• Title/Summary/Keyword: 벼멸구에 대한 살충활성

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Insecticidal Activities and Repellent Effects of Plant Extracts against the Brown Planthopper (Nilaparvata lugens Stäl) (벼멸구에 대한 식물추출물의 살충활성과 기피효과)

  • Kim, Yeon-Kook;Lee, Jong-Jin;Choi, Man-Young
    • Korean journal of applied entomology
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    • v.47 no.1
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    • pp.65-74
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    • 2008
  • Methanol extracts of 35 plant species in 20 families were tested for their insecticidal activities and repellent effects against Nilaparvata lugens female adult by topical application and spray methods. The insecticidal activities and repellent effects of variousplant species and parts were different. The methanol extracts from stem of Garcinia xanthochymus, Senecio scandens and Phytolacca americana, seedcoat of Ginkgo biloba, and leaf+stem of Ailanthus altissima and Catalpa ovata showed potent insecticidal activities against N. lugens. Specially, the G. biloba extract exhibited higher than 90% mortality against N. lugens at a concentration of 4,000 ppm. Repellent effects of plant extracts obtained from whole plant of Daucus carota, fruit of Semecarpus anacardium, leaf+stem of C. ovata and Wisteria sinensis were active, and potent. Also, the plant extracts that are potent in insecticidal activity not necessarily have high repellent activity showing no significant corelation between the two activities.

Insecticidal and Acaricidal Activities of African Plant Extracts against the Brown Planthopper and Two-Spotted Spider Mite (아프리카산 식물체 추출물의 벼멸구 및 점박이응애에 대한 살충 및 살비활성)

  • I. G. Hiremath;Young Joon Ahn;Soon Il Kim;Byung Ryul Choi;Jum Rae Cho
    • Korean journal of applied entomology
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    • v.34 no.3
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    • pp.200-205
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    • 1995
  • Total 31 samples from 21 African plant species in 13 families were tested for their insecticidal and acaricidal activities against Nilaparvata lugens (Stal) and Tetranychus urticae (Koch) adults through topical application an leaf-dipping methods, respectively. The insecticidal and acaricidal activities were both plant parts and species dependent. The methanol extracts from whole plants of Casia occidental is and Cassia tora (Caesalpinaceae), an stem of Prosopis chinensis (Mimosaceae) revealed potent insecticidal activity against N. lugens. Potnet acaricidal activity against T. urticae was obtained from the methanol extracts from whole plants of Celosia trigyna (Amaranthaceae) and Combretum micronthum (Combretaceeae), leaves of Combretm glutinotum, and leaves and fruits of prosopis chinensis.

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Repellent and Insecticidal Activity of Sequential Extracting Fractions Obtained from BPH-Resistant Rice Varieties against Brown Planthopper (Nilaparvata lugens) (벼멸구 저항성벼 품종 추출분획물의 기피 및 살충 활성)

  • Kim, Sung-Eun;Kim, Young-Doo;Kim, Bo-Kyoung;Ko, Jae-Kwon;Chun, Jae-Chul
    • The Korean Journal of Pesticide Science
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    • v.10 no.2
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    • pp.124-130
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    • 2006
  • Rice plant extracts of brown planthopper (BPH) resistant rice varieties, Jangseongbyeo (JSB) and Hwacheongbyeo (HCB) at different growth stages (seedling, tillering, heading and ripening) were sequentially fractioned using hexane, ethyl ether, ethyl acetate, butanol, and distilled water. The extracts were applied to BPH susceptible rice variety, Dongjjnbyeo (DJB), to investigate the insecticidal and repellent effects against BPH. BPH insecticidal effects were not clearly observed with almost all of the extract fractions obtained from both JSB and HCB varieties for 12 h, whereas the ethyl ether and hexane extract fractions showed about 10 to 30% of BPH mortality in 24 to 48 h of application periods. An effective BPH repellent activity was found with the applications of ethyl ether extract fractions obtained from JSB variety. The extract fractions obtained from HCB variety did not show any different repellence among the various fractions. The BPH repellent effects of the extract fractions obtained at different growth stages of either JSB or HCB varieties did not show any correlations. The effect of ethyl ether fraction on BPH repellent was continually increased by 30 h after treatment and thereafter decreased. In addition, the first sub-fraction separated by a flash column chromatography eluted with chloroform:methanol (9:1, v/v) from the BPH effective ethyl ether faction in JSB variety might be meaningful to repel BPH from BPH susceptible target rice plants. The results indicated that the ethyl ether fraction obtained from JSB was higher in repellent activity than in insecticidal activity, and suggesting that there might be specific substance(s) in the first sub-fraction (sF1) of the ethyl ether fraction in JSB that could provide repellent activity against BPH.

Bioactivities of Korean Ginkgo (Ginkgo biloba L.) Extract and Its Potential as a Natural Pesticide (은행나무 추출물의 생물활성 및 천연물농약으로 이용 가능성)

  • Lee, Hyang-Burm;Kim, Han-Nah;Kim, Mi-Kyung;Kim, Chang-Jin;Kwon, Oh-Sung
    • Research in Plant Disease
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    • v.9 no.2
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    • pp.99-103
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    • 2003
  • Bioactivities of Korean ginkgo (Ginkgo biloba L.) extract were investigated against several fungi, general bacteria and insect pests. Crude methanolic extracts of different parts of Korean ginkgo showed different bioactivities depending on the target organisms. The methanolic extract showed in vitro antimicrobial activity at dose of 200 ug per paper disc. The extract of ginkgo stalk was some higher than seed coat and root. The extract also showed a remarkable in vivo antifungal activity against green mold (Trichoderma harzianum) on compost surface of spawn bags and in vivo insecticidal activity to Nilaparvata lugens, Plutella xylostella and Tetranychus urticae. This study suggests that Korean ginkgo extracts have a potential as a natural pesticide.

Insecticidal and Acaricidal Activities of Plant Extracts (식물체 추출물의 살충 및 살비활성)

  • Kwon, Min;Lee, Seong-Baek;Ahn, Young-Joon;Park, No-Jung;Cho, Kwang-Yun
    • Applied Biological Chemistry
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    • v.37 no.6
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    • pp.492-497
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    • 1994
  • Extracts of 43 species of plants were tested for their insecticidal and acaricidal activities against six species of insect pests and one mite species. The methanol extract of Ginkgo biloba leaves selectively was found to have potent insecticidal activity against Nilaparvata lugens (Stal), whereas steam distillate of Thujopsis dolabarata var. hondai sawdust showed potent insecticidal activities with a broad spectrum. The methanol extract of Pinus densiflora leaves and steam distillate of T. dolabrata var. hondai sawdust exhibited potent activities against Tetranychus urticae (Koch).

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Synthesis and biological activities of Chloronicotinyl derivatives (Chloronicotinyl 유도체의 합성 및 생물활성 검정)

  • Park, Su-Jin;Kim, In-Hae;Choi, In-Young;Kim, Song-Mun;Han, Dae-Sung;Hur, Jang-Hyun
    • The Korean Journal of Pesticide Science
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    • v.3 no.1
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    • pp.20-28
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    • 1999
  • Chloronicotinyl derivatives were synthesized by substitution of amino in 3-pyridylmethylamine with phosphite groups and their insecticidal and fungicidal activities were determined. At 500 ppm, compound 4 with methyl and butyl group in phosphonate and compound 5, 6, 7, and 8 with two butyl, 2,2,2-trifluorotehtyl, 2-ethylhexyl, phenyl, respectively, in phosphonate showed 90% insecticidal activities against brown plant-hopper (Nilaparvate lugens). These compounds showed, however, poor insecticidal activities against diamond-back moth (Plutella xylostella) and two-spotted spider mite (Tetranychus urticae) (<65%), suggesting that insecticidal activity of chloronicotinyl derivatives containing phosphorus moieties are species-dependent. Newly synthesized chloronicotinyl derivatives with halogen and/or heterocycle (compound $10{\sim}21$) did not show insecticidal activities. We also determined fungicidal activity of the synthesized chloronicotinyl derivatives against rice sheath blight (Pyricularia grisea), cucumber gray mold (Bortytis cinerea), tomato late blight (Phytophthora infestans), wheat leaf rust (Puccinia recondita), and barley powdery mildew (Erysiphe graminis). Compound 10 with butyl and 4-nitrophenyl in phosphonate at 10 ppm showed 85% fungicidal activity against rice blast, suggesting that chloronicotinyl derivatives containing phosphorus moieties could be developed as a fungicidal agent of a novel chemical structure.

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3D-QSAR Analysis on the Insecticidal Activities of N-Substituents on Imidazol Ring in Imidacloprid Analogues (Imidacloprid 유도체 중 imidazol 고리상 N-치환체들의 살충활성에 대한 3D-QSAR 분석)

  • Soung, Min-Gyu;Kim, Se-Gon;Soog, Nack-Do
    • The Korean Journal of Pesticide Science
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    • v.11 no.3
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    • pp.131-137
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    • 2007
  • CoMFA and CoMSIA model were derived and reviewed on the insecticidal activities of N-substituents (X) on the imidazol ring in imidacloprid analogues at the different alignment condition. Regarding the predictability ($q^2$ or $r_{cv.}^2$) and fitness ($r_{ncv.}^2$) of the two optimized models, the atom based fit (A) alignments were better than that of the field fit (F) alignment and, on the other hand, CoMSIA (A10) model was better than CoMFA (A5) model. Also, from the most optimized CoMSIA (A10) model, the insecticidal activity by N-substituents (X) was dependence on the electrostatic field and H-bond acceptor field. It is predicted that, from the contour maps with optimized CoMSIA (A10) model, H-bond acceptors at ortho- and meta- position will contribute for improving of insecticidal activities and, as the functional groups of carbonyl oxygen atom are charged negatively and positively charged at the ortho- position of benzyl group, insecticidal activities will also be improved.

Comparison of Insecticidal Activity and Feeding Behavior of Nilaparvata lugens by Root Uptake Times against Fenobucarb and Imidacloprid (Fenobucarb와 Imidacloprid의 벼 뿌리 침지시간에 따른 벼멸구의 살충활성과 섭식행동비교)

  • Yang, Jeong-Oh;Cho, Sun-Ran;Kwon, Yun-Hee;Yoon, Chang-Mann;Kim, Gil-Hah
    • The Korean Journal of Pesticide Science
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    • v.14 no.2
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    • pp.175-182
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    • 2010
  • Two insecticides, fenobucarb (36, 12 ppm) and imidacloprid (0.7, 0.4 ppm) were treated on rice seedling roots by root uptake method with different dipping time (1, 4, 8, 12, 16, 20, 24 hrs). This study was performed to elucidate the correlation between insecticidal activity and feeding behavior of Nilaparvata lugens using EPG (electrical penetration graph). EPG waveforms are recorded for 4 hours and classified into six waveforms. In the correlation between root uptake and corrected mortality, both insecticides showed higher corrected mortality as higher doses and as longer root uptake times. In the analysis of waveforms, N. lugens showed longer nonprobe time but shorter phloem feeding time at a higher dose. It was also showed the same result as longer the root uptake times. Therefore, it showed the correlation between insecticidal activity by root uptake time and both EPG waveforms (non-probing time and phloem feeding time).

Insecticidal activity of the crude extract and its fractions of Custard apple (Annona reticulata L.) (커스타드애플(Annona reticulata L.)씨 추출물과 그 분획물의 살충활성)

  • Shin, Suk-Hyun;Choi, Geun-Hyoung;Choi, Dal-Sun;Kwon, Oh-Kyung;Im, Geon-Jae;Park, Jae-Up;Choi, Byung-Ryul;Kim, Tae-Wan;Kim, Jin-Hyo
    • Journal of Applied Biological Chemistry
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    • v.53 no.1
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    • pp.21-24
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    • 2010
  • In recent years, many agricultural scientists are studying on eco-friendly farming methods. Among of lots of the methods, the natural insecticides are highly motivated and interested due to their safety and biodegradable issues, and readily available source of bioinsecticides. In this study, the crude extract of custard apple (Annona reticulata L.) seed and its three fractions which were separated based on polarity indexes were examined for their insecticidal activities against Myzus persicae Sulzer and Nilaparvata lugens S.. The crude extract (Aceton/MeOH) showed strong insecticidal activities against both insects at 3.00 mg/mL ($LD_{50}$=0.45mg/mL for M. persicae S. and 1.42 mg/mL for N. lugens S.). Furthermore, simple fractionation with hexane, chloroform, and water lead to increase three-folds insecticidal activity on chloroform fraction ($LD_{50}$=0.13mg/mL for M. persicae S. and 1.14 mg/mL for N. lugens S.). The results suggest that A. reticulata extracts might be used to control for M. persicae effectively.