Academic literature on the topic 'Budburst'

Ponderosa pine (Pinus ponderosa Lawson & C. Lawson var. scopulorum Engelm.) forests of the southwestern US are threatened by climate change and deforestation. Information about geographic patterns of provenance variation in budburst phenology is needed to make decisions about selecting seed sources for future planting. In this study, provenance variation in the budburst phenology of ponderosa pine seedlings was examined using common garden studies. Seedlings from 21 provenances, representing an elevational gradient in Arizona and New Mexico, were planted in July 2018 at a ponderosa pine-dominated field site in northern Arizona. Field budburst was monitored weekly on all seedlings in the spring of 2019. Field budburst was compared with budburst timing of the same provenances measured under greenhouse conditions. The hypotheses for this study were that (1) budburst varies among provenances, with earlier budburst in low-elevation provenances, and (2) differences in budburst timing among provenances are consistent for seedlings grown in greenhouse and field environments. Field results show that provenances vary in budburst date and that low- and middle-elevation provenances break bud sooner than high-elevation provenances. Field budburst date had a moderate, positive correlation with provenance mean annual precipitation (r = 0.522) and a moderate, negative trend with latitude (r = −0.413). Budburst date of provenances in the greenhouse had a moderate, positive trend with budburst date in the field (r = 0.554), suggesting application of greenhouse results to field plantings. Such information about provenance variation and environmental and geographic trends in budburst timing will be useful for developing species-specific seed transfer guidelines and effective assisted migration strategies in a changing climate.

The relationship between budburst phenology and damage by the pear thrips (Taeniothripsinconsequens (Uzel) (Thysanoptera: Thripidae)) to sugar maple (Acersaccharum Marsh.) foliage was investigated in two studies. In the first study, seedlings in cages were exposed to adult thrips at different stages of budburst. Compared with uninfested control seedlings, introduction of five adult thrips per bud reduced total leaf area and average leaf size, and caused chlorosis, tattering, and cupping of leaves. Leaf area reduction and damage symptoms were greater for seedlings exposed to thrips when leaf margins were first visible at the tip of the bud compared with earlier and later stages of budburst. In the second study, budburst date and number of thrips oviposition sites on leaves (an index of thrips activity) were measured in a common-garden test of maple saplings from open-pollinated families. Thrips activity was greater on early-breaking than late-breaking buds. Date of opening for these early-breaking buds coincided closely with peak capture of flying thrips. Both budburst date and number of oviposition sites on leaves differed among families. Sugar maple genotypes with late budburst escaped heavy thrips damage. The results indicate that timing of vegetative budburst in sugar maple can influence the degree of thrips damage.

The ecological impact of night-time lighting is of concern because of its well-demonstrated effects on animal behaviour. However, the potential of light pollution to change plant phenology and its corresponding knock-on effects on associated herbivores are less clear. Here, we test if artificial lighting can advance the timing of budburst in trees. We took a UK-wide 13 year dataset of spatially referenced budburst data from four deciduous tree species and matched it with both satellite imagery of night-time lighting and average spring temperature. We find that budburst occurs up to 7.5 days earlier in brighter areas, with the relationship being more pronounced for later-budding species. Excluding large urban areas from the analysis showed an even more pronounced advance of budburst, confirming that the urban ‘heat-island’ effect is not the sole cause of earlier urban budburst. Similarly, the advance in budburst across all sites is too large to be explained by increases in temperature alone. This dramatic advance of budburst illustrates the need for further experimental investigation into the impact of artificial night-time lighting on plant phenology and subsequent species interactions. As light pollution is a growing global phenomenon, the findings of this study are likely to be applicable to a wide range of species interactions across the world.

Background Experiencing an adequate amount of cold temperatures over winter is necessary for many temperate tree species to break dormancy and flower in spring. Thus, changes in winter and spring temperatures associated with climate change may influence when trees break dormancy and flower in the future. There have been several experimental studies that have quantified the effectiveness of cold temperatures for chilling requirements for vegetative budburst of temperate trees; however, there are few experimental studies addressing the chilling requirements for reproductive budburst of trees, as it is difficult to place reproductively mature trees in temperature-controlled environments. Methods To identify how changing temperatures associated with climate change may impact reproductive phenology, we completed a temperature-controlled growth chamber experiment using cuttings of reproductive branches of red alder (Alnus rubra), one of the most widespread hardwood tree species of the Pacific Northwest, USA. The purpose of this study was to examine how colder (4 °C) and warmer (9 °C) winter temperature regimes influenced the timing of reproductive budburst of red alder cuttings in spring. We also compared the date of budburst of cuttings to that of branches from intact trees. Results We found that cuttings flowered earlier after pretreatment with a 4 °C winter temperature regime than after a 9 °C winter temperature regime. We found no significant differences between the timing of male budburst of cuttings exposed to ambient conditions compared to male budburst of branches from intact trees. We used our experimental data to estimate a “possibility-line” that shows the accumulated chilling and forcing temperatures necessary prior to reproductive budburst of red alder. Discussion This study provides a preliminary indication that warmer winters with climate change may not be as effective as colder winters for satisfying chilling temperature requirements of a Northwest hardwood tree species.

Models to predict budburst and other phenological events in plants are needed to forecast how climate change may impact ecosystems and for the development of mitigation strategies. Differences among genotypes are important to predicting phenological events in species that show strong clinal variation in adaptive traits. We present a model that incorporates the effects of temperature and differences among genotypes to predict the timing of budburst of coast Douglas-fir (Pseudotsuga menziesii var. menziesii (Mirb.) Franco). The main components of the model are (i) functions to calculate the accumulation of chilling units (CU) and forcing units (FU) during dormancy and (ii) a function defining the combinations of CU and FU needed for budburst (the possibility line). The possibility line was fit to data from 59 populations subjected to eight different winter environments. Differences among populations were incorporated into the possibility line using population coefficients that vary the FU required for budburst. Correlations among the population coefficients and variables describing local environments supported the hypothesis that genetic variation in budburst is largely an adaptation to summer drought. The new model can be used to test potential seed transfers as a strategy to mitigate some of the effects of climate change.

<p style="text-align: justify;">The respective influences of the bud and leaves on stimulation of acrotony phenomenon was studied. Defoliation (all leaves at the stage budbursted + 30 days) and various bud ablation were made : buds 9, 10 ; 7, 8, 9, 10 ; 5, 6, 7, 8, 9, 10 ; 3, 4, 5, 6, 7, 8, 9, 10.</p><p style="text-align: justify;">Concerning the phenomen of acrotony, the role of apical bud and leaves developped on at 10 and 30 days after budburst were determined.</p><p style="text-align: justify;">The effect produced by excision of the apical buds shows that the two subadjacent buds were developped. All decapitation did not increase the percentage of budbreak.</p><p style="text-align: justify;">In all decapitations, the subadjacent buds were developped however, buds below were inhibed. The effect produced by excision of leaves in the second stage of development did not promote budbreak.</p><p style="text-align: justify;">On 10 bud canes, auxins synthesized in the developing young leaves seem to exercise their inhibiting effect on the budbreak of the subjacent buds.</p><p style="text-align: justify;">Cytokinins managed by the means of our operatory mode seem to reach the subjacents buds, modify the expression of the ramification of the canes with regard to the system usual acrotony and limit the inhibition basipetally. The budburst of the canes at a temperature of 18°C seems to be more important than that at 30°C day/ 20°night. Thus, the acrotony phenomenon decreases. When the apical branches are in second phase of growth, the size of the leaves become large. It seems that the leaves would exercise their inhibitions on the subjacent buds by the slant of the synthesized gibberillins and auxins. Cytokinins have no further role to play during this phase of growth and do not thwart anymore the inhibition. In the vineyard, the ANA treatment is totally inhibiting at 20 and 50 mg/l doses. In contrast, the 6BAP treatment at 20 mg/l shortly before budburst increases the budburst percentage for Muscatel of Italy.</p><p style="text-align: justify;">When the last treatment is performed during 25 days followed by a cytokinin treatment we notice budburst. The mechanism of these different growth regulators on the acrotony phenomenon has been discussed .</p>

Spraying of dormancy-breaking chemicals is a mandatory procedure to produce temperate fruits in low-chill regions. Although hydrogen cyanamide (HC) + mineral oil (MO) show efficiency enhancing budburst, the usage of HC is restricted in some countries due to its toxicity. Therefore, this research aimed to evaluate the efficiency of spraying different dormancy-breaking agents on ‘Eva’ apple tree buds, under the conditions of the Depressão Central of Rio Grande do Sul, Brazil. Different doses of Erger® (0, 2, 3, 4, 5%) + 3% Ca(NO3)2 were tested and compared with MO (4%) or MO (4%) + HC (0.6%). Budburst rate of apical and axillary buds, physiological alterations in buds, return bloom, yield and fruit weight were evaluated. Erger® treatments efficiently enhanced budburst, with a result equivalent to HC + MO treatment. The budburst rate increased as the Erger® dose increased, also causing the increment of the return bloom in the following year. However, doses of 4 and 5% caused the death of shoots. The activity of the peroxidases and the content of H2O2 in the buds were affected by the treatments. Yield and fruit mass were different in response to treatments, although the effect varied between years. Erger® + Ca(NO3)2 spraying increase budburst in apical and axillary buds of ‘Eva’ apple tree in low-chill conditions and doses up to 3% of the commercial product do not cause toxicity.

In order to produce the physiological bases for choosing early- flowering varieties that may avoid the depleted low winter temperatures, the early and late- opining apple variety Barkhar, Local and Strakhan (Malus sylvestris) were wont to study the relation between the seasonal changes and these balance of endogenous hormones and flower opining date. An improved understanding of the factors governing budburst and development, and their underlying mechanisms is crucial for management of trees performance and yielding. This study investigated variations in chilling requirements, bud burst and development in early and late varieties of apple trees. The budburst and hormonal profile of flower and vegetative buds of early and late varieties were additionally investigated. Results showed less bud burst in late varieties than in early ones. In the former, there were increased in promoters (indole-3-acetic acid and gibberellins) at budburst. Although endogenous inhibitors levels of abscisic acid were considerably reduced by bud development in all varieties. We conclude that late varieties (Strakhan) are less economical in manufacturing new growth, as indicated by less bud vigor at budburst than early varieties (Barkhar and local) and show a marked differential hormonal pattern throughout bud development compared to early varieties.

ABSTRACT Fluctuations in winter chilling availability impact bud dormancy and budburst. The objective of this work was to determine chilling requirements to induce and overcome endodormancy (dormancy controlled by chilling) of buds in different grape cultivars. ‘Chardonnay’, ‘Merlot’ and ‘Cabernet Sauvignon’ shoots were collected in Veranópolis-RS vineyards in 2010, and submitted to a constant 3 °C temperature or daily cycles of 3/15 °C for 12/12h or 18/6h, until reaching 1120 chilling hours (CH, sum of hours with temperature ≤ 7.2 °C). Periodically, part of the samples in each treatment was transferred to 25 °C for budburst evaluation (green tip). Chilling requirements to induce and overcome endodormancy vary among cultivars, reaching a total of 136 CH for ‘Chardonnay’, 298 CH for ‘Merlot’ and 392 CH for ‘Cabernet Sauvignon’. Of these, approximately 39, 53 and 91 CH are required for induction of endodormancy in the three cultivars, respectively. The thermal regimes tested (constant or alternating) do not influence the response pattern of each cultivar to cold, with 15 °C being inert in the CH accumulation process. In addition, time required to start budburst reduces with the increase in CH, at a rate of one day per 62 CH, without significant impacts on budburst uniformity.

Delaying winter pruning until after budburst is a technique that can retard vine phenological phases and reduce grape sugar concentration at harvest. Given these characteristics, many studies have recently been conducted to verify the ability of pruning after budburst to contrast the negative effects of climate change. In our trial, vines of the cv. Merlot, trained to a VSP spur pruned cordon, were pre-pruned leaving 8 nodes per shoot and hand finished when the shoots sprouted by the apical nodes were at BBCH13 (treatment LP) and BBCH18 stage (treatment VLP). Vines refinished during winter were used as control (WP). Anthocyanins and tannins of skin and seeds were analysed after both exhaustive extraction (total content) and extraction conducted with a hydroalcoholic solution (extractable portion). Vines refinished after budburst showed reduced leaf area, yield, cluster and berry weights; technological maturity of these vines was delayed as lower sugar concentration and pH were observed at harvest. Treatment VLP had a stronger effect than LP on these parameters. Considering phenolic compounds, the skin and seed tannin concentration increased only in VLP, while no effect was found on anthocyanins. In conclusion, delaying pruning until after budburst revealed interesting prospects for contrasting the negative effects of climate change.

Both the physiological and biochemical control of budburst in the grapevine, Vitis Vinifera L. were investigated. It was found that the accuracy of a predictive model for grapevine budburst based on ambient temperature was limited under the experimental conditions. There was a significant correlation of 4.7 ± 0.3 days between the days of maximal xylem exudation and budburst over the 3 years of investigation. The co-relationships between daily xylem exudate volume and a range of environmental parameters were considered. It was found that soil temperature was highly correlated against daily xylem exudation. Ambient temperature and soil moisture were significantly correlated with xylem exudation, however the coefficients of correlation were much lower than that of soil temperature. Rainfall showed only a very limited correlation with daily xylem exudate flow. Seasonal variations in the pH and the carbohydrate and inorganic nutrient concentrations of xylem exudate were investigated. Exudate carbohydrate concentrations fell from 660 µM before the day of maximal xylem exudation to zero levels within 4 weeks. Xylem exudate pH was found to consistently fall to a minimum at the time of maximal exudate flow. Exudate concentrations of the metallic cofactors Ca, K, Mg, Mn and Zn varied directly with daily exudate flow, suggesting some sort of flow-dependent mobilisation of these nutrients. A growth promontory oligosaccharide fraction was prepared by partial acid hydrolysis of grapevine primary cell wall material. This fraction significantly increased control growth of the Lemna minor L. bioassay over a limited ‘window’ of bioactivity. A growth inhibitory oligosaccharide fraction, similar in activity to abscisic acid was isolated from grapevine xylem exudate prior to budburst. The exudate concentration or efficacy of this substance declined after budburst such that there was no apparent growth inhibition. A model is proposed for grapevine budburst whereby an oligosaccharide growth inhibitor is gradually removed from the xylematic stream under the effects of soil temperature, allowing the surge of metabolic activity and vegetative growth that constitute budburst.

Over the last 150 years the natural nighttime environment has been drastically altered by the proliferation of artificial light. The amount of artificial light at night is on the increase, and there is a current trend to replace older lighting with more energy efficient types such as light emitting diodes (LEDs) or ceramic metal halide; in Cornwall, UK, there has been a relatively recent replacement of the street lighting, from low pressure sodium to ceramic metal halide. Alongside the increasing amount of artificial nighttime light, recent research has highlighted declines in macro moth numbers. Given the well-known ‘flight-to-light’ behaviour of moths, and the negative effects this behaviour can have, alongside other known and potential ways in which nighttime light can affect moths, the increasing amount of artificial light in the environment is a suspected contributor to the declines. It is particularly important to understand how modern lighting technologies will impact upon moths, as different spectra of light are known to vary in terms of how attractive they are. As a means to determine the potential impact of different street lighting types on moths, particularly the ceramic metal halide lighting rolled out in Cornwall, UK, we compared the attractiveness to macro moths, of a number of increasingly used, energy efficient, street lighting types. We found that shorter wavelength metal halide lighting attracted significantly more individuals and species of moth than longer wavelength high pressure sodium lighting. In a second experiment, we also found ceramic metal halide lighting to be more attractive to macro moths than LED lighting. Reduced emissions of short wavelength UV light was deemed the likely reason behind the fewer macro moths attracted to the high pressure sodium and LED lighting. Interestingly, we also found striking differences in the relative attractiveness of the different lighting types to different moth groups. The metal halide lighting attracted significantly more Noctuidae than high pressure sodium lighting, whereas both high pressure sodium and metal halide lighting were equally attractive to Geometridae. Understanding accurately the extent to which different groups of moth are attracted to different wavelengths of light could be useful in determining the impact of artificial light on moth populations. In addition to impacting moths through attraction, artificial light has the potential to alter the day length as perceived by organisms, which at mid- to high latitudes is utilised by certain species as an abiotic cue to ensure the coincidence of development with favourable environmental conditions. Due to a paucity of knowledge on how raised ambient nighttime light levels affect moths and the trophic levels with which they interact, we carried out analyses into the impact of nighttime light on the winter moth and its host plant oak; a well-studied model system, where synchrony between moth egg hatch and oak budburst is important for the moth’s survival. Firstly we carried out an analysis looking at the relationship between the amount of nighttime light and the date of oak budburst. Spatially referenced budburst dates were matched with satellite imagery of nighttime lighting and average spring temperature data, and the relationship between the variables was analysed. Model predictions suggested that oak budburst occurs earlier in brighter areas. In addition, the predicted advance of budburst in brighter areas was still apparent when analysing only the data points that fell outside of large urban areas, where the urban heat island effect is likely reduced. The findings suggested that artificial nighttime light may be causing an advance in oak budburst. To follow up the spatial analysis we carried out a field experiment. We used light cages that simulated various nighttime lighting scenarios to test whether oak budburst and winter moth egg hatch were affected by low intensity light at night. In contrast to the spatial analysis, there was no significant relationship found between light treatment and the phenology of either oak budburst or winter moth egg hatch. However, there was a suggestion in the data that the higher buds of the oak saplings emerged earlier in the yellow light treatment, highlighting the need for further research into the potential impact of artificial nighttime light on phenology and species interactions. In conclusion, the findings of this research project provide information useful to those seeking ecologically sensitive lighting solutions, and also highlight a potential tool to assist in determining whether light at night is a causative factor behind apparent moth declines. In addition, they suggest that artificial light at night may be affecting the phenology of an ecological system at a national scale. Finally, this research project has highlighted the complexity of the ecological impacts of artificial light at night, and also a need for further research.

This thesis contains information from the study of Norway spruce clones, which possess certain inheritable traits (1) of value for timber used in building constructions (i.e. higher wood basic density, elasticity, and resistance to crashing) and (2) greater wood yield. The following growth and quality traits of 90 clones in Baisogala seed orchard of Radviliškio forest enterprise were assessed: stem height and diameter, crown diameter, branching type and class of budburst. Significance of differences among the clones was estimated for all the these traits. Correlation coefficients among qualitative and quantitative traits were calculated. Owing to relatively lower radial increment and thicker annual ring, clones of brushy and flat branching types produced wood of a higher basic density and, thus, of a greater quality. A more slowly growth of clones with the above mentioned branching types was observed on their progeny as well. Therefore, if there is no need for stems of a relatively larger diameter, it would be more rational to produce Norway spruce stands of flat and brushy branching types.

La phénologie du débourrement est un caractère majeur d’adaptation des arbres à leurenvironnement en milieu tempéré. Notre objectif a été de caractériser les contraintes biotiques (oïdium) etabiotiques (températures hivernales et printanières / gels tardifs) s’exerçant sur le débourrement afind’expliquer les patrons de variation phénologique intra et inter populationnelle observés chez le chêne(Quercus petraea) le long d’un gradient altitudinal. Nous avons utilisé une approche combinantobservations in situ, expérimentation, et modélisation. Nous avons mis en évidence que l’évitement desgels tardifs printaniers est un caractère adaptatif majeur le long du gradient altitudinal. La tardiveté dudébourrement pourrait être due à des besoins plus importants en température de forcing. Par ailleurs, lechampignon n’est pas adapté localement à la phénologie de son hôte et les individus et les populationssont alors inégalement exposés à la maladie. En montant en altitude, les chênes sont de plus en plusexposés au champignon, mais les facteurs environnementaux sont défavorables à une plus forte infection.A basse altitude, l’oïdium et les gels tardifs favorisent des phénotypes phénologiques opposés(respectivement précoces vs. tardifs) ; la combinaison des deux contraintes pourrait donc contribuer aumaintien de la forte diversité phénologique observée. D’autre part, nous avons observé que l’infection parl’oïdium engendre une augmentation du polycyclisme chez les semis de chêne au cours de la saison decroissance, ce qui les rend moins résistants aux gels hivernaux. Nous montrons qu’il est important que lesmodèles phénologiques à visée prédictive intègrent la phase de chilling aboutissant à la levée dedormance. Le manque de chilling ne semble pas encore un facteur limitant, mais la tendance actuelle à undébourrement de plus en plus précoce sera probablement freinée voire inversée au milieu du siècle enbasse altitude, dans la marge sud de distribution de Q. petraea
Budburst phenology is a major adaptive trait of trees to the environment in temperateclimate. Our aim was to characterize the biotic (powdery mildew) and abiotic (winter and springtemperatures / spring frost) constraints acting on budburst in view to explain the patterns of intra and interpopulations’ phenological variation observed in sessile oak (Quercus petraea) along an elevation gradient.We based our approach on in situ monitoring, experimentation and modeling. Our results highlight that theavoidance of late spring frosts is a major adaptive trait along the elevation gradient. The lateness inbudburst might be due to higher requirements in forcing temperatures. Otherwise, the fungus is not locallyadapted to its host phenology so oak individuals and populations are unequally exposed to the disease.With increasing elevation, oaks are more and more exposed to the fungus, but the environmental factorsare unfavorable to higher infection. At low elevation, powdery mildew and late spring frosts favor oppositephonological phenotypes (early-flushing vs. late-flushing trees, respectively); the combination of the twopressures may thus contribute to the maintenance of the observed high phenological diversity. We alsoshowed that powdery mildew infection induced an increased polycyclism during the growing season in oakseedlings, which made them less resistant to winter frosts. Predictive phenological models will have toinclude the chilling phase which conditions dormancy breaking. Although the lack of chilling is not yet alimiting factor, the current trend in increasingly advanced budburst will certainly be slowed or even reversedin the middle of the century at low elevation, in the southern margin of the distribution area of Q. petraea

Le pommier (Malus Xdomestica Borkh.) cultivé en climat à hiver doux, avec un manque d'une quantité suffisante d'heures de températures froides, présente des anomalies morphologiques et physiologiques. Sur le plan de la phénologie, il s'agit notamment d'un débourrement printanier tardif et désynchronisé entre les différents bourgeons d'un même arbre. Sur le plan agronomique, la floraison et la nouaison sont irrégulières et étalées dans le temps et conduisent à une faible production de fruits. L'objectif de ce travail de thèse est premièrement de mieux caractériser les effets des températures hivernales sur le débourrement et la croissance des bourgeons axillaires en distinguant les effets respectifs des températures hivernales et du génotype. Il s'agit ensuite de vérifier l'hypothèse que les effets des températures sur le débourrement du bourgeon s'effectue via les effets sur son statut hydrique. Les travaux ont été réalisés en France et au Brésil. En France, les expérimentations ont porté sur quatre cultivars à fort besoin (‘Granny Smith', ‘Royal Gala', ‘Starkrimson') ou faible besoin (‘Condessa') en froid, cultivés en hiver froid (conditions extérieures) et doux (serres climatisées). Nous montrons que le débourrement résulte d'une séquence d'évènements où la température hivernale joue un rôle primordial sur les mécanismes de sortie de dormance et donc sur le débourrement proprement dit, durant la période froide. Les caractéristiques propres du cultivar jouent par contre un rôle dans la croissance ultérieure des bourgeons et donc dans l'architecture finale de la pousse du pommier. Par ailleurs, la chute tardive des feuilles, caractéristique du pommier en hiver doux, a peu d'effets sur le débourrement et la croissance des bourgeons. L'analyse du statut hydrique des bourgeons a été réalisée sur le tiers distal des pousses de pommier caractérisé par une forte fréquence de ramification en climat à hiver froid. Nous montrons que, dans la période allant de l'endordormance à la phase de pré-débourrement, la conductance hydraulique à la jonction entre l'axe porteur et le bourgeon varie peu au cours de l'hiver et entre cultivars. Par ailleurs, durant cette même période le potentiel hydrique intra-bourgeon reste négatif, entre -4.35 and -2.24 MPa. Enfin, quel que soit le cultivar, nous ne montrons pas de relation entre les températures hivernales, le potentiel hydrique ou la teneur relative en eau des bourgeons, et l'aptitude au débourrement ultérieur. Ces résultats suggèrent que le bourgeon est hydrauliquement isolé de son axe porteur pendant toute la période hivernale jusqu'à quelques jours précédant le débourrement. Les expérimentations au Brésil ont porté sur le cultivar ‘Eva ‘ à faible besoin en froid, cultivés en conditions naturelles d'hiver doux. Il s'agissait de vérifier les effets possibles de la position du bourgeon le long de l'axe porteur sur sa taille et sa teneur relative en eau. Nous montrons que, tout au long de l'hiver, les bourgeons distaux sont caractérisés par une plus grande taille et une teneur relative en eau plus élevée que les bourgeons proximaux avec une forte augmentation de la teneur relative en eau une semaine avant le débourrement printanier. Le débourrement acrotone semble donc résulter d'une évolution rapide du statut hydrique du bourgeon en fin d'écodormance. L'ensemble des résultats acquis en France et au Brésil, sur des cultivars caractérisés par des besoins variables en froid hivernal, indique que l'aptitude au débourrement printanier des bourgeons de pommier est davantage lié à un « effet rameau entier » qu'au statut hydrique proprement dit des bourgeons individuels, tout au moins jusqu'à quelques jours avant le débourrement effectif. La pousse annuelle de pommier apparait donc comme une unité morphologique et physiologique intégrée qui, dans un contexte climatique donné, conditionne le statut hydrique de chaque bourgeon et son aptitude au débourrement
The apple tree (Malus Xdomestica Borkh.) presents morphological and physiological anomalies when grown in mild winter climates with insufficient winter chilling to overcome winter dormancy. Symptoms are typically delayed and erratic budburst, entailing desynchronized flowering and fruit-set and poor agronomic performances. This thesis aimed at gaining more insights on the following issues. Firstly, what are the effects of winter temperatures on axillary burdburst and bud outgrowth, and what are the respective effects of winter temperatures and cultivar?, and secondly, is there a link between the temperature-dependent budburst and bud water status? Works were done in France and Brazil. In France, experiments were carried out in controlled conditions on four apple cultivars characterized by either high chilling (‘Granny Smith', ‘Royal Gala', ‘Starkrimson') or low chilling (‘Condessa') requirements and were submitted to outdoor-cold and greenhouse-mild winter temperatures. We showed that the actual shoot architecture and budburst resulted from an ordered sequence of events with a pivotal role of winter temperatures on the dormancy completion of individual lateral buds. Endogenous factors related to the cultivar branching pattern overtook the temperature effect on the lateral bud outgrowth. Furthermore, the delayed senescence and subsequent leaf persistence during winter, characterizing the apple tree in the mild winter temperature conditions, had only a weak effect on the topological distribution of budburst and lateral outgrowth. The analyses of bud water status were done on distal buds only, characterized by high budburst frequency in cold winter conditions. We showed that, from endodormancy to the pre-budburst stage, xylem conductance at the stem-to-bud junction did not show consistent changes across cultivars and winter temperature treatments. Bud water potential had negative values, between -4.35 and -2.24 MPa, depending on cultivars and winter temperature treatments. Moreover, whatever the cultivar, there were no significant trends across dates for the effects of winter temperatures on bud water potential and relative water content without a consistent relationship with actual spring budburst frequency. These results suggested that lateral buds were hydraulically isolated from the parent stem during winter until a few days before budburst. The other set of experiments was carried out in Brazil, under mild winter conditions, on the low chilling apple cultivar ‘Eva'. The objectives were to gain more insights on the effect of the position of the over-wintering lateral bud along the whole-parent shoot on bud size and water content. Results highlighted that distal buds were larger and had a higher water content than proximal buds with a strong increase of water content a week before spring budburst. It was concluded that the acrotonic pattern of budburst was mainly established during ecodormancy. As a whole, we showed that spring budburst seemed more related to a whole-shoot effect than to the water status of the individual bud during winter dormancy. Our study substantiated the importance of the whole shoot as an integrated morphological and physiological unit in driving budburst and further growth

Submitted by Gabriela Lopes (gmachadolopesufpel@gmail.com) on 2016-09-14T18:22:14Z No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Tese Juliano Dutra Schmitz.pdf: 9582623 bytes, checksum: f579b0458e2ab6f4ae5579715de842ea (MD5)
Approved for entry into archive by Aline Batista (alinehb.ufpel@gmail.com) on 2016-09-15T19:46:43Z (GMT) No. of bitstreams: 2 Tese Juliano Dutra Schmitz.pdf: 9582623 bytes, checksum: f579b0458e2ab6f4ae5579715de842ea (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)
Made available in DSpace on 2016-09-15T19:46:43Z (GMT). No. of bitstreams: 2 Tese Juliano Dutra Schmitz.pdf: 9582623 bytes, checksum: f579b0458e2ab6f4ae5579715de842ea (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Previous issue date: 2014-12-03
Conselho Nacional de Pesquisa e Desenvolvimento Científico e Tecnológico - CNPq
A macieira (Malus X domestica Borkh.) apresenta anomalias fisiológicas quando cultivada em regiões de inverno ameno, onde o frio hibernal é insuficiente para superação da dormência. Assim, na presente tese foram estudados três temas de pesquisa. No tema 1 estudou-se a distribuição e fenologia da brotação e crescimento inicial da ramificação primaveril; No tema 2 estudou-se a brotação primaveril através da determinação do status hídrico de gemas laterais e da condutância hidráulica do xilema. O tema 3 realizou-se a análise do comportamento da brotação primaveril de uma cultivar de baixo exigência em frio cultivada em inverno ameno. Para isso, foram montados dois dispositivos experimentais: Experimento 1: realizado em Montpellier/França, onde foram estudadas quatro cultivares de macieira, com diferentes requerimentos em frio (‘Condessa’, ‘Granny Smith’, ‘Royal Gala’ e ‘Starkrimson’), submetidas a dois regimes térmicos (inverno frio, condições naturais de Montpellier; e inverno ameno, temperatura controlada em casa-de-vegetação). Experimento 2: realizado com a cultivar de baixo requerimento em frio ‘Eva’ sob regime térmico hibernal ameno (condição natural de Capão do leão/Brasil). A partir do experimento 1, dois artigos foram redigidos . Conclui-se a partir dos resultados obtidos (artigos 1 e 2) que as temperaturas hibernais têm o principal efeito na distribuição da ramificação ao longo do eixo principal e no tempo para brotação; a presença de folha das plantas submetidas ao regime térmico de inverno ameno não afeta a distribu ição de ramos prolépticos vegetativos; a cultivar exerce efeito no crescimento da ramificação. Com relação ao status hídrico, conclui-se que durante o inverno (período de dormência) as gemas laterais permanecem hidraulicamente isoladas do eixo principal; assim como o potencial de brotação está relacionado a um efeito ramo inteiro (todo eixo principal) do que ao potencial individual de cada gema lateral. Através do experimento 2, um artigo foi elaborado, tendo por objetivo testar a hipótese que a posição em que a gema lateral está localizada sobre o eixo principal têm efeito na brotação primaveril, no conteúdo de água e tamanho das mesmas. Pode-se concluir deste estudo que uma semana antes a brotação, as gemas localizadas na zona distal possuem maior potencial de crescimento (maior frequência de brotação e menor tempo médio para brotação), além de apresentarem maior umidade ponderal e tamanho.
The apple tree (Malus X domestica Borkh.) presents morphological and physiological anomalies when grown in mild winter climates with insufficient winter chilling to overcome winter dormancy. Symptoms are typically delayed and erratic budburst, entailing desynchronized flowering and fruitset and poor agronomic performances. This thesis aimed at gaining more insights on the following issues. Firstly, what are the effects of winter temperatures on axillary burdburst and bud outgrowth, and what are the respective effects of winter temperatures and cultivar?, and secondly, is there a link between the temperature-dependent budburst and bud water status? Works were done in France and Brazil. In France, experiments were carried out in controlled conditions on four apple cultivars characterized by either high chilling (‘Granny Smith’, ‘Royal Gala’, ‘Starkrimson’) or low chilling (‘Condessa’) requirements and were submitted to outdoor-cold and greenhouse-mild winter temperatures. We showed that the actual shoot architecture and budburst resulted from an ordered sequence of events with a pivotal role of winter temperatures on the dormancy completion of individual lateral buds. Endogenous factors related to the cultivar branching pattern overtook the temperature effect on the lateral bud outgrowth. Furthermore, the delayed senescence and subsequent leaf persistence during winter, characterizing the apple tree in the mild winter temperature conditions, had only a weak effect on the topological distribution of budburst and lateral outgrowth. The analyses of bud water status were done on distal buds only, characterized by high budburst frequency in cold winter conditions. We showed that, from endodormancy to the pre-budburst stage, xylem conductance at the stem-to-bud junction did not show consistent changes across cultivars and winter temperature treatments. Bud water potential had negative values, between -4.35 and -2.24 MPa, depending on cultivars and winter temperature treatments. Moreover, whatever the cultivar, there were no significant trends across dates for the effects of winter temperatures on bud water potential and relative water content without a consistent relationship with actual spring budburst frequency. These results suggested that lateral buds were hydraulically isolated from the parent stem during winter until a few days before budburst. The other set of experiments was carried out in Brazil, under mild winter conditions, on the low chilling apple cultivar ‘Eva’. The objectives were to gain more insights on the effect of the position of the over-wintering lateral bud along the whole-parent shoot on bud size and water content. Results highlighted that distal buds were larger and had a higher water content than proximal buds with a strong increase of water content a week before spring budburst. It was concluded that the acrotonic pattern of budburst was mainly established during ecodormancy. As a whole, we showed that spring budburst seemed more related to a whole-shoot effect than to the water status of the individual bud during winter dormancy. Our study substantiated the importance of the whole shoot as an integrated morphological and physiological unit in driving budburst and further growth.

Recent changes in the timing of annual events are a sign that climate change is already impacting ecosystems. Carbon sequestration by forests increases with longer growing seasons. Biodiversity can be affected by mis-timing of events through shading interactions and frost damage. Projecting forests' ability to provide these ecosystem services in the future requires an understanding of trees' phenological responses to a new climate. I begin by proposing a first order definition of an `optimal' phenological response to warming: that the mean temperature following budburst should remain essentially constant. Analogously, the temperature preceding senescence can serve the same role.

To understand which environmental cues will drive future changes in phenology, I assimilate clues from observational and experimental literature. For budburst in woody plants, spring warmth, over-winter chilling and light drive nearly all behavior, but species' responses vary widely. Species using chilling or light as safety mechanisms against budburst during mid-winter thaws are thought to be less able to phenologically track a warming climate. However, I show that even species cued solely by spring warmth are likely to under-track temperature changes. Fall cues are more idiosyncratic, and a plant's driver of senescence is likely to vary from year to year.

Models are a tempting method to untangle species budburst cues and forecast phenology under warmer climate scenarios. I tested two models' ability to recover parameters used to simulate budburst data. The simpler model was cued only by spring warmth while the complex one modulated warmth requirements with chilling exposure. For the simple model, parameters could be recovered consistently from some, but not all, regions of parameter space. The complex model's parameters were largely unrecoverable. To understand the consequences of parameter uncertainty, I applied both models to an 18 year phenological record of 13 deciduous tree species. While a few species fell into identifiable regions of the simple model's parameter space, most did not, and projected budburst dates had wide parameter-derived uncertainty intervals. These bands were wider still under a 5°C warming scenario. Even greater uncertainty resulted from the complex model.

To better understand plants' potential for growing season extension I subjected seedlings to warmer climates in a series of open-topped chambers in sites at each end of the eastern deciduous biome. Soil and air were heated to 3 or 5°C above ambient, or left unheated. For nearly all species, warming hastened budburst and germination and delayed senescence. However, these events failed to track temperature changes, happening at warmer temperatures in hotter chambers. Individual species showed a remarkable variability of all events' dates within treatments, and even within chambers. Because phenological traits are heritable, this offers a potential for evolutionary response to climate change.

This research has shown that while individual trees extend their growing seasons under warmer temperatures, they typically under-respond to the magnitude of warming, suggesting forests' capacity for increased carbon sequestration may reach a limit. However, within populations, trees vary substantially in their phenological responses, forming a possibility for evolutionarily adaptation to changing cues.

Dissertation