Particle Associated Polycyclic Aromatic Hydrocarbons (PAHS) in Urban Air of Agra

Total Suspended Particulate Matter (TSPM) samples were collected at Nunhai Agra from April to September 2006. The concentrations of 16 PAHs in aerosols were quantified. The dominated predominant PAHs in TSPM include high molecular weight (HMW) congeners BghiP, DbA, IP and BaP. Nap and Acy were not detected in any of the samples. The sum of 14 priority PAHs ranged from 150 to 480 ng m^?3 with a mean value of 269 ± 121 ng m^?3. The Results indicated that PAH concentrations at Nunhai were higher than in other industrial sites, but are comparable to those measured in several urban Chinese cities, however, and less than the industrial locations of China. Higher HMW PAH concentration were attributable to higher rates of emissions as well as or greater scavenging and adsorption of vapor phase PAH on available TSPM. Potential sources of PAHs in aerosols were identified using the diagnostic ratios between PAHs. Vehicular emissions were the main contributors of particulate-associated PAHs, with minor contribution from stationary combustion sources may also contribute to the particulate PAHs. PAHs in aerosols were predominantly from gasoline and diesel engines.     

Monitoring and Assessment of Polycyclic Aromatic Hydrocarbons (PAHs) in the Atmosphere of Alexandria City,Egypt

The concentrations of 16 polycyclic aromatic hydrocarbons (PAHs) in the total suspended particulate (TSP) were measured simultaneously between January 30, 2015 and February 11, 2016 at urban, suburb, and rural sites at Alexandria City, Egypt, using pesticide samplers. Samples were extracted and analyzed using chromatography–mass spectrometric (GC–MS). There was a significant difference in concentrations between the three sites, and between particle- and vapor-phases. Mean total PAH concentrations were 502.48, 322.57, and 417.23 ng m^?3 for the urban, the rural, and the suburban sites in particulate-phase and were 723.49, 402.26, and 543.15 for the same sites in vapor-phase, respectively. At the three sites, the most abundant compounds determined were Benzo[k]fluoranthene (BkF), followed by Benzo[a]pyrene (BaP) and Indeno [1,2,3-cd] pyrene (IcdP). These high molecular weight compounds are carcinogenic and known to originate mainly from vehicular emissions. The diagnostic ratios indicated PAHs in urban and suburban sites were predominantly from gasoline and diesel engines, while that in rural site was from biomass burning. Characterization of the emission sources was further substantiated by significant correlation between individual PAH species.     

Distribution and Sources of Polycyclic Aromatic Hydrocarbons (PAHs) in Surface Sediments from the Northern Part of the Persian Gulf (Hormuzgan Province)

Sediments from the intertidal areas of Hormuzgan province in northern part of Persian Gulf (Iran) were investigated for the levels and possible sources of 15 polycyclic aromatic hydrocarbons (PAHs). Samples of sediments were collected from twelve sampling sites and analyzed for PAHs by gas chromatography–mass spectrometry (GC-MS). The results showed that the total concentrations of PAHs ranged from 765 to 1898 ng/g dry weight. Composition pattern in the sediment samples from 12 sampling sites was dominated by 4-ring PAH compounds. Molecular indices based on ratios of PAH concentrations were used to differentiate PAHs from pyrolitic, petrogenic and mixed origins. The results of study suggested that the main sources of PAHs in the sediment were mixed with pyrolitic and petrogenic inputs. According to the US sediments quality guidelines (SQGs) (ERL/ERM) sediments of the mentioned region did not show any ecotoxicological risk for benthic organisms.     

Sources and Health Risk of Organic Compounds in Respirable Particles in Tehran,Iran

Forty-one respirable particle (PM₄) samples were collected from October 2011 through March 2012. This timespan covered the fall and winter seasons in Tehran, Iran. The associated polycyclic aromatic hydrocarbon (PAH) and n-alkane concentrations were analyzed to investigate the sources of these compounds and health risks of the former. The average total PAH and n-alkane concentrations were 16.2 ng/m³ and 758 ng/m³, respectively. The most abundant PAHs were 2- and 3-ring compounds, while the most abundant n-alkanes were nC₁₆ and nC₁₈. The results of source identification by factor analysis (FA) are consistent with and complementary to those from diagnostic ratios (DRs). The PAH DRs indicate a dominant contribution from pyrogenic sources, in particular diesel engines from local traffic sources, while FA reveals a diesel-fuelled vehicle emission related factor, a gasoline engine emission-related factor, an industrial source factor and a wood combustion, incineration and tire tread source factor. The n-alkane DRs indicate dominant contributions from anthropogenic sources or vehicular emissions, while FA reveals a fossil fuel combustion factor and a biogenic source factor. Although the average BaP concentration was below the Iran Department of Environment's annual average standard of 1 ng/m³, the BaP-equivalent concentration of the PAHs (BaP_PEQ) indicates harmful effects cannot be ruled out. The ICR_L and ICR_U data suggests a potential cancer risk incidence of about 1–54 individuals per million in the population from a lifetime of 70 years inhalation of particle associated PAHs in Tehran. These findings highlight the importance of reducing emissions from traffic, in particular emissions from diesel-fuelled vehicles, in Tehran.     

Characteristics of Polynuclear Aromatic Hydrocarbons in Ambient Air through a Long-Term Sampling Program at a Metropolitan City in Taiwan

Polynuclear aromatic hydrocarbon (PAH) concentrations in total suspended particulate (TSP) matter as well as gaseous PAH contents are measured at an urban site adjacent to the capital of Taiwan. Several factors, such as seasonal variation, ring number, G/P (gas/particulate) ratio, and C-atom number, are utilized to characterize the pollution features of 14 PAHs. The results show that the total PAH content in TSP has been reduced gradually. The probable carcinogenic PAH compounds exist primarily in the particulate phase. The concentration distributions of each PAH compound are different, and the quantities and ring distributions of PAHs are significantly affected by seasonal fluctuation. The G/P ratio is highly associated with the C-atom number of PAHs. Factor analysis, along with the characteristic ratios of PAHs, is used to qualitatively identify the probable contributors. The results suggest that traffic exhaust and industrial origins are the predominant contributors.     

Levels of Polycyclic Aromatic Hydrocarbons (PAHs) in Atmospheric Environment of Urban Areas in Latin America

Polycyclic aromatic hydrocarbons (PAHs) are chemical compounds considered as pollutants of high priority due to their carcinogenic potential. PAH can appear in water, soil or in the atmosphere as adsorbed on particulate material or in gas phase. An increased number of studies on atmospheric PAH in urban areas have been published in the last decade, especially in the last years. Anthropogenic sources are frequently mentioned to be responsible for the increased concentration of PAHs in the atmosphere of urban areas, which at the same time seems to depend on meteorological parameters. This research is focused on compiling information on PAH levels in Latin America and their relationship with typical meteorological variables from seasonal and tropical countries. Brazil is the country with the most number of bibliographies about this topic, followed by Argentina, Chile and Mexico. Scarce information was found for Colombia and Venezuela and none for the rest of Latin American countries. The majority of studies checked have evaluated the climatological parameters in relationship with the PAH concentration and their distribution, finding that it affects meaningfully their levels. The monitor campaigns in Brazil have been developed mainly in the southern cities, where PAHs are strongly influenced by the seasons and their proximity to the South Pole. Tropical countries such as Venezuela and Colombia showed moderate variation of PAH concentration through months. The main influential parameters are precipitation and direction/speed winds.     

Beyond 16 Priority Pollutant PAHs: A Review of PACs used in Environmental Forensic Chemistry

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous in soils and sediments, particularly in urbanized environments in which the concentrations of 16 (or so) PAHs are regulated. Distinguishing among the numerous PAH sources is of practical and legal concern and thereby is often an objective of environmental forensic chemistry studies. Studies of prospective sources and impacted soils and sediments that rely upon the 16 U.S. EPA Priority Pollutant PAHs are disadvantaged, as these few compounds generally lack the specificity to distinguish among different PAH sources in the environment. Advances in analytical and interpretive methods over several decades have shown that different PAH sources can be more defensibly distinguished using modified EPA Method 8270 that, among other improvements, measure many other polycyclic aromatic compounds (PACs) that co-occur with the Priority Pollutant PAHs in different sources and in the environment. The PACs include variously-alkylated PAHs and polycyclic aromatic sulfur heterocyclics (PASHs) homologs and individual isomers, which are herein reviewed. Collectively, these PACs provide a higher degree of specificity among PAC sources and can be used to understand the effects of weathering on PAH assemblages. Despite their diagnostic capacity, PACs should not be relied upon at the exclusion of other compound groups (e.g., petroleum biomarkers) in most environmental forensic chemistry studies. In light of these advances, source characterization studies that rely only upon the 16 (or so) Priority Pollutant PAHs warrant considerable caution.     

Gas-Particle Partitioning of PAHs In The Urban Air of Dalian,China: Measurements and Assessments

To evaluate the gas-particle partitioning behavior of polycyclic aromatic hydrocarbons (PAHs) in the urban air of Dalian, China, both gas phase and particle phase ambient air were monitored with active high-volume sampler from November 2009 to October 2010. The average total concentration of 16 US EPA priority monitoring PAHs (particle + gas) (∑PAHs) was 112 ng m^?3 and the most abundant PAH was Phenanthrene. ∑PAHs and the gas-particle partitioning coefficients (K _p) of PAHs displayed seasonal variation in the order of winter > autumn > spring > summer. ∑PAHs was much higher during the heating period than non heating period. ∑PAHs in gas phase were all higher than those in particle phase in the four seasons. The PAHs sources identification was attempted using diagnostic ratios. The relationship between the concentration of PAHs in the air and meteorology parameters were analyzed using SPSS packages. The concentrations of PAHs in the air decreased with the increase of ambient temperature, and increased with the increase of atmospheric pressure. The gas-particle distribution was examined through several different approaches such as the relationship of logK _p with the ambient temperature, with the logarithm of the sub-cooled vapor pressure (logP _L ⁰), and the octanol-air partitioning coefficient (logK _oa) of PAHs. The slopes obtained from regressing logK _p vs. logP _L ⁰ was ?0.687～?0.821 in heating periods, which was in the range between ?0.6 and ?1, indicating the partitioning of PAHs to particle phase in the urban air of Dalian was absorption as well as for adsorption mechanism. However, the average slope value was ?0.502 in the non heating periods, which was shallower than -0.60, indicating that the absorption mechanisms contributed more to the partitioning process. The exposure risk of PAHs was evaluated with four methods, the results of which indicated that the quality of the urban air of Dalian was better.     

Levels and Origin of PAHs in Some Big Lakes

This study was designed to assess the contamination of a very special lake, Lake Baikal in Siberia, and two big lakes, Ladoga and Onega in the European part of Russia, by polycyclic aromatic hydrocarbons (PAHs). PAH compounds were analyzed by HPLC and the target PAH, benzo[ a ]pyrene (B a P), by using the spectral-luminescence (Shpol'skii) method. Elevated levels (to 96 w g kg m 1 ) of B a P in sediments of Lake Baikal reflected proximity to potential sources of emission, situated either on shore (a paper and pulp mill in Baikalsk) or upstream river systems. The concentration of B a P in sediments decreased with the distance from outlet and the depth. The sediment samples contained several representatives of PAHs. The total content of identified compounds reached 873 w g kg m 1 (less than four nuclear representatives not included). Dominating heavy PAHs were dibenz[ a,j ]anthracene, dibenz[ a,h ]anthracene, dibenzo[ a,e ]pyrene, and dibenzo[ a,l ]pyrene. The concentration of B a P in sediments of northeastern Baikal was more than two times less than that for the southern part of the lake and corresponds to the background level. The B a P levels estimated for sediments close to paper and pulp mills of the Lake Ladoga exceeded 160 w g kg m 1 , being two orders of magnitude higher than that for other areas of these lakes. The contamination of sediments of Lake Onega by PAHs is affected by pulp and paper mills as well as other sources. Our results clearly demonstrate the contribution of specific industrial sources like paper and pulp mills to the content of PAHs in the Baikal, Ladoga, and Onega water ecosystem.     

Polycyclic aromatic hydrocarbon emissions of non-road diesel engine treated with non-thermal plasma technology

Non-road diesel engines are important polycyclic aromatic hydrocarbon (PAH) sources in the environment due to their high emission concentration compared to on-road diesel engines. Particle- and gas-phase PAH concentrations of a non-road diesel engine were investigated. Non-thermal plasma (NTP) as an effective after-treatment technology was used to reduce PAH emissions. The results showed that particle-phase PAH concentrations were 329.7 µg/m³, 3,206.7 µg/m³, and 1,185.7 µg/m³ without the action of NTP at three different engine loads respectively. Relatively low concentrations were measured for gas-phase PAHs. Excellent linearity was shown for particle-phase with total PAH concentrations both with, and without, NTP. The gas-phase PAH concentrations linearly increased with engine load without NTP. The five most abundant compounds of PAHs were among low molecular weight (LMW) and medium molecular weight (MMW) compounds. Total PAH cleaning efficiency was beyond 50% when treated with NTP at the three different engine loads. We hypothesized that naphthalene (Nap) concentrations increased greatly at 60% and 80% engine loads because it was produced within the plasma zone by decomposition of high molecular weight (HMW) PAHs. The PAHs content of particulate matter (PM) aggregation at 60% load was approximately three times higher than at 40% and 80% loads. High correlation values were observed for MMW PAHs with total PAH concentrations. Correlations of PAH concentration reduction could be important to clarify the PAH reduction mechanism with NTP technology.     

Priority Polycyclic Aromatic Hydrocarbons (PAHs): Distribution,Possible Sources and Toxicity Equivalency in Urban Drains

Wastewater from urban areas constitutes one of the major sources of pollutants contributed to aquatic ecosystem. This study was carried out to elucidate the occurrence and possible source of US Environmental Protection Agency identified 16 priority polycyclic aromatic hydrocarbons (PAHs) in water and sediments from the urban wastewater drains in Delhi, India. A total 60 samples (water and sediment) collected during year 2011–2012, and analyzed the following USEPA methods. Water and sediment samples were extracted using liquid-liquid and ultrasonication techniques, respectively. Glass column chromatography with activated silica was used for sample extracts clean-up, followed by quantification on HPLC equipped with diode array detector at 254 nm wavelength using mixture of acetonitrule and water as mobile phase. Concentrations of total 16 PAHs (∑16PAHs) in all drain water samples ranged from 0.29–35.22 μg/L (mean ± SD, 10.83 ± 10.66 μg/L), predominated by two- and three -ring PAHs. The ∑16PAHs concentrations in all collected sediments ranged between 220–19321 μg/kg (mean±SD, 5574 ± 6820 μg/kg) dry weights. High molecular weight PAHs (≥4-ring PAHs) were dominant in sediment samples. Benzo(a)pyrene equivalent (BaPeq), a relative carcinogenic potential to the corresponding PAHs to BaP was estimated and presented. A selected number of concentration ratios of specific PAHs compounds were calculated and used to diagnose the possible sources of PAHs contamination. The diagnostic ratios reflected pyrogenic input from gasoline or diesel powered vehicular emissions as the major source of PAHs. The levels of PAHs observed in water and sediments were compared with similar studies undertaken in other regions of the world.     

Source characterization and the environmental impact of urban street dusts from Egypt based on hydrocarbon distributions

The aliphatic and aromatic fractions of the extracts of ten street dust (SD) samples collected from eight cities covering a wide geographic area of Egypt were analyzed using gas chromatography with flame ionization detector (GC-FID) and GC-MS to compare their hydrocarbon distributions. To identify their sources, the extracts of the possible source materials were also analyzed. The impact of SDs on the marine environment was investigated in a marine sediment collected from the Western Harbor of Alexandria. The GC-FID profiles of the aliphatic fractions showed considerable differences in the n-alkane distribution that permits the classification of the SDs into five groups. This grouping reflects the environments of the cities in which they are collected. The carbon preference index and the unresolved complex mixture relative to the total resolved peaks values revealed that automobile exhaust is the main source of the hydrocarbons in these SDs with a significant contribution from terrestrial higher plant waxes to group 1 (Nile Delta cities). The sterane and hopane profiles supported this conclusion. The total polycyclic aromatic hydrocarbon (PAH) concentrations ranged from 27 to 379 ng/g (dry wt.) and showed clear differences between the SDs. The lowest and highest concentrations were found in samples from Shebeen and Port Said, respectively. The PAH distribution patterns and the ratio of the sum of combustion specific PAHs to total PAHs in samples from Alexandria, Port Said and Cairo were similar, implying similar sources. PAH ratios indicated a mixture of pyrogenic and petrogenic sources of PAHs in all samples where asphalt and automobile fuel exhaust were the major contributors of PAHs in Alexandria, Port Said, Cairo and Sharm El Sheikh cities. These ratios also indicated the predominance of diesel-operated vehicles to the PAHs signatures of Alexandria, Port Said and Cairo while gasoline emissions influence more strongly the PAH distributions in the SDs from Shebeen, Kafr El Sheikh and Sharkea. The PAH fingerprints excluded fresh oil and tire particles as major contributors. Both SDs and petrogenic sources significantly contributed to the hydrocarbon signature of the marine sediment from the Western Harbor of Alexandria.     

The Spatial and Temporal Variations of Polycyclic Aromatic Hydrocarbons (PAHs) in Environmental Matrices in the Czech Republic

The paper is a review of the PAH emission inventories and the results of ambient air measurements of PAHs on regional a local level and determination of PAHs in other abiotic and biotic samples in the Czech Republic (CR). The main sources of polycyclic aromatic hydrocarbons (PAHs) in the country are associated with electric and thermal energy production, waste incineration, road traffic and some industrial processes (e. g. high-temperature coal carbonation, catalytic cracking of crude oil and aluminium production).     

Characterization of Gaseous and Particulate Polycyclic Aromatic Hydrocarbons in Ambient Air of Delhi,India

Three seasonal sampling campaigns were undertaken at an urban site of Delhi for collection of PAHs in particulate and gas phase. Sampling was done by using modified Respirable Dust (PM ≤10μm) sampler attached with polyurethane foam (PUF) plugs and compared with conventional Respirable Dust (PM ≤10 μm) sampler. Total 16 EPA PAH (gaseous + particulate) were determined by Gas Chromatograph-Mass Spectrophotometer (GC-MS). The 3-ring PAH constitutes approximately 90% of the gaseous PAHs with phenanthrene, fluoranthene, acenapthylene, and acenaphthene being the most abundant gaseous PAHs. PAHs with 4- to 6- rings accounted for 92%, 87% and 78% in samples collected during winter, summer and monsoon season respectively. Gaseous PAHs, particulate PAHs and total PAHs were higher during winter as compared to summer and monsoon seasons. The contribution of particulate PAHs were 1.4, 2.1, and 2.5 times higher in winter, summer and monsoon, respectively than of gaseous PAHs. Indeno[123-cd]pyrene, benzo[ghi]perylene, dibenzo[ah]anthracene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene and chrysene were found to be the most abundant PAH compounds in the particulate PAHs during all the seasons. The result from application of diagnostic ratio suggests that the higher particulate PAHs emissions were predominantly associated with vehicular emissions along with emissions from biomass burning during winter season.     

Status of PAHs in Environmental Compartments of South Africa: A Country Report

This article covers the status of PAH concentrations and composition patterns in surface water, air, sediment, and soil samples from South Africa. Despite South Africa being one of the largest economies in Africa, it is only recently that researchers have reported the presence and possible sources of these compounds in various environmental compartments. This article discusses the potential hotspots and possible sources of these compounds. It also compares the total PAH concentrations and percentage composition patterns of the individual PAHs. So far, total concentrations of five PAHs determined in sediment samples from the Johannesburg area, Gauteng Province, gave the highest concentrations ranging from 1233–136,276 μg kg^?1. The total concentration of six PAHs found in runoff water from the Venda region of the Limpopo Province, gave the highest concentration with a range of 28.7–3192.6 μg L^?1. The decreasing order of percentage composition of PAHs in water samples tended to follow 3-ring > 4-ring > 2-ring PAHs. In soil samples the decreasing order of percentage composition followed 4-ring > 3-ring > 5-ring > 2-ring > 6-ring PAHs. The total freely dissolved PAHs followed solubility of the compounds with 2-ring > 3-ring > 4-ring > 5-ring > 6-ring PAHs. Some of the identified sources of PAHs using molecular ratios include petrogenic emissions such as from petroleum combustion from vehicles and pyrolytic sources such as coal combustion by coal powered power stations, as well as iron and steel production industries. Oil spills were also identified as major PAH contributor in runoff water from the Venda region of the Limpopo Province.     

Indices of PAH Origin—A Case Study of the Gulf of Gdańsk (SE Baltic) Sediments

The aim of this work is to present a way of developing indices for assessing the dominant origin of polycyclic aromatic hydrocarbons (PAHs) on the basis of a case study in the Gulf of Gdańsk (SE Baltic). The indices were based on selected concentration ratios of both parent and alkylated PAHs found in reference matrices that are potential anthropogenic sources of PAH pollution for this area, i.e., airborne particulate matter (PM10) from the Gdańsk conurbation, soot derived from wood and diesel oil combustion, and a variety of petrogenic products. Verification of the suitability of the PAH ratios for source apportionment showed that the following indices are potentially the most useful for distinguishing PAHs of pyrogenic and petrogenic origin: [Σ3-+Σ4-ring-PAHs]/[Σ5-+Σ6-ring-PAHs], ΣmMP/Phen, 4,5-MP/ΣmMP, 1,7-dMP/[1,7-+2,6-dMP]. It was found that PAHs deposited in recent sediments in the Gulf of Gdańsk originate mainly from pyrogenic sources, while perylene is also derived from diagenetic processes.     

Characterization of PM2.5-Bound Polycyclic Aromatic Hydrocarbons in the Ambient Air of Győr,Hungary

ABSTRACT

In Hungary, the nationwide monitoring of PM10-bound polycyclic aromatic hydrocarbons (PAHs) in ambient air is great importance for a number of reasons related to human health, the environment and compliance with European Union legislation. However, the measurement of PAH concentrations in PM2.5 aerosol fraction has not been carried out. Therefore, the concentration, distribution and sources of PM2.5-bound PAHs at different urban sites of Gy?r were investigated in a heating season. The total PAH concentrations (sum of 19 individual PAH compounds) ranged from 1.32 to 37.27 ng/m³ with the mean value of 10.54 ng/m³. The high molecular weight PAHs with 5 and 6 aromatic rings were the most abundant PAHs in PM2.5 aerosol samples, which averaged 82% of total PAHs. Using benzo(a)pyrene (BaP) equivalent approach on the concentration data of carcinogenic PAH species, BaP and indeno(1,2,3-cd)pyrene contributed the highest carcinogenic exposure equivalent (1.25 and 0.19 ng/m³ on average). However, the incremental lifetime cancer risk (ILCR) values for resident children and adults indicated low-potential cancer risk (ILCR < 10^?6). The source apportionment results reflected that the major sources of PAH compounds in the Gy?r atmosphere were fossil fuel combustion and vehicle emissions.     

Evaluation of Polycyclic Aromatic Hydrocarbons Contamination in the Sediments of the Johor Strait,Peninsular Malaysia

In May 2013, sediment samples were collected from five stations in the Straits of Johor, near the southern tip of Peninsular Malaysia, in order to evaluate the distribution and sources of polycyclic aromatic hydrocarbons (PAHs). The concentrations of 16 United States Environmental Protection Agency PAHs varied from 650.5 to 1441.2 ng g ^?1 dry weight (dw) with a mean value of 985.5 ng g ^?1 dw. PAHs can be classified as moderate level pollution in the collected samples. When comparing PAHs in this study with that of the sediment quality guidelines (SQGs), it was found that the total PAHs, low molecular weight (LMW), and high molecular weight (HMW) PAHs might incur minimal adverse biological effects. The diagnostic ratios of individual PAHs indicated both petrogenic and pyrogenic origins with predominantly pyrogenic sources, the findings of which are further supported by the results from principal component analysis (PCA). The PCA results reveal contributions of 44.44%, 32.3%, and 18.96% for traffic-related, coal combustion, and petroleum-related products, respectively. These findings indicate that the effective monitoring and significant improvement resulting from the implementation of environmental regulations in Malaysia might have caused a shift in the source of petroleum hydrocarbons in the Straits of Johor's aquatic ecosystems from petrogenic to pyrogenic origins.     

COMPARISON OF PAHS,NITRO-PAHS AND OXY-PAHS ASSOCIATED WITH AIRBORNE PARTICULATE MATTER AT ROADSIDE AND URBAN BACKGROUND SITES IN DOWNTOWN TOKYO,JAPAN

Atmospheric polycyclic aromatic hydrocarbons (PAHs), nitro-PAHs and oxy-PAHs are emitted from primary sources. Some nitro-PAHs and oxy-PAHs can also arise from secondary formation in the atmosphere. To assess the relative importance of these sources, the polycyclic aromatic compound (PAC) concentrations were determined at a roadside (Roadside site) and on a rooftop (Urban Background site) in downtown Tokyo Japan. The concentrations of PAHs, 1-nitropyrene and oxy-PAHs at the Roadside site were higher than those at the Urban Background site, while 2-nitrofluoranthene levels were the same at both sites. However, the mean ratios of concentrations at the Urban Background site to the Roadside site were in the order 1,8-naphthalic anhydride>9,10-anthraquinone>PAHs or 1-nitropyrene or acenaphthenequinone or benzanthrone. This suggests that in addition to vehicle emissions, a considerable fraction of some of the oxy-PAHs studied originates from another source, which might be secondary formation by atmospheric PAH degradation, and this contribution varied among the oxy-PAHs.     

POLYCYCLIC AROMATIC HYDROCARBONS OF DIESEL AND GASOLINE EXHAUST AND DNA ADDUCT DETECTION IN CALF THYMUS DNA AND LYMPHOCYTE DNA OF WORKERS EXPOSED TO DIESEL EXHAUST

Particles present in urban air pollution are mainly derived from diesel- and gasoline-fueled vehicles. Exhaust emission is able to cause several health effects in humans including mutagenicity and carcinogenicity. Polycyclic aromatic hydrocarbons (PAHs) were measured in diesel and gasoline particulate extracts and DNA binding to CT DNA (±S9 and ±XO) was investigated. A large difference in content of 14 PAHs in diesel and gasoline extracts was observed, showing higher concentration of 14 PAHs, 6 carcinogenic PAHs, benzo[a]pyrene (B[a]P) in diesel than in gasoline extracts. Selected PAH standards of B[a]P, benzo[c]fluoranthene (B[c]F), and 3-nitrobenzanthrone (NBA) were used in ³²P-postlabeling/polyacrylamide gel electrophoresis (PAGE) technique to identify CT DNA adducts formed by diesel particulate extracts. CT DNA adduct formation was higher for diesel extracts in comparison with gasoline extracts; however, no clear origin of DNA adducts derived from B[c]F-, 3-NBA-, B[a]P was detected. ³²P-postlabeling/PAGE was a useful assay for analyzing and identifying PAH-DNA adducts. Occupational exposure to particulate and volatile PAH concentrations were evaluated using personal air samples and lymphocyte DNA adducts as markers of exposure. Overall air PAH concentrations were low in all eight workplaces, consisting of 97% of vapor phase compounds. DNA adducts analyzed by ³²P-postlabeling assay were compared between the butanol and nuclease P1 enrichment procedures. Only in winter samples of exposed workers, butanol extraction revealed significantly higher adduct levels in comparison with those of control persons. No differences in adduct levels between exposed and control persons in summer were detected by using either butanol extraction or nuclease P1 treatment. Total concentrations of particulate and volatile PAHs measured in eight workplaces in winter showed a significant correlation with total DNA adducts analyzed in workers' lymphocytes (r = 0.852N = 8, p = .007).