scholarly journals Vegetative growth and cluster development in Shiraz grapevines subjected to partial root-zone cooling

AoB Plants ◽  
2013 ◽  
Vol 5 (0) ◽  
pp. plt036-plt036 ◽  
Author(s):  
S. Y. Rogiers ◽  
S. J. Clarke
1989 ◽  
Vol 29 (2) ◽  
pp. 267 ◽  
Author(s):  
GA Buchanan ◽  
GD Godden

Carbofuran, oxamyl, aldicarb and fenamiphos treatments were tested for control of grape phylloxera [Daktulosphaira vitifolii (Fitch)] on ungrafted Cabernet Sauvignon grapevines in central Victoria. All insecticides were applied as granular formulations to the root zone of grapevines. Oxamyl was also tested as a foliar spray. Carbofuran was the most effective treatment, although aldicarb and oxamyl reduced phylloxera populations at some sampling periods. Fenamiphos did not control phylloxera. Vegetative growth, yield and root mass of infested grapevines declined during the 3 years of the experiment. In the third year, carbofuran- treated vines had significantly (P=0.05) greater fruit yield and more vegetative growth than control vines, but were performing poorly in relation to yields expected from uninfested vines. It is concluded that carbofuran treatment combined with optimum viticultural management may delay or reduce the decline of phylloxera infested grapevines. However, replanting with vines grafted to resistant rootstocks is a preferable long-term solution.


HortScience ◽  
1995 ◽  
Vol 30 (3) ◽  
pp. 543-546
Author(s):  
D.M. Glenn ◽  
S.S. Miller

The objectives of this 7-year study were to determine the effect of repeated root pruning and irrigation on peach (Prunus persica L. Batsch) tree growth and soil water use. Root pruning began in the year of planting. Peach trees trained to a freestanding “Y” were root-pruned at flowering for 4 years (1985 to 1988) and subsequently at flowering and monthly through July for 3 years (1989 to 1991). Irrigation was withheld or applied the full season or only during stage 3 of fruit growth on root-pruned and non-root-pruned trees. Root pruning limited soil water availability throughout most of the growing season when irrigation was withheld; however, when irrigation was applied, there was no difference in soil water availability. The root length density of peach roots was greatest in the 0 to 30-cm depth, was promoted by irrigation, and was reduced by root pruning in the 0 to 90-cm root zone. Full-season irrigation increased vegetative growth over the nonirrigated treatments. Root pruning had no effect on vegetative growth measured as fresh pruned material. The treatments had no effect on leaf nutrient content, except that root pruning reduced Zn in five consecutive years. Fruit yield was reduced 1 in 5 years by root pruning, and full-season irrigation reduced yield in 3 of 5 years. Repeated root pruning restricted the lateral spread of the root zone and the use of soil resources, yet on the deep soil of this site, restricting the lateral extent of the root zone did not reduce vegetative tree growth.


2001 ◽  
Vol 70 (6) ◽  
pp. 760-766 ◽  
Author(s):  
Tanjuro Goto ◽  
Noriyuki Takaya ◽  
Naoko Yoshioka ◽  
Yuichi Yoshida ◽  
Yoshihiro Kageyama ◽  
...  
Keyword(s):  

OENO One ◽  
1998 ◽  
Vol 32 (1) ◽  
pp. 1 ◽  
Author(s):  
Nathalie Ollat ◽  
Laurence Geny ◽  
Jean-Pierre Soyer

<p style="text-align: justify;">A method for producing fruiting cuttings of grapevine cv. Cabernet Sauvignon is described. The main developmental features of these cuttings are presented. The clusters reach maturity after 5 months and the period of cluster development is not shortened. Before flowering, a careful control of stem and leaf growth improves the partitioning of stored carbon towards the roots and the cluster. Vegetative growth occurs mainly between fruit set and veraison. During ripening, the leaf to fruit ratio is between 20 and 30 cm<sup>2</sup> of leaf area per gram of fruit. In the cuttings as well as in grapevines from the vineyard, free polyamine content in the leafblade does not change during development. Conjugate polyamine content does not evolve in the same way. It peaks at veraison for vineyard leaves but decreases continuously for cuttings. A proper nutrient solution provides a minerai composition in accordance with viticultural requirements. The cuttings also behave like vineyard plants in response to different levels of potassium in the nutrient solution.</p>


HortScience ◽  
1992 ◽  
Vol 27 (6) ◽  
pp. 683f-683
Author(s):  
Ayman F. Abou-Hadid ◽  
Abo-Elfotouh M. Abd-Alla ◽  
Richard A. Jones

Cucumber plants )Cucumis sativa cv. Beta-al-pha) were grown in a glasshouse in pots of sand with 3 NaCl levels in the nutrient solution (0.40 and 60 mM) and placed in four large water baths controlled at different temperatures (13, 18,23, and 28°C). The increase of NaCl levels decreased the vegetative growth, seed yield, and seed quality, while the increase of root zone temperature up to 23C° increased the vegetative growth, seed yield and quality. Whereas, 28°C showed lower effect than 23°C. Ethylene production and the content of proline and free amino acids were increased with increasing NaCl levels. The increase of root zone temperature till 23°C decreased ethylene production, proline, and free amino acids contents. Zero NaCl (as control) obtained with 23°C root zone temperature appeared to be the best for the over-all growth, seed yield and seed quality of cucumber plants.


2008 ◽  
Vol 146 (6) ◽  
pp. 695-704 ◽  
Author(s):  
SMILJANA GORETA ◽  
VILJEMKA BUCEVIC-POPOVIC ◽  
GABRIELA VULETIN SELAK ◽  
MAJA PAVELA-VRANCIC ◽  
SLAVKO PERICA

SUMMARYWatermelon is a crop with a high water demand and is frequently grown under conditions of higher than normal root-zone salinity. In the present study, seedlings of watermelon (cv. Fantasy, Citrullus lanatus (Thunb.) Matsum & Nakai) were grown either ungrafted or grafted on three rootstocks: Strong Tosa, S1 (both Cucurbita maxima×Cucurbita moschata), or Emphasis (Lagenaria siceraria). All the plants were exposed to an NaCl-induced salinity stress (electrical conductivity, EC=2·2, 4·0, or 6·0 dS/m). The vegetative growth of all the plants substantially reduced after 2 weeks of exposure to 6·0 dS/m; however, growth of the plants grafted on Strong Tosa reduced less than that of the others. The leaf water content and specific leaf area (SLA, m2/g) decreased with an increasing salinity in grafted plants, but not in ungrafted plants. Salinity induced an increase of superoxide dismutase (SOD) activity in grafted plants up to two-fold depending on the rootstock, whereas it had no effect on this enzyme activity in ungrafted plants. Leaf Na+ concentration increased with increasing salinity in ungrafted and S1 grafted plants, whereas there was no significant leaf Na+ accumulation in Emphasis and Strong Tosa grafted plants. Leaf K+ concentration was affected by the rootstock but not by salinity, thus, the ability to keep a high K+/Na+ ratio was achieved mainly by limiting leaf Na+ concentration. The rootstock determined the leaf Cl− accumulation, with lower overall concentrations found if plants were grafted on the S1 rootstock than on Emphasis or ungrafted plants. Salinity significantly decreased the leaf NO3− concentration on Emphasis grafted plants only, while the NO3−/Cl− ratio was reduced in all the rootstocks. The capacity of Strong Tosa to withstand salt stress better than other tested rootstocks was probably due to the ability to induce anatomical adaptation (SLA) and SOD activity in response to salt stress, and also to the efficiency of Na+ exclusion from the shoot.


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