Lichens—A Potential Source for Nanoparticles Fabrication: a Review on Nanoparticles Biosynthesis and Their Prospective Applications
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Fossil Usnea and Similar Fruticose Lichens from Palaeogene Amber
The Lichenologist (2020), 52, 319–324 doi:10.1017/S0024282920000286 Standard Paper Fossil Usnea and similar fruticose lichens from Palaeogene amber Ulla Kaasalainen1 , Jouko Rikkinen2,3 and Alexander R. Schmidt1 1Department of Geobiology, University of Göttingen, Göttingen, Germany; 2Finnish Museum of Natural History, University of Helsinki, Helsinki, Finland and 3Organismal and Evolutionary Biology Research Programme, Faculty of Biological and Environmental Sciences, University of Helsinki, Helsinki, Finland Abstract Fruticose lichens of the genus Usnea Dill. ex Adans. (Parmeliaceae), generally known as beard lichens, are among the most iconic epiphytic lichens in modern forest ecosystems. Many of the c. 350 currently recognized species are widely distributed and have been used as bioin- dicators in air pollution studies. Here we demonstrate that usneoid lichens were present in the Palaeogene amber forests of Europe. Based on general morphology and annular cortical fragmentation, one fossil from Baltic amber can be assigned to the extant genus Usnea. The unique type of cortical cracking indirectly demonstrates the presence of a central cord that keeps the branch intact even when its cortex is split into vertebrae-like segments. This evolutionary innovation has remained unchanged since the Palaeogene, contributing to the considerable ecological flexibility that allows Usnea species to flourish in a wide variety of ecosystems and climate regimes. The fossil sets the minimum age for Usnea to 34 million years (late Eocene). While the other similar fossils from Baltic and Bitterfeld ambers cannot be definitely assigned to the same genus, they underline the diversity of pendant lichens in Palaeogene amber forests. Key words: Ascomycota, Baltic amber, Bitterfeld amber, lichen fossils (Accepted 16 April 2020) Introduction 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. -
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 -
Mycobiology Research Article
Mycobiology Research Article Lichen Mycota in South Korea: The Genus Usnea 1 1 1 1 2 1, Udeni Jayalal , Santosh Joshi , Soon-Ok Oh , Young Jin Koh , Florin Criçs an and Jae-Seoun Hur * 1 Korean Lichen Research Institute, Sunchon National University, Suncheon 540-742, Korea 2 Faculty of Biology and Geology, Babeçs -Bolyai University, Cluj-Napoca, 400015, Romania Abstract Usnea Adans. is a somewhat rare lichen in South Korea, and, in nearly two decades, no detailed taxonomic or revisionary study has been conducted. This study was based on the specimens deposited in the lichen herbarium at the Korean Lichen Research Institute, and the samples were identified using information obtained from recent literature. In this study, a total of eight species of Usnea, including one new record, Usnea hakonensis Asahina, are documented. Detailed descriptions of each species with their morphological, anatomical, and chemical characteristics are provided. A key to all known Usnea species in South Korea is also presented. Keywords Key, New record, Parmeliaceae, South Korea, Usnea The lichen genus Usnea Adans. belongs to the family [6] proposed another subgenus Dolichousnea (Y. Ohmura) Parmeliaceae [1] (Lecanorales, Ascomycota), with ca. 300 Articus from the subgenus Usnea. The subgenus Eumitria species, and shows a world-wide distribution [2, 3]. Due to (Stirt.) Zahlbr. and sections Usnea Dill. ex Adans. and a fruticose habit and a beard like appearance, it is easily Ceratinae (Motyka) Y. Ohmura were segregated from the recognized, but difficult to identify up to species level due subgenus Usnea based on the molecular analysis reported to the presence of varying characteristics [4, 5]. -
A Multigene Phylogenetic Synthesis for the Class Lecanoromycetes (Ascomycota): 1307 Fungi Representing 1139 Infrageneric Taxa, 317 Genera and 66 Families
A multigene phylogenetic synthesis for the class Lecanoromycetes (Ascomycota): 1307 fungi representing 1139 infrageneric taxa, 317 genera and 66 families Miadlikowska, J., Kauff, F., Högnabba, F., Oliver, J. C., Molnár, K., Fraker, E., ... & Stenroos, S. (2014). A multigene phylogenetic synthesis for the class Lecanoromycetes (Ascomycota): 1307 fungi representing 1139 infrageneric taxa, 317 genera and 66 families. Molecular Phylogenetics and Evolution, 79, 132-168. doi:10.1016/j.ympev.2014.04.003 10.1016/j.ympev.2014.04.003 Elsevier Version of Record http://cdss.library.oregonstate.edu/sa-termsofuse Molecular Phylogenetics and Evolution 79 (2014) 132–168 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev A multigene phylogenetic synthesis for the class Lecanoromycetes (Ascomycota): 1307 fungi representing 1139 infrageneric taxa, 317 genera and 66 families ⇑ Jolanta Miadlikowska a, , Frank Kauff b,1, Filip Högnabba c, Jeffrey C. Oliver d,2, Katalin Molnár a,3, Emily Fraker a,4, Ester Gaya a,5, Josef Hafellner e, Valérie Hofstetter a,6, Cécile Gueidan a,7, Mónica A.G. Otálora a,8, Brendan Hodkinson a,9, Martin Kukwa f, Robert Lücking g, Curtis Björk h, Harrie J.M. Sipman i, Ana Rosa Burgaz j, Arne Thell k, Alfredo Passo l, Leena Myllys c, Trevor Goward h, Samantha Fernández-Brime m, Geir Hestmark n, James Lendemer o, H. Thorsten Lumbsch g, Michaela Schmull p, Conrad L. Schoch q, Emmanuël Sérusiaux r, David R. Maddison s, A. Elizabeth Arnold t, François Lutzoni a,10, -
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 .................................................................................. -
Learn About Lichen Students Will Learn How to Identify 3 Forms of Lichen
Learn about Lichen Students will learn how to identify 3 forms of lichen. Magnifying glass, clipboard with lichen sheet (page 3) and pencil. Grades: 5-7 30-60 minutes Activity sheet included Introduction Lichen is composed of 2 or more organisms: an algae, cyanobacteria and a fungus living together in a symbiotic mutual partnership (see page 2 for a glossary of all bolded words). Lichen covers 6% of our planet with over 17,000 different species of lichen worldwide. Approximately 1,100 species of lichen are found in British Columbia. Lichen can provide food and habitat for many animals and can help break down rocks to become soil. The fungus provides physical structure and water: the algae and cyanobacteria, using photosynthesis, produce food. Lichen is an excellent indicator of air quality, making it a bioindicator. These hearty pioneer species can be found on every continent on earth. Have you noticed any lichen in your favourite spot in nature? Directions • With your clipboard, pencil, lichen sheet and magnifying glass, head outside to your favourite place in nature. • Look for the three basic forms of lichen: Fruticose (shrubby and branch-like) Crustose (flat and crusty/dusty) and Foliose (leaf-like and has 2 sides). Fruticose Crustose Foliose • Note all the different colours, textures and forms you find on your sheet and try to draw the different forms of lichen you find. So what about moss? Lichen and moss are often mistaken for one another. While certain types of lichen might resemble moss, they are very different. Mosses are defined as simple plants with the most basic of root structures, leaves, and stems. -
Mosses and Lichens
Chapter 9 Plants That Aren’t “Plants”: Mosses and Lichens Clayton Newberry Department of Biological Sciences 4505 Maryland Parkway Box 454004 Las Vegas, NV 89154-4004 [email protected] Clayton Newberry is a graduate student at University of Nevada at Las Vegas. He received his B.S. in general botany from Brigham Young University and his M.S. in lichenology from Brigham Young University. He is currently working on his Ph.D. at University of Nevada at Las Vegas. His interests include bryophyte systematics and bryophyte floristics in western North America. Reprinted From: Newberry, C. 2004. Plants that aren’t “plants”: Mosses and lichens. Pages 179-197, in th Tested studies for laboratory teaching, Volume 25 (M. A. O’Donnell, Editor). Proceedings of the 25 Workshop/Conference of the Association for Biology Laboratory Education (ABLE), 414 pages. - Copyright policy: http://www.zoo.utoronto.ca/able/volumes/copyright.htm Although the laboratory exercises in ABLE proceedings volumes have been tested and due consideration has been given to safety, individuals performing these exercises must assume all responsibility for risk. The Association for Biology Laboratory Education (ABLE) disclaims any liability with regards to safety in connection with the use of the exercises in its proceedings volumes. © 2004 Clayton Newberry Association for Biology Laboratory Education (ABLE) ~ http://www.zoo.utoronto.ca/able 179 180 Mosses and lichens Contents Introduction....................................................................................................................180 -
Lichen-Like Association of Chlamydomonas Reinhardtii and Aspergillus Nidulans Protects Algal Cells from Bacteria
The ISME Journal (2020) 14:2794–2805 https://doi.org/10.1038/s41396-020-0731-2 ARTICLE Lichen-like association of Chlamydomonas reinhardtii and Aspergillus nidulans protects algal cells from bacteria 1,2 3,5 1,2 1,2,6 3 Mario K. C. Krespach ● María García-Altares ● Michal Flak ● Hanno Schoeler ● Kirstin Scherlach ● 1,7 1,2 1 1 2,3 4 Tina Netzker ● Anica Schmalzl ● Derek J. Mattern ● Volker Schroeckh ● Anna Komor ● Maria Mittag ● 2,3 1,2 Christian Hertweck ● Axel A. Brakhage Received: 8 August 2019 / Revised: 15 July 2020 / Accepted: 23 July 2020 / Published online: 4 August 2020 © The Author(s) 2020. This article is published with open access Abstract Organismal interactions within microbial consortia and their responses to harmful intruders remain largely understudied. An important step toward the goal of understanding functional ecological interactions and their evolutionary selection is the study of increasingly complex microbial interaction systems. Here, we discovered a tripartite biosystem consisting of the fungus Aspergillus nidulans, the unicellular green alga Chlamydomonas reinhardtii, and the algicidal bacterium Streptomyces iranensis. Genetic analyses and MALDI-IMS demonstrate that the bacterium secretes the algicidal compound azalomycin F 1234567890();,: 1234567890();,: upon contact with C. reinhardtii. In co-culture, A. nidulans attracts the motile alga C. reinhardtii, which becomes embedded and surrounded by fungal mycelium and is shielded from the algicide. The filamentous fungus Sordaria macrospora was susceptible to azalomycin F and failed to protect C. reinhardtii despite chemotactically attracting the alga. Because S. macrospora was susceptible to azalomycin F, this data imply that for protection the fungus needs to be resistant.