Perfluoroalkyl Substances Research Articles

Dynamic Storage, Release, and Enrichment of some Per‐ and Polyfluoroalkyl Substances in the Groundwater Table Fluctuation Zone: Transport Processes Requiring Further Consideration

Dynamic Storage, Release, and Enrichment of some Per‐ and Polyfluoroalkyl Substances in the Groundwater Table Fluctuation Zone: Transport Processes Requiring Further Consideration

Role of Fluorocarbon Chain Length in the Adsorption of Perfluoroalkyl Substances on Nanoplastic Particles

Role of Fluorocarbon Chain Length in the Adsorption of Perfluoroalkyl Substances on Nanoplastic Particles

Per- and poly-fluoroalkyl substances in aquatic ecosystems and wastewater treatment works in Africa: Occurrence, ecological implications, and future perspectives

The increasing levels of industrialization and urbanization have led to the generation of significant amounts of wastewater and waste products, often containing chemicals like per- and poly-fluoroalkyl substances (PFASs) commonly found in consumer products. PFASs are known for their persistence, ubiquity, and ecotoxicological impacts, raising concerns about potential harm to ecosystems. This paper reports the occurrence and evaluates the ecological risks of PFASs in aquatic ecosystems and wastewater treatment works (WWTWs) across Africa. We reviewed 32 papers published in the period 2009–2024 and identified a total of 35 PFAS compounds in surface waters, wastewater, sediments, fish, crocodiles, and invertebrates. Much of the reported studies came from South Africa, followed by Kenya and Nigeria. PFAS concentrations in Africa were <0.7–390.0 ng L−1 in surface waters, 0.05–772 ng g−1 dw in sediments, and <0.2–832 ng L−1 in wastewater, while the highest levels in fish and invertebrates were 460.7 and 35.5 ng g−1 ww, respectively. The PFAS levels were in the same range of data as those reported globally. However, the high concentrations of PFASs in sediments and wastewater suggest areas of point contamination and a growing risk to aquatic ecosystems from effluent discharges. Calculated risk quotients suggested that, in Africa, organisms in river systems face greater risks due to exposure to PFASs compared to those in lakes, while marine organisms might face higher risks compared to freshwater organisms. Future studies should focus on PFAS contamination sources, especially WWTWs, as emerging sources of PFASs in aquatic systems.

Making waves: The progress of management strategies for cleaning and rinsing of PFAS-impacted fire suppression systems

Aircraft rescue firefighting (ARFF) vehicles often contain residual levels of per- and polyfluoroalkyl substances (PFAS) due to the global use of legacy and current use of aqueous film-forming foam (AFFF) for class B firefighting. However, numerous countries are transitioning to fluorine-free foam (F3) alternatives. There is, thus, an urgent need to develop efficient methods to rinse and clean interior ARFF surfaces thereby avoiding expensive replacement costs and preventing further discharge of PFAS to the environment. However, the unique self-assembly behavior of amphiphilic PFAS is a complicating factor that can result in measurable levels of PFAS within replacement F3 following cleanout efforts (i.e., the rebound effect). This Making Waves article aims to elucidate the emerging challenges associated with cleanout of impacted ARFF vehicles and introduce the current efforts for PFAS management of rinsate derived from cleanout of impacted fire suppression infrastructure.

Impact of polyfluoroalkyl chemicals and volatile organic compounds exposure on lung function of American adults

BackgroundEnvironmental chemicals, such as Perfluoroalkyl and polyfluoroalkyl substances (PFAS) and volatile organic compounds (VOCs), and the association between the combined exposure of these chemicals and human lung function remains unclear. This study aimed to explore the effects of mixed exposure to PFAS and VOCs on lung function in the general population of the United States and investigate their potential mechanisms. MethodsData from 30442 respondents were selected for analysis during the US National Health and Nutrition Examination Survey (NHANES) database from 2007 to 2012. Linear models, weighted quantile (WQS) regression, quantile g calculation (QGC), and Bayesian kernel machine regression (BKMR) were used to evaluate the contribution of individual components. Moreover, the interactions between substances in the dose-response relationship mixture of multiple environmental chemical exposures and lung function were also evaluated. The Benjamini-Hochberg method was used to correct multiple tests. FindingsUnivariate analysis showed that nitromethane was negatively correlated with FEV1 (β =−0.052), FVC (β =−0.056), and PEF (β =−0.065), while perfluorohexanesulfonic acid was positively associated with FEV1 (β = 0.026), FVC (β = 0.024), FEF25-75% (β = 0.012), and PEF (β = 0.029). Multivariate analysis showed that chloroform and perfluorohexane sulfonic acid were positively associated with lung function (P <0.05), and perfluorohexane sulfonic acid contributed the most. Nitromethane and perfluorodecanoic acid were negatively associated with lung function (P < 0.05), and perfluorodecanoic acid contributed the highest weight in the negative direction. When all chemicals were in the 50th percentile, the environmental chemical mixture had no significant consistent effect or dose-response on lung function. There were interactions among various environmental chemicals within the mixture except for 2-N-methyl-PFOSA acetate and bromodichloromethane. InterpretationThese results suggest that environmental mixture exposure is associated with abnormal lung function in American adults, and the interaction of various substances in the mixture affects its physiological and chemical effects.

Shift from legacy to emerging per- and polyfluoroalkyl substances for watershed management along the coast of China

Per- and polyfluoroalkyl substances and their short-chain alternatives have attracted world-wide attention due to their widespread presence and persistence in the environment. However, the sources, environmental fate, and driving forces of PFAS in coastal ecosystems remain poorly understood. In this study, the spatial distribution, source apportionment, and driving mechanisms of PFAS were investigated through a comprehensive analysis of water samples collected along the China's coastline. The concentrations of Σ25PFAS in water samples followed a general pattern, with higher levels observed in northern coastal zones of China than the south, ranging from 0.72 to 1872.21 ng L−1. PFOA and PFBA were dominant. Emerging short-chain PFAS, such as PFBS, PFBA, F-53B and GenX, were frequently detected, with detection rates of 97%, 99%, 95% and 77%, respectively. This indicated a shift in coastal PFAS contamination from legacy compounds to emerging short-chain alternatives. Source apportionment using the Positive Matrix Factorization model identified key contributors to PFAS pollution, including textile production, volatile precursors, precious metal industries, aqueous film-forming foam, metal-plating, electrochemical fluorination, and fluoropolymer manufacturing. Additionally, PFAS concentrations were significantly positively correlated with cultivated land, urban area, and wastewater discharge, while negatively correlated with annual precipitation and woodland coverage (p < 0.05). Socio-economic development was identified as a major driver of PFAS emissions, while the hydrological factors and vegetation coverage can significantly enhance watershed resilience against PFAS pollution.

A critical review of wastewater-based epidemiology as a tool to evaluate the unintentional human exposure to potentially harmful chemicals.

Wastewater-based epidemiology (WBE) is a powerful tool to gather epidemiological insights at the community level, providing objective data on population exposure to harmful substances. A considerable portion of the human exposure to these potentially harmful chemicals occurs unintentionally, unlike substances such as pharmaceuticals, illicit drugs, or alcohol. In this context, this comprehensive review analyzes WBE studies focused on classes of organic chemicals to which humans are unintentionally exposed, namely organophosphorus flame retardants, per- and polyfluoroalkyl substances (PFAS), benzotriazoles and benzothiazoles, phthalates and terephthalates, benzophenones, pesticides, bisphenols, and parabens. The review highlights some advantages of WBE for public health surveillance, e.g., non-invasive analysis, predictive capability, nearly real-time data, population-wide insights, no ethical approval, and unbiased sampling. It also discusses challenges and future research directions in WBE regarding exposure to harmful chemicals from various sources. The review emphasizes the critical role of wastewater sampling, sample preparation, quality control, and instrumental analysis in achieving accurate and reliable results. Furthermore, it examines the selection of human biomarkers for WBE studies and explores strategies to link WBE with human biomonitoring (HBM), which together enhance both the precision and effectiveness of exposure assessments.

The potential mediating role of the gut microbiome and metabolites in the association between PFAS and kidney function in young adults: A proof-of-concept study

BackgroundChronic kidney disease (CKD) affects over 10 % of the global population and can lead to kidney failure and death. Exposure to per- and polyfluoroalkyl substances (PFAS) is associated with increased risk of CKD, yet studies examining the mechanisms linking PFAS and kidney function are lacking. In this exploratory study, we examined longitudinal associations of PFAS exposure with kidney function, and tested if associations were mediated by altered gut bacterial taxa or plasma metabolites using a multi-omics mediation analysis. MethodsSeventy-eight young adults from the Children's Health Study were included in this longitudinal cohort study. At baseline, seven plasma PFAS and untargeted plasma metabolomics were measured using liquid chromatography/mass-spectrometry. Baseline gut bacterial abundance was characterized using 16S rRNA sequencing and examined at the genus level. At follow-up, serum creatinine and cystatin-C concentrations were quantified to estimate glomerular filtration rate (eGFR). High-dimensional multi-omics analyses were conducted to assess the association between baseline PFAS exposure with follow-up eGFR, mediated by gut microbiome and circulating metabolite levels. ResultsPFAS burden score, a variable developed to estimate exposure to chemical mixtures, was associated with kidney function. Each standard deviation increase in baseline PFAS burden score was associated with a 2.4 % lower eGFR at follow-up (95 % CI:[0.1 %,4.8 %]). Following high-dimensional mediation analyses with the microbiome and circulating metabolites, a joint component (characterized by reduced Lachnospiraceae and 17b-estradiol and increased succinate, retinoate and dodecanoic acid) and a metabolite component (characterized by increased hypotaurine and decreased D-pinitol and ureidopropionate) mediated 38 % and 50 % of the effect between PFAS burden score and eGFR, respectively. ConclusionOur proof-of-concept analysis provides the first evidence that reduced short-chain fatty acid-producing bacteria and anti-inflammatory metabolites may link PFAS exposure with impaired kidney function. This study raises the possibility of future targeted interventions that can alter gut microbiome or circulating metabolite profiles to prevent PFAS induced kidney damage.

Removal of perfluoroalkyl acids and precursors with silylated clay: Efficient adsorption and enhanced reuse

Organically modified clays (organoclays) have been considered effective adsorbents for the treatment of per- and polyfluoroalkyl substances (PFAS). However, the stability of organoclays prepared through the conventional cation exchange approach has been a major concern for their practical application. In this study, we reported the development of a new organically functionalized clay by grafting pillared clay substrate with an organosilane through covalent bonding. The performance of the silylated clay (QAG-ZrMT) was systematically compared with an organoclay prepared from ion exchange (HDTMA-ZrMT) for the adsorption of two legacy perfluoroalkyl acids: perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS), and two precursor compounds 5:3 fluorotelomer carboxylic acid (5:3FTCA) and 6:2 fluorotelomer sulfonic acid (6:2FTS). Compared to HDTMA-ZrMT, QAG-ZrMT showed substantially improved performance for adsorption of less hydrophobic PFAS (e.g., 5:3FTCA), which could be related to the stronger electrostatic interactions between PFAS and QAG-ZrMT than HDTMA-ZrMT. More importantly, QAG-ZrMT could be conveniently regenerated and reused for multiple cycles with robust performance. In contrast, HDTMA-ZrMT almost completely lost its capacity for PFAS removal after regeneration, due to the loss of organic functional groups during solvent regeneration. Results can shed light on the design of efficient and regenerable organoclay adsorbents for remediation of PFAS-contaminated water matrices.

Simulating PFAS transport in effluent-irrigated farmland using PRZM5, LEACHM, and HYDRUS-1D models.

Application of wastewater effluent to agricultural lands can serve as a sustainable approach to meet irrigation and nutrient needs for crop production. While nitrogen and phosphorous loadings can be effectively managed, concerns have been raised regarding the fate of emerging contaminants, including per- and polyfluoroalkyl substances (PFAS), which are widely detected in wastewater effluent. The objective of this paper was to evaluate the ability of three unsaturated flow and transport models, Pesticide Root Zone Model 5 (PRZM5), LEACHM, and HYDRUS-1D, to predict the distribution of PFAS in the soil profile at the Pennsylvania State University Living Filter site, which has received daily wastewater effluent applications for several decades. The models were modified to include adsorption at the air-water interface (AWI), which has been shown to be an important factor governing PFAS transport and phase distribution in the vadose zone. Simulations showed that PRZM5 did not accurately reproduce the observed perfluorooctanesulfonic acid (PFOS) behavior, which was attributed to the "tipping bucket" approach used for water flow that results in the disappearance of AWI during water flow. In contrast, both LEACHM and HYDRUS-1D captured the observed retention of PFOS and perfluorooctanoic acid (PFOA) over a 50-year simulation period. Due to differences in the approach used to calculate the AWI area, LEACHM predicted greater accumulation of PFOS and PFOA at the AWI compared to HYDRUS-1D. These findings indicate that mathematical models that directly account for unsaturated water flow and adsorption at the AWI are able to provide reasonable predictions of long-term PFAS leaching resulting from land application of wastewater effluent.

Embryonic 6:2 Fluorotelomer Alcohol Exposure Disrupts the Blood‒Brain Barrier by Causing Endothelial‒to‒Mesenchymal Transition in the Male Mice.

6:2 Fluorotelomer alcohol (6:2 FTOH) is a raw material used in the manufacture of short-chain poly- and perfluoroalkyl substances. Our previous study revealed that gestational exposure to 6:2 FTOH can impair blood‒brain barrier (BBB) function in offspring, accompanied by anxiety-like behavior and learning memory deficits. The aim of this study was to further investigate the specific mechanism by which maternal exposure to 6:2 FTOH resulted in impaired BBB function in offspring mice. Pregnant mice were orally administered different doses of 6:2 FTOH (0, 5, 25, and 125mg/kg/day) from gestation day 8.5 until delivery. These results confirmed that maternal 6:2 FTOH exposure impaired BBB function and disrupted the brain immune microenvironment. Subsequent investigations revealed that endothelial-to-mesenchymal transition (EndMT) in the cerebral microvascular endothelium of offspring may be the mechanism mediating functional disruption of the BBB. Mechanistic studies revealed that exposure to 6:2 FTOH upregulated ETS proto-oncogene 1 (ETS1) expression via the tumor necrosis factor-α/extracellular signal-regulated kinase 1/2 signaling pathway, which mediated disturbances in energy metabolism, leading to impaired actin dynamics and subsequently triggering the EndMT phenotype. This is the first finding indicating that gestational 6:2 FTOH exposure caused functional impairment of the BBB through ETS1-mediated EndMT in cerebral microvascular endothelial cells, potentially providing novel insight into the environmental origins of neurodevelopmental disorders.

Tissue distribution, biomagnification, human health risk, and risk mitigation of perfluoroalkyl acids (PFAAs) in the aquatic food web of an urban fringe lake: Insights from urban-rural and seasonal scales

Perfluoroalkyl acids (PFAAs), renowned for their exceptional physical and chemical properties, are ubiquitous in urban and rural environments. Despite their widespread usage, more knowledge is needed concerning their accumulation and transfer mechanisms within the aquatic food webs of urban fringe lakes, especially across rural-urban and seasonal scales. This study investigated the tissue distribution, bioaccumulation, biomagnification, associated human health risks, and potential risk mitigation strategies of 15 PFAAs within the food web of Luoma Lake, a prototypical urban fringe lake. All targeted PFAAs were detected in samples, with ∑PFAA concentrations ranging from 116.97 to 564.26 ng/g dw in muscles and 26.96–1850.95 ng/g dw in viscera. Spatial variations revealed significantly higher ∑PFAA concentrations in the muscles from the urban subregion (∑PFAA: 359.66 ± 76.48 ng/g dw) compared to the rural subregion (∑PFAA: 328.86 ± 87.51 ng/g dw). Seasonal fluctuations impacted PFAA concentrations in fish and crustacean muscles but exhibited negligible effects on bivalve muscles. Spatial variations only influenced PFAA concentrations in specific viscera (gill, liver, kidney), while seasonal changes had minimal effects on viscera. The organisms demonstrated varying bioaccumulation capacities, with crustaceans displaying the highest bioaccumulation potential, followed by crustaceans and fish. Both spatial and seasonal variations modulated the bioaccumulation patterns of PFAA in muscles, whereas bioaccumulation in viscera was only influenced by seasonal factors. Notably, PFAA biomagnification along the food web was exclusively governed by spatial distribution, remaining unaffected by seasonal changes. The human health risk assessment underscored the potential adverse health impacts of PFOS and PFOA, particularly on young children (aged 2 to <6 years). This study further proposed comprehensive recommendations for mitigating PFAA-induced health risks, encompassing source control, selective consumption, pre-cooking treatments, and strategic cooking method selection. This research provides crucial insights into the ecological behaviors and health implications of PFAA in urban fringe lakes.

Using syringe filtration after lab-scale adsorption processes potentially overestimates PFAS adsorption removal efficiency from non-conventional irrigation water.

The adsorption process, known for its cost-effectiveness and high efficiency, has been extensively investigated at the laboratory scale for removing per- and polyfluoroalkyl substances (PFAS) from non-conventional irrigation water. However, a syringe filtration step is commonly used when quantifying PFAS removal during this adsorption process, potentially leading to PFAS retention onto the filters and an overestimate of adsorption removal efficiency. Here, we assessed the retention of three prevalent PFAS (i.e., perfluorooctanoic acid [PFOA], perfluorooctane sulfonic acid [PFOS], and perfluorobutanoic acid [PFBA]) on six syringe filters. When filtering distilled deionized water spiked with 1µg/L and 100µg/L of each PFAS, we observed the highest and lowest PFAS recovery percentages by mixed cellulose ester (MCE) (0.20µm, 25mm; 97±11%, 101±4.8%) and polytetrafluoroethylene (0.45µm, 13mm; 61±37%, 80±28%), respectively. Under the initial concentration of 1µg/L and 100µg/L, PFOS had recovery percentages of 55±25% and 68±24%, significantly lower than 96±12% and 99±5% for PFOA and 95±8% and 97±4% for PFBA, highlighting the importance of PFAS functional groups. PFAS recovery percentage increased with filtration volume in the order of 80±28% (1mL)<85±21% (5mL)<90±18% (10mL). Using MCE to filter treated municipal wastewater spiked with 1µg/L and 100µg/L of each PFAS, we found recovery percentages>90% for all three PFAS. Our study underscores the significance of syringe filter selection and potential overestimate of PFAS removal efficacy by the lab-scale adsorption processes.

Characterizing the Areal Extent of PFAS Contamination in Fish Species Downgradient of AFFF Source Zones.

Most monitoring programs next to large per- and polyfluoroalkyl substances (PFAS) sources focus on drinking water contamination near source zones. However, less is understood about how these sources affect downgradient hydrological systems and food webs. Here, we report paired PFAS measurements in water, sediment, and aquatic biota along a hydrological gradient away from source zones contaminated by the use of legacy aqueous film-forming foam (AFFF) manufactured using electrochemical fluorination. Clustering analysis indicates that the PFAS composition characteristic of AFFF is detectable in water and fishes >8 km from the source. Concentrations of 38 targeted PFAS and extractable organofluorine (EOF) decreased in fishes downgradient of the AFFF-contaminated source zones. However, PFAS concentrations remained above consumption limits at all locations within the affected watershed. Perfluoroalkyl sulfonamide precursors accounted for approximately half of targeted PFAS in fish tissues, which explain >90% of EOF across all sampling locations. Suspect screening analyses revealed the presence of a polyfluoroketone pharmaceutical in fish species, and a fluorinated agrochemical in water that likely does not accumulate in biological tissues, suggesting the presence of diffuse sources such as septic system and agrochemical inputs throughout the watershed in addition to AFFF contamination. Based on these results, monitoring programs that consider all hydrologically connected regions within watersheds affected by large PFAS sources would help ensure public health protection.

Quantitative assessment of poly- and perfluoroalkyl substances (PFASs) in aqueous film forming foam (AFFF)-impacted soils: a comparison of analytical protocols.

Quantitatively assessing all per- and poly fluoroalkyl substances (PFASs) in an environmental sample, particularly soils impacted by aqueous film forming foams (AFFFs), has proven to be a challenge. To make such an assessment, a comprehensive sample processing procedure and analytical tool must be used. However, doubts remain whether current analytical tools such as high-resolution mass spectrometry (HRMS) with targeted quantitation and semi-quantitative analysis of suspects (Semi-Q HRMS) or total organic fluorine (TOF) are capable of accurately quantifying all non-polymeric PFASs in a sample. Further, current comprehensive soil PFAS HRMS methods are incompatible with TOF, preventing direct comparisons of the approaches. To enable direct comparisons, a soil sample processing procedure that is comprehensive as well as compatible with multiple analytical tools is needed. In this study, we assessed the performance of a previously developed soil PFAS method, EPA Method 1633, and a hybrid solid phase extraction (SPE)-based method for characterizing AFFF-impacted soil composites while maintaining compatibility with multiple analytical tools (i.e., Semi-Q HRMS and TOF). Comparative results for AFFF-impacted soil composites indicate analysis via EPA Method 1633 (as compared to the novel hybrid method) results in maybeup to 75% of the PFAS mass being missed by only analyzing for compounds listed in EPA Method 1633. Simply expanding the EPA Method 1633 analyte list was insufficient to account for the missing mass: up to 69% of the PFAS mass was still missed because of EPA Method 1633's extraction and cleanup bias. Additionally, the novel method developed offers a more comprehensive analysis with minimal reductions to sensitivity when compared to those reported in EPA Method 1633, with limits of quantification ranging from 0.12 to 2.4 ng/g as compared to 0.16-4.0 ng/g, respectively. For these reasons, an alternative hybrid SPE-based method is proposed for comprehensive evaluation of PFASs in AFFF-impacted soils.

Simultaneous and High-Throughput Analytical Strategy of 30 Fluorinated Emerging Pollutants Using UHPLC-MS/MS in the Shrimp Aquaculture System.

This study established novel and high-throughput strategies for the simultaneous analysis of 30 fluorinated emerging pollutants in different matrices from the shrimp aquaculture system in eastern China using UHPLC-MS/MS. The parameters of SPE for analysis of water samples and of QuEChERS methods for sediment and shrimp samples were optimized to allow the simultaneous detection and quantitation of 17 per- and polyfluoroalkyl substances (PFASs) and 13 fluoroquinolones (FQs). Under the optimal conditions, the limits of detection of 30 pollutants for water, sediment, and shrimp samples were 0.01-0.30 ng/L, 0.01-0.22 μg/kg, and 0.01-0.23 μg/kg, respectively, while the limits of quantification were 0.04-1.00 ng/L, 0.03-0.73 μg/kg, and 0.03-0.76 μg/kg, with satisfactory recoveries and intra-day precision. The developed methods were successfully applied to the analysis of multiple samples collected from aquaculture ponds in eastern China. PFASs were detected in all samples with concentration ranges of 0.18-0.77 μg/L in water, 0.13-1.41 μg/kg (dry weight) in sediment, and 0.09-0.96 μg/kg (wet weight) in shrimp, respectively. Only two FQs, ciprofloxacin and enrofloxacin, were found in the sediment and shrimp. In general, this study provides valuable insights into the prevalence of fluorinated emerging contaminants, assisting in the monitoring and control of emerging contaminants in aquatic foods.

The soil-air interfacial migration process of volatile PFAS at the contaminated sites: Evidence from stable carbon isotopes with CSIA

Volatile per- and polyfluoroalkyl substances (PFAS) are prone to transport among various environmental media, with the soil-air interfacial migration process being an important pathway that significantly influences their environmental fate. To assess the migration and transformations of target volatile PFAS at contaminated site using compound-specific stable isotope analysis (CSIA), it is necessary to understand the isotopic fractionation that occurs during their transfer from soil to air. We have established methods for pre-treatment and GC/CSIA analysis methods of target volatile PFAS in soil and air samples and ensured the accuracy of carbon isotope analysis. GC/IRMS δ13C measurements showed optimal precision at instrumental response above 1.35–2.75 Vs, with recommended minimum on-column C levels of 1.67–5.00 nmol for target volatile PFAS. Stable carbon isotope fractionation factors related to the soil-air interfacial migration process for target volatile PFAS were determined by performing laboratory simulations. The observed εsoil-air values are all negative, suggesting that the soil-air interfacial migration process for target volatile PFAS is kinetic fractionation, the removal of molecules containing lighter isotopes. By comparing the simulated and experimentally observed δ13C (‰) values of target volatile PFAS, we found consistent trends in the soil and inverse trends in the air. These δ13C (‰) values and the related isotope fractionation model provide valuable insights into the isotopic behavior of target volatile PFAS during soil-air interfacial migration process, aiding in the assessment of their environmental fate.

Microplastic and associated emerging contaminants in marine fish from the South China Sea: Exposure and human risks

Microplastics can act as vectors of chemical contaminants in aquatic environments, but the extent to which this phenomenon contributes to chemical exposure in marine organisms remains poorly understood. We investigated the occurrence of microplastics and emerging contaminants (ECs), including antibiotics and per- and polyfluoroalkyl substances (PFAS) in 14 marine fish species. Microplastics were detected in all marine fish species, mainly in the gastrointestinal tract. Fluoroquinolones and tetracyclines were the dominant antibiotics in fish muscles with maximum concentrations of 24.84 and 26.95 ng g−1 ww, while perfluorooctanesulfonic acid (PFOS, 0.039–0.95 ng g−1 ww) was the dominant component in the PFAS profile. Fish with more microplastics had significantly higher concentrations of fluoroquinolones and perfluoroalkyl acids than fish with less microplastics (p < 0.05), but the correlation was not observed in other chemicals. Structural equation modeling revealed the contribution of microplastics in fish on the level of ECs contamination. The health quotient value indicated the low health risk of single compounds via fish consumption to humans; however, the combined risk of microplastics and ECs still needs to be considered. This work highlights the link between microplastics with associated ECs ingested by aquatic organisms and the human health risk of consuming polluted seafood.

Quantification of Extractable Total Per- and Polyfluoroalkyl Substances in Water Using Persulfate Preoxidation, Solid Phase Extraction, and Chemical Defluorination with Sodium Biphenyl or Ion-Pair Formation with Methylene Blue

Quantification of Extractable Total Per- and Polyfluoroalkyl Substances in Water Using Persulfate Preoxidation, Solid Phase Extraction, and Chemical Defluorination with Sodium Biphenyl or Ion-Pair Formation with Methylene Blue

Combined toxicity of perfluoroalkyl substances and microplastics on the sentinel species Daphnia magna: Implications for freshwater ecosystems

Persistent chemicals from industrial processes, particularly perfluoroalkyl substances (PFAS), have become pervasive in the environment due to their persistence, long half-lives, and bioaccumulative properties. Used globally for their thermal resistance and repellence to water and oil, PFAS have led to widespread environmental contamination. These compounds pose significant health risks with exposure through food, water, and dermal contact. Aquatic wildlife is particularly vulnerable as water bodies act as major transport and transformation mediums for PFAS. Their co-occurrence with microplastics may intensify the impact on aquatic species by influencing PFAS sorption and transport. Despite progress in understanding the occurrence and fate of PFAS and microplastics in aquatic ecosystems, the toxicity of PFAS mixtures and their co-occurrence with other high-concern compounds remains poorly understood, especially over organisms’ life cycles.Our study investigates the chronic toxicity of PFAS and microplastics on the sentinel species Daphnia, a species central to aquatic foodwebs and an ecotoxicology model. We examined the effects of perfluorooctane sulfonate (PFOS), perfluorooctanoic acid (PFOA), and polyethylene terephthalate microplastics (PET) both individually and in mixtures on Daphnia ecological endpoints. Unlike conventional studies, we used two Daphnia genotypes with distinct histories of chemical exposure. This approach revealed that PFAS and microplastics cause developmental failures, delayed sexual maturity and reduced somatic growth, with historical exposure to environmental pollution reducing tolerance to these persistent chemicals due to cumulative fitness costs. We also observed that the combined effect of the persistent chemicals analysed was 59% additive and 41% synergistic, whereas no antagonistic interactions were observed. The genotype-specific responses observed highlight the complex interplay between genetic background and pollutant exposure, emphasizing the importance of incorporating multiple genotypes in environmental risk assessments to more accurately predict the ecological impact of chemical pollutants.