Method for inducing blueberries to root by using liquid culturing media and permeable matrix
A liquid culture medium and permeability technology, applied in horticultural methods, botanical equipment and methods, applications, etc., can solve the problems of difficulty in rooting bilberry in vitro, low transplant survival rate, long period of rooting, etc. The effects of rapid propagation on an industrial scale, high transplant survival rate, and strong permeability
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Embodiment 1
[0032] Embodiment 1: prepare the filter paper group of 0.8cmx1.2cm size, join 1 / 2WPM+IBA1.0mg.L -1 + Edible white sugar 2% + pH 5.0 rooting induction nutrient solution, soak the filter paper balls into the rooting induction culture liquid and put them into bottles, add 6 to 10 filter paper balls to each bottle, then inject 3 ~ 5ml of the rooting induction culture liquid, cover After that, at 1.2Kg / cm 2 , Sterilize under saturated steam pressure at 121°C for 20 minutes. On the ultra-clean workbench, transfer the robust rootless bilberry seedlings of 40 days of subculture and 3 to 4 cm in height to the rooting medium for cultivation. Under intermittent light conditions, the light intensity is 1500-2000 lx, and the daily light is 12 hours. A root system with 3-7 roots and a root length of 0.5-2 cm can be formed in 30 days. Take out the rooted test-tube plantlets from the culture bottle, transplant them directly to the seedbed with peat soil and moss volume ratio = 1:1, pour 1 / 2...
Embodiment 2
[0033] Embodiment 2: prepare the absorbent cotton ball of 0.8cmx1.2cm size, mix 1 / 2WPM+IBA5.0mg.L -1 +Edible white sugar 2%+pH 5.2 induction rooting nutrient solution, soak the absorbent cotton balls in the induction rooting culture solution and put them into bottles, 6-10 per bottle, then inject 3-5ml of the induction rooting culture solution, after sealing with polypropylene film, At 1.2Kg / cm 2 , Sterilize under saturated steam pressure at 121°C for 20 minutes. On the ultra-clean workbench, divide the robust rootless seedlings subcultured for 40 days with a height of 3 to 4 cm, and transfer them to the rooting medium. Under the conditions of 12h / d intermittent light and light intensity of 1500-2000lx, adventitious roots can be induced for about 10 days, and after 10 days of culture, 3-7 root systems with a root length of 0.5-2cm can be formed. Take out the rooted test-tube plantlets from the culture bottle, transplant them directly to the seedbed with peat soil and moss vo...
Embodiment 3
[0034] Embodiment 3: choose the granular vermiculite of 0.2cmx0.6cm size, wash clean and tap water, put running water and rinse after 20~30min, dry in oven or dry naturally; prepare 1 / 2WPM+IBA1.0mg .L -1 + Edible white sugar 2% + pH 5.2 rooting induction nutrient solution; soak the vermiculite grains in the induction rooting culture solution and put them into bottles, 20-30 grains per bottle, then inject 3-5ml of the rooting induction culture solution, seal with polypropylene film , at 1.2Kg / cm 2 , Sterilize under saturated steam pressure at 121°C for 20 minutes. On the ultra-clean workbench, divide the robust rootless seedlings that have been subcultured for 40 days and have a height of 3-4 cm, and transfer them to the rooting medium. First, cultivate them in the dark for 7-10 days, and then transfer them to 12 h / d intermittent light. Adventitious roots can be induced in about 10 days, and the temperature of the culture room is 24±2°C. Cultivate the test-tube seedlings on ...
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