Impacts of the eruption of Miyakejima Volcano on air quality over far east Asia

• Published in: Journal of Geophysical Research: Atmospheres 2004-11, Vol.109 (D21), p.D21204.1-n/a
• Main Authors: Kajino, Mizuo, Ueda, Hiromasa, Satsumabayashi, Hikaru, An, Junling
• Format: Article
• Language: English
• Subjects: anthropogenic sulfate; Earth sciences; Earth, ocean, space; Exact sciences and technology; regional air pollution model; volcanic sulfate
• ISSN: 0148-0227; 2156-2202
• DOI: 10.1029/2004JD004762

A regional‐scale Eulerian Model System for Soluble Particles (MSSP) was constructed to simulate environmental changes caused by a SO42− increase as the result of the eruption of Miyakejima Volcano in the northwest Pacific Ocean. The measured volcanic SO2 emission was 9 Tg yr−1 for a year from the beginning of the eruption, July 2000. It is equivalent to 70% of global volcanic emission and 6.9% of global anthropogenic emission. Seasonal variations of the volcanic sulfate increase, and change of gas‐aerosol partitioning of NH3 and pH decrease of precipitation were studied using the MSSP model for 1 year from September 2000 to August 2001, together with observations performed at Happo Ridge observatory in the mountainous area in central Japan. In winter, northwesterly wind prevails, and volcanic SO42− was mainly transported southeastward to the Pacific Ocean while volcanic SO42− was transported southwestward to Japan, Korea, and Taiwan, owing to the subtropical high‐pressure system over the Pacific Ocean in summer. Temporal variations of SO42− concentrations and gas‐aerosol equilibrium of NH3 at Happo Ridge were well‐simulated. In the plume from the Asian continent, 98.7% of total SO42− was anthropogenic, and 63.5% of NH3 existed in aerosol phase as (NH4)2SO4. In the volcanic plume, 95.5% was volcanic, excessive sulfate fixed 100% of NH3 into aerosol phase, and aerosol was strongly acidified. Modeled annual mean pH of precipitation in Japan decreased by 0.3–1.0, which is equivalent to neutralization by yellow sand.