The negative effects of fruit production during one cycle on reproduction during the following cycle are generally explained by two complementary processes: hormone synthesis and carbohydrate mobilization. Our study focused on mango (Mangifera indica L.) for which it has been shown that reproduction decreases and delays vegetative bud outgrowth. This, in turn, affects flowering and fruiting in the following cycle. Vegetative growth therefore plays a pivotal role in irregular fruit production patterns across consecutive years. Our aim was to decipher the respective roles of hormones and carbohydrates on the negative effects of reproduction on vegetative growth. We analyzed the changes in various hormone (auxin, cytokinin, abscisic acid) and carbohydrate (glucose, sucrose, starch) concentrations in terminal axes with vegetative and reproductive fates of two mango cultivars, Cogshall and José, characterized by different bearing patterns, across consecutive phenological periods during a growing cycle. Auxin concentrations were high in inflorescences, fruit peduncles and axes bearing inflorescences or fruit, suggesting auxin-induced inhibition of vegetative bud outgrowth in the flowering and fruiting axes. Moreover, growing fruits, which are strong sink organs, depleted carbohydrates from non-fruiting axes. During vegetative growth, this starch depletion probably contributed to decreasing the probability of and to delaying vegetative bud outgrowth of reproductive axes for Cogshall, and of reproductive and nonreproductive axes for José. Starch dynamics in quiescent and flowering growth units during early fruit growth and their starch concentrations at fruit maturity differed between the two cultivars, presumably in relation to the observed contrasted crop loads and/or to differences in photosynthetic capacity or carbohydrate allocation. These differences between the two cultivars in terms of starch concentration in terminal axes during vegetative growth could partly explain their different bearing patterns.
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http://dx.doi.org/10.1093/treephys/tpab079 | DOI Listing |
Plant Cell Environ
January 2025
Laboratory of Fruit Tree Biotechnology, College of Horticulture, Nanjing Agricultural University, Nanjing, China.
Ecol Evol
December 2024
Holden Arboretum Kirtland Ohio USA.
As plants continue to respond to global warming with phenological shifts, our understanding of the importance of short-lived heat events and seasonal weather cues has lagged relative to our understanding of plant responses to broad shifts in mean climate conditions. Here, we explore the importance of warmer-than-average days in driving shifts in phenophase duration for spring-flowering woodland herbs across one growing season. We harnessed the combined power of community science and public gardens, engaging more than 30 volunteers to monitor shifts in phenology (documenting movement from one phenophase to the next) for 198 individual plants of 14 species twice per week for the 2023 growing season (March-October) across five botanic gardens in the midwestern and southeastern US.
View Article and Find Full Text PDFInt J Mol Sci
December 2024
Institut Agro, Univ Angers, INRAE, IRHS, SFR QuaSaV, 49000 Angers, France.
The source-sink relationship is critical for proper plant growth and development, particularly for vegetative axillary buds, whose activity shapes the branching pattern and ultimately the plant architecture. Once formed from axillary meristems, axillary buds remain dormant or become active to grow into new branches. This transition is notably driven by the regulation of the bud sink strength, which is reflected in the ability to unload, metabolize and store photoassimilates.
View Article and Find Full Text PDFDNA Res
December 2024
Graduate School of Agriculture, Kyoto University, Kyoto 606-8502, Japan.
Bud dormancy is a vital physiological process in woody perennials, facilitating their adaptation to seasonal environmental changes. Satisfying genotype-specific chilling requirements (CR) and heat requirements (HR) through exposure to specific chilling and warm temperatures is essential for dormancy release and the subsequent resumption of growth. The genetic mechanisms regulating bud dormancy traits in Prunus mume remain unclear.
View Article and Find Full Text PDF3 Biotech
December 2024
Morphogenesis and Reproductive Biology of Plants Laboratory, Department of Biological Sciences, University Campus, "Luiz de Queiroz" College of Agriculture, University of São Paulo (ESALQ/USP), 11, Pádua Dias Ave., POB 9, Piracicaba, SP 13418-900 Brazil.
Micropropagation is an important tool for the propagation for recalcitrant species, like This is a first reported about a complete study of the , it includes the vegetative rescue protocol of mature trees, its micropropagation up to the implementation of a mini-garden and clonal micro-garden and evaluation of adventitious rooting of their propagules. The in vitro rejuvenation of genotypes (03, 05, 06, 13 and 15), over 21 successive subcultures, was evaluated by comparing minicutting and microcutting techniques and the efficiency of this biotechnological tool for cloning of the mature trees. The results provide evidence of the in vitro rejuvenation occurring in the mature trees during micropropagation, leading to increases in the multiplication ratios of the microstumps of three genotypes (03, 05 and 15).
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