Growth and Dormancy in Norway Spruce Ecotypes (Picea abies) I. Interaction of Photoperiod and Temperature

Growth and dormancy as affected by photoperiod and temperature have been studied in Norway spruce ecotypes of different latitudinal and altitudinal origin. First-year seedlings were used. In all ecotypes apical growth cessation and terminal bud formation occurred within 2 weeks after exposure to SD at temperatures of 18 to 24°C. At lower temperatures or at near-critical photoperiods the response was delayed. The critical photoperiod for apical growth cessation varied from 21 hours in ecotype Steinkjer, Norway (64°N) to about 15 hours in ecotype Lankowitz, Austria (47°04′N). High-elevation ecotypes also had longer critical pholoperiods than low-elevation ecotypes from the same latitude. A detectable growth depression resulted from as little as 1 or 2 SDs of 10 hours, and with 4 or more SDs apical growth cessation took place. In contrast to the situation in the shoot, root growth was not affected by photoperiod. Accordingly, the top:root ratio is drastically affected by photoperiod. The critical photoperiod for cambial growth was shorter than that for apical growth in all ecotypes and cambial growth cessation was delayed for several weeks compared with cessation of apical growth. A transition to formation of late-wood tracheids with thick walls and narrow lumens took place upon exposure to SD. The photoperiodic effects were significantly modified by temperature, but the critical photoperiods were only slightly changed by temperature in the range of 12 to 24°C. However, a 10-hour “night” at 4°C caused growth cessation in continuous light in four ecotypes tested. Temperature optimum for apical growth under non-limiting photoperiods (24 hours) was 21°C in all ecotypes, but with little difference among 18,21 and 24°C. The Q₁₀ for apical growth was 3.5 in the temperature range 12 to 18°C. The growth potential as determined in 24-hour photoperiods was not significantly different among the various ecotypes except for one northern eco-type which was clearly inferior to the others. However, the growth of ecotype Steinkjer (64°N) was greatly suppressed even by the long midsummer days at 59°40′N, thus demonstrating the misleading impression one gets of the growth potential of northern ecotypes when they are moved southwards.     

A proposed role for the anaerobic pathway during low-temperature sweetening in tubers of Solanum tuberosum

Survival and growth of temperate zone woody plants under changing seasonal conditions is dependent on proper timing of cold acclimation and development of vegetative dormancy, shortening photoperiod being an important primary signal to induce these adaptive responses. To elucidate the physiological basis for climatic adaptation in trees, we have characterized photoperiodic responses in the latitudinal ecotypes of silver birch ( Betula pendula Roth) exposed to gradually shortening photoperiod under controlled conditions. In all ecotypes, shortening photoperiod triggered growth cessation, cold acclimation and dormancy development, that was accompanied by increases in endogenous abscisic acid (ABA) and decreases in indole-3-acetic acid (IAA). There were distinct differences between the ecotypes in the rates and degrees of these responses. The critical photoperiod and the photoperiodic sensitivity for growth cessation varied with latitudinal origin of the ecotype. The northern ecotype had a longer critical photoperiod and a greater photoperiodic sensitivity than the southern ecotype. Compared with the southern ecotypes, the northern ecotype was more responsive to shortening photoperiod, resulting in earlier cold acclimation, dormancy development, increase in ABA content and decrease in IAA content. However, at the termination of the experiment, all the ecotypes had reached approximately the same level of cold hardiness (−12 to −14°C), ABA content (2.1–2.3 µg g⁻¹ FW) and IAA content (17.2–20.3 ng g⁻¹ FW). In all ecotypes, increase in ABA levels preceded development of bud dormancy and maximum cold hardiness. IAA levels decreased more or less parallel with increasing cold hardiness and dormancy, suggesting a role of IAA in the photoperiodic control of growth, cold acclimation and dormancy development in birch.     

The Cessation of Apical Growth in Latitudinal Ecotypes and Ecotype Crosses of Salix pentandra L

Apical growth cessation in seedling progenies of three latitudinalecotypes and ecotype crosses of Salix pentandra L. was investigatedunder controlled growth conditions and out-of-doors. The southernecotype (59° 40' N) was characterized by late growth cessationunder short day conditions, short critical photoperiod for growthcessation, and high light sensitivity; the northern ecotype(69° 39' N) by rapid growth cessation, long critical photoperiod,and low light sensitivity. The geographically intermediate ecotype(64° 28' N) had an intermediate photoperiodic response.The hybrid progenies were, however, closer to the southern thanto the northern parent ecotype indicating a tendency to favourinheritance of southern characters. Fluctuating temperatures(21 °C/9 °C and 18 °C/9 °C) induced growth cessationin the northern ecotype but not in the other ecotypes or ecotypecrosses with the exception of a few plants of the intermediateecotype and of two hybrid progenies. The time course of apicalgrowth cessation in various progenies grown out-of-doors at69° 39' N was similar to that observed under SD conditionsexcept that the differences between the northern ecotype andthe other ecotypes and crosses were greater.     

Effect of photoperiod and temperature on apical growth cessation in two ecotypes of Salix and Betula

Apical growth cessation as affected by photoperiod and temperature has been studied in seedlings of two latitudinal ecotypes of Salix and Betula. The critical photoperiod for apical growth cessation at constant temperatures of 15 and 21°C was about 22 h for a northern (69°C39′N) and about 15–16 h for a southern (59°C40′N) ecotype of Salix pentandra. Fluctuating day/night temperatures (21°C/9°C, 15°C/6°C) induced apical growth cessation in northern ecotypes even at 24–h photoperiod. Disagreements in critical photoperiods found in various studies are discussed.     

Effect of rootstock on photoperiodic control of elongation growth in grafted ecotypes of Salix

Scions of a southern (59° 40'N Lat.) and a northern (69° 39'N Lat.) ecotype of Salix pentandra L. were grafted on clonal rootstocks of the same ecotypes. Effects of photoperiod on elongation growth of the 4 combinations (south/south, south/north, north/south and north/north) were studied in a phytotron at 18° and 15°C. The photoperiodic response was primarily dependent on the ecotype of the scion, but this response was significantly modified by the rootstock. Cessation of apical growth was advanced by a northern clone and delayed by a southern clone as a rootstock. The results indicate that the critical photoperiod for cessation of apical growth could be slightly decreased by a northern and increased by a southern rootstock.     

Cold acclimation in silver birch (Betula pendula). Development of freezing tolerance in different tissues and climatic ecotypes

A number of environmental cues including short day photoperiod (SD) and low temperature (LT) are known to interact in triggering growth cessation, cold acclimation and other adaptive responses in temperate-zone tree species. Proper timing of these responses is particularly important for survival of trees in the boreal and subarctic regions. Therefore, we used a northern tree species, silver birch ( Betula pendula Roth) as an experimental model to investigate the effect of SD and LT on development of freezing tolerance and on levels of endogenous abscisic acid (ABA) in short-term experiments under controlled conditions. We characterized differences in SD and LT-induced cold acclimation between three different climatic ecotypes from southern, central and northern habitats. The results demonstrated that cold acclimation was rapidly triggered by exposing the plants to SD or LT, and that a combination of the different treatments had an additive effect on freezing tolerance. Freezing tolerance induction was not uniform in the different tissues, the buds and leaves developed freezing tolerance more rapidly than the stem, and the young leaves had a higher freezing tolerance than the old leaves. The ability of the leaves to respond to SD and LT and similarity of the bud and leaf responses indicate that birch leaves provide a rapid and convenient system for studies on molecular mechanisms of cold acclimation. Development of freezing tolerance was dependent on the climatic ecotype, the northern ecotype was clearly more responsive to both SD and LT than the two more southern ecotypes. Development of freezing tolerance induced by SD and LT was accompanied by transient changes in ABA levels. These alterations in ABA levels were ecotype-dependent, the northern ecotype reacting more strongly to the environmental cues.     

Apical Growth Cessation and Shoot Tip Abscission in Salix

Time course of apical shoot growth and shoot tip abortion in northern ecotypes (lat. 69°39′N, long. 18°37′E) of Salix pentandra and S. caprea have been investigated. In trees more than 15 years old growing under natural climatic conditions apical growth cessation and shoot tip abortion normally occurred in June-July when the day length still was 24 h. Application of GA₃, in spring to the apex effectively delayed growth cessation and shoot tip abortion. Application of kinetin was without effect. First-year seedlings of both species grew continuously at temperatue of 9 to 24°C in 24 h photoperiod. Short days induced apical growth cessation, but two to four (S. pentandra) or three to five (S. caprea) weeks of 12 h photoperiod were required to stop the elongation growth. The results indicated that the critical photoperiod for apical growth cessation in the used ecotype of S. pentandra was 16 to 18 h at 18°C. Short days had a minor effect only on the formation of apical leaf primordia in small seedlings. Development of axillary buds and radial growth were stimulated by short days when compared with long days. Small seedlings of both species (3 to 8 cm high at the start) formed terminal buds in short days, but in large seedlings (more than about 15 cm high) apical growth cessation was accompanied by shoot tip abortion. Abscisic acid applied to the apex or through a leaf did not induce growth cessation in S. pentandra seedlings grown in continuous light. The growth retardants CCC, B-9 and Phosphon D reduced growth rate under continuous light and induced shoot tip abortion in some plants. The effect of CCC was counteracted by GA₃. Apical growth cessation in short days was significantly delayed by a single GA₁ application.     

Photoperiod and temperature differentially regulate the expression of two dehydrin genes during overwintering of birch (Betula pubescens Ehrh.)

The overwintering of trees in northern areas depends on processes regulated by photoperiod and temperature. To identify the physiological and genetic factors involved in this environmental control, three latitudinal ecotypes of pubescent birch (Betula pubescens Ehrh.) growing in a common garden experiment were used. Each ecotype responded to the shortening of the photoperiod according to its specific critical daylength, resulting in the induction of freezing tolerance and dehydration of buds first in the northern ecotype, followed by the central and southern ecotypes, respectively. By contrast, there was no clear difference in the timing of dormancy release, bud rehydration, and deacclimation in the spring, suggesting that these traits were controlled mainly by temperature. To elucidate the role of dehydrins (DHN) in the overwintering process, two DHN genomic clones were isolated from pubescent birch and expression of the corresponding genes, both in field and under controlled conditions, was characterized. BpuDhn1 was found to encode an Y(n)K(n)-type of basic DHN, while BpuDhn2 encoded an acidic, SK(n)-type of DHN. In field-grown trees the level of BpuDhn1 increased in buds during the autumn, while the level of BpuDhn2 was highest during the coldest winter months. Under controlled conditions BpuDhn1 increased in response to the combined effect of short daylength and low, non-freezing temperatures whereas the expression of BpuDhn2 was mainly controlled by low temperature while photoperiod had less effect on its expression. These results suggest that DHNs participate in the sensitive environmental regulation of the overwintering process in birch.     

Geographic variation in critical photoperiod for diapause induction and its temperature dependence in Hyphantria cunea Drury (Lepidoptera: Arctiidae)

The fall webworm, Hyphantria cunea Drury (Lepidoptera: Arctiidae), was introduced from North America to Japan half a century ago. The critical photoperiod for diapause induction and its temperature dependence, as defined by the difference in the critical photoperiod between 20 and 25°C, were investigated in order to understand the mechanisms behind a shift from bi- to trivoltine life cycles. The critical photoperiod for diapause induction was shorter in the southern trivoltine populations than in the northern bivoltine populations, and this was more marked at 25°C than at 20°C. Although the critical photoperiod showed a positive correlation with the original latitude, the correlation was relatively low at both temperatures. Conversely, temperature dependence of the critical photoperiod for diapause induction correlated negatively with the original latitude. The trivoltine populations showed greater temperature sensitivity than the bivoltine populations. These results suggest that an increase in temperature sensitivity of the diapause response to photoperiods was involved in the shift to a trivoltine life cycle. The crossing experiments suggested that the photoperiodic control of diapause induction and its temperature dependence are under polygenic control without sex-linkage. Received: 29 October 1996 / Accepted: 26 February 1997     

Ecotype-dependent control of growth,dormancy and freezing tolerance under seasonal changes in <Emphasis Type="Italic">Betula pendula</Emphasis> Roth

Woody plants in the temperate and boreal zone undergo annual cycle of growth and dormancy under seasonal changes. Growth cessation and dormancy induction in autumn are prerequisites for the development of substantial cold hardiness in winter. During evolution, woody plants have developed different ecotypes that are closely adapted to the local climatic conditions. In this study, we employed distinct photoperiodic ecotypes of silver birch (Betula pendula Roth) to elucidate differences in these adaptive responses under seasonal changes. In all ecotypes, short day photoperiod (SD) initiated growth cessation and dormancy development, and induced cold acclimation. Subsequent low temperature (LT) exposure significantly enhanced freezing tolerance but removed bud dormancy. Our results suggested that dormancy and freezing tolerance might partially overlap under SD, but these two processes were regulated by different mechanisms and pathways under LT. Endogenous abscisic acid (ABA) levels were also altered under seasonal changes; the ABA level was low during the growing season, then increased in autumn, and decreased in winter. Compared with the southern ecotype, the northern ecotype was more responsive to seasonal changes, resulting in earlier growth cessation, cold acclimation and dormancy development in autumn, higher freezing tolerance and faster dormancy release in winter, and earlier bud flush and growth initiation in spring. In addition, although there was no significant ecotypic difference in ABA level during growing season, the rates and degrees of ABA alterations were different between the ecotypes in autumn and winter, and could be related to ecotypic differences in dormancy and freezing tolerance.     

The Initiation and Growth of Axillary Bud Primordia in Relation to Flowering in Trifolium repens L.

The initiation and growth of axillary bud primordia in relationto the growth of their subtending leaves was observed at theapices of three clones (A. B. and C) of white clover grown invarious combinations of photoperiod and temperature. ClonesA, B, and C flower in response to low temperatures, and clonesA and C, but not B, in response to a transfer from short tolong photoperiods at higher temperatures. The rate of growth of buds and leaves from node to node waslittle influenced by the various treatments imposed, but theinitiation of axillary bud primordia relative to the apicaldome was stimulated in conditions conducive to flowering. The number of budless leaf primordia at the apex ranged froma maximum average of 2.25 at 20° C. to approximately o.8oat 10° C. in all three clones. At the higher temperatures,runners possessed 2.06 budless nodes in short days but only1.12 in long days in clones A and C. In clone B, daylength didnot influence bud initiation at the higher temperature. The results provide evidence of the homology between vegetativeand repro-ductive axillary bud primordia. It is suggested thatflowering is brought about by the removal of an inhibition withinthe apex which leads to the precocious initiation of axillarybud primordia. Following the initiation of axillary bud primordia, the resultsshow their growth to be uninhibited for 6-7 plastochrons. Rapidinflorescence development occurs during this phase. Apical dominancehas no apparent influence on vegetative axillary buds untilthe onset of rapid petiole elongation in their subtending leaves.     

The Control of Autumn Senescence in European Aspen

The initiation, progression, and natural variation of autumn senescence in European aspen (Populus tremula) was investigated by monitoring chlorophyll degradation in (1) trees growing in natural stands and (2) cloned trees growing in a greenhouse under various light regimes. The main trigger for the initiation of autumn senescence in aspen is the shortening photoperiod, but there was a large degree of variation in the onset of senescence, both within local populations and among trees originating from different populations, where it correlated with the latitude of their respective origins. The variation for onset of senescence with a population was much larger than the variation of bud set. Once started, autumn senescence was accelerated by low temperature and longer nights, and clones that started to senescence late had a faster senescence. Bud set and autumn senescence appeared to be under the control of two independent critical photoperiods, but senescence could not be initiated until a certain time after bud set, suggesting that bud set and growth arrest are important for the trees to acquire competence to respond to the photoperiodic trigger to undergo autumn senescence. A timetable of events related to bud set and autumn senescence is presented.     

Genetic basis of photoperiodic control of summer and winter diapause in geographic ecotypes of the rice stem maggot, Chlorops oryzae

Chlorops oryzae Matsumura (Diptera: Chloropidae) is bivoltine in northern Japan but trivoltine in the southern part of the country. Larvae of the bivoltine strain (Akita, 39° N) develop without delay under L14:D10 but enter summer diapause in the mature larval stage under L15:D9. In contrast, larvae of the trivoltine strain (Aichi, 35° N) develop quickly under L15:D9 but enter summer diapause under L14:D10. The genetic basis of their different summer-diapause behavior was analyzed by reciprocal crossing between the two ecotypes and backcrossing to the hybrids. Although a polygenic system seems to be involved, there is a single gene on the X-chromosome exerting a major effect on summer diapause. The northern bivoltine ecotype has a longer critical photoperiod for the induction of winter diapause in the first larval stage and remains in diapause longer than the southern trivoltine ecotype. The differences in the critical photoperiod and the winter diapause duration between the two ecotypes seem to be controlled by a polygenic system but again a sex-linked or closely linked gene (or genes) plays a major role. The two geographic ecotypes differ significantly in summer- and winter-diapause traits, both of which are characterized by sex-linked inheritance. Despite this, no apparent sterility or inviability in hybrids between the ecotypes occurs.     

A Norway spruce FLOWERING LOCUS T homolog is implicated in control of growth rhythm in conifers

Growth in perennial plants possesses an annual cycle of active growth and dormancy that is controlled by environmental factors, mainly photoperiod and temperature. In conifers and other nonangiosperm species, the molecular mechanisms behind these responses are currently unknown. In Norway spruce (Picea abies L. Karst.) seedlings, growth cessation and bud set are induced by short days and plants from southern latitudes require at least 7 to 10 h of darkness, whereas plants from northern latitudes need only 2 to 3 h of darkness. Bud burst, on the other hand, is almost exclusively controlled by temperature. To test the possible role of Norway spruce FLOWERING LOCUS T (FT)-like genes in growth rhythm, we have studied expression patterns of four Norway spruce FT family genes in two populations with a divergent bud set response under various photoperiodic conditions. Our data show a significant and tight correlation between growth rhythm (both bud set and bud burst), and expression pattern of one of the four Norway spruce phosphatidylethanolamine-binding protein gene family members (PaFT4) over a variety of experimental conditions. This study strongly suggests that one Norway spruce homolog to the FT gene, which controls flowering in angiosperms, is also a key integrator of photoperiodic and thermal signals in the control of growth rhythms in gymnosperms. The data also indicate that the divergent adaptive bud set responses of northern and southern Norway spruce populations, both to photoperiod and light quality, are mediated through PaFT4. These results provide a major advance in our understanding of the molecular control of a major adaptive trait in conifers and a tool for further molecular studies of adaptive variation in plants.     

Flower bud differentiation in Salix pentandra as affected by photoperiod, temperature and growth regulators

Flower bud initiation in seedlings and vegetatively propagated plants of Salix pentandra from different locations has been studied under controlled conditions. In mature plants flower bud formation was induced by 2-chloroethyltrimethylammoniumchloride (CCC) and by short day treatment. The effect of CCC was antagonized by GA₃. The critical photoperiod for flower bud formation was about 18 h for a southern clone (from 49°48'N), but cuttings of a northern ecotype (from 69°39'N) formed flower buds even at 24 h photoperiod. Generally, flower bud formation occurred simultaneously with apical growth cessation. However, apical growth cessation was not a prerequisite for floral initiation and flower buds were also found in elongating plants. Seedlings up to 60 days old did not form flower buds in growth chamber studies. The length of the juvenile phase has not been studied in detail, but cuttings taken from seedlings approximately 20 cm high and 60 days old were able to develop flower buds when treated with CCC. A gradual transition from the juvenile to the mature phase was obtained by repeated pruning of seedlings grown at 18°C and 24 h photoperiod.     

Circadian rhythmicity and photoperiodism in the pitcher-plant mosquito: adaptive response to the photic environment or correlated response to the seasonal environment?

Many plants and animals use the length of day or photoperiod to cue their seasonal patterns of development, reproduction, dormancy, and migration. Among temperate arthropods, the median or critical photoperiod increases with latitude or altitude. Concomitantly, in beetles, moths, mites, flies, and mosquitoes, there is a declining expression of a rhythmic, presumably circadian-based, component of photoperiodic response. It has been proposed that the long summer days in the north select for a reduced response to light by the circadian clock, which results in this declining rhythmic expression and, consequently, longer northern critical photoperiods. However, these patterns might also be due to direct, seasonal selection on the critical photoperiod itself, which results in a correlated reduction in the rhythmic component as a result of internal physiological constraints within the organism. Using standard light duration and selection experiments, we show that evolution of photoperiodic time measurement in the mosquito, Wyeomyia smithii, results from the direct response of critical photoperiod to seasonal selection and a correlated response of the rhythmic component of photoperiodic time measurement. We conclude that expression of the circadian clock is necessary neither for the central mechanism of photoperiodic time measurement nor for the adaptive modification of critical photoperiod.     

Flower development in the passion fruit Passiflora edulis requires a photoperiod‐induced systemic graft‐transmissible signal

Different organisms use gradual seasonal changes in photoperiod to correctly time diverse developmental processes, such as transition to flowering in plants. Florigen is a systemic signal formed in leaves exposed to specific environmental cues, mainly photoperiodic, and capable of triggering flower induction in several species. Here we show that in Passiflora edulis, a perennial climbing vine, flower initiation occurs throughout the year; however, without long photoperiods, flower primordia show arrested growth and differentiation at an early stage. Our results support the existence of a positive, systemic, graft‐transmissible signal, produced in mature leaves under LDs, that is required for normal flower development beyond sepal formation. Our results also suggest that Gibberellin acts to inhibit flower development. We provide evidence for genetic variation in the response to short photoperiods. A genotype capable of forming developed flowers under short photoperiods produces a positive graft transmissible signal allowing normal flower development under short days in a cultivar which normally aborts flower development under these conditions. We believe these findings contribute towards discovering the chemical nature of this interesting mobile signal involved in flower development.     

Responses to stepwise photoperiodic changes for the larval diapause of the Indian meal moth Plodia interpunctella

Abstract The Indian meal moth Plodia interpunctella Hübner (Lepidoptera: Pyralidae) diapauses as a last‐instar (fifth) larva. At 30 °C, no larvae enter diapause under any photoperiodic conditions; at 25 °C, the photoperiodic response curve is a long‐day type with a critical length of approximately 13 h light; at 20 °C, diapause is induced moderately even under long days (> 13 h). Cumulative effects of short days or long days on diapause induction are determined by alternate, stepwise and gradually changing regimes of photoperiod at 25 °C. When the larvae are repeatedly exposed to LD 16 : 8 h and LD 12 : 12 h photoperiods every other day, the incidence of diapause is 37%. When the larvae are placed under an LD 16 : 8 h photoperiod for 2 days and then under an LD 12 : 12 h photoperiod for 1 day, it is 38 %. Exposure to an LD 16 : 8 h photoperiod for 1 day and then to an LD 12 : 12 h photoperiod for 2 days induces only 15% diapause. This may indicate that the photoperiodic information is not accumulated in a simple fashion despite the generally accepted hypothesis (i.e. photoperiodic counter). Larvae exposed to an LD 16 : 8 h photoperiod for 5 days after oviposition express a very high incidence of diapause even under short days between an LD 2 : 22 h and LD 12 : 12 h photoperiod. After 10 days exposure to an LD 16 : 8 h photoperiod, however, the short day does not induce diapause strongly. On the other hand, an LD 12 : 12 h photoperiod in the early larval life is highly effective in the induction of diapause. A gradual increase or decrease of photoperiod (2 min day^?1) shows that the direction of photoperiodic change does not affect the diapause determination.     

Role of the Quality of Light in the Photoperiodic Flowering Response in Four Latitudinal Ecotypes of Chenopodium rubrum L.

The effect of the quality of light on the photoperiodic floweringresponse in four latitudinal ecotypes of Chenopodium rubrumwas examined. Two southern ecotypes, Sel-184 (50°10' N)and Sel-194 (34°20' N), displayed an obligate short-dayplant under white (W), red (R) and blue (B) light. Sel-372 (62°46'N),the most northern ecotype, was day-neutral in B and W lightand had an ambiphotoperiodic response in R light. Sel-374 (60°47'N) was an ambiphotoperiodic in B light and had a short-day responsein W and R light. In the B light regimens, the flowering ofSel-374 was modified from a typical ambiphotoperiodic to day-neutralresponse by changing the temperature from 20°C to 12°C. The photopriodic flowering response in the 8–16 hr photoperiodwas suppressed severely by the reducing light intensity from3,000 to 1,500 ergs.cm^–2.sec^–1, but that in continuousillumination was lowered only slightly by decreasing the lightintensity. The ambiphotoperiodic flowering response differedin its reaction to light; flowering in the 8-18 hr photoperiodrequired a high intensity light independent of the quality oflight, and flowering in the 24 hr photoperiod was promoted byB light. We considered the ambiphotoperiodic flowering responseto be a combination of the obligate short-day flowering responseand the flowering response for an extreme long-day condition,which is favored by B light. Therefore, this photoperiodic responseprobably is an intermediate step in the short-day and day-neutralresponses in day-neutralization. (Received December 8, 1980; Accepted February 20, 1981)     

Temperature-driven plasticity in growth cessation and dormancy development in deciduous woody plants: a working hypothesis suggesting how molecular and cellular function is affected by temperature during dormancy induction

The role of temperature during dormancy development is being reconsidered as more research emerges demonstrating that temperature can significantly influence growth cessation and dormancy development in woody plants. However, there are seemingly contradictory responses to warm and low temperature in the literature. This research/review paper aims to address this contradiction. The impact of temperature was examined in four poplar clones and two dogwood ecotypes with contrasting dormancy induction patterns. Under short day (SD) conditions, warm night temperature (WT) strongly accelerated timing of growth cessation leading to greater dormancy development and cold hardiness in poplar hybrids. In contrast, under long day (LD) conditions, low night temperature (LT) can completely bypass the short photoperiod requirement in northern but not southern dogwood ecotypes. These findings are in fact consistent with the literature in which both coniferous and deciduous woody plant species’ growth cessation, bud set or dormancy induction are accelerated by temperature. The contradictions are addressed when photoperiod and ecotypes are taken into account in which the combination of either SD/WT (northern and southern ecotypes) or LD/LT (northern ecotypes only) are separated. Photoperiod insensitive types are driven to growth cessation by LT. Also consistent is the importance of night temperature in regulating these warm and cool temperature responses. However, the physiological basis for these temperature effects remain unclear. Changes in water content, binding and mobility are factors known to be associated with dormancy induction in woody plants. These were measured using non-destructive magnetic resonance micro-imaging (MRMI) in specific regions within lateral buds of poplar under SD/WT dormancing inducing conditions. Under SD/WT, dormancy was associated with restrictions in inter- or intracellular water movement between plant cells that reduces water mobility during dormancy development. Northern ecotypes of dogwood may be more tolerant to photoinhibition under the dormancy inducing LD/LT conditions compared to southern ecotypes. In this paper, we propose the existence of two separate, but temporally connected processes that contribute to dormancy development in some deciduous woody plant: one driven by photoperiod and influenced by moderate temperatures; the other driven by abiotic stresses, such as low temperature in combination with long photoperiods. The molecular changes corresponding to these two related but distinct responses to temperature during dormancy development in woody plants remains an investigative challenge.