USEPA Priority Polycyclic Aromatic Hydrocarbons Research Articles

Air–plant interaction and air–soil exchange of polycyclic aromatic hydrocarbons in a large human-influenced reservoir in southwest China

The Three Gorges Reservoir (TGR) is totally manmade, strongly influenced by anthropogenic activity, and lies on the upper reaches of Yangtze River. The periodic storage and discharge of water from the Three Gorges Dam could have altered the original air-plant/soil interactions of contaminants in TGR. Herein, paired atmospheric gas–particle, air–plant, and air–soil samples were collected to investigate the air–plant interaction and air–soil exchange of 16 USEPA priority polycyclic aromatic hydrocarbons (PAHs). The air–plant interaction based on McLachlan's framework to our datasets suggests that PAHs were absorbed via gaseous deposition that was restricted by the plant–gas dynamic equilibrium. The equilibrium indicates a dynamic balance between the gaseous phase and plant surface in PAH absorption. The main limiting factor influencing the PAH uptake was the plant species rather than the atmospheric PAH concentration. The air–soil exchange of PAHs exhibited a net volatilization flux of 16.71 ng/m2/d from the soil to the air based on annual average. There was more volatilization and less deposition in summer and more deposition and less volatilization in autumn and winter. The soil serves as a secondary source of atmospheric PAHs. As the first attempt on probing the multi-interface geochemical process of PAHs, this study highlights the influence of manual water level manipulation from the TGD and environmental factors (such as temperature, humidity, and soil properties) on the regional fate of PAHs in the TGR.

Source identification of polycyclic aromatic hydrocarbons (PAHs) in soils around crude oil contaminated area in Ohaji/Egbema, Imo State

ABSTRACT This study aims to determine the source of polycyclic aromatic hydrocarbons (PAHs) in the soils surrounding an area in Ohaji/Egbema, Imo State, that has been contaminated by crude oil. Soil samples were collected in the study area using a soil auger at a depth of 0–20 cm at three sampling locations (sample A, sample B, and sample C) in the Mmahu community in Ohaji/Egbema. In each of the sampling locations, twenty sub-samples were collected from twenty sampling points and pooled together to form representative samples for each of the sampling locations. Prior to GC-MS analysis, the composite samples were air-dried, sieved through a 2-mm mesh, and then kept in pet bottles that had been previously cleaned. The GC-MS investigations were carried out using a Shimadzu Model 2010 GC-MS (Shimadzu, Japan) fitted with an HP-5 MS fused silica column. This was used to quantify the 16 USEPA priority PAHs in the studied soils. The sum of the 16 USEPA priority PAHs in the sample locations ranged from 0.0192 mg/kg in the control sample to 10.73 mg/kg in sample A. Compared to high molecular weight PAHs (4–6 rings), the total concentration of low molecular weight PAHs (2–3 rings) was found to be substantially greater. According to the PAH molecular diagnostic ratio, all sampling points had low to high molecular mass ratios >1, which suggests that the origin of the PAH contamination was petrogenic. The petrogenic source of contamination was attributed to oil spillage around the study area. The knowledge of source identification of PAHs in soils helps in the determination of the most appropriate remediation strategy in order to prevent further contamination and minimise the risks to human health and the environment.

Concentration of Polycyclic Aromatic Hydrocarbons in Water from Hand-dug Wells in Some Communities in Ekpeyeland, Rivers State, Nigeria

Well water sources from selected communities in Ekpeyeland were assessed for the concentrations of polycyclic aromatic hydrocarbons (PAHs). The assessment was conducted seasonally in six communities. The concentrations of the PAHs were determined using standard methods and procedures and finally quantified by the use of GC-MS chromatography. The result showed the presence of all the 16 USEPA priority PAHs in the examined water samples. Seasonal variations were not significant. The summed values of PAHs from stations and seasons were above the permissible limit required for by WHO. Classification of the different categories of PAHs identified higher molecular weight (HMW) PAHs more in concentration than lower molecular weight (LMW) PAHs in the wells. Source identification proved that both pyrogenic and petrogenic sources were responsible for the presence of PAHs in the well water. However, pyrogenic source was the more prominent source of PAHs in the water. There was high level of carcinogenic PAHs in the water and thus the water portends danger to the users. Therefore, the locals are advised not to consume the water to avoid its effect on the long run.

Chemical characterization, source identification and potential health effects of PM2.5-bound non-polar organic compounds over a COALESCE network site - Bhopal, India

Year-long (2019) measurements of carbonaceous aerosols were performed at Bhopal, a regionally representative site as a part of the COALESCE (Carbonaceous Aerosol Emissions, Source apportionment and Climate Impacts) campaign. Aerosol-associated non-polar organic compounds (NPOCs) were analysed using thermal desorption (TD) Gas chromatography/Mass spectrometry (TD-GC/MS). The annual average of the total organic carbon (OC), elemental carbon (EC), and analysed PAHs (Polycyclic Aromatic Hydrocarbons), and n-alkanes were, 9.74 ± 9.47 μg m−3, 2.13 ± 3.12 μg m−3, 10.43 ± 5.49 ng m−3, and 114.93 ± 49.24 ng m−3, respectively. PAHs diagnostic ratios suggested emissions from petroleum, grass, wood, and coal combustion. Combustion derived PAHs (CombPAHs) accounted for 72.5 % of the total measured PAHs. During wintertime, based on Pyr/BaP ratio (∼0.6), gasoline exhaust emissions were higher compared to diesel exhaust emissions. The weak correlations between PAHs and meteorological parameters suggested that variations in PAH levels are primarily driven by alterations in emission sources. Total PAHs were correlated moderately with BrC (r2 = 0.60). The estimated lifetime lung cancer risk (LLCR) values on exposure to 16 USEPA priority PAHs (5 × 10−5) demonstrated that PAH levels in this region pose moderate health risks. Given observations from only campaign mode short-term measurements of NPOCs over India, this work provides a more comprehensive understanding of the concentrations, seasonal variations, and sources of n-alkanes and health risk associated with particle bound PAHs over the data-poor central Indian region.

Removal of PAHs in paddy fields: How natural periphytic biofilm enhances the removal process and the mechanisms involved

Previous studies on the removal of polycyclic aromatic hydrocarbons (PAHs) from farmland have mostly relied on anthropogenic biotic or abiotic amendments. Here, an indigenous paddy periphytic biofilm (PB) composed of complex symbolic communities was enriched, and its essential role, as well as the potential mechanisms of PAHs dissipation, was investigated. A pot experiment revealed that PB achieved 92.87% and 92.76% removal of the USEPA priority PAHs from the overlying water and soil of a heavily PAHs-contaminated paddy field, respectively. This subsequently decreased ΣPAHs accumulation in rice shoots to 4.12 ± 1.08 ng g-1, under the thresholds based on food safety standards. The physiology of PB in an aquatic culture with PAHs was assessed to understand the toxicity and removal mechanism. Extracellular polymeric substances (EPS) adsorption occurred in the early stage, followed by late biodegradation, which was considered the primary mechanism for removing PAHs. In this process, the PB contributed more to the high molecular weight PAHs compared to the low molecular weight. Furthermore, 16S-rRNA sequencing demonstrated specific functional phyla (Proteobacteria, Ascomycota, and Chloroplastida) with significantly higher relative abundances in periphytic communities with PAHs, which facilitated PAHs degradation. The predicted synergetic metabolic pathway involved 33 PAHs-degrading genes as inferred by PICRUSt. These findings suggest that PB could provide a promising strategy for target PAHs remediation in situ and food safety in contaminated paddy fields.

Probing the occurrence, sources and cancer risk assessment of polycyclic aromatic hydrocarbons in PM2.5 in a humid metropolitan city in China.

Fifty-two consecutive PM2.5 samples from December 2021 to February 2022 (the whole winter) were collected in the center of Chongqing, a humid metropolitan city in China. These samples were analysed for the 16 USEPA priority polycyclic aromatic hydrocarbons (16 PAHs) to explore their composition and sources, and to assess their cancer risks to humans. The total concentrations of the 16 PAHs (ng m-3) ranged from 16.45 to 174.15, with an average of 59.35 ± 21.45. Positive matrix factorization (PMF) indicated that traffic emissions were the major source (42.4%), followed by coal combustion/industrial emission (31.3%) and petroleum leakage/evaporation (26.3%). The contribution from traffic emission to the 16 PAHs increased from 40.0% in the non-episode days to as high as 46.2% in the air quality episode during the sampling period. The population attributable fraction (PAF) indicates that when the unit relative risk (URR) is 4.49, the number of lung cancer cases per million individuals under PAH exposure is 27 for adults and 38 for seniors, respectively. It was 5 for adults and 7 for seniors, when the URR is 1.3. The average incremental lifetime cancer risk (ILCR) for children, adolescents, adults and seniors was 0.25 × 10-6, 0.23 × 10-6, 0.71 × 10-6, and 1.26 × 10-6, respectively. The results of these two models complemented each other well, and both implied acceptable PAH exposure levels. Individual genetic susceptibility and exposure time were identified as the most sensitive parameters. The selection and use of parameters in risk assessment should be further deepened in subsequent studies to enhance the reliability of the assessment results.

Toxicological Risk Evaluation of Polycyclic Aromatic Hydrocarbons in Soils from a Petroleum Spillage Site at Kokori in the Niger Delta Region of Nigeria

Polycyclic aromatic hydrocarbons (PAHs) are widespread environmental contaminants that are produced by the incomplete combustion of organic sources and are widely found in soils. This present research was carried out to evaluate the concentrations and toxicological risk assessment of the United States Environmental Protection Agency's sixteen priority polycyclic aromatic hydrocarbons (16 priority PAHs) in soils from the vicinity of an oil spillage site in Delta State of Nigeria. The level of pollution and potential toxicological health hazards of the PAHs were assessed in surface soil samples using soxhlet extraction of and Gas Chromatography-Mass Spectrometry (GC-MS). Thirteen out of the sixteen USEPA priority PAHs were detected in the soil sample. The concentrations of PAHs in the petroleum-contaminated soils in this investigation ranged from 0.01181 ppm to 1.16054 ppm, with the total estimated concentration of the 16 priority PAHs being 5.6713 ppm. Furthermore, the distribution of the PAHs in the study area was predominated by LMW PAHs (62%) over HMW PAHs (38%). Additionally, the total toxicity equivalency quotients TEQ (B[a]Peq) result of the carcinogenic potency of the USEPA priority PAHs was calculated as 0.08689 ppm (8.689%) and was discovered to be within the Canadian TEQ (B[a]Peq) threshold of 0.6 ppm. This suggests that the soil in the study area is safe based on the Canadian TEQ (B[a]Peq) standard and does not constitute a carcinogenic risk. However, the long-term bioaccumulation of these low quantities of PAHs in human has been found to constitute a potential health concern due to bioaccumulation in living systems.

Physicochemical and Polycyclic Aromatic Hydrocarbons (PAHs) Analysis in Soil and Sediment from Vicinity of Ikot Akpaden, Akwa Ibom State, Nigeria

The study was undertaken to determine the levels of 16 priority PAHs in soil and sediments from some vicinities of Ikot Akpaden, Mkpat Enin. The soils were prepared using standard procedure in the laboratory and analyzed for 16 US EPA priority PAHs using Gas Chromatography-Mass Spectrophotometer (GC-MS). The soil samples were obtained from two sampling sites at Ikot Akpaden (Site A and C). Site C showed minimal PAHs concentration while site A recorded PAHs levels ranging from 0.01 to 4.25 mg/kg. According to European commission, the PAHs concentrations in soil samples of this study are moderate, but deleterious over time. The soils were negatively affected more with low molecular weight PAHs than High Molecular Weight PAHs.This study revealed that the sampling sites had low carcinogenic burden, hence would exhibit moderate adverse health effects to plants and animals. It was concluded that automobile repair activities in site A contributed to the soil contamination with PAHs; hence it should be properly sited.

Assessment of various conditions for the simultaneous determination of US EPA and EU priority PAHs in coffee samples and their PAHs consumption risk

The optimal conditions for simultaneous determination of the U.S. Environmental Protection Agency (US EPA) and European Union (EU) priority polycyclic aromatic hydrocarbons (PAHs) in coffee beans and coffee brews were developed. The QuEChERS (quick, easy, cheap, effective, rugged and safe) technology combined with high performance liquid chromatography - temperature-controlled fluorescence detection and gas chromatography - tandem mass spectrometry were used in the investigation. PAHs could be determined in commercially available green coffee beans (possibly caused by environmental contamination), and their PAHs content increased with the degree of roasting. Coffee beans brewed with the coffee machine released more PAHs into their brews than those brewed with the drip bag. The PAHs consumption risk of the brewed coffee samples was not high due to their low PAH level. Nevertheless, the methods of roasting and brewing and the amount of drinking could still be considered to reduce the intake of PAHs.

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

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

In situ investigation of N deposit effects on polycyclic aromatic hydrocarbons (PAHs) photolysis in snow

As snow is an ideal scavenger of polycyclic aromatic hydrocarbons (PAHs) for both particulate- and gas-phase PAHs, a large amount of PAHs are accumulated in snowpacks. These PAHs could be released from seasonal snowpacks into environment over a short time during the snow melting period, causing a flush of contaminants. Understanding the fate of PAHs in snow therefore is important to evaluate the contaminant flush during snow melting. However, as an important natural process, PAH photolysis in snow is still unclear, especially in the context of global climate change. Therefore, photolysis of the 16 PAHs, which are listed as priority controlled pollutants by United States Environmental Protection Agency (US EPA), was investigated with N deposit in field in snow in this study. A mixture of the 16 US EPA priority PAHs and nitrate/ammonia were spiked into sealed quartzose bottles containing snow samples in field. The bottles were then exposed to solar radiation in field for 6 h. Experimental results showed that >50% of PAHs were lost during 6 h photolysis, mostly occurred in the first hour. Generally, HMW PAHs were photolyzed faster than LMW PAHs, though the photolysis rate did not strictly increase with molecular weight. Low concentrations of nitrate can enhance photolysis of Ant and Pyr, while photolysis of investigated PAHs was inhibited with nitrate concentration increasing. In contrast, both low and high concentration of ammonium can inhibit PAH photolysis. The inhibiting effect of both nitrate and ammonia on photolysis of HMW PAH is stronger than that of LMW PAHs, indicating direct photolysis of PAHs is the main pathway of PAH degradation in snow in situ. This study firstly showed the effect of N deposition on PAH photolysis in snow. Under current increasing N deposition in northeast China, this study implied that more PAHs in snow could be preserved during winter and released shortly during snowmelt, resulting in high ecological risk in spring.

Emission factors for polycyclic aromatic hydrocarbons from laboratory biomass-burning and their chemical transformations during aging in an oxidation flow reactor

Atmospheric polycyclic aromatic hydrocarbons (PAHs) can be emitted from different combustion sources including domestic biomass burning, internal combustion engines, and biomass burning (BB) in wild, prescribed, and agricultural fires. With climate warming and consequent global increases in frequency and severity of wildfires, BB is a dominant source of PAHs emitted into the atmosphere.In this study, six globally and regionally important and representative fuels (Alaskan peat, Moscow peat, Pskov peat, eucalyptus, Malaysian peat, and Malaysian agricultural peat) were burned under controlled conditions in the combustion chamber facility at the Desert Research Institute (DRI, Reno, NV, USA). Gas- and particle-phase BB emissions were aged in an oxidation flow reactor (OFR) to mimic five to sevendays of atmospheric aging. To sample gas- and particle-phase BB emissions, fresh and OFR-aged biomass-burning aerosols were collected on Teflon-impregnated glass fiber filters (TIGF) in tandem with XAD resin media for organic carbon speciation. The objectives of this study were to i) quantify the emission factors for 113 PAHs emitted from the combustion of the six selected fuels, ii) characterize the distribution of PAH compounds between gas and particle phases for these fuels, iii) identify the changes in PAHs during OFR-aging, and iv) evaluate toxicity potential with characterized compounds.We found that combustion emissions of gas-phase PAHs were more abundant (>80 % by mass) than particle-phase PAHs, for emissions from all combusted fuels. The mass fraction of substituted napthalenes in Moscow peat and Malaysian peat emissions were ∼70 % & 84 %, respectively, whereas in Eucalyptus the same fraction was <50 %, which indicates that these substituted compounds can be used as tracers for peat emissions. Mass concentrations of gas- and particle-phase PAHs were reduced by ∼70 % after OFR oxidation. However, the understanding of the fate of PAHs during OFR oxidation requires further investigations. Our results also indicate that the PAH toxicity of BB samples would be underestimated by 10–100 times if only the BaPeq for the 16 US EPA priority PAHs in the particle phase are included.

The recalcitrance and potential toxicity of polycyclic aromatic hydrocarbons within crude oil residues in beach sediments at the BIOS site, nearly forty years later

The Arctic is a unique environment characterized by extreme conditions, including daylight patterns, sea ice cover, and some of the lowest temperatures on Earth. Such characteristics in tandem present challenges when extrapolating information from oil spill research within warmer, more temperate regions. Consequently, oil spill studies must be conducted within the Arctic to yield accurate and reliable results. Sites of the Baffin Island Oil Spill (BIOS) project (Cape Hatt, Baffin Island, Canadian Arctic) were revisited nearly 40 years after the original oil application to provide long-term monitoring data for Arctic oil spill research. Surface and subsurface sediment samples were collected from the intertidal zone of the 1981 nearshore oil spill experiment (Bay 11), from 1980 supratidal control plots (Crude Oil Point) and 1982 supratidal treatment plots (Bay 106). Samples were analyzed for Polycyclic Aromatic Hydrocarbons (PAHs) and alkylated homologues via Gas Chromatography – Mass Spectrometry (GC-MS). Our results suggest that total mean concentrations of all measured PAHs range from 0.049 to 14 mg/kg, whereas total mean concentrations of the 16 US EPA priority PAHs range from 0.02 to 2.1 mg/kg. The relative proportions of individual PAHs were compared between sampling sites and with the original technical mixture. Where available, percent loss of individual PAHs was compared with data from samples collected at the BIOS site, in 2001. All three sites featured samples where concentrations of various priority PAHs exceeded the established Interim Marine Sediment Quality Guidelines. All supratidal samples contained potentially toxic levels of PAHs. Even after nearly four decades of weathering, the recalcitrant crude oil residues remain a potential hazard for the native organisms. Continued monitoring of this unique study site is crucial for establishing a timeline for oil degradation, and to observe a reduction in toxicity over time.

Study on the variations of extractable polycyclic aromatic hydrocarbons in lignite and semi-coke

Low-temperature pyrolysis is one of the most important technologies for the clean and efficient utilization of lignite. Semi-coke, the solid product of this process, has been widely used as both an industrial and household clean fuel. In this study, three lignites from China (EE), Indonesia (YN), and Mongolia (WM) and their semi-cokes obtained through pyrolysis at 550 °C were treated with dichloromethane, and the extracted polycyclic aromatic hydrocarbons (PAHs) were analyzed using a gas chromatograph/mass spectrometer. The results showed that the total concentrations of PAHs in EE, YN, and WM were 125000, 4400, and 5800 ng/g, respectively, and those in their semi-cokes were 4700, 10000, and 5500 ng/g, respectively. The concentrations of alkylated PAHs (aPAHs) were higher than those of parent 16 US EPA priority PAHs (16 PAHs) in lignites, while parent 16 PAHs were more abundant in semi-cokes. Both lignites and semi-cokes were dominated by 2-ring PAHs (naphthalene and alkylated naphthalenes), followed by 3- and 4-ring PAHs. The proportion of 2-ring PAHs in the semi-cokes increased with respect to that in the lignites, and the degree of alkylation of the PAHs decreased. This suggested that the extractable PAHs changed to smaller parent PAHs during the low-temperature pyrolysis. The concentration and composition of PAHs in the mobile phase of the semi-coke are an important part of its structural characteristics and are closely related to the macromolecular structure of raw coal. Thus, this study on PAHs in semi-coke provides relevant information on the structural evolution of coal during pyrolysis and further improves our understanding of clean fuel.

Polycyclic aromatic hydrocarbons (PAHs) in surface soils of tropical reef islands in China under external plant and soil introduction: Occurrence, sources, risks, and relationships with soil properties, vegetation cover, and soil source

This study explored the levels, sources, and risks of PAHs in soils from Yongle Atoll (YLA) and Xuande Atoll (XDA) of the Xisha Islands (XSIs) in the South China Sea, China, under different vegetation cover types and soil sources. The results clearly showed that the levels of 16 US EPA priority PAHs (Σ16PAHs) are relatively low in XDA and YLA, with concentrations ranging from not detected (ND) to 151 ng/g (average 15.7 ng/g) and ND to 5.8 ng/g (average 2.1 ng/g), respectively. Three- and four-ring PAHs (62.3% and 53.8%) were widely distributed in YLA and XDA. The average concentration of Σ16PAHs in soils with shrub cover was 1.4, 1.8, 4.8, and 5.0 times higher than that in soils with herbaceous cover, vegetable cover, arbor cover, and no plant cover, respectively. Source analysis using binary diagnostic ratios and the positive matrix factorization (PMF) model suggested that PAHs have similar sources (gasoline/coal combustion, coke production, and biomass combustion), but different contributions in native soil and introduced soil. Moreover, diesel-related vehicular emission was identified to be an additional source of PAHs in native soil. Pearson's correlations revealed strong relationships between PAHs and organic matter or total organic carbon. The cancer risk of PAHs varied among different vegetation cover types and soil sources, following the orders herbaceous cover > vegetable cover > shrub cover > arbor cover > no plant cover and introduced soil > mixed soil > native soil. Nevertheless, the risk remained lower than the risk threshold (10−6), suggesting low carcinogenesis risk in the two atolls. Our findings provide new evidence for the introduction of external vegetation/soil acting as a driver of changes in the characteristics of PAHs in islands, and also underline the negligibility of the PAH increase in soils in the South China Sea, China, from the perspective of health hazards.

Characterization, source apportionment, and risk assessment of polycyclic aromatic hydrocarbons (PAHs) in urban soils from 23 cities in China.

Concentrations, composition profiles, sources, and health risks of 16 USEPA priority polycyclic aromatic hydrocarbons (PAHs) in urban soils from 23 cities across China based on metadata collected from previous studies between 2005 and 2021 were investigated. ΣPAH concentrations in urban soils from 23 cities across China ranged from 0.1231 to 17.2000mg/kg (mean = 2.7171 ± 3.8276mg/kg). Overall PAH contamination in urban soils across China was moderate compared to that in global cities. Based on energy consumption and climate conditions, the spatial distributions of mean ΣPAH concentrations in Northeast China were highest, followed by those in North China, West China, East China, and South China. Individual PAH composition profiles decreased in the order: 4-ring PAHs (41.36%) > 5-ring PAHs (21.77%) > 3-ring PAHs (18.53%) > 6-ring PAHs (14.00%) > 2-ring PAHs (2.27%). Diagnostic ratios and positive matrix factorization (PMF) revealed that PAHs in urban soils were mainly derived from fossil fuel combustion (from coal, natural gas, and biomass), especially in North, Northeast, and East China, with smaller contributions from petrogenic sources. Health risk assessment results suggest that although there are potential cancer risks from PAHs, risks were acceptable. Toxic equivalent concentration (TEQ) and the corresponding oral cancer slope factor (CFS0) contributed most to the uncertainty of total risks. This study will help develop strategies to reduce PAH risk management in urban soils in China.

New insight into human health risk from polycyclic aromatic hydrocarbons on surfaces of buildings and facilities for industrial legacy regeneration

Although many industrial heritage sites have been repurposed into attractive landscapes, the contamination and health risks from polycyclic aromatic hydrocarbons (PAHs) on industrial legacy surfaces remain unexplored. We collected 441wiping surface samples from 95 buildings and facilities at Beijing coking plant in China and found that the concentrations of 16 US EPA priority PAHs (∑16PAHs) ranged from ND-982.16 and ND-4262.20 mg/m2 on the surfaces of buildings and facilities, respectively. The main source of PAHs was the coking process, and spatial distribution of PAHs was consistent with ∑16PAHs in the soil. The carcinogenic risks of BaP, DBA, BbF, BaA, Ind of the facilities remained as industrial heritage relics, and those of Bap, DBA and BbF in the buildings with commercial uses exceeded the acceptable level (10−6). The hazard quotient of 9 PAHs was below the acceptable level (1.0). The remedial goals for BaP and DBA (0.11 mg/m2) and BbF, BaA and Ind (1.14 mg/m2) at the facility heritage relics were derived. Similarly, the RGs for the buildings with commercial uses of BaP, DBA and BbF were 0.16, 0.16, and 1.64 mg/m2, respectively. Overall, we determined that carcinogenic PAHs on the surfaces of industrial legacy should be regulated for regeneration.

Polycyclic aromatic hydrocarbons in selected rivers in southwestern Nigeria: Seasonal distribution, source apportionment and potential risk assessment

The river sediment has been identified as major potential threats to ecosystem and human health due to its repository ability towards pollutants including polycyclic aromatic hydrocarbons (PAHs). A total of 72 surface sediment samples from six major rivers within south-western Nigeria were collected during both wet and dry seasons. Sixteen USEPA priority PAHs were analyzed using GC–MS for profile composition, potential sources, and ecological and human health risks on seasonal basis. PAHs were detected in all analyzed sediments at varying concentrations: ∑16 PAHs ranging from 1226 to 13,093 μg/kg (mean: 1356–12,850 μg/kg) and 1495 to 13,845 μg/kg (mean: 1536–13,671 μg/kg) across all locations during the dry and wet seasons respectively. However, the spread of PAH differs from each location. The carcinogenic PAHs (∑PAH7C) dominated the high molecular weight (HMW) PAH profile (≥ 97%) and accounting for 28 to 45% of the Σ16PAHs, presenting a high carcinogenic potential. Elevated Σ PAHs and ΣPAH7C were observed during the wet season. The study observed varied benzo(a) pyrene (BaP eq) equivalent concentrations across the rivers, suggesting variability in carcinogenic potency. Six-ring PAHs constituted the least composition in all the rivers (< 0.08–0.53 μg/kg) while three and four-ringed PAHs dominated the composition profile. Carbonaceous materials such as black carbon and particulate organic carbon notably influenced PAHs distribution (R2≥0.733, p < 0.05 ). Results of diagnostic ratios suggested the predominance contributions of coal and biomass combustion to PAHs distributions over petrogenic sources by positive matrix factorization (PMF). Further studies on the levels of PAHs in edible seafood transportation processes of PAHs is recommended for developing appropriate risk analysis approaches.

Differential accumulation of polycyclic aromatic hydrocarbons (PAHs) in three earthworm ecotypes: Implications for exposure assessment on historically contaminated soils

This study compared accumulation of the 16 US-EPA priority polycyclic aromatic hydrocarbons (PAHs) in three different earthworm ecotypes, Amynthas sp., Eisenia fetida, and Lumbricus terrestris, in four historically (> 50 years) contaminated manufactured gas plant (MGP) soils using bioassays. Epi-endogeic deep burrowing and soil ingesting Amynthas sp. accumulated significantly more ∑16 PAHs than any other species (upto 8.7 times more), and epigeic surface dwelling E. fetida showed the lowest ∑16 PAH accumulation. Results indicated the importance of earthworm habit and physiology on PAH partitioning into earthworm lipids. Exposure to soil borne PAHs via the gut, as compared with passive diffusion from pore water, was important in species tested, being most evident in burrowing species Amynthas sp. and L. terrestris and for the desorption-resistant higher molecular weight (HMW) PAHs. Biota-soil accumulation factors (BSAF) were low, as influenced by aging, sequestration and strong PAH sorption to secondary sorptive phases in the historically contaminated soils. Bioconcentration factors (BCFs) calculated from freely dissolved pore water PAH concentrations derived from polyoxymethylene solid-phase extractions (POM) were species specific, indicating stronger relationships with octanol-water partition coefficient (KOW) for Amynthas sp. and L. terrestris than for E. fetida. Modelling demonstrated that KOW values were not a reliable proxy for BCF in equilibrium partitioning theory (EqPT) to predict bioavailability for the range of earthworms tested, being less accurate for E. fetida compared to the burrowing species. The study showed that including burrowing and soil feeding earthworm species, such as Amynthas sp. and L. terrestris, in standard testing would benefit regulatory decisions for more accurate quantification of PAH bioavailability in ecological risk assessment on historically contaminated soils.

Sources, Toxicity, Health and Ecological Risks of Polycyclic Aromatic Hydrocarbons (PAHs) in the Sediment of an Osogbo Tourist River

ABSTRACT This study investigated twenty-three polycyclic aromatic hydrocarbons (PAHs) in the sediment of Osun River, spanning through both the peri-urban and urban areas of the river, to estimating their sources, ecological and health hazards. The sampling locations covered those beside major roads and agricultural farms. They were analyzed by gas chromatography-mass spectrometry. The concentrations of the PAHs ranged 88–1900 ng/g (average, 731 ng/g) with the predominance (56%) of benzo(e)pyrene (BeP). Though the PAHs had a similar trend of distribution in the sediment at both peri-urban and urban portions, total PAHs concentration at the peri-urban area was three times higher than that obtained in the urban area of the river due to relatively lower photo-degradation process caused by the thick rain forest in the area. Pyrolytic processes such as coal/wood burnings and emissions from gasoline and diesel engines were the PAHs sources. No dermal carcinogenic or non-carcinogenic health concerns were posed by the individual PAH; cancer risk and hazard quotient values were <10−6 and <1.0, respectively. The sediment PAHs posed a low ecological risk in all the sampling locations as the mean effects range-median quotient of the individual USEPA priority PAHs was ≤0.04. The potential environmental toxicity of the priority PAHs showed that benzo(a)pyrene (BaP) and indeno[1,2,3-cd]pyrene (IDcdP) dominated, accounting for 37% and 44% of the total toxicity, respectively. The low health and ecological risks posed by the PAHs sediment became significant given the number of tourists Osun River attracts annually festival, as well as the effects on the river ecosystem.