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Chorioactidaceae: a New Family in the Pezizales (Ascomycota) with Four Genera
mycological research 112 (2008) 513–527 journal homepage: www.elsevier.com/locate/mycres Chorioactidaceae: a new family in the Pezizales (Ascomycota) with four genera Donald H. PFISTER*, Caroline SLATER, Karen HANSENy Harvard University Herbaria – Farlow Herbarium of Cryptogamic Botany, Department of Organismic and Evolutionary Biology, Harvard University, 22 Divinity Avenue, Cambridge, MA 02138, USA article info abstract Article history: Molecular phylogenetic and comparative morphological studies provide evidence for the Received 15 June 2007 recognition of a new family, Chorioactidaceae, in the Pezizales. Four genera are placed in Received in revised form the family: Chorioactis, Desmazierella, Neournula, and Wolfina. Based on parsimony, like- 1 November 2007 lihood, and Bayesian analyses of LSU, SSU, and RPB2 sequence data, Chorioactidaceae repre- Accepted 29 November 2007 sents a sister clade to the Sarcosomataceae, to which some of these taxa were previously Corresponding Editor: referred. Morphologically these genera are similar in pigmentation, excipular construction, H. Thorsten Lumbsch and asci, which mostly have terminal opercula and rounded, sometimes forked, bases without croziers. Ascospores have cyanophilic walls or cyanophilic surface ornamentation Keywords: in the form of ridges or warts. So far as is known the ascospores and the cells of the LSU paraphyses of all species are multinucleate. The six species recognized in these four genera RPB2 all have limited geographical distributions in the northern hemisphere. Sarcoscyphaceae ª 2007 The British Mycological Society. Published by Elsevier Ltd. All rights reserved. Sarcosomataceae SSU Introduction indicated a relationship of these taxa to the Sarcosomataceae and discussed the group as the Chorioactis clade. Only six spe- The Pezizales, operculate cup-fungi, have been put on rela- cies are assigned to these genera, most of which are infre- tively stable phylogenetic footing as summarized by Hansen quently collected. -
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. -
The Ascomycota
Papers and Proceedings of the Royal Society of Tasmania, Volume 139, 2005 49 A PRELIMINARY CENSUS OF THE MACROFUNGI OF MT WELLINGTON, TASMANIA – THE ASCOMYCOTA by Genevieve M. Gates and David A. Ratkowsky (with one appendix) Gates, G. M. & Ratkowsky, D. A. 2005 (16:xii): A preliminary census of the macrofungi of Mt Wellington, Tasmania – the Ascomycota. Papers and Proceedings of the Royal Society of Tasmania 139: 49–52. ISSN 0080-4703. School of Plant Science, University of Tasmania, Private Bag 55, Hobart, Tasmania 7001, Australia (GMG*); School of Agricultural Science, University of Tasmania, Private Bag 54, Hobart, Tasmania 7001, Australia (DAR). *Author for correspondence. This work continues the process of documenting the macrofungi of Mt Wellington. Two earlier publications were concerned with the gilled and non-gilled Basidiomycota, respectively, excluding the sequestrate species. The present work deals with the non-sequestrate Ascomycota, of which 42 species were found on Mt Wellington. Key Words: Macrofungi, Mt Wellington (Tasmania), Ascomycota, cup fungi, disc fungi. INTRODUCTION For the purposes of this survey, all Ascomycota having a conspicuous fruiting body were considered, excluding Two earlier papers in the preliminary documentation of the endophytes. Material collected during forays was described macrofungi of Mt Wellington, Tasmania, were confined macroscopically shortly after collection, and examined to the ‘agarics’ (gilled fungi) and the non-gilled species, microscopically to obtain details such as the size of the -
Contribution to the Study of Neotropical Discomycetes: a New Species of the Genus Geodina (Geodina Salmonicolor Sp
Mycosphere 9(2): 169–177 (2018) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/9/2/1 Copyright © Guizhou Academy of Agricultural Sciences Contribution to the study of neotropical discomycetes: a new species of the genus Geodina (Geodina salmonicolor sp. nov.) from the Dominican Republic Angelini C1,2, Medardi G3, Alvarado P4 1 Jardín Botánico Nacional Dr. Rafael Ma. Moscoso, Santo Domingo, República Dominicana 2 Via Cappuccini 78/8, 33170 (Pordenone) 3 Via Giuseppe Mazzini 21, I-25086 Rezzato (Brescia) 4 ALVALAB, La Rochela 47, E-39012 Santander, Spain Angelini C, Medardi G, Alvarado P 2018 - Contribution to the study of neotropical discomycetes: a new species of the genus Geodina (Geodina salmonicolor sp. nov.) from the Dominican Republic. Mycosphere 9(2), 169–177, Doi 10.5943/mycosphere/9/2/1 Abstract Geodina salmonicolor sp. nov., a new neotropical / equatorial discomycetes of the genus Geodina, is here described and illustrated. The discovery of this new entity allowed us to propose another species of Geodina, until now a monospecific genus, and produce the first 28S rDNA genetic data, which supports this species is related to genus Wynnea in the Sarcoscyphaceae. Key-words – 1 new species – Ascomycota – Sarcoscyphaceae – Sub-tropical zone Caribbeans – Taxonomy Introduction A study started more than 10 years ago in the area of Santo Domingo (Dominican Republic) by one of the authors allowed us to identify several interesting fungal species, both Basidiomycota and Ascomycota. Angelini & Medardi (2012) published a first report of ascomycetes in which 12 lignicolous species including discomycetes and pyrenomycetes were described and illustrated in detail, also delineating the physical and botanical characteristics of the research area. -
Truffles and False Truffles: a Primer by Britt A
Two views of Tuber canaliculatum. Photos: John Plschke III. Truffles and False Truffles: A Primer by Britt A. Bunyard; photos by John Plischke III Nothing in biology makes sense except in the light of evolution. —Theodosius Dobzhansky (1900–1979) Truffles have been the stuff of legend and culinary delight for genus of the most highly prized species of truffles.) As with every- centuries, even millennia. Historically, all mushrooms have been thing in nature, though, there is a reason. regarded with mystery or suspicion due mostly to their habit of materializing overnight (completely unlike other “plants”) and Form follows function: the convoluted hymenium often in rings (which was clearly the work of dancing fairies). Truffles are curiouser still in that they develop entirely under- Although it may not be obvious upon first inspection, species of ground. Theophrastus (372–287 B.C.) is credited with the earli- truffle are most closely related to members of the order Pezizales, est authorship of the group; he considered them the strangest of which includes Peziza, the eyelash fungus (Scutellinia scutellata), all plants (you will recall that, until fairly recently, fungi were and the beautiful scarlet cup (Sarcoscypha coccinea). But how did classified as plants) because they lack any plantlike features, in- members of the genus Tuber and their relatives go from a flattened cluding roots. morphology and epigeous (above ground) growth habit to highly When we think of truffles, we hardly get an image of the convoluted and hypogeous (subterranean)? In his terrific book typical fungus fruitbody, much less that of a mushroom. Not The Fifth Kingdom, Bryce Kendrick illustrates the evolutionary classified with true mushrooms (the Basidiomycetes), the truffles sequence from a flattened, above-ground cup like Peziza that likely possess sac-like spore producing structures (the ascus; plural gave rise to fungi that were increasingly convoluted like Genea. -
Paper Format : Instruction to Authors
Proceedings of the 7th International Conference on Mushroom Biology and Mushroom Products (ICMBMP7) 2011 TAXONOMIC SIGNIFICANCE OF ANAMORPHIC CHARACTERISTICS IN THE LIFE CYCLE OF COPRINOID MUSHROOMS SUSANNA M. BADALYAN1, MÓNICA NAVARRO-GONZÁLEZ2, URSULA KÜES2 1Laboratory of Fungal Biology and Biotechnology, Faculty of Biology, Yerevan State University 1 Aleg Manoogian St., 0025, Yerevan Armenia 2Georg-August-Universität Göttingen, Büsgen-Institut, Molekulare Holzbiotechnologie und technische Mykologie Büsgenweg 2, 37077 Göttingen Germany [email protected] , [email protected] , [email protected] ABSTRACT Ink cap fungi (coprinoid mushrooms) are not monophyletic and divide into Coprinellus, Coprinopsis and Parasola (all Psathyrellaceae) and Coprinus (Agaricaceae). Knowledge on morphological mycelial features and asexual reproduction modes of coprini is restricted, with Coprinopsis cinerea being the best described species. This species produces constitutively on monokaryons and light-induced on dikaryons unicellular uninucleate haploid arthroconidia (oidia) on specific aerial structures (oidiophores). The anamorphic name Hormographiella aspergillata was coined for oidia production on monokaryons. Two other Hormographiella species are described in the literature, one unknown (candelabrata) and one (verticillata) identified as Coprinellus domesticus. Another, yet sterile anamorph associated with some coprini is called Ozonium which describes the incidence of tawny-rust mycelial mats of pigmented, well septated and clampless hyphal strands as -
Coprinellus, Coprinopsis, Parasola)
Andreas Melzer, Kyhnaer Hauptstraße 5, 04509 Wiedemar, Germany http://www.vielepilze.de/ Key to coprinoid species (Coprinellus, Coprinopsis, Parasola) Latest update: 04.04.17 09.11.15 (first version), 23.12.15 (part 3.4.: another sequence), 10.01.16 (Parasola cuniculorum added, another sequence in part 1.2.), 14.01.16 (Coprinopsis lagopides replaced by C. phlyctidospora), 21.03.16 (data and line drawing of Coprinopsis villosa changed), 23.04.16 (microcharacters of Parasola schroeteri corrrected), 08.05.16 (Coprinopsis maysoidispora intergrated in Picacei, another sequence in part 2.2.from 9, in part 3.1 from 16), 19.05.16 (Coprinopsis alcobae added, another sequence in part 3.1. from 16, Coprinopsis mexicana and Coprinus maculatus added, another sequence in part 3.4. from 23), 16.07.16 (Coprinellus aokii added, another sequence in part 2.5. from 21, Coprinopsis jamaicensis added, another sequence in part 3.4. from 41, C. austrofriesii, burkii, caribaea, clastophylla, depressiceps, fibrillosa, striata added, another sequence in part 3.1. from 22, C. caracasensis added, another sequence in part 3.3. from 17), 16.10.16 (C. phaeopunctata added in part 3.1 number 16, C. alcobae removed from there, added in part 3.1., number 30, another sequence in part 3.1. from 30), 22.11.16 (C. igarashi added in part 3.3., another another sequence in part 3.3. from 9), 04-04.17 (Coprinopsis aesontiensis aded in part 3.4. 47*, another sequence in part 3.4. from 45). Introduction: The key includes most of the previously described coprinoid species from Europe and many from other continents, in addition, some of which have since been transferred from the genera Psathyrella. -
Ascomycete Fungi Species List
Ascomycete Fungi Species List Higher Classification1 Kingdom: Fungi, Phylum: Ascomycota Class (C:), Order (O:) and Family (F:) Scientific Name1 English Name(s)2 C: Geoglossomycetes (Earth Tongues) O: Geoglossales F: Geoglossaceae Trichoglossum hirsutum Black Earth Tongue C: Leotiomycetes O: Helotiales F: Bulgariaceae Bulgaria inquinans Black Bulgar F: Helotiaceae Chlorociboria aeruginascens Green Elfcup, Green Wood Cup, Green Stain Fungus F: Leotiaceae Leotia lubrica Jellybaby F: Vibrisseaceae Vibrissea truncorum O: Pezizales F: Helvellaceae Gyromitra infula Hooded False Morel, Elfin Saddle Helvella macropus Felt Saddle Fungus Helvella spp. Elfin Saddles F: Pyronemataceae Cheilymenia theleboloides Scutellinia scutellata Eyelash Cup F: Sarcoscyphaceae Cookeina speciosa Cookeina venezuelae C: Sordariomycetes O: Hypocreales F: Clavicipitaceae Ophiocordyceps melolonthae O: Xylariales F: Xylariaceae Daldinia sp. Xylaria globosa Xylaria hypoxylon Candlestick Fungus, Candlesnuff Fungus, Stag's Horn Fungus Xylaria polymorpha Dead Man's Fingers Xylaria spp. Xylocoremium sp. Page 1 of 2 Cloudbridge Nature Reserve, Costa Rica Last Updated: February 3, 2017 Ascomycete Fungi Species List NOTES: Short-forms: sp. = one species of the given genus identified; spp. = more than one of species of the given genus identified 1, Classification and scientific names based on current classifications as found on MycoBank (www.mycobank.org) 2, English names are not standardized for fungi and the English names provided are not considered the definitive names for the given species. English names were gathered from a variety of sources including mushroom identification books and various fungi related websites. Contributors: Major Contributor – Baptiste Saunier. Other Contributors – Ranzeth Gómez Navarro. Page 2 of 2 Cloudbridge Nature Reserve, Costa Rica Last Updated: February 3, 2017 . -
Monstruosities Under the Inkap Mushrooms
Monstruosities under the Inkap Mushrooms M. Navarro-González*1; A. Domingo-Martínez1; S. S. Navarro-González1; P. Beutelmann2; U. Kües1 1. Molecular Wood Biotechnology, Institute of Forest Botany, Georg-August-University Göttingen, Büsgenweg 2, D-37077 Göttingen, Germany. 2. Institute of General Botany, Johannes Gutenberg-University of Mainz, Müllerweg 6, D-55099 Mainz, Germany Four different Inkcaps were isolated from horse dung and tested for growth on different medium. In addition to normal-shaped mushrooms, three of the isolates formed fruiting body-like structures re- sembling the anamorphs of Rhacophyllus lilaceus, a species originally believed to be asexual. Teleo- morphs of this species were later found and are known as Coprinus clastophyllus, respectively Coprinop- sis clastophylla. The fourth of our isolates also forms mushrooms but most of them are of crippled shape. Well-shaped umbrella-like mushrooms assigns this Inkcap to the clade Coprinellus. ITS se- quencing confirmed that the first three strains and the Rhacophyllus type strain belong to the genus Coprinopsis and that the fourth isolate belongs to the genus Coprinellus. 1. Introduction Inkcaps are a group of about 200 basidiomycetes whose mushrooms usually deliquesce shortly after maturation for spore liberation (see Fig. 1). Until re- cently, they were compiled under the one single genus Coprinus. However, molecular data divided this group into four new genera: Coprinus, Coprinop- sis, Coprinellus and Parasola (Redhead et al. 2001). Genetics and Cellular Biology of Basidiomycetes-VI. A.G. Pisabarro and L. Ramírez (eds.) © 2005 Universidad Pública de Navarra, Spain. ISBN 84-9769-107-5 113 FULL LENGTH CONTRIBUTIONS Figure 1. Mushrooms of Coprinopsis cinerea strain AmutBmut (about 12 cm in size) formed on horse dung, the natural substrate of the fungus. -
Fungi from the Owyhee Region
FUNGI FROM THE OWYHEE REGION OF SOUTHERN IDAHO AND EASTERN OREGON bY Marcia C. Wicklow-Howard and Julie Kaltenecker Boise State University Boise, Idaho Prepared for: Eastside Ecosystem Management Project October 1994 THE OWYHEE REGION The Owyhee Region is south of the Snake River and covers Owyhee County, Idaho, Malheur County, Oregon, and a part of northern Nevada. It extends approximately from 115” to 118” West longitude and is bounded by parallels 41” to 44”. Owyhee County includes 7,662 square miles, Malheur County has 9,861 square miles, and the part of northern Nevada which is in the Owyhee River watershed is about 2,900 square miles. The elevations in the region range from about 660 m in the Snake River Plains and adjoining Owyhee Uplands to 2522 m at Hayden Peak in the Owyhee Mountains. Where the Snake River Plain area is mostly sediment-covered basalt, the area south of the Snake River known as the Owyhee Uplands, includes rolling hills, sharply dissected by basaltic plateaus. The Owyhee Mountains have a complex geology, with steep slopes of both basalt and granite. In the northern areas of the Owyhee Mountains, the steep hills, mountains, and escarpments consist of basalt. In other areas of the mountains the steep slopes are of granitic or rhyolitic origin. The mountains are surrounded by broad expanses of sagebrush covered plateaus. The soils of the Snake River Plains are generally non-calcareous and alkaline. Most are well-drained, with common soil textures of silt loam, loam and fine sand loam. In the Uplands and Mountains, the soils are often coarse textured on the surface, while the subsoils are loamy and non-calcareous. -
DNA Barcoding Facilitates a Rapid Biotic Survey of a Temperate Nature
Biodiversity inventories in high gear: DNA barcoding facilitates a rapid biotic survey of a temperate nature reserve Angela Telfer, Monica Young, Jenna Quinn, Kate Perez, Crystal Sobel, Jayme Sones, Valerie Levesque-Beaudin, Rachael Derbyshire, Jose Fernandez-Triana, Rodolphe Rougerie, et al. To cite this version: Angela Telfer, Monica Young, Jenna Quinn, Kate Perez, Crystal Sobel, et al.. Biodiversity inven- tories in high gear: DNA barcoding facilitates a rapid biotic survey of a temperate nature reserve. Biodiversity Data Journal, Pensoft, 2015, 3, pp.e6313. 10.3897/BDJ.3.e6313. hal-01206879 HAL Id: hal-01206879 https://hal-univ-rennes1.archives-ouvertes.fr/hal-01206879 Submitted on 12 Oct 2015 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Biodiversity Data Journal 3: e6313 doi: 10.3897/BDJ.3.e6313 Taxonomic Paper Biodiversity inventories in high gear: DNA barcoding facilitates a rapid biotic survey of a temperate nature reserve Angela C Telfer‡, Monica R Young‡§, Jenna Quinn , Kate Perez‡, Crystal N Sobel‡, Jayme E Sones‡, Valerie Levesque-Beaudin‡, -
Western Pennsylvania Mushroom Club Newsletter ■ Fungi, Fun & Friends! ■
Western Pennsylvania Mushroom Club Newsletter ■ Fungi, Fun & Friends! ■ VOLUME 21, ISSUE 2 MAY / JUNE 2021 President’s Message 2021 Meeting Schedule STEPHEN BUCKLIN May 18 Tosca Terán and Andrei Gravelle Fungi Frequencies And we’re off! After six weeks of getting increasingly From the Midnight Mushroom Music archives to the My- more sunlight than darkness in our corrhizal Rhythm Machine to fungi-controlled VR experi- days, the soil has warmed significant- ences, Tosca Terán and Andrei Gravelle (the visionaries ly, and the woods around us are “waking up.” For most people of Nanotopia) construct soundscapes and installations with an inclination towards fungi, the seasonal changes we’re involving biodata-sonification of fungi. The duo will present experiencing mean only one thing is on the mind—morels! their past and upcoming projects and how they came to While the changes we associate with the emergence of mo- work intimately with fungi. They will also give a behind-the- rels—the unfurling of mayapples, the blooming of trilliums, the scenes look at their collaborative composition process that addition of songs from black-throated green warblers to the involves channeling the electrical energies of cultivated forest soundscape—are captivating in and of themselves, few fungi through synthesizers. things captivate mycophagists the way morel mushrooms do. June 15 Dr. Kristen Wickert When I joined the club in 2017, I was a novice forager in- terested in learning more about edible fungi I could find in Fungi as Plant Pathogens the woods of Western Pennsylvania. I had tried a generous Plant pathology is like a giant puzzle with many different friend’s sauteed morels and was hoping to learn more about pieces that tell a story about our ecosystem’s health.