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Mycelial Compatibility in Amylostereum Areolatum
Mycelial compatibility in Amylostereum areolatum Magrieta Aletta van der Nest © University of Pretoria © University of Pretoria Mycelial compatibility in Amylostereum areolatum by Magrieta Aletta van der Nest Promotor: Prof. B.D. Wingfield Co-promotor: Prof. M.J. Wingfield Prof. B. Slippers Prof. J. Stenlid Submitted in partial fulfilment of the requirements for the degree of Philosophiae Doctor in the Faculty of Natural and Agricultural Sciences, Department of Genetics at the University of Pretoria. September 2010 © University of Pretoria DECLARATION I, Magrieta Aletta van der Nest, declare that this thesis, which I hereby submit for the degree Philosophiae Doctor at the University of Pretoria, is my own work and has not been submitted by me at this or any other tertiary institution. SIGNATURE: DATE: © University of Pretoria TABLE OF CONTENTS ACKNOWLEDGEMENTS ................................................................................................... i PREFACE ............................................................................................................................... ii CHAPTER 1 ........................................................................................................................... 1 LITERATURE REVIEW: The molecular basis of vegetative incompatibility in fungi, with specific reference to Basidiomycetes CHAPTER 2 ......................................................................................................................... 44 Genetics of Amylostereum species associated with Siricidae -
<I>Sarcoporia Polyspora</I>
ISSN (print) 0093-4666 © 2015. Mycotaxon, Ltd. ISSN (online) 2154-8889 MYCOTAXON http://dx.doi.org/10.5248/130.279 Volume 130, pp. 279–287 January–March 2015 Geographic distribution of Sarcoporia polyspora and S. longitubulata sp. nov. Josef Vlasák1*, Josef Vlasák Jr., Juha Kinnunen2, & Viacheslav Spirin2 1Biol. Centre of the Academy of Sciences of the Czech Republic, Branišovská 31, CZ-370 05 České Budějovice, Czech Rep. 2Botanical Museum, P.O. Box 7, FI-00014 University of Helsinki, Finland * Correspondence to: [email protected] Abstract — DNA study of Sarcoporia polyspora (= Parmastomyces transmutans) revealed only negligible sequence differences between conifer-dwelling specimens with cartilaginous layer in the context from USA, Brazil, Europe, and Far East Asia, but a very different sequence from three resupinate and hardwood-bound collections without such a layer and with slightly narrower and pale brown spores from USA and Madeira Islands. This fungus, found also among historical USA collections of S. polyspora in the BPI herbarium, is described here as Sarcoporia longitubulata. The phylogenetic position ofSarcoporia is discussed. Key words — Basidiomycota, brown rot fungi, molecular taxonomy, Parmastomyces kravtzevianus Introduction Sarcoporia polyspora P. Karst. is a very distinct, brown-rot polypore with soft, resupinate to effused-reflexed basidiomes that are white to crème at first but turn reddish-brown after bruising or drying. It can be easily recognized by its ellipsoid and thick-walled, dextrinoid spores, which are quite unique in polypores. The species is rare in Europe but rather common in North America (on Tsuga spp. and Pinus spp.) and in Asia (Vlasák & Kout 2010, Dai 2012). -
Checklist of Lichenicolous Fungi and Lichenicolous Lichens of Svalbard, Including New Species, New Records and Revisions
Herzogia 26 (2), 2013: 323 –359 323 Checklist of lichenicolous fungi and lichenicolous lichens of Svalbard, including new species, new records and revisions Mikhail P. Zhurbenko* & Wolfgang von Brackel Abstract: Zhurbenko, M. P. & Brackel, W. v. 2013. Checklist of lichenicolous fungi and lichenicolous lichens of Svalbard, including new species, new records and revisions. – Herzogia 26: 323 –359. Hainesia bryonorae Zhurb. (on Bryonora castanea), Lichenochora caloplacae Zhurb. (on Caloplaca species), Sphaerellothecium epilecanora Zhurb. (on Lecanora epibryon), and Trimmatostroma cetrariae Brackel (on Cetraria is- landica) are described as new to science. Forty four species of lichenicolous fungi (Arthonia apotheciorum, A. aspicili- ae, A. epiphyscia, A. molendoi, A. pannariae, A. peltigerina, Cercidospora ochrolechiae, C. trypetheliza, C. verrucosar- ia, Dacampia engeliana, Dactylospora aeruginosa, D. frigida, Endococcus fusiger, E. sendtneri, Epibryon conductrix, Epilichen glauconigellus, Lichenochora coppinsii, L. weillii, Lichenopeltella peltigericola, L. santessonii, Lichenostigma chlaroterae, L. maureri, Llimoniella vinosa, Merismatium decolorans, M. heterophractum, Muellerella atricola, M. erratica, Pronectria erythrinella, Protothelenella croceae, Skyttella mulleri, Sphaerellothecium parmeliae, Sphaeropezia santessonii, S. thamnoliae, Stigmidium cladoniicola, S. collematis, S. frigidum, S. leucophlebiae, S. mycobilimbiae, S. pseudopeltideae, Taeniolella pertusariicola, Tremella cetrariicola, Xenonectriella lutescens, X. ornamentata, -
Research Journal of Pharmaceutical, Biological and Chemical Sciences
ISSN: 0975-8585 Research Journal of Pharmaceutical, Biological and Chemical Sciences Popularity of species of polypores which are parasitic upon oaks in coppice oakeries of the South-Western Central Russian Upland in Russian Federation. Alexander Vladimirovich Dunayev*, Valeriy Konstantinovich Tokhtar, Elena Nikolaevna Dunayeva, and Svetlana Viсtorovna Kalugina. Belgorod State National Research University, Pobedy St., 85, Belgorod, 308015, Russia. ABSTRACT The article deals with research of popularity of polypores species (Polyporaceae sensu lato), which are parasitic upon living English oaks Quercus robur L. in coppice oakeries of the South-Western Central Russian Upland in the context of their eco-biological peculiarities. It was demonstrated that the most popular species are those for which an oak is a principal host, not an accidental one. These species also have effective parasitic properties and are able to spread in forest stands, from tree to tree. Keywords: polypores, Quercus robur L., coppice forest stand, obligate parasite, facultative saprotroph, facultative parasite, popularity. *Corresponding author September - October 2014 RJPBCS 5(5) Page No. 1691 ISSN: 0975-8585 INTRODUCTION Polypores Polyporaceae s. l. is a group of basidium fungi which is traditionnaly discriminated on the basis of formal resemblance, including species of wood destroyers, having sessile (or rarer extended) fruit bodies and tube (or labyrinth-like or gill-bearing) hymenophore. Many of them are parasites housing on living trees of forest-making species, or pathogens – agents of root, butt or trunk rot. Rot’s development can lead to attenuation, drying, wind breakage or windfall of stressed trees. On living trees Quercus robur L., which is the main forest-making species of autochthonous forest steppe oakeries in Eastern Europe, in conditions of Central Russian Upland, we can find nearly 10 species of polypores [1-3], belonging to orders Agaricales, Hymenochaetales, Polyporales (class Agaricomicetes, division Basidiomycota [4]). -
Reviewing the World's Edible Mushroom Species: a New
Received: 5 September 2020 Revised: 4 December 2020 Accepted: 21 December 2020 DOI: 10.1111/1541-4337.12708 COMPREHENSIVE REVIEWS IN FOOD SCIENCE AND FOOD SAFETY Reviewing the world’s edible mushroom species: A new evidence-based classification system Huili Li1,2,3 Yang Tian4 Nelson Menolli Jr5,6 Lei Ye1,2,3 Samantha C. Karunarathna1,2,3 Jesus Perez-Moreno7 Mohammad Mahmudur Rahman8 Md Harunur Rashid8 Pheng Phengsintham9 Leela Rizal10 Taiga Kasuya11 Young Woon Lim12 Arun Kumar Dutta13 Abdul Nasir Khalid14 Le Thanh Huyen15 Marilen Parungao Balolong16 Gautam Baruah17 Sumedha Madawala18 Naritsada Thongklang19,20 Kevin D. Hyde19,20,21 Paul M. Kirk22 Jianchu Xu1,2,3 Jun Sheng23 Eric Boa24 Peter E. Mortimer1,3 1 CAS Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan, China 2 East and Central Asia Regional Office, World Agroforestry Centre (ICRAF), Kunming, Yunnan, China 3 Centre for Mountain Futures, Kunming Institute of Botany, Kunming, Yunnan, China 4 College of Food Science and Technology, Yunnan Agricultural University, Kunming, Yunnan, China 5 Núcleo de Pesquisa em Micologia, Instituto de Botânica, São Paulo, Brazil 6 Departamento de Ciências da Natureza e Matemática (DCM), Subárea de Biologia (SAB), Instituto Federal de Educação, Ciência e Tecnologia de São Paulo (IFSP), São Paulo, Brazil 7 Colegio de Postgraduados, Campus Montecillo, Texcoco, México 8 Global Centre for Environmental Remediation (GCER), Faculty of Science, The University of Newcastle, -
A Phylogenetic Overview of the Antrodia Clade (Basidiomycota, Polyporales)
Mycologia, 105(6), 2013, pp. 1391–1411. DOI: 10.3852/13-051 # 2013 by The Mycological Society of America, Lawrence, KS 66044-8897 A phylogenetic overview of the antrodia clade (Basidiomycota, Polyporales) Beatriz Ortiz-Santana1 phylogenetic studies also have recognized the genera Daniel L. Lindner Amylocystis, Dacryobolus, Melanoporia, Pycnoporellus, US Forest Service, Northern Research Station, Center for Sarcoporia and Wolfiporia as part of the antrodia clade Forest Mycology Research, One Gifford Pinchot Drive, (SY Kim and Jung 2000, 2001; Binder and Hibbett Madison, Wisconsin 53726 2002; Hibbett and Binder 2002; SY Kim et al. 2003; Otto Miettinen Binder et al. 2005), while the genera Antrodia, Botanical Museum, University of Helsinki, PO Box 7, Daedalea, Fomitopsis, Laetiporus and Sparassis have 00014, Helsinki, Finland received attention in regard to species delimitation (SY Kim et al. 2001, 2003; KM Kim et al. 2005, 2007; Alfredo Justo Desjardin et al. 2004; Wang et al. 2004; Wu et al. 2004; David S. Hibbett Dai et al. 2006; Blanco-Dios et al. 2006; Chiu 2007; Clark University, Biology Department, 950 Main Street, Worcester, Massachusetts 01610 Lindner and Banik 2008; Yu et al. 2010; Banik et al. 2010, 2012; Garcia-Sandoval et al. 2011; Lindner et al. 2011; Rajchenberg et al. 2011; Zhou and Wei 2012; Abstract: Phylogenetic relationships among mem- Bernicchia et al. 2012; Spirin et al. 2012, 2013). These bers of the antrodia clade were investigated with studies also established that some of the genera are molecular data from two nuclear ribosomal DNA not monophyletic and several modifications have regions, LSU and ITS. A total of 123 species been proposed: the segregation of Antrodia s.l. -
Pertusaria Georgeana Var. Goonooensis Is Described As New to Science
The striking rust-red colour of the surface of Porpidia macrocarpa is thought to result from a high “luxury” accumulation of iron. The species is known from New Zealand and Australia in the Southern Hemisphere and from North America, Europe, and Asia in the Northern Hemisphere. 1 mm CONTENTS ADDITIONAL LICHEN RECORDS FROM NEW ZEALAND Fryday, AM (47) Coccotrema corallinum Messuti and C. pocillarium (C.E.Cumm.) Brodo .... 3 ADDITIONAL LICHEN RECORDS FROM AUSTRALIA Archer, AW (63) Graphis cleistoblephara Nyl. and G. plagiocarpa Fée ........................... 6 Elix, JA (64) ......................................................................................................................... 8 RECENT LITERATURE ON AUSTRALASIAN LICHENS ......................................... 16 ANNOUNCEMENT AND NEWS 18th meeting of Australasian lichenologists 2008 ...................................................... 17 Ray Cranfield awarded Churchill Fellowship ............................................................ 17 ARTICLES Archer, AW; Elix, JA—Two new species in the Australian Graphidaceae (lichenized Ascomycota) ................................................................................................................... 18 Elix, JA—Further new crustose lichens (Ascomycota) from Australia ................... 21 Elix, JA; Archer, AW—A new variety of Pertusaria georgeana (lichenized Ascomy- cota) containing a new depside .................................................................................. 26 Elix, JA—A new species of Xanthoparmelia -
<I>Lichenostigma Epirupestre</I> a New Lichenicolous Species On
MYCOTAXON Volume 107, pp. 189–195 January–March 2009 Lichenostigma epirupestre, a new lichenicolous species on Pertusaria from Spain Sergio Pérez-Ortega1 & Vicent Calatayud2 [email protected] Departamento de Biología Vegetal II, Facultad de Farmacia Universidad Complutense de Madrid Plaza Ramón y Cajal, Ciudad Universitaria, ES-28040 Madrid, SPAIN 2Fundación CEAM C/ Charles R. Darwin 14, Parc Tecnològic, E–46980 Paterna, València, Spain Abstract—The new species Lichenostigma epirupestre is described from three localities in Central Spain, growing on Pertusaria pertusa var. rupestris. Remarks on its taxonomy and closely related species are made and a key to the species of Lichenostigma subgenus Lichenostigma is also included. Key words—Iberian Peninsula, lichenicolous fungi, lichens Introduction The genus Lichenostigma was introduced for L. maureri Hafellner (Hafellner 1982) and, since then, a total of 21 species (after www.indexfungorum.org) have been referred to it. Two subgenera are recognized: Lichenostigma and Lichenogramma (Navarro-Rosinés & Hafellner 1996, Calatayud et al. 2002). Species belonging to subgenus Lichenostigma are characterized by having cushion-like ascomata and by the absence of visible vegetative hyphae or strands connecting several ascomata on the surface of the thallus. Taxa included in subgenus Lichenogramma show rounded or elongate ascomata that are interconnected by brown hyphae or pluricellular strands. While most species can easily be referred to one of these two subgenera, a few species show some intermediate features. This is the case of species in which the rounded shape of the ascomata is typical of subgenus Lichenostigma, but developing immersed (not visible on the host thallus) brown vegetative hyphae, or others that only occasionally develop superficial hyphal strands but only occasionally (Calatayud & Barreno 2003, Halıcı & Hawksworth 2007). -
Adaptability to Submerged Culture and Amtno Acid Contents of Certain Fleshy Fungi Common in Finland
Adaptability to submerged culture and amtno acid contents of certain fleshy fungi common in Finland Mar j a L i is a H a t t u l a and H . G. G y ll e n b e r g Department of Microbiology, University of Helsinki, Finland The literature on the possibilities of sub must be considered when the suitability of merged culture of macrofungi is already fungi for submerged production is evaluated. voluminous. However, the interest has merely The present work concerns a collection of been restricted to the traditionally most va fungi common in Finland which have been lued fungi, particularly members of the gene investigated according to the criteria descri ra Agaricus and M orchella (HuMFELD, 1948, bed above. 1952, HuMFELD & SuGIHARA, 1949, 1952, Su GIHARA & HuMFELD, 1954, SzuEcs 1956, LITCHFIELD, 1964, 1967 a, b, LITCHFIELD & al., MATERIAL 1963) . The information obtainable from stu dies on these organisms is not especially en The material consisted of 33 species of fun couraging because the rate of biomass pro gi, 29 of which were obtained from the duction seems to be too low to compete fa Department of Silviculture, University of ,·ourably with other alternatives of single cell Helsinki, through the courtesy of Professor P. protein production (LITCHFIELD, 1967 a, b). Mikola and Mr. 0 . Laiho. Four species were On the other hand, the traditional use of fun isolated by the present authors by taking a gi as human food all over the world is a sterile piece of the fruiting body at the point significant reason for continued research on where the cap and the stem are joined and the submerged production o.f fungal mycel by transferring it on a slant of suitable agar. -
Lichens and Associated Fungi from Glacier Bay National Park, Alaska
The Lichenologist (2020), 52,61–181 doi:10.1017/S0024282920000079 Standard Paper Lichens and associated fungi from Glacier Bay National Park, Alaska Toby Spribille1,2,3 , Alan M. Fryday4 , Sergio Pérez-Ortega5 , Måns Svensson6, Tor Tønsberg7, Stefan Ekman6 , Håkon Holien8,9, Philipp Resl10 , Kevin Schneider11, Edith Stabentheiner2, Holger Thüs12,13 , Jan Vondrák14,15 and Lewis Sharman16 1Department of Biological Sciences, CW405, University of Alberta, Edmonton, Alberta T6G 2R3, Canada; 2Department of Plant Sciences, Institute of Biology, University of Graz, NAWI Graz, Holteigasse 6, 8010 Graz, Austria; 3Division of Biological Sciences, University of Montana, 32 Campus Drive, Missoula, Montana 59812, USA; 4Herbarium, Department of Plant Biology, Michigan State University, East Lansing, Michigan 48824, USA; 5Real Jardín Botánico (CSIC), Departamento de Micología, Calle Claudio Moyano 1, E-28014 Madrid, Spain; 6Museum of Evolution, Uppsala University, Norbyvägen 16, SE-75236 Uppsala, Sweden; 7Department of Natural History, University Museum of Bergen Allégt. 41, P.O. Box 7800, N-5020 Bergen, Norway; 8Faculty of Bioscience and Aquaculture, Nord University, Box 2501, NO-7729 Steinkjer, Norway; 9NTNU University Museum, Norwegian University of Science and Technology, NO-7491 Trondheim, Norway; 10Faculty of Biology, Department I, Systematic Botany and Mycology, University of Munich (LMU), Menzinger Straße 67, 80638 München, Germany; 11Institute of Biodiversity, Animal Health and Comparative Medicine, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow G12 8QQ, UK; 12Botany Department, State Museum of Natural History Stuttgart, Rosenstein 1, 70191 Stuttgart, Germany; 13Natural History Museum, Cromwell Road, London SW7 5BD, UK; 14Institute of Botany of the Czech Academy of Sciences, Zámek 1, 252 43 Průhonice, Czech Republic; 15Department of Botany, Faculty of Science, University of South Bohemia, Branišovská 1760, CZ-370 05 České Budějovice, Czech Republic and 16Glacier Bay National Park & Preserve, P.O. -
Full-Text (PDF)
African Journal of Microbiology Research Vol. 5(31), pp. 5750-5756, 23 December, 2011 Available online at http://www.academicjournals.org/AJMR ISSN 1996-0808 ©2011 Academic Journals DOI: 10.5897/AJMR11.1228 Full Length Research Paper Leucocalocybe, a new genus for Tricholoma mongolicum (Agaricales, Basidiomycota) Xiao-Dan Yu1,2, Hui Deng1 and Yi-Jian Yao1,3* 1State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, China. 2Graduate University of Chinese Academy of Sciences, Beijing, 100049, China. 3Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3AB, United Kingdom. Accepted 11 November, 2011 A new genus of Agaricales, Leucocalocybe was erected for a species Tricholoma mongolicum in this study. Leucocalocybe was distinguished from the other genera by a unique combination of macro- and micro-morphological characters, including a tricholomatoid habit, thick and short stem, minutely spiny spores and white spore print. The assignment of the new genus was supported by phylogenetic analyses based on the LSU sequences. The results of molecular analyses demonstrated that the species was clustered in tricholomatoid clade, which formed a distinct lineage. Key words: Agaricales, taxonomy, Tricholoma, tricholomatoid clade. INTRODUCTION The genus Tricholoma (Fr.) Staude is typified by having were re-described. Based on morphological and mole- distinctly emarginate-sinuate lamellae, white or very pale cular analyses, T. mongolicum appears to be aberrant cream spore print, producing smooth thin-walled within Tricholoma and un-subsumable into any of the basidiospores, lacking clamp connections, cheilocystidia extant genera. Accordingly, we proposed to erect a new and pleurocystidia (Singer, 1986). Most species of this genus, Leucocalocybe, to circumscribe the unique genus form obligate ectomycorrhizal associations with combination of features characterizing this fungus and a forest trees, only a few species in the subgenus necessary new combination. -
Biodiversity of Dead Wood
Scottish Natural Heritage Biodiversity of Dead Wood Fungi – Lichens - Bryophytes Dr David Genney SNH Policy and Advice Officer Scottish Natural Heritage Key messages Scotland is home to thousands of fungi, lichens and bryophytes, many of which depend on dead wood as a food source or place to grow. This presentation gives a brief introduction, for each group, to the diversity of dead wood species and the types of dead wood they need to survive. The take-home message is that the dead wood habitat is as diverse as the species that depend upon it. Ensuring a wide range of these dead wood types will maximise species diversity. Some dead wood types need special management and may need to be prioritised in areas where threatened species depend upon them. Scottish Natural Heritage FUNGI Dead wood is food for fungi and they, in turn, have a big impact on its quality and ultimate fate With thousands of species, each with specific habitat requirements, fungi require a wide diversity of dead wood types to maximise diversity Liz Holden Scottish Natural Heritage Different fungi rot wood in different ways – the main types of rot are brown rot and white rot Brown rot fungi The main building block of wood, cellulose, is broken down by the fungi, but not other structural compounds such as lignin. Dead wood is brown and exhibits brick-like cracking Many bracket fungi are brown rotters Liz Holden Cellulose Scottish Natural Heritage White-rot fungi White-rot fungi degrade a wider range of wood compounds, including the very complex polymer, lignin Pale wood More species are white-rot than brown-rot fungi Lignin Liz Holden Lignin Scottish Natural Heritage Armillaria spp.