Oat (Avena sativaL. ‘Elgin′) and soybean (Glycine maxL. ‘Evans′) were treated with14C-diclofop-methyl {methyl ester of 2-[4-(2,4-dichlorophenoxy)phenoxy] propionic acid]} or14C-diclofop alone or in combination with 2,4-D [(2,4-dichlorophenoxy)acetic acid] or bentazon [3-isopropyl-1H-2,1,3-benzothiadiazin-4(3H)-one 2,2-dioxide] and14C-2,4-D alone or in combination with diclofop-methyl or diclofop. More radioactivity was recovered in the treatment zone after14C-diclofop-methyl applications, alone or in combination, than after similar14C-diclofop treatments in oat and soybean. Basipetal movement of radioactivity was 4 and 1% and acropetal movement was 1 and 4% in oat and soybean, respectively, regardless of the diphenyl ether treatment or time. Addition of 2,4-D or bentazon did not reduce translocation of radioactivity from14C-diclofop-methyl treatments in either plant species. Basipetal movement of radioactivity from14C-diclofop-methyl was greater than from14C-diclofop in both oat and soybean. The addition of diclofop-methyl or diclofop did not affect the pattern or amount of14C-2,4-D radioactivity translocated. In oats, radioactivity appeared to accumulate within the intercalary meristematic region with14C-2,4-D and14C-diphenyl-ether applications. Diclofop-methyl at 1 kg/ha applied either to an entire oat plant at the three-leaf stage or the apical meristemic region resulted in plant mortality. The extent to which transport contributes to diclofop-methyl efficacy is questioned.
Leukodystrophy caused by plasmalogen deficiency rescued by glyceryl 1‐myristyl ether treatment
