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Revision and Checklist of the Moss Families Bartramiaceae and Mniaceae in Vietnam Timo KOPONEN1, Thanh-Luc NGUYEN2, Thien-Tam L
Hattoria 10: 69–107. 2019 Revision and checklist of the moss families Bartramiaceae and Mniaceae in Vietnam Timo KOPONEN1, Thanh-Luc NGUYEN2, Thien-Tam LUONG3, 4 & Sanna HUTTUNEN4 1 Finnish-Chinese Botanical Foundation, Mailantie 109, FI-08800 Lohja, Finland & Finnish Museum of Natural History, Botany Unit (bryology), P.O. Box 7 (Unioninkatu 4), FI-00014 University of Helsinki, Finland 2 Southern Institute of Ecology, Vietnam Academy of Science and Technology, 1 Mac Dinh Chi, District 1, Ho Chi Minh City, Vietnam 3 University of Science, Vietnam National University Ho Chi Minh City, 227 Nguyen Van Cu, District 5, Ho Chi Minh City, Vietnam 4 Herbarium (TUR), Biodiversity Unit, FI 20014 University of Turku, Finland Author for correspondence: Thanh-Luc NGUYEN, [email protected] Abstract The genera Fleischerobryum Loeske and Philonotis Brid. of the Bartramiaceae and the family Mniaceae (excluding Pohlia Hedw.) are revised for Vietnam, based on specimens studied and literature reports. Four species are added to the flora: Orthomnion javense (M.Fleisch.) T.J.Kop., Philonotis asperifolia Mitt., P. laii T.J.Kop., P. speciosa (Griff.) Mitt. syn. nov. (based on P. mercieri Paris & Broth.), and Plagiomnium wui (T.J.Kop.) Y.J.Yi & S.He. Eight species are excluded from the flora. Two taxa are considered doubtful. The flora now includes one species of Fleischerobryum, eight species of Philonotis, one species of Mnium Hedw. (doubtful), three species of Orthomnion Wills. and five species of Plagiomnium (one doubtful). The 15 species are divided into phytogeographical elements. Eight belong to the Southeast Asiatic temperate to meridional element, and seven to the Southeast Asiatic meridional to subtropical element. -
Monoicous Species Pairs in the Mniaceae (Bryophyta); Morphology, Sexual Condition and Distiribution
ISSN 2336-3193 Acta Mus. Siles. Sci. Natur., 68: 67-81, 2019 DOI: 10.2478/cszma-2019-0008 Published: online 1 July 2019, print July 2019 On the hypothesis of dioicous − monoicous species pairs in the Mniaceae (Bryophyta); morphology, sexual condition and distiribution Timo Koponen On the hypothesis of dioicous − monoicous species pairs in the Mniaceae (Bryophyta); morphology, sexual condition and distiribution. – Acta Mus. Siles. Sci. Natur., 68: 67-81, 2019. Abstract: Some early observations seemed to show that, in the Mniaceae, the doubling of the chromo- some set affects a change from dioicous to monoicous condition, larger size of the gametophyte including larger leaf cell size, and to a wider range of the monoicous counterpart. The Mniaceae taxa are divided into four groups based on their sexual condition and morphology. 1. Dioicous – monoicous counterparts which can be distinguished by morphological characters, 2. Dioicous – monoicous taxa which have no morphological, deviating characters, 3. Monoicous species mostly with diploid chromosome number for which no dioicous counterpart is known, and 4. The taxa in Mniaceae with only dioicous plants. Most of the monoicous species of the Mniaceae have wide ranges, but a few of them are endemics in geographically isolated areas. The dioicous species have either a wide holarctic range or a limited range in the forested areas of temperate and meridional North America, Europe and SE Asia, or in subtropical Asia. Some of the monoicous species are evidently autodiploids and a few of them are allopolyploids from cross-sections of two species. Quite recently, several new possible dioicous – monoicous relationships have been discovered. -
Bryoflora of the Great Cypress Swamp Conservation Area, Sussex County, Delaware and Worcester County, Maryland
The Maryland Naturalist 43 (3-4):9-17 . July/December 1999 The Bryoflora of the Great Cypress Swamp Conservation Area, Sussex County, Delaware and Worcester County, Maryland William A. McAvoy Introduction In 1998 the Delaware Natural Heritage Program (DNHP), with funding from the U.S. Environmental Protection Agency, completed a biological/ecological survey of the Great Cypress Swamp Conservation Area (GCSCA). The GCSCA is located in the central portion of the Delmarva Peninsula (a land area composed of the coastal plain counties of Delaware and the eastern shore counties of Maryland and Virginia) and lies on the border of Sussex County, Delaware and Worcester County, Maryland (Figure 1). Though the survey included a variety of inventories (avian, amphibian and reptile, natural community, and rare vascular plants), it is the data collected on bryophytes (mosses and liverworts) that are reported here. The study ofbryophytes on the Delmarva Peninsula has attracted very little interest over the years, and a search of the literature revealed only four pertinent papers. Owens (1949), while studying at the University of Maryland, submitted a graduate thesis titled A Preliminary List of Maryland Mosses and their Distribution. This annotated list, containing county distribution data and briefhabitat notes, included 198 taxa of mosses for the state of Maryland, with 65 taxa attributed to the eastern shore counties of Delmarva. Owens's list was based solely on pre-I 949 collections at US and MARY (Herbaria acronyms follow Holmgren et al. 1990). Confirmations and determinations were made by the author, as well as by numerous other authorities in the field ofbryology (Owens 1949). -
The Use of Dna Barcoding to Address Major Taxonomic Problems for Rare British Bryophytes
THE USE OF DNA BARCODING TO ADDRESS MAJOR TAXONOMIC PROBLEMS FOR RARE BRITISH BRYOPHYTES FINAL REVISED REPORT FEBRUARY 2013 David Bell David Long Pete Hollingsworth Royal Botanic Garden Edinburgh With major contribution from D.T. Holyoak (Bryum) CONTENTS 1. Executive summary……………………………………………………………… 3 2. Introduction……………………………………………………………………… 4 3. Methods 3.1 Sampling……………………………………………………………….. 6 3.2 DNA extraction & sequencing…………………………………………. 7 3.3 Data analysis…………………………………………………………… 9 4. Results 4.1 Sequencing success…………………………………………………….. 9 4.2 Species accounts 4.2.1 Atrichum angustatum ………………………………………… 10 4.2.2 Barbilophozia kunzeana ………………………………………13 4.2.3 Bryum spp……………………………………………………. 16 4.2.4 Cephaloziella spp…………………………………………….. 26 4.2.5 Ceratodon conicus …………………………………………… 29 4.2.6 Ditrichum cornubicum & D. plumbicola …………………….. 32 4.2.7 Ephemerum cohaerens ……………………………………….. 36 4.2.8 Eurhynchiastrum pulchellum ………………………………… 36 4.2.9 Leiocolea rutheana …………………………………………... 39 4.2.10 Marsupella profunda ……………………………………….. 42 4.2.11 Orthotrichum pallens & O. pumilum ……………………….. 45 4.2.12 Pallavicinia lyellii …………………………………………... 48 4.2.13 Rhytidiadelphus subpinnatus ……………………………….. 49 4.2.14 Riccia bifurca & R. canaliculata ………………………........ 51 4.2.15 Sphaerocarpos texanus ……………………………………... 54 4.2.16 Sphagnum balticum ………………………………………… 57 4.2.17 Thamnobryum angustifolium & T. cataractarum …………... 60 4.2.18 Tortula freibergii …………………………………………… 62 5. Conclusions……………………………………………………………………… 65 6. Dissemination of results………………………………………………………… -
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..................................................................................................... -
Tardigrade Reproduction and Food
Glime, J. M. 2017. Tardigrade Reproduction and Food. Chapt. 5-2. In: Glime, J. M. Bryophyte Ecology. Volume 2. Bryological 5-2-1 Interaction. Ebook sponsored by Michigan Technological University and the International Association of Bryologists. Last updated 18 July 2020 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology2/>. CHAPTER 5-2 TARDIGRADE REPRODUCTION AND FOOD TABLE OF CONTENTS Life Cycle and Reproductive Strategies .............................................................................................................. 5-2-2 Reproductive Strategies and Habitat ............................................................................................................ 5-2-3 Eggs ............................................................................................................................................................. 5-2-3 Molting ......................................................................................................................................................... 5-2-7 Cyclomorphosis ........................................................................................................................................... 5-2-7 Bryophytes as Food Reservoirs ........................................................................................................................... 5-2-8 Role in Food Web ...................................................................................................................................... 5-2-12 Summary .......................................................................................................................................................... -
Species List For: Labarque Creek CA 750 Species Jefferson County Date Participants Location 4/19/2006 Nels Holmberg Plant Survey
Species List for: LaBarque Creek CA 750 Species Jefferson County Date Participants Location 4/19/2006 Nels Holmberg Plant Survey 5/15/2006 Nels Holmberg Plant Survey 5/16/2006 Nels Holmberg, George Yatskievych, and Rex Plant Survey Hill 5/22/2006 Nels Holmberg and WGNSS Botany Group Plant Survey 5/6/2006 Nels Holmberg Plant Survey Multiple Visits Nels Holmberg, John Atwood and Others LaBarque Creek Watershed - Bryophytes Bryophte List compiled by Nels Holmberg Multiple Visits Nels Holmberg and Many WGNSS and MONPS LaBarque Creek Watershed - Vascular Plants visits from 2005 to 2016 Vascular Plant List compiled by Nels Holmberg Species Name (Synonym) Common Name Family COFC COFW Acalypha monococca (A. gracilescens var. monococca) one-seeded mercury Euphorbiaceae 3 5 Acalypha rhomboidea rhombic copperleaf Euphorbiaceae 1 3 Acalypha virginica Virginia copperleaf Euphorbiaceae 2 3 Acer negundo var. undetermined box elder Sapindaceae 1 0 Acer rubrum var. undetermined red maple Sapindaceae 5 0 Acer saccharinum silver maple Sapindaceae 2 -3 Acer saccharum var. undetermined sugar maple Sapindaceae 5 3 Achillea millefolium yarrow Asteraceae/Anthemideae 1 3 Actaea pachypoda white baneberry Ranunculaceae 8 5 Adiantum pedatum var. pedatum northern maidenhair fern Pteridaceae Fern/Ally 6 1 Agalinis gattingeri (Gerardia) rough-stemmed gerardia Orobanchaceae 7 5 Agalinis tenuifolia (Gerardia, A. tenuifolia var. common gerardia Orobanchaceae 4 -3 macrophylla) Ageratina altissima var. altissima (Eupatorium rugosum) white snakeroot Asteraceae/Eupatorieae 2 3 Agrimonia parviflora swamp agrimony Rosaceae 5 -1 Agrimonia pubescens downy agrimony Rosaceae 4 5 Agrimonia rostellata woodland agrimony Rosaceae 4 3 Agrostis elliottiana awned bent grass Poaceae/Aveneae 3 5 * Agrostis gigantea redtop Poaceae/Aveneae 0 -3 Agrostis perennans upland bent Poaceae/Aveneae 3 1 Allium canadense var. -
New Dihydrobiflavones from the Moss Plagiomnium Cuspidatum
New Dihydrobiflavones from the Moss Plagiomnium cuspidatum Siegbert Anhut, Tassilo Seeger, H.-Dietmar Zinsmeister FB 15, Botanik, Universität des Saarlandes, D-6600 Saarbrücken, Bundesrepublik Deutschland Hans Geiger Institut für Chemie der Universität Hohenheim, D-7000 Stuttgart 70, Bundesrepublik Deutschland Z. Naturforsch. 44c, 189—192 (1989); received November 25, 1988 Mosses, Mniaceae, Plagiomnium cuspidatum. Dihydrobiflavone In Plagiomnium cuspidatum the three new dihydrobiflavones 2,3-dihydro-5'-hydroxyamento- flavone, 2,3-dihydro-5',3'"-dihydroxyamentoflavone and 2,3-dihydro-5'-hydroxyrobustaflavone were detected. Introduction For a long time 5',8"-biluteolin (= 5',3'"-di- hydroxyamentoflavone) from Dicranum scoparium [ 1 , 2 ] was the only known biflavonoid in bryophytes. Meanwhile this compound and other biflavonoids have been isolated from other mosses [3—6]. Most recently we described the isolation of a luteolin-apigenin dimer, 5'-hydroxyamentoflavone, from Plagiomnium elatum [3]. In continuation of the Amentoflavone (4) R = R' = H chemical investigation of the moss family Mniaceae 5',3"'-Dihydroxyamentoflavone (5) R = R' = OH the biflavonoids of Plagiomnium cuspidatum were ( = 5',8"-Biluteolin) studied. Results and Discussion From Plagiomnium cuspidatum three biflavonoids 2, 3, 7 were isolated. By 'H NMR studies, however, it was obvious that 2 contains additionally a small amount of the further compound 8 . Robustaflavone (6) R = R' H 5',3'"-Dihydroxyrobustaflavone ( 7 ) R = R' OH (= 5',6"-Biluteolin) OH 0 ,3-Dihydroamentoflavone (1) R = R' = H ,3-Dihydro-5'-hydroxyamentoflavone (2) R = OH, R' = H ,3-Dihydro-5',3'"-dihydroxyamentoflavone (3) R = R' = OH Reprint requests to Prof. Dr. Zinsmeister. Verlag der Zeitschrift für Naturforschung, D-7400 Tübingen 0341 - 0382/89/0300- 0189 $01.30/0 2,3-Dihydro-5'-hydroxyrobustaflavone (8) 190 S. -
The IUCN Red List of Threatened Speciestm
Species 2014 Annual ReportSpecies the Species of 2014 Survival Commission and the Global Species Programme Species ISSUE 56 2014 Annual Report of the Species Survival Commission and the Global Species Programme • 2014 Spotlight on High-level Interventions IUCN SSC • IUCN Red List at 50 • Specialist Group Reports Ethiopian Wolf (Canis simensis), Endangered. © Martin Harvey Muhammad Yazid Muhammad © Amazing Species: Bleeding Toad The Bleeding Toad, Leptophryne cruentata, is listed as Critically Endangered on The IUCN Red List of Threatened SpeciesTM. It is endemic to West Java, Indonesia, specifically around Mount Gede, Mount Pangaro and south of Sukabumi. The Bleeding Toad’s scientific name, cruentata, is from the Latin word meaning “bleeding” because of the frog’s overall reddish-purple appearance and blood-red and yellow marbling on its back. Geographical range The population declined drastically after the eruption of Mount Galunggung in 1987. It is Knowledge believed that other declining factors may be habitat alteration, loss, and fragmentation. Experts Although the lethal chytrid fungus, responsible for devastating declines (and possible Get Involved extinctions) in amphibian populations globally, has not been recorded in this area, the sudden decline in a creekside population is reminiscent of declines in similar amphibian species due to the presence of this pathogen. Only one individual Bleeding Toad was sighted from 1990 to 2003. Part of the range of Bleeding Toad is located in Gunung Gede Pangrango National Park. Future conservation actions should include population surveys and possible captive breeding plans. The production of the IUCN Red List of Threatened Species™ is made possible through the IUCN Red List Partnership. -
2780 Y.-J. Yoon Et Al
2780 Y.-J. Yoon et al. Mitochondrial DNA Part A, 2016; 27(4): 2779–2780 Family Order Class Treubia lacunosa Treubiaceae Treubiales 100/100 Marchantia polymorpha Marchantiaceae Marchantiales Marchantiopsida 100/87 Pleurozia purpurea Pleuroziaceae Pleuroziales Sphagnum palustre Sphagnaceae Sphagnales Sphagnopsida 57/100 Tetraphis pellucida Tetraphidaceae Tetraphidales 100/100 Atrichum angustatum Polytrichaceae Polytrichales Polytrichopsida Buxbaumia aphylla Buxbaumiaceae Buxbaumiales 100/100 100/100 Physcomitrella patens Funariaceae Funariales 100/* Funaria hygrometrica Syntrichia filaris Pottiaceae Pottiales 98/79 100/100 Codriophorus laevigatus 100/100 Grimmiaceae Grimmiales Racomitrium ericoides 87/* Bartramia pomiformis Bartramiaceae Bryales Orthotrichum stellatum 100/100 Bryopsida 100/100 Orthotrichum speciosum Orthotrichaceae Orthotrichales 92/94 Ulota hutchinsiae 99/99 Ptychomnion cygnisetum Ptychomniaceae Ptychomniales 100/100 Climacium americanum Climaciaceae 100/100 Hypnum imponens Hypnaceae Hypnales */53 Anomodon rugelii Anomodontaceae 100/100/ Anomodon attenuatus 100 Figure 1. Phylogenetic position of Syntrichia filaris determined by Maximum Parsimony analysis based on combined analysis with amino acids sequences of 31 mitochondrial genes common in all taxa. The bootstrap values (450) are presented near the corresponding branch (ML/MP). Branches that were supported by above 70 % bootstrap values are indicated by bold lines. Sequences from Marchantiopsida were used as outgroup. GenBank accession numbers of mitogenomes used are -
Field Guide to the Moss Genera in New Jersey by Keith Bowman
Field Guide to the Moss Genera in New Jersey With Coefficient of Conservation and Indicator Status Keith Bowman, PhD 10/20/2017 Acknowledgements There are many individuals that have been essential to this project. Dr. Eric Karlin compiled the initial annotated list of New Jersey moss taxa. Second, I would like to recognize the contributions of the many northeastern bryologists that aided in the development of the initial coefficient of conservation values included in this guide including Dr. Richard Andrus, Dr. Barbara Andreas, Dr. Terry O’Brien, Dr. Scott Schuette, and Dr. Sean Robinson. I would also like to acknowledge the valuable photographic contributions from Kathleen S. Walz, Dr. Robert Klips, and Dr. Michael Lüth. Funding for this project was provided by the United States Environmental Protection Agency, Region 2, State Wetlands Protection Development Grant, Section 104(B)(3); CFDA No. 66.461, CD97225809. Recommended Citation: Bowman, Keith. 2017. Field Guide to the Moss Genera in New Jersey With Coefficient of Conservation and Indicator Status. New Jersey Department of Environmental Protection, New Jersey Forest Service, Office of Natural Lands Management, Trenton, NJ, 08625. Submitted to United States Environmental Protection Agency, Region 2, State Wetlands Protection Development Grant, Section 104(B)(3); CFDA No. 66.461, CD97225809. i Table of Contents Introduction .................................................................................................................................................. 1 Descriptions -
Establishment and Development of the Catherine’S Moss Atrichum Undulatum (Hedw.) P
Arch. Biol. Sci., Belgrade, 58 (2), 87-93, 2006. ESTABLISHMENT AND DEVELOPMENT OF THE CATHERINE’S MOSS ATRICHUM UNDULATUM (HEDW.) P. BEAUV. (POLYTRICHACEAE) IN IN VITRO CONDITIONS 1 ANETA SABOVLJEVIĆ1, 2, TIJANACVETIĆ andM. SABOVLJEVIĆ1, 3 1Institute of Botany and Botanical Garden, Faculty of Biology, University of Belgrade, 11000 Belgrade, Serbia and Montenegro 2Institute of Botany, University of Cologne, 50931 Cologne, Germany 3AG Bryology, Nees Institute of Botany, University of Bonn, 53115 Bonn, Germany Abstract - The effect of sucrose and mineral salts on morphogenesis of the Catherine’s moss (Atrichum undulatum)in in vitro culture was tested. In vitro culture of this species was established from disinfected spores on Murashige and Skoog (MS) medium. Apical shoots of gametophytes were used to investigate the influence of sucrose and mineral salts on protonemal and gametophyte growth and multiplication. Paper also treats morpho-anatomical characteristics of plants grown in nature and plants derived from in vitro culture. Key words: Brzophytes, morphogenesis, Catherine’s moss, growth, multiplication UDC 582.325.1:57.08 INTRODUCTION higher plants, (2) haploid gametophyte of the dominant vegetative phase, and (3) lower chromosome numbers The Catherine’s moss [Atrichum undulatum (Hedw.) P. (Gang et al., 2003). Cells of bryophytes, especially in Beauv.] is among the largest European terrestrial moss suspension culture, have been noted as ideal materials for species. It is widespread across Europe, and due to its morphogenetic, genetic, physiological, biochemical, and size is widely used in moss biology research (e.g., Be- molecular studies (O n o et al., 1988). querel, 1906; G e m m e l l, 1953; W o r d, 1960; Sitte, 1963; W o l t e r s, 1964; B r o w n and Lem- According to F e l i x (1994), 31 liverworts, 18 mon, 1987; O n o et al., 1987; L i n d e m a n n et al., mosses, and one hornwort have been used asexperimen- 1989; M i l e s and L o n g t o n, 1990; Stoneburn- tal objects in the sterile culture of bryophytes.