Analyses of the Fungi of the Caribbean Island of Dominica
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BGBM Annual Report 2017–2019
NETWORKING FOR DIVERSITY Annual Report 2017 – 2019 2017 – BGBM BGBM Annual Report 2017 – 2019 Cover image: Research into global biodiversity and its significance for humanity is impossible without networks. The topic of networking can be understood in different ways: in the natural world, with the life processes within an organism – visible in the network of the veins of a leaf or in the genetic diversity in populations of plants – networking takes place by means of pollen, via pollinators or the wind. In the world of research, individual objects, such as a particular plant, are networked with the data obtained from them. Networking is also crucial if this data is to be effective as a knowledge base for solving global issues of the future: collaboration between scientific experts within and across disciplines and with stakeholders at regional, national and international level. Contents Foreword 5 Organisation 56 A network for plants 6 Facts and figures 57 Staff, visiting scientists, doctoral students 57 Key events of 2017 – 2019 10 Affiliated and unsalaried scientists, volunteers 58 BGBM publications 59 When diversity goes online 16 Species newly described by BGBM authors 78 Families and genera newly described by BGBM authors 82 On the quest for diversity 20 Online resources and databases 83 Externally funded projects 87 Invisible diversity 24 Hosted scientific events 2017 – 2019 92 Collections 93 Humboldt 2.0 30 Library 96 BGBM Press: publications 97 Between East and West 36 Botanical Museum 99 Press and public relations 101 At the service of science 40 Visitor numbers 102 Budget 103 A research museum 44 Publication information 104 Hands-on science 50 Our symbol, the corncockle 52 4 5 Foreword BGBM Annual Report 2017 – 2019 We are facing vital challenges. -
Checklist of Argentine Agaricales 4
Checklist of the Argentine Agaricales 4. Tricholomataceae and Polyporaceae 1 2* N. NIVEIRO & E. ALBERTÓ 1Instituto de Botánica del Nordeste (UNNE-CONICET). Sargento Cabral 2131, CC 209 Corrientes Capital, CP 3400, Argentina 2Instituto de Investigaciones Biotecnológicas (UNSAM-CONICET) Intendente Marino Km 8.200, Chascomús, Buenos Aires, CP 7130, Argentina CORRESPONDENCE TO *: [email protected] ABSTRACT— A species checklist of 86 genera and 709 species belonging to the families Tricholomataceae and Polyporaceae occurring in Argentina, and including all the species previously published up to year 2011 is presented. KEY WORDS—Agaricomycetes, Marasmius, Mycena, Collybia, Clitocybe Introduction The aim of the Checklist of the Argentinean Agaricales is to establish a baseline of knowledge on the diversity of mushrooms species described in the literature from Argentina up to 2011. The families Amanitaceae, Pluteaceae, Hygrophoraceae, Coprinaceae, Strophariaceae, Bolbitaceae and Crepidotaceae were previoulsy compiled (Niveiro & Albertó 2012a-c). In this contribution, the families Tricholomataceae and Polyporaceae are presented. Materials & Methods Nomenclature and classification systems This checklist compiled data from the available literature on Tricholomataceae and Polyporaceae recorded for Argentina up to the year 2011. Nomenclature and classification systems followed Singer (1986) for families. The genera Pleurotus, Panus, Lentinus, and Schyzophyllum are included in the family Polyporaceae. The Tribe Polyporae (including the genera Polyporus, Pseudofavolus, and Mycobonia) is excluded. There were important rearrangements in the families Tricholomataceae and Polyporaceae according to Singer (1986) over time to present. Tricholomataceae was distributed in six families: Tricholomataceae, Marasmiaceae, Physalacriaceae, Lyophyllaceae, Mycenaceae, and Hydnaginaceae. Some genera belonging to this family were transferred to other orders, i.e. Rickenella (Rickenellaceae, Hymenochaetales), and Lentinellus (Auriscalpiaceae, Russulales). -
Optimization of Agro-Residues As Substrates for Pleurotus
Wu et al. AMB Expr (2019) 9:184 https://doi.org/10.1186/s13568-019-0907-1 ORIGINAL ARTICLE Open Access Optimization of agro-residues as substrates for Pleurotus pulmonarius production Nan Wu1†, Fenghua Tian1†, Odeshnee Moodley1, Bing Song1, Chuanwen Jia1, Jianqiang Ye2, Ruina Lv1, Zhi Qin3 and Changtian Li1* Abstract The “replacing wood by grass” project can partially resolve the confict between mushroom production and balancing the ecosystem, while promoting agricultural economic sustainability. Pleurotus pulmonarius is an economically impor- tant edible and medicinal mushroom, which is traditionally produced using a substrate consisting of sawdust and cottonseed hulls, supplemented with wheat bran. A simplex lattice design was applied to systemically optimize the cultivation of P. pulmonarius using agro-residues as the main substrate to replace sawdust and cottonseed hulls. The efects of difering amounts of wheat straw, corn straw, and soybean straw on the variables of yield, mycelial growth rate, stipe length, pileus length, pileus width, and time to harvest were demonstrated. Results indicated that a mix of wheat straw, corn straw, and soybean straw may have signifcantly positive efects on each of these variables. The high yield comprehensive formula was then optimized to include 40.4% wheat straw, 20.3% corn straw, 18.3% soybean straw, combined with 20.0% wheat bran, and 1.0% light CaCO3 (C/N 42.50). The biological efciency was 15.2% greater than that of the control. Most encouraging was the indication= that the high yield comprehensive formula may shorten the time to reach the reproductive stage by 6 days, compared with the control. -
Why Mushrooms Have Evolved to Be So Promiscuous: Insights from Evolutionary and Ecological Patterns
fungal biology reviews 29 (2015) 167e178 journal homepage: www.elsevier.com/locate/fbr Review Why mushrooms have evolved to be so promiscuous: Insights from evolutionary and ecological patterns Timothy Y. JAMES* Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, MI 48109, USA article info abstract Article history: Agaricomycetes, the mushrooms, are considered to have a promiscuous mating system, Received 27 May 2015 because most populations have a large number of mating types. This diversity of mating Received in revised form types ensures a high outcrossing efficiency, the probability of encountering a compatible 17 October 2015 mate when mating at random, because nearly every homokaryotic genotype is compatible Accepted 23 October 2015 with every other. Here I summarize the data from mating type surveys and genetic analysis of mating type loci and ask what evolutionary and ecological factors have promoted pro- Keywords: miscuity. Outcrossing efficiency is equally high in both bipolar and tetrapolar species Genomic conflict with a median value of 0.967 in Agaricomycetes. The sessile nature of the homokaryotic Homeodomain mycelium coupled with frequent long distance dispersal could account for selection favor- Outbreeding potential ing a high outcrossing efficiency as opportunities for choosing mates may be minimal. Pheromone receptor Consistent with a role of mating type in mediating cytoplasmic-nuclear genomic conflict, Agaricomycetes have evolved away from a haploid yeast phase towards hyphal fusions that display reciprocal nuclear migration after mating rather than cytoplasmic fusion. Importantly, the evolution of this mating behavior is precisely timed with the onset of diversification of mating type alleles at the pheromone/receptor mating type loci that are known to control reciprocal nuclear migration during mating. -
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. -
Thèse De Doctorat
AIX-MARSEILLE UNIVERSITÉ Ecole Doctorale Sciences de la Vie et de la Santé THÈSE DE DOCTORAT Spécialité: Génétique Presenté par: Le HE Pour obtenir le grade de docteur de l’Université Aix-Marseille Interactions hôte-pathogène entre Caenorhabditis elegans et le champignon Drechmeria coniospora Soutenue le 2 décembre 2016 devant le jury composé de: Dr. Dominique Ferrandon Rapporteur Dr. Hinrich Schulenburg Rapporteur Dr. Philippe Naquet Président Dr. Eric Record Invité Dr. Jonathan Ewbank Directeur de thèse I TABLE OF CONTENTS Table of Figures ................................................................................................................ IV Table of Tables .................................................................................................................. V CHAPTER 1. Introduction............................................................................................ 1 1.1 Host-pathogen interactions ................................................................................... 1 1.1.1 C. elegans and its innate immunity ............................................................... 1 1.1.2 Nematophagous fungus ................................................................................. 5 1.1.3 Plant pathogenic fungi ................................................................................ 10 1.2 Fungal genetic modification ............................................................................... 17 1.2.1 Small RNA for Cross-species gene silencing ............................................ -
Field Guide to Common Macrofungi in Eastern Forests and Their Ecosystem Functions
United States Department of Field Guide to Agriculture Common Macrofungi Forest Service in Eastern Forests Northern Research Station and Their Ecosystem General Technical Report NRS-79 Functions Michael E. Ostry Neil A. Anderson Joseph G. O’Brien Cover Photos Front: Morel, Morchella esculenta. Photo by Neil A. Anderson, University of Minnesota. Back: Bear’s Head Tooth, Hericium coralloides. Photo by Michael E. Ostry, U.S. Forest Service. The Authors MICHAEL E. OSTRY, research plant pathologist, U.S. Forest Service, Northern Research Station, St. Paul, MN NEIL A. ANDERSON, professor emeritus, University of Minnesota, Department of Plant Pathology, St. Paul, MN JOSEPH G. O’BRIEN, plant pathologist, U.S. Forest Service, Forest Health Protection, St. Paul, MN Manuscript received for publication 23 April 2010 Published by: For additional copies: U.S. FOREST SERVICE U.S. Forest Service 11 CAMPUS BLVD SUITE 200 Publications Distribution NEWTOWN SQUARE PA 19073 359 Main Road Delaware, OH 43015-8640 April 2011 Fax: (740)368-0152 Visit our homepage at: http://www.nrs.fs.fed.us/ CONTENTS Introduction: About this Guide 1 Mushroom Basics 2 Aspen-Birch Ecosystem Mycorrhizal On the ground associated with tree roots Fly Agaric Amanita muscaria 8 Destroying Angel Amanita virosa, A. verna, A. bisporigera 9 The Omnipresent Laccaria Laccaria bicolor 10 Aspen Bolete Leccinum aurantiacum, L. insigne 11 Birch Bolete Leccinum scabrum 12 Saprophytic Litter and Wood Decay On wood Oyster Mushroom Pleurotus populinus (P. ostreatus) 13 Artist’s Conk Ganoderma applanatum -
Lacrymaria Lacrymabunda Lacrymaria
© Demetrio Merino Alcántara [email protected] Condiciones de uso Lacrymaria lacrymabunda (Bull.) Pat., Hyménomyc. Eur. (Paris): 123 (1887) Psathyrellaceae, Agaricales, Agaricomycetidae, Agaricomycetes, Agaricomycotina, Basidiomycota, Fungi = Agaricus areolatus Klotzsch, in Smith, Engl. Fl., Fungi (Edn 2) (London) 5(2): 112 (1836) = Agaricus areolatus Klotzsch, in Smith, Engl. Fl., Fungi (Edn 2) (London) 5(2): 112 (1836) var. areolatus ≡ Agaricus lacrymabundus Bull., Herb. Fr. (Paris) 5: tab. 194 (1785) ≡ Agaricus lacrymabundus Bull., Herb. Fr. (Paris) 5: tab. 194 (1785) var. lacrymabundus ≡ Agaricus lacrymabundus var. velutinus (Pers.) Fr., Syst. mycol. (Lundae) 1: 288 (1821) ≡ Agaricus lacrymabundus ß velutinus (Pers.) Fr., Syst. mycol. (Lundae) 1: 288 (1821) = Agaricus macrourus Pers., in Hoffmann, Naturgetr. Abbild. Beschr. Schwämme (Prague) 3 (1793) = Agaricus velutinus Pers., Syn. meth. fung. (Göttingen) 2: 409 (1801) = Agaricus velutinus var. macrourus (Pers.) Pers., Syn. meth. fung. (Göttingen) 2: 410 (1801) = Coprinus velutinus (Pers.) Gray, Nat. Arr. Brit. Pl. (London) 1: 633 (1821) = Drosophila velutina (Pers.) Kühner & Romagn., Fl. Analyt. Champ. Supér. (Paris): 371 (1953) ≡ Geophila lacrymabunda (Bull.) Quél., Enchir. fung. (Paris): 113 (1886) ≡ Geophila lacrymabunda (Bull.) Quél., Enchir. fung. (Paris): 113 (1886) var. lacrymabunda = Hypholoma aggregatum Peck, Ann. Rep. Reg. N.Y. St. Mus. 46: 28 (1894) [1893] = Hypholoma boughtoni Peck, Bull. N.Y. St. Mus. 139: 23 (1910) ≡ Hypholoma lacrymabundum (Bull.) Sacc. [as 'lacrimabundum'], Syll. fung. (Abellini) 5: 1033 (1887) = Hypholoma velutinum (Pers.) P. Kumm., Führ. Pilzk. (Zerbst): 72 (1871) ≡ Lacrymaria lacrymabunda f. gracillima J.E. Lange, Fl. Agaric. Danic. 4: 72 (1939) ≡ Lacrymaria lacrymabunda (Bull.) Pat., Hyménomyc. Eur. (Paris): 123 (1887) f. lacrymabunda ≡ Lacrymaria lacrymabunda (Bull.) Pat., Hyménomyc. Eur. -
Antioxidant Properties of Some Edible Fungi in the Genus Pleurotus
University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Masters Theses Graduate School 8-2005 Antioxidant Properties of Some Edible Fungi in The Genus Pleurotus Sharon Rose Jean-Philippe University of Tennessee - Knoxville Follow this and additional works at: https://trace.tennessee.edu/utk_gradthes Part of the Life Sciences Commons Recommended Citation Jean-Philippe, Sharon Rose, "Antioxidant Properties of Some Edible Fungi in The Genus Pleurotus. " Master's Thesis, University of Tennessee, 2005. https://trace.tennessee.edu/utk_gradthes/2093 This Thesis is brought to you for free and open access by the Graduate School at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Masters Theses by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. To the Graduate Council: I am submitting herewith a thesis written by Sharon Rose Jean-Philippe entitled "Antioxidant Properties of Some Edible Fungi in The Genus Pleurotus." I have examined the final electronic copy of this thesis for form and content and recommend that it be accepted in partial fulfillment of the requirements for the degree of Master of Science, with a major in Botany. Karen Hughes, Major Professor We have read this thesis and recommend its acceptance: Beth Mullin, Jay Whelan Accepted for the Council: Carolyn R. Hodges Vice Provost and Dean of the Graduate School (Original signatures are on file with official studentecor r ds.) To the Graduate Council: I am submitting herewith a thesis written by Sharon Rose Jean-Philippe entitled “Antioxidant properties of Some Edible Fungi in The Genus Pleurotus.” I have examined the final electronic copy of this thesis for form and content and recommend that it be accepted in partial fulfillment of the requirements for the degree of Master of Science, with a major in Botany. -
Fruiting Body Form, Not Nutritional Mode, Is the Major Driver of Diversification in Mushroom-Forming Fungi
Fruiting body form, not nutritional mode, is the major driver of diversification in mushroom-forming fungi Marisol Sánchez-Garcíaa,b, Martin Rybergc, Faheema Kalsoom Khanc, Torda Vargad, László G. Nagyd, and David S. Hibbetta,1 aBiology Department, Clark University, Worcester, MA 01610; bUppsala Biocentre, Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, SE-75005 Uppsala, Sweden; cDepartment of Organismal Biology, Evolutionary Biology Centre, Uppsala University, 752 36 Uppsala, Sweden; and dSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Center, 6726 Szeged, Hungary Edited by David M. Hillis, The University of Texas at Austin, Austin, TX, and approved October 16, 2020 (received for review December 22, 2019) With ∼36,000 described species, Agaricomycetes are among the and the evolution of enclosed spore-bearing structures. It has most successful groups of Fungi. Agaricomycetes display great di- been hypothesized that the loss of ballistospory is irreversible versity in fruiting body forms and nutritional modes. Most have because it involves a complex suite of anatomical features gen- pileate-stipitate fruiting bodies (with a cap and stalk), but the erating a “surface tension catapult” (8, 11). The effect of gas- group also contains crust-like resupinate fungi, polypores, coral teroid fruiting body forms on diversification rates has been fungi, and gasteroid forms (e.g., puffballs and stinkhorns). Some assessed in Sclerodermatineae, Boletales, Phallomycetidae, and Agaricomycetes enter into ectomycorrhizal symbioses with plants, Lycoperdaceae, where it was found that lineages with this type of while others are decayers (saprotrophs) or pathogens. We constructed morphology have diversified at higher rates than nongasteroid a megaphylogeny of 8,400 species and used it to test the following lineages (12). -
New Species and New Records of Clavariaceae (Agaricales) from Brazil
Phytotaxa 253 (1): 001–026 ISSN 1179-3155 (print edition) http://www.mapress.com/j/pt/ PHYTOTAXA Copyright © 2016 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.253.1.1 New species and new records of Clavariaceae (Agaricales) from Brazil ARIADNE N. M. FURTADO1*, PABLO P. DANIËLS2 & MARIA ALICE NEVES1 1Laboratório de Micologia−MICOLAB, PPG-FAP, Departamento de Botânica, Universidade Federal de Santa Catarina, Florianópolis, Brazil. 2Department of Botany, Ecology and Plant Physiology, Ed. Celestino Mutis, 3a pta. Campus Rabanales, University of Córdoba. 14071 Córdoba, Spain. *Corresponding author: Email: [email protected] Phone: +55 83 996110326 ABSTRACT Fourteen species in three genera of Clavariaceae from the Atlantic Forest of Brazil are described (six Clavaria, seven Cla- vulinopsis and one Ramariopsis). Clavaria diverticulata, Clavulinopsis dimorphica and Clavulinopsis imperata are new species, and Clavaria gibbsiae, Clavaria fumosa and Clavulinopsis helvola are reported for the first time for the country. Illustrations of the basidiomata and the microstructures are provided for all taxa, as well as SEM images of ornamented basidiospores which occur in Clavulinopsis helvola and Ramariopsis kunzei. A key to the Clavariaceae of Brazil is also included. Key words: clavarioid; morphology; taxonomy Introduction Clavariaceae Chevall. (Agaricales) comprises species with various types of basidiomata, including clavate, coralloid, resupinate, pendant-hydnoid and hygrophoroid forms (Hibbett & Thorn 2001, Birkebak et al. 2013). The family was first proposed to accommodate mostly saprophytic club and coral-like fungi that were previously placed in Clavaria Vaill. ex. L., including species that are now in other genera and families, such as Clavulina J.Schröt. -
Olympic Mushrooms 4/16/2021 Susan Mcdougall
Olympic Mushrooms 4/16/2021 Susan McDougall With links to species’ pages 206 species Family Scientific Name Common Name Agaricaceae Agaricus augustus Giant agaricus Agaricaceae Agaricus hondensis Felt-ringed Agaricus Agaricaceae Agaricus silvicola Forest Agaric Agaricaceae Chlorophyllum brunneum Shaggy Parasol Agaricaceae Chlorophyllum olivieri Olive Shaggy Parasol Agaricaceae Coprinus comatus Shaggy inkcap Agaricaceae Crucibulum laeve Common bird’s nest fungus Agaricaceae Cyathus striatus Fluted bird’s nest Agaricaceae Cystoderma amianthinum Pure Cystoderma Agaricaceae Cystoderma cf. gruberinum Agaricaceae Gymnopus acervatus Clustered Collybia Agaricaceae Gymnopus dryophilus Common Collybia Agaricaceae Gymnopus luxurians Agaricaceae Gymnopus peronatus Wood woolly-foot Agaricaceae Lepiota clypeolaria Shield dapperling Agaricaceae Lepiota magnispora Yellowfoot dapperling Agaricaceae Leucoagaricus leucothites White dapperling Agaricaceae Leucoagaricus rubrotinctus Red-eyed parasol Agaricaceae Morganella pyriformis Warted puffball Agaricaceae Nidula candida Jellied bird’s-nest fungus Agaricaceae Nidularia farcta Albatrellaceae Albatrellus avellaneus Amanitaceae Amanita augusta Yellow-veiled amanita Amanitaceae Amanita calyptroderma Ballen’s American Caesar Amanitaceae Amanita muscaria Fly agaric Amanitaceae Amanita pantheriana Panther cap Amanitaceae Amanita vaginata Grisette Auriscalpiaceae Lentinellus ursinus Bear lentinellus Bankeraceae Hydnellum aurantiacum Orange spine Bankeraceae Hydnellum complectipes Bankeraceae Hydnellum suaveolens