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Auteur Beiras, R.; Bellas, J.; Cachot, J.; Cormier, B.; Cousin, X.; Engwall, M.; Gambardella, C.; Garaventa, F.; Keiter, S.; Le Bihanic, F.; Lopez-Ibanez, S.; Piazza, V.; Rial, D.; Tato, T.; Vidal-Linan, L. doi  openurl
  Titre Ingestion and contact with polyethylene microplastics does not cause acute toxicity on marine zooplankton Type Article scientifique
  Année 2018 Publication (up) Revue Abrégée J. Hazard. Mater.  
  Volume 360 Numéro Pages 452-460  
  Mots-Clés Benzophenone-3; coastal waters; ecotoxicological evaluation; Embryo-larval bioassays; environmental risk-assessment; isochrysis-galbana; larval development; Marine litter; Marine zooplankton; mytilus-galloprovincialis; organic pollutants; paracentrotus-lividus; plastic debris; Polyethylene; uv-filters  
  Résumé Toxicity of polyethylene microplastics (PE-MP) of size ranges similar to their natural food to zooplanktonic organisms representative of the main taxa present in marine plankton, including rotifers, copepods, bivalves, echinoderms and fish, was evaluated. Early life stages (ELS) were prioritized as testing models in order to maximize sensitivity. Treatments included particles spiked with benzophenone-3 (BP-3), a hydrophobic organic chemical used in cosmetics with direct input in coastal areas. Despite documented ingestion of both virgin and BP-3 spiked microplastics no acute toxicity was found at loads orders of magnitude above environmentally relevant concentrations on any of the invertebrate models. In fish tests some effects, including premature or reduced hatching, were observed after 12 d exposure at 10 mg L-1 of BP-3 spiked PE-MP. The results obtained do not support environmentally relevant risk of microplastics on marine zooplankton. Similar approaches testing more hydrophobic chemicals with higher acute toxicity are needed before these conclusions could be extended to other organic pollutants common in marine ecosystems. Therefore, the replacement of these polymers in consumer products must be carefully considered.  
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  Langue English Langue du Résumé Titre Original  
  Éditeur de collection Titre de collection Titre de collection Abrégé  
  Volume de collection Numéro de collection Edition  
  ISSN 0304-3894 ISBN Médium  
  Région Expédition Conférence  
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  Numéro d'Appel MARBEC @ alain.herve @ collection 2432  
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Auteur Cormier, B.; Batel, A.; Cachot, J.; Begout, M.-L.; Braunbeck, T.; Cousin, X.; Keiter, S.H. doi  openurl
  Titre Multi-Laboratory Hazard Assessment of Contaminated Microplastic Particles by Means of Enhanced Fish Embryo Test With the Zebrafish (Danio rerio) Type Article scientifique
  Année 2019 Publication (up) Revue Abrégée Front. Environ. Sci.  
  Volume 7 Numéro Pages 135  
  Mots-Clés aromatic-hydrocarbons pahs; benzo[a]pyrene; chronic dietary exposure; cyp1a; erod; fish embryotoxicity test (FET); fresh-water; gene-expression; hydrophobic organic-chemicals; marine-environment; oxybenzone; perfluorooctane sulfonate; plastic debris; resin pellets; risk-assessment; swimming behavior; uv-filters  
  Résumé As wide-spread pollutants in the marine environment, microplastics (MPs) have raised public concern about potential toxic effects in aquatic organisms, and, among others, MPs were suspected to act as a vector for organic pollutants to biota. The purpose of the present study was to investigate effects by three model pollutants, oxybenzone (BP3), benzo[a] pyrene (BaP), and perfluorooctane sulfonate (PFOS) adsorbed to polyethylene MPs on the basis of a standard assay, the acute fish embryo toxicity test (FET; OECD TG 236) with zebrafish (Danio rerio) supplemented by additional endpoints such as induction of ethoxyresorufin-O-deethylase (EROD) activity, modification of cyp1a gene transcription and changes in larval swimming behavior. FET assays were performed in three laboratories using slightly different husbandry and exposure conditions, which, however, were all fully compatible with the limits defined by OECD TG 236. This allowed for testing of potential changes in the FET assay due to protocol variations. The standard endpoints of the FET (acute embryotoxicity) did not reveal any acute toxicity for both virgin MPs and MPs spiked with BP3, BaP, and PFOS. With respect to sublethal endpoints, EROD activity was increased after exposure to MPs spiked with BP3 (3 h pulse) and MPs spiked with BaP (96 h continuous exposure). Cyp1a transcription was increased upon exposure to MPs spiked with BP3 or BaP. For the selected combination of MPs particles and contaminants, the basic FET proved not sensitive enough to reveal effects of (virgin and spiked) MPs. However, given that the FET can easily be supplemented by a broad variety of more subtle and sensitive endpoints, an enhanced FET protocol may provide a relevant approach with developmental stages of a vertebrate animal model, which is not protected by current EU animal welfare legislation (Directive EU 2010/63).  
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  Auteur institutionnel Thèse  
  Editeur Lieu de Publication Éditeur  
  Langue English Langue du Résumé Titre Original  
  Éditeur de collection Titre de collection Titre de collection Abrégé  
  Volume de collection Numéro de collection Edition  
  ISSN ISBN Médium  
  Région Expédition Conférence  
  Notes WOS:000486181200001 Approuvé pas de  
  Numéro d'Appel MARBEC @ isabelle.vidal-ayouba @ collection 2646  
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