Msc Part -1 PAPER – 4 TOPIC- Bryophytes
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Genetic Analysis of the Liverwort Marchantia Polymorpha Reveals That
Research Genetic analysis of the liverwort Marchantia polymorpha reveals that R2R3MYB activation of flavonoid production in response to abiotic stress is an ancient character in land plants Nick W. Albert1 , Amali H. Thrimawithana2 , Tony K. McGhie1 , William A. Clayton1,3, Simon C. Deroles1 , Kathy E. Schwinn1 , John L. Bowman4 , Brian R. Jordan3 and Kevin M. Davies1 1The New Zealand Institute for Plant & Food Research Limited, Private Bag 11600, Palmerston North, New Zealand; 2The New Zealand Institute for Plant & Food Research Limited, Private Bag 92169, Auckland Mail Centre, Auckland 1142, New Zealand; 3Faculty of Agriculture and Life Sciences, Lincoln University, Christchurch 7647, New Zealand; 4School of Biological Sciences, Monash University, Melbourne, Victoria 3800, Australia Summary Author for correspondence: The flavonoid pathway is hypothesized to have evolved during land colonization by plants Kevin M. Davies c. 450 Myr ago for protection against abiotic stresses. In angiosperms, R2R3MYB transcription Tel: +64 6 3556123 factors are key for environmental regulation of flavonoid production. However, angiosperm Email: [email protected] R2R3MYB gene families are larger than those of basal plants, and it is not known whether the Received: 29 October 2017 regulatory system is conserved across land plants. We examined whether R2R3MYBs regulate Accepted: 19 December 2017 the flavonoid pathway in liverworts, one of the earliest diverging land plant lineages. We characterized MpMyb14 from the liverwort Marchantia polymorpha using genetic New Phytologist (2018) 218: 554–566 mutagenesis, transgenic overexpression, gene promoter analysis, and transcriptomic and doi: 10.1111/nph.15002 chemical analysis. MpMyb14 is phylogenetically basal to characterized angiosperm R2R3MYB flavonoid regulators. Key words: CRISPR/Cas9, evolution, Mpmyb14 knockout lines lost all red pigmentation from the flavonoid riccionidin A, flavonoid, liverwort, MYB, stress. -
Novelties in the Hornwort Flora of Croatia and Southeast Europe
cryptogamie Bryologie 2019 ● 40 ● 22 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 -
Phytotaxa, a Synthesis of Hornwort Diversity
Phytotaxa 9: 150–166 (2010) ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ Article PHYTOTAXA Copyright © 2010 • Magnolia Press ISSN 1179-3163 (online edition) A synthesis of hornwort diversity: Patterns, causes and future work JUAN CARLOS VILLARREAL1 , D. CHRISTINE CARGILL2 , ANDERS HAGBORG3 , LARS SÖDERSTRÖM4 & KAREN SUE RENZAGLIA5 1Department of Ecology and Evolutionary Biology, University of Connecticut, 75 North Eagleville Road, Storrs, CT 06269; [email protected] 2Centre for Plant Biodiversity Research, Australian National Herbarium, Australian National Botanic Gardens, GPO Box 1777, Canberra. ACT 2601, Australia; [email protected] 3Department of Botany, The Field Museum, 1400 South Lake Shore Drive, Chicago, IL 60605-2496; [email protected] 4Department of Biology, Norwegian University of Science and Technology, N-7491 Trondheim, Norway; [email protected] 5Department of Plant Biology, Southern Illinois University, Carbondale, IL 62901; [email protected] Abstract Hornworts are the least species-rich bryophyte group, with around 200–250 species worldwide. Despite their low species numbers, hornworts represent a key group for understanding the evolution of plant form because the best–sampled current phylogenies place them as sister to the tracheophytes. Despite their low taxonomic diversity, the group has not been monographed worldwide. There are few well-documented hornwort floras for temperate or tropical areas. Moreover, no species level phylogenies or population studies are available for hornworts. Here we aim at filling some important gaps in hornwort biology and biodiversity. We provide estimates of hornwort species richness worldwide, identifying centers of diversity. We also present two examples of the impact of recent work in elucidating the composition and circumscription of the genera Megaceros and Nothoceros. -
Anthocerotophyta
Glime, J. M. 2017. Anthocerotophyta. Chapt. 2-8. In: Glime, J. M. Bryophyte Ecology. Volume 1. Physiological Ecology. Ebook 2-8-1 sponsored by Michigan Technological University and the International Association of Bryologists. Last updated 5 June 2020 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology/>. CHAPTER 2-8 ANTHOCEROTOPHYTA TABLE OF CONTENTS Anthocerotophyta ......................................................................................................................................... 2-8-2 Summary .................................................................................................................................................... 2-8-10 Acknowledgments ...................................................................................................................................... 2-8-10 Literature Cited .......................................................................................................................................... 2-8-10 2-8-2 Chapter 2-8: Anthocerotophyta CHAPTER 2-8 ANTHOCEROTOPHYTA Figure 1. Notothylas orbicularis thallus with involucres. Photo by Michael Lüth, with permission. Anthocerotophyta These plants, once placed among the bryophytes in the families. The second class is Leiosporocerotopsida, a Anthocerotae, now generally placed in the phylum class with one order, one family, and one genus. The genus Anthocerotophyta (hornworts, Figure 1), seem more Leiosporoceros differs from members of the class distantly related, and genetic evidence may even present -
The Gemma of (Marchantiaceae, Marchantiophyta)
蘚苔類研究(Bryol. Res.) 12(1): 1‒5, July 2019 The gemma of Marchantia pinnata (Marchantiaceae, Marchantiophyta) Tian-Xiong Zheng and Masaki Shimamura Laboratory of Plant Taxonomy and Ecology, Graduate School of Integrated Sciences for Life, Hiroshima University, 1‒3‒1 Kagamiyama, Higashihiroshima-shi, Hiroshima 739‒8526, Japan Abstract. The novel morphology of gemma in Marchantia pinnata Steph., an endemic species to east Asia, is reported for the first time. The outer shape of gemma is gourd-like with maximum width ca. 250 µm and length ca. 350 µm. The surface is not smooth due to the swelling of the cells. The margin of gemmae is never entire due to mammillose and with several papillae on marginal cells. The two apical notches have no mucilage hairs. These morphologies are widely different from those of a com- mon species, M. polymorpha subsp. ruderalis with larger and nearly circular in outer shape, entire margin and mucilage hairs in notches. Morphological characters of gemmae might be useful for the identification of Marchantia species. Key words: Marchantiaceae, Marchantia pinnata, gemma, mucilage hair 鄭天雄・嶋村正樹:ヒトデゼニゴケの無性芽(〒739‒8526 広島県東広島市鏡山1‒3‒1 広島大学大学院 統合生命科学研究科 植物分類・生態学研究室) 東アジア固有種であるヒトデゼニゴケ Marchantia pinnata Steph. の無性芽の形態について報告する. ヒトデゼニゴケの無性芽は,ひょうたん型の外形を持ち,長さと幅の最大値はそれぞれ350 µm,250 µm 程度,二つのノッチには粘液毛がない.また,無性芽の縁の細胞は円錐状のマミラを持ち,パピラが散 在する.これらの形態は,ほぼ円形でより大きな外形を持ち,縁が全縁,ノッチに粘液毛を有するゼニ ゴケの無性芽とは明らかに異なる.ゼニゴケ属における無性芽の形態の多様性は,種を識別するための 有用な形質として扱えるかもしれない. gemmae is multicellular discoid structure with two Introduction laterally placed apical notches. The central part is several cells thick and becomes gradually thinner to- The asexual reproduction propagule, organ gem- ward the unistratose margin(Shimamura 2016). mae shows the high morphological diversity for each Marchantia pinnana Steph., an endemic species of taxon of liverworts. -
Morphology, Anatomy and Reproduction of Anthoceros
Morphology, Anatomy and Reproduction of Anthoceros - INDRESH KUMAR PANDEY Taxonomic Position of Anthoceros Class- Anthocerotopsida Single order Anthocerotales Two families Anthocerotaceae Notothylaceae Representative Genus Anthoceros Notothylus General features of Anthocerotopsida • Forms an isolated evolutionary line • Sometimes considered independent from Bryophytes and placed in division Anthocerophyta • Called as Hornworts due to horn like structure of sporophyte • Commonly recognised genera includes Anthoceros, Megaceros, Nothothylus, Dendroceros Anthoceros :Habitat & Distribution • Cosmopolitan • Mainly in temperate & tropical regions • More than 200 species, 25 sp. Recorded from India. • Mostly grows in moist shady places, sides of ditches or in moist hollows among rocks • Few species grow on decaying wood. • Three common Indian species- A. erectus, A. crispulus, A. himalayensis Anthoceros: Morphology Dorsal surface Ventral surface Rhizoids (smooth walled) Thallus showing tubers External features • Thallus (gametophyte)- small, dark green, dorsiventral, prostrate, branched or lobed • No midrib, spongy due to presence of underlying mucilaginous ducts • Dorsal surface varies from species to species Smooth- A. laevis Velvety- A. crispulus Rough- A. fusiformis • Smooth walled rhizoid on ventral surface • Rounded bluish green thickened area on ventral surface- Nostoc colonies Internal structure Vertical Transverse Section- Diagrammatic Vertical Transverse Section- Cellular Internal Structure • Simple, without cellular differentiation -
Establishment of Anthoceros Agrestis As a Model Species for Studying the Biology of Hornworts
Szövényi et al. BMC Plant Biology (2015) 15:98 DOI 10.1186/s12870-015-0481-x METHODOLOGY ARTICLE Open Access Establishment of Anthoceros agrestis as a model species for studying the biology of hornworts Péter Szövényi1,2,3,4†, Eftychios Frangedakis5,8†, Mariana Ricca1,3, Dietmar Quandt6, Susann Wicke6,7 and Jane A Langdale5* Abstract Background: Plants colonized terrestrial environments approximately 480 million years ago and have contributed significantly to the diversification of life on Earth. Phylogenetic analyses position a subset of charophyte algae as the sister group to land plants, and distinguish two land plant groups that diverged around 450 million years ago – the bryophytes and the vascular plants. Relationships between liverworts, mosses hornworts and vascular plants have proven difficult to resolve, and as such it is not clear which bryophyte lineage is the sister group to all other land plants and which is the sister to vascular plants. The lack of comparative molecular studies in representatives of all three lineages exacerbates this uncertainty. Such comparisons can be made between mosses and liverworts because representative model organisms are well established in these two bryophyte lineages. To date, however, a model hornwort species has not been available. Results: Here we report the establishment of Anthoceros agrestis as a model hornwort species for laboratory experiments. Axenic culture conditions for maintenance and vegetative propagation have been determined, and treatments for the induction of sexual reproduction and sporophyte development have been established. In addition, protocols have been developed for the extraction of DNA and RNA that is of a quality suitable for molecular analyses. -
About the Book the Format Acknowledgments
About the Book For more than ten years I have been working on a book on bryophyte ecology and was joined by Heinjo During, who has been very helpful in critiquing multiple versions of the chapters. But as the book progressed, the field of bryophyte ecology progressed faster. No chapter ever seemed to stay finished, hence the decision to publish online. Furthermore, rather than being a textbook, it is evolving into an encyclopedia that would be at least three volumes. Having reached the age when I could retire whenever I wanted to, I no longer needed be so concerned with the publish or perish paradigm. In keeping with the sharing nature of bryologists, and the need to educate the non-bryologists about the nature and role of bryophytes in the ecosystem, it seemed my personal goals could best be accomplished by publishing online. This has several advantages for me. I can choose the format I want, I can include lots of color images, and I can post chapters or parts of chapters as I complete them and update later if I find it important. Throughout the book I have posed questions. I have even attempt to offer hypotheses for many of these. It is my hope that these questions and hypotheses will inspire students of all ages to attempt to answer these. Some are simple and could even be done by elementary school children. Others are suitable for undergraduate projects. And some will take lifelong work or a large team of researchers around the world. Have fun with them! The Format The decision to publish Bryophyte Ecology as an ebook occurred after I had a publisher, and I am sure I have not thought of all the complexities of publishing as I complete things, rather than in the order of the planned organization. -
02-Bryophyta-2.Pdf
498 INTRODUCTORY PLANT SCIENCE layer. In certain species, the capsule con til1Ues to grow as long as the gametophyte lives. The presence of a meristcm in A11tlioceros and an aerating system complete with sto mata may indicate that Antlwceros evolved from ancestors with even ·larger· and more 1. Civ complex sporophytes. These features may Bryophyt be vestiges from a more complex ancestral. 2. Wh sporophyte. that ti alga ? 3. De� ORIGIN AND RELATIONSHIPS OF THE Bryophyt, BRYOPHYTA 4._ characteri Little is known with certainty about the r are small origin and evolution of the bryophytes. The ' tall. ( B) fossil record is too fragmenta to enable • ry s true roots us to trace their evolutionary history. Frag ,, sperms ar mentary remnants of thallose liverworts, spore idium and mother\4'/ttN) which resemble present-day liverworts, have cell Jar arch� been foum! in rocks of Carboniferous age, bryophyt as have structures that may be remains of more com mosses. all bryoph The immediate ancestors of the bryo bryo whicl phytes were probably more complex plants from the have an i than present-day forms. In other words, the gametophy evolutionary tendency has been one of re- with a dip1 duction instead of increased complexity. •• • • • spores If evolution has progressed . from more • . •, .... • s. __ complex sporophytes to those of simpler • . vascular p Anthoceros . form, the sporophyte of wou1d • • green algat be considered more ancient than that of • (D) red Marchantia or Riccia. Because Riccia has Fig. 35-16. longitudinal section of the spo 6. How the most reduced sporophyte, it would be t·:i;,hyte of Anthoceros. -
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............................................................................................... -
Of Mount Sibayak North Sumatra, Indonesia Marchantia
BIOTROPIA Vol. 20 No. 2, 2013: 73 - 80 DOI: 10.11598/btb.2013.20.2.3 THE LIVERWORT GENUS MARCHANTIA (MARCHANTIACEAE) OF MOUNT SIBAYAK NORTH SUMATRA, INDONESIA ETTI SARTINA SIREGAR1,2 , NUNIK S. ARIYANTI 3 , and SRI S.TJITROSOEDIRDJO3,4 1 Plant Biology Graduate Program, Graduate School, Bogor Agricultural University, IPB-Campus Darmaga, Bogor, Indonesia 2University of Sumatra Utara, Medan, Indonesia 3Department of Biology, Faculty of Mathematics and Natural Sciences, Bogor Agricultural University, IPB-Campus Darmaga, Bogor Indonesia 4 SEAMEO BIOTROP, Jl. Raya Tajur km 6, Bogor, Indonesia Received 21 January 2013/Accepted 02 July 2013 ABSTRACT Knowledge on the liverworts (Marchantiophyta) flora of Sumatra is very scanty including that of genusMarchantia (Marchantiaceae). This study was conducted to explore the diversity of Marchantia in Mount Sibayak North Sumatra, Indonesia. Altogether, seven species of Marchantia are found in Mount Sibayak North Sumatra, of which five are previously known (Marchantia acaulis , M. emarginata , M. geminata , M. paleacea , and M. treubii ), while one is as new species record (M. polymorpha ) for Sumatra, and one species has not been identified ( Marchantia sp. ). An identification key to the species of Marchantia from Sumatra is provided. Key words: Liverwort,Marchantia , Marchantiaceae, Mount Sibayak, North Sumatra INTRODUCTION Marchantia L. is one of the largest genera in the liverworts order Marchantiales. This genus is represented by 36 species found in the world (Bischler-Causse 1998). In Indonesia especially Sumatra, the floristic work onMarchantia is still very scarce. Herzog (1943) in his study of liverworts from Sumatra, recorded three species of Marchantia,namely M. emarginata , M. mucilaginosa and M. -
Anthocerotophyta) of Colombia
BOTANY https://dx.doi.org/10.15446/caldasia.v40n2.71750 http://www.revistas.unal.edu.co/index.php/cal Caldasia 40(2):262-270. Julio-diciembre 2018 Key to hornworts (Anthocerotophyta) of Colombia Clave para Antocerotes (Anthocerotophyta) de Colombia S. ROBBERT GRADSTEIN Muséum National d’Histoire Naturelle, Institut de Systématique, Evolution, Biodiversité (UMR 7205), Paris, France. [email protected] ABSTRACT A key is presented to seven genera and fifteen species of hornworts recorded from Colombia. Three species found in Ecuador but not yet in Colombia (Dendroceros crispatus, Phaeomegaceros squamuligerus, and Phaeoceros tenuis) are also included in the key. Key words. Biodiversity, identification, taxonomy. RESUMEN Se presenta una clave taxonómica para los siete géneros y quince especies de antocerotes registrados en Colombia. Tres especies registradas en Ecuador, pero aún no en Colombia (Dendroceros crispatus, Phaeomegaceros squamuligerus y Phaeoceros tenuis), también son incluidas. Palabras clave. Biodiversidad, identificación, taxonomía. INTRODUCCIÓN visible as black dots, rarely as blue lines (in Leiosporoceros); chloroplasts large, Hornworts (Anthocerotophyta) are a small 1–2(–4) per cell, frequently with a pyrenoid; division of bryophytes containing about 192 2) gametangia immersed in the thallus, accepted species worldwide (excluding 28 originating from an inner thallus cell; 3) doubtful species), in five families and 12 sporophyte narrowly cylindrical, without genera (Villarreal and Cargill 2016). They seta; 4) sporophyte growth by means of are commonly found on soil in rather open a basal meristem; 5) spore maturation places, but also on rotten logs, rock, bark asynchronous; and 6) capsule dehiscence or on living leaves. Hornworts were in the gradual, from the apex slowly downwards, past often classified with the liverworts by means of 2(-4) valves, rarely by an because of their superficial resemblance to operculum.