2000
DOI: 10.1023/a:1006207614388
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Cited by 25 publications
(9 citation statements)
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“…Interestingly, we have previously demonstrated that the exogenous pre-bloom application of GA 3 inhibited berry growth in seeded ‘Kyoho’ and ‘Red Globe’ cultivars, yet stimulated berry growth in ‘Thompson Seedless’ [17]. Similarly, it has also been shown that berry growth was inhibited in the seeded grape cultivar ‘Emperador’ and promoted in the seedless cultivar ‘Emperatriz’ upon GA 3 application [22]. Therefore, we supposed that whether the exogenous pre-bloom application of GA 3 to grape inflorescences stimulates berry production may be cultivar-dependent.…”
Section: Discussionmentioning
confidence: 99%
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“…Interestingly, we have previously demonstrated that the exogenous pre-bloom application of GA 3 inhibited berry growth in seeded ‘Kyoho’ and ‘Red Globe’ cultivars, yet stimulated berry growth in ‘Thompson Seedless’ [17]. Similarly, it has also been shown that berry growth was inhibited in the seeded grape cultivar ‘Emperador’ and promoted in the seedless cultivar ‘Emperatriz’ upon GA 3 application [22]. Therefore, we supposed that whether the exogenous pre-bloom application of GA 3 to grape inflorescences stimulates berry production may be cultivar-dependent.…”
Section: Discussionmentioning
confidence: 99%
“…The exogenous pre-bloom application of gibberellic acid (GA 3 ) to grapevine, which is an economically important crop that has long been an important component of the human diet, is commonly used to induce seedlessness [17,18], establish early ripening [19], and enhance berry size in seedless cultivars [20-22]. However, despite its importance in viticulture, the precise mechanism by which GA elicits these complex outcomes remains elusive.…”
Section: Introductionmentioning
confidence: 99%
“…Unlike seeded grapevine ( Vitis vinifera L.) cultivars, which have considerably high endogenous GA levels (Lavee, 1960; Kato et al, 1998; Agüero et al, 2000; Perez et al, 2000), berries of the usually small, stenospermocarpic varieties contain low GA quantities since they carry only seed traces, as a result of endosperm abortion following fertilization which leads to cessation of seed development (Iwahori et al, 1967; Cheng et al, 2013). GA application is therefore routinely used to stimulate stenospermocarpic berry development to a commercially acceptable size, and also for rachis stretching and cluster thinning (Weaver, 1958, 1965; Harrell and Williams, 1987).…”
Section: Introductionmentioning
confidence: 99%
“…GA application is therefore routinely used to stimulate stenospermocarpic berry development to a commercially acceptable size, and also for rachis stretching and cluster thinning (Weaver, 1958, 1965; Harrell and Williams, 1987). Issues of differential varietal responsiveness to such GA application have been reported in berries and other vegetative tissues/organs, including rachis and shoot (Weaver, 1958; Hagiwara et al, 1980; Mullins et al, 1992; Agüero et al, 2000). For example, while ‘Thompson seedless’ (TS) berries, required 3–4 applications of 30–45 μM of GA for a twofold increase in size (Dreier et al, 1998), application of 290 μM of GA 3 increased ‘Emperatriz’ berry size by only 20% (Agüero et al, 2000).…”
Section: Introductionmentioning
confidence: 99%
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