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dc.contributor.authorHansen, Bjørn Henrik
dc.contributor.authorNordtug, Trond
dc.contributor.authorFarkas, Julia
dc.contributor.authorKhan, Essa Ahsan
dc.contributor.authorOteri, Erika
dc.contributor.authorKvæstad, Bjarne
dc.contributor.authorFaksness, Liv-Guri
dc.contributor.authorDaling, Per Snorre
dc.contributor.authorArukwe, Augustine
dc.date.accessioned2021-09-22T06:55:20Z
dc.date.available2021-09-22T06:55:20Z
dc.date.created2021-07-14T16:24:44Z
dc.date.issued2021
dc.identifier.citationAquatic Toxicology. 2021, 237 1-12.en_US
dc.identifier.issn0166-445X
dc.identifier.urihttps://hdl.handle.net/11250/2780215
dc.description.abstractDue to the heavy fuel oil (HFO) ban in Arctic maritime transport and new legislations restricting the sulphur content of fuel oils, new fuel oil types are continuously developed. However, the potential impacts of these new fuel oil types on marine ecosystems during accidental spills are largely unknown. In this study, we studied the toxicity of three marine fuel oils (two marine gas oils with low sulphur contents and a heavy fuel oil) in early life stages of cod (Gadus morhua). Embryos were exposed for 4 days to water-soluble fractions of fuel oils at concentrations ranging from 4.1 - 128.3 µg TPAH/L, followed by recovery in clean seawater until 17 days post fertilization. Exposure to all three fuel oils resulted in developmental toxicity, including severe morphological changes, deformations and cardiotoxicity. To assess underlying molecular mechanisms, we studied fuel oil-mediated activation of aryl hydrocarbon receptor (Ahr) gene battery and genes related to cardiovascular, angiogenesis and osteogenesis pathways. Overall, our results suggest comparable mechanisms of toxicity for the three fuel oils. All fuel oils caused concentration-dependant increases of cyp1a mRNA which paralleled ahrr, but not ahr1b transcript expression. On the angiogenesis and osteogenesis pathways, fuel oils produced concentration-specific transcriptional effects that were either increasing or decreasing, compared to control embryos. Based on the observed toxic responses, toxicity threshold values were estimated for individual endpoints to assess the most sensitive molecular and physiological effects, suggesting that unresolved petrogenic components may be significant contributors to the observed toxicity.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleToxicity and developmental effects of Arctic fuel oil types on early life stages of Atlantic cod (Gadus morhua)en_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1-12en_US
dc.source.volume237en_US
dc.source.journalAquatic Toxicologyen_US
dc.identifier.doi10.1016/j.aquatox.2021.105881
dc.identifier.cristin1921771
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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