A method for high-efficiency cutting and rapid propagation of blue flower dan
A technology of blue flower dan and cuttings, applied in horticultural methods, botanical equipment and methods, plant regeneration, etc., can solve the problems of unfavorable cost, easy to cause pollution, control, etc., achieve simple and easy operation, reduce pollution, reduce cost effect
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Embodiment 1
[0030] Embodiment 1 cutting propagation in advance
[0031] (1) Aseptic sowing and germination
[0032] Aseptic sowing of seeds: Harvest mature blueflower fruits from October to December and dry them in a constant temperature hair dryer at 40°C. After they are completely dried and most of the seeds burst, they should be manually rubbed properly to make the seeds completely crack. Collect and record the number of seeds, put them into kraft paper bags and mark them, and store them in a dark and dry seed bank for later use. Select mature, plump and pest-free blue flower seeds, soak the seeds in tap water at 28°C for 0-2 days, soak them in washing powder water for 0.5 hours, and then rinse them with running water for 2 hours. 2 Soak for single-factor complete random disinfection treatment, and then inoculate on the medium described in Tables 2 and 3 for two-factor and three-level aseptic germination treatment, inoculate 3 seeds in each bottle, and repeat 3 times for each treatmen...
Embodiment 2
[0051] After the cutting propagation in advance of embodiment 1, treat that the rooted scion grows to more than 10cm, can cut the scion for the second time, and the length is no more than 1 / 2 of the original length. Insert the newly cut shoots as the second-generation scion (abbreviated as F2) into MS medium containing NAA (0.51.01.5mg / L), IBA (0.51.01.5mg / L), and hormone-free . The result is as follows:
[0052] Table 5 Screening table of inducing hormones for rooting of aseptic cuttings of Lanhuadan F2
[0053]
[0054] It can be seen from Table 5 that the rooting condition of the second-generation scion of Lanhuadan in the hormone blank medium has reached or exceeded that of the medium using IBA. Compared with the blank medium and IBA medium, the medium containing NAA could not effectively induce the rooting of F2 scions, and a large number of calluses would appear.
[0055] Will contain 1.0mg·L -1 NAA, 0.5mg·L -1 From the plants obtained on IBA and blank medium, th...
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