Handbook to Additional Fungal Species of Special Concern in the Northwest Forest Plan
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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. -
Appendix K. Survey and Manage Species Persistence Evaluation
Appendix K. Survey and Manage Species Persistence Evaluation Establishment of the 95-foot wide construction corridor and TEWAs would likely remove individuals of H. caeruleus and modify microclimate conditions around individuals that are not removed. The removal of forests and host trees and disturbance to soil could negatively affect H. caeruleus in adjacent areas by removing its habitat, disturbing the roots of host trees, and affecting its mycorrhizal association with the trees, potentially affecting site persistence. Restored portions of the corridor and TEWAs would be dominated by early seral vegetation for approximately 30 years, which would result in long-term changes to habitat conditions. A 30-foot wide portion of the corridor would be maintained in low-growing vegetation for pipeline maintenance and would not provide habitat for the species during the life of the project. Hygrophorus caeruleus is not likely to persist at one of the sites in the project area because of the extent of impacts and the proximity of the recorded observation to the corridor. Hygrophorus caeruleus is likely to persist at the remaining three sites in the project area (MP 168.8 and MP 172.4 (north), and MP 172.5-172.7) because the majority of observations within the sites are more than 90 feet from the corridor, where direct effects are not anticipated and indirect effects are unlikely. The site at MP 168.8 is in a forested area on an east-facing slope, and a paved road occurs through the southeast part of the site. Four out of five observations are more than 90 feet southwest of the corridor and are not likely to be directly or indirectly affected by the PCGP Project based on the distance from the corridor, extent of forests surrounding the observations, and proximity to an existing open corridor (the road), indicating the species is likely resilient to edge- related effects at the site. -
Mycena Sect. Galactopoda: Two New Species, a Key to the Known Species and a Note on the Circumscription of the Section
Mycosphere 4 (4): 653–659 (2013) ISSN 2077 7019 www.mycosphere.org Article Mycosphere Copyright © 2013 Online Edition Doi 10.5943/mycosphere/4/4/1 Mycena sect. Galactopoda: two new species, a key to the known species and a note on the circumscription of the section Aravindakshan DM and Manimohan P* Department of Botany, University of Calicut, Kerala, 673 635, India Aravindakshan DM, Manimohan P 2013 – Mycena sect. Galactopoda: two new species, a key to the known species and a note on the circumscription of the section. Mycosphere 4(4), 653–659, Doi 10.5943/mycosphere/4/4/1 Abstract Mycena lohitha sp. nov. and M. babruka sp. nov. are described from Kerala State, India and are assigned to sect. Galactopoda. Comprehensive descriptions, photographs, and comparisons with phenetically similar species are provided. A key is provided that differentiates all known species of the sect. Galactopoda. The circumscription of the section needs to be expanded to include some of the species presently assigned to it including the new species described here and a provisional, expanded circumscription of the section is followed in this paper. Key words – Agaricales – Basidiomycota – biodiversity – Mycenaceae – taxonomy Introduction Section Galactopoda (Earle) Maas Geest. of the genus Mycena (Pers.) Roussel (Mycenaceae, Agaricales, Basidiomycota) comprises species with medium-sized basidiomata with stipes that often exude a fluid when cut, exhibit coarse whitish fibrils at the base, and turn blackish when dried. Additionally they have ellipsoid and amyloid basidiospores, cheilocystidia that are generally fusiform and often with coloured contents, and hyphae of the pileipellis and stipitipellis covered with excrescences and diverticulate side branches. -
Introduction to Mycology
INTRODUCTION TO MYCOLOGY The term "mycology" is derived from Greek word "mykes" meaning mushroom. Therefore mycology is the study of fungi. The ability of fungi to invade plant and animal tissue was observed in early 19th century but the first documented animal infection by any fungus was made by Bassi, who in 1835 studied the muscardine disease of silkworm and proved the that the infection was caused by a fungus Beauveria bassiana. In 1910 Raymond Sabouraud published his book Les Teignes, which was a comprehensive study of dermatophytic fungi. He is also regarded as father of medical mycology. Importance of fungi: Fungi inhabit almost every niche in the environment and humans are exposed to these organisms in various fields of life. Beneficial Effects of Fungi: 1. Decomposition - nutrient and carbon recycling. 2. Biosynthetic factories. The fermentation property is used for the industrial production of alcohols, fats, citric, oxalic and gluconic acids. 3. Important sources of antibiotics, such as Penicillin. 4. Model organisms for biochemical and genetic studies. Eg: Neurospora crassa 5. Saccharomyces cerviciae is extensively used in recombinant DNA technology, which includes the Hepatitis B Vaccine. 6. Some fungi are edible (mushrooms). 7. Yeasts provide nutritional supplements such as vitamins and cofactors. 8. Penicillium is used to flavour Roquefort and Camembert cheeses. 9. Ergot produced by Claviceps purpurea contains medically important alkaloids that help in inducing uterine contractions, controlling bleeding and treating migraine. 10. Fungi (Leptolegnia caudate and Aphanomyces laevis) are used to trap mosquito larvae in paddy fields and thus help in malaria control. Harmful Effects of Fungi: 1. -
Peziza and Pezizaceae Inferred from Multiple Nuclear Genes: RPB2, -Tubulin, and LSU Rdna
Molecular Phylogenetics and Evolution 36 (2005) 1–23 www.elsevier.com/locate/ympev Evolutionary relationships of the cup-fungus genus Peziza and Pezizaceae inferred from multiple nuclear genes: RPB2, -tubulin, and LSU rDNA Karen Hansen ¤, Katherine F. LoBuglio, Donald H. PWster Harvard University Herbaria, Cambridge, MA 02138, USA Received 5 May 2004; revised 17 December 2004 Available online 22 April 2005 Abstract To provide a robust phylogeny of Pezizaceae, partial sequences from two nuclear protein-coding genes, RPB2 (encoding the sec- ond largest subunit of RNA polymerase II) and -tubulin, were obtained from 69 and 72 specimens, respectively, to analyze with nuclear ribosomal large subunit RNA gene sequences (LSU). The three-gene data set includes 32 species of Peziza, and 27 species from nine additional epigeous and six hypogeous (truZe) pezizaceous genera. Analyses of the combined LSU, RPB2, and -tubulin data set using parsimony, maximum likelihood, and Bayesian approaches identify 14 Wne-scale lineages within Pezizaceae. Species of Peziza occur in eight of the lineages, spread among other genera of the family, conWrming the non-monophyly of the genus. Although parsimony analyses of the three-gene data set produced a nearly completely resolved strict consensus tree, with increased conWdence, relationships between the lineages are still resolved with mostly weak bootstrap support. Bayesian analyses of the three- gene data, however, show support for several more inclusive clades, mostly congruent with Bayesian analyses of RPB2. No strongly supported incongruence was found among phylogenies derived from the separate LSU, RPB2, and -tubulin data sets. The RPB2 region appeared to be the most informative single gene region based on resolution and clade support, and accounts for the greatest number of potentially parsimony informative characters within the combined data set, followed by the LSU and the -tubulin region. -
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 -
Chapter 5 Conidiophore Initiation and Conidiogenesis 5.1
102 Chapter 5 Conidiophore initiation and conidiogenesis 5.1 INTRODUCTION In this chapter are described the processes of conidiophore initiation and conidiogenesis in some Australian cercosporoid fungi. The involvement of wall layers of the conidiophore mother cell in conidiophore initiation is examined, and the events involved in conidiogenesis are then considered in terms of the following successive developmental steps proposed by Minter et al. (1982). (a) Conidiophore initiation. Ultrastructural studies showed that the production of conidiophores from stroma cells in Cercospora beticola can be enteroblastic or holoblastic (Pons et al., 1985). In enteroblastic initiation, the outer, opaque layer of the conidiophore wall was continuous with the middle wall layer of the stroma cell. The outer layer of the generative cell either stopped abruptly or else merged imperceptibly with the wall of the conidiophore. The latter type of conidiophore initiation resembled that from vegetative hyphae in Pleiochaeta setosa (Kirchn.) Hughes (Harvey, 1974). (b) Conidium ontogeny, described as 'the ways in which conidial cell walls are produced' (Minter et al., 1982). The accepted view that conidium initiation is holoblastic in the cercosporoid fungi (Ellis, 1971) was supported by the results of Pons et al. (1985). (c) Conidium delimitation, described as 'the ways in which delimiting septa are produced' (Minter et al., 1982). Every conidium is delimited by a septum prior to abscission, but the exact structure of the septum, the stage of development at which it is formed (relative to the stage of expansion of the conidium) and the timing of the plugging of the septal pore by Woronin bodies (which interrupt its cytoplasmic connection with the conidiogenous cell) can vary. -
Russulas of Southern Vancouver Island Coastal Forests
Russulas of Southern Vancouver Island Coastal Forests Volume 1 by Christine Roberts B.Sc. University of Lancaster, 1991 M.S. Oregon State University, 1994 A Dissertation Submitted in Partial Fulfillment of the Requirements for the Degree of DOCTOR OF PHILOSOPHY in the Department of Biology © Christine Roberts 2007 University of Victoria All rights reserved. This dissertation may not be reproduced in whole or in part, by photocopying or other means, without the permission of the author. Library and Bibliotheque et 1*1 Archives Canada Archives Canada Published Heritage Direction du Branch Patrimoine de I'edition 395 Wellington Street 395, rue Wellington Ottawa ON K1A0N4 Ottawa ON K1A0N4 Canada Canada Your file Votre reference ISBN: 978-0-494-47323-8 Our file Notre reference ISBN: 978-0-494-47323-8 NOTICE: AVIS: The author has granted a non L'auteur a accorde une licence non exclusive exclusive license allowing Library permettant a la Bibliotheque et Archives and Archives Canada to reproduce, Canada de reproduire, publier, archiver, publish, archive, preserve, conserve, sauvegarder, conserver, transmettre au public communicate to the public by par telecommunication ou par Plntemet, prefer, telecommunication or on the Internet, distribuer et vendre des theses partout dans loan, distribute and sell theses le monde, a des fins commerciales ou autres, worldwide, for commercial or non sur support microforme, papier, electronique commercial purposes, in microform, et/ou autres formats. paper, electronic and/or any other formats. The author retains copyright L'auteur conserve la propriete du droit d'auteur ownership and moral rights in et des droits moraux qui protege cette these. -
Wood Decay Fungi in Landscape Trees
Pest Notes, Publication 74109 Revised August 2019 Integrated Pest Management for Home Gardeners and Landscape Professionals Wood Decay Fungi in Landscape Trees everal fungal diseases, sometimes called heart rots, Ssap rots, or canker rots, decay wood in tree trunks Figure 1. White rot of oak. and limbs (Figures 1 and 2). Under conditions favor- ing growth of specific rot fungi, extensive portions of the wood of living trees can decay in a relatively short time (i.e., months to years). Decay fungi reduce wood strength and may kill storage and conductive tissues in the sapwood. While most species of woody plants are subject to trunk and limb decay, older and weaker trees are most susceptible. DAMAGE Decay fungi destroy cell wall components; including cellulose, hemicellulose, and lignin, that make up the woody portion of a tree. Depending on the organism, decay fungi can destroy the living (sapwood) or the central core (heartwood) part of the tree. Decay isn’t always visible on the outside of the tree, except where the bark Figure 2. Heart brown rot in a conifer trunk. has been cut or injured, when a cavity is present, or when rot fungi produce reproductive structures. Wood decay can make trees hazardous, of wood weight can result in 70 to 90% as infected trunks and limbs become loss in wood strength. Many branches unable to support their own weight and that fall from trees appear sound, but fall, especially when stressed by wind, upon analysis, they were colonized by Authors: heavy rain, or other conditions. Decay wood decay organisms. -
Heavy Metal Remediation: Transport and Accumulation in Plants
ENVIRONMENTAL RESEARCH ADVANCES HEAVY METAL REMEDIATION TRANSPORT AND ACCUMULATION IN PLANTS No part of this digital document may be reproduced, stored in a retrieval system or transmitted in any form or by any means. The publisher has taken reasonable care in the preparation of this digital document, but makes no expressed or implied warranty of any kind and assumes no responsibility for any errors or omissions. No liability is assumed for incidental or consequential damages in connection with or arising out of information contained herein. This digital document is sold with the clear understanding that the publisher is not engaged in rendering legal, medical or any other professional services. ENVIRONMENTAL RESEARCH ADVANCES Additional books in this series can be found on Nova‘s website under the Series tab. Additional e-books in this series can be found on Nova‘s website under the e-book tab. ENVIRONMENTAL RESEARCH ADVANCES HEAVY METAL REMEDIATION TRANSPORT AND ACCUMULATION IN PLANTS DHARMENDRA KUMAR GUPTA AND SOUMYA CHATTERJEE EDITORS New York Copyright © 2014 by Nova Science Publishers, Inc. All rights reserved. No part of this book may be reproduced, stored in a retrieval system or transmitted in any form or by any means: electronic, electrostatic, magnetic, tape, mechanical photocopying, recording or otherwise without the written permission of the Publisher. For permission to use material from this book please contact us: Telephone 631-231-7269; Fax 631-231-8175 Web Site: http://www.novapublishers.com NOTICE TO THE READER The Publisher has taken reasonable care in the preparation of this book, but makes no expressed or implied warranty of any kind and assumes no responsibility for any errors or omissions. -
Sporocarp Ontogeny in Panus (Basidiomycotina): Evolution and Classification
Sporocarp Ontogeny in Panus (Basidiomycotina): Evolution and Classification David S. Hibbett; Shigeyuki Murakami; Akihiko Tsuneda American Journal of Botany, Vol. 80, No. 11. (Nov., 1993), pp. 1336-1348. Stable URL: http://links.jstor.org/sici?sici=0002-9122%28199311%2980%3A11%3C1336%3ASOIP%28E%3E2.0.CO%3B2-M American Journal of Botany is currently published by Botanical Society of America. Your use of the JSTOR archive indicates your acceptance of JSTOR's Terms and Conditions of Use, available at http://www.jstor.org/about/terms.html. JSTOR's Terms and Conditions of Use provides, in part, that unless you have obtained prior permission, you may not download an entire issue of a journal or multiple copies of articles, and you may use content in the JSTOR archive only for your personal, non-commercial use. Please contact the publisher regarding any further use of this work. Publisher contact information may be obtained at http://www.jstor.org/journals/botsam.html. Each copy of any part of a JSTOR transmission must contain the same copyright notice that appears on the screen or printed page of such transmission. The JSTOR Archive is a trusted digital repository providing for long-term preservation and access to leading academic journals and scholarly literature from around the world. The Archive is supported by libraries, scholarly societies, publishers, and foundations. It is an initiative of JSTOR, a not-for-profit organization with a mission to help the scholarly community take advantage of advances in technology. For more information regarding JSTOR, please contact [email protected]. http://www.jstor.org Tue Jan 8 09:54:21 2008 American Journal of Botany 80(11): 1336-1348. -
Escovopsis Trichodermoides Sp. Nov., Isolated from a Nest of the Lower Attine Ant Mycocepurus Goeldii
Antonie van Leeuwenhoek (2015) 107:731–740 DOI 10.1007/s10482-014-0367-1 ORIGINAL PAPER Escovopsis trichodermoides sp. nov., isolated from a nest of the lower attine ant Mycocepurus goeldii Virginia E. Masiulionis • Marta N. Cabello • Keith A. Seifert • Andre Rodrigues • Fernando C. Pagnocca Received: 30 April 2014 / Accepted: 18 December 2014 / Published online: 10 January 2015 Ó Springer International Publishing Switzerland 2015 Abstract Currently, five species are formally other species by highly branched, trichoderma-like described in Escovopsis, a specialized mycoparasitic conidiophores lacking swollen vesicles, with reduced genus of fungus gardens of attine ants (Hymenoptera: conidiogenous cells and distinctive conidia morphol- Formicidae: tribe Attini). Four species were isolated ogy. Phylogenetic analyses based on partial tef1 gene from leaf-cutting ants in Brazil, including Escovopsis sequences support the distinctiveness of this species. moelleri and Escovopsis microspora from nests of A portion of the internal transcribed spacers of the Acromyrmex subterraneus molestans, Escovopsis nuclear rDNA was sequenced to serve as a DNA weberi from a nest of Atta sp. and Escovopsis barcode. Future molecular and morphological studies lentecrescens from a nest of Acromyrmex subterran- in this group of fungi will certainly unravel the eus subterraneus. The fifth species, Escovopsis taxonomic diversity of Escovopsis associated with aspergilloides was isolated from a nest of the higher fungus-growing ants. attine ant Trachymyrmex ruthae from Trinidad. Here, we describe a new species, Escovopsis trichodermo- Keywords Attini Á Fungus-growing ant Á ides isolated from a fungus garden of the lower attine Hypocreales Á Mycoparasitism ant Mycocepurus goeldii, which differs from the five V.