Delimitation of central and northern European species of the Phellinus igniarius group (Basidiomycota, Hymenochaetales) based on analysis of ITS and translation elongation factor 1 alpha DNA sequences
Abstract The Phellinus igniarius group comprises several closely related wood-decaying basidiomycetes with poroid hymenophores that are sometimes difficult to identify on a morphological basis. The delimitation of pileate species belonging to the group was the subject of ITS (internal transcribed sp...
Ausführliche Beschreibung
Autor*in: |
Tomšovský, Michal [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2010 |
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Schlagwörter: |
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Anmerkung: |
© German Mycological Society and Springer 2010 |
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Übergeordnetes Werk: |
Enthalten in: Mycological progress - Berlin : Springer, 2002, 9(2010), 3 vom: 19. Feb., Seite 431-445 |
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Übergeordnetes Werk: |
volume:9 ; year:2010 ; number:3 ; day:19 ; month:02 ; pages:431-445 |
Links: |
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DOI / URN: |
10.1007/s11557-009-0653-x |
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Katalog-ID: |
SPR020746091 |
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245 | 1 | 0 | |a Delimitation of central and northern European species of the Phellinus igniarius group (Basidiomycota, Hymenochaetales) based on analysis of ITS and translation elongation factor 1 alpha DNA sequences |
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500 | |a © German Mycological Society and Springer 2010 | ||
520 | |a Abstract The Phellinus igniarius group comprises several closely related wood-decaying basidiomycetes with poroid hymenophores that are sometimes difficult to identify on a morphological basis. The delimitation of pileate species belonging to the group was the subject of ITS (internal transcribed spacer of ribosomal DNA) and tefa (translation elongation factor 1 alpha) DNA sequence analyses applied to specimens from central and northern Europe. The results confirmed the distinctiveness of P. alni, P. igniarius, P. lundellii, P. nigricans, P. populicola, P. tremulae, and P. tuberculosus in Europe. The specimens of the previously distinguished species P. cinereus were found to be identical with either P. nigricans or P. alni. Thus, Phellinus cinereus does not follow the species criteria of phylogenetic species recognition. In addition, a recently described species, P. neolundellii, was grouped within the P. alni clade. The ITS and tefa analyses produced a different topology for P. populicola and P. igniarius. P. alni had the largest spectrum of hosts, including woody plants from nine families, and records on Aesculus hippocastanum and Ulmus glabra are reported for the first time. P. igniarius s.s. has been collected not only on Salix spp. as expected but also, though rarely, on Populus nigra, and it has been observed once on Malus domestica. The host specificity of the remaining species resembles previous data. An additional analysis of basidiospore dimensions did not reveal any differences between P. alni and P. igniarius, but both are distinguishable from those of P. nigricans. | ||
650 | 4 | |a ITS |7 (dpeaa)DE-He213 | |
650 | 4 | |a Translation elongation factor 1 alpha |7 (dpeaa)DE-He213 | |
650 | 4 | |a Spore measurement |7 (dpeaa)DE-He213 | |
700 | 1 | |a Vampola, Petr |4 aut | |
700 | 1 | |a Sedlák, Petr |4 aut | |
700 | 1 | |a Byrtusová, Zuzana |4 aut | |
700 | 1 | |a Jankovský, Libor |4 aut | |
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10.1007/s11557-009-0653-x doi (DE-627)SPR020746091 (SPR)s11557-009-0653-x-e DE-627 ger DE-627 rakwb eng Tomšovský, Michal verfasserin aut Delimitation of central and northern European species of the Phellinus igniarius group (Basidiomycota, Hymenochaetales) based on analysis of ITS and translation elongation factor 1 alpha DNA sequences 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © German Mycological Society and Springer 2010 Abstract The Phellinus igniarius group comprises several closely related wood-decaying basidiomycetes with poroid hymenophores that are sometimes difficult to identify on a morphological basis. The delimitation of pileate species belonging to the group was the subject of ITS (internal transcribed spacer of ribosomal DNA) and tefa (translation elongation factor 1 alpha) DNA sequence analyses applied to specimens from central and northern Europe. The results confirmed the distinctiveness of P. alni, P. igniarius, P. lundellii, P. nigricans, P. populicola, P. tremulae, and P. tuberculosus in Europe. The specimens of the previously distinguished species P. cinereus were found to be identical with either P. nigricans or P. alni. Thus, Phellinus cinereus does not follow the species criteria of phylogenetic species recognition. In addition, a recently described species, P. neolundellii, was grouped within the P. alni clade. The ITS and tefa analyses produced a different topology for P. populicola and P. igniarius. P. alni had the largest spectrum of hosts, including woody plants from nine families, and records on Aesculus hippocastanum and Ulmus glabra are reported for the first time. P. igniarius s.s. has been collected not only on Salix spp. as expected but also, though rarely, on Populus nigra, and it has been observed once on Malus domestica. The host specificity of the remaining species resembles previous data. An additional analysis of basidiospore dimensions did not reveal any differences between P. alni and P. igniarius, but both are distinguishable from those of P. nigricans. ITS (dpeaa)DE-He213 Translation elongation factor 1 alpha (dpeaa)DE-He213 Spore measurement (dpeaa)DE-He213 Vampola, Petr aut Sedlák, Petr aut Byrtusová, Zuzana aut Jankovský, Libor aut Enthalten in Mycological progress Berlin : Springer, 2002 9(2010), 3 vom: 19. Feb., Seite 431-445 (DE-627)509398952 (DE-600)2226747-5 1861-8952 nnns volume:9 year:2010 number:3 day:19 month:02 pages:431-445 https://dx.doi.org/10.1007/s11557-009-0653-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 9 2010 3 19 02 431-445 |
spelling |
10.1007/s11557-009-0653-x doi (DE-627)SPR020746091 (SPR)s11557-009-0653-x-e DE-627 ger DE-627 rakwb eng Tomšovský, Michal verfasserin aut Delimitation of central and northern European species of the Phellinus igniarius group (Basidiomycota, Hymenochaetales) based on analysis of ITS and translation elongation factor 1 alpha DNA sequences 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © German Mycological Society and Springer 2010 Abstract The Phellinus igniarius group comprises several closely related wood-decaying basidiomycetes with poroid hymenophores that are sometimes difficult to identify on a morphological basis. The delimitation of pileate species belonging to the group was the subject of ITS (internal transcribed spacer of ribosomal DNA) and tefa (translation elongation factor 1 alpha) DNA sequence analyses applied to specimens from central and northern Europe. The results confirmed the distinctiveness of P. alni, P. igniarius, P. lundellii, P. nigricans, P. populicola, P. tremulae, and P. tuberculosus in Europe. The specimens of the previously distinguished species P. cinereus were found to be identical with either P. nigricans or P. alni. Thus, Phellinus cinereus does not follow the species criteria of phylogenetic species recognition. In addition, a recently described species, P. neolundellii, was grouped within the P. alni clade. The ITS and tefa analyses produced a different topology for P. populicola and P. igniarius. P. alni had the largest spectrum of hosts, including woody plants from nine families, and records on Aesculus hippocastanum and Ulmus glabra are reported for the first time. P. igniarius s.s. has been collected not only on Salix spp. as expected but also, though rarely, on Populus nigra, and it has been observed once on Malus domestica. The host specificity of the remaining species resembles previous data. An additional analysis of basidiospore dimensions did not reveal any differences between P. alni and P. igniarius, but both are distinguishable from those of P. nigricans. ITS (dpeaa)DE-He213 Translation elongation factor 1 alpha (dpeaa)DE-He213 Spore measurement (dpeaa)DE-He213 Vampola, Petr aut Sedlák, Petr aut Byrtusová, Zuzana aut Jankovský, Libor aut Enthalten in Mycological progress Berlin : Springer, 2002 9(2010), 3 vom: 19. Feb., Seite 431-445 (DE-627)509398952 (DE-600)2226747-5 1861-8952 nnns volume:9 year:2010 number:3 day:19 month:02 pages:431-445 https://dx.doi.org/10.1007/s11557-009-0653-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 9 2010 3 19 02 431-445 |
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10.1007/s11557-009-0653-x doi (DE-627)SPR020746091 (SPR)s11557-009-0653-x-e DE-627 ger DE-627 rakwb eng Tomšovský, Michal verfasserin aut Delimitation of central and northern European species of the Phellinus igniarius group (Basidiomycota, Hymenochaetales) based on analysis of ITS and translation elongation factor 1 alpha DNA sequences 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © German Mycological Society and Springer 2010 Abstract The Phellinus igniarius group comprises several closely related wood-decaying basidiomycetes with poroid hymenophores that are sometimes difficult to identify on a morphological basis. The delimitation of pileate species belonging to the group was the subject of ITS (internal transcribed spacer of ribosomal DNA) and tefa (translation elongation factor 1 alpha) DNA sequence analyses applied to specimens from central and northern Europe. The results confirmed the distinctiveness of P. alni, P. igniarius, P. lundellii, P. nigricans, P. populicola, P. tremulae, and P. tuberculosus in Europe. The specimens of the previously distinguished species P. cinereus were found to be identical with either P. nigricans or P. alni. Thus, Phellinus cinereus does not follow the species criteria of phylogenetic species recognition. In addition, a recently described species, P. neolundellii, was grouped within the P. alni clade. The ITS and tefa analyses produced a different topology for P. populicola and P. igniarius. P. alni had the largest spectrum of hosts, including woody plants from nine families, and records on Aesculus hippocastanum and Ulmus glabra are reported for the first time. P. igniarius s.s. has been collected not only on Salix spp. as expected but also, though rarely, on Populus nigra, and it has been observed once on Malus domestica. The host specificity of the remaining species resembles previous data. An additional analysis of basidiospore dimensions did not reveal any differences between P. alni and P. igniarius, but both are distinguishable from those of P. nigricans. ITS (dpeaa)DE-He213 Translation elongation factor 1 alpha (dpeaa)DE-He213 Spore measurement (dpeaa)DE-He213 Vampola, Petr aut Sedlák, Petr aut Byrtusová, Zuzana aut Jankovský, Libor aut Enthalten in Mycological progress Berlin : Springer, 2002 9(2010), 3 vom: 19. Feb., Seite 431-445 (DE-627)509398952 (DE-600)2226747-5 1861-8952 nnns volume:9 year:2010 number:3 day:19 month:02 pages:431-445 https://dx.doi.org/10.1007/s11557-009-0653-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 9 2010 3 19 02 431-445 |
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10.1007/s11557-009-0653-x doi (DE-627)SPR020746091 (SPR)s11557-009-0653-x-e DE-627 ger DE-627 rakwb eng Tomšovský, Michal verfasserin aut Delimitation of central and northern European species of the Phellinus igniarius group (Basidiomycota, Hymenochaetales) based on analysis of ITS and translation elongation factor 1 alpha DNA sequences 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © German Mycological Society and Springer 2010 Abstract The Phellinus igniarius group comprises several closely related wood-decaying basidiomycetes with poroid hymenophores that are sometimes difficult to identify on a morphological basis. The delimitation of pileate species belonging to the group was the subject of ITS (internal transcribed spacer of ribosomal DNA) and tefa (translation elongation factor 1 alpha) DNA sequence analyses applied to specimens from central and northern Europe. The results confirmed the distinctiveness of P. alni, P. igniarius, P. lundellii, P. nigricans, P. populicola, P. tremulae, and P. tuberculosus in Europe. The specimens of the previously distinguished species P. cinereus were found to be identical with either P. nigricans or P. alni. Thus, Phellinus cinereus does not follow the species criteria of phylogenetic species recognition. In addition, a recently described species, P. neolundellii, was grouped within the P. alni clade. The ITS and tefa analyses produced a different topology for P. populicola and P. igniarius. P. alni had the largest spectrum of hosts, including woody plants from nine families, and records on Aesculus hippocastanum and Ulmus glabra are reported for the first time. P. igniarius s.s. has been collected not only on Salix spp. as expected but also, though rarely, on Populus nigra, and it has been observed once on Malus domestica. The host specificity of the remaining species resembles previous data. An additional analysis of basidiospore dimensions did not reveal any differences between P. alni and P. igniarius, but both are distinguishable from those of P. nigricans. ITS (dpeaa)DE-He213 Translation elongation factor 1 alpha (dpeaa)DE-He213 Spore measurement (dpeaa)DE-He213 Vampola, Petr aut Sedlák, Petr aut Byrtusová, Zuzana aut Jankovský, Libor aut Enthalten in Mycological progress Berlin : Springer, 2002 9(2010), 3 vom: 19. Feb., Seite 431-445 (DE-627)509398952 (DE-600)2226747-5 1861-8952 nnns volume:9 year:2010 number:3 day:19 month:02 pages:431-445 https://dx.doi.org/10.1007/s11557-009-0653-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 9 2010 3 19 02 431-445 |
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10.1007/s11557-009-0653-x doi (DE-627)SPR020746091 (SPR)s11557-009-0653-x-e DE-627 ger DE-627 rakwb eng Tomšovský, Michal verfasserin aut Delimitation of central and northern European species of the Phellinus igniarius group (Basidiomycota, Hymenochaetales) based on analysis of ITS and translation elongation factor 1 alpha DNA sequences 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © German Mycological Society and Springer 2010 Abstract The Phellinus igniarius group comprises several closely related wood-decaying basidiomycetes with poroid hymenophores that are sometimes difficult to identify on a morphological basis. The delimitation of pileate species belonging to the group was the subject of ITS (internal transcribed spacer of ribosomal DNA) and tefa (translation elongation factor 1 alpha) DNA sequence analyses applied to specimens from central and northern Europe. The results confirmed the distinctiveness of P. alni, P. igniarius, P. lundellii, P. nigricans, P. populicola, P. tremulae, and P. tuberculosus in Europe. The specimens of the previously distinguished species P. cinereus were found to be identical with either P. nigricans or P. alni. Thus, Phellinus cinereus does not follow the species criteria of phylogenetic species recognition. In addition, a recently described species, P. neolundellii, was grouped within the P. alni clade. The ITS and tefa analyses produced a different topology for P. populicola and P. igniarius. P. alni had the largest spectrum of hosts, including woody plants from nine families, and records on Aesculus hippocastanum and Ulmus glabra are reported for the first time. P. igniarius s.s. has been collected not only on Salix spp. as expected but also, though rarely, on Populus nigra, and it has been observed once on Malus domestica. The host specificity of the remaining species resembles previous data. An additional analysis of basidiospore dimensions did not reveal any differences between P. alni and P. igniarius, but both are distinguishable from those of P. nigricans. ITS (dpeaa)DE-He213 Translation elongation factor 1 alpha (dpeaa)DE-He213 Spore measurement (dpeaa)DE-He213 Vampola, Petr aut Sedlák, Petr aut Byrtusová, Zuzana aut Jankovský, Libor aut Enthalten in Mycological progress Berlin : Springer, 2002 9(2010), 3 vom: 19. Feb., Seite 431-445 (DE-627)509398952 (DE-600)2226747-5 1861-8952 nnns volume:9 year:2010 number:3 day:19 month:02 pages:431-445 https://dx.doi.org/10.1007/s11557-009-0653-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 9 2010 3 19 02 431-445 |
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Enthalten in Mycological progress 9(2010), 3 vom: 19. Feb., Seite 431-445 volume:9 year:2010 number:3 day:19 month:02 pages:431-445 |
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Mycological progress |
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Tomšovský, Michal @@aut@@ Vampola, Petr @@aut@@ Sedlák, Petr @@aut@@ Byrtusová, Zuzana @@aut@@ Jankovský, Libor @@aut@@ |
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2010-02-19T00:00:00Z |
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The delimitation of pileate species belonging to the group was the subject of ITS (internal transcribed spacer of ribosomal DNA) and tefa (translation elongation factor 1 alpha) DNA sequence analyses applied to specimens from central and northern Europe. The results confirmed the distinctiveness of P. alni, P. igniarius, P. lundellii, P. nigricans, P. populicola, P. tremulae, and P. tuberculosus in Europe. The specimens of the previously distinguished species P. cinereus were found to be identical with either P. nigricans or P. alni. Thus, Phellinus cinereus does not follow the species criteria of phylogenetic species recognition. In addition, a recently described species, P. neolundellii, was grouped within the P. alni clade. The ITS and tefa analyses produced a different topology for P. populicola and P. igniarius. P. alni had the largest spectrum of hosts, including woody plants from nine families, and records on Aesculus hippocastanum and Ulmus glabra are reported for the first time. P. igniarius s.s. has been collected not only on Salix spp. as expected but also, though rarely, on Populus nigra, and it has been observed once on Malus domestica. The host specificity of the remaining species resembles previous data. An additional analysis of basidiospore dimensions did not reveal any differences between P. alni and P. igniarius, but both are distinguishable from those of P. nigricans.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">ITS</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Translation elongation factor 1 alpha</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Spore measurement</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Vampola, Petr</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Sedlák, Petr</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Byrtusová, Zuzana</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Jankovský, Libor</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Mycological progress</subfield><subfield code="d">Berlin : Springer, 2002</subfield><subfield code="g">9(2010), 3 vom: 19. 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Tomšovský, Michal |
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Tomšovský, Michal misc ITS misc Translation elongation factor 1 alpha misc Spore measurement Delimitation of central and northern European species of the Phellinus igniarius group (Basidiomycota, Hymenochaetales) based on analysis of ITS and translation elongation factor 1 alpha DNA sequences |
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Delimitation of central and northern European species of the Phellinus igniarius group (Basidiomycota, Hymenochaetales) based on analysis of ITS and translation elongation factor 1 alpha DNA sequences ITS (dpeaa)DE-He213 Translation elongation factor 1 alpha (dpeaa)DE-He213 Spore measurement (dpeaa)DE-He213 |
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Delimitation of central and northern European species of the Phellinus igniarius group (Basidiomycota, Hymenochaetales) based on analysis of ITS and translation elongation factor 1 alpha DNA sequences |
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Delimitation of central and northern European species of the Phellinus igniarius group (Basidiomycota, Hymenochaetales) based on analysis of ITS and translation elongation factor 1 alpha DNA sequences |
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Tomšovský, Michal |
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Tomšovský, Michal Vampola, Petr Sedlák, Petr Byrtusová, Zuzana Jankovský, Libor |
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title_sort |
delimitation of central and northern european species of the phellinus igniarius group (basidiomycota, hymenochaetales) based on analysis of its and translation elongation factor 1 alpha dna sequences |
title_auth |
Delimitation of central and northern European species of the Phellinus igniarius group (Basidiomycota, Hymenochaetales) based on analysis of ITS and translation elongation factor 1 alpha DNA sequences |
abstract |
Abstract The Phellinus igniarius group comprises several closely related wood-decaying basidiomycetes with poroid hymenophores that are sometimes difficult to identify on a morphological basis. The delimitation of pileate species belonging to the group was the subject of ITS (internal transcribed spacer of ribosomal DNA) and tefa (translation elongation factor 1 alpha) DNA sequence analyses applied to specimens from central and northern Europe. The results confirmed the distinctiveness of P. alni, P. igniarius, P. lundellii, P. nigricans, P. populicola, P. tremulae, and P. tuberculosus in Europe. The specimens of the previously distinguished species P. cinereus were found to be identical with either P. nigricans or P. alni. Thus, Phellinus cinereus does not follow the species criteria of phylogenetic species recognition. In addition, a recently described species, P. neolundellii, was grouped within the P. alni clade. The ITS and tefa analyses produced a different topology for P. populicola and P. igniarius. P. alni had the largest spectrum of hosts, including woody plants from nine families, and records on Aesculus hippocastanum and Ulmus glabra are reported for the first time. P. igniarius s.s. has been collected not only on Salix spp. as expected but also, though rarely, on Populus nigra, and it has been observed once on Malus domestica. The host specificity of the remaining species resembles previous data. An additional analysis of basidiospore dimensions did not reveal any differences between P. alni and P. igniarius, but both are distinguishable from those of P. nigricans. © German Mycological Society and Springer 2010 |
abstractGer |
Abstract The Phellinus igniarius group comprises several closely related wood-decaying basidiomycetes with poroid hymenophores that are sometimes difficult to identify on a morphological basis. The delimitation of pileate species belonging to the group was the subject of ITS (internal transcribed spacer of ribosomal DNA) and tefa (translation elongation factor 1 alpha) DNA sequence analyses applied to specimens from central and northern Europe. The results confirmed the distinctiveness of P. alni, P. igniarius, P. lundellii, P. nigricans, P. populicola, P. tremulae, and P. tuberculosus in Europe. The specimens of the previously distinguished species P. cinereus were found to be identical with either P. nigricans or P. alni. Thus, Phellinus cinereus does not follow the species criteria of phylogenetic species recognition. In addition, a recently described species, P. neolundellii, was grouped within the P. alni clade. The ITS and tefa analyses produced a different topology for P. populicola and P. igniarius. P. alni had the largest spectrum of hosts, including woody plants from nine families, and records on Aesculus hippocastanum and Ulmus glabra are reported for the first time. P. igniarius s.s. has been collected not only on Salix spp. as expected but also, though rarely, on Populus nigra, and it has been observed once on Malus domestica. The host specificity of the remaining species resembles previous data. An additional analysis of basidiospore dimensions did not reveal any differences between P. alni and P. igniarius, but both are distinguishable from those of P. nigricans. © German Mycological Society and Springer 2010 |
abstract_unstemmed |
Abstract The Phellinus igniarius group comprises several closely related wood-decaying basidiomycetes with poroid hymenophores that are sometimes difficult to identify on a morphological basis. The delimitation of pileate species belonging to the group was the subject of ITS (internal transcribed spacer of ribosomal DNA) and tefa (translation elongation factor 1 alpha) DNA sequence analyses applied to specimens from central and northern Europe. The results confirmed the distinctiveness of P. alni, P. igniarius, P. lundellii, P. nigricans, P. populicola, P. tremulae, and P. tuberculosus in Europe. The specimens of the previously distinguished species P. cinereus were found to be identical with either P. nigricans or P. alni. Thus, Phellinus cinereus does not follow the species criteria of phylogenetic species recognition. In addition, a recently described species, P. neolundellii, was grouped within the P. alni clade. The ITS and tefa analyses produced a different topology for P. populicola and P. igniarius. P. alni had the largest spectrum of hosts, including woody plants from nine families, and records on Aesculus hippocastanum and Ulmus glabra are reported for the first time. P. igniarius s.s. has been collected not only on Salix spp. as expected but also, though rarely, on Populus nigra, and it has been observed once on Malus domestica. The host specificity of the remaining species resembles previous data. An additional analysis of basidiospore dimensions did not reveal any differences between P. alni and P. igniarius, but both are distinguishable from those of P. nigricans. © German Mycological Society and Springer 2010 |
collection_details |
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container_issue |
3 |
title_short |
Delimitation of central and northern European species of the Phellinus igniarius group (Basidiomycota, Hymenochaetales) based on analysis of ITS and translation elongation factor 1 alpha DNA sequences |
url |
https://dx.doi.org/10.1007/s11557-009-0653-x |
remote_bool |
true |
author2 |
Vampola, Petr Sedlák, Petr Byrtusová, Zuzana Jankovský, Libor |
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Vampola, Petr Sedlák, Petr Byrtusová, Zuzana Jankovský, Libor |
ppnlink |
509398952 |
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hochschulschrift_bool |
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doi_str |
10.1007/s11557-009-0653-x |
up_date |
2024-07-03T18:00:46.783Z |
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score |
7.400257 |