Low Polycyclic Aromatic Hydrocarbons Concentrations Research Articles

The perturbation of PAHs on mosses in Aberdeen, Scotland, as a consequence of social restrictions imposed during the COVID-19 pandemic

Air quality and the concentration of polycyclic aromatic hydrocarbons (PAHs) in urban environments are increasingly becoming a concern. Measuring air quality and PAHs, and linking these to specific activities, requires deploying and recovering sampling devices to capture and measure any changes. From May 2020 to June 2021, during the “lockdown” period of the COVID-19 pandemic, acrocarpous and pleurocarpous mosses were collected from five types of site in Aberdeen, United Kingdom, and the concentration of PAHs measured to track changes in PAHs as travel-related activities changed. The predominant types of PAHs found on mosses were of the four- and five-ring varieties, with the four-ring variety of PAH (medium molecular weight) becoming more dominant as the lockdown was lifted. However, for most sites, the concentration of PAHs was evidently perturbed by the transient lifting, reimposing, and then lifting of lockdown conditions, which either directly limited travel or changed people’s motivations to travel by car. Molecular diagnostic ratios or molecular marker parameters used to infer the source of PAHs varied little and were nearly always consistent with PAHs deriving from combustion in vehicle engines. Thus, even when travel was limited, PAHs were still derived from vehicle usage, although the overall concentrations on mosses were much lower. On average, the lowest PAH concentrations were found on mosses collected from a recreational park located the furthest from traffic. The highest PAH concentrations were observed on mosses collected from residential car parks during periods when the lockdown had been lifted. However, mosses from the same residential car parks had very low PAH concentrations during periods of travel restrictions, strongly suggesting that, for mosses, local factors and patterns of vehicle usage strongly determine their exposure to PAHs. Therefore, mosses within urban environments can be used for monthly monitoring of PAHs as they are able to detect changes induced by human behaviour.

Mechanisms and targeted reversion/prevention of hepatic fibrosis caused by the non-hereditary toxicity of benzo(a)pyrene

The effect of long term exposure to low concentrations of environmental pollutants on hepatic disorders is a major public health concern worldwide. Polycyclic aromatic hydrocarbons (PAHs) are a class of persistent organic pollutants. In recent years, an increasing number of studies have focused on the deleterious effects of low concentrations of PAHs in the initiation or exacerbation of the progression of chronic liver disease. However, the underlying molecular mechanisms and effective intervention methods remain unclear. Here, we found that in hepatocytes, a low concentration of benzo(a)pyrene (B[a]P, an indicator of PAHs) chronic exposure continuously activated 14-3-3η via an epigenetic accumulation of DNA demethylation. As a “switch like” factor, 14-3-3η activated its downstream PI3K/Akt signal, which in turn promoted vascular endothelial growth factor (VEGF) production and secretion. As the characteristic fibrogenic paracrine factor regulated by B[a]P/14-3-3η, VEGF significantly induced the neovascularization and activation of hepatic stellate cells, leading to the development of hepatic fibrosis. Importantly, targeted 14-3-3η by using its specific inhibitor invented by our lab could prevent B[a]P-induced hepatic fibrosis, and could even reverse existent hepatic fibrosis caused by B[a]P. The present study not only revealed novel mechanisms, but also proposed an innovative approach for the targeted reversion/prevention of the harmful effects of exposure to PAHs on chronic liver disease.

Spatial distribution and partition of polycyclic aromatic hydrocarbons (PAHs) in the water and sediment of the southern Bohai Sea: Yellow River and PAH property influences

The marginal Bohai Sea, connected to the northwestern Pacific Ocean, is threatened by human activity. The Yellow River, the second largest river in China, drains large amounts of water, silts, and polycyclic aromatic hydrocarbons (PAHs) into the southern Bohai Sea; however, to what extent the Yellow River inputs influence the spatial distributions and partitions of PAHs in the southern Bohai Sea is not well known. Therefore, this study collected surface water, bottom water, and sediment samples from the southern Bohai Sea and analyzed them to examine the spatial distributions and partitions of 15 priority PAHs. The results showed that PAH concentrations ranged from 26.9 to 50.1 ng L–1 in surface water, 18.8 to 44.1 ng L–1 in bottom water, and 7.4 to 143.9 ng g–1 in sediment, with higher proportions of four-, five-, and six-ring PAHs in sediment than in water. PAH inputs from the Yellow River and sea coastal currents determined the spatial distribution of PAH concentrations in water and sediment, with an overall decrease from the estuary to the southeast. However, the solid dilution effect of input silts from the Yellow River and the liquid dilution effect of water from the Yellow River and Yellow Sea led to lower PAH concentrations in the water and sediment of the southern Bohai Sea than those in other areas of the Bohai Sea. PAH exchange between the atmosphere and seawater led to significantly higher individual PAH concentrations (except for acenaphthylene) in the surface water than in the bottom water, with ratios significantly related to the PAH n-octanol-water partition coefficient, organic carbon-water partition coefficient, and Henry's law constants. These parameters also determined PAH partitioning between the bottom water and sediment. Individual and total PAH concentrations in the sediment were significantly correlated with organic matter, clay, and silt contents. Therefore, the partitions and spatial distributions of PAHs in the southern Bohai Sea comprehensively depend on PAH properties, PAH inputs from the Yellow River and the atmosphere, sea currents, and seawater and sediment properties. The ecological risks posed by individual PAHs in both water and sediment were negligible or acceptable.

Association between PAH and plastic fragments on Brazilian coast beaches: a baseline assessment.

Plastic materials have many destinies on the environment, and one of them is its continuous fragmentation, originating microplastics (MP). MP act as an adsorption surface for organic pollutants like polycyclic aromatic hydrocarbons (PAH). Due to its toxic and harmful properties, 16 PAH are defined as priorities in studies. Several works have evaluated the occurrence of MP and PAH individually in environmental matrices, but just a few have investigated their association. The present study aims to investigate PAH occurrence, sources, and concentration in MP from beach sediments of eight Brazilian coastal states. Sixteen PAH were analyzed by gas chromatography, in which 14 PAH were detected, and PAH total concentration (ΣPAH) ranged from 0.25 to 71.60ngg-1. In the North and Northeast regions, the low PAH concentrations in MP appear to be related to the intense hydrodynamic processes. Naphthalene levels on the Styrofoam were above the threshold effect level in two samples and near it on one; therefore, effects in the organisms might occur due to these PAH. The Southeast and South regions are the only ones with previous studies relating PAH with MP, and ΣPAH ranged from 0.34 to 2.52ngg-1. According to the diagnostic ratios, the PAH sources were associated with industrial and port activities, untreated effluent disposal, and urban runoff by pluvial waters. The highest ΣPAH level was found in the Styrofoam samples, suggesting that this MP type might contribute considerable to PAH dispersion on Brazilian coast beaches.

Ecological and health risk assessments of polycyclic aromatic hydrocarbons (PAHs) in soils around a petroleum refining plant in China: A quantitative method based on the improved hybrid model

Polycyclic aromatic hydrocarbons (PAHs) are extensively released into the environment by petroleum refining activities, predominantly affecting soil as a major reservoir. This study focuses on an active petroleum refinery in central China and employs a multi-faceted approach, combining geo-statistics, the absolute principal component-multiple linear regression model, and the Monte Carlo simulation, to comprehensively unravel the sources and risks associated with 12 PAHs. The analysis reveals a wide range of PAH concentrations, spanning from 60.23 to 1678.00 μg·kg−1, with an average of 278.91 μg·kg−1. Strikingly elevated PAH levels are primarily concentrated in construction and transportation lands, whereas woodland and grasslands exhibit lower PAH concentrations. In terms of ecological impact, the risk arising from oil-coal combustion significantly surpasses that linked to biomass combustion. meticulous assessments indicate negligible carcinogenic risks for both children and adults within the study area. An innovative hybrid model, which seamlessly integrates risk assessments with source identification, emerges as a pivotal advancement. This hybrid model not only quantifies PAH emission levels from refining activities but also effectively quantifies potential risks from distinct sources. Consequently, this study furnishes a robust theoretical foundation for strategizing PAH pollution risk mitigation. In essence, our research not only contributes a comprehensive understanding of PAH distribution around an active petroleum refinery but also introduces an advanced hybrid model, culminating in valuable insights for devising measures to curtail PAH-related environmental risks.

Distribution, composition and risk assessment of PAHs and PCBs in cryospheric watersheds of the eastern Tibetan Plateau

Polycyclic Aromatic Hydrocarbons (PAHs) and Polychlorinated Biphenyls (PCBs) are significant components of persistent organic pollutants (POPs) and pose a threat to both ecosystems and human health. To explore their spatial distribution, origins, and risk assessment, we collected 25 glacial meltwater and downstream river water samples in the eastern Tibetan Plateau (including the Qilian Mountains in the northeast) during the summer of 2022 (June–July). Our results showed that ∑PAHs and ∑PCBs were present in a wide range from ND-1380 ng/L and ND-1421 ng/L, respectively. Compared to other studies worldwide, the ∑PAHs and ∑PCBs in the Hengduan Mountains were at high levels. The PAHs and PCBs mainly consisted of low-molecular-weight homologs, including Ace, Flu, Phe, and PCB52. Phe was the primary component of PAHs. Glacial meltwater samples generally exhibited low concentration of PAHs and PCB52, whereas downstream river water samples typically showed high concentration of PAHs and PCB52. We attributed this characteristic to the influence of pollutants physicochemical properties, altitude effect, long-range transport (LRT), and local environmental conditions. In the eastern Tibetan Plateau glacier basin (especially in the Hailuogou watersheds), the concentration of PAHs and PCB52 in runoff generally increased with decreasing elevation. We believe that the primary factor affecting the concentration of PAHs and PCB52 in the region is the difference in local human activity inputs from various altitudes. The composition characteristics of PAHs and PCBs suggested that incomplete coal combustion and coking discharge mainly caused PAHs, while the combustion of coal and charcoal and the release of capacitors primarily caused PCBs. We assessed the carcinogenic risk of PAHs and PCBs in the glacier basin of the TP and found that the potential threat of PAHs was stronger than that of PCBs. Overall, this study provides new insights into the ecological security of water resources in eastern Tibetan Plateau. It is significant for controlling PAHs and PCBs emissions, assessing the ecological environment of the glacier watershed, and regional human health.

ASSESSMENT OF RIVER SEDIMENT QUALITY ACCORDING TO THE EU WATER FRAMEWORK DIRECTIVE IN LARGE RIVER FLUVIAL CONDITIONS. A CASE STUDY IN THE LOWER DANUBE RIVER BASIN

Increase of pollution of surface water and water sediments with hazardous substances (HSs) in the Danube River Basin requires implementation of systematic monitoring and evaluation of the sediment quality. The present study is focused on the ’South Danube’ Test Area (SDTA) that covers parts of the Lower Danube Basin in Romania, Serbia and Bulgaria. The SD area represents an extended region where Danube reaches its largest widths and depths and where pollution (industrial, mining, agricultural, waste etc.) from tributaries and land is supposed to accumulate in the sediments. Sampling of river bottom sediment (BS), suspended sediment (SS) and overbank (floodplain) sediment at two layers (0-5 cm in the top layer (FS TS) and 40-50 cm in the bottom layer (FS BS)), was carried out at 11 locations in order to analyze the concentration and distribution of 8 metal(oid)s (Cu, Pb, Zn, Cd, Hg, Ni, Cr, As), 6 polycyclic aromatic hydrocarbons (PAHs) and 6 pesticides as hazardous substances. The 2013/39/EU Directive and EU Water Framework Directive standards were used to sediment quality assessment. As a whole, the concentrations of heavy metals in the sediments are comparatively low and are around the normal values for soils. On the other hand, some sampling sites and sediment types have high or very high metal concentrations which exceed intervention levels. Our study well recognizes mining pollution sources in the Danube tributaries Borska Reka, Timok, Ogosta, Malak Iskar and Iskar from past and/or recent mining activity. This pollution is limited to the Danube tributaries and around their confluences into the Danube River. The concentration of heavy metals is strongly diluted in the Danube River and drops around normal values. The studied sediments reveal low concentrations of PAHs. Only fluoranthene content is higher in most of the sediment types and sampling sites on the Danube River, but exceeds the interventional level only at Pristol and at Hârșova. Our results show that the sediments in the Danube River are more polluted with PAHs than its tributaries. The identified organic compounds are assumed to be generated during incomplete or low temperature combustion processes or during road transportation and/or the navigation on the Danube River.

Polycyclic aromatic hydrocarbons (PAHs) levels in PM10 and bulk deposition using Mosspheres: A pilot study in an urban environment

Study air polycyclic aromatic hydrocarbons (PAHs) capturing the spatial variability of their concentrations is not economically feasible with conventional methods. In the present work we tested, for the first time and under real conditions, the suitability for intensive monitoring and mapping these contaminants of innovative, cost-effective passive air samplers known as “Mosspheres”. The Mosspheres, filled with a devitalised Sphagnum palustre L. moss clone, were placed in a 575 m. grid in a medium-sized European city for three months. Concentrations in the moss tissues of 15 priority PAHs, including benzo(a)pyrene, were determined and converted into PM10 and bulk deposition with the equations proposed in a recent study. Low concentrations of PAHs were detected, with only a few enriched points never exceeding the legal thresholds, near industrial areas and busy roads. Despite these low PAH concentrations, Mosspheres were able to detect spatial structure for several PAHs and high-resolution pollution maps were constructed for these compounds. The results prove the high sensitivity and suitability of Mosspheres for mapping PAH levels and for quantitative (i.e. PAHs with 4 or more rings) and qualitative (3-ring PAHs) monitoring. Thus, this study supports their widespread application and its potential inclusion in European Directives on air quality control.

Long-term exposure to low concentrations of polycyclic aromatic hydrocarbons and alterations in platelet indices: A longitudinal study in China.

Long-term exposure to low polycyclic aromatic hydrocarbon (PAH) concentration may ave detrimental effects, including changing platelet indices. Effects of chronic exposure to low PAH concentrations have been evaluated in cross-sectional, but not in longitudinal studies, to date. We aimed to assess the effects of long-term exposure to the low-concentration PAHs on alterations in platelet indices in the Chinese population. During 2014-2017, we enrolled 222 participants who had lived in a village in northern China, 1-2 km downwind from a coal plant, for more than 25 years, but who were not employed by the plant or related businesses. During three follow-ups, annually in June, demographic information and urine and blood samples were collected. Eight PAHs were tested: namely 2-hydroxynaphthalene, 1-hydroxynaphthalene, 2-hydroxyfluorene, 9-hydroxyfluorene (9-OHFlu), 2-hydroxyphenanthrene (2-OHPh), 1-hydroxyphenanthrene (1-OHPh), 1-hydroxypyrene (1-OHP), and 3-hydroxybenzo [a] pyrene. Five platelet indices were measured: platelet count (PLT), platelet distribution width (PDW), mean platelet volume (MPV), platelet crit, and the platelet-large cell ratio. Generalized mixed and generalized linear mixed models were used to estimate correlations between eight urinary PAH metabolites and platelet indices. Model 1 assessed whether these correlations varied over time. Models 2 and 3 adjusted for additional personal information and personal habits. We found the following significant correlations: 2-OHPh (Model1 β1 = 18.06, Model2 β2 = 18.54, Model β3 = 18.54), 1-OHPh (β1 = 16.43, β2 = 17.42, β3 = 17.42), 1-OHP(β1 = 13.93, β2 = 14.03, β3 = 14.03) with PLT, as well as 9-OHFlu with PDW and MPV (odds ratio or Model3 ORPDW[95%CI] = 1.64[1.3-2.06], ORMPV[95%CI] = 1.33[1.19-1.48]). Long-term exposure to low concentrations of PAHs, indicated by2-OHPh, 1-OHPh, 1-OHP, and 9-OHFlu, as urinary biomarkers, affects PLT, PDW, and MPV. 9-OHFlu increased both PDW and MPV after elimination of the effects of other PAH exposure modes.

Photocatalytic air purification of polycyclic aromatic hydrocarbons: Application of a flow-through reactor, kinetic studies and degradation pathways

This study investigates the performance of a newly developed flow-through reactor and the utilized photocatalytic materials in two environments: a lab-scale experiment and a pilot-scale experiment in a contaminated building. The aim was to assess the removal of polycyclic aromatic hydrocarbons from the air using an innovative reactor equipped with an ultraviolet-irradiated titanium dioxide catalyst. Empirical measurements were conducted in the laboratory to revise the developed fixated titanium dioxide catalysts at different irradiances. Naphthalene and 1-methylnaphthalene elimination were used as model substances due to being the most volatile polycyclic aromatic hydrocarbons (PAH). In addition, they are often found in contaminated buildings. Tests in an office building revealed high suitability of the air cleaning system for low polycyclic aromatic hydrocarbons concentrations with a degradation of the compounds below the allowed limits of indoor air pollutants set by the German Federal Ministry for the Environment, Nature Conservation and Nuclear Safety. The degradation of the organic micropollutants proceeded without detection of by-products, so that mineralization can be assumed. Based on these observations and a large number of previous studies, detailed degradation pathways for the selected micropollutants were also established.

PM2.5‐Bound Polycyclic Aromatic Hydrocarbons (PAHs), Nitrated PAHs (NPAHs) and Oxygenated PAHs (OPAHs) in Typical Traffic‐Related Receptor Environments

AbstractPM2.5‐bound polycyclic aromatic hydrocarbons (PAHs), nitrated PAHs (NPAHs) and oxygenated PAHs (OPAHs) around roadside, port and airport areas were investigated to evaluate the impacts of vehicle, ship and aviation emissions on PAHs and their derivatives in relevant receptor environments. The PAHs concentrations in fuels increased in the following order: jet fuel < heavy fuel oil for vessel < automobile diesel fuel. However, the average mass ratio concentrations of PM2.5‐bound PAHs in roadside, port and airport areas were 42.9, 158.7 and 260.4 μg/g, respectively. The low PAHs concentrations in fuel were relevant to the high PAHs emissions. The composition of the molecular species showed that 5‐ and 6‐rings PAHs were dominated in roadside area, while 3‐ and 4‐rings PAHs were major proportions in port and airport areas. The average mass ratio concentrations of PM2.5‐bound NPAHs and OPAHs concentrations in roadside, port and airport areas were 23.5 and 115.2, 4.8 and 39.9, and 26.4 and 284.2 μg/g, respectively. The different variation tendencies between PAHs and their derivates, dominant individual NPAHs, diagnostic ratios of NPAH isomers and principal component analysis revealed that primary emission was the major contributor to NPAHs and OPAHs in three receptor environments, and secondary formation played non‐negligible roles in NPAHs formation in roadside and airport areas. In addition, 9‐nitroanthracene (9‐NAnt) and anthraquinone (ATQ) were found to be the indicatory compounds for traffic emission. Taken together, these results may provide a basic information for assessing the impact of traffic emission sources on PAC emissions to the related receptor environment.

Polycyclic aromatic hydrocarbons at subcritical levels as novel indicators of microbial adaptation in a pre-industrial river delta

Marine sediment is considered a vast sink for organic pollutants including polycyclic aromatic hydrocarbons (PAHs). However, little is known about the relationship between subcritical PAH allocation and benthic microbial patterns. Thus, we carried out a field investigation at the abandoned Yellow River Delta (AYRD) to deepen the understanding of PAHs' horizontal distribution and ecological roles on the continental shelf. The PAH level in the AYRD is relatively low and distance-independent, indicating it resulted from long-term, chronic, anthropogenic input. The combined application of diagnostic molecular ratios reported inconsistent PAH sources, which might be due to the low PAH concentrations and the complexity of contributing sources. Positive Matrix Factorization provided a more robust source classification and identified three main PAH sources—coal combustion and vehicle emissions, petrogenic process, and fossil fuels. The benthic microbiome did not show a significant response to PAHs in terms of microbial assemblage or alpha-diversity. However, Operational Taxonomic Units in some specific phyla, like Thaumarchaeota, Proteobacteria, Acidobacteria, and Chytridiomycota, correlated with the PAH source indicators, supporting the notion that PAH source indicators can act as a novel environmental indicator for microbial adaption. What's more, Microbial Ecological Networks show more connection at sites identified as biomass combustion by both Fluoranthene/(Fluoranthene + Pyrene) and Indeno(1,2,3-cd)pyrene/(Indeno(1,2,3-cd)pyrene + Benzo(ghi)perylene) compared to the ones identified as biomass combustion by Fluoranthene/(Fluoranthene + Pyrene) and petroleum combustion by Indeno(1,2,3-cd)pyrene/(Indeno(1,2,3-cd)pyrene + Benzo(ghi)perylene). Herein, we demonstrate that the PAHs' source indicator can serve as a novel indicator of the interactions between microorganisms, and thus, should be applied to the sustainable management effort in the offshore area.

Plant contribution to the remediation of PAH-contaminated soil of Dagang Oilfield by Fire Phoenix.

Pot experiments were conducted to evaluate plant contribution during remediation of the polycyclic aromatic hydrocarbons (PAH)-contaminated soil of Dagang Oilfield by Fire Phoenix (a mixture of Festuca L.). The results showed that Fire Phoenix could grow in soil contaminated by high and low concentrations of PAHs. After being planted for 150days, the total removal rate of six PAHs in the high and low PAH concentrations was 80.36% and 79.79%, significantly higher than the 58.79% and 53.29% of the unplanted control group, respectively. Thus, Fire Phoenix can effectively repair the soil contaminated by different concentrations of PAHs. In high concentrations of PAHs, the results indicated a positive linear relationship between PAH absorption in tissues of Fire Phoenix and the growth time in the early stage. In contrast, the contents of PAHs were just slightly increased in the late period of plant growth. The main factor for the dissipation of PAHs was plant-promoted biodegradation (99.04%-99.93%), suggesting a low contribution of PAH uptake and transformation (0.07%-0.96%). The results revealed that Fire Phoenix did not remove the PAHs in the soil by accumulation but promoted PAH dissipation in the soil by stimulating the microbial metabolism in the rhizosphere.

Optimization of a Low Volume Extraction Method to Determine Polycyclic Aromatic Hydrocarbons in Aerosol Samples

This work describes the optimization of an extraction method for the determination of polycyclic aromatic hydrocarbons (PAHs) and their nitro- and oxy-PAH derivatives in atmospheric particulate matter (PM) samples, and demonstrates that this method is also effective for the determination of levoglucosan. The optimization of the extraction solvents was performed using a three-component mixture design with the solvents dichloromethane, methanol, and acetonitrile. The number of extractions, volume of solvent, and duration of extraction in an ultrasonic bath were optimized using a full factorial design followed by a central composite design. The analyses were performed by gas chromatography coupled with mass spectrometry. The optimized conditions of the method were three extractions using 4.0 ml of acetonitrile, with ultrasonication for 34 min. The proposed method presented good linearity (r > 0.990) and acceptable precision for low (100 ng ml−1, RSD: 1–16%), medium (300 ng ml−1, RSD: 1–19%), and high (500 ng ml−1, RSD: 2–16%) concentrations of PAHs. The limits of quantification for different PAHs ranged from 10 to 50 ng ml−1, which were suitable for atmospheric PM. Assessment of the method using sample matrix spiking/recovery assays, as well as use of a reference method, showed good recoveries for levoglucosan and for most of the PAHs and their derivatives, except for the most volatile compounds, which were lost during the evaporation of the solvent. The results for PM samples extracted by the optimized method and the reference method were in good agreement. The proposed method required 97% less solvent than the reference method, shortened the analysis time by 85%, and proved to be accurate and precise for the determination of at least 27 PAHs and their derivatives present in PM samples collected with a low-volume sampler.

Monitoring of Polycyclic Aromatic Hydrocarbon Levels in Mussels (Mytilus galloprovincialis) from Aquaculture Farms in Central Macedonia Region, Greece, Using Gas Chromatography-Tandem Mass Spectrometry Method.

A new sensitive and selective gas chromatography tandem mass spectrometry (GC-MS/MS) method was developed for the analysis of 26 polycyclic aromatic hydrocarbons (PAHs), including 16 Environmental Protection Agency (EPA) and 15 + 1 European Union (EU) PAHs, in mussel samples from aquaculture farms in Thermaikos and Strymonian Gulf, Central Macedonia Region, in three sampling periods. Concentrations were found at moderate to low values at all sampling sites, without exceeding maximum levels set by EU. Low molecular weight PAHs were predominant in all samples. Seasonal variation of the concentrations was observed; values were slightly higher in the winter period. Use of diagnostic ratios for potential sources of PAHs showed both petrogenic and pyrolitic origin. In comparison to other related studies of mussels from the Mediterranean Sea, Greek mussels cultivated in the studied gulfs are low in contaminants due to minimal environmental pollution effects. Low concentrations of PAHs are in compliance with the low values of other POPs which were found in the mussels.

Accumulation of polycyclic aromatic hydrocarbons in the devitalized aquatic moss Fontinalis antipyretica: From laboratory to field conditions.

This work aims to test the feasibility of a Fontinalis antipyretica devitalized moss clone to uptake and accumulate polycyclic aromatic hydrocarbons (PAHs) from surface waters. To assess the capability of the devitalized clone to accumulate PAHs, in the laboratory, moss was placed in water and spiked with increasing concentrations of 16 PAHs, and under field conditions, the moss was transplanted to 22 sites of Galicia (Spain) rivers. In general, PAH concentrations in water samples were lower than the maximum allowable concentrations from Directive 2013/39/EU, so the sampling sites did not show water PAH contamination. The exponential accumulation kinetic in the laboratory trial highlights a good capability of the devitalized moss clone to accumulate total PAHs. In field experiments, the hydrogeological conditions and the low emission sources caused low concentrations of PAHs in the water system and, consequently, in the transplants, although an enrichment can be observed for several PAHs. Overall, the devitalized clone of F. antipyretica can uptake and accumulate PAHs in water and may be useful in bioremediation strategies.

Sources and composition of chemical pollution in Maritime Antarctica (King George Island), part 2: Organic and inorganic chemicals in snow cover at the Warszawa Icefield

The study area is located on King George Island, where 90% of the area is permanently glaciated. This study provides a comprehensive analysis of the inorganic and organic chemistry of snow cover in the icefield and a comparison against previous results obtained in fresh water. Snow samples were collected in the summer of 2017 in the Warszawa Icefield area. Sampling points are located along two transects: between the Arctowski Polish Polar Station and the Carlini Base (N = 4), and from the forefield to the upper part of Ecology Glacier (N = 5). In the snow samples, (1) basic ions, (2) major trace metals and metalloids (and B), and (3) polycyclic aromatic hydrocarbons (PAHs) were detected and quantified. Additionally, the parameters of pH, specific electrolytic conductivity (SEC25) and total organic carbon (TOC) were determined. The results show a low concentration of inorganic elements (<30 mg/L), TOC (<1 mg/L) and PAHs (0.11–1.4 ng/L) in collected snow samples. A slight increase in PAHs and heavy-metals concentration has been observed at the marginal parts of the icefield, which suggests the impact of scientific stations. Based on this result there is a need to conduct research on pollutant levels in ice cores on King George Island to assess the risk associated with rapid glacier thawing and pollution remobilisation.

Small-scale distributions of polycyclic aromatic hydrocarbons in urban areas using geospatial modeling: A case study using the moss Orthotrichum lyellii in Portland, Oregon, U.S.A.

Polycyclic aromatic hydrocarbons (PAHs) are widespread pollutants that are costly to measure with air quality instruments. We used a spatially balanced sample of an epiphytic moss, Orthotrichum lyellii, to develop fine-scale maps of atmospheric PAHs across residential areas of Portland, Oregon. The unusual abundance of this stress-tolerant species enabled us to systematically collect a large sample (n = 350) on a 1 × 1km grid across the city. This provided the unique opportunity to investigate potential effects of more than 20 factors on PAH concentrations in moss, including emissions sources, tree canopy cover, relative elevation, short-term weather, and nuance of sample collection. We measured 20 PAHs in moss samples and assigned them to 4 groups for analysis based on molecular weight (MW): the Naphthalene, Low, Medium, and High MW groups. Spatial regression models explained a modest amount of variation in PAH concentrations in moss, with spatial structure increasing as MW increased. Motor vehicle emissions were the only PAH source we detected and was highly significant in all models. Deciduous tree cover correlated with lower PAH concentrations in moss for all except the high MW group. Short-term weather and nuance of sample collection, like height on the sampled tree, tree taxonomic family, and whether sample was primarily collected from a branch or bole, had surprisingly large effects on all groups. Overall, results aligned with expectations based on each group's dispersal potential due to MW. All PAH groups were highest over downtown Portland, along major highways, and lowest in parks and outer neighborhoods, although the details varied. Our results supported two common themes in studies directly measuring PAHs: the importance of roads as an emissions source in residential areas, and the potential for trees to reduce atmospheric concentrations. Moreover, the large effects of weather and sampling nuance have critical implications for the design of future studies.

Green Miniaturized Extraction and Microextraction of Polycyclic Aromatic Hydrocarbons from Foods and Beverages

Background: Polycyclic aromatic hydrocarbons (PAHs) are common environmental contaminants consisting of two or more fused benzene rings. PAHs can be introduced into foodstuffs through different ways, such as smoking, roasting and grilling for meat and fish, absorption from the environment for edible oils, chemical treatment of crops for plant-based products, or contamination through packaging during storage. Due to the low concentrations of PAHs in foodstuffs, a clean-up and preconcentration sample preparation technique is of high importance. Until recently, solid-phase and liquid-liquid extraction were the most popular sample preparation techniques for the extraction of PAHs from food matrices. However, due to the fundamental drawbacks of those extraction procedures, a plethora of novel methods, including micro-extraction techniques and miniaturized extraction techniques, have been developed. Moreover, a wide variety of novel adsorbent materials (e.g., metal-organic frameworks, carbon-based materials, etc.) have been synthesized and applied for PAHs’ extraction. Objective: This review aims to discuss recent advances in the extraction techniques of PAHs from food samples, utilizing novel sample preparation approaches and adsorbents. Conclusion: Compared with the traditional sample preparation techniques, the herein discussed green miniaturized extraction and microextraction techniques offer multiple benefits, including simplicity, reduced sample preparation time, as well as reduced consumption of organic solvents.

Anthropogenic and natural inputs of polycyclic aromatic hydrocarbons in the sediment of three coastal systems of the Brazilian Amazon.

Polycyclic aromatic hydrocarbons (PAHs) were measured in 32 surface sediment samples collected around three cities (Barcarena, Belém, and Santana) located on the coast of the Brazilian Amazon. The concentration of total PAHs ranged from lower than detection limit to 33,101 ng g-1 in a sample from Barcarena and was related to a large aluminum industrial complex and port activities. In Belém, which is the most populated area in the Amazon region, PAHs were probably derived from untreated sewage discharge and inputs from a large municipal landfill. Pyrogenic PAHs were predominant in both cities, with a smaller contribution of petrogenic PAHs. Low alkylated PAH levels may be associated with small boats and ship traffic. Santana had low total PAH concentrations, with a predominance of unusual alkylated PAHs, probably related to diagenetic transformations of organic matter in the sediment. In general, PAH concentrations in the samples were low and may reflect baseline levels for this Amazon estuarine system.