CN110622971A - Efficient compound type selective special herbicide for mulberry seedlings and preparation method thereof - Google Patents

Efficient compound type selective special herbicide for mulberry seedlings and preparation method thereof Download PDF

Info

Publication number
CN110622971A
CN110622971A CN201910862423.7A CN201910862423A CN110622971A CN 110622971 A CN110622971 A CN 110622971A CN 201910862423 A CN201910862423 A CN 201910862423A CN 110622971 A CN110622971 A CN 110622971A
Authority
CN
China
Prior art keywords
herbicide
mulberry
weeds
coniferous
mulberry seedlings
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201910862423.7A
Other languages
Chinese (zh)
Inventor
罗子和
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CN201910862423.7A priority Critical patent/CN110622971A/en
Publication of CN110622971A publication Critical patent/CN110622971A/en
Pending legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/44Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
    • A01N37/48Nitro-carboxylic acids; Derivatives thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N39/00Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
    • A01N39/02Aryloxy-carboxylic acids; Derivatives thereof
    • A01N39/04Aryloxy-acetic acids; Derivatives thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/601,4-Diazines; Hydrogenated 1,4-diazines
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/88Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

The invention discloses a special efficient compound selective herbicide for mulberry seedlings and a preparation method thereof. The invention can kill all the seed reproduction weeds with the height of 10-15cm in mulberry seedlings, and both coniferous weeds and broadleaf weeds can be killed by full plants and roots, the pesticide effect is obvious, the broadleaf weeds can wither in the second day after pesticide spraying and die in 4-6 days, the coniferous weeds can wither in 3-4 days and die in 6-8 days, the invention has little damage to mulberry trees, if the mulberry seedlings have tender shoots, the tender shoots can wither for 2-3 days after pesticide spraying, but the normal growth can be recovered after 2-3 days, and if the tender shoots do not exist, the influence is avoided.

Description

Efficient compound type selective special herbicide for mulberry seedlings and preparation method thereof
Technical Field
The invention relates to the technical field of weeding for mulberry seedling cultivation and the field of weeding for mulberry field management. In particular to a special efficient compound selective herbicide for mulberry seedlings and a preparation method thereof.
Background
The weeding work of mulberry seedling raising and mulberry field management is directly related to success or failure of mulberry seedling raising and mulberry field management. The traditional artificial weeding has low efficiency and high cost, the mulberry seedlings can be damaged in the artificial weeding process of the mulberry seedling nursery, and 3-5% of the mulberry seedlings are pulled out along with the grass; under the conditions of high labor cost and general lack of labor force at present, the requirements of mulberry seedling raising and mulberry field management are no longer met by artificial weeding. In the chemical weeding aspect, two categories of biocidal herbicides and selective herbicides exist. The biocidal herbicide has killing effect on all plants, and can not be sprayed on crops when in use, so that the application range is limited. A single kind of selective herbicide can be sprayed on crops, but the weeding is not thorough and the weeding effect is poor. The selective herbicide is divided into two categories of a conifer herbicide and a broad-leaved weed herbicide, the conifer herbicide is safe for broad-leaved crops and cannot kill the broad-leaved weeds; broadleaf herbicides are safe for coniferous crops and cannot kill coniferous weeds. When one type of weeds is killed while another type of weeds normally grows, the growth of the undecided weeds is accelerated, and therefore, the selective herbicide of a single type has a problem of poor herbicidal effect. The mulberry belongs to broad-leaved plants, the coniferous herbicides are safe to the mulberry, the broad-leaved herbicides have different damage effects on the mulberry to different degrees according to different concentrations and different types, if the coniferous herbicides are only used, broad-leaved weeds cannot be removed, and when the coniferous weeds are killed, the remaining broad-leaved weeds can accelerate growth and have poor weeding effect. The compound herbicide which has high selectivity, can kill coniferous weeds and broadleaf weeds, has little damage to mulberry seedlings (mulberry) and does not influence the normal growth of the mulberry seedlings (mulberry) and has high efficiency and high selectivity is urgently needed in the aspects of mulberry seedling raising and mulberry field management.
Disclosure of Invention
The invention mainly aims to provide a high-efficiency compound type selective special herbicide for mulberry seedlings and a preparation method thereof, which can effectively solve the problems in the background art.
In order to achieve the purpose, the invention adopts the technical scheme that:
a high-efficiency composite selective special herbicide for mulberry seedlings comprises a broadleaf herbicide and a conifer herbicide, wherein the herbicide is a mixture of the broadleaf herbicide and the conifer herbicide.
The broad-leaved grass herbicide is 13% of methoxone sodium aqua, 48% of bentazon aqua and 15% of fluoroglycofen-ethyl emulsion, wherein more than 2 are selected optionally.
The needle-leaf herbicide is 10.8% quizalofop-p-ethyl emulsion, 15% haloxyfop-p-methyl emulsion, 10.8% haloxyfop-ethyl emulsion and 10% cyhalofop-butyl emulsion, wherein 1 or more of the above agents are selected optionally.
A preparation method of a high-efficiency compound type selective special herbicide for mulberry seedlings comprises the following steps:
step 1: 50 liters of water were taken at normal temperature and pressure.
Step 2: adding 30-150 ml of the coniferous herbicide, and fully stirring and mixing with water until the coniferous herbicide is completely dissolved.
And step 3: adding 150 ml of broadleaf weed herbicide, and fully stirring and mixing with water until the broadleaf weed herbicide is completely dissolved.
And 4, step 4: the prepared efficient compound type selective special herbicide for mulberry seedlings is put into spraying equipment for spraying.
Compared with the prior art, the invention has the following remarkable effects:
(1) the invention can kill all the seed reproduction weeds with the height of 10-15cm in mulberry seedlings, and both the coniferous weeds and the broadleaf weeds can be killed by full plants and roots, the pesticide effect is obvious, the broadleaf weeds can be seen to wither in 2 days after pesticide spraying and die in 4-6 days, the coniferous weeds can be seen to wither in 3-4 days and die in 6-8 days.
(2) The invention has little damage to mulberry, if mulberry seedling (mulberry) has tender shoot, the tender shoot will wither for 2-3 days after spraying, but can recover normal growth after 2-3 days, if no tender shoot is existed, the influence is not influenced.
Detailed Description
In order to make the technical means, the creation characteristics, the achievement purposes and the effects of the invention easy to understand, the invention is further described with the specific embodiments.
As shown in the following, the efficient compound type selective special herbicide for mulberry seedlings comprises a broadleaf herbicide and a conifer herbicide, wherein the herbicide is a mixture of the broadleaf herbicide and the conifer herbicide.
Wherein the broad-leaf herbicide is 13% of methoxone sodium aqua, 48% of bentazon aqua and 15% of fluoroglycofen-ethyl emulsion, and optionally more than 2 of the above.
Wherein the needle-leaf herbicide is 10.8% quizalofop-p-ethyl emulsion, 15% haloxyfop-p-ethyl emulsion, 10.8% haloxyfop-p-ethyl emulsion and 10% cyhalofop-butyl emulsion, and 1 or more of the above can be selected optionally.
A preparation method of a high-efficiency compound type selective special herbicide for mulberry seedlings comprises the following steps:
step 1: 50 liters of water were taken at normal temperature and pressure.
Step 2: adding 30-150 ml of the coniferous herbicide, and fully stirring and mixing with water until the coniferous herbicide is completely dissolved.
And step 3: adding 150 ml of broadleaf weed herbicide, and fully stirring and mixing with water until the broadleaf weed herbicide is completely dissolved.
And 4, step 4: the prepared efficient compound type selective special herbicide for mulberry seedlings is put into spraying equipment for spraying.
Example 1
The product is a herbicide screening experiment with 4 mature true leaves of mulberry seedlings as a test object and weeds with the height of 10-15cm as the test object.
(1) 50 liters of water were taken out.
(2) 150 ml of broad-leaved grass herbicide is added, wherein 50 ml of 13% methoxone sodium aqua, 50 ml of 48% bentazon aqua and 50 ml of 15% fluoroglycofen-ethyl emulsion are stirred and fully mixed with water to be dissolved.
(3) 30 ml of a herbicide such as 10.8% quizalofop-p-ethyl emulsion, 10 ml of a 15% haloxyfop-p-ethyl emulsion and 10 ml of a 10.8% haloxyfop-p-ethyl emulsion are added, and the mixture is stirred and fully mixed with water to dissolve the mixture.
(4) The mixed liquid is sprayed on mulberry seedlings (mulberry trees) and weeds, and the result is that: the mulberry seedlings are not damaged, the tender shoots grow normally, wherein the coniferous weeds have a few wilting states on the 5 th day, die a few after 10 days, and the broadleaf weeds have slight wilting states on the 2 nd day, but return to normal growth after the 4 th day. The concentration and the proportion have no harm to mulberry seedlings and have little effect on killing coniferous weeds and broadleaf weeds.
Example 2
The product is a herbicide screening experiment with 4 mature true leaves of mulberry seedlings as a test object and weeds with the height of 10-15cm as the test object.
(1) 50 liters of water were taken out.
(2) 500 ml of broadleaf herbicide, 200 ml of 13% methoxone sodium, 200 ml of 48% bentazon, 100 ml of 15% fluoroglycofen-ethyl, was added and mixed well with water by stirring to dissolve it.
(3) 150 ml of a needle-leaved weed herbicide, 40 ml of 10.8% quizalofop-p-ethyl, 40 ml of 15% haloxyfop-p-methyl, 40 ml of 10.8% haloxyfop-ethyl and 30 ml of 10% cyhalofop-butyl is added, and the mixture is fully mixed with water by stirring to dissolve the mixture.
(4) The mixed liquid is sprayed on mulberry seedlings (mulberry trees) and weeds, and the result is that: the mulberry seedlings are withered seriously on day 2, the death phenomenon is caused on day 4, 40% of the mulberry seedlings die on day 6, and finally the death rate of the mulberry seedlings reaches 70%. The coniferous weeds have a wilting state on day 2, begin to die after day 4, and die totally on day 6. The broadleaf weeds are in a severe wilting state on day 2, death is found on day 3, and all deaths are found on day 5. The concentration and the proportion have the best weeding effect, but have destructive damage to mulberry seedlings.
Example 3
The product is a herbicide screening experiment with 4 mature true leaves of mulberry seedlings as a test object and weeds with the height of 10-15cm as the test object.
(1) 50 liters of water were taken out.
(2) Adding 400 ml of broadleaf weed herbicide, wherein 200 ml of 13% aqueous methoxone solution and 200 ml of 48% aqueous bentazon solution, and fully mixing with water by stirring to dissolve the herbicide.
(3) 100 ml of a herbicide selected from the group consisting of 10.8% quizalofop-p-ethyl (50 ml) and 15% haloxyfop-p-ethyl (50 ml) was added thereto, and the mixture was thoroughly mixed with water by stirring to dissolve the herbicide.
(4) The mixed liquid was sprayed on mulberry seedlings (mulberry trees), and as a result: the mulberry seedlings are withered on day 2, most of the mulberry seedlings return to normal growth on day 5, and a small amount of the mulberry seedlings cannot recover normal growth, so that the mulberry seedlings with poor growth are finally obtained. The coniferous grass plants start to wither after 4 days, die after 6 days, die completely after 8 days, and the broadleaf grass plants start to wither after 2 days, die after 4 days and die completely after 6 days. The concentration and the proportion have good killing effect on both coniferous weeds and broadleaf weeds, but still have great harm to mulberry seedlings.
Example 4
The product is a herbicide screening experiment with 4 mature true leaves of mulberry seedlings as a test object and weeds with the height of 10-15cm as the test object.
(1) 50 liters of water were taken out.
(2) 350 ml of broadleaf herbicide, 200 ml of 13% aqueous methoxone sodium and 150 ml of 48% bentazon are added, and the mixture is fully mixed with water to dissolve the herbicide.
(3) 100 ml of 10.8% haloxyfop-R-methyl is added and dissolved by stirring and mixing with water.
(4) The mixed liquid was sprayed on mulberry seedlings (mulberry trees), and as a result: the shoots of the mulberry seedlings are withered on day 2, but recover on day 4 and all grow normally on day 5. The coniferous weeds have a wilting state on day 4 and all die on day 7. Broadleaf plants appeared severely wilted on day 2, started dying on day 4 and died all on day 6. The mulberry seedling is slightly damaged by the concentration and the proportion, the withered state is only 2-3 days, and the normal growth can be quickly recovered. Has good killing effect on both coniferous weeds and broadleaf weeds.
The solution of example 4 is optimal.
The implementation of the remarks:
(1) and (3) grasping an optimal spraying period: the height of weeds is 10-15cm, and the optimal spraying period is when 80% of mulberry seedlings have 4 mature true leaves. The dosage is the least, the effect is the best, the cost is the lowest, the height of the weeds cannot exceed 15cm, otherwise, the weeding effect is influenced.
(2) In order to ensure the weeding effect, the medicine is required to be prepared and used at present.
(3) The leaf surface can be sprayed only after dew is dried, and rain can not be generated within 8 hours after spraying.
(4) When the weed leaf surface spraying agent is used for spraying, the fog point must be adjusted to be the finest, and the weed leaf surface can be completely sprayed with moisture.
(5) The spraying can not be carried out when drought or waterlogging occurs or the mulberry seedlings grow abnormally.
(6) The fertilizer cannot be applied immediately after the pesticide is sprayed, and the fertilizer is applied in rainy days after the weeds die.
The invention can perfectly solve the problem of low weeding efficiency in the mulberry seedling raising and mulberry field management processes, enables the weeding work of the mulberry seedling raising and mulberry field management to be simple and easy, can reduce the cost of manual weeding and improve the weeding speed and efficiency, and meanwhile, the herbicide has little damage to mulberry seedlings (mulberry trees), has a quick withering state of only 2-3 days, and can restore normal growth. The method can widely improve the seedling rate and success rate of mulberry seedling culture, improve the survival rate of mulberry seedling (mulberry) planting, improve the yield of mulberry gardens, reduce the labor intensity of mulberry seedling culture and mulberry garden management, and achieve the final purpose of improving the economic benefits of mulberry seedling culture and mulberry silkworm breeding.
The foregoing shows and describes the general principles and broad features of the present invention and advantages thereof. It will be understood by those skilled in the art that the present invention is not limited to the embodiments described above, which are described in the specification and illustrated only to illustrate the principle of the present invention, but that various changes and modifications may be made therein without departing from the spirit and scope of the present invention, which fall within the scope of the invention as claimed. The scope of the invention is defined by the appended claims and equivalents thereof.

Claims (4)

1. A high-efficiency compound selective special herbicide for mulberry seedlings is characterized in that: contains broad-leaved grass herbicide and coniferous grass herbicide, and the herbicide is a mixture of the broad-leaved grass herbicide and the coniferous grass herbicide.
2. The efficient compound selective special herbicide for mulberry seedlings according to claim 1, which is characterized in that: the broad-leaf herbicide is 13% of methoxone sodium aqua, 48% of bentazon aqua and 15% of fluoroglycofen-ethyl emulsion, wherein more than 2 are selected optionally.
3. The efficient compound selective special herbicide for mulberry seedlings according to claim 1, which is characterized in that: the needle-leaf herbicide is 10.8 percent of quizalofop-p-ethyl missible oil, 15 percent of haloxyfop-p-butyl missible oil, 10.8 percent of haloxyfop-p-butyl missible oil and 10 percent of cyhalofop-butyl missible oil, wherein 1 or more of the halofop-p-butyl missible oil is selected optionally.
4. A preparation method of a special efficient compound selective herbicide for mulberry seedlings is characterized by comprising the following steps:
step 1: 50 liters of clean water was taken at normal temperature and pressure.
Step 2: adding 30-150 ml of the coniferous herbicide, and fully stirring and mixing with water until the coniferous herbicide is completely dissolved.
And step 3: adding 150 ml of broadleaf weed herbicide, and fully stirring and mixing with water until the broadleaf weed herbicide is completely dissolved.
And 4, step 4: the prepared efficient compound type selective special herbicide for mulberry seedlings is put into spraying equipment for spraying and weeding.
CN201910862423.7A 2019-09-12 2019-09-12 Efficient compound type selective special herbicide for mulberry seedlings and preparation method thereof Pending CN110622971A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910862423.7A CN110622971A (en) 2019-09-12 2019-09-12 Efficient compound type selective special herbicide for mulberry seedlings and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910862423.7A CN110622971A (en) 2019-09-12 2019-09-12 Efficient compound type selective special herbicide for mulberry seedlings and preparation method thereof

Publications (1)

Publication Number Publication Date
CN110622971A true CN110622971A (en) 2019-12-31

Family

ID=68972626

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910862423.7A Pending CN110622971A (en) 2019-09-12 2019-09-12 Efficient compound type selective special herbicide for mulberry seedlings and preparation method thereof

Country Status (1)

Country Link
CN (1) CN110622971A (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102265854A (en) * 2010-06-04 2011-12-07 南京华洲药业有限公司 Weeding composition containing bentazone and haloxyfop-r-methyl, and application thereof
CN102349527A (en) * 2011-07-18 2012-02-15 广西田园生化股份有限公司 Haloxyfop-r-methyl-containing herbicide composition

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102265854A (en) * 2010-06-04 2011-12-07 南京华洲药业有限公司 Weeding composition containing bentazone and haloxyfop-r-methyl, and application thereof
CN102349527A (en) * 2011-07-18 2012-02-15 广西田园生化股份有限公司 Haloxyfop-r-methyl-containing herbicide composition

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
李华英 等: "广西桑树苗圃适用除草剂品种的筛选试验", 《西南农业学报》 *

Similar Documents

Publication Publication Date Title
CN104628481B (en) Fertilizer and pesticide combination reagent for preventing and killing bacterial canker of kivifruit and preparation method of fertilizer and pesticide combination
WO2003090533A1 (en) Plant growth regulating composition for stress- resistance and promoting growth
WO2020103500A1 (en) Twig growth control bactericide composition for citrus and preparation method therefor
CN107455377B (en) Pesticide aqueous solution for promoting plant growth and prolonging effective period of deciduous fruit trees for clearing garden and preparation method thereof
AU2023248153A1 (en) Composition and method of treating bacterial and viral pathogens in plants
KR100480488B1 (en) Control Agents for Powdery Mildew
McWhorter Weed Control in Soybeans by Glyphosate Applied in the Recirculating Sprayer
CN110622971A (en) Efficient compound type selective special herbicide for mulberry seedlings and preparation method thereof
Fangmeier et al. Guayule for rubber production in Arizona
CN104542615A (en) Composition and preparation for preventing and eliminating garden cuscuta plants and applications of composition and preparation
RU2198499C2 (en) Method of protecting fruit trees from spring frosts
Dina Interactions between rate, spray interval and number of applications of the synthetic pyrethroid Decis in cow pea (Vigna unguiculata) pest control
CN115336583B (en) Application of ammonium acetate as fruit tree tip killing agent
CN109076859B (en) Efficient mango planting method
KR101898038B1 (en) Composition for improving grass growth containing salt, a natural material and method for controlling weeds using the composition
Bärring The use of phenoxy herbicides in Swedish Forestry: Amounts, types, and modes of application
US9986736B2 (en) Herbicide compositions and methods for controlling growth of plants of the buckthorn family
Kay Effects of 4-(2, 4-DB) and dalapon on three annual Trifoliums
Bovey Effects of foliarly applied desiccants on selected species under tropical environment
Fisher et al. Control of Three Major Brush Species on Grazing Lands in the United States, Cuba, and Brazil.
Brown Weed investigations
CN116410035A (en) Composition for preventing and treating plant viruses and application thereof
Wallis Herbicides in Kenya coffee IV
CN115997780A (en) Horseradish extract composite medicament
Trew et al. Weed Control in Cultivated Pastures and Meadows.

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20191231