Moehringia Macrophylla (Hook.) Fenzl Large-Leaved Sandwort
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												Appendix 1. Results for the Species Not in Database
Supporting information for: Pärtel, J., Pärtel, M. & Wäldchen, J. 2021. Plant image identification application demonstrates high accuracy in Northern Europe. AoB PLANTS. Appendix 1. Results for the species not in database Taxa not known to the machine learning model, i.e. those on which the classifier was not trained, could not be recognized. The model is unable to determine whether an image belongs to an unknown taxon it has never seen before and will wrongly identify a known taxon with the highest degree of similarity. Typically, the highest degree of similarity is still so low that no suggestions will be given for the user. Here we extracted the best match information directly from the Flora Incognita server but did not use these species in our analyses since the model’s prediction can only be interpreted in a meaningful way for taxa on which it was actually trained. The five unknown species were only found in the database study. Some of them were garden plants, or had a northern or eastern distribution. (1) Draba incana has an arcotmontane distribution which reach its SW border in Estonia, the most similar species in the Flora Incognita database was Arabis hirsuta. (2) Lychnis chalcedonica originates from continental Eurasia but is used as an ornamental garden plant. In Estonia it sometimes spreads to nature. Flora Incognita is focusing on European natural plants, even if many naturalized ones are included. The most similar species found was Phlox paniculata. (3) Moehringia lateriflora is distributed in Eurasia, reaching in its E border in Estonia. The most similar match was Cardamine californica. - 
												
												Outline of Angiosperm Phylogeny
Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese - 
												
												Untangling Phylogenetic Patterns and Taxonomic Confusion in Tribe Caryophylleae (Caryophyllaceae) with Special Focus on Generic
TAXON 67 (1) • February 2018: 83–112 Madhani & al. • Phylogeny and taxonomy of Caryophylleae (Caryophyllaceae) Untangling phylogenetic patterns and taxonomic confusion in tribe Caryophylleae (Caryophyllaceae) with special focus on generic boundaries Hossein Madhani,1 Richard Rabeler,2 Atefeh Pirani,3 Bengt Oxelman,4 Guenther Heubl5 & Shahin Zarre1 1 Department of Plant Science, Center of Excellence in Phylogeny of Living Organisms, School of Biology, College of Science, University of Tehran, P.O. Box 14155-6455, Tehran, Iran 2 University of Michigan Herbarium-EEB, 3600 Varsity Drive, Ann Arbor, Michigan 48108-2228, U.S.A. 3 Department of Biology, Faculty of Sciences, Ferdowsi University of Mashhad, P.O. Box 91775-1436, Mashhad, Iran 4 Department of Biological and Environmental Sciences, University of Gothenburg, Box 461, 40530 Göteborg, Sweden 5 Biodiversity Research – Systematic Botany, Department of Biology I, Ludwig-Maximilians-Universität München, Menzinger Str. 67, 80638 München, Germany; and GeoBio Center LMU Author for correspondence: Shahin Zarre, [email protected] DOI https://doi.org/10.12705/671.6 Abstract Assigning correct names to taxa is a challenging goal in the taxonomy of many groups within the Caryophyllaceae. This challenge is most serious in tribe Caryophylleae since the supposed genera seem to be highly artificial, and the available morphological evidence cannot effectively be used for delimitation and exact determination of taxa. The main goal of the present study was to re-assess the monophyly of the genera currently recognized in this tribe using molecular phylogenetic data. We used the sequences of nuclear ribosomal internal transcribed spacer (ITS) and the chloroplast gene rps16 for 135 and 94 accessions, respectively, representing all 16 genera currently recognized in the tribe Caryophylleae, with a rich sampling of Gypsophila as one of the most heterogeneous groups in the tribe. - 
												
												Desmodium Cuspidatum (Muhl.) Loudon Large-Bracted Tick-Trefoil
New England Plant Conservation Program Desmodium cuspidatum (Muhl.) Loudon Large-bracted Tick-trefoil Conservation and Research Plan for New England Prepared by: Lynn C. Harper Habitat Protection Specialist Massachusetts Natural Heritage and Endangered Species Program Westborough, Massachusetts For: New England Wild Flower Society 180 Hemenway Road Framingham, MA 01701 508/877-7630 e-mail: [email protected] • website: www.newfs.org Approved, Regional Advisory Council, 2002 SUMMARY Desmodium cuspidatum (Muhl.) Loudon (Fabaceae) is a tall, herbaceous, perennial legume that is regionally rare in New England. Found most often in dry, open, rocky woods over circumneutral to calcareous bedrock, it has been documented from 28 historic and eight current sites in the three states (Vermont, New Hampshire, and Massachusetts) where it is tracked by the Natural Heritage programs. The taxon has not been documented from Maine. In Connecticut and Rhode Island, the species is reported but not tracked by the Heritage programs. Two current sites in Connecticut are known from herbarium specimens. No current sites are known from Rhode Island. Although secure throughout most of its range in eastern and midwestern North America, D. cuspidatum is Endangered in Vermont, considered Historic in New Hampshire, and watch-listed in Massachusetts. It is ranked G5 globally. Very little is understood about the basic biology of this species. From work on congeners, it can be inferred that there are likely to be no problems with pollination, seed set, or germination. As for most legumes, rhizobial bacteria form nitrogen-fixing nodules on the roots of D. cuspidatum. It is unclear whether there have been any changes in the numbers or distribution of rhizobia capable of forming effective mutualisms with D. - 
												
												Moehringia Lateriflora
Report under the Article 17 of the Habitats Directive European Environment Period 2007-2012 Agency European Topic Centre on Biological Diversity Moehringia lateriflora Annex II, IV Priority No Species group Vascular plants Regions Boreal Moehringia lateriflora is a flowering plant with circumpolar distribution including Russia, China, Japan and North America. Within the European Union it occur only in the Boreal region and is very rare in Estonia and Sweden, more widespread in Finland. It grows mainly on stony shores, grazed dry or moist wooded meadows and forest edges. The species Considered "Favourable" in Estonia and Sweden, but not in Finland. Majority of the population in Sweden, but in a few sites. Overall assessment is "Unfavourable Inadequate", due to the situation in Finland. Trend stable. Main threats are changes in hydraulic conditions and lack of grazing. No changes in overall conservation status between 2001-06 and 2007-12 reports. Page 1 Species: Moehringia lateriflora Report under the Article 17 of the Habitats Directive Assessment of conservation status at the European biogeographical level Conservation status (CS) of parameters Current Trend in % in Previous Reason for Region Future CS CS region CS change Range Population Habitat prospects BOR FV FV U1 U1 U1 = 100 U1 See the endnote for more informationi Assessment of conservation status at the Member State level Page 2 Species: Moehringia lateriflora Report under the Article 17 of the Habitats Directive Assessment of conservation status at the Member State level The map shows both Conservation Status and distribution using a 10 km x 10 km grid. Conservation status is assessed at biogeographical level. - 
												
												Taxonomic Studi Es on Thearenaria Serpyllifolia Group (Caryophyllaceae)
Flora Mediterranea lO - 2000 185 Mohamed N. Abuhadra Taxonomic studies on theArenaria serpyllifolia group (Caryophyllaceae) Abstract Abuhadra, M. N.: Taxonomic studies on the Arenaria serpy//ifolia group (Caryophyllaceae). Fl. Medit. lO : 185-190.2000. - ISSN 1120-4052. Scanning electron microscopic investigation of seed and capsule morphology of Arenaria ser pyllifolia L. and A. leptoclados Guss. In the Caryophy/laceae have been studied. Seed size in both species show consistency, but testa ornamentation (midzone) vary in shape even in the seeds from one capsule of A. serpyfolia, while in A. leptoclados midzone cells are narrowly elongate in different populations and environments. The ripe capsule teeth ornamentation has a diagnosti c character lO separate A. serpy/lifolia and A. leptoclados. lntroduction The group Arenaria serpyllifolia (Caryophyllaceae), includes some taxa, thet in tum has often been considered at specific or subspecific rank. McNeii (1963) regarded seed size as the most satisfactory character separating the tetraploid A. serpyllifolia L. from the diploid A. leptoclados, both automatically self-pollinating species. Perring and Sell (1967) used seed characters but not those of the testa to separate the subspecies lepto clados, serpyllifolia and macrocarpa (Lloyd) Perring & Sell. In the first edition of Flora Europaea A. serpyllifolia and A. leptoclados are treated as species (Charter & Halliday 1964) but in the second they are regarded as subspecies (Charter & Halliday 1993). Greuter & al. (1984) recognised as species the following in the Mediterranean area: A. argaea Rech. f, A. leptoclados (Rchnb.) Guss., A. marschlinsii Koch, A. minutiflora Loscos [doubtful status], A. peloponnesiaca Rech. fil. and A serpyllifolia L .. For Britain Stace (1991), accepts subspecific status: serpyllifolia, leptoclados (Reichenb.) Nyman and Lloydii (Jordan) Bonnier (A . - 
												
												Kenai National Wildlife Refuge Species List, Version 2018-07-24
Kenai National Wildlife Refuge Species List, version 2018-07-24 Kenai National Wildlife Refuge biology staff July 24, 2018 2 Cover image: map of 16,213 georeferenced occurrence records included in the checklist. Contents Contents 3 Introduction 5 Purpose............................................................ 5 About the list......................................................... 5 Acknowledgments....................................................... 5 Native species 7 Vertebrates .......................................................... 7 Invertebrates ......................................................... 55 Vascular Plants........................................................ 91 Bryophytes ..........................................................164 Other Plants .........................................................171 Chromista...........................................................171 Fungi .............................................................173 Protozoans ..........................................................186 Non-native species 187 Vertebrates ..........................................................187 Invertebrates .........................................................187 Vascular Plants........................................................190 Extirpated species 207 Vertebrates ..........................................................207 Vascular Plants........................................................207 Change log 211 References 213 Index 215 3 Introduction Purpose to avoid implying - 
												
												Emerald Network Rapport Engelsk.Indd
DN Report 2007 - 1b Emerald Network in Norway – Final Report from the Pilot Project 1 Emerald Network in Norway - Final Report from the Pilot Project Report 2007 – 1b ABSTRACT: Publisher: Emerald Network is a network of important sites for conservation Directorate for Nature of biodiversity in Europe under the Berne Convention. Norway is Management obligated to participate and to contribute to this network. The fi rst step is to carry out a pilot project where each country reports its specifi c obligations. Emerald Network can be seen as a parallel Date published: september 2007 network to Natura 2000 under the Habitat and Birds Directives in (English version) the European Union. Emerald Network builds upon the same conditions with focus on species and natural habitats. Antall sider: 58 In this report, the Directorate for Nature Management presents results and recommendations from the Norwegian Pilot Project. Keywords: The results show that Norway will contribute considerably with Ecological Networks, Bio- important sites for European biodiversity into this network. diversity, European Cooperation, Protected areas in Norway hold important qualities which are Bern Convention, Protected demanded in the Berne Convention, and a majority of the protected Areas areas satisfi es the criteria in Emerald Network. The Pilot Project forms the basis for the second phase, which is the Contact adress: implementation of the Network itself. In this phase, all the sites that Directorate for Nature meet the criteria should be nominated. Important areas for species Management and/or natural habitats that are not included in existing protected 7485 Trondheim areas should be considered. In Norway this will be coordinated Norway with the ongoing evaluation of our existing protected areas net- Phone: +47 73 58 05 00 work. - 
												
												Species Using RAPD Markers
İ. ERÖZ POYRAZ, E. SÖZEN, E. ATAŞLAR, İ. POYRAZ Turk J Biol 36 (2012) 293-302 © TÜBİTAK doi:10.3906/biy-1012-177 Determination of genetic relationships among Velezia L. (Caryophyllaceae) species using RAPD markers İlham ERÖZ POYRAZ1, Emel SÖZEN2, Ebru ATAŞLAR3, İsmail POYRAZ4 1Department of Pharmaceutical Botany, Faculty of Pharmacy, Anadolu University, 26470 Eskişehir - TURKEY 2Department of Biology, Faculty of Sciences, Anadolu University, 26470 Eskişehir - TURKEY 3Department of Biology, Faculty of Science and Literature, Eskişehir Osmangazi University, 26480 Eskişehir - TURKEY 4Department of Molecular Biology and Genetics, Faculty of Science and Letters, Bilecik University, 11210 Gülümbe, Bilecik - TURKEY Received: 24.12.2010 Abstract: Random amplifi ed polymorphic DNA (RAPD) markers were used to determine genetic relationships among Velezia L. species from Turkey. A total of 432 amplifi ed bands were obtained using 14 RAPD primers. Th e polymorphism in RAPD markers was high (98.61%) and was suffi cient to distinguish each species. Th e degree of band-sharing was used for evaluating the genetic similarity between species and for constructing a dendrogram by the unweighted pair group method with arithmetic mean (UPGMA). Genetic relationships among the species were found to be fully consistent with those obtained by the use of morphological characters. Data obtained from our study demonstrated that the RAPD technique could be successfully used for the determination of genetic relationships among Velezia species and for species identifi cation. Furthermore, it can be effi ciently employed in future studies to provide preliminary data for conservation of endangered Velezia species. Key words: Genetic relationships, RAPD-PCR, Velezia L., Turkey RAPD markörleri kullanılarak Velezia L. - 
												
												Sensitive Species That Are Not Listed Or Proposed Under the ESA Sorted By: Major Group, Subgroup, NS Sci
Forest Service Sensitive Species that are not listed or proposed under the ESA Sorted by: Major Group, Subgroup, NS Sci. Name; Legend: Page 94 REGION 10 REGION 1 REGION 2 REGION 3 REGION 4 REGION 5 REGION 6 REGION 8 REGION 9 ALTERNATE NATURESERVE PRIMARY MAJOR SUB- U.S. N U.S. 2005 NATURESERVE SCIENTIFIC NAME SCIENTIFIC NAME(S) COMMON NAME GROUP GROUP G RANK RANK ESA C 9 Anahita punctulata Southeastern Wandering Spider Invertebrate Arachnid G4 NNR 9 Apochthonius indianensis A Pseudoscorpion Invertebrate Arachnid G1G2 N1N2 9 Apochthonius paucispinosus Dry Fork Valley Cave Invertebrate Arachnid G1 N1 Pseudoscorpion 9 Erebomaster flavescens A Cave Obligate Harvestman Invertebrate Arachnid G3G4 N3N4 9 Hesperochernes mirabilis Cave Psuedoscorpion Invertebrate Arachnid G5 N5 8 Hypochilus coylei A Cave Spider Invertebrate Arachnid G3? NNR 8 Hypochilus sheari A Lampshade Spider Invertebrate Arachnid G2G3 NNR 9 Kleptochthonius griseomanus An Indiana Cave Pseudoscorpion Invertebrate Arachnid G1 N1 8 Kleptochthonius orpheus Orpheus Cave Pseudoscorpion Invertebrate Arachnid G1 N1 9 Kleptochthonius packardi A Cave Obligate Pseudoscorpion Invertebrate Arachnid G2G3 N2N3 9 Nesticus carteri A Cave Spider Invertebrate Arachnid GNR NNR 8 Nesticus cooperi Lost Nantahala Cave Spider Invertebrate Arachnid G1 N1 8 Nesticus crosbyi A Cave Spider Invertebrate Arachnid G1? NNR 8 Nesticus mimus A Cave Spider Invertebrate Arachnid G2 NNR 8 Nesticus sheari A Cave Spider Invertebrate Arachnid G2? NNR 8 Nesticus silvanus A Cave Spider Invertebrate Arachnid G2? NNR - 
												
												Interpretation Manual of European Union Habitats-Aprile 2013
INTERPRETATION MANUAL OF EUROPEAN UNION HABITATS EUR 28 April 2013 EUROPEAN COMMISSION DG ENVIRONMENT Nature ENV B.3 The Interpretation Manual of European Union Habitats - EUR28 is a scientific reference document. It is based on the version for EUR15, which was adopted by the Habitats Committee on 4. October 1999 and consolidated with the new and amended habitat types for the 10 accession countries as adopted by the Habitats Committee on 14 March 2002. A small amendment to habitat type 91D0 was adopted by the Habitats Committee in its meeting on 14th October 2003. The Habitats Committee at its meeting on 13 April 2007 adopted additional changes for the accession of Bulgaria and Romania, and for the marine habitats, followed the descriptions given in “Guidelines for the establishment of the Natura 2000 network in the marine environment. Application of the Habitats and Birds Directives” published in May 2007 by the Commission services. Amendments for the accession of Croatia were adopted by the Habitats Committee on 4 October, 2012. The April 2013 version consolidates the changes for Croatia in the text and corrects the references to EUNIS codes for three marine habitat types. TABLE OF CONTENTS WHY THIS MANUAL? 3 HISTORICAL REVIEW 3 THE MANUAL 4 THE EUR15 VERSION 5 THE EUR25 VERSION 5 THE EUR27 VERSION 6 THE EUR28 VERSION 6 EXPLANATORY NOTES 7 COASTAL AND HALOPHYTIC HABITATS 7 COASTAL AND HALOPHYTIC HABITATS 8 OPEN SEA AND TIDAL AREAS 8 SEA CLIFFS AND SHINGLE OR STONY BEACHES 17 ATLANTIC AND CONTINENTAL SALT MARSHES AND SALT MEADOWS 20 - 
												
												Flora-Lab-Manual.Pdf
LabLab MManualanual ttoo tthehe Jane Mygatt Juliana Medeiros Flora of New Mexico Lab Manual to the Flora of New Mexico Jane Mygatt Juliana Medeiros University of New Mexico Herbarium Museum of Southwestern Biology MSC03 2020 1 University of New Mexico Albuquerque, NM, USA 87131-0001 October 2009 Contents page Introduction VI Acknowledgments VI Seed Plant Phylogeny 1 Timeline for the Evolution of Seed Plants 2 Non-fl owering Seed Plants 3 Order Gnetales Ephedraceae 4 Order (ungrouped) The Conifers Cupressaceae 5 Pinaceae 8 Field Trips 13 Sandia Crest 14 Las Huertas Canyon 20 Sevilleta 24 West Mesa 30 Rio Grande Bosque 34 Flowering Seed Plants- The Monocots 40 Order Alistmatales Lemnaceae 41 Order Asparagales Iridaceae 42 Orchidaceae 43 Order Commelinales Commelinaceae 45 Order Liliales Liliaceae 46 Order Poales Cyperaceae 47 Juncaceae 49 Poaceae 50 Typhaceae 53 Flowering Seed Plants- The Eudicots 54 Order (ungrouped) Nymphaeaceae 55 Order Proteales Platanaceae 56 Order Ranunculales Berberidaceae 57 Papaveraceae 58 Ranunculaceae 59 III page Core Eudicots 61 Saxifragales Crassulaceae 62 Saxifragaceae 63 Rosids Order Zygophyllales Zygophyllaceae 64 Rosid I Order Cucurbitales Cucurbitaceae 65 Order Fabales Fabaceae 66 Order Fagales Betulaceae 69 Fagaceae 70 Juglandaceae 71 Order Malpighiales Euphorbiaceae 72 Linaceae 73 Salicaceae 74 Violaceae 75 Order Rosales Elaeagnaceae 76 Rosaceae 77 Ulmaceae 81 Rosid II Order Brassicales Brassicaceae 82 Capparaceae 84 Order Geraniales Geraniaceae 85 Order Malvales Malvaceae 86 Order Myrtales Onagraceae