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

Inactive Publication Date: 2010-05-05
LUDONG UNIVERSITY
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  • Abstract
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  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Bilberry has been improved, cultivated and planted in the United States and Canada for nearly a hundred years. my country began to introduce excellent varieties of bilberry from the United States and Canada in the 1990s, and carried out research on rapid propagation of seedlings, but the expansion and promotion of conventional breeding methods is slow. , the research on rapid propagation of tissue culture in vitro, most authors report: Vaccinium test tube rooting difficulties, low rooting rate, long rooting cycle, low transplanting survival rate (Rowland et al., 1992; Dweikate et al., 1998; Wang Xiali, etc. , 2003; Liu Shuying et al., 2004; Tao Jianmin et al., 2006), restricting the industrialized seedling raising process of good varieties, therefore, it is very important to select a kind of efficient and fast induced rooting method for the rapid propagation and popularization of bilberry

Method used

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Examples

Experimental program
Comparison scheme
Effect test

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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Abstract

The invention discloses a method for inducing blueberries to root by using liquid culture media and permeable matrix, comprising the following steps: (1) preparing rooting culturing media; (2) transferring the healthy and strong blueberry seedlings which are subcultured for 40d and are 3-4 cm high into the rooting culturing media, culturing the blueberry seedlings for 7-10d in the dark and for 12h/d for about 20d under intermitted illumination condition until the blueberry seedlings have 3-7 root systems of 0.5-2 cm long; and (3) transplanting the test-tube blueberry seedlings which are cultured for 30d to root, are 3-6 cm high and have the root length of 0.5-2 cm into the media in which the proportion of turfy soil to moss is 1:1, and managing the blueberry seedlings. The rooting culturing media is prepared according to the following substeps: 1) preparing 0.8 cm*1.2 cm filtering paper balls or defatted cotton balls or 0.2 cm*0.6 cm vermiculites which function as the matrix of the rooting culturing media; 2) preparing rooting culturing solution which has the WPM of 1/2, the IBA of 1.0-5.0 mg.L-1, the edible white sugar of 2 percent and the pH value of 5.0-5.2; and 3) adding 6-10 filtering paper balls or defatted cotton balls or 20-30 vermiculites which are soaked by the rooting culturing solution and adding 3-5 ml rooting culturing solution to each culturing bottle and capping the culturing to sterilize according to the routine method. The invention has short rooting period and low production cost, can ensure that 100 percent of the blueberry seedlings can root and over 95 percent of the transplanted blueberry seedlings can survive and realize the rapid industrialized propagation of the blueberry seedlings on a large scale.

Description

technical field [0001] The invention belongs to the technical field of plant tissue culture rapid propagation, in particular to a method for inducing rooting of bilberry test tubes by means of a liquid medium attached with a permeable matrix. Background technique [0002] Bilberry has another name called blueberry and blue berry, and it is a small berry fruit tree of the genus Vaccinium in the Rhododendronaceae (Ericaceae). Bilberry fruit has delicate pulp, very small seeds, sweet and sour taste, and refreshing and pleasant aroma. The unique bilberry anthocyanins, arbutin, SOD and other substances in the fruit have the effects of improving eyesight, anti-aging, eliminating fatigue and preventing cancer. Both Japan and the United States list bilberry in the forefront of anti-cancer foods, known as "21st Century Functional Health Berries" and "Queen of Fruits". Bilberry is not only a good product for fresh food, but also can be further processed into high value-added product...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A01H4/00
Inventor 赵建萍蒋小满张萍柏新富
Owner LUDONG UNIVERSITY
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