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dc.contributor.authorAragão, Marianna Correia-
dc.contributor.authorReis, Kelly Cristina dos-
dc.contributor.authorRocha, Maria Aparecida Melo-
dc.contributor.authorGuedes, Dayvson de Oliveira-
dc.contributor.authorSantos, Eduardo Costa dos-
dc.contributor.authorCapelo Neto, José-
dc.date.accessioned2023-07-07T12:46:53Z-
dc.date.available2023-07-07T12:46:53Z-
dc.date.issued2021-
dc.identifier.citationARAGÃO, Marianna Correia; REIS, Kelly Cristina dos; ROCHA, Maria Aparecida Melo; GUEDES, Dayvson de Oliveira; SANTOS, Eduardo Costa dos; CAPELO-NETO, Jose. Removal of Dolichospermum circinale, Microcystis aeruginosa, and their metabolites using hydrogen peroxide and visible light. Aquatic Toxicology, [S. l.], v. 232, n. 105735, p. 1-7, 2021.pt_BR
dc.identifier.issn1879-1514-
dc.identifier.urihttp://www.repositorio.ufc.br/handle/riufc/73394-
dc.description.abstractFrequent cyanobacterial blooms in reservoirs used for human supply increase the risk of noxious secondary metabolites, endangering human health and ecological balance, and requiring constant monitoring by water companies. Although hydrogen peroxide (H2O2) has been widely reported as an effective agent for the control of cyanobacteria, being Microcystis aeruginosa one of the most studied species, very limited data is available on its effects over Dolichospermum circinale. Therefore, this study aimed to evaluate the impact of H2O2 on D. circinale and comparing it to the effects over the M. aeruginosa. The treatment was performed in cyanobacterial cultures with the application of 2 and 5 mg L−1 of H2O2 under visible light. To measure the impact of the treatment, intact cells were counted and cell re-growth monitored. Geosmin and microcystin, cell pigments, color, and organic matter in water were also analyzed during the treatment. The results showed that even the smallest H2O2 concentration (2 mg L−1) was able to completely remove D. circinale cells. Although M. aeruginosa could only be completely removed using 5 mg L−1, the few cells remaining after the application of 2 mg L−1 were not viable and did not re-grew after 15 days. Total microcystin concentration increased after M. aeruginosa was exposed to H2O2, suggesting that oxidative stress may increase the detection of this metabolite when the cells are lysed. While 2 mg L−1 was able to significantly decrease total geosmin, the addition of 5 mg L−1 did not improve removal. Chlorophyll-a was readily degraded after cell rupture but the same did not happen to phycocyanin, demonstrating its high resilience to this oxidant. Color and organic matter increased for the M. aeruginosa but decreased for the D. circinale suspension, probably because the higher concentration of the M. aeruginosa yielded more extracellular content to the water which was not able to be degraded by the amount of H2O2 applied.pt_BR
dc.language.isoenpt_BR
dc.publisherAquatic Toxicologypt_BR
dc.rightsAcesso Abertopt_BR
dc.subjectAdvanced oxidation processespt_BR
dc.subjectPigmentspt_BR
dc.subjectGeosminpt_BR
dc.subjectMicrocystinspt_BR
dc.titleRemoval of Dolichospermum circinale, Microcystis aeruginosa, and their metabolites using hydrogen peroxide and visible lightpt_BR
dc.typeArtigo de Periódicopt_BR
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