Life of Lichen
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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. -
Epiphytic Lichens and Lichenicolous Fungi From
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An Evolving Phylogenetically Based Taxonomy of Lichens and Allied Fungi
Opuscula Philolichenum, 11: 4-10. 2012. *pdf available online 3January2012 via (http://sweetgum.nybg.org/philolichenum/) An evolving phylogenetically based taxonomy of lichens and allied fungi 1 BRENDAN P. HODKINSON ABSTRACT. – A taxonomic scheme for lichens and allied fungi that synthesizes scientific knowledge from a variety of sources is presented. The system put forth here is intended both (1) to provide a skeletal outline of the lichens and allied fungi that can be used as a provisional filing and databasing scheme by lichen herbarium/data managers and (2) to announce the online presence of an official taxonomy that will define the scope of the newly formed International Committee for the Nomenclature of Lichens and Allied Fungi (ICNLAF). The online version of the taxonomy presented here will continue to evolve along with our understanding of the organisms. Additionally, the subfamily Fissurinoideae Rivas Plata, Lücking and Lumbsch is elevated to the rank of family as Fissurinaceae. KEYWORDS. – higher-level taxonomy, lichen-forming fungi, lichenized fungi, phylogeny INTRODUCTION Traditionally, lichen herbaria have been arranged alphabetically, a scheme that stands in stark contrast to the phylogenetic scheme used by nearly all vascular plant herbaria. The justification typically given for this practice is that lichen taxonomy is too unstable to establish a reasonable system of classification. However, recent leaps forward in our understanding of the higher-level classification of fungi, driven primarily by the NSF-funded Assembling the Fungal Tree of Life (AFToL) project (Lutzoni et al. 2004), have caused the taxonomy of lichen-forming and allied fungi to increase significantly in stability. This is especially true within the class Lecanoromycetes, the main group of lichen-forming fungi (Miadlikowska et al. -
The Macroevolutionary Dynamics of Symbiotic and Phenotypic Diversification in Lichens
The macroevolutionary dynamics of symbiotic and phenotypic diversification in lichens Matthew P. Nelsena,1, Robert Lückingb, C. Kevin Boycec, H. Thorsten Lumbscha, and Richard H. Reea aDepartment of Science and Education, Negaunee Integrative Research Center, The Field Museum, Chicago, IL 60605; bBotanischer Garten und Botanisches Museum, Freie Universität Berlin, 14195 Berlin, Germany; and cDepartment of Geological Sciences, Stanford University, Stanford, CA 94305 Edited by Joan E. Strassmann, Washington University in St. Louis, St. Louis, MO, and approved July 14, 2020 (received for review February 6, 2020) Symbioses are evolutionarily pervasive and play fundamental roles macroevolutionary consequences of ant–plant interactions (15–19). in structuring ecosystems, yet our understanding of their macroevo- However, insufficient attention has been paid to one of the most lutionary origins, persistence, and consequences is incomplete. We iconic examples of symbiosis (20, 21): Lichens. traced the macroevolutionary history of symbiotic and phenotypic Lichens are stable associations between a mycobiont (fungus) diversification in an iconic symbiosis, lichens. By inferring the most and photobiont (eukaryotic alga or cyanobacterium). The pho- comprehensive time-scaled phylogeny of lichen-forming fungi (LFF) tobiont supplies the heterotrophic fungus with photosynthetically to date (over 3,300 species), we identified shifts among symbiont derived carbohydrates, while the mycobiont provides the pho- classes that broadly coincided with the convergent -
Lichens of Alaska's South Coast
United States Department of Agriculture Lichens of Alaska’s South Coast Forest Service R10-RG-190 Alaska Region Reprint April 2014 WHAT IS A LICHEN? Lichens are specialized fungi that “farm” algae as a food source. Unlike molds, mildews, and mushrooms that parasitize or scavenge food from other organisms, the fungus of a lichen cultivates tiny algae and / or blue-green bacteria (called cyanobacteria) within the fabric of interwoven fungal threads that form the body of the lichen (or thallus). The algae and cyanobacteria produce food for themselves and for the fungus by converting carbon dioxide and water into sugars using the sun’s energy (photosynthesis). Thus, a lichen is a combination of two or sometimes three organisms living together. Perhaps the most important contribution of the fungus is to provide a protective habitat for the algae or cyanobacteria. The green or blue-green photosynthetic layer is often visible between two white fungal layers if a piece of lichen thallus is torn off. Most lichen-forming fungi cannot exist without the photosynthetic partner because they have become dependent on them for survival. But in all cases, a fungus looks quite different in the lichenized form compared to its free-living form. HOW DO LICHENS REPRODUCE? Lichens sexually reproduce with fruiting bodies of various shapes and colors that can often look like miniature mushrooms. These are called apothecia (Fig. 1) and contain spores that germinate and Figure 1. Apothecia, fruiting grow into the fungus. Each bodies fungus must find the right photosynthetic partner in order to become a lichen. Lichens reproduce asexually in several ways. -
Price's Scrub State Park
Price’s Scrub State Park Advisory Group Draft Unit Management Plan STATE OF FLORIDA DEPARTMENT OF ENVIRONMENTAL PROTECTION Division of Recreation and Parks September 2018 TABLE OF CONTENTS INTRODUCTION ...................................................................................1 PURPOSE AND SIGNIFICANCE OF THE PARK ....................................... 1 Park Significance ................................................................................1 PURPOSE AND SCOPE OF THE PLAN..................................................... 2 MANAGEMENT PROGRAM OVERVIEW ................................................... 7 Management Authority and Responsibility .............................................. 7 Park Management Goals ...................................................................... 8 Management Coordination ................................................................... 9 Public Participation ..............................................................................9 Other Designations .............................................................................9 RESOURCE MANAGEMENT COMPONENT INTRODUCTION ................................................................................. 11 RESOURCE DESCRIPTION AND ASSESSMENT..................................... 12 Natural Resources ............................................................................. 12 Topography .................................................................................. 12 Geology ...................................................................................... -
Komunitas Lumut Kerak (Lichens) Di Taman Wisata Alam Suranadi Kabupaten Lombok Barat
Komunitas Lumut Kerak (Lichens) Di Taman Wisata Alam Suranadi Kabupaten Lombok Barat Fitrianti*1, Faturrahman1, Sukiman1 1Department of Biology, Faculty of Mathematics and Natural Sciences, University of Mataram, Jl. Majapahit No. 62, Mataram 83125, West Nusa Tenggara, Indonesia Tlp/Fax. 0370 646506, email: *[email protected] Abstrak Lumut Kerak merupakan simbiosis antara fungi dan alga atau cyanobacterium. yang bermanfaat sebagai bioresource, biondikator serta studi ekosistem. Dalam penelitian ini, beberapa aspek lumut kerak akan diteliti meliputi komposisi jenis, beserta jumlah individu tiap jenisnya dan nilai keanekaragaman lumut kerak. Penelitian ini bersifat deskriptif eksploratif yang telah dilaksanakan pada bulan Oktober-Desember 2016. Pengambilan data dilakukan menggunakan metode stratified random sampling dengan menempatkan 11 unit sampel berbentuk persegi. Pada tiap unit sampel, dipilih 12 pohon yang masing-masing akan dipasang 4 grid berukuran 50x10 cm. Identifikasi sampel dilakukan dengan mencocokkan (profile matching) ciri morfologi serta hasil spot test dengan buku identifikasi. Nilai keanekaragaman lumut kerak dianalisis dengan menggunakan Lichen Diversity Value serta Indeks Shannon dan Pielou. Dari hasil penelitian, 4 spesies ditemukan dari kelas Lecanoromycetes dan kelas Arthoniomycetes. Satu spesies tidak teridentifikasi. Nilai LDVj tertinggi 13,5 dari unit sampel blok perlindungan. Indeks nilai Shannon sebesar 0,57 dan Pielou sebesar 0,32. Kata kunci : TWA Suranadi, Lumut Kerak, Identifikasi, Nilai Keanekaragaman Abstract Lichen is a symbiosis between fungi and algae or cyanobacterium, which are useful as bioresource, bioindicator and ecosystem studies. In this research, several aspects of lichen will be examined including species composition along with the number of individuals of each species and the value of lichen diversity. This research is descriptive explorative which was conducted in October-December 2016. -
Lichen 101: What an Arborist Needs to Know About Lichen
Lichen 101: What An Arborist Needs To Know About Lichen Joe Murray Consulting Arborist/Educator Williamsville, Virginia You are here "When we try to pick out anything by itself, we find it hitched to everything else in the Universe." Lynchburg, Virginia South Shields, England Burnsville, Virginia Burnsville, Virginia Burnsville, Virginia Crustose Foliose Fruticose Knockan Crag, Scotland Burnsville, Virginia Tree Lungwort (Lobaria pulmonaria) Burnsville, Virginia Sugar Maple (Acer saccharum) Burnsville, Virginia Burnsville, Virginia Tulip Poplar (Liriodendron tulipifera) Burnsville, Virginia White Oak (Quercus alba) Burnsville, Virginia Pitch Pine (Pinus rigida) Burnsville, Virginia Burnsville, Virginia Internal Age & Composition & Growth of Trunk State of Tree Quality of Soil Air Pollution Moisture Regime (Acid Precipitation) Human Climate (Arson, Vandalism) Exposure Fire, Snow, Frost (Sunlight) Disease Exposure (Wind) Local Environment Elevation (forest or field) Influence from Animals & Microflora Moss Lichens Fungi Algae Tree Architecture (Crown Shape) Burnsville, Virginia Tree Architecture (Branch Orientation) Norway Spruce (Picea abies) Pitch Pine (Pinus rigida) Burnsville, Virginia Tree Architecture (Branch Orientation) Norway Spruce (Picea abies) Pitch Pine (Pinus rigida) Stemflow Burnsville, Virginia Burnsville, Virginia http://385867928462337283.weebly.com/precambrian.html http://dapa.ciat.cgiar.org/carbon-sequestration-one-true-green-revolution/ http://www.anselm.edu/homepage/jpitocch/genbi101/ecology2communities.html Knockan -
Neoproterozoic Origin and Multiple Transitions to Macroscopic Growth in Green Seaweeds
bioRxiv preprint doi: https://doi.org/10.1101/668475; this version posted June 12, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Neoproterozoic origin and multiple transitions to macroscopic growth in green seaweeds Andrea Del Cortonaa,b,c,d,1, Christopher J. Jacksone, François Bucchinib,c, Michiel Van Belb,c, Sofie D’hondta, Pavel Škaloudf, Charles F. Delwicheg, Andrew H. Knollh, John A. Raveni,j,k, Heroen Verbruggene, Klaas Vandepoeleb,c,d,1,2, Olivier De Clercka,1,2 Frederik Leliaerta,l,1,2 aDepartment of Biology, Phycology Research Group, Ghent University, Krijgslaan 281, 9000 Ghent, Belgium bDepartment of Plant Biotechnology and Bioinformatics, Ghent University, Technologiepark 71, 9052 Zwijnaarde, Belgium cVIB Center for Plant Systems Biology, Technologiepark 71, 9052 Zwijnaarde, Belgium dBioinformatics Institute Ghent, Ghent University, Technologiepark 71, 9052 Zwijnaarde, Belgium eSchool of Biosciences, University of Melbourne, Melbourne, Victoria, Australia fDepartment of Botany, Faculty of Science, Charles University, Benátská 2, CZ-12800 Prague 2, Czech Republic gDepartment of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD 20742, USA hDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, Massachusetts, 02138, USA. iDivision of Plant Sciences, University of Dundee at the James Hutton Institute, Dundee, DD2 5DA, UK jSchool of Biological Sciences, University of Western Australia (M048), 35 Stirling Highway, WA 6009, Australia kClimate Change Cluster, University of Technology, Ultimo, NSW 2006, Australia lMeise Botanic Garden, Nieuwelaan 38, 1860 Meise, Belgium 1To whom correspondence may be addressed. Email [email protected], [email protected], [email protected] or [email protected]. -
British Lichen Society Bulletin No
1 BRITISH LICHEN SOCIETY OFFICERS AND CONTACTS 2010 PRESIDENT S.D. Ward, 14 Green Road, Ballyvaghan, Co. Clare, Ireland, email [email protected]. VICE-PRESIDENT B.P. Hilton, Beauregard, 5 Alscott Gardens, Alverdiscott, Barnstaple, Devon EX31 3QJ; e-mail [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: position currently vacant. -
Comparative Analysis of Growth and Carotenoid Accumulation of Trentepohlia Arborum in Aerial, Subaerial, and Aquatic Cultivation
J Appl Phycol DOI 10.1007/s10811-014-0436-x Comparative analysis of growth and carotenoid accumulation of Trentepohlia arborum in aerial, subaerial, and aquatic cultivation Lin Chen & Lanlan Zhang & Wei Zhang & Tianzhong Liu Received: 17 June 2014 /Revised and accepted: 30 September 2014 # Springer Science+Business Media Dordrecht 2014 Abstract The aerial filamentous microalga, Trentepohlia Introduction arborum (Chlorophyta), was cultured in three habitats - an aerial, a subaerial and an aquatic one - using different types of The algal genus Trentepohlia is widespread in different loca- bioreactors. The growth, carotenoid productivity, and morpho- tions such as tropical, subtropical, and temperate regions, even logic differences of T. arborum in different habitats were inves- in frigid zones (Allali et al. 2013;Nashetal.1987; Jorgensen tigated. The maximum specific growth rate (μ)ofthealga and Tonsberg 1988; Liu et al. 2012). The colonies of obtained in the logarithmic phase in the subaerial habitat was Trentepohlia generally grow on the surface of rocks, soil, 0.034 h−1. HPLC analysis also demonstrated that T. arborum walls, or tree trunks, to form a spectacular orange or red accumulated a high content of carotenoids. Zeaxanthin was the “carpet” named “Red stone” (Liu et al. 2012), because it is primary carotenoid in subaerial culture, while β,β-carotene was rich in carotenoid content, especially β-carotene (Kjosen et al. dominant in aerial culture. The maximum carotenoid produc- 1972; Czeczuga and Maximov 1996; Abe et al. 1998; tivity, 67.7 mg m−2 day−1, was reached when T. arborum was Mukherjee et al. 2010). Moreover, some carotenoids, unique cultured in the subaerial habitat under nitrogen depletion using to this group, have been found in Trentepohlia gobii a novel attached cultivation bioreactor. -
Angiactis, a New Crustose Lichen Genus in the Roccellaceae, with Species from Bermuda, the Galápagos Islands and Australia
Angiactis, a new crustose lichen genus in the Roccellaceae, with species from Bermuda, the Gala´pagos Islands and Australia ANDRE´ APTROOT ABL Herbarium, Gerrit van der Veenstraat 107, NL-3762 XK Soest, The Netherlands e-mail: [email protected] LAURENS B. SPARRIUS BIO.DIV, Vrijheidslaan 27, NL-2806 KE Gouda, The Netherlands e-mail: [email protected] SCOTT LAGRECA Department of Botany, the Natural History Museum, Cromwell Road, London SW7 5BD, United Kingdom e-mail: [email protected] FRANK BUNGARTZ Botany Department, Charles Darwin Research Station, Isla Santa Cruz, Gala´pagos; Postal Address: Charles Darwin Foundation, Av. 6 de Diciembre N 36-109 y Pasaje California, Post Box 17-01-3891, Quito, Ecuador e-mail: [email protected] ABSTRACT. The new genus Angiactis Aptroot & Sparrius is described, with three species, A. bermudensis LaGreca sp. nov. from Bermuda, A. littoralis (Kantvilas) Aptroot & Sparrius comb. nov. from Australia and A. spinicola Aptroot & Sparrius sp. nov. from the Gala´pagos. The new genus differs from Lecanographa in the presence of a thalline exciple, and from Llimonaea in the non-corticate thallus and presence of a thalline exciple. KEYWORDS. Angiactis, Arthoniales, Lecanographa, Llimonaea. ¤¤¤ During the last decade, a number of old crustose example, Egea and Torrente (1994) split Lecanactis Roccellaceae genera have been revised by various s.l. into several taxa, based on apothecium shape and workers, revealing new characters. As part of this pigments, and gave more attention to ascospore and process, several larger genera in the family have been ascus characters. As part of this work, related genera reduced in size, such as Enterographa (Sparrius 2004) such as Llimonaea (Torrente & Egea 1991) were and Plectocarpon (Ertz et al.