MEASUREMENT OF CONCENTRATIONS OF POLYCYCLIC AROMATIC HYDROCARBONS AND DIOXIN COMPOUNDS IN CANINE LUNGS

Polycyclic aromatic hydrocarbons (PAHs) and dioxin compounds remaining in canine lungs were measured with an alkaline decomposition method employing KOH/ethanol. PAHs extracted from the lungs of 31 dogs were between 0.07 and 0.47 ng/wet-g (mean: 0.19 ng/wet-g) for BaA; 0.03 and 0.16 ng/wet-g (mean: 0.08 ng/wet-g) for BkF; 0.05 and 0.29 ng/wet-g (mean: 0.13 ng/wet-g) for BaP; and 0.05 and 0.35 ng/wet-g (mean: 0.17 ng/wet-g) for BghiP. Dioxin concentrations were between 0.047 and 0.870 pg-TEQ/wet-g (mean: 0.179 pg-TEQ/wet-g). There were big differences between the PAH concentrations and dioxin concentrations in the canine lungs. Strong relationships were observed between individual PAHs (r = 0.73–0.95). In this study, we detected PAHs and dioxins in all samples, confirming that canine lungs were contaminated by those pollutants.     

POLYCYCLIC AROMATIC HYDROCARBONS IN THREE VARIETIES OF FISH FROM KUWAIT BAY

The study reports levels of parent polycyclic aromatic hydrocarbons (PAHs) in three native fish species—mullet, sea bream and tonguesole—captured from Kuwait Bay (KB) area and outside the Bay from the Auha area between October 2004 and June 2005. KB has witnessed rapid urban and industrial development since the discovery of oil and is considered to be the most productive area in the region. Whole fish analysis revealed that the lower molecular weight PAHs (pyrene, fluoranthene and phenanthrene) were present in all the three varieties of fish in considerably higher amounts. Other low molecular weight PAHs like acenaphthylene, acenaphthene and anthracene were also present but in lower concentrations. Among the higher molecular weight PAHs, the frequency of detection of benzo(a)anthracene and chrysene was high and were present in high concentrations, whereas Benzo(k)fluoranthene and benzo(a)pyrene were not frequent in detection. The contamination of Σ PAHs was higher in the winter season in mullet and sea bream but in tonguesole a reverse pattern was found. Tonguesole from KB had the highest Σ PAHs suggesting that this bottom dwelling species can be used as an indicator of sediment pollution in the area. The observed seasonality in ∑ PAHs concentration in fish coupled with species difference may be related to difference in metabolic disposition of pollutants and their habitats.     

DISTRIBUTION OF PRIORITY POLYCYCLIC AROMATIC HYDROCARBONS IN THE SEDIMENT OF LAKE BALATON,HUNGARY

The determination of 13 PAH pollutants was carried out on sediment samples collected at 27 sites at the Lake Balaton, Hungary. The aim was to investigate the distribution patterns of PAHs and the correlation of source-sink relationship. Sediment samples were collected from the upper 10 cm and from 20 to 70 cm depth. The dry mass ratio of the fine grain-size fraction (<0.063 mm) and the coarse sand sediments (0.063–500 mm) were analyzed. Principal component analysis (PCA) was performed on the PAH compositional data for 110 samples to estimate the distribution of PAHs in different compartments. The average concentration of PAHs was found as 132 μg/kg dry weight (11–1734 μg/kg) for all sites and depth. Considering the harbors, at some sites, 930–950 μg/kg of total PAHs were obtained. The ratio of phenantrene/anthracene (PHE/AN) and fluoranthene/pyrene (FA/PY) indicated that most of the samples showed pyrogenic origin. It can be established that the upper 10 cm of the sediment is significantly more polluted than the deeper layers. The interim sediment quality guideline (ISQG) values and the probable effect level (PEL) were used to compare our findings with other data. No concentrations of PAHs were found higher than either ISQG and PEL values of samples collected inside of the lake, so the sediment has not been associated with adverse biological effects. However, the maximum concentrations of 7 out of 9 PAH compounds found in samples of harbors were higher than ISOG values but lower than PELs. Analysis of the harbor sediments revealed an elevated amount of contamination probably derived from the fuel of ships.     

IN VITRO INTESTINAL TRANSFER AND METABOLISM OF POLYCYCLIC AROMATIC HYDROCARBONS

Though polycyclic aromatic hydrocarbon (PAH) transfer through intestinal epithelium seems principally governed by transcellular diffusion, other mechanisms may interfere. Several studies suggest a PAH metabolism via CYP450, particularly in liver, but only few data are available regarding intestinal barrier. This in vitro work aimed at studying PAH metabolism and its consequences on the transfer in the intestinal epithelium according to molecule physicochemical properties. It used ¹⁴C-labeled benzo[a]pyrene, pyrene, and phenanthrene. Medium analysis proved a metabolism in intestinal cells for each PAH. Parallel metabolism appeared to play a positive role in the intestinal transfer of PAHs under different forms: ¹⁴C from benzo[a]pyrene, pyrene, and phenanthrene were respectively transferred 26, 4, and 2 times less when cells were incubated with CYP450 inhibitors. Generally speaking, the faster and the higher a PAH crosses intestinal barrier, the less metabolized it will be.     

SAMPLING AND ANALYSIS OF POLYCYCLIC AROMATIC HYDROCARBONS IN URBAN AND RURAL ATMOSPHERES: SPATIAL AND GEOGRAPHICAL VARIATIONS OF CONCENTRATIONS

Atmospheric sampling (gas and particles) of PAHs (naphthalene, acenaphthene, fluorene, anthracene, phenanthrene, fluoranthene, pyrene, benz[a]anthracene, chrysene, benzo[b]fluoranthene, benzo[j]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, benzo[ghi]perylene, dibenz[a,h]anthracene, indeno[1,2,3-cd]pyrene, coronene) on XAD-2 resin (20 g) and glass fiber filters respectively, were performed in 2002 by using Digitel DA80 high-volume samplers equipped with a PM10 head. Samplings were performed in Strasbourg (east of France) and its vicinity (Schiltigheim and Erstein). Sites were chosen to be representative of urban (Strasbourg), suburban (Schiltigheim), and rural (Erstein) conditions. Field campaigns were undertaken simultaneously in urban, and suburban, urban and rural sites during spring and autumn during 4 h at a flow rate of 60 m³/h^?1 which gives a total of 240 m³ · h^?1 of air per sample. The period of sampling varied between 06:00 to 10:00, 11:00 to 15:00, 17:00 to 21:00 in order to evaluate a variation of concentration during automobile traffic between urban, suburban, and rural areas. Gas and particle samples were separately Soxhlet extracted for 12 h with a mixture of CH₂Cl₂/n-hexane (50:50 v/v), concentrated to about 1 mL with a rotary evaporator and finally dried under nitrogen. Dry extracts were dissolved in 1 mL of CH₃CN before analysis. Before use, traps were Soxhlet cleaned for 24 h with the same mixture as used for the extraction. Analysis of each extract was performed by reverse phase HPLC, and fluorescence detection and quantification was done with respect to triphenylene used as internal standard. Results shows that automobile traffic seems to be the main source of PAHs in urban areas whatever the period (autumn and spring) while in autumn other sources, especially coming from combustion, influence the atmospheric contamination by PAHs.     

POLYCYCLIC AROMATIC HYDROCARBONS ANALYZED IN RAINWATER COLLECTED ON TWO SITES IN EAST OF FRANCE (STRASBOURG AND ERSTEIN)

Polycyclic Aromatic Hydrocarbons (naphtalene, acenaphtene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benzo[a]anthracene, chrysene, benzo[j]fluoranthene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, dibenzo[a,h]anthracene, benzo[g,h,i]perylène, indeno[1,2,3-c,d]pyrene and coronene) have been consecutively analyzed in rainwater sampled in Strasbourg (urban site) and Erstein (rural site) between January 2002 and June 2003 and between April 2002 and June 2003 on a weekly basis respectively. For the sampling of rainwater, a wet-only rainwater sampler was used together with an open collector to take the measurements of precipitation.

PAHs in rainwater were extracted by using SPE cartridges and analyzed by HPLC-fluorescence following a method developed in the laboratory.

Mean concentrations of all PAHs (Σ 16 HAPs) varied between 0.15 and 79.60 ng·L^?1 in Erstein, and between 3.70 and 1596.45 ng·L^?1 in Strasbourg. Naphtalene, phenanthrene, fluoranthene, pyrene, chrysene, benzo[j]fluoranthne and benzo[a]pyrene were the most concentrated PAHs analyzed. Benzo[a]pyrene was frequently detected. Seasonal effects were observed with a maximum of concentrations of PAHs during cold periods. Some spatial influences were also reported. The calculation of some PAH ratios show that diesel exhaust could be the main source of PAHs in rainwater on the two sites.     

炼焦过程中多环芳烃与NOx产生的相关性

通过对炼焦过程产生的多环芳烃(PAHs)和NOx浓度进行监测,得到PAHs和NOx的产生规律及其产生的相关性.结果显示,PAHs主要在煤的升温阶段产生,在结焦初期的1 h～3 h产生的多环芳烃最多,整个炼焦过程中的产生量逐渐减少;随炼焦时间延长,NOx浓度先增大后减小,在最初的第4 h～第6 h出现峰值;在炼焦过程前期,PAHs和N0x的产生量呈负相关性,通过指数拟合,得到不同煤种和配煤情况下PAHs与NOx最大产生量的关系式.     

POLYCYCLIC AROMATIC HYDROCARBONS (PAH) IN DANISH SMOKED FISH AND MEAT PRODUCTS

Twenty seven PAH were detected in 45 selected smoked food samples produced in Denmark, including mackerel, herring, trout, small sausages, salami, and bacon. The sum of PAH in smoked meat products ranged from 24 μg/kg for salami to 64 μg/kg in bacon, while those in fish products ranged from 22 μg/kg in smoked mackerel prepared in an electric oven to 1387 μg/kg in herring smoked by direct smoking. The concentration of benzo[a]pyrene for all sample types were below the maximum level of 5 μg/kg for smoked fish and meat set by the European Commission. Results from this survey confirm that the actual level of individual PAH in fish products is dependent on variables such as the type of wood used in the smoking process. Furthermore, the use of the benzo[a]pyrene approach for estimation of the carcinogenicity of PAH in food is confirmed. The Danish intake of benzo[a]pyrene from these smoked products is 2 to 4 ng/person/day.     

POLYCYCLIC AROMATIC HYDROCARBONS BIOACCUMULATION AND BIOTRANSFORMATION PRODUCTS IN TROUT EXPOSED THROUGH FOOD PELLETS

Polycyclic aromatic hydrocarbons (PAHs) were previously measured in whole small finfish (< 30 cm) or in the internal organs relative to the rest of tissues, as well as in muscle, liver, and gonads of larger finfish, collected offshore in the Northwest Atlantic. Alkylated naphthalenes (NA) were more abundant than phenanthrenes (PA), while fluoranthene (FL), pyrene (PY), and chrysene (CH) were also detected in some cases. Bioaccumulation pointed to uptake by respiration and, probably by a dietary contribution, especially for benthic species. Therefore, speckled trout were exposed to PA, FL, and PY through food and the parent PAH and their respective metabolites were analyzed. Trout maintained at 10°C were fed daily for 10 weeks with pellets spiked with 0.33–0.38 μg of each PAH per g fish. Muscle, internal organs, and bile of fish were analyzed by HPLC every 2 weeks, for up to 14 weeks. The concentration of PA was always higher than that of FL. No phase I or phase II metabolites were detected for either compound, even in the bile. Concentrations and total tissue burdens were higher in the internal organs than in the muscle for PA and FL. The highest levels of PA equivalent to 5 days' feeding were present in internal organs on week 10. Levels of PY were lower than levels of FL in internal organs and muscle. The amounts of PY-glucuronide in whole gall bladder bile were higher than amounts of PY in any whole compartment. PY-glucuronide was also detected in internal organs. Comparison will be made to a short-term exposure of winter flounder to 5 μg/g of the same three PAHs.     

SEMIPERMEABLE MEMBRANE DEVICE-AVAILABILITY OF POLYCYCLIC AROMATIC HYDROCARBONS IN RIVER WATERS AND WASTEWATER TREATMENT PLANT EFFLUENTS

River waters and wastewater treatment plant effluents contain hydrophobic organic compounds (HOCs) such as polycyclic aromatic hydrocarbons (PAHs) which are persistent, bioaccumulative, and dangerous for the environment. The biological risk assessment of HOCs requires the estimation of their bioavailable fraction in addition to the total contamination of the media. The bioavailability of HOCs depends on the characteristics of the aquatic environments. In particular, the presence of organic matter (OM) usually reduces the bioavailability of HOCs by trapping them and preventing them from crossing biological membranes. The semipermeable membrane device (SPMD) technique is used to evaluate bioavailable fractions of HOCs. We tested the influence of aquatic and more particularly OM characteristics on the SPMD-availability of PAHs, in several river waters (up and downstream a large town) and in wastewater treatment plant effluents. Thirteen priority PAHs were analyzed in total water and in SPMDs. Aquatic environments were characterized for their pH, ionic strength, temperature, chlorophyll A, and suspended solids contents. Total and dissolved OMs were characterized for aromaticity, biodegradability, molecular weight, and hydrophobicity. The total PAH contamination increased downstream the river; wastewater effluents were proven to be a source of SPMD-available PAHs. We attempted to establish relationships between the characteristics of organic matter and the SPMD-availability in order to initiate an aquatic environment typology: The SPMD-availability was negatively related to dissolved OM molecular weight and aromaticity, and positively related to biodegradability.     

POLYCYCLIC AROMATIC HYDROCARBONS IN PRODUCTS OF A BEET SUGAR FACTORY IN VOJVODINA: LEVELS AND INTAKES

The levels of 16 EPA polycyclic aromatic hydrocarbons (PAHs) were investigated in samples of sugar beets and their products representative for a beet sugar factory located in the central part of Vojvodina, the main agricultural region in Serbia. The sum of the detected PAHs ranged from 51 pg g ^?1 ww for molasses to 391 pg g ^?1 ww for dried sugar beet pulp. The concentration of benzo(a)pyrene (BaP) for all sample types was about or less than 100 pg g ^?1 ww, which is far less than the existing Serbian and EU tolerances set for some foodstuffs. The Serbian intake of BaP via total sugar consumption that ranged from 70–85 g per capita day ^?1 , was assessed to be from 0.029 to 0.035 ng kg ^?1 b.w. day ^?1 . Furthermore, the toxic equivalency factor (TEF) approach was used to estimate the carcinogenicity of PAH mixture found in analyzed samples.     

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).     

EFFECTS OF FLOW RATE AND TEMPERATURE ON THE DISSOLUTION OF POLYCYCLIC AROMATIC HYDROCARBONS TRANSFERRING FROM A NONAQUEOUS PHASE LIQUID TO NONIONIC SURFACTANT SOLUTIONS

The effects of flow rate and temperature on the dissolution of two polycyclic aromatic hydrocarbon (PAH) compounds, naphthalene and phenanthrene, transferring from a synthesized nonaqueous phase liquid (NAPL) comprised of hexadecane and the 2 PAHs into different nonionic surfactant solutions were investigated using a reactor with a spinning cell. The variation of the flow rate was possible by changing the angular velocity of the spinning cell. The flow rate generally increased the values of the mass transfer coefficients and the rates of mass transferred for both aromatics in the absence and presence of a surfactant in the aqueous phase. In comparison to the pure aqueous solution the results suggest that the addition of a surfactant at all doses investigated enhanced the rates of mass transfer for both PAHs. As the temperature increased the rates of mass transfer for both PAHs in the solutions of surfactants increased. The increase in the temperature has a much greater effect on the rates of mass transfer for both PAHs in solutions of the surfactant Triton X-100 than in Brij 35. In solutions of the surfactant Triton X-100 a decrease in the mass transfer coefficient for both PAHs with surfactant concentration was observed for the temperatures investigated.     

DETERMINATION OF POLYCYCLIC AROMATIC HYDROCARBONS (PAHs) IN SEDIMENTS AND BENTHOS COLLECTED ON THE COAST OF CHIBA

Eight polycyclic aromatic hydrocarbons (PAHs) including benzo[a]pyrene were analyzed in sediment and benthos collected on the coast of Chiba Prefecture in Japan by gas chromatography-mass spectrometry (GC/MS). The total concentration of the PAHs ranged from 8 to 18 μ g/kg-dry in the sediments and from 36 to 59 μ g/kg-wet in the benthos, Mactra quadrangularis, Scoletoma nipponica, and Arenicola basiliensis. The PAH composition in the sediments and the benthos was similar at four sampling points and dominated by phenanthrene (Phe), fluoranthene (Flu), and pyrene (Pyr). The ratios of abundance of Flu to that of Pyr, Flu/Pyr, and of Phe/anthracene suggest that the PAHs in the benthos are derived from the combustion of fossil fuels. The ratio, R, of the PAH concentration in the benthos to that in the sediment is 2.0 for Scoletoma nipponica and 1.8 for Arenicola basiliensis in average, indicating that the bioaccumulation is not significant in the benthos. However, the R value for perylene in Scoletoma nipponica was 3.7 times as large as the average.     

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.     

GAS-PARTICLE PARTITIONING OF POLYCYCLIC AROMATIC HYDROCARBONS DURING THE SPRING AND SUMMER IN A SUBURBAN SITE NEAR MAJOR TRAFFIC ARTERIES

Concentrations of atmospheric polycyclic aromatic hydrocarbons were measured in a suburban site near major traffic arteries during the period April-August 2006. Total suspended particulate during the sampling period was 65.3 ± 33.9 μ g m^?3. Total PAH concentrations were 63.5 ± 20.1 ng m^?3 in the gaseous phase and 1.4 ± 0.3 ng m^?3 in the particulate phase. Observed concentrations were comparable with previously measured values reported in the literature for urban and suburban sites with a high anthropic influence. PAH concentration diagnostic ratios indicate that, during the spring and summer seasons, vehicular emission was the main source of atmospheric PAHs.

Gas/particle partitioning coefficients K _P were well correlated with both the sub-cooled liquid vapor pressures p _L ⁰ and the octanol-air partition coefficients K _OA . Measured K _P values were in a good agreement with K _P values predicted by applying a literature model, which takes into account both adsorption onto black carbon and absorption into the organic matter.     

SIMULTANEOUS GC/MS ANALYSIS OF POLYCYCLIC AROMATIC HYDROCARBONS AND THEIR NITRATED DERIVATIVES IN ATMOSPHERIC PARTICULATE MATTER FROM WORKPLACES

Abstract

PAH are routinely analyzed using HPLC/FD. This technique is unsuitable for analyzing NPAH. This study aims at developing a reliable method, using GC/MS, and applying this technique to actual samples from small volumes of atmospheric particulate matter from workplaces. Mixtures of PAH and NPAH were separated by GC/MS and detected by electronic impact (EI) or negative ion chemical ionization (NICI). Analyses on twelve actual samples were thus carried out by sampling a small volume of atmosphere (≈0.5 m ³ ) from five different industrial workplaces. Samples displayed wide differences from one industrial workplace to another, and this can be explained by the specific methods applied. The PAH and NPAH concentrations also varied with time in the same industrial workplace. NPAH concentrations were not correlated with PAH concentrations, underscoring the complex chemical mechanisms involved in NPAH formation. PAH and NPAH formation appeared to be dependent on both industrial activities and uncontrolled physicochemical conditions.     

H2AX,MDM2 AND P53 PHOSPHORYLATION ARE DIFFERENTLY AFFECTED BY BAY- AND FJORD-REGION DIOL EPOXIDES DERIVED FROM CARCINOGENIC POLYCYCLIC AROMATIC HYDROCARBONS

The human lung cancer cell line A549 was exposed to diol epoxides (DEs) and the effect on DNA damage signaling proteins was studied. The DEs used were derived from the bay-region PAHs chrysene; CDE and dibenz[a,h]anthracene; DBADE, or the fjord-region PAHs benzo[c]chrysene; B[c]CDE, benzo[g]chrysene; B[g]CDE and benzo[c]phenanthrene; B[c]PhDE. All DEs induced a rapid response on Mdm2, p53 and histone H2AX phosphorylation, where Mdm2 was the most sensitive marker of DNA damage. Fjord-region DEs induced a stronger and more persistent effect on the proteins studied than the bay-region DEs. This variance is likely to reflect differences in adduct recognition and handling by nucleotide excision repair. The stimulating effect of DEs on histone H2AX phosphorylation demonstrated that, in addition to DNA strand breaks and UV-induced photoproducts, stable and bulky DNA-adducts also possess this capacity.     

CHARACTERIZATION AND COMPARISON OF SPECIATED ATMOSPHERIC CARBONACEOUS PARTICULATES AND THEIR POLYCYCLIC AROMATIC HYDROCARBON CONTENTS IN THE CONTEXT OF THE PASO DEL NORTE AIRSHED ALONG THE U.S.-MEXICO BORDER

Carbonaceous particulate matter (PM) was collected by both thermal precipitation and glass fiber filters from specific combustion sources and examined by transmission electron microscopy (TEM) and field emission scanning electron microscopy (FESEM). PM from various natural gas burner combustion regimes (NGPM), burning tires (TPM), a heavy duty diesel truck (DPM), wood burning (WPM), candle burning (CPM), along with commercial black carbon (BC) powder and multiwall carbon nanotube (MWCNT) aggregates material exhibited similarities in PM microstructure, and average primary spherule diameters. The spherule structures consisted of curved graphene fragments and intercalated polycyclic aromatic hydrocarbons (PAH). PAH concentrations were measured and compared for these PMs, including PAH diagnostic ratios. An analysis of PAH carcinogenicity either as a carcinogenicity index or a potency equivalency factor from literature data indicated that only the TPM PAH content would pose any significant long term, carcinogenicity threat.     

LEAVES OF NERIUM OLEANDER L. AS BIOACCUMULATORS OF POLYCYCLIC AROMATIC HYDROCARBONS (PAH) IN THE AIR OF PALERMO (ITALY): EXTRACTION AND GC-MS ANALYSIS,DISTRIBUTION AND SOURCES

Polycyclic Aromatic Hydrocarbons (PAH) were determined in the leaves of Nerium oleander L. an evergreen plant that occurs widely in both urban and rural areas, to monitor the degree of pollution in the urban area of Palermo (Italy) compared to remote areas. Twenty sites (urban roadside, urban, urban park, suburban and rural) in and around Palermo city were investigated.

The purpose of this research was to investigate concentration levels and distribution patterns and relate them to possible sources. Analysis of 19 PAH was performed by gas chromatography/mass spectrometry (GCMS) using selected ion monitoring (SIM). The total amount of PAH ranged from 10 to 166 μg/Kg d.w.

Each source gives rise to a characteristic PAH pattern, and it is therefore possible to get access to the processes that generate the compounds. To this aim, the recommended as priority pollutants by the Environmental Protection Agency (EPA), perylene and three additional alkylated compounds were analyzed.

Positive correlations were found between total PAH content of the leaves with CO, benzene and particulate levels measured in air of Palermo.