Abundant Polycyclic Aromatic Hydrocarbons Research Articles

Total and bioavailable polycyclic aromatic hydrocarbons in unused and operated heat-not-burn tobacco products and conventional cigarettes

Tobacco product waste poses a global environmental issue, affecting urban and coastal areas alike. The present studies report, for the first time, the total and bioavailable polycyclic aromatic hydrocarbons (PAHs) concentrations in unused and operated heat-not-burn (HnBs) tobacco products. To enable direct comparisons, identical sets of studies were conducted using conventional cigarettes (CCs). Five low-molecular PAHs were determined in HnBs at total concentrations that were of the same order before and after operation (Σ5PAH = 47.37 ± 3.44 ng unit−1 and Σ5PAH = 69.36 ± 5.78 ng unit−1 in unused and used HnBs, respectively). The incomplete combustion of organics during smoking of CCs, yielded substantially higher amounts of PAHs with their sum (Σ10PAHs = 1449 ± 113 ng unit−1) being >20 times larger than those in HnBs. The tobacco and filter were the most contaminated parts in HnBs. In unused CCs, tobacco had the highest PAHs load and after smoking, the spent filter was the most contaminated part, containing ∼80% of the total amount of PAHs. Naphthalene was the most abundant PAH detected in all tobacco products. Despite the high total PAH concentrations found in smoked CCs, the sums of the bioavailable PAH concentrations were of the same order in all tested tobacco products (Σ5PAH = 61.38 ± 1.79 ng unit−1 in unused HnBs, Σ5PAH = 70.87 ± 7.67 ng unit−1 in used HnBs, Σ4PAH = 66.92 ± 5.95 ng unit−1 in unused CCs, and Σ6PAH = 47.94 ± 1.26 ng unit−1 in smoked CCs). This finding was related to smoking affecting PAHs’ leachability from CCs and delaying their desorption from the solid matrix. Adjusting the pH, salt and humic acids content at environmentally relevant values did not affect PAHs leaching at 24 h of soaking. Finally, the leaching behavior of PAHs in natural waters (river water, rainwater, and seawater) was found similar to that in ultrapure water, experimentally verifying the ability of tobacco product waste to leach PAHs into the aquatic environment.

Influence of hydrothermal asteroidal conditions on the molecular structure and isotopic compositions of polycyclic aromatic hydrocarbons

A variety of polycyclic aromatic hydrocarbons (PAHs) are reported in carbonaceous chondrites (CCs) and in the interstellar medium (ISM). Although PAHs in CCs are not as large as those detected in the ISM, their carbon isotope composition is interpreted as pinpointing an interstellar origin. In contrast, their hydrogen isotope composition can be related to the extent of secondary processes, as is the proportion of alkylated PAHs within CCs. Here, we experimentally investigate the molecular and isotopic evolution of PAHs under simulated asteroidal hydrothermal conditions at 150 °C. Results show that PAHs are chemically stable under these conditions whatever their size, i.e. no destruction, conjugation nor alkylation occurs, even in the presence of other reactive organic molecules. Plus, PAHs retain their carbon isotope compositions even in the presence of another carbon-rich reservoir, either organic or inorganic. On the other hand, their hydrogen isotope composition is modified through exchange with water. Of note, as shown by additional experiments, the presence of smectites, abundant in CCs, impacts the relative abundances of extractable PAHs, saponite trapping more efficiently the larger PAHs. Altogether, results of the present experiments show that PAHs of CCs can be used as tracers of both pre-accretion and secondary processes.

Health Risk Assessment of Polycyclic Aromatic Hydrocarbons from Cooking Fuels burning in Nigeria

Cooking activities are an important source of indoor air pollution which contributes significantly to Polycyclic Aromatic Hydrocarbons (PAHs) in the environment. This study investigated sixteen (16) priority PAHs emitted from smoke in eight (8) cooking fuels commonly used in Nigeria. Gas Chromatography Mass Spectrometry (GC-MS) was used for sample analysis and the potential health risk associated with exposure to PAHs were evaluated. The highest total quantified PAHs concentration was obtained from the burning of palm kernel fiber with an average ΣPAHs of 14.06 mg/kg. The result showed a variation in the average concentration of 10.82 − 14.06 mg/kg for all the cooking fuels. 3-ringed PAHs were found to be the dominant PAHs in the samples considered in terms of concentrations and frequency of occurrence at 7.03-9.42 mg/kg. Benzo[a]anthracene was the most abundant PAHs in biomass materials while Benzo[a]pyrene was the most abundant in liquified petroleum gas and Benzo[b]fluoranthene in kerosene. The cancer risk for both the children and adult obtained for all the cooking fuel samples were less than 10 − 6 which is satisfactory except in sawdust which has a value of 1.30 × 10 − 5 and 1.44 × 10 − 5 for child and adult, respectively. It is recommended that cleaner cooking fuels be used in well-ventilated environments to reduce exposure to these pollutants. Highlights Sixteen priority PAHs in emissions from the burning of eight cooking fuels in Nigeria were investigated Emission sources of the PAHs were identified using diagnostic ratios Health risks of PAHs in emissions from the burning of cooking fuels is higher in adult

Impact of Potentially Toxic Compounds in Cow Milk: How Industrial Activities Affect Animal Primary Productions.

Potentially toxic elements (PTEs) and polycyclic aromatic hydrocarbons (PAHs) frequently coexist in soils near industrial areas and sometimes in environmental compartments directly linked to feed (forage) and food (milk) production. However, the distribution of these pollutants along the dairy farm production chain is unclear. Here, we analyzed soil, forage, and milk samples from 16 livestock farms in Spain: several PTEs and PAHs were quantified. Farms were compared in terms of whether they were close to (<5 km) or far away from (>5 km) industrial areas. The results showed that PTEs and PAHs were enriched in the soils and forages from farms close to industrial areas, but not in the milk. In the soil, the maximum concentrations of PTEs reached 141, 46.1, 3.67, 6.11, and 138 mg kg-1 for chromium, arsenic, cadmium, mercury, and lead, respectively, while fluoranthene (172.8 µg kg-1) and benzo(b)fluoranthene (177.4 µg kg-1) were the most abundant PAHs. Principal component analysis of the soil PTEs suggested common pollution sources for iron, arsenic, and lead. In the forage, the maximum contents of chromium, arsenic, cadmium, mercury, and lead were 32.8, 7.87, 1.31, 0.47, and 7.85 mg kg-1, respectively. The PAH found in the highest concentration in the feed forage was pyrene (120 µg kg-1). In the milk, the maximum PTE levels were much lower than in the soil or the feed forages: 74.1, 16.1, 0.12, 0.28, and 2.7 µg kg-1 for chromium, arsenic, cadmium, mercury, and lead, respectively. Neither of the two milk samples exceeded the 20 µg kg-1 limit for lead set in EU 1881/2006. Pyrene was the most abundant PAH found in the milk (39.4 µg kg-1), while high molecular weight PAHs were not detected. For PTEs, the results showed that soil-forage transfer factors were higher than forage-milk ratios. Our results suggest that soils and forages around farms near industries, as well as the milk produced from those farms, have generally low levels of PTE and PAH contaminants.

Characterization, risk assessment, and source estimation of PM10-bound polycyclic aromatic hydrocarbons during wintertime in the ambient air of Basrah City, Iraq

In this study, the concentration and structure of polycyclic aromatic hydrocarbons (PAHs) associated with the ambient PM10 in Basrah City, Iraq have been investigated for the first time. From December 2021 to February 2022, PM10 samples were collected on quartz fiber filters, extracted using an optimized extraction protocol, and analyzed for the sixteen US EPA priority PAHs. The results indicated that 4- and 5-ring PAHs represent 52% of the total detected PAHs. The most abundant PAHs over the study period were chrysene (1.2 ± 1.5 ng m−3), fluorene (0.9 ± 1.4 ng m−3), and benzo[b]fluoranthene (0.7 ± 0.9 ng m−3). Source identification suggested that PM10-bound PAHs primarily originated from pyrogenic and petrogenic activities in Basrah City. In addition, the cancer risk associated to PAH exposure was assessed based on benzo[a]pyrene equivalent concentration and was found ranging from 0.07 to 6.32 ng m-3; hence, it exceeded the threshold limit of 1.0 ng m−3 established by the European legislation (EU, 2014). Benzo[a]pyrene was determined to be main contributor to total carcinogenic power of the detected PAHs, accounting for 50.3%, followed by dibenz[a,h]anthracene (22.3%). Similarly, benzo[a]pyrene represented a major contributor to PAH associated mutagenicity, accounting for 43.5% of the total.

Global Meta-analysis of Urine Microbiome: Colonization of Polycyclic Aromatic Hydrocarbon–degrading Bacteria Among Bladder Cancer Patients

BackgroundThe application of next-generation sequencing techniques has enabled characterization of urinary tract microbiome. Although many studies have demonstrated associations between the human microbiome and bladder cancer (BC), these have not always reported consistent results, thereby necessitating cross-study comparisons. Thus, the fundamental questions remain how we can utilize this knowledge. ObjectiveThe aim of our study was to examine the disease-associated changes in urine microbiome communities globally utilizing a machine learning algorithm. Design, setting, and participantsRaw FASTQ files were downloaded for the three published studies in urinary microbiome in BC patients, in addition to our own prospectively collected cohort. Outcome measurements and statistical analysisDemultiplexing and classification were performed using the QIIME 2020.8 platform. De novo operational taxonomic units were clustered using the uCLUST algorithm and defined by 97% sequence similarity and classified at the phylum level against the Silva RNA sequence database. The metadata available from the three studies included were used to evaluate the differential abundance between BC patients and controls via a random-effect meta-analysis using the metagen R function. A machine learning analysis was performed using the SIAMCAT R package. Results and limitationsOur study includes 129 BC urine and 60 healthy control samples across four different countries. We identified a total of 97/548 genera to be differentially abundant in the BC urine microbiome compared with that of healthy patients. Overall, while the differences in diversity metrics were clustered around the country of origin (Kruskal-Wallis, p < 0.001), collection methodology was a driver of microbiome composition. When assessing dataset from China, Hungary, and Croatia, data demonstrated no discrimination capacity to distinguish between BC patients and healthy adults (area under the curve [AUC] 0.577). However, inclusion of samples with catheterized urine improved the diagnostic accuracy of prediction for BC to AUC 0.995, with precision-recall AUC = 0.994. Through elimination of contaminants associated with the collection methodology among all cohorts, our study identified increased abundance of polycyclic aromatic hydrocarbon (PAH)-degrading bacteria Sphingomonas, Acinetobacter, Micrococcus, Pseudomonas, and Ralstonia to be consistently present in BC patients. ConclusionsThe microbiota of the BC population may be a reflection of PAH exposure from smoking, environmental pollutants, and ingestion. Presence of PAHs in the urine of BC patients may allow for a unique metabolic niche and provide necessary metabolic resources where other bacteria are not able to flourish. Furthermore, we found that while compositional differences are associated with geography more than with disease, many are driven by the collection methodology. Patient summaryThe goal of our study was to compare the urine microbiome of bladder cancer patients with that of healthy controls and evaluate any potential bacteria that may be more likely to be found in patients with bladder cancer. Our study is unique as it evaluates this across multiple countries, to find a common pattern. After we removed some of the contamination, we were able to localize several key bacteria that are more likely to be found in the urine of bladder cancer patients. These bacteria all share their ability to break down tobacco carcinogens.

Polycyclic aromatic hydrocarbons (PAHs) and soot formations under different gasifying agents: Detailed chemical kinetic analysis of a two-stage entrained flow coal gasifier

The injection of CO2 with coal into coal gasifier is a promising approach to achieve CO2 recirculation. Predicting the formation and evolution of polycyclic aromatic hydrocarbons (PAHs) and soot during coal gasification is particularly important as their presence poses challenges to the gasifier operation and environment. However, the effect of CO2 injection on their formation must be elucidated in more detail to optimize the gasifier design. This work investigates PAHs and soot formations in gas-phase reactions under different gasifying agents (Air, O2/CO2, O2/H2O) in a two-stage entrained flow coal gasifier using a detailed chemical kinetic model (DCKM). Under the O2/CO2– and O2/H2O-blown conditions, aromatics reforming was progressed whereas the yields of tar and soot were effectively suppressed. The benzene was observed as the most abundant PAHs species, followed by naphthalene and acenaphthalene. Regarding the relative oxygen concentration, the conversion behavior of aromatics was significantly influenced in the O2/CO2-blown condition, while the somewhat effect was found in the O2/H2O-blown condition. Tar yield peaked at 50% relative oxygen concentration in the O2/CO2-blown condition. The present finding may have practical significance in the O2/CO2-blown gasifier to facilitate CO2 recirculation for the oxy-fuel IGCC system.

Deposition of atmospheric polycyclic aromatic hydrocarbons in rural areas: Current data and historical record from an ombrotrophic peatland

Atmospheric concentrations of 18 polycyclic aromatic hydrocarbons (PAHs) were measured in a rural area in northern Spain. Both the gas phase and particulate fraction were determined to evaluate the types and abundance of PAHs taken up by vegetation and the historical record of PAH deposition in an ombrotrophic peatland over the last 300 years. The total atmospheric PAH concentration was ca. 2.5 ng m−3, a value that is slightly lower value than those found in other rural areas, consistent with those of remote areas (Pyrenees, Alps, and Caledonian Mountains), and much lower than those recorded in urban areas. The particulate fraction showed a greater content of high molecular weight PAHs, whereas the gas phase was enriched in low molecular weight homologues. The concentration of total PAHs in the gas phase was higher than that in the particulate fraction (ca. 80%) and similar to that found in other localities in remote areas. PAHs showed seasonal variability. In this regard, the highest concentrations in the gas phase occurred in winter and autumn, whereas in the particulate fraction they were found in winter and spring. Of note, the concentrations of PAHs increased in the particulate fraction during the years in which fires occurred. The PAH content in peat-forming plants in this area showed a similar distribution to that of the gas phase. The historical record of the depositional fluxes of PAHs in an ombrotrophic peatland in the study area, which was dated radiometrically, allowed to reconstruct the changes in pollutant content between 1775 and the present. In general, the PAHs detected were of pyrogenic origin (fossil fuels and wood combustion). The concentrations of these pollutants increased from uniform background levels at the turn of the second half of the 19th century, which were linked to industrial development, to maximum values during the first half of the 20th century until the beginning of the 21st century, when the extraction and combustion of coal was extensive close to the study area. In contrast, in the uppermost part of the record, PAH concentrations decreased. This reduction is attributed to the implementation of environmental policies, although the concentrations of these pollutants were still greater than during the preindustrial period. To gain a detailed understanding of the deposition and evolution of PAHs in the study area, here it is reported on a new method that integrates current atmospheric data on PAHs with information on their accumulation in plants and the historical peat record of a rural area in Spain. The methodology described herein could be applied to other scenarios in the context of PAH pollution.

Using fly larvae to convert food waste for growing Oujiang color common carps: health risk assessment of polycyclic aromatic hydrocarbons.

The present study used Chrysomya megacephala larvae (CML) to transform food waste into safe and high-quality fish feed to substitute fish meal as a source of protein for growing Oujiang color common carps followed by a human health risk assessment of polycyclic aromatic hydrocarbons (PAHs). The results showed the ∑PAH concentration in the CML fed with food waste ranged from 50 to 370μgkg-1, and the most abundant PAH compound in the CML was BaP, contributing 59-84% of ∑PAHs. The Pearson correlation analysis results indicated no correlation between the ∑PAH concentrations and the culture substrate ratio (p > 0.05). Concentrations of BaP in the CML decreased with the increase of breeding density (p < 0.01). The residues as organic fertilizers have no potential ecological risk for PAHs. The biotransformed larva meal was used to partially or completely replace the fish meal as supplementary protein in the experimental feeds (T0, 0%; T50, 50%; T100, 100%). No significant difference (p < 0.05) of survival rate, lipid, and protein content in Oujiang color common carp was noted among T0, T50, and T100 fish feeds. Concentrations of ∑PAHs in Oujiang color common carp fed with the CML fish feeds all met the food safety standards in the European Union (EU). Furthermore, the consumption of Oujiang color common carps fed with the CML feed does not pose any health risks of PAHs for humans.

Gas Particle Partitioning of PAHs Emissions from Typical Solid Fuel Combustions as Well as Their Health Risk Assessment in Rural Guanzhong Plain, China.

Air pollutants from the incomplete combustion of rural solid fuels are seriously harmful to both air quality and human health. To quantify the health effects of different fuel-stove combinations, gas and particle partitioning of twenty-nine species of polycyclic aromatic hydrocarbons (PAHs) emitted from seven fuel-stove combinations were examined in this study, and the benzo (a) pyrene toxicity equivalent (BaPeq) and cancer risks were estimated accordingly. The results showed that the gas phase PAHs (accounting for 68-78% of the total PAHs) had higher emission factors (EFs) than particulate ones. For all combustion combinations, pPAHs accounted for the highest proportion (84.5% to 99.3%) in both the gas and particulate phases, followed by aPAHs (0.63-14.7%), while the proportions of nPAHs and oPAHs were much lower (2-4 orders of magnitude) than pPAHs. For BaPeq, particulate phase PAHs dominated the BaPeq rather than gas ones, which may be due to the greater abundance of 5-ring particle PAHs. Gas and particle pPAHs were both predominant in the BaPeq, with proportions of 95.2-98.6% for all combustion combinations. Cancer risk results showed a descending order of bituminous coal combustion (0.003-0.05), biomass burning (0.002-0.01), and clean briquette coal combustion (10-5-0.001), indicating that local residents caused a severe health threat by solid fuel combustion (the threshold: 10-4). The results also highlighted that clean briquette coal could reduce cancer risks by 1-2 orders of magnitude compared to bulk coal and biomass. For oPAH, BcdPQ (6H-benzo(c,d)pyrene-6-one) had the highest cancer risk, ranging from 4.83 × 10-5 to 2.45 × 10-4, which were even higher than the total of aPAHs and nPAHs. The dramatically high toxicity and cancer risk of PAHs from solid fuel combustion strengthened the necessity and urgency of clean heating innovation in Guanzhong Plain and in similar places.

The amino acid and polycyclic aromatic hydrocarbon compositions of the promptly recovered CM2 Winchcombe carbonaceous chondrite

AbstractThe rapid recovery of the Winchcombe meteorite offers a valuable opportunity to study the soluble organic matter (SOM) profile in pristine carbonaceous astromaterials. Our interests in the biologically relevant molecules, amino acids—monomers of protein, and the most prevalent meteoritic organics—polycyclic aromatic hydrocarbons (PAHs) are addressed by analyzing the solvent extracts of a Winchcombe meteorite stone using gas chromatography mass spectrometry. The Winchcombe sample contains an amino acid abundance of ~1132 parts‐per‐billion that is about 10 times lower than other CM2 meteorites. The detection of terrestrially rare amino acids, including α‐aminoisobutyric acid (AIB); isovaline; β‐alanine; α‐, β‐, and γ‐amino‐n‐butyric acids; and 5‐aminopentanoic acid, and the racemic enantiomeric ratios (D/L = 1) observed for alanine and isovaline indicate that these amino acids are indigenous to the meteorite and not terrestrial contaminants. The presence of predominantly α‐AIB and isovaline is consistent with their formation via the Strecker‐cyanohydrin synthetic pathway. The L‐enantiomeric excesses in isovaline previously observed for aqueously altered meteorites were viewed as an indicator of parent body aqueous processing; thus, the racemic ratio of isovaline observed for Winchcombe, alongside the overall high free:total amino acid ratio, and the low amino acid concentration suggest that the analyzed stone is derived from a lithology that has experienced brief episode(s) of aqueous alteration. Winchcombe also contains 2‐ to 6‐ring alkylated and nonalkylated PAHs. The low total PAHs abundance (6177 ppb) and high nonalkylated:alkylated ratio are distinct from that observed for heavily aqueously altered CMs. The weak petrographic properties of Winchcombe, as well as the discrepancies observed for the Winchcombe SOM content—a low total amino acid abundance comparable to heavily altered CMs, and yet the high free:total amino acid and nonalkylated:alkylated PAH ratios are on par with the less altered CMs—suggest that Winchcombe could represent a class of weak, poorly lithified meteorite not been previously studied.

Sex-specific thyroid disruption caused by phenanthrene in adult zebrafish (Danio rerio)

Polycyclic aromatic hydrocarbons (PAHs) are well-known contaminants with widespread distribution in environment and food. Phenanthrene is one of the most abundant PAHs in food and aquatic environment and generates reproductive and developmental toxicity in zebrafish. Nonetheless, whether phenanthrene caused sex-specific thyroid disruption in adult zebrafish is unclear. To determine this, adult zebrafish (male and female) were treated with phenanthrene (0, 0.85, 8.5, and 85 μg/L) for 60 days. After the treatment period, we assessed the concentrations of thyroid hormones (THs) and expression levels of genes in the hypothalamic-pituitary-thyroid (HPT) axis. The results showed that phenanthrene exposure can lead to thyroid disruption in both male and female zebrafish. Exposure to phenanthrene dramatically reduced the levels of L-thyroxine (T4) and L-triiodothyronine (T3) in both male and female zebrafish, with a similar trend in both. However, the genes expression profiles of hypothalamic-pituitary-thyroid (HPT) axis were sex-specific. In all, the present study demonstrated that phenanthrene exposure could result in sex-specific thyroid disruption in adult zebrafish.

Exposure to phenanthrene affects oocyte meiosis by inducing mitochondrial dysfunction and endoplasmic reticulum stress.

Phenanthrene (PHE) is one of the most abundant polycyclic aromatic hydrocarbons (PAHs), which is a widespread environmental contaminant. Various studies showed that PHE has adverse impacts on animals and human health. It has been shown that PHE exposure induced follicular atresia and endocrine dyscrasia in female mice. However, the potential mechanism regarding how PHE affects female reproductive system especially the oocyte quality has not been elucidated. In this study, we set up PHE exposure model and found that PHE exposure compromised oocytes maturation competence by inhibiting spindle assembly and chromosomes alignment. Moreover, PHE exposure induced mitochondrial dysfunction and endoplasmic reticulum (ER) stress, leading to increased reactive oxygen species (ROS) and aberrant calcium levels in cytoplasm, eventually induced oxidative stress and DNA damage in oocytes. Furthermore, we found that oral administration of PHE caused the occurrence of oxidative stress and apoptosis in female ovary. In addition, the oocyte exhibited aberrant spindle morphology and failure of actin cap formation in metaphase II oocytes. Taken together, our study demonstrated that mitochondrial dysfunction and ER stress-induced oxidative stress and DNA damage are the major cause of poor oocyte quality after PHE exposure.

Optimized LC-MS/MS method for simultaneous determination of endocrine disruptors and PAHs bound to PM2.5: Sources and health risk in Indo-Gangetic Plain

Airborne particulate matter (PM) is a serious health threat when it is bound to hazardous pollutants like phthalic acid esters (PAEs) (endocrine disruptors) and polycyclic aromatic hydrocarbons (PAHs). In this study, an optimized method was developed and validated for the simultaneous screening and quantification of PAEs (dimethyl phthalate (DMP), diethyl phthalate (DEP), benzyl butyl phthalate (BBP), dibutyl phthalate (DBP), bis (2-ethyl hexyl) phthalate (DEHP), bis(2-ethylhexyl) adipate (DEHA), di-n-octyl phthalate (DNOP)) and PAHs (benzo[a]anthracene (B[a]A), benzo[b]fluorenthene (B[b]F), benzo[k]fluorenthene (B[k]F), benzo[a]pyrene (B[a]P), dibenzo[ah]anthracene (D[ah]A), benzo[ghi]perylene (B[ghi]P), and indeno[1,2,3-cd]pyrene (IND)) bound to ambient PM2.5 using liquid chromatography coupled to electrospray ionization tandem mass spectrometer (LC-ESI-MS/MS). The developed method exhibited excellent linearity (r2 > 0.99), precision error less than 10%, good recovery percentages (90%–120%, except for DMP ≈ 65%). After the validation, this method was deployed to investigate the seasonal variation and source identification of targeted compounds bound to ambient PM2.5 at a measurement site in the North West Indo-Gangetic Plain (NWIGP). In this study, the most abundant PAE and PAH are DEHP (17.94 ng m−3) and B[b]F (36.13 ng m−3), respectively. Measured concentrations of B[a]P, Group 1 carcinogen (4.66 ng m−3) had exceeded the National Ambient Air Quality Standards, India (1 ng m−3). Diagnostic ratios (DRs) revealed that fossil fuel/diesel combustions are the major emission sources of PAHs in summer and monsoon while biomass/coal combustions in winter season at the sampling site. Further, incremental lifetime cancer risk (ILCR) for adults and children due to exposure to PM2.5 bound DEHP (adults: 0.3678 × 10−6 and children: 0.8792 × 10−6) and B[a]Peq (adults: 1.40 × 10−5 and children: 3.272 × 10−5) were estimated. Estimated ILCR values for B[a]Peq exceeded the threshold value (1 × 10−6) set by USEPA. Findings in this study reveal that the health risk due to exposure to PAEs and PAHs bound to PM2.5 should be of concern.

Histology study and transcriptome analysis of the testis of Loach(Misgurnus anguillicaudatus) in response to phenanthrene exposure

Phenanthrene (PHE) is one of the most abundant polycyclic aromatic hydrocarbon compounds (PAHs) in the aquatic environment. The loaches were exposed at concentrations of 0.30、1.00、3.00 mg L−1 for 60 days. The effects of PHE on the testis development were evaluated by calculating the survival rate, observing the structure of testis and analyzing transcriptome. Firstly, PHE markedly decreased the survival rate in a dose-dependent manner. Then, the number and density of spermatogonia, primary spermatocytes, secondary spermatocytes and spermatids were substantially reduced under PHE exposure. The space in the seminiferous tubule obviously increased in the high PHE concentration group. Meanwhile, transcriptome comparative analysis identified 5329 differentially expressed genes (DEGs) including 2928 up-regulated and 2401 down-regulated in the testis of loach exposed PHE for 60 days. Meiotic cell cycle, arganelle fission, ATPase activity and adenylate nucleotide binding were significantly differences by GO (Gene Ontology) enrichment. KEGG (Kyoto Encyclopedia of Genes and Genomes) pathway analysis revealed that TNF (Tumor Necrosis Factor) signaling pathway, CAMs (Cell Adhesion Molecules), cytochrome P450 and lipid metabolism were markedly regulated. In addition, eight DEGs were randomly selected from the testis transcriptomics results for qPCR verification, the results were consistent with RNA-Seq. Finally, related genes (piwil2, dmc1, vasa, ubr2, dnd, rnf17, plcb2, c-fos, gpx4) of testis development were further confirmed and they were differentially regulated after PHE exposure. In summary, a survey of the mechanism of loach testis response to PHE was performed, and a large number of gene expression levels regarding metabolism, spermatogenesis and immunity genes were acquired from RNA-seq. This study provide informations for elucidating the molecular mechanism of PHE affected the testis development of loach.

Competitive Metabolism of Polycyclic Aromatic Hydrocarbons (PAHs): An Assessment Using In Vitro Metabolism and Physiologically Based Pharmacokinetic (PBPK) Modeling.

Humans are routinely exposed to complex mixtures such as polycyclic aromatic hydrocarbons (PAHs) rather than to single compounds, as are often assessed for hazards. Cytochrome P450 enzymes (CYPs) metabolize PAHs, and multiple PAHs found in mixtures can compete as substrates for individual CYPs (e.g., CYP1A1, CYP1B1, etc.). The objective of this study was to assess competitive inhibition of metabolism of PAH mixtures in humans and evaluate a key assumption of the Relative Potency Factor approach that common human exposures will not cause interactions among mixture components. To test this objective, we co-incubated binary mixtures of benzo[a]pyrene (BaP) and dibenzo[def,p]chrysene (DBC) in human hepatic microsomes and measured rates of enzymatic BaP and DBC disappearance. We observed competitive inhibition of BaP and DBC metabolism and measured inhibition coefficients (Ki), observing that BaP inhibited DBC metabolism more potently than DBC inhibited BaP metabolism (0.061 vs. 0.44 µM Ki, respectively). We developed a physiologically based pharmacokinetic (PBPK) interaction model by integrating PBPK models of DBC and BaP and incorporating measured metabolism inhibition coefficients. The PBPK model predicts significant increases in BaP and DBC concentrations in blood AUCs following high oral doses of PAHs (≥100 mg), five orders of magnitude higher than typical human exposures. We also measured inhibition coefficients of Supermix-10, a mixture of the most abundant PAHs measured at the Portland Harbor Superfund Site, on BaP and DBC metabolism. We observed similar potencies of inhibition coefficients of Supermix-10 compared to BaP and DBC. Overall, results of this study demonstrate that these PAHs compete for the same enzymes and, at high doses, inhibit metabolism and alter internal dosimetry of exposed PAHs. This approach predicts that BaP and DBC exposures required to observe metabolic interaction are much higher than typical human exposures, consistent with assumptions used when applying the Relative Potency Factor approach for PAH mixture risk assessment.

Gas temperature structure across transition disk cavities

Context. Most disks observed at high angular resolution show signs of substructures, such as rings, gaps, arcs, and cavities, in both the gas and the dust. To understand the physical mechanisms responsible for these structures, knowledge about the gas surface density is essential. This, in turn, requires information on the gas temperature. Aims. The aim of this work is to constrain the gas temperature as well as the gas surface densities inside and outside the millimeter-dust cavities of two transition disks: LkCa15 and HD 169142, which have dust cavities of 68 AU and 25 AU, respectively. Methods. We use some of the few existing ALMA observations of the J = 6-5 transition of 13CO together with archival J = 2−1 data of 12CO, 13CO, and C18O. The ratio of the 13CO J = 6−5 to the J = 2−1 transition is used to constrain the temperature and is compared with that found from peak brightness temperatures of optically thick lines. The spectra are used to resolve the innermost disk regions to a spatial resolution better than that of the beam of the observations. Furthermore, we use the thermochemical code DALI to model the temperature and density structure of a typical transition disk as well as the emitting regions of the CO isotopologs. Results. The 13CO J = 6−5 and J = 2−1 transitions peak inside the dust cavity in both disks, indicating that gas is present in the dust cavities. The kinematically derived radial profiles show that the gas is detected down to 10 and 5-10 AU, much farther in than the dust cavities in the LkCa15 and HD 169142 disks, respectively. For LkCa15, the steep increase toward the star in the 13CO J = 6−5 transition, in contrast to the J = 2−1 line, shows that the gas is too warm to be traced by the J = 2−1 line and that molecular excitation is important for analyzing the line emission. Quantitatively, the 6−5/2−1 line ratio constrains the gas temperature in the emitting layers inside the dust cavity to be up to 65 K, warmer than in the outer disk, which is at 20-30 K. For HD 169142, the lines are optically thick, complicating a line ratio analysis. In this case, the peak brightness temperature constrains the gas in the dust cavity of HD 169142 to be 170 K, whereas that in the outer disk is only 100 K. The data indicate a vertical structure in which the 13CO 6-5 line emits from a higher layer than the 2-1 line in both disks, consistent with exploratory thermochemical DALI models. Such models also show that a more luminous central star, a lower abundance of polycyclic aromatic hydrocarbons, and the absence of a dusty inner disk increase the temperature of the emitting layers and hence the line ratio in the gas cavity. The gas column density in the LkCa15 dust cavity drops by a factor of &gt;2 compared to the outer disk, with an additional drop of an order of magnitude inside the gas cavity at 10 AU. In the case of HD 169142, the gas column density drops by a factor of 200–500 inside the gas cavity. Conclusions. The gas temperatures inside the dust cavities steeply increase toward the star and reach temperatures of up to 65 K (LkCa15) and 170 K (HD 169142) on scales of ~15–30 AU, whereas the temperature gradients of the emitting layers in the outer disks are shallow, with typical temperatures of 20-30 and 100 K, respectively. The deep drop in gas column density inside the HD 169142 gas cavity at &lt;10 AU could be due to a massive companion of several MJ, whereas the broad dust-depleted gas region from 10 to 68 AU for LkCa15 may imply several lower mass planets. This work demonstrates that knowledge of the gas temperature is important for determining the gas surface density and thus whether planets, and if so what kinds of planets, are most likely to be carving the dust cavities.

Rapid Screening of 22 Polycyclic Aromatic Hydrocarbons Residues in Vegetable Oils by Gas Chromatography-Electrostatic Field Orbitrap High Resolution Mass Spectrometry.

A method for simultaneous determination of 22 polycyclic aromatic hydrocarbons (PAHs) residues in vegetable oils by gas chromatography-electrostatic field orbitrap high resolution mass spectrometry (Orbitrap GC-MS) was established. The samples were vortexed with acetonitrile, centrifuged at 8,000 r/min for 5 min, and frozen at −70°C for 10 min. The extracts of upper layer were poured out, dried with nitrogen at 40°C, redissolved in dichloromethane, and measured by Orbitrap GC-MS. The matrix interference in vegetable oil could be effectively removed by determining the accurate mass number of target compounds under the full scan mode. Six typical vegetable oil samples (soybean oil, sesame oil, peanut oil, olive oil, rapeseed oil, sunflower oil) were used for method validation. The calibration curve displayed good linearity in the range of 1–100 ng/mL, with correlation coefficients > 0.9950. The limits of detection (LODs) were in the range of 0.10–0.60 μg/kg, and the limits of quantification (LOQs) were in the range of 0.35–2.00 μg/kg. The average spiked recoveries of 22 PAHs in 6 matrices at 5, 50 and 100 μg/kg levels were 76.4–115.4%, and the average relative standard deviations (RSDs) were 1.8–10.8%. The results showed that 22 PAHs were detected in 6 types of 90 edible vegetable oil samples in the Chinese market by this method. Meanwhile, the abundance of light PAHs (LPAHs) was higher than that of heavy PAHs (HPAHs), and its relative contribution of LPAHs to the total PAHs was higher. All levels of BaP conformed to the Chinese requirement of upper limit, 10 μg/kg. However, 13.3 and 11.1% of the samples exceeded the maximum limits of BaP and PAH4 set by EU, 2 and 10 μg/kg, respectively. The total concentrations of 22 PAHs (defined as PAH22) varies greatly among different oil species, and the average PAH22 contents were listed in descending order as follows: peanut oil > sesame oil > olive oil > rapeseed oil > soybean oil > sunflower seed oil. The established method effectively avoided interference from large amounts of lipids and pigments. Therefore, the method is simple, sensitive and suitable for rapid screening and confirmation of PAHs in vegetable oil.

Cu, Co embedded N-enriched mesoporous carbon cathode catalyst for the efficient bioelectrochemical removal of phenanthrene in microbial fuel cell

The development of high-efficiency and economical oxygen reduction reaction (ORR) electrocatalysts is vital for the improvement of renewable energy storage and conversion technology. As a promising energy conversion technology, the performance of microbial fuel cell (MFC) has aroused worldwide interest in recent years owing to its power generation capacity and potential for wastewater treatment. In an aquatic environment, phenanthrene (Phe) is one of the most abundant polycyclic aromatic hydrocarbons. We synthesized a series of CuCo samples successfully via simple in- situ growth and thermal decomposition method. In addition, a single-chamber, air-cathode MFC is investigated for the degradation of phenanthrene in neutral solution. The cathode catalyst 1.5 CuCo@NC-800 exhibits a maximum power density (MPD) of 3248.68 ± 28.21 mW m−2 in initial cycles and maintained at 95.25% after the Phe degradation. And in this study, the reactor with 1.5 CuCo@NC-800 catalyst can effectively reduce Phe at low concentrations and remain above the rate of 98%. Therefore, 1.5 CuCo@NC-800 showed great potential to become a material candidate for non-noble cathode catalyst in MFC.

Detecting PAHs in high-z galaxies in proxy: modelling physical conditions in an extremely strong damped Lyman α absorber towards QSO SDSS J1143+1420 at z = 2.323

ABSTRACT We explore indirect methods to detect polycyclic aromatic hydrocarbons (PAHs) in gas-rich, absorption-selected galaxies at high redshift. We look at the optical X-Shooter observations of an intervening, extremely strong damped Lyman α absorber (or ESDLA, with log [N(H i) ≳ 21.7)] towards QSO SDSS J1143+1420 at redshift, zESDLA = 2.323. Literature studies have shown that this ESDLA contains signatures of dust and diffuse molecular hydrogen and it was specifically chosen for our study due to its close spatial proximity (impact parameter, $\rm \rho = 0.6\, \pm \, 0.3$kpc) with its associated galaxy. There is no direct detection of PAHs emission in the limited observations of infrared spectra along this sightline. Hence, we use cloudy numerical simulation modelling to indirectly probe the presence of PAHs in the ESDLA. We note that PAHs need to be included in the models to reproduce the observed column densities of warm H2 and C i. Thus, we infer the presence of PAHs indirectly in our ESDLA, with an abundance of PAH/H = 10−7.046. We also measure a low 2175 Å bump strength (E$\rm _{bump}\, \sim$0.03–0.19 mag) relative to star-forming galaxies by modelling extinction of quasar QSO spectra by dust at the absorber rest frame. This is consistent with the low PAH abundance obtained indirectly using cloudy modelling. Our study highlights the usage of cloudy modelling to indirectly detect PAH in high-redshift gas-rich absorption-selected galaxies.