CN109315398A - A kind of pheromones analogue improving Xestia c nigrum gyplure attractant effect - Google Patents

A kind of pheromones analogue improving Xestia c nigrum gyplure attractant effect Download PDF

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Publication number
CN109315398A
CN109315398A CN201710644105.4A CN201710644105A CN109315398A CN 109315398 A CN109315398 A CN 109315398A CN 201710644105 A CN201710644105 A CN 201710644105A CN 109315398 A CN109315398 A CN 109315398A
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CN
China
Prior art keywords
xestia
nigrum
pheromones
cis
acetic acid
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Pending
Application number
CN201710644105.4A
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Chinese (zh)
Inventor
梅向东
翁爱珍
王安佳
张智
张云慧
王留洋
折冬梅
宁君
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Institute of Plant Protection of Chinese Academy of Agricultural Sciences
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Institute of Plant Protection of Chinese Academy of Agricultural Sciences
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Priority to CN201710644105.4A priority Critical patent/CN109315398A/en
Publication of CN109315398A publication Critical patent/CN109315398A/en
Pending legal-status Critical Current

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    • 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
    • A01N37/02Saturated carboxylic acids or thio analogues thereof; Derivatives thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01MCATCHING, TRAPPING OR SCARING OF ANIMALS; APPARATUS FOR THE DESTRUCTION OF NOXIOUS ANIMALS OR NOXIOUS PLANTS
    • A01M1/00Stationary means for catching or killing insects
    • A01M1/02Stationary means for catching or killing insects with devices or substances, e.g. food, pheronones attracting the insects
    • 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
    • A01N31/00Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
    • A01N31/02Acyclic compounds
    • 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
    • A01N35/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
    • A01N35/02Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing aliphatically bound aldehyde or keto groups, or thio analogues thereof; Derivatives thereof, e.g. acetals

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

Abstract

The invention discloses a kind of pheromones analogues for improving Xestia c nigrum gyplure attractant effect.The pheromones analogue is alcohol, aldehyde or the esters along (anti-) formula, the number of carbon is N, position of double bond is 2n+1 or without double bond, the Xestia c nigrum sex attractant are as follows: cis- 7- tetradecene acetic acid esters, cis- 5- tetradecene acetic acid esters and trans- 5- tetradecene acetic acid esters, mass ratio 90:8:2.Pheromones analogue of the invention can more effectively trap and kill Xestia c nigrum male worm, to reduce female male worm collision probability, Insect pest suppression reduces breeding potential, the extinction of pest population gradually be controlled, to achieve the purpose that pest control.Not only dosage is few and environmentally friendly by the present invention, can also accurately be applied to detecting and reporting pest information, Insect pest suppression, mass trapping, be of great significance for the comprehensive treatment of Xestia c nigrum.

Description

A kind of pheromones analogue improving Xestia c nigrum gyplure attractant effect
Technical field
The invention belongs to technical field of biological control, and in particular to a kind of to improve Xestia c nigrum gyplure attractant effect Pheromones analogue.
Background technique
Xestia c nigrum belongs to Lepidoptera Noctuidae, is that root important pests are cut on main agricultural, grassland.Larva tool Seemingly-dead property, hides by day and comes out at night and concealment is stronger.Be distributed in all over the world, the feeding habits such as tobacco, tomato, wild cabbage, grape that can cause harm compared with Extensively, mainly cause harm 100 various plants such as cereal crops, cotton, tobacco, vegetables, medicinal plant in China, with the various plants that cause harm Seedling and it is famous, distribution geographical location it is throughout the country.Currently, the method prevented and treated it mainly sprays chemical agent, lures Kill adult.Agro-chemicals control Xestia c nigrum, which is used for a long time, may make pest develop drug resistance, kill natural enemy, polluting environment With destroy the ecosystem and control efficiency it is unstable, do not have still fundamentally to control its effective ways.
In nature, Xestia c nigrum female adult pest can discharge sex pheromone after sexal maturity to lure male worm, make its to Source orientation flight is discharged, and is mated with the female adult pest of release sex pheromone to produce offspring.Xestia c nigrum sex pheromone is main Ingredient is cis- 7- tetradecene acetic acid esters, and cis- 5- tetradecene acetic acid esters and trans- 5- tetradecene acetic acid esters, weight ratio are 90:8:2.The application study of insect infochemical is increasingly paid attention to both at home and abroad, the infochemical of more pests is not Disconnected identified, synthesis and Field information.Although sex pheromone has many advantages, such as that selectivity is strong, micro efficient, environmentally friendly, Male of the same race can only be trapped and killed, better effects could be obtained for the type of single virgin queen, it is close in wild female moth population It is ineffective when spending higher.
Summary of the invention
The purpose of the present invention is to provide a kind of pheromones structure for improving Xestia c nigrum gyplure attractant effect is similar Object.
A kind of pheromones analogue improving Xestia c nigrum gyplure attractant effect, the pheromones structure are similar Object is alcohol, aldehyde or the esters along (anti-) formula, and the number of carbon is N (N is the positive integer more than or equal to 12), and position of double bond is 2n+1 (n For any positive integer less than N) or without double bond.
The gyplure group is divided into the sex pheromone of Xestia c nigrum: cis- 7- tetradecene acetic acid esters, cis- 5- 14 Carbene acetic acid esters and trans- 5- tetradecene acetic acid esters.
Preferably, the weight ratio of the Xestia c nigrum gyplure and pheromones analogue is 1:(0.05-10), institute Stating pheromones analogue is alcohol, aldehyde or the esters along (anti-) formula, and it is 3~8 or unparalleled that carbon number, which is 12~18 position of double bond, Key.
The pheromones analogue is selected from cis- 3- dodecylene yl acetate, and cis- 9- tetradecene acetic acid esters is cis- 14 carbon acetic acid esters of 11-, cis- 13- hexadecene acetic acid esters, cis- 7- hexadecenol, cis- 5- octadecene aldehyde, trans- 5- ten Four carbene alcohol, trans- 7- hexadecene acetic acid esters, one of 14 carbon acetic acid esters or more than one.
The preparation method of the lure of above-mentioned pheromones analogue carries out in accordance with the following steps:
(1) cylindrical indent rubber stopper, high 0.5~2cm, bottom 0.5~2cm of diameter are chosen;
(2) pheromones analogue described in claim 1 is diluted to concentration with just oneself burning is 0.01~1 μ g/ μ L's Solution is drawn 50~200 μ L and is added to the recess portion of rubber stopper;
(3) natural evaporation is complete to n-hexane volatilization, and it is spare to be placed in -20 DEG C of refrigerators.
Purposes of the above-mentioned pheromones analogue in terms of Xestia c nigrum biological control.
It compared with prior art, can be with the invention has the following beneficial effects: pheromones analogue 1) of the invention Mass trapping Xestia c nigrum male worm kills to physics;2) production of this pheromones analogue is simple and raw material is easy to get;3) This pheromones analogue applies to field mass control pest, with few, the environmentally friendly and laborsaving feature of dosage.The present invention Pheromones analogue by mass trapping, reduce breeding potential, the extinction of pest population gradually controlled, to reach prevention and treatment The purpose of pest can accurately be applied to detecting and reporting pest information, pest quarantine, mass trapping, reach the reason of comprehensive treatment Xestia c nigrum Think effect.
Detailed description of the invention
Fig. 1 is cis- 3- dodecenyl succinic acetic acid esters chemical structural formula schematic diagram.
Fig. 2 is cis- 9- tetradecene acetic acid esters chemical structural formula schematic diagram.
Fig. 3 is cis- 14 carbon acetic acid esters chemical structural formula schematic diagram of 11-.
Fig. 4 is cis- 13- hexadecene acetic acid esters chemical structural formula schematic diagram.
Fig. 5 is cis- 7- hexadecenol chemical structural formula schematic diagram.
Fig. 6 is cis- 5- octadecene aldehyde chemical structural formula schematic diagram.
Fig. 7 is trans- 5- tetradecene alcohol chemical structural formula schematic diagram
Fig. 8 is trans- 7- hexadecene acetic acid esters chemical structural formula schematic diagram
Fig. 9 is 14 carbon acetic acid esters chemical structural formula schematic diagrames.
Specific embodiment
With reference to the accompanying drawing, specific embodiments of the present invention will be described in detail, it is to be understood that guarantor of the invention Shield range is not limited by the specific implementation.
The test of 1 field biological activity determination of embodiment
Lure preparation:
(1) lure carrier is using cylindrical green indent rubber stopper, high 1cm, bottom diameter 1cm.
(2) by the cis- 7- tetradecene acetic acid esters of Xestia c nigrum pheromone component, cis- 5- tetradecene acetic acid esters and trans- 5- tetradecene acetic acid esters is mixed with the mass ratio of 90:8:2, is diluted to the solution that concentration is 1 μ g/ μ L with n-hexane.
(3) 100 μ L (1 μ g/ μ L) above-mentioned Xestia c nigrum pheromones solution is drawn to be added to Rubber end bottom, eight words it is old Brave pheromones solution can penetrate into inside rubber with solvent (n-hexane).After solvent (n-hexane) volatilization, the eight of 100 μ g are obtained Word cutworm pheromones.
(4) by cis- 3- dodecylene yl acetate, cis- 9- tetradecene acetic acid esters, cis- 14 carbon acetic acid esters of 11- is cis- 13- hexadecene acetic acid esters, cis- 7- hexadecenol, cis- 5- octadecene aldehyde, trans- 5- tetradecene alcohol, trans- 16 carbon of 7- Alkene acetic acid esters, 14 carbon acetic acid esters are diluted with n-hexane respectively, and concentration is 0.1 μ g/ μ L.The structural formula of above-mentioned eight compounds is such as Shown in Figure of description (Fig. 1-9).
(5) the step of drawing 50 μ L (0.1 μ g/ μ L) (4) solution is added to step (3) oneself Xestia c nigrum for preparing and lures To which mixing lure be made in core.Therefore, in Xestia c nigrum lure, Xestia c nigrum sex pheromone is similar with pheromones structure The mass ratio of object is 100:5.It is spare that lure is placed in -20 DEG C of refrigerators before test.
The plot for selecting Xestia c nigrum hazard ratio more serious, trapper are the universal trapper of moth class, and trapper is put 20cm or so above crop is set, the average headway between trapper is in 10m or more.Above-mentioned each mixing lure processing is respectively provided with 5 repetitions.As control Xestia c nigrum sex pheromone (cis- 7- tetradecene acetic acid esters: cis- 5- tetradecene acetic acid esters: Trans- 5- tetradecene acetic acid esters=90:8:2) lure and space management be respectively 5 repetitions.
Recording method:
The trapping quantity for recording primary each trapper for every two days, polypide is pulled out and is handed at random between rear different processing group Change place is observed continuously 30 days with eliminating position effect bring test error.Test result is as shown in table 1.
Trapping experiments result of the 1 pheromones analogue of table to Xestia c nigrum
As seen from the results in Table 1, pheromones analogue of the invention has preferable control efficiency to Xestia c nigrum.Contain The trapping amount of the Xestia c nigrum mixing gyplure of pheromones analogue is above the trapping of Xestia c nigrum sex pheromone Amount illustrates that this few parapheromone analogue has certain attractive activity to Xestia c nigrum, and wherein Xestia c nigrum is believed Breath element: cis- 5- octadecene aldehyde: cis- 7- hexadecenol: 14 carbon acetic acid esters: cis- 13- hexadecene acetic acid esters, mass ratio For 100:2:0.5:0.5:2, the mixing gyplure attractive activity highest of this formula rate.
It also can be seen that by table 1, the trap effect of pheromones analogue cis and trans is different, trans- pheromones structure The attractant effect of analog is weaker than the attractive activity of cis- pheromones analogue.The position of double bond, the number of carbon and information The different formulations ratio of plain analogue has different degrees of influence to Xestia c nigrum attractive activity.
The pheromones analogue preparation of Xestia c nigrum provided by the invention is simple, and raw material is easy to get;With very strong Trapping capability, stability is good, and the lasting period is long, and control efficiency can maintain 30 days or more;Specificity is strong, Xestia c nigrum will not be made to produce Raw resistance;It is environmental-friendly to person poultry harmless;Resistance is strong, easy to use.The present invention can accurately be applied to detecting and reporting pest information, a large amount of Trapping, is of great significance for comprehensive treatment Xestia c nigrum.
Disclosed above is only specific embodiments of the present invention, and still, the present invention is not limited to this, any this field What technical staff can think variation should all fall into protection scope of the present invention.

Claims (5)

1. a kind of pheromones analogue for improving Xestia c nigrum gyplure attractant effect, which is characterized in that the information Plain analogue is alcohol, aldehyde or the esters of cis or trans, and the number of carbon is N, and position of double bond is 2n+1 or without double bond;
The N is the positive integer more than or equal to 12;The n is any positive integer less than N.
2. improving the pheromones analogue of Xestia c nigrum gyplure attractant effect, feature according to claim 1 It is, the Xestia c nigrum gyplure are as follows: cis- 7- tetradecene acetic acid esters, cis- 5- tetradecene acetic acid esters and trans- 5- Tetradecene acetic acid esters, mass ratio 90:8:2.
3. improving the pheromones analogue of Xestia c nigrum gyplure attractant effect, feature according to claim 1 It is, the pheromones analogue is selected from cis- 3- dodecylene yl acetate, cis- 9- tetradecene acetic acid esters, cis- 11- 14 carbon acetic acid esters, cis- 13- hexadecene acetic acid esters, cis- 7- hexadecenol, cis- 5- octadecene aldehyde, trans- 14 carbon of 5- Enol, trans- 7- hexadecene acetic acid esters, one of 14 carbon acetic acid esters or more than one.
4. the system of the lure of the pheromones analogue described in claim 1 for improving Xestia c nigrum gyplure attractant effect Preparation Method, which is characterized in that carry out in accordance with the following steps:
(1) cylindrical indent rubber stopper, high 0.5 ~ 2 cm, 0.5 ~ 2 cm of bottom diameter are chosen;
(2) just oneself burning of pheromones analogue described in claim 1 is diluted to the solution that concentration is 0.01 ~ 1 μ g/ μ L, 50 ~ 200 μ L are drawn to be added to the recess portion of rubber stopper;
(3) natural evaporation is complete to n-hexane volatilization, and it is spare to be placed in -20 DEG C of refrigerators.
5. purposes of the pheromones analogue described in claim 1 in terms of Xestia c nigrum biological control.
CN201710644105.4A 2017-07-31 2017-07-31 A kind of pheromones analogue improving Xestia c nigrum gyplure attractant effect Pending CN109315398A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115812712A (en) * 2022-12-06 2023-03-21 黑龙江省森林保护研究所 Sex attractant analogue for preventing and controlling moths in pine tips of camphor trees

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Publication number Priority date Publication date Assignee Title
CN115812712A (en) * 2022-12-06 2023-03-21 黑龙江省森林保护研究所 Sex attractant analogue for preventing and controlling moths in pine tips of camphor trees
CN115812712B (en) * 2022-12-06 2024-05-28 黑龙江省森林保护研究所 Sex attractant analogue for preventing and controlling pinus sylvestris

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