ES2812779T3 - Compositions containing cis-jasmone and Bacillus amyloliquefaciens - Google Patents

Abstract

Pesticide mixtures comprising, as active components, Bacillus amyloliquefaciens ssp. plantarum strain MBI600 and cis-jasmone in synergistically effective amounts, where the ratio of Bacillus amyloliquefaciens ssp. The plantarum strain MBI600 a cis-jasmone is 1016 CFU: 1 g to 105 CFU: 1 g.

Description

DESCRIPTION

Compositions containing cis-jasmone and Bacillus amyloliquefaciens

The invention relates to pesticidal mixtures comprising, as active components, Bacillus amyloliquefaciens ssp. plantarum strain MBI600 (component A) and cis-jasmone (component B) in synergistically effective amounts, where the proportion of Bacillus amyloliquefaciens ssp., plantarum strain MBI600 to cis-jasmone is 1016 CFU: 1 g to 105 CFU: 1 g . It further relates to methods for controlling pests, which method comprises the application of pesticide mixtures to plants, plant propagation material or the place of growth of the plants; pests or their food supply, habitat or breeding grounds. It also refers to plant propagation material comprising pesticide mixtures.

Invertebrate pests and, in particular, insects, arachnids and nematodes destroy growing and harvested crops, thus causing great economic loss to food supply and property. Regulatory requirements, pesticide resistance, reduced application rates and toxicity, as well as increased applicant safety are just some of the innovation-driving issues that trigger the search for improved agrochemicals. Pesticide mixtures are favorably used to combat pests, because they convey the benefit of reduced resistance induction and a range of application against a broader spectrum of pests. In case the pesticides act synergistically, the application rates can be reduced. Consequently, there is a continuing need for pesticide mixtures to combat pests that address the above problems and objectives.

In this regard, it is noted that selected row crops of wheat, corn, barley, oats, rye, rice, soybeans, cotton, sugar beet, rapeseed and potato, which are of particular commercial importance, are highly vulnerable in terms of attack. or infestation by certain pests of invertebrates and harmful phytopathogenic fungi. Invertebrate pests relevant to above row crops include aphids, diptera, grasshoppers, triplets, nematodes, and whiteflies. Consequently, a mixture of pesticides is required, which has pesticidal activity against the above-mentioned pests. Therefore, an object of the present invention is to provide pesticide mixtures, which are suitable for protecting a selected plant of wheat, corn, barley, oats, rye, rice, soybean, cotton, sugar beet, rapeseed and potato against the effects harmful from the pests mentioned above.

In addition, there is a desire for pesticide mixtures that improve "plant health" as defined below. Therefore, another object of the invention is to provide pesticide mixtures that are suitable for improving plant health.

In relation to the above objects, it is emphasized that, in certain situations, in particular the seeds and the roots and shoots of plants are threatened by harmful pests. Accordingly, there also exists a continuing need for pesticide mixtures and seed treatment compositions comprising such pesticide mixtures, which are suitable for protecting plant propagation material, in particular seeds, and plant roots and shoots. from attack and infestation by harmful pests. It is particularly desired to provide pesticide mixtures and seed treatment compositions, which not only have activity against pests in the soil, which threaten the seeds and roots of the plant, but also ensure protection against foliar pests, when They are applied only to the seeds, for example by seed covering, seed coating, seed spraying, seed soaking or seed granulation, to protect plant shoots. Therefore, another object of the present invention is to provide pesticide mixtures and seed treatment compositions, which are suitable for protecting plant propagation material, in particular the seeds and roots and shoots of a plant, against harmful effects of pests. In particular, it is an object to provide mixtures of pesticides and seed treatment compositions, which are suitable for protecting the shoots of a plant.

Pests that are particularly relevant to crop plants are nematodes, which are among the most damaging pests for crop plants above. Because most of them live in the soil, they represent one of the most difficult pest problems to identify, demonstrate and control. It has been estimated that about 10 percent of world crop production is lost as a result of damage caused by plant nematodes (Whitehead, Plant nematode control, 1998). Economically relevant species are, among others, cereal cyst nematodes (Heterodera spp.), Root lesion nematodes (Pratylenchus spp.), Potato cyst nematodes (Globodera sp.), Root knot nematodes (Meloidogyne spp. .), seed gall nematodes (Anguina tritici) and stem nematodes (Ditylenchus spp.). Typically, these nematodes infest the roots of the crop plant or feed on plant propagation material, such as seeds, that has been distributed.

The above problems and objectives were successfully addressed by pesticidal mixtures of Bacillus amyloliquefaciens and cis-jasmone in synergistically effective amounts; and by methods of applying pesticide mixtures, in particular against nematodes. The advantages of the inventive subject matter are a synergistic effect of pesticide mixtures, in particular against nematodes, a reduced application rate, higher selectivities for certain pests, a reduced toxicity to humans and a safer application and handling. of the pesticide mixtures. In addition, the pesticide mixtures can be mixed with other pesticides in seed treatment compositions, such as insecticides and / or fungicides, to act synergistically or to act against a broader range of pests.

Document WO 2015/177021 refers to mixtures that comprise, as active components, Bacillus strains AP-136, AP-188, APP-218, AP-219, AP-295, AP-209 and / or AP-217 and a pesticide.

WO 2011/117272 relates to cis-jasmone mixtures and methods for using the mixtures in the field of agriculture. However, mixtures comprising cis-jasmone and strains of the genus Bacillus are not disclosed.

US 2015/289516 refers to the control of plant parasitic nematodes and a composition comprising Bacillus amyloliquefaciens strain FZB42 and at least one other nematicide in a synergistically effective amount. However, mixtures comprising cis-jasmone are not disclosed.

Cis-jasmone is a natural organic product derived from plants. Cis-jasmone (IUPAC name 1-methyl-3-methylene-2 - [(Z) -pent-2-enyl] cyclopentene) is a commercially available compound of formula A:

Several strains of the genus Bacillus associated with plants belonging to the species Bacillus amyloliquefaciens or Bacillus subtilis have been described. They are used commercially to promote growth and improve the health of crop plants (Phytopathology 96, 145-154, 2006). Recently, the Bacillus subtilis MBI600 strain has been reclassified as Bacillus amyloliquefaciens ssp. plantarum MBI600 based on polyphasic tests that combines classical microbiological methods that are based on a mixture of traditional tools (such as culture-based methods) and molecular tools (such as genotype and fatty acid analysis). Therefore, Bacillus subtilis MBI600 (or MBi 600 or MBI-600) is identical to Bacillus amyloliquefaciens ssp. plantarum MB1600, formerly Bacillus subtilis MBI600. For the purpose of this invention, Bacillus subitilis MBI600 will mean Bacillus amyloliquefaciens ssp. plantarum MBI600, formerly Bacillus subtilis MBI600.

Bacillus amyloliquefaciens ssp. plantarum MBI600 (component A) is deposited with the American Type Culture Collection (AtcC) under Safe Deposit Number SD-1414. In addition, it has accession number NRRL B-50595 and was deposited with the United States Department of Agriculture on November 10, 2011 under the strain designation Bacillus subtilis 1430. It was also deposited with The National Collections of Industrial and Marine Bacteria Ltd. (NCIB), Torry Research Station, PO Box 31, 135 Abbey Road, Aberdeen, AB9 8DG, Scotland under accession number 1237 on December 22, 1986.

MBI600 is known as a rice seed treatment that promotes plant growth, according to Int. J. Microbiol. Res. ISSN 0975-5276, 3 (2) (2011), 120-130 and is further described, for example, in US 2012/0149571 A1. This MBI600 strain is commercially available as the Integral® liquid formulation product (BASF Corp., USA).

Bacillus amyloliquefaciens and / or Bacillus subtilis are naturally occurring spore-forming bacteria found, for example, in soils or on plant surfaces throughout the world. Bacillus subtilis strain MBI600 was isolated from a broad bean plant leaf surface grown at Nottingham University School of Agriculture, Sutton Bonington, UK. Bacillus subtilis MBI600 was grown using art-known fermentation techniques and media, for example, in tryptic soy broth (TSB) at 27 ° C for 24-72 hours. Bacterial cells (vegetative cells and spores) can be washed and concentrated (eg, by centrifugation at room temperature for 15 minutes at 7000 xg). To produce a dry formulation, bacterial cells, preferably spores, were suspended in a suitable dry vehicle (eg, clay). To produce a liquid formulation, the cells, preferably spores, were resuspended in a suitable liquid vehicle (eg, water-based) at the desired spore density. The number of spore density in spores per ml was determined by identifying the number of heat resistant colony forming units (70 ° C for 10 min) on soybean trypticase agar after incubation for 18-24 hours at 37 ° C.

Bacillus subtilis MBI600 is active at temperatures between 7 ° C and 52 ° C (Holtmann, G. and Bremer, E. (2004), J. Bacteriol. 186, 1683-1693).

The species Bacillus amyloliquefaciens, before 1987 known as a subspecies of Bacillus subtilis, comprises several subspecies that are commercially available or accessible as follows: Bacillus amyloliquefaciens strain AP-188 (NRRL 0-50615 and 0-50331; US 8,445,255) ; B. amyloliquefaciens ssp. plantarum D747 isolated from air at Kikugawashi, Japan (US20130236522 A1; FERM BP-8234; eg Double Nickel ™ 55 WDG from Certis LLC, USA), B. amyloliquefaciens ssp. plantarum FZB24 isolated from the soil in Brandenburg, Germany (also called SB3615; DSM 96-2; J. Plant Dis. Prot. 105, 181-197, 1998; eg, Taegro® from Novozyme Biologicals, Inc., USA), B. amyloliquefaciens ssp. plantarum FZB42 isolated from soil in Brandenburg, Germany (DSM 23117; J. Plant Dis. Prot. 105, 181-197, 1998; eg RhizoVital® 42 from AbiTEP GmbH, Germany), B. amyloliquefaciens ssp. plantarum strain MBI600 isolated from broad bean at Sutton Bonington, Nottinghamshire, UK at least before 1988 (available from the American Type Culture Collection (ATCC) under Safe Deposit Number SD-1414; also called 1430; NRRL O-50595; US 2012 / 0149571 A1; for example, Integral® from BASF Corp., USA), B. amyloliquefaciens ssp. plantarum QST-713 isolated from the 1995 peach orchard in California, USA (NrRl 0-21661; for example, Serenade® MAX from Bayer Crop Science LP, USA), B. amyloliquefaciens ssp. plantarum TJ1000 isolated in 1992 from South Dakota, United States (also referred to as 1 bE; ATCC BAN-390; CA 2471555 A1; for example, QuickRoots ™ from TJ Technologies, Watertown, SD, United States), B. subtilis FB17 also referred to as UD 1022 or UD10-22 isolated from red beet roots in North America (ATCC PTA-11857; System. Appl. Microbiol. 27, 372-379, 2004; US 2010/0260735; WO 2011/109395).

The term Bacillus amyloliquefaciens encompasses the species Bacillus amyloliquefaciens (including all subspecies, strains, and mutants thereof) and related bacteria within the genus Bacillus, for example, species, subspecies, strains, and mutants thereof, which have a genomic sequence that has at least 60%, preferably at least 80%, more preferably at least 85%, especially preferably at least 95% and in particular at least 99% sequence identity with the Bacillus amyloliquefaciens genome sequence (for example, with a of the strains in Table A). Sequence identity refers to the percentage of the same aligned DNA sequence bases. A suitable computer tool to determine the sequence identity of genomes is Wise2DBA offered by EMBL. The term "mutants" refers to bacteria that have at least 1 single nucleotide exchange, deletion or insertion, preferably at least 5, and in particular at least 10. In some cases, the mutants are related to transgenic bacteria. Transgenic bacteria carry at least one gene from a different species, or a derivative thereof (eg, a truncation, fusion, or mutation). Said mutants can be obtained by treatment with a chemical agent, such as N-methyl-N'-nitro-N-nitrosoguanidine, ethylmethanesulfone, or by irradiation using gamma rays, X-rays or UV radiation, or by other means well known to those skilled in the art. The matter. Mutants can also be obtained by selecting spontaneous mutants (such as phage resistant mutants) from a population of cells.

The particular microorganisms and strains described herein, unless specifically stated otherwise, are separated from nature and grown under artificial conditions, such as in cultures or by scale-up manufacturing processes, such as fermentation, described in this document. According to one embodiment of the present invention, the term Bacillus amyloliquefaciens refers not only to the pure and isolated cultures of the respective microorganisms, but also to their suspensions in a complete culture broth. Whole broth culture refers to a liquid culture that contains cells and media. The compositions of the present invention can be obtained by cultivating Bacillus amyloliquefaciens according to methods well known in the art. Conventional large-scale microbial culture processes include submerged fermentation, solid state fermentation, or liquid surface culture. Towards the end of fermentation, as nutrients are depleted, Bacillus cells begin the transition from the growth phase to the sporulation phase, so that the end product of fermentation is largely spores, metabolites, and residual fermentation medium. Fermentation is configured to obtain high levels of Bacillus colony-forming units and to promote sporulation. Bacterial cells, spores in the culture media resulting from fermentation can be used directly or concentrated by centrifugation, tangential flow filtration, deep filtration and evaporation. In some embodiments, the concentrated fermentation broth is washed, for example, by a diafiltration process, to remove residual fermentation broth and metabolites. The fermentation broth or broth concentrate can also be dried with or without the addition of carriers using conventional drying processes or methods such as spray drying, lyophilization, tray drying, fluid bed drying, drum drying or evaporation. Fermentation broth, broth concentrate and dry products are referred to herein as fermentation products. The pesticidal mixtures of the present invention may include fermentation products of Bacillus amyloliquefaciens ssp. plantarum strain MBI600. The term "in synergistically effective amounts" refers to a range of proportions of Bacillus amyloliquefaciens and cis-jasmone where both compounds act synergistically in the fight against pests. One way to measure the synergistic effect is by comparing the effect of the individual compounds with the combined effect of the mixed compounds according to Colby's formula given below.

The pesticidal mixtures of the invention comprise, as active components, Bacillus amyloliquefaciens ssp. plantarum strain MBI600 and cis-jasmone in synergistically effective amounts.

In another embodiment, the pesticidal mixture consists, as active components, of Bacillus amyloliquefaciens ssp. plantarum strain MBI600 and cis-jasmone in synergistically effective amounts.

In both cases, the ratio of Bacillus amyloliquefaciens to cis-jasmone is 1016 CFU: 1 g to 105 CFU: 1 g. In another embodiment, the ratio of Bacillus amyloliquefaciens to cis-jasmone is 1015 CFU: 1 g to 108 CFU: 1 g. In yet another embodiment, the ratio of Bacillus amyloliquefaciens to cis-jasmone is 1013 CFU: 1 g to 109 CFU: 1 g.

In yet another embodiment, the ratio of Bacillus amyloliquefaciens to cis-jasmone is 1013 CFU: 1 g to 1010 CFU: 1 g. In yet another embodiment, the ratio of Bacillus amyloliquefaciens to cis-jasmone is 5-1012 CFU: 1 g to 1010 CFU: 1 g. In yet another embodiment, the ratio of Bacillus amyloliquefaciens to cis-jasmone is 1011 CFU: 1 g. Colony Forming Unit (CFU) is a measure of viable microbial cells, particularly fungal and bacterial cells.

In one embodiment, the proportion of Bacillus amyloliquefaciens ssp. plantarum strain MBI600 to cis-jasmone is from 1015CFU: 1g to 108 CFU: 1g.

The ratio of Bacillus amyloliquefaciens to cis-jasmone can also be expressed as a weight ratio. The total weight ratios can be determined using the amount of u Fc of Bacillus amyloliquefaciens to calculate the total weight of the respective active component with the following equation that 1 x 1010 CFU is equal to one gram of total weight of the respective active component. Therefore, the weight ratio of Bacillus amyloliquefaciens to cis-jasmone is usually 106:10 to 1: 100,000. In yet another embodiment, the ratio of Bacillus amyloliquefaciens to cis-jasmone is 100,000: 1 to 1: 100. In yet another embodiment, the ratio of Bacillus amyloliquefaciens to cisjasmone is from 1000: 1 to 1:10. In yet another embodiment, the ratio of Bacillus amyloliquefaciens to cis-jasmone is 1000: 1 to 1: 1. In yet another embodiment, the ratio of Bacillus amyloliquefaciens to cis-jasmone is 500: 1 to 1: 1.

The pesticidal mixtures and / or compositions may also contain a component C. In another embodiment, the pesticidal mixtures and / or compositions comprise at least one component C. Component C can be selected from insecticides, nematicides and miticides, fungicides, herbicides, plant growth and the like. Preferred C components are insecticides, nematicides, and fungicides. Mixing a component C to pesticidal mixtures can also result in a synergistic effect of component C with Bacillus amyloliquefaciens, or cis-jasmone, or with Bacillus amyloliquefaciens and cis-jasmone. An additional advantage is a wider application range, lower application rates and higher selectivity. Pesticidal mixtures comprising component C are advantageously used in application methods, and are also preferably comprised in the plant propagation material of the present invention. Combinations of more than one component C are also suitable.

The following list M of pesticides, grouped and numbered according to the Mode of Action Classification of the Insecticide Resistance Action Committee (IRAC), together with which the pesticide mixtures of the present invention can be used and with which possible possible synergistic effects. produced, is intended to illustrate the possible combinations, but not to impose any limitation.

M.1 Acetylcholine esterase (AChE) inhibitors of the class of: M.1A carbamates, for example aldicarb, alanicarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, ethiophencarb, fenobucarb, furathiocarb, formethancarb, formethanecarb isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur, thiodicarb, thiophanox, trimetacarb, XMC, xylylcarb and triazamate; or of the class of: M.1B organophosphates, for example acephate, azamethiphos, azinphos-ethyl, azinphosmethyl, cadusafos, chlorethoxyphos, chlorfenvinphos, chloromephos, chlorpyrifos, chlorpyrifos-methyl, coumaphos, cyanophos, demeton-S-methyl, diazinon, dichlorophos / DDVP, dicrotophos, dimethoate, dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, famfur, fenamiphos, fenitrothion, fenthion, phostiazate, heptenophos, imitiaphos, isophenphos, isopropyl O- (methoxyamine-phosphoryl), methomidoscarbion, malathiophosphoryl , metidation, mevinphos, monochotophos, naled, omethoate, oxydemeton-methyl, parathion, parathion-methyl, phentoate, phorate, fosalone, phosmet, phosphamidon, poxim, pyrimiphos-methyl, profenophos, propetamphos, protiophos, pyraclphos, pyridaphosphention , tebupirimphos, temephos, terbufos, tetrachlorvinphos, thiometon, triazophos, trichlorfon and vamidothion;

M.2 GABN-activated chloride channel antagonists such as: M.2A organochlorine cyclodiene compounds, such as endosulfan or chlordane; or M.2B fiproles (phenylpyrazoles), such as ethiprole, fipronil, flufiprole, pyrafluprole and pyriprole;

M.3 Sodium channel modulators of the M.3A pyrethroid class, for example acrinathrin, allethrin, dcis-trans allethrin, d-trans allethrin, bifenthrin, bioalethrin, bioalethrin S-cyclopentenyl, bioresmethrin, cycloprothrin, cyfluthrin, beta- cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin, deltamethrin, empenthrin, phenofenvalethrin, fluitvarinato, phenprophenthrine, fluitvarinato, phenprophenthrin, fluitvalerate, fluvalinate, halfenprox, heptafluthrin, imiprothrin, meperfluthrin, metofluthrin, momfluorothrin, permethrin, phenothrin, pralethrin, profluthrin, pyrethrum (pyrethrum), resmethrin, silafluofen, tefluthrin, tetramethylfluthrin, tetralmethylfluthrin; or M.3B sodium channel modulators such as DDT or methoxychlor;

M.4 Nicotinic acetylcholine receptor (nAChR) agonists of the class of neonicotinoids M.4A, for example acetamiprid, clothianidin, cycloxaprid, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam; or the compounds M.4A.2: (2E -) - 1 - [(6-Chloropyridin-3-yl) methyl] -N'-nitro-2-pentylidenehydrazinecarboximidamide; or M4.A.3: 1 - [(6-chloropyridin-3-yl) methyl] -7-methyl-8-nitro-5-propoxy-1,2,3,5,6,7-hexahydroimidazo [1, 2-a] pyridine; or class M.4B nicotine;

M.5 Allosteric activators of the nicotinic acetylcholine receptor of the spinosyn class, eg, spinosad or spinetoram;

M.6 Chloride channel activators of the avermectin and milbemycin class, for example, abamectin, emamectin benzoate, ivermectin, lepimectin or milbemectin;

M.7 Juvenile hormone mimics, such as M.7A juvenile hormone analogs such as hydroprene, kinoprene, and methoprene; or others like M.7B fenoxycarb or M.7C or pyriproxyphene;

M.8 various non-specific (multisite) inhibitors, for example, M.8A alkyl halides such as methyl bromide and other alkyl halides, or M.8B chloropicrin, or M.8C sulfuryl fluoride, or M.8D borax, or M.8E tartar emetic; M.9 Selective homopteran feeding blockers, eg, M.9B pymetrozine, or M.9C flonicamid; M.10 Mite growth inhibitors, for example M.10A clofentezine, hexythiazox and diflovidazine, or M.10B ethoxazole;

M.11 Microbial disruptors of the intestinal membranes of the insect, for example, Bacillus thuringiensis or Bacillus sphaericus and the insecticidal proteins that 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: Cry1Ab, Cry1Ac, Cry1Fa, Cry2Ab, mCry3A, Cry3Ab, Cry3Bb and Cry34 / 35Ab1;

M.12 Mitochondrial ATP synthase inhibitors, eg, M.12A diafentiuron, or M.12B organotin miticides such as azocyclotin, cyhexatin or fenbutatin oxide, or M.12C propargite, or M.12D tetradiphon;

M.13 Oxidative phosphorylation decouplers through proton gradient disruption, eg chlorfenapir, DNOC, or sulfluramide;

M.14 Nicotinic acetylcholine receptor (nAChR) channel blockers, eg, nereistoxin analogs such as bensultap, cartap hydrochloride, thiocyclam, or thiosultap sodium;

M.15 Type 0 chitin biosynthesis inhibitors, such as benzoylureas such as bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron; or triflumuron;

M.16 Type 1 chitin biosynthesis inhibitors, such as buprofezin;

M.17 Molting disruptors, Dipteran, such as chromazine;

M.18 Ecdyson receptor agonists such as diacylhydrazines, eg, methoxyphenozide, tebufenozide, halofenozide, fufenozide or chromafenozide;

M.19 Octopamine receptor agonists, such as amitraz;

M.20 Inhibitors of electron transport of mitochondrial complex III, for example M.20A hydramethylnon, or M.20B acequinocyl, or M.20C fluacripirim;

M.21 Inhibitors of electron transport of mitochondrial complex I, for example M.21A METI acaricides and insecticides such as fenazaquin, fenpyroximate, pyrimidifene, pyridaben, tebufenpyrad or tolfenpyrad, or M.21B rotenone; M.22 Voltage-gated sodium channel blockers, for example M.22A indoxacarb, or M.22B metaflumizone, or M.22B.1: 2- [2- (4-Cyanophenyl) -1- [3- (trifluoromethyl ) phenyl] ethylidene] -N- [4- (difluoromethoxy) phenyl] -hydrazinecarboxamide or M.22B.2: N- (3-chloro-2-methylphenyl) -2 - [(4-chlorophenyl) [4- [methyl (methylsulfonyl)) amino] phenyl] methylene] -hydrazinecarboxamide;

M.23 Acetyl CoA carboxylase inhibitors, such as derivatives of tetronic and tetramatic acid, for example spirodiclofen, spiromesifene or spirotetramat;

M.24 Inhibitors of electron transport of mitochondrial complex IV, eg, M.24A phosphine such as aluminum phosphide, calcium phosphide, phosphine or zinc phosphide, or M.24B cyanide;

M.25 Mitochondrial complex II electron transport inhibitors, such as derivatives of beta-ketonitrile, eg, cenopyrafen or cyflmetofen;

M.28 Diamid class ryanodine receptor modulators, such as flubendiamide, chlorantraniliprole (rynaxypyr®), cyanthraniliprole (cyazypyr®), tetranyliprole or the phthalamide compounds M.28.1: (R) -3-Chloro-N1 - {2-methyl-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] phenyl} -N2- (1-methyl-2-methylsulfonylethyl) phthalamide 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-cyclopropylethyl) carbamoyl] phenyl} -1- (3-chlorpyridin-2-yl) -1H-pyrazole-5- carboxamide (proposed ISO name: cyclaniliprole), or the compound M.28.4: methyl-2- [3,5-dibromo-2 - ({[3-bromo-1- (3-chlorpyridin-2-yl) -1H- pyrazol-5-yl] carbonyl} amino) benzoyl] -1,2-dimethylhydrazinecarboxylate; or a compound selected from M.28.5a) to M.28.5d) and M.28.5h) to M.28.5l): M.28.5a) N- [4,6-dichloro-2 - [(diethyl-lambda-4-sulfanylidene) carbamoyl] phenyl] -2- (3-chloro-2-pyridyl) -5- (trifluoromethyl) pyrazole-3-carboxamide; M.28.5b) N- [4-chloro-2 - [(diethyl-lambda-4-sulfanylidene) carbamoyl] -6-methyl-phenyl] -2- (3-chloro-2-pyridyl) -5- (trifluoromethyl ) pyrazole-3-carboxamide; M.28.5c) N- [4-chloro-2 - [(di-2-propyl-lambda-4-sulfanylidene) carbamoyl] -6-methyl-phenyl] -2- (3-chloro-2-pyridyl) - 5- (trifluoromethyl) pyrazole-3-carboxamide; M.28.5d) N- [4,6-dichloro-2 - [(di-2-propyl-lambda-4-sulfanylidene) carbamoyl] -phenyl] -2- (3-chloro-2-pyridyl) -5- (trifluoromethyl) pyrazole-3-carboxamide; M.28.5h) N- [4,6-dibromo-2 - [(diethyl-lambda-4-sulfanylidene) carbamoyl] -phenyl] -2- (3-chloro-2-pyridyl) -5- (trifluoromethyl) pyrazole -3-carboxamide; M.28.5i) N- [2- (5-Amino-1,3,4-thiadiazol-2-yl) -4-chloro-6-methylphenyl] -3-bromo-1- (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] carbonyl] phenyl] - 1H-pyrazole-5-carboxamide; M.28.5k) 3-Bromo-N- [2,4-dichloro-6- (methylcarbamoyl) phenyl] -1- (3,5-dichloro-2-pyridyl) -1H-pyrazole-5-carboxamide; M.28.5l) N- [4-Chloro-2 - [[(1,1 dimethylethyl) amino] carbonyl] -6-methylphenyl] -1- (3-chloro-2-pyridinyl) -3- (fluoromethoxy) - 1H-pyrazole-5-carboxamide; or M.28.6: cylodiamide; or;

M.29. insecticidal active compounds of unknown or uncertain mode of action, such as afidopiropen, afoxolaner, azadiractin, amidoflumet, benzoximate, bifenazate, broflanilide, bromopropylate, cynomethionate, cryolite, dichloromezothiaz, dicofol, flufeuriflueonefomethoquin, fluopiramifluence, flupomethoquin, fluopiramifluenulfon, fluopiramulfone fluralaner, methoxadiazone, piperonyl butoxide, piflubumide, pyridylyl, pyrifluquinazon, sulfoxaflor, thioxazafen, triflumezopyrim or the compounds

M.29.3: 11- (4-chloro-2,6-dimethylphenyl) -12-hydroxy-1,4-dioxa-9-azadispiro [4.2.4.2] -tetradec-11-en-10-one, or the compound M.29.4: 3- (4'-fluoro-2,4-dimethylbiphenyl-3-yl) -4-hydroxy-8-oxa-1-azaspiro [4.5] dec-3-en-2-one, or the compound M.29.5: 1- [2-fluoro-4-methyl-5 - [(2,2,2-trifluoroethyl) sulfinyl] phenyl] -3- (trifluoromethyl) -1H-1,2,4-triazole-5- amine or active ingredients based on Bacillus firmus (Votive, I-1582); or

a compound selected from the group of M.29.6, wherein the compound is selected from M.29.6a) to M.29.6k): M.29.6a) (E / Z) -N- [1 - [(6-chloro -3-pyridyl) methyl] -2-pyridylidene] -2,2,2-trifluoro-acetamide; M.29.6b) (E / Z) -N- [1 - [(6-chloro-5-fluoro-3-pyridyl) methyl] -2-pyridylidene] -2,2,2-trifluoro-acetamide; M.29.6c) (E / Z) -2,2,2-trifluoro-N- [1 - [(6-fluoro-3-pyridyl) methyl] -2-pyridylidene] acetamide; M.29.6d) (E / Z) -N- [1 - [(6-bromo-3-pyridyl) methyl] -2-pyridylidene] -2,2,2-trifluoroacetamide; M.29.6e) (E / Z) -N- [1- [1- (6-chloro-3-pyridyl) ethyl] -2-pyridylidene] -2,2,2-trifluoroacetamide; M.29.6f) (E / Z) -N- [1 - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2-difluoro-acetamide; M.29.6g) (E / Z) -2-chloro-N- [1 - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2-difluoro-acetamide; M.29.6h) (E / Z) -N- [1 - [(2-chloropyrimidin-5-yl) methyl] -2-pyridylidene] -2,2,2-trifluoroacetamide; M.29.6i) (E / Z) -N- [1- [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2,3,3,3-pentafluoro-propanamide); M.29.6j) N- [1 - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2,2-trifluoro-thioacetamide; or M.29.6k) N- [1 - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2,2-trifluoro-N'-isopropyl-acetamidine; or the compounds

M.29.8: fluazaindolizine; or the compounds

M.29.9.a): 4- [5- (3,5-dichlorophenyl) -5- (trifluoromethyl) -4H-isoxazol-3-yl] -2-methyl-N- (1-oxothietan-3-yl) benzamide; or M.29.9.b): fluxamethamide; or

M.29.10: 5- [3- [2,6-dichloro-4- (3,3-dichloroallyloxy) phenoxy] propoxy] -1H-pyrazole; or a compound selected from the group of M.29.11, wherein the compound is selected from M.29.11b) to M.29.11p): M.29.11.b) 3- (benzoylmethylamino) -N- [2-bromo-4 - [1,2,2,3,3,3-hexafluoro-1- (trifluoromethyl) propyl] -6- (trifluoromethyl) phenyl] -2-fluoro-benzamide;

M.29.11.c) 3- (benzoylmethylamino) -2-fluoro-N- [2-iodo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- (trifluoromethyl) phenyl ]-benzamide; M.29.11.d) N- [3 - [[[2-iodo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- (trifluoromethyl) phenyl] amino] carbonyl] phenyl] -N-methyl-benzamide;

M.29.11.e) N- [3 - [[[2-bromo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- (trifluoromethyl) phenyl] amino] carbonyl] -2-fluorophenyl] -4-fluoro-N-methyl-benzamide; M.29.11.f) 4-fluoro-N- [2-fluoro-3 - [[[2-iodo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- ( trifluoromethyl) phenyl] amino] carbonyl] phenyl] -N-methyl-benzamide; M.29.11.g) 3-fluoro-N- [2-fluoro-3 - [[[2-iodo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- ( trifluoromethyl) phenyl] amino] carbonyl] phenyl] -N-methyl-benzamide;

M.29.11.h) 2-chloro-N- [3 - [[[2-iodo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- (trifluoromethyl) phenyl] amino] carbonyl] phenyl] -3-pyridinecarboxamide; M.29.11.i) 4-cyano-N- [2-cyano-5 - [[2,6-dibromo-4- [1,2,2,3,3,3-hexafluoro-1- (trifluoromethyl) - propyl] phenyl] carbamoyl] phenyl] -2-methyl-benzamide; M.29.11.j) 4-cyano-3 - [(4-cyano-2-methylbenzoyl) amino] -N- [2,6-dichloro-4- [1,2,2,3,3,3-hexafluoro -1- (trifluoromethyl) propyl] phenyl] -2-fluoro-benzamide; M.29.11.k) N- [5 - [[2-chloro-6-cyano-4- [1,2,2,3,3,3-hexafluoro-1- (trifluoromethyl) propyl] phenyl] carbamoyl] - 2-cyano-phenyl] 4-cyano-2-methyl-benzamide;

M.29.11.l) N- [5 - [[2-bromo-6-chloro-4- [2,2,2-trifluoro-1-hydroxy-1- (trifluoromethyl) ethyl] phenyl] carbamoyl] -2- cyano-phenyl] -4-cyano-2-methyl-benzamide;

M.29.11.m) N- [5 - [[2-bromo-6-chloro-4- [1,2,2,3,3,3-hexafluoro-1- (trifluoromethyl) -propyl] phenyl] carbamoyl] -2-cyano-phenyl] -4-cyano-2-methyl-benzamide; M.29.11.n) 4-cyano-N- [2-cyano-5 - [[2,6-dichloro-4- [1,2,2,3,3,3-hexafluoro-1- (trifluoromethyl) - propyl] phenyl] carbamoyl] phenyl] -2-methyl-benzamide; M.29.11.o) 4-cyano-N- [2-cyano-5 - [[2,6-dichloro-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] phenyl] carbamoyl ] phenyl] -2-methyl-benzamide;

M.29.11.p) N- [5 - [[2-bromo-6-chloro-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] phenyl] carbamoyl] -2-cyano- phenyl] -4-cyano-2-methyl-benzamide; or

a compound selected from the group of M.29.12, wherein the compound is selected from M.29.12a) to M.29.12m): M.29.12.a) 2- (1,3-Dioxan-2-yl) -6 - [2- (3-pyridinyl) -5-thiazolyl] -pyridine;

M.29.12.b) 2- [6- [2- (5-Fluoro-3-pyridinyl) -5-thiazolyl] -2-pyridinyl] -pyrimidine; M.29.12.c) 2- [6- [2- (3-pyridinyl) -5-thiazolyl] -2-pyridinyl] -pyrimidine; M.29.12.d) N-methylsulfonyl-6- [2- (3-pyridyl) thiazol-5-yl] pyridine-2-carboxamide; M.29.12.e) N-methylsulfonyl-6- [2- (3-pyridyl) thiazol-5-yl] pyridine-2-carboxamide; M.29.12.f) N-Ethyl-N- [4-methyl-2- (3-pyridyl) thiazol-5-yl] -3-methylthiopropanamide; M.29.12.g) N-Methyl-N- [4-methyl-2- (3-pyridyl) thiazol-5-yl] -3-methylthio-propanamide; M.29.12.h) N, 2-dimethyl-N- [4-methyl-2- (3-pyridyl) thiazol-5-yl] -3-methylthio-propanamide; M.29.12.i) N-Ethyl-2-methyl-N- [4-methyl-2- (3-pyridyl) thiazol-5-yl] -3-methylthio-propanamide; M.29.12.j) N- [4-chloro-2- (3-pyridyl) thiazol-5-yl] -N-ethyl-2-methyl-3-methylthio-propanamide; M.29.12.k) N- [4-chloro-2- (3-pyridyl) thiazol-5-yl] -N, 2-dimethyl-3-methylthio-propanamide; M.29.12.l) N- [4-chloro-2- (3-pyridyl) thiazol-5-yl] -N-methyl-3-methylthio-propanamide; M.29.12.m) N- [4-chloro-2- (3-pyridyl) thiazol-5-yl] -N-ethyl-3-methylthio-propanamide; or the compounds M.29.14a) 1 - [(6-Chloro-3-pyridinyl) methyl] -1,2,3,5,6,7-hexahydro-5-methoxy-7-methyl-8-nitro-imidazo [1,2-a] pyridine; or M.29.14b) 1 - [(6-chloropyridin-3-yl) methyl] -7-methyl-8-nitro-1,2,3,5,6,7-hexahydroimidazo [1,2-a] pyridine -5-ol; or the compounds

M.29.16a) 1-isopropyl-N, 5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; or M.29.16b) 1- (1,2-dimethylpropyl) -N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.16c) N, 5-dimethyl-N-pyridazin-4-yl-1- (2,2,2-trifluoro-1-methyl-ethyl) pyrazole-4-carboxamide; M.29.16d) 1- [1- (1-cyanocyclopropyl) ethyl] -N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide;

M.29.16e) N-ethyl-1- (2-fluoro-1-methyl-propyl) -5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.16f) 1- (1,2-dimethylpropyl) -N, 5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.16g) 1- [1- (1-cyanocyclopropyl) ethyl] -N, 5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.16h) N-methyl-1- (2-fluoro-1-methyl-propyl] -5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.16i) 1- (4 , 4-Difluorocyclohexyl) -N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; or M.29.16j) 1- (4,4-difluorocyclohexyl) -N, 5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide, or

M.29.17 a compound selected from compounds M.29.17a) to M.29.17j): M.29.17a) N- (1-methylethyl) -2- (3-pyridinyl) -2H-indazole-4-carboxamide; M.29.17b) N-cyclopropyl-2- (3-pyridinyl) -2H-indazole-4-carboxamide; M.29.17c) N-cyclohexyl-2- (3-pyridinyl) -2H-indazole-4-carboxamide; M.29.17d) 2 - (- pyridinyl) -N- (2,2,2-trifluoroethyl) -2H-indazole-4-carboxamide;

M.29.17e) 2- (3-pyridinyl) -N - [(tetrahydro-2-furanyl) methyl] -2H-indazole-5-carboxamide;

M.29.17f) methyl 2 - [[2- (3-pyridinyl) -2H-indazol-5-yl] carbonyl] hydrazinecarboxylate; M.29.17g) N - [(2,2-difluorocyclopropyl) methyl] -2- (3-pyridinyl) -2H-indazole-5-carboxamide; M.29.17h) N- (2,2-difluoropropyl) -2- (3-pyridinyl) -2H-indazole-5-carboxamide; M.29.17i) 2- (3-pyridinyl) -N- (2-pyrimidinylmethyl) -2H-indazole-5-carboxamide; M.29.17j) N - [(5-methyl-2-pyrazinyl) methyl] -2- (3-pyridinyl) -2H-indazole-5-carboxamide, or

M.29.18 a compound selected from compounds M.29.18a) to M.29.18d): M.29.18a) N- [3-chloro-1- (3-pyridyl) pyrazol-4-yl] -N-ethyl -3- (3,3,3-trifluoropropylsulfanyl) propanamide; M.29.18b) N- [3-chloro-1- (3-pyridyl) pyrazol-4-yl] -N-ethyl-3- (3,3,3-trifluoropropylsulfinyl) propanamide;

M.29.18c) N- [3-chloro-1- (3-pyridyl) pyrazol-4-yl] -3 - [(2,2-difluorocyclopropyl) methylsulfanyl] -N-ethyl-propanamide; M.29.18d) N- [3-chloro-1- (3-pyridyl) pyrazol-4-yl] -3 - [(2,2-difluorocyclopropyl) methylsulfinyl] -N-ethyl-propanamide; or the compound M.29.19 sarolaner, or the compound

The commercially available compounds of group M listed above can be found in "The Pesticide Manual, 16th Edition, C. MacBean, British Crop Protection Council (2013)" among other publications. Pesticide Manual Online is updated regularly and can be accessed via http://bcpcdata.com/pesticidemanual.html. Another online database for pesticides that provides ISO common names is http://www.alanwood.net/pesticides. The neonicotinoid cycloxaprid M.4 is known from WO2010 / 069266 and WO2011 / 069456, the neonicotinoid M.4A.2, sometimes also called guadipir, is known from WO2013 / 003977, and the neonicotinoid M.4A.3 (approved as paichongding in China) is known from WO2007 / 101369. The M.22B.1 metaflumizone analog is described in CN10171577 and the M.22B.2 analog is described in CN102126994. Phthalamides M.28.1 and M.28.2 are known from WO2007 / 101540. Anthranilamide M.28.3 is described in WO2005 / 077934. The hydrazide compound M.28.4 is described in WO2007 / 043677. Anthranilamides M.28.5a) to M.28.5d) and M.28.5h) are described in WO 2007/006670, WO2013 / 024009 and WO2013 / 024010, anthranilamide M.28.5i) is described in WO2011 / 085575, M .28.5j) in WO2008 / 134969, M.28.5k) in US2011 / 046186 and M.28.5l) in WO2012 / 034403. The diamide compound M.28.6 can be found in WO2012 / 034472. The spirochetal substituted cyclic ketoenol derivative M.29.3 is known from WO2006 / 089633 and the biphenyl substituted spirocyclic ketoenol derivative M.29.4 from WO2008 / 067911. Triazoylphenylsulfide M.29.5 is described in WO2006 / 043635, and biological control agents based on Bacillus firmus are described in WO2009 / 124707. Compounds M.29.6a) to M.29.6i) listed in M.29.6 are described in WO2012 / 029672, and M.29.6j) and M.29.6k) in WO2013 / 129688. Nematicide M.29.8 is known from WO2013 / 055584. Isoxazoline M.29.9.a) is described in WO2013 / 050317. Isoxazoline M.29.9.b) is described in WO2014 / 126208. The pyridyl-type analog M.29.10 is known from WO2010 / 060379. The carboxamides broflanilide and M.29.11.b) to M.29.11.h) are described in WO2010 / 018714, and the carboxamides M.29.11i) to M.29.11.p) in WO2010 / 127926. Pyridylthiazoles M.29.12.a) to M.29.12.c) are known from WO2010 / 006713, M.29.12.d) and M.29.12.e) are known from WO2012 / 000896 and M.29.12.f) M. 29.12.m) of WO2010 / 129497. Compounds M.29.14a) and M.29.14b) are known from WO2007 / 101369. The pyrazoles M.29.16.a) to M.29.16h) are described in documents WO2010 / 034737, WO2012 / 084670 and WO2012 / 143317, respectively, and the pyrazoles M.29.16i) and M.29.16j) are described in US 61/891437. Pyridinylindazoles M.29.17a) to M.29.17.j) are described in WO2015 / 038503. Pyridylpyrazoles M.29.18a) to M.29.18d) are described in US2014 / 0213448. Isoxazoline M.29.19 is described in WO2014 / 036056. Isoxazoline M.29.20 is known from WO2014 / 090918.

The following list of fungicides, in conjunction with which pesticide mixtures can be used, is intended to illustrate, but does not limit, the possible combinations:

A) Respiratory inhibitors

- Complex III inhibitors at the Qo site (for example, strobilurins): azoxystrobin (A.1.1), coumethoxystrobin (A.1.2), coumoxystrobin (A.1.3), dimoxystrobin (A.1.4), enestroburin (A.1.5) , fenaminstrobin (A.1.6), phenoxystrobin / flufenoxystrobin (A.1.7), fluoxastrobin (A.1.8), kresoxim-methyl (A.1.9), mandestrobin (A.1.10), metominostrobin (A.1.11), orisastrobin (A .1.12), picoxystrobin (A.1.13), pyractrostrobin (A.1.14), pymetostrobin (A. 1.15), pyraoxystrobin ( ^a . 1.16), trifloxystrobin (A.1.17), 2- (2- (3- (2, 6-dichlorophenyl) -1-methyl-allylideneaminoxymethyl) -phenyl) -2-methoxyimino-N-methyl-acetamide (A.1.18), pyribencarb (A.1.19), triclopyricarb / chlorodincarb (A.1.20), famoxadone (A. 1.21), fenamidone (A.1.21), methyl-N- [2 - [(1,4-dimethyl-5-phenyl-pyrazol-3-yl) oxylmethyl] phenyl] -N-methoxy-carbamate (A.1.22) , 1- [3-chloro-2 - [[1- (4-chlorophenyl) -1H-pyrazol-3-yl] oxymethyl] phenyl] -4-methyl-tetrazol-5-one (A.1.23), 1- [3-bromo-2 - [[1- (4-chlorophenyl) pyrazol-3-yl] oxymethyl] phenyl] -4-methyl-tetraz ol-5-one (A.1.24), 1- [2 - [[1- (4-chlorophenyl) pyrazol-3-yl] oxymethyl] -3-methylphenyl] -4-methyl-tetrazol-5-one (A .1.25), 1- [2 - [[1- (4-chlorophenyl) pyrazol-3-yl] oxymethyl] -3-fluoro-phenyl] -4-methyl-tetrazol-5-one (A.1.26), 1 - [2 - [[1- (2,4-dichlorophenyl) pyrazol-3-yl] oxymethyl] -3-fluoro-phenyl] -4-methyl-tetrazol-5-one (A.1.27), 1- [2 - [[4- (4-chlorophenyl) thiazol-2-yl] oxymethyl] -3-methyl-phenyl] -4-methyl-tetrazol-5-one (A.1.28), 1- [3-chloro-2- [[4- (p-tolyl) thiazol-2-yl] oxymethyl] phenyl] -4-methyl-tetrazol-5-one (A.1.29), 1- [3-cyclopropyl-2 - [[2-methyl- 4- (1-methylpyrazol-3-yl) phenoxy] methyl] phenyl] -4-methyl-tetrazol-5-one (A.1.30), 1- [3- (difluoromethoxy) -2 - [[2-methyl- 4- (1-methylpyrazol-3-yl) phenoxy] methyl] phenyl] -4-methyl-tetrazol-5- one (A.1.31), 1-methyl-4- [3-methyl-2 - [[2- methyl-4- (1-methylpyrazol-3-yl) phenoxy] methyl] phenyl] tetrazol-5-one (A.1.32), 1-methyl-4- [3-methyl-2 - [[1 - [3 - (trifluoromethyl) phenyl] -ethylideneamino] oxymethyl] phenyl] tetrazol-5-one (A.1.33), (Z, 2E) -5- [1- (2,4-dichlorophenyl) pyrazol-3-yl] -oxy -2-methoxyimino-N, 3-dimethyl-pent-3-enamid a (A.1.34), (Z, 2E) -5- [1- (4-chlorophenyl) pyrazol-3-yl] oxy-2-methoxyimino- N, 3-dimethyl-pent-3-enamide (A.1.35 ), (Z, 2E) -5- [1- (4-chloro-2-fluoro-phenyl) pyrazol-3-yl] oxy-2-methoxyimino-N, 3-dimethyl-pent-3-enamide (A. 1.36), complex III inhibitors at the Qi site: ciazofamide (A.2.1), amisulbrom (A.2.2), [(3S, 6S, 7R, 8R) -8-benzyl-3 - [(3 -acetoxy-4-methoxy-pyridine-2-carbonyl) amino] -6-methyl-4,9-dioxo-1,5-dioxonan-7-yl] (A.2.3), [(3S, 6S, 7R, 8R) -8-benzyl-3 - [[3- (acetoxymethoxy) -4-methoxy-pyridine-2-carbonyl] amino] -6-methyl-4,9-dioxo-1,5-dioxonan- 7-yl] (A.2.4), [(3S, 6S, 7R, 8R) -8-benzyl-3 - [(3-isobutoxycarbonyloxy-4-methoxy-pyridine-2-carbonyl) amino] - 6-methyl-4,9-dioxo-1,5-dioxonan-7-yl] (A.2.5), [(3S, 6S, 7R, 8R) -8-benzyl-3 - [[3 - (1,3-benzodioxol-5-ylmethoxy) -4-methoxy-pyridine-2-carbonyl] amino] -6-methyl-4,9-dioxo-1,5-dioxonan-7-yl] (A.2.6 ); (3S, 6S, 7R, 8R) -3 - [[(3-hydroxy-4-methoxy-2-pyridinyl) carbonyl] amino] -6-methyl-4,9-dioxo-8- (phenylmethyl ) -1,5-dioxonan-7-yl (A.2.7), (3S, 6S, 7R, 8R) -8-benzyl-3- [3 - [(isobutyryloxy) methoxy] -4-methoxypicolinamide isobutyrate] - 6-methyl-4,9-dioxo-1,5-dioxonan-7-yl (A.2.8);

- complex II inhibitors (e.g. carboxamides): benodanyl (A.3.1), benzovindiflupir (A.3.2), bixafen (A.3.3), boscalid (A.3.4), carboxin (A.3.5), fenfuram (A .3.6), fluopyram (A.3.7), flutolanil (A.3.8), fluxapyroxad (A.3.9), furametpyr (A.3.10), isofetamid (A.3.11), isopyrazam (A.3.12), mepronil (A. 3.13), oxycarboxin (A.3.14), penflufen (A.3.14), penthiopyrad (A.3.15), sedaxane (A.3.16), tecloftalam (A.3.17), thifluzamide (A.3.18), N- (4 ' -trifluoromethylthiobiphenyl-2-yl) -3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxamide (A.3.19), N- (2- (1,3,3-trimethyl-butyl) -phenyl) -1 , 3-dimethyl-5-fluoro-1H-pyrazole-4-carboxamide (A.3.20), 3- (difluoromethyl) -1-methyl-N- (1,1,3-trimethylindan-4-yl) pyrazole-4 -carboxamide (A.3.21), 3- (trifluoromethyl) -1-methyl-N- (1,1,3-trimethylindan-4-yl) pyrazole-4-carboxamide (A.3.22), 1,3-dimethyl- N- (1,1,3-trimethylindan-4-yl) pyrazole-4-carboxamide (A.3.23), 3- (trifluoromethyl) -1,5-dimethyl-N- (1,1,3-trimethylindan-4 -yl) pyrazole-4-carboxamide (A.3.24), 1,3,5-trimethyl-N- (1,1,3-tri methylindan-4-yl) pyrazole-4-carboxamide (A.3.25), N- (7-fluoro-1,1,3-trimethyl-indan-4-yl) -1,3-dimethylpyrazole-4-carboxamide (A .3.26), N- [2- (2,4-dichlorophenyl) -2-methoxy-1-methyl-ethyl] -3- (difluoromethyl) -1-methyl-pyrazole-4-carboxamide (A.3.27);

- other respiration inhibitors (eg complex I, uncouplers): diflumetorim (A.4.1), (5,8-difluoroquinazolin-4-yl) - {2- [2-fluoro-4- (4-trifluoromethylpyridine- 2-yloxy) -phenyl] -ethyl} -amine (A.4.2); nitrophenyl derivatives: binapacryl (A.4.3), dinobuton (A.4.4), dinocap (A.4.5), fluazinam (A.4.6); ferimzone (A.4.7); Organometallic compounds: salts of fenthin, such as fenthin acetate (A.4.8), fenthin chloride (A.4.9) or phenthin hydroxide (A.4.10); Amethoctradine (A.4.11); and silthofam (A.4.12);

B) Sterol biosynthesis inhibitors (SBI fungicides)

- o Demethylase C14 inhibitors (DMI fungicides): triazoles: azaconazole (B.1.1), bitertanol (B.1.2), bromuconazole (B.1.3), cyproconazole (B.1.4), difenoconazole (B.1.5), diniconazole (B.1.6), diniconazole-M (B.1.7), epoxiconazole (B.1.8), fenbuconazole (B.1.9), fluquinconazole (B.1.10), flusilazole (B.1.11), flutriafol (B.1.12), hexaconazole (B.1.13), imibenconazole (B.1.14), ipconazole (B.1.15), metconazole (B.1.17), myclobutanil (b .1.18), oxpoconazole (B.1.19), paclobutrazol (B.1.20), penconazole (B.1.21), propiconazole (B.1.22), ^{prothioconazole (b} .1.23), simeconazole (B.1.24), tebuconazole (B.1.25), tetraconazole (B.1.26), triadimefon (B.1.27), triadimenol ( B.1.28), triticonazole (B.1.29), uniconazole (B.1.30), 1- [rel- (2S; 3R) -3- (2-chlorophenyl) -2- (2,4-difluorophenyl) -oxyranylmethyl] -5- thiocyanate-1H- [1,2,4] triazole (B.1.31), 2- [rel- (2S, 3R) -3- (2-chlorophenyl) -2- (2,4-difluorophenyl) - oxiranylmethyl] -2H- [1,2,4] triazole-3-thiol (B.1.32), 2- [2-chloro-4- (4-chlorophenoxy) phenyl] -1- (1,2,4-triazole -1-yl) pentan-2-ol (B. 1.33), 1- [4- (4-chlorophenoxy) -2- (trifluoromethyl) phenyl] -1-cyclopropyl-2- (1,2,4-triazol-1-yl) ethanol (B.1.34), 2- [4- (4-chlorophenoxy) -2- (trifluoromethyl) phenyl] -1- (1,2,4-triazol-1-yl) butan-2-ol (B.1.35), 2- [2-chloro- 4- (4-chlorophenoxy) phenyl] -1- (1,2,4-triazol-1-yl) butan-2-ol (B.1.36), 2- [4- (4-chloro-phenoxy) -2 - (trifluoromethyl) phenyl] -3-methyl-1- (1,2,4-triazol-1-yl) butan-2-ol (B.1.37), 2- [4- (4-chlorophenoxy) -2- (trifluoromethyl) phenyl] -1- (1,2,4-triazol-1-yl) propan-2-ol (B.1.38), 2- [2-chloro-4- (4-chlorophenoxy) phenyl] -3 -methyl-1- (1,2,4-triazol-1-yl) butan-2-ol (B.1.39), 2- [4- (4-chlorophenoxy) -2- (trifluoromethyl) phenyl] -1- (1,2,4-triazol-1-yl) pentan-2-ol (B.1.40), 2- [4- (4-fluorophenoxy) -2- (trifluoromethyl) phenyl] -1- (1,2, 4-triazol-1-yl) propan-2-ol (B.1.41), 2- [2-chloro-4- (4-chlorophenoxy) phenyl] -1- (1,2,4-triazol-1-yl ) pent-3-in-2-ol (B.1.51); imidazoles: imazalil (B.1.42), pefurazoate (B.1.43), prochloraz (B.1.44), triflumizole (B.1.45); pyrimidines, pyridines and piperazines: fenarimol (B.1.46), nuarimol (B.1.47), pyrifenox (B.1.48), triporin (b .1.49), [3- (4-chloro-2-fluoro-phenyl) -5 - (2,4-Difluorophenyl) isoxazol-4-yl] - (3-pyridyl) methanol (B.1.50);

- Delta14-reductase inhibitors: aldimorph (B.2.1), dodemorf (B.2.2), dodemorph acetate (B.2.3), fenpropimorph (B.2.4), tridemorph (B.2.5), fenpropidine (B.2.6 ), piperaline (B.2.7), spiroxamine (B.2.8);

- 3-keto reductase inhibitors: fenhexamide (B.3.1);

C) nucleic acid synthesis inhibitors

- Phenylamides or acylamino acid fungicides: benalaxyl (C.1.1), benalaxyl-M (C.1.2), kiralaxil (C.1.3), metalaxyl (C.1.4), metalaxyl-M (mefenoxam, C.1.5), ofurace ( C.1.6), oxadixyl (C.1.7);

- others: hymexazole (C.2.1), octilinone (C.2.2), oxolinic acid (C.2.3), bupyrimate (C.2.4), 5-fluorocytosine (C.2.5), 5-fluoro-2- (p- tolylmethoxy) pyrimidin-4-amine (C.2.6), 5-fluoro-2- (4-fluorophenylmethoxy) pyrimidin-4-amine (C.2.7);

D) Inhibitors of cell division and cytoskeleton.

- tubulin inhibitors, such as benzimidazoles, thiophanates: benomyl (D1.1), carbendazim (D1.2), fuberidazole (D1.3), thiabendazole (D1.4), thiophanate-methyl (D1.5); triazolopyrimidines: 5-chloro-7- (4-methylpiperidin-1-yl) -6- (2,4,6-trifluorophenyl) - [1,2,4] triazolo [1,5-a] pyrimidine (D1.6 );

- other inhibitors of cell division: dietofencarb (D2.1), ethaboxam (D2.2), pencycuron (D2.3), fluopicolide (D2.4), zoxamide (D2.5), metrafenone (D2.6), pyrophenone (D2.7);

E) Inhibitors of amino acid and protein synthesis.

- methionine synthesis inhibitors (anilino-pyrimidines): cyprodinil (E.1.1), mepanipyrim (E.1.2), pyrimethanil (E.1.3);

- protein synthesis inhibitors: blasticidin-S (E.2.1), kasugamycin (E.2.2), kasugamycin hydrochloride (E.2.3), mildiomycin (E.2.4), streptomycin (E.2.5), oxytetracycline (E .2.6), polyoxin (E.2.7), validamycin A (E.2.8);

F) signal transduction inhibitors

- MAP / histidine kinase inhibitors: fluoroimide (F.1.1), iprodione (F.1.2), procymidone (F.1.3), vinclozolin (F.1.4), fenpiclonil (F.1.5), fludioxonil (F.1.6);

- G protein inhibitors: quinoxyphene (F.2.1);

G) lipid and membrane synthesis inhibitors

- Inhibitors of phospholipid biosynthesis: edifenfos (G.1.1), iprobenfos (G.1.2), pyrazofos (G.1.3), isoprothiolane (G.1.4);

- lipid peroxidation: dichloran (G.2.1), quintacene (G.2.2), technacene (G.2.3), tolclofos-methyl (G.2.4), biphenyl (G.2.5), chloroneb (G.2.6), etridiazole ( G.2.7);

- phospholipid biosynthesis and cell wall deposition: dimethomorf (G.3.1), flumorf (G.3.2), mandipropamide (G.3.3), pirimorf (G.3.4), bentiavalicarb (G.3.5), iprovalicarb (G. 3.6), valifenalate (G.3.7) and N- (1- (1- (4-cyano-phenyl) ethanesulfonyl) -but-2-yl) carbamic acid (4-fluorophenyl) ester (G.3.8);

- compounds that affect the permeability of the cell membrane and fatty acids: propamocarb (G.4.1);

- fatty acid amide hydrolase inhibitors: oxathiapiproline (G.5.1), 2- {3- [2- (1 - {[3,5-bis (difluoromethyl-1H-pyrazol-1-yl) acetyl} piperidin- 4-yl) -1,3-thiazol-4-yl] -4,5-dihydro-1,2-oxazol-5-yl} phenyl methanesulfonate (G.5.2), 2- {3- [2- (1 - {[3,5-bis (difluoromethyl) -1H-pyrazol-1-yl] acetyl} piperidin-4-yl) 1,3-thiazol-4-yl] -4,5-dihydro-1,2-oxazole -5-yl} -3-chlorophenyl methanesulfonate (G.5.3);

H) Inhibitors with multisite action

- inorganic active substances: Bordeaux mixture (H.1.1), copper acetate (H.1.2), copper hydroxide (H.1.3), copper oxychloride (H.1.4), basic copper sulfate (H.1.5) , sulfur (H.1.6);

- thio and dithiocarbamates: ferbam (H.2.1), mancozeb (H.2.2), maneb (H.2.3), metam (H.2.4), metiram (H.2.5), propineb (H.2.6), thiram (H .2.7), zineb (H.2.8), ziram (H.2.9);

- organochlorine compounds (e.g. phthalimides, sulfa drugs, chloronitriles): anilazine (H.3.1), chlorothalonil (H.3.2), captafol (H.3.3), captan (H.3.4), folpet (H.3.5), dichlorofluanide (H.3.6), dichlorophene (H.3.7), hexachlorobenzene ( ^h .3.8), pentachlorophenol (H.3.9) and its salts, phthalide (H.3.10), tolylfluanide (H.3.11), N- (4-chloro -2-nitro-phenyl) -N-ethyl-4-methylbenzenesulfonamide (H.3.12);

- guanidines and others: guanidine (H.4.1), dodyne (H.4.2), dodyne free base (H.4.3), guazatine (H.4.4), guazatine acetate (H.4.5), iminoctadine (H.4.6 ), iminoctadin-triacetate (H.4.7), iminoctadin-tris (albesilate) (H.4.8), dithianon (H.4.9), 2,6-dimethyl-1H, 5H- [1,4] dithiino [2,3 -c: 5,6-c '] dipyrrole-1,3,5,7 (2H, 6H) -tetraone (H.4.10);

I) inhibitors of cell wall synthesis

- glucan synthesis inhibitors: validamycin (I.1.1), polyoxin B (I.1.2);

- melanin synthesis inhibitors: pyroquilon (I.2.1), tricyclazole (I.2.2), carpropamid (1.2.3), dicyclomet (I.2.4), phenoxanil (1.2.5);

J) Plant defense inducers

- acibenzolar-S-methyl (J.1.1), probenazole (J.1.2), isothianil (J.1.3), thiadinyl (J.1.4), prohexadione-calcium (J.1.5); phosphonates: fosetyl (J.1.6), fosetyl-aluminum (J.1.7), phosphorous acid and its salts (J.1.8), potassium or sodium bicarbonate (J.19);

K) Unknown mode of action

- bronopol (K.1.1), quinomethionate (K.1.2), cyflufenamide (K.1.3), cymoxanil (K.1.4), dazomet (K.1.5), debacarb (K.1.6), diclomezine ( ^k .1.7), difenzoquat (K.1.8), difenzoquat-methylsulfate (K.1.9), diphenylamine (K.1.10), phenpyrazamine (K.1.11), flumetover (K.1.12), flusulfamide (K.1.13), flutianil (K.1.14) , metasulfocarb (k .1.15), nitrapyrin (K.1.16), nitrotal-isopropyl (K.1.18), oxathiapiproline (K.1.19), tolprocarb (K.1.20), oxyn-copper (k .1.21), proquinazid (K .1.22), tebufloquin (K.1.23), tecloftalam (K.1.24), triazoxide (K.1.25), 2-butoxy-6-iodo-3-propylchromen-4-one (K.1.26), 2- [3 , 5-bis (difluoromethyl) -1H-pyrazol-1-yl] -1- [4- (4- {5- [2- (prop-2-y-1-yloxy) phenyl] -4,5-dihydro -1,2-oxazol-3-yl} -1,3-thiazol-2-yl) piperidin-1-yl] ethanone (K.1.27), 2- [3,5-bis (difluoromethyl) -1H-pyrazole -1-yl] -1- [4- (4- {5- [2-fluoro-6- (prop-2-yn-1-yl-oxy) phenyl] -4,5-dihydro-1,2- oxazol-3-yl} -1,3-thiazol-2-yl) piperidin-1-yl] ethanone (K.1.28), 2- [3,5-bis (difluoromethyl) -1H-pyrazol-1-yl] -1 - [4- (4- {5- [2-chloro-6- (prop-2-in -1-yloxy) phenyl] -4,5-dihydro-1,2-oxazol-3-yl} -1,3-thiazol-2-yl) piperidin-1-yl] ethanone (K.1.29), N- (cyclopropylmethoxyimino- (6-difluoro-methoxy-2,3-difluoro-phenyl) -methyl) -2-phenyl acetamide (K.1.30), N '- (4- (4-chloro-3-trifluoromethyl-phenoxy) - 2,5-dimethyl-phenyl) -N-ethyl-N-methylformamidine (K.1.31), N '- (4- (4-fluoro-3-trifluoromethylphenoxy) -2,5-dimethyl-phenyl) -N-ethyl -N-methyl formamidine (K.1.32), N '- (2-methyl-5-trifluoromethyl-4- (3-trimethylsilanyl-propoxy) -phenyl) -N-ethyl-N-methylformamidine (K.1.33), N '- (5-Difluoromethyl-2-methyl-4- (3-tri-methylsilanyl-propoxy) -phenyl) -N-ethyl-N-methylformamidine (K.1.34), 6-tert-butyl-8-fluoro-2 , 3-dimethyl-quinolin-4-yl ester of methoxyacetic acid (K.1.35), 3- [5- (4-methylphenyl) -2,3-dimethyl-isoxazolidine-3-yl] -pyridine (K.1.36) , 3- [5- (4-chloro-phenyl) -2,3-dimethyl-isoxazolidin-3-yl] pyridine (pyrisoxazole) (K.1.37), (6-methoxy-pyridin-3-yl acid N-amide ) cyclopropanecarboxylic (K.1.38), 5-chloro-1- (4,6-dimethoxy-pyrimidin-2-yl) -2-methyl -1H-benzoimidazole (K.1.39), 2- (4-chloro-phenyl) -N- [4- (3,4-dimethoxy-phenyl) -isoxazol-5-yl] -2-prop-2-ynyloxy-acetamide, ethyl (Z) -3-amino-2-cyano-3-phenyl- prop-2-enoate (K.1.40), picarbutrazox (K.1.41), pentyl N- [6 - [[(Z) - [(1-methyltetrazol-5-yl) -phenyl-methylene] amino] oxymethyl] - 2-pyridyl] carbamate (K.1.42), 2- [2 - [(7,8-difluoro-2-methyl-3-quinolyl) oxy] -6-fluoro-phenyl] propan-2-ol (K.1.43 ), 2- [2-fluoro-6 - [(8-fluoro-2-methyl-3-quinolyl) oxy] phenyl] propan-2-ol (K.1.44), 3- (5-fluoro-3,3 , 4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl) quinoline (K.1.45), 3- (4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl) quinoline (K.1.46), 3- (4,4,5-trifluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl) quinoline (K.1.47), 9-fluoro-2,2-dimethyl- 5- (3-quinolyl) -3H-1,4-benzoxazepine (K.1.48).

The fungicides described by common names, their preparation and their activity, for example, against harmful fungi are known (cf .: http://www.alanwood.net/pesticides/); these substances are commercially available. The fungicides 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 141 317; EP-A 152031; EP -A 226917; EP-A 243970; EP-A 256503; EP-A 428941; EP-A 532022; EP-A 1028 125; EP-A 1035122; EP-A 1201 648; EP-A 1122244, 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 03/11853; 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 11/028657, WO 2012/168188, WO 2007/006670, WO 2011/77514; WO 13/047749, WO 10/069882, WO 13/047441, WO 03/16303, WO 09/90181, WO 13/007767, WO 13/010862, WO 13/127704, WO 13/024009, WO 1 3/024010 and WO 13/047441, WO 13/162072, WO 13/092224, WO 11/135833).

Suitable additional compounds C also include biopesticides. Biopesticides have been defined as a form of pesticides based on microorganisms (bacteria, fungi, viruses, nematodes, etc.) or natural products (compounds, such as metabolites, proteins or extracts from biological sources or other natural sources) (Protection Agency United States Environmental: http://www.epa.gov/pesticides/biopesticides/). Biopesticides are divided into two main classes, microbial and biochemical pesticides:

(1) Microbial pesticides consist of bacteria, fungi, or viruses (and often include the metabolites that bacteria and fungi produce). Entomopathogenic nematodes are also classified as microbial pesticides, even though they are multicellular.

(2) Biochemical pesticides are natural substances or structurally similar and functionally identical to a natural substance and extracts from biological sources that control pests or provide other crop protection uses as defined below, but have a non-toxic mode of action (such as growth or developmental regulation, attractants, repellants, or defense activators (eg, induced resistance) and are relatively non-toxic to mammals.

Biopesticides for use against crop diseases have already become established in a variety of crops. For example, biopesticides already play an important role in the control of mildew diseases. Its benefits include: a 0 day pre-harvest interval, the ability to use under moderate to severe disease pressure, and the ability to use in a mix or on a rotation schedule with other registered pesticides. An important growth area for biopesticides is in the area of seed treatments and soil amendments. Biopesticidal seed treatments are, for example, used to control soil-borne fungal pathogens that cause seed rot, damping, root rot and seedling blight. They can also be used to control internal seed-borne fungal pathogens as well as fungal pathogens found on the seed surface. Many biopesticide products also show capabilities to stimulate plant host defenses and other physiological processes that can make treated crops more resistant to a variety of biotic and abiotic stresses or can regulate plant growth. Many biopesticide products also show abilities to stimulate plant health, plant growth, and / or performance enhancing activity.

The following list of biopesticides, in conjunction with which the pesticidal mixtures of the present invention can be used, is intended to illustrate, but not limit, possible combinations:

L) Biopesticides

L1) Microbial pesticides with fungicidal, bactericidal, viricidal and / or plant defense activator activity: Ampelomyces quisqualis, Aspergillus flavus, Aureobasidium pullulans, Bacillus altitudinis, B. megaterium, B. mojavensis, B. mycoides, B. pumilus, B. simplex , B. solisalsi, B. subtilis, 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 alvei, PaeniBacillus polymyxa, Pantoea vagans, Penicillium bilaiae, Phlebiopsis gigantea, Pseudomonas sp., Pseudomonas chloraphis, Pseudozyma flocculosa, Pichia anomalaiseocyromania violaceis, Stiddenomycidium, Pichia anomalaiseoptium, Pythium griocidium, Pichia anomalaviruses , Talaromyces flavus, Trichoderma asperelloides, T. asperellum, T. atroviride, T. fertile, T. gamsii, T. harmatum, T. harzianum, T. polysporum, T. stromaticum, T. virens, T. viride, Typhula phacorrhiza, Ulocladium oudemansii, Verticillium dahlia, zucchini yellow mosaic virus (avirulent strain);

L2) Biochemical pesticides with activating activity of fungal, bactericidal, viricidal and / or vegetal defense: hairpin protein, Reynoutria sachalinensis extract;

L3) Microbial pesticides with insecticidal, acaricidal, molluscid and / or nematicidal activity: Agrobacterium radiobacter, Bacillus cereus, B. firmus, B. thuringiensis, B. thuringiensis ssp. aizawai, B. t. ssp. israelensis, B. t. ssp. galleriae, B. t. ssp. kurstaki, B. t. ssp. tenebrionis, Beauveria bassiana, B. brongniartii, Burkholderia spp., Chromobacterium subtsugae, Cydia pomonella granulovirus ( CpGV), Cryptophlebia leucotreta granulovirus (CrleGV), Flavobacterium spp., Helicoverpa nucleopolyhedrovirus of Helicoverpa Helicoverphedrovirus Helicoverphedrovirus single capsid nucleus of Helicoverpavirus nucleo-capsid (HzNPV), Helicoverpa zea single capsid nucleopolyhedrovirus (HzSNPV), Heterorhabditis bacteriophora, Isaria fumosorosea, Lecanicillium longisporum, L. muscarium, Metarhizium anisopliae, Metarhizium anisopliae var. anisopliae, M. anisopliae var. acridum, Nomuraea rileyi, Paecilomyces fumosoroseus, P. lilacinus, PaeniBacillus popilliae, Pasteuria spp., P. nishizawae, P. penetrans, P. ramosa, P. thornea, P. usgae, Pseudomonas fluorescens, nucleopolyhedrovirus of Spodoptera littoralis ) Steinernema carpocapsae, S. feltiae, S. kraussei, Streptomyces galbus, S. microflavus;

L4) Biochemical pesticides with insecticidal, acaricidal, molluscid, pheromone and / or nematicidal activity: L-carvone, citral, (E, Z) -7,9-dodecadiene-1-yl acetate, ethyl formate, (E, Z) Ethyl -2,4-decadienoate (pear ester), (Z, Z, E) -7,11,13-hexadecatrienal, heptyl butyrate, isopropyl myristate, lavenderyl Senecioate, 2-methyl 1-butanol, methyl eugenol, methyl jasmonate, (E, Z) -2,13-octadecadien-1-ol, (E, Z) -2,13-octadecadiene-1-ol acetate, (E, Z) -3,13-octadecadien- 1-ol, R-1-octen-3-ol, pentatermanone, (E, Z, Z) -3,8,11-tetradecatrienyl acetate, (Z, E) -9,12-tetradecadien-1-yl acetate , Z-7-tetradecen-2-one, Z-9-tetradecen-1-yl acetate, Z-11-tetradecenal, Z-11-tetradecen-1-ol, Chenopodium ambrosiodes extract, Neem oil, Quillai;

L5) Microbial pesticides with plant stress reduction, plant growth regulator, plant growth promoting activity and / or performance improvement: Azospirillum amazonense, A. brasilense, A. lipoferum, A. irakense, A. halopraeferens, Bradyrhizobium spp., B. elkanii, B. japonicum, B. liaoningense, B. lupini, Delftia acidovorans, Glomus intraradices, Mesorhizobium spp., Rhizobium leguminosarum bv. phaseoli, RI bv. trifolii, RI bv. viciae, R. tropici, Sinorhizobium meliloti.

The biopesticides of group L1) and / or L2) may also have insecticidal, acaricidal, molluscid, pheromone, nematicidal, plant stress reducer, plant growth regulator, plant growth promoting and / or yield enhancing activity. Biopesticides of group L3) and / or L4) may also have fungicidal, bactericidal, viricidal, plant defense activator, plant stress reducer, plant growth regulator, plant growth promoting activity and / or performance enhancer. The biopesticides of group L5) can also have fungicidal, bactericidal, viricidal, plant defense activator, insecticidal, acaricidal, molluscid, pheromone and / or nematicidal activity.

Many of these biopesticides have been deposited under the deposit numbers mentioned in this document (the premises such as ATCC or DSM refer to the acronym of the respective culture collection, for more details see, for example, here: http: // www. Wfcc.info/ccinfo/collection/by_acronym/), mentioned in the literature, registered and / or commercially available: mixtures of Aureobasidium pullulans DSM14940 and DSM14941 isolated in 1989 in Konstanz, Germany (e.g. blastospores in BlossomProtect ® from bio-ferm GmbH, Austria), Azospirillum brasilense Sp245 originally isolated in the wheat region of southern Brazil (Passo Fundo) at least before 1980 (BR 11005; for example, GELFIX® Grasses from BASF Agricultural Specialties Ltd., Brazil), strains of A. brasilense Ab-V5 and Ab-V6 (for example, in AzoMax from Novozymes BioAg Produtos papra Agricultura Ltda., Quattro Barras, Brazil or Simbiose-Maíz® from Simbiose-Agro, Brazil; Plant Soil 331, 413-425, 2010), B. firmu s CNCM I-1582, a variant of the parental strain EIP-N1 (CNCM I-1556) isolated from the soil of the plain central area of Israel (WO2009 / 126473, US 6,406,690; for example, Votivo® from Bayer CropScience LP, United States), B. pumilus GHA 180 isolated from the apple rhizosphere in Mexico (IDAC 260707-01; for example, PRO-MIX® bX from Premier Horticultura, Quebec, Canada), B. pumilus INR-7 otherwise referred to as BU-F22 and BU-F33 isolated at least before 1993 from cucumber infested by Erwinia tracheiphila (NRRL 0-50185, n Rr L 0-50153; US 8,445,255), B. pumilus KFP9F isolated from the rhizosphere of grasses in South Africa in less than before 2008 (NRRL O-50754; WO2014 / 029697; for example, BAC-UP or FUSION-P from BASF Agricultural Specialties (Pty) Ltd., South Africa), B. pumilus QST 2808 was isolated from soil collected in Pohnpei, Federated States of Micronesia, in 1998 (NRRL O-30087; for example, Sonata® or Ballad® Plus from Bayer Crop Science LP, USA), B. simplex ABU 288 (NRRL O -50304; US 8,445,255), B. subtilis FB17 also called UD 1022 or UD10-22 isolated from red beet roots in North America (ATCC PTN-11857; System. Appl. Microbiol. 27, 372 -379, 2004; US 2010/0260735; WO 2011/109395); B. thuringiensis ssp. aizawai ABTS-1857 isolated from soil taken from a lawn in Ephraim, Wisconsin, United States, in 1987 (also called ABG-6346; ATCC SD-1372; for example, XenTari® from BioFa AG, Münsingen, Germany), B. t . ssp. kurstaki ABTS-351 identical to HD-1 isolated in 1967 from diseased black larvae from Pink Bollworm in Brownsville, Texas, USA (ATCC SD-1275; eg Dipel® DF from Valent BioSciences, IL, USA), B. t. ssp. kurstaki SB4 isolated from larval carcasses of E. saccharina (NRRL O-50753; for example, Beta Pro® from BASF Agricultural Specialties (Pty) Ltd., South Africa), B. t. ssp. tenebrionis NO-176-1, a mutant of strain NB-125, a wild-type strain isolated in 1982 from a dead pupa of the Tenebrio molitor beetle (DSM 5480; EP 585 215 B1; for example, Novodor® from Valent BioSciences, Switzerland), Beauveria bassiana GHA (A ^t CC 74250; for example, BotaniGard® 22WGP from Laverlam Int. Corp., USA), B. bassiana JW-1 (ATCC 74040; for example, Naturalis® from CBC (Europe) Srl , Italy), B. bassiana PPRI 5339 isolated from the larva of the tortoise beetle Conchyloctenia punctata (NRRL 50757; for example, BroadBand® from BASF Agricultural Specialties (Pty) Ltd., South Africa), strains Bradyrhizobium elkanii SEMIA 5019 (also called 29W) isolated in Rio de Janeiro, Brazil and SEMIA 587 isolated in 1967 in the State of Rio Grande do Sul, from an area previously inoculated with a North American isolate, and used in commercial inoculants since 1968 (Appl. Environ. Microbiol. 73 (8) , 2635, 2007; for example, GELFIX 5 from BASF Agricultural Specialties Ltd., Brazil), B. japonic um 532c isolated from the Wisconsin field in the United States (Nitragin 61A152; Dog. J. Plant. Sci. 70, 661 666, 1990; for example, in Rhizoflo®, Histick®, Hicoat® Super from Ba SF Agricultural Specialties Ltd., Canada), B. japonicum E-109 variant of USDA 138 strain (INTA E109, SEMIA 5085; Eur. J. Soil Biol. 45, 28-35, 2009; Biol. Fertil. Soils 47, 81-89, 2011); B. japonicum strains deposited in SEMIA known from Appl. Environ. Microbiol 73 (8), 2635, 2007: SEMIA 5079 isolated from soil in the Cerrados region, Brazil, by Embrapa-Cerrados used in commercial inoculants since 1992 (CPAC 15; for example, GELFIX 5 or ADHERE 60 from BASF Agricultural Specialties Ltd ., Brazil), B. japonicum SEMIA 5080 obtained under laboratory conditions by Embrapa-Cerrados in Brazil and used in commercial inoculants since 1992, being a natural variant of SEMIA 586 (CB1809) originally isolated in the United States (CPAC 7; for example , GELFIX 5 or ADHERE 60 from BASF Agricultural Specialties Ltd., Brazil); Burkholderia sp. A396 isolated from soil in Nikko, Japan, in 2008 (NRRL 0-50319; WO2013 / 032693; MAj EsTENE®; Marrone Bio Innovations, Inc., United States), Coniothyriumminitans CON / M / 91-08 isolated from rapeseed (WO1996 / 021358; DSM 9660; eg Contans® WG, Intercept® WG from Bayer CropScience AG, Germany), hairpin protein (alpha-beta) (Science 257, 85-88, 1992; eg Messenger ™ or HARP-N -Tek from Plant Health Care plc, UK), Flavobacterium sp. H492 (NRRL Accession No. B-50584); Helicoverpa armigera nucleopolyhedrovirus (HearNPV) (J. Invertebrate Pathol. 107, 112-126, 2011; for example, Helicovex® from Adermatt Biocontrol, Switzerland; Diplomata® from Koppert, Brazil; Vivus® Max from AgBiTech Pty Ltd., Queensland, Australia), Helicoverpa zea single capsid nucleopolyhedrovirus (HzSNPV) (for example, Gemstar® from Certis LLC, USA), Helicoverpa zea nucleopolyhedrovirus ABN-NPV-U (for example, Heligen® from AgBiTech Pty Ltd., Queensland, Australia ), Heterorhabditis bacteriophora (e.g. Nemasys® G from BASF Agricultural Specialties Limited, UK), Isaria fumosorosea Apopka-97 isolated from mealy bugs in gynura in Apopka, Florida, USA (ATCC 20874; Biocontrol Science Technol. 22 (7 ), 747-761, 2012; for example, PFR-97 ™ or PreFeRal® from Certis LLC, USA), Metarhizium anisopliae var. anisopliae F52 also called 275 or V275 isolated from the Austrian apple moth (DSM 3884, ^a T ^c C 90448; for example, Met52® Novozymes Biologicals BioAg Group, Canada), Metschnikowia fructicola 277 isolated from grapes in the central part of Israel (US 6,994,849; NRRL Y-30752; e.g. formerly Shemer® from Agrogreen, Israel), Paecilomyces ilacinus 251 isolated from infected nematode eggs in the Philippines (AGAL 89/030550; WO1991 / 02051; Crop Protection 27, 352-361 , 2008; for example, BioAct® from Bayer CropScience AG, Germany and MeloCon® from Certis, USA), PaeniBacillus alvei NAS6G6 isolated from the rhizosphere of grasses in South Africa at least before 2008 (WO 2014/029697; NRRL O-50755 ; for example, BAC-UP from BASF Agricultural Specialties (Pty) Ltd., South Africa), Pasteuria nishizawae Pn1 isolated from a soybean field in the mid-2000s in Illinois, United States (ATCC SD-5833; Federal Register 76 (22), 5808, February 2, 2011; for example, Clariva ™ PN by Syng enta Crop. Protection, LLC, United States), Penicillium bilaiae (also called P. biiaii) strains ATCC 18309 (= A ^t CC 74319), ATCC 20851 and / or ATCC 22348 (= ATCC 74318) originally isolated from soil in Alberta, Canada (Fertilizer Beef.

39, 97-103, 1994; Dog. J. Plant Sci. 78 (1), 91-102, 1998; US 5,026,417, WO 1995/017806; for example, Jump Start®, Provide® from Novozymes Biologicals BioAg Group, Canada), Reynoutria sachalinensis extract (EP 0307510 B1; for example, Regalia® SC from Marrone Biolnnovations, Davis, CA, USA or Milsana® from BioFa AG, Germany), Steinernema carpocapsae (for example Millenium® from BASF Agricultural Specialties Limited, UK), S. feltiae (for example Nemashield® from BioWorks, Inc., USA; Nemasys® from BASF Agricultural Specialties Limited, UK) , Streptomyces microffavus Nr Rl O-50550 (WO 2014/124369; Bayer CropScience, Germany), Trichoderma asperelloides JM41R isolated from South Africa (NRRL 50759; also known as T. fertil; for example, Trichoplus® from BASF Agricultural Specialties (Pty) Ltd ., South Africa), T. harzianum T-22 also called KRL-AG2 (ATCC 20847; BioControl 57, 687-696, 2012; for example, Plantshield® from BioWorks Inc., USA or SabrEx ™ from Advanced Biological Marketing Inc. , Van Wert, OH, United States).

According to the invention, the solid material (dry matter) of biopesticides (with the exception of oils such as Neem oil) are considered active components (for example, obtained after drying or evaporation of the extraction medium or suspension in case of liquid formulations of microbial pesticides).

In accordance with the present invention, the weight ratios and percentages used herein for a biological extract such as Quillay's extract are based on the total weight of the dry content (solid material) of the extract (s). ) respective (s). The weight ratios of mixtures comprising at least one microbial pesticide in the form of viable microbial cells, including latent forms, can be determined using the amount of CFU of the respective microorganism to calculate the total weight of the respective active component with the following equation : 1 x 1010 CFU equals one gram of total weight of the active component respective. The colony forming unit is a measure of viable microbial cells, particularly fungal and bacterial cells. Furthermore, here "CFU" can also be understood as the number of individual (juvenile) nematodes in the case of nematode biopesticides (entomopathogens), such as Steinernema feltiae.

When using mixtures comprising microbial pesticides in crop protection, application rates preferably range from about 1 x 106 to 5 x 1015 (or more) CFU / ha, preferably from about 1 x 108 to about 1 x 1013 CFU / ha, and even more preferably from about 1x109 to about 1x1012 CFU / ha. In the case of nematodes (entomopathogens) such as microbial pesticides (e.g. Steinernema feltiae), application rates preferably range from 1 x 105 to 1 x 1012 (or more), more preferably 1 x 108 to 1 x 1011, even more preferably 5 x 108 to 1 x 1010 individuals (eg, in the form of eggs, juveniles or any other living stage, preferably in an infectious juvenile stage) per ha. When mixtures comprising microbial pesticides are employed in seed treatment, application rates relative to plant propagation material preferably range from about 1 x 106 to 1 x 1012 (or more) CFU / seed. Preferably, the concentration is from about 1x106 to about 1x109 CFU / seed. In the case of microbial pesticides, application rates with respect to plant propagation material also preferably range from about 1 x 107 to 1 x 1014 (or more) CFU per 100 kg of seed, preferably from 1 x 109 to approximately 1 x 1012 CFU per 100 kg of seed.

Pesticidal mixtures can comprise component C in a synergistically effective amount. The weight ratio of Bacillus amyloliquefaciens and cis-jasmone to component C is usually 10,000: 1 to 1: 10,000, preferably 5000: 1 to 1: 5000, more preferably 1000: 1 to 1: 1000, most preferably 100: 1 to 1: 100, and in particular from 10: 1 to 1:10. The weight ratio of cis-jasmone to component C is typically 10,000: 1 to 1: 10,000, preferably 5000: 1 to 1: 5000, more preferably 1000: 1 to 1: 1000, most preferably 100: 1 to 1: 100, and in particular from 10: 1 to 1:10. The weight ratio of Bacillus amyloliquefaciens to component C is typically 10,000: 1 to 1: 10,000, preferably 5000: 1 to 1: 5000, more preferably 1000: 1 to 1: 1000, most preferably 100: 1 to 1: 100, and in particular from 10: 1 to 1:10. The ratio of Bacillus amyloliquefaciens to component C is typically 1016 CFU: 1 g to 105 CFU: 1 g. In another embodiment, the ratio of Bacillus amyloliquefaciens to component C is 1015 CFU: 1 g to 108 CFU: 1 g. In yet another embodiment, the ratio of Bacillus amyloliquefaciens to component C is 1013 CFU: 1 g to 109 CFU: 1 g. In yet another embodiment, the ratio of Bacillus amyloliquefaciens to component C is from 1013 CFU: 1g to 1010 CFU: 1g. In one embodiment, the pesticidal mixtures further comprise a component C selected from the following groups:

M Insecticides:

M.1 Acetylcholine esterase inhibitors:

M.1A Carbamates: aldicarb, alanicarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, etiofencarb, fenobucarb, formethanate, furathiocarb, isoprocarb, methiocarb, methomofamily, metholpoxycarbicarb, pyroxymethyl, trimethylcarbicarb, pyroxyfamyl, methoxycarbicarbicarb, methomofil, methoxycarbicarbicarb, methomofil, methoxycarbicarbonate , XMC, xylylcarb, and triazamate; Y

M.1B Organophosphates: acefate, azamethiphos, azinphos-ethyl, azinphosmethyl, cadusafos, chlorethoxyphos, chlorfenvinphos, chloromephos, chlorpyrifos, chlorpyrifos-methyl, coumaphos, cyanophos, demeton-S-methyl, diazinon, dichlorvos / dimethylV dimethylP, dichrothoxyphos, Dichlorvos / dimethylV dimethylP , disulfoton, EPN, ethion, ethoprophos, famfur, fenamiphos, fenitrothion, fenthion, fostiazate, heptenophos imitiaphos, isophenphos, isopropyl O- (methoxyamino-phosphoryl) salicylate, isoxathion, malathion, mecarbam, methamidophos, methidation, methamidophos, methidated omethoate, oxydemeton-methyl, parathion, parathion-methyl, phentoate, phorate, fosalone, phosmet, phosphamidon, phoxim, pyrimiphos-methyl, profenophos, propetamfos, protiophos, pyraclophos, pyridaphenthion, quinalphos, sulfotep, tebupphosorimphos, temeclorvinphos thiometon, triazophos, trichlorfon and vamidothion;

M.2 GABA-activated chloride channel antagonists:

M.2A Organochlorine cyclodiene compounds: endosulfan or chlordane; Y

M.2B Fiprole: ethiprole, fipronil, flufiprole, pyrafluprole and pyriprole;

M.3 Sodium channel modulators:

M.3A Pyrethroids: acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin, bifenthrin, bioalethrin, bioalethrin S-cyclopentenyl, bioresmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalpermethrin, alpha-cyhalothrin -cypermethrin, beta-cypermethrin, theta-cypermetria, zeta-cypermethrin, cyphenothrin, deltamethrin, empenthrin, sphenvalerate, etofenprox, phenpropathrin, fenvalerate, flucythrinate, flumethrin, tau-fluvalinate, momofluiprothrin methrothrin, methrothrin methrothrin methrothrin methrothrin methrothrin methrothrin methrothrine , phenothrin, pralethrin, profluthrin, pyrethrin (pyrethrum), resmethrin, silafluofen, tefluthrin, tetramethylfluthrin, tetramethrin, tralomethrin and transfluthrin; and M.3B Sodium channel modulators: DDT and methoxychlor;

M.4 Nicotinic acetylcholine receptor agonists:

M.4A.1 Neonicotinoids: acetamiprid, clothianidinA, cycloxaprid, dinotefuran, imidacloprid, nitenpIram, thiacloprid and thiamethoxam;

M.4A.2 (2E -) - 1 - [(6-Chloropyridin-3-yl) methyl] -N'-nitro-2-pentylidenehydrazine-carboximidamide;

M4.A.3 1 - [(6-Chloropyridin-3-yl) methyl] -7-methyl-8-nitro-5-propoxy-1,2,3,5,6,7-hexahydroimidazo [1,2- a] pyridine; and M.4B Nicotine;

M.5 Allosteric activators of the nicotinic acetylcholine receptor of the spinosyn class: spinosad and spinetoram;

M.6 Activators of chloride channels of the avermectin and milbemycin class: abamectin, emamectin benzoate, ivermectin, lepimectin and milbemectin;

M.7 Juvenile hormone mimics:

M.7A Juvenile Hormone Analogs: Hydroprene, Kinoprene, and Methoprene; Y

M.7B Phenoxycarb and pyriproxyfen;

M.8 Miscellaneous non-specific inhibitors:

M.8A Alkyl halides: methyl bromide and other alkyl halides; Y

M.8B Chloropicrin, sulfuryl fluoride, borax and emetic tartar;

M.9 Selective blockers of homopterana feeding: pymetrozine and flonicamid;

M.10 Mite growth inhibitors: clofentezine, hexythiazox, diflovidazine and ethoxazole;

M.11 Microbial disruptors of the intestinal membranes of the insect: Bacillus thuringiensis, Bacillus sphaericus and the insecticidal proteins that they produce: Bacillus thuringiensis subsp. israelensis, Bacillus sphaericus, Bacillus thuringiensis subsp. aizawai, Bacillus thuringiensis subsp. Kurstaki and Bacillus thuringiensis subsp. tenebrionis, or the Bt culture proteins: Cry1Ab, Cry1Ac, Cry1Fa, Cry2Ab, mCry3A, Cry3Ab, Cry3Bb and Cry34 / 35Ab1;

M.12 Mitochondrial ATP synthase inhibitors:

M.12A Diaphentiuron, and organicin miticides: azocyclotin, cyhexatin and fenbutatin oxide; Y

M.12B Propargite and tetradiphon;

M.13 Oxidative phosphorylation decouplers through proton gradient disruption: chlorfenapir, DNOC, and sulfluramide;

M.14 Nicotinic acetylcholine receptor channel blockers: bensultap, cartap hydrochloride, thiocyclam, and tiosultap sodium;

M.15 Type 0 chitin biosynthesis inhibitors: bistrifluron, chlorfluazuron, diflubenzuron, flucicloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron and triflumuron;

M.16 Type 1 chitin biosynthesis inhibitors: buprofezin;

M.17 Molting disruptors: chromazine;

M.18 Ecdyson receptor agonists: methoxyphenozide, tebufenozide, halofenozide, fufenozide, or chromafenozide; M.19 Octopamine receptor agonists: amitraz;

M.20 Inhibitors of electron transport of mitochondrial complex III: hydramethylnon, acequinocyl and fluacripirim;

M.21 Inhibitors of electron transport of mitochondrial complex I:

M.21A METI acaricides and insecticides: fenazaquin, fenpyroximate, pyrimidiphene, pyridaben, tebufenpyrad and tolfenpyrad; Y

M.21B Rotenone;

M.22 Voltage-gated sodium channel blockers:

M.22A Indoxacarb;

M.22B Metaflumizone;

M.22B.1 2- [2- (4-Cyanophenyl) -1- [3- (trifluoromethyl) phenyl] ethylidene] -N- [4- (difluoromethoxy) phenyl] -hydrazinecarboxamide;

M.22B.2 N- (3-Chloro-2-methylphenyl) -2 - [(4-chlorophenyl) [4- [methyl (methylsulfonyl) amino] phenyl] methylene] -hydrazinecarboxamide;

M.23 Acetyl CoA carboxylase inhibitors of the class of tetronic and tetramic acid derivatives: spirodiclofen, spiromesifene and spirotetramat;

M.24 Inhibitors of electron transport of mitochondrial complex IV:

M.24A Phosphorous compounds: aluminum phosphide, calcium phosphide, phosphine and zinc phosphide; Y

M.24B Cyanide;

M.25 Mitochondrial complex II electron transport inhibitors of the class of beta-acetonitrile derivatives: Cenopirafen and Cyflumetofen;

M.28 Diamide class ryanodine receptor modulators: flubendiamide, chlorantraniliprole (rynaxypyr®), cyazypyr® *, tetranyliprole, and the phthalamide compounds;

M.28.1 (R) -3-Chloro-N1- {2-methyl-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] phenyl} -N2- (1-methyl-2- methylsulfonylethyl) phthalamide;

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; M.28.3 3-bromo-N- {2-bromo-4-chloro-6 - [(1-cyclopropylethyl) carbamoyl] phenyl} -1- (3-chlorpyridin-2-yl) -1H-pyrazole-5-carboxamide (proposed ISO name: cyclaniliprole);

M.28.4 methyl-2- [3,5-dibromo-2- (3-chlorpyridin-2-yl) -1H-pyrazol-5-yl] carbonyl} amino) benzoyl] -1,2-dimethylhydrazinecarboxylate;

M.28.5a N- [4,6-dichloro-2 - [(diethyl-lambda-4-sulfanylidene) carbamoyl] -phenyl] -2- (3-chloro-2-pyridyl) -5- (trifluoromethyl) pyrazole- 3-carboxamide;

M.28.5b N- [4-chloro-2 - [(diethyl-lambda-4-sulfanylidene) carbamoyl] -6-methyl-phenyl] -2- (3-chloro-2-pyridyl) -5- (trifluoromethyl) pyrazole-3-carboxamide;

M.28.5c N- [4-chloro-2 - [(di-2-propyl-lambda-4-sulfanylidene) carbamoyl] -6-methyl-phenyl] -2- (3-chloro-2-pyridyl) -5 - (trifluoromethyl) pyrazole-3-carboxamide;

M.28.5d N- [4,6-dichloro-2 - [(di-2-propyl-lambda-4-sulfanylidene) carbamoyl] -phenyl] -2- (3-chloro-2-pyridyl) -5- ( trifluoromethyl) pyrazole-3-carboxamide;

M.28.5h N- [4,6-dibromo-2 - [(diethyl-lambda-4-sulfanylidene) carbamoyl] -phenyl] -2- (3-chloro-2-pyridyl) -5- (trifluoromethyl) pyrazole- 3-carboxamide;

M.28.5i N- [2- (5-Amino-1,3,4-thiadiazol-2-yl) -4-chloro-6-methylphenyl] -3-bromo-1- (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] carbonyl] phenyl] -1H -pyrazole-5-carboxamide;

M.28.5k 3-Bromo-N- [2,4-dichloro-6- (methylcarbamoyl) phenyl] -1- (3,5-dichloro-2-pyridyl) -1H-pyrazole-5-carboxamide;

M.28.5I N- [4-Chloro-2 - [[(1,1-dimethylethyl) amino] carbonyl] -6-methylphenyl] -1- (3-chloro-2-pyridinyl) -3- (fluoromethoxy) - 1H-pyrazole-5-carboxamide; Y

M.28.6 Cylodiamide;

M.29. insecticidal active compounds of unknown or uncertain mode of action: afidopiropen, afoxolaner, azadirachtin, amidoflumet, benzoximate, bifenazate, broflanilide, bromopropylate, quinomethionate, crolite, dichloromezothiaz, dicofol, flufenerim, flomethoupine, fluransulfone, fluransulfone, fluransulfone, fluransulfone, methoxadiazone, piperonyl butoxide, pyroflubumide, pyridylyl, pyrifluquinazon, sulfoxaflor, thioxazafen, and triflumezopyrim;

M.29.3 11- (4-chloro-2,6-dimethylphenyl) -12-hydroxy-1,4-dioxa-9-azadispiro [4.2.4.2] -tetradec-11-en-10-one;

M.29.4 3- (4'-fluoro-2,4-dimethylbiphenyl-3-yl) -4-hydroxy-8-oxa-1-azaspiro [4.5] dec-3-en-2-one;

M.29.5 1- [2-fluoro-4-methyl-5 - [(2,2,2-trifluoroethyl) sulfinyl] phenyl] -3- (trifluoromethyl) -1H-1,2,4-triazol-5-amine

and assets based on Bacillus firmus (Votive, I-1582); Y

M.29.6a (E / Z) -N- [1 - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2,2-trifluoroacetamide;

M.29.6b (E / Z) -N- [1 - [(6-chloro-5-fluoro-3-pyridyl) methyl] -2-pyridylidene] -2,2,2-trifluoro-acetamide;

M.29.6c (E / Z) -2,2,2-trifluoro-N- [1 - [(6-fluoro-3-pyridyl) methyl] -2-pyridylidene] acetamide;

M.29.6d (E / Z) -N- [1 - [(6-bromo-3-pyridyl) methyl] -2-pyridylidene] -2,2,2-trifluoroacetamide;

M.29.6e (E / Z) -N- [1- [1- (6-chloro-3-pyridyl) ethyl] 2-pyridylidene] 2,2,2-trifluoro-acetamide;

M.29.6f (E / Z) -N- [1 - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2-difluoro-acetamide;

M.29.6g (E / Z) -2-chloro-N- [1 - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2-difluoro-acetamide;

M.29.6h (E / Z) -N- [1 - [(2-chloropyrimidin-5-yl) methyl] -2-pyridylidene] -2,2,2-trifluoroacetamide;

M.29.6i (E / Z) -N- [1 - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2,3,3,3-pentafluoro-propanamide);

M.29.6j N- [1 - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2,2-trifluoro-thioacetamide; Y

M.29.6k N- [1 - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2,2-trifluoro-N'-isopropyl-acetamidine;

M.29.8 Fluazaindolizine;

M.29.9a 4- [5- (3,5-dichlorophenyl) -5- (trifluoromethyl) -4H-isoxazol-3-yl] -2-methyl-N- (1-oxothietan-3-yl) benzamide; and M.29.9b Fluxamethamide;

M.29.10 5- [3- [2,6-dichloro-4- (3,3-dichloroallyloxy) phenoxy] propoxy] -1H-pyrazole;

M.29.11b 3- (benzoylmethylamino) -N- [2-bromo-4- [1,2,2,3,3,3-hexafluoro-1- (trifluoromethyl) propyl] -6- (trifluoromethyl) phenyl] - 2-fluoro-benzamide;

M.29.11c 3- (benzoylmethylamino) -2-fluoro-N- [2-iodo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- (trifluoromethyl) phenyl] - benzamide;

M.29.11d N- [3 - [[[2-iodo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- (trifluoromethyl) phenyl] amino] carbonyl] phenyl] -N-methyl-benzamide;

M.29.11e N- [3 - [[[2-bromo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- (trifluoromethyl) phenyl] amino] carbonyl] -2 -fluorophenyl] -4-fluoro-N-methyl-benzamide;

M.29.11f 4-fluoro-N- [2-fluoro-3 - [[[2-iodo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- (trifluoromethyl) phenyl] amino] carbonyl] phenyl] -N-methyl-benzamide;

M.29.11g 3-fluoro-N- [2-fluoro-3 - [[[2-iodo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- (trifluoromethyl) phenyl] amino] carbonyl] phenyl] -N-methyl-benzamide;

M.29.11h 2-chloro-N- [3 - [[[2-iodo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- (trifluoromethyl) phenyl] amino] carbonyl] phenyl] -3-pyridinecarboxamide;

M.29.11 i 4-cyano-N- [2-cyano-5 - [[2,6-dibromo-4- [1,2,2,3,3,3-hexafluoro-1- (trifluoromethyl) -propyl]] phenyl] carbamoyl] phenyl] -2-methyl-benzamide;

M.29.11j 4-cyano-3 - [(4-cyano-2-methyl-benzoyl) amino] -N- [2,6-dichloro-4- [1,2,2,3,3,3-hexafluoro -1- (trifluoromethyl) propyl] phenyl] -2-fluoro-benzamide;

M.29.11k N- [5 - [[2-chloro-6-cyano-4- [1,2,2,3,3,3-hexafluoro-1- (trifluoromethyl) propyl] -phenyl] carbamoyl] -2 -cyanophenyl] -4-cyano-2-methyl-benzamide;

M.29.111 N- [5 - [[2-bromo-6-chloro-4- [2,2,2-trifluoro-1-hydroxy-1- (trifluoromethyl) ethyl] -phenyl] carbamoyl] -2-cyano- phenyl] -4-cyano-2-methyl-benzamide;

M.29.11m N- [5 - [[2-bromo-6-chloro-4- [1,2,2,3,3,3-hexafluoro-1- (trifluoromethyl) -propyl] phenyl] carbamoyl] -2 -cyanophenyl] -4-cyano-2-methyl-benzamide;

M.29.11n 4-cyano-N- [2-cyano-5 - [[2,6-dichloro-4- [1,2,2,3,3,3-hexafluoro-1- (trifluoromethyl) -propyl] phenyl] carbamoyl] phenyl] -2-methyl-benzamide;

M.29.11o 4-cyano-N- [2-cyano-5 - [[2,6-dichloro-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] phenyl] carbamoyl] phenyl ] -2-methyl-benzamide;

M.29.11p N- [5 - [[2-bromo-6-chloro-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] phenyl] -carbamoyl] -2-cyano-phenyl ] -4-cyano-2-methyl-benzamide;

M.29.12a 2- (1,3-Dioxan-2-yl) -6- [2- (3-pyridinyl) -5-thiazolyl] -pyridine;

M.29.12b 2- [6- [2- (5-Fluoro-3-pyridinyl) -5-thiazolyl] -2-pyridinyl] -pyrimidine;

M.29.12c 2- [6- [2- (3-pyridinyl) -5-thiazolyl] -2-pyridinyl] -pyrimidine;

M.29.12d N-methylsulfonyl-6- [2- 3-pyridyl) iazol-5-yl] iridine-2-carboxamide;

M.29.12e N-methylsulfonyl-6- [2- (3-pyridyl) thiazol-5-yl] pyridine-2-carboxamide;

M.29.12f N-Ethyl-N- [4-methyl-2- (3-pyridyl) thiazol-5-yl] -3-methylthio-propanamide;

M.29.12g N-Methyl-N- [4-methyl-2- (3-pyridyl) thiazol-5-yl] -3-methylthio-propanamide;

M.29.12h N, 2-Dimethyl-N- [4-methyl-2- (3-pyridyl) thiazol-5-yl] -3-methylthio-propanamide;

M.29.12i N-Ethyl-2-methyl-N- [4-methyl-2- (3-pyridyl) thiazol-5-yl] -3-methylthio-propanamide;

M.29.12j N- [4-chloro-2- (3-pyridyl) thiazol-5-yl] -N-ethyl-2-methyl-3-methylthio-propanamide;

M.29.12k N- [4-chloro-2- (3-pyridyl) thiazol-5-yl] -N, 2-dimethyl-3-methylthio-propanamide;

M.29.12l N- [4-chloro-2- (3-pyridyl) thiazol-5-yl] -N-methyl-3-methylthio-propanamide;

M.29.12m N- [4-chloro-2- (3-pyridyl) thiazol-5-yl] -N-ethyl-3-methylthio-propanamide; or the compounds

M.29.14a 1 - [(6-Chloro-3-pyridinyl) methyl] -1,2,3,5,6,7-hexahydro-5-methoxy-7-methyl-8-nitro-imidazo [1,2 -a] pyridine; M.29.14b 1 - [(6-Chloropyridin-3-yl) methyl] -7-methyl-8-nitro-1,2,3,5,6,7-hexahydroimidazo [1,2-a] pyridin-5 -ol;

M.29.16a 1-isopropyl-N, 5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; or

M.29.16b 1- (1,2-dimethylpropyl) -N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide;

M.29.16c N, 5-dimethyl-N-pyridazin-4-yl-1 - 2,2,2-trifluoro-1-methyl-ethyl) pyrazole-4-carboxamide;

M.29.16d 1- [1- (1-cyanocyclopropyl) ethyl] -N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide;

M.29.16e N-ethyl-1- (2-fluoro-1-methyl-propyl) -5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide;

M.29.16f 1- (1,2-dimethylpropyl) -N, 5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide;

M.29.16g 1- [1- (1-cyanocyclopropyl) ethyl] -N, 5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide;

M.29.16h N-methyl-1- (2-fluoro-1-methyl-propyl] -5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide;

M.29.16i 1- (4,4-difluorocyclohexyl) -N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; Y

M.29.16j 1- (4,4-difluorocyclohexyl) -N, 5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide;

M.29.17a N- (1-methylethyl) -2- (3-pyridinyl) -2H-indazole-4-carboxamide;

M.29.17b N-cyclopropyl-2- (3-pyridinyl) -2H-indazole-4-carboxamide;

M.29.17c N-cyclohexyl-2- (3-pyridinyl) -2H-indazole-4-carboxamide;

M.29.17d 2- (3-pyridinyl) -N- (2,2,2-trifluoroethyl) -2H-indazole-4-carboxamide;

M.29.17e 2- (3-pyridinyl) -N - [(tetrahydro-2-furanyl) methyl] -2H-indazole-5-carboxamide;

M.29.17f methyl 2 - [[2- (3-pyridinyl) -2H-indazol-5-yl] carbonyl] hydrazinecarboxylate;

M.29.17g N - [(2,2-difluorocyclopropyl) methyl] -2- (3-pyridinyl) -2H-indazole-5-carboxamide;

M.29.17h N- (2,2-difluoropropyl) -2- (3-pyridinyl) -2H-indazole-5-carboxamide;

M.29.17i 2- (3-pyridinyl) -N- (2-pyrimidinylmethyl) 2H-indazole-5-carboxamide; Y

M.29.17j N - [(5-methyl-2-pyrazinyl) methyl] -2- (3-pyridinyl) -2H-indazole-5-carboxamide;

M.29.18a N- [3-chloro-1- (3-pyridyl) pyrazol-4-yl] -N-ethyl-3- (3,3,3-trifluoropropylsulfanyl) -propanamide;

M.29.18b N- [3-chloro-1- (3-pyridyl) pyrazol-4-yl] -N-ethyl-3- (3,3,3-trifluoropropylsulfinyl) -propanamide;

M.29.18c N- [3-chloro-1- (3-pyridyl) pyrazol-4-yl] -3 - [(2,2-difluorocyclopropyl) -methylsulfanyl] -N-ethyl-propanamide; and M.29.18d N- [3-chloro-1- (3-pyridyl) pyrazol-4-yl] -3 - [(2,2-difluorocyclopropyl) -methylsulfinyl] -N-ethyl-propanamide;

M.29.19 Sarolaner;

M.29.20 Lotilaner;

L Biopesticides:

L.1 Microbial pesticides with fungicidal, bactericidal, viricidal and / or activating plant defense activity: Ampelomyces quisqualis, Aspergillus flavus, Aureobasidium pullulans, Bacillus altitudinis, B. megaterium, B. mojavensis, B. mycoides, B. simplex, B. solisalsi, B. subtilis, Candida oieophiia, C. saitoana, Clavibacter michiganensis (bacteriophages), Coniothyrium minitans, Cryphonectria parasitica, Cryptococcus albidus, Dilophosphora alopecuri, Fusarium oxysporum, Clonostachys rosea f. catenulate (Gliocladium catenulatum also called), Gliocladium roseum, Lysobacter antibioticus, L. enzymogenes, Metschnikowia fructicola, Microdochium dimerum, Microsphaeropsis ochracea, Muscodor albus, Paenibacillus polymyxa, Pantoea vagans, Penicillium Bilaiae, Phlebiopsis gigantea, Pseudomonas sp., Pseudomonas chloraphis, Pseudozyma flocculosa, Pichia anomala, Pythium oligandrum, Sphaerodes mycoparasitica, Streptomyces griseoviridis, S. lydicus, S. violaceusniger, Talaromyces flavus, T. asperellum, T. atroviride, T. fertile, T. gamsii, T. harmatum, T. harzianum, T polysporum, T. stromaticum, T. virens, T. viride, Typhula phacorrhiza, Ulocladium oudemansii, Verticillium dahlia, and zucchini yellow mosaic virus (avirulent strain);

L.2 Biochemical pesticides with fungicidal, bactericidal, viricidal and / or vegetal defense activating activity: hairpin protein and Reynoutria sachalinensis extract;

L.3 Microbial pesticides with insecticidal, acaricidal, molluscid and / or nematicidal activity: Agrobacterium radiobacter, Bacillus cereus, B. firmus, B. thuringiensis, B. thuringiensis ssp. aizawai, B. t. ssp. israelensis, B. t. ssp. galleriae, B. t. ssp. tenebrionis, Beauveria bassiana, B. brongniartii, Burkholderia spp., Chromobacterium subtsugae, Cydia pomonella granulovirus (CpGV), Cryptophlebia leucotreta granulovirus (CrleGV), Flavobacterium spp., Helicoverpa armigera nucleopolihedrovirus (Helicoverpa polyhedrovirus) Nucleopolihedrovirus (Helicoverpa Vhedrovirus) ), Helicoverpa zea single capsid nucleopolyhedrovirus (HzSNPV), Heterorhabditis bacteriophora, Isaria fumosorosea, Lecanicillium longisporum, L. muscarium, Metarhizium anisopliae, Metarhizium anisopliae var. anisopliae, M. anisopliae var. acridum, Nomuraea rileyi, Paecilomyces fumosoroseus, P. lilacinus, Paenibacillus popilliae, Pasteuria spp., P. nishizawae, P. penetrans, P. ramosa, P. thornea, P. Usgae, Pseudomonas fluorescens, Spodoptera littoralis nucleopolyhedrovirus (SpliNPV), Steinernema carpocapsae, S. feltiae, S. kraussei, Streptomyces galbus, and S. microflavus;

L.4 Biochemical pesticides with insecticidal, acaricidal, molluscid, pheromone and / or nematicidal activity: L-carvone, citral, (E, Z) -7,9-dodecadien-1-yl acetate, ethyl formate, (E, Z ) Ethyl -2,4-decadienoate (pear ester), (Z, Z, E) -7,11,13-hexadecatrienal, heptyl butyrate, isopropyl myristate, lavender lavender, 2-methyl 1-butanol, methyl eugenol, (E, Z) -2,13-octadecadien-1-ol, (E, Z) -2,13-octadecadien-1-ol acetate, (E, Z) -3,13-octadecadien-1- ol, R-1-octen-3-ol, pentatermanone, (E, Z, Z) -3,8,11-tetradecatrienyl acetate, (Z, E) -9,12-tetradecadien-1-yl acetate, Z-7-tetradecen-2-one, Z-9-tetradecen-1-yl acetate, Z-11-tetradecenal, Z-11-tetradecen-1-ol, Chenopodium ambrosiodes extract, Neem oil and Quillay extract ;

L.5 Microbial pesticides with plant stress reduction, plant growth regulator, plant growth promoting activity and / or yield enhancement: A. lipoferum, A. irakense, A. halopraeferens, B. elkanii , B. liaoningense, B. lupini, Delfíia acidovorans, Glomus intraradices, Mesorhizobium spp., Rhizobium leguminosarum bv. phaseoli, R. l. bv. trifolii, R. l. bv. viciae, R. tropici, and Sinorhizobium meliloti;

F Fungicides:

F.I Respiratory inhibitors

F.I1 Complex III inhibitors at the Qo site: azoxystrobin, cumethoxystrobin, coumoxystrobin, dimoxystrobin, enestroburin, phenaminstrobin, phenoxy-strobin / fluphenoxystrobin, fluoxastrobin, cresoxim-methyl, manrazdestrobin, pyraxystrobin, methoxystrobin, metho-minostrobin, pyraxystrobin, methoxystrobin pyroxystrobin, trifloxystrobin, 2- (2- (3- (2,6-dichlorophenyl) -1-methyl-allylidene-aminoxymethyl) -phenyl) -2-methoxyimino-N-methyl-acetamide, pyribencarb, triclopyricarb / chlorodincarb, famoxadone and phenamidone, methyl-N- [2 - [(1,4-dimethyl-5-phenyl-pyrazol-3-yl) oxylmethyl] phenyl] -N-methoxy-carbamate, 1- [3-chloro-2 - [[1 - (4-chlorophenyl) -1H-pyrazol-3-yl] oxymethyl] phenyl] -4-methyl-tetrazol-5-one, 1- [3-bromo-2 - [[1- (4-chlorophenyl) pyrazole- 3-yl] oxymethyl] phenyl] -4-methyl-tetrazol-5-one, 1- [2 - [[1- (4-chlorophenyl) pyrazol-3-yl] oxymethyl] -3-methyl-phenyl] -4 -methyl-tetrazol-5-one, 1- [2 - [[1- (4-chlorophenyl) pyrazol-3-yl] oxymethyl] -3-fluoro-phenyl] -4-methyl-tetrazol-5-one, 1 - [2 - [[1 - (2,4-dichlorophenyl) pyrazol-3-yl] oxymethyl] -3-fluo ro-phenyl] -4-methyl-tetrazol-5-one, 1- [2 - [[4- (4-chlorophenyl) thiazol-2-yl] oxymethyl] -3-methylphenyl] -4-methyl-tetrazole-5 -one, 1- [3-chloro-2 - [[4- (p-tolyl) thiazol-2-yl] oxymethyl] phenyl] -4-methyl-tetrazol-5-one, 1- [3-cyclopropyl-2 - [[2-methyl-4- (1-methylpyrazol-3-yl) phenoxy] methyl] phenyl] -4-methyl-tetrazol-5-one, 1- [3- (difluoromethoxy) -2 - [[2- methyl-4- (1-methylpyrazol-3-yl) phenoxy] methyl] phenyl] -4-methyl-tetrazol-5-one, 1-methyl-4- [3-methyl-2 - [[2-methyl-4 - (1-methylpyrazol-3-yl) phenoxy] methyl] phenyl] tetrazol-5-one, 1-methyl-4- [3-methyl-2 - [[1- [3- (trifluoromethyl) phenyl] -ethylideneamino] oxymethyl] phenyl] tetrazol-5-one, (Z, 2E) -5- [1- (2,4-dichlorophenyl) pyrazol-3-yl] oxy-2-methoxyimino-N, 3-dimethyl-pent-3- enamide, (Z, 2E) -5- [1- (4-chlorophenyl) pyrazol-3-yl] oxy-2-methoxyimino-N, 3-dimethyl-pent-3-enamide and (Z, 2E) -5- [1- (4-chloro-2-fluoro-phenyl) pyrazol-3-yl] oxy-2-methoxyimino-N, 3-dimethyl-pent-3-enamide;

F.I2 Complex III inhibitors at the Qi site: fenpicoxamide, ciazofamide, amisulbrom, 2-methylpropanoate [(3S, 6S, 7R, 8R) -8-benzyl-3 - [(3-acetoxy-4-methoxy-pyridine -2-carbonyl) amino] -6-methyl-4,9-dioxo-1,5-dioxonan-7-yl], [(3S, 6S, 7R, 8R) -8-benzyl-3- [[3- (acetoxymethoxy) -4-methoxy-pyridine-2-carbonyl] amino] -6-methyl-4,9-dioxo-1,5-dioxonan-7-yl], [(3S, 6S, 7R, 8R) -8-benzyl-3 - [(3-isobutoxycarbonyloxy-4-methoxy-pyridine-2-carbonyl) amino] -6-methyl-4,9-dioxo-1,5-dioxonan-7- yl], [(3S, 6S, 7R, 8R) -8-benzyl-3 - [[3- (1,3-benzodioxol-5-ylmethoxy) -4-methoxy-pyridine-2-carbonyl] 2-methylpropanoate amino] -6-methyl-4,9-dioxo-1,5-dioxonan-7-yl]; (3S, 6S, 7R, 8R) -3 - [[(3-hydroxy-4-methoxy-2-pyridinyl) carbonyl] amino] -6-methyl-4,9-dioxo-8- (phenylmethyl ) -1,5-dioxonan-7-yl and (3S, 6S, 7R, 8R) -8-benzyl-3- [3 - [(isobutyryloxy) methoxy] -4-methoxypicolinamido] -6-methyl-4 isobutyrate , 9-dioxo-1,5-dioxonan-7-yl;

F.I3 Complex II inhibitors: pidiflumetofen, benodanyl, benzovindiflupir, bixafen, boscalid, carboxin, fenfuram, fluopyram, flutolanil, fluxapyroxad, furametpyr, isofetamid, isopyrazam, mepronil, oxycarboxin, sedative, petalamiophlufluidene, petalamiophlufenuide (4'-trifluoromethylthiobiphenyl-2-yl) -3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxamide, N- (2- (1,3,3-trimethyl-butyl) -phenyl) -1,3 -dimethyl-5-fluoro-1H-pyrazole-4-carboxamide, 3- (difluoromethyl) -1-methyl-N- (1,1,3-trimethylindan-4-yl) pyrazole-4-carboxamide, 3- (trifluoromethyl ) -1-methyl-N- (1,1,3-trimethylindan-4-yl) pyrazole-4-carboxamide, 1,3-dimethyl-N- (1,1,3-trimethylindan-4-yl) pyrazole- 4-carboxamide, 3- (trifluoromethyl) -1,5-dimethyl-N- (1,1,3-trimethylindan-4-yl) pyrazole-4-carboxamide, 1,3,5-trimethyl-N- (1, 1,3-trimethylindan-4-yl) pyrazole-4-carboxamide, N- (7-fluoro-1,1,3-trimethyl-indan-4-yl) -1,3-dimethyl-pyrazole-4-carboxamide and N- [2- (2,4-dichlorophenyl) -2-methoxy-1-methyl-ethyl] -3- (difluoromethyl) -1-methyl-pyrazole-4-carboxamide;

F.I4 Other respiration inhibitors: Diflumethorim, (5,8-difluoroquinazolin-4-yl) - {2- [2-fluoro-4- (4-trifluoromethylpyridin-2-yloxy) -phenyl] -ethyl} -amine ; nitrophenyl derivatives: binapacryl, dinobuton, dinocap, fluazinam, ferimzonA; organometallic compounds: fenthin acetate, fenthin chloride, and fenthin hydroxide; Amethoctradine; and silthofam;

F.II Inhibitors of sterol biosynthesis:

F.II1 Demethylase C14 inhibitors: triazoles: azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imconaluconazole, mecloconazole, ipconazole, mecloconazole, mecloconazole, ipconazole, mconazole, mecloconazole, mecloconazole paclobutrazol, penconazole, propiconazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole, uniconazole, 1- [rel- (2S; 3R) -3- (2-chlorophenyl) -2- (2,4-difluorophenyl) -oxyranylmethyl] -5-thiocyanate-1H- [1,2,4] triazolo, 2- [rel- (2S; 3R) -3- (2-chlorophenyl) -2- (2,4-difluorophenyl) -oxyranyl- methyl] -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- (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-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- (trifluoro romethyl) phenyl] -3-methyl-1- (1,2,4-triazol-1-yl) butan-2-ol, 2- [4- (4-chlorophenoxy) -2- (trifluoromethyl) -phenyl] - 1- (1,2,4-triazol-1-yl) propan-2-ol, 2- [2-chloro-4- (4-chlorophenoxy) phenyl] -3-methyl-1- (1,2,4 -triazol-1-yl) butan-2-ol, 2- [4- (4-chlorophenoxy) -2- (trifluoromethyl) -phenyl] -1- (1,2,4-triazol-1-yl) pentan- 2-ol, 2- [4- (4-fluorophenoxy) -2- (trifluoromethyl) -phenyl] -1- (1,2,4-triazol-1-yl) propan-2-ol, 2- [2- chloro-4- (4-chlorophenoxy) phenyl] -1- (1,2,4-triazol-1-yl) pent-3-in-2-ol; imidazoles: imazalil, pefurazoate, prochloraz, triflumizole;

pyrimidines, pyridines, and piperazines: fenarimol, nuarimol, pyrifenox, triforine, and [3- (4-chloro-2-fluoro-phenyl) -5- (2,4-difluorophenyl) isoxazol-4-yl] - (3-pyridyl) methanol;

F.II2 Delta14-reductase inhibitors: aldimorf, dodemorf, dodemorf-acetate, fenpropimorph, tridemorph, fenpropidine, piperaline and spiroxamine;

F.II3 3-keto reductase inhibitors: fenhexamide;

F.III Inhibitors of nucleic acid synthesis

F.III1 Phenylamides or acylamino acid fungicides: benalaxyl, benalaxyl-M, kiralaxyl, metalaxyl, metalaxyl-M (mephenoxam), ofurace and oxadixyl;

F.III2 Others: hymexazole, octilinone, oxolinic acid, bupirimate, 5-fluorocytosine, 5-fluoro-2- (p-tolylmethoxy) pyrimidin-4-amine and 5-fluoro-2- (4-fluorophenyl-methoxy) pyrimidine- 4-amine;

F.IV Inhibitors of cell division and the cytoskeleton.

F.IV1 Tubulin inhibitors of the benzimidazole and thiophanate class: benomyl, carbendazim, fuberidazole, thiabendazole and thiophanate-methyl; triazolopyrimidines: 5-chloro-7- (4-methylpiperidin-1-yl) -6- (2,4,6-trifluorophenyl) - [1,2,4] triazolo [1,5-a] pyrimidine; Y

F.IV2 Other inhibitors of cell division: dietofencarb, etaboxam, pencycuron, fluopicolide, zoxamide, metrafenone, pyrophenone;

F.V Amino Acid and Protein Synthesis Inhibitors:

F.V1 Inhibitors of methionine synthesis of the class of anilino-pyrimidines: cyprodinil, mepanipyrim and pyrimethanil; Y

F.V2 Protein synthesis inhibitors: blasticidin-S, kasugamycin, kasugamycin hydrochloride-hydrate, mildiomycin, streptomycin, oxytetracycline, polyoxin, and validamycin A;

F.VI Inhibitors of signal transduction:

F.VI1 MAP / histidine kinase inhibitors: fluoroimide, iprodione, procymidone, vinclozolin, fenpiclonil and fludioxonil; Y

F.VI2 G protein inhibitors: quinoxyfen;

F.VII Inhibitors of lipid and membrane synthesis:

F.VII1 Inhibitors of phospholipid biosynthesis: edifenfos, iprobenfos, pyrazofos, isoprothiolane;

F.VII2 lipid peroxidation: dichloran, quintacene, technazene, tolclofos-methyl, biphenyl, chloroneb, and etridiazole;

F.VII3 Phospholipid biosynthesis and cell wall deposition: dimethomorph, flumorf, mandipropamid, pirimorf, benthiavalicarb, iprovalicarb, valifenalate and (4-fluorophenyl) acid ester N- (1- (1- (4-cyano-phenyl) ethanesulfonyl) -but-2-yl) carbamic;

F.VII4 compounds that affect the permeability of the cell membrane and fatty acids: propamocarb; and F.VII5 Fatty acid amide hydrolase inhibitors: oxathiapiproline, 2- {3- [2- (1 - {[3,5-bis (di-fluoromethyl-1H-pyrazol-1-yl] acetyl) phenylmethanesulfonate} piperidin-4-yl) -1,3-thiazol-4-yl] -4,5-dihydro-1,2-oxazol-5-yl}, 2- {3- [2- (1 - {[3, 5-bis (difluoromethyl) -1H-pyrazol-1-yl] acetyl} piperidin-4-yl) and 1,3-thiazol-4-yl] -4,5-dihydro-1,2-oxazol-5 methanesulfonate -yl} -3-chlorophenyl;

F.VIII Inhibitors with multisite action:

F.VIII1 Active inorganic substances: Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate and sulfur;

F.VIII2 Thio and dithiocarbamates: ferbam, mancozeb, maneb, metam, metiram, propineb, thiram, zineb and ziram;

F.VIII3 Organochlorine compounds of the class of phthalimides, sulfonamides and chloronitriles: anilazine, chlorothalonil, captafol, captan, folpet, dichlorofluanide, dichlorophene, hexachlorobenzene, pentachlorophenols and their salts, phthalide, tolylfluanide and N- (4-chloro -phenyl) -N-ethyl-4-methyl-benzenesulfonamide; Y

F.VIII4 Guanidines and others: guanidine, dodyne, dodyne free base, guazatine, guazatine acetate, iminoctadine, i-minoctadine-triacetate, iminoctadin-tris (albesylate), dithianon and 2,6-dimethyl-1H, 5H- [1 , 4] dithiino [2,3-c: 5,6-c '] dipyrrole-1,3,5,7 (2H, 6H) -tetraone;

F.IX Inhibitors of cell wall synthesis:

F.IX1 Inhibitors of glucan synthesis: validamycin and polyoxin B;

F.IX2 Melanin synthesis inhibitors: pyroquilon, tricyclazole, carpropamid, dicyclomet and phenoxanil;

FX Plant defense inducers:

F.X1 Acibenzolar-S-methyl, probenazole, isothianyl, thiadinyl, prohexadione-calcium;

F.X2 Phosphonates: Fosethyl, Phosetylaluminum, Phosphorous acid and their salts; potassium or sodium bicarbonate; Y

F.XI Unknown mode of action: bronopol, quinomethionate, cyflufenamid, cymoxanil, dazomet, debacarb, diclomezine, diphenzoquat, diphenzoquat-methylsulfate, diphenylamine, phenpyrazamine, flumethover, flusulfamide, flutianil, metasulfocarb, nitrite-isopropyl proprol, nitrate-isopropyl proprol oxine-copper, proquinazid, tebufloquin, tecloftalam, triazoxide, 2-butoxy-6-iodo-3-propylchrome-4-one, 2- [3,5-bis (difluoromethyl) -1H-pyrazol-1-yl] -1 - [4- (4- {5- [2- (prop-2-yn-1-yloxy) phenyl] -4,5-dihydro-1,2-oxazol-3-yl} -1,3-thiazol- 2-yl) piperidin-1-yl] ethanone, 2- [3,5-bis (difluoromethyl) -1H-pyrazol-1-yl] -1 - [4- (4- {5- [2-fluoro-6 - (prop-2-yn-1 -yloxy) phenyl] -4,5-dihydro-1,2-oxazol-3-yl} -1,3-thiazol-2-yl) piperidin-1-yl] ethanone, 2- [3,5-bis (difluoromethyl) -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} -1,3-thiazol-2-yl) piperidin-1-yl] ethanone, N- (cyclopropylmethoxyimino- (6-difluoro-methoxy- 2,3-Difluoro-phenyl) -methyl) -2-phenyl acetamide, N '- (4- (4-chloro-3-trifluoromethyl-fe noxy) -2,5-dimethyl-phenyl) -N-ethyl-N-methylformamidine, N '- (4- (4-fluoro-3-trifluoromethyl-phenoxy) -2,5-dimethyl-phenyl) -N-ethyl -N-methylformamidine, N '- (2-methyl-5-trifluoromethyl-4- (3-trimethylsilanyl-propoxy) -phenyl) -N-ethyl-N-methylformamidine, N' - (5-difluoromethyl-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-chloro-phenyl) -2,3-dimethyl-isoxazolidine-3-yl] - pyridine (pyrisoxazole), N- (6-methoxy-pyridin-3-yl) cyclopropanecarboxylic acid amide, 5-chloro-1- (4,6-dimethoxy-pyrimidin-2-yl) -2-methyl-1H-benzoimidazole , 2- (4-Chloro-phenyl) -N- [4- (3,4-dimethoxy-phenyl) -isoxazol-5-yl] -2-prop-2-ynyloxy-acetamide, ethyl (Z) -3- amino-2-cyano-3-phenylprop-2-enoate, picarbutrazox, pentyl N- [6 - [[(Z) - [(1-methyltetrazol-5-yl) -phenyl-methylene] amino] oxymethyl] -2- pyridyl] carbamate, 2- [2 - [(7,8-difluoro-2-methyl-3-quinolyl) oxy] -6-fluoro-phenyl] propan-2-ol, 2- [2-fluoro- 6 - [(8-fluoro-2-methyl-3-quinolyl) oxy] phenyl] propan-2-ol, 3- (5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1 -yl) quinoline, 3- (4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl) quinoline, 3- (4,4,5-trifluoro-3,3-dimethyl-3 , 4-dihydroisoquinolin-1-yl) quinoline and 9-fluoro-2,2-dimethyl-5- (3-quinolyl) -3H-1,4-benzoxazepine.

Each letter (M, B, F) of the components C listed above, as well as each combination of a letter and a number (for example, M.1 or M.1A) are considered as a group. Each pesticidal mixture comprising Bacillus amyloliquefaciens ssp. The plantarum strain MBI600 (component A) and cis-jasmone (component B) and a group of components C as defined above, is considered as an embodiment of the invention.

In one embodiment, the pesticidal mixture comprises Bacillus amyloliquefaciens ssp. plantarum strain MBI600 (component A) and cis-jasmone (component B) and at least one component C selected from the components selected from groups M, L and F.

In one embodiment, component C is selected from groups M.1 to M.29. In another embodiment, the pesticidal mixtures comprise a component C selected from groups M.1 to M.29, and a component C selected from groups F.I to F.XI. In yet another embodiment, component C is selected from groups F.1 through F.XI. In yet another embodiment, component C is selected from acetamiprid, clothianidin, cycloxaprid, dinotefuran, imidacloprid, nitenpyram, thiacloprid, and thiamethoxam. In yet another embodiment, component C is selected from ethiprole, fipronil, flufiprole, pyrafluprole, and pyriprole. In yet another embodiment, component C is selected from acrinathrin, allethrin, d-cistrans allethrin, d-trans allethrin, bifenthrin, bioalethrin, bioalethrin S-cycloclopetenyl, bioresmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha-cypermethrin, betacypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin, deltamethrin, empenthrin, sphenvalerate, etofenprox, fenpropathrin, fenvalerate, fluxytrin, fluxtrinate, half-fluiprine, methrothrine, fluxedrine, half-glutamine metofluthrin, momfluorothrin, permethrin, phenothrin, pralethrin, profluthrin, pyrethrum (pyrethrum), resmethrin, silafluofen, tefluthrin, tetramethylfluthrin, tetramethrin, tralomethrin, and transfluthrin. In still another embodiment, component C comprises at least one compound selected from azoxystrobin, cumethoxystrobin, coumoxystrobin, dimoxystrobin, enestroburin, phenaminstrobin, phenoxystrobin / fluphenoxystrobin, fluoxastrobin, cresoxim-methyl, mandestrobin, picoxystrobin, metominosxystrobin, picoxystrobin, or metominostrobin. pyraoxystrobin, trifloxystrobin, pyribencarb, triclopyricarb / chlorodincarb, famoxadone, and fenamidone.

In yet another embodiment, Component C is selected from benodanyl, benzovindiflupir, bixafen, boscalid, carboxin, fenfuram, fluopyram, flutolanil, fluxapyroxad, furametpyr, isofetamid, isopyrazam, mepronil, oxycarboxin, penflufen, pentalamiopyride, sedathoxyfluoride, and thymiopyride. In yet another embodiment, component C is selected from diflumethorim, binapacryl, dinobuton, dinocap, fluazinam, ferimzone, fenthin acetate, fenthin chloride, fenthin hydroxide, methoctradine, and silthiopham. In still another embodiment, Component C is selected from azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconabuzole, myclobconazole, paconazole, mycloporazzole. , penconazole, propiconazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole, uniconazole, imazalil, pefurazoate, prochloraz, triflumizole, fenarimol, nuarimol, pyrifenox, and triphorin. In yet another embodiment, component C is selected from aldimorph, dodemorph, dodemorph acetate, fenpropimorph, tridemorph, fenpropidine, piperaline, and spiroxamine. In yet another embodiment, component C is phenexamide. In yet another embodiment, component C is selected from benalaxyl, benalaxyl-M, kiralaxyl, metalaxyl, metalaxyl-M (mephenoxam), ofurace, and oxadixyl. In yet another embodiment, component C is selected from benomyl, carbendazim, fuberidazole, thiabendazole, and thiophanate methyl. In yet another embodiment, component C is selected from cyprodinil, mepanipyrim, and pyrimethanil. In yet another embodiment, component C is selected from fluoroimide, iprodione, procymidone, vinclozolin, fenpiclonil, and fludioxonil.

In yet another embodiment, component C is selected from ferbam, mancozeb, maneb, metam, metiram, propineb, thiram, zineb, and ziram. In yet another embodiment, component C is selected from anilazine, chlorothalonil, captafol, captan, folpet, dichlorofluanide, dichlorophene, hexachlorobenzene, pentachlorophenol and its salts, and phthalide. In yet another embodiment, component C comprises is selected from pyroquilon, tricyclazole, carpropamid, dicyclomet, and phenoxanil. In yet another embodiment, component C is selected from thiamethoxam, imidacloprid, clothianidin, metalaxyl, pyraclostrobin, fluxapyroxad, prothioconazole, penflufen, trifloxstrobin, sedaxane, azoxystrobin, abamectin, and azoxystrobin. In yet another embodiment, component C is selected from clothianidin, thiamethoxam, acetamiprid, imidacloprid, tefluthrin, bifenthrin, fipronil, thiodicarb, ciazipir, rinaxapir; and / or sedaxane, penflufen, fluopyram, fluxypyroxad, azoxystrobin, trifloxystrobin, pyraclostrobin, oxathiapyroline, metalaxyl, metalaxyl-M, ethaboxam, dimethomorph, prothioconazole, thiabendazole, ipconazole, trithudioanyl methylate, and thiofudioanyl methio-nazole.

In one embodiment, component C is selected from the group consisting of carbofuran, oxamyl, thiodicarb, fipronil, bifenthrin, cyfluthrin, beta-cyfluthrin, alpha-cypermethrin, tefluthrin, acetamipride, clothianidin, imidaclopride, thiaclopride, thiamethoxam, proteins Bt culture: Cry1Ab, Cry1Ac, Cry1Fa, Cry2Ab, mCry3A, Cry3Ab, Cry3Bb, Cry34 / 35Ab1, chlorantraniliprole, cyantraniliprole, tetraniliprol, broflanilida fluopyram, sulfoxaflor, tioxazafen, triflumezopirim, Bacillus firmus, Pasteuria spp, P. nishizawae, P.. penetrans, Rhizobium leguminosarum bv. phaseoli, R. l. bv. trifolii, R. l. bv. viciae, R. tropici, azoxystrobin, pyraclostrobin, trifloxystrobin, fluopyram, fluxapyroxad, penflufene, sedaxane, fluazinam, difenoconazole, ipconazole, prothioconazole, tebuconazole, triticonazole, metalaxyl, metalaxypyramine, and oxapyroxyl-M.

In one embodiment, component C is selected from the group consisting of cyclaniliprole, carbofuran, oxamyl, thiodicarb, fipronil, bifenthrin, cyfluthrin, beta-cyfluthrin, alpha-cypermethrin, tefluthrin, acetamiprid, clothianidin, imidacloprid, thiametoxamid, thiameclopridam, chlorantraniliprole, cyantraniliprole, tetranyliprole, broflanilide, sulfoxaflor, thioxazafen, triflumezopyrim, and the Bacillus thuringiensis proteins Cry1Ab, Cry1Ac, Cry1Fa, Cry2Ab, mCry3A, Cry3Ab, Cry3Bb, and Cry34 / 351.

In one embodiment, component C is selected from the group consisting of Bacillus firmus, Pasteuria nishizawae, Pasteuria penetrans, Rhizobium leguminosarum bv. phaseoli, Rhizobium leguminosarum bv. trifolii, Rhizobium leguminosarum bv. viciae, Burkholderia spp. and Rhizobium tropici.

In one embodiment, component C is selected from the group consisting of azoxystrobin, pyraclostrobin, trifloxystrobin, fluopyram, fluxapyroxad, penflufene, sedaxane, fluazinam, difenoconazole, ipconazole, prothioconazole, tebuconazole, triticonazole, metalaxyl-mconazole (meconazole-Mconazole) (meconazole-Mconazole) , thiabendazole, fludioxonil, benzovindiflupir, picarbutrazox, etaboxam, pidiflumetofen, fenpicoxamide, thiophanate methyl, myclobutanil, and oxathiapiproline.

In one embodiment, component C is selected from the group M.1A. In one embodiment, component C is selected from the group M.2B. In one embodiment, component C is selected from the group M.3A. In one embodiment, component C is selected from the group M.4A. In one embodiment, component C is selected from group M.6. In one embodiment, component C is selected from the group M.11. In one embodiment, component C is selected from the group M.28. In one embodiment, component C is selected from the group M.29.

In one embodiment, component C is selected from group L.3. In one embodiment, component C is selected from the group L. 5.

In one embodiment, component C is selected from the group F.O1. In one embodiment, component C is selected from the group F.I3. In one embodiment, component C is selected from the group F.I4. In one embodiment, component C is selected from group F.II1. In one embodiment, component C is selected from group F.III1. In one embodiment, component C is selected from group F.IV1. In one embodiment, component C is selected from group F.VI1. In one embodiment, component C is selected from group F.VII5.

The terms "component" and "compound" are interchangeable.

In one embodiment, the pesticidal mixtures comprise a pesticidal mixture I-1 to I-8 and a component C selected from Table B.

Components C in Table B are called components N-1 to N-42 and O-1 to O-42. In one embodiment, components C in Table B are called components N-1 to N-29 and O-1 to O-36 according to the corresponding row in Table B. In another embodiment, components C in Table B are called components N-30 to N-42 and O-37 to O-42 according to the corresponding row in Table B.

In another embodiment, the pesticidal mixtures comprise pesticidal mixture I-1 and a component C selected from Table B. In yet another embodiment, the pesticidal mixtures comprise pesticidal mixture I-2 and a component C selected from Table B. In In another embodiment, the pesticidal mixtures comprise the pesticidal mixture I-3 and a component C selected from Table B. In yet another embodiment, the pesticidal mixtures comprise the pesticidal mixture I-4 and a component C selected from Table B. In another Still another embodiment, the pesticidal mixtures comprise the pesticidal mixture I-5 and a component C selected from Table B. In yet another embodiment, the pesticidal mixtures comprise the pesticidal mixture I-6 and a component C selected from Table B. In another Still another embodiment, the pesticidal mixtures comprise pesticidal mixture I-7 and a component C selected from Table B. In yet another embodiment, the pesticidal mixtures comprise pesticidal mixture I-8 and a component C selected from Table B.

In one embodiment, the pesticidal mixtures comprise, as active components, Bacillus amyloliquefaciens ssp. plantarum strain MBI600 (component A) and cis-jasmone (component B) in synergistically effective amounts and a component C selected from Table B.

In one embodiment, the mixtures are applied as set forth in Table T comprising pesticidal mixture I-5 as defined in Table A which comprises as active components, Bacillus amyloliquefaciens ssp. plantarum strain MBI600 (component A) and cis-jasmone (component B) in synergistically effective amounts and also a component C selected from Table B.

In one embodiment, the mixtures are applied as set forth in Table T consisting of Bacillus amyloliquefaciens ssp. plantarum strain MBI600 (component A) and cis-jasmone (component B) in synergistically effective amounts and also a component C selected from Table B.

In one embodiment, the blends in Table T comprise an additional component C as set forth in Table B. In one embodiment, the blends in Table T comprise two additional components C as set forth set forth in Table B. In one embodiment, the mixtures of Table T comprise at least three other C components as set out in Table B.

In one embodiment, the invention relates to mixtures as set out in Tables Q comprising the pesticidal mixture I-5 as defined in Table A comprising as active components, Bacillus amyloliquefaciens ssp. plantarum strain MBI600 (component A) and cis-jasmone (component B) in synergistically effective amounts and also two components C selected from Table B.

In one embodiment, the invention relates to mixtures as set forth in Tables Q consisting of Bacillus amyloliquefaciens ssp. plantarum strain MBI600 (component A) and cis-jasmone (component B) in synergistically effective amounts and also two components C selected from Table B.

In one embodiment, these mixtures as defined in Tables Q-1 to Q-168 comprise a specific mixture as defined in Table T and another component C selected from the components defined in Table B.

In one embodiment, these mixtures as defined in Tables Q-1 to Q-168 consist of a specific mixture as defined in Table T and an additional component C selected from the components defined in Table B.

Tables Q:

In one embodiment, the pesticidal mixtures comprise at least two C components.

In one embodiment, the pesticidal mixtures comprise at least two C-components selected from the group consisting of thiamethoxam, ciazipir, rinaxypyr, fludioxonil, metalaxyl-M (mephenoxam), mephentrifluconazole, azoxystrobin, pyraclostrobin, fluxapyroxad, thiaconazole, penfluconazole, clotioxad, thiaconazole, penfluconazole, clotioxad. metalaxyl and imidaclopride.

In one embodiment, the pesticidal mixture comprises Bacillus amyloliquefaciens ssp. plantarum strain MBI600 and cisjasmone in synergistically effective amounts where the proportion of Bacillus amyloliquefaciens ssp. the plantarum strain MBI600 a cis-jasmone is 1016 CFU: 1 g to 105 CFU: 1 g. as well as fludioxonil, mefenoxam, azoxystrobin, thiabendazole, and clothianidin.

In one embodiment, the pesticidal mixture comprises Bacillus amyloliquefaciens ssp. Plantarum strain MBI600 and amounts of cis-jasmone where the proportion of Bacillus amyloliquefaciens ssp. the plantarum strain MBI600 a cis-jasmone is 1016 CFU: 1 g to 105 CFU: 1 g. in addition to prothioconazole, penflufen, metalaxyl, and imidaclopride. In one embodiment, the pesticidal mixture comprises Bacillus amyloliquefaciens ssp. Plantarum strain MBI600 and amounts of cis-jasmone where the proportion of Bacillus amyloliquefaciens ssp. the plantarum strain MBI600 a cis-jasmone is 1016 CFU: 1 g to 105 CFU: 1 g. as well as pyraclostrobin, fluxapyroxad, metalaxyl, and imidaclopride. In one embodiment, the pesticidal mixtures comprise at least one component C selected from groups M.1 to M.29, and at least one component C selected from groups FI to F.XI. In one embodiment, the pesticidal mixtures comprise at least one component C selected from groups M.1 to M.29, and at least one component C selected from groups L.1 to L.5. In one embodiment, the pesticidal mixtures comprise at least one component C selected from groups FI to F.XI, and at least one component C selected from groups L.1 to L.5.

The invention also relates to agrochemical compositions comprising an auxiliary and pesticidal mixtures. In one embodiment, the agrochemical composition comprises more than one auxiliary and the pesticidal mixture. In one embodiment, the invention relates to a seed treatment composition comprising the pesticide mixtures and at least one auxiliary, wherein the auxiliary is preferably selected from surfactants, antifreeze agents, binders and pigments, and in particular a surfactant or a binder. The types of formulation of the seed treatment composition are given below.

Pesticidal mixtures comprise a pesticidal effective amount of Bacillus amyloliquefaciens, cis-jasmone, and optionally component C. The term "pesticidal effective amount" is defined below.

The pesticide mixtures can be converted into common types of agrochemical compositions, eg, solutions, emulsions, suspensions, powders, sprays, pastes, granules, presses, capsules, and mixtures thereof. Examples of types of agrochemical composition are suspensions (eg SC, OD, FS), emulsifiable concentrates (eg EC), emulsions (eg ^e W, EO, ES, ME), capsules (eg CS, ZC), pastes, tablets, wettable powders or powders (eg WP, SP, WS, DP, DS), pressed (eg BR, TB, DT), granules (eg WG, SG, GR, FG , GG, MG), insecticidal articles (eg LN), as well as gel formulations for the treatment of plant propagation materials such as seeds (eg GF). These and other types of agrochemical compositions are defined in the "Catalog of pesticide formulation types and international coding system", Technical Mono-graph No. 2, 6th Ed. May 2008, CropLife International.

Agrochemical compositions are prepared in a 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 Informs, London, 2005.

Examples of suitable auxiliaries are solvents, liquid vehicles, solid vehicles or fillers, surfactants, dispersants, emulsifiers, humectants, adjuvants, solubilizers, penetration enhancers, protective colloids, adhesion agents, thickeners, humectants, repellants, attractants, feed stimulants, compatibilizers, bactericides, antifreeze agents, antifoam agents, colorants, adhesives and binders.

Suitable liquid solvents and vehicles are water and organic solvents, such as medium to high boiling 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, for example cyclohexanone; esters, for example lactates, carbonates, fatty acid esters, gamma-butyrolactone; fatty acids; phosphonates; amines; amides, eg, N-methylpyrrolidone, fatty acid dimethylamides; and mixtures thereof.

Suitable solid carriers or fillers are mineral earths, for example silicates, silica gels, talc, kaolin, limestone, lime, chalk, clays, dolomite, diatomaceous earth, bentonite, calcium sulfate, magnesium sulfate, magnesium; powdered polysaccharides, eg cellulose, starch; fertilizers, for example ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas; products of plant origin, for example, cereal flour, tree bark flour, wood flour, walnut shell flour and mixtures thereof.

Suitable surfactants are surfactant compounds, such as anionic, cationic, nonionic, and amphoteric surfactants, block polymers, polyelectrolytes, and mixtures thereof. Said surfactants can be used as emulsifiers, dispersants, solubilizers, humectants, penetration enhancers, protective colloids or adjuvants. Examples of surfactants are listed in McCutcheon, Vol.1: Emulsifiers & Detergents, McCutcheon Directories, Glen Rock, USA, 2008 (International Ed. Or North American Ed.).

Suitable anionic surfactants are alkali, alkaline earth or ammonium salts of sulfonates, sulfates, phosphates, carboxylates, and mixtures thereof. Examples of sulfonates are alkylaryl sulfonates, diphenylsulfonates, alpha-olefin sulfonates, lignin sulfonates, fatty acid and oil sulfonates, ethoxylated alkylphenol sulfonates, alkoxylated arylphenol sulfonates, condensed naphthalene sulfonates, dodecyl sulfonates, and alkyl tridelene benzene sulfonates , 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 carboxylated alcohol or alkylphenol ethoxylates.

Suitable nonionic surfactants are alkoxylates, N-substituted fatty acid amides, amine oxides, esters, sugar-based surfactants, polymeric surfactants, and mixtures thereof. Examples of alkoxylates are compounds such as alcohols, alkylphenols, amines, amides, arylphenols, fatty acids, or fatty acid esters that have been alkoxylated with 1 to 50 equivalents. Ethylene oxide and / or propylene oxide can be used for the alkoxylation, preferably ethylene oxide. Examples of N-substituted fatty acid amides 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 sorbitan, Ethoxylated sorbitans, sucrose-glucose esters or alkylpolyglycosides. Examples of polymeric surfactants are homo- or copolymers of vinylpyrrolidone, vinyl alcohols, or vinyl acetate.

Suitable cationic surfactants are quaternary surfactants, for example quaternary ammonium compounds with one or two hydrophobic groups, or long chain primary amine salts. Suitable amphoteric surfactants are alkyl betaines and imidazolines. Suitable block polymers are block polymers of the N-B or N-O-A type comprising blocks of polyethylene oxide and polypropylene oxide, or of the N-O-C type comprising alkanol, polyethylene oxide and polypropylene oxide. Suitable polyelectrolytes are polyacids or polybases. Examples of polyacids are alkali salts of polyacrylic acid or comb polymers of polyacids. Examples of polybases are polyvinylamines or polyethyleneamines.

Suitable adjuvants are compounds, which have negligible or even no pesticidal activity, and which improve the biological performance of the compounds of the present invention in 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 Informa UK, 2006, Chapter 5.

Suitable thickeners are polysaccharides (eg, xanthan gum, carboxymethylcellulose), anorganic clays (organically modified or unmodified), polycarboxylates, and silicates.

Suitable bactericides are bronopol and isothiazolinone derivatives such as alkyl isothiazolinones and benzisothiazolinones.

Suitable antifreeze agents are ethylene glycol, propylene glycol, urea, and glycerin.

Suitable antifoaming agents are silicones, long chain alcohols, and fatty acid salts. Suitable colorants (eg red, blue or green) are low water solubility pigments and water soluble colorants. Examples are inorganic dyes (eg, iron oxide, titanium oxide, iron hexacyanoferrate) and organic dyes (eg, alizarin, azo, and phthalocyanine dyes).

Suitable binders or binders are polyvinylpyrrolidones, polyvinyl acetate, polyvinyl alcohols, polyacrylates, biological or synthetic waxes, and cellulose ethers.

Examples of types of agrochemical composition and their preparation are:

i) Water soluble concentrates (SL, LS)

10-60% by weight of the pesticide mixtures according to the invention and 5-15% by weight of wetting agent (for example alcohol alkoxylates) are dissolved in water and / or in a water soluble solvent (for example , alcohols) up to 100% by weight. The active ingredient dissolves after dilution with water.

ii) Dispersible concentrates (CD)

5-25% by weight of the pesticidal mixtures according to the invention and 1-10% by weight of dispersant (eg polyvinylpyrrolidone) are dissolved in up to 100% by weight of organic solvent (eg cyclohexanone). Dilution with water gives a dispersion.

iii) Emulsifiable concentrates (CE)

15-70% by weight of the pesticide mixtures according to the invention and 5-10% by weight of emulsifiers (for example, calcium dodecylbenzenesulfonate and castor oil ethoxylate) dissolve in up to 100% by weight of water insoluble organic solvent (eg aromatic hydrocarbon). Dilution with water gives an emulsion.

iv) Emulsions (EW, EO, ES)

5-40% by weight of the pesticide mixtures according to the invention and 1-10% by weight of emulsifiers (for example, calcium dodecylbenzenesulfonate and castor oil ethoxylate) are dissolved in 20-40% by weight of solvent water insoluble organic (eg aromatic hydrocarbon). This mixture is introduced into up to 100% by weight of water by means of an emulsifying machine and becomes a homogeneous emulsion. Dilution with water gives an emulsion.

v) Suspensions (SC, OD, FS)

In a stirred ball mill, 20-60% by weight of the pesticide mixtures according to the invention are ground with the addition of 2-10% by weight of dispersants and wetting agents (for example sodium lignosulfonate and ethoxylate of alcohol), 0.1-2% by weight of thickener (eg xanthan gum) and up to 100% by weight of water to give a fine suspension of active substance. Dilution with water provides a stable suspension of the active substance. For the FS type composition, up to 40% by weight of binder (eg polyvinyl alcohol) is added.

vi) Water dispersible granules and water soluble granules (WG, SG)

50-80% by weight of the pesticidal mixtures according to the invention are finely ground with the addition of up to 100% by weight of dispersants and wetting agents (eg sodium lignosulfonate and alcohol ethoxylate) and prepared as dispersible granules in water or soluble in water by means of technical apparatus (eg extrusion, spray tower, fluidized bed). Dilution with water provides a stable dispersion or solution of the active substance.

vii) Water dispersible powders and water soluble powders (WP, SP, WS)

50-80% by weight of the pesticide mixtures according to the invention are ground in a rotor-stator mill with the addition of 1-5% by weight of dispersants (for example sodium lignosulfonate), 1-3% by weight of wetting agents (eg alcohol ethoxylate) and up to 100% by weight of solid carrier, eg silica gel Dilution with water provides a stable dispersion or solution of the active substance.

viii) Gel (GW, GF)

In a stirred ball mill, 5-25% by weight of the pesticide mixtures according to the invention are ground with the addition of 3-10% by weight of dispersants (for example sodium lignosulfonate), 1-5% by weight of thickener (eg carboxymethyl cellulose) and more than 100% by weight of water to give a fine suspension of the active substance. Dilution with water provides a stable suspension of the active substance.

ix) Microemulsion (ME)

5-20% by weight of the pesticide mixtures according to the invention are added to 5-30% by weight of organic solvent mixture (for example, fatty acid dimethylamide and cyclohexanone), 10-25% by weight of mixture of surfactant (eg, alcohol ethoxylate and arylphenol ethoxylate), and water up to 100%. This mixture is stirred for 1 h to spontaneously produce a thermodynamically stable microemulsion.

x) Microcapsules (CS)

An oil phase comprising 5-50% by weight of the pesticidal mixtures according to the invention, 0-40% by weight of water-insoluble organic solvent (for example aromatic hydrocarbon), 2-15% by weight of acrylic monomers (eg, methyl methacrylate, methacrylic acid, and a di- or triacrylate) are dispersed in an aqueous solution of a protective colloid (eg, polyvinyl alcohol). Radical polymerization initiated by a radical initiator results in the formation of poly (meth) acrylate microcapsules. Alternatively, an oil phase comprising 5-50% by weight of a compound I according to the invention, 0-40% by weight of water-insoluble organic solvent (for example aromatic hydrocarbon) and an isocyanate monomer (for example , diphenylmethene-4,4'-diisocyanates) are dispersed in an aqueous solution of a protective colloid (eg, polyvinyl alcohol). The addition of a polyamine (eg, hexamethylenediamine) results in the formation of a polyurea microcapsule. The monomers amount to 1-10% by weight. The% by weight refers to the total composition of CS.

xi) Adjustable powders (DP, DS)

1-10% by weight of the pesticide mixtures according to the invention are finely ground and intimately mixed with up to 100% by weight of solid carrier, for example finely divided kaolin.

xii) Granules (GR, FG)

0.5-30% by weight of the pesticide mixtures according to the invention are finely ground and associated with up to 100% by weight of solid carrier (eg silicate). Granulation is achieved by extrusion, spray drying or fluidized bed.

xiii) Ultra Low Volume Liquids (UL)

1-50% by weight of the pesticide mixtures according to the invention are dissolved in up to 100% by weight of organic solvent, for example aromatic hydrocarbon

The agrochemical compositions of types i) to xi) can optionally comprise other auxiliaries, such as 0.1-1% by weight of bactericides, 5-15% by weight of antifreeze agents, 0.1-1% by weight of antifoam agents and 0.1- 1% by weight colorants.

Agrochemical compositions generally comprise between 0.01 and 95%, preferably between 0.1 and 90%, and most preferably between 0.5 and 75%, by weight of active pesticidal substances. The pesticidally active substrate is used in a purity of 90% to 100%, preferably 95% to 100% (according to the NMR spectrum).

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 the compositions that compose them as a premix or, if applicable, until immediately prior to use (tank mix). These agents can be mixed with the compositions according to the invention in a weight ratio of 1: 100 to 100: 1, preferably 1:10 to 10: 1.

The user applies the mixture according to the invention generally from a pre-dosing device, a backpack sprayer, a spray tank, a spray plane or an irrigation system. Usually, the agrochemical composition is composed of water, regulator and / or additional auxiliaries for the desired application concentration and thus the ready-to-use spray liquor or the agrochemical composition according to the invention is obtained. Generally, 20 to 2000 liters, preferably 50 to 400 liters, of the ready-to-use spray liquor are applied per hectare of useful agricultural area.

According to one embodiment, the individual components of the pesticidal mixture according to the invention, such as parts of a binary or ternary mixture, can be mixed by the user himself in a spray tank and additional auxiliaries can be added, if appropriate. .

In a further embodiment, individual components of the pesticidal mixtures according to the invention or partially premixed components, for example Bacillus amyloliquefaciens, cis-jasmone and optionally component C can be mixed by the user in a spray tank and can be added more auxiliaries and additives, if applicable.

In a further embodiment, the individual components of the mixture according to the invention, or the partially premixed components, i.e. Bacillus amyloliquefaciens, or cis-jasmone, and optionally component C, can be applied together (e.g. after mixing mixing in the tank) or consecutively in the application. methods of the invention. In one embodiment, the individual components or partially premixed components, i.e., Bacillus amyloliquefaciens or cis-jasmone, and optionally Component C, are applied to the plant propagation material prior to planting, followed by soil treatment or treatment. foliar with the other component (s) of the pesticide mixtures after planting. The period between seed treatment of plant propagation material before sowing and treatment after sowing generally varies with the period of vegetation, the plant, irrigation techniques, pests, soil, humidity and the weather. Usually the period ranges from 1 day to 3 months, preferably 10 days to 1 month.

The pesticidal mixture is suitable for controlling pests, such as arthropods, mites, nematodes and fungi. Therefore, the pesticide mixtures can be applied in a method to control the unwanted attack of insects, nematodes or mites, harmful fungi, wherein the pesticide mixtures can act on the respective pests, their environment or the crop plants to protect from respective pest, in the soil, and / or in the crop plants, and / or in their environment.

The compounds of the present invention are suitable for use in protecting crops, plants, plant propagation materials, such as seeds or soil or water, in which the plants are growing, from attack or infestation by animal pests.

Therefore, the invention also relates to a method of controlling pests, which method comprises applying a mixture of pesticides to plants, plant propagation material or the place of growth of plants; pests or their food supply, habitat or breeding grounds, excluding methods for treating the human or animal body by surgery or therapy. It is also related to the use of pesticide mixtures to control and prevent pests, for example, on plants, plant parts in the soil, and on plant propagation material. The term controlling both refers to the treatment of infested plants, parts of them, plant propagation material and the soil, but also to the prevention of infestation before the respective pests are present. In one embodiment, the pesticidal mixture is applied to the plant propagation material. In one embodiment, the invention relates to methods of controlling pests while applying mixtures comprising Bacillus amyloliquefaciens ssp. plantarum strain MBI600 (component A) and cis-jasmone (component B) in synergistically effective amounts where the proportion of Bacillus amyloliquefaciens ssp. the plantarum strain MBI600 a cis-jasmone is 1016 CFU: 1 g to 105 CFU: 1 g.

In another embodiment, the invention relates to methods of controlling pests while mixtures comprising Bacillus amyloliquefaciens ssp. plantarum strain MBI600 (component A) and cis-jasmone (component B) in synergistically effective amounts where the proportion of Bacillus amyloliquefaciens ssp. the plantarum strain MBI600 a cis-jasmone is 1016 CFU: 1 g to 105 CFU: 1 g. and at least one other additional component C is applied.

Pesticide mixtures are suitable for efficiently controlling animal pests such as arthropods, gastropods, and nematodes, including but not limited to:

insects of the order Lepidoptera, for example Achroia grisella, Acleris spp. as A. fimbriana, A. gloverana, A. variana; Acrolepiopsis assectella, Acronicta major, Adoxophyes spp. as A. cyrtosema, A. orana; Aedia leucomelas, Agrotis spp. as A. exclamationis, A. fucosa, A. Ípsilon, A. orthogoma, A. segetum, A. subterranea; Alabama argillacea, Aleurodicus dispersus, Alsophila pometaria, Ampelophaga rubiginosa, Amyelois transitella, Anacampsis sarcitella, Anagasta kuehniella, Anarsia lineatella, Anisota senatoria, Antheraea pernyi, Anticarsia ( = Thermesia) spp. as A. gemmatalis; Apamea spp., Aproaerema modicella, Archips spp. as A. argyrospila, A. fuscocupreanus, A. rosana, A. xyloseanus; Argyresthia conjugella, Argyroploce spp., Argyrotaenia spp. as A. velutinana; Athetis mindara, Austroasca viridigrisea, Autographa gamma, Autographa nigrisigna, Barathra brassicae, Bedellia spp., Bonagota salubricola, Borbo cinnara, Bucculatrix thurberiella, Bupalus piniarius, Busseola spp., Cacoecia spp. as C. murinana, C. podana; Cactoblastis cactorum, Cadra cautella, Calingo brazliensis, Caloptilis theivora, Capua reticulana, Carposina spp. as C. niponensis, C. sasakii; Cephus spp., Chaetocnema aridula, Cheimatobia brumata, Chilo spp. as C. Indicus, C. suppressalis, C. partellus; Choreutis pariana, Choristoneura spp. as C. conflictana, C. fumiferana, C. longicellana, C. murinana, C. occidentalis, C. rosaceana; Chrysodeixis ( = Pseudoplusia) spp. as C. eriosoma, C. includens; Cirphis unipuncta, Clysia ambiguella, Cnaphalocerus spp., Cnaphalocrocis medinalis, Cnephasia spp., Cochylis hospes, Coleophora spp., Colias eurytheme, Conopomorpha spp., Conotrachelus spp., Copitarsia spp. , Corcytermbus cembus calla lspp., Corcytermbus cembus calla lspp. = Epinotia) aporema, Cydalima ( = Diaphania) perspectalis, Cydia ( = Carpocapsa) spp. as C. pomonella, C. latiferreana; Dalaca noctuides, Datana integerrima, Dasychira pinicola, Dendrolimus spp. as D. pini, D. spectabilis, D. sibiricus; Desmia funeralis, Diaphania spp. as D. nitidalis, D. hyalinata; Diatraea grandiosella, Diatraea saccharalis, Diphthera festiva, Earias spp. such as E. insulana, E. vittella; Ecdytolopha aurantianu, Egira ( = Xylomyges) curialis, Elasmopalpus lignosellus, Eldana saccharina, Endopiza viteana, Ennomos subsignaria, Eoreuma loftini, Ephestia spp. such as E. cautella, E. elutella, E. kuehniella; Epinotia aporema, Epiphyas postvittana, Erannis tiliaria, Erionota thrax, Etiella spp., Eulia spp., Eupoecilia ambiguella, Euproctis chrysorrhoea, Euxoa spp., Evetria bouliana, Faronta albilinea, Feltia spp. as F. subterranean; Galleria mellonella, Gracillaria spp., Grapholita spp. as G. funebrana, G. molesta, G. inopinata; Halysidota spp., Harrisina americana, Hedylepta spp., Helicoverpa spp. as H. armigera ( = Heliothis armigera), H. zea ( = Heliothis zea); Heliothis spp. such as H. assulta, H. subflexa, H. virescens; Hellula spp. as H. undalis, H. rogatalis; Helocoverpa gelotopoeon, Hemileuca oliviae, Herpetogramma licarsisalis, Hibernia defoliaria, Kephmannophila pseudospretella, Homoeosoma electellum, Homona magnanima, Hypena scabra, Hyphantria cunea, Hyponomeuta padella, Hyponomeuta kapivlinellusina indica, Lambcellaria lymphophila pseudospretella indication Laspeyresia molesta, Leguminivora glycinivorella, Lerodea eufala, Leucinodes orbonalis, Leucoma salicis, Leucoptera spp. as L. coffeella, L. scitella; Leuminivora lycinivorella, Lithocolletis blancardella, Lithophane antennata, Llattia octo ( = Amyna axis), Lobesia botrana, Lophocampa spp., Loxagrotis albicosta, Loxostege spp. as L. sticticalis, L. cereralis; Lymantria spp. as L. dispar, L. monacha; Lyonetia clerkella, Lyonetia prunifoliella, Malacosoma spp. as M. americanum, M. californicum, M. constrictum, M. neustria; Mamestra spp. such as M. brassicae, M. configurata; Mamstra brassicae, Manduca spp. as M. quinquemaculata, M. sexta; Marasmia spp, Marmara spp., Maruca testulalis, Megalopyge lanata, Melanchra picta, Melanitis leda, Mocis spp. as M. lapites, M. repanda; Latipes Mods, Monochroa fragariae, Mythimna separata, Nemapogon cloacella, Neoleucinodes elegantalis, Nepytia spp., Nymphula spp., Oiketicus spp., Omiodes indicata, Omphisa anastomosalis, Operophtera brumata, Orgyia pseudotsugata, Oria spp., Orthaga thyrisalis, Ostrinia spp. as O. nubilalis; Oulema oryzae, Paleacrita vernata, Panolis flammea, Parnara spp., Papaipema nebris, Papilio cresphontes, Paramyelois transitella, Paranthrene regalis, Paysandisia archon, Pectinophora spp. as P. gossypiella; Peridroma saucia, Perileucoptera spp., Like P. coffeella; Phalera bucephala, Phryganidia californica, Phthorimaea spp. as P. operculella; Phyllocnistis citrella, Phyllonorycter spp. such as P. blancardella, P. crataegella, P. issikii, P. ringoniella; Pieris spp. such as P. brassicae, P. rapae, P. napi; Pilocrocis tripunctata, Plathypena scabra, Platynota spp. as P. flavedana, P. idaeusalis, P. stultana; Platyptilia carduidactyla, Plebejus argus, Plodia interpunctella, Plusia spp, Plutella maculipennis, Plutella xylostella, Pontia protodica, Prays spp., Prodenia spp., Proxenus lepigone, Pseudaletia spp. such as P. sequax, P. unipuncta; Pyrausta nubilalis, Rachiplusia nu, Richia albicosta, Rhizobius ventralis, Rhyacionia frustrana, Sabulodes aegrotata, Schizura concinna, Schoenobius spp., Schreckensteinia festaliella, Scirpophaga spp. as S. incertulas, S. innotata; Scotia segetum, Sesamia spp. such as S. inferens, Seudyra subflava, Sitotroga cerealella, Sparganothis pilleriana, Spilonota lechriaspis, S. ocellana, Spodoptera ( = Lamphygma) spp. such as S. cosmoides, S. eridania, S. exigua, S. frugiperda, S. latisfascia, S. littoralis, S. litura, S. omithogalli; Stigmella spp., Stomopteryx subsecivella, Strymon bazochii, Sylepta derogata, Synanthedon spp. such as S. exitiosa, Tecia solanivora, Telehin licus, Thaumatopoea pityocampa, Thaumatotibia ( = Cryptophlebia) leucotreta, Thaumetopoea pityocampa, Thecla spp., Theresimima ampelophaga, Thyrinteina spp, Tildenia inconspicuella, Tinea spp. as T. cloacella, T. pellionella; Tineola bisselliella, Tortrixspp. as T. viridana; Trichophaga tapetzella, Trichoplusia spp. as T. ni; Tuta ( = Scrobipalpula) absolutes, Udea spp. as U. rubigalis, U. rubigalis; Virachola spp., Yponomeuta padella, and Zeiraphera canadensis;

insects of the order Coleoptera, for example Acalymma vittatum, Acanthoscehdes obtectus, Adoretus spp., Agelastica alni, Agrilus spp. as A. anxius, A. planipennis, A. sinuatus; Agriotes spp. as A. fuscicollis, A. lineatus, A. obscurus; Alphitobius diaperinus, Amphimallus solstitialis, Anisandrus dispar, Anisoplia austriaca, Anobium punctatum, Anomala corpulenta, Anomala rufocuprea, Anoplophora spp. as A. glabripennis; Anthonomus spp. as A. eugenii, A. grandis, A. pomorum; Anthrenus spp., Aphthona euphoridae, Apion spp., Apogonia spp., Athous haemorrhoidalis, Atomaria spp. as A. linearis; Attagenus spp., Aulacophora femoralis, Blastophagus piniperda, Blitophaga undata, Bruchidius obtectus, Bruchus spp. as B. lentis, B. pisorum, B. rufimanus; Byctiscus betulae, Callidiellum rufipenne, Callopistria floridensis, Callosobruchus chinensis, Cameraria ohridella, Cassida nebulosa, Cerotoma trifurcata, Cetonia aurata, Ceuthorhynchus spp. as C. assimilis, C. napi; Chaetocnema tibialis, Cleonus mendicus, Conoderus spp. as C. vespertinus; Conotrachelus nenuphar, Cosmopolites spp., Costelytra zealandica, Crioceris asparagi, Cryptolestes ferrugineus, Cryptorhynchus lapathi, Ctenicera spp. as C. destructor; Curculio spp., Cylindrocopturus spp., Cyclocephala spp., Dactylispa balyi, Dectes texanus, Dermestes spp., Diabrotica spp. as D. undecimpunctata, D. speciosa, D. longicornis, D. semipunctata, D. virgifera; Diaprepes abbreviates, Saidcrocis spp., Dicladispa armigera, Diloboderus abderus, Diocalandra frumenti ( Diocalandra stigmaticollis), Enaphalodes rufulus, Epilachna spp. as E. varivestis, E. vigintioctomaculata; Epitrixspp. such as E. hirtipennis, E. similaris; Eutheola humilis, Eutinobothrus brasiliensis, Faustinus cubae, Gibbium psylloides, Gnathocerus cornutus, Hellula undalis, Heteronychus arator, Hylamorpha elegans, Hylobius abietis, Hylotrupes bajulus, Hypera spp. as H. brunneipennis, H. postica; Hypomeces squamosus, Hypothenemus spp., Lps typographus, Lachnosterna consanguinea, Lasioderma serricorne, Latheticus oryzae, Lathridius spp., Lema spp. as L. bilineata, L. melanopus; Leptinotarsa spp. as L. decemlineata; Leptispa pygmaea, Limonius californicus, Lissorhoptrus oryzophilus, Lixus spp., Luperodes spp., Lyctus spp. as L. bruneus; Liogenys fuscus, Macrodactylus spp. as M. subspinosus; Matryoshka, Megaplatypus mutates, Megascelis spp., Melanotus communis, Meligethes spp. as M. aeneus; Melolontha spp. such as M. hippocastani, M. melolontha; Metamasius hemipterus, Microtheca spp., Migdolus spp. such as M. fryanus, Monochamus spp. as M. alternates; Naupactus xanthographus, Niptus hololeucus, Oberia brevis, Oemona hirta, Oryctes rhinoceros, Oryzaephilus surinamensis, Oryzaphagus oryzae, Otiorrhynchus sulcatus, Otiorrhynchus ovatus, Otiorrhynchus sulcatus, Oulema melanozapus . as P. brassicae, P. cochleariae; Phoracantha recurva, Phyllobius pyri, Phyllopertha horticola, Phyllophaga spp. as P. helleri; Phyllotreta spp. such as P. chrysocephala, P. nemorum, P. striolata, P. vittula; Phyllopertha horticola, Popillia japonica, Premnotrypes spp., Psacothea hilaris, Psylliodes chrysocephala, Prostephanus truncates, Psylliodes spp., Ptinus spp. , Hog flea, Rhizopertha dominica, Rhynchophorus spp. such as R. billineatus, R. ferrugineus, R. palmarum, R. phoenicis, R. vioratus; Saperda candida, Scolytus schevyrewi, Scyphophorus acupunctatus, Sitona lineatus, Sitophilus spp. such as S. granaria, S. oryzae, S. zeamais; Sphenophorus spp. like S. levis; Stegobium paniceum, Sternechus spp. as S. subsignatus; Strophomorphus ctenotus, Symphyletes spp., Tanymecus spp., Tenebrio molitor, Tenebrioides mauretanicus, Tribolium spp. as T. castaneum; Trogoderma spp., Tychius spp., Xylotrechus spp. as X. pyrrhoderus; and, Zabrus spp. as Z. tenebrioides;

insects of the order Diptera, for example Aedes spp. as A. aegypti, A. albopictus, A. vexans; Anastrepha ludens, Anopheles spp. such as A. albimanus, A. crucians, A. freeborni, A. gambiae, A. leucosphyrus, A. maculipennis, A. minimus, A. quadrimaculatus, A. sinensis; Bactrocera invadens, Bibio hortulanus, Calliphora erythrocephala, Calliphora vicina, Ceratitis capitata, Chrysomyia spp. as C. bezziana, C. hominivorax, C. macellaria; Chrysops atlanticus, Chrysops discalis, Chrysops silacea, Cochliomyia spp. as C. hominivorax; Contarinia spp. as C. sorghicola; Cordylobia anthropophaga, Culex spp. as C. nigripalpus, C. pipiens, C. quinquefasciatus, C. tarsalis, C. tritaeniorhynchus; Culicoides furens, Culiseta inornata, Culiseta melanura, Cuterebra spp., Dacus cucurbitae, Dacus oleae, Dasineura brassicae, Dasineura oxycoccana, Delia spp. as D. antique, D. coarctata, D. platura, D. radicum; Dermatobia hominis, Drosophila spp. such as D. suzukii, Fannia spp. as F. canicularis; Gastraphilus spp. as G. intestinalis; Geomyza tipunctata, Glossina spp. as G. fuscipes, G. morsitans, G. palpalis, G. tachinoides; Haematobia irritans, Haplodiplosis equestris, Hippelates spp., Hylemyia spp. as H. platura; Hypoderma spp. as H. lineata; Hyppobosca spp., Hydrellia philippina, Leptoconops torrens, Liriomyza spp. as L. sativae, L. trifolii; Lucilia spp. as L. caprina, L. cuprina, L. sericata; Lycoria pectoralis, Mansonia titillanus, Mayetiola spp. as M. destructor; Musca spp. as M. autumnalis, M. domestica; Muscina stabulans, Oestrus spp. as O. ovis; Opomyza florum, Oscinella spp. as O. frit; Orseolia oryzae, Pegomya hysocyami, Phlebotomus argentipes, Phorbia spp. such as P. antiqua, P. brassicae, P. coarctata; Phytomyza gymnostoma, Prosimulium mixtum, Psila rosae, Psorophora columbiae, Psorophora discolor, Rhagoletis spp. such as R. cerasi, R. cingulate, R. indifferens, R. mendax, R. pomonella; Rivellia quadrifasciata, Sarcophaga spp. as S. haemorrhoidalis; Simulium vittatum, Sitodiplosis mosellana, Stomoxys spp. as S. calcitrans; Tabanus spp. as T. atratus, T. bovinus, T. lineola, T. similis; Tannia spp., Thecodiplosisjaponensis, Tipula oleracea, Tipula paludosa, and Wohlfahrtia spp;

insects of the order Thysanoptera, for example, Baliothrips biformis, Dichromothrips corbetti, Dichromothrips ssp., Echinothrips americanus, Enneothrips flavens, Frankliniella spp. such as F. fusca, F. occidentalis, F. tritici; Heliothrips spp., Hercinothrips femoralis, Kakothrips spp., Microcephalothrips abdominalis, Neohydatothrips samayunkur, Pezothrips kellyanus, Rhipiphorothrips cruentatus, Scirtothrips spp. such as S. citri, S. dorsalis, S. perseae; Stenchaetothrips spp, Taeniothrips cardamoni, Taeniothrips inconsequens, Thrips spp. such as T. imagines, T. hawaiiensis, T. oryzae, T. palmi, T. parvispinus, T. tabaci;

insects of the order Hemiptera, for example, Acizzia jamatonica, Acrosternum spp. as A. hilare; Acyrthosipon spp. as A. onobrychis, A. pisum; Adelges laricis, Adelges tsugae, Adelphocoris spp., Like A. rapidus, A. superbus; Aeneolamia spp., Agonoscena spp., Aulacorthum solani, Aleurocanthus woglumi, Aleurodes spp., Aleurodicus disperses, Aleurolobus barodensis, Aleurothrixus spp., Amrasca spp., Anasa tristis, Antestiopsis spp., Auraphidielphlaphiri ., Auraphidielphi phi. nasturtii, Aphis spp. such as A. craccivora, A. fabae, A. forbesi, A. gossypii, A. grossulariae, A. maidiradicis, A. pomi, A. sambuci, A. schneideri, A. spiraecola; Arboridia apicalis, Arilus critatus, Aspidiella spp., Aspidiotus spp., Atanus spp., Aulacaspis yasumatsui, Aulacorthum solani, Bactericera cockerelli ( Paratrioza cockerelli), Bemisia spp. as B. argentifolii, B. tabaci ( Aleurodes tabaci); Blissus spp. as B. leucopterus; Brachycaudus spp. such as B. cardui, B. helichrysi, B. persicae, B. prunicola; Brachycolus spp., Brachycorynella asparagi, Brevicoryne brassicae, Cacopsylla spp. such as C. fulguralis, C. pyricola ( Psylla pin); Calligypona marginata, Calocoris spp., Campylomma livid, Capitophorus horni, Carneocephala fulgida, Cavelerius spp., Ceraplastes spp., Ceratovacuna lanigera, Ceroplastes ceriferus, Cerosipha gossypii, Chaetosiphon fragaelandi, Chionasuki phyllis philanthus, Chionasuki phyllumica, Chionasukiga phonispilacumita, Chionasukiga phonelus , Cimex spp. as C. hemipterus, C. lectularius; Coccomytilus halli, Coccus spp. as C. hesperidum, C. pseudomagnoliarum; Corythucha arcuata, Creontiades dilutus, Cryptomyzus ribis, Chrysomphalus aonidum, Cryptomyzus ribis, Ctenarytaina spatulata, Cyrtopeltis notatus, Dalbulus spp., Dasynus piperis, Dialeurodes spp. as D. citrifolii; Dalbulus maidis, Diaphorina spp. as D. citri; Diaspis spp. as D. bromeliae; Dichelops furcatus, Diconocoris hewetti, Doralis spp., Dreyfusia nordmannianae, Dreyfusia piceae, Drosicha spp., Dysaphis spp. as D. plantaginea, D. pyri, D. radicola; Dysaulacorthum pseudosolani, Dysdercus spp. as D. cingulatus, D. intermedius; Dysmicoccus spp., Edessa spp., Geocoris spp., Empoasca spp. such as E. fabae, E. solana; Epidiaspis leperii, Eriosoma spp. such as E. lanigerum, E. pyricola; Erythroneura spp., Eurygasterspp. as E. integriceps; Euscelis bilobatus, Euschistus spp. such as E. heros, E. impictiventris, E. servus; Fiorinia theae, Geococcus coffeae, Glycaspis brimblecombei, Halyomorpha spp. as H. halys; Heliopeltis spp., Homalodisca vitripennis ( = H. Coagulata), Horcias nobilellus, Hyalopterus pruni, Hyperomyzus lactucae, Icerya spp. as I. purchase; Idiocerus spp., Idioscopus spp., Laodelphax striatellus, Lecanium spp., Lecanoideus floccissimus, Lepidosaphes spp. as L. ulmi; Leptocorisa spp., Leptoglossus phyllopus, Lipaphis erysimi, Lygus spp. as L. hesperus, L. lineolaris, L. pratensis; Maconellicoccus hirsutus, Marchalina hellenica, Macropes excavatus, Macrosiphum spp. as M. rosae, M. avenae, M. euphorbiae; Macrosteles quadrilineatus, Mahanarva fimbriolata, cribraria Megacopta, Megoura viciae, Melanaphis pyrarius, Melanaphis sacchari, Melanocallis (= Tinocallis) caryaefoliae, Metcafiella spp., Metopolophium dirhodum, Monellia costalis, Monelliopsis pecanis, Myzocallis coryli, Murgantia spp., Myzus spp. such as M. ascalonicus, M. cerasi, M. nicotianae, M. persicae, M. varians; Nasonovia ribis-nigri, Neotoxoptera formosana, Neomegalotomus spp, Nephotettix spp. as N. malayanus, N. nigropictus, N. parvus, N. virescens; Nezara spp. as N. viridula; Nilaparvata lugens, Nysius huttoni, Oebalus spp. as O. pugnax; Oncometopia spp., Ortheza praelonga, Oxycaraenus hyalinipennis, Parabemisia myricae, Palliatoria spp., Parthenolecanium spp. as P. corni, P. persicae; Pemphigus spp. as P. bursarius, P. populivenae; Peregrinus maidis, Perkinsiella saccharicida, Phenacoccus spp. as P. aceris, P. gossypii; Phloeomyzus passerinii, Phorodon humuli, Phylloxera spp. such as P. devastatrix, Piesma quadrata, Piezodorus spp. as P. guildinii; Pinnaspis aspidistrae, Planococcus spp. such as P. citri, P. ficus; Prosapia bicincta, Protopulvinaria pyriformis, Psallus seriatus, Pseudacysta persea, Pseudaulacaspis pentagona, Pseudococcus spp. as P. comstocki; Psylla spp. as P. mali; Pteromalus spp., Pulvinaria amygdali, Pyrilla spp., Quadraspidiotus spp., As Q. perniciosus; Quesada gigas, Rastrococcus spp., Reduvius senilis, Rhizoecus americanus, Rhodnius spp., Rhopalomyzus ascalonicus, Rhopalosiphum spp. such as R. pseudobrassicas, R. insertum, R. maidis, R. padi; Sagatodes spp., Sahlbergella singularis, Saissetia spp., Bad Sappaphis, Sappaphis mali, Scaptocoris spp., Scaphoides titanus, Schizaphis graminum, lanuginosa Schizoneura, Scotinophora spp., Selenaspidus articulatus, Sitobion avenae, Sogata spp., Furcifera Sogatella, Solubea insularis, Spissistilus festinus ( = Stictocephala festina), Stephanitis nashi, Stephanitis pyrioides, Stephanitis takeyai, Tenalaphara malayensis, Tetraleurodes perseae, Therioaphis maculate, Thyanta spp. like T. accerra, T. perditor; Tibraca spp., Tomaspis spp., Toxoptera spp. as T. aurantii; Trialeurodes spp. as T. abutilonea, T. ricini, T. vaporariorum; Triatoma spp., Trioza spp., Typhlocyba spp., Unaspis spp. as U. citri, U. yanonensis; and Viteus vitifolii,

Insects of the order Hymenoptera, for example Acanthomyops interjectus, Athalia rosae, Atta spp. such as A. capiguara, A. cephalotes, A. cephalotes, A. laevigata, A. robusta, A. sexdens, A. texana, Bombus spp., Brachymyrmex spp., Camponotus spp. as C. floridanus, C. pennsylvanicus, C. Modoc; Cardiocondyla nuda, Chalibion sp, Crematogaster spp., Dasymutilla occidentalis, Diprion spp., Dolichovespula maculata, Dorymyrmex spp., Dryocosmus kuriphilus, Formica spp., Hoplocampa spp. as H. minuta, H. testudinea; Iridomyrmex humilis, Lasius spp. such as L. niger, Linepithema humile, Liometopum spp., Leptocybe invasa, Monomorium spp. such as M. pharaonis, Monomorium, Nylandria fulva, Pachycondyla chinensis, Paratrechina longicornis, Paravespula spp., such as P. germanica, P. pennsylvanica, P. vulgaris; Pheidole spp. as P. megacephala; Pogonomyrmex spp. such as P. barbatus, P. californicus, Polistes rubiginosa, Prenolepis impairs, Pseudomyrmex gracilis, Schelipron spp., Sirex cyaneus, Solenopsis spp. such as S. geminata, S.invicta, S. molesta, S. richteri, S. xyloni, Sphecius speciosus, Sphexspp., Tapinoma spp. as T. melanocephalum, T. sessile; Tetramoriumspp. such as T. caespitum, T. bicarinatum, Vespa spp. as V. crabro; Vespula spp. as V. squamosal; Wasmannia auropunctata, Xylocopa sp;

Insects of the order Orthoptera for example Acheta domesticus, Calliptamus italicus, Chortoicetes terminifera, Ceuthophilus spp., Diastrammena asynamora, Dociostaurus maroccanus, Gryllotalpa spp. as G. africana, G. gryllotalpa; Gryllus spp., Hieroglyphus daganensis, Kraussaria angulifera, Locusta spp. as L. migratoria, L. pardalina; Melanoplus spp. such as M. bivittatus, M. femurrubrum, M. mexicanus, M. sanguinipes, M. spretus; Nomadacris septemfasciata, Oedaleus senegalensis, Scapteriscus spp., Schistocerca spp. such as S. americana, S. gregaria, Stemopelmatus spp., Tachycines asynamorus, and Zonozerus variegatus;

Pests of the Class Arachnida, for example, Acari, for example, of the families Argasidae, Ixodidae and Sarcoptidae, such as Amblyomma spp. (eg A. americanum, A. variegatum, A. maculatum), Argas spp. as A. persicu), Boophilus spp. such as B. annulatus, B. decoloratus, B. microplus, Dermacentor spp. such as D. silvarum, D. andersoni, D. variabilis, Hyalomma spp. such as H. truncatum, Ixodes spp. such as I. ricinus, I. rubicundus, I. scapularis, I. holocyclus, I. pacificus, Rhipicephalus sanguineus, Ornithodorus spp. such as O. moubata, O. hermsi, O. turicata, Ornithonyssus bacoti, Otobius megnini, Dermanyssus gallinae, Psoroptes spp. such as P. ovis, Rhipicephalus spp. such as R. sanguineus, R. appendiculatus, Rhipicephalus evertsi, Rhizoglyphus spp., Sarcoptes spp. as S. Scabiei; and family Eriophyidae including Acería spp. such as A. sheldoni, A. anthocoptes, Acallitus spp., Aculops spp. such as A. lycopersici, A. pelekassi; Aculus spp. as A. schlechtendali; Colomerus vitis, Epitrimerus pyri, Phyllocoptruta oleivora; Eriophytes ribis and Eriophyes spp. as Eriophyes sheldoni; Family Tarsonemidae including Hemitarsonemus spp., Phytonemus pallidus and Polyphagotarsonemus latus, Stenotarsonemus spp. Steneotarsonemus spinki; Family Tenuipalpidae including Brevipalpus spp. as B. phoenicis; Family Tetranychidae including Eotetranychus spp., Eutetranychus spp., Oligonychus spp., Petrobia latens, Tetranychus spp. such as T. cinnabarinus, T. evansi, T. kanzawai, T, pacificus, T. phaseulus, T. telarius and T. urticae; Bryobia praetiosa; Panonychus spp. such as P. ulmi, P. citri; Metatetranychus spp. and Oligonychus spp. as O. pratensis, O. perseae, Vasates lycopersici; Raoiella indica, Family Carpoglyphidae including Carpoglyphus spp .; Penthaleidae spp. such as Halotydeus destructor, Family Demodicidae with species such as Demodex spp .; Trombicidea family including Trombicula spp .; Family Macronyssidae including Ornothonyssus spp .; Family Pyemotidae including Pyemotes tritici; Tyrophagus putrescentiae; Family Acaridae including Acarus siro; Araneida family including Latrodectus mactans, Tegenaria agrestis, Chiracanthium sp, Lycosa sp Achaearanea tepidariorum and Loxosceles reclusa;

Pests of the Phylum Nematoda, eg plant parasitic nematodes such as root knot nematodes, Meloidogyne spp. such as M. hapla, M. incognita, M. javanica; cyst- forming nematodes Globodera spp. as G. rostochiensis; Heterodera spp. as H. avenae, H. glycines, H. schachtii, H. trifolii; seed gall nematodes Anguina spp .; Stem and foliar nematodes Aphelenchoides spp. as A. besseyi; Stinging nematodes Belonolaimus spp. as B. tongicaudatus; Pine nematodes Bursaphelenchus spp. such as B. lignicolus, B. xylophilus; ring nematodes Criconema spp., Criconemella spp. as C. xenoplax and C. ornata; and, Criconemoides spp. as Criconemoides informis; Mesocriconema spp .; stem and bulb nematodes, Ditylenchus spp. as D. destructor, D. dipsaci; stinging nematodes Dolichodorus spp .; spiral nematodes Heliocotylenchus multicinctus; Sheath and pod nematodes Hemicycliophora spp. and Hemicriconemoides spp .; Hirshmanniella spp .; Spear nematodesHoploaimus spp .; False root knot nematodes Nacobbus spp .; needle nematodes Longidorus spp. as L. elongatus; lesion nematodes Pratylenchus spp. such as P. brachyurus, P. neglectus, P. penetrans, P. curvitatus, P. goodeyi; Burrowing nematodes, Radopholus spp. as R. similis; Rhadopholus spp .; Rhodopholus spp .; Reniform nematodes Rotylenchus spp. such as R. robustus, R. reniformis; Scutellonema spp .; stubby root nematode Trichodorus spp. as T. obtusus, T. primitivus; Paratrichodorus spp. as P. minor; acrobatic nematodes Tylenchorhynchus spp. such as T. claytoni, T. dubius; citrus nematodes Tylenchulus spp. as T. semipenetrans; dagger nematodes Xiphinema spp .; and other species of plant parasitic nematodes;

Insects of the order Isoptera for example Calotermes flavicollis, Coptotermes spp. as C. formosanus, C. gestroi, C. acinaciformis; Cornitermes cumulans, Cryptotermes spp. as C. brevis, C. cavifrons; Globitermes sulfureus, Heterotermes spp. as H. aureus, H. longiceps, H. tenuis; Leucotermes flavipes, Odontotermes spp., Incisitermes spp. such as I. minor, I. Snyder, Marginitermes hubbardi, Mastotermes spp. such as M. darwiniensis Neocapritermes spp. as N. opacus, N. parvus; Neotermes spp., Procornitermes spp., Zootermopsis spp. such as Z. angusticollis, Z. nevadensis, Reticulitermes spp. such as R. hesperus, R. tibialis, R. speratus, R. flavipes, R. grassei, R. lucifugus, R. santonensis, R. virginicus; Termes natalensis, Insects of the order Blattaria for example Blatta spp. as B. orientalis, B. lateralis; Blattella spp. as B. asahinae, B. germanica; Leucophaea maderae, Panchlora nivea, Periplaneta spp. such as P. americana, P. australasiae, P. brunnea, P. fuligginosa, P. japonica; Supella longipalpa, Parcoblatta pennsylvanica, Eurycotis floridana, Pycnoscelus surinamensis, Insects of the order Siphonoptera for example Cediopsylla simples, Ceratophyllus spp., Ctenocephalides spp. such as C. felis, C. canis, Xenopsylla cheopis, Pulex irritans, Trichodectes canis, Tunga penetrans, and Nosopsyllus fasciatus,

Insects of the order Thysanura, for example, Lepisma saccharina, Ctenolepisma urban, and Thermobia domestica, Pests of the class Chilopoda, for example, Geophilus spp., Scutigera spp. as Scutigera coleoptrata;

Pests of the class Diplopoda for example, Blaniulus guttulatus, Julus spp., Narceus spp.,

Pests of the class Symphyla for example, Scutigerella immaculata,

Insects of the order Dermaptera, for example, Forficula auricularia,

Insects of the order Collembola , for example, Onychiurus spp., Such as Onychiurus armatus,

Pests of the order Isopoda for example, Armadillidium vulgare, Oniscus asellus, Porcellio scaber,

Insects of the order Phthiraptera , for example Damalinia spp., Pediculus spp. What

Pediculus humanus capitis, Pediculus humanus corporis, Pediculus humanus humanus; Pthirus pubis, Haematopinus spp. as Haematopinus eurysternus, Haematopinus suis; Linognathus spp. as Linognathus vituli; Bovicola bovis, Menopon gallinae, Menacanthus stramineus and Solenopotes capillatus, Trichodectes spp. Examples of other pest species that can be controlled by compounds of formula (I) include: from the Phylum Mollusca, class Bivalvia, for example, Dreissena spp .; Gastropoda class, for example, Arion spp., Biomphalaria spp., Bulinus spp., Deroceras spp., Galba spp., Lymnaea spp., Oncomelania spp., Pomacea canaliclata, Succinea spp .; class of helminths, for example, Ancylostoma duodenale, Ancylostoma ceylanicum, Acylostoma braziliensis, Ancylostoma spp., Ascaris lubricoides, Ascaris spp., Brugia malayi, Brugia timori, Bunostomum spp., Chabertia spp., Clonorchis spp., Cooperia spp ., Dicrocoelium spp., Dictyocaulus filaria, Diphyllobothrium latum, Dracunculus medinensis, Echinococcus granulosus, Echinococcus multilocularis, Enterobius vermicularis, Faciola spp., Haemonchus spp. as Haemonchus contortus; Heterakis spp., Hymenolepis nana, Hyostrongulus spp., Loa Loa, Nematodirus spp., Oesophagostomum spp., Opisthorchis spp., Onchocerca volvulus, Ostertagia spp., Paragonimus spp., Schistosomen spp., Strongyloides sterile and fuelleborni Str. ., Taenia saginata, Taenia solium, Trichinella spiralis, Trichinella nativa, Trichinella britovi, Trichinella nelsoni, Trichinella pseudopsiralis, Trichostrongulus spp., Trichuris trichuria, Wuchereria bancrofti.

In one embodiment, the pests are nematodes.

In one embodiment, the nematodes are Meloidogyne sp. such as M. hapla, M. incognita, M. javanica; Cyst-forming nematodes Globodera sp. as G. rostochiensis; Heterodera sp. as H. avenae, H. glycines, H. schachtii, H. trifolii; or seed gall nematodes such as Anguina spp .. In yet another embodiment, the nematodes are Meloidogyne sp., Heterodera sp., or Globodera sp .. In yet another embodiment, the nematodes are Meloidogyne sp .. In yet another embodiment, the nematodes are Heterodera sp. In yet another embodiment, the nematodes are Globodera sp. In yet another embodiment, the nematodes are Meloidogyne incognita, Meloidogyne acrita, or Heterodera glycines. In one embodiment, the method is applied to control pests, while the pests are nematodes selected from the group consisting of Meloidogyne spp., Heterodera spp., Pratylenchus spp., Longidorus spp., Belonolaimus spp. and Globodera spp.

The pesticidal compositions are effective on both contact and ingestion. Furthermore, the compounds of the present invention can be applied to any and all stages of development, such as egg, larva, pupa, and adult.

The compounds and mixtures of the present invention can be applied as such or in the form of compositions comprising them as defined above. In one embodiment, the agrochemical composition comprises at least one auxiliary mixture and one pesticidal mixture as defined above. Furthermore, the compounds of the present invention can be applied together with a mixing partner as defined above or in the form of compositions comprising such mixtures as defined above. The components of said mixture can be applied simultaneously, that is, jointly or separately, or in succession, which is immediately one after the other and thus creating the mixture "in situ" in the desired location, for example, the plant, the sequence, in the case of a separate application, generally has no effect on the result of the control measures. In one embodiment, the pesticidal mixture is applied simultaneously, ie together or separately, or in succession.

The application can be carried out both before and after the infestation of crops, plants, plant propagation materials, such as seeds, soil or the area, material or environment by the pests.

Suitable application methods include, but are not limited to, soil treatment, seed treatment, furrow application, and foliar application. Soil treatment methods include soaking the soil, drip irrigation (drip application over the soil), immersion of roots, tubers, or bulbs, or injection of soil. Seed treatment techniques include seed coating, seed coating, seed powder, seed soaking, and seed granulation. In furrow applications, these generally include the steps of making a furrow in cultivated land, sowing the furrow with seeds, applying the active pesticidal compound to the furrow, and closing the furrow. Foliar application refers to the application of the pesticidal active compound to the foliage of the plant, for example, through spray equipment. For foliar applications, it may be advantageous to modify pest behavior by using pheromones in combination with the compounds of the present invention. Suitable pheromones for specific crops and pests are known to a skilled person and are publicly available from pheromone and semi-chemical databases such as http://www.pherobase.com. As used herein, the term "contact" includes both direct contact (applying the pesticidal mixtures / compositions directly on the animal or plant pest - typically to the foliage, stem or roots of the plant) and indirect contact (applying the pesticidal mixtures / compositions to the locus, i.e., habitat, breeding ground, plant, seed, soil, area, material or environment where a pest, of the animal pest or plant grows or may grow).

The term "animal pest" includes arthropods, gastropods, and nematodes. Preferred animal pests according to the invention are arthropods and nematodes, preferably insects and nematodes, in particular nematodes. The term "crop" refers to both growing and harvested crops.

The term "plant" includes cereals, for example, durum wheat and other wheat, rye, barley, tritical, oats, rice or corn (fodder corn and sugar corn / sweet and field corn); beets, for example sugar beets or fodder beets; fruits, such as pommel, stone fruit, or soft fruit, for example apples, pears, plums, peaches, nectarines, almonds, cherries, papayas, strawberries, raspberries, blackberries, or gooseberries; plants legumes, such as beans, lentils, peas, alfalfa, or soybeans; oil plants, such as rapeseed (oilseed rape), turnip, mustard, olives, sunflowers, coconut, cocoa beans, castor oil plants, oil palms, ground nuts or soybeans; cucurbits, such as squash, squash, cucumber, or melons; fiber plants, such as cotton, flax, hemp or jute; citrus fruits, such as oranges, lemons, grapefruits, or tangerines; vegetables, such as eggplant, spinach, lettuce (for example, iceberg lettuce), chicory, cabbage, asparagus, cabbage, carrots, onions, garlic, leeks, tomatoes, potatoes, cucurbits, or sweet peppers; lauraceae plants, such as avocados, cinnamon, or camphor; power plants and raw materials, such as corn, soybeans, rapeseed, sugar cane or oil palm; tobacco; walnuts, for example, brown pistachios; tea; bananas; vines (table grapes and grape juice vines); jump; sweet leaf (also called Stevia); natural rubber plants or ornamental and forest plants, such as flowers (for example, carnations, petunias, geraniums / pelargoniums, pansies and impatiens), shrubs, broad-leaved trees (for example, poplars), or evergreens, for example conifers eucalyptus; pasture; grass; grass as grass for animal feed or ornamental uses. Preferred plants include potatoes, sugar beets, tobacco, wheat, rye, barley, oats, rice, corn, cotton, soybeans, rapeseed, legumes, sunflowers, coffee, or sugar cane; vines; ornamental; or vegetables, such as cucumbers, tomatoes, beans, or squash.

In one embodiment, the plants are wheat, corn, barley, oats, rye, rice, soybeans, cotton, sugar beet, rapeseed, and potato. In another embodiment, the plants are cotton, soybeans, and corn. In another embodiment, the plants are cotton and soy. In one embodiment, the plants are selected from the group consisting of corn, soybeans, cotton, wheat, barley, and canola. In one embodiment, the plants are selected from the group consisting of carrots, cucurbits, eggplant, melon, onion, garlic, pepper, potato, sweet potato, and tomato. In one embodiment, the plants are selected from the group consisting of coffee, peanuts, peanuts, sugar cane, sunflower, tobacco, and sugar beet. In one embodiment, the plants are selected from the group consisting of banana, citrus, grape, strawberry, almond, pome fruit, and stone fruit.

In one embodiment, the pesticidal mixture is applied to the plants or their propagating material selected from the group consisting of agricultural, forestry and horticultural plants, each in its natural or genetically modified form.

The term "plant" is to be understood to include wild-type plants and plants, which have been modified by conventional breeding, mutagenesis or genetic engineering, or by a combination thereof.

Plants, which have been modified by mutagenesis or genetic engineering, and are of particular commercial importance, include alfalfa, rapeseed (e.g. oilseed rape), beans, carnation, chicory, cotton, eggplant, eucalyptus, flax, lentils, corn, melon, papaya, petunia, plum, poplar, potato, rice, soybean, pumpkin, sugar beet, sugar cane, sunflower, sweet pepper, tobacco, tomato and cereals (e.g. wheat), in particular corn, soybeans, cotton, wheat and rice. In plants, which have been modified by mutagenesis or genetic engineering, one or more genes have been mutagenized or integrated into the genetic material of the plant. The one or more mutagenized or integrated genes are preferably selected from pat, epsps, cry1Ab, bar, cry1Fa2, cry1Ac, cry34Ab1, cry35AB1, cry3A, cryF, cry1F, mcry3a, cry2Ab2, cry3Bb1, cry1A.105, dfr, barnase, vip3Aa20, dfr, barnase, vip3Aa20, barstar, als, bxn, bp40, asn1 and ppo5. The mutagenesis or integration of one or more genes is carried out to improve certain properties of the plant. Such properties, also known as traits, include abiotic stress tolerance, impaired growth / yield, disease resistance, herbicide tolerance, insect resistance, modified product quality, and pollination control. Of these properties, herbicide tolerance, eg imidazolinone tolerance, glyphosate tolerance or glufosinate tolerance are of particular importance. Several plants have become tolerant to herbicides by mutagenesis, eg Clearfield® oilseed rape is tolerant to imidazolinones, eg imazamox. Alternatively, genetic engineering methods have been used to make plants, such as soybeans, cotton, corn, beets, and rapeseed, tolerant to herbicides, such as glyphosate and glufosinate, some of which are available. commercially under the trade names RoundupReady® (glyphosate) and LibertyLink® (glufosinate). Furthermore, resistance to insects is important, in particular resistance to lepidopteran insects and resistance to coleopteran insects. Resistance to insects is typically achieved by modifying plants by integrating cry and / or vip genes, which were isolated from Bacillus thuringiensis (Bt), and encode the respective Bt toxins. Genetically modified insect resistance plants are commercially available under trade names including WideStrike®, Bollgard®, Agrisure®, Herculex®, YieldGard®, Genuity® and Intacta®. Plants can be modified by mutagenesis or genetic engineering, either in terms of one property (unique traits) or in terms of a combination of properties (accumulated traits). Cumulative traits, for example, the combination of herbicide tolerance and insect resistance is becoming increasingly important. In general, all relevant modified plants in relation to singular or accumulated traits, as well as detailed information on mutagenized or integrated genes and the respective events are available on the websites of the organizations "International Service for the Acquisition of Agri-biotech Applications (ISAAA) "(http://www.isaaa.org/gmapprovaldatabase) and" Center for Environmental Risk Assessment (CERA) "(http://ceragmc.org/GMCropDatabase)

Surprisingly, it has been found that the pesticidal activity of the compounds of the present invention can be enhanced by the insecticidal trait of a modified plant. Furthermore, the compounds of the present invention have been found to be suitable for preventing insects from becoming resistant to the insecticidal trait or for combating pests, which have already become resistant to the insecticidal trait of a modified plant. In addition, Compounds of the present invention are suitable for combating pests, against which the insecticidal trait is not effective, so that a complementary insecticidal activity can be advantageously used.

The term "plant propagation material" refers to all generative parts of the plant, such as seeds and vegetative plant material, such as cuttings and tubers (eg potatoes), that can be used for the multiplication of the plant. This includes seeds, roots, fruits, tubers, bulbs, rhizomes, shoots, suckers, and other parts of plants. Seedlings and young plants can also be included, which will be transplanted after germination or after emergence from the soil. These plant propagation materials can be prophylactically treated with a plant protection compound at or before planting or transplantation.

The term "seed" encompasses seeds and propagules of plants of all kinds, including but not limited to true seeds, seed pieces, shoots, corms, bulbs, fruits, tubers, grains, cuttings, cut shoots and the like, and means in a preferred embodiment true seeds.

The term "active ingredient" refers to substances that are active pesticides per se, or by mixing an auxiliary. The active ingredient generally refers to Bacillus amyloliqefaciens, cis-jasmone or component C for the context of the present invention.

In general, "pesticidally effective amount" means the amount of active ingredient necessary to achieve an observable effect on growth, including the effects of necrosis, death, retardation, prevention and elimination, destruction, or otherwise decrease the occurrence and activity of the target organism. The pesticidally effective amount may vary for the various pesticidal mixtures / compositions used in the invention. A pesticidally effective amount of the pesticide mixtures will also vary according to prevailing conditions, such as the effect and duration of the desired pesticide, the climate, the target species, the location, the mode of application, and the like.

In the case of soil treatment, in the application of furrows or in the place where pests live or nest, the amount of active ingredient varies from 0.0001 to 500 g per 100 m2, preferably from 0.001 to 20 g per 100 m2. For use in the treatment of crop plants, for example, by foliar application, the application rate of the active ingredients of this invention may be in the range of 0.0001 g to 4000 g per hectare, for example, 1 g to 2 kg per hectare or from 1 g to 750 g per hectare, desirably from 1 g to 100 g per hectare, more desirably from 10 g to 50 g per hectare, for example 10 to 20 g per hectare, 20 to 30 g per hectare, 30 to 40 g per hectare, or 40 to 50 g per hectare.

The compounds of the present invention are particularly suitable for use in the treatment of seeds in order to protect the seeds from insect pests, in particular from soil-dwelling insect pests, and the roots and shoots of resulting seedlings against soil pests and foliar insects. Therefore, the present invention also relates to a method for the protection of seeds from insects, in particular of soil insects, and of the roots and shoots of seedlings of insects, in particular of soil and foliar insects, said comprising method treating seeds before sowing and / or after pregermination with a compound of the present invention. Protection of the roots and shoots of the seedlings is preferred. More preferred is the protection of the seedling shoots against boring and sucking insects, chewing insects and nematodes.

The term "seed treatment" encompasses all suitable seed treatment techniques known in the art, such as seed coating, seed coating, seed spraying, seed soaking, seed granulation, and furrow application methods. Preferably, the seed treatment application of the active compound is carried out by sprinkling or spraying the seeds before sowing the plants and before the emergence of the plants.

The present invention also encompasses seeds coated with or containing the active compound. In general, the seeds are coated with the active compounds. The term "coated and / or containing" generally means that the active ingredient is mostly on the surface of the propagation product at the time of application, although a greater or lesser part of the ingredient may penetrate into the propagation product. , depending on the application method. When said propagation product is (re) planted, it can absorb the active ingredient.

Suitable seeds are, for example, cereal seeds, root crops, oil crops, vegetables, spices, ornamental plants, for example seeds of durum wheat and other varieties of wheat, barley, oats, rye, corn (fodder corn and corn sugar / sweet and field corn), soybeans, oil crops, crucifers, cotton, sunflowers, bananas, rice, oilseed rape, turnip, sugar beet, fodder beet, eggplant, potatoes, grass, grass, lawn, fodder, tomatoes, leeks , pumpkin / squash, cabbage, iceberg lettuce, bell pepper, cucumbers, melons, Brassica species, melons, beans, peas, garlic, onions, carrots, tuberous plants such as potatoes, sugar cane, tobacco, grapes, petunias, geraniums / pelargoniums , thoughts and impatiens.

Furthermore, the active compound can also be used for the treatment of plant seeds, which have been modified by mutagenesis or genetic engineering, and which, for example, tolerate the action of herbicides or fungicides or insecticides. Such modified plants have been described in detail above.

Conventional seed treatment formulations include, for example, fluid concentrates FS, solutions LS, suspoemulsions (SE), powders for dry treatment DS, water dispersible powders for treatment of sludge WS, water soluble powders SS and ES and EC emulsion and GF gel formulation. These formulations can be applied to the seed diluted or undiluted. The application to the seeds is carried out before sowing, either directly on the seeds or after having pre-germinated the latter. Preferably, the formulations are applied so that germination is not included.

The active substance concentrations in ready-to-use formulations, which can be obtained after a two to ten-fold dilution, are preferably 0.01 to 60% by weight, more preferably 0.1 to 40% by weight.

In a preferred embodiment, an FS formulation is used for treating seeds. Typically, a FS formulation may comprise 1-800 g / l of active ingredient, 1-200 g / l of surfactant, 0 to 200 g / l of antifreeze agent, 0 to 400 g / l of binder, 0 to 200 g / l of a pigment and up to 1 liter of solvent, preferably water.

Especially preferred FS formulations of the compounds of the present invention for seed treatment generally comprise 0.1 to 80% by weight (1 to 800 g / l) of the active ingredient, 0.1 to 20% by weight (1 to 200 g / l) of at least one surfactant, for example 0.05 to 5% by weight of a humectant and 0.5 to 15% by weight of a dispersing agent, up to 20% by weight, for example 5 to 20% of an agent antifreeze, 0 to 15% by weight, for example 1 to 15% by weight of a pigment and / or a dye, 0 to 40% by weight, for example 1 to 40% by weight of a binder (adhesive / bonding agent), optionally up to 5% by weight, for example 0.1 to 5% by weight of a thickener, optionally 0.1 to 2% of an 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 load / vehicle up to 100% by weight.

In seed treatment, the application rates of the active ingredients of the pesticidal compositions of the invention are generally 0.1 g to 10 kg per 100 kg of seed, preferably 1 to 5 kg per 100 kg of seed, more preferably 1 g to 1000 g per 100 kg of seed, more preferably 1 g to 200 g per 100 kg of seed, and in particular from 1 g to 100 g per 100 kg of seed, for example from 5 g to 50 g per 100 kg of seed. Therefore, the invention also relates to plant propagation material, preferably seeds, comprising the active ingredients of the pesticidal mixtures of the present invention. The amount of the active ingredients of the present invention will generally range from 0.1 g to 10 kg per 100 kg of seed, preferably from 1 to 5 kg per 100 kg of seed, more preferably from 1 to 1000 g per 100 kg of seed, and in particular from 1 g to 100 g per 100 kg of seed. For specific crops like lettuce, the rate may be higher. In one embodiment, the plant propagation material comprises a pesticidal mixture or an agrochemical composition according to the invention. The compounds of the present invention can also be used to improve the health of a plant. Therefore, the present invention also relates to a method of improving plant health by treating a plant, plant propagation material and / or the place where the plant is growing or will grow with an effective amount and not phytotoxicity of a compound of the present invention. As used herein, "an effective and non-phytotoxic amount" means that the compound is used in an amount that allows the desired effect to be obtained but does not give rise to any phytotoxic symptoms in the treated plant or in the plant grown at starting from the treated propagule or treated soil. The terms "plant" and "plant propagation material" are defined above.

"Plant health" is defined as a condition of the plant and / or its products that is determined by several aspects alone or in combination with each other, such as yield (eg increased biomass and / or higher content of valuable ingredients), quality (eg better content or composition of certain ingredients or shelf life), plant vigor (eg better plant growth and / or greener leaves ("green effect"), stress tolerance abiotic (eg drought) and / or biotic (eg disease) and production efficiency (eg harvest efficiency, processability).

The indicators identified above for the health status of a plant can be interdependent and can result from each other. Each indicator is defined in the art and can be determined by methods known to one of skill.

The compounds of the invention are also suitable for use against non-agricultural insect pests. For use against such non-agricultural pests, the pesticidal mixtures of the present invention can be used as a bait composition, gel, general insect spray, aerosol, ultra-low volume application, and bednet (impregnated or applied in bedding). surface). In addition, steeping and steeping methods can be used. As used herein, the term "non-crop insect pest" refers to pests, which they are particularly relevant for non-cultured targets such as ants, termites, wasps, flies, ticks, mosquitoes, grasshoppers, or cockroaches.

The bait can be a liquid, solid or semi-solid preparation (eg, a gel). The bait used in the composition is a product that is attractive enough to incite insects such as ants, termites, wasps, flies, mosquitoes, grasshoppers, etc. or roaches to eat it. The attractiveness can be manipulated using food stimulants or sex pheromones. Food stimulants are chosen, for example, but not exclusively, from animal and / or vegetable proteins (meat, fish or blood meal, insect parts, egg yolk), fats and oils of animal and / or vegetable origin, or mono, oligo or polyorganosaccharides, especially of sucrose, lactose, fructose, dextrose, glucose, starch, pectin or even molasses or honey. Fresh or decaying parts of fruits, crops, plants, animals, insects, or specific parts thereof can also serve as feeding stimulants. Sex pheromones are known to be more insect specific. Specific pheromones are described in the literature (eg http://www.pherobase.com) and are known to those of skill in the art.

For use in bait compositions, typical active ingredient content is 0.001% by weight to 15% by weight, desirably 0.001% by weight to 5% by weight of active compound.

Formulations of the compounds of the present invention as aerosols (for example, in spray cans), oil sprays or pump sprays are well suited for the non-professional user to control pests such as flies, fleas, ticks, mosquitoes or cockroaches. . Aerosol recipes are preferably composed of the active compound, solvents, as well as auxiliaries such as emulsifiers, perfume oils, if they are appropriate stabilizers and, if necessary, propellants.

Oil spray formulations differ from aerosol recipes in that no propellants are used.

For use in spray compositions, the active ingredient content is 0.001 to 80% by weight, preferably 0.01 to 50% by weight, and most preferably 0.01 to 15% by weight.

Pesticide mixtures can also be used in mosquito and spray coils, smoke cartridges, vaporizer plates or long-life vaporizers, and also in moth papers, moth pads, or other heat-independent vaporizer systems.

Methods to control infectious diseases transmitted by insects (for example, malaria, dengue and yellow fever, lymphatic filariasis, and leishmaniasis) with pesticide mixtures also include surface treatment of sentry boxes and houses, air spraying and impregnation of curtains, tents, articles of clothing, mosquito nets, tsetse fly traps or the like. Insecticidal compositions for application to fibers, fabrics, knits, nonwovens, meshes or sheets and canvases preferably comprise a mixture that includes the insecticide, optionally a repellent and at least one binder.

Pesticide mixtures can be used to protect wooden materials such as trees, board fences, sleepers, frames, artifacts, etc. and buildings, but also building materials, furniture, hides, fibers, vinyl articles, electrical cables, etc. ants and / or termites, and to control that ants and termites harm crops or humans (for example, when pests invade homes and public facilities).

Typical application rates in material protection are, for example, 0.001 g to 2000 g or 0.01 g to 1000 g of active compound per m2 of treated material, desirably 0.1 g to 50 g per m2.

Insecticidal compositions for use in impregnating materials typically contain 0.001 to 95% by weight, preferably 0.1 to 45% by weight, and more preferably 1 to 25% by weight of at least one repellent and / or insecticide.

The pesticide mixture can also be used in storage application. In one embodiment of the invention, the pesticidal mixture can be applied to seeds in a storage facility or airtight storage containers. In another embodiment of the invention, the pesticidal mixture can be applied by treating the seed with Bacillus amyloliquefaciens ssp. plantarum strain MBI600 and volatilizing cis-jasmone in the headspace of a storage facility or airtight storage containers. The cis-jasmone volatilization process can be carried out by placing an open container of cis-jasmone in the reservoirs, thermal fogging, microencapsulation delivery devices, aspirators, or any device that generates cis-jasmone.

The following examples illustrate the invention.

To establish whether there is a synergistic effect, the expected efficacy must be calculated and compared with the observed efficacy of the mixture according to the invention.

Synergism 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 percentage of control, between two mixing partners (X and Y) can be calculated using Colby's equation (Colby, SR, 1967, Calculating Synergistic and Antagonistic Responses in Herbicide Combinations, Weeds, 15 , 20-22):

E = XY - ^XY

100

X = Observed efficacy (in% of untreated control) of compound 1

Y = Observed efficacy (in% of untreated control) of compound 2

E = Efficacy calculated (i.e. expected) (in% of untreated control)

When the observed efficacy (%) is greater than the calculated efficacy (E) according to Colby (%), then the combined effect is synergistic.

The following tests demonstrate the control efficacy of pesticide mixtures on specific pests. However, the pest control protection provided by pesticide mixtures is not limited to these species. The analysis of synergy or antagonism between the mixtures or mixtures was determined using the Colby equation.

Example 1:

To evaluate the control of root knot nematodes ( Meloidogyne incognita / acrita) in cotton, cotton seeds (variety PhytoGen PHY 499 WRF) were treated with cis-jasmone, MBI600 ( Bacillus amyloliquefaciens ssp. Plantarum MBI600), or a mixture of them.

The seeds were placed in a plastic cup and the compounds, or their mixture, were dosed into the seeds with an application rate of 0.2 g of cis-jasmone per 100 kg of seeds, and 1 * 1011 CFU of MBI600 per 100 kg of seeds. The seeds were sown in 10 x 30 ft plots with 4 replications in fields infested with root knot nematodes. Crop yields (pounds / acre) were averaged across the four replicates. Those figures were converted into% yields of the untreated control.

Table 1: Performance improvement against root knot nematode in cotton

Example 2

To evaluate the control of soybean cyst nematodes (Heterodera glycines) in soybeans, soybeans (variety Dyna-Gro 39RY43) were treated with cis-jasmone, MBI600 ( Bacillus amyloliquefaciens ssp. Plantarum MBI600), or a mixture of the same.

The seeds were placed in a plastic cup and the compounds, or their mixture, were dosed into the seeds with an application rate of 0.2 g of cis-jasmone per 100 kg of seeds, and 1 * 1011 CFU of MBI600 per 100 kg of seeds. The seeds were sown in 10 x 30 ft plots with 4 replications in fields infested with root knot nematodes. Crop yields (bushels / acre) were averaged across the four replicates. Those figures were converted into% yields of the untreated control.

Table 2: Performance improvement against soybean cyst nematode in soybeans

Example 3:

To evaluate the control of root knot nematodes (Meloidogyne incognita / acrita) in corn, corn seeds (varieties NG6247MQKZ, NF5334MQKZ and NG4549MQKZ, respectively) were treated with cis-jasmona, MBI600 (Bacillus amyloliquefaciens MBI600, plantarum MBI600. Plantarum MBI600. Plantarum MBI600. or a mixture thereof. The seeds were placed in a plastic cup and the compounds, or their mixture, were dosed into the seeds with an application rate of 0.2 g of cis-jasmone per 100 kg of seeds, and 1 * 1011 CFU of MBI600 per 100 kg of seeds. Seeds were sown in 10 x 30 ft plots with 4-6 replicates depending on the test location in the root knot nematode infested fields. Harvest yields ( bushels / acre) were averaged over the 4-6 replicates, these figures were converted into% yields of the untreated control.

Table 3: Performance improvement against root knot nematode in corn

Claims (1)

1. Pesticide mixtures comprising, as active components, Bacillus amyloliquefaciens ssp. plantarum strain MBI600 and cis-jasmone in synergistically effective amounts, where the ratio of Bacillus amyloliquefaciens ssp. The plantarum strain MBI600 a cis-jasmone is 1016 CFU: 1 g to 105 CFU: 1 g. 2. The pesticidal mixtures according to claim 1, wherein the proportion of Bacillus amyloliquefaciens ssp. the plantarum strain MBI600 a cis-jasmone is 1015 CFU: 1 g to 108 CFU: 1 g. The pesticide mixtures according to claim 1 or 2, further comprising a component C selected from the following groups: M Insecticides: M.1 Acetylcholine esterase inhibitors: M.1A carbamates: aldicarb, alanicarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formethanate, furathiocarb, isoprocarb, methiocarb, methomyoxycarbamyl, thioxycarbonate, trimethylcarbonate, trimethylcarbonate , XMC, xylylcarb, and triazamate; Y M.1B Organophosphates: acefate, azamethiphos, azinphos-ethyl, azinphosmethyl, cadusaphos, chlorethoxyphos, chlorfenvinphos, chloromephos, chlorpyrifos, chlorpyrifos-methyl, coumaphos, cyanophos, demeton-S-methyl, diazinon, dichlorvos / dimethylV dimethylP, dichrothoxyphos, Dichlorvos / dimethylV dimethylP , disulfoton, EPN, ethion, ethoprophos, fampur, fenamiphos, fenitrothion, fenthion, phostiazate, heptenophos, imitiaphos, isophenphos, isopropyl O- (methoxyaminophosphoryl) salicylate, isoxation, malathion, mecarbam, methamidophos, methosphos, methidation , omethoate, oxydemeton-methyl, parathion, parathion-methyl, pentoate, phorate, fosalone, phosmet, phosphamidon, phoxim, pyrimiphos-methyl, prophenophos, propetamphos, protiophos, pyraclophos, pyridaphenthion, quinalphos, sulfotep, temebuphosorimphos, tetraphosphosphosphosphosphosphate , thiometon, triazophos, trichlorfon and vamidothion; M.2 GABA-activated chloride channel antagonists: M.2A Organochlorine cyclodiene compounds: endosulfan or chlordane; Y M.2B Fiprole: ethiprole, fipronil, flufiprole, pyrafluprole and pyriprole; M.3 Sodium channel modulators: M.3A pyrethroids: acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin, bifenthrin, bioalethrin, bioalethrin S-cyclopentenyl, bioresmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, alpha cyhalothrin, gamma cyhalothrin -cypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin, deltamethrin, empenthrin, sphenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate, flumethrin, tau-fluxluvalinate, im- methrothrin, methofluiprin, methofluiprine, methofluiprine, methofluiprine, methofluiprine, methofluiprine, methofluiprine, methofluiprine , phenothrin, pralethrin, profluthrin, pyrethrin (pyrethrum), resmethrin, silafluofen, tefluthrin, tetramethylfluthrin, tetramethrin, tralomethrin, and transfluthrin; and M.3B Sodium channel modulators: DDT and methoxychlor; M.4 Nicotinic acetylcholine receptor agonists: M.4A.1 Neonicotinoids: acetamiprid, clothianidin, cycloxaprid, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam; M.4A.2 (2E -) - 1 [(6-Chloropyridin-3-yl) methyl] -N'-nitro-2-pentylidenehydrazine-carboximidamide; M4.A.31 - [(6-Chloropyridin-3-yl) methyl] -7-methyl-8-nitro-5-propoxy-1,2,3,5,6,7-hexahydroimidazo [1,2-a ] pyridine; and M.4B nicotine; M.5 Allosteric activators of the nicotinic acetylcholine receptor of the spinosyn class: spinosad and spinetoram; M.6 Activators of chloride channels of the avermectin and milbemycin class: abamectin, emamectin benzoate, ivermectin, lepimectin and milbemectin; M.7 Juvenile hormone mimics: M.7A Juvenile Hormone Analogs: Hydroprene, Kinoprene, and Methoprene; Y M.7B fenoxycarb and pyriproxyfen; M.8 Miscellaneous non-specific inhibitors: M.8A Alkyl halides: methyl bromide and other alkyl halides; Y M.8B chloropicrin, sulfuryl fluoride, borax and tartar emetic; M.9 Selective blockers of homopterana feeding: pymetrozine and flonicamid; M.10 Mite growth inhibitors: clofentezine, hexythiazox, diflovidazine and ethoxazole; M.11 Microbial disruptors of the intestinal membranes of the insect: Bacillus thuringiensis, Bacillus sphaericus and the insecticidal proteins that they produce: Bacillus thuringiensis subsp. israelensis, Bacillus sphaericus, Bacillus thuringiensis subsp. aizawai, Bacillus thuringiensis subsp. Kurstaki and Bacillus thuringiensis subsp. tenebrionis, or the Bt culture proteins: Cry1Ab, Cry1Ac, Cry1Fa, Cry2Ab, mCry3A, Cry3Ab, Cry3Bb and Cry34 / 35Ab1; M.12 Mitochondrial ATP synthase inhibitors: M.12A diaphenthuron, and organotin miticides: azocyclotin, cyhexatin, and fenbutatin oxide; Y M.12B propargite and tetradiphon; M.13 Oxidative phosphorylation decouplers through proton gradient disruption: chlorfenapir, DNOC, and sulfluramide; M.14 Nicotinic acetylcholine receptor channel blockers: bensultap, cartap hydrochloride, thiocyclam, and tiosultap sodium; M.15 Type 0 chitin biosynthesis inhibitors: bistrifluron, chlorfluazuron, diflubenzuron, flucIcloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron and triflumuron; M.16 Type 1 chitin biosynthesis inhibitors: buprofezin; M.17 molt disruptors: chromazine; M.18 Ecdyson receptor agonists: methoxyphenozide, tebufenozide, halofenozide, fufenozide, or chromafenozide; M.19 Octopamine receptor agonists: amitraz; M.20 Inhibitors of electron transport of mitochondrial complex III: hydramethylnon, acequinocyl and fluacripirim; M.21 Inhibitors of electron transport of mitochondrial complex I: M.21A METI acaricides and insecticides: fenazaquin, fenpyroximate, pyrimidiphene, pyridaben, tebufenpyrad and tolfenpyrad; and M.21B rotenone; M.22 Voltage-gated sodium channel blockers: M.22A indoxacarb; M.22B metaflumizone; M.22B.1 2- [2- (4-Cyanophenyl) -1- [3- (trifluoromethyl) phenyl] ethylidene] -N- [4- (difluoromethoxy) phenyl] -hydrazinecarboxamide; M.22B.2 N- (3-Chloro-2-methylphenyl) -2 - [(4-chlorophenyl) [4- [methyl (methylsulfonyl) amino] phenyl] methylene] -hydrazinecarboxamide; M.23 Acetyl CoA carboxylase inhibitors of the class of tetronic and tetramic acid derivatives: spirodiclofen, spiromesifene and spirotetramat; M.24 Inhibitors of electron transport of mitochondrial complex IV: M.24A Phosphorous compounds: aluminum phosphide, calcium phosphide, phosphine and zinc phosphide; Y M.24B Cyanide; M.25 Mitochondrial complex II electron transport inhibitors of the class of beta-acetonitrile derivatives: Cenopirafen and Cyflumetofen; M.28 Diamide class ryanodine receptor modulators: flubendiamide, chlorantraniliprole (rynaxypyr®), cyantraniliprole (cyazypyr®), tetranyliprole; and phthalamide compounds; M.28.1 (R) -3-Chloro-N1- {2-methyl-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] phenyl} -N2- (1-methyl-2- methylsulfonylethyl) phthalamide; 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; M.28.3 3-bromo-N- {2-bromo-4-chloro-6 - [(1-cyclopropylethyl) carbamoyl] phenyl} -1- (3-chlorpyridin-2-yl) -1H-pyrazole-5-carboxamide (proposed ISO name: cyclaniliprole); M.28.4 methyl-2- [3,5-dibromo-2 - ({[3-bromo-1- (3-chlorpyridin-2-yl) -1H-pyrazol-5-yl] carbonyl} amino) benzoyl] - 1,2-dimethylhydrazinecarboxylate; M.28.5a N- [4,6-dichloro-2 - [(diethyl-lambda-4-sulfanylidene) carbamoyl] -phenyl] -2- (3-chloro-2-pyridyl) -5- (trifluoromethyl) pyrazole- 3-carboxamide; M.28.5b N- [4-chloro-2 - [(diethyl-lambda-4-sulfanylidene) carbamoyl] -6-methyl-phenyl] -2- (3-chloro-2-pyridyl) -5- (trifluoromethyl) pyrazole-3-carboxamide; M.28.5c N- [4-chloro-2 - [(di-2-propyl-lambda-4-sulfanylidene) carbamoyl] -6-methyl-phenyl] -2- (3-chloro-2-pyridyl) -5 - (trifluoromethyl) pyrazole-3-carboxamide; M.28.5d N- [4,6-dichloro-2 - [(di-2-propyl-lambda-4-sulfanylidene) carbamoyl] -phenyl] -2- (3-chloro-2-pyridyl) -5- ( trifluoromethyl) pyrazole-3-carboxamide; M.28.5h N- [4,6-dibromo-2 - [(diethyl-lambda-4-sulfanylidene) carbamoyl] -phenyl] -2- (3-chloro-2-pyridyl) -5- (trifluoromethyl) pyrazole- 3-carboxamide; M.28.5i N- [2- (5-Amino-1,3,4-thiadiazol-2-yl) -4-chloro-6-methylphenyl] -3-bromo-1- (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] carbonyl] phenyl] -1H -pyrazole-5-carboxamide; M.28.5k 3-Bromo-N- [2,4-dichloro-6- (methylcarbamoyl) phenyl] -1- (3,5-dichloro-2-pyridyl) -1H-pyrazole-5-carboxamide; M.28.5l N- [4-Chloro-2 - [[(1,1-dimethylethyl) amino] carbonyl] -6-methylphenyl] -1- (3-chloro-2-pyridinyl) -3- (fluoromethoxy) - 1H-pyrazole-5-carboxamide; Y M.28.6: cylodiamide; M.29. insecticidal active compounds of unknown or uncertain mode of action: afidopiropen, afoxolaner, azadirachtin, amidoflumet, benzoximate, biphenazate, broflanilide, bromopropylate, chinomethionate, cryolite, dichloromezothiaz, dicofol, flufenerim, flomethoquin, flluexaphuronezone, flluexaphurifonazuphone, fllueupheuriflazone from piperonyl, pirflubumide, pyridylyl, pyrifluquinazon, sulfoxaflor, thioxazafen, and triflumezopyrim; M.29.3 11- (4-chloro-2,6-dimethylphenyl) -12-hydroxy-1,4-dioxa-9-azadispiro [4.2.4.2] -tetradec-11-en-10-one; M.29.4 3- (4'-fluoro-2,4-dimethylbiphenyl-3-yl) -4-hydroxy-8-oxa-1-azaspiro [4.5] dec-3-en-2-one; M.29.5 1- [2-fluoro-4-methyl-5 - [(2,2,2-trifluoroethyl) sulfinyl] phenyl] -3- (trifluoromethyl) -1H-1,2,4-triazol-5-amine and active compounds based on Bacillus firmus (Votivo, I-1582); Y M.29.6a (E / Z) -N- [1 - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2,2-trifluoroacetamide; M.29.6b (E / Z) -N- [1 [(6-chloro-5-fluoro-3-pyridyl) methyl] -2-pyridylidene] -2,2,2-trifluoro-acetamide; M.29.6c (E / Z) -2,2,2-trifluoro-N- [1 [(6-fluoro-3-pyridyl) methyl] -2-pyridylidene] acetamide; M.29.6d (E / Z) -N- [1 - [(6-bromo-3-pyridyl) methyl] -2-pyridylidene] -2,2,2-trifluoroacetamide; M.29.6e (E / Z) -N- [1- [1- (6-chloro-3-pyridyl) ethyl] -2-pyridylidene] -2,2,2-trifluoroacetamide; M.29.6f (E / Z) -N- [1 - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2-difluoro-acetamide; M.29.6g (E / Z) -2-chloro-N- [1 - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2-difluoro-acetamide; M.29.6h (E / Z) -N- [1 - [(2-chloropyrimidin-5-yl) methyl] -2-pyridylidene] -2,2,2-trifluoroacetamide; M.29.6i (E / Z) -N- [1 - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2,3,3,3-pentafluoro-propanamide); M.29.6j N- [1 - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2,2-trifluoro-thioacetamide; Y M.29.6k N- [1 - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -2,2,2-trifluoro-N'-isopropyl-acetamidine; M.29.8 fluazaindolizine; M.29.9a 4- [5- (3,5-dichlorophenyl) -5- (trifluoromethyl) -4H-isoxazol-3-yl] -2-methyl-N- (1-oxothietan-3-yl) benzamide; Y M.29.9b fluxamethamide; M.29.105- [3- [2,6-dichloro-4- (3,3-dydoroallyloxy) phenoxy] propoxy] -1H-pyrazole; M.29.11b 3- (benzoylmethylamino) -N- [2-bromo-4- [1,2,2,3,3,3-hexafluoro-1- (trifluoromethyl) propyl] -6- (trifluoromethyl) phenyl] - 2-fluoro-benzamide; M.29.11c 3- (benzoylmethylamino) -2-fluoro-N- [2-iodo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- (trifluoromethyl) feml] - benzamide; M.29.11d N- [3 - [[[2-iodo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- (trifluoromethyl) phenyl] amino] carbonyl] phenyl] -N-methylbenzamide; M.29.11e N- [3 - [[[2-bromo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- (trifluoromethyl) phenyl] amino] carbonyl] -2 -fluorophenyl] -4-fluoro-N-methyl-benzamide; M.29.11f 4-fluoro-N- [2-fluoro-3 - [[[2-iodo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- (trifluoromethyl) phenyl] amino] carbonyl] phenyl] -N-methyl-benzamide; M.29.11g 3-fluoro-N- [2-fluoro-3 - [[[2-iodo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- (trifluoromethyl) phenyl] amino] carbonyl] phenyl] -N-methyl-benzamide; M.29.11h 2-chloro-N- [3 - [[[2-iodo-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] -6- (trifluoromethyl) phenyl] amino] carbonyl] phenyl] -3-pyridinecarboxamide; M.29.11 i 4-cyano-N- [2-cyano-5 - [[2,6-dibromo-4- [1,2,2,3,3,3-hexafluoro-1- (trifluoromethyl) propyl] femlo ] carbamoyl] feml] -2-methyl-benzamide; M.29.11j 4-cyano-3 - [(4-cyano-2-methyl-benzoyl) amino] -N- [2,6-dichloro-4- [1,2,2,3,3,3-hexafluoro -1- (trifluoromethyl) propyl] phenyl] -2-fluoro-benzamide; M.29.11k N- [5 - [[2-chloro-6-cyano-4- [1,2,2,3,3,3-hexafluoro-1- (trifluoromethyl) propyl] -phenyl] carbamoyl] -2 -cyano-phenyl] -4-cyano-2-methyl-benzamide; M.29.111 N- [5 - [[2-bromo-6-chloro-4- [2,2,2-trifluoro-1-hydroxy-1- (trifluoromethyl) ethyl] -phenyl] carbamoyl] -2-cyano- phenyl] -4-cyano-2-methyl-benzamide; M.29.11m N- [5 - [[2-bromo-6-chloro-4- [1,2,2,3,3,3-hexafluoro-1- (trifluoromethyl) -propyl] phenyl] carbamoyl] -2 -cyano-phenyl] -4-cyano-2-methyl-benzamide; M.29.11n 4-cyano-N- [2-cyano-5 - [[2,6-dichloro-4- [1,2,2,3,3,3-hexafluoro-1- (trifluoromethyl) propyl] phenyl] ] carbamoyl] phenyl] -2-methyl-benzamide; M.29.11o 4-cyano-N- [2-cyano-5 - [[2,6-dichloro-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] phenyl] carbamoyl] phenyl ] -2-methylbenzamide; M.29.11p N- [5 - [[2-bromo-6-chloro-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] phenyl] -carbamoyl] -2-cyano-phenyl ] -4-cyano-2-methyl-benzamide; M.29.12a 2- (1,3-Dioxan-2-yl) 6- [2- (3-pyridinyl) -5-thiazolyl] -pyridine; M.29.12b 2- [6- [2- (5-Fluoro-3-pyridinyl) -5-thiazolyl] -2-pyridinyl] -pyrimidine; M.29.12c 2- [6- [2- (3-pyridinyl) -5-thiazolyl] -2-pyridinyl] -pyrimidine; M.29.12d N-methylsulfonyl-6- [2- (3-pyridyl) thiazol-5-yl] pyridine-2-carboxamide; M.29.12e N-methylsulfonyl-6- [2- (3-pyridyl) thiazol-5-yl] pyridine-2-carboxamide; M.29.12f N-Ethyl-N- [4-methyl-2- (3-pyridyl) thiazol-5-yl] -3-methylthio-propanamide; M.29.12g N-Methyl-N- [4-methyl-2- (3-pyridyl) thiazol-5-yl] -3-methylthio-propanamide; M.29.12h N, 2-Dimethyl-N- [4-methyl-2- (3-pyridyl) thiazol-5-yl] -3-methylthio-propanamide; M.29.12i N-Ethyl-2-methyl-N- [4-methyl-2- (3-pyridyl) thiazol-5-yl] -3-methylthio-propanamide; M.29.12j N- [4-chloro-2- (3-pyridyl) thiazol-5-yl] -N-ethyl-2-methyl-3-methylthio-propanamide; M.29.12k N- [4-chloro-2- (3-pyridyl) thiazol-5-yl] -N, 2-dimethyl-3-methylthio-propanamide; M.29,121 N- [4-chloro-2- (3-pyridyl) thiazol-5-yl] -N-methyl-3-methylthio-propanamide; M.29.12m N- [4-chloro-2- (3-pyridyl) thiazol-5-yl] -N-ethyl-3-methylthio-propanamide; or the compounds M.29.14a 1 - [(6-Chloro-3-pyridinyl) methyl] -1,2,3,5,6,7-hexahydro-5-methoxy-7-methyl-8-nitro-imidazo [1,2 -a] pyridine; M.29.14b 1 - [(6-Chloropyridin-3-yl) methyl] -7-methyl-8-nitro-1,2,3,5,6,7-hexahydroimidazo [1,2-a] pyridin-5 -ol; M.29.16.a 1-isopropyl-N, 5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; or M.29.16b 1- (1,2-dimethylpropyl) -N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.16c N, 5-dimethyl-N-pyridazin-4-yl-1- (2,2,2-trifluoro-1-methyl-ethyl) pyrazole-4-carboxamide; M.29.16d 1- [1- (1-cyanocyclopropyl) ethyl] -N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.16e N-ethyl-1- (2-fluoro-1-methyl-propyl) -5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.16f 1- (1,2-dimethylpropyl) -N, 5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.16g 1- [1- (1-cyanocyclopropyl) ethyl] -N, 5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.16h N-methyl-1- (2-fluoro-1-methyl-propyl] -5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.16i 1- (4,4-difluorocyclohexyl) -N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; Y M.29.16j 1- (4,4-difluorocyclohexyl) -N, 5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide; M.29.17a N- (1-methylethyl) -2- (3-pyridinyl) -2H-indazole-4-carboxamide; M.29.17b N-cyclopropyl-2- (3-pyridinyl) -2H-indazole-4-carboxamide; M.29.17c N-cyclohexyl-2- (3-pyridinyl) -2H-indazole-4-carboxamide; M.29.17d 2- (3-pyridinyl) -N- (2,2,2-trifluoroethyl) -2H-indazole-4-carboxamide; M.29.17e 2- (3-pyridinyl) -N - [(tetrahydro-2-furanyl) methyl] -2H-indazole-5-carboxamide; M.29.17f methyl 2 - [[2- (3-pyridinyl) -2H-indazol-5-yl] carbonyl] hydrazinecarboxylate; M.29.17g N - [(2,2-difluorocyclopropyl) methyl] -2- (3-pyridinyl) -2H-indazole-5-carboxamide; M.29.17h N- (2,2-difluoropropyl) -2- (3-pyridinyl) -2H-indazole-5-carboxamide; M.29.17i 2- (3-pyridinyl) -N- (2-pyrimidinylmethyl) -2H-indazole-5-carboxamide; Y M.29.17j N - [(5-methyl-2-pyrazinyl) methyl] -2- (3-pyridinyl) -2H-indazole-5-carboxamide; M.29.18a N- [3-chloro-1- (3-pyridyl) pyrazol-4-yl] -N-ethyl-3- (3,3,3-trifluoropropylsulfanyl) -propanamide; M.29.18b N- [3-chloro-1- (3-pyridyl) pyrazol-4-yl] -N-ethyl-3- (3,3,3-trifluoropropylsulfinyl) -propanamide; M.29.18c N- [3-chloro-1- (3-pyridyl) pyrazol-4-yl] -3 - [(2,2-difluorocyclopropyl) -methylsulfanyl] -N-ethyl-propanamide; Y M.29.18d N- [3-chloro-1 - (3-pyridyl) pyrazol-4-yl] -3 - [(2,2-difluorocyclopropyl) -methylsulfinyl] -N-ethyl-propanamide; M.29.19 sarolaner; M.29.20 lotilaner; L Biopesticides: L.1 Microbial pesticides with fungicidal, bactericidal, viricidal and / or activating plant defense activity: Ampelomyces quisqualis, Aspergillus flavus, Aureobasidium pullulans, Bacillus altitudinis, B. megaterium, B. mojavensis, B. mycoides, B. simplex, B. solisalsi, B. subtilis, Candida oleophila, C. saitoana, Clavibacter michiganensis (bacteriophages), Coniothyrium minitans, Cryphonectria parasitica, Cryptococcus albidus, Dilophosphora alopecuri, Fusarium oxysporum, Clonostachys rosea f. catenulate (also named Gliocladium catenulatum), Gliocladium roseum, Lysobacter antibioticus, L. enzymogenes, Metschnikowia fructicola, Microdochium dimerum, Microsphaeropsis ochracea, Muscodor albus, PaeniBacillus polymyxa, Pantoea vagans, Penicilllora bilapsisomonas . giant, Picilllora bilapsisomonas. flocculosa, Pichia anomala, Pythium oligandrum, Sphaerodes mycoparasitica, Streptomyces griseoviridis, S. lydicus, S. violaceusniger, Talaromyces flavus, T. asperellum, T. atroviride, T. fertile, T. gamsii, T. harmatum, T. harzianum, T polysporum, T. stromaticum, T. virens, T. viride, Typhula phacorrhiza, Ulocladium oudemansii, Verticillium dahlia, and zucchini yellow mosaic virus (avirulent strain); L.2 Biochemical pesticides with fungicidal, bactericidal, viricidal and / or vegetal defense activating activity: hairpin protein and Reynoutria sachalinensis extract; L.3 Microbial pesticides with insecticidal, acaricidal, molluscid and / or nematicidal activity: Agrobacterium radiobacter, Bacillus cereus, B. firmus, B. thuringiensis, B. thuringiensis ssp. aizawai, B. t. ssp. israelensis, B. t. ssp. galleriae, B. t. ssp. tenebrionis, Beauveria bassiana, B. brongniartii, Burkholderia spp., Chromobacterium subtsugae, Cydia pomonella granulovirus (CpGV), Cryptophlebia leucotreta granulovirus (CrleGV), Flavobacterium spp., Helicoverpa armigera nucleopolyhedrovirus of (HearNPV), Helicoverpa zea nucleopolyhedrovirus of (HzNPV) , Helicoverpa zea single capsid nucleopolyhedrovirus (HzSNPV), Heterorhabditis bacteriophora, Isaria fumosorosea, Lecanicillium longisporum, L. muscarium, Metarhizium anisopliae, Metarhizium anisopliae var. anisopliae, M. anisopliae var. acridum, Nomuraea rileyi, Paecilomyces fumosoroseus, P. lilacinus, PaeniBacillus popilliae, Pasteuria spp., P. nishizawae, P. penetrans, P. ramosa, P. thornea, P. usgae, Pseudomonas fluorescens, nucleopolyhedrovirus of Spodoptera littoralis ) Steinernema carpocapsae, S. feltiae, S. kraussei, Streptomyces galbus, and S. microflavus; L.4 Biochemical pesticides with insecticidal, acaricidal, molluscid, pheromone and / or nematicidal activity: L-carvone, citral, (E, Z) -7,9-dodecadien-1-yl acetate, ethyl formate, (E, Z ) Ethyl -2,4-decadienoate (pear ester), (Z, Z, E) -7,11,13-hexadecatrienal, heptyl butyrate, isopropyl myristate, lavender lavender, 2-methyl 1-butanol, methyl eugenol, (E, Z) -2,13-octadecadien-1-ol acetate, (E, Z) -2,13-octadecadien-1-ol, (E, Z) -3,13-octadecadien-1 -ol, R-1-octen-3-ol, pentatermanone, (E, Z, Z) -3,8,11-tetradecatrienyl acetate, (Z, E) -9,12-tetradecadien-1-yl acetate , Z-7-tetradecen-2-one, Z-9-tetradecen-1-yl acetate, Z-11-tetradecenal, Z-11-tetradecen-1-ol, Chenopodium ambrosiodes extract, Neem oil and extract of Quillai; L.5 Microbial pesticides with plant stress reduction, plant growth regulators, plant growth promoting activity and / or performance enhancement: A. lipoferum, A. irakense, A. halopraeferens, B. elkanii, B. liaoningense, B. lupini, Delftia acidovorans, Glomus intraradices, Mesorhizobium spp., Rhizobium leguminosarum bv. phaseoli, RI bv. trifolii, RI bv. viciae, R. tropici and Sinorhizobium meliloti; F Fungicides: F.I respiration inhibitors Complex III F.I1 inhibitors at the Q0 site: azoxystrobin, cumethoxystrobin, coumoxystrobin, dimexystrobin, enestroburin, phenaminstrobin, phenoxy-strobin / fluphenoxystrobin, fluoxastrobin, cresoxim-methyl, manracystrobin, picoxystrobin, methoxystrobin, methoxystrobin, pyraxystrobin, methoxystrobin pyroxystrobin, trifloxystrobin, 2- (2- (3- (2,6-dichlorophenyl) -1-methyl-allylidene-aminoxymethyl) -phenyl) -2-methoxyimino-N-methyl-acetamide, pyribencarb, triclopyricarb / chlorodincarb, famoxadone and phenamidone, methyl-N- [2 - [(1,4-dimethyl-5-phenyl-pyrazol-3-yl) oxylmethyl] phenyl] -N-methoxy-carbamate, 1- [3-chloro-2 - [[1 - (4-chlorophenyl) -1H-pyrazol-3-yl] oxymethyl] phenyl] -4-methyl-tetrazol-5-one, 1- [3-bromo-2 - [[1- (4-chlorophenyl) pyrazole- 3-yl] oxymethyl] phenyl] -4-methyl-tetrazol-5-one, 1- [2 - [[1- (4-chlorophenyl) pyrazol-3-yl] oxymethyl] -3-methyl-phenyl] -4 -methyl-tetrazol-5-one, 1- [2 - [[1- (4-chlorophenyl) pyrazol-3-yl] oxymethyl] -3-fluoro-phenyl] -4-methyl-tetrazol-5-one, 1 - [2 - [[1 - (2,4-dichlorophenyl) pyrazol-3-yl] oxymethyl] -3-fl uoro-phenyl] -4-methyl-tetrazol-5-one, 1- [2 - [[4- (4-chlorophenyl) thiazol-2-yl] oxymethyl] -3-methylphenyl] -4-methyl-tetrazole-5 -one, 1- [3-chloro-2 - [[4- (p-tolyl) thiazol-2-yl] oxymethyl] phenyl] -4-methyl-tetrazol-5-one, 1- [3-cyclopropyl-2 - [[2-methyl-4- (1-methylpyrazol-3-yl) phenoxy] methyl] phenyl] -4-methyl-tetrazol-5-one, 1- [3- (difluoromethoxy) -2 - [[2- methyl-4- (1-methylpyrazol-3-yl) phenoxy] methyl] phenyl] -4-methyl-tetrazol-5-one, 1-methyl-4- [3-methyl-2 - [[2-methyl-4 - (1-methylpyrazol-3-yl) phenoxy] methyl] phenyl] tetrazol-5-one, 1-methyl-4- [3-methyl-2 - [[1- [3- (trifluoromethyl) phenyl] -ethylideneamino] oxymethyl] phenyl] tetrazol-5-one, (Z, 2E) -5- [1- (2,4-dichlorophenyl) pyrazol-3-yl] oxy-2-methoxyimino-N, 3-dimethyl-pent-3- enamide, (Z, 2E) -5- [1- (4-chlorophenyl) pyrazol-3-yl] oxy-2-methoxyimino-N, 3-dimethyl-pent-3-enamide and (Z, 2E) -5- [1- (4-chloro-2-fluoro-phenyl) pyrazol-3-yl] oxy-2-methoxyimino-N, 3-dimethyl-pent-3-enamide; F.12 Complex III inhibitors at the Qi site: cyazofamide, amisulbrom, 2-methylpropanoate [(3S, 6S, 7R, 8R) -8-benzyl-3 - [(3-acetoxy-4-methoxy-pyridine-2 -carbonyl) amino] -6-methyl-4,9-dioxo-1,5-dioxonan-7-yl], [(3S, 6S, 7R, 8R) -8-benzyl-3 - [[ 3- (acetoxymethoxy) -4-methoxy-pyridine-2-carbonyl] amino] -6-methyl-4,9-dioxo-1,5-dioxonan-7-yl], 2-methylpropanoate [(3S, 6S, 7R, 8R) -8-benzyl-3 - [(3-isobutoxycarbonyloxy-4-methoxy-pyridine-2-carbonyl) amino] -6-methyl-4,9-dioxo-1,5-dioxonan-7-yl] , [(3S, 6S, 7R, 8R) -8-benzyl-3 - [[3- (1,3-benzodioxol-5-ylmethoxy) -4-methoxy-pyridine-2-carbonyl] amino], 2-methylpropanoate -6-methyl-4,9-dioxo-1,5-dioxonan-7-yl]; (3S, 6S, 7R, 8R) -3 - [[(3-hydroxy-4-methoxy-2-pyridinyl) carbonyl] amino] -6-methyl-4,9-dioxo-8- (phenylmethyl ) -1,5-dioxonan-7-yl and (3S, 6S, 7R, 8R) -8-benzyl-3- [3 - [(isobutyryloxy) methoxy] -4-methoxypicolinamido] -6-methyl-4 isobutyrate , 9-dioxo-1,5-dioxonan-7-yl; F.I3 Complex II inhibitors: pidiflumetofen, benodanyl, benzovindiflupir, bixafen, boscalid, carboxin, fenfuram, fluopyram, flutolanil, fluxapyroxad, furametpyr, isofetamid, isopyrazam, mepronil, oxycarboxin, silk, petalamio-pyrophlufenoid, petalamio-pyrophlufenoid (4'-trifluoromethylthiobiphenyl-2-yl) -3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxamide, N- (2- (1,3,3-trimethyl-butyl) -phenyl) -1,3 -dimethyl-5-fluoro-1H-pyrazole-4-carboxamide, 3- (difluoromethyl) -1-methyl-N- (1,1,3-trimethylindan-4-yl) pyrazole-4-carboxamide, 3- (trifluoromethyl ) -1-methyl-N- (1,1,3-trimethylindan-4-yl) pyrazole-4-carboxamide, 1,3-dimethyl-N- (1,1,3-trimethylindan-4-yl) pyrazole- 4-carboxamide, 3- (trifluoromethyl) -1,5-dimethyl-N- (1,1,3-trimethylindan-4-yl) pyrazole-4-carboxamide, 1,3,5-trimethyl-N- (1,1,3- trimethylindan-4-yl) pyrazole-4-carboxamide, N- (7-fluoro-1,1,3-trimethyl-indan-4-yl) -1,3-dimethyl-pyrazole-4-carboxamide and N- [2 - (2,4-dichlorophenyl) -2-methoxy-1-methyl-ethyl] -3- (difluoromethyl) -1-methyl-pyrazole-4-carboxamide; F.I4 Other respiration inhibitors: Diflumethorim, (5,8-difluoroquinazolin-4-yl) - {2- [2-fluoro-4- (4-trifluoromethylpyridin-2-yloxy) -phenyl] -ethyl} -amine ; nitrophenyl derivatives: binapacryl, dinobuton, dinocap, fluazinam, ferimzone; organometallic compounds: fenthin acetate, fenthin chloride, and fenthin hydroxide; Amethoctradine; and silthofam; F.II Inhibitors of sterol biosynthesis: F.II1 Demethylase C14 inhibitors: triazoles: azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, mefentrifluconazole, propconautconazole, peniconabiconazole, micropconazole, penicconazole, microponaconazole, micronazole simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole, uniconazole. 1- [rel- (2S; 3R) -3- (2-chlorophenyl) -2- (2,4-difluorophenyl) -oxyranylmethyl] -5-thiocyanate-1H- [1,2,4] triazolo, 2- [ rel- (2S; 3R) -3- (2-chlorophenyl) -2- (2,4-difluorophenyl) -oxyranylmethyl] -2H- [1,2,4] triazole-3-thiol, 2- [2-chloro -4- (4-chlorophenoxy) phenyl] -1- (1,2,4-triazol-1-yl) 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-triazole -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-1-yl) butan-2-ol, 2- [4- (4 -chlorophenoxy) -2- (trifluoromethyl) phenyl] -1- (1,2,4-triazol-1-yl) propan-2-ol, 2- [2-chloro-4- (4-chlorophenoxy) phenyl] - 3-methyl-1- (1,2,4-triazol-1-yl) butan-2-ol, 2- [4- (4-chlorophenoxy) -2- (trifluoromethyl) phenyl] -1- (1,2 , 4-triazol-1-yl) pentan-2-ol, 2- [4- (4-fluorophenoxy) -2- (trifluoromethyl) phenyl] -1- (1,2,4-triazol-1-yl) propan -2-ol, 2- [2-chloro-4- (4-chlorophenoxy) phenyl] -1- (1,2,4-triazol-1-yl) pent-3-in-2-ol; imidazoles: imazalil, pefurazoate, prochloraz, triflumizole; pyrimidines, pyridines, and piperazines: fenarimol, nuarimol, pyrifenox, triforine, and [3- (4-chloro-2-fluoro-phenyl) -5- (2,4-difluorophenyl) isoxazol-4-yl] - (3-pyridyl) methanol; F.II2 Delta14-reductase inhibitors: aldimorf, dodemorf, dodemorf acetate, fenpropimorph, tridemorph, fenpropidine, piperaline, and spiroxamine; F.II3 3-keto reductase inhibitors: fenhexamide; F.III Inhibitors of nucleic acid synthesis F.IM1 phenylamides or acylamino acid fungicides: benalaxyl, benalaxyl-M, kiralaxil, metalaxyl, metalaxyl-M (mephenoxam), ofurace and oxadixyl; F.III2 others: hymexazole, octilinone, oxolinic acid, bupyrimate, 5-fluorocytosine, 5-fluoro-2- (p-tolylmethoxy) pyrimidin-4-amine and 5-fluoro-2- (4-fluorophenyl-methoxy) pyrimidine- 4-amine; F.IV Inhibitors of cell division and the cytoskeleton. F.IV1 Tubulin inhibitors of the benzimidazole and thiophanate class: benomyl, carbendazim, fuberidazole, thiabendazole and thiophanate-methyl; triazolopyrimidines: 5-chloro-7- (4-methylpiperidin-1-yl) -6- (2,4,6-trifluoro-phenyl) - [1,2,4] triazolo [1,5-a] pyrimidine; Y F.IV2 other inhibitors of cell division: dietofencarb, etaboxam, pencycuron, fluopicolide, zoxamide, metrafenone, pyrophenone; F.V Amino Acid and Protein Synthesis Inhibitors: F.V1 Inhibitors of methionine synthesis of the class of anilino-pyrimidines: cyprodinil, mepanipyrim and pyrimethanil; and F.V2 Protein synthesis inhibitors: blasticidin-S, kasugamycin, kasugamycin hydrochloride-hydrate, mildiomycin, streptomycin, oxytetracycline, polyoxin, and validamycin A; F.VI Inhibitors of signal transduction: F.VI1 MAP / histidine kinase inhibitors: fluoroimide, iprodione, procymidone, vinclozolin, fenpiclonil and fludioxonil; Y F.VI2 G protein inhibitors: quinoxyfen; F.VII Inhibitors of lipid and membrane synthesis: F.VII1 Inhibitors of phospholipid biosynthesis: edifenfos, iprobenfos, pyrazofos, isoprothiolane; F.VII2 lipid peroxidation: dichloran, quintacene, technazene, tolclofos-methyl, biphenyl, chloroneb, and etridiazole; F.VII3 Phospholipid biosynthesis and cell wall deposition: dimethomorph, flumorf, mandipropamid, pirimorf, benthiavalicarb, iprovalicarb, valifenalate and (4-fluorophenyl) acid ester N- (1- (1- (4-cyano-phenyl) ethanesulfonyl) -but-2-yl) carbamic; F.VII4 compounds that affect the permeability of the cell membrane and fatty acids: propamocarb; and F.VII5 Fatty acid amide hydrolase inhibitors: oxathiapiproline, 2- {3- [2- (1 - {[3,5-bis (difluoromethyl-1H-pyrazol-1-yl) acetyl} piperidin-4- yl) -1, 3-thiazol-4-yl] -4,5-dihydro-1,2-oxazol-5-yl} phenyl methanesulfonate, 2- {3- [2- (1 - {[3,5 -bis (difluoromethyl) -1H-pyrazol-1-yl] acetyl} piperidin-4-yl) and 1,3-thiazol-4-yl] -4,5-dihydro-1,2-oxazol-5- methanesulfonate yl} -3-chlorophenyl; F.VIII Inhibitors with multisite action: F.VIII1 inorganic active substances: Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate and sulfur; F.VIII2 thio and dithiocarbamates: ferbam, mancozeb, maneb, metam, metiram, propineb, thiram, zineb and ziram; F.VIII3 organochlorine compounds of the class of phthalimides, sulfa drugs and chloronitriles: anilazine, chlorothalonil, captafol, captan, folpet, dichlorofluanide, dichlorophene, hexachlorobenzene, pentachlorophenols and their salts, phthalide, tolylfluanid and N- (4-chloro -phenyl) -N-ethyl-4-methyl-benzenesulfonamide; Y F.VIII4 guanidines and others: guanidine, dodyne, dodyne free base, guazatine, guazatine acetate, iminoctadin, iminoctadin-triacetate, iminoctadin-tris (albesylate), dithianon and 2,6-dimethyl-1H, 5H- [1, 4] dithiino [2,3-c: 5,6-c '] dipyrrole-1,3,5,7 (2H, 6H) -tetraone; F.IX Inhibitors of cell wall synthesis: F.IX1 glucan synthesis inhibitors: validamycin and polyoxin B; F.IX2 melanin synthesis inhibitors: pyoquilon, tricyclazole, carpropamid, dicyclomet and phenoxanil; F.X Plant defense inducers: F.X1 acibenzolar-S-methyl, probenazole, isothianyl, thiadinyl, prohexadione-calcium; F.X2 Phosphonates: Phosethyl, Phosetylaluminum, Phosphorous Acid and their salts; potassium or sodium bicarbonate; Y F.XI Unknown mode of action: bronopol, quinomethionate, cyflufenamide, cymoxanil, dazomet, debacarb, diclomezine, diphenzoquat, diphenzoquatmethylsulfate, diphenylamine, phenpyrazamine, flumethover, flusulfamide, flutianil, metasulfocarb, nitrapyrin, nitrothalidine-isopropylpropyl, oxoxylamine-proquinolipropyl triazoxide, 2-butoxy-6-iodo-3-propylchrome-4-one, 2- [3,5-bis (difluoromethyl) -1H-pyrazol-1-yl] -1 - [4- (4- {5- [2- (prop-2-yn-1 -yloxy) phenyl] -4,5-dihydro-1,2-oxazol-3-yl} -1,3-thiazol-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-in-1 -yloxy) phenyl] -4,5-dihydro-1,2-oxazol-3-yl} -1,3-thiazol-2-yl) piperidin-1-yl] ethanone, 2- [3,5-bis ( difluoromethyl) -1H-pyrazol-1-yl] -1- [4- (4- {5- [2-chloro-6- (prop-2-y-1-yloxy) phenyl] -4,5-dihydro- 1,2-oxazol-3-yl} -1,3-thiazol-2-yl) piperidin-1-yl] ethanone, N- (cyclopropylmethoxyimino- (6-difluoro-methoxy-2,3-difluoro-phenyl) - methyl) -2-phenyl acetamide, N '- (4- (4-chloro-3-trifluoro-methylphenoxy) -2,5-dimethyl-phenyl) -N -ethyl-N-methylformamidine, N '- (4- (4-fluoro-3-trifluoromethyl-phenoxy) -2,5-dimethyl-phenyl) -N-ethyl-N-methylformamidine, N' - (2-methyl- 5-trifluoromethyl-4- (3-trimethylsilanyl-propoxy) -phenyl) -N-ethyl-N-methylformamidine, N '- (5-difluoromethyl-2-methyl-4- (3-tri-methylsilanyl-propoxy) -phenyl ) -N-ethyl-N-methylformamidine, 6-tert-butyl-8-fluoro-2,3-dimethyl quinolin-4-yl methoxy-acetic acid ester, 3- [5- (4-methylphenyl) -2,3-dimethyl-isoxazolidin-3-yl] -pyridine, 3- [5- (4-chlorophenyl) -2,3-dimethyl-isoxazolidin-3-yl] -pyridine (pyrisoxazole), cyclopropanecarboxylic acid N- (6-methoxy-pyridin-3-yl) amide, 5-chloro-1- (4,6-dimethoxy-pyrimidin-2-yl) -2-methyl-1H-benzoimidazole, 2- (4-chloro-phenyl) -N- [4- (3,4-dimethoxy- phenyl) -isoxazol-5-yl] -2-prop-2-ynyloxy-acetamide, ethyl (Z) -3-amino-2-cyano-3-phenyl-prop-2-enoate, picarbutrazox, N- [6 Pentyl - [[(Z) - [(1-methyltetrazol-5-yl) -phenyl-methylene] amino] oxymethyl] -2-pyridyl] carbamate, 2- [2 - [(7,8-difluoro-2- methyl-3-quinolyl) oxy] -6-fluoro-phenyl] propan-2-ol, 2- [2-fluoro-6 - [(8-fluoro-2-methyl-3-quinolyl) oxy] phenyl] propan- 2-ol, 3- (5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl) quinoline, 3- (4,4-difluoro-3,3-dimethyl-3, 4-dihydroisoquinolin-1-yl) quinoline, 3- (4,4,5-trifluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl) quinoline, and 9-fluoro-2,2-dimethyl- 5- (3-quinolyl) -3H-I, 4-ben zoxazepine. The pesticidal mixtures according to claim 3, wherein component C is selected from the group consisting of cyclaniliprole, carbofuran, oxamyl, thiodicarb, fipronil, bifenthrin, cyfluthrin, beta-cyfluthrin, alphacypermethrin, tefluthrin, acetamiprid, clothianidin, imidacloprid, thiacloprid, thiamethoxam, abamectin, chlorantraniliprole, cyanthraniliprole, tetranyliprole, broflanilide, sulfoxaflor, thioxazafen, triflumezopyrim, and the Bacillus thuringiensis proteins Cry1Ab, Cry1Ac, Cry3Ab3, Cry1b, Cry1Ac, Cry3Ab3, Cry1b3, CrybB3 and Cry1Ac, Cry3Ab3, The pesticidal mixtures according to claim 3, wherein component C is selected from the group consisting of Bacillus firmus, Pasteuria nishizawae, Pasteuria penetrans, Rhizobium leguminosarum bv. phaseoli, Rhizobium leguminosarum bv. trifolii, Rhizobium leguminosarum bv. viciae, Burkholderia spp. and Rhizobium tropici. 6. The pesticidal mixtures according to claim 3, wherein component C is selected from the group consisting of azoxystrobin, pyractrostrobin, trifloxystrobin, fluopyram, fluxapyroxad, penflufen, sedaxane, fluazinam, difenoconazole, ipconazole, prothioconazole, tebuconazole, metalaxyl, triticone, metalaxyl-M (mephenoxam), mefentrifluconazole, thiabendazole, fludioxonil, benzovindiflupir, picarbutrazox, etaboxam, pidiflumetofen, fenpicoxamide, thiophanate-methyl, myclobutanil, and oxathiapiproline. The pesticidal mixtures according to any one of claims 3 to 6, comprising at least two C components. The pesticidal mixtures according to claim 7, comprising at least two C components selected from the group consisting of thiamethoxam, ciazipir, rinaxypyr, fludioxonil, metalaxyl-M (mephenoxam), mefentrifluconazole, azoxystrobin, pyraclostrobin, fluxapiroxad, thiabendazole clothianidin, prothioconazole, penflufen, metalaxyl, and imidacloprid. 9. Method for controlling pests, which method comprises applying the pesticide mixtures, as defined in any one of claims 1 to 8, to plants, plant propagation material or the place of growth of the plants; pests or their food supply, habitat or breeding grounds, excluding methods for treating the human or animal body by surgery or therapy. 10. The method according to claim 9, wherein the pests are nematodes. II. The method according to claim 10, wherein the nematodes are selected from the group consisting of Meloidogyne spp., Heterodera spp., Pratylenchus spp., Longidorus spp., Belonolaimus spp. and Globodera spp. 12. The methods according to any one of claims 9 to 11, wherein the pesticidal mixture as defined in any one of claims 1 to 8 is applied to the plant propagation material. The method according to any one of claims 9 to 12, wherein the pesticidal mixture as defined in any one of claims 1 to 8 is applied to plants or their propagating material selected from the group consisting of agricultural plants, forestry and horticultural crops, each in its natural or genetically modified form. The method according to any one of claims 9 to 13, wherein the mixture of pesticides as defined in any one of claims 1 to 8 is applied simultaneously, that is to say jointly or separately, or in succession . 15. An agrochemical composition, comprising at least one auxiliary and a mixture as defined in any one of claims 1 to 8. 16. Plant propagation material comprising a pesticidal mixture as defined in any one of claims 1 to 8 or an agrochemical composition as defined in claim 15.