Articles | Volume 19, issue 6
https://doi.org/10.5194/acp-19-3905-2019
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-19-3905-2019
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
In situ measurements of trace gases, PM, and aerosol optical properties during the 2017 NW US wildfire smoke event
Vanessa Selimovic
Department of Chemistry, University of Montana, Missoula, MT 59812, USA
Robert J. Yokelson
CORRESPONDING AUTHOR
Department of Chemistry, University of Montana, Missoula, MT 59812, USA
Gavin R. McMeeking
Handix Scientific LLC, 5485 Conestoga Court, Suite 104B, Boulder, CO 80301, USA
Sarah Coefield
Missoula City-County Health Department, Missoula, MT 59801, USA
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- Emissions of Trace Organic Gases From Western U.S. Wildfires Based on WE‐CAN Aircraft Measurements W. Permar et al. 10.1029/2020JD033838
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Discussed (final revised paper)
Latest update: 14 Dec 2024
Short summary
A massive wildfire smoke episode impacted the western US and Canada in summer 2017. We measured CO, other trace gases, PM, BC, and aerosol optical properties at a heavily impacted, ground-based site affected by this event. Brown carbon diminished as smoke aged but was a persistent component of the regional smoke, accounting for about half of aerosol absorption at 401 nm on average. The PM / CO ratios suggested aerosol evaporation was dominant at the surface at smoke ages of up to ~ 1–2 days.
A massive wildfire smoke episode impacted the western US and Canada in summer 2017. We measured...
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Final-revised paper
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