Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/34524
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dc.contributor.authorLavanya, A R-
dc.contributor.authorMuthukumar, M-
dc.contributor.authorMuthukrishnan, S-
dc.contributor.authorKumaresan, V-
dc.contributor.authorKumar, T Senthil-
dc.contributor.authorRao, A S-
dc.contributor.authorRao, M V-
dc.date.accessioned2016-06-28T03:50:20Z-
dc.date.available2016-06-28T03:50:20Z-
dc.date.issued2016-01-
dc.identifier.issn0975-0967 (Online); 0972-5849 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/34524-
dc.description107-111en_US
dc.description.abstractAn efficient and improved micropropagation protocol was developed from different explants of 2-month-old seedlings of Simarouba glauca DC. The highest number of shoots (55.3) with 100% response was obtained from cotyledonary-node explant on MS medium fortified with 6-benzyl adenine (BA; 3.0 mg/L), kinetin (KN; 0.5 mg/L), α-naphthalene acetic acid (NAA; 0.5 mg/L) and glutamine (10 mg/L). Further, the highest rooting response (95%) with 15 roots of 5.8 cm root length was observed on MS medium supplemented with NAA (3.0 mg/L). The rooted plantlets were hardened by transferring to paper containers with soil and sand (2:1) and kept in shade for acclimatization. These plants were further transferred to the field with a survival percentage of 81.5%.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJBT Vol.15(1) [January 2016]en_US
dc.subjectAdditivesen_US
dc.subjectGrowth regulatorsen_US
dc.subjectMicropropagationen_US
dc.subjectSimarouba glaucaen_US
dc.subjectShoot multiplicationen_US
dc.titleIn vitro micropropagation of Simarouba glauca DC.en_US
dc.typeArticleen_US
Appears in Collections:IJBT Vol.15(1) [January 2016]

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