(JP2018027958) 1. In the composition, of at least 1 kinds of biological pesticide ' here, the biological pesticide is, bacillus, accession number kichinosuporusu B-21618 (Bacillus chitinosporus) AQ746(NRRL), bacillus, YCpMmycl B-21664 (Bacillus myc oides) AQ726(NRRL Accession), bacillus, pumilus B-30087 (B acillus pumilus) (NRRL Accession), bacillus, 62 pumilus B-216 (Bacillus pumilus) AQ717(NRRL Accession), accession number 55 608 bacillus (Bacillus sp.) AQ175(ATCC spp), accession number 5 5609 bacillus (Bacillus sp.) AQ177(ATCC spp), accession number 53522 bacillus (Bacillus sp.) AQ178(ATCC spp), bacillus, subtilis accession number B-21665 (Bacillus subtilis) AQ74 3(NRRL), bacillus, subtilis accession number B-21661 (Bacillus s ubtilis) AQ713(NRRL), bacillus, 55614 accession number (Bacillus subtilis) AQ153(ATCC subtilis), bacillus, (Bacillus thuringiensis) BD #32 (NRRL Accession B-21530) thuringiensis, bacillus, thuringiensis B-21619 (Bacil lus thuringiensis) AQ52(NRRL Accession), muscodor, arbus (Muscodor albus) 620(NRRL Accession No. HB 30 547), muscodor, roseus (Muscodor roseus) A3-5(NRR L Accession No. HB 30548), rodokokkusu, accession number guroberurusu B-21663 (Rhodococcus gl oberulus) AQ719(NRRL), Marinomyces, 30232 accession number garubusu (Streptomyces galbus) (NRRL), Marinomyces B-30145 Accession (Streptomyces sp.) (NRRL spp), bacillus, thuringiensis, subgenuses, bacillus (Bacillus thuringiensis subspec.kurstaki) BMP123, taki Cruz, b-50421 (Bacillus subtilis) AQ30002(NRRL subtilis accession number) and bacillus, subtilis accession number B-50455 (Bacillus subtili s) AQ30004(NRRL), and/or, each of said microorganisms have all of the identifying characteristics of strain stock mutant, and/or, insects, mites, nematodes and/or to a plant pathogen activity produced by said microbial metabolites are individual selected from the group consisting 'of 1 and at least two arylaminotriazoles' where, the insecticide, voltage-dependent sodium channel modulators and the sodium channel blocker is selected from the group consisting of' in an amount effective to synergistically DMA_ADR, composition. 2. Wherein the sodium channel modulators/voltage-dependent sodium channel blocker and a therapeutic agent or, pyrethroid, DDT, methoxychlor, indoxacarb and metaflumizone is selected from the group consisting of, a composition according to claim 1. 3. Wherein the sodium channel modulators/voltage-dependent sodium channel blockers and or the, group consisting of, allethrin, d- cis-transformer ares phosphorus, d- transformer ares phosphorus, acrinathrin, bioallethrin, bioallethrin S- cyclopentenyl isomer, bioresmethrin, bifenthrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin [(1R) -trans isomers], deltamethrin, empenthrin [(EZ) -isomers (1R) ], esfenvalerate, etofenprox, fenpropathrin, cypermethrin, fenvalerate, flumethrin, tau-esfenvalerate, halfenprox, imiprothrin, kadethrin, permethrin, phenothrin [(1R) -trans isomers], prallethrin, pyrethrin (pyrethrum (pyre thrum)), resmethrin, silafluofen, tefluthrin, tetramethrin, tetramethrin [(1R) isomer], tralomethrin, transfluthrin, DDT, methoxychlor, indoxacarb and metaflumizone is selected from the group consisting of, the composition according to claim 2. 4. Wherein the voltage-dependent sodium channel modulators and the sodium channel blocker, a group, alpha-cypermethrin, beta-cyfluthrin, acrinathrin, cyfluthrin, cypermethrin, deltamethrin, gamma-cyhalothrin, lambda-cyhalothrin, tefluthrin, indoxacarb and metaflumizone is selected from the group consisting of, a composition according to claim 3. 5. 1 At least two types of the sanitizing agent further comprises (however, the biological pesticide and a fungicide is, not the same), composition according to any one of claims 1-4. 6. Wherein the sterilizing agent, is selected from the group consisting of the following, the composition of claim any one of claims 1-5: an inhibitor of ergosterol biosynthesis, inhibitors of the respiratory chain complex II or in I agents, inhibitors of the respiratory chain at complex I II, inhibitors of the mitosis and cell division, a compound capable of inducing a host defense, amino acids and/or protein biosynthesis inhibitor, an inhibitor of ATP production, cell wall synthesis inhibitors, lipid and membrane synthesis inhibitors, inhibitors of the melanine biosynthesis, for nucleic acid synthesis inhibitor, signal transduction inhibitors, compounds that can act as an uncoupling agent, for example, binapacryl, dinocap, ferimzone, An, main heptyl gino cup, and, further compounds, for example, bench azole, betokisajin, kapushimaishin (capsimycin), carboxylic, kinomechioneto, piriofenon ((chlazafen one) kurazafenon), kufuranebu, cyflufenamid, cymoxanil, cyprosulfamide, dazomet, debakarubu, dichlorophen, jikuromejin, jifenzokoto, di fen zone court methyl sulfate, diphenylamine, ekomeito, fenpyrazamine, furumetoberu, furuoruimido, flusulfamide, furuchianiru, fosetyl-aluminium, fosetyl-calcium, fosetyl-sodium, hexachlorobenzene, irma clarithromycin, methasulfocarb, methyl isothiocyanate, metrafenone, mildiomycin, natamycin, nickel dimethyldithiocarbamate, nitorotaru-isopropyl, okuchirinon, okisamokarubu (oxamocarb), oxyphene ji inn (oxyfenthii n), pentachlorophenol and salt, dphenothrin, phosphorous acid and its salts, propamocarb-(propamocarb-fosetylate), hosechireto puropanoshin-sodium purokinajido (propanosine-sodium), pirimorufu, -3 - (2E) -3 - (4-tert - butylphenyl) (2-- chloropyridin -4 - yl) -2 - -1 - -1 - (-4 - morpholin yl) enqueued propynyls ON, -3 - (2Z) -3 - (4-tert - butylphenyl) (2-- chloropyridin -4 - yl) -2 - -1 - -1 - (-4 - morpholin yl) on enqueued propynyls, pyrrolnitrin, tebufurokin, tecloftalam, torunifanido, triazoxide, torikuramido, , -8 - (3S, 6 S, 7R, 8R) -3 - benzyl [( {3-[(isobutyryloxy) methoxy] -2 - - methoxypyridin - -4 - - yl} carbonyl) amino] -4,9 - - methyl - -7 - - yl jiokisonan -1,5 - dioxo -6-2-methylpropanoate, 1-(4-{4-[(5R) -5 - (2,6 - - difluorophenyl) -4,5 - - dihydro - -1,2 - - oxazol -3 - - yl] thiazol - -2 - yl -1,3 -} piperidine - -1 - - yl) -2 - [5--1H - -3 - -1 - (trifluoromethyl) pyrazol-l-yl-methyl] ethanone, 1-(4-{4-[(5S) -5 - (2,6 - - difluorophenyl) -4,5 - - dihydro - -1,2 - - oxazol -3 - - yl] thiazol - -2 - yl -1,3 -} piperidine - -1 - - yl) -2 - [5-- methyl - -1 --pyrazol - -3 - (trifluoromethyl) -1H --l-yl] ethanone, 1-(4-{4-[5-(2,6 - - difluorophenyl) -4,5 - - dihydro - -1,2 - - oxazol -3 - - yl] thiazol - -2 - yl -1,3 -} piperidine - -1 - - yl) -2 - [5-- methyl - -1 --pyrazol - -3 - (trifluoromethyl) -1H --l-yl] ethanone, 1-- yl (4-- methoxyphenoxy) -1 - -3,3-1H - -2 - dimethylbutane melt.These imidazole, (methylsulfonyl) pyridin - -4 - tetrachloroammoniumplatinate 2, 3, 5, 6 -, dibutyl -6 - chlorothieno 2, 3-d 2,3 -: -4 (3H) a pyrimidine-ON, -1H dimethyl 2,6 -, 5H - [1, 4] dithiino [2, 3-c: 5, 6-c '] dipyrrole (2H, 6H) - 1, 3, 5, 7-Tetron, 2-[5-(trifluoromethyl) pyrazol - -1 - - yl -3 - - methyl - -1H -] -1 - (4-{4-[(5R) -5 - - phenyl - -4,5 - - dihydro - -1,2 - - oxazol -3 - - yl] thiazol - -2 - yl -1,3 -} piperidine - -1 - - yl) ethanone, 2-[5-(trifluoromethyl) -1 --pyrazol - -3 - - yl methyl - -1H -] -1 - (4-{4-[(5S) -5 - - phenyl - -4,5 - - dihydro - -1,2 - - oxazol -3 - - yl] thiazol - -2 - yl -1,3 -} piperidine - -1 - - yl) ethanone, 2-[5-(trifluoromethyl) -1 --pyrazol - -3 - - yl methyl - -1H -] -1 - {4-[4-(5-- phenyl - -1 - dihydro - -4,5 -, 2--3 - Oxazole-l-yl) thiazol - -2 - yl -1,3 -] piperidin - -1 - - yl} ethanone, 2-- butoxy - -4 --chromen -6 - ON -3 - iodo -4H - propyl, 2-- chloro - -5 - [2-- chloro - -1 - (2,6 - - difluoro - -4 - - methoxyphenyl) -1H - - methyl - -5 --imidazole -4 - - yl] pyridine, 2--phenylphenol and salts, 3-( -3,4 - dimethyl -1 - dihydroisoquinoline Guardpak 4, 4, 5 - -3,3 - - yl) Zquinolone, -2,6 - - dicarbonitrile trichloropyridine^ 3, 4, 5 -, 3-[5-(4-- chlorophenyl) oxazolidin - -2,3 - - yl -1,2 - - dimethyl - -3 -] pyridine, 3-chloro -4 - (4-- chlorophenyl) (2,6 - - difluorophenyl) -5 - -6 - methylpyridazin, 4--3,6 - -5 - (2,6 - - difluorophenyl) (4-- chlorophenyl) dimethyl pyridazine, 5-- thiadiazol - -2 - - 1, 3, 4 - amino thiol, 5-- chloro -N '- phenyl - N' - (-1 --prop - -2 - - yl) thiophene - -2 - sulfonohydrazide, 5-[(4-- fluorobenzyl) oxy] pyrimidin - -2 - - fluoro -4 - amine, 5-[(4-- methylbenzyl) oxy] pyrimidin - -2 - - fluoro -4 - amine, 5--6 - methyl octyl 1, 2, 4: triazolo 1, 5-a: -7 - pyrimidine amine, phenylpropanolamine (2Z) -2 - -3 - -3 - -2 - amino ethyl ene cyano, N' - (4-{[3-(4-- chlorobenzyl) - 1, 2, 4 - -5 - - yl ring and a thiadiazole] oxy} -2,5 - - dimethylphenyl) -N- methyl imide formamide -N- ethyl, -3 - (4-- chlorobenzyl) N- [3-- methoxy - -4 - (-1 --prop - -2 - - yloxy) phenyl] propanamide, N- [(4-- chlorophenyl) (cyano) methyl] -3 - [3-- methoxy - -4 - (-1 --prop - -2 - - yloxy) phenyl] propanamide, N- [(5-- bromo - -2 - - yl -3 - chloropyridin) methyl] -3 - dichloropyridine - -2,4 - - carboxamide, N- [1-(5-- bromo - -2 - - yl -3 - chloropyridin) ethyl] carboxamide -2,4 - -3 - dichloropyridine, N- [1-(5-- bromo - -2 - - yl -3 - chloropyridin) ethyl] -2 - - fluoro - -3 - carboxamide -4 - iodopyridine, n - {(E) -[(cyclopropylmethoxy) imino] methyl [6-(difluoromethoxy) -2,3 - difluorophenyl]} -2 - phenyIacetamide, N- {(Z) -[(cyclopropylmethoxy) imino] methyl [6-(difluoromethoxy) -2,3 - difluorophenyl]} -2 - phenyIacetamide, N'- {4-[(3-tert - butyl -4 - - cyano - -1,2 --thiazol - -5 - - yl) oxy] phenyl -5 - - chloro - -2 -} methyl imide formamide -N- ethyl -N -, methyl N- -2 - (1-{[5-- methyl - -3 - (trifluoromethyl) -1H --pyrazol - -1 - - yl] acetyl} piperidin - -4 - - yl) thiazol - -1,3 - -N- -4 - (-1 - tetrahydronaphalene 1, 2, 3, 4 - yl) carboxamide, methyl -2 -N- (1-{[5-- methyl - -3 - (trifluoromethyl) -1H --pyrazol - -1 - - yl] acetyl} piperidin - -4 - - yl) -N- -1,3 - [-1 - (1R) yl - 1, 2, 3, 4 - tetrahydronaphalene] thiazole -4 - - carboxamide, -2 - - methyl N- (1-{[5-- methyl - -3 - (trifluoromethyl) -1H --pyrazol - -1 - - yl] acetyl} piperidin - -4 - - yl) -N- -1,3 - [-1 - (1S) yl - 1, 2, 3, 4 - tetrahydronaphalene] thiazole -4 - - carboxamide, {6-[ ({[ (1-- methyl - -1H --tetrazol - -5 - - yl) (phenyl) methylidene] amino} oxy) methyl] pyridin - -2 - - yl} - carbamic acid pentyl, phenazine-l-carboxylic acid -1 -, -8 - qiiiiioliis DRZQIP, all sulfates (2:1) quinoline -8 -, {6-[ ({[ (1-- methyl - -1H --tetrazol - -5 - - yl) (phenyl) methylene] amino} oxy) methyl] pyridin - -2 - - yl} carbamic acid tert - butyl, 1-- N- -3 - (trifluoromethyl) methyl [2' - (trifluoromethyl) biphenyl - -2 - - yl] -4 --pyrazol - -1H - - carboxamide, -3 - (4 '- chlorobiphenyl -2 - yl) N- (difluoromethyl) -4 --pyrazol - -1 - - carboxamide methyl -1H -, N- (2', 4' - dichlorobiphenyl -2 - yl) methyl - -4 --pyrazole -1 - -3 - -1H - (difluoromethyl) - carboxamide, 3-(Difluoromethyl) -N- -1 - - methyl [4 '- (trifluoromethyl) biphenyl - -2 - - yl] -1H --pyrazole - -4 - carboxamide, N- (2', 5 '- difluorobiphenyl-l -2 -) -1H - -1 - -4 - -3 - methyl (trifluoromethyl) pyrazole carboxamide, 3-- N- -1 - (difluoromethyl) methyl [4' - (-1 --prop - -1 - - yl) biphenyl - -2 - - yl] -1H --pyrazole - -4 - carboxamide, 5-- dimethyl -N- -1,3 --fluoro [4 '- (-1 --prop - -1 - - yl) biphenyl - -2 - - yl] -4 --pyrazole - -1H - - carboxamide, 2-- N- chloro [4' - (-1 --prop - -1 - - yl) biphenyl - -2 - - yl] pyridine - -3 - carboxamide, 3-- N- (difluoromethyl) [4 '- (3,3 - - dimethylbut-l-yl--1 ---1 -) biphenyl -2 - - yl] pyrazol - -1H - - methyl - -4 - - carboxamide -1 -, N- [4' - (3,3 - - dimethylbut-l-yl--1 ---1 -) biphenyl -2 - - yl] pyrazol - -1,3 - - fluoro - -4 - carboxamide -1H - dimethyl -5 -, 3-(difluoromethyl) -1 - -N- -1H - (4 '- ethynylbiphenyl -2 - yl) methyl - -4 --pyrazol carboxamide, fluoro (4' - -2 - - yl ethynylbiphenyl) N- -5 --pyrazol - -1,3 - dimethyl - -4 - - carboxamide -1H -, 2-- chloro-pyridin -N- -3 - (4 '- ethynylbiphenyl -2 - yl) carboxamide, 2-- N- chloro [4' - (3,3 - - dimethylbut-l-yl--1 ---1 -) - biphenyl - -2 - - yl] pyridine - -3 - carboxamide, 4-- N- -2 - (difluoromethyl) methyl [4 '- (trifluoromethyl) biphenyl - -2 - - yl] thiazol - -5 - - carboxamide -1,3 -, 5-- N- fluoro [4' - (3-- hydroxy - -3 - - yl--1 ---1 - methylbut) biphenyl - -2 - - yl] -4 --pyrazol - -1,3 - - dimethyl - -1H - - carboxamide, 2-- N- chloro [4 '- (3-- hydroxy - -3 - - yl--1 ---1 - methylbut) biphenyl - -2 - - yl] pyridine - -3 - carboxamide, 3-- N- (difluoromethyl) [4' - (3-- methoxy - -3 - - yl--1 ---1 - methylbut) biphenyl - -2 - - yl] methyl - -4 --pyrazol - -1 - - carboxamide -1H -, 5-- N- fluoro [4' - (3-- methoxy - -3 - - yl--1 ---1 - methylbut) biphenyl - -2 - - yl] -1, 3-Dimethyl - -4 --pyrazol - -1H - - carboxamide, 2-- N- chloro [4' - (3-- methoxy - -3 - - yl--1 ---1 - methylbut) biphenyl - -2 - - yl] pyridine - -3 - - carboxamide, (5-- bromo - -3 - - yl -4 - - methoxy - -2 - - methylpyridin) methanone (-6 - - methylphenyl 2, 3, 4 - trimethoxy), N- [2-(4-{[3-(4-- chlorophenyl) prop - -2 ---1 --yl] oxy} -3 - - methoxyphenyl) ethyl] (methylsulfonyl) valinamide - N2 -, 4-- oxo - -4 - [(2-- phenylethyl) amino] butanoic acid, -1 - - yl--3 --porcine {6-[ ({[ (Z) -(1-- methyl - -1H --tetrazol - -5 - - yl) (phenyl) methylene] amino} oxy) methyl] pyridin - -2 - - yl} carbamate, 4--5 - -2 - fluoro pyrimidine amino polyols, propyl 3, 4, 5 - trihydroxy benzoic acid, and, orysastrobin. 7. Wherein the biological control agent, selected from the group consisting of the following, composition according to any one of claims 1-6: bacillus, 087 pumilus B-30 (Bacillus pumilus) (NRRL Accession), bacillus, subtilis accession number B-50421 (Bacillus subtilis) AQ3000 2(NRRL) and bacillus, subtilis accession number B-21661 (Bacillus subtilis) AQ713(NRRL), and/or, each of said microorganisms have all of the identifying characteristics of a strain of the mutant stock, and/or, insects, mites, and/or nematodes as the above microorganism is a plant pathogen which shows activity on metabolites produced by strains of the individual. 8. Bulking agents, solvents, carrier spontaneous (spontaneity promoter), enhancer, an emulsifier, dispersant, (frost protectant) antifreeze agent, a thickening agent and at least one selected from the group consisting of an adjuvant 1 further comprising auxiliary agents, the composition of any one of claims 1-7. 9. In any one of claims 1-8 composition to the treated seed. 10. Wherein the concentration of the insecticide composition, selected from the group consisting of the cypermethrin and tefluthrin, according to claim 9 seeds. 11. As a bactericide or insecticide and/of, any one of claims 1-8 comprises the use of the composition. 12. The insects, mites, nematodes and/or caused by a plant pathogen of the plant and the plant parts are harvested whole fruits or vegetables as well as damage in order to decrease the loss of, the use according to claim 11. 13. The insects, mites, nematodes and/or plant pathogens caused by damage to the plants and plant parts as well as to the overall loss in harvested fruits or vegetables in a method to reduce, at least 1 kinds of biological pesticide ' here, the biological pesticide is, bacillus, 18 accession number kichinosuporusu B-216 (Ba cillus chitinosporus) AQ746(NRRL), bacillus, YCpMmycl B-21664 (Bacillus mycoides) AQ726(N RRL Accession), bacillus, pumilus B-30087 (Bacillus pumil us) (NRRL Accession), bacillus, pumilus B-21662 (Bacillus pumilus) AQ717(NRRL Accession), accession number 55608 bacillus (Ba cillus sp.) AQ175(ATCC spp), accession number 55609 bacillus (B acillus sp.) AQ177(ATCC spp), accession number 53522 bacillus (Bacillus sp.) AQ178(ATCC spp), bacillus, 1665 subtilis accession number B-2 (Bacillus subtilis) AQ743(NRRL), bacillus, subtilis accession number B-21661 (Bacillus subtilis) AQ713(NRRL), bacillus, subtilis ATCC No. 55614 (Bacillus su btilis) AQ153(ATCC), bacillus, (Bacillus thuringiensis) BD #32 (NRRL Accession B-21530) thuringiensis, bacillus, thuringiensis B-21619 (Bacillus thuringie nsis) AQ52(NRRL Accession), muscodor, arbus (Mu scodor albus) 620(NRRL Accession No. HB 30547), muscodor, roseus (Muscodor roseus) A3-5(NRRL Accession No. HB 30548), rodokokkusu, accession number guroberurusu B-21663 (Rhodococcus globerulus) AQ71 9(NRRL), Marinomyces, 30232 accession number garubusu (Strepto myces galbus) (NRRL), accession number Marinomyces B-30145 (Streptomyces sp.) (NRRL spp), bacillus, thuringiensis, subgenuses, bacillus (Bacillus thuringiensis subspec.kurstaki) BMP123, taki Cruz, subtilis accession number B-50421 (Baci llus subtilis) AQ30002(NRRL) and bacillus, subtilis B-50455 (Bacillus subtilis) AQ30004(NRR L accession number), and/or, each of said microorganisms have all of the identifying characteristics of strain stock mutant, and/or, insects, mites, nematodes and/or to a plant pathogen activity produced by said microbial metabolites are individual selected from the group consisting 'of 1 and at least one type of insecticide' here, the insecticide, voltage-dependent sodium channel modulators and the sodium channel blocker is selected from the group consisting of ' 1 and optionally at least one type of a disinfectant, a plant, parts of plants, harvested fruits, vegetables and/or plant growth locus, in an amount effective to synergistically, simultaneously or successively applying to DMA_ADR (however, wherein the biological control agent and in the case where the sterilizing agent by, but not identical), wherein the method. 14. Wherein the sodium channel modulators/voltage-dependent sodium channel blockers and is or, pyrethroid, DDT, methoxychlor, indoxacarb and metaflumizone is selected from the group consisting of, method according to claim 13. 15. Kit, -, in part, at least two types of biological pesticide 1' here, the biological pesticide is, bacillus, accession number kichinosuporusu B-21618 (Bacillus chitinosporus) AQ746(NRRL), bacillus, YCpMmycl B-21664 (Bacil lus mycoides) AQ726(NRRL Accession), bacillus, pumilus B-30087 (Bacillus pumilus) (NRRL Accession), bacillus, pumilus B-21662 (Bacillus pumilus) AQ717(NRRL Accession), accession number 55608 bacillus (Bacillus sp.) AQ175(ATC C spp), accession number 55609 bacillus (Bacillus sp.) AQ177(AT CC spp), accession number 53522 Bacillus sp.AQ178(A TCC), bacillus, subtilis accession number B-21665 (Bacillus subtil is) AQ743(NRRL), bacillus, subtilis accession number B-21661 (Bac illus subtilis) AQ713(NRRL), bacillus, subtilis ATCC No. 55614 (Bacillus subtilis) AQ153(ATCC), bacillus, (Bacillus thuringie nsis) BD #32 (NRRL Accession B-21530) thuringiensis, bacillus, thuringiensis B-21619 (Bacillus thuringiensis) AQ52(NRRL Accession), muscodor, arbus (Muscodor albus) 620(NRR L Accession No. HB 30547), muscodor, roseus (Muscodor roseus) A 3-5(NRRL Accession No. HB 30548), rodokokkusu, accession number guroberurusu B-21663 (Rhodoco ccus globerulus) AQ719(NRRL), Marinomyces, 30232 accession number garubusu (Streptomyces galbus) (NRRL), accession number Marinomyces B-30145 (Streptomyces sp.) (NR RL spp), bacillus, thuringiensis, subgenuses, bacillus (Ba cillus thuringiensis subspec.kurstaki) BM P123, taki Cruz, b-50421 (Bacillus subtilis) AQ3000 2(NRRL subtilis accession number) and bacillus, subtilis accession number B-50455 (Bacillus subtilis) AQ30004(NRRL), and/or, as the above microorganism of all the identification of a strain of each of the stock has a characteristic of the mutant, and/or, insects, mites, nematodes and/or as the above microorganism is a plant pathogen which shows activity on metabolites produced by strains of the individual are selected from the group consisting 'of at least 1 kinds of insecticide and' wherein, the insecticide, sodium channel modulators and the voltage-gated sodium channel blocker is selected from the group consisting of ' the, synergistically effective amounts, in spatially separated locations comprising, said kit, -, parts. Claims amended 20170912 1. For controlling insectscomposition,barsils, subtilis (Bacillus subtilis) AQ713(NRRL Accession B-21661) andbacillus, subtilis (Bacillus subtilis) AQ30002(NRRL Accession B-50421) selected from the group consisting of at least 1 types of biological control agent andacrinathrin and lambda-sihirotoly1 an at least one type selected from the group consisting of insecticide comprises a, wherein said composition. 2. At least a disinfectant further comprising type 1 (however, the biological control agent and the disinfecting agent is, but not identical), claim 1tocomposition. 3. The disinfecting agent, selected from the group consisting of the following, wherein2composition: ergosterol biosynthesis inhibitors, complex I or II in the respiratory chain inhibitor, complex III in the respiratory chain inhibitor, mitosis and cell division inhibitors, host defenses that can elicit a compound, amino acid and/or protein biosynthesis inhibitors, ATP production inhibitors, cell wall synthesis inhibitors, lipid and membrane synthesis inhibitors, melanin biosynthesis inhibitors, of nucleic acid synthesis inhibitors, signal transduction inhibitor, a compound that can act as an uncoupling agent. 4. The disinfecting agent, selected from the group consisting of the following, the composition according to claim 2:binapacryl, dinocap, ferimzone, An, main heptyl gino cup, bench azole, betokisajin, kapushimaishin (capsimycin), carboxylic, kinomechioneto, piriofenon (kurazafenon (chlazafenone)), kufuranebu, cyflufenamid, cymoxanil, cyprosulfamide, dazomet, debakarubu, dichlorophen, jikuromejin, jifenzokoto, di fen zone court methyl sulfate, diphenylamine, ekomeito, fenpyrazamine, furumetoberu, furuoruimido, flusulfamide, furuchianiru, fosetyl-aluminum, fosetyl-calcium, fosetyl-sodium, hexachlorobenzene, irma clarithromycin, methasulfocarb, methyl isothiocyanate, metrafenone, mildiomycin, natamycin, nickel dimethyldithiocarbamate, nitorotaru-isopropyl, okuchirinon, okisamokarubu (oxamocarb), oxyphene ji inn (oxyfenthiin), pentachlorophenol and salts, phenothrin, phosphorous acid and its salts, propamocarb-hosechireto puropanoshin (propamocarb-fosetylate), -sodium (propanosine-sodium), purokinajido, pirimorufu, -3 - (2E) -3 - (4-tert - butylphenyl) (2-- chloropyridin -4 - - yl) prop - -1 - - ene (morpholin -4 - yl) on -1 - -2 -, -3 - (2Z) (4-tert - butylphenyl) (2-- chloropyridin -4 - yl) -3 - -1 - -1 - -2 - (morpholin -4 - yl) prop on encoding, pyrrolnitrin, tebufurokin, tecloftalam, torunifanido, triazoxide, torikuramido, ザリラミド, -8 - (3S, 6S, 7R, 8R) -3 - benzyl [( {3-[(isobutyryloxy) methoxy] -2 - - methoxypyridin - -4 - - yl} carbonyl) amino] methyl yl -7 - -6 - -1,5 - -4,9 - dioxo jiokisonan 2-methylpropanoate, 1-(4-{4-[(5R) -5 - (2,6 - difluorophenyl) oxazole -1,2 - -3 - - dihydro - -4,5 - yl] -1, 3-Thiazole -2 - yl} piperidin -1 - yl) -2 - [5-(trifluoromethyl) pyrazole -1H - -3 - -1 - methyl-l-yl] ethanone, 1-(4-{4-[(5S) -5 - (2,6 - difluorophenyl) -4,5 - dihydro -1,2 - oxazole -3 - yl] thiazole -2 - -1,3 - yl} piperidin -1 - yl) -2 - [5-(trifluoromethyl) pyrazole -1H - -3 - -1 - methyl-l-yl] ethanone, 1-(4-{4-[5-(2,6 - difluorophenyl) -4,5 - dihydro -1,2 - oxazole -3 - yl] thiazole -2 - -1,3 - yl} piperidin -1 - yl) -2 - [5-(trifluoromethyl) methyl pyrazole -1H - -1 - -3 - yl] ethanone, 1-dimethylbutane (4-methoxyphenoxy) imidazole carboxylate -1 - -3,3-1H - yl -2 -, -4 - tetrachloro - (methylsulfonyl) pyridine 2, 3, 5, 6 -, 2, 3-d chlorothieno -6 - dibutyl 2,3 -: -4 (3H) pyrimidine-ON, -1H dimethyl 2,6 -, 5H - [1, 4] dithiino [2, 3-c: 5, 6-c '] dipyrrole (2H, 6H) - 1, 3, 5, 7-Tetron, 2-[5-(trifluoromethyl) pyrazol - -3 - yl -1 - -1H - methyl] -1 - (4-{4-[(5R) -5 - phenyl -4,5 - - dihydro - -1,2 - oxazole -3 - yl] thiazole -2 - -1,3 - yl} piperidin -1 - yl) ethanone, 2-[5-(trifluoromethyl) pyrazol - -3 - yl -1 - -1H - methyl] -1 - (4-{4-[(5S) -5 - phenyl -4,5 - - dihydro - -1,2 - oxazole -3 - yl] thiazole -2 - -1,3 - yl} piperidin -1 - yl) ethanone, 2-[5-(trifluoromethyl) pyrazol - -3 - yl -1 - -1H - methyl] -1 - {4-[4-(5-phenyl -4,5 - - dihydro - -1,2 - oxazole -3 - yl) thiazole -2 - -1,3 - yl] piperidine -1 - yl} ethanone, 2-iodo-chromen - -4H - butoxy propyl -3 - -6 - on -4 -, 2-- chloro - -5 - [2-- chloro - -1 - (2,6 - - difluoro - -4 - methoxyphenyl) methyl imidazole -1H - -5 - -4 - yl] pyridine, 2-phenylphenol and salts, 3-( -1 - dimethyl -3,4 - dihydroisoquinoline trifluoro 4, 4, 5 - -3,3 - yl) quinolones, 3, 4, 5--2,6 - - Dicarbonitrile trichloropyridine^, 3-[5-(4-chlorophenyl) dimethyl -1,2 - -2,3 - - oxazolidin - -3 - yl] pyridine, 3-chloro -5 - (4-chlorophenyl) (2,6 - difluorophenyl) methylpyridazin -6 - -4 -, 4--3,6 - (4-chlorophenyl) (2,6 - difluorophenyl) dimethyl pyridazine -5 -, 5-thiadiazole - 1, 3, 4 - -2 - amino thiol, 5-chloro -N '- phenyl - N' - (-1 --prop - -2 - - yl) thiophene -2 - sulfonohydrazide, 5-fluoro [(4-fluorobenzyl) oxy] pyrimidine -4 - -2 - amine, 5-[(4-methylbenzyl) oxy] fluoro pyrimidine -4 - -2 - amine, 5-methyl octyl 1, 2, 4 -6 -: triazolo 1, 5-a: pyrimidine amine -7 -, -3 - (2Z) phenylpropanolamine -2 - amino -3 - cyano -2 - enoic acid ethyl, N'- (4-{[3-(4-- chlorobenzyl) thiadiazole - 1, 2, 4 - -5 - yl] oxy} -2,5 - dimethylphenyl) -N- ethyl -N- methyl imide formamide, N- -3 - (4-- chlorobenzyl) [3-methoxy -4 - (-2 --prop - -1 - yloxy) phenyl] propanamide, N- [methyl (4-- chlorophenyl) (cyano) ] -3 - [3-methoxy -4 - (-2 --prop - -1 - yloxy) phenyl] propanamide, N- [(5-- chloropyridin -3 - -2 - bromo-l-yl) methyl] carboxamide -3 - dichloropyridine -2,4 -, N- [1-(5-- chloropyridin -2 - - bromo - -3 - - yl) ethyl] carboxamide -3 - dichloropyridine -2,4 -, N- [1-(5-- chloropyridin -2 - - bromo - -3 - - yl) ethyl] carboxamide fluoro -2 - -3 - -4 - iodopyridine, N- {(E) -[(cyclopropylmethoxy) imino] methyl [6-(difluoromethoxy) -2,3 - difluorophenyl]} phenyIacetamide -2 -, N- {(Z) -[(cyclopropylmethoxy) imino] [6-(difluoromethoxy) -2,3 - difluorophenyl] methyl} phenyIacetamide -2 -, N' - {4-[(3-tert - butyl -4 - - cyano - -1,2 - thiazole -5 - yl) oxy] -2 - - chloro - -5 - methylphenyl} -N- methyl imide formamide ethyl -N -, n- Methyl -2 - (1-{[5-- methyl - -3 - (trifluoromethyl) -1H --pyrazol - -1 - yl] acetyl} piperidin -4 - yl) thiazole -1,3 - -N- -4 - (-1 - tetrahydronaphthalene 1, 2, 3, 4 - yl) carboxamide, methyl N- -2 - (1-{[5-- methyl - -3 - (trifluoromethyl) -1H --pyrazol - -1 - yl] acetyl} piperidin -4 - yl) -N- [-1 - - 1, 2, 3, 4 - tetrahydronaphthalene (1R) - yl] thiazole carboxamide -4 - -1,3 -, methyl N- -2 - (1-{[5-- methyl - -3 - (trifluoromethyl) -1H --pyrazol - -1 - yl] acetyl} piperidin -4 - yl) -N- [-1 - - 1, 2, 3, 4 - tetrahydronaphthalene (1S) yl] thiazole carboxamide -4 - -1,3 -, {6-[ ({[ (1-- methyl - -1H --tetrazol - -5 - yl) (phenyl) methylidene] amino} oxy) methyl] pyridine -2 - yl} carbamic acid pentyl, phenazine carboxylic acid -1 -, polyol -8 - quinoline, quinoline -8 - (2:1) all sulfates, {6-[ ({[ (1-- methyl - -1H --tetrazol - -5 - yl) (phenyl) methylene] amino} oxy) methyl] pyridine -2 - yl} carbamic acid tert - butyl, 1-methyl -3 - -N- (trifluoromethyl) [2 '- (trifluoromethyl) biphenyl - -2 - yl] pyrazole carboxamide -4 - -1H -, -3 - (4' - chlorobiphenyl -2 - yl) N- (difluoromethyl) pyrazole -1H - -1 - -4 - methyl carboxamide, N- (2 ', 4' - dichlorobiphenyl -2 - yl) methyl -1 - -1H - -3 - -4 - (difluoromethyl) pyrazole carboxamide, 3-- N- -1 - (difluoromethyl) methyl [4 '- (trifluoromethyl) biphenyl - -2 - yl] pyrazole carboxamide -4 - -1H -, N- (2', 5 '- difluorobiphenyl -2 - yl) methyl (trifluoromethyl) pyrazole carboxamide -4 - -3 - -1H - -1 -, 3-- N- -1 - (difluoromethyl) methyl [4' - (-1 --prop - -1 - - yl) biphenyl - -2 - yl] pyrazole carboxamide -4 - -1H -, 5--1 fluoro, 3-Dimethyl -N- [4 '- (-1 - - prop - -1 --yl) biphenyl - -2 - yl] pyrazole carboxamide -4 - -1H -, 2-- N- chloro [4' - (-1 - - prop - -1 --yl) biphenyl - -2 - yl] pyridine -3 - carboxamide, 3-- N- (difluoromethyl) [4 '- (3,3 - - dimethylbut-l-yl -1 - -1 -) biphenyl -2 - - yl] methyl -1 - -4 - -1H - pyrazole carboxamide, N- [4' - (3,3 - - dimethylbut-l-yl -1 - -1 -) biphenyl -2 - - yl] dimethyl pyrazole -1H - -1,3 - -4 - fluoro -5 - carboxamide, 3-(difluoromethyl) -N- -1H - -1 - (4 '- ethynylbiphenyl -2 - yl) methyl pyrazole carboxamide -4 -, -5 - (4' - ethynylbiphenyl -2 - yl) fluoro N- -1,3 - -1H - dimethyl pyrazole carboxamide -4 -, 2-(4 '- ethynylbiphenyl -2 - yl) -N- chloro pyridine -3 - carboxamide, 2-- N- chloro [4' - (3,3 - - dimethylbut-l-yl -1 - -1 -) biphenyl -2 - - yl] pyridine -3 - carboxamide, 4-- N- -2 - (difluoromethyl) methyl [4 '- (trifluoromethyl) biphenyl - -2 - yl] thiazole carboxamide -5 - -1,3 -, 5-- N- fluoro [4' - (3-- hydroxy - -3 --methylbut -1 - -1 - yl) biphenyl - -2 - yl] dimethyl pyrazole carboxamide -4 - -1H - -1,3 -, 2-- N- chloro [4 '- (3-- hydroxy - -3 --methylbut -1 - -1 - yl) biphenyl - -2 - yl] pyridine -3 - carboxamide, 3-- N- (difluoromethyl) [4' - (3-methoxy -3 - -1 - -1 - methylbut-l-yl) biphenyl - -2 - yl] methyl -1 --pyrazole - -1H - carboxamide -4 -, 5-- N- fluoro [4 '- (3-methoxy -3 - -1 - -1 - methylbut-l-yl) biphenyl - -2 - yl] dimethyl pyrazole carboxamide -4 - -1H - -1,3 -, 2-chloro -N- [4' - (3-methoxy -3 - -1 - -1 - methylbut-l-yl) biphenyl - -2 - yl] pyridine -3 - carboxamide, (5-- methylpyridin - -4 - - yl-methoxy -3 - bromo -2 -) (2, 3, 4 - trimethoxy -6 - methylphenyl) methanone, n - [2-(4-{[3-(4-chlorophenyl) prop - -2 ---1 - yl] oxy} -3 - - methoxyphenyl) ethyl] (methylsulfonyl) valinamide - N2-4-oxo -4 - [(2-phenylethyl) amino] butanoic acid, -1 - pig -3 --l-yl {6-[ ({[ (Z) -(1-- methyl - -1H --tetrazol - -5 - yl) (phenyl) methylene] amino} oxy) methyl] pyridine -2 - yl} carbamate, 4-amino -5 - fluoropyrimidine -2 - ol, propyl 3, 4, 5 - benzoic acids, and, orysastrobin. 5. The biological control agent(...)
最新评论
暂无评论。