Validation of Ordinal and Family Names for a Triassic Fossil Liverwort, Naiadita (Naiaditaceae, Marchantiopsida)
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The Origin and Early Evolution of Plants on Land
review article The origin and early evolution of plants on land Paul Kenrick & Peter R. Crane . The origin and early evolution of land plants in the mid-Palaeozoic era, between about 480 and 360 million years ago, was an important event in the history of life, with far-reaching consequences for the evolution of terrestrial organisms and global environments. A recent surge of interest, catalysed by palaeobotanical discoveries and advances in the systematics of living plants, provides a revised perspective on the evolution of early land plants and suggests new directions for future research. The origin and early diversification of land plants marks an interval Eoembryophytic (mid-Ordovician [early Llanvirn: ϳ476 Myr] to of unparalleled innovation in the history of plant life. From a simple Early Silurian [late Llandovery: ϳ432 Myr])3. Spore tetrads (com- plant body consisting of only a few cells, land plants (liverworts, prising four membrane-bound spores; Fig. 2d) appear over a broad hornworts, mosses and vascular plants) evolved an elaborate two- geographic area in the mid-Ordovician and provide the first good phase life cycle and an extraordinary array of complex organs and evidence of land plants3,26,29. The combination of a decay-resistant tissue systems. Specialized sexual organs (gametangia), stems with wall (implying the presence of sporopollenin) and tetrahedral an intricate fluid transport mechanism (vascular tissue), structural configuration (implying haploid meiotic products) is diagnostic tissues (such as wood), epidermal structures for respiratory gas of land plants. The precise relationships of the spore producers exchange (stomates), leaves and roots of various kinds, diverse within land plants are controversial, but evidence of tetrads and spore-bearing organs (sporangia), seeds and the tree habit had all other spore types (such as dyads) in Late Silurian and Devonian evolved by the end of the Devonian period. -
Domenico Puntillo & Michele Puntillo on the Presence of Riella Notarisii
Fl. Medit. 24: 93-97 doi: 10.7320/FlMedit24.093a Revised Version published online on 7 January 2015 Domenico Puntillo & Michele Puntillo On the presence of Riella notarisii (Riellaceae) in the peninsular Italy Abstract Puntillo, D. & Puntillo, M.: On the presence of Riella notarisii (Riellaceae) in the peninsular Italy. — Fl. Medit. 24: 93-97. 2014. — ISSN: 1120-4052 printed, 2240-4538 online. First finding of Riella notarisii (Mont.) Mont. (Hepaticae, Riellaceae) in peninsular Italy; an aquatic liverwort included in the red list of Italian flora. The occurrence in Calabria (South Italy) is reported. Some notes on its ecology, taxonomy and corology are presented. Key words: Hepaticae, Mosses, Flora. Introduction The genus Riella includes some 24 species of thalloid aquatic liverworts distributed worldwide except in Antarctica. The species represented in Europe and Macaronesia are R. helicophylla (Bory & Mont.) Mont., R. notarisii (Mont.) Mont., R. parisii Gott. ex Gott. & Rabenh. and R. cossoniana Trabut (Cirjuano & al. 1988). The only representa- tive of the genus in Italy is R. notarisii recorded only in two localities of Sardinia (Pula and Cagliari) and a little population at the Gulf of Gela, Sicily (Privitera & Puglisi 1997). Riella is a very old genus probably Paleozoic (Shuster 1992) enclosed in the fam- ily Riellaceae (Engler 1892) in the order Spaerocarpales (Heeg 1891). Molecolar data indicate that represents basal and divergent line of Marchantiopsida (Forrest & Crandall-Stotler 2005; He-Nygrén & al. 2006). Nomenclatural notes Historical nomenclature and worldwide distribution of the genus Riella were treated by many autors (Allorge 1932; Persson & Iman 1960; Mueller 1954; Duell 1983). Riella notarisii was described by Montagne as Sphaerocarpus notarisii (Montagne ex de Notaris, 1838). -
Number of Living Species in Australia and the World
Numbers of Living Species in Australia and the World 2nd edition Arthur D. Chapman Australian Biodiversity Information Services australia’s nature Toowoomba, Australia there is more still to be discovered… Report for the Australian Biological Resources Study Canberra, Australia September 2009 CONTENTS Foreword 1 Insecta (insects) 23 Plants 43 Viruses 59 Arachnida Magnoliophyta (flowering plants) 43 Protoctista (mainly Introduction 2 (spiders, scorpions, etc) 26 Gymnosperms (Coniferophyta, Protozoa—others included Executive Summary 6 Pycnogonida (sea spiders) 28 Cycadophyta, Gnetophyta under fungi, algae, Myriapoda and Ginkgophyta) 45 Chromista, etc) 60 Detailed discussion by Group 12 (millipedes, centipedes) 29 Ferns and Allies 46 Chordates 13 Acknowledgements 63 Crustacea (crabs, lobsters, etc) 31 Bryophyta Mammalia (mammals) 13 Onychophora (velvet worms) 32 (mosses, liverworts, hornworts) 47 References 66 Aves (birds) 14 Hexapoda (proturans, springtails) 33 Plant Algae (including green Reptilia (reptiles) 15 Mollusca (molluscs, shellfish) 34 algae, red algae, glaucophytes) 49 Amphibia (frogs, etc) 16 Annelida (segmented worms) 35 Fungi 51 Pisces (fishes including Nematoda Fungi (excluding taxa Chondrichthyes and (nematodes, roundworms) 36 treated under Chromista Osteichthyes) 17 and Protoctista) 51 Acanthocephala Agnatha (hagfish, (thorny-headed worms) 37 Lichen-forming fungi 53 lampreys, slime eels) 18 Platyhelminthes (flat worms) 38 Others 54 Cephalochordata (lancelets) 19 Cnidaria (jellyfish, Prokaryota (Bacteria Tunicata or Urochordata sea anenomes, corals) 39 [Monera] of previous report) 54 (sea squirts, doliolids, salps) 20 Porifera (sponges) 40 Cyanophyta (Cyanobacteria) 55 Invertebrates 21 Other Invertebrates 41 Chromista (including some Hemichordata (hemichordates) 21 species previously included Echinodermata (starfish, under either algae or fungi) 56 sea cucumbers, etc) 22 FOREWORD In Australia and around the world, biodiversity is under huge Harnessing core science and knowledge bases, like and growing pressure. -
Checklist of the Liverworts and Hornworts of the Interior Highlands of North America in Arkansas, Illinois, Missouri and Oklahoma
Checklist of the Liverworts and Hornworts of the Interior Highlands of North America In Arkansas, Illinois, Missouri and Oklahoma Stephen L. Timme T. M. Sperry Herbarium ‐ Biology Pittsburg State University Pittsburg, Kansas 66762 and 3 Bowness Lane Bella Vista, AR 72714 [email protected] Paul Redfearn, Jr. 5238 Downey Ave. Independence, MO 64055 Introduction Since the last publication of a checklist of liverworts and hornworts of the Interior Highlands (1997)), many new county and state records have been reported. To make the checklist useful, it was necessary to update it since its last posting. The map of the Interior Highlands of North America that appears in Redfearn (1983) does not include the very southeast corner of Kansas. However, the Springfield Plateau encompasses some 88 square kilometers of this corner of the state and includes limestone and some sandstone and shale outcrops. The vegetation is typical Ozarkian flora, dominated by oak and hickory. This checklist includes liverworts and hornworts collected from Cherokee County, Kansas. Most of what is known for the area is the result of collections by R. McGregor published in 1955. The majority of his collections are deposited in the herbarium at the New York Botanical Garden (NY). This checklist only includes the region defined as the Interior Highlands of North America. This includes the Springfield Plateau, Salem Plateau, St. Francois Mountains, Boston Mountains, Arkansas Valley, Ouachita Mountains and Ozark Hills. It encompasses much of southern Missouri south of the Missouri River, southwest Illinois; most of Arkansas except the Mississippi Lowlands and the Coastal Plain, the extreme southeastern corner of Kansas, and eastern Oklahoma (Fig. -
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. -
Ordovician Land Plants and Fungi from Douglas Dam, Tennessee
PROOF The Palaeobotanist 68(2019): 1–33 The Palaeobotanist 68(2019): xxx–xxx 0031–0174/2019 0031–0174/2019 Ordovician land plants and fungi from Douglas Dam, Tennessee GREGORY J. RETALLACK Department of Earth Sciences, University of Oregon, Eugene, OR 97403, USA. *Email: gregr@uoregon. edu (Received 09 September, 2019; revised version accepted 15 December, 2019) ABSTRACT The Palaeobotanist 68(1–2): Retallack GJ 2019. Ordovician land plants and fungi from Douglas Dam, Tennessee. The Palaeobotanist 68(1–2): xxx–xxx. 1–33. Ordovician land plants have long been suspected from indirect evidence of fossil spores, plant fragments, carbon isotopic studies, and paleosols, but now can be visualized from plant compressions in a Middle Ordovician (Darriwilian or 460 Ma) sinkhole at Douglas Dam, Tennessee, U. S. A. Five bryophyte clades and two fungal clades are represented: hornwort (Casterlorum crispum, new form genus and species), liverwort (Cestites mirabilis Caster & Brooks), balloonwort (Janegraya sibylla, new form genus and species), peat moss (Dollyphyton boucotii, new form genus and species), harsh moss (Edwardsiphyton ovatum, new form genus and species), endomycorrhiza (Palaeoglomus strotheri, new species) and lichen (Prototaxites honeggeri, new species). The Douglas Dam Lagerstätte is a benchmark assemblage of early plants and fungi on land. Ordovician plant diversity now supports the idea that life on land had increased terrestrial weathering to induce the Great Ordovician Biodiversification Event in the sea and latest Ordovician (Hirnantian) -
Study of a New Population of the Argentinian Endemic Species Riella
cryptogamie Bryologie 2019 ● 40 ● 12 DIRECTEUR DE LA PUBLICATION : Bruno David, Président du Muséum national d’Histoire naturelle RÉDACTEURS EN CHEF / EDITORS-IN-CHIEF : Denis LAMY ASSISTANTS DE RÉDACTION / ASSISTANT EDITORS : Marianne SALAÜN ([email protected]) MISE EN PAGE / PAGE LAYOUT : Marianne SALAÜN RÉDACTEURS ASSOCIÉS / ASSOCIATE EDITORS Biologie moléculaire et phylogénie / Molecular biology and phylogeny Bernard GOFFINET Department of Ecology and Evolutionary Biology, University of Connecticut (United States) Mousses d’Europe / European mosses Isabel DRAPER Centro de Investigación en Biodiversidad y Cambio Global (CIBC-UAM), Universidad Autónoma de Madrid (Spain) Francisco LARA GARCÍA Centro de Investigación en Biodiversidad y Cambio Global (CIBC-UAM), Universidad Autónoma de Madrid (Spain) Mousses d’Afrique et d’Antarctique / African and Antarctic mosses Rysiek OCHYRA Laboratory of Bryology, Institute of Botany, Polish Academy of Sciences, Krakow (Pologne) Bryophytes d’Asie / Asian bryophytes Rui-Liang ZHU School of Life Science, East China Normal University, Shanghai (China) Bioindication / Biomonitoring Franck-Olivier DENAYER Faculté des Sciences Pharmaceutiques et Biologiques de Lille, Laboratoire de Botanique et de Cryptogamie, Lille (France) Écologie des bryophytes / Ecology of bryophyte Nagore GARCÍA MEDINA Department of Biology (Botany), and Centro de Investigación en Biodiversidad y Cambio Global (CIBC-UAM), Universidad Autónoma de Madrid (Spain) COUVERTURE / COVER : Extraits d’éléments de la Figure 2 / Extracts of -
Chapter 3-1 Sexuality: Sexual Strategies Janice M
Glime, J. M. and Bisang, I. 2017. Sexuality: Sexual Strategies. Chapt. 3-1. In: Glime, J. M. Bryophyte Ecology. Volume 1. 3-1-1 Physiological Ecology. Ebook sponsored by Michigan Technological University and the International Association of Bryologists. Last updated 2 April 2017 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology/>. CHAPTER 3-1 SEXUALITY: SEXUAL STRATEGIES JANICE M. GLIME AND IRENE BISANG TABLE OF CONTENTS Expression of Sex............................................................................................................................................... 3-1-2 Unisexual and Bisexual Taxa............................................................................................................................. 3-1-2 Sex Chromosomes....................................................................................................................................... 3-1-6 An unusual Y Chromosome........................................................................................................................ 3-1-7 Gametangial Arrangement.......................................................................................................................... 3-1-8 Origin of Bisexuality in Bryophytes ................................................................................................................ 3-1-11 Monoicy as a Derived/Advanced Character.............................................................................................. 3-1-11 Anthocerotophyta and Multiple Reversals............................................................................................... -
AMBRA1 Controls Plant Development and Senescence in Physcomitrella Patens
Presentation type: Oral Presentation, Poster Presentation (underline the preferred type) AMBRA1 controls plant development and senescence in Physcomitrella patens. Alessandro Alboresi1, Jessica Ceccato1, Tomas Morosinotto1, Luisa Dalla Valle1. The first one should be the presenting/corresponding author (underlined) 1Dipartimento di Biologia, Università di Padova, Via Ugo Bassi 58/B, 35121, Padova ([email protected]; [email protected]; [email protected]) Autophagy is a universal mechanism that in plants control development, resistance to stresses and starvation. The role of autophagy is possible thanks to the programmed degradation of cell material that is delivered to the vacuole where hydrolases and proteases are localized. So far, many autophagy-related proteins (ATGs) have been identified. Some of them are universal, some are either specific to animals, plants or yeast. ATG protein complexes govern autophagosome initiation, nucleation, expansion, and maturation. In particular, the regulation of nucleation by the ATG6 (Beclin-1 in mammals) complex has not been well defined in plants. Here we described the study of the Activating Molecule in Beclin 1-Regulated Autophagy (AMBRA1) protein, recently identified in mice and then characterized in our department in zebrafish and in the non-vertebrate chordate Botryllus schlosseri. In animals AMBRA1 is a positive regulator of autophagy that binds Beclin-1 upon autophagic stimuli. AMBRA1 is a large intrinsically disordered protein, able to bind other regulatory partners involved in cell processes such as autophagy, apoptosis, cell proliferation, development and cancer. AMBRA1 sequence was found in plant genomes and we are studying its function in Physcomitrella patens where two lowly expressed genes are present, AMBRA1a and AMBRA1b. -
Divergence Times and the Evolution of Morphological Complexity in an Early Land Plant Lineage (Marchantiopsida) with a Slow Molecular Rate
Research Divergence times and the evolution of morphological complexity in an early land plant lineage (Marchantiopsida) with a slow molecular rate Juan Carlos Villarreal A.1,3,4, Barbara J. Crandall-Stotler2, Michelle L. Hart1, David G. Long1 and Laura L. Forrest1 1Royal Botanic Gardens Edinburgh, 20A Inverleith Row, Edinburgh, EH3 5LR, UK; 2Department of Plant Biology, Southern Illinois University, Carbondale, IL 62901, USA; 3Present address: Smithsonian Tropical Research Institute, Ancon, 0843-03092 Panama, Republic of Panama; 4Present address: Departement de Biologie, Universite Laval, Quebec, Canada G1V 0A6 Summary Authors for correspondence: We present a complete generic-level phylogeny of the complex thalloid liverworts, a lineage Juan Carlos Villarreal A that includes the model system Marchantia polymorpha. The complex thalloids are remark- Tel: +1418 656 3180 able for their slow rate of molecular evolution and for being the only extant plant lineage to Email: [email protected] differentiate gas exchange tissues in the gametophyte generation. We estimated the diver- Laura L. Forrest gence times and analyzed the evolutionary trends of morphological traits, including air cham- Tel: + 44(0) 131248 2952 bers, rhizoids and specialized reproductive structures. Email: [email protected] A multilocus dataset was analyzed using maximum likelihood and Bayesian approaches. Received: 29 June 2015 Relative rates were estimated using local clocks. Accepted: 15 September 2015 Our phylogeny cements the early branching in complex thalloids. Marchantia is supported in one of the earliest divergent lineages. The rate of evolution in organellar loci is slower than New Phytologist (2015) for other liverwort lineages, except for two annual lineages. -
The Genus Plagiochasma (Aytoniaceae, Marchantiopsida) in Thailand
Cryptogamie, Bryologie, 2014, 35 (2): 127-132 © 2014 Adac. Tous droits réservés The genus Plagiochasma (Aytoniaceae, Marchantiopsida) in Thailand Sahut CHANTANAORRAPINT* & Kitichate SRIDITH Department of Biology, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla, 90112 Thailand Abstract – The genus Plagiochasma Lehm. et Lindenb. in Thailand is reviewed, based on herbarium specimens and especially on recently collections. The genus is reported for the first time from Thailand. Two species are recognized, namely P. appendiculatum Lehm. et Lindenb. and P. cordatum Lehm. et Lindenb. Descriptions, illustrations, and a key to species are provided. Aytoniaceae / complex thalloid liverworts / Marchantiopsida / Plagiochasma / Thailand INTRODUCTION Thailand is well-known as one of the richest areas in term of biodiversity. This area is located in both the Indo-Burmese and Sundaland hotspots (Myers et al., 2000), and includes areas identified as the overlapping zone of the Sino- Himalayan and Malesian floristic regions (Smitinand, 1989). The first report for liverworts in Thailand was made by Stephani (1902) who recorded seventeen species of liverworts from Koh Chang (Island), including four new species. During 1901-1904, Hosseus collected plant specimens from the northern part of the country, and reported five liverworts (Hosseus, 1911). Later, many contributions of Thai liverworts were received. In 2008, Lai et al. published an updated checklist of Thai liverworts and hornworts based on the literatures and their currently collections, including 376 species of liverworts. In recent years, some additions of interesting liverworts to Thailand have been reported (Kornochalert et al., 2010; He et al. 2012, 2013; Kornochalert et al., 2012; Wei & Zhu 2013; Sukkharak, 2013). -
Wikstrom2009chap13.Pdf
Liverworts (Marchantiophyta) Niklas Wikströma,*, Xiaolan He-Nygrénb, and our understanding of phylogenetic relationships among A. Jonathan Shawc major lineages and the origin and divergence times of aDepartment of Systematic Botany, Evolutionary Biology Centre, those lineages. Norbyvägen 18D, Uppsala University, Norbyvägen 18D 75236, Altogether, liverworts (Phylum Marchantiophyta) b Uppsala, Sweden; Botanical Museum, Finnish Museum of Natural comprise an estimated 5000–8000 living species (8, 9). History, University of Helsinki, P.O. Box 7, 00014 Helsinki, Finland; Early and alternative classiA cations for these taxa have cDepartment of Biology, Duke University, Durham, NC 27708, USA *To whom correspondence should be addressed (niklas.wikstrom@ been numerous [reviewed by Schuster ( 10)], but the ebc.uu.se) arrangement of terminal taxa (species, genera) into lar- ger groups (e.g., families and orders) based on morpho- logical criteria alone began in the 1960s and 1970s with Abstract the work of Schuster (8, 10, 11) and Schljakov (12, 13), and culminated by the turn of the millenium with the work Liverworts (Phylum Marchantiophyta) include 5000–8000 of Crandall-Stotler and Stotler (14). 7 ree morphological species. Phylogenetic analyses divide liverworts into types of plant bodies (gametophytes) have generally been Haplomitriopsida, Marchantiopsida, and Jungerman- recognized and used in liverwort classiA cations: “com- niopsida. Complex thalloids are grouped with Blasiales in plex thalloids” including ~6% of extant species diversity Marchantiopsida, and leafy liverworts are grouped with and with a thalloid gametophyte that is organized into Metzgeriidae and Pelliidae in Jungermanniopsida. The distinct layers; “leafy liverworts”, by far the most speci- timetree shows an early Devonian (408 million years ago, ose group, including ~86% of extant species diversity and Ma) origin for extant liverworts.