ALBERT

Description: We present measurement results of trace gaseous pollutants obtained at the Shangdianzi (SDZ) Global Atmosphere Watch (GAW) regional station in Northern China, from September 2003 to December 2006. The gases include ozone (O3), nitrogen oxide(s) (NOx=NO+NO2), sulfur dioxide (SO2), and carbon monoxide (CO). During the study period, the mean annual O3 concentrations were 30.1±21.0, 32.8±19.1 and 30.9±19.8 ppbv in 2004, 2005 and 2006. The corresponding NOx values were 14.5±14.0, 11.0±11.3 and 12.7±11.8 ppbv, respectively. The mean annual SO2 concentrations were 5.9±10.0, 6.1±9.9 and 7.6±10.2 ppbv in 2004, 2005 and 2006, while the mean CO levels were 586±415 and 742±558 ppbv in 2005 and 2006. The data obtained at SDZ station are compared with the results measured at other background sites in China as well as abroad. The concentrations of O3, NOx, SO2, and CO at the SDZ background station are found to have clear seasonal and diurnal variations. The impacts of local and remote pollution sources on the regional air quality are assessed using trace gases concentration roses and 3-day back trajectories of air masses arriving at the SDZ station.

Description: Sea-land and mount-valley circulations are the dominant mesoscale synoptic systems affecting the Beijing area during summertime. Under the influence of these two circulations, the prevailing wind is southwesterly from afternoon to midnight, and then changes to northeasterly till forenoon. In this study, surface ozone (O3), carbon monoxide (CO), nitric oxide (NO), nitrogen dioxide (NO2), nitrogen oxide (NOx) and non-methane hydrocarbons (NMHCs) were measured at four sites located along the route of prevailing wind, including two upwind urban sites (Fengtai "FT" and Baolian "BL"), an upwind suburban site (Shunyi "SY") and a downwind rural site (Shangdianzi "SDZ") during 20 June–16 September 2007. The purpose is to improve our understanding of ozone photochemistry in urban and rural areas of Beijing and the influence of urban plumes on ozone pollution in downwind rural areas. It is found that ozone pollution was synchronism in the urban and rural areas of Beijing, coinciding with the regional-scale synoptic processes. Due to the high traffic density and local emissions, the average levels of reactive gases NOx and NMHCs at the non-rural sites were much higher than those at SDZ. The level of long-lived gas CO at SDZ was comparable to, though slightly lower than, at the urban sites. We estimate the photochemical reactivity (LOH and the ozone formation potential (OFP) in the urban (BL) and rural (SDZ) areas using measured CO and NMHCs. The OH loss rate coefficient (LOH by total NMHCs at the BL and SDZ sites are estimated to be 50.7 s-1 and 15.8 s-1, respectively. While alkenes make a major contribution to the LOH, aromatics dominate OFP at both urban and rural sites. With respect to the individual species, CO has the largest ozone formation potential at the rural site, and at the urban site aromatic species are the leading contributors. While the O3 diurnal variations at the four sites are typical for polluted areas, the ozone peak values are found to lag behind one site after another along the route of prevailing wind from SW to NE. Intersection analyses of trace gases reveal that polluted air masses arriving at SDZ were more aged with both higher O3 and Ox concentrations than those at BL. The results indicate that urban plume can transport not only O3 but its precursors, the latter leading more photochemical O3 production when being mixed with background atmosphere in the downwind rural area.

Description: Sea-land and mount-valley circulations are the dominant mesoscale synoptic systems affecting the Beijing area during summertime. Under the influence of these two circulations, the prevailing wind is southwesterly from afternoon to midnight, and then changes to northeasterly till forenoon. In this study, surface ozone (O3), carbon monoxide (CO), nitric oxide (NO), nitrogen dioxide (NO2), nitrogen oxide (NOx) and non-methane hydrocarbons (NMHCs) were measured at four sites located along the route of prevailing wind, including two upwind urban sites (Fengtai (FT) and Baolian (BL)), an upwind suburban site (Shunyi (SY)) and a downwind rural site (Shangdianzi (SDZ)) during 20 June–16 September 2007. The purpose is to improve our understanding of ozone photochemistry in urban and rural areas of Beijing and the influence of urban plumes on ozone pollution in downwind rural areas. It is found that ozone pollution was synchronism in the urban and rural areas of Beijing, coinciding with the regional-scale synoptic processes. Due to the high traffic density and local emissions, the average levels of reactive gases NOx and NMHCs at the non-rural sites were much higher than those at SDZ. The level of long-lived gas CO at SDZ was comparable to and slightly lower than it was at other sites. The daily-averaged ozone concentration at SDZ was much higher than at other sites due to weak titration. Ranking by OH loss rate coefficient (LOH), alkenes played a dominant role in total NMHCs reactivity at both urban and rural sites during the experiment, accounting for 48.6 % and 52.1 % of total LOH, respectively. The NMHCs data were also used to estimate the ozone potential formation (OFP) in Beijing. The leading contributors to ozone formation were aromatics at both urban and rural sites during the experiment, which accounts for 55.5 % and 49.4 % of total OFP, respectively. The ozone peak values are found to lag behind one site after another along the route of prevailing wind from SW to NE. Intersection analyses of trace gases reveal that polluted air masses arriving at SDZ were more aged with both higher O3 and Ox concentrations than those at BL. The results indicate that urban plume can transport not only O3 but its precursors, the latter leading more photochemical O3 production when being mixed with background atmosphere in the downwind rural area.

Description: Measurements of trace gaseous pollutants were taken at the Shangdianzi site, a WMO Global Atmosphere Watch (GAW) background station in Northern China. The results are presented for the period from September 2003 to December 2006. Seasonal and diurnal variations of the O3, NOx, SO2, and CO concentration are characterized and possible causes for them are discussed. The observed levels of the trace gases are comparable to those at some other background sites in polluted regions inside and outside of China. It was shown that the seasonal variation of O3 can change slightly from year to year due to the year-to-year alternation in the meteorological conditions. Higher CO concentrations were observed in some warmer months, particularly in June and July, 2006. Intensive biomass burning in the North China Plain region, in combination with the transport of regional pollution by more frequent southwesterly winds, is believed to be responsible for the elevated CO concentrations. The diurnal variation of O3, with delayed peaking times, suggests that the transport of photochemical aged plume is an important source for O3 at Shangdianzi. The diurnal variations of SO2 in all seasons show higher values during daytime, contradicting the common view. An explanation for this unusual phenomenon is hypothesized. To gain an insight into the impact of transport on the trace gases levels at Shangdianzi, air mass backward trajectories were calculated and analyzed in combination with corresponding pollutant concentrations. The results indicate that the transport of air masses from the North China Plain region and from the major coal mining regions west of Shangdianzi is responsible for the high concentrations of the gaseous pollutants.

Description: Regional ozone pollution has become one of the top environmental concerns in China, especially in those economically vibrant and densely populated regions, such as North China region including Beijing. To address this issue, surface ozone and ancillary data over the period 2004–2006 from the Shangdianzi Regional Background Station in north China were analyzed. Due to the suitable location and valley topography of the site, transport of pollutants from the North China Plain was easily observed and quantified according to surface wind directions. Regional (polluted) and natural (clean) background ozone concentrations were obtained by detailed statistic analysis. Contribution of pollutants from North China Plain to surface ozone at SDZ was estimated by comparing ozone concentrations observed under SW wind conditions and that under NE wind conditions. The average daily accumulated ozone contribution was estimated to be 240 ppb·hr. The average regional contributions to surface ozone at SDZ from the North China Plain were 21.8 ppb for the whole year, and 19.2, 28.9, 25.0, and 10.0 ppb for spring, summer, autumn, and winter, respectively. The strong ozone contribution in summer led to disappearance of the spring ozone maximum phenomenon at SDZ under winds other than from the WNN to E sectors. High winter NOx concentrations in the North China Plain caused negative ozone contribution in winter.

Description: Information about the long-term trends of surface and tropospheric ozone is important for assessing the impact of ozone on human health, vegetation, and climate. Long-term measurements from East Asia, especially China's eastern provinces, are urgently needed to evaluate potential changes of tropospheric ozone over this economically rapid developing region. In this paper, surface ozone data from the Linan Regional Background Station in eastern China are analyzed and results about the long-term trends of surface ozone at the station are presented. Surface ozone data were collected at Linan during 6 periods between August 1991 and July 2006. The seasonality and the long-term changes of surface ozone at the site are discussed, with focus on changes in the diurnal variations, the extreme values, and the ozone distribution. Some long-term trends of surface ozone, e.g., decrease in the average concentration, increase in the daily amplitude of the relative diurnal variations, increase in the monthly highest 5% of the ozone concentration, decrease in the monthly lowest 5% of the ozone concentration, increase in the frequencies at the high and low ends of the ozone distribution have been uncovered by the analysis. All the trends indicate that the variability of surface ozone has been enhanced. Possible causes for the observed trends are discussed. The most likely cause is believed to be the increase of NOx concentration.

Description: Windsor (Ontario) – the automotive capital of Canada does not have any significant mercury (Hg) sources. However, Windsor experiences trans-boundary air pollution as it is located immediately downwind of industrialized regions of the United States of America. A study was conducted in 2007 aimed to identify the potential regional sources of total gaseous mercury (TGM) and investigate the effects of regional sources and other factors on seasonal variability of TGM concentrations in Windsor. TGM concentration was measured at the University of Windsor campus using a Tekran® 2537A Hg vapour analyzer. An annual mean of 2.02±1.63 ng/m3 was observed in 2007. The average TGM concentration was high in the summer (2.48 ng/m3) and winter (2.17 ng/m3), compared to spring (1.88 ng/m3) and fall (1.76 ng/m3). Hybrid receptor modeling potential source contribution function (PSCF) was used by incorporating 72-h backward trajectories and measurements of TGM in Windsor. The results of PSCF were analyzed in conjunction with the Hg emissions inventory of North America (by state/province) to identify regions affecting Windsor. In addition to annual modeling, seasonal PSCF modeling was also conducted. The potential source region was identified between 24–61° N and 51–143° W. Annual PSCF modeling identified major sources southwest of Windsor, stretching from Ohio to Texas. The emissions inventory also supported the findings, as Hg emissions were high in those regions. Results of seasonal PSCF modeling were analyzed to find the combined effects of regional sources, meteorological conditions, and surface reemissions, on intra-annual variability of Hg concentrations. It was found that the summer and winter highs of atmospheric Hg can be attributed to areas where large numbers of coal fired power plants are located in the USA. Weak atmospheric dispersion due to low winds and high reemission from surfaces due to higher temperatures contributed to high concentrations in the summer. In the winter, the atmospheric removal of Hg was slow, but strong winds led to more dispersion, resulting in lower concentrations than the summer. Future studies could use smaller grid sizes and refined emission inventories, for more accurate analysis of source-receptor relationship of atmospheric Hg. Abbreviations of states/provinces: Alabama (AL), Arkansas (AR), British Columbia (BC), Georgia (GA), Iowa (IA), Illinois (IL), Indiana (IN), Kentucky (KY), Louisiana (LA), Manitoba (MB), Michigan (MI), Minnesota (MN), Mississippi (MS), Missouri (MO), Newfoundland and Labrador (NL), Ohio (OH), Ontario (ON), Oregon (OR), Pennsylvania (PA), Tennessee (TN), Texas (TX), West Virginia (WV), Wisconsin (WI).

Description: Turbulent fluxes of carbonyl sulfide (COS) and carbon disulfide (CS2) were measured over a spruce forest in Central Germany using the relaxed eddy accumulation (REA) technique. A REA sampler was developed and validated using simultaneous measurements of CO2 fluxes by REA and by eddy correlation. REA measurements were conducted during six campaigns covering spring, summer, and fall between 1997 and 1999. Both uptake and emission of COS and CS2 by the forest were observed, with deposition occurring mainly during the sunlit period and emission mainly during the dark period. On the average, however, the forest acts as a sink for both gases. The average fluxes for COS and CS2 are  -93 ± 11.7 pmol m-2 s-1 and  -18 ± 7.6 pmol m-2 s-1, respectively. The fluxes of both gases appear to be correlated to photosynthetically active radiation and to the CO2 and H2O fluxes, supporting the idea that the air-vegetation exchange of both gases is controlled by stomata. An uptake ratio COS/CO2 of 10 ± 1.7 pmol μmol-1 has been derived from the regression line for the correlation between the COS and CO2 fluxes. This uptake ratio, if representative for the global terrestrial net primary production, would correspond to a sink of 2.3 ± 0.5 Tg COS yr-1.

Description: Regional ozone pollution has become one of the top environmental concerns in China, especially in those economically vibrant and densely populated regions, such as North China region including Beijing. To address this issue, surface ozone and ancillary data over the period 2004–2006 from the Shangdianzi Regional Background Station in north China were analyzed. Due to the suitable location and valley topography of the site, transport of pollutants from the North China Plain was easily observed and quantified according to surface wind directions. Regional (polluted) and background (clean) ozone concentrations were obtained by detailed statistic analysis. Contribution of pollutants from North China Plain to surface ozone at SDZ was estimated by comparing ozone concentrations observed under SW wind conditions and that under NE wind conditions. The average daily accumulated ozone contribution was estimated to be 240 ppb·hr. The average regional contributions to surface ozone at SDZ from the North China Plain were 21.8 ppb for the whole year, and 19.2, 28.9, 25.0, and 10.0 ppb for spring, summer, autumn, and winter, respectively. The strong ozone contribution in summer led to disappearance of the spring ozone maximum phenomenon at SDZ under winds other than from the NNW to E sectors. The emissions of nitrogen oxide in the North China plain cause a decrease in ozone concentrations in winter.

Description: The acidity of precipitation has been observed at stations of the Acid Rain Monitoring Network run by the China Meteorological Administration (CMA-ARMN) since 1992. Previous studies have shown that different long-term trends exist in different regions but detailed analysis of the causes of these is lacking. In this paper, we analyze summertime precipitation acidity data from the CMA-ARMN during 1992–2006 using EOFs and show that the summertime pH in China had different trends before and after 2000. The most significant decrease of pH is found in Central China. To investigate the causes of this decrease of pH in summer, we explore the relationship between changes in the pH value, the East Asian summer monsoon index, rainfall data, and pollutants emissions. We find that the East Asian summer monsoon can significantly affect the acidity of summer precipitation in Central China. In strong monsoon years, the pH in Central China is about 0.33 lower than that in weak monsoon years. Chemical transport model simulations using fixed emissions indicate that about 65% of the pH value difference (i.e., 0.22) is related to the summer monsoon, and constitutes 18–36% of the observed pH change (0.6∼1.2) in Central China during 1992–2006. Further studies reveal a relationship between the pH in Central China and the rainfall in the middle and lower reaches of the Yangtze River (MLYR), which can explain about 24% of the variance of pH in Central China. Simulations using an annually varying emission inventory show that at least 60% of the variation in precipitation acidity in Central China can be attributed to changes in pollutant emissions. Therefore, the increase in emissions of acidic species is the most important cause for the observed decrease of pH in Central China, and changes in meteorological factors, such as rainfall and other parameters related to the East Asian summer monsoon, play a less important but still significant role.