• Journal of Korean Society for Atmospheric Environment
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• v.32 no.2
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• pp.208-215
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• 2016

Pinic acid (PA) and cis-pinonic acid (CPA) in the atmospheric particulate matter with an aerodynamic diameter of less than or equal to a nominal $10{\mu}m$ ($PM_{10}$) were analyzed for the samples collected during the period of April 2010 to April 2011 at Jongro in Seoul. Both pinic acid and cis-pinonic acid showed higher seasonal average concentrations in summer (PA; $18.9ng/m^3$, CPA; $16.0ng/m^3$) than winter (PA; $5.3ng/m^3$, CPA; $5.9ng/m^3$). They displayed a seasonal pattern associated with temperature reflecting the influence on emissions of ${\alpha}-pinene$ and ${\beta}-pinene$ from conifers and their photochemical reaction. These results were confirmed through Pearson correlation coefficient between CPA, PA and $O_3+NO_2$, temperature. CPA was only correlated with n-alkanes ($C_{29}$, $C_{31}$, $C_{33}$) from biogenic source. PA was correlated with n-alkanes ($C_{29}$, $C_{31}$, $C_{33}$), n-alkanoic acid ($C_{20}$, $C_{22}$, $C_{24}$) from biogenic source and n-alkanes ($C_{28}$, $C_{30}$, $C_{32}$), and n-alkanoic acid ($C_{16}$, $C_{18}$) from anthropogenic source. These results showed that the formation of PA and CPA from ${\alpha}-pinene$ and ${\beta}-pinene$ is related to organic compounds from biogenic source. And it is possible for PA to be effected by organic compounds from anthropogenic source.

• Asian Journal of Atmospheric Environment
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• v.11 no.3
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• pp.165-175
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• 2017

In Japan, the primary carbonaceous particles emitted from motor vehicles and waste incinerators have been reduced due to strict regulations against exhaust gas. However, the relative contribution of carbonaceous particles derived from plants and biomass has been increasing. Accordingly, compositional analysis of carbonaceous particles has become increasingly important to determine the sources and types of particles produced. To reveal the sources of the organic particles contained in particulate matter with diameters of ${\leq}2.5{\mu}m$ ($PM_{2.5}$) and the processes involved in their generation, we analyzed molecular marker compounds (2-methyltetrols, cis-pinonic acid, and levoglucosan) derived from the plants and biomass in the $PM_{2.5}$ collected during daytime- and nighttime-sampling periods in summer (July and August) and autumn (November) in Kazo, which is in the northern area of Saitama prefecture, Japan. We also measured $^{14}C$ carbonaceous concentrations in the same $PM_{2.5}$ samples. The concentrations of 2-methyltetrols were higher in the summer than in the autumn. Because the deciduous period overlaps with this decrease in the levels of 2-methyltetrols, we considered the emission source to broad-leaved trees. In contrast, the emission source of the cis-pinonic acid precursor was considered to be conifers, because its concentration remained almost constant throughout the year. The concentration of levoglucosan was considerably increased in the autumn due to frequent biomass open burning. The ratio of plant-derived carbon to total carbon, obtained by measuring of $^{14}C$, in summer $PM_{2.5}$ sample was higher in the nighttime, and could be influenced by anthropogenic sources during the daytime.