• Title/Summary/Keyword: Chemical insecticide

검색결과 160건 처리시간 0.025초

해충의 살충제저항성과 금후대책 (Insect Pest Resistance to Insecticides and Future Researches)

  • 최승윤
    • 한국응용곤충학회지
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    • 제22권2호
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    • pp.98-105
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    • 1983
  • The rapid increase in cases of insect resistance to insecticides indicates that the contribution of present chemical control practices inevitably leads to exhaustion of available insecticide resources against key insect species. Now the problem of insecticide resistance exists worldwide among insects and mites affecting field crops and animals including human beings, ranging from minimal or absent in some developing countries, where use of insecticides has been low, to extremely severe in many developed countries. Since the occurrence of insect resistance to insecticides was firstly recognized in 1908, the increase in recent decades has been almost linear and now the number of species of insects and acarines in which resistant strains have evolved have been increased to a total of 432. Of these, $261(60\%)$ are agricultural importance and $171(40\%)$ of medical/veterinary importance. The phenomenon of insecticide resistance is asserting itself as the greatest challenge to effective chemical control of many important insect pests. Resistance of insects to insecticides has a history of nearly 80 years, but its greatest increase and its strongest impact have occurred during the last 40 years following the discovery and extensive use of synthetic organic insecticides and acaricides. The impact of resistance should be considered not only in terms of greater cost of pest control due to increased dosages and number of applications but also in terms of the ecological disruption of pest-beneficial species density relationships, the loss of investment in the development of the insecticides concerned, and socio-economic disruption in agricultural communities. Despite its grave economic consequences, the phenomenon of insecticide resistance has received surprisingly little attention in Korea. Since the study of insecticides started firstly in 1963, many entomologists have been concerned with this study. According to their results, some of the rice pests and some of the mites on orchard trees, for example, have developed worrisome level of resistance in several areas of this peninsula. With many arthropods, considerable advances in the developed countries have been made in the study of the biochemical and physiological mechanisms of resistance. Progress involves the biochemical characteristics of specific defense mechanisms, their genetics, interactions, and their quantitative and qualitative contribution to resistance. But their studies arc still inadequately known and relatively little have been contributed in terms of unique schemes of population management in achieving satisfactory pest control. It is apparent that there is no easy solution to resistance as a general phenomenon. For future challenging to effective control of insect pests which are resistant to the insecticides concerned, new insecticide groups with distinctly novel mode of action are urgently needed. It is clear, however, that a great understanding of the factors which govern the intensity of selection of field population for resistance could lead to far more permanently successive use of chemicals within the framework of integrated pest management than heretofore practiced.

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유도체화 반응에 의한 현미 중 thiosultap의 분석 (Analysis of Thiosultap in Hulled Rice by Derivatization)

  • 최정희;도정아;윤혜정;박용춘;김재훈;최동미
    • 농약과학회지
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    • 제14권1호
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    • pp.16-20
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    • 2010
  • Thiosultap은 중국에서 사용되고 있는 nereistoxin계 살충제로 국내에는 등록되지 않아 중국산 농산물 수입시 잔류 농약 안전관리를 위한 시험법 마련이 시급한 실정이다. 이에 본 연구에서는 현미 중 thiosultap을 염기조건에서 nereistoxin으로 유도체화하여 GC-FPD로 분석하는 시험법을 개발하였다. 산염기 분배를 이용한 정제 조건을 확립하였으며, 확립된 시험법에 의한 정량한계와 직선성을 측정한 결과 각각 0.05 mg $kg^{-1}$과 0.995$(r^2)$이었다. 무처리 현미에 thiosultap 0.5와 2.5 mg $kg^{-1}$을 처리하여 회수율을 측정한 결과는 $96.1{\pm}7.9\sim100.8{\pm}6.1%$로 양호한 결과를 나타내었다.

Structural Investigation of Bistrifluron Using X-Ray Crystallography, NMR Spectroscopy, and Molecular Modeling

  • Moon, Joon-Kwan;Kim, Jeong-Han;Rhee, Sang-Kee;Kim, Gang-Beom;Yun, Ho-Seop;Chung, Bong-Jin;Lee, Sang-San;Lim, Yoong-Ho
    • Bulletin of the Korean Chemical Society
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    • 제23권11호
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    • pp.1545-1547
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    • 2002
  • A new insecticide, bistrifluron acts as an inhibitor of insect development and interferes with the cuticle formation of insects. Since it shows low acute oral and dermal toxicities, it can be one of potent insecticides. Based on X-ray crystallography, NMR spectroscopy and molecular modeling, the structural studies of bistrifluron have been carried out.

Syntheses of 3-Pyrimidyl- and 3-Pyranyl-5,6-benzocoumarin Derivatives

  • El-Deen, Ibrahim M.;Al-Wakeel, El-Sayed I.;El-Mawla, Ahmed G.
    • Bulletin of the Korean Chemical Society
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    • 제23권4호
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    • pp.610-612
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    • 2002
  • A competitive enzyme-linked immunosorbent assay (ELISA) was developed for the quantitative detection of organophosphorus insecticide cyanophos. An analogue (hapten) of cyanophos was synthesized and was coupled to BSA to produce polyclonal antibodi es from rabbits. The antisera were screened against another hapten coupled to ovalbumin (OVA). Using the sera of highest specificity, an antigen-coated ELISA was developed, which showed an I50 of 310 ng/mL with the detection limit of 20 ng/mL. The antibodies showed negligible cross-reactivities with other organophosphorus pesticides except for parathion-methyl, which makes the assay suitable for the selective detection of cyanophos.

유기인계 살충제 (다이아지논)에 대한 물벼룩, Daphnia magna (Cladocera: Daphniidae) 개체군의 공간분산 변이 (Change in Spatial Dispersion of Daphnia magna(Cladocera: Daphniidae) Populations Exposed to Organophosphorus Insecticide, Diazinon)

  • 이상희;지창우;전태수
    • Environmental Analysis Health and Toxicology
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    • 제24권3호
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    • pp.231-240
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    • 2009
  • We explored collective behaviors of indicator species to elucidate the effect of the chemical stress. After the treatments of an insecticide, diazinon, at low concentrations (1.0 and 10.0 ${\mu}g/L$), spatial dispersion patterns of Daphnia magna were checked in a test chamber. The I-index was used to characterize the movement data before (0~1 h) and after (1~2 h) the treatments in laboratory conditions. The slopes of the frequency distribution of I-index in semi-log scale decreased significantly, and the test populations appeared to be more dispersed with a lower degree of aggregation after the treatments. The index was feasible in indicating decrease in the ability of the specimens to keep desirable distances with neighbor individuals under chemical stress and showed a possibility of monitoring presence of toxic chemicals in environment through group behavior measurement.

Chemical Compositions and Insecticidal Activity of Eucalyptus urophylla Essential oil Against Culex quinquefasciatus Mosquito

  • Pujiarti, Rini;Kasmudjo, Kasmudjo
    • Journal of the Korean Wood Science and Technology
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    • 제44권4호
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    • pp.494-504
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    • 2016
  • Eucalyptus oils are widely used as spices, perfume industrial materials, food flavorings, and medicines. Several types of Eucalyptus oils also have insecticidal activity and as carminative. This study investigated the chemical composition, insecticidal (larvicidal and repellent) activity of E. urophylla oil against filarial mosquito Culex quinquefasciatus. E. urophylla oil was obtained from fresh leaves by water-steam distillation with oil yield 1.08%. E. urophylla oil in this study had no color (clear), has odor (typical eucalyptus), with specific gravity 0.941; refractive index 1.465; miscibility in 70% ethanol 1 : 3; and optical rotation (-) $5.83^{\circ}$. The major compounds of the oil were ${\alpha}$-pinene (11.73%), 1,8-cineole (49.86%), ${\beta}$-ocimene (6.25%), ${\gamma}$-terpinene (9.11%), and ${\alpha}$-terpinyl acetate (7.63%). The result showed the excellent insecticide activity against C. quinquefasciatus. The oil provided larvicidal activity with $LC_{50}$: 80.21 ppm and $LC_{90}$: 210.18 ppm, and repellent activity with $IC_{50}$: 0.82% and $IC_{90}$: 4.88%. The present study showed the effectiveness of E. urophylla as natural insecticide against C. quinquefasciatus, the mosquito vector of filariasis.

2,2-bis(2-methoxy-5-chlorophenyl) 1,1,1-trichloroethane의 合成 과 殺蟲能에 관하여 (Synthesis and Insecticidal effects of 2,2-bis(2-methoxy-5-chlorophenyl) 1,1,1-trichloroethane)

  • 이대수;김재항;최달형;최영연
    • 대한화학회지
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    • 제10권4호
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    • pp.149-152
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    • 1966
  • 鹽素置換 anisol과 chloral hydrate를 縮合하면 D.D.T 類의 合成에서와 같이 bis compound의 化合物이 生成될 것이고 D.D.T 系統의 化合物처럼 殺蟲能이 있으리라고 豫測되므로 4-chloro anisol 과 chloral hydrate를 縮合하여 生成物의 構造를 檢討하였던 바 2,2 bis(2-methoxy-5-chlorophenyl) 1.1.1-trichloroethane임을 確認하였으며 反應條件과 「국화꼬마수염진딧물」 및 「귤응애」에 대한 殺충能을 檢討한 結果 前報文$^{(67)}$에서 發表한 바 있는 化合物들의 殺蟲能에 比하여 5培나 强한 殺蟲能을 가졌다는 事實을 알았다.

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5.7-Dibromo-8-hydroxyquinolinyl-N-ethylcarbamate의 합성및 항균작용에 관한 연구 (Study on the synthesis and Antimicrobial activity of 5.7-Dibromo-8-hydroxyquinolinyl-N-ethylcarbamate)

  • 강회양;민경진
    • 한국환경보건학회지
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    • 제22권1호
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    • pp.21-27
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    • 1996
  • 5.7-Dibromo-8-hydroxyquinolinyl-N-ethylcarbamate, one of the carbamate derivative which are generally used as insecticide, was newly synthesized. Its physical properities were determined and chemical structure was identified by means of I.R., nmr in addition to elemental analysis. The yield of addition, using triethylamine as catalyst, 5.7-dibromo-8-hydroxyquinoline and isocyanate was better than that of condensation of 5.7-dibromo-8-hydroxyquinoline with carbamoylchloride. The present organic synthesized compound showed the bacteriostatic action on salmonella typhi, escherichia coli and pseudomonas aeruginosa, but no otherwise effect of contraction of rabbit's ileum in the concentration of $100 \mu g/ml$.

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Carbamate 화합물의 합성 및 위생학적 연구 (Synthesis and Biological Activities of Carbamate Derivative)

  • 강회양
    • 한국환경보건학회지
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    • 제22권2호
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    • pp.19-24
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    • 1996
  • Carbamates are generally used as insecticide, thus 5.7-dichloro-8~hydroxyquinolinyl- N-ethylcarbamate was newly synthesized. Its physical properties were determined and chemical structure was identified by means of I.R., nmr in addition to elemental analysis. The yield of addition, using triethylamine as catalyst, 5.7-dichloro-8-hydroxyquinoline and isocyanate was better than that of condensation of 5.7-dichloro-8-hydroxyquinoline with carbamoylchloride. The effct of the compound on rabbit's ileum, and antibacterial activity against Staphylococcus aureus, Salmonella typhi, Echerichia coli, and Pseudomonas aeruginosa were examined. The present organic synthesized compound showed the bacteriostatic action on salmonella typhi, escherichia coli, and pseudomonas aeruginosa, but no otherwise effect of contraction of rabbit's ileum in the concentration of $250 \mu g/ml$.

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5.7-Dichloro-8-hydroxyquinaldyl-N-ethylcarbamate의 합성 및 항균작용에 관한 연구 (Study on the Synthesis and Antimicrobial Activity of 5.7-Dichloro-8-HydroxyquinaldyI-N-Ethylcarbamate)

  • 강회양
    • 한국환경보건학회지
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    • 제24권1호
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    • pp.47-53
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    • 1998
  • 5.7-Dichloro-8-hydroxyquinaldyl-N-ethylcarbamate, one of the carbamate derivative which are generally used as insecticide, was newly synthesized. Its physical properities were determined and chemical structure was indentified by means of I.R., nmr in addition to elemental analysis. The yield of addition, using triethylamine as catalyst, 5.7-dichloro-8-hydroxyquinaldine and isocyanate was better than that of condensation of 5.7-dichloro-8- hydroxyquinaldine with carbamoylchloride. The effect of the cornpond on rabbit's ileum, and antibacterial activity against Staphylococcus aureus, Salmonella typhi, Escherichia coli, and Pseudomonas aeruginosa were examined. It was observed that the dosage over 100 $\mu$g/ml of the compound relaxed rabbit's ileum and the same dosage of the compound inhibited growth of the above strains of bactera.

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