• Title/Summary/Keyword: bispyribac-sodium

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Herbicidal Efficacy of Bispyribac-sodium Combined with Other Herbicides for Annual Bluegrass(Poa annua L.) Suppression (새포아풀(Poa annua L.) 방제를 위한 Bispyribac-sodium과 타약제와의 혼합 상호작용)

  • Park, Nam-Il;Lee, In-Yong;Park, Jae-Eup;Kim, Ho-Jun;Chun, Jae-Chul;Ogasawara, Masaru
    • Asian Journal of Turfgrass Science
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    • v.21 no.1
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    • pp.39-49
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    • 2007
  • Bispyribac-sodium is a new-type herbicide that prevents the occurrence of annual bluegrass by the suppression of anthesis and inflorescence emergence on the bent green. The greenhouse experiment was conducted to investigate interaction effect of the bispyribac-sodium with 21 soil- and foliar-applied herbicides in regards of herbicidal activity of annual bluegrass. The remarkable synergism was not found on the combination of bispyribac-sodium with benfluralin, pendimethalin, oryzalin, siduron, chlorphtalim, isoxaben, bifenox, tenylchlor, indanofan, bentazone, imazosulfuron, imazaquin, halosulfuron-methyl and limsulfuron. However, mixture of bispyribac-sodium with mecoprop, triclopyr, metsulfuron-methyl, cyclosulfamuron, pyrazosulfuron-ethyl and pyributicarb produced greater synergism of herbicidal activity when compared with unmixed, single application. Phytotoxicity was low on bentgrass green and fast recovery was observed. In future, it would be strongly necessary to do research to Investigate the effect of bispyribac-sodium combination with other herbicides under various environment and management practices on-site bentgrass green.

Control of Annual Bluegrass(Poa annua L.) by Bispyribac-sodium (Bispyribac-sodium 처리에 의한 새포아풀(Poa annua L.) 방제)

  • Park, Nam-Il;Lee, In-Yong;Park, Jae-Eup;Kim, Ho-Jun;Chun, Jae-Chul;Ogasawara, Masaru
    • Asian Journal of Turfgrass Science
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    • v.20 no.2
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    • pp.157-165
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    • 2006
  • This study was initiated to investigate herbicidal selectivity margin with annual bluegrass and bentgrass according to growth stages through herbicidal spectrum of bispyribac-sodium and therefore to examine application possibility to prevent annual bluegrass selectively. The herbicidal efncacy by pre-emergence application was generally low. But a high herbicidal efficacy was observed over 90% for Shehpherd's purse. Foliar treatment resulted in a higher herbicidal efficacy in all tested plants except dallisgrass, lovegrass, curled dock and bentgrass as compared with pre-emergence application. We found bispyribac-sodium could be used as a selective weeding chemical between annual bluegrass and bentgrass. In regard to dose-responses to the growth stage, annual bluegrass was more susceptible to bispyribac-sodium than bentgrass for the same dosage. Particularly, bispyribac-sodium application in inflorescence emergence stage showed a greater herbicidal selectivity margin of 6.8 times with annual bluegrass over creeping bentgrass after 28 days from the application. These data demonstrated that annual bluegrass was more sensitive to bispyribac-sodium over creeping bentgrass.

In vitro Metabolism of Pyribenzoxim

  • Kim, Ki Young;Kim, Jin;Liu, Kwang Hyeon;Lee, Hye-Suk;Kim, Jeong-Han
    • Journal of Applied Biological Chemistry
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    • v.43 no.1
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    • pp.49-53
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    • 2000
  • The in vitro metabolism of a new herbicide pyribenzoxim, {benzophenone O-[2,6-bis[(4,6-dimethoxy-2-pyrimidinyl)oxy]benzoyl]oxime} was studied using rice, barnyardgrass and rat liver microsomes. No metabolism of pyribenzoxim was observed with rice and barnyardgrass microsomes though the cvtochrome P450 was active, which was evidenced by the metabolism of cinnamic acid. With rat liver microsomes, four metabolites (M1, M2, M3, and M4) were produced while parent compound decreased. M1 and M2 were from the hydrolysis reactions and NADPH-dependent metabolites were M3 and M4 (major metabolite) which were hydroxylated by cytochrome P450. They were identified as bispyribac-sodium (M1), benzophenone oxime (M2), {benzophenone O-[2,6-bis[(5-hydroxy-4,6-dimethoxy-2-pyrimidinyl)oxy]-benzoyl]oxime}(M3), and {benzophenone O-[2[(5-hydroxy-4,6-dimethoxy-2l-pyrimidinyl)6-(4,.6dimethoxy-2-pyrimidinyl)oxy]benzoyl]oxime} (M4) through LC/MS/MS analyses. Based on the results obtained metabolic map of pyribenzoxim is proposed.

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