Tissue culture rapid propagation method of Japanese maple orange dream
A technology for tissue culture rapid propagation and maple orange, which is applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems of large-scale production and development and application of orange dream, the germination rate and survival rate are not high, and cannot be satisfied. Seedling needs and other issues, to achieve the effects of fast reproduction, large growth, and good economic benefits
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Embodiment 1
[0034] Embodiment 1—Acer palmatum orange dream seedling rooting control test
[0035] Taking the breeding of Acer palmatum orange dream seedlings as an example, the above-mentioned examples were tested respectively. After transplanting, the seedlings of Acer palmatum orange dream were all managed in the same way under the same conditions, and were treated with conventional water and fertilizer methods. Manage until out of the nursery. Measure the rooting days of the dream seedling of Acer palmatum orange in 60 days after transplanting, and the obtained data tabulation 1 is as follows:
[0036] Table 1—Experiment on the days of rooting of Acer palmatum orange dream seedlings
[0037] test subject
Embodiment 2
[0038] Embodiment 2—Control experiment on survival rate of dream seedlings of Acer palmatum orange
[0039] Taking the breeding of Acer palmatum orange dream seedlings as an example, the above-mentioned examples were tested respectively. After transplanting, the seedlings of Acer palmatum orange dream were all managed in the same way under the same conditions, and were treated with conventional water and fertilizer methods. Manage until out of the nursery. 60 days after transplanting, measure the survival rate of the dream seedlings of the acquired Acer palmatum orange, and the obtained data list 2 is as follows:
[0040] Table 2—Experiment on the survival rate of dream seedlings of Acer palmatum orange
[0041] test subject
specific Embodiment approach 1
[0043] Specific embodiment 1: the composition of described starting medium is: 1 / 2WPM basic medium, supplement 0.2mg / LIAA, 0.04mg / LIBA, 0.1mg / LNAA, 0.04mg / LGA3, 20g / L sucrose, 4g / L agar.
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