Polycyclic Aromatic Hydrocarbons In Winter Research Articles

Seasonal variation, source identification, and health risk assessment of atmospheric polycyclic aromatic hydrocarbons (PAHs) in Ulsan, South Korea

Gaseous and particulate 21 PAHs were monitored at a residential site in Ulsan, South Korea, over three seasons (December 2013–August 2014). The mean concentrations of Σ21 PAHs were highest in winter (16.2 ± 8.2 ng/m3), followed by spring (8.37 ± 4.53 ng/m3) and summer (6.23 ± 2.53 ng/m3). The mean gaseous concentration of Σ21 PAHs (7.39 ± 4.39 ng/m3) was 2.7 times higher than that of particulate PAHs (2.70 ± 3.38 ng/m3). To identify the sources of PAHs (both types of sources and their areas), diagnostic ratios, principal component analysis, and concentration-weighted trajectory (CWT) were used. The results showed that pyrogenic sources (e.g., coal combustion) were the primary emission sources of PAHs in winter and spring. In summer, the influence of both coal and heavy oil combustion was dominant, suggesting that PAHs could be transported from industrial areas of Ulsan (e.g., petrochemical and nonferrous industrial complexes) by seasonal winds. Regarding emission source areas, the CWT analysis revealed that in winter and spring, PAHs in Ulsan could be attributed to emissions from regional areas, e.g., China and North Korea. The PAH concentrations were also used to assess the health risks associated with the inhalation of these compounds for adults aged 18–70. The results showed that the cancer risks from Σ19 PAHs and Σ13 PAHs did not exceed the guideline set by the US EPA (10−6), indicating no cancer risks for this target group. However, it is worth noting that certain PAHs, which are not listed as priority PAHs by the US EPA, make significant contributions to the benzo[a]pyrene equivalent and the associated cancer risks. Therefore, it is necessary to investigate not only the priority PAHs but also other PAH species to fully evaluate their effect on human health.

Air‐Sea Gas Exchange and Its Potential Influence on the Regional Fate of Polycyclic Aromatic Hydrocarbons in the East China Marginal Sea

AbstractTo investigate the air‐sea gas exchange and its potential influence on the regional fate of polycyclic aromatic hydrocarbons (PAHs) in the East China Marginal Seas (ECMS), which consist of the East China Sea (ECS) and Yellow Sea (YS), we collected air and surface seawater samples of this area in the summer 2018 and winter 2019, respectively. Generally, PAHs underwent a strong volatilization process in the ECMS in both summer and winter. Good correlations between wind speed and the magnitude of air‐sea gas exchange were found for low molecular weight PAHs, suggesting the rate of their air‐sea gas exchange was influenced by the static stability of overlying atmosphere. However, such an influence for high molecular weight PAHs was constrained by their low Henry's law constant. Dissolved concentration of PAHs in surface seawater was another key factor regulating their air‐sea gas exchange, which not only influenced the rate of air‐sea gas exchange but also was involved in the exchange direction. Higher air‐sea gas exchange fluxes of PAHs in winter were attributed to their increasing dissolved concentrations in seawater during this season. A mass conservation analysis revealed a huge volatilization loss of PAHs from seawater to atmosphere, suggesting air‐sea gas exchange might be a key process to modulate the distribution and occurrence of PAHs in the ECS and YS. Such a loss of PAHs in seawater might be compensated by the sediment resuspension, which implied that the sedimentary deposit could serve as a secondary source of PAHs in seawater and overlying atmosphere.

Molecular Composition, Seasonal Variation, and Size Distribution of n-Alkanes, PAHs, and Saccharides in a Medium-Sized City of Guanzhong Plain, Northwest China: Evaluation of Control Measures Executed in the Past Decade

Baoji is a medium-sized city in the Guanzhong Plain of northwest China. The compositions of three important organic groups, namely n-alkanes, polycyclic aromatic hydrocarbons (PAHs), and saccharides in atmospheric aerosol with different aerodynamic diameters in power were determined. Both seasonal and daily trends of the target organic chemical groups were demonstrated. The concentration levels of total quantified n-alkanes and saccharides in total suspended particles (TSP) in winter were 541 ± 39 and 651 ± 74 ng·m-3, respectively, much higher than those of the other three seasons. A high total quantified PAHs concentration level of 59.6 ± 6.4 ng·m-3 was also seen in wintertime. n-Alkanes showed a bimodal percent distribution in spring, autumn, and winter. Two peaks were found with the particle sizes of 0.7 μm < Dp < 2.1 μm and 3.3 μm < Dp < 4.7 μm, respectively. In summer, a unimodal was seen with a peak of 4.7 μm < Dp < 5.8 μm. Dehydrated saccharides and PAHs present a unimodal size distribution peaking at the aerodynamic diameters of 0.7 µm < Dp < 2.1 µm. In contrast to glucose and fructose, they mainly exist in the coarse mode particles and have the highest concentrations at aerodynamic diameters of 4.7 µm < Dp < 9.0 µm. The geometric mean diameters (GMD) of n-alkanes and saccharides of the fine particles in winter were higher than in the other seasons. Compared with the data in 2008, the fossil fuel-derived n-alkanes and PAHs in winter decreased by nearly an order of magnitude in 2017. Both the carbon preference index (CPI) of n-alkanes and the diagnostic ratios of PAHs suggest that coal combustion and vehicle exhaust were the major pollution sources of the organic groups in the two decades. It should be noted that the contribution of traffic emissions greatly increased from 2008 to 2017, consistently with a large raise of registered vehicles in Baoji city. The overall results confirm that the control measures conducted by the local government in the recent decade mitigated the air pollution in this city.

A comprehensive evaluation of PM2.5-bound PAHs and their derivative in winter from six megacities in China: Insight the source-dependent health risk and secondary reactions.

Atmospheric PAHs (polycyclic aromatic hydrocarbons) and their derivatives are a global concern that influences environments and threatens human health. Concentrations of 52 PAHs and the main derivatives in six Chinese megacities were measured in the winter of 2019. The concentrations of ∑PAHs (sum of 52 PAHs) ranged from 19.42±7.68 to 65.40±29.84ngm-3, with significantly higher levels in northern cities (Harbin [HB], Beijing [BJ], and Xi'an [XA]) than southern ones (Wuhan [WH], Chengdu [CD] and Guangzhou [GZ]). Source apportionment of ∑PAHs was conducted by the PMF model and results showed coal combustion and traffic emissions were the two dominant sources, which dominated ∑PAHs in northern and southern cities, respectively. Biomass burning was also characterized as a crucial source of ∑PAHs and showed extremely high contributions in XA (42.5%). Assisted by the individual PAH source apportionment results, the source-depend TEQ (total BaP equivalent) and incremental lifetime cancer risk (ILCR) were firstly reported in these cities. The results highlighted the contributions of coal combustion and biomass burning to both TEQ and ILCR, which were underestimated by ∑PAHs source apportionment. Secondary organic aerosol-derived PAHs were demonstrated to increase the TEQ compared with the fresh PAHs and three parameters, namely temperature, relative humidity, and O3 concentrations were characterized by multiple linear regression as the principal factors influencing secondary reactions of PAHs in winter. This study provides accurate human health-orientated results and potential control measures to mitigate the toxicity of secondary formed PAHs, and significantly decrease the uncertainty level of traditional methods. The results also revealed great progress in air pollution control by the Chinese government in the past 20years, but still a long way to go to formulate strict emission control strategies from both environmental and human health-protective perspectives.

Polycyclic aromatic hydrocarbons (PAHs) in gas, PM2.5, and frost samples in a severely polluted rural site of the North China Plain: Distribution, source, and risk assessment

The process of frost formation has been studied as an important deposition pathway for removing atmospheric pollutants. However, the removal of organic species during frost formation remains unknown. Gas, PM2.5 and frost samples were collected in Wangdu, a severely polluted rural site in the North China Plain, during the winter of 2018. The concentrations, distributions, sources, and ecological and health risks of the 16 PAHs in the samples were determined. The 24 h-averaged concentrations of PAHs in the air (gas + PM2.5) reached 719 ng m−3, indicating that the local atmosphere was heavily contaminated by PAHs in winter. The average concentrations of PAHs in the frost insoluble reached 27.5 μg g−1, indicating the strong ambient PAHs deposition during the frost process. The distribution patterns of individual PAH species indicated that the PAHs in the gas influenced the frost samples, and the sources of PAHs in frost samples were highly similar to those in PM2.5 samples. The calculated lifetime lung cancer risk (LLCR) via inhalation of ambient PAHs was classified as high risks. The average total Benzo(a)pyrene toxic equivalent quotient (TEQ) of PAHs in the frost samples was estimated as 2.50 μg TEQ g−1, posing a high threat to the ecological environment and health. After the melting of frost, the PAHs are released into the soil. Although the concentrations are diluted, the PAH concentrations could adversely affect the growing vegetation or agricultural activities. The extremely high PAH concentrations and their ecological and health risks require special attention and strict regulation.

Distribution Characteristics and Source Apportionment of Polycyclic Aromatic Hydrocarbons in Atmospheric Deposition in Areas Adjacent to a Large Petrochemical Enterprise

In order to explore the influence of polycyclic aromatic hydrocarbons (PAHs) emissions by petrochemical enterprises on the surrounding environment, atmospheric deposition samples of the PAHs were collected in the industrial and residential areas adjacent to a petrochemical enterprise from March 2017 to February 2018. Deposition fluxes and the composition of PAHs were studied. The source of PAHs was analyzed by a positive matrix factor (PMF) model. The results showed that the deposition fluxes of Σ15 PAHs ranged from 549 ng·(m2·d)-1 to 18845 ng·(m2·d)-1, with an average of 2712 ng·(m2·d)-1. The flux of Σ15 PAHs in the industrial area was 1.36 times greater than that in the residential area. The deposition fluxes of PAHs in winter and spring were higher than those in summer and autumn. The deposition flux was highest in January in the industrial area and lowest in October in the residential area. Phe, BbF, and Fla were the dominant monomers. There was noticeable difference of monomers between the industrial area and the residential area in summer and autumn. The monomers, such as BbF, BkF, and BgP, in the residential area were higher than those in industrial area, and the proportion of 5, 6 rings was higher, which indicated that traffic contributed more to the residential area; 3 ring PAHs in industrial area had a higher proportion, which pointed out that their main source was petroleum volatilization. Based on the quantitative source analysis, the PAHs in atmospheric deposition were mainly from traffic emissions, petroleum volatilization, and coal combustion. Three sources of PAHs accounted for 45.7%, 18.4%, 35.9%, and 46.3%, 21.4%, and 32.3%, respectively, in the industrial area and the residential area in winter and spring. In summer and autumn, the contribution of traffic sources to the residential area was as high as 65.2%, and the proportion of the petroleum source to the industrial area increased to 35.5%. Due to high-altitude emissions and favorable diffusion conditions, the coal combustion contribution was significantly reduced.

SEASONAL VARIATION OF VOLATILE POLY AROMATIC HYDROCARBONS (PAHS) RELEASED FROM DIFFERENT SOURCES IN SOUTH CAIRO

Understanding the seasonal variations of polycyclic aromatic hydrocarbons (PAHs) concentrations in ambient air in urban/rural or industrial regions is important to the effective control of air pollution in these regions. Based on an approximately a year round dataset (from January to November 2014), a total of 48 atmospheric samples were collected by high volume active air sampler over one year seasonal monitoring in order to assess the variation of PAHs concentrations in different areas through different seasons in south Al Tabbin area. The gaseous and particulate phases of PAHs were extracted and analyzed using GC/MS together. The total air concentrations of 16 USEPA PAHs in the study area ranged from 76.48 ± 19.44 µg/m3 to 26995.86 ± 2835.91 µg/m3, with an average concentration of 7085.08 ± 773.98 µg/m3. Seasonal trends of PAH concentrations were observed with high concentration in winter and low in summer where the average concentration of PAHs in winter were ~1.6 times higher than that in summer. This mainly attributed to meteorological conditions.

Contrasting mixing state of black carbon-containing particles in summer and winter in Beijing

Black carbon (BC) exerts a large impact on climate radiative forcing and public health, and such impacts depend strongly on chemical composition and mixing state. Here a single particle aerosol mass spectrometry (SPA-MS) along with an aerosol chemical speciation monitor was employed to characterize the composition and mixing state of BC-containing particles in summer and winter in Beijing. Approximately 2 million BC-containing particles were chemically analyzed, and the particles were classified into nine and eight different types in summer and winter, respectively, according to mass spectral signatures and composition. The BC-containing particles in summer were dominated by the type of nitrate-related BC (BC-N, 56.7%), while in winter the BC mixed with organic carbon (OC) and sulfate (BCOC-S), and OC and nitrate (BCOC-N) were two dominant types accounting for 44.9% and 16.6%, respectively. The number fractions of BC-N in summer, and BCOC-N and BC-SN in winter increased largely during periods with severe air pollution, suggesting the enhanced secondary formation on BC-containing particles. We also found that the primary emissions of the biomass burning and coal combustion can affect BC mixing state substaintially as indicated by the considerable fraction of BC mixed with levoglucosan and polycyclic aromatic hydrocarbons in winter. Bivariate polar plots and back trajectory analysis indicated that the sulfate-associated BC-containing particles were mostly from regional transport while the nitrate-related type was more from local production. The optical parameter of absorbing Ångström exponents (AAE) of BC was 1.2 and 1.5 in summer and winter, respectively, and the AAE dependence of BC mixing state was also different in the two seasons. While higher fractions of BC-N were observed during lower AAE periods in summer, the variations of dominant OC-related BC-containing particles in winter were fairly stable as a function of AAE.

Interannual Survey on Polycyclic Aromatic Hydrocarbons (PAHs) in Seawater of North Nanao Bay, Ishikawa, Japan, from 2015 to 2018: Sources, Pathways and Ecological Risk Assessment

To improve the understanding of the emission sources and pathways of polycyclic aromatic hydrocarbons (PAHs) in the coastal environments of remote areas, their particulate and dissolved concentrations were analyzed on a monthly basis from 2015 to 2018 in surface waters of Nanao Bay, Japan. The concentration of the targeted 13 species of PAHs on the United States Environmental Protection Agency (USEPA) priority pollutant list in dissolved and particle phases were separately analyzed by high-performance liquid chromatography (HPLC) coupled to a fluorescence detector. Particulate and dissolved PAHs had average concentrations of 0.72 ng∙L−1 and 0.95 ng∙L−1, respectively. While most of the samples were lower than 1 ng∙L−1, abnormally high levels up to 10 ng∙L−1 were observed in the winter of 2017–2018 for particulate PAHs. Based on the isomer ratios of Flu to Flu plus Pyr, it was possible to determine that the pyrogenic loads were greater than the petrogenic loads in all but four out of 86 samples. The predominant environmental pathway for PAHs in winter was determined to be long-range atmospheric transportation fed by the East Asian winter monsoon, while for the summer, local sources were more relevant. By the risk quotients method, it was determined that PAHs in surface seawater presented a very low risk to marine life during the interannual survey.

Polycyclic aromatic hydrocarbons in fresh snow in the city of Harbin in northeast China

Characterizing levels of polycyclic aromatic hydrocarbons (PAHs) in snow and their toxicity is important for understanding snow scavenging of PAHs and associated human health and environmental risks in cold regions. A total of 48 fresh snow samples were collected from six precipitation events during the winter of 2014–2015 at eight (5 urban, 2 suburban and 1 rural) sites across the heavily industrialized and agricultural city of Harbin in northeast China, and were analyzed for the USEPA priority 16 PAHs. Concentrations of the sum of the 16 PAHs from individual snow samples ranged from 0.3 to 2549.6 μg L−1 or nearly four orders of magnitude. The arithmetic mean concentration (±standard deviation) of the 48 samples was 218.1 ± 623.7 μg L−1, and the median value was 10.7 μg L−1. The most abundant PAHs averaged from all the samples were Pyrene (17.1%), followed by Phenanthrene (14.9%), Naphthalene (14.4%), and Fluoranthene (10.2%). The important carcinogenic ∑7PAHs accounted for 58.4% of the total PAHs at locations directly impacted by road traffic. Source apportionment analysis using diagnostic ratios coupled with principal component analysis (PCA) indicated that coal and biomass combustion and vehicle exhausts are the major sources of PAHs in winter. Concentrations of PAHs in snow were significantly correlated with measured levels of PAHs in airborne particulate matter (PM2.5 (R = 0.857, p < 0.05); PM10 (R = 0.831, p < 0.05)), as well as with ambient temperature (R = −0.851, p < 0.05). Almost all (99%) of PAHs measured in the snow were present in particulate phase. The practice of clearing snow by removing it from urban areas and disposing it in suburban and rural areas may create a new pathway of exposure, which needs to be assessed further.

Characteristics of polycyclic aromatic hydrocarbons components in fine particle during heavy polluting phase of each season in urban Beijing

Beijing experienced a period of severe atmospheric particulate pollution from 2015 to 2016. In order to acquire the characteristics of polycyclic aromatic hydrocarbons (PAHs) under heavy polluting status, one year sampling campaign was carried out. We selected PM2.5 samples which had the highest concentrations or suffered serious haze-fog weathers in each month. Through the analysis of data from heavily polluting phase, the mean concentrations of PM2.5 and PAHs in winter (369.63 μg m−3 and 223.60 ng m−3) were obviously higher than that in other seasons. The concentration of Σ16PAHs ranged from 3.22 to 297.01 ng m−3, with a mean value of 77.48 ng m−3. In winter, 4-ring PAH congeners (52.33%) contributed the most in PM2.5, followed by 5-rings (27.05%), 6-rings (11.55%) and 2∼3-rings (9.06%). Summertime measurements showed the highest decline in PAHs concentrations for 3∼5-ring congeners. The diagnostic ratios and PCA analysis manifest that vehicle and combustion emission were major sources and totally occupied 88.57% under heavy polluting stage. Moreover, exponential relationship between LWM/HWM (light/high weight molecule-PAHs) and combustion-derived PAHs, as well as linear relationship between BghiP and ∑PAHs verified that the pollution sources mentioned above affected local atmosphere environment as major sources. The highest total BaP equivalent concentration suggested that toxicity potency under heavy polluting phase was mainly attributed to 5-ring PAHs. Through analysis of carcinogenic-PAHs, potency risk to adults was significantly higher than that to children. BaP, BbF and DahA, which belong to 5-ring congeners, contributed the highest potency carcinogenic risk. BbF in winter, BaP in spring and winter may cause potential risk to local residents.

Comparative major components and health risks of toxic elements and polycyclic aromatic hydrocarbons of PM2.5 in winter and summer in Zhengzhou: Based on three-year data

In this study, 102 PM2.5 samples were collected from an urban site in Zhengzhou during winter and summer from 2012 to 2015. The meteorological impact, chemical characteristics, and health risks of the toxic elements and polycyclic aromatic hydrocarbons (PAHs) in PM2.5 were compared between the two seasons. PM2.5 pollution was relatively severe, especially in winter when meteorological conditions exhibited critical influence on PM2.5 concentration. NO3−, SO42−, and NH4+ were the three most abundant species, accounting for 79% and 90% of total measured water-soluble inorganic ions in winter and summer, respectively. OC, EC, and SOC exhibited relatively high concentrations in winter, and SOC contributed >40% in OC in both seasons. The seasonality of PAHs was associated with PM2.5, with high contribution of four-ringed and five- to six-ringed PAHs in winter and summer, respectively. Fe, Al, Zn, Mg, Mn, and Pb were the most abundant elements in PM2.5 in both seasons. The levels of V, Ag, and As in the winter were almost 8.3, 6.2, and 2.7 times higher than those in summer, respectively. The cancer risk values of As, Ni, and Pb were all higher than 10−6 for adults and children in winter and summer. The non-carcinogenic risks of Pb, As, and Sb for children were beyond the safe level, especially from ingestion. PAHs, BaA, BaP, BbF, and DaA showed potential carcinogenic risk. BaA, BaP, and BbF showed higher cancer risk in winter than in summer for adults and children, whereas DaA showed higher cancer risk in summer than in winter. The calculated non-carcinogenic risk of BaP for children in winter was beyond the safe level. BAP caused high health risk for adults through inhalation but through ingestion and dermal contact for children.

Characteristics and Source Identification of Polycyclic Aromatic Hydrocarbons and n-Alkanes in PM2.5 in Xiamen

ABSTRACT PM2.5 samples were collected to characterize the organic compounds of polycyclic aromatic hydrocarbons (PAHs) and n-alkanes in Xiamen, China, in 2013. The concentrations of PM2.5, PAHs and n-alkanes were 55.53 µg m–3 and 22.14 µg m–3, 15.73 ± 6.25 ng m–3 and 5.65 ± 3.73 ng m–3, and 148.57 ± 36.84 ng m–3 and 97.53 ± 67.46 ng m–3 in winter and summer, respectively, demonstrating higher pollutant levels in wintertime. Benzo[e]pyrene (BeP) was the most abundant PAH, accounting for 32% and 26% of the total quantified PAHs in winter and summer, respectively, followed by coronene (Cor) and phenanthrene (Phe). 5-ring PAHs were the most dominant group, contributing 50.8% and 44.1% to the total quantified PAHs in winter and summer, respectively. Two peaks were exhibited by the homologue distributions of n-alkanes, and the dominant components were enriched in the high molecular weight fraction. Meteorological parameters had a stronger impact on the atmospheric PAH levels in summer than winter, and the most significant parameter was relative humidity (RH), followed by temperature. The diagnostic ratios indicated that PAHs in Xiamen were mainly contributed by petroleum combustion in the two seasons and the concentrations of n-alkanes were mainly influenced by anthropogenic sources. The annual values of the benzo[a]pyrene (BaP) equivalent concentration and incremental lifetime cancer risk (ILCR) were 0.83 ± 0.63 ng m–3 and 7.17 × 10–5 in winter and 1.11 × 10–4 ng m–3 and 3.29 × 10–5 in summer, respectively. The findings illustrated that the overall exposure risk to PM2.5-bound PAHs did not trigger an alert in Xiamen, but higher risks in winter were still shown to exist.

The occurrence and fate of PAHs over multiple years in a wastewater treatment plant of Harbin, Northeast China

The occurrence and fate of polycyclic aromatic hydrocarbons (PAHs) were investigated in wastewater, sludge and surrounding air from the wastewater treatment plant (WWTP) in Harbin, Northeast China. The concentration of total PAHs in the influent, effluent and sludge were 4080ng/L, 864ng/L and 8200ng/gdw, respectively. The total concentration of PAHs showed a trend of first rising, and then decreasing over years in the influent, effluent and sludge, which was in agreement with the usage of coal and oil in Harbin. The level of PAHs was 26–560ng/m3 in air from site 1 (the top of the A/O tank), 62–608ng/m3 in air from site 2 (the vicinity of the WWTP) and 61–686ng/m3 in air from site 3 (the urban district of Harbin). In the influent and effluent, the mean concentration of PAHs followed the sequence of summer>winter>autumn>spring, while the sequence was winter>summer>autumn>spring in sludge and air. Rainfall may be the main reason for higher contamination in summer. Coal fired central heating and indoor dust may be reasons for higher PAHs in winter. The mean removal efficiency of total PAHs was approximately 85% (20% of which was adsorbed onto sludge, and 65% volatilized into air or degraded by biodegradation), and 15% of PAHs were discharged through the effluent. There was approximately 6240kg of PAHs imported into the WWTP every year, 1005kg discharged into the Songhua River through the effluent, and 327kg absorbed onto sludge and the rest was degraded or volatilized into air. PCA was applied to identify the sources of PAHs for both heating and non-heating seasons. In general, coal combustion was the main source of PAHs during the heating season and vehicle exhaust was the main source of PAHs during the non-heating season.

Seasonal variation, spatial distribution and source apportionment for polycyclic aromatic hydrocarbons (PAHs) at nineteen communities in Xi'an, China: The effects of suburban scattered emissions in winter

Seasonal variation and spatial distribution of PM2.5 bound polycyclic aromatic hydrocarbons (PAHs) were investigated at urban residential, commercial area, university, suburban region, and industry in Xi'an, during summer and winter time at 2013. Much higher levels of total PAHs were obtained in winter. Spatial distributions by kriging interpolations principle showed that relative high PAHs were detected in western Xi'an in both summer and winter, with decreasing trends in winter from the old city wall to the 2nd-3rd ring road except for the suburban region and industry. Coefficients of diversity and statistics by SPSS method demonstrated that PAHs in suburban have significant differences (t < 0.05) with those in urban residential in both seasons. The positive Matrix Factorization (PMF) modeling indicated that biomass burning (31.1%) and vehicle emissions (35.9%) were main sources for PAHs in winter and summer in urban, which different with the suburban. The coal combustion was the main source for PAHs in suburban region, which accounted for 46.6% in winter and sharp decreased to 19.2% in summer. Scattered emissions from uncontrolled coal combustion represent an important source of PAHs in suburban in winter and there were about 135 persons in Xi'an will suffer from lung cancer for lifetime exposure at winter levels. Further studies are needed to specify the effluence of the scattered emission in suburban to the city and to develop a strategy for controlling those emissions and lighten possible health effects.

Primary and secondary aerosols in Beijing in winter: sources, variations and processes

Abstract. Winter has the worst air pollution of the year in the megacity of Beijing. Despite extensive winter studies in recent years, our knowledge of the sources, formation mechanisms and evolution of aerosol particles is not complete. Here we have a comprehensive characterization of the sources, variations and processes of submicron aerosols that were measured by an Aerodyne high-resolution aerosol mass spectrometer from 17 December 2013 to 17 January 2014 along with offline filter analysis by gas chromatography/mass spectrometry. Our results suggest that submicron aerosols composition was generally similar across the winter of different years and was mainly composed of organics (60 %), sulfate (15 %) and nitrate (11 %). Positive matrix factorization of high- and unit-mass resolution spectra identified four primary organic aerosol (POA) factors from traffic, cooking, biomass burning (BBOA) and coal combustion (CCOA) emissions as well as two secondary OA (SOA) factors. POA dominated OA, on average accounting for 56 %, with CCOA being the largest contributor (20 %). Both CCOA and BBOA showed distinct polycyclic aromatic hydrocarbons (PAHs) spectral signatures, indicating that PAHs in winter were mainly from coal combustion (66 %) and biomass burning emissions (18 %). BBOA was highly correlated with levoglucosan, a tracer compound for biomass burning (r2 = 0.93), and made a considerable contribution to OA in winter (9 %). An aqueous-phase-processed SOA (aq-OOA) that was strongly correlated with particle liquid water content, sulfate and S-containing ions (e.g. CH2SO2+) was identified. On average aq-OOA contributed 12 % to the total OA and played a dominant role in increasing oxidation degrees of OA at high RH levels (&gt; 50 %). Our results illustrate that aqueous-phase processing can enhance SOA production and oxidation states of OA as well in winter. Further episode analyses highlighted the significant impacts of meteorological parameters on aerosol composition, size distributions, oxidation states of OA and evolutionary processes of secondary aerosols.

Characterization of PM2.5 in Guangzhou, China: uses of organic markers for supporting source apportionment

Organic carbon (OC), elemental carbon (EC), and non-polar organic compounds including n-alkanes (n-C14-n-C40), polycyclic aromatic hydrocarbons (PAHs), phthalate esters (PAEs) and hopanes were quantified in fine particulate (PM2.5), which were collected in urban area of Guangzhou, China in winter and summer in 2012/2013. The pollutants levels were well comparable with the data obtained in previous studies in Pearl River Delta (PRD) region but much lower than most northern Chinese megacities. The contribution of EC to PM2.5 and OC/EC ratio suggest that the pollution sources were relatively consistent in GZ between the two seasons. Benzo[a]pyrene (BaP) was the most abundant PAHs, which were 4.9 and 1.0ng/m3 on average, accounting for 10.7% and 9.1% to the total quantified PAHs in winter and summer, respectively. The total concentrations of PAEs ranged from 289.1 to 2435ng/m3 and from 102.4 to 1437ng/m3, respectively, in winter and summer. Di-n-butyl phthalate (DBP) was the most dominant PAEs. The ambient levels of PAEs could be partly attributed to the widespread uses of the household products, municipal garbage compressing, sewage, and external painting material on the building. Source apportionment for OC with chemical mass balance (CMB) model demonstrated coal combustion, vehicle emission, cooking, and secondary organic compounds (SOC) formation were the four major pollution sources. Both of the indices of n-alkanes and diagnostic PAHs ratios support that anthropogenic sources such as vehicle emission and coal combustion were the significant pollution sources with some extents from epicuticular waxes by terrestrial plants. The ratio of hopanes to EC proved the influences from vehicle emission, and displayed a certain degree of the air aging in the Guangzhou ambient air.

Spatial distribution, sources and ecological risk assessment of polycyclic aromatic hydrocarbons in surface seawater from Yangpu Bay, China

The occurrence of 14 polycyclic aromatic hydrocarbons (PAHs) listed by the United States Environmental Protection Agency was investigated in surface seawater of Yangpu Bay, China in November 2013 (winter) and May 2014 (summer). Seventy-two samples were collected from 12 sampling sites. The total concentrations of PAHs in Yangpu Bay showed obvious variations in different seasons, which varied from 582.8 to 2208.3ngL−1 in winter and 952.4 to 1201.7ngL−1 in summer, respectively. Two-ring PAHs accounted for more than 91.6% of total PAHs in winter, and three-ring PAHs were dominant with 81.6% of total PAHs in summer. Molecular indices analyses indicated that the main source of PAHs in Yangpu Bay could be petrogenic contamination. The ecological risk assessment by Risk quotients (RQNCs and RQMPCs) showed a potential ecological risk of PAHs in Yangpu Bay, indicating a close attention should be paid to pollution of PAHs in the coastal area of Yangpu.

Concentrations, seasonal variations, and outflow of atmospheric polycyclic aromatic hydrocarbons (PAHs) at Ningbo site, Eastern China

Thirty six pairs of gas and particle (PM2.5) atmospheric samples were collected by high-volume samplers from July 2009 to March 2010 at an eastern background site in Ningbo and analyzed for polycyclic aromatic hydrocarbons (PAHs). The total (gas+particle) air concentrations of 16 PAHs ranged from 11.0 to 103ng m−3, with an average of 46.0α23.4ng m−3. Seasonal trends of PAH concentrations were observed with high concentrations in winter and low in summer, mainly due to regional sources and meteorological conditions. The association with other airborne pollutants and diagnostic ratio analysis indicated that PAHs in Eastern China background were predominantly from coal/biomass combustion. Coal combustion controlled atmospheric PAHs in winter, whilst biomass burning became important in summer and autumn. Located at eastern coastal areas, Ningbo site was chosen to estimate the atmospheric outflow of PAHs. Transport fluxes were characterized by elevated values in spring and winter. Southward transport fluxes dominated during the sampling period, presenting the transport from northern to southern China.

Temporal Trends and Spatial Variations of Polycyclic Aromatic Hydrocarbons in Atmospheric PM&lt;sub&gt;10&lt;/sub&gt; of Jinan, China

In order to investigate the distributions and characters of sixteen (U.S. EPA) polycyclic aromatic hydrocarbons (PAHs) in PM10, samples were collected from three districts in Jinan, P.R. China during 2004-2005 and 2008-2009. The total concentrations of 16 PAHs were 33.6-627.3 ng·m-3 in 2004-2005 and 37.4-696.0 ng·m-3 in 2008-2009. Annual variations were slight. A small increase of PAH level presented from 2004-2005 to 2008-2009, while four and five aromatic rings accounted for 70% of all PAHs. An obvious seasonal trend of PAH abundance was observed. The highest concentrations of PAHs were measured in winter. Benzo (k) fluoranthene (BkF, 4-ring) and fluoranthene (FluA, 5-ring) were the most abundant PAHs in winter. Spatial variations of PAHs were obviously impacted by local pollution sources. In non-heating seasons, the district had more industries and traffic presented the most PAHs; in heating seasons, the district that had higher population density appeared more contamination for the domestic heating.