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<document ID-DOI="http://dx.doi.org/10.3897/mycokeys.74.57824" ID-GBIF-Dataset="4b352ef7-f73e-486b-948c-c37e0ab684a9" ID-PMC="PMC7588497" ID-Pensoft-Pub="1314-4049-74-17" ID-Pensoft-UUID="ABBEDA6BFAD45DC6BC542EFF61A9C78F" ID-PubMed="33149721" ModsDocID="1314-4049-74-17" checkinTime="1603157220132" checkinUser="pensoft" docAuthor="Reblova, Martina, Nekvindova, Jana, Fournier, Jacques &amp; Miller, Andrew N." docDate="2020" docId="62B7969B14E25D0397B072912621B66F" docLanguage="en" docName="MycoKeys 74: 17-74" docOrigin="MycoKeys 74" docSource="http://dx.doi.org/10.3897/mycokeys.74.57824" docTitle="Paragaeumannomyces sabinianus Réblová &amp; Nekvindová &amp; Fournier &amp; Miller 2020, sp. nov." docType="treatment" docVersion="4" id="ABBEDA6BFAD45DC6BC542EFF61A9C78F" lastPageNumber="17" masterDocId="ABBEDA6BFAD45DC6BC542EFF61A9C78F" masterDocTitle="Delimitation, new species and teleomorph-anamorph relationships in Codinaea, Dendrophoma, Paragaeumannomyces and Striatosphaeria (Chaetosphaeriaceae)" masterLastPageNumber="74" masterPageNumber="17" pageNumber="17" updateTime="1668136560939" updateUser="ExternalLinkService">
<mods:mods xmlns:mods="http://www.loc.gov/mods/v3">
<mods:titleInfo>
<mods:title>Delimitation, new species and teleomorph-anamorph relationships in Codinaea, Dendrophoma, Paragaeumannomyces and Striatosphaeria (Chaetosphaeriaceae)</mods:title>
</mods:titleInfo>
<mods:name type="personal">
<mods:role>
<mods:roleTerm>Author</mods:roleTerm>
</mods:role>
<mods:namePart>Reblova, Martina</mods:namePart>
<mods:affiliation>The Czech Academy of Sciences, Institute of Botany, Department of Taxonomy, Pruhonice 252 43, Czech Republic</mods:affiliation>
<mods:nameIdentifier type="orcid">https://orcid.org/0000-0001-5229-1709</mods:nameIdentifier>
<mods:nameIdentifier type="email">martina.reblova@ibot.cas.cz</mods:nameIdentifier>
</mods:name>
<mods:name type="personal">
<mods:role>
<mods:roleTerm>Author</mods:roleTerm>
</mods:role>
<mods:namePart>Nekvindova, Jana</mods:namePart>
<mods:affiliation>Department of Clinical Biochemistry and Diagnostics, University Hospital Hradec Kralove, Hradec Kralove 500 05, Czech Republic</mods:affiliation>
<mods:nameIdentifier type="orcid">https://orcid.org/0000-0002-2861-5483</mods:nameIdentifier>
</mods:name>
<mods:name type="personal">
<mods:role>
<mods:roleTerm>Author</mods:roleTerm>
</mods:role>
<mods:namePart>Fournier, Jacques</mods:namePart>
<mods:affiliation>Las Muros, Rimont 09420, France</mods:affiliation>
</mods:name>
<mods:name type="personal">
<mods:role>
<mods:roleTerm>Author</mods:roleTerm>
</mods:role>
<mods:namePart>Miller, Andrew N.</mods:namePart>
<mods:affiliation>Illinois Natural History Survey, University of Illinois Urbana-Champaign, Champaign, Illinois 61820, USA</mods:affiliation>
<mods:nameIdentifier type="orcid">https://orcid.org/0000-0001-7300-0069</mods:nameIdentifier>
</mods:name>
<mods:typeOfResource>text</mods:typeOfResource>
<mods:relatedItem type="host">
<mods:titleInfo>
<mods:title>MycoKeys</mods:title>
</mods:titleInfo>
<mods:part>
<mods:date>2020</mods:date>
<mods:detail type="volume">
<mods:number>74</mods:number>
</mods:detail>
<mods:extent unit="page">
<mods:start>17</mods:start>
<mods:end>74</mods:end>
</mods:extent>
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<mods:location>
<mods:url>http://dx.doi.org/10.3897/mycokeys.74.57824</mods:url>
</mods:location>
<mods:classification>journal article</mods:classification>
<mods:identifier type="DOI">http://dx.doi.org/10.3897/mycokeys.74.57824</mods:identifier>
<mods:identifier type="Pensoft-Pub">1314-4049-74-17</mods:identifier>
<mods:identifier type="Pensoft-UUID">ABBEDA6BFAD45DC6BC542EFF61A9C78F</mods:identifier>
</mods:mods>
<treatment ID-GBIF-Taxon="168501686" LSID="urn:lsid:plazi:treatment:62B7969B14E25D0397B072912621B66F" httpUri="http://treatment.plazi.org/id/62B7969B14E25D0397B072912621B66F" lastPageNumber="17" pageId="0" pageNumber="17">
<subSubSection pageId="0" pageNumber="17" type="nomenclature">
<paragraph pageId="0" pageNumber="17">
<taxonomicName LSID="62B7969B-14E2-5D03-97B0-72912621B66F" authority="Réblová &amp; A. N. Mill." authorityName="Réblová &amp; Nekvindová &amp; Fournier &amp; Miller" authorityYear="2020" class="Sordariomycetes" family="Chaetosphaeriaceae" genus="Paragaeumannomyces" higherTaxonomySource="CoL" kingdom="Fungi" lsidName="Paragaeumannomyces sabinianus" order="Chaetosphaeriales" pageId="0" pageNumber="17" phylum="Ascomycota" rank="species" species="sabinianus" status="sp. nov.">
Paragaeumannomyces sabinianus
<normalizedToken originalValue="Réblová">Reblova</normalizedToken>
&amp; A.N. Mill.
</taxonomicName>
<taxonomicNameLabel pageId="0" pageNumber="17">sp. nov.</taxonomicNameLabel>
<figureCitation captionStart="Figure 9" captionStartId="F9" captionText="Figure 9. Paragaeumannomyces sabinianus. A ascomata. B ascomatal setae C vertical section of ascomal wall D, E ascomal wall F, G upper part of the ascoma with ostiole surrounded by setae H setae from the ostiolar region I paraphyses J ascal apex with apical ring K asci L, M ascospores. Images: ILLS 00121384 (A, B, D, E, G-K); S. M. H. 3824 (C, F, L); S. M. H. 3807 (M). Scale bars: 500 μm (A); 20 μm (B, E, G, H); 100 μm (C, D); 25 μm (F); 5 μm (J); 10 μm (I, K-M)." figureDoi="10.3897/mycokeys.74.57824.figure9" httpUri="https://binary.pensoft.net/fig/464290" pageId="0" pageNumber="17">Figure 9</figureCitation>
</paragraph>
</subSubSection>
<subSubSection pageId="0" pageNumber="17" type="typification">
<paragraph pageId="0" pageNumber="17">Typification.</paragraph>
<paragraph pageId="0" pageNumber="17">
USA - Tennessee • Sevier Co., Great Smoky Mountains National Park, Twin Creeks, Twin Creeks Nature Trail, near ATBI plot; alt. 549 m; 11 Oct. 2006; on decaying wood; A.N. Miller &amp; P. Chaudhary leg.; A.N.M. 1011 (
<emphasis bold="true" pageId="0" pageNumber="17">holotype</emphasis>
: ILLS00121384!).
</paragraph>
</subSubSection>
<subSubSection pageId="0" pageNumber="17" type="etymology">
<paragraph pageId="0" pageNumber="17">Etymology.</paragraph>
<paragraph pageId="0" pageNumber="17">
The species epithet is proposed in honour of Sabine M. Huhndorf for her contribution to mycology and studies in
<taxonomicName authorityName="L.R.Tulasne &amp; C.Tulasne" authorityYear="1863" class="Sordariomycetes" family="Chaetosphaeriaceae" genus="Chaetosphaeria" higherTaxonomySource="CoL" kingdom="Fungi" lsidName="Chaetosphaeria" order="Chaetosphaeriales" pageId="0" pageNumber="17" phylum="Ascomycota" rank="genus">
<emphasis italics="true" pageId="0" pageNumber="17">Chaetosphaeria</emphasis>
</taxonomicName>
.
</paragraph>
</subSubSection>
<subSubSection pageId="0" pageNumber="17" type="description">
<paragraph pageId="0" pageNumber="17">Description on the natural substrate.</paragraph>
<paragraph pageId="0" pageNumber="17">
Teleomorph: Ascomata perithecial, non-stromatic, superficial, usually solitary or in small groups, 250-300(-400)
<normalizedToken originalValue="μm">μm</normalizedToken>
diam, 280-320
<normalizedToken originalValue="μm">μm</normalizedToken>
high, subglobose to broadly conical, rarely collapsing laterally upon drying, finely roughened, dark reddish-brown except for a black indistinct papilla, setose, setae 30-41.5
<normalizedToken originalValue="×">x</normalizedToken>
4-5
<normalizedToken originalValue="μm">μm</normalizedToken>
, dark brown, stiff, acute, scattered over entire ascoma, shorter and narrower setae 16.5-35
<normalizedToken originalValue="×">x</normalizedToken>
2.5-3
<normalizedToken originalValue="μm">μm</normalizedToken>
densely aggregated around the ostiole. Ostiole periphysate. Ascomatal wall leathery, three-layered. Outer layer of textura angularis, 32-53
<normalizedToken originalValue="μm">μm</normalizedToken>
thick, consisting of thin-walled, globose to subglobose, dark orange-brown to reddish-brown cells, 11.5-28
<normalizedToken originalValue="μm">μm</normalizedToken>
diam. Middle layer of textura prismatica, 12-22
<normalizedToken originalValue="μm">μm</normalizedToken>
thick, composed of thick-walled, polyhedral, dark brown, melanised cells. Inner layer of textura prismatica, 3-5
<normalizedToken originalValue="μm">μm</normalizedToken>
thick, composed of thin-walled, flattened and elongated hyaline to subhyaline cells. Paraphyses abundant, hyaline, sparsely branched, septate, 3.5-4.5(-6)
<normalizedToken originalValue="μm">μm</normalizedToken>
wide, tapering to 2-2.5
<normalizedToken originalValue="μm">μm</normalizedToken>
, longer than the asci. Asci (154-)161-189
<normalizedToken originalValue="×">x</normalizedToken>
(11-)12.5-14.5(-15.5)
<normalizedToken originalValue="μm">μm</normalizedToken>
(mean
<normalizedToken originalValue="±">+/-</normalizedToken>
SD = 174.2
<normalizedToken originalValue="±">+/-</normalizedToken>
8.7
<normalizedToken originalValue="×">x</normalizedToken>
13.0
<normalizedToken originalValue="±">+/-</normalizedToken>
0.8
<normalizedToken originalValue="μm">μm</normalizedToken>
), (130-)144-165
<normalizedToken originalValue="µm">µm</normalizedToken>
(mean
<normalizedToken originalValue="±">+/-</normalizedToken>
SD = 155.2
<normalizedToken originalValue="±">+/-</normalizedToken>
8.3
<normalizedToken originalValue="μm">μm</normalizedToken>
) long in the sporiferous part, cylindrical-fusiform, stipitate, apically broadly rounded to obtuse, ascal apex non-amyloid with a distinct apical annulus 2.5-3
<normalizedToken originalValue="μm">μm</normalizedToken>
wide, 1.5-2
<normalizedToken originalValue="μm">μm</normalizedToken>
high. Ascospores (64.5-)68.5-86.5(-88.5)
<normalizedToken originalValue="×">x</normalizedToken>
(3-)3.5-4.5
<normalizedToken originalValue="μm">μm</normalizedToken>
, (mean
<normalizedToken originalValue="±">+/-</normalizedToken>
SD = 79.1
<normalizedToken originalValue="±">+/-</normalizedToken>
5.3
<normalizedToken originalValue="×">x</normalizedToken>
4.0
<normalizedToken originalValue="±">+/-</normalizedToken>
0.3
<normalizedToken originalValue="μm">μm</normalizedToken>
), filiform to cylindrical, straight or slightly curved to sigmoid, hyaline, 7-septate, septa often unevenly distributed, not constricted at the septa, asymmetrical, broadly rounded at the apical end and tapering towards the narrowly rounded basal end, with one or two guttules in each cell, 2-3-seriate, rarely 4-seriate, partially overlapping, with a negative or weak dextrinoid reaction in
<normalizedToken originalValue="Melzers">Melzer's</normalizedToken>
reagent. Anamorph: Unknown.
</paragraph>
<caption doi="10.3897/mycokeys.74.57824.figure9" httpUri="https://binary.pensoft.net/fig/464290" pageId="0" pageNumber="17" start="Figure 9" startId="F9">
<paragraph pageId="0" pageNumber="17">
<emphasis bold="true" pageId="0" pageNumber="17">Figure 9.</emphasis>
<taxonomicName class="Sordariomycetes" family="Chaetosphaeriaceae" genus="Paragaeumannomyces" higherTaxonomySource="CoL" kingdom="Fungi" lsidName="Paragaeumannomyces sabinianus" order="Chaetosphaeriales" pageId="0" pageNumber="17" phylum="Ascomycota" rank="species" species="sabinianus">
<emphasis italics="true" pageId="0" pageNumber="17">Paragaeumannomyces sabinianus</emphasis>
</taxonomicName>
.
<emphasis bold="true" pageId="0" pageNumber="17">A</emphasis>
ascomata.
<emphasis bold="true" pageId="0" pageNumber="17">B</emphasis>
ascomatal setae
<emphasis bold="true" pageId="0" pageNumber="17">C</emphasis>
vertical section of ascomal wall
<emphasis bold="true" pageId="0" pageNumber="17">D, E</emphasis>
ascomal wall
<emphasis bold="true" pageId="0" pageNumber="17">F, G</emphasis>
upper part of the ascoma with ostiole surrounded by setae
<emphasis bold="true" pageId="0" pageNumber="17">H</emphasis>
setae from the ostiolar region
<emphasis bold="true" pageId="0" pageNumber="17">I</emphasis>
paraphyses
<emphasis bold="true" pageId="0" pageNumber="17">J</emphasis>
ascal apex with apical ring
<emphasis bold="true" pageId="0" pageNumber="17">K</emphasis>
asci
<emphasis bold="true" pageId="0" pageNumber="17">L, M</emphasis>
ascospores. Images: ILLS00121384 (
<emphasis bold="true" pageId="0" pageNumber="17">A, B, D, E, G-K</emphasis>
); S.M.H. 3824 (
<emphasis bold="true" pageId="0" pageNumber="17">C, F, L</emphasis>
); S.M.H. 3807 (
<emphasis bold="true" pageId="0" pageNumber="17">M</emphasis>
). Scale bars: 500
<normalizedToken originalValue="μm">μm</normalizedToken>
(
<emphasis bold="true" pageId="0" pageNumber="17">A</emphasis>
); 20
<normalizedToken originalValue="μm">μm</normalizedToken>
(
<emphasis bold="true" pageId="0" pageNumber="17">B, E, G, H</emphasis>
); 100
<normalizedToken originalValue="μm">μm</normalizedToken>
(
<emphasis bold="true" pageId="0" pageNumber="17">C, D</emphasis>
); 25
<normalizedToken originalValue="μm">μm</normalizedToken>
(
<emphasis bold="true" pageId="0" pageNumber="17">F</emphasis>
); 5
<normalizedToken originalValue="μm">μm</normalizedToken>
(
<emphasis bold="true" pageId="0" pageNumber="17">J</emphasis>
); 10
<normalizedToken originalValue="μm">μm</normalizedToken>
(
<emphasis bold="true" pageId="0" pageNumber="17">I, K-M</emphasis>
).
</paragraph>
</caption>
</subSubSection>
<subSubSection pageId="0" pageNumber="17" type="other specimen examined">
<paragraph pageId="0" pageNumber="17">Other specimen examined.</paragraph>
<paragraph pageId="0" pageNumber="17">
USA - North Carolina • Macon Co., Coweeta Hydrological Laboratory; 27 Jun. 1998, on decorticated wood; F.A.
<normalizedToken originalValue="Fernández">Fernandez</normalizedToken>
leg.; S.M.H. 3807. •
<emphasis italics="true" pageId="0" pageNumber="17">Ibid.</emphasis>
, Horse Cove Drive &amp; Bull Pen Road, alt. 1000 m; 27 Jun. 1998; on decorticated wood; F.A.
<normalizedToken originalValue="Fernández">Fernandez</normalizedToken>
leg.; S.M.H. 3824.
</paragraph>
</subSubSection>
<subSubSection pageId="0" pageNumber="17" type="habitat">
<paragraph pageId="0" pageNumber="17">Habitat and distribution.</paragraph>
<paragraph pageId="0" pageNumber="17">
A saprobe on decaying wood, so far known from North America in the USA (North Carolina, Tennessee) (Ellis 1887;
<bibRefCitation author="Huhndorf, SM" journalOrPublisher="Fungal Diversity" pageId="0" pageNumber="17" pagination="23 - 49" refId="B45" refString="Huhndorf, SM, Fernandez, FA, 2005. Teleomorph-anamorph connections: Chaetosphaeria raciborskii and related species, and their Craspedodidymum -like anamorphs. Fungal Diversity 19: 23 - 49" title="Teleomorph-anamorph connections: Chaetosphaeria raciborskii and related species, and their Craspedodidymum - like anamorphs." volume="19" year="2005">
Huhndorf and
<normalizedToken originalValue="Fernández">Fernandez</normalizedToken>
2005
</bibRefCitation>
).
</paragraph>
</subSubSection>
<subSubSection pageId="0" pageNumber="17" type="notes">
<paragraph pageId="0" pageNumber="17">Notes.</paragraph>
<paragraph pageId="0" pageNumber="17">
<bibRefCitation author="Huhndorf, SM" journalOrPublisher="Fungal Diversity" pageId="0" pageNumber="17" pagination="23 - 49" refId="B45" refString="Huhndorf, SM, Fernandez, FA, 2005. Teleomorph-anamorph connections: Chaetosphaeria raciborskii and related species, and their Craspedodidymum -like anamorphs. Fungal Diversity 19: 23 - 49" title="Teleomorph-anamorph connections: Chaetosphaeria raciborskii and related species, and their Craspedodidymum - like anamorphs." volume="19" year="2005">
Huhndorf and
<normalizedToken originalValue="Fernández">Fernandez</normalizedToken>
(2005)
</bibRefCitation>
reported
<taxonomicName lsidName="P. longisporus" pageId="0" pageNumber="17" rank="species" species="longisporus">
<emphasis italics="true" pageId="0" pageNumber="17">P. longisporus</emphasis>
</taxonomicName>
(as
<taxonomicName lsidName="Ch. ellisii" pageId="0" pageNumber="17" rank="species" species="ellisii">
<emphasis italics="true" pageId="0" pageNumber="17">Ch. ellisii</emphasis>
</taxonomicName>
) from numerous collections from North America; the phylogenetic analysis of ITS sequences of six specimens resolved this species as a statistically unsupported clade with two strongly supported subclades. Although
<bibRefCitation author="Huhndorf, SM" journalOrPublisher="Fungal Diversity" pageId="0" pageNumber="17" pagination="23 - 49" refId="B45" refString="Huhndorf, SM, Fernandez, FA, 2005. Teleomorph-anamorph connections: Chaetosphaeria raciborskii and related species, and their Craspedodidymum -like anamorphs. Fungal Diversity 19: 23 - 49" title="Teleomorph-anamorph connections: Chaetosphaeria raciborskii and related species, and their Craspedodidymum - like anamorphs." volume="19" year="2005">
Huhndorf and
<normalizedToken originalValue="Fernández">Fernandez</normalizedToken>
(2005)
</bibRefCitation>
described
<taxonomicName lsidName="P. longisporus" pageId="0" pageNumber="17" rank="species" species="longisporus">
<emphasis italics="true" pageId="0" pageNumber="17">P. longisporus</emphasis>
</taxonomicName>
with setae scattered over the entire ascoma, in discussion, they admitted the presence of setae also around the ostiole: &quot;In
<taxonomicName lsidName="C. ellisii" pageId="0" pageNumber="17" rank="species" species="ellisii">
<emphasis italics="true" pageId="0" pageNumber="17">C. ellisii</emphasis>
</taxonomicName>
,
<taxonomicName lsidName="C. raciborskii" pageId="0" pageNumber="17" rank="species" species="raciborskii">
<emphasis italics="true" pageId="0" pageNumber="17">C. raciborskii</emphasis>
</taxonomicName>
and
<taxonomicName lsidName="C. panamensis" pageId="0" pageNumber="17" rank="species" species="panamensis">
<emphasis italics="true" pageId="0" pageNumber="17">C. panamensis</emphasis>
</taxonomicName>
the setae tend to be scattered over the entire surface of the ascomata, however some specimens of
<taxonomicName lsidName="C. ellisii" pageId="0" pageNumber="17" rank="species" species="ellisii">
<emphasis italics="true" pageId="0" pageNumber="17">C. ellisii</emphasis>
</taxonomicName>
may have setae concentrated only at the apex.&quot;
</paragraph>
<paragraph pageId="0" pageNumber="17">
<bibRefCitation author="Barr, ME" journalOrPublisher="Mycotaxon" pageId="0" pageNumber="17" pagination="45 - 76" refId="B3" refString="Barr, ME, 1993. Redisposition of some taxa described by J.B. Ellis. Mycotaxon 46: 45 - 76" title="Redisposition of some taxa described by J. B. Ellis." volume="46" year="1993">Barr (1993)</bibRefCitation>
described the ostiole of the holotype of
<taxonomicName lsidName="S. longispora" pageId="0" pageNumber="17" rank="species" species="longispora">
<emphasis italics="true" pageId="0" pageNumber="17">S. longispora</emphasis>
</taxonomicName>
surrounded by a crown of dark brown, stiff setae. We examined three collections tentatively identified as
<taxonomicName lsidName="P. longisporus" pageId="0" pageNumber="17" rank="species" species="longisporus">
<emphasis italics="true" pageId="0" pageNumber="17">P. longisporus</emphasis>
</taxonomicName>
from North America (ILLS00121384, ILLS00121385, ILLS00121386) and in each the ostiole was delimited by densely aggregated acute setae. Apart from the ostiolar setae, additional setae were scattered over the entire ascoma, but they differed by their density among collections. The ascomata and asci of these three collections are comparable in size; the main difference lies in the ascospore length. The specimen ILLS00121384 has longer [(64.5-)68.5-86.5(-88.5)
<normalizedToken originalValue="μm">μm</normalizedToken>
] ascospores compared to ILLS00121385 and ILLS00121386, which have shorter [(50.5-)52.5-68
<normalizedToken originalValue="μm">μm</normalizedToken>
] ascospores corresponding to the size given by
<bibRefCitation author="Barr, ME" journalOrPublisher="Mycotaxon" pageId="0" pageNumber="17" pagination="45 - 76" refId="B3" refString="Barr, ME, 1993. Redisposition of some taxa described by J.B. Ellis. Mycotaxon 46: 45 - 76" title="Redisposition of some taxa described by J. B. Ellis." volume="46" year="1993">Barr (1993)</bibRefCitation>
for the
<taxonomicName lsidName="S. longispora" pageId="0" pageNumber="17" rank="species" species="longispora">
<emphasis italics="true" pageId="0" pageNumber="17">S. longispora</emphasis>
</taxonomicName>
holotype. In the description of
<taxonomicName lsidName="P. longisporus" pageId="0" pageNumber="17" rank="species" species="longisporus">
<emphasis italics="true" pageId="0" pageNumber="17">P. longisporus</emphasis>
</taxonomicName>
<emphasis italics="true" pageId="0" pageNumber="17">fide</emphasis>
<bibRefCitation author="Huhndorf, SM" journalOrPublisher="Fungal Diversity" pageId="0" pageNumber="17" pagination="23 - 49" refId="B45" refString="Huhndorf, SM, Fernandez, FA, 2005. Teleomorph-anamorph connections: Chaetosphaeria raciborskii and related species, and their Craspedodidymum -like anamorphs. Fungal Diversity 19: 23 - 49" title="Teleomorph-anamorph connections: Chaetosphaeria raciborskii and related species, and their Craspedodidymum - like anamorphs." volume="19" year="2005">
Huhndorf and
<normalizedToken originalValue="Fernández">Fernandez</normalizedToken>
(2005)
</bibRefCitation>
, a wide range of ascospore lengths [(40-)50-75(-80)
<normalizedToken originalValue="μm">μm</normalizedToken>
] is given, the upper limit matching the ascospore size of ILLS00121384.
</paragraph>
<paragraph pageId="0" pageNumber="17">
In our ITS-28S phylogeny,
<taxonomicName lsidName="P. longisporus" pageId="0" pageNumber="17" rank="species" species="longisporus">
<emphasis italics="true" pageId="0" pageNumber="17">P. longisporus</emphasis>
</taxonomicName>
<emphasis italics="true" pageId="0" pageNumber="17">fide</emphasis>
<bibRefCitation author="Huhndorf, SM" journalOrPublisher="Fungal Diversity" pageId="0" pageNumber="17" pagination="23 - 49" refId="B45" refString="Huhndorf, SM, Fernandez, FA, 2005. Teleomorph-anamorph connections: Chaetosphaeria raciborskii and related species, and their Craspedodidymum -like anamorphs. Fungal Diversity 19: 23 - 49" title="Teleomorph-anamorph connections: Chaetosphaeria raciborskii and related species, and their Craspedodidymum - like anamorphs." volume="19" year="2005">
Huhndorf and
<normalizedToken originalValue="Fernández">Fernandez</normalizedToken>
(2005)
</bibRefCitation>
was resolved as a strongly supported clade (100/1.0/100) with two subclades. The first subclade (100/1.0/100) was introduced as a new species
<taxonomicName lsidName="P. sabinianus" pageId="0" pageNumber="17" rank="species" species="sabinianus">
<emphasis italics="true" pageId="0" pageNumber="17">P. sabinianus</emphasis>
</taxonomicName>
, including ILLS00121384 (Fig.
<figureCitation captionStart="Figure 9" captionStartId="F9" captionText="Figure 9. Paragaeumannomyces sabinianus. A ascomata. B ascomatal setae C vertical section of ascomal wall D, E ascomal wall F, G upper part of the ascoma with ostiole surrounded by setae H setae from the ostiolar region I paraphyses J ascal apex with apical ring K asci L, M ascospores. Images: ILLS 00121384 (A, B, D, E, G-K); S. M. H. 3824 (C, F, L); S. M. H. 3807 (M). Scale bars: 500 μm (A); 20 μm (B, E, G, H); 100 μm (C, D); 25 μm (F); 5 μm (J); 10 μm (I, K-M)." figureDoi="10.3897/mycokeys.74.57824.figure9" httpUri="https://binary.pensoft.net/fig/464290" pageId="0" pageNumber="17">9</figureCitation>
), S.M.H. 3807 (
<bibRefCitation author="Huhndorf, SM" journalOrPublisher="Fungal Diversity" pageId="0" pageNumber="17" pagination="23 - 49" refId="B45" refString="Huhndorf, SM, Fernandez, FA, 2005. Teleomorph-anamorph connections: Chaetosphaeria raciborskii and related species, and their Craspedodidymum -like anamorphs. Fungal Diversity 19: 23 - 49" title="Teleomorph-anamorph connections: Chaetosphaeria raciborskii and related species, and their Craspedodidymum - like anamorphs." volume="19" year="2005">
Huhndorf and
<normalizedToken originalValue="Fernández">Fernandez</normalizedToken>
2005
</bibRefCitation>
: fig. 13) and S.M.H. 3824 (
<bibRefCitation author="Huhndorf, SM" journalOrPublisher="Fungal Diversity" pageId="0" pageNumber="17" pagination="23 - 49" refId="B45" refString="Huhndorf, SM, Fernandez, FA, 2005. Teleomorph-anamorph connections: Chaetosphaeria raciborskii and related species, and their Craspedodidymum -like anamorphs. Fungal Diversity 19: 23 - 49" title="Teleomorph-anamorph connections: Chaetosphaeria raciborskii and related species, and their Craspedodidymum - like anamorphs." volume="19" year="2005">
Huhndorf and
<normalizedToken originalValue="Fernández">Fernandez</normalizedToken>
2005
</bibRefCitation>
: fig. 15) with longer ascospores, distinguished from the second subclade
<taxonomicName lsidName="P. longisporus" pageId="0" pageNumber="17" rank="species" species="longisporus">
<emphasis italics="true" pageId="0" pageNumber="17">P. longisporus</emphasis>
</taxonomicName>
(99/1.0/100) with shorter ascospores (Fig.
<figureCitation captionStart="Figure 8" captionStartId="F8" captionText="Figure 8. Paragaeumannomyces longisporus. A, B ascomata C, D vertical section of ascomal wall E vertical section of ascomal wall and papilla with apical of setae F ascomal wall with setae G globose cells of the outer layer of the ascomal wall H, I asci J paraphyses K-N ascospores. Images: ILLS 00121385 (A, B, G); S. M. H. 3860 (C, E, M); S. M. H. 2519 (D); ILLS 00121386 (F, H-J, K); S. M. H. 2758 (L); S. M. H. 3809 (N). Scale bars: 250 μm (A-D); 50 μm (E-G); 20 μm (H-J); 10 μm (K-N)." figureDoi="10.3897/mycokeys.74.57824.figure8" httpUri="https://binary.pensoft.net/fig/464289" pageId="0" pageNumber="17">8</figureCitation>
). The anamorph of
<taxonomicName lsidName="P. sabinianus" pageId="0" pageNumber="17" rank="species" species="sabinianus">
<emphasis italics="true" pageId="0" pageNumber="17">P. sabinianus</emphasis>
</taxonomicName>
is unknown; our specimen was not isolated in axenic culture and the strains S.M.H. 3807 and S.M.H. 3824 formed only sterile mycelium in vitro (
<bibRefCitation author="Huhndorf, SM" journalOrPublisher="Fungal Diversity" pageId="0" pageNumber="17" pagination="23 - 49" refId="B45" refString="Huhndorf, SM, Fernandez, FA, 2005. Teleomorph-anamorph connections: Chaetosphaeria raciborskii and related species, and their Craspedodidymum -like anamorphs. Fungal Diversity 19: 23 - 49" title="Teleomorph-anamorph connections: Chaetosphaeria raciborskii and related species, and their Craspedodidymum - like anamorphs." volume="19" year="2005">
Huhndorf and
<normalizedToken originalValue="Fernández">Fernandez</normalizedToken>
2005
</bibRefCitation>
).
</paragraph>
</subSubSection>
</treatment>
</document>