Inoculation method for shortening rapid propagation growth cycle of phalaenopsis
A growth cycle, Phalaenopsis technology, applied in the field of inoculation to shorten the rapid propagation growth cycle of Phalaenopsis, can solve the problems of increased production cost, increased production capacity, bud variation, etc.
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Embodiment 1
[0030] The strong buds are cut and inoculated, and the strong buds meet the following conditions: the leaves are dark green, the stems and leaves in the lateral buds are differentiated, and the stems are thick;
[0031] Cut along the junction of the topmost blade and stem of the strong buds, remove the terminal buds from the strong buds, and insert 1 strong bud into the culture medium for 21 days. The insertion depth in the medium was all 0.20 of the bud height. The culture conditions are: the light is 1800lux, the average temperature is 25°C, the light is 12 hours a day, and the light time is from 7:00 to 19:00; the components and contents of the medium are as follows: the weight ratio is 100:10:4:0.2:1.5 MS medium, mashed potatoes, mashed bananas, ascorbic acid and corn juice.
[0032] See the results of the training figure 1 .
Embodiment 2
[0034] Weak buds are cut and inoculated, and the weak buds meet the following conditions: the leaves are light green or white buds, and the stems and leaves in the lateral buds are undifferentiated;
[0035] Keep the terminal buds of the weak buds, separate the weak buds with a straight knife along the bud gap, and insert 2 weak buds into the medium for cultivation for 21 days. The insertion depth of the weak buds in the medium is equal to that of bud 0.20 of the body height. The culture conditions are: the light is 1800lux, the temperature is 25°C, the light is 12 hours a day, and the light time is 7:00-19:00; the components and contents of the medium are as follows: MS with a weight ratio of 100:10:4:0.2:1.5 Culture medium, mashed potatoes, mashed bananas, ascorbic acid and corn juice.
[0036] See the results of the training figure 2 .
Embodiment 3
[0038] According to the method of Example 1, the difference is that the insertion depth of the strong buds in the culture medium is 0.15 of the height of the bud body.
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