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Title: Diel cycle impacts on the chemical and light absorption properties of organic carbon aerosol from wildfires in the western United States

Abstract

Organic aerosol (OA) emissions from biomass burning have been the subject of intense research in recent years, involving a combination of field campaigns and laboratory studies. These efforts have aimed at improving our limited understanding of the diverse processes and pathways involved in the atmospheric processing and evolution of OA properties, culminating in their accurate parameterizations in climate and chemical transport models. To bring closure between laboratory and field studies, wildfire plumes in the western United States were sampled and characterized for their chemical and optical properties during the ground-based segment of the 2019 Fire Influence on Regional to Global Environments and Air Quality (FIREX-AQ) field campaign. Using a custom-developed multiwavelength integrated photoacoustic-nephelometer spectrometer in conjunction with a suite of instruments, including an oxidation flow reactor equipped to generate hydroxyl (OH•) or nitrate (NO3•) radicals to mimic daytime or nighttime oxidative aging processes, we investigated the effects of multiple equivalent hours of OH• or NO3• exposure on the chemical composition and mass absorption cross-sections (MAC(λ)) at 488 and 561 nm of OA emitted from wildfires in Arizona and Oregon. We found that OH• exposure induced a slight initial increase in absorption corresponding to short timescales; however, at longer timescales, themore » wavelength-dependent MAC(λ) decreased by a factor of 0.72 ± 0.08, consistent with previous laboratory studies and reports of photobleaching. On the other hand, NO3• exposure increased MAC(λ) by a factor of up to 1.69 ± 0.38. We also noted some sensitivity of aerosol aging to different fire conditions between Arizona and Oregon. The MAC(λ) enhancement following NO3• exposure was found to correlate with an enhancement in CHO1N and CHOgt1N ion families measured by an Aerodyne aerosol mass spectrometer.« less

Authors:
ORCiD logo; ; ; ; ORCiD logo; ; ; ORCiD logo;
Publication Date:
Research Org.:
Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Atmospheric Radiation Measurement (ARM) Data Center
Sponsoring Org.:
USDOE Office of Science (SC), Biological and Environmental Research (BER); National Aeronautics and Space Administration (NASA); National Science Foundation (NSF)
OSTI Identifier:
1812411
Alternate Identifier(s):
OSTI ID: 1814455
Grant/Contract Number:  
SC0021011; 80NSSC18K1414; NNH20ZDA001N-ACCDAM; AGS-1455215; AGS-1926817
Resource Type:
Published Article
Journal Name:
Atmospheric Chemistry and Physics (Online)
Additional Journal Information:
Journal Name: Atmospheric Chemistry and Physics (Online) Journal Volume: 21 Journal Issue: 15; Journal ID: ISSN 1680-7324
Publisher:
Copernicus GmbH
Country of Publication:
Germany
Language:
English
Subject:
54 ENVIRONMENTAL SCIENCES

Citation Formats

Sumlin, Benjamin, Fortner, Edward, Lambe, Andrew, Shetty, Nishit J., Daube, Conner, Liu, Pai, Majluf, Francesca, Herndon, Scott, and Chakrabarty, Rajan K. Diel cycle impacts on the chemical and light absorption properties of organic carbon aerosol from wildfires in the western United States. Germany: N. p., 2021. Web. doi:10.5194/acp-21-11843-2021.
Sumlin, Benjamin, Fortner, Edward, Lambe, Andrew, Shetty, Nishit J., Daube, Conner, Liu, Pai, Majluf, Francesca, Herndon, Scott, & Chakrabarty, Rajan K. Diel cycle impacts on the chemical and light absorption properties of organic carbon aerosol from wildfires in the western United States. Germany. https://doi.org/10.5194/acp-21-11843-2021
Sumlin, Benjamin, Fortner, Edward, Lambe, Andrew, Shetty, Nishit J., Daube, Conner, Liu, Pai, Majluf, Francesca, Herndon, Scott, and Chakrabarty, Rajan K. Mon . "Diel cycle impacts on the chemical and light absorption properties of organic carbon aerosol from wildfires in the western United States". Germany. https://doi.org/10.5194/acp-21-11843-2021.
@article{osti_1812411,
title = {Diel cycle impacts on the chemical and light absorption properties of organic carbon aerosol from wildfires in the western United States},
author = {Sumlin, Benjamin and Fortner, Edward and Lambe, Andrew and Shetty, Nishit J. and Daube, Conner and Liu, Pai and Majluf, Francesca and Herndon, Scott and Chakrabarty, Rajan K.},
abstractNote = {Organic aerosol (OA) emissions from biomass burning have been the subject of intense research in recent years, involving a combination of field campaigns and laboratory studies. These efforts have aimed at improving our limited understanding of the diverse processes and pathways involved in the atmospheric processing and evolution of OA properties, culminating in their accurate parameterizations in climate and chemical transport models. To bring closure between laboratory and field studies, wildfire plumes in the western United States were sampled and characterized for their chemical and optical properties during the ground-based segment of the 2019 Fire Influence on Regional to Global Environments and Air Quality (FIREX-AQ) field campaign. Using a custom-developed multiwavelength integrated photoacoustic-nephelometer spectrometer in conjunction with a suite of instruments, including an oxidation flow reactor equipped to generate hydroxyl (OH•) or nitrate (NO3•) radicals to mimic daytime or nighttime oxidative aging processes, we investigated the effects of multiple equivalent hours of OH• or NO3• exposure on the chemical composition and mass absorption cross-sections (MAC(λ)) at 488 and 561 nm of OA emitted from wildfires in Arizona and Oregon. We found that OH• exposure induced a slight initial increase in absorption corresponding to short timescales; however, at longer timescales, the wavelength-dependent MAC(λ) decreased by a factor of 0.72 ± 0.08, consistent with previous laboratory studies and reports of photobleaching. On the other hand, NO3• exposure increased MAC(λ) by a factor of up to 1.69 ± 0.38. We also noted some sensitivity of aerosol aging to different fire conditions between Arizona and Oregon. The MAC(λ) enhancement following NO3• exposure was found to correlate with an enhancement in CHO1N and CHOgt1N ion families measured by an Aerodyne aerosol mass spectrometer.},
doi = {10.5194/acp-21-11843-2021},
journal = {Atmospheric Chemistry and Physics (Online)},
number = 15,
volume = 21,
place = {Germany},
year = {Mon Aug 09 00:00:00 EDT 2021},
month = {Mon Aug 09 00:00:00 EDT 2021}
}

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