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The Lichens' Microbiota, Still a Mystery?
fmicb-12-623839 March 24, 2021 Time: 15:25 # 1 REVIEW published: 30 March 2021 doi: 10.3389/fmicb.2021.623839 The Lichens’ Microbiota, Still a Mystery? Maria Grimm1*, Martin Grube2, Ulf Schiefelbein3, Daniela Zühlke1, Jörg Bernhardt1 and Katharina Riedel1 1 Institute of Microbiology, University Greifswald, Greifswald, Germany, 2 Institute of Plant Sciences, Karl-Franzens-University Graz, Graz, Austria, 3 Botanical Garden, University of Rostock, Rostock, Germany Lichens represent self-supporting symbioses, which occur in a wide range of terrestrial habitats and which contribute significantly to mineral cycling and energy flow at a global scale. Lichens usually grow much slower than higher plants. Nevertheless, lichens can contribute substantially to biomass production. This review focuses on the lichen symbiosis in general and especially on the model species Lobaria pulmonaria L. Hoffm., which is a large foliose lichen that occurs worldwide on tree trunks in undisturbed forests with long ecological continuity. In comparison to many other lichens, L. pulmonaria is less tolerant to desiccation and highly sensitive to air pollution. The name- giving mycobiont (belonging to the Ascomycota), provides a protective layer covering a layer of the green-algal photobiont (Dictyochloropsis reticulata) and interspersed cyanobacterial cell clusters (Nostoc spec.). Recently performed metaproteome analyses Edited by: confirm the partition of functions in lichen partnerships. The ample functional diversity Nathalie Connil, Université de Rouen, France of the mycobiont contrasts the predominant function of the photobiont in production Reviewed by: (and secretion) of energy-rich carbohydrates, and the cyanobiont’s contribution by Dirk Benndorf, nitrogen fixation. In addition, high throughput and state-of-the-art metagenomics and Otto von Guericke University community fingerprinting, metatranscriptomics, and MS-based metaproteomics identify Magdeburg, Germany Guilherme Lanzi Sassaki, the bacterial community present on L. -
Diversity and Distribution of Lichen-Associated Fungi in the Ny-Ålesund Region (Svalbard, High Arctic) As Revealed by 454 Pyrosequencing
www.nature.com/scientificreports OPEN Diversity and distribution of lichen- associated fungi in the Ny-Ålesund Region (Svalbard, High Arctic) as Received: 31 March 2015 Accepted: 20 August 2015 revealed by 454 pyrosequencing Published: 14 October 2015 Tao Zhang1, Xin-Li Wei2, Yu-Qin Zhang1, Hong-Yu Liu1 & Li-Yan Yu1 This study assessed the diversity and distribution of fungal communities associated with seven lichen species in the Ny-Ålesund Region (Svalbard, High Arctic) using Roche 454 pyrosequencing with fungal-specific primers targeting the internal transcribed spacer (ITS) region of the ribosomal rRNA gene. Lichen-associated fungal communities showed high diversity, with a total of 42,259 reads belonging to 370 operational taxonomic units (OTUs) being found. Of these OTUs, 294 belonged to Ascomycota, 54 to Basidiomycota, 2 to Zygomycota, and 20 to unknown fungi. Leotiomycetes, Dothideomycetes, and Eurotiomycetes were the major classes, whereas the dominant orders were Helotiales, Capnodiales, and Chaetothyriales. Interestingly, most fungal OTUs were closely related to fungi from various habitats (e.g., soil, rock, plant tissues) in the Arctic, Antarctic and alpine regions, which suggests that living in association with lichen thalli may be a transient stage of life cycle for these fungi and that long-distance dispersal may be important to the fungi in the Arctic. In addition, host-related factors shaped the lichen-associated fungal communities in this region. Taken together, these results suggest that lichens thalli act as reservoirs of diverse fungi from various niches, which may improve our understanding of fungal evolution and ecology in the Arctic. The Arctic is one of the most pristine regions of the planet, and its environment exhibits extreme condi- tions (e.g., low temperature, strong winds, permafrost, and long periods of darkness and light) and offers unique opportunities to explore extremophiles. -
St Kilda Lichen Survey April 2014
A REPORT TO NATIONAL TRUST FOR SCOTLAND St Kilda Lichen Survey April 2014 Andy Acton, Brian Coppins, John Douglass & Steve Price Looking down to Village Bay, St. Kilda from Glacan Conachair Andy Acton [email protected] Brian Coppins [email protected] St. Kilda Lichen Survey Andy Acton, Brian Coppins, John Douglass, Steve Price Table of Contents 1 INTRODUCTION ............................................................................................................ 3 1.1 Background............................................................................................................. 3 1.2 Study areas............................................................................................................. 4 2 METHODOLOGY ........................................................................................................... 6 2.1 Field survey ............................................................................................................ 6 2.2 Data collation, laboratory work ................................................................................ 6 2.3 Ecological importance ............................................................................................. 7 2.4 Constraints ............................................................................................................. 7 3 RESULTS SUMMARY ................................................................................................... 8 4 MARITIME GRASSLAND (INCLUDING SWARDS DOMINATED BY PLANTAGO MARITIMA AND ARMERIA -
Lichenicolous Biota (Nos 201–230)
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Fritschiana Jahr/Year: 2015 Band/Volume: 80 Autor(en)/Author(s): Hafellner Josef Artikel/Article: Lichenicolous Biota (Nos 201-230) 21-41 - 21 - Lichenicolous Biota (Nos 201–230) Josef HAFELLNER* HAFELLNER Josef 2015: Lichenicolous Biota (Nos 201–230). – Frit- schiana (Graz) 80: 21–41. - ISSN 1024-0306. Abstract: The 9th fascicle (30 numbers) of the exsiccata 'Lichenicolous Biota' is published. The issue contains ma- terial of 20 non-lichenized fungal taxa (14 teleomorphs of ascomycetes, 4 anamorphic states of ascomycetes, 2 an- amorphic states of basidiomycetes) and 9 lichenized as- comycetes, including paratype material of Dimelaena li- chenicola K.Knudsen et al. (no 223), Miriquidica invadens Hafellner et al. (no 226, 227), and Stigmidium xantho- parmeliarum Hafellner (no 210). Furthermore, collections of the type species of the following genera are distributed: Illosporiopsis (I. christiansenii), Illosporium (I. carneum), Marchandiomyces (M. corallinus), Marchandiobasidium (M. aurantiacum, sub Erythricium aurantiacum), Micro- calicium (M. disseminatum), Nigropuncta (N. rugulosa), Paralecanographa (P. grumulosa), Phaeopyxis (P. punc- tum), Placocarpus (P. schaereri), Rhagadostoma (R. li- chenicola), and Stigmidium (S. schaereri). *Institut für Pflanzenwissenschaften, NAWI Graz, Karl-Franzens-Universität, Holteigasse 6, 8010 Graz, AUSTRIA e-mail: [email protected] Introduction The exsiccata 'Lichenicolous Biota' is continued with fascicle 9, containing 30 numbers. The exsiccata covers all lichenicolous biota, i.e., it is open not only to non- lichenized and lichenized fungi, but also to myxomycetes, bacteria, and even animals, whenever they cause a characteristic symptom on their host (e.g. discoloration or galls). -
Molecular Phylogenetic Study at the Generic Boundary Between the Lichen-Forming Fungi Caloplaca and Xanthoria (Ascomycota, Teloschistaceae)
Mycol. Res. 107 (11): 1266–1276 (November 2003). f The British Mycological Society 1266 DOI: 10.1017/S0953756203008529 Printed in the United Kingdom. Molecular phylogenetic study at the generic boundary between the lichen-forming fungi Caloplaca and Xanthoria (Ascomycota, Teloschistaceae) Ulrik SØCHTING1 and Franc¸ ois LUTZONI2 1 Department of Mycology, Botanical Institute, University of Copenhagen, O. Farimagsgade 2D, DK-1353 Copenhagen K, Denmark. 2 Department of Biology, Duke University, Durham, NC 27708-0338, USA. E-mail : [email protected] Received 5 December 2001; accepted 5 August 2003. A molecular phylogenetic analysis of rDNA was performed for seven Caloplaca, seven Xanthoria, one Fulgensia and five outgroup species. Phylogenetic hypotheses are constructed based on nuclear small and large subunit rDNA, separately and in combination. Three strongly supported major monophyletic groups were revealed within the Teloschistaceae. One group represents the Xanthoria fallax-group. The second group includes three subgroups: (1) X. parietina and X. elegans; (2) basal placodioid Caloplaca species followed by speciations leading to X. polycarpa and X. candelaria; and (3) a mixture of placodioid and endolithic Caloplaca species. The third main monophyletic group represents a heterogeneous assemblage of Caloplaca and Fulgensia species with a drastically different metabolite content. We report here that the two genera Caloplaca and Xanthoria, as well as the subgenus Gasparrinia, are all polyphyletic. The taxonomic significance of thallus morphology in Teloschistaceae and the current delimitation of the genus Xanthoria is discussed in light of these results. INTRODUCTION Taxonomy of Teloschistaceae and its genera The Teloschistaceae is a well-delimited family of Hawksworth & Eriksson (1986) assigned the Teloschis- lichenized fungi. -
Die Gattung Aspicilia, Ihre Ableitungen Nebst
Acta Botánica Malacitana, 16(1): 133-140 Malaga, 1991 DIE GAUG ASPICILIA, IE AEIUGE ES EMEKUGE OE CYOECAOIE ASCOCAOGAISAIO EI AEE GENERA E LECANORALES (ASCOMYCEES ICEISAI Josef HAFELLNER SUMMARY: Some evolutionary lines are shown within Aspicilia coll, and the taxonomical and nomenclatural consequences for species commonly classified in Sphaerothallia Nees are discussed. The generic rank (Lobothallia (Clauzade & Roux) Hafellner) is proposed for the Aspicilia radiosa group and the following new combinations are introduced: Lobothallia alphoplaca (Wahlenb. in Ach.)Haf., Lobothallia melanaspis (Ach.)Haf., Lobothallia praeradiosa (Nyl.)Haf. and Lobothallia radiosa (Hoffm.)Haf. Key words: Lichenized Ascomycetes, Aspicilia, Lobothallia, taxonomy. ZUSAMMENFASSUNG: Innerhalb der Gattung Aspicilia coll. werden einige Evolutionslinien aufgezeigt und taxonomische wie nomenklatorische Konsequenzen für gewtihnlich als Sphaerothallia Nees bezeichnete Arten werden diskutiert. Lobothallia (Clauzade & Roux) Hafellner wird in den Gattungsrang erhoben und folgende neue Kombinationen werden vorgeschlagen: Lobythallia alphoplaca (Wahlenb. in Ach) Haf., Lobothallia melanaspis (Ach) Haf., Lobothallia praeradiosa (NYL.) Haf. und Lobothallia radiosa (Hoffm.)Haf. Schltisselwórter: Licheniscerte Ascomyceten, Aspiclia, Lobothallia, Taxonomie. EINLEITUNG Der schon von Massalongo (1852) beschriebenen Gattung Aspicilia war emn wechselvolles Schicksal beschieden. Ober lange Zeit in Lecanora eingeschlossen und oft in dieser als Subgenus bewertet (z.B. Magnusson 1939, Poelt 1958, Eigler 1969), hat sich erst in jtingerer Zeit die Erkenntnis allgemein durchgesetzt, daB Aspicilia mit Lecanora nicht ndher verwandt ist (Poelt 1974, Roux 1977, Hawksworth & al. 1980, Santesson 1984, Clauzade & Roux 1984, 1987, Hafellner 1984, Esnault 1985), obwohl einige Autoren schon früh die Selbstdndigkeit betont hatten (z.B. Kürber 1855, Hue 1910, Choisy 1929). Poelt (1974) hat sogar die neue Familie Aspiciliaceae vorgeschlagen, urn die taxonomische Distanz zwischen Aspicilia und Lecanora augenfdllig zu machen. -
Domenico Puntillo & Sonia Ravera Naetrocymbe Mori
Fl. Medit. 23: 5-9 doi: 10.7320/FlMedit23.005 Version of Record published online on 30 December 2013 Domenico Puntillo & Sonia Ravera Naetrocymbe mori-albae, a new species from Calabria (Southern Italy) Abstract Puntillo, D. & Ravera S.: Naetrocymbe mori-albae, a new species from Calabria (Southern Italy). — Fl. Medit. 23: 5-9. 2013. — ISSN: 1120-4052 printed, 2240-4538 online. The new taxon belongs to the group Arthopyrenia rhyponta-A. punctiformis, recently trans- ferred to the problematic genus Naetrocymbe Korb. (Naetrocymbaceae Höhn. ex R.C. Harris), as it is a non or weakly lichenized group. This species is characterized by tadpole-shaped 1-sep- tate ascospores with a conical lower cell and perithecia which are 4-8 linearly arranged. Key words: Naetrocymbe, Lichenes, Italy. Introduction Naetrocymbe is a genus of pyrenocarpous ascomycetes belonging to the family Naetrocymbaceae establish by Harris (1995). This family includes species usually not lichen-forming and characterized by short-celled paraphyses with refractive bodies near the septa, obpyriform asci with a distinctive apical region lacking a nasse and short rod- shaped microconidia. It has a mainly temperate/boreal distribution. Because of some Naetrocymbe species can be lichenized (Keissler 1938; Knudsen & Lendemer 2009; Roux 2009), Aptroot (1998, 2002), Coppins (2002) and Coppins & Orange (2009) consider unnecessary a separation between Naetrocymbe and Arthopyrenia. They disagree with Harris (1973, 1975, 1995), Tucker & Harris (1980) and Coppins (1988), about the impor- tance of the hamathecial tissues as valuable character. In Aptroot’s opinion, the cosmopol- itan genus Arthopyrenia s.l. should be considered in its original wide concept: character- ized by branched pseudoparaphyses, which may disappear, and sole-shaped ascospores. -
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. -
1307 Fungi Representing 1139 Infrageneric Taxa, 317 Genera and 66 Families ⇑ Jolanta Miadlikowska A, , Frank Kauff B,1, Filip Högnabba C, Jeffrey C
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, Soili Stenroos c,10 a Department of Biology, Duke University, Durham, NC 27708-0338, USA b FB Biologie, Molecular Phylogenetics, 13/276, TU Kaiserslautern, Postfach 3049, 67653 Kaiserslautern, Germany c Botanical Museum, Finnish Museum of Natural History, FI-00014 University of Helsinki, Finland d Department of Ecology and Evolutionary Biology, Yale University, 358 ESC, 21 Sachem Street, New Haven, CT 06511, USA e Institut für Botanik, Karl-Franzens-Universität, Holteigasse 6, A-8010 Graz, Austria f Department of Plant Taxonomy and Nature Conservation, University of Gdan´sk, ul. Wita Stwosza 59, 80-308 Gdan´sk, Poland g Science and Education, The Field Museum, 1400 S. -
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. -
Lichen Functional Trait Variation Along an East-West Climatic Gradient in Oregon and Among Habitats in Katmai National Park, Alaska
AN ABSTRACT OF THE THESIS OF Kaleigh Spickerman for the degree of Master of Science in Botany and Plant Pathology presented on June 11, 2015 Title: Lichen Functional Trait Variation Along an East-West Climatic Gradient in Oregon and Among Habitats in Katmai National Park, Alaska Abstract approved: ______________________________________________________ Bruce McCune Functional traits of vascular plants have been an important component of ecological studies for a number of years; however, in more recent times vascular plant ecologists have begun to formalize a set of key traits and universal system of trait measurement. Many recent studies hypothesize global generality of trait patterns, which would allow for comparison among ecosystems and biomes and provide a foundation for general rules and theories, the so-called “Holy Grail” of ecology. However, the majority of these studies focus on functional trait patterns of vascular plants, with a minority examining the patterns of cryptograms such as lichens. Lichens are an important component of many ecosystems due to their contributions to biodiversity and their key ecosystem services, such as contributions to mineral and hydrological cycles and ecosystem food webs. Lichens are also of special interest because of their reliance on atmospheric deposition for nutrients and water, which makes them particularly sensitive to air pollution. Therefore, they are often used as bioindicators of air pollution, climate change, and general ecosystem health. This thesis examines the functional trait patterns of lichens in two contrasting regions with fundamentally different kinds of data. To better understand the patterns of lichen functional traits, we examined reproductive, morphological, and chemical trait variation along precipitation and temperature gradients in Oregon. -
The Fungi of Slapton Ley National Nature Reserve and Environs
THE FUNGI OF SLAPTON LEY NATIONAL NATURE RESERVE AND ENVIRONS APRIL 2019 Image © Visit South Devon ASCOMYCOTA Order Family Name Abrothallales Abrothallaceae Abrothallus microspermus CY (IMI 164972 p.p., 296950), DM (IMI 279667, 279668, 362458), N4 (IMI 251260), Wood (IMI 400386), on thalli of Parmelia caperata and P. perlata. Mainly as the anamorph <it Abrothallus parmeliarum C, CY (IMI 164972), DM (IMI 159809, 159865), F1 (IMI 159892), 2, G2, H, I1 (IMI 188770), J2, N4 (IMI 166730), SV, on thalli of Parmelia carporrhizans, P Abrothallus parmotrematis DM, on Parmelia perlata, 1990, D.L. Hawksworth (IMI 400397, as Vouauxiomyces sp.) Abrothallus suecicus DM (IMI 194098); on apothecia of Ramalina fustigiata with st. conid. Phoma ranalinae Nordin; rare. (L2) Abrothallus usneae (as A. parmeliarum p.p.; L2) Acarosporales Acarosporaceae Acarospora fuscata H, on siliceous slabs (L1); CH, 1996, T. Chester. Polysporina simplex CH, 1996, T. Chester. Sarcogyne regularis CH, 1996, T. Chester; N4, on concrete posts; very rare (L1). Trimmatothelopsis B (IMI 152818), on granite memorial (L1) [EXTINCT] smaragdula Acrospermales Acrospermaceae Acrospermum compressum DM (IMI 194111), I1, S (IMI 18286a), on dead Urtica stems (L2); CY, on Urtica dioica stem, 1995, JLT. Acrospermum graminum I1, on Phragmites debris, 1990, M. Marsden (K). Amphisphaeriales Amphisphaeriaceae Beltraniella pirozynskii D1 (IMI 362071a), on Quercus ilex. Ceratosporium fuscescens I1 (IMI 188771c); J1 (IMI 362085), on dead Ulex stems. (L2) Ceriophora palustris F2 (IMI 186857); on dead Carex puniculata leaves. (L2) Lepteutypa cupressi SV (IMI 184280); on dying Thuja leaves. (L2) Monographella cucumerina (IMI 362759), on Myriophyllum spicatum; DM (IMI 192452); isol. ex vole dung. (L2); (IMI 360147, 360148, 361543, 361544, 361546).