the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Summertime contributions of isoprene, monoterpenes, and sesquiterpene oxidation to the formation of secondary organic aerosol in the troposphere over Mt. Tai, Central East China during MTX2006
Abstract. To better understand the contribution of biogenic volatile organic compounds to the formation of secondary organic aerosol (SOA) in high mountain regions, ambient aerosols were collected at the summit of Mt. Tai (1534 m, a.s.l.), Central East China (CEC) during the Mount Tai eXperiment 2006 campaign (MTX2006) in early summer. Biogenic SOA tracers of isoprene, monoterpenes, and β-caryophyllene oxidation products were measured using gas chromatography/mass spectrometry. All the biogenic SOA tracers showed no clear diurnal variations, suggesting that they are formed during long-range atmospheric transport. Although isoprene- and monoterpene-derived SOA tracers did not correlate with levoglucosan (a biomass burning tracer), β-caryophyllinic acid showed a good correlation with levoglucosan, indicating that biomass burning may be a source for this compound. Total concentrations of isoprene oxidation products are much higher than those of monoterpene and β-caryophyllene oxidation products. The ratio of isoprene to monoterpene oxidation products (Riso/mono) was found to co-vary with ozone and NOx during the summer campaign. The average Riso/mono value was 6.94 at daytime and 10.0 at nighttime. These values are among the highest in the aerosols studied in different regions, which may be due to the large isoprene fluxes, high O3 and NOx levels and relatively high OH concentrations in CEC. Using a tracer-based method, we estimated the average concentrations of secondary organic carbon (SOC) derived from isoprene, monoterpenes, and β-caryophyllene to be 1.76 μgC m−3 at daytime and 1.85 μgC m−3 at nighttime. These values correspond to 11.2% and 11.0% of the total OC concentrations, in which isoprene-derived SOC are 7.4% and 8.0% at day- and night-time, respectively. This study suggests that isoprene is a more significant precursor for biogenic SOA than monoterpenes and β-caryophyllene in high altitude in CEC.
- Preprint
(1307 KB) - Metadata XML
- BibTeX
- EndNote
-
RC C5416: 'Review', Anonymous Referee #1, 30 Sep 2009
- AC C8829: 'Reply to Referee #1', Pingqing Fu, 22 Dec 2009
-
RC C5428: 'Review', Anonymous Referee #2, 30 Sep 2009
- AC C8830: 'Reply to Referee #2', Pingqing Fu, 22 Dec 2009
-
RC C5443: 'Review', Anonymous Referee #3, 01 Oct 2009
- AC C8835: 'Reply to Referee #3', Pingqing Fu, 22 Dec 2009
-
RC C5416: 'Review', Anonymous Referee #1, 30 Sep 2009
- AC C8829: 'Reply to Referee #1', Pingqing Fu, 22 Dec 2009
-
RC C5428: 'Review', Anonymous Referee #2, 30 Sep 2009
- AC C8830: 'Reply to Referee #2', Pingqing Fu, 22 Dec 2009
-
RC C5443: 'Review', Anonymous Referee #3, 01 Oct 2009
- AC C8835: 'Reply to Referee #3', Pingqing Fu, 22 Dec 2009
Viewed
HTML | XML | Total | BibTeX | EndNote | |
---|---|---|---|---|---|
953 | 925 | 149 | 2,027 | 147 | 139 |
- HTML: 953
- PDF: 925
- XML: 149
- Total: 2,027
- BibTeX: 147
- EndNote: 139
Cited
9 citations as recorded by crossref.
- Measurement of overall uptake coefficients for HO<sub>2</sub> radicals by aerosol particles sampled from ambient air at Mts. Tai and Mang (China) F. Taketani et al. 10.5194/acp-12-11907-2012
- Characterization of organic tracer compounds in PM2.5 at a semi-urban site in Beirut, Lebanon A. Waked et al. 10.1016/j.atmosres.2014.02.006
- Contribution of Primary and Secondary Sources to Organic Aerosol and PM2.5 at SEARCH Network Sites T. Kleindienst et al. 10.3155/1047-3289.60.11.1388
- Characteristics and contributions of biogenic secondary organic aerosol tracers to PM 2.5 in Shanghai, China W. Zhu et al. 10.1016/j.apr.2017.09.001
- Secondary organic aerosol characterisation at field sites across the United States during the spring–summer period M. Lewandowski et al. 10.1080/03067319.2013.803545
- Molecular characterization of urban organic aerosol in tropical India: contributions of primary emissions and secondary photooxidation P. Fu et al. 10.5194/acp-10-2663-2010
- Seasonal cycle and temperature dependence of pinene oxidation products, dicarboxylic acids and nitrophenols in fine and coarse air particulate matter Y. Zhang et al. 10.5194/acp-10-7859-2010
- Photo-oxidation products of α-pinene in coarse, fine and ultrafine aerosol: A new high sensitive HPLC-MS/MS method M. Feltracco et al. 10.1016/j.atmosenv.2018.02.052
- PTR-MS measurements of non-methane volatile organic compounds during an intensive field campaign at the summit of Mount Tai, China, in June 2006 S. Inomata et al. 10.5194/acp-10-7085-2010