An Introduction to Lichens
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A Study of the Pruinose Species of Hypogymnia (Parmeliaceae, Ascomycota) from China
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/259425488 A study of the pruinose species of Hypogymnia (Parmeliaceae, Ascomycota) from China Article in The Lichenologist · November 2012 DOI: 10.1017/S0024282912000473 CITATIONS READS 3 134 2 authors, including: Xinli Wei Institute of Microbiology Chinese Academy of Sciences 65 PUBLICATIONS 355 CITATIONS SEE PROFILE Some of the authors of this publication are also working on these related projects: Lichen species composition and distribution in China View project Discovering the possibility of life on Mars View project All content following this page was uploaded by Xinli Wei on 09 June 2015. The user has requested enhancement of the downloaded file. The Lichenologist 44(6): 783–793 (2012) 6 British Lichen Society, 2012 doi:10.1017/S0024282912000473 A study of the pruinose species of Hypogymnia (Parmeliaceae, Ascomycota) from China Xin-Li WEI and Jiang-Chun WEI Abstract: Six pruinose species of Hypogymnia are reported in this paper, including one new species Hypogymnia pruinoidea. The type of Hypogymnia pseudopruinosa was found to be a mixture with H. laccata. Hypogymnia pseudopruinosa is therefore typified with a lectotype, and the description of H. pseudopruinosa is revised. Distributions of the six pruinose species are given and discussed. Com- ments on differences and similarities between pruinose species of Hypogymnia are made. Diagnostic characters of each species, and a key to the pruinose species of Hypogymnia in China, are also provided. Key words: H. pruinoidea, H. pseudopruinosa, lichen substances, pruina Accepted for publication 6 June 2012 Introduction Materials and Methods Although over 100 species of Hypogymnia Specimens treated here are preserved in the Lichen (Nyl.) Nyl. -
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. -
Monitoring Air Quality in Class I Wilderness Areas of the Northeastern United States Using Lichens and Bryophytes Alison C
United States Department of Agriculture Monitoring Air Quality in Class I Wilderness Areas of the Northeastern United States Using Lichens and Bryophytes Alison C. Dibble, James W. Hinds, Ralph Perron, Natalie Cleavitt, Richard L. Poirot, and Linda H. Pardo Forest Service Northern Research Station General Technical Report NRS-165 December 2016 1 Abstract To address a need for air quality and lichen monitoring information for the Northeast, we compared bulk chemistry data from 2011-2013 to baseline surveys from 1988 and 1993 in three Class I Wilderness areas of New Hampshire and Vermont. Plots were within the White Mountain National Forest (Presidential Range—Dry River Wilderness and Great Gulf Wilderness, New Hampshire) and the Green Mountain National Forest (Lye Brook Wilderness, Vermont). We sampled epiphyte communities and found 58 macrolichen species and 55 bryophyte species. We also analyzed bulk samples for total N, total S, and 27 additional elements. We detected a decrease in Pb at the level of the National Forest and in a subset of plots. Low lichen richness and poor thallus condition at Lye Brook corresponded to higher N and S levels at these sites. Lichen thallus condition was best where lichen species richness was also high. Highest Hg content, from a limited subset, was on the east slope of Mt. Washington near the head of Great Gulf. Most dominant lichens in good condition were associated with conifer boles or acidic substrates. The status regarding N and S tolerance for many lichens in the northeastern United States is not clear, so the influence of N pollution on community data cannot be fully assessed. -
Assessment of Lichens As Biomonitors of Heavy Metal Pollution in Selected Mining Area, Slovakia Amer H
ISSN-1996-918X Cross Mark Pak. J. Anal. Environ. Chem. Vol. 22, No. 1 (2021) 53 – 59 http://doi.org/10.21743/pjaec/2021.06.07 Assessment of Lichens as Biomonitors of Heavy Metal Pollution in Selected Mining Area, Slovakia Amer H. Tarawneh1, Ivan Salamon2*, Rakan M. Altarawneh3, Jozef Mitra1 and Anastassiya Gadetskaya4 1Tafila Technical University, Department of Chemistry and Chemical Technology, P.O.Box 179, Tafila 66110, Jordan. 2University of Presov, Faculty of Humanities and Natural Science, Department of Ecology, 01, 17th November St., 081 16, Presov, Slovakia. 3Chemistry Department, Faculty of Science, Mutah University, Karak 61710, Jordan. 4School of Chemistry and Chemical Technology, Al-Farabi Kazakh National University, Almaty 050040, Kazakhstan. *Corresponding Author Email: [email protected] Received 07 September 2020, Revised 23 April 2021, Accepted 26 April 2021 -------------------------------------------------------------------------------------------------------------------------------------------- Abstract Lichens have widely been used as bioindicators to reflect the quality of the environment. The present study was conducted to investigate the lichens diversity that grows on the surface of waste heaps from an abandoned old copper mine in Mlynky, Slovakia. In spite of the heavy metal- contaminated environment, we documented twenty species of lichens in the selected site. Taxonomically the most numerous group were represented by Cladonia with seven species, as well other species; namely, Acarospora fuscata, Cetraria islandica, Dermatocarpon miniatum, Hypogymnia physodes, Hypogymnia tubulosa, Lecanora subaurea, Lepraria incana, Physcia aipolia, Porpidia macrocarpa, Pseudevernia furfuracea, Rhizocarpon geographicum and Xanthoria parietina. The content of selected heavy metals (Cu, Fe, and Zn) in the predominant lichens Cetraria islandica, Cladonia digitata, Cladonia pyxidata, Hypogymnia physodes and Pseudevernia furfuracea were analyzed. -
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. -
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 -
The Lichen Genus Hypogymnia in Southwest China Article
Mycosphere 5 (1): 27–76 (2014) ISSN 2077 7019 www.mycosphere.org Article Mycosphere Copyright © 2014 Online Edition Doi 10.5943/mycosphere/5/1/2 The lichen genus Hypogymnia in southwest China McCune B1 and Wang LS2 1 Department of Botany and Plant Pathology, Oregon State University, Corvallis, Oregon 97331-2902 U.S.A. 2 Key Laboratory of Biodiversity and Biogeography, Kunming Institute of Botany, Chinese Academy of Sciences, Heilongtan, Kunming 650204, China McCune B, Wang LS 2014 – The lichen genus Hypogymnia in southwest China. Mycosphere 5(1), 27–76, Doi 10.5943/mycosphere/5/1/2 Abstract A total of 36 species of Hypogymnia are known from southwestern China. This region is a center of biodiversity for the genus. Hypogymnia capitata, H. nitida, H. saxicola, H. pendula, and H. tenuispora are newly described species from Yunnan and Sichuan. Olivetoric acid is new as a major lichen substance in Hypogymnia, occurring only in H. capitata. A key and illustrations are given for the species known from this region, along with five species from adjoining regions that might be confused or have historically been misidentified in this region. Key words – Lecanorales – lichenized ascomycetes – Parmeliaceae – Shaanxi – Sichuan – Tibet – Yunnan – Xizang. Introduction The first major collections of Hypogymnia from southwestern China were by Handel- Mazzetti, from which Zahlbruckner (1930) reported six species now placed in Hypogymnia, and Harry Smith (1921-1934, published piecewise by other authors; Herner 1988). Since the last checklist of lichens in China (Wei 1991), which reported 16 species of Hypogymnia from the southwestern provinces, numerous species of Hypogymnia from southwestern China have been described or revised (Chen 1994, Wei & Bi 1998, McCune & Obermayer 2001, McCune et al. -
Heritage Rank Status Factors
Heritage Rank Status Factors Elcode NLLEC84160 Gname HYPOGYMNIA VITTATA Gcomname Number of Occurrences E = >300 Comments Wide distribution in the northern hemisphere, so probably a large number of occurences. Number of Occurrences with Good Viability F = Very many (>125) occurrences with good viability Comments Population Size F = 10,000-100,000 individuals Comments Range Extent H = > 2,500,000 km2 (greater than 1,000,000 square miles) Comments Known from coastal Alaska, British Columbia (McCune & Geiser 1997) and also reported by Brodo et al. (2001) in Washington and Oregon, the Appalachian Mountains, as well as other parts of Canada and New England. Reported from high montane areas in Germany (Wirth 1995), from Austria (Berger and Priemetzhofer 2000), the Kanin-Pechora subprovince of the Arctic floristic region (rare) (Lavrinenko et al. 2000), the Ukraine. (Kodnratyuk 1992), northernmost Siberia (Zhurbenko and Hansen 1992), Australasia (Elix 1980), and Japan (Kurokawa 1971). A boreal- temperate, slightly oceanic, more-or-less circumpolar species (Krog 1968). Area of Occupancy H = >20,000 km2 (greater than 5,000,000 acres) LH = >200,000 km (greater than 125,000 miles) Comments Long-term Trend in Population Size, Extent of Occurrence, Area of Occupancy, and/or Number or Condition of Occurrences E = Relatively Stable (±25% change) Comments Short-term Trend in Population Size, Extent of Occurrence, Area of Occupancy, and/or Number or Condition of Occurrences E = Stable. Population, range, area occupied, and/or number or condition of occurrences unchanged or remaining within ±10% fluctuation Comments Threats U = Unknown. The available information is not sufficient to assign degree of threat as above. -
Hypogymnia Physodes and Its Genetic Diversity
Ann. Bot. Fennici 48: 473–482 ISSN 0003-3847 (print) ISSN 1797-2442 (online) Helsinki 30 December 2011 © Finnish Zoological and Botanical Publishing Board 2011 Depsides and depsidones in populations of the lichen Hypogymnia physodes and its genetic diversity Katalin Molnár* & Edit Farkas Institute of Ecology and Botany, Hungarian Academy of Sciences, H-2163 Vácrátót, Hungary (*corresponding author’s e-mail: [email protected]) Received 18 Oct. 2010, revised version received 20 Dec. 2010, accepted 22 Dec. 2010 Molnár, K. & Farkas, E. 2011: Depsides and depsidones in populations of the lichen Hypogymnia physodes and its genetic diversity. — Ann. Bot. Fennici 48: 473–482. The aim of this study was to determine the extent and geographical pattern of intraspe- cific chemical and genetic variability of the lichen Hypogymnia physodes by compar- ing populations from different habitats. We analyzed the secondary lichen substances and their relative concentrations using HPTLC and HPLC in samples collected from sites with different environmental conditions. We identified seven lichen substances: the cortical atranorin and chloroatranorin, and the medullary physodalic, physodic, protocetraric, 3-hydroxyphysodic, and 2´-O-methylphysodic acids. The samples were uniform qualitatively, which means that H. physodes has only one chemotype. We detected quantitative chemical differences between the samples without any geo- graphical pattern. We investigated 21 samples in order to study the connection between genotypic diversity of populations and geographical distribution. We determined the sequences of five loci (ITS, nucSSU, nucLSU, mitSSU, EF1α). We found no significant genetic differentiation among populations collected from different areas. Introduction 1989, Pfeiffer & Barclay-Estrup 1992, Bruteig 1993, Werner 1993, Bennett et al. -
A Field Guide to Biological Soil Crusts of Western U.S. Drylands Common Lichens and Bryophytes
A Field Guide to Biological Soil Crusts of Western U.S. Drylands Common Lichens and Bryophytes Roger Rosentreter Matthew Bowker Jayne Belnap Photographs by Stephen Sharnoff Roger Rosentreter, Ph.D. Bureau of Land Management Idaho State Office 1387 S. Vinnell Way Boise, ID 83709 Matthew Bowker, Ph.D. Center for Environmental Science and Education Northern Arizona University Box 5694 Flagstaff, AZ 86011 Jayne Belnap, Ph.D. U.S. Geological Survey Southwest Biological Science Center Canyonlands Research Station 2290 S. West Resource Blvd. Moab, UT 84532 Design and layout by Tina M. Kister, U.S. Geological Survey, Canyonlands Research Station, 2290 S. West Resource Blvd., Moab, UT 84532 All photos, unless otherwise indicated, copyright © 2007 Stephen Sharnoff, Ste- phen Sharnoff Photography, 2709 10th St., Unit E, Berkeley, CA 94710-2608, www.sharnoffphotos.com/. Rosentreter, R., M. Bowker, and J. Belnap. 2007. A Field Guide to Biological Soil Crusts of Western U.S. Drylands. U.S. Government Printing Office, Denver, Colorado. Cover photos: Biological soil crust in Canyonlands National Park, Utah, cour- tesy of the U.S. Geological Survey. 2 Table of Contents Acknowledgements ....................................................................................... 4 How to use this guide .................................................................................... 4 Introduction ................................................................................................... 4 Crust composition ..................................................................................