Cypripedium Botanical Investigation
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On Tropical Drosera Rotundifolia L
Technical Refereed Contribution On tropical Drosera rotundifolia L. Andreas Fleischmann • Botanische Staatssammlung München and GeoBio-Center LMU University • Menzinger Strasse 67 • D-80638 Munich • Germany • [email protected] Abstract: Two aspects on the morphology and biology of the Philippine population of D. rotundifo- lia were not answered by Coritico and Fleischmann (2016), namely its seed morphology and sea- sonal growth cycle - especially regarding hibernaculum formation, as it is known from its temperate congeners. These gaps can now be covered from observations made from cultivated plants and shall be reported here. Further aspects on the biology of Philippine D. rotundifolia (and other tropical populations of temperate Drosera) in cultivation and natural habitat are presented. Distribution and altitudinal range of Drosera rotundifolia The generic type species of Drosera, Drosera rotundifolia L., is probably the most well-known sundew species, at least to people from the Northern Hemisphere. It is also the most widespread1, its range spans the entire boreal region (Fig. 1; Meusel et al. 1965). Its southernmost populations in the Northern Hemisphere are situated in SE China, in the mountain ranges of northern Guangdong province, at ca. 24.5°N (Coritico & Fleischmann 2016). In Europe its more or less continuous range reaches to ca. 39°N to the south in central Spain, in North America to ca. 34°N in northern Georgia and Alabama states, in Japan to 30°N on the island of Yakushima (Coritico & Fleischmann 2016). Additionally, D. rotundifolia shows a few isolated outlier populations in some areas of the Mediter- ranean [e.g. on the isle of Corsica, France (Delange & Hugot 2020), in the Sierra Nevada of southern Spain (Lorite 2016), and in northern Greece (just three sites known in the Rhodope Mountains; The- odoropoulos & Eleftheriadou 2012)], in central Lebanon (Diels 1906; Tohmé & Tohmé 2007; despite erroneous claims, e.g. -
Vegetative Ecology of a Montane Mire, Crater Lake National
AJ ABSTRACT OF THE THESIS OF Susan Cornelia Seyer for the degree of Master of Science in Botany and Plant Pathology presented on December 14, 1979 Title: VEGETATIVE ECOLOGY OF A MONTANE MIRE, CRATER LAKE NATIONAL PARK, OREGON Redacted for Privacy Abstract approved: Jerry F. Franklin Mires, or peat-producing ecosystems, dominated by sedges, shrubs, and brown mosses, are common features in Cascade subalpine regions, occurring where moisture accumulates in small basins or on poorly-drained slopes. Although descriptions and classifications have been developed for mire vegetation in much of the world, there is little information of even a descriptive nature for these montane mires in Oregon and Washington. This thesis reports on phytosocia- logical structure, env'ironental relations, and successional trends in one such mire in the Oregon Cascade mountains. To characterize the general phytosociological structure of the mire vegetation at Sphagnum Bog, Crater Lake National Park, quantitative species cover data were used in conjunction with a Braun-Blanquet tabular analysis and two-dimensional stand ordinations, reciprocal averaging and a Bray-Curtis polar ordination. Defined community types correspond to physiognomic types as follows: Carex rostrata (reedswamp); Eleocharis pauciflora-Carex limosa, Eleocharis pauciflora/bryophytes (low sedge fens); Carex sichensis (tall sedge fen); Vaccinium/ Aulacomnium palustre, Vaccinium occidentala/Carex sitchensis (shrub thickets; Alnus incana/Brachythacium sp. and Salix barclayi (marginal carrs).Phases were defined when appropriate. A vegetation map was made to illustrate the locations and extent of the variouscommunities. Comparisons with other montane mires in thearea determined that the physiognomic units defined are repeatable when appropriate habitat conditions are present, and that they usually includemany of the same characteristic species, the dominant mosses being particularly constant. -
State of New York City's Plants 2018
STATE OF NEW YORK CITY’S PLANTS 2018 Daniel Atha & Brian Boom © 2018 The New York Botanical Garden All rights reserved ISBN 978-0-89327-955-4 Center for Conservation Strategy The New York Botanical Garden 2900 Southern Boulevard Bronx, NY 10458 All photos NYBG staff Citation: Atha, D. and B. Boom. 2018. State of New York City’s Plants 2018. Center for Conservation Strategy. The New York Botanical Garden, Bronx, NY. 132 pp. STATE OF NEW YORK CITY’S PLANTS 2018 4 EXECUTIVE SUMMARY 6 INTRODUCTION 10 DOCUMENTING THE CITY’S PLANTS 10 The Flora of New York City 11 Rare Species 14 Focus on Specific Area 16 Botanical Spectacle: Summer Snow 18 CITIZEN SCIENCE 20 THREATS TO THE CITY’S PLANTS 24 NEW YORK STATE PROHIBITED AND REGULATED INVASIVE SPECIES FOUND IN NEW YORK CITY 26 LOOKING AHEAD 27 CONTRIBUTORS AND ACKNOWLEGMENTS 30 LITERATURE CITED 31 APPENDIX Checklist of the Spontaneous Vascular Plants of New York City 32 Ferns and Fern Allies 35 Gymnosperms 36 Nymphaeales and Magnoliids 37 Monocots 67 Dicots 3 EXECUTIVE SUMMARY This report, State of New York City’s Plants 2018, is the first rankings of rare, threatened, endangered, and extinct species of what is envisioned by the Center for Conservation Strategy known from New York City, and based on this compilation of The New York Botanical Garden as annual updates thirteen percent of the City’s flora is imperiled or extinct in New summarizing the status of the spontaneous plant species of the York City. five boroughs of New York City. This year’s report deals with the City’s vascular plants (ferns and fern allies, gymnosperms, We have begun the process of assessing conservation status and flowering plants), but in the future it is planned to phase in at the local level for all species. -
Fossil Mosses: What Do They Tell Us About Moss Evolution?
Bry. Div. Evo. 043 (1): 072–097 ISSN 2381-9677 (print edition) DIVERSITY & https://www.mapress.com/j/bde BRYOPHYTEEVOLUTION Copyright © 2021 Magnolia Press Article ISSN 2381-9685 (online edition) https://doi.org/10.11646/bde.43.1.7 Fossil mosses: What do they tell us about moss evolution? MicHAEL S. IGNATOV1,2 & ELENA V. MASLOVA3 1 Tsitsin Main Botanical Garden of the Russian Academy of Sciences, Moscow, Russia 2 Faculty of Biology, Lomonosov Moscow State University, Moscow, Russia 3 Belgorod State University, Pobedy Square, 85, Belgorod, 308015 Russia �[email protected], https://orcid.org/0000-0003-1520-042X * author for correspondence: �[email protected], https://orcid.org/0000-0001-6096-6315 Abstract The moss fossil records from the Paleozoic age to the Eocene epoch are reviewed and their putative relationships to extant moss groups discussed. The incomplete preservation and lack of key characters that could define the position of an ancient moss in modern classification remain the problem. Carboniferous records are still impossible to refer to any of the modern moss taxa. Numerous Permian protosphagnalean mosses possess traits that are absent in any extant group and they are therefore treated here as an extinct lineage, whose descendants, if any remain, cannot be recognized among contemporary taxa. Non-protosphagnalean Permian mosses were also fairly diverse, representing morphotypes comparable with Dicranidae and acrocarpous Bryidae, although unequivocal representatives of these subclasses are known only since Cretaceous and Jurassic. Even though Sphagnales is one of two oldest lineages separated from the main trunk of moss phylogenetic tree, it appears in fossil state regularly only since Late Cretaceous, ca. -
2.10 Meesia Longiseta HEDW. Code: 1389 Anhang: II
2.10 Meesia longiseta HEDW. Code: 1389 Anhang: II KLAUS WEDDELING, GERHARD LUDWIG & MONIKA HACHTEL, Bonn Namen: D: Langstieliges Schwanenhalsmoos, Langstieliges Meesemoos, Gestreckte Langborste E: Long-stalked Thread Moss, Long-shafted Swan Moss, F: – Systematik/Taxonomie: Bryophyta, Bryopsida, Bryidae, Splachnales, Meesiaceae. Synonyme: Amblyodon longisetus (HEDW.) P. BEAUV. Kennzeichen/Artbestimmung: Meesia longiseta ist ein 4–8 (–10) cm hohes, akrokarpes, unverzweigtes Laubmoos von grün-schwärzlicher Färbung. Die Art wächst in lockeren, weichen Rasen (Abb. 2.9). Das Stämmchen ist bis in die Spitze wurzelhaarig und im Moose Querschnitt dreikantig. Die Blättchen sind mehr oder weniger deutlich in 3 oder 6 Rei- hen angeordnet und vom Stämmchen abgespreizt. Die 2–3,5 mm langen, spitzen Blätt- chen laufen deutlich am Stämmchen herab, sind oberwärts gekielt, ganzrandig oder an der Spitze etwas gezähnt. Ihre deutlich entwickelte Rippe endet unterhalb der Blattspitze. Der Blattrand ist flach. Die Laminazellen sind rechteckig bis rhombisch und etwa 14 µm breit. Die rötlichen, gedrehten Seten der synözischen Art können über 10 cm lang wer- den. Die langbirnenförmige, aufrechte Kapsel hat einen deutlichen Hals. Bei der Spo- renreife im Juni und Juli werden die mit 36–44 µm Durchmesser recht großen Sporen frei- gesetzt. Die Chromosomenzahl ist nicht bekannt (FRITSCH 1991). Differenzierende Merkmale zu den ähnlichen Arten Meesia uliginosa und M. hexasticha sind der nicht ein- gerollte Blattrand, die kleineren Sporen und der Rippenquerschnitt mit kleinen, inneren Zellen (zusammengestellt nach CRUM & ANDERSON 1981, FRAHM 1979, LIMPRICHT 1895). Abbildungen der Art finden sich bei CRUM & ANDERSON (1981, Fig. 296, 297, S. 628, 629: Blättchen, Blattspitze, Habitus, Kapsel) und FRAHM (1979, Fig. -
Moss Occurrences in Yugyd Va National Park, Subpolar and Northern Urals, European North-East Russia
Biodiversity Data Journal 7: e32307 doi: 10.3897/BDJ.7.e32307 Data Paper Moss occurrences in Yugyd Va National Park, Subpolar and Northern Urals, European North-East Russia Galina Zheleznova‡, Tatyana Shubina‡, Svetlana Degteva‡‡, Ivan Chadin , Mikhail Rubtsov‡ ‡ Institute of Biology of Komi Scientific Centre of the Ural Branch of the Russian Academy of Sciences, Syktyvkar, Russia Corresponding author: Tatyana Shubina ([email protected]) Academic editor: Yasen Mutafchiev Received: 10 Dec 2018 | Accepted: 25 Mar 2019 | Published: 01 Apr 2019 Citation: Zheleznova G, Shubina T, Degteva S, Chadin I, Rubtsov M (2019) Moss occurrences in Yugyd Va National Park, Subpolar and Northern Urals, European North-East Russia. Biodiversity Data Journal 7: e32307. https://doi.org/10.3897/BDJ.7.e32307 Abstract Background This study produced a dataset containing information on moss occurrences in the territory of Yugyd Va National Park, located in the Subpolar and Northern Urals, European North- East Russia. The dataset summarises occurrences noted by long-term bryological explorations in remote areas of the Subpolar and Northern Urals from 1943 to 2015 and from studies published since 1915. The dataset consists of 4,120 occurrence records. The occurrence data were extracted from herbarium specimen labels (3,833 records) and data from published literature (287 records). Most of the records (4,104) are georeferenced. A total of 302 moss taxa belonging to 112 genera and 36 families are reported herein to occur in Yugyd Va National Park. The diversity of bryophytes in this National Park has not yet been fully explored and further exploration will lead to more taxa. -
National Wetlands Inventory Map Report for Quinault Indian Nation
National Wetlands Inventory Map Report for Quinault Indian Nation Project ID(s): R01Y19P01: Quinault Indian Nation, fiscal year 2019 Project area The project area (Figure 1) is restricted to the Quinault Indian Nation, bounded by Grays Harbor Co. Jefferson Co. and the Olympic National Park. Appendix A: USGS 7.5-minute Quadrangles: Queets, Salmon River West, Salmon River East, Matheny Ridge, Tunnel Island, O’Took Prairie, Thimble Mountain, Lake Quinault West, Lake Quinault East, Taholah, Shale Slough, Macafee Hill, Stevens Creek, Moclips, Carlisle. • < 0. Figure 1. QIN NWI+ 2019 project area (red outline). Source Imagery: Citation: For all quads listed above: See Appendix A Citation Information: Originator: USDA-FSA-APFO Aerial Photography Field Office Publication Date: 2017 Publication place: Salt Lake City, Utah Title: Digital Orthoimagery Series of Washington Geospatial_Data_Presentation_Form: raster digital data Other_Citation_Details: 1-meter and 1-foot, Natural Color and NIR-False Color Collateral Data: . USGS 1:24,000 topographic quadrangles . USGS – NHD – National Hydrography Dataset . USGS Topographic maps, 2013 . QIN LiDAR DEM (3 meter) and synthetic stream layer, 2015 . Previous National Wetlands Inventories for the project area . Soil Surveys, All Hydric Soils: Weyerhaeuser soil survey 1976, NRCS soil survey 2013 . QIN WET tables, field photos, and site descriptions, 2016 to 2019, Janice Martin, and Greg Eide Inventory Method: Wetland identification and interpretation was done “heads-up” using ArcMap versions 10.6.1. US Fish & Wildlife Service (USFWS) National Wetlands Inventory (NWI) mapping contractors in Portland, Oregon completed the original aerial photo interpretation and wetland mapping. Primary authors: Nicholas Jones of SWCA Environmental Consulting. 100% Quality Control (QC) during the NWI mapping was provided by Michael Holscher of SWCA Environmental Consulting. -
National List of Vascular Plant Species That Occur in Wetlands 1996
National List of Vascular Plant Species that Occur in Wetlands: 1996 National Summary Indicator by Region and Subregion Scientific Name/ North North Central South Inter- National Subregion Northeast Southeast Central Plains Plains Plains Southwest mountain Northwest California Alaska Caribbean Hawaii Indicator Range Abies amabilis (Dougl. ex Loud.) Dougl. ex Forbes FACU FACU UPL UPL,FACU Abies balsamea (L.) P. Mill. FAC FACW FAC,FACW Abies concolor (Gord. & Glend.) Lindl. ex Hildebr. NI NI NI NI NI UPL UPL Abies fraseri (Pursh) Poir. FACU FACU FACU Abies grandis (Dougl. ex D. Don) Lindl. FACU-* NI FACU-* Abies lasiocarpa (Hook.) Nutt. NI NI FACU+ FACU- FACU FAC UPL UPL,FAC Abies magnifica A. Murr. NI UPL NI FACU UPL,FACU Abildgaardia ovata (Burm. f.) Kral FACW+ FAC+ FAC+,FACW+ Abutilon theophrasti Medik. UPL FACU- FACU- UPL UPL UPL UPL UPL NI NI UPL,FACU- Acacia choriophylla Benth. FAC* FAC* Acacia farnesiana (L.) Willd. FACU NI NI* NI NI FACU Acacia greggii Gray UPL UPL FACU FACU UPL,FACU Acacia macracantha Humb. & Bonpl. ex Willd. NI FAC FAC Acacia minuta ssp. minuta (M.E. Jones) Beauchamp FACU FACU Acaena exigua Gray OBL OBL Acalypha bisetosa Bertol. ex Spreng. FACW FACW Acalypha virginica L. FACU- FACU- FAC- FACU- FACU- FACU* FACU-,FAC- Acalypha virginica var. rhomboidea (Raf.) Cooperrider FACU- FAC- FACU FACU- FACU- FACU* FACU-,FAC- Acanthocereus tetragonus (L.) Humm. FAC* NI NI FAC* Acanthomintha ilicifolia (Gray) Gray FAC* FAC* Acanthus ebracteatus Vahl OBL OBL Acer circinatum Pursh FAC- FAC NI FAC-,FAC Acer glabrum Torr. FAC FAC FAC FACU FACU* FAC FACU FACU*,FAC Acer grandidentatum Nutt. -
Correction To: Testing the Moss Layer Transfer Technique on Mineral Well Pads Constructed in Peatlands
Wetlands Ecol Manage (2018) 26:489–490 https://doi.org/10.1007/s11273-018-9608-9 CORRECTION Correction to: Testing the moss layer transfer technique on mineral well pads constructed in peatlands Marie-Eve Gauthier . Line Rochefort . Leonie Nadeau . Sandrine Hugron . Bin Xu Published online: 28 May 2018 Ó Springer Science+Business Media B.V., part of Springer Nature 2018 Correction to: Wetlands Ecol Manage https://doi.org/10.1007/s11273-017-9532-4 In the original publication, the Table 1 was published incorrectly. The correct version of Table 1 is given in this correction. The original article has been corrected. The original article can be found online at https:// doi.org/10.1007/s11273-017-9532-4. M.-E. Gauthier Á L. Rochefort (&) Á S. Hugron Department of Plant Sciences and Centre for Northern Studies, Universite´ Laval, Que´bec, QC G1V 0A6, Canada e-mail: [email protected] L. Nadeau Á B. Xu NAIT Boreal Research Institute, Peace River, AB T8S 1R2, Canada 123 490 Wetlands Ecol Manage (2018) 26:489–490 Table 1 Description of fen plant communities used as source of propagules (donor sites) for the moss layer transfer experiment Treed Rich Fen Cover Shrubby Rich Fen Cover Plant composition Trees Picea mariana 10 – Shrubs Vaccinium vitis-idaea 12 Salix spp. 15 Larix laricina 9 Betula glandulosa 2 Chamaedaphne calyculata 8 Empetrum nigrum 4 Rhododendron groenlandicum 4 Salix spp. 4 Herbs Carex aquatilis 3 Carex aquatilis 7 Carex tenuiflora * Comarum palustre 2 Carex magellanica ssp. irrigua 1 Mosses Sphagum fuscum 55 Sphagnum angustifolium 30 Aulacomnium palustre 3 Tomentypnum nitens 15 Aulacomnium palustre 3 Water chem. -
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..................................................................................................... -
Action C.5 Milestone: Bryophyte Ex Situ Conservation Scheme Feb 2017
ESCAPE – UNIVERSITY OF HELSINKI Action C.5 Milestone Bryophyte ex situ conservation scheme Sanna Laaka-Lindberg & Xiaolan He 2/28/2017 Monitoring Meesia longiseta reintroduction site in 2016. Photo: Sanna Laaka-Lindberg An ex situ conservation scheme is presented on the basis of compiled results of the ESCAPE project as a model for bryophyte conservation. ESCAPE LIFE+2011 BIO/FI/917 Action C.5 Milestone Bryophyte ex situ conservation scheme Introduction Ex situ conservation is a species conservation method used as a compliment to the primary conservation tool in situ conservation, a process of protecting an endangered species in its natural habitat. Ex situ conservation is targeted to species in most serious threat, especially when the conservation measures in nature are not adequate for species survival. There are basically two different types of ex situ conservation tools: 1) tools aimed at storing and securing the species and its genetic variation e.g. on national or even on wider (global) level, and 2) tools aimed at increasing species survival ability in nature. The ultimate goal of ex situ conservation is to provide support for the survival of species in their natural environments. Conservation of biodiversity is a continuous and long-term assignment, so the decisions on ex situ conservation to a species need to be made on a solid basis. This involves thorough investigation on conservation priorities, background knowledge of the biology and ecology of the species to be conserved, and the feasibility of the conservation plan. In the ESCAPE project, a priority list was compiled for vascular plants (see Ryttäri 2013), but no such list is made for bryophytes. -
CBD First National Report
FIRST NATIONAL REPORT OF THE REPUBLIC OF SERBIA TO THE UNITED NATIONS CONVENTION ON BIOLOGICAL DIVERSITY July 2010 ACRONYMS AND ABBREVIATIONS .................................................................................... 3 1. EXECUTIVE SUMMARY ........................................................................................... 4 2. INTRODUCTION ....................................................................................................... 5 2.1 Geographic Profile .......................................................................................... 5 2.2 Climate Profile ...................................................................................................... 5 2.3 Population Profile ................................................................................................. 7 2.4 Economic Profile .................................................................................................. 7 3 THE BIODIVERSITY OF SERBIA .............................................................................. 8 3.1 Overview......................................................................................................... 8 3.2 Ecosystem and Habitat Diversity .................................................................... 8 3.3 Species Diversity ............................................................................................ 9 3.4 Genetic Diversity ............................................................................................. 9 3.5 Protected Areas .............................................................................................10