DK144141B - FROEMATERIAL TREATED WITH INSECTICID - Google Patents
FROEMATERIAL TREATED WITH INSECTICID Download PDFInfo
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- DK144141B DK144141B DK81176AA DK81176A DK144141B DK 144141 B DK144141 B DK 144141B DK 81176A A DK81176A A DK 81176AA DK 81176 A DK81176 A DK 81176A DK 144141 B DK144141 B DK 144141B
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
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- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
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Description
(19) DANMARK (w) f\Ra/(19) DENMARK (w) f \ Ra /
02) FREMUEGGELSESSKRIFT nn 1441 41 B02) PROCEDURE WRITING nn 1441 41 B
DIREKTORATET FOR PATENT- OG VAREMÆRKEVÆSENETDIRECTORATE OF THE PATENT AND TRADEMARKET SYSTEM
(21) Ansøgning nr. 8ll/76 (51) Int.CI.3 A 01 N 47/22 (22) Indleveringsdag 26. feb. 1976 (24) Løbedag 26. feb. 1976 (41) Aim. tilgængelig 28. aug. 1976 (44) Fremlagt 21. dec. 1981 (86) International ansøgning nr. - (86) International indleveringsdag - (85) Videreførelsesdag - (62) Stamansøgning nr. - (30) Prioritet 27. feb. 1975* 8267/75* GB (71) Ansøger FISONS LIMITED, London, GB.(21) Application No. 8ll / 76 (51) Int.CI.3 A 01 N 47/22 (22) Filing Date Feb 26 1976 (24) Running day Feb 26 1976 (41) Aim. available Aug. 28 1976 (44) Presented 21 Dec. 1981 (86) International Application No. - (86) International Filing Day - (85) Continuation Day - (62) Master Application No. - (30) Priority Feb 27 1975 * 8267/75 * GB (71) Applicant FISONS LIMITED, London, GB.
(72) Opfinder peter John Brooker, GB: Quinton Ashton Geering, GB.(72) Inventor Peter John Brooker, GB: Quinton Ashton Geering, GB.
(74) Fuldmægtig Internationalt Patent-Bur eau.(74) Clerk of the International Patent Office.
(54) Frømateriale behandlet med in=* sekticid.(54) Seed material treated with in = * secticide.
Opfindelsen angår frømateriale behandlet med insekticid, hvilket frømateriale er ejendommeligt ved, at det indeholder fra 0,1 g til 28 g, fortrinsvis højst 18 g, og mere foretrukket fra 0,25 g til 10 g, 2,2-dimethyl-l,3-benzodioxol-4-yl-N-methylcar-bamat pr. kg frø.The invention relates to insecticide-treated seed material which is characterized in that it contains from 0.1 g to 28 g, preferably not more than 18 g, and more preferably from 0.25 g to 10 g, 2,2-dimethyl-1. 3-benzodioxol-4-yl-N-methylcarbamate per kg of seeds.
Med udtrykket "behandlet" menes her, at frøene enten er i inderlig blanding med 2,2-dimethyl-l,3-benzodioxol-4-yl-N-m methylcarbamatet eller er overtrukket hermed. Fortrinsvis er frøene ^ behandlet med carbamatet enten ved pudring med et tørt middel eller t— ved en sædvanlig sprøjte-overtrækningsteknik, ved hvilken carbama- tet er opløst eller dispergeret i et flygtigt opløsningsmiddel, som T— * □ 2 U4U1 sprøjtes på frøene og bortdampes herfra, eller ved en konventionel pelleteringsproces, ved hvilken carbamatet er blandet med en fast bærer, f.eks. ler eller træmel, og frøene overtrækkes med denne blanding. Selvsagt vil den teknik, der vælges, i nogen grad afhænge af hvilke frø, der skal behandles. Frø, som kan behandles, omfatter f.eks. grøntsager, specielt kålarter, løg og bønner (f.eks. soyabønner), kornarter, specielt hvede, byg, havre og majs, og rodafgrøder, specielt sukkerroer. Behandlingen, der udøves til hver type frø, vil sædvanligvis afhænge af den konventionelle behandling til den pågældende frøtype. Således vil sukkerroefrø, som ofte pelleteres, sædvanligvis behandles ved en pelletering. Kornsorter, der imidlertid sædvanligvis ikke pelleteres, vil fortrinsvis behandles, ved pudring eller sprøjtning.By the term "treated" is meant herein that the seeds are either in intimate admixture with the 2,2-dimethyl-1,3-benzodioxol-4-yl-N-m methylcarbamate or are coated therewith. Preferably, the seeds are treated with the carbamate either by drying with a dry agent or by a conventional spray coating technique in which the carbamate is dissolved or dispersed in a volatile solvent which is sprayed onto the seeds and evaporated. from this, or by a conventional pelletizing process in which the carbamate is mixed with a solid support, e.g. clay or wood flour, and the seeds are coated with this mixture. Of course, the technique chosen will depend to some extent on the seeds to be processed. Treatable seeds include e.g. vegetables, in particular cabbage, onions and beans (eg soybeans), cereals, especially wheat, barley, oats and corn, and root crops, especially beet. The treatment applied to each type of seed will usually depend on the conventional treatment for that type of seed. Thus, sugar beet seeds, which are often pelleted, will usually be processed by a pelleting. However, cereals which are not usually pelleted will preferably be treated, by powdering or spraying.
De behandlede frø ifølge opfindelsen udviser en overraskende høj spiringsevne og evne til at videreudvikle spirerne , under tilstedeværelse af insektskadedyr, og det har endvidere vist sig, at carbamatet overraskende kan absorberes systemisk af småplanterne til opnåelse af modstandsdygtighed mod insektangreb,efter at planterne er kommet frem af jorden.The treated seeds according to the invention exhibit a surprisingly high germination ability and ability to further develop the germs in the presence of insect pests, and it has further been found that the carbamate can be surprisingly absorbed systemically by the small plants to achieve resistance to insect infestation after the plants have emerged. of the earth.
2,2-Dimethyl-l,3-benzodioxol-4-yl-N-methylcarbamat er en kendt forbindelse, der har fundet anvendelse som insekticid under navnet Bendiocarb til bekæmpelse af f.eks. kakerlakker.2,2-Dimethyl-1,3-benzodioxol-4-yl-N-methylcarbamate is a known compound which has been used as an insecticide under the name Bendiocarb to control e.g. cockroaches.
Derimod har forbindelsen ikke tidligere været foreslået til behandling af frø, og det har for fagmanden været overraskende, at den har vist sig egnet hertil.In contrast, the compound has not previously been proposed for the treatment of seeds, and it has been surprising to those skilled in the art that it has proved suitable for this purpose.
For at et insekticid er egnet til behandling af frømateriale, må det opfylde visse væsentlige krav, som er særdeles vanskelige at tilfredsstille. Da frøene anbringes i jorden, er det selvsagt nødvendigt, at insekticidet er stabilt i jordbunden og forbliver her tilstrækkeligt længe til at hindre skader forårsaget af insektangreb under de allertidligste trin af plantens udvikling. Forbindelsen må selvsagt også være praktisk taget ikke-phytotoxisk.In order for an insecticide to be suitable for the treatment of seed material, it must meet certain essential requirements which are extremely difficult to satisfy. Since the seeds are placed in the soil, it is of course necessary that the insecticide is stable in the soil and remains here long enough to prevent damage caused by insect infestation during the earliest stages of plant development. Of course, the compound must also be practically non-phytotoxic.
Jordbunden udgør et særdeles ugunstigt miljø for pesticider. Blandt de faktorer, der medvirker til at nedbryde ethvert pesticid, er den stadige tilstedeværelse af vandig fase, sollysets indvirkninger, indvirkninger af jordbundens mikroorganismer og temperatursvingninger. Betingelserne er så vanskelige, at de eneste 144141 3 alment tilgængelige insekticider til anvendelse i jordbunden har været sådanne, som faldt inden for den gruppe, der er kendt som de organiske chlorholdige insekticider, som udmærker sig ved deres ekstreme stabilitet og modstandsdygtighed. Alle andre typer insekticider har hidtil vist sig at være utilstrækkeligt stabile og/eller at være phytotoxiske.Soil constitutes a particularly unfavorable environment for pesticides. Among the factors that help to break down any pesticide are the constant presence of aqueous phase, the effects of sunlight, the effects of soil microorganisms and temperature fluctuations. The conditions are so difficult that the only widely available insecticides for use in the soil have been those which fall within the group known as the organic chlorine-containing insecticides which are distinguished by their extreme stability and resilience. All other types of insecticides have so far been found to be insufficiently stable and / or to be phytotoxic.
Carbamater er som følge af deres kemiske struktur i høj grad udsatte for hydrolyse, og der findes talrige arbejder, der angiver dette som årsag til, at sådanne materialer sædvanligvis ikke kan anvendes i jordbunden.Because of their chemical structure, carbamates are highly susceptible to hydrolysis, and numerous works exist which indicate this as the reason that such materials are usually not usable in the soil.
2,4-Dimethyl-l,3-benzodioxol-4-yl-N-methylcarbamat har imidlertid som nævnt overraskende vist sig at kunne anvendes til behandling af frø til opnåelse af en passende beskyttelse i jordbunden i et tilstrækkeligt langt tidsrum. Dette er en stor fordel, specielt da der herved åbnes mulighed for anvendelse af et andet materiale end de organiske chlorholdige insekticider, hvilke insekticider er meget toxiske mod pattedyr og fugle, som det er velkendt. Et typisk eksempel på et sådant chlorholdigt insekticid er 1,4,5,6,7,8,8-heptachlor-3a,4,7,7a-tetrahydro-4,7-methanoinden, kendt under navnet heptachlor.However, as mentioned, 2,4-dimethyl-1,3-benzodioxol-4-yl-N-methylcarbamate has been found to be surprisingly useful in treating seeds to provide adequate protection in the soil for a sufficiently long period of time. This is a great advantage, especially since it allows for the use of a material other than the organic chlorine-containing insecticides, which insecticides are very toxic to mammals and birds, as is well known. A typical example of such a chlorine-containing insecticide is 1,4,5,6,7,8,8-heptachlor-3a, 4,7,7a-tetrahydro-4,7-methanoindene, known by the name of heptachlor.
Det fremgår af nedenstående forsøgsresultater, at ben-diocarb giver en større beskyttelse mod insektangreb end heptachlor ved samme eller lavere doseringsniveau. I de pågældende forsøg er der endvidere foretaget sammenligning med et kommercielt tilgængeligt carbamatinsekticid, nemlig 2,3-dihydro-2,2-dimethylbenzo-furan-7-yl-methylcarbamat, kendt under navnet carbofuran.It is evident from the following test results that ben-diocarb provides greater protection against insect infestation than heptachlor at the same or lower dosage level. In the experiments in question, a comparison is also made with a commercially available carbamate insecticide, namely 2,3-dihydro-2,2-dimethylbenzo-furan-7-yl-methylcarbamate, known by the name of carbofuran.
Ved forsøgene blev sukkerroefrø pelletteret med det pågældende insekticid i den anførte mængde, og frøene blev udsået på 8 forskellige lokaliteter i Tyskland til bestemmelse af antallet af planter, der spirede frem, hvilket antal afhænger af omfanget af insektangreb på frøene. I nedenstående tabel er anført antallet af fremkomne planter pr. meter sårække.In the experiments, beet pellets were pelleted with the insecticide in question in the amount indicated, and the seeds were sown at eight different sites in Germany to determine the number of plants that sprouted, which number depends on the extent of insect infestation on the seeds. The table below lists the number of plants obtained per year. meters of wounds.
4 1441414 144141
Forbindelse Kontrol Heptachlor Carbofuran Bendiocarb gram aktivt stof pr. 0 6,0 30,0 45,0 90,0 L50,0 3,0 6,0 12,0 __ 100.000 frø__________ 1 0,44 2,76 7,88 8,29 8,18 8,03 5,34 7,19 7,36 2 3,27 4,87 5,33 5,92 6,14 5,62 5,37 5,85 5,84 3 7,08 7,41. 7,07 7,17 6,68 6,36 6,88 7,33 7,19 tø β 4 2,78 6,45 6,87 7,43 6,83 5,68 7,01 6,37 7,13 o’ 5 0,46 2,07 5,496,24 6,13 6,20 4,135,63 5,87 3 6 6,72 6,98 6,75 7,15 7,04 6,68 6,71 7,02 7,31 I 7 1,49 2,87 3,57 2,52 3,73 3,30 2,39 2,38 3,13 a 8 6,94 7,20 7,08 7,44 6,95 6,91 7,02 7,10 7,17Compound Control Heptachlor Carbofuran Bendiocarb gram active substance per 0 6.0 30.0 45.0 90.0 L50.0 3.0 6.0 12.0 __ 100,000 seeds __________ 1 0.44 2.76 7.88 8.29 8.18 8.03 5.34 7.19 7.36 2 3.27 4.87 5.33 5.92 6.14 5.62 5.37 5.85 5.84 3 7.08 7.41. 7.07 7.17 6.68 6.36 6.88 7.33 7.19 tho 4 2.78 6.45 6.87 7.43 6.83 5.68 7.01 6.37 7, 13 o '5 0.46 2.07 5,496.24 6.13 6.20 4,135.63 5.87 3 6 6.72 6.98 6.75 7.15 7.04 6.68 6.71 7, 02 7.31 I 7 1.49 2.87 3.57 2.52 3.73 3.30 2.39 2.38 3.13 a 8 6.94 7.20 7.08 7.44 6.95 6.91 7.02 7.10 7.17
Gennsnsnit 3,65 5,08 6,26 6,52 6,46 6,10 5,60 6,11 6,41 % af kontrol 100 139 172 179 177 167 153 167 176Average 3.65 5.08 6.26 6.52 6.46 6.10 5.60 6.11 6.41% of control 100 139 172 179 177 167 153 167 176
Foruden bendiocarbs overlegenhed i forhold til heptachlor viser tabellen, at bendiocarb giver lignende resultater som carbofuran, men ved en dosering, som omtrent kun er en fjerdedel af hvad der kræves med carbofuran. Dette er meget overraskende, idet disse to carbamatinsecticider ved andre anvendelser end i jordbunden udviser praktisk taget samme insecticide aktivitet over for et bredt spektrum af insekter.In addition to bendiocarb's superiority to heptachlor, the table shows that bendiocarb yields similar results to carbofuran, but at a dosage of approximately one quarter of that required with carbofuran. This is very surprising, since these two carbamate insecticides exhibit practically the same insecticidal activity across a wide range of insects in applications other than the soil.
Bendiocarbs overlegenhed i jordbunden må derfor skyldes en helt uforudsigelig særlig stabilitet hos denne forbindelse.Bendiocarb's superiority in the soil must therefore be due to a completely unpredictable special stability of this compound.
Insekter, mod hvilke de omhandlede behandlede frø er beskyttede, omfatter biller og tovingede insekter, f.eks. smælderlarve (Agriotes Spp), pygmæbille (Atomaria), collembola og millipedes, symphilider og jordlopper (Chaetocnema Spp).Insects against which the treated treated seeds are protected include beetles and forcible insects, e.g. larvae (Agriotes Spp), pygmy beetle (Atomaria), collembola and millipedes, symphilids and earth fleas (Chaetocnema Spp).
Frømaterialet ifølge opfindelsen sås fortrinsvis således, at der opnås en carbamatkoncentration pr. hektar på fra 0,2 til 400 g på et område, som enten er inficeret med eller er udsat for infektion af de pågældende insekter. Koncentrationen af carbamat pr. hektar afhænger naturligvis i høj grad af, i hvilken mængde frøene sås, og dette afhænger af den pågældende afgrøde. Således er f.eks. en fore-trukken koncentration af carbamat, når de pågældende frø er sukkerroefrø, fra 1-15 g pr. hektar, medens der, i forbindelse med en kornafgrøde såsom hvede, foretrækkes en mængde på 200 g/hektar eller mere.The seed material of the invention is preferably sown so that one carbamate concentration per hectares ranging from 0.2 to 400 g in an area that is either infected with or susceptible to infection by the insects concerned. The concentration of carbamate per per hectare, of course, depends to a large extent on the amount of seeds sown, and this depends on the crop concerned. Thus, e.g. a preferred concentration of carbamate when the seeds in question are beet seeds, from 1-15 g per per hectare, in the case of a cereal crop such as wheat, an amount of 200 g / hectare or more is preferred.
144141 5144141 5
Det behandlede frømateriale ifølge opfindelsen kan foruden carbamatet indeholde andre aktive insekticider eller fungicider. Særligt egnede er blandinger med fungicider, f.eks. thiram, ben-quinox, captan eller S-ethyl-N-(3-dimethylaminopropyl)-thiocarbamat eller salte deraf, f.eks. hydrochlorid.In addition to the carbamate, the treated seed material of the invention may contain other active insecticides or fungicides. Particularly suitable are mixtures with fungicides, e.g. thiram, benquinox, captan or S-ethyl-N- (3-dimethylaminopropyl) thiocarbamate or salts thereof, e.g. hydrochloride.
Et yderligere insekticid kan også tilføres jorden, sædvanligvis i form af et granulat, på det tidspunkt, hvor man sår frømaterialet ifølge opfindelsen. Eksempler på sådanne insekticider er aldicarb, carbofuran, phorat, disulfoton, dimethoat, chlormephos, fonofos, diazinon, hexachlorcyclohexan, S-t-butylthio-methyl-0,0-diethyl-dithiophosphat og 3,3-dimethyl-l-methylthio-2-butanon-O-(methylcarbamoyl)oxim. 2,2-Dimethyl-l,3-benzodioxol-4-yl-N-methylcarbamat kan også tilføres til jorden.A further insecticide may also be applied to the soil, usually in the form of a granulate, at the time of sowing the seed material of the invention. Examples of such insecticides are aldicarb, carbofuran, phorate, disulfoton, dimethoate, chloromephos, phonophos, diazinone, hexachlorocyclohexane, St-butylthiomethyl-0,0-diethyldithiophosphate and 3,3-dimethyl-1-methylthio-2-butanone. -O- (methylcarbamoyl) oxime. 2,2-Dimethyl-1,3-benzodioxol-4-yl-N-methylcarbamate may also be added to the soil.
Opfindelsen illustreres nærmere ved hjælp af følgende eksempler .The invention is further illustrated by the following examples.
Eksempel 1Example 1
Sukkerroefrø blev behandlet ved pelletering efter Maribo-processen (Zucker, _2j5 (10), 533-540 (1973)). 2,2- Dimethyl-1, 3-benzodioxol-4-yl-N-methylcarbamat blev inkorporeret i pellete-ringsmidlet til opnåelse af en slutkoncentration på 10 g/kg ubehandlet frø.Beetroot seeds were processed by pelletizing after the Maribo process (Zucker, _2j5 (10), 533-540 (1973)). 2,2-Dimethyl-1,3-benzodioxol-4-yl-N-methylcarbamate was incorporated into the pelleting agent to give a final concentration of 10 g / kg of untreated seed.
Eksempel 2 Kålfrø blev behandlet .som følger: 2 kg Kålfrø blev anbragt i en metaltromle,og 20 g af et behandlingsmiddel med følgende sammensætning blev tilsat: 2,2-dimethy1-1,3-benzodioxol-4-yl-N- methylcarbamat 2,5 vægti attapulgitler 15 " "Risellan-olie 17 4 "Berkbond" nr. 1 (fyldmateriale på silikatbasis) 78,5 "Example 2 Cabbage seeds were treated as follows: 2 kg Cabbage seeds were placed in a metal drum and 20 g of a treating agent of the following composition was added: 2,2-dimethyl-1,3-benzodioxol-4-yl-N-methylcarbamate 2 , 5 wt. Attapulgitler 15 "" Risellan oil 17 4 "Berkbond" No. 1 (silicate-based filler) 78.5 "
Den lukkede tromle blev roteret på vandrette valser i 30 minutter til opnåelse af en jævn behandling af frømaterialet.The closed drum was rotated on horizontal rollers for 30 minutes to obtain an even treatment of the seed material.
Eksempel 3Example 3
Hvede blev behandlet på følgende måde: 6 14/4141 10 kg Hvede blev anbragt i en metaltromle,og 50 g af et behandlingsmiddel med følgende sammensætning blev tilsat: 2,2-dimethyl-l,3-benzodioxol-4-yl-N- methylcarbamat 10 vægt% attapulgitler 15 " "Ri$ellan-olie 17 4 "Berkbond" nr. 1 71Wheat was treated as follows: 6 14/4141 10 kg Wheat was placed in a metal drum and 50 g of a treating agent of the following composition was added: 2,2-dimethyl-1,3-benzodioxol-4-yl-N- methyl carbamate 10% by weight Attapulgitler 15 "" Ri $ ellan oil 17 4 "Berkbond" No. 1 71
Den lukkede tromle blev roteret på vandrette valser i 30 minutter til opnåelse af en jævn behandling af frømaterialet.The closed drum was rotated on horizontal rollers for 30 minutes to obtain an even treatment of the seed material.
Eksempel 4Example 4
Fem områder blev sået med lige store mængder (svarende til ca. 3 kg pelleteret frømateriale pr. hektar) pelleterede sukkerroefrø o Ved hvert område blev særskilte arealer sået med kontrolpellets ikke indeholdende 2,2-dimethyl-l,3-benzodioxol-4-yl-N-methylcarbamat og med pellets indeholdende carbamatet. De carbamat-holdige pellets gav ved såningen carbamatkoncentrationer på 3,0, 6,0 og 12,0 g/ha.Five areas were sown with equal amounts (corresponding to about 3 kg of pelleted seed material per hectare) of beet seed pelleted o At each area, separate areas were sown with control pellets not containing 2,2-dimethyl-1,3-benzodioxol-4-yl. -N-methylcarbamate and with pellets containing the carbamate. The carbamate-containing pellets yielded carbamate concentrations of 3.0, 6.0 and 12.0 g / ha at sowing.
Nedenstående tabel viser de gennemsnitlige antal fremkommende spirer pr. meter sået række:The table below shows the average number of emergent sprouts per day. meter sown row:
Tabel 1Table 1
Område Kontrol 3,0 g/ha 6,0 g/ha 12,0 g/ha (0 g/ha aktiv aktiv be- aktiv be- aktiv be~ bestanddel) standdel standdel standdel 1 0,44 5,34 7,19 ' 7,36 2 3,27 5,37 5,85 5,84 .3 2,78 7,01 6,37 7,13 4 0,46 4,13 5,63 5,87 5 1,49 2,39 2,38 3,13Area Control 3.0 g / ha 6.0 g / ha 12.0 g / ha (0 g / ha active active active active active ingredient) stand stand stand stand 1 0.44 5.34 7.19 7.36 2 3.27 5.37 5.85 5.84 .3 2.78 7.01 6.37 7.13 4 0.46 4.13 5.63 5.87 5 1.49 2, 39 2.38 3.13
Eksempel 5Example 5
Arealer på et enkelt område blev tilsået med lige store mængder af sukkerroefrø blandet omhyggeligt med henholdsvis 2,2-dimethyl~l,3-benzodioxol-4-yl-N-methylcarbamat (8 g/kg frø), γ-isomeren af 1,2,3,4,5,6-hexachlorcyclohexan (10 g/kg frø), og di-ethyl-3,5,6-trichlorpyridyl-phosphorothioat (10 g/kg frø).Areas in a single range were sown with equal amounts of sugar beet seeds mixed thoroughly with 2,2-dimethyl-1,3-benzodioxol-4-yl-N-methylcarbamate (8 g / kg seed), the γ isomer of 1, respectively. 2,3,4,5,6-hexachlorocyclohexane (10 g / kg seeds), and diethyl 3,5,5-trichloropyridyl phosphorothioate (10 g / kg seeds).
Antallet af blivende planter pr. hektar for disse tre arealer var henholdsvis 67.900, 46.500 og 39.600.The number of plants per year. hectares for these three areas were 67,900, 46,500 and 39,600 respectively.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8267/75A GB1519596A (en) | 1975-02-27 | 1975-02-27 | Dressing of seeds |
GB826775 | 1975-02-27 |
Publications (3)
Publication Number | Publication Date |
---|---|
DK81176A DK81176A (en) | 1976-08-28 |
DK144141B true DK144141B (en) | 1981-12-21 |
DK144141C DK144141C (en) | 1982-06-07 |
Family
ID=9849220
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DK81176A DK144141C (en) | 1975-02-27 | 1976-02-26 | FROEMATERIAL TREATED WITH INSECTICID |
Country Status (15)
Country | Link |
---|---|
AT (1) | AT349264B (en) |
BE (1) | BE838805A (en) |
CA (1) | CA1082942A (en) |
CS (1) | CS184792B2 (en) |
DD (1) | DD125546A5 (en) |
DE (1) | DE2607785A1 (en) |
DK (1) | DK144141C (en) |
FR (1) | FR2302040A1 (en) |
GB (1) | GB1519596A (en) |
GR (1) | GR60027B (en) |
IT (1) | IT1055924B (en) |
NL (1) | NL7601597A (en) |
SE (1) | SE420376B (en) |
TR (1) | TR18825A (en) |
ZA (1) | ZA761126B (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1555474A (en) * | 1975-08-14 | 1979-11-14 | Fisons Ltd | Pesticidal composition and method of compatingpests |
DE3442318A1 (en) * | 1984-11-20 | 1986-05-22 | VEB Schwermaschinenbau-Kombinat "Ernst Thälmann" Magdeburg, DDR 3011 Magdeburg | Process for application of agrochemicals in coating substances during seed pelletisation |
EP3696188A1 (en) | 2019-02-18 | 2020-08-19 | KWS SAAT SE & Co. KGaA | Gene for resistance to plant disease |
CN113646326A (en) | 2019-02-18 | 2021-11-12 | 科沃施种子欧洲股份两合公司 | Gene for resisting plant diseases |
EP3957168A1 (en) | 2020-08-17 | 2022-02-23 | KWS SAAT SE & Co. KGaA | Plant resistance gene and means for its identification |
-
1975
- 1975-02-27 GB GB8267/75A patent/GB1519596A/en not_active Expired
-
1976
- 1976-02-14 GR GR50054A patent/GR60027B/en unknown
- 1976-02-16 SE SE7601721A patent/SE420376B/en unknown
- 1976-02-17 NL NL7601597A patent/NL7601597A/en not_active Application Discontinuation
- 1976-02-19 TR TR18825A patent/TR18825A/en unknown
- 1976-02-20 BE BE164523A patent/BE838805A/en unknown
- 1976-02-23 AT AT125376A patent/AT349264B/en not_active IP Right Cessation
- 1976-02-25 CS CS7600001229A patent/CS184792B2/en unknown
- 1976-02-25 DD DD191476A patent/DD125546A5/xx unknown
- 1976-02-25 ZA ZA761126A patent/ZA761126B/en unknown
- 1976-02-26 DK DK81176A patent/DK144141C/en active
- 1976-02-26 IT IT7620605A patent/IT1055924B/en active
- 1976-02-26 DE DE19762607785 patent/DE2607785A1/en not_active Withdrawn
- 1976-02-26 CA CA246,636A patent/CA1082942A/en not_active Expired
- 1976-02-26 FR FR7605388A patent/FR2302040A1/en active Granted
Also Published As
Publication number | Publication date |
---|---|
CS184792B2 (en) | 1978-09-15 |
ZA761126B (en) | 1977-02-23 |
BE838805A (en) | 1976-08-20 |
FR2302040B1 (en) | 1979-08-24 |
DE2607785A1 (en) | 1976-09-09 |
DK81176A (en) | 1976-08-28 |
GR60027B (en) | 1978-03-31 |
IT1055924B (en) | 1982-01-11 |
ATA125376A (en) | 1978-08-15 |
CA1082942A (en) | 1980-08-05 |
FR2302040A1 (en) | 1976-09-24 |
DK144141C (en) | 1982-06-07 |
AT349264B (en) | 1979-03-26 |
SE7601721L (en) | 1976-08-30 |
AU1144376A (en) | 1977-09-01 |
DD125546A5 (en) | 1977-05-04 |
TR18825A (en) | 1977-11-01 |
NL7601597A (en) | 1976-08-31 |
SE420376B (en) | 1981-10-05 |
GB1519596A (en) | 1978-08-02 |
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