Global distribution and climate forcing of marine organic aerosol – Part 2: Effects on cloud properties and radiative forcing

• Published in: Atmospheric Chemistry and Physics
• Main Authors: Gantt, B., Xu, J., Meskhidze, N., Zhang, Y., Nenes, A., Ghan, S. J., Liu, X., Easter, R., Zaveri, R.
• Format: Article in Journal/Newspaper
• Language: English
• Published: Copernicus Publications 2012
• Subjects: article; Verlagsveröffentlichung; Pacific; Southern Ocean; North Atlantic
• Online Access: https://doi.org/10.5194/acp-12-6555-2012; https://noa.gwlb.de/receive/cop_mods_00045948; https://noa.gwlb.de/servlets/MCRFileNodeServlet/cop_derivate_00045568/acp-12-6555-2012.pdf; https://acp.copernicus.org/articles/12/6555/2012/acp-12-6555-2012.pdf

A series of simulations with the Community Atmosphere Model version 5 (CAM5) with a 7-mode Modal Aerosol Model were conducted to assess the changes in cloud microphysical properties and radiative forcing resulting from marine organic aerosols. Model simulations show that the anthropogenic aerosol indirect forcing (AIF) predicted by CAM5 is decreased in absolute magnitude by up to 0.09 W m−2 (7%) when marine organic aerosols are included. Changes in the AIF from marine organic aerosols are associated with small global increases in low-level in-cloud droplet number concentration and liquid water path of 1.3 cm−3 (1.5%) and 0.22 g m−2 (0.5%), respectively. Areas especially sensitive to changes in cloud properties due to marine organic aerosol include the Southern Ocean, North Pacific Ocean, and North Atlantic Ocean, all of which are characterized by high marine organic emission rates. As climate models are particularly sensitive to the background aerosol concentration, this small but non-negligible change in the AIF due to marine organic aerosols provides a notable link for ocean-ecosystem marine low-level cloud interactions and may be a candidate for consideration in future earth system models.