首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 46 毫秒
1.
Myking T  Heide OM 《Tree physiology》1995,15(11):697-704
Bud burst and dormancy release of latitudinal ecotypes of Betula pendula Roth and B. pubescens Ehrh. from Denmark ( approximately 56 degrees N), mid-Norway ( approximately 64 degrees N) and northern Norway ( approximately 69 degrees N) were studied in controlled environments. Dormant seedlings were chilled at 0, 5 or 10 degrees C from October 4 onward and then, at monthly intervals from mid-November to February, batches of seedlings were held at 15 degrees C in an 8-h (SD) or 24-h (LD) photoperiod to permit flushing. A decline in days to bud burst occurred with increasing chilling time in all ecotypes. In November, after 44 chilling days, time to bud burst was least in plants chilled at 0 and 5 degrees C. The difference diminished with increasing chilling time, and in February, after 136 chilling days, bud burst was earliest in plants chilled at 10 degrees C. Long photoperiods during flushing significantly reduced thermal time after short chilling periods (44 and 74 days), but had no effect when the chilling requirement was fully met after 105 or more chilling days. No significant difference in these responses was found between the two species. In both species, chilling requirement decreased significantly with increasing latitude of origin. Bud burst was normal in seedlings overwintered at 12 degrees C, but was erratic and delayed in seedlings overwintered at 15 and especially at 21 degrees C, indicating that the critical overwintering temperature is between 12 and 15 degrees C. We conclude that there is little risk of a chilling deficit in birch under Scandinavian winter conditions even with a climatic warming of 7-8 degrees C. The likely effects of a climatic warming include earlier bud burst, a longer growing season and increased risk of spring frost injury, especially in high latitude ecotypes.  相似文献   

2.
Heide OM 《Tree physiology》2003,23(13):931-936
The effect of temperature during short-day (SD) dormancy induction was examined in three boreal tree species in a controlled environment. Saplings of Betula pendula Roth, B. pubescens Ehrh. and Alnus glutinosa (L.) Moench. were exposed to 5 weeks of 10-h SD induction at 9, 15 and 21 degrees C followed by chilling at 5 degrees C for 40, 70, 100 and 130 days and subsequent forcing at 15 degrees C in a 24-h photoperiod for 60 days. In all species and with all chilling periods, high temperature during SD dormancy induction significantly delayed bud burst during subsequent flushing at 15 degrees C. In A. glutinosa, high temperature during SD dormancy induction also significantly increased the chilling requirement for dormancy release. Field experiments at 60 degrees N with a range of latitudinal birch populations revealed a highly significant correlation between autumn temperature and days to bud burst in the subsequent spring. September temperature alone explained 20% of the variation between years in time of bud burst. In birch populations from 69 and 71 degrees N, which ceased growing and shed their leaves in August when the mean temperature was 15 degrees C, bud burst occurred later than expected compared with lower latitude populations (56 degrees N) in which dormancy induction took place more than 2 months later at a mean temperature of about 6 degrees C. It is concluded that this autumn temperature response may be important for counterbalancing the potentially adverse effects of higher winter temperatures on dormancy stability of boreal trees during climate warming.  相似文献   

3.
We investigated responses of northern and southern ecotypes of silver birch (Betula pendula Roth) to exogenous abscisic acid (ABA) under controlled environmental conditions to determine the role of ABA in cold acclimation and dormancy development. Abscisic acid was sprayed on the leaves and changes in freezing tolerance, determined by the electrolyte leakage test, and bud dormancy were monitored. Applied ABA induced cold acclimation but had no effect on growth cessation in seedlings grown in long day conditions (LD, 24-h photoperiod at 18 degrees C). It enhanced freezing tolerance and accelerated growth cessation in seedlings grown in short day conditions (SD, 12-h photoperiod at 18 degrees C), and slightly enhanced freezing tolerance in seedlings grown at low temperature (LT, 24-h photoperiod at 4 degrees C) in both ecotypes. There were distinct ecotypic differences in ABA-induced cold acclimation and dormancy development. The northern ecotype was more responsive to applied ABA than the southern ecotype, resulting in more rapid development of freezing tolerance in all treatments, and earlier dormancy development in SD. When plants were grown in a photoperiod just above the critical photoperiod for the ecotype (defined as the longest photoperiod that induces growth cessation), applied ABA caused growth cessation and dormancy development. Compared with ABA-treated seedlings grown in SD, dormancy development was delayed in ABA-treated seedlings exposed to a near-critical photoperiod, but even in this treatment dormancy developed faster in the northern ecotype than in the southern ecotype.  相似文献   

4.
Abstract

The response of common alder [Alnus glutinosa (L.) Gaertn.] and downy birch (Betula pubescens Ehrh.) seeds to germination temperature was examined following chilling and priming. Seeds of two seed lots of each species were subjected to combinations of chilling (4±1°C) and priming (20°C) treatments in fully imbibed (FI) state or a lower target seed moisture content (TMC) level (30% and 35% in alder and birch, respectively). After treatment, the seeds were allowed to germinate for 56 days at constant temperatures of 7.5, 10, 15, 20, 25 or 30°C. The response to temperature and pretreatment differed between species, but the effect was consistent in each seed lot within each species. In alder, the TMC seeds germinated well across the full range of temperatures, whereas there was an optimum temperature (22–23°C) for seeds given the FI pretreatment. Priming had no significant effect on the germination response of the TMC seeds in alder, but priming greatly improved germination in the FI seeds, especially at the lower germination temperatures (optimum 18–19°C). In contrast, in birch, the TMC seeds germinated better across the full temperature range, but the optimal germination temperature (15°C) was the same for all seed pretreatments. Priming improved germination in both the FI and TMC seeds in birch.  相似文献   

5.
Vegis has put forward the theory that the range of growth-promoting temperatures changes during the induction and the release of dormancy. We have tested the response of buds of Betula pubescens Ehrh. and B. pendula Roth. on temperature during the induction and release of dormancy. Betula seedlings were exposed to dormancy-inducing high-temperature and short-day conditions and subsequently to dormancy-releasing chilling conditions in darkness. To monitor the dormancy status of the seedlings, subsets of them were transferred to five forcing temperatures and their budburst was observed. The results show that the expression of dormancy was temperature dependent, so that the minimum temperature for 100% budburst rose during the induction and dropped during the release of dormancy. These responses may explain previous contradictions between experimental and modelling studies, but that needs to be verified with more extensive experiments, some of which are identified in this study. The results provide further evidence for the concept of gradual change in bud dormancy. They also suggest that global change studies modelling budburst phenology should address the changing expression of bud dormancy.  相似文献   

6.
We investigated interrelations of dormancy and freezing tolerance and the role of endogenous abscisic acid (ABA) in the development of silver birch (Betula pendula Roth) ecotypes in controlled environments. Short-day treatment induced growth cessation, bud set and dormancy development, as well as initiation of cold acclimation and an increase in freezing tolerance. Subsequent low temperature and short days (12-h photoperiod) resulted in a significant increase in freezing tolerance, whereas bud dormancy was gradually released. The concentration of ABA increased in response to short days and then remained high, but ABA concentrations fluctuated irregularly when the dormant plants were subsequently exposed to low temperature during short days. Although there was a parallel development of freezing tolerance and bud dormancy in response to short days, subsequent exposure to low temperature had opposite effects on these processes, enhancing freezing tolerance and releasing dormancy. Compared with the southern ecotype, the northern ecotype was more responsive to short days and low temperature, exhibiting earlier initiation of cold acclimation, growth cessation and an increase in ABA concentrations in short days, and higher freezing tolerance, faster dormancy release and greater alteration in ABA concentrations when subsequently exposed to low temperature during short days. The rates and extent of the increases in ABA concentration may be related to increases in freezing tolerance and dormancy development during short days, whereas the extent of the fluctuations in ABA concentration may play an important role in enhancing freezing tolerance and releasing dormancy during a subsequent exposure to low temperature during short days.  相似文献   

7.
Detailed knowledge of temperature effects on the timing of dormancy development and bud burst will help evaluate the impacts of climate change on forest trees. We tested the effects of temperature applied during short-day treatment, duration of short-day treatment, duration of chilling and light regime applied during forcing on the timing of bud burst in 1- and 2-year-old seedlings of nine provenances of Norway spruce (Picea abies (L.) Karst.). High temperature during dormancy induction, little or no chilling and low temperature during forcing all delayed dormancy release but did not prevent bud burst or growth onset provided the seedlings were forced under long-day conditions. Without chilling, bud burst occurred in about 20% of seedlings kept in short days at 12 degrees C, indicating that young Norway spruce seedlings do not exhibit true bud dormancy. Chilling hastened bud burst and removed the long photoperiod requirement, but the effect of high temperature applied during dormancy induction was observed even after prolonged chilling. Extension of the short-day treatment from 4 to 8 or 12 weeks hastened bud burst. The effect of treatments applied during dormancy development was larger than that of provenance; in some cases no provenance effect was detected, but in 1-year-old seedlings, time to bud burst decreased linearly with increasing latitude of origin. Differences among provenances were complicated by different responses of some origins to light conditions under long-day forcing. In conclusion, timing of bud burst in Norway spruce seedlings is significantly affected by temperature during bud set, and these effects are modified by chilling and environmental conditions during forcing.  相似文献   

8.
We studied the variation in critical night length for bud set in two photoperiodic ecotypes (two latitudinally distant stands) of silver birch (Betula pendula Roth) in three phytotron experiments. Seeds from 21 open-pollinated mother trees in a southern (Tuusula, 60 degrees N) and a northern (Kittil?, 67 degrees N) Finnish stand were germinated and grown for 4 weeks in a 24-h photoperiod in a greenhouse and then moved to different night length treatments at 18 degrees C for 4 to 6 weeks. Night lengths from 5 to 8.5 h were used for southern origin seedlings and from 1 to 4.5 h for northern origin seedlings. At the end of the treatments, apical bud set was observed and the percentage of seedlings with bud set calculated for each treatment and tree progeny. The critical night lengths (CNL) for 50% bud set were determined separately for seedlings from each mother tree by regression analysis. In both ecotypes, the mean percentage of seedlings with bud set was lowest for the shortest night lengths and increased rapidly as night lengths increased. Mean CNL with its 95% confidence interval for the southern and northern ecotypes was 6.3 +/- 0.2 and 3.1 +/- 0.3 h, respectively. The CNL of the two ecotypes differed significantly in three experiments. Within-ecotype variance of the CNL was significantly higher in the northern ecotype (0.484) than in the southern ecotype (0.150). Significant differences in CNL were detected between individual mother trees of the southern ecotype, but not between mother trees of the northern ecotype. The ranking of individual mother trees, based on CNL, differed in the three experiments.  相似文献   

9.
The chilling requirement of rest completion and the high temperature requirement of growth initiation were determined in three origins of silver birch (Betula pendula Roth.) seedlings and five origins of Scots pine (Pinus sylvestris L.) seedlings. In both the pine and birch the chilling requirement was highest in maritime Scottish origins and lowest in the most continental Finnish and Russian origins. The requirement for southern mountainous Spanish and Bulgarian pine origins was in between. In terms of the high temperature requirement, there were no clear differences between origins. These results suggest that owing to their high chilling requirement, which prevents the beginning of growth and the loss of frost hardiness during the frost‐exposed season, origins from a maritime climate could be the most tolerant under climatic warming.  相似文献   

10.
Dormancy induction in temperate deciduous plants is thought to be regulated by short photoperiods, but low temperature has been shown to eliminate the short photoperiod requirement in northern ecotypes. An F2 population (191 plants) red osier dogwood (Cornus sericea L.) derived from a polycross of an F1 population produced from reciprocal crosses of the parental clonal ecotypes, Northwest Territories (NWT, 62 degrees N) and Utah (42 degrees N), was examined to identify molecular markers of temperature-induced endodormancy. Dormancy induction curves were generated for each individual in the F2 population and a standard point prior to vegetative maturity (i-VM) was inferred from the change in slope of the dormancy acquisition curve. Under Saskatoon, Saskatchewan field conditions (52 degrees N), the NWT ecotype entered i-VM on average 5-6 weeks before the Utah ecotype. Two sub-populations of the F2 population were distinguishable based on VM acquisition on exposure to low temperature but not to short photoperiods. A sequence characterized amplified region (SCAR) marker was developed that correctly (> 92%) identified individual plants within the F2 subpopulation that were responsive to low-temperature induction of VM. Timing of bud break was strongly associated with the timing of VM in the geographical ecotypes but not in the F2 population, indicating that these are separate traits under genetic control.  相似文献   

11.
Abstract

One of the main disadvantages of wood is hygroscopicity resulting from its polar character. The sorption–desorption of water causes unwanted swelling and shrinkage in wood. Thermal modification substantially reduces this inconvenient feature. Unfortunately, the same chemical changes that reduce water sorption alter the polar character of the material and result in poorer wetting of thermally treated wood by waterborne adhesives. Gluability of thermally modified beech (Fagus silvatica L.) and birch (Betula pubescens Ehrh.) wood with two commercial amino resins, melamine–urea–formaldehyde (MUF) and melamine–formaldehyde (MF), and a two-component polyurethane (PUR) adhesive was investigated. Both wood species were modified according to two temperature regimes: 160°C and 190°C. Shear strengths of the joints were then determined according to EN 205:2003 standard. The results showed that thermally modified beech and birch wood can be effectively glued not only with commercially available PUR adhesives, but also with aqueous MF and MUF resins. The resultant shear strengths of the joints were limited by the strength of the thermally modified substrate.  相似文献   

12.
Two‐year‐old seedlings of Betula pendula Roth of three provenances were cut to stump heights of 0 and 10 cm. The birch stumps were exposed to different light levels (25–400 μEm?2s?1) and temperatures (6–24°C) for 100 days in climate chambers. Birches were also cut down to seven stump heights (0, 2, 5, 10, 15, 20 and 25 cm) and exposed to light intensity 25 and 200 μEm?2s?1 at 12/6°C for 100 days in climate chambers. In the third experiment 10 cm stumps of birch were exposed to different light intensities (10–400 μEm?2s?1) for 30 days in a greenhouse at 20°C. Starch content in root systems was analyzed before and after treatment. Ten stumps per treatment were used in the experiments except the third experiment where 15 stumps were used. The number of sprouting stumps was correlated with light intensity and temperature. None of the stumps exposed to 6 or 9°C produced suckers. At stump height 0 cm fewer sprouting stumps were produced than at 10 cm. The mean height of suckers was higher the higher the temperature both on 0 and 10 cm stumps. There were differences between provenances in height growth. The number of suckers per sprouting stump was not related to temperature or light intensity. Starch content in root systems of 10 cm high stumps was 4.0% compared with 14.7% in root systems of non‐stumped birch plants after 30 days in the greenhouse. Starch content decreased from 4.0 to 3.0% with decreasing light intensity (400–10 μEm?2S?1). The number of suckers and their mean height were correlated with starch content depending on light intensity.  相似文献   

13.
Eleven paper birch (Betula papyrifera Marsh.) provenances from a single geographic region in northern Idaho and four geographic regions in British Columbia (BC) were studied to determine whether morphometric variability was due to species' genetics, growing environment, or their interaction. Seedlings were grown at three nurseries in BC and Idaho and planted in a randomised single-tree interlocking block design at Skimikin (50°47′) and Red Rock (53°45′) common gardens in BC. Geographic variation in birch height growth was regulated by genetics and a complex interaction with environmental factors. Growth does not follow latitudinal, longitudinal or elevational clines although provenances at the southern garden showed better height growth compared to the northern garden. Greater percentages of seedling mortality were observed at the northern garden compared to provenances planted at the southern garden. Birch height growth was significantly influenced by nursery displacement effects up to four years after establishment. The safe range of southward seed-transfer distance may be as much as 5°, and beyond this limit a detrimental effect likely occurs. Collectively, these results suggest that a provenance best suited to one environment might not be the best for another environment. However, these findings will be useful in understanding the genecology of paper birch when establishing operational seed-transfer guidelines in BC.  相似文献   

14.
Two-year-old Fagus sylvatica L. seedlings were subjected to natural winter chilling or were overwintered in a heated greenhouse. Plants were then grown in controlled environment chambers with photoperiods of 9 or 13 h. Renewal of bud growth was found to be mainly determined by winter chilling. There was a slight interaction between chilling and photoperiod. Sprouting of apical buds took two to three times as long in unchilled plants as in chilled plants. Shoot elongation was influenced by chilling and was also greater in the 13-h photoperiod than in the 9-h photoperiod, but this may have been due at least in part to the higher irradiance. Chilling resulted in rapid dormancy loss and changed the growth pattern from basitonal to acrotonal.  相似文献   

15.
First‐year seedlings of five latitudinal populations of Acer platanoides were subjected to decreasing photoperiod treatment under three different temperature regimes. The depth of the induced dormancy was quantified as the number of days to bud burst (DBB) under defined conditions favourable to growth. The results suggested a close relationship between autumn temperature and the strength of the induced dormancy, with high temperatures combined with short days leading to a deeper stage of dormancy. Northern and continental populations generally had bud burst earlier than southern. The results are discussed in relation to hypotheses for dormancy induction and release.  相似文献   

16.
Bud development of boreal trees in spring, once initiated, is driven by ambient air temperature, but the mechanism triggering bud development remains unclear. We determined if some aspect of the diurnal or seasonal light regime influences initiation of bud burst once the chilling requirement is met. We grew 3-year-old birch plantlets cloned from a mature tree of boreal origin in light conditions realistically simulating the lengthening days of spring at 60 degrees N. To emulate the reduction in red to far-red light (R:FR) ratio between daylight and twilight, one group of plantlets was subjected to reduced R:FR ratio in the morning and evening in addition to progressively lengthening days, whereas the other group was subjected to the same R:FR ratio throughout the day. The reduced R:FR ratio of twilight advanced bud burst by 4 days compared with the reference group (P = 0.04). To assess the interplay between the fulfillment of the chilling requirement and the subsequent response to warming, we fitted a thermal time model to the data with separate parameterizations for the starting dates of heat sum accumulation in each treatment. Least-squares fitting suggested that bud development started in light regimes corresponding to late March, almost two months after the chilling requirement for dormancy release was satisfied. Therefore, shortening night length or increasing day length, or both, appears to be the cue enabling bud development in spring, with twilight quality having an effect on the photoperiodic response. If twilight alone were the cue, the difference in bud burst dates between the experimental groups would have been greater than 4 days. The result gives experimental support for the use of thermal-time models in phenological modeling.  相似文献   

17.
In contrast to most temperate woody species, apple and pear and some other woody species of the Rosaceae family are insensitive to photoperiod, and no alternative environmental seasonal signal is known to control their dormancy. We studied growth and dormancy induction in micropropagated plants of four apple (Malus pumila Mill.) and one pear (Pyrus communis L.) commercial rootstock cultivars in controlled environments. The results confirm that growth cessation and dormancy induction in apple and pear are not influenced by photoperiod, and demonstrate that low temperature (< 12 degrees C) consistently induces both processes, regardless of photoperiodic conditions. Successive stages of the autumn syndrome (growth cessation, formation of bud scales and winter buds, leaf senescence and abscission, and dormancy induction) occurred in response to low temperature. Long days increased internode length at higher temperatures, but had no significant effect on leaf production in any of the cultivars. Chilling at 6 or 9 degrees C for at least 6 weeks (about 1000 h) was required for dormancy release and growth resumption, whereas treatment at 12 degrees C was marginally effective, even after 14 weeks of exposure. We are thus faced with the paradox that the same low temperature conditions that induce dormancy are also required for dormancy release in these species.  相似文献   

18.
We tested three theories predicting the timing of bud burst in mature birch (Betula pendula Roth) trees utilizing a 60-year phenological time series together with meteorological temperature observations. Predictions of the timing of bud burst based on light conditions in addition to temperature were more accurate than predictions based on dormancy development and temperature (prediction standard error of 2.4 days versus 4.3 days). The signal from light conditions, represented by fixed calendar date, determined the start of bud ontogenesis rather than dormancy release. We suggest that models developed to predict the timing of bud burst be utilized in the analysis of plant responses to climate change and of climate change itself.  相似文献   

19.
We examined foliar endophyte frequencies in two native (Betula pendula and Betula pubescens) and three exotic (Betula ermanii, Betula platyphylla and Betula resinifera) birch species and their hybrids in Punkaharju, Finland. The most frequently isolated endophytic fungi in the experimental trees were Fusicladium betulae and Gnomonia setacea making up 80–90% of all endophyte infections. Total endophyte infection levels varied from 0.5 colony forming units (CFU)/cm2 in B. platyphylla to 8.6 CFU/cm2 in B. pubescens that had highest total infection levels of both examined endophyte species. The resistance of hybrids was generally very close to the more resistant parent (the only exception being Fusicladium in B. platyphylla × B. pendula hybrid) supporting the hypothesis that the resistance of birch hybrids to these fungi is genetically based and caused by dominant inheritance of resistance traits.  相似文献   

20.
The main purpose of these studies was to investigate the adaptation of young seedlings of various seed lots of Picea abies (L.) Karst., P. glauca (Moench) Voss, P. x lutzii Little and P. sitchensis (Bong.) Carr. to northern climatic conditions. Effects of temperature and photoperiod on elongation growth and growth cessation were studied under controlled conditions in a phytotron. In addition, growth and survival of the seedlings outdoors at 69°39’ N lat. were followed for two years. Seed lots of /’. abies originated from northern Norway (66° N lat.), those of the other species were from Alaska (between 57°.and 66° N lat.). The critical photoperiod for budset was 19–20 h for seed lots of P. abies. In general, the critical photoperiod for budset increased with increasing latitude of the seed source, but the results indicated a significantly shorter cirtical photoperiod for seed lots from about 60° N lat., <120 m a.s.l. of P. sitchensis (between 12 and 16 h) than for comparable seed lots of P x lutzii (17–18 h) or P. glauca (18 h). The time course of budset under natural light conditions, both in the phytotron and outdoors, generally followed the pattern predicted from the critical photoperiod. However, in P. glauca the budset occurred earlier than in P. abies although the latter had a longer critical photoperiod. Due to the short critical photoperiod and consequently delayed growth cessation and hardening, all seed lots of P. sitchensis (from 58° to 60° N lat.) were severely damaged during winter. Some damage was also observed in P. x lutzii and in P. abies. The optimum temperature for elongation growth was higher for P. sitchensis than for the other species. In the phytotron experiments, seedlings of P. sitchensis grew best at temperatures between 12 and 21°C, but at 9°C the best growth was obtained in some seed lots of P. abies. After two growth seasons outdoors, all seed lots of P. abies were taller than any seed lot of the other species. Also P. glauca seed lots and one seed lot of P. x lutzii showed good growth, and their growth rhythm seemed to be well adapted to the northern conditions.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号