With the inflorescence removed, intercalary growth can be maintained in the scape of Gerbera jamesonii by application of gibberellic acid (GA, gibberellin A 3 ) or indole‐3‐acetic acid (IAA); the latter usually promotes more rapid and greater elongation than the former because of a greater effect on older tissues. Simultaneous application of the two substances, even when both are at optimal levels, promotes more rapid elongation than either substance alone; in fact, the rate of elongation may equal that of the intact scape. In decapitated scapes (receptacle and involucral bracts removed with the inflorescence), GA and IAA promote cell elongation with reduced or no cell division. In deflowered scapes (receptacle and involucral bracts intact) both GA and IAA promote cell division, as well as cell elongation, so that the pattern of scape elongation is nearly the same as that for intact scapes. Apparently the bracts and receptacle contribute something required for cell division which acts in concert with GA and IAA. Deflowered and decapitated scapes elongate at nearly the same rates initially; thus the rate of elongation does not depend on cell division. The ultimate length of the scape is dependent on cell number and, hence, cell division, since deflowered scapes attain greater lengths than those that are decapitated.
No takes yet. Share an insight, caveat, or question.
Roy M. Sachs (1968) studied this question.
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: