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dc.contributor.authorMasteling, R. P.por
dc.contributor.authorCastro, Bruno B.por
dc.contributor.authorAntunes, S. C.por
dc.contributor.authorNunes, B.por
dc.date.accessioned2017-12-07T18:02:53Z-
dc.date.issued2016-
dc.identifier.citationMasteling, R. P. P., Castro, B. B. B., Antunes, S. C. C. and Nunes, B. (2016). Whole-organism and biomarker endpoints in Daphnia magna show uncoupling of oxidative stress and endocrine disruption in phenolic derivatives. Ecotoxicology and Environmental Safety 134, 64–71. doi:10.1016/j.ecoenv.2016.08.012.por
dc.identifier.issn0147-6513por
dc.identifier.urihttps://hdl.handle.net/1822/48109-
dc.description.abstractDuring the past century, the amount of chemicals released into water bodies has increased, with particular emphasis being attributed to xenobiotics with endocrine disruption properties and/or pro-oxidant effects. Among these, it is possible to identify a specific chemical class, alkylphenols, which are of widespread use, and include a variety of chemicals with multiple uses. Bisphenol A is an important chemical used in industrial production of plastics, and has been extensively described as an endocrine disruptor. Paracetamol is a pharmaceutical compound used in human medicine, known for its therapeutic action but also for its evident pro-oxidant features. Additionally, previous studies have suggested that paracetamol may also exert endocrine disruption. The main goal of this study was to assess the effects of both paracetamol and bisphenol A as endocrine disruptors, and as promoters of oxidative stress and damage, on the freshwater microcrustacean Daphnia magna. The obtained results showed that bisphenol A was capable of altering population traits of exposed organisms, by impairing molting. On the contrary, paracetamol was not causative of any significant change in this parameter, despite having caused extensive oxidative stress.por
dc.description.sponsorshipBruno Nunes was hired under the programme Investigador FCT, co-funded by the Human Potential Operational Programme (National Strategic Reference Framework 2007-2013) and European Social Fund (European Union (EU)). This work was supported by the strategic programme UID/BIA/04050/2013 (CBMA: POCI-01-0145-FEDER-007569), UID/Multi/04423/2013 (CIIMAR) and UID/AMB/50017/2013 (CESAM), funded by national funds through the FCT I.P. and by the ERDF through the COMPETE2020 - Programa Operacional Competitividade e Internacionalizacao (POO).por
dc.language.isoengpor
dc.publisherAcademic Presspor
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147364/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147268/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147273/PTpor
dc.rightsrestrictedAccesspor
dc.subjectParacetamolpor
dc.subjectBisphenol Apor
dc.subjectOxidative stresspor
dc.subjectAcute toxicitypor
dc.subjectSub-chronic effectspor
dc.titleWhole-organism and biomarker endpoints in Daphnia magna show uncoupling of oxidative stress and endocrine disruption in phenolic derivativespor
dc.typearticlepor
dc.peerreviewedyespor
dc.commentsDireitos de autor com a Editorapor
oaire.citationStartPage64por
oaire.citationEndPage71por
oaire.citationVolume134por
dc.identifier.doi10.1016/j.ecoenv.2016.08.012por
dc.subject.fosCiências Naturais::Ciências Biológicaspor
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersionpor
dc.subject.wosScience & Technologypor
sdum.journalEcotoxicology and Environmental Safetypor
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