@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.}
}
Citation for 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).
Citation
Hansen K., & Olariaga I. 2015. Species limits and relationships within Otidea inferred from multiple gene phylogenies. Persoonia: Molecular Phylogeny and Evolution of Fungi, 35: 148-165.
Authors
-
Hansen K.
(submitter)
+46 (0)8 5195 4248
-
Olariaga I.
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.
Keywords
distribution ectomycorrhizal associations gene conflict genealogical concordance mapping morphological features Pezizomycetes Pyronemataceae species recognition
External links
About this resource
- Canonical resource URI:
http://purl.org/phylo/treebase/phylows/study/TB2:S16681
- Other versions:
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- Show BibTeX reference
@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.}
}
- Show RIS reference
TY - JOUR
ID - 23898
AU - Hansen,Karen
AU - Olariaga,Ibai
T1 - Species limits and relationships within Otidea inferred from multiple gene phylogenies
PY - 2015
KW - distribution ectomycorrhizal associations gene conflict genealogical concordance mapping morphological features Pezizomycetes Pyronemataceae species recognition
UR - http://dx.doi.org/10.3767/003158515X687993
N2 - 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.
L3 - 10.3767/003158515X687993
JF - Persoonia: Molecular Phylogeny and Evolution of Fungi
VL - 35
IS -
SP - 148
EP - 165
ER -