A revision of Boletellus sect. Ixocephali

Abstract Taxa included in Boletellus section Ixocephali sensu Singer are re-evaluated and species limits are clarified in a morphological context. In this revision, we recognize four distinct morphological species: B. jalapensis, B. elatus, B. longicollis, and B. singerii. Among these, we have ascer...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Halling, Roy E. [verfasserIn] Ortiz-Santana, Beatriz

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2009

Schlagwörter:	Concept Drift Clamp Connection Tramal Unpaved Road Spore Morphology

Anmerkung:	© German Mycological Society and Springer 2009

Übergeordnetes Werk:	Enthalten in: Mycological progress - Berlin : Springer, 2002, 8(2009), 3 vom: 16. Apr.
Übergeordnetes Werk:	volume:8 ; year:2009 ; number:3 ; day:16 ; month:04

Links:	Volltext

DOI / URN:	10.1007/s11557-009-0595-3

Katalog-ID:	SPR02074546X

Internformat


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520			\|a Abstract Taxa included in Boletellus section Ixocephali sensu Singer are re-evaluated and species limits are clarified in a morphological context. In this revision, we recognize four distinct morphological species: B. jalapensis, B. elatus, B. longicollis, and B. singerii. Among these, we have ascertained that the concept of B. jalapensis was broadened to include another taxon (B. singerii) that was eventually recognized as distinct. Details of spore morphology that include size and shape also show that the precise longitudinal alignment and apical fusion or non-fusion of the costate ornamentation distinguishes two species pairs. These pairs occur on either side of the Pacific basin and include one velate and one non-velate species each: B. longicollis, B. elatus (E Asia) and B. jalapensis, B. singerii (America). Now that discrete morphological entities are clarified and recognizable, phylogenetic hypotheses can be attempted to test these concepts and perhaps infer the monophyly of section Ixocephali when appropriate sequence data are available from newly collected, properly vouchered and viable specimens.
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912			\|a GBV_ILN_138
912			\|a GBV_ILN_150
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912			\|a GBV_ILN_161
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912			\|a GBV_ILN_213
912			\|a GBV_ILN_224
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912			\|a GBV_ILN_702
912			\|a GBV_ILN_2001
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912			\|a GBV_ILN_2004
912			\|a GBV_ILN_2005
912			\|a GBV_ILN_2006
912			\|a GBV_ILN_2007
912			\|a GBV_ILN_2008
912			\|a GBV_ILN_2009
912			\|a GBV_ILN_2010
912			\|a GBV_ILN_2011
912			\|a GBV_ILN_2014
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matchkey_str	article:18618952:2009----::rvsoobltlusc
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publishDate	2009
allfields	10.1007/s11557-009-0595-3 doi (DE-627)SPR02074546X (SPR)s11557-009-0595-3-e DE-627 ger DE-627 rakwb eng Halling, Roy E. verfasserin aut A revision of Boletellus sect. Ixocephali 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © German Mycological Society and Springer 2009 Abstract Taxa included in Boletellus section Ixocephali sensu Singer are re-evaluated and species limits are clarified in a morphological context. In this revision, we recognize four distinct morphological species: B. jalapensis, B. elatus, B. longicollis, and B. singerii. Among these, we have ascertained that the concept of B. jalapensis was broadened to include another taxon (B. singerii) that was eventually recognized as distinct. Details of spore morphology that include size and shape also show that the precise longitudinal alignment and apical fusion or non-fusion of the costate ornamentation distinguishes two species pairs. These pairs occur on either side of the Pacific basin and include one velate and one non-velate species each: B. longicollis, B. elatus (E Asia) and B. jalapensis, B. singerii (America). Now that discrete morphological entities are clarified and recognizable, phylogenetic hypotheses can be attempted to test these concepts and perhaps infer the monophyly of section Ixocephali when appropriate sequence data are available from newly collected, properly vouchered and viable specimens. Concept Drift (dpeaa)DE-He213 Clamp Connection (dpeaa)DE-He213 Tramal (dpeaa)DE-He213 Unpaved Road (dpeaa)DE-He213 Spore Morphology (dpeaa)DE-He213 Ortiz-Santana, Beatriz aut Enthalten in Mycological progress Berlin : Springer, 2002 8(2009), 3 vom: 16. Apr. (DE-627)509398952 (DE-600)2226747-5 1861-8952 nnns volume:8 year:2009 number:3 day:16 month:04 https://dx.doi.org/10.1007/s11557-009-0595-3 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 8 2009 3 16 04
spelling	10.1007/s11557-009-0595-3 doi (DE-627)SPR02074546X (SPR)s11557-009-0595-3-e DE-627 ger DE-627 rakwb eng Halling, Roy E. verfasserin aut A revision of Boletellus sect. Ixocephali 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © German Mycological Society and Springer 2009 Abstract Taxa included in Boletellus section Ixocephali sensu Singer are re-evaluated and species limits are clarified in a morphological context. In this revision, we recognize four distinct morphological species: B. jalapensis, B. elatus, B. longicollis, and B. singerii. Among these, we have ascertained that the concept of B. jalapensis was broadened to include another taxon (B. singerii) that was eventually recognized as distinct. Details of spore morphology that include size and shape also show that the precise longitudinal alignment and apical fusion or non-fusion of the costate ornamentation distinguishes two species pairs. These pairs occur on either side of the Pacific basin and include one velate and one non-velate species each: B. longicollis, B. elatus (E Asia) and B. jalapensis, B. singerii (America). Now that discrete morphological entities are clarified and recognizable, phylogenetic hypotheses can be attempted to test these concepts and perhaps infer the monophyly of section Ixocephali when appropriate sequence data are available from newly collected, properly vouchered and viable specimens. Concept Drift (dpeaa)DE-He213 Clamp Connection (dpeaa)DE-He213 Tramal (dpeaa)DE-He213 Unpaved Road (dpeaa)DE-He213 Spore Morphology (dpeaa)DE-He213 Ortiz-Santana, Beatriz aut Enthalten in Mycological progress Berlin : Springer, 2002 8(2009), 3 vom: 16. Apr. (DE-627)509398952 (DE-600)2226747-5 1861-8952 nnns volume:8 year:2009 number:3 day:16 month:04 https://dx.doi.org/10.1007/s11557-009-0595-3 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 8 2009 3 16 04
allfields_unstemmed	10.1007/s11557-009-0595-3 doi (DE-627)SPR02074546X (SPR)s11557-009-0595-3-e DE-627 ger DE-627 rakwb eng Halling, Roy E. verfasserin aut A revision of Boletellus sect. Ixocephali 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © German Mycological Society and Springer 2009 Abstract Taxa included in Boletellus section Ixocephali sensu Singer are re-evaluated and species limits are clarified in a morphological context. In this revision, we recognize four distinct morphological species: B. jalapensis, B. elatus, B. longicollis, and B. singerii. Among these, we have ascertained that the concept of B. jalapensis was broadened to include another taxon (B. singerii) that was eventually recognized as distinct. Details of spore morphology that include size and shape also show that the precise longitudinal alignment and apical fusion or non-fusion of the costate ornamentation distinguishes two species pairs. These pairs occur on either side of the Pacific basin and include one velate and one non-velate species each: B. longicollis, B. elatus (E Asia) and B. jalapensis, B. singerii (America). Now that discrete morphological entities are clarified and recognizable, phylogenetic hypotheses can be attempted to test these concepts and perhaps infer the monophyly of section Ixocephali when appropriate sequence data are available from newly collected, properly vouchered and viable specimens. Concept Drift (dpeaa)DE-He213 Clamp Connection (dpeaa)DE-He213 Tramal (dpeaa)DE-He213 Unpaved Road (dpeaa)DE-He213 Spore Morphology (dpeaa)DE-He213 Ortiz-Santana, Beatriz aut Enthalten in Mycological progress Berlin : Springer, 2002 8(2009), 3 vom: 16. Apr. (DE-627)509398952 (DE-600)2226747-5 1861-8952 nnns volume:8 year:2009 number:3 day:16 month:04 https://dx.doi.org/10.1007/s11557-009-0595-3 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 8 2009 3 16 04
allfieldsGer	10.1007/s11557-009-0595-3 doi (DE-627)SPR02074546X (SPR)s11557-009-0595-3-e DE-627 ger DE-627 rakwb eng Halling, Roy E. verfasserin aut A revision of Boletellus sect. Ixocephali 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © German Mycological Society and Springer 2009 Abstract Taxa included in Boletellus section Ixocephali sensu Singer are re-evaluated and species limits are clarified in a morphological context. In this revision, we recognize four distinct morphological species: B. jalapensis, B. elatus, B. longicollis, and B. singerii. Among these, we have ascertained that the concept of B. jalapensis was broadened to include another taxon (B. singerii) that was eventually recognized as distinct. Details of spore morphology that include size and shape also show that the precise longitudinal alignment and apical fusion or non-fusion of the costate ornamentation distinguishes two species pairs. These pairs occur on either side of the Pacific basin and include one velate and one non-velate species each: B. longicollis, B. elatus (E Asia) and B. jalapensis, B. singerii (America). Now that discrete morphological entities are clarified and recognizable, phylogenetic hypotheses can be attempted to test these concepts and perhaps infer the monophyly of section Ixocephali when appropriate sequence data are available from newly collected, properly vouchered and viable specimens. Concept Drift (dpeaa)DE-He213 Clamp Connection (dpeaa)DE-He213 Tramal (dpeaa)DE-He213 Unpaved Road (dpeaa)DE-He213 Spore Morphology (dpeaa)DE-He213 Ortiz-Santana, Beatriz aut Enthalten in Mycological progress Berlin : Springer, 2002 8(2009), 3 vom: 16. Apr. (DE-627)509398952 (DE-600)2226747-5 1861-8952 nnns volume:8 year:2009 number:3 day:16 month:04 https://dx.doi.org/10.1007/s11557-009-0595-3 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 8 2009 3 16 04
allfieldsSound	10.1007/s11557-009-0595-3 doi (DE-627)SPR02074546X (SPR)s11557-009-0595-3-e DE-627 ger DE-627 rakwb eng Halling, Roy E. verfasserin aut A revision of Boletellus sect. Ixocephali 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © German Mycological Society and Springer 2009 Abstract Taxa included in Boletellus section Ixocephali sensu Singer are re-evaluated and species limits are clarified in a morphological context. In this revision, we recognize four distinct morphological species: B. jalapensis, B. elatus, B. longicollis, and B. singerii. Among these, we have ascertained that the concept of B. jalapensis was broadened to include another taxon (B. singerii) that was eventually recognized as distinct. Details of spore morphology that include size and shape also show that the precise longitudinal alignment and apical fusion or non-fusion of the costate ornamentation distinguishes two species pairs. These pairs occur on either side of the Pacific basin and include one velate and one non-velate species each: B. longicollis, B. elatus (E Asia) and B. jalapensis, B. singerii (America). Now that discrete morphological entities are clarified and recognizable, phylogenetic hypotheses can be attempted to test these concepts and perhaps infer the monophyly of section Ixocephali when appropriate sequence data are available from newly collected, properly vouchered and viable specimens. Concept Drift (dpeaa)DE-He213 Clamp Connection (dpeaa)DE-He213 Tramal (dpeaa)DE-He213 Unpaved Road (dpeaa)DE-He213 Spore Morphology (dpeaa)DE-He213 Ortiz-Santana, Beatriz aut Enthalten in Mycological progress Berlin : Springer, 2002 8(2009), 3 vom: 16. Apr. (DE-627)509398952 (DE-600)2226747-5 1861-8952 nnns volume:8 year:2009 number:3 day:16 month:04 https://dx.doi.org/10.1007/s11557-009-0595-3 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 8 2009 3 16 04
language	English
source	Enthalten in Mycological progress 8(2009), 3 vom: 16. Apr. volume:8 year:2009 number:3 day:16 month:04
sourceStr	Enthalten in Mycological progress 8(2009), 3 vom: 16. Apr. volume:8 year:2009 number:3 day:16 month:04
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Concept Drift Clamp Connection Tramal Unpaved Road Spore Morphology
isfreeaccess_bool	false
container_title	Mycological progress
authorswithroles_txt_mv	Halling, Roy E. @@aut@@ Ortiz-Santana, Beatriz @@aut@@
publishDateDaySort_date	2009-04-16T00:00:00Z
hierarchy_top_id	509398952
id	SPR02074546X
language_de	englisch
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author	Halling, Roy E.
spellingShingle	Halling, Roy E. misc Concept Drift misc Clamp Connection misc Tramal misc Unpaved Road misc Spore Morphology A revision of Boletellus sect. Ixocephali
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topic_title	A revision of Boletellus sect. Ixocephali Concept Drift (dpeaa)DE-He213 Clamp Connection (dpeaa)DE-He213 Tramal (dpeaa)DE-He213 Unpaved Road (dpeaa)DE-He213 Spore Morphology (dpeaa)DE-He213
topic	misc Concept Drift misc Clamp Connection misc Tramal misc Unpaved Road misc Spore Morphology
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title	A revision of Boletellus sect. Ixocephali
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title_full	A revision of Boletellus sect. Ixocephali
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author_browse	Halling, Roy E. Ortiz-Santana, Beatriz
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doi_str_mv	10.1007/s11557-009-0595-3
title_sort	revision of boletellus sect. ixocephali
title_auth	A revision of Boletellus sect. Ixocephali
abstract	Abstract Taxa included in Boletellus section Ixocephali sensu Singer are re-evaluated and species limits are clarified in a morphological context. In this revision, we recognize four distinct morphological species: B. jalapensis, B. elatus, B. longicollis, and B. singerii. Among these, we have ascertained that the concept of B. jalapensis was broadened to include another taxon (B. singerii) that was eventually recognized as distinct. Details of spore morphology that include size and shape also show that the precise longitudinal alignment and apical fusion or non-fusion of the costate ornamentation distinguishes two species pairs. These pairs occur on either side of the Pacific basin and include one velate and one non-velate species each: B. longicollis, B. elatus (E Asia) and B. jalapensis, B. singerii (America). Now that discrete morphological entities are clarified and recognizable, phylogenetic hypotheses can be attempted to test these concepts and perhaps infer the monophyly of section Ixocephali when appropriate sequence data are available from newly collected, properly vouchered and viable specimens. © German Mycological Society and Springer 2009
abstractGer	Abstract Taxa included in Boletellus section Ixocephali sensu Singer are re-evaluated and species limits are clarified in a morphological context. In this revision, we recognize four distinct morphological species: B. jalapensis, B. elatus, B. longicollis, and B. singerii. Among these, we have ascertained that the concept of B. jalapensis was broadened to include another taxon (B. singerii) that was eventually recognized as distinct. Details of spore morphology that include size and shape also show that the precise longitudinal alignment and apical fusion or non-fusion of the costate ornamentation distinguishes two species pairs. These pairs occur on either side of the Pacific basin and include one velate and one non-velate species each: B. longicollis, B. elatus (E Asia) and B. jalapensis, B. singerii (America). Now that discrete morphological entities are clarified and recognizable, phylogenetic hypotheses can be attempted to test these concepts and perhaps infer the monophyly of section Ixocephali when appropriate sequence data are available from newly collected, properly vouchered and viable specimens. © German Mycological Society and Springer 2009
abstract_unstemmed	Abstract Taxa included in Boletellus section Ixocephali sensu Singer are re-evaluated and species limits are clarified in a morphological context. In this revision, we recognize four distinct morphological species: B. jalapensis, B. elatus, B. longicollis, and B. singerii. Among these, we have ascertained that the concept of B. jalapensis was broadened to include another taxon (B. singerii) that was eventually recognized as distinct. Details of spore morphology that include size and shape also show that the precise longitudinal alignment and apical fusion or non-fusion of the costate ornamentation distinguishes two species pairs. These pairs occur on either side of the Pacific basin and include one velate and one non-velate species each: B. longicollis, B. elatus (E Asia) and B. jalapensis, B. singerii (America). Now that discrete morphological entities are clarified and recognizable, phylogenetic hypotheses can be attempted to test these concepts and perhaps infer the monophyly of section Ixocephali when appropriate sequence data are available from newly collected, properly vouchered and viable specimens. © German Mycological Society and Springer 2009
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container_issue	3
title_short	A revision of Boletellus sect. Ixocephali
url	https://dx.doi.org/10.1007/s11557-009-0595-3
remote_bool	true
author2	Ortiz-Santana, Beatriz
author2Str	Ortiz-Santana, Beatriz
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doi_str	10.1007/s11557-009-0595-3
up_date	2024-07-03T18:00:32.031Z
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score	7.4013834

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A revision of Boletellus sect. Ixocephali

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