PL75865B2 - - Google Patents
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- PL75865B2 PL75865B2 PL15683472A PL15683472A PL75865B2 PL 75865 B2 PL75865 B2 PL 75865B2 PL 15683472 A PL15683472 A PL 15683472A PL 15683472 A PL15683472 A PL 15683472A PL 75865 B2 PL75865 B2 PL 75865B2
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- urea
- weight
- dimethylurea
- chlorophenyl
- salts
- Prior art date
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- 239000002917 insecticide Substances 0.000 claims description 11
- 239000004202 carbamide Substances 0.000 claims description 8
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 6
- 239000004009 herbicide Substances 0.000 claims description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 3
- YBSLUBPQYDULIZ-UHFFFAOYSA-N oxalic acid;urea Chemical compound NC(N)=O.OC(=O)C(O)=O YBSLUBPQYDULIZ-UHFFFAOYSA-N 0.000 claims description 3
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 3
- 235000011164 potassium chloride Nutrition 0.000 claims description 3
- 239000001103 potassium chloride Substances 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 230000002363 herbicidal effect Effects 0.000 claims description 2
- 150000002696 manganese Chemical class 0.000 claims description 2
- 235000007079 manganese sulphate Nutrition 0.000 claims description 2
- 239000011702 manganese sulphate Substances 0.000 claims description 2
- SQQMAOCOWKFBNP-UHFFFAOYSA-L manganese(II) sulfate Chemical compound [Mn+2].[O-]S([O-])(=O)=O SQQMAOCOWKFBNP-UHFFFAOYSA-L 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 239000011780 sodium chloride Substances 0.000 claims description 2
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims 1
- IVUXTESCPZUGJC-UHFFFAOYSA-N chloroxuron Chemical compound C1=CC(NC(=O)N(C)C)=CC=C1OC1=CC=C(Cl)C=C1 IVUXTESCPZUGJC-UHFFFAOYSA-N 0.000 claims 1
- 230000003647 oxidation Effects 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 9
- 241000238631 Hexapoda Species 0.000 description 8
- 241001465754 Metazoa Species 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 230000003204 osmotic effect Effects 0.000 description 5
- 231100000614 poison Toxicity 0.000 description 4
- 241000607479 Yersinia pestis Species 0.000 description 3
- 230000009931 harmful effect Effects 0.000 description 3
- 230000004060 metabolic process Effects 0.000 description 3
- 231100000252 nontoxic Toxicity 0.000 description 3
- 230000003000 nontoxic effect Effects 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 239000002574 poison Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 2
- 235000011613 Pinus brutia Nutrition 0.000 description 2
- 241000018646 Pinus brutia Species 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 150000002823 nitrates Chemical class 0.000 description 2
- 150000002826 nitrites Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 231100000572 poisoning Toxicity 0.000 description 2
- 230000000607 poisoning effect Effects 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- 240000005020 Acaciella glauca Species 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 239000005949 Malathion Substances 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 235000008582 Pinus sylvestris Nutrition 0.000 description 1
- 241000245665 Taraxacum Species 0.000 description 1
- 235000005187 Taraxacum officinale ssp. officinale Nutrition 0.000 description 1
- 241001271990 Tomicus piniperda Species 0.000 description 1
- CRPUJAZIXJMDBK-UHFFFAOYSA-N Toxaphene Natural products C1CC2C(=C)C(C)(C)C1C2 CRPUJAZIXJMDBK-UHFFFAOYSA-N 0.000 description 1
- FSAVDKDHPDSCTO-WQLSENKSSA-N [(z)-2-chloro-1-(2,4-dichlorophenyl)ethenyl] diethyl phosphate Chemical compound CCOP(=O)(OCC)O\C(=C/Cl)C1=CC=C(Cl)C=C1Cl FSAVDKDHPDSCTO-WQLSENKSSA-N 0.000 description 1
- VYWQTJWGWLKBQA-UHFFFAOYSA-N [amino(hydroxy)methylidene]azanium;chloride Chemical compound Cl.NC(N)=O VYWQTJWGWLKBQA-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000005667 attractant Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000005786 degenerative changes Effects 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 1
- JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000000763 evoking effect Effects 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 229960000453 malathion Drugs 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- -1 manganese salts Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- QHDUJTCUPWHNPK-UHFFFAOYSA-N methyl 7-methoxy-2h-indazole-3-carboxylate Chemical compound COC1=CC=CC2=C(C(=O)OC)NN=C21 QHDUJTCUPWHNPK-UHFFFAOYSA-N 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- OEJNXTAZZBRGDN-UHFFFAOYSA-N toxaphene Chemical compound ClC1C(Cl)C2(Cl)C(CCl)(CCl)C(=C)C1(Cl)C2(Cl)Cl OEJNXTAZZBRGDN-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
Pierwszenstwo: Zgloszenie ogloszono: 30.05.1973 Opis patentowy opublikowano: 15.01.1975 75865 W- 451/ 9/02 MKP A01n 9/02 Twórcawynalazku: Jan Kulesza Uprawniony z patentu tymczasowego: Instytut Badawczy Lesnictwa, Warszawa (Polska) Srodek owadobójczy Przedmiotem wynalazku jest nietoksyczny srodek owadobójczy, stanowiacy roztwór wodny herbicydów mocznikowych, mocznika i jego soli oraz soli manganu i chlorków potasowców.Dotychczasowe metody chemicznej ochrony roslin polegaly prawie wylacznie na stosowaniu pestycy* dów-trucizn politoksycznych o malej selektywnosci dzialania.Wszystkie syntetyczne insektycydy, sluzace do zwalczania szkodliwych owadów, zarówno chlorowane weglowodory (DDT, HCH, aldrin, toksafen itp.) jak tez zwiazki fosforoorganiczne (systoks, paration/malation, foschlor, DDVP, chlorofenwinfos, fenitrotion) czy tez pochodne kwasu karbominowego (sewin, unden) dezakty- wuja bardzo silnie okreslone enzymy w organizmach wszystkich zwierzat, nie tylko owadów.W organizmach wiekszych zwierzat i u ludzi nie wystepuja na ogól trwale zatrucia, lecz tylko pewne przemijajace symptomy podraznien nerwowych. Przy czestym stykaniu sie z insektycydami niekiidy nastepuje ich kumulacja w tkankach, co powoduje trwale zmiany degeneracyjne centrów nerwowych. Nieostrozne postepo¬ wanie z niektórymi insektycydami jak np. z DDT doprowadzilo do takiego rozpowszechnienia tej trucizny w sro¬ dowiskach zycia, ze znajduje sie ja w miesie zwierzat, w rybach, w wodzie morskiej, mleku, jajkach ptaków itp.Spowodowalo to odwrót od trwalych insektycydów. • - -" Stosowane równiez do zwalczania owadów zwiazki fosforoorganiczne i karbaminiany, sa na ogól mniej trwale, a produkty ich rozkladu nie kumuluja sie w tkankach zwierzecych. Wiekszosc tych zwiazków charakte¬ ryzuje sie jednak wysoka toksycznoscia dorazna, a nawet stwierdzono teragogenne dzialanie niektórych z nich.W zwiazku z tym poszukiwane sa bardziej bezpieczne srodki zwalczania szkodników przez stosowanie np. srod¬ ków odstraszajacych (repellentów) lub wywolujacych sterylizacje plciowa owadów (chemosterylanty) albo przynecajacych do zatrutych miejsc zerowania (atraktanty), oraz przez stosowanie trucizn pokarmowych. Poszu¬ kiwania te dotychczas nie daly pozytywnych wyników.Dla unikniecia szkodliwego wplywu insektycydów na otoczenie postawiono sobie za cel opracowanie srodka owadobójczego nietoksycznego.Cel ten osiagnieto na drodze badan nad znalezieniem metod podwyzszania naturalnej odpornosci roslin na ataki szkodników i pasozytów przez stosowanie zwiazków chemicznych czynnych fizjologicznie, wywolujacych2 76 865 •zybkie i doic glebokie zmiany w metabolizmie roslin, zaklócajace mozliwosc normalnego odzywiania owadów, a w nastepstwie ich zniszczenie, przy czym szczególna uwage zwrócono na te zwiazki azotu, które wywoluja w roslinach szybkie zmiany cisnienia osmotycznego. Najszybsze zmiany w metabolizmie roslin wywoluja zwiazki chemiczne sluzace do niszczenia roslin, a wiec wszelkiego, rodzaju herbicydy, które w malych stezeniach maja równiez wlasciwosci aktywizacji wzrostu roslin.Nietoksyczny srodek owadobójczy wedlug wynalazku usuwa calkowicie grozbe zatrucia srodowiska i zwie¬ rzat pozytecznych. Polega ona na stosowaniu lacznym do zwalczania szkodliwych owadów nietrujacych zwiaz¬ ków chemicznych, które sa zdolne wywolywac szybkie zmiany biochemizmu roslin i cisnienia osmotycznego w tkankach tych roslin. Jednym z latwiej dostepnych wskazników wlasciwej drogi postepowania sa wyniki pomiarów cisnienia osmotycznego i szybkosc zmian wjednym z obranych kierunków metabolizmu: azotowym, weglowodanowym lub fosforowym. Najlepsze wyniki otrzymano stosujac zwiazki chemiczne wywolujace przyspieszenie nagromadzenia azotynów i azotanów i w iglach sosny pospolitej (mocznik, azotan mocznika, szczawian mocznika, chlorowodorek mocznika), zmniejszenie zawartosci cukrów redukcyjnych {herbicydy mocz¬ nikowe) oraz zwiekszajace w igliwiu zawartosc kwasów organicznych (mieszanina soli manganu i chlorków pota- sowców). Mocznik i jego pochodne powoduja duze skoki cisnienia osmotycznego w traktowanych roslinach.Stwierdzono, ze silnym dzialaniem niszczacym zerujace gasienice szkodliwych owadów, takich jak bar¬ czatka sosnówka, brudnica mniszka, borecznik sosnowy, osnuja gwiazdzista odznacza sie uzywany w ilosci 20 do 30 kg na 1 hektar chronionego drzewostanu, roztwór wodny 10—20% mieszaniny, o skladzie 30% wagowych herbicydu mocznikowego, zwlaszcza N-^-chlorofenylu^N^-dwumetylomocznika lub N-(4-chlorofenylo- ^hT-metylo-NMzobutinylo-mocznika, lub 3-(4-(4-cldorofenoksy)-fenylo)-l,l-dwumetylomocznika lub N-cyklo- oktylo-N\N*-dwumetylomocznika, lub N-^bromofenylo^N^metylo-N^metoksy-mocznika, 40% wagowych szczawianu mocznika, 20% wagowych siarczanu manganu i 10% wagowych chlorku sodu. Roztwór ten jest dosc szybko absorbowany przez igly sosny i juz po uplywie 24 godzin nastepuje wzrost cisnienia osmotycznego w tkankach o 100 do 300% oraz wzrost zawartosci azotynów i azotanów a takze kwasów organicznych o 50 do 200%. Oprócz tego nastepuje przejsciowy spadek zawartosci cukrów o 50 do 60%. Wywolane zmiany trwaja zwykle 8 do 14 dni, nastepnie wszystko wraca do normy za wyjatkiem zawartosci kwasów organicznych, która utrzymuje sie w iglach na wysokim poziomie jeszcze w ciagu okolo jednego roku. Po uplywie 3 do 4 godzin od wykonania oprysku roztworem srodka owadobójczego gasienice owadów przestaja zerowac a po uplywie 4 do 5 dni opadaja martwe. PLPriority: Application announced: May 30, 1973 The patent description was published: January 15, 1975 75865 W- 451 / 9/02 MKP A01n 9/02 Inventor: Jan Kulesza Authorized by the provisional patent: Forest Research Institute, Warsaw (Poland) Insecticide The subject of the invention is a non-toxic insecticide, which is a water solution of urea herbicides, urea and its salts as well as manganese salts and potassium chloride. Until now methods of chemical plant protection consisted almost exclusively of the use of pesticides * polytoxic poisons with low selectivity of action. All synthetic insecticides used to combat harmful insects, both chlorinated hydrocarbons (DDT, HCH, aldrin, toxaphene, etc.) as well as organophosphorus compounds (systox, parathion / malathion, phosphine, DDVP, chlorfenvinphos, phenitrothione) or derivatives of carbomic acid (sevine, undene) very strongly disactivate certain enzymes in the body of all animals, not only insects In animals and humans, there are generally no permanent poisoning, but only some transient symptoms of nervous irritation. Frequent contact with nonkiidy insecticides causes their accumulation in tissues, which causes permanent degenerative changes in nerve centers. Careless handling of some insecticides, such as DDT, has led to such a widespread use of this poison in the habitats of life that it is found in the meat of animals, fish, sea water, milk, bird eggs, etc., and this has resulted in a retreat from permanent insecticides. • - - "Organophosphates and carbamates, also used to control insects, are generally less persistent, and their decomposition products do not accumulate in animal tissues. Most of these compounds are, however, highly toxic, and some of them have even been found to be teragogenic. Therefore, safer pest control agents are sought by the use of, for example, repellants or agents that induce sex sterilization of insects (chemosteroids) or attracting to poisoned zero sites (attractants), and by the use of food poisons. These nods have so far not yielded positive results. In order to avoid the harmful effects of insecticides on the environment, the goal was to develop a non-toxic insecticide. This goal was achieved through research on finding methods to increase the natural resistance of plants to attacks by pests and parasites by the use of active compounds physiologically, evoking 2 76 865 • profound changes in plant metabolism, interfering with the normal nutrition of insects, and subsequent destruction, with particular attention being paid to those nitrogen compounds that cause rapid changes in plant osmotic pressure. The fastest changes in plant metabolism evoke chemical compounds used to destroy plants, i.e. all kinds of herbicides, which in low concentrations also have the properties of activating plant growth. According to the invention, the non-toxic insecticide completely eliminates the risk of environmental poisoning and beneficial animals. It is based on the combined use of non-poisonous chemical compounds to combat insect pests, which are capable of inducing rapid changes in plant biochemistry and osmotic pressure in plant tissues. One of the more easily available indicators of the right course of action are the results of measurements of osmotic pressure and the rate of changes in one of the chosen directions of metabolism: nitrogen, carbohydrate or phosphorus. The best results were obtained with the use of chemical compounds accelerating the accumulation of nitrites and nitrates in Scots pine needles (urea, urea nitrate, urea oxalate, urea hydrochloride), reducing the content of reducing sugars (urea herbicides) and increasing the content of organic acids in the needles (a mixture of manganese salts) and potassium chloride). Urea and its derivatives cause large spikes in osmotic pressure in the treated plants. It has been found that they have a strong destructive effect on the null caterpillars of harmful insects such as pine beetle, dandelion moth, pine borwort, stellate envelope is used at a rate of 20 to 30 kg per 1 hectare of protected forest stand, an aqueous solution of 10-20% of a mixture consisting of 30% by weight of urea herbicide, especially N - 4 - chlorophenyl - N - dimethyl urea or N - (4-chlorophenyl - 4HT-methyl-NMzobutinyl-urea, or 3 - (4- (4-cldorophenoxy) phenyl) -1,1-dimethylurea or N-cyclooctyl-N \ N * -dimethylurea, or N- 4-bromophenyl-N-methyl-N-methoxyurea, 40% by weight of urea oxalate, 20% by weight of manganese sulphate and 10% by weight of sodium chloride This solution is quickly absorbed by pine needles and after 24 hours the osmotic pressure in the tissues increases by 100 to 300% and the content of nitrites and nitrates as well as organic acids by 50 d by 200%. In addition, there is a temporary decrease in the sugar content of 50 to 60%. The induced changes usually last 8 to 14 days, then everything returns to normal, except for the organic acid content, which remains high in the needles for about a year. After 3 to 4 hours from the spraying with the insecticide solution, the insect caterpillars stop netting and after 4 to 5 days they fall dead. PL
Claims (1)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL15683472A PL75865B2 (en) | 1972-07-20 | 1972-07-20 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL15683472A PL75865B2 (en) | 1972-07-20 | 1972-07-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL75865B2 true PL75865B2 (en) | 1974-12-31 |
Family
ID=19959443
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL15683472A PL75865B2 (en) | 1972-07-20 | 1972-07-20 |
Country Status (1)
| Country | Link |
|---|---|
| PL (1) | PL75865B2 (en) |
-
1972
- 1972-07-20 PL PL15683472A patent/PL75865B2/pl unknown
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