Handbook to Strategy 1 Fungal Species in the Northwest Forest
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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. -
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. -
The Secotioid Syndrome
76(1) Mycologia January -February 1984 Official Publication of the Mycological Society of America THE SECOTIOID SYNDROME Department of Biological Sciences, Sun Francisco State University, Sun Francisco, California 94132 I would like to begin this lecture by complimenting the Officers and Council of The Mycological Society of America for their high degree of cooperation and support during my term of office and for their obvious dedication to the welfare of the Society. In addition. I welcome the privilege of expressing my sincere appreciation to the membership of The Mycological Society of America for al- lowing me to serve them as President and Secretary-Treasurer of the Society. It has been a long and rewarding association. Finally, it is with great pleasure and gratitude that I dedicate this lecture to Dr. Alexander H. Smith, Emeritus Professor of Botany at the University of Michigan, who, over thirty years ago in a moment of weakness, agreed to accept me as a graduate student and who has spent a good portion of the ensuing years patiently explaining to me the intricacies, inconsis- tencies and attributes of the higher fungi. Thank you, Alex, for the invaluable experience and privilege of spending so many delightful and profitable hours with you. The purpose of this lecture is to explore the possible relationships between the gill fungi and the secotioid fungi, both epigeous and hypogeous, and to present a hypothesis regarding the direction of their evolution. Earlier studies on the secotioid fungi have been made by Harkness (I), Zeller (13). Zeller and Dodge (14, 15), Singer (2), Smith (5. -
2021 Public Beach List
2021 Public Beach List - Special Rules The following is a list of popular public beaches with special rules because of resource needs and/or restrictions on harvest due to health concerns. If a beach is not listed below or on page 2, it is open for recreational harvest year-round unless closed by emergency rule, pollution or shellfish safety closures. Click for WDFW Public Beach webpages and seasons 2021 Beach Seasons adopted February 26, 2021 Open for Clams, Mussels & Oysters = Open for Oysters Only = For more information, click on beach name below to view Jan1- Jan15- Feb1- Feb15- Mar1- Mar15- Apr1- Apr15- May1- May15- Jun1- Jun15- Jul1- Jul15- Aug1- Aug15- Sep1- Sep15- Oct1- Oct15- Nov1- Nov15- Dec1- Dec15- beach-specific webpage. Jan15 Jan31 Feb15 Feb28 Mar15 Mar31 Apr15 Apr30 May15 May31 Jun15 Jun30 Jul15 Jul31 Aug15 Aug31 Sep15 Sep30 Oct15 Oct31 Nov15 Nov30 Dec15 Dec31 Ala Spit No natural production of oysters Belfair State Park Birch Bay State Park Dash Point State Park Dosewallips State Park Drayton West Duckabush Dungeness Spit/NWR Tidelands No natural production of oysters Eagle Creek Fort Flagler State Park Freeland County Park No natural production of oysters. Frye Cove County Park Hope Island State Park Illahee State Park Limited natural production of clams Indian Island County Park No natural production of oysters Kitsap Memorial State Park CLAMS AND OYSTERS CLOSED Kopachuck State Park Mystery Bay State Park Nahcotta Tidelands (Willapa Bay) North Bay Oak Bay County Park CLAMS AND OYSTERS CLOSED Penrose Point State Park Point -
BOTANICAL RESOURCES REPORT Chetco Wild and Scenic River Mineral Withdrawal Project Rogue River-Siskiyou National Forest Gold Beach Ranger District
BOTANICAL RESOURCES REPORT Chetco Wild and Scenic River Mineral Withdrawal Project Rogue River-Siskiyou National Forest Gold Beach Ranger District Clint Emerson District Botanist October 25, 2012 CONTENTS 1 Introduction ........................................................................................................................................... 2 2 Project and Effects Summary ................................................................................................................ 2 3 Affected Environment ........................................................................................................................... 2 3.1 Botanical Resources ...................................................................................................................... 3 3.1.1 Threatened, Endangered, Sensitive and survey and Manage Plant and Fungi Species 3 3.1.2 Invasive Plant Species ......................................................................................................... 6 4 Environmental Effects........................................................................................................................... 7 4.1 Effects on Botanical Resources ..................................................................................................... 8 4.1.1 Effects on Threatened, Endangered, Sensitive and Survey and Manage Plant and Fungi Species 8 4.1.2 Risk of Invasive Plant Species Spread .................................................................................. 9 References .................................................................................................................................................. -
State Park Contact Sheet Last Updated November 2016
WASHINGTON STATE PARKS AND RECREATION COMMISSION Film Permit Application State Park Contact Sheet Last Updated November 2016 AREA MANAGER PHONE PARK NAME PARK AREA ADDRESS EMAIL (@parks.wa.gov) REGION Sharon Soelter ALTA LAKE STATE PARK (509) 923-2473 Alta Lake State Park Alta Lake Area 1B OTTO ROAD [email protected] Eastern PATEROS WA 98846 Brian Hageman FORT WORDEN STATE PARK Anderson Lake (360) 344-4442 Olympic View Area 200 BATTERY WAY State Park [email protected] Southwest PORT TOWNSEND, WA 98368-3621 Chris Guidotti BATTLE GROUND STATE PARK Battle Ground Lake (360) 687-4621 Battle Ground Area PO BOX 148 State Park [email protected] Southwest HEISSON, WA 98622 Kevin Kratochvil RASAR STATE PARK (360) 757-0227 Bay View State Park Rasar Area 38730 CAPE HORN ROAD [email protected] Northwest CONCRETE, WA 98237 Chris Guidotti BATTLE GROUND STATE PARK Beacon Rock (509) 427-8265 Battle Ground Area PO BOX 148 State Park [email protected] Southwest HEISSON, WA 98622 Joel Pillers BELFAIR STATE PARK (360) 275-0668 Belfair State Park South Sound Area 3151 N.E. SR 300 [email protected] Southwest BELFAIR, WA 98528 Jack Hartt DECEPTION PASS STATE PARK Ben Ure Island Marine (360) 675-3767 Deception Pass Area 41020 STATE ROUTE 20 State Park [email protected] Northwest OAK HARBOR, WA 98277 Ted Morris BIRCH BAY STATE PARK (360) 371-2800 Birch Bay State Park Birch Bay Area 5105 HELWEG ROAD [email protected] Northwest BLAINE WA 98230 Dave Roe MANCHESTER STATE PARK Blake Island Marine (360) 731-8330 Blake -
Cadmium, Lead, Arsenic and Nickel in Wild Edible Mushrooms
THE FINNISH ENVIRONMENT 17 | 2006 ENVIRONMENTALYMPÄRISTÖN- Cadmium, lead, arsenic PROTECTIONSUOJELU and nickel in wild edible mushrooms Riina Pelkonen, Georg Alfthan and Olli Järvinen THE FINNISH ENVIRONMENT 17/2006 Cadmium, lead, arsenic and nickel in wild edible mushrooms Riina Pelkonen, Georg Alfthan and Olli Järvinen Helsinki 2006 Finnish Environment Institute THE FINNISH ENVIRONMENT 17 | 2006 Suomen ympäristökeskus Laboratorio Taitto: Callide/Terttu Halme Kansikuva(t): Riina Pelkonen Sisäsivujen kuvat: Figures 1 - 4: Copyright: Geologian tutkimuskeskus 1996 Figure 5: Suomen ympäristökeskus Julkaisu on saatavana myös internetistä: www.ymparisto.fi /julkaisut Edita Print Oy, Helsinki 2006 ISBN 952-11-2274-9 (nid.) ISBN 952-11-2275-7 (PDF) ISSN 1238-7312 (pain.) ISSN 1796-1637 (verkkoj.) PREFACE In Finland wild-growing products such as mushrooms and berries grow in abundance in forests and are traditionally used as a source of food by the Finns. Although the majority of edible mushrooms growing in Finnish forests are not consumed, picking mushrooms is a common activity for a large part of the population. Fungi are widely recognised to have a good nutritional value and in the recent years younger gener- ations in particular seem to have taken a culinary interest in mushrooms. As mushrooms may be freely picked and consumed there is no monitoring sys- tem to control the amounts of trace elements that enter the human body from the consumption of fungi. In Finland the levels of trace elements in fungi have not been extensively researched apart from the studies carried out in the turn of the 1970s and 1980s (Hinneri 1975, Laaksovirta & Alakuijala 1978, Laaksovirta & Lodenius 1979, Kuusi et al. -
Fungal Diversity in the Mediterranean Area
Fungal Diversity in the Mediterranean Area • Giuseppe Venturella Fungal Diversity in the Mediterranean Area Edited by Giuseppe Venturella Printed Edition of the Special Issue Published in Diversity www.mdpi.com/journal/diversity Fungal Diversity in the Mediterranean Area Fungal Diversity in the Mediterranean Area Editor Giuseppe Venturella MDPI • Basel • Beijing • Wuhan • Barcelona • Belgrade • Manchester • Tokyo • Cluj • Tianjin Editor Giuseppe Venturella University of Palermo Italy Editorial Office MDPI St. Alban-Anlage 66 4052 Basel, Switzerland This is a reprint of articles from the Special Issue published online in the open access journal Diversity (ISSN 1424-2818) (available at: https://www.mdpi.com/journal/diversity/special issues/ fungal diversity). For citation purposes, cite each article independently as indicated on the article page online and as indicated below: LastName, A.A.; LastName, B.B.; LastName, C.C. Article Title. Journal Name Year, Article Number, Page Range. ISBN 978-3-03936-978-2 (Hbk) ISBN 978-3-03936-979-9 (PDF) c 2020 by the authors. Articles in this book are Open Access and distributed under the Creative Commons Attribution (CC BY) license, which allows users to download, copy and build upon published articles, as long as the author and publisher are properly credited, which ensures maximum dissemination and a wider impact of our publications. The book as a whole is distributed by MDPI under the terms and conditions of the Creative Commons license CC BY-NC-ND. Contents About the Editor .............................................. vii Giuseppe Venturella Fungal Diversity in the Mediterranean Area Reprinted from: Diversity 2020, 12, 253, doi:10.3390/d12060253 .................... 1 Elias Polemis, Vassiliki Fryssouli, Vassileios Daskalopoulos and Georgios I. -
Native Plant List, Pdf Format
Appendix A: City of Bellingham Native Plant List December 2020 The City of Bellingham Native Plant List (Figure 1) includes plant species that are native to Bellingham watersheds (Figure 2). The native plant list applies to all habitat types, including riparian, upland, and wetland areas. The list was developed using specimen records from the Consortium of Pacific Northwest Herbaria and Bellingham plant checklists curated by Don Knoke, a volunteer at the University of Washington Herbarium. To improve plant establishment and protect the genetic resources of our local plant populations, the City recommends using native plants that were grown from seeds or cuttings collected from the Puget Trough Ecoregion (Figure 3). Obtaining native plants grown from material collected from the Puget Trough Ecoregion will help ensure the plants are adapted to the unique environmental conditions of Bellingham watersheds and are genetically similar to our local plant populations. A more thorough discussion of the rational and selection process is provided in the City of Bellingham Public Works Department Native Plant Materials Selection Guidelines, December 2020. Figure 1. City of Bellingham Native Plant List Ferns Common Name Scientific Name Family Bracken fern Pteridium aquilinum var. pubescens Dennstaedtiaceae Bristle-like quillwort Isoetes tenella Isoetaceae Common horsetail Equisetum arvense Equisetaceae Deer fern Struthiopteris spicant (Blechnum spicant) Blechnaceae Dream fern Aspidotis densa Pteridaceae Giant horsetail Equisetum telmateia ssp. braunii -
Boletus Edulis and Cistus Ladanifer: Characterization of Its Ectomycorrhizae, in Vitro Synthesis, and Realised Niche
UNIVERSIDAD DE MURCIA ESCUELA INTERNACIONAL DE DOCTORADO Boletus edulis and Cistus ladanifer: characterization of its ectomycorrhizae, in vitro synthesis, and realised niche. Boletus edulis y Cistus ladanifer: caracterización de sus ectomicorrizas, síntesis in vitro y área potencial. Dª. Beatriz Águeda Hernández 2014 UNIVERSIDAD DE MURCIA ESCUELA INTERNACIONAL DE DOCTORADO Boletus edulis AND Cistus ladanifer: CHARACTERIZATION OF ITS ECTOMYCORRHIZAE, in vitro SYNTHESIS, AND REALISED NICHE tesis doctoral BEATRIZ ÁGUEDA HERNÁNDEZ Memoria presentada para la obtención del grado de Doctor por la Universidad de Murcia: Dra. Luz Marina Fernández Toirán Directora, Universidad de Valladolid Dra. Asunción Morte Gómez Tutora, Universidad de Murcia 2014 Dª. Luz Marina Fernández Toirán, Profesora Contratada Doctora de la Universidad de Valladolid, como Directora, y Dª. Asunción Morte Gómez, Profesora Titular de la Universidad de Murcia, como Tutora, AUTORIZAN: La presentación de la Tesis Doctoral titulada: ‘Boletus edulis and Cistus ladanifer: characterization of its ectomycorrhizae, in vitro synthesis, and realised niche’, realizada por Dª Beatriz Águeda Hernández, bajo nuestra inmediata dirección y supervisión, y que presenta para la obtención del grado de Doctor por la Universidad de Murcia. En Murcia, a 31 de julio de 2014 Dra. Luz Marina Fernández Toirán Dra. Asunción Morte Gómez Área de Botánica. Departamento de Biología Vegetal Campus Universitario de Espinardo. 30100 Murcia T. 868 887 007 – www.um.es/web/biologia-vegetal Not everything that can be counted counts, and not everything that counts can be counted. Albert Einstein Le petit prince, alors, ne put contenir son admiration: -Que vous êtes belle! -N´est-ce pas, répondit doucement la fleur. Et je suis née meme temps que le soleil.. -
7/' / 7? Title: Composition, Distribution and Succession of Subal Ne Meadows In
AN ABSTRACT OF THE THESIS OF Jan Alan Henderson for theDoctor of Philosophy inPlant Ecology (Botany) presented on 9 7/' / 7? Title: Composition, Distribution and Succession of Subal ne Meadows in Mount Rainier National Park Abstract approved: --' Dr. W. W. Chilcote In 1970 a phytoscxiological reconnaissance consisting of 135 plots in the Subalpine Meadow Zone was made. These samples were sorted using an association table and several Alpine Zone and very early seral communities were set aside, An additional hundred plots taken by M. 3. Hamann were incorporated with these and compiled in another association table and com- bined in a two-dimensional ordination.This analysis yielded 18 major and 16 minor described community types which were clustered into five vegetation types. A key to the vegetation and community types is also presented. Soil moisture and temperature data were taken during 1971 and 1972 and are used to help characterize selected important communities. Soil moistures did not drop much during either season, although differences between corn- munities are apparent. The difference in temperatures (of the top 2 cm of soil) of the same selected communities were more striking. The Festuca domi- nated communities experienced soil temperatures over350C, while maximum temperatures in other communities rarely ranged over 20 C Low mght- time temperatures were relatively similar from conimumty to commumty, ranging from near freezing to about + 5° C. Several successional patterns were uncovered. In general the com- munities in the Low-Herbaceous Vegetation Type are early seral and are replaced by members of the Wet-Sedge, Lush-Herbaceous and the Dry-Grass Vegetation Types. -
<I>Neoalbatrellus Subcaeruleoporus</I>
ISSN (print) 0093-4666 © 2015. Mycotaxon, Ltd. ISSN (online) 2154-8889 MYCOTAXON http://dx.doi.org/10.5248/130.1191 Volume 130, pp. 1191–1202 October–December 2015 Neoalbatrellus subcaeruleoporus sp. nov. (Scutigeraceae) from western North America Serge Audet1* & Brian S. Luther2 11264, Gaillard, Québec, G3J 1J9, Canada 2 PSMS Office, Center for Urban Horticulture, University of Washington, Box 354115, Seattle, Washington 98195, U.S.A. * Corresponding author: [email protected] Abstract –Neoalbatrellus subcaeruleoporus is described as a new species. Its systematic position is supported by molecular and morphological analyses, and a key to the three Neoalbatrellus species is provided. A revised key to American and European species of Scutiger sensu lato (Albatrellopsis, Albatrellus, Laeticutis, Neoalbatrellus, Polypus, Polyporoletus, Polyporopsis, Scutiger s.s., Xanthoporus, and Xeroceps) is appended. Keywords –Albatrellaceae, caeruleoporus, correct family, genetic, Russulales Introduction The genus Neoalbatrellus was proposed by Audet (2010) and is distinguished from Albatrellus by the hymeniderm and the blue, black and brown colors of the basidiomata. Two species have been placed in Neoalbatrellus: N. caeruleoporus and N. yasudae (Audet 2010). Their trophic status is poorly understood and specific ectomycorrhizal host trees have not been confirmed, although N. caeruleoporus is often found underTsuga (Gilbertson & Ryvarden 1986). The presence of extracellular laccase has been reported in basidiomata of N. caeruleoporus (Marr et al. 1986). The closest genus to Neoalbatrellus is Albatrellopsis, based on molecular (ITS) and the dimeric meroterpenoid pigment, grifolinone B (Zhou & Liu 2010). The correct family for these genera is Scutigeraceae Bondartsev & Singer ex Singer 1969, a name that has priority over Albatrellaceae Nuss 1980 (Audet 2010: 439).