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Dive into the research topics where P. Gaillardon is active.

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Featured researches published by P. Gaillardon.


Pesticide Biochemistry and Physiology | 1987

Effect of the cytochrome P-450 inactivator 1-aminobenzotriazole on the metabolism of chlortoluron andisoproturon in wheat☆

F. Cabanne; D. Huby; P. Gaillardon; René Scalla; F. Durst

Abstract Roots of young wheat plants ( Triticum aestivum cv Clement) were treated with [ 14 C]chlortoluron or [ 14 C]isoproturon alone or mixed with 1-aminobenzotriazole (ABT), a mechanism-based inactivator of cytochrome P -450 monooxygenases. Radioactivity extracted from shoots slightly decreased during periods of metabolism, this decrease being reduced by ABT in the case of isoproturon. ABT strongly inhibited the metabolism of both herbicides. Accumulation of metabolites was generally depressed in the presence of ABT; however, levels of the free N -monodemethylated derivatives were little or not affected. It is concluded that ABT is a synergist of chlortoluron and isoproturon in wheat because it inhibits the enzymes responsible for the ring-alkyl hydroxylation of chlortoluron and putatively of isoproturon, as well as the second N -demethylation of isoproturon. The possibility that those enzymes belong to the class of cytochrome P -450 monooxygenases is discussed.


Pesticide Biochemistry and Physiology | 1985

Phytotoxicity and metabolism of chlortoluron in two wheat varieties

F. Cabanne; P. Gaillardon; René Scalla

Abstract Varietal susceptibility of winter wheat to chlortoluron, 1-(3-chloro-4-methylphenyl)-3,3 dimethylurea, has been studied in two varieties, Corin (susceptible) and Clement (tolerant). After a 24-hr root absorption of the herbicide, phytotoxicity was estimated from growth measurements. When administered at 12 to 96 μM concentrations, the herbicide reduced the growth of both varieties. A significant selective effect was found at 96 μM. Measurements of chlorophyll fluorescence-induction kinetics allowed to discriminate between the two varieties treated with 12 to 48 μM chlortoluron. The metabolism of chlortoluron was studied following absorption of 24 μM solutions. Both varieties produced the same pattern of metabolites but the tolerant variety degraded the herbicide and the phytotoxic mono-N-demethylated metabolite at a slightly higher rate. An unexpected result was that the more susceptible variety possessed a very significant ability to metabolize chlortoluron. In conclusion, it appears that further studies are necessary before deciding whether the differences in susceptibility of the two varieties can be explained by the only metabolic factor.


Weed Research | 1994

Changes in the concentrations of isoproturon and its degradation products in soil and soil solution during incubation at two temperatures

P. Gaillardon; M. Sabar


Weed Research | 1985

Effect of mixed function oxidase inhibitors on the toxicity of chlortoluron and isoproturon to wheat.

P. Gaillardon; F. Cabanne; R. Scalla; F. Durst


Weed Research | 1991

Effect of low temperatures on 2,4-D behaviour in maize plants

C. Gauvrit; P. Gaillardon


Weed Research | 1990

Differential toxicity of simazine and diuron to Torilis arvensis and Lolium rigidum

R. de Prado; René Scalla; P. Gaillardon


Weed Research | 1991

Study of diuron in soil solution by means of a novel simple technique using glass microfibre filters

P. Gaillardon; F. Fauconnet; P. Jamet; G. Soulas; R. Calvet


Weed Research | 1989

Interaction between diclofop-methyl and 2,4-D in wild oat (Avena fatua L.) and cultivated oat (Avena sativa L.), and fate of diclofop-methyl in cultivated oat

B. Kafiz; J. P. Caussanel; René Scalla; P. Gaillardon


Weed Research | 1980

Adsorption de quelques phénylurées herbicides par des acides humiques

P. Gaillardon; Raoul Calvet; J.C. Gaudry


Weed Research | 1977

Adsorption et désorption de la terbutryne par une montmorillonite-Ca et des acides humiques seuls ou en mélanges

P. Gaillardon; Raoul Calvet; M. Terce

Collaboration


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René Scalla

Institut national de la recherche agronomique

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F. Cabanne

Institut national de la recherche agronomique

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Raoul Calvet

Institut national de la recherche agronomique

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J.C. Gaudry

Institut national de la recherche agronomique

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B. Kafiz

Institut national de la recherche agronomique

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C. Gauvrit

Institut national de la recherche agronomique

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D. Huby

Institut national de la recherche agronomique

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F. Fauconnet

Institut national de la recherche agronomique

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G. Soulas

Institut national de la recherche agronomique

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J. P. Caussanel

Institut national de la recherche agronomique

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