TY - JOUR
T1 - Spatial variations of PM2.5 during the Pittsburgh air quality study
AU - Tang, Wei
AU - Raymond, Timothy
AU - Wittig, Beth
AU - Davidson, Cliff
AU - Pandis, Spyros
AU - Robinson, Allen
AU - Crist, Kevin
N1 - Funding Information:
This research was conducted as part of the Pittsburgh Air Quality Study, which was supported by US Environmental Protection Agency under contract R82806101 and the US Department of Energy National Energy Technology Laboratory under contract DE-FC26-01NT41017. This article has not been subject to the EPA’s peer and policy review, and therefore does not necessarily reflect the views of the Agency. No official endorsement should be inferred.
PY - 2004/10
Y1 - 2004/10
N2 - Measurements of 24 h PM2.5 total mass, sulfate, ammonium, and organic carbon show similar concentrations within experimental error at six sampling locations separated by more than 300 km. The measurements were obtained during summer 2001 in the center of Pittsburgh as well as in less-populated areas upwind and down-wind of the city. Measurable differences among the six sites were observed for nitrate and elemental carbon during the same time period. In contrast, measurable differences were observed for total mass and all five chemical species at the same sites during winter 2002. The results suggest that concentrations may be remarkably uniform over large areas due to secondary aerosol production from gases emitted in upwind areas. Meteorological back-trajectories show that concentrations can steadily increase along an airmass trajectory, and that regions downwind of a city such as Pittsburgh may be affected by city emissions; however, PM2.5 levels measured within the city may not be significantly affected by local emissions if background levels are sufficiently high.
AB - Measurements of 24 h PM2.5 total mass, sulfate, ammonium, and organic carbon show similar concentrations within experimental error at six sampling locations separated by more than 300 km. The measurements were obtained during summer 2001 in the center of Pittsburgh as well as in less-populated areas upwind and down-wind of the city. Measurable differences among the six sites were observed for nitrate and elemental carbon during the same time period. In contrast, measurable differences were observed for total mass and all five chemical species at the same sites during winter 2002. The results suggest that concentrations may be remarkably uniform over large areas due to secondary aerosol production from gases emitted in upwind areas. Meteorological back-trajectories show that concentrations can steadily increase along an airmass trajectory, and that regions downwind of a city such as Pittsburgh may be affected by city emissions; however, PM2.5 levels measured within the city may not be significantly affected by local emissions if background levels are sufficiently high.
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U2 - 10.1080/02786820490442833
DO - 10.1080/02786820490442833
M3 - Article
AN - SCOPUS:2442437725
SN - 0278-6826
VL - 38
SP - 80
EP - 90
JO - Aerosol Science and Technology
JF - Aerosol Science and Technology
IS - SUPPL. 2
ER -