CN107473790A - A kind of rare earth culture medium for golden mushroom and implantation methods - Google Patents

A kind of rare earth culture medium for golden mushroom and implantation methods Download PDF

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Publication number
CN107473790A
CN107473790A CN201710645201.0A CN201710645201A CN107473790A CN 107473790 A CN107473790 A CN 107473790A CN 201710645201 A CN201710645201 A CN 201710645201A CN 107473790 A CN107473790 A CN 107473790A
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Prior art keywords
rare earth
parts
asparagus
culture medium
bottle
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CN201710645201.0A
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周仁杰
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Tianjin Mao Mushroom Development Co Ltd
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Tianjin Mao Mushroom Development Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C05FERTILISERS; MANUFACTURE THEREOF
    • C05CNITROGENOUS FERTILISERS
    • C05C5/00Fertilisers containing other nitrates

Abstract

The invention discloses a kind of rare earth culture medium for golden mushroom, its drip irrigation device is to include 20 24 parts of rice bran, 28 30 parts of corncob, 46 parts of corn flour, 46 parts of dregs of beans, 10 14 parts of wheat bran, 24 parts of megasse, 35 parts of cotton seed hulls, 1 part of calcium carbonate, 0.4 0.6 parts of micro element supplement agent, 0.1 0.15 parts of rare earth accelerator, the growth for promoting asparagus and the increase of protein content are reached, the further quality for improving asparagus, it has been finally reached the growth of synchronous promotion asparagus and the increase of protein content, improve the technique effect of the product competitiveness of manufacturing enterprise.

Description

A kind of rare earth culture medium for golden mushroom and implantation methods
Technical field
The present invention relates to golden mushroom plantation field, more particularly to a kind of rare earth culture medium for golden mushroom and implantation methods.
Background technology
Asparagus scientific name hair handle money bacterium, also known as hair handle small fire mushroom, structure bacterium, plain mushroom, dried mushroom, plain wild rice, jelly bacterium, golden mushroom, intelligence Power mushroom etc., English are:“Enoki Mushroom”.Because its stem is elongated, like day lily, therefore claims asparagus, belong to the white mushroom of Agaricales Section's pin gold mushroom category, is a kind of bacterium algae lichens.Asparagus has very high medicinal dietary function.
Asparagus is widely distributed in nature, and the ground such as China, Japan, Russia, Europe, North America, Australia has Distribution., from the east of Jiangsu, the growth of asparagus is suitable for west to Xinjiang to Yunnan North gets Heilungkiang, south in China.
Asparagus is free of chlorophyll, without photosynthesis, it is impossible to carbohydrate is manufactured, but completely can be in dark surrounds Middle growth, it is necessary to ready-made organic substance is absorbed from culture medium, such as the degradation product of carbohydrate, protein and fat, is Metatrophy type, it is a kind of heterotrophic organism, belongs to basidiomycetes.Asparagus is a kind of timber saprophytic bacteria, is easily grown in willow, elm, white On the withered trunk and stub of the broad leaf trees such as willow.
The plantation of asparagus can realize industrialization at present, but the specific processing maturation period of asparagus still have it is certain Difference, and how finally to influence the growth cycle and nutriment of asparagus by implantation methods adjustment and the selection of culture medium Content, increase the benefit of enterprise, the profitability of enterprise is the problem of many edible mushroom enterprises are inquired into always.
The content of the invention
It is an object of the invention to provide a kind of rare earth culture medium for golden mushroom and implantation methods, serve the life for promoting asparagus Long and protein content increase, the further quality for improving asparagus, the growth of synchronous promotion asparagus has been finally reached it With the increase of protein content, the product competitiveness of manufacturing enterprise is improved.
The present invention above-mentioned technical purpose technical scheme is that:A kind of rare earth asparagus culture Base, count in parts by weight, include rice bran 20-24 parts, corncob 28-30 parts, corn flour 4-6 parts, dregs of beans 4-6 parts, wheat bran 10-14 parts, megasse 2-4 parts, cotton seed hulls 3-5 parts, 1 part of calcium carbonate, micro element supplement agent 0.4-0.6 parts, rare earth accelerator 0.1-0.15 parts.
Pass through above-mentioned technical proposal, the cooperation of the micro element supplement agent added in asparagus and rare earth accelerator can be with Promote the growth of asparagus and the increase of protein content, the further quality for improving asparagus, be finally reached synchronous rush Enter the growth of asparagus and the increase of protein content, improve the product competitiveness of manufacturing enterprise.
Preferably, micro element supplement agent includes potassium chloride and zinc sulfate.
Pass through above-mentioned technical proposal, Zn-ef ficiency and potassium element are all the trace elements required for asparagus, pass through micro member The supplement of element can promote the further growth of asparagus, ensure the trace element needed in asparagus rich in a variety of human bodies.
Preferably, the weight ratio of the potassium chloride and zinc sulfate in micro element supplement agent is 1:3.
Pass through above-mentioned technical proposal, micro- balanced collocation can ensure the reasonable growth of asparagus, guarantee fund Various micro- equilibriums in pin mushroom.
Preferably, rare earth accelerator is nitric acid rare earth.
Pass through above-mentioned technical proposal, the rare earth in rare earth accelerator are the rare earth element of ionic state, the rare earth of this state Element can be with relatively good passive plant absorption, and certain nitrogen can also be provided in nitrate anion, improves the life of asparagus It is long.
Preferably, the rare earth element in nitric acid rare earth is LREE.
Pass through above-mentioned technical proposal, the Elements Atom quality in LREE is smaller, while to human body and environment Toxic side effect very little, be healthier rare earth element, be more suitable for being used as fertilizer.
Preferably, comprise the following steps:
S1:The configuration of culture medium
Step 1:Include rice bran, corncob, ground rice, dregs of beans, wheat bran, megasse, cotton seed hulls, carry out first dry-mixed;
Step 3:Continue to add calcium carbonate, micro element supplement agent, the progress wet mixing of rare earth accelerator after addition running water, expect water Than for 1: 1.4-1.6;
Step 4:Water content detection is carried out, water content should be 60%~65%;
Step 5:Vexed 1~2h of heap is carried out, allows compost fully to absorb water;
Step 6:Mechanical bottling is carried out, every bottle about fills wet feed 250g-300g, is punched in bottle some;
Step 7:Install and autoclaving is used after bag, autoclave temperature is at 123-126 DEG C, sterilization time 1h;
S2:Inoculation strain is inoculated with Needle mushroom strain in the blake bottle of high-temperature sterilization, is then capped bottle cap, inoculation temperature It is arranged to 17-19 DEG C;
S3:The bacteria bacteria phase is usually 25-30 days, and bacteria phase indoor humidity is controlled in 75-80%, indoor temperature 14.5- 15℃;
S4:Mycelium stimulation is cleared up the upper strata aging mycelia in flammulina velatipes culture bottle, adds liquid fertilizer formulations 1-2 parts;
S5:Golden mushroom plantation
Step 1 culture probationary period (1-3 days), 15-17 DEG C of indoor temperature, indoor humidity 100%;
Step 2 culture is come into being the phase (4-10 days), and indoor temperature is progressively down to 5-7 DEG C from 15-17 DEG C;
Step 3 suppresses the phase (11-19 days), 4 DEG C of indoor temperature, bag mushroom is carried out to the asparagus in bottle;
Step 4 fast growing period (19-30 days) indoor temperature rises to 7 DEG C from 4 DEG C.
Then Pass through above-mentioned technical proposal, planting process plant asparagus first by allocating culture medium on culture medium, Liquid fertilizer preparation is added to culture medium in planting process, after the first damp Growth of Flammulina Velutipes can increase the battalion of culture medium The content of element is supported, therefore plays a part of relatively good promotion growth in Growth of Flammulina Velutipes.
Preferably, addition liquid fertilizer formulations include potassium dihydrogen phosphate and urea.
Pass through above-mentioned technical proposal, the fertilizer of the liquid of addition more easily culture medium can absorb, while spray process In can more easily allow Growth of Flammulina Velutipes than state that is more uniform, allowing culture medium to be integrally consistent.
Preferably, include 50mg urea and 40mg potassium dihydrogen phosphates in every gram of liquid fertilizer preparation.
Pass through above-mentioned technical proposal, the reasonably combined of liquid fertilizer preparation can promote asparagus smoothly to grow, and ensure The smooth growth of asparagus, so as to improve the yield of asparagus and shorten the fruiting phase of asparagus.
Preferably, liquid fertilizer preparation is sprayed directly on the surface of culture medium for golden mushroom.
Pass through above-mentioned technical proposal, it will be easier to absorb on the surface for being sprayed onto culture medium, asparagus can be ensured Smooth growth.
In summary, the invention has the advantages that:
1st, micro- intake can increase content micro- in asparagus, make the nutriment of asparagus rich with family It is rich;
2nd, the intake of zinc ion is important intelligence development ion, and the addition of zinc ion can promote the growth of asparagus in itself, simultaneously In edible asparagus, it is better able to increase the brain development of children;
3rd, LREE is have chosen in the selection of rare earth element, light rare earth typically refers to lanthanum, cerium, praseodymium, neodymium, promethium, samarium and europium Seven kinds of rare earth elements, they have a relatively low atomic number and smaller quality, thus it is edible when can avoid heavy metal ion It is toxic.
Embodiment
The present invention is described in further detail below.
Embodiment 1:Include rice bran 24g, corncob 30g, corn flour 6g, dregs of beans 6g, wheat bran 14g, megasse 4g, cottonseed Shell 5g, calcium carbonate 1g, potassium chloride 0.15g and zinc sulfate 0.45g, nitric acid rare earth 0.15g.
Asparagus implantation methods are as follows:
S1:The configuration of culture medium
Step 1:Include rice bran, corncob, ground rice, dregs of beans, wheat bran, megasse, cotton seed hulls, carry out first dry-mixed;
Step 3:Continue to add calcium carbonate, micro element supplement agent, the progress wet mixing of rare earth accelerator after addition running water, expect water Than for 1: 1.6;
Step 4:Water content detection is carried out, water content should be 65%;
Step 5:Vexed heap 2h is carried out, allows compost fully to absorb water;
Step 6:Mechanical bottling is carried out, every bottle about fills wet feed 300g, is punched in bottle some;
Step 7:Install and autoclaving is used after bag, autoclave temperature is at 126 DEG C, sterilization time 1h;
S2:Inoculation strain is inoculated with Needle mushroom strain in the blake bottle of high-temperature sterilization, is then capped bottle cap, inoculation temperature It is arranged to 19 DEG C;
S3:The bacteria bacteria phase is usually 30 days, and for the control of bacteria phase indoor humidity 80%, indoor temperature is 15 DEG C; S4:Mycelium stimulation Upper strata aging mycelia in flammulina velatipes culture bottle is cleared up, the liquid fertilizer preparation of addition include 100mg urea and 80mg potassium dihydrogen phosphates, it is left as 1820mg deionized waters;
S5:Golden mushroom plantation
Step 1 culture probationary period (1-3 days), 17 DEG C of indoor temperature, indoor humidity 100%;
Step 2 culture is come into being the phase (4-10 days), and indoor temperature is progressively down to 7 DEG C from 17 DEG C;
Step 3 suppresses the phase (11-19 days), 4 DEG C of indoor temperature, bag mushroom is carried out to the asparagus in bottle;
Step 4 fast growing period (19-30 days) indoor temperature rises to 7 DEG C from 4 DEG C.
Embodiment 2:Include rice bran 20g, corncob 28g, corn flour 4g, dregs of beans 4g, wheat bran 10g, megasse 2g, cottonseed Shell 3g, calcium carbonate 1g, potassium chloride 0.1g and zinc sulfate 0.3g, nitric acid rare earth 0.1g.
Asparagus implantation methods are as follows:
S1:The configuration of culture medium
Step 1:Include rice bran, corncob, ground rice, dregs of beans, wheat bran, megasse, cotton seed hulls, carry out first dry-mixed;
Step 3:Continue to add calcium carbonate, micro element supplement agent, the progress wet mixing of rare earth accelerator after addition running water, expect water Than for 1: 1.4;
Step 4:Water content detection is carried out, water content should be 60%;
Step 5:Vexed heap 1h is carried out, allows compost fully to absorb water;
Step 6:Mechanical bottling is carried out, every bottle about fills wet feed 250g, is punched in bottle some;
Step 7:Install and autoclaving is used after bag, autoclave temperature is at 123 DEG C, sterilization time 1h;
S2:Inoculation strain is inoculated with Needle mushroom strain in the blake bottle of high-temperature sterilization, is then capped bottle cap, inoculation temperature It is arranged to 17 DEG C;
S3:The bacteria bacteria phase is usually 25 days, and for the control of bacteria phase indoor humidity 75%, indoor temperature is 14.5 DEG C; S4:Scratch Bacterium is cleared up the upper strata aging mycelia in flammulina velatipes culture bottle, and the liquid fertilizer preparation of addition includes 50mg urea With 40mg potassium dihydrogen phosphates, it is left as 910mg deionized waters;
S5:Golden mushroom plantation
Step 1 culture probationary period (1-3 days), 15 DEG C of indoor temperature, indoor humidity 100%;
Step 2 culture is come into being the phase (4-10 days), and indoor temperature is progressively down to 5 DEG C from 15 DEG C;
Step 3 suppresses the phase (11-19 days), 4 DEG C of indoor temperature, bag mushroom is carried out to the asparagus in bottle;
Step 4 fast growing period (19-30 days) indoor temperature rises to 7 DEG C from 4 DEG C.
Embodiment 3:Include rice bran 22g, corncob 29g, corn flour 5g, dregs of beans 5g, wheat bran 12g, megasse 3g, cottonseed Shell 4g, calcium carbonate 1g, potassium chloride 0.125g and zinc sulfate 0.375g, nitric acid rare earth 0.125g.
Asparagus implantation methods are as follows:
S1:The configuration of culture medium
Step 1:Include rice bran, corncob, ground rice, dregs of beans, wheat bran, megasse, cotton seed hulls, carry out first dry-mixed;
Step 3:Continue to add calcium carbonate, micro element supplement agent, the progress wet mixing of rare earth accelerator after addition running water, expect water Than for 1: 1.5;
Step 4:Water content detection is carried out, water content should be 62.5%;
Step 5:Vexed heap 1.5h is carried out, allows compost fully to absorb water;
Step 6:Mechanical bottling is carried out, every bottle about fills wet feed 275g, is punched in bottle some;
Step 7:Install and autoclaving is used after bag, autoclave temperature is at 124.5 DEG C, sterilization time 1h;
S2:Inoculation strain is inoculated with Needle mushroom strain in the blake bottle of high-temperature sterilization, is then capped bottle cap, inoculation temperature It is arranged to 18 DEG C;
S3:The bacteria bacteria phase is usually 28 days, and for the control of bacteria phase indoor humidity 77.5%, indoor temperature is 14.75 DEG C;
S4:Mycelium stimulation is cleared up the upper strata aging mycelia in flammulina velatipes culture bottle, and the liquid fertilizer preparation of addition includes 75mg urea and 60mg potassium dihydrogen phosphates, is left as 1365mg deionized waters;
S5:Golden mushroom plantation
Step 1 culture probationary period (1-3 days), 16 DEG C of indoor temperature, indoor humidity 100%;
Step 2 culture is come into being the phase (4-10 days), and indoor temperature is progressively down to 5-7 DEG C from 15-17 DEG C;
Step 3 suppresses the phase (11-19 days), 4 DEG C of indoor temperature, bag mushroom is carried out to the asparagus in bottle;
Step 4 fast growing period (19-30 days) indoor temperature rises to 7 DEG C from 4 DEG C.
Embodiment 4:Include rice bran 22g, corncob 29g, corn flour 5g, dregs of beans 5g, wheat bran 12g, megasse 3g, cottonseed Shell 4g, calcium carbonate 1g, potassium chloride 0.15g and zinc sulfate 0.45g, nitric acid rare earth 0.15g;Remaining is same as Example 3.
Embodiment 5:Include rice bran 22g, corncob 29g, corn flour 5g, dregs of beans 5g, wheat bran 12g, megasse 3g, cottonseed Shell 4g, calcium carbonate 1g, potassium chloride 0.1g and zinc sulfate 0.3g, nitric acid rare earth 0.1g;Remaining is same as Example 3.
Comparative example is tested
Contents of Amino Acids refers to GB/T 15673-2009《The measure of crude protein content in edible mushroom》In kjeldahl determination Method;
All packed culture mediums are cultivated 25d and detected again.
Fruiting body yield is 20 bags of average values weighed.
Comparative example 1:Include rice bran 22g, corncob 29g, corn flour 5g, dregs of beans 5g, wheat bran 12g, megasse 3g, cottonseed Shell 4g, calcium carbonate 1g, potassium chloride 0.125g and zinc sulfate 0.375g;Remaining is same as Example 3.
Comparative example 2:Include rice bran 22g, corncob 29g, corn flour 5g, dregs of beans 5g, wheat bran 12g, megasse 3g, cottonseed Shell 4g, calcium carbonate 1g, nitric acid rare earth 0.125g;Remaining is same as Example 3.
Comparative example 3:Include rice bran 22g, corncob 29g, corn flour 5g, dregs of beans 5g, wheat bran 12g, megasse 3g, cottonseed Shell 4g, calcium carbonate 1g, potassium chloride 0.125g, nitric acid rare earth 0.125g;Remaining is same as Example 3.
Comparative example 4:Include rice bran 22g, corncob 29g, corn flour 5g, dregs of beans 5g, wheat bran 12g, megasse 3g, cottonseed Shell 4g, calcium carbonate 1g, potassium chloride 0.125g and zinc sulfate 0.375g, nitric acid rare earth 0.125g, liquid is not added with planting process Fertilizer formulations.
By the comparison of comparative example and embodiment it can be found that the rare earth element of the ionic state in nitric acid rare earth is to asparagus Growth has good facilitation, while the protein content of asparagus can also be allowed to increase to a certain extent, while is planting The liquid fertilizer added in journey is also the essential step in asparagus plantation, adds the implantation methods of liquid fertilizer The speed of growth and protein content that asparagus can be made can have been lifted;Micro element supplement agent coordinates rare earth supplement simultaneously Agent can play good mating reaction, and when lacking any one material, what the speed of growth of asparagus can be by a relatively large margin returns Fall.
This specific embodiment is only explanation of the invention, and it is not limitation of the present invention, people in the art Member can make the modification of no creative contribution to the present embodiment as needed after this specification is read, but as long as at this All protected in the right of invention by Patent Law.

Claims (9)

1. a kind of rare earth culture medium for golden mushroom, is counted in parts by weight, it is characterised in that:Include rice bran 20-24 parts, corncob 28-30 parts, corn flour 4-6 parts, dregs of beans 4-6 parts, wheat bran 10-14 parts, megasse 2-4 parts, cotton seed hulls 3-5 parts, 1 part of calcium carbonate, Micro element supplement agent 0.4-0.6 parts, rare earth accelerator 0.1-0.15 parts.
A kind of 2. rare earth culture medium for golden mushroom according to claim 1, it is characterised in that:Micro element supplement agent includes Potassium chloride and zinc sulfate.
A kind of 3. rare earth culture medium for golden mushroom according to claim 2, it is characterised in that:Chlorine in micro element supplement agent The weight ratio for changing potassium and zinc sulfate is 1:3.
A kind of 4. rare earth culture medium for golden mushroom according to claim 1, it is characterised in that:Rare earth accelerator is that nitric acid is dilute Soil.
A kind of 5. rare earth culture medium for golden mushroom according to claim 4, it is characterised in that:Rare earth element in nitric acid rare earth For LREE.
A kind of 6. implantation methods of rare earth asparagus, it is characterised in that:Comprise the following steps:
S1:The configuration of culture medium
Step 1:Include rice bran, corncob, ground rice, dregs of beans, wheat bran, megasse, cotton seed hulls, carry out first dry-mixed;
Step 3:Continue to add calcium carbonate, micro element supplement agent, the progress wet mixing of rare earth accelerator after addition running water, expect water Than for 1: 1.4-1.6;
Step 4:Water content detection is carried out, water content should be 60%~65%;
Step 5:Vexed 1~2h of heap is carried out, allows compost fully to absorb water;
Step 6:Mechanical bottling is carried out, every bottle about fills wet feed 250g-300g, is punched in bottle some;
Step 7:Install and autoclaving is used after bag, autoclave temperature is at 123-126 DEG C, sterilization time 1h;
S2:Inoculation strain is inoculated with Needle mushroom strain in the blake bottle of high-temperature sterilization, is then capped bottle cap, inoculation temperature It is arranged to 17-19 DEG C;
S3:The bacteria bacteria phase is usually 25-30 days, and bacteria phase indoor humidity is controlled in 75-80%, indoor temperature 14.5-15 ℃;
S4:Mycelium stimulation is cleared up the upper strata aging mycelia in flammulina velatipes culture bottle, adds liquid fertilizer formulations 1-2 parts;
S5:Golden mushroom plantation
Step 1 culture probationary period(1-3 days), 15-17 DEG C of indoor temperature, indoor humidity 100%;
Step 2 culture is come into being the phase(4-10 days), indoor temperature is progressively down to 5-7 DEG C from 15-17 DEG C;
Step 3 suppresses the phase(11-19 days), 4 DEG C of indoor temperature, bag mushroom is carried out to the asparagus in bottle;
Step 4 fast growing period(19-30 days)Indoor temperature rises to 7 DEG C from 4 DEG C.
A kind of 7. implantation methods of rare earth asparagus according to claim 6, it is characterised in that:Add liquid fertilizer formulations Include potassium dihydrogen phosphate and urea.
A kind of 8. implantation methods of rare earth asparagus according to claim 7, it is characterised in that:Every gram of liquid fertilizer preparation In include 50mg urea and 40mg potassium dihydrogen phosphates.
A kind of 9. implantation methods of rare earth asparagus according to claim 7, it is characterised in that:Liquid fertilizer preparation is direct It is sprayed at the surface of culture medium for golden mushroom.
CN201710645201.0A 2017-08-01 2017-08-01 A kind of rare earth culture medium for golden mushroom and implantation methods Pending CN107473790A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109924098A (en) * 2017-12-16 2019-06-25 深圳市环境高新建设有限公司 A kind of arbor transplanting plantation cultural method

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004155900A (en) * 2002-11-06 2004-06-03 Hidekazu Itaka Soil activator using structurized concentrated deep layer water
CN102826909A (en) * 2012-09-14 2012-12-19 江苏维维生物农业科技发展有限公司 White flammulina velutipes culture medium formula
CN104871824A (en) * 2015-06-05 2015-09-02 电白中茂生物科技有限公司 Industrial needle mushroom cultivation method

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004155900A (en) * 2002-11-06 2004-06-03 Hidekazu Itaka Soil activator using structurized concentrated deep layer water
CN102826909A (en) * 2012-09-14 2012-12-19 江苏维维生物农业科技发展有限公司 White flammulina velutipes culture medium formula
CN104871824A (en) * 2015-06-05 2015-09-02 电白中茂生物科技有限公司 Industrial needle mushroom cultivation method

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
张宝林等: "《功能性复混肥料生产工艺技术》", 31 July 2003, 河南科学技术出版社 *
申进文等: "《食用菌生产技术大全》", 31 January 2014, 河南科学技术出版社 *
马占元等: "《日光温室实用技术大全》", 30 September 1997, 河北科学技术出版社 *
鲁剑巍等: "《测土配方与作物配方施肥技术》", 30 June 2006, 金盾出版社 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109924098A (en) * 2017-12-16 2019-06-25 深圳市环境高新建设有限公司 A kind of arbor transplanting plantation cultural method

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