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1.
Avocado plants were kept in growth cabinets at 33°C day, 28°C night (33/28); 25°C day, 20°C night (25/20); and 17°C day, 12°C night (17/12), with a 12-h photoperiod and light intensity of 26000 1x. At 33/28 and 25/20 flowers opened in the afternoon as females and again the following morning as males (type B floral cycle) with some overlap of male and female stages at 25/20. At 17/12 very few flowers had a female stage, the majority opening once only as males. The duration of the flowering period decreased with a rise in temperature as did total number of flowers opening. Reproductive growth was inhibited in favour of vegetative growth at 33/28, as exhibited by smaller floral parts and abscission of buds and flowers. The rate of pollen tube growth increased with a rise in temperature, but abnormal growth was frequently observed at 33/28 and tubes failed to reach the ovary at 17/12. Endosperm and embryo development was observed to occur at 25/20 but not at 33/28 or 17/12 although a positive effect of pollination on fruit retention was evident at 33/28. This effect also occurred at 25/20 but not at 17/12. The most suitable temperature regime for floral behaviour, pollen tube growth and embryo development was 25/20.  相似文献   

2.
The effect of day and night temperatures of 10, 14 and 18°C on growth and flowering under short days was studied with six cultivais of chrysanthemum. A high day temperature resulted in earlier flowering and taller stems, but did not influence flower number and final total fresh weight, and only slightly influenced the distribution of fresh matter over stem, leaves and flowers. A high night temperature resulted in earlier flowering, more flowers and reduced stem and leaf weight. It did not affect leaf number and it influenced height and total fresh weight only slightly. Except for height, the day temperature acted independently from the night temperature. The cultivars responded similarly, except for two cultivars which generally did not flower at 10/10,10/14 and 14/10°C D/N. One cul-tivar produced more flowers at 14 than at 18°C.  相似文献   

3.
Night temperatures warmer than those normally used in commercial production systems promoted vegetative growth in Tagetes patula and Matthiola incana seedlings. In the short (8 h) daylength regime employed, and with a day temperature of 16°C, cool nights (8°C) had a detrimental effect, especially when imposed for 6 weeks from pricking-out rather than later. Night temperatures between 8°C and 16°C did not substitute for the long-day requirement for flowering in Matthiola after 11 weeks' growth, and there was no advantage with respect to vegetative growth in maintaining night temperatures above 12°C. Warmer nights from pricking-out promoted flowering in Tagetes but if applied later (during weeks 7–11) the positive effects were largely on vegetative growth. The implications of these findings for commercial horticulture are discussed.  相似文献   

4.
《Scientia Horticulturae》2001,87(4):303-309
Rice flower (Ozothamnus diosmifolius, Vent.), native to east Australia, is a spring flowering perennial shrub. It is a new cut flower plant, recently introduced into cultivation in Australia and in Israel. Its response to environmental conditions, which affect growth and flowering, are not yet known. The purpose of the present study was to evaluate the effects of growth temperature, photoperiod and total solar energy on flowering. Experiments were conducted with plants of the cv. Cook’s Snow White. Plants were grown in three cycles under controlled conditions in the phytotron, at four day/night temperature regimes: 17/9, 20/12, 23/15 and 26/18°C. Two photoperiods — short day (SD) of 10 h natural day light and long day (LD) of 10 h natural light plus 10 h incandescent light — were employed. High temperatures enhanced vegetative growth but blocked flowering under both LD and SD. Under medium–moderate temperatures plants were absolute LD plants and did not flower under SD conditions. Under lower temperatures plants flowered under both LD and SD, but SD delayed flowering. High total solar radiation under LD did not affect flowering time but greatly promoted the number of flowering stems.  相似文献   

5.
Summary

The impact of day and night temperatures on pot chrysanthemum (cultivars ‘Covington’ and ‘Irvine’) was assessed by exposing cuttings, stuck in weeks 39, 44, and 49, to different temperature regimes in short-days. Glasshouse heating set-points of 12°, 15°, 18°, and 21°C, were used during the day, with venting at 2°C above these set-points. Night temperatures were then automatically manipulated to ensure that all of the treatments achieved similar mean diurnal temperatures. Plants were grown according to commercial practice and the experiment was repeated over 2 years. Increasing the day temperature from approx. 19°C to 21°C, and compensating by reducing the night temperature, did not have a significant impact on flowering time, although plant height was increased. This suggests that a temperature integration strategy which involves higher vent temperatures, and exploiting solar gain to give higher than normal day temperatures, should have minimal impact on crop scheduling. However, lowering the day-time temperature to approx. 16°C, and compensating with a warmer night, delayed flowering by up to 2 weeks. Therefore, a strategy whereby, in Winter, more heat is added at night under a thermally-efficient blackout screen may result in flowering delays. Transfers between the temperature regimes showed that the flowering delays were proportional to the amount of time spent in a low day-time temperature regime. Plants flowered at the same time, irrespective of whether they were transferred on a 1-, 2-, or 4-week cycle.  相似文献   

6.
Summary

Floral induction in tropical trees generally follows a check in vegetative growth. However, it is not easy to identify the environmental factors involved in flowering, which normally occurs during the dry season when temperatures are also often lower. The separate and combined effects of temperature and water supply on floral induction were investigated in ‘Hass’ avocado (Persea americana), ‘Lisbon’ lemon (Citrus limon). ‘Wai Chee’ litchi (Litchi chinensis) and ‘Sensation’ mango (Mangifera indica). Low temperatures (15°/10°C or 15°/10°C and 20°/15°C compared with 30°/25°C and 25°/20°C) generally decreased vegetative growth and induced flowering in well-watered avocado, litchi and mango. A pre-dawn leaf water potential (ψL) of ?1.7 to ?3.5 MPa compared with ?0.4 to ?0.7 MPa in control avocado and litchi, and a pre-dawn relative water content (R.W.C.) of 90-93% compared with 97% or above in control mango plants also reduced or eliminated vegetative growth, but did not induce flowering. Low temperatures (15°/10°C compared with 20°/5°C, 25°/20°C or 30°/25°C) and water stress (pre-dawn ψL of ?2.0 to ?3.5 MPa compared with ?0.7 to ?0.8 MPa in controls) reduced or eliminated vegetative growth in lemon. In contrast to the response in avocado, litchi and mango, flowering in lemon was very weak in the absence of water stress at 15°/10°C or outdoors in Brisbane in subtropical Australia (Lat. 28°S), and was greatest after a period of water stress. The number of flowers increased with the severity and duration of water stress (two, four or eight weeks) and was generally greater after constant rather than with cyclic water stress. In lemon and litchi, net photosynthesis declined with increasing water stress reaching zero with a midday ψL of ?3.5 to ?4.0 MPa. This decline in carbon assimilation appeared to be almost entirely due to stomatal closure. Despite the reduction in midday CO2 assimilation, starch concentration increased during water stress, especially in the branches, trunk and roots of lemon. Leaf starch was uniformly low. The number of flowers per tree in lemon was strongly correlated with starch in the branches (r2=77%, P<0.01) and roots (r2=74%, P<0.001). In litchi, starch was lower than in lemon roots and was not related to flowering.

In separate experiments to test the interaction between temperature and water supply, low day/night temperatures (23°/18° and 18°/15°C compared with 29°/25°C) reduced vegetative growth and induced flowering in avocado, litchi and mango. None of these species flowered at 29°/25°C or as a result of water stress (ψL of ?1.5 MPa compared with ?0.3 MPa for avocado and ?2.0 MPa compared with ?0.5 MPa for litchi, and R.W.C, of 90-93% compared with 95-96% in mango). In contrast, in lemon, flowering was very weak (<10 flowers per tree) in the absence of water stress (pre-dawn ψL of ?2.0 MPa compared with ?0.5 MPa) and was only heavy (>35 flowers per tree) after stressed trees were rewatered. There were slightly more flowers at 18°/15°C than at 23°/18° and 29°/25°C in control plants, but no effect of temperature in stressed plants. Starch concentration in the roots of avocado, lemon, litchi and mango was generally higher at 18°/15°C and 23°/18°C than at 29°/25°C. Water stress increased the starch concentration in the roots of lemon and litchi and decreased it in avocado. There was no effect in mango. There was a weak relation (r2=57%, P<0.05) between the number of flowers per tree in lemon and the concentration of starch in the roots. In contrast, there was no significant relationship between flowering and starch levels under the various temperature and water regimes in the other species. In another experiment, only vegetative growth in litchi and mango occurred at 30°/25°C and only flowering at 15°/10°C. Six weeks of water stress (pre-dawn ψL of ?2.5 MPa compared with ?1.0 MPa or higher in litchi, and R.W.C, of 90-93% compared with 95% or higher in mango) in a heated glasshouse (30°C days/20°C night minimum) before these temperature treatments did not induce flowering.

Temperatures below 25°C for avocado and below 20°C for litchi and mango are essential for flowering and cannot be replaced by water stress. The control of flowering in lemon over the range of day temperatures from 18°C to 30°C differed from that of the other species in being mainly determined by water stress. Flowering was generally weak in well-watered plants even with days at 18°C. Starch did not appear to control flowering.  相似文献   

7.
The relationship between flowering and day and night temperatures in cacao has been studied over a period of nine months in controlled environment rooms, with clonal trees which were 13 months old at the start of the experiment.

All the plants started to flower at the same time, but thereafter there was a marked response to temperature. Flowering was greater at day temperatures of 80° and 86° F. (26 .7°, 30° C.) than at day temperatures of 74° F. (23–3° C.) and, at each level of day temperature, flowering was greater at a night temperature of 80° F. than at one of 74° or 86° F. The relative effects of temperature were similar on numbers of flowering cushions per plant and of flowers per cushion.

There was no apparent relationship bfetween the amount of flowering and new leaves (flushes) produced, either at the time of flowering or at any period before. Neither was there a quantitative relationship between flowering and leaf area of the plants, though, in general, the treatments that resulted in the greatest leaf areas also resulted in the greatest numbers of flowers. A possible relationship was suggested between the number of flowering cushions and the total extension growth of the branches.  相似文献   

8.
Starting at full bloom, 4 temperature treatments were applied to 3-year-old ‘Golden Delicious’ and ‘Cox's Orange Pippin’ trees. Either 17 or 24° C were applied in 3 successive periods of 5–6 weeks each.In ‘Golden Delicious’, exposure to 24° C during the first 5 weeks after full bloom enhanced shoot growth and reduced flower-bud formation in spur buds. The difference in temperature-regime during the third period did not affect either growth or flowering. Almost all apical shoot buds became floral, irrespective of treatment.‘Cox's Orange Pippin’ trees maintained at 24° C throughout grew more vigorously than did those kept at 17° C continuously, but flowering-abundancy was the same. Lowering of the temperature in the last period before harvest did not influence shoot growth, but markedly reduced flowering of both spur buds and apical shoot buds.In a second experiment, a night temperature of either 20 or 10° C was applied in 2 successive periods to 3-year-old ‘Cox's Orange Pippin’ trees kept at a day temperature of 20° C throughout. Lowering of the night temperature in the middle of the season reduced flower-bud production, but there was no difference in growth vigour compared with 20° C continuously.It is postulated that temperature affects flowering in two opposite ways, whose relative importance determines the net result.  相似文献   

9.
Chrysanthemum plants were exposed to 16°C day-temperature, 11°C night-temperature, 13°C soil-temperature, to be indicated as 16/11/13°C, or to 16/11/25°C, 20/16/18°C, or 20/16/25°C, first long day, then short day, (long day = 12-h light period with 3-h night break; short day = 12-h light period) from planting to harvest in controlled environments to study the effects of soil heating on growth and flowering. There were significant, but not substantial, effects of soil heating on leaf area, percent soluble carbohydrate, flower bud diameter, days to visible bud and some other parameters. Two winter cultivars responded similarly, while 2 summer cultivars differed in flowering-response to soil heating. An experiment was also conducted using 16/11/25°C day/night/soil temperatures during long days, short days or throughout the complete growth cycle, with 16/11/13°C day/night/soil temperatures at other times. Soil heating during long days resulted in the highest quality flowers. Soil heating during short days or throughout the growth period resulted in most rapid flowering but decreased flower quality.  相似文献   

10.
Long day promotes flowering of Gysophila paniculata L cultivar ‘Bristol Fairy’. Repeated treatments with GA3 or GA4 + 7 in short days did not promote flowering. The long photoperiod is effective only at relatively high temperatures. At night temperatures below 12°C, the plants remain vegetative even in long days. Efficient artificial lighting is from incandescent lamps at 60–100 lux. Fluorescent lighting (Cool-White) is not effective. Lighting of 4 hours as a night-break or at the end of the night were equally effective, but 4 hours lighting as a day-extension was less effective. Whole-night lighting promoted flowering more than any of the 4-hour lighting regimes. Cyclic lighting of one third light in each cycle promoted flowering to the same extent as continuous lighting. Light intensity during the day has a decisive effect on flower production.  相似文献   

11.
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12.
Summary

Moderate day/night temperatures (20/15° v. 15/10°C) increased vegetative growth and reduced flowering in the seven litchi cvs Tai So, Bengal, Souey Tung, Kwai May Pink, Kwai May Red, Salathiel and Wai Chee. At higher temperatures (25/20° and 30/25°C), vegetative growth was promoted further and flowering eliminated. Temperature also influenced the type of inflorescence formed. More leaves were formed on the panicles of trees growing at 20/15° than at 15/10°C. All terminal shoots on all cultivars produced panicles at 15/10°C. The relative order for the amount of flowering at 20/15°C was: ‘Wai Chee’>‘Salathiel’>‘Kwai May Pink’>‘Tai So’>‘Bengal’>‘Souey Tung’>‘Kwai May Red’. Cultivars which were vigorous at high temperatures produced fewer panicles at 20/15°C and fewer leafless panicles at 15/10°C. Only small differences were observed in the leaf water potential and the nutrient status of the shoots at different temperatures. Vigour and flowering of the cultivars in the glasshouse generally reflected field performance in subtropical Australia (Lat. 27°S). Low vigour could be useful for selecting litchi cultivars for good fruiting in environments with warm autumns and winters.  相似文献   

13.
《Scientia Horticulturae》2005,105(1):127-138
Experiments were performed with the Chilean geophyte Zephyra elegans, a potential cut flower, to evaluate the effect of corm weight and storage temperature on corm dormancy, and to determine the effect of day and night growing temperatures on its growth and flowering. Z. elegans has a deciduous and synanthous growth habit and the corm is replaced annually. Dormant corms were stored at different constant temperatures or temperature combinations from 20 to 40 °C. Corms released from their dormancy were grown at 15/10, 20/15, or 25/20 °C day/night temperatures. Corms of various weights were planted at the same date after being stored dry at 25 °C for 22 weeks. They all emerged 19–38 days after planting, showing that dormancy release was not affected by corm weight. A 20-week corm storage treatment at a constant 25 °C resulted in the most rapid corm sprouting. Sprouting percentage was reduced at higher or lower storage temperatures. Temperature also affected plant growth. When plants were grown at 15/10 or 20/15 °C they emerged and flowered more rapidly than when they were grown at 25/20 °C. The latter growing temperature also resulted in poor flower quality.  相似文献   

14.
Summary

‘Korona’, ‘Elsanta’, ‘Bounty’ and ‘Senga Sengana’ strawberry (Fragaria × ananassa Duch.) plants, were placed at constant temperatures of 9, 15 or 21°C and daylengths of 8 h (short day) or 24 h (long day). The plants were given different numbers of short-day (SD) cycles, and flowering and growth were studied. ‘Korona’ and ‘Elsanta’ were responsive to both short-day treatment and temperature, with optimum flowering at 15°C and 24 SD. ‘Bounty’ was more responsive to temperature, inducing flowers independently of the number of SD cycles at 9°C and 15°C. In ‘Senga Sengana’ flowering was induced independently of temperature and the number of SD cycles, indicating that it had a stronger dependence on other environmental effects. The effect of the number of short-day cycles and the temperature on vegetative growth variâtes such as the number of stolons and daughter plants, the length of flower trusses and petiole length were also studied.  相似文献   

15.
N. flexuosa alba is a perennial bulbous member of the Amaryllidaceae and an attractive new ornamental. In the bulb, inflorescence buds are formed periodically under any circumstances which allow growth. The problem was that quite often these buds do not elongate, and desiccate prematurely, so that poor flowering results.Light was found not to be a factor in flowering, neither energetically nor photo-periodically, but temperature turned out to be limiting. Good flowering occurred after growth at temperatures of 9 or 13°C, 17 and 21°C being too high. The combination of 9°C during growth and 21°C during storage resulted in 100% satisfactory flowering and an acceptable bulb growth. Gibberellic acid did not effect flowering.  相似文献   

16.
With the aim of obtaining information about light and temperature relationships during the early weeks of growth of young tomato plants, measurements of the weekly dry weight increments were made with plants up to six weeks old. Growth took place in natural light conditions during a number of winter periods (October to March). The daily light-time integrals (foot candle hours) were recorded throughout the investigation. In three experiments, each extending over a whole winter period, plants were grown at one-day temperature, but at three levels of night temperature, namely (a) 4° F. lower than the day, (6) equal with the day, and (c) 4° F. higher than the day. The day temperature was 6o° F. (15 ? 5° C.), 64° F. (68°C.) and 68°F. (20°C.) respectively for the three experiments. The results are summarized as follows :

1. With each day temperature, growth rates were lowest when night temperature was lower than the day.

2. Comparison of the effects of the constant temperature regimes with the high night temperature regimes showed that with the day temperature at 60° F. the growth rate was generally higher when the night temperature was high. With higher day temperatures, however, this was not the case.

3. There was little evidence that over this temperature range the temperature inducing maximum growth was related either to the light conditions or to the age of the plant.

4. The response to night temperature was small by comparison with response to that of the day.

5. The results suggest that in winter highest growth rates will be achieved if the night temperature is not lower than 64° F. and the day not lower than 68° F.

The results of an experiment designed to evaluate the separate effects of day and night temperatures showed that, over the temperature range 6o° F. to 68° F., dry weight increased with the night temperature. However, a much larger increase resulted with a comparable temperature rise during the day. Stem length was unaffected by the level of the night temperature but increased markedly with the day temperature.

The periods from pricking-out to both initiation and anthesis of the first two inflorescences were recorded for plants growing at 6o° F., 64° F. and 68° F. The temperature effect on the period to initiation was small. The inverse relationship between temperature and the period to anthesis was especially marked in low light conditions.

The value of adjusting both the day and night temperatures in accordance with the day-to-day fluctuations of the natural light was assessed by comparison with other temperature regimes having the same mean over each 24 hours. In general, flowering and fruiting was earliest when the day and night temperatures were equal. No evidence was found to justify the technique of adjusting the temperature in accordance with the natural light.  相似文献   

17.
Under controlled conditions, 3-year old ‘Golden Delicious’ and ‘Cox's Orange Pippin’ trees were exposed to 2 temperatures (high: 24° and low: 17° or 19° C) in various treatments in a 4-month period starting at full bloom. In general, shoot growth was reduced at the low temperature. For ‘Golden Delicious’ flowering did not respond to the various treatments; in ‘Cox's Orange Pippin’ it was stimulated at the low temperature.A rise in temperature from 17° to 24° C seven weeks before harvest, given to ‘Cox's Orange Pippin’ trees kept at 17° C from full bloom, reduced flower-bud formation and stimulated growth. A similar temperature increase applied to trees maintained at 24° C for 4–5 weeks after full bloom favoured flower-bud formation, but did not affect growth.The inhibitory effect of the high temperature on flowering is discussed in terms of an increase of the plastochron under the influence of gibberellins produced by the growing shoot tips.  相似文献   

18.
Summary

This study addresses the effects of air temperature and plant growth regulators on anthocyanin synthesis, sugar content and phenylalanine ammonia-lyase (PAL) activity in chicory (Cichorium intybus L.). Anthocyanin in chicory was synthesised at the highest level under 15°/10°C (day/night) temperatures, followed by 20°/15°C, and 25°/20°C; while synthesis was inhibited > 90% at 30°/25°C, resulting in an almost green colour. Sugar contents paralleled anthocyanin development under the same temperatures. The plant growth regulators, abscisic acid (ABA), ethephon and uniconazole all stimulated anthocyanin synthesis, with uniconazole treatment showing the greatest effect. Gibberellic acid (GA3) inhibited anthocyanin development, while GA3 in combination with uniconazole alleviated this inhibition.

PAL activity was higher at 15°/10°C or 20°/15°C (day/night) temperatures when plants were treated with ABA, ethephon or GA3, than at 25°/20°C and 30°/25°C (day/night) temperatures. These results suggest that, under lower temperatures, plant growth regulators may play an important role in anthocyanin synthesis and PAL activity in chicory.  相似文献   

19.
The effect of a wide range of soil temperatures (6–26°C) on growth and flowering of Chrysanthemum morifolium Ram. ‘Horim’ were studied at the favourable air temperature of 18°C. Shoot growth was severely reduced at soil temperatures below 10°C which may be explained by poor root growth, while flowering was enhanced by approximately 2 days compared to higher soil temperatures. Increasing the soil temperature to 18°C was beneficial. Further increase had no positive effect on growth. Measurements of net photosynthetic rates revealed no effect of lowering soil temperatures from 18 to 6°C.Mother plants grown at 18°C air temperature revealed no effect of soil temperatures ranging from 13 to 21°C on number and fresh weight of the cuttings. Neither did mother plants grown at the less favourable air temperatures of 12 or 15°C. Cutting production was, however, affected by air temperature.  相似文献   

20.
Summary

Photoperiod and temperature control of flowering in a number of perpetual-flowering or everbearing strawberry cultivars of widely varying pedigree has been studied in controlled environments. Flower bud initiation in the cultivars ‘Flamenco’, ‘Ridder’, ‘Rita’ and ‘Rondo’ was significantly advanced by long-day (LD) conditions at temperatures of 15°C and 21ºC; while, at 27ºC, flowering took place under LD conditions only. Some plants of the seed-propagated F1-hybrid ‘Elan’, raised at 21°C, also flowered under short-day (SD) conditions at 27°C, but reverted to the vegetative state after a few weeks when maintained under these conditions. When vegetative plants growing in SD at 27°C were transferred to LD conditions at the same temperature, they consistently initiated flower buds and started flowering after about 4 weeks. At such a high temperature, flowering could thus be turned on and off by switching between SD and LD conditions. This applied to all the cultivars studied. Also the cultivar ‘Everest’, which was tested only at 21°C, produced similar results. Night interruption for 2 h was effective in bringing about the LD response. At 9°C, flowering was substantially delayed, especially in ‘Flamenco’ and, at this temperature, flowering was unaffected by photoperiod. Runner formation was generally promoted by high temperature and SD conditions, but the photoperiodic effect varied between experiments. We conclude that everbearing strawberry cultivars, in general, whether of the older European-type or the modern Californian-type originating from crosses with selections of Fragaria virginiana ssp. glauca, are qualitative (obligatory) LD plants at high temperature (27°C), and quantitative LD plants at intermediate temperatures. Only at temperatures below 10°C are these cultivars day-neutral.  相似文献   

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