@ARTICLE{TreeBASE2Ref19377,
author = {Bruce G. Baldwin and Susan Kalisz and W. Scott Armbruster},
title = {Phylogenetic perspectives on diversification, biogeography, and floral evolution of Collinsia and Tonella (Plantaginaceae)},
year = {2011},
keywords = {California; chromosome evolution; cryptic diversity; endangered species; floral evolution, hybrid speciation; phylogeography; reproductive isolation; Transverse Range break},
doi = {10.3732/ajb.1000346},
url = {http://},
pmid = {},
journal = {American Journal of Botany},
volume = {98},
number = {4},
pages = {731--753},
abstract = {Premise of the study: Collinsia was the subject of classic biosystematic studies by Garber and colleagues and is increasingly investigated to address major evolutionary questions. Lack of phylogenetic data from more than one gene region and one taxonomic exemplar has left relationships, diversity, and phytogeography of Collinsia in question and has limited understanding of its diversification.
Methods: Phylogenetic analyses representing 179 populations of Collinsia and closely related Tonella were conducted based on DNA sequences of nuclear ribosomal transcribed spacers, the chloroplast trnK intron, and the single-copy nuclear gene CYCLOIDEA-1 to reexamine systematic hypotheses and extend understanding of the importance of chromosome evolution, interfertility, crossability, hybridization, edaphic factors, and ecogeographic barriers to diversification in the group.
Key results: Informal ?sections? of Collinsia are artificial, although pedicel length and other traditional deep-level taxonomic characters are more conservative evolutionarily than flower size (and timing of self-pollination). Evolutionary loss of crossability and interfertility in Collinsia appears to be largely a byproduct of divergence. Although most taxa appear to have arisen by divergent evolution, multiple lines of evidence indicate a homoploid hybrid constitution of C. tinctoria, possibly explaining an occurrence of convergent chromosome evolution. Phylogeographic and cryptic diversity are extensive.
Conclusions: Diversity in Collinsia is greater than previously documented. Recently divergent lineages are often associated with distinct habitat (including soil) and geographic factors, different flower sizes, and contrasting chromosomal arrangements. Evidence for a hybrid constitution of diploid C. tinctoria is consistent with lack of strong intersterility barriers between closely related taxa.
}
}
Matrices for Study 11078
Citation title:
"Phylogenetic perspectives on diversification, biogeography, and floral evolution of Collinsia and Tonella (Plantaginaceae)".
Study name:
"Phylogenetic perspectives on diversification, biogeography, and floral evolution of Collinsia and Tonella (Plantaginaceae)".
This study is part of submission 11068
(Status: Published).
Matrices
ID |
Matrix Title |
Description |
Data type |
NTAX |
NCHAR |
Taxa |
|
|
|
|
M7302
|
Collinsia CYC1 matrix |
Collinsia CYCLOIDEA-1 |
Nucleic Acid |
47 |
1029 |
View Taxa
|
|
|
|
|
M7303
|
Collinsia nrDNA+cpDNA matrix |
Collinsia nrDNA ITS+ETS & cpDNA 3'matK+3'trnK intron |
Nucleic Acid |
148 |
1576 |
View Taxa
|
|
|
|
|
M7301
|
Collinsia cpDNA matrix |
Collinsia 3' matK gene + 3' trnK intron |
Nucleic Acid |
61 |
524 |
View Taxa
|
|
|
|
|
M7298
|
Collinsia nrDNA matrix |
Collinsia ITS region + 3' end of ETS (upstream of 18S) |
Nucleic Acid |
139 |
1052 |
View Taxa
|
|
|
|
|
M7297
|
Collinsia all-partitions |
Collinsia nrDNA, cpDNA & CYCLOIDEA-1 |
Nucleic Acid |
29 |
2534 |
View Taxa
|
|
|
|
|