scholarly journals An improved model for estimating emissions of volatile organic compounds from forests in the eastern United States

1994 ◽  
Vol 99 (D6) ◽  
pp. 12773 ◽  
Author(s):  
Christopher D. Geron ◽  
Alex B. Guenther ◽  
Thomas E. Pierce
1999 ◽  
Vol 33 (23) ◽  
pp. 4176-4187 ◽  
Author(s):  
Paul J. Squillace ◽  
Michael J. Moran ◽  
Wayne W. Lapham ◽  
Curtis V. Price ◽  
Rick M. Clawges ◽  
...  

2021 ◽  
Vol 21 (8) ◽  
pp. 6331-6345
Author(s):  
Dianne Sanchez ◽  
Roger Seco ◽  
Dasa Gu ◽  
Alex Guenther ◽  
John Mak ◽  
...  

Abstract. We report OH reactivity observations by a chemical ionization mass spectrometer–comparative reactivity method (CIMS-CRM) instrument in a suburban forest of the Seoul metropolitan area (SMA) during the Korea–United States Air Quality Study (KORUS-AQ 2016) from mid-May to mid-June of 2016. A comprehensive observational suite was deployed to quantify reactive trace gases inside of the forest canopy including a high-resolution proton transfer reaction time-of-flight mass spectrometer (PTR-ToF-MS). An average OH reactivity of 30.7±5.1 s−1 was observed, while the OH reactivity calculated from CO, NO+NO2 (NOx), ozone (O3), sulfur dioxide (SO2), and 14 volatile organic compounds (VOCs) was 11.8±1.0 s−1. An analysis of 346 peaks from the PTR-ToF-MS accounted for an additional 6.0±2.2 s−1 of the total measured OH reactivity, leaving 42.0 % missing OH reactivity. A series of analyses indicate that the missing OH reactivity most likely comes from VOC oxidation products of both biogenic and anthropogenic origin.


2020 ◽  
Vol 239 ◽  
pp. 117783 ◽  
Author(s):  
Katherine B. Benedict ◽  
Anthony J. Prenni ◽  
Marwa M.H. El-Sayed ◽  
Arsineh Hecobian ◽  
Yong Zhou ◽  
...  

Author(s):  
Wayne W. Lapham ◽  
Janet M. Carter ◽  
John S. Zogorski ◽  
Joshua F. Valder

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