ALBERT

Description: In order to study the temporal and spatial variations of PM2.5 and its chemical compositions in the region of Beijing, Tianjin, and Hebei (BTH), PM2.5 samples were collected at four urban sites in Beijing (BJ), Tianjin (TJ), Shijiazhuang (SJZ), and Chengde (CD), and also one site at Shangdianzi (SDZ) regional background station over four seasons from 2009 to 2010. The samples were weighted for mass concentrations and analyzed in the laboratory for chemical profiles of 19 elements (Al, As, Ba, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Ni, P, Pb, Sr, Ti, V, and Zn), eight water-soluble inorganic ions (Na+, NH4+, K+, Mg2+, Ca2+, Cl−, NO3−, and SO42−, and carbon fractions (OC and EC). The concentrations of PM2.5 and its major chemical species were season dependent and showed spatially similar characteristics in the plain area of BTH. The average annual concentrations of PM2.5 were 71.8–191.2 μg m−3 at the five sites, with more than 90% of sampling days exceeding 50 μg m−3 at BJ, TJ, and SJZ. PM2.5 pollution was most serious at SJZ, and the annual concentrations of PM2.5, secondary inorganic ions, OC, EC, and most crustal elements were all highest. Due to stronger photochemical oxidation, the sum of concentrations of secondary inorganic ions (NH4+, NO3−, and SO42− was highest in the summer at SDZ, BJ, TJ, and CD. Analysis of electric charges of water-soluble inorganic ions indicated the existence of nitric acid or hydrochloric acid in PM2.5. For all five sites, the concentrations of OC, EC and also secondary organic carbon (SOC) in the spring and summer were lower than those in the autumn and winter. SOC had more percentages of increase than primary organic carbon (POC) during the winter. The sums of crustal elements (Al, Ca, Fe, Mg, Ti, Ba, and Sr) were higher in the spring and autumn owing to more days with blowing or floating dust. The concentrations of heavy metals were at higher levels in the BTH area by comparison with other studies. In Shijiazhuang and Chengde, the PM2.5 pollution was dominated by coal combustion. Motor vehicle exhausts and coal combustion emissions both played important roles in Tianjin PM2.5 pollution. However, motor vehicle exhausts had played a more important role in Beijing owing to the reduction of coal consumption and sharp increase of cars in recent years. At SDZ, regional transportation of air pollutants from southern urban areas was significant.

Description: This study investigates the effects of the total solar eclipse of 22 July 2009 on surface ozone and other photo-oxidants over China. A box model was used to study the sensitivity of ozone to the limb darkening effect during an eclipse event, and to show that the impact on ozone is small (less than 0.5 %). In addition, the regional model WRF-Chem was applied to study the effects of the eclipse on meteorological and chemical parameters, focusing on different regions in China. Chemical and meteorological observations were used to validate the model and to show that it can capture the effects of the total solar eclipse well. Model calculations show distinct differences in the spatial distributions of meteorological and chemical parameters with and without the eclipse. The maximum impacts of the eclipse occur over the area of totality, where there is a decrease in surface temperature of 1.5 °C and decrease in wind speed of 1 m s−1. The maximum impacts on atmospheric pollutants occur over parts of north and east China where emissions are greater, with an increase of 5 ppbv in NO2 and 25 ppbv in CO and a decrease of 10 ppbv in O3 and 4 ppbv in NO. This study also demonstrates the effects of the solar eclipse on surface photo-oxidants in different parts of China. Although the sun was obscured to a smaller extent in polluted areas than in clean areas, the impacts of the eclipse in polluted areas are greater and last longer than they do in clean areas. In contrast, the change in radical concentrations (OH, HO2 and NO3) in clean areas is much larger than in polluted areas mainly because of the limited source of radicals in these areas. The change in radical concentrations during the eclipse reveals that nighttime chemistry dominates in both clean and polluted areas. As solar eclipses provide a natural opportunity to test more thoroughly our understanding of atmospheric chemistry, especially that governed by photolysis, a comprehensive experimental campaign during a future solar eclipse is highly desirable.

Description: One-week integrated PM2.5 samples were collected over four years (2005–2008) at a pair of sites, one rural and one urban site, in the area of Beijing, China. Weekly organic and elemental carbon (OC and EC) concentrations from these samples were measured to investigate their atmospheric concentrations, temporal variation patterns and the factors influencing these aspects. A slightly systematic decrease in annual mean concentration of OC and an opposite trend for EC at both sites was observed. Since OC accounted for about 70 % of total carbon (TC, i.e. OC + EC) the total carbonaceous mass experienced a slight decline on a yearly basis over the study period. Its fraction of PM2.5 mass at the urban site in 2008 was significantly lower than observed 10 years earlier (1999), indicating that the relative importance of carbonaceous species in PM2.5 has decreased. In urban Beijing clear seasonal variations (by factors of 1.35 ~ 3.0) were shown in both OC and EC with higher weekly concentrations and fluctuations in winter and much lower values in summer and spring. The minimum seasonal urban excesses of OC (3.0 μg m−3) and EC (1.3 μg m−3) occurred in the summer of 2008, which were only one-ninth and one-seventh of their corresponding maximum values, respectively. This reduction in the urban-difference, coupled with more positive stable carbon isotope values of EC at the urban site in that summer relative to the preceding summers, supports that the special clean air campaign for the 2008 Summer Olympic Games very likely had noticeable impact on the ambient concentrations of carbonaceous aerosols in the Beijing area, particularly on the local urban scale. Less consistent seasonal patterns in OC and EC, their scattered correlation, and higher mass ratios of OC to EC (OC/EC) at the rural site indicate more complex and variable major sources regarding aerosol formation in the rural area. These emission sources include biomass burning during the harvest seasons, widely used high-polluting family stoves and small boilers for cooking and heating with high OC/EC ratios, and a greater relative quantity of secondary organic aerosols.

Description: Measurements of gaseous pollutants – including ozone (O3), sulfur dioxide (SO2), nitrogen oxides (NOX = NO + NO2), carbon monoxide (CO), particle number concentrations (5.6–560 nm and 0.47–30 μm) – and meteorological parameters (T, RH, P) were conducted during the Campaigns of Air Quality Research in Beijing and Surrounding Regions in 2008 (CAREBeijing-2008), from 27 August through 13 October 2008. The data from a total 18 flights (70 h flight time) from near the surface to 2100 m altitude were obtained with a Yun-12 aircraft in the southern surrounding areas of Beijing (38–40° N, 114–118° E). The objectives of these measurements were to characterize the regional variation of air pollution during and after the Olympics of 2008, determine the importance of air mass trajectories and to evaluate of other factors that influence the pollution characteristics. The results suggest that there are primarily four distinct sources that influenced the magnitude and properties of the pollutants in the measured region based on back-trajectory analysis: (1) southerly transport of air masses from regions with high pollutant emissions, (2) northerly and northeasterly transport of less pollutant air from further away, (3) easterly transport from maritime sources where emissions of gaseous pollutant are less than from the south but still high in particle concentrations, and (4) the transport of air that is a mixture from different regions; that is, the air at all altitudes measured by the aircraft was not all from the same sources. The relatively long-lived CO concentration is shown to be a possible transport tracer of long-range transport from the northwesterly direction, especially at the higher altitudes. Three factors that influenced the size distribution of particles – i.e., air mass transport direction, ground source emissions and meteorological influences – are also discussed.

Description: Global policies that regulate anthropogenic mercury emissions to the environment require quantitative and comprehensive source–receptor relationships for mercury emissions, transport and deposition among major continental regions. In this study, we use the GEOS-Chem global chemical transport model to establish source–receptor relationships among 11 major continental regions worldwide. Source–receptor relationships for surface mercury concentrations (SMC) show that some regions (e.g., East Asia, the Indian subcontinent, and Europe) should be responsible for their local surface Hg(II) and Hg(P) concentrations due to near-field transport and deposition contributions from their local anthropogenic emissions (up to 64 and 71% for Hg(II) and Hg(P), respectively, over East Asia). We define the region of primary influence (RPI) and the region of secondary influence (RSI) to establish intercontinental influence patterns. Results indicate that East Asia is the SMC RPI for almost all other regions, while Europe, Russia, and the Indian subcontinent also make some contributions to SMC over some receptor regions because they are dominant RSI source regions. Source–receptor relationships for mercury deposition show that approximately 16 and 17% of dry and wet deposition, respectively, over North America originate from East Asia, indicating that transpacific transport of East Asian emissions is the major foreign source of mercury deposition in North America. Europe, Southeast Asia, and the Indian subcontinent are also important mercury deposition sources for some receptor regions because they are the dominant RSIs. We also quantify seasonal variation on mercury deposition contributions over other regions from East Asia. Results show that mercury deposition (including dry and wet) contributions from East Asia over the Northern Hemisphere receptor regions (e.g., North America, Europe, Russia, the Middle East, and Middle Asia) vary seasonally, with the maximum values in summer and minimum values in winter. The opposite seasonal pattern occurs on mercury dry deposition contributions over Southeast Asia and the Indian subcontinent.