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Radiative and chemical implications of the size and composition of aerosol particles in the existing or modified global stratosphere

  • Daniel M. Murphy (Corresponding author)
  • , Karl D. Froyd
  • , Ilann Bourgeois
  • , Charles A. Brock
  • , Agnieszka Kupc
  • , Jeff Peischl
  • , Gregory P. Schill
  • , Chelsea R. Thompson
  • , Christina J. Williamson
  • , Pengfei Yu

Publications: Contribution to journalArticlePeer Reviewed

Abstract

The size of aerosol particles has fundamental effects on their chemistry and radiative effects. We explore those effects using aerosol size and composition data in the lowermost stratosphere along with calculations of light scattering. In the size range between about 0.1 and 1.0ĝ€μm diameter (accumulation mode), there are at least two modes of particles in the lowermost stratosphere. The larger mode consists mostly of particles produced in the stratosphere, and the smaller mode consists mostly of particles transported from the troposphere. The stratospheric mode is similar in the Northern and Southern Hemisphere, whereas the tropospheric mode is much more abundant in the Northern Hemisphere. The purity of sulfuric acid particles in the stratospheric mode shows that there is limited production of secondary organic aerosol in the stratosphere, especially in the Southern Hemisphere. Out of eight sets of flights sampling the lowermost stratosphere (four seasons and two hemispheres) there were three with large injections of specific materials: volcanic, biomass burning, or dust. The stratospheric and tropospheric modes have very different roles for radiative effects on climate and for heterogeneous chemistry. Because the larger particles are more efficient at scattering light, most of the radiative effect in the lowermost stratosphere is due to stratospheric particles. In contrast, the tropospheric particles can have more surface area, at least in the Northern Hemisphere. The surface area of tropospheric particles could have significant implications for heterogeneous chemistry because these particles, which are partially neutralized and contain organics, do not correspond to the substances used for laboratory studies of stratospheric heterogeneous chemistry. We then extend the analysis of size-dependent properties to particles injected into the stratosphere, either intentionally or from volcanoes. There is no single size that will simultaneously maximize the climate impact relative to the injected mass, infrared heating, potential for heterogeneous chemistry, and undesired changes in direct sunlight. In addition, light absorption in the far ultraviolet is identified as an issue requiring more study for both the existing and potentially modified stratosphere.

Original languageEnglish
Pages (from-to)8915–8932
Number of pages18
JournalAtmospheric Chemistry and Physics
Volume21
Issue number11
DOIs
Publication statusPublished - 11 Jun 2021

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 12 - Responsible Consumption and Production
    SDG 12 Responsible Consumption and Production
  2. SDG 13 - Climate Action
    SDG 13 Climate Action

Austrian Fields of Science 2012

  • 105904 Environmental research
  • 103039 Aerosol physics

Keywords

  • DISTRIBUTIONS
  • IMPACT
  • IN-SITU MEASUREMENTS
  • LIFE-CYCLE
  • METEORIC MATERIAL
  • MICROPHYSICAL SIMULATIONS
  • MODEL
  • OZONE DEPLETION
  • SULFATE
  • UPPER TROPOSPHERE

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