Abundant Polycyclic Aromatic Hydrocarbons Research Articles

Environmental impact and human health risk assessment of polycyclic aromatic hydrocarbons (pahs) in raw milk from free-ranging cattles in northwest nigeria.

Polycyclic aromatic hydrocarbons (PAHs) were determined in raw milk from Northwest Nigerian cattle (cow, goat and sheep) as indicators in assessing the current pollution status of the region. In Northwest Nigeria, most animals are free rangers with the likelihood that PAHs have been taken up by these animals on the process of drinking PAHs contaminated surface waters, eating road-side grasses, and soils. A total of 42 composite milk samples were collected by milking 3-5 animals. PAHs were extracted after saponification of the milk fats through sonication using dichloromethane/hexane mixture and the five ascertained most abundant PAHs are: Phe > BaP > Chr > Fla. > Pyr using gas chromatography-flame ionization detector (GC-FID). The diagnostic ratios showed that combustion is the major pathway of PAHs emission in the study area which judging from the economic level of the area, could be attributed to vehicular exhaust emission, use of firewood, industrial fumes, waste incineration and bush burning at the beginning of the farming season. The values of PAHs showed no significant variations (p > 0.05), either between the milk types (cow, goat and sheep) or between the seven states' milk samples, indicating a similar source of the PAHs. The European Food Safety Authority set 2μg/kg w/w BaP as a marker for the occurrence of PAHs contamination and assessment of likely effect of carcinogenic PAH in foodstuffs, the value of BaP obtained was however much higher even though raw milk is about 80% water. Most PAHs have carcinogenic effects on humans and induce various cancers. Therefore there should be a reduction in the bush burning at the beginning of the farming season, use of firewood and other pronounced sources of PAHs in the region.

Hierarchical Nanoporous C/C Composite from Humic Fulvic Acid and Sulfonated Pitch for High‐Energy‐Density EDLC Electrodes

AbstractAs a new type of energy storage device, electric double layer capacitors (EDLCs) possess fast charge/discharge speed and good cycling stability. However, the low energy density and high production cost of EDLC electrodes are still big challenges. Herein, a hierarchical nanoporous C/C composite is synthesized by chemical recombination and subsequent activation strategy from low‐cost carbon resources, namely renewable humic fulvic acid (FA) and industrial sulfonated pitch (SP). Profiting from the abundant polycyclic aromatic hydrocarbons in SP and plentiful oxygen‐containing groups in FA, the resultant nanoporous C/C composite has both high e‐conductivity and high specific surface area (SSA). Thus, this porous C/C composite can be directly fabricated as EDLC electrode without any conductive agent. By fully exploiting the synergistic effect between high e‐conductivity and high SSA, it shows excellent electrochemical stability in EMIMBF4 ionic liquid electrolyte. Furthermore, it possesses a higher specific gravimetric capacitance (117 F g−1) than that of pure FA‐based porous carbon (92.5 F g−1) at a current density of 1 A g−1. More importantly, the maximum energy density can be as high as 55.4 Wh kg−1, largely better than commercial activated carbon.

Occurrence and source apportionment of polycyclic aromatic hydrocarbons (PAHs) in dust of an emerging industrial city in Iran: implications for human health.

Polycyclic aromatic hydrocarbons (PAHs) bounded to street dust are a severe environmental and human health danger. This study provides preliminary information on the abundance of PAHs in street dust from Rafsanjan city, Iran, where industrial emissions are high and data are lacking. Seventy street dust samples were collected from streets with different traffic loads. The United States Environmental Protection Agency (USEPA) Standard Methods 8270D and 3550C were used for the measurement of PAHs using GC mass spectroscopy. The total concentration of PAHs was 1443 ng g-1, with a range of 1380-1550 ng g-1. Additionally, the concentration of carcinogenic PAHs (∑carcPAHs) ranged from 729.5 to 889.4 ng g-1, with a mean value of 798.1 ng g-1. Pyrene was the most abundant PAH, with an average concentration of 257 ng g-1. Source identification analyses showed that vehicle emissions along with incomplete combustion and petroleum were the main sources of PAHs. The ecological risk status of the studied area was moderate. Spatial distribution mapping revealed that the streets around the city center and oil company had higher PAH levels than the other sectors of Rafsanjan. The results indicated that dermal contact and ingestion of contaminated particles were the most important pathways compared to inhalation. The mean incremental lifetime cancer risk (ILCR) was 1.4 × 10-3 and 1.3 × 10-3 for children and adults, respectively. This implies potentially adverse health effects in exposed individuals. The mutagenic risk for both subpopulations was approximately 18 times greater than the one recommended by USEPA. Our findings suggest that children are subjected to a higher carcinogenic and mutagenic risk of PAHs, especially dibenzo[a,h]anthracene (DahA), bounded to street dust of Rafsanjan. Our study highlights the need for the development of emission monitoring and control scenarios.

Effects of fluoranthene on digestive enzymes activity and relative growth rate of larvae of lepidopteran species, Lymantria dispar L. and Euproctis chrysorrhoea L.

Fluoranthene is one of the most abundant polycyclic aromatic hydrocarbon pollutants in the environment and it may accumulate in plant leaves which are the main food source for phytophagous insect species. The aim of this study was to establish the effects of dietary fluoranthene on specific activities of digestive enzymes and expression of their isoforms in the midgut, and the relative growth rates of Lymantria dispar and Euproctis chrysorrhoea larvae. Exposure to fluoranthene led to significantly decreased trypsin activity in the midgut of larvae of both species. Leucine aminopeptidase activity decreased significantly in the midgut of L. dispar larvae exposed to the lower concentration of fluoranthene, but that enzyme activity showed the opposite trend in E. chrysorrhoea larvae. There was no pollutant induced changes in lipase activity in L. dispar, while elevated enzyme activity was recorded in the midgut of E. chrysorrhoea larvae exposed to the lower concentration of fluoranthene. Different patterns of expression of enzyme isoforms were noticed. Relative growth rates of both species significantly decreased in fluoranthene treated larvae. These responses indicate to the significance of relationships between physiological changes and fitness-related traits in L. dispar and E. chrysorrhoea larvae affected by pollutant, and contribute to understanding the mechanisms of their adjustment to stressful conditions.

Abundance of Polycyclic Aromatic Hydrocarbons (PAHs) in ground water of coastal areas at Sundarban; removal strategy and remediation

The confluence of various rivers, swamp forests, salty water abundance makes Sundarban a quite vulnerable ecosystem. This part of the delta areas suffers heavily from fresh water scarcity due to its increased salinity in river bed and polycyclic aromatic hydrocarbons (PAHs)/polyaromatic hydrocarbons/polynuclear aromatic hydrocarbons. PAHs are generally insoluble and found as contaminants in drinking water produced from burning coal, gasoline, trash, tobacco, wood etc. Samples of ground water have been found with more than ten different variants of PAHs by gas chromatography equipment with large amount of dissolved salts which are harmful for human health. A conventional activated carbon packed bed type treatment process has been used to purify the contaminated organic rich raw water by the adsorptive surface contact method of bed. In order to remove fine particles leaching out of the packed bed filter, an ultrafiltration membrane was used to reject those substances which are producing turbidity, such as fine particles, colloids, algae remaining in the water. Total dissolved solids and the PAHs of the ground water reduced significantly by the dual process and further this combination may be used for effective separation of PAHs and cost effective drinking water production.

Variability in urinary biomarkers of human exposure to polycyclic aromatic hydrocarbons and its association with oxidative stress.

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous environmental pollutants. Urinary concentrations of mono-hydroxylated metabolites of PAHs (OH-PAHs) have been used as biomarkers of these chemicals’ exposure in humans. Little is known, however, with regard to intra- and inter-individual variability in OH-PAH concentrations and their association with oxidative stress. We conducted a longitudinal study of measurement of urinary concentrations of 15 OH-PAHs and 7 oxidative stress biomarkers (OSBs) of DNA damage [8-hydroxy-2′-deoxyguanosine (8-OHdG)], lipid [malondialdehyde (MDA) and F2-isoprostanes (PGF2α)] and protein [o,o′ -dityrosine (diY)] peroxidation in 19 individuals for 44 consecutive days. Metabolites of naphthalene (OHNap), fluorene (OHFlu), phenanthrene (OHPhe), and pyrene (OHPyr) were found in >70% of 515 urine samples analyzed, at sum concentrations (∑OH-PAH) measured in the range of 0.46–60 ng/mL. After adjusting for creatinine, OHNap and ∑OH-PAH concentrations exhibited moderate predictability, with intra-class correlation coefficients (ICCs) ranging from 0.359 to 0.760. However, ICC values were low (0.001–0.494) for OHFlu, OHPhe, and OHPyr, which suggested poor predictability for these PAH metabolites. Linear mixed-effects analysis revealed that an unit increase in ∑OH-PAH concentration corresponded to 4.5%, 5.3%, 20%, and 21% increase in respective urinary 8-OHdG, MDA, PGF2α, and diY concentrations, suggesting an association with oxidative damage to DNA, lipids, and proteins. The daily intakes of PAHs, calculated from urinary concentrations of OH-PAHs, were 10- to 100-fold below the current reference doses. This study provides valuable information to design sampling strategies in biomonitoring studies and in assigning exposure classifications of PAHs in epidemiologic studies.

Intermediate-size fullerenes as degradation products of interstellar polycyclic aromatic hydrocarbons

The high interstellar abundances of polycyclic aromatic hydrocarbons (PAHs) and their size distribution are the result of complex chemical processes implying dust, UV radiation, and the main gaseous components (H, C+, and O). These processes must explain the high abundance of relatively small PAHs in the diffuse interstellar medium (ISM) and imply the continuous formation of some PAHs that are small enough (number of carbon atoms NC < ~35–50) to be completely dehydrogenated by interstellar UV radiation. The carbon clusters Cn thus formed are constantly exposed to the absorption of ~10–13.6 eV UV photons, allowing isomerization and favoring the formation of the most stable isomers. They might tend to form irregular carbon cages. The frequent accretion of interstellar C+ ions could favor further cage isomerization, as is known in the laboratory for C60, possibly yielding most stable fullerenes, such as C40, C44, and C50. These fullerenes are expected to be very stable in the diffuse ISM because C2 ejection is not possible by single UV photon absorption, but could need rare two-photon absorption. It is possible that at least one of these fullerenes or its cation is as abundant as C60 or C60+ in the diffuse ISM, although this abundance is limited by the lack of observed matching features in observed mid-infrared spectra. B3LYP calculations of the visible spectrum for a number of fullerene isomers with 40 ≤NC ≤ 50 show that they generally have a few spectral bands in the visible range, with f-values in the range of a few 10−2. This could make such fullerenes interesting candidates for the carriers of some diffuse interstellar bands.

Polycyclic aromatic hydrocarbons and their relationship to maturity and paleoenvironmental settings in lacustrine sediments of the Neogene Toplica Basin, Serbia

The study investigated the influence of maturity, biomass type, and depositional settings on the distribution and relative abundance of polycyclic aromatic hydrocarbons (PAHs) for lacustrine sediments collected from depths up to 1000 m of Prebreza and Čučale stratigraphic units (the northwest part of the Toplica Basin). A recently proposed benzo[ghi]perylene/(perylene + benzo[ghi]perylene) parameter, along with commonly used Phenanthrene Alkylation Index and benzo[e]pyrene/(perylene + benzo[e]pyrene) indices, pointed out differences in maturity levels between stratigraphic units by displaying a positive linear relationship with vitrinite reflectance. However, in several immature Prebreza sediments, a substantial presence of algae and/or anoxic, mesosaline/hypersaline conditions were suitable for forming β-substituted methylphenanthrenes and 6-ring benzo[ghi]perylene. Generally, high molecular weight unsubstituted PAHs (HMWPAHs), particularly perylene, predominated Prebreza sediments. Anoxic conditions appeared to be decisive for accumulating and preserving the perylene carbon skeleton in studied stratigraphic units. Besides, more intense volcanism in the Čučale unit favored combustion processes, which prompted the accumulation of low molecular weight unsubstituted PAHs (LMWPAHs), especially phenanthrene. A general prevalence of retene over cadalene in Prebreza sediments, in which alginite and liptodetrinite predominated, implied algae as retene precursor. Selective degradation of retene or hindered demethylation of 9-methylphenanthrene under anoxic and more saline environmental settings had occurred notably in the Prebreza unit, which led to the formation of 1-methylphenanthrene and/or pimanthrene (1,7-dimethylphenanthrene). Čučale sediments with substantial amounts of vitrinite macerals or saturated diterpenoids had a predominant simonellite derived from conifers. Non-degraded and well-preserved Pinaceae conifers predominated in Prebreza sediments deposited under semi-arid climatic conditions, whereas mixed degraded/non-degraded conifers characterized Čučale sediments deposited in a wide range of climatic conditions, from semi-arid to semi-humid.

A comprehensive kinetic study on the speciation from propylene and propyne pyrolysis in a single-pulse shock tube

This work is centered on the speciation from propylene and propyne pyrolysis by means of shock tube experiments and detailed kinetic modeling. A wealth of intermediates and products, covering small acyclic hydrocarbons up to four-ring aromatics, are probed from the C3 fuels pyrolysis at a nominal pressure of 20 bar over 1050–1650 K. With updates in reactions involving C3 species, our on-going polycyclic aromatic hydrocarbon (PAH) formation kinetic model can well predict the measurements obtained in the current work as well as relevant literature data. Propyne exhibits a unique two-stage decomposition profile, as the characteristic isomerization to allene dominates in its consumption at moderate temperatures below 1300 K. Overall, propylene pyrolysis results in more diverse small hydrocarbons, but much lower contents of aromatics, in comparison to propyne pyrolysis. In both studied cases, the formation of benzene is dependent upon the propargyl recombination, and since propyne decomposition induces a more rapid and more plentiful propargyl production, benzene mole fractions are much higher in propyne pyrolysis. In both cases, naphthalene is observed as the most abundant PAH species, followed by acenaphthalene. Modeling analyses indicate that similar reaction pathways are responsible for the PAH formation in propylene and propyne pyrolysis. Indene is formed from the interactions between benzene/phenyl and C3 species, through its non-PAH isomers as intermediates. The subsequent reactions of indenyl radical with methyl and propargyl are essential pathways leading to naphthalene and acenaphthalene, respectively. Naphthyl radical further participates in the formation of different larger PAHs. The methylene-substituted cyclopenta-ring species are deemed as important precursors of their aromatic isomers, as is noted from the fulvene-to-benzene, benzofulvene-to-naphthalene and 9-methylene-fluorene-to-phenanthrene conversions.

Evaluation of Oxidative Potential of Pyrenequinone Isomers by the Dithiothreitol (DTT) Assay

Atmospheric quinoid polycyclic aromatic hydrocarbons (PAHQs) have adverse health effects as redox-active species in particulate matter (PM). Several PAHQs are known to be very reactive in the dithiothreitol (DTT) assay; however, it is unclear if pyrenequinones, their parent pyrene is one of the most abundant polycyclic aromatic hydrocarbons (PAHs) in the atmosphere, contribute to the loss of DTT in PM extracts. Herein, by employing the DTT assay, we evaluated oxidative potentials of three pyrenequinone isomers (4,5-pyrenequinone [4,5-PyQ] and a mixture of 1,6-/1,8-pyrenequinones [1,6-/1,8-PyQ]), along with 9,10-phenanthrenequinone (PQN), 1,2-naphthoquinone (1,2-NQ), and 1,4-naphthoquinone (1,4-NQ), of which DTT loss rates were examined previously. Our results demonstrate that the DTT consumption by ortho-type PAHQs is fast, particularly by 4,5-PyQ. The order of DTT loss rate by the PAHQs tested in this study was as follows: 4,5-PyQ ∼ PQN > 1,2-NQ > 1,4-NQ ∼ 1,6-/1,8-PyQ. 4,5-PyQ was confirmed to be active in the DTT assay for the first time in this study. The DTT consumption rate by 4,5-PyQ is 14.6 ± 0.8 mol/min/PAHQ-mol, which is comparable to that of PQN (14.4 ± 0.1 mol/min/PAHQ-mol) known as the most active PAHQs by the DTT assay so far.

Removal of naphthalene and phenanthrene in synthetic solutions by electro-oxidation coupled with membrane bioreactor.

Naphthalene (NAPH) and phenanthrene (PHEN) are two of the most abundant polycyclic aromatic hydrocarbons (PAHs) found in nature, and they are considered in the list of US EPA priority pollutants. The contribution of this research lies in the comprehensive analysis of a strategy for the coupling of electro-oxidation (EO) and biodegradation in a submerged membrane bioreactor (SMBR) with the objective to remove PAHs, using NAPH and PHEN as model compounds. The electrochemical degradation of NAPH and PHEN in aqueous synthetic solution has been carried out using two different anodes: Ti/IrO2 and Ti/SnO2. The effects of EO operating parameters (current density, reaction time, and pH) on the NAPH and PHEN removals were investigated applying 23 factorial design with both electrodes. Additionally, the EO effluents were analyzed for COD, NH4-N, and biodegradability (respirometry tests). The highest removals of both compounds were reached with Ti/IrO2 anode, at acidic conditions (pH of 2), current density of 50 mA cm-2, and electrolysis time of 60 min. However, the Ti/SnO2 anode allowed greater reduction of the biomass inhibition, which means that the enhancement of the EO effluent biodegradability was reached; therefore, this electrode was selected for the coupled EO-SMBR system, applying the operating conditions that improved the biodegradability of the effluent. The EO process allowed NAPH and PHEN removal efficiencies of 96 ± 5% and 94 ± 3%, respectively. The membrane bioreactor was operated with organic load of 0.6 ± 0.1 gCOD gVSS-1 d-1, hydraulic retention time of 6 h, and solid retention time of 30 d, obtaining average COD, NH4-N, NAPH, and PHEN removals of 98±0.5%, 91±6.4%, 99.1±0.96%, and 99.7±0.4% respectively. The sorption of phenanthrene onto the biomass had a low contribution, 0.9±0.2%, concluding that biodegradation was the main removal mechanism in the bioreactor. The coupled system EO-SMBR allowed high NAPH and PHEN removal efficiencies of 99.99±0.01 and 99.99±0.02%, respectively.

Bioaccumulation of legacy organic contaminants in pregnant Indo-Pacific humpback dolphins (Sousa chinensis): Unique features on the transplacental transfer

The placental transfer and congener composition of organic contaminants (OCs) in Indo-Pacific humpback dolphins have been little studied. In the present study, 16 polycyclic aromatic hydrocarbons (PAHs), 18 organochlorine pesticides (OCPs), and 28 polychlorinated biphenyl (PCB) congeners were analyzed in muscle, lung, liver, kidney, and blubber tissues from three mother–fetus pairs of this species stranded along the Pearl River Estuary, China. For PCBs, tetra-, penta-, hexa-, and hepta-chlorobenzene congeners were dominant in all the analyzed samples. Among them, hexachlorobenzene congeners showed the highest level in most dolphin mother-fetus tissue samples. The concentrations of PCBs and OCPs in adult females were higher in the detoxification organs (liver and kidneys) than in the muscles and lungs, whereas muscle tissues in fetuses generally exhibited higher PCBs and OCPs levels than the livers and kidneys. The most abundant PAHs in the four tissues were those with lower molecular weights, which were also the most water-soluble and bioavailable. Negative correlations between the octanol/water partition coefficients (log KOW) and the fetus/mother ratios for PCB congeners revealed that the transfer of PCBs may be determined by their lipid solubility. OCPs and PCBs with low molecular weights and low log KOW values would be more likely to accumulate in the dolphin liver, lung, kidney and muscle tissues. Furthermore, OCs with low molecular weights and low log KOW values were more concentrated in the fetal blubber, lung, and liver tissues than in their respective mothers. The ubiquitous existence of OCs in the mother–fetus pairs strongly suggested that these contaminants could pass through the placenta and partition in fetal tissue. The high transfer efficiency of PAHs and PCBs indicated that the placenta might not be an efficient barrier for these pollutants. PCBs levels in both mother and fetus dolphins could cause immunosuppression.

Late Miocene C4 Grassland Fire Feedbacks on the Indian Subcontinent

AbstractFire dynamics potentially account for the asynchronous timing of the expansion of C4 grasslands throughout the Mio‐Pliocene world. Yet how fire, climate, and ecosystems interacted in different settings remain poorly constrained because it is difficult to quantify fires and fuel source over these timescales. Here, we apply molecular proxies for fire occurrence alongside records of vegetation change and paleohydrology in Bengal Fan sediments (ODP Leg 116) to examine fire feedbacks on the south Asian continent. We employ abundances of polycyclic aromatic hydrocarbons (PAHs) to reconstruct fire occurrence and δ13C measurements of pyrogenic PAHs to constrain fuel source and grassland burning. This combination allowed us to test whether: (1) a fire‐seasonality forcing facilitated the expansion of grassland ecosystems and (2) a fire‐C4 grass burning feedback maintained these systems. PAHs can be sourced from weathered fossil carbon (i.e., a petrogenic source) and from burned terrestrial biomass (i.e., a pyrogenic source). Alkylated and non‐alkylated structure abundance data distinguished pyrogenic from petrogenic sourced samples. A sharp increase in pyrogenic PAHs along with increases in δ2H and δ13C values of plant waxes at 7.4 Ma indicates increased fire coincided with the onset of C4 expansion and hydrologic change in South Asia. The correlated 13C enrichment in PAHs, 13C enrichment in plant waxes, and increased abundances of PAHs suggest burning of C4 grasslands likely maintained open ecosystems. Our results link fire to the initial opening of grassland ecosystems on a subcontinental‐scale and support disturbance as a critical mechanism of terrestrial biome transition.

Long-term exposure to environmental level of phenanthrene causes adaptive immune response and fibrosis in mouse kidneys

As ubiquitous, persistent organic pollutants, polycyclic aromatic hydrocarbons (PAHs) have adverse impacts on human health. Phenanthrene (Phe) is one of the most abundant PAHs in the environment. However, the long-term effects of exposure to environmental level of Phe on the kidneys and the potential mechanisms are unclear. T helper (Th) cells, a subtype of CD4+ T cells that play a central role in the renal immune microenvironment. In this study, male mice were chronically exposed to 5, 50, and 500 ng/kg bw Phe every other day for total 210 days. Those results indicated that environmental Phe exposure caused kidney hypertrophy, injury and fibrosis in the mice. Chronic, long-term environmental level of Phe exposure did not significantly alter the innate immune response but induced adaptive immune response changes (Th1/Th2 related cytokines release), causing a type 1 immune response in the 5 ng/kg bw Phe group and a type 2 immune response in the high dose groups (50 and 500 ng/kg bw). This study provides novel insights into the roles of adaptive immune response in long-term PAH exposure-induced chronic kidney injury and fibrosis, which is beneficial for further understanding the potential health hazards of PAHs and providing new avenues for immune intervention strategies to alleviate PAHs toxicity.

Environment impact and probabilistic health risks of PAHs in dusts surrounding an iron and steel enterprise

Dust can be regarded as environmental medium that indicates the level and spatial distribution of polycyclic aromatic hydrocarbons (PAHs) coming from different pollution sources. In this study, samples including road dust, roof dust, and bare soil near an iron and steel enterprise (ISE) in Laiwu city of North China were collected. To assess the environment impact, atmosphere particulates and one flue dust from a coking plant were simultaneously sampled. Sixteen USEPA PAHs were detected quantitatively by Gas Chromatography Mass Spectrometry (GC–MS). A laser particle size analyzer was used to obtain the grain size of the dust particle samples. The results showed that PAH concentrations displayed great variability in the dust samples. The ∑16PAHs concentration was found to be between 0.460 and 46.970 μg/g (avg ± sd 10.892 ± 1.185 μg/g) in road dust, between 0.670 and 17.140 μg/g (avg ± sd 6.751 ± 0.692 μg/g) in roof dust, and 13.990 ± 1.203 μg/g in bare soil. In the environment atmosphere sites, the ∑16 PAHs value in PM2.5 constituted a very large proportion of PM10, indicating that PAHs in finer particle sizes should be given greater emphasis. The ∑16PAHs concentration was relatively high in the area close to the ISE because of the great impact of the ISE industrial activities. PAH concentration curves were similar, and the most abundant individual PAHs in the atmosphere sites were BbF, BkF, and Flu, and BbF, BkF, and Chry in dusts. Toxicity analysis revealed that PAHs with four rings, including carcinogenic PAHs, were the dominant pollutants in the studied area. The toxic equivalency value (TEQBaP), the carcinogenic health risk assessment value recommended by the US EPA, was calculated for seven carcinogenic PAHs, revealing that they account for more than 93.0% of the total TEQBap of the 16 PAHs and indicating the major toxic equivalent concentration contributor. Incremental lifetime cancer risk (ILCR) estimation results showed that PAHs tended to bring about great health risks through skin contact, followed by ingestion and inhalation. By comparison, road dust exhibited greater carcinogenic risks than roof dust, and bare soil may undergo heavier pollution. Therefore, the results of this study would be helpful in the effort to understand the PAHs pollution from the steel industry, which will provide some guidance for the probabilistic assessment of local health risks.

Trends in urinary metabolites of polycyclic aromatic hydrocarbons (PAHs) in the non-smoking U.S. population, NHANES 2001–2014

BackgroundRecent studies indicate airborne PAH levels have decreased in the U.S., but it is unclear if this has resulted in PAH exposure changes in the U.S. population. ObjectiveExamine temporal trends in urinary metabolites of Naphthalene, Fluorene, Phenanthrene, and Pyrene in U.S. non-smokers, 6+ years old. MethodsWe used biomonitoring data from the National Health and Nutrition Examination Survey (NHANES) program, 2001–2014, (N = 11,053) using survey weighted linear regression. Models were adjusted for age, sex, race/ethnicity, creatinine, BMI, income, diet, and seasonality. Stratified models evaluated the effect of age, sex, and race/ethnicity on trends. ResultsBetween 2001 and 2014, Naphthalene exposure increased 36% (p < 0.01); Pyrene exposure increased 106% (p < 0.01); Fluorene and Phenanthrene exposure decreased 55% (p < 0.01), and 37% (p < 0.01), respectively. Naphthalene was the most abundant urinary PAH, 20-fold higher than Fluorene and Phenanthrene, and over 50-fold higher than Pyrene compared to reference groups, effect modification was observed by age (Naphthalene, Pyrene), sex (Fluorene, Pyrene), and race/ethnicity (Naphthalene, Fluorene, Phenanthrene, Pyrene). SignificanceThis study shows exposure to Naphthalene and Pyrene increased, while exposure to Fluorene and Phenanthrene decreased among the non-smoking U.S. general population between 2001 and 2014, suggesting environmental sources of PAHs have changed over the time period.

Polycyclic aromatic hydrocarbons in the Mukundpura (CM2) Chondrite

Soluble polycyclic aromatic hydrocarbons (PAHs) have been measured in Mukundpura (MK) CM2 carbonaceous chondrite using Gas Chromatography-Mass Spectrometry (GC-MS). The data show high yields of PAHs with the presence of 2, 3, and 4 ring polycyclic aromatic hydrocarbons along with heterocyclic nitrogen and sulfur-containing compounds. MK also shows the presence of significant amount of alkylation products. The distribution and relative abundances of PAHs in the MK are discussed in context of its petrographic grade and correlation with aqueous alteration.

Evaluation of Polycyclic Aromatic Hydrocarbons (PAHs) in Bamboo Shoots from Soil.

The toxicity, carcinogenicity and persistence of polycyclic aromatic hydrocarbons (PAHs) pose a great threat to the ecological system and human health. The contamination levels, translocation and source analysis of 16 PAHs in bamboo shoot and its planted soil were investigated. The average concentrations of total PAHs were 18.80 ± 1.90 µg/kg and 123.98 ± 113.36 µg/kg in bamboo shoots and soils, respectively. The most abundant PAH was Phenanthrene (PHE), with the detected average concentrations of 5.85 µg/kg in bamboo shoots and 19.28 µg/kg in soils. The highest detected types of PAHs were 3 rings and 4 rings, with the proportions of 80.69% (bamboo shoots) and 35.23% (soils). The transfer factors of PAHs were ranged from 0.011 to 0.895, in which PAHs with 3 rings showed the strongest transfer ability. The combustion of biomass and petroleum might be the main source of PAHs in the planted soils of bamboo shoots.

Role of Polycyclic Aromatic Hydrocarbons on the Cosmic-Ray Ionization Rate in the Galaxy

Abstract The cosmic-ray (CR) ionization rate (ζ, s−1) plays an important role in the interstellar medium. It controls ion–molecular chemistry and provides a source of heating. Here we perform a grid of calculations using the spectral synthesis code CLOUDY along nine sightlines toward, HD 169454, HD 110432, HD 204827, λ Cep, X Per, HD 73882, HD 154368, Cyg OB2 5, and Cyg OB2 12. The value of ζ is determined by matching the observed column densities of H 3 + and H2. The presence of polycyclic aromatic hydrocarbons (PAHs) affects the free electron density, which changes the H 3 + density and the derived ionization rate. PAHs are ubiquitous in the Galaxy, but there are also regions where PAHs do not exist. Hence, we consider clouds within a range of PAH abundances and show their effects on the H 3 + abundance. We predict an average CR ionization rate for H2 (ζ(H2)) = (7.88 ± 2.89) × 10−16 s−1 for models with average Galactic PAH abundances, (PAH/H = 10−6.52), except Cyg OB2 5 and Cyg OB2 12. The value of ζ is nearly 1 dex smaller for sightlines toward Cyg OB2 12. We estimate the average value of ζ(H2) = (95.69 ± 46.56) × 10−16 s−1 for models without PAHs.

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.