Pistillate flower development and acorn production were observed in small populations of white oak (Quercus alba L.) and black oak (Quercus velutina Lam.) in central Missouri from 1990 to 1997. There were significant year-year differences in the size of flower crops for both species and significant tree-tree differences in black oak. About 7% of the white oak flowers matured into acorns; most flowers aborted by early July, just after fertilization. About 12% of the black oak flowers matured into acorns, but some individual trees never or rarely produced a mature acorn. The number of fertilized flowers in white oak and black oak in early July was positively correlated with acorn production. Over all trees and years, the number of flowers and acorns were significantly correlated. Acorn production varied in relation to weather variables during the time of pollination. Simple regression models were good predictors of white oak acorn production but not of black oak acorn production. Maximum temperature and the number of days with hail had negative effects on acorn production. The number of days of rain during the pollination period was positively correlated with flower survival in black oak but not with white oak.
Precocious flowering provides opportunities to shorten a breeding cycle. A tree may flower for the first time when sufficient crown development has occurred and there are enough meristems to support both vegetative and reproductive buds. Precocious flowering can be promoted through the use of cultural techniques, such as photoperiod, accelerated growth, gibberellins and water stress. The length of the juvenile phase is dependent on genetic and environmental variables that affect achievement of a minimum size, and is positively correlated with the height of the plants within a family. Selection pressure can be applied successfully to the precocious flowering character, and crossed or inbred lines of precocious flowering progeny can be developed. Various levels and amounts of genetic control have been implicated in the control of precocious flowering.
Seedlings of three families of jack pine (Pinus banksiana Lamb.) were subjected to 16 combinations of photoperiod, growth environment (outdoors, greenhouse and biotron) and gibberellin (GA(4/7)) treatment. After 14 months, which included two dormancy induction periods, ovulate flowering was observed. There was a strong positive correlation between flowering and seedling height; female flower production was stimulated by both a declining photoperiod during bud development and GA(4/7) treatment; and there was an interaction between GA(4/7) treatment and family, such that the difference in flowering intensity between a late-flowering and an early-flowering family was eliminated by GA(4/7) treatment. The results suggest that the genetic control over the time of onset of flowering, and GA(4/7)-induction of flowering depend on a common mechanism.
The morphology and anatomy of the shoot apex in germinating Pinus banksiana seeds is described by using scanning and transmission electron microscopy and microspectrophotometry, with special attention given to events preceding the appearance of the first leaf primordia at about 72 hr post‐imbibition. The 2C nuclei begin DNA synthesis at about 43 hr. RNA increases until 52 hr and is followed by a reduction related to cytokinesis. Protein drops after 36 hr, apparently related to digestion of storage protein bodies, which by 48 hr are about 50% digested. The resulting protein body vacuoles do not enlarge. Starch is digested just prior to appearance of the leaves and may be mediated by α‐amylase production from stacks of endoplasmic reticulum. Heterochromatin increases in the nuclei during germination and coincides with an increase in repeated nucleotide sequences. Golgi bodies increase in number after the first mitoses.
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