2014
DOI: 10.1016/j.scienta.2014.10.021
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Gibberellic acid and norflurazon affecting the time-course of flavedo pigment and abscisic acid content in ‘Valencia’ sweet orange

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Cited by 20 publications
(11 citation statements)
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“…23 showed that pre-harvest ABA spray regulates fruit color development in Navel orange, whose pigmentation is due to carotenoids, suggesting the involvement of ABA in the regulation of ripening-related processes. However, in Valencia sweet oranges the ABA level in flavedo increases as color develops but ABA did not trigger color break 24 . On the other hand, it has been suggested that ABA would enhance tissue sensitivity to ethylene, whereas exogenous ethylene application stimulates ABA accumulation and expression of the corresponding biosynthesis genes 18,25,26 , indicating that ABA takes part of a complex hormonal interaction in the regulation of non-climacteric fruit maturation.…”
Section: Introductionmentioning
confidence: 81%
“…23 showed that pre-harvest ABA spray regulates fruit color development in Navel orange, whose pigmentation is due to carotenoids, suggesting the involvement of ABA in the regulation of ripening-related processes. However, in Valencia sweet oranges the ABA level in flavedo increases as color develops but ABA did not trigger color break 24 . On the other hand, it has been suggested that ABA would enhance tissue sensitivity to ethylene, whereas exogenous ethylene application stimulates ABA accumulation and expression of the corresponding biosynthesis genes 18,25,26 , indicating that ABA takes part of a complex hormonal interaction in the regulation of non-climacteric fruit maturation.…”
Section: Introductionmentioning
confidence: 81%
“…Peduncle-girdled oranges remained greener compared to control fruit, but GA and ABA remained at high concentrations (Gambetta et al, 2012). Additionally, exogenous ABA did not promote color development (Iglesias et al, 2007), and norflurazon application, an inhibitor of PDS activity, did not affect chlorophyll degradation, although it partially blocked carotenoid biosynthesis, and thus transiently reduced color intensity and ABA concentration in the flavedo (Gambetta et al, 2014).…”
Section: Abscisic Acidmentioning
confidence: 88%
“…Moreover, in peduncle-girdled fruits, which remained green, GA 1 and GA 4 levels remain high, suggesting that the presence of GA in the peel prevents the onset of fruit color change (Gambetta et al, 2012). In this sense, application of GAs is long recognized to delay chlorophyll degradation and carotenoid biosynthesis in citrus fruit (Lewis and Coggins, 1964;Agustí et al, 1981;García Luis et al, 1986;Alós et al, 2006;Gambetta et al, 2014). Moreover, foliar spray of prohexadione-Ca, a GA biosynthesis inhibitor, before color break, enhanced coloration in Navel orange and increased total carotenoid accumulation in the peel (Barry and van Wyk, 2004).…”
Section: Gibberellinsmentioning
confidence: 99%
“…The Promalin Ò and CO 2 treatments affected the chlorophyll content. Promalin Ò treatment decreased chl b while it increased chl a. GA has been previously presented as a delayer of chl degradation (Gambetta et al, 2014;Jordi et al, 1995;Wachowicz et al, 2006) what would be according with our results in chl a but contrary to our findings in chl b. Although cytokinins are able to promote chl biogenesis (Dobr anszki and Mendler-Drienyovszki, 2014) many studies have shown that GA and cytokinin exert antagonistic effects, where cytokinins inhibit the production of GA and promote its deactivation and GA inhibit cytokinin responses (Weiss and Ori, 2007).…”
Section: Discussionmentioning
confidence: 81%