CN105010109A - Method for water planting grosvenor momordica - Google Patents
Method for water planting grosvenor momordica Download PDFInfo
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- CN105010109A CN105010109A CN201510385367.4A CN201510385367A CN105010109A CN 105010109 A CN105010109 A CN 105010109A CN 201510385367 A CN201510385367 A CN 201510385367A CN 105010109 A CN105010109 A CN 105010109A
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- momordica grosvenori
- root
- nutrient solution
- seedling
- cultivating groove
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01G—HORTICULTURE; CULTIVATION OF VEGETABLES, FLOWERS, RICE, FRUIT, VINES, HOPS OR SEAWEED; FORESTRY; WATERING
- A01G31/00—Soilless cultivation, e.g. hydroponics
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01H—NEW PLANTS OR NON-TRANSGENIC PROCESSES FOR OBTAINING THEM; PLANT REPRODUCTION BY TISSUE CULTURE TECHNIQUES
- A01H4/00—Plant reproduction by tissue culture techniques ; Tissue culture techniques therefor
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- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05B—PHOSPHATIC FERTILISERS
- C05B7/00—Fertilisers based essentially on alkali or ammonium orthophosphates
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- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05G—MIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
- C05G5/00—Fertilisers characterised by their form
- C05G5/20—Liquid fertilisers
- C05G5/23—Solutions
Abstract
The invention discloses provides a method for water planting grosvenor momordica. The method includes the steps of transplanting and water planting management. A disinfected basal part of a grosvenor momordica rooted seedling is wrapped with sponge, and transplanted to a cultivation groove with water planting nutrient solution, so that 1/2-5/6 of the root of the grosvenor momordica rooted seedling is immersed in the water planting nutrient solution. After the grosvenor momordica rooted seedling is transplanted, the pH value of the water planting nutrient solution is maintained between 5.5-6.5, and air is breathed in a pipe body each day for 30 minutes. When no more than 1/3 of the root is immersed in the water planting nutrient solution, the water planting nutrient solution is replaced. In the method, the water planting nutrient solution meets the requirement for plant growth. The water planted grosvenor momordica has well developed root systems, strong stalks, and dense green leaves. The water planted grosvenor momordica when transplanted to a field can resume growing vigor rapidly and meets the production requirements.
Description
Technical field
The present invention relates to a kind of cultivation method of Momordica grosvenori, more particularly, the present invention relates to a kind of ciltivating process of Momordica grosvenori.
Background technology
Momordica grosvenori is the perennial liane that Curcurbitaceae Momordica grosvenori belongs to, it is the distinctive medicinal and sweetener plant of China, be not only the herbal species that pharmacopeia is recorded, the Ye Shi Ministry of Public Health, State Administration of Traditional Chinese Medicine first list in and be food and the Chinese medicine of medicine register, be the famous genunie medicinal materials in Guangxi.The sapling multiplication of current Momordica grosvenori is mainly based on tissue cultures, therefore the transplant survival of plantlet in vitro is most important, conventional plantlet in vitro is transplanted main to be transplanted to booth nutrition cup, but liquid manure is used and bad control, premature application easily burns seedling, after using late, be difficult to meet growth requirement, growth retardation.The invention reside in and a kind of Luohanguo With Plantlets of Tissue Culture water culture technology is provided, supply feedwater, fertilizer, gas, temperature, light by the physiological period of plant completely, make Luohanguo With Plantlets of Tissue Culture well-grown, to improve plantlet in vitro transplanting survival rate and the growth rate of Momordica grosvenori.What lean on due to water planting is artificial climate simultaneously, not by the impact of Natural Water, temperature, light, can produce in the anniversary, has broken the restriction in season, improve the production efficiency of Momordica grosvenori seedling greatly.
Summary of the invention
An object of the present invention is to solve at least the problems referred to above and/or defect, and the advantage will illustrated at least is below provided.
A further object of the invention is to provide a kind of ciltivating process of Momordica grosvenori, by the coated sponge of base portion of seedling of taking root at Momordica grosvenori, base portion can be protected by the article scratch of outside, and making Momordica grosvenori take root seedling more can Adaptable growth environment.
A further object of the invention is 1/2 ~ 5/6 the immersing in described mill water culture nutrient solution of root system of seedling of being taken root by Momordica grosvenori, makes mill water culture nutrient solution can not exceed the pseudobulb of Momordica grosvenori root, reserves a part of root and contacts with air and breathe.
In order to realize, according to these objects of the present invention and other advantage, providing a kind of ciltivating process of Momordica grosvenori, comprise the following steps:
Transplant: the base portion of seedling of being taken root by the Momordica grosvenori after sterilization is coated with sponge, is transplanted into afterwards and contains in the cultivating groove of mill water culture nutrient solution, make Momordica grosvenori take root seedling root system 1/2 ~ 5/6 immerse in described mill water culture nutrient solution;
Wherein, described cultivating groove is provided with lid supporting with it, described lid is provided with the second through hole that first through hole and several aperture are the seedling of taking root with fixing described Momordica grosvenori of 2 ~ 4cm, be inserted with body in described first through hole, the outlet side of described body and described Momordica grosvenori take root the root of seedling in same level;
Water planting manages: described Momordica grosvenori is taken root after transplantation of seedlings, the pH value of described mill water culture nutrient solution is kept to be between 5.5 ~ 6.5, every day passes into air 30min in described body, when the root system of Momordica grosvenori is no more than 1/3 described in mill water culture nutrient solution submergence, then changes described mill water culture nutrient solution.
Preferably, described Momordica grosvenori take root the breeding method of seedling be will cultivate through subculture and the leaf look dark green aseptic tissue culture plant inoculation of Momordica grosvenori in root media, cultivate to taking root, the sucrose of the methyl α-naphthyl acetate containing MS, 0.2mg/L in described root media, the indolebutyric acid of 0.1mg/L, the agar of 4.5g/L and 30g/L.
Preferably, the described mill water culture nutrient solution of every 10L contains following component: calcium nitrate tetrahydrate 810 ~ 830mg, potassium nitrate 580 ~ 620mg, ammonium dihydrogen phosphate (ADP) 140 ~ 160mg, magnesium sulfate 365 ~ 375mg, disodium ethylene diamine tetraacetate iron 13 ~ 19mg, four hydrated manganese sulfate 0.6 ~ 0.8mg, boric acid 1.0 ~ 1.4mg, Salzburg vitriol 0.02 ~ 0.06mg, zinc sulphate 0.06 ~ 0.1mg and molybdic acid 0.01mg.
Preferably, 10th ~ 15 days after transplanting, described mill water culture nutrient solution is replaced to beer waste water nutrient solution, and wherein, it is 1000: 1 ~ 5: 10 ~ 15 to form in mass ratio that described beer waste water nutrient solution is less than or equal to the beer waste water of 120mg/L, acidifying bacterium and trace element by COD value.
Preferably, described cultivating groove is glass material, the take root cultivating groove of seedling of Momordica grosvenori is had to be placed in Momordica grosvenori culturing device by transplanting, and magnetic stir bar is added in cultivating groove, wherein, described Momordica grosvenori culturing device comprises the magnetic stirring apparatus of light-passing board and the described cultivating groove of carrying, described light-passing board and magnetic stirring apparatus are fixed by several support column, described light-passing board is provided with LED light source, after Momordica grosvenori takes root transplantation of seedlings, every day magnetic stir bar and magnetic stirring apparatus to the mill water culture nutrient solution in described cultivating groove for or beer waste water nutrient solution stir 2-3 hour.
Preferably, the Momordica grosvenori after transplanting is taken root, and seedling maintains the temperature at 22 ~ 25 DEG C, intensity of illumination is 8200 ~ 8500Lx.
Preferably, the salpeter solution or the mass fraction that regulate the reagent of pH to be mass fraction to be 5% are the sodium hydroxide solution of 5%.
Preferably, Momordica grosvenori of sterilizing take root the method for seedling be Momordica grosvenori is taken root seedling put into mass fraction be 0.1% carbendazim solution soak 10 ~ 20 minutes.
The present invention at least comprises following beneficial effect:
1, adopt the Momordica grosvenori of water planting of the present invention, its mill water culture nutrient solution can meet plant strain growth demand, and through the Momordica grosvenori that water planting is cultivated, well developed root system, cane is sturdy, and leaf look dark green, and restoration ecosystem gesture that can be very fast when transferring to field planting, meets Production requirement.
2, by the coated sponge of base portion of seedling of taking root at Momordica grosvenori, base portion can be protected by the article scratch of outside, making Momordica grosvenori take root seedling more can Adaptable growth environment.
3, a kind of special cultivating groove is set, by arranging the first through hole, eliminates and Momordica grosvenori is taken root the fixing of seedling, this device can be utilized to carry out large-area water planting to Momordica grosvenori, convenient management.
4, pass into air to the take root root of seedling of the close Momordica grosvenori of cultivating groove, prevent the root anaerobic respiration of Momordica grosvenori too much, thus generate alcohol and cause rotten.
5, Momordica grosvenori to be taken root 1/2 ~ 5/6 the immersing in described mill water culture nutrient solution of root system of seedling, make mill water culture nutrient solution can not exceed the pseudobulb of Momordica grosvenori root, reserve a part of root and contact with air and breathe.
6, when Momordica grosvenori takes root the 10-15 days of seedling water planting, adopt beer waste water Solution culture method Momordica grosvenori to take root seedling, namely make use of discarded beer waste water, the material simultaneously in beer waste water can promote the growth rate of Momordica grosvenori, shortens the cultivation time of Momordica grosvenori.
7, by Momordica grosvenori culturing device, liquid in cultivating groove can be stirred, the root of Momordica grosvenori can not be injured, also make inner liquid mixing evenly, root absorption is more abundant, adopts LED light source to arrange intensity of illumination for 8200-8500Lx and can meet needed for the growth of Momordica grosvenori.
Part is embodied by explanation below by other advantage of the present invention, target and feature, part also will by research and practice of the present invention by those skilled in the art is understood.
Accompanying drawing explanation
Fig. 1 the present invention is provided with the structure chart of the cultivating groove of lid;
Fig. 2 is the structure chart of Momordica grosvenori culturing device of the present invention.
Embodiment
Below in conjunction with embodiment, the present invention is described in further detail, can implement according to this with reference to specification word to make those skilled in the art.
Embodiment 1
As Figure 1-Figure 2, a kind of ciltivating process of Momordica grosvenori, comprises the following steps:
Transplant: the base portion of seedling of being taken root by the Momordica grosvenori after sterilization is coated with sponge, is transplanted into afterwards and contains in the cultivating groove 2 of mill water culture nutrient solution, make Momordica grosvenori take root seedling root system 1/2 immerse in described mill water culture nutrient solution;
Wherein, described cultivating groove 2 is provided with lid 1 supporting with it, described lid 1 is provided with the second through hole that first through hole and several aperture are the seedling of taking root with fixing described Momordica grosvenori of 2cm, be inserted with body in described first through hole, the outlet side of described body and described Momordica grosvenori take root the root of seedling in same level;
Water planting manages: described Momordica grosvenori is taken root after transplantation of seedlings, and keep the pH value of described mill water culture nutrient solution to be 5.5, every day passes into air 30min in described body, when the root system of Momordica grosvenori is no more than 1/3 described in mill water culture nutrient solution submergence, then changes described mill water culture nutrient solution.
Wherein, described Momordica grosvenori take root the breeding method of seedling be will cultivate through subculture and the leaf look dark green aseptic tissue culture plant inoculation of Momordica grosvenori in root media, cultivate to taking root, the sucrose of the methyl α-naphthyl acetate containing MS, 0.2mg/L in described root media, the indolebutyric acid of 0.1mg/L, the agar of 4.5g/L and 30g/L.
Wherein, the described mill water culture nutrient solution of every 10L contains following component: calcium nitrate tetrahydrate 810mg, potassium nitrate 580mg, ammonium dihydrogen phosphate (ADP) 140mg, magnesium sulfate 365mg, disodium ethylene diamine tetraacetate iron 13mg, four hydrated manganese sulfate 0.6mg, boric acid 1.0mg, Salzburg vitriol 0.02mg, zinc sulphate 0.06mg and molybdic acid 0.01mg.
Wherein, the 10th day after transplanting, described mill water culture nutrient solution is replaced to beer waste water nutrient solution, and wherein, it is to form at 1000: 1: 10 in mass ratio that described beer waste water nutrient solution is less than or equal to the beer waste water of 120mg/L, acidifying bacterium and trace element by COD value.
Wherein, described cultivating groove 2 is glass material, the take root cultivating groove 2 of seedling of Momordica grosvenori is had to be placed in Momordica grosvenori culturing device by transplanting, and magnetic stir bar is added in cultivating groove 2, wherein, described Momordica grosvenori culturing device comprises the magnetic stirring apparatus 3 of light-passing board 4 and the described cultivating groove 2 of carrying, described light-passing board 4 and magnetic stirring apparatus 3 are fixed by several support column 6, described light-passing board 4 is provided with LED light source 5, after Momordica grosvenori takes root transplantation of seedlings, every day magnetic stir bar and magnetic stirring apparatus 3 to the mill water culture nutrient solution in described cultivating groove 2 for or beer waste water nutrient solution stir 2 hours.
Wherein, the Momordica grosvenori after transplanting is taken root, and seedling maintains the temperature at 22 DEG C, intensity of illumination is 8200Lx.
Wherein, the salpeter solution or the mass fraction that regulate the reagent of pH to be mass fraction to be 5% are the sodium hydroxide solution of 5%.
Wherein, Momordica grosvenori of sterilizing take root the method for seedling be Momordica grosvenori is taken root seedling put into mass fraction be 0.1% carbendazim solution soak 10 minutes.
Embodiment 2
As Figure 1-Figure 2, a kind of ciltivating process of Momordica grosvenori, comprises the following steps:
Transplant: the base portion of seedling of being taken root by the Momordica grosvenori after sterilization is coated with sponge, is transplanted into afterwards and contains in the cultivating groove 2 of mill water culture nutrient solution, make Momordica grosvenori take root seedling root system 5/6 immerse in described mill water culture nutrient solution;
Wherein, described cultivating groove 2 is provided with lid 1 supporting with it, described lid 1 is provided with the second through hole that first through hole and several aperture are the seedling of taking root with fixing described Momordica grosvenori of 4cm, be inserted with body in described first through hole, the outlet side of described body and described Momordica grosvenori take root the root of seedling in same level;
Water planting manages: described Momordica grosvenori is taken root after transplantation of seedlings, and keep the pH value of described mill water culture nutrient solution to be 6.5, every day passes into air 30min in described body, when the root system of Momordica grosvenori is no more than 1/3 described in mill water culture nutrient solution submergence, then changes described mill water culture nutrient solution.
Wherein, described Momordica grosvenori take root the breeding method of seedling be will cultivate through subculture and the leaf look dark green aseptic tissue culture plant inoculation of Momordica grosvenori in root media, cultivate to taking root, the sucrose of the methyl α-naphthyl acetate containing MS, 0.2mg/L in described root media, the indolebutyric acid of 0.1mg/L, the agar of 4.5g/L and 30g/L.
Wherein, the described mill water culture nutrient solution of every 10L contains following component: calcium nitrate tetrahydrate 830mg, potassium nitrate 620mg, ammonium dihydrogen phosphate (ADP) 160mg, magnesium sulfate 375mg, disodium ethylene diamine tetraacetate iron 19mg, four hydrated manganese sulfate 0.8mg, boric acid 1.4mg, Salzburg vitriol 0.06mg, zinc sulphate 0.1mg and molybdic acid 0.01mg.
Wherein, the 15th day after transplanting, described mill water culture nutrient solution is replaced to beer waste water nutrient solution, and wherein, it is to form at 1000: 5: 15 in mass ratio that described beer waste water nutrient solution is less than or equal to the beer waste water of 120mg/L, acidifying bacterium and trace element by COD value.
Wherein, described cultivating groove 2 is glass material, the take root cultivating groove 2 of seedling of Momordica grosvenori is had to be placed in Momordica grosvenori culturing device by transplanting, and magnetic stir bar is added in cultivating groove 2, wherein, described Momordica grosvenori culturing device comprises the magnetic stirring apparatus 3 of light-passing board 4 and the described cultivating groove 2 of carrying, described light-passing board 4 and magnetic stirring apparatus 3 are fixed by several support column 6, described light-passing board 4 is provided with LED light source 5, after Momordica grosvenori takes root transplantation of seedlings, every day magnetic stir bar and magnetic stirring apparatus 3 to the mill water culture nutrient solution in described cultivating groove 2 for or beer waste water nutrient solution stir 3 hours.
Wherein, the Momordica grosvenori after transplanting is taken root, and seedling maintains the temperature at 25 DEG C, intensity of illumination is 8500Lx.
Wherein, the salpeter solution or the mass fraction that regulate the reagent of pH to be mass fraction to be 5% are the sodium hydroxide solution of 5%.
Wherein, Momordica grosvenori of sterilizing take root the method for seedling be Momordica grosvenori is taken root seedling put into mass fraction be 0.1% carbendazim solution soak 20 minutes.
Embodiment 3
As Figure 1-Figure 2, a kind of ciltivating process of Momordica grosvenori, comprises the following steps:
Transplant: the base portion of seedling of being taken root by the Momordica grosvenori after sterilization is coated with sponge, is transplanted into afterwards and contains in the cultivating groove 2 of mill water culture nutrient solution, make Momordica grosvenori take root seedling root system 1/3 immerse in described mill water culture nutrient solution;
Wherein, described cultivating groove 2 is provided with lid 1 supporting with it, described lid 1 is provided with the second through hole that first through hole and several aperture are the seedling of taking root with fixing described Momordica grosvenori of 3cm, be inserted with body in described first through hole, the outlet side of described body and described Momordica grosvenori take root the root of seedling in same level;
Water planting manages: described Momordica grosvenori is taken root after transplantation of seedlings, and keep the pH value of described mill water culture nutrient solution to be 6, every day passes into air 30min in described body, when the root system of Momordica grosvenori is no more than 1/3 described in mill water culture nutrient solution submergence, then changes described mill water culture nutrient solution.
Wherein, described Momordica grosvenori take root the breeding method of seedling be will cultivate through subculture and the leaf look dark green aseptic tissue culture plant inoculation of Momordica grosvenori in root media, cultivate to taking root, the sucrose of the methyl α-naphthyl acetate containing MS, 0.2mg/L in described root media, the indolebutyric acid of 0.1mg/L, the agar of 4.5g/L and 30g/L.
Wherein, the described mill water culture nutrient solution of every 10L contains following component: calcium nitrate tetrahydrate 820mg, potassium nitrate 600mg, ammonium dihydrogen phosphate (ADP) 150mg, magnesium sulfate 370mg, disodium ethylene diamine tetraacetate iron 16mg, four hydrated manganese sulfate 0.7mg, boric acid 1.2mg, Salzburg vitriol 0.04mg, zinc sulphate 0.08mg and molybdic acid 0.01mg.
Wherein, the 12nd day after transplanting, described mill water culture nutrient solution is replaced to beer waste water nutrient solution, and wherein, it is to form at 1000: 3: 12 in mass ratio that described beer waste water nutrient solution is less than or equal to the beer waste water of 120mg/L, acidifying bacterium and trace element by COD value.
Wherein, described cultivating groove 2 is glass material, the take root cultivating groove 2 of seedling of Momordica grosvenori is had to be placed in Momordica grosvenori culturing device by transplanting, and magnetic stir bar is added in cultivating groove 2, wherein, described Momordica grosvenori culturing device comprises the magnetic stirring apparatus 3 of light-passing board 4 and the described cultivating groove 2 of carrying, described light-passing board 4 and magnetic stirring apparatus 3 are fixed by several support column 6, described light-passing board 4 is provided with LED light source 5, after Momordica grosvenori takes root transplantation of seedlings, every day magnetic stir bar and magnetic stirring apparatus 3 to the mill water culture nutrient solution in described cultivating groove 2 for or beer waste water nutrient solution stir 2.5 hours.
Wherein, the Momordica grosvenori after transplanting is taken root, and seedling maintains the temperature at 23 DEG C, intensity of illumination is 8300Lx.
Wherein, the salpeter solution or the mass fraction that regulate the reagent of pH to be mass fraction to be 5% are the sodium hydroxide solution of 5%.
Wherein, Momordica grosvenori of sterilizing take root the method for seedling be Momordica grosvenori is taken root seedling put into mass fraction be 0.1% carbendazim solution soak 15 minutes.
Although embodiment of the present invention are open as above, but it is not restricted to listed in specification and embodiment utilization, it can be applied to various applicable the field of the invention completely, for those skilled in the art, can easily realize other amendment, therefore do not deviating under the universal that claim and equivalency range limit, the present invention is not limited to specific details and illustrates here and the legend described.
Claims (8)
1. a ciltivating process for Momordica grosvenori, is characterized in that, comprises the following steps:
Transplant: the base portion of seedling of being taken root by the Momordica grosvenori after sterilization is coated with sponge, is transplanted into afterwards and contains in the cultivating groove of mill water culture nutrient solution, make Momordica grosvenori take root seedling root system 1/2 ~ 5/6 immerse in described mill water culture nutrient solution;
Wherein, described cultivating groove is provided with lid supporting with it, described lid is provided with the second through hole that first through hole and several aperture are the seedling of taking root with fixing described Momordica grosvenori of 2 ~ 4cm, be inserted with body in described first through hole, the outlet side of described body and described Momordica grosvenori take root the root of seedling in same level;
Water planting manages: described Momordica grosvenori is taken root after transplantation of seedlings, the pH value of described mill water culture nutrient solution is kept to be between 5.5 ~ 6.5, every day passes into air 30min in described body, when the root system of Momordica grosvenori is no more than 1/3 described in mill water culture nutrient solution submergence, then changes described mill water culture nutrient solution.
2. the ciltivating process of Momordica grosvenori as claimed in claim 1, it is characterized in that, described Momordica grosvenori take root the breeding method of seedling be will cultivate through subculture and the leaf look dark green aseptic tissue culture plant inoculation of Momordica grosvenori in root media, cultivate to taking root, the sucrose of the methyl α-naphthyl acetate containing MS, 0.2mg/L in described root media, the indolebutyric acid of 0.1mg/L, the agar of 4.5g/L and 30g/L.
3. the ciltivating process of Momordica grosvenori as claimed in claim 2, it is characterized in that, the described mill water culture nutrient solution of every 10L contains following component: calcium nitrate tetrahydrate 810 ~ 830mg, potassium nitrate 580 ~ 620mg, ammonium dihydrogen phosphate (ADP) 140 ~ 160mg, magnesium sulfate 365 ~ 375mg, disodium ethylene diamine tetraacetate iron 13 ~ 19mg, four hydrated manganese sulfate 0.6 ~ 0.8mg, boric acid 1.0 ~ 1.4mg, Salzburg vitriol 0.02 ~ 0.06mg, zinc sulphate 0.06 ~ 0.1mg and molybdic acid 0.01mg.
4. the ciltivating process of Momordica grosvenori as claimed in claim 3, it is characterized in that, 10th ~ 15 days after transplanting, described mill water culture nutrient solution is replaced to beer waste water nutrient solution, wherein, described beer waste water nutrient solution is less than or equal to the beer waste water of 120mg/L, acidifying bacterium and trace element by COD value is 1000: 1 ~ 5: 10 ~ 15 to form in mass ratio.
5. the ciltivating process of Momordica grosvenori as claimed in claim 4, it is characterized in that, described cultivating groove is glass material, the take root cultivating groove of seedling of Momordica grosvenori is had to be placed in Momordica grosvenori culturing device by transplanting, and magnetic stir bar is added in cultivating groove, wherein, described Momordica grosvenori culturing device comprises the magnetic stirring apparatus of light-passing board and the described cultivating groove of carrying, described light-passing board and magnetic stirring apparatus are fixed by several support column, described light-passing board is provided with LED light source, after Momordica grosvenori takes root transplantation of seedlings, every day magnetic stir bar and magnetic stirring apparatus to the mill water culture nutrient solution in described cultivating groove for or beer waste water nutrient solution stir 2-3 hour.
6. the ciltivating process of Momordica grosvenori as claimed in claim 5, is characterized in that, the Momordica grosvenori after transplanting is taken root, and seedling maintains the temperature at 22 ~ 25 DEG C, intensity of illumination is 8200 ~ 8500Lx.
7. the ciltivating process of Momordica grosvenori as claimed in claim 6, is characterized in that, the salpeter solution or the mass fraction that regulate the reagent of pH to be mass fraction to be 5% are the sodium hydroxide solution of 5%.
8. the ciltivating process of Momordica grosvenori as claimed in claim 7, is characterized in that, sterilization Momordica grosvenori take root the method for seedling be Momordica grosvenori is taken root seedling put into mass fraction be 0.1% carbendazim solution soak 10 ~ 20 minutes.
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