MATERIALS AND METHODSPhotochemical development was studied in developing cucumber (Cucumis sativus L. cv Hokushin) leaves to determine if the spatial pattern coincided with relative growth rates of expanding leaves, intercalary cell division, or position relative to the vascular tissue. Both leaf surfaces undergo a series of similar changes in chlorophyll a fluorescence kinetics, but the upper surface more quickly achieved the characteristic response. Imaging of fluorescence showed an individual developing leaf has four regions differing in kinetics, but these regions do not coincide with areas of increasing relative growth rate. Two of these regions lie at the leaf edge and their divergent kinetics may be related to structural and physiological features present at this position. A third area with different kinetics, in the basal region of the leaf, is spatially consistent with primordial regions that are clonal during development. The correspondence between areas of clonal growth and specific fluorescence kinetics indicates that cells of common ancestry show functional uniformity. No evidence was found that the proximity of the vascular tissue influenced development of photochemical function.The attainment of photosynthetic competency in angiosperm leaves is regulated by light and by developmental factors. Unlike monocots such as wheat (2), cucumber leaves are not photochemically competent when first exposed to light, but acquire competency over an extended time period, 6 d or more in the light (5). Within these leaves photochemical activity is not homogeneous, but develops basipetally as shown by Chl a fluorescence transients. These data indicate that the primary regulation ofthe development ofphotochemical activity lies with developmental factors, not light (5).Although the attainment of characteristic fluorescence transients progresses in a basipetal direction, mirroring the general direction ofexpansion and growth ofthe leaf(5), the influence of developmental factors from cells and tissues within the leaves has not been studied. The objective of the present research was to determine ifthe spatial pattern of photochemical development coincided with leaf expansion and relative growth rates, intercalary cell division, or position relative to the vascular tissue. With the availability of dynamic imaging of Chl a fluorescence (10), a precise, nondestructive means of studying these influences exists.'Supported by a National Science Foundation grant (JGC).
Plant Materials and Leaf Area MeasurementsCucumber (Cucumis sativus L. cv Hokushin) plants were grown as previously described (10) for up to 5 weeks. For fluorescence and gas exchange measurements, plants were brought from the controlled-environment greenhouse to the laboratory and allowed to acclimate for about 2 h. Plants were dark-incubated for at least 30 min before fluorescence induction. No appreciable differences in induction kinetics were observed with longer dark periods. Leaves monitored for fluorescence and assimilation were intact and remain...