Temporal and spatial distribution of polycyclic aromatic hydrocarbons (PAHs) in the Danube River in Hungary.

The Danube is a significant transboundary river on a global scale, with several tributaries. The effluents from industrial operations and wastewater treatment plants have an impact on the river's aquatic ecosystem. These discharges provide a significant threat to aquatic life by deteriorating the quality of water and sediment. Hence, a total of 16 Polycyclic Aromatic Hydrocarbons (PAHs) compounds were analyzed at six locations along the river, covering a period of 12 months. The objective was to explore the temporal and spatial fluctuations of these chemicals in both water and sediment. The study revealed a significant fluctuation in the concentration of PAHs in water throughout the year, with levels ranging from 224.8 ng/L during the summer to 365.8 ng/L during the winter. Similarly, the concentration of PAHs in sediment samples varied from 316.7 ng/g in dry weight during the summer to 422.9 ng/g in dry weight during the winter. According to the Europe Drinking Water Directive, the levels of PAHs exceeded the permitted limit of 100 ng/L, resulting in a 124.8% rise in summer and a 265.8% increase in winter. The results suggest that the potential human-caused sources of PAHs were mostly derived from pyrolytic and pyrogenic processes, with pyrogenic sources being more dominant. Assessment of sediment quality standards (SQGs) showed that the levels of PAHs in sediments were below the Effect Range Low (ERL), except for acenaphthylene (Acy) and fluorene (Fl) concentrations. This suggests that there could be occasional biological consequences. The cumulative Individual Lifetime Cancer Risk (ILCR) exceeds 1/104 for both adults and children in all sites.

Organic toxicants and emerging contaminants in hospital interiors before and during the SARS-CoV2 pandemic: alkanes and PAHs.

Indoor pollution and deposition dust (DD), in particular, are acquiring concern, due to long exposure time and importance of intake by humans through contact and ingestion. Hospitals look a special category of sites, owing to peculiar contaminants affecting them and to presence of people prone to adverse effects induced by toxicants. Four in-field campaigns aimed at understanding the chemical composition of DD were performed in five Italian hospitals. Measurements were performed before (autumn 2019), during (spring 2021), and after (winter 2022) the peak of SARS-CoV2 and when restrictions caused by pandemic were revoked (winter 2023). Parallel measurements were made outdoors (2022), as well as in a university and a dwelling. Targeted contaminants were n-alkanes and polycyclic aromatic hydrocarbons (PAHs), while iso- and anteiso-alkanes were analyzed to assess the impact of tobacco smoking. Total n-alkanes ranged from 3.9 ± 2.3 to 20.5 ± 4.2 mg/g, with higher percentages of short chain homologs in 2019. PAHs ranged from 0.24 ± 0.22 to 0.83 ± 0.50 mg/g, with light congeners (≤ 228 a.m.u.) always exceeding the heavy ones (≥ 252 a.m.u.). According to carbon preference indexes, alkanes originated overall from anthropogenic sources. Microorganisms resulted to affect a hospital, and tobacco smoke accounted for ~ 4-20‰ of DD mass. As for PAH sources, the diagnostic concentration ratios suggested the concourse of biological matter burning and vehicle emission. Benzo[a]pyrene equivalent carcinogenic and mutagenic potencies of depositions at hospitals ranged ~ 9-39 µg/g and ~ 15-76 µg/g, respectively, which seems of concern for health. DD composition in hospitals was different from that outside the premises, as well as that found at university and at dwelling.

Impact of Atmospheric Conditions and Source Identification of Gaseous Polycyclic Aromatic Hydrocarbons (PAHs) during a Smoke Haze Period in Upper Southeast Asia.

Gaseous polycyclic aromatic hydrocarbons were measured in northern Thailand. No previous studies have provided data on gaseous PAHs until now, so this study determined the gaseous PAHs during two sampling periods for comparison, and then they were used to assess the correlation with meteorological conditions, other pollutants, and their sources. The total concentrations of 8-PAHs (i.e., NAP, ACY, ACE, FLU, PHE, ANT, FLA, and PYR) were 125 ± 22 ng m-3 and 111 ± 21 ng m-3, with NAP being the most pronounced at 67 ± 18 ng m-3 and 56 ± 17 ng m-3, for morning and afternoon, respectively. High temperatures increase the concentrations of four-ring PAHs, whereas humidity and pressure increase the concentrations of two- and three-ring PAHs. Moreover, gaseous PAHs were estimated to contain more toxic derivatives such as nitro-PAH, which ranged from 0.02 ng m-3 (8-Nitrofluoranthene) to 10.46 ng m-3 (1-Nitronaphthalene). Therefore, they could be one of the causes of local people's health problems that have not been reported previously. Strong correlations of gaseous PAHs with ozone indicated that photochemical oxidation influenced four-ring PAHs. According to the Pearson correlation, diagnostic ratios, and principal component analysis, mixed sources including coal combustion, biomass burning, and vehicle emissions were the main sources of these pollutants.

A century-long record of polycyclic aromatic hydrocarbon deposition in the Old Yellow River Estuary, China.

Polycyclic aromatic hydrocarbons (PAHs) are potential geochemical indicators for assessing the impact of human activities and can be used to reconstruct historical human activities. This study collected a 108 cm sediment core from the 5th lobe of the Yellow River Delta for the first time and analyzed the historical distribution characteristics of PAHs in this area. The results showed that the sedimentation history of the core was from 1908 to 2014. The average value of PAHs was 28.93 ng/g. Biomass and coal combustion sources were the main sources of PAHs in the low-value areas, while oil spill sources were the main sources in the significantly higher PAHs areas in the 1960s, mid-1980s, late 1990s, and late 2010s, which was consistent with the development history of Shengli Oilfield. Compared with global estuaries, the historical industrial activity intensity in this area was weaker.

Fine and ultrafine particle emission factors and new diagnostic ratios of PAHs for peat swamp forest fires.

Peatland fires are one of the major global sources of atmospheric particles. Emission factors for fine (PM1 and PM2.5) and ultrafine (PM0.1) particles and particle-bound polycyclic aromatic hydrocarbons (PAHs) from plants in the peat swamp forest (PSF), including Melaleuca cajuputi leaves, M. cajuputi branches, M. cajuputi bark, Lepironia articulata (Retz.) Domin, forest leaf litter and peat were measured in a laboratory combustion chamber. From these measurements, new PAH diagnostic ratios for fine and ultrafine particles were proposed for identifying the forest burning source. The new emission factors for PM were PM0.1: 0.03-0.33, PM1: 0.69-2.11 and PM2.5: 1.12-4.18 g/kg; for PM-bound PAHs, the factors were PM0.1: 5.7-166.0, PM1: 31.5-1338.9 and PM2.5: 36.3-3641.1 µg/kg. The predominant PAHs for PSF burning were Pyr, BbF, DBA (in PM0.1), Flu, DBA, BghiPe (in PM1), and BbF, DBA and BghiPe (in PM2.5). We also presented new diagnostic ratios for PSF burning, including BaP/(BaP + Chr): 0.39-0.75, BaP/(BaP + BbF): 0.21-0.47 and BaA/(BaA + Chr): 0.36-0.53. Moreover, the physical and chemical characteristics of ambient fine and ultrafine particles in the Kuan Kreng forest during the 2019 forest fire (FF) and 2021 non-forest fire (NFF) periods were investigated. The mean PM0.1, PM1 and PM2.5 concentrations during the FF period were approximately 3.5-4.4 times as high as those during the 2021 NFF period. New PAH diagnostic ratios of BaP/(BaP + BbF) versus BaP/(BaP + Chr) were able to identify PAH burning sources in PM1 and PM2.5 but were less clear for PM0.1, which was dominated by a single source - M. cajuputi. Chemical mass balance studies identified peat forest burning emissions as the main source of fine and ultrafine particles during the FF period. This study suggests that the new PAH diagnostic ratios can be used to identify the burning source for more precise source apportionment.

Emission profiles, source identifications, and health risk of polycyclic aromatic hydrocarbons (PAHs) in a road tunnel located in Xi'an, China.

Understanding the sources and characteristics of PM2.5-bound PAHs from traffic-related pollution can provide valuable data for mitigating air contamination from traffic in local urban regions. However, little information on PAHs is available regarding the typical arterial highway-Qinling Mountains No.1 tunnel in Xi'an. We estimated the profiles, sources, and emission factors of PM2.5-bound PAHs in this tunnel. The total PAH concentrations were 22.78 ng·m-3 and 52.80 ng·m-3 at the tunnel middle and exit, which were 1.09 and 3.84 times higher than that at the tunnel entrance. Pyr, Flt, Phe, Chr, BaP, and BbF were the dominant PAH species (representing approximately 78.01% of total PAHs). The four rings PAHs were dominant (58%) among the total PAH concentrations in PM2.5. The results demonstrated that diesel and gasoline vehicles exhaust emissions contributed 56.81% and 22.60% to the PAHs, respectively, while the corresponding value for together brakes, tyre wear, and road dust was 20.59%. The emission factors of total PAHs were 29.35 µg·veh-1·km-1, and emission factors of 4 rings PAHs were significantly higher than those of the other PAHs. The sum of ILCR was estimated to be 1.41×10-4, which accorded with acceptable level of cancer risk (10-6-10-4), PAHs should not ignored as they still affect the public health of inhabitants. This study shed light on PAH profiles and traffic-related sources in the tunnel, thereby facilitating the assessment of control measures targeting PAHs in local areas.

Seasonality of Polyaromatic Hydrocarbons (PAHs) and Their Derivatives in PM2.5 from Ljubljana, Combustion Aerosol Source Apportionment, and Cytotoxicity of Selected Nitrated Polyaromatic Hydrocarbons (NPAHs).

Airborne particulate matter (PM) is a vector of many toxic pollutants, including polyaromatic hydrocarbons (PAHs) and their derivatives. Especially harmful is the fine fraction (PM2.5), which penetrates deep into the lungs during inhalation and causes various diseases. Amongst PM2.5 components with toxic potential are nitrated PAHs (NPAHs), knowledge of which is still rudimentary. Three of the measured NPAHs (1-nitropyrene (1-nP), 9-nitroanthracene (9-nA), and 6-nitrochrysene (6-nC)) were detected in ambient PM2.5 from Ljubljana, Slovenia, along with thirteen non-nitrated PAHs. The highest concentrations of pollutants, which are closely linked with incomplete combustion, were observed in the cold part of the year, whereas the concentrations of NPAHs were roughly an order of magnitude lower than those of PAHs throughout the year. Further on, we have evaluated the toxicity of four NPAHs, including 6-nitrobenzo[a]pyrene (6-nBaP), to the human kidney cell line, HEK293T. The most potent was 1-nP (IC50 = 28.7 µM), followed by the other three NPAHs, whose IC50 was above 400 or 800 µM. According to our cytotoxicity assessment, atmospheric 1-nP is the most harmful NPAH among the investigated ones. Despite low airborne concentrations of NPAHs in ambient air, they are generally considered harmful to human health. Therefore, systematic toxicological assessment of NPAHs at different trophic levels, starting with cytotoxicity testing, is necessary in order to accurately evaluate their threat and adopt appropriate abatement strategies.

Investigation of the spatial distribution of airborne polycyclic aromatic hydrocarbons using Rhytidiadelphus squarrosus in Tórshavn, Faroe Islands.

Due to adverse effects of Polycyclic Aromatic Hydrocarbons (PAHs) on human health, it is important to understand how airborne PAHs, are spatially distributed within urban areas. Moss has been shown to be a suitable material for biomonitoring of airborne PAH pollution. In this study, the moss Rhytidiadelphus squarrosus was sampled throughout Tórshavn, Faroe Islands. 53 Rhytidiadelphus squarrosus samples were extracted using a matrix solid-phase dispersive extraction method and analysed for 19 parent PAHs and six groups of alkylated PAHs using gas chromatography mass-spectrometry. All PAHs were quantified in at least one Rhytidiadelphus squarrosus sample, and the sum of the EPA 16 PAHs (Æ©PAHEPA16) ranged from 0.90 to 344 µg kg-1 dry weight. Higher concentrations were found close to the harbour and the main roads. The spatial correlation was investigated for the Æ©PAHEPA16, pyrene, fluoranthene, chrysene, benzo(e)pyrene, benzo(g,h,i)perylene, C1-phenanthrenes/C1-anthracenes, and C2-phenanthrenes/C2-anthracenes using variograms. The effective range of the spatial correlation was between 500 to 700 m of all PAHs. The evaluation of diagnostic ratios of fluoranthene to pyrene, and benzo(a)anthracene to chrysene suggest that different pollution sources affect urban areas of different types. To the best of our knowledge, this is the first time airborne PAH pollution patterns were mapped in an Arctic town, and the first time, Rhytidiadelphus squarrosus was used for tracing PAH pollution sources. Rhytidiadelphus squarrosus is suitable for biomonitoring and mapping PAH pollution within urban areas since it is widespread, and suitable for mapping PAHs.

Biomonitoring of polycyclic aromatic hydrocarbons (PAHs) by Murraya paniculata (L.) Jack in South Kolkata, West Bengal, India: spatial and temporal variations.

Attempts have been made in the present study for ascertaining the concentrations of atmospheric polycyclic aromatic hydrocarbons (PAHs) using passive biosamplers in preference to conventional air sampling methods. Mechanical stirring, sonication, Soxhlet technique and microwave-assisted Soxhlet extraction (MASE) were employed to extract PAHs from an evergreen plant (Murraya paniculata) leaves (having long life-span) sampled from polluted places of South Kolkata, India, with dense population and heavy traffic. Effects of extraction methods and operational parameters (solvent and time) on the recovery levels of PAHs were also investigated. Purified extracts, acquired through adsorption chromatography, were subjected to GC-MS and HPLC-UV analyses for qualitative and quantitative assessment of PAHs. Spatio-temporal distribution of accumulated PAHs across the sampling sites was monitored over premonsoon, postmonsoon and winter supported by pollutant source characterization. The results displayed that the extraction yields of Soxhlet (272.07 ± 26.15 µg g-1) and MASE (280.17 ± 15.46 µg g-1) were the highest among the four techniques. Conditions of extraction with toluene for 6 h were found to be most favorable for PAHs. In spatio-temporal analysis, total concentrations of PAHs in the foliar samples varied from 200.98 ± 2.72 to 550.79 ± 10.11 µg g-1 dry weight, and the highest values being recorded in the samples of Exide More because of daylong inexorable traffic flow/crowding increasing the burden of ambient PAHs. Widespread changes in meteorology exerted influence on seasonal concentrations of PAHs in plant leaves, and extent of leaf contamination by PAHs was observed extreme in winter followed by postmonsoon and then, premonsoon. Foliar accretion of PAHs differed in the study sites with diverse sources of emission from motor vehicles, fossil fuel and biomass burning along with other human interferences.

Polycyclic aromatic hydrocarbons in the surface water and sediment along Euphrates River system: Occurrence, sources, ecological and health risk assessment.

This study presented for the first time a comprehensive measurement campaign of 16 PAHs along the Euphrates River for five months, in both water and sediment samples. Our study revealed that the PAHs contamination increased along the flow direction due to the increasing non-point pollution and the return flows of agriculture. The 5-6 rings PAHs were dominant in water and sediment samples with an average of 42 % and 50 %, respectively. The diagnostic ratios of PAHs suggest that the pollution of these compounds originated mainly from petroleum product combustions. The carcinogenic PAHs formed 46 % and 55 % of the total measured compounds in water and sediment samples, respectively, which highlights potential ecological and human health risks. Based on sediment quality guidelines (SQGs), most sites exhibit an effect range between low and medium. The calculated incremental lifetime cancer risk (ILCR) for adult and children were in the 10-2-10-3 range, which is 3-6-fold higher than what was reported in the literature. These observations call for urgent attention from environmental authorities of countries sharing this key water source in Western Asia.

Chemometric techniques in oil spill identification: A case study in Dalian 7.16 oil spill accident of China.

Chemometric methods have unique advantages regarding comprehensive consideration of multiple parameters and the classification of samples or variables. Classification of oil spill sources was carried out by using chemometric techniques, such as Repeatability Limit, hierarchical cluster analysis (HCA), Student's t-test and Principal component analysis (PCA) Biplot. In addition, this paper takes the fingerprint identification of a Dalian "7.16″ oil spill accident as an example to illustrate the effectiveness of chemometric techniques in oil identification. PCA scores plot (explaining 82.77% of variance accounted for three PCs) showed that samples belong to four clusters and result of HCA method further confirmed that. The residual oil in Jinshatan Beach and Haibei Square may be caused by the explosion of Dalian "7-16" oil pipeline accident. The use of chemometric techniques is significant in providing independent validation for classifying the types of spilled oil in the investigation of oil spill pollution. The results will be of great significance to improve the accuracy and efficiency of oil spill identification based on oil fingerprint.

The first high resolution PAH record of industrialization over the past 200 years in Liaodong Bay, northeastern China.

Polycyclic aromatic hydrocarbons (PAHs) are excellent tracers for fossil fuel combustion, natural fires and petroleum contamination, and have been widely used for reconstructing past wildfires and industrial activities at a variety of time scales. Here, for the first time, we obtain a high resolution (annual to decadal scale) record of PAHs from two parallel marine sediment cores from the Liaodong Bay, Northeastern China to reconstruct the industrial activities, spanning the past ∼ 200 years from 1815 to 2014. Our data indicate that PAH variations can be divided into four episodes: I) low (probably near background) PAHs from natural fires and domestic wood combustion during the pre-industrial period from 1815 to 1890; II) slightly increased (but with large fluctuations) PAH concentrations derived from intermittent warfare during the World War (1891-1945) and increased industrial activities after 1946 (1946-1965); III) a period of stagnation and, in some cases, reduction in PAHs during the "Cultural Revolution" (1966 to 1979); and IV) a rapid and persistent rise in PAHs post 1979 linked to fast economic development, with PAH concentrations doubled from 1979 to 2014. Changes in PAH distributions demonstrate major shifts in the dominant types of fuels over time from vegetation/wood, to coal and wood, followed by coal and petroleum (including vehicle emissions) over the past 200 years. We find that PAH records also show similar trend to domestic economy and the estimated regional Anthropocene CO2 emissions from industrial activities, suggesting sedimentary PAH fluxes could be used as an indirect and qualitative proxy to track the trend for regional anthropogenic CO2 emissions.

Spatial and temporal trends of polycyclic aromatic hydrocarbons in sediment cores of Brunei Bay, East Malaysia.

The spatial and temporal distribution of polycyclic aromatic hydrocarbons (PAHs) in three sediment cores from Brunei Bay, Southern South China Sea was investigated. The total concentrations of 16 priority PAHs (∑PAH16) and their alkyl-substituted derivatives ranged from 10.4 to 376 ng g-1 and 30.7 to 2263 ng g-1, respectively. PAH biomarker diagnostic ratios and principal component analysis (PCA) combined with absolute principal component score (APCS) and multiple linear regression (MLR) were performed to apportion the source contribution. The results revealed mixed inputs of fuel combustion residues and uncombusted petrogenic products. The downcore PAH profile revealed that the highest peaks could be related to past human activities using biofuel and coal during the industrialization/agriculture revolution period. The 1,7/(2,6+1,7)-dimethylphenanthrene ratio also highlighted wood combustion during forest fire outbreaks, which appeared to coincide with the past climate events.

Atmospheric levels, distribution, sources, correlation with meteorological parameters and other pollutants and health risk of PAHs bound in PM2.5 and PM10 in Burgas, Bulgaria - a case study.

The quality of atmospheric air of Burgas city, Bulgaria was analyzed in relation to PAHs in two particulate matter fractions - 2.5 µm and 10 µm. It was found that PAHs registered in PM10 represent entirely the ones registered in PM2.5 - an indication that the particulate PAHs in ambient air of Burgas for the sampling period are associated with the fine PM fraction. The PAH compounds with highest concentrations are mainly associated with coal combustion, diesel and gasoline vehicle and biomass burning, which is further confirmed by the calculated diagnostic ratios. The combustion-derived PAHs represent on average 86.6 ± 2.8% of total PAHs concentration. The linear regression analysis showed strong and statistically meaningful correlations between PM fractions and PAHs indicating the influence of similar local events and emission sources of pollution. PM2.5 or PM10 relationships with PAHs were significant but lower correlation coefficients were observed for low-molecular weight (LMW) PAHs in comparison to middle-molecular weight (MMW) and higher-molecular weight (HMW) PAHs, due to their lower presence in particulates and higher partition in gaseous atmospheric phase. Further significant correlations were found with wind speed, solar radiation and atmospheric pressure as well as NO2 and O3 ambient concentration. The calculated excess cancer risks are twice as much as acceptable limit.

Characteristics, influence factors, and health risk assessment of volatile organic compounds through one year of high-resolution measurement at a refinery.

From January 2020 to December 2020, high-resolution data of volatile organic compound (VOC) concentrations were monitored by online instruments at a petroleum refinery. The measurement results showed that the external contaminants, meteorological conditions and photochemical reactions had a great influence on the VOC data measured in the petroleum refineries. Some significant differences were observed in the emission composition of different refineries, while propene (34.2%), propane (10.2%), n-butane (5.6%), i-pentane (5.0%) were the dominant species emitted from the refinery in this study. The correlations between compounds with similar atmospheric lifetimes were strong (R2 > 0.9), which indicated that the diagnostic ratios of these compounds could be used as indicators to identify the refinery emission source. Chronic health effects of non-carcinogenic risk results showed that acrolein had the highest non-carcinogenic risk and other compound-specific health risks may be of less concern in the refining area. Halogenates and aromatics accounted for 97.4% of the total carcinogenic risk values, while 1,2-dibromoethane, chloromethane, benzene, trichloromethane, 1,2-dichloroethane contributed approximately 80% of the total carcinogenic risk assessment values. This research has recorded valuable data about the VOC emission characteristics from the perspective of the high-resolution monitoring of the petroleum refinery. The results of this work will provide a reference to accurately quantify and identify the emission of petroleum refineries and further throw some light on effective VOC abatement strategies.

Concentration, source apportionment and potential carcinogenic risks of polycyclic aromatic hydrocarbons (PAHs) in roadside soils.

PAHs are organic pollutants that have carcinogenic and mutagenic impacts on human health and are a subject of great concern. The soil-bound polycyclic aromatic hydrocarbons (PAHs) in the urban areas can be very lethal to human health. The concentrations, sources, and possible cancer risks of 15 PAHs were analysed by collecting roadside soil samples in Lucknow, India. The range of ∑15PAHs was found to be 478.94 ng/g to 8164.07 ng/g with a mean concentration of 3748.23 ng/g. The highest contribution (32.5%) was found to be from four-ring PAHs, followed by six-ring (24.5%) and five-ring (16.7%) PAHs. The source apportionment through diagnostic ratios ANT/(ANT + PHE) against FL-2/(FL-2+PYR) highlighted the dominance of petroleum, wood, coal, and grass combustion as sources of PAHs in the study area. Source apportionment was also done through positive matrix factorization, confirming the dominance of 'vehicular emissions' (49%), followed by 'coal and biomass combustion' (∼39%), and 'leakages, volatilization and petroleum combustion' (∼12%) as potential sources. The results from lifetime cancer risks (ILCR) varied in the range of 7.5 × 10-4 and 1.3 × 10 × -2 illustrating 'high cancer risk'. The total cancer risk susceptibility of children was found to be 31% more than that of adults. The highest risk associated with toxic equivalent concentration (TEQ) was found at site S8 highlighting the impact of the presence of an international airport, and huge traffic load. The present study will prove to be useful for information related to human exposure to PAHs content in soil in the study area and as baseline study for policy makers, stakeholders, and researchers.

Polycyclic aromatic hydrocarbons in coastal sediments of Southern Terengganu, South China Sea, Malaysia: source assessment using diagnostic ratios and multivariate statistic.

Surface sediments along the Southern Terengganu coast (≤7 km from the coast) were analyzed for polycyclic aromatic hydrocarbons (PAHs). The concentrations of 16 USEPA priority polycyclic aromatic hydrocarbons (ΣPAH16) ranged from 2.59 to 155 ng g-1 and their respective alkylated ranged between 8.80 and 24.90 ng g-1. Traces of acephenanthrylene, benzo[c]phenanthrene, thiophenic PAH, and benzonaphthofuran were identified. PAH diagnostic ratios and cross-plots revealed that these sedimentary PAH compounds are derived mainly from pyrogenic sources, primarily from biomass burning and petroleum combustion residues with minor petrogenic input. The high correlations between pyrogenic PAHs to total PAHs (r >0.73, p <0.5), and the Bap/Bep ratio to total PAHs (r = 0.88, p <0.5), suggest that atmospheric deposition and urban runoff are the main deposition pathways. The concentrations of the PAHs in the southern South China Sea fall in the moderate contamination range of 100-1000 ng g-1.

Placental levels of polycyclic aromatic hydrocarbons (PAHs) and their association with birth weight of infants.

As an alarming group of pollutants, polycyclic aromatic hydrocarbons (PAHs) gather much public health concern not only because of their carcinogenic or co-carcinogenic risk but also by interfering with hormone systems or by causing oxidative damage, henceforth liable to toxic actions on reproduction. Accordingly, the present study was aimed to explore the association between in-utero exposure to PAHs by evaluating their placental levels and infant birth weight among 110 healthy and nonsmoking pregnant women. Placental tissue samples were collected instantly after delivery and were analyzed for the presence of sixteen Environmental Protection Agency (EPA) listed PAHs with the help of Gas chromatography equipped with flame ionization detector (GC-FID). Chrysene and benzo(k)fluoranthene were the predominant PAHs detected in tissue samples. To assess the source of origin of PAHs in placenta tissue samples, the ratio of low molecular weight PAHs to high molecular weight (∑LMW/∑HMW PAHs) was calculated, showing the predominance of pyrogenic sources of PAHs possibly responsible for the exposure of the studied population. Results of regression analysis demonstrated the inverse although not significant association of naphthalene (Nap), acenaphthylene (Acy), anthracene (Anth), pyrene (Pyr), benzo(b)fluoranthene (BbF), benzo(k)Fluoranthene (BkF), benzo(a)pyrene (BaP), indeno (123 cd pyrene (IcdP), dibenzo(ah)anthracene (DahA) and benzo(ghi)Perylene (BghiP) with birth weight of neonates. Additionally, the regression model lay light upon the significant association of fluoranthene (Fla) (coefficient= -1.41 gram, p < 0.05) to the depletion trend of birth weight after adjusting for potential covariates. These findings suggest the possible role of an environmental contaminants like PAHs on impairment of fetal growth.

[Characteristics of BTEX and Health Risk Assessment During Typical Pollution Episodes in Summer and Winter in Tianjin Urban Area].

Real-time BTEX(including benzene, toluene, ethylbenzene, m-, p-, and o-xylenes) were measured continuously in Tianjin urban site in July 2019 and January 2020 using a Syntech Spectras GC955 analyzer. The BTEX concentration levels, composition, and evolutionary mechanisms during typical pollution episodes were investigated. The potential sources of BTEX were analyzed qualitatively using the diagnostic ratios method. Finally, the BTEX health risk was evaluated by using the human exposure analysis and evaluation method according to US EPA. The averaged total mixing ratio of BTEX were 1.32×10-9 and 4.83×10-9 during ozone pollution and haze episodes, respectively. Benzene was the most abundant species, followed by toluene. The mixing ratio of BTEX was largely affected by short southwestern distance transportation in January, while local emissions in July. In addition, the BTEX mixing ratio depended on the influence of temperature and relative humidity(RH) in July, while the concentration was more sensitive to changes in RH when the temperature was low in January. Diagnostic ratios and source implications suggested that the BTEX was affected mainly by biomass/biofuel/coal burning during haze episodes. The traffic related emissions also had an impact except for the influence of biomass/biofuel/coal burning in July. The averaged hazard quotient(HQ) values were 0.072 and 0.29 during ozone pollution and haze episodes, respectively, which were in the upper safety range limit recommended by the US EPA. The carcinogenic risk posed by benzene in both cleaning and pollution processes was higher than the safety threshold set by the US EPA, which should be monitored carefully.

Oil spill fingerprint of low sulfur fuel oil in South Korea.

A low sulfur fuel oil (LSFO) spill accident occurred in South Korea on December 17, 2019, before the introduction of the International Maritime Organization (IMO) sulfur limit. In this study, chromatograms, percentage weathering plots (PW-plots), and diagnostic ratios (DRs) of LSFOs collected in different areas during in the early spillage were compared for oil spill fingerprint. The source oil was conformed as LSFO according to physical properties and spill oils, like the source oil, show high n-alkanes and low benzo[b]naphto[1,2-d]thiophene (BNT) distribution. In the PW-plots, spill oils exhibited a decreasing trend with the reduction of low-molecular-weight compounds, which were affected by evaporation. The relative difference in the DRs was below 14%, indicating that the source and spill oils matched, excluding the ratios consisting of evaporated compounds. These results showed that spill oils confirmed as LSFO were evaporated during the initial spillage stage, and matched to the source oil.