2006
DOI: 10.17660/actahortic.2006.725.37
|View full text |Cite
|
Sign up to set email alerts
|

Healthy in Vitro Propagation by Meristem Tip Culture of Helleborus Niger¿s Selected Clone for Cut Flower

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
2

Citation Types

0
10
0

Year Published

2012
2012
2021
2021

Publication Types

Select...
3
1
1

Relationship

0
5

Authors

Journals

citations
Cited by 6 publications
(10 citation statements)
references
References 0 publications
0
10
0
Order By: Relevance
“…The axillary buds of four hellebore species (H. argutifolius, H. foetidus, H. niger, H. orientalis) were also used successfully for in vitro initiation on modified MS medium enriched with 2iP and BAP [17] or on MS medium supplemented with BAP, 2iP and NAA [19]. Poupet et al [11] produced virus-indexed H. niger plants only from the apical meristem on medium containing: kinetin, GA 3 , and IBA. Apical buds of H. niger seedlings were isolated and established on medium supplemented with BAP and GA 3 [16].…”
Section: Discussionmentioning
confidence: 99%
See 3 more Smart Citations
“…The axillary buds of four hellebore species (H. argutifolius, H. foetidus, H. niger, H. orientalis) were also used successfully for in vitro initiation on modified MS medium enriched with 2iP and BAP [17] or on MS medium supplemented with BAP, 2iP and NAA [19]. Poupet et al [11] produced virus-indexed H. niger plants only from the apical meristem on medium containing: kinetin, GA 3 , and IBA. Apical buds of H. niger seedlings were isolated and established on medium supplemented with BAP and GA 3 [16].…”
Section: Discussionmentioning
confidence: 99%
“…Apical buds of H. niger seedlings were isolated and established on medium supplemented with BAP and GA 3 [16]. [11,16,17]. The multiplication rate was significantly higher for H. niger than for H. argutifolius, H. foetidus, and H. orientalis [17].…”
Section: Discussionmentioning
confidence: 99%
See 2 more Smart Citations
“…In a nursery environment, the chilling of young plants stimulated growth (Lowder et al, 2010) and accelerated flowering time (Christiaens et al, 2012). As it turned out, microshoot multiplication and rooting in vitro is more effective at a temperature of around 15 o C (Seyring, 2002;Poupet et al, 2006;Dhooghe and van Labeke, 2007;Beruto and Curir, 2009;Gabryszewska, 2014). Establishing of this condition can be a problem due to the cost of cooling.…”
Section: Introductionmentioning
confidence: 99%