Measured Polycyclic Aromatic Hydrocarbons Concentrations Research Articles

Organic matter imports to the Atacama Desert using polycyclic aromatic hydrocarbons as tracer

The Atacama Desert, despite its extreme hostile conditions, still harbours traces of life in its dusty surface. Until now, it remains open whether organic molecules found in topsoils have their origin from in-situ biotic processes in the hyper-arid core, or whether and to which degree they stem from outside the desert and its border regions. In order to trace atmospheric organic matter input, we analyzed the concentration of polycyclic aromatic hydrocarbons (PAHs) which almost exclusively derive from combustion processes and compared this to total organic carbon (TOC) concentrations. We sampled topsoil (0–15 cm depth) in one coastal (Paposo) and one inland aridity transect (Aroma) and compared them to atmospheric dust collected over two months in the hyper-arid core of the desert (Yungay). We found TOC and PAHs in all desert soil and dust samples. The sum of 18 analyzed PAHs ranged from 0.001 to 0.31 ng g−1 in the Paposo transect and from 0.14 to 0.78 ng g−1 in the Aroma transect, with moderate correlation (R2 = 0.68, p < 0.05) between TOC and PAHs. Measured PAH concentration in the dust was up to 5000 times higher and varied between 0.45 and 5.31 ng g−1. PAHs contributed with up to 0.25% to the TOC in dust and with 0.1% to the TOC in soils. This indicates that not all organic matter found in deserts is a trace for life defying extreme conditions, as it can also stem from sources outside or at the borders of the desert. We hence recommend verifying the origin of organic matter found in regions at the dry limit and highlight the overall presence of atmospheric pollutants on earth.

The Sources of Polycyclic Aromatic Hydrocarbons in Road Dust and Their Potential Hazard

Polycyclic aromatic hydrocarbons (PAHs) are persistent organic pollutants (POPs) found in the environment, posing significant health concerns for the population. This research aimed to assess the PAH levels in road dust near bus stops, identify their sources, and evaluate potential health risks. The analysis involved the use of a gas chromatography–flame ionization detector (GC-FID) to measure PAHs and absolute principal component score-multiple linear regression (APCS-MLR) for source apportionment of PAHs. The results indicated that the measured PAHs concentrations in road dust ranged from 137.8 to 5813 ng g−1, with Indeno[1,2,3-c,d]pyrene having the highest PAHs concentrations. The study identified three main sources of PAHs such as oil spills, fuel combustion, and coal burning, determined through APCS-MLR modeling. Further analysis revealed that the aggregate incremental lifetime cancer risk (ILCR) for children and adults were 2.16 × 10−6 and 2.08 × 10−6, respectively. Additionally, the hazard index (HI) for children exceeded that of adults, suggesting greater vulnerability to the potential health effects of PAH exposure. The findings indicate that long-term exposure to PAHs may negatively impact lung function and increase the risk of cancer and skin diseases. As a result, it is crucial for the local government to implement effective measures aimed at improving fuel quality and promoting green public transportation within the city. These initiatives may help mitigate PAH emissions and safeguard public health.

Integrative assessment of urban dust polycyclic aromatic hydrocarbons using ground and satellite data in Iran.

Recently, for quick urbanization and industrialization, pollutants, especially urban dust, have posed many threats to the human environment. Polycyclic aromatic hydrocarbons (PAHs) are regarded as the main dangerous pollutants that are widespread, persistent, and carcinogenic. The present work aimed to investigate the contamination and sources of PAHs, as well as to assess the risk of cancer for 16 priority PAHs, in urban dust samples in Ahvaz, Isfahan, and Shiraz cities in Iran. We measured PAH concentrations by gas chromatography-mass spectrometry (GC-MS). The average concentrations of the 16 PAHs in Ahvaz, Isfahan, and Shiraz were 6215.11, 7611.03, and 7810.37 μg kg-1, respectively. The domination of low-molecular-weight (LMW) PAHs was observed in Ahvaz, while maximum contribution was observed for high-molecular-weight (HMW) PAHs in Esfahan and Shiraz. For PAHs' source identification, diagnostic ratio, correlation analysis, clustering, and positive matrix factorization (PMF) model were used. PAHs had a combustion (coal and wood, oil, fossil fuels) and gasoline/diesel engine emissions in all cities. Comparative studies suggest that the PAH compounds' level is higher in the research area than in other countries, except for China and India. Also, the pollution of urban dust PAHs has increased over time compared to previous studies in the same cities. The cancer risk from exposure to dust contaminated with PAHs was assessed using the Incremental Lifetime Cancer Risk (ILCR) model. According to the findings, a high risk of exposure to cancer was observed in Ahvaz, Isfahan, and Shiraz. However, compared to adults, children are at higher risk of cancer in their daily lives via dermal contact and unconscious ingestion. Based on the ILCR values, the risk of cancer is in the order of Shiraz > Isfahan > Ahvaz. To assess air pollutants and their effects on urban dust, TROPOMI onboard the Sentinel-5P data were used in the studied cities during 2018-2021. The results show that Ahvaz has different high levels of CO compared to the other 2 cities. Also, Isfahan has different high levels of NO2 compared to the other 2 cities, but Shiraz has different low levels of O3. According to satellite time series data, the trend of the Aerosol Absorbing Index (AAI) has been increasing, while there was a decreasing trend in AAI from the beginning of the COVID-19 pandemic until 12 months later. Therefore, the natural and anthropogenic sources of urban dust PAHs have been increasing in all studied cities. Our findings show that PAH compounds in urban dust pose a significant threat to human health. Therefore, strategic management and planning are vital in reducing urban dust pollution.

Effect of polycyclic aromatic hydrocarbons on cancer risk causally mediated via vitamin D levels.

Polycyclic aromatic hydrocarbons (PAHs) widely exist in environmental substrates and are closely related to individual circulating vitamin D levels and tumorigenesis. Therefore, we proposed to evaluate the relationship between PAH exposure, vitamin D, and the risks for 14 cancer types via a causal inference framework underlying the mediation analysis. We evaluated seven urine monohydroxylated PAH (OH-PAH) and serum vitamin D concentrations of 3306 participants from the National Health and Nutrition Examination Survey between the 2013 and 2016 survey cycles and measured PAH concentrations in 150 subjects from the Nanjing cohort. We observed a significant negative dose-response relationship between increased OH-PAH levels and vitamin D deficiency. Each unit increase in ∑OH-PAHs could lead to a decrease in vitamin D levels (βadj = -0.98, Padj = 2.05 × 10-4 ). Body mass index could have interaction effects with ∑OH-PAHs and affect vitamin D levels. Coexposure to naphthalene and fluorene metabolites mutually affected vitamin D levels. Notably, vitamin D could causally mediate the relationship between OH-PAHs and nine types of cancer (e.g., colorectal cancer, liver cancers, etc.). This study first emphasizes the causal cascade of individual OH-PAHs, vitamin D, and cancer risk, providing insights into prevention via the environment.

PAH depletion in weathered oil slicks estimated from modeled age-at-sea during the Deepwater Horizon oil spill

During time-periods oil slicks are in the marine environment (age-at-sea), weathering causes significant changes in composition and mass loss (depletion) of oil spill chemicals including the more toxic polycyclic aromatic hydrocarbons (PAHs). The goal of this study was to estimate the age-at-sea of weathered oil slicks using the oil spill module of the Connectivity Modeling System and to use this age to interpret PAH concentration measurements. Percent depletion (PD) for each measurement was computed as the percentage difference between the original and measured PAH concentration in the crude oil and weathered oil slicks, normalized upon the mass losses relative to hopane. Mean PD increased with estimated age-at-sea for all PAHs. Less PD was observed for alkylated than for parent PAHs, likely due to decreasing vapor pressure with increasing degree of alkylation. We conclude that estimated age-at-sea can be used to explain PAH depletion in weathered oil slicks. We propose PAH vapor pressure can be coupled with the model to expand capacity for predicting concentration distributions of individual parent and alkylated PAHs in weathered oil along the coastline. This new module will advance the science supporting oil spill response by providing more certain estimates of health risks from oil spills.

An improved method to predict polycyclic aromatic hydrocarbons in surface freshwater by reducing the input parameters

Predicting the concentration of polycyclic aromatic hydrocarbons (PAHs) in surface freshwater are critical for understanding their spatio-temporal distribution, regulation effectiveness, and the subsequent health risks. In this study, by exploring the correlation of PAHs concentrations in surface freshwater (CPAHs) in China reported in the past twenty years with their emission (EPAHs), a novel relationship of CPAHs with EPAHs and PAHs properties (i.e., logKow and Sw) was established. For PAHs individual, percent sample deviation between the measured concentrations and the calculated concentrations are in the range of 18% to 48%, suggesting that the calculated concentrations of PAHs are well consistent with the measured PAHs concentration in surface freshwater. Moreover, spatial distribution of predicted PAHs concentrations in surface freshwater of China is also matched well with measured ones. Compared with other environmental models, the established relationships in this work can reduce the number of model parameters from dozens to three, as well as decrease percent sample deviation from several orders of magnitude to less than 50%. The established relationship of PAHs concentrations in surface freshwater with EPAHs, Sw, and logKow of PAHs, are valuable to facilitate the prediction of PAHs concentrations in surface freshwater by reducing monitoring costs.

Investigation of PAH and soot formation in a dimethyl ether (DME) laminar coflow diffusion flame

Dimethyl ether (DME) is an alternative fuel with significantly reduced particulate (i.e., soot) emissions. The polycyclic aromatic hydrocarbons (PAHs) and soot formation in pure DME flames have not been fully investigated and there is a need to develop a detailed understanding of soot formation from pure DME without the confounding effect of other more sooting hydrocarbons. Therefore, PAH and soot formation in a pure DME /air laminar coflow diffusion flame were explored in this study for two different initial temperatures of the fuel. Gas chromatography /mass spectroscopy (GC/MS), and time-resolved laser-induced incandescence (TiRe-LII) were used to quantitatively measure PAH concentrations, soot volume fractions and primary particle diameters. The experimental results show that, before the appearance of the soot particles, the gas phase reactions are dominated by PAHs smaller than three rings (A3: phenanthrene and anthracene), which decrease along the centerline as the soot volume fractions increase. The primary particle diameters remain relatively constant along the radial profiles at different flame heights, which suggests a moderate surface growth. The numerical predictions of soot and PAHs (smaller than A3) formation are consistent with the measurements (within a factor of 2.4), while the overprediction of the mole fraction of A3 is near an order of magnitude. The model can also capture the effect of increasing the initial fuel temperatures with reasonable accuracy. The experimental results suggest that PAHs are mainly formed by Hydrogen Abstraction Carbon (Acetylene) Addition (HACA), C1 addition is efficient for monoaromatic while the addition of C3 and species containing cyclopentadienyl moiety are not dominant for PAH growth. A database of the PAHs and soot formation has been created for further investigation of this DME flame.

Contamination and cancer risk assessment of polycyclic aromatic hydrocarbons (PAHs) in urban dust from different land-uses in the most populated city of Iran

Due to population growth and the considerable increase in usage of the resources, Human environment quality has been highly threatened by pollutants in recent decades. Polycyclic aromatic hydrocarbons (PAHs) are widespread, persistent organic pollutants which are of great concern due to their carcinogenicity. The present study is the first investigation that assesses contamination, sources and cancer risk of 16 priority PAHs proposed by US EPA in urban dust samples (n = 80) taken in different land-uses of Tehran metropolis, the capital of Iran. Gas chromatography-mass spectrometry (GC-MS) is used to measure PAHs concentrations. The results showed that the average concentration of the total 16 PAHs and the average Benzo[a]pyrene total potency equivalency were 566 μg kg−1 dry weight and 36.4 μg kg−1, respectively. In the commercial and residential land-uses high molecular weight (HMW) PAHs were dominated, whereas in green lands, light molecular weight (LMW) PAHs showed maximum contribution. The highest concentration of total PAHs were observed in the commercial areas due to limited air circulation and heavy traffic loads. Incremental Lifetime Cancer Risk (ILCR) model was applied to evaluate the cancer risk of exposure to PAHs contaminated dust. Based on the results, Tehran's residents (children and adults) in various land-uses except for green lands, are in high potential cancer risk of PAHs via ingestion and dermal contact exposure routs. Ace, Chr, Pyr, and BghiP which are indicators of traffic emissions, were found to be predominant PAH contributors in urban dust of commercial areas. Also, Ace, Fl, Phe, and BghiP which are derived from fossil fuel combustion, were mainly observed in the industrial land-use. Based on the results of factor analysis and diagnostic ratios, Diesel/gasoline engine vehicular emissions and combustion were found to be the main sources of PAHs in urban dust of Tehran.

In vitro and in silico AHR assays for assessing the risk of heavy oil-derived polycyclic aromatic hydrocarbons in fish

In the aftermath of the Great East Japan Earthquake of March 11, 2011, marine fish in Kesennuma Bay, Japan, have been contaminated with heavy oil containing polycyclic aromatic hydrocarbons (PAHs). To estimate the risk of six PAHs (benzo[α]pyrene, dibenzothiophene, phenanthrene, 2,3,5-trimethylnaphthalene, acenaphthene, and 1-methylphenanthrene), which have been detected at high levels in the tissues of fish from Kesennuma Bay, we attempted to evaluate the effects of these PAHs on the fish aryl hydrocarbon receptor (AHR) signaling pathway. We initially measured PAH concentrations and cytochrome P4501A catalytic activities (EROD: ethoxyresorufin-O-deethylase and MROD: methoxyresorufin-O-demethylase) as markers of AHR activation in greenlings (Hexagrammos otakii) collected from Kesennuma Bay in 2014. The results showed that alkylated PAH concentrations and EROD/MROD activities were higher in sites close to the oil-spilled sites than in the control site, suggesting AHR activation by spilled alkylated PAHs. We then investigated AHR-mediated responses to these PAHs in the in vitro reporter gene assay system where red seabream (Pagrus major) AHR1 (rsAHR1) or rsAHR2 expression plasmids were transiently transfected into COS-7 cells. The in vitro assay showed rsAHR isoform-, PAH-, and dose-dependent transactivation potencies. The relative effective concentrations of benzo[α]pyrene, dibenzothiophene, phenanthrene, 2,3,5-trimethylnaphthalene, acenaphthene, and 1-methylphenanthrene that induce 20% of the maximum benzo[α]pyrene response (REC20-BaP) for rsAHR1 activation were 0.052, 38, 79, 88, 270 nM, and no response, respectively, and those for rsAHR2 activation were 0.0049, 32, 53, 88, 60 nM, and no response, respectively. The results showed that the REC20-BaP values of benzo[α]pyrene for both the rsAHR1 and rsAHR2 isoforms were lower than the concentrations (0.041–0.20 nM) detected in the muscle tissue of fish from Kesennuma Bay, while the REC20-BaP values of other PAHs were higher than their tissue concentrations. In silico rsAHR homology modeling and subsequent ligand docking simulation analyses indicated that the rsAHR activation potencies of PAHs could be predicted from a rsAHR2 model. This study shows that in vitro and in silico rsAHR analyses may be a useful tool for assessing the risks to fish contaminated with PAHs.

Occurrence, source and ecological assessment of petroleum related hydrocarbons in intertidal marine sediments of the Bay of Fundy, New Brunswick, Canada

Total petroleum hydrocarbons (TPH), n-alkanes, petroleum-related biomarkers of terpanes and steranes, and polycyclic aromatic hydrocarbons (PAHs) were analyzed in the intertidal sediments in the Bay of Fundy, Nova Scotia/New Brunswick, Canada. Sites close to the harbour and more densely populated areas had higher TPH levels than other pristine areas. n-Alkanes presented a typical single bell-shape in n-C16 to n-C35 range and an obvious odd to even carbon preference. Most sites had trace amounts of petroleum biomarkers. Abundant non-alkylated PAHs and lower amounts of alkylated PAHs represented the major input of the incomplete combustion of solid (e.g., coal, coke, biomass, and coal tar) and liquid fuels. The toxicity estimation for PAHs indicates that they did not have potential toxicity to benthic organisms at most sampling sites. However, possible to probable negative effects from the measured PAH concentrations were found for the two samples from Courtenay Bay and Saint Andrews.

Availability of polycyclic aromatic hydrocarbons to earthworms in urban soils and its implications for risk assessment

Polycyclic aromatic hydrocarbons (PAHs) are a global problem, and in urban soils they can be found at potentially hazard levels. Nevertheless, the real risks that these contaminants pose to the environment are not well known, since the bioavailability of PAHs in urban soils has been poorly studied. Therefore, the bioavailability of PAHs in some selected urban soils from Lisbon (Portugal) was evaluated. Moreover, the applicability of a first screening phase based on total contents of PAHs was assessed. Results show that bioavailability of PAHs is reduced (low levels in earthworms, low accumulation percentages, and low biota-to-soil accumulation factors values), especially in more contaminated soils. The aging of these compounds explains this low availability, and confirms the generally accepted assumption that accumulation of PAHs in urban areas is mostly related with a long-term deposition of contaminated particles. The comparison of measured PAHs concentrations in earthworm tissues with the ones predicted based on theoretical models, reinforce that risks based on total levels are overestimated, but it can be a good initial approach for urban soils. This study also highlights the need of more reliable ecotoxicological data.

Occurrence of polycyclic aromatic hydrocarbons (PAHs) in mussel (Mytilus galloprovincialis) and eel (Anguilla anguilla) from Bizerte lagoon, Tunisia, and associated human health risk assessment

The aim of this study is to measure PAHs concentrations in mussels (Mytilus galloprovincialis) and fish (Anguilla anguilla) from the Bizerte lagoon (north Tunisia), and evaluate their distribution and sources, in order to provide a baseline of the state of PAH contamination in this lagoon and assess their human health risk. For this purpose, several native mussel and fish specimens were collected and analyzed using a high-performance liquid chromatography method with fluorescence detection for 15 EPA priority PAHs. PAHs levels in mussels and fish ranged from 107.4 to 430.7ngg−1 dw and 114.5–133.7ngg−1 dw, respectively. Naphthalene was the major component measured in mussels (31.5–272.6ngg−1 dw) and fish (57.9–68.6ngg−1 dw) and all specimens were classified as moderately contaminated. The PAHs composition pattern was similar for both species and was dominated by the presence of PAHs with 2- to 3-rings. The study of PAH ratios indicated a mixed petrogenic/pyrolytic origin. The health risks by consumption of these species was assessed and showed to present no threat to public health concerning PAH intakes. The results of this study would provide a useful aid for sustainable marine management in the region.

Monitoring of polycyclic aromatic hydrocarbons in a produced water disposal area in the Potiguar Basin, Brazilian equatorial margin.

The Potiguar Basin has oil and gas production fields offshore and onshore. All treated produced water (PW) from these fields is discharged through submarine outfalls. Although polycyclic aromatic hydrocarbons (PAHs) are minor constituents of PW, their input into the marine ecosystem is environmentally critical due to potential ecological hazards. A 2-year monitoring program was conducted in the vicinity of the outfalls to evaluate PAH bioaccumulation in marine life from PW discharges. The study was performed using transplanted bivalves Crassostrea brasiliana and semipermeable membrane devices (SPMDs) to measure PAH concentrations via bioaccumulation and in seawater. The bioaccumulation of PAH in transplanted bivalves reached up to 1105ngg(-1) in the vicinity of the monitored outfall. Significantly lower PAH concentrations were found in the reference area in comparison to the studied area around the outfalls. Time-integrated PAH concentrations in seawater ranged from 38 to 0.3ngL(-1) near the outfalls and from 10ngL(-1) to not detected in the reference area. Both measurement techniques were found to be effective for determining a gradient of descending PAH concentrations from the outfalls. In addition, this study also evaluated the bioavailability of PAH for local marine biota and provided information about the influence of PW discharges on the water quality of marine ecosystems.

Discontinuous and Continuous Indoor Air Quality Monitoring in Homes with Fireplaces or Wood Stoves as Heating System.

Around 50% of the world’s population, particularly in developing countries, uses biomass as one of the most common fuels. Biomass combustion releases a considerable amount of various incomplete combustion products, including particulate matter (PM) and polycyclic aromatic hydrocarbons (PAHs). The paper presents the results of Indoor Air Quality (IAQ) measurements in six houses equipped with wood burning stoves or fireplaces as heating systems. The houses were monitored for 48-h periods in order to collect PM10 samples and measure PAH concentrations. The average, the maximum and the lowest values of the 12-h PM10 concentration were 68.6 μg/m3, 350.7 μg/m3 and 16.8 μg/m3 respectively. The average benzo[a]pyrene 12-h concentration was 9.4 ng/m3, while the maximum and the minimum values were 24.0 ng/m3 and 1.5 ng/m3, respectively. Continuous monitoring of PM10, PAHs, Ultra Fine Particle (UFP) and Total Volatile Organic Compounds (TVOC) was performed in order to study the progress of pollution phenomena due to biomass burning, their trends and contributions to IAQ. The results show a great heterogeneity of impacts on IAQ in terms of magnitude and behavior of the considered pollutants’ concentrations. This variability is determined by not only different combustion technologies or biomass quality, but overall by different ignition mode, feeding and flame management, which can also be different for the same house. Moreover, room dimensions and ventilation were significant factors for pollution dispersion. The increase of PM10, UFP and PAH concentrations, during lighting, was always detected and relevant. Continuous monitoring allowed singling out contributions of other domestic sources of considered pollutants such as cooking and cigarettes. Cooking contribution produced an impact on IAQ in same cases higher than that of the biomass heating system.

The influence of sunlight and oxidative treatment on measured PAH concentrations in biochar

The concentration changes of 18 different polycyclic aromatic hydrocarbons (PAHs) in two different biochars were assessed after (1) chemical oxidative treatment with a solution ofH2O2 andNa2S2O8, (2) exposure to sunlight with intermittent wetting, and (3) exposure to sunlight with intermittent wetting after mixing inZnO and Na2S2O8. Chemical oxidative treatment of biochars derived from gasified wood biochar and a gasified wood/Arundo donax mixture led to decreases in six-ring PAHs, but overall significant increases in measured PAH concentration sums for both biochars (from 225 ± 7 to 312 ± 18μgg(-1) for wood-derived and 165 ± 3 to 244 ± 7μgg(-1) for mixture-derived). Sunlight exposure of the mixture-derived biochar led to increases in some three- and four-ring PAHs, but overall decreases in summed PAH concentrations (165 ± 3 to 60 ± 1μgg(-1) with wetting only and 165 ± 3 to 41 ± 4μgg(-1) when Na2S2O8 and ZnO were included). The mass losses in the sunlight-exposed samples primarily were due to losses of low molar mass (two-ring) PAHs, though high molar mass (five- and six-ring) PAH concentrations also decreased. This result implies sun and rain exposure to biochar, prior to agricultural application, will help reduce potential PAH soil contamination from the biochar.

Evaluation of PAH contamination in soil treated with solid by-products from shale pyrolysis.

The aim of this work was to evaluate the concentrations of polycyclic aromatic hydrocarbons (PAHs) in soils to which solid shale materials (SSMs) were added as soil conditioners. The SSMs were derived from the Petrosix pyrolysis process developed by Petrobras (Brazil). An improved ultrasonic agitation method was used to extract the PAHs from the solid samples (soils amended with SSMs), and the concentrations of the compounds were determined by gas chromatography coupled to mass spectrometry (GC-MS). The procedure provided satisfactory recoveries, detection limits, and quantification limits. The two-, three-, and four-ring PAHs were most prevalent, and the highest concentration was obtained for phenanthrene (978 ± 19 μg kg(-1) in a pyrolyzed shale sample). The use of phenanthrene/anthracene and fluoranthene/pyrene ratios revealed that the PAHs were derived from petrogenic rather than pyrogenic sources. The measured PAH concentrations did not exceed national or international limit values, suggesting that the use of SSMs as soil conditioners should not cause environmental damage.

Potential source apportionment of polycyclic aromatic hydrocarbons in surface sediments from the middle and lower reaches of the Yellow River, China.

In this work, principal component analysis/multiple linear regression (PCA/MLR), positive matrix factorization (PMF), and UNMIX model were employed to apportion potential sources of polycyclic aromatic hydrocarbons (PAHs) in surface sediments from middle and lower reaches of the Yellow River, based on the measured PAHs concentrations in sediments collected from 22 sites in November 2005. The results suggested that pyrogenic sources were major sources of PAHs. Further analysis indicated that source contributions of PAHs compared well among PCA/MLR, PMF, and UNMIX. Vehicles contributed 25.1-36.7 %, coal 34.0-41.6 %, and biomass burning and coke oven 29.2-33.2 % of the total PAHs, respectively. Coal combustion and traffic-related pollution contributed approximately 70 % of anthropogenic PAHs to sediments, which demonstrated that energy consumption was a predominant factor of PAH pollution in middle and lower reaches of the Yellow River. In addition, the distributions of contribution for each identified source category were studied, which showed similar distributed patterns for each source category among the sampling sites.

Source Apportionment of PAHs Using Unmix Model for Yantai Costal Surface Sediments, China

16 Polycyclic aromatic hydrocarbons (PAHs) in 20 surface sediments from Yantai offshore area were measured. The total PAHs concentrations varied from 450.0 to 4,299.0 ng/g, with a mean of 2,492.9 ng/g. The high molecular weight (HMW) PAHs were most abundant and the ratio ranged from 54.9 % to 81.6 % in all sampling stations, indicating that pyrogenic sources were a predominant contribution to PAHs pollution. The source contributions of PAHs were estimated based on the EPA Unmix 6.0 receptor model. The data were well simulated due to a high correlation coefficient between predicted and measured PAHs concentration (R(2) = 0.99). A mixed source of coal combustion and traffic pollution contributed to 38.9 % of the measured PAHs, followed by diesel emission (38.8 %) and a mixed source of biomass combustion and gasoline engine emissions (22.3 %). The current findings further validated that Unmix model could be applied to apportion the sources of PAHs in sediments.

Source Apportionment of Polycyclic Aromatic Hydrocarbons in Agricultural Soils of Yanqing County in Beijing, China

Guanting Reservoir in Yanqing County is a strategic drinking-water resource for Beijing, China. The agricultural soil samples (0 cm to 20 cm) were collected to determine the concentration, compositional profiles, and sources of polycyclic aromatic hydrocarbons (PAHs) surrounding the reservoir. The average measured PAH concentration was 140 ± 85.7 μg kg−1 (CV = 0.45) (dry weight or dw; n = 48; shown as arithmetic mean and standard deviation), which is lower than most of the results reported in literature. The PAH compositional profiles were dominated by 3- and 4-ring compounds, particularly phenanthrene (PHE), fluoranthene (FLA), fluorene (FLO), and pyrene (PYR). The PAH sources were estimated by analyzing the corrected ratios of isomeric PAH species derived using the multimedia fugacity model and principal component analysis/multiple linear regression (PCA/MLR). The corrected isomeric ratios of FLA/(FLA+PYR) and anthracene (ANT)/(ANT+PHE) indicate that combustion processes are the major sources of PAHs in the soil. Three principal components were identified as main sources, representing coal burning and traffic exhaust, biomass combustion and coking, and a source labeled “other,” which contribute 54%, 40%, and 6% of the total PAH, respectively (α = 0.05). Moreover, except those from local biomass burning, other PAHs were primarily deposited in the soil from distant sources via atmospheric transportation.

Probabilistic ecological risk assessment of polycyclic aromatic hydrocarbons in southwestern catchments of the Bohai Sea, China

A probability risk assessment was undertaken to study the individual and combined ecological risks induced by six polycyclic aromatic hydrocarbons (PAHs) both in surface water and sediment from southwestern catchments of the Bohai Sea, China. The actual measured PAH concentrations in water and sediment were compared with toxicity effect data (the 10th percentile of predicted no effect concentration) to calculate the risk quotients (RQs) for an individual PAH. The equilibrium partitioning method was applied to estimate toxicity data in sediment. A method based on the equivalent concentration concept was proposed and applied to assess the combined ecological risk of multiple PAHs. Monte Carlo simulation and bootstrap technique were utilized to calculate the distribution of RQs and associated uncertainties. The ecological safety level was defined by RQ ≤ 1. Results indicated that both in water and sediment, fluoranthene and pyrene posed the highest risks, whereas acenaphthene and fluorene posed negligible risks. Naphthalene and phenanthrene did not pose risks to the ecological community in surface water but had relatively higher risks in sediment. The median RQs of combined risk in surface water and sediment were 0.934 and 2.42, and the probabilities of RQ > 1 were up to 0.473 and 0.599, respectively, which were much higher than the individual compound acting alone. The risk level in sediment was quite higher than in surface water probably owing to the non-equilibrium distribution between two phases, which suggested that local authorities should focus more on sediment quality management.