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1.
Pest Manag Sci ; 69(12): 1379-84, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23423954

RESUMO

BACKGROUND: Plants can rapidly evolve resistance to herbicide in response to repeated selection. This study focuses on cross-resistance patterns observed in Lolium rigidum following pyroxasulfone recurrent selection. RESULTS: The parental MR (multiresistant) population following four generations of pyroxasulfone recurrent selection evolved cross-resistance to prosulfocarb and triallate. At the recommended label rate of prosulfocarb or triallate (2000 g ha(-1) ), the progeny selected four times with pyroxasulfone (MR4) displayed 58 and 35% plant survival respectively. One additional cycle of prosulfocarb selection increased the resistance level to both prosulfocarb and triallate in the population MR4-P1. Prosulfocarb resistance is yet to be reported in L. rigidum field populations. CONCLUSIONS: This study suggests that L. rigidum plants can rapidly evolve cross-resistance to several wheat-selective herbicides under recurrent selection of a single mode of action. Weed populations displaying broad-spectrum cross-resistance to several herbicide modes of action are increasing in frequency in intensive world agriculture. Proactive and integrated measures for resistance management need to be developed globally on appropriate herbicide use in crop rotations.


Assuntos
Carbamatos/farmacologia , Resistência a Herbicidas , Herbicidas/farmacologia , Isoxazóis/farmacologia , Lolium/efeitos dos fármacos , Plantas Daninhas/efeitos dos fármacos , Sulfonas/farmacologia , Trialato/farmacologia , Controle de Plantas Daninhas
2.
J Hered ; 93(1): 48-50, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12011175

RESUMO

Extensive use of the preemergence herbicide triallate over the last three decades has selected for resistant (R) Avena fatua L. populations in several areas of the United States and Canada. R plants are also cross-resistant to the unrelated pyrazolium herbicide difenzoquat. We made reciprocal crosses between inbred R and susceptible (S) lines to determine the genetic basis of triallate resistance. Seeds from parental lines and F(2) populations were treated with soil applications of 0.275, 0.55, or 1.1 kg/ha triallate in the greenhouse and plant heights recorded after 37 days. Surviving F(2) plants were selfed and the resulting F(3) families were screened with 1.1 kg/ha triallate. In the F(2) populations, assortment of S and R phenotypes fit a 15:1 segregation ratio, suggesting that resistance was controlled by the two independently segregating recessive genes TRR1 and TRR2. None of the 912 F(3) progeny from 51 R F(2) individuals was susceptible to triallate treatment, further supporting a two-gene mode of inheritance. There was a possible maternal effect on susceptibility at the highest triallate rate tested.


Assuntos
Avena/genética , Resistência a Medicamentos/genética , Genes Recessivos , Herbicidas/farmacologia , Trialato/farmacologia , Avena/efeitos dos fármacos , Cruzamentos Genéticos , Genes de Plantas , Pirazóis/metabolismo
4.
Cancer Res ; 38(1): 13-5, 1978 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-201368

RESUMO

In an investigation of the mutagenic properties of 20 carbamate herbicides and fungicides by use of the Salmonella/microsome mutagenicity test as developed by Ames et al. (Mutation Res., 31: 347-364, 1975), we have found that three thiocarbamate compounds, diallate, sulfallate and triallate, are mutagenic in the presence of a liver microsomal fraction on strains TA1535 and TA100. This indicates that the metabolic products of these thiocarbamates are causing base-pair substitutions. Since the 2-chloro-allyl group is common to the three mutagenic compounds but is not common to the 17 nonmutagenic compounds, a metabolic derivative of this group is probably responsible for the mutagenic activity.


Assuntos
Fungicidas Industriais/farmacologia , Herbicidas/farmacologia , Mutagênicos , Tiocarbamatos/farmacologia , Trialato/farmacologia , Animais , Ditiocarb/análogos & derivados , Avaliação Pré-Clínica de Medicamentos , Técnicas In Vitro , Microssomos Hepáticos/metabolismo , Ratos , Salmonella typhimurium/efeitos dos fármacos , Relação Estrutura-Atividade
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