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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/66555
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dc.contributor.authorVictor, Sandra R.-
dc.contributor.authorVieira, Paulo C.-
dc.contributor.authorFátima G F Da Silva, M.-
dc.contributor.authorCrisóstomo, Fernando R.-
dc.contributor.authorBueno, Fabiana C.-
dc.contributor.authorPagnocca, Fernando C.-
dc.contributor.authorFernandes, João B.-
dc.contributor.authorCorrea, Arlene G.-
dc.contributor.authorBueno, Odair C.-
dc.contributor.authorJosé A Hebling, M.-
dc.contributor.authorJr, Maurício Bacci-
dc.date.accessioned2014-05-27T11:20:17Z-
dc.date.accessioned2016-10-25T18:17:07Z-
dc.date.available2014-05-27T11:20:17Z-
dc.date.available2016-10-25T18:17:07Z-
dc.date.issued2001-07-20-
dc.identifierhttp://dx.doi.org/10.1002/ps.333-
dc.identifier.citationPest Management Science, v. 57, n. 7, p. 603-608, 2001.-
dc.identifier.issn1526-498X-
dc.identifier.urihttp://hdl.handle.net/11449/66555-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/66555-
dc.description.abstractThe development of Leucoagaricus gongylophorus, the fungus cultured by the leaf-cutting ant Atta sexdens was inhibited in vitro by synthetic compounds containing the piperonyl group. In addition, worker ants that were fed daily on an artificial diet to which these compounds were added had a higher mortality rate than the controls. The inhibition of the fungal growth increased with the size of the carbon side chain ranging from C1 through C8 and decreasing thereafter. 1-(3,4-Methylenedioxybenzyloxy)octane (compound 5) was the most active compound and inhibited the fungal development by 80% at a concentration of 15 μg m1-1. With worker ants the toxic effects started with compound 5 and increased with the number of carbons in the side chain. Thus, for the same concentration (100 μg m1-1) the mortality rates observed after 8 days of diet ingestion were 82%, 66% and 42%, for 1-(3,4-methylenedioxybenzyloxy)decane, 1-(3,4-methylenedioxybenzyloxy)dodecane and compound 5, respectively, whereas with commercial piperonyl butoxide the mortality was 68%. The latter compound, which is known as a synergist insecticide, was as inhibitory to the symbiotic fungus as the synthetic compound 5. The possibility of controlling these insects in the future using compounds that can target simultaneously both organisms is discussed. © 2001 Society of Chemical Industry.en
dc.format.extent603-608-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAntifungal activityen
dc.subjectAtta sexdensen
dc.subjectLeaf-cutting anten
dc.subjectLeucoagaricus gongylophorusen
dc.subjectPiperonyl compoundsen
dc.subject1 (3,4 methylenedioxybenzyloxy)octaneen
dc.subjectantifungal agenten
dc.subjectbenzyl alcohol derivativeen
dc.subjectbromideen
dc.subjectdecaneen
dc.subjectdodecaneen
dc.subjectiodideen
dc.subjectoctaneen
dc.subjectpesticideen
dc.subjectpipamperoneen
dc.subjectpiperonyl alcoholen
dc.subjectpiperonyl butoxideen
dc.subjectunclassified drugen
dc.subjectanten
dc.subjectfungusen
dc.subjectinsecticideen
dc.subjectsymbionten
dc.subjecttoxicityen
dc.subjectanimalen
dc.subjectantifungal activityen
dc.subjectatta sexdensen
dc.subjectbioassayen
dc.subjectchemistryen
dc.subjectdrug effecten
dc.subjectfungus growthen
dc.subjectmetabolismen
dc.subjectmortalityen
dc.subjectnonhumanen
dc.subjectplant leafen
dc.subjectsymbiosisen
dc.subjectAnimalsen
dc.subjectAntifungal Agentsen
dc.subjectAntsen
dc.subjectBenzyl Alcoholsen
dc.subjectBiological Assayen
dc.subjectBromidesen
dc.subjectFungien
dc.subjectIodidesen
dc.subjectPesticide Synergistsen
dc.subjectPiperonyl Butoxideen
dc.subjectPlant Leavesen
dc.subjectSymbiosisen
dc.subjectFormicidaeen
dc.subjectHexapodaen
dc.titleToxicity of synthetic piperonyl compounds to leaf-cutting ants and their symbiotic fungusen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)-
dc.description.affiliationCentro de Estudos de Insetos Sociais Universidade Estadual Paulista UNESP, Caixa Postal 199, CEP 13506-900, Rio Claro - SP-
dc.description.affiliationDepartamento de Química Univ. Federal de São Carlos, Caixa Postal 676, CEP 13565-905, São Carlos - SP-
dc.description.affiliationUnespCentro de Estudos de Insetos Sociais Universidade Estadual Paulista UNESP, Caixa Postal 199, CEP 13506-900, Rio Claro - SP-
dc.identifier.doi10.1002/ps.333-
dc.identifier.wosWOS:000169672900004-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofPest Management Science-
dc.identifier.scopus2-s2.0-0034934664-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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