CN105819997A - Corn culture medium and preparation method thereof - Google Patents
Corn culture medium and preparation method thereof Download PDFInfo
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- CN105819997A CN105819997A CN201610303816.0A CN201610303816A CN105819997A CN 105819997 A CN105819997 A CN 105819997A CN 201610303816 A CN201610303816 A CN 201610303816A CN 105819997 A CN105819997 A CN 105819997A
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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
- C05G3/00—Mixtures of one or more fertilisers with additives not having a specially fertilising activity
- C05G3/60—Biocides or preservatives, e.g. disinfectants, pesticides or herbicides; Pest repellants or attractants
-
- 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
- A01G24/00—Growth substrates; Culture media; Apparatus or methods therefor
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05C—NITROGENOUS FERTILISERS
- C05C11/00—Other nitrogenous fertilisers
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- Life Sciences & Earth Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plant Pathology (AREA)
- Environmental Sciences (AREA)
- Fertilizers (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
The invention discloses a corn culture medium and a preparation method thereof. The corn culture medium is prepared from, by weight, 10-20 parts of vinegar residues, 20-40 parts of farmyard manure, 20-40 parts of common nostoc, 15-20 parts of red date tree leaves, 5-10 parts of iron vitriol, 10-20 parts of bagasse, 10-15 parts of corn stalk powder, 1-5 parts of duckweed, 3-6 parts of waste lime peel, 3-6 parts of durian shells, 0.5-1.5 parts of calcium amino acid chelate, 1-3 parts of thermophilic bacillus licheniformis, 2-6 parts of bacillus subtilis, 1-5 parts of corynebacterium glutamicum, 3-5 parts of trichoderma virens, 1-3 parts of Saccharomyces cerevisiae YB strains, 6-10 parts of rice endophytic bacteria and 5-10 parts of vermiculite. The corn culture medium is high in nutrient content and easy to process, the majority of the raw materials are waste and residues produced in life or production process, and energy conservation, emission reduction and agricultural recycling economy are achieved.
Description
Technical field
The present invention relates to maize culture field, be specifically related to a kind of corn culture medium matter and preparation method thereof.
Background technology
Semen Maydis is to be distributed one of widest cereal crops in the world, and cultivated area is only second to Semen Tritici aestivi and Oryza sativa L. and occupies the 3rd.Planting range from north latitude 58 ° (Canada and Russia) to 40 ° of south latitude (South America), Semen Maydis plays an important role in China's grain security, it it is important forage crop, it it is again the important source material of the industries such as food, chemical industry, fuel, medicine, therefore, its importance gets most of the attention.
Along with developing rapidly of corn planting technology, cultivation technique without soil and seedling-raising technique obtain large area, on a large scale popularization and application, the demand of soilless raising seedling substrate increases day by day；Rock wool, the peat composed of rotten mosses are the base materials of the seedling medium being most frequently with in soilless culture; but cost is high; in recent years, along with the mankind are to sustainable development and the understanding of the importance of environmental conservation, in the selection of base starting material; with producing refuse or residue the replacement peat composed of rotten mosses, rock wool etc. in life or in production process; having become as the main trend of world development, the raw material of this kind of substrate has renewable, wide advantage of originating, and its nutritional labeling is high; processing cost is low, easy to use.
Summary of the invention
For solving the problems referred to above, the invention provides garbage, residue that a kind of corn culture medium matter and preparation method thereof, nutritional labeling height, it is easy to processing, and major part raw material are in life or produce in production process, it is achieved that energy-saving and emission-reduction and Agricultural recycling economy.
For achieving the above object, the technical scheme that the present invention takes is:
A kind of corn culture medium matter, is prepared from by the raw material of following weight portion:
Vinegar 10～20 parts, farm manure 20～40 parts, Nostoc 20～40 parts, Fructus Jujubae leaves 15～20 parts, ferrous sulfate heptahydrate 5～10 parts, bagasse 10～20 parts, corn stalk powder 10～15 parts, Herba Spirodelae 1～5 parts, discarded blue or green lemon skin 3～6 parts, durian shell 3～6 parts, calcium amino acid chelate 0.5～1.5 parts, thermophilic Bacillus licheniformis 1～3 parts, bacillus subtilis microbial agent 2～6 parts, Corynebacterium glutamicum 1～5 parts, green trichoderma 3～5 parts, saccharomyces cerevisiae YB bacterial strain 1～3 parts, Rice Endophytic Bacteria 6～10 parts, Vermiculitum 5～10 parts.
Preferably, the raw material of following weight portion it is prepared from:
Vinegar 10 parts, farm manure 20 parts, Nostoc 20 parts, Fructus Jujubae leaves 15 parts, ferrous sulfate heptahydrate 5 parts, bagasse 10 parts, corn stalk powder 10 parts, 1 part of Herba Spirodelae, discarded blue or green lemon skin 3 parts, durian shell 3 parts, calcium amino acid chelate 0.5 part, thermophilic Bacillus licheniformis 1 part, bacillus subtilis microbial agent 2 parts, Corynebacterium glutamicum 1 part, green trichoderma 3 parts, saccharomyces cerevisiae YB bacterial strain 1 part, Rice Endophytic Bacteria 6 parts, Vermiculitum 5 parts.
Preferably, the raw material of following weight portion it is prepared from:
Vinegar 20 parts, farm manure 40 parts, Nostoc 40 parts, Fructus Jujubae leaves 20 parts, ferrous sulfate heptahydrate 10 parts, bagasse 20 parts, corn stalk powder 15 parts, 5 parts of Herba Spirodelae, discarded blue or green lemon skin 6 parts, durian shell 6 parts, calcium amino acid chelate 1.5 parts, thermophilic Bacillus licheniformis 3 parts, bacillus subtilis microbial agent 6 parts, Corynebacterium glutamicum 5 parts, green trichoderma 5 parts, saccharomyces cerevisiae YB bacterial strain 3 parts, Rice Endophytic Bacteria 10 parts, Vermiculitum 10 parts.
Preferably, the raw material of following weight portion it is prepared from:
Vinegar 15 parts, farm manure 30 parts, Nostoc 30 parts, Fructus Jujubae leaves 17.5 parts, ferrous sulfate heptahydrate 7.5 parts, bagasse 15 parts, corn stalk powder 12.5 parts, 3 parts of Herba Spirodelae, discarded blue or green lemon skin 4.5 parts, durian shell 4.5 parts, calcium amino acid chelate 1 part, thermophilic Bacillus licheniformis 2 parts, bacillus subtilis microbial agent 4 parts, Corynebacterium glutamicum 3 parts, green trichoderma 4 parts, saccharomyces cerevisiae YB bacterial strain 2 parts, Rice Endophytic Bacteria 8 parts, Vermiculitum 7.5 parts.
The preparation method of above-mentioned a kind of corn culture medium matter, comprises the steps:
S1, weighing vinegar 10～20 parts, Nostoc 20～40 parts, Fructus Jujubae leaves 15～20 parts, bagasse 10～20 parts, corn stalk powder 10～15 parts, Herba Spirodelae 1～5 parts, discarded blue or green lemon skin 3～6 parts, durian shell 3～6 parts and be placed in steam-explosion jar, being first passed through nitrogen to steam explosion pressure inside the tank is 0.5～1.1MPa. explosion treatment 12～26min；Being passed through the most rapidly steam to steam explosion pressure inside the tank is 1.1～1.6MPa, Steam explosion treatment 1.9～3.1min, after being cooled to room temperature, inoculate thermophilic Bacillus licheniformis 1～3 parts, bacillus subtilis microbial agent 2～6 parts, Corynebacterium glutamicum 1～5 parts, temperature 30～40 DEG C, ferment at constant temperature 49～56 hours, obtain fermentation liquid；
S2, weigh farm manure 20～40 parts, ferrous sulfate heptahydrate 5～10 parts, calcium amino acid chelate 0.5～1.5 parts be placed in high-speed mixer in stirring be sufficiently mixed rear discharging, obtain mixture；
S3, weigh green trichoderma 3～5 parts, saccharomyces cerevisiae YB bacterial strain 1～3 parts, Rice Endophytic Bacteria 6～10 parts, spray into after Vermiculitum 5～10 parts of mixed dilutings 3～5 times in the mixture of step S2 gained and mix, the fermentation liquid of step S1 gained is sprayed onto on raw material simultaneously and turns mix homogeneously, spray the most weekly 1 time, turn and be formed uniformly stable bacterium colony body, vaccinization 4～make after 5 weeks mixture enter catabolic phase, stop decomposer inoculation, 1 raw material is turned again every 5 days, continue 4～5 weeks, keep the aerobic conditions in stockpile, stockpile humidity is maintained at 70%～80%, obtain culture matrix.
The method have the advantages that
Substrate can be made to be in a pH value being more suitable for plant growth all the time, by crop material powder and the interpolation of Nostoc, improve aeration and the retentiveness of substrate, not only can significantly reduce the leaching loss phenomenon of fertilizer, extending fertilizer efficiency and improve utilization rate of fertilizer, its abundant hole can be effectively increased substrate microorganism living environment and quantity；On the one hand the interpolation of discarded blue or green lemon skin can increase the content of modifying agent humus, and on the other hand its a large amount of citric acids contained can promote the chelation of slaine and fermentation liquid, generates the multiple Chelating state nutrient being prone to plant absorption, increases soil fertility；Durian shell and the interpolation of vinegar, enrich the nutritional labeling of substrate further, the present invention is by rationally selecting microbial inoculum and proportioning simultaneously, nutritional labeling in raw material can be fully dissolved out, so that crop can fully absorb nutrition, adding yield, can well be suppressed the pest and disease damage of substrate by the interpolation of Fructus Jujubae leaves, the present invention can be additionally used in the field of planting such as Semen Tritici aestivi, Sorghum vulgare Pers., Semen sojae atricolor, Semen arachidis hypogaeae.
Detailed description of the invention
In order to make objects and advantages of the present invention clearer, below in conjunction with embodiment, the present invention is further elaborated.Should be appreciated that specific embodiment described herein, only in order to explain the present invention, is not intended to limit the present invention.
Test method used in embodiment if no special instructions, is conventional method；The material that used, reagent etc., if no special instructions, all can have been bought from biological reagent company by commercial sources.
Embodiment 1
S1, weigh vinegar 10 parts, Nostoc 20 parts, Fructus Jujubae leaves 15 parts, bagasse 10 parts, corn stalk powder 10 parts, 1 part of Herba Spirodelae, discarded blue or green lemon skin 3 parts, durian shell 3 parts are placed in steam-explosion jar, first being passed through nitrogen to steam explosion pressure inside the tank is 0.5MPa, explosion treatment 26min；Being passed through the most rapidly steam to steam explosion pressure inside the tank is 1.1MPa, and Steam explosion treatment 3.1min, after being cooled to room temperature, inoculate thermophilic Bacillus licheniformis 1 part, bacillus subtilis microbial agent 2 parts, Corynebacterium glutamicum 1 part, temperature 30 DEG C, ferment at constant temperature 49 hours, obtain fermentation liquid；
S2, weigh farm manure 20 parts, in ferrous sulfate heptahydrate 5 parts, calcium amino acid chelate are placed in high-speed mixer stirring be sufficiently mixed rear discharging, obtain mixture；
S3, weigh green trichoderma 3 parts, saccharomyces cerevisiae YB bacterial strain 1 part, Rice Endophytic Bacteria 6～10 parts, spray into after 5 parts of mixed dilutings of Vermiculitum 3 times in the mixture of step S2 gained and mix, the fermentation liquid of step S1 gained is sprayed onto on raw material simultaneously and turns mix homogeneously, spray the most weekly 1 time, turn and be formed uniformly stable bacterium colony body, vaccinization 4～make after 5 weeks mixture enter catabolic phase, stop decomposer inoculation, 1 raw material is turned again every 5 days, continue 4～5 weeks, keep the aerobic conditions in stockpile, stockpile humidity is maintained at 70%～80%, obtain culture matrix.
Embodiment 2
S1, weigh vinegar 20 parts, Nostoc 40 parts, Fructus Jujubae leaves 20 parts, bagasse 20 parts, corn stalk powder 15 parts, 5 parts of Herba Spirodelae, discarded blue or green lemon skin 6 parts, durian shell 6 parts are placed in steam-explosion jar, first being passed through nitrogen to steam explosion pressure inside the tank is 01.1MPa, explosion treatment 12min；Being passed through the most rapidly steam to steam explosion pressure inside the tank is 1.6MPa, and Steam explosion treatment 1.9min, after being cooled to room temperature, inoculate thermophilic Bacillus licheniformis 3 parts, bacillus subtilis microbial agent 6 parts, Corynebacterium glutamicum 5 parts, temperature 40 DEG C, ferment at constant temperature 56 hours, obtain fermentation liquid；
S2, weigh farm manure 40 parts, in ferrous sulfate heptahydrate 10 parts, calcium amino acid chelate 1.5 parts are placed in high-speed mixer stirring be sufficiently mixed rear discharging, obtain mixture；
S3, weigh green trichoderma 5 parts, saccharomyces cerevisiae YB bacterial strain 3 parts, Rice Endophytic Bacteria 10 parts, spray into after 10 parts of mixed dilutings of Vermiculitum 5 times in the mixture of step S2 gained and mix, the fermentation liquid of step S1 gained is sprayed onto on raw material simultaneously and turns mix homogeneously, spray the most weekly 1 time, turn and be formed uniformly stable bacterium colony body, vaccinization 4～make after 5 weeks mixture enter catabolic phase, stop decomposer inoculation, 1 raw material is turned again every 5 days, continue 4～5 weeks, keep the aerobic conditions in stockpile, stockpile humidity is maintained at 70%～80%, obtain culture matrix.
Embodiment 3
S1, weigh vinegar 15 parts, Nostoc 30 parts, Fructus Jujubae leaves 17.5 parts, bagasse 15 parts, corn stalk powder 12.5 parts, 3 parts of Herba Spirodelae, discarded blue or green lemon skin 4.5 parts, durian shell 4.5 parts are placed in steam-explosion jar, first being passed through nitrogen to steam explosion pressure inside the tank is 0.8MPa, explosion treatment 19min；Being passed through the most rapidly steam to steam explosion pressure inside the tank is 1.35MPa, and Steam explosion treatment 2.5min, after being cooled to room temperature, inoculate thermophilic Bacillus licheniformis 2 parts, bacillus subtilis microbial agent 4 parts, Corynebacterium glutamicum 3 parts, temperature 35 DEG C, ferment at constant temperature 52.5 hours, obtain fermentation liquid；
S2, weigh farm manure 30 parts, in ferrous sulfate heptahydrate 7.5 parts, calcium amino acid chelate 1 part are placed in high-speed mixer stirring be sufficiently mixed rear discharging, obtain mixture；
S3, weigh green trichoderma 4 parts, saccharomyces cerevisiae YB bacterial strain 2 parts, Rice Endophytic Bacteria 8 parts, spray into after 7.5 parts of mixed dilutings of Vermiculitum 4 times in the mixture of step S2 gained and mix, the fermentation liquid of step S1 gained is sprayed onto on raw material simultaneously and turns mix homogeneously, spray the most weekly 1 time, turn and be formed uniformly stable bacterium colony body, vaccinization 4～make after 5 weeks mixture enter catabolic phase, stop decomposer inoculation, 1 raw material is turned again every 5 days, continue 4～5 weeks, keep the aerobic conditions in stockpile, stockpile humidity is maintained at 70%～80%, obtain culture matrix.
The above is only the preferred embodiment of the present invention; it should be pointed out that, for those skilled in the art, under the premise without departing from the principles of the invention; can also make some improvements and modifications, these improvements and modifications also should be regarded as protection scope of the present invention.
Claims (5)
1. a corn culture medium matter, it is characterised in that be prepared from by the raw material of following weight portion:
Vinegar 10～20 parts, farm manure 20～40 parts, Nostoc 20～40 parts, Fructus Jujubae leaves 15～20 parts, ferrous sulfate heptahydrate 5～10 parts, bagasse 10～20 parts, corn stalk powder 10～15 parts, Herba Spirodelae 1～5 parts, discarded blue or green lemon skin 3～6 parts, durian shell 3～6 parts, calcium amino acid chelate 0.5～1.5 parts, thermophilic Bacillus licheniformis 1～3 parts, bacillus subtilis microbial agent 2～6 parts, Corynebacterium glutamicum 1～5 parts, green trichoderma 3～5 parts, saccharomyces cerevisiae YB bacterial strain 1～3 parts, Rice Endophytic Bacteria 6～10 parts, Vermiculitum 5～10 parts.
2. a kind of corn culture medium matter as claimed in claim 1, it is characterised in that be prepared from by the raw material of following weight portion:
Vinegar 10 parts, farm manure 20 parts, Nostoc 20 parts, Fructus Jujubae leaves 15 parts, ferrous sulfate heptahydrate 5 parts, bagasse 10 parts, corn stalk powder 10 parts, 1 part of Herba Spirodelae, discarded blue or green lemon skin 3 parts, durian shell 3 parts, calcium amino acid chelate 0.5 part, thermophilic Bacillus licheniformis 1 part, bacillus subtilis microbial agent 2 parts, Corynebacterium glutamicum 1 part, green trichoderma 3 parts, saccharomyces cerevisiae YB bacterial strain 1 part, Rice Endophytic Bacteria 6 parts, Vermiculitum 5 parts.
3. a kind of corn culture medium matter as claimed in claim 1, it is characterised in that be prepared from by the raw material of following weight portion:
Vinegar 20 parts, farm manure 40 parts, Nostoc 40 parts, Fructus Jujubae leaves 20 parts, ferrous sulfate heptahydrate 10 parts, bagasse 20 parts, corn stalk powder 15 parts, 5 parts of Herba Spirodelae, discarded blue or green lemon skin 6 parts, durian shell 6 parts, calcium amino acid chelate 1.5 parts, thermophilic Bacillus licheniformis 3 parts, bacillus subtilis microbial agent 6 parts, Corynebacterium glutamicum 5 parts, green trichoderma 5 parts, saccharomyces cerevisiae YB bacterial strain 3 parts, Rice Endophytic Bacteria 10 parts, Vermiculitum 10 parts.
4. a kind of corn culture medium matter as claimed in claim 1, it is characterised in that be prepared from by the raw material of following weight portion:
Vinegar 15 parts, farm manure 30 parts, Nostoc 30 parts, Fructus Jujubae leaves 17.5 parts, ferrous sulfate heptahydrate 7.5 parts, bagasse 15 parts, corn stalk powder 12.5 parts, 3 parts of Herba Spirodelae, discarded blue or green lemon skin 4.5 parts, durian shell 4.5 parts, calcium amino acid chelate 1 part, thermophilic Bacillus licheniformis 2 parts, bacillus subtilis microbial agent 4 parts, Corynebacterium glutamicum 3 parts, green trichoderma 4 parts, saccharomyces cerevisiae YB bacterial strain 2 parts, Rice Endophytic Bacteria 8 parts, Vermiculitum 7.5 parts.
5. the preparation method of a kind of corn culture medium matter as described in any one of claims 1 to 3, it is characterised in that comprise the steps:
S1, weigh vinegar 10～20 parts, Nostoc 20～40 parts, Fructus Jujubae leaves 15～20 parts, bagasse 10～20 parts, corn stalk powder 10～15 parts, Herba Spirodelae 1～5 parts, discarded blue or green lemon skin 3～6 parts, durian shell 3～6 parts and be placed in steam-explosion jar, first being passed through nitrogen to steam explosion pressure inside the tank is 0.5～1.1MPa, explosion treatment 12～26min；Being passed through the most rapidly steam to steam explosion pressure inside the tank is 1.1～1.6MPa, Steam explosion treatment 1.9～3.1min, after being cooled to room temperature, inoculate thermophilic Bacillus licheniformis 1～3 parts, bacillus subtilis microbial agent 2～6 parts, Corynebacterium glutamicum 1～5 parts, temperature 30～40 DEG C, ferment at constant temperature 49～56 hours, obtain fermentation liquid；
S2, weigh farm manure 20～40 parts, ferrous sulfate heptahydrate 5～10 parts, calcium amino acid chelate 0.5～1.5 parts be placed in high-speed mixer in stirring be sufficiently mixed rear discharging, obtain mixture；
S3, weigh green trichoderma 3～5 parts, saccharomyces cerevisiae YB bacterial strain 1～3 parts, Rice Endophytic Bacteria 6～10 parts, spray into after Vermiculitum 5～10 parts of mixed dilutings 3～5 times in the mixture of step S2 gained and mix, the fermentation liquid of step S1 gained is sprayed onto on raw material simultaneously and turns mix homogeneously, spray the most weekly 1 time, turn and be formed uniformly stable bacterium colony body, vaccinization 4～make after 5 weeks mixture enter catabolic phase, stop decomposer inoculation, 1 raw material is turned again every 5 days, continue 4～5 weeks, keep the aerobic conditions in stockpile, stockpile humidity is maintained at 70%～80%, obtain culture matrix.
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| Application Number | Priority Date | Filing Date | Title |
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| CN201610303816.0A CN105819997A (en) | 2016-05-10 | 2016-05-10 | Corn culture medium and preparation method thereof |
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| CN201610303816.0A CN105819997A (en) | 2016-05-10 | 2016-05-10 | Corn culture medium and preparation method thereof |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106365774A (en) * | 2016-08-23 | 2017-02-01 | 内蒙古农业大学 | Water-soluble quick-acting drop irrigation fertilizer |
| CN106386112A (en) * | 2016-08-31 | 2017-02-15 | 北海市农业科学研究所 | Cowpea planting method capable of improving quality of cowpea |
| CN106386056A (en) * | 2016-08-31 | 2017-02-15 | 山西省农业科学院高寒区作物研究所 | Cultivation method for potatoes |
| CN109287409A (en) * | 2018-11-26 | 2019-02-01 | 安徽省农业科学院烟草研究所 | A method of it is prepared using fresh edible maize seedbed and improves culturing and transplanting seedlings survival rate |
| CN111543230A (en) * | 2020-03-30 | 2020-08-18 | 同济大学 | Large-scale blueberry planting method suitable for mountainous regions |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103058725A (en) * | 2013-01-25 | 2013-04-24 | 河南农业大学 | Method for quickly producing bio-organic fertilizer by using tobacco stalks and bio-organic fertilizer |
| CN104710237A (en) * | 2015-02-14 | 2015-06-17 | 李德新 | Corn culture substrate and preparation method thereof |
| CN104744090A (en) * | 2015-03-25 | 2015-07-01 | 杨健 | Method and device for preparing novel ecological culture medium from municipal waste |
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2016
- 2016-05-10 CN CN201610303816.0A patent/CN105819997A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103058725A (en) * | 2013-01-25 | 2013-04-24 | 河南农业大学 | Method for quickly producing bio-organic fertilizer by using tobacco stalks and bio-organic fertilizer |
| CN104710237A (en) * | 2015-02-14 | 2015-06-17 | 李德新 | Corn culture substrate and preparation method thereof |
| CN104744090A (en) * | 2015-03-25 | 2015-07-01 | 杨健 | Method and device for preparing novel ecological culture medium from municipal waste |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106365774A (en) * | 2016-08-23 | 2017-02-01 | 内蒙古农业大学 | Water-soluble quick-acting drop irrigation fertilizer |
| CN106386112A (en) * | 2016-08-31 | 2017-02-15 | 北海市农业科学研究所 | Cowpea planting method capable of improving quality of cowpea |
| CN106386056A (en) * | 2016-08-31 | 2017-02-15 | 山西省农业科学院高寒区作物研究所 | Cultivation method for potatoes |
| CN106386056B (en) * | 2016-08-31 | 2021-06-15 | 山西省农业科学院高寒区作物研究所 | Potato cultivation method |
| CN109287409A (en) * | 2018-11-26 | 2019-02-01 | 安徽省农业科学院烟草研究所 | A method of it is prepared using fresh edible maize seedbed and improves culturing and transplanting seedlings survival rate |
| CN111543230A (en) * | 2020-03-30 | 2020-08-18 | 同济大学 | Large-scale blueberry planting method suitable for mountainous regions |
| CN111543230B (en) * | 2020-03-30 | 2021-09-14 | 同济大学 | Large-scale blueberry planting method suitable for mountainous regions |
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Application publication date: 20160803 |