Search

We analyzed per- and polyfluoroalkyl substances (PFAS) in aqueous film-forming foams (AFFFs) used to extinguish a major fire in a petrochemical terminal from the Port of Santos (Brazil). Eight AFFFs from seven known commercial brands and one unknown sample (AFFF-1 to AFFF-8) were evaluated. 17 PFAS were identified and quantified using high performance liquid chromatography (LC/MS). The concentrations of Σ17 PFAS in the AFFFs ranged from 500 to 9000 ng/g, with prevalence of short chain PFAS (~85 %), followed by long chain PFAS. Perfluorooctane sulfonic acid (PFOS) and perfluorooctanoic acid (PFOA), included in the global treaty of the Stockholm Convention, were also detected. We estimated that at least 635.96 g of PFAS were introduced in the estuary, representing a massive input of these substances. This investigation reports the PFAS composition of AFFFs used in firefighting in the GRULAC Region (Group of Latin American and Caribbean countries)., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Air-sea exchange of POPs and PAHs was assessed in Concepción Bay during January, summer 2015. Results showed low levels, in air and water, for POPs (1-20 pg m -3 , and 6-50 pg L -1 , respectively) and for ΣPAHs (1-2 ng m -3 and 1-2 ng L -1 , respectively). The highest levels were found for PBDEs (200-20,000 pg L -1 ) in the water samples (3-fold times higher than PCBs and OCP) and PBDE209 accounted for 90% of total ΣPBDEs. Air-sea exchange fluxes (ng m -2  d -1 ) were low in general, with exception of PBDEs showing values up to 40,000 ng m -2  d -1 . Net deposition was found for PAHs, HCB and some PBDEs; while, BDE99, and BDE100 showed net volatilization. These findings contribute with new data of diffusive air-sea exchange on the southern hemisphere Pacific coast., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Perfluorinated alkyl substances (PFASs) were determined in marine plastic litter (MPL) on six beaches of central Chile. MPL was characterized physically and chemically, showing an abundance of macroplastic (size >2.5 cm). The polypropylene (PP) (47%) was the predominant polymer found. The Desembocadura beach, located at the mouth of the Biobio River, recorded the highest abundance of MPL (3.7 items m -2 ). PFAS detected (n = 15/21) ranged from 279 to 1211 pg g -1 and accounted for MeFOSE (46%) > PFHxS (14%) > PFPA (11%) > PFBS (6%) > PFOA (4%) and > PFOS (4%). Long-chain PFAS were prevalent, which can be metabolically degraded into PFOS (new POPs). This study i) highlights the need to further investigate the occurrence of chemicals in the MPL to reduce their impact on the environment; and ii) points out the need to improve future coastal management strategies for the elimination of solid waste along the coast of the country., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

In this study, we characterized plastic debris (PD) found on beaches from Concepción Bay in central Chile during spring 2017 and summer 2018. The identification of polymers was carried out using FT-IR. Persistent organic pollutants (POPs) were extracted with hexane using an ultrasonic bath and further quantified through GC-MS. The highest abundance of PD was obtained during the summer (4.1 ± 3.7 items/m 2 ), with the most common size range between 2.5 and 10 cm (42%) and the most frequent shape were plastic fragments (44%). FT-IR analysis showed that polypropylene was the most recurrent plastic polymer found. The ∑10PBDEs ranged from 2.1 to 1300 ng/g in spring 2017 and 392 to 3177 ng/g in summer 2018. ∑7PCBs ranged from 0.9 to 93 ng/g during the spring 2017 and 0.3 to 4.5 ng/g for summer 2018. This study is the first with information on POPs occurrence in the plastic debris of central Chile., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Plastic resin pellets were collected from coastal areas (n = 7) of central Chile. Pellets were analyzed using Fourier-transform infrared spectroscopy for polymer identification and gas chromatography-mass spectrometry for Persistent Organic Pollutants (POPs) determination. Screened compounds were PBDEs (n = 10), PCBs (n = 7), and OCPs (n = 13). Pellets were only found at Lenga Beach (San Vicente Bay), which is likely influenced by the presence of industrial activities in the surrounding coastal area. The diameter of the pellets was 4.0 ± 0.6 cm (n = 370), the color varied from white (32%) to yellowing (68%), and the most prevalent polymer identified was high-density polyethylene (99%). POPs concentrations (ng/g-pellet) ranged from 10 to 133 for Ʃ10PBDEs, from 3 to 60 for Ʃ7PCBs and between 0.1 and 7 for DDTs. Levels of POPs are consistent with other investigations around the world and highlight the sorbtion capacity of plastics resin pellets, and consequently transport of POPs into coastal environments., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2019. Published by Elsevier Ltd.)

In this study we have identified and characterized microplastic particles (MPs) found in six fish species of commercial importance in central Chile. The fish species belong to different trophic levels and were obtained from the oceanic and coastal habitats. To analyze MPs, the fish gastrointestinal content was extracted, analyzed and characterized using a microscopy equipped with Fourier-transform infrared spectroscopy (FT-IR). The MPs found in fish samples were mainly constituted by red microfibers (70-100%) with sizes ranging between 176 and 2842 μm. Polyester, polyethylene (PE) and polyethylene terephthalate (PET) were identified as the prevalent polymers detected. The coastal species showed the presence of microfibers with a higher size and abundance (71%) compared to oceanic species (29%), suggesting there is a greater exposure risk. These findings are consistent with results found in other investigations worldwide. However, further research is still needed to accurately establish the potential exposure risk for the public consuming these fish and the impact of MPs in the Chilean fishery activities., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Pharmaceuticals, personal care products (PPCPs), and artificial sweeteners (ASWs) are contaminants of emerging concern commonly found in the aquatic environments. In India, studies reporting environmental occurrence of these contaminants are scarce. In this study, we investigated the occurrence and distribution of 15 PPCPs and five ASWs in the river and groundwater (used untreated as drinking water) at several sites along the Ganges River. Based on the measured groundwater concentrations, we estimated the life-long human health risk from exposure to PPCPs through drinking. In addition, we estimated the risk of exposure to PPCPs and ASWs in the river water for aquatic organisms. The sum of detected PPCPs in the river water ranged between 54.7-826 ng/L, with higher concentrations in the severely anthropogenically influenced middle and lower reaches of the Ganges. The highest concentration among the PPCPs in the river water was of caffeine (743 ng/L). The sum of detected ASWs in river water ranged between 0.2-102 ng/L. Similar to PPCPs, the sum of ASWs in the river water was higher in the middle and lower reaches of the Ganges. In groundwater, the sum of detected PPCPs ranged between 34-293 ng/L, whereas of ASWs ranged between 0.5-25 ng/L. Negligible risk for humans was estimated from PPCPs in the drinking groundwater sources along the Ganges River, whereas moderate risks to PPCPs and ASWs (namely: caffeine, sulfamethoxazole, triclocarban, triclosan, and sucralose) were estimated for aquatic organisms in the Ganges River., (Copyright © 2018 Elsevier B.V. All rights reserved.)

Two groups of perfluorined compounds (PFCs), i.e. perfluoroalkyl sulfonates (PFASs) and perfluoroalkyl carboxylates (PFCAs) were analysed during a period of 1 year in monthly collected riverbed sediment samples from five sampling sites in an industrial region in Morava River catchment in Czech Republic. Levels of PFCs determined in sediment samples were up to 6.8 μg kg(-1) of dry weight. Among PFCs analysed, mainly short-chain PFASs (C6 to C8) including PFOS were found in sediment samples and their levels were similar to those found in comparable river basins in other parts of Europe. Concentrations of PFCs were correlated with organic carbon content and their variations were mainly correlated by high flow events on Morava River and its tributaries. The changes in PFC concentrations were induced by displacing of PFCs containing particles to the river sediment during these elevated flow events., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Riverine sediments, collected on a monthly basis during a period of one year, from five sites in a mixed land use region of the Czech Republic were analysed for chlorinated and brominated persistent organic pollutants (POPs). The region is located in the upper catchment of the Danube River. The POPs concentrations were as follows: 11-930 pg g(-1) polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDDs/Fs), 170-980 pg g(-1) dioxin-like polychlorinated biphenyls (dl-PCBs), 34-13,700 pg g(-1) polychlorinated naphthalenes (PCNs), 5.7-29,200 pg g(-1) polybrominated diphenylethers (PBDEs) and 0.21-351 ng g(-1) hexabromocyclododecanes (HBCDs). Concentrations expressed as toxic equivalents (TEQs), for PCDD/F+dl-PCB+PCN (TEQPCDD/F+dl-PCB+PCN) ranged from 0.37 to 19 pg g(-1). The results revealed a clear spatial separation between sites based on concentration and congener profile. There were also some obvious temporal patterns of selected POPs, which were related to river flow (seasonality) and organic carbon (TOC) of the sediment. Potential sources of POPs include local municipalities (flame retardants), some diffuse sources (PCNs and PCDDs/Fs) and potential point sources (PBDEs). Risk assessment based on risk quotients (RQ) revealed limited to medium ecological risk from PBDEs. TEQPCDD/F+dl-PCB+PCN were low relative to other European rivers, hence the risk to aquatic organisms was considered to be low. PCNs contributed significantly to overall TEQ in several cases., (Copyright © 2015 Elsevier Ltd. All rights reserved.)

PBDEs (10 congeners) were analyzed using GC-MS in superficial sediments and organisms of the Concepción Bay after the 2010 Tsunami. From all congeners analyzed PBDE-47, -99, -100 and -209 were the most frequently detected. Concentrations (ngg(-1) d.w.) in sediments for ΣPBDE-47, -99, -100 were low (0.02-0.09). However, PBDE-209 showed significantly higher values ∼20ngg(-1) d.w. This result were ∼10 times lower than those reported in a previous study of the 2010 Tsunami. The high result might be influenced by the massive urban debris dragged by the 2010 Tsunami. In organisms, concentrations of PBDE-47, -99, -100 (∼0.4ngg(-1) d.w.) were higher than those found in sediments (∼0.04ngg(-1) d.w.). Differences in PBDE pattern were also observed between different levels of the trophic food chain (primary and secondary consumers). This is the first attempt to assess the current status of Concepción Bay after the 2010 Tsunami., (Copyright © 2015 Elsevier Ltd. All rights reserved.)

Dissolved waterborne polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) were assessed over a period of one year at five sampling sites in a model industrial region in the Czech Republic using silicone rubber passive samplers. The spatial variability of POPs in the studied region in water was small and diffusive pollution sources predominate. Concentrations of the most volatile PAHs decreased with increasing water temperature in the whole region, which reflects the seasonality in atmospheric deposition. The dissolved concentrations of more hydrophobic PAHs, PCBs and OCPs in and downstream the industrial zone are related to desorption from suspended particles. Upstream the industrial area, a positive correlation of dissolved and particle-bound contamination was observed only for DDT metabolites and hexachlorobenzene. Calculated fugacities in water and bottom sediment indicated a fair degree of equilibrium between these compartments for OCPs and PCBs, whereas sediment represented a potential source of PAHs., (Copyright © 2012 Elsevier Ltd. All rights reserved.)

River sediments are a dynamic system, especially in areas where floods occur frequently. In the present study, an integrative approach is used to investigate the seasonal and spatial dynamics of contamination of sediments from a regularly flooded industrial area in the Czech Republic, which presents a suitable model ecosystem for pollutant distribution research at a regional level. Surface sediments were sampled repeatedly to represent two different hydrological situations: spring (after the peak of high flow) and autumn (after longer period of low flow). Samples were characterized for abiotic parameters and concentrations of priority organic pollutants. Toxicity was assessed by Microtox test; genotoxicity by SOS-chromotest and green fluorescent protein (GFP)-yeast test; and the presence of compounds with specific mode of action by in vitro bioassays for dioxin-like activity, anti-/androgenicity, and anti-/estrogenicity. Distribution of organic contaminants varied among regions and seasonally. Although the results of Microtox and genotoxicity tests were relatively inconclusive, all other specific bioassays led to statistically significant regional and seasonal differences in profiles and allowed clear separation of upstream and downstream regions. The outcomes of these bioassays indicated an association with concentrations of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) as master variables. There were significant interrelations among dioxin-like activity, antiandrogenicity and content of organic carbon, clay, and concentration of PAHs and PCBs, which documents the significance of abiotic factors in accumulation of pollutants. The study demonstrates the strength of the specific bioassays in indicating the changes in contamination and emphasizes the crucial role of a well-designed sampling plan, in which both spatial and temporal dynamics should be taken into account, for the correct interpretations of information in risk assessments.

The present study represents the first broader evaluation of the rapid 30-s kinetic bioluminescence assay with Vibrio fisheri (microplate format modification) for contact toxicity testing of whole sediments. The present study focused on river sediments from the Morava River basin, Czech Republic, repeatedly sampled during 2005 to 2006 and analyzed for geological and geochemical parameters, content of toxic metals, major organic pollutants, and toxicity. High natural variation in toxicity (50% inhibitory concentration [IC50] values ranging from 0.8 to >80 mg sediment dry wt/ml) was found (among different sampling periods and years, among sites), and this could be related to the sediment dynamics affected by spring high flows and summer droughts. From the 46 sediment descriptors, exchangeable protons (H(+)) was the only parameter that consistently correlated with toxicity. Three other descriptors (i.e., content of organic carbon plus two parameters from the detailed silicate analysis of sediments: percentage of SO(3) representing total sulfur content, structural water H(2)O+) also significantly correlated with toxicity. There were only minor and variable correlations with contamination. We propose sediment safety guideline categories for the V. fisheri kinetic test with severe toxicity threshold of IC50 < 1 mg dry wt/ml. Although sediments are considered a rather stable matrix in comparison with river water, we confirmed high variability and dynamics that should be reflected in monitoring plans and field studies.

A multimedia sampling of ambient air, wet deposition, surface water, sediment, soil and biota has been performed at Kosetice background observatory in the southern Czech Republic since 1988. An integrated monitoring approach was applied to assess the current state, anthropogenic impacts, and possible future changes of terrestrial and freshwater environments. Average PCB concentrations in the individual matrices calculated from ten years of sampling on multiple sites varied between 2 ng g(-1) in sediment and 7 ng g(-1) in soil or moss. DDT concentrations were lower in moss and needles (2 ng g(-1) and 4 ng g(-1), respectively) than in sediment (11 ng g(-1)) and soil (20 ng g(-1)), while the HCH level was higher in moss and needles (5 ng g(-1) and 6 ng g(-1), respectively) than in soil or sediment (1 ng g(-1) and 2 ng g(-1), respectively). The highest average level of PAHs was found in soil (600 ng g(-1)), while it was lower in needles (230 ng g(-1)), moss (210 ng g(-1)) or sediment (210 ng g(-1)). Time related trends of concentration levels of persistent organic pollutants in all matrices were investigated. Moss and needle trend patterns resembled those of the ambient air, showing a slight concentration decrease of all compounds, except for hexachlorobenzene. The soil, water and sediment concentrations showed a similar decrease of PAHs, PCBs, and HCHs, but there was no clear trend for DDTs and HCB.

Photolysis of 2- and 4-chlorophenol samples in water ice of the initial concentrations 10(-7) to 10(-2) mol L(-1) is reported. Major phototransformations appeared to be based on the coupling reactions due to chlorophenol aggregation at the grain boundaries of the polycrystalline state. The main products, chlorobiphenyldiols, belong to the family of phenolic halogenated compounds (such as hydroxylated polychlorobiphenyls) that are known xenobiotics found in nature. No photosolvolysis products, that is products from intermolecular reactions between organic and water molecules, were observed at temperatures below -10 degrees C. Raising the temperature to -5 degrees C caused a moderate photosolvolytic activity in the case of 4-chlorophenol (formation of hydroquinone), in contrast to 2-chlorophenol which was almost exclusively transformed into pyrocatechol. It is suggested that photosolvolysis above this temperature occurs in a liquid or quasi-liquid layer that covers the ice crystal surfaces. The results support our model in which significant amounts of some persistent, bioaccumulative, and toxic compounds may be generated by photochemistry of primary pollutants in cold ecosystems and in the upper atmosphere, and may be subsequently released to the environment.