In 1997, 1-year-old, unbranched, ≈1-m-long shoots of the apple ( Malus × domestica Borkh.) rootstock `Merton-Immune 793' (MI.793) were selected at random from two commercial stoolbeds in the Western Cape, South Africa, during the dormant period. One site has mild winters [307 Utah Chill Units (CU) in 1997, 34°S, 300 m] while the other is moderately cold (1497 CU in 1997, 33°S, 950 m). In 1998, `Granny Smith' shoots were collected from a mature orchard in another warm area (574 CU in 1998, 34°S, 116 m). Shoots were prepared and forced at 25 °C with continuous illumination. During dormancy the developmental rate was determined of the terminal bud, and of both distally and proximally situated lateral buds, with or without the inhibitory influence of a distal disbudded shoot piece (10 cm long). In the moderately cold area, the growth rate of the terminal bud increased shortly before spring budburst such that a weak acrotonic tendency was established. The shorter dormant period, as experienced with the mild winters common to the apple-growing regions of the Western Cape, impeded the full development of acrotony and subsequent apical control. With less chilling (mild areas) a basitonic tendency remained. Budburst was slower and more erratic, and inhibition by the distal shoot parts was accentuated. Delayed foliation may be due more to correlative inhibition than to endodormancy. When lateral buds are released from paradormancy they exhibit a growth potential similar to, or, with less chilling, even greater than, that of the terminal bud. This permits a greater expression of autonomy between shoots.
Two-year-old apple branches, ≈50 cm long, were selected from a commercial `Royal Gala' orchard in the Ceres (Koue Bokkeveld) region of the Western Cape, South Africa [33 °S, 945 m, 1500 Utah model chilling units (CU)]. In 2000, the branches received either cold storage at 5 to 7 °C or natural chilling in the field. In 2001, the trial was repeated, but only with field chilling. The branches received five dormant pruning treatments: control (not pruned); pruning back to the fourth lateral shoot (heading) before or after chilling; and removal of the second and third lateral shoots (thinning) before or after chilling. After pruning and chilling, the branches were removed from the orchard or cold room every 2 weeks and forced in a growth chamber at 25 °C. The rate of budburst (1/days to budburst) was determined for the terminal buds of the lateral shoots. Lateral shoots on the 2-year-old branches were categorized according to position: the most distal extension shoot, and all other laterals grouped. Removing distal tissue by pruning (heading more than thinning) enhanced the effect of chilling on the terminal buds on the lateral shoots and promoted budburst. Pruning was more effective before than after chilling. Pruning enhanced the growth potential of the terminal buds on proximal shoots on 2-year-old branches.
One-year-old shoots of apple ( Malus ×domestica Borkh.) rootstock Malling 9 (M.9 clone Nic 29), ≈60 cm long without sylleptic side shoots, were selected randomly from a commercial stoolbed in Belgium, prepared, and forced at 25 °C and 16 hours daylength to follow bud developmental rate in different positions along a 1-year-old shoot. The number of buds that reached green tip was recorded daily until 50% of shoots exhibited budburst. The evolution of dormancy of the terminal, an upper lateral, and a lower lateral bud was followed throughout the dormant period. The influence of a distal disbudded shoot piece and Promalin [3000 mg·L -1 N -(phenylmethyl)-1 H -purine 6-amine and 3000 mg·L -1 gibberellins A 4 +A 7 without a wetting agent] application on the developmental rate of these buds was evaluated. Bud developmental rate decreased during winter and increased to a maximum before budburst in spring. The distal shoot-forming ability or acrotonic branching habit in apple appears to be mediated via a greatly increased developmental rate of the terminal bud relative to the upper and lower lateral buds, respectively. The proximal budbursting tendency or basitony exhibited in early winter was weak compared to the acrotony that developed in the last month before budburst in spring. Lateral buds showed a lower developmental rate than the terminals when inhibited by a distal disbudded shoot piece, so that resultant overall growth habit within the shoot remained acrotonic throughout the dormant period. Promalin application in winter did not restore the bud developmental rate associated with spring budburst. These results are discussed with reference to observations of trees growing under conditions of insufficient winter chilling.