@ARTICLE{TreeBASE2Ref23898,
author = {Karen Hansen and Ibai Olariaga},
title = {Species limits and relationships within Otidea inferred from multiple gene phylogenies},
year = {2015},
keywords = {distribution ectomycorrhizal associations gene conflict genealogical concordance mapping morphological features Pezizomycetes Pyronemataceae species recognition},
doi = {10.3767/003158515X687993},
url = {http://},
pmid = {},
journal = {Persoonia: Molecular Phylogeny and Evolution of Fungi},
volume = {35},
number = {},
pages = {148--165},
abstract = {The genus Otidea is one of the more conspicuous members of the Pyronemataceae, with high species
diversity in hemiboreal and boreal forests. The genus is morphologically coherent and in previous higher-level multigene
analyses it formed a highly supported monophyletic group. Species delimitation within Otidea is controversial
and much confusion has prevailed in the naming of taxa. To provide a phylogenetic hypothesis of Otidea, elucidate
species diversity and limits we compiled a four-gene dataset including the nuclear LSU rDNA and three nuclear
protein-coding genes (RPB1, RPB2 and EF-1?) for 89 specimens (total 4 877 nucleotides). These were selected from
a larger sample of material studied using morphology and 146 ITS (ITS1-5.8S-ITS2) and 168 LSU rDNA sequences
to represent the full genetic diversity. Using genealogical concordance phylogenetic species recognition (GCPSR),
Bayesian and maximum likelihood analyses of the individual datasets resolved 25 species of Otidea. An additional
eight singletons are considered to be distinct species, because they were genetically divergent from their sisters.
Sequences of multiple genes were included from 13 holotypes, one neotype and three epitypes. Otidea angusta,
O. myosotis and O. papillata f. pallidefurfuracea are nested within O. nannfeldtii, O. leporina and O. tuomikoskii,
respectively and are considered synonyms. Otidea cantharella var. minor is shown to be a distinct species. Five
new species were discovered: O. oregonensis and O. pseudoleporina for North America; and O. borealis, O. brunneoparva
and O. subformicarum for Europe. The analyses of the individual four gene datasets yielded phylogenies
that were highly concordant topologically, except for the RPB1 that showed supported conflict for some nodes in
Bayesian analysis. Excluding the RPB1 from the combined analyses produced an identical topology to the four-gene
phylogeny, but with higher support for several basal nodes and lower support for several shallow nodes. We argue
to use the three-gene dataset to retrieve the maximum support for the higher-level relationships in Otidea, but still
utilise the signal from the RPB1 for the delimitation and relationships of closely related species. From the four gene
regions utilised, EF-1? and RPB1 have the strongest species recognition power, and with higher amplification success
EF-1? may serve as the best secondary barcoding locus for Otidea (with ITS being a primary). The phylogeny
from the three- and four-gene datasets is fully resolved and strongly supported in all branches but one. Two major
clades, as part of six inclusive clades A?F, are identified ? and ten subclades within these: A) O. platyspora and
O. alutacea subclades, and B) O. papillata, O. leporina, O. tuomikoskii, O. cantharella, O. formicarum, O. unicisa,
O. bufonia-onotica and O. concinna subclades. Morphological features in Otidea appear to be fast evolving and
prone to shifts, and are poor indicators of higher-level relationships. Nevertheless, a conspicuous spore ornament is
a synapomorphy for the O. unicisa subclade (/Otideopsis); all other species in Otidea have smooth or verruculose (in
SEM) spores. Exclusively pale to bright yellow apothecia and straight to curved, broadly clavate to distinctly capitate
paraphyses are synapomorphies for a restricted O. concinna subclade (/Flavoscypha). The curved to hooked apices
of the paraphyses is suggested to be a symplesiomorphic trait for the genus. The reaction of resinous exudates
on the outermost excipular cells that coalesce into amber drops in Melzer?s reagent is likely an ancestral state for
clade B. We estimate that Otidea consists of 47 species worldwide, based on all available information (including
morphology, ITS or LSU sequences, and literature descriptions). Three fifths of the species occur in Europe, with
20 species recognised as endemic. At least 14 species occur in North America and 17 in Asia, with eight and ten
species considered endemic to each continent, respectively. Our knowledge about Otidea in Asia is still fragmentary
and the diversity likely much higher.}
}
Taxa for matrix 25001 of Study 16681

Citation title:
"Species limits and relationships within Otidea inferred from multiple gene phylogenies".

Study name:
"Species limits and relationships within Otidea inferred from multiple gene phylogenies".

This study is part of submission 16681
(Status: Published).
Taxa
Return to matrix row view
| ID |
Taxon Label |
NCBI taxid |
uBIO namebankID |
| 1662942 |
Monascella botryosa |
89420
|
3042666
|
| 1663003 |
Otidea aff subformicarum FH301035 |
|
|
| 1663009 |
Otidea aff subformicarum FH301036 |
|
|
| 1662993 |
Otidea alutacea ARAN_A3023204 |
88576
|
3034276
|
| 1662936 |
Otidea alutacea JS0881 |
88576
|
3034276
|
| 1662970 |
Otidea alutacea KH09133 |
88576
|
3034276
|
| 1662980 |
Otidea alutacea KH09135 |
88576
|
3034276
|
| 1662953 |
Otidea alutacea KH09170 |
88576
|
3034276
|
| 1662964 |
Otidea alutacea KH09178 |
88576
|
3034276
|
| 1662948 |
Otidea alutacea KH10193 |
88576
|
3034276
|
| 1663002 |
Otidea alutacea MC201005 |
88576
|
3034276
|
| 1662938 |
Otidea alutacea Moorefun19 |
88576
|
3034276
|
| 1662971 |
Otidea alutacea OSC56747 |
88576
|
3034276
|
| 1663023 |
Otidea alutacea OSC56758 |
88576
|
3034276
|
| 1662967 |
Otidea angusta Holotype |
|
|
| 1662954 |
Otidea apophysata NV136 |
566113
|
3069597
|
| 1662977 |
Otidea borealis S F_242694 |
|
|
| 1662974 |
Otidea brunneoparva KH08107 |
|
|
| 1663004 |
Otidea brunneoparva KH0982 |
|
|
| 1662947 |
Otidea brunneoparva TUR_A198579 |
|
|
| 1662988 |
Otidea bufonia KH0737 |
566114
|
3263004
|
| 1663008 |
Otidea bufonia KH09172 |
566114
|
3263004
|
| 1663022 |
Otidea bufonia KH09248 |
566114
|
3263004
|
| 1662992 |
Otidea bufonia KH09249 |
566114
|
3263004
|
| 1662972 |
Otidea bufonia NV20091101 |
566114
|
3263004
|
| 1662963 |
Otidea caeruleopruinosa Holotype |
|
|
| 1662973 |
Otidea caeruleopruinosa NV143 |
|
|
| 1663007 |
Otidea cantharella KH09125 |
566115
|
3083051
|
| 1662996 |
Otidea cantharella NV20080916 |
566115
|
3083051
|
| 1662943 |
Otidea concinna KH09183 |
88578
|
3083122
|
| 1662969 |
Otidea concinna KH09250 |
88578
|
3083122
|
| 1663010 |
Otidea daliensis SEST06081702 |
378508
|
3040251
|
| 1662937 |
Otidea flavidobrunneola H601083O |
|
|
| 1662965 |
Otidea flavidobrunneola Holotype |
|
|
| 1663011 |
Otidea flavidobrunneola KH09153 |
|
|
| 1662982 |
Otidea formicarum Holotype |
|
3198039
|
| 1662987 |
Otidea formicarum JS0863 |
|
3198039
|
| 1663016 |
Otidea formicarum S_F244372 |
|
3198039
|
| 1662979 |
Otidea leporina KH0993 |
47199
|
3072733
|
| 1662940 |
Otidea leporina NV20080928 |
47199
|
3072733
|
| 1663021 |
Otidea leporina OSC56784 |
47199
|
3072733
|
| 1663000 |
Otidea leporina OSC56824 |
47199
|
3072733
|
| 1662958 |
Otidea minor CL95091401 |
|
|
| 1662978 |
Otidea minor H6008618 |
|
|
| 1662959 |
Otidea minor KH10311 |
|
|
| 1662960 |
Otidea minor KH9884 |
|
|
| 1662999 |
Otidea mirabilis KH0109 |
|
3368790
|
| 1662989 |
Otidea mirabilis KH09188 |
|
3368790
|
| 1663015 |
Otidea mirabilis KH10285 |
|
3368790
|
| 1662983 |
Otidea mirabilis NV20080914 |
|
3368790
|
| 1662945 |
Otidea myosotis Holotype |
|
3198041
|
| 1662986 |
Otidea nannfeldtii Holotype |
|
3198042
|
| 1663017 |
Otidea nannfeldtii JS08103 |
|
3198042
|
| 1662994 |
Otidea nannfeldtii KH10302 |
|
3198042
|
| 1663006 |
Otidea nannfeldtii NV20081001 |
|
3198042
|
| 1662939 |
Otidea nannfeldtii Rh101310 |
|
3198042
|
| 1662949 |
Otidea nannfeldtii S_F249387 exH6017194 |
|
3198042
|
| 1663013 |
Otidea onotica C_F_89691 |
61494
|
3082369
|
| 1662957 |
Otidea onotica KH09136 |
61494
|
3082369
|
| 1662976 |
Otidea onotica KH10284 |
61494
|
3082369
|
| 1662995 |
Otidea onotica OSC56759 |
61494
|
3082369
|
| 1662998 |
Otidea oregonensis Moorefun31 |
|
|
| 1662956 |
Otidea oregonensis Moorefun58 |
|
|
| 1662962 |
Otidea oregonensis OSC56745 |
|
|
| 1662985 |
Otidea papillata Holotype |
|
3198043
|
| 1662951 |
Otidea papillata TUR102134 |
|
3198043
|
| 1662935 |
Otidea papillata f pallidefurfuracea NV20070927_Isotype |
|
|
| 1662944 |
Otidea phlebophora JV06385 |
566117
|
3082289
|
| 1662991 |
Otidea platyspora JV06656 |
566118
|
3213016
|
| 1662981 |
Otidea platyspora KH09163 |
566118
|
3213016
|
| 1663018 |
Otidea propinquata KH0999 |
|
3198044
|
| 1663001 |
Otidea propinquata NV20080915 |
|
3198044
|
| 1663019 |
Otidea pseudoleporina Moorefun14 |
|
|
| 1663020 |
Otidea pseudoleporina OSC56760 |
|
|
| 1662968 |
Otidea pseudoleporina OSC56809 |
|
|
| 1662966 |
Otidea pseudoleporina Rh10910 |
|
|
| 1662941 |
Otidea rainierensis Holotype |
88581
|
3183131
|
| 1662950 |
Otidea smithii Ecv3345 |
88582
|
3163782
|
| 1663005 |
Otidea smithii OSC56799 |
88582
|
3163782
|
| 1662990 |
Otidea sp B KH0979 |
|
|
| 1662952 |
Otidea subformicarum CL05092830 |
|
|
| 1662984 |
Otidea subformicarum NV128 |
|
|
| 1662955 |
Otidea tuomikoskii Holotype |
88583
|
3198046
|
| 1663014 |
Otidea tuomikoskii KH09130 |
88583
|
3198046
|
| 1662975 |
Otidea tuomikoskii NV20080908 |
88583
|
3198046
|
| 1662997 |
Otidea tuomikoskii OSC56761 |
88583
|
3198046
|
| 1663012 |
Otidea unicisa KH0606 |
|
3042743
|
| 1662961 |
Otidea yunnanensis TL6236 |
|
|
| 1662946 |
Warcupia terrestris |
353053
|
3203917
|