HORMONAL CONTROL OF ORGANOGENESIS IN OPUNTIA POLYACANTHA (CACTACEAE)

Abstract

An axillary bud (areole) of Opuntia polyacantha is composed of an extremely short axis which bears highly modified leaves (spines). After producing the spines, the bud apical meristem becomes quiescent. When the axillary bud is excised and cultured with benzylaminopurine (BAP), the apical meristem increases in complexity and produces leaves on an elongated axis. Gibberellic acid (GA) induces spine production with no elongation of the axis. Naphthaleneacetic acid (NAA) causes no structural change in the meristem but induces root formation in adjacent tissue. The initiation of roots, spines, or leaves is visible within three days. Explants on medium lacking hormones show no structural change, but by the tenth day are insensitive to BAP or NAA. These aged explants can be made to respond to BAP or NAA by merely rewounding them at the time of hormone application. With concentrations previously found to be optimal for single hormone responses, NAA in combination with BAP prevents shoot formation, or in combination with GA prevents spine production. When all three hormones are combined, spines are produced, indicating that GA is active morphologically while BAP and NAA counteract each other. If the level of NAA is decreased, BAP counteracts the NAA and also overrides the GA and leafy shoots are produced. By varying the proportions of BAP and GA, in the absence of NAA, four types of lateral appendage can be produced: leaves, mildly altered leaves, leaf‐spine transition forms, and spines.