Growth Characteristics of Vitis Vinifera L. Cv. Cape Riesling A

Growth Characteristics of Vitis Vinifera L. Cv. Cape Riesling A

Growth Characteristics of Vitis vinifera L. cv. Cape Riesling A. C. DE LA HARPEa, AND J. H. VISSERb (a) Viticultural and Oenological Research Institute, Private Bag X5026, 7600 Stellenbosch, Republic of South Africa. (b) Department of Botany, Univ. Stellenbosch, 7600 Stellenbosch, Republic of South Africa. Date submitted: September 1984 Date accepted: ~nuary 1985 . Keywords: Topping, growt( Vitis The effect of topping on the growth behaviour of Vitis vinifera L. cv. Cape Riesling vineyard was investigated. Shoot and leaf growth of both topped and untopped vines, can be described as sigmoidal. Shoot (cm) and leaf growth (cm') of the topped vines were significantly more than that of the untopped vines and are attributed to lateral shoot growth. Topping had no effect on bunch development. The development of skin, pulp and seed of both topped and untopped vines expressed as a percentage dry mass per berry can be described by a hyperbolic function for the skin, linear for the pulp and parabolic for the seed. Growth has been defined as "the advancement towards of topping on the growth characteristics of Vitis vinifera or attainment of full size or maturity; development: a L. cv. Cape Riesling. gradual increase in size and the process whereby plants and animals increase in size by taking in food" (Bidwell, 1974; Salisbury and Ross, 1978). Growth may be evaluated MATERIAL AND METHODS by measurements of mass, length, height, surface area or volume (Noggle and Fritz, 1976). Growth curves of plants Material: V. vinifera cv. Cape Riesling vines were selected are generally sigmoi"dal (Bidwell, 1974; Noggle and Fritz, as described by de la Harpe & Visser (1983). 1976; Salisbury and Ross, 1978) although double and Methods: The selected vines were divided into two groups triple sigmoi"ds have been reported (Pratt and Reid, 1974; of 104 vines each. One section was topped by removing Coombe, 1976). Sigmoi"ds and double sigmoi"ds have been the apical 30cm of each shoot of the vine at pea berry size described for shoot growth and berry development for (56 days after bud break). For the purpose of this inves­ Vitis spp. and cultivars (Coombe 1960; 1973; 1976; 1980; tigation bud break was defined as that stage at which 10 % Nitsch et al., 1960; Hale, 1968; Harris, Kriedemann and of the shoots had two leaves. Topping was done at pea Possingham, 1968; Coombe and Hale, 1973; Kliewer and berry size to ensure that the treatment was applied before Schultz, 1973). the rapid growth phase of the shoot. The other group was Removal of the apical 25 cm or more of the growing left untapped. Ten topped and 10 untapped vines were shoot tip is called topping (Winkler, et al., 1974) and is randomly selected and on each the two shoots on the normally recommended to inhibit growth of vigorously second spur of each cordon were used for determination growing shoots and to induce uniform and upright growth of shoot length and leaf area. Shoots lengths and leaf (Theron, 1944). By removing 25 cm of the shoot tip, areas were determined frequently at irregular time inter­ apical dominance is removed, resulting in the develop­ vals. Leaf areas were determined with a model LI-3000 Li­ ment of lateral shoots. Cor Portable Area Meter. Four bunches on shoots of the Results obtained in the northern hemisphere indicate second spur of both cordons of three topped as well as that the juvenile leaves of the lateral shoots are the major three untapped vines were sampled 69, 76, 82, 92, 97, 110, sinks for nutrients (Hale & Weaver, 1962; Koblet, 1977) 117, 131, 138, 145 and 152 days after bud break. These but after two to three leaves have matured, basipetal bunches were taken from vines not used for growth translocation of nutrients takes place (Koblet & Perret, measurements. 1971; 1972). After all the berries were removed from 12 bunches of It is important that only vigorously growing vines should the topped and untapped vines sampled at 69, 76, 82, 92, be topped because poor growth will be further aggravated 97, 110, 117, 131, 138, 145 and 152 days after bud break by the effect of topping (Malan, 1935; Theron, 1944). The the berries were mixed and 60 berries were used to deter­ timing and severity of topping are very important because mine the berry volume by water displacement in a measu­ the removal of photosynthetically active leaves at the ring cylinder. The fresh and dry mass of the berry, skin, wrong time will result in insufficient grape nourishment. pulp and seed were determined on these 60 berries. Dry Le Roux & Malan (1945) and Coombe (1959) reported mass was determined by drying at 80°C to a constant that repeated topping (three to four times or more during mass. one season) decreased berry mass. Similarly El-Zeftawi & One way anal~ses of variance wer:e done and regression Weste (1970) found that a drastic decrease in leaf area analyses by a linear Least Squares Curbe fitting programme usually causes a loss in berry mass and sugar concentra­ (Wood & Gorman, 1971). tion. Since 1945 no research work on the effect of topping on the vine was reported in South Africa. It is therefore RESULTS AND DISCUSSION important that the effect of topping on the vine under South African climatic conditions should be investigated. The vegetative growth phase: The aim of this investigation was to determine the effect Shoot growth: The mean, total shoot length for the The authors wish to express their appreciation to Miss. C Nisbet and A. Lourens for technical assistance and Mr. L. Hoffman for data processing and interpretation. S. Afr. J. Enol. Vitic., Vol. 6. No. 1 1985 2 Growth Characteristics of Vitis vinifera untopped vines was 267,8 cm (Fig. 1). Shoot growth started off with a slow elongation rate but the rate 40 increased from 60 days after bud break i.e. shortly after ___TOPPED t topping (Fig. 2). This sharp increase lasted about three VINES days after which the growth rate dropped to approxi­ __UN TOPPED mately three cm per day and declined steadily until no I,_ elongation could be measured at 135 days after bud 3: 0 break. Ci 20 ·; The mean, total shoot length of the topped vines was 410 cm (Fig. 1) which is significantly more than that of the •r-·i I I untopped vines mainly as a result of lateral shoot I I development. The tendency of the growth curve (Fig. 1) of __ JI the topped vines was almost identical with that of untopped vines. Five days after topping the elongation rate increased significantly and reached 37 cm day-' for two days aft.er which it declined sharply to about three cm 50 l 0 15 day' (Fig. 2). Shoot growth of the topped vines stopped T H 155 days after bud break in contrast to the 135 days of the TIME (DAYS AFTER BUD BREAK) untopped vines (Fig. 2). FIG. 2 The growth curve of the untopped vines reported here Daily shoot elongation for topped and untapped Vitis vinifera L. cv. is very similar to those obtained by Van der Westhuizen Cape Riesling vines. (ti significant differences (P :;;:; 0,05)) in the data (197 4), W inkier et al., (197 4) and Zell eke & Kliewer set. (T = Time of topping, H = Harvest). (1979). Leave growth: A total number of 129 leaves per shoot had differentiated on the untopped vines (Fig. 3). A mean of The total leaf area of 4728 cm2 per shoot for the 194 leaves per shoot for topped vines was obtained 134 untopped vines was significantly less than the 7741 cm2 days after bud break which amounted to a significant for the topped vines (Fig. 5). The pronounced burst in increase of 65 leaves over that of untopped vines. shoot growth (Fig. 2) after topping seams to coincide with 450 the decrease in leaf area expansion. 0 200 D 400 D 0 0 350 ~ "' 'i ffi u a.. 15 ~ 300 ,_ w () "'> <( w ~ ~ II 0 250 0 0 I II "' ffi z "':i: ::> l <( 200 z ~ z ~ :i: 150 50 100 50 50 100 15 H T H TIME(DAYS AFTER BUD BREAK) TIME (DAYS AFTER BUD BREAK) FIG. 1 FIG. 3 Fitted curves and observed shoot growth data for topred (0) and Fitted curves and observed number of leaves data for topped (0) and untopped (II) Vitis vinifera L. cv. Cape Riesling vines .. (T = Time of untopped (II) Vitis vinifera L. cv. Cape Riesling vines. (T = Time of topping, H = Harvest). topping, H = Harvest). S. Afr. J. Eno!. Vitic., Vol. 6. No. 1 1985 Growth Characteristics of Vitis vinifera 3 9000 50 D D R2- 0.96 D 7000 •R2-0.95 400 "':i:: D ~ >-- ____ TOPPED 0 0 I Prob. to i I~ 0.05 !VINES D __ UN TOPPED • "' D '"O , .!!' • "'w I Q. 5000 ,'/ uz 30 < ii? I w 11R 2-0.79 , ,: "'< I I I I < • I w / I 300 / D z / < • / 0 / ~ /D / D {J • 1000 D • • D • T H TIME(DAYS AFTER BUD BREAK) 50 100 15 FIG. 4. T H Tl ME (DAYS AFTER BUD BREAK) Fitted curves and observed leaf area data for the average increase in leaf FIG. 6. area from bud break to harvest for topped (0) and untopped (I() Vitis Fitted curves and observed data for the increase in mean fresh mass of 12 vinifera L. cv. Cape Riesling vines. (T = Time of topping, H = the bunch from pea berry size to harvest for topped (0) and untopped Harvest). (I() Vitis vinifera L. cv. Cape Riesling vines. (T = Time of topping, H = Harvest).

View Full Text

Details

  • File Type
    pdf
  • Upload Time
    -
  • Content Languages
    English
  • Upload User
    Anonymous/Not logged-in
  • File Pages
    6 Page
  • File Size
    -

Download

Channel Download Status
Express Download Enable

Copyright

We respect the copyrights and intellectual property rights of all users. All uploaded documents are either original works of the uploader or authorized works of the rightful owners.

  • Not to be reproduced or distributed without explicit permission.
  • Not used for commercial purposes outside of approved use cases.
  • Not used to infringe on the rights of the original creators.
  • If you believe any content infringes your copyright, please contact us immediately.

Support

For help with questions, suggestions, or problems, please contact us