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‘Royal Gala’ apple scions (Malus ×domestica) were grafted onto 1-year-old rootstock stools of ‘M.9’ (M.9), ‘M.M.106’ (MM.106), ‘Merton 793’ (M.793), and ‘Royal Gala’ [R.G (control)] to elucidate how the dwarfing apple rootstock (M.9) modified scion architecture, the time from grafting when this started, and whether changes in scion architecture were explained by some endogenous hormones present within the scion. At the end of the first season of growth (April), the final length and node number of the primary shoot were similar for scions on M.9 and R.G. However, M.9 appeared to limit the number of secondary shoots formed on the primary shoot during summer. In addition, the proportion of secondary shoots that were actively extending in fall was lower for M.9; consequently, the final mean length of the secondary shoots was slightly shorter for M.9 compared with R.G. Collectively, these subtle effects of M.9 significantly reduced the final total shoot length of the scion compared with R.G. The final dry weight of the scion and root system was also lower for M.9 than MM.106, M.793, and R.G. The mean rate of indole-3-acetic acid diffusing from the apex of the primary shoot progressively declined from February onward irrespective of rootstock, whereas the mean concentration of zeatin riboside (ZR) in the xylem sap increased during the same period, and these events appeared to coincide with cumulative increases in the number of axillary growing points formed on the scion. Despite this general trend, M.9 had a greater concentration of ZR in the xylem sap during February compared with R.G, but the primary shoot on M.9 did not develop more axillary growing points, indicating that other endogenous hormonal signals were also involved in regulating scion branching. By March, M.9 lowered gibberellin A19 (GA₁₉) concentration in the xylem sap of the scion significantly compared with R.G. We conclude that dwarfing apple rootstocks may limit root-produced GA₁₉ supplied to shoot apices of the scion, where GA₁₉ may be a precursor of bioactive gibberellin A1 required for shoot extension growth.

The time to harvest maturity of flowering shoots and the extent and source of variability in maturity dates differed among cultivars of gentian (Gentiana sp.), with a wider spread in time to harvest maturity in Showtime Starlet (41 days) than Showtime Diva (35 days) and Showtime Spotlight (29 days). Cultivars also differed by more than twice in their plant-to-plant variability in time to harvest. Although later-emerging shoots reached harvest maturity more quickly than earlier-emerging shoots, the use of growing degree-days (GDD) for this field-grown cut flower did not account for differences. For ‘Showtime Diva’, 77% of outliers reached harvest maturity at the beginning of the season (i.e., before the 10th percentile). For ‘Showtime Spotlight’, only 20% of shoots classified as outliers flowered early with the remaining 80% emerging late (i.e., after the 90th percentile). Strategies to control the spread in time to harvest maturity in late-maturing cultivars such as Showtime Starlet should focus on uniform shoot emergence and controlling temperature during growth. Although strategies to achieve uniform shoot emergence should also be targeted for ‘Showtime Diva’, controlling temperature during the growing season would not appear to offer significant control of the spread in time of harvesting floral shoots. However, in earlier-maturing cultivars such as Showtime Spotlight, strategies will primarily require a greater understanding of the factors influencing the variability in maturation of shoots within individual plants before, and after, emergence.

Cut flower productivity and quality of gentian is associated with growth and development of crown buds. Experiments were carried out with the gentian cultivar Showtime Diva to identify the response to treatments that break dormancy [cold temperature (chilling), gibberellic acid (GA₃)] applied at different stages of development of crown buds (plants with nonemerged crown buds, shoots recently emerged, or shoots emerged and elongated). The comparative growth potential of crown buds within the cluster was also investigated. At the stages of development examined, the application of GA₃ (100 ppm) increased emergence of crown buds as shoots, leading to development of more flowering shoots. A similar response was observed with exposure to cold, but only on plants with nonemerged crown buds. Shoot emergence increased in response to increased duration of cold from 0 to 42 days (5 °C). Both chilling and GA₃ could potentially be used to reduce the duration to, and spread of, harvest maturity if applied before shoot emergence. The hierarchical relationship of buds in crown bud clusters led to differential responses to application of GA₃. Buds ontogenetically positioned at the proximal end of the bud cluster took a similar duration to reach shoot emergence or harvest maturity. For buds located at the distal end there was a positive correlation between ontogenetic bud position and the duration to reach shoot maturity. Shoot length and number of nodes at harvest maturity showed slight negative correlations with the position of the bud in the bud cluster. The results provide an explanation for possible sources of the variation in quality and quantity of floral shoots, and spread in time to harvest maturity within a single plant, and with development stage.

We investigated the possibility of either exogenous ethylene or endogenous ethylene production having an association with the increase in shoot number when nodal explants of Gentiana spp. ‘Little Pinkie’ were cultured in an in vitro medium supplemented with ethephon (10 mg⋅L^–1). For the first time within an in vitro system, we report the application of laser ethylene detector technology, and optimization of the methodology to quantify concentrations of ethylene (in the part-per-billion range) released from ethephon decomposition within the atmosphere of gas-exchangeable culture vessels including nodal explants. Compared with continuous (continuous measurements on the same replicate of vessels) and repeated (sampling same replicate of vessels every 48 hours) sampling methodologies, the nonrepeated (sampling fresh replicate of vessels every 48 hours) method of measurement of ethylene concentration was more representative of the actual condition within vessels. Although no prior published data exist showing the positive or negative effect of gaseous ethylene in the headspace of culture vessels on bud outgrowth in gentian, our study shows gaseous ethylene in the headspace of culture vessels was not effective in increasing shoot formation in gentian explants cultured in vitro, whereas ethephon supplementation in agar was effective. Plant material in culture vessels did not have a significant effect on ethylene production regardless of the presence or absence of ethephon. Therefore, although ethephon supplementation in the medium produced gaseous ethylene in the headspace, it was unlikely to cause endogenous ethylene production in explants, but it did trigger shoot formation in ‘Little Pinkie’, perhaps through decomposition to ethylene within the explant tissue, enhancing the internal ethylene level possibly at a locally high concentration.

Shoot productivity and overwintering survival of gentians (Gentiana sp.) are determined by the initiation and subsequent development of crown bud clusters. Understanding of the anatomical features and origins of crown buds and bud clusters, and plant ontogeny, the morphological features of crown buds, and their associated development is required to achieve manipulation of bud initiation, emergence, and development. Anatomical features of the crown bud clusters were examined using both light and confocal microscopy using hybrids of Gentiana triflora × G. scabra. The initiation of bud clusters presented characteristics typical of adventitious buds in terms of their origin and presence of external vascular connection to the parental tissue. In contrast, crown buds forming subsequently within the cluster developed as axillary buds within that initial bud, collectively forming on a compact stem with minimal internode elongation. Stem elongation within the cluster after application of gibberellic acid enabled identification of a hierarchical arrangement of buds within the cluster with one bud at each node and arranged spirally at 90°. Arrangements of buds within the cluster were different from the opposite decussate phyllotaxis in floral shoots with two axillary buds at each node. Based on the current study, a crown bud cluster originated from a first bud initial, which was adventitious followed by development of subsequent crown buds within the cluster as axillary buds from this first bud initially with a single bud developing at each node.