Mixed infections of grapevine leaf rusts Phakopsora meliosmae-myrianthae and P. montana in Japan
Abstract Mixed infections of grapevine leaves by the grapevine leaf rust fungi Phakopsora meliosmae-myrianthae and P. montana were assumed because of the frequent sympatric occurrences of the two species in Honshu, Japan. This assumption was proven by experimental basidiospore inoculations of Melios...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Ono, Yoshitaka [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2016 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Journal of general plant pathology - Tokyo : Springer, 2000, 82(2016), 3 vom: 15. März, Seite 149-153 |
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| Übergeordnetes Werk: |
volume:82 ; year:2016 ; number:3 ; day:15 ; month:03 ; pages:149-153 |
| Links: |
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| DOI / URN: |
10.1007/s10327-016-0655-x |
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| Katalog-ID: |
SPR009445811 |
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| 245 | 1 | 0 | |a Mixed infections of grapevine leaf rusts Phakopsora meliosmae-myrianthae and P. montana in Japan |
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| 520 | |a Abstract Mixed infections of grapevine leaves by the grapevine leaf rust fungi Phakopsora meliosmae-myrianthae and P. montana were assumed because of the frequent sympatric occurrences of the two species in Honshu, Japan. This assumption was proven by experimental basidiospore inoculations of Meliosma myriantha and M. tenuis. Basidiospores formed on telial clusters from one rusted grapevine leaf infected both M. myriantha and M. tenuis, resulting in spermogonium and aecium production on the inoculated leaves. However, the aeciospores formed on the two Meliosma species differed; those on M. myriantha were apically thick-walled, characteristic of P. meliosmae-myrianthae, and those on M. tenuis were evenly thin-walled, characteristic of P. montana. | ||
| 650 | 4 | |a Geographic distribution |7 (dpeaa)DE-He213 | |
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| 650 | 4 | |a Taxonomy |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Vitaceae |7 (dpeaa)DE-He213 | |
| 773 | 0 | 8 | |i Enthalten in |t Journal of general plant pathology |d Tokyo : Springer, 2000 |g 82(2016), 3 vom: 15. März, Seite 149-153 |w (DE-627)362771189 |w (DE-600)2100156-X |x 1610-739X |7 nnns |
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10.1007/s10327-016-0655-x doi (DE-627)SPR009445811 (SPR)s10327-016-0655-x-e DE-627 ger DE-627 rakwb eng 630 ASE 580 ASE 48.54 bkl Ono, Yoshitaka verfasserin aut Mixed infections of grapevine leaf rusts Phakopsora meliosmae-myrianthae and P. montana in Japan 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Mixed infections of grapevine leaves by the grapevine leaf rust fungi Phakopsora meliosmae-myrianthae and P. montana were assumed because of the frequent sympatric occurrences of the two species in Honshu, Japan. This assumption was proven by experimental basidiospore inoculations of Meliosma myriantha and M. tenuis. Basidiospores formed on telial clusters from one rusted grapevine leaf infected both M. myriantha and M. tenuis, resulting in spermogonium and aecium production on the inoculated leaves. However, the aeciospores formed on the two Meliosma species differed; those on M. myriantha were apically thick-walled, characteristic of P. meliosmae-myrianthae, and those on M. tenuis were evenly thin-walled, characteristic of P. montana. Geographic distribution (dpeaa)DE-He213 Meliosmaceae (dpeaa)DE-He213 Pucciniales (dpeaa)DE-He213 Taxonomy (dpeaa)DE-He213 Vitaceae (dpeaa)DE-He213 Enthalten in Journal of general plant pathology Tokyo : Springer, 2000 82(2016), 3 vom: 15. März, Seite 149-153 (DE-627)362771189 (DE-600)2100156-X 1610-739X nnns volume:82 year:2016 number:3 day:15 month:03 pages:149-153 https://dx.doi.org/10.1007/s10327-016-0655-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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 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_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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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 48.54 ASE AR 82 2016 3 15 03 149-153 |
| spelling |
10.1007/s10327-016-0655-x doi (DE-627)SPR009445811 (SPR)s10327-016-0655-x-e DE-627 ger DE-627 rakwb eng 630 ASE 580 ASE 48.54 bkl Ono, Yoshitaka verfasserin aut Mixed infections of grapevine leaf rusts Phakopsora meliosmae-myrianthae and P. montana in Japan 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Mixed infections of grapevine leaves by the grapevine leaf rust fungi Phakopsora meliosmae-myrianthae and P. montana were assumed because of the frequent sympatric occurrences of the two species in Honshu, Japan. This assumption was proven by experimental basidiospore inoculations of Meliosma myriantha and M. tenuis. Basidiospores formed on telial clusters from one rusted grapevine leaf infected both M. myriantha and M. tenuis, resulting in spermogonium and aecium production on the inoculated leaves. However, the aeciospores formed on the two Meliosma species differed; those on M. myriantha were apically thick-walled, characteristic of P. meliosmae-myrianthae, and those on M. tenuis were evenly thin-walled, characteristic of P. montana. Geographic distribution (dpeaa)DE-He213 Meliosmaceae (dpeaa)DE-He213 Pucciniales (dpeaa)DE-He213 Taxonomy (dpeaa)DE-He213 Vitaceae (dpeaa)DE-He213 Enthalten in Journal of general plant pathology Tokyo : Springer, 2000 82(2016), 3 vom: 15. März, Seite 149-153 (DE-627)362771189 (DE-600)2100156-X 1610-739X nnns volume:82 year:2016 number:3 day:15 month:03 pages:149-153 https://dx.doi.org/10.1007/s10327-016-0655-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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 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_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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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 48.54 ASE AR 82 2016 3 15 03 149-153 |
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10.1007/s10327-016-0655-x doi (DE-627)SPR009445811 (SPR)s10327-016-0655-x-e DE-627 ger DE-627 rakwb eng 630 ASE 580 ASE 48.54 bkl Ono, Yoshitaka verfasserin aut Mixed infections of grapevine leaf rusts Phakopsora meliosmae-myrianthae and P. montana in Japan 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Mixed infections of grapevine leaves by the grapevine leaf rust fungi Phakopsora meliosmae-myrianthae and P. montana were assumed because of the frequent sympatric occurrences of the two species in Honshu, Japan. This assumption was proven by experimental basidiospore inoculations of Meliosma myriantha and M. tenuis. Basidiospores formed on telial clusters from one rusted grapevine leaf infected both M. myriantha and M. tenuis, resulting in spermogonium and aecium production on the inoculated leaves. However, the aeciospores formed on the two Meliosma species differed; those on M. myriantha were apically thick-walled, characteristic of P. meliosmae-myrianthae, and those on M. tenuis were evenly thin-walled, characteristic of P. montana. Geographic distribution (dpeaa)DE-He213 Meliosmaceae (dpeaa)DE-He213 Pucciniales (dpeaa)DE-He213 Taxonomy (dpeaa)DE-He213 Vitaceae (dpeaa)DE-He213 Enthalten in Journal of general plant pathology Tokyo : Springer, 2000 82(2016), 3 vom: 15. März, Seite 149-153 (DE-627)362771189 (DE-600)2100156-X 1610-739X nnns volume:82 year:2016 number:3 day:15 month:03 pages:149-153 https://dx.doi.org/10.1007/s10327-016-0655-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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 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_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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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 48.54 ASE AR 82 2016 3 15 03 149-153 |
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10.1007/s10327-016-0655-x doi (DE-627)SPR009445811 (SPR)s10327-016-0655-x-e DE-627 ger DE-627 rakwb eng 630 ASE 580 ASE 48.54 bkl Ono, Yoshitaka verfasserin aut Mixed infections of grapevine leaf rusts Phakopsora meliosmae-myrianthae and P. montana in Japan 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Mixed infections of grapevine leaves by the grapevine leaf rust fungi Phakopsora meliosmae-myrianthae and P. montana were assumed because of the frequent sympatric occurrences of the two species in Honshu, Japan. This assumption was proven by experimental basidiospore inoculations of Meliosma myriantha and M. tenuis. Basidiospores formed on telial clusters from one rusted grapevine leaf infected both M. myriantha and M. tenuis, resulting in spermogonium and aecium production on the inoculated leaves. However, the aeciospores formed on the two Meliosma species differed; those on M. myriantha were apically thick-walled, characteristic of P. meliosmae-myrianthae, and those on M. tenuis were evenly thin-walled, characteristic of P. montana. Geographic distribution (dpeaa)DE-He213 Meliosmaceae (dpeaa)DE-He213 Pucciniales (dpeaa)DE-He213 Taxonomy (dpeaa)DE-He213 Vitaceae (dpeaa)DE-He213 Enthalten in Journal of general plant pathology Tokyo : Springer, 2000 82(2016), 3 vom: 15. März, Seite 149-153 (DE-627)362771189 (DE-600)2100156-X 1610-739X nnns volume:82 year:2016 number:3 day:15 month:03 pages:149-153 https://dx.doi.org/10.1007/s10327-016-0655-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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 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_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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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 48.54 ASE AR 82 2016 3 15 03 149-153 |
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10.1007/s10327-016-0655-x doi (DE-627)SPR009445811 (SPR)s10327-016-0655-x-e DE-627 ger DE-627 rakwb eng 630 ASE 580 ASE 48.54 bkl Ono, Yoshitaka verfasserin aut Mixed infections of grapevine leaf rusts Phakopsora meliosmae-myrianthae and P. montana in Japan 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Mixed infections of grapevine leaves by the grapevine leaf rust fungi Phakopsora meliosmae-myrianthae and P. montana were assumed because of the frequent sympatric occurrences of the two species in Honshu, Japan. This assumption was proven by experimental basidiospore inoculations of Meliosma myriantha and M. tenuis. Basidiospores formed on telial clusters from one rusted grapevine leaf infected both M. myriantha and M. tenuis, resulting in spermogonium and aecium production on the inoculated leaves. However, the aeciospores formed on the two Meliosma species differed; those on M. myriantha were apically thick-walled, characteristic of P. meliosmae-myrianthae, and those on M. tenuis were evenly thin-walled, characteristic of P. montana. Geographic distribution (dpeaa)DE-He213 Meliosmaceae (dpeaa)DE-He213 Pucciniales (dpeaa)DE-He213 Taxonomy (dpeaa)DE-He213 Vitaceae (dpeaa)DE-He213 Enthalten in Journal of general plant pathology Tokyo : Springer, 2000 82(2016), 3 vom: 15. März, Seite 149-153 (DE-627)362771189 (DE-600)2100156-X 1610-739X nnns volume:82 year:2016 number:3 day:15 month:03 pages:149-153 https://dx.doi.org/10.1007/s10327-016-0655-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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 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_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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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 48.54 ASE AR 82 2016 3 15 03 149-153 |
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Enthalten in Journal of general plant pathology 82(2016), 3 vom: 15. März, Seite 149-153 volume:82 year:2016 number:3 day:15 month:03 pages:149-153 |
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Geographic distribution Meliosmaceae Pucciniales Taxonomy Vitaceae |
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Journal of general plant pathology |
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Ono, Yoshitaka @@aut@@ |
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| author |
Ono, Yoshitaka |
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Ono, Yoshitaka ddc 630 ddc 580 bkl 48.54 misc Geographic distribution misc Meliosmaceae misc Pucciniales misc Taxonomy misc Vitaceae Mixed infections of grapevine leaf rusts Phakopsora meliosmae-myrianthae and P. montana in Japan |
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630 ASE 580 ASE 48.54 bkl Mixed infections of grapevine leaf rusts Phakopsora meliosmae-myrianthae and P. montana in Japan Geographic distribution (dpeaa)DE-He213 Meliosmaceae (dpeaa)DE-He213 Pucciniales (dpeaa)DE-He213 Taxonomy (dpeaa)DE-He213 Vitaceae (dpeaa)DE-He213 |
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ddc 630 ddc 580 bkl 48.54 misc Geographic distribution misc Meliosmaceae misc Pucciniales misc Taxonomy misc Vitaceae |
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ddc 630 ddc 580 bkl 48.54 misc Geographic distribution misc Meliosmaceae misc Pucciniales misc Taxonomy misc Vitaceae |
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Mixed infections of grapevine leaf rusts Phakopsora meliosmae-myrianthae and P. montana in Japan |
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Mixed infections of grapevine leaf rusts Phakopsora meliosmae-myrianthae and P. montana in Japan |
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Ono, Yoshitaka |
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mixed infections of grapevine leaf rusts phakopsora meliosmae-myrianthae and p. montana in japan |
| title_auth |
Mixed infections of grapevine leaf rusts Phakopsora meliosmae-myrianthae and P. montana in Japan |
| abstract |
Abstract Mixed infections of grapevine leaves by the grapevine leaf rust fungi Phakopsora meliosmae-myrianthae and P. montana were assumed because of the frequent sympatric occurrences of the two species in Honshu, Japan. This assumption was proven by experimental basidiospore inoculations of Meliosma myriantha and M. tenuis. Basidiospores formed on telial clusters from one rusted grapevine leaf infected both M. myriantha and M. tenuis, resulting in spermogonium and aecium production on the inoculated leaves. However, the aeciospores formed on the two Meliosma species differed; those on M. myriantha were apically thick-walled, characteristic of P. meliosmae-myrianthae, and those on M. tenuis were evenly thin-walled, characteristic of P. montana. |
| abstractGer |
Abstract Mixed infections of grapevine leaves by the grapevine leaf rust fungi Phakopsora meliosmae-myrianthae and P. montana were assumed because of the frequent sympatric occurrences of the two species in Honshu, Japan. This assumption was proven by experimental basidiospore inoculations of Meliosma myriantha and M. tenuis. Basidiospores formed on telial clusters from one rusted grapevine leaf infected both M. myriantha and M. tenuis, resulting in spermogonium and aecium production on the inoculated leaves. However, the aeciospores formed on the two Meliosma species differed; those on M. myriantha were apically thick-walled, characteristic of P. meliosmae-myrianthae, and those on M. tenuis were evenly thin-walled, characteristic of P. montana. |
| abstract_unstemmed |
Abstract Mixed infections of grapevine leaves by the grapevine leaf rust fungi Phakopsora meliosmae-myrianthae and P. montana were assumed because of the frequent sympatric occurrences of the two species in Honshu, Japan. This assumption was proven by experimental basidiospore inoculations of Meliosma myriantha and M. tenuis. Basidiospores formed on telial clusters from one rusted grapevine leaf infected both M. myriantha and M. tenuis, resulting in spermogonium and aecium production on the inoculated leaves. However, the aeciospores formed on the two Meliosma species differed; those on M. myriantha were apically thick-walled, characteristic of P. meliosmae-myrianthae, and those on M. tenuis were evenly thin-walled, characteristic of P. montana. |
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| container_issue |
3 |
| title_short |
Mixed infections of grapevine leaf rusts Phakopsora meliosmae-myrianthae and P. montana in Japan |
| url |
https://dx.doi.org/10.1007/s10327-016-0655-x |
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| doi_str |
10.1007/s10327-016-0655-x |
| up_date |
2024-07-04T02:05:49.655Z |
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1803612323484532736 |
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