A Checklist of Lichens Collected During the First Howard Crum Bryological Workshop, Delaware Water Gap National Recreation Area
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Of the Sakhalin Island (Russian Far East) © 2021 Г
БОТАНИЧЕСКИЙ ЖУРНАЛ, 2021, том 106, № 2, с. 147–165 СООБЩЕНИЯ THE GENUS RINODINA (PHYSCIACEAE, LICHENIZED ASCOMYCOTA) OF THE SAKHALIN ISLAND (RUSSIAN FAR EAST) © 2021 г. I. A. Galanina1,*, A. K. Ezhkin2,**, and Y. Ohmura3,*** 1 Federal Scientific Center of East Asian Terrestrial Biodiversity, Far Eastern Branch of the Russian Academy of Sciences 100-letiya Vladivostoka Ave., 159, Vladivostok, 690024, Russia 2 Institute of Marine Geology and Geophysics, Far Eastern Branch of the Russian Academy of Sciences Nauki Str., 1B, Yuzhno-Sakhalinsk, 693022, Russia 3 Department of Botany, National Museum of Nature and Science 4-1-1 Amakubo, Tsukuba, Ibaraki, 305-0005, Japan *e-mail: [email protected] **e-mail: [email protected] ***e-mail: [email protected] Received February 27, 2020; Revised October 06, 2020; Accepted October 14, 2020 The presented work is based on the study of extensive material collected by A.K. Ezhkin in 2011–2018 from Sakhalin Island and herbarium specimens (VLA). As a result of the study, the new list of species of the genus Rinodina for Sakhalin Island consists 24 taxa. One species, Rinodina albertana Sheard, is new to Northeast Asia and Russia, 8 taxa are new to Sakhalin Island. The species are discussed with respect to their distribution in Northeast Asia and North America. Brief descriptions of rare species (R. albertana, R. bukii Sheard, and R. endospora Sheard) found on Sakhalin Island are made. The record of R. exigua (Ach.) Gray for Sakhalin Island (Galanina, 2013) belongs to R. freyi. Keywords: lichens, Physciaceae, biodiversity, endemism, distribution, Northeast Asia, North America DOI: 10.31857/S0006813621020034 INTRODUCTION ter than the adjacent continent, and with a cool rainy summer. -
Australasian Lichenology Number 56, January 2005
Australasian Lichenology Number 56, January 2005 Australasian Lichenology Number 56, January 2005 ISSN 1328-4401 The Austral Pannaria immixta c.olonizes rock, bark, and occasionally bryophytes in both shaded and well-lit humid lowlands. Its two most distinctive traits are its squamulose thallus and its gyrose apothecial discs. 1 mm c:::::===- CONTENTS NEWS Kantvilas, ~ack Elix awarded the Acharius medal at IAL5 2 BOOK REVIEW Galloway, DJ-The Lichen Hunters, by Oliver Gilbert (2004) 4 RECENT LITERATURE ON AUSTRALASIAN LICHENS 7 ADDITIONAL LICHEN RECORDS FROM AUSTRALIA Elix, JA; Lumbsch, HT (55)-Diploschistes conception is 8 ARTICLES Archer, AW-Australian species in the genus Diorygma (Graphidaceae) ....... 10 Elix, JA; Blanco, 0; Crespo, A-A new species of Flauoparmelia (Parmeliaceae, lichenized Ascomycota) from Western Australia ...... .... ............................ ...... 12 Galloway, DJ; Sancho, LG-Umbilicaria murihikuana and U. robusta (Umbili cariaceae: Ascomycota), two new taxa from Aotearoa New Zealand .. ... .. ..... 16 Elix, JA; Bawingan, PA; Lardizaval, M; Schumm, F-Anew species ofMenegazzia (Parmeliaceae, lichenized Ascomycota) and new records of Parmeliaceae from Papua New Guinea and the Philippines .................................. .. .................... 20 Malcolm, WM-'ITansfer ofDimerella rubrifusca to Coenogonium ........ ......... 25 Johnson, PN- Lichen succession near Arthur's Pass, New Zealand ............... 26 NEWS JACK ELIXAWARDED THE ACHARIUS MEDALAT IAL5 The recent Fifth Conference of the International Association for Lichenology (1AL5) in Tartu, Estonia, was a highly successful event, and most Australasian lichenologists will have the opportunity to read of its various academic achieve ments in other media*. The social programme included the traditionallAL Din ner, where, after many days of symposia, poster sessions, excursions, meetings and other lichenological events, conference delegates mingle informally and dust away their weariness over food and drink. -
A New Checklist of Lichenised, Lichenicolous and Allied Fungi Reported from South Africa
Page 1 of 4 Original Research A new checklist of lichenised, lichenicolous and allied fungi reported from South Africa Author: Background: The last comprehensive list of lichenised, lichenicolous and allied fungi reported 1 Alan M. Fryday from South Africa was published in 1950. A checklist is important to provide basic information Affiliation: on the extent of the diversity, and to provide the most recent name and classification. 1Department of Plant Biology, Michigan State University, Objective: To present a list of all the lichenised, lichenicolous and allied fungi reported from United States South Africa. Correspondence to: Methods: The list presented is entirely literature based and no attempt has been made to Alan Fryday check the report of any taxa or their status by checking the specimens upon which they are based. Firstly, all taxa that were not reported from within the modern boundaries of South Email: Africa were excluded. Next, the Recent literature on lichens database was searched for literature [email protected] on South African lichens since 1945 and all references checked for new species or new reports, Postal address: which were then added to the list. These names were then checked against Index Fungorum Department of Plant Biology, to ensure that the most current name was being used. Finally, the list was rationalised by Plant Biology Laboratories, 612 Wilson Road, East excluding all synonyms and dubious infraspecific taxa. Lansing, MI, 48824, Results: The current list includes 1750 taxa in 260 genera from mainland South Africa, with United States an additional 100 species and 23 genera from the sub-Antarctic Prince Edward Islands, which Dates: are treated separately. -
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 -
Habitat Quality and Disturbance Drive Lichen Species Richness in a Temperate Biodiversity Hotspot
Oecologia (2019) 190:445–457 https://doi.org/10.1007/s00442-019-04413-0 COMMUNITY ECOLOGY – ORIGINAL RESEARCH Habitat quality and disturbance drive lichen species richness in a temperate biodiversity hotspot Erin A. Tripp1,2 · James C. Lendemer3 · Christy M. McCain1,2 Received: 23 April 2018 / Accepted: 30 April 2019 / Published online: 15 May 2019 © Springer-Verlag GmbH Germany, part of Springer Nature 2019 Abstract The impacts of disturbance on biodiversity and distributions have been studied in many systems. Yet, comparatively less is known about how lichens–obligate symbiotic organisms–respond to disturbance. Successful establishment and development of lichens require a minimum of two compatible yet usually unrelated species to be present in an environment, suggesting disturbance might be particularly detrimental. To address this gap, we focused on lichens, which are obligate symbiotic organ- isms that function as hubs of trophic interactions. Our investigation was conducted in the southern Appalachian Mountains, USA. We conducted complete biodiversity inventories of lichens (all growth forms, reproductive modes, substrates) across 47, 1-ha plots to test classic models of responses to disturbance (e.g., linear, unimodal). Disturbance was quantifed in each plot using a standardized suite of habitat quality variables. We additionally quantifed woody plant diversity, forest density, rock density, as well as environmental factors (elevation, temperature, precipitation, net primary productivity, slope, aspect) and analyzed their impacts on lichen biodiversity. Our analyses recovered a strong, positive, linear relationship between lichen biodiversity and habitat quality: lower levels of disturbance correlate to higher species diversity. With few exceptions, additional variables failed to signifcantly explain variation in diversity among plots for the 509 total lichen species, but we caution that total variation in some of these variables was limited in our study area. -
BLS Bulletin 111 Winter 2012.Pdf
1 BRITISH LICHEN SOCIETY OFFICERS AND CONTACTS 2012 PRESIDENT B.P. Hilton, Beauregard, 5 Alscott Gardens, Alverdiscott, Barnstaple, Devon EX31 3QJ; e-mail [email protected] VICE-PRESIDENT J. Simkin, 41 North Road, Ponteland, Newcastle upon Tyne NE20 9UN, email [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: S. -
Rinodina Fuscoisidiata, a New Muscicolous, Isidiate Species from Venezuela
The Lichenologist 42(1): 73–76 (2010) © British Lichen Society, 2009 doi:10.1017/S0024282909990193 Rinodina fuscoisidiata, a new muscicolous, isidiate species from Venezuela Mireia GIRALT, Klaus KALB and John A. ELIX Abstract: Rinodina fuscoisidiata, a muscicolous isidiate species with large isidia and Pachysporaria-type ascospores is described from Venezuela. This species contains an unknown terpene as a major secondary metabolite in addition to traces of atranorin. It is compared with the four known isidiate Rinodina taxa. Key words: South America, taxonomy, lichenized fungi, Physciaceae, Lecanoromycetes Introduction Materials and Methods While revising the species of the genus The specimens were examined by standard techniques Rinodina (Ach.) Gray belonging to the using stereoscopic and compound microscopes. Current mycological terminology generally follows Kirk et al. Dolichospora group (at present including R. (2001). Only free ascospores lying outside the asci have brasiliensis Giralt, Kalb & H. Mayrhofer,R. been measured. Measurements were made in water at dolichospora Malme, R. guianensis Aptroot, ×1000 magnification. Mean value (x) and standard de- R. intermedia Bagl. and R. inspersoparietata viation (SD) were calculated and the results are given as Giralt & van den Boom), typically character- (minimum value observed) x ± SD (maximum value observed) followed by x,SDandn (the total number of ized by containing drops of uncertain origin ascospores measured) in parentheses. The terminology and nature surrounding the lumina of the used for the asci follows Rambold et al. (1994) and for ascospores (Giralt et al. 2008, 2009), we the ascospore-types and ascospore-ontogenies Giralt examined several muscicolous, isidiate Rino- (2001). Chemical constituents were identified by thin- layer chromatography (TLC) and high performance dina specimens from Venezuela collected at liquid chromatography (HPLC) (Elix et al. -
Ph.D. Thesis Presented to the University of Lordon January, 1966
Ph.D. thesis presented to the University of Lordon January, 1966. 3. A. revision of the lichen genus Liman* in Europe and its taxonomic, affinities J. qr. Sheard, V.So., D.I.C., Department of Botany, Imperial College, London 501.7. 2 t Abstract A partial revision of the genus Rinodina in Europe has been undertaken. 96 species have been studied and 41 of these have been reduced to synonomy. The remaining 50 species include speolespalasdtimp) new to science and 2 new combinations. This revision has been carried out with the aid of more refined sectioning and optical equipment than was available to previous workers and with a greater knowledge of the effects of environ- mental modification. The author has also attempted, to apply modern taxonomic principles during the studies and recent dis- coveries regarding the onotgeny and range of form of the apotheeha have also helped in defining the limits of related genera. The subdivision of the genus has been redefined using the spore structure, rather than the spore septation and tballus morphology, as the principle criterion. The relational*p of the genus Rinodim with the other genera of the Bue=awe, end rivaciacea, has also been examined. It has tentatively been suggested that two genera be redesaribed; the genus k4ismajaQi5 to accommodate certain species previously, placed in BuoUi or Rim Klima, end the monospeoifio genus Dita,010141 previously placed under %Lelia, to be transferred to the Plysataoeao. 3. introduotion 5 The problem 5 Historical review 6 Review of lichen taxonomy with particular reference to the genus Ameba 6 Classification' within the Suellitaceae and aainaidatfa 9 Basis of revision and limits of work 15 Materials and methods 16 Herbaria consulted 16 Sectioning and preparation of material for detailed examination ' 17 Reagents and mounting fluids used 18 Apparatus used. -
Lichens and Allied Fungi of the Indiana Forest Alliance
2017. Proceedings of the Indiana Academy of Science 126(2):129–152 LICHENS AND ALLIED FUNGI OF THE INDIANA FOREST ALLIANCE ECOBLITZ AREA, BROWN AND MONROE COUNTIES, INDIANA INCORPORATED INTO A REVISED CHECKLIST FOR THE STATE OF INDIANA James C. Lendemer: Institute of Systematic Botany, The New York Botanical Garden, Bronx, NY 10458-5126 USA ABSTRACT. Based upon voucher collections, 108 lichen species are reported from the Indiana Forest Alliance Ecoblitz area, a 900 acre unit in Morgan-Monroe and Yellowwood State Forests, Brown and Monroe Counties, Indiana. The lichen biota of the study area was characterized as: i) dominated by species with green coccoid photobionts (80% of taxa); ii) comprised of 49% species that reproduce primarily with lichenized diaspores vs. 44% that reproduce primarily through sexual ascospores; iii) comprised of 65% crustose taxa, 29% foliose taxa, and 6% fruticose taxa; iv) one wherein many species are rare (e.g., 55% of species were collected fewer than three times) and fruticose lichens other than Cladonia were entirely absent; and v) one wherein cyanolichens were poorly represented, comprising only three species. Taxonomic diversity ranged from 21 to 56 species per site, with the lowest diversity sites concentrated in riparian corridors and the highest diversity sites on ridges. Low Gap Nature Preserve, located within the study area, was found to have comparable species richness to areas outside the nature preserve, although many species rare in the study area were found only outside preserve boundaries. Sets of rare species are delimited and discussed, as are observations as to the overall low abundance of lichens on corticolous substrates and the presence of many unhealthy foliose lichens on mature tree boles. -
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, -
Opuscula Philolichenum, 6: 1-XXXX
Opuscula Philolichenum, 14: 121-138. 2015. *pdf effectively published online 2October2015 via (http://sweetgum.nybg.org/philolichenum/) Lichen Diversity in Southeast Iowa 1 2 AMY L. PODARIL & JAMES T. COLBERT ABSTRACT. – Exploration of the lichen diversity in southeast Iowa has historically been limited. Prior to this study only 124 of the total 7,644 known specimens of Iowa lichens (1.6%) were from four counties in southeast Iowa. After two years of field work a total of 150 species were identified from 395 specimens, 18 of which are new records for the state. Only 29 of the species found had been previously documented in southeastern Iowa. Integration of these collecting efforts with previous efforts provides an estimate of 465 species of lichens reported for Iowa. Of these species, 33 macrolichen species are likely to be rare in, or extirpated from, the state. KEYWORDS. – Biodiversity, Great Plains, North America, land use change, United States. INTRODUCTION Iowa has undergone severe landscape alterations since European settlement in the early 1800’s. In the 1830’s, Iowa was covered in 28 million acres of tallgrass prairie mixed with wetlands and 7 million acres of forest (Johnson 2000). Between 1832 and 1875 forests of the state fell to fewer than 2.6 million acres (Cohen 1992). Virtually all of the current forested land in Iowa is second or third growth with very little or no old growth forest remaining in the state (Johnson 2000). Plowing of more than 99.9% of the 28 million acres of tallgrass prairie in the state began in the 1850’s, along with conversion of 95% of prairie wetlands to agricultural use by 1970 (Cohen and Iowa Association of Naturalists 1992). -
Red List of Estonian Lichens: Revision in 2019
Folia Cryptog. Estonica, Fasc. 56: 63–76 (2019) https://doi.org/10.12697/fce.2019.56.07 Red List of Estonian lichens: revision in 2019 Piret Lõhmus1, Liis Marmor2, Inga Jüriado1, Ave Suija1,3, Ede Oja1, Polina Degtjarenko1,4, Tiina Randlane1 1University of Tartu, Institute of Ecology and Earth Sciences, Lai 40, 51005 Tartu, Estonia. E-mail: [email protected] 2E-mail: [email protected] 3University of Tartu, Natural History Museum, Vanemuise 46, 51014 Tartu, Estonia 4Swiss Federal Research Institute WSL, Biodiversity and Conservation Biology, Zürcherstrasse 111, 8903 Birmensdorf, Switzerland Abstract: The second assessment of the threat status of Estonian lichens based on IUCN system was performed in 2019. The main basis for choosing the species to be currently assessed was the list of legally protected lichens and the list of species assigned to the Red List Categories RE–DD in 2008. Species that had been assessed as Least Concern (LC) in 2008 were not evaluated. Altogether, threat status of 229 lichen species was assessed, among them 181 were assigned to the threatened categories (CR, EN, VU), while no species were assigned to the LC category. Compared to the previous red list, category was deteriorated for 58% and remained the same for 32% of species. In Estonia, threatened lichens inhabit mainly forests (particularly dry boreal and nemoral deciduous stands), alvar grasslands, sand dunes and various saxicolous habitats. Therefore, the most frequent threat factors were forest cutting and overgrowing of alvars and dunes (main threat factor for 96 and 70 species, respectfully). Kokkuvõte: 2019. aastal viidi läbi teistkordne IUCN süsteemil põhinev Eesti samblike ohustatuse hindamine.