Abstract  OBJECTIVES: To estimate long-term exposure to traffic-related air pollutants on an individual basis and to assess adverse health effects using a combination of air pollution measurement data, data from geographical information systems (GIS) and questionnaire data. METHODS: 40 measurement sites in the city of Munich, Germany were selected at which to collect particulate matter with a 50% cut-off aerodynamic diameter of 2.5 microm (PM2.5) and to measure PM2.5 absorbance and nitrogen dioxide (NO2). A pool of GIS variables (information about street length, household and population density and land use) was collected for the Munich metropolitan area and was used in multiple linear regression models to predict traffic-related air pollutants. These models were also applied to the birth addresses of two birth cohorts (German Infant Nutritional Intervention Study (GINI) and Influence of Life-style factors on the development of the Immune System and Allergies in East and West Germany (LISA)) in the Munich metropolitan area. Associations between air pollution concentrations at birth address and 1-year and 2-year incidences of respiratory symptoms were analysed. RESULTS: The following means for the estimated exposures to PM2.5, PM2.5 absorbance and NO2 were obtained: 12.8 microg/m3, 1.7x10(-5) m(-1) and 35.3 mug/m3, respectively. Adjusted odds ratios (ORs) for wheezing, cough without infection, dry cough at night, bronchial asthma, bronchitis and respiratory infections indicated positive associations with traffic-related air pollutants. After controlling for individual confounders, significant associations were found between the pollutant PM2.5 and sneezing, runny/stuffed nose during the first year of life (OR 1.16, 95% confidence interval 1.01 to 1.34) Similar effects were observed for the second year of life. These findings are similar to those from our previous analysis that were restricted to a subcohort in Munich city. The extended study also showed significant effects for sneezing, running/stuffed nose. Additionally, significant associations were found between NO2 and dry cough at night (or bronchitis) during the first year of life. The variable "living close to major roads" (<50 m), which was not analysed for the previous inner city cohort with birth addresses in the city of Munich, turned out to increase the risk of wheezing and asthmatic/spastic/obstructive bronchitis. CONCLUSIONS: Effects on asthma and hay fever are subject to confirmation at older ages, when these outcomes can be more validly assessed.

Abstract  BACKGROUND: Otitis media is one of the most common infections in young children. Although exposure to environmental tobacco smoke is a known risk factor associated with otitis media, little information is available regarding the potential association with air pollution. OBJECTIVE: We set out to study the relationship between exposure to traffic-related air pollution and otitis media in two birth cohorts. METHODS: Individual estimates of outdoor concentrations of traffic-related air pollutants-nitrogen dioxide, fine particles [particulate matter with aerodynamic diameters

Abstract  Aims: To investigate the chronic effects of air pollution caused mainly by automobiles in healthy adult females. Methods: Respiratory symptoms were investigated in 5682 adult females who had lived in the Tokyo metropolitan area for three years or more in 1987; 733 of them were subjected to pulmonary function tests over eight years from 1987 to 1994. The subjects were divided into three groups by the level of air pollution they were exposed to during the study period. The concentrations of nitrogen dioxide and suspended particulate matter were the highest in group 1, and the lowest in group 3. Results: The prevalence rates of respiratory symptoms in group 1 were higher than those in groups 2 and 3, except for wheezing. Multiple logistic regression analysis showed significant differences in persistent phlegm and breathlessness. The subjects selected for the analysis of pulmonary function were 94, 210, and 102 females in groups 1, 2, and 3, respectively. The annual mean change of FEV1 in group 1 was the largest (-0.020 l/y), followed by that in group 2 (-0.015 l/y), and that in group 3 (-0.009 l/y). Testing for trends showed a significant larger decrease of FEV1 with the increase in the level of air pollution. Conclusions: The subjects living in areas with high levels of air pollution showed higher prevalence rates of respiratory symptoms and a larger decrease of FEV1 compared with those living in areas with low levels of air pollution. Since the traffic density is larger in areas with high air pollution, the differences among the groups may reflect the effect of air pollution attributable to particulate matter found in automobile exhaust.

Abstract  For a period of almost 3 years, sampling of size-fractionated ambient particulate matter with diameter below 10 Ám (PM10) was performed at urban source sites (Downey and University of Southern California) and inland receptor sites (Claremont and Riverside) in the Los Angeles Basin as part of the Southern California Particle Center and Supersite. Results for size-resolved PM10 mass, inorganic ions (sulfate and nitrate), metals, elemental carbon, and organic carbon were obtained. Three collocated micro-orifice uniform deposit impactors (MOUDIs) were deployed to collect 24-hour samples roughly once a week. Ultrafine particle concentrations (particle diameter d p < 0.1 Ám) were found to be the highest at the source sites resulting from fresh vehicular emissions. Mass concentrations in the accumulation mode (0.1 < d p < 2.5 Ám) were lower in winter than in summer, especially at the receptor sites. PM concentrations in the coarse mode (2.5 < d p < 10 Ám) were lower in winter and were composed mostly of nitrate and crustal elements (iron, calcium, potassium, silicon, and aluminum). Consistent relative levels of these elements indicate a common source of soil and/or road dust. In the accumulation mode, nitrate and organic carbon were predominant with higher nitrate levels found at the receptor sites. The ultrafine mode PM consisted of mostly organic carbon, with higher wintertime levels at the source sites due to increased organic vapor condensation from vehicles at lower temperatures. Conversely, higher ultrafine organic carbon levels at the receptor areas are due to secondary organic aerosol formation by photochemical reactions as well as increased advection of polluted air masses from upwind.

Abstract  Measurements of NO and NO2 are reported using a highly modified photofragmentation two-photon laser-induced fluorescence (PF-TP-LIF) instrument. Available evidence suggests that the changes made substantially reduced wall decomposition of labile NOy species. In sharp contrast to the results reported from NASA's 1991 PEM-West A program where the median value for the ratio (NO2)(meas)/(NO2)(calc) was 3.36, the PEM-Tropics A observations produced a value for this ratio of 0.93. This represents the first time that remote upper tropospheric NO-NO2 data have shown a high degree of correspondence with current photochemical mechanisms.

Abstract  Background: Studies in monkeys with intranasally instilled gold ultrafine particles (UFPs; < 100 nm) and in rats with inhaled carbon UFPs suggested that solid UFPs deposited in the nose travel along the olfactory nerve to the olfactory bulb. Methods: To determine if olfactory translocation occurs for other solid metal UFPs and assess potential health effects, we exposed groups of rats to manganese (Mn) oxide UFPs (30 nm; ~ 500 μg/m3) with either both nostrils patent or the right nostril occluded. We analyzed Mn in lung, liver, olfactory bulb, and other brain regions, and we performed gene and protein analyses. Results: After 12 days of exposure with both nostrils patent, Mn concentrations in the olfactory bulb increased 3.5-fold, whereas lung Mn concentrations doubled; there were also increases in striatum, frontal cortex, and cerebellum. Lung lavage analysis showed no indications of lung inflammation, whereas increases in olfactory bulb tumor necrosis factor-α mRNA (~ 8-fold) and protein (~ 30-fold) were found after 11 days of exposure and, to a lesser degree, in other brain regions with increased Mn levels. Macrophage inflammatory protein-2, glial fibrillary acidic protein, and neuronal cell adhesion molecule mRNA were also increased in olfactory bulb. With the right nostril occluded for a 2-day exposure, Mn accumulated only in the left olfactory bulb. Solubilization of the Mn oxide UFPs was < 1.5% per day. Conclusions: We conclude that the olfactory neuronal pathway is efficient for translocating inhaled Mn oxide as solid UFPs to the central nervous system and that this can result in inflammatory changes. We suggest that despite differences between human and rodent olfactory systems, this pathway is relevant in humans.

Abstract  Global warming is predicted to be most pronounced at high latitudes, and observational evidence over the past 25 years suggests that this warming is already under way. One-third of the global soil carbon pool is stored in northern latitudes, so there is considerable interest in understanding how the carbon balance of northern ecosystems will respond to climate warming. Observations of controls over plant productivity in tundra and boreal ecosystems have been used to build a conceptual model of response to warming, where warmer soils and increased decomposition of plant litter increase nutrient availability, which, in turn, stimulates plant production and increases ecosystem carbon storage. Here we present the results of a long-term fertilization experiment in Alaskan tundra, in which increased nutrient availability caused a net ecosystem loss of almost 2,000 grams of carbon per square meter over 20 years. We found that annual aboveground plant production doubled during the experiment. Losses of carbon and nitrogen from deep soil layers, however, were substantial and more than offset the increased carbon and nitrogen storage in plant biomass and litter. Our study suggests that projected release of soil nutrients associated with high-latitude warming may further amplify carbon release from soils, causing a net loss of ecosystem carbon and a positive feedback to climate warming.

Abstract  Relatively high deposition of nitrogen (N) in the northeastern United States has caused concern because sites could become N saturated. In the past, mass-balance studies have been used to monitor the N status of sites and to investigate the impact of increased N deposition. Typically, these efforts have focused on dissolved inorganic forms of N (DIN = NH_4-N + NO_3-N) and have largely ignored dissolved organic nitrogen (DON) due to difficulties in its analysis. Recent advances in the measurement of total dissolved nitrogen (TDN) have facilitated measurement of DON as the residual of TDN - DIN. We calculated DON and DIN budgets using data on precipitation and streamwater chemistry collected from 9 forested watersheds at 4 sites in New England. TDN in precipitation was composed primarily of DIN. Net retention of TDN ranged from 62 to 89% (4.7 to 10 kg ha^minus 1 yr^minus 1) of annual inputs. DON made up the majority of TDN in stream exports, suggesting that inclusion of DON is critical to assessing N dynamics even in areas with large anthropogenic inputs of DIN. Despite the dominance of DON in streamwater, precipitation inputs of DON were approximately equal to outputs. DON concentrations in streamwater did not appear significantly influenced by seasonal biological controls, but did increase with discharge on some watersheds. Streamwater NO_3-N was the only fraction of N that exhibited a seasonal pattern, with concentrations increasing during the winter months and peaking during snowmelt runoff. Concentrations of NO_3-N varied considerably among watersheds and are related to DOC:DON ratios in streamwater. Annual DIN exports were negatively correlated with streamwater DOC:DON ratios, indicating that these ratios might be a useful index of N status of upland forests.

Abstract  As part of the Lake Champlain Basin watershed study of mercury (Hg) and pollutant deposition, cloud water and cloud throughfall collections were conducted at the south summit (1204 m) of Mt. Mansfield, Vermont between August 1 and October 31, 1998, for multi-element chemical analysis. A passive Teflon string collector was deployed during non-precipitating events to sample cloud/fog water at timberline, while three sets of paired funnels collected cloud throughfall under the red spruce-balsam fir canopy. Samples were analyzed for concentrations of Hg, major ions, and 10 trace elements. Ultra-clean sampling and analysis techniques were utilized throughout the study. Six events were sampled for cloud water alone and four events were sampled for both cloud water and cloud throughfall. Cloud throughfall chemistry showed substantial modification from incident cloud water. Much higher concentrations of Hg (2.3 x), base cations (Ca2+, K-, Mg2+; 3-18 x) and certain trace elements (Ni, Cu, Mn, Rb, Sr; 2-34 x) were observed in throughfall than in cloud water. These results confirm that cloud water can leach a wide variety of elements from tree foliage and wash off dry deposited elements. Cloud water deposited an average of 0.42 +/- 0.12 mm of water per hour. Estimated cloud water deposition of Hg was 7.4 microg m(-2) for the period August 1-October 31, approximately twice that deposited by rain during this period at a nearby low elevation Hg monitoring site. Our results indicate that cloud water and Hg deposition at Mt. Mansfield are likely to have considerable ecological effects.

Abstract  Nitric oxides (NOx) play a very important role among the anthropogenic trace gases. They affect human health and have an impact on ozone chemistry and climatic change. Here we describe a new method for the quantification of the global NOx budget from image sequences of the Global Ozone Monitoring Experiment (GOME) spectrometer on board the ERS 2 satellite. In contrast to measurements using ground-based or balloon- or aircraft-borne sensors, this instrument provides, for the first time, the possibility of observing global maps of NO2 column densities. As part of this work, algorithms were developed to analyze GOME spectra numerically and to extract physically relevant parameters from the resulting maps using image-processing techniques. Column densities of NO, were determined using differential optical absorption spectroscopy (DOAS) [Platt, 1994]. By the combined use of an efficient B-spline interpolation and an inversion algorithm based on Householder transformations, the numerical algorithms accelerate the retrievals by a factor of 26 with respect to previous methods. Moreover, techniques are presented for separating tropospheric and stratospheric NO2 colums and estimating the lifetime of NO2 in the troposphere. This allows determination of regional NOx source strengths. Independent of traditional methods, a global source strength of (43 +/- 20) Tg N yr(-1) is estimated. The accurarcy of this method is comparable to that of established statistical aroaches.

Abstract  Nitrous acid is a significant photochemical precursor of the hydroxyl radical the key oxidant in the degradation of most air pollutants in the troposphere. The sources of nitrous acid in the troposphere, however, are still poorly understood. Recent atmospheric measurements revealed a strongly enhanced formation of nitrous acid during daytime via unknown mechanisms. Here we expose humic acid films to nitrogen dioxide in an irradiated tubular gas flow reactor and find that reduction of nitrogen dioxide on light-activated humic acids is an important source of gaseous nitrous acid. Our findings indicate that soil and other surfaces containing humic acid exhibit an organic surface photochemistry that produces reductive surface species, which react selectively with nitrogen dioxide. The observed rate of nitrous acid formation could explain the recently observed high daytime concentrations of nitrous acid in the boundary layer, the photolysis of which accounts for up to 60 per cent of the integrated hydroxyl radical source strengths. We suggest that this photo-induced nitrous acid production on humic acid could have a potentially significant impact on the chemistry of the lowermost troposphere.

Abstract  Epidemiological studies have found negative associations between human health and particulate matter in urban air. In most studies outdoor monitoring of urban background has been used to assess exposure. In a field study, personal exposure as well as bedroom, front door and background concentrations of PM(2.5), black smoke (BS), and nitrogen dioxide (NO(2)) were measured during 2-day periods in 30 subjects (20-33 years old) living and studying in central parts of Copenhagen. The measurements were repeated in the four seasons. Information on indoor exposure sources such as environmental tobacco smoke (ETS) and burning of candles was collected by questionnaires. The personal exposure, the bedroom concentration and the front door concentration was set as outcome variable in separate models and analysed by mixed effect model regression methodology, regarding subject levels as a random factor. Seasons were defined as a dichotomised grouping of outdoor temperature (above and below 8 degrees C). For NO(2) there was a significant association between personal exposure and both the bedroom, the front door and the background concentrations, whereas for PM(2.5) and BS only the bedroom and the front door concentrations, and not the background concentration, were significantly associated to the personal exposure. The bedroom concentration was the strongest predictor of all three pollution measurements. The association between the bedroom and front door concentrations was significant for all three measurements, and the association between the front door and the background concentrations was significant for PM(2.5) and NO(2), but not for BS, indicating greater spatial variation for BS than for PM(2.5) and NO(2). For NO(2), the relationship between the personal exposure and the front door concentration was dependent upon the "season", with a stronger association in the warm season compared with the cold season, and for PM(2.5) and BS the same tendency was seen. Time exposed to burning of candles was a significant predictor of personal PM(2.5), BS and NO(2) exposure, and time exposed to ETS only associated with personal PM(2.5) exposure. These findings imply that the personal exposure to PM(2.5), BS and NO(2) depends on many factors besides the outdoor levels, and that information on, for example, time of season or outdoor temperature and residence exposure, could improve the accuracy of the personal exposure estimation.

Abstract  Nitrogen oxides are trace gases that critically affect atmospheric chemistry and aerosol formation1. Vegetation is usually regarded as a sink for these gases, although nitric oxide and nitrogen dioxide have been detected as natural emissions from plants2, 3. Here we use in situ measurements to show that solar ultraviolet radiation induces the emission of nitrogen oxide radicals (NOx) from Scots pine (Pinus sylvestris) shoots when ambient concentrations drop below one part per billion. Although this contribution is insignificant on a local scale, our findings suggest that global NOx emissions from boreal coniferous forests may be comparable to those produced by worldwide industrial and traffic sources.

Abstract  Background: Acute myocardial infarction (AMI) is the leading cause of death attributed to cardiovascular diseases. An association between traffic-related air pollution and AMI has been suggested, but the evidence is still limited. Objectives: to evaluate in a multi-centre study association between hospitalisation for first AMI and daily levels of traffic-related air pollution. Methods: We collected data on first AMI hospitalisations in 5 European cities. AMI registers were available in Augsburg and Barcelona; hospital discharge registers (HDRs) were used in Helsinki, Rome and Stockholm. NO2, CO and PM10 (particles <10 mu m) were measured at central monitoring sites. Particle number concentration (PNC), a proxy for ultrafine particles (<0.1 mu m), was measured for a year in each centre, and then modelled retrospectively for the whole study period. We used generalized additive models for statistical analyses. Age and 28-day fatality and season were considered as potential effect modifiers in the 3 HDR centres. Results: Nearly 27 000 cases of first AMI were recorded. There was a suggestion of an association of the same day CO and PNC levels with AMI: RR=1.005 (95% confidence interval: 1.000-1.010) per 0.2 mg/m3 and RR=1.005 (95%CI: 0.996-1.015) per 10000 particles/cm3, respectively. However, associations were only observed in the 3 cities with HDR, where power for city-specific analyses was higher. We observed in these cities the most consistent associations among fatal cases aged <75 years: RR at 1-day lag for CO=1.021 (95%CI: 1.000-1.048) per 0.2 mg/m3, for PNC= 1.058 (95% CI: 1.012-1.107) per 10000 particles/cm3, and for NO2=1.032 (95%CI: 0.998-1.066) per 8 mu g/m3. Effects of air pollution were more pronounced during the warm than the cold season. Conclusions: We found support for the hypothesis that exposure to traffic-related air pollution increases the risk of AMI. Most consistent associations were observed among fatal cases aged <75 years and in the warm season.

Abstract  #BACKGROUND: Cohort studies have reported increased risks of cardiopulmonary mortality from long-term air pollution exposure, but the evidence is limited and inconclusive. We studied the association between long-term exposure to source-specific air pollution and myocardial infarction (MI) in a case-control study of first-time MI cases and population controls age 45 to 70 years in Stockholm county in 1992 to 1994. METHODS: Home addresses during several decades were combined with historical emission databases and dispersion models to obtain annual mean levels of pollutants from traffic and heating during 30 years for 1397 cases and 1870 controls. Nitrogen dioxide (NO2), carbon monoxide (CO), and particulate matter with an aerodynamic diameter less than 10 microm (PM10) were used as indicators of traffic emissions and sulfur dioxide (SO2) as an indicator of emissions from residential heating. RESULTS: There was no association between long-term average air pollution exposure and overall MI, but an increased risk of fatal MI was suggested, especially for out-of-hospital death. After adjustment for cardiovascular risk factors, the odds ratio for fatal MI associated with a 5th to 95th percentile difference in 30-year average exposure was 1.51 (95% confidence interval = 0.96-2.16) for NO2, 1.22 (0.98-1.52) for CO, 1.39 (0.94-2.07) for PM10, and 1.24 (0.77-2.02) for SO2. For out-of-hospital death, the odds ratio related to NO2 exposure was 2.17 (1.05-4.51). CONCLUSIONS: This study provides some support for an association between long-term air pollution exposure and fatal cardiovascular disease.

Abstract  BACKGROUND: Living close to major roads or highways has been suggested to almost double the risk of dying from cardiopulmonary causes. We assessed whether long-term exposure to air pollution originating from motorized traffic and industrial sources is associated with total and cause-specific mortality in a cohort of women living in North Rhine-Westphalia, Germany. METHODS: The study was a follow-up of a series of cross-sectional studies carried out during the 1980s and 1990s on the health of women (age 50-59 years). Approximately 4800 women were followed up for vital status and migration. Exposure to air pollution was defined by distance to major roads calculated from Geographic Information System data and by 1- and 5-year average nitrogen dioxide (NO2) and particle (PM10) concentrations calculated from air monitoring station data. We analyzed associations between exposure and mortality using Cox's proportional hazards models adjusting for confounders. Relative risks (RRs) refer to an interquartile range increase in exposure (16 microg/m for NO2; 7 microg/m for PM10). RESULTS: During the follow-up period, 8% of the women died, 3% from cardiopulmonary causes. Cardiopulmonary mortality was associated with living within a 50-meter radius of a major road (adjusted RR = 1.70; 95% confidence interval = 1.02-2.81), with NO2 (1.57; 1.23-2.00 for 1-year average), and with PM10 (1.34; 1.06-1.71 for 1-year average). Exposure to NO2 was also associated with all-cause mortality (1.17; 1.02-1.34). No association was seen with noncardiopulmonary nonlung cancer mortality. CONCLUSIONS: Living close to major roads and chronic exposure to NO2 and PM10 may be associated with an increased mortality due to cardiopulmonary causes.

Abstract  In the past few years many studies on air pollution and health based on time series have been carried out. Yet, this approach does not assess exposure to air pollution at an individual level but it is based on ambient concentrations measured by air quality monitoring networks. Questions on the estimates of exposure to pollutants have been raised, in particular the fact that background measuring stations only have been considered in the set up of pollution indicators. To assess the impact of exposure indicator characteristics on the results of time series analysis, two series (black smoke and sulfur dioxide, respectively) of exposure indicators to urban air pollution were set up taking into account a growing part of proximity measures (industrial sources) available in the studied urban area (Le Havre, France). For each pollutant, indicators distributions were almost similar, especially for black smoke. Whatever the pollutant, the most obvious heterogeneity could be observed between the 100% background indicator and the indicator including the arithmetic mean for all the stations (50% background stations and 50% proximity stations). Then the sensitivity of the associations between mortality and air pollution to these indicators was studied. These indicators did not show statistically significant differences in the estimated excess risk. Yet, confidence intervals were more statistically significant as the contribution of proximity stations was more substantial, in particular for SO2. To conclude, the use of proximity measurements did not influence dramatically on the mean estimates of the association between air pollution and mortality indicators in Le Havre. Therefore it does not seem relevant to include the data provided by the proximity stations in the urban exposure indicators within the context of the epidemiology monitoring system.

Abstract  Epidemiological studies to evaluate the acute effects of ambient SO2 on the respiratory health of children provide inconclusive results. A panel study to examine the association of short-term exposure to ambient SO2 and respiratory symptoms of 196 children for a period of 107 days was conducted in Thailand. Generalized Estimating Equations were used to examine the association of daily variation of air pollution with daily respiratory symptoms. During the study period, SO2 was not associated with respiratory symptoms in either asthmatics or non-asthmatics, whereas a 10 microg/m3 increase in PM10 was modestly associated with increases of lower respiratory symptom incidence (OR=1.03, 95%CI=0.98, 1.09) and cough (OR=1.04, 95% CI=1.00, 1.08) in asthmatics. At the low ambient air pollution concentrations observed, particulate matter rather than SO2 was associated on a microg/m3 basis with acute daily respiratory symptoms.

Abstract  The American Cancer Society (ACS) Study and its reanalysis are built upon in order to examine the impact of scale on the observed relationship between sulfates and mortality. The limitations of the original ACS Study (Pope et al., 1995) and the reanalysis of this study (Krewski et al., 2000) are discussed; while the latter dealt with some issues in using ecological data, it did not address scale. Next, the article outlines the county-scale study, the methods used to aggregate data, and the two-stage analysis used to derive relative risk (RR). Finally, the results of working at the county scale are compared with those obtained by the reanalysis team using larger metropolitan areas. Less than half of the cohort used in the metropolitan study were used at the county scale because of the limited availability of sulfate monitors and because five-digit ZIP codes more accurately assigned individuals to geographical areas. Therefore, the county data should be considered as new and not as a reorganization of the original data set. The reanalysis and the county studies should be considered as two separate studies that took different scales as their basic organizing principle. The RR of all-cause mortality from sulfate exposure at the county scale was 1.50 (1.30, 1.73) compared with 1.25 (1.13, 1.37) at the metropolitan scale; for cardiopulmonary mortality, the RR was 1.75 (1.48, 2.08) at the county scale compared with 1.29 (1.15, 1.46) at the metropolitan scale. Because lung cancer mortality was low in some counties, the two-stage random effects model became unstable. At the county scale, the RR from sulfates was more robust to the inclusion of ecologic covariates. Other place-specific ecologic covariates were either insignificant or barely significant (with a lower 95% confidence limit near 0.99 or 1.00) when included in the two-stage regression model for all-cause mortality with sulfates. Moreover, no ecologic covariate changed the RR of all-cause mortality from sulfates by 25% or more. Both population change and unemployment rate affected the RR for cardiopulmonary mortality from sulfate exposure by 25% or more in the county-scale analysis. However, when these two variables were entered into a multiple covariate analysis, the RR from sulfates decreased but remained strongly significant. Sulfur dioxide was not an important covariate at the county scale. Thus, at the county scale, long-term exposure to sulfates appears to be more strongly associated with increased risk of all-cause and cardiopulmonary mortality than previously indicated by the ACS study and its reanalysis.

Abstract  #In 1995, daily mortality in a district of Chongqing, China, was analyzed from January through December for associations with daily ambient sulfur dioxide and fine particles (airborne particles with diameters less than or equal to 2.5 microm; PM2.5. The mean concentration of PM2.5 was 147 microg/m3 (maximum, 666 microg/m3), and that of SO2 was 213 microg/m3 (maximum, 571 microg/m3). On average, 9.6 persons died each day. We used a generalized additive model using robust Poisson regression to estimate the associations of mean daily SO2 and PM2.5 with daily mortality (on the same day and at lags up to 5 days) adjusted for trend, season, temperature, humidity, and day of the week. The relative risk of mortality associated with a 100 microg/m3 increase in mean daily SO2 was highest on the second lag day [1.04; 95% confidence interval (CI), 1.00-1.09] and the third lag day (1.04; 95% CI, 0.99-1.08). The associations between daily mortality and mean daily PM2.5 were negative and statistically insignificant on all days. The relative risk of respiratory mortality on the second day after a 100 microg/m3 increase in mean daily SO2 was 1.11 (95% CI, 1.02-1.22), and that for cardiovascular mortality was 1.10 (95% CI, 1.02-1.20). The relative risk of cardiovascular mortality on the third day after a 100 microg/m3 increase in mean daily SO2 was 1.20 (95% CI, 1.11-1.30). The relative risks of mortality due to cancer and other causes were insignificant on both days. The estimated effects of mean daily SO2 on cardiovascular and respiratory mortality risk remained after controlling for PM2.5.

Abstract  Until recently, urban air quality modelling has been based on operational models of an integral nature. The use of computational fluid dynamics (CFD) models to address the same problems is increasing rapidly. Operational models e.g. OSPM, AERMOD, ADMS-Urban have undergone many comprehensive formal evaluations as to their "fitness for purpose" while CFD models do not have such an evaluation record in the urban air quality context. This paper looks at the application of both approaches to common problems. In particular, pollutant dispersion from point and line sources in the simplest neutral atmospheric boundary layer and line sources placed within different regular building geometries is studied with the CFD code FLUENT and the atmospheric dispersion model ADMS-Urban. Both the effect of street canyons of different aspect ratios and various obstacle array configurations consisting of cubical buildings are investigated. The standard k-epsilon turbulence model and the advection-diffusion (AD) method (in contrast to the Lagrangian particle tracking method) are used for the CFD simulations. Results from the two approaches are compared. Overall CFD simulations with the appropriate choice of coefficients produce similar concentration fields to those predicted by the integral approach. However, some quantitative differences are observed. These differences can be explained by investigating the role of the Schmidt number in the CFD simulations. A further interpretation of the differences between the two approaches is given by quantifying the exchange velocities linked to the mass fluxes between the in-canopy and above-canopy layers. (c) 2007 Elsevier Ltd. All rights reserved.

Abstract  Water-soluble organic compounds (WSOC) in size-segregated aerosol samples, cloud water and wet depositions collected at Jeju Island during the ACE-Asia experiment were characterized in terms of main functional groups and chemical classes by means of liquid chromatography coupled with total organic carbon (TOC) analysis, and by nuclear magnetic resonance (NMR) spectroscopy. The surface-active character of the WSOC was also deduced by measuring the surface tension (ST) of cloud water, wet depositions and aerosol water-extracts as a function of WSOC concentration. WSOC in the size-segregated aerosol samples at the Kosan coastal site show the occurrence of oxidized species, enriched in the accumulation mode, and a functional group composition characteristic of continental industrialized areas, with a small impact from biomass burning sources. The chemical classes identified and quantified by liquid chromatography accounted for 88% of the water-soluble organic carbon on average. The relatively high proportion of polycarboxylic acids (PA, 33-40% of total characterized WSOC) observed throughout the campaign indicates the persistence of WSOC from continental pollution sources in air masses which spent up to 5 days in the marine boundary layer (MBL) of the Yellow Sea. The analysis of cloud water and wet depositions collected at a mountain site in Jeju shows substantial differences in the organic composition between the cloud/rainwater solutes and the water-soluble fraction of the aerosol at the coastal site, with PA acids contributing to cloud water WSOC in far smaller proportions (6-11%) than in the fine MBL aerosols. It was proposed that such differences resulted from the entrainment of aerosol particles from the lifted layers into the stratiform clouds. Following this hypothesis, the saturated aliphatic compounds determined by NMR analysis in the rainwater samples, which are also responsible for the observed significant ST lowering, were scavenged above the boundary layer and had possibly been transported from the continent in the lifted layers. The hypothesized features of the vertical profiles in the inorganic and organic aerosol chemical composition are in agreement with the results of aircraft-based measurements performed during the same experiment. (C) 2004 Elsevier Ltd. All rights reserved.

Abstract  Background Airborne particulate matter (PM) is an important factor associated with the enhanced prevalence of respiratory allergy. The PM adjuvant activity on allergic sensitization is a possible mechanism of action involved, and the induction of airway inflammation is suggested to be of importance in PM-induced adjuvant activity. Objective Because differently sized PM have different toxic potentials, we studied the role of particle size in the induction of airway inflammation and allergic sensitization. This was done using fine (0.250 and 0.260 μm) and ultrafine (0.029 and 0.014 μm) titanium dioxide (TiO2) and carbon black particles (CBP) with known differences in airway toxicity. Methods Mice were intranasally exposed to ovalbumin (OVA) alone or in combination with one of the different particles. The induction of airway inflammation and the immune adjuvant activity were studied in the lungs and lung-draining peribronchial lymph nodes (PBLN) at day 8. OVA-specific antibodies were measured at day 21, and the development of allergic airway inflammation was studied after OVA challenges (day 28). Results When administered at the same total particle mass (200 μg), exposure to ultrafine TiO2 and CBP-induced airway inflammation, and had immune adjuvant activity. The latter was shown by increasing both the PBLN cell numbers and the production of OVA-specific T-helper type 2 (Th2) cytokines (IL-4, IL-5, IL-10 and IL-13). Whereas OVA-specific IgE and IgG1 levels in serum were only increased in animals exposed to the ultrafine TiO2, allergic airway inflammation could be detected in both ultrafine TiO2-and CBP-treated groups after challenges with OVA. Conclusion Our data show that only the ultrafine particles, with a small diameter and a large total surface area/mass, cause airway inflammation and have immune adjuvant activity in the current model supporting the hypothesis that particle toxicity is site-dependent and related to adjuvant activity.

Abstract  Multi-element simultaneous electrothermal atomic absorption spectrometry (ETAAS) methods were developed for determining 11 elements, in three analytical groups (group-1, predominately crustal elements, Al, Cu, Fe, Mn, and Cr; group-2, tracers of coal and oil combustion as well as other anthropogenic sources, Se, As, Pb, and Ni; and group-3, tracers of municipal incinerator aerosol–Zn and Cd), in aqueous slurry of ambient fine airborne particles, collected, at 30 min intervals with the University of Maryland–Semicontinuous Elements in Aerosol Sampler-II (SEAS-II). Combined effects of acid (0.2% v/v nitric acid) and ultrasonic treatment (15 min) improved metals recovery and slurry stability. Linear calibration ranges were improved by using a 50 mL min−1 carrier gas flow (mini-flow) during the atomization stage. However, analytical sensitivity for group-1 and 3 elements was compromised. Palladium (4 μg) and hydrogen (5% in Argon) were found to be effective modifiers for group-1 and 2 elements. A fast furnace temperature program was developed for group-3. Detection limits for the eleven marker elements by the SEAS-II-ETAA approach were compared with traditional filter X-ray fluorescence, laser ablation-ICPMS, and instrumental neutron activation analysis (INAA) techniques used in air quality studies. The efficacy of the analytical method was evaluated by analyzing interim urban PM2.5 reference material, collected in Baltimore, by the National Institute of Standards and Technology (NIST) Gaithersburg, MD. Results obtained by the ETAAS methods agreed well with the results obtained by NIST using INAA.