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dc.contributor.authorOzdemir, F.A. and Yildirim, M.U. and Kahriz, M.P. and Kilic, O.
dc.date.accessioned2021-04-08T12:08:53Z
dc.date.available2021-04-08T12:08:53Z
dc.date.issued2016
dc.identifier.issn13119109
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84962694311&partnerID=40&md5=33558c2d2acb2be5155e6e7d72ce2e91
dc.identifier.urihttp://acikerisim.bingol.edu.tr/handle/20.500.12898/4708
dc.description.abstractAttractive blue-flowering Scilla siberica subsp. armena bulbs multiply very slowly in 4-5 years under natural conditions. Therefore, this study aimed to accelerate multiplication by devising a strategy for an efficient in vitro bulblet regeneration system using peduncle and bulb scale explants on MS medium containing 0.25, 0.50, 1.00, and 2.00 mg l-1 TDZ, plus 0.10 or 0.20 mg l-1 2,4-D (8 combinations). Bulb scale explants weredifficult to culture due to high fungal infection and were, therefore, discarded. The peduncle explants induced direct bulblet regeneration after swelling on explants. Maximum mean number of bulblets and bulb diameter was acheived on MS medium containing 1.00 mg l-1 TDZ + 0.20 mg l-1 2,4-D. The regenerated bulblets were isolated from peduncle explants and cultured on MS medium containing 40 g l-1 sucrose, where they grew in diameter and rooted.
dc.language.isoEnglish
dc.sourcePropagation of Ornamental Plants
dc.titleIn Vitro bulblet regeneration from Scilla Siberica haw. subsp. armena (grosh.) mordak peduncle


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