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dc.contributor.authorKenny, Lahcen, 1958-
dc.creatorKenny, Lahcen, 1958-en_US
dc.date.accessioned2013-03-28T10:19:26Z
dc.date.available2013-03-28T10:19:26Z
dc.date.issued1988en_US
dc.identifier.urihttp://hdl.handle.net/10150/276843
dc.description.abstractIn vitro organogenesis of jojoba has been attempted using a variety of explants, and highly concentrated nutrient media similar to Murashige and Skoog medium. This study found that, unlike many other woody plant species, jojoba tissue is very sensitive to high concentration of mineral salts. Modified versions of Woody plant medium, and Lyrene medium were very successful for growth and proliferation of shoot apices. A multiplication rate of 50 shoots per original explant in 3 months was achieved in the presence of high concentration of Ca (22 meg/L), and an auxin cytokinin ratio of 20 (2 mg/L of BAP, and 0.1 mg/L of NAA). An average of 5 roots/shoot were obtained when the base of the shoots were wounded prior to treatment with 100 ppm IBA solution for 5 sec, and then subsequently cultured on a MS medium containing 10 mg/L IBA, and 0.1 mg/L NAA. (Abstract shortened with permission of author.)
dc.language.isoen_USen_US
dc.publisherThe University of Arizona.en_US
dc.rightsCopyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.en_US
dc.subjectJojoba -- Micropropagation.en_US
dc.titleDevelopment of an in vitro micropropagation system for jojoba (Simmondsia chinensis (Link) Schneider)en_US
dc.typetexten_US
dc.typeThesis-Reproduction (electronic)en_US
dc.identifier.oclc21768057en_US
thesis.degree.grantorUniversity of Arizonaen_US
thesis.degree.levelmastersen_US
dc.identifier.proquest1335406en_US
thesis.degree.disciplineGraduate Collegeen_US
thesis.degree.disciplinePlant Sciencesen_US
thesis.degree.nameM.S.en_US
dc.identifier.bibrecord.b17309062en_US
refterms.dateFOA2018-09-04T02:56:14Z
html.description.abstractIn vitro organogenesis of jojoba has been attempted using a variety of explants, and highly concentrated nutrient media similar to Murashige and Skoog medium. This study found that, unlike many other woody plant species, jojoba tissue is very sensitive to high concentration of mineral salts. Modified versions of Woody plant medium, and Lyrene medium were very successful for growth and proliferation of shoot apices. A multiplication rate of 50 shoots per original explant in 3 months was achieved in the presence of high concentration of Ca (22 meg/L), and an auxin cytokinin ratio of 20 (2 mg/L of BAP, and 0.1 mg/L of NAA). An average of 5 roots/shoot were obtained when the base of the shoots were wounded prior to treatment with 100 ppm IBA solution for 5 sec, and then subsequently cultured on a MS medium containing 10 mg/L IBA, and 0.1 mg/L NAA. (Abstract shortened with permission of author.)


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