TY - JOUR
T1 - Comparison between Spatially Resolved Airborne Flux Measurements and Emission Inventories of Volatile Organic Compounds in Los Angeles
AU - Pfannerstill, Eva Y.
AU - Arata, Caleb
AU - Zhu, Qindan
AU - Schulze, Benjamin C.
AU - Woods, Roy
AU - Harkins, Colin
AU - Schwantes, Rebecca H.
AU - McDonald, Brian C.
AU - Seinfeld, John H.
AU - Bucholtz, Anthony
AU - Cohen, Ronald C.
AU - Goldstein, Allen H.
N1 - Publisher Copyright:
© 2023 The Authors. Published by American Chemical Society
PY - 2023/10/17
Y1 - 2023/10/17
N2 - Los Angeles is a major hotspot for ozone and particulate matter air pollution in the United States. Ozone and PM2.5 in this region have not improved substantially for the past decade, despite a reduction in vehicular emissions of their precursors, NOx and volatile organic compounds (VOCs). This reduction in “traditional” sources has made the current emission mixture of air pollutant precursors more uncertain. To map and quantify emissions of a wide range of VOCs in this urban area, we performed airborne eddy covariance measurements with wavelet analysis. VOC fluxes measured include tracers for source categories, such as traffic, vegetation, and volatile chemical products (VCPs). Mass fluxes were dominated by oxygenated VOCs, with ethanol contributing ∼29% of the total. In terms of OH reactivity and aerosol formation potential, terpenoids contributed more than half. Observed fluxes were compared with two commonly used emission inventories: the California Air Resources Board inventory and the combination of the Biogenic Emission Inventory System with the Fuel-based Inventory of Vehicle Emissions combined with Volatile Chemical Products (FIVE-VCP). The comparison shows mismatches regarding the amount, spatial distribution, and weekend effects of observed VOC emissions with the inventories. The agreement was best for typical transportation related VOCs, while discrepancies were larger for biogenic and VCP-related VOCs.
AB - Los Angeles is a major hotspot for ozone and particulate matter air pollution in the United States. Ozone and PM2.5 in this region have not improved substantially for the past decade, despite a reduction in vehicular emissions of their precursors, NOx and volatile organic compounds (VOCs). This reduction in “traditional” sources has made the current emission mixture of air pollutant precursors more uncertain. To map and quantify emissions of a wide range of VOCs in this urban area, we performed airborne eddy covariance measurements with wavelet analysis. VOC fluxes measured include tracers for source categories, such as traffic, vegetation, and volatile chemical products (VCPs). Mass fluxes were dominated by oxygenated VOCs, with ethanol contributing ∼29% of the total. In terms of OH reactivity and aerosol formation potential, terpenoids contributed more than half. Observed fluxes were compared with two commonly used emission inventories: the California Air Resources Board inventory and the combination of the Biogenic Emission Inventory System with the Fuel-based Inventory of Vehicle Emissions combined with Volatile Chemical Products (FIVE-VCP). The comparison shows mismatches regarding the amount, spatial distribution, and weekend effects of observed VOC emissions with the inventories. The agreement was best for typical transportation related VOCs, while discrepancies were larger for biogenic and VCP-related VOCs.
KW - California
KW - air quality
KW - airborne
KW - emissions
KW - fluxes
KW - inventory
KW - volatile organic compounds
UR - https://www.scopus.com/pages/publications/85174642460
U2 - 10.1021/acs.est.3c03162
DO - 10.1021/acs.est.3c03162
M3 - Article
C2 - 37791848
AN - SCOPUS:85174642460
SN - 0013-936X
VL - 57
SP - 15533
EP - 15545
JO - Environmental Science and Technology
JF - Environmental Science and Technology
IS - 41
ER -