@ARTICLE{TreeBASE2Ref17284,
author = {L. R?ber and Ralf Britz and Rafael Zardoya},
title = {Molecular phylogenetics and evolutionary diversification of labyrinth fishes (Perciformes; Anabantoidei)},
year = {2006},
keywords = {},
doi = {10.1080/10635150500541664},
url = {},
pmid = {},
journal = {Systematic Biology},
volume = {55},
number = {3},
pages = {374--397},
abstract = {Labyrinth fishes (Perciformes: Anabantoidei) are primary freshwater fishes with a disjunct African-Asian distribution that exhibit a wide variety of morphological and behavioral traits. These intrinsic features make them particularly well suited for studying patterns and processes of evolutionary diversification. We reconstructed the first molecular-based phylogenetic hypothesis of anabantoid intrarelationships using both mitochondrial and nuclear nucleotide sequence data to address anabantoid evolution. The mitochondrial data set included the complete cytochrome b, partial 12S rRNA, complete tRNA Val, and partial 16S rRNA genes (3340 bp) of 57 species representing all 19 anabantoid genera. The nuclear data set included the partial RAG1 gene (1473 bp) of 21 representative species. The phylogenetic analyses of a combined (mitochondrial + nuclear) data set recovered almost fully resolved trees at the intrafamily level with different methods of phylogenetic inference. Phylogenetic relationships at this taxonomic level were compared with previous morphology-based hypotheses. In particular, the enigmatic pike-head (Luciocephalus) was confidently placed within the ?spiral egg? clade, thus resolving the long-standing controversy on its relative phylogenetic position. The molecular phylogeny was used to study the evolution of the different forms of parental care within the suborder. Our results suggest that the evolution of breeding behavior in anabantoids is highly correlated with phylogeny, and that brood care evolved three times independently from an ancestral free spawning condition without parental care. Ancestral character state reconstructions under maximum parsimony and maximum likelihood further indicated that both bubble nesting and mouthbrooding have evolved recurrently during anabantoid evolution. The new phylogenetic framework was also used to test alternative biogeographic hypotheses that account for the disjunct African ? Asian distribution. Molecular divergence time estimates support either a drift vicariance linked to the breakup of Gondwana or Late Mesozoic Early Tertiary dispersal from Africa to Asia. [ancestral character state reconstruction; breeding behavior; divergence time estimation; biogeography]}
}
Matrix 1014 of Study 1464

Citation title:
"Molecular phylogenetics and evolutionary diversification of labyrinth fishes (Perciformes; Anabantoidei)".

This study was previously identified under the legacy study ID S1403
(Status: Published).
Matrices
Title: combined 24
Description: Legacy TreeBASE Matrix ID = M2520
Rows
|
Taxon Label |
Row Segments |
Characters 1?–30 |
| Parachanna obscura |
(none)
|
ATGGCAAGCCTACGAAAAACCCGCCCCCTC |
| Channa marulia |
(none)
|
ATGGCAAACCTACGAAAAACACACCCCCTC |
| Channa bleheri |
(none)
|
ATGGCAAGCCTACGAAAAACTCACCCGCTC |
| Microctenopoma fasciolatum |
(none)
|
ATGGCCCCCCTACGAAAAGCCCATCCACTC |
| Ctenopoma muriei |
(none)
|
ATGGCTAGCCTACGAAAAACTCACCCCCTT |
| Ctenopoma petherici |
(none)
|
ATGACCCATCTACGAAAAACCCACCCCCTC |
| Ctenopoma pellegrini |
(none)
|
ATGGCCAACCTACGAAAAACCCACCCCCTA |
| Sandelia capensis |
(none)
|
ATGGCTAGCCTACGAAAAACCCACCCCCTA |
| Anabas testudineus |
(none)
|
ATGGCCAACATCCGAAAAACCCACCCATTA |
| Helostoma temminkii |
(none)
|
ATGGCGAATTTACGTAAAAATCACCCCCTC |
| Belontia hasselti |
(none)
|
ATGGCAAATCTACGAAAAACCCACCCCCTC |
| Osphronemus gouramy |
(none)
|
ATGGCAAACCTACGAAAAACCCACCCCCTT |
| Luciocephalus pulcher |
(none)
|
ATGGCAAACCTACGAAAATCCCACCCCCTT |
| Sphaerichthys osphromenoides |
(none)
|
ATGGCAAATCTACGAAAATCGCACCCACTC |
| Parasphaerichthys ocellatus |
(none)
|
ATGGCAAACCTACGAAAATCTCACCCCTTA |
| Ctenops nobilis |
(none)
|
ATGGCCAACCTACGAAAAACCCACCCCTTA |
| Colisa chuna |
(none)
|
ATGGCAAATCTACGAAAAACCCACCCCCTT |
| Trichogaster leerii |
(none)
|
ATGGCAAACATACGAAAAACTCACCCCCTC |
| Betta splendens |
(none)
|
ATGACCCACCAACGTAAAAATCACCCACTA |
| Trichopsis vittata |
(none)
|
ATGGCAAGCCTACGAAAAGAACACCCAATC |
| Parosphromenus deissneri |
(none)
|
ATGACAAACTTACGAAAAACCCACCCACTC |
| Malpulutta kretseri |
(none)
|
ATGGCAAGTCTACGAAAAACACACCCCTTG |
| Pseudosphromenus cupanus |
(none)
|
ATGGCAAGTCTCCGAAAGAAGCATGTTGTA |
| Macropodus opercularis |
(none)
|
ATGGCAAACCTACGAAAAACCCATCCCTTA |
Columns
None of the columns has a description.