scholarly journals Interactive Effects of Light Quality during Day Extension and Temperature on Bud Set, Bud Burst and PaFTL2, PaCOL1-2 and PaSOC1 Expression in Norway Spruce (Picea abies (L.) Karst.)

Forests ◽  
2021 ◽  
Vol 12 (3) ◽  
pp. 337
Author(s):  
Camilo Chiang ◽  
Marcos Viejo ◽  
Oda Toresdatter Aas ◽  
Katharina T. Hobrak ◽  
Christian Bianchi Strømme ◽  
...  

Light and temperature are crucial factors for the annual growth rhythm of tree seedlings of the boreal and temperate zone. Dormant, vegetative winter buds are formed under short days (SD) and altered light quality. In the conifer Norway spruce, expression of FTL2 increases and PaCOL1-2 and PaSOC1 decrease under light regimes, inducing bud set. Although temperature is known to modulate the timing of bud set, information about combined effects of light climate and temperature on bud phenology and gene expression is limited. We studied the interactive effects of temperature (18, 22/24 °C) and day extension with blue (B), red (R) or far-red (FR) light or different R:FR ratios compared to SD on growth–dormancy cycling and expression of FTL2, PaCOL1-2 and PaSOC1 in Norway spruce seedlings. Day-extension with B light and all treatments involving FR light sustained shoot elongation, with increased growth at higher temperature. The R light treatment resulted in delayed/prevented bud set compared to SD, with more delay/prevented bud set at 24 °C than 18 °C. This was associated with lower PaFTL2-transcript levels at 24 °C and more rapid subsequent bud burst. For the growth-sustaining treatments (long days, FR and B light), the PaFTL2-transcript levels were generally lower and those of PaCO1-2 and PaSOC1 higher compared with SD and R light. In conclusion, our results demonstrate more reduced/prevented bud set and faster bud burst with increased temperature under day extension with R light, indicating less deep dormancy than at lower temperature. Also, sustained shoot elongation under the B light treatment (27 µmol m−2 s−1) in contrast to the lower B light-irradiances tested previously (≤13 µmol m−2 s−1), demonstrates an irradiance-dependent effect of day extension with B light.

2016 ◽  
Vol 121 ◽  
pp. 121-131 ◽  
Author(s):  
Lars Opseth ◽  
Anna Holefors ◽  
Anne Katrine Ree Rosnes ◽  
YeonKyeong Lee ◽  
Jorunn E. Olsen
Keyword(s):  

1988 ◽  
Vol 18 (1) ◽  
pp. 139-142 ◽  
Author(s):  
Rong H. Ho

Black spruce (Piceamariana (Mill.) B.S.P.) grafts growing in a seed orchard were sprayed with gibberellin A4/7, and grafts and trees in families growing in arboreta were sprayed with gibberellin A4/7 and (or) vitamin E from vegetative bud burst to the end of shoot elongation. Gibberellin A4/7 was very effective in promoting seed cones and 400 mg/L appeared optimal. Vitamin E at 1000 mg/L was not effective. Vegetative bud burst occurred in mid-May and shoot elongation ended in late June. Needle primordia were visible on the apices of newly formed buds at the end of June. Reproductive buds had fewer bud scales than vegetative buds. It appeared that potential reproductive buds terminated their bud scale initiation earlier. Gibberellin A4/7 application to promote seed-cone production should be carried out before bud-type differentiation. This coincides with the end of lateral shoot elongation.


2020 ◽  
Vol 61 (5) ◽  
pp. 933-941
Author(s):  
Xiaoying Liu ◽  
Chunmei Xue ◽  
Le Kong ◽  
Ruining Li ◽  
Zhigang Xu ◽  
...  

Abstract We report here the interactive effects of three light qualities (white, red and blue) and three growth temperatures (16�C, 22�C and 28�C) on rosette growth, hypocotyl elongation and disease resistance in Arabidopsis thaliana. While an increase in temperature promotes hypocotyl elongation irrespective of light quality, the effects of temperature on rosette growth and disease resistance are dependent on light quality. Maximum rosette growth rate under white, red and blue light are observed at 28�C, 16�C and 22�C, respectively. The highest disease resistance is observed at 16�C under all three light conditions, but the highest susceptibility is observed at 28�C for white light and 22�C for red and blue light. Interestingly, rosette growth is inhibited by phytochrome B (PHYB) under blue light at 28�C and by cryptochromes (CRYs) under red light at 16�C. In addition, disease resistance is inhibited by PHYB under blue light and promoted by CRYs under red light. Therefore, this study reveals a complex interaction between light and temperature in modulating rosette growth and disease resistance as well as the contribution of PHYB and CRY to disease resistance.


HortScience ◽  
1998 ◽  
Vol 33 (1) ◽  
pp. 75-77 ◽  
Author(s):  
Mark K. Ehlenfeldt

Blueberry cultivars were treated with either soil drenches or foliar applications of paclobutrazol. Soil drenches of 25 mg·L-1 inhibited shoot elongation and stimulated earlier and greater flower bud production on `Bluetta', `Bluecrop', and `Jersey'. The treatments increased bud numbers 359% to 797%, and stimulated compound bud formation, while reducing formation of vegetative buds. This resulted in overcropping and reduced fruit size. Foliar applications at concentrations of 5, 10, 50, and 100 mg·L-1 increased bud set. Treatments did not significantly alter time to 50% flowering in `Bluecrop' or `Duke', but hastened flowering up to 5 days in `Blueray' at 200 ppm. Fruit ripening was significantly delayed at 100 and 200 ppm in `Bluecrop' due to overcropping, but no delays were observed in `Blueray' or `Duke'. Plant size and vigor appeared to be a determining factor in plant response. Chemical name used: PP333 or (2RS,3RS)-l(4-chlorophenyl)-4,4-dimethyl-2-(l,2,4-triazol-1-yl)pentan-3-ol (paclobutrazol).


2006 ◽  
Vol 84 (7) ◽  
pp. 1110-1121 ◽  
Author(s):  
J. Bradley St. Clair

Genetic variation in fall cold damage in coastal Douglas-fir ( Pseudotsuga menziesii (Mirb.) Franco var. menziesii ) was measured by exposing excised branches of seedlings from 666 source locations grown in a common garden to freezing temperatures in a programmable freezer. Considerable variation was found among populations in fall cold hardiness of stems, needles, and buds compared with bud burst, bud set, and biomass growth after 2 years. Variation in fall cold hardiness was strongly correlated (r = 0.67) with cold-season temperatures of the source environment. Large population differences corresponding with environmental gradients are evidence that natural selection has been important in determining genetic variation in fall cold hardiness, much more so than in traits of bud burst (a surrogate for spring cold hardiness), bud set, and growth. Seed movement guidelines and breeding zones may be more restrictive when considering genetic variation in fall cold hardiness compared with growth, phenology, or spring cold hardiness. A regional stratification system based on ecoregions with latitudinal and elevational divisions, and roughly corresponding with breeding zones used in Oregon and Washington, appeared to be adequate for minimizing population differences within regions for growth and phenology, but perhaps not fall cold hardiness. Although cold hardiness varied among populations, within-population and within-region variation is sufficiently large that responses to natural or artificial selection may be readily achieved.


2018 ◽  
Vol 48 (9) ◽  
pp. 1001-1006 ◽  
Author(s):  
Johanna Riikonen

Terminal bud set can be prevented by interrupting night with short pulses of light when the natural photoperiod is too short to maintain growth. Norway spruce (Picea abies Karst.) seedlings originating from 61°N and 64°N were grown in growth chambers under conditions that mimic growth conditions in a heated greenhouse in early spring in Finland (experiment 1) or under constant growth conditions (experiment 2). The seedlings were exposed to the following night interruption (NI) treatments using light-emitting diodes (LEDs) that generated red (R, peak at 660 nm) and far-red (FR, peak at 735 nm) wavelengths in 20 s pulses at 15 min intervals: (i) red light alone (R); (ii) R combined with FR (R + FR); and (iii) control (no NI treatment). The R + FR treatment was more effective in preventing terminal bud set than the R treatment. Seedling responses depended on the provenance and growth conditions. The R treatment reduced the proportion of seedlings with terminal buds in the 61°N seedlings and delayed bud set in the 64°N seedlings. The fluctuating growth conditions or longer dark period between the photoperiod and NI treatments reduced the efficiency of the R + FR treatment. A combination of R and FR LEDs with adequate light intensity and duration is suitable for intermittent NI treatment in Norway spruce seedlings.


2009 ◽  
Vol 29 (11) ◽  
pp. 1457-1465 ◽  
Author(s):  
S. Sutinen ◽  
J. Partanen ◽  
A. Vihera-Aarnio ◽  
R. Hakkinen

1989 ◽  
Vol 19 (8) ◽  
pp. 1051-1058 ◽  
Author(s):  
John N. Owens ◽  
Anna M. Colangeli

Cone buds were induced on container-grown and field-grown western hemlock (Tsugaheterophylla (Raf.) Sarg.) clones during a 3-year period to study the effects of time and duration of gibberellin A4/7 treatment on cone induction, sexuality of cones, and to relate these results to bud and shoot development. The most effective treatment times preceded anatomical differentiation. The most abundant pollen cones and seed cones were produced when trees were sprayed with gibberellin A4/7 before vegetative bud burst and early shoot elongation. Two to three weekly gibberellin A4/7 applications starting at preswollen and swollen-bud stages were adequate for pollen-cone production. Pollen-cone production decreased when the applications were started at vegetative bud burst or during early shoot elongation. A minimum of three weekly applications were required for seed-cone production, and applications were equally effective when started at preswollen, swollen, and vegetative bud burst stages. Seed-cone production decreased when three weekly applications were started during early shoot elongation; however, this was overcome by increasing the number of applications.


Trees ◽  
2004 ◽  
Vol 19 (1) ◽  
pp. 66-72 ◽  
Author(s):  
Jouni Partanen ◽  
Heikki H�nninen ◽  
Risto H�kkinen

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