AGRICULTURAL MIXTURES COMPRISING CARBOXAMIDE COMPOUNDS

Abstract

The present invention relates to agricultural mixtures comprising, as an active ingredient, a carboxamide pesticide and at least one fungicidal active ingredient selected from azoles, strobilurins, carboxamides, carbamates, heterocyclics, and other compounds defined in the description, in synergistically effective amounts. The invention also relates to methods and the use of these mixtures for controlling insects, arachnids, nematodes, and fungi harmful to plants, and for protecting plants against pest infestation, in particular, also for protecting seeds.

Description

AGRICULTURAL MIXTURES COMPRISING COMPOUNDS OF CARBOXAMIDE The present invention relates to mixtures of active ingredients having a synergistically enhanced action and to methods comprising the application of such mixtures. A typical problem that arises in the field of pest and / or fungal control is the need to reduce the dosage rates of the active ingredient in order to reduce or avoid adverse environmental or toxicological effects and, at the same time, allow effective pest and / or fungal control. Another problem is the need for available active pesticide agents that are effective against a broad spectrum of pests. Another problem is the need for available fungicidal active agents that are effective against a broad spectrum of fungi. Another essential problem of the present invention is the desire to obtain compositions that improve plants, a process that is generally known as phytosanitary and will be referred to as such from now on.For example, advantageous properties that can be mentioned are improved crop characteristics, including: emergence, crop yield, protein content, a more developed root system, increased shoots, greater plant height, larger leaf blades, fewer dead basal leaves, stronger shoots, greener leaf color, pigment content, photosynthetic activity, less need for fertilizer, less need for seeds, more productive shoots, earlier flowering, earlier grain maturation, less plant vers (leaning), greater shoot growth, better plant vigor, greater upright plant posture, and better and earlier germination; or any other advantage known to a person of average skill. In general, methods are needed to improve plant health by applying active compounds to the plants or the site. Another object of the present invention, which aims to reduce application rates and broaden the spectrum of activity of active compounds I and II, is to provide mixtures that, by applying a smaller total amount of active compounds, have better activity against animal pests and harmful fungi. Therefore, an object of the present invention is to provide pesticide mixtures that solve the aforementioned problems. In many regions, combating harmful phytopathogenic fungi is not the only problem farmers face. Harmful insects can also cause significant damage to crops and other plants. An effective combination of fungicidal and insecticidal activity is desired to overcome this problem. Therefore, another object of the present invention is to provide a mixture that has both good fungicidal and insecticidal activity, resulting in a broader spectrum of pesticidal action. It is also necessary to have pest or fungal control agents that combine knockdown activity with prolonged control, that is, fast action with long-term action. Another difficulty related to the use of pesticides or fungicides is that the repeated and exclusive application of a single pesticide compound often leads to the rapid selection of pests that develop natural or adaptive resistance to that active ingredient. Therefore, it is necessary to have pest or fungal control agents that help prevent or overcome resistance. Therefore, an object of the present invention is to provide agricultural mixtures that solve at least one of the analyzed problems, such as reducing the dose administration rate, improving the spectrum of activity, combining inactivating activity with prolonged control, or controlling resistance. It was discovered that this objective is achieved, totally or partially, by combining the active compounds defined below. The present invention relates to agricultural mixtures comprising, as active compounds, bQRynn / i ζπζ / β / υιλι 1) at least one carboxamide compound active as a pesticide I of Formula (I): hQA7nn / l 7Π7 / E / YILI or tautomers, enantiomers, diastereomers or salts thereof, 2) at least one fungicidal active compound II selected from group F consisting of Fl) Respiratory inhibitors Fl 1) Complex III inhibitors at the Qo site (e.g., strobilins): azoxystrobin, coumethoxystrobin, coumoxystrobin, dimoxystrobin, enestroburin, phenaminostrobin, phenoxystrobin / fluphenoxystrobin, fluoxastrobin, kresoxim-methyl, mandestrobin, methaminostrobin, orisastrobin, picoxystrobin, pyraclostrobin, pyramethostrobin, pyroxystrobin, 2-(2-(3-(2,6-dichlorophenyl)-1-methyl-allylidenaminooxymethyl)phenyl)-2-methoxyimino-N-methylacetamide, piribencarb, triclopyricarb / chlorodincarb, famoxadone, fenamidone; Fl 2) Inhibidores del complejo III en el sitio Q¡: ciazofamida, amisulbrom, 2-metilpropanoato de [(3S,6S,7R,8R)-8-bencil-3-[(3acetoxi-4-metox¡-p¡r¡d¡n-2-carbon¡l)am¡no]-6-met¡l-4,9-d¡oxo-1,5dioxonan-7-ilo], 2-metilpropanoato de [(3S,6S,7R,8R)-8-bencil-3[[3-(acetox¡metoxi)-4-metox¡-p¡r¡d¡n-2-carbon¡l]am¡no]-6-met¡l-4,9 dioxo-1,5-dioxonan-7-ilo], 2-methylpropanoate of [(3S,6S,7R,8R)8-bencyl-3-[(3-isobutoxol-carbonylox-4-methoxy-p-r-d-n2-carbonyl)amino]-6-methyl-4,9-d-oxo-1,5-dioxonan-7-yl], 2-methylpropanoate of [(3S,6S,7R,8R)-8-bencyl-3-[[3-(1,3benzod-oxol-5-ylmethoxy-)-4-methoxy-pyridin-2-carbonyl]amino]-6methyl-4,9-dioxo-1,5-dioxonan-7-yl]; 2-methylpropanoate de [(3S,6S,7R,8R)-8-bencyl-3-[[3-(1,3-benzodioxol-5-ylmethox)-4methoxy-p¡r¡d¡n-2-carbon¡l]amino]-6-methyl-4,9-dioxo-1,5-dioxonan-7-yl]; 2-methylpropanoate de (3S,6S,7R,8R)-3-[[(3-hydroxy-4methoxy-2-pyridinyl)carbonyl]amino]-6-methyl-4,9-dioxo-8-(phenylmethyl)1,5-dioxonan-7-yl; Fl 3) Complex II inhibitors (e.g., carboxamides): benodanil, benzovindiflupyr, bixaphene, boscalid, carboxin, fenfuram, fluopyram, flutolanil, fluxapiroxad, furametpir, isofetamide, isopyrazam, mepronil, oxycarboxin, pentiopyrrhamine, sedaphenyl, teclophthalam, typhusamide, N-(4'tr¡fluoromethylthiophen¡l-2-¡l)-3-difluoromethyl-1-methyl-1 H-pyrazole-4carboxamide, N-(2-(1,3,3-trime¡l-butyl)-phen¡l)-1,3-dioromethyl-1 H-pyrazol-4-carboxamide, 3-(d if I uo ro methyl I) -1 -methyl-N-(1,1,3trimet¡l¡ndan-4-yl)p¡razol-4-carboxam¡da, 3-(trifluoromethyl)-1 -methylN- (1,1,3-trimethyl-4-carboxamide, 1,3-dimethyl-N(1,1,3-trimethyl-4-l)p¡razol-4-carboxam¡da, 3-(trifluorometh¡l)1,5-dimethyl-N-(1,1,3-trimethylindan-4-yl)pyrazole-4carboxamide, 1,3,5-trimethyl-N-(1,1,3-trim et i I in-4-i I )pure azo I-4carboxamide,N-(7-fluoro-1,1,3-trimethyl-¡dan-4-¡l)-1,3-dimethyl hQA7nn / l 7Π7 / Β / ΥΙΛΙ pyrazole-4-carboxamide, N-[2-(2,4-dichlorophenyl)-2-methoxy¡-1-methylethyl]-3-(difluoromethyl)-1-methyl-pyrazole-4-carboxamide; N-[2-(2,4difluorophen¡l)phen¡l]-3-(trifluoromet¡l)pyrazín-2-carboxamide;, Fl 4) Other respiratory inhibitors (e.g., complex I, uncouplers): diflumetorim, (5,8-difluoroquinoline-4-11)-{2[2-fluoro-4-(4-trifluoromethylpyridine-2-12oxy)-phenyl]-ethyl}-amine; nitrophenyl derivatives: binapacryl, dinobuton, dinocap, fluazinam; ferimzone; organometal compounds: fentin salts, such as fentin acetate, fentin chloride, or fentin hydroxide; ametoctradin; and siltiofam; F.ll) Sterol biosynthesis inhibitors (SBI fungicides) F.ll 1) Inhibidores de C14 desmetilasa (fungicidas DMI): triazoles: azaconazol, bitertanol, bromuconazol, ciproconazol, difenoconazol, diniconazol, diniconazol-M, epoxiconazol, fenbuconazol, fluquinconazol, flusilazol, flutriafol, hexaconazol, imibenconazol, ipconazol, metconazol, miclobutanil, oxpoconazol, paclobutrazol, penconazol, propiconazol, protioconazol, simeconazol, tebuconazol, tetraconazol, triadimefon, triadimenol, triticonazol,uniconazol, - [reí- (2 S ;3 R)-3-(2-el o roph en i I) - 2-(2,4-d if I uo roph en i I)-oxiran i I met i I] 5-t¡ ocian ato-1 H-[1,2,4]triazole,2-[re / -(2S;3R)-3-(2-chlorophenyl)-2(2,4-difluorophenyl)-oxiranylmethyl]-2H-[1,2,4]triazol-3-thiol,2- [2-chloro4-(4-chlorophenoxy)phenyl]-1-(1,2,4-tr¡azol-1-¡l)pentan-2-ol,1-[4-(4chlorophenoxy)-2-(trifluoromethyl)phen¡l]-1 -cyclopropy 1-2-(1,2,4-tri az o I -1 hQA7nn / l 7Π7 / Ε / ΥΙΛΙ il)ethanol,2-[4-(4-chlorophenoxy)-2-(tr¡fluoromethyl)phen¡l]-1 -(1,2,4-tri az o I -1 -yl)butan-2-ol,2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1,2,4t r¡ azo I -1 -yl)butan-2-ol,2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]3-methyl-1 - (1,2,4-triazol-1 -yl)butan-2-ol,2-[4-(4-chlorophenoxy¡)-2(trifluoromethyl)phenyl]-1 - (1,2,4-triazol-1 - yl)propan-2-ol,2-[2-chloro-4(4-chlorophenoxy)phen¡l]-3-methyl-1 -(1,2-1,4-triazol -yl)butan-2-ol,2-[4(4-chlorophenoxy)-2-(trifluoromet¡l)phen¡l]-1 - (1,2,4-tri azo I-1 - i I) pen tan 2-ol,2-[4-(4-fluorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,2-I )propan-2-ol;imidazoles: ¡mazalil, pefurazoate, prochloraz, triflumizole; pyrimidines, pyridines and piperazines: fenarimol, nuarimol, pyrifenox, triporin, [3-(4-chloro-2-fluoro-phenyl)-5-(2,4difluorophenyl)isoxazol-4-yl]-(3-pyridyl)methanol; F.ll 2) Deltal 4-reductase inhibitors: aldimorph, dodemorph, dodemorph-acetate, fenpropimorph, tridemorph, fenpropidin, piperalin, spiroxamine; F.ll 3) 3-keto reductasa inhibitors: fenhexamid; F.111) Nucleic acid synthesis inhibitors F.lll 1) Acylamino acid or phenylamide fungicides: benalaxyl, benalaxyl-M, kiralaxyl, metalaxyl, metalaxyl-M (mefenoxam), ofurace, oxadixyl; F.lll 2) Others: himexazole, octylinone, oxolinic acid, bupyrimate, 5-fluorocytosine, 5-fluoro-2-(p-tolylmethoxy)pyrim¡din-4amine, 5-fluoro-2-(4-fluorophenylmethoxy)p¡r¡m¡din-4-am¡na; F.IV) Inhibitors of cell division and cytoskeleton F.IV 1) Tubulin inhibitors, such as benzimidazoles, hQAJnn / l 7P7 / B / YILI thiophanates: benomyl, carbendazim, fuberidazole, thiabendazole, thiophanate-methyl; triazolopyrimidines: 5-chloro7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)[1,2,4]triazolo[1,5-a]pyrimidine; F.IV 2) Other inhibitors of cell division: dietofencarb, etaboxam, pencicuron, f I uop¡ col id a, zoxamide, metrafenone, pyriofenone; FV) Inhibitors of amino acid and protein synthesis FV 1) Inhibitors of methionine synthesis (anilinopyrimidines): cyprodinil, mepanipyrim, pyrimethanil; FV 2) Protein synthesis inhibitors: blasticidin-S, kasugamycin, kasugamycin hydrochloride, mildiomycin, streptomycin, oxytetracycline, polyoxin, validamycin A; F.VI) Signal transduction inhibitors F.VI 1) MAP / histidine kinase inhibitors: fluoroimid, iprodione, procymidone, vinclozolin, fenpiclonil, fludioxonil; F.VI 2) G protein inhibitors: quinoxifen; F.VII) Inhibitors of lipid and membrane synthesis F.VII 1) Inhibitors of phospholipid biosynthesis: edifenfos, iprobenfos, pyrazofos, iso proti o I ano; F.VII 2) Lipid peroxidation: dichloran, quintozene, technazene, tolclofos-methyl, biphenyl, chloroneb, etridiazole; F.VII 3) Biosynthesis of phospholipids and deposition of the cell wall: dimethomorph, flumorph, mandipropamid, pirimomorph, bentiavalicarb, iprovalicarb, valifenalate and (4-fluorophenyl) ester hQRjnn / i znz / E / YiAi of N-(1-(1-(4-cyanophenyl)ethansulfonyl)-but-2-yl)carbamic acid; F.VII 4) Compounds that affect cell membrane permeability and fatty acids: propamocarb, propamocarb hydrochloride; F.VII 5) Fatty acid amide hydrolase inhibitors: oxatiapiprolin; F.VIII) Inhibitors with action at multiple sites F.VIII 1) Inorganic active substances: Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, sulfur; F.VIII 2) Thio- and dithiocarbamates: ferbam, mancozeb, maneb, metam, metiram, propineb, thiram, zineb, ziram; F.VIII 3) Organochlorine compounds (for example: phthalimides, sulfonamides, eloroni tr i I os): anilazine, chlorothalonil, captafol, captan, folpet, diclofluanide, dichlorophene, hexachlorobenzene, pentachlorophenol and their salts, phthalide, tolylfluanide, N-(4-chloro-2-nitrophenyl)-N-ethyl-4-methylbenzenesulfonamide; F.VIII 4) Guanidines and others: guanidine, dodine, free base of dodine, guazatine, guazatine-acetate, iminoctadine, iminoctadinatriacetate, im¡noctadina-tr¡s(albes¡lato), ditianon, 2,6-dimethyl1 H,5H-[1,4]dithiino[2,3-c: 5,6-c']dip irro I -1,3,5,7(2H,6H)-tetraona; F.IX) Inhibitors of the synthesis of the cellular wall F.IX 1) Inhibitors of glucan synthesis: validamycin, polyoxin B; F.IX 2) Inhibidores de la síntesis de melanina: piroquilon, hQAJnn / l 7Π7 / Β / ΥΙΛΙ tricyclazol, carpropamida, diciclomet, fenoxanil; FX) Plant defense inductors FX 1) Acibenzolar-S-methylo, probenazol, isotianil, tiadinil, prohexadiona-calcium; FX 2) Phosphonates: fosetyl, fosetyl-aluminium, phosphoric acid and its sales, 4-cycloprop¡lN-(2,4-d¡methox¡phen¡l)t¡ad¡azol-5-carboxamida; F.XI) Unknown method of action: bronopol, quinomethionate, ciflufenamide, cimoxanil, dazomet, debacarb, diclomezin, difenzoquat, difenzoquat-methylsulfate, diphenylamine, phenpyrazamine, flumetover, flusulfamide, flutianil, metasulfocarb, nitrapyrine, nitrotal-isocarpilol, oxapropyl, pitrapizoline, pitrazoline, tolprocarb, 2-[3,5-bis(difluoromethyl)-1 H-pyrazole-1 ¡l]-1-[4-(4-{5-[2-(prop-2-in-1 -yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3¡l}-1,3-thiazol-2-p-¡n yl]ethanone, 2-[3,5-bis(d¡fluoromethyl)1 H-pyrazol-1 -yl]-1 -[4-(4-{5-[2-fluoro-6-(prop-2-in-1 -ilox¡)phen¡l]-4,5d ihi dro-1,2-oxazo I-3-yl}-I-1,3-I-I-I-I-I) - yl]ethanone, 2-[3,5-bis(difluoromet¡l)-1 H-pyrazole-1 - yl]-1-[4-(4-{5-[2-chloro-6(prop-2-in-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-yl p -2) r¡ din -1 -yl]ethanone, copper-oxine, proquinazide, tebufloquine, teclophthalam, triazoxide, 2-butoxy-6-iodo-3-prop¡lchromen-4-one, N(c¡cloprop¡lmethoxyim¡no-(6-d¡fluoro-methoxy¡-2,3-d¡fluoro-phen¡l)methyl)-2-phen¡lacetam¡da,N'-(4-(4-chloro-3-tr¡fluoromethyl-phenoxy¡)-2,5dimethyl-phen¡l)-N-ethyl-N-meth¡lformam¡dine, N'-(4-(4-fluoro-3tr¡fluorometh¡l-phenoxy¡)-2,5-d¡methyl-phen¡l)-N-et¡lN-meth¡lformam¡na, N,-(2-methyl-5-trifluoromethyl-4-(3-trimethylsilanyl-propoxy)-phenyl)-NhQA7nn / l 7Π7 / Β / ΥΙΛΙ ethyl-N-methylformamidine, N'-(5-trifluoromethyl-2-meth¡l-4-(3tr¡methyls¡lan¡l-propox¡)-phen¡l)-N-et¡lN-meth¡lformam¡na, 6-terbutyl-8-fluoro-2,3-d¡met¡l-quinol-acetic acid, 4-acetic acid 3 - [5-(4-methylene I)-2,3-dimethyl I - i soxazo I iden-3 - i I] pyridine, 3 - [5-(4-c I o ro-phene I) - 2,3-dimethi I - i soxazo I i di n - 3-i I ]-pyrisoxazole (amide acid), N-(6-methoxy-p¡r¡d¡n-3yl)cyclopropanecarboxylic,5-chloro-1-(4,6-dimethoxy-pyrimidin-2-yl)-2m et i I -1 H-benzoim¡dazol,2-(4-chloro-phen¡l)-N-[4-(3,4-dimeth¡ox¡phenyl)-¡soxazol-5-yl]-2-prop-2-¡n¡loxy-acetam¡da,(Z)-3-amino-2cyano-3-phenyl-propyl-2N-[6-[[(Z)-[(1 -methyltetrazol-5¡l)-phenyl-meth¡len]am¡no]ox¡met¡l]-2-p¡r¡d¡l]pentyl carbamate, 2[2-[(7,8-difluoro-2-methyl-3-quinolyl-6propane)-propane]- 2-[2-fluoro-6-[(8-fluoro-2-methyl-3-qu¡n¡l)ox¡]phen-¡l]propane-2-ol,3(5-fluoro-3,3,4,4-tetramethyl-3,4-d¡droisoqu¡nol¡n-1 -yl)quinol¡n,3(4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline-1-yl)quinoline,3(4,4,5-trifluoro-3,3-d¡ metí 1-3,4-dihydroisoqu mol in-1 - il,quinol¡n; F.XII) Biopesticides F.XII 1) Microbial pesticides with fungicidal, bactericidal, antiviral and / or plant defense activity: Ampelomyces quisqualis, Aspergillus flavus, Aureobasidium pullulans, Bacillus amyloliquefaciens, B. mojavensis, B. pumilus, B. simplex, B. solisalsi, B. subtilis, B. subtilis var. amyloliquefaciens, Candida oleophila, C. saitoana, Clavibacter michiganensis (bacterióphagos), Coniothyrium minitans, Cryphonectria parasitica, Cryptococcus albidus, Dilophosphora hQRjníMl 7Π7 / Β / ΥΙΛΙ alopecuri, Fusarium oxysporum, Clonostachys rosea f. catenulate (also called Gliocladium catenulatum), Gliocladium roseum, Lysobacter antibioticus, L. enzymogenes, Metschnikowia fructicola, Microdochium dimerum, Microsphaeropsis ochracea, Muscodor albus, Paenibacillus polymyxa, Pantoea vagans, Phlebiopsis gigantea, Pseudomonas sp., Pseudomonas chloraphis, Pseudozyma flocculosa, Pichia anómala, Pythium oligandrum, Sphaerodes mycoparasitica, Streptomyces griseoviridis, S. lydicus, S.violaceusniger, Talaromyces flavus, Trichoderma asperellum, T. atroviride, T. fertile, T. gamsii, T. harmatum; T. harzianum, mixture of T. harzianum and T. viride; mixture of T. polysporum and T. harzianum; T. stromaticum, T. vírens (also called Gliocladium virens), T. viride, Typhula phacorrhiza, Ulocladium oudemansii, Verticillium dahlia, zucchini yellow mosaic virus (antivirulent strain); F.XII 2) Biochemical pesticides with fungicidal, bactericidal, antiviral and / or plant defense activating activity: chitosan (hydrolyzed), hairpin protein, laminarin, menhaden fish oil, natamycin, plum pox virus coating protein, potassium or sodium bicarbonate, Reynoutria sachlinensis extract, salicylic acid, tea tree oil; in synergistically effective quantities. Furthermore, it was discovered that the simultaneous application, i.e., jointly or separately, of one or more active compounds I and one or more active compounds II, or the successive application (i.e., immediately one after the other to create the in-situ mixture at the desired location, e.g., the plant) of one or more active compounds I and one or more active compounds II allows for better control of pests and / or fungi compared to the control rates that are possible with the individual compounds. Furthermore, the present invention includes mixtures comprising more than one fungicidal active compound II selected from group F. Furthermore, the present invention includes mixtures comprising 2, 3 or 4 bQRynn / i ζπζ / β / υιλι fungicidal active compounds II selected from group F. Furthermore, the present invention includes mixtures comprising as an additional active compound III an insecticidal compound selected from group IVl of pesticides. The following List M of pesticides, grouped and numbered according to the Pesticide Resistance Action Committee (IRAC) Mode of Action Classification, with which the compounds according to the invention may be used and with which potential synergistic effects may be produced, is intended to illustrate possible combinations, but without imposing any limitation: M.1 Acetylcholinesterase (AChE) inhibitors of the class of: M.1A carbamates, for example, aldicarb, alanicarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, etiofencarb, fenobucarb, formetanate, furatiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur, thiodicarb, thiophanox, trimetacarb, XMC, xylylcarb, and triazamate; or of the class of M.1B organophosphates, for example, acetate, azamethiphos, azinphosethyl, azinphosmethyl, cadusaphos, chlorethoxyphos, chlorfenvinphos, chlormephos, chlorpyrifos, chlorpyrifos-methyl, coumaphos, cyanophos, demeton-S-methyl, diazinon, dichlorvos / DDVP, dicrotophos, dimethoate, dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, famfur, fenamiphos, fenitrothion, fenthion, fosthiazate, heptenophos, imiciaphos, isofenphos, isopropyl O-(methoxyaminothiophosphoryl) salicylate, isoxathion, malathion, mecarbam, methamidophos, methidathion, mevinphos, monocrotophos, naled, omethoate, oxidemeton-methyl, parathion, parathion-methyl, phentoate, phorate, fosalone, phosmet, fosfamidon, phoxim, pirimiphos-methyl, profenophos, propetamphos, protiophos, pyraclofos, pyridafenthion, quinalfos, sulfotep, tebupirimphos, temephos, terbufos, tetrachlorvinphos, thiometon, triazophos, trichlorfon and vamidothion; M.2. GABA-regulated chloride channel antagonists, for example: M.2A organochlorine cyclodiene compounds, for example, endosulfan or chlordane; or M.2B fiproles (phenylpyrazoles), for example, etiprol, fipronil, flufiprol, pirafluprol and pyriprol; M.3 Sodium channel modulators of the class of: M.3A pyrethroides, for example, acrinatrin, aletrin, d-cis-trans aletrin, d-trans aletrin, bifenthrin, bioalethrin, bioalethrin S-cylclopentenyl, bioresmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha-cypermethrin, hQRjnn / ι znz / E / YiAi beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin, deltamethrin, empentrin, esfenvalerate, etofenprox, fenpropatrin, fenvalerate, f lucitrinato, flumethrin, tau-fluvalinate, halfenprox, heptafluthrin, imiprotrin, meperfluthrin, methofluthrin, momfluorothrin, permethrin, phenothrin, pralethrin, profluthrin, pyrethrin (pyrethrum), resmethrin, silafluofen, tefluthrin, tetramethylfluthrin, tetramethrin, tralomethrin, and transfluthrin; or M.3B Moduladores del canal de sodio, tales como DDT o metoxiccloro; M.4 Nicotine acetylcholine receptor (nAChR) agonists of the class of: M.4A neonicotinoids, for example, acteamiprid, clothianidin, cycloxaprid, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam; or the compounds M.4 A. 2: (2E-)-1-[(6-chlorop¡r¡din-3-¡l)methyl]-N'-nitro-2pentylidenehydrazinecarboximidamide; either M4.A.3:1-[(6-chloropyrid¡n-3-¡l)methyl]-7-methyl-8-nitro-5-propoxy¡-1,2,3,5,6,7hexahudroimidazo[1,2-a]pyridine; or of the M.4B nicotine class; M.5 Allosteric activators of the spinosine class of the nicotinic acetylcholine receptor, e.g., spinosad or spinetoram; M.6 Chloride channel activators of the avermectin and milbemycin class, for example, abamectin, emamectin benzoate, ivermectin, lepimectin or milbemectin; M.7 Youth hormone mimics, for example, Μ.7Α juvenile hormone analogues, such as hydroprene, kinoprene and methoprene; or others, such as M.7B fenoxicarb or M.7C pyriproxyfen; M.8 miscellaneous non-specific (multi-site) inhibitors, for example, M.8A alkyl halides, such as methyl bromide and other alkyl halides, or M.8B chloropicrin, M.8C sulfuryl fluoride, M.8D borax or M.8E tartar emetic; M.9 Selective blockers of homeopteran feeding, for example, M.9B pymetrozine, or M.9C flonicamid; M.10 Mite growth inhibitors, for example, M.10A clofentezine, hexythiazox, or M.10B etoxazole; M.11 Microbial disruptors of insect midgut membranes, for example bacillus thuringiensis or bacillus sphaericus and the insecticidal proteins they produce, such as bacillus thuringiensis subsp. israelensis, bacillus sphaericus, bacillus thuringiensis subsp. aizawai, bacillus thuringiensis subsp. kurstaki and bacillus thuringiensis subsp. tenebrionis, or the Bt culture proteins: CrylAb, CrylAc, CrylFa, Cry2Ab, mCry3A, Cry3Ab, Cry3Bb and Cry34 / 35Ab1; M.12 Mitochondrial ATP synthase inhibitors, for example, M.12A diafenthiuron, or M.12B organotin acaricides, such as azocyclotine, cyhexatin or fenbutatin oxide, or M.12C propargite, or M.12D tetradifon; hQA7nn / l 7Π7 / Β / YΙΛΙ M.13 Uncouplers of oxidative phosphorylation by altering the proton gradient, for example, chlorfenapyr, DNOC or sulfluramid; M.14 Nicotinic acetylcholine receptor (nAChR) channel blockers, e.g., nereistoxin analogues such as bensultap, cartap hydrochloride, thiocyclam or thiosultap sodium; M.15 Inhibitors of type 0 chitin biosynthesis, such as benzoylureas, for example, bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron or triflumuron; M.16 Inhibitors of chitin biosynthesis type 1, for example, buprofezin; M.17 Molting disruptors, Diptera, for example, cyromazine; M.18 Ecdysone receptor agonists, such as diacylhydrazines, for example, methoxyfenozide, tebufenozide, halofenozide, fufenozide or chromafenozide; M.19 Octopamine receptor agonists, e.g., amitraz; M.20 Inhibitors of electron transport of mitochondrial complex III, for example, M.20A hydramethylnon, or M.20B acequinocyl, or M.20C fluacripyrim; M.21 Inhibitors of electron transport of mitochondrial complex I, for example, M.21A METI insecticides and acaricides, such as fenazaquin, fenpyroximate, pirimidifen, pyridaben, tebufenpyrad or tolfenpyrad, or M.21 B rotenone; M.22 Voltage-gated sodium channel blockers, for example, hQA7nn / l Zηζ / E / YΙΛΙ M.22A indoxacarb or M.22B metaflumizone or M.22B.1: 2-[2-(4-cyanophenyl)1 - [3-(trifluoromethyl)phenyl]ethylidene]-N-[4-(difluoromethoxy)phenyl]hydrazinecarboxamide or M.22B.2: N-(3-chloro-2-methylphenyl)-2-[(4chlorophenyl)[4-[methyl(methylsulfonyl)amino]phenyl]methylene]hydrazinecarboxamide; M.23 Acetyl CoA carboxylase inhibitors, such as tetronic and tetramic acid derivatives, for example, spirodiclofen, spiromesifen or spirotetramat; M.24 Inhibitors of electron transport of mitochondrial complex IV, for example, M.24A phosphine, such as aluminum phosphide, calcium phosphide, zinc phosphide or M.24B cyanide; M.25 Inhibitors of electron transport of mitochondrial complex II, such as beta-ketonitrile derivatives, for example, cyenopyrafen or cyflumethophen; M.28 Diamide class ryanodine receptor modulators, e.g., flubendiamide, chlorantraniliprole (rynaxypyr®), cyantraniliprole (cyazypyr®), or phthalamide compounds M.28.1: (R)-3-chlor-N1-{2-methyl-4-[1,2,2,2-tetraf I uor-1 (trifluoromethyl)ethyl]phenyl}-N2-(1-methyl-2-methylsulfonylethyl)phthalamide and M.28.2: (S)-3-chlor-N1-{2-methyl-4-[1,2,2,2 -tetrafluor-1(trifluormethyl)ethyl]phen¡l}-N2-(1 - methyl-2-methylsulfonylethyl)phthalamide or the compound hQA7nn / l 7Π7 / Β / ΥΙΛΙ M.28.3:3-bromo-N-{2-bromo-4-chloro-6-[(1 -cycloprop¡leth¡l)carbamoyl]phen¡l} -(3-chlorpyridin-2-yl)-1 H-pyrazol-5-carboxamide (proposed ISO name: cyclan iIIproI), or the compound M.28.4:methyl-2-[3,5-d¡bromo-2-({[3-bromo-1 -(3-chlorpyride i n-2-11)-1 Hpyrazol-5-yl]carbonyl}amino)benzoyl]-1,2-dimethylhydrazinecarboxylate; or a selected compound of M.28.5a) to M.28.5I): M.28.5a)N-[4,6-dichloro-2-[(d¡et¡l-lambda-4-sulfan¡l¡den)carbamoyl]-phen¡l]2-(3-chloro-2-pyr¡d¡l)-5-(trifluoromet¡l)pyrazole-3-carboxam¡da; M.28.5b)N-[4-chloro-2-[(diethyl-lambda-4-sulfan¡l¡dene)carbamo¡l]-6-met¡lphenyl]-2-(3-chloro-2-p¡r¡d¡l)-5-(tr¡fluorometh¡l)p¡¡fluoromethrazole-3-carboxylate; M.28.5c)N-[4-chloro-2-[(di-2-propyl-lambda-4-sulfan¡l¡den)carbamo¡l]-6methyl-phen¡l]-2-(3-chloro-2-p¡r¡d¡l)-5-(tr¡fluoromethl)p¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡s; M.28.5d)N-[4,6-dichloro-2-[(d¡-2-prop¡l-lambda-4-sulfan¡liden)carbamo¡l]phenyl]-2-(3-chloro-2-p¡r¡d¡l)-5-(trifluoromethyl)p¡ l-3-carboxylate; M.28.5e)N-[4,6-dichloro-2-[(d¡et¡l-lambda-4-sulfan¡l¡dene)carbamoyl]-phen¡l]2-(3-chloro-2-pyr¡d¡l)-5-(difluoromethyl)p¡razol-3-carboxam¡da; M.28.5f)N-[4,6-dibromo-2-[(d¡-2-prop¡l-lambda-4-sulfan¡lidene)carbamo¡l]phenyl]-2-(3-chloro-2-p¡r¡dyl)-5-(tr¡fluoro methi l)p¡ l-3-carboxylate; M.28.5g)N-[4-chloro-2-[(di-2-propyl-lambda-4-sulfan¡l¡den)carbamoyl]-6cyano-phen¡l]-2-(3-chloro-2-p¡r¡d¡l)-5-(tr¡fluorometh¡l)p¡¡¡razole-carboxylate; M.28.5h)N-[4,6-dibromo-2-[(d¡et¡l-lambda-4-sulfan¡l¡dene)carbamo¡l]-phenyl]2-(3-chloro-2-pyr¡d¡l)-5-(tr¡fluoromet¡l)pyrazole-3-carboxam¡da; M.28.5¡)N-[2-(5-amino-1,3,4-t¡ad¡azol·2-¡l)-4-chloro-6-met¡lphen¡l]-3-bromo1 -(3-chloro-2-pyrid¡n¡l)-1 H-pyrazole-5-carboxamide; M.28.5j)3-chloro-1 - (3-chloro-2-pyrid¡nyl)-N-[2,4-d¡chloro-6-[[(1 -cyano-1 methylethyl)amino]carbon¡l]phen¡l]-1 H-pyrazole-5-carboxamide; hQAznn / i znz / E / YiAi M.28.5k)3-bromo-N-[2,4-d¡chloro-6-(meth¡lcarbamoyl)phenyl]-1 -(3,5-dichloro-2pi rid I)-1 H-pyrazol-5-carboxamida; M.28.5l)N-[4-chloro-2-[[(1,1 -dimethylethyl)amino]carbonyl]-6-methylphenyl]-1 -(3chloro-2-pyridinyl)-3-(fluoromethoxy)-1 H-pyrazol-5-carboxamida; or a selected list M.28.6: N-(2-cyanopropan-2-¡l)-N-(2,4-d¡methylphen¡l)-3-¡odobencen-1,2dicarboxamida; or M.28.7: 3-chloro-N-(2-cyanopropan-2-yl)-N-(2,4-d¡meth¡lphenyl)-bencen-1,2dicarboxamida; M.28.8a) 1 -(3-chloro-2-pyr¡dinyl)-N-[4-c¡ano-2-met¡l-6[(met¡lam¡no)carbon¡l]phen¡l]-3-[[5-(tr¡fluoromethyl)-2H-tetrazol-2-¡l]met¡l]- H-pyrazol-5-carboxamide; or M.28.8b)1 - (3-chloro-2-pyridine)-N-[4-cano-2-methyl-6[(methylamine)carbonyl]phenyl]-3-[[5-(tr¡fluoromethyl)-1 H-tetrazol-1 -ylmethyl]- H-pyrazol-5-carboxamide; M.UN. Insecticidal active compounds with an unknown or uncertain mode of action, for example, afoxolaner, azadirachtin, amidoflumet, benzoximate, bifenazate, bromopropylate, quinomethionate, cryolite, dicofol, flufenerim, flometoquin, fluensulfone, fluopyram, flupyradifurone, fluralaner, methoxadizone, piperonyl butoxide, piflubumide, pyridalyl, pyrifluquinazon, sulfoxaflor, thioxazafen, triflumezopyrim, or the compounds M.UN.3:1-(4-chloro-2,6-dimethylphenyl)-1,2-hydroxy-1,4-dioxa-9-azadispiro[4.2.4.2]-tetradec-11-en-1-one, or the compound M.UN.4:3-(4'-fluoro-2,4-dimethylbiphenyl-3-yl)-4-hydroxy-8-oxa-1 bQRynn / i ζπζ / β / υιλι azasp¡ro[4.5]dec-3-en-2-one, or the compound M.UN.5:1 -[2-fluoro-4-met¡l-5-[(2,2,2-trifluoroethyl)sulfin¡l]phen¡l]-3(trifIuorometiI)-1 H-1,2,4-triazol-5-amine, or active based on bacillus firmus (Votivo, 1-1582); or a compound selected from the group of M.UN.6, wherein the compound is selected from M.UN.6a) to M.UN.6k): M.UN.6a) (E / Z)-N-[1 -[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoroacetamide; M.UN.6b)(E / Z)-N-[1-[(6-chloro-5-fluoro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2trifluoro-acetamide; M.UN.6C) in (E / Z)-2,2,2-trifluoro-N-[1-[(6-fluoro-3-pyridyl)methyl]-2pyr¡d¡lidene]acetam¡da; M.UN.6d) (E / Z)-N-[1-[(6-bromo-3-pyridyl)met¡l]-2-pyrid¡l¡den]-2,2,2trifluoro-acetamide; M.UN.6e) (E / Z)-N-[1 -[1 -(6-chloro-3-pyridyl)ethyl]-2-pyridylidene]-2,2,2-trifluoroacetamide; M.UN.6f) (E / Z)-N-[1 -[(6-chloro-3-pyrid¡l)methyl]-2-p¡r¡d¡l¡den]-2,2-d¡fluoroacetamide; M.UN.6g)(E / Z)-2-chloro-N-[1-[(6-chloro-3-p¡rid¡l)methyl]-2-pyr¡dylidene]-2,2difluoro-acetamide; M.UN.6h) (E / Z)-N-[1-[(2-chloropyrimidin-5-yl)methyl]-2-pyridylidene]-2,2,2trifluoro-acetamide; M. UN.6i)(E / Z)-N-[1 -[(6-chloro-3-pi ridyl) methyl]-2-pyridylidene]-2,2,3,3,3pentaflu oro-pro pan amide.); M.UN.6j)N-[1 - [(6-chloro-3-p¡ ridyl) methyl]-2-pyridylidene]-2,2,2-trifluoroQA7nn / l 7Π7 / Β / ΥΙΛΙ thioacetamide or of the compound M.UN.6k)N-[1 -[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-N'isopropyl-acetamidine or compounds M. UN.8:8-chloro-N-[2-chloro-5-methoxyf enyl) su Ifon i]-6-trif luoromethyl) imidazo[1,2-a]pyrid¡n-2-carboxam¡da; either M.UN.9: 4-[5-(3,5-diciorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-2-methylN-(1-oxothiethane-3-yl)benzam¡da; either M.UN.1 0: 5-[3-[2,6-dichloro-4-(3,3-dichloroal¡loxy)phenoxy¡]propox¡]-1 Hpyrazole; or a compound selected from the group of M.UN.11, wherein the compound is selected from M.UN.11b) to M.UN.11 p): M. UN. 11. b)3-(benzoylm ethyl amino) -N-[2-bromo-4-[1,2,2,3,3,3-hexafluoro1 -(tr¡fluoromethyl)prop¡l]-6-(trifluoromet¡l)phenyl]-2-fluoro-benzamide; M.UN.11.c)3-(benzoylmethylam¡no)-2-fluoro-N-[2-¡odo-4-[1,2,2,2tetrafluoro-1 - (trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]-benzamide; M.UN.11 ,d)N-[3-[[2-iodine-4-[1,2,2,2-tetraf I gold-1 -(trif I uo methi I )et¡ I]-6(trifluoromethane)phen¡l]am¡no]carbon]phen¡l]-N-methl;benzene. M.UN.11 .e)N-[3-[[[2-bromo-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-6(trifluoromethyl)phen¡l]am¡no]carbon¡l]-2-fluorophenyl]-4-fluoro-nzamidate; M.UN.11 ,f)4-fluoro-N-[2-fluoro-3-[[[2-iodo-4-[1,2,2,2-tetrafluoro-1 (trif fluoromethyl) ethyl] -6-(trif fluoromethyl )f in il]am i no]carbo ni I ] f enyl] I -benzamidame; M.UN.11 ,g)3-fluoro-N-[2-fluoro-3-[[[2-iodo-4-[1,2,2,2-tetrafluoro-1 (trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]amino]carbon¡l]phenyl]-N-Ryn / methylbQ ζπζ / β / υιλι benzamide; M.UN.11 .h)2-chloro-N-[3-[[[2-iodo-4-[1,2,2,2-tetrafluoro-1 (trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]amino]carbonyl]phenyl]-3pyridinecarboxamide; M.UN.11 .i)4-cano-N-[2-cyano-5-[[2,6-dibromo-4-[1,2,2,3,3,3-hexafluoro1 -(tr¡fluoromet¡l)propyl]phen¡l]carbamo¡l]phenyl]-2-methyl-benzamide; M.UN.11 .j)4-c¡ano-3-[(4-c¡ano-2-methyl-benzo¡l) ami no]-N-[2,6-d icio ro-4[1,2,2,3,3,3-hexafluoro-1 - (trif luoromethyl) propyl]phenyl] -2-fluoro-benzam ¡da; M.UN.11 .k)N-[5-[[2-chloro-6-cyano-4-[1,2,2,3,3,3-hexafluoro-1 (trif luorometil) propyl]fenil]carbamo i I]-2-cían of en il]-4-cyano-2-metí Ibenzamida; M.UN.11 ,l)N-[5-[[2-bromo-6-chloro-4-[2,2,2-trifluoro-1 -hidroxi-1 (trif luoromethyl) ethi I ]f en il]carbamoyl]-2-cyano-phen i I ]-4-ci an ο-2-methylbenzamida; M.UN.11 .m)N-[5-[[2-bromo-6-chloro-4-[1,2,2,3,3,3-hexafluoro-1 (trif luorometil) propyl]fenil]carbamo i I]-2-cían of en il]-4-ciano-2-metí Ibenzamida; M.UN.11 .n)4-cyano-N-[2-cyano-5-[[2,6-d¡chloro-4-[1,2,2,3,3,3-hexafluoro-1 (triflu gold methi l)propyl]phenyl]carbamo yl]phen i I]-2-methi I-benzamide; M.UN.11 .o)4-cyano-N-[2-cyano-5-[[2,6-dichloro-4-[1,2,2,2-tetrafluoro-1 (trifl u oro methi I) eti I ]f en yl]carbamoyl]phen i I] - 2-m et i I-benzamide; M.UN.11 ,p)N-[5-[[2-bromo-6-chloro-4-[1,2,2,2-tetrafluoro-1 (trif luoromethyl) ethyl l]f en yl]carbamoyl]-2-cyano-f en yl]-4-cyan ο-2-methylbenzamide; or a compound selected from the group of M.UN.12, wherein the hQRynn / i ζπζ / β / υιλι compound is selected from M.UN.12a) to M.UN.12m): M.UN.12.a) 2-(1,3-d¡oxan-2-¡l)-6-[2-(3-pyr¡d¡n¡l)-5-t¡azol¡l]-pyr¡d¡na; M.UN.1 2. b) 2-[6-[2-(5-f I uo ro-3-pyridi ni I)-5-ti azole il]-2-pyridine i I]-pyrimidine; M.UN.1 2.c) 2-[6-[2-(3-p¡r¡d¡n¡l)-5-t¡azol¡l]-2-pyr¡dn¡l]-p¡r¡mdina; M.UN.12.d) N-methylsulfonyl-6-[2-(3-pyridyl)thiazol-5-yl]pyridin-2-carboxamide M.UN.1 2.e) N-methylsulfonyl-6-[2-(3-pyridyl)t¡azol-5-yl]pyridin-2-carboxamide M.UN.12. f) N-ethyl-N-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-3-methylthiopropanamide M.UN.1 2. g) N-meth¡lN-[4-methyl-2-(3-p¡r¡d¡l)t¡azol-5-¡l]-3-meth¡lt¡opropanamide M.UN.1 2. h) N,2-dimeth¡lN-[4-methyl-2-(3-p¡r¡d¡l)t¡azol-5-¡l]-3-methl¡opropanamide M.UN.1 2. i) N-et¡l-2-met¡lN-[4-methyl-2-(3-pyrid¡l)t¡azol-5-¡l]-3-met¡lt¡opropanamide M.UN.12. j) N - [4-cl oro-2 - (3-p¡ rid i I) of azo I-5-i I] - N-et i I-2 - met i I-3 - met i 11 io propanamide M.UN.12. k) N-[4-chloro-2-(3-pyr¡d¡l)thiazol-5-¡l]-N,2-d¡met¡l-3-methlthiopropanamide M.UN.1 2.1) N-[4-chlo ro - 2-(3-pyr ¡di I) of azo I-5-i I] - N - met i I-3 - met i I ti o propanamide M.UN.12. (m) N-[4-chloro-2-(3-pyridyl)thiazol-5-yl]-N-ethyl-3-methylthiopropanamide; or the compound M.UN.13: 2-(4-methoxy i mi nocido hexi 1)-2-(3,3,3tr if I uo ro prop i I su If oni I) aceto nitri I o; or the compounds hQA7nn / l 7Π7 / Β / ΥΙΛΙ M.A. 14a) 1 -[(6-chloro-3-pyridinyl)methyl]-1,2,3,5,6,7-hexahydro-5-methoxy¡-7methyl-8-nitro-i midazo[1,2-a]pyridine; either M.UN.14b) 1 - [(6-chloropyridin-3-yl)methyl]-7-methyl-8-nitro-1,2,3,5,6,7hexahydroimidazo[1,2-a]pyridin-5-ol; or the compound M.UN.15:1 -[(2-chloro-1,3-ti azo I - 5-i I) m et i I ]-3-(3,5-d ¡el or of eni I)-9 - m et i I-4oxo-4H-pyr¡do[1,2-a]p¡r¡m¡din-1 -io-2-olate. MY Biopesticides, which are pesticide compounds of biological origin with insecticidal, acaricidal, molluscidal and / or nematicidal activity, which include MY-1: Microbial pesticides: Bacillus firmus, B. thuringiensis ssp. israelensis, B. t. ssp. galleriae, B. t. ssp. kurstaki, Beauveria bassiana, Burkholderia sp., Chromobacterium subtsugae, Cydia pomonella granulosis virus, Isaria fumosorosea, Lecanicillium longisporum, L. muscarium (formerly Verticillium lecanii), Metarhizium anisopliae, M. anisopliae var. acridum, Paecilomyces fumosoroseus, P. lilacinus, Paenibacillus poppiliae, Pasteuria spp., P. nishizawae, P. reneformis, P. usagae, Pseudomonas fluorescens, Steinernema feltiae, Streptomyces galbus; or active ingredients of bacillus firmus (Votivo, 1-1582), or MY-2 Plaguicidas bioquímicos: L-carvone, citral , acetato de (E,Z)-7,9-dodecadien-1 -ilo, formato de ethylo, decadienoato de (E,Z)-2,4-etiIo (áster de pera), (Ζ,Ζ,Ε)7,11,13-hexadecatrienal, butirato de heptilo, miristato de isopropilo, senecioato de lavadulilo, 2-metil 1-butanol, hQA7nn / l 7Π7 / Β / ΥΙΛΙ metil eugenol, jasmonato de metilo, (E,Z)-2,13octadecadien-1-ol, acetato de (E,Z)-2,13-octadecadien-1 ol, (E,Z)-3,1 3-octadecadien-1-ol, R-1-octen-3-ol, pentatermanona, silicato de potasio, actanoato de sorbitol, acetato de (E,Z,Z)-3,8,11 -tetradecatrienilo, acetato de (Z,E)-9,12-tetradecadien-1-ilo, Ζ-7-tetradecen2-ona, acetato de Z-9-tetradecen-1-ilo, Z-11 -tetradecenal, Z-11-tetradecen-1-ol , extracto de la acacia negra, extracto de semillas y pulpa de pomelo, extracto de Chenopodium ambrosiodae, aceite de menta gatuna, aceite de nim, extracto de quillay, aceite de tagetes o componenti del árbol ginkgo selected from the group that consists of bilobalida, ginkgólida A, ginkgólida B,ginkgolide C, ginkgolide J and ginkgolide M;, Furthermore, the present invention includes mixtures comprising more than one additional insecticidal active compound III selected from group M. Furthermore, the present invention includes mixtures comprising more than 2, 3 or 4 fungicidal active compounds II selected from group F, and one or more additional insecticidal active compounds III selected from group M. Furthermore, the present invention relates to: hQA7nn / l Zηζ / E / YΙΛΙ agricultural compositions comprising a mixture of at least one active compound I and at least one active compound II; optionally an additional active compound III; the use of a mixture of at least one active compound I and at least one active compound II (and optionally an additional active compound III) to combat animal pests; the use of a mixture of at least one active compound I and at least one active compound II (and optionally an additional active compound III) to combat harmful phytopathogenic fungi; a method for combating animal pests, comprising bringing animal pests, their habitat, breeding place, food supply, plant, seed, soil, area, material or environment in which animal pests grow or may grow, or materials, plants, seeds, soils, surfaces or spaces to be protected against attack or infestation by animal pests, into contact with a pesticide-effective amount of a mixture of at least one active compound I and at least one active compound II (and optionally an additional active compound III); a method for protecting crops against attack or infestation by phytopathogenic animal and / or fungal pests, comprising contacting a crop with a mixture of at least one active compound I and at least one active compound II (and optionally an additional active compound III); a method for protecting seeds against soil-dwelling insects, and for protecting the roots and shoots of seedlings against foliar and soil-dwelling insects and / or phytopathogenic harmful fungi, comprising contacting the seeds hQRjnn / i znz / E / YiAi before sowing and / or after pre-germination with a mixture of at least one active compound I with at least one active compound II (and optionally an additional active compound III); and seeds comprising a mixture of at least one active compound I and at least one active compound II; (and optionally an additional active compound III). Compound I Carboxamide derivatives that generally exhibit pesticidal activity have been previously described. WO200573165 and WO2010018714 describe carboxamide compounds, their preparation, and use as pest control agents. WO2007013150, JP2011157294, JP2011-157295, and JP2011-157296 describe mixtures of carboxamides with other active ingredients. The preparation of the compounds of Formula I can also be obtained, in accordance with standard methods of organic chemistry, for example, with the methods or working examples described in WO 2010 / 018857 without this implying a limitation to the routes indicated therein. The prior art does not describe agricultural mixtures comprising the selective carboxamide compound, according to the present invention, in combination with other agricultural active compounds that show unexpected synergistic effects with respect to fungicidal and / or insecticidal activity. hQA7nn / l 7Π7 / Β / YΙΛΙ Compound I of Formula (I) includes its tautomers, racemic mixtures, individual pure enantiomers and diastereomers, and its optically active mixtures. Compounds II The active compounds II mentioned above from groups F1 to F11 are chemically active fungicidal pesticides, described by their common names. Their preparation and activity against pests are known (cf.: http: / / www.alanwood.net / pesticides / ); these pesticides are frequently available commercially. Also known are the fungicidal pesticides described by the IUPAC nomenclature, their preparation and their pesticidal activity (cf. Can. J. Plant Sci. 48(6), 587-94, 1968; EP-A 141 317; EP-A 152 031; EP-A 226 917; EP-A 243 970; EP-A 256 503; EP-A 428 941; EP-A 532 022; EP-A 1 028 125; EP-A 1 035 122; EP-A 1 201 648; EP-A 1 122 244, JP 2002316902; DE 19650197; DE 10021412; DE 102005009458; US 3,296,272; US 3,325,503; WO 98 / 46608; WO 99 / 14187; WO 99 / 24413; WO 99 / 27783; WO 00 / 29404; WO 00 / 46148; WO 00 / 65913; W.O. 01 / 54501; WO 01 / 56358; WO 02 / 22583; WO 02 / 40431; WO 03 / 10149; WO 03 / 1 1853; WO 03 / 14103; WO 03 / 16286; WO 03 / 53145;WO 03 / 61388; WO 03 / 66609; WO 03 / 74491; WO 04 / 49804; WO 04 / 83193; WO 05 / 120234; WO 05 / 123689; WO 05 / 123690; WO 05 / 63721;WO 05 / 87772; WO 05 / 87773; WO 06 / 15866; WO 06 / 87325; WO 06 / 87343; WO 07 / 82098; WO 07 / 90624, WO 1 1 / 028657, WO2012 / 168188, WO 2007 / 006670, WO 1 1 / 77514; WO13 / 047749, WO 10 / 069882, WO hQAJnn / l 7Π7 / Β / ΥΙΛΙ 13 / 047441, WO 03 / 16303, WO 09 / 90181, WO 13 / 007767, WO 13 / 010862, WO 13 / 024009 and WO 13 / 024010). Biopesticides (such as Compound II or Compound III) The biopesticides of group MY or F.XII, their preparation and their pesticidal activity, for example, against harmful fungi or insects, are known (e-Pesticide Manual V 5.2 (ISBN 978 1 901396 85 0) (20082011); http: / / www.epa.gov / opp00001 / biopesticides / , see product lists; http: / / www.omri.org / omri-lists, see lists; BioPesticides Database BPDB http: / / sitem.herts.ac.uk / aeru / bpdb / , see A-Z link). Biopesticides of group II.MY or F.XII. may also have insecticidal, fungicidal, acaricidal, molluscidal, antiviral, bactericidal, pheromone, nematicidal, plant defense activator, plant stress reducer, plant growth regulator, plant growth promoter, growth regulator and / or plant yield enhancer activity. Many of these biopesticides are registered and / or commercially available: aluminum silicate (ScreenTM Duo of Certis LLC, USA), Agrobacterium radiobacter K1026 (eg, NoGall® from Becker Underwood Pty Ltd., Australia), A. radiobacter K84 (Nature 280, 697699, 697699; 1979; e.g., GalITroll® from AG Biochem, Inc., C, USA), Ampelomyces quisqualis M-10 (e.g., AQ 10® from Intrachem Bio GmbH & Co. KG, Germany), Ascophyllum nodosum extract or filtrate (e.g., ORKA GOLD from Becker Underwood, 1979; South Africa; or Goemar® of Goemar Laboratories, hQRjnn / ι znz / E / YiAi France), Aspergillus flavus NRRL 21882 released by hand in Georgia in 1991 by USDA, National Peanut Research Laboratory (for example, in Afla-Guard® from Syngenta, CH), mixtures of Aureobasidium pullulans DSM14940 and DSM 14941 (for example, blastoesporas in BlossomProtect® from bio-ferm GmbH, Germany), Azospirillum brasilense XOH (por ejemplo, AZOS de Microbiol. BiotechnoL 17(2), 280-286, 2007; for example, in BioYield® de Gustafson LLC, TX, EE. UU.), B. amyloliquefaciens IT-45 (CNCM I-3800) (por ejemplo, Rhizocell C de ITHEC, France), B. amyloliquefaciens subsp. plantarum MBI600 (NRRL B-50595, deposited in the Department of Agriculture of the United States (for example, Integral®, Subtilex® NG de Becker Underwood, EE. UU.), B. cereus CNCM 1-1562 (US 6,406,690), B.firmus CNCM 1-1582 (WO 2009 / 126473, WO 2009 / 124707, US 6.406.690; Votivo® de Bayer Crop Science LP, USA), B. pumilus GB34 (ATCC 700f Yi,Shimplostald, L® en TX, USA.) and Bacillus pumilus KFP9F (NRRL B50754) (e.g., in BAC-UP or FUSION-P from Becker Underwood South Africa), B. pumilus QST 2808 (NRRL B--30087), (e.g., Agra. UEE.Quest® Plus. subtiUs GB03 (e.g., Kodiak® or BioYield® de Gustafson, Inc., USA; or Companion® de Growth Products, Ltd., White Plains, NY 10603, USA), B. subtilis GB07 de Gustaf.,Epic® hQRjnnn sell / E / YiAi. QST-713 (NRRL B--21661 in Rhapsody®, Serenade® MAX and Serenade® ASO from AgraQuest Inc., USA), B. subtilis var. amyloliquefaciens FZB24 (e.g., Taegro® from Novozyme Biologicals, Inc., USA), B. subtilis var. amyloliquefaciens D747 (e.g., Double Nickel 55 from Certis LLC, USA), B. thuringiensis ssp. aizawai ABTS-1857 (e.g., in XenTari® from BioFa AG, Münsingen, Germany), B. t. ssp. aizawai SAN 401 I, ABG-6305 and ABG-6346, Bacillus t. ssp. israelensis AM65-52 (e.g., in VectoBac® from Valent BioSciences, IL, USA), Bacillus thuringiensis ssp. kurtaki SB4 (NRRL B-50753; e.g., Beta Pro® from Becker Underwood, South Africa), B. t. ssp. kurtaki ABTS-351 identical to HD-1 (ATCC SD-1275; e.g., in Dipel® DF from Valent BioSciences, IL, USA), B. t. ssp. kurtaki EG 2348 (e.g. in Lepinox® or Rapax® from CBC (Europe) Srl, Italy), B. t. ssp. tenebrionis DSM 2803 (EP 0 585 215 B1 ; identical to NRRL B-15939; Mycogen Corp.), B. t. ssp.tenebrionis NB-125 (DSM 5526; EP 0 585 215 B1; also designated SAN 418 I or ABG-6479; previous Novo-Nordisk production strain), B. t. ssp. tenebrionis NB-176 (or NB-176-1) a gamma-irradiated induced high-performance mutant of strain NB-125 (DSM 5480; EP 585 215 B1; Novodor® from Valent BioSciences, Switzerland), Beauveria bassiana ATCC 74040 (eg, in Naturalis® from CBC (Europe); Srl, Italy), B. bassiana DSM 12256 (US 200020031495; e.g., BioExpert® SC from Live Sytems Technology SA, Colombia), B. bassiana GHA (BotaniGard® 22WGP from Laverlam Int. Corp., USA), B. bassiana PPRI 5339 (ARSEF no. 5339). in the collection of entomopathogenic fungal cultures of the Service of hQRjnn / i znz / E / YiAi. USDA Agricultural Research Service (ARS; NRRL 50757) (e.g., BroadBand® from Becker Underwood, South Africa), B. brongniartii (e.g., in Melocont® from Agrifutur, Agrianello, Italy, for the control of the San Juan beetle; J. Appl. Microbiol. 100(5),1063-72, 2006), Bradyrhizobium sp. (e.g., Vault® from Becker Underwood, USA), B. japonicum (e.g., VAULT® from Becker Underwood, USA), Candida oleophila 1-182 (NRRL Y-18846; e.g., Aspire® from Ecogen Inc., USA, Phytoparasitica 23(3), 231-234, 1995), C. oleophila strain O (NRRL Y-2317; Biological Control 51, 403-408, 2009), Candida saitoana (e.g., Biocure® (in mixture with lysozyme) and BioCoat® from Micro Fio Company, USA (BASF SE) and Arysta), chitosan (e.g., Armour-Zen® from BotriZen Ltd., NZ), Clonostachys rosea f.catenulata, also called Gliocladium catenulatum (e.g., isolated J 1446: Prestop® from Verdera Oy, Finland), Chromobacterium subtsugae PRAA4-1 isolated from soil on an eastern spruce (Tsuga canadensis) in the Catoctin Mountain region of central Maryland (e.g., on GRANDEVO from Marrone Bio Innovations, USA).), Coniothyrium minitans CON / M / 91-08 (e.g., Contaos® WG from Prophyta, Germany), Cryphonectria parasitica (e.g., Endothia parasitica from CNICM, France), Cryptococcus albidus (e.g., YIELD PLUS® from Anchor Bio-Technologies, South Africa), Cryptophlebia leucotreta granulovirus (CrleGV) (e.g., in CRYPTEX from Adermatt Biocontrol, Switzerland), Cydia pomonella granulovirus (CpGV) V03 (DSM GV-0006; e.g., in MADEX Max from Andermatt Biocontrol, Switzerland), CpGV V22 (DSM GV-0014; e.g., hQA7nn / l 7P7 / E / YILI in MADEX Twin from Adermatt Biocontrol, Switzerland), Delftia acidovorans RAY209 (ATCC PTA-4249; WO 2003 / 57861; for example, in BIOBOOST by Brett Young, Winnipeg, Canada), Dilophosphora alopecuri (Lidophia graminis by Becker Underwood, Australia), Ecklonia maxima (seaweed) extract (for example, KELPAK SL by Kelp Products Ltd, South Africa), formononetin (for example, in MYCONATE by Plant Health Care, UK), Fusarium oxysporum (for example, BIOFOX® by SIAPA)Italy, FUSACLEAN® from Natural Plant Protection, France), Glomus intraradices (e.g., MYC 4000 from ITHEC, France), Glomus intraradices RTI-801 (e.g., MYKOS from Xtreme Gardening, USA or RTI Reforestation Technologies International, USA), grapefruit seed and pulp extract (e.g., BC-1000 from Chemie SA, Chile), hairpin (alpha-beta) protein (e.g., MESSENGER or HARP-N-Tek from Plant Health Care, UK; Science 257, 1-132, 1992), Heterorhabditis bacteriophaga (e.g., Nemasys® G from Becker Underwood Ltd., UK), Isaria fumosorosea Apopka-97 (ATCC 20874) (PFR-97™ from Certis LLC, USA), cisjasmona (US 8.221.736), laminarin (for example, in VACCIPLANT from Laboratoires Goemar, St. Malo, France or Stáhler SA, Switzerland), Lecanicillium longisporum KV42 and KV71 (for example, VERTALEC® from Koppert BV, Netherlands), L.muscarium KV01 (formerly Verticiilium lecanii) (e.g. MYCOTAL from Koppert BV, The Netherlands), Lysobacter antibioticus 13-1 (Biological Control 45, 288-296, 2008), L. antibioticus HS124 (Curr. Microbiol. 59(6), 608-615, 2009), L. enzymogenes 3.1T8 (Microbiol. Res. 158, 107-1 15; Biological Control hQAJnn / l 7Π7 / Β / ΥΙΛΙ (2), 145-154, 2004), Metarhizium anisopliae var. M. a. acridum IMI 330189 (isolated from Ornithacris cavroisi in Niger; also NRRL 50758) (e.g., GREEN MU SO LE® from Becker Underwood, South Africa), M. a. var. acridum FI-985 (e.g., GREEN GUARD® SC from Becker Underwood Pty Ltd, Australia), M. anisopliae FI-1045 (e.g., BIOCANE® from Becker Underwood Pty Ltd, Australia), M. anisopliae F52 (DSM 3884, ATCC 90448; e.g., MET52® Novozymes Biologicals BioAg Group, Canada), M.anisopliae ICIPE 69 (e.g., METATHRIPOL from ICIPE, Nairobe, Kenya), Metschnikowia fructicola (NRRL Y-30752; e.g., SHEMER® from Agrogreen, Israel, now distributed by Bayer CropSciences, Germany; US 6,994,849), Microdochium dimerum (e.g., ANTIBOT® from Agrauxine, France), Microsphaeropsis ochracea P130A (ATCC 74412 isolated from apple tree leaves in an abandoned orchard, St-Joseph-du-Lac, Quebec, Canada in 1993; Mycologia 94(2), 297-301, 2002), Muscodor albus QST 20799 originally isolated from the bark of a cinnamon tree in Honduras (e.g., in Muscudor™ or QRD300 development products from AgraQuest, USA), neem oil (e.g. TRILOGY®, TRIACT® 70 EC from Certis LLC, USA), Nomuraea rileyi strains SA86101, GU87401, SR86151, CG128 and VA9101, Paecilomyces fumosoroseus FE 9901 (e.g. NO FLY™ from Natural Industries, Inc., USA), P.lilacinus 251 (e.g., in BioAct® / MeloCon® from Prophyta, Germany; Crop Protection 27, 352-361, 2008; originally isolated from infected nematode eggs in the Philippines), P. lilacinus DSM 15169 (e.g., NEMATA® SC from Live Systems hQB7nn / i znz / E / YiAi. Technology SA, Colombia), P. lilacinus BCP2 (NRRL 50756; e.g., PL GOLD from Becker Underwood BioAg SA Ltd, South Africa), mixture of Paenibacillus alvei NAS6G6 (NRRL B-50755), Pantoea vagans (formerly agglomerans) C9-1 (originally isolated in 1994 from apple stem tissue; BlightBan C9-1® from NuFrams America Inc., USA, for the control of apple blight; J. Bacteriol. 192(24) 6486-6487, 2010), Pasteuria spp. ATCC PTA-9643 (WO 2010 / 085795), Pasteuria spp. ATCC SD-5832 (WO 2012 / 064527), P. nishizawae (WO 2010 / 80169), P. penetraos (US 5.248.500), P. ramose (WO 2010 / 80619), P. thornea (WO 2010 / 80169), P. usgae (WO 2010 / 80169), Penicillium bilaiae (e.g., Jump Start® from Novozymes Biologicals BioAg Group, Canada, originally isolated from soil in southern Alberta; Fertilizer Res. 39, 97-103, 1994), Phlebiopsis gigantea (e.g., RotStop® from Verdera Oy, Finland), Pichia anomala WRL-076 (NRRL Y30842; US 8.206.972), potassium bicarbonate (e.g., Amicarb® from Stáhler SA, Switzerland), potassium silicate (e.g., Sil-MATRIX™ from Certis LLC, USA), Pseudozyma flocculosa PF-A22 UL (e.g., Sporodex® from Plant Products Co. Ltd., Canada), Pseudomonas sp. DSM 13134 (WO 2001 / 40441, for example, in PRORADIX from Sourcon Padena GmbH & Co. KG, Hechinger Str. 262, 72072 Tübingen, Germany), P. chloraphis MA 342 (for example, in CERALL or CEDEMON from BioAgri AB, Uppsala, Sweden), P. fluorescens CL 145A (for example, in ZEQUANOX from Marrone BioInnovations, Davis, CA, USA; J. Invertebr. PathoL 1 13(1):104-14, 2013), Pythium oligandrum DV 74 (ATCC 38472; for example, POLYVERSUM® from Remeslo SSRO, hQA7nn / l 7P7 / B / YILI). Biopreparaty, Czech Republic and GOWAN, USA; US 2013 / 0035230), Reynoutria sachlinensis extract (e.g. REGALIA® SC from Marrone Biolnnovations, Davis, CA, USA), Rhizobium leguminosarum bv. phaseolii (e.g. RHIZO-STICK from Becker Underwood, USA), RI trifolii RP113-7 (e.g. DORMAL from Becker Underwood, USA; Appl. Environ. Microbiol. 44(5), 1096-1 101), RI bv. viciae P1NP3Cst (also referred to as 1435; New Phytol 179(1), 224-235, 2008; e.g., in NODULATOR PL Peat Granule from Becker Underwood, USA; or in NODULATOR XL PL from Becker Underwood, Canada), RI bv. viciae SU303 (e.g., NODULAID Group E from Becker Underwood, Australia), RI bv. viciae WSM1455 (e.g., NODULAID Group F from Becker Underwood, Australia), R.tropici SEMIA 4080 (identical to PRF 81; Soil Biology & Biochemistry 39, 867-876, 2007), Sinorhizobium meliloti MSDJ0848 (INRA, France) also designated strain 2011 or RCR2011 (Mol Gen Genomics (2004) 272:109). 117; e.g., DORMAL ALFALFA from Becker Underwood, USA; NITRAGIN® Gold from Novozymes Biologicals BioAg Group, Canada), Sphaerodes mycoparasitica IDAC 301008-01 (WO 201 1 / 022809), Steinernema carpocapsae (e.g., MILLENIUM® from Becker Underwood Ltd.; RU), S. feltiae (NEMASHIELD® from BioWorks, Inc., USA; NEMASYS® from Becker Underwood Ltd., RU), S. kraussei L137 (NEMASYS® L from Becker Underwood Ltd., RU), Streptomyces griseoviridis K61 (eg, MYCOSTOP® from Verdera Oy, Espoo, Finland; Crop Protection 25, 468-475, 2006), S. lydicus WYEC 108 (e.g., Actinovate® from Natural Industries, Inc., USA, US hQRjnn / ι znz / E / YiAi. 5,403,584), S. violaceusniger YCED-9 (e.g., DT-9® from Natural Industries, Inc., USA, US 5,968,503), Talaromyces flavus V117b (e.g., PROTUS® from Prophyta, Germany), Trichoderma asperellum SKT-1 (e.g., ECO-HOPE® from Kumiai Chemical Industry Co., Ltd., Japan), T. asperellum ICC 012 (e.g., in TENET WP, REMDIER WP, BIOTEN WP from Isagro NC, USA, BIO-TAM from AgraQuest, USA), T. atroviride LC52 (e.g., SENTINEL® from Agrimm Technologies Ltd, NZ), T. atroviride CNCM 1-1237 (e.g., in Esquive WG from Agrauxine SA, France, e.g., against diseases caused by pruning injuries in grapevines and plant root pathogens), T. fertile JM41R (NRRL 50759; e.g., RICHPLUS™ from Becker Underwood Bio Ag SA Ltd, South Africa), T. gamsii ICC 080 (e.g., in TENET WP, REMDIER WP, BIOTEN WP from Isagro NC, USA, BIO-TAM from AgraQuest, USA), T. harzianum T22 (e.g., PLANTSHIELD® from BioWorks Inc., USA), T.harzianum TH 35 (e.g., ROOT PRO® from Mycontrol Ltd., Israel), T. harzianum T-39 (e.g., TRICHODEX® and TRICHODERMA 2000® from Mycontrol Ltd., Israel and Makhteshim Ltd., Israel), T. harzianum and T. viride (e.g., TRICHOPEL from Agrimm Technologies Ltd, NZ), T. harzianum ICC012 and T. viride ICC080 (e.g., REMEDIER® WP from Isagro Ricerca, Italy), T. polysporum and T. harzianum (e.g., BINAB® from BINAB Bio-innovation AB, Sweden), T. stromaticum (e.g., TRICOVAB® from CEPLAC, Brazil), T. virens GL-21 (also called Gliocladium virens) (e.g., SOILGARD® from Certis LLC, USA). U.S.), T. viride (e.g., TRIECO® from Ecosense Labs. hQRjnn / i znz / E / YiAi (India) Pvt. Ltd., Indien, BIO-CURE® F from T. Stanes & Co. Ltd., India), T. viride TV1 (e.g. T. viride TV1 from Agribiotec srl, Italy) and Ulocladium oudemansii HRU3 (e.g. in BOTRY-ZEN® from BotryZen Ltd, NZ). Strains may originate from genetic resources and repositories: American Type Culture Collection, 10801 University Blvd., Manassas, VA 20110-2209, USA (strains prefixed with ATCC); CABI Europe - International Mycological Institute, Bakeham Lane, Egham, Surrey, TW20 9TYNRRL, UK(strains with the prefixes CABI and IMI); Centraalbureau voor Schimmelcultures, Fungal Biodiversity Centre, Uppsalaan 8, PO Box 85167, 3508 AD Utrecht, The Netherlands (strains with the prefix CBS); Division of Plant Industry, CSIRO, Canberra, Australia (strains with the prefix CC); Collection Nationale de Cultures de Microorganismes, Institut Pasteur, 25 rue du Docteur Roux, F-75724 PARIS Cedex 15 (strains with the prefix CNCM); Le i bn iz -1 n st i tu t DSMZDeutsche Sammlung von Mikroorganismen und Zellkulturen GmbH, Inhoffenstrasse 7 B, 38124 Braunschweig, Germany (strains with the prefix DSM); International Depositary Authority of Cañada Collection, Canada (strains with the IDAC prefix); International Collection of Micro-organisms from Plants, Landcare Research, Private Bag 92170, Auckland Mail Centre, Auckland 1142, New Zealand (strains with ICMP prefix); UTA, PMB 5320, Ibadan, Nigeria (strains with the prefix UTA); The National Collections of Industrial and Marine Bacteria Ltd., Torry Research Station, PO Box 31, 135 Abbey Road, Aberdeen, AB9 8DG, Scotland (strains with the prefix NCIMB); ARS Culture Collection of the hQRjnn / i znz / E / YiAi. National Center for Agricultural Utilization Research, Agricultural Research Service, United States Department of Agriculture, 1815 North University Street, Peoria, Illinois 61604, USA (strains with the prefix NRRL); Department of Scientific and Industrial Research Culture Collection, Applied Biochemistry Division, Palmerston North, New Zealand (strains with the prefix NZP); FEPAGRO-Fundagão Estadual de Pesquisa Agropecuária, Rua Gongalves Dias, 570, Bairro Menino Deus, Porto Alegre / RS, Brazil (strains with the prefix SEMIA); SARDI, Adelaide, South Australia (strains with the prefix SRDI); United States Department of Agriculture, Agricultural Research Service, Soybean and Alfalfa Research Laboratory, BARC-West, 10300 Baltimore Boulevard, Building 011, Room 19-9, Beltsville, MD 20705, USA (strains with the USDA prefix: Beltsville Rhizobium Culture Collection Catalog, March 1987 USDA-ARS ARS30: http: / / pdf.usaid.gov / pdf_docs / PNAAW891.pdf); and Murdoch University, Perth, Western Australia (strains with the prefix WSM). Other strains can be found in the World Catalogue of Microorganisms: http: / / gcm.wfcc.info / and http: / / www.landcareresearch.co.nz / resources / collections / icmp and other references to strain collections and their prefixes at http: / / refs.wdcm.org / collections.htm. Bacillus amyloliquefaciens subsp. plantarum MBI600 (NRRL B50595) is deposited under accession number NRRL B-50595 with the strain designation Bacillus subtilis 1430 (and is identical to NCIMB 1237). Recently, MBI 600 was reclassified as Bacillus amyloliquefaciens subsp. plantarum hQAJnn / l 7A7 / B / YILI based on a polyphasic test that combines classical microbiological methods using a mixture of traditional tools (such as culture-based methods) and molecular tools (such as fatty acid analysis and genotyping). Therefore, Bacillus subtilis MBI600 (or MBI 600 or MBI600) is identical to Bacillus amyloliquefaciens subsp. plantarum MBI600, formerly Bacillus subtilis MBI600. Bacillus amyloliquefaciens MBI600 is known as a treatment for rice seeds, promoting plant growth from Int. J. Microbiol. Res. 3(2) (201 1), 120-130 and is also described, for example, in US 2012 / 0149571 A1.This MBI600 strain, for example, is commercially available as an INTEGRAL® liquid formulation product (Becker-Underwood Inc., USA). Bacillus subtilis strain FB17 was originally isolated from red beet roots in North America (System Appl. Microbiol 27 (2004) 372-379). This B. subtilis strain promotes phytosanity (US 2010 / 0260735 A1; WO 201 1 / 109395 A2). B. subtilis FB17 was also deposited at ATCC with the number PTA-11857 ​​on April 26, 2011. Bacillus subtilis strain FB17 can also be referred to as UD1022 or UD10-22. Bacillus amyloliquefaciens AP-136 (NRRL B-50614), B. amyloliquefaciens AP-188 (NRRL B-50615), B. amyloliquefaciens AP-218 (NRRL B-50618), B. amyloliquefaciens AP-2 (NRRL B-5019), B. amyloliquefaciens AP-219 (NRRL B-50615). amyloliquefaciens AP-295 (NRRL B-50620), B. japonicum SEMIA 5079 (e.g., Gelfix 5 or Adhere 60 from Nitral Urbana Laboratories, hQAJnn / l 7Π7 / Β / ΥΙΛΙ Brazil, a BASF company), B. japonicum SEMIA 5080 (e.g., GELFIX 5 or ADHERE 60 from Nitral Urbana Laoboratories, Brazil, a BASF company), B. mojavensis AP-209 (NRRL B-50616), B. solisalsi AP-217 (NRRL B-50617), B. pumilus strain INR-7 (also called BU-F22 (NRRL B-50153) and BU-F33 (NRRL B-50185)), B. simplex ABU 288 (NRRL B-50340) and B. amyloliquefaciens subsp. plantarum MBI600 (NRRL B-50595) were mentioned, among others, in US patent application 20120149571, US 8,445,255, WO 2012 / 079073. Bradyrhizobium japonicum USDA 3 is known from US patent 7,262,151. Jasmonic acids or salts (jasmonates) or derivatives include, but are not limited to, potassium jasmonate, sodium jasmonate, lithium jasmonate, ammonium jasmonate, dimethylammonium jasmonate, isopropylammonium jasmonate, diolammonium jasmonate, diettriethanolammonium jasmonate, jasmonic acid methyl ester, jasmonic acid amide, methylamide of jasmonic acid, jasmonic acid-L-amino acid (amide-linked) conjugates (e.g. conjugates with L-isoleucine, L-valine, L-leucine or L-phenylalanine), 12-oxophytodienoic acid, coronatine, coronafacoyl-L-serine, coronafacoyl-L-threonine, methyl esters of 1-oxo-indanoyl-isoleucine, methyl esters of 1-oxo hQA7nn / l 7P7 / E / YILI indanoyl-leucine, coronalon (methyl ester of 2-[(6-ethyl-l-oxo-indan-4carbonyl)-amino]-3-methyl-pentanoic acid), linoleic acid or derivatives thereof and cis-jasmone, or combinations of any of the above. Bilobalide and ginkgolides are known components of the ginkgo tree. Bilobalide is the common name for (3aS,5aR,8aS,9R,10aR)-9-tert-butyl-8,9-dihydroxhydro-9H-furo[2,3b]furo[3',2,;2,3]cyclopenta[1,2-c]furan-2,4,7(3H,8H)-trione (CAS 3357004-6), and the following ginkgolides were also previously described and registered: ginkgolide (CAS 15291-75-5), ginkgolide B (CAS 15291-777), ginkgolide C (15291-76-6), ginkgolide J (15291-79-9), ginkgolide M (15291-78-8). The compounds are commercially available, or can preferably be obtained from ginkgo leaves using methods known in the prior art and described, for example, in US 5,700,468, EP-A 360 556, EP-A 0 431 535 and JP-A 09-1 10713.In addition, the compounds bilobalide (in enantiopure form), ginkgolide A (in its racemic form) and ginkgolide B (in its racemic form) can be obtained by chemical synthesis, as described, for example, in Tetrahedron Letters (1988), 29(28), 3423-6, Tetrahedron Letters (1988), 29(26), 3205-6 and Journal of the American Chemical Society (2000), 122(35), 8453-8463, respectively. Compound III The commercially available compounds of group M listed above can be found in The Pesticide Manual, 15th edition, CDS Tomlin, British Crop Protection Council (2011), among other publications. The neonicotinoid cycloxaprid is known from WO20120 / 069266 and WO2011 / 06946, and the neonicotinoid compound M.4A.2, sometimes also called Guadipyr, is known from WO2013 / 003977, and the neonicotinoid compound M.4A.3 (approved as paichongding in China) is known from WO2010 / 069266. The metaflumizone analogue hQA7nn / l 7P7 / B / YILI M.22B.1 is described in CN 10171577, and the analogue M.22B.2 in CN102126994. Both phthalamides M.28.1 and M.28.2 are known from WO 2007 / 101540. Anthranilamide M.28.3 was described in WO2005 / 077934. Hydrazide compound M 28.4 was described in WO 2007 / 043677. Anthranilamides M.28.5a) to M.28.5h) can be prepared as described in WO 2007 / 006670, WO2013 / 024009 and WO2013 / 024010, anthranilamide compound M.28.5I) is described in WO201 1 / 085575, compound M.28.5j) in WO2008 / 134969, compound M.28.5k) in US201 1 / 046186 and compound M.28.5I) in WO2012 / 034403. Diamide compounds M.28.6 and M.28.7 can be found in CN102613183. The anthranilamide compounds M.28.8a) and M.28.8b) are known from WO2010 / 069502. The quinoline derivative flometoquin is listed in WO2006 / 013896. The aminofuranone compound flupyradifurone is known from WO2007 / 115644. The sulfoximine compound sulfoxaflor is known from WO2007 / 149134. From the pyrethroid group, momfluorothrin is known from US6908945 and heptafluthrin from WO10133098. The oxadiazolone compound methoxadizone can be found in JP13 / 166707. The pyrazole acaricide piflubumide is known from WO2007 / 020986. Isoxazoline compounds were described in the following publications: fluralaner in WO2005 / 085216, afoxolaner in WO2009 / 002809 and WO2011 / 149749, and the compound isoxazoline M.UN.9 in WO2013 / 050317. The pyripyropene derivative afidopyropen was described in WO2006 / 129714. Thioxazafen nematicide was described in WO09023721 and fluopyram nematicide in WO2008126922; mixtures hQA7nn / l 7P7 / B / YILI nematicides comprising flupyram were described in WO2010108616. The compound triflumezopyrim was described in WO2012 / 092115. The spirocetal-substituted cyclic ketoenol derivative M.UN.3 is known from WO2006 / 089633 and the biphenyl-substituted spirocyclic ketoenol derivative M.UN.4 from WO2008 / 06791. Triazoylphenyl sulfide M.UN.5 was described in WO2006 / 043635, and the bacillus firmus-based biological control agents in WO2009 / 124707. Compounds M.UN.6a) to M.UN.6i) listed in M.UN.6 were described in WO2012 / 029672, and compounds M.UN.6j) and M.UN.6k) in WO2013 / 029688. The nematicide compound M.UN.8 was described in WO2013 / 055584, and the pyridalyl-type analogue M.UN.10 in WO2010 / 060379. Carboxamide compounds M.UN.Hb) to M.UN.Hh) can be prepared as described in WO2010 / 018714 and carboxamide M.UN.11i) to M.UN.Hp) as described in WO2010 / 127926. The pyridi 11 i az o I is M.UN.12.a) to M.UN.12.c) are known from WO201 0 / 00671 3, M.UN.12.C) and M.UN.12.d) from WO201 2000896, and M.UN.12.f) to M.UN.12.m) from WO2010129497. The malononitrile compound M.UN.13 was described in WO2009 / 0051 10. Compounds M.UN.14a) and M.UN.14b) are known from WO2007 / 1 01 369. Compound M.UN.15 can be found in WO13192035. The MY group biopesticides were described earlier in the paragraphs on biopesticides (of groups MY and F.XII). Mixtures with biopesticides According to one embodiment of the mixtures of the invention, at least one biopesticide is selected from groups F.XII or bQRynn / i ζπζ / β / υιλι M.Y. According to one embodiment of the mixtures of the invention, at least one biopesticide is selected from group F.XIL According to one embodiment of the mixtures of the invention, at least one biopesticide is selected from group MY-1. According to one embodiment of the mixtures of the invention, at least one biopesticide is selected from MY-2. Preferences The preferred fungicidal active compounds II are selected from group F With regard to their use in the pesticide mixtures of the present invention, compounds C.11, which are listed in the following paragraphs, are particularly preferred. With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.1.1 Most preferably, compound II is azoxystrobin, fluoxastrobin, picoxystrobin, pyraclostrobin, or trifloxystrobin. With maximum preference, compound II is pyraclostrobin. With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.L2 Most preferably, compound II is cyazofamide. With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.L3 Most preferably, compound II is bixafen, boscalid, fluopyram, fluxapyroxad, isopirazam, penflufen, pentiopyrad or sedaxane. Most preferably, compound II is fluxapyroxad. With respect to use in a pesticide mixture of the present invention, compound II is selected from group FI4. Most preferably, compound II is ametoctradin or siltiofam. With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.11.1 Most preferably, compound II is difenoconazole, epoxiconazole, fluquinconazole, flusilazole, flutriafol, ipconazole, metconazole, prothioconazole, tebuconazole, triticonazole, or prochloraz. With greater preference, compound II is selected from the group consisting of 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1 (1,2,4-triazol-1 yl)pentan-2-ol, 1 - [4-(4-chlorophenoxy)-2-(trifluoromethl)-1¡¡l cyclopropyl-2(1,2,4-triazol-1 -yl)ethanol, 2-[4-(4-chlorophenoxy)-2-(trifluorometh¡l)phen¡l]-1 (1,2,4-triazol-1 - yl)butan-2-ol, 2-[2-chloro-4-(4-chlorophenyl) -(1,2,4triazol-1 - yl)butan-2-ol, 2-[4-(4-chlorophenoxy)-2-(tnfluoromet¡l)phenyl]-3-met¡l1 - (1,2,4-triazol-1 - yl)butan-2-ol, 2-[4-(4-chlorophenoxy¡)-2(trifluoromethyl)-phenyl]-1-(1,2,4-tr iaz ol -1 - yl)propane - 2-o 1, 2-[2-chloro-4-(4chlorophenoxy)phenyl]-3-methyl-1 - (1,2,4-triol-2-ylbutan) 2-[4-(4chlorophenoxy)-2-(trifluoromet¡l)-iffen¡l]-1 - (1,2,4-triazol-1 - yl)pentan-2-ol o 2[4-(4-f luoroph en oxy)-2-(triflu orom ethyl)-phenyl]-1 - (1,2,4,4-triolpropane-1-2). Preferably, compound II is 2-[2-chloro-4-(4chlorophenoxy)phenyl]-1 (1,2,4-tri azo I -1 -yl)pentan-2-ol. Most preferably, compound II is 1-[4-(4-chlorophenoxy¡)-2hQAJnn / l 7Π7 / Β / ΥΙΛΙ (trifluoromethyl)phen¡l]-1 cyclopropi 1-2-(1,2,4-triazol-1 - i I) ethane or I With highest preference, compound II is 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triaz or 1-1-yl)butan-2-ol With maximum preference, compound II is 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1,2,4-triazol-1-yl)butan-2-ol With maximum preference, compound II is 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-3-methyl-1-(1,2,4-triazol-1-yl)butan-2-ol. With maximum preference, compound II is 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triaz or I-1-yl)butan-2-ol. With maximum preference, compound II is 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-3-methyl-1-(1,2,4-triazol-1-yl)butan-2-ol. With maximum preference, compound II is 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triaz or I-1-yl)pentan-2-ol. With maximum preference, compound II is 2-[4-(4-fluorophenoxy)2-(trifluoromethyl)phenyl]-1-(1,2,4-triazo-1-yl)propan-2-ol. With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.11.2 With respect to use in a pesticide mixture of the present invention, compound II is selected from group F.III. 1 Most preferably, compound II is metalaxyl and mefenoxam (metalaxyl-M). With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.111.2 With respect to use in a pesticide mixture of the present invention, compound II is selected from group F.IV.1 hQRjnn / i znz / E / YiAi Most preferably, compound II is benomyl, carbendazim, and thiophanate-methyl. With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.IV.2 Preferably, compound II is etaboxam, fluopicolide, or pyriophenone. With regard to use in a pesticide mixture of the present invention, compound II is selected from group FV1 With regard to use in a pesticide mixture of the present invention, compound II is selected from group FV2 With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.VL1 With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.VI.2 With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.VI1.1 With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.VIL2 With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.VIL3 Most preferably, compound II is dimethomorph. With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.VIL4 With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.VI11.1 hQA7nn / l 7Π7 / Β / YILI Most preferably, compound II is sulfur. Preferably, compound II is a copper salt selected from copper acetate, copper hydroxide, copper oxychloride, or basic copper sulfate. With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.VIII.2 Preferably, compound II is mancozeb, metiram, or propineb. With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.VIII.3 With greater preference, compound II is the or rotal oni I. With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.VIII.4 With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.IX) With respect to use in a pesticide mixture of the present invention, compound II is selected from group FX). Most preferably, compound II is phosphorous acid or its salts. With regard to use in a pesticide mixture of the present invention, compound II is selected from group F.XI). Pesticide mixtures containing azoxystrobin as compound II are especially preferred. Pesticide mixtures containing fluoxastrobin as compound II are especially preferred. hQB7nn / i znz / E / YiAi Picoxystrobins are especially preferred as compound II. Pyraclostrobin is especially preferred as compound II. Trifluoroxystrobins are especially preferred as compound II. Cyazofamides are especially preferred as compound II. Bixafen is especially preferred as compound II. Boscalids are especially preferred as compound II. Fluopyrams are especially preferred as compound II. Fluxapyroxad is especially preferred as compound II. Isopirazam is especially preferred as compound II. Penflufen is especially preferred as compound II. Pentiopyrads are especially preferred as compound II. Sedaxane is especially preferred as compound II. Pesticide mixtures containing ametoctradin as compound II are especially preferred. Pesticide mixtures containing the compound siltiofam as compound II are especially preferred. Pesticide mixtures containing oxati api pro I in as compound II are particularly preferred. Pesticide mixtures containing epoxiconazole as compound II are particularly preferred. hQRjnn / ι znz / E / YiAi Difenoconazole is especially preferred as compound II. Fluquinconazole is especially preferred as compound II. Flutriafol is especially preferred as compound II. Flusilazoles are especially preferred as compound II. Ipconazole is especially preferred as compound II. Metconazole is especially preferred as compound II. Prothioconazole is especially preferred as compound II. Tebuconazole is especially preferred as compound II. Triticonazoles are especially preferred as compound II. Pesticide mixtures containing cyproconazole as compound II are especially preferred. Pesticide mixtures containing triadimenol as compound II are particularly preferred. Pesticide mixtures containing epoxiconazole as compound II are particularly preferred. Pesticide mixtures containing fludioxonil as compound II are especially preferred. Pesticide mixtures containing the compound metalaxyl as compound II are especially preferred. Pesticide mixtures containing the compound mefenoxam (metalaxyl-M) as compound II are especially preferred. Pesticide mixtures containing thiabendazole as compound II are particularly preferred. Pesticide mixtures containing benomyl as compound II are especially preferred. Pesticide mixtures containing the compound carbendazim as compound II are especially preferred. Pesticide mixtures containing the compound thiophanate-methyl as compound II are particularly preferred. Pesticide mixtures containing etaboxam as compound II are especially preferred. Pesticide mixtures containing fluopicolide as compound II are particularly preferred. Pesticide mixtures containing hQA7nn / l 7P7 / E / YILI pyrophenone as compound II are particularly preferred. Pesticide mixtures containing valifenalate as compound II are particularly preferred. Pesticide mixtures containing dimethomorph as compound II are particularly preferred. Pesticide mixtures containing thiram as compound II are especially preferred. Pesticide mixtures containing ziram as compound II are especially preferred. Pesticide mixtures containing the copper salt compound as compound II are especially preferred. Pesticide mixtures containing sulfur as compound II are especially preferred. Pesticide mixtures containing the compound mancozeb as compound II are especially preferred. Pesticide mixtures containing the compound metiram as compound II are especially preferred. Pesticide mixtures containing the compound propineb as compound II are especially preferred. Pesticide mixtures containing the compound chlorothalonil as compound II are particularly preferred. Pesticide mixtures containing phosphorous acid as compound II are especially preferred. The preferred insecticidal active compounds III are selected from group M With regard to their use in the pesticide mixtures of the present invention, the active compounds II listed in the following paragraphs are of particular preference: hQAJnn / l 7Π7 / Β / YΙΛΙ The preferred combinations are those that additionally include as active ingredient III an active insecticide compound selected from the group that consists of fipronil, chlorfenapir, thiodicarb, lambacialotrin, alpha-cypermethrin, acetamiprid, clothianidin, dinotefuran, imidacloprid, thiacloprid, thiamethoxam, abamectin, emamectin, flubendiamida, espinetoram, espirotetramat, sulfoxaflor, cyflumethofeno, flupiradifurona, chlorantraniliprol, N-[4,6-dichloro-2-[(diethyl-lambda-4su lfanilidene)carbamo i I ]-f en il]-2-(3-chloro-2-pyrid¡l)-5-(trif luoromethyl )pyrazol3-carboxamida, N-[4-chloro-2-[(diethyl-lambda-4-sulfan¡l¡den)carbamo¡l]-6methyl-phenyl]-2-(3-chloro-2-pyrid¡l)-5-(tr¡fluoromet¡l)p¡razol-3-carboxam¡da or N-[4-chloro-2-[(di-2-prop¡l-lambda-4-sulfan¡l¡den)carbamo¡l]-6-methyl-phen¡l]2-(3-chloro-2-pyr¡d¡l)-5-(tr¡fluoromet¡l)pyrazol-3-carboxam¡da oc¡ anthran i I ip rol. Most preferably, the addition of fipronil as active ingredient III. The addition of abamectin as active compound III is preferred. The addition of emamectin as active compound III is preferred. The addition of methiocarb as active compound III is preferred. The addition of thiodicarb as active compound III is preferred. The addition of chlorantraniliprole as active compound III is preferred. hQRjnn / i znz / E / YiAi The addition of cyantraniliprole as active compound III is preferred. The addition of flubendiamide as active compound III is preferred. The addition of N-[4,6-dichloro-2-[(diethylammbda-4-sulfanilydene)carbamoyl]-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazol-3-carboxamide as active compound III is preferred. The addition of N-[4-chloro-2-[(diethylammbda-4-sulfanilydene)carbamoyl]-6-methyl-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazol-3-carboxamide as active compound III is preferred. The addition of N-[4-chloro-2-[(di-2-propyllambda-4-sulfanilyden)carbamoyl]-6-methyl-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazol-3-carboxamide as active compound III is preferred. The addition of chlorfenapyr as active compound III is preferred. The addition of acetate as active compound III is preferred. The addition of spinetoram as active compound III is preferred. The addition of spinosad as active compound III is preferred. The addition of spirotetramat as active compound III is preferred. The addition of triflumezopirim as the active ingredient is preferred. III hQA7nn / l 7P7 / B / YILI The addition of sufoxaflor as active compound III is preferred. The addition of chlorpyrifos as active compound III is preferred. The addition of ciflumethophen as active compound III is preferred. The addition of bifenthrin as active compound III is preferred. The addition of flupyradifurone as active compound III is preferred. The addition of tefluthrin as active compound III is preferred. The addition of cypermethrin as active compound III is preferred. The addition of α-cypermethrin as active compound III is preferred. The addition of a neonicotinic compound from group M.4 is preferred. The addition of acetamiprid as active compound III is of highest preference. Also of highest preference is the addition of clothianidin as active compound III. Also of highest preference is the addition of dinotefuran as active compound III. Also of highest preference is the addition of imidacloprid eQRynn / i ζπζ / β / υιλι as active compound III. Also of highest preference is the addition of thiacloprid as active compound III. Also of highest preference is the addition of thiamethoxam as active compound III. Preferred mixtures according to the invention Binary mixtures of the compound of Formula I and a compound II selected from groups F.1 to F.XI are a preferred embodiment of the invention. Ternary mixtures of a compound of Formula I and two compounds II selected from groups F1 to F11 are another embodiment of the invention. Ternary mixtures of the compound of Formula I with a compound II selected from groups F1 to F11 and a compound III selected from groups M1 to M1UNX are another embodiment of the invention. Pests and fungi Mixtures of active compounds I and II, or active compounds I and II used simultaneously, i.e., together or separately, exhibit outstanding action against animal pests and phytopathogenic fungi. The mixtures of the Formula I compound are especially suitable for effectively combating phytopathogenic fungi. The mixtures of the present invention have excellent activity against a broad spectrum of phytopathogenic Ascomycetes fungi, hQRjnnil 7P7 / B / YILI Basidiomycetes, Deuteromycetes, and Peronosporomycetes (syn. Oomycetes). Some of these are systemically effective and can be used for crop protection as foliar fungicides, seed coating fungicides, and soil fungicides. They can also be used to treat seeds. They are particularly important in the control of multiple fungi in various cultivated plants, such as wheat, rye, barley, oats, rice, corn, lawns, bananas, cotton, soybeans, coffee, sugar cane, vines, fruits and ornamental plants, and vegetables, such as cucumbers, beans, tomatoes, potatoes and gourds, and on the seeds of these plants. They are especially suitable for the control of the following plant diseases: Albugo spp. (white rust) on ornamentals, vegetables (e.g., A. candida) and sunflowers (e.g., A. tragopogonis); Alternaria spp. (Alternaria leaf spot) on vegetables, rapeseed (A. brassicola or brassicae), sugar beet (A. tenuis), fruits, rice, soybeans, potatoes (e.g., A. solani or A. alternata), tomatoes (e.g., A. solani or A. alternata) and wheat; Aphanomyces spp. on sugar beet and vegetables; Ascochyta spp. on cereals and vegetables, e.g., A. tritici (anthracnose) on wheat and A. hordei on barley; Bipolaris and Drechslera spp. (teleomorph: Cochliobolus spp.), e.g., Southern leaf blight (D. maydis) or Northern leaf blight (B. zeicola) in corn, for example, leaf spot (B. sorokiniana) in cereals and, for example, B.oryzae in rice and turfgrass; Blumeria (formerly Erysiphe) graminis (powdery mold) in cereals (e.g., wheat or barley); Botrytis cinerea (teleomorph: Botryotinia fuckeliana: gray mold) in fruits and berries (e.g., strawberries), vegetables (e.g., lettuce, carrots, celery, and cabbages), rapeseed, flowers, vines, forest plants, and wheat; Bremia lactucae (downy mildew) in lettuce; Ceratocystis (syn. Ophiostoma) spp. (rot or wilt) in broadleaf evergreen trees, e.g., C. ulmi (Dutch elm disease) in elms; Cercospora spp. (Cercospora leaf spots) in maize (e.g., gray leaf spot: C. zeae-maydis), rice, sugar beet (e.g., C. beticola), sugar cane, vegetables, coffee, soybeans (e.g., C. sojina or C. kikuchii) and rice; Cladosporium spp. in tomatoes (e.g., C. fulvum: leaf mold) and cereals, e.g., C.herbarum (black spike) in wheat; Claviceps purpurea (ergot) in cereals; Cochliobolus (anamorph: Bipolaris Helminthosporium) spp. (leaf spots) on maize (C. carbonum), cereals (e.g. C. sativus, anamorph: B. sorokiniana) and rice (e.g. C. miyabeanus, anamorph: H. oryzae); Colletotrichum (teleomorph: Glomerella) spp. (anthracnose) in cotton (e.g., C. gossypii), maize (e.g., C. graminicola: anthracnose stem rot), soft fruits, potatoes (e.g., C. coccodes: black spot), beans (e.g., C. lindemuthianum) and soybeans (e.g., C. truncatum or C. gloeosporioides), Corticium spp., e.g., C. sasakii (sheath blight) in rice; Corynespora cassiicola (leaf spots) in soybeans and ornamentals; Cycloconium spp., e.g., C. oleaginum in olive trees; Cylindrocarpon spp. (e.g., fruit tree ulcer or young vine deterioration, teleomorph: Nectria or Neonectria spp.) in fruit trees, vines (e.g., C. liriodendri, teleomorph: Neonectria liriodendri: Black Foot Disease) and ornamentals; Dematophora (teleomorph: Rosellinia) necatrix (root and stem rot) in soybeans; Diaporthe spp., e.g., D. phaseolorum (drop) in soybeans; Drechslera (syn. Helminthosporium, teleomorph: Pyrenophora) spp. in maize, cereals such as barley (e.g., D. teres, net blotch) and wheat (e.g., D. tritici-repentis: brown spot), rice and turfgrass; Esca (dieback, apoplexy) in grapevines, caused by Formitiporia (syn. Phellinus) punctata, F. mediterranea, Phaeomoniella chlamydospora (Phaeoacremonium chlamydosporum early), Phaeoacremonium aleophilum and / or Botryosphaeria obtusa; Elsinoe spp. in pome fruits (E. pyri), soft fruits (E. veneta: anthracnose) and vines (E. ampelina: anthracnose); Entyloma oryzae (leaf blight) on rice; Epicoccum spp. (black mold) on wheat; Erysiphe spp.(powdery mold) in sugar beet (E. betae), vegetables (e.g., E. pisi), such as cucurbits (e.g., E. cichoracearum), cabbage, rapeseed (e.g., E. cruciferarum); Eutypa lata (Eutypa ulcer or acronecrosis, anamorph: Cytosporina lata, syn. Libertella blepharis) in fruit trees, vines and ornamental woodlands; Exserohilum (syn. Helminthosporium) spp. in maize (e.g., E. turcicum); Fusarium (teleomorph: Gibberella) spp. (wilting, root or stem rot) in various plants, such as F. graminearum or F. culmorum (root rot, scab or top blight) in cereals (e.g., wheat or barley), F. oxysporum hQRjnnn znz / E / YiAi in tomatoes, F. solani (f. sp. glycines now syn. F. virguliforme) and F. tucumaniae and F. brasiliense, each of which causes sudden death syndrome in soybeans, and F.verticillioides in maize; Gaeumannomyces graminis (take-all) in cereals (e.g., wheat or barley) and maize; Gibberella spp. in cereals (e.g., G. zeae) and rice (e.g., G. fujikuroi: Bakanae disease); Glomerella cingulata in grapevines, pome fruits, and other plants, and G. gossypii in cotton; grain staining complexes in rice; Guignardia bidwellii (black rot) in grapevines; Gymnosporangium spp. in rosaceous plants and junipers, e.g., G. sabinae (rust) in pears; Helminthosporium spp. (syn. Drechslera, teleomorph: Cochliobolus) in maize, cereals, and rice; Hemileia spp., e.g., H. vastatrix (coffee leaf rust) in coffee; Isariopsis clavispora (syn. Cladosporium vitis) in grapevines; Macrophomina phaseolina (syn. phaseoli) (root and stem rot) in soybeans and cotton; Microdochium (syn. Fusarium) nivale (pink snow mold) in cereals (e.g., wheat or barley); Microsphaera diffusa (powdery mold) in soybeans; Monilinia spp., e.g., M.laxa, M. fructicola and M. fructigena (flower and twig blight, brown rot) in stone fruits and other rosaceous plants; Mycosphaerella spp. in cereals, bananas, soft fruits and nuts, such as, for example, M. graminicola (anamorph: Septoria tritici, Septoria spot) in wheat or M. fijiensis (black Sigatoka disease) in bananas; Peronospora spp. (downy mildew) in cabbage (for example, P. brassicae), rapeseed (for example, P. parasitica), onion (for example, P. destructor), tobacco (P. tabacina) and soybean (for example, P. manshurica); hQRjníMl 7Π7 / Β / YΙΛΙ Phakopsora pachyrhizi and P. meibomiae (soybean rust) in soybeans; Phialophora spp., for example, in grapevines (e.g., P. tracheiphila and P. tetraspora) and soybeans (e.g., P. gregata: stem rot); Phoma lingam (root and stem rot) in rapeseed and cabbage, and P. betae (root rot, leaf spot, and drop) in sugar beets; Phomopsis spp. in sunflowers, grapevines (e.g., P. viticola and leaf spot), and soybeans (e.g., stem rot: P. phaseoli, teleomorph: Diaporthe phaseolorum); Physoderma maydis (brown spot) in maize; Phytophthora spp. (wilting, root, leaf, fruit and stem rot) in various plants, such as bell peppers and cucurbits (e.g., P. capsici), soybeans (e.g., P. megasperma, syn. P. sojae), potatoes and tomatoes (e.g., P. infestans: late blight) and broadleaf trees (e.g., P. ramorunr.sudden oak death); Plasmodiophora brassicae (club root) in cabbage, rapeseed, radish and other plants; Plasmopara spp., for example, P. viticola (grapevine downy mildew) in grapevines and P. halstedii in sunflowers; Podosphaera spp. (powdery mildew) in rosaceous plants, hops, pome and soft fruits, for example, P. leucotricha in apple; Polymyxa spp., for example, in cereals such as barley and wheat (P. graminis) and sugar beet (P. betae) and thus virally transmitted diseases; Pseudocercosporella herpotrichoides (eyespot, teleomorph: Tapesia yallundae) in cereals, for example, wheat or barley; Pseudoperonospora (downy mildew) in various plants, for example, P. cubensis in cucurbits or P. humili in hops; Pseudopezicula tracheiphila (disease that causes red color or hQRjnn / i znz / E / YiAi rotbrenner, anamorph: Phialophora) in vines; Puccinia spp. (rusts) in various plants, for example, P. triticina (leaf rust or brown rust), P.striiformis (striped or yellow rust), P. hordei (dwarf rust), P. graminis (stem or black rust) or P. recondita (brown or leaf rust) on cereals, such as, for example, wheat, barley or rye, P. kuehnii (orange rust) on sugar cane and P. asparagi on asparagus; Pyrenophora (anamorph: Drechslera) tritici-repentis (brown spot) on wheat or P. teres (net spot) on barley; Pyricularia spp., for example, P. oryzae (teleomorph: Magnaporthe grísea, rice fungus) on rice and P. grísea on grass and cereals; Pythium spp. (drop) in turf, rice, corn, wheat, cotton, rapeseed, sunflower, soybean, sugar beet, vegetables and various other plants (e.g., P. ultimum or P. aphanidermatum); Ramularia spp., e.g., R. collo-cygni (Ramularia leaf spots, physiological leaf spots) in barley and R. beticola in sugar beet; Rhizoctonia spp.in cotton, rice, potato, turf, corn, rapeseed, potato, sugar beet, vegetables and various other plants, for example, R. solani (root and stem rot) in soybeans, R. solani (sheath blight) in rice or R. cerealis (Rhizoctonia spring blight) in wheat or barley; Rhizopus stolonifer (black mold, mild rot) in strawberries, carrots, cabbages, vines and tomatoes; Rhynchosporium secalis (scald) in barley, rye and triticale; Sarocladium oryzae and S. attenuatum (sheath rot) in rice; Sclerotinia spp. (stem rot or white mold) in vegetables and field crops, such as rapeseed, sunflower (for example, S. sclerotiorum) and soybeans (for example, S. rolfsii or S. sclerotiorum); Septoria hQRjnnil 7Π7 / Β / ΥΙΛΙ spp. in several plants, for example, S. glycines (brown spot) in soybeans, S. tritici (Septoria spot) in wheat and S. (syn. Stagonospora) nodorum (Stagnospora spot) in cereals; Uncinula (syn.Erysiphe necator (powdery mildew, anamorph: Oidium tuckeri) on vines; Setospaeria spp. (leaf blight) on maize (e.g., S. turcicum, syn. Helminthosporium turcicum) and turfgrass; Sphacelotheca spp. (sow) on maize (e.g., S. reiliana: topsow), sorghum, and sugarcane; Sphaerotheca fuliginea (powdery mildew) on cucurbits; Spongospora subterranea (powdery scab) on potatoes and thus virally transmitted diseases; Stagonospora spp. on cereals, e.g., S. nodorum; Stagonospora, teleomorph: Leptosphaeria [syn. Phaeosphaeria] nodorum) on wheat; Synchytrium endobioticum in potato (potato wart disease); Taphrina spp., for example, T. deformans (leaf curl disease) in peach and T. pruni (plum pit) in plums; Thielaviopsis spp. (black root rot) in tobacco, pome fruits, vegetables, soybeans and cotton, for example, T. basicola (syn. Chalara elegans); Tilletia spp.(common smut or stinking soot) on cereals, such as T. tritici (syn. T. caries, wheat smut) and T. controversa (dwarf smut) on wheat; Typhula incarnata (grey snow mold) on barley or wheat; Urocystis spp., for example, U. occulta (stem soot) on rye; Uromyces spp. (rust) on vegetables, such as beans (for example, U. appendiculatus, syn. U. phaseoli) and sugar beet (for example, U. betae); Ustilago spp. (loose soot) on cereals (for example, U. nuda and U. avaenae), maize (for example, U. maydis: corn soot) and sugar cane; Venturia spp. (scab) on apples (for example, I.L. inaequalis) and pears; and Verticillium spp. (wilt) in various plants, such as fruits and ornamentals, vines, soft fruits, vegetables and field crops, for example, 1 / . dahliae in strawberries, rapeseed, potatoes and tomatoes. The mixtures of the Formula I compound are also suitable for effectively combating animal pests of the following orders: insects of the order of Lepidoptera, for example, Achroia grisalla, Acleris spp., such as A. fimbriana, A. gloverana, A. variaría; Acrolepiopsis assectella, Acronicta major, Adoxophyes spp., such as A. cyrtosema, A. orana; Aedia leucomelas, Agrotis spp., such as A. exclamation, A. fucosa, A. ípsilon, A. orthogoma, A. segetum, A. subterranea; Alabama argillacea, Aleurodicus dispersus, Alsophila pometaria, Ampelophaga rubiginosa, Amyelois transitella, Anacampsis sarcitella, Anagasta kuehniella, Anarsia lineatella, Anisota senatoria, Antheraea pernyi, Anticarsia (=Thermesia) spp., such as A. gemmatalis; Apamea spp., Aproaerema modicella, Archips spp., such as A. argyrospila, A. fuscocupreanus, A. rosana, A. xyloseanus; Argyresthia conjugella, Argyroploce spp., Argyrotaenia spp., such as A. velutinana; Athetis mindara, Austroasca viridigrisea, Autographa gamma, Autographa nigrisigna, Barathra brassicae, Bedellia spp., Bonagota salubricola, Borbo cinnara, Bucculatrix thurberiella, Bupalus piniarius, Busseola spp., Cacoecia spp., tales como C. murinana, C. podana; Cactoblastis cactorum, Cadra cautella, Calingo braziliensis, Caloptilis theivora, Capua reticulana, Carposina spp., tales como C. niponensis, C. sasakii;. hQRjníMl 7Π7 / Β / ΥΙΛΙ Cephus spp., Chaetocnema aridula, Cheimatobia brumata, Chilo spp., such as C. indicas, C. suppressalis, C. partellus; Choreutis pariana, Choristoneura spp., such as C. conflictana, C. fumiferana, C. longicellana, C. murinana, C. occidentalis, C. rosaceana; Chrysodeixis (=Pseudoplusia) spp., such as C. eriosoma, C. includens; Cirphis unipuncta, Clysia ambiguella, Cnaphalocerus spp., Cnaphalocrocis medinalis, Cnephasia spp., Cochylis hospes, Coleophora spp., Colias eurytheme, Conopomorpha spp., Conotrachelus spp., Copitarsia spp., Corcyra cephalonica, Crambus caliginosellus, Crambus teterrellus, Crocidosema (=Epinotia) aporema, Cydalima (=Diaphania) perspectalis, Cydia (=Carpocapsa) spp., such as C. pomonella, C. latiferreana; Dalaca noctuides, Datana integerrima, Dasychira pinícola, Dendrolimus spp., such as D. pini, D. spectabilis, D. sibiricus; Desmia funeralis, Diaphania spp., such as D. nitidalis, D.hyalinata; Diatraea grandiosella, Diatraea saccharalis, Diphthera festiva, Earias spp., such as E. insulana, E. vittella; Ecdytolopha aurantianu, Egira (=Xylomyges) curialis, Elasmopalpus lignosellus, Eldana saccharina, Endopiza viteana, Ennomos subsignaria, Eoreuma loftini, Ephestia spp., such as E. cautella, E. elutella, E. kuehniella; Epinotia aporema, Epiphyas postvittana, Erannis tiliaria, Erionota thrax, Etiella spp., Eulia spp., Eupoecilia ambiguella, Euproctis chrysorrhoea, Euxoa spp., Evetria bouliana, Faronta albilinea, Feltia spp., subterrane, F. comoan; Gallery mellonella, Graduaría spp., Grapholita spp., such as G. funebrana, G. molesta, G. inopinata; Halysidota spp., Harrisina americana, Hedylepta spp., Helicoverpa spp., such as H. armígera hQRjníMl 7Π7 / Β / ΥΙΛΙ (=Heliothis armígera), H. zea (=Heliothis zea); Heliothis spp., such as H. assulta, H. subflexa, H. virescens; Hellula spp., such as H. undalis, H.rogatalis; Helocoverpa gelotopoeon, Hemileuca oliviae, Herpetogramma licarsisalis, Hibernia defoliaria, Hofmannophila pseudospretella, Homoeosoma electellum, Homona magnánima, Hypena scabra, Hyphantria cunea, Hyponomeuta padella, Hyponomeuta malinellus, Kakivoria flavofasciata, Keiferia lycopersicella, Lambdina fiscellaria, Lambdina fiscellaria lugubrosa, Lamprosema indicata, Laspeyresia molesta, Leguminivora glycinivorella, Lerodea eufala, Leucinodes orbonalis, Leucoma salicis, Leucoptera spp., such as L. coffeella, L. scitella; Leuminivora lycinivorella, Lithocolletis blancardella, Lithophane antennata, Llattia octo (=Amyna axis), Lobesia botrana, Lophocampa spp., Loxagrotis albicosta, Loxostege spp., such as L. sticticalis, L. cereralis; Lymantria spp., such as L. dispar, L. monacha; Lyonetia clerkella, Lyonetia prunifoliella, Malacosoma spp., such as M. americanum, M. californicum, M. constrictum, M. neustria; Mamestra spp., such as M. brassicae, M.configure it; Mamstra brassicae, Manduca spp., such as M. quinquemaculata, M. sexta; Marasmia spp., Marmara spp., Maruca testulalis, Megalopyge lanata, Melanchra picta, Melanitis leda, Mocis spp., such as M. lapites, M. repanda; Mocis latipes, Monochroa fragariae, Mythimna separata, Nemapogon cloacella, Neoleucinodes elegantalis, Nepytia spp., Nymphula spp., Oiketicus spp., Omiodes indicata, Omphisa anastomosalis, Operophtera brumata, Orgyia pseudotsugata, Oria spp., Orthaga thyrisalis, Ostrinia spp., such as O. nubilalis; Oulema bQR / nn / l 7Π7 / Β / ΥΙΛΙ oryzae, Paleacrita vernata, Panolis flammea, Parnara spp., Papaipema nebris, Papilio cresphontes, Paramyelois transitella, Paranthrene regalis, Paysandisia archon, Pectinophora spp., such as P. gossypiella; Peridroma saucia, Perileucoptera spp., such as P. coffeella; Phalera bucephala, Phryganidia californica, Phthorimaea spp., such as P. operculella; Phyllocnistis citrella, Phyllonorycter spp., such as P.blancardella, P. crataegella, P. issikii, P. ringoniella; Pieris spp., such as P. brassicae, P. rapae, P. napi; Pilocrocis tripunctata, Plathypena scabra, Platynota spp., such as P. flavedana, P. idaeusalis, P. stultana; Platyptilia carduidactyla, Plebejus argus, Plodia interpunctella, Plusia spp., Plutella maculipennis, Plutella xylostella, Pontia protodica, Prays spp., Prodenia spp., Proxenus lepigone, Pseudaletia spp., such as P. sequax, P. unipuncta; Pyrausta nubilalis, Rachiplusia nu, Richia albicosta, Rhizobius ventralis, Rhyacionia frustrana, Sabulodes aegrotata, Schizura concinna, Schoenobius spp., Schreckensteinia festaliella, Scirpophaga spp., such as S. incertulas, S. innotata; Scotia segetum, Sesamia spp., such as S. inferens, Seudyra subflava, Sitotroga cerealella, Sparganothis pilleriana, Spilonota lechriaspis, S. ocellana, Spodoptera (=Lamphygma) spp., such as S. eridania, S. exigua, S. frugiperda, S. latisfascia, S. littoralis, S. litura, S.omithogalli; Stigmella spp., Stomopteryx subsecivella, Strymon bazochii, Sylepta derogata, Synanthedon spp., such as S. exitiosa, Teda solanivora, Telehin licus. Thaumatopoea pityocampa, Thaumatotibia (=Cryptophlebia) leucotreta, Thaumatopoea pityocampa, Thecla spp., Theresimima ampelophaga, Thyrinteina spp, hQA7nn / l 7Π7 / Β / ΥΙΛΙ. Tildenia inconspicuella, Tinea spp., such as T. cloacella, T. pellionella; Tineola bisselliella, Tortrix spp., such as T. viridana; Trichophaga tapetzella, Trichoplusia spp., such as T. ni; Tuta (=Scrobipalpula) absoluta, Udea spp., such as U. rubigalis, U. rubigalis; Virachola spp., Yponomeuta padella, and Zeiraphera canadensis; insects of the order Coleoptera, for example, Acalymma vittatum, Acanthoscehdes obtectus, Adoretus spp., Agelastica alni, Agrilus spp., such as A. anxius, A. planipennis, A. sinuatus; Agriotes spp., such as A. fuscicollis, A. lineatus, A. obscurus; Alphitobius diaperinus, Amphimallus solstitialis, Anisandrus dispar, Anisoplia austríaca, Anobium punctatum, Anómala corpulenta, Anómala rufocuprea, Anoplophora spp., such as A. glabripennis; Anthonomus spp., such as A. eugenii, A. grandis, A. pomorum; Anthrenus spp., Aphthona euphoridae, Apion spp., Apogonia spp., Athous haemorrhoidalis, Atomaria spp., such as A. linearis; Attagenus spp., Aulacophora femoralis, Blastophagus piniperda, Blitophaga undata, Bruchidius obtectus, Bruchus spp., such as B. lentis, B. pisorum, B. rufimanus; Byctiscus betulae, Callidiellum rufipenne, Callopistria floridensis, Callosobruchus chinensis, Cameraria ohridella, Cassida nebulosa, Cerotoma trifúrcate, Cetonia aurata, Ceuthorhynchus spp., such as C. assimilis, C. napi; Chaetocnema tibialis, Cleonus mendicus, Conoderus spp., such as C. vespertinus; Conotrachelus nenuphar, Cosmopolites spp., Costelytra zealandica, Crioceris asparagi, Cryptolestes ferrugineus, Cryptorhynchus lapathi, Ctenicera spp., such as C. destructor; Curculio spp., Cylindrocopturus spp., Cyclocephala spp., hQRjníMl 7Π7 / Β / ΥΙΛΙ. Dactylispa balyi, Dectes texanus, Dermestes spp., Diabrotica spp., such as D. undecimpunctata, D. speciosa, D. longicornis, D. semipunctata, D. virgifera; Diaprepes abbreviates, Dichocrocis spp., Dicladispa armígera, Diloboderus abderus, Diocalandra frumenti (Diocalandra stigmaticollis), Enaphalodes rufulus, Epilachna spp., such as E. varivestís, E. vigintioctomaculata; Epitrix spp., such as E. hirtipennis, E. similaris; Eutheola humilis, Eutinobothrus brasiliensis, Faustinus cubae, Gibbium psylloides, Gnathocerus cornutus, Hellula undalis, Heteronychus arator, Hylamorpha elegans, Hylobius abietis, Hylotrupes bajulus, Hypera spp., such as H. brunneipennis, H. postica; Hypomeces squamosus, Hypothenemus spp., Ips typographus, Lachnosterna consanguínea, Lasioderma serricorne, Latheticus oryzae, Lathridíus spp., Lema spp., such as L. bilineata, L. melanopus; Leptinotarsa ​​spp., such as L.decemlineata; Leptispa pygmaea, Limonius californicus, Lissorhoptrus oryzophilus, Lixus spp., Luperodes spp., Lyctus spp., such as L. bruneus; Liogenys fuscus , Macrodactylus spp., such as M. subspinosus; Maladera matrida, Megaplatypus mutates, Megascelis spp., Melanotus communis, Meligethes spp., such as M. aeneus; Melolontha spp., such as M. hippocastani, M. melolontha; Metamasius hemipterus, Microtheca spp., Migdolus spp., such as M. fryanus, Monochamus spp., such as M. alternatus; Naupactus xanthographus, Niptus hololeucus, Oberia brevis, Oemona hirta, Oryctes rhínoceros, Oryzaephilus surinamensis, Oryzaphagus oryzae, Otiorrhynchus sulcatus, Otiorrhynchus ovatus, Otiorrhynchus sulcatus, Oulema melanopus, Oulema oryzae, Oxycetonia hQRjníMl 7Π7 / Β / ΥΙΛΙ jucunda, Phaedon spp., such as P. brassicae, P. cochleariae; Phoracantha recurva, Phyllobius pyri, Phyllopertha hortícola, Phyllophaga spp., such as P. helleri; Phyllotreta spp., such as P. chrysocephala, P.nemorum, P. striolata, P. vittula; Phyllopertha horticola, Popillia japonica, Premnotrypes spp., Psacothea hilaris, Psylliodes chrysocephala, Prostephanus truncales, Psylliodes spp., Ptinus spp., Pulga saltona, Rhizopertha dominica, Rhynchophorus spp., such as R. billineatus, R. ferrugineus, R. palmarum, R. phoenicis, R. vulneratus; Saperda candida, Scolytus schevyrewi, Scyphophorus acupunctatus, Sitona lineatus, Sitophilus spp., such as S. granaría, S. oryzae, S. zeamais; Sphenophorus spp., such as S. levis; Stegobium paniceum, Sternechus spp., such as S. subsignatus; Strophomorphus ctenotus, Symphyletes spp., Tanymecus spp., Tenebrio molitor, Tenebrioides mauretanicus, Tribolium spp., such as T. castaneum; Trogoderma spp., Tychius spp., Xylotrechus spp., such as X. pyrrhoderus; and Zabrus spp., such as Z. tenebrioides;. insects of the order Diptera, for example, Aedes spp. such as A. aegypti, A. albopictus, A. vexans; Anastrepha ludens, Anopheles spp., such as A. albimanus, A. crucians, A. freeborni, A. gambiae, A. leucosphyrus, A. maculipennis, A. minimus, A. quadrimaculatus, A. sinensis; Bactrocera invadens, Bibio hortulanus, Calliphora erythrocephala, Calliphora vicina, Ceratitis capitata, Chrysomyia spp., such as C. bezziana, C. hominivorax, C. macellaria; Chrysops atlanticus, Chrysops discalis, Chrysops silacea, Cochliomyia spp., such as C. hominivorax; Contarinia spp., such as C. sorghicola; bQR / nn / l 7Π7 / Β / ΥΙΙΛΙ Cordylobia anthropophaga, Culex spp., such as C. nigripalpus, C. pipiens, C. quinquefasciatus, C. tarsalis, C. tritaeniorhynchus; Culicoides furens, Culiseta inornata, Culiseta melanura, Cuterebra spp., Dacus cucurbitae, Dacus oleae, Dasineura brassicae, Dasineura oxycoccana, Delia spp., such as D. antique, D. coarctata, D. platura, D. radicum; Dermatobia hominis, Drosophila spp., such as D. suzukii, Fannia spp., such as F. canicularis; Gastraphilus spp., such as G. intestinalis; Geomyza tipunctata, Giossina spp., such as G. fuscipes, G. morsitans, G. paipalis, G. tachinoides; Haematobia irritaos, Haplodiplosis equestris, Hippelates spp., Hylemyia spp., such as H. platura; Hypoderma spp., such as H. lineata; Hyppobosca spp., Hydrellia philippina, Leptoconops torrents, Liriomyza spp., such as L. sativae, L. trifolii; Lucilia spp., such as L. caprina, L. cuprina, L. sericata; Lycoria pectoralis, Mansonia titillanus, Mayetiola spp., such as M.destructor; Musca spp., such as M. autumnalis, M. domestica; Muscina stabulans, Oestrus spp., such as O. ovis; Opomyza florum, Oscinella spp., such as O. frit; Orseolia oryzae, Pegomya hysocyami, Phlebotomus argentipes, Phorbia spp., such as P. antiqua, P. brassicae, P. coarctata; Phytomyza gymnostoma, Prosimulium mixtum, Psila rosae, Psorophora columbiae, Psorophora discolor, Flhagoletis spp., such as R. cerasi, R. cingulate, R. indifferens, R. mendax, R. pomonella; Rivellia quadrifasciata, Sarcophaga spp., such as S. haemorrhoidalis; Simulium vittatum, Sitodiplosis mosellana, Stomoxys spp., such as S. calcitrans; Tabanus spp., such as T. atratus, T. bovinus, T. lineola, T. similis;. hQRjnnn znz / E / YiAi Tannia spp., Thecodiplosis japonensis, Típula olerácea, Típula paludosa and Wohlfahrtia spp; insects of the order Thysanoptera, for example, Baliothrips biformis, Dichromothrips corbetti, Dichromothrips ssp., Echinothrips americanus, Enneothrips flavens, Frankliniella spp., such as F. fusca, F. occidentalis, F. tritici; Heliothrips spp., Hercinothrips femoralis, Kakothrips spp., Microcephalothrips abdominalis, Neohydatothrips samayunkur, Pezothrips kellyanus, Rhipiphorothrips cruentatus, Scirtothrips spp., such as S. citri, S. dorsalis, S. perseae; Stenchaetothrips spp., Taeniothrips cardamoni, Taeniothrips inconsequens, Thrips spp., such as T. imagines, T. hawaiiensis, T. oryzae, T. palmi, T. parvispinus, T. tabaco; insects of the order Hemiptera, for example, Acizzia jamatonica, Acrosternum spp., such as A. hilare; Acyrthosipon spp., such as A. onobrychis, A. pisum; Adelges laricis, Adelges tsugae, Adelphocoris spp.,, such as A. rapidus, A. superbus; Aeneolamia spp., Agonoscena spp., Aulacorthum solani, Aleurocanthus woglumi, Aleurodes spp., Aleurodicus disperses, Aleurolobus barodensis, Aleurothrixus spp., Amrasca spp., Anasa tristis, Antestiopsis spp., Anuraphis cardui, Aonidiella spp., Aphanostigma piri, Aphidula nasturtii, Aphis spp., such as A. craccivora, A. fabae, A. forbesi, A. gossypii, A. grossulariae, A. maidiradicis, A. pomi, A. sambucí, A. schneideri, A. spiraecola; Arboridia apicalis, Arilus critatus, Aspidiella spp., Aspidiotus spp., Atanus spp., Aulacaspis yasumatsui, Aulacorthum solani, Bactericera cockerelli (Paratrioza cockerelli), Bemisia spp., such as B. argentifolii, B. tabaci bQRjnnil 7Α7 / Β / ΥΙΛΙ (Aleurodes tabaci); Blissus spp., such as B.leucopterus; Brachycaudus spp., such as B. cardui, B. helichrysi, B. persicae, B. prunicola; Brachycolus spp., Brachycorynella asparagi, Brevicoryne brassicae, Cacopsylla spp., such as C. fulguralis, C. pyricola (Psylla piri); Calligypona marginata, Calocoris spp., Campylomma lívida, Capitophorus horni, Carneocephala fulgida, Cavelerius spp., Ceraplastes spp., Ceratovacuna lanígera, Ceroplastes ceriferus, Cerosipha gossypii, Chaetosiphon fragaefolii, Chionaspis tegalensis, Chlorita onukii, Chromaphis juglandicola, Chrysomphalus ficus, Cicadulina mbila, Cimex spp., such as C. hemipterus, C. lectularius; Coccomytílus halli, Coccus spp., such as C. hesperidum, C. pseudomagnoliarum; Corythucha arcuata, Creontiades dilutus, Cryptomyzus ribis, Chrysomphalus aonidum, Cryptomyzus ribis, Ctenarytaina spatulata, Cyrtopeltis notatus, Dalbulus spp., Dasynus piperis, Dialeurodes spp., such as D. citrifolii; Dalbulus maidis, Diaphorina spp., such as D. citri; Diaspis spp., such as D. bromeliae; Dichelops furcatus, Diconocoris hewetti, Doralis spp., Dreyfusia nordmannianae, Dreyfusia piceae, Drosicha spp., Dysaphis spp., such as D. plantaginea, D. pyri, D. radicóla; Dysaulacorthum pseudosolani, Dysdercus spp., such as D. cingulatus, D. intermedius; Dysmicoccus spp., Edessa spp., Geocoris spp., Empoasca spp., such as E. fabae, E. solana; Epidiaspis leperii, Eriosoma spp., such as E. lanigerum, E. pyricola; Erythroneura spp., Eurygaster spp., such as E. integriceps; Euscelis bilobatus, Euschistus spp., such as E. heros, E. impictiventris, E. servus; Fiorinia teae, Geococcus coffeae, Glycaspis brimblecombei, hQAJnn / l 7Π7 / Β / ΥΙΛΙ. Halyomorpha spp., such as H. halys; Heliopeltis spp., Homalodisca vitripennis (=H. coagulata), Hordas nobilellus, Hyalopterus pruni, Hyperomyzus lactucae, Icerya spp., such as I. purchase; Idiocerus spp., Idioscopus spp., Laodelphax striatellus, Lecanium spp., Lecanoideus floccissimus, Lepidosaphes spp., such as L. ulmi; Leptocorisa spp., Leptoglossus phyllopus, Lipaphis erysimi, Lygus spp., such as L. hesperus, L. lineolaris, L. pratensis; Maconellicoccus hirsutos, Marchalina hellenica, Macropes excavatus, Macrosiphum spp., such as M. rosae, M. avenae, M. euphorbiae; Macrosteles quadrilineatus, Mahanarva fimbriolata, Megacopta cribraria, Megoura viciae, Melanaphis pyrarius, Melanaphis sacchari, Melanocallis (=Tinocallis) caryaefoliae, Metcafiella spp., Metopolophium dirhodum, Moneda costalis, Monedopsis pecanis, Myzocallis coryli, Murgantia spp., Myzus spp., such as M. ascalonicus, M. cerasi, M. nicotianae, M. persicae, M.varians; Nasonovia ribis-nigri, Neotoxoptera formosana, Neomegalotomus spp, Nephotettix spp., such as N. malayanus, N. nigropictus, N. parvus, N. virescens; Nezara spp., such as N. viridula; Nilaparvata lugens, Nysius huttoni, Oebalus spp., such as O. pugnax; Oncometopia spp., Orthezia praelonga, Oxycaraenus hyalinipennis, Parabemisia myricae, Parlatoria spp., Parthenolecanium spp., such as P. corni, P. persicae; Pemphigus spp., such as P. bursarius, P. populivenae; Peregrinos maidis, Perkinsiella saccharicida, Phenacoccos spp., such as P. aceris, P. gossypii; Phloeomyzos passerinii, Phorodon homoli, Phylloxera spp., such as P. devastatrix, Piesma qoadrata, Piezodoros spp., such as P. goildinii; Pinnaspis hQRjníUl 7Π7 / Β / ΥΙΛΙ aspidistrae, Planococcus spp., such as P. citri, P. ficus; Prosapia bicincta, Protopulvinaria pyriformis, Psallus seriatus, Pseudacysta persea, Pseudaulacaspis pentagona, Pseudococcus spp., such as P. comstocki; Psylla spp., such as P. malí; Pteromalus spp., Pulvinaria amygdali, Pyrilla spp., Quadraspidiotus spp.,, such as Q. perniciosus; Quesada gigas, Rastroccus spp., Reduvius senilis, Rhizoecus americanus, Rhodnius spp., Rhopalomyzus ascalonicus, Rhopalosiphum spp., such as R. pseudobrassicas, R. insertum, R. maidis, R. padi; Sagatodes spp., Sahlbergella singularis, Saissetia spp., Sappaphis mala, Sappaphis malí, Scaptocoris spp, Scaphoides titanos, Schizaphis graminum, Schizoneura lanuginosa, Scotinophora spp., Selenaspidus articulatus, Sitobion avenae, Sogata spp., Sogatella furcifera, Solubea insularis, Spissistilus festinus (=Stictocephala festina); Stephanitis nashi, Stephanitis pyrioides, Stephanitis takeyai, Tenalaphara malayensis, Tetraleurodes perseae, Therioaphis macúlate, Thyanta spp., such as T. accerra, T. perditor; Tibraca spp., Tomaspis spp., Toxoptera spp., such as T. aurantii; Trialeurodes spp., such as T. abutilonea, T. ricini, T. vaporariorum; Triatoma spp., Trioza spp., Typhlocyba spp., Unaspis spp., such as U. citri, U. yanonensis; y Viteus of the vine;. insects of the order Hymenoptera, for example, Acanthomyops interjectus, Athalia rosae, Atta spp., such as A. capiguara, A. cephalotes, A. cephalotes, A. laevigata, A. robusta, A. sexdens, A. texana, Bombus spp., Brachymyrmex spp., Camponotus spp., such as C. floridanus, C. pennsylvanicus, C. modoc; Cardiocondyla nuda, hQRjníMl 7Π7 / Β / ΥΙΛΙ Chalibion ​​sp, Crematogaster spp., Dasymutilla occídentalis, Diprion spp., Dolichovespula maculata, Dorymyrmex spp, Dryocosmus kuriphilus, Formica spp, Hoplocampa spp., such as H. minuta, H. testudínea; Iridomyrmex humíHs, Lasius spp., such as L. niger, Linepithema humile, Liometopum spp, Leptocybe invasa, Monomorium spp, such as M. pharaonis, Monomorium, Nylandria fulva, Pachycondyla chinensis, Paratrechina longicornis, Paravespula spp, such as P. germanica, P. pennsylvanica, P. vulgaris; Pheidole spp, such as P. megacephala; Pogonomyrmex spp, such as P. barbatus, P. californicus, Polistes rubiginosa, Prenolepis impairs, Pseudomyrmex gracilis, Schelipron spp, Sirex cyaneus, Solenopsis spp, such as S. gemí nata, S. invicta, S. molesta, S. richteri, S. xyloni, Sphecius speciosus, Sphex spp, Tapinoma spp, such as T. melanocephalum, T. sessile; Tetramorium spp, such as T. caespitum, T. bicarinatum, Vespa spp., such as V. crabro; Vespula spp, such as V.squamosal; Wasmannia auropunctata, Xylocopa sp. insects of the order Orthoptera, for example, Acheta domesticus, Calliptamus italicus, Chortoicetes terminifera, Ceuthophilus spp, Diastrammena asynamora, Dociostaurus maroccanus, Gryllotalpa spp, such as G. africana, G. gryllotalpa; Gryllus spp, Hieroglyphus daganensis, Kraussaria angulifera, Locusta spp., such as L. migratoria, L. pardalina; Melanoplus spp, such as M. bivittatus, M. femurrubrum, M. mexicanus, M. sanguinipes, M. spretus; Nomadacris septemfasciata, Oedaleus senegalensis, Scapteriscus spp, Schistocerca spp, such as S. americana, S. gregaria, Stemopelmatus spp, hQRjnnn znz / E / YiAi Tachycines asynamorus and Zonozerus variegatus; Pests from the class Arachnida, por ejemplo, Acari, por ejemplo, from the families Argasidae, Ixodidae and Sarcoptidae, such as Amblyomma spp. (for example, A. americanum, A. variegatum, A. maculatum), Argas spp., such as A. persicu), Boophilus spp., such as B. annulatus, B. decoloratus, B. microplus, Dermacentor spp, such as D. silvarum, D. andersoni, D. variabilis, Hyalomma spp., such as H. truncatum, Ixodes spp., such as / . ricinus, I. rubicundus, I. scapularis, I. holocyclus, I. pacificus, Rhipicephalus sanguineus, Ornithodorus spp., such as O. moubata, O. hermsi, O. turicata), Ornithonyssus bacoti, Otobius megnini, Dermanyssus gallinae, Psoroptes spp., such as P. ovis, Rhipicephalus spp., such as R. sanguineus, R. appendiculatus, Rhipicephalus evertsi), Rhizoglyphus spp.; Sarcoptes spp., such as S. Scabiei; and the family Eriophyidae, which includes Aceria spp., such as A. sheldoni, A. anthocoptes, Acallitus spp.; Aculops spp., such as A. lycopersici, A.pelekassi; Aculus spp, such as A. schlechtendali; Colomerus vitis, Epitrimerus pyri, Phyllocoptruta oleivora; Eriophytes ribis and Eriophyes spp, such as Eriophyes sheldoni-, the family Tarsonemidae, which includes Hemitarsonemus spp., Phytonemus pallidus and Polyphagotarsonemus latus, Stenotarsonemus spp. Steneotarsonemus spinki; family Tenuipalpidae, which includes Brevipalpus spp., such as B. phoenicis-, the family Tetranychidae, which includes Eotetranychus spp., Eutetranychus spp., Oligonychus spp., Petrobia latens, Tetranychus spp, such as T. cinnabarinus, T. evansi, T. kanzawai, T, pacificus, T. phaseulus, T. telarius and T. urticae; Bryobia praetiosa; Panonychus spp., hQA7nn / l 7Π7 / Β / ΥΙΛΙ such as P. ulmi, P. citri; Metatetranychus spp. y Oligonychus spp., such as O. pratensis, O.perseae), Vasates lycopersici; Fiaoiella indica, the family Carpoglyphidae, which includes Carpoglyphus spp; Penthaleidae spp, such as Halotydeus destructor; the family Demodicidae, with species, such as Demodex spp; the family Trombicidea, which includes Trombicula spp.; the family Macronyssidae, which includes Ornothonyssus spp; the family Pyemotidae, which includes Pyemotes tritici; Tyrophagus putrescentiae; the family Acaridae, which includes Acarus siró; the family Araneida, which includes Latrodectus mactans, Tegenaria agrestis, Chiracanthium sp, Lycosa sp Achaearanea tepidariorum and Loxosceles recusa;. pests of the phylum Nematoda, for example, plant parasitic nematodes, such as root knot nematodes, Meloidogyne spp., such as M. hapla, M. incognita, M. javanica; cyst-forming nematodes, Globodera spp., such as G. rostochiensis; Heterodera spp., such as H. avenae, H. glycines, H. schachtii, H. trifolii; seed agalla nematodes, Anguina spp.; stem and leaf nematodes, Aphelenchoides spp., such as A. besseyi; needle nematodes, Belonolaimus spp., such as B. longicaudatus; pine nematodes, Bursaphelenchus spp., such as B. lignicolus, B. xylophilus; Ring nematodes, Criconema spp.; Criconemella spp., such as C. xenoplax and C. ornata; and, Criconemoides spp., such as Criconemoides informis; Mesocriconema spp.; stem and bulb nematodes, Ditylenchus spp., such as D. destructor, D. dipsaci; lezna nematodes, Dolichodorus spp.; spiral nematodes, Heliocotylenchus multicinctus; sheath and sheathed nematodes, Hemicycliophora spp. and Hemicriconemoides spp.; Hirshmanniella spp.; lanceolate nematodes, Hoploaimus spp.; false root knot nematodes, Nacobbus spp.; needle nematodes, Longidorus spp., such as L. elongatus; damaging nematodes, Pratylenchus spp., such as P. brachyurus, P. neglectus, P. penetraos, P. curvitatus, P. goodeyi; Burrowing nematodes, Radopholus spp., such as R. similis; Rhadopholus spp.; Rhodopholus spp.; Reniform nematodes, Rotylenchus spp., such as R. robustas, R. reniformis; Scutellonema spp.; woody root nematodes, Trichodorus spp., such as T. obtusus, T. primitivus; Paratrichodorus spp., such as P. minor; Stunt nematodes, Tylenchorhynchus spp., such as T. claytoni, T. dubius; Citrus nematodes, Tylenchulus spp., such as T. semipenetrans; dagger nematodes, Xiphinema spp.; and other species of nematodes parasitic on plants; insects of the order Isoptera, for example, Calotermes flavicollis, Coptotermes spp, such as C. formosanus, C. gestroi, C. acinaciformis; Cornitermes cumulans, Cryptotermes spp, such as C. brevis, C. cavifrons; Globitermes sulfureus, Heterotermes spp, such as H. aureus, H. longiceps, H. tenuis; Leucotermes flavipes, Odontotermes spp., Incisitermes spp, such as I. minor, I. Snyder; Marginitermes hubbardi, Mastotermes spp, such as M. darwiniensis Neocapritermes spp, such as N. opacus, N. parvus; Neotermes spp, Procornitermes spp, Zootermopsis spp, such as Z. angusticollis, Z. nevadensis, Reticulitermes spp., such as R. hesperus, R. tibialis, R. speratus, R. flavipes, R. grassei, R. lucifugus, R. santonensis, R. hQRjníMl 7Π7 / Β / ΥΙΛΙ virgin; Termes natalensis, insects of the order of Blattaria, por ejemplo, Blatta spp, such as B. orientalis, B. lateralis; Blattella spp, such as B. asahinae, B. germanica; Leucophaea maderae, Panchlora nivea, Periplaneta spp, such as P. americana, P. australasiae, P. brunnea, P. fuligginosa, P. japónica; Supella longipalpa, Parcoblatta pennsylvanica, Eurycotis floridana, Pycnoscelus surinamensis; insects of the order Siphonoptera, for example, Cediopsylla simples, Ceratophyllus spp., Ctenocephalides spp, such as C. felis, C. canis, Xenopsylla cheopis, Pulex irritans, Trichodectes canis, Tunga penetrans and Nosopsyllus fasciatus; insects of the order of Thysanura, por ejemplo, Lepisma saccharina, Ctenolepisma urbana and Thermobia domestica; plagues of the class Chilopoda, por ejemplo, Geophilus spp., Scutigera spp., such as Scutigera coleoptrata; plagues of the class Diplopoda, por ejemplo, Blaniulus guttulatus, Julus spp, Narceus spp; plagues of the class Symphyla, por ejemplo, Scutigerella immaculata; insects of the order of Dermaptera, por ejemplo, Forfícula auricularia; insects of the order Collembola, for example, Onychiurus spp., such as Onychiurus armatus; pests of the order Isopoda, for example, Armadillidium vulgare, Oniscus asellus, Porcellio scaber; insects of the order Phthiraptera, for example, Damalinia spp., Pediculus spp., such as Pediculus humanus capitis, Pediculus hQRjníMl 7Π7 / Β / ΥΙΛΙ humanus corporis, Pediculus humanus; Pthirus pubis, Haematopinus spp., such as Haematopinus eurysternus, Haematopinus suis; Linognathus spp., such as Linognathus vituli; Bovicola bovis, Menopon gallinae, Menacanthus stramineus and Solenopotes capillatus, Trichodectes spp; Some examples of other species that can be controlled by compounds of Formula (I) include: from the phylum Mollusca, class Bivalvia, for example, Dreissena spp.; class Gastropoda, for example, Arion spp., Biomphalaria spp., Bulinus spp., Deroceras spp., Galba spp., Lymnaea spp., Oncomelania spp., Pomacea canaliclata, Succinea spp.; from the class of helminths, for example, Ancylostoma duodenale, Ancylostoma ceylanicum, Acylostoma braziliensis, Ancylostoma spp., Ascaris lubricoides, Ascaris spp., Brugia mal ay i, Brugia ti morí, Bunostomum spp., Chabertia spp., Clonorchis spp., Cooperia spp., Dicrocoelium spp., Dictyocaulus filaría, Diphyllobothrium latum, Dracunculus medínensis, Echinococcus granulosas, Echinococcus multilocularis, Enterobíos vermicularis, Facióla spp., Haemonchus spp., such as Haemonchus contortus; Heterakis spp., Hymenolepis nana, Hyostrongulus spp., Loa, Nematodirus spp., Oesophagostomum spp., Opisthorchis spp., Onchocerca volvulus, Ostertagia spp., Paragonimus spp., Schistosomen spp., Strongyloides fuelleborni, Strongyloides stercora lis, Stronyloides spp., Taenia saginata, Taenia solium, Trichinella spiralis, Trichinella native, Trichinella britovi, Trichinella nelsoni, Trichinella pseudopsiralis, Trichostrongulus spp., Trichuris trichuria, Wuchereria bancrofti;. hQRjníMl 7Π7 / Β / YΙΛΙ In particular, the mixtures of the present invention are also suitable for effectively combating pests such as insects of the orders Lepidoptera, beetles (Coleoptera), flies and mosquitoes (Diptera), thrips (Thysanoptera), termites (Isoptera), bed bugs, aphids, cicadas, whiteflies, mealybugs, and grasshoppers (Hemiptera), ants, bees, wasps, and sawflies (Hymenoptera), crickets, grasshoppers, and locusts (Orthoptera), and also Arachnoidea, such as arachnids (Acarinha). Formulations The mixtures according to the present invention can be formulated into common formulations, such as solutions, emulsions, suspensions, powders, fine powders, pastes, and granules. The method of use depends on the specific intended purpose; in each case, a fine and uniform distribution of the compounds according to the invention must be ensured. Therefore, the invention also relates to agrochemical compositions comprising an auxiliary and a mixture of at least one compound I of Formula I and at least one compound II (and, optionally, a compound III) according to the present invention. An agrochemical composition comprises an effective amount of compound I as a pesticide. The term "effective amount" indicates a quantity of the composition or of compounds I that is sufficient to control harmful fungi and / or pests in cultivated plants or for the protection of materials, without causing significant damage to the treated plants. This quantity can vary widely and depends on several factors, such as the species of fungi and / or pests to be controlled, the treated material or cultivated plant, climatic conditions, and the specific compound I used. Active compounds I and II (and optionally III), their N-oxides, and salts can be converted into the usual types of agrochemical compositions, for example, solutions, emulsions, suspensions, powders, pastes, granules, pressed products, capsules, and mixtures thereof. Examples of composition types include suspensions (e.g., SC, OD, FS), emulsifying concentrates (e.g., EC), emulsions (e.g., EW, EO, ES, ME), capsules (e.g., CS, ZC), pastes, tablets, moisturizing powders or slurries (e.g., WP, SP, WS, DP, DS), pressed products (e.g., BR, TB, DT), granules (e.g., WG, SG, GR, FG, GG, MG), insecticidal articles (e.g., LN), and gel formulations for treating plant propagation materials such as seeds (e.g., GF). These and other types of compositions are defined in “Catalogue of pesticide formulation types and international coding system”, Technical Monograph No. 2, 6.Edition, May 2008, CropLife International. The compositions are prepared in the known way, as described by Mollet and Grubemann, Formulation technology, Wiley VCH, Weinheim, 2001; or Knowles, New developments in crop protection product formulation, Agrow Reports DS243, T&F Informa, London, 2005. Suitable auxiliaries are solvents, liquid carriers, solid carriers or fillers, surfactants, dispersants, emulsifiers, moisturizers, adjuvants, solubilizers, penetration enhancers, protective colloids, adhesion agents, thickeners, humectants, repellents, attractants, food stimulants, compatibilizers, bactericides, antifreeze, antifoaming agents, colorants, stickiness enhancers and binders. Suitable solvents and liquid carriers include water and organic solvents, such as mineral oil fractions with a medium to high boiling point, e.g., kerosene, diesel fuel; vegetable or animal oils; aliphatic, cyclic, and aromatic hydrocarbons, e.g., toluene, paraffin, tetrahydronaphthalene, alkylated naphthalenes; alcohols, e.g., ethanol, propanol, butanol, benzyl alcohol, cyclohexanol; glycols; DMSO; ketones, e.g., cyclohexanone; esters, e.g., lactates, carbonates, fatty acid esters, gamma-butyrolactone; fatty acids; phosphonates; amines; amides, e.g., N-methylpyrrolidone, fatty acid dimethylamides; and mixtures thereof. Suitable solid carriers or filling agents are mineral earths, for example silicates, silica gels, talc, kaolin, limestone, quicklime, chalk, clay, dolomite, diatomaceous earth, bentonite, calcium sulfate, magnesium sulfate, magnesium oxide; polysaccharides, for example cellulose, starch; fertilizers, for example ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas; products of vegetable origin, for example cereal flour, tree bark flour, wood flour, nut shell flour and mixtures thereof. hQAJnn / l 7Π7 / Β / YΙΛΙ Suitable surfactants are surface-active compounds such as anionic, cationic, nonionic, and amphoteric surfactants, block polymers, polyelectrolytes, and mixtures thereof. These surfactants can be used as emulsifiers, dispersants, solubilizers, wetting agents, penetration enhancers, protective colloids, or adjuvants. Examples of surfactants are listed in McCutcheon's, Vol. 1: Emulsifiers & Detergents, McCutcheon's Directories, Glen Rock, USA, 2008 (International or US edition). Suitable anionic surfactants are alkali, alkaline earth, or ammonium salts of sulfonates, sulfates, phosphates, carboxylates, and mixtures thereof. Examples of sulfonates include alkylaryl sulfonates, diphenyl sulfonates, alpha-olefin sulfonates, lignin sulfonates, fatty acid and oil sulfonates, ethoxylated alkylphenol sulfonates, alkoxylated arylphenol sulfonates, condensed naphthalene sulfonates, dodecylbenzene and tridecylbenzene sulfonates, naphthalene and alkylnaphthalene sulfonates, sulfosuccinates, and sulfosuccinamates. Examples of sulfates include fatty acid and oil sulfates, ethoxylated alkylphenol sulfates, alcohol sulfates, ethoxylated alcohol sulfates, and fatty acid ester sulfates. Examples of phosphates are phosphate esters. Examples of carboxylates are alkyl carboxylates, and carboxylated or ethoxylated alkylphenol alcohols. Suitable nonionic surfactants include alkoxylates, N-substituted fatty acid amides, amine oxides, esters, sugar-based surfactants, polymeric surfactants, and mixtures thereof. Examples of alkoxylates are compounds such as alcohols, alkylphenols, amines, amides, arylphenols, fatty acids, or fatty acid esters that have been alkoxylated with 1 to 50 equivalents. Ethylene oxide and / or propylene oxide can be used for alkoxylation, preferably ethylene oxide. Examples of N-substituted fatty acid amines are fatty acid glucoamides or fatty acid alkanolamides. Examples of esters are fatty acid esters, glycerol esters, or monoglycerides. Examples of sugar-based surfactants include sorbitan, ethoxylated sorbitan, sucrose-glucose esters, and alkyl polyglucosides. Examples of polymeric surfactants include vinylpyrrolidone homopolymers or copolymers, vinyl alcohols, and vinyl acetate. Suitable cationic surfactants are quaternary surfactants, for example, quaternary ammonium compounds with one or two hydrophobic groups or salts of long-chain primary amines. Suitable amphoteric surfactants are alkylbetaines and imidazolines. Suitable block polymers are AB or ABA type block polymers, comprising polyethylene oxide and polypropylene oxide blocks, or ABC type block polymers, comprising alkanol, polyethylene oxide, and polypropylene oxide. Suitable polyelectrolytes are polyacids or polybases. Examples of polyacids are alkali salts of polyacrylic acid or comb-type polyacid polymers. Examples of polybases are polyvinylamines or polyethyleneamines. Suitable adjuvants are compounds that have little or even no pesticidal activity and that enhance the biological performance of compound I at the target. Examples include surfactants, mineral or vegetable oils, and other auxiliaries. Further examples are listed in Knowles, Adjuvants and Additives, Agrow Reports DS256, T&F Informa UK, 2006, Chapter 5. Suitable thickeners include polysaccharides (e.g., xanthan gum, carboxymethylcellulose), inorganic clays (organically modified or unmodified), polycarboxylates, and silicates. Suitable bactericides are bronopol and isothiazolinone derivatives, such as alkylisothiazolinones and benzisothiazolinones. Suitable antifreezes are ethylene glycol, propylene glycol, urea, and glycerin. Suitable antifoaming agents include silicones, long-chain alcohols, and fatty acid salts. Suitable colorants (e.g., in red, blue, or green) are pigments with low water solubility and water-soluble dyes. Examples include inorganic dyes (e.g., iron oxide, titanium oxide, iron hexacyanoferrate) and organic dyes (e.g., alizarin, azo, and phthalocyanine dyes). Suitable stickiness enhancers or binders include polyvinyl acetates, polyvinyl alcohols, polyacrylates, biological or synthetic waxes, and cellulose ethers. In general, the agrochemical compositions comprise from 0.01 to 95%, preferably from 0.1 to 90%, and in particular from 0.5 to 75% by weight of active substance. The active substances are used at a purity of 90% to 100%, preferably from 95% to 100% (according to the NMR spectrum). Seed treatment solutions (LS), suspensions (SE), flowable concentrates (FS), dry treatment powders (DS), water-dispersible suspension treatment powders (WS), water-soluble powders (SS), emulsions (ES), emulsifiable concentrates (EC), and gels (GF) are frequently used for treating plant propagation materials, particularly seeds. These compositions, after dilution two to ten times, yield active substance concentrations of 0.01 to 60% by weight, preferably 0.1 to 40% by weight, in ready-to-use preparations. Application can be carried out before or during sowing. Methods for applying compound I and its compositions to plant propagation material, especially seeds, include coating, swabbing, pelleting, dusting, soaking, and furrow application.Preferably, compound I or its compositions, respectively, are applied to the plant propagation material by a method that does not induce germination, for example, by coating, pelleting, seed coating and seed dusting. When used for plant protection, the amount of active substances applied varies, according to the type of effect desired, from 0.001 to 2 kg per ha, preferably from 0.005 to 2 kg per ha, more preferably from 0.05 to 0.9 kg per ha and, in particular, from 0.1 to 0.75 kg hQA7nn / l 7P7 / E / YILI per ha. For the treatment of plant propagation materials, such as seeds, for example, by dusting, coating, or soaking, the quantities of active substance generally required are 0.1 to 1000 g, preferably 1 to 1000 g, more preferably 1 to 1000 g, and most preferably 5 to 100 g per 100 kilograms of plant propagation material (preferably seeds). In some cases, the treatment quantity for seeds may be up to 100 g per 100 kilograms of seeds, or even exceed the weight of the seeds. When used for the protection of stored materials or products, the amount of active substance applied depends on the type of application area and the desired effect. The amounts typically applied for material protection are 0.001 g / 2 kg, preferably 0.005 g / 1 kg, of active substance per cubic meter of treated material. Various types of oils, wetting agents, adjuvants, fertilizers or micronutrients, and other pesticides (e.g., herbicides, insecticides, fungicides, growth regulators, protectants) can be added to the active substances or compositions comprising them, either as premixes or, if appropriate, only immediately before use (tank mixing). These agents can be mixed with the compositions according to the invention in a weight ratio of 1:100 to 100:1, preferably 1:10 to 10:1. In general, the user applies the composition according to the invention, using a pre-dosing device, a backpack sprayer, a spray tank, a spray aircraft, or an irrigation system. The agrochemical composition is often composed of water, a buffer, and / or other auxiliaries at the desired application concentration, resulting in a ready-to-use agrochemical composition or spray liquor. Typically, 20 to 2000 liters, preferably 50 to 400 liters, of the ready-to-use spray liquor are applied per hectare of usable agricultural area. According to one embodiment, the user can mix the individual components of the composition according to the invention, such as parts of a kit or parts of a binary or ternary mixture, in a spray tank, and other auxiliaries can be added, if appropriate. In another embodiment, the user can mix the individual components of the composition according to the invention or the partially mixed components beforehand, for example, components comprising active compound I and / or active compounds II (and, optionally, active compounds III), in a spray tank, and other auxiliaries and additives can be added, if appropriate. In another embodiment, the individual components of the composition according to the invention or the partially premixed components, for example, components comprising active compound I and / or active compounds II (and, optionally, active compounds III), can be applied together (for example, after mixing in the tank) or sequentially. Applications Compound I and one or more compounds II (and, optionally, compounds II) can be applied simultaneously, i.e., jointly or separately, or successively, i.e., immediately after one another, thereby creating the in-situ mixture at the desired location, for example, in the plant; in general, the sequence, in the case of separate application, has no effect on the outcome of the control measurements. The mixtures of the present invention are used as such or in the form of compositions for treating insects, fungi, or plants, plant propagation materials such as seeds, soil, surfaces, materials, or rooms that are to be protected against insect attack, with an effective pesticide quantity of the active compounds. Application can be carried out before and after insects infest the plants or plant propagation materials such as seeds, soil, surfaces, materials, or rooms. The present invention also includes a method for combating harmful animal and fungal pests, comprising bringing the fungi and / or animal pests, their habitat, breeding site, food supply, cultivated plants, seeds, soil, area, material or environment where the animal pests grow or can grow, or the materials, plants, seeds, soils, surfaces or spaces that are to be protected against attack or infestation by animals, into contact with an effective pesticide quantity of a mixture according to the present invention.The plants that can be treated with the mixtures of the invention include all genetically modified or transgenic plants, for example, crops that tolerate the action of herbicides, fungicides or insecticides due to breeding methods, including genetic engineering methods, or plants that have modified characteristics compared to existing plants, which can be generated, for example, by traditional breeding methods and / or the generation of mutants, or by recombination procedures. Some of the mixtures of the invention have systemic action and, therefore, can be used to protect plant shoots against foliar pests and also for the treatment of seeds and roots against pests that live in the soil. The mixtures of compounds I and II, or their corresponding formulations, are applied by treating harmful fungi and animal pests, their habitat, or the plants, seeds, soils, areas, materials, or spaces to be kept free of them, with an effective pesticide quantity of the mixture or, in the case of separate application, of compounds I and II. Application can be made before or after infection by harmful fungi and / or animal pests. Generally, compound I and one or more compounds II are applied in a weight ratio of 500:1 to 1:100, preferably 20:1 to 1:50, in particular 5:1 to 1:20. Depending on the desired effect, the application rates of the mixtures according to the invention are from 5 g / ha to 2000 g / ha, preferably from 50 to 1500 g / ha, in particular from 50 to 750 g / ha. Generally, synergistically effective amount means that one active compound I and one or more active compounds II are applied in a weight ratio of 500:1 to 1:100, preferably 20:1 to 1:50, in particular 5:1 to 1:20. Depending on the nature of the compounds, the range of the weight ratio employed between compound I and compounds II may start from 100:1 to 1:100, preferably 20:1 to 1:20, in particular 10:1 to 1:10. Additionally, if desired, additional active compounds, such as Compound III, are mixed in a ratio of 20:1 to 1:20 with respect to Compound I. The mixtures according to the invention are effective by contact and ingestion. According to a preferred embodiment of the invention, the mixtures according to the present invention are used by application to the soil. Soil application is particularly convenient for use against ants, termites, crickets, or cockroaches. According to another preferred embodiment of the invention, for use against non-crop pests such as ants, termites, wasps, flies, mosquitoes, crickets, locusts, or cockroaches, the mixtures according to the invention are prepared in a bait preparation. The bait can be a liquid, solid or semi-solid preparation (for example, a gel). Another aspect of the present invention is that when preparing the mixtures, it is preferable to use the pure active compounds I and II, to which other active compounds can be added, for example, against harmful fungi, or that have herbicidal activity, growth-regulating agents or fertilizers. The compositions of the present invention also contain other active ingredients not listed above. For example, fungicides, herbicides, fertilizers such as ammonium nitrate, urea, potash, and superphosphate, phytotoxic agents, plant growth regulators, and protectants. These additional ingredients can be used sequentially or in combination with the compositions described above, and can be added, if appropriate, just before use (tank mixing). For example, plants can be sprayed with a composition of the present invention before or after treatment with other active ingredients. The mixtures according to the invention can be applied at all developmental stages, such as egg, larva, pupa, and adult. Pests can be controlled by contact of the target pest, its food supply, habitat, breeding site, or locus with an effective pesticide quantity of the mixtures of the invention or of the hQA7nn / l 7P7 / B / YILI compositions comprising the mixtures. Locus means a plant, a seed, a soil, an area, a material, or an environment in which a pest develops or can develop. In general, the effective amount as a pesticide means the quantity of the mixtures of the invention or of the compositions comprising the mixtures, necessary to achieve a substantial effect on the growth, including effects of necrosis, death, retardation, prevention and elimination, destruction, or reduction of the occurrence and activity of the target organism. The effective amount as a pesticide may vary depending on the different mixtures and / or compositions used in the invention. An effective amount as a pesticide of the mixtures and / or compositions will also vary according to the prevailing conditions, such as the desired pesticide effect and duration, the climate, the target species, the locus, the mode of application, and the like. The mixtures of the invention or compositions of these mixtures can also be used to protect plants from attack or infestation by insects, mites or nematodes, comprising putting a plant, or the soil or water in which the plant grows, into contact with the mixture. The mixtures of the invention are effective by contact (through soil, glass, wall, mosquito net, carpet, plant parts or animal parts) and by ingestion (bait or plant part) and by trophallaxis and transfer. The preferred application methods are in bodies of water, through soil, cracks and crevices, pastures, compost heaps, hQA7nn / l 7P7 / B / YILI sewers, in water, soil, wall, or by perimeter spray and bait application. The mixtures of the invention and the compositions comprising them can be used to protect wooden materials, such as trees, fences, sleepers, etc., and constructions, such as houses, outdoor latrines, factories, and also building materials, furniture, leather, fibers, vinyl articles, wiring and electrical wires, etc. In the case of soil treatment or application to places or nests where pests live, the amount of active ingredients varies from 0.0001 to 500 g per 100 m2, preferably from 0.001 to 20 g per 100 m2. Typical application rates for material protection are, for example, 0.01 g 1000 g of active compounds per m2 of treated material, preferably 0.1 g 50 g per m2. For use in spray compositions, the content of the mixture of active ingredients is from 0.001 to 80% by weight, preferably from 0.01 to 50% by weight and, most preferably, from 0.01 to 15% by weight. For use in the treatment of crop plants, the application rate of the mixture of active ingredients of this invention may vary from 0.1 g to 4000 g per hectare, preferably from 25 g to 600 g per hectare, with greater preference from 50 g to 500 g per hectare. The treatment method according to the invention can also be used in the field of protecting stored products or crops against attack by animal pests, fungi, and microorganisms. According to the present invention, the term "stored products" refers to natural substances of plant or animal origin and their processed forms, taken from the natural life cycle and for which prolonged protection is desired. Stored products of cultivated plants, such as plants or parts thereof, for example, stems, leaves, tubers, seeds, fruits, or grains, can be protected in their freshly grown state or in a processed form, such as previously dried, moistened, shredded, ground, pressed, or roasted, a process also known as post-harvest treatment.The definition of stored products also includes wood, whether in the form of raw timber, such as lumber for construction, high-voltage towers, and barriers, or in the form of finished articles, such as furniture or wooden objects. Stored products of animal origin include hides, skins, hair, and the like. Combinations according to the present invention can prevent undesirable effects, such as deterioration, discoloration, or mold. Preferably, the term "stored products" refers to natural substances of plant origin and their processed forms, most preferably fruits and their processed forms, such as pome fruits, stone fruits, soft fruits, and citrus fruits, and their processed forms. In the context of the present invention, the term plant refers to a whole plant, a part of a plant, or plant propagation material. hQA7nn / l 7Π7 / Β / YΙΛΙ 100 The mixtures of the present invention and the compositions comprising it are particularly important for the control of multiple insects in various cultivated plants. The plants that can be treated with the mixtures of the invention include all genetically modified or transgenic plants, for example, crops that tolerate the action of herbicides, fungicides or insecticides due to breeding methods, including genetic engineering methods, or plants that have modified characteristics compared to existing plants, which can be generated, for example, by traditional breeding methods and / or the generation of mutants, or by recombination procedures. The term "plant propagation material" refers to all generative parts of a plant, such as seeds and vegetative plant material, including cuttings and tubers (e.g., potatoes), that can be used for plant multiplication. This includes seeds, roots, fruits, tubers, bulbs, rhizomes, shoots, buds, and other plant parts. It also includes seedlings and young plants that will be transplanted after germination or emergence from the soil. These young plants may also be protected before transplanting by partial or complete treatment, such as immersion or watering. The term cultivated plants includes plants that have been modified by breeding, mutagenesis, or genetic engineering. Genetically modified plants are plants whose genetic material hQA7nn / l 7Π7 / Β / Y Gene 101 was modified using recombinant DNA techniques that, under natural circumstances, cannot be obtained through cross-pollination, mutation, or natural recombination. Generally, one or more genes are integrated into the genetic material of a genetically modified plant to improve certain plant properties. The expression cultivated plants also includes plants that have become tolerant to applications of specific classes of herbicides, such as hydroxyphenylpyruvate dioxygenase (HPPD) inhibitors; Acetolactate synthase (ALS) inhibitors, such as sulfonylureas (see, for example, US 6.222.100, WO 01 / 82685, WO 00 / 26390, WO 97 / 41218, WO 98 / 02526, WO 98 / 02527, WO 04 / 106529, WO 05 / 20673, WO 03 / 14357, WO 03 / 13225, WO 03 / 14356, WO 04 / 16073) or imidazolinones (see, for example, US 6.222.100, WO 01 / 82685, WO 00 / 26390, WO 97 / 41218, WO 98 / 02526, WO 98 / 02527, WO 04 / 106529, WO 05 / 20673, WO 03 / 14357, WO 03 / 13225, WO 03 / 14356, WO 04 / 16073); enolpyruvylshikimate-3-phosphate (EPSPS) inhibitors, such as glyphosate (see, for example, WO 92 / 00377); glutamine synthetase (GS) inhibitors, such as glufosinate (see, for example, EP-A-0242236, EP-A-242246) or oxynyl herbicides (see, for example, US 5.559).024) as a result of conventional breeding methods or genetic engineering. Several cultivated plants were made herbicide-tolerant by conventional breeding methods (mutagenesis), for example, Clearfield® summer rapeseed (Canola) tolerant to imidazolinones, for example, imazamox. Genetic engineering methods were used to make cultivated plants, hQA7nn / l 7P7 / B / YILI. 102 such as soybeans, cotton, corn, beets, and rapeseed, became tolerant to herbicides such as glyphosate and glufosinate, some of which are available commercially under the trade names RoundupReady® (glyphosate) and LibertyLink® (glufosinate). The expression cultivated plants also includes plants that are, thanks to the use of recombinant DNA techniques, capable of synthesizing one or more insecticidal proteins, especially those known from the bacterial genus Bacillus, in particular Bacillus thuringiensis, such as delta-endotoxins, for example, CrylA(b), CrylA(c), CrylF, CrylF(a2), CryllA(b), CrylllA, CrylllB(b1) or Cry9c; vegetative insecticidal proteins (VIPs), for example, VIP1, VIP2, VIP3 or VIP3A; insecticidal proteins from nematodes colonizing bacteria, for example, Photorhabdus spp. or Xenorhabdus spp.; toxins produced by animals, such as scorpion toxins, arachnid toxins, wasp toxins, or other insect-specific neurotoxins; toxins produced by fungi, such as Streptomycetes toxins, plant lectins, such as pea or barley lectins; agglutinins; proteinase inhibitors, such as trypsin inhibitors, serine protease inhibitors, patatin, cystatin, or papain inhibitors; ribosome-inactivating proteins (RIPs), such as ricin, maize RIP, abrin, lufin, saporin, or bryodin; steroid metabolism enzymes, such as 3-hydroxysteroid oxidase, ecdysteroid-IDP-glycosyltransferase, cholesterol oxidases, ecdysone inhibitors, or HMG-CoA reductase; ion channel blockers, such as sodium or calcium channel blockers; hQRjnn / l 7Π7 / Β / Υ esterase. 103 juvenile hormone; diuretic hormone receptors (helicokinin receptors); stilbene synthase, bibenzyl synthase, chitinases, or glucanases. In the context of the present invention, these insecticidal proteins or toxins are to be expressly interpreted also as pretoxins, hybrid proteins, truncated proteins, or otherwise modified proteins. Hybrid proteins are characterized by a novel combination of protein domains (see, for example, WO 02 / 015701). Further examples of such toxins or genetically modified plants capable of synthesizing such toxins are described, for example, in EP-A 374 753, WO 93 / 007278, WO 95 / 34656, EP-A 427 529, EP-A 451 878, WO 03 / 018810, and WO 03 / 052073. In general, the methods for producing these genetically modified plants are known to the average person in the trade and are described, for example, in the publications mentioned above.These insecticidal proteins contained in genetically modified plants give the plants that produce these proteins tolerance to harmful pests from all taxonomic groups of insects, especially beetles (Coleoptera), two-winged insects (Diptera) and butterflies (Lepidoptera). The term "cultivated plants" also includes plants that, through the use of recombinant DNA techniques, are capable of synthesizing one or more proteins to increase their resistance or tolerance to bacterial, viral, or fungal pathogens. Examples of such proteins include pathogenesis-related proteins (PR proteins, see, for example, EP-A 0 392 225) and plant disease-resistant genes (for example, cultivars hQRjnn / l 7P7 / B / Y). 104 potato varieties expressing resistant genes that act against Phytophthora infestans (derived from the Mexican wild potato Solanum bulbocastanum) or T4-lysozyme (for example, potato cultivars capable of synthesizing these proteins with greater resistance to bacteria, such as Erwinia amylvora). In general, the methods for producing these genetically modified plants are known to the average person and are described, for example, in the publications mentioned above. The expression cultivated plants also includes plants that are, thanks to the use of recombinant DNA techniques, capable of synthesizing one or more proteins to increase productivity (e.g., biomass production, grain yield, starch content, oil content or protein content), tolerance to drought, salinity or other environmental factors that limit growth, or tolerance to pests and fungal, bacterial or viral pathogens of such plants. The term cultivated plants also includes plants that contain, thanks to the use of recombinant DNA techniques, a modified amount of content substances or new content substances, specifically to improve human or animal nutrition, for example, oilseed crops that produce long-chain omega-3 fatty acids that improve health or unsaturated omega-9 fatty acids (for example, Nexera® rapeseed). The expression cultivated plants also includes plants that contain, thanks to the use of recombinant DNA techniques, an hQA7nn / l 7Π7 / Β / Y 105 modified quantity of content substances or new content substances, specifically to improve the production of raw materials, for example, potatoes that produce a higher quantity of amylopectin (for example, Amflora® potato). Some of the mixtures of the invention have systemic action and, therefore, can be used to protect plant shoots against foliar pests and also for the treatment of seeds and roots against soil-dwelling pests. Seed treatment Therefore, the mixtures according to the present invention are suitable for seed treatment, in order to protect the seed against insect pests, in particular against soil-dwelling insect pests, and the resulting roots and shoots of the plant against soil-dwelling and foliar insect pests. Protection of the roots and the resulting shoots of the plant is preferred. It is of greater preference to protect the resulting plant shoots against incisor and sucking insects. Therefore, the present invention comprises a method for protecting seeds from insects, in particular soil-dwelling insects, and for protecting the roots and shoots of the seedling from insects, in particular foliar and soil-dwelling insects, wherein said method comprises contacting the seeds before sowing and / or after pre-germination with mixtures according to hQA7nn / l 7P7 / B / Y 106 with the present invention. In particular, a method is preferred for protecting the roots and shoots of the plant, more preferably a method for protecting the shoots of the plants against incisor-sucking insects, and most preferably a method for protecting the shoots of the plants against aphids. The term 'seed' includes all types of seeds and plant propagules, including, inter alia, true seeds, parts of seeds, suckers, corms, bulbs, fruits, tubers, grains, cuttings, cut shoots and the like, and in a preferred embodiment, means true seeds. The term seed treatment comprises all suitable techniques known in the state of the art for the treatment of seeds, such as disinfection, coating, dusting, soaking and pelleting of seeds. The present invention also includes seeds coated with or containing the active compounds. In general, the terms coated and / or containing mean that the active ingredients are primarily on the surface of the propagation product at the time of application, although a greater or lesser portion of the ingredient may penetrate the propagation product, depending on the application method. When these propagation products are (re)planted, they may absorb the active ingredient. Suitable seeds include cereal seeds, root crops, oil crops, vegetables, spices, ornamentals, for example, hQRjnn / i ζηζ / E / γ 107 durum wheat seed and other types of wheat, barley, oats, rye, corn (forage corn and sugar corn / sweet and field wheat), soybeans, oilseed crops, cruciferous plants, cotton, sunflower, banana, rice, oilseed rape, turnip, sugar beet, fodder beet, eggplant, potato, grass, lawn, turf, forage grass, tomato, leek, squash / pumpkin, cabbage, iceberg lettuce, pepper, cucumber, melon, Brassica species, cantaloupe, bean, pea, garlic, onion, carrot, tuberous plants such as potato, sugar cane, tobacco, vine, petunia, geranium / pelargonium, pansies and impatiens. Furthermore, the mixtures according to the invention can also be used for the treatment of plant seeds, which are tolerant to the action of herbicides, fungicides or insecticides due to breeding methods, including genetic engineering methods. For example, active mixtures can be used for the treatment of plant seeds, which are resistant to herbicides of the group consisting of sulfonylureas, imidazolinones, glufosinate-ammonium or glyphosate-isopropylammonium and analogous active substances (see, for example, EP-A-0242236, EP-A-242246) (WO 92 / 00377) (EP-A-0257993, U.S. Patent No. 5,013,659) ) or in transgenic crop plants, for example, cotton, which are capable of producing Bacillus thuringiensis toxins (Bt toxins) that make the plants resistant to certain pests (EP-A-01 42924, EP-A-01 93259), Furthermore, the mixtures according to the present invention can be used for the treatment of plant seeds, which have hQA7nn / i ζηζ / E / γ 108 modified characteristics compared to existing plants, which can be generated, for example, by traditional breeding methods and / or the generation of mutants, or by recombinant procedures). For example, several cases of recombinant modifications of crop plants have been described in order to modify the starch synthesized in the plants (for example, WO 92 / 1 1376, WO 92 / 14827, WO 91 / 19806) or of transgenic crop plants that have a modified fatty acid composition (WO 91 / 13972). The application of the seed treatment to the mixtures is carried out by spraying or dusting the seeds before sowing the plants and before the plants emerge. In seed treatment, the corresponding formulations are applied by treating the seeds with an effective quantity of the mixture according to the present invention. Herein, the application rates of the active compounds generally range from 0.1 to 10 kg per 100 kg of seeds, preferably from 1 to 5 kg per 100 kg of seeds, and particularly from 1 to 2.5 kg per 100 kg of seeds. For specific crops, such as lettuce, the rate may be higher. Furthermore, in some other cases, the quantity for seed treatment may be up to 100 kilograms of the active compounds per 100 kilograms of seeds or may even exceed the weight of the seeds. Compositions that are especially useful for seed treatment include, for example: A Soluble Concentrates (SL, LS) hQA7nn / i ζηζ / E / γ 109 D Emulsions (EW, EO, ES) E Suspensions (SC, OD, FS) F Water-dispersible granules and water-soluble granules (WG, SG) G Water-dispersible powders and water-soluble powders (WP, SP, WS) H Gel formulations (GF) I Powders that can be converted into powders (DP, DS) Conventional seed treatment formulations include, for example, fluid concentrates (FS), solutions (LS), dry treatment powders (DS), water-dispersible suspension powders (WS), water-soluble powders (SS), emulsions (ES and EC), and gel formulations (GF). These formulations can be applied to the seed diluted or undiluted. Application to the seeds is carried out before sowing, either directly onto the seeds or after pre-germination. In a preferred embodiment, an FS formulation is used for seed treatment. Typically, an FS formulation may comprise 1–800 g / L of active ingredients, 1–200 g / L of surfactant, 0–200 g / L of antifreeze agent, 0–400 g / L of binder, 0–200 g / L of a pigment, and up to 1 L of a solvent, preferably water. The preferred FS formulations of the Formula I compounds for seed treatment comprise 0.1 to 80 wt% (1 to 800 g / l) of the active ingredients, 0.1 to 20 wt% (1 to 200 g / l) of at least one surfactant, for example, 0.05 to 5 wt% of a wetting agent, and 0.5 to 15 wt% of an agent hQB7nn / i znz / E / YiAi 110 dispersant, up to 20% by weight, for example, 5 to 20% of an antifreeze agent, 0 to 15% by weight, for example, 1 to 15% by weight of a pigment and / or dye, 0 to 40% by weight, for example, 1 to 40% by weight of a binder (tack / adhesion agent), optionally up to 5% by weight, for example, 0.1 to 5% by weight of a thickener, optionally 0.1 to 2% of an antifoaming agent and, optionally, a preservative such as a biocide, antioxidant or the like, for example, in an amount of 0.01 to 1% by weight and a filler / vehicle agent up to 100% by weight. Seed treatment formulations may also contain binders and, optionally, colorants. Binders can be added to improve the adhesion of active materials to seeds after treatment. Suitable binders include EO / PO block copolymer surfactants, as well as polyvinyl alcohols, polyvinyl pyrrolidones, polyacrylates, polymethacrylates, polybutenes, polyisobutylenes, polystyrene, polyethyleneamines, polyethyleneamides, polyethyleneimines (Lupasol®, Polymin®), polyethers, polyurethanes, polyvinyl acetate, tyloses, and copolymers derived from these polymers. Optionally, colorants can also be included in the formulation. Suitable colorants or dyes for seed treatment formulations include: Rhodamine B, Pigment Red 112, Solvent Red 1, 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, and Pigment hQA7nn / l 7P7 / B / YILI 111 red 48:1, red pigment 57:1, red pigment 53:1, orange pigment 43, orange pigment 34, orange pigment 5, green pigment 36, green pigment 7, white pigment 6, brown pigment 25, basic violet 10, basic violet 49, acid red 51, acid red 52, acid red 14, acid blue 9, acid yellow 23, basic red 10, basic red 108. The invention also relates to mixtures comprising seeds, according to the present invention. In general, the amount of compound I or its salt useful in agriculture varies from 0.1 g to 10 kg per 100 kg of seeds, preferably from 1 g to 5 kg per 100 kg of seeds, and in particular, from 1 g to 1000 g per 100 kg of seeds. Examples B. Biology Synergy can be described as an interaction in which the combined effect of two or more compounds is greater than the sum of the individual effects of each compound. The presence of a synergistic effect, in terms of percentage control, between two mixture components (X and Y) can be calculated using the Colby equation (Colby, SR, 1967, Calculating Synergistic and Antagonistic Responses in Herbicide Combinations, Weeds, 15, 20-22): E = X + Y - 100 When the effect of the observed combined control is greater than the effect of the expected combined control (E), then the combined effect is synergistic. The analysis of synergy or antagonism between the bQRynn / i ζπζ / β / υιλι was determined 112 mixtures or compositions using the Colby equation. B.1 Pesticide action against fungi Microassay for the evaluation of fungicidal activity The active compounds were formulated separately as a stock solution that had a concentration of 10,000 ppm in dimethyl sulfoxide. B.1.1. Activity against the rice fungus Pyricularia oryzae The stock solutions were mixed according to the stated ratio, pipetted onto a microtiter plate (MTP), and diluted with water to the stated concentrations. A suspension of Pyricularia oryzae spores in an aqueous biomalt or yeast-bactopeptonaglycerin solution was then added. The plates were placed in a steam-saturated chamber at 18 °C. Using an absorption photometer, the MTP concentrations were measured at 405 nm, 7 days post-inoculation. The results are shown in Table B.1.1 below. hQRjnnn znz / E / YiAi Table B.1.1. : Pyricularia oryzae Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) carboxamide compound of the 16 - 4 4 - 15 113 Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) Formula I 1 - 12 0.063 - 2 Epoxiconazole 0.25 0.063 28 1 carboxamide compound of Formula I 16 64:1 100 31 69 Epoxiconazole 0.25 carboxamide compound of Formula I Epoxiconazole 4 0.063 63:1 100 15 85 carboxamide compound of Formula I Epoxiconazole 4 0.25 16:1 100 39 61 carboxamide compound of Formula I 1 16:1 100 13 87 hQA7nn / l 7Π7 / Β / YΙΛΙ 114 Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) Epoxiconazole 0.063 B.1.2. Activity against leaf spots of wheat caused by Septoria tritici The stock solutions were mixed according to the stated ratio, pipetted onto a microtiter plate (MTP), and diluted with water to the stated concentrations. A suspension of Septoria tritici spores in an aqueous solution of biomalt or yeast-bactopeptonaglycerin was then added. The plates were placed in a steam-saturated chamber at 18 °C. Using an absorption photometer, the MTP concentrations were measured at 405 nm, 7 days post-inoculation. The results are shown in Table B.1.2 below. 115 Table B.1.2.: Septoria tritici Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) Carboxamide compound of Formula I 63 - 11 Epoxiconazole 0.016 - 7 Metalaxyl 4 1 - 5 5 Triticonazole 0.063 - 5 Carboxamide compound of Formula I 63 4000:1 49 18 31 Epoxiconazole 0.016 Carboxamide compound of Formula 63 16:1 45 15 30 hQRjnnn znz / E / YiAi Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) I Metalaxyl 4 carboxamide compound of Formula I Metalaxyl 63 1 63:1 40 15 25 carboxamide compound of Formula IT riticonazole 63 0.063 1000:1 42 16 26 B.1.3. Activity against early blight caused by Alternaria solani The stock solutions were mixed according to the stated ratio, pipetted onto a microtiter plate (MTP), and diluted with water to the stated concentrations. A suspension of Alternaria solani spores in an aqueous biomalt or yeast-bactopeptonaglycerin solution was then added. The plates were placed in a vapor-saturated chamber of hQA7nn / l 7P7 / B / YILI 117 C. Co days B.1.3 water at a temperature of 18° MTPs were measured at 405 nm, 7 results are indicated in Table n after inoculation. Table B.1.3.: Alternaria sotaní Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) compound of 63 - 0 carboxamide 16 - 0 of Formula 4 - 0 I 1 - 0 Pyraclostrobin 0.063 0.016 12 0 Triticonazole 1 - 23 0.25 - 0 carboxamide compound of Formula I 16 254:1 36 12 24 Pyraclostrobin 0.063 compound of 63 1000:1 40 12 28 118 Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) Formula I carboxamide Pyraclostrobin 0.063 Formula I carboxamide compound Pyraclostrobin 63 0.016 4000:1 24 0 24 Formula IT carboxamide compound Riticonazole 63 1 63:1 43 23 20 Formula IT carboxamide compound Riticonazole 16 0.25 64:1 32 0 32 hQA7nn / l 7Π7 / Β / YΙΛΙ 119 Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) Carboxamide compound of Formula IT riticonazole 4 0.25 16:1 20 0 20 Carboxamide compound of Formula IT riticonazole 4 1 4:1 52 23 29 Carboxamide compound of Formula I 1 4:1 34 0 34 T riticonazole 0.25 B.1.4. Activity against leaf spots in wheat caused by Leptosphaeria nodorum The stock solutions were mixed according to the indicated ratio, and placed with a pipette onto an hQA7nn / l 7Π7 / Β / YILI plate 120 µmTs (MTPs) were added and diluted with water to the indicated concentrations. Then, a suspension of Leptosphaeria nodorum spores in an aqueous solution of biomalt or yeast-bactopeptone-glycerin was added. The plates were placed in a steam-saturated chamber at 18 °C. Using an absorption photometer, MTPs were measured at 405 nm, 7 days after inoculation. The results are shown in Table B.1.4 below. hQRjnn / l 7Π7 / Β / Y Table B.1.4.: Leptosphaeria nodorum Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) Formula I carboxamide compound 4 - 1 Pyraclostrobin 0.25 - 72 Formula I carboxamide compound Pyraclostrobin 4 0.25 16:1 100 72 28 121 B.1.5. Activity against Microdochium nivale The stock solutions were mixed according to the stated ratio, pipetted onto a microtiter plate (MTP), and diluted with water to the stated concentrations. A suspension of Microdochium nivale spores in an aqueous biomalt or yeast-bactopeptone-glycerin solution was then added. The plates were placed in a steam-saturated chamber at 18 °C. Using an absorption photometer, the MTP concentrations were measured at 405 nm, 7 days post-inoculation. The results are shown in Table B.1.5 below. Table B.1.5: Microdochium nivale hQRjnn / i znz / E / YiAi Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) Compound of 63 - 4 carboxamide 16 - 15 of Formula I 4 - 13 Pyraclostrobin 0.016 - 46 0.063 - 0 Fluxapyroxad 0.004 - 0 122 Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) Epoxiconazole 0.016 0.004 29 8 Carboxamide compound of Formula I Pyraclostrobin 4 0.016 250:1 79 53 26 Carboxamide compound of Formula I Pyraclostrobin 16 0.016 1000:1 74 54 20 Carboxamide compound of Formula I Pyraclostrobin 63 0.016 4000:1 93 48 45 Carboxamide compound 63 1000:1 35 4 31 hQA7nn / l 7Π7 / Β / YΙΛΙ 123 Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) of Formula I Fluxapyroxad 0.063 carboxamide compound of Formula I Fluxapyroxad 63 0.004 16000:1 25 4 21 carboxamide compound of Formula I Epoxiconazole 4 0.016 250:1 63 38 25 carboxamide compound of Formula I 63 4000:1 99 31 68 Epoxiconazole 0.016 compound of 16 4000:1 99 21 78 124 Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) Formula I carboxamide Epoxiconazole 0.004 B.1.6. Activity against Flhizoctonia solani The stock solutions were mixed according to the stated ratio, pipetted onto a microtiter plate (MTP), and diluted with water to the stated concentrations. A suspension of *Flhizoctonia solani* spores in an aqueous solution of biomalt or yeast-bactopeptonaglycerin was then added. The plates were placed in a steam-saturated chamber at 18 °C. Using an absorption photometer, the MTP concentrations were measured at 405 nm, 7 days post-inoculation. The results are shown in Table B.1.6 below. Table B.1.6.: Flhizoctonia solani 125 Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) Carboxamide compound 16 - 0 4 - 0 of Formula I 1 - 0 0.016 - 24 Epoxiconazole 0.004 - 0 0.001 - 0 Triticonazole 0.25 - 41 Carboxamide compound of Formula I 4 250:1 55 24 31 Epoxiconazole 0.016 Carboxamide compound of Formula I 63 4000:1 96 31 65 Epoxiconazole 0.016 Carboxamide compound of Formula I 16 4000:1 75 0 75 Epoxiconazole 0.004 hQAznn / i ζηζ / E / γ 126 Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) Formula I carboxamide compound Epoxiconazole 4 0.001 4000:1 20 0 20 Formula I carboxamide compound Epoxiconazole 1 0.016 63:1 44 24 20 Formula IT carboxamide compound Riticonazole 16 0.25 64:1 67 41 26 Formula IT carboxamide compound Riticonazole 4 0.25 16:1 67 41 26 Formula I carboxamide compound 1 4:1 69 41 28 hQA7nn / i ζηζ / E / γ 127 Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) Triticonazole 0.25 B.1.7. Activity against Pyrenophora teres The stock solutions were mixed according to the stated ratio, pipetted onto a microtiter plate (MTP), and diluted with water to the stated concentrations. A suspension of Pyrenophora teres spores in an aqueous solution of biomalt or yeast-bactopeptonaglycerin was then added. The plates were placed in a steam-saturated chamber at 18 °C. Using an absorption photometer, the MTP concentrations were measured at 405 nm, 7 days post-inoculation. The results are shown in Table B.1.7 below. 128 hQA7nn / l 7Π7 / E / YILI Table B.1.7.: Pyrenophora teres 5 Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) Compound 63 - 20 carboxamide 16 - 0 of Formula 10 I 4 - 0 Pyraclostrobin 0.016 - 34 Epoxiconazole 0.016 - 0 Compound 15 carboxamide of Formula I 4 250:1 61 34 27 Pyraclostrobin 0.016 Compound 20 carboxamide of Formula I 16 1000:1 67 34 33 Pyraclostrobin 0.016 Compound 63 4000:1 73 20 53 129 Active compound / active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) Formula I carboxamide Epoxiconazole 0.016 hQA7nn / i ζηζ / E / γ The measured parameters were compared with the growth of the active compound-free control variant (100%) and with the fungus-free and active compound-free blank value to determine the relative % growth of the pathogens in the respective active compounds. These percentages were converted into efficiencies. As mentioned above, the predicted efficacies of the active compound mixtures were determined using the Colby formula [RS Colby, “Calculating synergistic and antagonistic responses of herbicide combinations, Weeds 15, 20-22 (1967)] and compared with the observed efficacies. Furthermore, the following additional test systems can be used to demonstrate and evaluate the fungicidal action of compounds, mixtures, or compositions of the present invention on specific fungi. However, the protection afforded by the fungicidal control obtained through the compounds, mixtures, or compositions 130 is not limited to these fungi. In some cases, combinations of a compound of the present invention with other fungicidal compounds or agents have been found to have synergistic effects against certain important fungi. Unless otherwise specified and as described above, the active substances were formulated separately as a stock solution in dimethyl sulfoxide (DMSO) at a concentration of 10,000 ppm. The measured parameters were compared with the growth of the active compound-free control variant (100%) and with the fungus-free and active compound-free blank to determine the relative growth percentage of the pathogens on the respective active compounds. These percentages were then converted into efficacies. Example of fungicide test B.1.8: Activity against gray mold Botrytis cinerea in the microtiter plate test The stock solutions were mixed according to the desired ratio, pipetted onto a microtiter plate (MTP), and diluted with water to the specified concentrations. A suspension of Botrytis cinerea spores was added to an aqueous biomalt solution. The plates were placed in a steam-saturated chamber at 18 °C. Using an absorption photometer, the MTP concentrations were measured at 405 nm, 7 days post-inoculation. Example of fungicide test B.1.9: bQRynn / i znz / B / v 131 Activity against Septoria glycines in the microtiter plate test The stock solutions were mixed according to the desired ratio, pipetted onto a microtiter plate (MTP), and diluted with water to the specified concentrations. A suspension of Septoria glycines spores was added to an aqueous biomalt solution. The plates were placed in a steam-saturated chamber at 18 °C. Using an absorption photometer, the MTP concentrations were measured at 405 nm, 7 days post-inoculation. Example of fungicide test B.1.10: Activity against Colletotrichum truncatum in the microtiter plate test The stock solutions were mixed according to the ratio, pipetted onto a microtiter plate (MTP), and diluted with water to the indicated concentrations. A suspension of Colleotrichum truncatum spores was added to an aqueous biomalt solution. The plates were placed in a steam-saturated chamber at 18 °C. Using an absorption photometer, the MTP concentrations were measured at 405 nm, 7 days post-inoculation. Example of fungicide test B.1.11 Fungicidal control of brown spot caused by Cochliobolus miyabeanus (protectant) The leaves of rice seedlings grown in pots 132 plants were sprayed until thoroughly soaked with an aqueous suspension containing a specific concentration of active ingredients prepared from a stock solution. The plants were then allowed to air dry. The following day, the plants were inoculated with an aqueous suspension of Cochliobolus miyabeanus spores. The test plants were then immediately transferred to a humid chamber. After 6 days at a temperature of 22–24 °C and a relative humidity close to 100%, the extent of fungal attack on the leaves was visually assessed as a percentage of the diseased leaf area. Here too, the measured parameters from the fungicide trials were compared with the growth of the active compound-free control variant (100%) and with the fungi-free and active compound-free blank to determine the relative growth percentage of pathogens on the respective active compounds. These percentages were converted into efficacies. An efficacy of 0 means that the pathogen growth level corresponds to that of the untreated control; an efficacy of 100 means that the pathogens are not growing. B.2 Pesticide activity against animal pests The following tests can also demonstrate the control efficacy of the compounds, mixtures, or compositions of this invention against specific animal pests. However, the pest control protection obtained through the compounds, mixtures, or compositions is not limited to these species. In some cases, combinations of a compound of the present invention with other compounds or pest control agents hQA7nn / l 7P7 / B / Y were found to be effective. 133 invertebrate strains exhibit synergistic effects against certain important invertebrate pests. Example of insecticide test B.2.1: To evaluate, for example, the control of the pea aphid (Megoura viciae) by contact or with systemic means, the test unit consisted of 24-cavity microtiter plates containing bean leaf discs. The compounds or mixtures were formulated with a solution containing 75% water and 25% DIVISO. Different concentrations of the formulated mixtures or compounds were sprayed onto leaf discs at 2.5 µL using a custom-made microatomizer, with two replicates. For the experimental mixtures in these tests, identical volumes of both mixture pairs were mixed at the desired concentrations, respectively. After application, the leaf discs were air-dried, and 5–8 adult aphids were placed on the discs within the cavities of the microtiter plates. The aphids were then allowed to feed on the treated leaf discs, which were incubated at approximately 23 ± 1 °C and approximately 50 ± 5% RH (relative humidity) for 5 days. Aphid mortality and fecundity were visually assessed. Example of insecticide test B.2.2: To evaluate, for example, the control of the oat aphid (Rhopalosiphum padi) by contact or with systemic means, the hQA7nn / l 7Π7 / Β / Y The 134 test unit consisted of 96-cavity microtiter plates containing barley leaf discs. The compounds or mixtures were formulated with a solution containing 75% water and 25% DIVISO. Different concentrations of the formulated mixtures or compounds were sprayed onto leaf discs at 2.5 µL using a custom-made microatomizer, with two replicates. For the experimental mixtures in these tests, identical volumes of both mixture pairs were mixed at the desired concentrations, respectively. After application, the leaf discs were air-dried, and 5–8 adult aphids were placed on the discs within the cavities of the microtiter plates. The aphids were then allowed to feed on the treated leaf discs, which were incubated at approximately 25 ± 1 °C and around 80 ± 5% RH for 3–5 days. Aphid mortality and fecundity were visually assessed. Example of insecticide test B.2.3: To evaluate, for example, the control of the green peach aphid (Myzus persicae) with systemic media, the test unit consisted of 96-cavity microtiter plates, which contained a liquid artificial diet under an artificial membrane. The compounds or mixtures were formulated with a solution containing 75% water and 25% DMSO. Using a custom-made pipette, different concentrations of the mixtures or hQA7nn / i ζηζ / E / γ were placed into the solution. 135 compounds formulated in the diet of aphids, with two replicates. For the experimental mixtures in these tests, identical volumes of both mixture pairs were mixed at the desired concentrations, respectively. After application, 5–8 adult aphids were placed on the artificial membrane within the cavities of the microtiter plates. The aphids were then allowed to feed on the treated aphid diet and incubated at approximately 23 ± 1 °C and approximately 50 ± 5% RH for 3 days. Aphid mortality and fecundity were visually assessed. Example of insecticide test B.2.4: To evaluate, for example, the control of the boll weevil (Anthonomus grandis), the test unit consisted of 24-cavity microtiter plates containing an insect diet and 20-30 A. grandis eggs. The compounds or mixtures were formulated with a solution containing 75% water and 25% DMSO. Different concentrations of the formulated compounds or mixtures were sprayed onto the insect diet at 20 µL using a custom-made microatomizer, with two replicates. For the experimental mixtures in these tests, identical volumes of both mixture pairs were mixed at the desired concentrations, respectively. After application, the microtiter plates were incubated at around 23 ± 1 °C and around 50 ± 5% of hQB7nn / i ζηζ / E / γ 136 RH for 5 days. Egg and larval mortality was visually assessed. Example of insecticide test B.2.5: To evaluate, for example, the control of the Mediterranean fruit fly (Ceratitis capitata), the test unit consisted of 96-cavity microtiter plates, which contained an insect diet and 50-80 C. capitata eggs. The compounds or mixtures were formulated with a solution containing 75% water and 25% DMSO. Different concentrations of the formulated compounds or mixtures were sprayed onto the insect diet at 5 µL using a custom-made microatomizer, with two replicates. For the experimental mixtures in these tests, identical volumes of both mixture pairs were mixed at the desired concentrations, respectively. After application, the microtiter plates were incubated at approximately 28 ± 1 °C and approximately 80 ± 5% RH for 5 days. Egg and larval mortality was then visually assessed. Example of insecticide test B.2.6: To evaluate, for example, the control of the tobacco hornworm (Heliothis virescens), the test unit consisted of 96-cavity microtiter plates containing an insect diet and 15-25 H. virescens eggs. The compounds or mixtures were formulated with a solution that hQA7nn / l 7Π7 / Β / Y 137 contained 75% water and 25% DMSO. Regarding the insect diet, different concentrations of formulated compounds or mixtures were sprayed at 10 μL, using a custom-made microatomizer, with two replicates. For the experimental mixtures in these tests, identical volumes of both mixture pairs were mixed at the desired concentrations, respectively. After application, the microtiter plates were incubated at approximately 28 ± 1 °C and approximately 80 ± 5% RH for 5 days. Egg mortality and larval hQA7nn / l 7P7 / B / Y were visually assessed.

Claims

1. Agricultural mixtures comprising as active compounds 1) a carboxamide active compound as pesticide I of formula (I): hQA7nn / l 7P7 / B / YILI or a tautomer, enantiomer, diastereomer or salt thereof, and 2) at least one fungicidal active compound II selected from complex II inhibitors (e.g., carboxamides): benodanil, benzovindiflupyr, bixaphene, boscalid, carboxin, fenfuram, fluopyram, flutolanil, fluxapiroxad, furametpir, isofetamide, isopirazam, meproxil, penxil, penxil penthiopyrate, sedaxane, teclophthalam, typhusamide, N-(4'-trifluoromethylthiobifene¡I-2¡l)-3-difluorometh¡l-1 -methyl-1 H-pyrazole-4-carboxamide, N-(2-(1,3,3trimethyl-butyl))-pheny-1-3-difluoromethyl-15 H-pyrazol-4-carboxamide, 3-(difluoromethyl)-1 -methyl-N-(1,1,3 -1 ri met i lindane-4-i I) for reason I-4carboxamide, 3-(trifluoromethyl)-1-methyl-N-(1,1,3-trimethylindan-4yl)pyrazole-4-carboxamide, in 1,3-dimethyl-N-(1,1,3-trimethyl¡ndan-4¡l)pyrazole-4-carboxam¡da, 3-(trifluoromethyl)-1,5-dimethyl-N-(1,1,3trimeth¡lindane-4-¡l)pyrazol-4-carboxamide, 1,3,5-trimethyl-N-(1,1,3trimethyl¡ndan-4-¡l)pyrazole-4-carboxamide, N-(7-fluoro-1,1,3-trimethyl¡ nd an-4-i I) -1,3-dimethyl-p¡razol-4-carboxam¡da, N-[2,(24. [2-(2,4-difluorophenyl)phenyl]-3-(difluoromethyl)-1-methylpyrazol-4-carboxamide; N-[2-(2,4-difluorophenyl)phenyl]-3-(trifluoromethyl)pyrazin-2-carboxamide; in synergistically effective amounts.

2. An agricultural mixture according to claim 1, wherein the mixture also comprises at least one insecticidal active compound III selected from group M consisting of the following groups M.1 to M.

1. to MY: M.1 Acetylcholinesterase (AChE) inhibitors of the class of: M.1A carbamates, for example, aldicarb, alanicarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, etiofencarb, fenobucarb, formetanate, furatiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur, thiodicarb, thiophanox, trimetacarb, XMC, xylylcarb and triazamate; or of the class of M.1B organophosphates, for example, acetate, azamethiphos, azinphos-ethyl, azinphos-methyl, cadusafos, chlorethoxyphos, chlorfenvinphos, chlormephos,chlorpyrifos, el o rp ir if o sm eti I o, coumaphos, cyanophos, demeton-S-methyl, diazinon, dichlorvos / DDVP, dicrotophos, dimethoate, dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, famfur, fenamiphos, fenitrothion, fenthion, fosthiazate, heptenofos, imiciafos, isofenfos, isopropyl 0-(methoxyaminothiophosphoryl) salicylate, isoxathion, malathion, mecarbam, methamidophos, methidathion, mevinphos, monocrotophos, naled, omethoate, oxidemetonmethyl, parathion, parathion-methyl, fentoate, phorate, fosalone, fosmet, fosfamidon, phoxim, pirimiphos-methyl, profenophos, propetamphos, protiophos, 140 pyraclophos, pyridafenthion, quinalfos, sulfotep, tebupirimphos, temephos, terbufos, tetrachlorvinphos, thiometon, triazophos, trichlorfon, and vamidothion; M.

2. GABA-regulated chloride channel antagonists, for example: M.2A organochlorine cyclodiene compounds, for example, endosulfan or chlordane; or M.2B fiproles (phenylpyrazoles), for example, etiprole, fipronil, flufiprol,pirafluprol and piriprol; M.3 Class sodium channel modulators: M.3A pyrethroides, for example, acrinathrin, aletrin, d-cis-trans aletrin, d-trans aletrin, bifenthrin, bioalethrin, bioalethrin S-cylclopentenilo, bioresmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cihalothrin, gamma-cihalothrin, cypermethrin, alphacypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin, deltamethrin, empentrin, esfenvalerate, etofenprox, fenpropatrin, fenvalerate, f I ucitrinate, flumethrin, tau-fluvalinate, halfenprox, heptafluthrin, imiprothrin, meperflutrina, metoflutrina, momfluorotrina, permethrin, phenothrin, praletrina, proflutrina, pyrethrin (pyrethrum), resmetrina, silafluofen, teflutrina, tetram et i If I ut ri na, tetrametrina, tralometrina y transflutrina; o M.3B Moduladores del canal de sodio, tales como DDT o metoxicloro; M.4 Agonistas del receptor de acetilcolina nicotínico (nAChR) de la clase de: M.4A neonicotinoides,for example, acteamiprid, c I oti an id ina, cycloxaprid, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam; or the compounds hQA7nn / l 7Π7 / Β / Υ 141 M.4A.2:(2E-)-1 - [(6-chloropyridín-3-¡l)methyl]-N'-nitro-2pentylidenehydrazinecarboximidamide; or M4.A.3:1 - [(6-chlorop¡r¡din-3-¡l)methyl]-7-methyl-8-nitro-5-propoxy¡-1,2,3,5,6,7hexahudroimidazo[1,2-a]pyridine; or nicotine class M.4B; M.5 Allosteric activators of the nicotinic acetylcholine receptor of the spinosine class, e.g., spinosad or spinetoram; M.6 Chloride channel activators of the avermectin and milbemycin class, e.g., abamectin, emamectin benzoate, ivermectin, lepimectin, or milbemectin; M.7 Juvenile hormone mimics, e.g., M.7A juvenile hormone analogues, such as hydroprene, kinoprene, and methoprene; or others, such as M.7B fenoxycarb or M.7C pyriproxyfen; M.8 Miscellaneous non-specific (multi-site) inhibitors, e.g., M.8A alkyl halides,such as methyl bromide and other alkyl halides, or M.8B chloropicrin, M.8C sulfuryl fluoride, M.8D borax or M.8E tartar emetic; M.9 Selective homeopteran feeding blockers, for example, M.9B pymetrozine, or M.9C flonicamid; M.10 Mite growth inhibitors, for example, M.10A clofentezine, hexythiazox, or M.10B etoxazole; hQAJnn / l 7Π7 / Β / ΥΙΛΙ 142 Μ.11 Microbial disruptors of insect midgut membranes, for example bacillus thuringiensis or bacillus sphaericus and the insecticidal proteins they produce, such as bacillus thuringiensis subsp. israelensis, bacillus sphaericus, bacillus thuringiensis subsp. aizawai, bacillus thuringiensis subsp. kurstaki and bacillus thuringiensis subsp. tenebrionis, or the Bt culture proteins: CrylAb, CrylAc, CrylFa, Cry2Ab, mCry3A, Cry3Ab, Cry3Bb and Cry34 / 35Ab1; M.12 Mitochondrial ATP synthase inhibitors, e.g. M.12A diafenthiuron,or M.12B organotin acaricides, such as azocyclotine, cyhexatine or fenbutatin oxide, or M.12C propargite, or M.12D tetradifon; M.13 Uncouplers of oxidative phosphorylation by altering the proton gradient, for example, chlorfenapyr, DNOC or sulfluramid; M.14 Nicotinic acetylcholine receptor (nAChR) channel blockers, for example, nereistoxin analogues, such as bensultap, cartap hydrochloride, thiocyclam or thiosultap sodium; M.15 Chitin biosynthesis type 0 inhibitors, such as benzoylureas, for example, bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron, or triflumuron; M.16 Chitin biosynthesis type 1 inhibitors, for example, buprofezin; M.17 Molting disruptors, Diptera, for example, cyromazine; M.18 Ecdysone receptor agonists, such as diacylhydrazines, for example, methoxyfenozide, tebufenozide,halofenozide, fufenozide or chromafenozide; M.19 Octopamine receptor agonists, for example, amitraz; M.20 Mitochondrial complex III electron transport inhibitors, for example, M.20A hydramethylnon, or M.20B acequinocil, or M.20C f I u acri pi ri m; M.21 Mitochondrial complex I electron transport inhibitors, for example, M.21A METI insecticides and acaricides, such as fenazaquin, fenpyroximate, pirimidifen, pyridaben, tebufenpyrad or tolfenpyrad, or M.21B rotenone; M.22 Voltage-gated sodium channel blockers, for example, M.22A indoxacarb or M.22B metaflumizone or M.22B.1: 2-[2-(4-cyanophenyl)1-[3-(trifluoromethyl)phenyl]ethylen]-N-[4-(difluoromethoxy)phenyl]hydrazincarboxamide or M.22B.2: N-(3-chloro-2-methylphenyl)-2-[(4-chlorophenyl)[4-[methyl(methylsulfonyl)amino]phenyl]methylen]hydrazincarboxamide; M.23 Acetyl CoA carboxylase inhibitors, such as tetronic and tetramic acid derivatives, for example, spirodiclofen,spiromesifen or spirotetramat; M.24 Inhibitors of electron transport of mitochondrial complex IV, for example, M.24A phosphine, such as aluminum phosphide, calcium phosphide, phosphine or zinc phosphide or M.24B cyanide; hQRjnn / i znz / E / YiAi 144 M.25 Inhibitors of electron transport of mitochondrial complex II, such as beta-ketonitrile derivatives, for example, cyenopyrafen or ciflumetofen; M.28 Ryanodine receptor modulators of the diamide class, e.g. flubendiamide, chlorantranil iprole (rynaxypyr®), cyantran iliprole (cyazypyr®) or the phthalamide compounds M.28.1 :(R)-3-chlor-N1-{2-methyl-4-[1,2,2,2 -tetraf I or or-1 (trifl or orm eti I )ethí l]phen i I}-N2-( 1 -methyl-2-methi Isulfo ni I ethyl )phthal amide and M.28.2: (S)-3-chlor-N1-{2-methyl-4-[1,2,2,2 -tetrafluor-1 (trifluoromethyl)ethyl]phenyl}-N2-(1-methyl-2-methylsulfonylethyl)phthalamide or the compound M.28.3:3-bromo-N-{2-bromo-4-chloro-6-[(1 -c¡cloprop¡let¡l)carbamo¡l]phen¡l}1-(3-chlorpyridin-2-¡l)-1 H-pyrazole-5-carboxamide (proposed ISO name: cyclanyl¡proI), or compound M. 28.4: methyl-2-[3,2-dibromo¡-bromo(3-{3-b) -(3-chlorpyrid¡n-2-¡l)-1 Hp¡razol-5-yl]carbon¡l}am¡no)benzo¡l]-1,2-dimethylhydrazine carboxylate; or a selected compound of M.28.5a) to M.28.5I): M.28.5a)N-[4,6-dichloro-2-[(diethyl-lambda-4-sulfanyl¡den)carbamoyl]-phenyl]2-(3-chloro-2-pyr¡d¡l)-5-(trifluoromet¡l)pyrazol-3-carboxam¡da; M.28.5b)N-[4-chloro-2-[(diethyl-lambda-4-sulfan¡l¡dene)carbamo¡l]-6-met¡lphenyl]-2-(3-chloro-2-pyr¡d¡l)-5-(tr¡fluoro methyl I )because l-3-carboxylate; M.28.5c)N-[4-chloro-2-[(di-2-propyl-lambda-4-sulfan¡l¡den)carbamo¡l]-6methyl-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide; M.28.5d)N-[4,6-dichloro-2-[(d¡-2-prop¡l-lambda-4-sulfanyl¡den)carbamo¡l]phenyl]-2-(3-chloro-2-pyr¡d¡l)-5-(tr¡fluoro methi I )pi reason l-3-carboxam ¡da; hQAJnn / l 7Π7 / Β / ΥΙΛΙ 145 M.28.5e)N-[4,6-dichloro-2-[(d¡et¡l-lambda-4-sulfan¡l¡dene)carbamo¡l]-phen¡l]2-(3-chloro-2-p¡r¡d¡l)-5-(difluoromethyl)p¡razol-3-carboxam¡¡¡; M.28.5f)N-[4,6-d¡bromo-2-[(d¡-2-propyl-lambda-4-sulfan¡l¡den)carbamo¡l]phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoro methi I )pi reason l-3-carboxam; M.28.5g) N-[4-chloro-2-[(di-2-propyl-lambda-4-sulfan¡l¡den)carbamo¡l]-6cyano-phen¡l]-2-(3-chloro-2-p¡r¡d¡l)-5-(tr¡fluorometh¡l)p¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡s; M.28.5h)N-[4,6-d¡bromo-2-[(diet¡l-lambda-4-sulfan¡l¡den)carbamo¡l]-phen¡l]2-(3-chloro-2-pyr¡d¡l)-5-(tr¡fluorometrazol)p¡¡fluorometrazol-3-da; M.28.5i)N-[2-(5-amino-1,3,4-thiadiazol-2-¡l)-4-chloro-6-met¡lphen¡l]-3-bromo1 -(3-chloro-2-pyrid¡n¡l)-1 H-pyrazole-5-carboxamide; M.28.5j)3-chloro-1 - (3-chloro-2-pyrid¡n¡l)-N-[2,4-d¡chloro-6-[[(1 -cyano-1 methylethyl)amino]carbonyl]phenyl]-1 H-pyrazol-5-carboxamida; M.28.5k)3-bromo-N-[2,4-dichloro-6-(methylcarbamo¡l)phen¡l]-1 -(3,5-dichloro-2p¡rid i I)-1 H-pyrazol-5-carboxamida; M.28.5l)N-[4-chloro-2-[[(1,1 -dimet¡let¡l)am¡no]carbon¡l]-6-methylphenyl]-1 -(3chloro-2-pyridinyl)-3-(fluoromethoxy)-1 H-pyrazol-5-carboxamida; o un compuesto seleccionado de M.28.6:N-(2-cianopropan-2-yl)-N-(2,4-dimetilfen¡l)-3-¡odobencen-1,2dicarboxamida; o M.28.7:3-cloro-N-(2-cianopropan-2-¡l)-N-(2,4-dimet¡lfen¡l)-bencen-1,2dicarboxamida; M.28.8a)1-(3-cloro-2-p¡rid¡nyl)-N-[4-c¡ano-2-met¡l-6[(meti lamín o)carbon il]f en i I ]-3-[[5-(trifluorometil) -2 H-tetrazol-2-yl]metil]- 1 H-pyrazol-5-carboxamida; or M.28.8b)1 -(3-chloro-2-pyr¡d¡nil)-N-[4-c¡ano-2-methyl-6hQA7nn / l 7Π7 / Β / ΥΙΛΙ 146 [(meth¡lamino)carbonyl]phenyl]-3-[[5-(trifluoromethyl)-1 H-tetrazol-1 -yl]methyl]- 1 H-pyrazol-5-carboxamida; M.UN. Active insecticide compounds with unknown or uncertain method of action, for example, afoxolaner,azadirachtin, amidoflumet, benzoximate, bifenazate, bromopropylate, quinomethionate, cryolite, dicofol, flufenerim, flometoquin, fluensulfone, fluopyram, flupyradifurone, fluralaner, methoxadizone, piperonyl butoxide, piflubumide, pyridalyl, pyriquinazon, sulfoxaflor, thioxazafen, triflumezopyrim, or compounds M.UN.3:11 - (4-chloro-2,6-dimethylphenyl)-1 2-hydroxy-1,4-dioxa-9azadispiro[4.2.4.2]-tetradec-11-en-10-one, or compound M.UN.4:3-(4'-fluoro-2,4-dimethylphenyl-3-1)-4-hydroxy-8-oxa-1 azaspiro[4.5]dec-3-en-2-one, or compound M.UN.5:1-[2-fluoro-4-methyl-5-[(2,2,2-trifluoroethyl)sulfinyl]phenyl]-3(trifluoromethyl)-1H-1,2,4-triazol-5-amine, or actives based on Bacillus firmus (Votive, 1-1582); or a compound selected from group M.UN.6, wherein the compound is selected from M.UN.6a) to M.UN.6k): M.UN.6a)(E / Z)-N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoroacetamide; M.UN. 6b)(E / Z)-N-[1 -[(6-chloro-5-fluoro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2trifluoro-acetamide; M.UN.6c)(E / Z)-2,2,2-trifluoro-N-[1 - [ (6-f I uo ro-3-pyrid i) m ethy I]-2 pi rid i iden] acetam i da; M.UN.6d)(E / Z)-N-[1-[(6-bromo-3-pyridyl)methyl]-2-pyridylidene]-2,2,2trifluoro-acetamide; bQRynn / i znz / B / v 147 M.UN.6e)(E / Z)-N-[1-[1-(6-chloro-3-pyridyl)ethyl]-2-pyridylidene]-2,2,2-trifluoroacetamide; M.UN.6f) (E / Z)-N-[1 -[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2-difluoroacetamide; M.UN.6g)(E / Z)-2-chloro-N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2difluoro-acetamide; M.UN.6h)(E / Z)-N-[1-[(2-chloropyrimidine-5-yl)methyl]-2-pyridylidene]-2,2,2trifluoro-acetamide; M.UN.6i)(E / Z)-N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,3,3,3pentaflu oro-pro pan amide.); M.UN.6j)N-[1 -[(6-chloro-3-pyridl)methl]-2-p¡r¡d¡l¡den]-2,2,2-trifluorothioacetamide or of the compound M.UN.6k)N-[1 -[(6-chloro-3-pyridyl)meth¡l]-2-pyrid¡l¡den]-2,2,2-trifluoro-N'isopropyl-acetamidine or the compounds M. UN. 8:8-chloro-N-[2-chloro-5-methoxyf enyl) su Ifon i]-6-trif luoromethyl) imidazo[1,2-a]pyrid¡n-2-carboxam¡da; o M.UN.9:4-[5-(3,5-dichlorophenyl)-5-(tr¡fluoromethyl)-4H-¡soxazol-3-yl]-2-methylN-(1-oxothiethane-3-yl)benzamide; or M.UN.10:5-[3-[2,6-dichloro-4-(3,3-d¡chloroal¡loxy)phenoxy¡]propox¡]-1 H-pyrazole; or a compound selected from the group of M.UN.11, wherein the compound is selected from M.UN.1 1a) to M.UN.1 1p): M.UN.11 .a)3-[benzoyl(methyl)amino]-N-[2-bromo-4-[1,2,2,2-tetrafluoro-1 (trifluorometh¡l)et¡l]-6-(tr¡fluoromet¡l)phenyl]-2-fluoro-benzamide; M.UN.11.b)3-(benzoylmet¡lamino)-N-[2-bromo-4-[1,2,2,3,3,3-hexafluorobQRynn / i znz / B / v 148 1 -(trifluorometh¡l)prop¡l]-6-(tr¡fluorometh)phenz¡l-2-fln-fluorol-2]; M.UN.11.c)3-(benzoylmethylamine)-2-fluoro-N-[2-odo-4-[1,2,2,2tetrafluoro-1 - (tr¡fluoromethyl)et¡l]-6-(tr¡fluoromethl)phen¡l]-benzam¡da; M.UN.11 .d)N-[3-[[[2-iodo-4-[1,2,2,2-tet raf I u oro -1 - (tr if I uo ro methi I) et i I]-6(tr¡fluorometh¡l)phen¡l]am¡no]carbon¡l]phenyl]-N-meth¡l-benzam¡l; M.UN.11 ,e)N-[3-[[[2-bromo-4-[1,2,2,2-tetrafluoro-1 -(trifluoromethyl)ethyl]-6(trifluoromethyl)phenyl]amino]carbonyl]-2-fluorophenyl]-4-fluoro-N-methylbenzamida; M.UN.11 .f)4-fluoro-N-[2-fluoro-3-[[[2-¡odo-4-[1,2,2,2-tetrafluoro-1 (trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]amino]carbonyl]phenyl]-N-methylbenzamida; M.UN.11 ,g)3-fluoro-N-[2-fluoro-3-[[[2-iodo-4-[1,2,2,2-tetrafluoro-1 (trifluoromet¡l)et¡l]-6-(trifluoromethyl)phenyl]amino]carbonyl]phenyl]-N-methylbenzamida; M.UN.11 ,h)2-chloro-N-[3-[[[2-iodo-4-[1,2,2,2-tetrafluoro-1 (trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]amino]carbonyl]phenyl]-3pyridinecarboxamide; M.UN.11 .i)4-cyano-N-[2-cyano-5-[[2,6-dibromo-4-[1,2,2,3,3,3-hexafluoro1 -(tr¡fluoromet¡l)propyl]phen¡l]carbamo¡l]phen¡l]-2-met¡l-benzamida; M.UN.11 .j)4-cyano-3-[(4-cyano-2-met¡l-benzo¡l)amino]-N-[2,6-dicioro-4[1,2,2,3,3,3-hexafluoro-1 - (trifluoromet¡l)prop¡l]phenyl]-2-fluoro-benzam¡da; M.UN.11 ,k)N-[5-[[2-chloro-6-cyano-4-[1,2,2,3,3,3-hexafluoro-1 (trifluoromethl)prop¡l]phen¡l]carbamo¡l]-2-cano-phen¡l]-4-cano-2-methlbenzamide; M.UN.11 ,l)N-[5-[[2-bromo-6-chloro-4-[2,2,2-trifluoro-1 -hydroxy-1 hQRjnn / i ζηζ / Ε / γ 149 (tr¡fluoromethl)methyl]phen¡l]carbamo¡l]-2-cano-phen¡l]-4-cano-2-methlbenzamide; M.UN.11 .m)N-[5-[[2-bromo-6-chloro-4-[1,2,2,3,3,3-hexafluoro-1 (tr¡fluoromethyl)prop¡l]phen¡l]carbamo¡l]-2-c¡ano-phen¡l]-4-c¡anol-2-benzamida; M.UN.11 .n)4-cyano-N-[2-cyano-5-[[2,6-dichloro-4-[1,2,2,3,3,3-hexafluoro-1 (trifl u oro methyl)propyl]phenyl]carbamo yl]pheny I]-2 - m ethy I-benzamide; M.UN.11 .o)4-cyano-N-[2-cyano-5-[[2,6-d¡chloro-4-[1,2,2,2-tetrafluoro-1 (trifl u oro methyl) ethyl]phen il]carbamoyl]phen i I ] - 2-m et i I-benzamide; M.UN.11 ,p)N-[5-[[2-bromo-6-chloro-4-[1,2,2,2-tetrafluoro-1 (tr¡fluoromethl)ethyl]phen¡l]carbamo¡l]-2-c¡ano-phen¡l]-4-c¡ano-2-benzamida; or a compound selected from the group of M.UN.12, wherein the compound is selected from M.UN.12a) to M.UN.12m): M.UN.12.a) 2-(1,3-d¡oxan-2-¡l)-6-[2-(3-pyrid¡n¡l)-5-t¡azol¡l]-pyrid¡na; M.UN.

12. b) 2-[6-[2-(5-f I uo ro-3-pyridi ni I)-5-ti azo I il]-2-pyridi in I]-pyrimidine; M.UN.12.c) 2-[6-[2-(3-p¡r¡d¡n¡l)-5-t¡azol¡l]-2-pyr¡d¡n¡l]-p¡r¡md¡na; M.UN.12.d) N-methylsulfonyl-6-[2-(3-pyridyl)thiazol-5-yl]pyridin-2-carboxamide M.UN.1 2.e) N-meth¡lsulfon¡l-6-[2-(3-p¡rid¡l)t¡azol-5-l] M.UN.

12. f) N-et¡lN-[4-methyl-2-(3-p¡r¡d¡l)t¡azol-5-¡l]-3-met¡lt¡opropanamide M.UN.1 2.g) N-met¡lN-[4-methyl-2-(3-p¡r¡d¡l)t¡azol-5-¡l]-3-met¡lt¡opropanamide M.UN.1 2. h) N, 2-di methyl -N-[4-methyl-2-(3-pi rid i I )thiazol-5-3-pamethyl-propanamide] hQA7nn / l 7Π7 / Β / Υ 150 M.UN.1 2. i) N-ethyl-2-methyl-N-[4-methyl-2-(3-pyridyl)thiazol-5-¡l]-3-methylthiopropanamide M.UN.1 2. j) N-[4-chloro-2-(3-p¡rdyl)t¡azol-5-¡l]-N-et¡l-2-met¡l-3-met¡lt¡opropanamide M.UN.

12. k) N-[4-chloro-2-(3-pyridyl)thiazol-5-yl]-N,2-dimethyl-3-methylthiopropanamide M.UN.12.1) N-[4-chloro - 2-(3-pyr id i I) ti azo I-5-i I] - N - m et i I-3 - m et i I ti o propanamide M.UN.1 2. m) N-[4-chloro-2-(3-pyrid¡l)thiazol-5-¡l]-N-ethyl-3-methylthiopropanamide; or the compound M.UN.1 3: 2-(4-methoxy¡ i mi nocido hexi 1)-2-(3,3,3trif I uo ro prop i I su If oni I) aceton n ytr i I o; or the compounds M.UN.14a) 1 -[(6-chloro-3-pyridinyl)methyl]-1,2,3,5,6,7-hexahydro-5-methoxy¡-7methyl-8-ni tro-i midazo[1,2-a]pyridine; or M.UN.14b) 1 - [(6-chloropyridin-3-yl)methyl l]-7-methyl I-8-nitro-1,2,3,5,6,7hexahydroim¡dazo[1,2-a]pyridin-5-ol; or the compound M.UN.15:1 - [(2-chloro-1,3-thiazo I - 5-i I) m et i I ]-3-(3,5-dichlor of eni I)-9 - m et i I-4oxo-4H-pyrido[1,2-a]p¡r¡m¡d¡n-1 -io-2-olate; MY Biopesticides, which are pesticide compounds of biological origin with insecticidal, acaricidal, mollucidal and / or nematicidal activity, which includes MY-1: Microbial pesticides: Bacillus firmus, B. thuringiensis ssp. israelensis, B. t. ssp. galleriae,B. t. ssp. kurstaki, Beauveria bassiana, Burkholderia sp., Chromobacterium subtsugae, Cydia bQRynn / i znz / B / v 151 pomonella granulosis virus, Isaria fumosorosea, Lecanicillium longisporum, L. muscarium (formerly Verticillium lecanii), Metarhi varium anisoplie, M. anisoplie. acridum, Paecilomyces fumosoroseus, P. lilacinus, Paenibacillus poppiliae, Pasteuria spp., P. nishizawae, P. reneformis, P. usagae, Pseudomonas fluorescens, Steinernema feltiae, Streptoms galbus; or actives based on bacillus firmus (Votivo®, 1-1582), or MY-2 Biochemical pesticides: L-carvone, citral, (E,Z)7,9-dodecadien-1-yl acetate, ethyl formate, (E,Z)-ethyl decadienoate (2,4-pera), (Z,Z,E)-7,11,13-hexadecatrienal, heptyl butyrate, isopropyl myristate, lavadulyl senecioate, 2-methyl 1-butanol, methyl eugenol, methyl jasmonate, (E,Z)-2,13-octadecadiene-1,2,1,Z 3-octadecadiene-1 -ol, (E,Z)-3,13-octadecadiene-1 - ol, R-1 -octen-3ol, pentatermanone,potassium silicate, sorbitol actanoate, (E,Z,Z)-3,8,11-tetradecatrienyl acetate, (Z,E)-9,1 2-tetradecadien-1-yl acetate, Z-7-tetradecen-2-one, Z-9-tetradecen-1-yl acetate, Z-11-tetradecenal, Z-11-tetradecen-1-ol, black acacia extract, grapefruit seed and pulp extract, Chenopodium ambrosioides extract, catnip oil, neem oil, quillaja extract, marigold oil, or ginkgo tree components selected from the group consisting of bilobalide, ginkgolide A, ginkgolide B, ginkgolide C, ginkgolide J, and ginkgolide M.

3. An agricultural mixture according to claim 1 or 2, wherein the mixture comprises the compound of carboxamide I of formula (I) and one or more fungicidal active compounds and, optionally, one or more insecticidal active compounds.

4. An agricultural mixture according to claims 1, 2 or 3, wherein at least one active compound II is selected from the group consisting of bixafen,boscalid, carboxin, fluopyram, fluxapyroxad, isopyrazam, pentiopyrad, penflufen, and sedaxane.

5. An agricultural mixture according to claims 1, 2, or 3, wherein at least one active compound II is fluxapyroxad.

6. An agricultural mixture according to any one of claims 2 to 20, wherein the additional insecticidal active compound III is fipronil, chlorpyrifos, acetate, methiocarb, tefluthrin, bifenthrin, permethrin, chlorfenapyr, thiodicarb, lambda-cyhalothrin, alpha-cypermethrin, acetamiprid, clothianidin, dinotefuran, imidacloprid, thiacloprid, thiamethoxam, abamectin, emamectin, flubendiamide, spinetoram, spirotetramat, sulfoxaflor, cyflumethophen, flupyradifurone, c I o ran t ran i I ip pro I, N-[4,6dichloro-2-[(d¡ethyl-lambda-4-sulfan¡lden)carbamoyl]-phen¡l]-2-(3-chloro-2pyr¡d¡l)-5-(trifluoromethyl)pyrazole-3-carboxamide,N-[4-chloro-2-[(diethylammbda-4-sulfanilydene)carbamoyl]-6-methyl-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazol-3-carboxamide or N-[4-chloro-2-[(di-2-propyl-lambda-4-sulfanilydene)carbamoyl]-6-methyl-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazol-3-carboxamide or cyantraniliprole.

7. An agricultural mixture according to any one of claims 2 to 5, wherein the additional insecticidal active compound III is methiocarb, thiodicarb, abamectin, emamectin, or flubendiamide.

8. An agricultural mixture according to any one of claims 2 to 5, wherein the additional insecticidal active compound III is lambda-cyhalothrin, tefluthrin, bifenthrin, cypermethrin, or alpha-cypermethrin.

9. An agricultural mixture according to any one of claims 2 to 5, wherein the additional insecticidal active compound III is acetamiprid, clothianidin, dinotefuran, imidacloprid, thiacloprid, or thiamethoxam.

10. An agricultural mixture according to claim 9,wherein the additional insecticidal active ingredient III is thiamethoxam.

11. An agricultural mixture according to any one of claims 2 to 5, wherein the additional insecticidal active ingredient III is chlorantraniliprole, N-[4,6-dichloro-2-[(diethyl-lambda-4-sulfanilidene)carbamoyl]-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazol-3-carboxamide, N-[4-chloro-2-[(diethyl-lambda-4-sulfanilidene)carbamoyl]-6-methylphenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazol-3-carboxamide or N-[4-chloro-2-[(di-2-propyl-lambda-4-sulfanilydene)carbamoyl]-6-methylphenyl]2-(3-chloro-2-pyridine)-5-(trifluoromethyl)pyrazol-3-carboxamide or cyantraniliprole.

12. Agricultural mixtures according to any one of claims 1 to 11, comprising active compound I of Formula I and compound II in a weight ratio of 500:1 to 1:

100.

13. A method for protecting plants against attack or infestation by insects, mites, or nematodes, comprising bringing the plant into contact with,14. A method for controlling insects, arachnids, or nematodes, comprising contacting an insect, mite, or nematode, or its food supply, habitat, breeding site, or locus, with a mixture according to any of claims 1 to 12 in quantities effective as a pesticide.

15. A method for protecting plant propagation material, comprising contacting the plant propagation material with a mixture as defined in any of claims 1 to 12 in quantities effective as a pesticide.

16. Seed, comprising the mixture according to any of claims 1 to 12 in an amount of 0.1 g / 100 kg per 100 kg of seed.

17. A method for controlling harmful phytopathogenic fungi, wherein the fungi,18. A method for protecting plants against phytopathogenic harmful fungi, wherein the fungi, their habitat, or the plants or plant propagation material to be protected against fungal attack, the soil, or the seeds are treated with a fungicidal amount of a mixture of at least one active compound I and at least one active compound II according to any one of claims 1 to 12.

19. Use of a mixture as defined in claims 1 to 12 for combating phytopathogenic harmful fungi. hQA7nn / i ζηζ / E / γ 155 20. Use of a mixture according to any one of claims 1 to 12 for combating insects,arachnids or nematodes.

21. Agricultural composition, comprising a liquid or solid carrier and a mixture according to any of claims 1 to 12.