• Title/Summary/Keyword: herbicidal selectivity

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Herbicidal Activity of Newly Rice Herbicide Tefuryltrione Mixture against Sulfonylurea Resistant Weeds in Korea (설포닐우레아계 제초제 저항성 논잡초에 대한 신규 제초제 Tefuryltrione 합제의 약효 및 선택성)

  • Park, Min-Sik;Kim, Se-Min;Park, Yong-Seog;Lee, Kun-Sik;Woo, Jung
    • Korean Journal of Weed Science
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    • v.32 no.2
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    • pp.133-138
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    • 2012
  • This study was conducted to investigate the herbicidal activity against resistant biotype on sulfonylurea (SU) herbicides such as Scirpus juncoides and Monochoria vaginalis at the glasshouse and paddy rice cultivation area. In order to investigate resistance breakability against SU-resistanted annual weeds, new rice herbicides containing tefuryltrione [p-hydrophenyl pyruvate dioxygenase (HPPD) inhibitor] were tested. In both lab test and field experiment, tefuryltrione mixture, 4-HPPD inhibitor had shown excellent efficacy with a bleaching on the leaves of resistant annual weeds at early time after treatment and showed excellent persistance. Especially, tefuryltrione mixture had shown excellent controlling effect on annual and perennial SU-resistant S. juncoides in the regional field experiment. In phytotoxicity test, this tefuryltrione mixture had shown good selectivity to common rice species.

Quantitative structure-activity relationships for the growth inhibition activity of the herbicidal 3-phenyl-5-(3,7-dichloro-8-quinolinyl)-1,2,4-oxadiazole derivatives (제초성 3-Phenyl-5-(3,7-dichloro-8-quinolinyl)-1,2,4-oxadiazole 유도체들의 정량적인 구조와 생장 저해 활성과의 관계)

  • Sung, Nack-Do;Lee, Sang-Ho;Kim, Hyoung-Rae;Song, Jong-Hwan
    • The Korean Journal of Pesticide Science
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    • v.6 no.4
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    • pp.279-286
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    • 2002
  • To improve the growth inhibition activities and selectivities for quinclorac family, novel 3-substituted phenyl-5-(3,7-dichloro-8-quinolinyl)-1,2,4-oxadiazole derivatives as the substrate were synthesized and their the activities ($pI_{50}$) against shoot and root of rice plant (Oryza sativa L.) and barn-yard grass (Echinochloa crus-galli) were measured. And the quantitative structure-activity relationships (QSARs) between physicochemical parameters of the substitutents (R) on phenyl group and the activities ($pI_{50}$) were analyzed quantitatively. According to the SAR analyses, the substrates of planar conformation showed higher herbicidal activities against barnyard grass than rice plant. The activities against rice plant depend on the electronic effect (shoots: ${\sigma}_{opt.}=0.49$ & root: $R_{opt.}=-0.15$) of substituents, whereas the activities against shoots and roots of barnyard grass depend on hydrophobicity (${\pi}_{opt.}=0.37{\sim}2.40$). There were conditions of selective growth inhibition activity against barnyard grass when such a ortho-substituted electron donating substituents showing the hydrophobicity value, ${\pi}=2.40$ were introduced on the phenyl ring. The 2-tolyl substituent predicted from SAR equations was expected to have better growth inhibition activity and selectivity (${\Delta}pI_{50}=1.26$) for barnyard grass.

Herbicidal Activity of d-Limonene to Burcucumber (Sciyos angulatus L.) with Potential as Natural Herbicide (천연물 유래 d-Limonene의 가시박 방제효과)

  • Choi, Jung-Sup;Ko, Young-Kwan;Cho, Nam-Gyu;Hwang, Ki-Hwan;Koo, Suk-Jin
    • Korean Journal of Weed Science
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    • v.32 no.3
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    • pp.263-272
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    • 2012
  • The potential as natural herbicide of d-limonene natural agent was conducted on several weeds in a greenhouse and Sciyos angulatus in field condition. Herbicidal activity of foliar application at a concentration of 100 and 200 kg ai $ha^{-1}$ of d-limonene on seven weed species was completely killed in a greenhouse condition. Also, d-limonene at a concentration of 50 kg ai $ha^{-1}$ was completely killing on Abutilon theophrasti, Aeschynomene indica, Echinochloa crus-galli and Digitaria ciliaris 3 days after treatment. While pre-emergence treatment of d-limonene concentration of 12.5 to 200 kg ai $ha^{-1}$ showed not significant visible damages. Phytotoxic symptoms of d-limonene by foliar treatment were characterized by wilting and burn-down of leaves and stems followed by discoloration, finally, plant death. Crop selectivity at d-limonene concentration of 100 kg ai $ha^{-1}$ over to five main crops including Zea mays by foliar application was not at all. Field trial of foliar treatment with d-limonene 70 to 140 kg ai $ha^{-1}$ have effectively controled over 5~20 leaf stages of S. angulatus at the natural habitats. And herbicidal efficacy of foliar application on S. angulatus with carrier volume in field condition was increased with dose dependent manners. These results suggest that d-limonene is considered possible as herbicide, and may be further optimized for natural agent for environmental friendly natural herbicide.

Herbicidal Activity of Herbicidin from a Strain of Soil Actinomycete Streptomyces scopuliridis (토양 방선균 유래 Herbicidin의 제초활성)

  • Won, Ok Jae;Kim, Young Tae;Kim, Jae Deok;Choi, Jung Sup;Ko, Young Kwan;Park, Kee Woong
    • Weed & Turfgrass Science
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    • v.4 no.3
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    • pp.219-224
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    • 2015
  • This study was conducted to evaluate the effect of herbicidin, new natural herbicidal substances, derived from soil actinomycetes Streptomyces scopuliridis. Several weed species were subjected to examine the germination inhibition and herbicidal activity at the concentration from 100 to 2,000 ppm. There was no selectivity in germination inhibition and herbicidal activity against crops. Germination of Echinochloa oryzoides, Digitaria ciliaris, Abutilon theophrasti and Amaranthus retroflexus was inhibited completely when 7.81 ppm of extract was treated in petri dish. Pre-emergence application of herbicidin in soil condition showed low inhibition against weeds. However, post application of herbicidin in green house resulted in the necrosis of weeds at the concentration of 2,000 ppm. A. retroflexus was sensitive to herbicidin at the low concentration of 62.5 ppm, whereas E. oryzoides was tolerant to lower concentration of herbicidin until it became withered at the concentration of 2,000 ppm. In conclusion, herbicidal substances derived from S. scopuliridis herbicidin, which is consisted with herbicidin A and B, have dominant effect on germination and growth inhibition. On the other hand, herbicidin was insufficient to control gramineous weeds. In future, it will be needed to develop the combination of herbicidin with other herbicide or compounds to control gramineous weeds as well.

Biological activities of novel quinolinyloxadiazoles (신규 quinolinyloxadiazole 유도체의 생물활성)

  • Hwang, In-Taek;Choi, Jung-Sub;Hong, Kyung-Sik;Lee, Byung-Hoe;Kim, Jin-Seog;Ryu, Eung-Kul;Cho, Kwang-Yun
    • The Korean Journal of Pesticide Science
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    • v.2 no.3
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    • pp.52-63
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    • 1998
  • A novel quinolineoxadiazoles, substituted the carboxylic acid group with 1,2,4-oxadiazole radicle, of KSC-16960 and related compounds were evaluated to examine the herbicidal activity, crop injury and residual effect of after-vegetable crops compared with those of quinclorac (3,7-dichloro-8-quinolinecarboxylic acid), of which use is now banned because of its residual activity to some succeeding vegetable crops. KSC-16960 showed 2- and 3-leaf stages of barnyardgrasses effectively controlled by more than 95 and 90%, respectively, at a rate of 6.25 g/ha. The dose of KSC-16960 controlled 4- and 5-leaf stages of barnyardgrasses by more than 90% were found to be 50 g and 100 g/ha, respectively. The selectivity of KSC-16960 between direct-seeded rice and barnyardgrass was approximately 2-fold higher than that of quinclorac when they were treated to the soil. The selectivity indices of KSC-16960 and of quinclorac between 1-leaf stage of direct seeded rice and 5-leaf stage of barnyardgrass were 44 and 23, respectively, and those between 1-leaf stage of direct seeded rice and 4-leaf stage of barnyardgrass were almost 2-fold higher. Application of KSC-16960 with bentazone exhibited an additive controlling effect on several weed species, but that of quinclorac exhibited an antagonistic effect. With pyrazosulfuron-ethyl, on the other hand, both application of KSC-16960 and quinclorac showed additive interactions. Under a greenhouse condition, the residual activity of KSC-16960 to succeeding tomato plants was approximately 4-fold lower compared to that of quinclorac. KSC-16960 could be substituted for quinclorac, if it will be made some more improvement for reducing residual activity.

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Herbicidal Effects and Crop Selectivity of Sorgoleone, a Sorghum Root Exudate under Greenhouse and Field Conditions (온실과 포장조건에서 수수 추출물 Sorgoleone의 제초활성 및 작물 선택성)

  • Uddin, Md. Romij;Won, Ok-Jae;Pyon, Jong-Yeong
    • Korean Journal of Weed Science
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    • v.30 no.4
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    • pp.412-420
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    • 2010
  • Weeds are known to cause enormous losses due to their interference in agro ecosystems. Because of environmental and human health concerns, worldwide efforts are being made to reduce the heavy reliance on synthetic herbicides that are used to control weeds. In this regard phytotoxicity of allelochemical sorgoleone, which is a major component of the hydrophobic root exudates of Sorghum bicolor was evaluated in different weed species and also its crop selectivity in greenhouse and field conditions. Sorgoleone strongly inhibited the growth of different weeds by pre-emergence and post-emergence applications both in greenhouse and field conditions. Post-emergence application of sorgoleone on 21-day-old weed seedlings had a greater inhibitory effect than the pre-emergence application. Again, broadleaf weed species were more susceptible than grass species to the application of sorgoleone at both stages of growth. Growth of broadleaf weed species was suppressed by greater than 80% for most of the weed species except a few species and among them the species Rumex japonicus and Galium spurium were completely suppressed at $200{\mu}g\;ml^{-1}$ sorgoleone. Like greenhouse trial, sorgoleone was more effective for broadleaf weed species followed by sedge and grass weed species in the field condition. The growth inhibition of weeds was slightly lower in field condition compared to greenhouse condition. The crop species like rice, barley, wheat, corn, perilla, tomato, soybean and Chinese cabbage were tolerant to sorgoleone while lettuce and cucumber were slightly susceptible to sorgoleone. Consequently, sorgoleone may be applied to control weeds in organic farms without affecting the growth of crop.

Absorption, Translocation and Metabolism of Bensulfuron in Rice and Weeds at Different Temperatures (벼와 잡초에서 온도조건(溫度條件)에 따른 Bensulfuron의 흡수(吸收), 이행(移行) 및 대사(代謝))

  • Kang, T.G.;Pyon, J.Y.
    • Korean Journal of Weed Science
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    • v.15 no.4
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    • pp.321-328
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    • 1995
  • Absorption, translocation, and metabolism study of $^{14}C$-bensulfuron were conducted to determine selectivity and herbicidal action of bensulfuron in two rice cultivars and three paddy weeds at different temperatures. 1. Absorption of $^{14}C$-bensulfuron was greater at 30/$25^{\circ}C$ than at 25/$20^{\circ}C$ and also in cv. Sangpung than in cv. Samgang, and Cyperus serotinus and Sagittaria pygmaea showed greater amount of absorption than Echinochloa crus-galli. 2. Translocation rate of bensulfuron was higher at 30/$25^{\circ}C$ than at 25/$20^{\circ}C$ and also in cv. Sangpung than in cv. Samgang, and C. serotinus showed highest translocation rate followed by the S. pygmaea and E. crus-galli. 3. In metabolism study, concentration of parent compound in rice plants was greater in cv. Sangpung which was susceptible to bensulfuron than in cv. Samgang. More amount of parent compound was distributed in shoots and root of C. serotinus and S. pygmaea than E. crus-galli. 4. It may suggested that sensitivity to bensulfuron between rice cultivars may be due to different inactivation metabolic ability and phytotoxicity of rice increased at high temperature since higher amount of bensulfuron was absorbed. Higher herbicidal activity of bensulfuron may caused by higher absorption and translocation in three weed species at high temperature.

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Comparative molecular field analysis (CoMFA) and holographic quantitative structure-activity relationship (HQSAR) on the growth inhibition activity of the herbicidal 3-phenyl-5-(3,7-dichloro-8-quinolinyl)-1,2,4-oxadiazole derivatives (제초성 3-Phenyl-5-(3,7-dichloro-8-quinolinyl)-1,2,4-oxadiazole 유도체들의 생장 저해활성에 관한 비교 분자장 분석 (CoMFA)과 분자 홀로그램 구조-활성관계 (HQSAR))

  • Sung, Nack-Do;Lee, Sang-Ho;Song, Jong-Hwan;Kim, Hyoung-Rae
    • The Korean Journal of Pesticide Science
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    • v.7 no.2
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    • pp.108-116
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    • 2003
  • A series of new quinclorac family, herbicidal 3-phenyl-5-(3,7-dichloro-8-quinolinyl)-1,2,4-oxadiazole derivatives as substrate were synthesized and their growth inhibition activity $(pI_{50})$ against root and shoot of rice plant (Oryza sativa L.) and barnyard grass (Echinochloa crus-galli) were determined. And then comparative molecular field analysis (CoMFA) and molecular holographic quantitative structure- activity relationship (HQSAR) were compared in terms of their potential for predictiability. The statistical results were suggested that HQSAR based model had better predictability than CoMFA model. The selective factors to remove barnyard grass take electron withdrawing groups which can be created positive charge and steric bulky on the phenyl ring. Results revealed that the unknown 2,6-dichloro-substituent, U5 and 2,4,6-trichloro-substituent, U6(${\Delta}pI_{50}$=CoMFA: 1.18 & HQSAR: 1.82) were predicted as compound with higher activity and selectivity.

A New Approach for Practical Classification of Herbicide and for Effective Use by Two-dimensional Ordination Analysis (Two-Dimensional Ordination 분석법에 의한 제초제살초 Spectrum 분류와 효과적인 사용법)

  • Kim Soon Chul
    • Korean journal of applied entomology
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    • v.22 no.2 s.55
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    • pp.147-159
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    • 1983
  • In general, herbicides have been classified according to selectivity, mobility. time of application, methods of application, mode of action and chemical property and structure. However, there was no generally accepted classification system for practical use in the field. The primary processes affected by the majority of herbicides are the growth process through cell elongation and/or cell division, the photosynthetic process specifically the light reaction, the oxidative phosphorylation and the integrity of the membrane systems. The usual approach in the study of the mechanism by which herbicides kill or inhibit the growth of plants is to initially determine the morphological phototoxicity systems, The mechanism by which a herbicide kills a plant or suppresses its development is actually the resultant effect of primary and secondary(or side) effects. In most instances, the death of the plant is due to the secondary effects. To induce the desired response, a herbicide must be able to gain entry into the plants and once inside, to be transported within the plant to its site(s) of activity in concentrations great enough. Obstacles to the entry and movement of herbicides in plants are generally classified by leaf and soil obstacles, translocation obstacles and biochemical obstacles, and these obstacles are also strongly influenced by plant species and by environmental factors such as light, temperature, rainfall and relative humidity. And hence, in most instances, results obtained from laboratory or greenhous vary from those of field experiment. Author attempted to classify herbicides from the field experiment using the two-dimensional ordination analysis to obtain practical information for selecting effective herbicides or to choose effective herbicide combinations for increasing herbicidal efficacy or reducing the chemical cost. Based on this two-dimensional diagram, desired herbicides or combinations were selected and further investigated for the interaction effects whether these combinations are synergistic, additive or antagonistic. From the results, it was concluded that these new approach could possibly be give more comprehensive informations about effective use of herbicide than any other systems.

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Herbicidal Activities and Crop Injury of Hairy Vetch Residues (헤어리벳치 잔류물이 제초활성 및 작물 약해에 미치는 영향)

  • Won, Ok-Jae;Uddin, Md Romij;Pyon, Jong-Yeong
    • Korean Journal of Weed Science
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    • v.31 no.2
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    • pp.175-182
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    • 2011
  • This study was conducted to evaluate the growth inhibition of weeds and selectivity of crop species by hairy vetch residues. The growth of all the weed species was suppressed greater than 90% at the ratio 60 : 40 of hairy vetch residues and no weeds were emerged at 90 : 10 mixture in the greenhouse. It was noticed that broadleaf weed species were more suppressed compared to grass weed species. Growth of weeds was significantly reduced and the inhibition percent was increased with increasing application depths of hairy vetch mixture both in vinylhouse and in field conditions. Among the different application depths of hairy vetch mixture, 0.75 cm depth of application tended to inhibit more, but statistically no significant difference was observed between 0.5 cm and 0.75 cm application depth. The growth of weed species such as Galium spurium, Chenopodium album, Plantago asiatica, and Rumex japonicus was greatly suppressed in the vinylhouse and the growth of G. spurium, R. japonicus and Amaranthus retroflexus was suppressed significantly in the field condition. The growth inhibition of all the above mentioned sensitive weed species was approximately 80% at the application depth of 0.5 cm. Crop growth was not hampered by using the residues of hairy vetch. This study demonstrated that rotation crop residues of hairy vetch contained high allelopathic potential to different weed species without hampering the growth of crop species.