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The Mycological Society of San Francisco • Jan. 2016, Vol. 67:05
The Mycological Society of San Francisco • Jan. 2016, vol. 67:05 Table of Contents JANUARY 19 General Meeting Speaker Mushroom of the Month by K. Litchfield 1 President Post by B. Wenck-Reilly 2 Robert Dale Rogers Schizophyllum by D. Arora & W. So 4 Culinary Corner by H. Lunan 5 Hospitality by E. Multhaup 5 Holiday Dinner 2015 Report by E. Multhaup 6 Bizarre World of Fungi: 1965 by B. Sommer 7 Academic Quadrant by J. Shay 8 Announcements / Events 9 2015 Fungus Fair by J. Shay 10 David Arora’s talk by D. Tighe 11 Cultivation Quarters by K. Litchfield 12 Fungus Fair Species list by D. Nolan 13 Calendar 15 Mushroom of the Month: Chanterelle by Ken Litchfield Twenty-One Myths of Medicinal Mushrooms: Information on the use of medicinal mushrooms for This month’s profiled mushroom is the delectable Chan- preventive and therapeutic modalities has increased terelle, one of the most distinctive and easily recognized mush- on the internet in the past decade. Some is based on rooms in all its many colors and meaty forms. These golden, yellow, science and most on marketing. This talk will look white, rosy, scarlet, purple, blue, and black cornucopias of succu- at 21 common misconceptions, helping separate fact lent brawn belong to the genera Cantharellus, Craterellus, Gomphus, from fiction. Turbinellus, and Polyozellus. Rather than popping up quickly from quiescent primordial buttons that only need enough rain to expand About the speaker: the preformed babies, Robert Dale Rogers has been an herbalist for over forty these mushrooms re- years. He has a Bachelor of Science from the Univer- quire an extended period sity of Alberta, where he is an assistant clinical profes- of slower growth and sor in Family Medicine. -
<I>Craterellus Excelsus</I>
MYCOTAXON Volume 107, pp. 201–208 January–March 2009 Craterellus excelsus sp. nov. from Guyana Terry W. Henkel1*, M. Catherine Aime2 & Heather K. Mehl1 1Department of Biological Sciences, Humboldt State University Arcata, CA 95521, USA. 2Department of Plant Pathology and Crop Physiology Louisiana State University Agricultural Center Baton Rouge, LA 70803, USA Abstract — Craterellus excelsus (Cantharellaceae, Cantharellales, Basidiomycota) is described from the Pakaraima Mountains of Guyana, where it occurs in rain forests dominated by ectomycorrhizal Dicymbe spp. (Caesalpiniaceae). Craterellus excelsus is noteworthy for its tall (up to 150 mm), persistent, abundant basidiomata that develop in large caespitose clusters. Macromorphological, micromorphological, and habitat data are provided for the new species. Keywords — monodominant forest, tropical fungi, taxonomy, Guiana Shield Introduction In the primary rain forests of Guyana’s Pakaraima Mountains, species of Craterellus and Cantharellus (Cantharellaceae, Cantharellales, Basidiomycota) are conspicuous components of the macromycota associated with ectomycorrhizal (EM) canopy trees of the genus Dicymbe (Caesalpiniaceae, tribe Amherstieae) (Henkel et al. 2002, 2004). Taxa from the Cantharellales occurring in these forests include Cantharellus guyanensis, C. atratus, C. pleurotoides, three undescribed species of Craterellus, and >15 Clavulina species, a number of which remain undescribed (Thacker & Henkel 2004, Henkel et al. 2005, 2006). Here we describe Craterellus excelsus as a distinct new species based on its grey- brown, persistent basidiomata that are regularly >100 mm tall and occur in large caespitose clusters, and its long basidia of variable lengths (75−101 μm) with varying numbers of sterigmata (2−6). Materials and methods Collections were made during the May–July rainy seasons of 2000–2004 from the Upper Potaro River Basin, within a 5 km radius of a permanent base camp *Corresponding author E-mail: [email protected] 202 .. -
Systematics of Division Basidiomycota 2
References: Kirk PM, Cannon PF, Minter DW, Stalpers JA. 2008. Dictionary of the Fungi (10th ed.).Wallingford, UK: CABI. Webster, J., & Weber, R. (2007). Introduction to fungi. Cambridge, UK: Cambridge University Press. SYSTEMATICS OF DIVISION BASIDIOMYCOTA 2 THELEPHOROID CLADE This includes the order Thelephorales, a small group of predominantly ectomycorrhizal fungi with variable basidiocarps. The most important genus is Thelephora. T. terrestris produces clusters of fanshaped basidiocarps which are chocolate-brown in colour with a paler margin. They are often formed around the stem of young trees, seemingly ‘choking’ them. Basidiocarps of T. terrestris superficially resemble those of Stereum but are monomitic, composed of clamped generative hyphae only. The basidiospores are brown and warty. Thelephora terrestris fruits in association with coniferous trees growing on light sandy soils and heaths. It isone of a group of early-stage ectomycorrhizal associates of a variety of trees and also forms mycorrhiza with Arbutus menziesii, a member of the Ericaceae (Webster& Weber, 2007). HYMENOCHAETOID CLADE One feature that distinguishes the five Homobasidiomycete clades considered in the previous sections from the remaining three clades is the structure of the parenthesome, i.e. the membranous structure overarching the septal pore. In the five clades already described, the typical homobasidiomycete dolipore with a perforated parenthesome is found, whereas in the hymenochaetoid, cantharelloid and gomphoid_phalloid clades shown in, the parenthesome is generally imperforate. Imperforate parenthesomes are also found in certain Heterobasidiomycetes, namely Dacrymycetales and Auriculariales. The hymenochaetoid clade comprises about 630 species recruited from three families, namely the entire Hymenochaetaceae and parts of Corticiaceae and Polyporaceae (Webster& Weber, 2007). -
Pipestem Foray Overview
Volume 49:1 January ⁄ February 2008 www.namyco.org Pipestem Foray Overview An East-Coaster’s Perspective A West-Coaster’s Perspective by Dave Wasilewski by Debbie Viess For about 25 years now I have As Steve Trudell rightly pointed out hunted and studied wild mush- to me, don’t gloat about your mush- rooms, but I’ve never been active in rooms until they are safely in your a club. The NAMA Orson K. Miller basket! The continuing “Curse of Memorial Foray held in Pipestem, NAMA” (some call it global warm- WV, this past August was the first ing) slipped in the back door, behind such event that I have ever at- the earlier and heartening West tended. Virginia thunderstorms. Extreme I must admit that, as I drove heat and lack of rain for the previ- south on Interstate 81 through two ous couple of weeks made condi- solid hours of Pennsylvania rainfall tions on the ground challenging for on an eight-hour trip to a place hopeful finders of fungi. Chlorosplenium aeruginascens, one of where little or no rain had fallen for Luckily, my Southern Belle the many delights found at Pipestem. over a week, for the purpose of hostess with the mostest, Coleman hunting wild mushrooms, I felt a bit McCleneghan, took me on a few names like Gyroporus and Pulvero- conflicted. My mind wandered pre-NAMA forays in Virginia, where boletus, tucked among the through conifer groves in the conditions were much improved. My many shades of forest green and Poconos where imaginary boletes very first walk ever along the brown. -
9B Taxonomy to Genus
Fungus and Lichen Genera in the NEMF Database Taxonomic hierarchy: phyllum > class (-etes) > order (-ales) > family (-ceae) > genus. Total number of genera in the database: 526 Anamorphic fungi (see p. 4), which are disseminated by propagules not formed from cells where meiosis has occurred, are presently not grouped by class, order, etc. Most propagules can be referred to as "conidia," but some are derived from unspecialized vegetative mycelium. A significant number are correlated with fungal states that produce spores derived from cells where meiosis has, or is assumed to have, occurred. These are, where known, members of the ascomycetes or basidiomycetes. However, in many cases, they are still undescribed, unrecognized or poorly known. (Explanation paraphrased from "Dictionary of the Fungi, 9th Edition.") Principal authority for this taxonomy is the Dictionary of the Fungi and its online database, www.indexfungorum.org. For lichens, see Lecanoromycetes on p. 3. Basidiomycota Aegerita Poria Macrolepiota Grandinia Poronidulus Melanophyllum Agaricomycetes Hyphoderma Postia Amanitaceae Cantharellales Meripilaceae Pycnoporellus Amanita Cantharellaceae Abortiporus Skeletocutis Bolbitiaceae Cantharellus Antrodia Trichaptum Agrocybe Craterellus Grifola Tyromyces Bolbitius Clavulinaceae Meripilus Sistotremataceae Conocybe Clavulina Physisporinus Trechispora Hebeloma Hydnaceae Meruliaceae Sparassidaceae Panaeolina Hydnum Climacodon Sparassis Clavariaceae Polyporales Gloeoporus Steccherinaceae Clavaria Albatrellaceae Hyphodermopsis Antrodiella -
The Effect of Decayed Or Downed Wood on the Structure and Function of Ectomycorrhizal Fungal Communities at a High Elevation Forest
The effect of decayed or downed wood on the structure and function of ectomycorrhizal fungal communities at a high elevation forest by Jennifer Karen Marie Walker B.Sc., The University of Northern British Columbia, 2003 M.Sc., The University of Northern British Columbia, 2006 A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY in The College of Graduate Studies (Biology) THE UNIVERSITY OF BRITISH COLUMBIA (Okanagan) March 2012 !Jennifer Karen Marie Walker, 2012 Abstract Shifts in ectomycorrhizal (ECM) fungal community composition occur after clearcut logging, resulting in the loss of forest-associated fungi and potential ecosystem function. Coarse woody debris (CWD) includes downed wood generated during logging; decayed downed wood is a remnant of the original forest, and important habitat for ECM fungi. Over the medium term, while logs remain hard, it is not known if they influence ECM fungal habitat. I tested for effects of downed wood on ECM fungal communities by examining ECM roots and fungal hyphae of 10-yr-old saplings in CWD retention and removal plots in a subalpine ecosystem. I then tested whether downed and decayed wood provided ECM fungal habitat by planting nonmycorrhizal spruce seedlings in decayed wood, downed wood, and mineral soil microsites in the clearcuts and adjacent forest plots, and harvested them 1 and 2 years later. I tested for differences in the community structure of ECM root tips (Sanger sequencing) among all plots and microsites, and of ECM fungal hyphae (pyrosequencing) in forest microsites. I assayed the activities of eight extracellular enzymes in order to compare community function related to nutrient acquisition. -
Biology of Marine Fungi 20130420 151718.Pdf
Progress in Molecular and Subcellular Biology Series Editors Werner E.G. Mu¨ller Philippe Jeanteur, Robert E. Rhoads, Ðurðica Ugarkovic´, Ma´rcio Reis Custo´dio 53 Volumes Published in the Series Progress in Molecular Subseries: and Subcellular Biology Marine Molecular Biotechnology Volume 36 Volume 37 Viruses and Apoptosis Sponges (Porifera) C. Alonso (Ed.) W.E.G. Mu¨ller (Ed.) Volume 38 Volume 39 Epigenetics and Chromatin Echinodermata Ph. Jeanteur (Ed.) V. Matranga (Ed.) Volume 40 Volume 42 Developmental Biology of Neoplastic Antifouling Compounds Growth N. Fusetani and A.S. Clare (Eds.) A. Macieira-Coelho (Ed.) Volume 43 Volume 41 Molluscs Molecular Basis of Symbiosis G. Cimino and M. Gavagnin (Eds.) J. Overmann (Ed.) Volume 46 Volume 44 Marine Toxins as Research Tools Alternative Splicing and Disease N. Fusetani and W. Kem (Eds.) Ph. Jeanlevr (Ed.) Volume 47 Volume 45 Biosilica in Evolution, Morphogenesis, Asymmetric Cell Division and Nanobiotechnology A. Macieira Coelho (Ed.) W.E.G. Mu¨ller and M.A. Grachev (Eds.) Volume 48 Volume 52 Centromere Molecular Biomineralization Ðurdica- Ugarkovic´ (Ed.) W.E.G. Mu¨ller (Ed.) Volume 49 Volume 53 Aestivation Biology of Marine Fungi C.A. Navas and J.E. Carvalho (Eds.) C. Raghukumar (Ed.) Volume 50 miRNA Regulation of the Translational Machinery R.E. Rhoads (Ed.) Volume 51 Long Non-Coding RNAs Ðurdica- Ugarkovic (Ed.) Chandralata Raghukumar Editor Biology of Marine Fungi Editor Dr. Chandralata Raghukumar National Institute of Oceanography Marine Biotechnology Laboratory Dona Paula 403004 Panjim India [email protected] ISSN 0079-6484 ISBN 978-3-642-23341-8 e-ISBN 978-3-642-23342-5 DOI 10.1007/978-3-642-23342-5 Springer Heidelberg Dordrecht London New York Library of Congress Control Number: 2011943185 # Springer-Verlag Berlin Heidelberg 2012 This work is subject to copyright. -
Polyozellus Multiplex-An Example of Our Mycological Ignorance. Osprey 37:20-22
20 21 Polyozellus Multiplex - An Example of Our Mycological Ignorance by Andrus Voitk Polyozellus multiplex, the blue (or black) chanterelle, shown in Figure 1, grows as a large cluster of black or very dark bluish-purple fan- shaped leaves, arising out of a wide, common stalk. The sporulating surface, on the outside of each fan, is made up of folds, somewhat resembling thick, forked, decurrent gills. The spore print is white, giving mature specimens a dull bluish-gray appearance on the outside, Figure 1 - Polyozellus multiplex, Stanleyville Trail, contrasting with the shinier blackish purple on Gros Morne National Park, September, 2000. the inside of each leaf. The same trees are still there but this gorgeous ectomycorrhizal mushroom has not been seen in that Classical morphological taxonomy considered location since. I am now aware of three places where Polyozellus to be a relative of the chantarelle with this mushroom has been found to fruit. In 1-5 follow- its fold-like gills, along with the genus Gomphus, up years it has not been found to fruit in any of these whose sporulating surface is virtually identical to places again. that of P. multiplex. Recent DNA studies have left Gomphus as a distant relative of the chanterelle but placed P. multiplex with earth fans, Class Telephorales, Family Telephuraceae. It doesn’t seem to fit readily with either and no doubt the future has more family unrest in store for poor P. multiplex. Among interesting properties of this good edible* is its ability to slow certain cell replication. Animal experiments suggest P. multiplex may, among other things, prevent stomach cancer (1). -
Craterellus Tubaeformis (Fries) Quélet ROD Name Cantharellus Tubaeformis Family Cantharellaceae Morphological Habit Chanterelle
S3 - 58 Craterellus tubaeformis (Fries) Quélet ROD name Cantharellus tubaeformis Family Cantharellaceae Morphological Habit chanterelle Description: CAP 1-3 (5) cm broad, convex to plane or broadly depressed, with an arched incurved margin at first, margin finally spreading or uplifted and becoming crenate to variously lobed, occasionally somewhat funnel shaped in age, usually not perforated in the disc at first but frequently becoming so in age, surface moist and more or less uneven, dark sordid yellow-brown. CONTEXT membranous, fragile, yellow-brown to gray-brown. ODOR AND TASTE not distinctive. GILLS decurrent, narrow and foldlike, dichotomously forked, yellow-gray to gray-brown. STEM 30-60 mm long, 3-7 mm thick, stuffed but becoming hollow and flabby, subequal, often compressed or furrowed, glabrous, dark to pale gray-brown above, usually off-white at base. PILEIPELLIS of hyaline, interwoven hyphae 6-12 µm in diam., the hyphae on the surface yellow-brown but otherwise not differentiated from the context. BASIDIA 64-82 x 9-11 µm, clavate, hyaline, flexuous toward the base, 2-4 spored. CYSTIDIA absent. CLAMP CONNECTIONS abundant. SPORES ellipsoid to ovoid, (8) 9-11 x 5.5-7 µm, smooth, hyaline, inamyloid, spore print white to creamy white. Distinguishing Features: The chanterellelike sporocarp with hollow stipe separates Craterellus tubaeformis from all other mushrooms. Distribution: Common and widely distributed in northwestern North America including northern Idaho; also eastern North America, including Appalachian Mountains and Canadian maritime provinces; also across northern Europe. Known from many dozens of locations throughout the range of the Northwest Forest Plan. Substrate and Habitat: On wet soil, often along streams or near springs or in bogs under conifers; also juxtaposed to rotten logs. -
Il/Ill Signature Redactsignature Redacted for Privacy
AN ABSTRACT OF THE THESIS OF Matthew James Trappe for the degree of Master of Science in Forest Science presented on September 13, 2001. Title: Ecology of Craterellus tubaeformj',AI in Westerrj..Qron.il/Ill Signature redactSignature redacted for privacy. Abstract approved: A. Castellano Robert P. Griffith Craterellus tuba eformis is a small to medium-sized forest mushroom that is fairly common in the Douglas-fir/western hemlock forests of the Pacific Northwestern United States and is most often associated with decayed coarse woody debris. In this study, the mycorrhizae of Craterellus tubaeformis in western Oregon is identified by DNA analysis using polymerase chain reaction (PCR) amplification and restriction fragment length polymorphism (RFLP) typing, and the mantle morphology isdescribed. Host associations with western hemlock, Douglas-fir5 and Sitka spruce are identified using the same molecular techniques, with Craterellus tubaeformis most commonly associated with western hemlock. Differences in genetic sequences and host associations between western North America, eastern North America, and. Europe are presented, and the possibility that variants of Craterellus. tubaeformis from the different geographies might deserve their own species epithets is discussed. The dependency of Craterellus tubaeformis on late seral stands and abundance of coarse woody debris was quantified by surveying 64 plots in the Coast and Cascade ranges of western Oregon.Logistic regression showed that the odds of Craterellus tubaeformis occurrence increased with stand age and coarse woody debris (CWD) volumes, however it is often found in younger stands. The likelihood of Craterellus tubaeformis occurrence in a stand was highly correlated to the presence of western hemlock. Linear regression analysis showed no significant relationships between stand age, CWD volume, slope, elevation, or aspect on Craterellus tuba eformis biomass productivity, though well- decayed CWD was the substrate for 88% of the collected biomass. -
How to Distinguish Amanita Smithiana from Matsutake and Catathelasma Species
VOLUME 57: 1 JANUARY-FEBRUARY 2017 www.namyco.org How to Distinguish Amanita smithiana from Matsutake and Catathelasma species By Michael W. Beug: Chair, NAMA Toxicology Committee A recent rash of mushroom poisonings involving liver failure in Oregon prompted Michael Beug to issue the following photos and information on distinguishing the differences between the toxic Amanita smithiana and edible Matsutake and Catathelasma. Distinguishing the choice edible Amanita smithiana Amanita smithiana Matsutake (Tricholoma magnivelare) from the highly poisonous Amanita smithiana is best done by laying the stipe (stem) of the mushroom in the palm of your hand and then squeezing down on the stipe with your thumb, applying as much pressure as you can. Amanita smithiana is very firm but if you squeeze hard, the stipe will shatter. Matsutake The stipe of the Matsutake is much denser and will not shatter (unless it is riddled with insect larvae and is no longer in good edible condition). There are other important differences. The flesh of Matsutake peels or shreds like string cheese. Also, the stipe of the Matsutake is widest near the gills Matsutake and tapers gradually to a point while the stipe of Amanita smithiana tends to be bulbous and is usually widest right at ground level. The partial veil and ring of a Matsutake is membranous while the partial veil and ring of Amanita smithiana is powdery and readily flocculates into small pieces (often disappearing entirely). For most people the difference in odor is very distinctive. Most collections of Amanita smithiana have a bleach-like odor while Matsutake has a distinctive smell of old gym socks and cinnamon redhots (however, not all people can distinguish the odors). -
Notes, Outline and Divergence Times of Basidiomycota
Fungal Diversity (2019) 99:105–367 https://doi.org/10.1007/s13225-019-00435-4 (0123456789().,-volV)(0123456789().,- volV) Notes, outline and divergence times of Basidiomycota 1,2,3 1,4 3 5 5 Mao-Qiang He • Rui-Lin Zhao • Kevin D. Hyde • Dominik Begerow • Martin Kemler • 6 7 8,9 10 11 Andrey Yurkov • Eric H. C. McKenzie • Olivier Raspe´ • Makoto Kakishima • Santiago Sa´nchez-Ramı´rez • 12 13 14 15 16 Else C. Vellinga • Roy Halling • Viktor Papp • Ivan V. Zmitrovich • Bart Buyck • 8,9 3 17 18 1 Damien Ertz • Nalin N. Wijayawardene • Bao-Kai Cui • Nathan Schoutteten • Xin-Zhan Liu • 19 1 1,3 1 1 1 Tai-Hui Li • Yi-Jian Yao • Xin-Yu Zhu • An-Qi Liu • Guo-Jie Li • Ming-Zhe Zhang • 1 1 20 21,22 23 Zhi-Lin Ling • Bin Cao • Vladimı´r Antonı´n • Teun Boekhout • Bianca Denise Barbosa da Silva • 18 24 25 26 27 Eske De Crop • Cony Decock • Ba´lint Dima • Arun Kumar Dutta • Jack W. Fell • 28 29 30 31 Jo´ zsef Geml • Masoomeh Ghobad-Nejhad • Admir J. Giachini • Tatiana B. Gibertoni • 32 33,34 17 35 Sergio P. Gorjo´ n • Danny Haelewaters • Shuang-Hui He • Brendan P. Hodkinson • 36 37 38 39 40,41 Egon Horak • Tamotsu Hoshino • Alfredo Justo • Young Woon Lim • Nelson Menolli Jr. • 42 43,44 45 46 47 Armin Mesˇic´ • Jean-Marc Moncalvo • Gregory M. Mueller • La´szlo´ G. Nagy • R. Henrik Nilsson • 48 48 49 2 Machiel Noordeloos • Jorinde Nuytinck • Takamichi Orihara • Cheewangkoon Ratchadawan • 50,51 52 53 Mario Rajchenberg • Alexandre G.