An Updated List of Mosses of Korea
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A Revision of Schoenobryum (Cryphaeaceae, Bryopsida) in Africa1
Revision of Schoenobryum 147 Tropical Bryology 24: 147-159, 2003 A revision of Schoenobryum (Cryphaeaceae, Bryopsida) in Africa1 Brian J. O’Shea 141 Fawnbrake Avenue, London SE24 0BG, U.K. Abstract. The nine species and two varieties of Schoenobryum reported for Africa were investigated, and no characters were found that uniquely identified any of the taxa to be other than the pantropical Schoenobryum concavifolium. The following nine names become new synonyms of S. concavifolium: Cryphaea madagassa, C. subintegra, Acrocryphaea robusta, A. latifolia, A. subrobusta, A. tisserantii, A. latifolia var. microspora, A. plicatula and A. subintegra var. idanreense; a lectotype is selected for Acrocryphaea latifolia var. microspora P.de la Varde. INTRODUCTION as the majority have not been examined since the type description, and many have never been A recent checklist of Sub-Saharan Africa illustrated. (O’Shea, 1999) included nine species and two varieties of Schoenobryum, most of quite limited The purpose of this paper is to provide an distribution. Recent collecting in both Malawi overview of the genus worldwide, and to review (O’Shea et al., 2001) and Uganda (Wigginton et the taxonomic position of the African taxa. al., 2001) has shown the genus to be not uncommon, although there was only one CRYPHAEACEAE SCHIMP. 1856. previously published collection from the two countries (O’Shea, 1993). Apart from one Cryphaeaceae Schimp., Coroll. Bryol. Eur. 97. African taxon occurring in nine countries, the 1856 [‘1855’]. Type: Cryphaea D.Mohr in other 10 occurred in an average of 1.7 countries. F.Weber This particular profile is typical of unrevised genera in Africa, and indicative of a possible A brief review of the circumscription and need for revision (O’Shea, 1997), particularly systematics of the family, and the distinctions from related families (e.g. -
Fossil Mosses: What Do They Tell Us About Moss Evolution?
Bry. Div. Evo. 043 (1): 072–097 ISSN 2381-9677 (print edition) DIVERSITY & https://www.mapress.com/j/bde BRYOPHYTEEVOLUTION Copyright © 2021 Magnolia Press Article ISSN 2381-9685 (online edition) https://doi.org/10.11646/bde.43.1.7 Fossil mosses: What do they tell us about moss evolution? MicHAEL S. IGNATOV1,2 & ELENA V. MASLOVA3 1 Tsitsin Main Botanical Garden of the Russian Academy of Sciences, Moscow, Russia 2 Faculty of Biology, Lomonosov Moscow State University, Moscow, Russia 3 Belgorod State University, Pobedy Square, 85, Belgorod, 308015 Russia �[email protected], https://orcid.org/0000-0003-1520-042X * author for correspondence: �[email protected], https://orcid.org/0000-0001-6096-6315 Abstract The moss fossil records from the Paleozoic age to the Eocene epoch are reviewed and their putative relationships to extant moss groups discussed. The incomplete preservation and lack of key characters that could define the position of an ancient moss in modern classification remain the problem. Carboniferous records are still impossible to refer to any of the modern moss taxa. Numerous Permian protosphagnalean mosses possess traits that are absent in any extant group and they are therefore treated here as an extinct lineage, whose descendants, if any remain, cannot be recognized among contemporary taxa. Non-protosphagnalean Permian mosses were also fairly diverse, representing morphotypes comparable with Dicranidae and acrocarpous Bryidae, although unequivocal representatives of these subclasses are known only since Cretaceous and Jurassic. Even though Sphagnales is one of two oldest lineages separated from the main trunk of moss phylogenetic tree, it appears in fossil state regularly only since Late Cretaceous, ca. -
Plant Life MagillS Encyclopedia of Science
MAGILLS ENCYCLOPEDIA OF SCIENCE PLANT LIFE MAGILLS ENCYCLOPEDIA OF SCIENCE PLANT LIFE Volume 4 Sustainable Forestry–Zygomycetes Indexes Editor Bryan D. Ness, Ph.D. Pacific Union College, Department of Biology Project Editor Christina J. Moose Salem Press, Inc. Pasadena, California Hackensack, New Jersey Editor in Chief: Dawn P. Dawson Managing Editor: Christina J. Moose Photograph Editor: Philip Bader Manuscript Editor: Elizabeth Ferry Slocum Production Editor: Joyce I. Buchea Assistant Editor: Andrea E. Miller Page Design and Graphics: James Hutson Research Supervisor: Jeffry Jensen Layout: William Zimmerman Acquisitions Editor: Mark Rehn Illustrator: Kimberly L. Dawson Kurnizki Copyright © 2003, by Salem Press, Inc. All rights in this book are reserved. No part of this work may be used or reproduced in any manner what- soever or transmitted in any form or by any means, electronic or mechanical, including photocopy,recording, or any information storage and retrieval system, without written permission from the copyright owner except in the case of brief quotations embodied in critical articles and reviews. For information address the publisher, Salem Press, Inc., P.O. Box 50062, Pasadena, California 91115. Some of the updated and revised essays in this work originally appeared in Magill’s Survey of Science: Life Science (1991), Magill’s Survey of Science: Life Science, Supplement (1998), Natural Resources (1998), Encyclopedia of Genetics (1999), Encyclopedia of Environmental Issues (2000), World Geography (2001), and Earth Science (2001). ∞ The paper used in these volumes conforms to the American National Standard for Permanence of Paper for Printed Library Materials, Z39.48-1992 (R1997). Library of Congress Cataloging-in-Publication Data Magill’s encyclopedia of science : plant life / edited by Bryan D. -
Moss Occurrences in Yugyd Va National Park, Subpolar and Northern Urals, European North-East Russia
Biodiversity Data Journal 7: e32307 doi: 10.3897/BDJ.7.e32307 Data Paper Moss occurrences in Yugyd Va National Park, Subpolar and Northern Urals, European North-East Russia Galina Zheleznova‡, Tatyana Shubina‡, Svetlana Degteva‡‡, Ivan Chadin , Mikhail Rubtsov‡ ‡ Institute of Biology of Komi Scientific Centre of the Ural Branch of the Russian Academy of Sciences, Syktyvkar, Russia Corresponding author: Tatyana Shubina ([email protected]) Academic editor: Yasen Mutafchiev Received: 10 Dec 2018 | Accepted: 25 Mar 2019 | Published: 01 Apr 2019 Citation: Zheleznova G, Shubina T, Degteva S, Chadin I, Rubtsov M (2019) Moss occurrences in Yugyd Va National Park, Subpolar and Northern Urals, European North-East Russia. Biodiversity Data Journal 7: e32307. https://doi.org/10.3897/BDJ.7.e32307 Abstract Background This study produced a dataset containing information on moss occurrences in the territory of Yugyd Va National Park, located in the Subpolar and Northern Urals, European North- East Russia. The dataset summarises occurrences noted by long-term bryological explorations in remote areas of the Subpolar and Northern Urals from 1943 to 2015 and from studies published since 1915. The dataset consists of 4,120 occurrence records. The occurrence data were extracted from herbarium specimen labels (3,833 records) and data from published literature (287 records). Most of the records (4,104) are georeferenced. A total of 302 moss taxa belonging to 112 genera and 36 families are reported herein to occur in Yugyd Va National Park. The diversity of bryophytes in this National Park has not yet been fully explored and further exploration will lead to more taxa. -
Molecular Phylogeny of Chinese Thuidiaceae with Emphasis on Thuidium and Pelekium
Molecular Phylogeny of Chinese Thuidiaceae with emphasis on Thuidium and Pelekium QI-YING, CAI1, 2, BI-CAI, GUAN2, GANG, GE2, YAN-MING, FANG 1 1 College of Biology and the Environment, Nanjing Forestry University, Nanjing 210037, China. 2 College of Life Science, Nanchang University, 330031 Nanchang, China. E-mail: [email protected] Abstract We present molecular phylogenetic investigation of Thuidiaceae, especially on Thudium and Pelekium. Three chloroplast sequences (trnL-F, rps4, and atpB-rbcL) and one nuclear sequence (ITS) were analyzed. Data partitions were analyzed separately and in combination by employing MP (maximum parsimony) and Bayesian methods. The influence of data conflict in combined analyses was further explored by two methods: the incongruence length difference (ILD) test and the partition addition bootstrap alteration approach (PABA). Based on the results, ITS 1& 2 had crucial effect in phylogenetic reconstruction in this study, and more chloroplast sequences should be combinated into the analyses since their stability for reconstructing within genus of pleurocarpous mosses. We supported that Helodiaceae including Actinothuidium, Bryochenea, and Helodium still attributed to Thuidiaceae, and the monophyletic Thuidiaceae s. lat. should also include several genera (or species) from Leskeaceae such as Haplocladium and Leskea. In the Thuidiaceae, Thuidium and Pelekium were resolved as two monophyletic groups separately. The results from molecular phylogeny were supported by the crucial morphological characters in Thuidiaceae s. lat., Thuidium and Pelekium. Key words: Thuidiaceae, Thuidium, Pelekium, molecular phylogeny, cpDNA, ITS, PABA approach Introduction Pleurocarpous mosses consist of around 5000 species that are defined by the presence of lateral perichaetia along the gametophyte stems. Monophyletic pleurocarpous mosses were resolved as three orders: Ptychomniales, Hypnales, and Hookeriales (Shaw et al. -
<I>Barbula</I> (Musci: Pottiaceae)
TAXON 62 (1) • February 2013: 21–39 Kučera & al. • Hydrogonium, Streblotrichum, and Gymnobarbula gen. nov. SYSTEMATICS AND PHYLOGENY Partial generic revision of Barbula (Musci: Pottiaceae): Re-establishment of Hydrogonium and Streblotrichum, and the new genus Gymnobarbula Jan Kučera,1 Jiří Košnar1 & Olaf Werner2 1 Department of Botany, Faculty of Science, University of South Bohemia, Branišovská 31, 370 05 České Budějovice, Czech Republic 2 Departamento de Biología Vegetal (Botánica), Universidad de Murcia, Campus de Espinardo, 30100 Murcia, Spain Author for correspondence: Jan Kučera, [email protected] Abstract Large genera, that were defined using a restricted suite of morphological characters, are particularly prone to be polyphyletic. We analysed a representative selection of species traditionally assigned to the genus Barbula, believed to represent the largest genus of the moss family Pottiaceae, but which recently was suggested to be polyphyletic. Special attention was paid to species traditionally assigned to Barbula sect. Hydrogonium and sect. Convolutae, in which phylogenetic relationships are likely to be incongruent with morphological traits, which could have evolved in adaptation to hydric and otherwise extreme habitats. Our phylogenetic analysis was based on nrITS and chloroplast rps4 and trnM-trnV sequence data and resolved only the type of the genus, B. unguiculata, plus B. orizabensis, in subfamily Pottioideae, while most of the species occurring in the Northern Hemisphere are part of Trichostomoideae and need to be recognized within the reestablished and partly redefined genera Hydrogonium and Streblotrichum. The phylogenetically and morphologically divergent B. bicolor needs to be removed from Streblotrichum to a newly described genus, Gymnobarbula. Numerous taxonomic changes and nomenclatural novelties, resulting from the molecular, morphological and nomenclatural studies are proposed for taxa of Hydrogonium, particularly within the H. -
Hypnaceaeandpossiblyrelatedfn
Hikobial3：645-665.2002 Molecularphylo窪enyOfhypnobrJ/aleanmOssesasin化rredfroma lar淫e-scaledatasetofchlOroplastlｂｃＬ，withspecialre他rencetothe HypnaceaeandpOssiblyrelatedfnmilies1 HIRoMITsuBoTA，ＴｏＭｏＴｓｕＧｕＡＲＩＫＡｗＡ，ＨＩＲｏＹｕＫＩＡＫＩＹＡＭＡ，ＥＦＲＡＩＮＤＥＬｕＮＡ，DoLoREs GoNzALEz,MASANoBuHIGucHIANDHIRoNoRIDEGucHI TsuBoTA,Ｈ､,ARIKAwA,Ｔ,AKIYAMA,Ｈ,,ＤＥＬｕＮＡ,Ｅ,GoNzALEz,，.,HIGucHI,Ｍ ４ ＆DEGucHI，Ｈ、2002.Ｍolecularphylogenyofhypnobryaleanmossesasinferred fiPomalarge-scaledatasetofchloroplastr6cL,ｗｉｔｈspecialreferencetotheHypnaceae andpossiblyrelatedfamiliesl3:645-665． ▲ Phylogeneticrelationshipswithinthehypnobryaleanmosses(ｉｅ,theHypnales,Leuco- dontales,andHookeriales）havebeenthefbcusofmuchattentioninrecentyears Herewepresentphylogeneticinfierencesonthislargeclade，andespeciallyonthe Hypnaceaeandpossiblyrelatedftlmilies，basedonmaximumlikelihoodanalysisof l81r6cLsequences、Oursmdycorroboratesthat（１）theHypnales(ｓｓｔｒ.[＝sensu Vittl984])andLeucodontalesareeachnotmonophyleticentities、TheHypnalesand LeucodontalestogethercompriseawellsupportedsistercladetotheHookeriales;(2) theSematophyllaceae(s」at［＝sensuTsubotaetaL2000,2001a,ｂ])andPlagiothecia‐ ceae(s・str.［＝sensupresentDareeachresolvedasmonophyleticgroups,whileno particularcladeaccommodatesallmembersoftheHypnaceaeandCryphaeaceae;ａｎｄ (3)theHypnaceaeaswellasitstypegenusﾉﾘDlwz"川tselfwerepolyphyletioThese resultsdonotconcurwiththesystemsofVitt(1984)andBuckandVitt(1986),who suggestedthatthegroupswithasinglecostawouldhavedivergedfiFomthehypnalean ancestoratanearlyevolutionarystage，fbllowedbythegroupswithadoublecosta (seealsoTsubotaetall999;Bucketal2000）OurresultsfiPomlikelihoodanalyses -
Volume 1, Chapter 2-7: Bryophyta
Glime, J. M. 2017. Bryophyta – Bryopsida. Chapt. 2-7. In: Glime, J. M. Bryophyte Ecology. Volume 1. Physiological Ecology. Ebook 2-7-1 sponsored by Michigan Technological University and the International Association of Bryologists. Last updated 10 January 2019 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology/>. CHAPTER 2-7 BRYOPHYTA – BRYOPSIDA TABLE OF CONTENTS Bryopsida Definition........................................................................................................................................... 2-7-2 Chromosome Numbers........................................................................................................................................ 2-7-3 Spore Production and Protonemata ..................................................................................................................... 2-7-3 Gametophyte Buds.............................................................................................................................................. 2-7-4 Gametophores ..................................................................................................................................................... 2-7-4 Location of Sex Organs....................................................................................................................................... 2-7-6 Sperm Dispersal .................................................................................................................................................. 2-7-7 Release of Sperm from the Antheridium..................................................................................................... -
Part 2 – Fruticose Species
Appendix 5.2-1 Vegetation Technical Appendix APPENDIX 5.2‐1 Vegetation Technical Appendix Contents Section Page Ecological Land Classification ............................................................................................................ A5.2‐1‐1 Geodatabase Development .............................................................................................. A5.2‐1‐1 Vegetation Community Mapping ..................................................................................... A5.2‐1‐1 Quality Assurance and Quality Control ............................................................................ A5.2‐1‐3 Limitations of Ecological Land Classification .................................................................... A5.2‐1‐3 Field Data Collection ......................................................................................................... A5.2‐1‐3 Supplementary Results ..................................................................................................... A5.2‐1‐4 Rare Vegetation Species and Rare Ecological Communities ........................................................... A5.2‐1‐10 Supplementary Desktop Results ..................................................................................... A5.2‐1‐10 Field Methods ................................................................................................................. A5.2‐1‐16 Supplementary Results ................................................................................................... A5.2‐1‐17 Weed Species -
An Annotated Checklist of Tasmanian Mosses
15 AN ANNOTATED CHECKLIST OF TASMANIAN MOSSES by P.I Dalton, R.D. Seppelt and A.M. Buchanan An annotated checklist of the Tasmanian mosses is presented to clarify the occurrence of taxa within the state. Some recently collected species, for which there are no published records, have been included. Doubtful records and excluded speciei. are listed separately. The Tasmanian moss flora as recognised here includes 361 species. Key Words: mosses, Tasmania. In BANKS, M.R. et al. (Eds), 1991 (3l:iii): ASPECTS OF TASMANIAN BOTANY -- A TR1BUn TO WINIFRED CURTIS. Roy. Soc. Tasm. Hobart: 15-32. INTRODUCTION in recent years previously unrecorded species have been found as well as several new taxa described. Tasmanian mosses received considerable attention We have assigned genera to families followi ng Crosby during the early botanical exploration of the antipodes. & Magill (1981 ), except where otherwise indicated in One of the earliest accounts was given by Wilson (1859), the case of more recent publications. The arrangement who provided a series of descriptions of the then-known of families, genera and species is in alphabetic order for species, accompanied by coloured illustrations, as ease of access. Taxa known to occur in Taslnania ami Part III of J.D. Hooker's Botany of the Antarctic its neighbouring islands only are listed; those for Voyage. Although there have been a number of papers subantarctic Macquarie Island (politically part of since that time, two significant compilations were Tasmania) are not treated and have been presented published about the tum of the century. The first was by elsewhere (Seppelt 1981). -
Kenai National Wildlife Refuge Species List, Version 2018-07-24
Kenai National Wildlife Refuge Species List, version 2018-07-24 Kenai National Wildlife Refuge biology staff July 24, 2018 2 Cover image: map of 16,213 georeferenced occurrence records included in the checklist. Contents Contents 3 Introduction 5 Purpose............................................................ 5 About the list......................................................... 5 Acknowledgments....................................................... 5 Native species 7 Vertebrates .......................................................... 7 Invertebrates ......................................................... 55 Vascular Plants........................................................ 91 Bryophytes ..........................................................164 Other Plants .........................................................171 Chromista...........................................................171 Fungi .............................................................173 Protozoans ..........................................................186 Non-native species 187 Vertebrates ..........................................................187 Invertebrates .........................................................187 Vascular Plants........................................................190 Extirpated species 207 Vertebrates ..........................................................207 Vascular Plants........................................................207 Change log 211 References 213 Index 215 3 Introduction Purpose to avoid implying -
Annales Botanici Fennici 36: 265-269
Ann. Bot. Fennici 36: 265–269 ISSN 0003-3847 Helsinki 14 December 1999 © Finnish Zoological and Botanical Publishing Board 1999 Bryophyte flora of the Huon Peninsula, Papua New Guinea. LXVII. Amphidium (Rhabdoweisiaceae, Musci) Daniel H. Norris & Timo Koponen Norris, D. H. & Koponen, T., Department of Ecology and Systematics, Division of Systematic Biology, P.O. Box 7, FIN-00014 University of Helsinki, Finland Received 18 August 1999, accepted 1 November 1999 Norris, D. H. & Koponen, T. 1999: Bryophyte flora of the Huon Peninsula, Papua New Guinea. LXVII. Amphidium (Rhabdoweisiaceae, Musci). — Ann. Bot. Fennici 36: 265–269. Amphidium tortuosum (Hornsch.) Cufod. is the only species of the family Rhabdowei- siaceae occurring in Western Melanesia and New Guinea. Both collections came from cliff walls, one of them was in an open grassland area and the other in closed montane rainforest. The placement of Amphidium Schimp. in the neighbourhood of Dicranaceae and in the family Rhabdoweisiaceae instead of Orthotrichaceae is based on the pres- ence of epigametophytic plants in Amphidium, which are unknown in the Orthotrichaceae, on the rhizoid topography similar to Dicranaceae and different from that in Orthotricha- ceae, the pattern of papillosity of leaf cells, and on recent evidence from nucleotide sequences. Key words: Amphidium, Papua New Guinea, rhizoid topography, systematics, taxonomy, West Irian INTRODUCTION et al. (1999). Our studies are mainly based on the collections of Koponen and Norris from the Huon This paper belongs to a series dealing with the Peninsula, Papua New Guinea (H). Amphidium bryophyte flora of Western Melanesia, which in- tortuosum was collected twice during Koponen- cludes West Irian, Papua New Guinea and the Norris mission and was previously reported there- Solomon Islands.