Palynology of the Permian Sanangoe
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S1. List of Taxa Included in the Disparity Analysis and the Phylogenetic Alysis, with Main References
S1. List of taxa included in the disparity analysis and the phylogenetic alysis, with main references. Taxa in bold are included in the phylogenetic analysis; taxa also indicated by * are included only in the phylogenetic analysis and not in the disparity analysis. Three unpublished arborescent taxa were included on the basis that they showed additional anatomical diversity. 1 Callixylon trunk from the Late Devonian of Marrocco showing large sclerotic nests in pith; 2 Axis from the late Tournaisian of Algeria, previously figured in Galtier (1988), and Galtier & Meyer-Berthaud (2006); 3 Trunk from the late Viséan of Australia. All these specimens and corresponding slides are currently kept in the Paleobotanical collections, Service des Collections, Université Montpellier II, France, under the specimen numbers 600/2/3, JC874 and YB1-2. Main reference Psilophyton* Banks et al., 1975 Aneurophytales Rellimia thomsonii Dannenhoffer & Bonamo, 2003; --- Dannenhoffer et al., 2007. Tetraxylopteris schmidtii Beck, 1957. Proteokalon petryi Scheckler & Banks, 1971. Triloboxylon arnoldii Stein & Beck, 1983. s m Archaeopteridales Callixylon brownii Hoskin & Cross, 1951. r e Callixylon erianum Arnold, 1930. p s o Callixylon huronensis Chitaley & Cai, 2001. n Callixylon newberry Arnold, 1931. m y g Callixylon trifilievii Lemoigne et al., 1983. o r Callixylon zalesskyi Arnold, 1930. P Callixylon sp. Meyer-Berthaud, unpublished data1. Eddya sullivanensis Beck, 1967. Protopityales Protopitys buchiana Scott, 1923; Galtier et al., 1998. P. scotica Walton, 1957. Protopitys sp. Decombeix et al., 2005. Elkinsiales Elkinsia polymorpha Serbet & Rothwell, 1992. Buteoxylales Buteoxylon gordonianum Barnard &Long, 1973; Matten et al., --- 1980. Triradioxylon primaevum Barnard & Long, 1975. Lyginopteridales Laceya hibernica May & Matten, 1983. Tristichia longii Galtier, 1977. -
SYSTÉMATIQUE DES EMBRYOPHYTES Document Illustrant Plus Particulièrement Les Taxons Européens Version 4 Octobre 2007
Université Pierre et Marie Curie (PARIS 6) Préparation à l’agrégation SVSTU, secteur B SYSTÉMATIQUE DES EMBRYOPHYTES Document illustrant plus particulièrement les taxons européens version 4 octobre 2007 Catherine Reeb, Préparation agrégation SVSTU, UPMC Jean-Yves Dubuisson, Laboratoire Paléobotanique et Paléoécologie, équipe Paléodiversité, systématique et évolution des Embryophytes, UPMC Dessin de couverture : extrait d’un traité botanique tibétain Pour Garance Remerciements: merci à Jean et Monique Duperon pour les clés de détermination des familles d’Angiospermes, à A.M pour la reproduction de couverture, à Michaël Manuel et Eric Queinnec pour la partie I de l’introduction. Egalement à tous les illustrateurs qui ont autorisé l’utilisation de leurs documents mis en ligne sur Internet : Françoise Gantet, Prof. I. Foissner, Association Endemia de Nouvelle Calédonie. 1 Table des matières Introduction 3 Les données essentielles pour l’agrégation . 5 I Systématique générale des Embryophytes 6 I.1 Caractères des Embryophytes . 6 I.2 La place des Embryophytes au sein de la lignée verte . 7 I.3 Le groupe frère des Embryophytes . 7 I.4 Relations au sein des Embryophytes :les points acquis aujourd’hui . 8 I.4.1 Marchantiophytes, Bryophytes, Anthocérotophytes à la base des Embryophytes . 8 I.4.2 Les Trachéophytes ou plantes vasculaires, un groupe monophylétique . 9 I.4.3 Les Spermatophytes ou plantes à ovules, un groupe monophylétique . 9 I.5 Quelques points encore en discussion . 11 I.5.1 Position et relations des trois clades basaux (Bryophytes, Marchantiophytes et Anthocérotophytes) 11 I.5.2 Relations au sein des Spermatophytes :l’hypothèse "Gnepine" . 13 II Les principaux clades d’Embryophytes 15 II.1 MARCHANTIOPHYTA:Les Marchantiophytes ou Hépatiques . -
System Klasyfikacji Organizmów
1 SYSTEM KLASYFIKACJI ORGANIZMÓW Nie ma dziś ogólnie przyjętego systemu klasyfikacji organizmów. Nie udaje się osiągnąć zgodności nie tylko w odniesieniu do zakresów i rang poszczególnych taksonów, ale nawet co do zasad metodologicznych, na których klasyfikacja powinna być oparta. Zespołowe dzieła przeglądowe z reguły prezentują odmienne i wzajemnie sprzeczne podejścia poszczególnych autorów, bez nadziei na consensus. Nie ma więc mowy o skompilowaniu jednolitego schematu klasyfikacji z literatury i system przedstawiony poniżej nie daje nadziei na zaakceptowanie przez kogokolwiek poza kompilatorem. Przygotowany został w oparciu o kilka zasad (skądinąd bardzo kontrowersyjnych): (1) Identyfikowanie ga- tunków i ich klasyfikowanie w jednostki rodzajowe, rodzinowe czy rzędy jest zadaniem specjalistów i bez szcze- gółowych samodzielnych studiów nie można kwestionować wyników takich badań. (2) Podział świata żywego na królestwa, typy, gromady i rzędy jest natomiast domeną ewolucjonistów i dydaktyków. Powody, które posłużyły do wydzielenia jednostek powinny być jasno przedstawialne i zrozumiałe również dla niespecjalistów, albowiem (3) podstawowym zadaniem systematyki jest ułatwianie laikom i początkującym badaczom poruszanie się w obezwładniającej złożoności świata żywego. Wątpliwe jednak, by wystarczyło to do stworzenia zadowalającej klasyfikacji. W takiej sytuacji można jedynie przypomnieć, że lepszy ułomny system, niż żaden. Królestwo PROKARYOTA Chatton, 1938 DNA wyłącznie w postaci kolistej (genoforów), transkrypcja nie rozdzielona przestrzennie od translacji – rybosomy w tym samym przedzia- le komórki, co DNA. Oddział CYANOPHYTA Smith, 1938 (Myxophyta Cohn, 1875, Cyanobacteria Stanier, 1973) Stosunkowo duże komórki, dwuwarstwowa błona (Gram-ujemne), wewnętrzna warstwa mureinowa. Klasa CYANOPHYCEAE Sachs, 1874 Rząd Stigonematales Geitler, 1925; zigen – dziś Chlorofil a na pojedynczych tylakoidach. Nitkowate, rozgałęziające się, cytoplazmatyczne połączenia mię- Rząd Chroococcales Wettstein, 1924; 2,1 Ga – dziś dzy komórkami, miewają heterocysty. -
Fundamentals of Palaeobotany Fundamentals of Palaeobotany
Fundamentals of Palaeobotany Fundamentals of Palaeobotany cuGU .叮 v FimditLU'φL-EjAA ρummmm 吋 eαymGfr 伊拉ddd仇側向iep M d、 況 O C O W Illustrations by the author uc削 ∞叩N Nn凹創 刊,叫MH h 咀 可 白 a aEE-- EEA First published in 1987 by Chapman αndHallLtd 11 New Fetter Lane, London EC4P 4EE Published in the USA by Chα~pman and H all 29 West 35th Street: New Yo地 NY 10001 。 1987 S. V. M秒len Softcover reprint of the hardcover 1st edition 1987 ISBN-13: 978-94-010-7916-7 e-ISBN-13: 978-94-009-3151-0 DO1: 10.1007/978-94-009-3151-0 All rights reserved. No part of this book may be reprinted, or reproduced or utilized in any form or by any electronic, mechanical or other means, now known or hereafter invented, including photocopying and recording, or in any information storage and retrieval system, without permission in writing from the publisher. British Library Cataloguing in Publication Data Mey凹, Sergei V. Fundamentals of palaeobotany. 1. Palaeobotany I. Title 11. Osnovy paleobotaniki. English 561 QE905 Library 01 Congress Catα loging in Publication Data Mey凹, Sergei Viktorovich. Fundamentals of palaeobotany. Bibliography: p. Includes index. 1. Paleobotany. I. Title. QE904.AIM45 561 8ι13000 Contents Foreword page xi Introduction xvii Acknowledgements xx Abbreviations xxi 1. Preservation 抄'pes αnd techniques of study of fossil plants 1 2. Principles of typology and of nomenclature of fossil plants 5 Parataxa and eutaxa S Taxa and characters 8 Peculiarity of the taxonomy and nomenclature of fossil plants 11 The binary (dual) system of fossil plants 12 The reasons for the inflation of generic na,mes 13 The species problem in palaeobotany lS The polytypic concept of the species 17 Assemblage-genera and assemblage-species 17 The cladistic methods 18 3. -
Article in Press
Türkiye Jeoloji Bülteni Geological Bulletin of Turkey 64 (2021) 267-276 doi: 10.25288/tjb.854704 The First Report of Gangamopteris rajaensis from Rajmahal Gondwana Basin (Jharkhand, India) Arun Joshi1 , Raj Kumar Priya2* 1 Council of Scientific and Industrial Research (CSIR) and SGRR (P.G.) College, Dehradun, India 2 Department of Geology, Sikkim University, Gangtok, Sikkim, India • Geliş/Received: 05.01.2021 • Düzeltilmiş Metin Geliş/Revised Manuscript Received: 13.05.2021 • Kabul/Accepted: 14.05.2021 • Çevrimiçi Yayın/Available online: 29.06.2021 • Baskı/Printed: 25.08.2021 Research Article/Araştırma Makalesi Türkiye Jeol. Bül. / Geol. Bull. Turkey Abstract: The present study deals with the systematic description of macro and miofloral analysis ofGangamopteris rajaensis and Glossopteris indica from the carbonaceous shale-coal bearing sequences of the Rajmahal Open Cast Mine, Rajmahal Basin, Jharkhand, India. The floral diversity, age correlation, and the paleoenvironment of the Barakar Formation were well described. Morphological analysis revealed the reticulate venation pattern, anastomosing of veins, and the absence of the midrib in Gangamopteris rajaensis. The recovered megafloral assemblages of Gangamopteris rajaensis and Glossopteris indica suggest a late early Permian (Artiskian-Kungurian) age for the Barakar strata of Rajmahal coal mine and the prevalence of a moderately warm climate during their deposition. Earlier the species was reported from the Barakar Formation of Damodar and Mahanadi Gondwana basins in India. However, this is the first detailed systematic investigation of this species from the Rajmahal Gondwana Basin, Jharkhand, India. Keywords: Barakar Formation, Early Permian, Gangamopteris rajaensis, Rajmahal Gondwana Basin. INTRODUCTION the Permo-Carboniferous period (Mukhopadhyay The warm and humid climate after the Late et al., 2010). -
Reproductive Biology of the Permian Glossopteridalesand Their
Proc. Natd. Acad. Sci. USA Vol. 89, pp. 11495-11497, December 1992 Plant Biology Reproductive biology of the Permian Glossopteridales and their suggested relationship to flowering plants (Gndwan/seed fen/p d peat/phogy) EDITH L. TAYLOR AND THOMAS N. TAYLOR Byrd Polar Research Center and Department of Plant Biology, Ohio State University, Columbus, OH 43210 Communicated by Henry N. Andrews, August 27, 1992 ABSTRACT The discovery of pn rid reproductive organs fm Le ard- mr Glacier regV_io Antarctica proides anato l eidene for the ada iat- tachment of the seeds to the megasporophyll in this Impant group of Late Paeooic seed plants. The position of the seeds is in direct contradiction to many earlier Pbs predominantly on impression/compressIon remains. The at- tachment of the ovules on the adaxial surface of a leaf-like megasftiorophyfl, combinedwithotherfetre, suchasm g- metophyte development, sugs a sler reproductive biology in this group than has prev been hypothesized. These findings confirm the of the Glessopteridales as seed ferns and are important coider- FIG. 1. Cross section of megasporophyll (below) showing three ato in dc ons f the of the group, cldg ovules attached to the adaxial (upper) surface. Arrow points to ovule phylogey that has been broken off and is reoriented with the micropyle facing their suggestd role as close relatives or possible c of the megasporophyll. Note circular pads of resistant tissue around the a osperms. micropyle. Arrowheads delimit outer edge of megasporophyll. (x15.) The Glossopteridales are a group of extinct gymnospermous plants that dominated many terrestrial habitats in Gondwana locality along Skaar Ridge in the Beardmore Glacier region of during Permian times. -
The Architecture of Permian Glossopterid Ovuliferous Reproductive Organs
Alcheringa: An Australasian Journal of Palaeontology ISSN: 0311-5518 (Print) 1752-0754 (Online) Journal homepage: https://www.tandfonline.com/loi/talc20 The architecture of Permian glossopterid ovuliferous reproductive organs Stephen Mcloughlin & Rose Prevec To cite this article: Stephen Mcloughlin & Rose Prevec (2019) The architecture of Permian glossopterid ovuliferous reproductive organs, Alcheringa: An Australasian Journal of Palaeontology, 43:4, 480-510, DOI: 10.1080/03115518.2019.1659852 To link to this article: https://doi.org/10.1080/03115518.2019.1659852 Published online: 01 Oct 2019. Submit your article to this journal Article views: 138 View related articles View Crossmark data Citing articles: 1 View citing articles Full Terms & Conditions of access and use can be found at https://www.tandfonline.com/action/journalInformation?journalCode=talc20 The architecture of Permian glossopterid ovuliferous reproductive organs STEPHEN MCLOUGHLIN and ROSE PREVEC MCLOUGHLIN,S.&PREVEC, R. 20 September 2019. The architecture of Permian glossopterid ovuliferous reproductive organs. Alcheringa 43, 480–510. ISSN 0311-5518 A historical account of research on glossopterid ovuliferous reproductive structures reveals starkly contrasting interpretations of their architecture and homologies from the earliest investigations. The diversity of interpretations has led to the establishment of a multitude of genera for these fossil organs, many of the taxa being synonymous. We identify a need for taxonomic revision of these genera to clearly demarcate taxa before they can be used effectively as palaeobiogeographic or biostratigraphic indices. Our assessment of fructification features based on extensive studies of adpression and permineralized fossils reveals that many of the character states for glossopterids used in previous phylogenetic analyses are erroneous. -
Early Permian Palaeofloras from Southern Brazilian Gondwana: a Palaeoclimatic Approach
Revista Brasileira de Geociências 30(3):486-490, setembro de 2000 EARLY PERMIAN PALAEOFLORAS FROM SOUTHERN BRAZILIAN GONDWANA: A PALAEOCLIMATIC APPROACH MARGOT GUERRA-SOMMER AND MIRIAM CAZZULO-KLEPZIG ABSTRACT In evaluating the parameters supplied by the taphofloras from different sedimentary facies in the Early Permian sedimentary sequences of the southern part of the Paraná basin, Brazil, it has become evident that the palaeofloristic evolution was related to palaeoecological and palaeoclimatic evolution. The homogeneous composition of Early Permian floral assemblages, which are characterized mainly by herbaceous to shrub-like plants considered to be relicts from the rigorous climate of an ice age (e.g. Botrychiopsis plantiana) suggest the persistence of the cold climate. The dominance of Rubidgea and Gangamopteris leaves with palmate venation associated with glossopterids with penate venation seems to indicate a gradual warming of climate. In roof-shales of coalbearing strata pinnate glossopterids related to Glossopteris are common, while Gangamopteris and Rubidgea (palmate forms) are poorly represented. The sudden enrichment of herbaceous articulates and filicoids fronds is characteristic of this stage and trunks of arborescents lycophytes become important elements. These antrocophilic paleofloras are characterized by typical elements of the "Glossopteris flora" associated to tree lycophytes and ferns communities. Therefore, the cool seasonal climate of Early Permian changed into the moist seasonal interval during the Artinskian-Kungurian. This climatic change was significant to the meso-hygrophitic to hygrophitic vegetation registered in roof-shale ferns of the Gondwana Southern Brazilian coalbearing strata. Keywords: roof-shale floras, Gondwana, Southern Brazil, Paraná basin, Glossopteris Flora INTRODUCTION The intracratonic Paraná basin, with a total area proposed by Milani et al. -
Morphology and Affinities of Glossopteris
MORPHOLOGY AND AFFINITIES OF GLOSSOPTERIS K. R. SURANGE & SHALLA CHANDRA Birbal Sahni Institute of Palaeobotany, Lucknow-226007, India ABSTRACT Reproductive organs of glossopterids, viz., Eretmonia, Glossotlleea, Kendos• trobus, Lidgettonia, Partlla, Russangea, M ooia, Rigbya, Denkania, Venustostrobus, Plumsteadiostrobus, Dietyopteridium and Jambadostrobus are briefly described. Their morphology and affinities are discussed. In the Permian of the southern hemis• phere atleast two distinct orders of gymnosperms, viz., Pteridospermales and Glos• sopteridales were dominating the landscape. genera bore sporangia terminally on ultimate GLOSSOPTERISAustralia were firstleavesrecordedfrom Indiaby Brong•and branches whereas the third genus bore niart in 1828. From 1845 to 1905, sporangia crowded on a cylindrical axis. a number of new species of Glossopteris were discovered from different continents of Eretmonia Du Toit Gondwanaland. From 1905 to 1950 there PI. 1. figs. 3,4; PI. 2, fig. 2; PI. 3, figs. 2,3 were only a few records, but from 1950 onwards Glossopteris again attracted the Fertile scale leaves of Eretmonia (see attention of many palaeobotanists. At first, Chandra & Surange, 1977, text-fig. 1) are of Glos90pteris were regarded as ferns but different shapes and sizes and five species later they turned out to be seed .plants. have been recognized on this basis. The In recent years our knowledge of the fertile bracts are ovate (E. ovoides Surange reproductive structures of glossopterids has & Chandra, 1974), spathulate with acute increased to such an extent that one can apex (E. hingridaensis Surange & Mahesh• get some idea as to what type of plants wari, 1970), triangular (E. emarginata they were. Chandra & Surange, 1977), diamond-shaped (E. utkalensis Surange & Maheshwari, 1970) HABIT and orbicular (E. -
New Glossopterid Polysperms from the Permian La Golondrina Formation (Santa Cruz Province, Argentina): Potential Affinities and Biostratigraphic Implications
Rev. bras. paleontol. 18(3):379-390, Setembro/Dezembro 2015 © 2015 by the Sociedade Brasileira de Paleontologia doi: 10.4072/rbp.2015.3.04 NEW GLOSSOPTERID POLYSPERMS FROM THE PERMIAN LA GOLONDRINA FORMATION (SANTA CRUZ PROVINCE, ARGENTINA): POTENTIAL AFFINITIES AND BIOSTRATIGRAPHIC IMPLICATIONS BÁRBARA CARIGLINO Museo Argentino de Ciencias Naturales “Bernardino Rivadavia”, CONICET, Av. Ángel Gallardo 470, C1405DJR, Buenos Aires, Argentina. [email protected] ABSTRACT – Impression fossils of ovuliferous fructifi cations from the Permian La Golondrina Formation in Santa Cruz, Argentina, are described, their affi nities compared, and fi nally, assigned to the Arberiaceae (Glossopteridales). Based on morphological differences from the genera in Arberiaceae, a new taxon is established for some specimens, whereas others are allocated to Arberia madagascariensis (Appert) Anderson & Anderson. This is the fi rst record of Arberiaceae from the La Golondrina Basin. The biostratigraphic implications of the occurrence of this family in this unit are discussed, and suggest that more evidence other than that provided by the megafl oral elements is needed to resolve the age of the constituent members of the La Golondrina Formation. Key words: Arberiaceae, Argentina, biostratigraphy, fructifi cations, Glossopteridales, Gondwana. RESUMO – São descritos impressões fósseis de frutifi cações femininas provenientes da Formação La Golondrina, Permiano de Santa Cruz (Argentina), atribuídas a Arberiaceae (Glossopteridales), segundo a comparação de suas afi nidades. -
1 Relationships of Angiosperms To
Relationships of Angiosperms to 1 Other Seed Plants Seed plants are of fundamental importance both evolution- all gymnosperms (living and extinct) together are not arily and ecologically. They dominate terrestrial landscapes, monophyletic. Importantly, several fossil lineages, Cayto- and the seed has played a central role in agriculture and hu- niales, Bennettitales, Pentoxylales, and Glossopteridales man history. There are fi ve extant lineages of seed plants: (glossopterids), have been proposed as putative close rela- angiosperms, cycads, conifers, gnetophytes, and Ginkgo. tives of the angiosperms based on phylogenetic analyses These fi ve groups have usually been treated as distinct (e.g., Crane 1985; Rothwell and Serbet 1994; reviewed in phyla — Magnoliophyta (or Anthophyta), Cycadophyta, Doyle 2006, 2008, 2012; Friis et al. 2011). These fossil lin- Co ni fe ro phyta, Gnetophyta, and Ginkgophyta, respec- eages, sometimes referred to as the para-angiophytes, will tively. Cantino et al. (2007) used the following “rank- free” therefore be covered in more detail later in this chapter. An- names (see Chapter 12): Angiospermae, Cycadophyta, other fossil lineage, the corystosperms, has been proposed Coniferae, Gnetophyta, and Ginkgo. Of these, the angio- as a possible angiosperm ancestor as part of the “mostly sperms are by far the most diverse, with ~14,000 genera male hypothesis” (Frohlich and Parker 2000), but as re- and perhaps as many as 350,000 (The Plant List 2010) to viewed here, corystosperms usually do not appear as close 400,000 (Govaerts 2001) species. The conifers, with ap- angiosperm relatives in phylogenetic trees. proximately 70 genera and nearly 600 species, are the sec- The seed plants represent an ancient radiation, with ond largest group of living seed plants. -
Cuencas Sedimentarias De Uruguay: Geología, Paleontología Y Recursos Naturales
UNIVERSIDAD DE LA REPÚBLICA – FACULTAD DE CIENCIAS CUENCAS SEDIMENTARIAS DE URUGUAY Geología, paleontología y recursos naturales PALEOZOICO GERARDO VEROSLAVSKY – MARTÍN UBILLA SERGIO MARTÍNEZ EDITORES GLORIA DANERS JORGE MONTAÑO HÉCTOR DE SANTA ANA ETHEL MORALES VICENTE FULFARO ROSSANA MUZIO CÉSAR GOSO AGUILAR ELENA PEEL NORA LORENZO ANDRÉS PÉREZ HENRI MASQUELIN GRACIELA PIÑEIRO EDUARDO ROSSELLO DI.R.A.C. Montevideo – Uruguay 2006 Cuencas sedimentarias de Uruguay: Geología, paleontología y recursos naturales. Paleozoico / Gerardo Veroslavsky, Martín Ubilla, Sergio Martínez, editores.– Montevideo: DI.R.A.C., 2006. 326 pp. : il., cuadros, mapas y fotos. ISBN: 9974-0-0316-4 1. URUGUAY 2. GEOLOGÍA 3. PALEONTOLOGÍA 4. PALEOZOICO 5. GEOLOGÍA HISTÓRICA I. Veroslavsky, Gerardo, ed. II. Ubilla, Martín, ed. III. Martínez, Sergio, ed. 551.77(899) CDU Edición del texto y notas complementarias: Luis Elbert. Diseño de tapas, tratamiento de gráficos y puesta en página: Gabriel Santoro. Figura de tapa: adaptación del Geological Map of the World, 1849, de James Reynolds (ed.) incluido en el libro The image of the world de Peter Whitfield. Pomegranate Artbooks, San Francisco 1994. Figura de contratapa: fragmento del Mapa tectónico de América del Sur, Commission for the Geological Map of the World (CGMW) 1978, UNESCO. Edición DI.R.A.C. (División Relaciones y Actividades Culturales de Facultad de Ciencias) Calle Iguá 4225 – Montevideo 11400 – Uruguay Tel. (+598) 25251711 – Fax (+598) 25258617 e-mail: [email protected] 2006 DIRAC – Facultad de Ciencias Esta obra está bajo una Licencia Creative Commons Atribución-NoComercial-SinDerivadas 4.0 Internacional ÍNDICE Prefacio 5 Autores 8 Capítulo I: El Paleozoico. 11 Gerardo Veroslavsky, Sergio Martínez y Martín Ubilla Capítulo II: El Escudo Uruguayo.