Transport Of Polycyclic Aromatic Hydrocarbons Research Articles

Sediment organic matter predicts polycyclic aromatic hydrocarbon distribution in port sediments

We evaluated the influence of organic matter in polycyclic aromatic hydrocarbons (PAHs) in port sediments using multiple linear regression (MLR) and prediction models. Total sediment PAHs ranged between 45 and 3230 ng/g dw (average: 557 ± 962 ng/g dw), with PAHs primarily originating from river inputs, confined to areas near the estuaries. Coal/biomaterial combustion and petroleum mainly contribute to the presence of PAHs along estuaries, with medium-high to high ecological risks. MLR TPAHs prediction model included variables, namely, the marine-derived total organic carbon (TOCmar), terrestrial fraction of organic matter (Fterr), and carbon-to‑nitrogen ratio (CNR). Results indicate that mainly marine- followed by terrestrially-derived organic matter influenced sediment PAH distribution. Total organic nitrogen and CNR were variables in the toxic equivalent (TEQ) prediction model, demonstrating that terrestrial pollution sources primarily influenced TEQ. The study analyzes and predicts the impact of organic matter and its sources on the fate and transport of PAHs in port sediments.

Seasonal dynamics of polycyclic aromatic hydrocarbons in microplankton from Kaohsiung Harbor (Taiwan Strait, northeastern South China Sea)

The impact of polycyclic aromatic hydrocarbons (PAHs) on the marine food web is crucially understudied in the primary trophic system. We evaluated the seasonal dynamics of PAHs in microplankton in a polluted environment (Taiwan), northeastern South China Sea. Replicate size-fractionated microplankton (55–1000 μm) were freeze-dried, and PAHs were extracted with a 1:1 v/v ratio of acetone: n-hexane, then analyzed using GC–MS. Total PAHs ranged between 68 and 2548 ng/g dw in microplankton, greatest during spring (130–2548 ng/g), followed by autumn (135–772 ng/g) and summer (44–423 ng/g). Spatial distribution varied through seasons but was higher in the southern part (S6 > S4 > S5 > S2 > S3 > S1 > S7), dominated by higher-ring PAHs from mixed pyrogenic and petrogenic sources. PAHs are significantly correlated with environmental factors, especially in colder seasons and lower salinity areas. Suspended matter and plankton influenced PAH transport and partitioning seasonally. Plankton's PAHs seasonal changes and environmental influences are revealed in an anthropic environment.

Long-Range Transport of Polycyclic Aromatic Hydrocarbons and Metals in High Altitude Lacustrine Environments of the Eastern Himalayas: Speciation, and Source Apportionment Perspectives

Long-Range Transport of Polycyclic Aromatic Hydrocarbons and Metals in High Altitude Lacustrine Environments of the Eastern Himalayas: Speciation, and Source Apportionment Perspectives

Indole-3-acetic acid enhances the co-transport of proton and phenanthrene mediated by TaSAUR80-5A in wheat roots

Polycyclic aromatic hydrocarbons (PAHs) are a type of organic pollution that can accumulate in crops and hazard human health. This study used phenanthrene (PHE) as a model PAH and employed hydroponic experiments to illustrate the role of indole-3-acetic acid (IAA) in the regulation of PHE accumulation in wheat roots. At optimal concentrations, wheat roots treated with PHE + IAA showed a 46.9% increase in PHE concentration, whereas treatment with PHE + P-chlorophenoxyisobutyric acid resulted in a 38.77% reduction. Transcriptome analysis identified TaSAUR80-5A as the crucial gene for IAA-enhancing PHE uptake. IAA increases plasma membrane H+-ATPase activity, promoting active transport of PHE via the PHE/H+ cotransport mechanism. These results provide not only the theoretical basis necessary to better understand the function of IAA in PAHs uptake and transport by staple crops, but also a strategy for controlling PAHs accumulation in staple crops and enhancing phytoremediation of PAH-contaminated environments.

Climate change and human impacts on aquatic communities at Etoliko Lagoon in western Greece

The Etoliko Lagoon in western Greece has experienced extensive human modification since the 20th century, both on the surrounding land and in the aquatic environment. To examine human impacts and disentangle climatic from anthropogenic changes, we present a suite of biomarker records that span the past two centuries (∼1790–2011). Specifically, we use terrigenous (n-alkanes, polycyclic aromatic hydrocarbons (PAHs), and phytosterols) and aquatic (dinosterol, brassicasterol, cholesterol, and stigmasterol) biomarkers to document changes in nutrient inputs, combustion, and algal productivity. During most of the 19th and 20th centuries, aquatic communities respond to temperature, forced mainly by solar irradiance and volcanic activity, and precipitation, controlled largely by summer and winter North Atlantic Oscillation (NAO) patterns that determine freshwater runoff. PAHs illustrate the acceleration of coal combustion during the 1800s, and declining concentrations since the 1950s correspond to the implementation of emission controls and reductions in rainfall that likely inhibited PAH transport. As human pressures increased in the late 1900s and water column anoxia grew, the absence of a clear human waste and eutrophication signal suggests that other factors also contributed to limited oxygen availability. Overall, environmental degradation of the late 20th and early 21st centuries is clear and can be attributed to a combination of especially arid conditions and human interferences that altered lagoon hydrography, trophic state, and aquatic community composition.

Systematic underestimation of polycyclic aromatic hydrocarbon aqueous concentrations in rivers

Polycyclic aromatic hydrocarbons (PAHs) are a widespread group of organic contaminants whose presence in water bodies is cause of severe concern. With few exceptions, the majority of PAHs is hydrophobic, presents a high adsorption affinity, and is thus primarily transported within river systems during high-flow events together with suspended particulate matter (SPM). Evidence exists of analytical challenges related to the incomplete extraction of PAHs adsorbed to solids and thus to a potential negative bias in the chemical analysis of PAHs in bulk water samples with high SPM content. Despite this, partly due to the elevated efforts required to collect representative samples containing sufficient SPM for the separate PAH analysis in this matrix, several investigations rely on the analysis of aqueous samples. This study tests the hypothesis that surveys based exclusively on bulk water may lead to a systematic underestimation of the real contamination level and transport of PAHs in rivers. Six high-turbidity events were examined in three Austrian rivers applying time-integrated sampling and simultaneously analyzing PAHs in total bulk water, filtered water, SPM, and supernatant. Despite an unavoidable degree of uncertainty in such challenging sampling scheme, the results indicate that measurements performed with best available standard methods in bulk water samples determined in average only about 40% of the theoretically expected total PAHs concentrations derived from the analyses in SPM. Such deviation has important implications for the reliable assessment of the compliance with environmental quality standards as well as for surveys aimed to estimate riverine loads, validate emission models, and understand the transport dynamics of PAHs in rivers. Whereas the first objective, e.g., in European countries, is alternatively achieved via monitoring in biota, the latter ones require efforts directed to complement monitoring campaigns with separate sampling of SPM, with monitoring of suspended solids transport to appropriately select and interpret the results of water samples and to improve the chemical analysis of PAHs in bulk water samples with high solids content.

Simulation and parameter determination of the net sorption of phenanthrene by sediment particles

The distribution of polycyclic aromatic hydrocarbons (PAHs) in the ocean is affected by the sorption-desorption process of sediment particles. This process is determined by the concentration of PAHs in seawater, water temperature, and organic matter content of sediment particles. Quantitative relationships between the net sorption rates (=the difference of sorption and desorption rates) and these factors have not been established yet and used in PAH transport models. In this study, phenanthrene was chosen as the representative of PAHs. Three groups of experimental data were collected to address the dependence of the net sorption processes on the initial concentration, water temperature, and organic carbon content representing organic matter content. One-site and two-compartment mass-transfer models were tested to represent the experimental data using various parameters. The results showed that the two-compartment mass-transfer model performed better than the one-site mass-transfer model. The parameters of the two-compartment mass-transfer model include the sorption rate coefficients kafand kas (L g−1 min−1), and the desorption rate coefficients kdf and kds (min−1). The parameters at different temperatures and organic carbon contents were obtained by numerical simulations. Linear relationships were obtained between the parameters and water temperature, as well as organic carbon content. kaf, kas and kdf decreased linearly, while kds increased linearly with temperature. kaf, kas and kdf increased linearly, while kds decreased linearly with organic carbon content. The r2 values between the simulation results based on the relationships and the experimental results reached 0.96–0.99, which supports the application of the model to simulate sorption-desorption processes at different water temperatures and organic carbon contents in a realistic ocean.

Investigation of 200 anthropogenic activities in a representative alpine peatland in the Altay Mountains, northwestern China

Peatlands records can be used to reconstruct and understand the history of environmental evolution, as well as a more accurate reflection of human activities. The black carbon (BC) and polycyclic aromatic hydrocarbons (PAHs) are ideal natural archives of anthropogenic activities. To identify the information of anthropogenic activities recorded by peatlands in the middle and high latitudes of the alpine mountains in the arid and semi-arid regions of China. this study analyzed the concentrations of BC, δ13C ratios of BC, PAHs, and molecular diagnostic ratios of PHAs (including Benzo(a) anthracene (BaA), Chrysene (Chr), fluoranthene (Flt), anthracene (Ant), phenanthrene (Phe), Benzo(a) pyrene (BaP), and pyrene (Pyr) in a 30-cm peat profile from the Altay Mountain, northwestern China. Our results revealed concentrations of BC from 11.71 to 67.5 mg·g−1, and PAHs from 168.09 to 263.53 ng·g−1. The δ13CBC value ranged from − 31.37 to − 26.27‰, with an average of − 29.54‰, indicating that the BC mainly comes from biomass combustion. The ratios of BaA/(BaA + Chr), Flt/(Flt + Pyr), and Ant/(Ant + Phe) exceeded 0.35, 0.5, and 0.1, respectively, revealing that the PAHs pollutants mainly originated from the combustion of biomass and fossil fuel burning. Furthermore, based on these findings and our knowledge of social development in Altay, industrial transport and tourism have influenced the emission, transport, and deposition of BC and PAH in peatlands in the Altay mountains since the 1980s. After 1980, pollutant concentrations decreased with the implementation of environmental policies. The results not only reveal the influence of anthropogenic activities on the sedimentary characteristics of peatlands in the Altay Mountains, but also provide an important theoretical basis for the conservation of fragile mountain peatlands.

The effect of bioturbation on the release behavior of polycyclic aromatic hydrocarbons from sediments: A sediment–seawater microcosm experiment combined with a fugacity model

The effects of two benthonic species, Perinereis aibuhitensis and Matuta planipes Fabricius, on the release of polycyclic aromatic hydrocarbons (PAHs) from sediments were investigated using a sediment–seawater microcosm. A Level IV fugacity model was used to simulate the behavior and fate of PAHs in the environment. This study revealed that both benthos significantly influenced the release of PAHs, and Matuta planipes Fabricius had a stronger disturbance effect than another. The final concentrations of Matuta planipes Fabricius group, Perinereis aibuhitensis group and the control group in the seawater phase reached 10.8, 9.94 and 7.90 μg/L, respectively. There were certain differences in the behaviour of the two benthonic species. Matuta planipes Fabricius caused more sediment resuspension, while Perinereis aibuhitensis increased the total organic carbon (TOC) content in the environment. The vertical concentration distribution of sediment indicated that vertical mixing was slightly stronger in the Matuta planipes Fabricius group than that in the Perinereis aibuhitensis group. The fugacity model effectively simulated the release behavior of PAHs, providing insight into PAH transport and distribution. The results demonstrated that bioturbation could promote the release of PAHs from seawater. The amount of PAHs released was significantly correlated with the biological habits of the benthos.

Mechanism, Formation and Transport of Polycyclic Aromatic Hydrocarbons (PAHs) in Fruits, Vegetables and Fresh Fish Species in Africa: A Systematic Review of its Health Risk

Mechanism, Formation and Transport of Polycyclic Aromatic Hydrocarbons (PAHs) in Fruits, Vegetables and Fresh Fish Species in Africa: A Systematic Review of its Health Risk

Promotive effects of marine-derived dimethyl sulfoxide on the photodegradation of phenanthrene in the atmosphere

Dimethyl sulfoxide (DMSO), a versatile medium, is a particular component in the marine atmosphere that possibly causes polycyclic aromatic hydrocarbons (PAHs) to degrade differently than they do in the continental atmosphere. In this study, phenanthrene (Phe) was used as a model PAH in batch photochemical experiments to investigate the chemical actions of DMSO and the underlying mechanisms. The photodegradation of Phe in aqueous solutions with DMSO volume fractions from 0 % to 100 % was initiated by ultraviolet (UV) radiation and promoted by singlet oxygen, which was consistent with pseudo-first-order kinetics. Phe photodegraded faster in a mixture of DMSO and water than in water or DMSO alone, and the rate constant showed a unimodal distribution over the DMSO fraction range, peaking at 33 % DMSO (0.0333 ± 0.0009 min−1) and 40 % DMSO (0.0199 ± 0.0005 min−1) under 254 nm and 302 nm UV radiation, respectively. This interesting phenomenon was attributed to the competition of DMSO for UV radiation and singlet oxygen and changes in dissolved oxygen and free water contents caused by the interaction between DMSO and water molecules. In addition, 9,10-phenanthrenequinone (9,10-PhQ) with high cytotoxicity was the main photodegradation product of Phe under various conditions. The photodegradation rate of Phe in the mixtures of DMSO and water was comparable to its reaction rate with OH radicals, suggesting that 9,10-PhQ can be rapidly generated in the marine atmosphere, driven by a mechanism different from that in the continental or urban atmosphere. Under the presented experimental conditions, UV intensity and DMSO fraction were the primary factors that affected the photodegradation rate of Phe and 9,10-PhQ and altered their integrated toxicity. The findings of this study support the conclusion that the marine atmosphere is an essential field in the atmospheric transport of PAHs, in which DMSO is an important component that affects their photodegradation.

Characterization of polycyclic aromatic hydrocarbons in mangrove sediments from Ifiekporo Creek, Warri, Nigeria

The occurrence and level of polycyclic aromatic hydrocarbons (PAHs) in mangrove sediment from Ifiekporo Creek in Warri, Delta State, Nigeria, were assessed in this study. The extraction of PAHs from the sediment samples was achieved using the PAH analytical test method (USEPA 8270). This method measures the individual concentrations of extractable PAHs in samples. The PAHs were quantified within the C11-C22 subgroup. The basic GC parameters for the analysis of polyaromatic hydrocarbons were analysed using a gas chromatography‒mass selective detector (GC‒MSD). The individual PAH concentrations in the mangrove sediment samples ranged from 850 µg/kg−1 to 3470 µg/kg−1. PAH source apportionment employing isomeric ratios and multivariate statistics indicated both pyrogenic and petrogenic source inputs in the sediment samples. The order of PAH homology in the sediment was 3-ring > 2-ring > 4-ring. The sediment samples were mostly dominated by LMW PAHs. The results of the ecological risk assessment in the study area indicate that there is low ecological risk associated with PAH exposure in sediment. These results provide data on the concentrations and compositional patterns of PAHs, which is useful for understanding the effects, sources, fates, and transport of PAHs in sediment in the study area, as well as for providing relevant information for environmental quality management and forensic studies.

Polycyclic aromatic hydrocarbons in coastal rivers in Jiangsu Province, China: Spatial distribution, source apportionment and human impacts

The ocean is the ultimate sink for all pollutants, rivers are important channels for land-based pollutants to enter the oceans. Riverine transport of polycyclic aromatic hydrocarbons (PAHs) to coastal seas in China poses environmental threats. This study examined the spatial and temporal distribution of PAHs in coastal rivers in Yancheng City in Jiangsu Province of China, with the aim of identifying their likely sources, concentrations, and influencing factors. Surface sediments were taken from the Xinyanggang River (XYR) and the Sheyang River (SYR). The concentrations of Ʃ16PAHs in river sediments were measured on average 477.05 ng/g dry weight (dw), with values varying from 2.18 to 6351.42 ng/g, indicating a moderate pollution level, with a dominance of high molecular weight (HMW) PAHs. The XYR exhibited significantly higher PAHs concentrations compared to the SYR. The key sources of PAHs were vehicle emissions (47.87%), coal and natural gas combustion (35.07%). Geographically weighted regression and redundancy analysis linked PAHs pollution to distinct land use patterns and socioeconomic indicators, highlighting urban land as the major contributor, driven by high urbanization and industrialization (70.91%). In XYR, industrial activities and transport emissions were major contributors, while in SYR, agricultural activities predominantly influenced PAHs pollution. Urgent mitigation strategies are needed to reduce PAHs pollution in river sediments, mitigating ecological and human risks associated with these contaminants.

Reduction strategies of polycyclic aromatic hydrocarbons in farmland soils: Microbial degradation, plant transport inhibition, and their mechanistic analysis

This study focuses on the abatement of polycyclic aromatic hydrocarbons (PAHs), a global pollutant, in farmland soils. Seven controlled PAHs in China were used as the target ligands, and four key target receptors degradable PAHs and two key target receptors transport PAHs were used as the target receptors. Firstly, the degradation abilities of the four key target receptors on PAHs were quantified, and the dominant target receptors that could efficiently degrade PAHs were screened out. Then, the co-degradation abilities of PAHs under the coexistence of the dominant target receptors (microbial diversity) were assessed, and 30 external condition-adding schemes to promote the microbial (co-)degradation of PAHs were designed. In addition, the microbial dominant target receptor mutants and the plant key target receptor mutants were obtained, the degradation and transportation of PAHs were improved by 8.06%∼22.27% and 39.86%∼45.43%. Finally, the mechanism analysis of PAHs biodegradation and transportation found that the Van der Waals interactions dominated the enhancement of PAHs’ degradation in soil, and the solvation capacity dominated the decrease of PAHs’ transportation in plant. This study aims to provide theoretical support for the prevention and control of PAHs residue pollution in farmland soil, as well as the protection of human dietary health.

Autumn and spring observations of PM2.5-bound polycyclic aromatic hydrocarbons and nitro-polycyclic aromatic hydrocarbons in China and Japan

The transboundary transport of polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs (NPAHs) aggravated by the East Asian winter monsoon is a major atmospheric environmental issue in East Asia. To thoroughly elucidate the role of the East Asian monsoon on regional PAH and NPAH pollution in East Asia, PM2.5-bound PAHs and NPAHs were investigated concurrently at five sites in Beijing and Shenyang in China and Tsukuba, Kanazawa, and Wajima in Japan in autumn (November 2018) and spring (March 2019). During both autumn and spring sampling periods, the concentrations of PM2.5, PAHs, and NPAHs at sites in China were 1–2 orders of magnitude higher than those at sites in Japan, and showed an opposite temporal variation, with higher concentrations during the autumn sampling period due to intensive emissions and unfavourable weather conditions. During the sampling periods, PAHs at the Beijing and Shenyang sites had mixed sources of traffic emissions and coal and biomass combustion, while those at the Tsukuba, Kanazawa, and Wajima sites were mainly characterized by domestic traffic emissions. In addition, NPAHs at the five sites were jointly affected by primary combustion sources and atmospheric generation, with a greater contribution of atmospheric generation to the Beijing and Shenyang sites. Based on backwards trajectory clustering and concentration-weighted trajectory analysis, external contributions to PM2.5, PAHs, and NPAHs at each site were relatively stable during the two sampling periods, and potential source areas were mainly distributed in domestic cities and nearby sea areas. Therefore, the apparent temporal differences in the characteristics and sources of pollutants between sites in the two countries indicate that transboundary pollution dominated by the East Asian winter monsoon was unobvious in autumn and spring. The results of the study provide a time-specific solution for the effective management of regional air pollution during the East Asian winter monsoon.

Expeditious profiling of polycyclic aromatic hydrocarbons transport and obstruction mechanisms in crop xylem sap proteins via proteomics and molecular docking

Polycyclic aromatic hydrocarbons (PAHs) pose significant environmental risks due to their toxicity and carcinogenic properties. This research seeks to pinpoint protein targets in crop xylem sap related to PAH contamination and delve into their protein-ligand interactions using computational tools. Proteomic assessment revealed differentially expressed proteins (DEPs), which were subjected to virtual high-throughput screening. Notably, the phenanthrene's influence on xylem sap proteins in maize and wheat was more pronounced than in soybean, with DEPs expression peak at 24 h post-treatment. Maize DEPs were predominantly associated with lipid biosynthesis. Phenanthrene impacted cell membrane hydrophobicity, limiting PAH adsorption and decreasing its concentration in maize xylem sap. Wheat DEPs exhibited an increase in ABC transporters after 24 h of phenanthrene exposure. ABC transporters interacted with stress-responsive proteins like C6TIY1-Co-chaperone p23 and others that either facilitate or inhibit PAH transport, including Indeno[1,2,3-cd]Pyrene and C6TIY1-Co-chaperone protein p23. Both maize and wheat created high-affinity complexes between specific proteins and PAHs, influencing their transport. This study provides insights into the mechanisms of PAH regulation and movement within plant xylem.

A trade-off in activated biochar capping of complex sediment contamination: reduced PAH transport at the cost of potential As mobilisation

PurposeThe effect of thin-layer capping with activated biochar on sediment-to-water flux was investigated. For the first time, the diffusion of both polycyclic aromatic hydrocarbons (PAHs) and arsenic (As) were studied simultaneously. The fate of As was investigated, under successive dysoxic and oxic conditions, in order to assess and discuss potential trade-off effects when using biochar as an active sorbent for capping of multi-contaminated sediments.MethodsSediments from the Bureå bay (Sweden), contaminated with PAH and metal elements including As and Hg, were capped with activated biochar and/or bentonite in simple microcosm test systems in the laboratory. The contaminant transport from sediment through the capping to water body was studied by sampling metals in the water phase above the cap over time, or PAH in a heptane layer over water, at regular time intervals.ResultsConsistently with the limited previous studies, reductions were observed (e.g., 60–65% for 15-PAH, 100% for chrysene) in sediment-to-water PAH fluxes upon biochar-based thin-layer capping. However, the most important novel finding revealed ambiguous effects of biochar capping on redox-sensitive elements, in particular As. Under the microcosm conditions of the experiment, where pH was affected by the capping material, biochar treatments favoured As mobility under oxic conditions, directly and/or via effects on Fe speciation. While capping limited the diffusion of As under dysoxic conditions, this also favoured greater As mobility under oxic water conditions compared to no capping.ConclusionDesign and monitoring of capping of PAH contaminated sediments should account for potential negative effects on co-occurring contaminants.

Atmospheric Transport of Polycyclic Aromatic Hydrocarbons into Three Alpine Valleys: Influence of Local-Scale Wind Patterns and Chemical Partitioning.

Current understanding of atmospheric transport of polycyclic aromatic hydrocarbons (PAHs) is limited in alpine areas due to complex meteorology and topography. To better understand atmospheric transport in these areas, we measured 16 PAHs in lichens, biomonitors of atmospheric PAHs, along three transects extending from a highway into otherwise remote alpine valleys. While the valleys neighbored one another and were morphologically similar, they differed in their orientation relative to regional winds. In the valley characterized by regional winds oriented up-valley, PAH concentrations in lichens remained consistent across the transect. In the other two valleys, where regional winds were oriented down or across the valley, 3-6 ring PAHs declined rapidly with increasing distance from the highway, and PAH concentrations in the lichens declined more rapidly for higher molecular weight PAHs than lower molecular weight PAHs. We hypothesize that this trend was driven by differences in gas-particle partitioning and vegetative scavenging between PAH congeners. These results illustrate the importance of both physical transport and chemical partitioning in alpine areas where small differences in topography can lead to significant differences in chemical transport.

Preferential association of polycyclic aromatic hydrocarbons (PAHs) with soil colloids at an e-waste recycling site: Implications for risk of PAH migration to subsurface environment

Polycyclic aromatic hydrocarbon (PAH) contamination at e-waste recycling sites poses high ecological and human-health risks. Of note, PAHs in surface soils can be mobilized through colloid-facilitated transport, and may migrate into the subsurface and pollute groundwater. Here, we show that the colloids released from the soil samples at an e-waste recycling site in Tianjin, China contain high concentrations of PAHs, with total concentrations of 16 PAHs as high as 1520 ng/g dw. Preferential association of the PAHs with the colloids is observed, with the distribution coefficients of PAHs between colloids and bulk soil often above 10. Source diagnostic ratios show that soot-like particles are the main source of PAHs at the site, due to the incomplete combustion of fossil fuels, biomass, and electronic wastes during the e-waste dismantling practices. Due to their small sizes, a large fraction of these soot-like particles can be remobilized as colloids, and this explains the preferential association of PAHs with colloids. Moreover, the colloids-soil distribution coefficients are higher for the low-molecular-weight PAHs than for the high-molecular-weight ones, possibly attributable to the different binding routes/modes of these two groups of PAHs to the particles during combustion. Notably, the preferential association of PAHs with colloids is even more pronounced for the subsurface soils, corroborating that the presence of PAHs in the deeper soils is primarily the results of downward migration of PAH-bearing colloids. The findings highlight the important role of colloids as a vector for the subsurface transport of PAHs at e-waste recycling sites, and call for further understanding of colloid-facilitated transport of PAHs at e-waste recycling sites.

Exploring sorption of pesticides and PAHs in microplastics derived from plastic mulch films used in modern agriculture

The sorption and vector effect of microplastics on the transfer of pesticides and polycyclic aromatic hydrocarbons (PAHs), as well as its impact on agriculture remain largely unexplored. This comparative study is first to investigate the sorption behavior of different pesticides and PAHs at environmentally realistic concentrations by model microplastics and microplastics derived from polyethylene mulch films. Sorption was found to be up to 90% higher in the case of microplastics derived from mulch films as opposed to pure polyethylene microspheres. For microplastics from mulch films, the sorption percentages for pesticides in media containing CaCl2 were reported to be: pyridate (75.68% and 52.44%), fenazaquin (48.54% and 32.02%), pyridaben (45.04% and 56.70%), bifenthrin (74.27% and 25.88%), etofenprox (82.16% and 54.16%) and pyridalyl (97.00% and 29.74%) at 5 μg/L and 200 μg/L pesticide concentration levels respectively. For PAHs, the sorption amounts were: naphthalene (22.03% and 48.00%), fluorene (38.99% and 39.00%), anthracene (64.62% and 68.02%) and pyrene (75.65% and 86.38%) at 5 μg/L and 200 μg/L PAH concentration levels respectively. Sorption was influenced by the octanol-water partition coefficient (log Kow) and ionic strength. Kinetics of the process in the case of sorption of pesticides were best explained by pseudo-first order kinetic model (R2 between 0.90 and 0.98) while the best fitting isotherm model was Dubinin-Radushkevich (R2 between 0.92 and 0.99). Results suggest the presence of surface level physi-sorption through a micropore volume filling mechanism and the role of hydrophobic and electrostatic forces. Pesticide desorption data in polyethylene mulch films indicate that pesticides with high log Kow were almost completely retained in mulch films, while those with lower log Kow were desorbed rapidly into the surrounding media. Our study highlights the role of microplastics from plastic mulch films as vectors for pesticide and PAH transport at environmentally realistic concentrations and the factors that influence it.