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Contributions of individual reactive biogenic volatile organic compounds to organic nitrates above a mixed forest

Authors :
L. H. Mielke
M. Alaghmand
Christoph S. Vogel
Detlev Helmig
Allison L. Steiner
R. Daly
Philip S. Stevens
John Ortega
Kerri A. Pratt
Sebastien Dusanter
Stephen M. Griffith
A. M. Bryan
Paul B. Shepson
Purdue Climate Change Research Center
Purdue University [West Lafayette]
School of Information, University of Michigan
University of Michigan [Ann Arbor]
University of Michigan System-University of Michigan System
Fisica Aplicada II
Facultad de Ciencia y Tecnologia, Bilbao
inconnu
Inconnu
Institute of Arctic and Alpine Research (INSTAAR)
University of Colorado [Boulder]
Department of Medical Microbiology and Infectious Diseases
Erasmus University Medical Center [Rotterdam] (Erasmus MC)
École des Mines de Douai (Mines Douai EMD)
Institut Mines-Télécom [Paris] (IMT)
Department of Anthropology [Indiana University]
Indiana University [Bloomington]
Indiana University System-Indiana University System
Source :
Atmospheric Chemistry and Physics, Atmospheric Chemistry and Physics, 2012, Atmospheric Chemistry and Physics, Vol 12, Iss 21, Pp 10125-10143 (2012)
Publication Year :
2012
Publisher :
Copernicus GmbH, 2012.

Abstract

Biogenic volatile organic compounds (BVOCs) can react in the atmosphere to form organic nitrates, which serve as NOx (NO + NO2) reservoirs, impacting ozone and secondary organic aerosol production, the oxidative capacity of the atmosphere, and nitrogen availability to ecosystems. To examine the contributions of biogenic emissions and the formation and fate of organic nitrates in a forest environment, we simulated the oxidation of 57 individual BVOCs emitted from a rural mixed forest in northern Michigan. Key BVOC-oxidant reactions were identified for future laboratory and field investigations into reaction rate constants, yields, and speciation of oxidation products. Of the total simulated organic nitrates, monoterpenes contributed ~70% in the early morning at ~12 m above the forest canopy when isoprene emissions were low. In the afternoon, when vertical mixing and isoprene nitrate production were highest, the simulated contribution of isoprene-derived organic nitrates was greater than 90% at all altitudes, with the concentration of secondary isoprene nitrates increasing with altitude. Notably, reaction of isoprene with NO3 leading to isoprene nitrate formation was found to be significant (~8% of primary organic nitrate production) during the daytime, and monoterpene reactions with NO3 were simulated to comprise up to ~83% of primary organic nitrate production at night. Lastly, forest succession, wherein aspen trees are being replaced by pine and maple trees, was predicted to lead to increased afternoon concentrations of monoterpene-derived organic nitrates. This further underscores the need to understand the formation and fate of these species, which have different chemical pathways and oxidation products compared to isoprene-derived organic nitrates and can lead to secondary organic aerosol formation.

Details

Database :
OpenAIRE
Journal :
Atmospheric Chemistry and Physics, Atmospheric Chemistry and Physics, 2012, Atmospheric Chemistry and Physics, Vol 12, Iss 21, Pp 10125-10143 (2012)
Accession number :
edsair.doi.dedup.....bf94250dc74839b3faec991cc43dc0ac
Full Text :
https://doi.org/10.5194/acpd-12-17031-2012