The development of phloem transfer cells in expanded dark grown leaflets of pea seedlings (Pisum sativum) has been re‐examined. In agreement with previous observations transfer cells in leaflets maintained in the dark did not form wall ingrowths to the same extent as those placed in the light. A previous report that exposure to light in a carbon dioxide depleted atmosphere inhibited wall ingrowth formation could not be confirmed. It was found that dark grown leaflets could be induced to form wall ingrowths without illumination by immersing them in a glucose solution, demonstrating for the first time that light is not necessary for phloem transfer cell differentiation in leaves. Attempts were made to alter the carbohydrate level in the whole seedling by removing the cotyledons, but this had no recognizable effect on wall ingrowth formation in any of the treatments. Starch grain formation in the plastids was taken as an indication of available soluble carbohydrate level in the leaflets. It is concluded that both light and the presence of soluble carbohydrate can independently induce wall ingrowth formation in phloem transfer cells of pea leaflets.

The intracellular localization of acid phosphatases in stimulated digestive glands of Dionaea flytraps has been studied to provide evidence for the route taken by this enzyme during secretion. Previous studies have either included or excluded a role for the dictyosomes in this pathway. Both p-nitrophenyl phosphate and beta-glycerophosphate were used as substrates, and both gave similar localization patterns. Unstimulated glands contained little phosphatase activity in the endomembrane system, whereas 24 and 48 hr after stimulation, heavy deposits of lead were located in the endoplasmic reticulum cisternae, including the nuclear envelope, the dictyosome cisternae, and secretory vesicles. Since dictyosome activation, as judged by the presence of secretory vesicles in the cytoplasm, also coincides with gland stimulation, we conclude that secretion of the hydrolase enzymes occurs via this route and not, as suggested elsewhere, via direct endoplasmic reticulum to plasma membrane connections.

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