ALBERT

Description: Long-range transport of Asian dust and air pollutants are major environmental concerns of Taiwan during the winter monsoon season when northeasterly winds prevail following passages of cold fronts. Based on hourly measurements of Taiwan Environmental Protection Administration (TEPA) air quality monitoring stations, Lidar and in-situ IC, a significant long-range transport dust and air pollutants event on 18 March 2005 has been identified. During this episode, drastically elevated concentrations of PM10, CO and SO2 along with the strong northeasterly on 18 March were observed over background Wanli station, with peaks of about 170 μgm−3, 1.0 PPM and 14 ppb, respectively. We have found that air masses of air pollutants and Asian dust are transported separately. The major component of the first PM10 peak were air pollutants, evidenced by the consistent peaks of SO42− and NO3− measured by in-situ IC, while no significant depolarization was measured by Lidar. In contrast, the evident non-spherical particles and hourly PM10 concentration consistently varied with Ca2+ indicating that mineral dust was the major component of the second peak. Numerical results showed significant agreement of temporal and vertical variation of aerosol concentration with observations. The phenomena of split air parcels between air pollutants and Asian dust transported to Taiwan are strongly associated with the transport paths and stable and dry atmospheric boundary conditions.

Description: The aim of this study is to investigate the seasonal variations in the physicochemical properties of atmospheric ultra-fine particles (UFPs, d ≤ 100 nm) and submicron particles (PM1, d ≤ 1 µm) in an east Asian urban area, which are hypothesized to be affected by the interchange of summer and winter monsoons. An observation experiment was conducted at TARO (Taipei Aerosol and Radiation Observatory), an urban aerosol station in Taipei, Taiwan, from October 2012 to August 2013. The measurements included the mass concentration and chemical composition of UFPs and PM1, as well as the particle number concentration (PNC) and the particle number size distribution (PSD) with size range of 4–736 nm. The results indicated that the mass concentration of PM1 was elevated during cold seasons with a peak level of 18.5 µg m−3 in spring, whereas the highest concentration of UFPs was measured in summertime with a mean of 1.64 µg m−3. Moreover, chemical analysis revealed that the UFPs and PM1 were characterized by distinct composition; UFPs were composed mostly of organics, whereas ammonium and sulfate were the major constituents of PM1. The seasonal median of total PNCs ranged from 13.9  ×  103 cm−3 in autumn to 19.4  ×  103 cm−3 in spring. Median concentrations for respective size distribution modes peaked in different seasons. The nucleation-mode PNC (N4 − 25) peaked at 11.6  ×  103 cm−3 in winter, whereas the Aitken-mode (N25 − 100) and accumulation-mode (N100 − 736) PNC exhibited summer maxima at 6.0  ×  103 and 3.1  ×  103 cm−3, respectively. The change in PSD during summertime was attributed to the enhancement in the photochemical production of condensable organic matter that, in turn, contributed to the growth of aerosol particles in the atmosphere. In addition, clear photochemical production of particles was observed, mostly in the summer season, which was characterized by average particle growth and formation rates of 4.0 ± 1.1 nm h−1 and 1.4 ± 0.8 cm−3 s−1, respectively. The prevalence of new particle formation (NPF) in summer was suggested as a result of seasonally enhanced photochemical oxidation of SO2 that contributed to the production of H2SO4, and a low level of PM10 (d ≤ 10 µm) that served as the condensation sink. Regarding the sources of aerosol particles, correlation analysis of the PNCs against NOx revealed that the local vehicular exhaust was the dominant contributor of the UFPs throughout the year. Conversely, the Asian pollution outbreaks had significant influence in the PNC of accumulation-mode particles during the seasons of winter monsoons. The results of this study implied the significance of secondary organic aerosols in the seasonal variations of UFPs and the influences of continental pollution outbreaks in the downwind areas of Asian outflows.

Description: As a part of the CAREBeijing-2008 campaign, observations of O3, oxides of nitrogen (NOx and NOy), CO, and hydrocarbons (NMHCs) were carried out at the air quality observatory of the Peking University in Beijing, China during August 2008, including the period of the 29th Summer Olympic Games. The measurements were compared to those of the CAREBeijing-2006 campaign to evaluate the effectiveness of the air pollution control measures, which were conducted for improving the air quality in Beijing during the Olympics. The results indicate that significant reduction in the emissions of primary air pollutants had been achieved; the monthly averages of NOx, NOy, CO, and NMHCs reduced by 42.2, 56.5, 27.8, and 49.7 %, respectively. In contrast to the primary pollutants, the averaged mixing ratio of O3 increased by 42.2 %. Nevertheless, it was revealed that the ambient levels of total oxidants (Ox=O3+NO2+1.5NOz) and NOz reduced by 21.3 and 77.4 %, respectively. The contradictions between O3 and Ox were further examined in two case studies. Ozone production rates of 30–70 ppbv hr−1 and OPEx of ~8 mole mole−1 were observed on a clear-sky day in spite of the reduced levels of precursors. In that case, it was found that the concentrations of O3 increased with the increasing NO2/NO ratio, whereas the NOz concentrations leveled off when NO2/NO〉8. Consequently, the ratio of O3 to NOz increased to above 10, indicating the shift from VOC-sensitive regime to NOx-sensitive regime. However, in the other case, it was found that the O3 production was inhibited significantly due to substantial reduction in the ambient levels of NMHCs. According to the observations, it was suggested that the O3/Ox production rates in Beijing should have been reduced for the reduction in the emissions of precursors during the Olympic period; however, the nighttime O3 levels were increased for decline in the NO-O3 titration, and the midday O3 peak levels were elevated for the shift in the photochemical regime and the inhibition of NOz formation.

Description: Long-range transport of Asian dust and air pollutants are major environmental concerns of Taiwan during the winter monsoon season when northeasterly winds prevail following passages of cold fronts. Based on hourly measurements of Taiwan Environmental Protection Administration (TEPA) air quality monitoring stations, Lidar and in-situ IC, a significant long-range transport dust and air pollutants event on 18 March 2005 has been identified. During this episode, drastically elevated concentrations of PM10, CO and SO2 along with the strong northeasterly on 18 March were observed over background Wanli station, with peaks of about 170 μgm−3, 1.0 ppm and 14 ppb, respectively. We have found that air masses of air pollutants and Asian dust are transported separately. Although the mixing takes place on the way to Taiwan, it mixes slightly when they arrived in Taiwan. The major component of the first PM10 peak were air pollutants, evidenced by the consistent peaks of SO42− and NO3