@ARTICLE{TreeBASE2Ref16482,
author = {H. Thorsten Lumbsch and Imke Schmitt and Maria Ines Messuti},
title = {Utility of nuclear SSU and LSU rDNA data sets to discover the ordinal placement of the Coccotremataceae (Ascomycota)},
year = {2001},
keywords = {ascomata; Ascomycota; Coccotremataceae; lichens; LSU rDNA; SSU rDNA},
doi = {10.1078/1439-6092-00008},
url = {},
pmid = {},
journal = {Organisms Diversity and Evolution},
volume = {1},
number = {2},
pages = {99--112},
abstract = {Informal ascomycete classifications have traditionally been based in part on ascomatal morphologies. The problems associated with grouping taxa using ascomatal characters are evidenced in the Coccotremataceae where the ascomata have been interpreted either as apothecia or perithecia. We used SSU rDNA sequences representing all classes of the Pezizomycotina to infer the phylogenetic position of the family. The Coccotremataceae clustered within the Lecanoromycetes. Since the Lecanoromycetes are characterized by the presence of apothecia, these data support the apothecial interpretation, given that the ascomata of the Coccotremataceae are not the result of convergent evolution. To evaluate the ordinal placement of the Coccotremataceae we used sequences of the SSU rRNA and LSU rRNA gene of 12 Lecanoromycetes. The SSU and LSU portions of this second analysis reveal conflicting phylogenies. Therefore we compared the two portions with additional statistical tests: splits decomposition, an analysis of the distribution of homoplasy, and a calculation of the ideal nucleotide substitution rate. In all of these tests the LSU data performed better than the SSU data. The results of the incongruence length difference (ILD) test suggest the data portions could be combined. There is no difference in the tree topology of the combined data set and of the LSU portion only, but the bootstrap values in the combined tree are lower. We argue that the low bootstrap supports in the combined tree are due to the phylogenetic signal in the SSU data set. Therefore we use the LSU and the combined tree to base our classification of the Coccotremataceae. In the LSU and the combined tree the inclusion of the Coccotremataceae in the Pertusariales is supported as is the sister relationship of the Pertusariales and Agyriales. Within the Pertusariales the Coccotremataceae and Pertusariaceae are well-supported sister taxa.}
}
Taxa for matrix 34253 of Study 719

Citation title:
"Utility of nuclear SSU and LSU rDNA data sets to discover the ordinal placement of the Coccotremataceae (Ascomycota)".

This study was previously identified under the legacy study ID S563
(Status: Published).
Taxa
Return to matrix row view
| ID |
Taxon Label |
NCBI taxid |
uBIO namebankID |
| 2063796 |
Polymastia andrica ZMBN98057 |
|
491348
|
| 2063846 |
Polymastia andrica ZMBN98074 |
|
491348
|
| 2063849 |
Polymastia arctica ZMBN98060 |
|
5477364
|
| 2063819 |
Polymastia arctica ZMBN98062 |
|
5477364
|
| 2063842 |
Polymastia arctica ZMBN98063 |
|
5477364
|
| 2063845 |
Polymastia arctica ZMBN98065 |
|
5477364
|
| 2063836 |
Polymastia arctica ZMBN98068 |
|
5477364
|
| 2063816 |
Polymastia bartletti ZMBN98111 |
|
7195140
|
| 2063803 |
Polymastia boletiformis ZMBN98047 |
|
2678729
|
| 2063823 |
Polymastia boletiformis ZMBN98089 |
|
2678729
|
| 2063824 |
Polymastia cf bartletti GNM904 1 |
|
|
| 2063801 |
Polymastia cf conigera BELUM MC3722 |
|
|
| 2063818 |
Polymastia corticata ZMBN98097 |
475993
|
9885317
|
| 2063831 |
Polymastia corticata ZMBN98104 |
475993
|
9885317
|
| 2063835 |
Polymastia corticata ZMBN98105 |
475993
|
9885317
|
| 2063815 |
Polymastia euplectella ZMBN98044 |
|
|
| 2063794 |
Polymastia grimaldii ZMBN98064 |
|
|
| 2063798 |
Polymastia invaginata ZMBN98046 |
283554
|
5979269
|
| 2063834 |
Polymastia invaginata ZMBN98093 |
283554
|
5979269
|
| 2063821 |
Polymastia invaginata ZMBN98094 |
283554
|
5979269
|
| 2063813 |
Polymastia mamillaris ZMBN98078 |
|
2678499
|
| 2063839 |
Polymastia mamillaris ZMBN98083 |
|
2678499
|
| 2063808 |
Polymastia penicillus BELUM MC6505 |
|
|
| 2063802 |
Polymastia sp1 ZMBN98091 |
|
|
| 2063827 |
Polymastia sp2 ZMBN98080 |
|
|
| 2063812 |
Polymastia thielei ZMBN98052 |
|
|
| 2063814 |
Polymastia uberrima ZMBN98066 |
|
|
| 2063832 |
Polymastia uberrima ZMBN98073 |
|
|
| 2063800 |
Quasillina brevis ZMBN98049 |
|
7195177
|
| 2063817 |
Radiella cf sarsi ZMBN98103 |
|
|
| 2063825 |
Radiella hemisphaerica ZMBN98043 |
|
|
| 2063820 |
Radiella hemisphaerica ZMBN98056 |
|
|
| 2063797 |
Radiella sarsi ZMBN98039 |
|
7205494
|
| 2063837 |
Radiella sp ZMBN98038 |
|
|
| 2063795 |
Sphaerotylus antarcticus ZMBN98045 |
|
5469693
|
| 2063809 |
Sphaerotylus borealis ZMBN98059 |
|
7195186
|
| 2063806 |
Sphaerotylus capitatus ZMBN98042 |
|
|
| 2063841 |
Sphaerotylus capitatus ZMBN98075 |
|
|
| 2063833 |
Sphaerotylus sp1 BELUM MC4236 |
|
|
| 2063811 |
Sphaerotylus sp2 BELUM MC5015 |
|
|
| 2063848 |
Spinularia spinularia ZMBN98037 |
283553
|
5979268
|
| 2063844 |
Spinularia spinularia ZMBN98079 |
283553
|
5979268
|
| 2063826 |
Suberites ficus BELUM MC4322 |
|
|
| 2063830 |
Tentorium papillatum SMF10571 |
|
6853444
|
| 2063822 |
Tentorium papillatum ZMBN98096 |
|
6853444
|
| 2063810 |
Tentorium semisuberites ZMBN98054 |
|
491338
|
| 2063805 |
Tentorium semisuberites ZMBN98099 |
|
491338
|
| 2063799 |
Tethya citrina BELUM MC5113 |
|
|
| 2063829 |
Weberella bursa ZMBN98051 |
|
7195204
|