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. 2022 Jun 14:3:e13.
doi: 10.1017/qpb.2022.10. eCollection 2022.

Fibonacci spirals may not need the Golden Angle

Affiliations

Fibonacci spirals may not need the Golden Angle

Xiaofeng Yin et al. Quant Plant Biol. .

Abstract

Phyllotaxis, the regular arrangement of plant lateral organs, is an important aspect of quantitative plant biology. Some models relying on the geometric relationship of the shoot apex and organ primordia focus mainly on spiral phyllotaxis, a common phyllotaxis mode. While these models often predict the dependency of Fibonacci spirals on the Golden Angle, other models do not emphasise such a relation. Phyllotactic patterning in Asteraceae is one such example. Recently, it was revealed that auxin dynamics and the expansion and contraction of the active ring of the capitulum (head) are the key processes to guide Fibonacci spirals in gerbera (Gerbera hybrida). In this Insights paper, we discuss the importance of auxin dynamics, distinct phases of phyllotactic patterning, and the transition of phyllotaxis modes. These findings signify the local interaction among primordia in phyllotactic patterning and the notion that Fibonacci spirals may not need the Golden Angle.

Keywords: auxin; capitulum; parastichy; pattern transition; phyllotaxis.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

None
Graphical abstract
Fig. 1.
Fig. 1.
Key patterning processes in gerbera (Gerbera hybrida) capitula development. (a) A capitulum (head) of G. hybrida with outer bracts and inner florets. Pink spiral, one out of 21 clockwise parastichies. Blue spiral, one out of 34 counter-clockwise parastichies. Note that 21 and 34 are two successive numbers of Fibonacci series. White lines, divergence angle of two florets. (b) Confocal images of DR5 reporter indicating that, at the beginning of the patterning process, auxin maxima emerge at approximately the same radial distance from a few discrete steps. (c) Details of DR5 patterning of a newly emerged maximum. The new maximum (P9) moves laterally towards its older neighbour (P1). (d) Predicted distribution of bract primordia (coloured dots) overlaid on confocal images of DR5 reporter. (e) Quantification of DR5 signal intensity in the same region as in (c). (f) Confocal images of DR5 reporter indicating that, as the patterning process continues, auxin maxima emerge closer to the centre. (g) Zigzag-like pattern front formed by initially emerged auxin maxima (on the white circle) and later emerged auxin maxima (on the red circle). Note the slight size difference between the white and the red circle. (h) A schematic diagram showing the lateral movement of auxin maxima. As a result, a long (L) gap and a short (S) gap are generated. Note that the lateral movement is always towards the older neighbour. White numbers in (b,f) and numbers in (h) indicate only positions and do not imply the order of emergence; yellow numbers in (b,d,f,g) indicate the total number of auxin maxima. (a) Modified from Elomaa (2017). (b–g) Modified from Zhang et al. (2021). (h) Derived from Zhang (2021).

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