Compiled Key to Xanthoparmelia in Southern Africa
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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. -
H. Thorsten Lumbsch VP, Science & Education the Field Museum 1400
H. Thorsten Lumbsch VP, Science & Education The Field Museum 1400 S. Lake Shore Drive Chicago, Illinois 60605 USA Tel: 1-312-665-7881 E-mail: [email protected] Research interests Evolution and Systematics of Fungi Biogeography and Diversification Rates of Fungi Species delimitation Diversity of lichen-forming fungi Professional Experience Since 2017 Vice President, Science & Education, The Field Museum, Chicago. USA 2014-2017 Director, Integrative Research Center, Science & Education, The Field Museum, Chicago, USA. Since 2014 Curator, Integrative Research Center, Science & Education, The Field Museum, Chicago, USA. 2013-2014 Associate Director, Integrative Research Center, Science & Education, The Field Museum, Chicago, USA. 2009-2013 Chair, Dept. of Botany, The Field Museum, Chicago, USA. Since 2011 MacArthur Associate Curator, Dept. of Botany, The Field Museum, Chicago, USA. 2006-2014 Associate Curator, Dept. of Botany, The Field Museum, Chicago, USA. 2005-2009 Head of Cryptogams, Dept. of Botany, The Field Museum, Chicago, USA. Since 2004 Member, Committee on Evolutionary Biology, University of Chicago. Courses: BIOS 430 Evolution (UIC), BIOS 23410 Complex Interactions: Coevolution, Parasites, Mutualists, and Cheaters (U of C) Reading group: Phylogenetic methods. 2003-2006 Assistant Curator, Dept. of Botany, The Field Museum, Chicago, USA. 1998-2003 Privatdozent (Assistant Professor), Botanical Institute, University – GHS - Essen. Lectures: General Botany, Evolution of lower plants, Photosynthesis, Courses: Cryptogams, Biology -
Mycokeysa Review 5: 1–30 Of(2012) the Genus Bulbothrix Hale: the Species with Medullary Salazinic Acid Lacking
A peer-reviewed open-access journal MycoKeysA review 5: 1–30 of(2012) the genus Bulbothrix Hale: the species with medullary salazinic acid lacking... 1 doi: 10.3897/mycokeys.5.3342 RESEARCH ARTICLE MycoKeys www.pensoft.net/journals/mycokeys Launched to accelerate biodiversity research A review of the genus Bulbothrix Hale: the species with medullary salazinic acid lacking vegetative propagules Michel N. Benatti1 1 Instituto de Botânica, Núcleo de Pesquisa em Micologia, Caixa Postal 68041, São Paulo / SP, CEP 04045- 972, Brazil Corresponding author: Michel N. Benatti ([email protected]) Academic editor: Pradeep Divakar | Received 7 May 2012 | Accepted 22 October 2012 | Published 31 October 2012 Citation: Benatti MN (2012) A review of the genus Bulbothrix Hale: the species with medullary salazinic acid lacking vegetative propagules. MycoKeys 5: 1–30. doi: 10.3897/mycokeys.5.3342 Abstract Descriptions are presented for the seven known Bulbothrix (Parmeliaceae, Lichenized Fungi) species with salazinic acid in the medulla and without vegetative propagules. Bulbothrix continua, previously consid- ered as a synonym of B. hypocraea, is recognized as independent species. The current delimitations are confirmed for B. enormis, B. hypocraea, B. meizospora, B. linteolocarpa, B. sensibilis, and B. setschwanensis. New characteriscs and range extensions are provided. Key words Parmeliaceae, Parmelinella, norstictic acid, bulbate cilia Introduction The genus Bulbothrix Hale was proposed for the group of species called Parmelia Se- ries Bicornutae (Lynge) Hale & Kurokawa (Hale 1974). This group is characterized by small, laciniate and usually adnate thalli, bulbate marginal cilia, an upper cortex con- taining atranorin, with pored epicortex, without pseudocyphellae, with isolichenan in the cell walls, simple to branched cilia and rhizinae, smooth to coronate apothecia, hya- line unicellular ellipsoid to bicornute ascospores 5.0−21.0 × 4.0−12.0 µm, and bacilli- form to bifusiform conidia 5.0−10.0× 0.5− 1.0 µm (Hale 1976a, Elix 1993, Elix 1994). -
Piedmont Lichen Inventory
PIEDMONT LICHEN INVENTORY: BUILDING A LICHEN BIODIVERSITY BASELINE FOR THE PIEDMONT ECOREGION OF NORTH CAROLINA, USA By Gary B. Perlmutter B.S. Zoology, Humboldt State University, Arcata, CA 1991 A Thesis Submitted to the Staff of The North Carolina Botanical Garden University of North Carolina at Chapel Hill Advisor: Dr. Johnny Randall As Partial Fulfilment of the Requirements For the Certificate in Native Plant Studies 15 May 2009 Perlmutter – Piedmont Lichen Inventory Page 2 This Final Project, whose results are reported herein with sections also published in the scientific literature, is dedicated to Daniel G. Perlmutter, who urged that I return to academia. And to Theresa, Nichole and Dakota, for putting up with my passion in lichenology, which brought them from southern California to the Traingle of North Carolina. TABLE OF CONTENTS Introduction……………………………………………………………………………………….4 Chapter I: The North Carolina Lichen Checklist…………………………………………………7 Chapter II: Herbarium Surveys and Initiation of a New Lichen Collection in the University of North Carolina Herbarium (NCU)………………………………………………………..9 Chapter III: Preparatory Field Surveys I: Battle Park and Rock Cliff Farm……………………13 Chapter IV: Preparatory Field Surveys II: State Park Forays…………………………………..17 Chapter V: Lichen Biota of Mason Farm Biological Reserve………………………………….19 Chapter VI: Additional Piedmont Lichen Surveys: Uwharrie Mountains…………………...…22 Chapter VII: A Revised Lichen Inventory of North Carolina Piedmont …..…………………...23 Acknowledgements……………………………………………………………………………..72 Appendices………………………………………………………………………………….…..73 Perlmutter – Piedmont Lichen Inventory Page 4 INTRODUCTION Lichens are composite organisms, consisting of a fungus (the mycobiont) and a photosynthesising alga and/or cyanobacterium (the photobiont), which together make a life form that is distinct from either partner in isolation (Brodo et al. -
An Update on the Genus Parmelinella Elix & Hale
Mycosphere 5 (6): 770–789(2014) ISSN 2077 7019 www.mycosphere.org Article Mycosphere Copyright © 2014 Online Edition Doi 10.5943/mycosphere/5/6/8 An update on the genus Parmelinella Elix & Hale (Parmeliaceae, lichenized Ascomycetes) Benatti MN1 1 Instituto de Botânica, Núcleo de Pesquisa em Micologia, Caixa Postal 68041, São Paulo / SP, CEP 04045-972, Brazil. E-mail: [email protected] Benatti MN 2014 – An update on the genus Parmelinella Elix & Hale (Parmeliaceae, lichenized ascomycetes). Mycosphere 5(6), 770–789, Doi 10.5943/mycosphere/5/6/8 Abstract A detailed morphological and anatomical investigation of the type specimens of the current- ly accepted species of Parmelinella (Parmeliaceae, Lichenized Fungi) confirmed the current spe- cies delimitations and revealed additional characteristics. The name Parmelia mutata is removed from synonymy with Parmelinella versiformis and proposed as a new combination, and Parmelia nimandairana is removed from Parmelinella wallichiana and proposed as another new combina- tion. Parmelinella salacinifera is proposed as a new combination. A lectotype is designated for Parmelinella versiformis. A key to all currently accepted species of the genus is presented. Key words – Canoparmelia – Parmelina – Parmotremopsis – cilia – salazinic acid Introduction Elix & Hale (1987) installed the genus Parmelinella for three species previously included in Parmelina (P. wallichiana, P. manipurensis and P. simplicior) with broad, rotund lobes, an emaculate thallus, sparse, simple cilia more or less restricted to the axils, simple black rhizines, ellipsoid ascospores, short cylindrical conidia, and salazinic and consalazinic acids in the medulla. A key for the differentiation of this and some further newly proposed genera, all segregates of Parmelina, and a table containing many characteristics for them was included with the descriptions of the genera. -
Abstracts for IAL 6- ABLS Joint Meeting (2008)
Abstracts for IAL 6- ABLS Joint Meeting (2008) AÐALSTEINSSON, KOLBEINN 1, HEIÐMARSSON, STARRI 2 and VILHELMSSON, ODDUR 1 1The University of Akureyri, Borgir Nordurslod, IS-600 Akureyri, Iceland, 2Icelandic Institute of Natural History, Akureyri Division, Borgir Nordurslod, IS-600 Akureyri, Iceland Isolation and characterization of non-phototrophic bacterial symbionts of Icelandic lichens Lichens are symbiotic organisms comprise an ascomycete mycobiont, an algal or cyanobacterial photobiont, and typically a host of other bacterial symbionts that in most cases have remained uncharacterized. In the current project, which focuses on the identification and preliminary characterization of these bacterial symbionts, the species composition of the resident associate microbiota of eleven species of lichen was investigated using both 16S rDNA sequencing of isolated bacteria growing in pure culture and Denaturing Gradient Gel Electrophoresis (DGGE) of the 16S-23S internal transcribed spacer (ITS) region amplified from DNA isolated directly from lichen samples. Gram-positive bacteria appear to be the most prevalent, especially actinomycetes, although bacilli were also observed. Gamma-proteobacteria and species from the Bacteroides/Chlorobi group were also observed. Among identified genera are Rhodococcus, Micrococcus, Microbacterium, Bacillus, Chryseobacterium, Pseudomonas, Sporosarcina, Agreia, Methylobacterium and Stenotrophomonas . Further characterization of selected strains indicated that most strains ar psychrophilic or borderline psychrophilic, -
Molecular Data Support Pseudoparmelia As a Distinct Lineage Related to Relicina and Relicinopsis (Ascomycota, Lecanorales)
The Lichenologist 47(1): 43–49 (2015) 6 British Lichen Society, 2015 doi:10.1017/S0024282914000577 Molecular data support Pseudoparmelia as a distinct lineage related to Relicina and Relicinopsis (Ascomycota, Lecanorales) Kawinnat BUARUANG, Klara SCHARNAGL, Pradeep DIVAKAR, Steven D. LEAVITT, Ana CRESPO, Thomas H. NASH, Leka MANOCH, Robert LU¨ CKING and H. Thorsten LUMBSCH Abstract: The phylogenetic position of the genus Pseudoparmelia was addressed using molecular data from five loci (mtSSU, nuLSU, ITS, Mcm7, RPB1), generated from three species and aligned with sequences from 293 samples representing all major clades of Parmeliaceae. Pseudoparmelia species form a well-supported monophyletic group that is the sister group of a clade consisting of the genera Relicina and Relicinopsis. These three genera share a thallus with a pored epicortex, isolichenan as cell wall polysaccharide, and relatively small ascospores. Morphological and chemical characters that distinguish Pseudoparmelia from the closely related Relicina and Relicinopsis are discussed. To further elucidate the relationships of these three genera, we assembled a second dataset including 15 addi- tional samples of Relicina and Relicinopsis using three loci (mtSSU, nuLSU, ITS). All three genera are monophyletic but monophyly of Relicina lacks support and, in the mtSSU single locus tree, the genus is paraphyletic with Relicinopsis nested within. Additional studies including more Relicina species are necessary to test delimitation of the genera Relicina and Relicinopsis. Key words: generic concept, lichens, molecular systematics, Parmeliaceae, parmelioid lichens, taxonomy Accepted for publication 9 October 2014 Introduction (Crespo et al. 2011; Thell et al. 2012). Pres- ently, the c. 2800 recognized species are clas- Molecular studies have helped to develop a sified into over 80 genera, the bulk of them new generic-level classification in the Parme- belonging to the parmelioid lichens. -
Field Oriented Keys to the Florida Lichens
Field oriented keys to the Florida lichens Roger Rosentreter, Ann M. DeBolt, & Barry Kaminsky December 12, 2015 Version Boise State University Field oriented keys to Florida Lichens Roger Rosentreter Department of Biology Boise State University 1910 University Drive Boise, ID 83725 [email protected] Barry Kaminsky University of Florida Gainesville, FL [email protected] [email protected] Ann DeBolt Natural Plant Communities Specialist Idaho Botanical Garden 2355 Old Penitentiary Rd. Boise, ID 83712 [email protected] [email protected] Table of Contents Introduction: Keys to genera and groups Keys to species Bulbothrix Candelaria Canoparmelia Cladonia Coccocarpia Coenogonium Collema see Leptogium key below. Crocynia Dirinaria Heterodermia Hyperphyscia Hypotrachyna Leptogium Lobaria Myelochroa Nephroma Normandina Pannaria Parmelinopsis Parmeliopsis Parmotrema Peltigera Phaeophyscia Physciella see Phaeophyscia key Physcia Physma Pseudocyphellaria Pseudoparmelia Punctelia Pyxine Ramalina Relicina Sticta Teloschistes Tuckermanella Usnea Vulpicida Xanthoparmelia Audience: Ecologists, Fieldwork technicians, Citizen Scientists, Naturalists, Lichenologists, general Botanists Potential Reviewers: Doug Ladd Rick Demmer Dr. Bruce McCune James Lendemer Richard Harris Introduction: There is still much to learn about Florida macrolichens. Macrolichen diversity was first catalogued by Moore (1968), followed by Harris (1990, 1995). “Lichens of North America” also contains photographs and descriptions of many of Florida’s macrolichens (Brodo et al. 2001). The aim of this book is to compliment these other resources and provide more field oriented keys to the macrolichen diversity. We hope to encourage the incorporation of lichens into field oriented ecological studies. Many of the species included in the keys are based lists and information from Harris (1990, 1995). In a few cases with a few rare Genera, Harris’ key very similar. -
<I>Hypotrachyna</I>
ISSN (print) 0093-4666 © 2012. Mycotaxon, Ltd. ISSN (online) 2154-8889 MYCOTAXON http://dx.doi.org/10.5248/119.157 Volume 119, pp. 157–166 January–March 2012 A new species and new combinations and records of Hypotrachyna and Remototrachyna from Bolivia Adam Flakus1, Pamela Rodriguez Saavedra2, 3 & Martin Kukwa4 1Laboratory of Lichenology, W. Szafer Institute of Botany, Polish Academy of Sciences, Lubicz 46, PL–31–512 Kraków, Poland 2Department of Botany and Molecular Evolution, Senckenberg Forschungsinstitut und Naturmuseum, Senckenberganlage 25, D-60325 Frankfurt am Main, Germany 3Herbario Nacional de Bolivia, Instituto de Ecología, Universidad Mayor de San Andrés, Calle 27, Cota Cota, Casilla 10077, La Paz, Bolivia 4Department of Plant Taxonomy and Nature Conservation, University of Gdańsk, Al. Legionów 9, PL–80–441 Gdańsk, Poland Correspondence to: 1a.fl[email protected], [email protected] & [email protected] Abstract — Remototrachyna sipmaniana is described as new to science, and three new combinations, R. aguirrei, R. consimilis, and R. singularis, are proposed. Ten Hypotrachyna and two Remototrachyna species are reported as new to Bolivia, including the southernmost localities of H. halei and H. partita, the first record of H. primitiva from the southern hemisphere, and the second locality for H. neoscytodes. Key words — foliose lichens, Neotropics, Parmeliaceae, South America Introduction Parmeliaceae Zenker (Lecanorales, Lecanoromycetes) is a large family of Ascomycota consisting of foliose, fruticose or rarely crustose lichens, but also lichenicolous non-lichenized taxa (e.g. Elix 1993, Lumbsch & Huhndorf 2007, Peršoh & Rambold 2002). It is believed to be one of the richest in species within the phylum and comprises about 1500 species (Blanco et al. -
Canoparmelia Cinerascens Belongs in the Genus Parmelinella (Parmeliaceae, Lichenized Ascomycota)
Opuscula Philolichenum, 11: 26-30. 2012. *pdf available online 3January2012 via (http://sweetgum.nybg.org/philolichenum/) Canoparmelia cinerascens belongs in the genus Parmelinella (Parmeliaceae, lichenized Ascomycota) 1 MICHEL NAVARRO BENATTI ABSTRACT. – Canoparmelia cinerascens, a species previously included in the genus Canoparmelia is actually a member of the genus Parmelinella. As such, the new combination Parmelinella cinerascens (Lynge) Benatti & Marcelli is proposed here. The species is described in detail and an epitype is selected to aid interpretation due the poor condition of the holotype. KEYWORDS. – Axillary cilia, Parmelinella wallichiana, salazinic acid INTRODUCTION Canoparmelia Elix & Hale, a segregate of the eciliate parmelioid lichen genus Pseudoparmelia Lynge (Hale 1976), is characterized by the typically gray or rarely yellow-green thalli containing cortical atranorin and chloroatranorin (or rarely usnic acid), the 3.05.0 mm rotund or subrotund eciliate lobes, the white medulla, the black lower surface with naked brown margins and simple concolorous rhizines, small ellipsoid ascospores 1014 68 m, and fusiform or bifusiform conidia 710 m in length (Elix 1993, Elix et al. 1986). When the genus Parmelinella was segregated from Parmelina Hale, only three species originally in Parmelina had been recombined into Parmelinella (Elix & Hale 1987). However, the species with small axillary cilia discussed in this paper was misplaced in Pseudoparmelia sensu Hale, and later automatically transferred to Canoparmelia. Working with -
Checklist of Georgia Lichens
Georgia Lichen Atlas Project Arthonia degelii Buellia caloosensis p Caloplaca granularis Arthonia interveniens Buellia curtisii Caloplaca holocarpa CHECKLIST Arthonia macrotheca Buellia elizae Caloplaca pollinii Arthonia montagnei Buellia imshaugiana Caloplaca saxicola of GEORGIA Arthonia quintaria Buellia lauricassiae Candelaria concolor Arthonia ruana Buellia maculata Candelaria fibrosa LICHENS Arthonia rubella Buellia mamillana Candelariella reflexa Arthopyrenia lyrata Buellia punctata Canoparmelia amazonica *non-lichenized, parasitic or lichenicolous fungus Arthrothelium spectabile Buellia spuria Canoparmelia caroliniana pprovisional status Aspicilia cinerea Buellia stillingiana Canoparmelia crozalsiana Date: Aspicilia contorta Buellia vernicoma Canoparmelia cryptochlorophaea Aspicilia verrucigera Buellia wheeleri Canoparmelia salacinifera Location: Aspicilia caesiocinerea Buelliella trypethelii* Canoparmelia texana Bacidia circumspecta Bulbothrix confoederata Carbonea latypizodes Lat/Long: Bacidia crenulata Bulbothrix goebelii Catillaria chalybeia Abrothallus cladoniae Bacidia diffracta Bulbothrix isidiza Cetradonia linearis Acarospora badiofusca Bacidia granosa Bulbothrix laevigatula Cetrelia chicitae Acarospora dispersa Bacidia heterochroa Byssoloma leucoblepharum Cetrelia olivetorum Acarospora fuscata Bacidia polychroa Byssoloma pubescens Chaenotheca brunneola Acarospora obpallens Bacidia rubella Calicium abietinum Chaenotheca furfuracea Agonimia opuntiella Bacidia schweinitzii Calicium glaucellum Chrysothrix flavovirens Ahtiana -
FLAVOPARMELIA John A.Elix [From Flora of Australia Volume 55 (1994)]
FLAVOPARMELIA John A.Elix [From Flora of Australia volume 55 (1994)] Flavoparmelia Hale, Mycotaxon 25: 604 (1986); from the Latin flavus (yellow), referring to the colour of the upper surface of this segregate of Parmelia. Type: F. caperata (L.) Hale Thallus foliose, loosely adnate to adnate, or rarely tightly adnate, dorsiventral, orbicular, to 3–20 cm wide. Lobes irregular, 1–8 mm wide; margins without cilia; apices rotund or subrotund, never incised. Upper surface yellow-green to green, rarely yellow (usnic acid and ±traces of atranorin), smooth, rugulose or rugose, without pseudocyphellae, with or without maculae, soralia, dactyls, pustules and isidia; upper cortex of palisade plectenchyma with a thin, pored epicortex. Cell walls containing isolichenan. Medulla white, or partly yellow or orange. Lower surface black, with a narrow, brown, naked marginal zone; rhizines sparse to moderately abundant, simple, tufted or rarely dichotomously branched, usually concolorous, often pale at lobe apices. Ascomata apothecial, laminal, sessile to subpedicellate, 1–10 mm wide; disc imperforate, shiny or matt, red-brown to cinnamon-brown or dark brown. Ascospores ellipsoidal, 8 per ascus, 12–21 × 5–11 µm. Conidiomata pycnidial, laminal, subglobose to globose, immersed; ostiole black. Conidia bifusiform, rarely fusiform or bacilliform, 4–12 × 1 µm. Flavoparmelia is a segregate of Parmelia s. lat. containing c. 22 species, of which 13 species occur in Australia. It is a common and widespread genus in Australia, occurring on rock, bark, dead wood and old fence posts. Several species are particularly common on the trunks and branches of Callitris, Casuarina and Allocasuarina in drier hinterland areas. M.E.Hale, A monograph of the lichen genus Pseudoparmelia Lynge (Parmeliaceae), Smithsonian Contr.