Semidian rhythmicity in the flowering response of Pharbitis nil to changes in temperature

1998 ◽  
Vol 25 (2) ◽  
pp. 183 ◽  
Author(s):  
O.M. Heide ◽  
R.W. King ◽  
L.T Evans

Our earlier experiments on flowering in the short day plant Pharbitis nil involved far- red/dark (FR/D) interruptions of 90 min duration at various times during a continuous light, constant temperature period before a single inductive dark period. They revealed a rhythm with a period of 12 h, hence semidian. We concluded that the phasing of this semidian rhythm determined the length of darkness required for floral induction. This conclusion has since been challenged so we sought other pretreatments which reveal the semidian rhythm. Interruptions at 12°C–17°C for 45–90 min at various times prior to the inductive dark period were as effective as FR/D in eliciting the semidian rhythm, with significant effects on flowering persisting for at least three cycles in constant conditions in continuous light. The rhythmic response to 12°C pretreatments was 3 h out of phase with that to FR/D pretreatments. Flowering responses to the semidian rhythm exposed by 12°C pretreatments were additive to and independent of those to a circadian rhythm. Some evidence was obtained of reversal of the inhibition or promotion of flowering by FR/D or 12°C by exposure immediately afterwards to the other pretreatment at times of their opposite effect. Pretreatments at 12°C, like those with FR/D, either reduced (if promotive) or extended (if inhibitory) the length of the dark period required for floral induction in this short day plant.

10.5586/1201 ◽  
2014 ◽  
Vol 60 (1-2) ◽  
pp. 133-138
Author(s):  
Joanna Czaplewska ◽  
Jan Kopcewicz

The short-day plant, <i>Pharbitis nil</i>, requires only a single inductive cycle with a 16-hour dark period for flowering. The mitotic activity in the shoot apices was studied directly after the termination of the inductive photoperiod. A pronounced rise in the mitotic index was found in the 2nd and the 8th-14th hours. Control plants grown under noninductive conditions (continuous light, a light interruption in the middle of the dark period) did not flower and did not show an increased mitotic index. The increased mitotic activity in the shoot apices of <i>Pharbitis</i> seems to be causally connected with the phytochrome-controlled entry of the plants into the state of generative induction.


HortScience ◽  
1990 ◽  
Vol 25 (9) ◽  
pp. 1077f-1077
Author(s):  
Jason Tutty ◽  
Peter Hicklenton

The rate of internodal extension of chrysanthemum (Dendranthema grandiflora Tzvelev. cv. Envy) under various temperature and photoperiod conditions was studied to determine whether reproducible diurnal patterns of growth existed and whether any such patterns conformed to an endogenous circadian rhythm. Stem growth was monitored continuously by means of linear displacement voltage transducers. At constant temperature and under 11 h light/13 h dark photoperiod, stem elongation followed a clearly defined pattern consisting of a peak in rate immediately after the dark to light transition and then a gradual decline until the start of the dark period. During darkness, elongation rate increased and reached a maximum approximately 8 hours after the light to dark transition. This pattern differed when light period temperature was either above or below dark period temperature, but these patterns were also highly reproducible. When plants were subjected to continuous light at constant temperature, the rhythm of stem elongation initially showed a periodicity of approximately 27 hours. After 2 or 3 diurnal cycles the rhythm was less distinct and the rate became essentially constant. Furthermore, the interruption of a long period of continuous light with a 13 h dark period did not restore the rhythm. These findings do not support the existence of an endogenous circadian rhythm of stem elongation. Diurnally-cued rhythms do, however, exist and can be modified by temperature.


HortScience ◽  
1990 ◽  
Vol 25 (9) ◽  
pp. 1077F-1077
Author(s):  
Jason Tutty ◽  
Peter Hicklenton

The rate of internodal extension of chrysanthemum (Dendranthema grandiflora Tzvelev. cv. Envy) under various temperature and photoperiod conditions was studied to determine whether reproducible diurnal patterns of growth existed and whether any such patterns conformed to an endogenous circadian rhythm. Stem growth was monitored continuously by means of linear displacement voltage transducers. At constant temperature and under 11 h light/13 h dark photoperiod, stem elongation followed a clearly defined pattern consisting of a peak in rate immediately after the dark to light transition and then a gradual decline until the start of the dark period. During darkness, elongation rate increased and reached a maximum approximately 8 hours after the light to dark transition. This pattern differed when light period temperature was either above or below dark period temperature, but these patterns were also highly reproducible. When plants were subjected to continuous light at constant temperature, the rhythm of stem elongation initially showed a periodicity of approximately 27 hours. After 2 or 3 diurnal cycles the rhythm was less distinct and the rate became essentially constant. Furthermore, the interruption of a long period of continuous light with a 13 h dark period did not restore the rhythm. These findings do not support the existence of an endogenous circadian rhythm of stem elongation. Diurnally-cued rhythms do, however, exist and can be modified by temperature.


2006 ◽  
Vol 84 (12) ◽  
pp. 1908-1916
Author(s):  
Natsuko I. Kobayashi ◽  
Keitaro Tanoi ◽  
Tomoko M. Nakanishi

We present the potential involvement of Mg2+ in the flowering mechanism in the shoot apex of the short-day plant Pharbitis nil (L.). To analyze elemental distribution in shoot apical meristems, fluorescence staining methods with Mag-fluo-4 AM and Fluo-3 AM were used. The former is sensitive to both Mg2+ and Ca2+, and the latter is a specific Ca2+ indicator. When plants were grown under continuous light conditions, some cells with intensive fluorescence of Mg2+ appeared in the top layers of the shoot apical meristem. During growth in the vegetative phase, cells in the center of the top layers accumulated large amounts of Mg2+. Exposure to a single 16 h short-day treatment induced the flowering process and dramatically reduced the fluorescence associated with Mg2+ accumulation in the top layers, suggesting that Mg2+ contributes to the flower induction process. The fluorescence associated with Ca2+ did not show this distribution difference between growth phases. A night-break treatment also influenced the fluorescence pattern. It was suggested for the first time that Mg2+ plays an important role in flower induction.


2003 ◽  
Vol 58 (3-4) ◽  
pp. 220-224 ◽  
Author(s):  
Masayuki Suzuki ◽  
Masaya Mizoguchi ◽  
Fumihiko Yano ◽  
Utako Hara ◽  
Mineyuki Yokoyama ◽  
...  

We investigated the effects of catecholamine on flower-induction in P. nil (cv. Violet). GCSIM analysis identified dopamine for the first time in P. nil seedlings. Dopamine levels in the cotyledons did not show a significant change during the inducing dark treatment. The dopamine content of cotyledons exposed to various durations of darkness were 0.1-0.2 nmol/ g fresh weight. The same content was found when cotyledons were exposed to continuous light.


1962 ◽  
Vol 53 (2) ◽  
pp. 417-436 ◽  
Author(s):  
W. A. L. David ◽  
B. O. C. Gardiner

The work described in this paper forms the final part of an investigation into the biology and breeding of Pieris brassicae (L.) in captivity and concerns the larvae and the pupae.The larvae of the Cambridge stock used in this investigation were found to pass through five instars in the course of their development at temperatures between 12·5 and 30°C. At the lower temperature, development was completed in 46·5 days and at the higher temperature in 11 days.The average width of the head capsules in each instar was not affected by the temperature at which the larvae were reared, it showed little variation, and it never overlapped with that of the preceding or ensuing instar and, therefore, provides a certain way of determining the instar of any larva.At 20°C., isolated larvae and larvae kept in crowded cultures completed their development in approximately the same time—19·6 and 18·8 days, respectively.The average consumption of food during the whole larval period was determined in two experiments, in which it was found to be 1·42 and 1·29 g. of fresh leaves per g. of larva per day, respectively.The duration of the pupal period ranged from 7·5 days at 30°C. to about 40 days at 12·5°C.The adults showed a definite diel rhythm of emergence. When kept at a constant temperature, with a photoperiod from 6 a.m. to 10 p.m., nearly all the insects emerged during the dark period and that immediately following it—actually between the hours of 1 a.m. and 9 a.m. If the photoperiod is displaced 12 hours, the emergence is also displaced by the same amount, to correspond with the new dark period. If, instead of keeping the temperature constant, with the photoperiod 6 a.m. to 10 p.m., it is allowed to fluctuate, as it does naturally in June, the emergence is delayed and instead of occurring in darkness and the early hours of the morning as it does at a constant temperature, it takes place mainly during the morning and the afternoon. When insects, which have been reared at a constant temperature and a photoperiod from 6 a.m. to 10 p.m., are allowed to emerge at a constant temperature, in continuous light, there is very little evidence of a diel rhythm of eclosion but if the insects are kept in continuous darkness they show a definite rhythm of emergence. If the pupae are kept in constant light but the temperature is allowed to fluctuate, most of the adults emerge during the warmer period of the cycle.Diapause in the pupa of P. brassicae is mainly determined by the photoperiod and the temperature during the larval stages. At 20°C., larvae reared in continuous darkness do not form diapause pupae; as the daily photoperiod increases, the percentage of diapause pupae formed also increases until, at a photoperiod of 12 hours, only diapause pupae are formed. Beyond this point the percentage of diapause pupae again declines until, with a photoperiod of about 18 hours, only non-diapause pupae are formed. At higher temperatures similar trends are observed but lower percentages of diapause pupae are formed at all photoperiods.In P. brassicae there is no evidence that a short, sharply defined period of a day or two exists in the course of the life of the larvae during which the photoperiod operates to influence diapause.Non-diapause pupae produced from larvae reared in continuous darkness and from larvae reared in long days (over 15 hours' light) appear to contain a growth-promoting hormone capable of causing the emergence of diapause pupae.


2014 ◽  
Vol 64 (1) ◽  
pp. 45-50 ◽  
Author(s):  
Halina Kulikowska-Gulewska ◽  
Mariusz Cymerski ◽  
Joanna Czaplewska ◽  
Jan Kopcewicz

The endogenous content of IAA in the cotyledons of <i>Pharbitis nil</i> is low before and during the first half of the inductive 16-h-long dark period. From the 8th to the 12th hour the level of IAA increased and then again was going down at the end of a dark period. Exogenous IAA applied to the cotyledones before and during the first half of the inductive dark period inhibits flower bud formation. The application of IAA to shoot apex also resulted in the inhibition of flowering. Experiments with TIBA, an auxin polar transport inhibitor, and PCIB, an auxin action inhibitor, have shown that auxin polar transport in cotyledones and long-distance auxin transport from cotyledones to shoot apex play an important role in IAA inhibition of flower bud formation. It suggests that auxins play their role not only at the level of floral induction in cotyledones, but also in the later events of floral evocation and differentiation in shoot apex.


1974 ◽  
Vol 1 (3) ◽  
pp. 445 ◽  
Author(s):  
RW King

Seedlings of Phavbitis nil and Chenopodium rubrum flower in response to a single inductive dark period preceded and followed by continuous fluorescent light. However, when a far-red irradiation for 1 h or longer was substituted for fluorescent light, the flowering response to an ensuing dark period could be completely inhibited or enhanced up to threefold depending on when the far-red exposure commenced. Evidence of red/far-red photoreversibility established phytochrome as the photoreceptor controlling these responses. There was no indication of the involvement of photosynthetic pigments. For P. nil prolonged exposure (1.5-6 h) to far-red radiation during the photoperiod could shorten (2-3 h) or lengthen (2 h) the duration of darkness required for flowering. The degree of change depended on whether the far-red radiation was imposed just prior to darkness (shortening) or about 9 h prior to darkness (lengthening). In a similar manner the spectral composition of the photoperiod influenced the timing during darkness for earliest sensitivity to brief (5 min) red light interruptions. The shorter the critical dark period, the earlier in darkness the seedlings became sensitive to red light interruptions of darkness. It is clear that the form of phytochrome during the photoperiod influences the timing of phytochrome- linked processes in darkness. Two explanations discussed are a coupling via rhythmic changes in substrate on which phytochrome acts, and an effect on phytochrome reactions which alters the timing of Pf, disappearance during a subsequent dark period.


2007 ◽  
Vol 19 (10) ◽  
pp. 2988-3000 ◽  
Author(s):  
Ryosuke Hayama ◽  
Bhavna Agashe ◽  
Elisabeth Luley ◽  
Rod King ◽  
George Coupland

Sign in / Sign up

Export Citation Format

Share Document