The long-short day requirement for flowering in Stylosanthes guianensis

1988 ◽  
Vol 39 (2) ◽  
pp. 199 ◽  
Author(s):  
K Trongkongsin ◽  
LR Humphreys

Five 'tardio' selections of Stylosanthes guianensis ssp. guiunensis var. pauciflora and S. guiunensis var. guianensis cv. Cook were grown in a glasshouse where natural daylength was shortencd, or extended by incandescent lamps. They did not flower or flowered weakly in 152 cycles of 10 h short days (SD), but flowered more rapidly and prolifically if exposed to 30, 60 or 90 16 h long days (LD) followed by 30 10 h cycles than under natural daylength conditions at 27' 30' S. Increasing the previous exposure to LD reduced the number of 10 h cycles to floral initiation. Similar behaviour was exhibited by cv. Bandeirante which did not flower in 131 cycles of 11 h, but which flowered when SD induction followed 45 to 65 cycles of 14 h. Spike density was positively related to number of LD, which favoured first flower appearance on the terminal apices of lateral rather than of main shoots. CIAT 1283 and cv. Cook grown in controlled environment cabinets at 30�/23� (day/night) did not flower in 140 cycles of 10 h SD, but flowered if LD were interposed before SD induction. Cook had a greater LD requirement of 50 cycles of 14 or 15.5 h for floral initiation, whilst CIAT 1283 had a lesser LD requirement and flowered after 20 cycles of 14 or 15.5 h or after 50 cycles of 12.5 h. These data indicate a qualitative long-short day flowering response. This has implications which favour the higher latitudes for seed production and the early summer sowing of seed crops when plants would receive maximum LD exposure before SD induction occurs.

1984 ◽  
Vol 35 (2) ◽  
pp. 219 ◽  
Author(s):  
RL Ison ◽  
LR Humphreys

Seedlings of Stylosanthes guianensis var. guianensis cv. Cook and cv. Endeavour were grown in naturally lit glasshouses at Brisbane (lat. 27� 30' S.) at 35/30, 30/25 and 25/20�C (day/night), and were sown so as to emerge at 18-day intervals from 18 January to 11 June. Cook behaved as a long day-short day plant, with seedlings emerging after 5 February flowering incompletely or remaining vegetative until the experiment was terminated in mid-October. In the 25/20�C regimen flowering was incomplete in Cook; in Endeavour flowering was delayed but a conventional short-day response was observed. At 35/30�C Endeavour flowering was inhibited in the shortest days of mid-winter, suggesting a stenophotoperiodic response, but short days were confounded with low levels of irradiance. Minimum duration of the phase from emergence to floral initiation was c. 66-70 days in Cook and c. 40-45 days in Endeavour; the duration of the phase floral initiation to flower appearance was linearly and negatively related to temperature.


1973 ◽  
Vol 51 (3) ◽  
pp. 535-551 ◽  
Author(s):  
Marje Molder ◽  
John N. Owens

Plants of Cosmos bipinnatus Cav. ‘Sensation’ (a quantitative short-day plant) were grown under continuous conditions favorable or unfavorable for flowering, and some plants in each group were treated with gibberellic acid (GA3). Floral apices of Cosmos are formed by the transition of previously vegetative apices. The vegetative apex shows a cytohistological zonation pattern superimposed upon a tunica–corpus organization. The vegetative apex passes into an intermediate stage presumed typical of many plants held under non-inductive conditions. This stage is marked by many cytological features characteristic of both reproductive and vegetative apices but leaves continue to be produced. The presence of the intermediate stage accounts for conflicting results obtained in physiological studies since there is great variation in response rate depending on age of plant and the stage of the apex at the start of an experiment. This stage is followed by a typical transitional stage marked by an increase in RNA content, increased mitotic activity, and a change in zonation. Elongation of the apex and internodes occurs followed by initiation of the involucral bracts and floret primordia, marking the beginning of the prefloral and inflorescence stages respectively.GA3 specifically induces Cosmos to flower under non-inductive conditions thereby influencing floral initiation in a facultative short-day plant. Microscopic examination of the rate of apical transition revealed that GA3 substituted effectively for short days but was not as efficient an inducer as were short days.


HortScience ◽  
1992 ◽  
Vol 27 (1) ◽  
pp. 73-74
Author(s):  
G.L. Roberts ◽  
M.J. Tsujita ◽  
J. Gerrath

Sisyrinchium bemudiana L. plants were grown in growth chambers under lo-hour short-day regimes. Scanning electron microscopy of shoot apices collected at biweekly intervals showed that the transition from vegetative to floral status occurs after 10 weeks of short days. Stamens and tepals develop first as common stamentepal primordia that then bifurcate to form outer tepals with stamens opposite. Subsequently, the inner tepals are initiated in an alternate pattern.


1970 ◽  
Vol 21 (3) ◽  
pp. 383 ◽  
Author(s):  
NJ Halse ◽  
RN Weir

Sixteen Australian wheat cultivars grown in controlled environment cabinets demonstrated a range of responses to seed vernalization varying from little or no promotion of floral initiation in Darkan, Kondut, Falcon, and Sunset to about 3 weeks in Festiguay, Claymore, and Mexico 120. Under short days (10 hr photoperiod v. 14 hr) or cold temperatures (12/7�C day/night v. 18/13�) the response to seed vernalization was reduced. None of the cultivars responsive to vernalization achieved floral initiation earlier under cold temperatures than under warm temperatures, even in the absence of seed vernalization. All cultivars achieved floral initiation earlier in long days but the magnitude of the response varied considerably among them. Long days similarly accelerated development from initiation to anthesis. Higher temperatures accelerated development to initiation and anthesis in all cultivars, with only minor differences in magnitude of response. Selected treatments in the cabinets gave rates of development to initiation which closely paralleled results for the same cultivars in field experiments. The number of spikelets per head varied considerably with cultivar, day length, and vernalization treatment. Within the range of conditions of the experiments, temperature did not affect spikelet number other than through vernalization. At either temperature, the spikelet number was closely and positively related to the number of days to floral initiation.


HortScience ◽  
1997 ◽  
Vol 32 (6) ◽  
pp. 1044-1045 ◽  
Author(s):  
Richard A. Criley ◽  
William S. Sakai

Seasonal flowering behavior of Heliconia wagneriana Petersen was found to be caused by short daylengths (SD) using artificial short days (8 to 9 hours) and long days as daylength extension or night break lighting with incandescent lamps. The natural time for flower initiation was estimated to be mid- to late October (11 hours 40 minutes to 11 hours 20 minutes) in Hawaii, and 120 to 150 days were required from the onset of inductive SD to inflorescence emergence. The results may be used to manipulate flower availability for flower markets.


1985 ◽  
Vol 12 (3) ◽  
pp. 291 ◽  
Author(s):  
RL Ison

Mature plants of the tropical legume Stylosanthes guianensis var. guianensis cv. Schofield required 20 short-day (SD) cycles (of 10-h days) for irrevocable commitment to floral initiation when returned to natural long days (LD), although the morphological changes associated with floral initiation were evident after 12-18 SD cycles. Commitment to flowering and spike production were favoured by 20 or more SD cycles. Floret number per spike and percentage seed set were not affected by return to LD. Within individual plants, sections of terminal and branch apices revealed a range of development stages. Terminal apices of well developed lateral branches were able to initiate as soon as, or sooner than, terminal apices of the main branch in this usually determinate plant; this points to individual branches having some autonomy for floral initiation, but suggests dissections made from well developed lateral branches would be a feasible method for determining floral initiation where plant replication is limited.


1986 ◽  
Vol 16 (5) ◽  
pp. 949-954 ◽  
Author(s):  
D. E. Macey ◽  
J. T. Arnott

Piceaglauca (Moench) Voss seedlings were grown in controlled environment rooms following germination with a combination of fluorescent and incandescent lamps (ratio, 1.4:1) providing 390 μmol s−1 m−2 of photosynthetically active radiation over a 24-h photoperiod. Moderate moisture and nutrient stress treatments were applied to separate seedling groups (10 weeks from germination) for a 2-week period during the initial free growth phase when mean seedling shoot length had reached 12 cm. Photoperiod was then reduced to 8 h. Both periodic moisture stress (reaching −1.72 MPa) and nutrient withdrawal (N, P, K) were effective in inducing terminal bud formation in container-grown white spruce seedlings under nonlimiting photoperiod and the number of needle primordia subsequently formed in the terminal bud under short days was significantly reduced. However, decreased needle complements in the stressed seedlings did not result in reduced shoot growth in the second growing season. Free growth following extension of the preformed shoot compensated for the reduced amount of predetermined foliage.


Author(s):  
Nour Nissan ◽  
Elroy R. Cober ◽  
Michael Sadowski ◽  
Martin Charette ◽  
Ashkan Golshani ◽  
...  

Abstract Key message A previously identified soybean maturity locus, E6, is discovered to be J, with the long juvenile allele in Paranagoiana now deemed j−x. Abstract Soybean grown at latitudes of ~20° or lower can produce lower grain yields due to the short days. This limitation can be overcome by using the long juvenile trait (LJ) which delays flowering under short day conditions. Two LJ loci have been mapped to the same location on Gm04, J and E6. The objective of this research was to investigate the e6 allele in ‘Paranagoiana’ and determine if E6 and J are the same locus or linked loci. KASP markers showed that e6 lines did not have the j−1 allele of LJ PI 159925. A population fixed for E1 but segregating for E6, with e6 introgressed from Paranagoiana, showed single gene control for flowering and maturity under short days. Sequencing Glyma.04G050200, the J gene, with long amplification Taq found that the e6 line ‘Paranagoiana’ contains a Ty1-copia retrotransposon of ~10,000 bp, inserted within exon 4. PCR amplification of the cDNA of Glyma.04G050200 also showed differences between the mRNA sequences (presence of insertion in j−x). Hence, we conclude that the loci E6 and J are one locus and deem this new variation found in Paranagoiana as j−x.


1988 ◽  
Vol 24 (2) ◽  
pp. 237-245
Author(s):  
Serpil Terzioğlu

SUMMARYThe vernalization and photoperiodic response of six locally adapted bread wheat cultivars grown under natural daylength conditions during the summer or winter months was examined in glasshouse experiments. The wheat was vernalized by chilling imbibed grains at 2 ± 1°C for 0, 15 or 45 days. Vernalization for 45 days followed by long summer days led to floral initiation in all cultivars within 28 days but vernalization for 0 or 15 days only led to floral initiation in one cultivar. Vernalization followed by long days reduced the time from transplanting to anthesis, resulting in early ear emergence. Vernalization followed by short days accelerated the development of all the cultivars, but normal development could also occur without vernalization at this time of year. Apical differentiation of the primary shoot and its length and development gave the most reliable information on the period of vernalization required.


1966 ◽  
Vol 14 (2) ◽  
pp. 89-102
Author(s):  
T.A. Hartman

In vernalization trials with winter rye, short-day treatment prior to cold treatment was capable of inducing accelerated development and early ear emergence even when the temperature during the former treatment was 25 degrees C. Short days imposed during protracted cold treatments could also accelerate development provided that the optimum duration of short-day vernalization (about 14 days) was not exceeded. Results confirmed the assumption that cold vernalization and short-day vernalization were different processes. [See also F.C.A. 18: 1236].-R.B. (Abstract retrieved from CAB Abstracts by CABI’s permission)


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