scholarly journals The effect of inductive photoperiod on flower formation and phytohormones level in a long day plant Hyoscyamus niger L.

2015 ◽  
Vol 48 (2) ◽  
pp. 255-265 ◽  
Author(s):  
J. Kopcewicz ◽  
G. Centkowska ◽  
K. Kriesel ◽  
Y. Yatorska

The anatomical and hormonal investigations on a long day plant <i>Hyoscyamus niger</i> L. during the time of the generative photoinduction have been conducted. The plants were grown during 75 days on a short photoperiod and then they were transferred to long day conditions. The earliest anatomical symptoms of flower initiation were noticed after four long photoperiods. The inductive photoperiod causes also a general increase in the amounts of phytohormones. During the flower evocation the intensive accumulation of cytokinins and gibberellins in leaves takes place. The post-inductive period, in which the development of flower elements happens, is characterized by changing amount of phytohormones. The content of hormonal substances is subjected to the rhytmical changes related to the periods of light and darknees in the twenty four hours' cycle.

2014 ◽  
Vol 51 (1) ◽  
pp. 51-58
Author(s):  
Jan Kopcewicz ◽  
Gabriela Centkowska

Night-breaks caused both stimulated shoot growth and caused formation of flowers as well as a general increase in the content of phytohormones in leaves of the long-day plant <em>Hyoscyamus niger</em> L. At the time of flower formation in night-break treated plants, new gibberellin-like substances also appear. The results show that night-breaks cause similar changes in the phytohormones content as a long inductive photoperiod. It may be assumed that independently of the way of induction, the generative differentiation of long-day plants is always accompanied by a general increase in the amount of endogenous hormones and the appearance of new gibberellins. These results suggest the possibility of a morphogenetic role of hormones, especially gibberellins, in the phenomena of flower formation and differentiation.


2014 ◽  
Vol 49 (3) ◽  
pp. 245-258
Author(s):  
Jan Kopcewicz ◽  
Gabriela Centkowska ◽  
Krystyna Kriesel

The investigations concern changes in the content of endogenous phytohormones in the leaves of the long-day plant <em>Hyoscyamus niger</em> L. during variable photoperiods applied before and after flower initiation. The results show that alternation of inductive photoperiods with short days leads to quantitative changes in the content of phytohormones. The changeable photoperiod leads to a general decrease in the contents of gibberellins, cytokinins and auxins during the short noninductive days both before and after flower initiation. Alternation of the inductive photoperiod with short days does not influence the content of abscisic acid-like substances before flower initiation and causes an increase of the amount of inhibitors in the postinductive period. The content of hormonal substances is subjected to rhytmical changes related to the periods of light and darkness in the twenty-four hours' cycle.


2014 ◽  
Vol 52 (1) ◽  
pp. 71-75
Author(s):  
Jan Kopcewicz ◽  
Gabriela Centkowska

Gibberellins (GA<sub>4+7</sub>) and gibberellin-like substances isolated from generatively induced black henbane (<em>Hyoscyamus niger</> L.) bring about the growth of shoots and a partial differentiation of axillary meristem in black henbane plants grown under non-inductive light conditions. Long-lasting application of gibberellins, however, did not result in full development of flowers in the majority of the plants investigated. Thus, it seems, that gibberellins are not specific flowering hormones in black henbane - a long-day plant.


HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 509a-509
Author(s):  
C.E. Wieland ◽  
J.E. Barrett ◽  
D.G. Clark ◽  
G. J. Wilfret

Four poinsettia cultivars were grown in glass greenhouses in Gainesville, Fla., in the Fall 1997 to evaluate differences in floral initiation and subsequent development. Three means of regulating photoperiod were 1) natural days 2) long-day lighting to 6 Oct. and then natural days (lights out) 3) long-day lighting to 6 Oct., and then short-day conditions by black cloth for 15 h (black cloth). At 2-day intervals, sample meristems were collected and examined for initiation of reproductive development. Average minimum and maximum temperatures during the first two weeks of October were 22 and 29 °C, respectively, with an average temperature of 25.3 °C. The overall average temperature was 23.2 °C from planting to anthesis. Differences in anthesis dates among cultivars were primarily due to time to initiation vs. rate of development. Under natural days, `Lilo' initiated first on 8 Oct. and `Freedom', `Peterstar', and `Success', followed by 6, 8, and 18 days, respectively. Lights out resulted in `Lilo' initiating 17 Oct., followed by `Freedom', `Peterstar', and `Success' initiating 7, 12, and 15 days later, respectively. Differences between cultivars in time of initiation was reduced under black cloth, where `Lilo' initiated 14 Oct., followed by `Freedom' 2 days later, and `Peterstar' and `Success' 7 days afterward. Initiation was positively correlated to visible bud and anthesis. First color was positively correlated to initiation and visible bud, with the exception of `Lilo'. Growth room studies conducted using various high temperatures and photoperiods indicated similar trends.


1982 ◽  
Vol 70 (3) ◽  
pp. 898-900 ◽  
Author(s):  
Robert J. Downs ◽  
Judith F. Thomas
Keyword(s):  

2003 ◽  
Vol 128 (4) ◽  
pp. 479-485 ◽  
Author(s):  
Erik S. Runkle ◽  
Royal D. Heins

Plastics that selectively reduce the transmission of far-red light (FR, 700 to 800 nm) reduce extension growth of many floricultural crops. However, FR-deficient (FRd) environments delay flowering in some long-day plants (LDPs), including `Crystal Bowl Yellow' pansy (Viola ×wittrockiana Gams). Our objective was to determine if FR light could be added to an otherwise FRd environment to facilitate flowering with minimal extension growth. In one experiment, plants were grown under a 16-hour FRd photoperiod, and FR-rich light was added during portions of the day or night. For comparison, plants were also grown with a 9-hour photoperiod [short-day (SD) control] or under a neutral (N) filter with a 16-hour photoperiod (long day control). Flowering was promoted most (i.e., percent of plants that flowered increased and time to flower decreased) when FR-rich light was added during the entire 16-hour photoperiod, during the last 4 hours of the photoperiod, or during the first or second 4 hours after the end of the photoperiod. In a separate experiment, pansy was grown under an FRd or N filter with a 9-hour photoperiod plus 0, 0.5, 1, 2, or 4 hours of night interruption (NI) lighting that delivered a red (R, 600 to 700 nm) to FR ratio of 0.56 (low), 1.28 (moderate), or 7.29 (high). Under the N filter, the minimum NI duration that increased percent flowering was 2 hours with a moderate or low R:FR and 4 hours with a high R:FR. Under the FRd filter, 2 or 4 hours of NI lighting with a moderate or low R:FR, respectively, was required to increase percent flowering, but a 4-hour NI with a high R:FR failed to promote flowering. Pansy appears to be day-neutral with respect to flower initiation and a quantitative LDP with respect to flower development. The promotion of reproductive development was related linearly to the promotion of extension growth. Therefore, it appears that in LDPs such as pansy, light duration and quality concomitantly promote extension growth and flowering, and cannot readily be separated with lighting strategies.


HortScience ◽  
1991 ◽  
Vol 26 (6) ◽  
pp. 719A-719
Author(s):  
Richard L. Harkess ◽  
Robert E. Lyons

A study was undertaken to determine the rate of floral initiation in Rudbeckia hirta. R. hirta plants were grown to maturity, 14-16 leaves, under short days (SD). Paired controls were established by placing half of the plants under long days (LD) with the remainder left under SD. Beginning at the start of LD (day 0), five plants were harvested daily from each photoperiod group for twenty days. Harvested meristems were fixed in 2% paraformaldehyde - 2.5% glutaraldehyde in 0.1 M sodium cacodylate buffer (pH 7.0) for 24 hrs, dehydrated in an ethanol series, embedded in paraffin and sectioned at 8 μm. Serial sections were stained with Methyl-green Pyronin, with adjacent sections treated with RNase for nucleic acid comparison. All events of floral initiation were identified, The results of limited inductive photoperiod indicate that 16-18 LD were required for flowering.


1973 ◽  
Vol 21 (4) ◽  
pp. 245-255
Author(s):  
S.J. Wellensiek

Several selected S. armeria lines differing in their reaction to GA3 were treated with GA3 at various concentrations under short-day (SD) or long-day conditions. With SD treatment one application of GA3 at high concentration (10 000 p.p.m. or greater) induced flower formation in certain lines. Stem elongation increased with GA3 concentration and with plant age and was much greater on flowering plants than on non-flowering ones. [For previous related work see HcA 41, 4400.]. (Abstract retrieved from CAB Abstracts by CABI’s permission)


1989 ◽  
Vol 257 (6) ◽  
pp. R1533-R1540 ◽  
Author(s):  
T. J. Bartness ◽  
J. M. Hamilton ◽  
G. N. Wade ◽  
B. D. Goldman

Siberian hamsters exhibit decreased body weight and fat after initial exposure to short photoperiods and increased body weight and fat after extended short photoperiod exposure. The purpose of the present experiments was to determine if uniform changes in white adipose tissue (WAT) pad weights and lipid metabolism correspond to these short photoperiod-induced changes in body fat. Carcass lipid content and testes and fat pad weights [retroperitoneal WAT (RWAT), epididymal WAT (EWAT), and inguinal and dorsal subcutaneous WAT, respectively] were decreased in male hamsters relative to their long day counterparts after 6 and 12 wk of short-day exposure. Moreover, EWAT and RWAT weight, EWAT specific lipoprotein lipase activity, and specific and total lipogenesis were disproportionately decreased relative to the subcutaneous fat pads. The changes in fat pad weight and metabolism were generally reversed coincident with the return to a long-day-like reproductive status after prolonged short-day exposure (24 and 30 wk). In a less detailed experiment, female Siberian hamsters had decreased body, fat pad, and uterine weights after 6 wk of short-day exposure; however, no fat pad-specific changes in weight were observed. The results of these experiments demonstrate that short-day-exposed male Siberian hamsters may be a useful model for examining mechanisms underlying fat pad-specific responses. In addition, gender appears to influence the pattern of short-day-induced lipid depletion in this species.


1984 ◽  
Vol 247 (1) ◽  
pp. R84-R88 ◽  
Author(s):  
J. Dark ◽  
I. Zucker

After 15 wk in a short photoperiod (10 h of light/day), adult male voles weighed 25% less and consumed 33% less food than did voles in a long photoperiod (14 h light/day). Neither body weight nor food intake differed among long- and short-day castrated voles. After 19 wk, castrated long-day voles weighed less than did intact animals. Voles reduced their body weight during the first 15 wk in the short photoperiod and increased their body mass during the succeeding 15 wk. Body mass of short-day voles was positively correlated with combined testes weight. Voles in the short photoperiod collected less nesting material than did their long-day counterparts at week 31. Pelage characteristics at week 32 were not affected by castration or by photoperiod. We conclude that the decreased body mass of male voles during the late summer, fall, and early winter reflects a decrease in circulating levels of testicular hormones; gonadal recrudescence and increased circulating androgen levels are in part responsible for the subsequent seasonal increase in body weight. Part of the increased body mass in late winter in field populations or in laboratory voles after 15 wk in the short photoperiod is independent of the resumption of gonadal activity. Fluctuations in neural and endocrine processes, rather than availability of food, are the principal factors underlying seasonal changes in energy balance.


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