» Articles » PMID: 22318659

Ecological Segregation Drives Fine-scale Cytotype Distribution of Senecio Carniolicus in the Eastern Alps

Overview
Journal Preslia
Date 2012 Feb 10
PMID 22318659
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

In order to uncover patterns and processes of segregation of co-existing cytotypes, we investigated a zone in the eastern Alps (Austria) where diploid and hexaploid individuals of the alpine herb Senecio carniolicus Willd. (Asteraceae) co-occur. Linking the fine-scale distribution of cytotypes to environmental and spatial factors revealed segregation along an ecological gradient, which was also reflected in the cytotype-associated plant assemblages. Compared to diploids, hexaploids are found in more species-rich and denser communities. This may be due to their better competitive ability and lower tolerance of abiotic stress compared to the diploids. The lack of any intermediate cytotypes suggests the presence of strong reproductive isolation mechanisms, whose nature is, however, elusive.

Citing Articles

The Use of Flow Cytometry for Estimating Genome Sizes and DNA Ploidy Levels in Plants.

Loureiro J, certner M, Lucanova M, Sliwinska E, Kolar F, Dolezel J Methods Mol Biol. 2023; 2672:25-64.

PMID: 37335468 DOI: 10.1007/978-1-0716-3226-0_2.


Temporal stability of spatial cytotype structure in mixed-ploidy populations of .

Mraz P, Spaniel S, Skokanova K, Singliarova B AoB Plants. 2022; 14(6):plac052.

PMID: 36439406 PMC: 9683110. DOI: 10.1093/aobpla/plac052.


Variation in heteroploid reproduction and gene flow across a polyploid complex: One size does not fit all.

Sutherland B, Galloway L Ecol Evol. 2021; 11(14):9676-9688.

PMID: 34306653 PMC: 8293777. DOI: 10.1002/ece3.7791.


Role of ploidy in colonization of alpine habitats in natural populations of Arabidopsis arenosa.

Wos G, Morkovska J, Bohutinska M, Sramkova G, Knotek A, Lucanova M Ann Bot. 2019; 124(2):255-268.

PMID: 31185073 PMC: 6758580. DOI: 10.1093/aob/mcz070.


Pollen precedence in sexual and its role as a protective reproductive barrier against apomictic cytotypes.

Alonso-Marcos H, Hulber K, Myllynen T, Perez Rodriguez P, Dobes C Taxon. 2019; 67(6):1132-1142.

PMID: 30745710 PMC: 6368848. DOI: 10.12705/676.9.


References
1.
Baack E, Stanton M . Ecological factors influencing tetraploid speciation in snow buttercups (Ranunculus Adoneus): niche differentiation and tetraploid establishment. Evolution. 2005; 59(9):1936-44. View

2.
Meirmans P, Vlot E, DEN Nijs J, Menken S . Spatial ecological and genetic structure of a mixed population of sexual diploid and apomictic triploid dandelions. J Evol Biol. 2003; 16(2):343-52. DOI: 10.1046/j.1420-9101.2003.00515.x. View

3.
Soltis D, Albert V, Leebens-Mack J, Bell C, Paterson A, Zheng C . Polyploidy and angiosperm diversification. Am J Bot. 2011; 96(1):336-48. DOI: 10.3732/ajb.0800079. View

4.
Halverson K, Heard S, Nason J, Stireman 3rd J . Origins, distribution, and local co-occurrence of polyploid cytotypes in Solidago altissima (Asteraceae). Am J Bot. 2011; 95(1):50-8. DOI: 10.3732/ajb.95.1.50. View

5.
Suda J, Travnicek P . Reliable DNA ploidy determination in dehydrated tissues of vascular plants by DAPI flow cytometry--new prospects for plant research. Cytometry A. 2006; 69(4):273-80. DOI: 10.1002/cyto.a.20253. View