Growth Hormone Changes in Chrysanthemum morifolium: Effects of Environmental Factors Controlling Flowering

Simultaneous quantitative analyses have been made of the endogenouslevels of auxin- and gibberellin like substances, growth inhibitors,and auxin-oxidizing enzyme activity in the cold-requiring Chrysanthemummorifolium cv. Sunbeam subjected to different daylength, lightintensity and temperature regimes known to affect flowering.While little hormone or enzyme activity was found in extractsfrom unvernalized plants, a striking rise in auxin-oxidizingenzyme activity occurred rapidly after the end of cold treatment.Increased auxin activity was also recorded shortly after vernalization.At 28 °C both enzyme and auxin activity declined over aperiod of 3–4 weeks; at 20 °C this response was delayed.Gibberellin activity at 28 °C rose steeply about 2 weeksfrom vernalization and declined several weeks later; at 20 °Ca similar response was less marked. Low light intensity treatment,which may have increased endogenous auxin levels, or exogenousauxin application reduced gibberellin-like substance levelsand cause d devernalization.Phosphon D treatment also loweredgibberellin levels and prevented flowering. An extract fromvernalized plants containing gibberellin-like substances intensifiedthe flowering of partially vernalized test plants. Persistenceof high auxin activity in vernalized plants on long days wasassociated with failure to form normal flower buds. Stem elongationrates correlated in general with levels of endogenous auxin-and gibberellin-like substances. Significant amounts of an abscisin-likeinhibitor were found in extracts of flower buds. The mechanismof natural devernalization is discussed in relation to theseobservations.     

Changes in the Pattern of Cell Division in the Shoot and Root Meristems of Lolium perenne during the Transition from Vegetative to Floral Growth

For Lolium perenne cv. Cropper, a system which resulted in 100%flowering comprised 90 short days (SD) at 4 ?C (vernalization)and 30 SD at 18 ?C followed by 8 long days (LD). The mitoticindex and G1 and G2 percentages were measured in the shoot androot apices of plants following 2, 5 or 8 LD and in SD controlssampled at the beginning and end of induction. Identical measurementswere made in plants given 48 SD at 18 ?C followed by 2, 5 or8 LD; plants remained vegetative in response to this treatmentlacking vernalization. Significant increases in both mitoticindex and meristem size occurred in the shoot apex in LD followingthe vernalizing, but not the non-vernalizing, treatment. A clusterof mitoses in the apical dome of the shoot apex was unique tothe vernalized plants given 5 or 8 LD. However, an increasein root meristem size occurred regardless of vernalization,but a significant increase in the mitotic index was limitedto vernalized plants given 5 or 8 LD. Whilst the vernalization-LDtreatment resulted in an increase in the G2 percentage in theshoot apex following 2, 5 or 8 LD, no such alteration was observedin the root meristem. Thus, the changes to the cell cycle whichcorrelated with flowering were increased mitotic indices andG2 percentages in the shoot apex at each sampling time and increasedmitotic indices in the root apex following 5 and 8 LD. Key words: Cell division, flowering, Lolium perenne L.     

Effect of nucleic acid antimetabolites on the vernalization of winter wheat

Excised winter wheat embryos were cold-treated in White's mediumcontaining 2% sucrose for 60 days at 4°C. Embryos couldbe vernalized in medium containing sugar, whereas the additionof 8-azaguanine to the medium at the concentration of 10^–4M inhibited vernalization. (Received May 2, 1975; )     

Vernalization in Lolium temulentum L.: Responses of In Vitro Cultures of Mature and Immature Embryos, Shoot Apices and Callus

Response of vernalization to low temperature (2C) was studiedin a winter-annual form of Lolium temulentum L., using imbibedseeds, excised mature and immature embryos, shoot apical meristemsand callus tissue. Excised embryos, as early as 5 days afteranthesis, and excised shoot apices could be vernalized as effectivelyas imbibed seeds. Cold treatment of developing embryos withinthe ear, however, appeared to have no vernalizing effect. Plantsderived from callus by somatic embryogenesis showed varyingdegrees of vernalization response. The vernalization response in L. temulentum, as in winter annualcereals, appears to be located in the shoot apical meristemand the vernalized condition can be transmitted to new axillarymeristems formed from it. Lolium temulentum L. darnel, vernalization, embryo culture, apical meristem culture, callus culture     

Effects of Temperature, Photoperiod and Seed Vernalization on Flowering in Faba Bean Vicia faba

Factorial combinations of three photoperiods (10, 13 and 16h), two day temperatures (18 and 28 °C) and two night temperatures(5 and 13 °C) were imposed on nodulated plants of six diversegenotypes of faba bean (Vicia faba L.). Plants were grown inpots in growth cabinets from both vernalized (1.5±0.5°C for 30 d) and non-vernalized seeds. The times from sowingto the appearance of first open flowers (f) were recorded. Seedvernalization decreased the subsequent time taken to flowerin almost all genotype x growing environment combinations (theexceptions were plants of the cv. Maris Bead grown in threecooler, short-day regimes). The influence of temperature andphotoperiod on the rate of flowering was quantified, using amodel applied previously to other long-day species of grainlegume in which positive linear relations between both temperatureand photoperiod and the rate of progress towards flowering areassumed to apply. A significant positive linear response ofrate of progress towards flowering to limited ranges of meandiurnal temperature was detected in all six genotypes, but inthree genotypes (Syrian Local Large, Aquadulce and Maris Bead)the 28 °C day temperature reduced the rate of progress towardsflowering - suggesting that the optimum temperature for floweringin these genotypes is below 28 °C. In four genotypes (MarisBead, Giza-4, Aquadulce and BPL 1722) a significant positiveresponse to photoperiod, typical of quantitative long-day plants,was observed only in plants grown from vernalized seeds. Incontrast, plants of the genotype Zeidab Local grown from bothnon-vernalized and vernalized seeds showed the same positiveresponse to photoperiod, whereas plants of the land-race SyrianLocal Large were consistently unresponsive to photoperiod. Theimplications of this range of responses amongst diverse genotypesare discussed in relation to screening germplasm. Vicia faba, faba bean, flowering, photoperiod, temperature, seed vernalization, germplasm screening     

Stimulation of generative development in partly vernalized winter wheat by animal sex hormones

The influence of selected animal steroid sex hormones, on generative development of winter wheat var. Grana was investigated. Wheat plants of this variety necessitate 63-day long vernalization. Mature, isolated embryos of wheat were cultured in vitro on media containing androsterone, androstenedione, estriol, estrone, 17β-estradiol and progesterone in concentrations 10⁻⁵ and 10⁻⁶ M. They were not vernalized or vernalized for 7, 14, 21 and 28 days (5 °C, 8 h photoperiod). Investigated steroids stimulated the generative development of winter wheat by an increasing in the percentage of heading plants and accelerating the heading. The strongest effect was observed when plants were treated with steroids during the suboptimal, 21 and 28 day, vernalization. After 28 days of vernalization, 100 % heading were observed in plants obtained on the media containing androsterone and androstenedione in concentrations 10⁻⁵ and 10⁻⁶ M or estrone, 17β-estradiol and progesterone in concentration 10⁻⁵ M. Control plants showed only 8 % heading. An erratum to this article is available at .     

Environmental Control of Flowering in Barley (Hordeum vulgare). III. Analysis of Potential Vernalization Responses, and Methods of Screening Germplasm for Sensitivity to Photoperiod and Temperature

Three genotypes of barley were subjected to 18 potentially vernalizingpre-treatments, comprising constant temperatures of 1, 5 or9 °C in factorial combination with photoperiods of 8 or16 h d^–1 for 10, 30 or 60 d^–1. These pre-treatedseeds or seedlings, together with non-pre-treated seeds as controls,were then transferred to each of four growing-on regimes, namelyday/night temperatures of 18/5 °C or 24/3 °C in factorialcombination with photoperiods of 11 or 16 h d^–1. The timesfrom sowing to awn emergence were recorded. The warmer growing-onregime (mean 19 °C) was not supra-optimal in long days,but in short days it considerably delayed awn emergence in allthree genotypes. In cv. Athenais there was no specific responseto the potentially vernalizing pre-trcatments: the rate of progresstowards awn emergence could be treated as a linear functionof the integrated responses to temperature and photoperiod actingindependently throughout development. In addition to these responses,cv. Gerbel B and the land-race Arabi Abiad also responded tolow-temperature vernalization and the response became saturatedduring the longer-duration pre-treatments. In Arabi Abiad, therate at which vernalization occurred, and the period requiredto saturate the response, were not greatly influenced by differencein pre-treatment temperature between 1 and 9 °C. In contrast,in Gerbel B the cooler the temperature of pre-treatment thegreater the saturated response to vernalization, the greaterthe effect of each day of pre-treatment, and the shorter theperiod required to saturate the response. Models of the photothennaland vernalization responses were combined in a single entitywhich described the influence of environment on rate of development.Simple germplasm-screening techniques are proposed for genotypecharacterization so that the phenotypic flowering response canbe estimated for any environment Hordeum vulgare L., barley, flowering, phtoperiodism, vernalization, photothennal time, germplasm screening     

Factors affecting plant regeneration from immature inflorescence of two winter wheat cultivars

Inflorescence explants of two winter wheat cultivars, Triticum durum cv. Kızıltan-91 and T. aestivum cv. Bezostaja-01, were used to evaluate the effects of vernalization period of donor plants, callus age and medium composition on regeneration capacity. Donor plants were grown for 7 d and they were exposed to 4 °C for 1, 2, 3, 4, and 5 weeks. The maximum inflorescence formation was observed as 79 % at 4 weeks and 73 % at 5 weeks of vernalization period for Kızıltan-91 and Bezostaja-01, respectively. Among 6 different callus induction and regeneration mediums, I₁-R₁ and I₃-R₃ have to be the best responding mediums for Kızıltan-91 and Bezostaja-01, respectively. In Kızıltan-91, calli induced from donor plants, vernalized for 3 weeks, showed a significantly lower regeneration capacity than counterparts vernalized for 4 and 5 weeks. The highest regeneration capacity of 69 % was obtained from 6-week-old calli produced from 4 weeks vernalized Kızıltan-91 donor plants. In contrast to Kızıltan-91 cultures, the effects of vernalization period and callus age on regeneration capacity were not significant in Bezostaja-01 cultures. The maximum numbers of tillers were obtained from 6-and 15-week-old calli for Bezostaja-01 and Kızıltan-91, respectively. In contrast to vernalization period of donor plants, callus age had no effect on seed number.     

Germination of Tagetes minuta L. I. Temperature Effects

Initial studies have indicated that Tagetes minuta achenes haveboth a temperature and a light requirement for germination.Temperatures tested were 10, 20, 25, 30 and 35 °C. Germinationwas optimal at 25 °C under white light conditions. Underthese conditions 100 per cent of achenes germinated within 7days of imbibition. There was no germination at 10 or 35 °Ceither in the light or in the dark. Achenes imbibed and incubatedat 35 °C for 4 days showed no visible signs of germinationbut on transfer to 25 °C, 100 per cent of these achenesgerminated within 24 h. Furthermore, achenes given this hightemperature (35 °C) treatment could be dried at 25 °C,re-imbibed at 25 °C and again 100 per cent of achenes germinatedwithin 24 h of re-imbibition. This rapid germination responsefollowing removal from the high temperature regime could alsobe induced by transfer to temperatures of 20 °C or 20 °C(16 h) alternating with 10 °C (8 h). Tagetes minuta L., weed seeds, germination, temperature, light     

Photothermal Time for Flowering in Faba Bean (Vicia faba) and the Analysis of Potential Vernalization Responses

One cultivar and one land-race of faba bean were subjected to18 potentially vernalizing pre-treatments (constant temperaturesof 1, 5 or 9 °C factorially combined with photoperiods of8 or 16 h d^–1 for 10, 30 or 60 d), and then transferredinto four different growing regimes (‘day’/‘night’temperatures of 18/5 °C or 24/13 °C factorially combinedwith photoperiods of 11 or 16 h d–1). Control plants weregrown entirely in the latter four regimes. The times from sowingto appearance of first open flowers were recorded for all plants.Control plants of the land-race Zeidab Local flowered soonerin long days and in the warmer regime. Pre-treatment reducedthe subsequent time to flower in the four growing-on regimesbut most of the variation in the total time to first flowerfor the pre-treated plants was accounted for by differencesin the combined photothermal time accumulated in the two successiveenvironments - which was predicted by a simple photothermalmodel. Thus, there was neither a specific low-temperature nora short-day vernalization response in this accession. Similarly,no true low-temperature or short-day vernalization responsewas detected in the cv. Maris Bead. However, this UK cultivarflowered later than predicted in the 24/13 °C regime, indicatingthat the 24 °C ‘day’ temperature was supraoptimal.Delays to flowering at 24/13 °C were, however, less evidentwhen plants were grown in long days or following prolonged (30–60d) pre-treatments at cool temperatures. Viciafaba faba, bean, flowering, photoperiodism, vernalization, photothermal time, screening germplasm.     

Primary and Secondary Induction Requirements for Flowering of Contrasting European Varieties of Lolium perenne

The flowering requirements of six European varieties of Loliumperenne L. were studied in controlled environments. In experimentson primary induction, flowering was recorded after transferto long days (LD) in a greenhouse at 12–24°C. In experimentson secondary induction, primary induction was first accomplishedat 6°C/10 h daylength for 12 weeks. When evaluated by the50% heading criterion, the requirement for duration of primaryinduction at 6°C/8 h daylength was <3 weeks in Mediterranean,5–6 weeks in Central European and 7–8 weeks in Scandinavianvarieties. While ‘Veyo’ (Italy) flowered profuselyregardless of temperature or daylength during primary induction,critical temperatures for primary induction in SD and LD were15 and 11°C in ‘Baca’ (Czech Republic) and 11and 7°C in ‘Falster’ (Denmark). The criticalphotoperiod for secondary induction at 15°C ranged from12 h in ‘Veyo’ and 14 h in ‘Baca’ to16.5 h in ‘Falster’ and 17.5 in ‘Kleppe’(Norway). The critical number of LD cycles varied correspondingly.While the Central and North European varieties required fewerLD cycles for 50% heading at 18 than at 12°C, ‘Veyo’showed the opposite response. It is concluded that the requirementsfor both primary and secondary induction of Lolium perenne increasewith increasing latitude of origin of the germplasm. In oneexperiment, 39–87% of the inflorescences came from tillersthat were not visible on transfer from primary to secondaryinduction, thus it is also concluded that there is no juvenilestage in tillers of Lolium perenne. Copyright 2000 Annals ofBotany Company Daylength, flowering, juvenility, perennial ryegrass (Lolium perenne L.), primary induction, secondary induction, temperature, varieties, vernalization     

Effects of Interactions Between Low and High Temperature Treatments on Flowering of Spring Rape (Brassica napusvar.annua)

Exposure to high temperature (30 °C) before or after exposureto low temperature (0, 4 or 8 weeks at 4 °C) consistentlyincreased the number of leaf nodes at flowering and delayedflowering in a range of genotypes of spring rape(Brassica napusvar.annuaL.).Four days of prior exposure to high temperature had more effectthan 2 d, and the effect of subsequent exposure to high temperaturewas maximized when exposure commenced 1 week after the end ofthe low-temperature treatment. In genotypes that showed a vernalizationresponse (i.e. in which the number of leaf nodes at floweringwas reduced or flowering was advanced by low temperature), thisresponse was reduced or eliminated by either prior high-temperaturetreatment (antivernalization) or subsequent high-temperaturetreatment (devernalization). A biochemical model to accountfor these effects is proposed.Copyright 1998 Annals of BotanyCompany Brassica napusvar.annua, spring rape, antivernalization, devernalization, vernalization     

Flowering in Pisum: Kinetics of the Vernalization Response in Genotype If e Sn Hr

Previous work has shown that vernalization acts at two sites,one in the cotyledons and one in the shoot, in young plantsof genotype Ife Sn Hr. During the present study the size ofthe vernalization responses in both the cotyledons and shootincreased as the temperature was lowered from 17 to 3 °C.This occurred regardless of whether the treatment was givenfor the same chronological period of time or for the same physiologicalperiod of time. Vernalization treatment was effective from thetime the seeds were developing in the pods on the maternal plantuntil at least 20 leaves were expanded and became graduallymore effective as the length of the treatment was increasedfrom 2 to 5 weeks. High pre– or post–vernalizationtemperatures can reduce the cotyledon effect and to a lesserextent the shoot effect of vernalization. Devernalization occurredto a larger extent in low light intensities and darkness thanin high light intensities. No stabilization of the vernalizationeffects in the cotyledons or shoot appeared to occur at normalgrowing temperatures (15–25 °C). These results arediscussed in terms of the previously hypothesized mechanismsfor the cotyledon and shoot effects of vernalization. Pisum sativum, flowering, vernalization     

Factors controlling Flowering in the Chrysanthemum: V. DE-VERNALIZATION IN RELATION TO HIGH TEMPERATURE AND LOW LIGHT INTENSITY TREATMENTS

Experiments are described which indicate that the annual vernalizationrequirement of the basal shoots of the Chrysanthemum is dueto annual devernalization of these shoots as the main axis growsup and flowers. Plants sprayed with varying concentrations ofmaleic hydrazide were arrested in their growth for considerableperiods, but this enforced ‘dormancy’ did not affecttheir vernalization status. This makes it appear unlikely thatmere suppression of growth through apical dominance of the mainshoot is the cause of this de vernalization of basal shoots.Fully or partly vernalized plants heated to 40° C. for upto 30 hours did not become dc-vernalized. Heat treatment at35° C. for as long as 30 days also failed to achieve completedc-vernalization, but here flowering was delayed by periodsequivalent to the time spent at high temperature. However, atthe end of the heat treatment progress towards flowering wasresumed at the normal rate. Complete dc-vernalization can bebrought about by prolonged exposure to low intensity illumination.This treatment appears to be effective right up to the stagewhen the first morphological changes leading to inflorescenceformation take place. These results are discussed in relationto similar experiments on the de-vernalization of rye and Hyoscyamusniger.     

Contents of polyamines during vernalization in wheat and the effect of zearalenone

The contents of endogenous free and conjugated polyamines, putrescine (Put) and spermidine (Spd), were determined during 9 week of vernalization (at 5 °C) in winter wheat seedlings cultivated on Murashige and Skoog media without (MS0) and with 2 mg dm⁻³ zearalenone (MSZEN). At the 4^th week of chilling treatment, which is sufficient to induce generative development in 30 % of plants, the marked increase in free and conjugated forms of Put and free Spd were observed. The presence of ZEN in medium significantly accelerated the vernalization. About 20 % of plants treated with ZEN flowered already after 2 weeks and 40 % after 3 weeks of chilling. Significantly higher content of free Put was determined in roots grown on MSZEN compared with MS0 during the first 5 weeks of vernalization with maximum at the 4^th week. After germination, a marked decrease in free Spd content was observed both in plants grown on MS0 and MSZEN. Application of ZEN significantly slowed down the Spd decline in leaves and roots during the first and second week of vernalization. The content of Spd and its conjugates decreased in vernalized plants after 1 week of cultivation at 20 °C.     

The Influence of Donor Plant Genotype and Environment on Production of Multicellular Microspores in Cultured Anthers of Brassica napus ssp. oleifera

Studies of the effects of genotype and pre-flowering environmentalconditions on the production of multicellular microspores wereundertaken th four highly inbred lines of Brassica napus sap.oleifera. These lines were first grown in shaded and unshadedenvironments at 20/15°C arid unshaded at 30/25°C ina daylight phytotron. Buds were harvested from half the plantswhen first visible in the rosette and later from the remainingplants at the time when the first flower opened. The frequencyof microspores at a specific stage of development varied widelywithin a relatively narrow range of bud lengths. Uninucleatemicrospores were not detected in anthers from buds less than1·5 m or greater than 3·0mm long, but were generallypresent in frequencies of greater than 50 per cent in anthersfrom buds which were between 2·0 and 2·5 mm inlength. However, the bud length at which the highest frequencyof uninucleate microspores was detected varied significantlybetween genotypes and between the environments in which theywere grown. Examination of the remaining anthers from each budafter a period in culture revealed that the proportion of microsporesdeveloping into multicellular units varied greatly with budlength, an increase in frequency of multicellular microsporesbeing associated with an increase in the frequency of uninucleatemicrospores in the uncultured anther. Genotypes differed, however,in respect of the relationship between uninucleate microsporefrequency and production of multicellular units. Although thefrequency of multicellular units was as high as 57 percent,further development was limited and the number of embryoldsformed was low in all cases (<10 per cent). The frequency of multicellular units in pollen samples frombuds of a length in which uninucleate microspore frequency washigh varied significantly with genotype, temperature and lightconditions under which donor plants were grown, and the stageof inflorescence development at which buds were removed. Underconditions most conducive to multicellular unit formation (20/15°C,unshaded), the maximum frequency of multicellular units foreach genotype in buds from young inflorescences ranged from11·5 to 56·5 per cent. Shading or exposure tothe higher temperature was associated with a marked reductionin production of multicellular units. Higher frequencies ofmulticellular units were generally detected in microspore samplesfrom younger inflorescences irrespective of genotype or environment. Two of the four inbred lines were selected for a second experimentin which responses to vernalization and photoperiod durationwere monitored. There was a significant reduction in the numberof leaf nodes formed prior to floral initiation in both genotypesfollowing exposure to vernalization and/or a longer photoperiod,the response to photoperiod being more pronounced. Exposureto 4 weeks vernalization was accompanied by a significant increasein the frequency of multicellular units in both genotypes, thefrequency being double that in unvernalized plants under thelonger photoperiod. By contrast, genotypes differed sharplyin their response to photoperiod. In TB 20, the frequency ofmulticellular units was unaffected by an increase in day lengthirrespective of whether seed had been vernalized or not. Onthe other hand, in TB 42 the frequency of multicellular unitswas substantially greater in the 24 h day than in the 12 h day,being 27·3 per cent vs 13·0 per cent in the caseof unvernalized plants and 66·7 per cent vs 18·2per cent in the case of vernalized plants. Brassica napus, anther culture, pollen embryogenesis, genotype-environment interaction     

Dormancy in Dioscorea: Range, Duration and Timing of High-Temperature Treatment in Germination Inhibition of D. tokoro Seeds

The effects of temperature on induction and release of high-temperatureinhibition in seed germination of Dioscorea tokoro Makino, amonocotyledonous summer perennial of the temperate zone of EastAsia, were investigated. Germination was increasingly inhibitedwith elevation of temperature over 23°C and lengtheningof its duration. The low temperature limit for germination inhibitiondecreased with lengthening of the duration of high temperature.The most sensitive phase for high temperature was 1–2days after the start of imbibition at 20°C. The germination inhibition by high temperature was reversedby chilling at 5°C, which is the optimum temperature forbreaking the natural dormancy (primary dormancy) of this seed.This showed that the high-temperature inhibition of germinationdoes not cause mortal damage but only secondary dormancy (induceddormancy). Seeds from a cold climate (Miyagi Pref.) responded rather quicklyto both high temperature and chilling compared to seeds froma warm climate (Kagoshima Pref.). The responsiveness to hightemperature and chilling of D. tokoro seed may affect the germinationtime under natural conditions. (Received October 22, 1982; Accepted January 14, 1983)     

Flowering Responses of Contrasting Ecotypes of Poa annua and their Putative Ancestors Poa infirma andPoa supina

Flowering responses of two Australian and six Norwegian populationsof Poa annua and their putative ancestors P. infirma and P.supina were studied in controlled environments. The two Australianpopulations originating from suburban parks in Canberra hadopposite daylength flowering responses across the range of temperaturestested (9–21 °C), one being a quantitative short-day(SD) plant with no response to vernalization, the other a quantitativelong-day (LD) plant with a quantitative vernalization requirement(winter annual type). Variation in earliness of flowering withinthe former population was shown to be genetically determined,and testing of selfed progenies indicated that the populationis an aggregate of several largely homozygous lines with divergentflowering responses. Two lowland populations from southern Norwaywere both quantitative LD plants with no vernalization response,while two alpine snowbed populations from southern Norway andtwo high-latitude, subarctic populations from northern Norwaywere quantitative SD plants with an obligatory plant vernalizationor SD requirement for flowering. Two populations of P. supinaexhibited the same flowering responses as the alpine and high-latitudepopulations of P. annua with an obligatory plant vernalizationor SD requirement for flowering. A combination of SD and lowtemperature (9–12 °C) for 8–10 weeks was optimalfor induction and inflorescence initiation. On the other hand,P. infirma was found to be an early-flowering quantitative SDplant which flowered freely across the range of temperatures(9–21 °C) as a typical summer annual. The experimentsdemonstrate that virtually any kind of photoperiodic and vernalizationresponses can be found among populations of P. annua. Theseversatile flowering responses reflect the contrasting floweringresponses of P. supina and P. infirma, and add strong supportto the hypothesis that P. annua has originated from these species.Copyright 2001 Annals of Botany Company Adaptation, evolution, flowering, Poa annua, P. infirma, P. supina, photoperiod, vernalization     

Changes in nucleic acids, protein-nitrogen and amino-nitrogen of excised winter wheat embryos during vernalization

Embryos excised from winter wheat grains were vernalized for10–50 days with or without sugar (sucrose). Determinationswere made of fresh weight, protein-nitrogen, amino-nitrogen,RNA and DNA. There was no change in the contents of RNA of wheatembryos during the vernalization. The incorporation of ³²P intonucleic acid in wheat embryos during vernalization in the presenceof sugar was much higher than that of embryos vernalized withoutsugar. From these results we assumed that RNA turnover occurredduring the vernalization. There was no significant differencein the nucleotide composition of RNA extracted between the vernalizedand unvernalized embryos. The RNA of wheat embryos was separatedinto two fractions. Proportions of these two RNA fractions variedin the course of cold treatment, and similar changes were foundin developing wheat leaves. (Received July 25, 1974; )     

Temperature Response of Vernalization in Wheat: A Developmental Analysis

The vernalization response of wheat ( Triticum aestivum L.)was reinterpreted from a developmental perspective, using currentconcepts of the developmental regulation of wheat morphologyand phenology. At temperatures above 0 °C, the effects ofthe process of vernalization per se in wheat are confoundedby the effects of concurrent vegetative development. These effectsare manifested by differences in the number of leaves initiatedby the shoot apex prior to floral initiation, which in turnaffects the subsequent rate of development to ear emergenceand anthesis. Leaf primordia development during vernalizationand total leaf number at flowering were used to develop criteriato define both the progress and the point of saturation of thevernalization response. These criteria were then used to reinterpretthe results of Chujo ( Proceedings of the Crop Science Societyof Japan 35 : 177–186, 1966), and derive the temperatureresponse of vernalization per se for plants grown under saturatinglong day conditions. The rate of vernalization increased linearlywith temperature between 1 and 11 °C, such that the timetaken to saturate the vernalization response decreased from70 d at 1 °C to 40 d at 11 °C. The rate declined againat temperatures above 11 °C, and 18 °C was apparentlyineffective for vernalization. Total leaf number at saturation,however, increased consistently with temperature, as a resultof the balance between the concurrent processes of leaf primordiuminitiation and vernalization. Total leaf number at saturationincreased from 6 at 1 °C to 13.3 at 15 °C, which inturn influenced the time taken to reach ear emergence. The advantagesof using this developmental interpretation of vernalizationas the basis for a mechanistic model of the vernalization responsein wheat are discussed. Triticum aestivum L.; wheat; vernalization; rate; temperature; primordia; leaf number; flowering