Branch architecture of sagebrush and bitterbrush: use of a branch complex to describe and compare patterns of growth

1991 ◽  
Vol 69 (6) ◽  
pp. 1288-1295 ◽  
Author(s):  
C. J. Bilbrough ◽  
J. H. Richards

The concept of the modularity of plant growth form was incorporated with the fates of buds and used as a framework to describe the typical branch-level developmental morphology of sagebrush (Artemisia tridentata ssp. vaseyana (Rydb.) Beetle) and bitterbrush (Purshia tridentata (Pursh) D.C.). Typical branches included one 2-year-old long shoot and all 1-year-old long shoots originating from that twig. Growth patterns were examined by position along each long shoot within the experimental branches. Shoot fates were recorded for each node and biomass production was estimated. Both species had specific locations where vegetative long shoot production was higher than any other location within the experimental branches. Sagebrush had an overall linear (excurrent) growth form, with the leader long shoot much larger than lateral long shoots. Sagebrush produced many lateral long shoots and few short shoots. In contrast, bitterbrush had a branched (decurrent) growth form, with few long shoots and many short shoots. The leader rarely grew and was no larger than laterals. Knowledge of the location, frequency, and size of vegetative long shoot production within a branch complex provides an understanding of the repeated structure of plants. The branch-level approach provides the information necessary before the effects of environmental factors on growth patterns can be determined. Key words: Artemisia tridentata ssp. vaseyana (Rybd.) Beetle, branch architecture, bud fates, developmental morphology, Purshia tridentata (Pursh) D.C., shrub.

1991 ◽  
Vol 21 (10) ◽  
pp. 1475-1480 ◽  
Author(s):  
Brayton F. Wilson

Lengths of all parent and current shoots were measured on three 8- to 10-year-old black birch (Betulalenta L.) trees with branches <8 years old. Older branches had more short shoots (<1 cm long) and shorter long shoots (>2 cm long) than younger branches. Parent long shoots produced three to nine basal short shoots. Observations on short-shoot production were consistent with the hypothesis that only buds with adequate nutrition formed long shoots. Three growth rules were developed for a model that simulated individual branch growth: (i) a regression predicting lateral shoot number from each parent shoot length; (ii) probabilities for the number of short shoots produced by a parent shoot based on the total number of current shoots produced per parent shoot; (iii) a regression predicting current shoot length from parent shoot length, current shoot position (longest to shortest), branch age, and main-axis elongation in the current and previous year. Simulations of 81 branches using these rules predicted shoot numbers and total shoot lengths close to those of the actual branches (R2 = 0.73–0.84).


2004 ◽  
Vol 82 (9) ◽  
pp. 1393-1401 ◽  
Author(s):  
Masae Ishihara ◽  
Kihachiro Kikuzawa

We tested whether the difference in shoot production patterns of reproductive and vegetative shoots is only due to resource or meristem availability or also due to species-specific factors. Rates of shoot production by four shoot types (reproductive long shoots, vegetative long shoots, reproductive short shoots, and vegetative short shoots) in Betula platyphylla Sukatchev var. japonica (Miq.) Hara, Betula davurica Pall., Betula ermanii Cham., Betula grossa Sieb. et Zucc., and Betula maximowicziana Regel were compared. In the first three species, each shoot type produced all four shoot types. However, in the latter species, limited shoot production pathways were found both in reproductive shoots and in vegetative shoots, which do not carry any costs associated with reproduction. Furthermore, shoot production by reproductive shoots was not always diminished, but rather was enhanced compared with that by vegetative shoots in B. maximowicziana. These results suggest the importance of species-specific patterns in shoot production, in addition to previously suggested explanations involving resource or meristem limitation.Key words: species specificity, cost of reproduction, Betula, reproductive shoots, vegetative shoots.


1967 ◽  
Vol 45 (9) ◽  
pp. 1643-1651 ◽  
Author(s):  
J. Johanna Clausen ◽  
T. T. Kozlowski

Tamarack (Larix laricina (DuRoi) K. Koch) produces long shoots which bear two kinds of needles. Early needles are present in the bud and elongate rapidly after budbreak. Late needles, few of which are present in the bud, elongate later than early needles. Short shoots bear early needles only, and stem length seldom exceeds 1 mm. Seasonal changes in length and weight of needles and stems of both shoot types were measured. In long shoots, 75% of stem elongation, more than 70% of stem weight increment, and 65–70% of late needle elongation occurred after early needles were full-sized. Stem and late needle elongation ceased simultaneously, after which time needle weight decreased and stem weight increased. Early needles probably drew on food reserves while developing, and then themselves contributed to stem and late needle elongation. Final stem weight increase probably used photosynthate from both late and early needles of the current year.Shading of current and last year's needles showed that shoots in which photosynthesis was interrupted in this way produced shorter, lighter-weight stems than did control shoots.


Botany ◽  
2010 ◽  
Vol 88 (11) ◽  
pp. 995-1005 ◽  
Author(s):  
Kenichi Yoshimura

Rhododendron reticulatum D. Don ex G.Don is a common understory shrub in western Japan that exhibits highly plastic crown architecture and occurs in various light environments. I investigated how functional differentiation and spatial distribution of long and short shoots contribute to the plasticity of crown architecture of R. reticulatum. Crown form was derived from the crown depth/width ratio. Crown depth/width ratio was higher in sun-lit crowns. In crowns with higher depth/width ratio, long shoots were distributed in upper positions of the crown. Long shoots grew vertically and horizontally. In crowns with lower depth/width ratio, long shoots were arranged in the outer position of the crown and grew outward. Within neighboring shoots, long shoots had less mass than their paired short shoots. Results suggest that long shoots of R. reticulatum function to expand the crown and to reduce leaf overlap in multilayer crowns, which are found in high-light environments, while both long and short shoots function to minimize leaf overlap in monolayer crowns, which are found in shaded environments. Plasticity of crown architecture by altering shoot position and shoot morphology allows growth under various light environments in the forest understory.


1970 ◽  
Vol 48 (10) ◽  
pp. 1801-1804 ◽  
Author(s):  
D. F. W. Pollard

Different shoot types in aspen crowns carried leaves of different ages; leaders continued to produce leaves until early August and always carried some young leaves, whereas short shoots completed development by mid-June. Development of foliage on long shoots was intermediate between that on leaders and short shoots. Leaf area index of the 6-year-old stand reached a maximum of 2.4, of which 2.1 was contributed by short-shoot foliage. The rest was formed by leaders and long shoots. Young leaves on leaders and long shoots were not sufficient to influence total production in the stand appreciably, even though young aspen leaves may have high photosynthetic efficiencies. These young leaves could, however, influence height growth and lateral development of the canopy.


2001 ◽  
Vol 79 (11) ◽  
pp. 1270-1273 ◽  
Author(s):  
Pierre-Éric Lauri ◽  
Jean-Jacques Kelner

In a study of the apple (Malus ×domestica Borkh.) canopy structure, 5-year-old 'Fuji' and 'Braeburn' trees grafted on a low-vigour rootstock (M9) were compared at both fruiting branch and shoot levels. Percentages of short ([Formula: see text]5 cm) shoots and short shoot leaf area were significantly higher on 'Braeburn' than on 'Fuji', (76.8% vs. 72.6% and 46.9% vs. 42.9% for 'Braeburn' and 'Fuji', respectively). This high percentage of short shoots as compared with literature data was probably due to the training method, which reduced vigour. At shoot level, the ratio between dry masses of axis and leaf, called the axialization index, was determined to compare short and long shoots. Axialization values were higher for 'Braeburn' than for 'Fuji'. Although overall and individual leaf area was greater on long shoots, long shoot axialization (0.64 and 0.54 for 'Braeburn' and 'Fuji', respectively) was approximately twice that of short shoots (0.36 and 0.24, respectively). Therefore, for short shoots, the reduced carbon investment in supporting tissues may explain the significant role short shoots played in supporting early fruit development. For long shoots, the longer time required to reach the autotrophic and then exporting stage as well as the detrimental effect of early extension shoot development on fruit set might be explained by greater axialization.Key words: long shoot, short shoot, axialization index, apple, Malus ×domestica, biomass partitioning.


1987 ◽  
Vol 65 (2) ◽  
pp. 268-279 ◽  
Author(s):  
W. R. Remphrey ◽  
G. R. Powell

Quantitative analysis and simulation modelling of Larix laricina (Du Roi) K. Koch branches revealed a complex system of architectural patterns and correlations. Numbers of lateral buds and long shoots were positively correlated with parent-shoot length, but the relationships varied among shoot orders and for sylleptic shoots. For order 2 and sylleptic shoots, numbers of lateral long shoots were also correlated with associated terminal-shoot lengths. Sylleptic shoots produced more lateral long shoots than equivalent proleptic shoots. Lateral long-shoot lengths decreased basipetally and were correlated with terminal-shoot lengths. Lengths of order 2 lateral long shoots also varied independently with crown position. Generally, the degree of apical control decreased and the proportion of short shoots increased with positions of less vigour in the crown. Terminal long-shoot lengths varied with parent-shoot length, location, and to some extent parent-axis leader length. Terminal short-shoot production was associated with shorter parent shoots. Shorter order 2 shoots (<60 mm) and most order 3 shoots produced no lateral long shoots. The net result was that branch structural development ceased in less vigorous crown positions. The spatial disposition of shoots, as defined by elevation and divergence angles, varied with position of origin around and along parent shoots. Although variable, elevation angles decreased and divergence angles increased basipetally.


1966 ◽  
Vol 44 (12) ◽  
pp. 1623-1632
Author(s):  
L. S. Marchand ◽  
Alastair McLean ◽  
E. W. Tisdale

The behavior of Artemisia tridentata ssp. tridentata and A. tridentata ssp. vaseyana in uniform gardens at Kamloops, Nickel Plate, and Greenstone as well as in some natural habitats supported the separation of the two subspecies. Kamloops (1140 ft) is located in the typical habitat of ssp. tridentata and Nickel Plate (5600 ft) represents the typical habitat of ssp. vaseyana.In their natural habitats ssp. vaseyana flowered about 2 weeks earlier than ssp. tridentata and their flowering periods did not overlap. In the Kamloops uniform garden ssp. vaseyana collections showed two distinct flowering patterns considered to be two ecotypes. The ssp. tridentata collections from the outer edge of the distribution of the subspecies flowered 1 week earlier than collections from the center of the range.Most of the ssp. tridentata plants set out in the Nickel Plate garden died within 3 years but most survived in the one at Greenstone. Almost one-half of the plants of ssp. vaseyana died in the Kamloops garden, mostly during the summers, except for the Nickel Plate material, which appeared more hardy. About 40% of the United States ssp. tridentata killed out in the local tridentata environment (Kamloops), mostly over winter.Leaves of ssp. vaseyana plants were typically wider than those of ssp. tridentata but leaf lengths were variable and not a good diagnostic character. The ssp. vaseyana plants had a spreading-decumbent growth form while ssp. tridentata plants grew more upright.


Author(s):  
L. Szalay

The phenological processes of flower bud development of stone fruits during dormancy are not thoroughly known. The yield of these species, especially of almond, apricot and peach is determined basically by dormancy of flower buds, the survival rate of buds during winter frosts and by their ability to develop normal floral organs in the next spring. After the initiation of floral primordia, flower bud development is taking place in continuous space until blooming, though at different speed characteristic to the species. To study flower bud development during dormancy we applied two alternative methods in different genotypes of almond, apricot and peach: (1) examination of pollen development (microsporogenesis), and (2) the measurement of pistil length. The samples were collected from the central part of Hungary during the dormancy period of 2004/2005. The three fruit species differed significantly in the speed of flower bud development, it was the quickest in almond, followed by apricot and peach. In addition to the species, there were significant differences in the process of microsporogenesis and pistil development between genotypes within species and also between the different types of shoots on which the buds were located. On short shoots buds developed at a higher speed, than on long shoots. Based on our observations, on the short shoots the period of endodormancy was shorter with 5-30 days, according to genotypes, compared to the long shoots. This difference, however, decreased to 2-3 days by the time of blooming.


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