Use este identificador para citar ou linkar para este item: http://www.alice.cnptia.embrapa.br/alice/handle/doc/313294
Registro completo de metadados
Campo DCValorIdioma
dc.contributor.authorSCHOTTZ, E. de S.pt_BR
dc.contributor.authorKALIL FILHO, A. N.pt_BR
dc.contributor.authorTRACZ, A. L.pt_BR
dc.contributor.authorKOEHLER, H.pt_BR
dc.contributor.authorRIBAS, L. L. F.pt_BR
dc.contributor.authorQUOIRIN, M.pt_BR
dc.date.accessioned2011-04-10T11:11:11Zpt_BR
dc.date.available2011-04-10T11:11:11Zpt_BR
dc.date.created2007-08-06pt_BR
dc.date.issued2007pt_BR
dc.identifier.citationCiência Florestal, Santa Maria, v. 17, n. 1/2, p. 109-117, jan./mar. 2007.pt_BR
dc.identifier.urihttp://www.alice.cnptia.embrapa.br/alice/handle/doc/313294pt_BR
dc.descriptionBig-leaf mahogany (Swietenia macrophylla King) is an important species for timber production that is considered the most valuable in the world. For this reason its exploitation is indiscriminate and leads this species to the risk of extinction. Moreover, mahogany is difficult to regenerate naturally and, when used in reforestation programs, plants are severely damaged by the shoot-borer (Hypsipyla grandella Zellar). This work aimed at developing the multiplication stage of micropropagation of Swietenia macrophylla King using juvenile material. After desinfestation, seeds were germinated in MS solid culture medium. Shoot formation from seeds occurred during five months, giving 5.54 nodal segments per seed. These explants were excised, each containing one axillary bud, and transferred on multiplication media. Four experiments with cytokinins were conducted, using media supplemented with 6-benzylaminopurine (BAP) (2.5 to 50.0 ?M), 2- isopentenyladenine (2-iP) (0; 1.1 to 8.8 ?M), combinations of BAP (0; 2.5 to 50.0 ?M) and 2-iP (2.2 ?M). For the first treatments the basal culture medium was MS medium and in the last one MS and QL media were used in separate experiments. When BAP was tested alone, the maximum point of multiplication rate average was obtained on medium containing 23.61 ?M, while 2-iP did not induce bud multiplication. On QL culture medium supplemented with the combinations of BAP (0; 2.5; 5.0; 10.0 e 20.0 ?M ) and 2-iP (2.2 ?M), there was no multiplication. The maximum point of multiplication rate average was 5.7 ?M, obtained when the MS culture medium was supplemented with 18.51 ?M BAP and 2.2 ?M 2-iP.pt_BR
dc.language.isoengeng
dc.rightsopenAccesseng
dc.subjectMahoganypt_BR
dc.subjectTropical speciespt_BR
dc.titleIn vitro multiplication of Swietenia macrophylla King (Meliaceae) from juvenile shoots.pt_BR
dc.typeArtigo de periódicopt_BR
dc.date.updated2015-02-13T11:11:11Zpt_BR
dc.subject.nalthesauruscytokininspt_BR
dc.subject.nalthesaurusmicropropagationpt_BR
riaa.ainfo.id313294pt_BR
riaa.ainfo.lastupdate2015-02-13pt_BR
dc.contributor.institutionEliane de souza Schottz, UFPR; Antonio Nascim Kalil Filho, Embrapa Florestas; Anderson Luiz Tracz, UFPR; Henrique Koehler, UFPR; Luciana L. F. Ribas, UFPR; Marguerite Quoirin, UFPR.pt_BR
Aparece nas coleções:Artigo em periódico indexado (CNPF)

Arquivos associados a este item:
Arquivo Descrição TamanhoFormato 
MULTIPLICACAOINVITRODESwieteniamacrophyllaKINGMELIACEAEAPARTIRDE.pdf286,42 kBAdobe PDFThumbnail
Visualizar/Abrir
Mostrar registro simples do item Visualizar estatísticas

FacebookTwitterDeliciousLinkedInGoogle BookmarksMySpace