Yu-Chieh Ting  1, Chun-Hung Ku2, Yu-Xuan Zou1, Kai-Hsien Chi3, Jhy-Charm Soo4, Chin-Yu Hsu5,6, Yu-Cheng Chen  This email address is being protected from spambots. You need JavaScript enabled to view it.2,7,8

1 Graduate Institute of Environmental Engineering, National Taiwan University, Taipei, Taiwan
2 National Institute of Environmental Health Sciences, National Health Research Institutes, Miaoli, Taiwan
3 Institute of Environmental and Occupational Health Sciences, National Yang-Ming University, Tainan City, Taiwan
4 Department of Biostatistics, Epidemiology and Environmental Health Sciences, Jiann-Ping Hsu College Public Health, Georgia Southern University, Statesboro, GA 30460, USA
5 Department of Safety, Health and Environmental Engineering, Ming Chi University of Technology, New Taipei City, Taiwan
6 Center for Environmental Sustainability and Human Health, Ming Chi University of Technology, New Taipei City, Taiwan
7 Department of Occupational Safety and Health, China Medical University, Taichung, Taiwan
8 Department of Safety, Health and Environmental Engineering, National United University, Miaoli, Taiwan

Received: April 19, 2023
Revised: August 8, 2023
Accepted: August 19, 2023

 Copyright The Author(s). This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are cited.

Download Citation: ||https://doi.org/10.4209/aaqr.230092  

Cite this article:

Ting, Y.C., Ku, C.H., Zou, Y.X., Chi, K.H., Soo, J.C., Hsu, C.Y., Chen, Y.C. (2023). Characteristics and Source-specific Health Risks of Ambient PM2.5-bound PAHs in an Urban City of Northern Taiwan. Aerosol Air Qual. Res. 23, 230092. https://doi.org/10.4209/aaqr.230092


  • PM2.5-bound PAHs and their source-specific human health risks were evaluated.
  • Seasonal variations of PAHs with a high level in winter were obtained.
  • BghiP, BbF, IND, and CHR were typical markers of urban PAHs.
  • Source-health risk assessment can guide effective mitigation strategies.
  • Traffic emissions mainly contributed to human cancer risks in the city.


Polycyclic aromatic hydrocarbons (PAHs) with highly toxic compounds mainly exist in small-sized particles and can induce considerable human health risks. Studies on PM2.5-bound PAHs and their source-specific human health risks still remain scarce. Daily PM2.5 samples (n = 119) were collected every three days from 2016 to 2017 in Taipei city, Taiwan. Fifteen PAHs in PM2.5 were analyzed via gas chromatography tandem mass spectrometry (GC/MS-MS). We utilized a positive matrix factorization (PMF) model, diagnostic ratios, and potential source contribution function (PSCF) to identify the origins of PM2.5-bound PAHs. The annual concentration of total PAHs (TPAH) was 0.79 ± 0.67 ng m–3 (range = 0.11–3.27 ng m–3). The highest and lowest values of TPAH appeared in winter and autumn with a mean of 1.36 ng m–3 and 0.43 ng m–3, respectively. The contributions of high-molecular-weight PAHs (HMW PAHs) to TPAH were notably higher than those of low-molecular-weight PAHs (LMW PAHs) during the sampling period. Benzo[ghi]perylene (BghiP) accounted for the highest percentage (23.9%) of TPAH among selected congeners. Traffic emissions (31.3%) were identified as the predominant contributor to ambient PM2.5-bound PAHs, followed by industrial emissions (29.2%), evaporated/unburned oil (22.3%), and biomass/coal combustion (17.1%). Apart from the local sources, PSCF-derived results showed that emissions from industrial activities in northeast China and shipping around the Yellow Sea and East China Sea could affect the PAHs in the study area. Traffic emissions were the strongest contributor to human health risk, thus pointing to the significance of control over vehicle exhaust. This study suggests that it is necessary to distinguish the sources of the PM2.5-bound PAHs in order to underpin preventive and mitigative strategies for protecting environmental and public health.

Keywords: PAHs, Seasonal variation, Source identification, Source-specific health risk, Urban


Particulate matter (PM) in the atmosphere has received extensive public and research attention because of its adverse impact on air quality and human health (Anderson et al., 2012; Pope and Dockery, 2006; Rohr and Wyzga, 2012), climate change (Bonasoni et al., 2010; Park et al., 2010; Strawa et al., 2010), and visibility (Watson, 2002) in the last decades. Among suspended particles, fine particles (PM2.5) have come to the forefront as their physical and chemical properties pose a greater threat to air quality, human health, and climate change than those of coarse particles (PM2.5-10) (Pope and Dockery, 2006; Squizzato et al., 2016). PM2.5 is referred to as a human carcinogen (Group 1) by the International Agency for Research on Cancer (IARC) (Loomis et al., 2013).

Polycyclic aromatic hydrocarbons (PAHs) are a large group of organic compounds consisting of two or more benzene rings that can be derived from both natural and anthropogenic sources, such as biomass burning, incomplete combustion, and vehicle emissions (Wang et al., 2013; Lin et al., 2019). PAHs in ambient air exist in the vapor phase and are adsorbed on airborne particulate matter, depending on the atmospheric conditions (e.g., temperature and relative humidity) and the properties of aerosols and individual PAHs (Zhou et al., 2014; Zhang et al., 2017). In general, high-molecular-weight PAHs (HMW PAHs, 5–6 rings) exist in the particulate phase, whereas low-molecular-weight PAHs (LMW PAHs, 2–4 rings) exist in the vapor phase because of their vapor pressures (Wei et al., 2015; Tomaz et al., 2016; Zhang et al., 2017). Previous studies have shown that HMW PAHs are released from biomass burning (Chiu et al., 2011; Pham et al., 2019) and traffic emissions (Guarieiro et al., 2014; Shen et al., 2013), whereas LMW PAHs are emitted from evaporated oil and biomass burning (Liu et al., 2015b; Bragato et al., 2012; Sun et al., 2018).

Globally, PAHs have attracted research interest owing to their wide distribution and adverse effects on human health and the environment (Hong et al., 2015; Mehmood et al., 2020; Pongpiachan et al., 2015). With their different toxicity levels and ambient concentrations, PAHs have been classified as human mutagens and carcinogens by the United States Environmental Protection Agency (U.S. EPA) and World Health Organization (WHO) (WHO, 2000; U.S. EPA, 2017). The European Union (EU) has also recommended ambient air quality standards for benzo[a]pyrene (BaP) (EU, 2005). Given high population densities and heavy traffic flows, exposure to PAHs via inhalation has become an important issue in the urban areas. Studies conducted earlier have demonstrated that urban areas may have an exceptionally high concentration of PM2.5-bound PAHs (He et al., 2014; Yu et al., 2018; Mehmood et al., 2020). PAHs occur in higher concentrations in cold seasons than in warm seasons (Teixeira et al., 2012; Chen et al., 2021). This can be attributable to the meteorological conditions, such as reduced wind speed, lower atmospheric mixing heights, and decreased photochemical oxidation of PAHs due to reduced solar radiation exposure. High PAH concentrations in winter associated with coal combustion for heating and elevated emissions from gasoline vehicles with cold starting and idling at low temperatures were also reported (Wu et al., 2014). The dominant sources of PAHs in the urban areas include traffic emissions and biomass/coal combustion (Callén et al., 2014; Manoli et al., 2016; Chao et al., 2019).

Taipei, the biggest city in Taiwan, has a population of approximately 2.7 million and an extremely high population density (9314 people per km2). With the heavy traffic flow across Taipei, PAH concentrations and characteristics in ambient aerosols have attracted increasing attention in recent decades (Lee et al., 2015; Chen et al., 2018), in particular, with regard to human health risks (Wang et al., 2021; Chuang et al., 2020). Hsu et al. (2019) reported several methods to quantify the impact on air quality and health risk of long-range transport (LRT) in the Taipei city and pointed to coal combustion- and traffic-related emissions as the primary PAH sources. Exposure to air pollution from cooking (APC) is a non-negligible source of PAHs (Yu et al., 2015). Huang et al. (2012) found that exposure to traffic-emitted fine particles and PM2.5-bound PAH could cause DNA damage. Zhao et al. (2011) used the excess lifetime cancer risk (ESCR) to assess inhalation exposure to APC at night markets in Taiwan and estimated that ESCR was above the acceptable risk range of 10−6–10−4 for workers, as suggested by the U.S. EPA. Room et al. (2023) investigated the PM2.5-bound PAHs in an urban area and city tunnel in Taipei, and it indicated that coal-fired power plants and traffic emission were the main sources. In addition, Ngo et al. (2022) found that incineration, fossil fuel and biomass burning were the main contributors of PAHs in Taiwan. Previous studies in Taipei have identified several sources and estimated the human health risks of PAHs from receptor models. However, studies about the physicochemical properties and source-specific health impacts of PM2.5-bound PAHs in Taipei city remain limited.

In this study, a year-round sampling campaign of PM2.5 was conducted in Taipei city. The seasonal variations in PM2.5 and PM2.5-bound PAHs were investigated. Sources of PM2.5-bound PAHs were identified via a receptor model of positive matrix factorization (PMF) and ancillary information regarding the diagnostic ratios of congeners. A potential source contribution function (PSCF) was also performed to determine the regional contributions of PM2.5-bound PAHs sources. The identified sources were further utilized to assess the health risks of PM2.5-bound PAHs. The source-oriented health assessment of PM2.5-bound PAHs is a novel approach that offers valuable insights into developing mitigation strategies for air pollution.


2.1 Description of the Study Area and Sampling

From December 2016 to November 2017, daily PM2.5 samples (24-hour integrated) were gathered every three days at the Air Quality Monitoring Station (AQMS) situated in Guting (25°1′15′′N, 121°31′49′′E), which is located in Taipei city, Taiwan. The sampling site was located in the residential and commercial areas surrounded by the main traffic road, as shown in Fig. 1. A total of 119 samples were collected and analyzed in this study. A sampler (PQ200, BGI Inc., MA, USA) at a flow rate of 16.7 L min1 was used to collect the PM2.5 samples on the 47 mm quartz fiber filters for 24 h in the ambient environment. The total volume of air that passed through the filter for each sample was recorded, and the sampler flow rate for each sample was readjusted via a calibration rotameter (Defender 520, MesaLabs, NJ, USA). The mass of PM2.5 on the filters was weighed via an electronic microbalance (MX5, Mettler-Toledo, Switzerland, ± 0.002 mg). Before and after sampling, the samples were kept in a desiccator shielded from light at a temperature of 23 ± 1°C and relative humidity of 40 ± 5% for 24 h.

Fig. 1. Location of sampling site.Fig. 1. Location of sampling site.

2.2 PAH Analysis

The quartz filters were extracted with 25 mL of a mixture of dichloromethane (DCM) and hexane (2:1) for 15 mins at 100°C via a MARS Xpress microwave digestion instrument. After extraction, an automated evaporation and concentration system (XcelVap, Horizon Technology Inc., Salem, USA) was used to concentrate the extract to about 0.8 mL, and the remaining extract was purified by using solid-phase extraction (ProElutTM Bap extraction cartridge, CA, USA). The extracted solution was then reconstituted to 1 mL with hexane, and 100 µL of the internal standard mixture was added (naphthalene-d8, acenaphthene-d10, phenanthrene-d10, chrysene-d12, perylene-d12). A gas chromatographer (Agilent Technologies 7890 B) coupled with mass spectrometric detection (Agilent Technologies 7000C MS-MS Triple Quad) and multiple reaction monitoring (MRM) modes with a capillary column (Agilent 122-9632 DB-EUPAH) with dimensions of 0.25 mm (internal diameter) × 30 m (length) × 0.25 um (film thickness) was used to analyze PAHs. A constant flow rate (1.2 mL min1) of helium was used as the carrier gas. Gas chromatography tandem mass spectrometry (GC-MS/MS) was used according to the following procedure: the oven temperature was held at 80°C for 1 min, heated to 200°C at a rate of 25°C min1, and elevated to 335°C at a rate of 8°C min1 (hold for 17.325 min). Each compound was positively identified via the retention time in GC-MS/MS in MRM mode. Table S1 lists the optimized MRM transitions with collision energies. The method detection limit (MDL) of all target compounds ranged from 0.63 to 1.19 ng mL1 (Table S1). A mixture of PAH standards was added to the blank filters by using the same analysis protocol to quantify the recovery rate. The recovery rates of the target PAHs ranged from 79.2% to 98.0% (Table S1). Fifteen PAHs, listed as priority pollutants by U.S. EPA, were determined: acenaphthylene (AcPy), acenaphthene (Acp), fluorene (Flu), phenanthrene (PA), anthracene (Ant), fluoranthene (FL), pyrene (Pyr), benzo[a]anthracene (BaA), chrysene (CHR), benzo[b]fluoranthene (BbF), benzo[k]fluoranthene (BkF), benzo[a]pyrene (BaP), indeno[1,2,3-cd]pyrene (IND), dibenzo[a,h]anthracene (DBA), and benzo[g,h,i]perylene (BghiP).

2.3 Source Identification

Positive matrix factorization (PMF) 5.0 model was used to identify and quantify the contributions of PAH sources. Details of the PMF model can be found in the U.S. EPA PMF 5.0 Fundamentals & User Guide (Norris et al., 2014). Briefly, a modified dataset can be regarded as a data matrix X of i × j dimension as Eq. (1):


where i is the number of samples; j is the number of species; p is the number of factors; fkj is the species profile of each source; gik is the amount of mass contributed by each source; and eij represents the residuals. Uncertainty of the PMF model was estimated by using the method detection limit (MDL) and error fraction. Eqs. (2) and (3) were used when the concentrations were lower and higher than MDL, respectively, as follows:  


Potential source contribution function (PSCF) analysis (Polissar et al., 2001; Pongkiatkul and Kim Oanh, 2007) was performed via Zefir, an Igor-based package (Petit et al., 2017), to determine the origin of air pollutants according to Eq. (4). The spatial resolution of each cell in the PSCF results was 0.3° × 0.3° with the 75th percentile threshold when the total number of trajectory endpoints (mij) was calculated. The weighting function was derived from Eq. (5) as follows: 


where nij is the total number of trajectory endpoints in the ijth cell; mij is the total number of trajectory endpoints in the ijth cell related to PAH concentrations above the defined threshold; and wij is an arbitrary weighting function used to reduce uncertainty in PSCF results. The 120-h back trajectories at an altitude of 200 m above sea level were obtained via the HYbrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT, version 4.9) model (Stein et al., 2015) developed by the National Oceanic and Atmospheric Administration Air Resources Laboratory. Global Data Assimilation System (GDAS) data were used for the calculations.

2.4 Health Risk Assessment

The Toxic Equivalent Quantity (TEQ) and Mutagenic Equivalent Quantity (MEQ) values were used to estimate the toxicity and mutagenicity of individual PAHs regulated by U.S. EPA, each of which has a corresponding toxic and mutagenic equivalency factor, respectively. Among PAHs, BaP, a reference compound, is the most suitable indicator to assess the carcinogenic potential of PAHs in the human body through different exposure pathways (Nisbet and LaGoy, 1992). The BaP equivalent concentration (BaPeq) was estimated from Eqs. (6) and (7). The concentration of the target PAH (ng m3) and its toxic and mutagenic equivalence factors were obtained from previous studies in related literature (Nisbet and LaGoy, 1992; Schoeny and Poirier, 1993; Durant et al., 1999), as shown in Tables S5 and S6. 


where Ci is the concentration of the target PAH (ng m–3); TEFi and MEFi are the toxic and mutagenic equivalence factors of the target PAH, respectively; and BaPTEQ and BaPMEQ are BaP equivalencies resulting from the product of the target PAH concentration and its individual TEF or MEF, respectively. The lifetime lung cancer risk (LLCR) associated with inhalation exposure to PAHs was estimated from Eq. (8) (Bari et al., 2011; Collins et al., 1998):


where IURBaP is the inhalation unit risk, defined as 8.7  105 per ng m3 via inhalation exposure (WHO, 2000).


3.1 Mass Concentrations of PM2.5 and PAHs

During the sampling period, the PM2.5 concentration ranged from 2.28 to 40.94 µg m–3 with a mean of 16.56 ± 7.93 µg m–3 (Fig. 2), higher than the annual standard (15 µg m–3) of the Taiwan EPA (MOENV, 2020) and the annual guideline limit (5 µg m–3) of the WHO (WHO, 2022). Because of seasonal variations, the mean PM2.5 concentration was highest in spring (20.15 ± 7.73 µg m3), followed by that in winter (18.73 ± 8.31 µg m–3), summer (13.87 ± 6.60 µg m–3), and autumn (13.72 ± 7.26 µg m–3). The highest concentration of PM2.5 in spring could be attributed to frequent transboundary air pollutants from the northeast monsoon and fewer rainy days in the spring, as compared with other seasons. The reason for the significant difference between the cold and warm seasons was probably due to several factors. For instance, the higher mixing layer in the warm period than in the cold period may have enhanced atmospheric dispersion, thus decreasing ambient PM2.5; the contribution of the long-range transport of the northeast monsoon (from October to April) to ambient aerosol concentration from the coastal cities in China and East Asia to northern Taiwan in the cold season could increase PM2.5 concentration (Hsu et al., 2019; Hung et al., 2019; Luo et al., 2018; Kishcha et al., 2018; Wang et al., 2016c).

Fig. 2. Annual and seasonal average concentrations of the 15 PM2.5-bound PAHs and PM2.5.Fig. 2. Annual and seasonal average concentrations of the 15 PM2.5-bound PAHs and PM2.5.

The annual concentration of the total PAHs (TPAH) ranged from 0.11 to 3.27 ng m–3 with an average of 0.79 ± 0.67 ng m–3, as shown in Table S2. The annual TPAH concentration was significantly lower in the study area than in Guangzhou, China (33.89 ng m–3) (Liu et al., 2015a); Tehran, Iran (12.2 ng m–3) (Taghvaee et al., 2018); Beijing, China (92.62 ng m–3) (Yu et al., 2018); and Islamabad, Pakistan (25.69 ng m–3) (Mehmood et al., 20200) but higher in the study area than in Kanazawa, Japan (0.53 ng m–3) (Kalisa et al., 2019) and Ciudad Real, Spain (0.54 ng m–3 in PM10-bound PAHs) (Lara et al., 2022). In comparison to previous studies on PAHs (3.84 ng m–3) conducted in Taipei (Hsu et al., 2019), this study exhibits a lower mean concentration of total PAHs. This can be attributed to improved air quality and a reduction in the number of observed PAH congeners. The seasonal variations of the annual TPAH concentration exhibited the following pattern: winter (1.36 ng m–3) > spring (0.86 ng m–3) > summer (0.60 ng m–3) > autumn (0.43 ng m–3), similar to those in Islamabad, Pakistan (Mehmood et al., 2020); Shizuoka, Japan (Ohura et al., 2004); and Ontario, Canada (Anastasopoulos et al., 2012). The average concentration of the PM2.5-bound TPAH in winter was approximately two and three times higher than that in summer and autumn, respectively, probably because of the effect of ambient temperature on gas-particle phase partitioning. The higher TPAH concentration in the cold seasons might be due to long-range transport from northeast China, where biomass/coal combustion for heating is prevalent in the cold seasons (Hsu et al., 2019; Lai, 2015), whereas the lower TPAH concentration in the warm seasons could be attributed to the increased volatilization of the PAHs (Chen et al., 2020; Vlachou et al., 2019; Tan et al., 2006).

In the sampling period, the concentrations of PM2.5-bound PAHs reduced in the given order: BghiP > BbF > IND > CHR > FL > Pyr > BaP > BkF > PA > BaA > AcP > DBA > AcPy > Ant > Flu. According to the annual and seasonal proportions of each PAH to TPAH in Fig. S1, BghiP accounted for the highest percentage (16–24%) of TPAH among the four seasons. The average concentrations of BghiP, BbF, IND, and CHR were the predominant PAHs, whereas Flu, Ant, AcPy, and Acp often showed a low average concentration in the four seasons. Previous studies have also reported that BghiP, BbF, IND, and CHR were the dominant PAH species in other urban areas, such as Bangkok, Beijing, and Shanghai (ChooChuay et al., 2020; Chao et al., 2019; Wang et al., 2016a), implying that these PAH species might be originated from the general sources in urban area. The further investigation of sources would be discussed in Section 3.2.

According to their molecular weights, PAHs were classified into the following two groups: low-molecular-weight (LMW) (AcPy, Acp, Flu, PA, and Ant) and high-molecular-weight (HMW) (FL, Pyr, BaA, CHR, BbF, BkF, BaP, DBA, IND, and BghiP), as shown in Table S2. The annual HMW PAH concentration ranged from 0.07 to 3.00 ng m–3 with the highest and lowest mean values of 1.27 ± 0.67 ng m–3 and 0.38 ± 0.18 ng m–3 in winter and autumn, respectively. The annual LMW PAH concentration ranged from 0.03 to 0.27 ng m–3 with the highest and lowest mean values of 0.09 ± 0.07 ng m–3 and 0.04 ± 0.01 ng m–3 in winter and summer, respectively. The mean HMW PAH concentration was higher than the mean LMW PAH over the sampling period, probably owing to the low molecular weight and high volatility of the PM-bound PAHs, resulting in a tendency to exist in the gaseous phase. Both HMW and LMW PAHs showed the highest concentrations in winter, consistent with those in Thessaloniki, Greece (Manoli et al., 2016) and Isfahan, Iran (Soleimani et al., 2022). A significant difference in the HMW PAH concentration was found between winter and autumn, probably due to the influence of meteorological factors on the PM2.5-bound PAHs (Manoli et al., 2016).

According to the number of benzene rings, PAHs can be divided into 3 rings (i.e., AcPy, Acp, Flu, PA, and Ant), 4-rings (i.e., FL, Pyr, BaA, and CHR), 5-rings (i.e., BbF, BkF, BaP, and DBA), and 6-rings (i.e., IND and BghiP). As shown in Fig. 3, the 6-ring PAHs were the largest contributor (34%) to the annual average TPAH concentration, followed by 5- (29%), 4- (28%), and 3-ring PAHs (8%). This pattern was also found in spring, summer, and autumn but not in winter, which might be due to the chemical characteristics of the PAHs. Because the PAHs are semi-volatile organic compounds, temperature has been regarded as a critical regulator of the partitioning of the PAHs into the particle and gas phases (Chetwittayachan et al., 2002), in particular for the 4- and 5-ring PAHs. As shown in Table S2, the mean 4-ring PAH concentration in winter (0.44 ng m–3) was approximately five times that in summer (0.09 ng m–3), while the mean 5-ring PAH concentration in winter (0.40 ng m–3) was over three times that in summer (0.13 ng m–3). However, the average 6-ring PAH concentration in winter (0.38 ng m–3) was only approximately two times that in summer (0.18 ng m–3). Similar seasonal patterns of the PAHs have also been observed in Islamabad and Hsinchu (Mehmood et al., 2020; Yang et al., 2017), which might be due to the high volatility and vapor pressure of the LMW PAHs (Bandowe et al., 2014).

 Fig. 3. Annual and seasonal contributions of the PAHs with different numbers of benzene rings to TPAH concentration.Fig. 3. Annual and seasonal contributions of the PAHs with different numbers of benzene rings to TPAH concentration.

3.2 Identification and Contribution of Sources to PAH

3.2.1 Positive matrix factorization (PMF)

The sources and their contribution to the individual PAHs identified via the PMF 5.0 model during the study period are illustrated in Fig. 4. The following four main sources contributing to TPAH were identified: evaporated/unburned oil (22.3%), industrial emissions (29.2%), traffic emissions (31.3%), and biomass/coal combustion (17.1%).

Fig. 4. Profiles of the four sources (in percentage) identified by the PMF 5.0 model for 15 individual PAHs over the year.Fig. 4. Profiles of the four sources (in percentage) identified by the PMF 5.0 model for 15 individual PAHs over the year.

Factor 1 was identified as evaporated/unburned oil with the high levels of Ant (84%), Acpy (60%), Acp (61%), and Flu (52%). Previous studies have regarded these PAHs as the typical markers for the volatilization of petroleum and crude oil (Wang et al., 2016b; Liu et al., 2015a; Marr et al., 1999). The LMW PAHs, such as Ant, Flu, and PA, appeared to originate from petroleum spills (Hu et al., 2013). As shown in Fig. 5, the proportion of TPAH in factor 1 was notably higher in summer (30.9%) and autumn (44.4%) than in spring (15.5%) and winter (17.4%), which could be attributed to the effect of the high ambient temperature (Tomaz et al., 2016; Van Drooge et al., 2010).

Fig. 5. Box plots of the contributions of the four sources to TPAH concentration in the four seasons, respectively. The boxes enclose the 25th, 50th, and 75th percentiles and the whiskers represent the 5th and 95th percentiles, respectively.Fig. 5. Box plots of the contributions of the four sources to TPAH concentration in the four seasons, respectively. The boxes enclose the 25th, 50th, and 75th percentiles and the whiskers represent the 5th and 95th percentiles, respectively.

Taghvaee et al. (2018) indicated that gas stations could release the LMW PAHs, which could be a major source of evaporated oil in urban areas. In addition, heavy oil used for shipping has been suggested as one of the emission sources of Ant (Sugiyama et al., 2017; Cooper, 2003). AcPy and Acp serve as markers for the volatilization of crude oil or oil-contaminated surface water (Bamford et al., 1999; Marr et al., 1999). Flu and BghiP also act as indicators for oil spills or evaporation (Elzein et al., 2020). Furthermore, Tai and Chang (2022) pointed out that emissions from shipping activities can impact air quality in Taipei.

Factor 2 was attributed to industrial emissions with the relatively high proportions of PA (67%), FL (69%), and Pyr (70%), which might be produced by the coke-making process (Ciaparra et al., 2009). The HMW PAHs, such as CHR (41%), BbF, and BkF, can arise from the sintering process (Ciaparra et al., 2009; Lin et al., 2011). Factor 2 was the highest contributor to TPAH in winter (38.5%), which might be due to the emissions from the local steel and iron industries around northern Taiwan (Chen et al., 2016; Dat et al., 2018) and the long-range transport in the monsoon season (Li et al., 2017; Lai, 2015). This factor appeared to be determined by industrial activities from Hebei, Shandong, and other northeast China provinces and coastal cities and transported to northern Taiwan by the northeast monsoon in the cold seasons (Song et al., 2015; Han et al., 2019b).

Factor 3 was identified as traffic emissions mainly composed of the HMW PAHs, including BbF (31%), BkF (31%), BaP (47%), IND (42%), DBA (74%), and BghiP (48%). This factor contributed to the highest proportion of TPAH (31.3%), as was also reported for Taiwan by previous studies (Hsu et al., 2019; Chen et al., 2016). The HMW PAHs were previously reported to be mainly produced by the high-temperature combustion processes, such as emissions of gasoline-powered vehicles (Duval and Friedlander, 1981; Dachs et al., 2002). In addition, BghiP and IND have been recognized as indicators of vehicle exhaust and gasoline emissions (Miguel et al., 1998; Duval and Friedlander, 1981), while BaP, IND, and BghiP have been shown to be strongly correlated with traffic emissions in East Asia (Chao et al., 2019; Dat et al., 2018). This factor contributed a higher proportion of TPAH in spring (39.0%) and summer (33.3%) than did the other factors in the study period. Traffic emissions were reported as the dominant sources of PM2.5 in northern Taipei (Ho et al., 2018; Liang et al., 2013). Previous studies in Taipei also denoted that vehicular emission was the major source of ambient PM2.5-bound PAHs (Hsu et al., 2019; Room et al., 2023).

Factor 4 was considered biomass/coal combustion with high BaA (78%) and several species of HMW PAHs, such as BkF (32%) and BaP (35%). Ravindra et al. (2008), Caricchia et al. (1999), Mai et al. (2003), and Larsen and Baker (2003) have indicated BbF, CHR, and BaP as the markers of biomass/coal combustion. The contribution of factor 4 to TPAH was higher in winter (18.3%) and spring (18.2%) than in summer (5.1%) and autumn (9.6%), which might be due to the emissions of coal-fired power plants in Linkou or long-range transport of domestic heating emissions in China (Li et al., 2021; Horak et al., 2017). It was also reported that coal combustion was one of the major sources of PM2.5-bound PAHs in the Taipei urban area (Hsu et al., 2019; Room et al., 2023).

3.2.2 Diagnostic ratio

To further distinguish the potential sources of the PAHs, the diagnostic ratios of individual PAHs, such as Ant/Ant+PA, FL/FL+Pyr, BaA/BaA+CHR, and IND/IND+BghiP, were used as indicators for source identification (Gschwend and Hites, 1981; Budzinski et al., 1997; Sicre et al., 1987; Soclo et al., 2000; Yunker et al., 2002), as shown in Fig. 6. The average ratios for the study period are listed in Table S3. The ratio of Ant/Ant+PA indicated a pyrogenic source when > 0.10 and a combustion source when < 0.10. This ratio in this study was greater than 0.10 in all the seasons (0.16, 0.23, 0.40, and 0.14, respectively), indicating that biomass combustion emissions might be one of the main PAH sources. In fact, the PAHs could result from a mixture of combustion and petroleum emissions, as observed in Rome (Finardi et al., 2017), Shanghai (Yang et al., 2021), and Ciudad Real (Lara et al., 2022). The ratio of FL/FL+Pyr pointed to the petroleum source when < 0.40 (Yunker et al., 2002; Ravindra et al., 2006), to diesel and gasoline emissions when between 0.40 and 0.50, and to biomass combustion when > 0.50 (De La Torre-Roche et al., 2009). In this study, this ratio varied between 0.40 and 0.50 in spring (0.46) and summer (0.49), but was above 0.50 in autumn (0.60) and winter (0.52), indicating that biomass burning as well as diesel and gasoline emissions might be the possible sources, as was also found in the urban areas by previous studies (Varea et al., 2011; ChooChuay et al., 2020). The ratio of BaA/BaA+CHR indicated a petroleum source when < 0.20, petroleum combustion (e.g., crude oil and liquid fossil fuel combustions) when between 0.20 and 0.35, and diesel traffic emissions when > 0.35 (Yunker et al., 2002). This ratio in all the four seasons in the present study varied between 0.20 and 0.35 (0.25, 0.24, 0.21, and 0.20, respectively), thus indicating the importance of petroleum combustion emission to the air quality in Taipei. The ratio of IND/IND+BghiP refers to a petrogenic source when < 0.20, to biomass/coal combustions when > 0.50 (Kavouras et al., 2001), and to petroleum combustion emission when between 0.20 and 0.50. In this study, the majority of this ratio in the four seasons varied between 0.20 and 0.50, which verified the significant contribution of petroleum emissions, as was also found in the urban areas by previous studies (Soleimani et al., 2022; Chao et al., 2019). Thus, liquid fossil fuels, diesel emissions, and petroleum combustion were the main sources of the PM2.5-bound PAHs according to the diagnostic ratio results. The contributions of biomass/coal combustion were relatively low but should not be ignored, in particular, in spring (Lin et al., 2014).

Fig. 6. Diagnostic ratios of (a) Ant/Ant+PA, (b) FL/FL+Pyr, (c) BaA/BaA+CHR, and (d) IND/IND+BghiP in the four seasons.Fig. 6. Diagnostic ratios of (a) Ant/Ant+PA, (b) FL/FL+Pyr, (c) BaA/BaA+CHR, and (d) IND/IND+BghiP in the four seasons.

The diagnostic ratios for four sources identified by PMF were shown in Table S3. FL/FL+Pyr for biomass/coal combustion was over 0.5, and BaA/BaA+CHR for biomass/coal combustion was above 0.35. Ind/Ind+BghiP for traffic emission was between 0.2 and 0.5. These results reinforced the reliability of source apportioned by PMF.

3.2.3 PSCF analysis

To better understand the PMF-derived emission sources in Section 3.2.1, PSCF analysis was used to further clarify the regional contributions. Fig. 7 shows the regional contributions of each source to TPAH concentration in the study period. Compared with the other factors, evaporated/unburned oil in Fig. 7(a) exhibited a high PSCF value distributed mainly over the Yellow Sea and East China Sea, which might originate from shipping and harbor activities in the region (Bie et al., 2021; Yu et al., 2021). Evaporated or unburned oil might arise from petroleum spills, as discussed in Section 3.2.1. The origin of industrial emissions in Fig. 7(b) was concentrated in northeast China, a highly industrialized region (Zhou and Yang, 2016; Song et al., 2015). The contributor to TPAH in this area could be transportation from Hebei, Shandong, and other northeast China provinces and coastal cities (Dat et al., 2018; Han et al., 2019b), as was discussed in Section 3.2.1. Fig. 7(c) shows that the distribution of traffic emissions was more divergent than that of the other factors and was mostly from local and coastal urban cities near northern Taiwan, such as Taipei, Hangzhou, Shanghai, and Nanjing. Fig. 7(d) shows that northeast China most contributed to biomass/coal combustion, as was also indicated in previous studies (Zhang et al., 2007; Shen et al., 2013).

Fig. 7. Annual PSCF values and spatial distributions for (a) evaporated/unburned oil, (b) industrial emission, (c) traffic emission, and (d) biomass/coal combustion. The green star marks the location of the sampling area.Fig. 7. Annual PSCF values and spatial distributions for (a) evaporated/unburned oil, (b) industrial emission, (c) traffic emission, and (d) biomass/coal combustion. The green star marks the location of the sampling area.

Emissions of industrial activities and biomass/coal combustion were higher from the northeastern and coastal cities of China than from the local area. However, traffic emissions as the highest contributor originated from the local area. To further distinguish the contributions of different vehicles, an emission inventory should be established in the future. Fig. S3 illustrates the distribution of industrial emissions during the cold season (Figs. S3(a) and S3(d)), primarily concentrated around coastal and eastern cities in China. Conversely, in the warm season (Figs. S3(b) and S3(c)), dominant sources were in proximity to Taiwan, signifying a contribution of local industrial emissions. On the other hand, traffic emissions were consistently centered around northern Taiwan throughout all four seasons, suggesting that local vehicular emissions play a significant role in this source.

3.3 Health Risk Assessment

To assess the potential hazards of the PAHs for human health, the TEQ, MEQ, and LLCR values of the PAHs were evaluated, as shown in Table S4. The values of BaPTEQ and BaPMEQ ranged from 0.02 to 0.45 ng m–3 and 0.02 to 0.50 ng m–3 with an annual average of 0.09 ng m–3 and 0.16 ng m–3, respectively. The BaPTEQ and BaPMEQ values in this study were notably lower than the annual target value of 1 ng m–3 recommended by the EU and those in Thessaloniki, Greece (Manoli et al., 2016); Beijing, China (Yu et al., 2018); and Tak, Thailand (Janta et al., 2020). However, the mean BaPMEQ concentration in this study exceeded the annual reference level of the WHO (0.12 ng m–3). Throughout the sampling periods, a PM2.5 pollution episode (PM2.5 > 35 µg m–3) occurred, during which the BaPTEQ value was nearly three times higher than the annual average. This increase was attributed to a heightened contribution from traffic emissions. The seasonal variations of BaPTEQ and BaPMEQ were consistent with those of the TPAH concentration and higher in winter (0.15 and 0.25, respectively) and lower in autumn (0.04 and 0.08, respectively). Although the mean annual LLCR value (1.0  105) was lower in the study area than in other urban studies (Yu et al., 2018; Soleimani et al., 2022), it remains essential to quantify the source-specific cancer risks for developing effective mitigation strategies in the future.

As shown in Table S5, BaP was the dominant contributor among the PAHs, responsible for 53.63% of the total BaPTEQ level in the four seasons, consistent with the results of previous studies (Gao et al., 2015; Yu et al., 2018). In addition, BbF, BaP, IND, and DBA contributed 11.58%, 10.71%, and 13.67%, respectively, to the total BaPTEQ concentration. The sum of these HMW PAHs amounted to more than 99% of the total BaPTEQ value, similar to particulate PAHs in the urban areas reported by previous studies (Teixeira et al., 2012; Chen et al., 2021). The HMW PAHs, in particular, BaP, a reliable tracer of the toxic PAHs, exhibited higher TEF values and concentrations than did the LMW PAHs (Belis et al., 2011). The BaPMEQ value of the different species, as shown in Table S6, was mainly dominated by BaP (31.75%), BghiP (22.14%), DBA (20.16%), and BbF (19.09%).

There was no significant difference in the individual PAHs among the seasons; however, differences in the sources of the pollutants were detected. Based on the sources identified in Section 3.2.1, the HMW PAHs mainly originated from traffic emissions and biomass/coal combustion, thus pointing to them as the main contributors to human health risks. In addition, the sources contributing to the annual and seasonal BaPTEQ and BaPMEQ values, as shown in Figs. 8 and S2, respectively, demonstrated that traffic emissions and biomass/coal combustion were the dominant contributors throughout the year. Previous studies in urban areas have shown consistent results, exhibiting the significant adverse effects of these two sources on human health (Taghvaee et al., 2018; Han et al., 2019a; Zhang et al., 2019). From the perspective of the seasonal variations, the contributions of traffic emission and biomass/coal combustion exhibited a significant difference between the cold and warm seasons, whereas those of evaporated/unburned oil did not show a significant difference. Not only could these source-specific health risk results be used to quantify the relationship between the sources and their impacts on human health, but they might facilitate in predicting human health risk in different areas based on the source profiles.

Fig. 8. (a) The annual concentrations of the individual PAHs contributing to BaPTEQ, and (b) the annual and seasonal contributions of BaPTEQ and lifetime lung cancer risk (LLCR) according to the four main sources.Fig. 8. (a) The annual concentrations of the individual PAHs contributing to BaPTEQ, and (b) the annual and seasonal contributions of BaPTEQ and lifetime lung cancer risk (LLCR) according to the four main sources.


The annual average concentrations of PM2.5 and TPAH in Taipei city were 16.56 ± 7.93 µg m–3 and 0.79 ± 0.67 ng m–3, respectively. Both PM2.5 and TPAH concentrations showed the same seasonal variation, with higher values noted in the cold season and lower values in the warm season. A significant difference between the cold and warm seasons indicated that the seasonally varying emission sources of PM2.5 and TPAH concentrations need to be further studied. Overall, the mean concentration of the HMW PAHs was notably higher than that of the LMW PAHs both annually and seasonally. Benzo[ghi]perylene (BghiP) accounted for the highest percentage of TPAH among all the HMW PAHs in all the four seasons. The traffic emission was estimated to contribute approximately 31.3% to the annual TPAH concentration, indicating the importance of controls over the traffic-related sources. Diagnostic analysis also showed that petroleum and fuel combustions were the major sources of the PM-bound PAHs. Apart from the local sources, the PAHs appeared to be partially controlled by the long-range transport of emissions from industrial activities in northeast China and shipping around the Yellow Sea and East China Sea. Unlike previous studies in Taipei urban area, we concluded traffic emissions were the dominant contributors to higher cancer risks compared to the other three sources through the assessment of source-oriented health risks. The seasonally varying contributions of traffic emissions and biomass/coal combustion in turn created a significant difference in associated health risks and might be driven by the monsoon-induced long-range transport. The sources of TPAH showed a significant seasonal difference, which altered human health risks and impacts. Thus, traffic emissions and biomass/coal combustion should be well controlled, in particular, during the cold seasons. This study provides insight into effective mitigation strategies for the PM2.5-bound PAHs in the future. In addition, these results can be utilized in health risk assessments through source profiles in other regions.


The authors gratefully acknowledge the funding received from the National Institutes of Environmental Health Sciences and National Health Research Institutes of Taiwan (grant no. EM-107-SP-02 and EM-112-PP-07).


  1. Anastasopoulos, A.T., Wheeler, A.J., Karman, D., Kulka, R.H. (2012). Intraurban concentrations, spatial variability and correlation of ambient polycyclic aromatic hydrocarbons (PAH) and PM2.5. Atmos. Environ. 59, 272–283. https://doi.org/10.1016/j.atmosenv.2012.05.004

  2. Anderson, J.O., Thundiyil, J.G., Stolbach, A. (2012). Clearing the air: a review of the effects of particulate matter air pollution on human health. J. Med. Toxicol. 8, 166–175. https://doi.org/​10.1007/s13181-011-0203-1

  3. Bamford, H.A., Offenberg, J.H., Larsen, R.K., Ko, F.C., Baker, J.E. (1999). Diffusive exchange of polycyclic aromatic hydrocarbons across the air- water interface of the Patapsco River, an urbanized subestuary of the Chesapeake Bay. Environ. Sci. Technol. 33, 2138–2144. https://doi.org/10.1021/es981324e

  4. Bandowe, B.A.M., Meusel, H., Huang, R.J., Ho, K., Cao, J., Hoffmann, T., Wilcke, W. (2014). PM2.5-bound oxygenated PAHs, nitro-PAHs and parent-PAHs from the atmosphere of a Chinese megacity: Seasonal variation, sources and cancer risk assessment. Sci. Total Environ. 473–474. 77–87. https://doi.org/10.1016/j.scitotenv.2013.11.108

  5. Bari, M.A., Baumbach, G., Kuch, B., Scheffknecht, G. (2011). Air pollution in residential areas from wood-fired heating. Aerosol Air Qual. Res. 11, 749–757. https://doi.org/10.4209/aaqr.2010.09.​0079

  6. Belis, C.A., Cancelinha, J., Duane, M., Forcina, V., Pedroni, V., Passarella, R., Tanet, G., Douglas, K., Piazzalunga, A., Bolzacchini, E., Sangiorgi, G., Perrone, M.G., Ferrero, L., Fermo, P., Larsen, B.R. (2011). Sources for PM air pollution in the Po Plain, Italy: I. Critical comparison of methods for estimating biomass burning contributions to benzo(a)pyrene. Atmos. Environ. 45, 7266–7275. https://doi.org/10.1016/j.atmosenv.2011.08.061

  7. Bie, S., Yang, L., Zhang, Y., Huang, Q., Li, J., Zhao, T., Zhang, X., Wang, P., Wang, W. (2021). Source appointment of PM2.5 in Qingdao Port, East of China. Sci. Total Environ. 755, 142456. https://doi.org/10.1016/j.scitotenv.2020.142456

  8. Bonasoni, P., Laj, P., Marinoni, A., Sprenger, M., Angelini, F., Arduini, J., Bonafè, U., Calzolari, F., Colombo, T., Decesari, S., Di Biagio, C., Di Sarra, A.G., Evangelisti, F., Duchi, R., Facchini, Mc., Fuzzi, S., Gobbi, G.P., Maione, M., Panday, A., Roccato, F., et al. (2010). Atmospheric Brown Clouds in the Himalayas: first two years of continuous observations at the Nepal Climate Observatory-Pyramid (5079 m). Atmos. Chem. Phys. 10, 7515–7531. https://doi.org/10.5194/​acp-10-7515-2010

  9. Bragato, M., Joshi, K., Carlson, J.B., Tenório, J.A.S., Levendis, Y.A. (2012). Combustion of coal, bagasse and blends thereof: Part II: Speciation of PAH emissions. Fuel 96, 51–58. https://doi.org/​10.1016/j.fuel.2011.11.069

  10. Budzinski, H., Jones, I., Bellocq, J., Piérard, C., Garrigues, P. (1997). Evaluation of sediment contamination by polycyclic aromatic hydrocarbons in the Gironde estuary. Mar. Chem. 58, 85–97  https://doi.org/10.1016/S0304-4203(97)00028-5

  11. Callén, M.S., Iturmendi, A., López, J.M., Mastral, A.M. (2014). Source apportionment of the carcinogenic potential of polycyclic aromatic hydrocarbons (PAH) associated to airborne PM10 by a PMF model. Environ. Sci. Pollut. Res. 21, 2064–2076. https://doi.org/10.1007/s11356-013-2116-9

  12. Caricchia, A.M., Chiavarini, S., Pezza, M. (1999). Polycyclic aromatic hydrocarbons in the urban atmospheric particulate matter in the city of Naples (Italy). Atmos. Environ. 33, 3731–3738. https://doi.org/10.1016/S1352-2310(99)00199-5

  13. Chao, S., Liu, J., Chen, Y., Cao, H., Zhang, A. (2019). Implications of seasonal control of PM2.5-bound PAHs: An integrated approach for source apportionment, source region identification and health risk assessment. Environ. Pollut. 247, 685–695. https://doi.org/10.1016/j.envpol.2018.12.074

  14. Chen, S.Y., Chu, D.C., Lee, J.H., Yang, Y.R., Chan, C.C. (2018). Traffic-related air pollution associated with chronic kidney disease among elderly residents in Taipei City. Environ. Pollut. 234, 838–845. https://doi.org/10.1016/j.envpol.2017.11.084

  15. Chen, W.H., Hsieh, M.T., You, J.Y., Quadir, A., Lee, C.L. (2021). Temporal and vertical variations of polycyclic aromatic hydrocarbon at low elevations in an industrial city of southern Taiwan. Sci. Rep. 11, 3453. https://doi.org/10.1038/s41598-021-83155-7

  16. Chen, Y.C., Chiang, H.C., Hsu, C.Y., Yang, T.T., Lin, T.Y., Chen, M.J., Chen, N.T., Wu, Y.S. (2016). Ambient PM2.5-bound polycyclic aromatic hydrocarbons (PAHs) in Changhua County, central Taiwan: Seasonal variation, source apportionment and cancer risk assessment. Environ. Pollut. 218, 372–382. https://doi.org/10.1016/j.envpol.2016.07.016

  17. Chen, Z., Chen, D., Zhao, C., Kwan, M., Cai, J., Zhuang, Y., Zhao, B., Wang, X., Chen, B., Yang, J., Li, R., He, B., Gao, B., Wang, K., Xu, B. (2020). Influence of meteorological conditions on PM2.5 concentrations across China: A review of methodology and mechanism. Environ. Int. 139, 105558. https://doi.org/10.1016/j.envint.2020.105558

  18. Chetwittayachan, T., Shimazaki, D., Yamamoto, K. (2002). A comparison of temporal variation of particle-bound polycyclic aromatic hydrocarbons (pPAHs) concentration in different urban environments: Tokyo, Japan, and Bangkok, Thailand. Atmos. Environ. 36, 2027–2037. https://doi.org/10.1016/S1352-2310(02)00099-7

  19. Chiu, J.C., Shen, Y.H., Li, H.W., Chang, S.S., Wang, L.C., Chang-Chien, G.P. (2011). Effect of biomass open burning on particulate matter and polycyclic aromatic hydrocarbon concentration levels and PAH dry deposition in ambient air. J. Environ. Sci. Health A 46, 188–197. https://doi.org/​10.1080/10934529.2011.532438

  20. ChooChuay, C., Pongpiachan, S., Tipmanee, D., Suttinun, O., Deelaman, W., Wang, Q., Xing, L., Li, G., Han, Y., Palakun, J., Cao, J. (2020). Impacts of PM2.5 sources on variations in particulate chemical compounds in ambient air of Bangkok, Thailand. Atmos. Pollut. Res. 11, 1657–1667. https://doi.org/10.1016/j.apr.2020.06.030

  21. Chuang, K.J., Lin, L.Y., Ho, K.F., Su, C.T. (2020). Traffic-related PM2.5 exposure and its cardiovascular effects among healthy commuters in Taipei, Taiwan. Atmos. Environ.: X 7, 100084. https://doi.org/10.1016/j.aeaoa.2020.100084

  22. Ciaparra, D., Aries, E., Booth, M.J., Anderson, D.R., Almeida, S.M., Harrad, S. (2009). Characterisation of volatile organic compounds and polycyclic aromatic hydrocarbons in the ambient air of steelworks. Atmos. Environ. 43, 2070–2079. https://doi.org/10.1016/j.atmosenv.2008.09.078

  23. Collins, J.F., Brown, J.P., Alexeeff, G.V., Salmon, A.G. (1998). Potency equivalency factors for some polycyclic aromatic hydrocarbons and polycyclic aromatic hydrocarbon derivatives. Regul. Toxicol. Pharmacol. 28, 45–54. https://doi.org/10.1006/rtph.1998.1235

  24. Cooper, D.A. (2003). Exhaust emissions from ships at berth. Atmos. Environ. 37, 3817–3830. https://doi.org/10.1016/S1352-2310(03)00446-1

  25. Dachs, J., Glenn, T.R., Gigliotti, C.L., Brunciak, P., Totten, L.A., Nelson, E.D., Franz, T.P., Eisenreich, S.J. (2002). Processes driving the short-term variability of polycyclic aromatic hydrocarbons in the Baltimore and northern Chesapeake Bay atmosphere, USA. Atmos. Environ. 36, 2281–2295. https://doi.org/10.1016/S1352-2310(02)00236-4

  26. Dat, N.D., Lyu, J.M., Chang, M.B. (2018). Variation of atmospheric PAHs in Northern Taiwan during winter and summer seasons. Aerosol Air Qual. Res. 18, 1019–1031. https://doi.org/10.4209/​aaqr.2018.01.0038

  27. De La Torre-Roche, R.J., Lee, W.Y., Campos-Díaz, S.I. (2009). Soil-borne polycyclic aromatic hydrocarbons in El Paso, Texas: Analysis of a potential problem in the United States/Mexico border region. J. Hazard. Mater. 163, 946–958. https://doi.org/10.1016/j.jhazmat.2008.07.089

  28. Durant, J.L., Lafleur, A.L., Busby, W.F., Donhoffner, L.L., Penman, B.W., Crespi, C.L. (1999). Mutagenicity of C24H14 PAH in human cells expressing CYP1A1. Mutat. Res. Genet. Toxicol. Environ. Mutagen. 446, 1–14. https://doi.org/10.1016/S1383-5718(99)00135-7

  29. Duval, M.M., Friedlander, S.K. (1981). Source resolution of polycyclic aromatic hydrocarbons in the Los Angeles atmosphere: application of a chemical species balance method with first order chemical decay. Final report Jan-Dec 80. 

  30. Elzein, A., Stewart, G.J., Swift, S.J., Nelson, B.S., Crilley, L.R., Alam, M.S., Reyes-Villegas, E., Gadi, R., Harrison, R.M., Hamilton, J.F., Lewis, A.C. (2020). A comparison of PM2.5-bound polycyclic aromatic hydrocarbons in summer Beijing (China) and Delhi (India). Atmos. Chem. Phys. 20, 14303–14319. https://doi.org/10.5194/acp-20-14303-2020

  31. European Union (EU) (2005). Directive 2004/107/EC of the European Parliament and of the Council of 15 December 2004 relating to arsenic, cadmium, mercury, nickel and polycyclic aromatic hydrocarbons in ambient air. Official Journal of the European Communities, OJ L 23, 26.1.2005, pp. 3–16. 

  32. Finardi, S., Radice, P., Cecinato, A., Gariazzo, C., Gherardi, M., Romagnoli, P. (2017). Seasonal variation of PAHs concentration and source attribution through diagnostic ratios analysis. Urban Clim. 22, 19–34. https://doi.org/10.1016/j.uclim.2015.12.001

  33. Gao, B., Wang, X.M., Zhao, X.Y., Ding, X., Fu, X.X., Zhang, Y.L., He, Q.F., Zhang, Z., Liu, T.Y., Huang, Z.Z., Chen, L.G., Peng, Y., Guo, H. (2015). Source apportionment of atmospheric PAHs and their toxicity using PMF: Impact of gas/particle partitioning. Atmos. Environ. 103, 114–120. https://doi.org/10.1016/j.atmosenv.2014.12.006

  34. Gschwend, P.M., Hites, R.A. (1981). Fluxes of polycyclic aromatic hydrocarbons to marine and lacustrine sediments in the northeastern United States. Geochim. Cosmochim. Acta 45, 2359–2367. https://doi.org/10.1016/0016-7037(81)90089-2

  35. Guarieiro, A.L.N., Santos, J.V.D.S., Eiguren-Fernandez, A., Torres, E.A., Da Rocha, G.O., De Andrade, J.B. (2014). Redox activity and PAH content in size-classified nanoparticles emitted by a diesel engine fuelled with biodiesel and diesel blends. Fuel 116, 490–497. https://doi.org/​10.1016/j.fuel.2013.08.029

  36. Han, B., You, Y., Liu, Y., Xu, J., Zhou, J., Zhang, J., Niu, C., Zhang, N., He, F., Ding, X., Bai, Z. (2019a). Inhalation cancer risk estimation of source-specific personal exposure for particulate matter–bound polycyclic aromatic hydrocarbons based on positive matrix factorization. Environ. Sci. Pollut. Res. 26, 10230–10239. https://doi.org/10.1007/s11356-019-04198-y

  37. Han, J., Liang, Y., Zhao, B., Wang, Y., Xing, F., Qin, L. (2019b). Polycyclic aromatic hydrocarbon (PAHs) geographical distribution in China and their source, risk assessment analysis. Environ. Pollut. 251, 312–327. https://doi.org/10.1016/j.envpol.2019.05.022

  38. He, J., Fan, S., Meng, Q., Sun, Y., Zhang, J., Zu, F. (2014). Polycyclic aromatic hydrocarbons (PAHs) associated with fine particulate matters in Nanjing, China: Distributions, sources and meteorological influences. Atmos. Environ. 89, 207–215. https://doi.org/10.1016/j.atmosenv.2014.02.042

  39. Ho, W.Y., Tseng, K.H., Liou, M.L., Chan, C.C., Wang, C. (2018). Application of positive matrix factorization in the identification of the sources of PM2.5 in Taipei city. Int. J. Environ. Res. Public Health 15, 1305. https://doi.org/10.3390/ijerph15071305

  40. Hong, Y., Chen, J., Zhang, F., Zhang, H., Xu, L., Yin, L., Chen, Y. (2015). Effects of urbanization on gaseous and particulate polycyclic aromatic hydrocarbons and polychlorinated biphenyls in a coastal city, China: levels, sources, and health risks. Environ. Sci. Pollut. Res. 22, 14919–14931. https://doi.org/10.1007/s11356-015-4616-2

  41. Horak, J., Kubonova, L., Krpec, K., Hopan, F., Kubesa, P., Motyka, O., Laciok, V., Dej, M., Ochodek, T., Placha, D. (2017). PAH emissions from old and new types of domestic hot water boilers. Environ. Pollut. 225, 31–39. https://doi.org/10.1016/j.envpol.2017.03.034

  42. Hsu, C.Y., Chiang, H.C., Chen, M.J., Yang, T.T., Wu, Y.S., Chen, Y.C. (2019). Impacts of hazardous metals and PAHs in fine and coarse particles with long-range transports in Taipei City. Environ. Pollut. 250, 934–943. https://doi.org/10.1016/j.envpol.2019.04.038

  43. Hu, Y., Wen, J., Wang, D., Du, X., Li, Y. (2013). An interval dynamic multimedia fugacity (IDMF) model for environmental fate of PAHs and their source apportionment in a typical oilfield, China. Chem Ecol. 29, 476–488. https://doi.org/10.1080/02757540.2013.769968

  44. Huang, H.B., Lai, C.H., Chen, G.W., Lin, Y.Y., Jaakkola, J.J.K., Liou, S.H., Wang, S.L. (2012). Traffic-related air pollution and DNA damage: a longitudinal study in Taiwanese traffic conductors. PLoS One 7, e37412. https://doi.org/10.1371/journal.pone.0037412

  45. Hung, W.T., Lu, C.H., Wang, S.H., Chen, S.P., Tsai, F., Chou, C.C.K. (2019). Investigation of long-range transported PM2.5 events over Northern Taiwan during 2005–2015 winter seasons. Atmos. Environ. 217, 116920. https://doi.org/10.1016/j.atmosenv.2019.116920

  46. Janta, R., Sekiguchi, K., Yamaguchi, R., Sopajaree, K., Pongpiachan, S., Chetiyanukornkul, T. (2020). Ambient PM2.5, polycyclic aromatic hydrocarbons and biomass burning tracer in Mae Sot District, western Thailand. Atmos. Pollut. Res. 11, 27–39. https://doi.org/10.1016/j.apr.2019.​09.003

  47. Kalisa, E., Nagato, E., Bizuru, E., Lee, K., Tang, N., Pointing, S., Hayakawa, K., Archer, S., Lacap-Bugler, D. (2019). Pollution characteristics and risk assessment of ambient PM2.5-bound PAHs and NPAHs in typical Japanese and New Zealand cities and rural sites. Atmos. Pollut. Res. 10, 1396–1403. https://doi.org/10.1016/j.apr.2019.03.009

  48. Kavouras, I.G., Koutrakis, P., Tsapakis, M., Lagoudaki, E., Stephanou, E.G., Von Baer, D., Oyola, P. (2001). Source apportionment of urban particulate aliphatic and polynuclear aromatic hydrocarbons (PAHs) using multivariate methods. Environ. Sci. Technol. 35, 2288–2294. https://doi.org/10.1021/es001540z

  49. Kishcha, P., Wang, S.H., Lin, N.H., da Silva, A., Lin, T.H., Lin, P.H., Liu, G.R., Starobinets, B., Alpert, P. (2018). Differentiating between local and remote pollution over Taiwan. Aerosol Air Qual. Res. 18, 1788–1798. https://doi.org/10.4209/aaqr.2017.10.0378

  50. Lai, L.W. (2015). Fine particulate matter events associated with synoptic weather patterns, long-range transport paths and mixing height in the Taipei Basin, Taiwan. Atmos. Environ. 113, 50–62. https://doi.org/10.1016/j.atmosenv.2015.04.052

  51. Lara, S., Villanueva, F., Martín, P., Salgado, S., Moreno, A., Sánchez-Verdú, P. (2022). Investigation of PAHs, nitrated PAHs and oxygenated PAHs in PM10 urban aerosols. A comprehensive data analysis. Chemosphere 294, 133745. https://doi.org/10.1016/j.chemosphere.2022.133745

  52. Larsen, R.K., Baker, J.E. (2003). Source apportionment of polycyclic aromatic hydrocarbons in the urban atmosphere:  a comparison of three methods. Environ. Sci. Technol. 37, 1873–1881. https://doi.org/10.1021/es0206184

  53. Lee, J.H., Wu, C.F., Hoek, G., de Hoogh, K., Beelen, R., Brunekreef, B., Chan, C.C. (2015). LUR models for particulate matters in the Taipei metropolis with high densities of roads and strong activities of industry, commerce and construction. Sci. Total Environ. 514, 178–184. https://doi.org/10.1016/j.scitotenv.2015.01.091

  54. Li, F., Gu, J., Xin, J., Schnelle-Kreis, J., Wang, Y., Liu, Z., Shen, R., Michalke, B., Abbaszade, G., Zimmermann, R. (2021). Characteristics of chemical profile, sources and PAH toxicity of PM2.5 in Beijing in autumn-winter transit season with regard to domestic heating, pollution control measures and meteorology. Chemosphere 276, 130143. https://doi.org/10.1016/j.chemosp​here.2021.130143

  55. Li, T.C., Yuan, C.S., Huang, H.C., Lee, C.L., Wu, S.P., Tong, C. (2017). Clustered long-range transport routes and potential sources of PM2.5 and their chemical characteristics around the Taiwan Strait. Atmos. Environ. 148, 152–166. https://doi.org/10.1016/j.atmosenv.2016.10.010

  56. Liang, C.S., Yu, T.Y., Chang, Y.Y., Syu, J.Y., Lin, W.Y. (2013). Source apportionment of PM2.5 particle composition and submicrometer size distribution during an Asian dust storm and non-dust storm in Taipei. Aerosol Air Qual. Res. 13, 545–554. https://doi.org/10.4209/aaqr.2012.06.​0161

  57. Lin, C.Y., Zhao, C., Liu, X., Lin, N.H., Chen, W.N. (2014). Modelling of long-range transport of Southeast Asia biomass-burning aerosols to Taiwan and their radiative forcings over East Asia. Tellus B 66, 23733. https://doi.org/10.3402/tellusb.v66.23733

  58. Lin, T., Hu, L., Guo, Z., Qin, Y., Yang, Z., Zhang, G., Zheng, M. (2011). Sources of polycyclic aromatic hydrocarbons to sediments of the Bohai and Yellow Seas in East Asia. J. Geophys. Res. 116, D23305. https://doi.org/10.1029/2011JD015722

  59. Lin, Y.C., Li, Y.C., Amesho, K.T.T., Chou, F.C., Cheng, P.C. (2019). Characterization and quantification of PM2.5 emissions and PAHs concentration in PM2.5 from the exhausts of diesel vehicles with various accumulated mileages. Sci. Total Environ. 660, 188–198. https://doi.org/10.1016/j.​scitotenv.2019.01.007

  60. Liu, J., Man, R., Ma, S., Li, J., Wu, Q., Peng, J. (2015a). Atmospheric levels and health risk of polycyclic aromatic hydrocarbons (PAHs) bound to PM2.5 in Guangzhou, China. Mar. Pollut. Bull. 100, 134–143. https://doi.org/10.1016/j.marpolbul.2015.09.014

  61. Liu, Y., Wang, S., Lohmann, R., Yu, N., Zhang, C., Gao, Y., Zhao, J., Ma, L. (2015b). Source apportionment of gaseous and particulate PAHs from traffic emission using tunnel measurements in Shanghai, China. Atmos. Environ. 107, 129–136. https://doi.org/10.1016/j.atmosenv.2015.02.041

  62. Loomis, D., Grosse, Y., Lauby-Secretan, B., Ghissassi, F.E., Bouvard, V., Benbrahim-Tallaa, L., Guha, N., Baan, R., Mattock, H., Straif, K. (2013). The carcinogenicity of outdoor air pollution. Lancet Oncol. 14, 1262–1263. https://doi.org/10.1016/S1470-2045(13)70487-X

  63. Luo, M., Hou, X., Gu, Y., Lau, N.C., Yim, S.H.L. (2018). Trans-boundary air pollution in a city under various atmospheric conditions. Sci. Total Environ. 618, 132–141. https://doi.org/10.1016/j.​scitotenv.2017.11.001

  64. Mai, B., Qi, S., Zeng, E.Y., Yang, Q., Zhang, G., Fu, J., Sheng, G., Peng, P., Wang, Z. (2003). Distribution of polycyclic aromatic hydrocarbons in the coastal region off Macao, China: assessment of input sources and transport pathways using compositional analysis. Environ. Sci. Technol. 37, 4855–4863. https://doi.org/10.1021/es034514k

  65. Manoli, E., Kouras, A., Karagkiozidou, O., Argyropoulos, G., Voutsa, D., Samara, C. (2016). Polycyclic aromatic hydrocarbons (PAHs) at traffic and urban background sites of northern Greece: source apportionment of ambient PAH levels and PAH-induced lung cancer risk. Environ. Sci. Pollut. Res. 23, 3556–3568. https://doi.org/10.1007/s11356-015-5573-5

  66. Marr, L.C., Kirchstetter, T.W., Harley, R.A., Miguel, A.H., Hering, S.V., Hammond, S.K. (1999). Characterization of polycyclic aromatic hydrocarbons in motor vehicle fuels and exhaust emissions. Environ. Sci. Technol. 33, 3091–3099. https://doi.org/10.1021/es981227l

  67. Mehmood, T., Zhu, T., Ahmad, I., Li, X. (2020). Ambient PM2.5 and PM10 bound PAHs in Islamabad, Pakistan: Concentration, source and health risk assessment. Chemosphere 257, 127187. https://doi.org/10.1016/j.chemosphere.2020.127187

  68. Miguel, A.H., Kirchstetter, T.W., Harley, R.A., Hering, S.V. (1998). On-road emissions of particulate polycyclic aromatic hydrocarbons and black carbon from gasoline and diesel vehicles. Environ. Sci. Technol. 32, 450–455. https://doi.org/10.1021/es970566w

  69. Ministry of Environment (MOENV) (2020). Air Quality Standards.

  70. Ngo, T.H., Yang, H.Y., Pan, S.Y., Chang, M.B., Chi, K.H. (2022). Condensable and filterable particulate matter emission of coal fired boilers and characteristics of PM2.5-bound polycyclic aromatic hydrocarbons in the vicinity. Fuel 308, 121833. https://doi.org/10.1016/j.fuel.2021.121833

  71. Nisbet, I.C., Lagoy, P.K. (1992). Toxic equivalency factors (TEFs) for polycyclic aromatic hydrocarbons (PAHs). Regul. Toxicol. Pharmacol. 16, 290–300. https://doi.org/10.1016/0273-2300(92)90009-X

  72. Norris, G., Duvall, R., Brown, S., Bai, S. (2014). EPA positive matrix factorization (PMF) 5.0 fundamentals and user guide. U.S. Environmental Protection Agency EPA/600/R-14/108. 

  73. Ohura, T., Amagai, T., Sugiyama, T., Fusaya, M., Matsushita, H. (2004). Characteristics of particle matter and associated polycyclic aromatic hydrocarbons in indoor and outdoor air in two cities in Shizuoka, Japan. Atmos. Environ. 38, 2045–2054. https://doi.org/10.1016/j.atmosenv.2004.​01.038

  74. Park, R.J., Kim, M.J., Jeong, J.I., Youn, D., Kim, S. (2010). A contribution of brown carbon aerosol to the aerosol light absorption and its radiative forcing in East Asia. Atmos. Environ. 44, 1414–1421. https://doi.org/10.1016/j.atmosenv.2010.01.042

  75. Petit, J.E., Favez, O., Albinet, A., Canonaco, F. (2017). A user-friendly tool for comprehensive evaluation of the geographical origins of atmospheric pollution: Wind and trajectory analyses. Environ. Model. Softw. 88, 183–187. https://doi.org/10.1016/j.envsoft.2016.11.022

  76. Pham, C.T., Boongla, Y., Nghiem, T.D., Le, H.T., Tang, N., Toriba, A., Hayakawa, K. (2019). Emission characteristics of polycyclic aromatic hydrocarbons and nitro-polycyclic aromatic hydrocarbons from open burning of rice straw in the North of Vietnam. Int. J. Environ. Res. Public Health 16, 2343. https://doi.org/10.3390/ijerph16132343

  77. Polissar, A.V., Hopke, P.K., Poirot, R.L. (2001). Atmospheric aerosol over vermont:  chemical composition and sources. Environ. Sci. Technol. 35, 4604–4621. https://doi.org/10.1021/​es0105865

  78. Pongkiatkul, P., Kim Oanh, N.T. (2007). Assessment of potential long-range transport of particulate air pollution using trajectory modeling and monitoring data. Atmos. Res. 85, 3–17. https://doi.org/10.1016/j.atmosres.2006.10.003

  79. Pongpiachan, S., Tipmanee, D., Khumsup, C., Kittikoon, I., Hirunyatrakul, P. (2015). Assessing risks to adults and preschool children posed by PM2.5-bound polycyclic aromatic hydrocarbons (PAHs) during a biomass burning episode in Northern Thailand. Sci. Total Environ. 508, 435–444. https://doi.org/10.1016/j.scitotenv.2014.12.019

  80. Pope, C.A., Dockery, D.W. (2006). Health effects of fine particulate air pollution: lines that connect. J. Air Waste Manage. Assoc. 56, 709–742. https://doi.org/10.1080/10473289.2006.10464485

  81. Ravindra, K., Bencs, L., Wauters, E., de Hoog, J., Deutsch, F., Roekens, E., Bleux, N., Berghmans, P., Van Grieken, R. (2006). Seasonal and site-specific variation in vapour and aerosol phase PAHs over Flanders (Belgium) and their relation with anthropogenic activities. Atmos. Environ. 40, 771–785. https://doi.org/10.1016/j.atmosenv.2005.10.011

  82. Ravindra, K., Sokhi, R., Van Grieken, R. (2008). Atmospheric polycyclic aromatic hydrocarbons: Source attribution, emission factors and regulation. Atmos. Environ. 42, 2895–2921. https://doi.org/10.1016/j.atmosenv.2007.12.010

  83. Rohr, A.C., Wyzga, R.E. (2012). Attributing health effects to individual particulate matter constituents. Atmos. Environ. 62, 130–152. https://doi.org/10.1016/j.atmosenv.2012.07.036

  84. Room, S.A., Lin, C.E., Pan, S.Y., Hsiao, T.C., Chou, C.C.K., Chi, K.H. (2023). Incremental lifetime cancer risk of PAHs in PM2.5 via local emissions and long-range transport during winter. Aerosol Air Qual. Res. 23, 220319. https://doi.org/10.4209/aaqr.220319

  85. Schoeny, R., Poirier, K. (1993). Provisional guidance for quantitative risk assessment of polycyclic aromatic hydrocarbons. U.S. Environmental Protection Agency, Office of Research and Development, Office of Health and Environmental Assessment, Washington, DC, EPA/600/R-93/089 (NTIS PB94116571). 

  86. Shen, H., Huang, Y., Wang, R., Zhu, D., Li, W., Shen, G., Wang, B., Zhang, Y., Chen, Y., Lu, Y., Chen, H., Li, T., Sun, K., Li, B., Liu, W., Liu, J., Tao, S. (2013). Global atmospheric emissions of polycyclic aromatic hydrocarbons from 1960 to 2008 and future predictions. Environ. Sci. Technol. 47, 6415–6424. https://doi.org/10.1021/es400857z

  87. Sicre, M.A., Marty, J.C., Saliot, A., Aparicio, X., Grimalt, J., Albaiges, J. (1987). Aliphatic and aromatic hydrocarbons in different sized aerosols over the Mediterranean Sea: Occurrence and origin. Atmos. Environ. 21, 2247–2259. https://doi.org/10.1016/0004-6981(87)90356-8

  88. Soclo, H.H., Garrigues, P., Ewald, M. (2000). Origin of polycyclic aromatic hydrocarbons (PAHs) in coastal marine sediments: case studies in Cotonou (Benin) and Aquitaine (France) areas. Mar. Pollut. Bull. 40, 387–396. https://doi.org/10.1016/S0025-326X(99)00200-3

  89. Soleimani, M., Ebrahimi, Z., Mirghaffari, N., Moradi, H., Amini, N., Poulsen, K.G., Christensen, J.H. (2022). Seasonal trend and source identification of polycyclic aromatic hydrocarbons associated with fine particulate matters (PM2.5) in Isfahan City, Iran, using diagnostic ratio and PMF model. Environ. Sci. Pollut. Res. 29, 26449–26464. https://doi.org/10.1007/s11356-021-17635-8

  90. Song, N., Ma, J., Yu, Y., Yang, Z., Li, Y. (2015). New observations on PAH pollution in old heavy industry cities in northeastern China. Environ. Pollut. 205, 415–423. https://doi.org/10.1016/j.​envpol.2015.07.005

  91. Squizzato, S., Masiol, M., Agostini, C., Visin, F., Formenton, G., Harrison, R.M., Rampazzo, G. (2016). Factors, origin and sources affecting PM1 concentrations and composition at an urban background site. Atmos. Res. 180, 262–273. https://doi.org/10.1016/j.atmosres.2016.06.002

  92. Stein, A.F., Draxler, R.R., Rolph, G.D., Stunder, B.J.B., Cohen, M.D., Ngan, F. (2015). NOAA’s HYSPLIT atmospheric transport and dispersion modeling system. Bull. Am. Meteorol. Soc. 96, 2059–2077. https://doi.org/10.1175/BAMS-D-14-00110.1

  93. Strawa, A.W., Kirchstetter, T.W., Hallar, A.G., Ban-Weiss, G.A., McLaughlin, J.P., Harley, R.A., Lunden, M.M. (2010). Optical and physical properties of primary on-road vehicle particle emissions and their implications for climate change. J. Aerosol Sci. 41, 36–50. https://doi.org/​10.1016/j.jaerosci.2009.08.010

  94. Sugiyama, T., Shimada, K., Miura, K., Lin, N.H., Kim, Y. P., Chan, C.K., Takami, A., Hatakeyama, S. (2017). Measurement of ambient PAHs in Kumamoto: differentiating local and transboundary air pollution. Aerosol Air Qual. Res. 17, 3106–3118. https://doi.org/10.4209/aaqr.2016.12.0585

  95. Sun, J., Shen, Z., Zeng, Y., Niu, X., Wang, J., Cao, J., Gong, X., Xu, H., Wang, T., Liu, H., Yang, L. (2018). Characterization and cytotoxicity of PAHs in PM2.5 emitted from residential solid fuel burning in the Guanzhong Plain, China. Environ. Pollut. 241, 359–368. https://doi.org/10.1016/​j.envpol.2018.05.076

  96. Taghvaee, S., Sowlat, M.H., Hassanvand, M.S., Yunesian, M., Naddafi, K., Sioutas, C. (2018). Source-specific lung cancer risk assessment of ambient PM2.5-bound polycyclic aromatic hydrocarbons (PAHs) in central Tehran. Environ. Int. 120, 321–332. https://doi.org/10.1016/j.envint.2018.08.003

  97. Tai, H.H., Chang, Y.H. (2022). Reducing pollutant emissions from vessel maneuvering in port areas. Marit. Econ. Logist. 24, 651–671. https://doi.org/10.1057/s41278-022-00218-w

  98. Tan, J.H., Bi, X.H., Duan, J.C., Rahn, K.A., Sheng, G.Y., Fu, J.M. (2006). Seasonal variation of particulate polycyclic aromatic hydrocarbons associated with PM10 in Guangzhou, China. Atmos. Res. 80, 250–262. https://doi.org/10.1016/j.atmosres.2005.09.004

  99. Teixeira, E.C., Agudelo-Castañeda, D.M., Fachel, J.M.G., Leal, K.A., Garcia, K.D.O., Wiegand, F. (2012). Source identification and seasonal variation of polycyclic aromatic hydrocarbons associated with atmospheric fine and coarse particles in the Metropolitan Area of Porto Alegre, RS, Brazil. Atmos. Res. 118, 390–403. https://doi.org/10.1016/j.atmosres.2012.07.004

  100. Tomaz, S., Shahpoury, P., Jaffrezo, J.L., Lammel, G., Perraudin, E., Villenave, E., Albinet, A. (2016). One-year study of polycyclic aromatic compounds at an urban site in Grenoble (France): Seasonal variations, gas/particle partitioning and cancer risk estimation. Sci. Total Environ. 565, 1071–1083. https://doi.org/10.1016/j.scitotenv.2016.05.137

  101. U.S. Environmental Protection Agency (U.S. EPA) (2017). Toxicological Review of Benzo[a]pyrene (External Review Draft). U.S. Environmental Protection Agency, Washington, DC, EPA/635/R-14/312, 2014. 

  102. Van Drooge, B.L., Fernández, P., Grimalt, J.O., Stuchlík, E., Torres García, C.J., Cuevas, E. (2010). Atmospheric polycyclic aromatic hydrocarbons in remote European and Atlantic sites located above the boundary mixing layer. Environ. Sci. Pollut. Res. 17, 1207–1216. https://doi.org/​10.1007/s11356-010-0296-0

  103. Varea, M., Galindo, N., Gil-Moltó, J., Pastor, C., Crespo, J. (2011). Particle-bound polycyclic aromatic hydrocarbons in an urban, industrial and rural area in the western Mediterranean. J. Environ. Monit. 13, 2471. https://doi.org/10.1039/c1em10163c

  104. Vlachou, A., Tobler, A., Lamkaddam, H., Canonaco, F., Daellenbach, K.R., Jaffrezo, J.L., Minguillón, M.C., Maasikmets, M., Teinemaa, E., Baltensperger, U., El Haddad, I., Prévôt, A.S.H. (2019). Development of a versatile source apportionment analysis based on positive matrix factorization: a case study of the seasonal variation of organic aerosol sources in Estonia. Atmos. Chem. Phys. 19, 7279–7295. https://doi.org/10.5194/acp-19-7279-2019

  105. Wang, C.Y., Lim, B.S., Wang, Y.H., Huang, Y.C. (2021). Identification of high personal PM2.5 exposure during real time commuting in the Taipei metropolitan area. Atmosphere 12, 396. https://doi.org/10.3390/atmos12030396

  106. Wang, Q., Kobayashi, K., Lu, S., Nakajima, D., Wang, W., Zhang, W., Sekiguchi, K., Terasaki, M. (2016a). Studies on size distribution and health risk of 37 species of polycyclic aromatic hydrocarbons associated with fine particulate matter collected in the atmosphere of a suburban area of Shanghai city, China. Environ. Pollut. 214, 149–160. https://doi.org/10.1016/j.envpol.2016.04.002

  107. Wang, Q., Liu, M., Yu, Y., Li, Y. (2016b). Characterization and source apportionment of PM2.5-bound polycyclic aromatic hydrocarbons from Shanghai city, China. Environ. Pollut. 218, 118–128. https://doi.org/10.1016/j.envpol.2016.08.037

  108. Wang, S.H., Hung, W.T., Chang, S.C., Yen, M.C. (2016c). Transport characteristics of Chinese haze over Northern Taiwan in winter, 2005–2014. Atmos. Environ. 126, 76–86. https://doi.org/​10.1016/j.atmosenv.2015.11.043

  109. Wang, X.T., Miao, Y., Zhang, Y., Li, Y.C., Wu, M.H., Yu, G. (2013). Polycyclic aromatic hydrocarbons (PAHs) in urban soils of the megacity Shanghai: Occurrence, source apportionment and potential human health risk. Sci. Total Environ. 447, 80-89. https://doi.org/10.1016/j.scitotenv.​2012.12.086

  110. Watson, J.G. (2002). Visibility: science and regulation. J. Air Waste Manage. Assoc. 52, 628–713. https://doi.org/10.1080/10473289.2002.10470813

  111. Wei, C., Han, Y., Bandowe, B. A. M., Cao, J., Huang, R.J., Ni, H., Tian, J., Wilcke, W. (2015). Occurrence, gas/particle partitioning and carcinogenic risk of polycyclic aromatic hydrocarbons and their oxygen and nitrogen containing derivatives in Xi'an, central China. Sci. Total Environ. 505, 814–822. https://doi.org/10.1016/j.scitotenv.2014.10.054

  112. World Health Organization (WHO) (2000). Air Quality Guidelines for Europe. In: World Health Organization Regional Office for Europe Copenhagen, Denmark.

  113. World Health Organization (WHO) (2022). Ambient (outdoor) air pollution. (accessed 5 February 2023).

  114. Wu, Y., Yang, L., Zheng, X., Zhang, S., Song, S., Li, J., Hao, J. (2014). Characterization and source apportionment of particulate PAHs in the roadside environment in Beijing. Sci. Total Environ. 470–471, 76–83. https://doi.org/10.1016/j.scitotenv.2013.09.066

  115. Yang, L., Wang, W.C., Lung, S.C. C., Sun, Z., Chen, C., Chen, J.K., Zou, Q., Lin, Y.H., Lin, C.H. (2017). Polycyclic aromatic hydrocarbons are associated with increased risk of chronic obstructive pulmonary disease during haze events in China. Sci. Total Environ. 574, 1649–1658. https://doi.org/10.1016/j.scitotenv.2016.08.211

  116. Yang, L., Zhang, X., Xing, W., Zhou, Q., Zhang, L., Wu, Q., Zhou, Z., Chen, R., Toriba, A., Hayakawa, K., Tang, N. (2021). Yearly variation in characteristics and health risk of polycyclic aromatic hydrocarbons and nitro-PAHs in urban shanghai from 2010–2018. J. Environ. Sci. 99, 72–79. https://doi.org/10.1016/j.jes.2020.06.017

  117. Yu, H., Guo, T., Wu, Z., Lin, T., Hu, L., Guo, Z. (2021). Distribution and gas-particle partitioning of polycyclic aromatic hydrocarbons over the East China Sea and Yellow Sea in spring: Role of atmospheric transport transition. Sci. Total Environ. 762, 143071. https://doi.org/10.1016/j.​scitotenv.2020.143071

  118. Yu, K.P., Yang, K.R., Chen, Y.C., Gong, J.Y., Chen, Y.P., Shih, H.C., Lung, S.C.C. (2015). Indoor air pollution from gas cooking in five Taiwanese families. Build Environ. 93, 258–266. https://doi.org/10.1016/j.buildenv.2015.06.024

  119. Yu, Q., Yang, W., Zhu, M., Gao, B., Li, S., Li, G., Fang, H., Zhou, H., Zhang, H., Wu, Z., Song, W., Tan, J., Zhang, Y., Bi, X., Chen, L., Wang, X. (2018). Ambient PM2.5-bound polycyclic aromatic hydrocarbons (PAHs) in rural Beijing: Unabated with enhanced temporary emission control during the 2014 APEC summit and largely aggravated after the start of wintertime heating. Environ. Pollut. 238, 532–542. https://doi.org/10.1016/j.envpol.2018.03.079

  120. Yunker, M.B., Macdonald, R.W., Vingarzan, R., Mitchell, R.H., Goyette, D., Sylvestre, S. (2002). PAHs in the Fraser River basin: a critical appraisal of PAH ratios as indicators of PAH source and composition. Org. Geochem. 33, 489–515. https://doi.org/10.1016/S0146-6380(02)00002-5

  121. Zhang, Y., Tao, S., Cao, J., Coveney, R.M. (2007). Emission of polycyclic aromatic hydrocarbons in China by county. Environ. Sci. Technol. 41, 683–687. https://doi.org/10.1021/es061545h

  122. Zhang, Y., Chen, J., Yang, H., Li, R., Yu, Q. (2017). Seasonal variation and potential source regions of PM2.5-bound PAHs in the megacity Beijing, China: Impact of regional transport. Environ. Pollut. 231, 329–338. https://doi.org/10.1016/j.envpol.2017.08.025

  123. Zhang, Y., Zheng, H., Zhang, L., Zhang, Z., Xing, X., Qi, S. (2019). Fine particle-bound polycyclic aromatic hydrocarbons (PAHs) at an urban site of Wuhan, central China: Characteristics, potential sources and cancer risks apportionment. Environ. Pollut. 246, 319–327. https://doi.org/10.1016/​j.envpol.2018.11.111

  124. Zhao, P., Yu, K.P., Lin, C.C. (2011). Risk assessment of inhalation exposure to polycyclic aromatic hydrocarbons in Taiwanese workers at night markets. Int. Arch. Occup. Environ. Health 84, 231–237. https://doi.org/10.1007/s00420-010-0551-1

  125. Zhou, H., Wu, C., Onwudili, J.A., Meng, A., Zhang, Y., Williams, P.T. (2014). Polycyclic aromatic hydrocarbon formation from the pyrolysis/gasification of lignin at different reaction conditions. Energy Fuels 28, 6371–6379. https://doi.org/10.1021/ef5013769

  126. Zhou, K., Yang, S. (2016). Emission reduction of China׳s steel industry: Progress and challenges. Renewable Sustainable Energy Rev. 61, 319–327. https://doi.org/10.1016/j.rser.2016.04.009 

Share this article with your colleagues 


Subscribe to our Newsletter 

Aerosol and Air Quality Research has published over 2,000 peer-reviewed articles. Enter your email address to receive latest updates and research articles to your inbox every second week.

77st percentile
Powered by
   SCImago Journal & Country Rank

2022 Impact Factor: 4.0
5-Year Impact Factor: 3.4

Call for Papers for the special issue on: "Carbonaceous Aerosols in the Atmosphere"

Aerosol and Air Quality Research partners with Publons

CLOCKSS system has permission to ingest, preserve, and serve this Archival Unit
CLOCKSS system has permission to ingest, preserve, and serve this Archival Unit

Aerosol and Air Quality Research (AAQR) is an independently-run non-profit journal that promotes submissions of high-quality research and strives to be one of the leading aerosol and air quality open-access journals in the world. We use cookies on this website to personalize content to improve your user experience and analyze our traffic. By using this site you agree to its use of cookies.