Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/5846
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dc.contributor.authorTamta, Sushma-
dc.contributor.authorPalni, L M S-
dc.date.accessioned2009-08-10T08:12:02Z-
dc.date.available2009-08-10T08:12:02Z-
dc.date.issued2004-04-
dc.identifier.issn0975-0967 (Online); 0972-5849 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/5846-
dc.description209-215en_US
dc.description.abstractAdventitious bud formation was examined in zygotic embryos (decoated seeds) of Cedrus deodara, planted in the normal position, using four different media variously supplemented with or without plant growth regulators (PGRs). Following incubation for 7, 14, 21 and 28 days on PGR containing media, the embryos were transferred to respective PGR-free basal media. While embryo swelling was observed in all cases, normal germination was observed only in embryos cultured initially in PGR-free media. Best response, in terms of bud formation (93%), was observed in embryos first cultured on LP medium containing BA and Kinetin (1.0 M each) for 28 days and then transferred to LP medium without any PGR. While the mean number of shoots formed per cultured embryo was also highest (34%) in this combination, these shoots eventually dried when excised and sub-cultured for further multiplication. Success was, however, obtained when the embryos were initially planted in an inverted position on LP medium containing 20.0 M BA for 10 days, and then shifted, again in the inverted position, on the same medium without BA. Although the mean number of shoots formed was low (only 2.5 shoots per embryo), these could be multiplied and elongated. The microshoots (2.0-3.0 cm) thus obtained could be rooted (100%) using ½ strength, PGR-free, LP medium, hardened and established in pots. Besides excised embryos, stem segments were also used as explants. While only a quarter of explants could be established in culture, in contamination-free condition, good sprouting response (3-4 buds per segment) was obtained in certain PGR combinations. The sprouted buds developed into shoots on LP medium containing 5.0 M BA; further subculturing of excised shoots for multiplication, however, resulted in drying up of shoots. Further work is required to overcome this difficulty.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt Cl.7 A 01 H 4/00, 7/00en_US
dc.sourceIJBT Vol.3(2) [April 2004]en_US
dc.subjectCedrus deodaraen_US
dc.subjectconiferen_US
dc.subjectdeodaren_US
dc.subjectmicropropagationen_US
dc.subjectinverted embryo techniqueen_US
dc.subjectstem segmentsen_US
dc.subjectrootingen_US
dc.titleStudies on in vitro propagation of Himalayan cedar (Cedrus deodara) using zygotic embryos and stem segmentsen_US
dc.typeArticleen_US
Appears in Collections:IJBT Vol.03(2) [April 2004]

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