Depth Of Dormancy Research Articles

Effects of after-ripening, stratification and GA 3 on dormancy release and on germination of wild asparagus ( Asparagus acutifolius L.) seeds

Seeds of wild asparagus ( Asparagus acutifolius L.) were treated and compared in this research to investigate seed dormancy class and level involved in this species. Four seed lots were compared: (i) freshly harvested seeds in 2007 (07Fr); (ii) freshly harvested seeds in 2008 (08Fr); (iii) after-ripened (AR) 2007 seeds dry stored in glass jars (AR g); (iv) AR 2007 seeds dry stored in paper bags (AR p). The 07Fr seeds were exposed to (1) chemical scarification combined with gibberellic acid (GA 3) levels (0, 200, 400, and 600 mg L −1) and to (2) 28-day moist stratification at 5 and 23 °C, and two sequences of 5/23 °C combined with 0 and 400 GA 3 mg L −1 levels, and (3) together to the 08Fr and AR seeds were exposed to 56-day moist stratification at 5, 23, or 5/23 °C. With the 08Fr and AR seed lots this last stratification treatment was combined with 0 or 800 GA 3 mg L −1 levels. The dormancy depth of 08Fr (32% germination) was less than 07Fr seeds (2%). The latter after-ripened during dry storage and when stored in glass germinated more (47.5%) than in paper (12%). Stratification for 4 weeks was ineffective in improving germination of 07Fr seeds; when chemically scarified they did not germinate at all. The highest (nearly 70%) and the most rapid and uniform germination were observed for all the lots when they were warm stratified for 56 days. Warm stratification improved germination more than alternate temperature stratification, while cold stratification inhibited germination especially for the 08Fr and ARg lots, thus seeds seem not to have a morphological component to their dormancy. GA 3 only improved germination of 07Fr seeds, at a low rate. A. acutifolius seeds fit the characteristics of a non-deep physiological dormancy.

Light and temperature sensing and signaling in induction of bud dormancy in woody plants

In woody species cycling between growth and dormancy must be precisely synchronized with the seasonal climatic variations. Cessation of apical growth, resulting from exposure to short photoperiod (SD) and altered light quality, is gating the chain of events resulting in bud dormancy and cold hardiness. The relative importance of these light parameters, sensed by phytochromes and possibly a blue light receptor, varies with latitude. Early in SD, changes in expression of light signaling components dominate. In Populus active shoot elongation is linked to high expression of FLOWERING LOCUS T (FT) resulting from coincidence of high levels of CONSTANS and light at the end of days longer than a critical one. In Picea, PaFT4 expression increases substantially in response to SD. Thus, in contrast to Populus-FT, PaFT4 appears to function in inhibition of shoot elongation or promotion of growth cessation. Accordingly, different FT-genes appear to have opposite effects in photoperiodic control of shoot elongation. Reduction in gibberellin under SD is involved in control of growth cessation and bud formation, but not further dormancy development. Coinciding with formation of a closed bud, abscisic acid activity increases and cell-proliferation genes are down-regulated. When dormancy is established very few changes in gene expression occur. Thus, maintenance of dormancy is not dependent on comprehensive transcriptional regulation. In some species low temperature induces growth cessation and dormancy, in others temperature affects photoperiod requirement. The temperature under SD affects both the rate of growth cessation, bud formation and depth of dormancy. As yet, information on the molecular basis of these responses to temperature is scarce.

Characterization of dormancy behaviour in seeds of the model legumeMedicago truncatula

AbstractSeeds ofMedicago truncatula, a genomic model species for legumes, exhibit physiological and physical dormancy. Here, the factors influencing the germination behaviour of freshly harvested and stored seeds were investigated using several genotypes. Hardseededness is promoted when mature seeds are equilibrated at relative humidities (RH) below 75%. The release of physical dormancy during imbibition was dependent on the initial water content/RH that the seeds were dried to: the drier the seeds, the longer the imbibition time needed to break physical dormancy. The kinetics of physical dormancy release was slower than that of physiological dormancy, making it possible to uncouple both phenomena. Freshly harvested embryos without seed coverings germinated at the same speed as afterripened seeds. The depth of dormancy varied between differentM. truncatulagenotypes, from more to less dormant: DZA315.16>A17 (Jemalong)>R108>DZA45.5. This difference was eliminated by removing the endosperm. Collectively, these observations indicate that the endosperm is likely the main factor in the reduced germination of freshly harvested seeds. White light decreased germination speed of dormant seeds whereas it had no effect on non-dormant seeds. Recently harvested seeds were most dormant at temperatures above 17°C, whereas afterripened seeds germinated over a wider range of temperature. Fluridone could efficiently break dormancy, reinforcing the role of abscisic acid (ABA) synthesis. However, dormancy was not affected by gibberellic acid (100 μM GA3) or nitrate. The particular dormancy features unravelled here forM. truncatula, combined with the available genomic resources, make it a new, useful model for genetic and molecular studies which can complement those developed for Arabidopsis.

겨울기온 상승에 따른 복숭아 나무 '장호원황도' 품종의 결과지에 대한 동상해위험 공간분석: II. 휴면심도로 표현한 생리적 내동성에 근거한 동해위험지수

복숭아 나무 '장호원황도' 품종의 결과지에 대한 월동기간 중 생리적 내한성을 가리키는 지표로서 일별 기온에 의해 계산되는 휴면심도를 설정하였다. 휴면심도 추정모형의 최적모수(기준온도, 저온요구도)를 도출하기 위해 2008-2009 겨울 동안 총 12회에 걸친 실험을 수행한 결과, 내생휴면해제에 필요한 '장호원황도'의 기준온도 <TEX>$5.7^{\circ}C$</TEX>와 저온요구도 -108을 얻었다. 1992-2008년 기간 중 수원기상대 일 최고 및 최저기온자료를 이용하여 이 모형에 의해 '장호원황도'의 만개기를 예측하고 기존의 DVS모형과 회귀모형에 의한 예상 만개기와 비교한 결과 이 모형의 예측능력이 우수하였다. 이 모형에 의해 추정된 휴면심도를 선행연구에서 얻은 동해유발온도와 결합하여 동해위험확률을 계산할 수 있는 경험식을 도출하였다. 날짜와 최저기온이 주어지면 이 식에 의해 '장호원황도'의 갈변이나 발아장해 등 동해증상이 나타날 수 있는 확률, 즉 동해위험 지수를 미리 알 수 있으므로 복숭아 재배농가의 동해 경감에 기여할 것으로 기대된다. In order to predict the risk of freeze injury for 'Changhowon Hwangdo' peach trees, we used the dormancy depth (i.e., the daily chill unit accumulation during the overwintering period) as a proxy for the short-term, physiological tolerance to freezing temperatures. A Chill-days model was employed and its parameters such as base temperature and chilling requirement were optimized for peach trees based on the 12 observational experiments during the 2008-2009 winter. The model predicted the flowering dates much closer to the observations than other models without considering dormancy depth, showing the strength of employing dormancy depth into consideration. To derive empirical equations for calculating the probabilistic freeze risk, the dormancy depth was then combined with the browning ratio and the budburst ratio of frozen peach fruit branches. Given the exact date and the predicted minimum temperature, the equations calculate the probability of freeze damages such as a failure in budburst or tissue browning. This method of employing dormancy depth in addition to freezing temperature would be useful in locating in advance the risky areas of freezing injury for peach trees production under the projected climate change.

겨울기온 상승에 따른 복숭아 나무 '장호원황도' 품종의 결과지에 대한 동상해위험 공간분석: III. 고해상도 기후시나리오에 근거한 동해위험의 미래분포

The geographical distribution of freeze risk determines the latitudinal and altitudinal limits and the maximum acreage suitable for fruit production. Any changes in its pattern can affect the policy for climate change adaptation in fruit industry. High-definition digital maps for such applications are not available yet due to uncertainty in the combined responses of temperature and dormancy depth under the future climate scenarios. We applied an empirical freeze risk index, which was derived from the combination of the dormancy depth and threshold temperature inducing freeze damage to dormant buds of `Changhowon Hwangdo` peach trees, to the high-definition digital climate maps prepared for the current (1971-2000), the near future (2011-2040) and the far future (2071-2100) climate scenarios. According to the geospatial analysis at a landscape scale, both the safe and risky areas will be expanded in the future and some of the major peach cultivation areas may encounter difficulty in safe overwintering due to weakening cold tolerance resulting from insufficient chilling. Our test of this method for the two counties representing the major peach cultivation areas in South Korea demonstrated that the migration of risky areas could be detected at a sub-grid scale. The method presented in this study can contribute significantly to climate change adaptation planning in agriculture as a decision aids tool.

Warm temperature accelerates short photoperiod-induced growth cessation and dormancy induction in hybrid poplar (Populus × spp.)

There is increasing evidence that temperature, in addition to photoperiod, may be an important factor regulating bud dormancy. The impact of temperature during growth cessation, dormancy development, and subsequent cold acclimation was examined in four hybrid poplar clones with contrasting acclimation patterns: ‘Okanese’—EARLY, ‘Walker’—INT1, ‘Katepwa’—INT2, and ‘Prairie Sky’—LATE. Four day–night temperature treatments (13.5/8.5, 18.5/13.5, 23.5/8.5, and 18.5/3.5°C) were applied during a 60-day induction period to reflect current and predicted future annual variation in autumn temperature for Saskatoon, SK. Warm night temperature (18.5/13.5°C) strongly accelerated growth cessation, dormancy development, and cold acclimation in all four clones. Day temperature had the opposite effect of night temperature. Day and night temperatures appeared to act antagonistically against each other during growth cessation and subsequent dormancy development and cold acclimation. Growth cessation, dormancy development, and cold acclimation in EARLY and LATE were less affected by induction temperature than INT1 and INT2 suggesting that genotypic variations exist in response to temperature. Separating specific phenological stages and the impact by temperature on each clone revealed the complexity of fall phenological changes and their interaction with temperature. Most importantly, future changes in temperature may affect time to growth cessation, subsequently altering the depth of dormancy and cold hardiness in hybrid poplar.

Photoperiod modifies the diurnal expression profile of VvPHYA and VvPHYB transcripts in field-grown grapevine leaves

Despite the crucial role that phytochromes (Phys) play in light perception and in the entrainment of the circadian clock to local time, the photoperiodic regulation of PHYA and PHYB gene expression has been poorly studied, especially in woody perennials. Here the dynamic of Vitis vinifera PHYA (VvPHYA) and PHYB (VvPHYB) transcript accumulation was studied in field-grown grapevine leaves throughout daily cycles under decreasing natural photoperiods. Given that in grapevine the entrance of buds into endodormancy (ED) is a photoperiod-driven process, increases in BR(50) values, a parameter that measures the depth of dormancy in single bud cuttings assays was used to determine the critical daylength at which grapevine discriminates between long day (LD) and short day (SD) photoperiod. Therefore, we monitored the daily expression profile of VvPHYA and VvPHYB transcripts before, during and after the defined critical daylength. Results showed that under LD photoperiod (21 December, daylength 14 h 40 min) the abundance of both transcripts oscillated with diurnal rhythms, attaining maximum and minimum levels before dawn and after dusk, respectively. However, under SD photoperiod (12 April, daylength 11 h 40 min) the rhythmic expression disappeared, and both transcripts expressed uniformly at high levels. Our results showing that photoperiod regulates VvPHYA and VvPHYB gene expression, contrast with those reported in Arabidopsis and in other herbaceous plants in which PHYA and PHYB gene expression is regulated by the circadian clock.

최저기온과 휴면심도 기반의 동해위험도를 활용한 'Campbell Early' 포도의 내동성 지도 제작

최저기온과 휴면심도 기반의 동해위험도를 활용한 'Campbell Early' 포도의 내동성 지도 제작

The relationship between pyridine nucleotides and seed dormancy

To investigate the proposed role for NAD metabolism in regulating seed dormancy, NAD metabolites and associated enzyme activities were analysed in seed of Arabidopsis thaliana ecotypes ranging from Col-0, which has low seed dormancy, to Cvi, which is highly dormant. Seed poly(ADP-ribosyl)ation levels did not correlate well with the depth of seed dormancy but did correlate with the sensitivity of germination to the DNA damaging agent MMS. Cvi seed had relatively high NAD and low NADP levels compared with the less dormant ecotypes and the NAD : NADP ratios correlated well with dormancy. The activity of NAD kinase was relatively low, and NADP phosphatase was relatively high in dormant Cvi seed, indicating that these enzymes may be involved in controlling the NAD : NADP ratio. Dormant fresh Cvi and nondormant after-ripened Cvi seeds were used to investigate further. Measurement of reduced and oxidised pyridine nucleotides indicated that breaking of dormancy was associated with a reduction in NAD levels but not with an increase in NADP levels. It is proposed that poly(ADP-ribose) polymerase is involved in protecting the seed from genotoxic stress, whereas the level of NAD affects the depth of dormancy, perhaps by enhancing abscisic acid (ABA) synthesis.

남한의 겨울기온 상승 예측에 따른 포도 "캠벨얼리" 품종의 단기 내동성 변화 전망

Warming trends during winter seasons in East Asian regions are expected to accelerate in the future according to the climate projection by the Inter-governmental Panel on Climate Change (IPCC). Warmer winters may affect short-term cold hardiness of deciduous fruit trees, and yet phenological observations are scant compared to long-term climate records in the regions. Dormancy depth, which can be estimated by daily temperature, is expected to serve as a reasonable proxy for physiological tolerance of flowering buds to low temperature in winter. In order to delineate the geographical pattern of short-term cold hardiness in grapevines, a selected dormancy depth model was parameterized for "Campbell Early", the major cultivar in South Korea. Gridded data sets of daily maximum and minimum temperature with a 270m cell spacing ("High Definition Digital Temperature Map", HDDTM) were prepared for the current climatological normal year (1971-2000) based on observations at the 56 Korea Meteorological Administration (KMA) stations and a geospatial interpolation scheme for correcting land surface effects (e.g., land use, topography, and site elevation). To generate relevant datasets for climatological normal years in the future, we combined a 25km-resolution, 2011-2100 temperature projection dataset covering South Korea (under the auspices of the IPCC-SRES A2 scenario) with the 1971-2000 HD-DTM. The dormancy depth model was run with the gridded datasets to estimate geographical pattern of change in the cold-hardiness period (the number of days between endo- and forced dormancy release) across South Korea for the normal years (1971-2000, 2011-2040, 2041-2070, and 2071-2100). Results showed that the cold-hardiness zone with 60 days or longer cold-tolerant period would diminish from 58% of the total land area of South Korea in 1971-2000 to 40% in 2011-2040, 14% in 2041-2070, and less than 3% in 2071-2100. This method can be applied to other deciduous fruit trees for delineating geographical shift of cold-hardiness zone under the projected climate change in the future, thereby providing valuable information for adaptation strategy in fruit industry.

Using Thermal Time to Simulate Dormancy Depth and Bud-Burst of Vineyards in Korea for the Twentieth Century

Abstract A winter-season warming trend has been observed in eastern Asian countries during the last century. Significant effects on dormancy and the subsequent bud-burst of deciduous fruit trees are expected. However, phenological observations are scant in comparison with long-time climate records in the region. Chill-day accumulation, estimated from daily maximum and minimum temperature, is a reasonable proxy for dormancy depth of temperate-zone fruit trees. A selected chill-day model was parameterized for the Campbell Early grapevine, which is the major cultivar (grown virtually everywhere) in South Korea. To derive model parameters (threshold temperature for chilling and the chilling requirement for breaking dormancy), a controlled-environment experiment using field-sampled twigs of Campbell Early was conducted. The chill-day model to estimate bud-burst dates was adjusted by derived parameters and was applied using 1994–2004 daily temperature data obtained from the automated weather station in the vineyard at the National Horticultural Research Institute. The model gave consistently good performance in predicting bud-burst of Campbell Early (RMSE of 2.5 days). To simulate dormancy depth of Campbell Early at eight locations in South Korea for the last century, the model was applied using data obtained for each location from 1921 to 2004. Calculations showed that the chilling requirement for breaking endodormancy of Campbell Early can be satisfied by mid-January to late February in South Korea, and the date was delayed going either northward or southward from the Daegu–Jeonju line that crosses the middle of South Korea in the east–west direction. Maximum length of the cold tolerant period (the number of days between endodormancy release and the forced dormancy release) showed the same spatial pattern. Dormancy release for 1981–2004 advanced by as much as 15 days relative to that for 1921–50 at all locations except Jeju (located in the southernmost island with a subtropical climate), where an average 15-day delay was predicted. The cold-tolerant period diminished somewhat at six out of eight locations. As a result, bud-burst of Campbell Early in spring was advanced by 6–10 days at most locations, and interannual variation in bud-burst dates increased at all locations. The earlier bud-burst after the 1970s was due to 1) warming in winter that results in earlier dormancy release (Incheon, Mokpo, Gangneung, and Jeonju), 2) warming in early spring that enhances regrowth after breaking dormancy (Busan and Jeju), and 3) a combination of both (Seoul and Daegu).

Phenotypic variation in caryopsis dormancy and seedling salt tolerance in wild barley, Hordeum spontaneum, from different habitats in Israel

The phenotypic variation in caryopsis dormancy and seedling salt tolerance was investigated in 16 wild barley ecotypes in Israel. Depth of dormancy, as reflected by the time to maximum germination percentage, ranged from 15 to 103 days under dormancy-break treatment. Lower dormancy was characteristic of the mesic ecotypes, whereas deeper dormancy was characteristic of the xeric ecotypes. Dormancy-break patterns were revealed by growth curves: the xeric ecotype showed an S-shaped curve, whereas the mesic ecotype displayed a reverse L-shaped curve. Seedling salt tolerance was assessed by the ratio of root or coleoptile length in a seedling grown in 100 or 200 mM NaCl solution to that of a seedling grown in water. The root- and coleoptile-length ratios of mesic ecotypes were much higher than that of the xeric ecotypes, except that there was no observable difference in coleoptile-length ratio at 100 mM NaCl. The mesic ecotype was more tolerant to salt than the xeric ecotype at the young seedling stage, and seedling salt tolerance was negatively correlated with caryopsis dormancy depth. Thus evolutionary background environments have had a strong effect on the intensity of caryopsis dormancy in wild barley. Through natural selection, wild barley has adapted to dry and hot environments by increasing dormancy but not young seedling salt tolerance.

Detection of seed dormancy QTL in multiple mapping populations derived from crosses involving novel barley germplasm

Seed dormancy is one of the most important traits in germination process to control malting and pre-harvest sprouting in barley (Hordeum vulgare L.). EST based linkage maps were constructed on seven recombinant inbred (RI) and one doubled haploid (DH) populations derived from crosses including eleven cultivated and one wild barley strains showing the wide range of seed dormancy levels. Seed dormancy of each RI and DH line was estimated from the germination percentage at 5 and 10 weeks post-harvest after-ripening periods in 2003 and 2005. Quantitative trait loci (QTLs) controlling seed dormancy were detected by the composite interval mapping procedure on the RI and DH populations. A total of 38 QTLs clustered around 11 regions were identified on the barley chromosomes except 2H among the eight populations. Several QTL regions detected in the present study were reported on similar positions in the previous QTL studies. The QTL on at the centromeric region of long arm of chromosome 5H was identified in all the RI and DH populations with the different degrees of dormancy depth and period. The responsible gene of the QTL might possess a large allelic variation among the cross combinations, or can be multiple genes located on the same region. The various loci and their different effects in dormancy found in the barley germplasm in the present study enable us to control the practical level of seed dormancy in barley breeding programs.

Seed dormancy release in Arabidopsis Cvi by dry after‐ripening, low temperature, nitrate and light shows common quantitative patterns of gene expression directed by environmentally specific sensing

The depth of seed dormancy can be influenced by a number of different environmental signals, but whether a common mechanism underlies this apparently similar response has yet to be investigated. Full-genome microarrays were used for a global transcript analysis of Arabidopsis thaliana Cape Verde Island accession seeds exposed to dry after-ripening (AR), or low temperature, nitrate and light when imbibed. Germination studies showed that the sensitivity of imbibed seeds to low temperature, nitrate and light was dependent upon the length of time spent AR following harvest. Seeds had an absolute requirement for light to complete dormancy release in all conditions, but this effect required an exposure to a prior dormancy relieving environment. Principal component analyses of the expression patterns observed grouped physiological states in a way that related to the depth of seed dormancy, rather than the type of environmental exposure. Furthermore, opposite changes in transcript abundance of genes in sets associated with dormancy, or dormancy relief through AR, were also related to the depth of dormancy and common to different environments. Besides these common quantitative changes, environment-specific gene expression patterns during dormancy relief are also described. For example, higher transcript abundance for genes linked to the process of nitrate accumulation, and nitrate reduction was associated with dormancy relief. The quantity of GA3ox1 transcripts increased during dormancy relief in all conditions, in particular when dormancy relief was completed by exposure to light. This contrasts with transcripts linked to abscisic acid (ABA) synthesis, which declined. The results are consistent with a role for the ABA/gibberellic acid balance in integrating dormancy-relieving environmental signals.

Dormancy of alpine and subalpine perennial forbs.

Depth of dormancy of alpine and subalpine perennial forbs in autumn was investigated, which was judged by the number of days required for growth initiation at 24 °C. The depth of dormancy differed depending on Raunkiaer's life‐form and shoot habits. Chamaephytes with perennial shoot‐axes showed shallower dormancy than hemicryptophytes with annual shoot‐axes, and geophytes with annual shoot‐axes showed the deepest dormancy. The results strongly suggest that the dormancy is more endogenously controlled in forbs less hardy to freezing stress. Potential growth ability of alpine herbaceous chamaephytes in autumn is an adaptive advantage, since they utilize the short vegetative period as long as possible. All of the species with annual shoot‐axes had winter buds covered with scales. In plants with perennial shoot‐axes, percentage of winter buds covered with scales increased with increasing depth of dormancy. The results indicate that the shoot apices are well protected by bud scales in forbs with a long endogeneous‐dormant period.

Embryonic dormancy persists in the calli derived from apple embryo

Growth rate and differentiation ability of calli obtained form apple embryos depended on the depth of embryo dormancy and on the organ of callus origin. We wanted to answer whether some dormancy – related metabolic activities persist also in calli and whether they are affected by the dormancy status. The activities of invertases and proteases were determined in the calli obtained from axes and cotyledons of embryos after different periods of cold stratification. Patterns of changes in activities of alkaline invertase, albumine hydrolysing protease and cystine-aminopeptydase in extracts of different calli corresponded precisely to changes of these activities in axes and cotyledons of intact embryos submitted to stratification. These findings indicate that embryonic dormancy persists in undifferentiated cells of calli. The involvement of an unknown factor responsible for maintenance of the dormancy, which is transmitted to daughter cells during callus growth is suggested.

Ultrastructure of Pollen Grains from Forced and Unforced Shrubs of Common Lilac

Forcing makes possible to induce plant flowering independently of the season. In lilac, high temperature is the factor that breaks deep dormancy. The deepest dormancy occurs between the end of October and the end of December. Depending on the depth of dormancy, the starting temperatures required for forcing are 37°C in November, 31°C in December, and 25°C in January–March. Under natural conditions, the temperature inducing the inflorescence bud breaking is 6°C, whereas 9°C and 13°C or more allow inflorescence elongation and flowering, respectively (Kronenberg, 1994). In the present work, the effect of high temperature at the beginning of the forcing cycle on the structure of developing pollen grains of common lilac was investigated. Pollen grains from the outdoor-grown (control) shrubs showed no signs of degeneration. They were spherical, three-colpate to colporoidate, and bicellular, and contained large numbers of lipid bodies. High temperatures at the early forcing cycle (November) resulted in the degeneration of most microspores. The first signs of degeneration (cytoplasm plasmolysis) were observed at the tetrad stage and in mature anthers; the microspores consisted only of the outer and inner sporopolenin layers.

Relationship between floral evocation and bud dormancy in Satsuma mandarin

Satsuma mandarin trees are induced to flower by exposure to a low temperature in the fall, but the buds after floral evocation cannot grow in winter. Flowering is hastened by warming the trees in a greenhouse, but the number of floral buds is reduced when this is done before the completion of floral evocation. Thus, it is important to determine the time of floral evocation in citriculture, especially for citrus cultivars grown in a greenhouse. To determine the time of floral evocation in ‘Aoshima’ Satsuma mandarin ( Citrus unshiu Marc.), we sampled the vegetative shoots from non-bearing trees in each month from August to March of the next year, and examined flower bud formation on the shoot at 32 °C and 80% relative humidity (32 °C/80RH). The buds after floral evocation develop floral buds within a few days at 32 °C/80RH, and we can estimate the time of floral evocation from the time when the shoots sampled from the tree rapidly flower at 32 °C/80RH. The experiments conducted for 5 successive years from August 1998 to March 2003 showed that the time of floral evocation estimated by the above method varied with the year; from mid-November to mid-December in 2000 and from early February to late February in 1998. There was a close correlation between the flowering percentage of the buds on the shoot at 32 °C/80RH, and the days to sprouting on the shoot at 32 °C/80RH, which shows the depth of bud dormancy, although the time of floral evocation greatly varied with the year. Thus, the number of days to sprouting at 32 °C/80RH is a good indicator of floral evocation.

Effect of Temperature on the Induction of Bud Dormancy in Ecotypes of Betula pubescens and Betula pendula

The purpose of this study was to determine the influence of temperature applied during short day-induced budset on induction of dormancy in six ecotypes of Betula pubescens Ehrh. and two ecotypes of Betula pendula Roth. Seedlings were grown in a phytotron at constant temperatures of 9–21°C under a 12 h photoperiod (SD) during dormancy induction. Induction of dormancy was monitored by following bud flushing and shoot growth after transfer to long photoperiod conditions (24 h) at 18°C. Chilling requirement was studied in seedlings exposed to 10 weeks of SD. In both species induction of bud dormancy developed most rapidly at 15–18°C, and both 9–12°C and 21°C delayed the induction of dormancy. Raising the temperature (from 9 to 21°C) applied during induction of dormancy significantly increased the chilling requirement. These responses were noted for all ecotypes tested, but in general the northern ecotypes entered dormancy more quickly than the southern ones. No such trend was recorded for chilling requirement, although a B. pubescens ecotype from Iceland and another from the coast of northern Norway appeared to require a longer chilling treatment than the other ecotypes. In conclusion, induction and depth of bud dormancy in birch are significantly affected by temperature conditions and these effects may explain some of the annual variation in dormancy and chilling requirement observed in nature.

Effect of Temperature on the Induction of Bud Dormancy in Ecotypes of Betula pubescens and Betula pendula

The purpose of this study was to determine the influence of temperature applied during short day-induced budset on induction of dormancy in six ecotypes of Betula pubescens Ehrh. and two ecotypes of Betula pendula Roth. Seedlings were grown in a phytotron at constant temperatures of 9–21°C under a 12 h photoperiod (SD) during dormancy induction. Induction of dormancy was monitored by following bud flushing and shoot growth after transfer to long photoperiod conditions (24 h) at 18°C. Chilling requirement was studied in seedlings exposed to 10 weeks of SD. In both species induction of bud dormancy developed most rapidly at 15–18°C, and both 9–12°C and 21°C delayed the induction of dormancy. Raising the temperature (from 9 to 21°C) applied during induction of dormancy significantly increased the chilling requirement. These responses were noted for all ecotypes tested, but in general the northern ecotypes entered dormancy more quickly than the southern ones. No such trend was recorded for chilling requirement, although a B. pubescens ecotype from Iceland and another from the coast of northern Norway appeared to require a longer chilling treatment than the other ecotypes. In conclusion, induction and depth of bud dormancy in birch are significantly affected by temperature conditions and these effects may explain some of the annual variation in dormancy and chilling requirement observed in nature.