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.     

Heavy Metal Concentrations in and Around Households Near a Secondary Lead Smelter

Housedusts and garden soils were sampled in 14 houses in the vicinity of a secondary Pb smelter and analysed for concentrations of Pb, Zn, Cu, Cd, As, and Hg. Sixty-one topsoil samples were also taken from a 2 km² grid covering the smelter grounds and surrounding residential areas and analysed for concentrations of Pb, Zn, Cd and Cu. Contour maps generated from the grid data indicate significant contamination in the area (maximum Pb concentration 58 500 g g^-1), particularly down-wind of the smelter grounds. A geometric mean Pb concentration of 2225 g g^-1 was recorded in garden soil and similarly elevated levels were recorded for Zn, Cd, As and Sb. In housedusts, a geometric mean Pb concentration of 1668 g g^-1 was observed. Whilst housedust metal concentrations were generally elevated, compared to other urban or residential areas, there appears to be a large degree of attenuation of the metals between the exterior and interior environments of the homes studied. A significant correlation was not recorded between metal concentrations of garden soils and housedusts. There were significant correlations for: distance from the smelter against garden soil metal concentrations; garden soil metal concentrations against each other; housedust metal concentrations against each other; and house age against garden soil metal concentrations.     

Performances and application of a passive sampling method for the simultaneous determination of nitrogen dioxide and sulfur dioxide in ambient air

The performances and applicability of a diffusion tubesampler for the simultaneous measurements of NO₂ andSO₂ in ambient air were evaluated. SO₂ andNO₂are collected by the passive sampler using triethanolamine astrapping agent and are determined as sulphate and nitrite withion chromatography. The detection limit (2.3 g m^-3 ofNO₂ and 4.2 g m^-3 of SO₂ for two weekssampling) is adequate for the determination of concentrationsin urban and industrial areas. Precision of the method as RSDis in mean 5% for NO₂ and 12% for SO₂ at theconcentration levels in urban areas. Calibration of the methodwas performed in the field conditions by comparison between theresponses of sampler and the concentrations measured by thecontinuous monitors. High degree of linearity (correlationcoefficients > 0.8) is found between the passive sampler tubeand the continuous monitor data for both NO₂ and SO₂.To reduce the wind velocity influence on passive sampling ofdiffusion tubes, a protective shelter was tested in this study.The overall uncertainty of one measure for the optimised methodis estimated at 5 g m^-3 for NO₂ and 6g m^-3 for SO₂. Suitability of this passivesampling method for air pollution monitoring in urban areas wasdemonstrated by the results shown in this paper on a campaigncarried out in the French agglomeration.     

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.     

COMBUSTIVE APPROACH FOR MEASURING TOTAL VOLATILE PHOSPHORUS CONTENT IN LANDFILL GAS

A technique was developed to measure the total gaseous phosphorus content in biogas. The amount of air needed for a neutral to oxidising flame was mixed with the biogas. The gas mixture was burnt in a closed quartz burner and the combustion gasses were bubbled through a nitric acid solution. The phosphate content in the bubbling liquid was determined with sector field ICP-MS. The technique was validated in the lab with phosphine. Afterwards the set-up was installed on a landfill. The total gaseous phosphorus content in the landfill gas, measured with the combustive technique, ranged from 1.65 to 4.44 g P/m³. At the same time the phosphine concentration in the landfill gas was determined gas chromatographically (GC). The phosphine (PH₃) content measured with GC ranged from 7.6 to 16.7 g PH₃-P/m³. Since the phosphine-P content (GC) was consistently higher than the total gaseous phosphorus content (burner/ICP-MS), the hypothesised presence of highly toxic gaseous phosphorus compounds other than phosphine could not be demonstrated.     

A Survey of Trace Metals in Vegetation, Soil and Lower Animal Along Some Selected Major Roads in Metropolitan City of Lagos

The concentration of trace metals (Cd, Cu, Pb and Zn) in a total of 144 samples of grass, soil and lower animal (earthworm, Lybrodrilus violaceous) were collected and analysed for their metallic content. Levels of cadmium ranged from 0.01–0.07 g g^–1; 0.01–0.12 g g^–1 and from trace–0.05 g g^–1 dry weight for plant, soil and animal samples respectively. Mean concentration of copper ranged 0.10–1.48 g g^–1; 0.10–2.90 g g^–1 and 0.01–0.08 g g^–1 for samples in similar order as above. The levels of Pb varied from 0.01–0.14 g g^–1; 0.02–0.23 g g^–1 and from trace–0.07 g g^–1 while that of Zn ranged from 0.19–1.80 g g^–1; 0.51–3.35 g g^–1and 0.01–0.08 g g^–1 also in the same order of samples as mentioned above. Levels of metals in soil samples were higher than the background levels with the exception of Zn but lower than European Union (EU) limits. The results generally revealed the presence of metals in plant and animal samples and metal dynamics up the food chain is highly possible. Acceptable recoveries of the spiking experiment validate the experimental protocol.     

Ambient Air Quality Status in Raniganj-Asansol Area, India

This investigation presents the assessment of ambient air quality with respect to suspended particulate matter (SPM), sulphur dioxide (SO₂) and oxides of nitrogen (NO_X) at four sites (RGC, SRS, BBC and BCC) in the Raniganj-Asansol area in West Bengal, India. Ambient air was monitored with a sampling frequency of twenty four hours (3 × 8 hours) at each site on every alternate day (3 days a week) covering a period of one year. A total of 429 samples were collected from RGC, 429 from SRS and 435 each from the BBC and BCC sites. Meteorological parameters such as temperature, relative humidity, wind-speed and wind-direction were also recorded simultaneously during the sampling period. Monthly and seasonal variation of these pollutants have been observed and recorded. The annual average and range values have also been calculated. Results of the investigation indicates that the 95th percentile values of SPM levels exceed the limits (200 g m^-3) at RGC, SRS and BBC sites and is within the limit of 500 g m^-3 at the BCC sites. The 95th percentile values of SO₂ levels did not exceed the reference level at any of the monitoring stations. The 95th percentile values of NO_X are found to be exceeding the limit (80 g m^-3) at RGC, SRS and BBC sites but is within the prescribed limit of 120 g m^-3 at the BCC site. Further, it has been observed that the concentrations of the pollutants are high in winter in comparison to the summer or the monsoon seasons. Results of the investigation indicates that industrial activities, indiscriminate open air burning of coal by the local inhabitants for cooking as well as coking purposes, vehicular traffic, etc. are responsible for the high concentration of pollutants in this area.     

Trihalomethane Formation Potential and Concentration Changes During Water Treatment at Mumbai (India)

The treated water at the outlet oftreatment plants and representative servicereservoirs of Mumbai city have been evaluatedfor trihalomethane formation potential in1995–1996. Chloroform, dichlorobromomethane,chlorodibromomethane and bromoform have beenmonitored during monsoon, winter and summer.The levels of chloroform are found above theregulated WHO guideline value of 200 g L^-1 in final water during postmonsoon atGhatkopar (226 g L^-1), Malbar (210.3 g L^-1) and Tulsi (231.26 g L^-1).     

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.     

Aldehyde Concentrations in Ambient Air of Coastal Georgia, U.S.A.

Aldehydes are an airborne byproduct of many industrialprocesses, vehicle transportation, and emissions fromnumerous natural sources. To characterize aldehydeconcentrations in ambient air of the Savannah, Georgiaarea, air samples for 3 aldehydes (formaldehyde,acetaldehyde, and propionaldehyde) were collected atfive sites on a monthly basis over a 12-month periodfrom December of 1995 through November 1996. Four ofthe sites were in central Savannah and the fifth sitewas located in a rural area about 56 km south ofSavannah. During each 24-hr sampling episode, sampleswere collected in two 12-hr periods approximatingdaylight and nighttime hours, following U.S. EPAMethod TO-11. Formaldehyde concentrations ranged from0.17 to 6.80 g m^-3, acetaldehydeconcentrations ranged from 0.07 to7.60 g m^-3, and propionaldehyde levels rangedfrom 0.02 to 9.10 g m^-3. On average, thefour sites in Savannah had higher aldehydeconcentrations than the rural site (2.0 versus1.2 g m^-3 for formaldehyde, 2.3 versus1.7 g m^-3 for acetaldehyde, and 1.2 versus1.0 g m^-3 for propionaldehyde). The daytimeconcentrations for formaldehyde and acetaldehyde werehigher than the nighttime levels. The data from allthe sites were within published worldwide backgroundvalues for aldehydes.     

Characterization of atmospheric dust at Gurushikar,Mt. Abu,Rajasthan

The nature of atmospheric aerosols at Gurushikar, Mt. Abu, Rajasthan where a gamma ray telescope is to be installed, was investigated. Air particulate samples collected on filters were used to estimate the total suspended particulate matter (TSPM) and its elemental composition. The TSPM varied from 31 to 103 g/m³ during January to March 1994. The heighest loads were observed during the months of May and June (80–100 g/m³) and lowest during October (20–60 g/m³). The dust was also examined for size, shape and nature of the mineral matter. The particle sizes varied from 100 m to 5 m. The course particles (>50 m) are irregular shaped quartz grains. Some of the medium size (=50 m) particles were spherical and were highly conducting. These particles were rich in iron content. Correlation coefficients among various elements in the dust showed that it is made up of mainly two components-wind blown ground dust and particulate arising out of wood and coal burning.     

Environmental monitoring of carbaryl applied in urban areas to control the glassy-winged sharpshooter in California

Carbaryl insecticide was applied by ground spray to plants in urban areas to control a serious insect pest the glassy-winged sharpshooter, Homalodisca coagulata (Say), newly introduced inCalifornia. To assure there are no adverse impacts to human health and the environment from the carbaryl applications, carbaryl was monitored in tank mixtures, air, surface water, foliage and backyard fruits and vegetables.Results from the five urban areas – Porterville, Fresno, Rancho Cordova, Brentwood and Chico – showed there were no significanthuman exposures or impacts on the environment. Spray tank concentrations ranged from 0.1–0.32%. Carbaryl concentrationsin air ranged from none detected to 1.12 g m^-3, well below the interim health screening level in air of 51.7 g m^-3. There were three detections of carbaryl in surface water nearapplication sites: 0.125 ppb (parts per billion) from a water treatment basin; 6.94 ppb from a gold fish pond; and 1737 ppbin a rain runoff sample collected from a drain adjacent to a sprayed site. The foliar dislodgeable residues ranged from 1.54–7.12 g cm^-2, comparable to levels reported forsafe reentry of 2.4 to 5.6 g cm^-2 for citrus. Carbarylconcentrations in fruits and vegetables ranged from no detectableamounts to 7.56 ppm, which were below the U.S.EPA tolerance, allowable residue of 10 ppm.     

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.     

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.     

Effect of Common Pesticides Used in the Niger Delta Basin of Southern Nigeria on Soil Microbial Populations

The effects of eleven pesticides on the populations of bacteria, actinomycetes, fungi and protozoa was investigated by treating a garden soil with their recommended rates. The microbial populations were estimated using the standard plate-count technique. Of the ll pesticides investigated, phenylmercuric acetate (agrosan) at 50 g g^-1 inhibited bacterial density the most, i.e. from 4,600,000 to 220 cells g^-1. The pesticides were Pentachloronitrobenzene (PCNB), tetramethylmethylthiuram disulphide (thiram),1- naphthylmethylcarbamate (Vetox 85), 1,2,3,4,5,6-hexachlorocyclohexane (Gammalin 20), phenylmercuric acetate (Agrosan), tetrachloroterephthalic acid (Dacthal), 4-nitrophenyl –2-nitro-4-trifluoromethylphenyl ether (Preforan), 2-ethyl-6-methyl –N-2-methoxy –1-methyl ethyl-chloroacetanide (Dual), Benlate, Brestan and Gramoxone. Pentachloronitrobenzene (PCNB) at 240,000 g g^-1 reduced bacterial population from 4,600,000 to 2,100 cells g^-1, whereas tetramethylthiuram disulphide (thiram) at 100 g g^-1 suppressed it by 2 log orders of magnitude. Soil application of 1-naphthylmethylcarbamate (Vetox 85) at 100 g g^-1 and 1,2,3,4,5,6,-hexachlorocyclohexane (Gamalin 20) at 1,300 g g^-1 repressed the bacterial numbers by 2 log orders of magnitude each. Pentachloronitrobenzene reduced the actinomycetes density from 340,000 to 320 cells g^-1 and completely eliminated all fungal and protozoan propagules from the soil. The Gammalin 20 completely wiped out all the fungi, whereas phenylmercuric acetate totally eliminated all the protozoa and reduced the fungal population from 34,000 to 60 cells g^-1. In general, protozoa and fungi were more susceptible to fungicides than bacteria and actinomycetes. Pentachloronitrobenzene, 1,2,3,4,5,6,-hexachlorocyclohexane and phenylmercuric acetate were toxic particularly to soil microorganisms, whereas the herbicides dacthal, Preforan and Dual were quite harmless in soil at application rates of 0.1, 0.06 and 0.02 g g^-1 respectively.     

Arsenic uptake and loss in the American oyster,Crassostrea virginica

In addition to a control Crassostrea virginica was treated with 3 and 5 g As kg^p-1 for 16 wks at ambient seawater salinity and temperature to determine the potential of C. virginica as an indicator of arsenic pollution. Prior to spawning, as much as 10.3±1.5, 12.7±2.7, and 14.1±3.7 g As g^p-1 dry weight were accumulated in the total soft parts of oysters after treatment with ambient (control), 3 and 5 g As kg^-1, respectively. Immediately after spawning, an increase in tissue arsenic concentration was observed in all treatments up to week 12, after which a decrease in tissue arsenic concentrations occurred despite continuous addition of arsenic to the seawater. During the uptake period, a significant inverse relationship existed between dry weight and tissue arsenic concentration, whereas a significant direct relationship was apparent between dry weight and tissue content. Arsenic concentration in the total soft parts is not significantly related to seawater arsenic concentration over the range of concentrations used in this study. In all three treatments, arsenic uptake as concentration (g g^p-1) is not a significant linear function of time. Weight loss was significant but gradual during the first 16 wks of treatment and did not change significantly during the depuration period (wks 17–25). Tissue arsenic concentrations increased significantly in oysters from all three treatments during the depuration period. Generally, arsenic body burdens increased with increases in phytoplankton concentration and it appears that food contributes more to arsenic uptake than seawater arsenic concentrations. Since a relationship between tissue arsenic concentration and seawater arsenic concentration does not appear to exist, C. virginica would not be a good biological indicator of arsenic concentration in its environment.     

Atmospheric Dust Loads and Their Elemental Composition at a Background Site in India

Air particulate samples collected during 1995–96 ata background site situated on the east coast of Thar Desert inRajsthan State of India were analysed for atmospheric dustloads (Suspended Particulate Matter) and elemental composition.The values of SPM ranged from 9 g M^-3 to 97g M^-3 with an average of 43 g M^-3 except a fewepisodic values, which were 3 to 5 times higher than the averageduring summer months. The results for elemental composition ofthe particulate samples showed that the concentrations ofanthropogenic toxic trace elements viz. Br, Cr, Pb, Sb, Se and Znare lower by a factor of 2 to 10 as compared to urban areas. Thehigh enrichment factors for anthropogenic elements viz. Br, Pb,Sb and Zn show an input from coal/wood fuel burning andvehicular pollution at the sampling site. The depletion of Si inSPM samples shows long distance transport of dust to the samplingsite.     

Comparability between PM2.5 and particle light scattering measurements

Particle light scattering and PM_2.5 (particles with aerodynamic diameters less than 2.5 m) concentration data from air quality studies conducted over the past ten years wereexamined. Fine particle scattering efficiencies were determinedfrom statistical relationships among measured light scattering and fine and coarse mass concentrations. The resulting fine particle scattering efficiencies ranged from 1.7 m² g^-1at Meadview in the Grand Canyon to over 5 m² g^-1 in Mexico City. Most of the derived fine scattering efficiencieswere centered around 2 m² g^-1, which is considerablylower than most values reported from previous studies.     

Characterisation of particulate matter emissions from the Zimbabwe Mining and Smelting Company (ZIMASCO) Kwekwe Division (Zimbabwe): a ferrochrome smelter

Particulate matter emissions from stack number 2 of a majorferrochrome smelter, Zimbabwe Mining and Smelting Company(ZIMASCO) were characterized and the rates at which the elementsCr, Fe, Cu and Zn and total ferrochrome dust are emitted into theatmosphere were determined. The extent of soil contamination bythe dust deposited around the smelter in the generally prevailingsoutheasterly wind direction around the smelter was carried out.The highest concentrations of Cr and Fe occurred in the fineparticulates of sizes less than 59 m whilst that of Cu and Znoccurred in the coarse particulates of size range 70-100 m.The emission rates from stack 2 were; total ferrochromeparticulates 62.17 kg h^-1, Cr 6.217 kg h^-1, Fe 2.423 kg h^-1, Zn42 mg h^-1 and 6 mg h^-1 for Cu. Particulate matter was emitted at arate of 289 mg m^-3 from stack number 2. This value exceeds thelegal limit of 200 mg m^-3. Chromium and iron are the metalsin the largest amounts. The particles that constitute the largestproportion of the dust were in the range of 58-107.5 m. Thisis a characteristic feature of the particulate matter emissionsfrom ZIMASCO. Soils in the downwind direction from the smelterwere polluted with Cr up to a distance of about 700 m outward fromthe perimeter of the boundary of the smelter.     

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.