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.     

Effects of Temperature and Photoperiod on Flowering in Chickpeas (Cicer arietinum L.)

Factorial combinations of two photoperiods (12 and 15 h), threeday temperatures (20, 25 and 30 °C) and three night temperatures(10, 15 and 20 °C) were imposed on nodulated plants of ninechickpea genotypes (Cicer arietinum L.) grown in pots in growthcabinets. The times to first appearance of open flowers wererecorded. For all genotypes, the rates of progress towards flowering(the reciprocals of the times taken to flower) were linear functionsof mean temperature. There were no interactions between meantemperature and photoperiod but the longer photoperiod increasedthe rate of progress towards flowering. These effects were independentof both radiation integral (the product of irradiance and photoperiod)and the vegetative stature of the plant. Taken in conjunctionwith evidence from work on other long-day species, it is suggestedthat the photo-thermal response of flowering in chickpeas, overthe range of environments normally experienced by the crop,may be described by the equation: 1/f = a+b     

Environmental Control of Flowering in Barley (Hordeum vulgare L.). I. Photoperiod Limits to Long-day Responses, Photoperiod-insensitive Phases and Effects of Low-temperature and Short-day Vernalization

Barley plants were grown at a mean diurnal temperature of 15°C and reciprocally transferred between different photoperiods(from 16 h d^–1 to 8, 10 or 13 h d^–1 or vice versaat 4, 8, 16 or 32 d after germination). Ten contrasting genotypeswere examined, including seven spring-sown types-Mona, BGS T16-2,Athenais, Emir, Funza, USDA-016525 and S-37, and three autumn-sowntypes-Gerbel B, Arabi Abiad and Ager. In the latter two alltreatments were repeated on plants grown from seeds which hadbeen vernalized at 2 °C for 42 d. The results suggest that, between the critical photoperiod (belowwhich there is a delay in flowering) and the ceiling photoperiod(below which there is no further delay), there is a linear relationbetween photoperiod and the reciprocal of the time taken toflower (awn emergence). In all genotypes the ceiling photoperiodwas     

Interaction of vernalization, photoperiod and high temperature in flowering of Arabidopsis thaliana (L.) HEYNH.

Flowering of Arabidopsis thaliana (L.) HEYNH., var. "Stockholm",plants, raised from vernalized seeds, may be modified by thephotoperiodic conditions or a short (1 week) exposure to hightemperature (32°C) following vernalization, depending onthe duration of the cold treatment. When vernalization is partial(1 to 4 weeks at 4°C), both short days (8hr light) and hightemperature have a devernalizing effect, but when the cold requirementhas been fully satisfied, after 5 to 6 weeks at 4°C, devernalizationis no longer possible. There is no interaction between photoperiodand high temperature. Fully vernalized plant flower in bothlong and short days, although flowering is delayed in shortdays. This delay is not a photoperiodic effect, however, butmay be ascribed to the decreased radiant energy available inan 8-hr photoperiod. Thus, fully vernalized Arabidopsis plantsare day-neutral. (Received November 5, 1969; )     

Effects of Temperature and Photoperiod on Flowering in Lentils (Lens culinaris Medic.)

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 (cultivars and land-races) of lentil (Lens culinarisMedic.) grown in pots in growth cabinets from vernalized (1.50.5 C for 30d) or non-vernalized seeds (i.e. 144 ‘treatment’combinations). The times from sowing to the appearance of firstopen flowers were recorded. Vernalization, long days and warmtemperatures hastened flowering but genotypes differed in relativesensitivity to each of these factors and in time to floweringin the same most-inductive environment. Rates of progress towardsflowering (i.e. 1/f the reciprocals of the times to first flower,f) in all genotypes, vernalized or not, were linear functionsof both mean temperature,     

The Effects of Temperature, Photoperiod and Light Integral on the Time to Flowering of Pansy cv. Universal Violet (ViolaxwittrockianaGams.)

The effects of temperature, photoperiod and light integral onthe time to first flowering of pansy (ViolaxwittrockianaGams)were investigated. Plants were grown at six temperatures (meansbetween 14.8 and 26.1 °C), combined with four photoperiods(8, 11, 14 and 17 h). The rate of progress to flowering increasedlinearly with temperature (up to an optimum of 21.7 °C)and with increase in photoperiod (r²=0.91, 19 d.f.), the latterindicating that pansies are quantitative long day plants (LDPs).In a second experiment, plants were sown on five dates betweenJuly and December 1992 and grown in glasshouse compartmentsunder natural day lengths at six temperatures (means between9.4 and 26.3 °C). The optimum temperature for time to floweringdecreased linearly (from 21.3 °C) with declining light integralfrom 3.4 MJ m^-2d^-1(total solar radiation). Data from both experimentswere used to construct a photo-thermal model of flowering inpansy. This assumed that the rate of progress to flowering increasedas an additive linear function of light integral, temperatureand photoperiod. Independent data from plants sown on threedates, and grown at five temperatures (means between 9.8 and23.6 °C) were used to validate this model which gave a goodfit to the data (r²=0.88, 15 d.f.). Possible confounding ofthe effects of photoperiod and light integral are discussed. Pansy;Violaxwittrockiana; flowering; photo-thermal model; temperature; photoperiod; light integral     

Effects of Temperature and Photoperiod on Phenological Development in Three Genotypes of Bambara Groundnut (Vigna subterranea)

Factorial combinations of four photoperiods (10, 11·33,12·66 and 16 h d^-1) and three mean diurnal temperatures(20·2, 24·1 and 28·1°C) were imposedon nodulated plants of three Nigerian bambara groundnut genotypes[Vigna subterranea (L.) Verdc., syn. Voandzeia subterranea (L.)Thouars] grown in glasshouses in The Netherlands. The photothermalresponse of the onset of flowering and the onset of poddingwere determined. The time from sowing to first flower (f) wasdetermined by noting the day on which the first open flowerappeared. The time from sowing to the onset of podding (p) wasestimated from linear regressions of pod dry weight againsttime from sowing. Developmental rates were derived from thereciprocals of f and p. In two genotypes, 'Ankpa 2' and 'Yola',flowering occurred irrespective of photoperiod and 1/f was controlledby temperature only, occurring sooner at 28·1 than at20·2°C. The third genotype, 'Ankpa 4', was sensitiveto temperature and photoperiod and f was increased by coolertemperatures and photoperiods > 12·66 h d^-1 at 20·2°Cand > 11·33 h d^-1 at 24·1 and 28·1°C.In contrast, p was affected by temperature and photoperiod inall three genotypes. In bambara groundnut photoperiod-sensitivitytherefore increases between the onset of flowering and the onsetof podding. The most photoperiod-sensitive genotype with respectto p was 'Ankpa 4', followed by 'Yola' and 'Ankpa 2'. Therewas also variation in temperature-sensitivity between the genotypesinvestigated. Evaluation of bambara groundnut genotypes foradaptation to different photothermal environments will thereforerequire screening for flowering and podding responses.Copyright1994, 1999 Academic Press Vigna subterranea (L.) Verdc., Voandzeia subterranea (L.) Thouars, bambara groundnut, phenology, photoperiod, daylength, temperature, flowering, podding     

Environmental Control of Flowering in Vicia faba L.

There is a heteroblastic change in leaflet number in many stocksof Vicia faba, the rate of change being affected by the temperatureand photoperiod under which the plants are grown. In all exceptthe earliest flowering stocks of broad beans, and particularlyat high temperatures, flower initiation shows a quantita-tivelong-day response. For full development of the initiated inflorescenceslong days are required. Flower initiation may be accelerated in all except the earliestflowering stocks of V.faba by brief exposures to low temperatures,particularly when the plants are grown in short days at hightemperatures. The response to low temperatures is more rapidat I0° C. than at 4° C. but eventually approaches saturationat both temperatures. More prolonged exposure to low temperaturesdelays flower initia-tion. The response to low temperaturesincreases with increasing plant age but can occur during embryodevelopment on the mother plant. At temperatures above 14° C, and particularly above 23°C, a reaction inhibitory to flower initiation occurs. This reactionis probably restricted to the diurnal dark periods but is operativeat all stages of the life cycle, including embryo development.Its inhibitory effects may be overcome by subsequent cold treatment,and when the low temperature processes have reached saturationsubsequent high temperatures are no longer inhibitory. Although nucleosides could accelerate flower initiation, purineand pyrimidene analogues did not, with one exception, reducethe response to low temperature treatment.     

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     

The Effects of Temperature and Light Integral on the Phases of Photoperiod Sensitivity inPetuniaxhybrida

Flowering in petunias is hastened by long days, but little isknown about when the plants are most sensitive to photoperiod,or how light integral or temperature affect such phases of sensitivity.The effects of these factors on time to flowering was investigatedusing reciprocal transfer experiments between long (16 h d^-1)and short days (8 h d^-1). The effect of light integral on thephases of photoperiod sensitivity was examined using two sowingdates and a shading treatment (53% transmission). The effectsof temperature were investigated by conducting reciprocal transferexperiments in glasshouse compartments at five temperature regimes(means of 13.7, 19.2, 22.3, 25.0 and 28.7 °C). The lengthof the photoperiod-insensitive juvenile phase of development,when flowering cannot be induced by any environmental stimulus,was sensitive to light integral; low light integrals prolongedthis phase, from 23 d at 2.6 MJ m^-2d^-1to 36 d at 1.6 MJ m^-2d^-1(totalsolar radiation). The length of this development phase was shortest(12.5 d) at 21 °C; it was longer under cooler (21 d at 13.5°C) and warmer temperatures (17.6 d at 28.3 °C). Afterthis phase, time to flowering was influenced greatly by photoperiod,with long days hastening flowering by between 28 and 137 d,compared with short days. Plants also showed some sensitivityto both temperature and light integral during this phase, butthe duration of the final phase of flower development, duringwhich plants were photoperiod-insensitive, was dependent primarilyon the temperature at which the plants were grown; at 14.5 °C,33.9 d were required to complete this phase compared with 11.4d at 25.5 °C. The experimental approach gave valuable informationon the phases of sensitivity to photothermal environment duringthe flowering process, and could provide the basis of a morephysiologically-based quantitative model of flowering than hashitherto been attempted. The information is also useful in thescheduling of lighting and temperature treatments to give optimalflowering times of high quality plants.Copyright 1999 Annalsof Botany Company Petunia,Petuniaxhybrida, juvenility, flowering, photoperiod, temperature, light integral, reciprocal transfer.     

Day and Night Temperature Control of Floral Induction in Stylosanthes guianensis var. guianensis cv. Schofield

Floral initiation in seedlings of Stylosanthes guianensis var.guianensis cv. Schofield grown at a photoperiod marginal forflowering (12–11.75 h) was promoted by a combination oflow day (25 °C) and low night (16 or 21 °C) temperatures,and completely inhibited by a 35 °C day temperature. Additionally,earliness of floral initiation under naturally decreasing daylengthwas negatively related to temperature regime over the range35/30 to 20/15 °C (day/night). Stylosanthes guianensis var, guianensis, flowering, temperature, photoperiod, short-day plant     

Effects of NaCl on Growth, Nitrogen Incorporation and Chemical Composition of Inoculated and NH4NO3 Fertilized Vicia faba (L. ) Plants

Vicia faba cv. Maris Bead was grown either on fixed nitrogenor on ammonium nitrate. After 4 weeks growth, nutrient solutionswere supplemented with 50, 75 and 100 mol m^–3 NaCl for15 d. Five harvests were made at weekly intervals, beginningat 4 weeks. Effects of salinity were directly related to dose,plant growth (fresh and dry weight) being depressed in bothN-fixing and N-fertilized plants. The number of nodules perplant and the proportion of those formed which developed intothe active nitrogen fixing state were depressed by salt stress.Increased size of nodules in salt-stressed plants only partlycompensated for the lower specific nitrogenase activity. Theeffects of salinity on plant nitrogen content were more pronouncedon N-flxing than on N-fertilized plants. The former took upmore Na⁺ and Cl^– than the latter: the implications ofthis and of ionic imbalance are discussed. Key words: Vicia faba, Growth, Salt stress, Nodulation     

Developmental Regulation of Low-temperature Tolerance in Winter Wheat

Vernalization and photoperiod genes have wide-ranging effectson the timing of gene expression in plants. The objectives ofthis study were to (1) determine if expression of low-temperature(LT) tolerance genes is developmentally regulated and (2) establishthe interrelationships among the developmental stages and LTtolerance gene expression. LT response curves were determinedfor three photoperiod-sensitive LT tolerant winter wheat (Triticumaestivum L. em Thell) genotypes acclimated at 4 °C under8 h short-day (SD) and 20 h long-day (LD) photoperiods from0 to 112 d. Also, three de-acclimation and re-acclimation cycleswere used that bridged the vegetative/reproductive transitionpoint for each LD and SD photoperiod treatment. A vernalizationperiod of 49 d at 4 °C was sufficient for all genotypesto reach vernalization saturation as measured by minimum finalleaf number (FLN) and confirmed by examination of shoot apicesdissected from crowns that had been de-acclimated at 20 °CLD. Before the vegetative/reproductive transition, both theLD- and SD-treated plants were able to re-acclimate to similarLT₅₀(temperature at which 50% of the plants are killed by LTstress) levels following de-acclimation at 20 °C. De-acclimationof LD plants after vernalization saturation resulted in rapidprogression to the reproductive phase and limited ability tore-acclimate. The comparative development of the SD (non-flowering-inductivephotoperiod) de-acclimated plants was greatly delayed relativeto LD plants, and this delay in development was reflected inthe ability of SD plants to re-acclimate to a lower temperature.These observations confirm the hypothesis that the point oftransition to the reproductive stage is pivotal in the expressionof LT tolerance genes, and the level and duration of LT acclimationare related to the stage of phenological development as regulatedby vernalization and photoperiod requirements. Copyright 2001Annals of Botany Company Triticum aestivum L., wheat, low-temperature tolerance, vernalization, photoperiod, phenological development     

Photoperiod Sensitivity during Flower Development of Opium Poppy (Papaver somniferum L.)

Photoperiod is a major factor in flower development of the opiumpoppy (Papaver somniferum L. ‘album DC’) which isa long-day plant. Predicting time to flower in field-grown opiumpoppy requires knowledge of which stages of growth are sensitiveto photoperiod and how the rate of flower development is influencedby photoperiod. The objective of this work was to determinewhen poppy plants first become sensitive to photoperiod andhow long photoperiod continues to influence the time to firstflower under consistent temperature conditions. Plants weregrown in artificially-lit growth chambers with either a 16-hphotoperiod (highly flower inductive) or a 9-h photoperiod (non-inductive).Plants were transferred at 1 to 3-d intervals from a 16- toa 9-h photoperiod andvice versa . All chambers were maintainedat a 12-h thermoperiod of 25/20 °C. Poppy plants becamesensitive to photoperiod 4 d after emergence and required aminimum of four inductive cycles (short dark periods) beforethe plant flowered. Additional inductive cycles, up to a maximumof nine, hastened flowering. After 13 inductive cycles, floweringtime was no longer influenced by photoperiod. These resultsindicate that the interval between emergence and first flowercan be divided into four phases: (1) a photoperiod-insensitivejuvenile phase (JP); (2) a photoperiod-sensitive inductive phase(PSP); (3) a photoperiod-sensitive post-inductive phase (PSPP);and (4) a photoperiod-insensitive post-inductive phase (PIPP).The minimum durations of these phases forPapaver somniferum‘album DC’ under the conditions of our experimentwere determined as 4 d, 4 d, 9 d, and 14 d, respectively. Anthesis; days to flowering; flower bud; opium poppy; Papaver somniferum L.; photoperiod; photoperiod sensitivity; predicting time to flowering; transfer     

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.     

Flowering of S. 24 Perennial Ryegrass (Lolium perenne L.) in Short Days at Low Temperature

The flowering of the quantitative long-day plant perennial ryegrass(Lolium perenne L.) in short days (8 h), when grown at low temperature(9/4 °C) and under natural summer daylight, is presentedas evidence for the replacement of specific environmental requirementsfor flowering by alternative stimuli in a grass.     

Effects of Temperature and Photoperiod on Winged Beans [Psophocarpus tetragonolobus (L.) D.C.]

The effects of temperature and photoperiod on winged beans werestudied using 15 University of New Guinea (UPS) selections andfive Sri Lanka (SL) selections. They were grown at 25/20 or30/25 °C day/ night temperature at 11 or 14 h photoperiodwith 12 h thermoperiod. Differences in stomatal density wereobserved among selections and between photoperiods. Higher densitiesoccurred at 14 h photoperiod than at 11 h photoperiod. Whenstomatal density was high due to a photoperiod or temperatureeffect, there was a corresponding increase in leaf area andd. wt of plants. Total chlorophyll content at 25/20 °C was higher at 11 hphotoperiod than at 14 h photoperiod in all selections whilethe total chlorophyll content at 30/25 °C varied with thephotoperiod and selection. Leaf area of SL selections was greater than that of UPS selections.Also greater leaf area was observed at 14 h photoperiod thanat 11 h photoperiod, irrespective of the growing temperature. Temperature was as important as photoperiod in controlling floweringof winged beans. All the UPS selections and two SL selectionsflowered at 11 h photoperiod at 25/20 °C but failed to flowerat the same photoperiod at 30/25 °C indicating an interactionbetween temperature and photoperiod. It is likely that wingedbeans have a narrow photoperiodic range, particularly the SLselections. Psophocarpus tetragonolobus (L.) D.C., winged bean, stomatal density, leaf area, flowering, temperature, photoperiod     

The Influence of Temperature on Seed Germination Rate in Grain Legumes: III. A COMPARISON OF FIVE FABA BEAN GENOTYPES AT CONSTANT TEMPERATURES USING A NEW SCREENING METHOD

Ellis, R. H., Simon, G. and Covell, S. 1987. The influence oftemperature on seed germination rate in grain legumes. III.A comparison of five faba bean genotypes at constant temperaturesusing a new screening method.—J. exp. Bot. 38: 1033–1043. A screening procedure which requires information on the progressof germination at only four temperatures was able to definethe response of the rate of seed germination to sub- and supra-optimaltemperatures for whole seed populations of each of five fababean (Vicia faba L.) genotypes. In one population of the cultivarSutton the models for sub- and supra-optimal temperatures derivedfrom the screen satisfactorily explained observations from anearlier separate investigation at a wider range of temperatures.Two discrete groups of genotypes were identified. Within eachgroup the base temperature T_b did not differ significantly:for the landraces Lebanese Local Large and Syrian Local Largethe value was estimated to be –7·5°C and forthe landrace Lebanese Local Small and the cultivars Sutton andAquadulce it was –4·0°C. The optimum temperaturefor the 50th percentile [T_o(50), at which temperature the rateof germination is maximal] also varied between these two groupsof genotypes, being 20·5–21·5°C forthe first group and 24·5–26·0°C forthe second. In several temperature regimes some of the viableseeds within a seed population failed to germinate. Nevertheless,even at temperatures where a substantial proportion of the seedsfailed to germinate the models defined by the screening methodpredicted the germination times of those seeds which did germinate. Key words: Faba bean, seed gemination rate, temperature     

A Quantitative Model of Reproductive Development in Cowpea [Vigna unguiculata (L) Walp.] in relation to Photoperiod and Temperature, and Implications for Screening Germplasm

Factorial combinations of four photoperiods (10 h, 11 h 40 min,13 h 20 min and 15 h) and three night temperatures (14, 19 and24 °C) combined with a single day temperature (30 °C)were imposed on nodulated plants of 11 cowpea accessions [Vignaunguiculata (L) Walp.] grown in pots in growth cabinets. Thetimes to first appearance of flower buds, open flowers and maturepods were recorded. Linear relationships were established betweenthe reciprocal of the times taken to flower and both mean diurnaltemperature and photoperiod. When the equations describing thesetwo responses are solved, the time to flower in any given photothermalregime is predicted by whichever solution calls for the greaterdelay in flowering. Thus in different circumstances floweringis controlled exclusively by either mean temperature or photoperiod.The value of the critical photoperiod is temperature-dependentand a further equation, derived from the first two, predictsthis relationship. Considered together as a quantitative modelthese relationships suggest simple field methods for screeninggenotypes to determine photo-thermal response surfaces. Vigna unguiculata (L) Walp., cowpea, reproductive development, photoperiod, temperature, germplasm     

Environmental Control of Flowering in Barley (Hordeum vulgare L.). II. Rate of Developement as a Function of Temperature and Photoperiod and its Modification by Low-temperature Vernalization

Plants of six contrasting genotypes of barley were raised fromvernalized (imbibed at 1 °C for 30 d) or non-vernalizedseeds and grown in 12 different controlled environments comprisingfactorial combinations of three photoperiods (10, 13 and 16h d^–1), two day temperatures (18 and 28 °C) and twonight temperatures (5 and 13 °C). Except at longer daysfor Athenais or Arabi Abiad, the 28 °C day temperature wasgenerally supra-optimal and delayed awn emergence. At lowertemperatures and in photoperiods shorter than the critical value,P_C, which delay awn emergence, the time from sowing to awn emergencefor five of the genotypes conformed to the equation 1/f=a +bT{macron}+cPwhere f is the time to awn emergence (d), T{macron} is meandiurnal temperature (°C), P is photoperiod (h d^–1)and a, b and c are genotype-specific constants. In Arabi Abiad,however, significant responses to temperature were not detected.The low temperature pre-treatment of the seeds reduced the subsequenttime to awn emergence in Athenais and the autumn-sown genotypesAger, Arabi Abiad and Gerbel B, especially in longer days, buteither had no effect or tended to delay awn emergence in thespring-sown types Emir and Mona. In the spring-sown types P_Cwas outside the range investigated (i.e. > 16 h d^–1),but in Ager it was approx. 13 h d^–1 and in Gerbel B justover 13 h d^–1. For plants of Arabi Abiad grown from vernalizedseeds P_c was almost 15 h, but