Tissue culture and rapid propagation method of hippophae rhamnoides
A technology for tissue culture rapid propagation and sea buckthorn, which is applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems of low survival rate, easy spread of diseases, low reproduction coefficient of root and tiller, etc., so as to improve the rooting rate. Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0071] The invention provides a tissue culture rapid propagation method of seabuckthorn, comprising the following steps:
[0072] (1) Inoculate the sterilized Seabuckthorn stem section with dormant buds into the starting medium for cultivation, the cultivation conditions are: light intensity: 1200lx, photoperiod: 11h / d, temperature: 26°C;
[0073] (2) Inoculate the vigorously growing stem segments into the rooting medium for cultivation, the cultivation conditions are: light intensity: 1900lx, photoperiod: 16h / d, temperature: 26°C.
[0074] in,
[0075] The formula of the starting medium is: 1 / 3MS+30g / L of sucrose+7g / L of agar+0.3mg / L of IBA.
[0076] The formula of described rooting medium is:
[0077] KNO 3 : 950mg / L;
[0078] NH 4 NO 3 : 825mg / L;
[0079] K H 2 PO 4 : 85mg / L;
[0080] MgSO 4 ·7H 2 O: 185mg / L;
[0081] CaCl 2 2H 2 O: 220mg / L;
[0082] KI: 0.415mg / L;
[0083] h 3 BO 3 : 3.1mg / L;
[0084] MnSO 4 4H 2 O: 11.15mg / L;
[0085] ZnSO 4 ·7H 2...
Embodiment 2
[0102] The invention provides a tissue culture rapid propagation method of seabuckthorn, comprising the following steps:
[0103] (1) Inoculate the sterilized seabuckthorn stem section with dormant buds into the starting medium for cultivation, the cultivation conditions are: light intensity: 1100lx, photoperiod: 12h / d, temperature: 27°C;
[0104] (2) Inoculate the vigorously growing stem segments into the rooting medium for cultivation, the cultivation conditions are: light intensity: 1800 lx, photoperiod: 16h / d, temperature: 27°C.
[0105] in,
[0106] The formula of the starting medium is: 1 / 3MS+30g / L of sucrose+7g / L of agar+0.4mg / L of IBA.
[0107] The formula of described rooting medium is:
[0108] KNO 3 : 950mg / L;
[0109] NH 4 NO 3 : 825mg / L;
[0110] K H 2 PO 4 : 85mg / L;
[0111] MgSO 4 ·7H 2 O: 185mg / L;
[0112] CaCl 2 2H 2 O: 220mg / L;
[0113] KI: 0.415mg / L;
[0114] h 3 BO 3 : 3.1mg / L;
[0115] MnSO 4 4H 2 O: 11.15mg / L;
[0116] ZnSO 4 ·7H ...
Embodiment 3
[0133] The invention provides a tissue culture rapid propagation method of seabuckthorn, comprising the following steps:
[0134] (1) Inoculate the sterilized Seabuckthorn stem section with dormant buds into the starting medium for cultivation, the cultivation conditions are: light intensity: 1300lx, photoperiod: 10h / d, temperature: 25°C;
[0135] (2) Inoculate the vigorously growing stem segments into the rooting medium for cultivation, the cultivation conditions are: light intensity: 2000lx, photoperiod: 16h / d, temperature: 25°C.
[0136] in,
[0137] The formulation of the starting medium is: 1 / 3MS + 30 g / L sucrose + 7 g / L agar + 0.2 mg / L IBA.
[0138] The formula of described rooting medium is:
[0139] KNO 3 : 950mg / L;
[0140] NH 4 NO 3 : 825mg / L;
[0141] K H 2 PO 4 : 85mg / L;
[0142] MgSO 4 ·7H 2 O: 185mg / L;
[0143] CaCl 2 2H 2 O: 220mg / L;
[0144] KI: 0.415mg / L;
[0145] h 3 BO 3 : 3.1mg / L;
[0146] MnSO 4 4H 2 O: 11.15mg / L;
[0147] ZnSO 4 ·7...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More