Field Survey of Trans-boundary Air Pollution with High Time Resolution at Coastal Sites on the Sea of Japan during Winter in Japan}

An intensive field survey, with 6-h measurement intervals, of concentrations of chemical species in particulate matter and gaseous compounds was carried out at coastal sites on the Sea of Japan during winter. The concentration variation of SO₂(g) and HNO₃(g) were well correlated, whereas the NH₃(g) concentration variation had no correlation with those of SO₂(g) and HNO₃(g). The NH₄ ⁺ (p)/non-sea-salt- (nss-)SO₄ ^{2 −}(p) ratio in particulate matter was mainly affected by the location of the sampling site. One or more concentration peaks of nss-Ca^{2 +} for survey period were observed. Backward trajectories analyses for the highest nss-Ca^{2 +} concentration peaks showed some inconsistency in pathways. We consider that insufficient mixing of the atmosphere and/or insufficient time for the transported air pollutants to react with those discharged locally are the most likely explanations for the discrepancies between the measured products [HNO₃][NH₃] and the calculated values.     

Significant geographic gradients in particulate sulfate over Japan determined from multiple-site measurements and a chemical transport model: Impacts of transboundary pollution from the Asian continent

We found a significant geographic gradient (longitudinal and latitudinal) in the sulfate (SO₄^2?) concentrations measured at multiple sites over the East Asian Pacific Rim region. Furthermore, the observed gradient was well reproduced by a regional chemical transport model. The observed and modeled SO₄^2? concentrations were higher at the sites closer to the Asian continent. The concentrations of SO₄^2? from China as calculated by the model also showed the fundamental features of the longitudinal/latitudinal gradient. The proportional contribution of Chinese SO₄^2? to the total in Japan throughout the year was above 50–70% in the control case, using data for Chinese sulfur dioxide (SO₂) emission from the Regional Emission Inventory in Asia (40–60% in the low Chinese emissions case, using Chinese SO₂ emissions data from the State Environmental Protection Administration of China), with a winter maximum of approximately 65–80%, although the actual concentrations of SO₄^2? from China were highest in summer. The multiple-site measurements and the model analysis strongly suggest that the SO₄^2? concentrations in Japan were influenced by the outflow from the Asian continent, and this influence was greatest in the areas closer to the Asian continent. In contrast, we found no longitudinal/latitudinal gradient in SO₂ concentrations; instead SO₂ concentrations were significantly correlated with local SO₂ emissions. Our results show that large amounts of particulate sulfate are transported over long distances from the East Asian Pacific Rim region, and consequently the SO₄^2? concentrations in Japan are controlled by the transboundary outflow from the Asian continent.     

Estimation of the amount of dry deposition in an urban area (Kobe city, Japan) by the inferential method

The amount of dry deposition of SO₂(g) and HNO₃(g) in an urban area in Japan has been estimated by the inferential method. The mean annual dry deposition of SO₂(g) (2.91 kgS/ha/year) was close to or less than that in the Clean Air Status and Trends Network (CASTNet) of the U.S. (3.59 kgS/ha/year). The mean annual dry deposition of HNO₃(g) (10.8 kgN/ha/year) was approximately six times larger than that in CASTNet (1.85 kgN/ha/year). The proportions of dry/(dry+wet) deposition for sulfur and nitrogen were 0.301 and 0.785, respectively.