Nitrogen Deficiency Slows Leaf Development and Delays Flowering in Narrow-leafed Lupin

Effects of nitrogen (N) supply on leaf and flower developmentinLupinus angustifolius L. cv Merrit were examined in a temperature-controlledglasshouse. Low N supply (0.05 or 0.4 mM N) had little effecton leaf initiation but slowed leaf emergence on the main stemcompared with plants receiving high N supply (6.0 or 6.4 mMN), or with symbiotic N₂-fixation. Plants experiencing transientN deficiency had slower leaf emergence than plants with a continuoussupply of 6.4 mM N. Nitrogen supply did not affect the timeof floral initiation, which occurred within 4 weeks of sowing,by which time nine to ten leaves had emerged. However, the floweringof low-N plants was delayed by 68 to 220 °C d (i.e. 4–14d) even though they had fewer leaves. The effect of N deficiencyon flowering time was largely a result of slower leaf emergence. Lupinus angustifolius L.; nitrogen; leaf; flower initiation; thermal time; plastochron; phyllochron     

FLOWER INITIATION IN TOTAL DARKNESS IN A QUANTITATIVE SHORT DAY PLANT, FAGOPYRUM ESCULENTUM MOENCH

The flowering behavior of two cultural varieties of Fagopyrumesculentum Moench aseptically cultured in total darkness wasstudied. The effect on the flower initiation of some chemicalsubstances added to sterilized dry seeds was also investigated.Low temperature was found to be more suitable for flower initiationin buckwheat plants. 2-Thiouracil promoted flower initiationat high temperature in total darkness and inhibited it at anytemperatures examined under light conditions. Sucrose promotedflower initiation at higher temperatures than 15. Lithium chlorideand peptone inhibited flower initiation only at high temperature.Indoleacetic acid, gibberellin and kinetin had no effect onflower initiation in total darkness. It is postulated that in the flowering response the primaryreaction may be connected with the metabolism of sucrose andribonucleic acid. (Received September 21, 1964; )     

Inhibition imposed by developing flowers on further flower-bud initiation in Chamelaucium uncinatum Schau

In Chamelaucium uncinatum, an Australian woody perennial, flower initiation ceases under continuous inductive short-day (SD) conditions after the first flowering flush. The developing flowers were found to be the prime cause of the cessation in flower initiation. Removal of flowering shoots or lowers as soon as the buds appeared resulted in continuous flower formation. Pruning the plants below the young flower buds at the same stage also caused increased flower formation at the tips of the new growth. If pruning was delayed until flower buds were approx. 3 mm in diameter, however, nor further flower initiation took place and the plants, although still under inductive conditions, shifted to vegetative growth. The inhibiting factor is translocated from one branch to another. At least a six-week rest period (a vegetative growth period under long-day conditions) is needed before the plants are able to respond to further SD stimuli.Abbreviations LD long day - SD short day - SE standard error     

FLOWERING OF DICHONDRA IN RESPONSE TO TEMPERATURE AND DAYLENGTH

Experiments using controlled environment facilities showed that flowering of Dichondra repens was promoted by chilling plants at 10 C or below. Optimum length of the chilling period was 5–6 weeks. Unchilled plants did not flower. The flowering stimulus resulting from chilling was destroyed by temperatures above 21 C. Rate of flowering was increased by short days during chilling, but short days could not substitute for the chilling requirement. Optimum daylength for flower initiation following chilling was approximately 14 hr and the optimum temperature was approximately 15 C. Flower buds developed in leaf axils of primary stems and laterals, but stem apices remained vegetative. When the chilling requirement was met flowering continued indefinitely as the plants grew.     

31种木本植物开花物候与系统发育的关系

植物物候通常被认为是由环境因素,如降水、温度和日照长度所决定,然而环境因素是否是物候唯一的决定因素仍然存在很大争议。谱系结构表征了植物在进化上的顺序,该发育时序是否对物候产生影响,当前仍然未知。在调查2016年春季新疆乌鲁木齐市最常见的31种木本植物的初始开花时间、败花时间和开花持续时间的基础上,通过分析植物开花物候的分布特征、开花物候在乔灌木间的差别、以及植物谱系距离与开花物候距离间的关系,试图揭示植物的开花物候和物种谱系(进化)顺序间的关系。结果表明:(1)新疆乌鲁木齐市31种木本植物的初始开花时间为4月18日±9d、败花时间为5月5日±12d、开花持续时间为(16±8)d;(2)乔木的初始开花时间和败花时间的标准差分别均低于灌木,乔木开花物候相对灌木更稳定;(3)乔木的初始开花和败花时间均显著早于灌木(P0.05),但开花持续时间在两者间未有显著性差异(P0.05);(3)31种木本植物间的初始开花时间距离、败花时间距离和开花持续时间距离均与物种谱系距离存在显著线性回归关系(P0.05)。综上可知:乔灌木在垂直空间上的分化使得木本植物的开花物候在植物生活型间存在不同。对植物的开花物候,除已被证明的降水、温度和日照长度等环境因素的影响外,物种进化顺序也可能造成了它在植物种间、时间和空间上的变异。     

Rainfall and flowering synchrony in a tropical shrub: Variable selection on the flowering time ofErythroxylum havanense

Summary We tested the adaptive significance of flowering synchrony by means of a quantitative analysis of selection and by flowering induction experiments with the deciduous shrubErythroxylum havanense. Temporal schedules of flower and fruit production were determined for a local population (in three sites) in a Mexican seasonal forest for 2 years (1987–1988). The consequences of natural variation in flowering time (flowering initiation day) on maternal reproductive success (fecundity) were evaluated. We observed high levels of inter- and intraindividual flowering synchrony in 1987, but not in 1988 and this contrast was related to differences in rainfall patterns between the two years. A significant proportion (15.4%) of the phenotypic variation in flowering initiation day was accounted for by environmental variance. The expression of phenotypic variance of flowering time and, consequently, the opportunity for selection to act, are controlled by annual variation in rainfall. Despite the between-year difference in flowering synchrony, we detected a relatively intense directional selection on flowering initiation day in both years, but selection coefficients were of opposite sign (standardized directional gradients were –0.326 and 0.333 for 1987 and 1988, respectively). For both years there was a significant relationship between individual relative fitness and the number of neighbouring flowering plants in a given day, suggesting positive frequency-dependent selection.     

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     

METABOLISM AND FLOWERING

Two earlier papers have established (1) that the late-flowering chrysanthemum, a typical "short-day" species, flowered in autumn because of a disability in nocturnal translocation which limited the amount of carbohydrate available at the growing-point during the short nights of summer (Grainger, 1938), and (2) that many plants which flower in spring and early summer actually begin the formation of their flower initials in the autumn and winter of the previous year (Grainger, 1939). Such plants might conceivably be "short-day" kinds, since the actual transformation from vegetative to floral organization of the growing-point was accomplished when the days were short. It therefore appears necessary to investigate their relative diurnal carbohydrate metabolism, in order to discover whether it has any causal relationship with the time of actual flower initiation, as was demonstrated for the late-flowering chrysanthemum. The present paper describes the results of such an investigation, and also of certain contributory studies as to the converse effect of flowering upon metabolism, the relative amount of energy used in flowering, and the possible inadequacy of nutrition in very floriferous plants.     

Inhibition of growth and synchronised cell division in the shoot apex in relation to flowering in Silene

When plants of Silene coeli-rosa (L.) Godron were induced by seven long days, then exposed to darkness for 48 h before being returned to short days, they went on to initiate flowers with a delay of about 2 d. The synchronisation of cell division which normally occurs before flower initiation was suppressed, showing that it is not essential for flowering. Periods of darkness of up to 240 h inhibited apical growth and leaf initiation but did not prevent eventual flowering in short days. The commitment of the apex to flower was therefore maintained while apical growth was inhibited.Abbreviations SD short day(s) - LD long day(s)     

Ectopic expression of an orchid (Oncidium Gower Ramsey) AGL6-like gene promotes flowering by activating flowering time genes in Arabidopsis thaliana

An AP1/AGL9 group of MADS box gene, OMADS1, with extensive homology to the Arabidopsis AGAMOUS-like 6 gene (AGL6) was characterized from orchid (Oncidium Gower Ramsey). OMADS1 mRNA was detected in apical meristem and in the lip and carpel of flower. Yeast two-hybrid analysis indicated that OMADS1 is able to strongly interact with OMADS3, a TM6-like protein that was involved in flower formation and floral initiation in orchid. Transgenic Arabidopsis and tobacco ectopically expressed OMADS1 showed similar novel phenotypes by significantly reducing plant size, flowering extremely early, and losing inflorescence indeterminacy. In addition, homeotic conversion of sepals into carpel-like structures and petals into staminoid structures were also observed in flowers of 35S::OMADS1 Arabidopsis. This result indicated that OMADS1 was involved in floral formation and initiation in transgenic plants. Further analysis indicated that the expression of flowering time genes FT, SUPPRESSOR OF OVEREXPRESSION OF CO 1 (SOC1) and flower meristem identity genes LEAFY (LFY), APETALA1 (AP1) was significantly up-regulated in 35S::OMADS1 transgenic Arabidopsis plants. Furthermore, ectopic expression of OMADS1 rescued late-flowering phenotype in gi-1, co-3 but not for ft-1 and fwa-1 mutants. These results supported that ectopic expression of OMADS1 influenced flower transition and formation by acting as an activator for FT and SOC1 in Arabidopsis.     

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.     

Growth schedule of Xanthium canadense: Does it optimize the timing of reproduction?

Summary The effects of nutrition on the timing of reproductive initiation of a short-day annual plant Xanthium canadense (cocklebur) were examined with the following hypotheses in mind: If the plant always follows an optimal growth schedule, low-nutrient plants will initiate reproductive growth earlier than high-nutrient plants. On the other hand, if the plant flowers in response to photoperiodic stimuli, both plants will initiate reproductive growth on the same day. The sand-culture experiment showed that high-nutrient plants flowered earlier than the low-nutrient plants, leading to rejection of the first hypothesis. The predicted optimal flowering time is 2 days later than the actual flowering time in high-nutrient plants and 10 days earlier in low-nutrient plants. These deviations from the optimal times reduced the reproductive yield by 0.1% and 2.3%, respectively. The ratio of the final reproductive yield to the vegetative mass at flower initiation was 1.10 in high-nutrient plants and 0.63 in low-nutrient plants. Since the expected ratio for the optimal growth schedule is 1.0, high-nutrient plants followed the opitmal growth schedule more closely than the low-nutrient plants. Cocklebur is a fast-growing annual which is common in relatively nutrient-rich environments. This study suggests that cocklebur adapts itself to such environments through its photoperiodic response.     

Temperature during the day, but not during the night, controls flowering of Phalaenopsis orchids

Phalaenopsis orchids are among the most valuable potted flowering crops commercially produced throughout the world because of their long flower life and ease of crop scheduling to meet specific market dates. During commercial production, Phalaenopsis are usually grown at an air temperature > or =28 degrees C to inhibit flower initiation, and a cooler night than day temperature regimen (e.g. 25/20 degrees C day/night) is used to induce flowering. However, the specific effect of day and night temperature on flower initiation has not been well described, and the reported requirement for a diurnal temperature fluctuation to elicit flowering is unclear. Two Phalaenopsis clones were grown in glass greenhouse compartments with constant temperature set points of 14, 17, 20, 23, 26, or 29 degrees C and fluctuating day/night (12 h/12 h) temperatures of 20/14, 23/17, 26/14, 26/20, 29/17, or 29/23 degrees C. The photoperiod was 12 h, and the maximum irradiance was controlled to < or =150 micromol m(-2) s(-1). After 20 weeks, > or =80% of plants of both clones had a visible inflorescence when grown at constant 14, 17, 20, or 23 degrees C and at fluctuating day/night temperatures of 20/14 degrees C or 23/17 degrees C. None of the plants were reproductive within 20 weeks when grown at a constant 29 degrees C or at 29/17 degrees C or 29/23 degrees C day/night temperature regimens. The number of inflorescences per plant and the number of flower buds on the first inflorescence were greatest when the average daily temperature was 14 degrees C or 17 degrees C. These results indicate that a day/night fluctuation in temperature is not required for inflorescence initiation in these two Phalaenopsis clones. Furthermore, the inhibition of flowering when the day temperature was 29 degrees C and the night temperature was 17 degrees C or 23 degrees C suggests that a warm day temperature inhibits flower initiation in Phalaenopsis.     

Arbuscular mycorrhizal fungi differ in affecting the flowering of a host plant under two soil phosphorus conditions

Aims Studies have showed that arbuscular mycorrhizal fungi (AMF) can greatly promote the growth of host plants, but how AMF affect flowering phenology of host plants is not well known. Here, we conducted a pot experiment to test whether life cycle and flowering phenology traits of host plant Medicago truncatula Gaertn can be altered by AMF under low and high soil phosphorus (P) levels.Methods The experiment was conducted in a greenhouse at Zhejiang University in China (120°19′E, 30°26′N) and had a completely randomized design with two factors: AMF treatments and soil P levels. Six AMF species (Acaulospora scrobiculata, As; Gigaspora margarita, Gma; Funneliformis geosporum, Fg; Rhizophagus intraradices, Ri; Funneliformis mosseae, Fmo and Glomus tortuosum, Gt.) were used, and two soil P levels (24.0 and 5.7 mg kg^-1 Olsen-soluble P) were designed. The six AMF species were separately inoculated or in a mixture (Mix), and a non-AMF control (NAMF) was included. When plants began to flower, the number of flowers in each pot was recorded daily. During fruit ripening, the number of mature fruits was also recorded daily. After ~4 months, the biomass, biomass P content and AMF colonization of host plant were measured. Correlation between root colonization and first flowering time, or P content and first flowering time was analyzed.Important findings Under the low P level, first flowering time negatively correlated with root colonization and biomass P. Only host plants with AMF species As, Fg, Ri, or Mix were able to complete their life cycle within 112 days after sowing. And treatment with AMF species Fg, Gt, or As resulted in two periods of rapid flower production while other fungi treatments resulted in only one within 112 days after sowing. The cumulative number of flowers produced and biomass P content were highest with species Fg. Host biomass allocation significantly differed depending on the species of AMF. Under both soil P levels, the host plant tended to allocate more biomass to fruits in the Mix treatment than in the other treatments. These results indicated that the effects of AMF on host flowering phenology and biomass allocation differed depending on AMF species and soil P levels.     

The transition to reproductive phase inchenopodium murale L. ecotype 197 - Early flowering long-day plant

Five days of suitable continuous light induced flowering in the majority ofChenopodium murale L. ecotype 197 plants as early as at the phase of the first pair of leaves. At the time of initiation of the 2nd to 4th pairs of leaves the capacity of plants to flower was reduced, the number of flowering plants being significantly lower under the same inductive light treatment. The capacity to flower increased again at the phase of the 5th and the 6th pairs of leaves. Inductive light treatment brought about a marked growth activation of organs present before induction, shoot apex elongation, precocious formation of new leaves and activation of axillary meristems. The course of these changes in plants of different age is demonstrated. The terminal flower developed during 5 short days following inductive light treatment. The paper shows similarities and differences between long-daymutale L. ecotype 197 and short-day C.rubrum L. ecotype 374 grown under practically uniform conditions.     

EXPERIMENTS ON THE PHOTOPERIODIC RESPONSE IN PINEAPPLE

Gowing , Donald P. (Pineapple Research Institute of Hawaii, Honolulu.) Experiments on the photoperiodic response in pineapple. Amer. Jour. Bot. 48(1): 16–21. 1961.—The initiation of flowering of ‘Smooth Cayenne’ pineapple plants is neither strictly a response to photoperiod (day lengths of 10 hr. 51 min.–13 hr. 24 min.) nor to a minimum temperature (minima from 50° to 72°F. in different areas) under natural Hawaiian conditions. Depending on the kind of planting material used and the time of planting, natural initiation of flowering may take place any month of the year. Slips planted in the fall generally initiate flowering in December of the following year. However, exposure of an 8-mo.-old slip-planting to a day length of 8 hours for 40 days starting Sept. 8 induced flowering irrespective of night temperatures from about 60 to 80°F. Interruption of the dark period by illumination at 30 ft.-c. from midnight to 1 a.m. suppressed the inductive effect. Lowering the night temperature to 60°F. was, of itself, non-inductive. Field-grown, 11-mo.-old plants treated in place responded similarly, in that 25 periods of 8-hr. day length starting Sept. 5 induced 60% of the plants to flower, and the night illumination suppressed the inductive effect as before. Daily application of 0.12 mg. of the major native pineapple auxin (indole-3-acetic acid) at the beginning of the dark period had no detectable effect on the short-day treatment, and similar application of an antiauxin (4-chlorophenoxyisobutyric acid) did not affect the suppression of flowering by the light-break. Supplemental illumination of field-grown 12-mo. plants to provide a photoperiod of more than 15 hr. daily from Nov. 4 to Jan. 30 did not suppress the natural initiation of flowering which occurred in early December (day length about 10 hr. 50 min.). ‘Smooth Cayenne’ pineapple is therefore a quantitative, but not an obligate, short-day plant.     

The influence of pre-floral growth and development on the pathway of floral development, dry matter distribution and seed yield in oilseed rape (Brassica napus L.)

Patterns of floral development, dry matter distribution and seed yield were examined in winter oilseed rape plants subjected to different pre-floral growth environments. The duration of pre-floral growth and plant size at flower initiation, measured in terms of total mainstem leaf number, were manipulated by varying the temperature between seedling emergence and flower initiation. Exposure of seedlings to low temperatures from cotyledon expansion onwards markedly reduced the duration of pre-floral growth and the number of leaves on the mainstem. The subsequent development pattern of plants was largely dependent on the date of flower initiation and therefore vernalisation requirement. Indeed, the period of growth from flower initiation to maturity, considered on the basis of thermal time, was directly related to the duration of pre-floral growth and mainstem leaf number. The thermal durations of the bud development phase and flowering period in plants exposed to different pre-floral cold treatments but with a common date of flower initiation were similarly linked to these two parameters. Plants exposed to prolonged periods of low temperature treatment from cotyledon expansion onwards initiated fewer mainstem leaves during a relatively short pre-floral growth phase and their yield potential was limited by a reduction in branch and flower numbers. Plants maintained at higher temperatures produced more mainstem leaves during an extended period of pre-floral growth and supported a greater number of branches and flowers. However, this additional yield potential was not realised due to a reduction in seed numbers and mean seed weight. It appeared that seed yield of these plants was limited by increased competition between an excessive number of lower branches and flowers, a problem apparently created by excessive pre-floral growth. Minimal competition for available assimilates between the limited number of branches of plants with a shorter pre-floral growth phase and fewer mainstem leaves, resulted in lower levels of pod abortion, greater seed production and ultimately increased seed yields.     

Floral initiation in strawberry: Spectral evidence for the regulation of flowering by long-day inhibition

Summary Floral initiation in strawberry cv. Cambridge Favourite, a facultative short-day plant, was inhibited by a daylength extension with red light (R) during the second half of a 16-hour night but not during the first half, and by far-red light (FR) in the first half but not during the second. Mixed R plus FR light was inhibitory to flowering at both times. This change in sensitivity to R and FR light in the evening and morning resembles the pattern for flower induction in long-day plants but differs from the pattern for flower inhibition in several other short-day plants, examples of which are given. These experiments afford further support for the hypothesis that the control of flower initiation in strawberry depends on the production of a flower inhibitor by leaves exposed to long photoperiods.Abbreviations R red - FR far-red - SD short day - LD long day - SDP short-day plant - LDP long-day plant     

Impact of enhanced ultraviolet-B radiation on flower, pollen, and nectar production

Intensified ultraviolet-B radiation or UV-B (wavelengths between 280 and 320 nm) can delay flowering and diminish lifetime flower production in a few plants. Here we studied the effects of enhanced UV-B on floral traits crucial to pollination and pollinator reproduction. We observed simultaneous flowering responses of a new crop plant, Limnanthes alba (Limnathaceae), and a wildflower, Phacelia campanularia (Hydrophyllaceae), to five lifetime UV-B dosages ranging between 2.74 and 15.93 kJ·m·d. Floral traits known to link plant pollination with bee host preference, host fidelity and larval development were measured. Intensified UV-B had no overall effect on nectar and pollen production of L. alba and P. campanularia flowers. A quadratic relationship between UV-B and nectar sugar production occurred in P. campanularia and showed that even subambient UV-B dosages can be deleterious for a floral trait. Other floral responses to UV-B were more dramatic and idiosyncratic. As UV-B dosage increased, L. alba plants were less likely to flower, but suffered no delays in flowering or reductions to lifetime flower production for those that did flower. Conversely, an equal proportion of P. campanularia plants flowered under all UV-B treatments, but these same plants experienced delayed onset to bloom and produced fewer flowers at greater UV-B intensities. Therefore, intensified UV-B elicits idiosyncratic responses in flowering phenology and flower production from these two annual plants. Diurnal patterns in nectar and pollen production strongly coincided with fluctuating humidity and only weakly with UV-B dosage. Overall, our results indicated that intensified UV-B can alter some flowering traits that impinge upon plant competition for pollinator services, as well as plant and pollinator reproductive success.     

Flowering in the uniflora mutant of tomato (Lycopersicon esculentum Mill.): description of the reproductive structure and manipulation of flowering time

The uniflora (uf) mutant of tomato (Lycopersicon esculentum Mill.) is known to produce solitary, normal, fertile flowers instead of inflorescences. Histological and SEM studies revealed that this unusual reproductive structure resulted from the inability of the plant to produce an inflorescence and not from post-initiation abortion processes affecting young flower buds. Development prior to floral transition was apparently not affected by the mutation since rates of germination and leaf initiation were identical in both uf and the Ailsa Craig (AC) initial cultivar. However, the time of flowering of the mutant was always delayed as compared to AC. In uf, environmental conditions markedly influenced flowering time which occurred early in all individuals in summer, but was strongly delayed during winter, with less than 20% plants reaching flowering before having initiated 40 leaves. Defoliation treatments stimulated floral transition in uf plants since 100% flowering occurred whatever the season and since the time of floral transition was usually advanced in comparison to the non-defoliated control plants. Similarly, compared to intact uf plants, flowering of terminal meristem of cuttings and upper axillary bud of decapitated plants was promoted. The involvement of correlative influences and assimilate availability in the control of flowering in tomato is suggested by these findings.