@ARTICLE{TreeBASE2Ref17442,
author = {James Allen Schulte II and K. d. Queiroz},
title = {Phylogenetic Relationships and Heterogeneous Evolutionary Processes among Phrynosomatine Sand Lizards (Squamata, Iguanidae) Revisited},
year = {2007},
keywords = {},
doi = {},
url = {},
pmid = {},
journal = {Molecular Phylogenetics and Evolution},
volume = {},
number = {},
pages = {},
abstract = {Phylogenetic analyses of DNA sequences were conducted to evaluate four alternative hypotheses of phrynosomatine sand lizard relationships. Sequences comprising 2871 aligned base pair positions representing the regions spanning ND1-COI and cyt b-tRNAThr of the mitochondrial genome from all recognized sand lizard species were analyzed using unpartitioned parsimony and likelihood methods, likelihood methods with assumed partitions, Bayesian methods with assumed partitions, and Bayesian mixture models. The topology (Uma, (Callisaurus, (Cophosaurus, Holbrookia))) and thus monophyly of the earless taxa, Cophosaurus and Holbrookia, is supported by all analyses. Previously proposed topologies in which Uma and Callisaurus are sister taxa and those in which Holbrookia is the sister group to all other sand lizard taxa are rejected using both parsimony and likelihood-based significance tests with the combined, unparitioned data set. Bayesian hypothesis tests also reject those topologies using six assumed partitioning strategies, and the two partitioning strategies presumably associated with the most powerful tests also reject a third previously proposed topology, in which Callisaurus and Cophosaurus are sister taxa. For both maximum likelihood and Bayesian methods with assumed partitions, those partitions defined by codon position and tRNA stem and nonstems explained the data better than other strategies examined. Bayes factor estimates comparing results of assumed partitions versus mixture models suggest that mixture models perform better than assumed partitions when the latter were not based on functional characteristics of the data, such as codon position and tRNA stem and nonstems. However, assumed partitions performed better than mixture models when functional differences were incorporated. We reiterate the importance of accounting for heterogeneous evolutionary processes in the analysis of complex data sets and emphasize the importance of implementing mixed model likelihood methods.}
}
Taxa for matrix 4283 of Study 1954

Citation title:
"Phylogenetic Relationships and Heterogeneous Evolutionary Processes among Phrynosomatine Sand Lizards (Squamata, Iguanidae) Revisited".

This study was previously identified under the legacy study ID S1936
(Status: Published).
Taxa
Return to matrix row view
| ID |
Taxon Label |
NCBI taxid |
uBIO namebankID |
| 249617 |
Botryosphaeria rhodina |
45133
|
3189934
|
| 249604 |
Chalaropsis sp. |
|
|
| 249598 |
Cladosporium aff. cladosporioides |
|
|
| 249611 |
Cladosporium sp. A35 |
|
|
| 249606 |
Cladosporium sp. A40 |
|
|
| 249576 |
Colletogloeopsis considenianae |
407941
|
10325767
|
| 249584 |
Kirramyces sp. |
|
|
| 249592 |
Kirramyces sp. EU009626 |
|
|
| 249567 |
Kirramyces sp. EU301005 |
|
|
| 242649 |
Mycosphaerella irregulari |
|
|
| 249586 |
Mycosphaerella marksii AY725556 |
112484
|
3234158
|
| 249613 |
Mycosphaerella marksii CPC 14655 |
112484
|
3234158
|
| 249610 |
Mycosphaerella vietnamensis |
389362
|
10314178
|
| 249585 |
Passalora intermedia A11 |
|
|
| 249587 |
Passalora intermedia A12 |
|
|
| 249590 |
Passalora intermedia A13 |
|
|
| 249582 |
Passalora intermedia A17 |
|
|
| 249575 |
Passalora intermedia A21 |
|
|
| 249573 |
Passalora intermedia A23 |
|
|
| 249572 |
Passalora intermedia A24 |
|
|
| 249615 |
Passalora intermedia A25 |
|
|
| 249608 |
Passalora intermedia A26 |
|
|
| 249571 |
Passalora intermedia A27 |
|
|
| 249601 |
Passalora intermedia A30 |
|
|
| 249583 |
Passalora intermedia A31 |
|
|
| 249607 |
Passalora intermedia A32 |
|
|
| 249570 |
Passalora intermedia A33 |
|
|
| 249581 |
Passalora intermedia A36 |
|
|
| 249577 |
Passalora intermedia A37 |
|
|
| 249596 |
Passalora intermedia A39 |
|
|
| 249580 |
Pseudocercospora madagascariensis |
|
|
| 242670 |
Pseudocercospora paraguayensis |
131336
|
5962571
|
| 249593 |
Readeriella gauchensis |
|
|
| 249602 |
Readeriella zuluensis |
|
|
| 249603 |
Teratosphaeria hortaea A10 |
|
|
| 249600 |
Teratosphaeria hortaea A14 |
|
|
| 249569 |
Teratosphaeria hortaea A15 |
|
|
| 249609 |
Teratosphaeria hortaea A16 |
|
|
| 249597 |
Teratosphaeria hortaea A20 |
|
|
| 249599 |
Teratosphaeria hortaea A22 |
|
|
| 249591 |
Teratosphaeria hortaea A3 |
|
|
| 249574 |
Teratosphaeria hortaea A34 |
|
|
| 249588 |
Teratosphaeria hortaea A4 |
|
|
| 249579 |
Teratosphaeria hortaea A5 |
|
|
| 249589 |
Teratosphaeria hortaea A6 |
|
|
| 249578 |
Teratosphaeria hortaea A7 |
|
|
| 249605 |
Teratosphaeria hortaea A8 |
|
|
| 249616 |
Teratosphaeria hortaea A9 |
|
|
| 240705 |
Teratosphaeria molleriana |
112493
|
3922422
|
| 249612 |
Toxicocladosporium chlamydosporum A1 |
|
|
| 249618 |
Toxicocladosporium chlamydosporum A2 |
|
|
| 249594 |
Toxicocladosporium irritans |
470064
|
|
| 249568 |
Toxicocladosporium rubrigenum A18 |
|
|
| 249595 |
Toxicocladosporium rubrigenum A19 |
|
|
| 249614 |
Toxicocladosporium rubrigenum A28 |
|
|
| 249619 |
Toxicocladosporium veloxum |
|
|