Japan Geoscience Union Meeting 2018

Presentation information

[JJ] Oral

A (Atmospheric and Hydrospheric Sciences) » A-AS Atmospheric Sciences, Meteorology & Atmospheric Environment

[A-AS07] Stratosphere-troposphere Processes And their Role in Climate

Wed. May 23, 2018 10:45 AM - 12:15 PM A07 (Tokyo Bay Makuhari Hall)

convener:Shingo Watanabe(Japan Agency for Marine-Earth Science and Technology), Yoshio Kawatani(Japan Agency for Marine-Earth Science and Technology), Takashi Sekiya(国立研究開発法人 海洋研究開発機構, 共同), Kaoru Sato(Department of Earth and Planetary Science, Graduate School of Science, The University of Tokyo), Chairperson:Sekiya Takashi

11:00 AM - 11:15 AM

[AAS07-08] Pre-Industrial Carbonyl Sulphide studied by 1-D photochemical model, future implications

★Invited Papers

*Sebastian Danielache1,2, Masumi Shinkai1 (1.Department of Materials & Life Sciences, Faculty of Science & Technology, Sophia University, 2.Earth-Life Science Institute )

Keywords:SSA, Pre-Industrial

Carbonyl sulfide (OCS) has a large lifetime for tropospheric consitions making it the most abundant reduced sulfur compound in the atmosphere. Stratospheric oxidation of OCS produces a sulfate aerosol layer between 17 and 30 km. This stratosppheric sulfur aerosol (SSA) also known as the Junge Layer affects the planet's Albedo and catalysis the hydrolysis of N2O5, promiting mid-latitude ozone deplition. While volcanic eruptions are an important source of stratospheric sulfate they are sporadic. Recent studies have extended the isotopic database and hte kinetic data related to this compound. Ice core studies show that pre-industrial tropospheric levels of OCS were 372 ppt while current levels are 500 ppt. In this study, we create a 1-D photochemical model that includes stable isotopes has an additional tool for model calibrations and consider the historical variation of anthropogenic emissions of OCS and its tropospheric precursor CS2.

In orer to calculate the OCS atmospheric vertical profile, we developed a one-dimensional photochemical model that takes into account chemistry, transport, deposition, stable isotopes, and high-resultion UV absorption spectrum. This last feature is important since the main isotopic imprint if the stratospheric oxidation pathway of produced by photo-dissociation. The combinationod the updated kinetic isotopic data with different emission scenarios presents a new hypotheis that challenges the current understanting of the stratospheric sulfur aerosol. Our fidings show that 34% of today's SSA is anthropogenic. Furthemore, the anthrpogenic contribution to SSA means that an estimate of -0.16 Wm2 of radiative forcing should be accounted in pre-industrial pollution-free models.