학술논문

Towards a satellite formaldehyde - in situ hybrid estimate for organic aerosol abundance
Document Type
Author abstract
Report
Source
Atmospheric Chemistry and Physics. March 4, 2019, Vol. 19 Issue 5, 2765
Subject
Volatile organic compounds -- Analysis -- Environmental aspects
Formaldehyde -- Analysis -- Environmental aspects -- Properties
Aerosols -- Environmental aspects -- Properties -- Distribution
Atmospheric chemistry -- Analysis
Oxidation-reduction reactions
Air quality
Remote sensing
Aldehydes
Pollution
Wildfires
Air pollution
Technology
Earth sciences
Company distribution practices
Analysis
Environmental aspects
Properties
Distribution
Language
English
ISSN
1680-7316
Abstract
Organic aerosol (OA) is one of the main components of the global particulate burden and intimately links natural and anthropogenic emissions with air quality and climate. It is challenging to accurately represent OA in global models. Direct quantification of global OA abundance is not possible with current remote sensing technology; however, it may be possible to exploit correlations of OA with remotely observable quantities to infer OA spatiotemporal distributions. In particular, formaldehyde (HCHO) and OA share common sources via both primary emissions and secondary production from oxidation of volatile organic compounds (VOCs). Here, we examine OA-HCHO correlations using data from summertime airborne campaigns investigating biogenic (NASA SEAC.sup.4 RS and DC3), biomass burning (NASA SEAC.sup.4 RS), and anthropogenic conditions (NOAA CalNex and NASA KORUS-AQ). In situ OA correlates well with HCHO (r=0.59-0.97), and the slope and intercept of this relationship depend on the chemical regime. For biogenic and anthropogenic regions, the OA-HCHO slopes are higher in low NO.sub.x conditions, because HCHO yields are lower and aerosol yields are likely higher. The OA-HCHO slope of wildfires is over 9 times higher than that for biogenic and anthropogenic sources. The OA-HCHO slope is higher for highly polluted anthropogenic sources (e.g., KORUS-AQ) than less polluted (e.g., CalNex) anthropogenic sources. Near-surface OAs over the continental US are estimated by combining the observed in situ relationships with HCHO column retrievals from NASA's Ozone Monitoring Instrument (OMI). HCHO vertical profiles used in OA estimates are from climatology a priori profiles in the OMI HCHO retrieval or output of specific period from a newer version of GEOS-Chem. Our OA estimates compare well with US EPA IMPROVE data obtained over summer months (e.g., slope =0.60-0.62, r=0.56 for August 2013), with correlation performance comparable to intensively validated GEOS-Chem (e.g., slope =0.57, r=0.56) with IMPROVE OA and superior to the satellite-derived total aerosol extinction (r=0.41) with IMPROVE OA. This indicates that OA estimates are not very sensitive to these HCHO vertical profiles and that a priori profiles from OMI HCHO retrieval have a similar performance to that of the newer model version in estimating OA. Improving the detection limit of satellite HCHO and expanding in situ airborne HCHO and OA coverage in future missions will improve the quality and spatiotemporal coverage of our OA estimates, potentially enabling constraints on global OA distribution.
Byline: Jin Liao, Thomas F. Hanisco, Glenn M. Wolfe, Jason St. Clair, Jose L. Jimenez, Pedro Campuzano-Jost, Benjamin A. Nault, Alan Fried, Eloise A. Marais, Gonzalo Gonzalez Abad, Kelly Chance, [...]