A numerical evaluation of global oceanic emissions of α-pinene and isoprene

• Published in: Atmospheric chemistry and physics Vol. 10; no. 4; pp. 2007 - 2015
• Main Authors: Luo, G., Yu, F.
• Format: Journal Article
• Language: English
• Published: Copernicus Publications 01.01.2010
• ISSN: 1680-7324; 1680-7316; 1680-7324
• DOI: 10.5194/acp-10-2007-2010

A numerical evaluation of global oceanic emissions of α-pinene and isoprene based on both "bottom-up" and "top-down" methods is presented. We infer that the global "bottom-up" oceanic emissions of α-pinene and isoprene are 0.013 TgC yr−1 and 0.32 TgC yr−1, respectively. By constraining global chemistry model simulations with the shipborne measurement of Organics over the Ocean Modifying Particles in both Hemispheres summer cruise, we derived the global "top-down" oceanic α-pinene source of 29.5 TgC yr−1 and isoprene source of 11.6 TgC yr−1. Both the "bottom-up" and "top-down" values are subject to large uncertainties. The incomplete understanding of the in-situ phytoplankton communities and their range of emission potentials significantly impact the estimated global "bottom-up" oceanic emissions, while the estimated total amounts of the global "top-down" oceanic sources can be influenced by emission parameterizations, model and input data spatial resolutions, boundary layer mixing processes, and the treatments of chemical reactions. The global oceanic α-pinene source and its impact on organic aerosol formation is significant based on "top-down" method, but is negligible based on "bottom-up" approach. Our research highlights the importance of carrying out further research (especially measurements) to resolve the large offset in the derived oceanic organic emission based on two different approaches.