1996
DOI: 10.1016/0304-4238(96)00874-6
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Adventitious shoot formation from carnation stem segments: a comparison of different culture procedures

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Cited by 23 publications
(9 citation statements)
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“…In the liquid medium, while the percentage of shoot-forming carnation petals met expectations, the number of regenerated shoots from those petals was lower than expected. Although the vessels were shaken, this observation may be due to anoxia, with similar results occurring in carnation stems (Watad et al 1996). On the other hand, differences in the regenerative capacity of White Sim petals between the first (8.5 shoots per petal) and the second experiment (2.8 shoots per petal), both performed in 8 g dm -3 agar, can be attributed to seasonal variations in the organogenic potential of tissues, which is higher in spring than in winter.…”
Section: Discussionsupporting
confidence: 72%
“…In the liquid medium, while the percentage of shoot-forming carnation petals met expectations, the number of regenerated shoots from those petals was lower than expected. Although the vessels were shaken, this observation may be due to anoxia, with similar results occurring in carnation stems (Watad et al 1996). On the other hand, differences in the regenerative capacity of White Sim petals between the first (8.5 shoots per petal) and the second experiment (2.8 shoots per petal), both performed in 8 g dm -3 agar, can be attributed to seasonal variations in the organogenic potential of tissues, which is higher in spring than in winter.…”
Section: Discussionsupporting
confidence: 72%
“…MV, in which microshoots were permanently submerged in the liquid medium without forced air supply and lack of mechanical stress, was characterized with the lowest growth parameters, probably due to asphyxia which outweighed the benefits of better tissue-medium contact (as compared to agar culture) (Watad et al 1996).…”
Section: Bioreactor Systemsmentioning
confidence: 99%
“…To facilitate the continued genetic improvement of Dianthus, a range of in vitro tissue culture techniques have been developed. For example, efficient systems have been established for the regeneration of plants from leaf explants and stem segments (Jethwani and Kothari 1996;Watad et al 1996;Kantia and Kothari 2002) and for the induction of direct somatic embryogenesis from leaf and petal cells (Nakano and Mii 1993;Yantcheva et al 1998;Pareek and Kothari 2003;Karami et al 2006). Although anther culture has been carried out for inducing somatic embryogenesis in various plant species (Achar 2002;Germanà 2003;Kikkert et al 2005;Rimberia et al 2005), there have been a few reports on anther culture of Dianthus species (DolcetSanjuan et al 2001).…”
Section: Introductionmentioning
confidence: 97%