Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Donald G. Rusness"'
Publikováno v:
Pesticide Biochemistry and Physiology. 61:115-133
Quinclorac and 13 synthesized esters were monitored for toxicity in foliar- and soil-treated leafy spurge plants. Foliar treatment at 0.5 μmol/plant with quinclorac resulted with 100% mortality, whereas treatment with esters at 2 μmol/plant showed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61437e59cc39e4be1249bcb5c26f1abd
https://doi.org/10.1006/pest.1998.2357
https://doi.org/10.1006/pest.1998.2357
Autor:
Donald G. Rusness, Gerald L. Lamoureux
Publikováno v:
Pesticide Biochemistry and Physiology. 42:128-139
BAS 145 138 (1-dichloroacetylhexahydro-3,3,8α-trimethylpyrrolo[1,2-α]pyrimidin-6-(2 H -one)) protected corn from injury due to low levels of chlorimuron ethyl ( N -[4-chloro-6-methoxy-pyrimidin-2-yl]- N′ -[2-ethoxycarbonylbenzenesulfonyl]urea). I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9eb4f74636c96778c46aded173dc7754
https://doi.org/10.1016/0048-3575(92)90060-d
https://doi.org/10.1016/0048-3575(92)90060-d
Autor:
Donald G. Rusness, Gerald L. Lamoureux
Publikováno v:
Zeitschrift für Naturforschung C. 46:882-886
BAS 145138 was moderately effective in protecting corn from injury due to chlorimuron ethyl. BAS 145138 increased the I50 of chlorimuron ethyl to corn, determined by root-growth in a sandy loam soil, from 6 g chlorimuron ethyl/ha to 25 g/ha. BAS 1451
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be513f4b12dd108e51047c3ea6cb620a
https://doi.org/10.1515/znc-1991-9-1026
https://doi.org/10.1515/znc-1991-9-1026
Publikováno v:
Pesticide Biochemistry and Physiology. 41:66-81
[14C]Chlorimuron ethyl was readily absorbed by the roots of young intact corn seedlings and through the cut ends of excised leaves, but it was not readily absorbed by intact leaves. Under the conditions employed, [14C]chlorimuron ethyl was metabolize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90f3d695e0aef75647d13e03ffcb007f
https://doi.org/10.1016/0048-3575(91)90061-p
https://doi.org/10.1016/0048-3575(91)90061-p
Publikováno v:
Pesticide Biochemistry and Physiology. 39:291-301
[CF3-14C]Fluorodifen herbicide (2,4′-dinitro-4-trifluoromethyldiphenyl ether) was rapidly metabolized by a spruce cell suspension culture (Picea abies L. Karst). The primary route of metabolism involved cleavage of the diphenyl ether bond by glutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66761473588ba4dae58d4cfce822c136
https://doi.org/10.1016/0048-3575(91)90124-5
https://doi.org/10.1016/0048-3575(91)90124-5
Publikováno v:
Pesticide Biochemistry and Physiology. 37:211-218
Glutathione S-transferase activity was present in extracts from needles of two different spruce species (Picea abies and Picea glauca). In vitro conjugation studies were conducted with three 14C herbicides and one 14C fungicide: atrazine (2-chloro-4-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1f8f8a5e5f5edadbce4079962cb4142
https://doi.org/10.1016/0048-3575(90)90127-n
https://doi.org/10.1016/0048-3575(90)90127-n
Autor:
Gerald G. Still, Donald G. Rusness
Publikováno v:
Pesticide Biochemistry and Physiology. 7:232-241
Inhibition of S-cysteinyl-hydroxychlorpropham transferase from oat (Avena sativa L.) by various compounds was studied. The β-O-glucoside of the substrate, isopropyl-3′-chloro-4′-hydroxycarbanilate (4-hydroxychlorpropham), and isopropyl-3′-chlo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36a1d46ce69b7688ea8262524601771e
https://doi.org/10.1016/0048-3575(77)90014-1
https://doi.org/10.1016/0048-3575(77)90014-1
Autor:
Gerald G. Still, Donald G. Rusness
Publikováno v:
Pesticide Biochemistry and Physiology. 4:109-119
The firefly luciferase ATP assay was inhibited by the herbicide, isopropyl-3-chlorocarbanilate (I), and by two of its hydroxylated metabolites, isopropyl-5-chloro-2-hydroxycarbanilate (II) and isopropyl-3-chloro-4-hydroxycarbanilate (III). The β-O-g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a7029d84185b49aceaa80382b0f8ea2
https://doi.org/10.1016/0048-3575(74)90089-3
https://doi.org/10.1016/0048-3575(74)90089-3
Publikováno v:
Pesticide Biochemistry and Physiology. 23:108-115
The effects of CDAA ( N,N -diallyl-2-chloroacetamide) pretreatment on subsequent CDAA injury to corn were examined and compared with the effects of the herbicide protectant R-25788 ( N,N ,-diallyl-2,2-dichloroacetamide). In addition, the effects of C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d31d6850741fb78fd6420110c53cdda
https://doi.org/10.1016/0048-3575(85)90084-7
https://doi.org/10.1016/0048-3575(85)90084-7
Autor:
Gerald G. Still, Donald G. Rusness
Publikováno v:
Pesticide Biochemistry and Physiology. 4:24-30
The effects of the herbicide, isopropyl-3-chlorocarbanilate, and its hydroxylated metabolites, isopropyl-5-chloro-2-hydroxycarbanilate and isopropyl-3-chloro-4-hydroxycarbanilate, upon NADH oxidation, P i uptake or release, and ATP formation were stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8202fbe449be404c297ebebbc928408
https://doi.org/10.1016/0048-3575(74)90081-9
https://doi.org/10.1016/0048-3575(74)90081-9