Abstract:Phyllotactic diversity and developmental transitions between phyllotactic patterns are not fully understood. The plants studied so far, such as Magnolia, Torreya or Abies, are not suitable for experimental work, and the most popular model plant, Arabidopsis thaliana, does not show sufficient phyllotactic variability. It has been found that in common verbena (Verbena officinalis L.), a perennial, cosmopolitan plant, phyllotaxis differs not only between growth phases in primary transitions but also along the ind… Show more
“…The mean divergence angle of costoid phyllotaxis of this plant in the adult vegetative phase was about 54°. Comparable small divergence angles are found in only few plants outside Costaceae (Rutishauser, 1998; Zagórska-Marek et al, 2021). Picea abies is one of such exceptional plants and was reported to have a divergence angle of 56.4° (Rutishauser, 1998).…”
The view is widely accepted that the inhibitory effect of existing leaf primordia on new primordium formation determines phyllotactic patterning. Previous studies have shown that mathematical models based on such inhibitory effect can generate most of phyllotactic patterns. However, a few types of phyllotaxis still remain unaddressed. A notable example is costoid phyllotaxis showing spiromonostichy, which is characterized by a steep spiral with a small divergence angle and is unique to Costaceae plants. Costoid phyllotaxis has been called a "genuine puzzle" because it seems to disagree with the inhibitory effect-based mechanism. In an attempt to produce a steep spiral pattern, we developed a new mathematical model assuming that each leaf primordium emits not only the inhibitory effect but also some inductive effect. Computer simulations with the new model successfully generated a steep spiral pattern when these two effects met a certain relationship. The obtained steep spiral matched the real costoid phyllotaxis observed with Costus megalobractea. We also found by the mathematical model analysis that the early phyllotactic transition in the seedlings of this plant can be explained by the SAM enlargement.
“…The mean divergence angle of costoid phyllotaxis of this plant in the adult vegetative phase was about 54°. Comparable small divergence angles are found in only few plants outside Costaceae (Rutishauser, 1998; Zagórska-Marek et al, 2021). Picea abies is one of such exceptional plants and was reported to have a divergence angle of 56.4° (Rutishauser, 1998).…”
The view is widely accepted that the inhibitory effect of existing leaf primordia on new primordium formation determines phyllotactic patterning. Previous studies have shown that mathematical models based on such inhibitory effect can generate most of phyllotactic patterns. However, a few types of phyllotaxis still remain unaddressed. A notable example is costoid phyllotaxis showing spiromonostichy, which is characterized by a steep spiral with a small divergence angle and is unique to Costaceae plants. Costoid phyllotaxis has been called a "genuine puzzle" because it seems to disagree with the inhibitory effect-based mechanism. In an attempt to produce a steep spiral pattern, we developed a new mathematical model assuming that each leaf primordium emits not only the inhibitory effect but also some inductive effect. Computer simulations with the new model successfully generated a steep spiral pattern when these two effects met a certain relationship. The obtained steep spiral matched the real costoid phyllotaxis observed with Costus megalobractea. We also found by the mathematical model analysis that the early phyllotactic transition in the seedlings of this plant can be explained by the SAM enlargement.
“…In particular we highlight patterns "outside" Fibonacci patterns and the evolutionary origins of phyllotaxis. Three review articles discussing general aspects (Yin 2021), stochasticities (Kitazawa 2021), and symmetries (Yonekura and Sugiyama 2021); and three original research articles focusing on pattern regeneration (Zhang et al 2021b), a new system for studying phyllotactic transitions (Zagórska-Marek et al 2021), and the origin of phyllotaxis (Kamamoto et al 2021), are included in this special issue.…”
mentioning
confidence: 99%
“…Therefore, to study the diversity of phyllotaxis beyond Fibonacci patterns, a new model system is required. Zagórska-Marek et al (2021) showed that common verbena (Verbena officinalis L.) has preferable features in this regard. This perennial plant is suitable for laboratory experiments, and has phyllotactic transitions not only between growth phases but also within the indeterminate inflorescence axis, without changing the identity of lateral organs.…”
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