Micropropagation protocol of Oriental Hybrid
Lilium
cv. Ravenna was developed using bulb scale segments (Basal and Tip) as explants. Surface sterilization of healthy bulb scales with carbendazim 200 ppm for 30 min, then 0.1 percent mercuric chloride for 10 min, then 70% ethyl alcohol for 30 s was superior to all other treatments in recording highest culture asepsis (77.08%) and higher explant survival (86.12%). Explant survival was higher in basal segments (88.54%) compared to tip segments (85.52%). Highest culture establishment was recorded in basal scale segments (68.26%) followed by tip scale segments (55.21%). MS medium augmented with 0.50 mgl
−1
Naphthalene acetic acid and 2.0 mgl
−1
. 6-Benzylamino Purine recorded maximum culture establishment (76.17%), highest bulblet number/explant (5.52) with maximum length of shoots (2.20 cm) and number of leaves (3.39). This treatment combination of growth regulators resulted in highest shoot proliferation (83.33%) along with maximum shoot number (2.41explant
−1
), shoot length (2.35 cm) and leaf number (5.44) of micro shoots during proliferation stage. Rooting of explants was superior with Indole-3-butyric acid compared to Naphthalene acetic acid. Highest rooting of 92.71% along with maximum number of primary roots shoot
−1
(12.06), maximum primary root length (3.17 cm) was documented in Murashige and Skoog medium added with Indole-3-butyric acid 1.50 mgl
−1
with best
ex vitro
survival rate (98.96%) of rooted plantlets during primary hardening in perlite + vermiculite (1:1) mixture.
Chrysanthemum (Dendranthemum grandiflorum kitam.) is a leading flower with applied value worldwide. Flower color is an important trait that influences the commercial value of chrysanthemum cultivars. Developing new chrysanthemum cultivars with novel characteristics such as new flower colors in a time-and cost-efficient manner is the ultimate goal for breeders. Understanding the molecular mechanisms that regulate flower pigmentation may provide important implications for the rationale manipulation of flower color. To generate diverse array of flower colour mutants in chrysanthemum cv. "Candid" through mutagenesis, in vitro grown micro shoots were exposed to 10, 20, 30 and 40 Gy gamma irradiation at 100 Gy per minute and were evaluated for different parameters. The rhizogenesis parameters decreased with the increase in irradiation dose from 0 Gy to 40 Gy, while as, 10 Gy dose proved to record minimum decline as compared to the control. Survival, leaf size and number of leaves plant −1 after 8th week interval also decreased with the increasing trend of gamma irradiation dose but recorded minimum decline in plants developed from shoots irradiated with 10 Gy gamma irradiation dose with respect to the control. Apparently minimum delay in number of days to floral bud appearance took under 10 Gy as compared to control. Highest number of flower colour mutants were recorded under 10 Gy (light pink, orange pink,white and yellow). Amountable mutation frequency on the basis of flower colour was desirable in plants irradiated with least dose of 10 Gy.
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