Evolution of Biomass Burning Aerosols in the Near Field

 

Authors

Arthur J Sedlacek — Brookhaven National Laboratory
Larry Kleinman — Brookhaven National Laboratory
William Patrick Arnott — University of Nevada Reno
Kouji Adachi — Meteorological Research Institute
Peter R. Buseck — Arizona State University
Ernie R. Lewis — Brookhaven National Laboratory
Timothy B Onasch — Aerodyne Research
Michail Pikridas — Brookhaven National Laboratory
John E Shilling — Pacific Northwest National Laboratory
Stephen R. Springston — Brookhaven National Laboratory
Jian Wang — Washington University in St. Louis
Robert James Yokelson — University of Montana

Category

Aerosol Mixing State

Description

Biomass burning is a significant source of aerosols that can perturb Earth’s climate through the direct (both scattering and absorption), indirect (cloud formation and precipitation), and semi-direct (cloud dissipation) radiative effects. Despite much effort, quantities important to determining radiative forcing for these events still remain highly uncertain due to the inherent difficultly of conducting the required measurements and instrumentation limitations. Further adding to this uncertainty is that few field campaigns have been conducted in the northern temperate latitudes in spite of biomass burning producing about one-third of the PM2.5 in the US. During the summer and early fall of 2013, the Atmospheric Radiation Measurement (ARM) program of the U. S. Department of Energy (DOE) sponsored an aircraft-based field campaign to study the near-field evolution of particulate emissions from biomass burning. Key scientific objectives for the Biomass Burning Observation Project (BBOP) are to 1) quantify the downwind time evolution of microphysical, morphological, chemical, hygroscopic, and optical properties of aerosols generated by biomass burning, 2) use the time sequences of observations to constrain processes and parameterizations in a Lagrangian model of aerosol evolution, and 3) incorporate time evolution information into a single-column radiative transfer model for determining forcing per unit carbon burned. Discussion will be on the near-field evolution of aerosol mixing state and morphology, chemical composition, and microphysical processes that determine aerosol size distribution and single scattering albedo (SSA) of light absorbing aerosols. In cases studied, increases in the coating thickness of refractive black carbon (rBC) particles, organic aerosol/rBC ratio, scattering/CO ratio, and aerosol size distributions have been observed. Results are based on wildfires sampled in the US northwest and on controlled agricultural burns in the south-central Mississippi valley will be given.

Lead PI

Arthur J Sedlacek — Brookhaven National Laboratory