WO2012015014A1 - Copulation disruption agent for sap-sucking pests - Google Patents

Copulation disruption agent for sap-sucking pests Download PDF

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Publication number
WO2012015014A1
WO2012015014A1 PCT/JP2011/067369 JP2011067369W WO2012015014A1 WO 2012015014 A1 WO2012015014 A1 WO 2012015014A1 JP 2011067369 W JP2011067369 W JP 2011067369W WO 2012015014 A1 WO2012015014 A1 WO 2012015014A1
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Prior art keywords
flonicamid
composition
pest
rice
pests
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PCT/JP2011/067369
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French (fr)
Japanese (ja)
Inventor
潔充 吉田
隆雄 粟津
省吾 渥美
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石原産業株式会社
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Priority to CN201180046967.8A priority Critical patent/CN103140135B/en
Priority to KR1020137005007A priority patent/KR101801427B1/en
Publication of WO2012015014A1 publication Critical patent/WO2012015014A1/en

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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
    • 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
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • 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
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/08Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing solids as carriers or diluents
    • A01N25/10Macromolecular 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
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/12Powders or granules
    • 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
    • A01N43/80Biocides, 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 five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2

Definitions

  • the present invention relates to a copulation disruption agent for sucking pests.
  • N-cyanomethyl-4-trifluoromethyl-3-pyridinecarboxamide (generic name flonicamid) is a compound described as Patent No. 1 in Patent Document 1.
  • Patent Document 2 describes a pesticidal composition containing a pyridine-based compound containing flonicamid and various efficacy enhancing components.
  • Root beetles which are sucking pests that are regarded as the main pests in the field of rice cultivation, have a high growth potential and cause enormous damage to rice.
  • the brown planthopper repeatedly grows over a number of generations until the harvest season, and the main damage is caused by the dryness of rice. “Tsubo withering” refers to the damage that rice dies and / or surrenders due to the sucking damage of the brown planthopper.
  • neonicotinoid insecticides are the mainstream as a control agent for planthoppers, but recently, planthoppers with reduced susceptibility to neonicotinoid insecticides have been seen.
  • a control agent or control method that can replace neonicotinoid insecticides and become a new mainstream.
  • the ecology of the green planthopper is characteristic, and the present inventors conducted research in connection with the characteristic ecology in the control of planthoppers including the green planthopper.
  • Tobiro planta cannot overwinter in areas north of Vietnam.
  • Japan the long-winged adult worms that fly from the lower part of the jet stream from overseas during the rainy season from late June to July are the source.
  • the flying density is considerably lower than that of the overseas flying white smelt, and the parasitic density at the time of flying does not cause a big problem.
  • the copulation behavior disturbing action in the present invention refers to an action of suppressing a series of mating actions in which a female searches for a female by suppressing the action of calling the male by vibration of the abdomen.
  • the present invention relates to a method for controlling sucking pests by causing flonicamid to act on sucking pests, a method for reducing the next generation population of sucking pests, and a method for disturbing the mating behavior of sucking pests.
  • the mating behavior disrupting agent and control method for sucking pests according to the present invention can exhibit a stable and high control effect over a long period of time.
  • the present invention is completely different from the use of flonicamid as a simple pesticide, and has an unexpected effect of reducing the next-generation population of pests.
  • a conventionally used control agent cannot be expected to have a long-lasting residual effect, and therefore it is necessary to treat the spray agent a plurality of times. It is possible to reduce the number of times of agent treatment.
  • Applying the completely unexpected effect of “reducing the next generation of pests” disclosed by the present invention for example, when applied to a seedling box treatment, it is usually desired to control sucking pests over a sufficiently long period of time. The effect is demonstrated.
  • the active ingredient for agricultural chemicals in the present invention is flonicamid.
  • Flonicamid is a common name and its chemical name is N-cyanomethyl-4-trifluoromethyl-3-pyridinecarboxamide. Flonicamid may form a salt.
  • examples of the rice parasitic sucking insects include planthoppers, leafhoppers, and stink bugs.
  • the planthoppers include brown planthoppers, white-spotted planthoppers, and leafhoppers.
  • the leafhoppers include leafhopper leafhoppers and the like, and the stink bugs include akazikakasomika and akahigehosomidorikamikameka.
  • the soup pests preferably include planthoppers and leafhoppers. More preferably, a planthopper is mentioned. More preferred is a brown planthopper.
  • Examples of the sucking pests to be controlled according to the present invention include sucking pests having reduced sensitivity to neonicotinoid insecticides.
  • flonicamid is selected from the group consisting of nonionic surfactants, anionic surfactants, cationic surfactants, amphoteric surfactants, animal and vegetable oils, mineral oils, water-soluble polymers, resins and waxes.
  • at least one efficacy enhancing component can be used in combination.
  • flonicamid can be formulated in various forms such as emulsions, powders, wettable powders, liquids, granules, suspensions and the like by blending with various adjuvants as in the case of conventional agricultural chemical preparations.
  • auxiliary agent include a carrier, a suspending agent, a thickening agent, a stabilizer, a dispersing agent, a wetting agent, a penetrating agent, an antifreezing agent, an antifoaming agent, and the like.
  • Carriers are divided into solid carriers and liquid carriers, and solid carriers include starch, sugar, cellulose powder, cyclodextrin, activated carbon, soybean powder, wheat flour, rice bran powder, wood powder, fish powder, milk powder, and other animal and vegetable powders.
  • Talc kaolin, bentonite, organic bentonite, calcium carbonate, calcium sulfate, sodium bicarbonate, zeolite, diatomaceous earth, white carbon, clay, alumina, silica, sulfur powder, mineral powder such as slaked lime, etc., liquid carrier
  • liquid carrier As: water; alcohols such as ethyl alcohol and ethylene glycol; ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, and isophorone; ethers such as dioxane and tetrahydrofuran; and aliphatic hydrocarbons such as kerosene, kerosene, and liquid paraffin Toluene, xylene, tri Aromatic hydrocarbons such as tilbenzene, tetramethylbenzene, cyclohexane and solvent naphtha; Halogenated hydrocarbons such as chloroform and chlorobenzene; Acid amides such as
  • nitriles such as acetonitrile; sulfur-containing compounds such as dimethyl sulfoxide; N-methyl-2-pyrrolidone and the like.
  • the dispersant include polycarboxylic acid or a salt thereof, lignin sulfonic acid or a salt thereof, and the like.
  • flonicamid can be treated in a nursery box or treated in a paddy field.
  • a seedling box treatment is desirable because a particularly significant effect can be achieved by sucking the soup pest. This is because flonicamid which is an active ingredient of agricultural chemicals having high water solubility can be efficiently taken into the plant body by the action of sucking up the drug from the root of rice by the seedling box treatment.
  • flonicamid can be formulated into various forms as described above, but from the viewpoint that the seedling box treatment is desirable, it is desirable to use a granule for the seedling box treatment.
  • a composition containing flonicamid and a poorly water-soluble resin is used as a granule for treatment of a seedling box suitable for exerting the effects of the present invention.
  • flonicamid and the poorly water-soluble resin are difficult to form a matrix, that is, flonicamid is difficult.
  • the composition characterized by forming the composition taken in by water-soluble resin is mentioned, It mentions in full detail below.
  • the active ingredient flonicamid used in the present invention is known to be a compound having a very high water solubility (water solubility at 20 ° C .: 5200 mg / L). Since chemicals for nursery box treatment need to maintain their efficacy over a long period of time, it is required to control the elution of active ingredients of agricultural chemicals, while a compound with extremely high water solubility such as flonicamid is applied to this usage mode. It has been difficult to do.
  • the composition is an effective embodiment for solving the problems caused by the aqueous solubility of flonicamid.
  • the blending amount is 0.1 to 30% by weight, preferably 0.5 to 25% by weight.
  • the average particle size of flonicamid used in the present invention is 1 to 500 ⁇ m, preferably 1 to 100 ⁇ m, and more preferably 5 to 50 ⁇ m.
  • the poorly water-soluble resin that can be used in the present invention ethylene / vinyl acetate copolymer, ethylene / acrylic acid copolymer, ethylene / veova copolymer, styrene / acrylic acid copolymer, acrylic ester, Acrylic / silicone copolymer, polyethylene oxide, urethane resin, petroleum resin and the like can be mentioned.
  • the poorly water-soluble resin is desirably used as an emulsion, and in particular, an ethylene / acrylic acid copolymer emulsion is desirable.
  • ethylene / acrylic acid copolymer emulsion examples include HYTEC S-3111, HYTEC S-3121, and HYTEC S-3127 (manufactured by Toho Chemical Industry Co., Ltd.). These resin emulsions can be used alone or in combination.
  • the blending amount is 0.1 to 30% by weight, preferably 1 to 15% by weight in terms of solid content.
  • the carrier used in the present invention is not particularly limited, and for example, a carrier such as clay, bentonite, talc, calcium carbonate, gericite, sericite, acid clay, diatomaceous earth, zeolite, perlite, attapulgite and the like can be used. .
  • the blending amount is not particularly limited, but is in the range of 40 to 99.8% by weight, preferably 60 to 98.5% by weight. Since the composition uses a poorly water-soluble resin, it does not fit well with water, and the drug may float after transplantation into Nissan. Therefore, it is desirable to add a wetting agent.
  • the wetting agent include sodium dioctyl sulfosuccinate, sodium alkylbenzene sulfonate, higher alcohol sulfate ester, sodium alkyl naphthalene sulfonate, polyoxyethylene phenyl ether sulfate, polyoxyethylene styryl phenyl ether sulfate, polyoxyethylene alkyl ether, and the like.
  • polyoxyethylene styryl phenyl ether sulfate is used.
  • wetting agents can be used alone or in combination.
  • the blending amount is not particularly limited, but is 0.01 to 10% by weight, preferably 0.1 to 5% by weight.
  • the composition is a granulation method usually used in the production of agricultural chemicals, for example, extrusion granulation method, tumbling granulation method, tumbling fluidized granulation method, fluidized bed granulation method, compression granulation method, stirring and granulation method. It can be prepared by a granulation method, a coating granulation method, a tableting method or the like.
  • an elution control agent such as paraffin can be added to the composition to further control the elution rate as desired.
  • composition in addition to the components described above, as an optional component, for example, the purpose of stably maintaining the pesticidal active ingredient in the pesticidal formulation of the present invention and / or the purpose of improving the granulation property when granulating
  • a surfactant, an auxiliary agent and the like can be contained as necessary.
  • agrochemical components other than flonicamid such as fungicides, insecticides, acaricides, nematicides, antiviral agents, attractants, herbicides, plant growth regulators, etc. Can be used in combination, and in this case, a more excellent effect may be exhibited. For example, it is possible to improve the application range, the timing of chemical treatment, the control activity, and the like in a preferable direction.
  • Flonicamid and the other active ingredient compounds of other agricultural chemicals may be prepared separately and mixed at the time of spraying, or both may be used together. For example, when preparing the composition, it can be formulated together with flonicamid and other agrochemical ingredients.
  • the present invention includes a case where the active ingredients are mixed and applied in this way.
  • an insecticidal compound that is, an insecticidal compound (generic name; including some pending applications or test codes)
  • an insecticidal compound for example, profenofos, dichlorvos, fenamiphos, fenitrothion, EPN, diazinon, chlorpyrifos, chlorpyrifos-methyl, acephatethio, prothiophos , Fosthiazate, cadusafos, dislufoton, isoxathion, isofenphos, ethion, etrimfos, quinalphos, dimethylvinphos, dimethoate (dimethoate) dimethoate), sulprofos, Thiometon, bamidothion, pyraclofos, pyridaphenthion, pirimiphos-methyl, propaphos, phosalone,
  • Bacillus thuringienses aizawai, Bacillus thuringienses kurstaki, Bacillus thuringienses israelensis, Bacillus thuringienses japonensis, Bacillus thuringienses tenebrionis, crystalline protein toxins produced by Bacillus thuringienses, entomopathogenic fungi, nematopathogenic fungi, etc.
  • Microbial pesticides such as avermectin, emamectin benzoate, milbemectin, milbemycin, spinosad, ivermectin, lepimectin, DE-175, abamectin ), Antibiotics such as emamectin, spinetoram and semi-synthetic antibiotics; natural products such as azadirachtin and rotenone; repellents such as deet; etc. And mixed use It is also possible to.
  • a bactericidal agent that is, a bactericidal compound (generic name; including partial application, or Japan Plant Protection Association test code), for example, mepanipyrim, pyrimethanil (pyrimethanil) ), Anilinopyrimidine compounds such as cyprodinil, ferimzone; Tria such as 5-chloro-7- (4-methylpiperidin-1-yl) -6- (2,4,6-trifluorophenyl) [1,2,4] triazolo [1,5-a] pyrimidine Zolopyrimidine compounds; Pyridinamine compounds such as fluazinam; Triadimefon, bitertanol, triflumizole, etaconazole, propiconazole, penconazole, flusilazole, microbutanil, cyproconazole cyproconazole), tebuconazole, hexaconazole
  • a bactericidal compound generator name; including partial application, or
  • the amount of flonicamid treated varies depending on the conditions of the target crop, treatment method, formulation form, etc., and is generally difficult to define, but is usually 0.1 to 24,000 g / ha.
  • the treatment amount of flonicamid is usually 0.1 to 10,000 g / ha, preferably 1 to 1,000 g / ha, more preferably 10 to 500 g / ha, and further The preferred range is 25 to 500 g / ha.
  • the treatment amount of flonicamid is usually 5 to 1,000 g / ha, desirably 10 to 1,000 g / ha, and more desirably 50 to 600 g / ha.
  • the treatment amount of flonicamid is usually 0.001 to 100 g / box, preferably 0.01 to 10 g / box, and more preferably 0.1 to 5 g / box.
  • the effective concentration of flonicamid is 0.05 to 7,000 ppm, desirably 0.5 to 700 ppm, more desirably 0.5 to 350 ppm, and still more desirably 0.8 to 200 ppm.
  • a mating behavior disturbing agent for a parasitic parasitic insect of rice containing flonicamid as an active ingredient (2) The mating behavior disruptor according to (1), wherein the pest is at least one selected from the group consisting of planthoppers and leafhoppers. (3) The mating behavior disruptor according to (1), wherein the pest is a planthopper. (4) A method for controlling a copulation behavior disruptor of a rice parasitic sucking pest containing flonicamid as an active ingredient to control the pest. (5) A method for disturbing the mating behavior of a pest of rice parasitic juice pests containing flonicamid as an active ingredient by treating the agent.
  • a pest control composition comprising flonicamid and a poorly water-soluble resin.
  • a composition for controlling pests, wherein the composition according to (25) to (27) or (29) is a granule.
  • Formulation Example 1 After mixing 1 part by weight of flonicamid, 20 parts by weight of bentonite (manufactured by Toyoshun Kogyo Co., Ltd.) and 76 parts by weight of powdered calcium carbonate (manufactured by Shimizu Kogyo Co., Ltd.), Toxanone GR-31A (polycarboxylate aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.) ) 3 parts by weight, 3 parts by weight of Sun Extract C (calcium lignin sulfonate, manufactured by Nippon Paper Chemical Co., Ltd.) and the required amount of water are kneaded, granulated by an extrusion granulator, dried and sized. A pesticide granule was obtained.
  • bentonite manufactured by Toyoshun Kogyo Co., Ltd.
  • powdered calcium carbonate manufactured by Shimizu Kogyo Co., Ltd.
  • Toxanone GR-31A polycarbox
  • Formulation Example 2 After mixing 2 parts by weight of flonicamid, 92.3 parts by weight of powdered calcium carbonate, and 3 parts by weight of polyoxyethylene styryl phenyl ether sulfate (Solpol 5096, manufactured by Toho Chemical Industry Co., Ltd.), an ethylene / acrylic acid copolymer was mixed with 27 w / w. % Aqueous emulsion (trade name: HYTEC S-3111 (manufactured by Toho Chemical Industry Co., Ltd.)), add the required amount, knead, granulate with an extruder, dry and sizing to obtain agrochemical granules It was.
  • HYTEC S-3111 manufactured by Toho Chemical Industry Co., Ltd.
  • Formulation Example 3 After mixing 2 parts by weight of flonicamid, 92.3 parts by weight of clay and 3 parts by weight of polyoxyethylene styryl phenyl ether sulfate (Solpol 5096, manufactured by Toho Chemical Industry Co., Ltd.), 27% w / w ethylene / acrylic acid copolymer is contained. Add 10 parts by weight of an aqueous emulsion (trade name: HYTEC S-3121 (manufactured by Toho Chemical Industry Co., Ltd.)), add the necessary amount, knead, granulate with an extruder, dry and sizing to obtain agrochemical granules.
  • HYTEC S-3121 manufactured by Toho Chemical Industry Co., Ltd.
  • Test Example 1 Control effect against brown planthopper by treatment with flonicamid seedling box 1.2 mg ⁇ 1.2 cm cell seedlings (3 / strain) at a ratio of 1.5 mg ai / strain, prepared according to Formulation Example 1
  • the agent was processed in a nursery box.
  • One day after the flonicamid treatment the rice was extracted from the cell together with the soil, transplanted one strain per pot, and the water depth was maintained at 3 cm.
  • Two small greenhouses were prepared, and 24 pots for flonicamid treatment and no treatment were installed in each small greenhouse. Ten , 17 and 30 days after transplanting, 100 adults of Nilaparvata lugens / greenhouse were released.
  • Test Example 2 Mating behavior disturbing action against a brown planthopper 10 seeds of rice were sown on 40 mm ⁇ 40 mm absorbent cotton to prepare a rice seedling having a height of about 5 cm. Rice seedlings were immersed in an aqueous solution containing 200 ppm of the active ingredient flonicamid, air-dried, and placed in a glass vial (inner diameter 40 mm ⁇ height 75 mm; capacity 50 ml). An adult non-mating leafhopper ( Nilaparvata lugens ) raised from the age of the old larvae was bred with drug-untreated rice seedlings. From the 6th day after emergence, the animals were bred on immersion-treated rice for 24 hours.
  • next-generation larvae was measured by comparing the number of newly born next-generation larvae in immersion-treated rice seedlings (flonicamide treated group) and drug-untreated rice seedlings (untreated group). Moreover, when one male and one female were put together, they were observed for 2 hours to confirm the presence or absence of mating behavior. In order to confirm that no next-generation larvae were generated in an unmated state, an unmated female was bred alone in an untreated group, and the number of next-generation larvae was measured (unmated group). The results are shown in Table 2.
  • Test Example 3 Mating behavior disruptive effect on a brown planthopper line that is less sensitive to neonicotinoid insecticides
  • the testimony of the planthopper of Test Example 2 is less sensitive to the common name imidacloprid, a typical neonicotinoid insecticide
  • the same test was conducted in place of the brown planthopper, and the number of next-generation larvae was measured in comparison with the flonicamid treated group and the untreated group. The results are shown in Table 3.
  • Test example 4 Disrupting effect of mating behavior on white- spotted plant
  • the white- spotted planthopper in Test example 2 was replaced with a white- spotted planthopper ( Sogatella furcifera ), and the same test was conducted. Was measured. The results are shown in Table 4.
  • Test Example 5 Mating behavior disruption effect on Japanese brown planthopper
  • the Japanese brown planthopper of Test Example 2 was replaced with Japanese brown planthopper ( Laodelphax striatella ), and the same test was carried out.
  • the number of next-generation larvae compared with the flonicamid treated group and the untreated group was measured. The results are shown in Table 5.
  • Test Example 6 Disturbance of mating behavior against brown planthopper A rice seedling was tested according to Test Example 2 except that it was treated with an aqueous solution containing the active ingredients flonicamid 50, 12.5, 3.1 and 0.8 ppm. It was. Table 6 shows the results of measuring the number of generations of next-generation larvae in comparison with the flonicamid-treated group and the non-treated group.
  • Test Example 7 Mating Action Disturbing Action on White-Spotted Plant A rice seedling was tested according to Test Example 4 except that it was treated with an aqueous solution containing the active ingredients flonicamid 50, 12.5 and 3.1 ppm. Table 7 shows the results of measuring the number of generations of next-generation larvae in comparison with the flonicamid-treated group and the untreated group.
  • Test Example 8 Mating Behavior Disturbing Action for Brown Bean Spike A test was conducted according to Test Example 5 except that rice seedlings were treated with an aqueous solution containing the active ingredients flonicamid 50, 12.5, and 3.1 ppm. Table 8 shows the results of measuring the number of generations of next-generation larvae in comparison with the flonicamid-treated group and the non-treated group.
  • Test Example 9 Mating behavior disturbing action against a brown planthopper line that is less sensitive to neonicotinoid insecticides Tested according to Test Example 3 except that rice seedlings were treated with an aqueous solution containing 0.8 ppm of the active ingredient flonicamid Went. Table 9 shows the results of measuring the number of generations of next-generation larvae in comparison with the flonicamid-treated group and the non-treated group.
  • Test Example 10 Mating behavior disturbing action against leafhopper leafhopper
  • leafhopper leafhopper Nephotettix cincticeps
  • rice seedlings were treated with flonicamid treated with an aqueous solution containing the active ingredient flonicamid 200, 50 ppm.
  • the number of next-generation larvae was measured in comparison with the ward and the untreated ward. The results are shown in Table 10.
  • Test Example 11 Control effect against brown planthopper by treatment with flonicamid nursery box A pest control composition prepared according to Formulation Example 2 in a ratio of 6, 12, 24 and 36 g ai / box in a 30 cm ⁇ 60 cm nursery box Processed. Untreated zone and dinotefuran granule (trade name: Starkle box granule, manufactured by Mitsui Chemicals Agro) Treatment zone (24 g ai / box) and imidacloprid granule (trade name: Admeier box granule, manufactured by Bayer CropScience) A treatment zone (24 g ai / box) was installed.
  • FIG. 2 shows a graph of the flonicamid-treated section as a representative example of the 24 g ai / 10a flonicamid-treated section.
  • ⁇ - ⁇ black circle
  • ⁇ - ⁇ white square mark
  • xx x mark
  • the present invention is particularly useful in the situation of controlling rice parasitic sap pests where there is a demand to suppress the increase in the number of insect pests as long as possible after the chemical treatment.
  • Test Example 12 Control effect against brown planthopper by treatment with flonicamid stalks and leaves The plant was transplanted to a field of 32 m 2 in 1 ward by a rice planting machine. 36, 43, 51, 57, and 65 days after transplantation, 500 adults of brown planthopper and 12,000 eggs were released on 100 m 2 of the field. 70 days after transplantation, flonicamid was treated with foliacamide at a heading period with a spraying amount of 150 L / 10a.
  • the present invention can be used for controlling planthoppers that are sucking pests that are regarded as major pests in the field of rice cultivation. It should be noted that the entire contents of the specification, claims, drawings and abstract of Japanese Patent Application 2010-170936 filed on July 29, 2010 are cited herein as disclosure of the specification of the present invention. Incorporated.

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  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Pest Control & Pesticides (AREA)
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Abstract

A copulation disruption agent for sap-sucking pests which are considered the principal pests in rice cultivation is disclosed. Applying flonicamid to sap-sucking pests that affect rice cultivation disrupts the copulatory behavior thereof, effecting stable, effective pest control over the long term. This is a completely unpredicted effect, distinctly different from the simple pesticidal use of flonicamid. Disclosed are: a copulation disruption agent for sap-sucking rice parasites, said agent containing flonicamid as an active ingredient; and a method, in which said copulation disruption agent is processed, for disrupting the copulatory behavior of the aforementioned pests.

Description

吸汁害虫の交尾行動かく乱剤Mating behavior disruptor for sucking pests
 本発明は、吸汁害虫の交尾行動かく乱剤に関する。 The present invention relates to a copulation disruption agent for sucking pests.
 N-シアノメチル-4-トリフルオロメチル-3-ピリジンカルボキサミド(一般名フロニカミド(flonicamid))は、特許文献1に化合物No.1として記載されている化合物である。特許文献2には、フロニカミドを含むピリジン系化合物と各種効力増強成分とを含有する有害生物防除剤組成物が記載されている。 N-cyanomethyl-4-trifluoromethyl-3-pyridinecarboxamide (generic name flonicamid) is a compound described as Patent No. 1 in Patent Document 1. Patent Document 2 describes a pesticidal composition containing a pyridine-based compound containing flonicamid and various efficacy enhancing components.
ヨーロッパ特許公報第580374号European Patent Publication No. 580374 国際公開公報 WO 2009/128409International Publication Gazette WO 2009/128409
 稲作分野において主要な害虫とされている吸汁害虫であるウンカ類は、増殖力が高く、イネに対して甚大な被害を引き起こす。特にトビイロウンカは収穫期までの間に複数世代に亘って増殖を繰り返し、イネの坪枯れを起こすことが主たる被害である。坪枯れとは、トビイロウンカの吸汁害により、イネが枯死及び/又は倒伏する被害のことである。現在、ウンカ類に対する防除剤は、ネオニコチノイド系殺虫剤が主流であるが、近年急激に、ネオニコチノイド系殺虫剤に対して感受性の低下したウンカ類が見られるようになったことから、稲作分野において、ネオニコチノイド系殺虫剤に置き換わり、新たな主流となり得る防除剤又は防除方法が希求されている。 Root beetles, which are sucking pests that are regarded as the main pests in the field of rice cultivation, have a high growth potential and cause enormous damage to rice. In particular, the brown planthopper repeatedly grows over a number of generations until the harvest season, and the main damage is caused by the dryness of rice. “Tsubo withering” refers to the damage that rice dies and / or surrenders due to the sucking damage of the brown planthopper. At present, neonicotinoid insecticides are the mainstream as a control agent for planthoppers, but recently, planthoppers with reduced susceptibility to neonicotinoid insecticides have been seen. In the field of rice cultivation, there is a demand for a control agent or control method that can replace neonicotinoid insecticides and become a new mainstream.
 トビイロウンカの生態は特徴的であり、本発明者らは、トビイロウンカを含めたウンカ類の防除において、その特徴的な生態に関連付けて研究を行った。
 トビイロウンカはベトナム以北の地域では越冬できない。例えば日本では、主に6月下旬~7月の梅雨期に海外から下層ジェット気流に乗って飛来してくる長翅型成虫が発生源となる。飛来密度は、同じく海外飛来性のセジロウンカに比べてかなり低く、飛来した時点での寄生密度では大きな問題は引き起こさない。
 しかし、飛来後、雌成虫は約4日間の産卵前期間を経てイネ葉鞘の組織内に産卵し、25℃では卵期間7~9日、幼虫期間14日を経て次世代(第1世代)成虫となる。第1世代の雌成虫は増殖率の高い短翅型となることが多い。短翅型雌はあまり移動せず、産卵数も多いため、第2世代個体群は局所的に、しかも幾何級数的に密度が高くなり、第2世代又は第3世代の発生時期に、坪枯れを引き起こす。
 また、トビイロウンカが越冬できるベトナム以南の東南アジア諸国においても、上記のような、局所的な増殖及び坪枯れによる甚大な被害が生じることは同様である。
 さらに、現状では、トビイロウンカの卵に対して有効で、且つ環境及び益虫に対する安全性を有する農薬は見出されていない。
 このようなことから、本発明者らは、トビイロウンカの被害を防ぐ方法を見出すべく、飛来成虫及び第1世代成虫に産卵させないこと、産卵させにくくすること及び卵が孵化しないようにすることなど、害虫の次世代個体数や密度を低下させることに着目した。
The ecology of the green planthopper is characteristic, and the present inventors conducted research in connection with the characteristic ecology in the control of planthoppers including the green planthopper.
Tobiro planta cannot overwinter in areas north of Vietnam. For example, in Japan, the long-winged adult worms that fly from the lower part of the jet stream from overseas during the rainy season from late June to July are the source. The flying density is considerably lower than that of the overseas flying white smelt, and the parasitic density at the time of flying does not cause a big problem.
However, after flight, adult females lay eggs in the tissue of rice leaf sheaths after a pre-laying period of about 4 days, and at 25 ° C, the next generation (first generation) adults after an egg period of 7-9 days and a larval period of 14 days. It becomes. First-generation female adults often have short wings with a high growth rate. Short-cage females do not move much and have a large number of eggs, so the second generation population is locally and geometrically dense, and witheres at the time of the second or third generation. cause.
In Southeast Asian countries in the sub-Vietnam where the brown planthopper can winter, the same damage as described above is caused by local growth and withering.
Furthermore, at present, no pesticide has been found that is effective against brown planthopper eggs and has safety to the environment and beneficial insects.
From such things, the present inventors, in order to find a method to prevent the damage of the brown planthopper, do not spawn adult adults and first generation adults, make it difficult to spawn and prevent eggs from hatching, etc. We focused on reducing the next generation population and density of pests.
 その結果、本発明者らは、各種農薬有効成分の中でもフロニカミドが前記課題を解決する、吸汁害虫の交尾行動かく乱作用を持つことを見出し、本発明を完成させた。本発明における交尾行動かく乱作用とは、メスが腹部の振動でオスを呼ぶ行動を抑制し、オスがメスを探す一連の交尾行動を抑制する作用を言う。このように交尾行動をかく乱された結果、メスの産卵数は減少し、更に、産卵された卵は未受精卵であるため孵化しない。
 即ち、本発明は、フロニカミドを吸汁害虫に作用させることにより、吸汁害虫を防除する方法、吸汁害虫の次世代個体数を低下させる方法及び吸汁害虫の交尾行動をかく乱する方法に関する。
As a result, the present inventors have found that flonicamid, among various active ingredients of agricultural chemicals, has the effect of disturbing the copulation behavior of sucking pests, which solves the above problems, and completed the present invention. The copulation behavior disturbing action in the present invention refers to an action of suppressing a series of mating actions in which a female searches for a female by suppressing the action of calling the male by vibration of the abdomen. As a result of disturbing the mating behavior in this way, the number of female laying eggs decreases, and furthermore, the eggs laid are not hatched because they are unfertilized eggs.
That is, the present invention relates to a method for controlling sucking pests by causing flonicamid to act on sucking pests, a method for reducing the next generation population of sucking pests, and a method for disturbing the mating behavior of sucking pests.
 本発明の吸汁害虫の交尾行動かく乱剤及び防除方法は、長期間に亘って安定した高い防除効果を奏することができる。
 また、本発明は、フロニカミドの単純な殺有害生物剤としての使用とは一線を画す、害虫の次世代個体数を低下させるという全く予期されなかった効果を奏するものである。例えば、育苗箱処理を行った場合、従来用いられてきた防除剤では、長期間の残効が期待できないため散布剤を複数回処理する必要があるが、本発明の方法においては、少なくとも、散布剤処理の回数を軽減することが可能である。本発明が開示する「害虫の次世代個体数を低下させる」という全く予期されなかった効果を応用し、例えば育苗箱処理に適用した場合、通常所望される十分な長期間に亘って吸汁害虫防除効果が発揮される。
The mating behavior disrupting agent and control method for sucking pests according to the present invention can exhibit a stable and high control effect over a long period of time.
In addition, the present invention is completely different from the use of flonicamid as a simple pesticide, and has an unexpected effect of reducing the next-generation population of pests. For example, when a seedling box treatment is performed, a conventionally used control agent cannot be expected to have a long-lasting residual effect, and therefore it is necessary to treat the spray agent a plurality of times. It is possible to reduce the number of times of agent treatment. Applying the completely unexpected effect of “reducing the next generation of pests” disclosed by the present invention, for example, when applied to a seedling box treatment, it is usually desired to control sucking pests over a sufficiently long period of time. The effect is demonstrated.
フロニカミド粒剤の育苗箱処理によるトビイロウンカ成虫放飼試験を行った際の次世代個体数抑制効果の結果を示すグラフである。It is a graph which shows the result of the next generation population suppression effect at the time of conducting the adult flying planthopper release test by the seedling box processing of flonicamid granule. フロニカミド育苗箱処理用粒剤の育苗箱処理によるトビイロウンカ成虫放飼試験を行った際の次世代個体数抑制効果の結果を示すグラフである。It is a graph which shows the result of the next generation population suppression effect at the time of conducting the adult planthopper release test by the seedling box process of the granule for flonicamid seedling box process.
 本発明における農薬有効成分はフロニカミドである。フロニカミド(flonicamid)は一般名であり、その化学名はN-シアノメチル-4-トリフルオロメチル-3-ピリジンカルボキサミドである。フロニカミドは塩を形成する場合がある。 The active ingredient for agricultural chemicals in the present invention is flonicamid. Flonicamid is a common name and its chemical name is N-cyanomethyl-4-trifluoromethyl-3-pyridinecarboxamide. Flonicamid may form a salt.
 本発明においてイネ寄生吸汁害虫は、ウンカ類、ヨコバイ類、カメムシ類等が挙げられる。
 ウンカ類はトビイロウンカ、セジロウンカ、ヒメトビウンカ等が挙げられ、ヨコバイ類はツマグロヨコバイ等が挙げられ、カメムシ類はアカスジカスミカメ、アカヒゲホソミドリカスミカメ等が挙げられる。
 本発明において前記吸汁害虫は、好ましくはウンカ類及びヨコバイ類が挙げられる。より好ましくはウンカ類が挙げられる。
 更に好ましくはトビイロウンカが挙げられる。
 本発明の防除対象である前記吸汁害虫には、ネオニコチノイド系殺虫剤に感受性が低下した吸汁害虫が挙げられる。
In the present invention, examples of the rice parasitic sucking insects include planthoppers, leafhoppers, and stink bugs.
The planthoppers include brown planthoppers, white-spotted planthoppers, and leafhoppers. The leafhoppers include leafhopper leafhoppers and the like, and the stink bugs include akazikakasomika and akahigehosomidorikamikameka.
In the present invention, the soup pests preferably include planthoppers and leafhoppers. More preferably, a planthopper is mentioned.
More preferred is a brown planthopper.
Examples of the sucking pests to be controlled according to the present invention include sucking pests having reduced sensitivity to neonicotinoid insecticides.
 本発明において、フロニカミドと、ノニオン系界面活性剤、アニオン系界面活性剤、カチオン系界面活性剤、両性界面活性剤、動植物油、鉱物油、水溶性高分子、樹脂及びワックスから成る群から選択された少なくとも1種の効力増強成分を併用することができる。 In the present invention, flonicamid is selected from the group consisting of nonionic surfactants, anionic surfactants, cationic surfactants, amphoteric surfactants, animal and vegetable oils, mineral oils, water-soluble polymers, resins and waxes. In addition, at least one efficacy enhancing component can be used in combination.
 本発明においてフロニカミドは、従来の農薬製剤の場合と同様に、各種補助剤と配合し、乳剤、粉剤、水和剤、液剤、粒剤、懸濁製剤等の種々の形態に製剤することができる。ここにいう補助剤としては、担体、懸濁剤、増粘剤、安定剤、分散剤、湿潤剤、浸透剤、凍結防止剤、消泡剤等が挙げられ、必要により適宜添加すればよい。担体としては、固体担体と液体担体に分けられ、固体担体としては、澱粉、砂糖、セルロース粉、シクロデキストリン、活性炭、大豆粉、小麦粉、もみがら粉、木粉、魚粉、粉乳等の動植物性粉末;タルク、カオリン、ベントナイト、有機ベントナイト、炭酸カルシウム、硫酸カルシウム、重炭酸ナトリウム、ゼオライト、ケイソウ土、ホワイトカーボン、クレー、アルミナ、シリカ、硫黄粉末、消石灰等の鉱物性粉末等が挙げられ、液体担体としては、水;エチルアルコール、エチレングリコール等のアルコール類;アセトン、メチルエチルケトン、メチルイソブチルケトン、イソホロン等のケトン類;ジオキサン、テトラヒドロフラン等のエーテル類;ケロシン、灯油、流動パラフィン等の脂肪族炭化水素類;トルエン、キシレン、トリメチルベンゼン、テトラメチルベンゼン、シクロヘキサン、ソルベントナフサ等の芳香族炭化水素類;クロロホルム、クロロベンゼン等のハロゲン化炭化水素類;N,N-ジメチルホルムアミド等の酸アミド類;酢酸エチルエステル、脂肪酸のグリセリンエステル等のエステル類;アセトニトリル等のニトリル類;ジメチルスルホキシド等の含硫化合物類或いはN-メチル-2-ピロリドン等が挙げられる。分散剤としてはポリカルボン酸またはその塩、リグニンスルホン酸またはその塩等が挙げられる。前記効力増強成分を用いる場合は、フロニカミドと、前記効力増強成分を一緒に混合・製剤しても良いし、或いは別々に製剤してそれらを混合しても良い。これら製剤品の実際の使用に際しては、そのまま使用するか、又は水等の希釈剤で所定濃度に希釈して使用することができる。 In the present invention, flonicamid can be formulated in various forms such as emulsions, powders, wettable powders, liquids, granules, suspensions and the like by blending with various adjuvants as in the case of conventional agricultural chemical preparations. . Examples of the auxiliary agent include a carrier, a suspending agent, a thickening agent, a stabilizer, a dispersing agent, a wetting agent, a penetrating agent, an antifreezing agent, an antifoaming agent, and the like. Carriers are divided into solid carriers and liquid carriers, and solid carriers include starch, sugar, cellulose powder, cyclodextrin, activated carbon, soybean powder, wheat flour, rice bran powder, wood powder, fish powder, milk powder, and other animal and vegetable powders. Talc, kaolin, bentonite, organic bentonite, calcium carbonate, calcium sulfate, sodium bicarbonate, zeolite, diatomaceous earth, white carbon, clay, alumina, silica, sulfur powder, mineral powder such as slaked lime, etc., liquid carrier As: water; alcohols such as ethyl alcohol and ethylene glycol; ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, and isophorone; ethers such as dioxane and tetrahydrofuran; and aliphatic hydrocarbons such as kerosene, kerosene, and liquid paraffin Toluene, xylene, tri Aromatic hydrocarbons such as tilbenzene, tetramethylbenzene, cyclohexane and solvent naphtha; Halogenated hydrocarbons such as chloroform and chlorobenzene; Acid amides such as N, N-dimethylformamide; Acetic acid ethyl ester, fatty acid glycerin ester, etc. And nitriles such as acetonitrile; sulfur-containing compounds such as dimethyl sulfoxide; N-methyl-2-pyrrolidone and the like. Examples of the dispersant include polycarboxylic acid or a salt thereof, lignin sulfonic acid or a salt thereof, and the like. When using the efficacy enhancing component, flonicamid and the efficacy enhancing component may be mixed and formulated together, or separately formulated and mixed. In actual use of these preparations, they can be used as they are or after diluting to a predetermined concentration with a diluent such as water.
 本発明においてフロニカミドは、育苗箱に処理したり、水田に処理したりすることができる。本発明の方法では、吸汁害虫に吸汁させることにより特に大きな顕著な効果を奏することから、育苗箱処理が望ましい。水溶解度の高い農薬有効成分であるフロニカミドは、育苗箱処理によりイネの根部からの薬剤吸い上げ作用により、効率的に植物体内に取り込ませることができるからである。 In the present invention, flonicamid can be treated in a nursery box or treated in a paddy field. In the method of the present invention, a seedling box treatment is desirable because a particularly significant effect can be achieved by sucking the soup pest. This is because flonicamid which is an active ingredient of agricultural chemicals having high water solubility can be efficiently taken into the plant body by the action of sucking up the drug from the root of rice by the seedling box treatment.
 本発明においては、前記したようにフロニカミドを各種の形態に製剤することができるが、育苗箱処理が望ましいとの観点から、中でも育苗箱処理用の粒剤とすることが望ましい。
 本発明の効果を発揮させるために適した育苗箱処理用の粒剤としては、フロニカミドと難水溶性樹脂を含有する組成物で、製剤中でフロニカミドと難水溶性樹脂がマトリックス、即ちフロニカミドが難水溶性樹脂に取り込まれた組成物を形成していることを特徴とする組成物が挙げられ、以下に詳述する。
In the present invention, flonicamid can be formulated into various forms as described above, but from the viewpoint that the seedling box treatment is desirable, it is desirable to use a granule for the seedling box treatment.
As a granule for treatment of a seedling box suitable for exerting the effects of the present invention, a composition containing flonicamid and a poorly water-soluble resin is used. In the preparation, flonicamid and the poorly water-soluble resin are difficult to form a matrix, that is, flonicamid is difficult. The composition characterized by forming the composition taken in by water-soluble resin is mentioned, It mentions in full detail below.
 本発明に用いる有効成分フロニカミドは、水溶解度が非常に高い化合物(20℃における水溶解度:5200mg/L)であることが知られている。育苗箱処理用の薬剤は、長期に薬効を持続させる必要があるため、農薬有効成分の溶出を制御することが求められる一方で、フロニカミドのような水溶解度の極めて高い化合物を本使用態様に適用させることは困難とされてきた。前記組成物は、前記フロニカミドの水溶解度に起因する問題を解消する上で有効な一態様である。配合量については0.1~30重量%、好ましくは0.5~25重量%である。
 本発明で使用するフロニカミドの平均粒子径は、1~500μm、望ましくは1~100μm、更に望ましくは5~50μmである。
 本発明で使用することのできる難水溶性樹脂としては、エチレン・酢酸ビニル共重合体、エチレン・アクリル酸共重合体、エチレン・ベオバ共重合体、スチレン・アクリル酸共重合体、アクリル酸エステル、アクリル・シリコン共重合体、酸化ポリエチレン、ウレタン樹脂、石油樹脂などを挙げることができる。難水溶性樹脂はエマルションとして使用することが望ましく、特に、エチレン・アクリル酸共重合体エマルションが望ましい。エチレン・アクリル酸共重合体エマルションとしては、例えば、HYTEC S-3111、HYTEC S-3121、HYTEC S-3127(東邦化学工業社製)などが挙げられる。これらの樹脂エマルションは単独で使用されるのみならず混合して使用することもできる。配合量については固形分で0.1~30重量%、好ましくは1~15重量%である。
 本発明に使用する担体としては、特に限定されないが、例えば、クレー、ベントナイト、タルク、炭酸カルシウム、ジークライト、セリサイト、酸性白土、珪藻土、ゼオライト、パーライト、アタパルジャイトなどの担体を使用することができる。配合量については、特に制限されないが、40~99.8重量%、好ましくは60~98.5重量%の範囲内である。
 前記組成物は、難水溶性樹脂を使用するため水とのなじみが悪く、本田移植後に薬剤が浮遊することがあるため、湿潤剤を添加することが望ましい。湿潤剤としては、ジオクチルスルホコハク酸ナトリウム、アルキルベンゼンスルホン酸ナトリウム、高級アルコール硫酸エステル、アルキルナフタレンスルホン酸ナトリウム、ポリオキシエチレンフェニルエーテルサルフェート、ポリオキシエチレンスチリルフェニルエーテルサルフェート、ポリオキシエチレンアルキルエーテルなどが挙げられ、望ましくは、ポリオキシエチレンスチリルフェニルエーテルサルフェートが挙げられる。これらの湿潤剤は単独で使用されるのみならず混合して使用することもできる。湿潤剤を使用する場合、配合量については特に制限されないが、0.01~10重量%、好ましくは0.1~5重量%である。
 前記組成物は、農薬の製造において通常用いられる造粒法、例えば、押し出し造粒法、転動造粒法、転動流動造粒法、流動層造粒法、圧縮造粒法、攪拌混合造粒法、被覆造粒法、打錠法などにより調製することができる。
 例えば、フロニカミド、湿潤剤及び担体を均一に混合した後、難水溶性樹脂エマルションを加えてニーダーなどで混練し、ドームグランなど押出し造粒機により造粒し、乾燥、整粒することにより前記組成物を得ることができる。
 また、前記組成物は、所望により溶出速度を更に制御するため、パラフィン等の溶出制御剤を添加することができる。
 前記組成物には、以上述べた成分以外に、任意成分として、例えば、本発明の農薬製剤中で農薬活性成分を安定に保つ目的および/または造粒する際の造粒性などを向上させる目的で、必要に応じて、界面活性剤、補助剤などを含有せしめることができる。
The active ingredient flonicamid used in the present invention is known to be a compound having a very high water solubility (water solubility at 20 ° C .: 5200 mg / L). Since chemicals for nursery box treatment need to maintain their efficacy over a long period of time, it is required to control the elution of active ingredients of agricultural chemicals, while a compound with extremely high water solubility such as flonicamid is applied to this usage mode. It has been difficult to do. The composition is an effective embodiment for solving the problems caused by the aqueous solubility of flonicamid. The blending amount is 0.1 to 30% by weight, preferably 0.5 to 25% by weight.
The average particle size of flonicamid used in the present invention is 1 to 500 μm, preferably 1 to 100 μm, and more preferably 5 to 50 μm.
As the poorly water-soluble resin that can be used in the present invention, ethylene / vinyl acetate copolymer, ethylene / acrylic acid copolymer, ethylene / veova copolymer, styrene / acrylic acid copolymer, acrylic ester, Acrylic / silicone copolymer, polyethylene oxide, urethane resin, petroleum resin and the like can be mentioned. The poorly water-soluble resin is desirably used as an emulsion, and in particular, an ethylene / acrylic acid copolymer emulsion is desirable. Examples of the ethylene / acrylic acid copolymer emulsion include HYTEC S-3111, HYTEC S-3121, and HYTEC S-3127 (manufactured by Toho Chemical Industry Co., Ltd.). These resin emulsions can be used alone or in combination. The blending amount is 0.1 to 30% by weight, preferably 1 to 15% by weight in terms of solid content.
The carrier used in the present invention is not particularly limited, and for example, a carrier such as clay, bentonite, talc, calcium carbonate, gericite, sericite, acid clay, diatomaceous earth, zeolite, perlite, attapulgite and the like can be used. . The blending amount is not particularly limited, but is in the range of 40 to 99.8% by weight, preferably 60 to 98.5% by weight.
Since the composition uses a poorly water-soluble resin, it does not fit well with water, and the drug may float after transplantation into Honda. Therefore, it is desirable to add a wetting agent. Examples of the wetting agent include sodium dioctyl sulfosuccinate, sodium alkylbenzene sulfonate, higher alcohol sulfate ester, sodium alkyl naphthalene sulfonate, polyoxyethylene phenyl ether sulfate, polyoxyethylene styryl phenyl ether sulfate, polyoxyethylene alkyl ether, and the like. Desirably, polyoxyethylene styryl phenyl ether sulfate is used. These wetting agents can be used alone or in combination. When a wetting agent is used, the blending amount is not particularly limited, but is 0.01 to 10% by weight, preferably 0.1 to 5% by weight.
The composition is a granulation method usually used in the production of agricultural chemicals, for example, extrusion granulation method, tumbling granulation method, tumbling fluidized granulation method, fluidized bed granulation method, compression granulation method, stirring and granulation method. It can be prepared by a granulation method, a coating granulation method, a tableting method or the like.
For example, after uniformly mixing flonicamid, a wetting agent and a carrier, adding a slightly water-soluble resin emulsion, kneading with a kneader, etc., granulating with an extrusion granulator such as Dome Gran, drying, and sizing You can get things.
In addition, an elution control agent such as paraffin can be added to the composition to further control the elution rate as desired.
In the composition, in addition to the components described above, as an optional component, for example, the purpose of stably maintaining the pesticidal active ingredient in the pesticidal formulation of the present invention and / or the purpose of improving the granulation property when granulating Thus, a surfactant, an auxiliary agent and the like can be contained as necessary.
 本発明においては、必要に応じてフロニカミド以外の農薬成分、例えば、殺菌剤、殺虫剤、殺ダニ剤、殺線虫剤、抗ウイルス剤、誘引剤、除草剤、植物成長調整剤などと、混用、併用することができ、この場合には一層優れた効果を示すこともある。例えば、適用範囲、薬剤処理の時期、防除活性等を好ましい方向へ改良することが可能である。尚、フロニカミドと他の農薬の有効成分化合物は各々別々に製剤したものを散布時に混合して使用しても、両者を一緒に製剤して使用してもよい。例えば、前記組成物を調製する場合、フロニカミドとそれ以外の農薬成分とも一緒に製剤できる。本発明には、このように有効成分を混合して施用する場合も含まれる。 In the present invention, if necessary, agrochemical components other than flonicamid, such as fungicides, insecticides, acaricides, nematicides, antiviral agents, attractants, herbicides, plant growth regulators, etc. Can be used in combination, and in this case, a more excellent effect may be exhibited. For example, it is possible to improve the application range, the timing of chemical treatment, the control activity, and the like in a preferable direction. Flonicamid and the other active ingredient compounds of other agricultural chemicals may be prepared separately and mixed at the time of spraying, or both may be used together. For example, when preparing the composition, it can be formulated together with flonicamid and other agrochemical ingredients. The present invention includes a case where the active ingredients are mixed and applied in this way.
 上記他の農薬中の、殺虫剤、殺ダニ剤、殺線虫剤或いは殺土壌害虫剤の有効成分化合物、すなわち殺虫性化合物(一般名;一部申請中を含む、又は試験コード)としては、例えばプロフェノホス(profenofos)、ジクロルボス(dichlorvos)、フェナミホス(fenamiphos)、フェニトロチオン(fenitrothion)、EPN、ダイアジノン(diazinon)、クロルピリホス(chlorpyrifos)、クロルピリホスメチル(chlorpyrifos‐methyl)、アセフェート(acephate)、プロチオホス(prothiofos)、ホスチアゼート(fosthiazate)、カズサホス(cadusafos)、ジスルホトン(dislufoton)、イソキサチオン(isoxathion)、イソフェンホス(isofenphos)、エチオン(ethion)、エトリムホス(etrimfos)、キナルホス(quinalphos)、ジメチルビンホス(dimethylvinphos)、ジメトエート(dimethoate)、スルプロホス(sulprofos)、チオメトン(thiometon)、バミドチオン(vamidothion)、ピラクロホス(pyraclofos)、ピリダフェンチオン(pyridaphenthion)、ピリミホスメチル(pirimiphos-methyl)、プロパホス(propaphos)、ホサロン(phosalone)、ホルモチオン(formothion)、マラチオン(malathion)、テトラクロルビンホス(tetrachlovinphos)、クロルフェンビンホス(chlorfenvinphos)、シアノホス(cyanophos)、トリクロルホン(trichlorfon)、メチダチオン(methidathion)、フェントエート(phenthoate)、ESP、アジンホスメチル(azinphos-methyl)、フェンチオン(fenthion)、ヘプテノホス(heptenophos)、メトキシクロル(methoxychlor)、パラチオン(paration)、ホスホカルブ(phosphocarb)、デメトン-S-メチル(demeton-S-methyl)、モノクロトホス(monocrotophos)、メタミドホス(methamidophos)、イミシアホス(imicyafos)、パラチオン-メチル(parathion-methyl)、テルブホス(terbufos)、ホスファミドン(phospamidon)、ホスメット(phosmet)、ホレート(phorate)、ホキシム(phoxim)、トリアゾホス(triazophos)のような有機リン酸エステル系化合物;
 カルバリル(carbaryl)、プロポキスル(propoxur)、アルジカルブ(aldicarb)、カルボフラン(carbofuran)、チオジカルブ(thiodicarb)、メソミル(methomyl)、オキサミル(oxamyl)、エチオフェンカルブ(ethiofencarb)、ピリミカルブ(pirimicarb)、フェノブカルブ(fenobucarb)、カルボスルファン(carbosulfan)、ベンフラカルブ(benfuracarb)、ベンダイオカルブ(bendiocarb)、フラチオカルブ(furathiocab)、イソプロカルブ(isoprocarb)、メトルカルブ(metolcarb)、キシリルカルブ(xylylcarb)、XMC、フェノチオカルブ(fenothiocarb)のようなカーバメート系化合物;
 カルタップ(cartap)、チオシクラム(thiocyclam)、ベンスルタップ(bensultap)、チオスルタップナトリウム(thiosultap-sodium)、モノスルタップ(monosultap)、ビスルタップ(bisultap)、シュウ酸水素チオシクラム(thiocyclam hydrogen oxalate)のようなネライストキシン誘導体;
 ジコホル(dicofol)、テトラジホン(tetradifon)、エンドスルファン(endosulfan)、ジエノクロル(dienochlor)、ディルドリン(dieldrin)のような有機塩素系化合物;
 酸化フェンブタスズ(fenbutatin oxide)、シヘキサチン(cyhexatin)のような有機金属系化合物;
 フェンバレレート(fenvalerate)、ペルメトリン(permethrin)、シペルメトリン(cypermethrin)、デルタメトリン(deltamethrin)、シハロトリン(cyhalothrin)、テフルトリン(tefluthrin)、エトフェンプロックス(ethofenprox)、フルフェンプロックス(flufenprox)、シフルトリン(cyfluthrin)、フェンプロパトリン(fenpropathrin)、フルシトリネート(flucythrinate)、フルバリネート(fluvalinate)、シクロプロトリン(cycloprothrin)、ラムダシハロトリン(lambda-cyhalothrin)、ピレスリン(pyrethrins)、エスフェンバレレート(esfenvalerate)、テトラメスリン(tetramethrin)、レスメスリン(resmethrin)、プロトリフェンブト(protrifenbute)、ビフェントリン(bifenthrin)、ゼータシペルメトリン(zeta-cypermethrin)、アクリナトリン(acrinathrin)、アルファシペルメトリン(alpha-cypermethrin)、アレスリン(allethrin)、ガンマシハロトリン(gamma-cyhalothrin)、シータシペルメトリン(theta-cypermethrin)、タウフルバリネート(tau-fluvalinate)、トラロメスリン(tralomethrin)、プロフルスリン(profluthrin)、ベータシペルメトリン(beta-cypermethrin)、ベータシフルトリン(beta-cyfluthrin)、メトフルトリン(metofluthrin)、フェノトリン(phenothrin)、フルメトリン(flumethrin)、デカメトリン(decamethrin)のようなピレスロイド系化合物;
 ジフルベンズロン(diflubenzuron)、クロルフルアズロン(chlorfluazuron)、テフルベンズロン(teflubenzuron)、フルフェノクスロン(flufenoxuron)、トリフルムロン(triflumuron)、ヘキサフルムロン(hexaflumuron)、ルフェヌロン(lufenuron)、ノバルロン(novaluron)、ノビフルムロン(noviflumuron)、ビストリフルロン(bistrifluron)、フルアズロン(fluazuron)のようなベンゾイルウレア系化合物;
 メトプレン(methoprene)、ピリプロキシフェン(pyriproxyfen)、フェノキシカルブ(fenoxycarb)、ジオフェノラン(diofenolan)のような幼若ホルモン様化合物;
 ピリダベン(pyridaben)のようなピリダジノン系化合物;
 フェンピロキシメート(fenpyroximate)、フィプロニル(fipronil)、テブフェンピラド(tebufenpyrad)、エチプロール(ethiprole)、トルフェンピラド(tolfenpyrad)、アセトプロール(acetoprole)、ピラフルプロール(pyrafluprole)、ピリプロール(pyriprole)のようなピラゾール系化合物;
 イミダクロプリド(imidacloprid)、ニテンピラム(nitenpyram)、アセタミプリド(acetamiprid)、チアクロプリド(thiacloprid)、チアメトキサム(thiamethoxam)、クロチアニジン(clothianidin)、ニジノテフラン(nidinotefuran)、ジノテフラン(dinotefuran)、ニチアジン(nithiazine)等のネオニコチノイド;
 テブフェノジド(tebufenozide)、メトキシフェノジド(methoxyfenozide)、クロマフェノジド(chromafenozide)、ハロフェノジド(halofenozide)等のヒドラジン系化合物;
 スピロディクロフェン(spirodiclofen)等のようなテトロニック酸系化合物;
 フルアクリピリム(fluacrypyrin)等のようなストロビルリン系化合物;
 フルフェネリム(flufenerim)等のようなピリジナミン系化合物;
 ジニトロ系化合物、有機硫黄化合物、尿素系化合物、トリアジン系化合物、ヒドラゾン系化合物、また、その他の化合物として、ブプロフェジン(buprofezin)、ヘキシチアゾクス(hexythiazox)、アミトラズ(amitraz)、クロルジメホルム(chlordimeform)、シラフルオフェン(silafluofen)、トリアザメイト(triazamate)、ピメトロジン(pymetrozine)、ピリミジフェン(pyrimidifen)、クロルフェナピル(chlorfenapyr)、インドキサカルブ(indoxacarb)、アセキノシル(acequinocyl)、エトキサゾール(etoxazole)、シロマジン(cyromazine)、1,3-ジクロロプロペン(1,3-dichloropropene)、ジアフェンチウロン(diafenthiuron)、ベンクロチアズ(benclothiaz)、ビフェナゼート(bifenazate)、スピロメシフェン(spiromesifen)、スピロテトラマット(spirotetramat)、プロパルギット(propargite)、クロフェンテジン(clofentezine)、メタフルミゾン(metaflumizone)、3-ブロモ-N-(2-ブロモ-4-クロロ-6-(1-シクロプロピルエチルカルバモイル)フェニル)-1-(3-クロロピリジン-2-イル)-1H-ピラゾール-5-カルボキサミド、3-ブロモ-N-(4-クロロ-2-(1-シクロプロピルエチルカルバモイル)-6-メチルフェニル)-1-(3-クロロピリジン-2-イル)-1H-ピラゾール-5-カルボキサミド、3-ブロモ-N-(2-ブロモ-4-クロロ-6-(シクロプロピルメチルカルバモイル)フェニル)-1-(3-クロロピリジン-2-イル)-1H-ピラゾール-5-カルボキサミド、フルベンジアミド(flubendiamide)、シフルメトフェン(cyflumetofen)、クロラントラニリプロール(chlorantraniliprole)、シアントラニリプロール(Cyantraniliprole)、シエノピラフェン(cyenopyrafen)、ピリフルキナゾン(pyrifluquinazone)、フェナザキン(fenazaquin)、アミドフルメット(amidoflumet)、クロロベンゾエート(chlorobenzoate)、スルフルアミド(sulfluramid)、ヒドラメチルノン(hydramethylnon)、メタアルデヒド(metaldehyde)、HGW-86、AKD‐1022、リアノジン(ryanodine)、ピリダリル(pyridalyl)、ベルブチン(verbutin)、チアゾリルシナノニトリル(thiazolylcinnanonitrile)のような化合物;等が挙げられる。更に、Bacillus thuringienses aizawai、Bacillus thuringienses kurstaki、Bacillus thuringienses israelensis、Bacillus thuringienses japonensis、Bacillus thuringienses tenebrionis、Bacillus thuringiensesが生成する結晶タンパク毒素、昆虫病原ウイルス剤、昆虫病原糸状菌剤、線虫病原糸状菌剤等のような微生物農薬、アベルメクチン(avermectin)、エマメクチンベンゾエート(emamectin Benzoate)、ミルベメクチン(milbemectin)、ミルベマイシン(milbemycin)、スピノサッド(spinosad)、イベルメクチン(ivermectin)、レピメクチン(lepimectin)、DE-175、アバメクチン(abamectin)、エマメクチン(emamectin)、スピネトラム(spinetoram)のような抗生物質及び半合成抗生物質;アザディラクチン(azadirachtin)、ロテノン(rotenone)のような天然物;ディート(deet)のような忌避剤;等と、混用、併用することもできる。
In the above-mentioned other agricultural chemicals, as an active ingredient compound of an insecticide, acaricide, nematicide or soil insecticide, that is, an insecticidal compound (generic name; including some pending applications or test codes), For example, profenofos, dichlorvos, fenamiphos, fenitrothion, EPN, diazinon, chlorpyrifos, chlorpyrifos-methyl, acephatethio, prothiophos , Fosthiazate, cadusafos, dislufoton, isoxathion, isofenphos, ethion, etrimfos, quinalphos, dimethylvinphos, dimethoate (dimethoate) dimethoate), sulprofos, Thiometon, bamidothion, pyraclofos, pyridaphenthion, pirimiphos-methyl, propaphos, phosalone, formothion, malathion, tetrachlorbin Phosphine (tetrachlovinphos), chlorfenvinphos, cyanophos, trichlorfon, methidathion, phenthoate, ESP, adinphos-methyl, fenthion, heptenophos ), Methoxychlor, parathion, phosphocarb, demeton-S-methyl, monocrotophos, methamidophos, imicyafos, parathion-methyl ( parathion-methyl), terb Scan (terbufos), phosphamidon (phospamidon), phosmet (phosmet), phorate (phorate), phoxim (phoxim), organic phosphoric acid ester compounds such as triazophos (triazophos);
Carbaryl, propoxur, aldicarb, carbofuran, thiodicarb, methomyl, oxamyl, ethiofencarb, pirimicarb, fenobucarb, fenobucarb Carbamates such as carbosulfan, benfuracarb, bendiocarb, furathiocab, isoprocarb, metolcarb, xylylcarb, XMC, fenothiocarb Compound;
Nereistoxins such as cartap, thiocyclam, bensultap, sodium thiosultap-sodium, monosultap, bisultap, thiocyclam hydrogen oxalate Derivatives;
Organochlorine compounds such as dicophor, tetradifon, endosulfan, dienochlor, dieldrin;
Organometallic compounds such as fenbutatin oxide and cyhexatin;
Fenvalerate, permethrin, cypermethrin, deltamethrin, cyhalothrin, tefluthrin, etofenprox, flufenprox, cyfluthrin , Fenpropathrin, flucytrinate, fluvalinate, cycloprothrin, lambda-cyhalothrin, pyrethrin, esfenvalerate, Tetramethrin, resmethrin, protrifenbute, bifenthrin, zeta-cypermethrin, acrinathrin, alpha-cypermeline (alpha-cyperme) thrin), allethrin, gamma-cyhalothrin, theta-cypermethrin, tau-fluvalinate, tralomethrin, profluthrin, beta-cypermethrin ( Pyrethroid compounds such as beta-cypermethrin, beta-cyfluthrin, mettofluthrin, phenothrin, flumethrin, decamethrin;
Diflubenzuron, chlorfluazuron, teflubenzuron, flufenoxuron, triflumuron, hexaflumuron, lufenuron, novaluron, novaluron, ), Bistrifluron, benzoylurea compounds such as fluazuron;
Juvenile hormone-like compounds such as metoprene, pyriproxyfen, fenoxycarb, diofenolan;
Pyridazinone compounds such as pyridaben;
Pyrazole compounds such as fenpyroximate, fipronil, tebufenpyrad, ethiprole, tolfenpyrad, acetoprole, pyrafluprole, pyriprole;
Imidacloprid, nitenpyram, acetamiprid, thiacloprid, thiamethoxam, clothianidin, nidinotefuran, dinotefurannit, dinotefuranoid, dinotefurannit ;
Hydrazine compounds such as tebufenozide, methoxyfenozide, chromafenozide, halofenozide;
Tetronic acid compounds such as spirodiclofen;
Strobilurin compounds such as fluacrypyrin;
Pyridinamine compounds such as flufenerim;
Dinitro compounds, organic sulfur compounds, urea compounds, triazine compounds, hydrazone compounds, and other compounds include buprofezin, hexythiazox, amitraz, chlordimeform, silafluofen ), Triazamate, pymetrozine, pyrimidifen, chlorfenapyr, indoxacarb, acequinocyl, etoxazole, cyromazine, 1,3-dichloropropene (1,3-dichloropropene), diafenthiuron, benclothiaz, bifenazate, spiromesifen, spirotetramat, propal Propargite, clofentezine, metaflumizone, 3-bromo-N- (2-bromo-4-chloro-6- (1-cyclopropylethylcarbamoyl) phenyl) -1- (3 -Chloropyridin-2-yl) -1H-pyrazole-5-carboxamide, 3-bromo-N- (4-chloro-2- (1-cyclopropylethylcarbamoyl) -6-methylphenyl) -1- (3- Chloropyridin-2-yl) -1H-pyrazole-5-carboxamide, 3-bromo-N- (2-bromo-4-chloro-6- (cyclopropylmethylcarbamoyl) phenyl) -1- (3-chloropyridine- 2-yl) -1H-pyrazole-5-carboxamide, flubendiamide, cyflumetofen, chlorant Chlorantraniliprole, cyantraniliprole, cyenopyrafen, pyrifluquinazone, fenazaquin, amidoflumet, chlorobenzoate, sulforamid, sulfluramid ), Metaldehyde, HGW-86, AKD-1022, ryanodine, pyridalyl, verbutin, thiazolylcinnanonitrile, and the like. Furthermore, Bacillus thuringienses aizawai, Bacillus thuringienses kurstaki, Bacillus thuringienses israelensis, Bacillus thuringienses japonensis, Bacillus thuringienses tenebrionis, crystalline protein toxins produced by Bacillus thuringienses, entomopathogenic fungi, nematopathogenic fungi, etc. Microbial pesticides such as avermectin, emamectin benzoate, milbemectin, milbemycin, spinosad, ivermectin, lepimectin, DE-175, abamectin ), Antibiotics such as emamectin, spinetoram and semi-synthetic antibiotics; natural products such as azadirachtin and rotenone; repellents such as deet; etc. And mixed use It is also possible to.
 上記他の農薬中の、殺菌剤の有効成分化合物、すなわち殺菌性化合物(一般名;一部申請中を含む、又は日本植物防疫協会試験コード)としては、例えば、メパニピリム(mepanipyrim)、ピリメサニル(pyrimethanil)、シプロジニル(cyprodinil)、フェリムゾン(ferimzone)のようなアニリノピリミジン系化合物;
 5-クロロ-7-(4-メチルピペリジン-1-イル)-6-(2,4,6-トリフルオロフェニル)[1,2,4]トリアゾロ[1,5-a]ピリミジンのようなトリアゾロピリミジン系化合物;
 フルアジナム(fluazinam)のようなピリジナミン系化合物;
 トリアジメホン(triadimefon)、ビテルタノール(bitertanol)、トリフルミゾール(triflumizole)、エタコナゾール(etaconazole)、プロピコナゾール(propiconazole)、ペンコナゾール(penconazole)、フルシラゾール(flusilazole)、マイクロブタニル(myclobutanil)、シプロコナゾール(cyproconazole)、テブコナゾール(tebuconazole)、ヘキサコナゾール(hexaconazole)、ファーコナゾールシス(furconazole‐cis)、プロクロラズ(prochloraz)、メトコナゾール(metconazole)、エポキシコナゾール(epoxiconazole)、テトラコナゾール(tetraconazole)、オキスポコナゾールフマル酸塩(oxpoconazole fumarate)、シプコナゾール(sipconazole)、プロチオコナゾール(prothioconazole)、トリアジメノール(triadimenol)、フルトリアホール(flutriafol)、ジフェノコナゾール(difenoconazole)、フルキンコナゾール(fluquinconazole)、フェンブコナゾール(fenbuconazole)、ブロムコナゾール(bromuconazole)、ジニコナゾール(diniconazole)、トリシクラゾール(tricyclazole)、プロベナゾール(probenazole)、シメコナゾール(simeconazole)、ペフラゾエート(pefurazoate)、イプコナゾール(ipconazole)、イミベンコナゾール(imibenconazole)のようなアゾール系化合物;
 キノメチオネート(quinomethionate)のようなキノキサリン系化合物;
 マンネブ(maneb)、ジネブ(zineb)、マンゼブ(mancozeb)、ポリカーバメート(polycarbamate)、メチラム(metiram)、プロピネブ(propineb)、チラム(thiram)のようなジチオカーバメート系化合物;
 フサライド(fthalide)、クロロタロニル(chlorothalonil)、キントゼン(quintozene)のような有機塩素系化合物;
 ベノミル(benomyl)、チオファネートメチル(thiophanate‐methyl)、カーベンダジム(carbendazim)、チアベンダゾール(thiabendazole)、フベリアゾール(fuberiazole)のようなイミダゾール系化合物;
 シモキサニル(cymoxanil)のようなシアノアセトアミド系化合物;
 メタラキシル(metalaxyl)、メタラキシル-M(metalaxyl-M)、メフェノキサム(mefenoxam)、オキサジキシル(oxadixyl)、オフレース(ofurace)、ベナラキシル(benalaxyl)、ベナラキシル-M(benalaxyl-M、別名キララキシル(kiralaxyl、chiralaxyl))、フララキシル(furalaxyl)、シプロフラム(cyprofuram)、カルボキシン(carboxin)、オキシカルボキシン(oxycarboxin)、チフルザミド(thifluzamide)、ボスカリド(boscalid)、ビキサフェン(bixafen)、イソチアニル(isotianil)、チアジニル(tiadinil)、セダキサン(sedaxane)のようなアニリド系化合物;
 ジクロフルアニド(dichlofluanid)のようなスルファミド系化合物;
 水酸化第二銅(cupric hydroxide)、有機銅(oxine copper)のような銅系化合物;
 ヒメキサゾール(hymexazol)のようなイソキサゾール系化合物;
 ホセチルアルミニウム(fosetyl‐Al)、トルクロホスメチル(tolclofos‐Methyl)、S-ベンジル O,O-ジイソプロピルホスホロチオエート、O-エチル S,S-ジフェニルホスホロジチオエート、アルミニウムエチルハイドロゲンホスホネート、エジフェンホス(edifenphos)、イプロベンホス(iprobenfos)のような有機リン系化合物;
 キャプタン(captan)、キャプタホル(captafol)、フォルペット(folpet)のようなフタルイミド系化合物;
 プロシミドン(procymidone)、イプロジオン(iprodione)、ビンクロゾリン(vinclozolin)のようなジカルボキシイミド系化合物;
 フルトラニル(flutolanil)、メプロニル(mepronil)のようなベンズアニリド系化合物;
 ペンチオピラド(penthiopyrad)、3-(ジフロロメチル)-1-メチル-N-[(1RS,4SR,9RS)-1,2,3,4-テトラヒドロ-9-イソプロピル-1,4-メタノナフタレン-5-イル]ピラゾール-4-カルボキサミドと3-(ジフロロメチル)-1-メチル-N-[(1RS,4SR,9SR)-1,2,3,4-テトラヒドロ-9-イソプロピル-1,4-メタノナフタレン-5-イル]ピラゾール-4-カルボキサミドの混合物(イソピラザム(isopyrazam))、シルチオファム(silthiopham)、フェノキサニル(fenoxanil)、フラメトピル(furametpyr)のようなアミド系化合物;
 フルオピラム(fluopyram)、ゾキサミド(zoxamide)のようなベンズアミド系化合物;
 トリホリン(triforine)のようなピペラジン系化合物;
 フロニカミド(flonicamid)、ピリフェノックス(pyrifenox)のようなピリジン系化合物;
 フェナリモル(fenarimol)のようなカルビノール系化合物;
 フェンプロピディン(fenpropidin)のようなピペリジン系化合物;
 フェンプロピモルフ(fenpropimorph)、トリデモルフ(tridemorph)のようなモルフォリン系化合物;
 フェンチンヒドロキシド(fentin hydroxide)、フェンチンアセテート(fentin acetate)のような有機スズ系化合物;
 ペンシキュロン(pencycuron)のような尿素系化合物;
 ジメトモルフ(dimethomorph)、フルモルフ(flumorph)のようなシンナミック酸系化合物;
 ジエトフェンカルブ(diethofencarb)のようなフェニルカーバメート系化合物;
 フルジオキソニル(fludioxonil)、フェンピクロニル(fenpiclonil)のようなシアノピロール系化合物;
 アゾキシストロビン(azoxystrobin)、クレソキシムメチル(kresoxim‐methyl)、メトミノストロビン(metominostrobin)、トリフロキシストロビン(trifloxystrobin)、ピコキシストロビン(picoxystrobin)、オリザストロビン(oryzastrobin)、ジモキシストロビン(dimoxystrobin)、ピラクロストロビン(pyraclostrobin)、フルオキサストロビン(fluoxastrobin)のようなストロビルリン系化合物;
 ファモキサドン(famoxadone)のようなオキサゾリジノン系化合物;
 エタボキサム(ethaboxam)のようなチアゾールカルボキサミド系化合物;
 イプロバリカルブ(iprovalicarb)、ベンチアバリカルブ-イソプロピル(benthiavalicarb-isopropyl)のようなバリンアミド系化合物;
 メチル N-(イソプロポキシカルボニル)-L-バリル-(3RS)-3-(4-クロロフェニル)-β-アラニナート(valiphenalate)のようなアシルアミノアシッド系化合物;
 フェナミドン(fenamidone)のようなイミダゾリノン系化合物;
 フェンヘキサミド(fenhexamid)のようなハイドロキシアニリド系化合物;
 フルスルファミド(flusulfamide)のようなベンゼンスルホンアミド系化合物;
 シフルフェナミド(cyflufenamid)のようなオキシムエーテル系化合物;
 アトラキノン系化合物;
 クロトン酸系化合物;
 バリダマイシン(validamycin)、カスガマイシン(kasugamycin)、ポリオキシン(polyoxins)のような抗生物質;
 イミノクタジン(iminoctadine)、ドディン(dodine)のようなグアニジン系化合物;
 6-ターシャリーブチル-8-フルオロ-2,3-ジメチルキノリン-4-イル アセテート(テブフロキン(tebufloquin))のようなキノリン系化合物;
 (Z)-2-(2-フルオロ-5-(トリフルオロメチル)フェニルチオ)-2-(3-(2-メトキシフェニル)チアゾリジン-2-イリデン)アセトニトリル(フルチアニル(flutianil))のようなチアゾリジン系化合物;
 その他の化合物として、ピリベンカルブ(pyribencarb)、イソプロチオラン(isoprothiolane)、ピロキロン(pyroquilon)、ジクロメジン(diclomezine)、キノキシフェン(quinoxyfen)、プロパモカルブ塩酸塩(propamocarb hydrochloride)クロルピクリン(chloropicrin)、ダゾメット(dazomet)、メタムナトリウム塩(metam‐sodium)、ニコビフェン(nicobifen)、メトラフェノン(metrafenone)、UBF-307、ジクロシメット(diclocymet)、プロキンアジド(proquinazid)、アミスルブロム(amisulbrom;別名アミブロドール(amibromdole))、3-(2,3,4-トリメトキシ-6-メチルベンゾイル)-5-クロロ-2-メトキシ-4-メチルピリジン、4-(2,3,4-トリメトキシ-6-メチルベンゾイル)-2,5-ジクロロ-3-トリフルオロメチルピリジン、ピリオフェノン(pyriofenone)、マンジプロパミド(mandipropamid)、フルオピコリド(fluopicolide)、カルプロパミド(carpropamid)、メプチルジノキャップ(meptyldinocap)、N-[(3', 4'-ジクロロ-1,1-ジメチル)フェナシル]-3-トリフルオロメチル-2-ピリジンカルボキサミド、N-[(3', 4'-ジクロロ-1,1-ジメチル)フェナシル]-3-メチル-2-チオフェンカルボキサミド、N-[(3', 4'-ジクロロ-1,1-ジメチル)フェナシル]-1-メチル-3-トリフルオロメチル-4-ピラゾールカルボキサミド、N-[[2'-メチル-4'-(2-プロピルオキシ)-1,1-ジメチル]フェナシル]-3-トリフルオロメチル-2-ピリジンカルボキサミド、N-[[2'-メチル-4'-(2-プロピルオキシ)-1,1-ジメチル]フェナシル]-3-メチル-2-チオフェンカルボキサミド、N-[[2'-メチル-4'-(2-プロピルオキシ)-1,1-ジメチル]フェナシル]-1-メチル-3-トリフルオロメチル-4-ピラゾールカルボキサミド、N-[[4'-(2-プロピルオキシ)-1,1-ジメチル]フェナシル]-3-トリフルオロメチル-2-ピリジンカルボキサミド、N-[[4'-(2-プロピルオキシ)-1,1-ジメチル]フェナシル]-3-メチル-2-チオフェンカルボキサミド、N-[[4'-(2-プロピルオキシ)-1,1-ジメチル]フェナシル]-1-メチル-3-トリフルオロメチル-4-ピラゾールカルボキサミド、N-[[2'-メチル-4'-(2-ペンチルオキシ)-1,1-ジメチル]フェナシル]-3-トリフルオロメチル-2-ピリジンカルボキサミド、N-[[4'-(2-ペンチルオキシ)-1,1-ジメチル]フェナシル]-3-トリフルオロメチル-2-ピリジンカルボキサミド、フェリムゾン(ferimzone)、スピロキサミン(spiroxamine)、S-2188(fenpyrazamine)、S-2200、ZF-9646、BCF-051、BCM-061、BCM-062等が挙げられる。
In the above-mentioned other agricultural chemicals, as an active ingredient compound of a bactericidal agent, that is, a bactericidal compound (generic name; including partial application, or Japan Plant Protection Association test code), for example, mepanipyrim, pyrimethanil (pyrimethanil) ), Anilinopyrimidine compounds such as cyprodinil, ferimzone;
Tria such as 5-chloro-7- (4-methylpiperidin-1-yl) -6- (2,4,6-trifluorophenyl) [1,2,4] triazolo [1,5-a] pyrimidine Zolopyrimidine compounds;
Pyridinamine compounds such as fluazinam;
Triadimefon, bitertanol, triflumizole, etaconazole, propiconazole, penconazole, flusilazole, microbutanil, cyproconazole cyproconazole), tebuconazole, hexaconazole, furconazole-cis, prochloraz, metconazole, epoxiconazole, tetraconazole, o Oxpoconazole fumarate, sipconazole, prothioconazole, triadimenol, flutriafol, difenoconazole , Fluquinconazole, fenbuconazole, bromuconazole, diniconazole, tricyclazole, probenazole, cimeconazole, pefurazoate, ipconazole, ipconazole ), Azole compounds such as imibenconazole;
Quinoxaline compounds such as quinomethionate;
Dithiocarbamate compounds such as maneb, zineb, mancozeb, polycarbamate, metiram, propineb, thiram;
Organochlorine compounds such as fthalide, chlorothalonil, quintozene;
Imidazole compounds such as benomyl, thiophanate-methyl, carbendazim, thiabendazole, fuberiazole;
Cyanoacetamide compounds such as cymoxanil;
Metalaxyl, metalaxyl-M, mefenoxam, oxadixyl, offurace, benalaxyl, benalaxyl-M, also known as kiralaxyl, chiax ), Fluralaxyl, cyprofuram, carboxin, oxycarboxin, thifluzamide, boscalid, bixafen, isothianil, tiadinil, Anilide compounds such as sedaxane;
Sulfamide-type compounds such as dichlofluanid;
Copper-based compounds such as cupric hydroxide and oxine copper;
Isoxazole compounds such as hymexazol;
Fosetyl aluminum (fosetyl-Al), tolclofos-Methyl, S-benzyl O, O-diisopropyl phosphorothioate, O-ethyl S, S-diphenyl phosphorodithioate, aluminum ethyl hydrogen phosphonate, edifenphos, iprobenphos Organophosphorus compounds such as (iprobenfos);
Phthalimide compounds such as captan, captafol, folpet;
Dicarboximide compounds such as procymidone, iprodione, vinclozolin;
Benzanilide compounds such as flutolanil and mepronil;
Penthiopyrad, 3- (difluoromethyl) -1-methyl-N-[(1RS, 4SR, 9RS) -1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalen-5-yl ] Pyrazole-4-carboxamide and 3- (difluoromethyl) -1-methyl-N-[(1RS, 4SR, 9SR) -1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalene-5 Amide compounds such as -yl] pyrazole-4-carboxamide mixtures (isopyrazam), silthiopham, fenoxanil, furametpyr;
Benzamide compounds such as fluopyram and zoxamide;
Piperazine compounds such as triforine;
Pyridine compounds such as flonicamid and pyrifenox;
Carbinol compounds such as fenarimol;
Piperidine compounds such as fenpropidin;
Morpholine compounds such as fenpropimorph and tridemorph;
Organotin compounds such as fentin hydroxide and fentin acetate;
Urea-based compounds such as pencycuron;
Synamic acid compounds such as dimethomorph, flumorph;
Phenyl carbamate compounds such as dietofencarb;
Cyanopyrrole compounds such as fludioxonil and fenpiclonil;
Azoxystrobin, kresoxim-methyl, metominostrobin, trifloxystrobin, picoxystrobin, oryzastrobin, dimoxystrobin ( strobilurin compounds such as dimoxystrobin), pyraclostrobin, fluoxastrobin;
Oxazolidinone compounds such as famoxadone;
Thiazole carboxamide compounds such as ethaboxam;
Valinamide compounds such as iprovalicarb, benchthiavalicarb-isopropyl;
Acylamino acid compounds such as methyl N- (isopropoxycarbonyl) -L-valyl- (3RS) -3- (4-chlorophenyl) -β-valaniphenate;
Imidazolinone compounds such as fenamidone;
Hydroxyanilide compounds such as fenhexamid;
Benzenesulfonamide compounds such as flusulfamide;
Oxime ether compounds such as cyflufenamid;
Atraquinone compounds;
Crotonic acid compounds;
Antibiotics such as validamycin, kasugamycin, polyoxins;
Guanidine compounds such as iminoctadine and dodine;
Quinoline compounds such as 6-tertiarybutyl-8-fluoro-2,3-dimethylquinolin-4-yl acetate (tebufloquin);
Thiazolidines such as (Z) -2- (2-fluoro-5- (trifluoromethyl) phenylthio) -2- (3- (2-methoxyphenyl) thiazolidine-2-ylidene) acetonitrile (flutianil) Compound;
Other compounds include pyribencarb, isoprothiolane, pyroquilon, diclomezine, quinoxyfen, propamocarb hydrochloride, chloropicrin, dazomet, and sodium metam Metam-sodium, nicobifen, metrafenone, UBF-307, diclocymet, proquinazid, amisulbrom (aka amibromdole), 3- (2,3,4 -Trimethoxy-6-methylbenzoyl) -5-chloro-2-methoxy-4-methylpyridine, 4- (2,3,4-trimethoxy-6-methylbenzoyl) -2,5-dichloro-3-trifluoromethyl Pyridine, pyriofenone, mandipropamid, fluopico Fluopicolide, carpropamid, meptyldinocap, N-[(3 ', 4'-dichloro-1,1-dimethyl) phenacyl] -3-trifluoromethyl-2-pyridinecarboxamide, N-[(3 ', 4'-dichloro-1,1-dimethyl) phenacyl] -3-methyl-2-thiophenecarboxamide, N-[(3', 4'-dichloro-1,1-dimethyl) phenacyl] -1-methyl-3-trifluoromethyl-4-pyrazolecarboxamide, N-[[2'-methyl-4 '-(2-propyloxy) -1,1-dimethyl] phenacyl] -3-trifluoromethyl- 2-pyridinecarboxamide, N-[[2'-methyl-4 '-(2-propyloxy) -1,1-dimethyl] phenacyl] -3-methyl-2-thiophenecarboxamide, N-[[2'-methyl -4 '-(2-propyloxy) -1,1-dimethyl] phenacyl] -1-methyl-3-trifluoromethyl-4-pyrazolecarboxamide, N-[[4'-(2-propyloxy) -1 , 1-dimethyl] fe Nacyl] -3-trifluoromethyl-2-pyridinecarboxamide, N-[[4 '-(2-propyloxy) -1,1-dimethyl] phenacyl] -3-methyl-2-thiophenecarboxamide, N-[[ 4 '-(2-propyloxy) -1,1-dimethyl] phenacyl] -1-methyl-3-trifluoromethyl-4-pyrazolecarboxamide, N-[[2'-methyl-4'-(2-pentyl) Oxy) -1,1-dimethyl] phenacyl] -3-trifluoromethyl-2-pyridinecarboxamide, N-[[4 '-(2-pentyloxy) -1,1-dimethyl] phenacyl] -3-trifluoro Examples thereof include methyl-2-pyridinecarboxamide, ferimzone, spiroxamine, S-2188 (fenpyrazamine), S-2200, ZF-9646, BCF-051, BCM-061, and BCM-062.
 本発明において、フロニカミドの処理量は、対象作物、処理方法、製剤形態等の条件によって異なるので、一概に規定しがたいが、通常、0.1~24,000g/haである。散布処理の場合、通常、フロニカミドの処理量は0.1~10,000g/haであり、望ましくは1~1,000g/haであり、さらに望ましくは10~500g/haであり、その上さらに望ましくは25~500g/haである。水面処理の場合、通常、フロニカミドの処理量は5~1,000g/haであり、望ましくは10~1,000g/haであり、さらに望ましくは50~600g/haである。育苗箱処理の場合、通常、フロニカミドの処理量は0.001~100g/箱であり、望ましくは0.01~10g/箱であり、さらに望ましくは0.1~5g/箱である。
 フロニカミドの有効濃度としては、0.05~7,000ppmであり、望ましくは0.5~700ppmであり、より望ましくは0.5~350ppmであり、更に望ましくは0.8~200ppmである。
In the present invention, the amount of flonicamid treated varies depending on the conditions of the target crop, treatment method, formulation form, etc., and is generally difficult to define, but is usually 0.1 to 24,000 g / ha. In the case of spraying treatment, the treatment amount of flonicamid is usually 0.1 to 10,000 g / ha, preferably 1 to 1,000 g / ha, more preferably 10 to 500 g / ha, and further The preferred range is 25 to 500 g / ha. In the case of water surface treatment, the treatment amount of flonicamid is usually 5 to 1,000 g / ha, desirably 10 to 1,000 g / ha, and more desirably 50 to 600 g / ha. In the case of the seedling box treatment, the treatment amount of flonicamid is usually 0.001 to 100 g / box, preferably 0.01 to 10 g / box, and more preferably 0.1 to 5 g / box.
The effective concentration of flonicamid is 0.05 to 7,000 ppm, desirably 0.5 to 700 ppm, more desirably 0.5 to 350 ppm, and still more desirably 0.8 to 200 ppm.
 次に、本発明の望ましい実施形態のいくつかを例示するが、これらにより本発明は限定解釈されるものではない。
(1)フロニカミドを有効成分として含有するイネ寄生吸汁害虫の交尾行動かく乱剤。
(2)該害虫が、ウンカ類及びヨコバイ類からなる群より選ばれる少なくとも1種である、(1)に記載された交尾行動かく乱剤。
(3)該害虫が、ウンカ類である、(1)に記載された交尾行動かく乱剤。
(4)フロニカミドを有効成分として含有するイネ寄生吸汁害虫の交尾行動かく乱剤を処理して、該害虫を防除する方法。
(5)フロニカミドを有効成分として含有するイネ寄生吸汁害虫の交尾行動かく乱剤を処理して、該害虫の交尾行動をかく乱する方法。
(6)さらに該害虫の次世代個体数を抑制する、(5)に記載された方法。
(7)さらに該害虫の次世代個体数を抑制し、イネを該害虫から保護する、(5)に記載された方法。
(8)フロニカミドの有効成分量が0.1~24,000 g/haで処理される、(5)に記載された方法。
(9)該処理が土壌処理である、(5)に記載された方法。
(10)該交尾行動かく乱剤を水田内に処理する、(5)に記載された方法。
(11)該交尾行動かく乱剤を育苗箱内に処理する、(5)に記載された方法。
(12)フロニカミドを水田内に、0.1~10,000g/haの処理量で散布処理して該害虫を防除する、(5)に記載された方法。
(13)フロニカミドを水田内に、5~1,000g/haの処理量で水面処理して該害虫を防除する、(5)に記載された方法。
(14)フロニカミドを育苗箱内に、0.001~100g/箱の処理量で処理して該害虫を防除する、(5)に記載された方法。
(15)(11)に記載の方法に用いる、フロニカミドと難水溶性樹脂とを含有する有害生物防除用組成物。
(16)製剤中でフロニカミドと難水溶性樹脂がマトリックスを形成していることを特徴とする(15)に記載の有害生物防除用組成物。
(17)難水溶性樹脂が、エチレン・アクリル酸共重合体である、(15)~(16)に記載の組成物。
(18)湿潤剤をさらに含有する、(15)~(17)に記載の組成物。
(19)フロニカミドの平均粒子径が1~100μmである、(15)~(17)に記載の組成物。
(20)フロニカミドの平均粒子径が1~100μmである、(18)に記載の組成物。
(21)(15)~(17)又は(19)に記載された組成物が粒剤である、有害生物防除用組成物。
(22)(18)又は(20)に記載された組成物が粒剤である、有害生物防除用組成物。
(23)フロニカミド及びエチレン・アクリル酸共重合体を混合・混練・造粒し、乾燥する工程を有することを特徴とする(21)に記載の組成物の製造方法。
(24)フロニカミド、エチレン・アクリル酸共重合体及び湿潤剤を混合・混練・造粒し、乾燥する工程を有することを特徴とする(22)に記載の組成物の製造方法。
(25)フロニカミドと難水溶性樹脂とを含有する有害生物防除用組成物。
(26)製剤中でフロニカミドと難水溶性樹脂がマトリックスを形成していることを特徴とする(25)に記載の有害生物防除用組成物。
(27)難水溶性樹脂が、エチレン・アクリル酸共重合体である(25)~(26)に記載の組成物。
(28)湿潤剤をさらに含有する(25)~(27)に記載の有害生物防除用組成物。
(29)フロニカミドの平均粒子径が1~100μmである、(25)~(27)に記載の組成物。
(30)フロニカミドの平均粒子径が1~100μmである、(28)に記載の組成物。
(31)(25)~(27)又は(29)に記載の組成物が粒剤である、有害生物防除用組成物。
(32)(28)又は(30)に記載の組成物が粒剤である、有害生物防除用組成物。
(33)フロニカミド及びエチレン・アクリル酸共重合体を混合・混練・造粒し、乾燥する工程を有することを特徴とする(31)に記載の組成物の製造方法。
(34)フロニカミド及びエチレン・アクリル酸共重合体を混合・混練・造粒し、乾燥する工程を有することを特徴とする(32)に記載の組成物の製造方法。
Next, some desirable embodiments of the present invention will be exemplified, but the present invention is not limited thereto.
(1) A mating behavior disturbing agent for a parasitic parasitic insect of rice containing flonicamid as an active ingredient.
(2) The mating behavior disruptor according to (1), wherein the pest is at least one selected from the group consisting of planthoppers and leafhoppers.
(3) The mating behavior disruptor according to (1), wherein the pest is a planthopper.
(4) A method for controlling a copulation behavior disruptor of a rice parasitic sucking pest containing flonicamid as an active ingredient to control the pest.
(5) A method for disturbing the mating behavior of a pest of rice parasitic juice pests containing flonicamid as an active ingredient by treating the agent.
(6) The method described in (5), further suppressing the next-generation population of the pest.
(7) The method described in (5), further suppressing the next-generation population of the pest and protecting rice from the pest.
(8) The method according to (5), wherein the active ingredient amount of flonicamid is treated at 0.1 to 24,000 g / ha.
(9) The method according to (5), wherein the treatment is soil treatment.
(10) The method according to (5), wherein the mating behavior disrupting agent is treated in a paddy field.
(11) The method according to (5), wherein the mating behavior disruptor is treated in a nursery box.
(12) The method according to (5), wherein flonicamid is sprayed in a paddy field at a treatment amount of 0.1 to 10,000 g / ha to control the pests.
(13) The method according to (5), wherein flonicamid is treated with water in a paddy field at a treatment rate of 5 to 1,000 g / ha to control the pests.
(14) The method according to (5), wherein flonicamid is treated in a seedling box at a treatment amount of 0.001 to 100 g / box to control the pests.
(15) A pest control composition containing flonicamid and a poorly water-soluble resin used in the method according to (11).
(16) The pest control composition as described in (15), wherein flonicamid and a poorly water-soluble resin form a matrix in the preparation.
(17) The composition according to (15) to (16), wherein the poorly water-soluble resin is an ethylene / acrylic acid copolymer.
(18) The composition according to any one of (15) to (17), further comprising a wetting agent.
(19) The composition according to (15) to (17), wherein the average particle size of flonicamid is 1 to 100 μm.
(20) The composition according to (18), wherein the average particle size of flonicamid is 1 to 100 μm.
(21) A composition for controlling pests, wherein the composition described in (15) to (17) or (19) is a granule.
(22) A composition for controlling pests, wherein the composition described in (18) or (20) is a granule.
(23) The method for producing a composition according to (21), comprising a step of mixing, kneading, granulating and drying flonicamid and an ethylene / acrylic acid copolymer.
(24) The method for producing a composition according to (22), comprising a step of mixing, kneading, granulating and drying flonicamid, an ethylene / acrylic acid copolymer, and a wetting agent.
(25) A pest control composition comprising flonicamid and a poorly water-soluble resin.
(26) The pest control composition as described in (25), wherein flonicamid and a poorly water-soluble resin form a matrix in the preparation.
(27) The composition according to any one of (25) to (26), wherein the poorly water-soluble resin is an ethylene / acrylic acid copolymer.
(28) The composition for controlling pests according to (25) to (27), further comprising a wetting agent.
(29) The composition according to any one of (25) to (27), wherein the flonicamid has an average particle size of 1 to 100 μm.
(30) The composition according to (28), wherein the flonicamid has an average particle size of 1 to 100 μm.
(31) A composition for controlling pests, wherein the composition according to (25) to (27) or (29) is a granule.
(32) A composition for controlling pests, wherein the composition according to (28) or (30) is a granule.
(33) The method for producing a composition as described in (31), comprising a step of mixing, kneading, granulating and drying flonicamid and an ethylene / acrylic acid copolymer.
(34) The method for producing a composition as described in (32), comprising a step of mixing, kneading, granulating and drying flonicamid and an ethylene / acrylic acid copolymer.
 以下に、本発明の実施例を記載するが、これらにより本発明は限定解釈されるものではない。
製剤例1
 フロニカミド1重量部、ベントナイト(豊順工業社製)20重量部、粉末炭酸カルシウム(清水工業社製)76重量部を混合した後、トキサノンGR-31A(ポリカルボン酸塩水溶液、三洋化成工業社製)3重量部、サンエキスC(リグニンスルホン酸カルシウム水溶液、日本製紙ケミカル社製)3重量部と必要量の水を加えて混練し、押し出し造粒機により造粒後、乾燥、整粒して農薬粒剤を得た。
Examples of the present invention will be described below, but the present invention is not construed as being limited thereto.
Formulation Example 1
After mixing 1 part by weight of flonicamid, 20 parts by weight of bentonite (manufactured by Toyoshun Kogyo Co., Ltd.) and 76 parts by weight of powdered calcium carbonate (manufactured by Shimizu Kogyo Co., Ltd.), Toxanone GR-31A (polycarboxylate aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.) ) 3 parts by weight, 3 parts by weight of Sun Extract C (calcium lignin sulfonate, manufactured by Nippon Paper Chemical Co., Ltd.) and the required amount of water are kneaded, granulated by an extrusion granulator, dried and sized. A pesticide granule was obtained.
製剤例2
 フロニカミド2重量部、粉末炭酸カルシウム92.3重量部及びポリオキシエチレンスチリルフェニルエーテルサルフェート(ソルポール5096、東邦化学工業社製)3重量部を混合した後、エチレン・アクリル酸共重合体を27w/w%含む水性エマルション(商品名:HYTEC S-3111(東邦化学工業社製))を10重量部加え、必要量加水し混練、押し出し機により造粒後、乾燥、整粒して農薬粒剤を得た。
Formulation Example 2
After mixing 2 parts by weight of flonicamid, 92.3 parts by weight of powdered calcium carbonate, and 3 parts by weight of polyoxyethylene styryl phenyl ether sulfate (Solpol 5096, manufactured by Toho Chemical Industry Co., Ltd.), an ethylene / acrylic acid copolymer was mixed with 27 w / w. % Aqueous emulsion (trade name: HYTEC S-3111 (manufactured by Toho Chemical Industry Co., Ltd.)), add the required amount, knead, granulate with an extruder, dry and sizing to obtain agrochemical granules It was.
製剤例3
 フロニカミド2重量部、クレー 92.3重量部及びポリオキシエチレンスチリルフェニルエーテルサルフェート(ソルポール5096、東邦化学工業社製)3重量部を混合した後、エチレン・アクリル酸共重合体を27w/w%含む水性エマルション(商品名:HYTEC S-3121(東邦化学工業社製))を10重量部加え、必要量加水し混練、押し出し機により造粒後、乾燥、整粒して農薬粒剤を得る。
Formulation Example 3
After mixing 2 parts by weight of flonicamid, 92.3 parts by weight of clay and 3 parts by weight of polyoxyethylene styryl phenyl ether sulfate (Solpol 5096, manufactured by Toho Chemical Industry Co., Ltd.), 27% w / w ethylene / acrylic acid copolymer is contained. Add 10 parts by weight of an aqueous emulsion (trade name: HYTEC S-3121 (manufactured by Toho Chemical Industry Co., Ltd.)), add the necessary amount, knead, granulate with an extruder, dry and sizing to obtain agrochemical granules.
試験例1 フロニカミド育苗箱処理によるトビイロウンカに対する防除効果
 1.2cm×1.2cmセル苗(3本/株)の株元に1.5mg ai/株の割合で、製剤例1に準じて調製した粒剤を育苗箱に処理した。フロニカミド処理1日後にイネをセルから土壌ごと引き抜き、1ポットに1株ずつ移植し、水深を3cmに保持した。小型温室を2つ用意し、フロニカミド処理・無処理それぞれ24ポットを各小型温室に設置した。移植10、17及び30日後にトビイロウンカ(Nilaparvata lugens)成虫各100頭/温室を放虫した。放虫後、一定期間毎にイネに寄生した、イネ24株あたりの成虫の数及び新たに生まれた次世代の幼虫の数を測定した。結果を第1表及び図1に示す。なお、図1中で、○-○(丸印)はフロニカミド処理区における成幼虫数(頭)を表し、△-△(三角印)は無処理区における成幼虫数(頭)を表す。
Test Example 1 Control effect against brown planthopper by treatment with flonicamid seedling box 1.2 mg × 1.2 cm cell seedlings (3 / strain) at a ratio of 1.5 mg ai / strain, prepared according to Formulation Example 1 The agent was processed in a nursery box. One day after the flonicamid treatment, the rice was extracted from the cell together with the soil, transplanted one strain per pot, and the water depth was maintained at 3 cm. Two small greenhouses were prepared, and 24 pots for flonicamid treatment and no treatment were installed in each small greenhouse. Ten , 17 and 30 days after transplanting, 100 adults of Nilaparvata lugens / greenhouse were released. After the release, the number of adults per 24 rice lines and the number of newly born next-generation larvae that infested rice at regular intervals were measured. The results are shown in Table 1 and FIG. In FIG. 1, ◯-○ (circle) represents the number of adult larvae (head) in the flonicamid-treated group, and Δ-Δ (triangle mark) represents the number of adult larvae (head) in the untreated group.
Figure JPOXMLDOC01-appb-T000001
Figure JPOXMLDOC01-appb-T000001
 第1表及び図1において、無処理の成幼虫数の推移から、イネ移植後29日目が第1世代のピークであり、イネ移植後57日目が第2世代のピークであった。イネ移植後39日目に成幼虫数が減少しているのは、第1世代成虫が産卵した卵が孵化前の状態であると推察できる。また、3回の成虫放飼は、実際の水田において、トビイロウンカが他地域から飛来した場面を想定している。この状況下、フロニカミド処理区では第1世代のピークが見られず、第2世代成幼虫数も大幅に抑制した。 In Table 1 and FIG. 1, from the transition of the number of untreated adult larvae, the 29th day after rice transplantation was the first generation peak, and the 57th day after rice transplantation was the second generation peak. It can be inferred that the number of adult larvae decreased on the 39th day after rice transplantation is the state before the eggs hatched by the first generation adults. In addition, the 3 adult release is assumed to be a situation where the brown planthopper flew from another area in an actual paddy field. Under this circumstance, the peak of the first generation was not observed in the flonicamid-treated group, and the number of second-generation adult larvae was greatly suppressed.
試験例2:トビイロウンカに対する交尾行動かく乱作用
 40mm×40mmの脱脂綿に10粒のイネを播種し、背丈約5cmとなったイネ苗を準備した。イネ苗は有効成分フロニカミド200ppmを含有する水溶液で浸漬処理し、風乾し、ガラスバイアル瓶(内径40mm×高さ75mm;容量50ml)内に入れた。老齢幼虫の時点から1頭飼育した未交尾状態のトビイロウンカ(Nilaparvata lugens)の成虫を薬剤無処理イネ苗で飼育した。羽化後6日目から24時間の間は1頭ずつ浸漬処理イネで飼育した。羽化後7日目に浸漬処理イネ上でオスメス各1頭を一緒にしてから24時間経過した後、オスを取り除き、メスは、その後羽化14日目まで産卵させ、取り除いた。新たに生まれた次世代幼虫の数を浸漬処理イネ苗(フロニカミド処理区)および薬剤無処理イネ苗(無処理区)について対比して、次世代幼虫の発生数を測定した。また、オスメス各1頭を一緒にしたとき2時間観察し、交尾行動の有無を確認した。
 なお、未交尾状態で次世代幼虫の発生が無いことを確認するため、無処理区で未交尾のメスを単独で飼育し、次世代幼虫の発生数を測定した(未交尾区)。結果を第2表に示す。
Test Example 2: Mating behavior disturbing action against a brown planthopper 10 seeds of rice were sown on 40 mm × 40 mm absorbent cotton to prepare a rice seedling having a height of about 5 cm. Rice seedlings were immersed in an aqueous solution containing 200 ppm of the active ingredient flonicamid, air-dried, and placed in a glass vial (inner diameter 40 mm × height 75 mm; capacity 50 ml). An adult non-mating leafhopper ( Nilaparvata lugens ) raised from the age of the old larvae was bred with drug-untreated rice seedlings. From the 6th day after emergence, the animals were bred on immersion-treated rice for 24 hours. On the 7th day after emergence, after 24 hours had passed after each male and female were put together on the soaked rice, the male was removed, and the female was then allowed to lay eggs until the 14th day of emergence. The number of next-generation larvae was measured by comparing the number of newly born next-generation larvae in immersion-treated rice seedlings (flonicamide treated group) and drug-untreated rice seedlings (untreated group). Moreover, when one male and one female were put together, they were observed for 2 hours to confirm the presence or absence of mating behavior.
In order to confirm that no next-generation larvae were generated in an unmated state, an unmated female was bred alone in an untreated group, and the number of next-generation larvae was measured (unmated group). The results are shown in Table 2.
Figure JPOXMLDOC01-appb-T000002
Figure JPOXMLDOC01-appb-T000002
試験例3:ネオニコチノイド系殺虫剤に感受性の低下したトビイロウンカ系統に対する交尾行動かく乱作用
 試験例2のトビイロウンカを、代表的なネオニコチノイド系殺虫剤である一般名イミダクロプリドに対して感受性の低下したトビイロウンカに置き換えて、同様に試験を行い、フロニカミド処理区及び無処理区について対比して、次世代幼虫の発生数を測定した。結果を第3表に示す。
Test Example 3: Mating behavior disruptive effect on a brown planthopper line that is less sensitive to neonicotinoid insecticides The testimony of the planthopper of Test Example 2 is less sensitive to the common name imidacloprid, a typical neonicotinoid insecticide The same test was conducted in place of the brown planthopper, and the number of next-generation larvae was measured in comparison with the flonicamid treated group and the untreated group. The results are shown in Table 3.
Figure JPOXMLDOC01-appb-T000003
Figure JPOXMLDOC01-appb-T000003
試験例4:セジロウンカに対する交尾行動かく乱作用
 試験例2のトビイロウンカを、セジロウンカ(Sogatella furcifera)に置き換えて、同様に試験を行い、フロニカミド処理区及び無処理区について対比して、次世代幼虫の発生数を測定した。結果を第4表に示す。
Test example 4: Disrupting effect of mating behavior on white- spotted plant The white- spotted planthopper in Test example 2 was replaced with a white- spotted planthopper ( Sogatella furcifera ), and the same test was conducted. Was measured. The results are shown in Table 4.
Figure JPOXMLDOC01-appb-T000004
Figure JPOXMLDOC01-appb-T000004
試験例5:ヒメトビウンカに対する交尾行動かく乱作用
 試験例2のトビイロウンカを、ヒメトビウンカ(Laodelphax striatella)に置き換えて、同様に試験を行い、フロニカミド処理区及び無処理区について対比して、次世代幼虫の発生数を測定した。結果を第5表に示す。
Test Example 5: Mating behavior disruption effect on Japanese brown planthopper The Japanese brown planthopper of Test Example 2 was replaced with Japanese brown planthopper ( Laodelphax striatella ), and the same test was carried out. The number of next-generation larvae compared with the flonicamid treated group and the untreated group Was measured. The results are shown in Table 5.
Figure JPOXMLDOC01-appb-T000005
 試験例2~5の結果から、本発明では、様々なウンカ類に対して交尾行動かく乱を起こし、次世代個体数を抑制することが分かる。また、従来、ウンカ類防除剤の主流として使用されてきたイミダクロプリドに感受性が低下しているトビイロウンカに対しても本発明は優れた効果を示すことが分かる。
Figure JPOXMLDOC01-appb-T000005
From the results of Test Examples 2 to 5, it can be seen that, in the present invention, copulation behavior disturbance is caused to various planthoppers and the number of next-generation individuals is suppressed. Moreover, it turns out that this invention shows the outstanding effect also to the brown planthopper which has fallen sensitivity to the imidacloprid conventionally used as the mainstream of the planthopper control agent.
試験例6:トビイロウンカに対する交尾行動かく乱作用
 イネ苗を、有効成分フロニカミド50、12.5、3.1及び0.8ppmを含有する水溶液で処理したこと以外は、試験例2に準じて試験を行った。フロニカミド処理区及び無処理区について対比して次世代幼虫の発生数を測定した結果を、第6表に示す。
Test Example 6: Disturbance of mating behavior against brown planthopper A rice seedling was tested according to Test Example 2 except that it was treated with an aqueous solution containing the active ingredients flonicamid 50, 12.5, 3.1 and 0.8 ppm. It was. Table 6 shows the results of measuring the number of generations of next-generation larvae in comparison with the flonicamid-treated group and the non-treated group.
Figure JPOXMLDOC01-appb-T000006
Figure JPOXMLDOC01-appb-T000006
試験例7:セジロウンカに対する交尾行動かく乱作用
 イネ苗を、有効成分フロニカミド50、12.5及び3.1ppmを含有する水溶液で処理したこと以外は、試験例4に準じて試験を行った。フロニカミド処理区及び無処理区について対比して次世代幼虫の発生数を測定した結果を、第7表に示す。
Test Example 7 Mating Action Disturbing Action on White-Spotted Plant A rice seedling was tested according to Test Example 4 except that it was treated with an aqueous solution containing the active ingredients flonicamid 50, 12.5 and 3.1 ppm. Table 7 shows the results of measuring the number of generations of next-generation larvae in comparison with the flonicamid-treated group and the untreated group.
Figure JPOXMLDOC01-appb-T000007
Figure JPOXMLDOC01-appb-T000007
試験例8:ヒメトビウンカに対する交尾行動かく乱作用
 イネ苗を、有効成分フロニカミド50、12.5及び3.1ppmを含有する水溶液で処理したこと以外は、試験例5に準じて試験を行った。フロニカミド処理区及び無処理区について対比して次世代幼虫の発生数を測定した結果を、第8表に示す。
Test Example 8 Mating Behavior Disturbing Action for Brown Bean Spike A test was conducted according to Test Example 5 except that rice seedlings were treated with an aqueous solution containing the active ingredients flonicamid 50, 12.5, and 3.1 ppm. Table 8 shows the results of measuring the number of generations of next-generation larvae in comparison with the flonicamid-treated group and the non-treated group.
Figure JPOXMLDOC01-appb-T000008
Figure JPOXMLDOC01-appb-T000008
試験例9:ネオニコチノイド系殺虫剤に感受性の低下したトビイロウンカ系統に対する交尾行動かく乱作用
 イネ苗を、有効成分フロニカミド0.8ppmを含有する水溶液で処理したこと以外は、試験例3に準じて試験を行った。フロニカミド処理区及び無処理区について対比して、次世代幼虫の発生数を測定した結果を、第9表に示す。
Test Example 9: Mating behavior disturbing action against a brown planthopper line that is less sensitive to neonicotinoid insecticides Tested according to Test Example 3 except that rice seedlings were treated with an aqueous solution containing 0.8 ppm of the active ingredient flonicamid Went. Table 9 shows the results of measuring the number of generations of next-generation larvae in comparison with the flonicamid-treated group and the non-treated group.
Figure JPOXMLDOC01-appb-T000009
 試験例6~9の結果から、本発明では、様々なウンカ類に対して3.1ppmなどの低濃度の有効成分を処理した場合においても、交尾行動をかく乱し、次世代個体数を抑制することが分かる。また、従来、ウンカ類防除剤の主流として使用されてきたイミダクロプリドに感受性が低下しているトビイロウンカに対しても、本発明は、3.1ppmなどの低濃度の有効成分を処理した場合においても、優れた効果を示すことが分かる。
Figure JPOXMLDOC01-appb-T000009
From the results of Test Examples 6 to 9, in the present invention, even when a low concentration of active ingredient such as 3.1 ppm is treated for various planthoppers, the mating behavior is disturbed and the number of next generation individuals is suppressed. I understand that. In addition, for the brown planthopper whose sensitivity to imidacloprid, which has been conventionally used as the mainstream of the planthopper control agent, even when a low concentration active ingredient such as 3.1 ppm is processed, It can be seen that the effect is excellent.
試験例10:ツマグロヨコバイに対する交尾行動かく乱作用
 試験例2のトビイロウンカを、ツマグロヨコバイ(Nephotettix cincticeps)に置き換えて、同様に試験を行い、イネ苗は有効成分フロニカミド200、50ppmを含有する水溶液で処理したフロニカミド処理区及び無処理区について対比して、次世代幼虫の発生数を測定した。結果を第10表に示す。
Test Example 10: Mating behavior disturbing action against leafhopper leafhopper The leafhopper of Experiment example 2 was replaced with leafhopper leafhopper ( Nephotettix cincticeps ), and the same test was conducted, and rice seedlings were treated with flonicamid treated with an aqueous solution containing the active ingredient flonicamid 200, 50 ppm. The number of next-generation larvae was measured in comparison with the ward and the untreated ward. The results are shown in Table 10.
Figure JPOXMLDOC01-appb-T000010
 試験例10の結果から、本発明では、ツマグロヨコバイに対して次世代個体数を抑制することが分かる。
Figure JPOXMLDOC01-appb-T000010
From the results of Test Example 10, it can be seen that the present invention suppresses the number of next-generation individuals against the leafhopper leafhopper in the present invention.
試験例11 フロニカミド育苗箱処理によるトビイロウンカに対する防除効果
 30cm×60cm育苗箱に6、12、24及び36g ai/箱の割合で、前記製剤例2に準じて調製した有害生物防除用組成物を育苗箱に処理した。無処理区とジノテフラン粒剤(商品名:スタークル箱粒剤、三井化学アグロ社製)処理区(24g ai/箱)及びイミダクロプリド粒剤(商品名:アドマイヤー箱粒剤、バイエルクロップサイエンス社製)処理区(24g ai/箱)を設置した。移植当日処理にフロニカミドを処理し、田植え機により1区32mの圃場に移植した。移植36、43、51、57及び65日後に圃場100mに対してトビイロウンカ成虫各500頭及び卵12000個を放虫した。移植78、89及び96にイネに寄生した、イネ24株あたりの成虫の数及び新たに生まれた次世代の幼虫の数を測定した。結果を第11表に示す。なお、参考として図2に、フロニカミド処理区について、24 g ai/10aフロニカミド処理区の場合を代表してグラフに表す。●-●(黒色丸印)は24 g ai/10aフロニカミド処理区における成幼虫数(頭)を表し、□-□(白色四角印)はイミダクロプリド粒剤処理区における成幼虫数(頭)を表し、△-△(白色三角印)はジノテフラン粒剤処理区における成幼虫数(頭)を表し、×-×(×印)は無処理区における成幼虫数(頭)を表す。
Test Example 11 Control effect against brown planthopper by treatment with flonicamid nursery box A pest control composition prepared according to Formulation Example 2 in a ratio of 6, 12, 24 and 36 g ai / box in a 30 cm × 60 cm nursery box Processed. Untreated zone and dinotefuran granule (trade name: Starkle box granule, manufactured by Mitsui Chemicals Agro) Treatment zone (24 g ai / box) and imidacloprid granule (trade name: Admeier box granule, manufactured by Bayer CropScience) A treatment zone (24 g ai / box) was installed. Flonicamide was treated on the day of transplantation, and transplanted to a field of 32 m 2 in 1 ward by a rice planting machine. 36, 43, 51, 57, and 65 days after transplantation, 500 adults of brown planthopper and 12,000 eggs were released on 100 m 2 of the field. The number of adults per 24 strains of rice and the number of newly born next-generation larvae infested with rice in transplants 78, 89 and 96 were measured. The results are shown in Table 11. For reference, FIG. 2 shows a graph of the flonicamid-treated section as a representative example of the 24 g ai / 10a flonicamid-treated section. ●-● (black circle) represents the number of adult larvae (head) in the 24 g ai / 10a flonicamid-treated group, and □-□ (white square mark) represents the number of adult larvae in the imidacloprid granule-treated group (head). .DELTA .-. DELTA. (White triangles) represent the number of adult larvae (head) in the dinotefuran granule-treated group, and xx (x mark) represents the number of adult larvae (head) in the untreated group.
Figure JPOXMLDOC01-appb-T000011
Figure JPOXMLDOC01-appb-T000011
 5回の放虫は、西南暖地の水田において、トビイロウンカが他地域から飛来する時期に合わせて実施した。無処理の成幼虫数の推移から、イネ移植後89日目が第1世代(次世代)のピークであった。対照剤スタークル箱粒剤処理区では調査開始の移植70日後まで寄生成幼虫密度を抑制していたが、その後増加に転じた。対照剤アドマイヤー箱粒剤処理区でも同様に調査開始の移植70日後まで寄生成幼虫密度を抑制していたが、その後増加に転じ、移植後89日目が第1世代(次世代)のピークが観察された。この状況下、フロニカミド処理区では第1世代(次世代)のピークが見られず、移植89日後まで寄生成幼虫数を大幅に抑制した。この結果は、本発明が、害虫個体数の増加を薬剤処理後可能な限り長い間抑制したいという要求があるイネ寄生吸汁害虫防除の場面において、特に有用であることを示している。 5 times of insect release were carried out in paddy fields in the southwestern warm districts when the brown planthopper flew from other areas. From the transition of the number of untreated adult larvae, the first generation (next generation) peak was on the 89th day after rice transplantation. In the control agent Starkle granule treatment group, the density of the formed larvae was suppressed until 70 days after transplantation after the start of the investigation, but thereafter it started to increase. Similarly, in the control agent Admeier box granule treatment group, the density of the formed larvae was suppressed until 70 days after the transplantation, which started the investigation. However, the density started to increase, and the first generation (next generation) peak occurred on the 89th day after the transplantation. Was observed. Under this circumstance, the peak of the first generation (next generation) was not observed in the flonicamid treatment group, and the number of formed larvae was significantly suppressed until 89 days after transplantation. This result shows that the present invention is particularly useful in the situation of controlling rice parasitic sap pests where there is a demand to suppress the increase in the number of insect pests as long as possible after the chemical treatment.
試験例12 フロニカミド茎葉処理によるトビイロウンカに対する防除効果
 田植え機により1区32mの圃場に移植した。移植36、43、51、57及び65日後に圃場100mに対してトビイロウンカ成虫各500頭及び卵12000個を放虫した。移植70日後、出穂期にフロニカミドを150L/10aの散布水量で茎葉処理した。無処理区とピメトロジン水和剤(商品名:チェス水和剤、シンジェンタ社製)処理区及びジノテフラン水溶剤(商品名:スタークル顆粒水溶剤、三井化学アグロ社製)処理区を設置した。処理直前、処理2、8、19、26及び33日後にイネに寄生した、イネ24株あたりの成虫の数及び新たに生まれた次世代の幼虫の数を測定した。結果を第12表に示す。
Test Example 12 Control effect against brown planthopper by treatment with flonicamid stalks and leaves The plant was transplanted to a field of 32 m 2 in 1 ward by a rice planting machine. 36, 43, 51, 57, and 65 days after transplantation, 500 adults of brown planthopper and 12,000 eggs were released on 100 m 2 of the field. 70 days after transplantation, flonicamid was treated with foliacamide at a heading period with a spraying amount of 150 L / 10a. An untreated zone, a pymetrozine wettable powder (trade name: Chess wettable powder, manufactured by Syngenta) treatment zone and a dinotefuran aqueous solvent (trade name: Starkle granule aqueous solvent, manufactured by Mitsui Chemicals Agro Co., Ltd.) treatment zone were installed. Immediately before treatment, the number of adult worms per 24 strains of rice and the number of newly born next-generation larvae infested with rice after 2, 8, 19, 26 and 33 days of treatment were measured. The results are shown in Table 12.
Figure JPOXMLDOC01-appb-T000012
Figure JPOXMLDOC01-appb-T000012
 5回の放虫は、西南暖地の水田において、トビイロウンカが他地域から飛来する時期に合わせて実施した。無処理の成幼虫数の推移から、処理19日目が第1世代(次世代)のピークであった。処理26日目に成幼虫数が減少しているのは、第1世代成虫が産卵した卵が孵化前の状態であると推察できる。対照剤ピメトロジン水和剤及びジノテフラン水溶剤処理区では共に高い密度抑制効果を示した。この状況下、フロニカミド処理区では第1世代(次世代)のピークが見られず、処理2~3週間後まで対照剤と同等に寄生成幼虫数を抑制した。 5 times of insect release were carried out in paddy fields in the southwestern warm districts when the brown planthopper flew from other areas. From the transition of the number of untreated adult larvae, the 19th day of treatment was the peak of the first generation (next generation). It can be inferred that the number of adult larvae decreased on the 26th day of treatment is the state before the eggs hatched by the first generation adults. Both the control agent, pymetrozine wettable powder and dinotefuran aqueous solvent treatment group showed a high density suppressing effect. Under this circumstance, the first generation (next generation) peak was not observed in the flonicamid-treated group, and the number of formed larvae was suppressed to the same level as the control agent until 2 to 3 weeks after the treatment.
 本発明は、稲作分野において主要な害虫とされている吸汁害虫であるウンカ類の防除に利用することができる。
 なお、2010年7月29日に出願された日本特許出願2010-170936号の明細書、特許請求の範囲、図面及び要約書の全内容をここに引用し、本発明の明細書の開示として、取り入れるものである。
INDUSTRIAL APPLICABILITY The present invention can be used for controlling planthoppers that are sucking pests that are regarded as major pests in the field of rice cultivation.
It should be noted that the entire contents of the specification, claims, drawings and abstract of Japanese Patent Application 2010-170936 filed on July 29, 2010 are cited herein as disclosure of the specification of the present invention. Incorporated.

Claims (19)

  1.  フロニカミドを有効成分として含有するイネ寄生吸汁害虫の交尾行動かく乱剤。 Mating behavior disturbing agent for parasitic parasitic insects of rice containing flonicamid as an active ingredient.
  2.  該害虫が、ウンカ類である、請求項1に記載された交尾行動かく乱剤。 The mating behavior disruptor according to claim 1, wherein the pest is a planthopper.
  3.  フロニカミドを有効成分として含有するイネ寄生吸汁害虫の交尾行動かく乱剤を処理して、該害虫を防除する方法。 A method of controlling a pest by treating a mating behavior disturbing agent of a parasitic rice soup pest containing flonicamid as an active ingredient.
  4.  フロニカミドを有効成分として含有するイネ寄生吸汁害虫の交尾行動かく乱剤を処理して、該害虫の交尾行動をかく乱する方法。 A method of disrupting the mating behavior of a pest of rice parasitic sucking pests containing flonicamid as an active ingredient to treat the mating behavior of the pests.
  5. さらに該害虫の次世代個体数を抑制する、請求項4に記載された方法。 Furthermore, the method described in Claim 4 which suppresses the next-generation population of this pest.
  6.  さらに該害虫の次世代個体数を抑制し、イネを該害虫から保護する、請求項4に記載された方法。 The method according to claim 4, further comprising suppressing the next-generation population of the pest and protecting rice from the pest.
  7.  フロニカミドの有効成分量が0.1~24,000 g/haで処理される、請求項4に記載された方法。 The method according to claim 4, wherein the active ingredient amount of flonicamid is treated at 0.1 to 24,000 g / ha.
  8.  該処理が土壌処理である、請求項4に記載された方法。 The method according to claim 4, wherein the treatment is a soil treatment.
  9.  該交尾行動かく乱剤を育苗箱内に処理する、請求項4に記載された方法。 The method according to claim 4, wherein the mating behavior disrupting agent is treated in a nursery box.
  10.  請求項9に記載の方法に用いる、フロニカミドと難水溶性樹脂とを含有する有害生物防除用組成物。 A pest control composition containing flonicamid and a poorly water-soluble resin used in the method according to claim 9.
  11.  難水溶性樹脂が、エチレン・アクリル酸共重合体である請求項10に記載の組成物。 The composition according to claim 10, wherein the poorly water-soluble resin is an ethylene / acrylic acid copolymer.
  12.  湿潤剤をさらに含有する、請求項10に記載の組成物。 The composition according to claim 10, further comprising a wetting agent.
  13.  湿潤剤が、ポリオキシエチレンスチリルフェニルエーテルサルフェートである請求項12に記載の組成物。 The composition according to claim 12, wherein the wetting agent is polyoxyethylene styryl phenyl ether sulfate.
  14.  フロニカミドの平均粒子径が1~100μmである請求項10に記載の組成物。 The composition according to claim 10, wherein flonicamid has an average particle size of 1 to 100 µm.
  15.  請求項10に記載の組成物が、粒剤である、有害生物防除用組成物。 A composition for controlling pests, wherein the composition according to claim 10 is a granule.
  16.  フロニカミド及びエチレン・アクリル酸共重合体を混合・混練・造粒し、乾燥する工程を有することを特徴とする請求項15に記載の組成物の製造方法。 The method for producing a composition according to claim 15, comprising a step of mixing, kneading, granulating and drying flonicamid and an ethylene / acrylic acid copolymer.
  17.  フロニカミドと難水溶性樹脂とを含有する有害生物防除用組成物。 A composition for controlling pests containing flonicamid and a poorly water-soluble resin.
  18.  湿潤剤をさらに含有する、請求項17に記載の有害生物防除用組成物。 The composition for controlling pests according to claim 17, further comprising a wetting agent.
  19.  請求項18に記載の組成物が粒剤である、有害生物防除用組成物。 A composition for controlling pests, wherein the composition according to claim 18 is a granule.
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