CN118044513A - Botanical insecticidal composition for preventing and controlling peach aphids of peach trees - Google Patents
Botanical insecticidal composition for preventing and controlling peach aphids of peach trees Download PDFInfo
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- peach
- limonene
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- 241000256593 Brachycaudus schwartzi Species 0.000 title claims abstract description 28
- 230000000749 insecticidal effect Effects 0.000 title claims abstract description 18
- 244000144730 Amygdalus persica Species 0.000 title claims abstract description 17
- 235000006040 Prunus persica var persica Nutrition 0.000 title claims abstract description 17
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 claims abstract description 64
- -1 pentadecene phenolic acid Chemical class 0.000 claims abstract description 18
- HOGWBMWOBRRKCD-BUHFOSPRSA-N trans-2-pentadecenoic acid Chemical compound CCCCCCCCCCCC\C=C\C(O)=O HOGWBMWOBRRKCD-BUHFOSPRSA-N 0.000 claims abstract description 11
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
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- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
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- 239000004359 castor oil Substances 0.000 description 2
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- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000010413 mother solution Substances 0.000 description 2
- 229930014626 natural product Natural products 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
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- 241000233866 Fungi Species 0.000 description 1
- 239000005906 Imidacloprid Substances 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
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- 102000003992 Peroxidases Human genes 0.000 description 1
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- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
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- 230000036541 health Effects 0.000 description 1
- 238000005286 illumination Methods 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
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
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- 238000005259 measurement Methods 0.000 description 1
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- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229930003647 monocyclic monoterpene Natural products 0.000 description 1
- 150000002767 monocyclic monoterpene derivatives Chemical class 0.000 description 1
- 210000003097 mucus Anatomy 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 108040007629 peroxidase activity proteins Proteins 0.000 description 1
- 230000003285 pharmacodynamic effect Effects 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
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- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 238000000611 regression analysis Methods 0.000 description 1
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- 210000002784 stomach Anatomy 0.000 description 1
- 231100000820 toxicity test Toxicity 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N37/00—Biocides, 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
- A01N37/36—Biocides, 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 singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—Biocides, 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 singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
- A01N37/40—Biocides, 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 singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N27/00—Biocides, pest repellants or attractants, or plant growth regulators containing hydrocarbons
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P7/00—Arthropodicides
- A01P7/04—Insecticides
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- Life Sciences & Earth Sciences (AREA)
- Plant Pathology (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Chemical & Material Sciences (AREA)
- Insects & Arthropods (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
The invention discloses a botanical insecticidal composition for preventing and controlling peach aphids of peach trees, and belongs to the technical field of pesticides. The plant-derived insecticidal composition provided by the invention comprises the active ingredients of d-limonene and pentadecenoic acid. The mass ratio of the d-limonene to the pentadecene phenolic acid is 1:9-5:5. The invention is used for preventing and controlling peach aphids of peach trees after the d-limonene and pentadecene phenolic acid are compounded, and shows a synergistic effect.
Description
Technical Field
The invention belongs to the technical field of pesticides, and particularly relates to a botanical insecticidal composition for preventing and controlling peach aphids.
Background
The green peach aphids are also called green peach aphids and myzus persicae. Is widely distributed and occurs all over the country. The plant is mainly a peach tree, and also is a plurality of fruit trees such as apricot, plum, cherry, pear, orange and the like and a plurality of plants of cruciferae. The peach aphid is one of main pests of peach trees and also transmits various viruses. The growth of young shoots and leaf backs of adults and nymphs are taken as harm, the damaged leaves shrink and curl, the growth of the young shoots is seriously influenced, fungi are bred in the later period of excreted honey-like mucus, mildew is formed, and the appearance quality of fruits is influenced.
The prevention and control of the green peach aphids in agricultural production mainly depends on chemical pesticides. The chemical agent can kill natural enemies of the green peach aphids, destroy ecological balance, seriously weaken natural control capability in fields and easily cause rampant of the green peach aphids while preventing and controlling the green peach aphids. The large amount of chemical agents causes the peach aphids to generate drug resistance, which makes the peach aphids difficult to control. Along with the improvement of people's health, food safety and environmental awareness, the development of pesticides is also shifted towards high efficiency, safety and low residue. There is a start to find highly active substances from natural products instead of traditional chemical pesticides. The reasonable mixing can not only improve the control effect of pesticides and reduce the dosage, but also effectively delay the development of the drug resistance of plant diseases and insect pests. Therefore, development of efficient, safe and low-residue natural product active substances for preventing and controlling the green peach aphids and a compound composition thereof are urgently needed.
D-limonene is a monocyclic monoterpene, exists in a large amount in citrus plants such as oranges, kumquats, lemons and grapefruits, and has been reported to be used for preventing and controlling plant diseases and insect pests such as bemisia tabaci, red spiders, anthracnose and powdery mildew.
Pentadecene phenolic acid is an active substance obtained from ginkgo fruit extract. The ginkgo nut is extracted to have insecticidal activity, and the tanning of proteins in the insect epidermis is influenced by inhibiting the activity of the aminopeptidase of the insect epidermis, so that the hardening and darkening of the insect epidermis are interfered; by inhibiting the activities of peroxidase, hydrogenoxidase, etc., the metabolism and development of insects are disturbed, and the insects are killed. The action mode is contact killing and stomach poisoning, and can effectively control the occurrence of aphids.
At present, reports of d-limonene and pentadecenoic acid compound used for preventing and controlling peach aphids of peach trees are not yet seen. Therefore, the development of an agricultural composition with d-limonene and pentadecene phenylphenol acid as active ingredients can improve the pesticide effect and reduce the pesticide dosage, and has important significance.
Disclosure of Invention
Aiming at the defects or shortcomings in the prior art, the invention aims to provide a botanical insecticidal composition for preventing and controlling peach aphids of peach trees.
In order to achieve the above object, the present invention provides the following solutions:
The plant source insecticidal composition for preventing and controlling peach aphids comprises the active ingredients of d-limonene and pentadecenoic acid, wherein the mass ratio of the d-limonene to the pentadecenoic acid is 1:9-5:5.
Further, the mass ratio of d-limonene to pentadecenoic acid is 3:7.
The botanical insecticidal composition of the invention can be prepared into a soluble agent.
The soluble agent comprises an active ingredient, a solvent and a surfactant, wherein the active ingredient accounts for 5-30% of the total mass of the composition, the surfactant accounts for 5-15% of the total mass of the composition, and the balance is the solvent.
The surfactant is one or more of castor oil polyoxyethylene ether, sodium dodecyl sulfate, calcium dodecyl benzene sulfonate, fatty acid polyoxyethylene ether, styrylphenol polyoxyethylene ether, nonylphenol polyoxyethylene ether, fatty acid polyoxyethylene ester and polyoxyethylene fatty alcohol ether.
The solvent is one or more selected from cyclohexanone, dimethyl sulfoxide, N-methyl pyrrolidone, N-octyl pyrrolidone, N-lauryl pyrrolidone, alpha-pyrrolidone, gamma-butyrolactone, propylene glycol, diethylene glycol, isobutanol, soybean oil and the like.
The botanical insecticidal composition is used for preventing and controlling peach aphids of peach trees.
The invention has the beneficial effects that:
The botanical insecticidal composition disclosed by the invention has the obvious synergistic effect on peach aphids by compounding d-limonene and pentadecenoic acid in a specific ratio. Compared with single use of d-limonene and pentadecenoic acid, the botanical insecticidal composition disclosed by the invention has more excellent prevention effect on peach aphids, reduces the dosage of the agent and reduces the cost. Meanwhile, the d-limonene and pentadecenyl phenolic acid belong to plant-source pesticides, are easy to degrade, have low residues, are safer to agricultural products and are more environment-friendly.
Detailed Description
The following describes the technical aspects of the present invention with reference to examples, but the present invention is not limited to the following examples. The experimental methods and the detection methods in each embodiment are conventional methods unless otherwise specified; the reagents and materials are commercially available unless otherwise specified.
Example 1
Indoor toxicity test of d-limonene and pentadecylphenol acid compounding
Testing insects: and (3) collecting the imago of the peach aphids from peach plants in the peach orchard in Liquan county of Shaanxi province, feeding the imago of the peach aphids indoors for 1-2 generations, and picking the imago of the wing-free peach aphids for indoor toxicity measurement.
Test agent:
93% d-limonene original drug (CAS: 5989-27-5): qingdao Richeng source crop nutrient Limited
Pentadecene phenol acid standard 98% (CAS: 22910-60-7): chengDude Biotechnology Co.
Dissolving the reagent d-limonene with acetone, dissolving pentadecylphenol acid with methanol, diluting with 0.1% Tween-80 aqueous solution, preparing single-dose mother solution and mixed-dose mother solution, and setting 5 mass concentration gradients for the single-dose and mixed-dose according to an equal ratio method.
The test method comprises the following steps: the blade spraying method is adopted. And picking the wing-free green peach aphids with the same size onto the leaves of the peach tree by using a soft brush, wherein each leaf is 30. The test liquid is sprayed onto the insect-carrying leaves by a small sprayer, and the whole leaves are sprayed with the test liquid until the whole leaves are wet, the process is repeated for 3 times, and clear water control is additionally arranged. The treated insect-carrying leaves are dried by using absorbent paper and then placed into a 9cm culture dish, and the culture is carried out in an illumination incubator under the conditions of temperature (25+/-1) DEG C, relative humidity of 70% -80% and sunlight for 16 hours. Mortality was checked for 24h and the body response was taken as mortality standard with the writing brush tip.
Data analysis: regression analysis is carried out according to the logarithmic value of each medicament concentration and the corresponding mortality probability value, LC 50 of each medicament is calculated, interaction of the mixture is evaluated according to the Wadley method, wherein SR=0.5-1.5, and then the two medicaments are compounded to have additive effect; SR is less than or equal to 0.5, and antagonism is achieved; SR is more than or equal to 1.5, and the synergy is achieved. The test results of the compounding of d-limonene and pentadecylphenol acid are shown in Table 1.
LC 50 (theoretical) = (a+b)/(a/LC 50a+b/LC50 b);
Sr=lc 50 (theoretical value)/LC 50 (actual value);
wherein SR is the synergistic coefficient, and a and b are the percentage contents of each component in the mixture.
TABLE 1 results of indoor Activity of limonene and pentadecenoic acid Complex against peach aphid
From Table 1, it is known that the synergy coefficient of d-limonene and pentadecenoic acid to peach aphid is greater than 1.5 in the mass ratio of 1:9-5:5, and the synergy effect is particularly remarkable, and especially when the mass ratio is 3:7, the synergy coefficient reaches 5.20.
Example two
D-limonene pentadecenoic phenol acid compound preparation
Example 1
30% D-limonene pentadecene phenylphenol acid soluble
The contents of the following substances are weight percent: 3% of d-limonene, 27% of pentadecene phenolic acid, 12% of castor oil polyoxyethylene ether, 6% of cyclohexanone and 100% of soybean oil. The materials are mixed according to a certain proportion, and after being stirred uniformly, the 30% d-limonene pentadecene phenolic acid soluble agent can be prepared.
Example 2
20% D-limonene pentadecene phenylphenol acid soluble
The contents of the following substances are weight percent: 6% of d-limonene, 14% of pentadecenophenolic acid, 7% of fatty acid polyoxyethylene ether, 3% of sodium dodecyl sulfate, 5% of N-octyl pyrrolidone and 100% of soybean oil. The materials are mixed according to a certain proportion, and after being stirred uniformly, the solution of 20% d-limonene pentadecene phenolic acid can be prepared.
Example 3
10% D-limonene pentadecene phenylphenol acid soluble
The contents of the following substances are weight percent: 5% of d-limonene, 5% of pentadecylphenol acid, 6% of nonylphenol polyoxyethylene ether, 4% of cyclohexanone and 100% of soybean oil. The materials are mixed according to a certain proportion, and after being stirred uniformly, the solution of 10 percent of d-limonene pentadecene phenolic acid can be prepared.
Example III
Field efficacy test for preventing and controlling peach aphids of peach trees
According to the pesticide effect test criterion (I) in agricultural fields: the pesticide can be used for preventing and controlling fruit and vegetable aphid (GB/T17980.9-2000).
Control object: peach aphid of peach tree
Test site: liquan county of Shanxi province
The test method comprises the following steps: the test was carried out in a peach garden where the occurrence of peach aphids was severe. Cell area 20m 2, 4 replicates per treatment, blank control was set. The cells of the test agent, control agent and blank are arranged randomly. The application method is spraying. Spraying and applying the pesticide 1 time in the initial flourishing period of the peach aphid. The number of insect population is investigated before the drug, the control effect is investigated once each 3 days and 7 days after the drug administration, the number of residual living insects is recorded, and the control effect is calculated. The results of the pharmacodynamic tests of the d-limonene and pentadecylphenol acid combination are shown in Table 2.
Table 2 results of field efficacy of d-limonene and pentadecenoic acid Complex on peach aphids
As can be seen from Table 2, the control effect of the compositions of the invention on peach aphids of example 1, example 2 and example 3 is significantly better than that of the single dose of 18% d-limonene soluble solution, 20% pentadecene phenolic acid soluble solution and 70% imidacloprid water dispersible granule of registered control agent, especially 92.8% after the period of example 2 and 7 days, which shows that the composition of the invention has a synergistic effect and is consistent with the indoor combined toxicity result. The botanical insecticidal composition has good prevention effect on peach aphids, reduces the dosage of medicaments and reduces the cost. And (5) observing the field, wherein each treatment agent is safe for peach trees.
The above embodiments are only illustrative of the preferred embodiments of the present invention and are not intended to limit the scope of the present invention, and various modifications and improvements made by those skilled in the art to the technical solutions of the present invention should fall within the protection scope defined by the claims of the present invention without departing from the design spirit of the present invention.
Claims (5)
1. The botanical insecticidal composition for preventing and controlling peach aphids is characterized in that the active ingredients consist of d-limonene and pentadecenoic acid, and the mass ratio of the d-limonene to the pentadecenoic acid is 1:9-5:5.
2. The plant-derived insecticidal composition according to claim 1, wherein the mass ratio of d-limonene to pentadecenoic acid phenol is 3:7.
3. A plant-derived insecticidal composition according to claim 1, wherein said composition is formulated as a soluble formulation.
4. A plant-derived insecticidal composition according to claim 3, comprising an active ingredient, a solvent and a surfactant, wherein the active ingredient comprises 5-30% of the total mass of the composition, the surfactant comprises 5% -15% of the total mass of the composition, and the balance is the solvent.
5. Use of the botanical insecticidal composition as claimed in any one of claims 1 to 4 for controlling peach aphids in peach trees.
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