Neckeraceae, Bryophyta) from Northern Vietnam
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Floristic Study of Bryophytes in a Subtropical Forest of Nabeup-Ri at Aewol Gotjawal, Jejudo Island
− pISSN 1225-8318 Korean J. Pl. Taxon. 48(1): 100 108 (2018) eISSN 2466-1546 https://doi.org/10.11110/kjpt.2018.48.1.100 Korean Journal of ORIGINAL ARTICLE Plant Taxonomy Floristic study of bryophytes in a subtropical forest of Nabeup-ri at Aewol Gotjawal, Jejudo Island Eun-Young YIM* and Hwa-Ja HYUN Warm Temperate and Subtropical Forest Research Center, National Institute of Forest Science, Seogwipo 63582, Korea (Received 24 February 2018; Revised 26 March 2018; Accepted 29 March 2018) ABSTRACT: This study presents a survey of bryophytes in a subtropical forest of Nabeup-ri, known as Geumsan Park, located at Aewol Gotjawal in the northwestern part of Jejudo Island, Korea. A total of 63 taxa belonging to Bryophyta (22 families 37 genera 44 species), Marchantiophyta (7 families 11 genera 18 species), and Antho- cerotophyta (1 family 1 genus 1 species) were determined, and the liverwort index was 30.2%. The predominant life form was the mat form. The rates of bryophytes dominating in mesic to hygric sites were higher than the bryophytes mainly observed in xeric habitats. These values indicate that such forests are widespread in this study area. Moreover, the rock was the substrate type, which plays a major role in providing micro-habitats for bryophytes. We suggest that more detailed studies of the bryophyte flora should be conducted on a regional scale to provide basic data for selecting indicator species of Gotjawal and evergreen broad-leaved forests on Jejudo Island. Keywords: bryophyte, Aewol Gotjawal, liverwort index, life-form Jejudo Island was formed by volcanic activities and has geological, ecological, and cultural aspects (Jeong et al., 2013; unique topological and geological features. -
Economic and Ethnic Uses of Bryophytes
Economic and Ethnic Uses of Bryophytes Janice M. Glime Introduction Several attempts have been made to persuade geologists to use bryophytes for mineral prospecting. A general lack of commercial value, small size, and R. R. Brooks (1972) recommended bryophytes as guides inconspicuous place in the ecosystem have made the to mineralization, and D. C. Smith (1976) subsequently bryophytes appear to be of no use to most people. found good correlation between metal distribution in However, Stone Age people living in what is now mosses and that of stream sediments. Smith felt that Germany once collected the moss Neckera crispa bryophytes could solve three difficulties that are often (G. Grosse-Brauckmann 1979). Other scattered bits of associated with stream sediment sampling: shortage of evidence suggest a variety of uses by various cultures sediments, shortage of water for wet sieving, and shortage around the world (J. M. Glime and D. Saxena 1991). of time for adequate sampling of areas with difficult Now, contemporary plant scientists are considering access. By using bryophytes as mineral concentrators, bryophytes as sources of genes for modifying crop plants samples from numerous small streams in an area could to withstand the physiological stresses of the modern be pooled to provide sufficient material for analysis. world. This is ironic since numerous secondary compounds Subsequently, H. T. Shacklette (1984) suggested using make bryophytes unpalatable to most discriminating tastes, bryophytes for aquatic prospecting. With the exception and their nutritional value is questionable. of copper mosses (K. G. Limpricht [1885–]1890–1903, vol. 3), there is little evidence of there being good species to serve as indicators for specific minerals. -
Volatile Concentrate from the Neotropical Moss Neckeropsis Undulata (Hedw.) Reichardt, Existing in the Brazilian Amazon Thyago G
Miranda et al. BMC Chemistry (2021) 15:7 https://doi.org/10.1186/s13065-021-00736-3 BMC Chemistry RESEARCH ARTICLE Open Access Volatile concentrate from the neotropical moss Neckeropsis undulata (Hedw.) Reichardt, existing in the brazilian Amazon Thyago G. Miranda1, Raynon Joel M. Alves1, Ronilson F. de Souza2, José Guilherme S. Maia3, Pablo Luis B. Figueiredo2* and Ana Cláudia C. Tavares‑Martins1,2 Abstract Background: Many natural compounds have been identifed and synthesized by the advancement of bryophytes phytochemistry studies. This work aimed to report the composition of Neckeropsis undulata (Hedw.) Reichardt moss volatiles, sampled in the Combú Island, Belém city, Pará state, Brazil. The volatile concentrate of N. undulata was obtained by a simultaneous distillation‑extraction micro‑system, analyzed by GC and GC‑MS, and reported for the frst time. Results: Ten compounds were identifed in the volatile concentrate, corresponding to 91.6% of the total, being 1‑octen‑3‑ol (35.7%), α‑muurolol (21.4%), naphthalene (11.3%), and n‑hexanal (10.0 %) the main constituents. Most of the constituents of the N. undulata volatile concentrate have been previously identifed in other mosses, and liver‑ worts spread wide in the world. Conclusions: 1‑Octen‑3‑ol, n‑hexanal, 2‑ethylhexanol, isoamyl propionate, and octan‑3‑one are already known metabolic products obtained from enzymatic oxidation of polyunsaturated fatty acids, belonging to the large family of minor oxygenated compounds known as oxylipins. The knowledge of the composition of volatiles from moss N. undulata could contribute to the Neckeraceae species’ chemotaxonomy. Keywords: Neckeraceae, Volatile concentrate, 1‑octen‑3‑ol, α‑muurolol, n‑hexanal Background Brazil’s bryophyte fora comprises 1524 species, of which Bryophytes are small terrestrial spore-forming green 880 are mosses, 633 liverworts, and 11 hornworts. -
Flora of New Zealand Mosses
FLORA OF NEW ZEALAND MOSSES BRACHYTHECIACEAE A.J. FIFE Fascicle 46 – JUNE 2020 © Landcare Research New Zealand Limited 2020. Unless indicated otherwise for specific items, this copyright work is licensed under the Creative Commons Attribution 4.0 International licence Attribution if redistributing to the public without adaptation: "Source: Manaaki Whenua – Landcare Research" Attribution if making an adaptation or derivative work: "Sourced from Manaaki Whenua – Landcare Research" See Image Information for copyright and licence details for images. CATALOGUING IN PUBLICATION Fife, Allan J. (Allan James), 1951- Flora of New Zealand : mosses. Fascicle 46, Brachytheciaceae / Allan J. Fife. -- Lincoln, N.Z. : Manaaki Whenua Press, 2020. 1 online resource ISBN 978-0-947525-65-1 (pdf) ISBN 978-0-478-34747-0 (set) 1. Mosses -- New Zealand -- Identification. I. Title. II. Manaaki Whenua-Landcare Research New Zealand Ltd. UDC 582.345.16(931) DC 588.20993 DOI: 10.7931/w15y-gz43 This work should be cited as: Fife, A.J. 2020: Brachytheciaceae. In: Smissen, R.; Wilton, A.D. Flora of New Zealand – Mosses. Fascicle 46. Manaaki Whenua Press, Lincoln. http://dx.doi.org/10.7931/w15y-gz43 Date submitted: 9 May 2019 ; Date accepted: 15 Aug 2019 Cover image: Eurhynchium asperipes, habit with capsule, moist. Drawn by Rebecca Wagstaff from A.J. Fife 6828, CHR 449024. Contents Introduction..............................................................................................................................................1 Typification...............................................................................................................................................1 -
Molecular Phylogeny of Chinese Thuidiaceae with Emphasis on Thuidium and Pelekium
Molecular Phylogeny of Chinese Thuidiaceae with emphasis on Thuidium and Pelekium QI-YING, CAI1, 2, BI-CAI, GUAN2, GANG, GE2, YAN-MING, FANG 1 1 College of Biology and the Environment, Nanjing Forestry University, Nanjing 210037, China. 2 College of Life Science, Nanchang University, 330031 Nanchang, China. E-mail: [email protected] Abstract We present molecular phylogenetic investigation of Thuidiaceae, especially on Thudium and Pelekium. Three chloroplast sequences (trnL-F, rps4, and atpB-rbcL) and one nuclear sequence (ITS) were analyzed. Data partitions were analyzed separately and in combination by employing MP (maximum parsimony) and Bayesian methods. The influence of data conflict in combined analyses was further explored by two methods: the incongruence length difference (ILD) test and the partition addition bootstrap alteration approach (PABA). Based on the results, ITS 1& 2 had crucial effect in phylogenetic reconstruction in this study, and more chloroplast sequences should be combinated into the analyses since their stability for reconstructing within genus of pleurocarpous mosses. We supported that Helodiaceae including Actinothuidium, Bryochenea, and Helodium still attributed to Thuidiaceae, and the monophyletic Thuidiaceae s. lat. should also include several genera (or species) from Leskeaceae such as Haplocladium and Leskea. In the Thuidiaceae, Thuidium and Pelekium were resolved as two monophyletic groups separately. The results from molecular phylogeny were supported by the crucial morphological characters in Thuidiaceae s. lat., Thuidium and Pelekium. Key words: Thuidiaceae, Thuidium, Pelekium, molecular phylogeny, cpDNA, ITS, PABA approach Introduction Pleurocarpous mosses consist of around 5000 species that are defined by the presence of lateral perichaetia along the gametophyte stems. Monophyletic pleurocarpous mosses were resolved as three orders: Ptychomniales, Hypnales, and Hookeriales (Shaw et al. -
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. -
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………………………………………………………… -
Neckera Inopinata (Neckeraceae, Bryophyta), a New Species from Hunan and Zhejiang, China
Polish Botanical Journal 57(1): 63–68, 2012 NECKERA INOPINATA (NECKERACEAE, BRYOPHYTA), A NEW SPECIES FROM HUNAN AND ZHEJIANG, CHINA JOHANNES ENROTH Abstract. Neckera inopinata Enroth (Neckeraceae) is described as a new species from Hunan Province and Zhejiang Province, China. It can be distinguished by the following suite of characters: plants of relatively small stature; leaves variably undulate, shortly decurrent, ovate-lingulate to ovate; costa reaching to midleaf or above; leaf margins very sharply serrulate; and upper laminal cells solid-walled. An identifi cation key to the species of Neckera s.l. in China is provided. Key words: moss fl ora of China, new species, taxonomy, morphology Johannes Enroth, Department of Biosciences and Botanical Museum, P.O. Box 7, FI-00014 University of Helsinki, Finland; e-mail: johannes.enroth@helsinki.fi INTRODUCTION As a result of recent phylogenetic analyses based 2011). Those changes were not included in the on several genomic regions (Olsson et al. 2009a, most recently published treatment of the Chinese b, 2010, 2011), the taxonomy and systematics of Neckera by Wu (2011), who recognized a total the moss family Neckeraceae have undergone of 17 species, neglecting some recently described profound modifi cations at all taxonomic levels. ones (Ji & Miao 2009; Enroth & Ji 2010), as well The family circumscription and generic con- as some that were recently reported for the fi rst tent have changed, and some of the traditional time for China (Ji & Enroth 2010). Wu (2011) genera have been split into smaller genera. One did not treat N. complanata at all, although it has of those traditional (and heterogeneous) group- been reported from Shaanxi Province and Shanxi ings is Neckera Hedw., which was divided into Province (cf. -
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..................................................................................................... -
Phylogeny of Neckeropsis and Himantocladium (Neckeraceae, Bryophytina)
Bry. Div. Evo. 38 (2): 053–070 ISSN 2381-9677 (print edition) DIVERSITY & http://www.mapress.com/j/bde BRYOPHYTE EVOLUTION Copyright © 2016 Magnolia Press Article ISSN 2381-9685 (online edition) http://dx.doi.org/10.11646/bde.38.2.4 Phylogeny of Neckeropsis and Himantocladium (Neckeraceae, Bryophytina) SANNA OLSSON1,2*, JOHANNES ENROTH3*, SANNA HUTTUNEN4 & DIETMAR QUANDT5 1Department of Agricultural Sciences, University of Helsinki, P.O. Box 27, FI-00014 Helsinki, Finland 2INIA Forest Research Centre (INIA-CIFOR), Dept. Forest Ecology and Genetics, Carretera de A Coruña km 7.5, E-28040 Madrid, Spain 3Department of Biological and Environmental Sciences and Botanical Museum, University of Helsinki, P.O. Box 7, FI-00014 Helsinki, Finland 4Department of Biology, FI-20014 University of Turku, Finland 5Nees-Institute for Biodiversity of Plants, University of Bonn, Meckenheimer Allee 170, 53115 Bonn, Germany *Corresponding author: Sanna Olsson, e-mail: [email protected], tel.: +34634509635 or Johannes Enroth, e-mail: Johannes. [email protected], tel.:+3580294157792 Abstract Two closely related tropical genera from the pleurocarpous moss family Neckeraceae are revised: the second largest genus in the family, Neckeropsis, currently with 29 species, and Himantocladium, comprising six species. Twenty-one species of Neckeropsis and five of Himantocladium were included in this study, which is based on phylogenetic analyses using sequence level data from the plastid (rps4)-trnT-trnL-trnF cluster and rpl16 as well as nuclear ITS1 & 2. Neckeropsis ap- peared as polyphyletic. Neckeropsis s. str. comprises 12 species and a further four species, not included in the analysis, are tentatively retained in the genus based on morphology. -
Household and Personal Uses
Glime, J. M. 2017. Household and Personal Uses. Chapt. 1-1. In: Glime, J. M. Bryophyte Ecology. Volume 5. Uses. Ebook sponsored 1-1-1 by Michigan Technological University and the International Association of Bryologists. Last updated 5 October 2017 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology/>. CHAPTER 1 HOUSEHOLD AND PERSONAL USES TABLE OF CONTENTS Household Uses...................................................................................................................................................1-1-2 Furnishings...................................................................................................................................................1-1-4 Padding and Absorption...............................................................................................................................1-1-5 Mattresses.............................................................................................................................................1-1-6 Shower Mat...........................................................................................................................................1-1-7 Urinal Absorption.................................................................................................................................1-1-8 Cleaning.......................................................................................................................................................1-1-8 Brushes and Brooms.............................................................................................................................1-1-8 -
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THAMNOBRYUM Josephine Milne1 & Niels Klazenga2 Thamnobryum Nieuwl., Amer. Midl. Naturalist 5: 50 (1917); from the Greek thamnos (a bush or shrub) and bryon (a moss), in reference to bush-like habit of these mosses. Type: T. alopecurum (Hedw.) Gangulee Diocious. Plants small or robust, frondose, forming wefts or dense mats. Primary stem creeping; fronds irregularly pinnate to bipinnate, terete-foliate to strongly complanate, with attenuate to flagelliform tips; central strand absent. Stipe leaves erecto-patent to patent, triangular; basal part occasionally appressed; margin entire; costa broad. Frond axis leaves spirally arranged to subdistichous, erecto-patent, elliptical to ovate, smooth to plicate; apex obtuse to short-acuminate, sometimes apiculate; margin entire below, crenulate or serrate near the apex; costa single and strong, reaching mid-leaf or to just below apex. Laminal cells occasionally thick-walled; upper laminal cells irregularly quadrate to rhomboidal; median cells slightly elongate; basal cells linear. Branch leaves similar but smaller. Perichaetia and perigonia in leaf axils of frond axes and branches. Calyptra cucullate. Capsules long-exserted, inclined to horizontal, cylindrical; stomata at the base of the capsule, phaneropore; annulus differentiated; operculum rostrate, oblique. Peristome: exostome teeth triangular, the tips hyaline and the outer face with a distinct median zig-zag line, densely horizontally striate below, papillose above; endostome with a high basal membrane; processes gaping at the base, papillose; cilia 2 or 3, papillose. Spores globose, smooth or slightly papillose. Thamnobryum is a genus of 20–30 species with an almost cosmopolitan distribution. It is most diverse in the Old World, and it is represented in Australia by three species.