scholarly journals Supplementary material to "Diurnal and day-to-day characteristics of ambient particle mass size distributions from HR-ToF-AMS measurements at an urban site and a suburban site in Hong Kong"

Author(s):  
Berto P. Lee ◽  
Hao Wang ◽  
Chak K. Chan
2017 ◽  
Vol 17 (22) ◽  
pp. 13605-13624 ◽  
Author(s):  
Berto Paul Lee ◽  
Hao Wang ◽  
Chak Keung Chan

Abstract. Mass-concentration-based particle size distributions measured by a high-resolution aerosol mass spectrometer were systematically analyzed to assess long and short-term temporal characteristics of ambient particle size distributions sampled at a typical urban environment close to emission sources and a suburban coastal site representing a regional and local pollution receptor location in Hong Kong. Measured distributions were bimodal and deconvoluted into submodes, which were analyzed for day-to-day variations and diurnal variations. Traffic and cooking emissions at the urban site contributed substantially to particle mass in both modes, while notable decreases in mass median diameters were limited to the morning rush hour. Inorganic particle components displayed varying diurnal behavior, including nocturnal nitrate formation and daytime photochemical formation evident in both modes. Suburban particle size distributions exhibited notable seasonal disparities with differing influence of local formation, particularly in spring and summer, and transport which dominated in the fall season leading to notably higher sulfate and organic accumulation-mode particle concentrations. Variations in particle mixing state were evaluated by comparison of interspecies mass median diameter trends at both measurement sites. Internal mixing was prevalent in the accumulation mode in spring at the urban site, while greater frequency of time periods with external mixing of particle populations comprising different fractions of organic constituents was observed in summer. At the suburban site, sulfate and nitrate in the accumulation mode more frequently exhibited differing particle size distributions in all seasons, signifying a greater extent of external mixing. At the urban site, periods of greater submicron inorganic mass concentrations were more likely to be caused by increases in both Aitken- and accumulation-mode particle mass in summer, while at the suburban receptor location, organic and nitrate Aitken-mode particle mass contributed more regularly to higher total submicron species mass concentrations in most seasons (spring, summer, and winter).


2017 ◽  
Author(s):  
Berto P. Lee ◽  
Hao Wang ◽  
Chak K. Chan

Abstract. Mass concentration based particle size distributions measured by a high-resolution aerosol mass spectrometer were systematically analyzed to assess long and short-term temporal characteristics of ambient particle size distributions sampled at a typical urban environment close to emission sources and a suburban coastal site representing a regional and local pollution receptor location in Hong Kong. Measured distributions were bimodal and deconvoluted into submodes which were analyzed for day-to-day variations and diurnal variations. Traffic and cooking emissions at the urban site contributed substantially to particle mass in both modes, while notable decreases in mass median diameters were limited to the morning rush hour. Inorganic particle components displayed varying diurnal behavior, including nocturnal nitrate formation and daytime photochemical formation evident in both modes. Suburban particle size distributions exhibited notable seasonal disparities with differing influence of local formation, particularly in spring and summer, and transport which dominated in the fall season leading to notably higher sulfate and organic accumulation mode particle concentrations. Variations in particle mixing state were evaluated by comparison of inter-species mass median diameter trends at both measurement sites. Internal mixing was prevalent in the accumulation mode in spring at the urban site, while greater frequency of time periods with external mixing of particle populations comprising different fractions of organic constituents was observed in summer. At the suburban site, sulfate and nitrate in the accumulation mode more frequently exhibited differing particle size distributions in all seasons signifying a greater extent of external mixing. At the urban site, periods of greater submicron inorganic mass concentrations were more likely to be caused by increases in both Aitken and accumulation mode particle mass in summer, while at the suburban receptor location organic and nitrate Aitken mode particle mass contributed more regularly to higher total submicron species mass concentrations in most seasons (spring, summer and winter).


2015 ◽  
Vol 15 (17) ◽  
pp. 10219-10237 ◽  
Author(s):  
M. Pikridas ◽  
J. Sciare ◽  
F. Freutel ◽  
S. Crumeyrolle ◽  
S.-L. von der Weiden-Reinmüller ◽  
...  

Abstract. Ambient particle number size distributions were measured in Paris, France, during summer (1–31 July 2009) and winter (15 January to 15 February 2010) at three fixed ground sites and using two mobile laboratories and one airplane. The campaigns were part of the Megacities: Emissions, urban, regional and Global Atmospheric POLlution and climate effects, and Integrated tools for assessment and mitigation (MEGAPOLI) project. New particle formation (NPF) was observed only during summer on approximately 50 % of the campaign days, assisted by the low condensation sink (about 10.7 ± 5.9 × 10−3 s−1). NPF events inside the Paris plume were also observed at 600 m altitude onboard an aircraft simultaneously with regional events identified on the ground. Increased particle number concentrations were measured aloft also outside of the Paris plume at the same altitude, and were attributed to NPF. The Paris plume was identified, based on increased particle number and black carbon concentration, up to 200 km away from the Paris center during summer. The number concentration of particles with diameters exceeding 2.5 nm measured on the surface at the Paris center was on average 6.9 ± 8.7 × 104 and 12.1 ± 8.6 × 104 cm−3 during summer and winter, respectively, and was found to decrease exponentially with distance from Paris. However, further than 30 km from the city center, the particle number concentration at the surface was similar during both campaigns. During summer, one suburban site in the NE was not significantly affected by Paris emissions due to higher background number concentrations, while the particle number concentration at the second suburban site in the SW increased by a factor of 3 when it was downwind of Paris.


2015 ◽  
Vol 15 (4) ◽  
pp. 5663-5712 ◽  
Author(s):  
M. Pikridas ◽  
J. Sciare ◽  
F. Freutel ◽  
S. Crumeyrolle ◽  
S.-L. von der Weiden-Reinmüller ◽  
...  

Abstract. Ambient particle number size distributions were measured in Paris, France during summer (1–31 July 2009) and winter (15 January–15 February 2010) at three fixed ground sites and using two mobile laboratories and one airplane. The campaigns were part of the MEGAPOLI project. New particle formation (NPF) was observed only during summer at approximately 50% of the campaign days, assisted by the low condensation sink (about 10.7 ± 5.9 × 10−3 s−1). NPF events inside the Paris plume were also observed at 600 m altitude onboard an aircraft simultaneously with regional events identified on the ground. Increased particle number concentrations were measured aloft also outside of the Paris plume at the same altitude, and were attributed to NPF. The Paris plume was identified, based on increased particle number and black carbon concentration, up to 200 km away from Paris center during summer. The number concentration of particles with diameter exceeding 2.5 nm measured on the surface at Paris center was on average 6.9 ± 8.7 × 104 and 12.1 ± 8.6 × 104 cm−3 during summer and winter, respectively, and was found to decrease exponentially with distance from Paris. However, further than 30 km from the city center, the particle number concentration at the surface was similar during both campaigns. During summer one suburban site in the NE was not significantly affected by Paris emissions due to higher background number concentrations, while the particle number concentration at the second suburban site in the SW increased by a factor of three when it was downwind of Paris.


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