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Phylogeny of the Cetrarioid Core (Parmeliaceae) Based on Five
The Lichenologist 41(5): 489–511 (2009) © 2009 British Lichen Society doi:10.1017/S0024282909990090 Printed in the United Kingdom Phylogeny of the cetrarioid core (Parmeliaceae) based on five genetic markers Arne THELL, Filip HÖGNABBA, John A. ELIX, Tassilo FEUERER, Ingvar KÄRNEFELT, Leena MYLLYS, Tiina RANDLANE, Andres SAAG, Soili STENROOS, Teuvo AHTI and Mark R. D. SEAWARD Abstract: Fourteen genera belong to a monophyletic core of cetrarioid lichens, Ahtiana, Allocetraria, Arctocetraria, Cetraria, Cetrariella, Cetreliopsis, Flavocetraria, Kaernefeltia, Masonhalea, Nephromopsis, Tuckermanella, Tuckermannopsis, Usnocetraria and Vulpicida. A total of 71 samples representing 65 species (of 90 worldwide) and all type species of the genera are included in phylogentic analyses based on a complete ITS matrix and incomplete sets of group I intron, -tubulin, GAPDH and mtSSU sequences. Eleven of the species included in the study are analysed phylogenetically for the first time, and of the 178 sequences, 67 are newly constructed. Two phylogenetic trees, one based solely on the complete ITS-matrix and a second based on total information, are similar, but not entirely identical. About half of the species are gathered in a strongly supported clade composed of the genera Allocetraria, Cetraria s. str., Cetrariella and Vulpicida. Arctocetraria, Cetreliopsis, Kaernefeltia and Tuckermanella are monophyletic genera, whereas Cetraria, Flavocetraria and Tuckermannopsis are polyphyletic. The taxonomy in current use is compared with the phylogenetic results, and future, probable or potential adjustments to the phylogeny are discussed. The single non-DNA character with a strong correlation to phylogeny based on DNA-sequences is conidial shape. The secondary chemistry of the poorly known species Cetraria annae is analyzed for the first time; the cortex contains usnic acid and atranorin, whereas isonephrosterinic, nephrosterinic, lichesterinic, protolichesterinic and squamatic acids occur in the medulla. -
Genetic Variation Within and Among Populations of the Threatened Lichen Lobaria Pulmonaria in Switzerland and Implications for I
MEC820.fm Page 2049 Saturday, December 18, 1999 1:20 PM Molecular Ecology (1999) 8, 2049–2059 GeneticBlackwell Science, Ltd variation within and among populations of the threatened lichen Lobaria pulmonaria in Switzerland and implications for its conservation S. ZOLLER,* F. LUTZONI† and C. SCHEIDEGGER* *Swiss Federal Institute for Forest, Snow and Landscape Research, CH-8903 Birmensdorf, Switzerland, †Department of Botany, The Field Museum of Natural History, Chicago IL 60605, USA Abstract The foliose epiphytic lichen Lobaria pulmonaria has suffered a significant decline in European lowlands during the last decades and therefore is considered as endangered throughout Europe. An assessment of the genetic variability is necessary to formulate biologically sound conservation recommendations for this species. We investigated the genetic diversity of the fungal symbiont of L. pulmonaria using 143 specimens sampled from six populations (two small, one medium, three large) in the lowland, the Jura Moun- tains, the pre-Alps and the Alps of Switzerland. Among all nuclear and mitochondrial regions sequenced for this study, variability was found only in the internal transcribed spacer (ITS I), with three polymorphic sites, and in the nuclear ribosomal large subunit (nrLSU), with four polymorphic sites. The variable sites in the nrLSU are all located within a putative spliceosomal intron. We sequenced these two regions for 81 specimens and detected six genotypes. Two genotypes were common, two were found only in the more diverse populations and two were found only in one population each. There was no correlation between population size and genetic diversity. The highest genetic diversity was found in populations where the fungal symbiont is reproducing sexually. -
Four <I>Parmeliaceae</I> Species Excluded from <I>Bulbothrix</I>
MYCOTAXON Volume 111, pp. 387–401 January–March 2010 Four Parmeliaceae species excluded from Bulbothrix Michel N. Benatti1 & Marcelo P. Marcelli2 1 [email protected] & 2 [email protected] Instituto de Botânica, Seção de Micologia e Liquenologia Caixa Postal 3005, São Paulo/SP, CEP 01061-970, Brazil Abstract — Four species previously included in the genus Bulbothrix are shown not to form bulbate cilia and are combined into alternative genera as Hypotrachyna tuskiformis, Parmelinopsis pinguiacida, P. subinflata, and Parmotrema yunnanum. All species are described in detail and a lectotype is selected for Bulbothrix tuskiformis. Key words — Bulbothrix pinguiacida, Bulbothrix subinflata, Bulbothrix yunnana Introduction The genus Bulbothrix Hale was proposed for a group of species previously included in Parmelia ser. Bicornutae (Lynge) Hale & Kurokawa (Hale 1974) characterized by small laciniate, adnate thalli, bulbate marginal cilia, cortical atranorin, simple to branched cilia and rhizines, smooth to coronate apothecia, unicellular, colorless, ellipsoid to bicornute ascospores 5−21 × 4−12 μm, and small, bacilliform to bifusiform conidia 5−10 µm long (Hale 1976b, Elix 1993a). During a taxonomic revision of the genus we found four species previously included in Bulbothrix that do not have the typical cilia with hollow basal bulbae that contain differentiated cells and an oily substance (Hale 1975, Feuerer & Marth 1997) should be classified outside this genus. These four species are distributed in Southeast Asia and Oceania. Hypotrachyna tuskiformis is still only known from the type locality in Papua New Guinea (Elix 1997b), Parmelinopsis pinguiacida from New Caledonia and Rarotonga (Louwhoff & Elix 2000a, 2000b), Parmelinopsis subinflata from the Philippines, Australia, Malaysia, and Papua New Guinea (Hale 1965, 1976b, Sipman 1993, Streimann 1986), and Parmotrema yunnanum from southern China (Wang et al. -
The Puzzle of Lichen Symbiosis
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 1503 The puzzle of lichen symbiosis Pieces from Thamnolia IOANA ONUT, -BRÄNNSTRÖM ACTA UNIVERSITATIS UPSALIENSIS ISSN 1651-6214 ISBN 978-91-554-9887-0 UPPSALA urn:nbn:se:uu:diva-319639 2017 Dissertation presented at Uppsala University to be publicly examined in Lindhalsalen, EBC, Norbyvägen 14, Uppsala, Thursday, 1 June 2017 at 09:15 for the degree of Doctor of Philosophy. The examination will be conducted in English. Faculty examiner: Associate Professor Anne Pringle (University of Wisconsin-Madison, Department of Botany). Abstract Onuț-Brännström, I. 2017. The puzzle of lichen symbiosis. Pieces from Thamnolia. Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 1503. 62 pp. Uppsala: Acta Universitatis Upsaliensis. ISBN 978-91-554-9887-0. Symbiosis brought important evolutionary novelties to life on Earth. Lichens, the symbiotic entities formed by fungi, photosynthetic organisms and bacteria, represent an example of a successful adaptation in surviving hostile environments. Yet many aspects of the lichen symbiosis remain unexplored. This thesis aims at bringing insights into lichen biology and the importance of symbiosis in adaptation. I am using as model system a successful colonizer of tundra and alpine environments, the worm lichens Thamnolia, which seem to only reproduce vegetatively through symbiotic propagules. When the genetic architecture of the mating locus of the symbiotic fungal partner was analyzed with genomic and transcriptomic data, a sexual self-incompatible life style was revealed. However, a screen of the mating types ratios across natural populations detected only one of the mating types, suggesting that Thamnolia has no potential for sexual reproduction because of lack of mating partners. -
Annotated Checklist of the Lichens and Lichenicolous Fungi of Bhutan
Fungal Diversity Annotated checklist of the lichens and lichenicolous fungi of Bhutan A. Aptroot1* and F.J. Feijen2 'Centraalbureau voor Schimmelcultures. P.O. Box 85167, NL-3508 AD Utrecht, The Netherlands 2Piet Heinlaan 5, NL-2341 SG Oegstgeest, The Netherlands Aptroot, A. and Feijen, FJ. (2002). Annotated checklist of the lichens and lichenicolous fungi of Bhutan. Fungal Diversity 11: 21-48. An annotated checklist is presented of the 287 lichens and lichenicolous fungi known from Bhutan. The vast majority (225) are new records for the country, based on recent collections of 264 species by the second author. Most species were previously known from the Himalayas, but some represent considerable range extensions. Noticeable examples are the rare Ropalospora chlorantha, so far only known from eastern North America, and the fITstreport from the Northern Hemisphere of Lepraria nigrocincta. Pyrrhospora bhutanensis is described as new to science. Key words: Bhutan, checklist, Himalaya, lichenicolous, lichens. Introduction The Kingdom of Bhutan is located in the eastern Himalayas. It stretches 300 kilometres from west to east, and about 150 kilometres from north to south. Bhutan has an extremely varied landscape, going from the high mountains (up to 7553 m) in the north to the lowland belt in the south (100-300 m altitude). A number of north-south running rivers created narrow valleys with each their own characteristics. The frontier between the Palaearctic and the Oriental biogeographical regions runs midway through the country. The country can be divided in three climatic zones: alpine, temperate and subtropical. Precipitation varies enormously within the country. In the subtropical south, monsoon rainfall reaches 5.5 m annually, while in the temperate foothills rainfall is moderate and both dry and wet valleys occur. -
Opuscula Philolichenum, 6: 1-XXXX
Opuscula Philolichenum, 15: 56-81. 2016. *pdf effectively published online 25July2016 via (http://sweetgum.nybg.org/philolichenum/) Lichens, lichenicolous fungi, and allied fungi of Pipestone National Monument, Minnesota, U.S.A., revisited M.K. ADVAITA, CALEB A. MORSE1,2 AND DOUGLAS LADD3 ABSTRACT. – A total of 154 lichens, four lichenicolous fungi, and one allied fungus were collected by the authors from 2004 to 2015 from Pipestone National Monument (PNM), in Pipestone County, on the Prairie Coteau of southwestern Minnesota. Twelve additional species collected by previous researchers, but not found by the authors, bring the total number of taxa known for PNM to 171. This represents a substantial increase over previous reports for PNM, likely due to increased intensity of field work, and also to the marked expansion of corticolous and anthropogenic substrates since the site was first surveyed in 1899. Reexamination of 116 vouchers deposited in MIN and the PNM herbarium led to the exclusion of 48 species previously reported from the site. Crustose lichens are the most common growth form, comprising 65% of the lichen diversity. Sioux Quartzite provided substrate for 43% of the lichen taxa collected. Saxicolous lichen communities were characterized by sampling four transects on cliff faces and low outcrops. An annotated checklist of the lichens of the site is provided, as well as a list of excluded taxa. We report 24 species (including 22 lichens and two lichenicolous fungi) new for Minnesota: Acarospora boulderensis, A. contigua, A. erythrophora, A. strigata, Agonimia opuntiella, Arthonia clemens, A. muscigena, Aspicilia americana, Bacidina delicata, Buellia tyrolensis, Caloplaca flavocitrina, C. lobulata, C. -
A New Species of Allocetraria (Parmeliaceae, Ascomycota) in China
The Lichenologist 47(1): 31–34 (2015) 6 British Lichen Society, 2015 doi:10.1017/S0024282914000528 A new species of Allocetraria (Parmeliaceae, Ascomycota) in China Rui-Fang WANG, Xin-Li WEI and Jiang-Chun WEI Abstract: Allocetraria yunnanensis R. F. Wang, X. L. Wei & J. C. Wei is described as a new species from the Yunnan Province of China, and is characterized by having a shiny upper surface, strongly wrinkled lower surface, and marginal pseudocyphellae present on the lower side in the form of a white continuous line or spot. The phylogenetic analysis based on nrDNA ITS sequences suggests that the new species is related to A. sinensis X. Q. Gao. Key words: Allocetraria yunnanensis, lichen, taxonomy Accepted for publication 26 June 2014 Introduction genus, as all ten species have been reported there (Kurokawa & Lai 1991; Thell et al. The lichenized genus Allocetraria Kurok. & 1995; Randlane et al. 2001; Wang et al. M. J. Lai was described in 1991, with a new 2014). During our taxonomic study of Allo- species A. isidiigera Kurok. & M. J. Lai, and cetraria, a new species was found. two new combinations: A. ambigua (C. Bab.) Kurok. & M. J. Lai and A. stracheyi (C. Bab.) Kurok. & M. J. Lai (Kurokawa & Lai 1991). The main distribution area of Allocetraria Materials and Methods species was reported to be in the Himalayas, A dissecting microscope (ZEISS Stemi SV11) and com- including China, India, and Nepal. pound microscope (ZEISS Axioskop 2 plus) were used Allocetraria is characterized by dichoto- to study the morphology and anatomy of the specimens. Colour test reagents [10% aqueous KOH, saturated mously or subdichotomously branched lobes aqueous Ca(OCl)2, and concentrated alcoholic p- and a foliose to suberect or erect thallus with phenylenediamine] and thin-layer chromatography sparse rhizines, angular to sublinear pseudo- (TLC, solvent system C) were used for the detection cyphellae, palisade plectenchymatous upper of lichen substances (Culberson & Kristinsson 1970; Culberson 1972). -
A Checklist of Lichens Collected During the First Howard Crum Bryological Workshop, Delaware Water Gap National Recreation Area
Opuscula Philolichenum, 2: 1-10. 2005. Contributions to the Lichen Flora of Pennsylvania: A Checklist of Lichens Collected During the First Howard Crum Bryological Workshop, Delaware Water Gap National Recreation Area RICHARD C. HARRIS1 & JAMES C. LENDEMER2 ABSTRACT. – A checklist of 209 species of lichens and lichenicolous fungi collected during the First Howard Crum Bryological Workshop in the Delaware Water Gap National Recreation Area, Pennsylvania, USA is provided. The new species Opegrapha bicolor R.C. Harris & Lendemer, collected during the Foray, is described. Chrysothrix flavovirens Tønsberg and Merismatium peregrinum (Flotow) Triebel are reported as new to North America. On April 23-26, 2004, we were graciously allowed to be commensals during the First Howard Crum Bryological Workshop in the Delaware Water Gap National Recreation Area, Pennsylvania, USA. Given the dearth of knowledge of lichen distributions in Pennsylvania and the overall lack of recent vouchers, this was a valuable opportunity to collect in what turned out to be a rich and interesting area. We were quite surprised by the apparent high lichen diversity, as well as the number of novelties and rarities, in an area so close to the East Coast megalopolis. In four half-days in the field, we collected 209 species in a limited area of the Pennsylvania part of the Park. Some are clearly new to science of which, Opegrapha bicolor is described here (see Endnote). Two presumably undescribed species of Fellhanera will be published elsewhere, and the Halecania will be included in a forthcoming treatment of Ozark lichens. Others are left for the future, as present material (and our knowledge) are inadequate. -
Mycosphere Notes 225–274: Types and Other Specimens of Some Genera of Ascomycota
Mycosphere 9(4): 647–754 (2018) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/9/4/3 Copyright © Guizhou Academy of Agricultural Sciences Mycosphere Notes 225–274: types and other specimens of some genera of Ascomycota Doilom M1,2,3, Hyde KD2,3,6, Phookamsak R1,2,3, Dai DQ4,, Tang LZ4,14, Hongsanan S5, Chomnunti P6, Boonmee S6, Dayarathne MC6, Li WJ6, Thambugala KM6, Perera RH 6, Daranagama DA6,13, Norphanphoun C6, Konta S6, Dong W6,7, Ertz D8,9, Phillips AJL10, McKenzie EHC11, Vinit K6,7, Ariyawansa HA12, Jones EBG7, Mortimer PE2, Xu JC2,3, Promputtha I1 1 Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand 2 Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, 132 Lanhei Road, Kunming 650201, China 3 World Agro Forestry Centre, East and Central Asia, 132 Lanhei Road, Kunming 650201, Yunnan Province, People’s Republic of China 4 Center for Yunnan Plateau Biological Resources Protection and Utilization, College of Biological Resource and Food Engineering, Qujing Normal University, Qujing, Yunnan 655011, China 5 Shenzhen Key Laboratory of Microbial Genetic Engineering, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, China 6 Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 7 Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiang Mai 50200, Thailand 8 Department Research (BT), Botanic Garden Meise, Nieuwelaan 38, BE-1860 Meise, Belgium 9 Direction Générale de l'Enseignement non obligatoire et de la Recherche scientifique, Fédération Wallonie-Bruxelles, Rue A. -
Three Challenges to Contemporaneous Taxonomy from a Licheno-Mycological Perspective
Megataxa 001 (1): 078–103 ISSN 2703-3082 (print edition) https://www.mapress.com/j/mt/ MEGATAXA Copyright © 2020 Magnolia Press Review ISSN 2703-3090 (online edition) https://doi.org/10.11646/megataxa.1.1.16 Three challenges to contemporaneous taxonomy from a licheno-mycological perspective ROBERT LÜCKING Botanischer Garten und Botanisches Museum, Freie Universität Berlin, Königin-Luise-Straße 6–8, 14195 Berlin, Germany �[email protected]; https://orcid.org/0000-0002-3431-4636 Abstract Nagoya Protocol, and does not need additional “policing”. Indeed, the Nagoya Protocol puts the heaviest burden on This paper discusses three issues that challenge contempora- taxonomy and researchers cataloguing biodiversity, whereas neous taxonomy, with examples from the fields of mycology for the intended target group, namely those seeking revenue and lichenology, formulated as three questions: (1) What is gain from nature, the protocol may not actually work effec- the importance of taxonomy in contemporaneous and future tively. The notion of currently freely accessible digital se- science and society? (2) An increasing methodological gap in quence information (DSI) to become subject to the protocol, alpha taxonomy: challenge or opportunity? (3) The Nagoya even after previous publication, is misguided and conflicts Protocol: improvement or impediment to the science of tax- with the guidelines for ethical scientific conduct. Through onomy? The importance of taxonomy in society is illustrated its implementation of the Nagoya Protocol, Colombia has using the example of popular field guides and digital me- set a welcome precedence how to exempt taxonomic and dia, a billion-dollar business, arguing that the desire to name systematic research from “access to genetic resources”, and species is an intrinsic feature of the cognitive component of hopefully other biodiversity-rich countries will follow this nature connectedness of humans. -
Mycologieycologie 2021 ● 42 ● 1 DIRECTEUR DE LA PUBLICATION / PUBLICATION DIRECTOR : Bruno DAVID Président Du Muséum National D’Histoire Naturelle
cryptogamie MMycologieycologie 2021 ● 42 ● 1 DIRECTEUR DE LA PUBLICATION / PUBLICATION DIRECTOR : Bruno DAVID Président du Muséum national d’Histoire naturelle RÉDACTEUR EN CHEF / EDITOR-IN-CHIEF : Bart BUYCK ASSISTANTE DE RÉDACTION / ASSISTANT EDITOR : Marianne SALAÜN ([email protected]) MISE EN PAGE / PAGE LAYOUT : Marianne SALAÜN RÉDACTEURS ASSOCIÉS / ASSOCIATE EDITORS : Slavomír ADAMČÍK Institute of Botany, Plant Science and Biodiversity Centre, Slovak Academy of Sciences, Dúbravská cesta 9, SK-84523, Bratislava (Slovakia) André APTROOT ABL Herbarium, G.v.d. Veenstraat 107, NL-3762 XK Soest (The Netherlands) Cony DECOCK Mycothèque de l’Université catholique de Louvain, Earth and Life Institute, Microbiology, Université catholique de Louvain, Croix du Sud 3, B-1348 Louvain-la-Neuve (Belgium) André FRAITURE Botanic Garden Meise, Domein van Bouchout, B-1860 Meise (Belgium) Kevin D. HYDE School of Science, Mae Fah Luang University, 333 M. 1 T.Tasud Muang District, Chiang Rai 57100 (Thailand) Valérie HOFSTETTER Station de recherche Agroscope Changins-Wädenswil, Dépt. Protection des plantes, Mycologie, CH-1260 Nyon 1 (Switzerland) Sinang HONGSANAN College of Life Science and Oceanography, Shenzhen University, 1068, Nanhai Avenue, Nanshan, ShenZhen 518055 (China) Egon HORAK Schlossfeld 17, A-6020 Innsbruck (Austria) Jing LUO Department of Plant Biology & Pathology, Rutgers University New Brunswick, NJ 08901 (United States) Ruvishika S. JAYAWARDENA Center of Excellence in Fungal Research, Mae Fah Luang University, 333 M. 1 T.Tasud Muang District, Chiang Rai 57100 (Thailand) Chen JIE Instituto de Ecología, Xalapa 91070, Veracruz (México) Sajeewa S.N. MAHARCHCHIKUMBURA Department of Crop Sciences, College of Agricultural and Marine Sciences, Sultan Qaboos University (Oman) Pierre-Arthur MOREAU UE 7144. -
Checklist of the Lichens and Allied Fungi of Kathy Stiles Freeland Bibb County Glades Preserve, Alabama, U.S.A
Opuscula Philolichenum, 18: 420–434. 2019. *pdf effectively published online 2December2019 via (http://sweetgum.nybg.org/philolichenum/) Checklist of the lichens and allied fungi of Kathy Stiles Freeland Bibb County Glades Preserve, Alabama, U.S.A. J. KEVIN ENGLAND1, CURTIS J. HANSEN2, JESSICA L. ALLEN3, SEAN Q. BEECHING4, WILLIAM R. BUCK5, VITALY CHARNY6, JOHN G. GUCCION7, RICHARD C. HARRIS8, MALCOLM HODGES9, NATALIE M. HOWE10, JAMES C. LENDEMER11, R. TROY MCMULLIN12, ERIN A. TRIPP13, DENNIS P. WATERS14 ABSTRACT. – The first checklist of lichenized, lichenicolous and lichen-allied fungi from the Kathy Stiles Freeland Bibb County Glades Preserve in Bibb County, Alabama, is presented. Collections made during the 2017 Tuckerman Workshop and additional records from herbaria and online sources are included. Two hundred and thirty-eight taxa in 115 genera are enumerated. Thirty taxa of lichenized, lichenicolous and lichen-allied fungi are newly reported for Alabama: Acarospora fuscata, A. novomexicana, Circinaria contorta, Constrictolumina cinchonae, Dermatocarpon dolomiticum, Didymocyrtis cladoniicola, Graphis anfractuosa, G. rimulosa, Hertelidea pseudobotryosa, Heterodermia pseudospeciosa, Lecania cuprea, Marchandiomyces lignicola, Minutoexcipula miniatoexcipula, Monoblastia rappii, Multiclavula mucida, Ochrolechia trochophora, Parmotrema subsumptum, Phaeographis brasiliensis, Phaeographis inusta, Piccolia nannaria, Placynthiella icmalea, Porina scabrida, Psora decipiens, Pyrenographa irregularis, Ramboldia blochiana, Thyrea confusa, Trichothelium