USE OF ACTIVE CARBOXAMIDE DERIVATIVE AS A PESTICIDE IN SOIL AND SEED APPLICATION AND TREATMENT METHODS

Abstract

The present invention relates to agricultural methods and the use of an active carboxamide derivative as an insecticide in seed treatment and soil application methods. The carboxamide derivative as an insecticide is highly suitable, alone or in combination with other active agricultural ingredients, for controlling animal pests, such as insects, mites, and / or nematodes, by treating the soil / growing substrate through soaking, drip application, immersion, or soil injection.

Description

USE OF ACTIVE CARBOXAMIDE DERIVATIVE AS PESTICIDE IN APPLICATION METHODS AND SOIL AND SEED TREATMENT The present invention relates to the use of carboxamide derivatives to control arthropods, especially insects and arachnids, (spider) mites and / or nematodes. The present invention relates to the use of a carboxamide derivative for controlling soil-dwelling pests by seed treatment methods. The present invention relates to the use of carboxamide derivatives to control soil-dwelling pests by soil application methods, such as drenching, drip application, furrow application, immersion application, or soil injection. or by seed treatment. Invertebrate, arthropod and nematode pests and, in particular, insects and arachnids destroy growing and harvested crops, and attack homes and commercial wooden structures, causing extensive economic losses to food supplies and property. Although a large number of pesticidal agents are known, due to the ability of target pests to develop resistance to such agents, there is a constant need to find new agents to combat invertebrate pests such as insects, arachnids and nematodes. Frequently, soil-dwelling pests, pests of CQQCnn / l 7Π7 / Β / Υ arthropods, including soil-dwelling insects and arachnids, especially spider mites and nematodes, are controlled and controlled by applying an effective amount of a suitable pesticidal compound to the soil, e.g., by drench, drip application, dip application or soil injection. The pesticidal compounds may also be applied as a solid or liquid composition, eg as a granule or powder formulation comprising an inert carrier, eg clay. Ground application methods can have several problems. Pesticidal compounds are not always suitable for application by different soil application methods, such as drench, drip application, dip application or soil injection. In some cases, its pesticidal activity may be affected. Therefore, an object of the present invention is to provide compounds having good pesticidal activity and good applicability in soil treatment techniques against a large number of different invertebrate pests, especially soil-dwelling pests, which are difficult to to control. Some soil-applied pesticide compositions also have the potential to leach. Therefore, care should be taken to minimize contamination of groundwater and surface water. In addition, the effectiveness of the pesticide can vary depending on environmental conditions; For example, a certain amount of rainfall is necessary for the chemical to work properly in the soil, but CQQCnn / l 7Π7 / Β / ΥΙΛΙ too much rain can reduce effectiveness and cause leaks. Therefore, an object of the present invention is to provide compositions that are suitable for combating soil-dwelling pests and that overcome the problems associated with known techniques. In particular, the compositions must be easy to apply and must provide long-lasting action against soil-dwelling pests. Likewise, environmental conditions should not have an adverse effect on the effectiveness of the pesticide. Soil application methods are considered as different techniques of applying pesticide compounds directly or indirectly to the soil and / or on the ground, such as applications by immersion or drip irrigation (on the ground), or injection into the soil. , additional methods of drenching the soil. Other known soil application methods are furrow and T-belt applications. Likewise, an object of the present invention are the methods of application by immersion of roots, tubers or bulbs (called application by immersion), by means of hydroponic systems or also by seed treatment. Another of the problems that the farmer faces in this context is that the seeds, roots and shoots of the plants are constantly threatened by foliar and soil insects and other pests. Therefore, another difficulty in connection with the use of such pesticides for seed protection is that repeated application and CQQCnn / l 7Π7 / Β / ΥΙΛΙ exclusive of an individual pesticide compound, also generates here, in many cases, a rapid selection of soil pests that developed natural or adapted resistance to the active compound in question. Therefore, there needs to be seed protection agents that help prevent or overcome such resistance. Accordingly, another object of the present invention is to provide compounds that solve the problems for the protection of seeds and growing plants, reduce the dose administration rate, improve the spectrum of activity and / or control resistance to pests. Therefore, the present invention also provides methods for the protection of plant propagation material, especially seeds, against soil-dwelling insects, and for protecting the roots and shoots of the resulting plants against foliar and ground-dwelling insects. on the floor. The invention also relates to plant propagation material, especially seeds, which are protected from foliar and soil-dwelling insects. Therefore, in particular, it is an object of the present invention to provide application methods that are suitable for combating soil-dwelling pests. Surprisingly, it has been found that the carboxamide compounds of Formula (I) of the present invention CQQCnn / l 7Π7 / Β / ΥΙΛΙ CQQCnn / l 7Π7 / Β / Υ or the tautomers, enantiomers, diastereomers or salts thereof, are highly suitable for methods to control and / or combat insects, mites and / or nematodes, and especially spider mites, by soil application and seed treatment methods. It has also been found that mixtures of the compound of Formula (I) with other agriculturally active ingredients, such as insecticides or fungicides, are especially suitable for seed treatment. Carboxamide derivatives that generally show pesticidal activity have been previously described. WO200573165 and WO2010018714 describe carboxamide compounds, their preparation and use as pest control agents. WO200701 31 50, JP201 1 -1 57294, JP201 1-157295 and JP201 1-157296 describe mixtures of carboxamides with other active ingredients. The application of some carboxamide derivatives on vegetable seeds was described in JP201 1-157295. However, its surprisingly excellent applicability for soil application techniques and seed treatment methods, and its outstanding activity against soil-dwelling pests, especially in combination with other active ingredients in agriculture, have not been previously described. . formulations The invention also refers to agrochemical compositions suitable for applying in seed treatment methods that comprise an auxiliary and at least the compound of Formula (I) according to the invention. An agrochemical composition comprising a pesticidally effective amount of a compound of Formula (I). The expression "effective amount" indicates an amount of the composition or compounds I, which is sufficient to control harmful pests on cultivated plants or to protect materials, and which does not considerably damage the treated plants. That amount can vary over a wide range and depends on various factors, such as the species of animal pests to be controlled, the crop material or plant treated, climatic conditions, and the specific compound I used. The compounds of Formula (I), their N-oxides and salts can be converted into the usual types of agrochemical compositions, for example solutions, emulsions, suspensions, dusts, powders, pastes, granules, pressed products, capsules and mixtures of these. Examples of composition types are suspensions (eg SC, OD, FS), emulsifying concentrates (eg EC), emulsions (eg EW, EO, ES, ME), capsules (eg CS, ZC ), pastes, tablets, moisturizing powders or dusts (for example, WP, SP, WS, DP, DS), pressed products (for example, BR, TB, DT), granules (for example, WG, SG, GR, FG , GG, MG), insecticidal articles (for example, LN), as well as gel formulations for the treatment of materials of CQQCnn / l 7Π7 / Β / Υ plant propagation, such as seeds (eg GF). These and other composition types are defined in “Catalogue of pesticide formulation types and international coding system”, Technical Monograph No. 2, 6th Edition, May 2008, CropLife International. The compositions are prepared in the known manner, as described by Mollet and Grubemann, Formulation technology, Wiley VCH, Weinheim, 2001; o Knowles, New developments in crop protection product formulation, Agrow Reports DS243, T&F Reports, 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, antifoam agents, colorants, tackifiers and binders. Suitable liquid carriers and solvents are water and organic solvents, such as medium to high boiling point mineral oil fractions, eg kerosene, gas oil; oils of vegetable or animal origin; aliphatic, cyclic and aromatic hydrocarbons, eg toluene, paraffin, tetrahydronaphthalene, alkylated naphthalenes; alcohols, eg ethanol, propanol, butanol, benzyl alcohol, cyclohexanol; glycols; DMSO; ketones, eg cyclohexanone; esters, eg lactates, carbonates, fatty acid esters, gamma-butyrolactone; fatty acids; phosphonates; amines; amides, eg N-methylpyrrolidone, dimethyl fatty acid amides; and mixtures of CQQCnn / l 7Π7 / Β / ΥΙΛΙ these. Suitable solid carriers or fillers are mineral earths, for example silicates, silica gels, talc, kaolin, limestone, quicklime, chalk, clay, dolomite, diatomaceous earth, bentonite, calcium sulphate, magnesium sulphate, magnesium oxide; polysaccharides, eg cellulose, starch; fertilizers, eg ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas; home products CQQCnn / l 7Π7 / Β / ΥΙΛΙ vegetable, eg cereal flour, tree bark flour, wood flour, walnut shell flour and mixtures thereof. Suitable surfactants are surface active compounds, such as anionic, cationic, nonionic and amphoteric surfactants, block polymers, polyelectrolytes and mixtures thereof. Said surfactants can be used as emulsifiers, dispersants, solubilizers, moisturizers, penetration enhancers, protective colloids, or adjuvants. Examples of surfactants are listed in McCutcheon's, Vol.1: Emulsifiers Directories, Glen Rock, USA, American). Anionic Surfactants & Detergents, McCutcheon's 2008 (International ed. or ed. suitable are alkali, alkaline earth or ammonium salts of sulfonates, sulfates, phosphates, carboxylates and mixtures thereof. Examples of sulfonates are alkylaryl sulfonates, diphenyl sulfonates, alpha-olefin sulfonates, lignin sulfonates, sulfonates of fatty acids and oils, ethoxylated alkylphenol sulfonates, alkoxylated arylphenol sulfonates, condensed naphthalene sulfonates, dodecylbenzenes and tridecylbenzenes sulfonates, naphthalene sulfonates us and alkylnaphthalenes, sulfosuccinates, or sulfosuccinamates. Examples of sulfates are sulfates of fatty acids and oils, of ethoxylated alkylphenols, of alcohols, of ethoxylated alcohols or of fatty acid esters. Examples of phosphates are phosphate esters. Examples of carboxylates are alkyl carboxylates, and alcohol carboxylates or alkylphene ethoxylates. Suitable nonionic surfactants are alkoxylated, 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 the alkoxylation, preferably ethylene oxide. Examples of N-substituted fatty acid amines are fatty acid glucamides or fatty acid alkanolamides. Examples of esters are fatty acid esters, glycerol esters or monoglycerides. Examples of sugar-based surfactants are sorbitans, ethoxylated sorbitans, sucrose glucose esters or alkyl polyglucosides. Examples of polymeric surfactants are homopolymers or copolymers of vinylpyrrolidone, vinyl alcohols or vinyl acetate. Suitable cationic surfactants are quaternary surfactants, for example quaternary ammonium compounds with 1 or 2 hydrophobic groups or long chain primary amine salts. Suitable amphoteric surfactants are alkyl betaines and imidazolines. The CQQCnn / l 7Π7 / Β / ΥΙΛΙ suitable block polymers are block polymers of type A-B or AB-A, comprising blocks of polyethylene oxide and polypropylene oxide, or of type A-B-C, comprising alkanol, polyethylene oxide and oxide polypropylene. 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 improve the biological performance of compound I on the target. Examples are surfactants, mineral or vegetable oils, and other auxiliaries. Other examples are listed in Knowles, Adjuvants and additives, Agrow Reports DS256, T&F Reports UK, 2006, Chapter 5. Suitable thickeners are polysaccharides (eg xanthan gum, carboxymethyl cellulose), 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 antifoam agents are silicones, long chain alcohols and fatty acid salts. Suitable colorants (for example, in red, blue or green) are low-hydraulic pigments and water-soluble dyes. Examples are inorganic dyes (for example, iron oxide, titanium oxide, CQQCnn / l 7Π7 / Β / ΥΙΛΙ iron hexacyanoferrate) and organic dyes (for example, alizarin, azo and phthalocyanine dyes). Suitable tackifiers or binders are polyvinylpyrrhoidones, polyvinylacetates, 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 in a purity of 90% to 100%, preferably 95% to 100% (according to the NMR spectrum). Seed treatment solutions (LS), suspoemulsions (SE), flowable concentrates (FS), dry treatment powders (DS), water dispersible suspension treatment powders (WS), water soluble powders (SS) are often ), emulsions (ES), emulsifiable concentrates (EC) and gels (GF) are used for the treatment of plant propagation materials, in particular seeds. The compositions in question produce, after two to ten-fold dilution, active substance concentrations of 0.01 to 60% by weight, preferably 0.1 to 40% by weight, in ready-to-use preparations. The application can be done before or during planting. Methods for applying compound I and its compositions, respectively, to plant propagation material, especially seeds, include coating, coating, pelleting, dusting, soaking and furrowing application methods of the propagation material. Preferably, compound I or its compositions, CQQCnn / l 7Π7 / Β / ΥΙΛΙ respectively, are applied to plant propagation material by a method that does not induce germination, eg by coating, pelleting, coating and seed dusting. When used for plant protection, the amount of active substances applied varies, depending on 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 per ha. For the treatment of plant propagation materials, such as seeds, for example by dusting, coating or soaking in seeds, amounts of active substance of 0.1 to 1000 g, preferably 1 to 1000 g, are generally required with most preferably from 1 to 100 g and most preferably from 5 to 100 g per 100 kilograms of plant propagation material (preferably 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 that are usually applied for the protection of materials are from 0.001 g to 2 kg, preferably from 0.005 g to 1 kg, of active substance per cubic meter of treated material. Various types of oils, humectants, adjuvants, fertilizers or micronutrients and other pesticides (for example, herbicides, insecticides, fungicides, growth regulators, protectants) can be added to the active substances or compositions comprising them, as premixes or, if applicable, just prior to use (tank mix). These agents can be mixed CQQCnn / l 7Π7 / Β / ΥΙΛΙ 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, with a pre-dosing device, a knapsack sprayer, a spray tank, a spray plane or an irrigation system. Frequently, the agrochemical composition is composed of water, buffer and / or other auxiliaries in the desired application concentration and, as a result, the ready-to-use agrochemical composition or spray liquor is obtained. Frequently, 20 to 2000 liters, preferably 50 to 400 liters, of the ready-to-use spray liquor are applied per hectare of usable agricultural area. Applications The present invention relates to methods of use on natural (soil) or artificial (growth) substrates (for example, rock wool, glass wool, quartz sand, gravel, expanded clay, vermiculite), in open or closed systems. (for example, greenhouses or plastic sheeting) and on annual crops (such as vegetables, spices, and ornamentals) or perennial crops (such as citrus, fruits, tropical crops, spices, nuts, vines, conifers, and ornamentals ). It has been discovered that the problems associated with the control of soil-dwelling pests by pesticide treatment of the soil can be solved by such application methods, using the compounds of the present invention. CQQCnn / l 7Π7 / Β / ΥΙΛΙ Animal pests, ie, insects, arachnids and nematodes, the plant, the water or the soil in which the plant grows can be brought into contact with the present Formula I compounds or compositions containing them, by any application method known in the state of the art. As such, contacting includes direct contact (application of compounds / compositions directly to the animal or plant pest) and indirect contact (application of compounds / compositions to the animal or plant pest locus). When contact is made with the plant, in general, contact is made with the tuber, the bulbs or the roots of the plant. The compounds of Formula (I) can also be applied to other parts of the plant, such as leaves, in the case of foliar application, or to plant propagation material, such as seeds, in the case of seed treatment. The compounds of Formula I, or pesticidal compositions comprising them, can be used to protect plants and growing crops from attack or infestation by animal pests, especially insects, mites or arachnids, by contacting the plant / crop with a pesticidally effective amount of the compounds of Formula I. The term "crop" refers to both growing and harvested crops. Therefore, with respect to the use and the object of the present invention, vegetables refer, for example, to vegetables with fruits and inflorescences such as vegetables, for example, pepper, chili, tomato, eggplant, cucumber, pumpkins, zucchini, broad beans. , climbing and dwarf beans, peas, artichoke and corn. Also includes leafy vegetables, such as CQQCnn / l 7Π7 / Β / ΥΙΛΙ head lettuce, radicchio, endive, various types of watercress, rocket, wild lettuce, head lettuce, leek, spinach and chard; Also includes root vegetables, root vegetables, and stem vegetables, such as celeriac / celery, beets, carrots, radishes, horseradish, scorzonera, asparagus, beets for human consumption, hearts of palm, and bamboo shoots. It also includes bulb vegetables, such as onions, leeks, fennel, and garlic. Brassica vegetables, such as cauliflower, broccoli, kohlrabi, red cabbage, white cabbage, kale, savoy cabbage, Brussels sprouts, and bok choy are also vegetables within the meaning of the present application. With respect to the use and purpose of the present invention, perennial crops means citrus fruits, for example, oranges, grapefruits, mandarins, lemons, limes, sour oranges, kinetos, and satsumas. Also pome fruits, such as apples, pears and quinces, and stone fruits, such as peaches, peaches, cherries, plums, quinces and apricots. Also vines, hops, olives, tea and tropical crops such as mangoes, papayas, figs, pineapples, dates, bananas, durians, persimmons, coconuts, cocoa, coffee, avocados, passion fruit and guavas. Also soft fruits, for example, raisins, currants, raspberries, blackberries, black cranberries, strawberries, blueberries, kiwis and lingonberries. Almonds and tree nuts, such as hazelnuts, walnuts, pistachios, cashews, wild chestnuts, pecans, walnuts, chestnuts, hickory nuts, macadamia nuts, and peanuts are also nuts within the meaning of the present invention. . With respect to the use and purpose of the present invention, CQQCnn / l 7Π7 / Β / ΥΙΛΙ ornamental plants means annual and perennial plants, for example, cut flowers, such as roses, carnations, gerberas, lilies, daisies, chrysanthemums, tulips, daffodils, anemones, poppies, amaryllis, dahlias, azaleas, hibiscus, and also, for example, border plants, pot plants and perennials, such as roses, Tagetes, violas, geraniums, fuchsias, hibiscus, chrysanthemums, housewarmings, cyclamen, African violets, sunflowers, begonias. Also, for example, shrubs and conifers, such as ficus, rhododendron, fir, spruce, pine, yew, juniper, meek pine and oleander. With respect to use, spices means annual and perennial plants, such as aniseed, chili peppers, paprika, pepper, vanilla, marjoram, thyme, cloves, juniper berries, cinnamon, tarragon, coriander, saffron, ginger. In addition, the compounds of the present invention and the compositions comprising them are particularly important for the control of multiple insects on various cultivated plants, such as oil crops and cereals, for example, seeds of durum wheat and other types of wheat, barley, oats, rye, corn (fodder corn and sugar corn / sweet and field wheat), soybeans, oil crops, crucifers, cotton, banana, rice, oilseed rape, turnip, sugar beet, fodder beet, brinjal, potato, grass, grass , turf, fodder grass, sugar cane or tobacco. The compounds of the invention can also be applied preventively in places where the existence of pests can be expected. CQQCnn / l 7Π7 / Β / ΥΙΛΙ Locus means the habitat, place of reproduction, plant, seed, soil, area, material or environment in which a pest or parasite develops or can develop. The expression plant propagation material indicates all generative parts of the plant, such as seeds and vegetative material of the plant, such as cuttings and tubers (for example, potatoes), which can be used for the multiplication of the plant. This includes seeds, roots, fruits, tubers, bulbs, rhizomes, shoots, buds, and other parts of plants. Seedlings and young plants that will be transplanted after germination or after emergence from the soil can also be included. These plant propagation materials can be treated prophylactically with a plant protection compound, either before or at the time of planting or transplanting. The term "cultivated plants" includes plants that have been modified by breeding, mutagenesis or genetic engineering. Genetically modified plants are plants whose genetic material has been modified by recombinant DNA techniques which, under natural circumstances, cannot easily be obtained by cross breeding, mutation or natural recombination. In general, one or more genes are integrated into the genetic material of a genetically modified plant in order to improve certain properties of the plant. Such genetic modifications also include, but are not limited to, targeted modification of post-translational protein(s) (oligopeptides or polypeptides), for example, by glycosylation or polymer additions, such as prenylated, acetylated or farnesylated moieties or PEG moieties. (by CQQCnn / l 7Π7 / Β / ΥΙΛΙ example, as described in Biotechnol Prog. 2001 Jul-Aug ;17(4):720-8., Protein Eng Des Sel., 2004 Jan;1 7(1):57 -66, Nat Protocol. 2007;2(5):1225-35., Curr Opin Chem BioL, 2006 Oct;10(5):487-91. Epub, 2006 Aug 28., Biomaterials 2001 Mar;22(5):405-17, Bioconjug Chem. 2005 Jan-Feb;1 6(1):11321). The term "cultivated plants" also includes plants that have been rendered tolerant to applications of specific classes of herbicides, such as hydroxy-phenylpyruvate 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-A0242236, 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 rendered tolerant to herbicides by conventional methods of breeding (mutagenesis), eg Clearfield® summer rapeseed (Cañola) tolerant to imidazolinones, eg imazamox. engineering methods were used CQQCnn / l 7Π7 / Β / ΥΙΛΙ to make cultivated plants, such as soybeans, cotton, corn, beets and rapeseed, tolerant to herbicides such as glyphosate and glufosinate, some of which are commercially available with 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 from Bacillus thuringiensis, such as delta-endotoxins, for example. , CrylA(b), CrylA(c), CrylF, CrylF(a2), CryllA(b), CryllA, CryllIB(b1), or Cry9c; insecticidal vegetative proteins (VIPs), eg, VIP1, VIP2, VIP3 or VIP3A; insecticidal proteins of bacterial colonizing nematodes, eg, Photorhabdus spp. or Xenorhabdus spp.; animal-produced toxins, 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, luphin, saporin or bryodin; steroid metabolism enzymes, such as 3-hydroxysteroid oxidase, ecdysteroid-IDP-glycosyl-transferase, cholesterol oxidases, ecdysone or HMG-CoA-reductase inhibitors; ion channel blockers, such as sodium or calcium channel blockers; CQQCnn / l 7Π7 / Β / ΥΙΛΙ juvenile hormone esterase; diuretic hormone receptors (helicoquin 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 or otherwise modified proteins. Hybrid proteins are characterized by a novel combination of protein domains, (see, for example, WO 02 / 015701). Other 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 person of the medium level trade and are described, for example, in the aforementioned publications. These insecticidal proteins contained in genetically modified plants provide the plants that produce these proteins with protection against harmful pests of certain arthropod taxonomic groups, in particular beetles (Coleoptera), flies (Diptera) and butterflies and moths (Lepidoptera), and nematodes. plant parasites (nematodes). 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 the resistance or tolerance of said plants to bacterial, viral or fungal pathogens. Examples of such proteins are so-called pathogenesis-related proteins (PR proteins, see for example EP-A 0 392 225), genes CQQCnn / l 7Π7 / Β / ΥΙΛΙ resistant to plant diseases (for example, potato cultivars expressing resistance genes against Phytophthora infestans derived from the Mexican wild potato Solanum bulbocastanum) or T4-lysozyme (for example, cultivars of potatoes 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 person of the medium level trade and are described, for example, in the aforementioned publications. 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 (for example, 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 said plants. The expression 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, oily crops that produce fatty acids health-enhancing long-chain omega-3 or unsaturated omega-9 fatty acids (for example, Nexera® rapeseed). The expression cultivated plants also includes plants that CQQCnn / l 7Π7 / Β / ΥΙΛΙ contain, thanks to the use of recombinant DNA techniques, a modified amount of content substances or new content substances, specifically to improve the production of raw materials, e.g. potatoes that produce higher amounts of amylopectin (eg Amflora® potato). In general, pesticidally effective amount means the amount of active ingredient necessary to achieve a significant effect on growth, including the effects of necrosis, killing, retardation, prevention, and elimination, destruction, or otherwise reducing the occurrence and activity of the pest. target organism. The pesticidally effective amount may vary according to the different compounds / compositions used in the invention. A pesticidally effective amount of the compositions will also vary according to prevailing conditions, such as desired pesticidal effect and duration, climate, target species, locus, mode of application, and the like. In the case of soil treatment or application to places or nests where pests inhabit, the amount of active ingredient ranges from 0.0001 to 500 g per 100 m2, preferably 0.001 to 20 g per 100 m2. As mentioned above, soil application methods include, among other known techniques, furrow and T-band applications. The active compound can be applied as a granular application, in a T-band or furrow treatment. Liquid or granular T-belt applications are placed in front of the furrow closing wheels using plastic diffusers. In CQQCnn / l 7Π7 / Β / ΥΙΛΙ Generally, the banded cover pattern is about a couple of inches wide over an open furrow. In the furrows, treatments are directed into the open furrow using plastic tubes. Liquid formulations are applied as T-bands over an open groove. For example, seeds are planted using cone planters, and servitor nozzles are placed over the seed furrow. The boom can be moved up or down to change the bandwidth. A flat vent nozzle can also be used perpendicular to the row of belts and parallel to the row for furrow application. The boom position is located between the furrow opener and the press wheel which directs part (band) or all (in furrow) of the spray into the furrow before closing it. When used in furrow applications, the active compound can be applied simultaneously with seed planting, for example, as granular, liquid or other formulation types. Alternatively, the nozzles can be positioned behind the press wheel for complete spraying of the surface of the liquid formulation, comprising the active compounds. The compounds of Formula I are suitable for seed treatment in order to protect the seed from insect pests, in particular from soil-dwelling insect pests, and the resulting roots and shoots of the plant from pests that live in the soil and CQQCnn / l 7Π7 / Β / ΥΙΛΙ Foliar Insects. The compounds of Formula I are particularly useful for the protection of seeds from soil-dwelling pests, and the resulting roots and shoots of the plant from soil-dwelling pests and foliar insects. Protection of the roots and resulting shoots of the plant is preferred. The protection of the shoots resulting from the plant against incisive and sucking insects is more preferred; protection against aphids is most preferred. Therefore, the present invention comprises a method for the protection of seeds against insects, in particular, against insects living in the soil, and for the protection of the roots and shoots of the seedling against insects, in particular, against foliar and soil-dwelling insects, wherein said method comprises contacting the seeds before sowing and / or after pregermination with a compound of general Formula I or its salt. In particular, a method by which the roots and shoots of the plant are protected is preferred, more preferably a method by which the shoots of the plants are protected against incisive and sucking insects, most preferably a method by which plant shoots are protected against aphids. The term seed'1 includes all types of seeds and plant propagules, including, but not limited to, true seeds, seed parts, suckers, corms, bulbs, fruits, tubers, kernels, cuttings, cut shoots, and the like, and in a form of preferred embodiment, means true seeds. The expression seed treatment includes all the CQQCnn / l 7Π7 / Β / ΥΙΛΙ 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 encompasses seeds coated with the active compound or containing the active compound. In general, the term coated and / or containing means that the active ingredient is mainly on the surface of the propagation product at the time of application, although a greater or lesser part of the ingredient may penetrate the propagation product, depending on the application method. When the propagation product is (re)planted, it can absorb the active ingredient. Suitable seeds are cereal seeds, root crops, oil crops, vegetables, spices, ornamentals, for example durum and other wheat seed, barley, oats, rye, corn (feed corn and corn / wheat sugar sweet and field), soybeans, oil crops, crucifers, cotton, sunflower, banana, rice, oilseed rape, turnip, sugar beet, fodder beet, eggplant, potato, pasture, grass, turf, fodder grass, tomato, leek, squash / Pumpkin, cabbage, iceberg lettuce, pepper, cucumber, cantaloupe, Brassica species, cantaloupe, beans, peas, garlic, onion, carrot, tuberous plants such as potatoes, sugarcane, tobacco, grapevine, petunia, geranium / pelargonium, thoughts and impatiens In addition, the active compound can also be used for the treatment of seeds of plants that tolerate the action of herbicides or fungicides or insecticides that is due to reproduction, which includes the CQQCnn / l 7Π7 / Β / ΥΙΛΙ genetic engineering methods. For example, the active compound can be used in the treatment of plant seeds, which are resistant to herbicides from the group consisting of sulfonylureas, imidazolinones, glufosinato-ammonium or glyphosate-isopropylammonium and analogous active substances (see, for example, EP- A-0242236, EP-A-242246) (WO 92 / 00377) (EP-A-0257993, US 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 plants resistant to certain pests (EP-A-0142924, EP-A0193259), In addition, the active compound can also be used for the treatment of plant seeds, which 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 recombinant procedures). For example, several cases of recombinant modifications of crop plants have been described in order to modify the starch synthesized in plants (for example, WO 92 / 1 1376, WO 92 / 14827, WO 91 / 19806) or crop plants. transgenics having a modified fatty acid composition (WO 91 / 13972). The application of the seed treatment of the active compound is carried out by spraying or dusting the seeds before sowing of the plants and before the emergence of the plants. Compositions that are especially useful for seed treatment are, for example: CQQCnn / l 7Π7 / Β / ΥΙΛΙ A Soluble concentrates (SL, LS) 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 dusts (DP, DS) Conventional seed treatment formulations include, for example, flowable concentrates FS, solutions LS, dry treatment powders DS, water-dispersible suspension treatment powders WS, water-soluble powders SS and emulsions ES and EC, and gel formulations GF. These formulations can be applied diluted or undiluted to the seed. The application to the seeds is carried out before sowing, either directly on the seeds or after their pre-germination. In a preferred embodiment, an FS formulation is used for seed treatment. Typically an FS formulation may comprise 1-800g / l active ingredient, 1-200g / l surfactant, 0-200g / l antifreeze agent, 0-400g / l binder, 0 to 200 g / l of a pigment and up to 1 liter of a solvent, preferably water. In general, especially preferred FS formulations of the compounds of Formula I for seed treatment comprise 0.1 to 80% by weight (1 to 800 g / l) of active ingredient, 0.1 to 20% by weight (1 to 200 g / l) of at least one surfactant, for example 0.05 CQQCnn / l 7Π7 / Β / ΥΙΛΙ to 5% by weight of a humectant and from 0.5 to 15% by weight of a dispersing agent, up to 20% by weight, for example, from 5 to 20% of an antifreeze agent, from 0 to 15% by weight, for example from 1 to 15% by weight of a pigment and / or a dye, from 0 to 40% by weight, for example from 1 to 40% by weight of a binder of tack / adhesion), optionally up to 5% by weight, for example 0.1 to 5% by weight of a thickener, optionally 0.1 to 2% of an antifoam 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 / carrier up to 100% by weight. Seed treatment formulations may also contain binders and, optionally, colorants. Binders can be added to improve the adhesion of the active materials on the seeds after treatment. Suitable binders are homo- and copolymers of alkylene oxides, such as ethylene oxide or propylene oxide, po I i vi n i lacetate, polyvinyl alcohols, po I i vi n i I pyrro I id o n as and their copolymers, copolymers of ethylene vinyl acetate, acrylic homo- and copolymers, polyethyleneamines, polyethyleneamides and polyethyleneimines, polysaccharides such as celluloses, tylose and starch, polyolefin homo- and copolymers such as olefin / maleic anhydride copolymers, polyurethanes, polyesters, homo- and copolymers of polystyrene. Optionally, colorants can also be included in the formulation. Dyes or dyes suitable for seed treatment formulations Rhodamine B, C.l. Red pigment 112, C.l. CQQCnn / l 7Π7 / Β / ΥΙΛΙ 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, Pigment Red 48:1, Pigment Red 57:1, Pigment Red 53:1, Pigment Orange 43, Pigment Orange 34, Pigment Orange 5, Pigment Green 36, Pigment Green 7, Pigment White 6, Pigment Brown 25, Basic Violet 10, basic violet 49, acid red 51, acid red 52, acid red 14, acid blue 9, acid yellow 23, basic red 10, basic red 108. An example of a gelling agent is carrageenan (Satiagel®). For seed treatment, the application rates of compounds I generally range from 0.1 g to 10 kg per 100 kg of seeds, preferably from 1 g to 5 kg per 100 kg of seeds, more preferably from 1 g to 1000 g per 100 kg of seed and, in particular, from 1 g to 200 g per 100 kg of seed. Therefore, the invention also relates to seeds comprising a compound of Formula (I) or an agriculturally useful salt of I, as defined herein. In general, the amount of compound I or its salt useful in agriculture ranges from 0.1 g to 10 kg per 100 kg of seeds, preferably from 1 g to 5 kg per 100 kg of seeds, in particular from 1 g to 1000 g per 100 kg of seeds. For specific crops, such as lettuce, the rate may be higher. pests and fungi In particular, the invention relates to soil application methods for combating soil-dwelling nematode pests and arthropod pests, comprising applying to the soil an amount CQQCnn / l 7Π7 / Β / ΥΙΛΙ effective as a pesticide of a compound of the present invention. The expression "soil-inhabiting" means that the habitat, area, environment or breeding place where the pest or parasite grows or can grow is the soil. The use of the compounds according to the present invention extends to a wide range of different animal pests, especially soil-dwelling pests. These include, among others, the following families: insects of the order Lepidoptera (Lepidoptera), for example, Agrotis ypsilon, Agrotis segetum, Alabama argillacea, Anticarsia gemmatalis, Argyresthia conjugella, Autographa gamma, Bupalus piniarius, Cacoecia murinana, Capua reticulana, Cheimatobia brumata, Choristoneura fumiferana, Choritoneura occidentalis, Cirphis unipuncta, Cydia pomonella, Dendrolimus pini, Diaphania nitidalis, Diatraea grandiosella, Earias insulana, Elasmopalpus lignosellus, Eupoecilia ambiguella, Evetria bouliana, Feltia subterranean, Galleria mellonella, Grapholitha funebrana, Grapholitha molesta, Heliothis armigera, Heliothis virescens, Heliothis zea, Hellula undalis, Hibernia defoliaria, Hyphantria cunea, Hyponomeuta malinellus, Keiferia lycopersicella, Lambdina fiscellaria, Laphygma exigua, Leucoptera coffeella, Leucoptera scitella, Lithocolletis blancardella, Lobesia botrana, Loxostege sticticalis, Lymantria dispar, Lymantria monacha, Lyonetia clerkella, Malacosoma neustria, Mamestra brassicae, Orgyia pseudotsugata , Ostrinia nubilalis, Panolis flammea, Pectinophora gossypiella, Peridroma saucia, Phalera bucephala, Phthorimaea operculella, Phyllocnistis citrella, Pieris CQQCnn / l 7Π7 / Β / ΥΙΛΙ brassicae, Plathypena scabra, Plutella xylostella, Pseudoplusia includens, Fíhyacionia frusrana, Scrobipalpula absoluta, Sitotroga cerealella, Sparganothis pilleriana, Spodoptera frugiperda, Spodoptera littoralis, Spodoptera litura, Thaumatopoea Pityocampa, Tortrix viridana, Trichoplusia ni, Tuta absoluta, and Zeiraphera canadensis; beetles {Coleoptera), for example, Agrilus sinuatus, Agriotes lineatus, Agriotes obscurus, Amphimallus solstitialis, Anisandrus dispar, Anoplophora glabripensis, Anthonomus grandis, Anthonomus pomorum, Aphthona euphoridae, Athous haemorrhoidalis, Atomaria linearis, Blastophagus piniperda, Blitophaga undata, Byctiscus betulae, Cassida nebulosa, Cerotoma trifurcata, Cetonia aurata, Ceuthorrhynchus assimilis, Ceuthorrhynchus napi, Chaetocnema tibialis, Conoderus vespertinus, Crioceris asparagi, Ctenicera ssp., Diabrotica longicornis, Diabrotica semipunctata, Diabrotica 12-punctata Diabrotica spe ciosa, Diabrotica virgifera, Epilachna varivestis, Epitrix hirtipennis, Hylobius abietis, Hypera brunneipennis, Hypera postica, Ips typographus, Lema bilineata, Lema melanopus, Leptinotarsa ​​decemlineata, Limonius californicus, Lissorhoptrus oryzophilus, Melanotus communis, Meligethes aeneus, Melolontha hippocastani, Melolontha, Oulema oryzae, Otiorrhy nchus suicatus, Otiorrhynchus ovatus, Phaedon cochleariae, Phyllobius pyri, Phyllotreta chrysocephala, Phyllophaga sp., Phyllopertha horticola, Phyllotreta nemorum, Phyllotreta striolata, Popillia japonica, Sitona lineatus; and, flies, mosquitoes (Diptera), eg Ceratitis capitata, Contarinia sorghicola Dacus cucurbitae, Dacus oleae, Dasineura CQQCnn / l 7Π7 / Β / ΥΙΛΙ brassicae, Delia antique, Delia coarctata, Delia platura, Delia radicum, Liriomyza sativae, Liriomyza trifolii, Oscinella frit, Pegomya hysocyami, Phorbia antiqua, Phorbia brassicae, Phorbia coarctata, Psila rosae, Psorophora discolor, fiha goletis cerasi, Rhagoletis pomonella, Típula oleracea and Típula paludosa; Thrips (Thysanoptera), for example Dichromothrips corbetti, Dichromothrips ssp., Frankliniella fusca, Frankliniella occidentalis, Frankliniella tritici, Scirtothrips citri, Thrips oryzae, Thrips palmi and Thrips tabaci; termites (Isoptera), for example Calotermes flavicollis, Leucotermes flavipes, Heterotermes aureus, Reticulitermes flavipes, Reticulitermes virginicus, Reticulitermes lucifugus, Reticulitermes santonensis, Reticulitermes grassei, Termes natalensis and Coptotermes formosanus; Bugs, aphids, cicadas, whiteflies, mealybugs, cicadas (Hemiptera), e.g. Acrosternum hilare, Blissus leucopterus, Cyrtopeltis notatus, Dysdercus cingulatus, Dysdercus intermedius, Eurygaster integriceps, Euschistus impictiventris, Leptoglossus phyllopus, Lygus lineolaris, Lygus pratensis, Nezara viridula, Piesma quadrata, Solubea insularis, Thyanta perditor, Acyrthosiphon onobrychis, Adelges laricis, Aphidula nasturtii, Aphis fabae, Aphis forbesi, Aphis pomi, Aphis gossypii, Aphis grossulariae, Aphis schneideri, Aphis spiraecola, Aphis sambuci , Acyrthosiphon pisum, Aulacorthum solani, Bemisia argentifolii, Brachycaudus cardui, Brachycaudus helichrysi, Brachycaudus persicae, Brachycaudus prunicola, Brevicoryne brassicae, Capitophorus CQQCnn / l 7Π7 / Β / ΥΙΛΙ horni, Cerosipha gossypii, Chaetosiphon fragaefolii, Cryptomyzus ribis, Dreyfusia nordmannianae, Dreyfusia piceae, Dysaphis radicóla, Dysaulacorthum pseudosolani, Dysaphis plantaginea, Dysaphis pyri, Empoas ca fabae, Euschistos heros, Euschistos servus, Haiyomorpha halys, Hyalopterus pruni, Hyperomyzus lactucae, Macrosiphum avenae, Macrosiphum euphorbiae, Macrosiphon rosae, megacopta criberia, Megoura viciae, Melanaphis pyrarius, Metopolophium dirhodum, Myzus persicae, Myzus ascalonicus, Myzus cerasi, Myzus variaos, Nasonovia ribis-nigri, Nezara viridula , Nilaparvata lugens, Pemphigus bursarius, Perkinsiella saccharicida, Phorodon humuli, Psylla mali, Psylla piri, Rhopalomyzus ascalonicus, Rhopalosiphum maidis, Rhopalosiphum padi, Rhopalosiphum insertum, Sappaphis mala, Sappaphis mali, Schizaphis graminum, Schizoneura lanuginosa, Sitobion avenae, Triale urodes vaporariorum, Toxoptera aurantiiand, Viteus vitifolii, Cimex lectularius, Cimex hemipterus, Reduvius senilis, Triatoma spp. and Arilus critatus; ants, bees, wasps, sawflies (Hymenoptera), e.g. Athalia rosae, Atta cephalotes, Atta capiguara, Afta cephalotes, Afta laevigata, Atta robusta, Atta sexdens, Atta texana, Crematogaster spp., Hoplocampa minuta, Hoplocampa testudinea, Lasius niger, Monomorium pharaonis, Solenopsis geminata, Solenopsis invicta, Solenopsis richteri, Solenopsis xyloni, Pogonomyrmex barbatus, Pogonomyrmex californicus, Pheidole megacephala, Dasymutilla occidentalis, Polistes rubiginosa, Camponotus floridanus and Linepithema humile; crickets, grasshoppers, locusts (Orthoptera), eg Acheta CQQCnn / l 7Π7 / Β / ΥΙΛΙ domestica, Gryllotalpa gryllotalpa, Locusta migratoria, Melanoplus bivittatus, Melanoplus femurrubrum, Melanoplus mexicanus, Melanoplus sanguinipes, Melanoplus spretus, Nomadacris septemfasciata, Schistocerca americana, Schistocerca gregaria, Dociostaurus maroccanus, Tachycines asynamorus, Oedaleus senegalensis, Zonozerus variegatus, Hieroglyphus daganensis, Kraussaria angulitera, Calliptamus italicus, Chortoicetes terminifera and Locustana pardalina; Arachnoidea, such as arachnids / Acariña), for example from the families Argasidae, Ixodidae and Sarcoptidae, such as Amblyomma americanum, Amblyomma variegatum, Ambryomma maculatum, Argas persicus, Boophilus annulatus, Boophilus decoloratus, Boophilus microplus, Dermacentor silvarum, Dermacentor a ndersoni, Dermacentor variabilis, Hyalomma truncatum, Ixodes ricinus, Ixodes rubicundus, Ixodes scapularis, Ixodes holocyclus, Ixodes pacificus, Ornithodorus moubata, Ornithodorus hermsi, Ornithodorus turicata, Ornithonyssus bacoti, Otobius megnini, Dermanyssus gallinae, Psoroptes ovis, Rhi Picephalus sanguineus, Rhipicephalus appendiculatus, Rhipicephalus evertsi , Sarcoptes scabiei and Eriophyidae spp., such as Aculus schlechtendali, Phyllocoptrata oleivora and Eriophyes sheldoni; Tarsonemidae spp., such as Phytonemus pallidus and Polyphagotarsonemus latus; Tenuipalpidae spp., such as Brevipalpus phoenicis; Tetranychidae spp., such as Tetranychus cinnabarinus, Tetranychus kanzawai, Tetranychus pacificus, Tetranychus telarius and Tetranychus urticae, Panonychus ulmi, Panonychus citri and Oligonychus pratensis; Araneida, for example, Latrodectus mactans and Loxosceles reclusa. CQQCnn / l 7Π7 / Β / ΥΙΛΙ Other animal pests that can be controlled and combated with the methods of the present invention are: From the Pemphigidae family: Eriosoma spp., Pemphigus spp., Anuraphis spp., Brachycaudus spp., in crops such as pome fruits, conifers, vegetables and ornamental plants. From the psyllid family (Psyllidae: Psylla spp., Paratrioza spp., Trioza spp., in crops such as citrus, vegetables, potatoes and pome fruits. From the mealybug family (Coccidae): Ceroplastes spp., Drosicha spp. Pulvinaria spp., Protopuhninaria spp., Saissetia spp., Coccus spp., in perennial crops, such as citrus, vines, tea, pome fruits and stone fruits, tropical crops, ornamental plants, conifers, and also vegetables. From the Diaspididae family: Quadraspidiotus spp., Aonidiella spp., Lepidosaphes spp., Aspidiotus spp., Aspis spp., Diaspis spp., Parlatoria spp., Pseudaulacaspis spp., Unaspis spp., Pinnaspis spp., Selenaspidus spp., in crops, such as citrus, tea, ornamentals, conifers, pome and stone fruits, vines and tropical fruits. From the Pseudococcidae family: Pericerga, Pseudococcus spp., Planococcus spp., Phenacoccus spp., Dysmicoccus spp., in crops such as citrus, pome fruits and stone fruits, tea, vines, vegetables, ornamental plants, conifers, spices and tropical crops. In addition, from the Aleyrodidae family: Bemisia argentifolii, Bemisia tabaci, Trialeurodes vaporariorum, Aleurothrixus floccosus, Aleurodes spp., Dialeurodes spp., Parabemisia myricae in crops, such as CQQCnn / l 7Π7 / Ε / ΥΙΛΙ vegetables, melons, potatoes, tobacco, soft fruits, citrus, ornamental plants, conifers, cotton, potatoes and tropical crops. Also, from the family Aphidae: Myzus spp. in tobacco, stone fruit, pome fruit, soft fruit, Brassica vegetables, fruit-bearing vegetables, leafy vegetables, tuber and root vegetables, melons, potatoes, spices, ornamentals, and conifers. Aphis spp. in cotton, tobacco, citrus, melons, beets, soft fruits, oilseed rape, fruiting vegetables, leafy vegetables, Brassica vegetables, tuber and root vegetables, ornamentals, potatoes, squash, and spices. Rhodobium porosum in strawberries, Nasonovia ribisnigri on leafy vegetables, Macrosiphum spp. on ornamental plants, cereals, potatoes, leafy vegetables, Brassica vegetables and fruiting vegetables, strawberries, Phorodon humuli on hops, Toxoptera spp. in citrus fruits, stone fruits, almonds, dried fruits, cereals and spices; Aulacorthum spp. on citrus, potatoes, fruit-bearing vegetables, and leafy vegetables. In addition, the following species of the family Tetranychidae: Tetranychus spp., Brevipalpus spp., Panonychus spp., Oligonycbus spp., Eotetranychus spp., Bryobia spp. in crops, such as vegetables, ornamental plants, spices, conifers, citrus, stone fruits and pome fruits, vines, cotton, soft fruits, melons, potatoes. The following species of the family Tarsonemidae: CQQCnn / l 7Π7 / Β / ΥΙΛΙ Hermitarsonernus batus, Stenotarsonemus spp., Polyphagotarsonemus spp., Stenotarsonemus spinki in crops, such as vegetables, ornamentals, spices, conifers, tea, citrus, and melons. In addition, the following species of the thrip family (Thripidae): Anaphothrips spp., Baliothrips spp., Caliothrips spp., Frariklirúella spp., Heliothrips spp., Hercrnothrips spp., Rhipiphorothrips spp., Scirtothrips spp., Selenothrips spp. and Thrips spp., on crops such as fruits, cotton, vines, soft fruits, vegetables, melons, ornamentals, spices, conifers, tropical crops, and tea. In addition, the following species of the whitefly family (Agromyzidae): Liriomyza spp., Pegomya spp. in crops, such as vegetables, melons, potatoes and ornamental plants. Also the following species of the family of foliar nematodes (Aphelenchoididae), eg Aphelenchoides ritzemabosi, A. fragariae, A. besseyi, A. blastophthorus in crops, such as soft fruit and ornamental plants. The methods of the present invention are applied to control and combat arachnids, especially the following species of the Tetranychidae family: Tetranychus spp., Brevipalpus spp., Panonychus spp., Oligonycbus spp., Eotetranychus spp. and Bryobia spp. When combined with fungicidal active ingredients in the methods according to the present invention, mixtures of the compound of Formula I are furthermore especially suitable for combating fungal infections. CQQCnn / l 7Π7 / Β / ΥΙΛΙ phytopathogenic fungi effectively. These mixtures have excellent activity against a broad spectrum of phytopathogenic fungi Ascomycetes, Basidiomycetes, Deuteromycetes and Peronosporomycetes (syn. Oomycetes). Some of them are systemically effective and can be used for crop protection as foliar fungicides, seed coat fungicides, and soil fungicides. They can also be used to treat seeds. These mixtures are particularly important in the control of multiple fungi on various crop plants, such as wheat, rye, barley, oats, rice, corn, grasses, bananas, cotton, soybeans, coffee, sugar cane, vines, fruits, and ornamentals. , and vegetables, such as cucumbers, beans, tomatoes, potatoes, and cucurbits, 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 (eg, A. candida), and sunflowers (eg, A. tragopogonis); Alternaria spp. (Alternaria leaf spot) on vegetables, rapeseed (A. brassicola or brassicae), sugar beet (A. tenuis), fruits, rice, soybeans, potatoes (for example, A. solani or A. alternata), tomatoes (for example, example, A. solani or A. alternata) and wheat; Aphanomyces spp. in sugar beets and vegetables; Ascochyta spp. in cereals and vegetables, for example, A. tritici (anthracnose) in wheat and A. hordei in barley; Bipolaris and Drechslera spp. (teleomorph: Cochliobolus spp.), e.g. Southern leaf blight (D. maydis) or Northern leaf blight (B. zeicola) on maize, e.g. CQQCnn / l 7Π7 / Β / ΥΙΛΙ spot (B. sorokiniana) on cereals and, for example, B. oryzae on rice and grass; Blumeria (formerly Erysiphe) graminis (powdery mildew) on cereals (eg, on wheat or barley); Botrytis cinerea (teleomorph: Botryotinia fuckeliana: gray mold) on fruits and berries (eg strawberries), vegetables (eg lettuce, carrots, celery and cabbage), rapeseed, flowers, vines, forest plants and wheat; Bremia lactucae (m i Idi ú) in lettuce; Ceratocystis (syn. Ophiostoma) spp. (rot or wilt) on broadleaf and evergreen trees, eg C. ulmi (Dutch elm disease) on elms; Cercospora spp. (Cercospora leaf spot) on corn (eg, gray leaf spot: C. zeae-maydis), rice, sugar beet (eg, C. beticola), sugarcane, vegetables, coffee, soybean (eg, C . sojina or C. kikuchii) and rice; Cladosporium spp. on tomatoes (eg C. fulvum: leaf mold) and cereals, eg C. herbarum (black head) on wheat; Claviceps purpurea (ergot) in cereals; Cochliobolus (anamorph: Bipolaris Helminthosporium) spp. (leaf spots) on maize (C. carbonum), cereals (eg C. sativus, anamorph: B. sorokiniana) and rice (eg C. miyabeanus, anamorph: H. oryzae); Colletotrichum (teleomorph: Glomerella) spp. (anthracnose) on cotton (eg, C. gossypii), corn (eg, C. graminicola: anthracnose stem rot), soft fruit, potatoes (eg, C. coccodes: black spot), beans (eg, C. lindemuthianum) and soybean (eg, C. truncatum or C. gloeosporioides); Corticium spp., eg C. sasakii (sheath blight) on rice; Corynespora cassiicola (leaf spots) on soybean and ornamentals; Cycloconium spp., by CQQCnn / l 7Π7 / Β / ΥΙΛΙ example, C. oleaginum on olive trees; Cylindrocarpon spp. (eg, fruit tree canker or young vine blight, teleomorph: Nectria or Neonectria spp.) on fruit trees, vines (eg, C. liriodendri, teleomorph: Neonectria liriodendri·. Blackfoot Disease) and ornamentals; Dematophora (teleomorph: Rosellinia) necatrix (root and stem rot) on soybean; Diaporthe spp., eg D. phaseolorum (drop) on soybean; Drechslera (syn. Helminthosporium, teleomorph: Pyrenophora) spp. on corn, cereals, such as barley (eg, D. teres, net spot) and wheat (eg, D. tritici-repentis: brown spot), rice, and grass; Scar (dieback, apoplexy) in vines, caused by Formitiporia (syn. Phellinus) punctata, F. mediterranean, Phaeomoniella chlamydospora (early Phaeoacremonium chlamydosporum), 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 soot) on rice; Epicoccum spp. (black mold) on wheat; Erysiphe spp. (powdery mildew) on sugar beet (E. betae), vegetables (eg E. pisi), such as cucurbits (eg E. cichoracearum), cabbage, rapeseed (eg E. cruciferarum); Eutypa lata (Eutypa ulcer or dieback, anamorph: Cytosporina lata, syn. Libertella blepharis) on fruit trees, vines, and ornamental woodlands; Exserohilum (syn. Helminthosporium) spp. on corn (eg, E. turcicum); Fusarium (teleomorph: Gibberella) spp. (wilt, root or stem rot) on various plants, such as F. graminearum or F. culmorum (root rot, scab or blight CQQCnn / l 7Π7 / Β / ΥΙΛΙ from the top) on cereals (for example, wheat or barley), F. oxysporum on tomatoes, F. sotani (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 corn; Gaeumannomyces graminis (take-all) in cereals (for example, in wheat or barley) and maize; Gibberella spp. on cereals (eg G. zeae) and rice (eg G. fujikuroi: Bakanae disease); Glomerella cingulata on vines, pome fruit, and other plants, and G. gossypii on cotton; grain staining complexes in rice; Guignardia bidwellii (black rot) on vines; Gymnosporangium spp. on rosaceous plants and junipers, eg, G. sabinae (rust) on pears; Helminthosporium spp. (syn. Drechslera, teleomorph: Cochliobolus) in maize, cereals and rice; Hemileia spp., eg, H. vastatrix (coffee leaf rust) on coffee; Isariopsis clavispora (syn. Cladosporium vitis) on vines; Macrophomina phaseolina (syn. phaseoli) (root and stem rot) on soybean and cotton; Microdochium (syn. Fusarium) nivale (pink snow mold) on cereals (eg wheat or barley); Microsphaera diffusa (powdery mildew) on soybean; Monilinia spp., eg, M. laxa, M. fructicola and M. fructigena (flower and twig blight, brown rot) on stone fruits and other rosaceous plants; Mycosphaerella spp. on cereals, bananas, soft fruits and nuts, such as, for example, M. graminicola (anamorph: Septoria tritici, Septoria spot) on wheat or M. fijiensis (black Sigatoka disease) on bananas; Peronospora spp. (powdery mildew) on cabbage (for example, P. brassicae), rapeseed (for example, P. parasitica), onion (for example, P. destructor), tobacco (P. tabacina), and soybean (for example, P. CQQCnn / l 7Π7 / Β / ΥΙΛΙ manshurica); Phakopsora pachyrhizi and P. meibomiae (soybean rust) in soybean; Phialophora spp. eg on vines (eg P. tracheiphila and P. tetraspora) and soybeans (eg P. gregata: stem rot); Phoma lingam (root and stem rot) on rapeseed and cabbage, and P. betae (root rot, leaf spot and drop) on sugar beet; Phomopsis spp. on sunflowers, grapevines (eg, P. viticola·. can and leaf spot) and soybeans (eg, stem rot: P. phaseoli, teleomorph: Diaporthe phaseolorum); Physoderma maydis (brown spots) on corn; Phytophthora spp. (withering, root, leaf, fruit, and stem rot) in various plants, such as paprika and cucurbits (eg, P. capsici), soybeans (eg, P. megasperma, syn. P. sojae), potatoes, and tomatoes (eg P. infestans: late blight) and broadleaf trees (eg P. ramorum: sudden death oak); Plasmodiophora brassicae (club root) on cabbage, rapeseed, radish and other plants; Plasmopara spp., for example, P. viticola (vine grapevine) on vines and P. halstedii on sunflowers; Podosphaera spp. (powdery mildew) on rosaceous plants, hops, knobs and soft fruits, eg P. leucotricha on apple; Polymyxa spp., for example, on cereals, such as barley and wheat (P. graminis) and sugar beet (P. betae) and thus transmitted viral diseases; Pseudocercosporella herpotrichoides (eyespot, teleomorph: Tapesia yallundae) on cereals, eg wheat or barley; Pseudoperonospora (downy mildew) on various plants, eg P. cubensis on cucurbits or P. humili on hops; Pseudopezicula tracheiphila (red or rotbrenner disease, anamorph: Phialophora) CQQCnn / l 7Π7 / Β / ΥΙΛΙ in vines; Puccinia spp. (rusts) on various plants, e.g. P. triticina (leaf or brown rust), P. striiformis (stripe 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) triticirepentis (brown spot) on wheat or P. teres (net spot) on barley; Pyricularia spp., eg, P. oryzae (teleomorph: Magnaporthe grísea, rice fungus) on rice and P. grísea on turf and cereals; Pythium spp. (drop) on grass, rice, corn, wheat, cotton, rapeseed, sunflower, soybean, sugar beet, vegetables and various other plants (eg P. ultimum or P. aphanidermatum), Ramularia spp., eg R collo-cygni (Ramularia leaf spots, physiological leaf spots) on barley and R. beticola on sugar beets; Rhizoctonia spp. on cotton, rice, potato, grass, maize, rapeseed, potato, sugar beet, vegetables and various other plants, eg R. solani (root and stem rot) on soybean, R. solani (sheath blight) on rice or R. cerealis (Rhizoctonia spring blight) on wheat or barley; Rhizopus stolonifer (black mold, mild rot) on strawberries, carrots, cabbage, vines, and tomatoes; Rhynchosporium secalis (scald) on barley, rye, and triticale; Sarocladium oryzae and S. attenuatum (sheath rot) on rice; Sclerotinia spp. (stem rot or white mold) on vegetables and field crops such as rapeseed, sunflower (eg S. sclerotiorum) and soybean (eg S. rolfsii or S. sc / erotiorum); Septoria spp. on various plants, eg S. glycines CQQCnn / l 7Π7 / Β / ΥΙΛΙ (brown spot) on soybean, S. tritici (Septoria spot) on wheat and S. (syn. Stagonospora) nodorum (Stagonospora spot) on cereals; Uncinula (syn. Erysiphe) necator (powdery mildew, anamorphous: Oidium tuckeri) on vines; Setospaeria spp. (leaf blight) on corn (eg, S. turcicum, syn. Helminthosporium turcicum) and turf; Sphacelotheca spp. (smut) on corn, (eg, S. reiliana: top soot), sorghum, and sugarcane; Sphaerotheca fuliginea (powdery mildew) on cucurbits; Subterranean spongospora (powdery scab) on potatoes and thus transmitted viral diseases; Stagonospora spp. in cereals, eg S. nodorum Stagonospora, teleomorph: Leptosphaeria [syn. Phaeosphaeria] nodorum) on wheat; Synchytrium endobioticum on potato (potato wart disease); Taphrina spp., for example, T. deformaos (leaf roll disease) on peach and T. pruni (plum pitting) on ​​plums; Thielaviopsis spp. (black root rot) on tobacco, pome fruit, vegetables, soybeans, and cotton, eg, T. basicola (syn. Chalara elegans); Tilletia spp. (smut) 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., eg U. occulta (stem soot) on rye; Uromyces spp. (rust) on vegetables, such as beans (eg, U. appendiculatus, syn. U. phaseoli) and sugar beets (eg, U. betae); Ustilago spp. (loose soot) on cereals (eg, U. nuda and U. avaenae), corn (eg, U. maydis·. corn soot), and sugarcane; Venturia spp. (scab) on apples (eg, V. inaequalis) and pears; and Verticillium CQQCnn / l 7Π7 / Β / ΥΙΛΙ spp. (wilting) on ​​various plants, such as fruit and ornamentals, vines, soft fruit, vegetables, and field crops, eg, V. dahliae on strawberries, rapeseed, potatoes, and tomatoes. Preferred Mixtures and Combinations of Compounds Preferred mixtures and combinations of the carboxamide compound of Formula (I) with other active ingredients for soil application and seed treatment methods are described below. As mentioned above, in one embodiment of the invention, the pesticidal compound of Formula (I) can be combined and used in a mixture with at least one other agriculturally applied active compound II, such as another insecticidal active, an active fungicide or a biopesticide. In another embodiment of the invention, the pesticidal compound of the Formula (I) can be combined and used in a mixture with more than one additional active compound applied in agriculture. Thus, the pesticidal compound of Formula (I) can be combined and used in a mixture with more than one additional insecticide and / or with more than one fungicide. For example, the pesticidal compound of Formula (I) can be combined and used in a mixture with 1, 2, 3 or 4 additional agriculturally acceptable active compounds selected from fungicides and / or insecticides. Preferably, such additional compounds are active against soil-dwelling arthropod pests or phytopathogenic fungi. CQQCnn / l 7Π7 / Β / ΥΙΛΙ that inhabit the soil. One of the average level of the trade is familiar with such compounds and knows which compounds are active against a specific target organism. The following lists M of pesticides and F of fungicides, together with which the compounds according to the invention can be used and with which potential synergistic effects can occur, are intended to illustrate the possible combinations, but without imposing any limitation: The following M list of pesticides, grouped and numbered according to the Pesticide Resistance Action Committee (IRAC) Classification of Mode of Action, with which the compounds according to the invention may be used and with which potential synergistic effects may occur, it is intended to illustrate possible combinations, but without imposing any limitation: M.1 Acetylcholine esterase (AChE) inhibitors of the class of: M.1A carbamates, eg aldicarb, alanicarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur, thiodicar b, thiophanox, trimetacarb, XMC, xylylcarb and triazamate; or the class of M.1B Organophosphates, e.g. acetate, azamethifos, azinphos-ethyl, azinphosmethyl, cadusaphos, chlorethoxyphos, chlorfenvinphos, chlormephos, chlorpyrifos, chlorpyrifos-methyl, coumaphos, cyanophos, demeton-Smethyl, diazinon, dichlorvos / DDVP, dicrotof os, dimethoate, CQQCnn / l 7Π7 / Β / ΥΙΛΙ dimethylvinphos, disulfoton, EPN, ethion, ethoprofos, famfur, fenamifos, fenitrothion, fenthion, fostiazate, heptenofos, imiciafos, isofenphos, isopropyl O-(methoxyaminothio-phosphoryl) salicylate, isoxathion , malathion, mecarbam, methamidophos, metidathion, mevinphos, monocrotophos, naled, omethoate, oxydemeton-methyl, parathion, parathion-methyl, phenthoate, phorate, phosalone, phosmet, phosphamidon, phoxim, p¡r¡mifós-meti Io, profenofos, propetamphos, prothiophos, pyraclophos, pyridafenthion, quinalphos, sulfotep, tebupyrimfos, temephos, terbufos, tetrachlorvinphos, thiometon, triazophos, trichlorfon, and vamidothion; M.2. GABA-regulated chloride channel antagonists, for example: M.2A organochlorine cyclodiene compounds, eg endosulfan or chlordane; either M.2B fiproles (phenylpyrazoles), eg ethiprole, fipronil, flufiprole, pyrafluprole and pyrafluprole; M.3 Sodium channel modulators in a class of: M.3A pyrethroids, eg acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin, bifenthrin, bioallethrin, bioallethrin S-cyclopentenyl, bioresmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin , cypermethrin, alpha-cypermethrin, betacypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin, deltamethrin, empentrin, esfenvalerate, etofenprox, fenpropatrin, fenvalerate, flucitrinate, fIucitrinate, tau-fluvalinate, halfenprox, heptafluthrin, imiprothrin , meperfluthrin, metofluthrin, momfluorothrin, permethrin, phenothrin, prallethrin, profluthrin, pyrethrin (pyrethrum), CQQCnn / l 7Π7 / Β / ΥΙΛΙ resmethrin, silafluofen, tefluthrin, tetramethylfluthrin, tetramethrin, tralomethrin, and transfluthrin; either M.3B Sodium channel modulators, such as DDT or methoxychlor; M.4 Nicotinic acetylcholine receptor (nAChR) agonists of the class of: M.4A neonicotinoids, eg, acetamiprid, ch I o th i an i n i n, cycloxaprid, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam; or the compounds M.4 A. 2: (2E-)-1-[(6-chloropyridin-3-¡l)methyl]-N'-nitro-2-pentylidenehydrazinecarboximidamide; either M4.A.3: 1 - [(6-chloropyrid¡n-3-¡l)methyl]-7-methyl-8-n¡tro-5-propoxy¡-1,2,3 ,5,6,7hexahudroimidazo[1,2-a]pyridine; or of the nicotine class M.4B; M.5 Allosteric activators of the nicotinic acetylcholine receptor of the spinosyn class, eg, spinosad or spinetoram; M.6 Chloride channel activators of the class of avermectins and milbemycins, eg abamectin, emamectin benzoate, ivermectin, lepimectin or milbemectin; M.7 Juvenile hormone mimics, for example, M.7A juvenile hormone analogs, such as hydroprene, cynoprene, and methoprene; or others, such as M.7B phenoxycarb 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 CQQCnn / l 7Π7 / Β / ΥΙΛΙ emetic; Μ.9 Homeopteran selective feeding blockers, e.g. M.9B pymetrozine, or M.9C flonicamid; M.10 Mite growth inhibitors, eg M.10A clofentezine, hexythiazox and diflovidazin, or M.10B etoxazole; M.11 Microbial disruptors of insect midgut membranes, eg 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 Inhibitors of mitochondrial ATP synthase, e.g. M.12A diafenthiuron, or M.12B organotin acaricides, such as azocyclotin, cyhexatin or phenbutatin oxide, or M.12C propargite, or M.12D tetradifon; M.13 Uncouplers of oxidative phosphorylation by altering the proton gradient, eg chlorfenapyr, DNOC or sulframid; M.14 Nicotinic acetylcholine receptor (nAChR) channel blockers, eg nereistoxin analogues such as bensultap, cartap hydrochloride, thiocyclam or thiosultap sodium; M.15 Type 0 chitin biosynthesis inhibitors, such as benzoylureas, eg bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, CQQCnn / l 7Π7 / Β / Υ noviflumuron, teflubenzuron, or triflumuron; M.16 Chitin biosynthesis type 1 inhibitors, eg buprofezin; M.17 Molt disruptors, Diptera, eg, cyromazine; M.18 Ecdysone receptor agonists, such as diacylhydrazines, eg methoxyfenozide, tebufenozide, halofenozide, fufenozide or chromafenozide; M.19 Octopamine receptor agonists, eg amitraz; M.20 Inhibitors of mitochondrial complex III electron transport, e.g. M.20A hydramethylnon, M.20B acequinocyl or M.20C fluacrypyrim; M.21 Inhibitors of electron transport of mitochondrial complex I, e.g. M.21A METI insecticides and acaricides, such as fenazaquin, fenpyroximate, pyrimidifene, pyridaben, tebufenpyrad or tolfenpyrad, or M.21B rotenone; M.22 Voltage-gated sodium channel blockers, eg, M.22A indoxacarb or M.22B metaflumizone or M.22B.1: 2-[2-(4-cyanophenyl)1 -[3-(trifluoromethyl)phenyl]et¡l¡den]-N-[ 4-(d¡fluoromethox¡)phenyl]h¡drazincarboxamide or M.22B.2: N-(3-chloro-2-methylphenyl)-2-[(4clorotenyl)[4-[ methyl(methylsulfon 11)amino]phenyl]methylene]hydrazinecarboxamide; M.23 Acetyl CoA carboxylase inhibitors, such as tetronic and tetramic acid derivatives, e.g. spirodiclofen, spiromesifen or CQQCnn / l 7Π7 / Β / ΥΙΛΙ spirotetramate; Μ.24 Inhibitors of mitochondrial complex IV electron transport, e.g. M.24A phosphine, such as aluminum phosphide, calcium phosphide, zinc phosphine or phosphide, or M.24B cyanide; M.25 Inhibitors of mitochondrial complex II electron transport, such as beta-ketonitrile derivatives, eg cyenopyraphen or cyflumethophen; M.28 Ryanodine receptor modulators of the diamide class, e.g. flubendiamide, chlorantranil iprol (rynaxypyr®), c i ant ran i I ip ro I (cyazypyr®) or the phthalamide compounds M.28.1: (R)-3-chloro-N1-{2-methyl-4-[1,2,2,2-tetraf I uor-1 (trifluoromethyl)ethyl]phenyl}-N2-( 1-methyl 1-2-methylsulfo ni letyl)phthal amide and M.28.2: (S)-3-chloro-N1-{2-methyl-4-[1,2,2,2-tetrafluoro-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 -cycloprop¡let¡l)carbamo¡l]phenyl}1 -(3-chlorpyridin-2-¡l )-1H-pyrazole-5-carboxamide (proposed ISO name: cyclaniliproI), or the compound M.28.4: methyl-2-[3,5-d¡bromo-2-({[3-bromo-1 -(3-chlorpyrid¡n-2-¡l)-1 Hpyrazol-5-yl]carbon¡ l}am¡no)benzo¡l]-1,2-dimethylhydrazinecarboxylate; or a compound selected from M.28.5a) to M.28.5I): M.28.5a) N-[4,6-dichloro-2-[(d¡et¡l-lambda-4-sulfan¡l¡den)carbamo¡l]-fen¡l]2-(3-chloro- 2-pyridl)-5-(trifluoromethyl)pyrazole-3-carboxamide; M.28.5b) N-[4-chloro-2-[(diet¡l-lambda-4-sulfan¡l¡den)carbamo¡l]-6-methyl CQQCnn / l 7Π7 / Β / ΥΙΛΙ fen iI]-2-(3-clo ro-2-pi r¡d¡ I)-5-(trif I uo ro met¡ I)p¡ razo I-3-carboxam ¡ gives; M.28.5c) N-[4-chloro-2-[(di-2-propyl-lambda-4-sulfan¡l¡den)carbamo¡l]-6methyl l-phen i l]-2-(3-chloro -2-pyrid¡l)-5-(trifluoromethyl)p¡ razo I-3-carboxam ida; M.28.5d) N-[4,6-dichloro-2-[(d¡-2-prop¡l-lambda-4-sulfanyl¡dene)carbamo¡l]phenyl]-2-(3-chloro-2 -pyridyl)-5-(trifluoromethyl I)p i razo I-3-carboxamide; M.28.5e) N-[4,6-dichloro-2-[(d¡et¡l-lambda-4-sulfan¡l¡den)carbamoyl]-phenyl]2-(3-chloro-2- pyridyl)-5-(difluoromethyl)pyrazole-3-carboxamide; M.28.5f) N-[4,6-dibromo-2-[(d¡-2-prop¡l-lambda-4-sulfanyl¡dene)carbamo¡l]phenyl]-2-(3-chloro-2 -pyridyl)-5-(trifluoromethyl I )pi razo I-3-carboxam ida; M.28.5g) N-[4-chloro-2-[(di-2-propyl-lambda-4-sulfan¡l¡den)carbamo¡l]-6-cyano-phenyl]-2-(3-chloro -2-p¡r¡d¡l)-5-(trifluoromethyl)p¡razol-3-carboxamide; M.28.5h) N-[4,6-dibromo-2-[(d¡et¡l-lambda-4-sulfanil¡dene)carbamo¡l]phenyl]-2-(3-chloro-2-pyrid¡ l)-5-(trifluoromethyl)pyrazo I-3-carboxamide ida; M.28.5Í) N-[2-(5-amino-1,3,4-thiadiazol-2-¡l)-4-chloro-6-methylphenyl]-3-bromo1 - (3 -chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide; M.28.5j) 3-chloro-1 - (3-chloro-2-pyridinyl)-N-[2,4-dichloro-6-[[(1-cyano-1-methylethyl)amino]carbon l]phenyl]-1H-pyrazole-5-carboxamide; M.28.5k) 3-bromo-N-[2,4-dichloro-6-(methylcarbamol)phenyl]-1 -(3,5-dichloro-2pyrid i I)-1 H-pyrazole- 5-carboxamide; M.28.5I) N-[4-chloro-2-[[(1,1-dimethylethyl)amino]carbonyl]-6-methylphenyl]-1-(3chloro-2-pyridinyl)-3-(fluoromethoxy)-1 H-pyrazole-5-carboxamide; or a compound selected from M.28.6: N-(2-cyanopropan-2-¡l)-N-(2,4-dimethylphenyl)-3-iodobenzene-1,2-dicarboxamide; either M.28.7: 3-chloro-N-(2-cyanopropan-2-¡l)-N-(2,4-dimethylphenyl)-benzene-1,2 CQQCnn / l 7Π7 / Β / ΥΙΛΙ dicarboxamide; Μ. 28.8a) 1-(3-chloro-2-pyridinyl)-N-[4-cyano-2-methyl-6[(m ethylamino )carbon i l]f en i I ]-3-[[5- (t ri f I uo ro m et i I) - 2 H-tetrazo I-2 - i I] m eti I] - H-pyrazole-5-carboxamide; either M.28.8b) 1-(3-chloro-2-pyridinyl)-N-[4-cyano-2-methyl-6[(methylamino)carbonyl]phenyl]-3-[[5-(tr ¡fluoromethyl)-1H-tetrazol-1-yl]methyl]1H-pyrazole-5-carboxamide; M.A. Insecticidal active compounds with unknown or uncertain mode of action, e.g. afoxolaner, azadirachtin, amidoflumet, benzoximate, biphenazate, bromopropylate, quinomethionate, cryolite, dicofol, flufenerim, flometoquin, fluensulfone, fluopyram, flupyradifurone, fluralaner, methoxadiazone, piperonyl butoxide, piflubumide, pyridalyl, pyrifluquinazone, sulfoxaflor, thioxazaphen, triflumezopyrim, or the compounds M.A. 3: 11 -(4-chloro-2,6-dimethylphenyl)-1-2-hydroxy-1,4-dioxa-9azadispiro[4.2.4.2]-tetradec-11-en-10-one, or the compound M.A. 4: 3-(4'-fluoro-2,4-dimethyllb¡phenyl-3-¡l)-4-hydroxy¡-8-oxa-1azaspiro[4.5]dec-3-en-2-one, or the compound M.A. 5: 1-[2-fluoro-4-methyl-5-[(2,2,2-trifluoroethyl)sulfinyl]phenyl]-3(trifIuoromethyl)-1H-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-p¡rid¡l)met¡l]-2-p¡r¡d¡l¡den]-2 ,2,2-trifluoroacetamide; CQQCnn / l 7Π7 / Β / ΥΙΛΙ M.UN.6b) (E / Z)-N-[1-[(6-chloro-5-fluoro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-acetamide; M.UN.6C) (E / Z)-2,2,2-trifluoro-N-[1-[(6-fluoro-3-pyridyl)methyl]-2-pyridylidene]acetamide; M.UN.6d) (E / Z)-N-[1-[(6-bromo-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-acetamide; M.UN.6e) (E / Z)-N-[1-[1-(6-chloro-3-pyridyl)ethyl]-2-pyridylidene]-2,2,2-trifluoroacetamide; M.UN.6Í) (E / Z)-N-[1 -[(6-chloro-3-p¡r¡d¡l)met¡l]-2-pyr¡d¡l¡den]-2 ,2-difluoroacetamide; M.UN.6g) (E / Z)-2-chloro-N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2-difluoro-acetamide; M.UN.6h) (E / Z)-N-[1-[(2-chloropyr¡m¡din-5-¡l)methyl]-2-pyrid¡l¡den]-2,2, 2-trifluoro-acetamide; M.UN.6Í) (E / Z)-N-[1-[(6-chloro-3-p¡rid¡l)met¡l]-2-p¡r¡d¡l¡den]-2 ,2,3,3,3pentaflu oro-pro pan amide·); M.UN.6j) N-[1 - [(6-chloro-3-pyr¡d¡l)methyl]-2-p¡r¡d¡l¡den]-2,2,2-tr fluorothioacetamide or the compound M.UN.6k) N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-N'isopropyl-acetamidine or the compounds M.UN.8: 8-chloro-N-[2-chloro-5-methox¡feml)sulfonyl]-6-tr¡fluoromethyl)imidazo[1,2-a]pyr¡d¡n-2- carboxamide; either M.UN.9: 4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-¡l]-2-methylN-(1 -oxothietan-3-yl)benzamide; either CQQCnn / l 7Π7 / Β / ΥΙΛΙ M.UN.1 0: 5-[3-[2,6-dichloro-4-(3,3-d¡chloroal¡loxy)phenox¡]propoxy¡]-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-(benzoylmethylam¡no)-N-[2-bromo-4-[1,2,2,3,3,3-hexafluoro1 -(trifluoromethyl)propyl ]-6-(trifluoromethyl)phenyl]-2-fluoro-benzamide; M.UN.11 .c) 3-(benzoylmethylamino)-2-fluoro-N-[2-iodo-4-[1,2,2,2tetrafluoro-1 - (trifluoromethyl)ethyl] -6-(trifluoromethyl)phenyl]-benzamide; M.UN.11 .d) N-[3-[[[2-iodo-4-[1,2,2,2-tetraf I or gold -1 -(tr if I or gold meti I) eti I ] -6(t¡fluoromethyl)phenyl]am¡no]carbonyl]phenyl]-N-methyl-benzam¡de; M.UN.11 .e) N-[3-[[[2-bromo-4-[1,2,2,2-tetrafluoro-1 -(trifluoromethyl)ethyl]-6(trifluoromethyl)phen ¡l]amino]carbon¡l]-2-fluorophenyl]-4-fluoro-N-methylbenzamide; M.UN.11 .f) 4-fluoro-N-[2-fluoro-3-[[[2-iodo-4-[1, 2,2,2-tetraf fluoro-1 (trifluoromethyl) et¡ l]-6-(t¡fluoromethyl)phenyl]am¡no]carbon¡l]phenyl]-N-methylbenzamide; M.UN.11 .g) 3-fluoro-N-[2-fluoro-3-[[[2-iodo-4-[1,2,2,2-tetrafluoro-1 (trifluoromethyl)et¡l ]-6-(t¡fluoromethyl)phenyl]am¡no]carbon¡l]phenyl]-N-methylbenzamide; M.UN.11 .h) 2-chloro-N-[3-[[[2-iodo-4-[1,2,2,2-tetrafluoro-1(trifluoromethyl)ethyl]-6-(trifluorometh ¡l)phenyl]amino]carbonyl]phenyl]-3-pyridinecarboxamide; M.UN.11.i) 4-cyano-N-[2-cyano-5-[[2,6-dibromo-4-[1,2,2,3,3,3-hexafluoro1 -(trifluorometh ¡l)prop¡l]phenyl]carbamo¡l]phenyl]-2-methyl-benzamide; M.UN.11 .j) 4-cyano-3-[(4-cyano-2-methyl-benzo¡l)am¡no]-N-[2,6-dichloro-4[1, 2,2,3,3,3-hexafluoro-1-(trifluoromethyl)propyl]phenyl]-2-fluoro-benzamide; CQQCnn / l 7Π7 / Β / ΥΙΛΙ M.UN.11 .k) N-[5-[[2-chloro-6-cyano-4-[1,2,2,3,3,3-hexafluoro-1(trifluoromethyl)prop¡ l]phenyl]carbamol]-2-cyano-phenyl]-4-cyano-2-methylbenzamide; M.UN.11.1) N-[5-[[2-bromo-6-chloro-4-[2,2,2-trifluoro-1-hydroxy-1(trifluoromethyl)ethyl]phenyl] carbamo¡l]-2-cyano-phenyl]-4-cyano-2-methylbenzamide; M.UN.11 .m) N-[5-[[2-bromo-6-chloro-4-[1,2,2,3,3,3-hexafluoro-1(trifluoromethyl)propyl] phenyl]carbamol]-2-cyano-phenyl]-4-cyano-2-methylbenzamide; M.UN.11 .n) 4-cyano-N-[2-cyano-5-[[2,6-dichloro-4-[1,2,2,3,3,3-hexafluoro1 -(trifluoromethyl )prop¡l]fen¡l]carbamo¡l]fen¡l]-2-methyl-benzamide; M.UN.11 .o) 4-cyano-N-[2-cyano-5-[[2,6-dichloro-4-[1,2,2,2-tetrafluoro-1 (trifluorometh¡ l)ethyl]phen¡l]carbamo¡l]fen¡l]-2-methyl-benzam¡de; M.UN.11 .p) N-[5-[[2-bromo-6-chloro-4-[1,2,2,2-tetrafluoro-1 (trifluoromethyl)et¡l]phenyl] carbamol]-2-cyano-phenyl]-4-cyano-2-methylbenzamide; 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.1 2.a) 2-(1,3-d¡oxan-2-¡l)-6-[2-(3-pyr¡d¡n¡l)-5-t¡azol¡l ]-pyridine; M.A.12. b) 2-[6-[2-(5-f I uo ro-3-pi r i di n i I)-5-thiazo I i l]-2-pyrid in i I]-pyri mid i n a; M.UN.12.c) 2-[6-[2-(3-pyridinyl)-5-thiazolyl]-2-pyridinyl]-pyrimidine; M.UN.1 2.d) N-methylsulfon¡l-6-[2-(3-p¡r¡d¡l)thiazol-5-yl]p¡r¡d¡n-2-carboxam gives M.UN.12.e) N-methylsulfonyl-6-[2-(3-p¡r¡dyl)thiazol-5-¡l]p¡r¡d¡n-2-carboxam¡de M.UN.1 2. f) N-ethyl-N-[4-methyl-2-(3-p¡r¡d¡l)t¡azol-5-¡l]-3-methylt¡opropanamide CQQCnn / l 7Π7 / Β / ΥΙΛΙ M.UN.1 2. g) N-methyl-N-[4-methyl-2-(3-p¡r¡d¡l)t¡azol-5-¡l]-3-methylt¡opropanamide M.UN.1 2. h) N,2-dimethyl-N-[4-methyl-2-(3-p¡r¡d¡l)t¡azol-5-¡l]-3-meth opropanamide M.A.12. i) N-ethyl-2-methyl-N-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-3-methylthiopropanamide M.A.12. j) N - [4-cl gold-2 - (3-p¡ r id i I) thi azo I-5-i I] - N-et i I-2 - met i I-3 - met i 11 i or propanamide M.UN.1 2. k) N-[4-chloro-2-(3-pyrid¡l)thiazol-5-¡l]-N,2-d¡methyl-3-methylt¡opropanamide M.UN.1 2.1) N-[4-chloro - 2-(3-p i r id i I) th i azo I-5-i I] - N - m et i I-3 - m et i I thi o propanamide M.UN.1 2. m) N-[4-chloro-2-(3-pyridyl)t¡zol-5-¡l]-N-ethyl-3-methylt¡opropanamide; or the compound M.UN.13: 2-(4-methoxy i mi nocid hexy 1)-2-(3,3,3trif I u or ro prop i I s u If o n i I) acetone nitrile; or the compounds M.UN.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]pyridine -5-ol; or the compound M.UN.15: 1-[(2-chloro-1,3-thiazol-5-¡l)methyl]-3-(3,5-d¡clorofeníl)-9-methyl-4oxo-4H- pyrido[1,2-a]pyrimidin-1-io-2-olate. M.Y Biopesticides, which are pesticide compounds of biological origin with insecticidal, acaricidal, molluscidal and / or CQQCnn / l 7Π7 / Β / ΥΙΛΙ nematicide, which includes M.Y-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, (Clariva®, P. reneformis, P. usagae, Pseudomonas fluorescens, Steinernema feltiae, Streptomces galbus; or active based on bacillus firmus (Votivo®, 1-1582), or M.Y-2 Biochemical pesticides: L-carvone, citral , (E,Z)-7,9-dodecadien-1 -yl acetate, ethyl formate, (E,Z)-2,4-ethyl decadienoate ( pear), (Z,Z,E)-7,11,13hexadecatrienal, heptyl butyrate, isopropyl myristate, lavadulyl senecioate, 2-methyl 1-butanol, methyl eugenol, methyl jasmonate, (E,Z)-2 ,13octadecadien-1-ol, (E,Z)-2,13-octadecadien-1-ol acetate, (E,Z)-3,13-octadecadien-1-ol, R-1 -octen-3-ol, 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-11CQQCnn / l 7Π7 / Β / Υ tetradecen-1 -ol-, black locust extract, grapefruit seeds and pulp, extract of Chenopodium ambrosiodae, catnip oil, neem oil, quillaia extract, tagetes oil, or components of the ginkgo tree selected from the group consisting of bilobalide, ginkgolide A, ginkgolide B, ginkgolide C, ginkgolide J and ginkgolide M. Combinations of the carboxamide compound of Formula (I) with one or more insecticidally active compounds selected from the group consisting of acetate, chlorpyrifos, fipronil are preferred. methiocarb, thiodicarb, lamba-cyhalothrin, bifenthrin, cypermethrin, alphacypermethrin, tefluthrin, acetamiprid, clothianidin, dinotefuran, imidacloprid, thiacloprid, abamectin, emamectin, flubendiamine, spinosad, triflumezopyrim, chlorantraniliprole, or cyantraniliprole. More preferred is the combination of the carboxamide compound of the Formula (I) with acetate. It is more preferred, the combination of the compound of CQQCnn / l 7Π7 / Β / ΥΙΛΙ carboxamide of Formula (I) with chlorpyrifos. More preferred is the combination of the carboxamide compound of Formula (I) with fipronil. More preferred is the combination of the carboxamide compound of Formula (I) with methiocarb. More preferred is the combination of the carboxamide compound of Formula (I) with thiodicarb. Most preferably, the combination of the carboxamide compound of Formula (I) with Es of most preferred, carboxamide of Formula (I) with Es of most preferred, carboxamide of Formula (I) with Es of most preferred, carboxamide of Formula (I) with more preferred Es, carboxamide of Formula (I) with more preferred Es, carboxamide of Formula (I) with more preferred Es, carboxamide of Formula (I) with more preferred Es , carboxamide of Formula (I) with more preferred Es, carboxamide of Formula (I) with more preferred Es, carboxamide of Formula (I) with more preferred Es, carboxamide of Formula (I) with Es of most preferably, carboxamide of Formula (I) cypermethrin. the combination of bifenthrin compound. the combination of the tefluthrin compound. the combination of alpha-cypermethrin compound. the combination of the abamectin compound. the combination of the emamectin compound. the combination of the spinosad compound. the combination of the sulfoxaflor compound. the combination of triflumezopyrim compound. the combination of the compound chlorantraniliprole. the compound combination of ci an tran i I ip ro I. the combination of the compound with N-[4,6-dichloro-2-[(diethyl-lambda-4CQQCnn / l 7Π7 / Β / ΥΙΛΙ sulfan¡lidene)carbamo¡l]-fen¡l]-2-(3- chloro-2-p¡r¡d¡l)-5-(trifluoromethyl)p¡razole 3-carboxamide. More preferably, the combination of the carboxamide compound of the Formula (I) with N-[4-chloro-2-[(diethyl-lambda-4-sulfanylidene)carbamoyl]-6-methyl-phenyl]-2-(3-chloro-2-pyridyl)-5(trifluoromethyl)pi razol-3-carboxamide. More preferred is the combination of the carboxamide compound of Formula (I) with N-[4-chloro-2-[(di-2-propyl-lambda-4-sulfanylidene)carbamoyl]-6-methyl-phenyl]-2 -(3-chloro-2-pyridyl)-5(trifluoromethyl)pyrazole-3-carboxamide. Combinations of the carboxamide compound of Formula (I) with neonicotinic compounds of group M.4 are preferred. Most preferred is the combination of the carboxamide compound of Formula (I) with acetamiprid. Also most preferred is the combination of the carboxamide compound of the Formula (I) with clothianidin. of of of of It is also carboxamide of the It is also carboxamide of the It is also carboxamide of the It is also carboxamide of the Most preferably, the combination Formula (I) with dinotefuran. highest preference, the combination Formula (I) with imidacloprid. highest preference, the combination Formula (I) with thiacloprid. highest preference, the combination Formula (I) with thiamethoxam. preferably, the combination of the of the of the of the compound compound compound compound compound of CQQCnn / l 7Π7 / Β / ΥΙΛΙ carboxamide of Formula (I) with active ingredients depending on bacillus firmus (Votivo, bacillus firmus strain 1-1582). Most preferred is the combination of the carboxamide compound of Formula (I) with PONCHO® / VOT¡VO™. Most preferred is the combination of the carboxamide compound of Formula (I) with an active from P. nishizawae (Clariva®). The commercially available compounds of group M listed above can be found in The Pesticide Manual, 15th Edition, C.D.S. Tomlin, British Crop Protection Council (2011), among other publications. The neonicotinoid cycloxaprid is known from WO20120 / 069266 and WO201 1 / 06946, and the neonicotinoid compound M.4A.2, sometimes also called guadipir, is known from WO2013 / 003977, and the neonicotinoid compound M.4A.3. (approved as paichongding in China) is known from WO201 0 / 069266. The metaflumizone analogue M.22B.1 is described in CN 10171577, and the analogue M.22B.2 in CN102126994. Both M.28.1 and M.28.2 phthalamides are known from WO 2007 / 101540. Anthranilamide M.28.3 was described in WO2005 / 077934. The hydrazide compound M 28.4 was described in WO 2007 / 043677. The anthranilamides M.28.5a) to M.28.5h) can be prepared as described in WO 2007 / 006670, WO201 3 / 024009 and WO201 3 / 024010, the anthranilamide compound M.28.5Í) is described in WO201 1 / 085575, compound M.28.5j) in WO2008 / 134969, compound M.28.5k) in US201 1 / 0461 86 and compound M.28.5I) in WO201 2 / 034403. The diamide compounds M.28.6 and M.28.7 can be found at CN102613183. The anthranilamide compounds M.28.8a) and M.28.8b) are known from WO201 0 / 069502. The quinoline derivative flometoquin is shown in CQQCnn / l 7Π7 / Β / ΥΙΛΙ WO2006 / 013896. The aminofuranone flupyradifurone compounds are known from WO 2007 / 1 15644. The sulfoximine compound sulfoxaflor is known from WO2007 / 149134. From the group of pyrethroids, momfluorothrin is known from US6908945 and heptafluthrin from WO10133098. The oxadiazolone compound, methoxadiazone can be found in JP13 / 166707. The acaricidal pyrazole piflubumide is known from WO2007 / 020986. Isoxazoline compounds were described in the following publications: fluralaner in WO2005 / 08521 6, afoxolaner in WO2009 / 002809 and in WO201 1 / 149749, and the isoxazoline compound M.UN.9 in WO2013 / 050317. The pyripyropene derivative afidopiropen was described in WO 2006 / 129714. Nematicidal thioxazaphene was described in WO09023721 and nematicidal fluopyram in WO2008126922, nematicidal mixtures comprise flupyram in WO201 01 0861 6. Triflumezopyrim compound was described in WO201 2 / 0921 1 5. The spiroketal-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 1. Triazoylphenylsulfide M.UN.5 was described in WO2006 / 043635, and the bacillus firmus-based biological control agents in WO2009 / 1 24707. The compounds M.UN.6a) to M.UN.6Í) listed in M.UN.6 were described in WO2012 / 029672, and the compounds M.UN.6j) and M.UN.6k) in WO201 31 29688. The nematicidal compound M.UN.8 in WO201 3 / 055584, and the pyridalyl-like analogue M.UN.10 in WO2010 / 060379. The carboxamide compounds M.UN.H.b) to M.UN.11.h) can be prepared as described in WO 2010 / 018714 and the carboxamide M.UN.11Í) to M.UN.11.p) CQQCnn / l 7Π7 / Β / ΥΙΛΙ as described in WO201 0 / 1 27926. The p¡ridiItiazoles 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) WO2012000896, and M.UN.12.f) to M.UN.12.m) of WO2010129497. The malononitrile compound M.UN.13 was described in WO2009 / 0051 10. The compounds M.UN.14a) and M.UN.14b) are known from WO2007 / 101369. The compound M.UN.15 can be found in WO13192035. Biopesticides from the M.Y. they are described below in the paragraphs on biopesticides (from groups M.Y and F.XII). The following list F of fungicidally active substances, together with which the compounds according to the invention can also be used, is intended to illustrate the possible combinations, but does not limit them: F.l) Respiration inhibitors F.l 1) Complex III inhibitors at the Qo site (for example, strobilurins): azoxystrobin, coumethoxystrobin, coumoxystrobin, dimoxystrobin, enestroburin, fenaminstrobin, phenoxystrobin / fluphenoxystrobin, fluoxastrobin, cresoxim-methyl, mandestrobin, metominostrobin, orysastrobin, picoxystrobin n, pyraclostrobin, pyramethostrobin, pyroxystrobin, triphIoxystrobin and 2-(2-(3(2,6-dichlorophenyl)-1-methyl-allyldenam¡nooxmethyl)-phenyl)-2-methox¡¡m¡ noN-methyl-acetamide, pyribencarb, triclopyricarb / chlorodincarb, famoxadone, fenamidone; F.l 2) Inhibitors of complex III at the Q¡ site: ciazofamid, amisulbrom, [(3S,6S,7R,8R)-8-benzyl-3-[(3-acetoxy-4-methoxy¡pyr¡) 2-methylpropanoate d¡n-2-carbon¡l)am¡no]-6-methyl-4,9-dioxo-1,5-dioxonan-7-yl], CQQCnn / l 7Π7 / Β / ΥΙΛΙ [(3S,6S,7R,8R)-8-benzyl-3-[[3-(acetox¡methoxy¡)-4methoxy¡-p¡r¡d¡n-2-carbonyl]am¡no 2-methylpropanoate [(3S,6S,7R,8R)-8-benzyl-3-[(3- isobutoxy¡carbonyloxy¡-4methoxy-pyridine-2-carbonyl)amino]-6-methyl-4,9-dioxo-1,5-dioxonan-7-yl], [(3S,6S,7R,8R) 2-methylpropanoate -8-benzyl-3-[[3-(1,3-benzodioxol-5¡lmethoxy¡)-4-methoxy-p¡r¡d¡n-2-carbon¡l]am¡no]-6-meth ¡l-4,9-dioxo-1,5dioxonan-7-yl]; [(3S,6S,7R,8R)-8-benzyl-3-[[3-(1,3benzod¡oxol-5-ylmethoxy¡)-4-methoxy¡-p¡r¡d¡n 2-methylpropanoate -2-carbon¡l]am¡no]-6-methyl-4,9dioxo-1,5-dioxonan-7-yl]; (3S,6S,7R,8R)-3-[[(3h¡droxy-4-methoxy-2-p¡r¡d¡nyl)carbon¡l]am¡no]-6-meth¡ 2-methylpropanoate l-4,9-d¡oxo-8(phenylmethyl)-l ,5-dioxonan-7-yl F.l 3) Complex II inhibitors (for example, carboxamides): benodanil, benzovindiflupyr, bixaphen, boscalid, carboxin, fenfuram, fluopyram, flutolanil, fluxapyroxad, furametpyr, isofetamid, isopyrazam, mepronil, oxycarboxin, penflufen, penthiopyrad, sedaxane, tecloftalam, thifluzamide, N(4'-trifluoro methylthiob¡phenyl-2-yl)-3-d¡fluorometh¡ 1-1-methyl-1H-pyrazole-4carboxamide, N-(2-(1,3, 3-trimethyl-butyl)-phenyl)-1,3-dimethyl-5-fluoro-1Hpyrazole-4-carboxamide, 3-(difluoromethyl)-1-methyl-N-(1,1, 3-trimethylindan-411)pyrazole-4-carboxamide, 3-(trifluoromethyl)-1-methyl-N-(1,1,3-trimethylindan4-11)pyrazole-4-carboxamide, 1,3- dimethyl-N-(1,1,3-1 r i m et i I i nd an-4-i I) p¡ raz o I 4-carboxamide, 3-(trifluoromethyl)-1,5-dimethyl-N-(1 ,1,3-trimethyllindan-4yl)pyrazole-4-carboxamide, 1,3,5 -1 r i m et i I - N - (1,1,3-trimethyllindan-4-yl)p¡razol4 -carboxamide, N-(7-fluoro-1,1,3-trimethyl-indan-4-yl)-1,3-dimethyl-pyrazole-4-carboxamide, N-[2-(2,4-dichlorophenyl)- 2-methoxy-1-methyl-ethyl]-3(difluoromethyl)-1-methyl-pyrazoI-4-carboxamide; N-[2-(2,4 CQQCnn / l 7Π7 / Β / ΥΙΛΙ difluorofen¡l)fen¡l]-3-(tr¡fluorometh¡l)pyraz¡n-2-carboxam¡da; F.l 4) Other respiration inhibitors (for example, complex I, uncouplers): diflumetorim, (5,8-difIuoroquinazoIin-4-iI)-{2-[2-fIuoro4-(4-trifluoromethylp¡r¡d ¡n-2-¡lox¡)-fen¡l]-et¡l}-am¡na; nitrophenyl derivatives: binapacryl, dinobuton, dinocap, fluazinam; ferimzone; organometal compounds: fentin salts, such as fentin acetate, fentin chloride or fentin hydroxide; ametoctradin; and silthiopham; F.ll) Sterol biosynthesis inhibitors (SBI fungicides) F.ll 1) C14 demethylase inhibitors (DMI fungicides): triazoles: azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, oxpoconazole, paclobutrazol, penconazole, propiconazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole, uniconazole, 1-[rel-(2S;3R)-3-(2-chlorophenyl)-2-(2, 4d i f I u o rof en i I)-oxiran i I m eti I] - 5-thi ocyanato -1 H-[1,2,4]triazo 1, 2-[rel-(2S;3R) -3(2-chlorophenyl)-2-(2,4-d¡fluorophenyl)-oxiran¡lmethyl]-2H-[1,2,4]triazol-3-thiol, 2[2- chloro-4-(4-chlorophenoxy)phenyl]-1-(1,2,4-triazol-1-yl)pentan-2-ol, 1-[4-(4chlorophenoxy)-2-(trifluoromethyl)phen ¡l]-1 -cyclopropi 1-2-(1,2,4-triazol-1 i I) ethane 1,2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1 ,2,4-triazol-1-yl)butan-2-ol, 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1,2,4-triazol-1-yl)butan-2-ol , 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-3-methyl-1-(1,2,4-triazol-1yl)butan-2-ol , 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triazo I1 -yl)propan-2-ol, 2-[2-chloro-4-( 4-chlorophenoxy)phenyl]-3-methyl-1 -(1,2,4-triazol1-yl)butan-2-ol, 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phen¡ l]-1 - (1,2,4 CQQCnn / l 7Π7 / Β / ΥΙΛΙ triazol-1 - yl)pentan-2-ol, 2-[4-(4-fluorophenoxy)-2-(t¡fluoromethyl)fen¡l]-1 (1,2 ,4-triazol-1-yl)propan-2-ol; imidazoles: imazalil, pefurazoate, prochloraz, triflumizole; pyrimidines, pyridines and piperazines: fenarimol, nuarimol, pyrifenox, triforine, [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 facetate, fenpropimorph, tridemorph, fenpropidin, piperalin, spiroxamine; F.ll 3) 3-keto reductase inhibitors: fenhexamid; F.111) Nucleic acid synthesis inhibitors F.lll 1) Acylamino acid or phenylamide fungicides: benalaxil, benalaxilM, kiralaxil, metalaxil, metalaxil-M (mefenoxam), ofurace, oxadixil; F.lll 2) Others: himexazole, octilinone, oxolinic acid, bupirimate, 5-fluorocytosine, 5-fluoro-2-(p-tol¡lmethoxy)pyrimidin-4-amine, 5-fluoro-2-(4fluorofen¡ lmethoxy)pyrimidin-4-amine; F.IV) Inhibitors of cell division and cytoskeleton F.IV 1) Tubulin inhibitors, such as benzimidazoles, thiophanates: benomyl, carbendazim, fuberidazole, thiabendazole, thiophanate-methyl; triazolopyrimidines: 5-chloro-7-(4-methylpiper¡din-1-¡l)-6-(2,4,6trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine dyne; F.IV 2) Other inhibitors of cell division: dietofencarb, ethaboxam, pencicuron, fluopicolid, zoxamid, metrafenon, pyriophenon; F.V) Amino acid and protein synthesis inhibitors F.V 1) Methionine synthesis inhibitors (ani I i n o-pyrimidines): cyprodinil, mepanipyrim, pyrimethanil; F.V 2) Protein synthesis inhibitors: blasticidin-S, kasugamicin, CQQCnn / l 7Π7 / Β / ΥΙΛΙ kasugamicin hydrochloride-hydrate, 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: quinoxyfen; F.VII) Inhibitors of lipid and membrane synthesis F.VII 1) Phospholipid biosynthesis inhibitors: edifenfos, iprobenfos, pyrazofos, isoprothiolane; F.VII 2) Lipid peroxidation: dichloran, quintocene, technazene, toclofos-methyl, biphenyl, cloroneb, etridiazole; F.VII 3) Phospholipid biosynthesis and cell wall deposition: dimethomorph, flumorph, mandipropamid, pirimorf, bentiavalicarb, iprovalicarb, valifenalate and (4-f I uorof en i I) acid ester N-(1-( 1-(4-cyanophenyl)ethanesulfonyl)-but-2-yl)carbamic; F.VII 4) Compounds that affect the permeability of the cell membrane and fatty acids: propamocarb, propamocarb-hydrochloride F.VII 5) Fatty acid amide hydrolase inhibitors: oxathiapiproline; 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) Tio- and dithiocarbamates: ferbam, mancozeb, maneb, metam, metiram, propineb, tiram, zineb, ziram; F.VIII 3) Organochlorine compounds (for example: phthalimides, sulfonamides, CQQCnn / l 7Π7 / Β / ΥΙΛΙ chloronitriles): anilazine, el o rotal o ni I, captafol, captan, folpet, d el of I u an id, dichlorophen, hexachlorobenzene, pentachlorophenol and its salts, phthalide, tolifluanid, N-( 4-chloro-2-n¡tro-phenyl)-N-ethyl-4-methyl-benzenesulfonamide; F.VIII 4) Guanidines and others: guanidine, dodine, dodine free base, guazatin, guazatin-acetate, iminoctadine, iminoctadine-triacetate, im¡noctad¡na-tris(albes¡late), dithianon, 2,6-dimethyl -1H,5H-[1,4]dithiino[2,3c:5,6-c']dipyrrole-1,3,5,7(2H,6H)-tetraone; F.IX) Cell wall synthesis inhibitors F.IX 1) Glucan synthesis inhibitors: validamycin, polyoxin B; F.IX-2) Melanin synthesis inhibitors: pyroquilon, tricyclazole, carpropamide, dicyclomet, fenoxanil; F.X) Plant defense inducers F.X 1) Acibenzolar-S-methyl, probenazole, isothianil, thiadinyl, prohexadionacalcium; F.X 2) Phosphonates: fosetyl, fosetyl-aluminium, phosphoric acid and its salts, 4-cycloprop¡l-N-(2,4-dimethoxy¡fen¡l) t¡ad¡azole-5-carboxamide; F.XI) Mode of action unknown: bronopol, quinomethionate, cyflufenamid, cymoxanil, dazomet, debacarb, diclomezine, difenzoquat, difenzoquat-methylsulfate, diphenylamine, fenpyrazamine, flumetover, flusulfamide, flutianil, metasulfocarb, nitrapyrin, nitrotal-isopropyl, oxathiapiproline, picarbutrazox, tolprocarb , 2[3,5- bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-(prop-2-yn-1yloxy)phenyl]-4,5-dihydro -1,2-oxazol-3-yl}-1,3-thazol-2-yl)piperidin-1 yl]ethanone, 2-[3,5-bis(difluoromethyl)-1 H- pyrazol-1-yl]-1-[4-(4-{5-[2-fluoro-6(prop-2-yn-1-yloxy)phenyl]-4,5-d¡hydro- 1,2-oxazol-3-yl}-1,3-thiazol-2CQQCnn / l 7Π7 / Β / ΥΙΛΙ ¡l)piperid¡n-1-yl]ethanone, 2-[3,5-bis(d¡fluoromethyl )-1H-pyrazol-1-yl]-1-[4-(4{5-[2-chloro-6-(prop-2-yn-1-yloxy)phenyl]-4,5-dihydro-1 ,2-oxazol-3-yl}-1,3thiazol-2-yl)piperidin-1-yl]ethanone, oxina-copper, proquinazid, tebufloquin, tecloftalam, triazoxide, 2-butoxy-6-iodo-3-prop¡ lchromen-4-one, N(cyclopropylmethoxyim¡no-(6-difluoro-methoxy-2,3-d¡fluoro-phenyl)-methyl)-2phenylacetamide, N'-(4-( 4-chloro-3-t¡fluoromethyl-phenox¡)-2,5-dimethyl-phenyl)-Netyl-N-methylformamidine, N'-(4-(4-fluoro-3-trifluoromethyl- fenox¡)-2,5dimet¡l-fen¡l)-N-et¡l-N-met¡lformamid¡na, N'-(2-met¡ l-5-trifluoro meti 1-4-(3tr¡met¡ ls¡lan¡l-propoxy¡)-phenyl)-N-ethyl-N-methylformamid¡na, Ν'-(5-trifluoromethyl-2-methyl-4-(3-trimethylsilanyl-propoxy)-phenyl )-N-ethyl-N-methylformamidine, methoxy-acetic acid 6-tert-butyl-8-fluoro-2,3-dimethyl-quinolin-4-yl ester, 3-[5-(4-methylphenyl)-2,3- dimethyl-isoxazolidin-3-yl]pyridine, 3-[5-(4-cl o ro-phen i I)-2,3-d¡ methy I-i soxazo I i di n-3-i I]-p¡ r id i n a (pyrisoxazole), N-(6-methoxy-pyridin-3¡l)cyclopropanecarboxylic acid amide, 5-chloro-1-(4,6-dimethoxy-pyrimidin-2-yl)- 2-methyl1H-benzoimidazole, 2-(4-chloro-phenyl)-N-[4-(3,4-d¡meth¡ox¡-phenyl)-¡soxazol-5yl]-2- ethyl prop-2-yn¡lox¡-acetamide, (Z)-3-amino-2-cyano-3-phenyl-prop-2-enoate, N-[6-[[(Z Pentyl )-[(1-methyltetrazol-5-yl)-phenyl-methylene]amino]oxymethyl]-2-pyridyl]carbamate, 2-[2-[(7,8-difluoro-2-meth ¡l-3-quinol¡l)ox¡]-6fluoro-phenyl]propan-2-ol, 2-[2-fluoro-6-[(8-fluoro-2-methyl-3-quinol¡ l)ox¡]phenyl]propan-2-ol, 3-(5-fluoro-3,3,4,4-tetramethyl-3,4-d¡h¡d¡dro¡soqu¡nol¡n-1 ¡l) quinoline, 3-(4,4-d¡fluoro-3,3-dimethyl-3,4-d¡hdro¡soquinol¡n-1yl)quinoline, 3-(4,4,5- trifluoro-3,3-dimethyl-3,4-d¡d¡droisoqu¡nolin-1 ¡l)quinoline; F.XII) Biopesticides F.XII 1) Microbial pesticides with fungicidal, bactericidal, antiviral and / or activating plant defense activity: Ampelomyces quisqualis, Aspergillus flavus, Aureobasidium pullulans, Bacillus amyloliquefaciens, B. mojavensis, B. pumilus, B. simplex, B sol i salt yes, B. subtilis, B. subtilis var. amyloliquefaciens, Candida oleophila, C. saitoana, Clavibacter michiganensis (bacteriophages), Coniothyrium minitans, Cryphonectria parasitica, Cryptococcus albidus, Dilophosphora 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 chlo raphis, Pseudozyma flocculosa, Pichia anomalous, Pythium oligandrum, Sphaerodes mycoparasitica, Streptomyces griseoviridis, S. lydicus, S. violaceusniger, Talaromyces flavus, Trichoderma asperellum, T. atroviride, T. fertile, T. gamsii, T. harmatum; T. harzianum, a mixture of T. harzianum and T. viride; mixture of T. polysporum and T. harzianum; T. stromaticum, T. virens (also called Gliocladium virens), T. viride, Typhula phacorrhiza, Ulocladium oudemansii, Verticillium dahlia, zucchini yellow mosaic virus (antiviral strain); F.XII 2) Biochemical pesticides with fungicidal, bactericidal, antiviral and / or activating plant defense activity: chitosan (hydrolyzed), hairpin protein, laminarin, menhaden fish oil, natamycin, pox virus coat protein from the CQQCnn / l 7Π7 / Β / ΥΙΛΙ plum, potassium or sodium bicarbonate, Reynoutria sachlinensis extract, salicylic acid, tea tree oil; Preferably, the fungicide is selected from Amisulbrom, Azoxystrobin, Benalaxyl, Benzovindiflupyr, Bixaphen, Boscalid, Coumethoxystrobin, Coumoxystrobin, Cyazofamid, Cyproconazole, Difenoconazole, Dimethomorph, Dimoxystrobin, Etaboxam, Fludioxonil, Fluopyram, Fluoxastrobin, Fluquincon azole, fluxapyroxad, himexazole, ipconazole, iprodione , isopyrazam, metalaxyl, metconazole, penflufen, pentiopyrad, Picarbutrazox, picoxystrobin, prochloraz, prothioconazole, pyraclostrobin, pyrimethanil, sedaxane, silthiopham, tebuconazole, thiabendazole, thiophanate methyl, thiram, Triadimenol, triazoxide, triflox istrobin, triticonazole, N-[2 -(2,4difluorophenyl)phenyl]-3-(trifluoromethyl)p¡raz¡n-2-carboxamide and 4-cyclopropylN-(2,4-dimethoxyphenyl)thiadiazole-5 -carboxamida. More preferably, the fungicide is selected from Amisulbrom, Azoxystrobin, Benzovindiflupyr, Boscalid, Difenoconazole, Dimethomorph, Fludioxonil, Fluopyram, Fluxapyroxad, Ipconazole, Metalaxyl, Penflufen, Penthiopyrad, Picarbutrazox, Picoxystrobin, Prothioconazole, Pyraclostrobin, Pyrimethanil, Sedaxane , silthiofam, thiophanate methyl, trifloxystrobin, triticonazole. Also preferred is the combination of the carboxamide compound of Formula (I) with a fungicide selected from the group consisting of 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1(1,2,4-triazole -1 yl)pentan-2-ol, 1-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1 cyclopropyl-2(1,2,4-triazol-1 - i I )ethanol, 2-[4-(4-chlorophenoxy)-2-(trifluorometh-yl)phenyl]-1(1,2,4-triazol-1-yl)butan-2-ol, 2-[ 2-chloro-4-(4-chlorophenoxy)phenyl]-1 -(1,2,4triazol-1 -yl)butan-2-ol, 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl ]-3-methylCQQCnn / l 7Π7 / Β / ΥΙΛΙ - (1,2,4-triazol-1 -yl)butan-2-ol, 2-[4-(4-chlorophenoxy¡)-2(trifluoromethyl)-iphenyl]-1-(1,2,4-tr iaz ol -1 - i I) propan - 2-o 1, 2-[2-chloro-4-(4chlorophenoxy)phenyl]-3-methyl-1-(1,2,4-triazol-1-yl )butan-2-ol, 2-[4-(4cloroten oxy)-2-(trifluoromethyl)-,f en i I] -1 -(1,2,4-triazol-1-yl)pentan-2- ol or 2[4-(4-fluorophenoxy)-2-(trifluoromethyl)-iphenyl]-1-(1,2,4-triazol-1-yl)propan-2-ol. Most preferred is the combination of the carboxamide compound of Formula (I) with 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1,2,4-triazoI-1-yl)pentan- 2-ol. Most preferably, the combination of the carboxamide compound of Formula (I) with 1-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-cyclopropyl-2-(1,2 ,4-triazol-1 -i I )ethanol Most preferably, the combination of the carboxamide compound of Formula (I) with 2-[4-(4-chlorophenoxy¡)-2-(trifluorometh-,¡l)phenyl]-1-(1,2 ,4-triazol-1 - i I) butan-2-ol Most preferably, the combination of the carboxamide compound of Formula (I) with 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1 -(1,2,4-triazoI-1 i I) bu tan-2-ο I Most preferred is the combination of the carboxamide compound of Formula (I) with 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-3-methyl-1(1,2,4-tr iazol-1-yl)butan-2-ol. Most preferred is the combination of the carboxamide compound of Formula (I) with 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)->phenyl]-1 -(1,2,4-triazol-1- i I) propan-2-o I. Most preferably, the combination of the carboxamide compound CQQCnn / l 7Π7 / Β / ΥΙΛΙ of Formula (I) with 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-3-methyl-1-(1,2,4triazol-1 - i I) bu tan-2-ol. Most preferably, the combination of the carboxamide compound of Formula (I) with 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)-'phenyl]-1-(1,2, 4-triazol-1-yl)pentan-2-ol. Most preferably, the combination of the carboxamide compound of Formula (I) with 2-[4-(4-fluorophenoxy)-2-(trifluoromethyl)->phenyl]-1 (1,2,4 -triazol-1-yl)propan-2-ol. Most preferred is the combination of the carboxamide compound of Formula (I) with azoxystrobin. Also most preferred is the combination of the carboxamide compound of Formula (I) with Boscalid. Also most preferred is the combination of the carboxamide compound of Formula (I) with Difenoconazole. Also most preferred is the combination of the carboxamide compound of Formula (I) with FludioxoniL Also most preferred is the combination of the carboxamide compound of Formula (I) with fluxapyroxad. Also most preferred is the combination of the carboxamide compound of Formula (I) with ipconazole. Also most preferred is the combination of the carboxamide compound of Formula (I) with epoxiconazole. Also most preferred is the combination of the carboxamide compound of Formula (I) with metalaxyl. Also most preferred is the combination of the compound of CQQCnn / l 7Π7 / Β / ΥΙΛΙ carboxamide of Formula (I) with penflufen. Also most preferred is the combination of the compound of CQQCnn / l 7Π7 / Β / ΥΙΛΙ carboxamide of Formula (I) with pyraclostrobin. Also most preferred is the combination of the carboxamide compound of Formula (I) with pyrimethanil. Also most preferred is the combination of the carboxamide compound of Formula (I) with sedaxane. Also most preferred is the combination of the carboxamide compound of Formula (I) with silthiopham. Also most preferred is the combination of the carboxamide compound of Formula (I) with thiophanate-Methyl. Also most preferred is the combination of the carboxamide compound of Formula (I) with triticonazole. Fungicide pesticides of a chemical nature described by common names, their preparation and their activity against pests are known (cf.: http: / / www.alanwood.net / pesticides / ); often these pesticides are commercially available. The fungicidal pesticides I described by the IUPAC nomenclature, their preparation and their pesticidal activity are also known (cf. Can. J. Plant Sci. 48(6), 587-94, 1968; EP-A 141 31 7; EP-A 1 52 031; 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; WO 01 / 54501 ; WO 01 / 56358; WO 02 / 22583; WO 02 / 40431 ; WO 03 / 10149; WO 1 / 03 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, WO 2012 / 168188, WO 2007 / 006670, WO 1 1 / 77514; WO 13 / 047749, WO 10 / 069882, WO 13 / 047441, WO 03 / 16303, WO 09 / 90181, WO 13 / 007767, WO 13 / 010862, WO 13 / 024009 and WO 13 / 024010). biopesticides Biopesticides of the II.M.Y or F.XII groups, their preparation and their pesticidal activity, for example against fungi or harmful 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 link A to Z). Biopesticides from group II.M.Y or F.XII. They can also have insecticidal, fungicidal, acaricidal, molluscidal, antiviral, bactericidal, pheromone, nematicidal, plant defense activating, plant stress reducing, plant growth regulating, plant growth promoting, plant growth regulator and / or performance enhancer. Many of these biopesticides are registered and / or commercially available: aluminum silicate (Screen™ Duo from Certis LLC, USA). CQQCnn / l 7Π7 / Β / ΥΙΛΙ USA), Agrobacterium radiobacter K1026 (eg NoGall® from Becker Underwood Pty Ltd., Australia), A. radiobacter K84 (Nature 280, 697-699, 1979; eg GalITroll® from AG Biochem, Inc., C , USA), Ampelomyces quisqualis M-10 (for example, AQ 10® from Intrachem Bio GmbH & Co. KG, Germany), extract or filtrate of Ascophyllum nodosum (Norwegian seaweed, brown seaweed) (for example, ORKA GOLD from Becker Underwood, South Africa; or Goemar® from Laboratoires Goemar, France), Aspergillus flavus NRRL 21882 isolated from peanuts 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, blastospores in BlossomProtect® from bio-ferm GmbH, Germany), Azospirillum brasilense XOH (for example, AZOS from Xtreme Gardening, USA or RTI Reforestation Technologies International; USA). USA), Bacillus amyloliquefaciens FZB42 (for example in RhizoVital® 42 from AbiTEP GmbH, Berlin, Germany), B. amyloliquefaciens IN937a (J. Microbiol. Biotechnol. 17(2), 280-286, 2007; eg, in BioYield® from Gustafson LLC, TX, USA), B. amyloliquefaciens IT-45 (CNCM I--3800) (eg, Rhizocell C from ITHEC, France), B. amyloliquefaciens subsp. plantarum MBI600 (NRRL B-50595, deposited with USDA (eg Integral®, Subtilex® NG from Becker Underwood, USA), 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® by Bayer Crop Science LP, USA), B. pumilus GB34 (ATCC 700814; e.g., in YieldShield® from Gustafson LLC, TX, USA) and Bacillus pumilus KFP9F CQQCnn / l 7Π7 / Β / ΥΙΛΙ (NRRL B-50754) (eg in Becker Underwood South Africa's BAC-UP or FUSION-P), B. pumilus QST 2808 (NRRL B--30087) (eg Sonata® and Bailad® Plus from AgraQuest Inc., USA, Ull.), B. subtilis GB03 (for example, Kodiak® or BioYield® from Gustafson, Inc., USA; or Companion® from Growth Products, Ltd., White Plains, NY 10603, USA), B. subtilis GB07 (Epic® by Gustafson, Inc., USA), B. subtilis QST-713 (NRRL B--21661 on Rhapsody®, Serenade® MAX and Serenade® ASO from AgraQuest Inc., USA), B. subtilis var. amyloliquefaciens FZB24 (eg Taegro® from Novozyme Biologicals, Inc., USA), B. subtilis var. amyloliquefaciens D747 (eg Double Nickel 55 from Certis LLC, USA), B. thuringiensis ssp. aizawai ABTS-1 857 (for example, from XenTari® from BioFa AG, Münsingen, Germany), B. t. ssp. aizawai SAN 401 I, ABG6305 and ABG-6346, Bacillus t. ssp. israelensis AM65-52 (eg, in VectoBac® from Valent BioSciences, IL, USA), Bacillus thuringiensis ssp. kurstaki SB4 (NRRL B-50753; eg, Beta Pro® from Becker Underwood, South Africa), B. t. ssp. kurstaki ABTS-351 identical to HD-1 (ATOO SD-1275; eg, in Dipel® DF from Valent BioSciences, IL, USA), B. t. ssp. kurstaki EG 2348 (for example, from Lepinox® or Rapax® from CBC (Europe) S.r.L, 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 called SAN 418 I or ABG-6479; previous production strain from Novo-Nordisk), B. t. ssp. tenebrionis NB-176 (or NB-176-1) a gamma-irradiated induced high-yield mutant of strain NB-125 (DSM 5480; EP 585 215 B1; Novodor® from Valent BioSciences, Switzerland), Beauveria bassiana ATOO CQQCnn / l 7Π7 / Β / ΥΙΛΙ 74040 (for example, from Naturalis® by CBC (Europe) S.r.L, Italy), B. bassiana DSM 12256 (US 200020031495; for example, BioExpert® SC by Uve Systems Technology S.A., Colombia), B. bassiana GHA (BotaniGard® 22WGP from Laverlam Int. Corp., USA), B. bassiana PPRI 5339 (ARSEF number 5339 in the USDA Agricultural Research Service (ARS) Collection of Entomopathogenic Fungal Cultures; NRRL 50757) (e.g., BroadBand® from Becker Underwood, South Africa), B. brongniartii (for example, in Agrifutur's Melocont®, Agrianello, Italy, for the control of the San Juan beetle; J. Appl. Microbiol. 100(5),1063-72, 2006), Bradyrhizobium sp . (eg, Vault® from Becker Underwood, USA), B. japonicum (eg, VAULT® from Becker Underwood, USA), Candida oleophila 1-182 (NRRL Y-18846; eg, 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 (by example, Biocure® (in admixture with lysozyme) and BioCoat® from Micro Fio Company, USA (BASF SE) and Arysta), chitosan (eg ArmourZen® from BotriZen Ltd., NZ), Clonostachys rosea f. catenulata, also called Gliocladium catenulatum (for example, isolate J 1446: Prestop® from Verdera Oy, Finland), Chromobacterium subtsugae PRAA41 isolated from soil on an eastern spruce (Tsuga canadensis) in the Catoctin Mountain region of central Maryland (for example, in GRANDEVO from Marrone Bio Innovations, USA), Coniothyrium mínitans CON / M / 91-08 (for example, Contans® WG from Prophyta, Germany), Cryphonectria parasitica (for example, Endothia parasitica from CNICM, France) , Cryptococcus albidus (for example, YIELD PLUS® from Anchor CQQCnn / l 7Π7 / Β / ΥΙΛΙ Bio-Technologies, South Africa), Cryptophlebia leucotreta granulovirus (CrleGV) (eg in CRYPTEX from Adermatt Biocontrol, Switzerland), Cydia pomonella granulovirus (CpGV) V03 (DSM GV-0006; eg in MADEX Max from Andermatt Biocontrol, Switzerland ), CpGV V22 (DSM GV0014; eg in MADEX Twin from Adermatt Biocontrol, Switzerland), Delftia acidovorans RAY209 (ATCC PTA-4249; WO 2003 / 57861; eg in BIOBOOST from Brett Young, Winnipeg, Canada), Dilophosphora alopecuri (Lidophia graminis from Becker Underwood, Australia), Ecklonia maxima (seaweed) extract (eg KELPAK SL from Kelp Products Ltd, South Africa), Formononetin (eg in MYCONATE from Plant Health Care pie, UK), Fusarium oxysporum (for example, BIOFOX® from S.I.A.P.A., Italy, FUSACLEAN® from Natural Plant Protection, France), Glomus intraradices (for example, MYC 4000 from ITHEC, France), Glomus intraradices RTI-801 (for example, MYKOS from Xtreme Gardening, USA or RTI Reforestation Technologies International; USA), extract of grapefruit seeds and pulp (for example, BC-1000 from Chemie S.A., Chile), hairpin (alpha-beta) protein (for example, MESSENGER or HARP-NTek from Plant Health Care Pie, UK; Science 257, 1-132, 1992), Heterorhabditis bacteriophaga (for example Nemasys® G from Becker Underwood Ltd., UK), Isaria fumosorosea Apopka-97 (ATCC 20874) (PFR-97™ from Certis LLC, USA). ), cis-jasmone (US 8,221,736), laminarin (for example, from 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 Verticillium lecanii) (for example, CQQCnn / l 7Π7 / Β / ΥΙΛΙ 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, 107-115; Biological Control 31(2), 145-154, 2004), Metarhizium anisopliae var. acridum IMI 330189 (isolate from Ornithacris cavroisi in Niger; also NRRL 50758) (eg GREEN MUSCLE® from Becker Underwood, South Africa), M. a. var. acridum FI-985 (eg GREEN GUARD® SC from Becker Underwood Pty Ltd, Australia), M. anisopliae Fl1045 (eg BIOCANE® from Becker Underwood Pty Ltd, Australia), M. anisopliae F52 (DSM 3884, ATCC 90448 eg MET52® Novozymes Biologicals BioAg Group, Canada), M. anisopliae ICIPE 69 (eg METATHRIPOL from ICIPE, Nairobe, Kenya), Metschnikowia fructicola (NRRL Y-30752; eg SHEMER® from Agrogreen, Israel, now distributed by Bayer CropSciences, Germany; US 6,994,849), Microdochium dimerum (for example, ANTIBOT® from Agrauxine, France), Microsphaeropsis ochracea P130A (ATCC 74412 isolated from apple leaves of an abandoned apple 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 (for example, in Muscudor™ development products or QRD300 from AgraQuest, USA), neem oil (for example, TRILOGY®, TRIACT®70 EC from Certis LLC, USA), Nomuraea rileyi strains SA861 01, GU87401, SR86151, CG128 and VA9101, Paecilomyces fumosoroseus FE 9901 ( eg NO FLY™ from Natural Industries, Inc., USA), P. lilacinus 251 (eg in BioAct® / MeloCon® from Prophyta, Germany; CQQCnn / l 7Π7 / Β / ΥΙΛΙ Crop Protection 27, 352-361, 2008; originally isolated from infected nematode eggs in the Philippines), P. lilacinus DSM 15169 (eg, NEMATA® SO from Uve Systems Technology S.A., Colombia), P. lilacinus BCP2 (NRRL 50756; eg, PL GOLD from Becker Underwood BioAg SA Ltd, South Africa), mixture of Paenibacillus alvei NAS6G6 (NRRL B50755), 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 / 801 69), Penicillium bilaiae (eg, Jump Start® from Novozymes Biologicals BioAg Group, Canada, originally isolated from soil in southern Alberta; Fertilizer Res. 39, 97-103, 1994) , Phlebiopsis gigantea (eg RotStop® from Verdera Oy, Finland), Pichia anomala WRL076 (NRRL Y-30842; US 8,206,972), potassium bicarbonate (eg, Amicarb® from Stáhler SA, Switzerland), potassium silicate (eg, SilMATRIX™ from Certis LLC, USA), Pseudozyma flocculosa PF-A22 UL (eg, Sporodex® from Plant Products Co. Ltd., Canada), Pseudomonas sp. DSM 13134 (WO 2001 / 40441, eg in PRORADIX by Sourcon Padena GmbH & Co. KG, Hechinger Str. 262, 72072 Tübingen, Germany), P. chloraphis MA 342 (for example in CERALL or CEDEMON by BioAgri AB, Uppsala, Sweden), P. fluorescens CL 145A (for example, in ZEQUANOX from Marrone Biolnnovations, Davis, CA, CQQCnn / l 7Π7 / Β / ΥΙΛΙ USA; J. Invertebr. Pathol. 1 13(1):104-14, 2013), Pythium oligandrum DV 74 (ATCC 38472; eg POLYVERSUM® from Remeslo SSRO, Biopreparaty, Czech Republic and GOWAN, USA; US 2013 / 0035230), extract from Reynoutria sachlinensis (eg REGALIA® SC from Marrone Biolnnovations, Davis, CA, USA), Rhizobium leguminosarum bv. phaseolii (eg RHIZO-STICK from Becker Underwood, USA), R. I. trifolii RP113-7 (eg DORMAL from Becker Underwood, USA; AppL Environ. Microbiol. 44(5), 1096-1 101), R.I.bv. viciae P1NP3Cst (also called 1435; New Phytol 179(1), 224-235, 2008; for example, in NODULATOR PL Peat Granule from Becker Underwood, USA; or in NODULATOR XL PL from Becker Underwood, Canada), R. I. bv. viciae SU303 (eg NODULAID Group E from Becker Underwood, Australia), R.I. bv. viciae WSM1455 (eg 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 called strain 2011 or RCR2011 (Mol Gen Genomics (2004) 272: 1-17; eg 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 (for example, MILLENIUM® from Becker Underwood Ltd., UK), S. feltiae (NEMASHIELD® from BioWorks, Inc., USA; NEMASYS® from Becker Underwood Ltd., UK. ), S. krausseí L137 (NEMASYS® L from Becker Underwood Ltd., UK), Streptomyces griseoviridis K61 (for example, MYCOSTOP® from Verdera Oy, Espoo, Finland; Crop Protection 25, 468-475, 2006), S. lydicus WYEC 108 (for CQQCnn / l 7Π7 / Β / ΥΙΛΙ example, Actinovate® from Natural Industries, Inc., USA, US 5,403,584), S. violaceusniger YCED-9 (for example, DT-9® from Natural Industries, Inc. , USA, US 5,968,503), Talaromyces flavus V117b (for example, PROTUS® from Prophyta, Germany), Trichoderma asperellum SKT-1 (for example, ECO-HOPE® from Kumiai Chemical Industry Co., Ltd., Japan), T. asperellum ICC 012 (eg, in TENET WP, REMDIER WP, BIOTEN WP from Isagro NC, USA, BIO-TAM from AgraQuest, USA), T. atroviride LC52 (eg, SENTINEL® from Agrimm Technologies Ltd, NZ), T. atroviride CNCM 1-1237 (eg from Esquive WG from Agrauxine S.A., France, eg against pruning lesion diseases on vines and plant root pathogens ), T. fertile JM41R (NRRL 50759; eg, RICHPLUS™ from Becker Underwood Bio Ag SA Ltd, South Africa), T. gamsii ICC 080 (eg, from TENET WP, REMDIER WP, BIOTEN WP from Isagro NC, USA). USA, BIO-TAM from AgraQuest, USA), T. harzianum T-22 (eg, PLANTSHIELD® from Firma BioWorks Inc., USA), T. harzianum TH 35 (eg, ROOT PRO ® from Mycontrol Ltd., Israel), T. harzianum T-39 (for example, TRICHODEX® and TRICHODERMA 2000® from Mycontrol Ltd., Israel and Makhteshim Ltd., Israel), T. harzianum and T. viride (for example, TRICHOPEL from Agrimm Technologies Ltd, NZ), T. harzianum ICC012 and T. viride ICC080 (eg REMEDIER® WP from Isagro Ricerca, Italy), T. polysporum and T. harzianum (eg BINAB® from BINAB Bio-lnnovation AB, Sweden), T. stromaticum (for example, TRICOVAB® from C.E.P.L.A.C., Brazil), T. virens GL-21 (also called Gliocladium virens) (for example, SOILGARD® from Certis LLC, USA), T. viride (for example, TRIECO® from CQQCnn / l 7Π7 / Ε / ΥΙΛΙ Ecosense Labs. (India) Pvt. Ltd., India, BIO-CURE® F from T. Stanes & Co. Ltd., India), T. viride TV1 (for example, T. viride TV1 from Agribiotec srl, Italy) and Ulocladium oudemansii HRU3 (eg in BOTRY-ZEN® from Botry-Zen Ltd, NZ). Strains may originate from genetic resources and repository centers: American Type Culture Collection, 10801 University Blvd., Manassas, VA 201 10-2209, USA (strains with ATCC prefix); CABI Europe - International Mycological Institute, Bakeham Lane, Egham, Surrey, TW20 9TYNRRL, R. LL (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 CBS prefix); Division of Plant Industry, CSIRO, Canberra, Australia (strains with the prefix CC); Collection Nationale de Cultures de Microorganismes, Instituí Pasteur, 25 rue du Docteur Roux, F-75724 PARIS Cedex 15 (strains with the prefix CNCM); Leibniz-Institut DSMZDeutsche Sammlung von Mikroorganismen und Zellkulturen GmbH, InhoffenstraBe 7 B, 38124 Braunschweig, Germany (strains with DSM prefix); International Depositary Authority of Cañada Collection, Canada (strains with IDAC prefix); International Collection of Micro-orgniasms 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 UTA prefix); The National Collections of Industrial and Marine Bacteria Ltd., Torry Research Station, P.O. Box 31, 135 Abbey Road, Aberdeen, AB9 8DG, Scotland (strains with the NCIMB prefix); ARS Culture Collection of the National Center for CQQCnn / l 7Π7 / Β / ΥΙΛΙ Agricultural Utilization Research, Agricultural Research Service, United States Department of Agriculture, 1815 North University Street, Peoria, Illinois 61604, USA (strains prefixed with NRRL); Department of Scientific and Industrial Research Culture Collection, Applied Biochemistry Division, Palmerston North, New Zealand (strains with the NZP prefix); FEPAGRO-Fundagáo Estadual de Pesquisa Agropecuária, Rúa Gongalves Dias, 570, Bairro Menino Deus, Porto Alegre / RS, Brazil (strains with the prefix SEMIA); SARDI, Adelaide, South Australia (strains with the SRDI prefix); 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 (USDA strains prefix: Beltsville Rhizobium Culture Collection Catalog, March 1987 USDAARS ARS-30: http: / / pdf.usaid.gov / pdf_docs / PNAAW891.pdf); and Murdoch University, Perth, Western Australia (strains with the WSM prefix). Other strains can be found in the world catalog of microorganisms: http: / / gcm.wfcc.info / and http: / / www.landcareresearch.co.nz / resources / collections / icmp and other references to collections of strains 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 under the strain designation Bacillus subtilis 1430 (and is identical to NCIMB 1237). MBI 600 was recently reclassified as Bacillus amyloliquefaciens subsp. plantarum based on a polyphasic test CQQCnn / l 7Π7 / Β / ΥΙΛΙ which combines classical microbiological methods using a mix of traditional tools (such as culture-based methods) and molecular tools (such as fatty acid analysis and genotyping). Thus, Bacillus subtilis MBI600 (or MBI 600 or MBI600) is identical to Bacillus amyloliquefaciens subsp. plantarum MBI600, formerly Bacillus subtilis MBI600. Bacillus amiloliquefaciens MBI600 is known as a plant growth promoting seed treatment for rice from Int. J. Microbiol. Res. 3(2) (2011), 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 the roots of red beets in North America (System Appl. Microbiol 27 (2004) 372-379). This B. subtilis strain promotes plant health (US 2010 / 0260735 A1; WO 201 1 / 109395 A2). B. subtilis FB17 was also deposited with ATCC under the number PTA-1 1857 on April 26, 2011. Bacillus subtilis strain FB17 may 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-219 (NRRL B-50619) , B. amyloliquefaciens AP-295 (NRRL B-50620), B. japonicum SEMIA 5079 (for example, Gelfix 5 or Adhere 60 from Nitral Urbana Laoboratories, Brazil, a BASF company), B. japonicum SEMIA 5080 (for example, GELFIX CQQCnn / l 7Π7 / Β / ΥΙΛΙ or ADHERE 60 from Nitral Urbana Laoboratories, Brazil, a BASF company), B. mojavensis AP-209 (NRRL B-50616), B. solisalsi AP-21 7 (NRRL B-50617) , B. pumilus strain INR-7 (also called BU-F22 (NRRL B50153) and BU-F33 (NRRL B-50185)), B. simplex ABU 288 (NRRL B-50340), and B. amyloliquefaciens subsp. plantarum MBI600 (NRRL B-50595) were mentioned, inter alia, 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, diethylethanolammonium jasmonate, methyl ester jasmonic acid, jasmonic acid amide, jasmonic acid methylamide, jasmonic acid-L-amino acid (amide-linked) conjugates (for example, conjugated with Lysoleucine, L-valine, L-leucine, or L-phenylalanine), 12-acid oxophytodienoic acid, coronatin, coronaphacoyl-L-serine, coronaphacoyl-L-threonine, 1-oxo-indanoyl-isoleucine methyl esters, 1-oxo-indanoilleucine methyl esters, coronalon (2-[(6-ethyl-l-oxo -indan-4-carbonyl)amino]-3-methyl-pentanoic), linoleic acid or derivatives thereof, and cisjasmone, or combinations of any of the foregoing. Humates are humic and fulvic acids that are mined from a form of lignite coal and clay, known as leonardite. Humic acids are organic acids that occur in humus and other organically derived materials, such as peat and certain CQQCnn / l 7Π7 / Β / ΥΙΛΙ soft coals. It was shown that they increase the efficiency of the fertilizer with respect to the uptake of phosphate and micronutrients by the plants and contribute to the development of the root systems of the plants. 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-d¡h¡droxid¡h¡dro-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 have also been previously described and reported: 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 by methods known in the state of the 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 of bilobalide (in enantiopure form), ginkgolide A (in its racemic form) and ginkgolide B (in its racemic form) can be obtained by chemical synthesis, as is described, for example, in Tetrahedron Letters (1988), 29(28), 3423-6, Tetrahedron Letters (1988), 29(26), 32056 and Journal of the American Chemical Society (2000), 122(35), 8453-8463, respectively. Examples of mixtures Examples of some mixtures according to the present invention are described in the tables below. The agriculturally acceptable Active Component II, with which the compound of Formula I can be combined, is an insecticide or a fungicide as identified and abbreviated according to the codes listed in Table B. CQQCnn / l 7Π7 / Β / ΥΙΛΙ Table B Component II Apr. Component II Apr. 5 Azoxystrobin I l-F-1 Thiabendazole I l-F-21 T r if I oxystrobin I l-F-2 Ipconazole I l-F-22 Picoxystrobin I l-F-3 Tebuconazole I l-F-23 Pyraclostrobin I l-F-4 T riadimenol I l-F-24 Sedaxane I 1-F-5 Prochloraz I 1-F-25 10 Penthiopyrad I 1-F-6 Fluquinconazole I 1-F-26 Penflufen I 1-F-7 Triticonazole I 1-F-27 Fluopyram I 1-F-8 Fl u di ox i n i I I 1-F-28 Fluxapyroxad I 1-F-9 Carboxin I 1-F-29 Boscalid ll-F-1 0 Siltiofam I 1-F-30 15 Oxathiapiprolin I 1-F-11 Ziram I 1-F-31 Metalaxil ll-F-1 2 Thiram I 1-F-32 Metalaxil -M ll-F-1 3 Carbendazim I 1-F -33 Etaboxam ll-F-1 4 Thiophanate methyl I l-F-34 20 Dimethomorph ll-F-1 5 Fipronil 11-1-1 Valifenalate ll-F-1 6 CI oti anidin II-I-2 Cyproconazole ll- F-1 7 Thiamethoxam II-I-3 Difenoconazole II-F-1 8 Acetamiprid II-I-4 Prothioconazole II-F-1 9 Dinotefuran II-I-5 Flutriafol I I-F-20 Imidacloprid II-I-6 Component II Apr. Thiacloprid 11-1-7 Sulfoxaflor 11-1-8 Methiocarb 11-1-9 T Efluthrin 11-1-1 0 Bifenthrin 11-1-1 1 Cypermethrin 11-1-1 2 alpha-cypermethrin II-1-1 3 Spinosad II-1-1 4 C i antran i I ip ro I 11-1-1 5 Component II Apr. C lo rantran i I i prol 11-1-16 Thiodicarb 11-1-1 7 T riflumezopyrim (mesoionic) 11-1-1 8 acetate 11-1-1 9 C lo rp i ri fo s II-I-20 flupyradifurone 11-1-21 Abamectin II-I-22 CQQCnn / l 7Π7 / Β / ΥΙΛΙ In some embodiments, the present invention relates to mixtures comprising the compound of Formula (I) and at least one additional agriculturally acceptable active component II, such as an insecticide or fungicide from Table B. Thus, the mixtures comprise a compound of Formula (I) and an additional agriculturally acceptable active ingredient II from Table B. Therefore, in the context of the present invention, each of the rows in Table B-1 corresponds to a mixture of Compound I (of Formula (I)) to be applied in the methods according to the present invention. Table B-1 Mix No. Comp. 1 comp. II M.B1.1 1 1 l-F-1 M.B1.2 1 I l-F-2 M.B1.3 1 I l-F-3 M.B1.4 1 I l-F-4 M.B1.5 1 I l-F- 5 M.B1.6 1 I l-F-6 M.B1.7 1 I l-F-7 M.B1.8 1 I l-F-8 M.B1.9 1 I l-F-9 M.B1.10 1 I l-F- 1 0 M.B1.11 1 Il-F-11 M.B1.12 1 ll-F-1 2 M.B1.13 1 Il-F-1 3 M.B1.14 1 Il-F-1 4 M.B1. 15 1 ll-F-1 5 M.B1.16 1 ll-F-1 6 M.B1.17 1 ll-F-1 7 M.B1.18 1 ll-F-1 8 M.B1.19 1 ll-F-1 9 M.B1.20 1 Il-F-20 M.B1.21 1 Il-F-21 M.B1.22 1 Il-F-22 M.B1.23 1 Il-F-23 Mix No. Comp. 1 comp. II M.B1.24 1 1 l-F-24 M.B1.25 1 1 l-F-25 M.B1.26 1 1 l-F-26 M.B1.27 1 1 l-F-27 M.B1.28 1 1 l-F- 28 M.B1.29 1 1 l-F-29 M.B1.30 1 1 l-F-30 M.B1.31 1 1 l-F-31 M.B1.32 1 I l-F-32 M.B1.33 1 I l-F- 33 M.B1.34 1 Il-F-34 M.B1.35 1 11-1-1 M.B1.36 1 II-I-2 M.B1.37 1 II-I-3 M.B1.38 1 II-I-4 M.B1.39 1 II-I-5 M.B1.40 1 II-I-6 M.B1.41 1 II-I-7 M.B1.42 1 II-I-8 M .B1.43 1 II-I-9 M.B1.44 1 Il-l-1 0 M.B1.45 1 11-1-11 M.B1.46 1 Il-l-1 2 Mix No. Comp. 1 comp. II M.B1.47 1 Il-l-13 M.B1.48 1 Il-l-14 M.B1.49 1 11-1-15 M.B1.50 1 11-1-16 M.B1.51 1 Il-l-1 7 Mix No. Comp. 1 comp. II M.B1.52 1 Il-l-1 8 M.B1.53 1 Il-l-1 9 M.B1.54 1 II-I-20 M.B1.55 1 11-1-21 M.B1 .56 1 II-I-22 CQQCnn / l 7Π7 / Β / ΥΙΛΙ In another embodiment of the present invention, the mixtures comprise the compound of Formula (I) and two agriculturally acceptable active components (Active Compound II and Active Compound III) selected from the compounds listed in Table B. Therefore, in this further embodiment, the mixtures comprise a compound of Formula (I) and two fungicides or two insecticides or a compound of Formula (I) and a fungicide and an insecticide, selected from Table B. Therefore, in the context of the present invention, each of the rows of Table T-1 corresponds to a mixture of Compound I (of Formula I) to be applied in the methods according to the present invention. Table T-1 Mix No. Comp. 1 comp. II Comp. III Mixture No. Comp. 1 comp. II Comp. III M.T1.1 1 1 l-F-1 I l-F-5 M.T1 .23 1 I l-F-1 I l-F-27 M.T1.2 1 I l-F-1 I l-F-6 M.T1 .24 1 I I-F-1 I I-F-28 5 M.T1.3 1 I I-F-1 I I-F-7 M.T1.25 1 I I-F-1 I I-F-29 M.T1.4 1 I I-F-1 I I-F-8 M.T1 .26 1 I I-F-1 I I-F-30 M.T1.5 1 I I-F-1 I I-F-9 M.T1.27 1 I I-F-1 I I-F-31 M.T1.6 1 I I-F -1 Il-F-1 0 M.T1 .28 1 Il-F-1 Il-F-32 M.T1.7 1 Il-F-1 Il-F-11 M.T1.29 1 Il-F-1 Il-F-33 10 M.T1.8 1 Il-F-1 Il-F-1 2 M.T1.30 1 Il-F-1 Il-F-34 M.T1.9 1 Il-F-1 Il-F-1 3 M.T1.31 1 I l-F-2 I l-F-5 M.T1.10 1 I l-F-1 I l-F-1 4 M.T1.32 1 I l-F-2 I l-F-6 M.T1.11 1 I l-F-1 I l-F- 1 5 M.T1.33 1 Il-F-2 Il-F-7 15 M.T1.12 1 Il-F-1 Il-F-1 6 M.T1.34 1 Il-F-2 Il-F-8 M.T1. 13 1 Il-F-1 Il-F-1 7 M.T1.35 1 Il-F-2 Il-F-9 M.T1.14 1 Il-F-1 Il-F-1 8 M.T1.36 1 Il-F-2 I l-F-1 0 M.T1.15 1 I l-F-1 I l-F-1 9 M.T1.37 1 I l-F-2 I l-F-11 M.T1.16 1 I l-F-1 I l-F-20 M. T1.38 1 I I-F-2 I I-F-1 2 20 M.T1.17 1 I I-F-1 I I-F-21 M.T1.39 1 I I-F-2 I I-F-13 M.T1.18 1 I I-F -1 Il-F-22 M.T1.40 1 Il-F-2 Il-F-1 4 M.T1.19 1 Il-F-1 Il-F-23 M.T1.41 1 Il-F-2 Il-F-1 5 M.T1.20 1 I l-F-1 I l-F-24 M.T1.42 1 I l-F-2 I l-F-1 6 M.T1.21 1 I l-F-1 I l-F-25 M.T1 .43 1 I I-F-2 I I-F-1 7 M.T1.22 1 I I-F-1 I I-F-26 M.T1.44 1 I I-F-2 I I-F-1 8 Mix No. Comp. 1 comp. II Comp. III Mixture No. Comp. 1 comp. II Comp. III M.T1.45 1 1 l-F-2 1 l-F-1 9 M.T1.67 1 1 l-F-3 I l-F-11 M.T1.46 1 1 l-F-2 I l-F-20 M.T1.68 1 1 l-F-3 I l-F-1 2 5 M.T1.47 1 1 l-F-2 I l-F-21 M.T1.69 1 1 l-F-3 I l-F-13 M.T1.48 1 1 l-F-2 I l-F -22 M.T1.70 1 1 l-F-3 I l-F-1 4 M.T1.49 1 1 l-F-2 I l-F-23 M.T1.71 1 1 l-F-3 I l-F-1 5 M.T1. 50 1 1 l-F-2 I l-F-24 M.T1.72 1 1 l-F-3 I l-F-1 6 M.T1.51 1 1 l-F-2 I l-F-25 M.T1.73 1 1 l-F-3 I l-F-1 7 10 M.T1.52 1 1 l-F-2 I l-F-26 M.T1.74 1 1 l-F-3 I l-F-1 8 M.T1.53 1 1 l-F-2 I l-F-27 M. T1.75 1 1 l-F-3 I l-F-1 9 M.T1.54 1 1 l-F-2 I l-F-28 M.T1.76 1 1 l-F-3 I l-F-20 M.T1.55 1 1 l-F- 2 I l-F-29 M.T1.77 1 1 l-F-3 I l-F-21 15 M.T1.56 1 1 l-F-2 I l-F-30 M.T1.78 1 1 l-F-3 I l-F-22 M. T1.57 1 1 l-F-2 I l-F-31 M.T1.79 1 1 l-F-3 I l-F-23 M.T1.58 1 1 l-F-2 I l-F-32 M.T1.80 1 1 l-F-3 I l-F-24 M.T1.59 1 1 l-F-2 I l-F-33 M.T1.81 1 1 l-F-3 I l-F-25 M.T1.60 1 1 l-F-2 I l-F-34 M.T1. 82 1 1 l-F-3 I l-F-26 20 M.T1.61 1 1 l-F-3 I l-F-5 M.T1.83 1 1 l-F-3 I l-F-27 M.T1.62 1 1 l-F-3 I l-F-6 M.T1.84 1 1 l-F-3 I l-F-28 M.T1.63 1 1 l-F-3 I l-F-7 M.T1.85 1 1 l-F-3 I l-F-29 M.T1.64 1 1 l-F-3 I l-F-8 M.T1.86 1 1 l-F-3 I l-F-30 M.T1.65 1 1 l-F-3 I l-F-9 M.T1.87 1 1 l-F-3 I l-F- 31 M.T1.66 1 1 l-F-3 I l-F-1 0 M.T1.88 1 1 l-F-3 I l-F-32 Mix comp. Comp. Comp. No. 1 II III M.T1.89 1 1 l-F-3 1 l-F-33 M.T1.90 1 1 l-F-3 1 l-F-34 M.T1.91 1 1 l-F-4 ll-F-5 M .T1.92 1 1 l-F-4 1 l-F-6 M.T1.93 1 1 l-F-4 ll-F-7 M.T1.94 1 1 l-F-4 1 l-F-8 M.T1.95 1 1 l-F -4 ll-F-9 M.T1.96 1 1 l-F-4 I l-F-1 0 M.T1.97 1 1 l-F-4 ll-F-1 1 M.T1.98 1 1 l-F-4 ll- F-1 2 M.T1.99 1 1 l-F-4 ll-F-13 M.T1.100 1 1 l-F-4 I l-F-1 4 M.T1.101 1 1 l-F-4 ll-F-1 5 M.T1.102 1 1 l-F-4 ll-F-1 6 M.T1.103 1 1 l-F-4 ll-F-1 7 M.T1.104 1 1 l-F-4 ll-F-1 8 M. T1.105 1 1 l-F-4 ll-F-1 9 M.T1.106 1 1 l-F-4 I l-F-20 M.T1.107 1 1 l-F-4 I l-F-21 M.T1.108 1 1 l-F -4 I l-F-22 M.T1.109 1 1 l-F-4 I l-F-23 M.T1.110 1 1 l-F-4 I l-F-24 Mix comp. Comp. Comp. No. 1 II III M.T1 .1 1 1 1 1 l-F-4 1 l-F-25 M.T1 .1 12 1 1 l-F-4 1 l-F-26 M.T1.113 1 1 l-F-4 1 l-F- 27 M.T1 .1 14 1 1 l-F-4 1 l-F-28 M.T1.115 1 1 l-F-4 1 l-F-29 M.T1 .1 16 1 1 l-F-4 ll-F-30 M.T1. 117 1 1 l-F-4 ll-F-31 M.T1.118 1 1 l-F-4 ll-F-32 M.T1.119 1 1 l-F-4 I l-F-33 M.T1.120 1 1 l-F-4 I l-F-34 M.T1.121 1 ll-F-5 ll-F-11 M.T1.122 1 1 l-F-5 I l-F-1 2 M.T1.123 1 ll-F-5 I l-F-1 3 M.T1.124 1 ll-F-5 I l-F-1 4 M.T1.125 1 ll-F-5 I l-F-1 5 M.T1.126 1 ll-F-5 I l-F-1 6 M .T1.127 1 ll-F-5 I l-F-1 7 M.T1.128 1 ll-F-5 I l-F-1 8 M.T1.129 1 ll-F-5 I l-F-1 9 M.T1 .130 1 ll-F-5 I 1-F-20 M.T1.131 1 ll-F-5 I 1-F-21 M.T1.132 1 ll-F-5 I 1-F-22 Mix comp. Comp. Comp. No. 1 II III M.T1.133 1 1 l-F-5 ll-F-23 M.T1.134 1 1 l-F-5 1 l-F-24 M.T1.135 1 1 l-F-5 1 l-F-25 M .T1.136 1 1 l-F-5 1 l-F-26 M.T1.137 1 1 l-F-5 1 l-F-27 M.T1.138 1 1 l-F-5 1 l-F-28 M.T1.139 1 1 l-F- 5 1 l-F-29 M.T1.140 1 1 l-F-5 ll-F-30 M.T1.141 1 1 l-F-5 1 l-F-31 M.T1.142 1 1 l-F-5 ll-F-32 M .T1.143 1 1 l-F-5 I l-F-33 M.T1.144 1 1 l-F-5 I l-F-34 M.T1.145 1 ll-F-6 ll-F-1 1 M.T1.146 1 ll-F-6 ll-F-1 2 M.T1.147 1 ll-F-6 I l-F-1 3 M.T1.148 1 ll-F-6 I l-F-1 4 M.T1.149 1 ll -F-6 ll-F-1 5 M.T1.150 1 ll-F-6 ll-F-1 6 M.T1.151 1 ll-F-6 ll-F-1 7 M.T1.152 1 ll-F-6 ll-F-1 8 M.T1.153 1 ll-F-6 ll-F-1 9 M.T1.154 1 ll-F-6 ll-F-20 Mix comp. Comp. Comp. No. 1 II III M.T1.155 1 ​​1 l-F-6 1 l-F-21 M.T1.156 1 ll-F-6 I l-F-22 M.T1.157 1 1 l-F-6 ll-F-23 M.T1.158 1 ll-F-6 I 1-F-24 M.T1.159 1 ll-F-6 I 1-F-25 M.T1.160 1 ll-F-6 I 1-F-26 M.T1.161 1 ll-F-6 I l-F-27 M.T1.162 1 ll-F-6 I l-F-28 M.T1.163 1 ll-F-6 I l-F-29 M.T1.164 1 ll-F- 6 ll-F-30 M.T1.165 1 ll-F-6 I l-F-31 M.T1.166 1 ll-F-6 ll-F-32 M.T1.167 1 ll-F-6 I l-F -33 M.T1.168 1 ll-F-6 I l-F-34 M.T1.169 1 ll-F-6 ll-F-11 M.T1.170 1 ll-F-6 I l-F-1 2 M .T1.171 1 ll-F-6 I l-F-1 3 M.T1.172 1 ll-F-6 I l-F-1 4 M.T1.173 1 ll-F-6 I l-F-1 5 M.T1 .174 1 ll-F-6 I l-F-1 6 M.T1.175 1 ll-F-6 I l-F-1 7 M.T1.176 1 ll-F-6 I l-F-1 8 Mix No. Comp. 1 comp. II Comp. III Mixture No. Comp. 1 comp. II Comp. III M.T1.177 1 1 l-F-6 1 l-F-1 9 M.T1.199 1 1 l-F-7 I l-F-1 7 M.T1.178 1 1 l-F-6 I l-F-20 M.T1 .200 1 1 l-F-7 I l-F-1 8 5 M.T1.179 1 1 l-F-6 I l-F-21 M.T1.201 1 1 l-F-7 I l-F-1 9 M.T1.180 1 1 l-F-6 I l-F-22 M.T1 .202 1 1 l-F-7 I l-F-20 M.T1.181 1 1 l-F-6 I l-F-23 M.T1.203 1 1 l-F-7 I l-F-21 M.T1. 182 1 1 l-F-6 I l-F-24 M.T1 .204 1 1 l-F-7 I l-F-22 M.T1.183 1 1 l-F-6 I l-F-25 M.T1.205 1 1 l-F-7 I l-F -23 10 M.T1.184 1 1 l-F-6 I l-F-26 M.T1.206 1 1 l-F-7 I l-F-24 M.T1.185 1 1 l-F-6 I l-F-27 M.T1.207 1 1 l-F-7 I l-F-25 M.T1.186 1 1 l-F-6 I l-F-28 M.T1.208 1 1 l-F-7 I l-F-26 M.T1.187 1 1 l-F-6 I l-F- 29 M.T1.209 1 1 l-F-7 I l-F-27 15 M.T1.188 1 1 l-F-6 I l-F-30 M.T1.210 1 1 l-F-7 I l-F-28 M.T1.189 1 1 l-F-6 I l-F-31 M.T1.21 1 1 1 l-F-7 I l-F-29 M.T1.190 1 1 l-F-6 I l-F-32 M.T1 .212 1 1 l-F-7 I l-F- 30 M.T1.191 1 1 l-F-6 I l-F-33 M.T1.213 1 1 l-F-7 I l-F-31 M.T1.192 1 1 l-F-6 I l-F-34 M.T1.214 1 1 l-F-7 I l-F-32 20 M.T1.193 1 1 l-F-7 I l-F-11 M.T1.215 1 1 l-F-7 I l-F-33 M.T1.194 1 1 l-F-7 I l-F-1 2 M.T1.216 1 1 l-F-7 I l-F-34 M.T1.195 1 1 l-F-7 I l-F-1 3 M.T1.217 1 1 l-F-8 I l-F-11 M.T1.196 1 1 l-F-7 I l-F-1 4 M.T1.218 1 1 l-F-8 I l-F-1 2 M.T1.197 1 1 l-F-7 I l-F-1 5 M.T1 .219 1 1 l-F-8 I l-F-13 M.T1.198 1 1 l-F-7 I l-F-1 6 M.T1.220 1 1 l-F-8 I l-F-1 4 Mix No. Comp. 1 comp. II Comp. III Mixture No. Comp. 1 comp. II Comp. III M.T1.221 1 1 l-F-8 1 l-F-1 5 M.T1 .243 1 1 l-F-9 I l-F-13 M.T1.222 1 1 l-F-8 I l-F-1 6 M.T1 .244 1 1 l-F-9 I l-F-1 4 5 M.T1.223 1 1 l-F-8 I l-F-1 7 M.T1.245 1 1 l-F-9 I l-F-1 5 M.T1.224 1 1 l-F- 8 I l-F-1 8 M.T1 .246 1 1 l-F-9 I l-F-1 6 M.T1.225 1 1 l-F-8 I l-F-1 9 M.T1.247 1 1 l-F-9 I l-F-1 7 M.T1.226 1 1 l-F-8 I l-F-20 M.T1 .248 1 1 l-F-9 I l-F-1 8 M.T1.227 1 1 l-F-8 I l-F-21 M.T1.249 1 1 l-F-9 I l-F-1 9 10 M.T1.228 1 1 l-F-8 I l-F-22 M.T1.250 1 1 l-F-9 I l-F-20 M.T1.229 1 1 l-F-8 I l-F -23 M.T1.251 1 1 l-F-9 I l-F-21 M.T1.230 1 1 l-F-8 I l-F-24 M.T1.252 1 1 l-F-9 I l-F-22 M.T1.231 1 1 l-F-8 I l-F-25 M.T1.253 1 1 l-F-9 I l-F-23 15 M.T1.232 1 1 l-F-8 I l-F-26 M.T1.254 1 1 l-F-9 I l-F- 24 M.T1.233 1 1 l-F-8 I l-F-27 M.T1.255 1 1 l-F-9 I l-F-25 M.T1.234 1 1 l-F-8 I l-F-28 M.T1.256 1 1 l-F-9 I l-F-26 M.T1.235 1 1 l-F-8 I l-F-29 M.T1.257 1 1 l-F-9 I l-F-27 M.T1.236 1 1 l-F-8 I l-F-30 M .T1.258 1 1 l-F-9 I l-F-28 20 M.T1.237 1 1 l-F-8 I l-F-31 M.T1.259 1 1 l-F-9 I l-F-29 M.T1.238 1 1 l-F -8 I l-F-32 M.T1.260 1 1 l-F-9 I l-F-30 M.T1.239 1 1 l-F-8 I l-F-33 M.T1.261 1 1 l-F-9 I l-F-31 M. T1.240 1 1 l-F-8 I l-F-34 M.T1.262 1 1 l-F-9 I l-F-32 M.T1.241 1 1 l-F-9 I l-F-11 M.T1 .263 1 1 l-F-9 I I-F-33 M.T1.242 1 1 I-F-9 I I-F-1 2 M.T1.264 1 1 I-F-9 I I-F-34 100 Mix comp. Comp. Comp. No. 1 II III M.T1.265 1 1 I-F-1 0 I I-F-11 M.T1.266 1 I I-F-1 0 I I-F-1 2 M.T1.267 1 ll-F-10 I I-F -1 3 M.T1.268 1 Il-F-1 0 Il-F-1 4 M.T1.269 1 ll-F-10 Il-F-1 5 M.T1.270 1 ll-F-10 Il-F-1 6 M.T1.271 1 ll-F-10 I l-F-1 7 M.T1.272 1 ll-F-10 I l-F-1 8 M.T1.273 1 ll-F-10 I l-F-1 9 M .T1.274 1 ll-F-10 ll-F-20 M.T1.275 1 ll-F-10 I l-F-21 M.T1.276 1 ll-F-10 I l-F-22 M.T1.277 1 ll-F-10 I l-F-23 M.T1.278 1 ll-F-10 I l-F-24 M.T1.279 1 ll-F-10 I l-F-25 M.T1.280 1 ll-F- 10 I l-F-26 M.T1.281 1 ll-F-10 I l-F-27 M.T1.282 1 ll-F-10 I l-F-28 M.T1.283 1 ll-F-10 ll-F- 29 M.T1.284 1 ll-F-10 I l-F-30 M.T1.285 1 ll-F-10 I l-F-31 M.T1.286 1 ll-F-10 I l-F-32 Mix comp. Comp. Comp. No. 1 II III M.T1 .287 1 ll-F-10 I l-F-33 M.T1 .288 1 ll-F-10 I l-F-34 M.T1.289 1 I l-F-11 I l-F-1 7 M.T1 .290 1 Il-F-11 Il-F-1 8 M.T1.291 1 Il-F-11 Il-F-1 9 M.T1 .292 1 Il-F-11 ll-F-20 M.T1. 293 1 I I-F-11 I I-F-21 M.T1.294 1 I I-F-11 I I-F-22 M.T1.295 1 I I-F-11 I I-F-23 M.T1.296 1 I I-F-11 I I-F -24 M.T1.297 1 I I-F-11 ll-F-25 M.T1.298 1 I I-F-11 I I-F-26 M.T1.299 1 I I-F-11 I I-F-27 M.T1.300 1 I I-F-11 I I-F-28 M.T1.301 1 I I-F-11 ll-F-29 M.T1.302 1 I I-F-11 I I-F-30 M.T1.303 1 I I-F-11 I I-F -31 M.T1.304 1 I I-F-11 I I-F-32 M.T1.305 1 I I-F-11 I I-F-33 M.T1.306 1 I I-F-11 I I-F-34 M.T1 .307 1 ll-F-1 2 Il-F-1 7 M.T1.308 1 ll-F-1 2 Il-F-1 8 CQQCnn / l 7Π7 / Β / Υ 101 Mix No. Comp. 1 comp. II Comp. III Mixture No. Comp. 1 comp. II Comp. III M.T1.309 1 1 l-F-1 2 I l-F-1 9 M.T1.331 1 I l-F-1 3 I l-F-23 M.T1.310 1 I l-F-1 2 I l-F-20 M.T1 .332 1 ll-F-1 3 Il-F-24 5 M.T1.311 1 Il-F-1 2 Il-F-21 M.T1.333 1 Il-F-1 3 Il-F-25 M.T1.312 1 I l-F-1 2 I l-F-22 M.T1 .334 1 ll-F-1 3 I l-F-26 M.T1.313 1 I l-F-1 2 I l-F-23 M.T1.335 1 ll-F- 1 3 Il-F-27 M.T1.314 1 Il-F-1 2 Il-F-24 M.T1.336 1 ll-F-1 3 Il-F-28 M.T1.315 1 Il-F-1 2 Il-F -25 M.T1.337 1 ll-F-1 3 I l-F-29 10 M.T1.316 1 I l-F-1 2 I l-F-26 M.T1.338 1 ll-F-1 3 I l-F-30 M.T1.317 1 Il-F-1 2 Il-F-27 M.T1.339 1 ll-F-1 3 Il-F-31 M.T1.318 1 Il-F-1 2 Il-F-28 M.T1. 340 1 ll-F-1 3 Il-F-32 M.T1.319 1 Il-F-1 2 Il-F-29 M.T1.341 1 ll-F-1 3 Il-F-33 15 M.T1.320 1 I l-F-1 2 I l-F-30 M.T1.342 1 ll-F-1 3 I l-F-34 M.T1.321 1 I l-F-1 2 I l-F-31 M.T1.343 1 ll-F- 1 4 Il-F-1 7 M.T1.322 1 Il-F-1 2 Il-F-32 M.T1.344 1 ll-F-1 4 Il-F-1 8 M.T1.323 1 Il-F-1 2 I l-F-33 M.T1.345 1 ll-F-1 4 I l-F-1 9 M.T1.324 1 I l-F-1 2 I l-F-34 M.T1.346 1 ll-F-1 4 I l-F -20 20 M.T1.325 1 I l-F-1 3 I l-F-1 7 M.T1.347 1 ll-F-1 4 I l-F-21 M.T1.326 1 I l-F-1 3 I l-F-1 8 M.T1.348 1 ll-F-1 4 I l-F-22 M.T1.327 1 I l-F-1 3 I l-F-1 9 M.T1.349 1 ll-F-1 4 I l-F-23 M .T1.328 1 Il-F-1 3 Il-F-20 M.T1.350 1 ll-F-1 4 Il-F-24 M.T1.329 1 Il-F-1 3 Il-F-21 M.T1 .351 1 ll-F-1 4 Il-F-25 M.T1.330 1 Il-F-1 3 Il-F-22 M.T1.352 1 ll-F-1 4 Il-F-26 CQQCnn / l 7Π7 / Β / ΥΙΛΙ 102 Mix comp. Comp. Comp. No. 1 II III M.T1.353 1 ll-F-14 I l-F-27 M.T1.354 1 ll-F-14 I l-F-28 M.T1.355 1 ll-F-14 ll-F -29 M.T1.356 1 ll-F-14 I l-F-30 M.T1.357 1 ll-F-14 I l-F-31 M.T1.358 1 ll-F-14 I l-F-32 M.T1 .359 1 ll-F-14 I l-F-33 M.T1.360 1 ll-F-14 I l-F-34 M.T1.361 1 I l-F-1 5 I l-F-1 7 M.T1.362 1 I I-F-1 5 I I-F-1 8 M.T1.363 1 I I-F-1 5 I I-F-1 9 M.T1.364 1 I I-F-1 5 ll-F-20 M.T1.365 1 I I-F- 1 5 I l-F-21 M.T1.366 1 I l-F-1 5 I l-F-22 M.T1.367 1 I l-F-1 5 I l-F-23 M.T1.368 1 I l-F-1 5 I l-F- 24 M.T1.369 1 Il-F-1 5 ll-F-25 M.T1.370 1 Il-F-1 5 Il-F-26 M.T1.371 1 Il-F-1 5 Il-F-27 M.T1 .372 1 Il-F-1 5 Il-F-28 M.T1.373 1 Il-F-1 5 ll-F-29 M.T1.374 1 Il-F-1 5 Il-F-30 Mix comp. Comp. Comp. No. 1 II III M.T1 .375 1 ll-F-1 5 ll-F-31 M.T1.376 1 ll-F-1 5 I l-F-32 M.T1.377 1 ll-F-1 5 I l-F-33 M.T1 .378 1 ll-F-1 5 I l-F-34 M.T1.379 1 ll-F-1 6 I l-F-1 7 M.T1.380 1 ll-F-1 6 I l-F-1 8 M.T1.381 1 ll-F-1 6 I l-F-1 9 M.T1.382 1 ll-F-1 6 ll-F-20 M.T1.383 1 ll-F-1 6 I l-F-21 M.T1.384 1 ll-F-1 6 I l-F-22 M.T1.385 1 ll-F-1 6 I l-F-23 M.T1.386 1 ll-F-1 6 I l-F-24 M.T1.387 1 ll-F-1 6 ll-F-25 M.T1.388 1 ll-F-1 6 I l-F-26 M.T1.389 1 ll-F-1 6 I l-F -27 M.T1.390 1 ll-F-1 6 I l-F-28 M.T1.391 1 ll-F-1 6 ll-F-29 M.T1.392 1 ll-F-1 6 I l-F- 30 M.T1.393 1 ll-F-1 6 ll-F-31 M.T1.394 1 ll-F-1 6 I l-F-32 M.T1.395 1 ll-F-1 6 I l-F-33 M.T1.396 1 ll-F-1 6 I 1-F-34 CQQcnn / ι ζηζ / Ε / γ 103 Mix comp. Comp. Comp. No. 1 II III M.T1.397 1 1 l-F-1 7 I l-F-28 M.T1.398 1 I l-F-1 7 I l-F-29 M.T1.399 1 I l-F-1 7 I l-F- 30 M.T1.400 1 Il-F-1 7 Il-F-31 M.T1.401 1 Il-F-1 7 Il-F-32 M.T1.402 1 Il-F-1 7 Il-F-33 M.T1. 403 1 Il-F-1 7 Il-F-34 M.T1.404 1 Il-F-1 8 Il-F-28 M.T1.405 1 Il-F-1 8 Il-F-29 M.T1.406 1 Il-F- 1 8 Il-F-30 M.T1.407 1 Il-F-1 8 ll-F-31 M.T1.408 1 Il-F-1 8 Il-F-32 M.T1.409 1 Il-F-1 8 Il-F -33 M.T1.410 1 I l-F-1 8 I l-F-34 M.T1.411 1 I l-F-1 9 I l-F-28 M.T1.412 1 I l-F-1 9 I l-F-29 M.T1 .413 1 I l-F-1 9 I l-F-30 M.T1.414 1 I l-F-1 9 ll-F-31 M.T1.415 1 I l-F-1 9 I l-F-32 M.T1.416 1 I I-F-1 9 I I-F-33 M.T1.417 1 I I-F-1 9 I I-F-34 M.T1.418 1 I I-F-20 I I-F-28 Mix comp. Comp. Comp. No. 1 II III M.T1 .419 1 1 l-F-20 I l-F-29 M.T1 .420 1 1 l-F-20 I l-F-30 M.T1.421 1 1 l-F-20 ll-F-31 M .T1 .422 1 1 l-F-20 I l-F-32 M.T1.423 1 1 l-F-20 I l-F-33 M.T1 .424 1 1 l-F-20 I l-F-34 M.T1.425 1 1 l-F- 21 I I-F-28 M.T1.426 1 I I-F-21 I I-F-29 M.T1.427 1 ll-F-21 I I-F-30 M.T1.428 1 I I-F-21 ll-F-31 M .T1.429 1 ll-F-21 I l-F-32 M.T1.430 1 ll-F-21 I l-F-33 M.T1.431 1 ll-F-21 I l-F-34 M.T1.432 1 I I-F-22 I I-F-28 M.T1.433 1 I I-F-22 I I-F-29 M.T1.434 1 I I-F-22 I I-F-30 M.T1.435 1 I I-F-22 ll-F- 31 M.T1.436 1 I l-F-22 I l-F-32 M.T1.437 1 I l-F-22 I l-F-33 M.T1.438 1 I l-F-22 I l-F-34 M.T1 .439 1 I I-F-23 I I-F-28 M.T1.440 1 I I-F-23 I I-F-29 CQQCnn / l 7Π7 / Β / Υ 104 Mix comp. Comp. Comp. No. 1 II III M.T1.441 1 1 l-F-23 1 l-F-30 M.T1.442 1 1 l-F-23 1 l-F-31 M.T1.443 1 1 l-F-23 I l-F-32 M. T1.444 1 1 l-F-23 I l-F-33 M.T1.445 1 1 l-F-23 I l-F-34 M.T1.446 1 1 l-F-24 I l-F-28 M.T1.447 1 1 l-F-24 I l-F-29 M.T1.448 1 1 l-F-24 I l-F-30 M.T1.449 1 1 l-F-24 I l-F-31 M.T1.450 1 1 l-F-24 I l-F-32 M.T1. 451 1 1 l-F-24 I l-F-33 M.T1.452 1 1 l-F-24 I l-F-34 M.T1.453 1 1 l-F-25 I l-F-28 M.T1.454 1 1 l-F-25 I l-F -29 M.T1.455 1 1 l-F-25 I l-F-30 M.T1.456 1 1 l-F-25 I l-F-31 M.T1.457 1 1 l-F-25 I l-F-32 M.T1.458 1 1 l-F-25 I l-F-33 M.T1.459 1 1 l-F-25 I l-F-34 M.T1.460 1 1 l-F-26 I l-F-28 M.T1.461 1 1 l-F-26 I l-F-29 M.T1.462 1 1 l-F-26 I l-F-30 Mix comp. Comp. Comp. No. 1 II III M.T1 .463 1 1 l-F-26 1 l-F-31 M.T1 .464 1 1 l-F-26 I l-F-32 M.T1.465 1 1 l-F-26 I l-F-33 M. T1 .466 1 1 l-F-26 I l-F-34 M.T1.467 1 1 l-F-27 I l-F-28 M.T1.468 1 1 l-F-27 I l-F-29 M.T1.469 1 1 l-F-27 ll-F-30 M.T1.470 1 1 l-F-27 I l-F-31 M.T1.471 1 1 l-F-27 I l-F-32 M.T1.472 1 1 l-F-27 I l-F-33 M.T1 .473 1 1 l-F-27 I l-F-34 M.T1.474 1 1 l-F-28 I l-F-29 M.T1.475 1 1 l-F-28 ll-F-30 M.T1.476 1 1 l-F-28 I l-F-31 M.T1.477 1 1 l-F-28 I l-F-32 M.T1.478 1 1 l-F-28 I l-F-33 M.T1.479 1 1 l-F-28 I l-F-34 M.T1. 480 1 1 l-F-30 I l-F-29 M.T1.481 1 ll-F-30 I l-F-31 M.T1.482 1 ll-F-30 I l-F-32 M.T1 .483 1 ll-F- 30 Il-F-33 M.T1.484 1 ll-F-30 Il-F-34 CQQCnn / l 7Π7 / Β / Υ 105 Mix No. Comp. 1 comp. II Comp. III M.T1.485 1 1 l-F-29 I l-F-31 M.T1.486 1 1 l-F-29 I l-F-32 M.T1.487 1 1 l-F-29 I l-F-33 M.T1.488 1 1 I-F-29 I I-F-34 M.T1.489 1 11-1-1 I I-F-1 M.T1.490 1 11-1-1 I I-F-2 M.T1.491 1 11-1-1 I I-F -3 M.T1.492 1 11-1-1 I l-F-4 M.T1.493 1 11-1-1 ll-F-5 M.T1.494 1 11-1-1 I l-F-6 M. T1.495 1 11-1-1 ll-F-7 M.T1.496 1 11-1-1 I l-F-8 M.T1.497 1 11-1-1 ll-F-9 M.T1.498 1 11-1-1 I l-F-1 0 M.T1.499 1 11-1-1 I l-F-11 M.T1.500 1 11-1-1 I l-F-1 2 M.T1.501 1 11- 1-1 I l-F-1 3 M.T1.502 1 11-1-1 I l-F-1 4 M.T1.503 1 11-1-1 I l-F-1 5 M.T1.504 1 11-1- 1 Il-F-1 6 M.T1.505 1 11-1-1 Il-F-1 7 Mix No. Comp. 1 comp. II Comp. III M.T1.506 1 II- 1-1 I l-F-1 8 M.T1 .507 1 II- 1-1 I l-F-1 9 M.T1.508 1 II- 1-1 I l-F-20 M. T1.509 1 II- 1-1 I I-F-21 M.T1.510 1 II- 1-1 I I-F-22 M.T1.51 1 1 II- 1-1 I I-F-23 M.T1.512 1 II- 1-1 I I-F-24 M.T1.513 1 II- 1-1 I I-F-25 M.T1.514 1 II- 1-1 I I-F-26 M.T1.515 1 II- 1-1 I I-F-27 M.T1.516 1 II- 1-1 I I-F-28 M.T1.517 1 II- 1-1 I I-F-29 M.T1.518 1 II- 1-1 ll-F-30 M.T1.519 1 II- 1-1 ll-F-31 M.T1.520 1 II- 1-1 I l-F-32 M.T1.521 1 II- 1-1 I l-F-33 M.T1. 522 1 II- 1-1 I l-F-34 M.T1.523 1 II- 1-1 II-I-22 M.T1.524 1 II- I-2 I l-F-1 M.T1.525 1 II- I-2 I I-F-2 M.T1 .526 1 II- I-2 I I-F-3 M.T1.527 1 II- I-2 I I-F-4 CQQCnn / l 7Π7 / Β / Υ 106 Mix No. Comp. 1 comp. II Comp. III Mixture No. Comp. 1 comp. II Comp. III M.T1.528 1 11-1-2 1 l-F-5 M.T1.550 1 11-1-2 1 l-F-27 M.T1.529 1 11-1-2 1 l-F-6 M.T1. 551 1 11-1-2 1 l-F-28 5 M.T1.530 1 11-1-2 1 l-F-7 M.T1.552 1 11-1-2 1 l-F-29 M.T1.531 1 11- 1-2 1 l-F-8 M.T1.553 1 II-1-2 1 l-F-30 M.T1.532 1 11-1-2 1 l-F-9 M.T1.554 1 11-1-2 1 l-F -31 M.T1.533 1 11-1-2 1 l-F-1 0 M.T1.555 1 11-1-2 I l-F-32 M.T1.534 1 11-1-2 I l-F-11 M. T1.556 1 11-1-2 I l-F-33 10 M.T1.535 1 11-1-2 I l-F-1 2 M.T1.557 1 II-1-2 I l-F-34 M.T1.536 1 11-1-2 I l-F-1 3 M.T1.558 1 II-1-2 II-I-22 M.T1.537 1 11-1-2 I l-F-1 4 M.T1.559 1 11 -1-3 Il-F-1 M.T1.538 1 11-1-2 Il-F-1 5 M.T1.560 1 11-1-3 Il-F-2 15 M.T1.539 1 11-1- 2 I I-F-1 6 M.T1.561 1 11-1-3 I I-F-3 M.T1.540 1 11-1-2 I I-F-1 7 M.T1.562 1 II-1-3 I I-F -4 M.T1.541 1 11-1-2 I l-F-1 8 M.T1.563 1 11-1-3 I l-F-5 M.T1.542 1 11-1-2 I l-F-1 9 M .T1.564 1 11-1-3 I l-F-6 M.T1.543 1 11-1-2 I l-F-20 M.T1.565 1 11-1-3 I l-F-7 20 M.T1.544 1 11-1-2 I I-F-21 M.T1.566 1 II-1-3 I I-F-8 M.T1.545 1 11-1-2 I I-F-22 M.T1.567 1 II-1- 3 I l-F-9 M.T1.546 1 11-1-2 I l-F-23 M.T1.568 1 11-1-3 I l-F-1 0 M.T1.547 1 11-1-2 I l-F- 24 M.T1.569 1 11-1-3 I l-F-11 M.T1.548 1 11-1-2 I l-F-25 M.T1.570 1 11-1-3 I l-F-1 2 M.T1 .549 1 11-1-2 I I-F-26 M.T1.571 1 II-1-3 I I-F-13 CQQCnn / l 7Π7 / Β / Υ 107 Mix No. Comp. 1 comp. II Comp. III Mixture No. Comp. 1 comp. II Comp. III M.T1.572 1 11-1-3 1 l-F-1 4 M.T1 .594 1 11-1-4 I l-F-1 M.T1.573 1 11-1-3 I l-F-1 5 M. T1.595 1 11-1-4 I l-F-2 5 M.T1.574 1 11-1-3 I l-F-1 6 M.T1.596 1 11-1-4 I l-F-3 M.T1.575 1 11-1-3 I l-F-1 7 M.T1 .597 1 II-1-4 I l-F-4 M.T1.576 1 11-1-3 I l-F-1 8 M.T1.598 1 11- 1-4 I l-F-5 M.T1.577 1 11-1-3 I l-F-1 9 M.T1.599 1 11-1-4 I l-F-6 M.T1.578 1 11-1-3 I I-F-20 M.T1.600 1 11-1-4 I I-F-7 10 M.T1.579 1 11-1-3 I I-F-21 M.T1.601 1 II-1-4 I I-F-8 M .T1.580 1 11-1-3 I I-F-22 M.T1.602 1 II-1-4 I I-F-9 M.T1.581 1 11-1-3 I I-F-23 M.T1.603 1 11-1-4 I I-F-1 0 M.T1.582 1 11-1-3 I I-F-24 M.T1.604 1 11-1-4 I I-F-11 15 M.T1.583 1 11-1 -3 ll-F-25 M.T1.605 1 11-1-4 I l-F-1 2 M.T1.584 1 11-1-3 ll-F-26 M.T1.606 1 II-1-4 I I-F-13 M.T1.585 1 11-1-3 I I-F-27 M.T1.607 1 11-1-4 I I-F-1 4 M.T1.586 1 11-1-3 I I-F-28 M.T1.608 1 11-1-4 I l-F-1 5 M.T1.587 1 11-1-3 I l-F-29 M.T1.609 1 11-1-4 I l-F-1 6 20 M. T1.588 1 11-1-3 I I-F-30 M.T1.610 1 II-1-4 I I-F-1 7 M.T1.589 1 11-1-3 I I-F-31 M.T1.61 1 1 II-1-4 I l-F-1 8 M.T1.590 1 11-1-3 I l-F-32 M.T1.612 1 11-1-4 I l-F-1 9 M.T1.591 1 11- 1-3 I I-F-33 M.T1.613 1 11-1-4 I I-F-20 M.T1.592 1 11-1-3 I I-F-34 M.T1 .614 1 11-1-4 I I-F -21 M.T1.593 1 11-1-3 II-I-22 M.T1.615 1 II-1-4 I I-F-22 CQQCnn / l 7Π7 / Β / Υ 108 Mix No. Comp. 1 comp. II Comp. III Mixture No. Comp. 1 comp. II Comp. III M.T1.616 1 11-1-4 1 l-F-23 M.T1.638 1 11-1-5 I l-F-1 0 M.T1.617 1 11-1-4 1 l-F-24 M.T1 .639 1 11-1-5 ll-F-1 1 5 M.T1.618 1 11-1-4 ll-F-25 M.T1.640 1 11-1-5 I l-F-1 2 M.T1 .619 1 11-1-4 1 l-F-26 M.T1.641 1 II-1-5 I l-F-13 M.T1.620 1 11-1-4 1 l-F-27 M.T1.642 1 11- 1-5 I l-F-1 4 M.T1.621 1 11-1-4 1 l-F-28 M.T1.643 1 11-1-5 I l-F-1 5 M.T1.622 1 11-1-4 1 l-F-29 M.T1.644 1 11-1-5 I l-F-1 6 10 M.T1.623 1 11-1-4 1 l-F-30 M.T1.645 1 II-1-5 I l-F- 1 7 M.T1.624 1 11-1-4 I l-F-31 M.T1.646 1 II-1-5 I l-F-1 8 M.T1.625 1 11-1-4 I l-F-32 M. T1.647 1 11-1-5 I l-F-1 9 M.T1.626 1 11-1-4 I l-F-33 M.T1.648 1 11-1-5 I l-F-20 15 M.T1.627 1 11-1-4 I l-F-34 M.T1.649 1 11-1-5 ll-F-21 M.T1.628 1 11-1-4 II-I-22 M.T1.650 1 II- 1-5 I I-F-22 M.T1.629 1 11-1-5 ll-F-1 M.T1.651 1 11-1-5 I I-F-23 M.T1.630 1 11-1-5 I I-F-2 M.T1.652 1 11-1-5 I I-F-24 M.T1.631 1 11-1-5 I I-F-3 M.T1.653 1 11-1-5 ll-F-25 20 M.T1.632 1 11-1-5 I l-F-4 M.T1.654 1 II-1-5 I l-F-26 M.T1.633 1 11-1-5 I l-F-5 M.T1.655 1 II-1-5 I I-F-27 M.T1.634 1 11-1-5 I I-F-6 M.T1.656 1 11-1-5 I I-F-28 M.T1.635 1 11-1- 5 I I-F-7 M.T1.657 1 11-1-5 I I-F-29 M.T1.636 1 11-1-5 I I-F-8 M.T1.658 1 11-1-5 I I-F-30 M.T1.637 1 11-1-5 ll-F-9 M.T1.659 1 II-1-5 ll-F-31 CQQCnn / l 7Π7 / Β / Υ 109 Mix No. Comp. 1 comp. II Comp. III Mixture No. Comp. 1 comp. II Comp. III M.T1.660 1 11-1-5 1 l-F-32 M.T1.682 1 11-1-6 I l-F-1 9 M.T1.661 1 11-1-5 1 l-F-33 M.T1 .683 1 11-1-6 I I-F-20 5 M.T1.662 1 11-1-5 1 I-F-34 M.T1.684 1 11-1-6 I I-F-21 M.T1.663 1 11 -1-5 11-1-22 M.T1.685 1 II-1-6 I l-F-22 M.T1.664 1 11-1-6 I l-F-1 M.T1.686 1 11-1-6 I I-F-23 M.T1.665 1 11-1-6 I I-F-2 M.T1.687 1 11-1-6 I I-F-24 M.T1.666 1 11-1-6 I I-F-3 M .T1.688 1 11-1-6 I l-F-25 10 M.T1.667 1 11-1-6 I l-F-4 M.T1.689 1 II-1-6 I l-F-26 M.T1.668 1 11-1-6 ll-F-5 M.T1.690 1 II-1-6 I 1-F-27 M.T1.669 1 11-1-6 I 1-F-6 M.T1.691 1 11-1 -6 I l-F-28 M.T1.670 1 11-1-6 ll-F-7 M.T1.692 1 11-1-6 I l-F-29 15 M.T1.671 1 11-1-6 I I-F-8 M.T1.693 1 11-1-6 I I-F-30 M.T1.672 1 11-1-6 ll-F-9 M.T1.694 1 II-1-6 ll-F-31 M.T1.673 1 11-1-6 I l-F-1 0 M.T1.695 1 11-1-6 I l-F-32 M.T1.674 1 11-1-6 I l-F-11 M.T1. 696 1 11-1-6 I I-F-33 M.T1.675 1 11-1-6 I I-F-1 2 M.T1.697 1 11-1-6 I I-F-34 20 M.T1.676 1 11 -1-6 I l-F-1 3 M.T1.698 1 II-1-6 II-I-22 M.T1.677 1 11-1-6 I l-F-1 4 M.T1.699 1 II-1 -7 I l-F-1 M.T1.678 1 11-1-6 I l-F-1 5 M.T1.700 1 11-1-7 I l-F-2 M.T1.679 1 11-1-6 I l-F -1 6 M.T1.701 1 11-1-7 I l-F-3 M.T1.680 1 11-1-6 I l-F-1 7 M.T1 .702 1 11-1-7 I l-F-4 M .T1.681 1 11-1-6 I l-F-1 8 M.T1.703 1 II-1-7 ll-F-5 CQQCnn / l 7Π7 / Β / Υ 110 Mix No. Comp. 1 comp. II Comp. III Mixture No. Comp. 1 comp. II Comp. III M.T1.704 1 11-1-7 1 l-F-6 M.T1 .726 1 11-1-7 1 l-F-28 M.T1.705 1 11-1-7 1 l-F-7 M.T1 . 727 1 11-1-7 1 l-F-29 5 M.T1.706 1 11-1-7 1 l-F-8 M.T1.728 1 11-1-7 ll-F-30 M.T1.707 1 11 -1-7 1 l-F-9 M.T1 .729 1 II-1-7 ll-F-31 M.T1.708 1 11-1-7 I l-F-1 0 M.T1.730 1 11-1- 7 ll-F-32 M.T1.709 1 11-1-7 I l-F-11 M.T1.731 1 11-1-7 I l-F-33 M.T1.710 1 11-1-7 I l-F- 1 2 M.T1.732 1 11-1-7 I I-F-34 10 M.T1.711 1 11-1-7 I I-F-1 3 M.T1.733 1 II-1-7 II-I-22 M.T1.712 1 11-1-7 I l-F-1 4 M.T1.734 1 II-1-8 I l-F-1 M.T1.713 1 11-1-7 I l-F-1 5 M.T1 .735 1 11-1-8 I I-F-2 M.T1.714 1 11-1-7 ll-F-16 M.T1.736 1 11-1-8 I I-F-3 15 M.T1.715 1 11-1-7 I I-F-1 7 M.T1.737 1 11-1-8 I I-F-4 M.T1.716 1 11-1-7 I I-F-1 8 M.T1.738 1 II-1 -8 I l-F-5 M.T1.717 1 11-1-7 I l-F-1 9 M.T1.739 1 11-1-8 I l-F-6 M.T1.718 1 11-1-7 I l-F -20 M.T1.740 1 11-1-8 I l-F-7 M.T1.719 1 11-1-7 I l-F-21 M.T1.741 1 11-1-8 I l-F-8 20 M. T1.720 1 11-1-7 I l-F-22 M.T1.742 1 II-1-8 I l-F-9 M.T1.721 1 11-1-7 I l-F-23 M.T1.743 1 II -1-8 I I-F-1 0 M.T1.722 1 11-1-7 I I-F-24 M.T1.744 1 11-1-8 I I-F-11 M.T1.723 1 11-1-7 I l-F-25 M.T1.745 1 11-1-8 I l-F-1 2 M.T1.724 1 11-1-7 ll-F-26 M.T1 .746 1 11-1-8 I l-F- 13 M.T1.725 1 11-1-7 I I-F-27 M.T1.747 1 II-1-8 I I-F-1 4 CQQCnn / l 7Π7 / Β / Υ 111 Mix No. Comp. 1 comp. II Comp. III Mixture No. Comp. 1 comp. II Comp. III M.T1.748 1 11-1-8 ll-F-1 5 M.T1.770 1 11-1-9 1 1-F-2 M.T1.749 1 11-1-8 ll-F-1 6 M.T1.771 1 11-1-9 1 l-F-3 5 M.T1.750 1 11-1-8 ll-F-1 7 M.T1.772 1 11-1-9 1 l-F-4 M. T1.751 1 11-1-8 ll-F-1 8 M.T1.773 1 II-1-9 1 l-F-5 M.T1.752 1 11-1-8 ll-F-1 9 M.T1 .774 1 11-1-9 ll-F-6 M.T1.753 1 11-1-8 ll-F-20 M.T1 .775 1 11-1-9 1 1-F-7 M.T1.754 1 11-1-8 I I-F-21 M.T1.776 1 11-1-9 1 I-F-8 10 M.T1.755 1 11-1-8 I I-F-22 M.T1.777 1 II-1- 9 1 l-F-9 M.T1.756 1 11-1-8 ll-F-23 M.T1.778 1 II-1-9 I l-F-1 0 M.T1.757 1 11-1-8 I l-F -24 M.T1.779 1 11-1-9 ll-F-11 M.T1.758 1 11-1-8 I l-F-25 M.T1.780 1 11-1-9 ll-F-12 15 M.T1.759 1 11-1-8 I I-F-26 M.T1.781 1 11-1-9 I I-F-13 M.T1.760 1 11-1-8 I I-F-27 M.T1.782 1 II-1-9 I I-F-1 4 M.T1.761 1 11-1-8 I I-F-28 M.T1.783 1 11-1-9 I I-F-1 5 M.T1.762 1 11- 1-8 I I-F-29 M.T1.784 1 11-1-9 I I-F-1 6 M.T1.763 1 11-1-8 ll-F-30 M.T1.785 1 11-1-9 I l-F-1 7 20 M.T1.764 1 11-1-8 I l-F-31 M.T1.786 1 II-1-9 I l-F-1 8 M.T1.765 1 11-1-8 ll- F-32 M.T1.787 1 II-1-9 I l-F-1 9 M.T1.766 1 11-1-8 I l-F-33 M.T1.788 1 11-1-9 ll-F-20 M.T1.767 1 11-1-8 I l-F-34 M.T1.789 1 11-1-9 I l-F-21 M.T1.768 1 11-1-8 II-I-22 M.T1 . 790 1 11-1-9 I l-F-22 M.T1.769 1 11-1-9 ll-F-1 M.T1.791 1 II-1-9 ll-F-23 112 Mix No. Comp. 1 comp. II Comp. III Mixture No. Comp. 1 comp. II Comp. III M.T1.792 1 11-1-9 I l-F-24 M.T1 .814 1 11-1-1 0 I l-F-11 M.T1.793 1 11-1-9 I l-F-25 M.T1 .815 1 11-1-1 0 I l-F-1 2 5 M.T1.794 1 11-1-9 I l-F-26 M.T1.816 1 11-1-1 0 I l-F-13 M.T1. 795 1 11-1-9 I I-F-27 M.T1 .817 1 11-1-1 0 I I-F-1 4 M.T1.796 1 11-1-9 I I-F-28 M.T1.818 1 11 -1-1 0 Il-F-1 5 M.T1.797 1 11-1-9 Il-F-29 M.T1.819 1 11-1-1 0 Il-F-1 6 M.T1.798 1 11- 1-9 I I-F-30 M.T1.820 1 11-1-1 0 I I-F-1 7 10 M.T1.799 1 11-1-9 I I-F-31 M.T1.821 1 11-1- 1 0 Il-F-1 8 M.T1.800 1 11-1-9 Il-F-32 M.T1.822 1 11-1-1 0 Il-F-1 9 M.T1.801 1 11-1-9 I l-F-33 M.T1.823 1 11-1-1 0 I l-F-20 M.T1.802 1 11-1-9 I l-F-34 M.T1.824 1 11-1-1 0 I l-F- 21 15 M.T1.803 1 11-1-9 II-I-22 M.T1.825 1 11-1-1 0 I l-F-22 M.T1.804 1 11-1-1 0 I l-F-1 M.T1.826 1 11-1-1 0 I l-F-23 M.T1.805 1 11-1-1 0 I l-F-2 M.T1.827 1 11-1-1 0 I l-F-24 M. T1.806 1 11-1-1 0 I l-F-3 M.T1.828 1 11-1-1 0 I l-F-25 M.T1.807 1 11-1-1 0 I l-F-4 M.T1. 829 1 11-1-1 0 I l-F-26 20 M.T1.808 1 11-1-1 0 ll-F-5 M.T1.830 1 11-1-1 0 I l-F-27 M.T1. 809 1 11-1-1 0 I I-F-6 M.T1.831 1 11-1-1 0 I I-F-28 M.T1.810 1 11-1-1 0 I I-F-7 M.T1.832 1 11-1-1 0 I I-F-29 M.T1.811 1 11-1-1 0 I I-F-8 M.T1.833 1 11-1-1 0 I I-F-30 M.T1.812 1 11- 1-1 0 ll-F-9 M.T1.834 1 11-1-1 0 I l-F-31 M.T1.813 1 11-1-1 0 I l-F-1 0 M.T1.835 1 11- 1-10 Il-F-32 CQQCnn / l 7Π7 / Β / ΥΙΛΙ 113 Mix No. Comp. 1 comp. II Comp. III Mixture No. Comp. 1 comp. II Comp. III M.T1.836 1 11-1-1 0 I I-F-33 M.T1.858 1 11-1-1 1 I I-F-20 M.T1.837 1 11-1-1 0 I I-F-34 M .T1.859 1 11-1-1 1 I l-F-21 5 M.T1.838 1 11-1-1 0 II-I-22 M.T1.860 1 11-1-11 I l-F-22 M. T1.839 1 11-1-1 1 I I-F-1 M.T1.861 1 11-1-1 1 I I-F-23 M.T1.840 1 11-1-11 I I-F-2 M.T1.862 1 11-1-11 I I-F-24 M.T1.841 1 11-1-1 1 I I-F-3 M.T1.863 1 11-1-1 1 I I-F-25 M.T1.842 1 11- 1-11 I l-F-4 M.T1.864 1 11-1-11 I I-F-26 10 M.T1.843 1 11-1-11 ll-F-5 M.T1.865 1 11-1-11 I I-F-27 M.T1.844 1 11-1-1 1 I I-F-6 M.T1.866 1 11-1-1 1 I I-F-28 M.T1.845 1 11-1-11 ll-F -7 M.T1.867 1 11-1-11 I I-F-29 M.T1.846 1 11-1-1 1 I I-F-8 M.T1.868 1 11-1-1 1 I I-F-30 15 M.T1.847 1 11-1-11 I l-F-9 M.T1.869 1 11-1-11 ll-F-31 M.T1.848 1 11-1-11 I l-F-1 0 M.T1 .870 1 11-1-11 I I-F-32 M.T1.849 1 11-1-1 1 I I-F-11 M.T1.871 1 11-1-1 1 I I-F-33 M.T1.850 1 11-1-11 I I-F-1 2 M.T1.872 1 11-1-11 I I-F-34 M.T1.851 1 11-1-1 1 I I-F-1 3 M.T1.873 1 11- 1-1 1 II-I-22 20 M.T1.852 1 11-1-11 I I-F-1 4 M.T1.874 1 11-1-1 2 I I-F-1 M.T1.853 1 11- 1-1 1 Il-F-1 5 M.T1.875 1 11-1-1 2 Il-F-2 M.T1.854 1 11-1-11 Il-F-1 6 M.T1.876 1 11-1 -1 2 Il-F-3 M.T1.855 1 11-1-11 Il-F-1 7 M.T1.877 1 11-1-1 2 Il-F-4 M.T1.856 1 11-1-1 1 I l-F-1 8 M.T1 .878 1 11-1-1 2 ll-F-5 M.T1.857 1 11-1-11 I I-F-1 9 M.T1.879 1 11-1-1 2 Il-F-6 CQQCnn / l 7Π7 / Β / Υ Mix No. Comp. 1 comp. II Comp. III M.T1.880 1 11-1-1 2 I 1-F-7 M.T1.881 1 11-1-1 2 I 1-F-8 M.T1.882 1 11-1-1 2 ll-F-9 M.T1.883 1 11-1-1 2 I l-F-1 0 M.T1.884 1 11-1-1 2 ll-F-1 1 M.T1.885 1 11-1-1 2 ll-F -1 2 M.T1.886 1 11-1-1 2 I l-F-1 3 M.T1.887 1 11-1-1 2 I l-F-1 4 M.T1.888 1 11-1-1 2 ll -F-1 5 M.T1.889 1 11-1-1 2 ll-F-1 6 M.T1.890 1 11-1-1 2 ll-F-1 7 M.T1.891 1 11-1 -1 2 ll-F-1 8 M.T1.892 1 11-1-1 2 ll-F-1 9 M.T1.893 1 11-1-1 2 Il-F-20 M.T1.894 1 11 -1-1 2 I I-F-21 M.T1.895 1 11-1-1 2 I I-F-22 M.T1.896 1 11-1-1 2 I I-F-23 M.T1.897 1 11-1 -1 2 I I-F-24 M.T1.898 1 11-1-1 2 ll-F-25 M.T1.899 1 11-1-1 2 I I-F-26 M.T1.900 1 11-1- 1 2 Il-F-27 M.T1.901 1 11-1-1 2 ll-F-28 Mix No. Comp. 1 comp. II Comp. III M.T1 .902 1 11-1-1 2 I l-F-29 M.T1 .903 1 11-1-1 2 ll-F-30 M.T1.904 1 11-1-1 2 ll-F- 31 M.T1.905 1 11-1-1 2 I I-F-32 M.T1.906 1 11-1-1 2 I I-F-33 M.T1.907 1 11-1-1 2 I I-F-34 M .T1.908 1 11-1-1 2 II-I-22 M.T1.909 1 II-1-1 3 ll-F-1 M.T1.910 1 II-1-1 3 I-F-2 M .T1.91 1 1 11-1-1 3 I l-F-3 M.T1.912 1 11-1-1 3 I l-F-4 M.T1.913 1 11-1-1 3 ll-F-5 M .T1.914 1 II-1-1 3 I I-F-6 M.T1.915 1 11-1-1 3 I I-F-7 M.T1.916 1 11-1-1 3 I I-F-8 M.T1 .917 1 11-1-1 3 ll-F-9 M.T1.918 1 II-1-1 3 I l-F-1 0 M.T1.919 1 II-1-1 3 ll-F-1 1 M .T1.920 1 11-1-1 3 I l-F-1 2 M.T1.921 1 11-1-1 3 I l-F-13 M.T1 .922 1 11-1-1 3 I l-F-1 4 M .T1.923 1 II-1-1 3 Il-F-1 5 CQQCnn / l 7Π7 / Β / ΥΙΛΙ 115 Mix No. Comp. 1 comp. II Comp. III M.T1.924 1 11 - 1-13 ll-F-1 6 M.T1.925 1 11 - 1-13 ll-F-1 7 M.T1.926 1 11 - 1-13 ll-F- 1 8 M.T1.927 1 11 - 1-13 ll-F-1 9 M.T1.928 1 11 - 1-13 ll-F-20 M.T1.929 1 11 - 1-13 ll-F- 21 M.T1.930 1 11 - 1-13 I I-F-22 M.T1.931 1 11 - 1-13 I I-F-23 M.T1.932 1 11 - 1-13 I I-F-24 M.T1. 933 1 11 - 1-13 ll-F-25 M.T1.934 1 11 - 1-13 I 1-F-26 M.T1.935 1 11 - 1-13 I 1-F-27 M.T1.936 1 11 - 1-13 I I-F-28 M.T1.937 1 11 - 1-13 ll-F-29 M.T1.938 1 11 - 1-13 I I-F-30 M.T1.939 1 11 - 1-13 I I-F-31 M.T1.940 1 11 - 1-13 I I-F-32 M.T1.941 1 11 - 1-13 I I-F-33 M.T1.942 1 11 - 1-13 I I-F-34 M. T1.943 1 11 - 1-13 II-I-22 M.T1.944 1 11 - 1-14 ll-F-1 M.T1.945 1 11 - 1-14 I I-F-2 Mix No. Comp. 1 comp. II Comp. III M.T1 .946 1 II- 1-14 I l-F-3 M.T1 .947 1 II- 1-14 I l-F-4 M.T1.948 1 II- 1-14 I l-F-5 M.T1 . 949 1 II- 1-14 I 1-F-6 M.T1.950 1 II- 1-14 I 1-F-7 M.T1.951 1 II- 1-14 I 1-F-8 M.T1.952 1 II- 1 -14 I l-F-9 M.T1.953 1 II- 1-14 ll-F-10 M.T1.954 1 II- 1-14 ll-F-11 M.T1.955 1 II- 1-14 I l-F-1 2 M.T1.956 1 II- 1-14 I l-F-13 M.T1.957 1 II- 1-14 I l-F-1 4 M.T1.958 1 II- 1-14 I l-F-1 5 M.T1.959 1 II- 1-14 I l-F-1 6 M.T1.960 1 II- 1-14 I l-F-1 7 M.T1.961 1 II- 1-14 I l-F-1 8 M .T1.962 1 II- 1-14 I l-F-1 9 M.T1.963 1 II- 1-14 ll-F-20 M.T1.964 1 II- 1-14 ll-F-21 M.T1 .965 1 II- 1-14 I l-F-22 M.T1.966 1 II- 1-14 I l-F-23 M.T1.967 1 II- 1-14 I l-F-24 CQQCnn / l 7Π7 / Β / ΥΙΛΙ 116 Mix No. Comp. 1 comp. II Comp. III Mixture No. Comp. 1 comp. II Comp. III M.T1.968 1 11-1-1 4 I I-F-25 M.T1.990 1 11-1-1 5 I I-F-1 2 M.T1.969 1 11-1-1 4 I I-F-26 M.T1.991 1 11-1-1 5 I I-F-13 5 M.T1.970 1 11-1-1 4 I I-F-27 M.T1.992 1 11-1-1 5 I I-F-1 4 M.T1.971 1 11-1-1 4 I I-F-28 M.T1.993 1 11-1-1 5 I I-F-1 5 M.T1.972 1 11-1-1 4 I I-F-29 M .T1.994 1 11-1-1 5 I l-F-1 6 M.T1.973 1 11-1-1 4 I l-F-30 M.T1.995 1 11-1-1 5 I l-F-1 7 M .T1.974 1 11-1-1 4 I l-F-31 M.T1.996 1 11-1-1 5 I l-F-1 8 10 M.T1.975 1 11-1-1 4 I l-F-32 M .T1.997 1 11-1-1 5 I l-F-1 9 M.T1.976 1 11-1-1 4 I l-F-33 M.T1.998 1 11-1-1 5 I l-F-20 M. T1.977 1 11-1-1 4 I l-F-34 M.T1.999 1 11-1-1 5 I l-F-21 M.T1.978 1 11-1-1 4 II-I-22 M.T1 .1000 1 11-1-1 5 I I-F-22 15 M.T1.979 1 11-1-1 5 ll-F-1 M.T1.1001 1 11-1-1 5 I I-F-23 M.T1 .980 1 11-1-1 5 I I-F-2 M.T1.1002 1 11-1-1 5 I I-F-24 M.T1.981 1 11-1-1 5 I I-F-3 M.T1.1003 1 11-1-1 5 I I-F-25 M.T1.982 1 11-1-1 5 I I-F-4 M.T1.1004 1 11-1-1 5 I I-F-26 M.T1.983 1 11 -1-1 5 ll-F-5 M.T1.1005 1 11-1-1 5 I l-F-27 20 M.T1.984 1 11-1-1 5 I l-F-6 M.T1.1006 1 11 -1-1 5 I I-F-28 M.T1.985 1 11-1-1 5 ll-F-7 M.T1.1007 1 11-1-1 5 I I-F-29 M.T1.986 1 11- 1-1 5 I I-F-8 M.T1.1008 1 11-1-1 5 I I-F-30 M.T1.987 1 11-1-1 5 ll-F-9 M.T1.1009 1 11-1 -1 5 ll-F-31 M.T1.988 1 11-1-1 5 I l-F-1 0 M.T1.1010 1 11-1-1 5 I I-F-32 M.T1.989 1 11-1 -1 5 ll-F-1 1 M.T1.1011 1 11-1-1 5 Il-F-33 CQQCnn / l 7Π7 / Β / ΥΙΛΙ 117 Mix No. Comp. 1 comp. II Comp. III M.T1.1012 1 11 - 1-15 I 1-F-34 M.T1.1013 1 11 - 1-15 II-I-22 M.T1.1014 1 11 - 1-16 ll-F-1 M. T1.1015 1 11 - 1-16 I I-F-2 M.T1.1016 1 11 - 1-16 I I-F-3 M.T1.1017 1 11 - 1-16 I I-F-4 M.T1.1018 1 11 - 1-16 I I-F-5 M.T1.1019 1 11 - 1-16 I I-F-6 M.T1.1020 1 11 - 1-16 I I-F-7 M.T1.1021 1 11 - 1-16 I l-F-8 M.T1.1022 1 11 - 1-16 ll-F-9 M.T1.1023 1 11 - 1-16 I l-F-1 0 M.T1.1024 1 11 - 1-16 ll-F- 1 1 M.T1.1025 1 11 - 1-16 ll-F-1 2 M.T1.1026 1 11 - 1-16 I l-F-1 3 M.T1.1027 1 11 - 1-16 ll-F- 14 M.T1.1028 1 11 - 1-16 ll-F-1 5 M.T1.1029 1 11 - 1-16 ll-F-1 6 M.T1.1030 1 11 - 1-16 ll-F- 1 7 M.T1.1031 1 11 - 1-16 ll-F-1 8 M.T1.1032 1 11 - 1-16 ll-F-1 9 M.T1.1033 1 11 - 1-16 ll-F -twenty Mix No. Comp. 1 comp. II Comp. III M.T1.1034 1 II- 1-16 I l-F-21 M.T1.1035 1 II- 1-16 I l-F-22 M.T1.1036 1 II- 1-16 I l-F-23 M.T1. 1037 1 II- 1-16 I l-F-24 M.T1.1038 1 II- 1-16 ll-F-25 M.T1.1039 1 II- 1-16 I l-F-26 M.T1.1040 1 II- 1-16 I l-F-27 M.T1.1041 1 II- 1-16 I l-F-28 M.T1.1042 1 II- 1-16 ll-F-29 M.T1.1043 1 II- 1-16 I l-F-30 M.T1.1044 1 II- 1-16 ll-F-31 M.T1.1045 1 II- 1-16 I l-F-32 M.T1.1046 1 II- 1-16 I l-F-33 M .T1.1047 1 II- 1-16 I l-F-34 M.T1.1048 1 II- 1-16 II-I-22 M.T1.1049 1 II- 1-17 ll-F-1 M.T1. 1050 1 II- 1-17 I I-F-2 M.T1.1051 1 II- 1-17 I I-F-3 M.T1.1052 1 II- 1-17 I I-F-4 M.T1.1053 1 II- 1 -17 I l-F-5 M.T1.1054 1 II- 1-17 I l-F-6 M.T1.1055 1 II- 1-17 I l-F-7 CQQCnn / l 7Π7 / Β / ΥΙΛΙ 118 Mix No. Comp. 1 comp. II Comp. III M.T1.1056 1 11 - 1-17 ll-F-8 M.T1.1057 1 11 - 1-17 I 1-F-9 M.T1.1058 1 11 - 1-17 I 1-F-1 0 M. T1.1059 1 11 - 1-17 ll-F-1 1 M.T1.1060 1 11 - 1-17 ll-F-1 2 M.T1.1061 1 11 - 1-17 I 1-F-1 3 M. T1.1062 1 11 - 1-17 I l-F-1 4 M.T1.1063 1 11 - 1-17 ll-F-1 5 M.T1.1064 1 11 - 1-17 ll-F-1 6 M. T1.1065 1 11 - 1-17 ll-F-1 7 M.T1.1066 1 11 - 1-17 ll-F-1 8 M.T1.1067 1 11 - 1-17 ll-F-1 9 M .T1.1068 1 11 - 1-17 ll-F-20 M.T1.1069 1 11 - 1-17 I 1-F-21 M.T1.1070 1 11 - 1-17 I 1-F-22 M.T1.1071 1 11 - 1-17 I I-F-23 M.T1.1072 1 11 - 1-17 I I-F-24 M.T1.1073 1 11 - 1-17 I I-F-25 M.T1.1074 1 11 - 1- 17 I I-F-26 M.T1.1075 1 11 - 1-17 I I-F-27 M.T1.1076 1 11 - 1-17 I I-F-28 M.T1.1077 1 11 - 1-17 I I-F-29 Mix No. Comp. 1 comp. II Comp. III M.T1.1078 1 II- 1-17 ll-F-30 M.T1.1079 1 II- 1-17 I 1-F-31 M.T1.1080 1 II- 1-17 I 1-F-32 M.T1 .1081 1 II- 1-17 I l-F-33 M.T1.1082 1 II- 1-17 I l-F-34 M.T1.1083 1 II- 1-17 II-I-22 M.T1.1084 1 II - 1-18 ll-F-1 M.T1.1085 1 II- 1-18 I I-F-2 M.T1.1086 1 II- 1-18 I I-F-3 M.T1.1087 1 II- 1-18 I I-F-4 M.T1.1088 1 II- 1-18 I I-F-5 M.T1.1089 1 II- 1-18 I I-F-6 M.T1.1090 1 II- 1-18 I I-F-7 M .T1.1091 1 II- 1-18 ll-F-8 M.T1.1092 1 II- 1-18 I l-F-9 M.T1.1093 1 II- 1-18 I l-F-1 0 M.T1. 1094 1 II- 1-18 ll-F-11 M.T1.1095 1 II- 1-18 I l-F-1 2 M.T1.1096 1 II- 1-18 I l-F-13 M.T1.1097 1 II - 1-18 I l-F-1 4 M.T1.1098 1 II- 1-18 I l-F-1 5 M.T1.1099 1 II- 1-18 I l-F-1 6 CQQCnn / l 7Π7 / Β / Υ 119 Mix No. Comp. 1 comp. II Comp. III M.T1.1100 1 11 - 1-18 I I-F-1 7 M.T1.1 101 1 11 - 1-18 I I-F-1 8 M.T1.1102 1 11 - 1-18 I I-F-1 9 M.T1.1 103 1 11 - 1-18 I I-F-20 M.T1.1104 1 11 - 1-18 ll-F-21 M.T1.1105 1 11 - 1-18 I I-F-22 M.T1 .1106 1 11 - 1-18 I I-F-23 M.T1.1107 1 11 - 1-18 I I-F-24 M.T1.1108 1 11 - 1-18 I I-F-25 M.T1.1109 1 11 - 1-18 ll-F-26 M.T1.1110 1 11 - 1-18 I l-F-27 M.T1.1111 1 11 - 1-18 I l-F-28 M.T1.1112 1 11 - 1-18 I I-F-29 M.T1.1113 1 11 - 1-18 I I-F-30 M.T1.1114 1 11 - 1-18 ll-F-31 M.T1.1115 1 11 - 1-18 I I-F-32 M .T1.1116 1 11 - 1-18 I l-F-33 M.T1.1 117 1 11 - 1-18 I l-F-34 M.T1.1118 1 11 - 1-18 II-I-22 M.T1. 1119 1 11 - 1-19 I I-F-1 M.T1.1120 1 11 - 1-19 I I-F-2 M.T1.1121 1 11 - 1-19 I I-F-3 Mix No. Comp. 1 comp. II Comp. III M.T1 .1 122 1 II- 1-19 I l-F-4 M.T1 .1 123 1 II- 1-19 I l-F-5 M.T1.1124 1 II- 1-19 I l-F-6 M. T1 .1 125 1 II- 1-19 I l-F-7 M.T1.1126 1 II- 1-19 I l-F-8 M.T1 .1 127 1 II- 1-19 I l-F-9 M.T1.1128 1 II- 1-19 I l-F-1 0 M.T1.1129 1 II- 1-19 I l-F-11 M.T1.1130 1 II- 1-19 I l-F-1 2 M.T1.1131 1 II- 1-19 I l-F-13 M.T1.1132 1 II- 1-19 ll-F-14 M.T1.1133 1 II- 1-19 I l-F-1 5 M.T1.1134 1 II- 1-19 I l-F-1 6 M.T1.1135 1 II- 1-19 I l-F-1 7 M.T1.1136 1 II- 1-19 I l-F-1 8 M.T1.1137 1 II- 1-19 I l-F -1 9 M.T1.1138 1 II- 1-19 I l-F-20 M.T1.1139 1 II- 1-19 ll-F-21 M.T1.1140 1 II- 1-19 I l-F-22 M .T1.1141 1 II- 1-19 I l-F-23 M.T1 .1 142 1 II- 1-19 I l-F-24 M.T1.1143 1 II- 1-19 I l-F-25 120 Mix No. Comp. 1 comp. II Comp. III M.T1.1 144 1 11-1-1 9 I l-F-26 M.T1.1 145 1 11-1-1 9 I l-F-27 M.T1.1146 1 11-1-1 9 I l-F- 28 M.T1.1 147 1 11-1-1 9 I l-F-29 M.T1.1148 1 11-1-1 9 I l-F-30 M.T1.1 149 1 11-1-1 9 I l-F- 31 M.T1.1150 1 11-1-1 9 Il-F-32 M.T1.1151 1 11-1-1 9 Il-F-33 M.T1.1152 1 11-1-1 9 Il-F-34 M .T1.1153 1 11-1-1 9 II-I-22 M.T1.1154 1 II-I-20 I l-F-1 M.T1.1155 1 ​​II-I-20 I l-F-2 M.T1. 1156 1 II-I-20 I l-F-3 M.T1.1157 1 II-I-20 I l-F-4 M.T1.1158 1 II-I-20 I l-F-5 M.T1.1159 1 II-I -20 I l-F-6 M.T1.1160 1 II-I-20 I l-F-7 M.T1.1161 1 II-I-20 I l-F-8 M.T1.1162 1 II-I-20 I l-F- 9 M.T1.1163 1 II-I-20 I l-F-1 0 M.T1.1164 1 II-I-20 I l-F-11 M.T1.1165 1 II-I-20 I l-F-1 2 Mix comp. Comp. Comp. No. 1 II III M.T1 .1 166 1 11-1-20 I l-F-13 M.T1 .1 167 1 11-1-20 I l-F-1 4 M.T1.1168 1 11-1-20 I l-F-1 5 M.T1 .1 169 1 II-1-20 I l-F-1 6 M.T1.1170 1 11-1-20 I l-F-1 7 M.T1 .1 171 1 11-1-20 I l-F-1 8 M.T1.1172 1 11-1-20 I l-F-1 9 M.T1.1173 1 II-1-20 I l-F-20 M.T1.1174 1 II-1-20 I l-F- 21 M.T1.1175 1 11-1-20 I l-F-22 M.T1.1176 1 11-1-20 I l-F-23 M.T1.1177 1 11-1-20 I l-F-24 M.T1. 1178 1 II-1-20 I I-F-25 M.T1.1179 1 11-1-20 I I-F-26 M.T1.1180 1 11-1-20 I I-F-27 M.T1.1181 1 11-1 -20 I l-F-28 M.T1.1182 1 II-1-20 I l-F-29 M.T1.1183 1 II-1-20 I l-F-30 M.T1.1184 1 11-1-20 I l-F- 31 M.T1.1185 1 11-1-20 I I-F-32 M.T1 .1 186 1 11-1-20 I I-F-33 M.T1.1187 1 II-1-20 I I-F-34 CQQCnn / l 7Π7 / Β / Υ 121 Mix No. Comp. 1 comp. II Comp. III Mixture No. Comp. 1 comp. II Comp. III M.T1.1188 1 11-1-20 II-I-22 M.T1.1210 1 II-I-21 I l-F-22 M.T1.1 189 1 11-1-21 I l-F-1 M. T1.1211 1 II-I-21 I I-F-23 5 M.T1.1190 1 11-1-21 I I-F-2 M.T1.1212 1 II-I-21 I I-F-24 M.T1.1191 1 11-1-21 I I-F-3 M.T1.1213 1 11-1-21 I I-F-25 M.T1.1192 1 11-1-21 I I-F-4 M.T1.1214 1 II-I-21 I I-F-26 M.T1.1193 1 11-1-21 ll-F-5 M.T1.1215 1 II-I-21 I I-F-27 M.T1.1194 1 11-1-21 I I-F-6 M.T1.1216 1 II-I-21 I I-F-28 10 M.T1.1195 1 11-1-21 ll-F-7 M.T1.1217 1 11-1-21 I I-F-29 M.T1 .1196 1 11-1-21 I l-F-8 M.T1.1218 1 11-1-21 ll-F-30 M.T1.1197 1 11-1-21 ll-F-9 M.T1.1219 1 II-I-21 ll-F-31 M.T1.1198 1 11-1-21 ll-F-10 M.T1.1220 1 II-I-21 I-F-32 M.T1.1199 1 11-1 -21 I I-F-11 M.T1.1221 1 II-I-21 I I-F-33 1 0 M.T1.1200 1 11-1-21 I I-F-1 2 M.T1.1222 1 11-1-21 I l-F-34 M.T1.1201 1 11-1-21 I l-F-1 3 M.T1.1223 1 II-I-21 II-I-22 M.T1.1202 1 11-1-21 I l-F- 1 4 M.T1.1203 1 11-1-21 I l-F-1 5 M.T1.1224 1 11-1-1 II-I-2 M.T1.1204 1 11-1-21 I l-F-1 6 M.T1.1225 1 11-1-1 II-I-3 20 M.T1.1205 1 11-1-21 I l-F-1 7 M.T1.1226 1 11-1-1 II-I-4 M .T1.1206 1 11-1-21 I l-F-1 8 M.T1.1227 1 11-1-1 II-I-5 M.T1.1207 1 11-1-21 I l-F-1 9 M.T1 .1228 1 11-1-1 II-I-6 M.T1.1208 1 11-1-21 I l-F-20 M.T1.1229 1 11-1-1 II-I-7 M.T1.1209 1 11-1-21 I l-F-21 M.T1.1230 1 11-1-1 II-I-8 122 Mix No. Comp. 1 comp. II Comp. III Mixture No. Comp. 1 comp. II Comp. III M.T1.1231 1 11-1-1 11-1-9 M.T1.1253 1 11-1-1 2 11-1-1 4 M.T1.1232 1 11-1-1 11-1- 1 0 M.T1.1254 1 11-1-1 2 11-1-1 5 5 M.T1.1233 1 11-1-1 11-1-11 M.T1.1255 1 11-1-1 2 11 -1-1 6 M.T1.1234 1 11-1-1 11-1-1 2 M.T1.1256 1 11-1-1 2 11-1-1 7 M.T1.1235 1 11-1- 1 11-1-1 3 M.T1.1257 1 11-1-1 2 11-1-1 8 M.T1.1236 1 11-1-1 11-1-1 4 M.T1.1258 1 11- 1-1 2 11-1-1 9 M.T1.1237 1 11-1-1 11-1-1 5 M.T1.1259 1 11-1-1 2 II-I-20 10 M.T1.1238 1 11-1-1 11-1-1 6 M.T1.1260 1 11-1-1 2 II-I-21 M.T1.1239 1 11-1-1 11-1-1 7 M.T1. 1261 1 11-1-1 2 II-I-2 M.T1.1240 1 11-1-1 11-1-1 8 M.T1.1262 1 11-1-1 2 II-I-3 M.T1 .1241 1 11-1-1 11-1-1 9 M.T1.1263 1 11-1-1 2 II-I-4 15 M.T1.1242 1 11-1-1 II-I-20 M. T1.1264 1 11-1-1 2 II-I-5 M.T1.1243 1 11-1-1 11-1-21 M.T1.1265 1 11-1-1 2 II-I-6 M. T1.1244 1 11-1-1 2 11-1-2 M.T1.1266 1 11-1-1 2 II-I-7 M.T1.1245 1 11-1-1 2 11-1-3 M .T1.1267 1 11-1-1 2 II-I-8 M.T1.1246 1 11-1-1 2 11-1-4 M.T1.1268 1 11-1-1 2 II-I-9 20 M.T1.1247 1 11-1-1 2 11-1-5 M.T1.1269 1 11-1-1 2 11-1-1 0 M.T1.1248 1 11-1-1 2 11- 1-6 M.T1.1270 1 11-1-1 2 11-1-1 4 M.T1.1249 1 11-1-1 2 11-1-7 M.T1.1271 1 11-1-1 2 11-1-1 5 M.T1.1250 1 11-1-1 2 11-1-8 M.T1.1272 1 11-1-1 2 11-1-1 6 M.T1.1251 1 11-1 -1 2 11-1-9 M.T1.1273 1 11-1-1 2 11-1-1 7 M.T1.1252 1 11-1-1 2 11-1-1 0 M.T1.1274 1 11-1-1 2 11-1-1 8 CQQCnn / l 7Π7 / Β / Υ 123 Mix No. Comp. 1 comp. II Comp. III M.T1.1275 1 11 - 1-12 11-1-1 9 M.T1.1276 1 11 - 1-12 II-I-20 M.T1.1277 1 11 - 1-12 11-1-21 M.T1.1278 1 11 - 1-13 11-1-2 M.T1.1279 1 11 - 1-13 11-1-3 M.T1.1280 1 11 - 1-13 11-1-4 M. T1.1281 1 11 - 1-13 11-1-5 M.T1.1282 1 11 - 1-13 11-1-6 M.T1.1283 1 11 - 1-13 11-1-7 M.T1. 1284 1 11 - 1-13 11-1-8 M.T1.1285 1 11 - 1-13 11-1-9 M.T1.1286 1 11 - 1-13 11-1-10 M.T1.1287 1 11 - 1-13 11-1-1 4 M.T1.1288 1 11 - 1-13 11-1-1 5 M.T1.1289 1 11 - 1-13 11-1-1 6 M.T1.1290 1 11 - 1-13 11-1-1 7 M.T1.1291 1 11 - 1-13 11-1-1 8 M.T1.1292 1 11 - 1-13 11-1-1 9 M.T1. 1293 1 11 - 1-13 II-I-20 M.T1.1294 1 11 - 1-13 11-1-21 M.T1.1295 1 11 - I-2 11-1-8 M.T1.1296 1 11 - I-2 11-1-9 Mix No. Comp. 1 comp. II Comp. III M.T1.1297 1 11-1-2 11-1-1 0 M.T1.1298 1 11-1-2 11-1-1 4 M.T1.1299 1 11-1-2 11-1- 1 5 M.T1.1300 1 II-1-2 11-1-1 6 M.T1.1301 1 11-1-2 11-1-1 7 M.T1.1302 1 11-1-2 11-1 -1 9 M.T1.1303 1 11-1-2 II-I-20 M.T1.1304 1 II-1-2 II-I-8 M.T1.1305 1 II-1-2 II-I- 9 M.T1.1306 1 11-1-2 11-1-1 0 M.T1.1307 1 11-1-2 11-1-1 4 M.T1.1308 1 11-1-2 11-1- 1 5 M.T1.1309 1 II-1-2 11-1-1 6 M.T1.1310 1 11-1-2 11-1-1 7 M.T1.1311 1 11-1-2 11-1 -1 9 M.T1.1312 1 11-1-2 II-I-20 M.T1.1313 1 II-1-3 II-I-8 M.T1.1314 1 II-1-3 II-I- 9 M.T1.1315 1 11-1-3 11-1-1 0 M.T1.1316 1 11-1-3 11-1-1 4 M.T1.1317 1 11-1-3 11-1- 1 5 M.T1.1318 1 II-1-3 11-1-1 6 CQQcnn / ι ζηζ / Ε / γ 124 Mix No. Comp. 1 comp. II Comp. III M.T1.1319 1 11 - 1-3 11-1-1 7 M.T1.1320 1 11 - 1-3 11-1-1 9 M.T1.1321 1 11 - 1-3 II-I- 20 M.T1.1322 1 11 - 1-4 11-1-8 M.T1.1323 1 11 - 1-4 11-1-9 M.T1.1324 1 11 - 1-4 11-1-1 0 M.T1.1325 1 11 - 1-4 11-1-1 4 M.T1.1326 1 11 - 1-4 11-1-1 5 M.T1.1327 1 11 - 1-4 11-1-1 6 M.T1.1328 1 11 - 1-4 11-1-1 7 M.T1.1329 1 11 - 1-4 11-1-1 9 M.T1.1330 1 11 - 1-4 II-I- 20 M.T1.1331 1 11 - 1-5 11-1-8 M.T1.1332 1 11 - 1-5 11-1-9 M.T1.1333 1 11 - 1-5 11-1-1 0 M.T1.1334 1 11 - 1-5 11-1-1 4 M.T1.1335 1 11 - 1-5 11-1-1 5 M.T1.1336 1 11 - 1-5 11-1-1 6 M.T1.1337 1 11 - 1-5 11-1-1 7 M.T1.1338 1 11 - 1-5 11-1-1 9 M.T1.1339 1 11 - 1-5 II-I- 20 M.T1.1340 1 11 - 1-5 11-1-8 Mix No. Comp. 1 comp. II Comp. III M.T1.1341 1 11-1-5 11-1-9 M.T1.1342 1 11-1-5 11-1-1 0 M.T1.1343 1 11-1-5 11-1-1 4 M.T1.1344 1 II-1-5 11-1-1 5 M.T1.1345 1 11-1-5 11-1-1 6 M.T1.1346 1 11-1-5 11-1- 1 7 M.T1.1347 1 11-1-5 11-1-1 9 M.T1.1348 1 II-1-5 II-I-20 M.T1.1349 1 II-1-6 II-I- 8 M.T1.1350 1 11-1-6 II-I-9 M.T1.1351 1 11-1-6 11-1-1 0 M.T1.1352 1 11-1-6 11-1-1 4 M.T1.1353 1 II-1-6 11-1-1 5 M.T1.1354 1 11-1-6 11-1-1 6 M.T1.1355 1 11-1-6 11-1- 1 7 M.T1.1356 1 11-1-6 11-1-1 9 M.T1.1357 1 II-1-6 II-I-20 M.T1.1358 1 II-1-7 II-I- 8 M.T1.1359 1 11-1-7 II-I-9 M.T1.1360 1 11-1-7 11-1-1 0 M.T1.1361 1 11-1-7 11-1-1 4 M.T1.1362 1 II-1-7 11-1-1 5 CQQCnn / l 7Π7 / Β / Υ 125 Mix No. Comp. 1 comp. II Comp. III M.T1.1363 1 11 - 1-7 11-1-1 6 M.T1.1364 1 11 - 1-7 11-1-1 7 M.T1.1365 1 11 - 1-7 11-1- 1 9 M.T1.1366 1 11 - 1-7 II-I-20 M.T1.1367 1 11 - 1-21 11-1-8 M.T1.1368 1 11 - 1-21 11-1-9 M.T1.1369 1 11 - 1-21 11-1-1 0 M.T1.1370 1 11 - 1-21 11-1-1 4 M.T1.1371 1 11 - 1-21 11-1-1 5 M.T1.1372 1 11 - 1-21 11-1-1 6 M.T1.1373 1 11 - 1-21 11-1-1 7 M.T1.1374 1 11 - 1-21 11-1- 1 9 M.T1.1375 1 11 - 1-21 II-I-20 M.T1.1376 1 11 - 1-18 11-1-8 M.T1.1377 1 11 - 1-18 11-1-9 M.T1.1378 1 11 - 1-18 11-1-1 0 M.T1.1379 1 11 - 1-18 11-1-1 4 M.T1.1380 1 11 - 1-18 11-1-1 5 M.T1.1381 1 11 - 1-18 11-1-1 6 M.T1.1382 1 11 - 1-18 11-1-1 7 M.T1.1383 1 11 - 1-18 11-1- 1 9 M.T1.1384 1 11 - 1-18 II-I-20 Mix No. Comp. 1 comp. II Comp. III M.T1.1385 1 II- 1-16 II-I-8 M.T1.1386 1 II- 1-16 II-I-9 M.T1.1387 1 II- 1-16 11-1-1 0 M.T1.1388 1 II- 1-16 11-1-1 4 M.T1.1389 1 II- 1-16 11-1-1 5 M.T1.1390 ​​1 II- 1-16 11-1-1 7 M.T1.1391 1 II- 1-16 11-1-1 9 M.T1.1392 1 II- 1-16 II-I-20 M.T1.1393 1 II- 1-15 II-I-8 M.T1.1394 1 II- 1-15 II-I-9 M.T1.1395 1 II- 1-15 11-1-1 0 M.T1.1396 1 II- 1-15 11-1-1 4 M.T1.1397 1 II- 1-15 11-1-1 7 M.T1.1398 1 II- 1-15 11-1-1 9 M.T1.1399 1 II- 1-15 II-I-20 M.T1.1400 1 II- I-8 II-I-9 M.T1.1401 1 II- I-8 11-1-1 0 M.T1.1402 1 II- I-8 11-1-1 4 M.T1.1403 1 II- I-8 II-I-20 M.T1.1404 1 II- 1-19 II-I-9 M.T1.1405 1 II- 1-19 11-1-1 0 M .T1.1406 1 II- 1-19 11-1-1 4 CQQcnn / ι ζηζ / Ε / γ 126 Mix No. Comp. 1 comp. II Comp. III M.T1.1407 1 11-1-1 9 II-I-20 M.T1.1408 1 11-1-1 7 11-1-9 M.T1.1409 1 11-1-1 7 11-1 -1 0 M.T1.1410 1 11-1-1 7 11-1-1 4 Mix No. Comp. 1 comp. II Comp. III M.T1.1411 1 11-1-1 7 II-I-20 M.T1.1412 1 11-1-1 0 II-I-9 M.T1.1413 1 11-1-1 0 11-1 -1 4 M.T1.1414 1 11-1-1 0 II-I-20 CQQCnn / l 7Π7 / Β / ΥΙΛΙ As mentioned above, the mixtures according to the present invention may comprise the compound of Formula (I) combined with 1, 2, 3 or 4 additional active ingredients. Therefore, the mixtures that were described in Table T-1 above may additionally comprise one or two additional active ingredients, selected from fungicides or insecticides. According to one embodiment, the user can mix the 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 premixed components, for example components comprising the compounds I and / or active substances from groups M.1 to M.Y or F.l) to F.XII) listed above, in a spray tank, and other auxiliaries and additives may be added, 127 to be suitable. In another embodiment, the individual components of the composition according to the invention or the partially premixed components, for example components comprising compounds I and / or active substances from groups M.1 to M.Y or F.l) to F.X11) listed above, can be applied together (for example, after tank mix) or consecutively. Biological examples Biological tests The ap I icabi I i ty of the compounds of Formula (I) separately or in combination with other active ingredients in application methods according to the present invention can be evaluated in test examples as provided herein below. or in similar trials. These examples should not be construed as limiting. As mentioned above, mixtures of the compound of Formula (I) with other agriculturally acceptable active ingredients can show surprisingly synergistic effects, which can also be demonstrated in the biological test systems described below. 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 of the compounds. The presence of a synergistic effect, in terms of percent control, between two mix components (X and Y) can be calculated using Colby's equation (Colby, S. R., 1967, Calculating Synergistic and Antagonistic CQQCnn / l 7Π7 / Β / ΥΙΛΙ 128 Responses in Herbicide Combinations, Weeds, 15, 20-22): E = X + Y- — 100 When the effect of the combined control observed is greater than the effect of the combined control expected (E), then the combined effect is synergistic. Analysis of synergy or antagonism between the mixtures or compositions was determined by Colby's equation. B.1 Control of animal pests With regard to the control of animal pests affecting plant propagation material, especially seeds, the following test systems and results show the pesticidal activity of the carboxamide compound of Formula I separately and its synergistic pesticidal activity in combination with other insecticidal active ingredients. Test B.1.1 Control of wireworm (Melanotus communis) To evaluate wireworm (Melanotus communis) control by direct contact methods, individual insects were directly immersed in a solution of the compound. Compounds or mixtures were dissolved in acetone at different concentrations. Compounds or mixtures were formulated using a solution containing 50% (v / v) acetone in water with 0.02% by weight of Kinetic®. For the experimental mixtures, identical volumes of both mixture components were mixed together to achieve the CQQCnn / l 7Π7 / Β / ΥΙΛΙ 129 desired respective concentrations. Wireworms were directly immersed in a solution for three seconds, and then air-dried on filter paper. About 11 cm3 of water-moistened clayey sand was placed in each 16-cm2 cell of the 32-cell rear tray. One treated wireworm larva was infested in each cell along with two sprouting wheat seeds. The cells were then covered with adhesive bioassay tray lids. Each cell was a replicate, and replication was performed 10x. After infestation, the test was kept in an incubator at 26 ± 1 °C in the dark. Mortality (dead + dying insects) was evaluated 3 days after treatment (DAT), and the average percentage mortality was calculated with respect to the untreated control. The results are listed in Table B.1.1. Table B.1.1: CQQCnn / l 7Π7 / Ε / Υ Melanotus communis concentration [ppm] % of average control Test B.1.1 a): Carboxamide compound of Formula I 3 33 C ian t ran i I i p r o I 225 22 Cyantraniliprole + Carboxamide compound of Formula 225+3 78* 130 Melanotus communis concentration [ppm] % control average Formula I Test B.1.1 .b) Carboxamide compound of Formula I 3 33 Emamectin 800 11 Emamectin + Carboxamide compound of Formula I 800+3 44* Test B.1.1 . c) Carboxamide compound of Formula I 3 33 Fipronil 30 22 Fipronil + Carboxamide compound of Formula I 30+3 89* CQQcnn / ι ζηζ / Ε / γ 131 Melanotus communis concentration [PPm] % of average control Test B.1.1 .d) Formula I carboxamide compound 3 33 Thiamethoxam 25 11 Thiamethoxam + Formula I carboxamide compound 25+3 44* *effect of synergistic control according to Colby's equation Test B.1.2 Control of Western Corn Rootworm (Diabrotica virgifera virgitera) To evaluate western corn rootworm (Diabrotica virgifera virgifera) control by a maximum exposure method, insects were exposed to treated soil. The compounds or mixtures were first dissolved in acetone, and then mixed with the soil to obtain the different concentrations (w / w) desired in ppm of compound / soil or mixture / soil. For experimental mixtures, identical volumes of both mixture components were mixed together to achieve the desired respective concentrations. Treatments were applied in solution to sieved clayey sand (#10 sieve) in a plastic bag. Treatments were intensively incorporated by sealing and shaking each 132 bag by hand, allowing the solution to permeate through the soil mass for at least 10 minutes. The bags were then opened and left open in a fume hood overnight to evaporate the solvent from the soil. One day after treatment (DAT) water for wetting and a water-soaked millet seed as a food source were added to each bag and thoroughly incorporated. About 11 cm3 of the millet-soil mixture was placed in a 1-oz plastic cup. Each cup was infested with 10 second stage western corn rootworm larvae and covered. Each cup was a replicate, and replication was performed 3x. The test was kept in an incubator at 26 ± 1 °C in the dark. Mortality (dead + dying insects) was evaluated 3 days after infestation (DAI), and the average percentage mortality was calculated with respect to the untreated control. The results are listed in Table B.1.2. CQQCnn / l 7Π7 / Β / Υ Table B.1.2: Diabrotica virgifera virgifera concentration [ppm of compound or mixture / soil] % of average control Test B.1,2.a) Carboxamide compound of Formula I 0.01 30 Clotian id ín 0.1 33 133 Diabrotica virgifera virgifera concentration [ppm of compound or mixture / soil] % of average control Clothianidin + Carboxamide compound of Formula I 0.1+0.01 70* Test B.1.2.b) Carboxamide compound of Formula I 0 .01 30 Ciantran i I ¡pro I 3.1 23 Ciantran iliprole + Carboxamide compound of Formula I 3.1+0.01 50* Test B.1.2.c) Carboxamide compound of Formula I 0, 01 30 Fipronil 0.03 27 Fipronil + Carboxamide Compound 0.03 + 0.01 63* CQQCnn / l 7Π7 / Β / Υ 134 Diabrotica virgifera virgifera concentration [ppm of compound or mixture / soil] % of average control Formula I Test B.1,2.d) Carboxamide compound of Formula I 0.01 30 Imidacloprid 0.13 17 Imidacloprid + Carboxamide compound of Formula I 0.13 + 0.01 63* Test B.1.2.e) Carboxamide compound of Formula I 0.01 30 Thiacloprid 0.2 37 Thiacloprid + Carboxamide compound of Formula I 0.2 + 0.01 70* *effect of synergistic control according to Colby's equation Test B.1.3 Control of black cutworm (Agrotis ipsilon) To evaluate the control of the black cutworm (Agrotis ipsilon) CQQcnn / ι ζηζ / Ε / γ 135 using a direct contact method, individual insects were directly immersed in a solution of the compound. Compounds or mixtures were dissolved in acetone at different concentrations. Compounds or mixtures were formulated using a solution containing 50% (v / v) acetone in water with 0.02% by weight of Kinetic®. For experimental mixtures, identical volumes of both mixture components were mixed together to achieve the desired respective concentrations. Second stage black cutworms were directly immersed in a solution for three seconds, and then air-dried on filter paper. One treated black cutworm larva was infested in each 16-cm2 cell of the 32-cell rear tray along with removed shoots from a corn plant and a moistened cotton wick. The cells were then covered with adhesive bioassay tray lids. Each cell was a replicate, and replication was performed 16x. After infestation, the test was kept in an incubator at 25.5 ± 15C and a 14l:10D light cycle. Mortality (dead + dying insects) was evaluated 1 and 5 days after treatment (DAT), and the average percentage mortality was calculated with respect to the untreated control. The results are listed in Table B.1.3. CQQCnn / l 7Π7 / Β / Υ 136 CQQcnn / ι ζηζ / Ε / γ Table B.1.3: Agrotis Ípsilon concentration [PPm] % of average control 1 DAT % of average control 5 DAT Test B.1,3.a) Carboxamide compound of Formula I 3 38 44 Fipronil 300 13 31 Fipronil + v 300+3 81* 81 * *effect of synergistic control according to Colby's equation Test B.1.4 Control of maize seed larvae (Delia platera) To evaluate the control of the corn seed larva (Delia platera) by maximum exposure, the insects were exposed to the treated soil. The compounds or mixtures were first dissolved in acetone, and then mixed with the soil to obtain the different concentrations (w / w) desired in ppm of compound / soil or mixture / soil. For experimental mixtures, identical volumes of both mixture components were mixed together to achieve the desired respective concentrations. Treatments were applied in solution to sieved dry play sand (#10 sieve) in a glass jar. Treatments were thoroughly incorporated by capping and shaking each vial by hand, allowing the solution to permeate through 137 the mass of sand for at least 10 minutes. The jars were then uncapped, and the sand was kept in a fume hood for 4 hours to evaporate the solvent. After the hood was dried, 10 cm3 of treated sand was placed in a 1-oz plastic cup. with bone meal in the background as a food source. Each cup was moistened with 4 mL of water, infested with five second-stage seedcorn larvae, and covered. Each cup was a replicate, and replication was performed 5x. The test was kept in an incubator at 22 ± 1 °C in the dark. Mortality (dead + dying insects) was evaluated 2 days after treatment (DAT), and the average percentage mortality was calculated with respect to the untreated control. The results are listed in Table B.1.4. CQQCnn / l 7Π7 / Β / Υ Table B.1.4 Delia platura concentration [ppm of compound or mixture / soil] % of average control Test B.1,4.a) Carboxamide compound of Formula I 0.06 21 Cyan tran i I i pr o I 10 64 Cyantraniliprole + 10+ 0.06 96* 138 Delia platura concentration [ppm of compound or mixture / soil] % of average control Carboxamide compound of Formula I Test B.1,4.b) V 0.06 21 Imidacloprid 3 18 Imidacloprid + Carboxamide compound of Formula I 3 + 0.06 52* *effect of synergistic control according to Colby's equation CQQcnn / ι ζηζ / Ε / γ Test B.1.5 Control of root-knot nematodes (Meloidogyne spp.) To evaluate control of root-knot nematodes (Meloidogyne spp.) by exposure via drench application, the nematodes were introduced into treated cucumber plants. Compounds or mixtures were dissolved in acetone at different concentrations. Compounds or mixtures were formulated using a solution containing 50% (v / v) acetone in water with 0.02% by weight of Kinetic®. For experimental mixtures, they were mixed Mix 139 identical volumes of both components together to achieve the desired respective concentrations. Sprouted cucumber seeds were planted in 1 oz black plastic cups (one seed per cup) with sieved dry play sand (#10 sieve). Treatments were applied as a drench in 7 mL of solution to each cup, which was held in a fume hood for 1 hour to allow acetone to evaporate. The cups were transferred to an environmental chamber (25 ± 2 °C, 24 I) and watered daily during the test. Each cup was a replicate, and replication was performed 5x. In the cotyledonous stage of cucumber, each cup was infested with 500 juvenile root-knot nematodes (J2s) in 1 ml of distilled water. Four weeks after infestation, the cucumber roots were washed, and the galls and clutch volume were counted. The control was calculated as the reduction in galls or spawn volume with respect to the untreated control. The mean percentage control was calculated for each treatment. The results are listed in Table B.1.5. CQQCnn / l 7Π7 / Β / Υ 140 Table B.1.5: CQQCnn / l 7Π7 / Β / Υ Delia platura concentration [mg of compound or mixture / plant] % control of average galls % control of average spawn volume Test B.1.5.a) Carboxamide compound of Formula I 0.3 35 -21 Abamectin 0.017 40 39 Abamectin + Carboxamide Compound of Formula I 0.017+0.3 99* 100* Test B.1.5.b) Carboxamide Compound of Formula I 0.3 35 -21 Abamectin 0.008 24 17 141 Delia platura concentration [mg of compound or mixture / plant] % control of average galls % control of average spawn volume Abamectin + Carboxamide Compound of Formula I 0.008+0.3 100* 99* *effect of synergistic control according to Colby's equation CQQCnn / l 7Π7 / Β / ΥΙΛΙ Other examples of tests with which the control of pests that infest soils can be evaluated are described below. BP.1.1 Tests for spider mites (Tetranychus) Test BP.1.2 Soil drench test on lima beans The test solution comprising a compound of the present invention was prepared in the desired concentration with water and an organic solvent. Potted lima bean plants were treated with the test solution by drenching the soil. Test compounds were applied as a soil drench in 2 ml of solution at a rate of 4 mg active ingredient / plant (2 mg / ml). The technical material was dissolved in acetone, and then water was distilled to achieve a final concentration of 5% acetone. Four days after treatment, a mixed population of spider mites (Tetranychus 142 urticae) of two spots on the leaves. After infestation, the plants were kept on a cart in the laboratory and watered daily from the top. Five days after the release of the spider mites, the acaricidal efficacy was measured with means of scoring the damage caused by the spider mites or the mortality of the spider mites: the amount of TSSM on the plants was counted; the percentage of damage as lesions was evaluated visually, and the means were calculated for each treatment. The average percent population reduction relative to the solvent blank control was calculated. The average percentage of damage reduction with respect to the solvent blank was calculated as 100-(average % of lesions in the treatment / average % of lesions in solvent blank)*1 00. Test BP.1.3 Seed treatment trial on cotton The test solution comprising a compound of the present invention was prepared in the desired concentration with water and an organic solvent. Cottonseeds were coated with the test solution prepared at a rate of 0.5 mg active ingredient / seed and sown into the pots. After the plants emerged, a mixed population of two-spotted spider mites was released on the leaves. Four days after the release of the spider mites, the acaricidal efficacy was measured by scoring means of mite damage or spider mite mortality: the percentage of damage as lesions was evaluated visually, and the means were calculated for each treatment. . The average percentage reduction in damage from the CQQCnn / l 7Π7 / Β / Υ 143 solvent blank was calculated as 100-(average % lesions in treatment / average % lesions in solvent blank)*1 00. Test BP.1.4 Test of seed treatment on cucumber The test solution comprising a compound of the present invention was prepared in the desired concentration with water and acetone as an organic solvent. Cucumber seeds were coated with the prepared test solution applied at a rate of 0.5 mg active ingredient / seed and sown in the pots. After plant emergence (eleven days after treatment and planting), a mixed population of two-spotted spider mites was released onto the leaves. Four days after the release of the spider mites, the acaricidal efficacy was measured by scoring the damage caused by the spider mites. The percentage of damage as lesions was evaluated visually, and the means for each treatment were calculated. The average percentage reduction in damage with respect to the solvent blank was calculated as 100-(Average % lesions in treatment / Average % lesions in solvent blank)*1 00. BP.1.5 Tests for nematodes (Meloidogyne) Test B.2.1 Soil drench on tomato against juvenile root-knot nematodes Tomatoes were grown in potting soil to approximately the first true leaf stage (about 2 weeks after planting). The tomatoes were transplanted into CQQCnn / l 7Π7 / Β / Υ 144 arena for play. Seven days after transplantation, the test compound technical material was dissolved in acetone, and then water was added to reach a final concentration of 50% acetone. 1 ml of solution was pipetted onto the root zone of the tomato. One day after treatment (DAT), each pot was infested with about 500 juvenile root-knot nematodes (Meliodogyne spp.) in 1 ml of distilled water. Immediately after infestation, the plants were placed in the greenhouse. Plants were watered from the top and fertilized daily. Fourteen DAT, the tomato roots were rinsed, and the number of galls counted. Replication was performed 5 times. B.2 Control of phytopathogenic fungi Regarding the control of phytopathogenic fungi that affect plant propagation material, especially seeds, the following test systems and results show the fungicidal activity of the carboxamide compound of Formula I separately and its synergistic fungicidal activity in combination with other fungicidal active ingredients. Microassays for the evaluation of fungicidal activity The active compounds were formulated separately as a stock solution having a concentration of 10,000 ppm in dimethyl sulfoxide. B.2.1. Activity against the rice fungus Pyricularia oryzae Stock solutions were mixed according to the indicated ratio, pipetted into a microtiter plate. CQQCnn / l 7Π7 / Β / Υ 145 (MTP) and diluted with water to the indicated concentrations. Then, a suspension of Pyricularia oryzae spores in an aqueous solution of biomalt or yeast-bactopeptone-glycerin was added. The plates were placed in a chamber saturated with water vapor at a temperature of 18 °C. With an absorption photometer, MTPs were measured at 405 nm, 7 days after inoculation. The results are listed in Table B.2.1 below. CQQcnn / ι ζηζ / Ε / γ Table B.2.1. : Pyricularia oryzae Active compound / Active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) carboxamide compound of Formula I 16 4 1 0.063 - 4 15 12 2 Epoxiconazole 0.25 0.063 28 1 carboxamide compound of Formula I Epoxiconazole 16 0.25 64:1 100 31 69 146 Active compound / Active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Calculated efficacy according to Colby (%) Synergy (%) carboxamide compound of Formula I 4 63:1 100 15 85 Epoxiconazole 0.063 carboxamide compound of Formula I 4 16:1 100 39 61 Epoxiconazole 0.25 carboxamide compound of Formula I Epoxiconazole 1 0.063 16:1 100 13 87 B.2.2. Activity against early blight caused by Alternaria solani Stock solutions were mixed according to the indicated ratio, pipetted into a microtiter plate (MTP) and diluted with water to the indicated concentrations. Then, a suspension of Alternaria solani spores in an aqueous solution of biomalt or yeast-bactopeptonaglycerin was added. The plates were placed in a chamber saturated with steam. CQQCnn / l 7Π7 / Β / Υ 147 water at a temperature of 18 °C. With an absorption photometer, MTPs were measured at 405 nm, 7 days after inoculation. The results are reported in Table B.2.2 below. CQQCnn / l 7Π7 / Β / Υ Table B.2.2.: Alternaria cassock Active Compound / Active Compounds in Mixture Concentration (ppm) Mixture (Ratio) Observed Efficacy Calculated Efficacy according to Colby (%) Synergy (%) Carboxamide Compound of Formula I 63 16 4 1 - 0 0 0 0 Pyraclostrobin 0.063 0.016 12 0 T riticonazole 1 0.25 23 0 carboxamide compound of Formula I Pyraclostrobin 16 0.063 254:1 36 12 24 carboxamide compound of Formula I 63 1000:1 40 12 28 148 Active Compound / Active Compounds in Mixture Concentration (PPm) Mixture (Ratio) Observed Efficacy Calculated Efficacy according to Colby (%) Synergy (%) Formula I Pyraclostrobin 0.063 carboxamide compound of Formula I 63 4000:1 24 0 24 Pyraclostrobin 0.016 carboxamide compound of Formula I T riticonazole 63 1 63:1 43 23 20 carboxamide compound of Formula I T riticonazole 16 0.25 64:1 32 0 32 carboxamide compound of Formula I T riticonazole 4 0.25 16: 1 20 0 20 composed of 4 4:1 52 23 29 CQQcnn / ι ζηζ / Ε / γ 149 Active compound / Active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Efficacy calculated according to Colby (%) Synergy (%) carboxamide of Formula I T riticonazole 1 carboxamide compound of Formula I 1 4:1 34 0 34 T riticonazole 0.25 CQQCnn / l 7Π7 / Β / Υ B.2.3. Activity against Microdochium nivale Stock solutions were mixed according to the indicated ratio, pipetted into a microtiter plate (MTP) and diluted with water to the indicated concentrations. Then, a suspension of Microdochium nivale spores in an aqueous solution of biomalt or yeast-bactopeptonaglycerin was added. The plates were placed in a chamber saturated with water vapor at a temperature of 18 °C. With an absorption photometer, MTPs were measured at 405 nm, 7 days after inoculation. The results are reported in Table B.2.3 below. 150 Table B.2.3.: Microdochium nivale Active compound / Active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Efficacy calculated according to Colby (%) Synergy (%) carboxamide compound of Formula I 63 16 - 4 15 4 - 13 Pyraclostrobin 0.016 - 46 Fluxapyroxad 0.063 0.004 0 0 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 composed of 63 4000:1 93 48 45 151 Active Compound / Active Compounds in Mixture Concentration (ppm) Mixture (Ratio) Observed Efficacy Calculated Efficacy according to Colby (%) Synergy (%) carboxamide of Formula I pyraclostrobin 0.016 carboxamide compound of Formula I fluxapyroxad 63 0.063 1000 :1 35 4 31 carboxamide compound of Formula I fluxapyroxad 63 0.004 16000:1 25 4 21 carboxamide compound of Formula I 4 250:1 63 38 25 Epoxiconazole 0.016 carboxamide compound of Formula I Epoxiconazole 63 0.016 4000:1 99 31 68 152 Active compound / Active compounds in the mixture Concentration (PPm) Mixture (ratio) Observed efficacy Efficacy calculated according to Colby (%) Synergy (%) carboxamide compound of Formula I 16 4000:1 99 21 78 Epoxiconazole 0.004 CQQCnn / l 7Π7 / Β / ΥΙΛΙ B.2.4. Activity against Rhizoctonia solani Stock solutions were mixed according to the indicated ratio, pipetted into a microtiter plate (MTP) and diluted with water to the indicated concentrations. Then, a suspension of Rhizoctonia solani spores in an aqueous solution of biomalt or yeast-bactopeptonaglycerin was added. The plates were placed in a chamber saturated with water vapor at a temperature of 18 °C. With an absorption photometer, MTPs were measured at 405 nm, 7 days after inoculation. The results are reported in Table B.2.4 below. 153 Table B.2.4.: Rhizoctonia solani CQQCnn / l 7Π7 / Β / ΥΙΛΙ 5 10 15 20 Active Compound / Active Compounds in Mixture Concentration (ppm) Mixture (Ratio) Observed Efficacy Efficacy Calculated According to Colby (%) Synergy (%) Carboxamide Compound of Formula I: 16 4 1 - 0 0 0 Epoxiconazole 0.016 - 24 0.004 0.001 - 0 0 T riticonazole 0.25 - 41 carboxamide compound of Formula I Epoxiconazole 4 0.016 250:1 55 24 31 carboxamide compound of Formula I 63 4000:1 96 31 65 Epoxiconazole 0.0 16 compound of carboxamide of Formula I 16 4000:1 75 0 75 154 Active compound / Active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Efficacy calculated according to Colby (%) Synergy (%) Epoxiconazole 0.004 carboxamide compound of Formula I 4 4000:1 20 0 20 Epoxiconazole 0.001 carboxamide compound of Formula I Epoxiconazole 1 0.016 63:1 44 24 20 carboxamide compound of Formula I T riticonazole 16 0.25 64:1 67 41 26 carboxamide compound of Formula I T riticonazole 4 0.25 16:1 67 41 26 carboxamide compound of 1 4:1 69 41 28 CQQCnn / l 7Π7 / Β / Υ 155 Active compound / Active compounds in the mixture Concentration (ppm) Mixture (ratio) Observed efficacy Efficacy calculated according to Colby (%) Synergy (%) Formula I T riticonazole 0.25 The measured parameters were compared with the growth of the control variant free of active compound (100%) and with the blank value free of fungi and free of active compound to determine the relative growth in % of the pathogens on the respective active compounds. . These percentages were converted to efficiencies. As mentioned above, the predicted efficacies of the active compound mixtures were determined by the Colby formula [R.S. Colby, “Calculating synergistic and antagonistic responses of herbicide combinations, Weeds 15, 20-22 (1967)] and compared with observed efficacies.

Claims

CLAIMS 1. Use of an active carboxamide compound as a pesticide of Formula (I): CQQCnn / l 7P7 / B / YILI or tautomers, enantiomers, diastereomers or salts thereof, wherein the active compound I of Formula (I) is combined and / or applied together with at least one other active compound in agriculture selected from the group of insecticides and / or fungicides consisting of thiophanate-methyl, acetate, triflumezopyrim, bifenthrin, cypermethrin, prothioconazole, tebuconazole, thiabendazole, etiprol, cyclaniliprol, spirotetramate, spiromesifen, spirodiclofen, thioxafen, teflubenzuron, flufenoxuron, lufenuron, chlorfenapyr, 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1 (1,2,4-triazolo-1yl)pentan-2-ol, 1 - [4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1 cyclopropyl-2(1,2,4-triazol-1-yl)ethanol, 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1 (1,2,4-tr iazol -1 -yl)butan-2-ol, 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1 -(1,2,4triazol-1 -yl)butan-2-ol,2-[4-(4-chlorophenoxy)-2-(trifluoromet¡l)phen¡l]-3-methyl1 - (1,2,4-triazol-1 - yl)butan-2-ol, 2-[4-(4-chlorophenox¡)-2(trifluoromethyl)phenyl]-1-(1,2,2,4-I-I yl)propan-2-ol, 2-[2-el oro-4-(4chlorophenoxy)phenyl]-3-methyl-1 - (1,2,4-triazol-1 -yl)butan-2-ol, 2-[4-(4chlorophenoxy)-2-(trifluoromet¡l)phenyl]-1-1 (1,2,4-triazol-1-yl)pentan-2-ol o 2-[4(4-fluorophenoxy)-2-(trifluoromethyl)phenyl]-1 - (1,2,4-triazol-1 - yl)propan-2-ol, N[4,6-dichloro-2-[(d¡et¡l-lambda-4-sulfan¡l¡den)carbamoyl]-phen¡l]-2-(3-chloro157 2-pyr¡dyl)-5-(tr¡fluoromethyl)pyrazol-3-carboxam¡da, N-[4-chloro-2-[(diethylambda-4-sulfanylden)carbamo¡l]-6-met¡l-phen¡l]-2-[3-chloro-2-p¡r¡d¡l)-5(trifluoromethyl)p¡razol-3-carboxam¡da o N-[4-chloro-2-[(di-2-propyl-lambda4-sulfanyl¡den)carbamo¡l]-6-met¡l-phen¡l]-2-(3-chloro-2-p¡r¡dyl)-5(trifluoromethyl)p¡razol-3-carboxam¡da and an active signature and control bacilli animal pests in soil application methods and seed treatment methods,wherein the active compound of Formula (I) is applied directly and / or indirectly to the plant and / or plant propagation material by soaking the soil, applying drip irrigation to the soil, injecting the soil, dipping, or treating seeds.

2. Use according to claim 1, wherein at least one additional agriculturally active compound selected from the group of insecticides and / or fungicides is combined and / or applied with it.

3. Use according to claim 2, wherein the at least one additional active compound is the fungicide pyraclostrobin.

4. Use according to claim 2, wherein the at least one additional active compound is the fungicide metalaxyl.

5. Use according to claim 1 or 2, wherein the other or at least one additional active compound is the fungicide thiophanate-methyl.

6. Use according to claim 1 or 2, wherein the other or at least one additional active compound is selected from the group comprising 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1 (1,2,4-triazol-1 -yl)pentan2-ol, 1-[4-(4-chlorophenoxy)-2-(trifluoromet¡l)phen¡l]-1 cyclopropyl-2-( 1,2,4triazol-1 - i I) ethane and 1, 2-[4-(4-chlorophenoxy)-2-(trifluorometh¡l)phen¡l)-Ql-Ql-Ql-Cl 7Π7 / Β / ΥΙΛΙ 158 triazol-1 -yl)butan-2-ol, 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1 -(1,2,4-triazol-1yl)butan-2-ol, 2-[4-(4-chlorophenoxy¡)-2-(tr¡fluoromethyl)phen¡l]-3-meth¡l-1-(1,2,4triazol-1 - yl)butan-2-ol, 2-[4-(4-chlorophenoxy)-2-(tr¡fluoromethyl)-1,1,2-triazol]-1 -yl)propan-2-ol, 2-[2-chloro-4-(4-chlorophenoxy)phen¡l]-3-met¡l-1 (1,2,4-triazol-1 -yl)butan-2-ol, 2-[4-(4-chlorophenox¡)-2-(tr¡fluoromethyl)-phen¡ol-1,4-1,1 -yl)pentan-2-ol o 2-[4-(4-fluorophenox¡)-2(trifluoromethyl)phenyl]-1-(1,2,4-tr i az o I-1 - yl)propan-2-ol.

7. Use according to claim 2, wherein at least one additional active compound is an insecticide selected from the group consisting of acephate, chlorpyrifos, fipronil, methiocarb, thiodicarb, lambda-cyhalothrin, cypermethrin, alpha-cypermethrin, bifenthrin, tefluthrin, acetamiprid, clothianidin, dinotefuran, imidacloprid, thiacloprid, thiamethoxam, abamectin, emamectin, flubendiamide, chlorantranil iprole, chlorantranil iprole, triflumezopyrim, spinosad, sulfoxaflor, or actives based on Bacillus firmus or P. nishizawae.

8. Use according to claim 2, wherein the at least one additional active compound is the fungicide fluxapyroxad.

9. Use according to claim 2, wherein the other at least one additional third active compound is the insecticide thiamethoxam.

10. Use according to claim 2, wherein the other active compound is Votivo® (Bacillus firmus strain 1-1582).

11. Use of the active carboxamide compound as a pesticide of Formula (I) in combination with at least one other active ingredient according to any of claims 1 to 10, wherein the plant or plant propagation material to be treated is grown in an artificial growth substrate.

12. Use of the active carboxamide compound as a pesticide of Formula (I) according to claim 11, wherein the artificial growth substrate is selected from rock wool, glass wool, quartz sand, gravel, expanded clay, and vermiculite.

13. Use of the active carboxamide compound as a pesticide of Formula (I) in combination with at least one other active ingredient according to any of claims 1 to 10, wherein the plant or plant propagation material to be treated is planted or grown in a closed system.

14. A method for protecting plant propagation material comprising contacting the plant propagation material with the combination of compounds as defined in any of claims 1 to 10, in quantities effective as pesticides, wherein the plant propagation material is transgenic plant seeds.

15. Seed comprising at least two active compounds as defined in any of claims 1 to 10 in an amount of 0.1 g / 10 kg per 100 kg of seeds.