Within population genetic differentiation in traits affecting clonal growth: Festuca rubra in a mountain grassland

• Published in: Journal of evolutionary biology Vol. 10; no. 3; pp. 383 - 406
• Main Authors: Skálová, H., Pecháčková, S., Suzuki, J., Herben, T., Hara, T., Hadincová, V., Krahulec, F.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Science Ltd 01.05.1997
• Subjects: Festuca rubra; Foraging; plasticity; reaction norms; red/far red ratio; rhizome architecture; spatial spreading; tillering; tussock architecture
• ISSN: 1010-061X; 1420-9101
• DOI: 10.1046/j.1420-9101.1997.10030383.x

Festuca rubra , a clonal grass of mountain grasslands, possesses a considerable variability in traits related to spatial spreading (rhizome production, length and branching; tussock architecture). Since these traits highly influence the success of the species in a spatially heterogeneous system of grasslands, a combined field and growth chamber approach was adopted to determine the within‐population variation in these parameters. Clones were sampled in a mountain grassland (The Krkonoše Mts., Czech Republic); the environment (mean neighbour density) of individual clones varied highly. Before the clones were collected, shoot demography and tussock architecture within these clones were recorded in the field for four seasons. Their clone identity was determined using DNA RAPD. Vegetatively propagated plants from these clones were cultivated in a common garden experiment to demonstrate variation in tussock growth and architecture. Their response to change in red/far red light ratio was determined in the growth chamber. Highly significant variation among clones was found in almost all parameters. In the common garden, the clones differed in tussock growth (mean tillering rate), architecture (mean shoot angle, mean tussock density) and proportion of flowering shoots. In the growth chamber, both the aboveground parameters and parameters of the rhizome system were strongly affected by red/far red ratio; among‐clone variation was also almost always significant. The genotype × environment interaction was significant for tillering rate and rhizome architecture. The structure of the rhizome system (which is the major component of clonal spread in space) is a complex result of several components whose inter‐clone variations differ: (i) genetically determined mean rhizome system size, (ii) overall plasticity in rhizome system size (with no significant genetic variation in plasticity), and (iii) genetically determined plasticity in rhizome architecture. Because of the variation in plasticity in rhizome architecture, some c lones seemed to possess the ability to exploit a favourable habitat patch by producing short branches when there; whereas the remaining clones appeared to possess only a simple escape mechanism from unfavourable patches. Environmental variation in the light levels in the studied grassland is fine grained; horizontal growth rates of F. rubra are sufficient to make genets experience different patches in their lifetime. The high variation in both genotype means and plasticities is likely to be due to selection early in genet life in an environment which is heterogeneous at a fine scale.