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WO2019142044A1 - Novel agrochemical combinations - Google Patents

Novel agrochemical combinations Download PDF

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Publication number
WO2019142044A1
WO2019142044A1 PCT/IB2018/060686 IB2018060686W WO2019142044A1 WO 2019142044 A1 WO2019142044 A1 WO 2019142044A1 IB 2018060686 W IB2018060686 W IB 2018060686W WO 2019142044 A1 WO2019142044 A1 WO 2019142044A1
Authority
WO
WIPO (PCT)
Prior art keywords
fungicide
spp
fipronil
azoxystrobin
combination
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/IB2018/060686
Other languages
French (fr)
Inventor
Seara WAGNER
Gilson Aparecido Hermenegildo OLIVEIRA
Sambandam Panchatsharam VAIDYALINGAM
Mahesh Dharma BORANE
Ana Flávia QUEIROZ
Natalia GONÇALVES
Shailendra Mitharam Bharambe
Pradip Dattatray WAGH
Jaidev Rajnikant Shroff
Vikram Rajnikant Shroff
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
UPL Ltd
Original Assignee
UPL Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by UPL Ltd filed Critical UPL Ltd
Priority to PE2020000937A priority Critical patent/PE20200934A1/en
Priority to MX2020007450A priority patent/MX2020007450A/en
Priority to CU2020000049A priority patent/CU24634B1/en
Publication of WO2019142044A1 publication Critical patent/WO2019142044A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • 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
    • A01N51/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/34Nitriles
    • 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
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/34Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
    • 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
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/40Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
    • 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
    • A01N59/00Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/16Heavy metals; Compounds thereof
    • A01N59/20Copper
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/541,3-Diazines; Hydrogenated 1,3-diazines
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/02Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
    • 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
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/12Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
    • A01N47/14Di-thio analogues thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/18Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring

Definitions

  • the present invention relates to agrochemical combinations for the control of plant pests. More particularly, the present invention relates to novel combinations, compositions comprising these combinations and methods of using the combinations for the treatment of plant propagation material.
  • Combination of insecticides and fungicides are used to broaden the spectrum of control of insect and fungal pests, reduce dosage, thereby reducing environmental impact, and decrease chances of development of resistance.
  • the combination of insecticides and fungicides at times demonstrate an additive or synergistic effect that results in an improved control on the pests.
  • one object of the present invention is to provide improved combinations of insecticides and fungicides for the control of soil borne pests.
  • Another object of the present invention is to provide a method and a composition for controlling insect pests and fungal diseases around plant propagation material.
  • Yet another object of the present invention is to provide improved combinations of insecticides and fungicides that promote plant health.
  • Embodiment of the present invention can ameliorate one or more of the above mentioned problems.
  • an aspect of the present invention can provide combinations of fipronil; azoxystrobin; at least one benzimidazole fungicide; and either a multi-site fungicide or a neonicotinoid insecticide.
  • Another aspect of the present invention can provide a method of improving yield in crops, the method comprising applying, to a plant propagation material of said crop, a combination comprising fipronil, azoxystrobin, at least one benzimidazole fungicide and either a multi-site fungicide or a neonicotinoid insecticide.
  • Yet another aspect of the present invention can provide a method of improving plant health, the method comprising applying, to a plant propagation material of said crop, a combination comprising fipronil, azoxystrobin, a benzimidazole fungicide and either a multi-site fungicide or a neonicotinoid insecticide.
  • Another aspect of the present invention can provide a composition for treating plant propagation material, the composition comprising fipronil, azoxystrobin, at least one benzimidazole fungicide and either a multi-site fungicide or a neonicotinoid insecticide.
  • the present invention can provide a method of controlling pests by treating a plant propagation material with a composition comprising fipronil, azoxystrobin, at least one benzimidazole fungicide and either a multi-site fungicide or a neonicotinoid insecticide.
  • the present invention can provide a composition for improving plant health, the method comprising applying to a plant propagation material of said crop, a combination comprising fipronil, azoxystrobin, a benzimidazole fungicide and either a multi-site fungicide or a neonicotinoid insecticide.
  • plant propagation material refers to the parts of the plant, such as seeds, which can be used for the propagation of the plant and vegetative plant material such as cuttings and tubers (for example, potatoes). There may be mentioned, e.g., the seeds (in the strict sense), roots, fruits, tubers, bulbs, rhizomes, parts of plants. Germinated plants or young plants, which may be transplanted after germination or after emergence from the soil.
  • Insecticidal refers to the ability of a substance to increase mortality or inhibit, growth rate of insects.
  • Fungicidal refers to the ability of a substance to decrease or inhibit growth of fungi.
  • insects refers to an amount of an active that kills or inhibits the plant disease for which control is desired, in an amount not significantly toxic to the plant being treated.
  • To“control” or“controlling” insects means to inhibit, through a toxic effect, the ability of insect pests to survive, grow, feed, and/or reproduce, or to limit insect-related damage or loss in crop plants or denotes control and prevention of a disease. Controlling effects include all deviation from natural development, for example: killing, retardation, decrease of the fugal disease or insect pest.
  • To“control” insects may or may not mean killing the insects, although it preferably means killing the insects.
  • the term“agriculturally acceptable amount of active” refers to an amount of an active that kills or inhibits the plant disease for which control is desired, in an amount not significantly toxic to the plant being treated.
  • improved seed vigour refers to seed properties that determines potential for fast and uniform emergence, and development of seedlings under a wide range of field conditions, when compared with the same trait in a control plant which has been grown under the same conditions in the absence of the method of the invention.
  • Such traits may include, early and/or improved germination, improved emergence, increased root growth, a developed root system, increased root nodulation, increased shoot growth, improvement in plant height, an increase in plant weight (fresh or dry), bigger leaf blades, greener leaf colour, increased pigment content, increased photosynthetic activity, earlier flowering, longer panicles, early grain maturity, increased seed, fruit or pod size, increased pod or ear number, increased seed number per pod or ear, increased seed mass, enhanced seed filling, delay of senescence, and improved vitality of the plant.
  • the present inventors found unexpected synergy when fipronil and azoxystrobin was combined with a benzimidazole fungicide and either a multi-site fungicide or a neonicotinoid insecticide. More specifically, the present inventors found unexpected synergy when fipronil and azoxystrobin was combined with either carbendazim or thiophanate methyl and either imidacloprid or a multi-site fungicide or both.
  • Fipronil is a phenylpyrazole insecticide which acts on the insects’ central nervous system by blocking GABA-gated chloride channels and glutamate-gated chloride channels. Its chemical name is (RS)-5-amino-1-[2,6-dichloro-4- (trifluoromethyl)phenyl]-4- (trifluoromethylsulfinyl)-1 H-pyrazole-3-carbonitrile.
  • Azoxystrobin is a systemic fungicide belonging to the strobilurin class of compounds. Its mode of action is bought about by attaching to the Qo site of Complex III of the mitochondrial electron transport chain, thereby preventing production of ATP. Its chemical name is methyl (E)-2- ⁇ 2-[6-(2- cyanophenoxy)pyrimidin-4-yloxy]phenyl ⁇ -3-methoxyacrylate.
  • Benzimidazole fungicides inhibit mitosis and cell division in fungi. They are broad spectrum fungicides that are known to control a wide variety of fungi.
  • Neonicotinoid insecticides are systemic with contact and stomach action. Acetylcholine receptor (nAChR) agonist. These insecticides are known to control a broad spectrum of insect pests.
  • nAChR Acetylcholine receptor
  • Multi-site fungicides are known to attack fungi at multiple sites. These fungicides are used for broad-spectrum disease control.
  • Known multi-site fungicides include but are not limited to dithiocarbamates, phthalimides, chloronitriles, inorganic fungicides, sulfamides, bis-guanidines, triazines, quinones, quinoxalines, dicoarboxamides etc.
  • the present inventors believe that the combination of the present invention surprisingly results in a synergistic action.
  • the combinations of the present invention allow for a broad spectrum of pest control and has surprisingly improved plant vigour and yield.
  • the broad spectrum of the present combination also provides a solution for preventing the development of resistance.
  • an aspect of the present invention can provide combinations comprising:
  • At least one active agent selected from a neonicotinoid insecticide or a multi-site fungicide or both.
  • the benzimidazole fungicide is selected from at least one of albendazole, benomyl, carbendazim, chlorfenazole, cypendazole, debacarb, fuberidazole, mecarbinzid, rabenzazole, thiabendazole, furophanate, thiophanate, thiophanate-methyl.
  • the benzimidazole fungicide is selected from benomyl, carbendazim and thiophanate or thiophanate-methyl.
  • the benzimidazole fungicide is carbendazim.
  • the benzimidazole fungicide is thiophanate methyl.
  • the multi-site fungicide is a fungicide selected from the group consisting of dithiocarbamates, phthalimides, chloronitriles, inorganic fungicides, sulfamides, bis-guanidines, triazines, quinones, quinoxalines, and di carboxamides.
  • the dithiocarbamate fungicide is selected from asamobam, asomate, azithiram, carbamorph, cufraneb, cuprobam, disulfiram, ferbam, metam, nabam, tecoram, thiram, urbacide, ziram, dazomet, etem, milneb, mancopper, mancozeb, maneb, metiram, polycarbamate, propineb and zineb.
  • the dithiocarbamate fungicide is selected from maneb, mancozeb and zineb.
  • the dithiocarbamate fungicide is mancozeb.
  • the multi-site fungicide is a phthalimide fungicide selected from captan, captafol and folpet.
  • the multi-site fungicide is a chloronitrile fungicide such as chlorothalonil. In an embodiment, the multi-site fungicide is a sulfamide fungicide selected from dichlofluanid and tolylfluanid.
  • the multi-site fungicide is a bis-guanidine fungicide selected from guazatine and iminoctadine.
  • the multi-site fungicide is a triazine fungicide selected from anilazine. In an embodiment, the multi-site fungicide is a quinone fungicide dithianon.
  • the multi-site fungicide is a quinoxaline fungicide selected from quinomethionate and chlorquinox. In an embodiment, the multi-site fungicide is a dicarboxamide fungicide selected from fluoroimide.
  • the multi-site fungicide is an inorganic fungicide selected from copper fungicides including copper (II) hydroxide, copper oxychloride, copper (II) sulfate, basic copper sulfate, Bordeaux mixture, copper salicylate C7H 4 03*Cu, cuprous oxide CU2O; or sulphur.
  • copper fungicides including copper (II) hydroxide, copper oxychloride, copper (II) sulfate, basic copper sulfate, Bordeaux mixture, copper salicylate C7H 4 03*Cu, cuprous oxide CU2O; or sulphur.
  • the neonicotinoid insecticide may be selected from the group consisting of acetamiprid, clothianidin, imidacloprid, nitenpyram, nithiazine, thiacloprid and thiamethoxam.
  • the neonicotinoid insecticide is selected from the group consisting of acetamiprid, thiamethoxam and imidacloprid.
  • an embodiment of the present invention can provide combinations for treatment of plant propagation material comprising:
  • a benzimidazole fungicide selected from carbendazim or thiophanate- methyl
  • At least one active agent selected from imidacloprid, acetamiprid, thiamethoxam, mancozeb, maneb, zineb, folpet, chlorothalonil, and tribasic copper sulfate.
  • a benzimidazole fungicide selected from carbendazim or thiophanate methyl
  • a benzimidazole fungicide selected from carbendazim or thiophanate methyl
  • Another embodiment of the present invention may provide combinations comprising: i) fipronil;
  • a benzimidazole fungicide selected from carbendazim or thiophanate- methyl
  • azoxystrobin iii) azoxystrobin; iii) a benzimidazole fungicide selected from carbendazim or thiophanate- methyl; and
  • a benzimidazole fungicide selected from carbendazim or thiophanate- methyl
  • a benzimidazole fungicide selected from carbendazim or thiophanate- methyl
  • the constituent fungicides of the combination of the present invention may be admixed in ratio of (1-80): (1-80): (1-80): (1-80) of the fipronil, azoxystrobin, benzimidazole fungicide, neonicotinoid or multi-site fungicide respectively.
  • the combinations of the present invention may be admixed with suitable agrochemical adjuvants to form compositions.
  • an aspect of the present invention may provide a seed treatment composition comprising:
  • azoxystrobin iii) azoxystrobin; iii) a benzimidazole fungicide selected from carbendazim or thiophanate methyl;
  • an active selected from neonicotinoid or a multi-site fungicide or both;
  • Another aspect of the present invention may provide a seed treatment composition comprising:
  • a benzimidazole fungicide selected from carbendazim or thiophanate methyl
  • At least one active agent selected from imidacloprid, acetamiprid, thiamethoxam, mancozeb, maneb, zineb, folpet, chlorothalonil, and tribasic copper sulfate; and
  • the total amount of fipronil in the composition may typically be in the range of 0.1 to 99% by weight, preferably 0.2 to 90% by weight.
  • the total amount of azoxystrobin in the composition may be in the range of 0.1 to 99% by weight.
  • the total amount of benzimdazole inhibitor in the composition may be in the range of 0.1 to 99% by weight.
  • the total amount of neonicotinoid in the composition may be in the range of 0.1 to 99% by weight or the total amount of multi-site fungicide in the composition may be in the range of 0.1 to 99% by weight.
  • the constituent fungicides and insecticides of the composition of the present invention may be admixed in ratio of (1-80): (1-80): (1-80): (1-80) of the fipronil, azoxystrobin, benzimidazole fungicide and either neonicotinoid or multi-site fungicide respectively.
  • the constituents of the composition of the present invention may be applied as per known methods of application to seeds and other plant propagation material or transplanted saplings.
  • the compositions can be formulated into either solid or liquid formulations that are suitable for application to plant propagation material.
  • the formulation may be made as known formulation types such as wettable powders (WP), solutions (LS), emulsions (ES), suspension concentrates (FS), water dispersible granule (WG), or aqueous suspension concentrate (CS).
  • the formulation may be applied by various methods such methods using conventional treating techniques and machines, such as fluidized bed techniques, the roller mill method, rotostatic seed treaters, and drum coaters, spouted beds etc.
  • Pre and post coating procedures such as sizing etc., may also be carried out. Such procedures are known in the art. It is readily understood that plant propagation material will be treated only once it is removed from the plant and is ready to be re-sown. In an embodiment, the treatment may occur before sowing of the plant propagation material so that the sown material has been pre-treated with the combination.
  • seed coating or seed pelleting are preferred in the treatment of the combinations according to the invention. As a result of the treatment, the active ingredients in the combination are adhered on to the seed and therefore available for pest and/or disease control.
  • the formulations may contain standard agriculturally acceptable adjuvants, carriers, diluents, emulsifiers, fillers, anti-foaming agents, thickening agents, anti freezing agents, biocides, pigments etc.
  • Suitable agricultural adjuvants and carriers may include, but are not limited to, crop oil concentrates; methylated seed oils, emulsified methylated seed oil, nonylphenol ethoxylate; benzylcocoalkyldimethyl quaternary ammonium salt; blend of petroleum hydrocarbon, alkyl esters, organic acid, and anionic surfactant; C9-C11 alkylpolyglycoside; phosphated alcohol ethoxylate; natural primary alcohol (C12- C16) ethoxylate; di-sec-butylphenol EO-PO block copolymer; polysiloxane-methyl cap; nonylphenol ethoxylate, urea ammonium nitrate; tridecyl alcohol (synthetic) ethoxylate (8EO); tallow amine ethoxylate ; PEG(400) dioleate-99, alkyl sulfates, such as diethanolammonium lauryl sulfate; al
  • Suitable liquid carriers that may be employed in a composition of the present invention may include water or organic solvents.
  • the organic solvents include, but are not limited to, petroleum fractions or hydrocarbons such as mineral oil, aromatic solvents, paraffinic oils, and the like; vegetable oils such as soybean oil, rapeseed oil, olive oil, castor oil, sunflower seed oil, coconut oil, corn oil, cottonseed oil, linseed oil, palm oil, peanut oil, safflower oil, sesame oil, tung oil and the like; esters of the above vegetable oils; esters of monoalcohols or dihydric, trihydric, or other lower polyalcohols (4-6 hydroxy containing), such as 2-ethyl hexyl stearate, n-butyl oleate, isopropyl myristate, propylene glycol dioleate, di-octyl succinate, di-butyl adipate, di-octyl phthalate and the like; est
  • Organic solvents include, but are not limited to toluene, xylene, petroleum naphtha, crop oil, acetone, methyl ethyl ketone, cyclohexanone, trichloroethylene, perchloroethylene, ethyl acetate, amyl acetate, butyl acetate, propylene glycol monomethyl ether and diethylene glycol monomethyl ether, methyl alcohol, ethyl alcohol, isopropyl alcohol, amyl alcohol, ethylene glycol, propylene glycol, glycerine, N-methyl-2-pyrrolidinone, N,N-dimethyl alkylamides, dimethyl sulfoxide.
  • Solid carriers that may be employed in the compositions of the present invention may include but are not limited to attapulgite, pyrophyllite clay, silica, kaolin clay, kieselguhr, chalk, diatomaceous earth, lime, calcium carbonate, bentonite clay, Fuller's earth, talc, cottonseed hulls, wheat flour, soybean flour, pumice, wood flour, walnut shell flour, lignin, cellulose etc.
  • Thickeners such as silicates such as meal silicates, sodium carboxymethyl cellulose, methyl cellulose, ethyl cellulose, polyvinylalcohol, sodium alginate, Sodium poly acrylate, xanthan gum, welan gum, gum arabic, montmorillonite, lignosulfonates, hydroxy methyl cellulose, dextrin, starch and mixtures thereof;
  • Anti-freezing agents such as glycerin, ethylene glycol, propylene glycol, preferably propylene glycol and the like.
  • Anti-foaming agents such as silicone oils, mineral oils, Fatty acid ester; biocides such as sodium benzoate, 1 ,2-benzisothiazoline - 3-one, 2-methyl-4-isothiazolin-3-one, 5-chloro-2-methyl-4-isothiazolin-3-one, potassium sorbate, parahydroxy benzoates and the like.
  • Pigments may also be included in the formulation and may include but are not limited to pigment blue 15:4, pigment blue 15:3, pigment blue 15:2, pigment blue 15:1 , pigment blue 80, pigment yellow 1 , pigment yellow 13, pigment red 112, pigment red 48:2, pigment red 48:1 , pigment red 57: 1 , pigment red 53:1 , pigment orange 43, pigment orange 34, pigment orange 5, pigment green 36, pigment green 7, pigment white 6, pigment brown 25, basic violet 10, basic violet 49, violet 23, acid red 51 , acid red 52, acid red 14, acid blue 9, acid yellow 23, basic red 10, basic red 108.
  • Polymers such as such polyvinyl alcohols, polyvinylpyrrolidone, gel-forming carraagheenans, water-soluble gelatine and casein, superabsorbent polymers such polyacrylamides and polyacrylates based polymers, Semi-synthetic or fully- synthetic peptide/protein-based superabsorbent polymers such as collagen-based synthetic polymers, elastin-like polypeptides, polyaspartic acid, polyaspartates, polyglutamic acid, polyglutamate, Semi-synthetic or fully-synthetic polysaccharide: carboxymethyl starch , sulfoethyl starch, carboxymethyl cellulose, sulfoethyl cellulos, hydroxypropyl cellulose, hydroxyethyl cellulose, methylcellulose, chitosan; cross-linked polysaccharides such as CMS cross-linked with multi- functional carboxylic acids or multi-functional epoxides and the like.
  • Polysaccharide graft copolymer Polysaccharides obtained by graft polymerizing a monomer onto a polysaccharide, wherein the monomer is selected from acrylonitrile, acrylic acid, methacrylic acid, acrylamide, methacrylamide, 2- acrylamido-2-methyl- propanesulfonic acid (AMPS), vinyl sulfonic acid, ethyl acrylate, and potassium acrylate and the like.
  • AMPS 2- acrylamido-2-methyl- propanesulfonic acid
  • the combination of the present invention are effective against phytopathogenic fungi, especially occurring in plants, including seed borne fungi and belong to the following classes such as those selected from Ascomycetes (e.g. Penicillium, Gaeumannomyces graminis); Basidiomycetes (e.g. the genus Hemileia,
  • Rhizoctonia, Puccinia Rhizoctonia, Puccinia
  • Fungi imperfecti e. g. Botrytis, Helminthosporium, Rhynchosporium, Fusarium, Septoria, Cercospora, Alternaria, Pyricularia and Pseudocercosporella herpotrichoides
  • Oomycetes e. g. Phytophthora, Peronospora, Bremia, Pythium, Plasmopara
  • Zygomycetes e.g., Rhizopus spp.
  • the combination of the present invention is especially effective against Alternaria spp., Ascochyta spp., Aspergillus spp., Claviceps purpurea, Cochliobolus spp., Colletotrichum spp., Diplodia maydis, Erysiphe graminis, Fusarium spp.
  • the present combinations may be used to control insect pests such as those from the order Lepidoptera, for example, Acleris spp., Adoxophyes spp., Aegeria spp., Agrotis spp., Alabama argillaceae, Amylois spp., Anticarsia gemmatalis, Archips spp., Argyrotaenia spp., Autographa spp., Busseola fusca, Cadra cautella, Carposina nipponensis, Chilo spp., Choristoneura spp., Clysia ambiguella, Cnaphalocrocis spp., Cnephasia spp., Cochylis spp., Coleophora spp., Crocidolomia spp., Cryptophlebia leucotreta, Crysodeixis includens, Cydia spp., Diatraea spp.
  • Trogoderma spp. from the order Orthoptera, for example, Blatta spp., Blattella spp., Gryllotalpa spp., Leucophaea maderae, Locusta spp., Periplaneta spp. and Schistocerca spp.; from the order Isoptera, for example, Reticulitermes spp.; from the order Psocoptera, for example, ijposcelis spp.; from the order Anoplura, for example, Haematopinus spp., Linognathus spp., Pediculus spp., Pemphigus spp.
  • Thrips palmi Thrips tabaci and Scirtothrips aurantii; from the order Heteroptera, for example, Dichelops melacanthus, Distantiella theobroma, Dysdercus spp., Euchistus spp., Eurygaster spp., Leptocorisa spp., Nezara spp., Piesma spp., Rhodnius spp., Sahlbergella singularis, Scotinophara spp. and Triatoma spp.
  • Heteroptera for example, Dichelops melacanthus, Distantiella theobroma, Dysdercus spp., Euchistus spp., Eurygaster spp., Leptocorisa spp., Nezara spp., Piesma spp., Rhodnius spp., Sahlbergella singularis, Scotinophara spp. and Triatoma
  • Homoptera for example, Aleurothrixus floccosus, Aleyrodes brassicae, Aonidiella spp., Aphididae, Aphis spp., Aspidiotus spp., Bemisia tabaci, Ceroplaster spp., Chrysomphalus aonidium, Chrysomphalus dictyospermi, Coccus hesperidum, Empoasca spp., Eriosoma larigerum, Erythroneura spp., Gascardia spp., Laodelphax spp.,
  • Lecanium corni Lepidosaphes spp., Macrosiphus spp., Myzus spp., Nephotettix spp., Nilaparvata spp., Paratoria spp., Pemphigus spp., Planococcus spp., Pseudaulacaspis spp., Pseudococcus spp., Psylla spp., Pulvinaria aethiopica, Quadraspidiotus spp., Rhopalosiphum spp., Saissetia spp., Scaphoideus spp., Schizaphis spp., Sitobion spp., Trialeurodes vaporariorum, Trioza erytreae and Unaspis citri; from the order Hymenoptera, for example, Acromyrmex, Athalia rosae, Atta spp.,
  • Vespa spp. from the order Diptera, for example, Antherigona soccata, Bibio hortulanus, , Ceratitis spp., Chrysomyia spp., Culex spp., Cuterebra spp., Dacus spp., Delia spp., Drosophila melanogaster, , Liriomyza spp.
  • Dermanyssus gallinae Eotetranychus carpini, Eriophyes spp., Hyalomma spp., Olygonychus pratensis, Ornithodoros spp., Panonychus spp., Phyllocoptruta oleivora, Polyphagotarsonemus latus, Psoroptes spp., Rhipicephalus spp., Rhizoglyphus spp., Sarcoptes spp., Tarsonemus spp. and Tetranychus spp.; and from the class Nematoda, for example, the species of Meloidogyne spp.
  • Heterodera spp. for example, Heterodera glycines, Heterodera schachtii, Heterodora avenae and Heterodora trifolii
  • Globodera spp. for example, Globodera rostochiensis
  • Radopholus spp. for example, Radopholus similes
  • Rotylenchulus spp. Pratylenchus spp.
  • the combination of the present invention may be used for treatment of plant propagation material of crops such as cereals such as wheat, barley, rye, oats, corn, rice, sorghum, triticale and related crops; beets such as sugar beet and fodder beet; leguminous plants such as beans, lentils, peas, soybean; oil plants such as rape, mustard, sunflowers; cucurbits such as marrows, cucumbers, melons; fibre plants such as cotton, flax, hemp, jute; vegetables such spinach, lettuce, asparagus, cabbages, carrots, onions, tomatoes, potatoes, paprika as well as ornamentals such as flowers, shrubs, broad-leaved trees and evergreens, such as conifers.
  • crops such as cereals such as wheat, barley, rye, oats, corn, rice, sorghum, triticale and related crops
  • beets such as sugar beet and fodder beet
  • leguminous plants such
  • the plant propagation material may also be used on varieties of plant propagation material such as conventional, hybrid or transgenic plants.
  • the combinations of the present invention may further contain herbicide, fungicides, insecticides, fertilizers, biologicals, other plant growth additives such as mycorrhiza, silicic acid, plant derived growth promoters etc.
  • the present invention may provide methods of improving vigour or yield of the plant comprising, applying to a plant propagation material before sowing, a combination comprising:
  • a benzimidazole fungicide selected from carbendazim or thiophanate methyl
  • an active agent selected from imidacloprid, acetamiprid, thiamethoxam, or a multi-site fungicide or both.
  • the multi-site fungicide is a dithiocarbamate fungicide.
  • the dithiocarbamate fungicide is mancozeb.
  • the multi-site fungicide is a phthalimide fungicide selected from captan, captafol and folpet.
  • the multi-site fungicide is a chloronitrile fungicide such as chlorothalonil.
  • the multi-site fungicide is a sulfamide fungicide selected from dichlofluanid and tolylfluanid. In an embodiment, the multi-site fungicide is a bis-guanidine fungicide selected from guazatine and iminoctadine.
  • the multi-site fungicide is a triazine fungicide selected from anilazine.
  • the multi-site fungicide is a quinone fungicide selected from dithianon. In an embodiment, the multi-site fungicide is a quinoxaline fungicide selected from quinomethionate and chlorquinox. In an embodiment, the multi-site fungicide is a dicarboxamide fungicide selected from fluoroimide.
  • the multi-site fungicide is an inorganic fungicide selected from copper fungicides including copper (II) hydroxide, copper oxychloride, copper (II) sulfate, basic copper sulfate, Bordeaux mixture, copper salicylate C7H 4 03*Cu, cuprous oxide CU2O; or sulphur.
  • copper fungicides including copper (II) hydroxide, copper oxychloride, copper (II) sulfate, basic copper sulfate, Bordeaux mixture, copper salicylate C7H 4 03*Cu, cuprous oxide CU2O; or sulphur.
  • the present invention may provide methods of controlling soil borne fungi and insect pests, the method comprising, applying to a plant propagation material before sowing, a combination comprising:
  • a benzimidazole fungicide selected from carbendazim or thiophanate methyl
  • an active selected from imidacloprid, acetamiprid, thiamethoxam, mancozeb, maneb, zineb, folpet, chlorothalonil, and tribasic copper sulfate or a multi-site fungicide or both.
  • the multi-site fungicide is a dithiocarbamate fungicide.
  • the dithiocarbamate fungicide is mancozeb.
  • the multi-site fungicide is a phthalimide fungicide selected from captan, captafol and folpet.
  • the multi-site fungicide is a chloronitrile fungicide such as chlorothalonil.
  • the multi-site fungicide is a sulfamide fungicide selected from dichlofluanid and tolylfluanid.
  • the multi-site fungicide is a bis-guanidine fungicide selected from guazatine and iminoctadine.
  • the multi-site fungicide is a triazine fungicide selected from anilazine.
  • the multi-site fungicide is a quinone fungicide selected from dithianon.
  • the multi-site fungicide is a quinoxaline fungicide selected from quinomethionate and chlorquinox.
  • the multi-site fungicide is a dicarboxamide fungicide selected from fluoroimide.
  • the multi-site fungicide is an inorganic fungicide selected from copper fungicides including copper (II) hydroxide, copper oxychloride, copper (II) sulfate, basic copper sulfate, Bordeaux mixture, copper salicylate C7H 4 03*Cu, cuprous oxide CU2O; or sulphur.
  • the combination of the present invention may be presented as a kit of parts, or as a ready mix formulation that may be readily applied to the plant propagation material or may be applied to plant propagation material before being commercially vended.
  • the combination of the invention could be adapted to a violet color associated to the "optical brightness” providing nighttime brightness through black light, making it difficult to falsify the product and aiding the differentiation of grain for treated seed.
  • the combinations displayed improvement of the plant defense mechanism against pathogens. It promoted the growth of the seedlings through the increment of the root system, with greater depth of roots and better utilization of nutrients. Increased photosynthetic, consequently lower energy consumption of the seedling providing vigorous growth, conditioning the plant to achieve superior productivity even under stress conditions
  • the combinations of the invention facilitated better coverage of seeds due to adherence products through a differentiated and specific formulation for the treatment of seeds, consequently less loss of active ingredient.
  • Example 2 The combination UPL2 according to the present invention was tested for seed treatment advantages in dry bean, and compared vis-a-vis the industry standard of thiadicarb 225 g/L and imidacloprid 75 g/L.
  • the dry bean seeds were treated with the following regimen, and the percentage control of Bemisia tabaci nymphs was calculated using Abbott’s formula. The following results were tabulated:

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Abstract

Disclosed herein is a seed treatment combination of fipronil; azoxystrobin; at least one benzimidazole fungicide; and either a multi-site fungicide or a neonicotinoid insecticide.

Description

NOVEL AGROCHEMICAL COMBINATIONS
Field of the invention:
The present invention relates to agrochemical combinations for the control of plant pests. More particularly, the present invention relates to novel combinations, compositions comprising these combinations and methods of using the combinations for the treatment of plant propagation material.
Background and Prior art:
Combination of insecticides and fungicides are used to broaden the spectrum of control of insect and fungal pests, reduce dosage, thereby reducing environmental impact, and decrease chances of development of resistance. The combination of insecticides and fungicides at times demonstrate an additive or synergistic effect that results in an improved control on the pests.
Damage to seeds from insect and fungal pests is another major concern for agriculturalist. There are various diseases such as seed rot etc. which reduce germination rates and cause considerable decrease in yield. Treating the seed with insecticidal and fungicidal combinations helps reduce damage from such soil pests. Another advantage of treating seeds or other plant propagation material is the improvement in germination rates, increased yield and improved plant health.
There are many combinations of insecticide and fungicide known in the art for the control of soil borne pests. For example, US5877194A teaches combinations of fipronil and triticonazole for seed treatment. US7732374B2 teaches combinations of prothioconazole and insecticides for the control of pests in seeds, soils etc.
There is however a need for improvement of these combinations. Single active combinations used over a long period of time has resulted in resistance. With the onset of resistance to certain pests, there is a need in the art for a combination of actives that decreases chances of resistance and improves the spectrum of disease and pest control. Objects of the invention:
Therefore, one object of the present invention is to provide improved combinations of insecticides and fungicides for the control of soil borne pests. Another object of the present invention is to provide a method and a composition for controlling insect pests and fungal diseases around plant propagation material.
Yet another object of the present invention is to provide improved combinations of insecticides and fungicides that promote plant health.
Embodiment of the present invention can ameliorate one or more of the above mentioned problems.
Summary of the Invention:
Therefore an aspect of the present invention can provide combinations of fipronil; azoxystrobin; at least one benzimidazole fungicide; and either a multi-site fungicide or a neonicotinoid insecticide.
Another aspect of the present invention can provide a method of improving yield in crops, the method comprising applying, to a plant propagation material of said crop, a combination comprising fipronil, azoxystrobin, at least one benzimidazole fungicide and either a multi-site fungicide or a neonicotinoid insecticide.
Yet another aspect of the present invention can provide a method of improving plant health, the method comprising applying, to a plant propagation material of said crop, a combination comprising fipronil, azoxystrobin, a benzimidazole fungicide and either a multi-site fungicide or a neonicotinoid insecticide.
Another aspect of the present invention can provide a composition for treating plant propagation material, the composition comprising fipronil, azoxystrobin, at least one benzimidazole fungicide and either a multi-site fungicide or a neonicotinoid insecticide. In another aspect, the present invention can provide a method of controlling pests by treating a plant propagation material with a composition comprising fipronil, azoxystrobin, at least one benzimidazole fungicide and either a multi-site fungicide or a neonicotinoid insecticide.
In yet another aspect, the present invention can provide a composition for improving plant health, the method comprising applying to a plant propagation material of said crop, a combination comprising fipronil, azoxystrobin, a benzimidazole fungicide and either a multi-site fungicide or a neonicotinoid insecticide.
Detailed Description of the Invention:
The term "plant propagation material" refers to the parts of the plant, such as seeds, which can be used for the propagation of the plant and vegetative plant material such as cuttings and tubers (for example, potatoes). There may be mentioned, e.g., the seeds (in the strict sense), roots, fruits, tubers, bulbs, rhizomes, parts of plants. Germinated plants or young plants, which may be transplanted after germination or after emergence from the soil. "Insecticidal" refers to the ability of a substance to increase mortality or inhibit, growth rate of insects. “Fungicidal” refers to the ability of a substance to decrease or inhibit growth of fungi. The term“agriculturally acceptable amount of active” refers to an amount of an active that kills or inhibits the plant disease for which control is desired, in an amount not significantly toxic to the plant being treated. To“control” or“controlling” insects means to inhibit, through a toxic effect, the ability of insect pests to survive, grow, feed, and/or reproduce, or to limit insect-related damage or loss in crop plants or denotes control and prevention of a disease. Controlling effects include all deviation from natural development, for example: killing, retardation, decrease of the fugal disease or insect pest. To“control” insects may or may not mean killing the insects, although it preferably means killing the insects. The term“agriculturally acceptable amount of active” refers to an amount of an active that kills or inhibits the plant disease for which control is desired, in an amount not significantly toxic to the plant being treated.
The term“improved seed vigour” refers to seed properties that determines potential for fast and uniform emergence, and development of seedlings under a wide range of field conditions, when compared with the same trait in a control plant which has been grown under the same conditions in the absence of the method of the invention. Such traits may include, early and/or improved germination, improved emergence, increased root growth, a developed root system, increased root nodulation, increased shoot growth, improvement in plant height, an increase in plant weight (fresh or dry), bigger leaf blades, greener leaf colour, increased pigment content, increased photosynthetic activity, earlier flowering, longer panicles, early grain maturity, increased seed, fruit or pod size, increased pod or ear number, increased seed number per pod or ear, increased seed mass, enhanced seed filling, delay of senescence, and improved vitality of the plant.
The present inventors found unexpected synergy when fipronil and azoxystrobin was combined with a benzimidazole fungicide and either a multi-site fungicide or a neonicotinoid insecticide. More specifically, the present inventors found unexpected synergy when fipronil and azoxystrobin was combined with either carbendazim or thiophanate methyl and either imidacloprid or a multi-site fungicide or both.
Fipronil is a phenylpyrazole insecticide which acts on the insects’ central nervous system by blocking GABA-gated chloride channels and glutamate-gated chloride channels. Its chemical name is (RS)-5-amino-1-[2,6-dichloro-4- (trifluoromethyl)phenyl]-4- (trifluoromethylsulfinyl)-1 H-pyrazole-3-carbonitrile.
Azoxystrobin is a systemic fungicide belonging to the strobilurin class of compounds. Its mode of action is bought about by attaching to the Qo site of Complex III of the mitochondrial electron transport chain, thereby preventing production of ATP. Its chemical name is methyl (E)-2-{2-[6-(2- cyanophenoxy)pyrimidin-4-yloxy]phenyl}-3-methoxyacrylate.
Benzimidazole fungicides inhibit mitosis and cell division in fungi. They are broad spectrum fungicides that are known to control a wide variety of fungi.
Neonicotinoid insecticides are systemic with contact and stomach action. Acetylcholine receptor (nAChR) agonist. These insecticides are known to control a broad spectrum of insect pests.
Multi-site fungicides are known to attack fungi at multiple sites. These fungicides are used for broad-spectrum disease control. Known multi-site fungicides include but are not limited to dithiocarbamates, phthalimides, chloronitriles, inorganic fungicides, sulfamides, bis-guanidines, triazines, quinones, quinoxalines, dicoarboxamides etc.
The present inventors believe that the combination of the present invention surprisingly results in a synergistic action. The combinations of the present invention allow for a broad spectrum of pest control and has surprisingly improved plant vigour and yield. The broad spectrum of the present combination also provides a solution for preventing the development of resistance.
Therefore, an aspect of the present invention can provide combinations comprising:
i) fipronil;
ii) azoxystrobin;
iii) a benzimidazole fungicide; and
iv) at least one active agent selected from a neonicotinoid insecticide or a multi-site fungicide or both.
In an embodiment, the benzimidazole fungicide is selected from at least one of albendazole, benomyl, carbendazim, chlorfenazole, cypendazole, debacarb, fuberidazole, mecarbinzid, rabenzazole, thiabendazole, furophanate, thiophanate, thiophanate-methyl.
In an embodiment, the benzimidazole fungicide is selected from benomyl, carbendazim and thiophanate or thiophanate-methyl.
In an embodiment, the benzimidazole fungicide is carbendazim.
In an embodiment, the benzimidazole fungicide is thiophanate methyl.
In an embodiment, the multi-site fungicide is a fungicide selected from the group consisting of dithiocarbamates, phthalimides, chloronitriles, inorganic fungicides, sulfamides, bis-guanidines, triazines, quinones, quinoxalines, and di carboxamides.
In an embodiment, the dithiocarbamate fungicide is selected from asamobam, asomate, azithiram, carbamorph, cufraneb, cuprobam, disulfiram, ferbam, metam, nabam, tecoram, thiram, urbacide, ziram, dazomet, etem, milneb, mancopper, mancozeb, maneb, metiram, polycarbamate, propineb and zineb.
In a preferred embodiment, the dithiocarbamate fungicide is selected from maneb, mancozeb and zineb.
In another embodiment, the dithiocarbamate fungicide is mancozeb.
In an embodiment, the multi-site fungicide is a phthalimide fungicide selected from captan, captafol and folpet.
In an embodiment, the multi-site fungicide is a chloronitrile fungicide such as chlorothalonil. In an embodiment, the multi-site fungicide is a sulfamide fungicide selected from dichlofluanid and tolylfluanid.
In an embodiment, the multi-site fungicide is a bis-guanidine fungicide selected from guazatine and iminoctadine.
In an embodiment, the multi-site fungicide is a triazine fungicide selected from anilazine. In an embodiment, the multi-site fungicide is a quinone fungicide dithianon.
In an embodiment, the multi-site fungicide is a quinoxaline fungicide selected from quinomethionate and chlorquinox. In an embodiment, the multi-site fungicide is a dicarboxamide fungicide selected from fluoroimide.
In an embodiment, the multi-site fungicide is an inorganic fungicide selected from copper fungicides including copper (II) hydroxide, copper oxychloride, copper (II) sulfate, basic copper sulfate, Bordeaux mixture, copper salicylate C7H403*Cu, cuprous oxide CU2O; or sulphur.
In an embodiment, the neonicotinoid insecticide may be selected from the group consisting of acetamiprid, clothianidin, imidacloprid, nitenpyram, nithiazine, thiacloprid and thiamethoxam.
In a preferred embodiment, the neonicotinoid insecticide is selected from the group consisting of acetamiprid, thiamethoxam and imidacloprid. Thus, an embodiment of the present invention can provide combinations for treatment of plant propagation material comprising:
i) fipronil; ii) azoxystrobin;
iii) a benzimidazole fungicide selected from carbendazim or thiophanate- methyl; and
iv) at least one active agent selected from imidacloprid, acetamiprid, thiamethoxam, mancozeb, maneb, zineb, folpet, chlorothalonil, and tribasic copper sulfate.
Another embodiment of the present invention may provide combinations for treatment of plant propagation material comprising:
i) fipronil;
ii) azoxystrobin;
iii) a benzimidazole fungicide selected from carbendazim or thiophanate methyl; and
iv) imidacloprid.
Another embodiment of the present invention may provide combinations comprising:
i) fipronil;
ii) azoxystrobin;
iii) a benzimidazole fungicide selected from carbendazim or thiophanate methyl; and
iv) mancozeb.
Another embodiment of the present invention may provide combinations comprising:
i) fipronil;
ii) azoxystrobin
iii) carbendazim; and
iv) imidacloprid.
Another embodiment of the present invention may provide combinations comprising: i) fipronil;
ii) azoxystrobin;
iii) carbendazim; and
iv) mancozeb.
Another embodiment of the present invention may provide combinations comprising
i) fipronil;
ii) azoxystrobin;
iii) thiophanate methyl; and
iv) mancozeb.
Another embodiment of the present invention may provide combinations comprising:
i) fipronil;
ii) azoxystrobin;
iii) thiophanate methyl; and
iv) imidacloprid.
Another embodiment of the present invention can provide combinations for treatment of plant propagation material comprising:
i) fipronil;
ii) azoxystrobin;
iii) a benzimidazole fungicide selected from carbendazim or thiophanate- methyl; and
iv) acetamiprid.
Another embodiment of the present invention can provide combinations for treatment of plant propagation material comprising:
i) fipronil;
ii) azoxystrobin; iii) a benzimidazole fungicide selected from carbendazim or thiophanate- methyl; and
iv) thiamethoxam.
Yet another embodiment of the present invention can provide combinations for treatment of plant propagation material comprising:
i) fipronil;
ii) azoxystrobin;
iii) a benzimidazole fungicide selected from carbendazim or thiophanate- methyl; and
iv) chlorothalonil.
Yet another embodiment of the present invention can provide combinations for treatment of plant propagation material comprising:
i) fipronil;
ii) azoxystrobin;
iii) a benzimidazole fungicide selected from carbendazim or thiophanate- methyl; and
iv) tribasic copper sulfate.
In an embodiment, the constituent fungicides of the combination of the present invention may be admixed in ratio of (1-80): (1-80): (1-80): (1-80) of the fipronil, azoxystrobin, benzimidazole fungicide, neonicotinoid or multi-site fungicide respectively.
The combinations of the present invention may be admixed with suitable agrochemical adjuvants to form compositions.
Thus, an aspect of the present invention may provide a seed treatment composition comprising:
i) fipronil;
ii) azoxystrobin; iii) a benzimidazole fungicide selected from carbendazim or thiophanate methyl;
iv) an active selected from neonicotinoid or a multi-site fungicide or both; and
v) agrochemcially acceptable adjuvants.
Another aspect of the present invention may provide a seed treatment composition comprising:
i) fipronil;
ii) azoxystrobin;
iii) a benzimidazole fungicide selected from carbendazim or thiophanate methyl;
iv) at least one active agent selected from imidacloprid, acetamiprid, thiamethoxam, mancozeb, maneb, zineb, folpet, chlorothalonil, and tribasic copper sulfate; and
v) agrochemcially acceptable adjuvants.
In an embodiment, the total amount of fipronil in the composition may typically be in the range of 0.1 to 99% by weight, preferably 0.2 to 90% by weight. The total amount of azoxystrobin in the composition may be in the range of 0.1 to 99% by weight. The total amount of benzimdazole inhibitor in the composition may be in the range of 0.1 to 99% by weight. The total amount of neonicotinoid in the composition may be in the range of 0.1 to 99% by weight or the total amount of multi-site fungicide in the composition may be in the range of 0.1 to 99% by weight.
In an embodiment, the constituent fungicides and insecticides of the composition of the present invention may be admixed in ratio of (1-80): (1-80): (1-80): (1-80) of the fipronil, azoxystrobin, benzimidazole fungicide and either neonicotinoid or multi-site fungicide respectively. In an embodiment, the constituents of the composition of the present invention may be applied as per known methods of application to seeds and other plant propagation material or transplanted saplings. In an embodiment of the present invention, the compositions can be formulated into either solid or liquid formulations that are suitable for application to plant propagation material. The formulation may be made as known formulation types such as wettable powders (WP), solutions (LS), emulsions (ES), suspension concentrates (FS), water dispersible granule (WG), or aqueous suspension concentrate (CS).
The formulation may be applied by various methods such methods using conventional treating techniques and machines, such as fluidized bed techniques, the roller mill method, rotostatic seed treaters, and drum coaters, spouted beds etc. Pre and post coating procedures such as sizing etc., may also be carried out. Such procedures are known in the art. It is readily understood that plant propagation material will be treated only once it is removed from the plant and is ready to be re-sown. In an embodiment, the treatment may occur before sowing of the plant propagation material so that the sown material has been pre-treated with the combination. In particular, seed coating or seed pelleting are preferred in the treatment of the combinations according to the invention. As a result of the treatment, the active ingredients in the combination are adhered on to the seed and therefore available for pest and/or disease control.
The formulations may contain standard agriculturally acceptable adjuvants, carriers, diluents, emulsifiers, fillers, anti-foaming agents, thickening agents, anti freezing agents, biocides, pigments etc.
Suitable agricultural adjuvants and carriers may include, but are not limited to, crop oil concentrates; methylated seed oils, emulsified methylated seed oil, nonylphenol ethoxylate; benzylcocoalkyldimethyl quaternary ammonium salt; blend of petroleum hydrocarbon, alkyl esters, organic acid, and anionic surfactant; C9-C11 alkylpolyglycoside; phosphated alcohol ethoxylate; natural primary alcohol (C12- C16) ethoxylate; di-sec-butylphenol EO-PO block copolymer; polysiloxane-methyl cap; nonylphenol ethoxylate, urea ammonium nitrate; tridecyl alcohol (synthetic) ethoxylate (8EO); tallow amine ethoxylate ; PEG(400) dioleate-99, alkyl sulfates, such as diethanolammonium lauryl sulfate; alkylarylsulfonate salts, such as calcium dodecylbenzenesulfonate; alkylphenol-alkylene oxide addition products, such as nonylphenol-Cis ethoxylate; alcohol-alkylene oxide addition products, such as tridecyl alcohol-Ci6 ethoxylate; soaps, such as sodium stearate; alkyl- naphthalene-sulfonate salts, such as sodium dibutylnaphthalenesulfonate; dialkyl esters of sulfosuccinate salts, such as sodium di(2-ethylhexyl)sulfosuccinate; sorbitol esters, such as sorbitol oleate; quaternary amines, such as lauryl trimethylammonium chloride; polyethylene glycol esters of fatty acids, such as polyethylene glycol stearate; block copolymers of ethylene oxide and propylene oxide; salts of mono and dialkyl phosphate esters; vegetable or seed oils such as soybean oil, rapeseed/canola oil, olive oil, castor oil, sunflower seed oil, coconut oil, corn oil, cottonseed oil, linseed oil, palm oil, peanut oil, safflower oil, sesame oil, tung oil and the like; and esters of the above vegetable oils, and in certain embodiments, methyl esters.
Suitable liquid carriers that may be employed in a composition of the present invention may include water or organic solvents. The organic solvents include, but are not limited to, petroleum fractions or hydrocarbons such as mineral oil, aromatic solvents, paraffinic oils, and the like; vegetable oils such as soybean oil, rapeseed oil, olive oil, castor oil, sunflower seed oil, coconut oil, corn oil, cottonseed oil, linseed oil, palm oil, peanut oil, safflower oil, sesame oil, tung oil and the like; esters of the above vegetable oils; esters of monoalcohols or dihydric, trihydric, or other lower polyalcohols (4-6 hydroxy containing), such as 2-ethyl hexyl stearate, n-butyl oleate, isopropyl myristate, propylene glycol dioleate, di-octyl succinate, di-butyl adipate, di-octyl phthalate and the like; esters of mono, di and polycarboxylic acids and the like. Organic solvents include, but are not limited to toluene, xylene, petroleum naphtha, crop oil, acetone, methyl ethyl ketone, cyclohexanone, trichloroethylene, perchloroethylene, ethyl acetate, amyl acetate, butyl acetate, propylene glycol monomethyl ether and diethylene glycol monomethyl ether, methyl alcohol, ethyl alcohol, isopropyl alcohol, amyl alcohol, ethylene glycol, propylene glycol, glycerine, N-methyl-2-pyrrolidinone, N,N-dimethyl alkylamides, dimethyl sulfoxide.
Solid carriers that may be employed in the compositions of the present invention may include but are not limited to attapulgite, pyrophyllite clay, silica, kaolin clay, kieselguhr, chalk, diatomaceous earth, lime, calcium carbonate, bentonite clay, Fuller's earth, talc, cottonseed hulls, wheat flour, soybean flour, pumice, wood flour, walnut shell flour, lignin, cellulose etc.
Thickeners such as silicates such meal silicates, sodium carboxymethyl cellulose, methyl cellulose, ethyl cellulose, polyvinylalcohol, sodium alginate, Sodium poly acrylate, xanthan gum, welan gum, gum arabic, montmorillonite, lignosulfonates, hydroxy methyl cellulose, dextrin, starch and mixtures thereof;
Anti-freezing agents such as glycerin, ethylene glycol, propylene glycol, preferably propylene glycol and the like. Anti-foaming agents such as silicone oils, mineral oils, Fatty acid ester; biocides such as sodium benzoate, 1 ,2-benzisothiazoline - 3-one, 2-methyl-4-isothiazolin-3-one, 5-chloro-2-methyl-4-isothiazolin-3-one, potassium sorbate, parahydroxy benzoates and the like. Pigments may also be included in the formulation and may include but are not limited to pigment blue 15:4, pigment blue 15:3, pigment blue 15:2, pigment blue 15:1 , pigment blue 80, pigment yellow 1 , pigment yellow 13, pigment red 112, pigment red 48:2, pigment red 48:1 , pigment red 57: 1 , pigment red 53:1 , pigment orange 43, pigment orange 34, pigment orange 5, pigment green 36, pigment green 7, pigment white 6, pigment brown 25, basic violet 10, basic violet 49, violet 23, acid red 51 , acid red 52, acid red 14, acid blue 9, acid yellow 23, basic red 10, basic red 108. Polymers such as such polyvinyl alcohols, polyvinylpyrrolidone, gel-forming carraagheenans, water-soluble gelatine and casein, superabsorbent polymers such polyacrylamides and polyacrylates based polymers, Semi-synthetic or fully- synthetic peptide/protein-based superabsorbent polymers such as collagen-based synthetic polymers, elastin-like polypeptides, polyaspartic acid, polyaspartates, polyglutamic acid, polyglutamate, Semi-synthetic or fully-synthetic polysaccharide: carboxymethyl starch , sulfoethyl starch, carboxymethyl cellulose, sulfoethyl cellulos, hydroxypropyl cellulose, hydroxyethyl cellulose, methylcellulose, chitosan; cross-linked polysaccharides such as CMS cross-linked with multi- functional carboxylic acids or multi-functional epoxides and the like.
Polysaccharide graft copolymer: Polysaccharides obtained by graft polymerizing a monomer onto a polysaccharide, wherein the monomer is selected from acrylonitrile, acrylic acid, methacrylic acid, acrylamide, methacrylamide, 2- acrylamido-2-methyl- propanesulfonic acid (AMPS), vinyl sulfonic acid, ethyl acrylate, and potassium acrylate and the like.
The combination of the present invention are effective against phytopathogenic fungi, especially occurring in plants, including seed borne fungi and belong to the following classes such as those selected from Ascomycetes (e.g. Penicillium, Gaeumannomyces graminis); Basidiomycetes (e.g. the genus Hemileia,
Rhizoctonia, Puccinia); Fungi imperfecti (e. g. Botrytis, Helminthosporium, Rhynchosporium, Fusarium, Septoria, Cercospora, Alternaria, Pyricularia and Pseudocercosporella herpotrichoides); Oomycetes (e. g. Phytophthora, Peronospora, Bremia, Pythium, Plasmopara); Zygomycetes (e.g., Rhizopus spp.). The combination of the present invention is especially effective against Alternaria spp., Ascochyta spp., Aspergillus spp., Claviceps purpurea, Cochliobolus spp., Colletotrichum spp., Diplodia maydis, Erysiphe graminis, Fusarium spp. (such as Fusarium culmorum, Fusarium oxysporum, Fusarium solani, Fusarium graminearum and Fusarium moniliforme, Fusarium subglutinans), Gaeumannomyces graminis, Giberella fujikuroi, Giberella zeae, Helminthosporium spp. (such as Helminthosporium graminearum, Helminthosporium oryzae, Helminthosporium solani), Monographella nivalis, Penicillium spp., Puccinia spp., Pyrenophora spp. (such as Pyrenophora graminea), Peronosclerospora spp., Peronspora spp., Phakopsora pachyrhizi, Phythium spp., Phoma spp., Phomopsis spp., Rhizoctonia spp. (such as Rhizoctonia cerealis, Rhizoctonia solani), Septoria spp., Pseudocercosporella spp., Tilletia spp., Rhizopus spp., Thielaviopsis basicola, Typhula spp., Ustilago spp., Sphacelotheca spp. (e.g. Spacelotheca reilliani), Thanatephorus cucumeris, and Verticillium spp.
The present combinations may be used to control insect pests such as those from the order Lepidoptera, for example, Acleris spp., Adoxophyes spp., Aegeria spp., Agrotis spp., Alabama argillaceae, Amylois spp., Anticarsia gemmatalis, Archips spp., Argyrotaenia spp., Autographa spp., Busseola fusca, Cadra cautella, Carposina nipponensis, Chilo spp., Choristoneura spp., Clysia ambiguella, Cnaphalocrocis spp., Cnephasia spp., Cochylis spp., Coleophora spp., Crocidolomia spp., Cryptophlebia leucotreta, Crysodeixis includens, Cydia spp., Diatraea spp., Diparopsis castanea, Earias spp., Elasmopalpus spp., Ephestia spp., Eucosma spp., Eupoecilia ambiguella, Euproctis spp., Euxoa spp., Grapholita spp., Hedya nubiferana, Heliothis spp., Hellula undalis, Hyphantria cunea, Keiferia lycopersicella, Leucoptera scitella, Lithocollethis spp., Lobesia botrana, Lymantria spp., Lyonetia spp., Malacosoma spp., Mamestra brassicae, Manduca sexta, Operophtera spp., Ostrinia nubilalis, Pammene spp., Pandemis spp., Panolis flammea, Pectinophora gossypiella, Phthorimaea operculella, Pieris rapae, Pieris spp., Plutella xylostella, Prays spp., Scirpophaga spp., Sesamia spp., Sparganothis spp., Spodoptera spp., Synanthedon spp., Thaumetopoea spp., Tortrix spp., Trichoplusia ni and Yponomeuta spp.; from the order Coleoptera, for example, Agriotes spp., Anthonomus spp., Atomaria linearis, Ceutorhynchus spp., Chaetocnema tibialis, Cosmopolites spp., Curculio spp., Dermestes spp., Diabrotica spp., Epilachna spp., Eremnus spp., Gonocephalum spp., Heteronychus spp., Leptinotarsa decemlineata, Lissorhoptrus spp., Melolontha spp., Orycaephilus spp., Otiorhynchus spp., Phlyctinus spp., Phyllotreta spp., Popillia spp., Protostrophus spp., Psylliodes spp., Rhizopertha spp., Scarabeidae, Sitophilus spp., Sitotroga spp., Tenebrio spp., Tribolium spp. and Trogoderma spp.; from the order Orthoptera, for example, Blatta spp., Blattella spp., Gryllotalpa spp., Leucophaea maderae, Locusta spp., Periplaneta spp. and Schistocerca spp.; from the order Isoptera, for example, Reticulitermes spp.; from the order Psocoptera, for example, ijposcelis spp.; from the order Anoplura, for example, Haematopinus spp., Linognathus spp., Pediculus spp., Pemphigus spp. and Phylloxera spp.; from the order Mallophaga, for example, Damalinea spp. and Trichodectes spp.; from the order Thysanoptera, for example, Frankliniella spp., Hercinothrips spp., Taeniothrips spp. , Thrips palmi, Thrips tabaci and Scirtothrips aurantii; from the order Heteroptera, for example, Dichelops melacanthus, Distantiella theobroma, Dysdercus spp., Euchistus spp., Eurygaster spp., Leptocorisa spp., Nezara spp., Piesma spp., Rhodnius spp., Sahlbergella singularis, Scotinophara spp. and Triatoma spp. ; from the order Homoptera, for example, Aleurothrixus floccosus, Aleyrodes brassicae, Aonidiella spp., Aphididae, Aphis spp., Aspidiotus spp., Bemisia tabaci, Ceroplaster spp., Chrysomphalus aonidium, Chrysomphalus dictyospermi, Coccus hesperidum, Empoasca spp., Eriosoma larigerum, Erythroneura spp., Gascardia spp., Laodelphax spp.,
Lecanium corni, Lepidosaphes spp., Macrosiphus spp., Myzus spp., Nephotettix spp., Nilaparvata spp., Paratoria spp., Pemphigus spp., Planococcus spp., Pseudaulacaspis spp., Pseudococcus spp., Psylla spp., Pulvinaria aethiopica, Quadraspidiotus spp., Rhopalosiphum spp., Saissetia spp., Scaphoideus spp., Schizaphis spp., Sitobion spp., Trialeurodes vaporariorum, Trioza erytreae and Unaspis citri; from the order Hymenoptera, for example, Acromyrmex, Athalia rosae, Atta spp., Cephus spp., Diprion spp., Diprionidae, Gilpinia polytoma, Hoplocampa spp., Lasius spp., Monomorium pharaonis, Neodiprion spp., Solenopsis spp. and Vespa spp.; from the order Diptera, for example, Antherigona soccata, Bibio hortulanus, , Ceratitis spp., Chrysomyia spp., Culex spp., Cuterebra spp., Dacus spp., Delia spp., Drosophila melanogaster, , Liriomyza spp. , , Melanagromyza spp., , Orseolia spp., Oscinella frit, Pegomyia hyoscyami, Phorbia spp., Rhagoletis pomonella, Sciara spp.,; from the order Acarina, for example, Acarus siro, Aceria sheldoni, Aculus schlechtendali, Amblyomma spp., Argas spp., , Brevipalpus spp., Bryobia praetiosa, Calipitrimerus spp., Chorioptes spp.,
Dermanyssus gallinae, Eotetranychus carpini, Eriophyes spp., Hyalomma spp., Olygonychus pratensis, Ornithodoros spp., Panonychus spp., Phyllocoptruta oleivora, Polyphagotarsonemus latus, Psoroptes spp., Rhipicephalus spp., Rhizoglyphus spp., Sarcoptes spp., Tarsonemus spp. and Tetranychus spp.; and from the class Nematoda, for example, the species of Meloidogyne spp. (for example, Meloidogyne incoginita and Meloidogyne javanica), Heterodera spp. (for example, Heterodera glycines, Heterodera schachtii, Heterodora avenae and Heterodora trifolii), Globodera spp. (for example, Globodera rostochiensis), Radopholus spp. (for example, Radopholus similes), Rotylenchulus spp., Pratylenchus spp. (for example, Pratylenchus neglectans and Pratylenchus penetrans), Aphelenchoides spp., Helicotylenchus spp., Hoplolaimus spp., Paratrichodorus spp., Longidorus spp., Nacobbus spp., Subanguina spp. Belonlaimus spp., Criconemella spp., Criconemoides spp. Ditylenchus spp., Dolichodorus spp., Hemicriconemoides spp., Hemicycliophora spp., Hirschmaniella spp., Hypsoperine spp., Macroposthonia spp., Melinius spp., Punctodera spp., Quinisulcius spp., Scutellonema spp., Xiphinema spp., and Tylenchorhynchus spp.
In an embodiment, the combination of the present invention may be used for treatment of plant propagation material of crops such as cereals such as wheat, barley, rye, oats, corn, rice, sorghum, triticale and related crops; beets such as sugar beet and fodder beet; leguminous plants such as beans, lentils, peas, soybean; oil plants such as rape, mustard, sunflowers; cucurbits such as marrows, cucumbers, melons; fibre plants such as cotton, flax, hemp, jute; vegetables such spinach, lettuce, asparagus, cabbages, carrots, onions, tomatoes, potatoes, paprika as well as ornamentals such as flowers, shrubs, broad-leaved trees and evergreens, such as conifers. The plant propagation material may also be used on varieties of plant propagation material such as conventional, hybrid or transgenic plants. In an embodiment, the combinations of the present invention may further contain herbicide, fungicides, insecticides, fertilizers, biologicals, other plant growth additives such as mycorrhiza, silicic acid, plant derived growth promoters etc. In an aspect, the present invention may provide methods of improving vigour or yield of the plant comprising, applying to a plant propagation material before sowing, a combination comprising:
i) fipronil;
ii) azoxystrobin;
iii) a benzimidazole fungicide selected from carbendazim or thiophanate methyl; and
iv) an active agent selected from imidacloprid, acetamiprid, thiamethoxam, or a multi-site fungicide or both.
In an embodiment, the multi-site fungicide is a dithiocarbamate fungicide.
In an embodiment, the dithiocarbamate fungicide is mancozeb.
In an embodiment, the multi-site fungicide is a phthalimide fungicide selected from captan, captafol and folpet.
In an embodiment, the multi-site fungicide is a chloronitrile fungicide such as chlorothalonil.
In an embodiment, the multi-site fungicide is a sulfamide fungicide selected from dichlofluanid and tolylfluanid. In an embodiment, the multi-site fungicide is a bis-guanidine fungicide selected from guazatine and iminoctadine.
In an embodiment, the multi-site fungicide is a triazine fungicide selected from anilazine.
In an embodiment, the multi-site fungicide is a quinone fungicide selected from dithianon. In an embodiment, the multi-site fungicide is a quinoxaline fungicide selected from quinomethionate and chlorquinox. In an embodiment, the multi-site fungicide is a dicarboxamide fungicide selected from fluoroimide.
In an embodiment, the multi-site fungicide is an inorganic fungicide selected from copper fungicides including copper (II) hydroxide, copper oxychloride, copper (II) sulfate, basic copper sulfate, Bordeaux mixture, copper salicylate C7H403*Cu, cuprous oxide CU2O; or sulphur.
In another aspect, the present invention may provide methods of controlling soil borne fungi and insect pests, the method comprising, applying to a plant propagation material before sowing, a combination comprising:
i) fipronil;
ii) azoxystrobin;
iii) a benzimidazole fungicide selected from carbendazim or thiophanate methyl; and
iv) an active selected from imidacloprid, acetamiprid, thiamethoxam, mancozeb, maneb, zineb, folpet, chlorothalonil, and tribasic copper sulfate or a multi-site fungicide or both.
In an embodiment, the multi-site fungicide is a dithiocarbamate fungicide.
In an embodiment, the dithiocarbamate fungicide is mancozeb.
In an embodiment, the multi-site fungicide is a phthalimide fungicide selected from captan, captafol and folpet.
In an embodiment, the multi-site fungicide is a chloronitrile fungicide such as chlorothalonil. In an embodiment, the multi-site fungicide is a sulfamide fungicide selected from dichlofluanid and tolylfluanid. In an embodiment, the multi-site fungicide is a bis-guanidine fungicide selected from guazatine and iminoctadine.
In an embodiment, the multi-site fungicide is a triazine fungicide selected from anilazine.
In an embodiment, the multi-site fungicide is a quinone fungicide selected from dithianon.
In an embodiment, the multi-site fungicide is a quinoxaline fungicide selected from quinomethionate and chlorquinox.
In an embodiment, the multi-site fungicide is a dicarboxamide fungicide selected from fluoroimide. In an embodiment, the multi-site fungicide is an inorganic fungicide selected from copper fungicides including copper (II) hydroxide, copper oxychloride, copper (II) sulfate, basic copper sulfate, Bordeaux mixture, copper salicylate C7H403*Cu, cuprous oxide CU2O; or sulphur. In an aspect, the combination of the present invention may be presented as a kit of parts, or as a ready mix formulation that may be readily applied to the plant propagation material or may be applied to plant propagation material before being commercially vended. Surprisingly, it has been found by the present inventors that combinations of fipronil, azoxystrobin, a benzimidazole fungicide and at least one of Imidacloprid or a multi-site fungicide when applied individually, was ineffective in the control of soil borne fungi and insect pests, but demonstrated excellent synergistic control on weeds when applied together. The combination controlled the soil borne fungi and insect pests. The combination of fipronil, azoxystrobin, a benzimidazole fungicide and at least one of Imidacloprid or a multi-site fungicide controlled seed borne diseases such as seed rot among others. The current invention therefore provides advantageous methods of soil borne fungal and insect pests. The present method also provides a broader spectrum of controlling such pests and helps in resistance management, thus improving germination rate and producing plants with improved vigour and a broader spectrum of control at lower use rates.
Advantages of the present invention:
The combinations of the present invention exert at least one of the following advantages:
These combinations prevent mycelial development, spore germination and the formation of apressories and hautoria, controlling the main soil and seed pathogens such as Rhizoctonia solani and Sclerotinia sclerotiorum. The combinations were found to be totally selective for the cultures and not interfering in the organisms responsible for nodulation in legumes, containing the first multisite fungicide for seed treatment that has multiple action in relation to the cellular functions of the pathogens, forms a barrier on the surface of the seeds. The combinations of the invention thus eliminated the fungi present on the surface of the seeds and prevented germination of the spores that come after the treatment, presenting synergistic effect among the three fungicides, potentiated by mancozeb. The storage time of the thus treated seeds was found to be greater than 120 days without interfering with the germination and vigor patterns.
The combination of the invention could be adapted to a violet color associated to the "optical brightness" providing nighttime brightness through black light, making it difficult to falsify the product and aiding the differentiation of grain for treated seed. The combinations displayed improvement of the plant defense mechanism against pathogens. It promoted the growth of the seedlings through the increment of the root system, with greater depth of roots and better utilization of nutrients. Increased photosynthetic, consequently lower energy consumption of the seedling providing vigorous growth, conditioning the plant to achieve superior productivity even under stress conditions
The combinations of the invention facilitated better coverage of seeds due to adherence products through a differentiated and specific formulation for the treatment of seeds, consequently less loss of active ingredient.
Example:
Experiments were carried out to study the combinations of the present invention for seed treatment in corn. These studies were aimed at verifying the efficacy of doses of the combinations of the inventions, when compared to the standard products. The following combinations were tank-mixed and used for treating corn seeds.
Figure imgf000024_0001
Figure imgf000025_0001
These combinations were used to treat corn seeds before sowing, and the treated seeds were tested for plant strength after emergence. The plant strength was tested by measuring the percentage of plants found laid (fallen) at 70 days after emergence in the field. The following results were tabulated:
Table 1 :
Figure imgf000025_0002
It was thus concluded that the plants emerging from the seeds treated with the combinations according to the present invention displayed surprisingly improved plant strength.
Example 2: The combination UPL2 according to the present invention was tested for seed treatment advantages in dry bean, and compared vis-a-vis the industry standard of thiadicarb 225 g/L and imidacloprid 75 g/L. The dry bean seeds were treated with the following regimen, and the percentage control of Bemisia tabaci nymphs was calculated using Abbott’s formula. The following results were tabulated:
Table 2:
Figure imgf000026_0001
The percentage control (%) for adults + nymphs of Bemisia tabaci was also calculated using Abbott’s formula and tabulated as below: Table 3:
Figure imgf000027_0001
It was thus concluded that the combinations of the present invention were surprisingly efficacious for the control of Bemisia tabaci nymphs and adults during the treatment of dry bean seeds.
While the foregoing written description of the invention enables one of ordinary skill to make and use what is considered presently to be the best mode thereof, those of ordinary skill will understand and appreciate the existence of variations, combinations, and equivalents of the specific embodiment, method, and examples herein. The invention should therefore not be limited by the above described embodiment, method, and examples, but by all embodiments and methods within the scope and spirit of the invention.

Claims

1. A seed treatment combination comprising:
a. fipronil;
b. azoxystrobin;
c. a benzimidazole fungicide; and
d. at least one active agent selected from a neonicotinoid insecticide or a multi-site fungicide or both.
2. The combination as claimed in claim 1 wherein benzimidazole fungicide is selected from albendazole, benomyl, carbendazim, chlorfenazole, cypendazole, debacarb, fuberidazole, mecarbinzid, rabenzazole, thiabendazole, furophanate, thiophanate, thiophanate-methyl.
3. The combination as claimed in claim 1 wherein multi-site fungicide is a fungicide selected from the group consisting of dithiocarbamates, phthalimides, chloronitriles, inorganic fungicides, sulfamides, bis- guanidines, triazines, quinones, quinoxalines, and dicarboxamides.
4. The combination as claimed in claim 1 wherein the dithiocarbamate fungicide is selected from asamobam, asomate, azithiram, carbamorph, cufraneb, cuprobam, disulfiram, ferbam, metam, nabam, tecoram, thiram, urbacide, ziram, dazomet, etem, milneb, mancopper, mancozeb, maneb, metiram, polycarbamate, propineb and zineb;
phthalimide fungicide is selected from captan, captafol and folpet;
chloronitrile fungicide is chlorothalonil;
sulfamide fungicide is selected from dichlofluanid and tolylfluanid;
bis-guanidine fungicide is selected from guazatine and iminoctadine;
multi-site fungicide is a triazine fungicide selected from anilazine;
the multi-site fungicide is a quinone fungicide dithianon;
the multi-site fungicide is a quinoxaline fungicide selected from quinomethionate and chlorquinox is a dicarboxamide fungicide selected from fluoroimide;
inorganic fungicide selected from copper fungicides including copper (II) hydroxide, copper oxychloride, copper (II) sulfate, basic copper sulfate, Bordeaux mixture, copper salicylate C7H403*Cu, cuprous oxide CU20; or sulphur.
5. The combination as claimed in claim 1 wherein neonicotinoid insecticide may be selected from the group consisting of acetamiprid, clothianidin, imidacloprid, nitenpyram, nithiazine, thiacloprid and thiamethoxam.
6. A combination as claimed in claim 1 wherein the said combination comprises:
a. Fipronil, azoxystrobin, carbendazim; and mancozeb
b. Fipronil, azoxystrobin, carbendazim; and Imidacloprid
c. Fipronil, azoxystrobin, thiophanate methyl; and mancozeb d. Fipronil, azoxystrobin, thiophanate methyl; and Imidacloprid e. Fipronil, azoxystrobin, carbendazim; and acetamiprid
f. Fipronil, azoxystrobin, thiophanate methyl; and acetamiprid g. Fipronil, azoxystrobin, carbendazim; and thiamethoxam
h. Fipronil, azoxystrobin, thiophanate methyl; and thiamethoxam i. Fipronil, azoxystrobin, carbendazim; and chlorothalonil
j. Fipronil, azoxystrobin, thiophanate methyl; and chlorothalonil k. Fipronil, azoxystrobin, carbendazim; and tribasic copper sulfate
L. Fipronil, azoxystrobin, thiophanate methyl; and tribasic copper sulfate
7. A combination as claimed in claim 1 wherein the said combination is admixed in the ratio of (1-80): (1-80): (1-80): (1-80).
8. A composition comprising a combination as claimed in claims 1 - 7.
9. A composition as claimed in claim 8, wherein fipronil is present in the range of 0.1 to 99% by weight; azoxystrobin is present in the range of 0.1 to 99% by weight; benzimdazole inhibitor is present in the range of 0.1 to 99% by weight; neonicotinoid is present in the range of 0.1 to 99% by weight or multi site fungicide is present in the range of 0.1 to 99% by weight.
10. A method of improving vigour or yield of the plant comprising, applying to a plant propagation material before sowing, a combination as claimed in claim 1-8
11. A method of controlling soil borne fungi and insect pests, the method comprising, applying to a plant propagation material before sowing, a combination comprising a combination as claimed in claim 1-8
12. A kit comprising a kit of parts, or as a ready mix formulation that may be readily applied to the plant propagation material or may be applied to plant propagation material seed treatment combination as claimed in claims 1-8
PCT/IB2018/060686 2018-01-17 2018-12-28 Novel agrochemical combinations Ceased WO2019142044A1 (en)

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PE2020000937A PE20200934A1 (en) 2018-01-17 2018-12-28 AGROCHEMICAL COMBINATION CONTAINING FIPRONIL, AZOXYSTROBIN, (CARBENDAZIM, THIOPHANTATE OR METHYL THIOPHANTATE) AND (ACETAMIPRID, IMIDACLOPRID, MANCOZEB OR BASIC COPPER SULFATE)
MX2020007450A MX2020007450A (en) 2018-01-17 2018-12-28 Novel agrochemical combinations.
CU2020000049A CU24634B1 (en) 2018-01-17 2018-12-28 FUNGICIDE COMBINATION FOR SEED TREATMENT

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