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Occurrence and Distribution of Per- and Polyfluoroalkyl Substances from Multi-Industry Sources to Water, Sediments and Plants along Nairobi River Basin, Kenya.

ABSTRACT: Per- and polyfluoroalkyl substances (PFAS) are ever-present pollutants in the environment. They are persistent and bio-accumulative with deleterious health effects on biota. This study assesses the levels of PFAS in environmental matrices along the Nairobi River, Kenya. An aggregate of 30 PFAS were determined in water, while 28 PFAS were detected in sediments and plants using solid phase extraction then liquid chromatography-mass spectrometric techniques. In water, higher levels of perfluoroundecanoic acids of up to 39.2 ng L^-1 were observed. Sediment and plant samples obtained in the midstream and downstream contained higher levels of perfluorooctanoic acid of up to 39.62 and 29.33 ng g^-1, respectively. Comparably, levels of long-chain PFAS were higher in water and sediments than in plants. Sediment/water log distribution of selected PFAS ranged between 2.5 (perfluoroundecanoic acid) and 4.9 (perfluorooctane sulfonate). The level of perfluorooctane sulfonate (1.83 ng L^-1) in water is above the acceptable level in surface water posing high human health and ecological risks. The observed PFAS concentrations and distribution were attributed mainly to multi-industries located along the river, among other sources. The knowledge of PFAS occurrence and distribution in Nairobi River, Kenya, provides important information to local regulatory agencies for PFAS pollution control.

SUBMITTER: Chirikona F

PROVIDER: S-EPMC9331875 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:Per- and polyfluoroalkyl substances (PFASs) have attracted scientific and regulatory attention due to their persistence, bioaccumulative potential, toxicity, and global distribution. We determined the accumulation and trophic transfer of 14 PFASs (5 short-chain and 9 long-chain) within the food web of the Yadkin-Pee Dee River of North Carolina and South Carolina, US. Food web components and pathways were determined by stable isotope analyses of producers, consumers, and organic matter. Analyses of water, sediment, organic matter, and aquatic biota revealed that PFASs were prevalent in all food web compartments. Biofilm, an aggregation of bacteria, fungi, algae, and protozoans and a basal resource for the aquatic food web, showed high PFAS accumulation (in 10 of 14 compounds), particularly for perfluorooctanoic acid, with the greatest mean concentration of 463.73 ng/g. The food web compartment with the most detections and greatest concentrations of PFASs was aquatic insects; all 14 PFASs were detected in individual aquatic insect samples (range of <limit of detection [<LOD] to 1670.10 ng/g of wet weight [WW]). These findings may suggest a trophic link between biofilm PFASs and aquatic insect PFASs. Individual fish tissue samples ranged from <LOD to 797.00 ng/g of WW, where perfluorooctanesulfonate (PFOS) was the dominant PFAS among all samples (64%). The ova of an imperiled fish, the robust redhorse (Moxostoma robustum), had concentrations of 10 PFASs (range of <LOD to 482.88 ng/g of WW) and the highest PFOS concentration (482.88 ng/g of WW), indicating a likely maternal transfer. The trophic magnification factors (TMFs) calculated in this study showed that various taxa accumulated PFAS compounds differently. PFBS, a short-chain PFAS compound that would presumably exhibit lesser TMFs, had nine values among our compartments and organisms >1.0 (range of 0.57 to 2.33); it is possible that an unmeasured PFBS precursor may be accumulating in biota and metabolizing to PFBS, leading to a higher than expected TMFs for this compound. Our findings demonstrate the prevalence of PFASs in a freshwater food web with potential implications for ecological and human health.

Project description:The presence of per- and polyfluoroalkyl substances (PFASs) in the food chain poses a threat to human health. Water and the atmosphere are the major transport pathways for PFASs in the environment, while water, soil and sediment are sinks. Herein, the concentrations and distributions of traditional and emerging PFASs in multi-environmental media samples in the Qiantang River watershed were comprehensively investigated. Twenty-five PFASs, including seven emerging PFASs, were identified. The concentrations in water, soil, sediment and PM2.5 ranged from 3.58 to 786 ng L-1, 0.72 to 12.3 ng g-1, 0.73 to 6.60 ng g-1, and 93.9 to 255 pg m-3, respectively, with mean concentrations of 149 ng L-1, 4.70 ng g-1, 4.31 ng g-1, and 156 pg m-3. Perfluorooctanoic acid (PFOA) was the dominant contaminant in water, soil, and sediment, and perfluoropentanoic acid (PFPeA) was the dominant contaminant in PM2.5. Hexafluoropropylene oxide-dimer acid (HFPO-DA) and 6 : 2 chlorinated polyfluorinated ether sulfonate (6 : 2 Cl-PFESA), as substitutes for PFOA and perfluorooctane sulfonate (PFOS), were detected, indicating the gradual replacement of traditional PFOA and PFOS in this area. Perfluoro-3,6-dioxaheptanoic acid (NFDHA), as a component of the aqueous film-forming foam FN-3, was first detected in this area. Short-chain PFASs were mainly distributed in water and PM2.5, while long-chain PFASs were distributed in the solid phase, such as soil, sediment, and PM2.5. Based on principal component analysis (PCA), the major PFAS sources were emulsifiers from fluorine polymerization and surface-active agents from the textile, papermaking, leather, and other industries. In addition, correlation analysis showed that water was the main source and transport pathway of short-chain perfluoroalkyl carboxylic acid (PFCA), HFPO-DA, and NFDHA in this area, while the atmosphere combined with PM2.5 was the main transport pathway for both short- and long-chain PFCAs, PFOS, and 6 : 2 Cl-PFESA.

Dataset Information

Occurrence and Distribution of Per- and Polyfluoroalkyl Substances from Multi-Industry Sources to Water, Sediments and Plants along Nairobi River Basin, Kenya.

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