Thiamine-"C moved through petiolar sections of Lycopersicon esculentum Mill. var. Michigan State Forcing with striking similarity in kinetics to auxins and gibberellic acid moving through similar sections of other green plants. Thiamine moved with strong basipetal polarity, at a velocity of 3 to 5 mm per hour, and emerged unchanged into the basal receiver agar block, judging by chromatography. This lends support to the hypothesis that polar movement is a property of several classes of plant hormones, rather than being restricted to the auxins (as previously believed).Multicellular plants show many polar phenomena during development and regeneration (e.g., regeneration of roots at the basal or "root" end of an excised stem section). Some of these phenomena have been explained as being manifestations of the movement of the plant hormones known as auxins, which have been known to move polarly since 1928 (10,19). After it was shown (7,8,11,16) that even the synthetic auxin-type herbicide 2, 4-D moved through excised shoot tissues with a polarity like that of the endogenous auxin IAA, other classes of hormones were tested. Just recently, GA. was found to move with a polarity very similar to IAA through Coleus petioles and with opposite polarity to IAA through corn root sections (12)(13)(14). Although early reports claimed polar movement of abscisic acid and a cytokinin (1, 4), the more quantitative later studies found sizeable movement in both directions, with no clear sign of polarity of these two classes of hormone (5,9,18 considered as confirmation of the hypothesis that in the intact plant thiamine was synthesized in the leaves and moved from there to the roots, which were unable to synthesize it but needed it for development. We could find no literature on the movement of thiamine through classical "transport sections." So that the results would be more useful for comparisons, we used the same general methods used earlier in this laboratory for studies of the movement of auxins, cytokinins, and GA3 (10-14, 16, 18). Sections 5.1 mm long were excised with a double-bladed cutter from the middle of petioles of leaves of tomato (Lycopersicon esculentum Mill. var. Michigan State Forcing). Tomato was used because of the numerous reports that its excised roots need thiamine for continued growth in culture. The excised petiolar sections were placed horizontally between donor and receiver blocks of 1.5% agar (see inset diagram of Fig. 1). Donor blocks contained thiamine, with stated specific radioactivity of 18.9 mc/mmole labeled with "4C in the thiazole 2 position, at a concentration of 15 uM. A donor block was placed against the apical ("leaf blade") end of the petiolar section when movement in the basipetal direction was being tested (as in inset diagram), and against the basal cut end (stem end) when acropetal movement was being tested. These transport systems were placed on glass slides in moist Petri dishes which were placed in a dark incubator at 26 to 27 C. After 2, 3, or 4 hr the receiver blocks were remo...