The role of light in the isomerization and cyclodimerization of the ci
nnamic acid component of plant cell walls has been examined in a numbe
r of ways. Cinnamic acid derivatives were extracted from neutral deter
gent fibre cell walls by alkaline hydrolysis and quantified by GC. Amo
unts of these acids in leaf and stem tissues of barley straw which had
naturally been exposed to very different levels of radiation were com
pared. Leaf cell walls contained less p-coumaric acid than stem cell w
alls, but a higher proportion of this was found as the (Z)-isomer and
cyclodimer (4,4'-dihydroxy-alpha-truxillic acid). Samples of wheat str
aw from a sequence of 10 consecutive years, grown under conditions whe
re meteorological conditions were the major variable, showed considera
ble year-to-year differences; the (Z)-/(E)-ratio and dimer/monomer rat
io varied three-fold. Additional studies compared the direct effect of
light on the cinnamic acid derivatives in growing barley seedlings (l
ive), freeze-dried seedlings (dead) and freshly harvested straw sample
s (dead). There were no significant changes in the cinnamic acid deriv
atives extracted from the cell walls of dead tissue which had been sto
red in the dark. Storage in light resulted in increased (Z)-isomer and
cyclodimer contents. These changes occurred whether the tissue was al
ive or dead. They can, therefore, be directly attributed to the effect
of light, and do not appear to be mediated by any enzymic reactions.