Brown Algae Phaeophyta II
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A Revision of Schoenobryum (Cryphaeaceae, Bryopsida) in Africa1
Revision of Schoenobryum 147 Tropical Bryology 24: 147-159, 2003 A revision of Schoenobryum (Cryphaeaceae, Bryopsida) in Africa1 Brian J. O’Shea 141 Fawnbrake Avenue, London SE24 0BG, U.K. Abstract. The nine species and two varieties of Schoenobryum reported for Africa were investigated, and no characters were found that uniquely identified any of the taxa to be other than the pantropical Schoenobryum concavifolium. The following nine names become new synonyms of S. concavifolium: Cryphaea madagassa, C. subintegra, Acrocryphaea robusta, A. latifolia, A. subrobusta, A. tisserantii, A. latifolia var. microspora, A. plicatula and A. subintegra var. idanreense; a lectotype is selected for Acrocryphaea latifolia var. microspora P.de la Varde. INTRODUCTION as the majority have not been examined since the type description, and many have never been A recent checklist of Sub-Saharan Africa illustrated. (O’Shea, 1999) included nine species and two varieties of Schoenobryum, most of quite limited The purpose of this paper is to provide an distribution. Recent collecting in both Malawi overview of the genus worldwide, and to review (O’Shea et al., 2001) and Uganda (Wigginton et the taxonomic position of the African taxa. al., 2001) has shown the genus to be not uncommon, although there was only one CRYPHAEACEAE SCHIMP. 1856. previously published collection from the two countries (O’Shea, 1993). Apart from one Cryphaeaceae Schimp., Coroll. Bryol. Eur. 97. African taxon occurring in nine countries, the 1856 [‘1855’]. Type: Cryphaea D.Mohr in other 10 occurred in an average of 1.7 countries. F.Weber This particular profile is typical of unrevised genera in Africa, and indicative of a possible A brief review of the circumscription and need for revision (O’Shea, 1997), particularly systematics of the family, and the distinctions from related families (e.g. -
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 -
Volume 1, Chapter 2-7: Bryophyta
Glime, J. M. 2017. Bryophyta – Bryopsida. Chapt. 2-7. In: Glime, J. M. Bryophyte Ecology. Volume 1. Physiological Ecology. Ebook 2-7-1 sponsored by Michigan Technological University and the International Association of Bryologists. Last updated 10 January 2019 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology/>. CHAPTER 2-7 BRYOPHYTA – BRYOPSIDA TABLE OF CONTENTS Bryopsida Definition........................................................................................................................................... 2-7-2 Chromosome Numbers........................................................................................................................................ 2-7-3 Spore Production and Protonemata ..................................................................................................................... 2-7-3 Gametophyte Buds.............................................................................................................................................. 2-7-4 Gametophores ..................................................................................................................................................... 2-7-4 Location of Sex Organs....................................................................................................................................... 2-7-6 Sperm Dispersal .................................................................................................................................................. 2-7-7 Release of Sperm from the Antheridium..................................................................................................... -
Bangor University DOCTOR of PHILOSOPHY Biosystematic and Cytological Studies of Mosses and Liverworts. Abderrahman, Salim Moh'd
Bangor University DOCTOR OF PHILOSOPHY Biosystematic and cytological studies of mosses and liverworts. Abderrahman, Salim Moh'd Mansur Award date: 1981 Link to publication General rights Copyright and moral rights for the publications made accessible in the public portal are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. • Users may download and print one copy of any publication from the public portal for the purpose of private study or research. • You may not further distribute the material or use it for any profit-making activity or commercial gain • You may freely distribute the URL identifying the publication in the public portal ? Take down policy If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. Download date: 05. Oct. 2021 In the name of GOD Most Gracious Most Merciful -ii iä -0 Thanking Him with a full heart and devoted tongue ST COPY AVAILA L TEXT IN ORIGINAL IS CLOSETO THE EDGE OF THE PAGE BIOSYSTE14ATIC'AND'CYTOLOGICAL', STUDIES'OF 'MOSSES'AND 'LIVERWORTS A thesis Presented for the &gree pf- PhiloSophiae Doctor in the University of Wales by Salim Moh'd Mansur Abderrahmano B. Sc. Biology & Ed. Cý (Kuwait University) School of Plant Biology, University College of North Wales, Bangor M. K. ), I hereby declare that the work herein, now submitted as a thesis for the degree of Philosophiae Doctor of the University of Wales, is the result of my own investigations and that all references to ideas and work of other resefrchers has been specifically acknoFledged. -
Axenically Culturing the Bryophytes: Establishment and Propagation of the Moss Hypnum Cupressiforme Hedw. (Bryophyta, Hypnaceae) in in Vitro Conditions
35 (1): (2011) 71-77 Original Scientifi c Paper Axenically culturing the bryophytes: establishment and propagation of the moss Hypnum cupressiforme Hedw. (Bryophyta, Hypnaceae) in in vitro conditions Milorad Vujičić✳, Aneta Sabovljević and Marko Sabovljević Institute of Botany and Garden, Faculty of Biology, University of Belgrade, Takovska 43, 11000 Belgrade, Serbia ABSTRACT: Th e study gives the fi rst report of in vitro culture of the pleurocarpous moss Hypnum cupressiforme and on the problems of axenicaly culturing this bryophyte and the conditions for establishment and propagation. Problems of surface sterilization are elaborated regarding sporophyte vs. gametophyte. Th e infl uence of nutrient, light length and temperature on diff erent developmental stages is discussed. Th e best conditions for micro-propagation from shoots are slightly lower temperature (18-20°C), on MS-sugar free medium irrelevant of day length. Th is moss is a counterpart of some rare and endangered mosses from the same genus and data presented should be taken into account of conservation and propagation of its counterparts as well. Its propagation is valuable for horticultural, pharmaceutical and bioindication purposes, as well. Key words: moss, Hypnum cupressiforme, in vitro, development, propagation Received 29 October 2010 Revision accepted 27 December 2010 UDK 582.325.23:575.2.085.2 INTRODUCTION establishment in axenic culture, it is oft en problem of material availability, genetic variability of material, disposal Bryophytes (comprising hornworts, liverworts and of axenic organisms leaving on bryophytes and low level mosses) are the second largest group of higher plants aft er of species biology knowledge (e.g. Duckett et al. -
(Bryopsida: Splachnaceae). Lily Roberta Lewis University of Connecticut, [email protected]
University of Connecticut OpenCommons@UConn Doctoral Dissertations University of Connecticut Graduate School 5-7-2015 Resolving Amphitropical Phylogeographic Histories in the Common Dung Moss Tetraplodon (Bryopsida: Splachnaceae). Lily Roberta Lewis University of Connecticut, [email protected] Follow this and additional works at: https://opencommons.uconn.edu/dissertations Recommended Citation Lewis, Lily Roberta, "Resolving Amphitropical Phylogeographic Histories in the Common Dung Moss Tetraplodon (Bryopsida: Splachnaceae)." (2015). Doctoral Dissertations. 747. https://opencommons.uconn.edu/dissertations/747 Resolving Amphitropical Phylogeographic Histories in the Common Dung Moss Tetraplodon (Bryopsida: Splachnaceae). Lily Roberta Lewis, PhD University of Connecticut, 2015 Many plants have geographic disjunctions, with one of the more rare, yet extreme being the amphitropical, or bipolar disjunction. Bryophytes (namely mosses and liverworts) exhibit this pattern more frequently relative to other groups of plants and typically at or below the level of species. The processes that have shaped the amphitropical disjunction have been infrequently investigated, with notably a near absence of studies focusing on mosses. This dissertation explores the amphitropical disjunction in the dung moss Tetraplodon, with a special emphasis on the origin of the southernmost South American endemic T. fuegianus. Chapter 1 delimits three major lineages within Tetraplodon with distinct yet overlapping geographic ranges, including an amphitropical lineage containing the southernmost South American endemic T. fuegianus. Based on molecular divergence date estimation and phylogenetic topology, the American amphitropical disjunction is traced to a single direct long-distance dispersal event across the tropics. Chapter 2 provides the first evidence supporting the role of migratory shore birds in dispersing bryophytes, as well as other plant, fungal, and algal diaspores across the tropics. -
Occurrence of the Green Shield-Moss Buxbaumia Viridis (Moug.) Brid
Article Occurrence of the Green Shield-Moss Buxbaumia viridis (Moug.) Brid. in the Bieszczady Mountains of Poland Piotr Brewczy ´nski 1, Kamil Grałek 2 and Piotr Bila ´nski 3,* 1 Głogów Forest District, ul. Fabryczna 57, 36-060 Głogów Małopolski, Poland; [email protected] 2 The Regional Directorate of the State Forests in Krosno, ul. Bieszczadzka 2, 38-400 Krosno, Poland; [email protected] 3 Department of Forest Ecosystems Protection, University of Agriculture in Krakow, Al. 29 Listopada 46, 31-425 Krakow, Poland * Correspondence: [email protected]; Tel.: +48-1266-253-69 Abstract: The small-sized gametophytes and sporophytes of the green shield-moss Buxbaumia viridis (Moug.) Brid. make it difficult to study. However, in Europe, there has been increasing interest in this species in the past few years, mostly as a result of the implementation of the Natura 2000 network. In Poland, B. viridis has only been reported in isolated studies that have been limited in terms of area and the number of participating workers. One of the Polish regions where B. viridis was recently recorded is the Bieszczady Mountains, but there have been no large-scale surveys of that region to date. The objective of the current work was to describe the B. viridis population in the Bieszczady Mountains in terms of its spatial distribution and abundance, investigate its selected microhabitat preferences, and evaluate the conservation status of this moss species within the Natura 2000 site Bieszczady PLC180001. The studied region encompassed 93,490.44 ha, including 69,056.23 ha of managed forests and 24,434.21 ha of forests belonging to the Bieszczady National Park. -
The Ulota Crispa Group in Britain and Ireland, with Notes on Other Species of the Genus
Article The Ulota crispa group in Britain and Ireland Diagnostic characters in the genus Ulota In other species the base is only weakly concave The Ulota crispa group in and it narrows gradually to the lamina (Fig. 3). 1. Leaves This character is important in separating the Leaf characters are of limited value in identifying species of the U. crispa group. The first type Britain and Ireland, with notes Ulota species, but with two notable exceptions. (concave and abruptly narrowed) is found in U. crispa s.str. and U. intermedia, the second type 1.1 Marginal leaf cells above the base. In Ulota in U. crispula. However the difference is not on other species of the genus calvescens there is a band of elongate cells inside always completely clear-cut, and in such cases it the margin of the leaf that reaches some distance is important to check several mature leaves from Tom Blockeel introduces some newly recognised species of Ulota and above the base, up to mid-leaf or thereabouts more than one shoot. discusses the identification of species in this fascinating genus when well-developed (Fig. 1). It varies in its development from leaf to leaf, even on different lota crispa has been a problematic species a variable species, but recently bryologists in sides of the same leaf, but is always distinct and since the earliest days of European Spain have studied it in detail, using both obvious in most leaves. Among our other Ulota bryology. In Britain and Ireland the morphological and molecular techniques. They species, only U. -
A Synopsis of the Genus Cryphaea Mohr & Weber (Cryphaeaceae, Bryopsida)
81,9(56,7<2)+(/6,1., Department of Ecology and Systematics Division of Systematic Biology FINLAND 0RQRJUDSKLFVWXGLHVRQ&U\SKDHD %U\RSVLGD 3(1*&+(1*5$2 $FDGHPLFGLVVHUWDWLRQ 7REHSUHVHQWHGZLWKWKHSHUPLVVLRQRIWKH)DFXOW\RI6FLHQFHRIWKH8QLYHUVLW\RI+HOVLQNL IRUSXEOLFFULWLFLVPLQWKH$XGLWRULXPRIWKH'HSDUWPHQWRI(FRORJ\DQG6\VWHPDWLFV 8QLRQLQNDWX+HOVLQNL 2Q'HFDWR¶FORFN Helsinki 2001 This thesis comprises A synopsis of the genus &U\SKDHD (Cryphaeaceae, Bryopsida). — published in %U\REURWKHUD 7: 1–35, 2001 And the author’s publications upon which the synopsis is largely based: 1. Rao, P. & Enroth, J. 1999. Taxonomic studies on &U\SKDHD (Cryphaeaceae, Bryopsida). 1. The Chinese species and notes on &\SWRGRQWRSVLV. — %U\REURWKHUD 5: 177–188 (QRW LQFOXGHGKHUH). 2. Rao, P. 2000. Taxonomic studies on &U\SKDHD (Cryphaeaceae, Bryopsida). 2. Revision of Asian species. — $QQ%RW)HQQLFL 37: 45–56 (QRWLQFOXGHGKHUH). 3. Rao, P. 2001. Taxonomic studies on &U\SKDHD (Cryphaeaceae, Bryopsida). 3. Revision of European, African, Australian and Oceanian, and American species. — %U\REURWKHUD7: 37–111 (QRWLQFOXGHGKHUH). ISBN 952-10-0248-4 (PDF) http://ethesis.helsinki.fi ISSN 1235-3949 ISBN 951-98893-0-2 (nid.) Helsinki 2001 2 $V\QRSVLVRIWKHJHQXV&U\SKDHD &U\SKDHDFHDH%U\RSVLGD Pengcheng Rao Rao, P., Department of Ecology and Systematics, Division of Systematic Biology, P. O. Box 47, FIN-00014 University of Helsinki, Finland The genus &U\SKDHD (Cryphaeaceae, Bryopsida) comprises 30 species including two new species described from China after revisions. Twenty-three specific or infraspecific names were reduced to synonymy. The taxonomic status of five species was changed and the necessary new combinations were made. Twenty-five names were lectotypified or neotypified. The identities of five specific epithets remain unknown because no type material was found. -
New Taxonomical Arrangement of the Traditionally Conceived Genera Orthotrichum and Ulota (Orthotrichaceae, Bryophyta)
ISSN 2336-3193 Acta Mus. Siles. Sci. Natur., 64: 169-174, 2015 DOI: 10.1515/cszma-2015-0024 New taxonomical arrangement of the traditionally conceived genera Orthotrichum and Ulota (Orthotrichaceae, Bryophyta) Vítězslav Plášek, Jakub Sawicki, Ryszard Ochyra, Monika Szczecińska & Tomasz Kulik New taxonomical arrangement of the traditionally conceived genera Orthotrichum and Ulota (Orthotrichaceae, Bryophyta). – Acta Mus. Siles. Sci. Natur., 64: 169-174, 2015. Abstract: The traditionally conceived genera Orthotrichum Hedw. and Ulota F.Weber are here reclassified into six genera, Orthotrichum, Dorcadion Lindb., Nyholmiella Holmen & E.Warncke, Pulvigera Plášek, Sawicki & Ochyra, Plenogemma Plášek, Sawicki & Ochyra, and Ulota, based on morphological differences and partially on molecular evidence. The genus Pulvigera includes P. lyellii (Hook. & Taylor) Plášek, Sawicki & Ochyra (Orthotrichum lyellii Hook. & Taylor) which was selected as its generitype. The genus Plenogemma includes P. phyllantha (Brid.) Plášek, Sawicki & Ochyra (Ulota phyllantha Brid.) which was selected as its generitype. Key words: Orthotrichum; Dorcadion; Nyholmiella; Plenogemma gen. nov.; Pulvigera gen. nov.; Ulota; moss taxonomy Introduction Orthotrichum Hedw. is a cosmopolitan moss genus consisting of 159 species (Sawicki, Plášek & Szczecińska 2012) and it is the second largest genus in the family Orthotrichaceae. Taxonomic subdivision within this genus has been the subject of continued debate since the late 19th century. Certain taxa were repeatedly included in or removed from the genus Orthotrichum in an attempt to better clarify infrageneric taxa, including subgenera and sections. The history of taxonomic classification of the genus Orthotrichum has been described in detail by Lewinsky (1993) and Lewinsky-Haapasaari and Hedenäs (1998). A phylogenetic analysis revealed the polyphyletic nature of the genus (Goffinet, Bayer & Vitt 1998; Goffinet et al. -
Phytochrome Diversity in Green Plants and the Origin of Canonical Plant Phytochromes
ARTICLE Received 25 Feb 2015 | Accepted 19 Jun 2015 | Published 28 Jul 2015 DOI: 10.1038/ncomms8852 OPEN Phytochrome diversity in green plants and the origin of canonical plant phytochromes Fay-Wei Li1, Michael Melkonian2, Carl J. Rothfels3, Juan Carlos Villarreal4, Dennis W. Stevenson5, Sean W. Graham6, Gane Ka-Shu Wong7,8,9, Kathleen M. Pryer1 & Sarah Mathews10,w Phytochromes are red/far-red photoreceptors that play essential roles in diverse plant morphogenetic and physiological responses to light. Despite their functional significance, phytochrome diversity and evolution across photosynthetic eukaryotes remain poorly understood. Using newly available transcriptomic and genomic data we show that canonical plant phytochromes originated in a common ancestor of streptophytes (charophyte algae and land plants). Phytochromes in charophyte algae are structurally diverse, including canonical and non-canonical forms, whereas in land plants, phytochrome structure is highly conserved. Liverworts, hornworts and Selaginella apparently possess a single phytochrome, whereas independent gene duplications occurred within mosses, lycopods, ferns and seed plants, leading to diverse phytochrome families in these clades. Surprisingly, the phytochrome portions of algal and land plant neochromes, a chimera of phytochrome and phototropin, appear to share a common origin. Our results reveal novel phytochrome clades and establish the basis for understanding phytochrome functional evolution in land plants and their algal relatives. 1 Department of Biology, Duke University, Durham, North Carolina 27708, USA. 2 Botany Department, Cologne Biocenter, University of Cologne, 50674 Cologne, Germany. 3 University Herbarium and Department of Integrative Biology, University of California, Berkeley, California 94720, USA. 4 Royal Botanic Gardens Edinburgh, Edinburgh EH3 5LR, UK. 5 New York Botanical Garden, Bronx, New York 10458, USA. -
Table 3B: Status Category Summary by Major Taxonomic Group (Plants)
IUCN Red List version 2019-2: Table 3b Last updated: 18 July 2019 Table 3b: Status category summary by major taxonomic group (plants) Subtotal** Subtotal Subtotal Class* EX EW CR(PE)** CR(PEW)** (EX+EW+ CR EN VU NT LR/cd DD LC Total (EX+EW) (threatened spp.) CR(PE)+CR(PEW)) ANDREAEOPSIDA 0 0 0 0 0 0 0 0 1 1 0 0 1 0 2 ANTHOCEROTOPSIDA 0 0 0 0 0 0 0 2 0 2 0 0 0 0 2 BRYOPSIDA 4 0 4 0 0 4 24 36 33 93 22 0 17 35 171 CHAROPHYACEAE 0 0 0 0 0 0 0 0 0 0 0 0 3 8 11 CHLOROPHYCEAE 0 0 0 0 0 0 0 0 0 0 0 0 1 0 1 CYCADOPSIDA 0 4 4 1 3 8 53 65 74 192 63 0 3 45 307 FLORIDEOPHYCEAE 1 0 1 2 0 3 6 0 3 9 0 0 44 4 58 GINKGOOPSIDA 0 0 0 0 0 0 0 1 0 1 0 0 0 0 1 GNETOPSIDA 0 0 0 0 0 0 0 1 3 4 7 0 10 76 97 JUNGERMANNIOPSIDA 0 0 0 0 0 0 12 23 20 55 10 0 2 18 85 LILIOPSIDA 9 4 13 64 2 79 532 901 809 2,242 390 10 688 2,715 6,058 LYCOPODIOPSIDA 0 0 0 2 0 2 14 11 16 41 9 0 8 31 89 MAGNOLIOPSIDA 107 26 133 170 18 321 2,292 3,843 5,159 11,294 1,458 170 1,579 10,926 25,560 MARCHANTIOPSIDA 0 0 0 0 0 0 2 3 1 6 1 0 4 1 12 PINOPSIDA 0 0 0 1 0 1 29 96 79 204 98 0 7 298 607 POLYPODIOPSIDA 2 1 3 8 0 11 62 70 79 211 27 0 54 209 504 POLYTRICHOPSIDA 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 SPHAGNOPSIDA 0 0 0 0 0 0 1 1 2 4 0 0 0 1 5 TAKAKIOPSIDA 0 0 0 0 0 0 0 0 1 1 0 0 0 0 1 ULVOPHYCEAE 0 0 0 0 0 0 0 0 0 0 0 0 1 0 1 Total 123 35 158 248 23 429 3,027 5,053 6,279 14,359 2,086 180 2,420 14,367 33,570 IUCN Red List Categories: EX - Extinct, EW - Extinct in the Wild, CR - Critically Endangered (includes CR(PE) and CR(PEW)), EN - Endangered, VU - Vulnerable, LR/cd - Lower Risk/conservation dependent, NT - Near Threatened (includes LR/nt - Lower Risk/near threatened), DD - Data Deficient, LC - Least Concern (includes LR/lc - Lower Risk, least concern).