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<document id="C76E1E07C1DCCF5E524B0A5EDF9A069F" ID-DOI="http://dx.doi.org/10.3897/mycokeys.50.32432" ID-GBIF-Dataset="059c89da-7ae5-4dbb-b876-bd1617110873" ID-PMC="PMC6477855" ID-Pensoft-Pub="1314-4049-50-1" ID-PubMed="31043855" ModsDocAuthor="" ModsDocDate="2019" ModsDocID="1314-4049-50-1" ModsDocOrigin="MycoKeys 50" ModsDocTitle="Solving the taxonomic identity of Pseudotomentellatristis s.l. (Thelephorales, Basidiomycota) a multi-gene phylogeny and taxonomic review, integrating ecological and geographical data" checkinTime="1555333405629" checkinUser="pensoft" docAuthor="Svantesson, Sten, Larsson, Karl-Henrik, Koljalg, Urmas, W. May, Tom, Patrik Cangren,, Henrik Nilsson, R. &amp; Larsson, Ellen" docDate="2019" docId="0BC919E3181EECF16FE62CE43865E3E3" docLanguage="en" docName="MycoKeys 50: 1-77" docOrigin="MycoKeys 50" docSource="http://dx.doi.org/10.3897/mycokeys.50.32432" docTitle="Pseudotomentella alobata Svantesson, sp. nov." docType="treatment" docVersion="5" lastPageNumber="22" masterDocId="BF413468CD59FFA53A5DFFC1FF9F272E" masterDocTitle="Solving the taxonomic identity of Pseudotomentellatristis s. l. (Thelephorales, Basidiomycota) - a multi-gene phylogeny and taxonomic review, integrating ecological and geographical data" masterLastPageNumber="77" masterPageNumber="1" pageNumber="21" updateTime="1732478795134" updateUser="ExternalLinkService">
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<mods:title id="FDC9E12C321E582AC461810203F632C4">Solving the taxonomic identity of Pseudotomentellatristis s. l. (Thelephorales, Basidiomycota) - a multi-gene phylogeny and taxonomic review, integrating ecological and geographical data</mods:title>
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<mods:namePart id="0327E727B35EB3247FF08552DB821CCA">Svantesson, Sten</mods:namePart>
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<mods:namePart id="C8D8963CCA4288EAAD73B3C033C38647">Larsson, Karl-Henrik</mods:namePart>
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<mods:namePart id="F6507F40478F54CDD08BB12BAC738949">Koljalg, Urmas</mods:namePart>
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<mods:namePart id="D38187FEC452DC1B75FEB1CA1B1A8F7F">Patrik Cangren,</mods:namePart>
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<treatment id="0BC919E3181EECF16FE62CE43865E3E3" ID-GBIF-Taxon="156201988" LSID="urn:lsid:plazi:treatment:0BC919E3181EECF16FE62CE43865E3E3" httpUri="http://treatment.plazi.org/id/0BC919E3181EECF16FE62CE43865E3E3" lastPageId="21" lastPageNumber="22" pageId="20" pageNumber="21" scope_order="Thelephorales" scope_phylum="Basidiomycota">
<subSubSection id="2040A5E13108388477935589045C13F3" pageId="20" pageNumber="21" type="nomenclature">
<paragraph id="CB4924C71693167A601BEE65D8B7FC10" pageId="20" pageNumber="21">
<taxonomicName id="E17423CB0E850D53021EED210D9392B9" ID-CoL="4PDR7" LSID="MB828999" authority="Svantesson" class="Agaricomycetes" family="Thelephoraceae" genus="Pseudotomentella" higherTaxonomySource="CoL" kingdom="Fungi" lsidName="Pseudotomentella alobata" order="Thelephorales" pageId="20" pageNumber="21" phylum="Basidiomycota" rank="species" species="alobata">Pseudotomentella alobata Svantesson</taxonomicName>
<taxonomicNameLabel id="D2E56583FDA81259853B58F6D8331FF6" pageId="20" pageNumber="21">sp. nov.</taxonomicNameLabel>
Fig. 9
</paragraph>
</subSubSection>
<subSubSection id="026C3EB449BC450C538F0D43E6E439D6" pageId="20" pageNumber="21" type="materials_examined">
<paragraph id="4F3B835776C1D6467EA0950CFBE07211" pageId="20" pageNumber="21">Type.</paragraph>
<paragraph id="F453C8C43990DD7D1E3B2AA19C88C089" pageId="20" pageNumber="21">
SWEDEN. Dalsland, Mellerud,
<normalizedToken id="31906F9E0F546A6A3F80937D72B9D191" originalValue="Skållerud">Skallerud</normalizedToken>
, Norgekullen SW, coniferous forest on soil with high pH, 20 September 2017, S. Svantesson 425 (holotype: GB!, GenBank Acc. No. ITS: MK290696).
</paragraph>
</subSubSection>
<subSubSection id="916395037746796F2BB0CB7373BD069C" pageId="20" pageNumber="21" type="unite sh">
<paragraph id="AC9F4CE2F532238C13A1D12DE6598332" pageId="20" pageNumber="21">UNITE SH.</paragraph>
<paragraph id="A7B81D461915FDDB895B387AEE739BB4" pageId="20" pageNumber="21">SH030577.07FU</paragraph>
</subSubSection>
<subSubSection id="14DE14AA76B3A05328C66A7F9A801F03" pageId="20" pageNumber="21" type="etymology">
<paragraph id="98DCE1D927B72AA4B3E79E12CD40675B" pageId="20" pageNumber="21">Etymology.</paragraph>
<paragraph id="C746ECD52AF39F77F8FA25971B85002C" pageId="20" pageNumber="21">The name refers to the spores, which commonly lack lobation.</paragraph>
</subSubSection>
<subSubSection id="A5B9BEF847EDCE22AE203E9CE4CCB4E7" lastPageId="21" lastPageNumber="22" pageId="20" pageNumber="21" type="description">
<paragraph id="C332EF4333BF4FCECF9A382603A92DC1" pageId="20" pageNumber="21">Description.</paragraph>
<paragraph id="107607E9F4535D144D9D04AEB3077F67" pageId="20" pageNumber="21">Basidiomata annual, resupinate, membranaceous, effused - often to several tens of centimetres in diameter. Mature parts continuous, with a cottony texture when fresh and a rather firm, fibrous and compact, yet quite soft and elastic texture when dried. Hymenium smooth, but sometimes strongly undulating; brown, purplish-brown or blue-greyish-brown when fresh, brown with a pinkish hue when dried. Immature parts discontinuous, byssoid, with a cottony texture both when fresh and when dried. Subhymenium and hymenium of immature parts blue to blue grey when fresh and blue grey to brown grey when dried. Subiculum well developed, loose, fibrous, orange brown; often forms the outer edge of basidiomata, extending noticeably beyond the hymenium.</paragraph>
<caption id="E6951A06BEE9810C16C08CDB854052A6" pageId="20" pageNumber="21">
<paragraph id="E874F48ECEF86ECFCBF057E28A01890D" pageId="20" pageNumber="21">
Figure 9. Morphological features of
<taxonomicName id="AC79336EF2607E6EAB065EAB000C8379" lsidName="P. alobata" pageId="20" pageNumber="21" rank="species" species="alobata">P. alobata</taxonomicName>
, mounted in KOH and macroscopically. A, B basidiospores in frontal face (O F110315) C, D in lateral face (O F110316) E subicular hyphae (TU 115626) F mature basidiome (holotype).
</paragraph>
</caption>
<paragraph id="0AA8FB9B990818BC29C06CD273333DD1" pageId="20" pageNumber="21">Hyphal cords lacking, but loose bundles of subicular hyphae sometimes present.</paragraph>
<paragraph id="773AA7CB5E325F27A31F158D36903A7B" pageId="20" pageNumber="21">Hyphal system monomitic, clamp connections absent from all hyphae.</paragraph>
<paragraph id="E7858C8F1634FFE9916A5FE135D8F9C7" pageId="20" pageNumber="21">
Subicular hyphae noticeably long and straight, thick-walled; forming a loose tissue. Individual hyphae (4.3-) 4.6-7.4 (-7.6)
<normalizedToken id="B0C33FC1FECAB35B4F1C866C8EF3866E" originalValue="μm">μm</normalizedToken>
wide, with a mean width of 5.6-5.9
<normalizedToken id="494F0BF766C996C3C367108FFA5242B4" originalValue="μm">μm</normalizedToken>
; orange in both KOH and water.
</paragraph>
<paragraph id="FBE2B2E32DF28894741C6D83BB1945C0" pageId="20" pageNumber="21">
Subhymenial hyphae often somewhat sinuous, thin to thick-walled; forming a rather dense tissue. Individual hyphae (3.1-) 3.4-6.9
<normalizedToken id="72853593931B9A8A4909E55C353F2E7C" originalValue="μm">μm</normalizedToken>
wide, with a mean width of 4.0-4.5
<normalizedToken id="72FECBD664AA2EB2C89538C99B42683E" originalValue="μm">μm</normalizedToken>
; hyaline to pale green in KOH, blue green in the presence of air; yellow to pale orange yellow in water, with strongly granular contents.
</paragraph>
<paragraph id="11E4E460D3510B268DB9A74A6ACCB06A" pageId="20" pageNumber="21">Encrustation granular, amyloid; purple in KOH, dark blue green in the presence of air; dark brown in water; usually common and scattered in occurrence on the upper parts of subhymenial hyphae and on the lower parts of basidia.</paragraph>
<paragraph id="8298EFF9C0018AA256FFD9F168311DF4" pageId="20" pageNumber="21">
Basidia with four slightly curved sterigmata, occasionally two-sterigmate; clavate to narrowly clavate, sometimes clavopedunculate, thin-walled, with one-three slight constrictions. Dimensions: (63-) 64-91 (-98)
<normalizedToken id="4E40ED1E54E1BF45B007B97C41908609" originalValue="×">x</normalizedToken>
(10.2-) 10.5-14.2 (-14.3)
<normalizedToken id="19F6E3C14C201F2B1AAAF5B296C09906" originalValue="μm">μm</normalizedToken>
; mean dimensions: 74-77
<normalizedToken id="9C11295F2A9227C3DD0CEF1BDD645114" originalValue="×">x</normalizedToken>
11.3-12.1
<normalizedToken id="F805BB4643513747DFC0F54FB1B476D3" originalValue="μm">μm</normalizedToken>
. Sterigmata 8.5-12.1 (-12.4)
<normalizedToken id="14CC7623E12B1564EBFAE0486E7A620B" originalValue="μm">μm</normalizedToken>
long, with a mean length of 10.0-10.3
<normalizedToken id="B2611FD4E086949492C16C6595A090D5" originalValue="μm">μm</normalizedToken>
. Colours and reactions the same as for the subhymenial hyphae, but in addition often with granular contents in KOH.
</paragraph>
<paragraph id="3DE7E3F69EAEFC175DA53A838A867DDB" pageId="20" pageNumber="21">Cystidial organs lacking.</paragraph>
<paragraph id="2FFAF21C4771E1259BB6A78280045809" lastPageId="21" lastPageNumber="22" pageId="20" pageNumber="21">
Basidiospores in frontal face generally with a subcircular basic shape and an unlobed or occasionally weakly pronounced, rounded, heart-shaped outline, covered in bi- or trifurcate, sometimes singularly attached, echinuli. Subcircular, three-five-lobed spores infrequently occurring, as well as abnormally large spores originating from two-sterigmate basidia. Frontal dimensions: (9.0-) 9.1-10.7
<normalizedToken id="42446DFE3292411FBBCEEA7E204E9C8D" originalValue="×">x</normalizedToken>
(8.4-) 8.9-10.5 (-10.7)
<normalizedToken id="CF7EB6EC639AB1D06C9357CCCF631AAD" originalValue="μm">μm</normalizedToken>
; mean dimensions: 9.7-10.1
<normalizedToken id="F3763CC5A677FB434356E56EAE5EA2A7" originalValue="×">x</normalizedToken>
9.5-9.8
<normalizedToken id="4FA8BEB00D04832299E04A7751954A84" originalValue="μm">μm</normalizedToken>
; Q-value: (0.9-) 1.0-1.1; mean Q-value: 1.0. Echinuli 1.2-1.8 (-1.9)
<normalizedToken id="27233DD50C54BBCE31384D149861F494" originalValue="μm">μm</normalizedToken>
long, with a mean length of 1.4-1.7
<normalizedToken id="A82F227437474B27331271B1BF1EC8A8" originalValue="μm">μm</normalizedToken>
. Lat
<pageBreakToken id="1DC4F30C50A6C0ED947EBBBEFBBD12DD" pageId="21" pageNumber="22" start="start">eral</pageBreakToken>
face ellipsoid, usually with evenly rounded edges, sometimes with one-three lobes. Lateral dimensions: (8.9-) 9.1-10.3
<normalizedToken id="3D26F5E24DCDE2F2A22817852D86000A" originalValue="×">x</normalizedToken>
(6.5-) 6.7-8.2
<normalizedToken id="8923C8EE8BCA99518294FA1118B1B1DB" originalValue="μm">μm</normalizedToken>
; mean dimensions: 9.7-9.9
<normalizedToken id="18E62309B621C8BCD02ECC4FE12744EB" originalValue="×">x</normalizedToken>
7.1-7.4
<normalizedToken id="E27F64B8F8A7C3CD0E16EB68DA88B99C" originalValue="μm">μm</normalizedToken>
; Q-value: (1.2-) 1.3-1.5; mean Q-value: 1.3-1.4. Colour in KOH pale brownish-yellow, in the presence of air often with a blue green reaction; in water pale greenish-yellow to pale orange yellow; occasionally amyloid.
</paragraph>
<paragraph id="E595BDD6B10D0478C40687E44B48172B" pageId="21" pageNumber="22">Chlamydospores lacking.</paragraph>
</subSubSection>
<subSubSection id="50C3C8BB703FFB932E2B07B8F13E373A" pageId="21" pageNumber="22" type="habitat">
<paragraph id="E367C82FA2790F1F1A44A8102195FDA3" pageId="21" pageNumber="22">Habitat.</paragraph>
<paragraph id="573241012CBD65D44862727B3CC5C935" pageId="21" pageNumber="22">Data on habitat are scarce to date, but recent Scandinavian collections have been made in old growth coniferous or mixed forests on soil with high pH.</paragraph>
</subSubSection>
<subSubSection id="AE4F42BF0E4580782D17B399A6C4DAC4" pageId="21" pageNumber="22" type="distribution">
<paragraph id="0B62BF4D2C45928900E2312F96D9B9EF" pageId="21" pageNumber="22">Distribution.</paragraph>
<paragraph id="BB8F34B0DD0B9C60B02644EEBD4195D6" pageId="21" pageNumber="22">Basidiomata encountered in: Norway, Slovenia and Sweden. No sequences originating from soil or root tip samples in UNITE.</paragraph>
</subSubSection>
<subSubSection id="1FA29E0BAF6D8BC1F8AF70E3DBA786CE" pageId="21" pageNumber="22" type="remarks">
<paragraph id="6141E0D02B89E7E241DC42ABAD6ED5FD" pageId="21" pageNumber="22">Remarks.</paragraph>
<paragraph id="21382B2B89DFCDEAFC499A51BCD9AFF0" pageId="21" pageNumber="22">
Within the
<taxonomicName id="8BD4F8959DBA42DC961EA9E101F7E726" lsidName="P. tristis" pageId="21" pageNumber="22" rank="species" species="tristis">P. tristis</taxonomicName>
group, the basidiomata of
<taxonomicName id="1D281021192FC8A926B1497AA4A9D660" lsidName="P. alobata" pageId="21" pageNumber="22" rank="species" species="alobata">P. alobata</taxonomicName>
are recognised by their lack of hyphal cords and skeletal hyphae and their soft, yet rather firm and compact and
<normalizedToken id="427C5F683A1F599AB83826BC392AB6C8" originalValue="±">+/-</normalizedToken>
elastic texture after drying, bluish to greenish colour of immature parts, wide subicular hyphae, long, unlobed spores and amyloid encrustation on subhymenial hyphae and basidia.
<taxonomicName id="A30FCC1E3BF408BDF8840FD8863612CD" class="Agaricomycetes" family="Thelephoraceae" genus="Pseudotomentella" higherTaxonomySource="CoL" kingdom="Fungi" lsidName="Pseudotomentella abundiloba" order="Thelephorales" pageId="21" pageNumber="22" phylum="Basidiomycota" rank="species" species="abundiloba">Pseudotomentella abundiloba</taxonomicName>
,
<taxonomicName id="D22C588927A690FEBF9A069B7AEDF83E" lsidName="P. pluriloba" pageId="21" pageNumber="22" rank="species" species="pluriloba">P. pluriloba</taxonomicName>
and
<taxonomicName id="513FD8F35AE0F08DC66BFBAABDF8959F" lsidName="P. media" pageId="21" pageNumber="22" rank="species" species="media">P. media</taxonomicName>
can appear similar, but none of them has spores which generally are unlobed.
<taxonomicName id="C20BFA894DF4530A24E6298FC014B569" lsidName="P. media" pageId="21" pageNumber="22" rank="species" species="media">P. media</taxonomicName>
further differs by having smaller spores and narrower subicular hyphae, while
<taxonomicName id="352DEC45B5DE4F274CE9746CAEFFAFE1" lsidName="P. pluriloba" pageId="21" pageNumber="22" rank="species" species="pluriloba">P. pluriloba</taxonomicName>
has narrower subicular hyphae, longer sterigmata and frontally wider spores than
<taxonomicName id="B7EC841D0C661F907B2CE287349D1E33" lsidName="P. alobata" pageId="21" pageNumber="22" rank="species" species="alobata">P. alobata</taxonomicName>
.
<taxonomicName id="EAF6985B3C74BD2BDB9C375D2CC8C559" class="Agaricomycetes" family="Thelephoraceae" genus="Pseudotomentella" higherTaxonomySource="CoL" kingdom="Fungi" lsidName="Pseudotomentella abundiloba" order="Thelephorales" pageId="21" pageNumber="22" phylum="Basidiomycota" rank="species" species="abundiloba">Pseudotomentella abundiloba</taxonomicName>
sometimes has encrusted subhymenial hyphae and basidia, but without amyloid reaction.
</paragraph>
</subSubSection>
<subSubSection id="D116D3F891A391A57030D85D50DC4FDE" pageId="21" pageNumber="22" type="additional specimens studied">
<paragraph id="DC5D746C79FD3FA19B688F8289171ACC" pageId="21" pageNumber="22">Additional specimens studied.</paragraph>
<paragraph id="431B17DCCFE2AB76F7039CB6F9E73F6D" pageId="21" pageNumber="22">NORWAY. Telemark: Bamble, Rognsflaugane, boreonemoral, mixed forest on soil with high pH, 2 September 2010, K.-H. Larsson and S. Svantesson (O F110316*); Telemark: Tokke, Dalen, Huvestad, boreonemoral, mixed forest on soil with high pH, 28 September 2010, S. Svantesson and N. Svensson (O F110315*);</paragraph>
<paragraph id="44DD8D1349F7B95C0931622217F5AD6C" pageId="21" pageNumber="22">
SLOVENIA. Radovljica: Triglav National Park, Pokljuka plateau, transition zone between secondary spruce forest (in parts with remnants of primary
<taxonomicName id="FACC139E1F5E4221D919F3A8202001C4" class="Magnoliopsida" family="Fagaceae" genus="Fagus" higherTaxonomySource="CoL" kingdom="Plantae" lsidName="Fagus sylvatica" order="Fagales" pageId="21" pageNumber="22" phylum="Tracheophyta" rank="species" species="sylvatica">Fagus sylvatica</taxonomicName>
/Acer pseudoplatanus forest) and natural
<taxonomicName id="945C32A1687C4206C8035609C4804BFA" class="Pinopsida" family="Pinaceae" genus="Larix" higherTaxonomySource="CoL" kingdom="Plantae" lsidName="Larix decidua" order="Pinales" pageId="21" pageNumber="22" phylum="Tracheophyta" rank="species" species="decidua">Larix decidua</taxonomicName>
stand with individual trees of
<taxonomicName id="24566330FCF4144865DE7E77A16713E9" class="Pinopsida" family="Pinaceae" genus="Pinus" higherTaxonomySource="CoL" kingdom="Plantae" lsidName="Pinus mugo" order="Pinales" pageId="21" pageNumber="22" phylum="Tracheophyta" rank="species" species="mugo">Pinus mugo</taxonomicName>
,
<taxonomicName id="B9F8F32E51E0D03C44C87377BEF8A39F" class="Magnoliopsida" family="Rosaceae" genus="Sorbus" higherTaxonomySource="CoL" kingdom="Plantae" lsidName="Sorbus aucuparia" order="Rosales" pageId="21" pageNumber="22" phylum="Tracheophyta" rank="species" species="aucuparia">Sorbus aucuparia</taxonomicName>
and
<taxonomicName id="EEEB8EC27D286BE9D1D324B049979040" class="Ascidiacea" family="Polycitoridae" genus="Salix" higherTaxonomySource="CoL" kingdom="Animalia" lsidName="Salix" order="Aplousobranchia" pageId="21" pageNumber="22" phylum="Chordata" rank="genus">Salix</taxonomicName>
sp., 1530 m a.s.l., 20 September 2012, U.
<normalizedToken id="B173695823FAAFE5D83FF2EF4D11CF83" originalValue="Kõljalg">Koljalg</normalizedToken>
(TU 115626*);
</paragraph>
<paragraph id="6927209378B9444846090E0443D082A2" pageId="21" pageNumber="22">
SWEDEN.
<normalizedToken id="085BA96CC870A5A3CC7EB710E9A98126" originalValue="Ångermanland">Angermanland</normalizedToken>
: Edsele, Djupdalsmyran, Stordjupdalen, on
<taxonomicName id="D4A7B48EFAFEB7A4FD1295ED5DE14B55" class="Pinopsida" family="Pinaceae" genus="Picea" higherTaxonomySource="CoL" kingdom="Plantae" lsidName="Picea abies" order="Pinales" pageId="21" pageNumber="22" phylum="Tracheophyta" rank="species" species="abies">Picea abies</taxonomicName>
, 29 August 2002, K.-H. Larsson 11873* (GB 0087566).
</paragraph>
</subSubSection>
</treatment>
</document>