Sources Of Polycyclic Aromatic Hydrocarbons Contamination Research Articles

Accumulation and Toxicity of Polycyclic Aromatic Hydrocarbons in Long-Term Soil Irrigated with Treated Wastewater

Our study focuses on examining the effects of treated wastewater irrigation (TWWI) on agricultural soils in water-scarce regions, with a specific emphasis on the presence and accumulation of polycyclic aromatic hydrocarbons (PAHs). This issue is particularly significant due to its potential threats to environmental security. During our research, we discovered the existence of 16 different PAHs in these soils, which are known to have harmful impacts on ecosystems and human health. The concentration of total PAHs ranged from 163.9 ng g−1 to 9177.4 ng g−1, with 4- and 5-ring PAHs being the most dominant contributors. The PAHs Fluoranthene and Pyrene were found to be the most prevalent in all soil samples. Comparing the PAH concentrations in our research area to those reported in other studies, we observed that the agricultural areas in our study were more contaminated. Through positive matrix factorization (PMF) and diagnostic ratios (DRs) analyses, we identified petroleum combustion, vehicular emissions, as well as coal, grass, or wood combustion as the primary sources of PAH contamination. We also noted a negative correlation between clay, silt, pH, and PAH concentrations, while a significant positive relationship was observed between total organic carbon (TOC), sand, and PAHs. Based on the computed environmental risk index value, the presence of PAHs in the area poses a moderate to high level of ecological risk. TWWI was identified as the main contributor to PAHs in the agricultural soils we studied. Therefore, it is crucial to establish and enforce standards for wastewater reuse in agricultural fields before irrigation takes place.

Spatial and individual factors mediate the tissue burden of polycyclic aromatic hydrocarbons in adult and chick brown pelicans in the northern Gulf of Mexico

The northern Gulf of Mexico supports a substantial level of oil and gas extraction in marine waters and experiences acute and chronic exposure to marine pollution events. The region also supports a diverse array of breeding and migratory seabirds that are exposed to these pollutants during foraging and other activities. Among the pollutants of highest concern within the region are polycyclic aromatic hydrocarbons (PAHs) which tend to be toxic, carcinogenic, mutagenic, or teratogenic. We assessed PAH loads in blood from adult brown pelicans and from feathers of adults and chicks of brown pelicans in relation to individual (e.g., body condition, sex) and spatial (e.g., breeding location within the Gulf, home range size, migration distance) factors. Of the 24 PAHs assessed, 17 occurred at least once among all samples. There were no PAHs found in chicks that were not also found in adults. Alkylated PAHs occurred more commonly and were measured at higher summed concentrations compared to parent PAHs in all samples, indicating that exposure to oil and/or byproducts of oil may have been a substantial source of PAH contamination for brown pelicans during this study. Within adults, PAHs were more likely to occur, and to increase in concentration, in blood samples of females compared to males, although no difference was found in feather samples. We also found that occurrence of and concentration of PAHs increased in adults that migrated longer distances. In adults and chicks, the background levels of oil and gas development within the region of the colony was not a consistent predictor of the presence of or concentration of PAHs. We also found correlations of PAHs with hematological and biochemical biomarkers that suggested compromised health. Our results indicate that both short- and long-term exposure (i.e., blood and feathers, respectively) are occurring for this species and that even nest-bound chicks can accumulate high levels of PAHs. Long-term tracking of PAHs, as well as an assessment of sublethal effects of PAHs on pelicans, could enhance our understanding of the persistence and effects of this contaminant in the northern Gulf as could increasing the breadth of species studied.

Analysis on Contamination Characteristics, Pollution Source Identification and Ecological Risk Assessment of Polycyclic Aromatic Hydrocarbons of Groundwater in a Large Coking Plant Site of Province

Polycyclic aromatic hydrocarbons (PAHs), as a highly toxic persistent organic pollutant, are commonly found in soil and water environments. In recent years, the pollution of PAHs in groundwater has attracted wide attention from scientists. To study the pollution characteristics and sources of polycyclic aromatic hydrocarbon in groundwater of the coking site, 16 PAHs priorly controlled by the US EPA were analyzed and discussed. In this study, we identified the contamination characteristics of PAHs in groundwater, analyzed the pollution sources of PAHs, and evaluated the ecological risk of PAHs in the coking site by combining statistical techniques, the positive matrix factorization (PMF) model, and risk quotient (RQ) methods. The results indicated that the total detection rate of PAHs in groundwater of the coking plant was 46.7%. The concentrations of PAHs in groundwater of the coking plant ranged from below the detection limit to 444.9 μg·L-1, with the average value of 1.88 μg·L-1. The concentration of PAHs in the groundwater of different production workshops was significantly different. The most polluted workshop was in the tar-refining area, and the concentration of 16 PAHs was 444.9 μg·L-1. Based on the PMF model, we identified the two primary contamination sources of PAHs in groundwater of the coking plant:① oil combustion and ② coal and biomass combustion and oil leakage. The contribution ratios of the two sources to PAHs of groundwater were 38.6% and 61.4%, respectively. The results of the ecological risk assessment indicated that Σ16PAHs in groundwater of the coking plant had high ecological risk, and the ecological risk of single PAHs in 53.4% of the groundwater sampling site was at a high ecological risk level. In conclusion, it is urgent to carry out the treatment and restoration of the groundwater environment in the coking plant site.

Exposure and Risk Assessment of Korean Firefighters to PBDEs and PAHs via Fire Vehicle Dust and Personal Protective Equipment.

In this study, the levels of polycyclic aromatic hydrocarbons (PAHs) and polybrominated diphenyl ethers (PBDEs) were characterized in firefighters' personal protective equipment (PPE) (i.e., jackets, pants, hoods, and gloves) and vehicle dust wipe samples to assess the exposure and potential risk of firefighters to these combustion-related toxic pollutants. The mean levels of ∑PBDEs in the fire vehicle dust samples (778 and 449 pg/cm2 for pump trucks and command cars, respectively) were significantly higher than those in the private vehicles (31.2 pg/cm2) (Kruskal-Wallis test, p < 0.05), which was similar to the ∑PAH levels (521, 185, and 46.8 pg/cm2 for pump trucks, command cars, and private vehicles, respectively). In the case of firefighters' PPE, the levels of ∑PBDEs and ∑PAHs in used jackets and pants were found to be, respectively, 70- to 2242-folds and 11- to 265-folds higher than those in their unused counterparts. Biomass/petroleum combustion was found to be the main source of PAH contamination in fire vehicle dust and used PPE in the present study. Both carcinogenic and noncarcinogenic risks via vehicle dust ingestion and dermal absorption from wearing of PPE were within permissible limits, although the relative risk evaluation showed that PAH/PBDE absorption via wearing of PPE could pose a higher likelihood of carcinogenic and noncarcinogenic risks than the ingestion of pollutants via fire vehicle dust, warranting the need for appropriate management of firefighters' personal protective ensembles.

Toxicity determination, pollution source delineation, and microbial diversity evaluation of PAHs-contaminated sediments for an urban river.

The Feng-Sang River is a metropolitan river in Kaohsiung City, Taiwan. In this study, Feng-Sang River sediments were analyzed to investigate the distributions and sources of polycyclic aromatic hydrocarbons (PAHs). The Sediment Quality Guidelines (SQGs), potentially carcinogenic PAHs (TEQcarc), and toxic equivalence quotient (TEQ) were applied to evaluate influences of PAHs on ecosystems and microbial diversities. Results indicate that PAHs concentrations varied between seasons and locations. The concentrations of ∑16PAHs ranged from 73.6 to 603.8 ng/kg in dry seasons and from 2.3 to 199.3 ng/kg in wet seasons. This could be because of the flushing effect during wet seasons, which caused the movement and dilution of the PAH-contaminated sediments. Diagnostic ratio analysis infers that high PAHs levels were generated by combustion processes and vehicle traffic, and results from multivariate descriptive statistical analysis also demonstrate that the vehicular traffic pollution could be the major emission source of PAHs contamination. Comparisons of PAHs with SQGs indicate that PAHs concentrations in sediment were below the effects range low (ERL) values, and thus, the immediate threat to organisms might not be significant. The diagnostic ratio analyses are effective methods for PAH source appointment. The metagenomic assay results imply that sediments contained essential microbial species with eminent diversity. The detected PAH-degrading bacteria (Desulfatiglans, Dechloromonas, Sphingomonas, Methylobacterium, Rhodobacter, Clostridium, and Exiguobacterium) played a key role in PAHs biotransformation, and Dechloromonas and Rhodobacter had a higher relative abundance. Results of microbial diversity analyses indicate that the contaminated environment induced the changes of governing microbial groups in sediments. PRACTITIONER POINTS: Diagnostic ratio analyses are effective methods for PAHs source appointment. Microbial composition in sediments are highly affected by anthropogenic pollution. Combustion and vehicle traffic contribute to urban river sediments pollution by PAHs. Dechloromonas and Rhodobacter are dominant PAHs-degrading bacteria in sediments.

Phase partitioning effects on seasonal compositions and distributions of terrigenous polycyclic aromatic hydrocarbons along the South China Sea and East China Sea

Polycyclic aromatic hydrocarbons (PAHs) have posed serious risk to marine ecosystems due to their carcinogenic properties, and persistence in the environment and elevated bioaccumulation. It, therefore, becomes essential to examine spatial distribution, composition, and sources of PAHs. In this study, we have examined these PAH variations in the South China Sea (SCS) and East China Sea (ECS), that are experiencing rapid population and economic growth by the surrounding developing countries. It revealed high seasonal variations that significantly differ between dissolved and particulate PAHs concentrations. Spatial variations of PAHs across sites remain relatively insignificant. Persistently high particulate concentrations of the Naphthalene (Nap) were observed, whereas the dissolved concentrations of Fluorene (Flu) and Phenanthrene (Phen) remained prevalent across all the seasons. The result of non-metric multidimensional scaling (NMDS) strongly reflects the weak dispersions of PAHs across the seasons and the contrasting effects of the phase partitioning. Principal component analysis indicates that the primary source of PAH contamination is coal tar or petroleum distillation. However, estimated risk quotient (RQ) values of both the dissolved and particulate PAHs in all the seasons are far below the high-risk levels, while dissolved PAHs displayed relatively higher values. This study signifies the importance of phase petitioning for PAHs monitoring and potential risk assessments.

Distribution, risk assessment, and source apportionment of polycyclic aromatic hydrocarbons (PAHs) using positive matrix factorization (PMF) in urban soils of East India.

This study investigated 16 United States environmental protection agency priority PAHs profiles and their sources in 40 urban soils collected from two industrialised cities, Jamshedpur and Bokaro, in east India and assessed their health risk to humans. The results showed the predominance of high molecular weight (HMW) PAHs (4-5 rings). The total PAHs concentration in surface soils ranged from 2223 to 11,266ng/g and 729 to 5359ng/g (dw), respectively, for Jamshedpur and Bokaro. Higher concentrations of PAHs were recorded at the selected industrial areas and heavy traffic zones of both cities. In JSR city 4-ring PAHs contributed 43% of total PAHs trailed by 5-ring PAHs 27.2%. Similarly, in BKR city 4-ring PAHs contributed 34% of the total PAHs, followed by 3-ring PAHs 28.9% and 5-ring PAHs 22.9%. Total organic carbon in surface soils exhibited moderate correlation with the low molecular weight (ΣLMW) PAHs (R2 = 0.69) and a comparatively strong correlation with the ΣHMW PAHs (R2 = 0.89), suggesting strong adsorption of HMW PAHs to urban soils. The Diagnostic and PMF modelling analysis indicated that the major sources of PAHs contamination in soils were petroleum combustion, vehicular emissions, biomass, and coal combustion. The health risk assessment shows that the cumulative probability of carcinogenic risks was under the acceptable limits of 10-4 to 10-6. At some sampling areas in both cities, the maximum value of total exposure cancer risk slightly exceeded the acceptable limits indicating some carcinogenic risk for adults.

Determination of Polycyclic Aromatic Hydrocarbons in Batman River by Liquid-liquid and Solid-phase Extractions and the Statistical Comparison of the Two Extraction Techniques

Polycyclic Aromatic Hydrocarbons (PAHs), which have detrimental health effects such as cancer and mutation, abound in rivers. To employ effective mitigation strategies, accurate determination of PAHs in water bodies is essential. In this study, PAHs in the Batman River were investigated. Specifically, the study has two aims: (1) determining whether there are any statistical differences between the Liquid-liquid (LL) and Solid-phase (SP) extraction techniques of PAHs; and (2) investigation of PAH contamination and the potential sources of PAHs in the Batman River. Methodologically, four different samples were collected and one part of each sample was extracted with the LL and the other part with the SP. Later, each extract was analyzed using gas chromatography-mass spectrometry. Subsequently, the analysis results of the LL and SP extracts were statistically compared. PAH concentrations were 85.5 and 76.7 ng/L for the means of the LL and SP extracts, respectively. Based on the t-test, the differences between these two means were not significant (p-value=0.684 &amp;gt; 0.05). Similarly, no statistical differences were observed between the analysis results of the LL and SP extracts for any individual PAHs. As for the source analysis, the results indicated that road vehicles and coal combustion were the possible sources of PAH contamination in the river. This study provides the first data set for PAH contamination in the Batman River.

Evaluation of silicone-based wristbands as passive sampling systems using PAHs as an exposure proxy for carcinogen monitoring in firefighters: Evidence from the firefighter cancer initiative

Compared to the general population, firefighters are known to sustain greater levels of exposure to hazardous compounds, despite their personal protective equipment, also known as turnout gear. Among the most significant toxins that firefighters are chronically exposed to are polycyclic aromatic hydrocarbons (PAHs). Additionally, firefighters have also been noted to exhibit an increased incidence of certain types of cancer. Considering a probable link between exposure to PAHs and increased rates of cancer in the fire service, we aim to document ambient chemical concentrations in the firefighter work environment. Our strategy involves the use of silicone-based wristbands that have the capacity to passively sorb PAHs. To determine if wristbands can serve as an effective chemical monitoring device for the fire service, silicone wristbands were pilot-tested as personal sampling devices for work environment risk monitoring in active-duty firefighters. Recovered wristbands underwent multiple extraction steps, followed by GC-MS analysis to demonstrate their efficacy in monitoring PAHs in the firefighter environment. Initial findings from all wristband samples taken from firefighters showed multiple exposures to various PAHs of concern for the health of the firefighters when in a fire environment. In addition to PAH monitoring, we examined known and potential sources of PAH contamination in their work environment. To that end, profiles of elevated PAH concentrations were documented at various fire stations throughout South Florida, for individual firefighters both during station duties and active fire response.

Assessment of polycyclic aromatic hydrocarbon contamination in the Sundarbans, the world’s largest tidal mangrove forest and indigenous microbial mixed biofilm-based removal of the contaminants

The distribution of polycyclic aromatic hydrocarbons (PAHs) in the surface water and sediments in five regions of the Indian Sundarbans was assessed. The capability of microbial biofilm communities to sequester PAHs in a biofilm-promoting vessel was evaluated. The total PAH concentration of water and sediments ranged from undetectable to 125 ng ml−1 and 4880 to 2 × 104 ng g−1 dry weight respectively. The total PAHs concentration of sediments exceeded the Effects Range–Low value and the recommended Effects Range-Median values, implying the PAHs might adversely affect the biota of the Sundarbans. Pyrogenic and petrogenic sources of PAH contamination were identified in most of the sampling sites. Indigenous biofilms were cultivated in a patented biofilm-promoting culture vessel containing liquid media spiked with 16 priority PAHs. Biofilm-mediated 97–100% removal efficiency of 16 PAHs was attained in all media. There was no significant difference between the mean residual PAH from the liquid media collected from hydrophobic and hydrophilic flasks. Residual amounts of acenaphthene (Ace), anthracene (Ant), benzo(b)fluoranthene [B(b)F], benzo(a)pyrene [B(a)P] and benzo(g,h,i)perylene [B(g,h,i)P] showed differences when cultivated in hydrophobic and hydrophilic flasks. The mean residual amounts of total PAHs extracted from biofilm biomasses were variable. A biofilm obtained from a specific sampling site cultured in the hydrophobic flask showed higher PAH sequestration when compared to the removal attained in the hydrophilic flask. Relative abundances of different microbial communities in PAH-sequestering biofilms revealed bacterial phyla including Proteobacteria, Bacteroidetes, Firmicutes, Actinobacteria, Chloroflexi and Planctomycetes as well as members of Ascomycota phylum of fungi. The dominance of Candida tropicalis, Clostridium butyricum, Sphingobacterium multivorum and Paecilomyces fulvus were established.

Forest fires as potential triggers for production and mobilization of polycyclic aromatic hydrocarbons to the terrestrial ecosystem

AbstractAlthough forest fires have been identified as an important source of polycyclic aromatic hydrocarbons (PAHs), this problematic has not been thoroughly studied yet. This study addressed the role of wildfires and time since fire in the production and mobilization of PAHs to the terrestrial compartment. Levels of 15 priority PAHs were assessed in topsoil and ash samples (by GC–MS analysis) collected in two burnt areas and an unburnt one, comprising two types of vegetation coverage and four sampling occasions after fire. The fire had triggered an immediately increase of PAH levels in topsoil, according to the comparison of burnt and unburnt samples, but this impact had largely faded 4 months later. Although the fire severity did not play a role in immediate postfire PAH contents in topsoil and ashes, variations were found with the type of vegetation coverage being higher in pine slopes. The wildfire event markedly changed PAHs composition through enrichment in three‐ring PAHs (69% vs. 27%, burnt and unburnt, respectively), which dwindled more markedly in topsoil than in ashes. This study pointed out the key role of wildfires as a source of PAHs to the terrestrial compartment, as unveiled by the increased levels in topsoil and ashes. Additionally, it was found that PAHs could be mobilized from these matrixes over the first year after the fire, possibly leading to aquatic contamination. This finding suggests wildfires as a diffuse source of PAH contamination to freshwater systems, which need to be considering in future monitoring/management programs on the environmental impact of wildfires.

Benzo(a)Pyrene Equivalency and Source Identification of Priority Polycyclic Aromatic Hydrocarbons in Surface Sediments from Yamuna River

ABSTRACTIdentification of polycyclic aromatic hydrocarbons (PAHs) sources in the environmental compartments is crucial, but there is a need for appropriate management and remediation plan in the environment. PAHs can provide useful information, because they have been utilized for source apportionment. In this study, priority 16 PAHs were determined in sediments from Yamuna River in Delhi for the assessment of their possible sources. Among 16 PAHs, the dominant compounds were fluoranthene, chrysene, fluorine, and pyrene, and their sum accounted for more than 96% of the total 16 priority PAHs. The concentrations of ∑16PAHs at locations between upstream and downstream were not showing any considerable spatial gradient. The concentration of seven probable carcinogenic PAHs ranged 236–6230 µg kg−1 with the mean value of 1897 ± 1740 µg kg−1, and accounted for 40% of the ∑16PAHs. Benzo(a)pyrene toxic equivalent factors (TEFs) used for the quantification of relative toxicity potential of priority PAHs in terms of BaP toxicity equivalency (BaPTEQ) were presented. Homolog profiles demonstrated the dominance of two-, three-, and four-ring PAHs. Composition profile and selected concentration ratios of PAHs were used as diagnostic tools for the identification of possible emission sources of PAHs. The study suggested the pyrogenic activities of petroleum, coal, and biomass combustions as a major source of PAH contamination in the river. However, marginally petrogenic sources from automobile workshops and accidental spillage cannot be ruled out. The observed levels of total PAHs and their toxicity equivalency in sediments were more or less comparable with similar studies carried out worldwide.

Polycyclic aromatic hydrocarbons in house dust and surface soil in major urban regions of Nepal: Implication on source apportionment and toxicological effect

Urban centers have turned to be the provincial store for resource consumptions and source releases of different types of semi-volatile organic compounds (SVOCs) including polycyclic aromatic hydrocarbons (PAHs), bringing about boundless environmental pollutions, among different issues. Human prosperity inside urban communities is unambiguously dependent on the status of urban soils and house dusts. However, environmental occurrence and sources of release of these SVOCs are challenging in Nepalese cities, as exceptionally very limited data are accessible. This motivated us to explore the environmental fate, their source/sink susceptibilities and health risk associated with PAHs. In this study, we investigated the contamination level, environmental fate and sources/sink of 16 EPA's priority pollutants in surface soil and house dusts from four major cities of Nepal. Additionally, the toxicological effect of individual PAH was studied to assess the health risk of PAHs. Generally, the concentrations of ∑16PAHs in surface soil were 1.5 times higher than house dust, and ranged 767–6770ng/g dry weight (dw) (median 1810ng/g dw), and 747–4910 dw (median 1320ng/g dw), respectively. High molecular weight-PAHs both in soil and dust were more abundant than low molecular weight-PAHs, suggesting the dominance of pyrogenic source. Moderate to weak correlation of TOC and BC with PAHs in soil and dust suggested little or no role of soil organic carbon in sorption of PAHs. Source diagnostic ratio and principal component analysis indicated fossil fuel combustion, traffic/vehicular emissions and combustion of biomass are the principal sources of PAHs contamination in Nepalese urban environment. The high average TEQ value of PAHs in soil than dust suggested high risk of soil carcinogenicity compared to dust.

Polycyclic aromatic hydrocarbons (PAHs) in sediment and sea urchin (Echinometra mathaei) from the intertidal ecosystem of the northern Persian Gulf: Distribution, sources, and bioavailability

The distribution, sources and bioavailability of polycyclic aromatic hydrocarbons (PAHs) in sediment and sea urchin (Echinometra mathaei) from the intertidal zone of the northern Persian Gulf were investigated. Total PAH concentrations varied from 12.8 to 81.25 and from 16.7 to 35 μgKg−1 dry weight in sediment and Echinometra mathaei, respectively. The PAH concentrations can be classified as low. Source identification and apportionment using diagnostic ratios and principal component analysis demonstrate that the combustion of fossil fuels, road traffic, combustion of natural gas and biomass, and oil spill could be considered as the main sources of PAH contamination. The first PAH biota-sediment accumulation factors (BSAF) data from sediment to Echinometra mathaei in the intertidal zone of the northern Persian Gulf were calculated, indicating accumulation of both lower and higher molecular weight PAHs, with a preferential accumulation of lower molecular weight PAHs.

Novel photochemical advanced oxidation process for the removal of polycyclic aromatic hydrocarbons from polluted concrete

Polycyclic aromatic hydrocarbons (PAHs) are denoted by International Agency for Research on Cancer as mutagens, teratogens and carcinogenic to humans. In 2013, Vinča Institute of Nuclear Sciences was hired to determine whether PAHs are present in significant quantities in the concrete walls of newly built residential buildings (about 15,000m2 of apartments), and to propose appropriate technical solution for PAH removal in this case. As PAH occurrence, determination and remediation in concrete is, to our knowledge, a completely new field, it was necessary to face a number of challenges, including lack of regulations considering contents of PAHs in concrete, investigation of the origin of PAH contamination in concrete (if established), as well as finding feasible and non-expensive remediation method, which would be appropriate for residential space. In first part of this study, a markedly high concentrations of 5PAHs were detected by UPLC/PDA analysis in samples of both concrete walls and mineral oil used for coating of planks during formwork, while control concrete and mineral oil, taken from independent construction site, were taken as a reference. Such coincidence, as well as the fact that mineral oil has penetrated into the concrete which is proven by ASAP/MS analysis, pointed to the mineral oil as the most probable source of PAH contamination of the concrete. In the second part, an efficient and easy-applicable method for PAH oxidation in concrete (called FHO3AOP), using UV light, H2O2 and ozone, was presented and discussed in terms of previous literature data.

Spatial-temporal distributions, sources of polycyclic aromatic hydrocarbons (PAHs) in surface water and suspended particular matter from the upper reach of Huaihe River, China

The spatial and temporal distribution of polycyclic aromatic hydrocarbons (PAHs) in surface water from the upper reach of Huaihe River were investigated. The water and suspended particulate matter (SPM) samples from 16 sites were collected during three sampling cruises. The concentrations of ΣPAHs ranged from 79.94 to 421.07ng/L with the average values of 140.37ng/L in water and from 10.87 to 201.42ng/L with the average values of 61.23ng/L in SPM. In comparison to survey during March 2007, alleviated PAHs pollution was ascribed to the adjustment of energy structure. LMW PAHs (2- and 3-ring) were abundant in water and SPM samples with high detection frequencies. Seasonal variations of PAHs indicated that high concentrations of PAHs were recorded in the dry period (67.47–560.16ng/L) and low levels of PAHs were detected in the flood period (27.87–458.47ng/L) in water, while the high concentration of PAHs in SPM ranged from 4.14 to 342.32ng/L in the dry period and low concentration from 2.42 to 129.23ng/L in the level period. In situ water-SPM phase distribution revealed that PAHs tended to be transported with water phase in the studied area. Ratios of specific PAHs were calculated to evaluate the possible sources of PAHs contamination, which reflected PAHs in water and SPM derived from the mixed of pyrogenic and petroleum origins in different seasons.

Tracking human footprints in Antarctica through passive sampling of polycyclic aromatic hydrocarbons in inland lakes

Freely dissolved polycyclic aromatic hydrocarbons (PAHs) were monitored in seven inland lakes of Antarctica by a polyethylene (PE)-based passive sampling technique, with the objective of tracking human footprints. The measured concentrations of PAHs were in the range of 14–360 ng L−1 with the highest values concentrated around the Russian Progress II Station, indicating the significance of human activities to the loading of PAHs in Antarctica. The concentrations of PAHs in the inland lakes were in the upper part of the PAHs levels in aquatic environments from remote and background regions across the globe. The composition profiles of PAHs indicated that PAHs in the inland lakes were derived mainly from local oil spills, which was corroborated by a large number of fuel spillage reports from ship and plane crash incidents in Antarctica during recent years. Clearly, local human activities, rather than long-range transport, are the dominant sources of PAH contamination to the inland lakes. Finally, the present study demonstrates the efficacy of PE-based passive samplers for investigating PAHs in the aquatic environment of Antarctica under complex field conditions.

Sources appointment and ecological risk assessment of polycyclic aromatic hydrocarbons (PAHs) in sediments of Erhai Lake, a low-latitude and high-altitude lake in southwest China.

Sixteen polycyclic aromatic hydrocarbons (PAHs) were analyzed from the surficial sediments in Erhai Lake, a plateau lake in China. The results showed that except for acenaphthylene (Ace) Ace and Dibenz(a,h)anthracene (DBA), the central region contained individual PAHs at concentrations lower than those in other lake regions. Total concentration of the PAHs (ΣPAHs) in the sediments from Erhai Lake ranged from 32.42 to 558.53 mg/kg with a mean value of 256.70 mg/kg. The maximum value of ΣPAHs was observed in the north region of the lake and more than 10-fold higher than the minimum values. Moreover, high molecular weight (HMW) PAHs, especially 5-ring PAHs, accounted for higher ratios up to 76 % relative to other PAHs compound in almost all sampling sites. Molecular diagnostic ratios including anthtacene (Ant)/(Ant + phenanthrene (Phe)), fluoranthene (Flt)/(Flt + pyrene (Pyr)), benz(a)anthracene (BaA)/(BaA + chrysene (Chr)), and indeno(1,2,3-cd)pyrene (IPY)/(IPY + benz(g,h,i)perylene (BPE)) were recorded at all sampling sites and indicated that the origin of PAHs in Erhai Lake was predominately pyrolytic. Furthermore, principal component analysis with component dominating by HMW PAHs showed that combustion origins were the primary contamination sources of PAHs in the sediments of Erhai Lake. Finally, ecological risk assessment indicated that the sediments from Erhai Lake are exposed to potential low risk for ΣPAHs, and the ecological risk decreases in the order of northern region > southern region > central region.

국내 토지이용도별 토양 중 다환방향족탄화수소류(PAHs)의 농도 수준 및 분포 특성

We investigated soil contamination depending on the land use by examining the contamination levels and distribution characteristics of 16 polycyclic aromatic hydrocarbons (PAHs) in the national soil. Total PAHs (the sum of 16 PAH concentrations) and carcinogenic PAHs (the sum of seven carcinogenic PAH concentrations) were 8.50~3,437.16 µg/kg and 2.94~2,136.96 µg/kg, respectively. The concentration of benzo(a)pyrene, one of the contaminants regulated by the soil quality standard in the nation, was ND~924.73 µg/kg. Its maximum value of 924.73 µg/kg was detected in railroad (Region 3) and is approximately 13% of the standard value for Region 3 (i.e., 7 mg/kg). We also investigated the characteristics of contamination sources of PAHs in soil of the upland, forests, roads, and railroads, examining the fraction distribution of PAHs concentration by the number of benzene rings against the total PAHs concentration. The results demonstrate that the mean fraction of 4~6-ring PAHs against total PAHs concentration in soil was in the range of 51.8~80.7% with relative abundance of high-molecular PAHs, showing that the origin of contamination is under the category of combustion sources. When the molecular indices (Flu/(Flu/Pyr), Ant/(Ant+Phe), InP/(InP+BP), and BaA/ (BaA+Chr)) were applied, they were also categorized as petroleum-based combustion sources. The individual PAH concentrations in soil by the land use were grouped into Regions 1, 2, and 3, which are statistically treated and are the parts of the national category system of soil quality standard. As a result, the concentration level of 16 PAHs was 0.02~2.63 µg/kg in Region 1, 0.05~4.26 µg/kg in Region 2, and 2.36~178.27 µg/kg in Region 3. The concentration level of 6 carcinogenic PAHs was 14.2~320.4% against that of benzo(a)pyrene in Region 3 and sites of recycling waste sleepers. Considering that there were similarities among PAHs in terms of structures and toxicities, it would be recommended to review other types of carcinogenic PAHs together with benzo(a)pyrene when developing the soil quality standards in the nation.

Microsatellite DNA mutations in double-crested cormorants (Phalacrocorax auritus) associated with exposure to PAH-containing industrial air pollution.

Hamilton Harbour, Ontario, Canada is one of the most polluted sites on the Great Lakes, and is subject to substantial airborne pollution due to emissions from both heavy industry and intense vehicle traffic. Mutagenic Polycyclic aromatic hydrocarbons (PAHs) are present at very high concentrations in the air and sediment of Hamilton Harbour. We used five variable DNA microsatellites to screen for mutations in 97 families of Double-crested Cormorants (Phalacrocorax auritus) from three wild colonies, two in Hamilton Harbour and one in cleaner northeastern Lake Erie. Mutations were identified in all five microsatellites at low frequencies, with the majority of mutations found in chicks from the Hamilton Harbour site closest to industrial sources of PAH contamination. Microsatellite mutation rates were 6-fold higher at the Hamilton Harbour site closest to the industrial sources of PAH contamination than the other Hamilton Harbour site, and both were higher than the reference colony. A Phase I metabolite of the PAH benzo[a]pyrene identified by LC-MS/MS in bile and liver from Hamilton Harbour cormorant chicks suggests that these cormorants are exposed to and metabolizing PAHs, highlighting their potential to have caused the observed mutations.