New and Interesting Lichen Records from Northeastern Poland
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Key to the Species of Agonimia (Lichenised Ascomycota, Verrucariaceae)
Österr. Z. Pilzk. 28 (2019) – Austrian J. Mycol. 28 (2019, publ. 2020) 69 Key to the species of Agonimia (lichenised Ascomycota, Verrucariaceae) OTHMAR BREUSS Naturhistorisches Museum Wien, Botanische Abteilung (Kryptogamenherbar) Burgring 7 1010 Wien, Österreich E-Mail: [email protected] Accepted 29. September 2020. © Austrian Mycological Society, published online 25. October 2020 BREUSS, O., 2020: Key to the species of Agonimia (lichenised Ascomycota, Verrucariaceae). – Österr. Z. Pilzk. 28: 69–74. Key words: Pyrenocarpous lichens, Verrucariales, Agonimia, Agonimiella, Flakea. – Taxonomy, key. Abstract: A key to the 24 Agonimia species presently known is provided. A short survey of relevant literature on the genus and its affinities is added. Zusammenfassung: Ein Bestimmungsschlüssel zu den 24 bisher bekannten Agonimia-Arten wird vor- gelegt. Eine kurze Übersicht über relevante Literatur zur Gattung und ihrer Verwandtschaft ist beigefügt. Agonimia ZAHLBR. was introduced by ZAHLBRUCKNER (1909) for Agonimia tristicula (NYL.) ZAHLBR. and his newly described A. latzelii ZAHLBR. (now included within A. tristicula). It was not earlier than 1978 that another species was added to the genus: A. octospora (COPPINS & JAMES 1978). Later a handful of species previously treated in other genera (Polyblastia MASSAL., Physcia (SCHREB.) MICHX., Omphalina QUÉL.) have been transferred to Agonimia (COPPINS & al. 1992, VĚZDA 1997, SÉRUSIAUX & al. 1999, LÜCKING & MONCADA 2017, NIMIS & al. 2018). A couple of additional species have been described as new quite recently (SÉRUSIAUX & al. 1999; CZARNOTA & COP- PINS 2000; KASHIWADANI 2008; DYMYTROVA & al. 2011; GUZOW-KRZEMIŃSKA & al. 2012; APTROOT & CÁCERES 2013; HARADA 2013; KONDRATYUK 2015; KONDRATYUK & al. 2015, 2016, 2018; MCCARTHY & ELIX 2018). The circumscription of Agonimia is not fully clear. -
BLS Bulletin 111 Winter 2012.Pdf
1 BRITISH LICHEN SOCIETY OFFICERS AND CONTACTS 2012 PRESIDENT B.P. Hilton, Beauregard, 5 Alscott Gardens, Alverdiscott, Barnstaple, Devon EX31 3QJ; e-mail [email protected] VICE-PRESIDENT J. Simkin, 41 North Road, Ponteland, Newcastle upon Tyne NE20 9UN, email [email protected] SECRETARY C. Ellis, Royal Botanic Garden, 20A Inverleith Row, Edinburgh EH3 5LR; email [email protected] TREASURER J.F. Skinner, 28 Parkanaur Avenue, Southend-on-Sea, Essex SS1 3HY, email [email protected] ASSISTANT TREASURER AND MEMBERSHIP SECRETARY H. Döring, Mycology Section, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3AB, email [email protected] REGIONAL TREASURER (Americas) J.W. Hinds, 254 Forest Avenue, Orono, Maine 04473-3202, USA; email [email protected]. CHAIR OF THE DATA COMMITTEE D.J. Hill, Yew Tree Cottage, Yew Tree Lane, Compton Martin, Bristol BS40 6JS, email [email protected] MAPPING RECORDER AND ARCHIVIST M.R.D. Seaward, Department of Archaeological, Geographical & Environmental Sciences, University of Bradford, West Yorkshire BD7 1DP, email [email protected] DATA MANAGER J. Simkin, 41 North Road, Ponteland, Newcastle upon Tyne NE20 9UN, email [email protected] SENIOR EDITOR (LICHENOLOGIST) P.D. Crittenden, School of Life Science, The University, Nottingham NG7 2RD, email [email protected] BULLETIN EDITOR P.F. Cannon, CABI and Royal Botanic Gardens Kew; postal address Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3AB, email [email protected] CHAIR OF CONSERVATION COMMITTEE & CONSERVATION OFFICER B.W. Edwards, DERC, Library Headquarters, Colliton Park, Dorchester, Dorset DT1 1XJ, email [email protected] CHAIR OF THE EDUCATION AND PROMOTION COMMITTEE: S. -
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. -
A Higher-Level Phylogenetic Classification of the Fungi
mycological research 111 (2007) 509–547 available at www.sciencedirect.com journal homepage: www.elsevier.com/locate/mycres A higher-level phylogenetic classification of the Fungi David S. HIBBETTa,*, Manfred BINDERa, Joseph F. BISCHOFFb, Meredith BLACKWELLc, Paul F. CANNONd, Ove E. ERIKSSONe, Sabine HUHNDORFf, Timothy JAMESg, Paul M. KIRKd, Robert LU¨ CKINGf, H. THORSTEN LUMBSCHf, Franc¸ois LUTZONIg, P. Brandon MATHENYa, David J. MCLAUGHLINh, Martha J. POWELLi, Scott REDHEAD j, Conrad L. SCHOCHk, Joseph W. SPATAFORAk, Joost A. STALPERSl, Rytas VILGALYSg, M. Catherine AIMEm, Andre´ APTROOTn, Robert BAUERo, Dominik BEGEROWp, Gerald L. BENNYq, Lisa A. CASTLEBURYm, Pedro W. CROUSl, Yu-Cheng DAIr, Walter GAMSl, David M. GEISERs, Gareth W. GRIFFITHt,Ce´cile GUEIDANg, David L. HAWKSWORTHu, Geir HESTMARKv, Kentaro HOSAKAw, Richard A. HUMBERx, Kevin D. HYDEy, Joseph E. IRONSIDEt, Urmas KO˜ LJALGz, Cletus P. KURTZMANaa, Karl-Henrik LARSSONab, Robert LICHTWARDTac, Joyce LONGCOREad, Jolanta MIA˛ DLIKOWSKAg, Andrew MILLERae, Jean-Marc MONCALVOaf, Sharon MOZLEY-STANDRIDGEag, Franz OBERWINKLERo, Erast PARMASTOah, Vale´rie REEBg, Jack D. ROGERSai, Claude ROUXaj, Leif RYVARDENak, Jose´ Paulo SAMPAIOal, Arthur SCHU¨ ßLERam, Junta SUGIYAMAan, R. Greg THORNao, Leif TIBELLap, Wendy A. UNTEREINERaq, Christopher WALKERar, Zheng WANGa, Alex WEIRas, Michael WEISSo, Merlin M. WHITEat, Katarina WINKAe, Yi-Jian YAOau, Ning ZHANGav aBiology Department, Clark University, Worcester, MA 01610, USA bNational Library of Medicine, National Center for Biotechnology Information, -
Piedmont Lichen Inventory
PIEDMONT LICHEN INVENTORY: BUILDING A LICHEN BIODIVERSITY BASELINE FOR THE PIEDMONT ECOREGION OF NORTH CAROLINA, USA By Gary B. Perlmutter B.S. Zoology, Humboldt State University, Arcata, CA 1991 A Thesis Submitted to the Staff of The North Carolina Botanical Garden University of North Carolina at Chapel Hill Advisor: Dr. Johnny Randall As Partial Fulfilment of the Requirements For the Certificate in Native Plant Studies 15 May 2009 Perlmutter – Piedmont Lichen Inventory Page 2 This Final Project, whose results are reported herein with sections also published in the scientific literature, is dedicated to Daniel G. Perlmutter, who urged that I return to academia. And to Theresa, Nichole and Dakota, for putting up with my passion in lichenology, which brought them from southern California to the Traingle of North Carolina. TABLE OF CONTENTS Introduction……………………………………………………………………………………….4 Chapter I: The North Carolina Lichen Checklist…………………………………………………7 Chapter II: Herbarium Surveys and Initiation of a New Lichen Collection in the University of North Carolina Herbarium (NCU)………………………………………………………..9 Chapter III: Preparatory Field Surveys I: Battle Park and Rock Cliff Farm……………………13 Chapter IV: Preparatory Field Surveys II: State Park Forays…………………………………..17 Chapter V: Lichen Biota of Mason Farm Biological Reserve………………………………….19 Chapter VI: Additional Piedmont Lichen Surveys: Uwharrie Mountains…………………...…22 Chapter VII: A Revised Lichen Inventory of North Carolina Piedmont …..…………………...23 Acknowledgements……………………………………………………………………………..72 Appendices………………………………………………………………………………….…..73 Perlmutter – Piedmont Lichen Inventory Page 4 INTRODUCTION Lichens are composite organisms, consisting of a fungus (the mycobiont) and a photosynthesising alga and/or cyanobacterium (the photobiont), which together make a life form that is distinct from either partner in isolation (Brodo et al. -
AUSTRALASIAN LICHENOLOGY 83, July 2018 AUSTRALASIAN
The striking red pigments in the apothecia of species of Haematomma are concentrated mostly in the epihymenium above the tips of the asci. In this Haematomma persoonii the pigment is a tetracyclic anthraquinone called russulone. The compound has been found in the epihymenia of eight of Australia’s 13 known species of the genus. Haematomma persoonii colonizes bark in the woodlands and forests of eastern Queensland and New South Wales in Australia. Elsewhere in the world it occurs in all of the Americas, plus several sites in Africa and the Pacific. 1 mm CONTENTS ARTICLES Elix, JA; Mayrhofer, H; Rodriguez, JM—Two new species, a new combination and four new records of saxicolous buellioid lichens (Ascomycota, Caliciaceae) from southern South America ............................................................................................... 3 McCarthy, PM; Elix, JA—Sclerophyton puncticulatum sp. nov. (lichenized Ascomy- cota, Opegraphaceae) from New South Wales, Australia...................................... 14 McCarthy, PM; Elix, JA—Agonimia abscondita sp. nov. (lichenized Ascomycota, Verrucariaceae) from New South Wales, Australia ................................................ 18 Mayrhofer, H; Elix, JA—A new species of Rinodina (Physciaceae, Ascomycota) from eastern Australia ................................................................................................ 22 Elix, JA—A key to the buellioid lichens (Ascomycota, Caliciaceae) in New Zea- land ............................................................................................................................... -
Performance of Four Ribosomal DNA Regions to Infer Higher-Level Phylogenetic Relationships of Inoperculate Euascomycetes (Leotiomyceta)
Molecular Phylogenetics and Evolution 34 (2005) 512–524 www.elsevier.com/locate/ympev Performance of four ribosomal DNA regions to infer higher-level phylogenetic relationships of inoperculate euascomycetes (Leotiomyceta) H. Thorsten Lumbscha,¤, Imke Schmitta, Ralf Lindemuthb, Andrew Millerc, Armin Mangolda,b, Fernando Fernandeza, Sabine Huhndorfa a Department of Botany, The Field Museum, 1400 S. Lake Shore Drive, Chicago, IL 60605, USA b Universität Duisburg-Essen, Campus Essen, 45117 Essen, Germany c Center for Biodiversity, Illinois Natural History Survey, 607 E. Peabody Drive, Champaign, IL 61820, USA Received 9 June 2004; revised 14 October 2004 Available online 1 January 2005 Abstract The inoperculate euascomycetes are Wlamentous fungi that form saprobic, parasitic, and symbiotic associations with a wide vari- ety of animals, plants, cyanobacteria, and other fungi. The higher-level relationships of this economically important group have been unsettled for over 100 years. A data set of 55 species was assembled including sequence data from nuclear and mitochondrial small and large subunit rDNAs for each taxon; 83 new sequences were obtained for this study. Parsimony and Bayesian analyses were per- formed using the four-region data set and all 14 possible subpartitions of the data. The mitochondrial LSU rDNA was used for the Wrst time in a higher-level phylogenetic study of ascomycetes and its use in concatenated analyses is supported. The classes that were recognized in Leotiomyceta ( D inoperculate euascomycetes) in a classiWcation by Eriksson and Winka [Myconet 1 (1997) 1] are strongly supported as monophyletic. The following classes formed strongly supported sister-groups: Arthoniomycetes and Doth- ideomycetes, Chaetothyriomycetes and Eurotiomycetes, and Leotiomycetes and Sordariomycetes. -
High-Level Classification of the Fungi and a Tool for Evolutionary Ecological Analyses
Fungal Diversity (2018) 90:135–159 https://doi.org/10.1007/s13225-018-0401-0 (0123456789().,-volV)(0123456789().,-volV) High-level classification of the Fungi and a tool for evolutionary ecological analyses 1,2,3 4 1,2 3,5 Leho Tedersoo • Santiago Sa´nchez-Ramı´rez • Urmas Ko˜ ljalg • Mohammad Bahram • 6 6,7 8 5 1 Markus Do¨ ring • Dmitry Schigel • Tom May • Martin Ryberg • Kessy Abarenkov Received: 22 February 2018 / Accepted: 1 May 2018 / Published online: 16 May 2018 Ó The Author(s) 2018 Abstract High-throughput sequencing studies generate vast amounts of taxonomic data. Evolutionary ecological hypotheses of the recovered taxa and Species Hypotheses are difficult to test due to problems with alignments and the lack of a phylogenetic backbone. We propose an updated phylum- and class-level fungal classification accounting for monophyly and divergence time so that the main taxonomic ranks are more informative. Based on phylogenies and divergence time estimates, we adopt phylum rank to Aphelidiomycota, Basidiobolomycota, Calcarisporiellomycota, Glomeromycota, Entomoph- thoromycota, Entorrhizomycota, Kickxellomycota, Monoblepharomycota, Mortierellomycota and Olpidiomycota. We accept nine subkingdoms to accommodate these 18 phyla. We consider the kingdom Nucleariae (phyla Nuclearida and Fonticulida) as a sister group to the Fungi. We also introduce a perl script and a newick-formatted classification backbone for assigning Species Hypotheses into a hierarchical taxonomic framework, using this or any other classification system. We provide an example -
Phylogeny and Taxonomy of Polyblastia and Allied Taxa (Verrucariaceae)
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 370 Phylogeny and Taxonomy of Polyblastia and allied taxa (Verrucariaceae) ´ SANJA SAVIC ACTA UNIVERSITATIS UPSALIENSIS ISSN 1651-6214 UPPSALA ISBN 978-91-554-7035-7 2007 urn:nbn:se:uu:diva-8326 ! " # $%%& %'%% ( ( ( ) * + , * -. -* $%%&* ) + ( /01* ! * 2&%* 22 * * 3- 4& 54566#5&%265&* !* 7* ( 8 ( 0 /! 1* + ( (, ( , * ! 9 ( - ( : ; , 0 , ( * ! < / 3+-1 , , : ;* + * 8 * + ( * 3 (( ( ! =! * " ( ( , * + * - , , (( * ! ( > ! , , * ! < * ! ( ( 0 (( * + , /! # 1 * - ( ( , (( ( * + ( ( ( ( * + , $ /01 , $ $ $ * ! ( < ( * %&' ) 0 - ! + 0 - + ) + 3+- - ?) ( )* + * , * * - ./ * * +012345 * & @ - > -. $%%& 3-- A65A$# 3- 4& 54566#5&%265& ' ''' 5 2$A / '== *<*= B C ' ''' 5 2$A1 List of papers This thesis is based on the following papers, which are referred to in the text by their Roman numerals: I Savi Sanja, Tibell Leif, Gueidan Cécile & Lutzoni François. Molecular Phylogeny and Systematics of Polyblastia (Verrucari- aceae, Eurotiomycetes) and allied genera. Submitted -
Opuscula Philolichenum, 11: 120-XXXX
Opuscula Philolichenum, 12: 198-232. 2013. *pdf effectively published online 11December2013 via (http://sweetgum.nybg.org/philolichenum/) Lichens of the Bruce Peninsula, Ontario: Results from the 17th Tuckerman Workshop, 18-22 Sept. 2008 1 2 3 4 5 IRWIN M. BRODO , RICHARD C. HARRIS , WILLIAM BUCK , JAMES C. LENDEMER , CHRIS LEWIS , ABSTRACT. – An inventory of the lichens of Bruce Peninsula National Park and Fathom Five National Marine Park in the Georgian Bay area of southern Ontario was carried out by 30 lichenologists participating in the 2008 Tuckerman Workshop. A list of 370 species of lichens, related fungi and lichenicolous fungi was compiled, documenting that the parks are remarkably rich in lichens, including many rarities. Following the park inventory, an additional 21 lichens from Bruce County are listed based on the published literature and other recent collections. Twelve lichens, one related fungus and nine lichenicolous fungi are additions to the Canadian lichen flora: Acarospora moenium, Bagliettoa baldensis, Biatora ocelliformis, Caloplaca flavocitrina, Clavascidium umbrinum, Dermatocarpon dolomiticum, D. muhlenbergii, Heppia adglutinata, Lecania cuprea, Opegrapha mougeotii, Thelidium minutulum, Heteroplacidium compactum; Mycoglaena myricae; Capronia peltigerae, Lichenoconium erodens, Muellerella hospitans, M. ventosicola, Phaeopyxis punctum, Phoma cladoniicola, Plectocarpon cladoniae, Polycoccum minutulum, Tremella candelariellae. An additional 35 lichens, two related fungi, and 13 lichenicolous fungi are new for Ontario: Acarospora macrospora, Biatora chrysantha, B. turgidula, Biatorella hemisphaerica, Botryolepraria lesdainii, Buellia griseovirens, Caloplaca saxicola, C. subsoluta, Cladonia atlantica, Clauzadea monticola, Cliostomum leprosum, Diplotomma venustum, Enterographa zonata, Farnoldia hypocrita, Gyalecta foveolaris, Hymenelia heteromorpha, Lempholemma isidiodes, Lepraria caesiella, L. eburnea, Leptogium intermedium, Opegrapha rufescens, Placidium squamulosum, Porpidia contraponenda, P. macrocarpa f. -
Using a Multigene Phylogenetic Analysis to Assess Generic Delineation and Character Evolution in Verrucariaceae (Verrucariales, Ascomycota)
mycological research 111 (2007) 1145–1168 journal homepage: www.elsevier.com/locate/mycres Using a multigene phylogenetic analysis to assess generic delineation and character evolution in Verrucariaceae (Verrucariales, Ascomycota) Ce´cile GUEIDANa,*, Claude ROUXb, Franc¸ois LUTZONIa aDuke University, Department of Biology, Durham, NC 27708-0338, USA bChemin des Vignes Vieilles, 84120 Mirabeau, France article info abstract Article history: Verrucariaceae are a family of mostly crustose lichenized ascomycetes colonizing various Received 3 February 2007 habitats ranging from marine and fresh water to arid environments. Phylogenetic relation- Received in revised form ships among members of the Verrucariaceae are mostly unknown and the current morphol- 28 May 2007 ogy-based classification has never been confronted to molecular data. A multilocus Accepted 13 August 2007 phylogeny (nuLSU, nuSSU and RPB1) was reconstructed for 83 taxa representing all main Published online 26 August 2007 genera of this family to provide a molecular phylogenetic framework necessary to assess Corresponding Editor: Martin Grube the current morphology-based classification. Four main well-supported monophyletic groups were recovered, one of which contains seven robust monophyletic subgroups. Keywords: Most genera, as traditionally delimited, were not monophyletic. A few taxonomic changes Ancestral state reconstruction are proposed here to reconcile the morphology-based classification with the molecular Lichen-forming fungi phylogeny (Endocarpon diffractellum comb. nov., -
Muggia 2020 Plant and Fungal Systematics
© 2019 W. Szafer Institute of Botany Polish Academy of Sciences Plant and Fungal Systematics 64(2): 367–381, 2019 ISSN 2544-7459 (print) DOI: 10.2478/pfs-2019-0024 ISSN 2657-5000 (online) Muellerella, a lichenicolous fungal genus recovered as polyphyletic within Chaetothyriomycetidae (Eurotiomycetes, Ascomycota) Lucia Muggia1*, Sergio Pérez-Ortega2 & Damien Ertz3,4 Abstract. Molecular data and culture-dependent methods have helped to uncover the Article info phylogenetic relationships of numerous species of lichenicolous fungi, a specialized group Received: 2 May 2019 of taxa that inhabit lichens and have developed diverse degrees of specificity and parasitic Revision received: 20 Jul. 2019 behaviors. The majority of lichenicolous fungal taxa are known in either their anamorphic or Accepted: 20 Jul. 2019 Published: 2 Dec. 2019 teleomorphic states, although their anamorph-teleomorph relationships have been resolved in only a few cases. The pycnidium-forming Lichenodiplis lecanorae and the perithecioid taxa Associate Editor Muellerella atricola and M. lichenicola were recently recovered as monophyletic in Chae- Paul Diederich tothyriales (Eurotiomycetes). Both genera are lichenicolous on multiple lichen hosts, upon which they show a subtle morphological diversity reflected in the description of 14 species in Muellerella (of which 12 are lichenicolous) and 12 in Lichenodiplis. Here we focus on the teleomorphic genus Muellerella and investigate its monophyly by expanding the taxon sampling to other species occurring on diverse lichen hosts. We generated molecular data for two nuclear and one mitochondrial loci (28S, 18S and 16S) from environmental samples. The present multilocus phylogeny confirms the monophyletic lineage of the teleomorphic M. atricola and M. lichenicola with their L.