Class Haplomitriopsida In

Total Page:16

File Type:pdf, Size:1020Kb

Class Haplomitriopsida In Citation: Url1. https://blogs.ubc.ca/biology“Introduction to Bryophytes” SYSTEMATICS OF DIVISION MARCHANTIOPHYTA (HAPLOMITRIOPSIDA, MARCHANTIOPSIDA AND JUNGERMANNIOPSIDA) Class Haplomitriopsida In the class Haplomitriopsida the plants are acrocarpous and the gametophyte is leafy. Generally the stems are able to secrete copious amounts of mucilage, which is discharged from the epidermal cells. The gametangia are typically situated in the axils of the leaves or lobules. It is worth noting however that the archegonia and antheridia are normally not differentiated from the surrounding tissue of the gametophyte. The sporophytes, which are relatively large, generally open along four lines of dehiscence. Subclass Haplomitriidae The species in the subclass Haplomitriidae have leaves that are 3-ranked on the stem. A closer look will reveal the presence of two rows of lateral leaves and one row of underleaves, the latter being reduced. Oil bodies, which are small, can be found within the leaf cells of these species. Although the plants within this subclass lack rhizoids they have an extensive rhizomatous network. Species in Haplomitriidae can either be diocious or monoicous and the female reproductive structures may be either acrogynous or anacrogynous. Althought the perianth is lacking, the female protective tissue surrounding the developing sporangium may be a shoot- calyptra or a true calyptra. The sporophyte, which is typically cylindrical in shape and robust, has a sporangial jacket that is unistratose. A closer look at the sporangial wall will reveal that each cell has a single transverse band thickening. Spore dispersal in this subclass generally occurs along 1, 2, or 4 lines of dehiscence. Class Jungermanniopsida Class Jungermanniopsida includes leafy and simple thalloid liverworts. There is a lack of shared characteristics between these two groups. The leaves of leafy liverworts may be entire or lobed with various forms of insertion. The thalloid liverworts may be branched. Oil bodies may or may not be present. When present, oil bodies are typically found in both gametophytic and sporophytic regions of the liverwort. There are multiple oil bodies per cell. REFERENCES 1. Url1. https://blogs.ubc.ca/biology“Introduction to Bryophytes”.
Recommended publications
  • Identifikasi Keanekaragaman Marchantiophyta Di Kawasan Air Terjun Parangkikis Pagerwojo Tulungagung
    Jurnal Biologi dan Pembelajarannya, Vol 6 No 2, Oktober 2019. Pp: 17-21 e-ISSN: 2406 – 8659 IDENTIFIKASI KEANEKARAGAMAN MARCHANTIOPHYTA DI KAWASAN AIR TERJUN PARANGKIKIS PAGERWOJO TULUNGAGUNG Repik Febriansah, Eni Setyowati*), Arbaul Fauziah Jurusan Tadris Biologi, Fakultas Tarbiyah dan Ilmu Keguruan, IAIN Tulungagung Jalan Mayor Sujadi No. 46 Tulungagung *)Email: [email protected] Abstrak Penelitian ini bertujuan untuk mengkaji keanekaragaman jenis dari Divisi Marchantiophyta di Kawasan Air Terjun Parangkikis. Pengambilan sampel dilakukan pada bulan Desember 2018 hingga Maret 2019 dengan metode jelajah di sekitar Air Terjun Parangkikis Pagerwojo, Tulungagung. Identifikasi Marchantiophyta dilakukan di Laboratorium IPA Fakultas Tarbiyah dan Ilmu Keguruan IAIN Tulungagung. Hasil penelitian menunjukkan bahwa di kawasan Air Terjun Parangkikis terdapat dua kelas, yaitu Marchantiopsida dan Jungermanniopsida. Pada kelas Marchantiopsida hanya terdapat satu ordo, yaitu Marchantiales. Sedangkan pada kelas Jungermanniopsida meliputi tiga ordo yaitu Jungermanniales, Porellales, dan Pallviciniales. Kata kunci- Air Terjun Parangkikis, Keanekaragaman, Marchantiophyta PENDAHULUAN Tumbuhan lumut merupakan salah satu tumbuhan yang memiliki keanekaragaman cukup tinggi. Lumut merupakan kelompok tumbuhan yang berukuran kecil yang tempat tumbuhnya menempel pada berbagai substrat seperti pohon, serasah, kayu mati, kayu lapuk, tanah, maupun bebatuan. Lumut dapat tumbuh pada lingkungan lembab dengan penyinaran yang cukup [1]. Secara ekologis lumut berperan penting di dalam fungsi ekosistem. Tumbuhan lumut dapat digunakan sebagai bioindikator lingkungan yang menentukan lingkungan tersebut masih terjaga dengan baik atau sudah tereksploitasi [2]. Lumut hati dapat berfungsi sebagai bioakumulator logam berat [3] dan inhibitor pertumbuhan protozoa [4]. Air Terjun Parangkikis merupakan salah satu daerah pegunungan di Desa Gambiran Kecamatan Pagerwojo Kabupaten Tulungagung yang kaya dengan berbagai jenis lumut. Namun, penelitian tumbuhan lumut di kawasan tersebut belum banyak dilakukan.
    [Show full text]
  • 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.
    [Show full text]
  • Seed Plant Models
    Review Tansley insight Why we need more non-seed plant models Author for correspondence: Stefan A. Rensing1,2 Stefan A. Rensing 1 2 Tel: +49 6421 28 21940 Faculty of Biology, University of Marburg, Karl-von-Frisch-Str. 8, 35043 Marburg, Germany; BIOSS Biological Signalling Studies, Email: stefan.rensing@biologie. University of Freiburg, Sch€anzlestraße 18, 79104 Freiburg, Germany uni-marburg.de Received: 30 October 2016 Accepted: 18 December 2016 Contents Summary 1 V. What do we need? 4 I. Introduction 1 VI. Conclusions 5 II. Evo-devo: inference of how plants evolved 2 Acknowledgements 5 III. We need more diversity 2 References 5 IV. Genomes are necessary, but not sufficient 3 Summary New Phytologist (2017) Out of a hundred sequenced and published land plant genomes, four are not of flowering plants. doi: 10.1111/nph.14464 This severely skewed taxonomic sampling hinders our comprehension of land plant evolution at large. Moreover, most genetically accessible model species are flowering plants as well. If we are Key words: Charophyta, evolution, fern, to gain a deeper understanding of how plants evolved and still evolve, and which of their hornwort, liverwort, moss, Streptophyta. developmental patterns are ancestral or derived, we need to study a more diverse set of plants. Here, I thus argue that we need to sequence genomes of so far neglected lineages, and that we need to develop more non-seed plant model species. revealed much, the exact branching order and evolution of the I. Introduction nonbilaterian lineages is still disputed (Lanna, 2015). Research on animals has for a long time relied on a number of The first (small) plant genome to be sequenced was of THE traditional model organisms, such as mouse, fruit fly, zebrafish or model plant, the weed Arabidopsis thaliana (c.
    [Show full text]
  • 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.
    [Show full text]
  • Plant Life Magill’S 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.
    [Show full text]
  • Introduction to Botany. Lecture 31
    Questions and answers Kingdom Vegetabilia: plants Introduction to Botany. Lecture 31 Alexey Shipunov Minot State University November 16, 2011 Shipunov BIOL 154.31 Questions and answers Kingdom Vegetabilia: plants Outline 1 Questions and answers 2 Kingdom Vegetabilia: plants Bryophyta: mosses Shipunov BIOL 154.31 Questions and answers Kingdom Vegetabilia: plants Outline 1 Questions and answers 2 Kingdom Vegetabilia: plants Bryophyta: mosses Shipunov BIOL 154.31 2 Questions and answers Kingdom Vegetabilia: plants Previous final question: the answer 1 Arabidopsis thaliana (L.) Heynh 2 Citrus 3 Piperaceae Where is a genus name? Shipunov BIOL 154.31 Questions and answers Kingdom Vegetabilia: plants Previous final question: the answer 1 Arabidopsis thaliana (L.) Heynh 2 Citrus 3 Piperaceae Where is a genus name? 2 Shipunov BIOL 154.31 Questions and answers Kingdom Vegetabilia: plants Results of Exam 3 (statistical summary) Summary: Min. 1st Qu. Median Mean 3rd Qu. Max. NA’s 43.00 67.00 79.00 78.36 92.00 108.00 5.00 Grades: F D C B max 61 72 82 92 102 Shipunov BIOL 154.31 Questions and answers Kingdom Vegetabilia: plants Results of Exam 3 (the curve) Density estimation for Exam 3 (Biol 154) 61 92 (F) (B) Points Shipunov BIOL 154.31 Questions and answers Bryophyta: mosses Kingdom Vegetabilia: plants Kingdom Vegetabilia: plants Bryophyta: mosses Shipunov BIOL 154.31 Questions and answers Bryophyta: mosses Kingdom Vegetabilia: plants Three main phyla Bryophyta: gametophyte predominance Pteridophyta: sporophyte predominance, no seed Spermatophyta:
    [Show full text]
  • Aquatic and Wet Marchantiophyta, Order Metzgeriales: Aneuraceae
    Glime, J. M. 2021. Aquatic and Wet Marchantiophyta, Order Metzgeriales: Aneuraceae. Chapt. 1-11. In: Glime, J. M. Bryophyte 1-11-1 Ecology. Volume 4. Habitat and Role. Ebook sponsored by Michigan Technological University and the International Association of Bryologists. Last updated 11 April 2021 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology/>. CHAPTER 1-11: AQUATIC AND WET MARCHANTIOPHYTA, ORDER METZGERIALES: ANEURACEAE TABLE OF CONTENTS SUBCLASS METZGERIIDAE ........................................................................................................................................... 1-11-2 Order Metzgeriales............................................................................................................................................................... 1-11-2 Aneuraceae ................................................................................................................................................................... 1-11-2 Aneura .......................................................................................................................................................................... 1-11-2 Aneura maxima ............................................................................................................................................................ 1-11-2 Aneura mirabilis .......................................................................................................................................................... 1-11-7 Aneura pinguis ..........................................................................................................................................................
    [Show full text]
  • S41467-021-25308-W.Pdf
    ARTICLE https://doi.org/10.1038/s41467-021-25308-w OPEN Phylogenomics of a new fungal phylum reveals multiple waves of reductive evolution across Holomycota ✉ ✉ Luis Javier Galindo 1 , Purificación López-García 1, Guifré Torruella1, Sergey Karpov2,3 & David Moreira 1 Compared to multicellular fungi and unicellular yeasts, unicellular fungi with free-living fla- gellated stages (zoospores) remain poorly known and their phylogenetic position is often 1234567890():,; unresolved. Recently, rRNA gene phylogenetic analyses of two atypical parasitic fungi with amoeboid zoospores and long kinetosomes, the sanchytrids Amoeboradix gromovi and San- chytrium tribonematis, showed that they formed a monophyletic group without close affinity with known fungal clades. Here, we sequence single-cell genomes for both species to assess their phylogenetic position and evolution. Phylogenomic analyses using different protein datasets and a comprehensive taxon sampling result in an almost fully-resolved fungal tree, with Chytridiomycota as sister to all other fungi, and sanchytrids forming a well-supported, fast-evolving clade sister to Blastocladiomycota. Comparative genomic analyses across fungi and their allies (Holomycota) reveal an atypically reduced metabolic repertoire for sanchy- trids. We infer three main independent flagellum losses from the distribution of over 60 flagellum-specific proteins across Holomycota. Based on sanchytrids’ phylogenetic position and unique traits, we propose the designation of a novel phylum, Sanchytriomycota. In addition, our results indicate that most of the hyphal morphogenesis gene repertoire of multicellular fungi had already evolved in early holomycotan lineages. 1 Ecologie Systématique Evolution, CNRS, Université Paris-Saclay, AgroParisTech, Orsay, France. 2 Zoological Institute, Russian Academy of Sciences, St. ✉ Petersburg, Russia. 3 St.
    [Show full text]
  • Pteridophyte Fungal Associations: Current Knowledge and Future Perspectives
    This is a repository copy of Pteridophyte fungal associations: Current knowledge and future perspectives. White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/109975/ Version: Accepted Version Article: Pressel, S, Bidartondo, MI, Field, KJ orcid.org/0000-0002-5196-2360 et al. (2 more authors) (2016) Pteridophyte fungal associations: Current knowledge and future perspectives. Journal of Systematics and Evolution, 54 (6). pp. 666-678. ISSN 1674-4918 https://doi.org/10.1111/jse.12227 © 2016 Institute of Botany, Chinese Academy of Sciences. This is the peer reviewed version of the following article: Pressel, S., Bidartondo, M. I., Field, K. J., Rimington, W. R. and Duckett, J. G. (2016), Pteridophyte fungal associations: Current knowledge and future perspectives. Jnl of Sytematics Evolution, 54: 666–678., which has been published in final form at https://doi.org/10.1111/jse.12227. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving. Reuse Unless indicated otherwise, fulltext items are protected by copyright with all rights reserved. The copyright exception in section 29 of the Copyright, Designs and Patents Act 1988 allows the making of a single copy solely for the purpose of non-commercial research or private study within the limits of fair dealing. The publisher or other rights-holder may allow further reproduction and re-use of this version - refer to the White Rose Research Online record for this item. Where records identify the publisher as the copyright holder, users can verify any specific terms of use on the publisher’s website.
    [Show full text]
  • 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...............................................................................................
    [Show full text]
  • Evolution and Networks in Ancient and Widespread Symbioses Between Mucoromycotina and Liverworts
    This is a repository copy of Evolution and networks in ancient and widespread symbioses between Mucoromycotina and liverworts. White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/150867/ Version: Published Version Article: Rimington, WR, Pressel, S, Duckett, JG et al. (2 more authors) (2019) Evolution and networks in ancient and widespread symbioses between Mucoromycotina and liverworts. Mycorrhiza, 29 (6). pp. 551-565. ISSN 0940-6360 https://doi.org/10.1007/s00572-019-00918-x Reuse This article is distributed under the terms of the Creative Commons Attribution (CC BY) licence. This licence allows you to distribute, remix, tweak, and build upon the work, even commercially, as long as you credit the authors for the original work. More information and the full terms of the licence here: https://creativecommons.org/licenses/ Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ Mycorrhiza (2019) 29:551–565 https://doi.org/10.1007/s00572-019-00918-x ORIGINAL ARTICLE Evolution and networks in ancient and widespread symbioses between Mucoromycotina and liverworts William R. Rimington1,2,3 & Silvia Pressel2 & Jeffrey G. Duckett2 & Katie J. Field4 & Martin I. Bidartondo1,3 Received: 29 May 2019 /Accepted: 13 September 2019 /Published online: 13 November 2019 # The Author(s) 2019 Abstract Like the majority of land plants, liverworts regularly form intimate symbioses with arbuscular mycorrhizal fungi (Glomeromycotina).
    [Show full text]
  • 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.
    [Show full text]