• Energy Research

International audience

AbstractEvaluation of chilling requirements (CR) of cultivars of temperate fruit trees provides key information to assess regional suitability, according to winter chill, for both industry expansion and ongoing profitability as climate change continues. Traditional methods for calculating CR use climate controlled chambers and define CR using a fixed budburst percentage, usually close to 50% (CR-50%), without considering the productivity level associated to this percentage. This CR-50% definition may underestimate the real CR of tree crops for optimal productivity. This underestimation is particularly important to consider as winter chill accumulation is declining in many regions due to climate change. In this work we used sweet cherry to analyse the traditional method for calculating CR in many Rosaceae species (CR-50%) and compared the results with more a restrictive, productivity focused method, with CR defined with a 90% bud break level (90%, CRm-90%) close to the optimal budburst which assures productivity. Climate projections of winter chill suitability across Europe using CR-50% and CRm-90% were calculated. Regional suitability landscape was highly dependent on the method used to define CR and differences were found for a wide area of the European geography, both cold and mild winter areas. Our results suggest a need to use an optimal budburst level for the assessment of CR for sweet cherry. The use of traditional methods to determine CR can result in an underestimation of productivity CR with negative consequences for the fruit industry, particularly as climate change advances.

Summary The present study investigated the genetic determinism of flowering date (FD), dissected into chilling (CR) and heat (HR) requirements. Elucidation of the genetic determinism of flowering traits is crucial to anticipate the increasing of ecological misalignment of adaptative traits with novel climate conditions in most temperate‐fruit species. CR and HR were evaluated over 3 yr and FD over 5 yr in an intraspecific sweet cherry (Prunus avium) F1 progeny, and FD over 6 yr in a different F1 progeny. One quantitative trait locus (QTL) with major effect and high stability between years of evaluation was detected for CR and FD in the same region of linkage group (LG) 4. For HR, no stable QTL was detected. Candidate genes underlying the major QTL on LG4 were investigated and key genes were identified for CR and FD. Phenotypic dissection of FD and year repetitions allowed us to identify CR as the high heritable component of FD and a high genotype × environment interaction for HR. QTLs for CR reported in this study are the first described in this species. Our results provide a foundation for the identification of genes involved in CR and FD in sweet cherry which could be used to develop ideotypes adapted to future climatic conditions.

Walnut trees are grown worldwide for their edible fruits, which have high nutritional value. To address climate change, researchers have studied walnut phenology to create cultivars adapted to warmer climates. The objective of this study is to propose a scale for phenological Persian walnut observations using the Biologische Bundesanstalt, Bundessortenamt, und CHemische Industrie (BBCH) codification and alignment with historical alphameric scales. Here, the principal growth stages (PGSs) of Persian walnut (Juglans regia L.) are described using stages from a previously available alphanumeric scale. This standardised phenological scale describes Persian walnut growth from the dormant vegetative state through reproductive budding and senescence. This phenological scale is expected to increase the efficiency of walnut phenological monitoring. Fifty-seven stages are used to describe the life cycle of Persian walnut in this BBCH scale. Of these 57 stages, 3 stages are dedicated to seed germination (PGS-0), 4 stages are dedicated to bud development (PGS-0), 7 stages are dedicated to leaf development (PGS-1), 4 stages are dedicated to stem elongation (PGS-3), 8 stages are dedicated to inflorescence emergence (PGS-5), 5 stages are dedicated to male flowering (PGS-6), 5 stages are dedicated to female flowering (PGS-6), 5 stages are dedicated to fruit development (PGS-7), 12 stages are dedicated to fruit ripening (PGS-8), and 4 stages are dedicated to leaf senescence (PGS-9).

Perennial fruit crops phenology such as cherry is an ideal bio-indicator of climate change due to their long-lasting features, in particular, dates of flower opening and full bloom. This implies i) the use of several generations of cherry trees/ orchards and ii) the use of the same original cherry cultivars, which existed as bearing trees and were replanted after the orchard had been grubbed. A comparison of available definitions of phenological stages in cherry previously used independently throughout Europe showed overlaps and shortcomings; hence, harmonisation was reached in this respect in the COST Cherry FA 1104 working group 2 (cherry phenology and climate change) based largely on the acceptance of the BBCH scale. This contribution presents the agreed phenology stages in both visual and wording evidence. Similarly, this contribution presents the agreed cultivars to be monitored in future for phenology and climate change effects for harmonisation. For sweet cherry, this EU-wide harmonisation includes 'Burlat', 'Cristobalina' and 'Rita' as early, 'Stella' and 'Van' as medium flowering and 'Sweetheart', 'Regina' and 'Bigarreau Noire de Meched/Germersdorfer' for late flowering cultivars for climate change effects. For sour cherry, this harmonisation resulted in 'Meteor korai' and 'Anglaise Hative' for early flowering, 'Chrisana Pandy' and 'Erdibotermo' for medium flowering and 'Schattemorelle', 'Iiva, Ujfehrtoifurtos (Balaton)' for late flowering.

Building climate resilient deciduous tree crops by deciphering winter dormancyBuds of deciduous tree crops enter winter dormancy in response to shorter photoperiods and lower temperatures in the fall. Winter dormancy comprises successive phases of endodormancy and ecodormancy. The transition from endodormancy to ecodormancy requires the exposure of dormant buds to a certain amount of chilling temperatures, whereas heat accumulation in ecodormant buds is essential for the successful shift from dormancy to active growth in tree crops (Lang et al., 1987). While bud dormancy allows plants to withstand harsh winters, timely bud break ensures their successful regrowth and production. As such, the initiation, progression, completion, and regulation of bud winter dormancy and break have been widely recognized for their importance in the survival and productivity of tree crops. However, climate change, often associated with warmer winters and temperature fluctuations (Inouye, 2022; Grossman, 2023), poses significant challenges to these processes, as alterations in temperature patterns can disrupt the delicate balance in temperature necessary for optimal bud dormancy and break.This Research Topic centers on the biochemical, genetic, physiological, and environmental regulation of bud winter dormancy and its break in various woody perennials, with a focus on the impact of climate change. It also explores breeding strategies to adapt to climate change, particularly rising winter temperatures. The eight articles encompass studies conducted on three continents, covering a range of crops including nut, fruit, ornamental, and beverage crops. They are briefly highlighted below.Gabay and Flaishman reviewed recent advancements in genetic and genomic resources as well as roles of genes, phytohormones, and metabolites related to dormancy regulation in pear (Pyrus spp.). They discussed the need for developing new pear cultivars with low chilling requirements and the challenges in pear breeding due to extended juvenility. They further emphasized the importance of understanding the genetic and physiological factors controlling bud dormancy in pear breeding. To this end, they pointed out the utility of quantitative trait loci (QTLs) in understanding dormancy regulation and developing genetic markers for marker-assisted selection in breeding. Lastly, the authors suggested Mediterranean climates could be used to simulate future temperate region climates for pear breeding.