Carotenoid composition and down regulation of photosystem II in three conifer species during the winter

Seedlings and coppice shoots of Betula pubescens Ehrh. were grown under controlled conditions designed to simulate the annual growth cycle, and a water stress was introduced during the short day (SD). Alleviation of hud dormancy after increasing periods at chilling temperatures was tested under long day (LD) conditions. Abscisic acid (ABA) was analysed in leaf and bud samples by gas chromatography-mass spectrometry using [²H₄]ABA as the internal standard. Elongation growth of coppice shoots was faster than that of seedlings under both LD and SD conditions, while the final growth cessation occurred in a similar manner and was not affected by water stress, which significantly reduced growth rate in both plant types. Bud dormancy gradually decreased with increasing length of chilling, starting from the basal parts of the plant axis. Water stress did not retard hudhurst. but rather improved it in the chilled coppice shoots and in the non-chilled and partially chilled seedlings. Water content of buds was higher in coppice shoots than in seedlings, but after exposure to SD. it gradually decreased to 45% in both plant types and was not affected by water stress or chilling. The ABA level in both leaves and buds increased during SD treatment and was" enhanced by water stress. No clear differences in bud ABA level were found between the seedlings and coppice shoots under SD conditions, although coppice shoots had less ABA during the preceding LD conditions. There was, in general, no clear effect of chilling on bud ABA level. Budbursl in chilled, single-node cuttings was inhibited by external ABA treatment, which raised the internal ABA levels 10 to 150 times above normal. The observed correlation between ABA level and water content in buds during induction of dormancy under SD and water stress conditions indicates a possible role for ABA in the regulation of dormancy.     

Effects of constant and fluctuating temperature on time to budburst in Betula pubescens and its relation to bud respiration

 Effects of fluctuating and constant temperatures on budburst time, and respiration in winter buds were studied in Betula pubescens Ehrh. Dormant seedlings were chilled at 0°C for 4 months and then allowed to sprout in long days (LD, 24 h) at constant temperatures of 6, 9, 12, 15, 18 and 21°C, and at diurnally fluctuating temperatures (12/12 h, LD 24 h) with means of 9, 12, 15 and 18°C. No difference in thermal time requirements for budburst was found between plants receiving constant and fluctuating temperatures. The base temperature for thermal time accumulation was estimated to 1°C. Respiration in post-dormant (dormancy fully released) excised winter buds from an adult tree increased exponentially with temperature and was 20 times as high at 30°C than at 0°C. However, respiration in buds without scales was 30% higher at 0°C, and it was 2.7 times higher at 24°C than in intact buds. Thus, the tight bud scales probably constrain respiration and growth and are likely to delay budburst in spring. Arrhenius plots of the respiration data were biphasic with breaks at 13–15°C. However, this phase transition is unlikely to be associated with chilling sensitivity since the present species is hardy and adapted to a boreal climate. Received: 10 January 1997 / Accepted: 23 June 1997     

Daylength and thermal time responses of budburst during dormancy release in some northern deciduous trees

Dormancy release and thermal time to budburst as affected by duration of chilling outdoors, followed by different flushing temperatures and daylengths in a phytotron, were studied in cuttings of several northern tree species. In Betula pubescens, B. pendula and Prunus padus vegetative buds were released from dormancy already in December, in Populus tremula in January, whereas in Alnus incana and A. glutinosa dormancy was not released until February. Thermal time (day degrees >0°C) to budburst decreased non-linearily with increasing duration of chilling (i. e. duration outdoors), and the slope of this relationship differed among species. The estimated effective base temperature for accumulation of thermal time varied from + 1°C in P. tremula to −4°C in P. padus . The use of 0°C as base temperature is recommended. Long days reduced the thermal time to budburst at all flushing temperatures (9, 15 and 21°C) in all the above species and in Corylus avellana , whereas Sorbus aucuparia and Rubus idaeus showed no daylength response. Since the chilling requirement of all species was far exceeded even in a winter with January-March temperatures 6.5°C above normal, it is concluded that under Scandinavian conditions, the main effect of climatic warming would be earlier budburst and, associated with that, a longer growing season and increased risk of spring frost injury.     

Photoperiodic control of dormancy in Sedum telephium and some other herbaceous perennial plants

The environmental control of dormancy and flowering of the herbaceous perennial Sedum telephium was studied in controlled environments. Short photoperiods induced growth cessation and the formation of resting buds in both seedlings and mature plants, whereas long photoperiods resulted in immediate growth activation of dormant buds. No chilling was required for dormancy release, even in plants induced to dormancy and maintained at high temperature (21°C) for more than 3 months. The critical photoperiod for dormancy release was about 15 h, a minimum of four long-day (LD) cycles (24 h) being required. The true photoperiodic nature of this response was ascertained by night interruption experiments. Flowering of S. telephium was found to have an obligatory LD requirement, with no requirement for vernalization. The critical photoperiod and minimum number of inductive cycles for floral induction were the same as for dormancy release. Dormancy release by long days was also obtained in preliminary experiments with three other herbaceous perennials. The eco-physiological significance of photoperiodic control of dormancy is discussed, and it is concluded that the mechanism ensures stability of winter dormancy, even under conditions of climatic warming.     

Periodicity of response to abscisic acid in lateral buds of willow (Salix viminalis L.)

Aseptically cultured lateral buds of Salix viminalis L. collected from field-grown trees exhibited a clear periodicity in their ability to respond to exogenous abscisic acid (ABA). Buds were kept unopened by ABA only when the plants were dormant or entering dormancy. Short days alone did not induce bud dormancy in potted plants but ABA treatment following exposure to an 8-h photoperiod prevented bud opening although ABA treatment of buds from long-day plants did not. Naturally dormant buds taken from shoots of field-grown trees and cultured in the presence of ABA opened following a chilling treatment. In no cases were the induction and breaking of dormancy and response to ABA correlated with endogenous ABA levels in the buds.Abbreviations ABA abscisic acid - GA₃ gibberellic acid - HPLC high-performance liquid chromatography - LD long day - MeABA methyl ABA - PAR photosynthetically active radiation - SD short day     

Climatic determinants of budburst seasonality in four temperate-zone tree species

Several physiological processes controlling tree phenology remain poorly understood and in particular bud dormancy. Many studies have emphasised the action of chilling temperatures in breaking dormancy. However, the effect of the preceding summer temperatures has rarely been investigated although there is some evidence that they may be involved in the settlement and intensity of dormancy as well as cold acclimation. In this paper, thermal time to budburst in relation to the duration of chilling outdoors, preceding summer temperatures and forcing temperatures was studied by outdoors experiments in seedlings of Platanus acerifolia , Vitis vinifera , Quercus pubescens and Castanea sativa . Results showed that temperatures of the preceding summer had no significant effect on the timing of budburst, P. acerifolia and Q. pubescens showed a very weak response to the duration of chilling, and the phenological characteristics of each species were found to be adapted to the climate conditions of its own geographical area. The phenological model used in this study explained 82–100% of the variance of the data without taking into account summer temperatures. Thus, although summer temperatures may be well involved in the intensity of dormancy and cold hardiness, they do not significantly affect budburst and therefore may not need to be considered in phenological models for predicting budburst.     

Effects of low temperature on diapause termination and body colour change in adults of a stink bug, Plautia stali

Abstract. Diapause adults of Plautia stali Scott maintained at 20°C under short day conditions (LD 12:12 h) were exposed to four temperatures of 5–20°C to examine the effect on diapause development which was assessed in terms of oviposition. Diapause adults kept at 20°C under short day conditions changed their body colour gradually from brown to green and started egg laying after a prolonged preoviposition period. Those transferred to either 10 or 15°C also showed colour change but did not lay eggs. Bugs exposed to 5°C underwent neither body colour change nor oviposition and died more rapidly than those kept at higher temperatures. When 30-day-old diapause adults were chilled at 5, 10 or 15°C for 30 or 60 days and returned to 20°C and long day conditions (LD 16:8 h), the preoviposition period varied primarily depending on the chilling, but not on the temperature. On the other hand, when 60day-old diapause adults chilled for 30 days were observed at 20°C and long day conditions, their preoviposition period tended to be longer as the chilling temperature was lower In this case, a temperature of 10°C appeared to intensify diapause. Therefore, the effect of chilling on diapause development varied depending on the age at which insects were chilled. When chilled bugs were transferred to short day conditions at 20°C, most females failed to lay any eggs and some turned green, then after a while, some green bugs changed to brown again. These results indicate that bugs remained sensitive to short day conditions even after a 60-day chilling at 10 or 15°C.     

Are budburst dates,dormancy and cold acclimation in walnut trees (<Emphasis Type="Italic">Juglans regia</Emphasis> L.) under mainly genotypic or environmental control?

As observed for most stresses, tree frost resistance can be split into two main processes: avoidance and tolerance. Avoidance of freezing is achieved by introducing species only in the climatic context in which the probability of freezing events is very low for the sensitive stages of buds or stems; i.e., when good synchronism exists between the annual cycle and the critical climatic periods. Buds become able to grow only after chilling requirements have been satisfied (endodormancy released) during winter; they subsequently break after heat requirements have been completed (end of ecodormancy) in early spring. Actually, this period is often subject to more or less severe freezing events. Trees are also able to adjust their freezing tolerance by increasing their capacity of extracellular freezing and decreasing the possibility of intracellular freezing through the process of frost acclimation. Both freezing resistance processes (avoidance and tolerance) are environmentally driven (by photoperiod and temperature), but there are also genotypic effects among species or cultivars. Here, we evaluated the degree to which differences in dormancy release and frost acclimation were related to environmental and genetic influences by comparing trees growing in common garden conditions. This investigation was carried out for two winters in lowland and mountain locations on different walnut genotypes differing significantly for budburst dates. Chilling requirement for endodormancy release and heat requirement during ecodormancy were evaluated in all situations. In addition, frost acclimation was assessed by the electrolyte leakage method on stems from the same trees before leaf fall through budburst. No significant differences were observed in chilling requirements among genotypes. Moreover, frost acclimation dynamics were similar between genotypes or locations when expressed depending on chilling units accumulated since 15 September as a time basis instead of Julian day. The only exception was for maximal frost hardiness observed during winter with the timber-oriented being significantly more resistant than fruit-oriented genotypes. Heat requirement was significantly different among genotypes. Thus, growth was significantly faster in fruit-oriented than in wood-oriented genotypes. Furthermore, among wood-oriented genotypes, differences in growth rate were observed only at cold temperatures. Frost acclimation changes differed significantly between fruit- and wood- walnuts from January through budburst. In conclusion, from September through January, the acclimation dynamic was driven mainly by environmental factors whereas from January through budburst a significant genotype effect was identified in both frost tolerance and avoidance processes.     

Co-ordinated gene expression during phases of dormancy release in raspberry (Rubus idaeus L.) buds

Bud break in raspberry (Rubus idaeus L.) is often poor and uneven, with many of the subapical buds remaining in a dormant state. In order to determine the dormancy status of raspberry buds, an empirical measure of bud burst in a growth-permissive environment following exposure to chilling (4 degrees C cold storage) was developed. For cv. Glen Ample, percentage bud burst in intact canes and isolated nodes was recorded after 14 d. Isolated nodes (a measure of endodormancy) achieved 100% bud burst after approximately 1500 h chilling whereas buds on intact plants (combined endo- and paradormancy) required an additional 1000 h chilling. A microarray approach was used to follow changes in gene expression that occurred during dormancy transition. The probes for the microarrays were obtained from endodormant and paradormant raspberry bud cDNA libraries. The expression profiles of 5300 clones from these libraries were subjected to principal component analysis to determine the most significant expression patterns. Sequence analysis of these clones, in many cases, enabled their functional categorization and the development of hypotheses concerning the mechanisms of bud dormancy release. Thus a set of novel candidates for key dormancy-related genes from raspberry buds have been identified. Bud dormancy is fundamental to the study of plant developmental processes and, in addition, its regulation is of significant economic importance to fruit and horticultural industries.     

The molecular basis of photoperiodism

The rotation of our planet results in regular changes in environmental cues such as daylength and temperature, and organisms have evolved a molecular oscillator that allows them to anticipate these changes and adapt their development accordingly. In many plants, the transition from vegetative to reproductive growth is controlled by photoperiod, which synchronises flowering with favourable seasons of the year. Here, we describe the notable progress that has been made in identifying the molecular mechanisms that measure daylength and control of flowering time in Arabidopsis, a long day (LD) plant, and in rice, a short day (SD) plant. Although the components of the Arabidopsis regulatory network seem to be conserved in other species, the difference in the function of particular genes may contribute to the reverse response to daylength observed between LD and SD plants. We also highlight the recent advances in understanding the regulatory mechanisms that underlie other developmental transitions controlled by photoperiod, including tuberisation and the onset of dormancy in the buds of perennial plants.     

Opposite effects of daylength and temperature on flowering and summer dormancy of Poa bulbosa

BACKGROUND AND AIMS: The timing of flowering and summer dormancy induction plays a central role in the adaptation of Mediterranean geophytes to changes in the length of the growth season along rainfall gradients. Our aim was to analyse the role of the variation in the responses of flowering and summer dormancy to vernalization, daylength and growth temperature for the adaptation of Poa bulbosa, a perennial geophytic grass, to increasing aridity. METHODS: Flowering and dormancy were studied under controlled daylengths [9 h short day (SD) vs. 16 h long day (LD)] and temperatures (16/10, 22/16 and 28/22 degrees C day/night) in four ecotypes originating in arid, semi-arid and mesic habitats (110, 276 and 810 mm rain year(-1), respectively) and differing in flowering capacity under natural conditions: arid-flowering, semi-arid-flowering, semi-arid-non-flowering and mesic-non-flowering. KEY RESULTS: Flowering and dormancy were affected in opposite ways by daylength and growth temperature. Flowering occurred almost exclusively under SD. In contrast, plants became dormant much earlier under LD than under SD. In both daylengths, high temperature and pre-chilling (6 weeks at 5 degrees C) enhanced dormancy imposition, but inhibited or postponed flowering, respectively. Induction of flowering and dormancy in the different ecotypes showed differential responsiveness to daylength and temperature. Arid and semi-arid ecotypes had a higher proportion of flowering plants and flowering tillers as well as more panicles per plant than mesic ecotypes. 'Flowering' ecotypes entered dormancy earlier than 'non-flowering' ecotypes, while the more arid the site of ecotype origin, the earlier the ecotype entered dormancy. CONCLUSIONS: Variation in the flowering capacity of ecotypes differing in drought tolerance was interpreted as the result of balanced opposite effects of daylength and temperature on the flowering and dormancy processes.     

Interrelations between respiration and dormancy in buds of three hardwood species with different chilling requirements for dormancy release

 Respiration in vegetative buds of mature Betula pendula, Alnus glutinosa and Prunus padus trees was measured monthly at 15°C from mid-October 1996 to natural outdoor budburst in April 1997. In B. pendula the effect of bud water content on respiration was also estimated (December–April) by artificial imbibition of buds for 24 h prior to measurement of respiration. For estimation of corresponding bud dormancy status, batches of twigs were forced at identical monthly intervals at 15°C in long days (24 h), and budburst recorded. In all species dormancy was deepest when the leaves were shed in October, and dormancy was first alleviated in P. padus followed by B. pendula and A. glutinosa. However, bud respiration capacity was not related to dormancy release as it decreased in all species from October to November and displayed no notable increase until February in P. padus, March in B. pendula and April in A. glutinosa, after completion of dormancy release. Rather, increase in respiration coincided with growth resumption prior to budburst. Artificial imbibition of B. pendula buds increased the water content by approximately 10% (FW) and induced a doubling of the respiration rate (December–February). Moreover, the seasonal variation in bud water content (October–April) explained 94% of the variation in respiration in B. pendula and P. padus, and 84% in A. glutinosa. These observations suggest an important role of water content for respiration. During a cold period from mid-December to mid-January with mean temperature of –9.7°C dormancy release was arrested in P. padus, and to some degree in A. glutinosa, whereas dormancy release progressed normally in B. pendula. This indicates species differences in lower critical temperatures for dormancy release. Received: 30 June 1997 / Acceped: 1 October 1997     

Intensity of Bud Dormancy in Douglas-fir and Its Relation to Scale Removal and Rooting Ability

Uniform 1- or 2-year-old rooted cuttings of 3 Douglas-fir, Pseudotsuga menziesii (Mirb.) Franco, clones were grown under natural conditions in containers from July 1, 1971 to February 15, 1972. At 2-week intervals, plants from this natural temperature and daylength environment were moved into controlled, long day (LD-18 h) and short day (SD-9 h) environments to measure the intensity of bud dormancy from its inception to termination based on number of days to bud break and percentage of expanding buds on a given date. Growth responses to bud scale removal were also helpful in describing the degree and nature of bud dormancy. The cessation of initiatory activity at the bud apex, reflected in the needle number of the subsequent growth flush, corresponded to a September peak of bud dormancy based on the number of days to bud break in the LD environment. Similarly, the cold requirement for breaking bud dormancy was measurable in the SD environment. The use of such rest intensity indices is illustrated in the close relationship established between bud dormancy development and stem cutting rooting ability.     

Influences of daylength and temperature on the period of diapause and its ending process in dormant larvae of burnet moths (Lepidoptera,Zygaenidae)

The onset of larval diapause in the burnet moth Zygaena trifolii is clearly characterized by the larva molting into a specialized dormant morph. In a potentially bivoltine Mediterranean population (Marseille) two types of diapause can occur within 1 year: firstly, a facultative summer diapause of 3–10 weeks, and secondly, an obligate winter diapause, which can be lengthened by a period of thermal quiescence to several months in temperatures of 5°C. For the first time, three successive physiological periods have been experimentally distinguished within an insect dormancy (between onset of diapause and molting to the next non-diapause stage), using chilling periods of 30–180 days at 5°C, and varying conditions of photoperiod and temperature. These stages are: (1) a continuous Diapause-ending process (DEP); (2) thermal quiescence (Q); and finally, (3) a period of postdiapause development (PDD) before molting to the next larval instar. The result of transferring dormant larvae from chilling at 5°C to 20°C depended on the length of the chilling period. After chilling for 120–180 days, molting to the next instar occurred after 6–10 days, independent of daylength. This period corresponds with the duration of PDD. After shorter chilling periods (90, 60, 30 days and the control, 0 days) the period to eclosion increased exponentially, and included both the latter part of the previous diapause process and the 6–10 day period of PDD. However, photoperiod also influences the time to eclosion after chilling. Short daylength (8 h light / 16 h dark: LD 8/16) lengthened the diapause in comparison to long daylength (16 h light / 8 h dark: LD 16/8). Short daylength had a similar effect during chilling at 5°C, as measured by the longer time to eclosion after transfer. The shorter time to eclosion resulting from longer chilling periods (30–90 days) demonstrates that the state of diapause is continuously shortened at 5°C, and corresponds to the neuroendocrine controlled DEP. Presumably the DEP has already started after the onset of diapause. When chilling was continued after the end of the DEP, which ranged between 90 and 120 days, thermal quiescence (Q) followed (observed maximum 395 days). Different photoperiodic conditions during the pre-diapause inductive period modified diapause intensity (measured as the duration of diapause), in that a photoperiodic signal just below the critical photoperiod for diapause induction (LD 15/9) intensified diapause. Experiments simulating the summer diapause showed that PDD occurred in the range of 10–25°C. Higher temperatures (15 and 20°C) shortened the DEP at LD 16/8, so that at 20°C many individuals had already terminated diapause after 10–40 days and had molted after the 6–10 days of PDD. A temperature of 25°C unexpectedly lengthened the DEP to 110 days in several individuals. The ecological consequences and the adaptive significance of variation in the duration of the diapause are discussed in relation to the persistence of local populations predictably variable and rare climatic extremes throughout the year.     

Abscisic acid, indole-3-acetic acid and cytokinin changes in buds of Pseudotsuga menziesii during bud quiescence release

Bud quiescence release, considered as the ultimate dormancy breaking phase, was achieved in Pseudotsuga menziesii (Mirb.) Franco by a 9-week cold (5°C) treatment, under short daylength (9 h) followed by a transfer to mild temperature (22°C) under long daylength (16 h). Indole-3-acetic acid (IAA), abscisic acid (ABA), zeatin-type (Z) and isopentenyladenine-type (iPA) cytokinin (CK) levels were measured by means of an ELISA technique performed on HPLC-fractionated extracts of terminal and axillary buds. During the cold period, all hormones except IP-type CK levels decreased, whereas the opposite observation was made after transfer to mild temperature and long daylength, when buds started to grow. Some other immunoreactive compounds were also detected and quantified. The ABA-glucosyl ester (ABA-GE) level pattern was similar to that of ABA, but no accumulation occurred at mild temperatures. A putative IAA conjugate, more polar than IAA, was also detected. Its level increased transiently like IAA in terminal buds and, to a lesser extent, in axillary buds during the 10th week of the experiment. In terminal buds, isopentenyladenosine ([9R]-iP) was released by alkaline hydrolysis of a polar immunoreactive compound detected with anti-[9R]iP antibodies. This compound accumulated during the cold period and quickly dropped at 22°C. Relationships between environmental conditions and endogenous hormones are discussed.     

Regeneration from rhizome fragments of Agropyron repens

Experiments were done with rhizome fragments of Agropyron repens with or without ‘late spring dormancy’. Increasing concentrations of KN0₃ from 1 to 210 ppm successively increased the percentage of buds released from dormancy, but the restriction of shoot extension was significantly lessened only when concentrations of nitrogen were 50 ppm or more. Solutions of sodium nitrite, ammonium chloride and glutamic acid with equal nitrogen contents were equally effective in releasing buds from dormancy. Larger amounts of nitrogen were required to stimulate growth in basal buds, than in apical buds. GA₃, and chilling at – 2 ^oC slightly increased the percentage of buds growing but did not significantly affect the amount of extension growth, while ethephon (2-chloroethylphosphonic acid) had no effect. The restoration of regenerative capacity was associated with increased utilization of rhizome sugars. In single-node rhizome fragments with ‘late spring dormancy’, chilling for 2 wk slightly increased the regenerative capacity but chilling for longer periods decreased it, possibly because respiration during the protracted period of chilling depleted rhizome reserves. Chilling also increased the utilization of rhizome carbohydrates during subsequent growth. Node position affected regenerative capacity: buds from the apical end of the rhizomes were found to have the highest regenerative capacity, this being associated with their greater nitrogen content. Because the name ‘late spring dormancy’ seems to be inappropriate for this phenomena, the term ‘Restricted Regenerative Capacity’ is proposed.     

Dormancy in peach (Prunus persica L.) flower buds

Morphological studies were carried out with peach flower buds collected monthly in 1989 and 1990, from two months before leaf fall (7 March) until two to three weeks before bloom (7/8 August). Chilled (2–4°C for 30 days) and unchilled buds were exposed to 20 to 25°C, 100% RH and continuous light. Gibberellin A₃ (3 ng or 30 ng) was applied to some of the non-chilled cuttings at three days intervals. Then, 12, 19, and 26 days after they were planted, the buds were sampled and processed for histological studies. Cultured flower buds (chilled or unchilled) had accelerated anther and gynoecium morphogenesis after 12 days under controlled conditions, compared to buds processed immediately after collection from the field. Chilling treatment augmented the bud culture effect, while Gibberellin A₃ applications to the excised buds retarded bud morphogenesis to a stage comparable to that of buds collected directly from the field. This, suggests that the comparatively high levels of Gibberellin A_1/3 we previously found in mid winter [15, 18] could be at least one of the factors that controls floral bud dormancy by retarding anther and gynoecium development.     

Chilling outweighs photoperiod in preventing precocious spring development

It is well known that increased spring temperatures cause earlier onset dates of leaf unfolding and flowering. However, a temperature increase in winter may be associated with delayed development when species' chilling requirements are not fulfilled. Furthermore, photosensitivity is supposed to interfere with temperature triggers. To date, neither the relative importance nor possible interactions of these three factors have been elucidated. In this study, we present a multispecies climate chamber experiment to test the effects of chilling and photoperiod on the spring phenology of 36 woody species. Several hypotheses regarding their variation with species traits (successional strategy, floristic status, climate of their native range) were tested. Long photoperiods advanced budburst for one‐third of the studied species, but magnitudes of these effects were generally minor. In contrast to prior hypotheses, photosensitive responses were not restricted to climax or oceanic species. Increased chilling length advanced budburst for almost all species; its effect greatly exceeding that of photoperiod. Moreover, we suggest that photosensitivity and chilling effects have to be rigorously disentangled, as the response to photoperiod was restricted to individuals that had not been fully chilled. The results indicate that temperature requirements and successional strategy are linked, with climax species having higher chilling and forcing requirements than pioneer species. Temperature requirements of invasive species closely matched those of native species, suggesting that high phenological concordance is a prerequisite for successful establishment. Lack of chilling not only led to a considerable delay in budburst but also caused substantial changes in the chronological order of species' budburst. The results reveal that increased winter temperatures might impact forest ecosystems more than formerly assumed. Species with lower chilling requirements, such as pioneer or invasive species, might profit from warming winters, if late spring frost events would in parallel occur earlier.     

Photothermal control of the imposition of summer dormancy in Poabulbosa, a perennial grass geophyte

Poa bulbosa L., like many other Mediterranean geophytes, grows in the winter and enters a phase of summer dormancy in the spring. Summer dormancy enables these plants to survive the hot and dry summer. Long days are the main environmental factor active in the induction of summer dormancy in P . bulbosa and elevated temperatures accelerate dormancy development. P . bulbosa becomes dormant earlier than most other species that grow actively in the winter. Previous studies suggested that pre-exposure of P . bulbosa to short days and low temperatures during the autumn and early winter increased its sensitivity to photoperiodic induction in late winter, and thus enabled the early imposition of dormancy. To study this hypothesis, experiments were carried out under controlled photothermal conditions in the phytotron, under natural daylight extended with artificial lighting. The critical photoperiod for induction of summer dormancy at an optimal temperature (22/17°C day/night) was between 11 and 12 h. Photoperiods shorter than 12 h were noninductive, while 14- and 16-h days were fully inductive. A night break of 1 h of light given at the middle of the dark period of an 8-h photoperiod also resulted in full induction of dormancy. Pre-exposure to either low temperature (chilling at 5°C) or to short days of 8 h (SD) enhanced the inductive effect of subsequent 16-h long days (LD). The enhancing effect of chilling and SD increased with longer duration, i.e. fewer LDs were required to impose dormancy. However, the day-length during the low-temperature pretreatment had no effect on the level of induction at the following LD. Chilling followed by SD did not induce dormancy. The relevance of these responses to the development and survival of P . bulbosa in its natural habitat is discussed.