Jc. Chow et al., Temporal variations of PM2.5, PM10, and gaseous precursors during the 1995integrated monitoring study in central California, J AIR WASTE, 49, 1999, pp. 16-24
Citations number
20
Categorie Soggetti
Environment/Ecology,"Environmental Engineering & Energy
The spatial and temporal distributions of particle mass and its chemical co
nstituents are essential for understanding the source-receptor relationship
s as well as the chemical, physical, and meteorological processes that resu
lt in elevated particulate concentrations in California's San Joaquin Valle
y (SJV). Fine particulate matter (PM2.5), coarse particulate matter (PM10),
and aerosol precursor gases were sampled on a 3-hr time base at two urban
(BakersfieId and Fresno) and two non-urban (Kern Wildlife Refuge and Chowch
illa) core sites in the SJV during the winter of 1995-1996.
Day-to-day variations of PM2.5 and PM10 and their chemical constituents wer
e influenced by the synoptic-scale meteorology and were coherent among the
four core sites. Under non-rainy conditions, similar diurnal variations of
PM2.5 and coarse aerosol were found at the two urban sites, with concentrat
ions peaking during the nighttime hours. Conversely, PM2.5 and coarse aeros
ol peaked during the morning and afternoon hours at the two nonurban sites.
Under rainy and foggy conditions, these diurnal patterns were absent or gr
eatly suppressed.
In the urban areas, elevated concentrations of primary pollutants (e.g., or
ganic and elemental carbons) during the late afternoon and nighttime hours
reflected the impact from residential wood combustion and motor vehicle exh
aust. During the daytime, these concentrations decreased as the mixed layer
deepened. Increases of secondary nitrate and sulfate concentrations were f
ound during the daylight hours as a result of photochemical reactions. At t
he non-urban sites, the same increases in secondary aerosol concentrations
occurred during the daylight hours but with a discernable lag time. Concent
rations of the primary pollutants also increased at the non-urban sites dur
ing the daytime. These observations are attributed to mixing aloft of prima
ry aerosols and secondary precursor gases in urban areas followed by rapid
transport aloft to non-urban areas coupled with photochemical conversion.