DOCSLIB.ORG

Konkordanzverzeichnis / Korrigenda Band 2

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Konkordanzverzeichnis / Korrigenda Band 2 A B C D E F G BKH 2 I J K L M N O Gattung Art Autor Familie deutsch Name Essbarkeit BK-Berichtigung Bemerkungen Unt. Abt. Klasse Unt. Gattung Lebensweise Ordnung Synonyme nach neusten nach neusten einer Erkenntnissen zugewiesen Art andern 1 sind Art-Nr. markierte Rot 2 6 Ditiola peziziformis (Lév.) D.A Reid Dacrymycetaceae Gelbweisser Gallertkreisel kein Speisepilz Basidiomycota Dacrymycetes SaprobeDacrymycetales Femsjonia p. nicht pezizaeformis 3 9 Helicobasidium purpureum (Tul.) Bat. Helicobasidiaceae Violette Schneckenbasidie kein Speisepilz Basidiomycota Pucciniomycetes SaprobeHelicobasidiales H. brebissonii 4 13 Sebacina grisea (Bres.) Borudot & Maire Sebacinaceae Graue Wachskruste kein Speisepilz Basidiomycota Agaricomycetes SaprobeSebacinales Exidiopsis g. 5 21 Exidia nigricans (With.) P. Roberts Auriculariaceae Warziger Drüsling, Hexenbutter kein Speisepilz Basidiomycota Agaricomycetes SaprobeAuriculariales E. plana, E. glandulosa Fr., E. pithya 6 22 Exidia nigricans (With.) P. Roberts Auriculariaceae Warziger Drüsling, Hexenbutter kein Speisepilz Basidiomycota Agaricomycetes SaprobeAuriculariales E. plana, E. glandulosa Fr., E. pithya 7 25 Exidia glandulosa Bull. Auriculariaceae Stoppeliger Becher-Drüsling kein Speisepilz Basidiomycota Agaricomycetes SaprobeAuriculariales E. truncata 8 28 Tremella globispora D.A. Reid Tremellaceae Buckeliger Rundspor-Zitterling kein Speisepilz Basidiomycota Tremellomycetes SaprobeTremellales nicht T. globospora 9 30 Phaeotremella simplex (H.S. Jacks & G.W. Martin) MillanesTremellaceae & Wedin Breitsporiger Mehlscheibenzitterling kein Speisepilz Basidiomycota Tremellomycetes ParasitTremellales Tremella s. 10 31 Guepinia helvelloides (DC.) Fr. Incertae sedis Fleischroter Gallerttrichter Speisepilz Basidiomycota Agaricomycetes SaprobeAuriculariales Tremiscus h. 11 32 Tulasnella pallida (Johan-Olsen) Juel (1897) Tulasnellaceae Blassvioletter Wachskrustenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeCantharellales T. violacea 12 41 Rhizoctonia pseudocornigera (M.P. Christ) Oberw., R. Bauer,Ceratobasidiaceae Garnica & R. KirschnerFastgehörnte Hydrabasidie kein Speisepilz Basidiomycota Agaricomycetes SaprobeCantharellales Ceratobasidium p. 13 42 Rhizoctonia fusispora (J. Schröt.) Oberw., R. Bauer, GarnicaCeratobasidiaceae & R. Kirschner Spindelsporige Hydrabasidie kein Speisepilz Basidiomycota Agaricomycetes SaprobeCantharellales Hypochnus fusisporus, Thanatephorus f. 14 44 Rhizoctonia ochracea (Massee) Oberw., R. Bauer, GarnicaCeratobasidiaceae & R. Kirschner Ockerfarbene Hydrabasidie kein Speisepilz Basidiomycota Agaricomycetes SaprobeCantharellales Uthatobasidium o. 15 48 Athelopsis lacerata (Litsch.) Hjortst. & Ryv. Atheliaceae Rissige Scheingewebehaut kein Speisepilz Basidiomycota Agaricomycetes SaprobeAtheliales Amylocorticium l. 16 55 Eonema pyriforme (M.P. Christ.) Redhead, Lücking & LawreyHygrophoraceae Birnensporige Fadenhaut kein Speisepilz Basidiomycota Agaricomycetes Agaricales Athelia p. 17 56 Scytinostromella olivaceoalba (Bourdot & GalzinI) Ginns & M.N.L.Incertae Lefebvre sedis Olivweisser Scheinlederrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeRussulales Confertobasidium o. 18 58 Leptosporomyces septentrionalis (J. Erikss.) L.G. Krieglst. Atheliaceae Nordischer Watteschwamm kein Speisepilz Basidiomycota Agaricomycetes SaprobeAtheliales Fibulomyces s. 19 61 Botryobasidium vagum (Curtis & Berk.) Rogers 1935 Botryobasidiaceae Schiffchensporige Traubenbasidie kein Speisepilz Basidiomycota Agaricomycetes SaprobeCantharellales B. botryosum 20 68 Botryobasidium conspersum J. Erikss. Botryobasidiaceae Zerstreute Traubenbasidie kein Speisepilz Basidiomycota Agaricomycetes SaprobeCantharellales Haplotrichum c. 21 70 Byssocorticium efibulatum Hjortstam & Ryvarden Atheliaceae Schnallenloser Filzrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeAtheliales nicht B. pulchrum 22 71 Veluticeps abietina (Pers.) Hjortstam & Telleria Gloeophyllaceae Graublauer Samtzystidenschichtpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeGloeophyllales Columnocystis a. 23 72 Veluticeps ambigua (Peck) Hjortstam & TellerÌa Gloeophyllaceae Brauner Samtzystidenschichtpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeGloeophyllales Columnocystis a. 24 74 Vuilleminia macrospora (Bres.) Hjortstam Corticiaceae Grosssporiger Rindensprenger kein Speisepilz Basidiomycota Agaricomycetes SaprobeCorticiales Corticium macrosporopsis 25 76 Hyphodontia alutaria (Burt) J. Erikss. Schizoporaceae Ledergelber Zähnchenrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeHymenochaetales Grandinia a. 26 77 Hyphodontia arguta (Fr.) J. Erikss. Schizoporaceae Spitzstachliger Zähnchen-Rindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeHymenochaetales Grandinia a. 27 78 Hyphodontia barba-jovis (Bull.) J. Erikss. Schizoporaceae Bärtiger Zähnchenrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeHymenochaetales Grandinia b. 28 79 Xylodon brevisetus (P. Karst.) Hjorststam & RyvardenSchizoporaceae Kurzstacheliger Holzzähnchenrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeHymenochaetales Grandinia b. 29 80 Hyphodontia cineracea (Bourdot & Galzin) J. Erikss. & HjortstamSchizoporaceae Aschgrauer Zähnchenrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeHymenochaetales Grandinia c. 30 81 Basidioradulum crustosum (Pers.) Zmitr., Malysheva & SpirinSchizoporaceae Krustiger Reibeisenrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeHymenochaetales Grandinia c. 31 82 Xylodon asperus (Fr.) Hjortstam & Ryvarden Schizoporaceae Rauer Holzzähnchenrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeHymenochaetales Grandinia a. nicht Grandinia granulosa 32 83 Xylodon nespori (Bres.) Hjortstam & Ryvarden Schizoporaceae Warziger Holzzähnchenrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeHymenochaetales Grandinia n. 33 84 Hyphodontia pallidula (Bres.) J. Erikss. Schizoporaceae Blasser Zähnchenrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeHymenochaetales Grandinia p. 34 85 Alutaceodontia alutacea (Fr.) Hjortstam & Ryvarden Schizoporaceea Schmalsporiger Lederzähnchenrindenpilz kein Speisepilz Basidiomycota Agaricomycetes Hymenochaetales Grandinia stenospora 35 86 Hyphodontia subalutacea (P. Karst.) J. Erikss. Schizoporaceae Langzystiden-Zähnchenrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeHymenochaetales Grandinia s. 36 87 Terana caerulea (Lam.) Kuntze Phanerochaetaceae Indigo-Farbrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobePolyporales Pulcherricium c. 37 88 Cristinia eichleri (Pers.) Nakasone Stephanosporaceae Raspelförmiger Körnchenrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeRussulaes C. gallica 38 92 Cylindrobasidium laeve (Pers.) Chamuris Physalacriaceae Ablösender Rindenschwamm kein Speisepilz Basidiomycota Agaricomycetes SaprobeAgaricales C. evolvens nach IF ≠ C. evolvens 39 93 Radulomyces confluens (Fr.) M.P. Christ Pterulaceae Zusammenfliessender Reibeisenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeAgaricales Cerocorticium c. 40 94 Radulomyces molaris (Chaillet ex Fr.) M.P. Christ Pterulaceae Gezähnelter Reibeisenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeAgaricales Cerocorticium m. 41 96 Cystostereum murrayi (Berk. & M.A. Curtis) Pouzar Cystostereaceae Subalpiner Duftschichtpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobePolyporales Schreibweise: nicht murraii 42 100 Scytinostroma hemidichophyticum Pouzar Lachnocladiaceae Rundlichsporiger Lederrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeRussulales nicht S. portentosum S. portentosum ist Art aus N-Amerika 43 101 Amylocorticiellum molle (Fr.) Spirin & Zmitr. Amylocorticiaceae Weiche Amylowattehaut kein Speisepilz Basidiomycota Agaricomycetes SaprobeAmylocorticiales Hypochniciellum m. 44 104 Gloeocystidiellum luridum (Bres.) Boidin Stereaceae Auenwald-Saftzystidling kein Speisepilz Basidiomycota Agaricomycetes SaprobeRussulales Megalocystidium l. 45 107 Gloiothele lactescens (Berk.) Hjortstam Peniophoraceae Milchender Rindenzystidling kein Speisepilz Basidiomycota Agaricomycetes SaprobeRussulales Megalocystidium l. 46 108 Gloeocystidiellum leucoxanthum (Bres.) Boidin Stereaceae Gelbweisser Saftzystidling kein Speisepilz Basidiomycota Agaricomycetes Russulales Megalocystidium l. 47 109 Gloiothele citrina (Pers.) Ginns & G.W. Freeman Peniophoraceae Zitronengelber Rindenzystidling kein Speisepilz Basidiomycota Agaricomycetes SaprobeRussulales Vesiculomyces c. 48 110 Phlebiella christiansenii (Parmasto) K.H. Larss. & HjortstamIncertae sedis Honiggelbe Faserrandwachshaut kein Speisepilz Basidiomycota Agaricomycetes SaprobePolyporales Trechispora c. 49 115 Trechispora hymenocystis (Berk. & Broome) K.H. Larss. Hydnodontaceae Schneeweisser Zysten-Stachelsporrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeTrechisporales nicht T. mollusca 50 117 Xenasmatella vaga (Fr.) Stalpers Xenasmataceae Schwefelgelbe Warzensporwachshaut kein Speisepilz Basidiomycota Agaricomycetes SaprobePolyporales Phlebiella vaga, Trechispora vaga 51 123 Kurtia argillacea (Bres.) Karasiński Corticiaceae Tonfarbener Flaumrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeCorticiales Hyphoderma a. 52 124 Lawrynomyces capitatus (J. Erikss. & Å Strid) KarasińskiIncertae sedis Schnallenloser Kopfzystidenrindenpilz kein Speisepilz Basidiomycota Agaricomycetes SaprobeHymenochaetales Hyhoderma c. 53 125 Mutatoderma mutatum (Peck)
Load more

Recommended publications
  • A New Species of Bondarzewia from India
    Turkish Journal of Botany Turk J Bot (2015) 39: 128-133 http://journals.tubitak.gov.tr/botany/ © TÜBİTAK Research Article doi:10.3906/bot-1402-82 A new species of Bondarzewia from India 1, 1 2 Kanad DAS *, Arvind PARIHAR , Manoj Emanuel HEMBROM 1 Botanical Survey of India, Cryptogamic Unit, P. O. B. Garden, Howrah, India 2 Botanical Survey of India, Central National Herbarium, P. O. B. Garden, Howrah, India Received: 25.02.2014 Accepted: 18.07.2014 Published Online: 02.01.2015 Printed: 30.01.2015 Abstract: Bondarzewia zonata, collected from North Sikkim, is proposed here as new to science. It is characterized by basidiomata with strong zonate pilei, thin context turning persistent dark red with guaiacol, comparatively small spores with narrow ornamented ridges, and an absence of cystidioles. A detailed description coupled with macro- and micromorphological illustrations of this species is provided. Its relation to the allied species is discussed and a provisional key to the species of Bondarzewia is given. Key words: Macrofungi, Bondarzewia, Russulales, new species, taxonomy, Sikkim 1. Introduction Picea. After thorough macro- and micromorphological The genusBondarzewia was first described by Singer studies followed by a survey of the literature, it proved to (1940). Presently, it accommodates subtropical (Dai et be new to science. It is proposed as Bondarzewia zonata al., 2010) to temperate and wood-inhabiting parasitic and described here in detail with illustrations. Its relation (causing white rot) poroid macrofungi. Therefore, the with closely related taxa is also discussed. genus Bondarzewia can be characterized as pileate stipitate to substipitate basidiocarps, with a dimitic hyphal system 2.
    [Show full text]
  • Biodiversity of Wood-Decay Fungi in Italy
    AperTO - Archivio Istituzionale Open Access dell'Università di Torino Biodiversity of wood-decay fungi in Italy This is the author's manuscript Original Citation: Availability: This version is available http://hdl.handle.net/2318/88396 since 2016-10-06T16:54:39Z Published version: DOI:10.1080/11263504.2011.633114 Terms of use: Open Access Anyone can freely access the full text of works made available as "Open Access". Works made available under a Creative Commons license can be used according to the terms and conditions of said license. Use of all other works requires consent of the right holder (author or publisher) if not exempted from copyright protection by the applicable law. (Article begins on next page) 28 September 2021 This is the author's final version of the contribution published as: A. Saitta; A. Bernicchia; S.P. Gorjón; E. Altobelli; V.M. Granito; C. Losi; D. Lunghini; O. Maggi; G. Medardi; F. Padovan; L. Pecoraro; A. Vizzini; A.M. Persiani. Biodiversity of wood-decay fungi in Italy. PLANT BIOSYSTEMS. 145(4) pp: 958-968. DOI: 10.1080/11263504.2011.633114 The publisher's version is available at: http://www.tandfonline.com/doi/abs/10.1080/11263504.2011.633114 When citing, please refer to the published version. Link to this full text: http://hdl.handle.net/2318/88396 This full text was downloaded from iris - AperTO: https://iris.unito.it/ iris - AperTO University of Turin’s Institutional Research Information System and Open Access Institutional Repository Biodiversity of wood-decay fungi in Italy A. Saitta , A. Bernicchia , S. P. Gorjón , E.
    [Show full text]
  • Polypore Diversity in North America with an Annotated Checklist
    Mycol Progress (2016) 15:771–790 DOI 10.1007/s11557-016-1207-7 ORIGINAL ARTICLE Polypore diversity in North America with an annotated checklist Li-Wei Zhou1 & Karen K. Nakasone2 & Harold H. Burdsall Jr.2 & James Ginns3 & Josef Vlasák4 & Otto Miettinen5 & Viacheslav Spirin5 & Tuomo Niemelä 5 & Hai-Sheng Yuan1 & Shuang-Hui He6 & Bao-Kai Cui6 & Jia-Hui Xing6 & Yu-Cheng Dai6 Received: 20 May 2016 /Accepted: 9 June 2016 /Published online: 30 June 2016 # German Mycological Society and Springer-Verlag Berlin Heidelberg 2016 Abstract Profound changes to the taxonomy and classifica- 11 orders, while six other species from three genera have tion of polypores have occurred since the advent of molecular uncertain taxonomic position at the order level. Three orders, phylogenetics in the 1990s. The last major monograph of viz. Polyporales, Hymenochaetales and Russulales, accom- North American polypores was published by Gilbertson and modate most of polypore species (93.7 %) and genera Ryvarden in 1986–1987. In the intervening 30 years, new (88.8 %). We hope that this updated checklist will inspire species, new combinations, and new records of polypores future studies in the polypore mycota of North America and were reported from North America. As a result, an updated contribute to the diversity and systematics of polypores checklist of North American polypores is needed to reflect the worldwide. polypore diversity in there. We recognize 492 species of polypores from 146 genera in North America. Of these, 232 Keywords Basidiomycota . Phylogeny . Taxonomy . species are unchanged from Gilbertson and Ryvarden’smono- Wood-decaying fungus graph, and 175 species required name or authority changes.
    [Show full text]
  • Prospecting Russula Senecis: a Delicacy Among the Tribes of West Bengal
    Prospecting Russula senecis: a delicacy among the tribes of West Bengal Somanjana Khatua, Arun Kumar Dutta and Krishnendu Acharya Molecular and Applied Mycology and Plant Pathology Laboratory, Department of Botany, University of Calcutta, Kolkata, West Bengal, India ABSTRACT Russula senecis, a worldwide distributed mushroom, is exclusively popular among the tribal communities of West Bengal for food purposes. The present study focuses on its reliable taxonomic identification through macro- and micro-morphological features, DNA barcoding, confirmation of its systematic placement by phylogenetic analyses, myco-chemicals and functional activities. For the first time, the complete Internal Transcribed Spacer region of R. senecis has been sequenced and its taxo- nomic position within subsection Foetentinae under series Ingratae of the subgen. Ingratula is confirmed through phylogenetic analysis. For exploration of its medic- inal properties, dried basidiocarps were subjected for preparation of a heat stable phenol rich extract (RusePre) using water and ethanol as solvent system. The an- tioxidant activity was evaluated through hydroxyl radical scavenging (EC50 5 µg/ml), chelating ability of ferrous ion (EC50 0.158 mg/ml), DPPH radical scavenging (EC50 1.34 mg/ml), reducing power (EC50 2.495 mg/ml) and total antioxidant activity methods (13.44 µg ascorbic acid equivalent/mg of extract). RusePre exhibited an- timicrobial potentiality against Listeria monocytogenes, Bacillus subtilis, Pseudomonas aeruginosa and Staphylococcus aureus. Furthermore, diVerent parameters were tested to investigate its chemical composition, which revealed the presence of appreciable quantity of phenolic compounds, along with carotenoids and ascorbic acid. HPLC- UV fingerprint indicated the probable existence of at least 13 phenolics, of which 10 were identified (pyrogallol > kaempferol > quercetin > chlorogenic acid > ferulic Submitted 29 November 2014 acid, cinnamic acid > vanillic acid > salicylic acid > p-coumaric acid > gallic acid).
    [Show full text]
  • Notes, Outline and Divergence Times of Basidiomycota
    Fungal Diversity (2019) 99:105–367 https://doi.org/10.1007/s13225-019-00435-4 (0123456789().,-volV)(0123456789().,- volV) Notes, outline and divergence times of Basidiomycota 1,2,3 1,4 3 5 5 Mao-Qiang He • Rui-Lin Zhao • Kevin D. Hyde • Dominik Begerow • Martin Kemler • 6 7 8,9 10 11 Andrey Yurkov • Eric H. C. McKenzie • Olivier Raspe´ • Makoto Kakishima • Santiago Sa´nchez-Ramı´rez • 12 13 14 15 16 Else C. Vellinga • Roy Halling • Viktor Papp • Ivan V. Zmitrovich • Bart Buyck • 8,9 3 17 18 1 Damien Ertz • Nalin N. Wijayawardene • Bao-Kai Cui • Nathan Schoutteten • Xin-Zhan Liu • 19 1 1,3 1 1 1 Tai-Hui Li • Yi-Jian Yao • Xin-Yu Zhu • An-Qi Liu • Guo-Jie Li • Ming-Zhe Zhang • 1 1 20 21,22 23 Zhi-Lin Ling • Bin Cao • Vladimı´r Antonı´n • Teun Boekhout • Bianca Denise Barbosa da Silva • 18 24 25 26 27 Eske De Crop • Cony Decock • Ba´lint Dima • Arun Kumar Dutta • Jack W. Fell • 28 29 30 31 Jo´ zsef Geml • Masoomeh Ghobad-Nejhad • Admir J. Giachini • Tatiana B. Gibertoni • 32 33,34 17 35 Sergio P. Gorjo´ n • Danny Haelewaters • Shuang-Hui He • Brendan P. Hodkinson • 36 37 38 39 40,41 Egon Horak • Tamotsu Hoshino • Alfredo Justo • Young Woon Lim • Nelson Menolli Jr. • 42 43,44 45 46 47 Armin Mesˇic´ • Jean-Marc Moncalvo • Gregory M. Mueller • La´szlo´ G. Nagy • R. Henrik Nilsson • 48 48 49 2 Machiel Noordeloos • Jorinde Nuytinck • Takamichi Orihara • Cheewangkoon Ratchadawan • 50,51 52 53 Mario Rajchenberg • Alexandre G.
    [Show full text]
  • An Annotated Catalogue of the Fungal Biota of the Roztocze Upland Monika KOZŁOWSKA, Wiesław MUŁENKO Marcin ANUSIEWICZ, Magda MAMCZARZ
    An Annotated Catalogue of the Fungal Biota of the Roztocze Upland Fungal Biota of the An Annotated Catalogue of the Monika KOZŁOWSKA, Wiesław MUŁENKO Marcin ANUSIEWICZ, Magda MAMCZARZ An Annotated Catalogue of the Fungal Biota of the Roztocze Upland Richness, Diversity and Distribution MARIA CURIE-SkłODOWSKA UNIVERSITY PRESS POLISH BOTANICAL SOCIETY Grzyby_okladka.indd 6 11.02.2019 14:52:24 An Annotated Catalogue of the Fungal Biota of the Roztocze Upland Richness, Diversity and Distribution Monika KOZŁOWSKA, Wiesław MUŁENKO Marcin ANUSIEWICZ, Magda MAMCZARZ An Annotated Catalogue of the Fungal Biota of the Roztocze Upland Richness, Diversity and Distribution MARIA CURIE-SkłODOWSKA UNIVERSITY PRESS POLISH BOTANICAL SOCIETY LUBLIN 2019 REVIEWER Dr hab. Małgorzata Ruszkiewicz-Michalska COVER DESIN, TYPESETTING Studio Format © Te Authors, 2019 © Maria Curie-Skłodowska University Press, Lublin 2019 ISBN 978-83-227-9164-6 ISBN 978-83-950171-8-6 ISBN 978-83-950171-9-3 (online) PUBLISHER Polish Botanical Society Al. Ujazdowskie 4, 00-478 Warsaw, Poland pbsociety.org.pl Maria Curie-Skłodowska University Press 20-031 Lublin, ul. Idziego Radziszewskiego 11 tel. (81) 537 53 04 wydawnictwo.umcs.eu [email protected] Sales Department tel. / fax (81) 537 53 02 Internet bookshop: wydawnictwo.umcs.eu [email protected] PRINTED IN POLAND, by „Elpil”, ul. Artyleryjska 11, 08-110 Siedlce AUTHOR’S AFFILIATION Department of Botany and Mycology, Maria Curie-Skłodowska University, Lublin Monika Kozłowska, [email protected]; Wiesław
    [Show full text]
  • Interesting Collections of Polypores in the Czech Republic, Particularly in Moravia – I
    ISSN 1211-8788 Acta Musei Moraviae, Scientiae biologicae (Brno) 102(1): 49–87, 2017 Interesting collections of polypores in the Czech Republic, particularly in Moravia – I 1 2 DANIEL DVOØÁK & JAN BÌŤÁK 1 Dept. of Botany and Zoology, Faculty of Science, Masaryk University, Kotláøská 267/2, CZ-611 37 Brno, Czech Republic; e-mail: [email protected] 2 Dept. of Forest Ecology, The Silva Tarouca Research Institute, Lidická 25/27, CZ-602 00 Brno, Czech Republic; e-mail: [email protected] DVOØÁK D. & BÌŤÁK J. 2017: Interesting collections of polypores in the Czech Republic, particularly in Moravia – I. Acta Musei Moraviae, Scientiae biologicae (Brno) 102(1): 49–87. – An annotated list of some remarkable collections of rare polypores, mainly from the territory of Moravia, is given. Altogether, 36 species are presented, most of them illlustrated with a colour photograph. Some information on their distribution, ecology and key characters is provided. New localities of species previously known merely from only one (Aurantiporus alborubescens, Chaetoporellus latitans, Riopa metamorphosa) or two (Jahnoporus hirtus) in Czechia were disclosed, and a few species (Byssoporia terrestris, Phellinus lundellii) are published for the first time for the territory of Moravia. Further, many new localities for certain other very rare polypores (Gelatoporia subvermispora, Porotheleum fimbriatum, Tyromyces kmetii, Yuchengia narymica) are presented. Key words. Moravia, rare polypores, new records Introduction Polyporoid fungi (or Polyporales s.l.) are among the best-explored groups of macromycetes in Czechia, thanks to the many prominent mycologists who have addressed this group in the past (A. Pilát, F. Kotlaba, Z. Pouzar, A.
    [Show full text]
  • An Overview of Aphyllophorales (Wood Rotting Fungi) from India
    Int.J.Curr.Microbiol.App.Sci (2013) 2(12): 112-139 ISSN: 2319-7706 Volume 2 Number 12 (2013) pp. 112-139 http://www.ijcmas.com Review Article An overview of Aphyllophorales (wood rotting fungi) from India Kiran Ramchandra Ranadive* Waghire College, Saswad, Tal-Purandar, Dist. Pune, Maharashtra (India) *Corresponding author A B S T R A C T K e y w o r d s During field and literature surveys, a rich mycobiota was observed in the vegetation of India. The heavy rainfall and high humidity favours the growth of Fungi; Aphyllophoraceous fungi. The present work materially adds to our knowledge of Aphyllophorales; Poroid and Non-Poroid Aphyllophorales from all over India. A total of more than Basidiomycetes; 190 genera of 52 families and total 1175 species of from poroid and non-poroid semi-evergreen Aphyllophorales fungi were reported from Indian literature till 2012.The checklist gives the total count of aphyllophoraceous fungal diversity from India which is also forest.. a valued addition for comparing aphyllophoraceous diversity in the world. Introduction Aphyllophorales order was proposed by in culture are recognized by Stalper. Rea, after Patouillard, for Basidiomycetes (Stalper,1978). having macroscopic basidiocarps in which the hymenophore is flattened Much of the literature of the order is based (Thelephoraceae), club-like on the traditional family groupings and as (Clavariaceae), tooth-like (Hydnaceae) or under the current re-arrangements, one has the hymenium lining tubes family may exhibit several different types (Polyporaceae) or some times on lamellae, of hymenophore (e.g. Gomphaceae has the poroid or lamellate hymenophores effuse, clavarioid, hydnoid and being tough and not fleshy as in the cantharelloid hymenophores).
    [Show full text]
  • Genera of Corticioid Fungi: Keys, Nomenclature and Taxonomy Article
    Studies in Fungi 5(1): 125–309 (2020) www.studiesinfungi.org ISSN 2465-4973 Article Doi 10.5943/sif/5/1/12 Genera of corticioid fungi: keys, nomenclature and taxonomy Gorjón SP BIOCONS – Department of Botany and Plant Physiology, University of Salamanca, 37007 Salamanca, Spain Gorjón SP 2020 – Genera of corticioid fungi: keys, nomenclature, and taxonomy. Studies in Fungi 5(1), 125–309, Doi 10.5943/sif/5/1/12 Abstract A review of the worldwide corticioid homobasidiomycetes genera is presented. A total of 620 genera are considered with comments on their taxonomy and nomenclature. Of them, about 420 are accepted and keyed out, described in detail with remarks on their taxonomy and systematics. Key words – Corticiaceae – Crust fungi – Diversity – Homobasidiomycetes Introduction Corticioid fungi are a diverse and heterogeneous group of fungi mainly referred to basidiomycete fungi in which basidiomes are generally resupinate. Basidiome construction is often simple, and in most cases, only generative hyphae are found. In more structured basidiomes, those with a reflexed margin or with a pileate surface, more or less sclerified hyphae are usually found. Even the basidiome structure is apparently not very complex, hymenophore configuration should be highly variable finding smooth surfaces or different variations to increase the spore production area such as rugose, tuberculate, aculeate, merulioid, folded, or poroid hymenial surfaces. It is often thought that corticioid fungi produce unattractive and little variable forms and, in most cases, they go unnoticed by most mycologists as ungraceful forms that ‘cover sticks and look like a paint stain’. Although the macroscopic variability compared to other fungi is, but not always, usually limited, under the microscope they surprise with a great diversity of forms of basidia, cystidia, spores and other microscopic elements (Hjortstam et al.
    [Show full text]
  • Podofomes Trogii
    Podofomes trogii Pilzportrait Fungi, Dikarya, Basidiomycota, Agaricomycotina, Agaricomycetes, Polyporales, Polyporaceae, Podofomes Podofomes trogii Gestielter Tannen-Harzporling Podofomes trogii Podofomes trogii (Fries) Pouzar 1971 Polyporus rugosus Trog 1839 Polyporus trogii Fries 1851 Trametes butignotii Boudier ex Lloyd 1910 Pelloporus trogii (Fries) Kotlaba & Pouzar 1957 Podofomes trogii (Fries) Pouzar 1971 Ischnoderma trogii (Fries) Donk 1971 Lasiochlaena trogii (Fries) Krieglsteiner 1991 Dieser seltene Porling wächst an Wurzeln oder Strünken von Abies. Varia Bemerkungen / Hinweise / Abstract Die monotypische Gattung Podofomes mit der Art Podofomes trogii ist ein stipitater Polypore mit einjährigen, nierenförmigen bis infundibuliformen Pilei mit schwarzer Kruste, konzentrisch zonierten, unregelmäßig deklinierten Poren, einem trimitischen Hyphen-System, geklammerten generativen Hyphen, dem Fehlen zystidialer Elemente und ellipsoiden, glatten, in Melzer's Reagenz nicht reagierenden Basidiosporen. Es handelt sich um eine seltene Art, die speziell auf Wurzeln von Abies spp. wächst, eine Weißfäule verursacht und in Mittel- und Südeuropa sowie im Kaukasus verbreitet ist. Bislang sind die phylogenetischen Beziehungen unbekannt, und die Art wurde aufgrund der Morphologie mit der Polypengattung Ischnoderma in Verbindung gebracht. Die vorliegende Phylogenie, basierend auf IST-Analysen, stellt Podofomes trogii unter andere Datronia- Arten und in die Nähe des Gattungstyps Datronia mollis. Wir liefern eine vollständige Beschreibung der Art mit
    [Show full text]
  • Mycotaxon, Ltd
    ISSN (print) 0093-4666 © 2012. Mycotaxon, Ltd. ISSN (online) 2154-8889 MYCOTAXON http://dx.doi.org/10.5248/120.49 Volume 120, pp. 49–58 April–June 2012 Russula jilinensis sp. nov. (Russulaceae) from northeast China Guo-jie Li1, 2, Sai-Fei Li 1, Xing-Zhong Liu1 & Hua-An Wen 1* 1State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, No3 1st West Beichen Road, Chaoyang District, Beijing 100101, China 2Graduate University of Chinese Academy of Sciences, Beijing 100049, China * Correspondence to: [email protected] Abstract — Russula jilinensis (subg. Coccinula sect. Laetinae), is described from Changbai Mountains, northeast China. The new species isdistinguish ed by its bright red glabrous pileus with a cinnamon tinged disc, slightly yellowish context, dark yellow to ocher spore print, and pileipellis with septate pileocystidia. The morphological characteristics are illustrated in detail and compared with those of similar species. Identification of R. jilinensis was supported by the molecular phylogenetic analysis based on the ribosomal DNA internal transcribed spacer regions (ITS). Key words —Russulales, taxonomy, morphology, Basidiomycota Introduction Northeast China, including Liaoning, Jilin, and Heilongjiang Provinces and the eastern part of Inner Mongolia Autonomous Region, covers an area of 1.236×106 km2 (39°–53°30ʹ N 115°–135°E) within the temperate to boreal continental climate zones. Plant communities range from grassland (eastern Inner Mongolia) to broadleaf forest (southern Liaoning), while the three main mountain systems (Great Hinggan, Lesser Hinggan, Changbai) are mostly covered by coniferous or mixed coniferous–broadleaf forests. The main trees in northeast China are Pinus pumila, P. koraiensis, Larix gmelinii, Betula platyphylla, Abies nephrolepis, Picea jezoensis, and Quercus mongolica (Jiang et al.
    [Show full text]
  • Mycological Notes 9: Bondarzewia – a Work in Progress
    Mycological Notes 9: Bondarzewia – a work in progress Jerry Cooper, June 2012 [updated Oct. 2012] I’m not really a bracket person but you can’t ignore a Bondarzewia when you find one, they are big and colourful. Back in 2009 Paul Kirk, an ex-colleague of mine from (what used to be) the International Mycological Institute, was staying with me for a meeting. For a break I took him to one of my favourite collecting localities, a remnant of beech forest at the Hinewai reserve near Akaroa. Paul spotted the big yellow bracket fungus at the base of a red beech. At first I thought it was Laetiporus sulphureus (chicken on the woods) and certainly not something I’d seen before in New Zealand. On cutting the fruitbody it started to exude white latex like a Lactarius, so I was puzzled. Looking at material under the microscope it looked even more like a Lactarius because the spores were amyloid and ornamented, just like Russula and Lactarius. It didn’t take long to track it down as ‘Bondarzewia berkeleyi’, in the order Russulales, and recorded from Japan, Papua New Guinea, Solomon Islands, East North America and China. These days when I see such a broad natural distribution I am immediately suspicious. Increasingly we see molecular data indicating biogeographical and taxonomic complexity; what we considered to be one species if often a number of similar species with more regionalised distribution and interesting biogeographical histories. The commonly recorded species in the northern hemisphere are B. berkeleyi and B. mesenterica (syn. B. montana).
    [Show full text]