Publications by authors named "Elisa Rojo-Nieto"

This paper presents an approach to apply aquatic passive sampling (PS) in regulatory chemical water quality monitoring in Europe. Absorption-based passive sampling is well developed and suitable for the sampling of hydrophobic chemicals, some of which are European Water Framework Directive priority substances with Environmental Quality Standards (EQS) derived for biota. Considering a chemical activity approach to chemical risk assessment, we propose equilibrium concentration in lipids (from passive water sampling) as a reference value for measured concentrations in biota.

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We applied passive equilibrium sampling using silicone-based chemometers to nine biota species, sediment, and water in a multimedia aquatic ecosystem. They allowed for direct comparison of the concentration of regulated and emerging hydrophobic organic compounds in the silicone across species as well as the comparison of biota with sediments and water. We derived chemometer-based trophic magnification factors (TMFs) of diverse compounds that agreed with the traditionally derived TMFs.

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Plastics are produced with a staggering array of chemical compounds, with many being known to possess hazardous properties, and others lacking comprehensive hazard data. Furthermore, non-intentionally added substances can contaminate plastics at various stages of their lifecycle, resulting in recycled materials containing an unknown number of chemical compounds at unknown concentrations. While some national and regional regulations exist for permissible concentrations of hazardous chemicals in specific plastic products, less than 1 % of plastics chemicals are subject to international regulation [1].

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The present study complements work on mixture effects measured with bioassays of passive equilibrium sampling extracts using the silicone polydimethylsiloxane (PDMS) in organs from marine mammals with chemical profiling. Blubber, liver, kidney and brain tissues of harbor porpoise (), harbor seal (), ringed seal () and orca () from the North and Baltic Seas were investigated. We analyzed 117 chemicals including legacy and emerging contaminants using gas chromatography-high resolution mass spectrometry and quantified 70 of those chemicals in at least one sample.

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We propose novel chemometers - passive equilibrium samplers of, , silicone - as an integrative tool for the assessment of hydrophobic organic compounds in multimedia environments. The traditional way of assessing levels of organic pollutants across different environmental compartments is to compare the chemical concentration normalized to the major sorptive phase in two or more media. These sorptive phases for hydrophobic organic compounds differ between compartments, , lipids in biota and organic carbon in sediments.

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Background: Bioaccumulation of hydrophobic organic compounds (HOCs) along freshwater food chains is a major environmental concern as top predators in food webs are relevant for human consumption. To characterize and manage the associated risks, considerable numbers of organisms are sampled regularly for monitoring purposes. However, ethical and financial issues call for an alternative, more generic and more robust approach for assessing the internal exposure of fish that circumvents large variability in biota sampling due to interindividual differences.

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Contaminant analysis in biota extracts can be hampered by matrix interferences caused by, for example, co-extracted lipids that compromise the quality of the analytical data and require frequent maintenance of the analytical instruments. In the present study, using gas chromatography coupled to high resolution mass spectrometry (GC-HRMS), we aimed to develop and validate a straightforward, robust, and reproducible cleanup method with acceptable recoveries for diverse compound classes with a wide range of physicochemical properties representative of pollutant screening in biota extracts. We compared Oasis PRiME HLB cartridges, Agilent Captiva EMR-Lipid cartridges, and "Freeze-Out" with salmon lipids spiked with 113 target chemicals.

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We described in 2017 how weathering plastic litter in the marine environment fulfils two of three criteria to impose a planetary boundary threat related to "chemical pollution and the release of novel entities": (1) planetary-scale exposure, which (2) is not readily reversible. Whether marine plastics meet the third criterion, (3) eliciting a disruptive impact on vital earth system processes, was uncertain. Since then, several important discoveries have been made to motivate a re-evaluation.

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Passive equilibrium sampling using polymer samplers in lean tissue is one of the current challenges in assessing bioaccumulation and biomagnification due to the long time needed to reach equilibrium. Despite recent progress achieved by rolling pieces of intact fish fillet with sheets of silicone, there is still a need for a passive sampling method for homogenates that achieves equilibrium before tissue decay starts. In this work, a new approach for relocation of silicone passive samplers in homogenates of lean fish was established for three homogenates with lipid contents varying from 1.

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Stable isotope analysis (δC and δN from liver and muscle) was used to assess trophic relationships between Atlantic bluefin tuna (ABFT) (Thunnus thynnus) and striped dolphin (SC) (Stenella coeruleoalba) in the Strait of Gibraltar (SoG). δN values from ABFT muscle and liver tissues were significantly different from those of dolphin samples, but no for δC values. Diet estimation by MixSIAR models from muscle and liver revealed that ABFT fed mainly on squids (Todaropsis eblanae and Illex coindetii).

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Dolphins are considered sentinel species in the marine environment. The Strait of Gibraltar is the only passage between the Mediterranean Sea and the Atlantic Ocean, being the transitional region which connects these two basins and one of the most important routes of cetacean migration worldwide. In this work, eight trace elements (TE) were studied in 45 samples of liver, kidney and muscle, from 15 specimens stranded in this study area.

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In soils and sediments contaminated by Hydrophobic Organic Compounds (HOCs), the total concentrations are less indicative of potential exposure and distribution than the associated freely dissolved concentrations (Cfree) or chemical activity. Therefore, these two parameters are increasingly used to assess sediment contamination with regard to their (1) partitioning into the water column, (2) bioaccumulation and (3) baseline toxic potential. In this work, sediments from a chronically polluted coastal area, with similar total PAH concentrations, were studied using PDMS coated glass jars (obtaining Cfree(SW) and chemical activity) to predict baseline toxicity and potential bioaccumulation from these sediments.

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This paper describes a study of the occurrence, levels and temporal evolution of PAHs in a bay characterized by persistent chronic impacts. A total of 40 samples, 20 of sediment and 20 of water, were taken at each of five different stations, in four sampling campaigns. Analyses of pollutants have been made using GC-MS.

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