CN115886007B - Pesticide composition, application thereof and pesticide preparation containing pesticide composition - Google Patents
Pesticide composition, application thereof and pesticide preparation containing pesticide composition Download PDFInfo
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- CN115886007B CN115886007B CN202211360673.9A CN202211360673A CN115886007B CN 115886007 B CN115886007 B CN 115886007B CN 202211360673 A CN202211360673 A CN 202211360673A CN 115886007 B CN115886007 B CN 115886007B
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- pyrethroid
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- pesticide composition
- bemisia tabaci
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- 239000000575 pesticide Substances 0.000 title claims abstract description 45
- 239000000203 mixture Substances 0.000 title claims abstract description 43
- 238000002360 preparation method Methods 0.000 title description 19
- 239000002728 pyrethroid Substances 0.000 claims abstract description 20
- 239000005892 Deltamethrin Substances 0.000 claims abstract description 11
- 229960002483 decamethrin Drugs 0.000 claims abstract description 11
- OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 claims abstract description 11
- KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical group CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 claims abstract description 8
- 241000254127 Bemisia tabaci Species 0.000 claims description 24
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 18
- 238000009472 formulation Methods 0.000 claims description 14
- FYQGBXGJFWXIPP-UHFFFAOYSA-N hydroprene Chemical compound CCOC(=O)C=C(C)C=CCC(C)CCCC(C)C FYQGBXGJFWXIPP-UHFFFAOYSA-N 0.000 claims description 14
- 229930000073 hydroprene Natural products 0.000 claims description 14
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- 239000004299 sodium benzoate Substances 0.000 description 4
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- SNAAJJQQZSMGQD-UHFFFAOYSA-N aluminum magnesium Chemical compound [Mg].[Al] SNAAJJQQZSMGQD-UHFFFAOYSA-N 0.000 description 2
- 210000003169 central nervous system Anatomy 0.000 description 2
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- -1 diester bromocyanides Chemical class 0.000 description 2
- YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 2
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- 102000012440 Acetylcholinesterase Human genes 0.000 description 1
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- 244000144730 Amygdalus persica Species 0.000 description 1
- 240000007124 Brassica oleracea Species 0.000 description 1
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
- 240000008574 Capsicum frutescens Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241001414720 Cicadellidae Species 0.000 description 1
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- 235000015001 Cucumis melo var inodorus Nutrition 0.000 description 1
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- 241000255925 Diptera Species 0.000 description 1
- 208000030453 Drug-Related Side Effects and Adverse reaction Diseases 0.000 description 1
- 239000005906 Imidacloprid Substances 0.000 description 1
- 239000005797 Iprovalicarb Substances 0.000 description 1
- NWUWYYSKZYIQAE-ZBFHGGJFSA-N L-(R)-iprovalicarb Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C1=CC=C(C)C=C1 NWUWYYSKZYIQAE-ZBFHGGJFSA-N 0.000 description 1
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- 241000935974 Paralichthys dentatus Species 0.000 description 1
- 206010033799 Paralysis Diseases 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 241000758706 Piperaceae Species 0.000 description 1
- 235000006040 Prunus persica var persica Nutrition 0.000 description 1
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 description 1
- 108010052164 Sodium Channels Proteins 0.000 description 1
- 102000018674 Sodium Channels Human genes 0.000 description 1
- 240000004460 Tanacetum coccineum Species 0.000 description 1
- 239000005941 Thiamethoxam Substances 0.000 description 1
- 241001414989 Thysanoptera Species 0.000 description 1
- 206010070863 Toxicity to various agents Diseases 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- ROVGZAWFACYCSP-MQBLHHJJSA-N [2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-MQBLHHJJSA-N 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229940022698 acetylcholinesterase Drugs 0.000 description 1
- LRZWFURXIMFONG-HRSIRGMGSA-N afidopyropen Chemical compound C([C@@]1(C)[C@H]2[C@]([C@H]3[C@@H](O)C=4C(=O)OC(=CC=4O[C@]3(C)[C@@H](O)C2)C=2C=NC=CC=2)(C)CC[C@@H]1OC(=O)C1CC1)OC(=O)C1CC1 LRZWFURXIMFONG-HRSIRGMGSA-N 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 238000012271 agricultural production Methods 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
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- 230000009286 beneficial effect Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000001390 capsicum minimum Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
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- 235000013399 edible fruits Nutrition 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 description 1
- 229940056881 imidacloprid Drugs 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000004530 micro-emulsion Substances 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 210000000653 nervous system Anatomy 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000003090 pesticide formulation Substances 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 1
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 1
- 229940015367 pyrethrum Drugs 0.000 description 1
- 238000000611 regression analysis Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
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- 239000007921 spray Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000004548 suspo-emulsion Substances 0.000 description 1
- 239000012747 synergistic agent Substances 0.000 description 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
- 231100000820 toxicity test Toxicity 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
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- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
The invention provides a pesticide composition, which comprises a dicycloprid and pyrethroid pesticide; the pyrethroid pesticide is selected from beta-cypermethrin or deltamethrin, and the weight ratio of the beta-propisochlor to the pyrethroid pesticide is 1-20:0.1-20. The composition has obvious synergistic effect, can effectively reduce the dosage of active ingredients, slow down the generation of drug resistance of pests, lighten environmental pollution and ensure food safety.
Description
Technical Field
The invention relates to the field of agrochemistry, in particular to a pesticide composition, application thereof and a pesticide preparation containing the same.
Background
Bemisia tabaci is commonly called as white moth, has a very wide host range, and can harm various crops such as tomatoes, cucumbers, peppers and the like. Primary in tropical and subtropical regions, today spread rapidly throughout the world. The adult body length of the bemisia tabaci is less than 1mm, but the damage caused by the bemisia tabaci is not ignored. Bemisia tabaci directly pierces plant juice, so that the plant is weakened, nymphs and adults can also secrete honeydew, and the generation of coal pollution is induced. When the density is high, the leaves are black, the photosynthesis is seriously affected, and in addition, more than 70 virus diseases can be transmitted on 30 crops by the bemisia tabaci.
Wheat aphids commonly called oil worms and aphid can carry out piercing and sucking harm on wheat, influence photosynthesis and nutrition absorption and transmission of the wheat, basically occur in a wheat planting area, have light and heavy occurrence degree, and bring no small influence on the yield and quality of the wheat. The common pesticide for preventing and controlling wheat aphids is, for example, thiamethoxam, imidacloprid and other nicotinic pesticides, and the action mechanism is to destroy the function of a nervous system by interacting with a sodium ion channel of the pest, inhibit nicotinic acid acetylcholinesterase receptors of the central nervous system of the pest, block normal conduction of the central nervous system of the pest, and cause paralysis of the pest to cause death.
At present, the use of pesticides in the control of bemisia tabaci and aphids is still dominant. Because of the use of single pesticides throughout the year, the pests can generate strong resistance, and in this case, the pesticides need to be replaced in time for control.
The common name of the hydroprene is: afidopyropen which has novel structure and brand new action mechanism, can be used for preventing and controlling small pests such as scale insects, thrips, leafhoppers, whiteflies and the like on rice, fruit trees, vegetables, intertillage crops and ornamental plants, has good effect on leaf surface treatment, seed treatment and soil treatment, and has low toxicity. The novel pesticide has a unique action mechanism, so that the novel pesticide is very suitable for pest control which generates drug resistance or is easy to generate drug resistance, but the raw material price of the hydroprene is higher, the popularization is not facilitated, and the problem that drug resistance can be generated after long-term single use is also existed.
The pyrethroid insecticide is a novel broad-spectrum insecticide which is synthesized artificially on the basis of simulating the active ingredients of natural pyrethrum and has the advantages of high efficiency, low toxicity, low residue and safety. The pesticide has the advantages of high knockdown speed, strong knockdown force, small dosage and rain wash resistance after spraying, and is an ideal substitute for traditional organic chlorine and organic phosphorus pesticides. The pyrethroid pesticide can prevent and treat lepidoptera, homoptera, diptera, orthoptera and coleoptera pests, and has good effect on lepidoptera and homoptera pests. But due to their large use, many pests develop resistance to them.
The applicant screens out the insecticidal composition with synergistic effect by researching the compound combination of the bifenthrin and different pyrethroid medicines.
Disclosure of Invention
In order to solve the above problems, a first aspect of the present invention provides a pesticidal composition comprising a dicycloprid and a pyrethroid pesticide; the pyrethroid pesticide is selected from beta-cypermethrin or deltamethrin, and the weight ratio of the beta-propisochlor to the pyrethroid pesticide is 1-20:0.1-20.
The weight ratio of the preferred hydroprene to the pyrethroid pesticide is 1-10:0.2-10.
The weight ratio of the preferred hydroprene to the beta-cypermethrin is 1:2.5-1:2; the weight ratio of the dicycloprid to the deltamethrin is 1:1-2.5:1.
The second aspect provides a pesticide preparation, which comprises the pesticide composition, wherein the weight percentage of active ingredients is 1-50%, and the formulation of the pesticide preparation is one of wettable powder, water dispersible granules, suspending agent, aqueous emulsion, microemulsion, suspoemulsion, microcapsule suspending agent and dispersible agent.
In a second aspect there is provided the use of a pesticide composition or pesticide formulation for controlling crop pests. The pests are bemisia tabaci, aphids, plasmaphis and other pests; the crops are tomato, capsicum, cucumber, wheat, cabbage, cucumber, peach, apple tree and other plants.
The invention has at least one of the following beneficial effects:
The invention ensures excellent pest control effect and simultaneously controls the raw material cost by compounding the hydroprene and pyrethroid pesticides, thereby being easier to be widely popularized in agricultural production.
The composition has obvious synergistic effect, can effectively reduce the dosage of active ingredients, slows down the generation of drug resistance of pests such as tomato bemisia tabaci, reduces environmental pollution and ensures food safety.
The dispersible agent is added with the synergist methyl oleate, so that the control effect of the dispersible agent preparation on pests can be improved; in particular, the methyl oleate promotes the remarkable improvement of the prevention effect of the 3% diester-cyanuric chloride dispersible agent, and has remarkable variability.
Detailed Description
The invention is further illustrated with reference to specific embodiments.
Example 1: indoor toxicity test of hydroprene and pyrethroid compound combination on bemisia tabaci
Test material: tomato type B bemisia tabaci is collected from a greenhouse population in a tomato test field, and is cultivated and stored indoors, and bemisia tabaci adults with consistent individual sizes are selected for testing during experiments.
The testing method comprises the following steps: the blade impregnation method is adopted. On a pre-test basis, the test agents were diluted to 7 series of concentrations. Beating fresh tomato leaves into leaf discs by using a puncher with the diameter of 2.5cm, immersing the leaves in the liquid medicine for 10s, placing the leaves on absorbent paper for airing, and clamping the leaves into glass tubes which are added with 1mL of agar in advance by using tweezers, wherein each tube is 1 piece; sucking the adult bemisia tabaci to be tested into a fluke device, transferring the device into a glass tube, repeating the treatment for 4 times, sealing the glass tube with a cotton plug for 30-40 times, inverting the glass tube into a artificial climate box, counting and checking the death number of the bemisia tabaci after 48 hours, and calculating the death rate by taking the case that the light touch body of the writing brush tip cannot be regarded as death by a crawler.
Regression analysis is carried out on the treatment concentration log values and the corresponding mortality probability values of the single agents and the mixed and combined agents with different proportions by using DPS statistical software, a virulence regression curve, LC 50 values and correlation coefficients are calculated, and the co-virulence coefficient (CTC value) of the mixture is calculated according to the grand Yunpei method.
The co-toxicity coefficient (CTC value) of the mixture is calculated according to the formulas (1), (2) and (3):
Wherein: ati—actual measured virulence index of the mixture;
S-LC 50 for standard pesticides in milligrams per liter (mg/L);
LC 50 for M-blends in milligrams per liter (mg/L).
TTI=A×PA+B×PB·························(2)
Wherein: TTI-the theoretical toxicity index of the mixture;
a-a agent virulence index;
The percentage of the P A -A medicament in the mixture is expressed as percentage (%);
B-B drug toxicity index;
the percentage of the P B -B agent in the mixture is expressed as a percentage (%).
Wherein: ctc—co-toxicity coefficient; ati—actual measured virulence index of the mixture; tti—theoretical toxicity index of the mixture.
The co-toxicity coefficient CTC of the compound combination is more than or equal to 120, and the synergistic effect is shown; ctc.ltoreq.80 shows antagonism; 80 < CTC < 120 shows additive effect.
Test results: the combination of the hydroprene and different pyrethroid medicaments shows different combined actions on tomato bemisia tabaci. As shown in table 1, the mass ratio of the dicycloprid to the beta-cypermethrin is 1:2.5-1:2, the synergistic effect is shown, and the additive effect is shown under other proportions. As shown in table 2, the mass ratio of the hydroprene to the deltamethrin is 1:1-2.5: the synergistic effect is shown in the 1 st stage, and the additive effect is shown in the other stages. As can be seen from Table 3, the mixture ratio of the bifenthrin to the iprovalicarb is in the range of 1:5-5:1.
When the composition shows a synergistic effect, the dosage of the active ingredients can be effectively reduced, the generation of drug resistance of tomato bemisia tabaci is slowed down, the environmental pollution is lightened, and the food safety is ensured.
TABLE 1 determination of the combined effects of Dipropisochlamum and beta-cypermethrin on Bemisia tabaci
TABLE 2 determination of the combined action of Dipropisochlamum and deltamethrin on Bemisia tabaci
TABLE 3 determination of the combined effects of Bispyriferyl and bifenthrin on Bemisia tabaci
Example 2 formulation example
Formulation 1:
3.5% of diester-cyanuric chloride suspending agent, which comprises the following components in percentage by weight: 1% of hydroprene, 2.5% of beta-cypermethrin, 4% of sodium lignin sulfonate, 3% of calcium dodecyl benzene sulfonate, 0.2% of SP-2702%, 0.2% of xanthan gum, 0.5% of sodium benzoate, 2% of ethylene glycol, 0.5% of organosilicon, 3% of white carbon black and deionized water which make up 100%.
Formulation 2:
6% bis-ester-cyanuric chloride suspending agent
2% Of hydroprene, 4% of beta-cypermethrin, 3% of sodium lignin sulfonate, 4% of calcium dodecyl benzene sulfonate, 0.1% of SP-2700%, 0.5% of xanthan gum, 2.5% of sodium benzoate, 0.5% of ethylene glycol, 2% of organic silicon, and 100% of white carbon black and deionized water.
Formulation 3:
4% diester bromocyanides suspending agent
2% Of dicycloprid, 2% of deltamethrin, 4% of calcium dodecyl benzene sulfonate, 3% of nekal, 3% of SP-2800%, 3% of magnesium aluminum silicate, 1% of sodium benzoate, 3% of glycol, 0.5% of organosilicon, 4% of white carbon black and 100% of deionized water.
Formulation 4:
4% diester bromocyanides suspending agent
2.5% Of dicycloprid, 1.5% of deltamethrin, 2% of calcium dodecyl benzene sulfonate, 4% of nekal, 2% of SP-2800, 2% of magnesium aluminum silicate, 0.8% of sodium benzoate, 2% of ethylene glycol, 0.3% of organosilicon, 3% of white carbon black and deionized water which are added to make up 100%.
Formulation 5:
3% of a diester-cyanuric chloride dispersible agent, comprising the following components in percentage by weight:
1% of hydroprene, 2% of high-efficiency cypermethrin, 4% of tween 80, 1601% of agricultural emulsion, 3% of synergist methyl oleate, 2% of glycerol, 10% of ethanol and 100% of soybean oil.
Formulation 6:
the 4% diester-bromothalonil dispersible agent comprises the following components in percentage by weight:
2% of hydroprene, 2% of deltamethrin, 4% of tween 80, 3% of agricultural emulsion 1601, 3% of synergist methyl oleate, 2% of glycerol, 15% of ethanol and 100% of soybean oil.
Comparative formulation 1 (without synergist)
3% Of a diester-cyanuric chloride dispersible agent, comprising the following components in percentage by weight:
1% of dicycloprid, 2% of high-efficiency cypermethrin, 4% of tween 80, 1601 of agricultural emulsion, 2% of glycerol, 10% of ethanol and 100% of soybean oil.
Comparative formulation 2 (without synergist)
The 4% diester-bromothalonil dispersible agent comprises the following components in percentage by weight:
2% of dicycloprid, 2% of deltamethrin, 4% of tween 80, 3% of agricultural emulsion 1601, 2% of glycerol, 15% of ethanol and 100% of soybean oil.
Example 3 field control of tomato bemisia tabaci by combination of Dipropisochlor and pyrethrin
Testing crop pests: tomato bemisia tabaci
The testing method comprises the following steps: the cell area is 45m 2, the random block arrangement is repeated for 4 times. The spray is used for uniformly spraying all parts of the whole tomato plant, and the dosage of the liquid medicine is 750kg/hm 2. In order to reduce human error, the humidity of the control area is kept consistent with that of the control area, and the control area is sprayed with equal amount of clean water when spraying the pesticide. A 5-point sampling method is adopted for each cell in the test, and 10 tomatoes are sampled in each cell; the number of insects was investigated before the drug, and the number of residual insects was investigated 14 days after the drug. The following formula data processing and analysis are adopted:
Rate of reduction of insect population = (pre-drug insect population base-post-drug number of living insects)/pre-drug insect population base x 100%
Control effect = (rate of reduction of insect population in treatment area-rate of reduction of insect population in control area)/(rate of reduction of insect population in control area 100%
Test results: as can be seen from Table 4, the suspending agent and the dispersible agent prepared by the invention have excellent control effect on tomato bemisia tabaci. In addition, the addition of the synergist methyl oleate into the dispersible agent can improve the pest control effect of the preparation: compared with the comparative preparation 1, the preparation 5 has the obvious difference that the methyl oleate is added into the preparation 5 to promote the prevention effect of the 3% diester-cyanuric chloride dispersible agent to be obviously improved. Compared with the comparative preparation 2, the preparation 6 has the advantages that the methyl oleate is added to promote the prevention effect of the 4% diester-bromothalonil dispersible agent, but no obvious difference exists, and the specific reasons are to be further studied.
Table 4 field efficacy test of the formulations against tomato bemisia tabaci
Example 4 field control of wheat aphid with the combination of Dipropisochlor and pyrethroid
Testing crop pests: wheat aphid
The testing method comprises the following steps: the cell area is 50m 2, the random block arrangement is repeated for 4 times. The liquid medicine is uniformly sprayed on all parts of wheat, mainly wheat ears and upper leaves, and the dosage of the liquid medicine is 750kg/hm 2. The control area was sprayed with an equal amount of clear water. A 5-point sampling method is adopted for each cell in the test, and 20 wheat plants are sampled in each cell; the number of insects was investigated before the drug, and the number of remaining insects was investigated 7 days after the drug. The following formula data processing and analysis are adopted:
Rate of reduction of insect population = (pre-drug insect population base-post-drug number of living insects)/pre-drug insect population base x 100%
Control effect = (rate of reduction of insect population in treatment area-rate of reduction of insect population in control area)/(rate of reduction of insect population in control area 100%
Test results: as shown in Table 5, the dispersible agent prepared by the invention has excellent control effect on wheat aphids. In addition, the synergistic agent methyl oleate can be added into the dispersion liquid to improve the control effect of the preparation on wheat aphids: compared with the comparative preparation 1, the preparation 5 has the obvious difference that the methyl oleate is added into the preparation 5 to promote the prevention effect of the 3% diester-cyanuric chloride dispersible agent to be obviously improved. Compared with the comparative preparation 2, the preparation 6 has the advantages that the methyl oleate is added into the preparation 5 to promote the prevention effect improvement of 4% of diester-bromocyanides dispersible agent, but no obvious difference exists; the specific reasons are to be further investigated.
Table 5 field efficacy test of the formulations against wheat aphids
Finally, it should be noted that: the above embodiments are only for illustrating the technical solution of the present invention, and not for limiting the same.
Claims (4)
1. Use of a pesticide composition for controlling bemisia tabaci, characterized in that the pesticide composition comprises a triclopyr and a pyrethroid pesticide; the pyrethroid pesticide is beta-cypermethrin, and the weight ratio of the beta-propiconazole to the pyrethroid pesticide is 1 (2-2.5).
2. Use of a pesticide composition for controlling bemisia tabaci, characterized in that the pesticide composition comprises a triclopyr and a pyrethroid pesticide; the pyrethroid pesticide is deltamethrin, and the weight ratio of the difenoconazole to the pyrethroid pesticide is (1-2.5): 1.
3. The use according to claim 1, characterized in that the pesticide composition is a 3% diester-cyanuric chloride dispersible formulation comprising the following components in weight percentage: 1% of hydroprene, 2% of high-efficiency cypermethrin, 4% of tween 80, 1601% of agricultural emulsion, 3% of synergist methyl oleate, 2% of glycerol, 10% of ethanol and 100% of soybean oil.
4. The use according to claim 2, characterized in that the pesticide composition is a 4% diester-bromothalonil dispersible formulation comprising the following components in weight percentage: 2% of hydroprene, 2% of deltamethrin, 4% of tween 80, 3% of agricultural emulsion 1601, 3% of synergist methyl oleate, 2% of glycerol, 15% of ethanol and 100% of soybean oil.
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
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CN101626687A (en) * | 2007-03-08 | 2010-01-13 | 明治制果株式会社 | Pest control composition |
CN102905528A (en) * | 2010-05-28 | 2013-01-30 | 巴斯夫欧洲公司 | Pesticidal mixtures |
CN106106500A (en) * | 2016-06-24 | 2016-11-16 | 江苏省绿盾植保农药实验有限公司 | A kind of containing double third ring worm esters and the composite insecticide of ethofenprox and application |
CN106857640A (en) * | 2017-03-20 | 2017-06-20 | 陕西上格之路生物科学有限公司 | A kind of Pesticidal combination containing double third ring worm esters |
CN111669972A (en) * | 2018-01-29 | 2020-09-15 | 巴斯夫农业公司 | Novel agrochemical formulations |
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Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
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CN101626687A (en) * | 2007-03-08 | 2010-01-13 | 明治制果株式会社 | Pest control composition |
CN102905528A (en) * | 2010-05-28 | 2013-01-30 | 巴斯夫欧洲公司 | Pesticidal mixtures |
CN106106500A (en) * | 2016-06-24 | 2016-11-16 | 江苏省绿盾植保农药实验有限公司 | A kind of containing double third ring worm esters and the composite insecticide of ethofenprox and application |
CN106857640A (en) * | 2017-03-20 | 2017-06-20 | 陕西上格之路生物科学有限公司 | A kind of Pesticidal combination containing double third ring worm esters |
CN111669972A (en) * | 2018-01-29 | 2020-09-15 | 巴斯夫农业公司 | Novel agrochemical formulations |
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