MXPA97004725A - New insecticides and synergistic acaricides - Google Patents

New insecticides and synergistic acaricides

Info

Publication number
MXPA97004725A
MXPA97004725A MXPA/A/1997/004725A MX9704725A MXPA97004725A MX PA97004725 A MXPA97004725 A MX PA97004725A MX 9704725 A MX9704725 A MX 9704725A MX PA97004725 A MXPA97004725 A MX PA97004725A
Authority
MX
Mexico
Prior art keywords
spp
group
component
composition according
further characterized
Prior art date
Application number
MXPA/A/1997/004725A
Other languages
Spanish (es)
Other versions
MX9704725A (en
Inventor
Kern Manfred
Original Assignee
Hoechst Schering Agrevo Gmbh 13509 Berlin De
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from DE4445732A external-priority patent/DE4445732A1/en
Application filed by Hoechst Schering Agrevo Gmbh 13509 Berlin De filed Critical Hoechst Schering Agrevo Gmbh 13509 Berlin De
Publication of MX9704725A publication Critical patent/MX9704725A/en
Publication of MXPA97004725A publication Critical patent/MXPA97004725A/en

Links

Abstract

The present invention relates to insecticides and acaricides, characterized by an effective concentration of at least one insecticide compound selected from the group of the parapyrethroids, the group of the nitromethylenes, the group of the carbamates and the group of the phenylpyrazoles, in combination with the less a pathogenic fungus for insects (component

Description

NEW INSECTICIDES AND SYNERGISTIC RISKS Frequently, the potency of biological pesticides is insufficient to protect the c of useful plants, prly, against pests. For this reason, until now, preference has been given to chemical insecticides. It is intended an integrated cprotection to minimize the use of chemical substances, without having to accept simultaneously reduced yields. The publication of Soper and co-authors (1974, Enviromental Entomology, 3, 560-562) describes that the development of entomopathogenic fungi is inhibited by the simultaneous use of insecticides. When this depends on the type and amount of the agent used, it can be seen from the data that there is a powerful adverse effect on the development of the fungi. Filho and coauthors (1987, Biological, 53, 7-12, 69-70) also report that the development of Beauveria bassiana is inhibited by a variety of insecticides. EP 0 668 722 only describes that the fungus Beauveria bassiana can be used in combination with endosulfan. EP 0 627 165 describes environmental pathogenic fungi in combination with insecticides to control cockroaches.
Cft 2 086 351 further describes the use of entomopathogenic fungi together with insecticides to control termites. Surprisingly, biological experiments have now identified insecticides with a completely different structure that when used in conjunction with spores or particles of an entomopathogenic fungus show an excessively good activity against a broad spectrum of a variety of insects and mites. The present invention relates to insecticidal and acaricidal compositions comprising an effective amount of at least one insecticidal composition, selected from the group of parapyrethroids, the group of nitromethylenes, the group of carbamates and the group of phenylpyrazoles, in combination with at least one pathogenic fungus (component B). The invention particularly relates to compositions having the following insecticides, as components, in mixtures: (1) Parapyrethroids (pyrethroids other than ester) such as, for example, eilafluofen (4-ethoxyphenyl-C3- (4-fluoro- 3-phenoxyphenyl) pl] dimethylsilane, fil component of the formula I): and etofenpróx ((2- (4-ethoxyphenyl) -2-methylpl 3-phenoxybenzyl ether, component R2 of formula II): (2) Nitromethylenes, such as, for example, Imidacloprid (1- (6-chloro-3) -pyridylmet l) -N-nitroimidazolidin-2-ylidenearnine, component R3 of formula III): NI25 ((E) -NiC (6-chloro-3-pyridyl) methyl] -N2-cyano-Ni-methyl-acetamidine, component R4 of formula IV): Nitenpyram ((E) -N- (6-chloro-3-pyridylmethyl) -N-ethyl-N '-methyl-2-nitrovinylidene ina, component R5 of the formula (V)): (3) Carbamates, such as, for example: Phenoxycarb (ethyl 2- (4-phenoxyphenoxy) ethylcarbamate, component R6 of formula VI) (4) Phenylpyrazoles, such as, for example: Fipronil ((+) - 5-amino-1- (2,6-dichloro-a,, α-trifluoro-p-tolyl) -4-trifluoromethylsulfinyl-irazol-3- carbonitrile, component R7 of formula VII) The compounds mentioned above are all known in the literature ("Pesticide Nanual", 10th edition, Br.it. C Prot. Council, 1994) and are commercially available. A particularly interesting action against insects is shown by a mixture of silafluofen and fungi of the g + eneros Rcrernonioum, Rcanthomycee, Rschersonia, flspergillus, Beauveria, Culicinomyces, Engyodontium, Funicularis, F? Sarium, Gebellula, Hirsutella, Hymenstilbe, ri? Ta hiziurn, No uraea, Paecilo yces, Paraisaria, Pleurodesmopora, Polycephalo yces, Pseudogibellula,? orosporella, Sporothrix, "Stilbella", Tetracrium, Tetranacriurn, Tilachlidiurn, Tolypocladiu and Verticilliurn. All these genera are assigned to the section of Deuterornycota (Sarnson and coauthors, "Atlas of Entomopathogenic Fungi, 1988, Springer Verlag) .The fungi of the genera Hirsutella, Verticilliurn, fletarhiziuro, Beauveria, Paecilornyces and Nornuraea are of particular interest. The mycoinsecticide constituent may be present in a variety of forms: as conidiospores, as blastospores, as or sets of hy eae, as hyphal fragments or as a mixture of two or more of the forms mentioned above. In particular, the invention relates to insecticidal and acaricidal compositions comprising the fungus Beauveria bassiana or Metarhizium anisoplii. The fungus Beauveria bassiana has been described by Bassi, fl. (1836, C.R.Rcad, Sci. Paris 2, 434 to 436), Domsch, V.H. and co-authors (190, Compendium of Soil Fungi 1, 136-139) and Samson, R.R. and co-authors (1988, Atlas of Entomopathogenic Fungi, Springer-Verlag, Berlin) and obtainable from Mycotech (Butte, Montana, EUR), Hoechst Schering AgrEvo GmbH and Troy Sciences (formerly Fermone Corp.) (Phoenix, Rrizona, EUR ). In the text that follows, the term active substance is also used for each of the two components A or B. The mixing ratios of the two components can vary within wide limits. They depend in particular on the component used in the mixture, the stage of development of the pests and the climatic conditions. The invention also relates to compositions comprising the two components A and B in addition to the suitable formulation aids. The combinations of active substance according to the invention can exist not only as mixed formulations of the two components which are then diluted with water in the usual manner or applied as granules, but also in the form of so-called tank mixtures, by diluting together the components, which are formulated separately, with water. Based on these formulations, it is also possible to prepare combinations with other pesticidally active substances, such as selective herbicides and fungicides or specific insecticides, and also fertilizers and / or growth regulators, for example, in the form of a ready-to-use mixture. or of a tank mix. The components can be formulated in a variety of ways, depending on the biological and / or chemophysical parameters that prevail. The appropriate formulation options are, for example; yeast formulations, starch formulations, wettable powders (PH), emuleifi cable concentrates (CE), aqueous solutions (SL), emulsions (EU), such as oil-in-water and water-in-oil emulsions, spray solutions or emulsions, water-based or oil-based dispersions, it assumes ions, powders (DP), seed treatment products, granules for application or spreading in the soil, or water-dispersible granules (UG), ULV formulations, microcapsules or baits (substrates) . Particularly interesting are oil-in-water and water-in-oil emulsions, wettable powders or granules. These individual types of formulation are known in principle and are described, for example, in: Uinnacker-Küchler, "Chemische Technologie" ["Chemical Technology3, volume 7, C. Hauser Verlag Munich, 4th edition, 1986; van Valkenburg," Pesticide Formulations ", Marcel Dekker, NY, 2nd edition, 1972-73, K. Martens," Spray Drying Handbook ", 3rd edition, G. Goodwin Ltd. London, The required formulation aids, such as inert materials , surfactants, solvents and other additives are also known and described, for example, in: Uatkins "Handbook of Insecticide Dust Diluents and Carriers," 2nd edition, Darland Books, Caldwell, NJ; H. v. Olphen, " Introduction to Clay Colloid Chernistry, 2nd edition, 3. Uiley R Sons, NY, Marsden "Solvents Guide", 2nd edition, Interscience, NY, 1950, McCutcheon's, "Detergents and Ernulsifiers Annual", MC Publ. Corpl, Ridge ood, N.3; Sieley and Uood, "Encyclopedia of Surface Active Agents", Chem .. Pu Bl. Co. Inc., N.Y., 1964; Schonfeldt, "Grenxfláchenaktive fithylenoxidaddikte" Surfactant additives of ethylene oxide], Uíss. Verlagsgesell, Stuttgart 1976; Uinnacker-Küchler, "Chemische Technologie" [Chemical Technology} , volume 7, C. Hauser Verlag Munich, 4th. Edition, 1986. Wettable powders are preparations which are uniformly dispersed in water and which, in addition to the active substance, also comprise wetting agents, for example, polyoxyethylated alkyl phenols, polyoxyethylated fatty alcohols or fatty amines, alkanesulfonates or alkylbenzenesulfonates and dispersants. , for example, sodium lignosulfonate, Sodium 2,2'-dinaphthylmethane-6,6'-disulfonate, sodium dibutylnaphthalene sulfonate or even sodium oleoylmethyltaurinate, in addition to the diluent or the inert substance. The emulsifiable concentrates are prepared by dissolving the active substance in an organic solvento, for example, butane, cyclohexanone, dirnethylformamide, xylene or high-boiling compounds or aromatic hydrocarbons, with the addition of one or more emulsifiers. Examples of the emulsifiers that may be used are: calcium alkylarylsulfonate, such as calcium dodecylbenzenesulfonate or nonionic emulsifiers, such as polyglycol fatty acid esters, polyglycolyl alkylaryl ethers, fatty alcohol polyglycol ethers, oxide condensates of propylene / ethylene oxide, alkyl polyethers, sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid esters or polyoxyethylene sorbitol esters. Powders can be obtained by grinding the active substance with finely divided solid substances, for example, talc, natural clays, such as kaolin, bentonite and pyrophyllite and diatomaceous earth. Granules can be produced either by spreading the active substance on an inert adsorbent, granulated material, or by applying concentrates of active substance on the surface of carriers, such as sand, kaolinites or granulated inert material, by means of binders, for example, alcohol. polyvinyl, sodium polyacrylate or, alternatively, mineral oils. It is also possible to granulate suitable active substances in the manner that is conventional for the production of fertilizer granules, if desired, in a mixture with fertilizers. As a general rule, the agrochemical preparations comprise from 0.0001 to 99 weight percent, in particular-between 0.0005 and 95%, preferably between 2 and 90% of the two components A and B. The low concentrations, that is, 0.0001 at 2%, they are advantageously used to control undesirable social insects, as has been suggested in P 44 03 062.2. The concentrations of active substances A and B may differ in the formulations. The concentration of active substance in wettable powders, for example, is about 10 to 90 weight percent; the remainder up to 100 weight percent is composed of conventional formulation components. In the case of concentrates and ulsifiable, the concentration of active substance can be from 1 to 90 weight percent, preferably from 5 to 80 weight percent. Formulations in the form of powders comprise about 1 to 30 weight percent, preferably 5 to 20 weight percent, of active substance; the sprayable solutions are from about 0.05 to 80 weight percent, preferably from 2 to 50 weight percent of active substance. In the case of granules, for example water-dispersible granules, the content of active substance depends partly on whether the active compound is in the liquid or solid form and on the granulation auxiliaries and fillers that are used. As a rule, water-dispersible granules comprise between 1 and 95 weight percent; the granules to spread between 1 and 50%, preferably between 2 and 25%. The baits have an active substance content of between 0.0001 and 10%, with respect to component 1. The use concentration can vary between 0.1 ppm (equivalent to 0.0001 g / liter) and 10,000 ppm (equivalent to 10 g / liter), preferably between 0.5 and 5,000 ppm, particularly between 5 and 1,000 ppm. A mixture that has been shown to be effective comprises the insecticidal component and a mycoinsecticide component, used in a proportion such that the content of component A reaches up to 0.01 and 50%, preferably from 0.1 to 50%; and the amount of the ico-insecticide up to 102 to 10 * 5 spores, preferably 105 to 1012 spores, or between 0.01 g and 1,000 g of the formulated substance. In addition, the active substance formulations comprise, if appropriate, the adhesives, wetting agents, dispersants, emulsifiers, penetrants, solvents, fillers or carriers that are conventional in each case. For use, the formulations which are present in commercially obtainable form, are diluted if appropriate, in a customary manner, for example, using water in the case of wettable powders, emulsifiable concentrates, dispersions and dispersible granules in Water. Preparations in the form of powders or granules for application to the soil or the solutions of spreading and spraying frequently are not further diluted with other inert substances, before use. Component B can be formulated, for example, as described by Prior, C. and co-authors in the Journal of Invertebrale Pathology 52, 66-72 (1988). Preferably, component B is formulated as proposed in P 44 04 702.9. The rate of application of the required mixture varies with external conditions, such as, for example, temperature, humidity and the like. It also depends on the particular field of application and the plant to be treated; and therefore may vary within wide limits. It is between 1 g / ha and 200 g / ha, preferably between 20 g / ha and 100 g / ha, particularly preferably between 40 g / ha and 80 g / ha, in the case of component A (for example, silafluofen) . In the case of the entomopathogenic fungus, it is between 10 g of conidia / ha and 1,000 g of conidia / ha, preferably between 20 g of conidia / ha and 400 g of conidia / ha. 108 to 100 g of conidia of an opathogenic fungus are approximately 1 g. The two components A and B can be applied simultaneously or in succession. It makes sense to carry out the second application after the first one has dried on the plant, in order to avoid undesirable flushing of the first component. The combination of component (A) and entomopathogenic fungi is well tolerated by plants, has a favorable toxicity for warm-blooded species and is suitable for controlling pests of animals in agriculture, particularly insects and arachnids. The synergistic mixture of the two components is active against the normally sensitive and resistant species and against certain stages of development. The compositions according to the invention have an outstanding insecticidal activity against a broad spectrum of economically important pests. Some representatives of the pests that can be controlled with the compositions according to the invention can be mentioned individually, by way of example, but this is not intended to be a limitation to certain species. From the order of the isopods, for example, they can cite Oniscus asellus, Armadium vulgare and Porcellio scaber., From the order of the diplopopods, for example, Blaniulus guttalatus. From the order of the chilopoda, for example, Geophilus carpophagus and Scutigera spec. From the order of the sinfilos, for example, Scutigerella i maculata. From the order of the tisan? Ros, for example, Lepisma saccharina. From the order of springtails, for example, Onychiurus arrnatus. From the order of the orthoptera, for example, Blatta orientalis, Periplaneta americana, Leucophaea maderae, Blattella germ nica, Acheta do esticus, Grillotalpa spp., Locusta migratoria rnigratorioides, Melanoplus di ferentialis and Schistocerca gregaria. From the order of dermápteros, for example, Forfícula auricularia. From the order of the anopluros, for example, Phylloxera vastatrix, Pe phigus spp., Pediculus hu anus corporis, Haematopinus spp. and Linognathus spp. From the order of the malophagus, for example, Tricodectes spp. And Darnalinea spp. From the order of the tisanópeteros, for example, Hercinothrips femoralis and Trips tabaci. From the order of the heteroptera, for example, Eurygaster spp., Dysdercus intermedi? S, Pies a quadrata, Cimex lectularius, Rhodnius prolixus and Triatoma spp. From the order of Homoptera, for example, Rleurodes brassicae, Bemisia tabaci, Trialeurodes vaporariorum, Aphis gossypii, Brevicoryne braseicae, Cryptomyzus ribis, Doralis fabae, Doralie po I, Eriosorna lanigerum, Hyalopterus arundinis, Macrosiphum avenae, Myzus spp., Phorodon hu uli , Rhopalosiphurn p >; adi, E poasca spp., Euscelis bilobatus, Nep otettis cincticeps, Lecanium corni, Saiseetis oleae, Laodelphax striatellus, Nilaparvata lugens, Aonidiella aurantii, Aspidiotus hederae, Pseudococcus spp. and Peylla spp. From the order of the Lepidoptera, for example, Pectinophora gossypiella, Bupalus piniarius, Cheimatobia brumata, Lithocolletie blancardella, Huyponomeuta padella, Plutella maculipennis, Harassment to neustria, Euproctis chrysorrhoea, Lumantria spp., Buvulatrix thurberiella, Phyllocnietis citrella, Agrotis spp., Euxoa spp., Feltia spp., Earias insulana, Heliothis spp., Laphygma exigua, Ma estra brassicae, Panolis flammea, Prodenia litura, Spodoptera spp., Trichoplusia ni, Carpocapsa pomonella, Perileucoptera coffeella, Pieris spp., Chilo spp., Pyrausta nubilalis , Epheetia kuehniella, Galleria rnelloneila, Tineola bisselliella, Tinea pellionella, Hofmannophila pseudospretella, Cacoecia podana, Capua reticulana, Choristeneura furniferana, Clysia ambiguella, Homona magnanimous, Tortrix viridana. From the order of coleoptera, for example, Anobium punctatum, Hypotheus enus ha pei, Rhizopertha dominica, Bruchidius obtectus, Acanthoscelides obtectus, Hylotrupes bajulus, Agelastica alni, Leptinotarsa decemlineata, Phaedon cochleariae, Diabrotica spp., Psylliodes chrysocephala, Epilachna varivestis, Atomaria spp. , Oryzaephilus surina ensis, Anthonomus spp., Sitophilus spp., Otiorrhynchus sulcatus, Cosmopolites sordidus, Ceuthorrhynchus assimilis, Hypera postica, Der estes spp., Trogoder spp., Anthrenus spp., Attagenus spp., Lyctus spp., Meligethes aeneus, Ptinus spp., Niptus lololeucus, Gibbiurn psylloides, Tribolium spp., Tenebrio molitor, Agriotes, spp., Conoderus spp., Melolontha melolontha, Amphi allon solstitialis and Costelytra zealandica. From the order of the hyoptera, for example, Diprion spp., Hoplocampa spp., Lasius spp., Mono oriu pharaonis and Vespa spp. From the order of the iopterous, the families Mastotermitidae, Kalotermitidae, Hodotermitidae (in particular Hodotermitinae, Termopeinae), Rhonoter itidae (in particular Coptoter itinae, Heterotermitinae, Psammotermitínae), Termitidae (in particular, Macroter itinae, Nasutiterrnitinae, Termitinae), for example, Mastoter is sp., Such as Maetroter is Darwiniensis, Cryptotermes sp., Incistitermes sp., Kalotermes sp., Such as Kalotermes flavicollis, Marginiter is ep. , Anacothotermes sp., Zootermopsis sp., Coptoter sp., Such as Coptotermes formosanus, Heterotermes sp. , Psarnrnotermes sp., Prorhinoter sp., Schedorhinotermes sp., Allodontermes sp., Nasutitermes sp., Termes sp., Ami ermes sp., Globitermes sp. , Microceroterrnes sp., Oniscus asellus, Armadium vulgare, Porcellio scaber, Reticulitermes sp. , such as Reticulitermes flavipers, Reticulitermes lucifugus. The use of the active substance combinations according to the invention, in particular silafluofen and fipromil in combination with Beauveria bassiana, results in a particularly advantageous activity against termites of the family Kalotermitidae, such as, for example, Cryptotermes cubioceps, Kalotermes spp., Or of the family Rhinoterrniti ae, such as, for example, Coptotermes for osus, Heteroter ee spp, or of the family Terrnitidae, such as, for example, Nasutitermes spp., Or of the family Mastotermitidae, such as, for example, Mastoter is to give iniensis. From the family of Formicidae, for example, Atta cephalotes, Lasius niger, Lasius brunneus, Componotus ligniperda, Monomoriurn pharaonis, Solenopsis gerninata, Monomorium minimum, Irido yres hu ilis, Dorylus sp., Exition sp. Of the superfa ilia of the Vespoideas, for example, German Vespa, Vespa vulgaris, Vespa media, Vespa saxonica, Vespa crabro, Vespula acalata, Polistes nyrnpha, Vespa orintalis, Vespa mandarinia, Vespa velutina. Of the superfamily of the Apoideas, one can mention the murderous bees. From the order of the dipterans, for example, Aedes spp., Anophelee spp., Culex spp., Drosophila melanogaster, Musca spp., Fannia spp., Calliphora erythrocephala, Lucilia spp., Chrysomyia spp., Cuterebra spp., Gastrophilus spp. , Hyprobosca spp., Stomoxys spp., Oestrus spp., Hypoder spp., Tabanus spp., Tannia spp., Bibio hortulanus, Oscinella frit, Phorbia spp., Pegomyia hyoscyami, Ceratitis capitata, Dacus oleae and Typula paludosa. From the order of the siphonoptera, for example, Xenopsylla cheopis and Ceratoplyllus spp. From the order of arachnids, for example, Scorpio maurus and Latrodectus mactans. From the order of the acarines, for example, Acarus siro, Argas spp., Ornithodoros spp., Dermanyseus gallinae, Eriophyee ribis, Phyllocoptruta oleivora, Boophilus spp., Rhipicephalus spp., Amblyo rna spp., Hyalo ma spp., Ixodes spp. , Psoroptes spp., Chorioptes spp., Sarcoptes spp., Tarsonemus spp., Bryobia praetiosa, Panonychus spp. and Tetranychus spp. The combination according to the invention of silafluofen and entomopathogenic fungi is particularly suitable for controlling sensitive and resistant insects Heliothis spp., Anthono us epp. , Hupotheus emus harnpei, Spodoptera spp., Nephotettis spp., Nilaparvata lugens, Trichoplusia spp., Leptinotarsa decemlineata and other feeder insects (termites, ants) and suckers, such as whiteflies or spider mites. The combinations of active substance according to the invention allow insecticidal and acaricidal activity to be obtained in excess of that which is expected based on the activity of the individual components. This increase in activity allows the application regimes of the individual active substances to be considerably reduced. The combination of the active substances can also improve their long-term activity or cause the acceleration of the speed of activity. Said properties are considerably advantageous for the user who will control the insects in practice. They allow insects to be controlled more economically and more quickly, with less work and for longer periods, which means that better yields can be obtained in the population of crop plants. Another increase in activity can be achieved by using so-called feeding or phago-staging attractions, such as, for example, Konsurne (from Pharrnone), ATPlus, yeast, starch, Stirr? P (from Arochern, North America, Inc., USA) and Coax. Although the compositions according to the invention have an outstanding insecticidal and acaricidal activity, the crop plant is not damaged at all. For this reason, the compositions are particularly suitable for cotton, soybeans and rice crops. It is very particularly advantageous to use it in rice and tea culture, because the climatic conditions are particularly advantageous for both products. They are also suitable for controlling pests in coffee, fruit and vegetable production, or in viticulture. The following examples are intended to illustrate the invention without imposing any restrictions: A.- BIOLOGICAL EXAMPLES In all cases, a differentiation was made between the calculated degree and the degree of effectiveness found in the combinations. If the actual damage exceeds the expected damage by calculation, then the activity of the combination is superadditive, that is, there is a synergistic effect. The combinations of active substance according to the invention have an insecticidal activity exceeding that which is expected based on the expected activities of the individual components, when used by themselves. This means that the combinations of active substance are synergistic.
EXAMPLE 1 SPODOPTERA LITTORALIS IN COMBINATION WITH SILAFLUOFEN It was sprayed with the active substances or mixtures of them, larvae resistant to the pyrethroids of the Egyptian cotton leafworm (Spodoptera littoralis, L 3), together with a suitable food. The effect of the individual components and the ezclae of the individual components was determined six days after maintaining the test material at 25 ° C and at an atmospheric humidity of 80%.
EXAMPLE 2 ANTHONOMUS GRANDIS IN COMBINATION WITH SILAFLUOFEN Adult samples of the cotton weevil (Anthonomus grandis) were sprayed together with suitable food (synthetic feed), with the active substances or their mixtures. The effect of the individual components and mixtures of individual components was determined 9 days after maintaining the test material at 25 ° C and at a relative atmospheric humidity of 90%. 00 EXAMPLE 3 NILAPARAVATA LUGENS IN COMBINATION WITH SILAFLUOFEN Larvae of the rice grasshopper (Nilaparvata lugens) were placed on rice plants that had previously been immersed in aqueous solutions composed of active substances or their mixtures. The effect of the individual components or mixtures of individual components was determined six days after maintaining the test material at 25 ° C and at a relative atmospheric humidity of 80%.
EXAMPLE 4 NILAPARVATA LUGENS IN COMBINATION WITH ETOFENPROX Rice grasshopper (Nilaparvata lugens) larvae that had been previously immersed in aqueous solutions of active substances or their mixtures were placed on rice plants. The effect of the individual components or mixtures of the individual components was determined six days after maintaining the test material at 25 ° C and at a relative atmospheric humidity of 80%.
Substance Active substance in% active Mortality / ppm component Etofenprox (Al) 63 100 31 70 16 30 8 0 4 0 2 0 Beauveria 2.3 lQio conidia / ha 28 bassiana (B) (Naturalis-L) (A) + (B) Per In the exálculo perimento (A2) + (B) 63 + 2.3 1010 100 100 31 + 2.3. irjio 98 100 16 + 2.3 1010 58 80 8 + 2.3 • 1010 28 80 4 + 2.3. 1010 28 60 2 + 2.3 • 1010 28 40 EXAMPLE 5 NILAPARVATA LUGENS IN COMBINATION WITH IMIDACLOPRID Rice grasshopper (Nilaparvata lugens) larvae that had been previously immersed in aqueous solutions of active substances or their mixtures were placed on rice plants. The effect of the individual components or mixtures of individual components was determined six days after maintaining the test material at 25 ° C and at a relative atmospheric humidity of 80%.
EXAMPLE 6 SPODOPTERA LITTORALIS IN COMBINATION WITH NI25 The larvae were sprayed with the active substances or with their mixtures resistant to the pyrethroids of the Egyptian cotton leafworm (Spodoptera littoralis, L 3), together with the adequate diet. The effect of the individual components or mixtures of individual components was determined six days after maintaining the test material at 25 ° C and at a relative atmospheric humidity of 80%.
EXAMPLE 7 NILAPARVATA LUGENS IN COMBINATION WITH NITENPYRAM (TI-304) Larvae of the ricehopper (Nilap > arvata lugens) were placed on rice plants that had previously been immersed in aqueous solutions of the active substances or their mixtures. The effect of individual components or mixtures of individual components was determined six days after maintaining the test material at 25 ° C and at a relative atmospheric humidity of 80%. fifteen twenty O R EXAMPLE 8 SPODOPTERA LITTORALIS IN COMBINATION WITH FENOXYCARB The larvae were sprayed with the active substances or with their mixtures, resistant to the pyrethroid of the Egyptian cotton leafworm (Spodoptera littoralis, L 3), together with adequate feeding. The effect of the individual components or mixtures of individual components was determined 6 days (10 days in the case of Fenoxycarb) after maintaining the test material at 25 ° C and at a relative atmospheric humidity of 80%.
EXAMPLE 9 SPODORA LITTORALIS IN COMBINATION WITH FIPRONIL The larvae were sprayed with the active substances or with their mixtures resistant to the pyrethroids of the Egyptian cotton leafworm (Spodoptera littoralis, L 3), together with the adequate diet. The effect of the individual components or mixtures of individual components was determined 6 days after maintaining the test material at 25 ° C and at a relative atmospheric humidity of 80%.
EXAMPLE 10 ANTHONOMUS GRANDIS IN COMBINATION WITH FIPRONIL The samples of adults of the cotton weevil (Anthonomus grandis) were sprayed with the active substances or with their mixtures together with suitable food (synthetic food). The effect of the individual components or mixtures of individual components was determined 9 days after maintaining the test material at 25 ° C and at a relative atmospheric humidity of 90%.

Claims (7)

NOVELTY OF THE INVENTION CLAIMS
1. An insecticidal and / or acaricidal composition, characterized in that it comprises an effective content of at least one insecticide compound selected from the group of nitromethylenes, the group of pyrethroids which are not esters, the group of carbamates and the group of phenylpipes razóles (component A); and at least an entomopathogenic fungus (component B) where, in the case that the fl component is nitromethylene, component B is Beauveria bassiana and the latter combination is not used to control isoptera.
2. A composition according to claim 1, further characterized in that the mycoinsecticide is selected from the group of the genera Hirsutella, Verticillium, Metarhiziurn, Beauveria, Paecilornyees or Nomouraea.
3. A composition according to claim 1, further characterized in that the mycoinsecticide used is Bea? Veria bassiana.
4. A composition according to claim 1, further characterized in that it comprises an effective content of at least one compound selected from the group consisting of Silafluofen, Etofenprox, Imidacloprid, (E) -Ni - [(6-chloro- 3-pi id1) rnet.il] -N-cyano-Ni-methylacetamidine, Nitempyrarn, Fenoxycarb and Fipronil.
5. A composition according to claim 1, further characterized in that the mycoinsecticide is composed of blasto- spores.
6. A composition according to claim 1, further characterized in that the mycoinsecticide is composed of mycelia or mycelial fragments.
7. An insecticidal and / or acaricidal composition, characterized in that it comprises from 1 to 99 weight percent of a composition as claimed in claim 1, in addition to the usual formulation auxiliaries.
MXPA/A/1997/004725A 1994-12-21 1997-06-23 New insecticides and synergistic acaricides MXPA97004725A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE4445732A DE4445732A1 (en) 1994-12-21 1994-12-21 New synergistic means to control insects and acarina
DEP4445732.4 1994-12-21
PCT/EP1995/004897 WO1996019112A1 (en) 1994-12-21 1995-12-12 New synergistic insecticides and acaricides

Publications (2)

Publication Number Publication Date
MX9704725A MX9704725A (en) 1997-10-31
MXPA97004725A true MXPA97004725A (en) 1998-07-03

Family

ID=

Similar Documents

Publication Publication Date Title
US5888989A (en) Synergistic compositions for controlling insects and acarina
US5631276A (en) Synergistic compositions for controlling insects and acarina
US5730973A (en) Water-dispersible granules of spores or live Beauveria bassiana
US5703132A (en) Synergistic combinations of ammonium salts
US5804208A (en) Granulates containing micro-organisms
KR100420161B1 (en) Insecticides
US4857510A (en) Compositions for combating pests containing macrocyclic lactones
KR20000028735A (en) Active compound combinations having insecticidal and acaricidal properties
KR20090028800A (en) Active ingredient combinations with insecticidal and acaricidal properties
US20130190260A1 (en) Active agent combinations
JP4846098B2 (en) Use of spinosyns as soil killing insecticides
JP2002532394A (en) Activator combinations
JP2802315B2 (en) Pest control agent
MXPA97004725A (en) New insecticides and synergistic acaricides
JP2002532396A (en) Combination of active ingredients
US5139785A (en) Pesticides