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dc.contributor.authorvan Doorn W.G.
dc.contributor.authorÇelikel F.G.
dc.contributor.authorPak C.
dc.contributor.authorHarkema H.
dc.date.accessioned2020-06-21T09:42:10Z
dc.date.available2020-06-21T09:42:10Z
dc.date.issued2013
dc.identifier.issn0031-9317
dc.identifier.urihttps://doi.org/10.1111/j.1399-3054.2012.01690.x
dc.identifier.urihttps://hdl.handle.net/20.500.12712/4980
dc.descriptionPubMed: 22974423en_US
dc.description.abstractIt is not known whether tepal senescence in Iris flowers is regulated by hormones. We applied hormones and hormone inhibitors to cut flowers and isolated tepals of Iris × hollandica cv. Blue Magic. Treatments with ethylene or ethylene antagonists indicated lack of ethylene involvement. Auxins or auxin inhibitors also did not change the time to senescence. Abscisic acid (ABA) hastened senescence, but an inhibitor of ABA synthesis (norflurazon) had no effect. Gibberellic acid (GA3) slightly delayed senescence in some experiments, but in other experiments it was without effect, and gibberellin inhibitors [ancymidol or 4-hydroxy-5-isopropyl-2-methylphenyltrimethyl ammonium chloride-1-piperidine carboxylate (AMO-1618)] were ineffective as well. Salicylic acid (SA) also had no effect. Ethylene, auxins, GA3 and SA affected flower opening, therefore did reach the flower cells. Jasmonates delayed senescence by about 2.0 days. Similarly, cytokinins delayed senescence by about 1.5-2.0 days. Antagonists of the phosphatidylinositol signal transduction pathway (lithium), calcium channels (niguldipine and verapamil), calmodulin action [fluphenazine, trifluoroperazine, phenoxybenzamide and N-(6-aminohexyl)-5-chloro-1-naphtalenesulfonamide hydrochloride (W-7)] or protein kinase activity [1-(5-isoquinolinesulfonyl)-2-methylpiperazine hydrochloride (H-7), N-[2-(methylamino)ethyl]-5-isoquinolinesulfonamide hydrochloride (H-8) and N-(2-aminoethyl)-5-isoquinolinesulfonamide dihydrochloride (H-9)] had no effect on senescence, indicating no role of a few common signal transduction pathways relating to hormone effects on senescence. The results indicate that tepal senescence in Iris cv. Blue Magic is not regulated by endogenous ethylene, auxin, gibberellins or SA. A role of ABA can at present not be excluded. The data suggest the hypothesis that cytokinins and jasmonates are among the natural regulators. © Physiologia Plantarum 2012.en_US
dc.language.isoengen_US
dc.relation.isversionof10.1111/j.1399-3054.2012.01690.xen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleDelay of Iris flower senescence by cytokinins and jasmonatesen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume148en_US
dc.identifier.issue1en_US
dc.identifier.startpage105en_US
dc.identifier.endpage120en_US
dc.relation.journalPhysiologia Plantarumen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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