may result in the under-estimation of population exposure. A convenient and effective ozone scrubbing method is identified and successfully applied and validated for both active and passive samplers for a range of VOC.     

Forecasting Daily Maximum Ozone Concentrations in the Athens Basin

In the work ozone data from the Liossion monitoring station of the Athens/PERPA network are analysed. Data cover the months May to September for the period 1987–93. Four statistical models, three multiple regression and one ARIMA (0,1,2), for the prediction of the daily maximum 1-hour ozone concentrations are developed. All models together, with a persistence forecast, are evaluated and compared with the 1993's data, not used in the models development. Validation statistics were used to assess the relative accuracy of models. Analysis, concerning the models' ability to forecast real ozone episodes, was also carried out. Two of the three regression models provide the most accurate forecasts. The ARIMA model had the worst performance, even lower than the persistence one. The forecast skill of a bivariate wind speed and persistence based regression model for ozone episode days was found to be quite satisfactory, with a detection rate of 73% and 60% for O3 >180 g m-3 and O3 >200 g m-3, respectively.     

对进口TSP大流量采样器控制电路的改进

在空气质量自动监测系统中,ＴＳＰ大流量采样器长年安装在各子站,无人值守。由于各种原因,有时出现不该采样时的误启动,从而降低了仪器的使用寿命。为此对其电路进行了改善。改进了可控硅电路,加装了自锁电路,使仪器在没有采样膜时自行锁定不运转,延长了仪器的使用寿命。     

Monitoring Air Quality in Mountains: Designing an Effective Network

A quantitatively robust yet parsimonious air-quality monitoring network in mountainous regions requires special attention to relevant spatial and temporal scales of measurement and inference. The design of monitoring networks should focus on the objectives required by public agencies, namely: 1) determine if some threshold has been exceeded (e.g., for regulatory purposes), and 2) identify spatial patterns and temporal trends (e.g., to protect natural resources). A short-term, multi-scale assessment to quantify spatial variability in air quality is a valuable asset in designing a network, in conjunction with an evaluation of existing data and simulation-model output. A recent assessment in Washington state (USA) quantified spatial variability in tropospheric ozone distribution ranging from a single watershed to the western third of the state. Spatial and temporal coherence in ozone exposure modified by predictable elevational relationships ( 1.3 ppbv ozone per 100 m elevation gain) extends from urban areas to the crest of the Cascade Range. This suggests that a sparse network of permanent analyzers is sufficient at all spatial scales, with the option of periodic intensive measurements to validate network design. It is imperative that agencies cooperate in the design of monitoring networks in mountainous regions to optimize data collection and financial efficiencies.     

Toxicity of a complex mixture of atmospherically transported pesticides to Ceriodaphnia dubia

The presence of several anthropogenic chemicals has been documented in the atmosphere of the Canadian prairies. The deposition of these chemicals as a mixture is of importancesince little is known of the combined effects of these chemicalson aquatic organisms. This study was designed to evaluate theacute and chronic toxicity of a complex mixture of nineatmospherically transported pesticides to Ceriodaphniadubia. The nine selected pesticides (bromoxynil, dicamba, 2,4-D,MCPA, triallate, trifluralin, pentachlorophenol, lindane, and4,4-DDT) were detected in appreciable quantities in dryatmospheric deposits. The concentration of each pesticide in themixture was based on maximum measured daily dry deposition ratesfor central Canada, except for pentachlorophenol, which wasestimated based on atmospheric concentrations. The 48-h LC50estimate for C. dubia exposed to the pesticide mixture was174.60 g L^-1 (340 times the measured total dry deposition concentration). The estimated NOEC and LOEC for bothsurvival and reproduction, as determined in the 7-d chronic toxicity test, were 51.3 (100 times) and 154 g L^-1 (300 times), respectively. A basic risk assessment, using the toxic unit approach, suggested that the toxicity of the pesticide mixture was mainly due to 4,4-DDT. Overall, this atmospherically transported complex mixture of pesticides appearsto pose a negligible toxicological risk to non-target aquatic invertebrates such as zooplankton.     

Roadside Concentration of Gaseous and Particulate Matter Pollutants and Risk Assessment in Dar-Es-Salaam, Tanzania

This study used manual air sampling method to assess the contribution of road traffic to air pollution level in Dar-es-Salaam City, Tanzania. Samples were collected from 11 different sites. Parameters measured were: sulphur dioxide using pararosaniline method, nitrogen dioxide using saltzman method, particulate matter and particulate lead using filtration method and atomic absorption spectrometric method, respectively. Results showed that hourly average sulphur dioxide concentration range from 127 to 1385 g/m³. The measured values of sulphur dioxide were above the recommended WHO guidelines with an hourly objective value of 350 g/m³ at 87% of the sampling sites. The hourly average nitrogen dioxide concentration ranged from 18 to 53 g/m³. The maximum hourly nitrogen dioxide concentration at 53 g/m³ was below the WHO guideline value of 200 g/m³. The hourly average suspended particulate matter (SPM) ranged from 98 to 1161 g/m³, exceeding the recommended value of 230 g/m³ by WHO at 87% of the sampling sites. The hourly average lead concentration was found to range from 0.60 to 25.6 g/m³, exceeding again the WHO guideline value of 1.5 g/m³at 83% of the sampling sites. Results predicted by Gaussian model when compared with the measured values were found to have a correlation coefficient of 0.8, signifying a good correlation. The risk assessment was undertaken considering the people who spend a significant portion of their time near the roads, such as the Uhuru primary school pupils and the adult population who reside by the roadside. The unit risk realised was 18.2 × 10^–6 for adult population and 2.2 × 10^–6 for pupils, both scenarios showing risk higher than the United Sates of America Environmental Protection Agency (USEPA) acceptable limit of 1× 10^–6. Considering the magnitude of the problem at hand, this study recommends an introduction of mandatory emission tests of SPM, lead and sulphur dioxide (SO₂). The study further recommends the introduction of continuous and/or regular air quality monitoring and the use non-leaded petrol in Tanzania.     

Particulate emission inventory and trends in ambient particulate matter concentrations in the Czech Republic between 1993 and 1999

Trends in total suspended particulates (TSP) emissioninventories were compared with ambient TSP concentrationsduring the period of 1993-1999 in the Czech Republic. TheTSP annual emission decreased within the period of observationfrom 441 300 to 67 000 of metric tonnes (by 85%). During thesame period a less pronounced downward trend from80.3 g m^-3 to 31.5g m^-3 (decrease by 61%)was noted also for the ambient TSP annual average. Differencebetween the two air quality indicators seems to indicate thatchanges in TSP emission inventories from year to year arebeing to some extent overestimated. Monthly ambientparticulate concentrations did not respond to overall drop inemissions proportionately but were closely associated withmonthly mean temperatures. While in the winter the correlationbetween ambient TSP and temperature was negative, in summerthe correlation between the two variables was positive. Inspring and autumn there was no clear correlation betweentemperature and ambient particulate pollution. The improvementof air quality in the Czech Republic since the economical andpolitical transformation in 1990s is substantial whendemonstrated by emission figures, however, true state ofparticulate pollution expressed by ambient levels requiresfurther attention.     

PM2.5 and PM10 Concentrations from the Qalabotjha Low-Smoke Fuels Macro-Scale Experiment in South Africa

This article presents results from the particulate monitoringcampaign conducted at Qalabotjha in South Africa during the winter of 1997. Combustion of D-grade domestic coal and low-smoke fuels were compared in a residential neighborhood to evaluate the extent of air quality improvement by switchinghousehold cooking and heating fuels.Comparisons are drawn between the gravimetric results from the two types of filter substrates (Teflon-membrane and quartz-fiber) as well as between the integrated and continuous samplers. It is demonstrated that the quartz-fiber filters reported 5 to 10% greater particulate mass than the Teflon-membrane filters, mainly due to the adsorption of organic gases onto the quartz-fiber filters. Due to heating of sampling stream to 50 °C in the TEOM continuous sampler and the high volatile content of the samples, approximately 15% of the particulate mass was lost during sampling.The USEPA 24-hr PM_2.5 and PM₁₀ National Ambient Air Quality Standards (NAAQS) of 65 g m^-3 and 150 g m^-3, respectively, were exceeded on several occasions during the 30-day field campaign. Average PMconcentrations are highest when D-grade domestic coal was used, and lowest between day 11 and day 20 of the experiment when a majority of the low-smoke fuels were phased in. Source impacts from residential coal combustion are also found to be influenced by changes in meteorology, especially wind velocity.PM_2.5 and PM₁₀ mass, elements, water-soluble cations (sodium, potassium, and ammonium), anions (chloride, nitrate, and sulfate), as well as organic and elemental carbonwere measured on 15 selected days during the field campaign. PM_2.5 constituted more than 85% of PM₁₀ at three Qalabotjha residential sites, and more than 70% of PM₁₀ at the gradient site in the adjacent community of Villiers. Carbonaceous aerosol is by far the most abundant component, accounting for more than half of PM mass at the three Qalabotjha sites, and for more than a third of PM mass at the gradient site. Secondary aerosols such as sulfate, nitrate,and ammonium are also significant, constituting 8 to 12% of PM mass at the three Qalabotjha sites and 15 to 20% at the Villiers gradient site.     

Environmental Assessment of the Impact of Ozone to the Neuston of the Sea-Surface Microlayer of the Gulf of Mexico

Substantial amounts of NOx (146 000 t/y) and total hydrocarbons (294 000 t/y) are released to the marine atmosphere by the large number of oil and gas operations over Federal waters of the Gulf of Mexico (GOM). Under appropriate meteorological conditions these emissions react to form ozone (0–54 g/m3 over-water) which can affect the marine environment. Using a dry deposition model, this work examines the amount of ozone derived from oil and gas offshore operations and deposited in the sea surface of the Gulf of Mexico, and assesses its impact on the neuston of the sea-surface microlayer. Surface integrated estimates of ozone deposited from oil and gas operations over the sea surface ranges from 400 kg to 1800 kg which results in sea surface concentrations of 15 g/m3. This estimate and the actual toxic ozone levels suggest no acute, toxic impacts to the neuston. However, indirect effects may occur through changes to the pelagic foodwebs and organic carbon pathways. Another potential pathway for ozone impacting the environment is through the production of bromate. Based on the concentrations and time scales (11–139 days) only sublethal effects appear to occur, but uncertainties associated with this assessment need to be further studied. From an ecological perspective, the environmental impacts and risks of NOx and VOC discharges from offshore platforms need to be assessed for neuston and other components of the marine ecosystem.     

Errors in ozone risk assessment using standard conditions for converting ozone concentrations obtained by passive samplers in mountain regions

Passive samplers are often employed to measure ozone concentrations in remote areas such as mountain forests. The potential ozone risk for vegetation is then assessed by calculating the AOT40 exposure index (accumulated hourly ozone concentration exceedances above 40 ppb, i.e. AOT40 = Σ([O(3)] - 40)Δt for any hourly ozone concentration [O(3)] > 40 ppb). AOT40 is customary calculated on the basis of ozone concentrations expressed as a volumetric mixing ratio, while lab sheets normally report ozone concentrations from passive samplers in mass units per cubic metre. Concentrations are usually converted from mass units to ppb using a standard conversion factor taking SATP (Standard Ambient Temperature and Pressure) conditions into account. These conditions, however, can vary considerably with elevation. As a consequence, the blanket application of a standard conversion factor may lead to substantial errors in reporting and mapping ozone concentrations and therefore in assessing potential ozone risk in mountain regions. In this paper we carry out a sensitivity analysis of the effects of uncertainties in estimations of air temperature (T) and atmospheric pressure (P) on the concentration conversion factor, and present two examples from two monitoring and mapping exercises carried out in the Italian Alps. We derived P and T at each site from adiabatic lapse rates for temperature and pressure and analysed the magnitude of error in concentration estimations. Results show that the concentration conversion is much more sensitive to uncertainties in P gradient estimation than to air temperature errors. The concentration conversion factor (cf) deviates 5% from the standard transformation at an elevation of 500 m asl. As a consequence, the standard estimated AOT40 at this elevation is about 13% less than the actual value. AOT40 was found to be underestimated by an average between 25% and 34% at typical elevations of mountain forest stands in the Italian Alps when a correct conversion factor for transforming ozone concentrations from μg m(-3) to ppb is not applied.     

Monitoring and biomonitoring of surface ozone in Florence, Italy

An ambient air study was conducted inthe city of Florence, Italy, in the summer 1996.Tropospheric ozone was continuously monitored withautomatic analyzers in three stations, two located inthe urban area and one in the hilly surroundings(Settignano). A biomonitoring campaign based on thetobacco cv. Bel-W3 plants was performed in the samearea. The highest values were constantly recorded inthe Settignano station. The highest 1-hour meanrecorded was 197 nl/l; the accumulated exposure overa threshold of 40 nl/l (AOT40) was well above thecritical levels standards for protection of thevegetation. A consistent temporal variation wasobserved and July proved to be the month with thehighest ozone levels. Cumulative frequencydistribution of ozone maximum daily concentrationsexhibited a good fitting to log-normality. No`week-end effect was observed. Biomonitoring datawere in good agreement with chemico-physical ones.     

SMOKE CONCENTRATION AS AN INDICATOR OF POLYCYCLIC AROMATIC HYDROCARBONS LEVELS IN THE AIR

The relationship of polycyclic aromatichydrocarbons (PAH) and smoke concentrationwas analysed at four different locations in Zagreb during theheating season. At two sampling sitessmoke pollution came primarily from domestic heating while theother two sites were under a directinfluence of traffic. At locations away from trafficcorrelations between smoke and PAH concentrationswere stochastically significant at 0.01 level. Takingbenzo-a-pyrene (BaP) as a PAH representative itwas shown that for these two locations the smoke/BaPrelationship can be presented with a singleregression line which can serve for rough assessment of BaPlevels in the air. The BaP concentrationof 10 ng/m³ – proposed by the German FederalEnvironmental Agency as orientation < mark (Lahman et al., 1984) – might be expected to occurat smoke levels 60 g/m³,and above this level it is recommended to start measuringactual concentrations of PAH.     

Measurement of atmospheric concentrations of common household pesticides: A pilot study

Air concentrations of 28 of the most commonly used household pesticides were measured inside nine homes in Jacksonville, Florida, and compared with corresponding outdoor levels. The households selected were sorted into three categories according to the degree of pesticide indoor usage. Personal air monitoring was also performed on one resident of each household by means of a portable sampler, which was kept with the person at all times. Five of the pesticides were found in the air inside of the majority of the homes at concentrations as high as 15 gm^–3 (average concentrations, 12 ngm^–3 to 2.4 gm^–3). Indoor levels were generally one to two ordrrs of magnitude higher than surrounding outdoor air levels and personal air measurements were within ± 50% of corresponding indoor values. All samples were collected over 24-hr periods on polyurethane foam and analyzed by capillary colum gas chromatography with mass spectrometric and/or electron capture detection.     

Intake of Chromium by the Adult Population of Mumbai City

Electro Thermal Atomic Absorption Spectrophotometry (ET-AAS), is used for the determination of chromium (Cr) in a variety of environmental matrices. The detection limit for the estimation of Cr is 2 pg absolute for a volume injection of 20 l. The precision of the method is established by analysing Cr from a synthetic mixture containing various elements in different qualities (0.5–10 ppm) and is found to be within ± 8%. The reliability of estimation is further assessed through the analysis of Standard Reference Materials (SRMs) of soil, hay, milk powder and lake sediment obtained from IAEA.The total intake of Cr through air, water and food works out to be 54 g/day for the adult population of Mumbai city. The dietary intake through food is the major contributor to the total intake of Cr. The concentration of Cr in atmospheric air and drinking water collected from different suburbs showed geometric mean concentrations of 0.09 g/m³ and 0.3 g/l, respectively. The daily intake of Cr, though lower, is closer to the lower bound of the recommended value of 50–200 g/day.     

Mercury Vapor Determination in Hospitals

The measurements of metallic mercury vapor were carried out in seven local hospitals, where mercury-containing products are widely used, as well as in one residence to check effectiveness of decontamination after mercury spillage. Hopcalite as a solid sorbent was used in active and passive sampling methods, and mercury was analyzed by CV-AAS technique. Good agreement was found between results of mercury measurements using active samplers (pumped hopcalite adsorption tubes) and passive (diffusion) monitors applied in indoor atmosphere. The results indicated the presence of metallic mercury vaporization sources in the assessed hospital rooms but in the majority of cases mercury levels did not exceed 1 g/m³ i.e. Polish permissible concentration for residence. However, in some of the hospital rooms, elevated concentrations of mercury vapor were found and airborne levels of up to 13.9 g/m³ were recorded. Higher concentrations of mercury vapor were observed in autumn season when compared to summer.