Ecography ECOG-02256 Heegaard, E., Boddy, L., Diez, J

Total Page:16

File Type:pdf, Size:1020Kb

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 Saprotrophic 1104 Clitocybe houghtonii Saprotrophic 278 Clitocybe metachroa Saprotrophic 29 Clitocybe nebularis Saprotrophic 314 Clitocybe obsoleta Saprotrophic 1 Clitocybe odora Saprotrophic 1 Clitocybe phaeophthalma Saprotrophic 4 Clitocybe phyllophila Saprotrophic 3 Clitocybe suaveolens Saprotrophic 12 Clitocybe subspadicea Saprotrophic 83 Clitocybe umbilicata Saprotrophic 81 Clitocybe vibecina Saprotrophic 80 Clitopilus prunulus Saprotrophic 4 Collybia ozes Saprotrophic 6 Conocybe pygmaeoaffinis Saprotrophic 12 Conocybe vestita Saprotrophic 1 Coprinellus domesticus Saprotrophic 118 Coprinellus micaceus Saprotrophic 80 Cortinarius acutus ECM 135 Cortinarius alboviolaceus ECM 3 Cortinarius anomalus ECM 292 Cortinarius anserinus ECM 28 Cortinarius anthracinus ECM 2 Cortinarius armeniacus ECM 53 Cortinarius betuletorum ECM 179 Cortinarius bivelus ECM 7 Cortinarius bolaris ECM 398 Cortinarius callochrous ECM 47 Cortinarius caperatus ECM 1078 Cortinarius casimiri ECM 276 Cortinarius causticus ECM 6 Cortinarius cinnamomeus ECM 1 Cortinarius citrinus ECM 76 Cortinarius claricolor ECM 5 Cortinarius cliduchus ECM 160 Cortinarius crystallinus ECM 32 Cortinarius damascenus ECM 166 Cortinarius decipiens ECM 355 Cortinarius eburneus ECM 3 Cortinarius elatior ECM 18 Cortinarius epipoleus ECM 4 Cortinarius evernius ECM 24 Cortinarius flexipes ECM 1480 Cortinarius glaucopus ECM 10 Cortinarius hinnuleus ECM 1 Cortinarius humicola ECM 6 Cortinarius infractus ECM 19 Cortinarius largus ECM 247 Cortinarius malachius ECM 4 Cortinarius malicorius ECM 1 Cortinarius meinhardii ECM 1 Cortinarius multiformis ECM 75 Cortinarius odorifer ECM 3 Cortinarius paragaudis ECM 98 Cortinarius parvannulatus ECM 18 Cortinarius pilatii ECM 9 Cortinarius porphyropus ECM 2 Cortinarius purpurascens ECM 11 Cortinarius rigens ECM 56 Cortinarius sanguineus ECM 6 Cortinarius sebaceus ECM 56 Cortinarius spilomeus ECM 7 Cortinarius stillatitius ECM 2 Cortinarius subporphyropus ECM 32 Cortinarius talus ECM 1 Cortinarius torvus ECM 3 Cortinarius uraceus ECM 1 Cortinarius variicolor ECM 1 Cortinarius varius ECM 1 Cortinarius venetus ECM 12 Cortinarius vibratilis ECM 12 Cortinarius vulpinus ECM 30 Craterellus cornucopioides ECM 4099 Craterellus tubaeformis ECM 619 Crepidotus cesatii Saprotrophic 22 Cystoderma amianthinum Saprotrophic 409 Cystoderma carcharias Saprotrophic 29 Cystodermella granulosa Saprotrophic 10 Cystolepiota seminuda Saprotrophic 19 Entocybe nitida Saprotrophic 11 Entocybe turbida Saprotrophic 6 Entoloma cetratum Saprotrophic 10 Entoloma conferendum Saprotrophic 15 Entoloma cuneatum Saprotrophic 6 Entoloma lividoalbum Saprotrophic 21 Entoloma rhodopolium Saprotrophic 641 Flammulaster carpophilus Saprotrophic 3 Galerella plicatella Saprotrophic 2 Galerina marginata Saprotrophic 122 Galerina stylifera Saprotrophic 4 Galerina uncialis Saprotrophic 88 Gymnopilus hybridus Saprotrophic 98 Gymnopus confluens Saprotrophic 971 Gymnopus dryophilus Saprotrophic 645 Gymnopus erythropus Saprotrophic 58 Gymnopus fuscopurpureus Saprotrophic 159 Gymnopus ocior Saprotrophic 189 Gymnopus peronatus Saprotrophic 190 Hebeloma crustuliniforme ECM 64 Hebeloma mesophaeum ECM 8 Hebeloma radicosum ECM 6 Hebeloma spoliatum ECM 4 Hohenbuehelia myxotricha Saprotrophic 1 Hydnum repandum ECM 345 Hydnum rufescens ECM 116 Hydropus subalpinus Saprotrophic 4 Hygrophoropsis aurantiaca Saprotrophic 75 Hygrophorus eburneus ECM 1178 Hygrophorus mesotephrus ECM 9 Hygrophorus pustulatus ECM 8 Hymenopellis radicata Saprotrophic 166 Hypholoma capnoides Saprotrophic 94 Hypholoma fasciculare Saprotrophic 6721 Hypholoma lateritium Saprotrophic 220 Hypholoma radicosum Saprotrophic 2 Inocybe acuta ECM 2 Inocybe assimilata ECM 22 Inocybe asterospora ECM 8 Inocybe catalaunica ECM 197 Inocybe cincinnata ECM 29 Inocybe cookei ECM 7 Inocybe flocculosa ECM 62 Inocybe fuscidula ECM 2 Inocybe geophylla ECM 33 Inocybe griseolilacina ECM 29 Inocybe hirtella ECM 454 Inocybe nitidiuscula ECM 45 Inocybe petiginosa ECM 970 Inocybe pusio ECM 4 Inocybe transitoria ECM 19 Kuehneromyces mutabilis Saprotrophic 6946 Laccaria amethystina ECM 8512 Laccaria bicolor ECM 4 Laccaria laccata ECM 1425 Lactarius acris ECM 34 Lactarius albocarneus ECM 1 Lactarius aurantiacus ECM 130 Lactarius blennius ECM 2331 Lactarius camphoratus ECM 360 Lactarius cremor ECM 13 Lactarius deterrimus ECM 26 Lactarius fuliginosus ECM 30 Lactarius pallidus ECM 126 Lactarius pergamenus ECM 2 Lactarius picinus ECM 2 Lactarius piperatus ECM 169 Lactarius porninsis ECM 10 Lactarius pterosporus ECM 12 Lactarius quietus ECM 2 Lactarius romagnesii ECM 1 Lactarius rufus ECM 2 Lactarius subdulcis ECM 83 Lactarius uvidus ECM 5 Lactarius vellereus ECM 2 Lactarius volemus ECM 5 Lentinellus cochleatus Saprotrophic 9 Lepiota clypeolaria Saprotrophic 18 Lepiota cristata Saprotrophic 2 Lepiota magnispora Saprotrophic 16 Lepista flaccida Saprotrophic 47 Lepista nuda Saprotrophic 3 Leucocortinarius bulbiger Saprotrophic 1 Lyophyllum decastes Saprotrophic 10 Lyophyllum fumosum Saprotrophic 4 Macrocystidia cucumis Saprotrophic 5 Macrolepiota excoriata Saprotrophic 1 Macrolepiota procera Saprotrophic 9 Marasmius cohaerens Saprotrophic 25 Marasmius torquescens Saprotrophic 592 Marasmius wynneae Saprotrophic 10 Megacollybia platyphylla Saprotrophic 136 Melanoleuca melaleuca Saprotrophic 3 Mycena diosma Saprotrophic 53 Mycena epipterygia Saprotrophic 108 Mycena flavescens Saprotrophic 13 Mycena galericulata Saprotrophic 21 Mycena galopus Saprotrophic 1170 Mycena haematopus Saprotrophic 6 Mycena pelianthina Saprotrophic 251 Mycena polygramma Saprotrophic 1 Mycena pura Saprotrophic 1857 Mycena rosea Saprotrophic 228 Mycena sanguinolenta Saprotrophic 95 Mycena vitilis Saprotrophic 5 Mycena zephirus Saprotrophic 27 Oudemansiella mucida Saprotrophic 114 Panellus stipticus Saprotrophic 17 Phaeocollybia arduennensis ECM 4 Pholiota astragalina Saprotrophic 3 Pholiota squarrosa Saprotrophic 706 Pluteus brunneoradiatus Saprotrophic 2 Pluteus cervinus Saprotrophic 50 Pluteus exiguus Saprotrophic 20 Pluteus nanus Saprotrophic 11 Pluteus romellii Saprotrophic 1 Pluteus satur Saprotrophic 1 Psathyrella dicrani Saprotrophic 5 Psathyrella piluliformis Saprotrophic 543 Pseudoclitocybe cyathiformis Saprotrophic 72 Pseudocraterellus undulatus ECM 228 Pseudoomphalina compressipes Saprotrophic 15 Psilocybe crobula Saprotrophic 2 Psilocybe phyllogena Saprotrophic 3 Rhodocollybia butyracea Saprotrophic 4843 Rhodocollybia maculata Saprotrophic 17 Rhodocollybia prolixa Saprotrophic 366 Rickenella fibula Saprotrophic 13 Ripartites tricholoma Saprotrophic 1 Rugosomyces carneus Saprotrophic 3 Russula acrifolia ECM 447 Russula albonigra ECM 4 Russula amethystina ECM 2 Russula aurora ECM 204 Russula chloroides ECM 10 Russula cyanoxantha ECM 618 Russula delica ECM 21 Russula densifolia ECM 6 Russula faginea ECM 5 Russula fellea ECM 800 Russula foetens ECM 132 Russula fragilis ECM 3 Russula grata ECM 28 Russula grisea ECM 106 Russula heterophylla ECM 2 Russula illota ECM 2 Russula integra ECM 26 Russula langei ECM 14 Russula minutula ECM 2 Russula nauseosa ECM 2 Russula nigricans ECM 443 Russula nobilis ECM 2268 Russula ochroleuca ECM 3811 Russula postiana ECM 2 Russula pseudointegra ECM 1 Russula puellaris ECM 36 Russula queletii ECM 10 Russula raoultii ECM 13 Russula risigallina ECM 4 Russula romellii ECM 97 Russula rosea ECM 20 Russula rubra ECM 34 Russula vesca ECM 28 Russula virescens ECM 5 Sarcomyxa serotina Saprotrophic 15 Stropharia aeruginosa Saprotrophic 47 Suillus bovinus ECM 7 Suillus grevillei ECM 300 Suillus viscidus ECM 168 Tapinella atrotomentosa Saprotrophic 92 Tapinella panuoides Saprotrophic 2 Tephrocybe boudieri Saprotrophic 2 Tephrocybe inolens Saprotrophic 1 Tephrocybe murina Saprotrophic 38 Tephrocybe putida Saprotrophic 9 Tephrocybe rancida Saprotrophic 59 Trichocybe puberula Saprotrophic 2 Tricholoma bufonium ECM 1 Tricholoma inamoenum ECM 48 Tricholoma saponaceum ECM 6 Tricholoma sciodes ECM 120 Tricholoma sulphureum ECM 12 Tricholoma terreum
Recommended publications
  • Molecular Phylogenetic Studies in the Genus Amanita
    1170 Molecular phylogenetic studies in the genus Amanita I5ichael Weiß, Zhu-Liang Yang, and Franz Oberwinkler Abstracl A group of 49 Amanita species that had been thoroughly examined morphologically and amtomically was analyzed by DNA sequence compadson to estimate natural groups and phylogenetic rclationships within the genus. Nuclear DNA sequences coding for a part of the ribosomal large subunit were determined and evaluated using neighbor-joining with bootstrap analysis, parsimony analysis, conditional clustering, and maximum likelihood methods, Sections Amanita, Caesarea, Vaginatae, Validae, Phalloideae, and Amidella were substantially confirmed as monophyletic groups, while the monophyly of section Lepidell.t remained unclear. Branching topologies between and within sections could also pafiially be derived. Stbgenera Amanita an'd Lepidella were not supported. The Mappae group was included in section Validae. Grouping hypotheses obtained by DNA analyses are discussed in relation to the distribution of morphological and anatomical chamcters in the studied species. Key words: fungi, basidiomycetes phylogeny, Agarrcales, Amanita systematics, large subunit rDNA, 28S. R6sum6 : A partir d'un groupe de 49 esp,ces d'Amanita prdalablement examinees morphologiquement et anatomiquement, les auteurs ont utilisd la comparaison des s€quences d'ADN pour ddfinir les groupes naturels et les relations phylog6ndtiques de ce genre. Les sdquences de I'ADN nucl6aire codant pour une partie de la grande sous-unit6 ribosomale ont 6t6 ddterminEes et €valu6es en utilisant l'analyse par liaison en lacet avec le voisin (neighbor-joining with bootstrap), l'analyse en parcimonie, le rcgroupement conditionnel et les m€thodes de ressemblance maximale. Les rdsultats confirment substantiellement les sections Afiarira, Caesarea, Uaqinatae, Ualidae, Phalloideae et Amidella, comme groupes monophyldtiques, alors que la monophylie de la section Lepidella demerxe obscure.
    [Show full text]
  • Boletus Mushrooms La Tia Jackson, Ian C
    Genetic Diversity within Alaskan Boletus Mushrooms www.fungi-zette.com La Tia Jackson, Ian C. Herriott, József Geml, Gary A. Laursen, D. Lee Taylor Discussion Abstract •Clade 1 is composed of Alaskan samples from the interior and Northwest and We analyzed the genetic differences within the collection of samples from Europe. Although the species names do not match up they are genetically very similar, and B. citrinovirens is thought to be in what is called the Boletus mushroom from the UAF Fungal Herbarium, representing Identification on Tree Location subtomentosus group. samples from all over Alaska. Upon analyzing the DNA sequence Results DQ066405_Boletus_citrinovirens Europe from 18 samples, we found that most Alaskan Boletus are closely DQ066407_Boletus_spadiceus Europe •Clade 2 is composed of Alaskan samples from Southeast Alaska and GenBank DQ066397_Boletus_citrinovirens Europe samples from Europe, both identified as Boletus mirabilis. related to samples from the same species found in other parts of the world (clades 1,2,5,6,8,12). We also found that some species DQ066410_Boletus_spadiceus Europe •Clade 3 is composed of samples only from Alaska. None of the sequences DQ384578_Boletellus_mirabilis Europe collected in other parts of the world were not found in our sample 1 mycorance.free.fr obtained from GenBank are closely related. These were morphologically collection (clades 4,7,9,10,11). Finally, our results suggested that AJ419187_Boletus_impolitus Spain identified as B. subglabripes. “B. subglabripes” is in GenBank, but only Large 100 DQ131632_Xerocomus_subtomentosus Europe clade 3 on our phylogenetic tree is not represented among the Subunit gene, not Internally Transcribed Spacer gene (reference 2) so comparison AJ889931_Boletus_pruinatus Europe GenBank sequences from other parts of the world and may be a 100 is not possible to determine if morphological species attribution is the same or 2 AM087271_Xerocomus_pruinatus Europe genetic lineage endemic to Alaska.
    [Show full text]
  • Influence of Tree Species on Richness and Diversity of Epigeous Fungal
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Archive Ouverte en Sciences de l'Information et de la Communication fungal ecology 4 (2011) 22e31 available at www.sciencedirect.com journal homepage: www.elsevier.com/locate/funeco Influence of tree species on richness and diversity of epigeous fungal communities in a French temperate forest stand Marc BUE´Ea,*, Jean-Paul MAURICEb, Bernd ZELLERc, Sitraka ANDRIANARISOAc, Jacques RANGERc,Re´gis COURTECUISSEd, Benoıˆt MARC¸AISa, Franc¸ois LE TACONa aINRA Nancy, UMR INRA/UHP 1136 Interactions Arbres/Microorganismes, 54280 Champenoux, France bGroupe Mycologique Vosgien, 18 bis, place des Cordeliers, 88300 Neufchaˆteau, France cINRA Nancy, UR 1138 Bioge´ochimie des Ecosyste`mes Forestiers, 54280 Champenoux, France dUniversite´ de Lille, Faculte´ de Pharmacie, F59006 Lille, France article info abstract Article history: Epigeous saprotrophic and ectomycorrhizal (ECM) fungal sporocarps were assessed during Received 30 September 2009 7 yr in a French temperate experimental forest site with six 30-year-old mono-specific Revision received 10 May 2010 plantations (four coniferous and two hardwood plantations) and one 150-year-old native Accepted 21 July 2010 mixed deciduous forest. A total of 331 fungal species were identified. Half of the fungal Available online 6 October 2010 species were ECM, but this proportion varied slightly by forest composition. The replace- Corresponding editor: Anne Pringle ment of the native forest by mono-specific plantations, including native species such as beech and oak, considerably altered the diversity of epigeous ECM and saprotrophic fungi. Keywords: Among the six mono-specific stands, fungal diversity was the highest in Nordmann fir and Conifer plantation Norway spruce plantations and the lowest in Corsican pine and Douglas fir plantations.
    [Show full text]
  • Reviewing the World's Edible Mushroom Species: a New
    Received: 5 September 2020 Revised: 4 December 2020 Accepted: 21 December 2020 DOI: 10.1111/1541-4337.12708 COMPREHENSIVE REVIEWS IN FOOD SCIENCE AND FOOD SAFETY Reviewing the world’s edible mushroom species: A new evidence-based classification system Huili Li1,2,3 Yang Tian4 Nelson Menolli Jr5,6 Lei Ye1,2,3 Samantha C. Karunarathna1,2,3 Jesus Perez-Moreno7 Mohammad Mahmudur Rahman8 Md Harunur Rashid8 Pheng Phengsintham9 Leela Rizal10 Taiga Kasuya11 Young Woon Lim12 Arun Kumar Dutta13 Abdul Nasir Khalid14 Le Thanh Huyen15 Marilen Parungao Balolong16 Gautam Baruah17 Sumedha Madawala18 Naritsada Thongklang19,20 Kevin D. Hyde19,20,21 Paul M. Kirk22 Jianchu Xu1,2,3 Jun Sheng23 Eric Boa24 Peter E. Mortimer1,3 1 CAS Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan, China 2 East and Central Asia Regional Office, World Agroforestry Centre (ICRAF), Kunming, Yunnan, China 3 Centre for Mountain Futures, Kunming Institute of Botany, Kunming, Yunnan, China 4 College of Food Science and Technology, Yunnan Agricultural University, Kunming, Yunnan, China 5 Núcleo de Pesquisa em Micologia, Instituto de Botânica, São Paulo, Brazil 6 Departamento de Ciências da Natureza e Matemática (DCM), Subárea de Biologia (SAB), Instituto Federal de Educação, Ciência e Tecnologia de São Paulo (IFSP), São Paulo, Brazil 7 Colegio de Postgraduados, Campus Montecillo, Texcoco, México 8 Global Centre for Environmental Remediation (GCER), Faculty of Science, The University of Newcastle,
    [Show full text]
  • Pt Reyes Species As of 12-1-2017 Abortiporus Biennis Agaricus
    Pt Reyes Species as of 12-1-2017 Abortiporus biennis Agaricus augustus Agaricus bernardii Agaricus californicus Agaricus campestris Agaricus cupreobrunneus Agaricus diminutivus Agaricus hondensis Agaricus lilaceps Agaricus praeclaresquamosus Agaricus rutilescens Agaricus silvicola Agaricus subrutilescens Agaricus xanthodermus Agrocybe pediades Agrocybe praecox Alboleptonia sericella Aleuria aurantia Alnicola sp. Amanita aprica Amanita augusta Amanita breckonii Amanita calyptratoides Amanita constricta Amanita gemmata Amanita gemmata var. exannulata Amanita calyptraderma Amanita calyptraderma (white form) Amanita magniverrucata Amanita muscaria Amanita novinupta Amanita ocreata Amanita pachycolea Amanita pantherina Amanita phalloides Amanita porphyria Amanita protecta Amanita velosa Amanita smithiana Amaurodon sp. nova Amphinema byssoides gr. Annulohypoxylon thouarsianum Anthrocobia melaloma Antrodia heteromorpha Aphanobasidium pseudotsugae Armillaria gallica Armillaria mellea Armillaria nabsnona Arrhenia epichysium Pt Reyes Species as of 12-1-2017 Arrhenia retiruga Ascobolus sp. Ascocoryne sarcoides Astraeus hygrometricus Auricularia auricula Auriscalpium vulgare Baeospora myosura Balsamia cf. magnata Bisporella citrina Bjerkandera adusta Boidinia propinqua Bolbitius vitellinus Suillellus (Boletus) amygdalinus Rubroboleus (Boletus) eastwoodiae Boletus edulis Boletus fibrillosus Botryobasidium longisporum Botryobasidium sp. Botryobasidium vagum Bovista dermoxantha Bovista pila Bovista plumbea Bulgaria inquinans Byssocorticium californicum
    [Show full text]
  • CZECH MYCOLOGY Publication of the Czech Scientific Society for Mycology
    CZECH MYCOLOGY Publication of the Czech Scientific Society for Mycology Volume 57 August 2005 Number 1-2 Central European genera of the Boletaceae and Suillaceae, with notes on their anatomical characters Jo s e f Š u t a r a Prosetická 239, 415 01 Tbplice, Czech Republic Šutara J. (2005): Central European genera of the Boletaceae and Suillaceae, with notes on their anatomical characters. - Czech Mycol. 57: 1-50. A taxonomic survey of Central European genera of the families Boletaceae and Suillaceae with tubular hymenophores, including the lamellate Phylloporus, is presented. Questions concerning the delimitation of the bolete genera are discussed. Descriptions and keys to the families and genera are based predominantly on anatomical characters of the carpophores. Attention is also paid to peripheral layers of stipe tissue, whose anatomical structure has not been sufficiently studied. The study of these layers, above all of the caulohymenium and the lateral stipe stratum, can provide information important for a better understanding of relationships between taxonomic groups in these families. The presence (or absence) of the caulohymenium with spore-bearing caulobasidia on the stipe surface is here considered as a significant ge­ neric character of boletes. A new combination, Pseudoboletus astraeicola (Imazeki) Šutara, is proposed. Key words: Boletaceae, Suillaceae, generic taxonomy, anatomical characters. Šutara J. (2005): Středoevropské rody čeledí Boletaceae a Suillaceae, s poznámka­ mi k jejich anatomickým znakům. - Czech Mycol. 57: 1-50. Je předložen taxonomický přehled středoevropských rodů čeledí Boletaceae a. SuiUaceae s rourko- vitým hymenoforem, včetně rodu Phylloporus s lupeny. Jsou diskutovány otázky týkající se vymezení hřibovitých rodů. Popisy a klíče k čeledím a rodům jsou založeny převážně na anatomických znacích plodnic.
    [Show full text]
  • Catalogue No. 121 – Sale, Special Offers and Recent Acquisitions
    C. Arden, Bookseller Darren Bloodworth The Nursery, Forest Road, Hay-on-Wye, HR3 5DT, U.K. Tel: +44 (0) 1497-820471 Email: [email protected] Web: www.ardenbooks.co.uk Catalogue No. 121 – Sale, Special Offers and Recent Acquisitions Sale items : Botany 1 - 112 Entomology 113 - 140 Fine, Illustrated & Antiquarian 141 - 151 Gardening 152 - 207 General 208 - 254 Natural History & Zoology 255 - 266 New Naturalist s 267 - 302 Ornithology 303 - 346 Special offers : Botany 347 - 404 and recent Entomology 405 - 440 acquisitions Fine, Illustrated & Antiquarian 441 - 458 Gardening 459 - 512 Natural History & Zoology 513 - 562 New Naturalists 563 - 611 Ornithology 612 - 688 The stock in the Sale part of this catalogue (items 1 to 346) is an attempt to clear the remains of stock from the year’s previous catalogues. Book prices have already been reduced in many cases and further reductions are available to those who wish to take a risk that their chosen books will be available 10 or even 20 days after receiving this catalogue. Books will be dispatched once orders are complete – this may take up to three weeks if you order books at 50% off. How the Sale works First 10 days of sale…….All books available at prices shown in the catalogue After 10 days……………..If books are still available, we reduce their prices by 25% After 20 days……………..If books are still available, we reduce their prices by 50% We have also included over three hundred Special offers and recent acquisitions at the end of the catalogue (items 347 to 688). These Special offers and recent acquisitions are available at the prices indicated and are not part of the Sale terms.
    [Show full text]
  • 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.
    [Show full text]
  • 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
    [Show full text]
  • And Interspecific Hybridiation in Agaric Fungi
    Mycologia, 105(6), 2013, pp. 1577–1594. DOI: 10.3852/13-041 # 2013 by The Mycological Society of America, Lawrence, KS 66044-8897 Evolutionary consequences of putative intra- and interspecific hybridization in agaric fungi Karen W. Hughes1 to determine the outcome of hybridization events. Ronald H. Petersen Within Armillaria mellea and Amanita citrina f. Ecology and Evolutionary Biology, University of lavendula, we found evidence of interbreeding and Tennessee, Knoxville, Tennessee 37996-1100 recombination. Within G. dichrous and H. flavescens/ D. Jean Lodge chlorophana, hybrids were identified but there was Center for Forest Mycology Research, USDA-Forest no evidence for F2 or higher progeny in natural Service, Northern Research Station, Box 137, Luquillo, populations suggesting that the hybrid fruitbodies Puerto Rico 00773-1377 might be an evolutionary dead end and that the Sarah E. Bergemann genetically divergent Mendelian populations from which they were derived are, in fact, different species. Middle Tennessee State University, Department of Biology, PO Box 60, Murfreesboro Tennessee 37132 The association between ITS haplotype divergence of less than 5% (Armillaria mellea 5 2.6% excluding Kendra Baumgartner gaps; Amanita citrina f. lavendula 5 3.3%) with the USDA-Agricultural Research Service, Department of presence of putative recombinants and greater than Plant Pathology, University of California, Davis, California 95616 5% (Gymnopus dichrous 5 5.7%; Hygrocybe flavescens/ chlorophana 5 14.1%) with apparent failure of F1 2 Rodham E. Tulloss hybrids to produce F2 or higher progeny in popula- PO Box 57, Roosevelt, New Jersey 08555-0057 tions may suggest a correlation between genetic Edgar Lickey distance and reproductive isolation.
    [Show full text]
  • Full-Text (PDF)
    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.
    [Show full text]
  • 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
    [Show full text]