Platyhelminthes, Gastrotricha OEB 51 Lab 6: Platyhelminthes, Gastrotricha
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Gastrotricha, Chaetonotida) from Obodska Cave (Montenegro) Based on Morphological and Molecular Characters
European Journal of Taxonomy 354: 1–30 ISSN 2118-9773 https://doi.org/10.5852/ejt.2017.354 www.europeanjournaloftaxonomy.eu 2017 · Kolicka M. et al. This work is licensed under a Creative Commons Attribution 3.0 License. Research article urn:lsid:zoobank.org:pub:51C2BE54-B99B-4464-8FC1-28A5CC6B9586 A new species of freshwater Chaetonotidae (Gastrotricha, Chaetonotida) from Obodska Cave (Montenegro) based on morphological and molecular characters Małgorzata KOLICKA 1,*, Piotr GADAWSKI 2 & Miroslawa DABERT 3 1 Department of Animal Taxonomy and Ecology, Institute of Environmental Biology, Adam Mickiewicz University Poznan, Umultowska 89, 61–614 Poznan, Poland. 2 Department of Invertebrate Zoology and Hydrobiology, University of Łódź, Banacha 12/16, 90–237 Łódź, Poland. 3 Molecular Biology Techniques Laboratory, Faculty of Biology, Adam Mickiewicz University Poznan, Umultowska 89, 61–614 Poznan, Poland. * Corresponding author: [email protected] 2 E-mail: [email protected] 3 E-mail: [email protected] 1 urn:lsid:zoobank.org:author:550BCAA1-FB2B-47CC-A657-0340113C2D83 2 urn:lsid:zoobank.org:author:BCA3F37A-28BD-484C-A3B3-C2169D695A82 3 urn:lsid:zoobank.org:author:8F04FE81-3BC7-44C5-AFAB-6236607130F9 Abstract. Gastrotricha is a cosmopolitan phylum of aquatic and semi-aquatic invertebrates that comprises about 820 described species. Current knowledge regarding freshwater gastrotrichs inhabiting caves is extremely poor and there are no extant data regarding Gastrotricha from Montenegro. We describe a new species from Obodska Cave, which is also the fi rst record of a gastrotrich from this region. Due to its unusual habitat and morphological characteristics, this species may be important when considering the evolution and dispersion routes of Chaetonotidae Gosse, 1864 (sensu Leasi & Todaro 2008). -
Animal Phylogeny and the Ancestry of Bilaterians: Inferences from Morphology and 18S Rdna Gene Sequences
EVOLUTION & DEVELOPMENT 3:3, 170–205 (2001) Animal phylogeny and the ancestry of bilaterians: inferences from morphology and 18S rDNA gene sequences Kevin J. Peterson and Douglas J. Eernisse* Department of Biological Sciences, Dartmouth College, Hanover NH 03755, USA; and *Department of Biological Science, California State University, Fullerton CA 92834-6850, USA *Author for correspondence (email: [email protected]) SUMMARY Insight into the origin and early evolution of the and protostomes, with ctenophores the bilaterian sister- animal phyla requires an understanding of how animal group, whereas 18S rDNA suggests that the root is within the groups are related to one another. Thus, we set out to explore Lophotrochozoa with acoel flatworms and gnathostomulids animal phylogeny by analyzing with maximum parsimony 138 as basal bilaterians, and with cnidarians the bilaterian sister- morphological characters from 40 metazoan groups, and 304 group. We suggest that this basal position of acoels and gna- 18S rDNA sequences, both separately and together. Both thostomulids is artifactal because for 1000 replicate phyloge- types of data agree that arthropods are not closely related to netic analyses with one random sequence as outgroup, the annelids: the former group with nematodes and other molting majority root with an acoel flatworm or gnathostomulid as the animals (Ecdysozoa), and the latter group with molluscs and basal ingroup lineage. When these problematic taxa are elim- other taxa with spiral cleavage. Furthermore, neither brachi- inated from the matrix, the combined analysis suggests that opods nor chaetognaths group with deuterostomes; brachiopods the root lies between the deuterostomes and protostomes, are allied with the molluscs and annelids (Lophotrochozoa), and Ctenophora is the bilaterian sister-group. -
Describing Species
DESCRIBING SPECIES Practical Taxonomic Procedure for Biologists Judith E. Winston COLUMBIA UNIVERSITY PRESS NEW YORK Columbia University Press Publishers Since 1893 New York Chichester, West Sussex Copyright © 1999 Columbia University Press All rights reserved Library of Congress Cataloging-in-Publication Data © Winston, Judith E. Describing species : practical taxonomic procedure for biologists / Judith E. Winston, p. cm. Includes bibliographical references and index. ISBN 0-231-06824-7 (alk. paper)—0-231-06825-5 (pbk.: alk. paper) 1. Biology—Classification. 2. Species. I. Title. QH83.W57 1999 570'.1'2—dc21 99-14019 Casebound editions of Columbia University Press books are printed on permanent and durable acid-free paper. Printed in the United States of America c 10 98765432 p 10 98765432 The Far Side by Gary Larson "I'm one of those species they describe as 'awkward on land." Gary Larson cartoon celebrates species description, an important and still unfinished aspect of taxonomy. THE FAR SIDE © 1988 FARWORKS, INC. Used by permission. All rights reserved. Universal Press Syndicate DESCRIBING SPECIES For my daughter, Eliza, who has grown up (andput up) with this book Contents List of Illustrations xiii List of Tables xvii Preface xix Part One: Introduction 1 CHAPTER 1. INTRODUCTION 3 Describing the Living World 3 Why Is Species Description Necessary? 4 How New Species Are Described 8 Scope and Organization of This Book 12 The Pleasures of Systematics 14 Sources CHAPTER 2. BIOLOGICAL NOMENCLATURE 19 Humans as Taxonomists 19 Biological Nomenclature 21 Folk Taxonomy 23 Binomial Nomenclature 25 Development of Codes of Nomenclature 26 The Current Codes of Nomenclature 50 Future of the Codes 36 Sources 39 Part Two: Recognizing Species 41 CHAPTER 3. -
Atp8 Is in the Ground Pattern of Flatworm Mitochondrial Genomes Bernhard Egger1* , Lutz Bachmann2 and Bastian Fromm3
Egger et al. BMC Genomics (2017) 18:414 DOI 10.1186/s12864-017-3807-2 RESEARCH ARTICLE Open Access Atp8 is in the ground pattern of flatworm mitochondrial genomes Bernhard Egger1* , Lutz Bachmann2 and Bastian Fromm3 Abstract Background: To date, mitochondrial genomes of more than one hundred flatworms (Platyhelminthes) have been sequenced. They show a high degree of similarity and a strong taxonomic bias towards parasitic lineages. The mitochondrial gene atp8 has not been confidently annotated in any flatworm sequenced to date. However, sampling of free-living flatworm lineages is incomplete. We addressed this by sequencing the mitochondrial genomes of the two small-bodied (about 1 mm in length) free-living flatworms Stenostomum sthenum and Macrostomum lignano as the first representatives of the earliest branching flatworm taxa Catenulida and Macrostomorpha respectively. Results: We have used high-throughput DNA and RNA sequence data and PCR to establish the mitochondrial genome sequences and gene orders of S. sthenum and M. lignano. The mitochondrial genome of S. sthenum is 16,944 bp long and includes a 1,884 bp long inverted repeat region containing the complete sequences of nad3, rrnS, and nine tRNA genes. The model flatworm M. lignano has the smallest known mitochondrial genome among free- living flatworms, with a length of 14,193 bp. The mitochondrial genome of M. lignano lacks duplicated genes, however, tandem repeats were detected in a non-coding region. Mitochondrial gene order is poorly conserved in flatworms, only a single pair of adjacent ribosomal or protein-coding genes – nad4l-nad4 – was found in S. sthenum and M. -
Gastrotricha of Sweden – Biodiversity and Phylogeny
Gastrotricha of Sweden – Biodiversity and Phylogeny Tobias Kånneby Department of Zoology Stockholm University 2011 Gastrotricha of Sweden – Biodiversity and Phylogeny Doctoral dissertation 2011 Tobias Kånneby Department of Zoology Stockholm University SE-106 91 Stockholm Sweden Department of Invertebrate Zoology Swedish Museum of Natural History PO Box 50007 SE-104 05 Stockholm Sweden [email protected] [email protected] ©Tobias Kånneby, Stockholm 2011 ISBN 978-91-7447-397-1 Cover Illustration: Therése Pettersson Printed in Sweden by US-AB, Stockholm 2011 Distributor: Department of Zoology, Stockholm University Till Mamma och Pappa ABSTRACT Gastrotricha are small aquatic invertebrates with approximately 770 known species. The group has a cosmopolitan distribution and is currently classified into two orders, Chaetonotida and Macrodasyida. The gastrotrich fauna of Sweden is poorly known: a couple of years ago only 29 species had been reported. In Paper I, III, and IV, 5 freshwater species new to science are described. In total 56 species have been recorded for the first time in Sweden during the course of this thesis. Common species with a cosmopolitan distribution, e. g. Chaetonotus hystrix and Lepidodermella squamata, as well as rarer species, e. g. Haltidytes crassus, Ichthydium diacanthum and Stylochaeta scirtetica, are reported. In Paper II molecular data is used to infer phylogenetic relationships within the morphologically very diverse marine family Thaumastodermatidae (Macrodasyida). Results give high support for monophyly of Thaumastodermatidae and also the subfamilies Diplodasyinae and Thaumastoder- matinae. In Paper III the hypothesis of cryptic speciation is tested in widely distributed freshwater gastrotrichs. Heterolepidoderma ocellatum f. sphagnophilum is raised to species under the name H. -
Gastrotricha
Chapter 7 Gastrotricha David L. Strayer, William D. Hummon Rick Hochberg Cary Institute of Ecosystem Studies, Department of Biological Sciences, Ohio Department of Biological Sciences, Millbrook, New York University, Athens, Ohio University of Massachusetts, Lowell, Massachusetts believe that they are most closely related to nematodes, I. Introduction kinorhynchs, loriciferans, nematomorphs, and priaulids II. Anatomy and physiology (i.e., Cycloneuralia[73]), while others[18,27] think that A. External Morphology gastrotrichs are more closely related to rotifers and gnatho- B. Organ System Function stomulids (i.e., Gnathifera[94]) and less closely to turbel- III. Ecology and evolution larians. The gastrotrichs do not fit well into either of these A. Diversity and Distribution schemes. Important general references on gastrotrichs B. Reproduction and Life History include Remane[82], Hyman[50], Voigt[103], d’Hondt[33], C. Ecological Interactions Hummon[44], Ruppert[89,90], Schwank[95], Kisielewski[58,60], D. Evolutionary Relationships and Balsamo and Todaro[5]. The phylum contains two IV. Collecting, rearing, and preparation for orders: Macrodasyida, which consists almost entirely of identification marine species, and Chaetonotida, containing marine, fresh- V. Taxonomic key to Gastrotricha water, and semiterrestrial species. Unless noted otherwise, VI. Selected References the information in this chapter refers to freshwater members of Chaetonotida. Macrodasyidans usually are distinguished from cha- etonotidans by the presence of pharyngeal pores and I. INTRODUCTION more than two pairs of adhesive tubules (Fig. 7.1). Macrodasyidans are common in marine and estuarine Gastrotrichs are among the most abundant and poorly known sands but are barely represented in freshwaters. Two spe- of the freshwater invertebrates. They are nearly ubiquitous cies of freshwater gastrotrichs have been placed in the in the benthos and periphyton of freshwater habitats, with Macrodasyida. -
Musculature of the Primitive Gastrotrich Neodasys (Chaetonotida): Functional Adaptations to the Interstitial Environment and Phylogenetic Significance
Marine Biology (2005) 146: 315–323 DOI 10.1007/s00227-004-1437-0 RESEARCH ARTICLE R. Hochberg Musculature of the primitive gastrotrich Neodasys (Chaetonotida): functional adaptations to the interstitial environment and phylogenetic significance Received: 4 February 2004 / Accepted: 9 July 2004 / Published online: 4 August 2004 Ó Springer-Verlag 2004 Abstract Gastrotrichs are acoelomate micrometazoans Introduction common to marine interstitial environments of sub- littoral sediments and exposed sandy beaches. The Gastrotrichs of the genus Neodasys are microscopic genus Neodasys (Chaetonotida) contains three marine (400–600 lm long) and slender worms that inhabit the species known from oceans and seas worldwide, and pore spaces of fine- and medium-grained coastal marine figures prominently in discussions of gastrotrich ori- sediments worldwide. The slender body form and mul- gins. To gain insight into the phylogenetic position of tiple adhesive organs equips these interstitial worms for Neodasys and to understand the adaptive significance littoral regions with various degrees of water flow, of muscle anatomy in marine interstitial gastrotrichs, a including both low- and high-energy beaches. On sandy, fluorescent phalloidin-linked marker was used to view exposed beaches, wave impact and surge produce pul- the organization of muscles in two species from North satile, high laminar flows that percolate through the America and Australia. Muscular topography of Neo- porous substrate and create ‘‘stormy interstices’’ (Riedl dasys cirritus from Florida, USA, and Neodasys cf. 1971). While little is known of the effects of these uchidai from Queensland, Australia, was found to be interstitial laminar flows on animal behavior (Crenshaw similar between species and to basal species of Mac- 1980), the morphology of the various species that rodasyida; muscles were present in circular, longitudi- inhabit the interstitial realm are recognized to display a nal and helicoidal patterns. -
Comparative Anatomy and Evolution of the Gastrotrich Muscular System
University of New Hampshire University of New Hampshire Scholars' Repository Doctoral Dissertations Student Scholarship Spring 2002 Comparative anatomy and evolution of the gastrotrich muscular system Richard Hochberg University of New Hampshire, Durham Follow this and additional works at: https://scholars.unh.edu/dissertation Recommended Citation Hochberg, Richard, "Comparative anatomy and evolution of the gastrotrich muscular system" (2002). Doctoral Dissertations. 67. https://scholars.unh.edu/dissertation/67 This Dissertation is brought to you for free and open access by the Student Scholarship at University of New Hampshire Scholars' Repository. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of University of New Hampshire Scholars' Repository. For more information, please contact [email protected]. INFORMATION TO USERS This manuscript has been reproduced from the microfilm master. UMI films the text directly from the original or copy submitted. Thus, some thesis and dissertation copies are in typewriter face, while others may be from any type of computer printer. The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleedthrough, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send UMI a complete manuscript and there are missing pages, these will be noted. Also, if unauthorized copyright material had to be removed, a note will indicate the deletion. Oversize materials (e.g., maps, drawings, charts) are reproduced by sectioning the original, beginning at the upper left-hand comer and continuing from left to right in equal sections with small overlaps. -
Ostrovsky Et 2016-Biological R
Matrotrophy and placentation in invertebrates: a new paradigm Andrew Ostrovsky, Scott Lidgard, Dennis Gordon, Thomas Schwaha, Grigory Genikhovich, Alexander Ereskovsky To cite this version: Andrew Ostrovsky, Scott Lidgard, Dennis Gordon, Thomas Schwaha, Grigory Genikhovich, et al.. Matrotrophy and placentation in invertebrates: a new paradigm. Biological Reviews, Wiley, 2016, 91 (3), pp.673-711. 10.1111/brv.12189. hal-01456323 HAL Id: hal-01456323 https://hal.archives-ouvertes.fr/hal-01456323 Submitted on 4 Feb 2017 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Biol. Rev. (2016), 91, pp. 673–711. 673 doi: 10.1111/brv.12189 Matrotrophy and placentation in invertebrates: a new paradigm Andrew N. Ostrovsky1,2,∗, Scott Lidgard3, Dennis P. Gordon4, Thomas Schwaha5, Grigory Genikhovich6 and Alexander V. Ereskovsky7,8 1Department of Invertebrate Zoology, Faculty of Biology, Saint Petersburg State University, Universitetskaja nab. 7/9, 199034, Saint Petersburg, Russia 2Department of Palaeontology, Faculty of Earth Sciences, Geography and Astronomy, Geozentrum, -
Ecology of Old Woman Creek, Ohio
Shagbark hickory (Carya ovata) on a bluff overlooking Old Woman Creek estuary (Charles E. Herdendorf). CHAPTER 1. INTRODUCTION CHAPTER 6. BIOLOGY NON-VASCULAR PLANTS The algal flora and lower plants found in the vicinity of the Research Reserve embrace four of the The non-vascular plants of the Old Woman Creek five kingdoms of living organisms (Margulis and estuary and watershed include the algal flora and the Schwartz 1988). As defined by Round (1969), this lower plants. For the purposes of the Site Profile, “algal grouping includes the major divisions (with typical flora” is considered as those chlorophyll-bearing, examples) listed in Table 6.1. aquatic organisms that lack vascular systems, true tissues, and root, stem, and leaf organs (Gray 1970) and “lower plants” include the fungi, lichens, mosses, horsetails, and ferns—those aquatic and terrestrial plant-like organisms with less complex vegetative and reproductive morphology than the gymnosperms (conifers) and angiosperms (flowering plants). In this profile, the grouping of species into divisions, classes, orders, and families follows the classification system presented in Synopsis and Classification of Living Organisms (Parker 1982), except where noted. TABLE 6.1. CLASSIFICATION OF ALGAL FLORA AND LOWER PLANTS Kingdom Monera Cyanobacteria (blue-green algae) Kingdom Protista Rhodophytes (red algae) Chrysophytes (golden & yellow-green algae) Pyrrhophytes (fire algae) Cryptophytes (crytomonads) Euglenophytes (euglenoids) Chlorophytes (green algae) Kingdom Fungi Myxomycetes (slime molds) Phycomycetes (algal fungi & water molds) Ascomysetes (yeasts, molds, & cup fungi) Figure 6.1. Phycology laboratory Basidiomycetes (mushrooms, smuts, & rusts) at the Ohio Center for Coastal Wetlands Study, Deuteromycetes (imperfect fungi) Old Woman Creek SNP & NERR (David M. -
Atp8 Is in the Ground Pattern of Flatworm Mitochondrial Genomes Bernhard Egger1* , Lutz Bachmann2 and Bastian Fromm3
Egger et al. BMC Genomics (2017) 18:414 DOI 10.1186/s12864-017-3807-2 RESEARCHARTICLE Open Access Atp8 is in the ground pattern of flatworm mitochondrial genomes Bernhard Egger1* , Lutz Bachmann2 and Bastian Fromm3 Abstract Background: To date, mitochondrial genomes of more than one hundred flatworms (Platyhelminthes) have been sequenced. They show a high degree of similarity and a strong taxonomic bias towards parasitic lineages. The mitochondrial gene atp8 has not been confidently annotated in any flatworm sequenced to date. However, sampling of free-living flatworm lineages is incomplete. We addressed this by sequencing the mitochondrial genomes of the two small-bodied (about 1 mm in length) free-living flatworms Stenostomum sthenum and Macrostomum lignano as the first representatives of the earliest branching flatworm taxa Catenulida and Macrostomorpha respectively. Results: We have used high-throughput DNA and RNA sequence data and PCR to establish the mitochondrial genome sequences and gene orders of S. sthenum and M. lignano. The mitochondrial genome of S. sthenum is 16,944 bp long and includes a 1,884 bp long inverted repeat region containing the complete sequences of nad3, rrnS, and nine tRNA genes. The model flatworm M. lignano has the smallest known mitochondrial genome among free- living flatworms, with a length of 14,193 bp. The mitochondrial genome of M. lignano lacks duplicated genes, however, tandem repeats were detected in a non-coding region. Mitochondrial gene order is poorly conserved in flatworms, only a single pair of adjacent ribosomal or protein-coding genes – nad4l-nad4 – was found in S. sthenum and M. lignano that also occurs in other published flatworm mitochondrial genomes. -
The Microscopic Anatomy of Lepidodermella Squamata (Dujardin, 1841)
Loyola University Chicago Loyola eCommons Master's Theses Theses and Dissertations 1977 The Microscopic Anatomy of Lepidodermella squamata (Dujardin, 1841) Raymond W. Ulbrich Loyola University Chicago Follow this and additional works at: https://ecommons.luc.edu/luc_theses Part of the Biology Commons Recommended Citation Ulbrich, Raymond W., "The Microscopic Anatomy of Lepidodermella squamata (Dujardin, 1841)" (1977). Master's Theses. 2967. https://ecommons.luc.edu/luc_theses/2967 This Thesis is brought to you for free and open access by the Theses and Dissertations at Loyola eCommons. It has been accepted for inclusion in Master's Theses by an authorized administrator of Loyola eCommons. For more information, please contact [email protected]. This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 License. Copyright © 1977 Raymond W. Ulbrich THE MICROSCOPIC ANATOMY OF LEPIDODERMELLA SQUAMATA (DUJARDIN, 1841) by Raymond W. Ulbrich A Thesis Submitted to the Faculty of the Graduate School of Loyola University of Chicago in Partial Fulfillment of the Requirements for the Degree of Master of Science December 1977 ACKNOWLEDGMENTS I would like to extend my thanks to the members of my thesis committee for their help and direction in the preparation of this work. The Director of my thesis was Dr. Clyde E. Robbins, and the other members of the committee were Fr. Walter P. Peters, S.J., and Dr. Boris E.N. Spiroff. My thanks are also extended to my family and friends for their support and encouragement. ii LIFE The author, Raymond W. Ulbrich, is the son of Edmund Peter Ulbrich and Willie Lucille (Gilmer) Ulbrich.