Molecular Weight Polycyclic Aromatic Hydrocarbons Research Articles

Formation and biotoxicity of environmentally persistent free radicals in steelworks soil under thermal treatment

Thermal treatment are commonly used to address organic contaminated soils. In particular, the pyrolysis of organic substances can result in the creation of environmentally persistent free radicals (EPFRs). We investigated a steelworks site in Chongqing (China) to observe changes in EPFRs before and after thermal treatment. Our findings revealed that the EPFRs were carbon-centered radicals with a g-factor < 2.0030 and a spin density ranging from n.d.–5.23 × 1015 spins/mg. The formation of EPFRs was driving by polycyclic aromatic hydrocarbons (PAHs), Mn, Cu, and total organic carbon (TOC). Following the thermal treatment, the spin densities of EPFRs increased by a factor of 0.25 to 1.81, with maximum levels reached at 300 °C. High molecular weight PAHs exhibited high heat capacity, enabling the generation of more EPFRs. The thermal decay of EPFRs occurred in two stages, with the shortest 1/e lifetime lasting up to 16.8 h. Raising the temperature or prolonging time can significantly reduce EPFRs levels. Thermal treatment increased the generation of EPFRs, hydroxyl radicals (•OH) and superoxide radical (•O2–), leading to a decrease in bacterial luminescence. Specifically, •OH contributed to approximately 73% of the B. brilliantus inhibition. Our results highlight that the thermal treatment significantly enhance EPFRs concentrations, and the treated soil remained ecologically risky. The knowledge of the formation of EPFRs and their biotoxicity is shedding new light on the thermal treatment risk management.

Biochars assisted phytoremediation of polycyclic aromatic hydrocarbons contaminated agricultural soil: Dynamic responses of functional genes and microbial community

A biochar-intensified phytoremediation experiment was designed to investigate the dynamic effects of different biochars on polycyclic aromatic hydrocarbon (PAH) removal in ryegrass rhizosphere contaminated soil. Maize and wheat straw biochar pyrolyzed at 300 °C and 500 °C were amended into PAH-contaminated soil, and then ryegrass (Lolium multiflorum L.) was planted for 90 days. Spearman's correlations among PAH removal, enzyme activity, abundance of PAH-ring hydroxylating dioxygenase (PAH-RHDα), and fungal and bacterial community structure were analyzed to elucidate the microbial degradation mechanisms during the combined remediation process. The results showed that 500 °C wheat straw biochar had higher surface area and more nutrients, and significantly accelerated the phytoremediation of PAHs (62.5 %), especially for high molecular weight PAH in contaminated soil. The activities of urease and dehydrogenase and the abundance of total and PAH-degrading bacteria, which improved with time by biochar and ryegrass, had a positive correlation with the removal rate of PAHs. Biochar enhanced the abundance of gram-negative (GN) PAH-RHDα genes. The GN PAH-degraders, Sphingomonas, bacteriap25, Haliangium, and Dongia may play vital roles in PAH degradation in biochar-amended rhizosphere soils. Principal coordinate analysis indicated that biochar led to significant differences in fungal community structures before 30 days, while the diversity of the bacterial community composition depended on planting ryegrass after 60 days. These findings imply that the structural reshaping of microbial communities results from incubation time and the selection of biochar and ryegrass in PAH-contaminated soils. Applying 500 °C wheat straw biochar could enhance the rhizoremediation of PAH-contaminated soil and benefit the soil microbial ecology.

Variations of the atmospheric polycyclic aromatic hydrocarbon concentrations, sources, and health risk and the direct medical costs of lung cancer around the Bohai Sea against a background of pollution prevention and control in China

Abstract. The Bohai Sea (BS) region, an area of China that is severely polluted with atmospheric polycyclic aromatic hydrocarbons (PAHs), has received wide attention in recent decades. To characterize the variations of the concentrations and sources of PAHs from June 2014 to May 2019, 15 PAH congeners (Σ15PAHs) were measured in atmospheric samples (N = 228) collected at 12 sites around the BS, and the health risk and direct medical costs associated with lung cancer caused by exposure to PAHs were also estimated. The annual daily average concentration of Σ15PAHs was 56.78 ± 4.75 ng m−3, which was dominated by low molecular weight PAHs (LMW-PAHs) containing three rings (58.7 ± 7.8 %). During the 5-year sampling period, the atmospheric Σ15PAHs concentration reduced by 17.5 % for the whole BS region, with an especially large drop of 51.7 % observed in the tightly controlled area of Tianjin (TJ), which was mainly due to a decrease in the concentration of high molecular weight PAHs (HMW-PAHs) containing five or six rings. Generally, the concentration of Σ15PAHs was highest in winter and lowest in summer, which can mainly be attributed to the change in LMW-PAH concentration. Based on the positive matrix factorization (PMF) model, PAHs in the BS region were mainly ascribed to coal combustion and biomass burning. The PAH contributions of coal combustion and motor vehicles showed different trends for the BS region (PAHs from coal combustion rose by 7.2 % and PAHs from motor vehicles fell by 22.4 %) and for TJ (PAHs from coal combustion fell by 12.6 % and PAHs from motor vehicles rose by 6.9 %). The incidence of lung cancer (ILCR) caused by exposure to atmospheric PAHs decreased by 74.1 % and 91.6 % from 2014 to 2018 in the BS region and in TJ, respectively. This was mainly due to the decrease in the concentration of highly toxic HMW-PAHs and was reflected in USD 10.7 million of savings in direct medical costs of lung cancer caused by exposure to PAHs, which represent a decrease of 46.1 % compared to the corresponding costs before air pollution prevention and control was implemented around the BS. There was an even higher reduction in medical costs of 54.5 % in TJ. Hence, this study proves that implementing pollution prevention and control not only effectively reduced the concentration of pollutants and the risks caused by them, but it also significantly reduced the medical costs of diseases caused by the corresponding exposure.

Assessment of particulate PAHs toxicity from alcohol-diesel blends fuelled high compression ratio CI engine

Transport and power generation applications will play an important role in current and next-generation compression ignition (CI) engines. Methanol, ethanol, and butanol have emerged as potential alternative fuels for internal combustion engines capable of reducing overall greenhouse gases (GHG) and pollutant emissions. This study deals with the morphological characterization of particulate matter (PM) and toxicity assessment of polycyclic aromatic hydrocarbons (PAHs) for methanol, ethanol and butanol blending with diesel, and provides new findings and results in the specific literature. It defines new limits of alcohol fractions in diesel blends for their applications in CI engines. For the experimental assessment, a single-cylinder CI engine was used with an increased compression ratio (CR) from 17.5 to 26. Alcohol fraction of 20% (v/v) in diesel reduced the PM emissions in the range of 29–38% than diesel. PM was further reduced, up to ∼50%, for higher ethanol and butanol fractions (∼50%), and the soot morphological characteristics exhibit smaller particle sizes (400–600 nm) than diesel (up to 2 μm). Moreover, 20% of alcohol fraction led to a 34–60% reduction in PAHs. The toxicity evaluation of the tested alcohol-diesel blend indicates that high molecular weight PAHs and nitro-PAHs are the main contributors to the overall toxicity. Benzo[a]pyrene and dibenzo-anthracene were the prominent PAHs. Increasing the alcohol blend ratio significantly reduced the toxicity potential, ranging from 20 to 67%.

Polycyclic aromatic hydrocarbons in coastal rivers in Jiangsu Province, China: Spatial distribution, source apportionment and human impacts

The ocean is the ultimate sink for all pollutants, rivers are important channels for land-based pollutants to enter the oceans. Riverine transport of polycyclic aromatic hydrocarbons (PAHs) to coastal seas in China poses environmental threats. This study examined the spatial and temporal distribution of PAHs in coastal rivers in Yancheng City in Jiangsu Province of China, with the aim of identifying their likely sources, concentrations, and influencing factors. Surface sediments were taken from the Xinyanggang River (XYR) and the Sheyang River (SYR). The concentrations of Ʃ16PAHs in river sediments were measured on average 477.05 ng/g dry weight (dw), with values varying from 2.18 to 6351.42 ng/g, indicating a moderate pollution level, with a dominance of high molecular weight (HMW) PAHs. The XYR exhibited significantly higher PAHs concentrations compared to the SYR. The key sources of PAHs were vehicle emissions (47.87%), coal and natural gas combustion (35.07%). Geographically weighted regression and redundancy analysis linked PAHs pollution to distinct land use patterns and socioeconomic indicators, highlighting urban land as the major contributor, driven by high urbanization and industrialization (70.91%). In XYR, industrial activities and transport emissions were major contributors, while in SYR, agricultural activities predominantly influenced PAHs pollution. Urgent mitigation strategies are needed to reduce PAHs pollution in river sediments, mitigating ecological and human risks associated with these contaminants.

Levels and sources of polycyclic aromatic hydrocarbons (PAHs) near hospitals and schools using leaves and barks of Sambucus nigra and Acacia melanoxylon

Polycyclic aromatic hydrocarbons (PAHs) are among the most studied organic compounds in urban environments, due to their known threat to human health. This study extends the current knowledge regarding the ability of different vegetative parts of different tree species to accumulate PAHs. Moreover, exposure intensity to PAHs in areas frequented by population susceptible to adverse health effects of air pollution is evaluated. For this, leaves and barks of Sambucus nigra (S. nigra) and Acacia melanoxylon (A. melanoxylon) were collected at urban areas in the Andean city of Quito, at seven points near hospitals and schools. A methodology, previously developed, for the extraction, purification, and quantification of PAHs associated with the leaves and bark of S. nigra was employed and also validated for leaves and bark of A. melanoxylon. The total PAH level varied from 119.65 ng g−1 DW (dry weight) to 1969.98 ng g−1 DW (dry weight) with naphthalene (Naph), fluoranthene (Flt), pyrene (Pyr), chrysene (Chry), and benzo[a]pyrene (BaP) predominating in all samples. The results indicate that the leaves and bark of tree species studied have certain abilities to bio-accumulate PAH according to their molecular weight. The leaves of S. nigra and bark of A. melanoxylon showed the highest ability to accumulate PAHs, mainly those with high and medium molecular weight, respectively. The highest incidence of light molecular weight PAHs was found in the leaves of A. melanoxylon. Furthermore, coal combustion, biomass burning, and vehicle emissions were identified as the main PAHs sources. Concentrations of PAHs associated with tree species suggest an affectation in areas frequented by populations susceptible to air pollution. This fact shows the importance of regulatory scheme to significantly improve the air quality in the city integrating a knowledge-based decision-making.

Benzo(k)fluoranthene and benzo(b)fluoranthene degradation by Selenastrum capricornutum and identification of metabolites using HPLC-FD and HPLC-ESI-QqQ-MS/MS

Selenastrum capricornutum efficiently degrades high molecular weight polycyclic aromatic hydrocarbons (HMW PAHs). Until now, there are few studies on the benzo(k)fluoranthene (BkF) and benzo(b)fluoranthene (BbF) biodegradation by this microalga. For this reason, in the present work, extracts obtained from cultures of S. capricornutum were incubated with BkF and BbF individually, and analyzed by HPLC with fluorescence and different mass spectrometry detection modes: i) the HPLC-ESI(+)-MS/MS (MRM mode) analysis that confirmed the formation of monohydroxylated and dihydrodiol metabolites indicating that these PAHs could be simultaneously degraded through the monooxygenase and dioxygenase; ii) HPLC-ESI(+)-MS (full scan mode) that showed the formation of key metabolites containing four and two aromatic rings possibly resulting from aromatic ring-opening oxygenases, not known until now in microalgae; iii) HPLC-FD analysis that confirmed the individual BkF and BbF degradation occurring in extra- and intra-cellular extracts, indicating that an oxygenase enzyme complex is released by microalgae cells to the external environment to perform HMW PAHs biodegradation. So, this work presents new insights into the metabolic pathways of BkF and BbF biodegradation by S. capricornutum; likewise, the intra- and extra-cellular extracts of this microalgae have great potential to be applied in environmental procedures.

Hydrocarbon-based parameters for the identification of oil contamination in an area with brown coal mining: Emphasis on pyrogenic index and alkylated PAHs

The aim of the study was to propose hydrocarbon-based parameters that can ben used to identify oil derived contamination in an area with a long-term load of coal mining industry. Aliphatic hydrocarbons and PAHs have been quantified for bottom sediments in the Bílina River, Czechia. Presented data demonstrate that all river sediments are highly contaminated with PAHs. The results showed that the distribution of PAHs was not possible to interpret by using the standard evaluation due to multisource long-term sedimentation of petroleum by-products, coal tars, and accidents of processing industry in the river system. The presence of petroleum derived hydrocarbons has been initially screened by the bulk parameter TEH and confirmed by the occurrence of steranes, hopanes and the unresolved complex mixture (UCM) in the chromatograms. The identification of the biomarkers 25-Norhopane and Gammacerane point out onsite microbial degradation of parent hydrocarbon compounds. The interpretation of the ratios Fl/Py, An/P, BaAn/Ch were not decisive to prove petrogenic origin of PAHs in the river sediments. However, using the combined evaluation of TEH together with the ratio of low molecular over high molecular weight PAHs, pyrogenic index and the presence of specific oil derived biomarkers allowed to prove the presence of petroleum contamination. Environmental implicationDue to oil spill accidents and intensive coal mining over the years, polycyclic aromatic hydrocarbons (PAHs) have been present in extreme amounts in bottom sediments of a tributary of the Elbe River, so called the Bílina River. Due to its hydrophobic and carcinogenic character, mutual understanding of the fate of alkylated PAHs homologues are usually overlooked within EPA PAHs 16 monitoring programme. This study pays attention to alkylated PAHs homologues and conventional diagnostic ratios when identifying oil derived contamination.

Removal of PAHs in paddy fields: How natural periphytic biofilm enhances the removal process and the mechanisms involved

Previous studies on the removal of polycyclic aromatic hydrocarbons (PAHs) from farmland have mostly relied on anthropogenic biotic or abiotic amendments. Here, an indigenous paddy periphytic biofilm (PB) composed of complex symbolic communities was enriched, and its essential role, as well as the potential mechanisms of PAHs dissipation, was investigated. A pot experiment revealed that PB achieved 92.87% and 92.76% removal of the USEPA priority PAHs from the overlying water and soil of a heavily PAHs-contaminated paddy field, respectively. This subsequently decreased ΣPAHs accumulation in rice shoots to 4.12 ± 1.08 ng g-1, under the thresholds based on food safety standards. The physiology of PB in an aquatic culture with PAHs was assessed to understand the toxicity and removal mechanism. Extracellular polymeric substances (EPS) adsorption occurred in the early stage, followed by late biodegradation, which was considered the primary mechanism for removing PAHs. In this process, the PB contributed more to the high molecular weight PAHs compared to the low molecular weight. Furthermore, 16S-rRNA sequencing demonstrated specific functional phyla (Proteobacteria, Ascomycota, and Chloroplastida) with significantly higher relative abundances in periphytic communities with PAHs, which facilitated PAHs degradation. The predicted synergetic metabolic pathway involved 33 PAHs-degrading genes as inferred by PICRUSt. These findings suggest that PB could provide a promising strategy for target PAHs remediation in situ and food safety in contaminated paddy fields.

Biodegradation of pyrene during submerged cultivation of Trametes versicolor

Pyrene is one of the most persistent pollutants belonging to the group of high molecular weight polycyclic aromatic hydrocarbons. Due to the presence of fused benzene rings these compounds are extremely difficult for biodegradation. The white-rot fungi possess remarkably high potential when it comes to the biodegradation of toxic organic substances with aromatic rings due to their unique lignin-degrading enzymatic complex. In the present study, pyrene with concentrations up to 200 ppm was added to the nutrient medium during submerged cultivation of the higher basidiomycete mushroom Trametes versicolor NBIMCC 8939. The experiment continued for 20 days and samples were taken every 5 days. Analysis of the activities of the enzymes laccase and manganese-dependent peroxidase were performed as well as determination of the residual pyrene concertation and identification of the by-products of the degradation process. It was established that the highest pyrene removal was achieved when the lowest initial concentration was introduced to the medium. The strain T. versicolor NBIMCC 8939 was able to biodegrade 12% of the initially introduced 50 ppm pyrene in the medium.

A 150 years record of polycyclic aromatic compounds in the Sihailongwan Maar Lake, Northeast China: impacts of socio-economic developments and pollution control.

The geochemical composition of sediment cores can serve as a proxy for reconstructing past human and nature-driven environmental and climatic changes. We investigated the temporal variation in the concentrations and fluxes of polycyclic aromatic compounds (PACs) which include polycyclic aromatic hydrocarbons (PAHs), oxygenated PAHs, and azaarenes in the Sihailongwan Maar Lake and found that they remained low before 1950. The PAC concentrations and fluxes increased substantially since 1950, which was in good agreement with the fast socio-economic development, industrialization, and associated growth in fossil fuel consumption in China, particularly since the 1980s. After 2010, the PAC fluxes decreased, which was consistent with the implementation of air pollution control policies in China at that time. The concentration ratios of the sums of low to high molecular weight PAHs (LMW-PAHs/HMW-PAHs), benzo[e]pyrene/benzo[a]pyrene, and benzo[a]anthracene-7,12-dione/benzo[a]anthracene all decreased from bottom to top of the sediment core, reflecting the rapidly increasing contribution of emissions derived from high-temperature fossil fuel combustion (energy, transport and industry) to the PAC emissions in recent times at the expense of biomass burning. In addition, these data reflect the increasing local sources of PACs in more recent times because of the enhanced human activities in the area surrounding the Maar lake. Our results demonstrate that PAC fluxes and concentrations in sediment cores reflect the regional and national economic development and the efficiency of pollution control measures.

Polycyclic aromatic hydrocarbons in silicone wristbands of Uruguayan children: measurement and exposure source exploration.

Polycyclic aromatic hydrocarbons (PAHs) pose health risks to children, potentially resulting in stunted growth, obesity, and cognitive deficits, but lack of reliable and noninvasive means to measure PAHs results in poor understanding of exposure patterns and sources in this vulnerable population. In this study, 24 children aged ∼7 years (9 boys and 15 girls) from Montevideo, Uruguay wore silicone wristbands for 8 days to monitor the exposure of 27 PAHs. Wristbands were extracted using a modified ethyl acetate tandem solid phase extraction clean up and then analyzed via gas chromatography with tandem mass spectrometry. This analysis has reported LODs for 27 PAHs between 0.05 and 3.91 μg L-1. Eighteen PAHs were detected in >50% of the samples with concentration medians ranging 1.2-16.3 ng g-1 of wristband. Low molecular weight PAHs (2-3 rings) such as naphthalene and its alkyl derivatives were highly correlated (0.7-0.9) in the wristbands, suggesting exposure from related sources. Exposure source exploration focused on secondhand tobacco smoke, potentially through caregivers who reported on smoking habits in an associated survey. A principal components analysis (PCA) was conducted to examine patterns in PAH compounds detected in the wristbands; subsequently, the resulting components were compared according to current smoking among caregivers. The PCA analysis revealed a grouping of participants based on higher exposure of 1-methyl naphthalene, pyrene, fluoranthene, 1-methylphenanthrene, dibenzothiophene and 2-phenyl naphthalene. The derived components did relate with parental smoking, suggesting that some participants experienced exposure to a common source of certain PAHs outside of parental smoking. This is the first study to assess PAH exposure in young children from South America. Using wristbands, our study indicates exposure to multiple, potentially harmful chemicals. Wristbands could provide a comprehensive picture of PAH exposure in children, complementing other non-invasive biomonitoring approaches.

Quantitative characterization of resident’ exposure to typical semi-volatile organic compounds (SVOCs) around a non-ferrous metal smelting plant

To comprehensively characterize residents’ exposure to major semi-volatile organic compounds (SVOCs), samples of indoor floor wipes, size-segregated airborne particles, gaseous air, food, and paired skin wipes were simultaneously collected from residential areas around a large non-ferrous metal smelting plant as compared with the control areas, and three typical SVOCs (including polychlorinated biphenyls (PCBs), polycyclic aromatic hydrocarbons (PAHs), and halogenated PAHs (HPAHs)) were determined. Comparison and correlation analysis among matrices indicated PAHs were the major contaminants emitted from metal smelting activities compared to HPAHs and PCBs, with naphthalene verified as the most important characteristic compound, and their accumulation on skin may be a comprehensive consequence of contact with floor dust and air. While patterns of human exposure pathways for the SVOCs were found to be clearly correlated to their vapor pressure, dermal absorption was the major contributor (51.1–76.3%) to total carcinogenic risk (TCR) of PAHs and HPAHs for surrounding residents, especially for low molecular weight PAHs, but dietary ingestion (98.6%) was the dominant exposure pathway to PCBs. The TCR of PAHs exceeded the acceptable level (1 × 10−4), implying smelting activities obviously elevated the health risk. This study will serve developing pertinent exposure and health risk prevention measures.

Assessing the ecological impacts of polycyclic aromatic hydrocarbons petroleum pollutants using a network toxicity model

Polycyclic aromatic hydrocarbons (PAHs) are significant petroleum pollutants that have long-term impacts on human health and ecosystems. However, assessing their toxicity presents challenges due to factors such as cost, time, and the need for comprehensive multi-component analysis methods. In this study, we utilized network toxicity models, enrichment analysis, and molecular docking to analyze the toxicity mechanisms of PAHs at different levels: compounds, target genes, pathways, and species. Additionally, we used the maximum acceptable concentration (MAC) value and risk quotient (RQ) as an indicator for the potential ecological risk assessment of PAHs. The results showed that higher molecular weight PAHs had increased lipophilicity and higher toxicity. Benzo[a]pyrene and Fluoranthene were identified as core compounds, which increased the risk of cancer by affecting core target genes such as CCND1 in the human body, thereby influencing signal transduction and the immune system. In terms of biological species, PAHs had a greater toxic impact on aquatic organisms compared to terrestrial organisms. High molecular weight PAHs had lower effective concentrations on biological species, and the ecological risk was higher in the Yellow River Delta region. This research highlights the potential application of network toxicity models in understanding the toxicity mechanisms and species toxicity of PAHs and provides valuable insights for monitoring, prevention, and ecological risk assessment of these pollutants.

Air‐Sea Gas Exchange and Its Potential Influence on the Regional Fate of Polycyclic Aromatic Hydrocarbons in the East China Marginal Sea

AbstractTo investigate the air‐sea gas exchange and its potential influence on the regional fate of polycyclic aromatic hydrocarbons (PAHs) in the East China Marginal Seas (ECMS), which consist of the East China Sea (ECS) and Yellow Sea (YS), we collected air and surface seawater samples of this area in the summer 2018 and winter 2019, respectively. Generally, PAHs underwent a strong volatilization process in the ECMS in both summer and winter. Good correlations between wind speed and the magnitude of air‐sea gas exchange were found for low molecular weight PAHs, suggesting the rate of their air‐sea gas exchange was influenced by the static stability of overlying atmosphere. However, such an influence for high molecular weight PAHs was constrained by their low Henry's law constant. Dissolved concentration of PAHs in surface seawater was another key factor regulating their air‐sea gas exchange, which not only influenced the rate of air‐sea gas exchange but also was involved in the exchange direction. Higher air‐sea gas exchange fluxes of PAHs in winter were attributed to their increasing dissolved concentrations in seawater during this season. A mass conservation analysis revealed a huge volatilization loss of PAHs from seawater to atmosphere, suggesting air‐sea gas exchange might be a key process to modulate the distribution and occurrence of PAHs in the ECS and YS. Such a loss of PAHs in seawater might be compensated by the sediment resuspension, which implied that the sedimentary deposit could serve as a secondary source of PAHs in seawater and overlying atmosphere.

Polycyclic Aromatic Hydrocarbons (PAHs) in aquatic ecosystem exposed to the 2020 Baghjan oil spill in upper Assam, India: Short-term toxicity and ecological risk assessment.

This study focuses on the short-term contamination and associated risks arising from the release of Polycyclic Aromatic Hydrocarbons (PAHs) due to the 2020 Baghjan oil blowout in upper Assam, India. Shortly after the Baghjan oil blowout, samples were collected from water, sediment, and fish species and examined for PAHs contents. The results of the analysis revealed ΣPAHs concentrations ranged between 0.21-691.31 μg L-1 (water); 37.6-395.8 μg Kg-1 (sediment); 104.3-7829.6 μg Kg-1 (fish). The prevalence of 3-4 ring low molecular weight PAHs compounds in water (87.17%), sediment (100%), and fish samples (93.17%) validate the petrogenic source of origin (oil spill). The geographic vicinity of the oil blowout is rich in wildlife; thus, leading to a significant mass mortality of several eco-sensitive species like fish, plants, microbes, reptiles, amphibians, birds and mammals including the Gangetic River dolphin. The initial ecological risk assessment suggested moderate to high-risk values (RQ >1) of majority PAHs concerning fish, daphnia, and algae species. This study highlights the need for recognizing the potential for short-term exposure to local species. To safeguard local ecosystems from potential future environmental disasters, it is imperative for the government to adopt a precautionary strategy.

Unravelling mixed sources of polycyclic aromatic hydrocarbons (PAH) in urban soils by visual characterization of anthropogenic substrates and coal particles, 71 PAH and alkylated PAH patterns

The identification of polycyclic aromatic hydrocarbon (PAH) sources in heterogeneous urban soils containing pyrogenic and/or petrogenic anthropogenic substrates is a common task for risk assessment. Here, for the first time, the results of source identification using analysis of 71 PAH, alkylated PAH patterns and PAH Alkylation Index were related to visually identified and quantified anthropogenic substrates in 50 soil samples. Only the combination of chemical methods with visual characterization enabled the deeper understanding of varying alkylated PAH patterns used for source apportionment and their superimposition if multiple sources occur. Pyrogenic substrates show homogenic slope-shape PAH patterns despite large visual variety. Petrogenic substrates (bituminous coals), show prevailingly bell-shape patterns but pyrogenic patterns also occur, probably due to residues from industrial processes and/or sorption of other pyrogenic PAH. Superimposition of both PAH patterns within a sample results in intermediate patterns, which are determined by the abundance of substrates and their individual PAH contents. A discrepancy between the share of petrogenic substrates and petrogenic PAH was observed due to low-medium PAH contents from coals/tailings. This may lead to misinterpretations if only chemical source identification methods are applied. With increasing proportion of petrogenic PAH in the mixture, the intermediate V-shape pattern (later bell-shape) appears in lower molecular weight PAH and moves progressively to higher molecular weight PAH. ∑71 PAH contents vary from 1.77 to 326.5 mg/kg (median 26.5 mg/kg). Non-EPA PAH measured include highly toxic ∑4 dibenzopyrene isomers (0.045–6.23 mg/kg, median 0.79 mg/kg) and 7H-benzo[c]fluorene (0.008–1.57 mg/kg, median 0.12 mg/kg). Most common anthropogenic substrates are bottom ashes, slags, bituminous coals/tailings and coke/coke ash. The PAH Alkylation Index identifies reliably samples dominated by either petrogenic (<0.4) or pyrogenic (>0.9) PAH, independently of the PAH content. Mixed or primarily pyrogenic PAH sources (0.4–0.9) need further investigations, like the presented combination of methods, which enables a reliable source apportionment.

Analysis of persistent organic pollutants and heavy metals in mysticetes from the United Arab Emirates

Chemical pollution is a major threat that can increase the mortality and lower the reproductive success of cetaceans. In this study we assess, for the first time, the level of contamination of selected priority pollutants consisting of polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), polycyclic aromatic hydrocarbons (PAHs) and heavy metals in whales found stranded in the United Arab Emirates. The samples included five Bryde’s whales (Balaenoptera edeni) and one humpback whale (Megaptera novaeangliae) from the Arabian Gulf and one blue whale (Balaenoptera musculus) from the Gulf of Oman. None of the 18 OCPs tested for were detected. Of the 20 PCB congeners tested for, only one was detected in two (40%) Bryde’s whales.The concentrations of trace elements and heavy metals were lower than reported in baleen whales from the southern hemisphere. PAHs, the predominant pollutants in this study, were detected in the tissues of all examined specimens. The predominance of low molecular weight PAHs over high molecular weight PAHs suggests that PAH exposure may have been primarily from petrogenic sources. The amputation of the tail fluke in one case and bruising of a second whale suggest trauma and marine debris entanglement may have contributed to death in at least two cases. We observed no evidence of marine debris ingestion when such examinations were possible

Status, Source, and Risk Assessment of Heavy Metal(Loid)s and Polycyclic Aromatic Hydrocarbons (PAHs) in the Street Dust of Ilam, Iran

A total of 25 Ilam street dust specimens were sampled to investigate the possible ecological and health risks of heavy metal(loid)s and polycyclic aromatic hydrocarbons (PAHs). We found that the average concentrations of heavy metal(loid)s, namely Pb, Zn, Cu, Cr, Cd, Ni, V, and As, were 52, 213, 63, 46, 0.4, 44, 31, and 5 mg/kg, respectively. The average concentration of all heavy metal(loid)s except for Cr and V was several times higher than the baseline values. We evaluated Zn and Pb in the region using the average enrichment factor (EF) and pollution index (PI); the Nemerow integrated pollution index (NIPI) indicated that 76% of the samples had high degrees of pollution. According to principal component analysis (PCA), three principle components are involved in the heavy metal(loid) pollution of Ilam street dust. For example, the pollution sources of Cu, Cr, Cd, and Ni likely originated from anthropogenetic origins, including traffic, tire depreciation, and gasoline use. The sources of Pb and Zn were other anthropogenic activities, such as metal corroding and the combustion of garbage and gases from industries, while V and As were probably from natural sources. The range of sum over 11 PAHs was 167–11,497 μg/kg with a mean of 2242 μg/kg. The concentration of low molecular weight (LMW) PAHs averaged 1471 μg/kg, accounting for 66% of the total PAHs; their sources were mainly associated with combustion and pyrogenic emissions. The PCA also revealed that PAHs mainly originated from burning fossil fuels. The values of RQ∑PAHs (MPCs) and RQ∑PAHs (NCs) were respectively >1 and ≥800, indicating a high ecosystem risk for PAHs. Mean values for RQ∑PAHs (MPCs) and RQ∑PAHs (NCs) were 4 and 1021, respectively, implying that Ilam street dust poses a relatively high ecosystem risk of PAHs. Street dust PAHs’ toxic equivalency quotient (TEQ) varied from 26 to 199 μg/kg. The total cancer risk was 3.92 × 10−4 and 4.06 × 10−4 for adults and children, respectively, indicating that the potential for cancer risk is very high through dust dermal contact and ingestion.

Distribution, composition and risk assessment of hydrocarbon residue in surficial sediments of El-Dakhla, El-Kharga and El-Farafra oases, Egypt.

This work examined the polycyclic aromatic hydrocarbons (PAHs) and n-alkanes quantities, sources, and hazards in sediments collected from the Egyptian Western Desert Oases namely: Dakhla, Kharga and Farafra oases. The n-alkane (C9-C20) residue concentrations have ranged from 0.66 to 2417.91 µg/g recorded for the three Oases. On the other hand, the total n-alkane ranged from 448.54 µg/g to 8442.60 µg/g. Higher carbon preference index (CPI) values (> 1.0) proposed that the natural sources could be the main contributor to n-alkanes in the Oases sediment. GC-MS/MS (selected reaction monitoring (SRM) method) was used for the determination of the ΣPAHs concentrations in the studied sediments. The ΣPAHs concentrations (ng/g, dry weight) in the studied three Oases varied from 10.18 to 790.14, 10.55 to 667.72, and from 38.27 to 362.77 for the Kharga, Dakhla and Farafra Oases, respectively. The higher molecular weight PAHs were the most abundant compounds in the collected samples. Assessing potential ecological and human health issues highlighted serious dangers for living things and people. All the investigated PAHs had cancer risk values between 1.43 × 10-4 and 1.64 × 10-1, this finding suggests that PAHs in the samples under study pose a moderate risk of cancer. The main sources of PAHs in this study are biomass, natural gas, and gasoline/diesel burning emissions.