Continuous measurements of particle number (PN), particle mass (PM 10 ), and gaseous pollutants [carbon monoxide (CO), nitric oxide (NO), oxides of nitrogen (NO x ), and ozone (O 3 )] were performed at five urban sites in the Los Angeles Basin to support the University of Southern California Children's Health Study in 2002. The degree of correlation between hourly PN and concentrations of CO, NO, and nitrogen dioxide (NO 2 ) at each site over the entire year was generally low to moderate (r values in the range of 0.1-0.5), with a few notable exceptions. In general, associations between PN and O 3 were either negative or insignificant. Similar analyses of seasonal data resulted in levels of correlation with large variation, ranging from 0.0 to 0.94 depending on site and season. Summertime data showed a generally higher correlation between the 24-hr average PN concentrations and CO, NO, and NO 2 than corresponding hourly concentrations. Hourly correlations between PN and both CO and NO were strengthened during morning rush-hour periods, indicating a common vehicular source. Comparing hourly particle number concentrations between sites also showed low to moderate spatial correlations, with most correlation coefficients below 0.4. Given the low to moderate associations found in this study, gaseous co-pollutants should not be used as surrogates to assess human exposure to airborne particle number concentrations.
INTRODUCTIONRecent research has demonstrated that numerous adverse health outcomes are associated with atmospheric particulate matter (PM). Epidemiologic studies have shown significant relationships between ambient PM and respiratoryrelated mortality and morbidity. 1,2 The observed effects are even more significant in susceptible populations, such as the elderly, with pre-existing respiratory and cardiovascular diseases. 3 Toxicological studies by Oberdorster 4 and Donaldson et al. 5 have concluded that ultrafine particles (particles with diameters less than ϳ100 nm) are comparatively more toxic than larger particles with identical chemical composition and mass. Because of their small size, ultrafine particles contribute very little to the overall PM mass but comprise a significant majority of the number of airborne particles in the atmosphere. 3,6 It is still unknown whether the observed PM health effects are related to particle number (PN), particle surface area, particle mass, or particle chemical composition. Studies on rodents show that inflammatory response is more prominent when ultrafine particles are administered compared with larger particles, 3 suggesting either a particle number or surface area effect. Toxicological studies also have shown that ultrafine particles have higher oxidative stress potential and can penetrate and destroy mitochondria within epithelial cells. 7 Penttinen et al. 8 tested the hypothesis that high numbers of ultrafine particles in the atmosphere can induce alveolar inflammation and exacerbation of pre-existing cardiopulmonary diseases. They found that daily mean num...