Published May 2006 | Version Published
Journal Article Open

Global secondary organic aerosol from isoprene oxidation

Abstract

Inclusion of isoprene as a source of secondary organic aerosol (SOA) in a global model increases the global burden of SOA from all sources by more than a factor of two. The isoprene source substantially increases SOA concentrations in the free troposphere, because isoprene, and, more importantly, isoprene's oxidation products, have much greater concentrations at higher altitudes than other biogenic SOA precursors, highlighting the importance of semi-volatile organics for SOA formation. These results are robust with respect to increases in partitioning of non-isoprene oxidation products at higher altitudes and increased wet removal of isoprene oxidation products. This additional source of SOA enhances production of SOA from other parent hydrocarbons by 17%, and leads to an overall distribution of SOA that differs enough from previous predictions to warrant reevaluation of the radiative effects of organic carbon aerosol.

Additional Information

The work was supported by U.S. Environmental Protection Agency, grants RD-83107501-0 and R832158, and Department of Energy, grant DE-FG02-05ER63983. The authors thank Jesse Kroll and Daniel Jacob for useful discussions.

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Additional details

Identifiers

Eprint ID
7933
Resolver ID
CaltechAUTHORS:HENgrl06.367

Funding

Environmental Protection Agency (EPA)
RD-83107501-0
Environmental Protection Agency (EPA)
R832158
Department of Energy (DOE)
DE-FG02-05ER63983

Dates

Created
2023-02-15
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Updated
2023-02-15
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