scholarly journals Growing competitive or tolerant? Significance of apical dominance in the overcompensating herb Gentianella campestris

Ecology ◽  
2018 ◽  
Vol 99 (2) ◽  
pp. 259-269 ◽  
Author(s):  
Tommy Lennartsson ◽  
Satu Ramula ◽  
Juha Tuomi
2000 ◽  
Vol 14 (4-6) ◽  
pp. 373-392 ◽  
Author(s):  
Ari-Pekka Huhta ◽  
Tommy Lennartsson ◽  
Juha Tuomi ◽  
Pasi Rautio ◽  
Kari Laine

2012 ◽  
Vol 158 (4) ◽  
pp. 2053-2067 ◽  
Author(s):  
Paula Teper-Bamnolker ◽  
Yossi Buskila ◽  
Yael Lopesco ◽  
Shifra Ben-Dor ◽  
Inbal Saad ◽  
...  

1973 ◽  
Vol 51 (6) ◽  
pp. 1137-1145 ◽  
Author(s):  
Kyu-Byung Yun ◽  
J. M. Naylor

The mitotic cycle can be arrested in the apical summit of vegetative terminal buds of Tradescantia paludosa by restricting the level of nitrogen or light available to the plant. Cells in this portion of the bud are much more sensitive to these stress conditions than those in the subjacent portion of the meristem. This differential response induced the establishment of a quiescent "central zone" which is distinguished from the rest of the meristem by the apparent absence of mitosis and DNA synthesis, larger nuclear volume, and a lower histone content of chromatin. These features are identical with those imposed by apical dominance in apices of inhibited lateral buds.The results support the view that competition for nutrients is an important causal factor in apical dominance. They suggest also that competition for nutrients within the terminal bud meristem is important in the regulation of growth in vegetative shoots in respones to conditions of the environment.


2006 ◽  
Vol 84 (1) ◽  
pp. 143-150 ◽  
Author(s):  
Stephen P. Bonser ◽  
Lonnie W. Aarssen

Generalisations of life histories in plants are often framed in terms of allocation to reproduction. For example, relative allocation to reproduction is commonly found to be higher in semelparous than in iteroparous plant species. However, the association between vegetative traits and life history has been largely unexplored. In higher plants, reproductive and vegetative function can be measured in terms of meristem allocation. Under this approach, two vegetative traits (apical dominance (the suppression of axillary meristem development) and branching intensity (the commitment of axillary meristems to branches)) can be measured as well as one reproductive trait (reproductive effort). We used phylogenetically independent contrasts to compare reproductive and vegetative function in annual semelparous and perennial iteroparous species. Twenty congeneric species pairs (each species pair represented by one semelparous and one iteroparous species) across nine families were selected based on availability of herbarium specimens. Semelparous life-history evolution was associated with higher reproductive effort. Conversely, iteroparous life-history evolution was associated with higher apical dominance. Branching intensity was not associated with life history. An evolutionary association between life history and apical dominance but not branching intensity suggests a complex relationship between allocation to vegetative traits and the evolution of plant strategies across environments.


2000 ◽  
Vol 78 (5) ◽  
pp. 591-599 ◽  
Author(s):  
Ari-Pekka Huhta ◽  
Juha Tuomi ◽  
Pasi Rautio

Apical dominance is advantageous in conditions favoring rapid growth in height and unbranched architecture. The cost of apical dominance, on the other hand, should be expressed in conditions where fecundity increases along with an increasing number of branches. Apical damage can be used to measure such costs: when suppressed meristems are released from apical inhibition, the vegetative and reproductive productivity of initially unbranched plants should increase owing to the regrowth and increased branch development following damage. We studied these regrowth responses in two monocarpic herbs, Erysimum strictum P. Gaertn., B. Mey., and Scherb. and Rhinanthus minor L., after both apical damage (10% of the shoot cut) and more extensive damage (50 and 75% cutting). Both species tolerated apical damage, although severe damage had detrimental effects on the performance of both, especially R. minor. Apical damage had positive effects on most of the measured performance parameters of Erysimum. However, the success of seed germination collapsed, presumably due to delayed flowering and less successful pollination. The response was parallel in Rhinanthus; apical damage affected neither the vegetative biomass nor fecundity, but heavier damage, especially 75% clipping, led to severe reductions in most performance measures. The differences in regrowth responses are presumably due to the different habitat requirements of the species. Rhinanthus prefers relatively dense vegetation and starts to branch and produce flowers after a certain threshold in height has been reached, whereas Erysimum prefers gaps in vegetation. In this species, unbranched architecture may be favored in closed vegetation and branched architecture in less competitive habitats. In both species, fruit production correlated positively with the number of branches in both control and clipped plants, which is consistent with the assumption of the cost of apical dominance.Key words: apical dominance, competition, damage, meristem, overcompensation, regrowth.


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