Abundant Polycyclic Aromatic Hydrocarbons Research Articles

Electrochemical performance and response of bacterial community during phenanthrene degradation in single-chamber air-cathode microbial fuel cells.

Polycyclic aromatic hydrocarbons have attracted considerable attention for their carcinogenic, teratogenic, and mutagenic properties in humans. Phenanthrene is one of the most abundant polycyclic aromatic hydrocarbons in aquatic environments. In this study, different concentrations of phenanthrene were degraded by single-chamber air-cathode microbial fuel cells. The electrochemical parameter of microbial fuel cells and biofilm changes on the anode were observed. The results showed that the addition of phenanthrene reduced the power output of the microbial fuel cell which affected the process of microbial electricity generation. Meanwhile, microorganisms destroyed the original structure of phenanthrene through anaerobic metabolism, and achieved good average degradation of 94.9-98.4%. Observation of the anodic biofilm found that the microbes had tolerance to phenanthrene and the biofilm exhibited to be well-constructed. Bacterial community distribution showed a decrease in the relative abundance of Acidovorax and Aquamicrobium, whereas the relative content of the main electroactive organism, Geobacter, increased by a factor of three. The results show that it is feasible for microbial fuel cells to biodegrade phenanthrene, and provide some references for the changes of microbial community during degradation process.

Estimating temporal and spatial levels of PAHs in air using rain samples and SPME analysis: Feasibility evaluation in an urban scenario

There is a growing interest in evaluating the role of concentration changes of contaminants in temporal and spatial gradients. This is often relevant for fast moving environmental phases such as air and water. In this paper, small volumes of rainwater were sampled as proxy for air concentrations of Polycyclic Aromatic Hydrocarbons (PAHs): rain was collected in three sampling sites (high traffic, restricted traffic and a low traffic zone) in Como. Solid phase micro extraction (SPME) was used for the extraction to reduce required sample volumes, allowing the acquisition of more samples in time. Rain samples highlighted a spatial and temporal variability along a traffic gradient in the Como city, especially for the most abundant PAH, e.g. phenanthrene. Air concentrations were then estimated from rain concentrations. The results show that this is a cheap and promising method, although requiring rainfall/snowfall conditions, that can be used to perform monitoring campaign of air concentrations at a higher temporal and spatial resolution than the adopted standard methods (e.g. high-volume air samplers). The results could be employed for evaluation of the exposure, emission profiles and calibration of fate models.

In-Cylinder Polycyclic Aromatic Hydrocarbons Sampled during Diesel Engine Combustion.

Polycyclic aromatic hydrocarbons (PAHs) are potentially carcinogenic pollutants emitted by diesel engines, both in the gas phase and adsorbed onto the surface of particulate matter (PM). There remains limited understanding of the complex and dynamic competing mechanisms of PAH formation, growth and oxidation in the gas phase, and their adsorption onto soot and how these processes impact on the abundance and composition of exhaust PAH. Therefore, this paper presents analysis of gas and particulate samples taken from the cylinder and exhaust of a diesel engine during combustion of fossil diesel with the 16 US-EPA priority PAH species identified and quantified. In-cylinder results showed that gas-phase PAHs were more abundant than soot-bound PAHs in the engine cylinder. The in-cylinder PAHs included 2- to 6-ring PAHs; however, 6-ring PAHs were not observed in the soot samples collected from the engine exhaust. Levels of both PM and the total in-cylinder PAHs decreased following a peak at 10 CAD ATDC but subsequently increased significantly during the late combustion phase. The B[a]P equivalence of PM in the engine cylinder increased during the period of early diffusion to late combustion phase, following an initial decrease during the period of premixed to early diffusion combustion.

Bioremediation of petroleum-contaminated soil by semi-aerobic aged refuse biofilter: Optimization and mechanism

Petroleum-contaminated soil (PCS) is a global environmental issue. An effective remediation technique is urgently needed to address this problem. This study applied a semi-aerobic aged refuse biofilter (SAARB) to the decontamination and remediation of PCS. The effects of petroleum content, surfactant content, and water content on oil removal efficiency were studied, and the operation conditions were optimized using the response surface method. Results showed that contents of petroleum and water that were too high or too low depressed total petroleum hydrocarbon (TPH) removal. The presence of surfactant markedly reduced the TPH removal efficiency. The optimal operation conditions were the ratio of aged refuse to PCS = 1.6; water content = 41%; and petroleum content = 3.8%. The TPH removal efficiencies under optimized conditions and during a confirmatory experiment were 59.89% and 51.38%, respectively. PCS contained an abundance of polycyclic aromatic hydrocarbons and macro molecular alkanes, and these organic compounds were considerably removed by SAARB treatment. The microbial community exhibited a marked change at both phylum level and genus level after 3 months of remediation in the PCS. At the genus level, norank_f_SS1–B-06-26 became the most dominant; further isolation and verification experiments for its ability to degrade petroleum are needed. In addition, the abundance of norank_o_Saccharimonadales, Aquabacterium, Hydrogenophaga, and norank_f_Saccharimonadaceae, which can degrade hydrocarbons, also increased. This study provides a theoretical reference for SAARB application in the remediation of PCS.

Coordinated effects of air pollution control devices on PAH emissions in coal-fired power plants and industrial boilers

Coal-fired power plants are important sources of polycyclic aromatic hydrocarbon (PAH) emissions in the world. The effects of various air pollution control devices (APCDs) on PAH emissions were investigated by analyzing samples from inlets and outlets of APCDs in six coal-fired power plants (A–F) and two coal-fired industrial boilers (G and H). The APCDs were electrostatic precipitators (ESPs), wet flue gas desulfurization systems (WFGDs), and wet ESPs (WESPs). The PAH congener patterns for the coal-fired plants were similar. Gas-phase PAHs were dominant in flue gases, and the most abundant PAH was naphthalene. Three- and four-ring PAHs were dominant in fly ash. Positive correlations were found between the PAH and total organic carbon contents of fly ash (R2 0.87) and slag (R2 0.92). Plants D–F, equipped with low-low-temperature ESPs (LLT-ESPs) and WESPs discharged the lowest PAHs. Circulating water was an important source of PAHs in the desulfurization except in plant A, which used desalinated seawater rather than circulating water in the desulfurization process. WESPs decreased PAH concentrations by an average of 20.67%, which can be spread to other plants to reduce PAHs.

Effect of temperature on Shenfu coal pyrolysis process related to its chemical structure transformation

Revealing the pyrolysis reaction pathway related to coal structure evolution under different temperatures is important for the industry to design reactors and process operations. In this study, all the pyrolysis products obtained under different pyrolysis temperatures were comprehensively analyzed by multiple techniques. The results showed that the aromatic nucleus were inclined to react with methyl radicals, forming char with abundant methyl substitution aromatic structure at low pyrolysis temperature. At medium pyrolysis temperature, dramatically condensation reaction occurred, resulting in the formation of aromatic protonated carbon and abundant polycyclic aromatic hydrocarbons (PAHs) containing benzenoid rings joined by a carbon‑carbon single bond remaining in char. The concentration of aliphatic hydrocarbons in light tar decreased dramatically and converted into light hydrocarbon gas compounds (especially H2 and CH4). At high pyrolysis temperature, severe carbonation of char led to the formation of abundant PAHs with reduced aliphatic side chain in light tar. Tar precursors preferred to form larger PAHs due to occurrence of drastic secondary reaction. The contents and diversity of oxygen−/nitrogen-containing heteroatom compounds in heavy tar were significantly reduced with the increase of temperature. Finally, the devolatilization mechanism responsible for the evolution of chemical structure of Shenfu coal pyrolyzed at elevated temperatures was proposed.

Molecular content of nascent soot: Family characterization using two-step laser desorption laser ionization mass spectrometry

Molecules constituting nascent soot particles have been analyzed by two-step laser desorption laser ionization mass spectrometry. Three samples have been collected from a slightly sooting ethylene/air premixed flame with the aim to investigate soot composition in the transition from nucleated to just-grown soot particles. Sampling locations have been selected based on the evolution of the particle size distribution along the flame axis. The mass spectrometric results point to a strong evolution of the molecular composition. Just-nucleated soot is rich in polycyclic aromatic hydrocarbons (PAHs) dominated by medium sizes from 18 to 40 carbon atoms but containing sizes as large as 90 carbon atoms. Most abundant PAHs are in the form of peri-condensed structures. The presence of a large fraction of odd numbered carbon species shows that pentagonal cycles are a common feature of the detected population. Increasing the distance from the burner outlet, i.e., the particle residence time in flame, leads to an evolution of the chemical composition of this population with a major contribution of carbon clusters including also fullerenes up to about 160 carbon atoms. Our data support a scenario in which large PAHs containing pentagonal rings evolve very efficiently upon thermal processing by a series of dehydrogenation and isomerization processes to form fullerenes. This chemistry happens in the early steps of soot growth showing that carbonization is already active at this stage.

Inflammation response, oxidative stress and DNA damage caused by urban air pollution exposure increase in the lack of DNA repair XPC protein

Air pollution represents a considerable threat to health worldwide. The São Paulo Metropolitan area, in Brazil, has a unique composition of atmospheric pollutants with a population of nearly 20 million people and 9 million passenger cars. It is long known that exposure to particulate matter less than 2.5 µm (PM2.5) can cause various health effects such as DNA damage. One of the most versatile defense mechanisms against the accumulation of DNA damage is the nucleotide excision repair (NER), which includes XPC protein. However, the mechanisms by which NER protects against adverse health effects related to air pollution are largely unknown. We hypothesized that reduction of XPC activity may contribute to inflammation response, oxidative stress and DNA damage after PM2.5 exposure. To address these important questions, XPC knockout and wild type mice were exposed to PM2.5 using the Harvard Ambient Particle concentrator. Results from one-single exposure have shown a significant increase in the levels of anti-ICAM, IL-1β, and TNF-α in the polluted group when compared to the filtered air group. Continued chronic PM2.5 exposure increased levels of carbonylated proteins, especially in the lung of XPC mice, probably as a consequence of oxidative stress. As a response to DNA damage, XPC mice lungs exhibit increased γ-H2AX, followed by severe atypical hyperplasia. Emissions from vehicles are composed of hazardous substances, with polycyclic aromatic hydrocarbons (PAHs) and metals being most frequently cited as the major contributors to negative health impacts. This analysis showed that benzo[b]fluoranthene, 2-nitrofluorene and 9,10-anthraquinone were the most abundant PAHs and derivatives. Taken together, these findings demonstrate the participation of XPC protein, and NER pathway, in the protection of mice against the carcinogenic potential of air pollution. This implicates that DNA is damaged directly (forming adducts) or indirectly (Reactive Oxygen Species) by the various compounds detected in urban PM2.5.

Investigation and Assessment of Polycyclic Aromatic Hydrocarbons Concentrations in Sediments at Drainage Discharge Points into the Mangrove Stretch of New Calabar River, Port Harcourt, Nigeria

Sediment samples were collected from surface of sediments from parts of the mangrove wetlands of the New Calabar River at points of effluents discharge. The samples were treated according to standard procedures and analyzed for the concentrations of polycyclic aromatic hydrocarbons (PAHs). The results showed the presence of ten PAHs at Iwofe Jetty and Police Post stations and eleven PAHs at the Minipiti station. The summation of the total PAHs in the stations showed 23.440, 33.694 and 51.094 mg/Kg in sediments from Iwofe Jetty, Minipiti and Police Post stations respectively. Pyrene was the most abundant PAH in sediment from Iwofe station, Dibenzo (a,h) anthracene was the most abundant PAH at the Minipiti Station and acenaphthylene was the most abundant PAH at the Police Post Station. The categorization of the PAHs classes showed that the high molecular weight PAHs (HMW PAHS) were more abundant than the low molecular weight (PAHs) in all the stations examined, although, at the Police Post station, the values were very close. The 4-membered rings were more abundant in sediments from Iwofe Jetty station. The 4 and 5-membered rings were more abundant at the Minipiti station and the 2-3 membered rings were dominant at the police Post station. The 6-membered rings were the least abundant or undetected in all the stations. Source and origin diagnosis showed that LMW/ HMW PAHs as pyrogenic in all the stations, An/(An+Phe) ratio revealed pyrogenic sources of PAHs, Fl/(Fl+Pyr) analysis in all the stations indicated petrogenic origin of PAHs, BaA/ (BaA+Chr) evaluation in all the stations revealed pyrogenic sources of PAHs. The mixed sources of PAHs in the wetlands drainage discharge points calls for concern and therefore, efforts should be geared to identify the points at which they were introduced into the effluents and be adequately controlled to prevent harm to the environment.

Fire distinguishers: Refined interpretations of polycyclic aromatic hydrocarbons for paleo-applications

Polycyclic aromatic hydrocarbons (PAHs), produced via incomplete combustion of organics, convey signatures of vegetation burned in the geologic past. New and published burn experiments reveal how the quantity, distributions, and isotopic abundances of fire-derived PAHs were influenced by fuel types, burn conditions, and also phase. PAH concentrations were higher in burn residues from moderate burn temperatures (400–500 °C), and significantly lower in residues from cooler (<300 °C) or hotter (>600 °C) conditions, especially when oxygen was limited. PAH forms tended to be smaller in smoke samples and larger in residues, consistent with molecular physical and chemical properties. Plant functional types were distinguished by relative amounts of retene and dimethyl phenanthrene isomers. Isotopically distinct photosynthetic pathways of the burned material were reflected in the δ13C values of PAHs, which faithfully captured biomass signatures as well as the ∼12‰ offset between C3 and C4 plant types. PAH size, alkylation, and isotope characteristics can differentiate combusted plant types and distinguish between air-borne and sedimentary transport mechanisms. New proxy approaches using PAH amounts, distributions, and isotope signatures can aid and refine interpretations of paleofire ecology in the geologic record.

Both artificial root exudates and natural Koelreuteria paniculata exudates modify bacterial community structure and enhance phenanthrene biodegradation in contaminated soils

Polycyclic aromatic hydrocarbons (PAHs) are environmental pollutants that represent a serious threat to the health of humans and ecosystems. The effects of plant root and artificial root exudates (ARE) on the biodegradation of phenanthrene (PHE) and their impact on soil bacterial community structure was the focus of this work using four treatments for 180 days. Treatments included; control treatment (CK), low concentration of ARE (AREL), high concentration of ARE (AREH), and planting Koelreuteria paniculata saplings (KOE). The diversity and composition of soil bacterial community were analyzed using high-throughput sequencing. The results showed that KOE treatments had the most significant effect on the biodegradation of PHE compared to controls. ARE treatments had the similar effects on the biodegradation of PHE in soil with high efficiency in AREH than AREL. Both KOE and ARE treatments reduced diversity of bacterial community but increased the abundance of PAHs degrading bacterial populations within representative phyla, including Proteobacteria and Firmicutes. During the study, the total bacterial OTUs showed the number of unique genus types initially increased, then lowered in the later stages of the incubation process. Specific bacterial populations enriched by the treatments and supported by the exudates seemed to determine the biodegradation of PHE and not the overall bacterial diversity.

Extremely high abundance of polycyclic aromatic hydrocarbons in aerosols from a typical coal-combustion rural site in China: Size distribution, source identification and cancer risk assessment

Air quality in China is tending to improve, especially in urban areas. Nevertheless, rural areas and underdeveloped cities in northern China are still suffering from severe air pollution in winter due to large usage of coal and unfavorable meteorological conditions. In this study, size-segregated aerosol samples were collected from a typical coal-combustion rural site in Linfen, China during an extreme air pollution episode in winter 2017. The polycyclic aromatic hydrocarbons (PAHs), n-alkanes, hopanes and steranes were identified to better understand the emission sources of the organic compounds and the health effects of the PAHs in the ambient air here. The PAHs showed a bimodal mode with the major peak in the Aitken mode (<0.4 μm) and the minor one in the size range of 0.7–2.1 μm. Daily PAHs level ranged from 0.5–1.6 μg m−3 (average: 1.1 ± 0.3 μg m−3) which was 1–2 orders of magnitude higher than other major cities in China. The plots of log (PAH/PM)-log(Dp) showed the slope near −1 for four-, five- and six-ring PAHs, indicating both the adsorption and absorption mechanisms controlled the size distribution. The deposition efficiency displayed a bimodal mode in alveolar region (AR), and the major peak was within the Aitken mode. The total deposition flux (DF) in AR region was 92.7 ng h−1, and the DF based lifetime cancer risk (LCR) was about 2.7 × 10−4 for adults and 2.0 × 10−4 for children which were 2 orders of magnitude higher than the acceptable level of 10−6 proposed by United States Environmental Protection Agency (US EPA). In summary, the residential coal combustion was the most important source of PAHs, especially they emitted a large amount of PAHs in Aitken mode which led to the terrible air quality and high level of health risk. Therefore, the environmental protection measures should be tightened in such rural areas of north China.

Pyrolysis of excavated waste from landfill mining: Characterisation of the process products

The current transition to a circular economy model laid the foundations for the development of the Enhanced Landfill Mining concept. Hitherto, a few studies have been performed on the thermochemical valorisation of excavated waste, of which a majority concern incineration or gasification. Nonetheless, no previous studies on excavated waste pyrolysis, including the characterisation of the process products, have been identified. Ergo, this study aims at filling this knowledge gap. The pyrolysis of refuse-derived fuel formed from excavated waste was performed in a lab-scale reactor in the temperature range of 400–700 °C. The non-condensable products (non-condensables) were analysed using Micro GC, whereas the condensable products (condensables) were characterised using GC/MS. Additionally, the distribution of C, H, N, S, O, and Cl among the process products was analysed. The high content of C2–C3 hydrocarbons was detected in non-condensables, whereas the abundance of polycyclic aromatic hydrocarbons (PAHs) was detected among condensable products. However, due to feedstock complex thermal decomposition pattern, no overall tendency, covering the process product properties in relation to the process temperature, can be determined. These fluctuations of composition, therefore, have to be taken into account in the planning of the future utilisation of the excavated waste pyrolysis products. Moreover, two possible risks, connected with the further process products utilisation, were identified – namely, chlorine forming primarily organic compounds and sulphur forming mostly gaseous compounds (H2S).

Characterization and health risk assessment of particulate-bound polycyclic aromatic hydrocarbons in Tehran, Iran

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous pollutants in the urban atmosphere. An investigation of PAHs in the urban atmosphere of Tehran, Iran, was conducted in this study. Car engine air filters (CAFs) were collected in 15 taxi garages between 2016 and 2017 and analyzed for PAHs to assess the concentration level and health risks of polycyclic aromatic hydrocarbons (PAHs). The total concentrations of 16 PAHs (ΣPAHs) ranged from 169 to 174 μg/CAF. The average ΣPAHs concentration in winter was slightly higher than in summer. The most abundant individual PAH was phenanthrene, followed by fluoranthene, pyrene, and naphthalene. Concentrations of benzo[a]pyrene (BaP) varied between 1.80 and 2.27 μg/CAF. Based on estimated air volumes that pass through each CAF, atmospheric PAHs were estimated. ΣPAHs ranged from 8.31 to 8.39 ng/m3 for the average air volume estimate, less than those reported before using a high volume air sampler. The total carcinogenic risk of 16 PAH compounds was less than the acceptable limit of EPA for human health (1 × 10−6).

Emerging concerns of VOCs and SVOCs in coking wastewater treatment processes: Distribution profile, emission characteristics, and health risk assessment

In this study, the distribution profiles, emission characteristics, and health risks associated with 43 volatile and semi-volatile organic compounds, including 15 phenols, 18 polycyclic aromatic hydrocarbons (PAHs), 6 BTEX, and 4 other compounds, were determined in the wastewater treatment plant (WWTP) of a coking factory (plant C) and the succeeding final WWTP (central WWTP). Total phenols with a concentration of 361,000 μg L−1 were the predominant compounds in the influent wastewater of plant C, whereas PAHs were the major compounds in the final effluents of both coking WWTPs (84.4 μg L−1 and 30.7 μg L−1, respectively). The biological treatment process in plant C removed the majority of volatile organic pollutants (94.1%–99.9%). A mass balance analysis for plant C showed that biodegradation was the main removal pathway for all the target compounds (56.6%–99.9%) except BTEX, chlorinated phenols, and high molecular weight (MW) PAHs. Chlorinated phenols and high MW PAHs were mainly removed via sorption to activated sludge (51.8%–73.2% and 60.2%–75.9%, respectively). Air stripping and volatilization were the dominant mechanisms for removing the BTEX compounds (59.8%–73.8%). The total emission rates of the detected volatile pollutants from plant C and the central WWTP were 1,640 g d−1 and 784 g d−1, respectively. Benzene from the equalization basins of plant C and the central WWTP corresponded to the highest inhalation carcinogenic risks (1.4 × 10−3 and 3.2 × 10−4, respectively), which exceeded the acceptable level for human health (1 × 10−6) recommended by the United States Environmental Protection Agency. The results showed that BaP exhibited the highest inhalation non-cancer risk, with a hazard index ratio of 70 and 30 for plant C and the central WWTP, respectively. Moreover, the excess sludge generated during wastewater treatment should also be carefully handled because it adsorbed abundant PAHs and chlorinated phenols at coking plant C (58,000 μg g−1 and 3,500 μg g−1) and the central WWTP (622 μg g−1 and 54 μg g−1).

The Age Dependence of Mid-infrared Emission around Young Star Clusters

Abstract Using the star cluster catalogs from the Hubble Space Telescope program Legacy Extragalactic UV survey (LEGUS) and 8 μm images from the IRAC camera on the Spitzer Space Telescope for five galaxies within 5 Mpc, we investigate how the 8 μm dust luminosity correlates with the stellar age on the 30–50 pc scale of star-forming regions. We construct a sample of 97 regions centered at local peaks of 8 μm emission, each containing one or more young star cluster candidates from the LEGUS catalogs. We find a tight anticorrelation with a Pearson correlation coefficient of r = −0.84 ± 0.05 between the mass-normalized dust-only 8 μm luminosity and the age of stellar clusters younger than 1 Gyr; the 8 μm luminosity decreases with increasing age of the stellar population. Simple assumptions on a combination of stellar and dust emission models reproduce the observed trend. We also explore how the scatter of the observed trend depends on assumptions of stellar metallicity, polycyclic aromatic hydrocarbon (PAH) abundance, fraction of stellar light absorbed by dust, and instantaneous versus continuous star formation models. We find that variations in stellar metallicity have little effect on the scatter, while PAH abundance and the fraction of dust-absorbed light bracket the full range of the data. We also find that the trend is better explained by continuous star formation, rather than instantaneous burst models. We ascribe this result to the presence of multiple star clusters with different ages in many of the regions. Upper limits of the dust-only 8 μm emission as a function of age are provided.

Dietary intake of polycyclic aromatic hydrocarbons (PAHs) from coral reef fish in the Persian Gulf — Human health risk assessment

The present study investigated accumulation of petrogenic polycyclic aromatic hydrocarbons (∑39PAHs) in the livers and muscles of three coral-reef fish (50 specimens) from the Persian Gulf, Kharg Island (Iran), specifically Lethrinus microdon (n = 18), Lutjanus argentimaculatus (n = 17), and Scomberomorus guttatus (n = 15). For all fish, PAHs originated mostly from petroleum and combustion sources. Concentrations of ∑39PAHs were 1004 ngg−1 freeze-dried weight (fdw) and 1390 ngg−1 fdw for liver and muscle, respectively. The biota-sediment accumulation factor of 20,181 and equivalent concentrations of ∑PAHs (liver) were highest for L. argentimaculatus. Most of the abundant PAHs identified were low molecular weight (LMW-PAH) (liver > muscle) with 2–3 aromatic ring. Results for the human health risk assessment concluded the probability of PAHs intake via fish consumption was considerable in this area (lifetime cancer risk (ILCR) > 1 × 10−5; hazard quotients (HQs) > 1; hazard index (HI) ≈6; the excess cancer risk (ECR) > 1 × 10−6) and, therefore, comprehensive management and long-term monitoring is needed.

Teratogenic effects of environmentally relevant concentrations of phenanthrene on the early development of marine medaka (Oryzia melastigma)

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous pollutants in marine environments and have arouse great concern since they pose adverse effects to marine ecosystem. To determine the potential impacts of environmentally relevant PAHs on early life stages of marine fish, this study exposed embryos of marine medaka (Oryzias melastigma) to 0, 2, 10, 50, and 250 μg/L of phenanthrene (Phe), one of the most abundant PAHs. The results demonstrated that Phe exposure decreased hatching rates, delayed hatching time of embryos, and increased deformity rate of newly-hatched larvae. Exposure to 10 and 50 μg/L Phe decreased the survival rate of marine medaka larvae at 28 days post-fertilization (dpf), and no embryo successfully hatched in 250 μg/L Phe exposure group. Morphology results showed that 10, 50, and 250 μg/L Phe exposure significantly retarded the development of embryos, and 2, 10, and 50 μg/L caused yolk sac edema and pericardial edema in newly-hatched larvae, indicating that low concentrations of Phe could induce developmental cardiac toxicity. Furthermore, the changes in the expression of heart development-related genes were determined, and the results showed that Phe-induced cardiac malformation might be related with fgf8, bmp4, smyd1, ATPase and gata4 genes. Overall, environmentally relevant PAHs could disrupt heart morphogenesis and hatching process of marine medaka, which might have profound consequences for sustainability of fish population.

In vivo and in vitro inflammatory responses to fine particulate matter (PM2.5) from China and California

Ambient PM2.5 was collected during the winter season from Taiyuan, Shanxi, China; Jinan, Shandong, China; and Sacramento, California, USA, and used to create PMSX, PMSD, and PMCA extracts, respectively. Time-lag experiments were performed to explore the in vivo and in vitro toxicity of the PM extracts. In vivo inflammatory lung responses were assessed in BALB/c mice using a single oropharyngeal aspiration (OPA) of PM extract or vehicle (CTRL) on Day 0. Necropsies were performed on Days 1, 2, and 4 post-OPA, and pulmonary effects were determined using bronchoalveolar lavage (BAL) and histopathology. On Day 1, BAL neutrophils were significantly elevated in all PM- versus CTRL-exposed mice, with PMCA producing the strongest response. However, histopathological scoring showed greater alveolar and perivascular effects in PMSX-exposed mice compared to all three other groups. By Day 4, BAL neutrophilia and tissue inflammation were resolved, similar across all groups. In vitro effects were examined in human HepG2 hepatocytes, and U937 cells following 6, 24, or 48 h of exposure to PM extract or DMSO (control). Luciferase reporter and quantitative polymerase chain reaction assays were used to determine in vitro effects on aryl hydrocarbon receptor (AhR) activation and gene transcription, respectively. Though all three PM extracts activated AhR, PMSX produced the greatest increases in AhR activation, and mRNA levels of cyclooxygenase-2, cytochrome P450, interleukin (IL)-8, and interleukin (IL)-1β. These effects were assumed to result from a greater abundance of polycyclic aromatic hydrocarbons (PAHs) in PMSX compared to PMSD and PMCA.

The epitranscriptomic writer ALKBH8 drives tolerance and protects mouse lungs from the environmental pollutant naphthalene

ABSTRACT The epitranscriptomic writer Alkylation Repair Homolog 8 (ALKBH8) is a transfer RNA (tRNA) methyltransferase that modifies the wobble uridine of selenocysteine tRNA to promote the specialized translation of selenoproteins. Using Alkbh8 deficient (Alkbh8def) mice, we have investigated the importance of epitranscriptomic systems in the response to naphthalene, an abundant polycyclic aromatic hydrocarbon and environmental toxicant. We performed basal lung analysis and naphthalene exposure studies using wild type (WT), Alkbh8de f and Cyp2abfgs-null mice, the latter of which lack the cytochrome P450 enzymes required for naphthalene bioactivation. Under basal conditions, lungs from Alkbh8def mice have increased markers of oxidative stress and decreased thioredoxin reductase protein levels, and have reprogrammed gene expression to differentially regulate stress response transcripts. Alkbh8def mice are more sensitive to naphthalene induced death than WT, showing higher susceptibility to lung damage at the cellular and molecular levels. Further, WT mice develop a tolerance to naphthalene after 3 days, defined as resistance to a high challenging dose after repeated exposures, which is absent in Alkbh8def mice. We conclude that the epitranscriptomic writer ALKBH8 plays a protective role against naphthalene-induced lung dysfunction and promotes naphthalene tolerance. Our work provides an early example of how epitranscriptomic systems can regulate the response to environmental stress in vivo.