A Diversity Account of Bryaceae (Bryophyta: Musci) of Nepal
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A Revised Red List of Bryophytes in Britain
ConservationNews Revised Red List distinguished from Extinct. This Red List uses Extinct in the Wild (EW) – a taxon is Extinct version 3.1 of the categories and criteria (IUCN, in the Wild when it is known to survive only in A revised Red List of 2001), along with guidelines produced to assist cultivation or as a naturalized population well with their interpretation and use (IUCN, 2006, outside the past range. There are no taxa in this 2008), further guidelines for using the system category in the British bryophyte flora. bryophytes in Britain at a regional level (IUCN, 2003), and specific Regionally Extinct (RE) – a taxon is regarded guidelines for applying the system to bryophytes as Regionally Extinct in Britain if there are no (Hallingbäck et al., 1995). post-1979 records and all known localities have Conservation OfficerNick Hodgetts presents the latest revised Red List for How these categories and criteria have been been visited and surveyed without success, or interpreted and applied to the British bryophyte if colonies recorded post-1979 are known to bryophytes in Britain. Dumortiera hirsuta in north Cornwall. Ian Atherton flora is summarized below, but anyone interested have disappeared. It should be appreciated that in looking into them in more depth should regional ‘extinction’ for bryophytes is sometimes he first published Red List of et al. (2001) and Preston (2010), varieties and consult the original IUCN documents, which less final than for other, more conspicuous bryophytes in Britain was produced subspecies have been disregarded. are available on the IUCN website (www. organisms. This may be because bryophytes are in 2001 as part of a Red Data Book 1980 has been chosen as the cut-off year to iucnredlist.org/technical-documents/categories- easily overlooked, or because their very efficient for bryophytes (Church et al., 2001). -
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………………………………………………………… -
Part 2 – Fruticose Species
Appendix 5.2-1 Vegetation Technical Appendix APPENDIX 5.2‐1 Vegetation Technical Appendix Contents Section Page Ecological Land Classification ............................................................................................................ A5.2‐1‐1 Geodatabase Development .............................................................................................. A5.2‐1‐1 Vegetation Community Mapping ..................................................................................... A5.2‐1‐1 Quality Assurance and Quality Control ............................................................................ A5.2‐1‐3 Limitations of Ecological Land Classification .................................................................... A5.2‐1‐3 Field Data Collection ......................................................................................................... A5.2‐1‐3 Supplementary Results ..................................................................................................... A5.2‐1‐4 Rare Vegetation Species and Rare Ecological Communities ........................................................... A5.2‐1‐10 Supplementary Desktop Results ..................................................................................... A5.2‐1‐10 Field Methods ................................................................................................................. A5.2‐1‐16 Supplementary Results ................................................................................................... A5.2‐1‐17 Weed Species -
Notes on Bryaceae (Bryopsida) in Japan
Hattoria 5: 51-70, 2014 Notes on Bryaceae (Bryopsida) in Japan Tadashi Suzuki1 1The Hattori Botanical Laboratory, Shimada Branch, 6480-3 Takasago-cho, Shimada-shi, Shizuoka- ken 427-0054, Japan Abstract. Four genera of Bryaceae, Acidodontium Schwaegr., Orthodontium Schwaegr., Pseudopohlia Williams and Schizymenium Harv. are newly found in Japan. Two species of Acidodontium, A. megalocarpum (Hook.) Ren. & Card. and A. longifolium (Par.) Broth., two species of Orthodontium, O. denticulatum Geh. & Hampe and O. pellucens (Hook.) Bruch, Schimp. & Gümbel, Pseudopohlia didymodontia (Mitt.) A. L. Andrews, Schizymenium novoguinense (E. B. Bartram) A. Eddy, three species of Brachymenium, B. alpinum Ochi, B. jilinense T. J. Kop., A. J. Shaw, J.-S. Lou & C. Gao and B. muricola Broth. and Mielichhoferia pusilla (Hook. f. & Wilson) Mitt. are added to the moss flora of Japan. Two new combinations, Schizymenium japonicum (Besch.) Tad. Suzuki and Schizymenium sasaokae (Broth.) Tad. Suzuki are made. Introduction In a catalog of the mosses of Japan, Iwatsuki (2004) listed 9 genera of Bryaceae. In this paper, four genera of Bryaceae are added to the moss flora of Japan and I present information on 12 species of the family in Japan. A key to genera of Bryaceae in Japan is provided. Descriptions, specimens examined, distributions, notes and illustrations of 12 species are included. All collections are deposited in the Herbarium of the Hattori Botanical Laboratory (NICH). Key to genera of Bryaceae in Japan 1. Upper leaf cells linear-rhomboidal, firm-walled, basal leaf cells abruptly short-rectangular to subquadrate; axillary gemmae present ·························································· Pseudopohlia 1. Plants not with combination of characters mentioned above ·················································· 2 2. -
Annotated Checklist of Estonian Bryophytes
Folia Cryptog. Estonica, Fasc. 52: 109–127 (2015) http://dx.doi.org/10.12697/fce.2015.52.14 Annotated checklist of Estonian bryophytes Kai Vellak1,2, Nele Ingerpuu2, Mare Leis3 & Loore Ehrlich4 1Natural History Museum, University of Tartu, 46 Vanemuise Street, Tartu 51014. E-mail: [email protected] 2Institute of Ecology and Earth Sciences, University of Tartu, 40 Lai Street, Tartu 51005. E-mail: [email protected] 3Institute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, 5 Fr. R. Kreutzwald Street, 51014 Tartu. E-mail: [email protected] 4Estonian Museum of Natural History, 26 Toompuiestee Street, 10148 Tallinn. E-mail: [email protected] Abstract: The updated list of Estonian bryophytes includes 594 species from all three phyla. Only one species is reported for Estonia according to the literature data, all others have voucher speciemens in herbaria, two of them outside of Estonia. Altogether 242 species are frequent in Estonia, 173 species are rare, and 161 are sporadically distributed. We do not have any recent data for 20 species, and their presence in Estonia is doubtful. In 2008 a new Estonian Red list was compiled and 369 bryophyte species were evaluated against IUCN criteria. Approximately one fifth of the Estonian bryoflora (129 species) is designated to the three threat categories. Keywords: Bryoflora, frequencies of species, protected species, red list INTRODUCTION The diversity of taxa at the global or local scale taxa according to recently accepted synonyms, depends greatly on the taxonomical research. supply every taxa with a voucher specimen, The species number of bryophytes in the world estimate the present frequency in Estonia and varies between 15 000 and 20 000 (Shaw et al., give proper names in Estonian for new taxa or 2011). -
This Is the Published Version of a Paper Published in Ecology. Citation for the Original Published Pa
http://www.diva-portal.org This is the published version of a paper published in Ecology. Citation for the original published paper (version of record): Dynesius, M., Hylander, K., Nilsson, C. (2009) High resilience of bryophyte assemblages in stream-side compared to upland forests. Ecology, 90: 1042-1054 http://dx.doi.org/10.1890/07-1822.1 Access to the published version may require subscription. N.B. When citing this work, cite the original published paper. Permanent link to this version: http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-20912 Ecology, 90(4), 2009, pp. 1042–1054 Ó 2009 by the Ecological Society of America High resilience of bryophyte assemblages in streamside compared to upland forests 1,3 2 1 MATS DYNESIUS, KRISTOFFER HYLANDER, AND CHRISTER NILSSON 1Landscape Ecology Group, Department of Ecology and Environmental Science, Umea˚ University, SE-901 87 Umea˚, Sweden 2Department of Botany, Stockholm University, 106 91 Stockholm, Sweden Abstract. Landscape heterogeneity causes spatial variation in disturbance regimes and resilience. We asked whether the resilience of bryophyte (liverwort and moss) assemblages to clear-cutting differs between streamside and upland boreal forests in northern Sweden. We hypothesized that bryophyte survival and recolonization rates are higher in streamside areas, thus raising resilience. Conversely, disturbance-intolerant but also invading species should be more frequent here, potentially reducing resilience. In each of 18 sites, we compared two 0.1-ha plots (one streamside and one upland) located in old forest that had never been clear-cut with two matching plots in young stands established after clear-cutting of old forests 30–50 years earlier. -
Liverworts, Mosses and Hornworts of Afghanistan - Our Present Knowledge
ISSN 2336-3193 Acta Mus. Siles. Sci. Natur., 68: 11-24, 2019 DOI: 10.2478/cszma-2019-0002 Published: online 1 July 2019, print July 2019 Liverworts, mosses and hornworts of Afghanistan - our present knowledge Harald Kürschner & Wolfgang Frey Liverworts, mosses and hornworts of Afghanistan ‒ our present knowledge. – Acta Mus. Siles. Sci. Natur., 68: 11-24, 2019. Abstract: A new bryophyte checklist for Afghanistan is presented, including all published records since the beginning of collection activities in 1839 ‒1840 by W. Griffith till present. Considering several unidentified collections in various herbaria, 23 new records for Afghanistan together with the collection data can be added to the flora. Beside a new genus, Asterella , the new records include Amblystegium serpens var. serpens, Brachythecium erythrorrhizon, Bryum dichotomum, B. elwendicum, B. pallens, B. weigelii, Dichodontium palustre, Didymodon luridus, D. tectorum, Distichium inclinatum, Entosthodon muhlenbergii, Hygroamblystegium fluviatile subsp. fluviatile, Oncophorus virens, Orthotrichum rupestre var. sturmii, Pogonatum urnigerum, Pseudocrossidium revolutum, Pterygoneurum ovatum, Schistidium rivulare, Syntrichia handelii, Tortella inflexa, T. tortuosa, and Tortula muralis subsp. obtusifolia . Therewith the number of species increase to 24 liverworts, 246 mosses and one hornwort. In addition, a historical overview of the country's exploration and a full biogeography of Afghan bryophytes is given. Key words: Bryophytes, checklist, flora, phytodiversity. Introduction Recording, documentation, identification and classification of organisms is a primary tool and essential step in plant sciences and ecology to obtain detailed knowledge on the flora of a country. In many countries, such as Afghanistan, however, our knowledge on plant diversity, function, interactions of species and number of species in ecosystems is very limited and far from being complete. -
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 -
The Genus Anomobryum Schimp. (Bryopsida, Bryaceae) in Australia
777 The genus Anomobryum Schimp. (Bryopsida, Bryaceae) in Australia John R. Spence and Helen P. Ramsay Abstract Spence, John R.1 and Ramsay, Helen P.2 (1National Park Service, Glen Canyon NRA, PO Box 1507, Page, AZ 86040, USA; 2National Herbarium of New South Wales, Mrs. Macquaries Road, Royal Botanic Gardens, Sydney, NSW 2000, Australia) 2002. The genus Anomobryum Schimp. (Bryopsida, Bryaceae) in Australia. Telopea 9(4) 777–792. The genus Anomobryum has been revised for Australia and five species are recognized: A. auratum (Mitt.) A. Jaeger, A. harriottii (R. Br. bis.) Dixon, Anomobryum sp. (= Bryum argenteum Hedw.), and two new combinations made for species transferred from Bryum: A. lanatum (P. Beauv.) J.R. Spence & H.P. Ramsay, and A. subrotundifolium (A. Jaeger) J.R. Spence & H.P. Ramsay. Keys, descriptions, illustrations and distributions are presented for the species in Australia. Relationships with other genera in the Bryaceae are discussed. Introduction In this study the genus Anomobryum (Bryaceae) has been examined in detail as a contribution for the Flora of Australia. Anomobryum is closely related to the widespread genus Bryum and most bryologists (e.g. Smith 1978, Crum & Anderson 1981, Noguchi 1994, Eddy 1996) consider it a separate genus, although Ochi (1970, 1992) retained it as a subgenus within Bryum. In general Anomobryum is distinguished by its very small size, julaceous stems, and leaves with a weak costa and smooth margins, all features that it shares with the silver Bryum species, such as B. argenteum Hedw. At least two species of Anomobryum are also silver in colouration like B. argenteum and its allies. -
Bryophyte Flora of the Czech Republic: Updated Checklist and Red List and a Brief Analysis
Preslia 84: 813–850, 2012 813 Bryophyte flora of the Czech Republic: updated checklist and Red List and a brief analysis Bryoflóra České republiky: aktualizace seznamu a červeného seznamu a stručná analýza Dedicated to the centenary of the Czech Botanical Society (1912–2012) Jan K u č e r a1, Jiří Vá ň a2 & Zbyněk H r a d í l e k3 1University of South Bohemia, Faculty of Science, Branišovská 31, CZ–370 05 České Budějovice, Czech Republic, e-mail: [email protected]; 2Charles University Prague, Department of Botany, Faculty of Science, Benátská 2, CZ–128 01 Prague 2, Czech Republic, e-mail: [email protected]; 3Palacký University Olomouc, Department of Botany, Faculty of Science, Šlechtitelů 11, CZ-783 71 Olomouc-Holice, Czech Republic, e-mail: [email protected]. Kučera J., Váňa J. & Hradílek Z. (2012): Bryophyte flora of the Czech Republic: updated checklist and Red List and a brief analysis. – Preslia 84: 813–850. The bryoflora of the Czech Republic is analysed using an updated version of the checklist that includes recent taxonomic and nomenclatural changes. In addition, the baseline data was com- pletely revised using the IUCN 3.1 criteria. The main list includes 863 species of bryophytes (4 hornworts, 207 liverworts and 652 mosses) with 5 additional subspecies and 23 generally recog- nized varieties; 9 additional species are listed as of doubtful taxonomic status and 17 other species are evaluated as of uncertain occurrence. Of the 892 taxa evaluated, 46% qualified for inclusion in Red List categories (40 taxa in category RE, 70 in CR, 88 in EN, 93 in VU, 66 in LR-nt, 24 in DD-va and 30 in DD), while 54% are considered Least Concern (LC). -
An All-Taxa Biodiversity Inventory of the Huron Mountain Club
AN ALL-TAXA BIODIVERSITY INVENTORY OF THE HURON MOUNTAIN CLUB Version: August 2016 Cite as: Woods, K.D. (Compiler). 2016. An all-taxa biodiversity inventory of the Huron Mountain Club. Version August 2016. Occasional papers of the Huron Mountain Wildlife Foundation, No. 5. [http://www.hmwf.org/species_list.php] Introduction and general compilation by: Kerry D. Woods Natural Sciences Bennington College Bennington VT 05201 Kingdom Fungi compiled by: Dana L. Richter School of Forest Resources and Environmental Science Michigan Technological University Houghton, MI 49931 DEDICATION This project is dedicated to Dr. William R. Manierre, who is responsible, directly and indirectly, for documenting a large proportion of the taxa listed here. Table of Contents INTRODUCTION 5 SOURCES 7 DOMAIN BACTERIA 11 KINGDOM MONERA 11 DOMAIN EUCARYA 13 KINGDOM EUGLENOZOA 13 KINGDOM RHODOPHYTA 13 KINGDOM DINOFLAGELLATA 14 KINGDOM XANTHOPHYTA 15 KINGDOM CHRYSOPHYTA 15 KINGDOM CHROMISTA 16 KINGDOM VIRIDAEPLANTAE 17 Phylum CHLOROPHYTA 18 Phylum BRYOPHYTA 20 Phylum MARCHANTIOPHYTA 27 Phylum ANTHOCEROTOPHYTA 29 Phylum LYCOPODIOPHYTA 30 Phylum EQUISETOPHYTA 31 Phylum POLYPODIOPHYTA 31 Phylum PINOPHYTA 32 Phylum MAGNOLIOPHYTA 32 Class Magnoliopsida 32 Class Liliopsida 44 KINGDOM FUNGI 50 Phylum DEUTEROMYCOTA 50 Phylum CHYTRIDIOMYCOTA 51 Phylum ZYGOMYCOTA 52 Phylum ASCOMYCOTA 52 Phylum BASIDIOMYCOTA 53 LICHENS 68 KINGDOM ANIMALIA 75 Phylum ANNELIDA 76 Phylum MOLLUSCA 77 Phylum ARTHROPODA 79 Class Insecta 80 Order Ephemeroptera 81 Order Odonata 83 Order Orthoptera 85 Order Coleoptera 88 Order Hymenoptera 96 Class Arachnida 110 Phylum CHORDATA 111 Class Actinopterygii 112 Class Amphibia 114 Class Reptilia 115 Class Aves 115 Class Mammalia 121 INTRODUCTION No complete species inventory exists for any area. -
Arctic Biodiversity Assessment
310 Arctic Biodiversity Assessment Purple saxifrage Saxifraga oppositifolia is a very common plant in poorly vegetated areas all over the high Arctic. It even grows on Kaffeklubben Island in N Greenland, at 83°40’ N, the most northerly plant locality in the world. It is one of the first plants to flower in spring and serves as the territorial flower of Nunavut in Canada. Zackenberg 2003. Photo: Erik Thomsen. 311 Chapter 9 Plants Lead Authors Fred J.A. Daniëls, Lynn J. Gillespie and Michel Poulin Contributing Authors Olga M. Afonina, Inger Greve Alsos, Mora Aronsson, Helga Bültmann, Stefanie Ickert-Bond, Nadya A. Konstantinova, Connie Lovejoy, Henry Väre and Kristine Bakke Westergaard Contents Summary ..............................................................312 9.4. Algae ..............................................................339 9.1. Introduction ......................................................313 9.4.1. Major algal groups ..........................................341 9.4.2. Arctic algal taxonomic diversity and regionality ..............342 9.2. Vascular plants ....................................................314 9.4.2.1. Russia ...............................................343 9.2.1. Taxonomic categories and species groups ....................314 9.4.2.2. Svalbard ............................................344 9.2.2. The Arctic territory and its subdivision .......................315 9.4.2.3. Greenland ...........................................344 9.2.3. The flora of the Arctic ........................................316