@INCOLLECTION{TreeBASE2Ref22468,
author = {Christian H. Uhink and Joachim W. Kadereit},
title = {Phylogeny and Biogeography of the Hyoscyameae (Solanaceae): European - East Asian Disjunctions and the Origin of European Mountain Plant Taxa.},
year = {2009},
keywords = {ITS, ndhF/trnLF, BEAST, Bayesian relaxed molecular clock.},
doi = {},
url = {http://ubm.opus.hbz-nrw.de/volltexte/2009/2046/pdf/diss.pdf},
pmid = {},
booktitle = {Uhink C.H., eds. Biogeographische Beziehungen zwischen den Alpen, dem Kaukasus und den asiatischen Hochgebirgen.},
isbn = {},
publisher = {Johannes Gutenberg-Universit?t Mainz},
address = {Mainz},
editor = {Christian Helmut Uhink},
pages = {22--54},
abstract = {It has long been claimed that Asian high mountain areas constitute an important source for European mountain floras. The connection between these areas might have been through intervening mountain regions such as the Himalayas, Hindu Kush, Elburs and Caucasus, or along a more northern route. To address this question, we have analysed plant groups with a disjunct distribution in Eurasia (Europe, Caucasus and East Asia). Their phylogeny is expected to reveal the sequence of range splits in Eurasia, and to answer the question whether the European representatives are closely related to taxa in the Caucasus than to eastern representatives or not. If yes, this is interpreted as evidence in favour of a mountain route from Asia into Europe. The Hyoscyameae, a tribe of Solanaceae, consisting of Atropa, Scopolia, Hyoscyamus, Physochlaina, Atropanthe, Anisodus and Prezewalskia is a well-supported monophyletic clade. Whereas the latter three genera have a rather narrow distribution area and are endemic to W China and the Himalayas, the remaining genera are widely or disjunctly distributed in Asia and reach into Europe and even N Africa. Several taxa of Hyoscyameae have a montane or alpine ecology and are associated with mountain ranges. We reconstructed the phylogeny of the Hyoscyameae using nuclear and plastid markers. All genera were found to be monophyletic, but relationships among them are not fully supported. In the Prezewalskia/Physochlaina/Scopolia clade first branches are mainly found 21
in W China and C Asia and the close relationship between European/Caucasian and Japanese Scopolia taxa supports the assumption of a northern connection between the European mountains and E Asia. This is congruent with results obtained by us in Epimedium (Berberidaceae). In Atropa, A. baetica from N Africa/Southwest Europe is sister to the remainder of the genus which is distributed across Europe, in the Caucasus and in C Asia. The Himalayan A. acuminatum can not be distinguished from the European A. belladonna on the DNA-sequence level, and both are part of a polytomy together with Caucasian and C Asian taxa. Although these latter results do not allow us to draw any conclusions about the relationships and possible origin of most of the European material of Atropa, the sister group relationship of A. baetica to the rest of the genus may imply that much in contrast to our findings in the Prezewalskia/Physochlaina/Scopolia-clade, range formation in Atropa proceeded from west to east.}
}
Taxa for matrix 4624 of Study 10940

Citation title:
"Phylogeny and Biogeography of the Hyoscyameae (Solanaceae): European - East Asian Disjunctions and the Origin of European Mountain Plant Taxa.".

Study name:
"Phylogeny and Biogeography of the Hyoscyameae (Solanaceae): European - East Asian Disjunctions and the Origin of European Mountain Plant Taxa.".

This study is part of submission 10930
(Status: Published).
Taxa
Return to matrix row view
ID |
Taxon Label |
NCBI taxid |
uBIO namebankID |
256074 |
Ceratocystiopsis collifera CBS126.89 |
5160
|
3041026
|
256066 |
Ceratocystis deltoideospora WIN.M.41 |
0
|
3190499
|
264517 |
Grosmannia aurea CBS438.69 |
95157
|
10162085
|
256070 |
Grosmannia cucullata C1216 |
67628
|
10150730
|
264501 |
Grosmannia davidsonii WIN.M.1132 |
96396
|
10162725
|
256065 |
Grosmannia davidsonii WIN.M.1494 |
96396
|
10162725
|
256068 |
Grosmannia davidsonii WIN.M.1495 |
96396
|
10162725
|
256098 |
Grosmannia davidsonii WIN.M.60B |
96396
|
10162725
|
256071 |
Grosmannia dryocoetis CBS376.66 |
95154
|
10162082
|
256084 |
Grosmannia europhioides CBS229.83 |
67631
|
10150731
|
256067 |
Grosmannia europhioides MUCL18355 |
67631
|
10150731
|
256082 |
Grosmannia europhioides NFRI80.67.22 |
67631
|
10150731
|
256101 |
Grosmannia francke grosmanniae ATCC22061 |
|
|
256080 |
Grosmannia galeiformis C1101 |
255215
|
10237245
|
264504 |
Grosmannia galeiformis CECT20482 |
255215
|
10237245
|
256087 |
Grosmannia huntii WIN.M.492 |
155651
|
10190557
|
256090 |
Grosmannia laricis CBS636.94 |
150547
|
9815817
|
256075 |
Grosmannia penicillata NFRI60.21 |
360150
|
3147743
|
256073 |
Grosmannia penicillata WIN.M.131 |
360150
|
3147743
|
256060 |
Grosmannia piceaperda WIN.M.1380 |
96400
|
3147819
|
256058 |
Grosmannia piceaperda WIN.M.980 |
96400
|
3147819
|
256085 |
Grosmannia pseudoeurophioides WIN.M.42 |
96401
|
10162730
|
256081 |
Grosmannia wageneri ATCC58579 |
360468
|
10295291
|
256089 |
Hyalopesotum pini WIN.M.82.89 |
0
|
3048519
|
256093 |
Leptographium americanum WIN.M.1456 |
336015
|
3279779
|
264508 |
Leptographium lundbergii CBS352.29 |
96373
|
3158333
|
256083 |
Leptographium lundbergii DAOM64746 |
96373
|
3158333
|
256100 |
Leptographium lundbergii DSMZ5010 |
96373
|
3158333
|
256072 |
Leptographium lundbergii NFRI60.25 |
96373
|
3158333
|
256091 |
Leptographium lundbergii NFRI69.148 |
96373
|
3158333
|
256061 |
Leptographium lundbergii NFRI89.1040.1.3 |
96373
|
3158333
|
264518 |
Leptographium procerum DAOM33940 |
100367
|
3022655
|
256062 |
Leptographium procerum NFRI59.84.2 |
100367
|
3022655
|
264495 |
Leptographium procerum TOM73.12 |
100367
|
3022655
|
264519 |
Leptographium procerum TOM76.8 |
100367
|
3022655
|
264499 |
Leptographium procerum WIN.M.1264 |
100367
|
3022655
|
256103 |
Leptographium sp J.R.88.194A |
|
|
264503 |
Leptographium sp WIN.M.1106 |
|
|
264497 |
Leptographium sp WIN.M.1247 |
|
|
256088 |
Leptographium sp WIN.M.1269 |
|
|
256063 |
Leptographium sp WIN.M.528 |
|
|
256095 |
Leptographium sp WIN.M.984 |
|
|
256078 |
Leptographium sp WIN.M.985 |
|
|
264500 |
Leptographium terebrantis CBS298.85 |
96390
|
3195935
|
264511 |
Leptographium terebrantis CBS337.70 |
96390
|
3195935
|
264496 |
Leptographium terebrantis CBS408.61 |
96390
|
3195935
|
256079 |
Leptographium terebrantis UAMH9690 |
96390
|
3195935
|
256086 |
Leptographium terebrantis UAMH9722 |
96390
|
3195935
|
264512 |
Leptographium truncatum CBS929.85 |
330483
|
3022657
|
256077 |
Leptographium truncatum NFRI1813.1 |
330483
|
3022657
|
264509 |
Leptographium truncatum TOM74.29 |
330483
|
3022657
|
264513 |
Leptographium truncatum TOM86.30 |
330483
|
3022657
|
264510 |
Leptographium wingfieldii CBS645.89 |
155675
|
3039765
|
256076 |
Leptographium wingfieldii CBS648.89 |
155675
|
3039765
|
264516 |
Leptographium wingfieldii MCC125 |
155675
|
3039765
|
264515 |
Leptographium wingfieldii MCC130 |
155675
|
3039765
|
264498 |
Leptographium wingfieldii MCC349 |
155675
|
3039765
|
264505 |
Leptographium wingfieldii TOM10.2 |
155675
|
3039765
|
256096 |
Leptographium wingfieldii TOM11.5 |
155675
|
3039765
|
256059 |
Leptographium wingfieldii TOM59.21 |
155675
|
3039765
|
256069 |
Leptographium wingfieldii WIN.M.1218 |
155675
|
3039765
|
256064 |
Leptographium wingfieldii WIN.M.1322 |
155675
|
3039765
|
264507 |
Leptographium wingfieldii WIN.M.1382 |
155675
|
3039765
|
256094 |
Leptographium wingfieldii WIN.M.1482 |
155675
|
3039765
|
256102 |
Ophiostoma brevicolle CBS159.78 |
96393
|
3024063
|
256097 |
Pesotum sp WIN.M.1423 |
|
|
264506 |
Pesotum sp WIN.M.1428 |
|
|
264502 |
Pesotum sp WIN.M.478 |
|
|
256092 |
Pesotum sp WIN.M.481 |
|
|
264514 |
taxon 70 |
|
|