Effects of photoperiod in growth cabinets on the growth of leaves and tillers in three perennial grasses

Long photoperiods provided in growth cabinets and consisting of a conventional extended photoperiod or of a ‘light-break’ in the middle of a long, dark period, generally increased leaf length and sometimes leaf width and consequently the rate of expansion of leaf surface, but decreased rate of leaf production and tillering in vegetative plants of S.₃₇ cocksfoot (Dactylis glomerata L.), S.₂₁₅ meadow fescue (Festuca pratensis Huds.) and S.₂₄ perennial rye-grass (Lolium perenne L.) compared with short photoperiods. All plants received the same total amount of light each day. These effects were observed both in single plants and in plants grown close together to simulate sward conditions. The total dry weight of plant material was greater in long than in short photoperiods.     

The effect of short-term daily temperature drops on the processes of organogenesis in <Emphasis Type="Italic">Cucumis sativus</Emphasis> L. under different photoperiods

The effect of nightly temperature drops of different durations (2, 4, and 6 h) on the processes of apical and axillary meristem organogenesis was studied in young Cucumis sativus L. under short photoperiod (day/night, 10/14 h), long photoperiod (16/8 h), and continuous light. Nightly temperature drops for 2 h had no effect on cucumber development under all studied photoperiods; however, longer temperature drops (4–6 h) accelerated the development under long photoperiod and continuous light. Short-term exposures to low temperature under continuous light considerably increased lateral branching of cucumber plants.     

Growth and Development of Radish (Raphanus sativus, L.) Under Selected Light Environments

Plants of radish (Raphanus sativus L.) were grown under selectedlight conditions in controlled environmental chambers in orderto monitor the role of photoperiod, irradiance level and inputlight energy in plant development. Results indicated that thedaily input of light energy was the most important light factoraffecting leaf development while photoperiod and irradiancelevel had the major influences on storage organ development.Distribution of assimilates to leaves and storage organs variedunder different light regimes with long photoperiods and highirradiances producing the largest storage organs. Once initiated,the rate of storage organ growth was similar under all testedlight environments. Raphanus sativus L., radish, growth, development, light, photoperiod, assimilate distribution, storage organ     

Photothermal model of plant development

The development of plants depends on the photoperiod length, light intensity, temperature, and length of light day integral. The reaction of a plant to the day length or daily light integral can depend on both the range of studied light intensities and photoperiod. Based on the data concerning the effects of light and thermal integrals on the developmental rate of plants of different photoperiodic groups, a photothermal model of plant development was proposed. The model was used to calculate the lengths of optimal photoperiods and ranges of daily temperature gradients ensuring the highest developmental rate of some plants, such as soybean, wheat, cucumber, and barley.     

Photothermal model of plant development

The development of plants depends on the photoperiod length, light intensity, temperature, and length of light day integral. The reaction of a plant to the day length or daily light integral can depend on both the range of studied light intensities and photoperiod. Based on the data concerning the effects of light and thermal integrals on the developmental rate of plants of different photoperiodic groups, a photothermal model of plant development was proposed. The model was used to calculate the lengths of optimal photoperiods and ranges of daily temperature gradients ensuring the highest developmental rate of some plants, such as soybean, wheat, cucumber, and barley.     

Kinetics and time dependence of the effect of far red light on the photoperiodic induction of flowering in wintex barley

Flowering in the long day plant Hordeum vulgare L. var. Wintex barley was enhanced by the addition of far red light to the main light portion of the photoperiod. Far red energy was provided to produce quantum flux ratios (660/730 nm) and phytochrome photoequilibria (Pfr/total phytochrome) equivalent to those reported both beneath a leaf canopy and outside a canopy at twilight. The photoperiodic requirement for long days can be completely eliminated by the addition of far red light. However, both the effect of extending the photoperiod without far red and the addition of far red to 12-hour photoperiods were suboptimal. Maximal stimulation was achieved only when far red was added to continuous light. The duration of the period of maximal apex elongation rate, as well as the reduction of the time required for floral initiation, were saturated by three inductive cycles. When far red energy was provided intermittently during 3 days of continuous light, the ability to respond varied in a circadian manner. This enhancement of flowering by far red appears to be mediated by the “high irradiance response” of phytochrome.     

Influence of changes in daylength and carbon dioxide on the growth of potato

Potatoes (Solanum tuberosum L.) are highly productive in mid- to high-latitude areas where photoperiods change significantly throughout the growing season. To study the effects of changes in photoperiod on growth and tuber development of potato cv. Denali, plants were grown for 112 d with 400 micromol m-2 s-1 photosynthetic photon flux (PPF) under a 12-h photoperiod (short days, SD), a 24-h photoperiod (long days, LD), and combinations where plants were moved between the two photoperiods 28, 56, or 84 d after planting. Plants given LD throughout growth received the greatest total daily PPF and produced the greatest tuber yields. At similar levels of total PPF, plants given SD followed by LD yielded greater tuber dry mass (DM) than plants given LD followed by SD. Stem DM per plant, leaf DM, and total plant DM all increased with an increasing proportion of LD and increasing daily PPF, regardless of the daylength sequence. When studies were repeated, but at an enriched (1000 micromol mol-1) CO2 concentration, overall growth trends were similar, with high CO2 resulting in greater stem length, stem DM, leaf DM, and total plant DM; but high CO2 did not increase tuber DM.     

Influence of Photoperiod and Leaf Age on Crassulacean Acid Metabolism in Portulacaria afra (L.) Jacq

The possibility that Crassulacean acid metabolism (CAM) is subject to long day photoperiodic control in Portulacaria afra (L.) Jacq., a facultative CAM plant, was studied. Periodic measurements of ¹⁴CO₂ uptake, stomatal resistance, and titratable acidity were made on plants exposed to long and short day photoperiods. Results indicates that waterstressed P. afra had primarily nocturnal CO₂ uptake, daytime stomatal closure, and a large diurnal acid fluctuation in either photoperiod. Mature leaf tissue from nonstressed plants under long days exhibited a moderate diurnal acid fluctuation and midday stomatal closure. Under short days, there was a reduced diurnal acid fluctuation in mature leaf tissue. Young leaf tissue taken from nonstressed plants did not utilize the CAM pathway under either photoperiod as indicated by daytime CO₂ uptake, lack of diurnal acid fluctuation, and incomplete daytime stomatal closure.

The induction of CAM in P. afra appears to be related to the water status of the plant and the age of the leaf tissue. The photosynthetic metabolism of mature leaves may be partly under the control of water stress and of photoperiod, where CAM is favored under long days.

     

The Dynamics of Carbon Supply from Leaves of Barley Plants Grown in Long or Short Days

The role of the mature leaf in supplying carbon for growth inother parts of the plant was examined using a steady-rate ¹⁴CO₂labelling technique. The pattern of events occurring in theleaf during one complete 24 h cycle was compared in plants grownin, and adapted to long and short photoperiods. The rates ofleaf photosynthesis, night respiration and daytime loss of carbonfrom the growing regions of the plant Were similar in long orshort photoperiods. As a percentage of the total carbon fixedduring the photoperiod, total respiration was c. 50% for shortday plants but only 25% for long day plants. Thirty to forty per cent of the carbon fixed during the photoperiodwas retained in the leaf for export during darkness—therest was exported immediately. In leaves of short day plantssucrose and starch were the main form of the stored carbon.By the end of the dark period these compounds had been almostcompletely depleted. In leaves of long day plants there weremuch larger basal levels of sucrose and starch, upon which thediurnal variations were superimposed. These leaves also accumulatedfructosans. The delay in starch remobilization previously foundin leaves of short day plants was also evident in leaves oflong day plants even though large concentrations of sucroseand fructosans were present This suggests the presence of distinctpools of sucrose in the leaf.     

Are cuttings suitable for assessing maturity type in potato (Solanum tuberosum)?

Two experiments were carried out to evaluate the potential of single‐node cuttings of potato (Solanum tuberosum) as a tool to assess genotypic differences in maturity type. Plants were exposed to different photoperiodic treatments (different photoperiods, different numbers of photoperiodic cycles), and cuttings were taken at different plant ages. Cuttings from early (and to a lesser extent also late) maturing varieties exposed to short photoperiods showed strong induction to tuberise, irrespective of plant age; the induction increased with an increase in the number of short photoperiodic cycles. The response of cuttings taken from early‐maturing varieties exposed to long photoperiods depended on plant age: cuttings showed stronger induction when mother plants were older; cuttings from late‐maturing varieties hardly tuberised after exposure to long photoperiods. The tuberisation of the cuttings did not depend on the length of the long photoperiod (18 or 24 h) or on the number of cycles of a photoperiod of 18 h. Tuberisation on cuttings did not properly reflect the tuber formation on the mother plants, although within varieties, significant correlations between tuberisation on cuttings and tuber yield per plant 9 weeks after planting were found with different numbers of photoperiodic cycles of 12 h. Our experiments show that the cutting technique cannot be used on older plants to assess the maturity type of potato varieties, as there are interactions between photoperiod, genotype, plant age and number of photoperiodic cycles, in the reflection of the degree of induction to tuberise on single‐node cuttings.     

Screening a cucumber crop during leaf area development reduces yield

In order to reduce heat energy consumption in greenhouse cucumber production, (transparent) screens may be used also during the day, particularly in the early growth phase when high temperatures are required to achieve rapid leaf area development. However, energy savings must be optimised against light reduction‐induced yield loss. For this reason, two experiments were conducted to quantify the effect on photosynthesis and growth of screening cucumber plants during their early growth phase, and on yield in the following generative phase. Screening with different light transmission coefficients was simulated using shading nets. Shading the plants during the first 5 weeks under Central European winter conditions reduced the leaf area by 0.40% per 1% reduction in photosynthetic active radiation (PAR). Moreover, potential leaf net photosynthesis decreased by 0.46% per 1% PAR reduction. A major impact was that the leaf dry matter content, leaf starch content and leaf sugar content of shaded plants diminished significantly. In the course of the following 2 weeks under full light, the leaf photosynthesis of the plants previously shaded recovered fully and the leaf area index rose to 3.3 m² m^?2, considered sufficient for optimal crop photosynthesis. The yield from plants previously shaded diminished slightly as early as from the first harvest week on. These yield losses increased further over the next few weeks, measuring approximately 0.8 kg m^?2 per 1 mol m^?2 day^?1 PAR reduction in the early growth phase. The effect of PAR on plant growth was proportional when relating the PAR integral over the entire experimental period to the total yield and to the total dry matter production, respectively.     

Effects of photoperiod in the glasshouse on the growth of leaves and tillers in three perennial grasses

Leaf and tiller development in vegetative plants of S.₃₇ cocksfoot (Dactylis glomerata L.), S.₂₁₅ meadow fescue (Festuca pratensis Huds.) and S.₂₄ perennial rye-grass (Lolium perenne L.) were measured in photoperiods varied by extending a basic period of natural light with low-intensity artificial illumination so that all plants received approximately the same amount of light each day. Increasing the photoperiod usually increased leaf length and sometimes leaf width, but decreased rate of production of leaves. However, the rate of production of new leaf surface increased with photoperiod. Increasing the photoperiod generally decreased the rate of tillering; thus, plants grown in long days had few tillers with large leaves and sheaths, in short days, plants developed more but smaller tillers.     

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     

Diatom growth responses to photoperiod and light are predictable from diel reductant generation

Light drives phytoplankton productivity, so phytoplankton must exploit variable intensities and durations of light exposure, depending upon season, latitude, and depth. We analyzed the growth, photophysiology and composition of small, Thalassiosira pseudonana, and large, Thalassiosira punctigera, centric diatoms from temperate, coastal marine habitats, responding to a matrix of photoperiods and growth light intensities. T. pseudonana showed fastest growth rates under long photoperiods and low to moderate light intensities, while the larger T. punctigera showed fastest growth rates under short photoperiods and higher light intensities. Photosystem II function and content responded primarily to instantaneous growth light intensities during the photoperiod, while diel carbon fixation and RUBISCO content responded more to photoperiod duration than to instantaneous light intensity. Changing photoperiods caused species‐specific changes in the responses of photochemical yield (e^?/photon) to growth light intensity. These photophysiological variables showed complex responses to photoperiod and to growth light intensity. Growth rate also showed complex responses to photoperiod and growth light intensity. But these complex responses resolved into a close relation between growth rate and the cumulative daily generation of reductant, across the matrix of photoperiods and light intensities.     

Carbon Dioxide and Flowering in Pharbitis nil Choisy

The effects of photoperiod on floral and vegetative development of Pharbitis nil were modified by atmospheric CO₂ concentrations maintained during plant growth. Short day (SD) photoperiods caused rapid flowering in Pharbitis plants growing in 0.03 or 0.1% CO₂, while plants in long day (LD) conditions remained vegetative. At 1 or 5% CO₂, however, flower buds were developed under both the SD and LD photoperiods. Flowering was earliest in the plants exposed to SD at low CO₂ concentrations which formed floral buds at stem node 3 or 4. At high CO₂ concentrations, floral buds did not form until stem node 6 or 7. Both high CO₂ concentrations and LD photoperiods tended to enhance stem elongation and leaf formation.     

Photoperiod and Temperature Interactions in Growth and Flowering of Strawberry

Growth and flowering of strawberry cultivars were studied in controlled environments. Early cultivars adapted to marginal growing areas in Scandinavia initiated flower buds in all photoperiods including continuous light at temperatures of 12 and 18°C. At 24°C they remained vegetative in photoperiods above 14 or 16 h. The later cultivars ‘Senga Sengana’ and ‘Abundance’ did not initiate flower buds in 24-h photoperiods at any of these temperatures. Their critical photoperiod changed from above 16 h at 12°C to about 14 and 13 h at 18 and 24°C, respectively. It is concluded that at high latitudes temperature is as important as photoperiod in controlling flowering in the strawberry. Stolon formation, petiole elongation, and leaf area growth were stimulated by high temperature and long days, usually with optima at 16 h and 18°C for petiole elongation and 16 h and 24°C for stolon formation. Although growth and flowering responses in general were opposite, the results indicate that they are to some extent independent. The photoperiodic growth responses were mainly of morphogenetic nature. Dry weight of stem and leaves was little influenced by photoperiod when the irradiance was kept constant.     

Long day photoperiods and temperature of 20 degrees C induce spermatogenesis in blinded and non-blinded marbled newts during the period of testicular quiescence

Adult male marbled newts (Triturus marmoratus) were collected at the end of the spermatogenesis period and exposed to different photoperiods (natural-daylength-simulated photoperiod, total darkness, 8L:16D, 12L:12D, 16L:8D, and continuous light) for 3 mo. Temperature was maintained at 20 degrees C. Two additional groups of newts were blinded and exposed to either the natural-simulated photoperiod and to 16 h of light per day respectively. Quantitative histologic studies on testicular development and germ cell volume per testis were performed. The newts captured in the field at the beginning (initial controls) or at the end of the experiments (final controls) were in the period of testicular quiescence. Newts kept in total darkness or exposed to a short photoperiod (8L:16D) showed germ cell development up to primary spermatocytes, whereas germ cell development in the newts exposed to long photoperiods (12L:12D or 16L:8D) progressed to elongated spermatids. The newts exposed either to intermediate photoperiods (natural-simulated photoperiod) or to constant light showed an intermediate degree of germ cell development (up to round spermatids). No significant differences between non-blinded and blinded animals were found. These results suggest that (1) mild temperature initiates testicular development in the period of testicular quiescence, (2) long photoperiods associated with mild temperatures produce spermatogenesis in this period, (3) complete darkness or constant light are less effective than some intermediate photoperiod, and (4) the effect of photoperiod on testicular function in newts is not related to ocular photoreception.     

EFFECTS OF PHOTOPERIOD AND KIND OF SUPPLEMENTAL LIGHT ON GROWTH,FLOWERING, AND STEM FASCIATION OF CELOSIA

Piringer , A. A., and H. A. Borthwick . (U.S.D.A., Beltsville, Md.) Effects of photoperiod and kind of supplemental light on growth, flowering and stem fasciation of Celosia. Amer. Jour. Bot. 48(7): 588–592. Illus. 1961.—Four cultivars of Celosia argentea L. var. cristata were grown on photoperiods ranging from 8 hr to continuous light. Supplemental low-intensity incandescent light was used to extend 8 hr of natural light and provide the given photoperiod. In all cultivars, short main stems occurred on photoperiods of 12 or fewer hours and long main stems, due to more nodes, on photoperiods of 16 or more hours. Flowering was a nonobligate short-day response in all cultivars. Plants of certain cultivars tended to have shorter stems and flower later when 8 hr of fluorescent instead of incandescent light was used to provide the 16-hr photoperiod. In 3 of the cultivars studied, photoperiods of 16 or more hours induced marked stem fasciation.     

The Role of Leaves as Inhibitors of Flower Induction in Strawberry: With one Figure in the Text

The effects of various defoliation treatments on flower initiationwere studied in the strawberry var. Talisman, which is a facultativeshort-day plant, with particular reference to differences inthe inductive capacity of leaves of differing maturity. Plants from which all mature leaves had been removed to leaveonly two immature leaves flowered in longer photoperiods thanintact controls, and conversely plants bearing only three fullymature and no immature leaves required a shorter photoperiodfor flower initiation than intact plants. Intact plants in constant darkness and totally defoliated plantsin continuous light both initiated flowers, but intact plantsin continuous light failed to flower. It is submitted that these results provide evidence that thephotoperiodic control of flowering in this plant operates througha flower inhibitor produced in the leaves. They also show that although leaves of any maturity are ableto inhibit flower initiation, under some conditions mature leavesare more inhibitory than immature, and that the inhibitory activityof any leaf decreases with decreasing photoperiod.     

Photoperiodic Effects on the Emanation of Volatiles from Alfalfa (Medicago sativa L.) Florets

Alfalfa (Medicago sativa L.) plants acclimated to photoperiods of 18 hours light, 6 hour dark in plant growth chambers exhibited a daily cyclic pattern of floret volatile emanation with a maximum emanation of about 6.5 nanograms of hydrocarbons/floret·30 minutes. This maximum was reached about 6 to 8 hours into the light period. After 8 hours of light, emanation of volatiles decreased rapidly to less than 0.1 ng/floret·30 min even though light and temperature remained constant. Under continuous illumination, only a small increase of volatile emanation occurred during the following 24 hours. It appeared that a dark period was necessary to promote floret volatile emanation. Floret volatile emanation was drastically affected for at least 7 days following a photoperiod change. A photoperiod change caused 6-fold concentration oscillations every 2 hours. The results are interpreted on the basis of a very active floral metabolism controlled by photoperiodically induced rhythms.