TY - JOUR
T1 - Contribution of feldspar and marine organic aerosols to global ice nucleating particle concentrations
AU - Vergara-Temprado, Jesús
AU - Murray, Benjamin J.
AU - Wilson, Theodore W.
AU - O'Sullivan, Daniel
AU - Browse, Jo
AU - Pringle, Kirsty J.
AU - Ardon-Dryer, Karin
AU - Bertram, Allan K.
AU - Burrows, Susannah M.
AU - Ceburnis, Darius
AU - Demott, Paul J.
AU - Mason, Ryan H.
AU - O'Dowd, Colin D.
AU - Rinaldi, Matteo
AU - Carslaw, Ken S.
N1 - Funding Information:
This study has been funded by the European Union' Seventh Framework Programme (FP7/2007-797 2013) under grant agreement no. 603445 (BACCHUS), the European Research Council (ERC, 240449 ICE and 648661 MarineIce) and the National Environmental Research Council, (NERC, NE/I013466/1; NE/K004417/1). The global model simulations were performed on the ARCHER UK National Supercomputing Service. We acknowledge Franz Conen and Christoph Huglin who contributed data used in this paper. Ken S. Carslaw is a Royal Society Wolfson Merit Award holder. Paul DeMott acknowledges support from the US National Science Foundation grant AGS1358495. Susannah Burrows was supported as part of the Accelerated Climate Modeling for Energy (ACME) project, funded by the US Department of Energy, Office of Science, Office of Biological and Environmental Research.
Publisher Copyright:
© Author(s) 2017.
PY - 2017/3/15
Y1 - 2017/3/15
N2 - Ice-nucleating particles (INPs) are known to affect the amount of ice in mixed-phase clouds, thereby influencing many of their properties. The atmospheric INP concentration changes by orders of magnitude from terrestrial to marine environments, which typically contain much lower concentrations. Many modelling studies use parameterizations for heterogeneous ice nucleation and cloud ice processes that do not account for this difference because they were developed based on INP measurements made predominantly in terrestrial environments without considering the aerosol composition. Errors in the assumed INP concentration will influence the simulated amount of ice in mixed-phase clouds, leading to errors in top-of-atmosphere radiative flux and ultimately the climate sensitivity of the model. Here we develop a global model of INP concentrations relevant for mixed-phase clouds based on laboratory and field measurements of ice nucleation by K-feldspar (an ice-active component of desert dust) and marine organic aerosols (from sea spray). The simulated global distribution of INP concentrations based on these two species agrees much better with currently available ambient measurements than when INP concentrations are assumed to depend only on temperature or particle size. Underestimation of INP concentrations in some terrestrial locations may be due to the neglect of INPs from other terrestrial sources. Our model indicates that, on a monthly average basis, desert dusts dominate the contribution to the INP population over much of the world, but marine organics become increasingly important over remote oceans and they dominate over the Southern Ocean. However, day-to-day variability is important. Because desert dust aerosol tends to be sporadic, marine organic aerosols dominate the INP population on many days per month over much of the mid- and high-latitude Northern Hemisphere. This study advances our understanding of which aerosol species need to be included in order to adequately describe the global and regional distribution of INPs in models, which will guide ice nucleation researchers on where to focus future laboratory and field work.
AB - Ice-nucleating particles (INPs) are known to affect the amount of ice in mixed-phase clouds, thereby influencing many of their properties. The atmospheric INP concentration changes by orders of magnitude from terrestrial to marine environments, which typically contain much lower concentrations. Many modelling studies use parameterizations for heterogeneous ice nucleation and cloud ice processes that do not account for this difference because they were developed based on INP measurements made predominantly in terrestrial environments without considering the aerosol composition. Errors in the assumed INP concentration will influence the simulated amount of ice in mixed-phase clouds, leading to errors in top-of-atmosphere radiative flux and ultimately the climate sensitivity of the model. Here we develop a global model of INP concentrations relevant for mixed-phase clouds based on laboratory and field measurements of ice nucleation by K-feldspar (an ice-active component of desert dust) and marine organic aerosols (from sea spray). The simulated global distribution of INP concentrations based on these two species agrees much better with currently available ambient measurements than when INP concentrations are assumed to depend only on temperature or particle size. Underestimation of INP concentrations in some terrestrial locations may be due to the neglect of INPs from other terrestrial sources. Our model indicates that, on a monthly average basis, desert dusts dominate the contribution to the INP population over much of the world, but marine organics become increasingly important over remote oceans and they dominate over the Southern Ocean. However, day-to-day variability is important. Because desert dust aerosol tends to be sporadic, marine organic aerosols dominate the INP population on many days per month over much of the mid- and high-latitude Northern Hemisphere. This study advances our understanding of which aerosol species need to be included in order to adequately describe the global and regional distribution of INPs in models, which will guide ice nucleation researchers on where to focus future laboratory and field work.
UR - http://www.scopus.com/inward/record.url?scp=85015640914&partnerID=8YFLogxK
U2 - 10.5194/acp-17-3637-2017
DO - 10.5194/acp-17-3637-2017
M3 - Article
AN - SCOPUS:85015640914
SN - 1680-7316
VL - 17
SP - 3637
EP - 3658
JO - Atmospheric Chemistry and Physics
JF - Atmospheric Chemistry and Physics
IS - 5
ER -