Investigations were conducted to elucidate the mechanism of selectivit
y of the auxin herbicide, quinmerac, in cleavers (Galium aparine) and
the tolerant crops sugarbeet (Beta vulgaris), oilseed rape (Brassica n
apus) and wheat (Triticum aestivum). After root treatment with the her
bicide, the selectivity has been quantified as approximately 400-fold
between oilseed rape and Galium and 1000-fold between sugarbeet or whe
at and the weed species. When 1 and 10 mu M [C-14]quinmerac were appli
ed for 4 h, no significant differences between root absorption and tra
nslocation of C-14 by Galium and the crop species were found. After 16
h, metabolism of [C-14]quinmerac to the biologically inactive hydroxy
methyl and dicarboxylic acid derivatives was more rapid in wheat and s
ugarbeet than in Galium. In oilseed rape, a lower rate of herbicide me
tabolism was observed. In Galium, accumulations of abscisic acid (ABA)
, triggered by quinmerac-stimulated ethylene biosynthesis, were found
to cause the herbicidal growth inhibition which develops during 24 h o
f application. Within 1 h of treatment, quinmerac stimulated 1-aminocy
clopropane-1-carboxylic acid (ACC) synthase activity and ACC concentra
tion specifically in Galium shoot tissue. During the next 4 h, ACC syn
thase activity was increased up to 50-fold, relative to the control. W
ithin 3 h of exposure to quinmerac, increased ethylene formation follo
wed by higher ABA levels was detected. In sugarbeet, oilseed rape and
wheat, quinmerac did not stimulate ACC synthase activity and ACC and A
BA levels. It is suggested that (i) the selectivity of quinmerac is pr
imarily based upon the lower sensitivity to the herbicide of the tissu
e/target in the crop species, (ii) the induction process of the ACC sy
nthase activity in the shoot tissue is the primary target of herbicida
l interference. In wheat and sugarbeet, tolerance to quinmerac is addi
tionally increased by a more rapid metabolism (C) 1998 SCI.