Abstract:Trees in seasonal climates gauge winter progression to assure vital and productive blooming. However, how dormant plants asses environmental conditions remains obscure. We postulated that it involves the energetic reserves required for bloom, and therefore studied winter carbohydrate metabolism in deciduous trees. We quantified non-structural carbohydrates throughout winter in almond, peach, and pistachio trees in California and Israel and characterized winter metabolism. We constructed a carbohydrate-temperat… Show more
“…4) as evidenced by the stable NSC pools in trunk throughout the year in walnut (Fig. 5) which are also reported in many studies and can be attributed to long-term storage that ensure survival during stress 10,29,32,34,[45][46][47][48][49] . (3) Avoid injuries as collecting cores can lead to stem splitting and fungi infections, as it is known to happen in walnut.…”
Section: Discussion Nsc Seasonal Trend Synchronism and Spatial Gradiementioning
confidence: 65%
“…6), there was always increase in total NSC concentration in twigs that was either maintained (pistachio) or dropped to a lower level (almond, walnut) possibly due to mobilization for metabolism, translocation to roots 35,52 . This accumulation of NSC at leaf abscission is most likely associated with the storage of NSC to ensure winter survival 8,10,32,35,50 .…”
Section: Discussion Nsc Seasonal Trend Synchronism and Spatial Gradiementioning
confidence: 99%
“…NSC storage has seasonal fluctuations marked by the alternation between a favorable season with positive net carbon balance and a dormancy season when trees rely solely on stored NSC 10,12 . Seasonal NSC fluctuation has been reported for trees from various phylogenetic groups (gymnosperms and angiosperms), life habits (deciduous, evergreen), and biomes (Boreal, Temperate, Mediterranean and Tropical) in natural conditions 29,[31][32][33][34][35][36][37] .…”
Despite non-structural carbohydrate (nSc) importance for tree productivity and resilience, little is known about their seasonal regulations and trade-off with growth and reproduction. We characterize the seasonal dynamics of nSc in relation to the aboveground phenology and temporal growth patterns of three deciduous Mediterranean species: almond (Prunus dulcis (Mill.) D. A. Webb), walnut (Juglans regia L.) and pistachio (Pistacia vera L.). Seasonal dynamics of nSc were synchronous between wood tissues from trunk, branches and twigs. Almond had almost identical levels and patterns of nSc variation in twigs, branches and trunks whereas pistachio and walnut exhibited clear concentration differences among plant parts whereby twigs had the highest and most variable NSC concentration, followed by branches and then trunk. While phenology had a significant influence on NSC seasonal trends, there was no clear trade-off between NSC storage and growth suggesting that both were similarly strong sinks for NSC. A temporal trade-off observed at the seasonal scale was influenced by the phenology of the species. We propose that late senescing species experience C allocation trade-off at the end of the growing season because of c-limiting thermal conditions and priority allocation to storage in order to survive winter. Rising temperatures due to global climate change are associated with significant shifts in tree phenology, while the increase in the frequency and intensity of drought events threatens their survival 1-4. The shifts in temperature combined with drought events not only disturb non-structural carbohydrate (NSC, starch and soluble sugars) accumulation in summer but also their remobilization during winter and spring 5-8. As remobilization of stored NSC allows plants to buffer periods of carbon (C) deficit when supply by photosynthesis is not sufficient to sustain maintenance, growth and defense, they play a key role in tree survival through periods of stress and winter dormancy and allow for resumption of growth in spring 9-15. Hence, the disturbance of evolved seasonal patterns of NSC due to climate change may lead to an overall NSC reserve depletion, leaving trees highly vulnerable to mortality 16. As NSC reserve depletion remains debated, another option is that strong C demand of a storage sink could reduce C supply to growth or reproduction, leading to reduction in productivity of natural populations and agroecosystems with dramatic consequences for ecosystems and food production 17-19. It is therefore critical to understand how perennial plants integrate multiannual, seasonal and short-term NSC regulation in response to short-term stress, seasonal environmental signals and long-term global change in order to fully predict and potentially mitigate impact of climate change. The classical view of storage formation as the accumulation of resources when supply exceeds demand is now supplanted by the understanding of storage as a competing C sink 16,20,21. In fact, a classical model of C allocation presented as a static ...
“…4) as evidenced by the stable NSC pools in trunk throughout the year in walnut (Fig. 5) which are also reported in many studies and can be attributed to long-term storage that ensure survival during stress 10,29,32,34,[45][46][47][48][49] . (3) Avoid injuries as collecting cores can lead to stem splitting and fungi infections, as it is known to happen in walnut.…”
Section: Discussion Nsc Seasonal Trend Synchronism and Spatial Gradiementioning
confidence: 65%
“…6), there was always increase in total NSC concentration in twigs that was either maintained (pistachio) or dropped to a lower level (almond, walnut) possibly due to mobilization for metabolism, translocation to roots 35,52 . This accumulation of NSC at leaf abscission is most likely associated with the storage of NSC to ensure winter survival 8,10,32,35,50 .…”
Section: Discussion Nsc Seasonal Trend Synchronism and Spatial Gradiementioning
confidence: 99%
“…NSC storage has seasonal fluctuations marked by the alternation between a favorable season with positive net carbon balance and a dormancy season when trees rely solely on stored NSC 10,12 . Seasonal NSC fluctuation has been reported for trees from various phylogenetic groups (gymnosperms and angiosperms), life habits (deciduous, evergreen), and biomes (Boreal, Temperate, Mediterranean and Tropical) in natural conditions 29,[31][32][33][34][35][36][37] .…”
Despite non-structural carbohydrate (nSc) importance for tree productivity and resilience, little is known about their seasonal regulations and trade-off with growth and reproduction. We characterize the seasonal dynamics of nSc in relation to the aboveground phenology and temporal growth patterns of three deciduous Mediterranean species: almond (Prunus dulcis (Mill.) D. A. Webb), walnut (Juglans regia L.) and pistachio (Pistacia vera L.). Seasonal dynamics of nSc were synchronous between wood tissues from trunk, branches and twigs. Almond had almost identical levels and patterns of nSc variation in twigs, branches and trunks whereas pistachio and walnut exhibited clear concentration differences among plant parts whereby twigs had the highest and most variable NSC concentration, followed by branches and then trunk. While phenology had a significant influence on NSC seasonal trends, there was no clear trade-off between NSC storage and growth suggesting that both were similarly strong sinks for NSC. A temporal trade-off observed at the seasonal scale was influenced by the phenology of the species. We propose that late senescing species experience C allocation trade-off at the end of the growing season because of c-limiting thermal conditions and priority allocation to storage in order to survive winter. Rising temperatures due to global climate change are associated with significant shifts in tree phenology, while the increase in the frequency and intensity of drought events threatens their survival 1-4. The shifts in temperature combined with drought events not only disturb non-structural carbohydrate (NSC, starch and soluble sugars) accumulation in summer but also their remobilization during winter and spring 5-8. As remobilization of stored NSC allows plants to buffer periods of carbon (C) deficit when supply by photosynthesis is not sufficient to sustain maintenance, growth and defense, they play a key role in tree survival through periods of stress and winter dormancy and allow for resumption of growth in spring 9-15. Hence, the disturbance of evolved seasonal patterns of NSC due to climate change may lead to an overall NSC reserve depletion, leaving trees highly vulnerable to mortality 16. As NSC reserve depletion remains debated, another option is that strong C demand of a storage sink could reduce C supply to growth or reproduction, leading to reduction in productivity of natural populations and agroecosystems with dramatic consequences for ecosystems and food production 17-19. It is therefore critical to understand how perennial plants integrate multiannual, seasonal and short-term NSC regulation in response to short-term stress, seasonal environmental signals and long-term global change in order to fully predict and potentially mitigate impact of climate change. The classical view of storage formation as the accumulation of resources when supply exceeds demand is now supplanted by the understanding of storage as a competing C sink 16,20,21. In fact, a classical model of C allocation presented as a static ...
“…Increases in global average temperatures have been welldocumented in the literature, but other characteristics of temperature, like regional and seasonal variability or timing, have been less well studied (Allen and Sheridan 2016;Rogers 2013;Trenberth 1983). Among the different thermal characteristics of climate change, timing is an important issue for many bio-climatological processes, as, e.g., earlier onset of spring/summer or delayed onset of autumn and shortening of winter can have impacts on flowering dates (Sperling et al 2019;Woznicki et al 2019), migratory species (Fraser et al 2019;Helm et al 2019;Schmaljohann 2019), and human adaptation to extreme temperature environments. In this work, we developed a new configuration of the seasons in order to quantify changes in timing in thermal climate characteristics.…”
Previous studies examining climate change and changes in the timing of seasons have used a fixed temperature threshold for season onset. In this study, the timing of seasons was determined using non-fixed threshold methods. Twelve new timing indices were defined to account for shifts in seasons and season onset day, thermal centroid day, and length. The Mann-Kendall test, Theil-Sen's slope estimator, sequential Mann-Kendall test, and least square linear regression were used to assess trends. The timing indices were examined using data from two meteorological stations in Iran with 50 years of records. Spatio-temporal variations in each index over 30 years (1987-2016) were then determined for Khuzestan province in southwestern Iran. Trend analysis for several indices indicated that the timing of seasons had probably changed in the south and west of the study area, while mountainous regions showed non-significant trends. Based on the hottest and coldest 90-day periods (summer and winter, respectively), during the three decades studied, spring lengthened by 5-10 days/decade in the plain region of Khuzestan province and autumn shortened by about 5-8 days/decade. The centroid of winter occurred earlier, by 2-5 days/decade, in the plains area, while the thermal centroid of summer did not change significantly. Overall, the difference between the thermal centroid of winter and summer (C win-sum) in the plains area significantly decreased, by 6-8 days/decade, in the 30-year period.
“…An excessive fruit load in the previous season may affect the C/N relationship, reducing plant reserves, especially in late-ripening cultivars in which the maturation of fruits coincides with flower induction. It can even cause competition among organs for carbohydrates, since final fruit growth immediately precedes flower bud initiation, which is a factor contributing to alternate production in unmanaged fruit trees [91][92][93][94][95][96][97].…”
Here, we reviewed both endogenous and exogenous factors involved in the processes of flower bud formation and flower development in peach, analyzing how they can be affected by climatic change in temperate zones, explored the expansion of peach to tropical or subtropical zones. The process of flower bud formation in peach differs between low winter chilling and temperate conditions. Although the main steps of flower development are maintained, the timing in which each one occurs is different, and some processes can be altered under low winter chilling conditions, with a great impact on fruit production and crop management. Further studies on flower bud induction and differentiation under warmer conditions are fundamental for addressing the alterations in flower bud development that negatively impact on next season’s harvest. In the future, horticulturalists and scientists will face several challenges, mainly how high temperatures affect the expression of the main genes regulating flower formation and how to improve crop management in these conditions.
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