PM10 in the atmosphere and incidence of respiratory illness in Chiangmai during the smoggy pollution

Adverse health effects of atmospheric exposure to particles have been described in numerous epidemiological studies. In early of March 2007, there was a big environmental crisis in the northern area of Thailand. Smoggy pollution due to the fires covered many provinces in this area. Here, the author analyzes the correlation on incidence of respiratory illness and PM10 level in Chiangmai, a province in northern Thailand where the pollution occurred. The finding of emerging of the respiratory illness is similar to those previous reports on other smoggy pollutions due to fires. However, there is not a direct statistical significant relationship. It is proved that PM10 might be a risk for respiratory illness attack.     

Source apportionment and secondary organic aerosol estimation of PM2.5 in an urban atmosphere in China

PM2.5 is the key pollutant in atmospheric pollution in China.With new national air quality standards taking effect,PM2.5 has become a major issue for future pollution control.To effectively prevent and control PM2.5,its emission sources must be precisely and thoroughly understood.However,there are few publications reporting comprehensive and systematic results of PM2.5 source apportionment in the country.Based on PM2.5 sampling during 2009 in Shenzhen and follow-up investigation,positive matrix factorization(PMF)analysis has been carried out to understand the major sources and their temporal and spatial variations.The results show that in urban Shenzhen(University Town site),annual mean PM2.5 concentration was 42.2μg m?3,with secondary sulfate,vehicular emission,biomass burning and secondary nitrate as major sources;these contributed30.0%,26.9%,9.8%and 9.3%to total PM2.5,respectively.Other sources included high chloride,heavy oil combustion,sea salt,dust and the metallurgical industry,with contributions between 2%–4%.Spatiotemporal variations of various sources show that vehicular emission was mainly a local source,whereas secondary sulfate and biomass burning were mostly regional.Secondary nitrate had both local and regional sources.Identification of secondary organic aerosol(SOA)has always been difficult in aerosol source apportionment.In this study,the PMF model and organic carbon/elemental carbon(OC/EC)ratio method were combined to estimate SOA in PM2.5.The results show that in urban Shenzhen,annual SOA mass concentration was 7.5μg m?3,accounting for 57%of total organic matter,with precursors emitted from vehicles as the major source.This work can serve as a case study for further in-depth research on PM2.5 pollution and source apportionment in China.     

Average mass concentrations of TSP, PM10 and PM2.5 in Erzurum urban atmosphere, Turkey

In this study, particulate matters (TSP, PM₁₀, PM_2.5 and PM_10–2.5) which are hazardous for environment and human health were investigated in Erzurum urban atmosphere at a sampling point from February 2005 to February 2006. During sampling, two low volume samplers were used and each sampling period lasted approximately 24 h. In order for detection of representative sampling region and point of Erzurum, Kriging method was applied to the black smoke concentration data for winter seasons. Mass concentrations of TSP, PM₁₀ and PM_2.5 of Erzurum urban atmosphere were measured on average, as 129, 31 and 13 μg/m³, respectively, in the sampling period. Meteorological factors, such as temperature, wind speed, wind direction and rainfall were typically found to be affecting PMs, especially PM_2.5. Air temperature did not seem to be significantly affecting TSP and PM₁₀ mass concentrations, but had a considerably negative induction on PM_2.5 mass concentrations. However, combustion sourced PM_2.5 was usually diluted from the urban atmosphere by the speed of wind, soil sourced coarse mode particle concentrations (TSP, PM₁₀) were slightly affected by the speed of wind. Rainfall was found to be decreasing concentrations to 48% in all fractions (TSP, PM₁₀, PM_10–2.5, PM_2.5) and played an important role on dilution of the atmosphere. Fine mode fraction of PM (PM_2.5) showed significant daily and seasonal variations on mass concentrations. On the other hand, coarse mode fractions (TSP, PM₁₀ and PM_10–2.5) revealed more steady variations. It was observed that fine mode fraction variations were affected by the heating in residences during winter seasons.     

Correlation between plasmid DNA damage induced by PM_(10) and trace metals in inhalable particulate matters in Beijing air

Based on the study of Beijing PM10 bioreactivity with the newly developed plasmid DNA assay method, and analysis for trace elements of PM10, the cause of plasmid DNA damage by PM10 was investigated. The study showed that plasmid DNA oxidative damages by PM10 are of difference in different seasons at various areas. The concentrations of TM50 of PM10 in whole samples respectively collected at urban and comparison sites during winter were 900 μg mL?1 and 74 μg mL?1, while those in their corresponding soluble fractions were 540 μg mL?1 and 86 μg mL?1. In contrast, TM50 contents of PM10 from summer whole samples at urban areas and comparison sites were 116 μg mL?1 and 210 μg mL?1, whereas those in their soluble fractions were 180 μg mL?1 and 306 μg mL?1. The difference of bioreactivity of Beijing PM10 resulted from the variation of trace elements. The oxidative damage of plasmid DNA caused by Pb, Zn, As in PM10 (whole sample) was relatively strong. TM50 and Mn, V, Zn display stronger correlation in the soluble fraction. It implies that Zn could be the major trace element in Beijing PM10 which contributes to oxidative damage to plasmid DNA.     

Fine Particles (PM2.5) in Residential Areas of Lucknow City and Factors Influencing the Concentration

Urban populations are exposed to a high level of fine and ultrafine particles from motor vehicle emissions which affect human health. To assess the hourly variation of fine particle (PM_2.5) concentration and the influence of temperature and relative humidity (RH) on the ambient air of Lucknow city, monitoring of PM_2.5 along with temperature and RH was carried out at two residential locations, namely Vikas Nagar and Alambagh, during November 2005. The 24 h mean PM_2.5 concentration at Alambagh was 131.74 μg/m³ and showed an increase of 13.74%, which was significantly higher (p < 0.05) than the Vikas Nagar level. The 24 h mean PM_2.5 on weekdays for both locations was found to be 142.74 μg/m³ (an increase of 66.23%) which was significantly higher (p < 0.01) than the weekend value, indicating that vehicular pollution is one of the important sources of PM_2.5. The mean PM_2.5 at night for all the monitoring days was 157.69 μg/m³ and was significantly higher (p < 0.01) than the daytime concentration (89.87 μg/m³). Correlation and multiple regressions showed that the independent variables, i. e., time, temperature, and RH together accounted for 54%, whereas RH alone accounted for 53% of total variations of PM_2.5, suggesting that RH is the best influencing variable to predict the PM_2.5 concentration in the urban area of Lucknow city. The 24 h mean PM_2.5 for all the monitoring days was found to be higher than the NAAQS recommended by the US‐EPA (65 μg/m³) and can be considered to be an alarming indicator of adverse health effects for city dwellers.     

Spatial character of the gaseous and particulate state compound correlation of urban atmospheric pollution in winter and summer

The spatial/temporal variation information of atmospheric dynamic-chemical processes at observation site points of the "canopy" boundary of Beijing urban building ensemble and over urban area "surface", as well as the seasonal correlation structure of the gaseous and particulate states of urban atmospheric pollution (UAP) and its seasonal conversion feature at observation points are investigated, using the comprehensive observation data of the Beijing City Air Pollution Observation Experiment (BECAPEX) in winter and summer 2003 with a "point-surface" combined research approach. By using "one dimension spatial empirical orthogonal function (EOF)" principal component analysis (PCA) mode, the seasonal change of gaseous and particulate states of atmospheric aerosols and the association feature of pollutant species under the background of the complicated structure of urban boundary layer (UBL) are analyzed. The comprehensive analyses of the principal components of particle concentrations,gaseous pollutant species, and meteorological conditions reveal the seasonal changes of the complex constituent and structure features of the gaseous and particulate states of UAP to further trace the impact feature of urban aerosol pollution surface sources and the seasonal difference of the component structure of UAP. Research results suggest that in the temporal evolution of the gaseous and particulate states of winter/summer UAP, NOx, CO, and SO2 showed an "in-phase" evolution feature, however, O3 showed an "inverse-phase" relation with other species,all possessing distinctive dependent feature. On the whole, summer concentrations of gaseous pollutants CO, SO2, and NOx were obviously lower than winter ones, especially, the reduction in CO concentration was most distinctive, and ones in SO2 and NOx were next. However, the summer O3 concentration was more than twice winter one. Winter/summer differences in PM10and PM2.5 particle concentrations were relatively not obvious, which indicates that responses of PM10 and PM2.5 particle concentrations to the difference of winter/summer heating period emission sources are far less distinctive than those of NOx, SO2, and CO. The correlation feature of winter/summer gaseous and particulate states depicts that both PM10 and PM2.5 particles were significantly correlated with NOx, and their correlations with NOx are more significant than those with other pollutants. Through PCA, it is found that there was a distinctive difference in the principal component combination structure of winter/summer PM10 and PM2.5 particles: SO2 and NOx dominated in the principal component of winter PM10 and PM2.5 particles; while CO and NOx played the major role in the principal component of summer PM10 and PM2.5 particles. For winter/summer PM10 and PM2.5 particles, there might exist the gaseous and particulate states correlation structures of different "combinations" of such dependent pollutant species. Research results also uncover that the interaction processes of gaseous and particulate states were also related with the vertical structure of UBL, that is to say, the low value layer of UBL O3 concentration was associated with the collocation of atmospheric vertical structures of the low level inversion,inverse humidity, and small wind, which depicts summer boundary layer atmospheric character, i.e.the compound impact of the dependent factor "combination" of wind, temperature, and humidity elements and their collocation structure on the variations of different gaseous pollutant concentrations. Such a depth structure of the extremely low value of O3 concentration in the UBL accords with its "inverse-phase" relation with other gaseous pollutant species. The PCA of meteorological factors associated with PM10 and PM2.5 concentrations also reveals the sensitivity of PM10 and PM2.5 concentration to the combinatory feature of local meteorological conditions.