Atmospheric organic vapors in two European pine forests measured by a Vocus PTR-TOF: insights into monoterpene and sesquiterpene oxidation processes
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Published:2021-03-18
Issue:5
Volume:21
Page:4123-4147
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ISSN:1680-7324
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Container-title:Atmospheric Chemistry and Physics
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language:en
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Short-container-title:Atmos. Chem. Phys.
Author:
Li HaiyanORCID, Canagaratna Manjula R., Riva MatthieuORCID, Rantala PekkaORCID, Zhang YanjunORCID, Thomas Steven, Heikkinen LiineORCID, Flaud Pierre-Marie, Villenave Eric, Perraudin Emilie, Worsnop Douglas, Kulmala MarkkuORCID, Ehn MikaelORCID, Bianchi FedericoORCID
Abstract
Abstract. Atmospheric organic vapors play essential roles in the formation of
secondary organic aerosol. Source identification of these vapors is thus
fundamental to understanding their emission sources and chemical evolution in the atmosphere and their further impact on air quality and climate change. In this study, a Vocus proton-transfer-reaction time-of-flight mass
spectrometer (PTR-TOF) was deployed in two forested environments, the Landes forest in southern France and the boreal forest in southern Finland, to measure atmospheric organic vapors, including both volatile organic
compounds (VOCs) and their oxidation products. For the first time, we
performed binned positive matrix factorization (binPMF) analysis on the
complex mass spectra acquired with the Vocus PTR-TOF and identified various
emission sources as well as oxidation processes in the atmosphere. Based on
separate analysis of low- and high-mass ranges, 15 PMF factors in the
Landes forest and nine PMF factors in the Finnish boreal forest were resolved, showing a high similarity between the two sites. Particularly,
terpenes and various terpene reaction products were separated into
individual PMF factors with varying oxidation degrees, such as lightly
oxidized compounds from both monoterpene and sesquiterpene oxidation,
monoterpene-derived organic nitrates, and monoterpene more oxidized
compounds. Factors representing monoterpenes dominated the biogenic VOCs in
both forests, with lower contributions from the isoprene factors and sesquiterpene factors. Factors of the lightly oxidized products, more oxidized products, and organic nitrates of monoterpenes/sesquiterpenes accounted for 8 %–12 % of the measured gas-phase organic vapors in the two forests. Based on the interpretation of the results relating to oxidation processes, further insights were gained regarding monoterpene and sesquiterpene reactions. For example, a strong relative humidity (RH) dependence was found for the behavior of sesquiterpene lightly oxidized compounds. High concentrations of these compounds only occur at high RH; yet similar behavior was not observed for monoterpene oxidation products.
Funder
H2020 European Research Council Academy of Finland
Publisher
Copernicus GmbH
Subject
Atmospheric Science
Reference99 articles.
1. Abis, L., Loubet, B., Ciuraru, R., Lafouge, F., Houot, S., Nowak, V.,
Tripied, J., Dequiedt, S., Maron, P. A., and Sadet-Bourgeteau, S.: Reduced
microbial diversity induces larger volatile organic compound emissions from
soils, Scient. Rep., 10, 6104, https://doi.org/10.1038/s41598-020-63091-8, 2020. 2. Ahlberg, E., Falk, J., Eriksson, A., Holst, T., Brune, W. H., Kristensson,
A., Roldin, P., and Svenningsson, B.: Secondary organic aerosol from VOC
mixtures in an oxidation flow reactor, Atmos. Environ., 161, 210–220,
https://doi.org/10.1016/j.atmosenv.2017.05.005, 2017. 3. Allan, B. J., McFiggans, G., Plane, J. M. C., Coe, H., and McFadyen, G. G.:
The nitrate radical in the remote marine boundary layer, J. Geophys.
Res.-Atmos., 105, 24191–24204, https://doi.org/10.1029/2000JD900314, 2000. 4. Baudic, A., Gros, V., Sauvage, S., Locoge, N., Sanchez, O., Sarda-Estève, R., Kalogridis, C., Petit, J.-E., Bonnaire, N., Baisnée, D., Favez, O., Albinet, A., Sciare, J., and Bonsang, B.: Seasonal variability and source apportionment of volatile organic compounds (VOCs) in the Paris megacity (France), Atmos. Chem. Phys., 16, 11961–11989, https://doi.org/10.5194/acp-16-11961-2016, 2016. 5. Bianchi, F., Tröstl, J., Junninen, H., Frege, C., Henne, S., Hoyle, C.
R., Molteni, U., Herrmann, E., Adamov, A., Bukowiecki, N., Chen, X., Duplissy, J., Gysel, M., Hutterli, M., Kangasluoma, J., Kontkanen, J.,
Kürten, A., Manninen, H. E., Münch, S., Peräkylä, O.,
Petäjä, T., Rondo, L., Williamson, C., Weingartner, E., Curtius, J.,
Worsnop, D. R., Kulmala, M., Dommen, J., and Baltensperger, U.: New particle
formation in the free troposphere: A question of chemistry and timing,
Science, 352, 1109–1112, https://doi.org/10.1126/science.aad5456, 2016.
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