Shoot type demography and dry matter partitioning: a morphometric approach in apple (Malus ×domestica)

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.

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.


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.


1984 ◽  
Vol 62 (3) ◽  
pp. 446-453 ◽  
Author(s):  
J. Cartey Caesar ◽  
Alastair D. Macdonald

Postflush observations on shoots of Betula papyrifera Marsh. indicated that long and short shoots differ in a range of morphological characteristics. Long shoots developed from distal axillary buds and short shoots developed from proximal axillary buds on the previous year's long shoots. Consequently, the potential of a bud to develop into a long shoot decreased basipetally. Potential long-shoot buds had higher bud-relative growth rates, stem-relative growth rates, leaf-relative growth rates, and stem dry weights during the course of postflush growth. Changes in leaf thickness, expressed in terms of specific leaf area and specific leaf weight, indicated that long shoots temporarily had thinner leaves than did short shoots a few weeks after flushing. Net assimilate requirements in long shoots for late leaf and internodal expansion may explain these observations. Nearing maturity, long-shoot early leaves became thicker, possibly owing to greater shoot vigour and (or) higher photosynthetic efficiency. Consequently, mature long-shoot early leaves possessed larger and thicker laminae, longer petioles, more side nerve pairs, and tended to grow more in length than width than short-shoot leaves on shoots of comparable age. Leaves of older short shoots, 2–10 years old, attained a greater size and had longer petioles than those of 1-year-old short shoots. Stem elongation and the development and expression of leaves in long shoots seemed to have a correlative influence on the overall vigour of long shoots.


The various dispersed organs belonging to the Pentoxylon plant viz. Pentoxylon (stem), Nipaniophyllum (leaf), Sahnia (male flower) and Carnoconites (female cone) have been studied in detail. Apart from the long shoots (type 1 shoots), the plant bore three different kinds of short shoots: the thick woody short shoots, each with a broadly conical head (type 2 shoots); the slender parenchymatous short shoots (type 3 shoots); and the slightly thicker parenchymatous short shoot (type 4 shoot) terminating in a Sahnia flower. In addition to the well known Nipaniophyllum raoi leaves a second species, N. hobsonii sp. nov., is recognized. In Sahnia the sporangiophores were borne on a collar-like structure formed by the raised margin of the receptacle. The broadly conical head of the thick woody short shoot (type 2 shoot) might be the basis of the cone-bearing branchlets of Carnoconites fruits. The seeds of Carnoconites are spirally arranged rather than being in longitudinal rows as previously suggested. Pentoxylon was probably a shrubby plant which grew beside water. It sent up erect branched leafy shoots which after a few seasons of growth flopped onto the ground or on other stems, making a thicket. Although the stem, Pentoxylon , resembles Medullosa and Rhexoxylon anatomically, the reproductive parts of the plant, Sahnia and Carnoconites , are unlike those of any group of gymnosperms. The Pentoxylon plant is accordingly regarded as an extinct gymnosperm of unknown affinity. Nipanioxylon guptai has previously been regarded as related to Pentoxylon , but its holotype is believed to be a conifer and has nothing to do with the Pentoxylon plant.


HortScience ◽  
1997 ◽  
Vol 32 (3) ◽  
pp. 506D-506
Author(s):  
W. Alan Erb ◽  
David C. Ferree ◽  
Frank D. Morrison ◽  
Mark Pyeatt ◽  
Richard Ryer

This study was conducted at three locations (Manhattan, Kan.; Wichita, Kan.; Wooster, Ohio) for 3 years (1994–1996). At bloom, 2-year-old limb sections from `Smoothee', `Jonagold', `Empire', and `Rome' on M.9EMLA, Bud 9, Mark, Ottawa 3, or M.26EMLA were evaluated for flowering and vegetative, spurs (5 cm or less), short shoots (5–15 cm) and long shoots (>15 cm). In mid-August, spur quality was estimated by randomly selecting five spurs per cultivar rootstock combination. There were significant location and year differences for all the morphological and spur quality characters measured. Across locations and years, the following characteristics were consistently high for the cultivars listed: stem density of flowering spurs for `Empire'; and leaf area, bud-diameter and average leaf size per spur for `Jonagold'. The most consistently high characteristics across locations and years for the rootstocks were for stem density of flowering spurs for Mark and leaf number, leaf area, bud-diameter, and average leaf size per spur for M.26EMLA. Stem density for flowering short shoots was highest for `Smoothee' and M.9EMLA in Wooster, `Jonagold' and Bud 9 in Wichita and `Rome', `Jonagold', and Bud 9 in Manhattan. Flowering long shoot stem density was highest for `Smoothee', `Jonagold', and M.26EMLA in Wooster, `Smoothee' in Wichita, and `Jonagold' and Ottawa 3 in Manhattan. There were some significant cultivar by rootstock interactions. The most-consistent interactions across locations and years were for stem cross-sectional area, stem length, stem density of flowering spurs, and flowering short shoots and bud-diameter per spur.


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).


1982 ◽  
Vol 12 (4) ◽  
pp. 853-864 ◽  
Author(s):  
J. G. Isebrands ◽  
N. D. Nelson

The branch morphology and the distribution of leaves and specific leaf weight were determined within the crown of 5- and 6-year-old Populus 'Tristis No. 1' (P. tristis Fisch. × P. balsamifera L.) trees grown in northern Wisconsin under short-rotation, intensive culture at 1.2- and 0.6-m square spacings, respectively. The relationship of leaf area to aboveground biomass productivity was also evaluated for the same trees. The first-order branches within the trees exhibited acrotony and were predominantly long shoots. No branching higher than third-order was observed. Leaf size and specific leaf weight were greatest on the current terminal shoot and decreased from the upper portion of the crown to the base. When the 6-year-old trees were divided into eight 1-m vertical strata, over 80% of the total number of leaves and total leaf area was in three middle strata (4–7 m), and most of the 1-m strata contained leaf area attached to two or more height growth increments. Leaves attached to branches on a single height growth increment of the 6-year-old trees occurred in up to four 1-m vertical strata. Long shoots comprised 53% of total leaf area in the 5-year-old trees and 66% in the 6-year-old trees, short shoots the remainder. Ninety-five percent of the long shoots in the 6-year-old trees were in the three uppermost vertical strata (5–8 m), and 95% of the short shoots were in the lowermost leaf-containing vertical strata (3–6 m). Long-shoot leaves had higher specific leaf weights than short-shoot leaves attached to branches on the same height growth increment. Leaf-area indices (LAI) were 7.6 and 8.8 m2•m−2 for the 5- and 6-year-old stands, respectively. Leaf area per tree was linearly related to the aboveground biomass of the tree. The linear regression line for the relationship between leaf area and D2H (diameter2 × height) for the 6-year-old trees in the study was statistically different from that of the 5-year-old-trees. The data presented suggest that this relationship may serve as a useful quantitative index of crown closure in poplar stands. The results also suggest some crown morphological criteria useful for selection and breeding of improved poplar trees for short-rotation intensive culture.


1983 ◽  
Vol 61 (12) ◽  
pp. 3066-3071 ◽  
Author(s):  
J. Cartey Caesar ◽  
Alastair D. Macdonald

Short shoots of Betula papyrifera Marsh, may be vegetative or reproductive. The latter bear a female inflorescence. Early flushing and rapid growth of short-shoot buds depend on the age and position of the short shoot. Axillary short-shoot buds flush later than 2- to 4-year-old short-shoot terminal buds, which in turn flush later than 5- to 10-year-old shoots. Mean relative growth rate (RGR) of 5- to 10-year-old short-shoot buds is greater than that of younger short-shoot buds. It is suggested that older short-shoot buds are relatively autonomous and that the flushing long shoot exhibits an inhibitory influence on the proximal axillary buds and possibly on young short-shoot terminal buds. Reproductive short shoots differ from vegetative short shoots in that they have lower leaf area ratios and leaf RGR, higher specific leaf area, smaller leaf areas, and fewer side nerve pairs and they grow more in length than in width. These findings are related to reproductive cost. The developing inflorescences act as preferred "sinks" for resource allocation.


1988 ◽  
Vol 66 (11) ◽  
pp. 2234-2246 ◽  
Author(s):  
W. R. Remphrey ◽  
G. R. Powell

In saplings of Larix laricina (Du Roi) K. Koch (tamarack), correlations between projected leaf area (PLA) and architectural variables such as shoot length and shoot age were incorporated into existing simulation models to estimate the distribution of PLA in the crown according to several spatial, temporal, and morphological parameters. After five generations of simulated shoot growth, PLA values ranged from 8.2 m2 for trees with short height growth increments (HGIs) and no syllepsis to 25.5 m2 for those with long HGIs and heavy syllepsis. Although PLA increased, the rate of increase declined over time. In early simulated generations, long-shoot PLA predominated. In the fifth simulated generation, short shoots bore about 75% of the PLA. There was a basipetal increase in PLA by HGI, but the relationship was nonlinear. In trees with syllepsis, sylleptic origin branches on individual HGIs carried more PLA than concomitant proleptic branches for 1 year but thereafter the proportions were reversed. Over successive generations, the contribution of different branch orders to the total PLA shifted from mostly first-order long shoots (including PLA on daughter short-shoot axes) to second-order shoots carrying more than 50% by year 5. Because of the short-shoot contribution, there was considerable PLA in all regions of the crown, although the greatest concentration was in lower regions of midconic zones. Simulated PLA index increased substantially with crown development. Trees with short HGIs had the greatest PLA index and those with long HGIs had the least.


1984 ◽  
Vol 62 (4) ◽  
pp. 771-777 ◽  
Author(s):  
G. R. Powell ◽  
Kathleen J. Tosh ◽  
W. R. Remphrey

Trees of Larix laricina (Du Roi) K. Koch reaching the stage of first cone bearing tended to produce the majority of their seed cones, and many of their pollen cones, in lateral (axillary) positions along long shoots. In subsequent cone bearing, a greater proportion of the cones occurred in the typical (for the genus) position terminating short shoots. Some trees 2 to 4 m tall bore over 500 lateral seed cones. Lateral cones occurred on all kinds of long shoots, except sylleptic first-order shoots, produced in the 3-year-old portion of the crown. Lateral seed cones were borne on the morphogenically proximal halves of the long shoots and on all surfaces around the circumference of the shoots, but they were less frequent on upper surfaces than on other surfaces. Lateral pollen cones occurred in the proximal 10% of the lengths of the bearing shoots and were restricted to the undersurfaces or sides of the shoots. Lateral cone buds were distinctively larger and contained more bud scales than adjacent lateral short-shoot buds.


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