Bud development in Larix occidentalis. I. Growth and development of vegetative long shoot and vegetative short shoot buds

1979 ◽  
Vol 57 (7) ◽  
pp. 687-700 ◽  
Author(s):  
John N. Owens ◽  
Marje Molder
Keyword(s):  
Growth And Development ◽  
Shoot Elongation ◽  
Growth Cycle ◽  
Leaf Primordia ◽  
Axillary Buds ◽  
Larix Occidentalis ◽  
Short Shoot ◽  
Bud Development ◽  
Shoot Buds ◽  
Vegetative Bud

Vegetative terminal long shoot buds (TLSB) and short shoot buds (SSB) were studied throughout the annual growth cycle in several trees over several years. TLSB were not totally preformed. The dormant TLSB consisted of bud scales enclosing some basal leaves and both were borne on a broad receptacle. Centripetal to the basal leaves, a series of axial leaf primordia was borne on the flanks of the apex. After dormancy a second series of axial leaves was initiated above those initiated before dormancy. Basal and both series of axial leaves elongated during shoot elongation as the terminal apex again initiated axial leaves, bud scales, and then basal leaves. After shoot elongation the first series of axial leaves was initiated before the TLSB became dormant in October. No dimorphism occurred between predormancy and postdormancy axial leaves or axial and basal leaves. Axilliary buds were initiated in the TLSB about the time of flushing. All leaves did not bear axillary buds. All axillary buds rapidly initiated a series of bud scales and then entered a slower phase of bud-scale initiation and rapid apical enlargement. Leaf primordia then were initiated at the base of the apex and borne on the broad receptacle. Apices then differentiated into axillary long shoot buds (ALSB) or SSB. ALSB developed similarly to TLSB, whereas axillary SSB initiated leaf primordia at the base of the apex and all but the last primordia to be initiated were borne on the broad receptacle. Axillary SSB were preformed but ALSB were not completely preformed and both became dormant in mid-October. The apex of a short shoot lived for up to 8 to 10 years. In each successive year it passed through phases of bud-scale initiation and leaf initiation to form a dormant preformed SSB which flushed after overwintering. Annual short shoot elongation was about 1 mm. The LSB and SSB apices varied in shape and size during the year but apical zonation was similar in all apices. Larix vegetative bud development is compared with that found in other gymnosperms.

Bud development in Picea engelmannii. I. Vegetative bud development, differentiation, and early development of reproductive buds

1983 ◽  
Vol 61 (9) ◽  
pp. 2291-2301 ◽  
Author(s):  
Derek L. S. Harrison ◽  
John N. Owens
Keyword(s):  
Shoot Elongation ◽  
Longitudinal Axis ◽  
Leaf Primordia ◽  
Axillary Buds ◽  
Picea Engelmannii ◽  
Bud Burst ◽  
Bud Development ◽  
Vegetative Buds ◽  
Terminal Buds ◽  
Mother Cells

Vegetative buds of Engelmann spruce (Picea engelmannii Parry) from the Prince George Forest District (British Columbia) were collected and studied. In mid-April, dormancy ended as determined from mitotic divisions within the leaf primordia; 2 weeks later mitotic activity occurred in the bud apices. Bud-scale initiation began in terminal buds by late May followed by that in axillary buds 2 weeks later. Shoot elongation began in late May, bud burst occurred in late June, and both shoot elongation and bud-scale initiation were complete by late July. Terminal buds began to differentiate by the initiation of leaf primordia, into vegetative buds early in August whereas axillary buds began to differentiate 1 week later. Leaf initiation was completed in all vegetative buds by late September and buds were dormant by mid-October. Pollen cones initiated microsporophylls after bud-scale initiation. Microsporangial initiation began in late August. Microsporangial enlargement began in mid-September and continued until dormancy when pollen mother cells were observed in a premeiotic stage. Seed cones initiated bracts directly after bud-scale initiation. In mid-August, ovuliferous scales began to be initiated. Two ovule primordia formed adaxially, one on each side of the median longitudinal axis of each ovuliferous scale. Each ovule formed one large central megaspore mother cell which overwintered in a premeiotic stage.

Bud development in western hemlock. I. Annual growth cycle of vegetative buds

1973 ◽  
Vol 51 (11) ◽  
pp. 2223-2231 ◽  
Author(s):  
John N. Owens ◽  
Marje Molder
Keyword(s):  
Mitotic Activity ◽  
Shoot Elongation ◽  
Growth Cycle ◽  
Leaf Primordia ◽  
Annual Growth ◽  
Western Hemlock ◽  
Bud Burst ◽  
Bud Development ◽  
Vegetative Buds ◽  
Number Of Leaves

Vegetative apices of mature Tsnga heterophylla (Raf.) Sarg. were studied throughout the annual growth cycle. Apices become mitotically active during the last week of March. Leaf primordia elongate, causing the buds to swell, while the apex remains small and produces bud scales. Axillary buds are initiated about mid-April. Little shoot elongation occurs before vegetative buds burst in mid-May. After bud burst, rapid shoot elongation occurs for about 7 weeks, during which time the apex also elongates and the rest of the bud scales are initiated. There is a marked increase in mitotic activity in the apex during the transition from bud-scale initiation to leaf initiation, which occurs early in July when the grand phase of shoot elongation is complete. This is believed to be the time when vegetative apices undergo transition to become reproductive apices. Leaf primordia are initiated in rapid succession until mid-August, when two-thirds of the final number of leaves are initiated and the subtending shoot is fully elongated. From mid-August until mid-November, no shoot elongation occurs, leaf primordia are initiated more slowly, and mitotic activity in the apex gradually decreases. After all of the next season's leaves have been initiated, about mid-November, mitotic activity in the apex stops and the vegetative buds become dormant.

Bud development in Sitka spruce. I. Annual growth cycle of vegetative buds and shoots

1976 ◽  
Vol 54 (3-4) ◽  
pp. 313-325 ◽  
Author(s):  
John N. Owens ◽  
Marje Molder
Keyword(s):  
Early Period ◽  
Shoot Elongation ◽  
Growth Cycle ◽  
Picea Sitchensis ◽  
Leaf Primordia ◽  
Annual Growth ◽  
Bud Burst ◽  
Leaf Initiation ◽  
Number Of Leaves ◽  
Vegetative Bud

Vegetative apices of Picea sitchensis (Bong.) Carr. were studied throughout the annual growth cycle. Apices became mitotically active late in March and the shoot axis and leaf primordia elongated causing the bud to swell. New axillary apices were initiated in mid-April and the terminal apex and new axillary apices initiated bud scales until early in July. Vegetative bud burst occurred early in June and shoot elongation was completed by mid-July. The end of shoot elongation coincided with the onset of leaf initiation. The change from bud-scale to leaf initiation was characterized by a period of increased mitotic activity and rapid apical growth. About half of the final number of leaves were initiated during the early period of rapid leaf initiation. The remaining leaf primordia were initiated more slowly over the next 3 months. Buds became dormant by mid-November.

Bud development in Picea glauca. I. Annual growth cycle of vegetative buds and shoot elongation as they relate to date and temperature sums

1977 ◽  
Vol 55 (21) ◽  
pp. 2728-2745 ◽  
Author(s):  
John N. Owens ◽  
Marje Molder ◽  
Hilary Langer
Keyword(s):  
Picea Glauca ◽  
Shoot Growth ◽  
Shoot Elongation ◽  
Growth Cycle ◽  
Bud Dormancy ◽  
Annual Growth ◽  
Bud Development ◽  
Leaf Initiation ◽  
Vegetative Buds ◽  
Vegetative Bud

Vegetative buds of Picea glauca (Moench) Voss were studied throughout the annual growth cycle in several trees in 1975 and 1976 and bud development was related to lateral vegetative shoot growth, date, and temperature sums.Vegetative buds became mitotically active in mid-April at lower elevations and about 6 weeks later at higher elevations. Shoot elongation was characterized by similar smooth sigmoid curves in both years. Shoot growth was slow for the 1st month, rapid during the 2nd month, and slow again for the 3rd month and ended by early August. Temperature sums related best to percentage of shoot elongation if the end of vegetative bud dormancy was used as the starting date and 5 °C was used as the threshold temperature. Arbitrarily chosen starting dates and threshold temperatures gave temperature sums which were related to shoot elongation only when shoot elongation was nearly completed. Generally, if the end of vegetative bud dormancy is known, the number of days from that time is nearly as accurate as the more complex use of temperature sums in predicting the percentage of shoot elongation or the stage of vegetative bud development.Bud-scale initiation occurred during shoot elongation. Axillary buds were initiated in mid-May and flushing occurred when shoots had elongated to about 30% of their final length in late May or early June. The end of shoot elongation coincided with the onset of leaf initiation on all trees in both years. The change from bud-scale initiation to leaf initiation was preceded by a marked increase in apical width and a slight increase in apical height and mitotic frequency. Leaf initiation was rapid for 6 weeks then slower for the last 4 weeks. Vegetative buds became dormant in mid-October.Vegetative bud development is closely related to shoot elongation. Breaking of vegetative bud dormancy was not affected by temperature but shoot elongation and flushing were affected by temperatures which occurred after dormancy was broken.

Bud development in Larix occidentalis. II. Cone differentiation and early development

1979 ◽  
Vol 57 (14) ◽  
pp. 1557-1572 ◽  
Author(s):  
John N. Owens ◽  
Marje Molder
Keyword(s):  
Shoot Elongation ◽  
Larix Occidentalis ◽  
Short Shoot ◽  
Bud Development ◽  
Seed Cone ◽  
Long Shoots ◽  
Short Shoots ◽  
Old Trees ◽  
Mother Cells ◽  
Pollen Cone

The time and method of cone-bud differentiation and the phenology of cone-bud development were studied in 10- to 20-year-old trees growing outside their natural range and three 50-year-old trees growing within their natural range.Both pollen-cone and seed-cone buds of western larch (Larix occidentalis Nutt.) normally differentiated on short shoots that were at least 1 year old. Pollen-cone buds were commonly on proximal nonvigorous, often pendant vegetative long shoots in lower regions of the crown, whereas seed-cone buds were usually found on distal short shoots on vigorous but less pendant vegetative long shoots in upper regions of the crown.All potential cone buds were indistinguishable from potential vegetative short shoot buds during bud-scale initiation. In early June, when vegetative short shoots had begun to initiate leaves, cone-bud apices entered a period of differentiation during which time the mitotic frequency of the apices greatly increased followed by a marked increase in apical size. During differentiation, pollen-cone apices did not initiate any basal foliar organs and a short stalk resulted at the base of the cone, whereas seed-cone apices initiated a few basal foliar primordia before bract initiation began. Microsporophyll initiation began during the last half of June and initiation occurred rapidly until the end of July. Micros porangial development occurred from August to late October when fully developed pollen-cone buds became dormant. Pollen mother cells began meiosis before dormancy and overwintered at the diffuse stage. Bract initiation began about the end of June, was rapid until mid-August, then continued more slowly until seed-cone buds became dormant in late October. Ovuliferous scales were initiated acropetally from mid-August until dormancy. Cone-bud differentiation occurred at about the end of the period of vegetative lateral long shoot elongation at all locations.

Interaction between gibberellin A4/7 and root-pruning on the reproductive and vegetative processes in Douglas-fir. IV. Effects on lateral bud development

1986 ◽  
Vol 16 (2) ◽  
pp. 211-221 ◽  
Author(s):  
J. N. Owens ◽  
J. E. Webber ◽  
S. D. Ross ◽  
R. P. Pharis
Keyword(s):  
Normal Development ◽  
Shoot Elongation ◽  
Douglas Fir ◽  
Root Pruning ◽  
Lateral Shoot ◽  
Bud Development ◽  
Lateral Bud ◽  
Mitotic Frequency ◽  
Bud Initiation ◽  
Vegetative Bud

The anatomy, mitotic frequency, size, and total insoluble carbohydrate histochemistry was studied in axillary apices from 9- and 10-year-old Douglas-fir (Pseudotsugamenziesii (Mirb.) Franco) trees after cone induction treatments of root-pruning and (or) stem injections of a gibberellin A4 and A7 (GA4/7) mixture. Axillary buds were initiated at the time of root-pruning, but root-pruning treatment had no effect on axillary bud initiation. Axillary apices from control and gibberellin-treated trees were similar and followed the normal sequence of bud-scale initiation, differentiation, and leaf initiation (described previously) and no cone buds differentiated. Early development of axillary apices from root-pruned and root-pruned, gibberellin-treated trees was normal, but development became retarded near the time of vegetative bud flush. Retarded apices were small with low mitotic frequency and developed many features characteristics of latent apices. Retardation of axillary apices continued until mid-July when normal development resumed and apices differentiated into reproductive buds or vegetative buds, or became latent. The trees in which the greatest retardation of apical development occurred during lateral shoot elongation produced the most cone buds. These results are discussed in relation to hypotheses proposed to explain how cultural and gibberellin treatments affect cone induction in the Pinaceae.

Bud development in mountain hemlock (Tsuga mertensiana). I. Vegetative bud and shoot development

1984 ◽  
Vol 62 (3) ◽  
pp. 475-483 ◽  
Author(s):  
John N. Owens
Keyword(s):  
Growth Cycle ◽  
Shoot Development ◽  
Bud Development ◽  
Vegetative Buds ◽  
Lateral Shoots ◽  
Tsuga Mertensiana ◽  
Terminal Buds ◽  
Lateral Branches ◽  
Relationship Of ◽  
Vegetative Bud

Vegetative buds of mature Tsuga mertensiana (Bong) Carr. (mountain hemlock) were studied throughout the annual growth cycle. Cell divisions began in vegetative buds in mid-April and shoots and leaves elongated within the bud scales causing the buds to burst in late June. Lateral shoots completed elongation by the end of July. Vegetative terminal apices from lateral branches began bud-scale initiation when bud dormancy ended. All bud scales were initiated by the end of July. Leaf primordial initiation occurred from that time until mid-October when vegetative buds again became dormant. Axillary buds were initiated on the elongating shoots in early June then followed the same phenology as vegetative terminal buds. Vegetative bud and shoot development are compared with that of western hemlock and certain other members of the Pinaceae. The relationship of bud development to shoot development is discussed for mountain hemlock and other conifers having a similar pattern of vegetative bud development.

Bud development in mountain hemlock (Tsuga mertensiana). II. Cone-bud differentiation and predormancy development

1984 ◽  
Vol 62 (3) ◽  
pp. 484-494 ◽  
Author(s):  
John N. Owens
Keyword(s):  
Shoot Elongation ◽  
Bud Development ◽  
Seed Cone ◽  
Cone Apex ◽  
Tsuga Mertensiana ◽  
Lateral Branches ◽  
Mother Cells ◽  
Pollen Cone ◽  
Bud Initiation ◽  
Vegetative Bud

Seed cones of Tsuga mertensiana (Bong) Carr. occur terminally on distal lateral branches and form from the differentiation of a terminal, previously vegetative apex, into a seed-cone apex. Pollen cones commonly occur on lateral branches and form from the differentiation of an undetermined axillary apex about 6 weeks after axillary bud initiation. Pollen cones also occasionally occur terminally. All cone buds began differentiation in late July after bud-scale initiation was complete and at about the end of lateral shoot elongation. Seed-cone buds initiated bracts and ovuliferous scales, but not ovules, before they became dormant at the end of October. Pollen-cone buds initiated all microsporophylls by early September. Microsporangia containing microspore mother cells differentiated before pollen-cone buds became dormant in mid-October. The time of cone-bud differentiation is related to vegetative bud and shoot development. The time and method of cone-bud differentiation is discussed in relation to T. heterophylla and other conifers having similar bud development.

Interaction between gibberellin A4/7 and root-pruning on the reproductive and vegetative processes in Douglas-fir. III. Effects on anatomy of shoot elongation and terminal bud development

1985 ◽  
Vol 15 (2) ◽  
pp. 354-364 ◽  
Author(s):  
J. N. Owens ◽  
J. E. Webber ◽  
S. D. Ross ◽  
R. P. Pharis
Keyword(s):  
Shoot Elongation ◽  
Douglas Fir ◽  
Apical Growth ◽  
Root Pruning ◽  
Bud Development ◽  
Leaf Initiation ◽  
Terminal Bud ◽  
Terminal Buds ◽  
Effective Cone ◽  
Vegetative Bud

The relative importance of cell division and cell elongation to shoot elongation and the anatomical changes in vegetative terminal apices were assessed for 9- and 10-year-old seedlings of Douglas-fir (Pseudotsugamenziesii (Mirb.) Franco) in response to two effective cone-induction treatments, gibberellin A4/7 (GA4/7) and root-pruning (RP). Root-pruning was done in mid-April at the start of vegetative bud swelling and GA treatments were begun at vegetative bud flushing in mid-May and continued until early July. Shoot elongation before flushing resulted primarily from cell divisions and was not affected by the RP treatment. Shoot elongation after flushing resulted primarily from cell expansion which was reduced by RP treatments. Root-pruning significantly slowed mitotic activity, apical growth, and development of vegetative terminal buds from mid-June through mid-July. Apical growth then resumed during leaf initiation and the final number of leaf primordia initiated was not affected. This resulted in a delay of 2 to 4 weeks in the transition from bud-scale to leaf initiation. Retarded terminal vegetative apices anatomically resembled latent axillary apices but were never completely inhibited. GA + RP had the same effect as RP. GA4/7 alone had no effect on shoot or apical development. These results show that RP and GA + RP significantly retard shoot elongation and terminal bud development but still allow normal development of vegetative terminal buds. Retardation of bud development by a few weeks shifts the critical morphogenetic phase of transition from bud scale to leaf initiation to a later time when endogenous and environmental conditions may differ from the normal.

Shoot development in Betula papyrifera. I. Short-shoot organogenesis

1983 ◽  
Vol 61 (12) ◽  
pp. 3049-3065 ◽  
Author(s):  
Alastair D. Macdonald ◽  
D. H. Mothersill
Keyword(s):  
Axillary Buds ◽  
Axillary Bud ◽  
Bud Burst ◽  
Betula Papyrifera ◽  
Short Shoot ◽  
Mature Trees ◽  
Shoot Buds ◽  
Female Inflorescence ◽  
Terminal Bud ◽  
Short Shoots

Buds and developing branches of Betula papyrifera were collected weekly from mature trees during three successive growing seasons. Material was prepared to show stages of bud inception, development, and flushing and female inflorescence inception. Short shoots develop from (i) proximal axillary buds on long shoots (ii) short-shoot terminal buds, or (iii) axillary buds on flowering short shoots. An axillary bud apex forms a terminal bud after bud burst. An axillary bud possesses one outer rudimentary leaf, but all other short-shoot buds have three outer rudimentary leaves. All short-shoot buds possess, in addition, one–three embryonic foliage leaves and, distally, three primordial rudimentary leaves which form the outermost appendages of the succeeding terminal bud. Rudimentary leaf stipules form the cataphylls. Foliage leaf primordia are initiated in May – early June and rudimentary leaves arise in late June – July. If a bud apex is initiated in year n, female inflorescence induction occurs in late June of year n + 1 or any succeeding year. An axillary bud develops on a short shoot as a consequence of flowering; it is initiated concurrently with inflorescence development and its development is completed during flowering and seed maturation. Short- and long-shoot buds can be distinguished, upon dissection, in mid-July when buds are forming. Hence, determination of potential long and short shoots occurs the year before bud burst.

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