Efficient rooting method for rhododendron lapponicum tissue culture seedlings
A technique for tissue culture seedlings and rhododendrons, applied in the field of efficient rooting of alpine rhododendron tissue culture seedlings, can solve the problems of high vitrification rate, difficult rooting, easy browning of explants, etc., and achieve the effect of large number and increased survival rate
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Embodiment 1
[0023] Embodiment 1 pure sphagnum moss substrate planting technology and existing containing a small amount of sphagnum moss substrate planting technology
[0024] 1. Experimental steps
[0025] 1) Materials and treatment: Select healthy and pollution-free Rhododendron alpine tissue culture cluster buds (such as figure 1 ), on the ultra-clean workbench, cut about 3-5cm with a scalpel, and the sprouts of 4-5 leaves are inoculated into the buffered rooting medium, the buffered medium is: WPM basic medium, add NAA:IBA= 0.25mg / L: 0.25mg / L, soft white sugar 30g / L, activated carbon 1g / L, agar powder 6g / L. After cultivating in dark for 7 days;
[0026] 2) Place the tissue culture bottle in an intelligent greenhouse at a temperature of 25°C-28°C, cover it with white non-woven fabric, harden the seedlings for 3 days, take out the sprouts, soak them in 800 times carbendazim disinfectant for 15 minutes, and place them on a newspaper Set aside after drying;
[0027] 3) Pure sphagnum m...
Embodiment 2
[0034] 1. Materials: Healthy and pollution-free alpine rhododendron tissue culture cluster buds
[0035] 2. Method
[0036] (1) Treatment method of clustered buds of Rhododendron alpine: Use a scalpel to cut about 3-5cm and 4-5 leaf buds on the ultra-clean bench, inoculate them into the buffered rooting basic medium: WPM basic medium, add soft white sugar 30g / L, gac 1g / L, agar powder 6g / L), add 4 kinds (g1, g2, g3, g4) in the buffer rooting medium of different hormone ratios simultaneously, wherein (g1=(NAA:IBA=1.5 :0.5), g2=(NAA:IBA=1.0:0.5), g3=(NAA:IBA=0.5:0.5), g4=(NAA:IBA=0.25:0.25)), put 8 cluster buds in every bottle, Five bottles of each medium were inoculated, repeated three times, and then the treatment was placed in the tissue culture room, under dark conditions, for 7 days, and the culture temperature was 25-28°C.
[0037] (2) After 7 days, place the tissue culture bottle in an intelligent greenhouse at a temperature of 25°C-30°C, cover it with a white non-woven ...
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