AXILLARY BUD DEVELOPMENT IN POPULUS DELTOIDES. I. ORIGIN AND EARLY ONTOGENY

1977 ◽  
Vol 64 (7) ◽  
pp. 835-848 ◽  
Author(s):  
Philip R. Larson ◽  
Thompson D. Pizzolato
1975 ◽  
Vol 5 (3) ◽  
pp. 367-380 ◽  
Author(s):  
M. G. R. Cannell ◽  
S. C. Willett

During 1973, bud formation was monitored by sampling terminal buds from the topmost branches on four provenances plus one interprovenance hybrid of 10-year-old Pinuscontorta, and five provenances of 8-year-old Piceasitchensis, all growing in forest trials in Scotland. On both species, extension growth occurred between late May and mid-July. On pine, buds began forming in April; about a third of next year's needles (axillary bud primordia) were formed before mid-July and all were formed by mid-September. On spruce, bud formation occurred from May to October.Northerly and inland montane provenances began producing primordia earlier in spring than southerly provenances, suggesting differences in temperature sensitivity. The dates when bud development ceased were more closely related to latitude of seed origin, suggesting differences in photoperiod sensitivity. Differences among pine provenances in total numbers of primordia formed were related to differences in maximum rates of initiation during the summer, whereas in spruce they were due to differences in seasonal duration. In all cases, rates of initiation were closely correlated with apical dome diameters. Implications are noted regarding conifer breeding and environment–genotype interactions.


2013 ◽  
Vol 8 (11) ◽  
pp. e27167 ◽  
Author(s):  
Masaki Niwa ◽  
Motomu Endo ◽  
Takashi Araki

HortScience ◽  
1996 ◽  
Vol 31 (5) ◽  
pp. 798-801 ◽  
Author(s):  
Unaroj Boonprakob ◽  
David H. Byrne ◽  
Dale M.J. Mueller

Actively growing shoots of peach [Prunus persica (L.) Batsch] were collected every 2 weeks throughout the 1989 growing season. The samples were sectioned longitudinally and transversely to observe axillary bud initiation, which occurred in all samples collected. Differentiation of axillary bud meristems from early season samples (mostly normal nodes) included apical and prophyll formation, with procambium connected to the stem procambium. Little to no differentiation of such structures occurred in the late-season samples (mostly blind nodes). Other results suggest that blind node formation is a consequence of a lack of bud differentiation rather than a failure of bud initiation.


1972 ◽  
Vol 50 (11) ◽  
pp. 2381-2387 ◽  
Author(s):  
Richard T. Riding

The pattern of branching in seedlings of Pinus radiata appeared to be correlated with the size and zonation of the shoot apex. Just before splitting of the seed coat, the apex reached a maximum size and granular storage products, present in the embryo, were no longer evident. Shortly after the seed coat split, the hypocotyl and cotyledons became green. The first needle primordia were formed alternate to the cotyledons. Zonation of the apex was evident at this time; however, the apical zone was homogeneous and cells of the pith–rib-meristem had not elongated. Buds were initiated in the axils of many of the first-formed needle primordia. Needle initiation progressed rapidly up the flanks of the apex, reducing it to a minimum size shortly after the cotyledons emerged from the seed coat. Nodes formed at this time had a low frequency of axillary bud formation. During early epicotyl elongation the rate of needle initiation decreased and cell divisions were evident throughout the apex. The apex then increased in size and developed a zonation similar to that found in mature plants. As the apex increased in size, the frequency of axillary bud initiation also increased.


1981 ◽  
Vol 59 (12) ◽  
pp. 2577-2591 ◽  
Author(s):  
Philip R. Larson ◽  
Jennifer H. Richards

The vasculature of elongating lateral branches of Populus deltoides Bartr. ex Marsh. was examined to determine how vascular continuity was attained around the entire branch circumference. In a previous study it was found that a pair of original bud traces (A, A′) gave rise to three pairs of bud traces in sequence (a, a′; b, b′; g, g′) that vascularized the axillary bud; the original bud traces then continued upward in the main stem axis. In this study we demonstrated that the lower, abaxial part of the branch cylinder was vascularized by derivatives of the first pair of bud traces (a, a′), the lateral parts primarily by derivatives of the second pair of bud traces (b, b′), and the upper, adaxial part by derivatives of the third pair of bud traces (g, g′). Thus, the organizational pattern for branch vascularization was established during the earliest stages of axillary-bud initiation. Leaves on all lateral branches were anisophyllous; the condition was related to the position of leaves in the phyllotactic array and to their vascularization. The smallest leaves always occurred on the upper branch side and their central traces were diverted upward in the main stem vascular cylinder. The largest leaves were usually on the lower stem side and their central traces were diverted downward. Some first-formed leaves were falcate, and the lateral traces serving the suppressed sides of their laminae were also found to be diverted upward in the main stem axis. It was suggested that both the small anisophyllous and the falcate leaves might result from a lower nutritional status because of their upward-directed leaf traces.


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