Transport Of Polycyclic Aromatic Hydrocarbons Research Articles

Characteristics and ecological risk assessment of polycyclic aromatic hydrocarbons in soil seepage water in karst terrains, southwest China.

Concentrations of polycyclic aromatic hydrocarbons (PAHs) in soils and soil seepage waters were analyzed along with dissolved organic carbon (DOC) to investigate the ecological risks and factors controlling the subsurface transport of PAHs in karst terrain in southwest China. The concentrations of dissolved PAHs in soil seepage water increased with depth and the mean concentrations at a depth of 80cm were relatively high (exceeding 1147ng/L). PAH composition in soil seepage water was dominated by low molecular weight (LMW) PAHs, whereas those associated with soil matrix were dominated by high molecular weight (HMW) PAHs. The results revealed that HMW PAHs in soil seepage water were closer to the equilibrium of dissolution than LMW and medium molecular weight (MMW) PAHs. However, due to the carrier functions of dissolved organic matter (DOM) for HMW PAHs, all PAHs can be continuously dissolved in the soil seepage water from soil matrix as the water moved vertical downward through the profiles. During this process, dynamic sorption and desorption processes were occurring between constituents in the soil seepage water and the soil matrix. This study demonstrates soil seepage water has posed a high risk to the groundwater, and effective protection is urgently needed.

Role of aquifer media in determining the fate of polycyclic aromatic hydrocarbons in the natural water and sediments along the lower Ganges river basin

Groundwater-sourced drinking water quality in South Asia, specifically India, is extremely stressed, mostly from the presence of many pervasive and geogenic pollutants. The presence and behavior of anthropogenic pollutants like polycyclic aromatic hydrocarbons (PAHs) are poorly investigated on a regional or basin-wide scale. The present study provides one of the first documentation of the presence and behavior of PAH in the aquifer sediments in the Ganges river basin. Lower and medium molecular weight PAHs, e.g., naphthalene, phenanthrene, and fluoranthene were detected in 79, 36, and 13% of samples (n = 25). The PAH level in groundwater was approximately five times lower than river water. The sorption behavior of PAHs were studied in experiments in presence/absence of organic carbon and by simulating advective transport of low to medium molecular weight PAHs, e.g., naphthalene, phenanthrene, and fluoranthene in aquifer sediments collected from agricultural, peri-urban, and urban areas. Naphthalene and phenanthrene adsorbed on quartz and kaolinite, but not on clay minerals like kaolinite. Fluoranthene adsorbed more favorably on kaolinite. Numerical modeling of the advective transport of PAHs in aquifers suggest up to 25 times faster movement of pollutants from irrigation-induced pumping, indicating the strong control of hydraulics on the spatial distribution of PAHs in subsurface.

Enrichment behavior of contemporary PAHs and legacy PCBs at the sea-surface microlayer in harbor water.

Polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) in the sea-surface microlayer (SML) and sub-surface water (SSW) were analyzed in and around Kaohsiung Harbor. The results confirm SML enrichments for PAHs, but PCBs less significantly, since PAHs are still produced while PCBs had banned years ago. However, PCBs still leak to the environment from contaminated sites. The results showed the sources and transport of PAHs and PCBs were different, but both are enriched in the SML. Total particulate PAHs at most sites are below the toxicity thresholds, with a few individual PAHs between the effects range-low and effect range-median even higher than the effect range-median. Total particulate PCBs might cause occasionally adverse effects in sensitive species and pose a risk to the organisms. The particulate phase in the SML poses a higher risk to the marine ecosystem than in the SSW although not all organisms will make direct use of the microlayer. Principal component analysis (PCA) of PAHs indicated the important contribution of traffic engine emission in the particulate samples of the SML and SSW and revealed that probably the petroleum pollutants are a predominant source for the dissolved phase. Cluster analysis revealed that PAH-PCB patterns in the river and anchorage channels were different to those in the wetlands and open harbor. However, PCA of PCBs showed differences in the congener profiles for the two phases, with highly chlorinated PCBs more abundant in particles, while less chlorinated PCBs were more abundant in dissolved.

Transmembrane transport of polycyclic aromatic hydrocarbons by bacteria and functional regulation of membrane proteins

In recent years, increasing research has been conducted on transmembrane transport processes and the mechanisms behind the microbial breakdown of polycyclic aromatic hydrocarbons (PAHs), including the role of membrane proteins in transmembrane transport and the mode of transmission. This article explains the adsorption, uptake and transmembrane transport of PAHs by bacteria, the regulation of membrane protein function during the transmembrane transport. There are three different regulation mechanisms for uptake, depending on the state and size of the oil droplets relative to the size of the microbial cells, which are (i) direct adhesion, (ii) emulsification and pseudosolubilization, and (iii) interfacial uptake. Furthermore, two main transmembrane transport modes are introduced, which are (i) active transport and (ii) passive uptake and active efflux mechanism. Meanwhile, introduce the proteomics and single cell analysis technology used to address these areas of research, such as Isobaric tags for relative and absolute quantitation (iTRAQ) technology and Nano Secondary ion mass spectrometry (Nano-SIMS). Additionally, analyze the changes in morphology and structure and the characteristics of microbial cell membranes in the process of transmembrane transport. Finally, recognize the microscopic mechanism of PAHs biodegradation in terms of cell and membrane proteins are of great theoretical and practical significance for understanding the factors that influence the efficient degradation of PAHs contaminants in soil and for remediating the PAHs contamination in this area with biotechnology.

The ecological impact of mineral exploitation in the Russian Arctic: A field-scale study of polycyclic aromatic hydrocarbons (PAHs) in permafrost-affected soils and lichens of the Yamal-Nenets autonomous region

Forty soil and lichen samples and sixteen soil horizon samples were collected in the mining and surrounding areas of the Yamal-Nenets autonomous region (Russian Arctic). The positive matrix factorization (PMF) model was used for the source identification of PAHs. The results of the source identification showed that the mining activity was the major source of PAHs in the area, and that the mining influenced the surrounding natural area. The 5+6-ring PAHs were most abundant in the mining area. The lichen/soil (L/S) results showed that 2+3-ring and 4-ring PAHs could be transported by air and accumulated more in lichens than in the soil, while 5+6-ring PAHs accumulated more in the soil. Strong relationships between the quotient of soil/lichen (QSL) and Log KOA and Log PL and between the quotient of lichen/histic horizon soil and KOW were observed. In addition, hydrogeological conditions influenced the downward transport of PAHs. Particularly surprising is the discovery of the high levels of 5 + 6 rings in the permafrost table (the bottom of the active layer). One hypothesis is given that the global climate change may lead to further depth of active layer so that PAHs may migrate to the deeper permafrost. In the impact area of mining activities, the soil inventory for 5+6-ring PAHs was estimated at 0.14 ± 0.017 tons on average.

Soil heterogeneity and surfactant desorption influence PAH distribution during electroremediation at a tar oil-contaminated site.

After a field experiment utilising electroosmosis and non-ionic surfactant Tween 80 as a remediation effort on the removal of polycyclic aromatic hydrocarbons (PAHs) from a long-term asphalt-contaminated soil, the PAH heterogeneity in the soil was yet extensive. This study come as a follow-up to address the following questions: (i) was PAH (re)distribution a consequence of the treatment? and (ii) to what extent does the surfactant affected PAH desorption and subsequent bioavailability? To answer question (i), we selected random soil samples from different locations of the field site before in situ remediation took place, and quantified and characterised soil organic matter by elemental analysis and solid-phase 13C nuclear magnetic resonance spectroscopy and PAH concentrations. Finally, batch desorption experiments with selected contaminated soil samples were carried out with and without 1% Tween 80 in the solution phase to address question (ii). Data shows that PAH concentrations were related neither to organic matter content nor to a high aromaticity of the organic matter, which serves as a proxy for the presence of tar oil. Soil heterogeneity is likely to be the cause of PAH heterogeneous distribution, but it is inferred that remediation causes weathering of the tar oil phase, resulting in the release and subsequent transport and sorption of PAH to inherent organic material. The results of the batch desorption experiments demonstrate PAH desorption up to 146 times when surfactant is present. However, Tween 80 does not enable biodegradation, since desorbed PAH molecules are entrapped inside surfactant micelles.

Influence of sediment parameters on the distribution and fate of PAHs in an estuarine tropical region located in the Brazilian semi-arid (Jaguaribe River, Ceará coast)

18 polycyclic aromatic hydrocarbons (PAHs) were evaluated in the Jaguaribe River to explore the influence of grain size, organic carbon, humic and fulvic acids and black carbon on their adsorption onto sediment. The ∑PAHs concentrations variated from 0.6 to 3752.0 ng g−1 with highest concentrations in the estuarine zone. The PAHs predominant source along the river was from mixed sources, mainly related to biomass combustion, small oil spills related to recreational nautical activities and runoff from cities. Organic and inorganic parameters presented influence on PAHs distribution along the river, with humic acid as a determinant factor. These research findings are of importance to an assessment of the fate and transport of PAHs in estuarine systems.

Seasonal variation and spatial transport of polycyclic aromatic hydrocarbons in water of the subtropical Jiulong River watershed and estuary, Southeast China

Riverine runoff is one of the most important pathways of pollutants entering the oceans. To study the seasonal variations, spatial transports, sources and mass fluxes of polycyclic aromatic hydrocarbons (PAHs) from the subtropical Jiulong River watershed to estuary, water samples were collected in wet and dry seasons. PAH concentrations showed significant temporal-spatial variations (ANOVA, p < 0.05). In the watershed, PAH concentrations in wet season (48.6 ± 18.2 ng L−1) were significantly lower than in dry season (90.3 ± 18.5 ng L−1). In contrast, estuarine PAH concentrations in wet season (67.1 ± 24.6 ng L−1) were significantly higher than in dry season (27.4 ± 10.6 ng L−1) (p < 0.0001). The spatial variations of PAH concentrations in wet and dry seasons reflected positive and restricted transport processes occurred in the river. These findings might be subjected to seasonal changes in precipitation, water discharge, hydrodynamic conditions, and human activities. The compositional patterns of PAHs illustrated that fluorene and phenanthrene were the dominant compounds in the watershed, while phenanthrene was predominant in the estuary. Source analysis by molecular diagnostic ratios and PMF model indicated that fossil fuel and biomass combustion and petroleum both contributed to the presence of PAHs, and the high contributions of pyrogenic PAHs might be related to urban rainstorm runoff in winter and atmospheric inputs in winter. Although the estimated flux of PAHs from watershed to estuary was about 676 kg yr−1 with a low level by comparing the data obtained in the worldwide, continue concern of PAHs in the Jiulong River is recommended due to the intense human activities.

Multiphase reactivity of polycyclic aromatic hydrocarbons is driven by phase separation and diffusion limitations

Benzo[a]pyrene (BaP), a key polycyclic aromatic hydrocarbon (PAH) often associated with soot particles coated by organic compounds, is a known carcinogen and mutagen. When mixed with organics, the kinetics and mechanisms of chemical transformations of BaP by ozone in indoor and outdoor environments are still not fully elucidated. Using direct analysis in real-time mass spectrometry (DART-MS), kinetics studies of the ozonolysis of BaP in thin films exhibited fast initial loss of BaP followed by a slower decay at long exposure times. Kinetic multilayer modeling demonstrates that the slow decay of BaP over long times can be simulated if there is slow diffusion of BaP from the film interior to the surface, resolving long-standing unresolved observations of incomplete PAH decay upon prolonged ozone exposure. Phase separation drives the slow diffusion time scales in multicomponent systems. Specifically, thermodynamic modeling predicts that BaP phase separates from secondary organic aerosol material so that the BaP-rich layer at the surface shields the inner BaP from ozone. Also, BaP is miscible with organic oils such as squalane, linoleic acid, and cooking oil, but its oxidation products are virtually immiscible, resulting in the formation of a viscous surface crust that hinders diffusion of BaP from the film interior to the surface. These findings imply that phase separation and slow diffusion significantly prolong the chemical lifetime of PAHs, affecting long-range transport of PAHs in the atmosphere and their fates in indoor environments.

Environmental effects on the bioaccumulation of PAHs in marine zooplankton in Gaoping coastal waters, Taiwan: Concentration, distribution, profile, and sources

Polycyclic aromatic hydrocarbons (PAHs) are toxic and ubiquitous in the environment and pose great risks. Bioaccumulation by plankton is the outset for PAHs entering marine food web. The long-term driving environmental factors for bioaccumulation of PAHs in zooplankton have not been well investigated. In this study, high variation of PAH concentrations in zooplankton (5 to 5440 ng g−1 dry weight) was found, with the highest PAH levels near the transect Kaohsiung Harbor. Precipitation significantly enhances the PAH concentration in zooplankton and affects the PAH distribution in the water column, indicating PAH input from terrestrial runoff. The sources of PAHs in the coastal waters are a mixture of petroleum and combustion. Biomass dilution dominates bioaccumulation of PAHs in zooplankton, especially for the dominant species, copepods. This study provides the first information on PAH bioaccumulation in zooplankton to understand PAH transport in the plankton food web in subtropical coastal waters.

Monitoring polycyclic aromatic hydrocarbon concentrations and distributions in rice paddy soils from Gyeonggi-do, Ulsan, and Pohang

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous pollutants that are released by incomplete combustion of carbon-containing materials. The top soils of rice paddies were collected from Gyeonggi-do (18 sites), Ulsan (20 sites), and Pohang (19 sites) in Korea to assess the spatial distribution and potential sources of PAHs. The total concentrations of 15 PAHs in the soils were 19.53–672.93, 125.01–3106.27, and 51.94–8106.21 mg/kg in Gyeonggi province, Ulsan, and Pohang, respectively. The concentration of 7 key carcinogenic PAHs were followed the order: Pohang (38.54–4826.63 ng/g) > Ulsan (28.54–1561.39 ng/g) > Gyeonggi province (19.53–206.51 ng/g). Three-ring PAHs were predominant in the soils from Gyeonggi-do while 3–5 ring compounds were abundant in the agricultural soils from the two industrial regions (Ulsan and Pohang). The PAH isomeric diagnostic ratios indicated that PAH contamination in the two cities mainly originated from pyrogenic sources. The principal component analysis indicated that pyrogenic coal burning and residential biomass combustion were major contributors to the soil contamination in the two cities. The transportation of PAHs through the air from industrial complexes and high volume of traffic may influence the PAHs distribution in the soils of the two cities in Korea.

Gas–particle partition and spatial characteristics of polycyclic aromatic hydrocarbons in ambient air of a prototype coking plant

This study investigated the gas–particle partition and spatial characteristics of polycyclic aromatic hydrocarbons (PAHs) in the ambient air of a prototype coking plant. High-volume samplers with glass fiber filters (GFFs) and polyurethane foams (PUFs) were used to collect PAHs in both gaseous and particulate phases. The EPA's 16 priority-controlled PAHs were measured using gas chromatography equipped with a mass-selective detector (GC-MS). The total PAH concentrations ranged from 1.32 μg m−3 to 9.41 μg m−3, with an average of 4.20 μg m−3. PAH abundance at the various sites of the coking plant was determined to be in the following order: coke side > machine side > leeward site; the lowest values were at the reference site and factory boundary. The medium-molecular-weight PAHs had the highest fraction at the coke side, whereas the low-molecular-weight PAHs were predominant at other sampling sites. Considerable amount of chrysene was detected at the coke side, fluorene at the machine side, acenaphthene at the leeward site (240 m downwind of the coke oven), and naphthalene at the other three sites. The gaseous fractions of PAHs at the six sampling sites ranged from 46.3% to 85.8% of the total PAHs in the gas–particle systems; and gaseous PAHs were predominant in the ambient air of the coking plant—except for the coke side, where the PAHs were dominantly partitioned to the particles. In addition, the particulate benzo(a)pyrene equivalence (BaPeq) fraction was high in the coking plant air. The slope (mr) values ranged from −0.59 to −0.39 in the plant, indicating that the absorption mechanism, rather than the adsorption mechanism, dominated the gas–particle partitioning. The intercept (br) values carry the information on the gaseous–particulate phase distribution of semivolatile organic compounds when the mr values are similar. The organic matter fraction in particles, particulate phase fraction of PAHs, and toxicity of particulate matter were found to increase with an increase in br values at similar mr values. The predominant mechanism was absorption for dibenz(a,h)anthracene, benzo(ghi)perylene, and indeno(1,2,3-cd)pyrene, but adsorption for benzo(b)fluoranthene, benzo(a)pyrene, and benzo(k)fluoranthene at the coke and machine sides. By contrast, for most high-molecular-weight PAHs, absorption into the organic matter was the predominant mechanism at other sites. The gas–particle partitioning mechanism of individual PAHs was closely related to the distance from the coke oven, rather than the orientation to the oven. These results may be of great importance in understanding the pollutant process and atmospheric transport of PAHs and may provide guidance to decision makers regarding air pollution control.

Distribution of polycyclic aromatic hydrocarbons (PAHs) from legacy spills at an Alaskan Arctic site underlain by permafrost

Widespread polycyclic aromatic hydrocarbon (PAH) contamination resulting from petroleum spills at military and industrial sites along the Arctic Ocean Coast is a major issue in the Alaskan Arctic. Polycyclic aromatic hydrocarbons (PAHs) consist of one or more fused aromatic rings and comprise a major portion of petroleum products like fuels. PAHs are commonly found in a variety of geomedia and are considered environmentally persistent, toxic, and carcinogenic. In the present study, the subsurface distribution of PAHs was investigated at a former U.S. Department of the Navy site in northern Alaska using laser-induced fluorescence coupled with ultraviolet optical screening tool (LIF-UVOST). The former Naval Arctic Research Laboratory (NARL) study site has historical presence just outside the city of Utqiaġvik, Alaska (formerly Barrow) and has a long history of petroleum spills since the early 1950s primarily at the Airstrip and Powerhouse sites. To determine the extent of PAH accumulation in the subsurface a total of 143 vertical soil profiles were characterized using LIF-UVOST during September 2015 (87 at the Airstrip site and 56 at the Powerhouse site). We also compared the intensities of different wavelengths (350 versus 500 nm) to estimate spill source and we found a substantial accumulation of PAHs in the surface and subsurface at both sites and vertical distribution of PAHs was primarily heterogeneous, varying as a function of probing locations and soil depth. Both sites were found to have no correlation between depth of the maximum fluorescence signal and depth of the probing refusal depth (top of permafrost). Using LIF-UVOST for the direct chemical sensing of PAHs proved to be a useful tool and revealed unique signature PAH fluorescence responses when comparing 350 and 500 nm intensities between the Airstrip and Powerhouse sites, likely attributable to the original source of the spill. Results from this project can be directly used for other potential studies, including planning remediation strategies and investigating local bodies of water for PAH transport.

Integrating organic chemical simulation module into SWAT model with application for PAHs simulation in Athabasca oil sands region, Western Canada

An integrated watershed model is a key tool for assessing the fate and transport of organic chemicals. We developed and integrated an organic chemical simulation module into Soil Water Assessment Tool (SWAT) model and used it for Polycyclic Aromatic Hydrocarbons (PAHs) simulation in Muskeg River Watershed in Athabasca oil sands region, Western Canada. The model uses a three-phase partition process to simulate the chemicals partitioning to Dissolved Organic Carbon (DOC) in both soil water and streams. The simulation performances for Phenanthrene and Pyrene loads for a period of 2015–2017 were assessed to be of ‘satisfactory’ quality. The model simulation results indicated that the summer season is the hot moment and the rainfall-runoff event is the driving force for the PAHs transport in the watershed. The developed simulation module could be a useful modeling tool to simulate and asess the pathway, fate and transport of organic chemicals at the watershed scale.

A multimedia fugacity model to estimate the fate and transport of polycyclic aromatic hydrocarbons (PAHs) in a largely urbanized area, Shanghai, China

Increasing PAHs pollution is creating more complex urban pollution system. However, the availability of sufficient monitoring activities for PAHs in multicompartment and corresponding multi-interface migration processes is still not well understood. In this study, a Level III steady state fugacity model was validated to evaluate the detailed local variations, and mass fluxes of PAHs in various environmental compartments (i.e., air, soil, sediment, water, vegetation and organic film). This model was applied to a region of Shanghai in 2012 based on a large number of measured data and brings model predictions in 2020. The model results indicate that most of the simulated concentrations agreed with the observed values within one order of magnitude with a tendency of underestimation for vegetation. Direct emission is the main input pathway of PAHs entering the atmosphere, whereas advection is the main outward flow from Shanghai. Organic film was achieved the highest concentration of PAHs compared to other compartments up to 58.17 g/m3. The soil and sediment served as the greatest sinks of PAHs and have the longest retention time (2421.95–78642.09 h). Importantly, a decreasing trend of PAHs was observed in multimedia from 2012 to 2020 and the transfer flux from the air to vegetation to soil was the dominant pathways of BaP intermedia circulation processes. A sensitivity analysis showed that temperature was the most influential parameter, especially for Phe. A Monte Carlo simulation emphasized heavier PAHs were overpredicted in film and sediment, but lighter PAHs in air and water were generally underestimated.

Assessing the level and sources of Polycyclic Aromatic Hydrocarbons (PAHs) in soil and sediments along Jhelum riverine system of lesser Himalayan region of Pakistan

Lesser Himalayan Region (LHR) is an important mountain ecosystem which supports a wide range of biodiversity for native flora and fauna. Human population in this region is largely dependent upon local sources for their livelihood. Surface soil (n = 32) and sediment (n = 32) were collected from four different altitudinal ranges of LHR and analyzed for priority Polycyclic Aromatic Hydrocarbons (PAHs) recommended by USEPA. Level, sources and distribution pattern of PAHs were assessed in soil and sediments samples collected from four altitudinal zones in LHR. Total PAHs concentration level of PAHs in soil and sediments ranged from 62.79 to 1080 ng g−1 and 14.54–437.43 ng g−1, respectively. Compositional profile of PAHs in both soil and sediment were dominated by low and medium molecular weight PAHs, ranged from 18.02 to 402.18 ng g−1in soil and 0.32–96.34 ng g−1in sediments. In the context of spatial distribution trend, highest mean concentrations of PAHs in soil were recorded in zone D (sites from the rural region) and for sediments highest concentrations were detected at zone A, which includes dam sites. In all four zones, no altitudinal trend of PAHs in soil and sediments was observed. Source apportionment through receptor modelling by positive matrix factorization (PMF) revealed that local sources such as biomass combustion and vehicular emissions are important sources of PAHs in this region. The prevalence of monsoon atmospheric circulation system in LHR implicated that this region is also influenced by medium and long range atmospheric transportation of PAHs from neighboring countries where potential sources and high level of PAHs has been reported.

Transport of polycyclic aromatic hydrocarbons in a highly vulnerable karst underground river system of southwest China.

The concentration and fluxes of polycyclic aromatic hydrocarbons (PAHs) were investigated in a karst underground river system in southwest China. Groundwater, particles, and sediments from underground river, topsoil, and surface water were monitored, allowing establishment of a conceptual model of PAH transport at the watershed scale. The results showed that PAHs could be transported from the surface to the subsurface through two migration pathways, which were slow-flowing water in the karst fissure and fast-flowing water in conduits. During rainfall events, increasing PAH levels (concentrations and fluxes) at the underground river exit indicated that hydrodynamic force could facilitate PAH transport. The PAHs in water were dominated by dissolved PAHs, accounting for 58.7% of total, especially in the freely dissolved phase, in which SPM-associated PAHs accounted for 41.3% of the total PAHs. Low molecular weight PAHs dominated transport and were mainly transported in dissolved form, whereas high molecular weight PAHs were dominated by SPM-associated transport during the rainfall events. A significantly positive correlation was observed between two-ring and three-ring freely dissolved PAHs and dissolved organic carbon (p < 0.01), respectively. Moreover, PAHs with four to five rings were relatively more abundant in the dissolved organic matter (DOM) associated phase than in the freely dissolved phase, suggesting a major role of DOM in their transport during rainfall events. The trend of PAH fluxes suggested that particle-facilitated transport was another dominant cause of PAH mobilization.

The effects of dredging and environmental conditions on concentrations of polycyclic aromatic hydrocarbons in the water column

Sediment dredging can cause damage to the marine environment due to mobilization of sediments and contaminants. The effects of dredging and boundary environmental conditions on the concentration of Polycyclic Aromatic Hydrocarbons (PAHs) in water were evaluated during dredging of the Oil Port of Genoa-Multedo (Italy). Results showed that turbidity and PAH concentrations increased in the water during dredging. However, the scenario was complex due to the high number of interacting physical-chemical factors influencing PAH concentrations and transport. Due to these, PAH distribution is different in water, where low-molecular-weight PAHs were predominant (maximum concentration 0.105 μg L−1), and in bottom sediments, where high-molecular-weight PAHs had the highest concentrations (from 299.3 to 1256.5 ng g−1). Moreover, mainly during dredging the PAH concentrations in water were significantly higher inside than outside the port as a consequence of the lower dynamics within the port basin. Turbidity was the main parameter related to PAH concentrations.

GEM-MACH-PAH (rev2488): a new high-resolution chemical transport model for North American polycyclic aromatic hydrocarbons and benzene

Abstract. Environment and Climate Change Canada's online air quality forecasting model, GEM-MACH, was extended to simulate atmospheric concentrations of benzene and seven polycyclic aromatic hydrocarbons (PAHs): phenanthrene, anthracene, fluoranthene, pyrene, benz(a)anthracene, chrysene, and benzo(a)pyrene. In the expanded model, benzene and PAHs are emitted from major point, area, and mobile sources, with emissions based on recent emission factors. Modelled PAHs undergo gas–particle partitioning (whereas benzene is only in the gas phase), atmospheric transport, oxidation, cloud processing, and dry and wet deposition. To represent PAH gas–particle partitioning, the Dachs–Eisenreich scheme was used, and we have improved gas–particle partitioning parameters based on an empirical analysis to get significantly better gas–particle partitioning results than the previous North American PAH model, AURAMS-PAH. Added process parametrizations include the particle phase benzo(a)pyrene reaction with ozone via the Kwamena scheme and gas-phase scavenging of PAHs by snow via vapour sorption to the snow surface. The resulting GEM-MACH-PAH model was used to generate the first online model simulations of PAH emissions, transport, chemical transformation, and deposition for a high-resolution domain (2.5 km grid cell spacing) in North America, centred on the PAH data-rich region of southern Ontario, Canada and the northeastern US. Model output for two seasons was compared to measurements from three monitoring networks spanning Canada and the US Average spring–summertime model results were found to be statistically unbiased from measurements of benzene and all seven PAHs. The same was true for the fall–winter seasonal mean, except for benzo(a)pyrene, which had a statistically significant positive bias. We present evidence that the benzo(a)pyrene results may be ameliorated via further improvements to particulate matter and oxidant processes and transport. Our analysis focused on four key components to the prediction of atmospheric PAH levels: spatial variability, sensitivity to mobile emissions, gas–particle partitioning, and wet deposition. Spatial variability of PAHs ∕ PM2.5 at a 2.5 km resolution was found to be comparable to measurements. Predicted ambient surface concentrations of benzene and the PAHs were found to be critically dependent on mobile emission factors, indicating the mobile emissions sector has a significant influence on ambient PAH levels in the study region. PAH wet deposition was overestimated due to additive precipitation biases in the model and the measurements. Our overall performance evaluation suggests that GEM-MACH-PAH can provide seasonal estimates for benzene and PAHs and is suitable for emissions scenario simulations.

Dynamics of polycyclic aromatic hydrocarbons (PAHs) in water column of Pearl River estuary (China): Seasonal pattern, environmental fate and source implication

Based on a monthly sampling effort in 2011, >62 polycyclic aromatic hydrocarbons (PAHs) in different environmental phases were detected in the Pearl River estuary, China. The study aimed to investigate seasonal variation in PAH concentration and composition, potential risk source, depth profile and environmental correlation and to provide a non-deterministic insight into the PAH behavior. The total PAHs varied widely throughout the 12 months of the study period, ranging from 25.99 ng/l to 522.26 ng/l in seawater and from 7.37 μg/g to 167.44 μg/g in suspended sediment (SPM). The 16 Environmental Protection Agency (EPA) priority PAHs ranged from 12.70 ng/l to 160.15 ng/l in seawater and from 2.82 μg/g to 112.32 μg/g in SPM. Low molecular weight (LMW) PAHs (2- and 3-ring) were the most abundant, responsible for 81% in seawater and 73% in SPM. Moreover, it appeared that SPM and ambient water temperature were the determining factors controlling the transport and distribution of PAHs in the water column. A higher concentration of SPM contributed to a higher content of PAHs due to adsorption and low solubility. The PAHs were more significantly associated with particles than were dissolved in seawater. In addition, petroleum emissions, vehicle emissions, and wood combustion were considered a potential risk of PAHs via statistically-based methods of principal component analysis (PCA) and diagnostic ratios. The findings are useful for understanding the dynamics of estuarine PAHs, which exert significant influence on coastal ecosystems.