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An Annotated Checklist of Volvariella in the Iberian Peninsula and Balearic Islands
Post date: June 2010 Summary published in MYCOTAXON 112: 271–273 An annotated checklist of Volvariella in the Iberian Peninsula and Balearic Islands ALFREDO JUSTO1* & MARÍA LUISA CASTRO2 *[email protected] or [email protected] 1 Biology Department, Clark University. 950 Main St. Worcester, MA 01610 USA 2 Facultade de Bioloxía, Universidade de Vigo. Campus As Lagoas-Marcosende Vigo, 36310 Spain Abstract — Species of Volvariella reported from the Iberian Peninsula (Spain, Portugal) and Balearic Islands (Spain) are listed, with data on their distribution, ecology and phenology. For each taxon a list of all collections examined and a map of its distribution is given. According to our revision 12 taxa of Volvariella occur in the area. Key words — Agaricales, Agaricomycetes, Basidiomycota, biodiverstity, Pluteaceae Introduction Volvariella Speg. is a genus traditionally classified in the family Pluteaceae Kotl. & Pouzar (Agaricales, Basidiomycota), but recent molecular research has challenged its monophyly and taxonomic position within the Agaricales (Moncalvo et al. 2002, Matheny et al. 2006). Its main characteristics are the pluteoid basidiomes (i.e. free lamellae; context of pileus and stipe discontinuous), universal veil present in mature specimens as a saccate volva at stipe base, brownish-pink spores in mass and mainly the inverse lamellar trama. It comprises about 50 species (Kirk et al. 2008) and is widely distributed around the world (Singer 1986). Monographic studies of the genus have been mostly carried out in Europe (Kühner & Romagnesi 1956, Orton 1974, 1986; Boekhout 1990) North America (Shaffer 1957) and Africa (Heinemann 1975, Pegler 1977). In the Iberian Peninsula (Spain, Portugal) and Balearic Islands (Spain) the records of Volvariella are scattered, as they are often included in general checklists and prior to our study the only taxonomic paper on this genus, in this area, was an article by Vila et al. -
Forest Fungi in Ireland
FOREST FUNGI IN IRELAND PAUL DOWDING and LOUIS SMITH COFORD, National Council for Forest Research and Development Arena House Arena Road Sandyford Dublin 18 Ireland Tel: + 353 1 2130725 Fax: + 353 1 2130611 © COFORD 2008 First published in 2008 by COFORD, National Council for Forest Research and Development, Dublin, Ireland. All rights reserved. No part of this publication may be reproduced, or stored in a retrieval system or transmitted in any form or by any means, electronic, electrostatic, magnetic tape, mechanical, photocopying recording or otherwise, without prior permission in writing from COFORD. All photographs and illustrations are the copyright of the authors unless otherwise indicated. ISBN 1 902696 62 X Title: Forest fungi in Ireland. Authors: Paul Dowding and Louis Smith Citation: Dowding, P. and Smith, L. 2008. Forest fungi in Ireland. COFORD, Dublin. The views and opinions expressed in this publication belong to the authors alone and do not necessarily reflect those of COFORD. i CONTENTS Foreword..................................................................................................................v Réamhfhocal...........................................................................................................vi Preface ....................................................................................................................vii Réamhrá................................................................................................................viii Acknowledgements...............................................................................................ix -
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African Journal of Microbiology Research Vol. 5(31), pp. 5750-5756, 23 December, 2011 Available online at http://www.academicjournals.org/AJMR ISSN 1996-0808 ©2011 Academic Journals DOI: 10.5897/AJMR11.1228 Full Length Research Paper Leucocalocybe, a new genus for Tricholoma mongolicum (Agaricales, Basidiomycota) Xiao-Dan Yu1,2, Hui Deng1 and Yi-Jian Yao1,3* 1State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, China. 2Graduate University of Chinese Academy of Sciences, Beijing, 100049, China. 3Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3AB, United Kingdom. Accepted 11 November, 2011 A new genus of Agaricales, Leucocalocybe was erected for a species Tricholoma mongolicum in this study. Leucocalocybe was distinguished from the other genera by a unique combination of macro- and micro-morphological characters, including a tricholomatoid habit, thick and short stem, minutely spiny spores and white spore print. The assignment of the new genus was supported by phylogenetic analyses based on the LSU sequences. The results of molecular analyses demonstrated that the species was clustered in tricholomatoid clade, which formed a distinct lineage. Key words: Agaricales, taxonomy, Tricholoma, tricholomatoid clade. INTRODUCTION The genus Tricholoma (Fr.) Staude is typified by having were re-described. Based on morphological and mole- distinctly emarginate-sinuate lamellae, white or very pale cular analyses, T. mongolicum appears to be aberrant cream spore print, producing smooth thin-walled within Tricholoma and un-subsumable into any of the basidiospores, lacking clamp connections, cheilocystidia extant genera. Accordingly, we proposed to erect a new and pleurocystidia (Singer, 1986). Most species of this genus, Leucocalocybe, to circumscribe the unique genus form obligate ectomycorrhizal associations with combination of features characterizing this fungus and a forest trees, only a few species in the subgenus necessary new combination. -
Mushrooms Commonly Found in Northwest Washington
MUSHROOMS COMMONLY FOUND IN NORTHWEST WASHINGTON GILLED MUSHROOMS SPORES WHITE Amanita constricta Amanita franchettii (A. aspera) Amanita gemmata Amanita muscaria Amanita pachycolea Amanita pantherina Amanita porphyria Amanita silvicola Amanita smithiana Amanita vaginata Armillaria nabsnona (A. mellea) Armillaria ostoyae (A. mellea) Armillaria sinapina (A. mellea) Calocybe carnea Clitocybe avellaneoalba Clitocybe clavipes Clitocybe dealbata Clitocybe deceptiva Clitocybe dilatata Clitocybe flaccida Clitocybe fragrans Clitocybe gigantean Clitocybe ligula Clitocybe nebularis Clitocybe odora Hygrophoropsis (Clitocybe) aurantiaca Lepista (Clitocybe) inversa Lepista (Clitocybe) irina Lepista (Clitocybe) nuda Gymnopus (Collybia) acervatus Gymnopus (Collybia) confluens Gymnopus (Collybia) dryophila Gymnopus (Collybia) fuscopurpureus Gymnopus (Collybia) peronata Rhodocollybia (Collybia) butyracea Rhodocollybia (Collybia) maculata Strobilurus (Collybia) trullisatus Cystoderma cinnabarinum Cystoderma amianthinum Cystoderma fallax Cystoderma granulosum Flammulina velutipes Hygrocybe (Hygrophorus) conica Hygrocybe (Hygrophorus) minuiatus Hygrophorus bakerensis Hygrophorus camarophyllus Hygrophorus piceae Laccaria amethysteo-occidentalis Laccaria bicolor Laccaria laccata Lactarius alnicola Lactarius deliciousus Lactarius fallax Lactarius kaufmanii Lactarius luculentus Lactarius obscuratus Lactarius occidentalis Lactarius pallescens Lactarius parvis Lactarius pseudomucidus Lactarius pubescens Lactarius repraesentaneus Lactarius rubrilacteus Lactarius -
Notes on Clitocybe S. Lato (Agaricales)
Ann. Bot. Fennici 40: 213–218 ISSN 0003-3847 Helsinki 19 June 2003 © Finnish Zoological and Botanical Publishing Board 2003 Notes on Clitocybe s. lato (Agaricales) Harri Harmaja Botanical Museum, Finnish Museum of Natural History, P.O Box 7, FIN-00014 University of Helsinki, Finland (e-mail: harri.harmaja@helsinki.fi ) Received 7 Feb. 2003, revised version received 28 Mar. 2003, accepted 1 Apr. 2003 Harmaja, H. 2003: Notes on Clitocybe s. lato (Agaricales). — Ann. Bot. Fennici 40: 213–218. Agaricus nebularis Batsch : Fr. is approved as the lectotype of the genus Clitocybe (Fr.) Staude (Agaricales: Tricholomataceae). Lepista (Fr.) W.G. Smith is a younger taxonomic synonym. Diagnostic characters of Clitocybe are discussed; among the less known ones are: (i) a proportion of the detached spores adhere in tetrads in microscopic mounts, (ii) the spore wall is cyanophilic, and (iii) the mycelium is capable of reducing nitrate. Three new nomenclatural combinations in Clitocybe are made. The new genus Infundibulicybe Harmaja, with Agaricus gibbus Pers. : Fr. as the type, is segregated for the core group of those species of Clitocybe s. lato that do not fi t to the genus as defi ned here. Infundibulicybe mainly differs from Clitocybe in that: (i) the spores do not adhere in tetrads, (ii) all or a proportion of the spores have confl uent bases, (iii) all or most of the spores are lacrymoid in shape, (iv) the spore wall is cyanophobic, and (v) the mycelium is incapable of reducing nitrate. Thirteen new nomenclatural combinations in Infundibulicybe are made. Two new nomenclatural combinations are made in Ampulloclitocybe Redhead, Lutzoni, Moncalvo & Vilgalys (syn. -
Fungal Survey of the Wye Valley Woodlands Special Area of Conservation (SAC) Alan Lucas Freelance Ecologist
Fungal Survey of the Wye Valley Woodlands Special Area of Conservation (SAC) Alan Lucas Freelance Ecologist NRW Evidence Report No 242 Date www.naturalresourceswales.gov.uk About Natural Resources Wales Natural Resources Wales’ purpose is to pursue sustainable management of natural resources. This means looking after air, land, water, wildlife, plants and soil to improve Wales’ well-being, and provide a better future for everyone. Evidence at Natural Resources Wales Natural Resources Wales is an evidence based organisation. We seek to ensure that our strategy, decisions, operations and advice to Welsh Government and others are underpinned by sound and quality-assured evidence. We recognise that it is critically important to have a good understanding of our changing environment. We will realise this vision by: Maintaining and developing the technical specialist skills of our staff; Securing our data and information; Having a well resourced proactive programme of evidence work; Continuing to review and add to our evidence to ensure it is fit for the challenges facing us; and Communicating our evidence in an open and transparent way. This Evidence Report series serves as a record of work carried out or commissioned by Natural Resources Wales. It also helps us to share and promote use of our evidence by others and develop future collaborations. However, the views and recommendations presented in this report are not necessarily those of NRW and should, therefore, not be attributed to NRW. www.naturalresourceswales.gov.uk Page 2 Report -
Ecography ECOG-02256 Heegaard, E., Boddy, L., Diez, J
Ecography ECOG-02256 Heegaard, E., Boddy, L., Diez, J. M., Halvorsen, R., Kauserud, H., Kuyper, T. W., Bässler, C., Büntgen, U., Gange, A. C., Krisai-Greilhuber, I., Andrew, C. J., Ayer, F., Høiland, K., Kirk, P. and Egli, S. 2016. Fine-scale spatiotemporal dynamics of fungal fruiting: prevalence, amplitude, range and continuity. – Ecography doi: 10.1111/ecog.02256 Supplementary material Appendix 1 Table A1. List of species recorded in the period 1992-2006, functional categorization of the individual species and how many records present of each species. Species names Functional group Records Agaricus dulcidulus Saprotrophic 9 Agaricus semotus Saprotrophic 26 Agaricus sylvicola Saprotrophic 17 Agrocybe praecox Saprotrophic 4 Amanita battarrae ECM 2 Amanita citrina ECM 178 Amanita excelsa ECM 11 Amanita fulva ECM 2 Amanita gemmata ECM 140 Amanita muscaria ECM 28 Amanita pantherina ECM 33 Amanita porphyria ECM 90 Amanita rubescens ECM 171 Amanita vaginata ECM 2 Ampulloclitocybe clavipes Saprotrophic 42 Baeospora myosura Saprotrophic 4 Boletus badius ECM 432 Boletus calopus ECM 4 Boletus edulis ECM 75 Boletus erythropus ECM 25 Boletus luridus ECM 2 Boletus reticulatus ECM 20 Boletus subtomentosus ECM 11 Cantharellus cibarius ECM 78 Cantharellus cinereus ECM 30 Cantharellus ianthinoxanthus ECM 60 Chalciporus piperatus ECM 19 Chlorophyllum rachodes Saprotrophic 63 Chroogomphus helveticus ECM 146 Chroogomphus rutilus ECM 3 Clitocybe costata Saprotrophic 3 Clitocybe ditopa Saprotrophic 52 Clitocybe fuligineipes Saprotrophic 30 Clitocybe gibba -
Small, Saprophytic Volvariella Species in the Netherlands
PERSOONIA Published by the Rijksherbarium, Leiden Volume 13, Part 2, pp. 197-211 (1986) Notulae ad Floram agaricinam neerlandicam—XII. Small, saprophytic Volvariella species in the Netherlands T. Boekhout Rijksherbarium, Leiden* Characters used in current taxonomy of the genus Volvariella are discussed. Spore dimensions are a good additional character for distinguishingspecies. Vol- and variella caesiotincta, V. hypopithys, V. murinella, V. pusilla are redescribed. Volvariella murinella f. brevispora is described and V. taylori is reduced to a variety of V. pusilla. The genus Volvariella has been intensively studied during the last decades (e.g. Shaffer, 1957; Orton, 1974; Courtecuisse, 1984). During our investigations, however, we had problems in identifying small, saprophytic species of Volvariella, such as V. murinella, V. hypopithys, and V. pusilla. According to Orton (1974), the principal diagnostic fea- tures of this genus are the colour of the pileus and volva, the morphology of the volva (two-lobed versus four-lobed), the surface structure of the pileus and stipe, and the habitat. We carefully studied the material available from the Netherlands and tried to of evaluate the characters used in current taxonomy this genus. MORPHOLOGY OF SPORES, VOLVA AND SURFACE STRUCTURES Our observations indicate that in Volvariella the colour of both pileus and volva is rather variable. But the dimensions of the spores seem to be a good additional character for delimitating species (Figs. 1, 2). Volvariella murinella is well characterized by nar- row, elongate ellipsoid to subcylindrical spores, 5.5—8.0 x 3.0-4.5 ptm, Q \.5-^175(Fig. of of from white 1). In one collection, the colour the pileus this species ranges entirely with umbo with brownish Bas a pale grey-brown to grey-brown a grey centre ( 6596, L). -
Entoloma Sinuatum
© Demetrio Merino Alcántara [email protected] Condiciones de uso Entoloma sinuatum (Bull.) P. Kumm., Führ. Pilzk. (Zerbst): 97 (1871) Entolomataceae, Agaricales, Agaricomycetidae, Agaricomycetes, Agaricomycotina, Basidiomycota, Fungi ≡ Agaricus arenarius (Laterrade) Lév., Annls Sci. Nat., Bot., sér. 3 9: 119 (1848) = Agaricus lividus Bull., Herb. Fr. (Paris) 8: tab. 382 (1788) = Agaricus lividus var. roseus Cooke, Illustrations of British Fungi (Hymenomycetes) (London) 3: pl. 318 (469) (1884) ≡ Agaricus sinuatus Bull., Herb. Fr. (Paris) 13: tab. 579, fig. 1 (1793) ≡ Agaricus sinuatus var. arenarius Laterrade, Flore bordelaise, Edition 4: 534 (2009) ≡ Agaricus sinuatus var. carmelinus Lasch, Linnaea 4: 538 (1829) ≡ Agaricus sinuatus var. cavipes Lasch, Linnaea 4: 538 (1829) = Agaricus sinuatus Bull., Herb. Fr. (Paris) 13: tab. 579, fig. 1 (1793) var. sinuatus = Entoloma camelinum (Lasch) P. Kumm., Führ. Pilzk. (Zerbst): 98 (1871) = Entoloma eulividum Noordel., Persoonia 12(4): 457 (1985) = Entoloma lividum Quél., Mém. Soc. Émul. Montbéliard, Sér. 2 5: 116 (1872) = Entoloma lividum Quél., Mém. Soc. Émul. Montbéliard, Sér. 2 5: 116 (1872) var. lividum = Entoloma lividum var. pratense Niolle, Bull. trimest. Soc. mycol. Fr. 64: 253 (1948) = Entoloma lividum var. roseum (Cooke) Sacc., Syll. fung. (Abellini) 5: 680 (1887) ≡ Entoloma sinuatum var. camelinum (Lasch) Sacc., Syll. fung. (Abellini) 5: 680 (1887) ≡ Entoloma sinuatum (Bull.) P. Kumm., Führ. Pilzk. (Zerbst): 23, 97 (1871) var. sinuatum = Rhodophyllus lividus (Quél.) Quél., Enchir. fung. (Paris): 57 (1886) ≡ Rhodophyllus sinuatus (Bull.) Quél., Fl. mycol. France (Paris): 179 (1888) Material estudiado: Francia, Aquitania, Osse en Aspe, Pierre St. Martin, 30TXN8663, 931 m, en suelo bajo Fagus sylvatica y Abies alba, 16-VII-2016, leg. Carmen Mari Jiménez, Dianora Estrada, Manuel Plaza y Demetrio Merino, JA-CUSSTA: 8903. -
Major Clades of Agaricales: a Multilocus Phylogenetic Overview
Mycologia, 98(6), 2006, pp. 982–995. # 2006 by The Mycological Society of America, Lawrence, KS 66044-8897 Major clades of Agaricales: a multilocus phylogenetic overview P. Brandon Matheny1 Duur K. Aanen Judd M. Curtis Laboratory of Genetics, Arboretumlaan 4, 6703 BD, Biology Department, Clark University, 950 Main Street, Wageningen, The Netherlands Worcester, Massachusetts, 01610 Matthew DeNitis Vale´rie Hofstetter 127 Harrington Way, Worcester, Massachusetts 01604 Department of Biology, Box 90338, Duke University, Durham, North Carolina 27708 Graciela M. Daniele Instituto Multidisciplinario de Biologı´a Vegetal, M. Catherine Aime CONICET-Universidad Nacional de Co´rdoba, Casilla USDA-ARS, Systematic Botany and Mycology de Correo 495, 5000 Co´rdoba, Argentina Laboratory, Room 304, Building 011A, 10300 Baltimore Avenue, Beltsville, Maryland 20705-2350 Dennis E. Desjardin Department of Biology, San Francisco State University, Jean-Marc Moncalvo San Francisco, California 94132 Centre for Biodiversity and Conservation Biology, Royal Ontario Museum and Department of Botany, University Bradley R. Kropp of Toronto, Toronto, Ontario, M5S 2C6 Canada Department of Biology, Utah State University, Logan, Utah 84322 Zai-Wei Ge Zhu-Liang Yang Lorelei L. Norvell Kunming Institute of Botany, Chinese Academy of Pacific Northwest Mycology Service, 6720 NW Skyline Sciences, Kunming 650204, P.R. China Boulevard, Portland, Oregon 97229-1309 Jason C. Slot Andrew Parker Biology Department, Clark University, 950 Main Street, 127 Raven Way, Metaline Falls, Washington 99153 Worcester, Massachusetts, 01609 9720 Joseph F. Ammirati Else C. Vellinga University of Washington, Biology Department, Box Department of Plant and Microbial Biology, 111 355325, Seattle, Washington 98195 Koshland Hall, University of California, Berkeley, California 94720-3102 Timothy J. -
Checklist of Indiana Fungi I: Macrofungi
2017. Proceedings of the Indiana Academy of Science 126(1):12–34 CHECKLIST OF INDIANA FUNGI I: MACROFUNGI Scott T. Bates1, Justin Golday, Rachel L. Kunnen2 and Nathanael J. Pilla3: Department of Biological Sciences, Purdue University Northwest, Westville, IN 46391 USA ABSTRACT. A checklist of macrofungi was compiled for Indiana as part of a larger effort to document fungi within the state. Our study compiled records of Indiana fungi from digitized specimen data available online through the Mycology Collections data Portal (http://mycoportal.org). These data were supplemented with records from the scientific literature. While several small checklists of Indiana fungi exist, the majority of these being published previously in the Proceeding of the Indiana Academy of Science, our study represents the first to comprehensively compile all the available data on Indiana fungi. Overall, more than 19,000 records of Indiana fungi were examined, with 1410 species of macrofungi being documented in this publication. These species represent 24 fungal orders from two major phyla, with 757 species in this checklist being reported in the literature for the first time here. Our study also recovered records documenting other groups of Indiana fungi, such as microfungi, which will be covered in subsequent publications. Keywords: Ascomycota, Basidiomycota, checklist, Eumycota, fungi, taxonomy INTRODUCTION Members of the kingdom Eumycota (Fungi) are filamentous, or sometimes unicellular, hetero- A wide range of natural communities exist in trophic organisms -
Major Clades of Agaricales: a Multilocus Phylogenetic Overview
Mycologia, 98(6), 2006, pp. 982–995. # 2006 by The Mycological Society of America, Lawrence, KS 66044-8897 Major clades of Agaricales: a multilocus phylogenetic overview P. Brandon Matheny1 Duur K. Aanen Judd M. Curtis Laboratory of Genetics, Arboretumlaan 4, 6703 BD, Biology Department, Clark University, 950 Main Street, Wageningen, The Netherlands Worcester, Massachusetts, 01610 Matthew DeNitis Vale´rie Hofstetter 127 Harrington Way, Worcester, Massachusetts 01604 Department of Biology, Box 90338, Duke University, Durham, North Carolina 27708 Graciela M. Daniele Instituto Multidisciplinario de Biologı´a Vegetal, M. Catherine Aime CONICET-Universidad Nacional de Co´rdoba, Casilla USDA-ARS, Systematic Botany and Mycology de Correo 495, 5000 Co´rdoba, Argentina Laboratory, Room 304, Building 011A, 10300 Baltimore Avenue, Beltsville, Maryland 20705-2350 Dennis E. Desjardin Department of Biology, San Francisco State University, Jean-Marc Moncalvo San Francisco, California 94132 Centre for Biodiversity and Conservation Biology, Royal Ontario Museum and Department of Botany, University Bradley R. Kropp of Toronto, Toronto, Ontario, M5S 2C6 Canada Department of Biology, Utah State University, Logan, Utah 84322 Zai-Wei Ge Zhu-Liang Yang Lorelei L. Norvell Kunming Institute of Botany, Chinese Academy of Pacific Northwest Mycology Service, 6720 NW Skyline Sciences, Kunming 650204, P.R. China Boulevard, Portland, Oregon 97229-1309 Jason C. Slot Andrew Parker Biology Department, Clark University, 950 Main Street, 127 Raven Way, Metaline Falls, Washington 99153- Worcester, Massachusetts, 01609 9720 Joseph F. Ammirati Else C. Vellinga University of Washington, Biology Department, Box Department of Plant and Microbial Biology, 111 355325, Seattle, Washington 98195 Koshland Hall, University of California, Berkeley, California 94720-3102 Timothy J.