THE EFFECT OF TEMPERATURE AND PHOTOPERIOD ON INFLORESCENCE DEVELOPMENT IN STRAINS OF TIMOTHY (PHLEUM SPP.)

1958 ◽  
Vol 13 (2) ◽  
pp. 81-91 ◽  
Author(s):  
J. P. Cooper
Botany ◽  
2013 ◽  
Vol 91 (9) ◽  
pp. 642-651 ◽  
Author(s):  
Marlène Antoun ◽  
François Ouellet

Plants adjust their growth and development to ensure survival under adverse environmental conditions. Nonoptimal growth temperatures can have a major impact on biomass and crop yield. A detailed phenotypic analysis (number and length of rosette and cauline branches, flowers, and buds) in Arabidopsis thaliana revealed that growth temperatures below (12 and 17 °C) and above (27 and 32 °C) the control 22 °C affect branching and flowering. The elongation of internodes on the main stem and of primary branches at cauline leaves is reduced at lower temperatures and increased at higher temperatures. Similar results are observed in plants treated before or after bolting. Our data therefore indicate that plants that have transitioned to the reproductive stage before treatment are slightly less affected by temperature variations than plants that are in their vegetative stage. Our results also suggest that plants need to reach a maximum height (internodes length) before they begin forming floral meristems and that this “maximum height” is dependent on the growth temperature. Plants grown at 17 °C show a slightly reduced branching, while those at 27 °C show increased branching. This suggests that apical dominance is a temperature-dependent phenomenon. This is, to our knowledge, the first extensive analysis of the effect of temperature on Arabidopsis inflorescence development.


OENO One ◽  
2019 ◽  
Vol 53 (3) ◽  
Author(s):  
Frederico Alcântara Novelli Dias ◽  
Laurent Torregrosa ◽  
Nathalie Luchaire ◽  
Clea Houel ◽  
Anne Pellegrino

Aim: The success of inflorescence primordia initiation and differentiation within latent buds (i.e. bud fruitfulness) is a critical issue for grapevine yield sustainability under climate change. The aim of the present study was to track the timing and rate of inflorescence development in latent buds along the cane and to quantify their responses to elevated day/night (D/N) temperatures.Methods and Results: The experiments were conducted under controlled conditions, using the microvine model, which is suitable for establishment in small areas. Two imagery methods for analyzing bud anatomy were assessed: light microscopy and x-ray microtomography. Light microscopy was laborious, but it was the most accurate method for investigating organogenesis in the primordial shoot of the latent bud. In plants grown in a greenhouse (D/N, 25°C/15°C), the number of phytomer primordia in latent buds increased linearly from the apical to the basal buds on the cane. A maximum of six phytomers and two inflorescence primordia were observed beneath the 20th bud position that is, slightly fewer than usually reported with macrovines. The first and second inflorescences started to differentiate at the 14th and 18th bud position, respectively. Temperature increases in the growth chamber (D/N, 20–30°C/15–25°C) only slightly changed the final number of preformed phytomers and the probability of inflorescence primordia differentiation per bud. However, elevated temperature sharply accelerated and thereby shortened development of the latent bud primordial shoot, resulting in differentiation of the first inflorescence primordia straight from the fifth bud position. Based on the spatiotemporal conversion of bud position into thermal time, the first inflorescence started to differentiate 332 growing degree days (°Cd) (or 41 days) after bud emergence at D/N 20°C/15°C, and only 98°Cd (or 5 days) after bud emergence at D/N 35°C/25°C. Finally, the number of preformed phytomers was shown to correlate with primary bud length and cane diameter, independent of temperature. These easily measured variables may be used as indicators of bud developmental stage and potential bud fruitfulness in further studies using the microvine.Conclusions: The microvine appears to be suitable for parameterizing a developmental model of grapevine latent buds under controlled environmental conditions and when evaluating the response to elevated D/N temperatures.Significance and impact of the study: The precise description of the timing and rate of differentiation of phytomers and inflorescences opens new perspectives for understanding the molecular processes underlying the response of bud fruitfulness to environmental constraints.


HortScience ◽  
1995 ◽  
Vol 30 (4) ◽  
pp. 862A-862
Author(s):  
James E. Faust ◽  
Royal D. Heins

Axillary buds of African violet develop vegetative shoots or reproductive inflorescences. Vegetative axillary development results in a multiple-shoot plant and reduces plant quality. We determined the effect of temperature and plantlet size on axillary bud development. Plantlets were removed from leaf cuttings, graded according to stem diameter, directly stuck into pots 10 cm in diameter, and placed in greenhouses at 18, 22, or 26C. Vegetative development was related to temperature, plantlet size, and nodal position. The number of vegetative axillary shoots per plant decreased from 3.7 to 1.3; that of leaves per vegetative axillary shoot decreased from 10.3 to 4.8 as temperature increased from 18 to 26C. The eight to 10 basipetal nodes developed vegetative shoots or were devoid of axillary development. The percentage of leaf axils in which inflorescences developed increased from 14 on node eight to 100 on nodes 12 and higher. The larger plantlets at the time of transplant had 20% fewer vegetative axillary shoots, whereas reproductive inflorescence development was not affected by plantlet size.


2000 ◽  
pp. 601-608 ◽  
Author(s):  
N. Sukhvibul ◽  
S.E. Hetherington ◽  
A.W. Whiley ◽  
M.K. Smith ◽  
V. Vithanage

Author(s):  
P. R. Swann ◽  
W. R. Duff ◽  
R. M. Fisher

Recently we have investigated the phase equilibria and antiphase domain structures of Fe-Al alloys containing from 18 to 50 at.% Al by transmission electron microscopy and Mössbauer techniques. This study has revealed that none of the published phase diagrams are correct, although the one proposed by Rimlinger agrees most closely with our results to be published separately. In this paper observations by transmission electron microscopy relating to the nucleation of disorder in Fe-24% Al will be described. Figure 1 shows the structure after heating this alloy to 776.6°C and quenching. The white areas are B2 micro-domains corresponding to regions of disorder which form at the annealing temperature and re-order during the quench. By examining specimens heated in a temperature gradient of 2°C/cm it is possible to determine the effect of temperature on the disordering reaction very precisely. It was found that disorder begins at existing antiphase domain boundaries but that at a slightly higher temperature (1°C) it also occurs by homogeneous nucleation within the domains. A small (∼ .01°C) further increase in temperature caused these micro-domains to completely fill the specimen.


Author(s):  
T. Geipel ◽  
W. Mader ◽  
P. Pirouz

Temperature affects both elastic and inelastic scattering of electrons in a crystal. The Debye-Waller factor, B, describes the influence of temperature on the elastic scattering of electrons, whereas the imaginary part of the (complex) atomic form factor, fc = fr + ifi, describes the influence of temperature on the inelastic scattering of electrons (i.e. absorption). In HRTEM simulations, two possible ways to include absorption are: (i) an approximate method in which absorption is described by a phenomenological constant, μ, i.e. fi; - μfr, with the real part of the atomic form factor, fr, obtained from Hartree-Fock calculations, (ii) a more accurate method in which the absorptive components, fi of the atomic form factor are explicitly calculated. In this contribution, the inclusion of both the Debye-Waller factor and absorption on HRTEM images of a (Oll)-oriented GaAs crystal are presented (using the EMS software.Fig. 1 shows the the amplitudes and phases of the dominant 111 beams as a function of the specimen thickness, t, for the cases when μ = 0 (i.e. no absorption, solid line) and μ = 0.1 (with absorption, dashed line).


1990 ◽  
Vol 80 (3) ◽  
pp. 431-436 ◽  
Author(s):  
Isabelle Delvallee ◽  
Annie Paffen ◽  
Geert-Jan De Klerk

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