Intracellular microcystins degradation and acute toxicity decrease towards Daphnia similis by low electron-beam irradiation doses

dc.contributor.authorSILVA, THALITA T.pt_BR
dc.contributor.authorJACINAVICIUS, FERNANDA R.pt_BR
dc.contributor.authorPINTO, ERNANIpt_BR
dc.contributor.authorBORRELY, SUELI I.pt_BR
dc.coverageInternacional
dc.date.accessioned2023-06-23T17:50:25Z
dc.date.available2023-06-23T17:50:25Z
dc.date.issued2023pt_BR
dc.description.abstractIonizing radiation has attracted attention due to its ability to inhibit pathogens and microorganisms, with low doses reported as being able to degrade cyanotoxins and inhibit toxic cyanobacteria growth. In this context, the aim of the present study was to investigate how electron beam irradiation (EBI) applied at doses between 1 and 10 kGy affect intracellular and extracellular microcystin variants. Effects on M. aeruginosa culture recovery, as well as changes in physico-chemical cyanobacterial suspension parameters and water quality alterations were assessed through ecotoxicity assays. The findings indicate that doses over 2 kGy may are lethal to M. aeruginosa even at 48 h post-irradiation. Concerning physico-chemical parameters, exposure to 2–5 kGy doses decrease pH values and later stabilizing. At least 50 % of intracellular MC led to significant degradation of all variants at 3 kGy. No acute toxicity effects were observed in Daphnia similis exposed to sample supernatants. Statistically significant differences were observed when cladocerans were exposed to M. aeruginosa cells treated with EBI doses ranging from 3 to 10 kGy compared to non-treated cyanobacterial suspensions. These findings suggest that low EBI radiation doses are suitable for the control of toxic cyanobacteria in water treatment processes, providing a less toxic environment compared to non-treated solutions.pt_BR
dc.description.sponsorshipInternational Atomic Energy Agency (IAEA)pt_BR
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)pt_BR
dc.description.sponsorshipIDIAEA: RC 23033pt_BR
dc.description.sponsorshipIDCAPES: 2018/ 1.1065.9.1pt_BR
dc.format.extent1-7pt_BR
dc.identifier.citationSILVA, THALITA T.; JACINAVICIUS, FERNANDA R.; PINTO, ERNANI; BORRELY, SUELI I. Intracellular microcystins degradation and acute toxicity decrease towards Daphnia similis by low electron-beam irradiation doses. <b>Algal Research</b>, v. 72, p. 1-7, 2023. DOI: <a href="https://dx.doi.org/10.1016/j.algal.2023.103086">10.1016/j.algal.2023.103086</a>. Disponível em: http://repositorio.ipen.br/handle/123456789/34078.
dc.identifier.doi10.1016/j.algal.2023.103086pt_BR
dc.identifier.issn2211-9264
dc.identifier.orcidhttps://orcid.org/0000-0002-9692-5539
dc.identifier.percentilfi82.5
dc.identifier.percentilfiCiteScore92.00
dc.identifier.urihttp://repositorio.ipen.br/handle/123456789/34078
dc.identifier.vol72pt_BR
dc.relation.ispartofAlgal Research
dc.rightsopenAccesspt_BR
dc.subjectdaphnia
dc.subjecttoxicity
dc.subjectcyanobacteria
dc.subjectelectron beams
dc.subjectirradiation
dc.subjectionizing radiations
dc.subjectoxidation
dc.titleIntracellular microcystins degradation and acute toxicity decrease towards Daphnia similis by low electron-beam irradiation dosespt_BR
dc.typeArtigo de periódicopt_BR
dspace.entity.typePublication
ipen.autorSUELI IVONE BORRELY
ipen.autorTHALITA TIEKO SILVA
ipen.codigoautor150
ipen.codigoautor15126
ipen.contributor.ipenauthorSUELI IVONE BORRELY
ipen.contributor.ipenauthorTHALITA TIEKO SILVA
ipen.date.recebimento23-06
ipen.identifier.fi4.6
ipen.identifier.fiCiteScore9.4
ipen.identifier.ipendoc29712
ipen.identifier.iwosWoSpt_BR
ipen.identifier.ods6
ipen.range.fi4.500 - 5.999
ipen.range.percentilfi75.00 - 100.00
ipen.type.genreArtigo
relation.isAuthorOfPublication76171e20-c8ac-475f-9006-27402113c92f
relation.isAuthorOfPublication3cae4a76-5492-456b-9c40-409024c0ea88
relation.isAuthorOfPublication.latestForDiscovery3cae4a76-5492-456b-9c40-409024c0ea88
sigepi.autor.atividadeBORRELY, SUELI I.:150:220:Npt_BR
sigepi.autor.atividadeSILVA, THALITA T.:15126:220:Spt_BR

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