Evolution of anthropogenic aerosols in the coastal town of Salina Cruz, Mexico: part I particle dynamics and land-sea interactions

Measurements of aerosol particles in a coastal city in southeast Mexico show that the concentrations and optical properties are strongly linked to land and sea breezes. Maximum concentrations of condensation nuclei (CN), black carbon (BC) and particle bound polycyclic aromatic hydrocarbons (PPAH) occur during land breeze periods and decrease with the sea breeze. The concentrations of particles in air from the ocean, however, remain significantly above background, maritime values as a result of the recirculation of anthropogenic emissions. The mass size distribution is dominated by particles larger than 5 microm when wind speeds exceed 4 m s(-1); otherwise, the uptake of water vapor onto unactivated particles is the process that dominates the growth of particles. Precipitation removes particles larger than 5 microm but CN, BC and PPAH concentrations are minimally affected.     

Concentration and chemical characteristics of PM2.5 in Beijing, China: 2001-2002

Weekly PM2.5 samples were simultaneously collected at a semi-residential (Tsinghua University) and a downtown (Chegongzhuang) site in Beijing from August 2001 through September 2002. The ambient mass concentration and chemical composition of PM2.5 were determined. Analyses including elemental composition, water-soluble ions, and organic and elemental carbon were performed. The annual average concentrations of PM2.5 were 96.5 microg m(-3) and 106.9 microg m(-3) at CGZ and HU site, respectively. More than 80% of the PM2.5 mass concentrations were explained by carbonaceous species, secondary particles, crustal matters and trace elements at the two sites. Carbonaceous species were the most abundant components, constituting about 45% and 48% of the total PM2.5 mass concentrations at CGZ and THU site, respectively. SO4(2-), NO3- and NH4+ were three major ions, accounting for 37%, 23% and 20%, respectively, of the total mass of inorganic water-soluble ions.     

Characterizing air pollution in two low-income neighborhoods in Accra, Ghana

Sub-Saharan Africa has the highest rate of urban population growth in the world, with a large number of urban residents living in low-income "slum" neighborhoods. We conducted a study for an initial assessment of the levels and spatial and/or temporal patterns of multiple pollutants in the ambient air in two low-income neighborhoods in Accra, Ghana. Over a 3-week period we measured (i) 24-hour integrated PM(10) and PM(2.5) mass at four roof-top fixed sites, also used for particle speciation; (ii) continuous PM(10) and PM(2.5) at one fixed site; and (iii) 96-hour integrated concentration of sulfur dioxide (SO(2)) and nitrogen dioxide (NO(2)) at 30 fixed sites. We also conducted seven consecutive days of mobile monitoring of PM(10) and PM(2.5) mass and submicron particle count. PM(10) ranged from 57.9 to 93.6 microg/m(3) at the four sites, with a weighted average of 71.8 microg/m(3) and PM(2.5) from 22.3 to 40.2 microg/m(3), with an average of 27.4 microg/m(3). PM(2.5)/PM(10) ratio at the four fixed sites ranged from 0.33 to 0.43. Elemental carbon (EC) was 10-11% of PM(2.5) mass at all four measurement sites; organic matter (OM) formed slightly less than 50% of PM(2.5) mass. Cl, K, and S had the largest elemental contributions to PM(2.5) mass, and Cl, Si, Ca, Fe, and Al to coarse particles. SO(2) and NO(2) concentrations were almost universally lower than the US-EPA National Ambient Air Quality Standards (NAAQS), with virtually no variation across sites. There is evidence for the contributions from biomass and traffic sources, and from geological and marine non-combustion sources to particle pollution. The implications of the results for future urban air pollution monitoring and measurement in developing countries are discussed.     

Indoor air quality in the university libraries of Modena (Italy)

We carried out a survey in 16 libraries of the University of Modena, Northern Italy, to assess the indoor exposure to volatile organic compounds (VOCs), including formaldehyde, and total dusts. Data were collected on the main structural characteristics of the buildings; indoor microclimate parameters, such as temperature, relative humidity and ventilation rate were measured and air samples taken inside and outside the libraries. The mean value of total dusts was 190 +/- 130 microg/m3 with a wide range of values. Formaldehyde was found in only ten out of 16 libraries and the indoor concentrations ranged from 1.70 to 67.8 microg/m3 with an average value of 32.7 +/- 23.9 microg/m3. On the whole, VOCs were present in all the libraries investigated with an average value was 433 +/- 267 microg/m3 (range 102-936 microg/m3). No correlation was found among VOCs, formaldehyde and total dusts nor was a significant association observed with microclimatic parameters or the structural characteristics of the buildings. The general situation found in this study suggests no major problems related to indoor pollution. However, some of the pollutants investigated such as total dust and total VOCs deserve further investigation. It is important to identify the possible sources of contaminants and to define the relationship between indoor and outdoor levels of pollutants more accurately, taking into account the effects of air recycling due to natural ventilation systems.     

Measuring the exposure of infants and children to indoor air pollution from biomass fuels in The Gambia

Indoor air pollution (IAP) from biomass fuels contains high concentrations of health damaging pollutants and is associated with an increased risk of childhood pneumonia. We aimed to design an exposure measurement component for a matched case-control study of IAP as a risk factor for pneumonia and severe pneumonia in infants and children in The Gambia. We conducted co-located simultaneous area measurement of carbon monoxide (CO) and particles with aerodynamic diameter <2.5 microm (PM(2.5)) in 13 households for 48 h each. CO was measured using a passive integrated monitor and PM(2.5) using a continuous monitor. In three of the 13 households, we also measured continuous PM(2.5) concentration for 2 weeks in the cooking, sleeping, and playing areas. We used gravimetric PM(2.5) samples as the reference to correct the continuous PM(2.5) for instrument measurement error. Forty-eight hour CO and PM(2.5) concentrations in the cooking area had a correlation coefficient of 0.80. Average 48-h CO and PM(2.5) concentrations in the cooking area were 3.8 +/- 3.9 ppm and 361 +/- 312 microg/m3, respectively. The average 48-h CO exposure was 1.5 +/- 1.6 ppm for children and 2.4 +/- 1.9 ppm for mothers. PM(2.5) exposure was an estimated 219 microg/m3 for children and 275 microg/m3 for their mothers. The continuous PM(2.5) concentration had peaks in all households representing the morning, midday, and evening cooking periods, with the largest peak corresponding to midday. The results are used to provide specific recommendations for measuring the exposure of infants and children in an epidemiological study. PRACTICAL IMPLICATIONS: Measuring personal particulate matter (PM) exposure of young children in epidemiological studies is hindered by the absence of small personal monitors. Simultaneous measurement of PM and carbon monoxide suggests that a combination of methods may be needed for measuring children's PM exposure in areas where household biomass combustion is the primary source of indoor air pollution. Children's PM exposure in biomass burning homes in The Gambia is substantially higher than concentrations in the world's most polluted cities.     

Characteristics of PM10, SO2, NO(x) and O3 in ambient air during the dust storm period in Beijing

In this study, the hourly variations of the mass concentrations of PM10, SO2, NO(x) and O3 at three sampling sites were observed in Beijing during dust storm occurrence period in April 2000. The PM2.5 samples were simultaneously collected. By comparing the hourly variations of the pollutant concentrations before, during and after dust storm event and haze pollution episode, the variation characteristics of the mass concentrations of PM10, SO2, NO(x) and O3 during dust storm events were presented. The results show that the mass concentration of PM10 reached 1500 microg m(-3) during dust storm events on April 6 and 25, 2000, which was 5-10 times that of the non-dust weather conditions, and this period of high mass concentration of PM10 lasted for about 14 h, and then the concentration level prior to the dust event was recovered in 6-h time period. Due to the strong wind, the concentrations of SO2, NO(x), NO2 and O3 during dust storm period were maintained at low levels, which was significantly different from those on non-dust storm and haze pollution conditions. A lot of coarse particles as well as a very large amount of fine particles were contained in the atmospheric particulates during dust storm period, and the concentration level of PM2.5 was comparable to that during haze pollution episode. During the dust storm period, the PM2.5 concentration was approximately 230 microg m(-3), accounting for 30% of the total PM10 mass concentration, was four times that of non-dust weather conditions, and the crustal elements constituted about 66.4% of the chemical composition of PM2.5 while sulfate and nitrate contributed much less, which was quite different from the chemical composition of PM2.5 primarily constituted by sulfate, nitrate and organics on haze pollution day.     

Elevated concentrations of 1-hydroxypyrene in schoolchildren during winter in Christchurch, New Zealand

Particulate air pollution is significantly elevated during the winter in Christchurch, New Zealand, largely attributable to use of wood burners for domestic home heating, topography, and meteorological conditions. Polycyclic aromatic hydrocarbons (PAHs) are a key component of airborne particulate matter (PM) and urinary 1-hydroxypyrene (1-OHP) has previously been used to assess exposure of people to PAHs. We examined urinary 1-OHP in Christchurch male non-smoking schoolchildren (12-18 yr) on two occasions after high pollution events (48 and 72 microg PM(10)/m(3) 24-h average) and two occasions during periods of low pollution (19 and 12 microg PM(10)/m(3)). Concentrations of urinary 1-OHP were significantly elevated in the students during high pollution events (median (mean+/-SD) 0.043 (0.051+/-0.032) and 0.042 (0.060+/-0.092) micromol OHP/mol creatinine respectively) compared with low pollution periods (median (mean+/-SD) 0.019 (0.026+/-0.032) and 0.025 (0.028+/-0.018) micromol/mol creatinine respectively). The observed 1-OHP concentrations are at the lower end of those determined in children and non-occupationally exposed adults in international studies and suggest a generally low exposure to PAHs. The increased urinary 1-OHP concentrations following nights of elevated particulate concentrations in ambient air suggest increased exposure to ambient air pollution during winter time, and could potentially be used as a biomarker of exposure in this population.     

Single particle and inorganic characterization of rainwater collected above the North Sea

Suspended matter and the dissolved fraction of rainwater collected above the North Sea were characterized using electron probe X-ray microanalysis (EPXMA), inductively coupled plasma-optical emission spectrometry (ICP-OES) and ion chromatography (IC), respectively. Suspended particulate matter was dominated by aluminosilicates and organic particles. Fifteen particle types describe the composition of the North Sea rainwater suspended matter. Factor analysis, particle size distributions and manual EPXMA measurements illustrated the complex genesis of different particle types: terrigenous; biogenic (both marine and continental); and anthropogenic. It was demonstrated that at the beginning of a shower of rain the coarse particles that are present in the air under the cloud are washed out, while during the second phase rainout particles, formed in the cloud, become more important due to the absence of new coarse particles under the cloud. Above the sea, the total amount of suspended matter (TSM) is much smaller and more variable than above the land and also the decrease in particle diameter is less visible. Approximately 10% of the studied particles contained trace heavy metals. The dissolved compounds in the North Sea rainwater were also variable in time and space. In general, over a short period of time, the concentrations of all dissolved compounds seem to decrease during a shower, but this decrease is much larger above land than above sea. The concentrations of dissolved trace metals present in rainwater above the southern North Sea has decreased over the last 15 years.     

Occupational exposure to trihalomethanes in indoor swimming pools

The study evaluated occupational exposure to trihalomethanes (THMs) in indoor swimming pools. Thirty-two subjects, representing the whole workforce employed in the five public indoor swimming pools in the city of Modena (Northern Italy) were enrolled. Both environmental and biological monitoring of THMs exposure were performed. Environmental concentrations of THMs in different areas inside the swimming pools (at the poolside, in the reception area and in the engine-room) were measured as external exposure index, while individual exposure of swimming pool employees was estimated by THMs concentration in alveolar air. The levels of THMs observed in swimming pool water ranged from 17.8 to 70.8 microg/l; the mean levels of THMs in ambient air were 25.6+/-24.5 microg/m3 in the engine room, 26.1+/-24.3 microg/m3 in the reception area and 58.0+/-22.1 microg/m3 at the poolside. Among THMs, only chloroform and bromodichloromethane were always measured in ambient air, while dibromochloromethane was detected in ambient air rarely and bromoform only once. Biological monitoring results showed a THMs mean value of 20.9+/-15.6 microg/m3. Statistically significant differences were observed according to the main job activity: in pool attendants, THMs alveolar air were approximately double those observed in employees working in other areas of the swimming pools (25.1+/-16.5 microg/m3 vs. 14.8+/-12.3 microg/m3, P < 0.01). THMs in alveolar air samples were significantly correlated with THMs concentrations in ambient air (r = 0.57; P < 0.001). Indoor swimming pool employees are exposed to THMs at ambient air levels higher than the general population. The different environmental exposure inside the swimming pool can induce a different internal dose in exposed workers. The correlation found between ambient and alveolar air samples confirms that breath analysis is a good biological index of occupational exposure to these substances at low environmental levels.     

Foliar exchange of mercury as a function of soil and air mercury concentrations

Previous research has indicated that foliar mercury (Hg) flux is bi-directional, with influence from both atmospheric and soil Hg. This work investigated the role of soil and air Hg concentrations on foliar Hg exchange using a single-plant gas-exchange system. The exchange of Hg vapor with aspen seedlings grown in soil Hg concentrations of 0.03+/-0.01, 5.8+/-0.5, and 12.3+/-1.3 microg g(-1) and exposed to atmospheric Hg concentrations of 2.4+/-0.5, 11.0+/-0.9, and 30.4+/-2.2 ng m(-3) was measured. At background atmospheric Hg concentrations of 2.4 ng m(-3), foliage released Hg at all three soil Hg concentrations and fluxes ranged from 1.6 to 5.5 ng/m(2)/h. At higher atmospheric Hg concentrations (>11 ng m(-3)), net deposition to foliage ranged from -9 to -47 ng/m(2)/h, exhibiting increase uptake with higher air Hg concentrations. Fluxes associated with aspen showed an immediate response to changes in atmospheric Hg concentrations. Compensation points, the air concentration where no net flux of Hg vapor occurred, were 3-4 ng m(-3) in the light and 2-3 ng m(-3) in the dark for trees grown in soils of 0.03 and 6 microg g(-1) Hg content, and 5-6 ng m(-3) in the light and 2.5-3.5 ng m(-3) in the dark for trees grown in 12 microg g(-1) Hg soils.     

Particulate matter and carbon monoxide multiple regression models using environmental characteristics in a high diesel-use area of Baguio City, Philippines

In Baguio City, Philippines, a mountainous city of 252,386 people where 61% of motor vehicles use diesel fuel, ambient particulate matter <2.5 microm (PM(2.5)) and <10 microm (PM(10)) in aerodynamic diameter and carbon monoxide (CO) were measured at 30 street-level locations for 15 min apiece during the early morning (4:50-6:30 am), morning rush hour (6:30-9:10 am) and afternoon rush hour (3:40-5:40 pm) in December 2004. Environmental observations (e.g. traffic-related variables, building/roadway designs, wind speed and direction, etc.) at each location were noted during each monitoring event. Multiple regression models were formulated to determine which pollution sources and environmental factors significantly affect ground-level PM(2.5), PM(10) and CO concentrations. The models showed statistically significant relationships between traffic and early morning particulate air pollution [(PM(2.5)p=0.021) and PM(10) (p=0.048)], traffic and morning rush hour CO (p=0.048), traffic and afternoon rush hour CO (p=0.034) and wind and early morning CO (p=0.044). The mean early morning, street-level PM(2.5) (110+/-8 microg/m3; mean+/-1 standard error) was not significantly different (p-value>0.05) from either rush hour PM(2.5) concentration (morning=98+/-7 microg/m3; afternoon=107+/-5 microg/m3) due to nocturnal inversions in spite of a 100% increase in automotive density during rush hours. Early morning street-level CO (3.0+/-1.7 ppm) differed from morning rush hour (4.1+/-2.3 ppm) (p=0.039) and afternoon rush hour (4.5+/-2.2 ppm) (p=0.007). Additionally, PM(2.5), PM(10), CO, nitrogen dioxide (NO2) and select volatile organic compounds were continuously measured at a downtown, third-story monitoring station along a busy roadway for 11 days. Twenty-four-hour average ambient concentrations were: PM(2.5)=72.9+/-21 microg/m3; CO=2.61+/-0.6 ppm; NO2=27.7+/-1.6 ppb; benzene=8.4+/-1.4 microg/m3; ethylbenzene=4.6+/-2.0 microg/m3; p-xylene=4.4+/-1.9 microg/m3; m-xylene=10.2+/-4.4 microg/m3; o-xylene=7.5+/-3.2 microg/m3. The multiple regression models suggest that traffic and wind in Baguio City, Philippines significantly affect street-level pollution concentrations. Ambient PM(2.5) levels measured are above USEPA daily (65 microg/m3) and Filipino/USEPA annual standards (15 microg/m3) with concentrations of a magnitude rarely seen in most countries except in areas where local topography plays a significant role in air pollution entrapment. The elevated pollution concentrations present and the diesel-rich nature of motor vehicle emissions are important pertaining to human exposure and health information and as such warrant public health concern.     

Manganese concentrations in the soil and air in the vicinity of a closed manganese alloy production plant

In Montreal (Canada), the mean annual atmospheric Mn concentrations between 1981 and 1990 were stable, followed by a decrease of almost 50% from 1990 to 1992. The reason for such a decrease in Mn is probably the shutdown of a large manganese alloy production plant in Beauharnois, approximately 25 km from Montreal. The objective of this study is to assess the level of air and soil contamination by Mn in the vicinity of this ferroalloy plant more than 10 years after its closure. Air and soil were sampled over 5 days at two and three sites, respectively. Site 1 was located 10 m NE of the closed plant, in the direction of the prevailing SW-NE winds. Sites 2 and 3 were at 50 and 800 m SE from the plant. Air samples were collected in order to determine total (MnT) and respirable (MnR). Soil samples were taken in the surface and subsurface strata. The results show that site 1 is extremely polluted with a mean Mn concentration in surface strata of 2,66,000+/-45,000 ppm and 2,83,000+/-23,000 ppm in the subsurface strata, while the average MnT and MnR are 21.9+/-13.7 and 3.5+/-3.9 microg/m(3), respectively. The explanation for this contamination is direct deposition on the soil of solid Mn-rich residue and atmospheric erosion of Mn particles. The situation should be remediated by the public authority with high priority.     

A Pb isotope and trace element study of rainwater from the Massif Central (France)

Lead isotope ratios and Zn, Pb, Cu, Cd, Sb and Rb contents were measured in samples of rainwater collected over a period of 15 months from the Massif Central (France). Each sample, collected automatically at monthly intervals, represents a series of rainfall events. Rainwater chemistry was interpreted in terms of the chemical contributions from wet deposition and from different source regions for dust in the centre of France. Trace element concentrations in rainwater samples showed a wide range, particularly for Pb (1.30-465 microg/l), with variations decreasing for Cd (0.07-1.70 microg/l), Zn (1.00-54.00 microg/l), Cu (0.20-25.00 microg/l), Sb (approximately 0-0.33 microg/l) and Ni (approximately 0-15.00 microg/l). Trace element contents do not correlate with rainfall amount and no inter-element correlations are evident in the data. Lead is the most common trace metal found in the rainwater (mean value = 996 microg/m2/y) while Sb is the least common element measured (mean value = 1.12 microg/m2/y). The composition of rainwater collected from the Massif Central shows a range in Pb isotope ratios from 17.935 to 19.22 (206Pb/204Pb), 15.578 to 15.73 (207Pb/204Pb) and 37.559 to 38.606 (208Pb/204Pb). A five-component mixing model involving contributions from the natural background, gasoline inputs from industrial and agricultural activity and a source resulting from mining waste may be used to explain both the Pb isotope signature and the fluctuations in trace metal contents of Massif Central rainwater.     

Strontium isotope and major ion chemistry of the rainwaters from Guiyang, Guizhou Province, China

Twenty-two rainwater samples from Guiyang city, southwestern China, have been analyzed for their chemical compositions and 87Sr/86Sr ratios, with a main purpose to get a better understanding of the general features of rainwater in Guiyang city and their correspondences to human activities. The rainwaters studied are almost acidic (pH=4.53) and show big changes in major ion composition. Ca2+ and Mg2+ are the principal cations in the rainwaters and their mean values are 56.6 micromol/L (12.5-163.8 micromol/L) and 12.8 micromol/L (4.5-47.3 micromol/L ), respectively. The sum of Ca2+ and Mg2+ accounts for 78%-96% of the total cations in the studied rainwaters. Na+ was the least abundant of the major cations with a mean content of 4 micromol/L (0.9-7.8 micromol/L). SO4(2-) is the predominant anion, with a mean content of 94 micromol/L (33.5-279.4 micromol/L), coming next is NO(3-) with a mean content of 48 micromol/L (2.1-251.8 micromol/L). SO4(2-) and NO(3-) together account for 77%-99% of the total anions. Ca2+ and Mg2+ in the rainwater are most likely from dissolution of carbonate minerals in dust or aerosol, unlike K+ that shows more contribution of anthropogenic sources to the rainwater. Na+ does not vary in concentration with Cl-. Significant enrichment of Cl- relative to Na+ as compared with sea water indicates negligible contribution of marine source, which is supported by the evidence that the total rainwater samples show lower 87Sr/86Sr ratios (ranging from 0.707934 to 0.709080) than sea water. The rainwater samples are characterized by high contents of NO(3-), SO4(2-), and Cl- relative to Na+, as compared to the rainwater from other areas in the world, suggesting that the anions (NO(3-), SO4(2-), and Cl-) have mainly of anthropogenic sources. Sr isotope shows potential to trace sources of contaminants when combined with other chemical factors: covariation of 87Sr/86Sr ratio with Cl-/Na+ in the rainwater suggest presence of at least two anthropogenic sources for the rainwater samples studied. The coal-combustion industries are probably the major atmospheric contaminant sources in Guiyang city.     

PM2.5 chemical composition in Hong Kong: urban and regional variations

Chemically speciated PM2.5 measurements were made at roadside, urban, and rural background sites in Hong Kong for 1 year during 2000/2001 to determine the spatial and temporal variations of PM2.5 mass and chemical composition in this highly populated region. Annual average PM2.5 concentrations at the urban and rural sites were 34.1 and 23.7 microg m(-3), respectively, approximately 50-100% higher than the United States' annual average National Ambient Air Quality Standard (NAAQS) of 15 microg m(-3). Daily PM2.5 concentrations exceeded the U.S. 24-h NAAQS of 65 microg m(-3) on 19 days, reaching 131+/-8 microg m(-3) at the roadside site on 02/28/2001. Carbonaceous aerosol is the largest contributor to PM2.5 mass (explaining 52-75% of PM2.5 mass at the two urban sites and 32% at the background site), followed by ammonium sulfate (ranging from 23% to 37% at the two urban sites and 51% at the background site). Ammonium sulfate and crustal concentrations showed more uniform spatial distributions, while the largest urban-rural contrasts found in carbonaceous aerosol (likely due to emissions from on-road gasoline and diesel vehicles). Marine influences accounted for 7% of the mass at the background site (more than twice as much as at the two urban sites). Ternary diagrams are utilized to illustrate the different spatial patterns.     

Temporal variations of PM2.5 in the ambient air of a suburban site in Athens, Greece

Twenty-three hour measurements of PM(2.5) particulate matter have been carried out during the period between the 1st April and the 13th November 2003 in a suburban area of Athens. The monitoring site was located in the National Research Center "DEMOKRITOS", on the foot of Hemittos Mountain and about 12 km away from the center of Athens. The site covers an area of 600 acres in a forest of pine trees close enough to the newly constructed Hemittos Mountain peripheral highway. PM(2.5) samples were collected on 47 mm filters, with the use of low volume gravimetric samplers while a meteorological station recorded meteorological data 6 m above the ground, nearby the sampling instrumentation. The daily average PM(2.5) concentration reached 21.1 microg m(-3) and all measurements were below U.S. Environmental Pollution Agency daily limit (65 microg m(-3)). A regression analysis was used to investigate the relationship among PM(2.5) concentrations and meteorological parameters. Additionally, PM(2.5) mass concentrations were correlated with other inorganic gaseous pollutants (O(3), NO, NO(2), SO(2)) while weekly and seasonal PM(2.5) variations were also investigated.     

An assessment of indoor air contaminants in buildings with recreational activity

Indoor air quality measurements were carried out during three concerts and one ice hockey game in three different halls. Gas phase components consisted of CO2, CO, and NO whereas for particulate indicators, measurements of particle mass distributions (0.05-9 microm), particle number distributions (0.75-10 microm), and particle bound polycyclic aromatic hydrocarbons (pPAH) were carried out. The calculated ventilation rates did not meet the ventilation requirements for rooms with occupants who smoke to be perceived as acceptable by 80% of the occupants. Average PM9 (mass of particulate matter with an aerodynamic diameter < 9 microm) concentrations throughout the events ranged from 318 to 2000 microg m(-3). Particle concentrations in the size range < 0.4 microm measured 203-696 microg m(-3), the majority of it being attributed to environmental tobacco smoke (ETS). For particle numbers > 0.75 microm concentrations ranged from 2 x 10(4) to 1.9 x 10(5) particles per l while for pPAH, concentrations from 336 to 990 ng m(-3) were observed. The average event concentrations for the gaseous component CO2 ranged from 1110 to 1700 ppm, for CO 2-3.1 ppm and for NOx 237 ppb. The event to baseline concentration ratios for gaseous components ranged from 1.1 to 4.3 while for particulate indicators generally much greater ratios between 0.7 and 140 were found. Possible health effects inflicted by an exposure based on the measured concentrations of the various parameters are discussed.     

Elemental carbon and respirable particulate matter in the indoor air of apartments and nursery schools and ambient air in Berlin (Germany)

This study was performed to examine exposure to typical carcinogenic traffic air pollutants in the city center of an urban area. In all, 123 apartments and 74 nursery schools were analyzed with and without tobacco smoke interference and the households in two measuring periods. Simultaneously, the air outside 61 apartment windows as well as the average daily traffic volume were measured. Elemental carbon (EC), the marker for particulate diesel exhaust and respirable particulate matter (RPM) were determined. The thermographic EC analysis was conducted with and without prior solvent extraction of the soluble carbon fraction. Comparison of these two thermographic EC measurements clearly showed that method-related differences in the results, especially for indoor measurements, when high background loads of organic material were present (e.g. tobacco smoke), existed. Solvent extraction prior to EC determination was therefore appropriate. For the first winter measuring period, the EC concentration levels without solvent extraction in the indoor air were about 50% higher than those measured in the spring/summer period. In the second measuring period (i.e. spring/summer), the median EC concentrations after solvent extraction were 1.9 microg/m3 for smokers' apartments and 2.1 microg/m3 for non-smokers' apartments, with RPM concentrations of 57 and 27 microg/m3, respectively. Nursery schools showed high concentrations with median values of 53 microg/m3 for RPM and 2.9 microg/m3 for EC after solvent extraction. A significant correlation between the fine dust and EC concentrations (after solvent extraction) in the indoor and ambient air was determined. Outdoor EC values were also correlated with the average daily traffic volume. The EC ratios between indoor and ambient concentration showed a median of 0.8 (range: 0.3-4.2) in non-smoker households and 0.9 (range: 0.4-1.5) in smoker apartments. Furthermore, the EC/RPM ratio in indoor and ambient air was 0.01-0.15 (median 0.06) and 0.04-0.37 (median 0.09), respectively. PRACTICAL IMPLICATIONS: In the absence of indoor sources a significant correlation with regard to respirable particulate matter (RPM) and elemental carbon concentrations between the indoor and ambient air of apartments was observed. The high degree of certainty resulting from this correlation underscores the importance of ambient air concentrations for indoor air quality. In nursery schools we found higher concentrations of RPM. An explanation of these results could be the high number of occupants in the room, their activity and the cleaning intensity.     

Particulate matter exposure along designated bicycle routes in Vancouver, British Columbia

An instrumented bicycle was used to elucidate particulate matter exposures along bicycle routes passing through a variety of land uses over 14 days during summer and fall in a mid-latitude traffic dominated urban setting. Overall, exposures were low or comparable to those found in studies elsewhere (mean PM(2.5) and PM(10) concentrations over each daily bicycle traverse varied between 7-34 microg m(-3) and 26-77 microg m(-3) respectively). Meteorological factors were responsible for significant day-to-day variability with PM(2.5) positively correlated with air temperature, PM(10) negatively correlated with precipitation, and ultrafine particles negatively correlated with both air temperature and wind speed. On individual days, land use and proximity to traffic were factors significantly affecting exposure along designated bicycle routes. While concentrations of PM(2.5) were found to be relatively spatially uniform over the length of the study route, PM(10) showed a more heterogeneous spatial distribution. Specifically, construction sites and areas susceptible to the suspension of road dust have higher concentrations of coarse particles. Ultrafine particles were also heterogeneously distributed in space, with areas with heavy traffic volumes having the highest concentrations. Observations show qualitative agreement in terms of spatial patterns with a land-use regression (LUR) model for annual PM(2.5) concentrations.     

Indoor/outdoor relationships for PM2.5 and associated carbonaceous pollutants at residential homes in Hong Kong - case study

Six residences were selected (two roadside, two urban, and two rural) to evaluate the indoor-outdoor characteristics of PM(2.5) (aerodynamic diameter <2.5 microm) carbonaceous species in Hong Kong during March and April 2004. Twenty-minute-averaged indoor and outdoor PM(2.5) concentrations were recorded by DustTrak samplers simultaneously at each site for 3 days to examine diurnal variability of PM(2.5) mass concentrations and their indoor-to-outdoor (I/O) ratios. Daily (24-h average) indoor/outdoor PM(2.5) samples were collected on pre-fired quartz-fiber filters with battery-powered portable mini-volume samplers and analyzed for organic and elemental carbon (OC, EC) by thermal/optical reflectance (TOR) following the Interagency Monitoring of Protected Visual Environments (IMPROVE) protocol. The average indoor and outdoor concentrations of 24 h PM(2.5) were 56.7 and 43.8 microg/m(3), respectively. The short-term PM(2.5) profiles indicated that the penetration of outdoor particles was an important contributor to indoor PM(2.5), and a household survey indicated that daily activities were also sources of episodic peaks in indoor PM(2.5). The average indoor OC and EC concentrations of 17.1 and 2.8 microg/m(3), respectively, accounted for an average of 29.5 and 5.2%, respectively, of indoor PM(2.5) mass. The average indoor OC/EC ratios were 5.8, 9.1, and 5.0 in roadside, urban, and rural areas, respectively; while average outdoor OC/EC ratios were 4.0, 4.3, and 4.0, respectively. The average I/O ratios of 24 h PM(2.5), OC, and EC were 1.4, 1.8, and 1.2, respectively. High indoor-outdoor correlations (r(2)) were found for PM(2.5) EC (0.96) and mass (0.81), and low correlations were found for OC (0.55), indicative of different organic carbon sources indoors. A simple model implied that about two-thirds of carbonaceous particles in indoor air are originated from outdoor sources. PRACTICAL IMPLICATIONS: Indoor particulate pollution has received more attentions in Asia. This study presents a case study regarding the fine particulate matter and its carbonaceous compositions at six residential homes in Hong Kong. The characteristics and relationship of atmospheric organic and elemental carbon were discussed indoors and outdoors. The distribution of eight carbon fractions was first reported in indoor samples to interpret potential sources of indoor carbonaceous particles. The data set can provide significant scientific basis for indoor air quality and epidemiology study in Hong Kong and China.