Effects of Temperature and Photoperiod on Flowering in Soya bean [Glycine max (L.) Merrill]: a Quantitative Model

Factorial combinations of five photoperiods (8 h 20 min, 10h, 11 h 40 min, 13 h 20 min and 15 h) and three night temperatures(14, 19 and 24 C) combined with a single day temperature (30C) were imposed on nodulated plants of nine soya bean genotypes[Glycine max (L.) Merrill] grown in pots in growth cabinets.The times to first appearance of open flowers were recorded.For a photoperiod-insensitive cultivar, and for the remainingeight photoperiod-sensitive genotypes in photoperiods shorterthan the critical daylength, the rates of progress towards flowering(the reciprocals of the times taken to flower) were linear functionsof mean diurnal temperature. For all photoperiod-sensitive genotypes,times to flowering in photoperiods longer than the criticaldaylength increased as inverse functions of both increasingphotoperiod and decreasing temperature. A consequence of thesetwo relations is that the critical daylength becomes longerwith higher mean temperatures. In the five photoperiod-sensitivegenotypes which flowered in all environments before the experimentwas terminated (after 150 d) the delays in flowering due tolow temperatures or long photoperiods were limited by a maximumperiod to flowering specific for each genotype. These resultsare discussed in relation to the development of a simple techniquefor the large-scale screening of soya bean germplasm to determinephoto-thermal response surfaces for flowering. Glycine max (L.) Merrill, soya bean, flowering, photoperiod, temperature, screening, germplasm     

Turnover of Storage Protein in Seeds of Soya Bean and Pea

We were interested in determining whether the low protein contentof pea seeds (Pisum sativum L.) as compared to soya bean seeds(Glycine max L. Merrill) might be due to faster degradationof the pea storage proteins during development of the seed.Pea and soya bean cotyledons were subjected to a ‘pulse-chase’experiment using [³H]glycine in in-vitro cultures. In peas,legumin had a half-life of 146 days, while vicilin had a half-lifeof 39 days. There was no measureable degradation of soya beanstorage proteins. Even with the pea storage proteins, the half-liveswere so much longer than the maturation time of seeds that degradationof storage proteins could not account for the lower proteincontent of peas as compared to soya beans. The validity of theseresults was indicated by the finding that non-storage proteinshad much shorter half-lives and that omission of a carbon ora nitrogen source greatly accelerated degradation. Labelledglycine was found to be a good probe for protein turnover studiesbecause it was very rapidly metabolized. Glycine max L. Merrill, soya bean, Pisum sativum, L. pea, protein turnover, storage proteins, legumin, vicilin     

Effects of Nitrate Level on Nitrogen Metabolism in Winged Bean and Soya Bean

The effects of high (15 mM) and low (0.75 mM) solution nitratelevels on nitrogen metabolism in three genotypes (IL 7A, IL13 and IL 21) of winged beans [Psophocarpus tetragonolobus (L.)DC.] and one genotype (Williams) of soya bean [Glycine max (L.)Merrill] were investigated. Plants were grown for 42 days ina greenhouse in solution culture prior to sampling. The 15 mM nitrate treatment resulted in greater growth of allplant parts except roots. Growth of soya beans was more responsiveto nitrate level than was growth of winged beans. The high nitratelevel inhibited nodulation in all plants. The IL 13 and IL 21winged bean genotypes had similar nitrogenase activity (acetylenereduction per plant) as the soya bean and IL 7A winged beangenotype had lower activity. However, the IL 13 winged beangenotype had higher nitrogenase activity (acetylene reductionper unit nodule mass) than the other three genotypes which allhad similar activity. The 15 mM solution nitrate level stimulatedleaf and root nitrate reductase (NR) activity for all plants.All winged bean genotypes had higher leaf NR activity and higherpercentage reduced- and nitrate-nitrogen contents of leavesand stems compared with soya beans. However, total protein (reducednitrogen) was greater in soya beans when sampled indicatingthat more nitrate had been metabolized by soya beans than bywinged beans during the 42-day growth period. Psophocarpus tetragonolobus (L.) DC., winged bean, Glycine max (L.) Merrill, Soya bean, nitrate reductase, nitrogen fixation, nitrogenase activity, nodulation     

The Effect of Adenine and Mevalonic acid on the Endogenous Cytokinins of a Cytokinin-dependent Strain of Soya Bean Callus

The combined application of 10^–6 M adenine and 10^–6M mevalonic acid to soya bean callus accelerated its growth.Two biologically active compounds that co-chromatographed withzeatin and isopentenyl adenine were extracted from this callus.Studies with labelled adenine and mevalonic acid indicated thatthe cytokinin-dependent soya bean callus incorporated only avery small amount of the radioactive precursors into the biologically-activecompounds, making it extremely difficult to determine whetherthese compounds were synthesized de novo or whether they aroseas by-products of tRNA turnover. As cytokinins do not accumulatein rapidly-growing cytokinin-dependent soya bean callus culturedon kinetin as a source of cytokinin it seems as if biosynthesisde novo occurs when the callus is supplied with adenine andmevalonic acid. Glycine max (L.) Merrill, soya bean, callus culture, adenine, mevalonic acid, endogenous cytokinins     

Assumptions of Plastochron Index: Evaluation With Soya Bean Under Field Drought Conditions

Erickson and Michelini (1957) derived the plastochron index(PI) and a term sometimes referred to as the plastochron ratio(PR), as quantitative expressions of the vegetative developmentof plants. With the stable plant growth in environmental chambersand glasshouses, the assumptions used to derive these termshave been validated. However, more recently these expressionsare being used to characterize growth under the unstable conditionsresulting from the imposition of stress. This study examinesthe validity of the assumptions used to derive PI and PR forfield-grown soya beans [Glycine max (L.) Merrill] subjectedto drought stress. Under stress conditions, the assumptionswere not satisfied. In fact, observing change in PR appearedto be a good method for detecting drought stress in these plants.An alternate method for calculating PI based on a single, youngleaf was developed. This alternate method appeared to be a moresensitive indicator of changes in leaf emergence rate underunstable conditions. Plastochron index, plastochron ratio, Glycine max (L.), soya bean, drought, leaf growth     

Periods of Shoot Chilling Sensitivity in Soybean Flower Development, and Compensation in Yield after Chilling

Soybeans [Glycine max (L.) Merr. cv. Ransom] grown at a constant25 °C were placed in a 12-h inductive photoperiod at twoweeks of age. Subgroups were shoot-chilled for one week at aconstant 10 °C during each of the first four weeks of floralinduction. Controls were photoinduced but not chilled. Chillingduring the first week of photoinduction inhibited productionof floral primordia, but did not increase the abscission rateof flowers and pods. Chilling during the second week did notaffect primordium production or abscission rate, but did causea significant increase in numbers of fused and malformed pods.Chilling during the third week caused loss of 77 per cent ofearly flowers and pods by abscission, while fourth week chillingcaused less severe losses by abscission. Inhibition of vegetativegrowth may have been responsible for primordium loss in first-weekplants, while disturbances in the development of flowers wereresponsible for the losses in the other chilling weeks. Althoughchilling during the first and third photoinduction weeks causeda significant reduction in early pod numbers, plants harvestedat 16 weeks of age showed no significant loss in seed yield.Low abscission rates late in pod filling and increased weightof individual seeds compensated for early losses of pods. Thesecompensatory responses to a chilling-induced loss of pods aresimilar to those reported for mechanically depodded soybeans. Glycine max (L.) Merr., soybean, temperature, chilling, floral initiation, anthesis, abscission, yield, compensation     

Photoperiod and the Determination of Potential Seed Number in Chenopodium rubrum L.

Individuals from two latitudinal populations of Chenopodiumrubrum, a short-day annual, were induced in two inductive photoperiods,15 h and 12 h, to examine the dynamics of reproductive developmentthat determine the potential number of seeds produced. The northernpopulation (50° N) is induced in both photoperiods, whilethe southern population (34° N) is induced only in the 12h photoperiod. Individuals were given either 2, 6, 10 or continuousinductive cycles and dissected at intervals after the startof inductive treatments to determine the rates of initiationand differentiation of primordia on the main axis and selectedaxillary buds. Initial reproductive data indicated that the duration of reproductivedevelopment among individuals of the northern population, whengrown in the longer photoperiod, was 25 per cent greater, butthe number of seeds was increased by a factor of 46. Likewisethe duration of reproductive development among individuals ofthe southern population, when grown in the same photoperiodas the northern population, was 50 per cent longer and the numberof seeds was increased by a factor of 66. Dissection of reproductively-developing individuals revealedthat induction leads to a stimulation in the rate of initiationof primordia followed by a complete inhibition coincident withthe differentiation of terminal floral structures. The timingof this stimulation-inhibition process on each axillary buddepends upon its age relative to the timing of induction. Thuscertain primordia on individuals prematurely removed from inductivetreatments escape floral differentiation and remain vegetative.The total number of floral primordia (potential number of seeds)is determined early in reproductive development by (1) the numberof axillary buds at the start of induction, (2) the stimulatedrate of initiation of primordia after induction, and (3) therate of differentiation of induced primordia. Among individuals of the northern population, the longer inductivephotoperiod leads to a greater stimulation in the rate of primordialinitiation and a decrease in the rate of floral differentiation,which together lead to the production of more primordia. Likewiseamong individuals of the southern population in the shorterphotoperiod, the rate of organ initiation is similar to thatof the northern population in the same photoperiod, but therate of floral differentiation is lower, leading to the initiationof many more primordia. The effects of photoperiod on seed number are discussed in termsof physiological and ecological criteria of optimality. Sincenatural induction occurs in the longest, physiologically-'sub-optimarphotoperiods possible, and this leads to the greatest productionof seeds, it is suggested that the critical photoperiod is amore meaningful focus of interpretation than the physiologically‘optimal’ photoperiod. Of the factors influencing potential seed number, the most significantdifference between the two latitudinal populations is the responseof the rate of floral differentiation to the photoperiod ofinduction. Thus potential seed number in natural populationsis intimately related to the prevailing photoperiods throughthe rates of developmental events. Selection for changes inor maintenance of a particular reproductive ecology must bemediated through developmental responses. Limitations on the potential growth rate of plants are discussedin terms of the ratio of meristematic cells to the total cellpopulation in the plant. Thus the number of growing axillarybuds greatly contributes to the potential growth rate, and thedegree of correlative inhibition is interpreted as a cost ofselection for vertical growth among terrestrial plants competingfor light. By means of a simple model the cost of correlativeinhibition is also discussed in terms of potential seed number.Reproduction is seen as a release from the developmental constraintsrequired by plant form and a stimulation of growth that leadsto a very high production of potential seeds.     

Soya Bean Seed Growth and Maturation In vitro without Pods

Immature Glycine max (L.) Merrill seeds, initially between 50and 450 mg f. wt, were grown and matured successfully in vitro.Excised seeds were floated in a liquid medium containing 5 percent sucrose, minerals and glutamine in flasks incubated at25 °C under 300 to 350 µE m^–2 s^–1 fluorescentlight. During 16 to 21 d in culture, seeds grew to a matured. wt of 100 to 600 mg per seed at an average rate of 5 to 25mg d. wt per seed d^–1 depending on initial size. Growthrates were maximal during the first 8 to 10 d in vitro but declinedwith loss of green colour in the cotyledons. Seed coats rupturedwith rapid cotyledon expansion during the first 2 d in culture.Embryos were tolerant to desiccation and 80 to 90 per cent germinatedif removed from culture before complete loss of green colour.The growth of excised seeds in vitro exceeded the growth ofseeds in detached pods, but when windows were cut in pods topermit direct exposure of seeds to the medium, seed growth wascomparable. Glycine max (L.) Merrill, soya bean, seed culture, seed growth, seed maturation, germination     

Phenological Development in Bambara Groundnut (Vigna subterranea) at Constant Exposure to Photoperiods of 10 to 16 h

The flowering and fruit-set of a bambara groundnut selectionfrom Ankpa, Nigeria, were studied in greenhouses at constantexposure to photoperiods of 10, 12, 12·5, 13, 14 and16 h. The development of embryos was determined in ovaries fromplants under photoperiods of 11·5 h and 14 h. The beginningof flowering, recorded as the number of days from sowing tothe first open flower, was delayed by lengthening the photoperiod.It started 7 d later under 16 h than under 10 h. This differenceincreased during the production of the next nine open flowers.Lengthening the photoperiod also caused a delay in the beginningof fruit development. Under 13 h it was delayed by more than40 d compared with fruit development under 10 h. Some plantsunder 14 and 16 h even failed to produce pods. After the beginningof fruit development dry matter partitioning to pods was substantiallyless under 14 and 16 h photoperiods than under photoperiodsof 13 h or less; this was reflected in a strong reduction ofpod growth rates. Under an 11·5 h photoperiod two groups of ovaries couldbe distinguished. In both, embryo development was identicalup to 17 d after anthesis, but then the embryos in the firstgroup continued to develop until they were full-grown at about41 d after anthesis, whereas the growth of the embryos in thesecond group stopped. Embryo development under a photoperiodof 14 h was similar to that in the ovaries with discontinuedembryo growth under the 11·5 photoperiod. Healthy-lookingembryos were found in ovaries up to 32 d after anthesis undera photoperiod 14 h. From then onwards embryos started to shriveland degenerate. Finally, the ovaries aborted.Copyright 1993,1999 Academic Press Vigna subterranea, Voandzeia subterranea, bambara groundnut, phenology, photoperiod, day-length, embryo development, harvest index, dry matter partitioning     

Studies on the Physiology of Flowering of Timothy (Phleutm pratense L.): I. Influence of Daylength and Temperature on Initiation and Differentiation of the Inflorescence

Spikelet initiation is advanced and the proportion of plantswhich attain the reproductive condition is increased in S. 48timothy by lengthening the photo-period from 14 to 24 hours.In shorter periods of light, reproduction is almost completelyinhibited, and in 8-hour short days plants remain vegetativeeven after 35 weeks. Spikelet initiation at the shoot apex occursafter exposure to 3–5 long days followed by short days.Initiation also occurs when extended daylength is replaced by‘light-breaks’ during long nights, or when a singleleaf is photo-induced while the remainder of the plant receivesshort days. High temperatures promote spikelet initiation incontinuous light; in photoperiods nearer the threshold for floweringthis response is reversed and a rise in temperature from 55°to 75° F. increasingly inhibits reproduction. Once initiationhas occurred, spike differentiation is hastened by increasesin temperature or photoperiod. Internode elongation begins atthe time of spikelet initiation, and is promoted by temperatureand photoperiod. Elongated vegetative shoots may be producedwhen spikelet initiation fails in threshold photoperiods orhigh temperatures.     

The Growth and Development of the Wheat Apex: The Effects of Photoperiod on Spikelet Production and Sucrose Concentration in the Apex

Spring wheat (Triticum aestivum cv. Warimba) plants were grownin a controlled environment (20°C) in two photoperiods (8or 16 h). In the first instance, plants were maintained in eachof the photoperiods from germination onwards at the same irradiance(375 µE m^–2 s^–1). In the second case, allplants were grown in a long photoperiod until 4 days after double-ridgeinitiation when half the plants were transferred to a shortphotoperiod with double the irradiance (16 h photoperiod at225 or 8 h at 475 µE ^–2 s^–1). The rates of growth and development of the apices were promotedby the longer photoperiod in both experiments. Shoot dry weightgain was proportional to the total light energy received perday whereas the dry weight of the shoot apex increased withincreasing photoperiod even when the total daily irradiancewas constant. The principal soluble carbohydrate present in the shoot apexwas sucrose, although low concentrations of glucose and fructosewere found in the apices of long photoperiod plants late indevelopment. Sucrose concentration was invariably greater inthe slow-growing apices of short photoperiod plants, but roseto approach this level in the long photoperiod plants when theterminal spikelet had been initiated. Triticum aestivum, wheat, apex, spikelet initiation, photoperiod, flower initiation     

Changes in Apical Growth and Phyllotaxis on Flowering and Reversion in Impatiens balsamina L.

When plants of Impatiens balsamina L were subjected to 5 shortdays and then re-placed in long days, they began to form a terminalflower and then reverted to vegetative growth at this terminalshoot apex The onset of flowering was accompanied by an increasein the rate of initiation of primordia, an increase in the growthrate of the apex, a change in primordium arrangement from spiralto whorled or pseudo-whorled, a lack of internodes, and a reductionm the size at initiation of the primordia and also of the stemfrusta which give rise to nodal and internodal tissues On reversion,parts intermediate between petals and leaves were formed, followedby leaves, although in reverted apices the size at initiationand the arrangement of primordia remained the same as in thefloweing apex The apical growth rate and the rate of primordiuminitiation were less in the reverted apices than in floral apicesbut remained higher than in the original vegetative apex Sincethe changes in apical growth which occur on the transition toflowering are not reversed on reversion, the development oforgans as leaves or petals is not directly related to the growthrate of the apex, or the arrangement, rate of initiation orsize at initiation of primordia Impatiens balsamina L, flower reversion, evocation, phyllotaxis, shoot meristem     

Control of Seed Growth in Soya Beans [Glycine max (L.) Merrill]

The seed is the primary sink for photosynthate during reproductivegrowth and an understanding of the mechanisms controlling therate of seed growth is necessary to understand completely theyield production process. The growth rate of individual seedsof seven soya bean [Glycine max (L.) Merrill] cultivars withgenetic differences in seed size varied from 10.8 to 3.9 mgseed^–1 day^–1. The growth rates were highly correlatedwith final seed size. The growth rate of cotyledons culturedin a complete nutrient medium was highly correlated with thegrowth rate of seeds developing on the plant and with finalseed size. The number of cells per seed in the cotyledons variedfrom 10.2 to 5.7 x 10⁶ across the seven cultivars. The numberof cells per seed in the cotyledons was significantly correlatedwith final seed size and the seed growth rate both on the plantand in the culture medium. The data suggest that genetic differencesin seed growth rates are controlled by the cotyledons and thenumber of cells in the cotyledons may be the mechanism of control. Glycine max L., soya bean, seed size, growth rate, cell number, sink activity     

Influence of Photoperiod on Culm Elongation and Apical Development in Semi-dwarf and Standard-height Wheats

Flower initiation (FI) coincided with the commencement of culmelongation under both long (18 h) and normal (104–144h) photoperiod in eight spring wheats, including both gibberellicacid-sensitive and -insensitive types, which differed widelyin photoperiod sensitivity At FI the apex was significantly (P = 005) higher (above ground)in three of the wheats under long, compared with normal photoperiod;with no difference between the remaining five. Differences inresponse were not related to photoperiod response or gibberellicacid-sensitivity/insensitivity differences between the wheats. Long photoperiod prolonged the phase from terminal spikeletinitiation (TSI) to anthesis (A) in all the wheats, except Sunset(with the greatest photoperiod insensitivity), with no cleardifferences in response between semi-dwarf and standard-heightwheats. Respective rates of culm elongation from FI to TSI were lowerunder normal, compared with long, photoperiod in all varieties.That from TSI to A was unaffected by photoperiod, except inSunset when it was significantly (P = 001) slower under long,compared with normal photoperiod. Rate of culm elongation from FI to TSI across cultivars andphotoperiods was inversely related to spikelet number per head(r = –053, P = 005) but not to rate of spikelet initiation(r = –014 n.s.). Gibberellin-sensitivity, spikelet number, flower initiation, terminal spikelet initiation     

A Dynamic Growth Model of Vegetative Soya Bean Plants: Model Structure and Behaviour under Varying Root Temperature and Nitrogen Concentration

A differential equation model of vegetative growth of the soyabean plant (Glycine max (L.) Merrill cv. ‘Ransom’)was developed to account for plant growth in a phytotron systemunder variation of root temperature and nitrogen concentrationin nutrient solution. The model was tested by comparing modeloutputs with data from four different experiments. Model predictionsagreed fairly well with measured plant performance over a widerange of root temperatures and over a range of nitrogen concentrationsin nutrient solution between 0.5 and 10.0 mmol in the phytotron environment. Sensitivity analyses revealedthat the model was most sensitive to changes in parameters relatingto carbohydrate concentration in the plant and nitrogen uptakerate. Key words: Glycine max (L.) Merrill, dry matter, nitrogen uptake, partitioning, photosynthesis, respiration, sensitivity analysis     

Effects of Photoperiod, Nitrogen Nutrition and Temperature on Inflorescence Initiation and Development in Onion (Allium cepa L.)

The effects of photoperiod, nitrogen nutrition and temperatureon inflorescence initiation and development in onion cv. Rijnsburgerand cv. Senshyu Semi-globe Yellow were studied in controlledenvironments. Rates of inflorescence initiation were estimatedusing the data for leaf numbers formed prior to flower formationand the rates of leaf initiation. At 9 °C inflorescenceinitiation was accelerated by long photoperiods particularlyfor cv. Rijnsburger where the average time for initiation was86 days in 8 h and 38 days in 20 h photoperiods. Initiationwas as rapid at 12 °C as at 9 °C but was slower at 6°C. A reduction in the nitrate concentration in the nutrientsolution from 0.012 to 0.0018 M greatly accelerated inflorescenceinitiation particularly in photoperiods and temperatures notconducive to rapid initiation. Cv. Senshyu initiated more slowlythan cv. Rijnsburger and was less sensitive to photoperiod andnitrogen level. The development rate of inflorescences afterinitiation was accelerated by long photoperiods and increasesin temperature from 6 to 12 °C but was retarded by the lowernitrogen level. Allium cepa L., onion, flower initiation, inflorescence development, photoperiod, nitrogen nutrition, temperature, vernalization     

Histochemical Study of Photoperiodic and Low Temperature Effects on Floral Induction of Spinacia oleracea

Shoot apices of Spinacia oleracea plants have been induced toflower either by: (a) subjecting leaves to 24 h long day, or(b) exposure to a short photoperiod but displaced by 8 h (displacedshort day) in the usual 24 h short-day cycle, or (c) exposureto low temperature (5 °C) during the dark period of thenormal short day. A quantitative cytochemical assay of pentosephosphate pathway activity during floral induction indicatesan approximate doubling of the rate of activity when comparedto that of vegetative apices (short day) (21 °C). Exposure to either low temperature, or a displaced short photoperiodstimulates pentose phosphate pathway activity in the shoot apexin a manner similar to that seen by long-day induction. Thischange in metabolic activity is accompanied by changes in theshape of the shoot apex which resembles that seen at an earlystage during floral induction. Spinacia oleracea, pentose phosphate pathway, shoot apex, glucose-6-phosphate dehydrogenase, floral induction, chilling, displaced short day     

Reversion of flowering in Glycine Max (Fabaceae)

Photoperiodic changes, if occurring before a commitment to flowering is established, can alter the morphological pattern of plant development. In this study, Glycine max (L.) Merrill cv. Ransom plants were initially grown under an inductive short-day (SD) photoperiod to promote flower evocation and then transferred to a long-day (LD) photoperiod to delay flower development by reestablishing vegetative growth (SD-LD plants). Some plants were transferred back to SD after 4-LD exposures to repromote flowering (SD-LD-SD plants). Alterations in organ initiation patterns, from floral to vegetative and back to floral, are characteristic of a reversion phenomenon. Morphological features that occurred at the shoot apical meristem in SD, LD, SD-LD, and SD-LD-SD plants were observed using scanning electron microscopy (SEM). Reverted plants initiated floral bracts and resumed initiation of trifoliolate leaves in the two-fifths floral phyllotaxy prior to terminal inflorescence development. When these plants matured, leaf-bract intermediates were positioned on the main stem instead of trifoliolate leaves. Plants transferred back to a SD photoperiod flowered earlier than those left in LD conditions. Results indicated that in plants transferred between SDs and LDs, photoperiod can influence organ initiation in florally evoked, but not committed, G. max plants.     

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.     

Effects of Photoperiod, Temperature and Asynchrony between Thermoperiod and Photoperiod on Development to Panicle Initiation in Sorghum

The duration of the vegetative phase (i.e. days from sowingto panicle initiation) in sorghum [Sorghum bicolor (L.) Moench]is affected by photoperiod and temperature. Plants of severalcontrasting genotypes of sorghum were grown in controlled-environmentgrowth cabinets with either synchronous or asynchronous photoperiodsand thermoperiods. Apical development was recorded. Diurnalasynchrony between photoperiod and thermoperiod reduced durationsto panicle initiation when the temperature warmed after lightswent on and cooled after lights went off, but increased thesedurations when the temperature warmed before lights went onand cooled before lights went off. These effects were shownin the maturity lines 60M and SM100 and also in the USA cv.RS610 and the Sudanese landrace IS22365, but their magnitudevaried with genotype, photothermal regime, and the degree ofasynchrony. The greatest effect was detected in IS22365 grownat 30/21 °C (12 h/12 h) with a 12 h d^-1photoperiod whenthe temperature warmed 2.5 h before lights went on and cooled2.5 h before lights went off, when the duration from sowingto panicle initiation was 69 d compared with 37 d in the control(synchronous photoperiod and thermoperiod in each diurnal cycle). Reciprocal transfers of plants of IS22365 between short andlong days revealed that asynchrony principally affected theduration of the photoperiod-insensitive pre-inductive phaseof development; i.e. asynchrony affected the time (age) at whichthe plants were first able to respond to photoperiod. In thatinvestigation in controlled-environment growth chambers, thesubsequent photoperiod-sensitive inductive phase continued untilpanicle initiation. Subsequent reciprocal transfer experimentsin controlled-environment glasshouses in four different alternatingtemperature regimes employed synchronous photoperiods and thermoperiodsin short (11 h) days with temperature warming 1.5 h after thebeginning of the day in long (12.5 h) days. In those investigations,photoperiod sensitivity ended some time before (2.5–8.1d, mean 5.7 d) panicle initiation in IS22365, Naga White andSeredo. Moreover, whereas the duration of the photoperiod-insensitivepre-inductive phase was affected by temperature, the durationsof the photoperiod-sensitive inductive and the photoperiod-insensitivepost-inductive phases were not. Sorghum bicolor (L.) Moench; sorghum; asynchrony; photoperiod; thermoperiod; vegetative phase; panicle initiation