Ecological risk assessment of polycyclic aromatic hydrocarbons (PAHs) in the water from a large Chinese lake based on multiple indicators

In the surface water of Lake Chaohu, China, the concentrations of 16 priority polycyclic aromatic hydrocarbons (PAHs) were measured by gas chromatograph–mass spectrometer (GC–MS). Based on the species sensitivity distribution (SSD) model and the probabilistic risk assessment (PRA) model, the indicators were calculated to assess the potential ecological risk of the individual and of multiple congeners of PAHs and their probabilities. The results revealed that the average residual level of the total PAHs (PAH₁₆) in the water ranged from 95.2 to 370.1 ng/L, with a mean value 181.5 ± 70.8 ng/L. The PAH content in the water was dominated by the low-molecular-weight congeners. The multi-substance potentially affected fractions (msPAFs) of the studied PAHs obtained by the SSD model varied from 0.29% (site B3) to 1.58% (site B6), with an average of 0.51 ± 0.34%. The average of the msPAFs (0.93%) for the inflow rivers was greater than that for the western (0.42%) and eastern (0.34%) parts of the lake. The greatest ecological risk probability calculated by the PRA model was found for Pyr (1.55%), followed by Ant (7.07 × 10⁻²%), Fla (2.21 × 10⁻²%), Phe (9.25 × 10⁻⁶%), Nap (1.01 × 10⁻⁵%), Flo (1.16 × 10⁻¹⁴%) and Ace (2.86 × 10⁻¹⁶%). The same order of ecological risks calculated by the two models was found for the studied PAH compounds. The toxicity data might be the primary source of the ecological risk uncertainties, as indicated by the greater values of coefficients of variation (CV) for the toxicity. This study concluded that the combinations of multiple indicators based on the SSD and PRA models for the ecological risk assessment are necessary to provide more general information on the spatial variations and the probabilities of potential ecological risks of the individual and multiple congeners of PAHs.     

Distribution,sources, and health risk assessment of polycyclic aromatic hydrocarbons in dust from urban environment in the Niger Delta,Nigeria

The concentrations of the 16 U.S. Environmental Protection Agency polycyclic aromatic hydrocarbons (PAHs) were measured in urban street dust with a view to understanding the potential risk to urban residents exposed to street dust, sources, and distribution of the PAHs. Gas chromatography–mass spectrometry was used to measure the concentrations of the PAHs after ultra-sonication with hexane/dichloromethane and clean up. The total concentrations of the ?16 PAHs in the urban street dust from Warri and its environs ranged from 165.1 to 1012 µg kg^?1. The isomeric ratios and the PCA indicated that combustion of petroleum and biomass are the major sources of PAHs in Warri and its environs. The total BaP carcinogenic and mutagenic potency concentrations (?BaP_TEQ and ?BaP_MEQ) were in the range of 0.03 to 219 µg kg^?1 and 0.52 to 182 µg kg^?1, respectively. The incremental life cancer risk from exposure of the residents of Warri and its environs ranged from 4.07 × 10^?7 to 3.11 × 10^?3 and 2.13 × 10^?7 to 1.49 × 10^?3 for the children and adults, respectively, which were higher than the baseline value of acceptable risk of 10^?6 (i.e., one case per million people).     

Distribution Characteristics and Risk Assessments of PAHs in Fish from Lake Taihu,China

The concentrations of PAHs in four species of fish (Common carp, Crucian carp, Bighead carp, and Topmouth culter) from Lake Taihu were tested, and the human health risks of PAHs by fish consumption were evaluated. Results showed that concentrations of PAHs in fish from Lake Taihu were 52.5–247.6 ng/g wet weight (ww), and the BaP equivalent concentrations of total PAHs (B[a]P_eq) were 0.2–0.6 ng/g ww, which were less than the screening value of 2.6 ng/g wet for human consumption. The concentration sequences of PAHs in fish from Lake Taihu from high to low were Bighead carp > Crucian carp > Common carp > Topmouth culter. The human health risk level of PAHs by fish consumption was 5.8 ± 2.5 × 10^?6, which was less than the maximum acceptable risk level of 1 × 10^?5 for human health set by the U.S. Environmental Protection Agency. The tissue residue guideline (TRG) of PAHs for protecting aquatic wildlife was 1.3 mg/kg diet ww, which was higher than the concentrations of PAHs in fish from Lake Taihu. The results indicated that fish consumption from Lake Taihu would not cause health risk or harmful effects on wildlife that consume aquatic biota.     

Contamination,source identification,and risk assessment of polycyclic aromatic hydrocarbons in agricultural soils around a typical coking plant in Shandong,China

Coking is one of the most important emission sources of polycyclic aromatic hydrocarbons (PAHs) in China. Investigation of the contamination, distribution, and sources of PAHs in agricultural soils around Rong Xin coking plant, China, was conducted, and the potential human health risks were addressed. The total concentration of the 16 PAHs (∑₁₆PAHs) on the United States Environmental Protection Agency priority list had a range from 1774 to 4621 µg/kg (mean 3016 µg/kg). Meanwhile, seven carcinogenic PAHs (∑PAH_7c) owned the total concentrations of 684–2105 µg/kg, and they had the benzo[a]pyrene equivalent (BaP_eq) concentrations at 139.616–1672.850 µg/kg. All soil samples were dominated by PAHs with two to four rings. Data analyses for the potential sources of PAHs showed that the PAHs in soils were principally from pyrogenic sources. Ecological risk assessment of soil PAHs showed that the BaP_eq concentrations of ∑PAH_7c accounted for 99% of the total ∑₁₆PAHs, being a major carcinogenic contributors of ∑₁₆PAHs. Higher levels of PAHs and higher total BaP_eq concentrations in this study indicate a potential carcinogenic risk for humans. Therefore, long-term exposure to coking plants may increase the PAH concentrations in the environment and further raise a potential risk to human health.     

Bioaccessibility-Based Risk Assessment of PAHs in Soils from Sites of Different Anthropogenic Activities in Lagos,Nigeria Using the Fed Organic Estimation Human Simulation Test Method

The aim of this study was to carry out a bioaccessibility-based risk assessment of polycyclic aromatic hydrocarbons (PAHs) in soils from sites of different anthropogenic activities in Lagos, Nigeria. Using an in vitro gastrointestinal model—Fed Organic Estimation Human Simulation Test method (FOREShT), the concentration of bioaccessible 16 priority US Environmental Protection Agency (USEPA) PAHs in soils were determined. Total concentration of 16 priority USEPA PAHs was also determined. The concentration range was 702–253,922 ng g^?1 and 92–760 ng g^?1 for total and bioaccessible PAHs, respectively. For persons involved with activities at these sites no health risks were observed, based on bioaccessibility values of PAHs. Mean daily intake of PAHs from these soils were below the oral mean daily intake threshold for PAHs in food. Also, overall estimated theoretical cancer risk (2.5 × 10^?09, 6.5 × 10^?07, 5.5 × 10^?10, 2.7 × 10^?09, 6.5 × 10^?10, 9.5 × 10^?10, 2.0 × 10^?09, and 4.1 × 10^?07 for the eight sites based on their bioaccessible concentration) for exposure to PAHs in surface soils were below the health guidelines for extreme (1 × 10^?04) and normal (1 × 10^?06) exposures.     

长江口南支表层沉积物中多环芳烃分布特征及生态风险

2008年5月和8月先后2次采集长江口南支表层沉积物样品,采用高效液相色谱进行多环芳烃测定,研究其分布、来源与生态风险。结果表明:长江口南支表层沉积物中PAHs总量在8.9~312.2ng.g-1;PAHs组成以芘、菲、苯并[b]荧蒽、苯并[a]蒽、苯并[a]芘为主,各站芘的含量均最高,本研究PAHs总含量与长江口、黄河口和鸭绿江口近期的调查数据相近,但明显低于珠江口和闽江口数据,以及长江口潮滩沉积物中PAHs数据;PAHs环数组成以中、高环为主,表明长江口南支PAHs主要来源于相对高温条件下不完全燃烧过程。采用平均效应中值商法评价长江口南支PAHs生态风险结果表明,调查区域PAHs产生生态风险的概率较小(<10%)。     

Estimation of Toxicity Equivalency and Probabilistic Health Risk on Lifetime Daily Intake of Polycyclic Aromatic Hydrocarbons from Urban Residential Soils

In this study, toxicity equivalents and health risks, based on concentration of 16 priority polycyclic aromatic hydrocarbons (PAHs) in urban residential soils were estimated for the human population in Gwalior, India. Benzo(a)pyrene total potency equivalents (BaP TPE) were estimated for assessment of human health risk from direct contact with PAH-contaminated soil. Potential risk to contaminated groundwater from leaching of carcinogenic PAHs was assessed by estimating the index of additive cancer risk (IACR). On the basis of lifetime average daily intake of 16 PAHs through ingestion of PAH-contaminated soils, lifetime cancer risk to human adults and children was estimated. The concentration of probable human carcinogenic PAHs in soils accounted for 38% of ∑16PAHs. BaP TPE and index of additive cancer risk (IACR) were lower than guideline values of 0.6 mg kg^?1 and <1, respectively. Estimated lifetime average daily intakes of PAHs via soil ingestion were lower than recommended dose. However, the ILCR for human adults was within acceptable limits recommended by regulatory agencies, but may need action for children in Gwalior, India.     

Evaluation of PAHs concentration and cancer risk assessment on human health in a roadside soil: A case study

Abstract

An explanatory study was carried out to divulge the sources, contamination level of different classes of Polycyclic Aromatic Hydrocarbons (PAHs) distribution and the impact of vehicular traffic on the roadside soil by assessing incremental lifetime cancer risk at each site to understand the potential health risk of nearby residents along the National Highway-2 Delhi–Kolkata India. Comparison of the cancer risk assessment was performed using Monte Carlo simulation for the entire study area. The results revealed 90% cancer risk value of 6.40?×?10^?5 and 6.5?×?10^?5 for children and adults, respectively, whereas, without simulation the Total Cancer Risk (TCR) for adults was 6.925?×?10^?5 and 6.220?×?10^?5 for children, observed maximum at the location (S5). The dilemma of risk assessment indicating profoundly contaminated soil. Comparison of PAHs concentration with the background values of PAHs ranged from 1.478 to 27.493?mg kg^?1. The (IP/BgP) ratio specified that the PAHs content of the highway roadside sample is preponderate by diesel vehicle emission, biomass combustion and coal combustion. The study clearly revealed and advocated the influence of organic and inorganic pollution, which aggravates and causes health issues to the nearby inhabitants. This study could also be advantageous to similar consequences seen elsewhere in the world.     

Pollution,sources, and ecological-health risks of polycyclic aromatic hydrocarbons in coastal waters along coastline of China

Abstract

This study investigated the distribution, sources, and potential risks of polycyclic aromatic hydrocarbons (PAHs) in coastal waters along over 18,000?km of coastline in China. Concentrations of PAHs in coastal waters ranged from 141.99 to 717.72?ng/L. Approximately 84.38% of sampling sites were determined at moderate PAH pollution level. PAHs in coastal waters at most of sampling sites mainly originated from combustion based on characteristic ratios of PAHs. Ecological risks posed by PAHs in coastal waters were evaluated as high level at 59.38% of sampling sites and moderate level at 40.63% of sampling sites although toxic equivalent quotients of PAHs only ranged from 2.86 to 126.52?ng/L benzo[a]pyrene that was not detected at all sampling sites. Maximal cancer risk/hazard quotient of total PAHs in coastal waters for adults and children reached 6.34?×?10^?4/5.85?×?10^?2 and 2.25?×?10^?3/7.72?×?10^?2, respectively. PAHs exerted high cancer risks for children at 31.25% of sampling sites. Health risks posed by PAHs in coastal waters of this study were higher than those of Japan, Belgium, Greece, Italy, Spain, USA, and Australia, but much lower than those of Singapore, Iran, Brazil, and Egypt. These findings indicate that PAH pollution has become a crucial stress affecting the sustainable development of coastal regions.     

PAHs and their Carcinogenic Potencies in Diesel Fuel and Diesel Generator Exhaust

The PAH profile was characterized in diesel fuel samples collected from different service stations in Agra (India) by using a gas chromatograph equipped with a flame ionization detector (FID). The low molecular weight PAHs were predominant, ranging from 4.4 × 10² to 1.7 × 10³ mg l^{? 1} in fuel. Exhaust emissions from a diesel generator and a four-stroke engine (Skoda) powered by these fuels were monitored by a stack sampler and quantified for PAHs. The high molecular weight PAHs (DbA+IP, BghiP, and BaP, BbF+BkF) were the dominant PAHs in exhaust emissions. Differences in PAH emission factors for the two engines were found and these differences could be related to the combustion conditions affecting the temperature of flue gas. Emission factors and output/input ratio for individual PAHs suggest that the low molecular weight compounds in the fuel contribute to pyrosynthesis of high molecular weight in exhaust. Unburnt fuel partially contributes to low molecular weight PAHs in exhaust. Further, the relative carcinogenic contributions of each compound in the fuel and exhaust were calculated using the TEF approach. DbA + IP and BaP were significant contributors to the carcinogenicity of the PAH mixture in the exhaust.     

Effect of Exposure Time,Contamination Level,and Type of PAH Compound on Biodegradation Capacity of Mangrove Sediment

Mangrove sediment had high natural attenuation potential with more than 50% of total PAHs being removed within 15 days. The efficiency in degrading PAHs varied with the declining order of phenanthrene (Phe), fluoranthene (Fla), and pyrene (Pyr). The Most Probable Number (MPN) of PAH-degrading bacteria in the PAH-contaminated slurries was 2 to 4 orders of magnitude higher than that in the non-contaminated mangrove slurries. The biodegradation ability of the indigenous microbial community in mangrove sediment slurry was significantly increased after exposure to polycyclic aromatic hydrocarbons. Such enhancement effect was dependent on the level and time of exposure, as well as the types of PAH compounds. The lowest contamination level of 3 mg kg^?1 was effective in promoting the degradation of Phe and Fla after seven days, but the enhancement effect for Pyr degradation was only found in the slurries exposed to contamination levels of 9 mg kg^?1 for 30 days, suggesting a threshold concentration of PAHs to stimulate growth and activity of pyrene-degrading bacteria. The contamination level higher than the threshold concentration did not lead to more degradation. The present study provides insights into the natural attenuation of PAH-contaminated mangrove sediments.     

Degradation of polyaromatic hydrocarbons by Burkholderia cepacia 2A-12

A new strain of bacterium degrading polyaromatic hydrocarbons (PAHs), Burkholderia cepacia 2A-12, was isolated from oil-contaminated soil. Of three PAHs, the isolated strain could utilize naphthalene (Nap) and phenanthrene (Phe) as a sole carbon source but not pyrene (Pyr). However, the strain could degrade Pyr when a cosubstrate such as yeast extract (YE) was supplemented. The PAH degradation rate of the strain was enhanced by the addition of other organic materials such as YE, peptone, glucose, and sucrose. YE was a particularly effective additive in stimulating cell growth as well as PAH degradation. When 1 g YE l^–1, an optimum concentration, was supplemented into the basal salt medium (BSM) with 215 mg Phe l^–1, the specific growth rate (0.30 h^–1) and Phe-degrading rate (29.6 mol l^–1 h^–1) were enhanced approximately ten and three times more than those obtained in the BSM with 215 mg Phe l^–1, respectively. Both cell growth and PAH degradation rates were increased with increasing Phe and Pyr concentrations, and B. cepacia 2A-12 had a tolerance against Phe and Pyr toxicity at the high concentration of 730–760 mg l^–1. Through kinetic analysis, the maximum specific growth rate ( _max) and PAH degrading rate ( _max) for Phe were obtained as 0.39 h^–1 and 300 mol l^–1 h^–1, respectively. Also, _max and _max for Pyr were 0.27 h^–1 and 52 mol l^–1 h^–1, respectively. B. cepacia 2A-12 could simultaneously degrade crude oil as well as PAHs, indicating that this bacterium is very useful for the removal of oils and PAHs contaminants.     

Distribution,Levels, and Risk Assessment of Polycyclic Aromatic Hydrocarbons (PAHs) in Singed Cattle Hide

Human beings are exposed to polycyclic aromatic hydrocarbons (PAHs) from various occupational, environmental, and dietary sources. The study was carried out in the Cape Coast Metropolis of Ghana to assess the levels of PAHs in treated and untreated cattle hide and the associated health risks thereof. Treated cattle hide (wele) is one of the most well-patronized meat products in Ghana. A total of 90, treated (n = 36), untreated (n = 36), and control (n = 18) cattle hide samples were treated and analyzed using a gas chromatography flame ionization detection (GC/FID) technique. The total PAH concentration in the treated cattle hide ranged from 5.9 μg/kg naphthalene to 719.9 μg/kg benzo[b]fluoranthene. The total PAHs in untreated hide ranged from 57.6 μg/kg naphthalene to 19840.9 μg/kg benzo[b]fluoranthene. The amount of PAHs in the control hide, however, ranged from non-detectable for many of the PAHs to 0.5 μg/kg for fluorene. The carcinogenic risk value associated with the consumption of treated hide in children ranged between 1.0 × 10^?3 and 9.4 × 10^?3 whereas that of adults ranged between 1.9 × 10^?4 and 2.1 × 10^?5. This implies that the continuous consumption of heavily burnt cattle hide may not exempt the consumers from all the possible health cases associated with PAHs.     

Optimization of PAHs Oxidation from a Concentrate of Soil Attrition Using Potassium Permanganate

The treatment of soils contaminated with organic compounds, such as polycyclic aromatic hydrocarbons (PAHs), by attrition produced large amounts of highly concentrated attrition sludge (PAH – attrition concentrate – PAC). This paper studied the performance of an oxidation process using potassium permanganate (KMnO₄) to degrade PAHs that were initially present in attrition concentrates. The influence of operating conditions (temperature, concentration of KMnO₄ and reaction time) was studied, and these parameters were optimized using a response surface methodology (RSM). The results showed that the temperature and the reaction time had a significant and positive effect on the degradation of PAHs for the experimental domain studied (temperature between 20 and 60°C and reaction time between 1 and 7 h). The interaction between the temperature and the concentration of KMnO₄ significantly influenced the degradation of the PAHs. The temperature and the concentration of KMnO₄ were the main parameters that influenced the degradation of both phenanthrene (Phe) and benzo [a] pyrene (BaP). For benzo [a] anthracene (BaA), the temperature was the most influential factor. According to our results, the optimal conditions were defined as [KMnO₄] = 0.4 M for 5.5 h at 60°C. These optimal conditions led to degradations of 42.9%, 40.8%, 41.0% and 46.0% of the total PAHs, Phe, BaA and BaP, respectively.     

Immunotoxic effect of Benzo[α]Pyrene and chrysene in juvenile white shrimp Litopenaeus vannamei

The effects of benzo(a)pyrene (Bap) (0.03, 0.3 and 3 μg L^?1) and chrysene (CHR) (0.3, 2.1 and 14.7 μg L^?1) on the function of the immune system of juvenile white shrimp Litopenaeus vannamei were determined under laboratory conditions. This included the total hemocyte count (THC) in the hemolymph, phagocytic activityand pro-phenoloxidase (pro-PO) activity of the hemocyte, phenoloxidase (PO) activity, α₂-macroglobulin (α₂-M) activity, bacteriolytic activity and antibacterial activity in the hemolymph. The results showed that BaP and CHR could inhibit the immune function of L. vannamei significantly under high concentration BaP and CHR exposure. The results of this study indicated that the immunotoxicity of PAHs in a descending order was BaP>CHR. Moreover, the results indicated the THC in hemolymph, pro-PO activity and phagocytic activity of hemocyte, and bacteriolytic activity in hemolymphcould be used as potentially suitable biomarkersfor early warning indication of PAHs toxicity, this could provide useful information for toxic risk assessment of environmental pollutants.     

Human health risk assessment of trace elements in shallow groundwater of the Linhuan coal-mining district,Northern Anhui Province,China

Enrichment of trace elements in groundwater poses considerable risks to human health. The concentrations of seven trace elements (Cr, Mn, Ni, Cu, Zn, Cd, and Pb) in 34 samples of shallow groundwater from the study area were estimated. We assessed the concentrations of the trace elements and health risks with statistical analysis and the US Environment Protection Agency (USEPA) model. The results showed that the mean concentrations of trace elements decreased as follows: Mn > Zn > Ni > Cr > Cu > Cd > Pb. Apart from Mn at one sampling point, the concentrations of all trace elements were below the guideline values of the World Health Organization for drinking water. Correlation and cluster analysis indicated that the trace elements fell into groups, with Ni and Cu in one group, and Mn, Zn, and Cd in another, which suggested that the trace elements grouped together had similar sources. The total non-carcinogenic risk values ranged from 8.52 × 10^?4 to 1.27 × 10^?1. The total carcinogenic risk caused by Cr and Cd averaged 1.62 × 10^?6, which exceeded the acceptable level of 1 × 10^?6 recommended by the USEPA. The carcinogenic risk of Cr accounted for 75.93% of R_total.     

Isolation and characterization of pyrene and benzo[a]pyrene-degrading Klebsiella pneumonia PL1 and its potential use in bioremediation

Polycyclic aromatic hydrocarbons (PAHs), which are hard to degrade, are the main pollutants in the environment. Degradation of PAHs in the environment is becoming more necessary and urgent. In the current study, strain PL1 with degradation capability of pyrene (PYR) and benzo[a]pyrene (BaP) was isolated from soil and identified as Klebsiella pneumoniae by morphological and physiological characteristics as well as 16S rDNA sequence. With the presence of 20 mg L^?1 PYR and 10 mg L^?1 BaP in solution, the strain PL1 could degrade 63.4 % of PYR and 55.8 % of BaP in 10 days, respectively. The order of biodegradation of strain PL1 was pH 7.0?>?pH 8.0?>?pH 10.0?>?pH 6.0?>?pH 5.0. Strain PL1 degradation ability varied in different soil. The half-life of PYR in soil was respectively 16.9, 24.9, and 88.9 days in paddy soil, red soil, and fluvo-aquic soil by PL1 degradation; however, the half-lives of BaP were respectively 9.5, 9.5, and 34.0 days in paddy soil, red soil, and fluvo-aquic soil by PL1 degradation. The results demonstrate that the degradation capability on PYR and BaP by PL1 in paddy soil was relatively good, and K. pneumoniae PL1 was the new degradation bacterium of PYR and BaP. K. pneumoniae PL1 has potential application in PAH bioremediation.     

Concentration,Distribution, Source,and Risk Assessment of PAHs and Heavy Metals in Surface Water from the Three Gorges Reservoir,China

Fifteen polycyclic aromatic hydrocarbons (PAHs) and heavy metals (Cr, Ni, As, Cd, Pb, and Hg) were quantified in 19 surface water sites of the Three Gorges Reservoir, China. The total concentrations of 15 PAHs and six heavy metals in the 19 sample sites ranged from 130.8 ng L^?1 to 227.5 ng L^?1 and 3.2 μg L^?1 to 6.0 μg L^?1, respectively. The mean concentration of As was the highest among the six heavy metals (2.1 ± 0.3 μg L^?1), followed by Cr (0.5 ± 0.3 μg L^?1), Ni (1.3 ± 0.1 μg L^?1), Cd (0.2 ± 0.01 μg L^?1), Pb (0.07 ± 0.08 μ g L^?1) and Hg (0.05 ± 0.08 μg L^?1). The isomer ratio results suggest that PAHs at most sites were mainly from petroleum combustion, while coal and biomass combustion was the main source at sites 1, 2, 6, 7, 9, 14, and 17. Based on principal component analysis, the main source of heavy metals was anthropogenic activities and weathering of bedrocks. Depending on characteristic of RQ_(NCs) ≥ 1 and RQ_(MPCs) < 1, BaA showed higher potential ecological risk than other PAHs, therefore, all sampling site needed to be paid much more attention, included some remedial actions. Meanwhile, after assessing human health risk of heavy metal, it was unlikely to experience adverse health effects, even exposing through more pathways and six kinds of heavy metals simultaneously.     

Probabilistic Risk Assessment of Polycyclic Aromatic Hydrocarbons (PAHs) in Produced Water

The produced water extracted during oil and gas production includes formation water, injected water, small volumes of condensed water, and any chemical added during the oil/water separation process. Produced water contains both organic and inorganic constituents, and several studies have been conducted in the past to assess their risk. The toxicity and persistence of polycyclic aromatic hydrocarbons (PAHs) in produced water is of particular environmental concern, but there are very few studies on human health risk assessment from PAHs of produced water. This article summarizes the results of a conservative human health risk assessment approach for PAHs in produced water discharges to the marine environment. Due to the absence of available toxicity data for PAHs, the cancer slope factors were determined by using the relative potency factors (RPF) and Toxicity Equivalency Factors (TEF). Using the concentration distribution factors, the maximum cancer risks to humans were predicted in the range of 4.07 × 10^?7 to 2.95 × 10^?6. The 95th-percentile values show that the risks are well within the acceptable limits.     

PAH contamination in road dust from a moderate city in North China: The significant role of traffic emission

To investigate the contamination level, distribution, possible source, and human exposure risk of polycyclic aromatic hydrocarbons (PAHs) in the urban traffic environment, 15 PAHs were measured in 34 road dust samples (particle size < 25 μm) collected from three grades of roads and park paths in Xinxiang, China. ΣPAHs concentrations ranged from 311 to 21200 ng g^?1, with a mean of 5890 ng g^?1 and decreased in the following order: main roads (7650 ng g^?1) > collector streets (7410 ng g^?1) > bypasses (2970 ng g^?1) > park paths (1570 ng g^?1), indicating that significant positive correlation existed between PAH contamination and traffic density. PAHs in all samples were dominantly composed of 4-ring PAHs, accounting for 44.8% of the total. Pyrene, fluoranthene, and chrysene were the predominant individual components and accounted for 14.7% (1.2–19.2%), 12.9% (3.3–20.3%), and 11.0% (2.5–18.6%) of ΣPAHs, respectively. The specific isomer ratios indicated that traffic emission was the dominant source of PAHs in road dust. The incremental lifetime cancer risk values showed that cancer risk from exposure to road dust–borne PAHs was acceptable for local residents in Xinxiang.