Levels Of Polycyclic Aromatic Hydrocarbons Research Articles

Chemical contamination affecting filter-feeding bivalves in no-take marine protected areas from Brazil

Marine protected areas (MPAs) are zones geographically delimited under pre-defined management goals, seeking to reduce anthropogenic threats to biodiversity. Despite this, in recent years reports of MPAs affected by chemical contamination has grown. Therefore, this study addresses this critical issue assessing legacy and current chemical contamination in filter-feeder bivalves obtained in very restrictive no-take MPAs from Brazil. The detected pollutants encompass polycyclic aromatic hydrocarbons (PAHs), linear alkylbenzenes (LABs), and persistent organic pollutants (POPs) like dichlorodiphenyltrichloroethane (DDTs) and polychlorinated biphenyls (PCBs). Despite protective measures, bivalves from nine MPAs exhibited high LABs (13.2–1139.0 ng g−1) and DDTs levels (0.1–62.3 ng g−1). PAHs were present in low concentrations (3.1–29.03 ng g−1), as PCBs (0.7–6.4 ng g−1), hexachlorobenzene (0.1–0.2 ng g−1), and Mirex (0.1–0.3 ng g−1). Regardless of the sentinel species, MPAs and management categories, similar accumulation patterns were observed for LABs, DDTs, PAHs, and PCBs. Based on the limits proposed by Oslo Paris Commission, the measured levels of PAHs, PCBs and were below the environmental assessment criteria. Such findings indicate the no biological effects are expected to occur. However, they are higher considering background conditions typically measured in remote or pristine areas and potential simultaneous exposure. Such findings indicate an influence of anthropogenic sources, emphasizing the urgency for monitoring programs guiding strategic management efforts to safeguard these areas.

Water Quality and the First-Flush Effect in Roof-Based Rainwater Harvesting, Part I: Water Quality and Soil Accumulation

Rainfall runoff may be captured and stored for later use, but the quality of this water can be detrimental in some uses without the use of appropriately designed first-flush diverters. The rainfall runoff water quality was measured on nineteen new small-scale and two aged commercial roofs located near high traffic highways. Roof coverings included asphalt shingles, sheet metal, clay tiles, and tar and gravel. Runoff samples were evaluated for polycyclic aromatic hydrocarbons (PAHs), phosphorus flame retardants (PFRs), and pyrethroid insecticides. Eighteen small-scale roofs were subjected to a range of simulated rainfall events, while natural runoff was sampled on the commercial roofs and one small-scale roof. Runoff was analyzed for pH, conductivity, turbidity, total suspended solids, boron, iron, copper, zinc, manganese, sodium adsorption ratio, nitrate-nitrogen, seventeen PAHs, tris(2-chloroethyl) phosphate, tris(1,3-dichloro-2-propyl)phosphate, bifenthrin, cypermethrin, and lambda-cyhalothrin. Samples from four natural storm events were also analyzed for total coliforms and Escherichia coli. In addition, soils below seventeen existing gutter downspouts were sampled to determine long-term pollutant accumulation. Atmospheric deposition was the main contributor of pollutants in the roof runoff. A majority of samples fell within the U.S. EPA guidelines for non-potable urban and agricultural water reuse. Trace levels of PAHs, PFRs, and insecticides were detected, but all detections were three orders of magnitude below the USGS health-based screening level benchmark concentrations. Results indicate that diverting the first flush, based on turbidity, total suspended solids, or conductivity, can improve the overall water quality and reduce the concentrations of PAHs in harvested rainwater. Downspout soil sampling showed potential for the long-term accumulation of PAHs at concentrations exceeding the minimum human-health risk-based screening levels at these high runoff-loading locations.

Effects of Chinese “double carbon strategy” on soil polycyclic aromatic hydrocarbons pollution

Polycyclic aromatic hydrocarbons (PAHs) and carbon dioxide primarily originate from the combustion of fossil fuels and biomass. The implementation of the Chinese “double carbon strategy” is expected to impact the distribution of PAH emissions, consequently influencing the spatial distribution trend of PAHs in surface soil. Therefore, it is crucial to quantitatively evaluate the effectiveness of the Chinese “double carbon strategy” on soil PAH pollution for the purpose of “the reduction of pollution and carbon emissions”. This study utilized 15,088 individual PAH concentration data from 943 soil samples collected between 2003 and 2020 in China, in conjunction with PAH emissions at a 10 km resolution, for meta-analysis. The calculated PAH emissions in this study are in line with the global PAH emission inventory (PKU-PAH-2007), with a relative standard deviation at the provincial level of less than 25 %. Subsequently, a novel method was developed using emission density and Kow of PAHs to predict PAH concentrations in surface soil based on a least-squares regression model. Compared to other environmental models, the method established in this study significantly reduced the percent sample deviation to less than 70 %. Furthermore, energy consumption data for China were simulated based on the implementation plan of the “double carbon strategy” to project PAH emissions and soil PAH levels for the years 2030 and 2060. The predicted PAH emissions in China were estimated to decrease to 41,300 t in 2030 and 10,406.5 t in 2060 from 78,815 t in 2020. Moreover, the heavily contaminated areas of soil PAHs (i.e., total PAH concentrations in soil exceeding 1000 μg kg−1) were projected to decrease by 45 % and 82 % in 2030 and 2060, respectively, compared to levels in 2020. These findings suggest that the implementation of the “double carbon strategy” can fundamentally reduce the pollution of PAHs in surface soil of China.

Dust dynamics: distribution patterns of semi-volatile organic chemicals across particle sizes in varied indoor microenvironments.

An extensive analysis of the distribution patterns of three distinct classes of semi-volatile organic chemicals (SVOCs)-phthalates (PAEs), organophosphate flame retardants (OPFRs), and polycyclic aromatic hydrocarbons (PAHs)-across four distinct size fractions of dust (25, 50, 100, and 200μm) was conducted. The dust samples were sourced from AC filter, covered car parking lots, households, hotels, mosques, and car floors. To generate the four fractions, ten dust samples from each microenvironment were pooled and sieved utilizing sieving apparatus with the appropriate mesh size. Selected SVOCs were quantified utilizing gas chromatography-mass spectrometry in electron impact (EI) mode. Results unveiled diverse contamination levels among dust fractions, showcasing car parking lot dust with the lowest chemical contamination, while car floor dust displayed the highest levels of PAHs and OPFRs, peaking at 28.3µg/g and 43.2µg/g, respectively. In contrast, mosque and household floor dust exhibited the highest concentrations of phthalates, with values of 985µg/g and 846µg/g, respectively. Across the analyzed microenvironments, we observed a trend where concentrations of SVOCs tended to rise as dust particles decreased in size, forming a visually striking pattern. This phenomenon was particularly pronounced in dust samples collected from car floors and parking lots. Among SVOCs, PAEs emerged as the predominant contributors with > 90% followed by OPFRs and PAHs. The high levels of OPFRs in car floor dust align logically with the fact that numerous interior components of cars are treated with OPFRs, within a compact indoor microenvironment, to comply to fire safety regulations. Furthermore, petroleum products are a major source of PAHs in the environment and all the sampled cars in the study had combustion engines. Consequently, car dust is more likely to be polluted with PAHs stemming from petroleum combustion. Although previous investigations have noted an increase in heavy metals and brominated flame retardants with decreasing dust particles, this is the first study analyzing these SVOCs in different fractions of dust from various microenvironments. However, aside from two specific microenvironments, the observed pattern of escalating SVOC concentrations with smaller dust particle sizes was not corroborated among the examined microenvironments. This divergence in concentration trends suggests the potential involvement of supplementary variables in influencing SVOC distributions within dust particles.

Residual polycyclic aromatic hydrocarbons and firefighters' hematological profile

IntroductionFirefighters are exposed to polycyclic aromatic hydrocarbons (PAHs) during fire suppression, but the extent of PAH penetration through turnout gear and its impact on blood cell components remains uncertain. The main objective of this study is to investigate the residual levels of PAHs on turnout gear and skin, and to assess their potential effects on blood cell components in firefighters. We hypothesize that firefighting activities lead to increased PAH exposure, which in turn may induce alterations in blood cell composition. We also hypothesize that differences in PAH exposure and corresponding blood cell changes will be observed between volunteer and career firefighters.MethodsForty-seven firefighters were recruited from 11 fire departments in Oklahoma. PAH levels on gear and skin were measured, and complete blood count (CBC) parameters were analyzed. Parametric and non-parametric tests were used to examine differences in PAH exposures and hematological profiles between volunteer and career firefighters and possible changes over time. Generalized estimating equation (GEE) models were performed to assess the relationships between PAHs and blood cells.ResultsOur analysis revealed significant hematological differences between volunteer and career firefighters, with volunteers exhibiting lower aerobic capacity and higher systemic inflammation. Increased levels of specific PAHs were found on volunteers' gear post-fire.ConclusionOur findings indicate an association between PAH exposure and changes in blood parameters, emphasizing the need for improved decontamination protocols and protective measures, particularly for volunteer firefighters.

Presence of polycyclic aromatic hydrocarbons and persistent organochlorine pollutants in human Milk: Evaluating their levels, association with Total antioxidant capacity, and risk assessment

Breastfeeding provides numerous health benefits for both infants and mothers, promoting optimal growth and development while offering protection against various illnesses and diseases. This study investigated the levels of polychlorinated biphenyls (PCB), organochlorine pesticides (OCP) and polycyclic aromatic hydrocarbons (PAH) in human milk sampled in Zadar (Croatia). The primary objectives were twofold: firstly, to evaluate the individual impact of each compound on the total antioxidant capacity (TAC) value, and secondly, to assess associated health risks. Notably, this study presents pioneering and preliminary insights into PAH levels in Croatian human milk, contributing to the limited research on PAH in breast milk worldwide. PCB and OCP levels in Croatian human milk were found to be relatively lower compared to worldwide data. Conversely, PAH levels were comparatively higher, albeit with lower detection frequencies. A negative correlation was established between organic contaminant levels and antioxidative capacity, suggesting a potential link between higher antioxidative potential and lower organic contaminant levels. Diagnostic ratio pointed towards traffic emissions as the primary source of the detected PAH. The presence of PAH suggests potential health risk, underscoring the need for further in-depth investigation.

Occurrence and characteristics of PAHs in coastal seawater off the city of Samsun on the Black Sea coast of Turkey

Polycyclic aromatic hydrocarbons (PAHs) concentrations in seawater were monitored seasonally along the Samsun coast, Turkey, between August 2019 and May 2020 to elucidate main origin, seasonal variations, and risk pathways of PAHs. Total PAH concentrations in surface seawater ranged from 24.86 to 477.78 ng L−1 (mean 138.90, SD 62.22 ng L−1), with relatively higher levels in summer and autumn seasons. Combustion products were the major sources of PAHs. The increased PAH levels during the summer period may have resulted from the more intense industrial and agricultural activities. The highest proportion of PAHs were 3- and 2-ringed, accounting for 39.23 % and 26.50 % of ΣPAHs, respectively, and their derivatives Nap and Phe predominated in individual PAHs. While RQ values of ∑PAHs showed low ecological risk, RQMPCs of BpF and BaA in autumn and BpF in summer were at high ecological risk.

Effect of changes in the fuel type of thermal power plants on the spatial distribution and levels of PAH pollution in the Vorkuta agglomeration beyond the Arctic Circle

The paper is a study of the composition of 15 polycyclic aromatic hydrocarbons (PAHs) in the snow cover of Vorkuta (Komi Republic) in the impact zone of the fuel and energy complex in 2017 and 2023. We have identified high aerotechnogenic pollution of the Vorkuta city and adjacent territories with PAHs during heating with fuel oil and coal, with a mean concentration of 301.6 ng/L (meltwater plus particles) and spatial distribution of 85.2 μg/m2. There is a significant decrease in PAH levels when the fuel for thermal power plants has been changed to natural gas, with a mean concentration of 26.1 ng/L (meltwater plus particulates) and spatial distribution of 4.9 μg/m2. The deposition areas of different PAH fractions are identified in the impact zones of Thermal Power Plants 1 and 2, the Central Boiler House and the urbanised areas of the Vorkuta agglomeration. 2-4-ring PAHs dominate in the emissions, accounting for 92–100 % of the sum of PAHs from coal/oil combustion and 66–93 % from natural gas combustion. The indicator ratios of PAHs in the snow cover of Vorkuta in both 2017 and 2023 indicate their predominantly pyrogenic genesis. The environmental risk coefficients of PAHs in the snow cover and their change from 2017 to 2023 are calculated. TEQ changed from 2.1 ng/L (mean) in the 2017 season to 1.7 ng/L (mean) in the 2023 season. The risk quotients have been reduced from moderate risk to low risk. Reconstruction of thermal power plants when replaced by more environmentally friendly fuel (natural gas) reduces the amount of atmospheric emissions of organic pollutants.

Occurrence, removal, and risk assessment of polycyclic aromatic hydrocarbons and their derivatives in typical wastewater treatment plants

Wastewater treatment plants (WWTPs) have a certain removal capacity for polycyclic aromatic hydrocarbons (PAHs) and their derivatives, but some of them are discharged with effluent into the environment, which can affect the environment. Therefore, to understand the presence, sources, and potential risks of PAHs and their derivatives in WWTPs. Sixteen PAHs, three chlorinated polycyclic aromatic hydrocarbons (ClPAHs), three oxidized polycyclic aromatic hydrocarbons (OPAHs), and three methylated polycyclic aromatic hydrocarbons (MPAHs) were detected in the influent and effluent water of three WWTPs in China. The average concentrations of their influent ∑PAHs, ∑ClPAHs, ∑OPAHs, and ∑MPAHs ranged from 2682.50 to 2774.53 ng/L, 553.26–906.28 ng/L, 415.40–731.56 ng/L, and 534.04–969.83 ng/L, respectively, and the effluent concentrations ranged from 823.28 to 993.37 ng/L, 269.43–489.94 ng/L, 285.93–463.55 ng/L, and 376.25–512.34 ng/L, respectively. The growth of heat transport and industrial energy consumption in the region has a significant impact on the level of PAHs in WWTPs. According to the calculated removal efficiencies of PAHs and their derivatives in the three WWTPs (A, B, and C), the removal rates of PAHs and their derivatives were 69–72%, 62–71%, and 68–73%, respectively, and for the substituted polycyclic aromatic hydrocarbons (SPAHs), the removal rates were 41–49%, 31–40%, and 33–39%, respectively; moreover, the removal rates of PAHs were greater than those of SPAHs in the WWTPs. The results obtained via the ratio method indicated that the main sources of PAHs in the influent of WWTPs were the combustion of coal and biomass, and petroleum contamination was the secondary source. In risk evaluation, there were 5 compounds for which the risk quotient was considered high ecological risk. During chronic disease evaluation, there were 11 compounds with a risk quotient considered to indicate high risk. PAHs and SPAHs with high relative molecular masses in the effluent of WWTPs pose more serious environmental hazards than their PAHs counterparts.

Biomonitoring polycyclic aromatic hydrocarbon levels in domestic kitchens using commonly grown culinary herbs

Cooking is a significant source of polycyclic aromatic hydrocarbon (PAHs) emissions in indoor environments. A one-month biomonitoring study was carried out in previously selected rural Hungarian kitchens to evaluate cooking-related PAHs concentrations in 4 common kitchen vegetables such as basil, parsley, rocket and chives. The study had two mainobjectives: firstly, to follow PAHs accumulation pattern and to find out if this pattern can be associated with different cooking habits. Also, the usefulness of culinary herbs for indoor bioaccumulation studies was assessed. The 2-ring naphthalene was the dominant PAH in the majority of the samples, its concentrations were in the range of 25.4 µg/kg and 274 µg/kg, of 3-ring PAHs the prevalency of phenanthrene was observed, with highest concentration of 62 µg/kg. PAHs accumulation pattern in tested plants clearly indicated differences in cooking methods and cooking oils used in the selected households. Use of lard and animal fats in general resulted in the high concentrations of higher molecular weight (5- and 6-ring) PAHs, while olive oil usage could be associated with the emission of 2- and 3-ring PAHs. Culinary herbs, however, accumulated carcinogenic PAHs such as benzo[a]anthracene (highest concentration 11.9 µg/kg), benzo[b]fluoranthene (highest concentration 13.8 µg/kg) and chrysene (highest concentration 20.1 µg/kg) which might question their safe use.

Identification and health risk evaluation of soil contaminated by polycyclic aromatic hydrocarbons at shale gas extraction sites based on positive matrix factorization

The impact of shale gas extraction on surrounding environmental media remains unclear. In this study, the current state of contamination by polycyclic aromatic hydrocarbons (PAHs), which are high-frequency contaminants of shale gas, was investigated in the soil surrounding emerging shale gas development sites. The source analysis of PAHs was conducted in the soils of shale gas extraction sites using positive matrix factorization (PMF). The health risk assessment (HRA) was calculated for ingestion, dermal contact, and inhalation exposures, and the priority sources of PAHs in the soil were jointly identified by PMF and HRA to refine the contribution level of different individual PAHs to the carcinogenic risk. The results showed that both Sichuan and Chongqing mining site soils were contaminated to different degrees. Shale gas extraction has an impact on the surrounding soil, and the highest contributing source of PAHs in the mining site soil of Sichuan was anthropogenic activity, accounting for 31.6%, whereas that in the mining site soil of Chongqing was biomass combustion and mixed automobile combustion, accounting for 35.9%. At the two mining sites in Sichuan and Chongqing, none of the three exposure pathways (ingestion, dermal contact, and inhalation) posed a carcinogenic risk to children, whereas the dermal exposure pathway posed a carcinogenic risk to adults. Health risk assessments based on specific source assignments indicate that when managing soil pollution, the control of fossil fuel combustion and vehicular emissions should be prioritized.

Temporal and spatial distribution of polycyclic aromatic hydrocarbons (PAHs) in the Danube River in Hungary

The Danube is a significant transboundary river on a global scale, with several tributaries. The effluents from industrial operations and wastewater treatment plants have an impact on the river's aquatic ecosystem. These discharges provide a significant threat to aquatic life by deteriorating the quality of water and sediment. Hence, a total of 16 Polycyclic Aromatic Hydrocarbons (PAHs) compounds were analyzed at six locations along the river, covering a period of 12 months. The objective was to explore the temporal and spatial fluctuations of these chemicals in both water and sediment. The study revealed a significant fluctuation in the concentration of PAHs in water throughout the year, with levels ranging from 224.8 ng/L during the summer to 365.8 ng/L during the winter. Similarly, the concentration of PAHs in sediment samples varied from 316.7 ng/g in dry weight during the summer to 422.9 ng/g in dry weight during the winter. According to the Europe Drinking Water Directive, the levels of PAHs exceeded the permitted limit of 100 ng/L, resulting in a 124.8% rise in summer and a 265.8% increase in winter. The results suggest that the potential human-caused sources of PAHs were mostly derived from pyrolytic and pyrogenic processes, with pyrogenic sources being more dominant. Assessment of sediment quality standards (SQGs) showed that the levels of PAHs in sediments were below the Effect Range Low (ERL), except for acenaphthylene (Acy) and fluorene (Fl) concentrations. This suggests that there could be occasional biological consequences. The cumulative Individual Lifetime Cancer Risk (ILCR) exceeds 1/104 for both adults and children in all sites.

Effects of polystyrene nano- and microplastics and of microplastics with sorbed polycyclic aromatic hydrocarbons in adult zebrafish

The presence of nanoplastics (NPs) and microplastics (MPs) in the environment is recognised as a global-scale problem. Due to their hydrophobic nature and large specific surface, NPs and MPs can adsorb other contaminants, as polycyclic aromatic hydrocarbons (PAHs), and modulate their bioavailability and hazard. Adult zebrafish were exposed for 3 and 21 days to: (1) 0.07 mg/L NPs (50 nm), (2) 0.05 mg/L MPs (4.5 μm), (3) MPs with sorbed oil compounds of the water accommodated fraction (WAF) of a naphthenic crude oil (MPs-WAF), (4) MPs with sorbed benzo(a)pyrene (MPs-B(a)P), (5) 5 % WAF and (6) 21 μg/L B(a)P. Electrodense particles resembling NPs were seen in the intestine lumen close to microvilli. MPs were abundantly found in the intestine lumen, but not internalised into the tissues. After 21 days, NPs caused a significant downregulation of cat, and upregulation of gpx1a and sod1, while MPs upregulated cyp1a and increased the prevalence of liver vacuolisation. No histopathological alteration was observed in gills. In this study, contaminated MPs did not increase PAH levels in zebrafish but results highlight the potential differential impact of plastic particles depending on their size, making it necessary to urgently address the ecotoxicological impact of real environmental NPs and MPs.

Biostimulation potentials of spent milled maize and cowblood on a crude oil polluted soil

This study was carried out to investigate the biostimulation effect of the application of spent milled maize and cow blood to crude oil polluted soil. The treatment groups were; Control (0 L crude oil (CO) + 0 kg spent milled maize (SMM)), group 1 (1 L CO + 1 kg SMM + 1 L cow blood), group 2 (2 L CO + 2 kg SMM) and group 3 (5 L CO + 5 kg SMM). The experiment was laid out in a completely randomized design A total of four treatment combinations were applied and replicated 3 times giving a total of 48 plots.The physicochemical properties and bacterial load of the soil were determined before pollution, two weeks after pollution, four weeks and eight weeks after remediation. The results for physicochemical properties of soil indicates a decrease in total organic carbon and nitrogen while there was an increase in the levels of cation exchange capacity, phosphorus and electrical conductivity after crude oil pollution. The mean levels of total petroleum hydrocarbon and polycyclic aromatic hydrocarbon reduced after the pollution. The application of the spent milled maize and cow bloodwere observed to improve the physicochemical properties of soil. There was also an increased bacterial count for the treated groups compared to the control; the values ranged from 1.3 x 103cfu/g to 1.24 x 108cfu/g. The identified bacteria were Flavobacterium, Pseudomonas, Bacillus, Micrococcus, Proteus, Clostridium and Nocardia species.Generally, this study has revealed that spent milled maize and cow blood are effective in the restoration of crude oil polluted soil.

Can environmental factors increase oxidative responses in fish exposed to polycyclic aromatic hydrocarbons (PAHs)?

Relations among polycyclic aromatic hydrocarbons (PAHs), biomarkers of oxidative stress (lipid peroxidation, glutathione, and glutathione S-transferase activity), and the possible influence of environmental factors (temperature, pH, and salinity) were assessed in situ for specimens of Ramnogaster arcuata, a native estuarine fish. PAH levels found in the muscular tissue of R. arcuata ranged from 0.7 to 293.4 ng g−1 wet weight with petrogenic and pyrolytic inputs. Lipid peroxidation in the liver showed positive correlations (P < 0.05) with total PAHs (r = 0.66), 3-ring (r = 0.66) and 4-ring PAHs (r = 0.52) and glutathione in muscle (r = 0.58). Significant positive correlations (P < 0.05) were also evidenced between muscular glutathione with total (r = 0.62) and 3-ring PAHs (r = 0.75). Hepatic glutathione S-transferase negatively correlated with 4-ring PAHs (r = −0.58). These correlations suggest that lipid peroxidation and muscular glutathione could be good biomarkers for complex mixtures of PAHs, and hepatic glutathione S-transferase could be a suitable biomarker for 4-ring PAHs. Furthermore, significant correlations (P < 0.05) of environmental factors with PAH levels and biomarkers were observed, especially pH with 3-ring PAHs (r = −0.65), lipid peroxidation (r = −0.6), glutathione in the liver (r = −0.73) and muscle (r = −0.75); and temperature with 2-ring PAHs (r = −0.75) and glutathione in muscle (r = 0.51). The data suggest an influence of physicochemical parameters which could be driving a shift in PAH toxicity in R. arcuata. These results are essential for an integrated understanding of ecotoxicology and could help to predict environmental effects in present and future scenarios of ocean warming and acidification.

Melanin-mediated accumulation of polycyclic aromatic hydrocarbons in human hair: Insights from biomonitoring and cell exposure studies

While human hair is widely used to monitor micro-organic contaminants (MOCs), their incorporation mechanisms are poorly understood. Melanin, known to facilitate the accumulation of drugs in hair, hasn’t been studied in the field of MOCs. Here, polycyclic aromatic hydrocarbons (PAHs), a class of priority MOCs, were investigated through hair biomonitoring as well as cell exposure experiments. PAH concentrations and melanin contents were measured in black and white hairs from the same individual. The results showed that five dominant PAHs (phenanthrene, fluoranthene, pyrene, benzo[a]anthracene and chrysene) in black hair (0.66 ng/g – 35.1 ng/g) were significantly higher than those in white hair (0.52 ng/g – 29.6 ng/g). Melanin contents in black hair (14.9 – 48.9 ng/g) were markedly higher than in white hair (0.35 – 2.15 ng/g) and were correlated to PAH concentrations, hinting melanin-mediated accumulation of PAHs in hair. The in vitro experiment using murine melanoma cells demonstrates that PAH levels in cells were affected by melanin, suggesting the affinity of melanin to PAHs. Both biomonitoring and cell exposure experiment implicate the pivotal role of melanin in PAH accumulation in hair. Therefore, to ensure the accuracy of hair biomonitoring for MOCs, attention must be paid to the melanin content uniformity.

Characterization of polycyclic aromatic hydrocarbons in mangrove sediments from Ifiekporo Creek, Warri, Nigeria

The occurrence and level of polycyclic aromatic hydrocarbons (PAHs) in mangrove sediment from Ifiekporo Creek in Warri, Delta State, Nigeria, were assessed in this study. The extraction of PAHs from the sediment samples was achieved using the PAH analytical test method (USEPA 8270). This method measures the individual concentrations of extractable PAHs in samples. The PAHs were quantified within the C11-C22 subgroup. The basic GC parameters for the analysis of polyaromatic hydrocarbons were analysed using a gas chromatography‒mass selective detector (GC‒MSD). The individual PAH concentrations in the mangrove sediment samples ranged from 850 µg/kg−1 to 3470 µg/kg−1. PAH source apportionment employing isomeric ratios and multivariate statistics indicated both pyrogenic and petrogenic source inputs in the sediment samples. The order of PAH homology in the sediment was 3-ring > 2-ring > 4-ring. The sediment samples were mostly dominated by LMW PAHs. The results of the ecological risk assessment in the study area indicate that there is low ecological risk associated with PAH exposure in sediment. These results provide data on the concentrations and compositional patterns of PAHs, which is useful for understanding the effects, sources, fates, and transport of PAHs in sediment in the study area, as well as for providing relevant information for environmental quality management and forensic studies.

Personal exposure monitoring to polycyclic aromatic hydrocarbons bound to size-segregated aerosol

Air pollution is a global problem, where impaired air quality significantly damages human health and the environment. Twenty-four hours of personal exposure to size-segregated airborne particulate matter (PM) and associated polycyclic aromatic hydrocarbons (PAHs) were measured in 129 non-smoking residents living in two Czech cities, Ostrava (an industrial area with high levels of air pollution) and Ceske Budejovice (an agricultural area with lower air pollution level) in various seasons between years 2018–2020. Particulate matter (PM) was sampled by cascade impactors based on their aerodynamic diameter (dae, μm) and divided into size fractions: coarse (2.5 < dae), fine (0.25 < dae < 2.5) and ultrafine (<0.25). Size distributions of 20 priority PAHs adsorbed on these PM fractions were analyzed by gas chromatography coupled to tandem mass spectrometry in electron ionization (GC-EI-MS/MS). The total concentration of ∑20PAHs to which residents were exposed ranged from 0.09 ng/m3 to 47.18 ng/m3. A higher level of PAHs was detected in Ostrava (mean: 5.59 ng/m3) than in Ceske Budejovice (mean: 1.96 ng/m3). Statistically significant concentration differences between PAHs in individual seasons were observed in both sampled localities, with higher concentrations measured in winter than in summer. Fine and ultrafine particles predominated in the mass composition of the particulate matter. The ultrafine particle size contained 67–80% of total PAHs. Respiratory health risk was estimated based on inhalation cancer risk (ICR). Cancer risk attributable to personal inhalation exposure ranged from 2.8 × 10−8 to 4.3 × 10−4. In winter, higher cancer risk were found in Ostrava, mainly caused by a high concentration of carcinogenic PAHs bound to ultrafine particles. Overall, the personal monitoring data confirmed a higher air pollution burden in the industrial area and the winter season and highlighted the importance of focusing on ultrafine particles as the main carriers of potentially mutagenic and carcinogenic substances, such as PAHs. In addition, personal monitoring data provided more detailed and accurate information on individual-level exposures, revealing significant differences in exposure concentrations in people living in the same area.

Mono and polycyclic aromatic hydrocarbons in waterpipe wastewater: Level and ecotoxicological risk assessment

Increasing of tobacco consumption around the world has led to the production of a large volume of waterpipe wastewater that enter the environment (e.g., coastal areas)and threaten aquatic creatures. However, until now, no research has been carried out on the amounts of monocyclic and polycyclic aromatic hydrocarbons (PAHs) in hookah wastewater. In the current study, the levels of PAHs and BTEX compounds in waterpipe wastewater resulting from the use of different tobacco brands were determined and their eco-toxicological effects were also evaluated. The mean levels of ƩPAHs in waterpipe wastewater of Al Tawareg, Al-Fakher, Nakhla, Tangiers and traditional tobacco brands samples were 3.48 ± 1.65, 3.33 ± 1.52, 3.08 ± 1.25, 2.41 ± 0.87 and 0.70 ± 0.13 μg/L, respectively. The mean levels of ƩBTEX in waterpipe wastewater of Al Tawareg, Al-Fakher, Nakhla, Tangiers and traditional tobacco brands samples were also 2.53 ± 0.61, 2.65 ± 0.78, 2.51 ± 0.72, 2.35 ± 0.56, and 0.78 ± 0.12 μg/L, respectively. The maximum level of PAHs and BTEX compounds in all brands/flavors samples were for naphthalene (Naph) and toluene, respectively. The concentrations of some PAHs (fluoranthene (Flrt), anthracene (Ant), benzo(b)fluoranthene (BbF), benzo(b)fluoranthene (BkF), benzo (g,h,i)perylene (BghiP) and dibenzo (a, h) anthracene (DahA)) and BTEX compounds (benzene) in the waterpipe wastewater samples were more than recommended guidelines and standards by the international reputable organizations such as World Health Organization (WHO) for water quality. Waterpipe wastewater can be introduced as an important origin for the release of these dangerous contaminants into the environmental matrixes. Therefore, more stringent regulations should be considered for the safe disposal of such hazardous wastes including waterpipe wastewater.

Biomonitoring of polycyclic aromatic hydrocarbons exposure and short-time health effects in wildland firefighters during real-life fire events

Human biomonitoring data retrieved from real-life wildland firefighting in Europe and, also, worldwide are scarce. Thus, in this study, 176 Portuguese firefighters were biomonitored pre- and post- unsimulated wildfire combating (average:12–13 h; maximum: 55 h) to evaluate the impact on the levels of urinary polycyclic aromatic hydrocarbons hydroxylated metabolites (OHPAH; quantified by high-performance liquid chromatography with fluorescence detection) and the associated short-term health effects (symptoms, and total and differentiated white blood cells). Correlations between these variables and data retrieved from the self-reported questionnaires were also investigated. Firefighters were organized into four groups according to their exposure to wildfire emissions and their smoking habits: non-smoking non-exposed (NSNExp), non-smoking exposed (NSExp), smoking non-exposed (SNExp), and smoking and exposed (SExp). The most abundant metabolites were 1-hydroxynaphthalene and 1-hydroxyacenaphthene (1OHNaph + 1OHAce) (98–99 %), followed by 2-hydroxyfluorene (2OHFlu) (0.2–1.1 %), 1-hydroxyphenanthrene (1OHPhen) (0.2–0.4 %), and 1-hydroxypyrene (1OHPy) (0.1–0.2 %); urinary 3-hydroxybenzo(a)pyrene was not detected. The exposure to wildfire emissions significantly elevated the median concentrations of each individual and total OHPAH compounds in all groups, but this effect was more pronounced in non-smoking (1.7–4.2 times; p ≤ 0.006) than in smoking firefighters (1.3–1.6 times; p ≤ 0.03). The greatest discriminant of exposure to wildfire emissions was 1OHNaph + 1OHAce (increase of 4.2 times), while for tobacco smoke it was 2OHFlu (increase of 10 times). Post-exposure, white blood cells count significantly increased ranging from 1.4 (smokers, p = 0.025) to 3.7-fold (non-smokers, p < 0.001), which was accompanied by stronger significant correlations (0.480 < r < 0.882; p < 0.04) between individual and total OHPAH and total white blood cells (and lymphocytes > monocytes > neutrophils in non-smokers), evidencing the impact of PAH released from wildfire on immune cells. This study identifies Portuguese firefighters with high levels of biomarkers of exposure to PAH and points out the importance of adopting biomonitoring schemes, that include multiple biomarkers of exposure and biomarkers of effect, and implementing mitigations strategies.