Photoperiod and Temperature Regulation of Floral Initiation and Anthesis in Soya Bean

Floral development includes initiation of floral primordia andsubsequent anthesis as discrete events, even though in manyinvestigations only anthesis is considered. For ‘Ransom’soya bean [Glycine max (L.) Merrill] grown at day/night temperaturesof 18/14, 22/18, 26/22, 30/26, and 34/30 °C and exposedto photoperiods of 10, 12, 14, 15, and 16 h, time of anthesisranged from less than 21 days after exposure at the shorterphotoperiods and warmer temperatures to more than 60 days atlonger photoperiods and cooler temperatures. For all temperatureregimes, however, floral primordia were initiated under shorterphotopenods within 3 to 5 days after exposure and after notmore than 7 to 10 days exposure to longer photoperiods. Onceinitiation had begun, time required for differentiation of individualfloral primordia and the duration of leaf initiation at shootapices increased with increasing length of photoperiod. Whileproduction of nodes ceased abruptly under photoperiods of 10and 12 h, new nodes continued to be formed concurrently withinitiation of axillary floral primordia under photoperiods of14, 15 and 16 h. The vegetative condition at the main stem shootapex was prolonged under the three longer photoperiods and issuggestive of the existence of an intermediate apex under theseconditions. The results indicate that initiation and anthesisare controlled independently rather than collectively by photoperiod,and that floral initiation consists of two independent steps—onefor the first-initiated flower in an axil of a main stem leafand a second for transformation of the terminal shoot apex fromthe vegetative to reproductive condition. Apical meristem, intermediate apex, floral initiation, anthesis, photoinduction, Glycine max(L.) Merrill, soya bean, photoperiod, temperature     

Axillary Bud Inhibition Induced by Young Leaves or Bract in Euphorbia pulcherrima Willd

In plants held under long days in the vegetative stage, youngexpanding leaves of poinsettia (Euphorbia pulcherrima Willd.‘Brilliant Diamond’) are the main source of axillarybud inhibition, while the apical bud, which includes the meristem,primordial leaves and small unfolded leaves, is a secondaryinhibition source. Removal of these expanding leaves resultedin rapid release and growth of axillary buds. Decapitation ofthe apical bud resulted in delayed axillary bud release. Inreproductive plants kept in short days, the pigmented bractsare the primary source of axillary bud inhibition and the cyathiaare the secondary source. Applications of NAA —substitutedfor both young leaves and bract inhibition — maintainedapical dominance. The concentration of endogenous auxin washighest in the apical bud. However, when calculated on wholeorgan basis the auxin level was greater in young developingvegetative leaves and in reproductive bracts than in the apicalbud. Euphorbia pulcherrima Willd, apical bud, apical dominance, auxin, correlative inhibition, cyathia, poinsettia, IAA, NAA     

Effect of decapitation, phosfon D and cycocel on the flowering of Impatiens balsamina exposed to varying numbers of short days

Impatiens balsamina L., a qualitative short day plant, requiresmore short days for the development of floral buds into flowersthan for their initiation. Phosfon D and cycocel reduce thenumber of short days required for flowering, increase the numberof floral buds and flowers and delay their reversion to vegetativegrowth when transferred to noninductive conditions. The effectof decapitation of the main shoot subsequent to the emergenceof floral buds resembles that of retardants indicating thatthe effect of the latter in flower promotion in this plant maybe by virtue of their effect on cessation of apical dominanceas a consequence of which reserve food materials may be channeledto axillary floral buds enabling them to develop into flowers. (Received January 9, 1969; )     

Ontogeny of Tendrils in Antigonon leptopus H. & Arn.

In Antigonon leptopus the main tendrillar and axillary branchis a modified inflorescence axis. It usually bears 6–7lateral bracts out of which 3–4 lower ones are small andleaf-like while the upper 2–3 are tendrillar; 2–3tendrils are also present at its terminal end. The vegetativeshoot apex shows a single layer of tunica and an inner massof corpus without any cytohistological zonation. The earliestaxillary bud or tendril meristem arises at the second node andit elongates due to rib meristem activity. The bract primordiaarise in an acropetal succession. The initiation of the bract-tendriland the leafy bract is similar. In the development of the bract-tendril,marginal meristem activity is absent or reduced and the differentiationof the apical and subapical initials is absent. The terminalbract-tendrils arise as lateral appendages and the residuumof the apical meristem of the main axillary tendril persistsfor some time. In the flowering period the floral buds arisein the axils of the bracts and bract-tendrils. No flowers arepresent in the axils of terminal bract-tendrils.     

Leaf and Floret Production in Sunflower (Helianthus annuus L.) as Affected by Nitrogen Supply

Both the vegetative and the floral meristems of glasshouse-grownsunflowers respond to nitrogen supply in the same way. The durationof leaf and floret production is unaffected but the rate ofproduction is decreased by low nitrogen supply. Thus both finalleaf number and floret number are lowest at the lowest nitrogensupply. The activity of the vegetative meristem is directlyrelated to the content of reduced nitrogen of the plant. Relief of nitrogen stress in the middle of the vegetative phaseallows final leaf number to reach the unstressed number. However,relief of nitrogen stress during floral initiation showed thatfloret number is a function of the plant's content of reducednitrogen at the beginning of floret production. Relief of nitrogenstress from the middle to the end of floret production did notincrease floret number. Nitrogen supply did not influence the duration but did affectthe rate of leaf expansion. Relief of nitrogen stress afterleaf and floral initiation were complete caused a larger finalarea in those leaves still expanding and also lessened apicaldominance so that some axillary buds developed into small flowers. Helianthus annuus L, sunflower, nitrogen supply, leaf production, leaf growth, floret production     

The Carnation Succulent Plantlet -- A Stable Teratological Growth

Axillary buds of carnation (cv. Cerise Royalette) cultured invitro, frequently became ‘succulent’ plantlets,which proved to be a teratalogical stable type of growth. Agarconcentration (0.8–1.2 per cent) in the medium influencedthe type of development, and 0.05, 1 or 2 mg l^–1 of NAAin the medium did not change the results. The succulent plantletsdid not revert to normal growth when transferred to medium containingmore agar, which favoured normal plantlet development. Succulentexcised meristems developed mainly into succulent plantlets. A hypothesis is made that a rearrangement of the meristem occursin the first days of growth, the consequence of which is thesucculent plantlet, which is no longer influenced by agar concentrationin the medium. Carnation, Dianthus caryophyllus L. cv. Cerise Royalette, vegetative shoot meristem, agar effect, meristem organization     

Leaf and Tiller Production of Prairie Grass (Bromus willdenowii Kunth) and Two Ryegrass (Lolium) Species

A detailed morphological study of three prairie grass cultivars(Bromus willdenowii Kunth) was conducted under ‘vegetative’and ‘reproductive’ growth conditions (short andlong photoperiods) and at different temperatures. Perennialryegrass (Lolium perenne L.) and Westerwolds ryegrass (Loliummuhiflorum Lam.) were compared during vegetative growth. Prairie grass had higher leaf appearance rates (leaves per tillerper day) and lower site filling (tillers per tiller per leafappearance interval) than the ryegrass species. Tillering rates(tillers per tiller per day) were also lower, except under vegetativeconditions at 4C. Low tiller number in prairie grass was notdue to lack of tiller sites but a result of poor filling ofthese sites. Lower site filling occurred because of increaseddelays in appearance of the youngest axillary tiller and lackof axillary tillers emerging from basal tiller buds. In prairiegrass, no tillers came from coleoptile buds while only occasionallydid prophyll buds develop tillers. Low tiller number in prairiegrass was compensated for by greater tiller weight. Prairiegrass had more live leaves per tiller, greater area per leafand a high leaf area per plant. Considerable variation between cultivars was found in prairiegrass. The cultivar ‘Bellegarde’ had high leaf appearance,large leaves and rapid reproductive development, but had lowlevels of site filling, tillering rate, final tiller numberand herbage quality during reproductive growth. ‘Primabel’tended to have the opposite levels for these parameters, while‘Grasslands Matua’ was intermediate and possiblyprovided the best balance of all plant parameters. prairie grass, Bromus willdenowii Kunth, perennial ryegrass, Lolium perenne L., Westerwolds ryegrass, Lolium multiflorum Lam., temperature, photoperiod, leaf appearance, leaf area, tillering, site filling, tillering sites, yield     

Determinate Floral Buds of Plantain (Musa AAB) as a Site of Adventitious Shoot Formation

Floral buds of the ‘False Horn’ plantain clonesMusa (AAB) ‘Harton Verde’, ‘Harton Negra’,and ‘Currare’ terminate in a large single floralstructure. The apices of these floral buds are here designatedas determinate since they have lost the ability to produce additionalfloral initials or buds. Terminal peduncle segments can be culturedin a modified Murashige and Skoog (1962) medium supplementedwith N⁶-benzyl-aminopurine (5 mg I^–1). Under these conditions,this apparent inability to yield buds can be overcome as vegetativeshoot clusters form in the axils of the bracts. Rooted plantletsare obtainable by treating shoots with naphthaleneacetic acid(1 mg I^–1) and activated charcoal (0.025%). The adventitiousorigin of the shoots has been established. Musa cultivars, plantains, floral bud, adventitious buds, tissue culture     

Narrow-leafed Lupins with Restricted Branching

Crop phenology is one of the most important characters influencingproductivity in a given environment. Narrow-leafed lupin (Lupinusangustifolius L.) is a major grain legume crop in southern Australiawith general phenological adaptation to this Mediterranean-typeenvironment. However, it is an indeterminate crop with severalassociated limitations to productivity, such as overlappingvegetative and reproductive growth, late grain filling and sometimesexcessive vegetative growth. Here we studied two novel typesof narrow-leafed lupin with restricted branching, which mightbe useful for overcoming these problems. These restricted branchinglupins arose spontaneously within a breeding population, inthe case of ‘Tallerack’, and within a farmer's cropin the case of ‘ Hurst’ and we compared them withthe ‘Merrit’, which is widely grown and has thenormal indeterminate branching habit. The morphology and developmentof the main shoot of these genotypes were similar. However,‘Hurst’ had much larger leaves. There were alsostriking differences in the lateral branches of the restrictedbranching types; they had fewer leaves than ‘Merrit’and flowered earlier. These differences were most marked in‘ Hurst’, where the upper main stem branches werereduced to a single floret in the axil of main stem leaves,and these flowers often exhibited abnormal morphology. Copyright2000 Annals of Botany Company Lupinus angustifolius L., narrow-leafed lupin, adaptation, development, morphology, branching, leaves, mutant, plastochron, phyllochron, floral initiation, flowering.     

A COMPARATIVE DEVELOPMENTAL STUDY OF THE MUTANT SIDESHOOTLESS AND NORMAL TOMATO PLANTS

'Sideshootless,’ a mutant strain of tomato which does not produce axillary buds during vegetative growth, was compared with normally branching plants in order to study the nature of development particularly with regard to axillary buds. Sectioned material revealed no indication of axillary bud initiation in the sideshootless plant at any time during the vegetative phase of growth. In the normal plants, buds were noted to arise in the axil of the fifth youngest leaf. The buds take their origin in tissue which is in direct continuity with the apical meristem. The bud primordia later become set apart from the apex as vacuolation takes place in the surrounding tissue. At the time of floral initiation, the mutant and normal strains behave similarly. Axillary buds appear in the axils of the 2 leaves immediately below the floral apex. One of the buds elongates to overtop the existing plant axis; the other develops as a typical sidebranch. The inflorescence is pushed aside in the process. This pattern is repeated with each inflorescence; thus an axis composed of several superimposed laterals results.     

Physiology of Flowering in Saccharum: I. DAYLENGTH CONTROL OF FLORAL INITIATION AND DEVELOPMENT IN S. SPONTANEUM L.

Flowering in two clones of Saccharum spontaneum L. is controlledby photoperiod. The earliest stages of development, ‘induction’and ‘initiation of the inflorescence axis primordium’(IAP) were optimally promoted under intermediate days of 12h 30 min, while the subsequent stage ‘initiation of inflorescencebranch primordia’ (IBP) was inhibited by days longer than13 h. The following stage ‘initiation of spikelet primordia’(ISP) showed a quantitatively intermediate response with anoptimum photoperiod of 9 h to 11 h. The elongation of the differentiatedinflorescence was found to be only slightly sensitive to photoperiodsof 13 h or longer in one of the clones. Unfavourable photoperiodsat stages following induction resulted in the arrest or delayof inflorescence development and when these were given duringthe IAP and IBP stages, reversion to the vegetative conditioncommonly occurred.     

Floral activity in solutions of deoxyribonucleic Acid extracted from tobacco stems

For Nicotiana tabacum cv. Wis. 38 plants, the capabilities of solutions containing DNA, extracted from either homogenates of stems in a floral state or nuclei of stems in a vegetative state, to effect flowering of vegetative plants have been studied. Previous work indicates that the DNA from homogenates of stems in a floral state is mainly nuclear. If DNA solutions are supplied to axillary buds of vegetative plants and if the axillary buds are defoliated every 4th day for 12 days, the buds supplied a solution of DNA from stems in a floral state initiate flowers under noninductive conditions, and the buds supplied a solution of DNA from stems in a vegetative state remain vegetative. Heating and rapidly cooling a solution of DNA from stems in a floral state enhances its floral activity. Heating and cooling a DNA solution also results in novel flowers showing up in many treated plants. Novel flowers are more striking in the offspring than in the parents. The capabilities of heated-cooled DNA solution to initiate flowers in noninductive conditions and to cause novel flowers are eliminated completely by treating (before heating and cooling) the DNA solution with deoxyribonuclease. Heated-cooled solutions of DNA extracted from nuclei of either vegetative stems or vegetative leaves contain no floral activity.     

Basipetal Gradient of Axillary Bud Inhibition Along a Rose (Rosa hybridaL.) Stem: Growth Potential of Primary Buds and their Two Most Basal Secondary Buds as Affected by Position and Age

InRosa hybridaL. cv. Ruidriko ‘Vivaldi’®, theeffect of position on growth and development potentials of axillarybuds was investigated by single internode cuttings excised alongthe floral stem and its bearing shoot. The experiments werecarried out in both glasshouses and in a phytotron. The studyfirstly concerned the development of the primary shoot fromthe onset of bud growth until anthesis. The primary shoot wasthen bent horizontally to promote the growth of the two mostproximal secondary buds, the collateral buds, already differentiatedinside the primary bud. They gave rise to basal shoots. In thebasipetal direction, the axillary buds along the floral stemexhibited both an increase in the lag time before bud growthand a decrease in bud growth percentage, demonstrating the existenceof a physiological basipetal gradient of inhibition intrinsicto the buds or due to short range correlations. The same basipetalgradient of inhibition was observed along the floral stem andits bearing shoot, demonstrating that the age of the bud wasnot a major factor in determining the rate of bud growth. Afterbending the primary shoot, the percentage of collateral budgrowth was also affected by the cutting position. The more proximalthe cutting, the lower the sprouting ability of collateral buds.The growth potential of these buds appeared to be already determinedinside the main bud before cutting excision.Copyright 1998 Annalsof Botany Company Axillary bud; basal shoot; cutting; development; endodormancy; growth; paradormancy; position; primary shoot;Rosa hybridaL.; rose; secondary bud; topophysis.     

TENDRILS OF PASSIFLORA FOETIDA: HISTOGENESIS AND MORPHOLOGY

Passiflora foetida bears an unbranched tendril, one or two laterally situated flowers, and one accessory vegetative bud in the axil of each leaf. The vegetative shoot apex has a single-layered tunica and an inner corpus. The degree of stratification in the peripheral meristem, the discreteness of the central meristem, and its centric and acentric position in the shoot apex are important plastochronic features. The procambium of the lateral leaf trace is close to the site of stipule initiation. The main axillary bud differentiates at the second node below the shoot apex. Adaxial to the bud 1–3 layers of cells form a shell-zone delimiting the bud meristem from the surrounding cells. A group of cells of the bud meristem adjacent to the axis later differentiates as an accessory bud. A second accessory bud also develops from the main bud opposite the previous one. A bud complex then consists of two laterally placed accessory bud primordia and a centrally-situated tendril bud primordium. The two accessory bud primordia differentiate into floral branches. During this development the initiation of a third vegetative accessory bud occurs on the axis just above the insertion of the tendril. This accessory bud develops into a vegetative branch and does not arise from the tissue of the tendril and adjacent two floral buds. The trace of the tendril bud consists of two procambial strands. There is a single strand for the floral branch trace. The tendril primordium grows by marked meristematic activity of its apical region and general intercalary growth.     

GIBBERELLIN-INDUCED INHIBITION OF FLORAL INITIATION IN FUCHSIA

The ‘Lord Byron’ cultivar of Fuchsia hybrida is a long day plant for which GA acts as an inhibitor of flower initiation. At the dosages required to inhibit initiation (0.025 μg per plant) GA also promotes increased stem elongation but causes no other departures from normal development. Similar tests with auxins, antiauxins, kinins, and other substances showed no effect on flower initiation at dosages equivalent to that for GA. At 10- to 100-fold greater dosages, auxins, kinins, and anti-auxins inhibit not only flower initiation but also vegetative development. Thus the effect of GA on flower initiation appears to be unique, although other hormonal substances, such as abscisin, have not been tested. GA-induced inhibition is directly proportional to the dosage applied and inversely to the strength of long day induction (as measured by the number of long days). GA is most effective when applied to the terminal bud rather than to the mature leaves, suggesting that it is active at the site of flower initiation rather than in the leaves. If it is applied after translocation of the floral stimuli from the leaves, GA does not prevent flower initiation. Regardless of the dose applied, GA is less effective if applied later rather than earlier during LD induction. The inhibitory effect persists for several days. For example, an 0.85 μg dosage causes an 8–10-day delay in initiation; lower dosages have reduced effects. GA inhibits flower initiation but has no effect upon flower development. The rate of bud development is the same in GA-treated and control plants. Apparently no more than one to two axillary buds immediately below the apical meristem are receptive to long day-induced floral stimuli from the leaves. Regardless of the daylength conditions axillary buds more basal do not initiate flowers but develop into branch axes. The effect of a long day treatment persists for a very short time, perhaps no longer than the inhibition caused by minimal GA dosage. Thus flower initiation continues for a very short time following the end of long day induction. The significance of these findings is discussed in relation to the many reports of GA-induced inhibition as well as promotion of flower initiation. In particular, the discussion concerns the nation that flower initiation in fuchsia may be controlled by a gibberellin-like transmissible inhibitor.     

Photoperiodic Regulation of Flowering in Cowpeas (Vigna unguiculata (L.) Walp.)

To test the proposition that photoperiodic controls synchronizethe flowering of cowpeas, Vigna unguiculata (L.) Walp. [V. sinensis(L.) Savi], the day-length requirements for floral initiationand for flowering were investigated in several short-day accessions.No evidence was found of different critical photoperiods atdifferent stages of development, but exposure to only 2–4short days was required for floral initiation compared withabout 20 for development to open flowers. Pod setting was increasedafter exposure to even one short day more than the number requiredfor flower opening. Floral buds at higher nodes appeared to require fewer shortdays for development to flowering than buds at the lower nodes,and displayed faster rates of development. Inflorescence budsdid not resume development if they were exposed to 15 or morelong days following inflorescence initiation. Thus, any tendencytowards synchronous flowering in cowpeas is not due to the criticalday-length for flower development being shorter than that forflower initiation, but could be the result of cumulative photoperiodicinduction of plants and the more rapid development of later-formedflowers. Vigna unguiculata (L.) Walp., cowpeas, flower initiation, flower development, fruit set, photoperiodism     

Influence of Water Stress on Flowering and Seed Production of Macroptilium atropurpureum cv. Siratro

Macroptilium atropurpureum cv. Siratro was grown in large soilbeds with a constant water table below, developing a dawn leafwatêr potential of --0.25 MPa. Water stresses equivalentto -0.7 or -1.0 MPa were developed over 14 d, causing reducedstem and bud elongation, leaf expansion, and bud differentiationand survival. Apex size, the proportion of buds which were floralor vegetative, the early phases of floral initiation, and seedformation on advanced inflorescences were little affected duringthe water deficit period. Upon rewatering previously stressed plants showed increasesrelative to control plants in the rates of shoot appearance,leaf expansion and new node appearance. The ratio of buds becomingfloral was independent of watering treatment, and the enhancedrate of floral bud production in the previously-stressed treatmentswas due to higher rates of total bud differentiation which persistedfor up to six weeks after rewatering. Survival of floral budswas reduced by previous stress, but number of flowers per inflorescence,pod setting, seed number per pod and 100-seed weight were independentof treatment. Seed production was controlled by inflorescencedensity. Rate of seed production was independent of treatmentduring water deficit and four weeks subsequently, and was thenenhanced by 46 and 54 per cent relative to the control in the–0.7 and –1.0 MPa treatments respectively. Macroptilium atropurpureum, Siratro, floral initiation, flowering, seed production, water stress, bud development     

Ontogeny of Axillary and Accessory Buds in Clerodendrum phlomidis L.

Plastochronic changes in the vegetative shoot apex and originand development of axillary and accessory buds are studied. The flat shoot apex shows structural and dimensional changesin a plastochron. They are described in three phases, the pre-leafinitiation, the leaf initiation, and the post-leaf initiation.The youngest axillary bud meristem is identified near the axilat the second node when the subtending leaf primordium is 200–12µ long. The corpus of the bud meristem has a more activerole in bud development than has the tunica layers. The shellzone associated with a young bud meristem persists until thebud has attained the structural and functional attributes ofthe main shoot apex. It loses its histological identity by producingderivatives which merge with the ground tissue and procambialcells of bud traces. In a developing bud the provascular systemof the bud appears as an arc, a loop, or as a ring in transversesections at different levels. These configurations are composedof anastomosing procambial strands of bud trace and residualmeristem, both being differentiated from developing bud meristem.     

Morphology and Anatomy of Stems and Pedicels of Spring Flush Shoots Associated with Citrus Fruit Set

Flowering and vegetative shoots of ‘Shamouti’ orange[Citrus sinensis (L.) Osbeck] and ‘Marsh’ seedlessgrapefruit (Citrus paradisi Macf.) were examined for correlationof their morphology and anatomy with fruit set. Fruit set isfavoured on leafy inflorescences whereas abortion is nearlycomplete on leafless inflorescences. Leafless inflorescencesof ‘Shamouti’ with one flower were found to havea very thin stem which contained few vascular bundles, whereasthose with three flowers had better-developed vascular systems.The vascular system of leafy inflorescences is significantlydifferent from that of leafless ones and contains a distinctcentral xylem cylinder. The vascular area of leafless inflorescencesis only about one-quarter of that of the leafy ones. The vascularsystem of grapefruit resembles that of the ‘Shamouti’orange. This study emphasizes the importance of the dimensionof the vascular system for fruit set and provides a possibleexplanation for the better fruit set on both leafy and leaflessinflorescences with several flowers compared with single-floweredinflorescences. Anatomy; citrus; fruit set; leafless inflorescence; leafy inflorescence; pedicel; vascular system; vegetative shoot     

DEVELOPMENT OF FLORAL ORGANS IN THE SITES OF LEAF PRIMORDIA IN PINGUICULA VULGARIS

Plants of Pinguicula vulgaris L. have either clockwise or counterclockwise spiral phyllotaxy. The inception of floral primordia occurs in leaf sites as a normal sequence of development. Only two leaf primordia initiated late in the season develop into floral primordia in the following year. They do not represent a direct modification of the apical meristem nor of the detached meristem. The apical meristem continues to produce leaves in the vegetative phase and flowers in the reproductive phase, and thus the plants show a monopodial growth. Axillary buds are not developed in this perennial species and instead additional buds of adventitious ontogeny appear. Such buds are produced on the older leaves of larger plants, and they are extremely useful in the vegetative propagation of the species.