High Molecular Weight Polycyclic Aromatic Hydrocarbons Research Articles

Influence of temperature and precipitation on the fate of polycyclic aromatic hydrocarbons: simulation experiments on peat cores from a typical alpine peatland in Central China.

The corresponding relationships between temperature, precipitation, and polycyclic aromatic hydrocarbon (PAH) concentration in a typical ombrotrophic peatland in Dajiuhu, Shennongjia, were quantitatively characterized by field sampling tests validated with simulation experiments. The PAH concentrations of peat cores in Dajiuhu peatland ranged from 262 to 977ng·g-1, with a mean value of 536 ± 284ng·g-1. PAHs were mainly composed of 2-3 ring PAHs, accounting for 31.7% ± 2.00% and 31.7% ± 5.00%, respectively. The concentration of PAHs in peat cores showed a significant decrease with increasing temperature, while the low molecular weight PAHs (LMW-PAHs) were more sensitive to temperature changes compared to the high molecular weight PAHs (HMW-PAHs). Besides, with the increase of quantity and velocity of leaching liquid, PAHs in peat were first transferred in the form of attached large-size particles and then gradually entered the aqueous phase. According to the IPCC projections of global warming, Dajiuhu peatland will release 956 ± 26.3kg·°C-1 PAHs into gas phase during 2030-2052, and a conservative projection based on local temperature trends showed that 459 ± 12.6kg·°C-1 PAHs will be released into gas phase by 2047 in Dajiuhu peatland. The projected release fluxes of PAHs in Dajiuhu peatland with precipitation volume and precipitation velocity are 381 ± 201kg·100mm-1 and 1052 ± 167kg·min·mL-1, respectively, which are primarily from peat into particulate and aqueous phase.

Enhancement of soil high-molecular-weight polycyclic aromatic hydrocarbon degradation by Fusarium sp. ZH-H2 using different carbon sources

High-molecular-weight PAHs (HMW-PAHs) in soil cannot be easily degraded. However, nutrient supplementation could stimulate the growth of exogenously added strains to enhance the degradation of HMW-PAHs in polluted soil. This study evaluated the applicability of Fusarium sp. ZH-H2, a polycyclic aromatic hydrocarbon (PAH)-degrading strain isolated by our research group, for the bioremediation of contaminated soil from the Hebei coal mining area in China. A soil incubation experiment was conducted to investigate the effect of two carbon sources and different carbon, nitrogen, and phosphorus (C:N:P) ratios on the remediation of high-molecular-weight PAHs (HMW-PAHs) in soil by Fusarium sp. ZH-H2, as well as the induction of lignin peroxidase activity. Our findings indicated that the HDF2 treatment (equal parts of humic acid and starch as carbon sources at a 50:1:0.5 C:N:P ratio) enhanced the removal rate of total HMW-PAHs from soil, reaching a maximum removal rate of 37.15 %. The removal rates of Pyr (a 4-ring PAH), BaP (a 5-ring PAH), and BghiP (a 6-ring PAH) were the highest in HDF2 treatment, and the removal rates were 39.51 %, 54.63 %, and 38.60 %, respectively. Compared with the ZH-H2 treatment, different carbon sources and C:N:P ratios significantly induced soil lignin peroxidase activity and the HDF2 treatment also resulted in the highest enzyme activity (up to 34.68 U/L). Furthermore, there was a significant or highly significant linear positive correlation between the removal rate of HMW-PAHs and enzyme activity in all cases. Our findings suggest that the optimal HMW-PAH degradation performance and enhancement of lignin peroxidase activity by ZH-H2 were achieved when both starch and humic acid were used as carbon sources at a C:N:P ratio of 50:1:0.5.

Pyrolysis temperature influences the capacity of biochar to immobilize copper and arsenic in mining soil remediation.

Biochar is a promising material used for multiple remediation approaches, mainly in polluted soils. Its properties can differ depending on feedstock and pyrolysis temperature. In this context, we tested the capacity of three biochar products made from corncob, pyrolyzed at different temperatures (350, 500, and 650°C), to remediate a mining soil affected by high levels of Cu and As. We performed an exhaustive characterization of the biochar. We found that biochar showed a higher surface area with increasing pyrolysis temperature, whereas high molecular weight PAHs were detected in biochar produced at the maximum temperature, thus indicating potential ecotoxicological risks. After the application of biochar to the soil, Cu was partially immobilized, especially when using that obtained at 500°C. This effect is attributed to the structure of this material and an increase in soil pH and organic matter content. Conversely, As was increased in the soluble fraction for all three types of biochar but in a proportion that lacks relevance. On the whole, given its lower PAH content, higher Cu immobilization ratio, and an almost negligible increase in As availability, biochar obtained at 500°C outperformed the other two products with respect to soil recovery. Of note, data on Cu and As availability were doubled-checked using two extraction methodologies. We propose that this operational approach for determining the most suitable pyrolysis temperature will find application in other soil remediation actions.

Determination of 16 particle-phase polycyclic aromatic hydrocarbons in herbal incense by ultrasonic extraction-gas chromatography-mass spectrometry and analysis of emission characteristics

Polycyclic aromatic hydrocarbons (PAHs) have attracted global attention because they are carcinogens and mutagenic to humans. To date, more than 200 PAHs have been found. The United States Environmental Protection Agency (USEPA) has designated 16 PAH species as priority control pollutants due to their highly toxic substances. Herbal incense is frequently used in daily life. As a result, it is critical to investigate its impact on human health and environmental safety. However, research on particle-phase PAHs is very limited and inapplicable. The current research focuses mainly on bamboo incense, which has a simpler formula than herbal incense.In this study, the emission factor and emission characteristics of particle-phase PAHs from herbal incense were described. A method combining ultrasonic and gas chromatography-mass spectrometry (GC-MS) was developed for the simultaneous determination of 16 particle-phase PAHs of herbal incense. The settings for extraction solvent, ultrasonic time, and instrument analysis conditions were optimized. In the test chamber, samples were collected by burning 0.8 g of herbal incense. After combustion, PAHs adsorbing on the particles of herbal incense were collected on a quartz filter. The whole filter sample was sliced and extracted with n-hexane-dichloromethane (1∶1, v/v). A rotary evaporator was used to concentrate the extract. GC-MS was used to analyze the prepared sample. The internal standard method was used to perform quantitative analysis on the target compounds. The linearities of the 16 target PAHs were good between mass concentrations of 0.1-5.0 μg/mL, with correlation coefficients greater than 0.998. The method detection limits (MDLs) of the 16 PAHs ranged from 0.4 to 3.8 ng/g. The 0.625 μg/g and 1.25 μg/g spiked recoveries ranged from 77.4% to 99.5% and 82.0% to 101.3%, respectively. The relative standard deviations (RSDs) of the 16 PAHs were ranged from 0.7% to 7.2% (n=6). The emission factors of particle-phase PAHs from five different kinds of herbal incense ranged from 4.60 to 11.89 μg/g. The highest concentration of phenanthrene (Phe) was found in 16 particle-phase individual PAHs of herbal incense. Fluoranthene (Flu), pyrene (Pyr), chrysene (Chr) and anthracene (Ant) concentration were ranked after Phe. The sum of these five proportions was 73.00%-89.97%. The proportion of Phe in herbal incense particle-phase PAHs was significantly higher than that of other indoor combustion sources. As a result, Phe could be used to identify individual PAHs in the particle-phase of herbal incense. The particle-phase PAHs were mainly distributed on the 3-ring and 4-ring, with a sum of 83.84% to 96.31% on the 3-ring and 4-ring. The proportion of high-molecular weight PAHs in the samples ranged from 44.25% to 63.31%. The proportion of low-molecular weight PAHs in the samples ranged from 36.69% to 55.75%. The incense source could be distinguished from other indoor combustion sources by its distinctive Phe/Flu ratio. The established method has high sensitivity, simple operation, and requires fewer samples. This method is suitable for rapidly detecting PAHs in burning incense. At the same time, it provides scientific data for further studies on the distribution and health effects of particle-phase PAHs of herbal incense.

Sedimentary PAH and oxidative stress biomarkers responses on Namalycastis abiuma (Polychaeta: Nereididae) from an urbanized Amazon estuary

Contamination by polycyclic aromatic hydrocarbons (PAH) in sediments and oxidative stress biomarkers responses (glutathione-S-transferase activity—GST and lipoperoxidation—LPO) on the polychaetes Namalycastis abiuma were screened along the urbanized margin of the Guajará Estuary, Brazilian Amazon coast, during dry and rainy seasons. Total 16 priority PAH concentrations ranged from 17 to 386 ng g−1 dry sediment, with higher values during the dry season. High molecular weight PAHs predominated during dry season and were probably originated from fossil fuel burning. Increased naphthalene and anthracene concentrations were noted when the maximum river flow was recorded and suggest diffuse sources from drainage of contaminated surfaces. Ecotoxicological PAH risks were low according to international sediment quality indices. Nevertheless, PAH toxicity equivalency was around 10-fold higher nearer the oil terminal than alongside the estuary. Highest GST activities at the oil terminal and industrial sites coincided with the rainy season, and combined with hydrochemical and sedimentary conditions thought to promote PAH bioavailability and a prolonged toxicant exposure. LPO approached similar levels in both seasons, suggesting that enzymatic activities were sufficient to uphold the prooxidants exposure. This result indicates that the overall estuarine condition exerts subtle oxidative stress on a keystone species and matches the low PAH ecotoxicological risks. Depositional margins within the mangrove areas and port operation are susceptible to an enhanced PAH accumulation and need special surveillance.

Characterizing the efficiency of low-cost LED lights for conducting laboratory studies to investigate polycyclic aromatic hydrocarbon photodegradation processes

Polycyclic aromatic hydrocarbons (PAHs) are common contaminants ubiquitously present in various waste products such as biosolids (e.g. wastewater sludges), oil spill residues (e.g. tarballs), road asphalts, and combustion byproducts. In this study, the photodegradation of PAHs is investigated under natural sunlight (cloudy and sunny/clear weather conditions), and using two types of artificial LED light sources. This is the first study to investigate the relative efficiency of low-cost LED light sources for conducting laboratory-scale PAH photodegradation experiments and directly comparing the results against those obtained using natural sunlight. Two types of LED light sources are investigated in this study: a light source with a full-spectrum range (380 nm–780 nm) that can cover the broad wavelength range of solar light reaching the Earth's surface, and a light source with a UV-A range (365 nm) that covers the UV range of the solar spectrum reaching the Earth's surface. The results show that the degradation of high molecular weight (HMW) PAHs is primarily due to photodegradation, and other lighter PAHs are degraded by both photodegradation and evaporation processes. HMW PAH photodegradation reactions follow the first-order degradation kinetics. The degradation rate constants of different PAHs are used to compare the relative efficiency of the light sources. The data show that the full-spectrum LED induced PAH photodegradation rates are similar to the natural sunlight induced rates. Furthermore, when the values of the rate constants are normalized to respective irradiance levels, the normalized rates for HMW PAH photodegradation under both full-spectrum LED light and natural sunlight are almost identical. However, the normalized photodegradation rate constants of HMW PAHs under the UV-A LED light are about two to three orders of magnitude higher than the sunlight as well as the full-spectrum-LED values. Therefore, the UV-A LED light is the optimal low-cost light source for studying PAH photodegradation processes under laboratory conditions.

Differences in adsorption, transmembrane transport and degradation of pyrene and benzo[a]pyrene by Bacillus sp. strain M1

In a previous study our group identified Bacillus sp. strain M1 as an efficient decomposer of high molecular weight-polycyclic aromatic hydrocarbons (HMW-PAHs). Interestingly, its removal efficiency for benzo[a]pyrene (BaP) was nearly double that of pyrene (Pyr), which was the reverse of what is reported for most other species. Here we compared the differential steps of biosorption, transmembrane transport and biodegradation of Pyr and BaP by strain M1 in order to assist in targeted selection of dominant strains and their degradation efficiency in the remediation of these two HMW-PAHs. The overall biosorption efficiency for BaP was 19% higher than that for Pyr, and the time needed to reach BaP peak adsorption efficiency was 4 days shorter than for Pyr. Transmembrane transport of the PAHs was compared in presence of sodium azide which inhibits ATP synthesis and metabolism. This indicated that both Pyr and BaP entered the cells by the same means of passive transport. Biodegradation of Pyr and BaP did not differ in the early stage of culture, but around days 5–7, the biodegradation efficiency of BaP was significantly (30–61%) higher than that of Pyr. Key enzymes involved in these processes were identified and their activity differed, with intracellular gentisate 1,2-dioxygenase and extracellular polyphenol oxidase as likely candidates to be involved in BaP degradation, while intracellular catechol-1,2- dioxygenase and salicylate hydroxylase are more likely involved in Pyr degradation. These results provide new insights for sustainable environmental remediation of pyrene and benzo(a)pyrene by these bacteria.

Effect of Normalization Methods on Accuracy of Estimating Low- and High-Molecular Weight PAHs Distribution in the Soils of a Coking Plant

Mapping spatial distribution of soil contaminants at contaminated sites is the basis of risk assessment. Hotspots can cause strongly skewed distribution of the raw contaminant concentrations in soil, and consequently can require suitable normalization prior to interpolation. In this study, three normalization methods including normal score, Johnson, and Box-Cox transformation were performed on the concentrations of two low-molecular weight (LMW) PAHs (i.e., acenaphthene (Ace) and naphthalene (Nap)) and two high-molecular weight (HMW) PAHs (i.e., benzo(a)pyrene (BaP) and benzo(b)fluoranthene (BbF)) in soils of a typical coking plant in North China. The estimating accuracy of soil LMW and HMW PAHs distribution using ordinary kriging with different normalization methods was compared. The results showed that all transformed data passed the Kolmogorov-Smirnov test, indicating that all three data transformation methods achieved normality of raw data. Compared to Box-Cox-ordinary kriging, normal score-, and Johnson-ordinary kriging had higher estimating accuracy of the four soil PAHs distribution. In cross-validation, smaller root-mean-square error (RMSE) and mean error (ME) values were observed for normal score-ordinary kriging for both LMW and HMW PAHs compared to Johnson- and Box-Cox-ordinary kriging. Thus, normal score transformation is suitable for alleviating the impact of hotspots on estimating accuracy of the four selected soil PAHs distribution at this coking plant. The findings can provide insights into reducing uncertainty in spatial interpolation at PAHs-contaminated sites.

Comparison of polycyclic aromatic hydrocarbon accumulation in crab tissues with the ambient marine particles from shallow hydrothermal vents, northeast Taiwan

This study investigated and compared polycyclic aromatic hydrocarbons (PAHs) in crab (Xenograpsus testudinatus), suspended particulate matter, and surface sediment sampled from Kuei-shan-tao (KST) shallow water vents just offshore northeast Taiwan. The total concentrations of PAHs (t-PAHs) in suspended particles near the vents (533–685 ng g−1 dw) were two orders of magnitude higher than the overlying sediment (3.42–6.06 ng g−1 dw). The t-PAHs in sediment were significantly lower than those found in suspended particulate matter and all crab tissues tested, including hepatopancreas (192–1154 ng g−1 dw), gill (221–748 ng g−1 dw), muscle (30–174 ng g−1 dw), and exoskeleton (22–96 ng g−1 dw). Principal component analysis (PCA) indicated tissue-specific bioaccumulation of PAHs in crabs. The compositions of PAHs in gill, muscle, and exoskeleton were mainly low molecular weight, while the composition in the hepatopancreas included both high and low molecular weight PAHs. Highly variable but characteristic PAH congeners and concentrations in crab tissues and ambient aquatic particles reflect bioaccumulation.

Considering zooplankton as a black box in determining PAH concentrations could result in misjudging their bioaccumulation

Zooplankton play an important role in energy transfer in the marine food web and form the dietary basis for the size of important fish stocks and the maintenance of their resources. Although zooplankton include numerous taxa with significantly different ecological characteristics and the interspecific differences in optimum body size and taxonomic specificity in fish feeding on zooplankton are remarkable, they are always considered as a whole (like a “black box”) in current studies about the transport of persistent organic pollutants through the food chain. This approach might result in misjudgment of their bioaccumulation. In this study, the distribution properties of each taxa of zooplankton community were discerned using data from two cruise surveys conducted in the northern South China Sea. Twelve groups of zooplankton were identified, all of which had distinct ecological and functional characteristics. The carbon-based community structure of zooplankton could explain their variability with respect to polycyclic aromatic hydrocarbons (PAHs). Smaller-sized zooplankton (smaller calanoids and cyclopoids) were more likely to accumulate low molecular weight PAHs (LMW-PAHs), while larger-sized zooplankton (larger calanoids) were more likely to accumulate high molecular weight PAHs (HMW-PAHs). The bioaccumulation capacity of the zooplankton community for LMW-PAHs was negatively correlated with the proportion of omnivores and carnivores, while the opposite was true for HMW-PAHs. These results suggested that the effects of complex community structure within plankton communities should be taken into account when assessing the transfer and bioaccumulation effects of PAHs in the marine food chain.

Temporal and spatial pattern of dust storms, their polycyclic aromatic hydrocarbons, and human health risk assessment in the dustiest region of the world.

This study evaluated the concentration and health risks of polycyclic aromatic hydrocarbons (PAHs) in Abadan City under 4 different climatic conditions: normal days, dusty days, dust with northwesterly winds, and dust with southeasterly winds. It also determined the sources of aromatics and discussed the relationship between meteorological parameters and PAH concentrations. The spatiotemporal distribution of dust in the area was determined using the HYSPLIT (hybrid single-particle Lagrangian integrated trajectory) back trajectory model, moderate resolution imaging spectroradiometer (MODIS) images. For this purpose, sampling was performed for 70days using an Omni device. The concentrations of 16 PAHs (USEPA) ranged from 46.22 to 90.96ng/m3. The highest concentration of high molecular weight (HMW) PAHs was 4-6 rings, of which 4 rings were predominant in all samples. PAH sources were identified using diagnostic ratios and principal component analysis (PCA), and it was shown that PAHs mainly originate from a mixture of sources, including vehicular emissions, petrol emissions, and traffic. Wind speed was negatively correlated with dust, except on dusty days. This result indicates a decrease in PAH concentrations when wind speed increases. On the other hand, the dust correlation with PAH was positive on normal days, but a negative correlation was observed on dusty days. This result was due to the lower concentration of PAHs from natural resources (such as dust source areas) vs. human resources (such as traffic and industry). PAH health risk assessment in Abadan City showed that the risk of carcinogenesis was higher on normal days and through skin contact. The probability of incremental lifetime cancer risk (ILCR) in all sampling conditions was potential in terms of carcinogenic risk (10-4-10-6). As a critical risk factor, relevant authorities should prevent, control, and reduce it.

Degradation of pyrene in sediments based on the activation of peroxymonosulfate with nitrogen-doped magnetic biochar: Synergistic effect and mechanism

Pyrene (PYR) is a typical high molecular weight polycyclic aromatic hydrocarbon (HMW-PAH) with potential biotoxicity and resistance to biodegradation, and the accumulation of PYR in sediments increases the risk to ecosystems. Therefore, this study evaluated the catalytic performance of nitrogen-doped magnetic biochar-activated peroxymonosulfate system (NMBC/PMS) on PYR in sediments and elucidated its mechanism. The results showed that the degradation rate of PYR in sediments by the NMBC/PMS system reached 87% at PMS= 1 × 10−4 M, NMBC= 3.0 g/L and pH= 9, which conformed to the pseudo-first-order rate law, and the rate constant(Kobs) was 7.3 × 10−2 h−1. The high adsorption performance of NMBC was attributed to π-π electron donor-acceptor interactions (π-π EDA). The high degradation performance of NMBC/PMS system was attributed to the active sites generated by graphitization, magnetism, and electronegativity of NMBC, which were the key to activate PMS to degrade PYR. The results of X-ray photoelectron spectroscopy (XPS), quenching experiments and electron paramagnetic resonance (EPR) analysis indicated that N-doping and Fe3O4-loading on NMBC synergistically promoted the degradation of PYR. In addition, the mechanism of PYR degradation by NMBC/PMS system was investigated, indicating that SO4·-, HO·and 1O2 were the main reactive oxygen species. The excellent recoverability of NMBC showed its application potential. The NMBC/PMS system developed in this study provided a theoretical basis for a future multi-pathway synergistic degradation mechanism of PYR in sediments.

Bioaccumulation of polycyclic aromatic hydrocarbons (PAH) in Polychaeta Marphysa sanguinea in the anthropogenically impacted Tunis Lagoon: DNA damage and immune biomarkers.

This work assessed the impact of polycyclic aromatic hydrocarbons (PAHs) on the polychaeta Marphysa sanguinea in Tunis Lagoon. Highest PAHs concentrations were accumulated at station E with maximum Σ PAH of 6028,87ng/g DW. Changes in animal physiology were clearly related to bioaccumulated PAH. In fact, high levels of immune biomarkers (cyclooxygenase [COX] and lysozyme activity with maximum of 44631,10 FU/mn/mg protein and 0,017 lysozyme activity/mn/mg protein, respectively) were recorded at stations B and E. Triacylglycerol (TAG), the energy source, was lowest at the most polluted stations (E and B), while phospholipids (PL) were highest at the control station. Statistical analysis revealed a probable effect of both low and high molecular weight PAHs on variations in energy storage lipids (TAG and sterol and wax esters [SE/WE]) and membrane lipids, particularly PL. Our results encourage the use of M. sanguinea to assess pollution levels in coastal ecosystems.

Peculiar polycyclic aromatic hydrocarbons accumulation patterns in a non-zooxanthellate scleractinian coral.

Assessing the sources and accumulation patterns of polycyclic aromatic hydrocarbons (PAHs) in corals is critical, as they threaten coral ecosystem resilience in addition to other anthropogenic pressures. We determined acenaphthene, fluorene, fluoranthene, and pyrene concentration in the skeleton and soft tissue of 7 adult and 29 old specimens of the non-zooxanthellate coral Leptopsammia pruvoti from the Mediterranean Sea. Leptopsammia pruvoti accumulated 2–72 times higher PAH concentrations than the previously investigated zooxanthellate Balanophyllia europaea living at the same site at shallower depth, likely in relation to the different trophic strategy. Low molecular weight PAHs were preferentially accumulated compared to high molecular weight PAHs. Detected PAHs were mainly petrogenic, consistently with local pollution sources. Populations of L. pruvoti immobilized PAHs in the skeleton 3–4 orders of magnitude more efficiently than B. europaea . This highlights the need to investigate other non-zooxanthellate species, which represent the majority of Mediterranean scleractinians, but are widely overlooked with respect to the few zooxanthellate species. • Coral trophic strategy influences PAH accumulation patterns in skeleton and tissue. • Low molecular weight PAHs were preferentially accumulated. • Populations of heterotrophic corals store PAH in the skeletons very efficiently.

Benzo[A]Pyrene and Benzo[E]Pyrene: Photoreactivity and Phototoxicity toward Human Keratinocytes.

Polycyclic aromatic hydrocarbons (PAHs) are a group of organic compounds derived mostly from the incomplete combustion of fossil fuels and biomass. Human skin can absorb PAHs and the uptake increases with their molar mass and lipophilicity. Benzopyrene is high molecular weight PAH frequently appearing in ambient pollution. It exists in two isomeric forms: benzo[a]pyrene (BaP) and benzo[e]pyrene (BeP), which exhibit different biological activity. Although certain properties of benzopyrenes suggested photoreactivity of the compounds, no direct measurements were previously conducted to characterize their photochemical activity. In this study, quantum yield and action spectra of singlet oxygen photogeneration by BaP and BeP were measured by time-resolved near-infrared phosphorescence, and the ability of both compounds to photogenerate superoxide anion was assessed by electron paramagnetic resonance (EPR) spin-trapping. The measurements revealed high efficiency of benzopyrenes to photogenerate singlet oxygen and their ability to photogenerate superoxide anion. Using HaCaT cells as single-layer skin model, we demonstrated concentration-dependent and light-dependent cytotoxicity of BaP and BeP. The compounds induced damage to the cell mitochondria and elevated the levels of intracellular reactive oxygen species.

Health Risks Associated with Polycyclic Aromatic Hydrocarbons (PAHs) in Dustfall Collected from Universities in Wuhan, China

Atmospheric dustfall samples from the libraries and dormitories of 14 universities in Wuhan, China, were collected and analyzed for 16 priority polycyclic aromatic hydrocarbons (PAHs). The results showed that the levels of Σ16PAHs in the dustfall from libraries varied from 2.45 to 13.4 μg·g−1, with an average value of 5.06 μg·g−1, while that of dormitories ranged from 2.61 to 10.6 μg·g−1, with an average of 5.19 μg·g−1. The compositions of PAHs in library and dormitory dustfall were similar, and they were dominated by high molecular weight PAHs (HMW-PAHs) (including fluoranthene, benzo(b)fluoranthene, and chrysene), which accounted for 79.2% of the total PAHs. Spatially, the higher levels of PAHs contamination were mainly distributed in areas with high population density and heavy traffic, which suggests that anthropogenic activities made an important contribution to the PAHs emissions. The diagnostic ratios and principal component analyses (PCA) indicated that combustion-related anthropogenic sources, such as petroleum, coal, and biomass combustion, as well as vehicular traffic emission, were the main sources of PAHs bound to dustfall. The toxic equivalent concentrations (BaPeq) of dustfall-bound PAHs ranged from 271 to 2510 μg·kg−1. According to the health risk assessment results, dermal contact was the predominant exposure pathway, followed by ingestion and inhalation. The incremental lifetime cancer risks (ILCRs) of exposure to PAHs in dustfall was 1.230 × 10−6−1.140 × 10−5, which indicates that there are low potential carcinogenic risks in the universities.

MOLECULAR CHARACTERISATION OF BACTERIA MONOOXYGENASE AND DEHYDROGENASE GENES INVOLVED IN PAHs REMEDIATION

Bacterial catabolic genes (alkB, alkH, C12O, and C23O) are a good biomarker for choosing the choice of the organism for polycyclic aromatic hydrocarbon (PAH) degradation. Low molecular weight (LMW) and high molecular weight (HMW) PAHs metabolism can be made possible by monooxygenase and dehydrogenase enzymes which code for the catabolic genes. In this study, the monooxygenase and dehydrogenase genes were characterized from the bacterial population isolated from motor mechanic workshop soils and landfill soil artificially polluted with waste engine oil (WEO). Standard microbiological methods were followed for the isolation and characterization of the bacterial population. The PCR cycling for alkB and alkH followed initial denaturation at 94oC for 5 minutes, followed by 35 cycles of denaturation at 95oC for 1 minute, annealing at the correct temperature (alkB 49oC, alkH 72oC). PCR cycling for C12O and C23O genes followed initial denaturation at 95oC for 5 minutes, 35 cycles of denaturation at 94oC for 20 s, annealing at 63oC for 30 s, extension at 60oC for 45 s, with final extension for 5 minutes at 72oC. Final elongation step for all the catabolic genes at 72oC for 10 minutes and holding temperature at 10oC forever. Amplified fragments were visualized on safe view-stained 1.5% agarose gel electrophoresis. The result of the characterization revealed base pair sizes of the genes; alkB (100 to 300 bp), alkH (< 700 bp), C12O (>250 bp), and C23O (<80 pb). All the bacterial populations invested in this study expressed the monooxygenase and dehydrogenase genes. Monooxygenase and dehydrogenase genes are coding for the enzymes responsible for hydroxylation and intradiol or extradiol ring-cleaving of PAHs.

Mixed polyaromatic hydrocarbon degradation by halotolerant bacterial strains from marine environment and its metabolic pathway

Accidents involving diesel oil spills are prevalent in sea- and coastal regions. Polycyclic aromatic hydrocarbons (PAHs) can be adsorbed in soil and constitute a persistent contaminant due to their poor water solubility and complex breakdown. PAHs pollution is a pervasive environmental concern that poses serious risks to human life and ecosystems. Thus, it is the need of the hour to degrade and decontaminate the toxic pollutant to save the environment. Among all the available techniques, microbial degradation of the PAHs is proving to be greatly beneficial and effective. Bioremediation overcomes the drawbacks of most physicochemical procedures by eliminating numerous organic pollutants at a lower cost in ambient circumstances and has therefore become a prominent remedial option for pollutant removal, including PAHs. In the present study, we have studied the degradation of Low molecular Weight and High Molecular Weight PAH in combination by bacterial strains isolated from a marine environment. Optimum pH, temperature, carbon, and nitrogen sources, NaCl concentrations were found for efficient degradation using the isolated bacterial strains. At 250 mg/L concentration of the PAH mixture an 89.5% degradation was observed. Vibrio algiolytcus strains were found to be potent halotolerant bacteria to degrade complex PAH into less toxic simple molecules. GC-MS and FTIR data were used to probe the pathway of degradation of PAH.

Transcriptome responses in copepods Calanus finmarchicus, Calanus glacialis and Calanus hyperboreus exposed to phenanthrene and benzo[a]pyrene.

Arctic and sub-arctic pelagic organisms can be exposed to effluents and spills from offshore petroleum-related activities and thus it is important to understand how they respond to crude oil related contaminants such as polycyclic aromatic hydrocarbons (PAHs). The copepod species Calanus finmarchicus, Calanus glacialis and Calanus hyperboreus represent key links in the arctic marine food web. We performed a transcriptome analysis of the three species exposed to phenanthrene (Phe) and benzo[a]pyrene (BaP) representing low and high molecular weight PAHs, respectively. Differential expression of several genes involved in many cellular pathways was observed after 72h exposure to Phe (0.1μM) and BaP (0.1μM). In C. finmarchicus and C. glacialis, the exposure resulted in up-regulation of genes encoding enzymes in xenobiotic biotransformation, particularly the phase II cytosolic sulfonation system that include 3'-phosphoadenosine 5'-phosphosulfate synthase (PAPSS) and sulfotransferases (SULTs). The sulfonation pathway genes were more strongly induced by BaP than Phe in C. finmarchicus and C. glacialis but were not affected in C. hyperboreus. However, a larger number of genes and pathways were modulated in C. hyperboreus by the PAHs including genes encoding xenobiotic biotransformation and lipid metabolism enzymes, suggesting stronger responses in this species. The results suggest that the cytosolic sulfonation is a major phase II conjugation pathway for PAHs in C. finmarchicus and C. glacialis. Some of the biotransformation systems affected are known to be involved in metabolism of endogenous compounds such as ecdysteroids, which may suggest potential interference with physiological and developmental processes of the copepod species.

Spatial Distribution, Potential Sources, and Health Risk of Polycyclic Aromatic Hydrocarbons (PAHs) in the Surface Soils under Different Land-Use Covers of Shanxi Province, North China.

Polycyclic aromatic hydrocarbons (PAHs) are widespread in the environment and pose a serious threat to the soil ecosystem. In order to better understand the health risks for residents exposed to PAH-contaminated soil, 173 surface soil samples were collected in Shanxi Province, China, to detect the levels of 16 priority PAHs. The spatial distribution patterns of PAHs were explored using interpolation and spatial clustering analysis, and the probable sources of soil PAHs were identified for different land-use covers. The results indicate that the soil Σ16 PAH concentration ranged from 22.12 to 1337.82 ng g−1, with a mean of 224.21 ng g−1. The soils were weakly to moderately contaminated by high molecular weight PAHs (3–5 ring) and the Taiyuan–Linfen Basin was the most polluted areas. In addition, the concentration of soil PAHs on construction land was higher than that on other land-use covers. Key sources of soil PAHs were related to industrial activities dominated by coal burning, coking, and heavy traffic. Based on the exposure risk assessment of PAHs, more than 10% of the area was revealed to be likely to suffer from high carcinogenic risks for children. The study maps the high-risk distribution of soil PAHs in Shanxi Province and provides PAH pollution reduction strategies for policy makers to prevent adverse health risks to residents.