Influence of Season, Population, and Spacing on Axillary Bud Development of Sweet Corn 1

1967 ◽  
Vol 59 (4) ◽  
pp. 355-358 ◽  
Author(s):  
R. H. Andrew
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.


1996 ◽  
Vol 121 (3) ◽  
pp. 543-547 ◽  
Author(s):  
Mark A. Ritenour ◽  
Ellen G. Sutter ◽  
David M. Williams ◽  
Mikal E. Saltveit

This study was undertaken to determine if endogenous IAA content and axillary bud development correlate with phenylalanine ammonia-lyase (PAL) induction and russet spotting (RS) susceptibility among RS susceptible and resistant cultivars of Iceberg lettuce (Lactuca sativa L.). Final levels of ethylene-induced PAL activity and RS development were highly correlated among cultivars, field conditions, and harvest dates. Harvested Iceberg lettuce midribs contained relatively low amounts of free IAA (maximum of 5.2 ng·g-1 fresh weight). There was poor correlation between free IAA content in lettuce leaf midribs and final RS development among all cultivars, growing conditions, and harvest dates. Axillary bud development, as measured by the number of visible buds per head, bud weight, or bud length, were not significantly correlated with final RS development or midrib IAA content. Cultivars with higher initial free IAA content lost much of their IAA after 8 days storage at 5C in air ± ethylene.


HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 544d-544
Author(s):  
James E. Faust ◽  
Royal D. Heins

Poor lateral branching sometimes occurs when certain poinsettia (Euphorbia pulcherrima) cultivars are pinched. Two experiments were conducted to determine the effect of high temperatures on axillary bud development. In Expt. 1, `Red Sails' plants were grown in a high-temperature environment (HTE) of 27°C at night (8 hr) and 30°C (3 hr), 33°C (10 hr), and 30°C (3 hr) in the day for two months, then transferred to a 20°C environment. In Expt. 2, plants grown at 20°C were transferred into the same HTE described above for 0, 2, 4, 8, 16, or 32 days and were then moved back into the 20°C environment. Axillary buds were examined for viability at the end of each experiment. In Expt. 1, only 8% of the lateral buds forming in the HTE were viable, while 80% of the buds forming in leaf axils of leaves unfolding after the plants were transferred to the 20°C environment were viable. In Expt. 2, 80% of buds produced in axils of the first four leaves to unfold after the start of the experiment were viable in all the treatments. However, the percentage of viable buds in the axils of leaf numbers 5 to 8 was 100, 100, 100, 96, 56, and 0 for the plants placed in the HTE for 0, 2, 4, 8, 16, and 32 days, respectively. These data indicate day temperatures of 30 to 33°C adversely affect lateral shoot development of `Red Sails' poinsettia.


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