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Pharmacognostical Identification of Alchemilla Japonica Nakai Et Hara
© 2015 Journal of Pharmacy & Pharmacognosy Research, 3 (3), 59-68 ISSN 0719-4250 http://jppres.com/jppres Original Article | Artículo Original Pharmacognostical identification of Alchemilla japonica Nakai et Hara [Identificación farmacognóstica de Alchemilla japonica Nakai et Hara] Yun Zhu, Ningjing Zhang, Peng Li* School of Pharmacy, Shihezi University/Key Laboratory of Phytomedicine Resources & Modernization of TCM, Shihezi Xinjiang 832002, PR China. * E-mail: [email protected] Abstract Resumen Context: Alchemilla japonica is a therapeutically important medicinal Contexto: Alchemilla japonica es una planta medicinal, terapéutica- plant, which is widely used in traditional medicine external application mente importante, que se utiliza ampliamente en la medicina tradicional for injuries as well as orally for acute diarrhea, dysmenorrhea, and por aplicación externa en lesiones, así como por vía oral para la diarrea menorrhagia, among others. However, there is not a correct identification aguda, dismenorrea y menorragia, entre otras. Sin embargo, no hay una of this species and is of prime importance differentiate it from commonly correcta identificación de la especie y es de primordial importancia available adulterants or substitutes, in fresh, dried or powdered state. diferenciar esta de adulterantes comúnmente disponibles o sustitutos, en There is only a small number of data of pharmacological standards for estado fresco, seco o en polvo. Sólo hay un pequeño número de datos de identification and authentication of A. japonica. patrones farmacológicos para la identificación y autenticación de A. Aims: To characterize morpho-anatomically the roots, leaves and stems japonica. of Alchemilla japonica Nakai et Hara (Rosaceae), explore and establish the Objetivos: Caracterizar desde el punto de vista morfo-anatómico las micromorphology and quality control method for this plant. -
Analysis of Paralogs in Target Enrichment Data Pinpoints Multiple Ancient Polyploidy Events
bioRxiv preprint doi: https://doi.org/10.1101/2020.08.21.261925; this version posted August 23, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 1 Analysis of paralogs in target enrichment data pinpoints multiple ancient polyploidy events 2 in Alchemilla s.l. (Rosaceae). 3 4 Diego F. Morales-Briones1.2,*, Berit Gehrke3, Chien-Hsun Huang4, Aaron Liston5, Hong Ma6, 5 Hannah E. Marx7, David C. Tank2, Ya Yang1 6 7 1Department of Plant and Microbial Biology, University of Minnesota-Twin Cities, 1445 Gortner 8 Avenue, St. Paul, MN 55108, USA 9 2Department of Biological Sciences and Institute for Bioinformatics and Evolutionary Studies, 10 University of Idaho, 875 Perimeter Drive MS 3051, Moscow, ID 83844, USA 11 3University Gardens, University Museum, University of Bergen, Mildeveien 240, 5259 12 Hjellestad, Norway 13 4State Key Laboratory of Genetic Engineering and Collaborative Innovation Center of Genetics 14 and Development, Ministry of Education Key Laboratory of Biodiversity and Ecological 15 Engineering, Institute of Plant Biology, Center of Evolutionary Biology, School of Life Sciences, 16 Fudan University, Shanghai 200433, China 17 5Department of Botany and Plant Pathology, Oregon State University, 2082 Cordley Hall, 18 Corvallis, OR 97331, USA 19 6Department of Biology, the Huck Institute of the Life Sciences, the Pennsylvania State 20 University, 510D Mueller Laboratory, University Park, PA 16802 USA 21 7Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, MI 22 48109-1048, USA 23 bioRxiv preprint doi: https://doi.org/10.1101/2020.08.21.261925; this version posted August 23, 2020. -
ED45E Rare and Scarce Species Hierarchy.Pdf
104 Species 55 Mollusc 8 Mollusc 334 Species 181 Mollusc 28 Mollusc 44 Species 23 Vascular Plant 14 Flowering Plant 45 Species 23 Vascular Plant 14 Flowering Plant 269 Species 149 Vascular Plant 84 Flowering Plant 13 Species 7 Mollusc 1 Mollusc 42 Species 21 Mollusc 2 Mollusc 43 Species 22 Mollusc 3 Mollusc 59 Species 30 Mollusc 4 Mollusc 59 Species 31 Mollusc 5 Mollusc 68 Species 36 Mollusc 6 Mollusc 81 Species 43 Mollusc 7 Mollusc 105 Species 56 Mollusc 9 Mollusc 117 Species 63 Mollusc 10 Mollusc 118 Species 64 Mollusc 11 Mollusc 119 Species 65 Mollusc 12 Mollusc 124 Species 68 Mollusc 13 Mollusc 125 Species 69 Mollusc 14 Mollusc 145 Species 81 Mollusc 15 Mollusc 150 Species 84 Mollusc 16 Mollusc 151 Species 85 Mollusc 17 Mollusc 152 Species 86 Mollusc 18 Mollusc 158 Species 90 Mollusc 19 Mollusc 184 Species 105 Mollusc 20 Mollusc 185 Species 106 Mollusc 21 Mollusc 186 Species 107 Mollusc 22 Mollusc 191 Species 110 Mollusc 23 Mollusc 245 Species 136 Mollusc 24 Mollusc 267 Species 148 Mollusc 25 Mollusc 270 Species 150 Mollusc 26 Mollusc 333 Species 180 Mollusc 27 Mollusc 347 Species 189 Mollusc 29 Mollusc 349 Species 191 Mollusc 30 Mollusc 365 Species 196 Mollusc 31 Mollusc 376 Species 203 Mollusc 32 Mollusc 377 Species 204 Mollusc 33 Mollusc 378 Species 205 Mollusc 34 Mollusc 379 Species 206 Mollusc 35 Mollusc 404 Species 221 Mollusc 36 Mollusc 414 Species 228 Mollusc 37 Mollusc 415 Species 229 Mollusc 38 Mollusc 416 Species 230 Mollusc 39 Mollusc 417 Species 231 Mollusc 40 Mollusc 418 Species 232 Mollusc 41 Mollusc 419 Species 233 -
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 -
Conserving Europe's Threatened Plants
Conserving Europe’s threatened plants Progress towards Target 8 of the Global Strategy for Plant Conservation Conserving Europe’s threatened plants Progress towards Target 8 of the Global Strategy for Plant Conservation By Suzanne Sharrock and Meirion Jones May 2009 Recommended citation: Sharrock, S. and Jones, M., 2009. Conserving Europe’s threatened plants: Progress towards Target 8 of the Global Strategy for Plant Conservation Botanic Gardens Conservation International, Richmond, UK ISBN 978-1-905164-30-1 Published by Botanic Gardens Conservation International Descanso House, 199 Kew Road, Richmond, Surrey, TW9 3BW, UK Design: John Morgan, [email protected] Acknowledgements The work of establishing a consolidated list of threatened Photo credits European plants was first initiated by Hugh Synge who developed the original database on which this report is based. All images are credited to BGCI with the exceptions of: We are most grateful to Hugh for providing this database to page 5, Nikos Krigas; page 8. Christophe Libert; page 10, BGCI and advising on further development of the list. The Pawel Kos; page 12 (upper), Nikos Krigas; page 14: James exacting task of inputting data from national Red Lists was Hitchmough; page 16 (lower), Jože Bavcon; page 17 (upper), carried out by Chris Cockel and without his dedicated work, the Nkos Krigas; page 20 (upper), Anca Sarbu; page 21, Nikos list would not have been completed. Thank you for your efforts Krigas; page 22 (upper) Simon Williams; page 22 (lower), RBG Chris. We are grateful to all the members of the European Kew; page 23 (upper), Jo Packet; page 23 (lower), Sandrine Botanic Gardens Consortium and other colleagues from Europe Godefroid; page 24 (upper) Jože Bavcon; page 24 (lower), Frank who provided essential advice, guidance and supplementary Scumacher; page 25 (upper) Michael Burkart; page 25, (lower) information on the species included in the database. -
Download (592Kb)
This is an Open Access document downloaded from ORCA, Cardiff University's institutional repository: http://orca.cf.ac.uk/134581/ This is the author’s version of a work that was submitted to / accepted for publication. Citation for final published version: Raye, Lee 2020. The wild plants of Scotia Illustrata (1684). British & Irish Botany 2 (3) , pp. 240- 258. 10.33928/bib.2020.02.240 file Publishers page: http://dx.doi.org/10.33928/bib.2020.02.240 <http://dx.doi.org/10.33928/bib.2020.02.240> Please note: Changes made as a result of publishing processes such as copy-editing, formatting and page numbers may not be reflected in this version. For the definitive version of this publication, please refer to the published source. You are advised to consult the publisher’s version if you wish to cite this paper. This version is being made available in accordance with publisher policies. See http://orca.cf.ac.uk/policies.html for usage policies. Copyright and moral rights for publications made available in ORCA are retained by the copyright holders. British & Irish Botany 2(3): 240-258, 2020 The wild plants of Scotia Illustrata (1684) Lee Raye Cardiff University, Wales, UK Corresponding author: Lee Raye: [email protected] This pdf constitutes the Version of Record published on 31st August 2020 Abstract Scotia Illustrata was published in 1684 and contains a section (II:1) describing 662 ‘naturally occurring plants of Scotland’. This paper sets out to identify and discuss the species in the text. It was possible to identify 652 species from the text and 396 could be securely identified. -
Palouse Forbs for Landscaping
More Palouse Forbs for Landscaping. by David M. Skinner, Paul Warnick, Bill French, and Mary Fauci November, 2005 The following is an additional list of native forbs which may be found in the Palouse region. These forbs may be less suitable for the landscape because of growth habit, aggressiveness, difficulty in propagating and growing, rarity, or it simply may be that we haven’t yet tried to do anything with them. For a list of Palouse forbs which may be more suitable for landscaping and about which we have more information to share, please see “Characteristics and Uses of Native Palouse Forbs in Landscaping.” Nomenclature used in this document also follows Hitchcock, C. Leo, and Arthur Cronquist. 1973. Flora of the Pacific Northwest. Univ. of Washington Press. Seattle, WA. In order to facilitate searching for a particular species, we have included some common names and alternate scientific names, but this is by no means intended to be a comprehensive source of common names or synonyms. Detailed information on propagation of many native species can be found at <http://nativeplants.for.uidaho.edu/network/search.asp?SearchType=Continental> Agastache urticifolia is probably too large a plant for a small garden. Requires a moist site. Easy to grow from seed. Plants have a minty smell and a very interesting flower. Common names include nettle-leafed giant hyssop, horsemint. Agoseris grandiflora is not a particularly attractive plant, it looks rather like a weed. Short-lived and attracts rodents, which eat the taproot and kill the plants. Easy to grow from seed, which is wind-borne and goes everywhere. -
Lundberg Et Al. 2009
Molecular Phylogenetics and Evolution 51 (2009) 269–280 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Allopolyploidy in Fragariinae (Rosaceae): Comparing four DNA sequence regions, with comments on classification Magnus Lundberg a,*, Mats Töpel b, Bente Eriksen b, Johan A.A. Nylander a, Torsten Eriksson a,c a Department of Botany, Stockholm University, SE-10691, Stockholm, Sweden b Department of Environmental Sciences, Gothenburg University, Box 461, SE-40530, Göteborg, Sweden c Bergius Foundation, Royal Swedish Academy of Sciences, SE-10405, Stockholm, Sweden article info abstract Article history: Potential events of allopolyploidy may be indicated by incongruences between separate phylogenies Received 23 June 2008 based on plastid and nuclear gene sequences. We sequenced two plastid regions and two nuclear ribo- Revised 25 February 2009 somal regions for 34 ingroup taxa in Fragariinae (Rosaceae), and six outgroup taxa. We found five well Accepted 26 February 2009 supported incongruences that might indicate allopolyploidy events. The incongruences involved Aphanes Available online 5 March 2009 arvensis, Potentilla miyabei, Potentilla cuneata, Fragaria vesca/moschata, and the Drymocallis clade. We eval- uated the strength of conflict and conclude that allopolyploidy may be hypothesised in the four first Keywords: cases. Phylogenies were estimated using Bayesian inference and analyses were evaluated using conver- Allopolyploidy gence diagnostics. Taxonomic implications are discussed for genera such as Alchemilla, Sibbaldianthe, Cha- Fragariinae Incongruence maerhodos, Drymocallis and Fragaria, and for the monospecific Sibbaldiopsis and Potaninia that are nested Molecular phylogeny inside other genera. Two orphan Potentilla species, P. miyabei and P. cuneata are placed in Fragariinae. -
Second Contribution to the Vascular Flora of the Sevastopol Area
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Wulfenia Jahr/Year: 2015 Band/Volume: 22 Autor(en)/Author(s): Seregin Alexey P., Yevseyenkow Pavel E., Svirin Sergey A., Fateryga Alexander Artikel/Article: Second contribution to the vascular flora of the Sevastopol area (the Crimea) 33-82 © Landesmuseum für Kärnten; download www.landesmuseum.ktn.gv.at/wulfenia; www.zobodat.at Wulfenia 22 (2015): 33 – 82 Mitteilungen des Kärntner Botanikzentrums Klagenfurt Second contribution to the vascular flora of the Sevastopol area (the Crimea) Alexey P. Seregin, Pavel E. Yevseyenkov, Sergey A. Svirin & Alexander V. Fateryga Summary: We report 323 new vascular plant species for the Sevastopol area, an administrative unit in the south-western Crimea. Records of 204 species are confirmed by herbarium specimens, 60 species have been reported recently in literature and 59 species have been either photographed or recorded in field in 2008 –2014. Seventeen species and nothospecies are new records for the Crimea: Bupleurum veronense, Lemna turionifera, Typha austro-orientalis, Tyrimnus leucographus, × Agrotrigia hajastanica, Arctium × ambiguum, A. × mixtum, Potamogeton × angustifolius, P. × salicifolius (natives and archaeophytes); Bupleurum baldense, Campsis radicans, Clematis orientalis, Corispermum hyssopifolium, Halimodendron halodendron, Sagina apetala, Solidago gigantea, Ulmus pumila (aliens). Recently discovered Calystegia soldanella which was considered to be extinct in the Crimea is the most important confirmation of historical records. The Sevastopol area is one of the most floristically diverse areas of Eastern Europe with 1859 currently known species. Keywords: Crimea, checklist, local flora, taxonomy, new records A checklist of vascular plants recorded in the Sevastopol area was published seven years ago (Seregin 2008). -
Figure S1. Maximum Likelihood Phylogeny of Alchemilla S.L
a) RT - ASTRAL 91/0.7 Alchemilla decumbens Eualchemilla - lobed 66/— Alchemilla heptagona 91/0.97 Alchemilla glabra 90/— Alchemilla japonica 1 Eualchemilla - dissected Alchemilla indivisa coalescent unit 90/— * 0.10 Alchemilla mollis Aphanes ‘lobed’ clade −0.21/0.29/0.99 100/0.84 * Alchemilla flabellata Alchemilla xanthochlora 100/0.94 Eualchemilla Lachemilla * Alchemilla plicata 0.62/0.17/0.99 Alchemilla lapeyrousii Alchemilla fissa Afromilla 99/0.63 75/— Alchemilla splendens Farinopsis salesoviana 0.023/0.87/0.98 * Alchemilla subsericea Alchemilla alpina ‘dissected’ clade * Alchemilla pentaphyllea 0.98/0/1 * 43/— Aphanes sp. “patagonica” Aphanes sp. “boliviana” 1/—/1 47/— * Aphanes cotopaxiensis * Aphanes occidentalis Aphanes * Aphanes microcarpa * Aphanes australis 1/—/1 Aphanes arvensis * Alchemilla fischeri 99/— Alchemilla cryptantha 11/1 100/— Alchemilla kiwuensis Alchemilla ellenbeckii 0.18/0.66/0.99 99/0.61 * Alchemilla schizophylla * Alchemilla hildebrandtii 73/— Alchemilla rutenbergii * Alchemilla colura * Alchemilla woodii * Alchemilla elongata Afromilla Alchemilla johnstonii 2/0.92 * Alchemilla microbetula Alchemilla haumanii 97/— Alchemilla stuhlmannii Alchemilla triphylla * 98/— * Alchemilla subnivalis 1/—/1 * Alchemilla argyrophylla Alchemilla roccatii 100/0.95 Lachemilla moritziana Alchemilla s.l. * Lachemilla aphanoides * Lachemilla standleyi 1/—/1 42/— * Lachemilla procumbens 93/1 Lachemilla hirta Lachemilla sibbaldiifolia * * Lachemilla jamesonii * Lachemilla vulcanica 95/1 Lachemilla andina 95/— Lachemilla pringlei -
Synopsis of a New Taxonomic Synthesis Of
Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 8 October 2018 doi:10.20944/preprints201808.0496.v2 Hershkovitz Montiaceae Synopsis of a new taxonomic synthesis of Montiaceae (Portulacineae) based on rational metadata analysis, with critical new insights on historically poorly understood taxa and a review of ecological evolution and phylogeography Mark Alan HERSHKOVITZ1 1Santiago, Chile [email protected] Abstract: Montiaceae (Portulacineae) comprise a clade of at least 280 species and ca. 30 subspecific taxa primarily of western America and Australia. This work uses existing phylogenetic metadata to elaborate a new cladistic taxonomic synthesis, and clarifies morphological circumscriptions of several poorly known species. A total of 20 taxa are validated, seven new and 13 necessary nomenclatural recombinations. Hypotheses of Montiaceae historical biogeography and phenotypic evolution are evaluated in light of recent metadata. Key words: Montiaceae, taxonomy, phylogeny, ecology, phylogeography, evolution. 1. Introduction This work presents a new cladistic taxonomy of Montiaceae (Portulacineae) and several of its included taxa, along with notes on the diagnostics of certainly poorly known species and a summary of new interpretations of phylogeography and phenotypic and ecological evolution. The present work includes 20 nomenclatural novelties. However, the whole of the novelty is greater than the sum of these parts. The generic circumscriptions and diversity estimates are modified from Hernández-Ledesma et al. (2015).The suprageneric taxonomy is the first proposed since McNeill (1974) and the only phylogenetic one. Critical reevaluation of certain common and usually misidentified Chilean taxa is the first since Reiche (1898). Existing metadata are interpreted as evidence for a hybrid origin of a genus. -
The PDF, Here, Is a Full List of All Mentioned
FAUNA Vernacular Name FAUNA Scientific Name Read more a European Hoverfly Pocota personata https://www.naturespot.org.uk/species/pocota-personata a small black wasp Stigmus pendulus https://www.bwars.com/wasp/crabronidae/pemphredoninae/stigmus-pendulus a spider-hunting wasp Anoplius concinnus https://www.bwars.com/wasp/pompilidae/pompilinae/anoplius-concinnus a spider-hunting wasp Anoplius nigerrimus https://www.bwars.com/wasp/pompilidae/pompilinae/anoplius-nigerrimus Adder Vipera berus https://www.woodlandtrust.org.uk/trees-woods-and-wildlife/animals/reptiles-and-amphibians/adder/ Alga Cladophora glomerata https://en.wikipedia.org/wiki/Cladophora Alga Closterium acerosum https://www.algaebase.org/search/species/detail/?species_id=x44d373af81fe4f72 Alga Closterium ehrenbergii https://www.algaebase.org/search/species/detail/?species_id=28183 Alga Closterium moniliferum https://www.algaebase.org/search/species/detail/?species_id=28227&sk=0&from=results Alga Coelastrum microporum https://www.algaebase.org/search/species/detail/?species_id=27402 Alga Cosmarium botrytis https://www.algaebase.org/search/species/detail/?species_id=28326 Alga Lemanea fluviatilis https://www.algaebase.org/search/species/detail/?species_id=32651&sk=0&from=results Alga Pediastrum boryanum https://www.algaebase.org/search/species/detail/?species_id=27507 Alga Stigeoclonium tenue https://www.algaebase.org/search/species/detail/?species_id=60904 Alga Ulothrix zonata https://www.algaebase.org/search/species/detail/?species_id=562 Algae Synedra tenera https://www.algaebase.org/search/species/detail/?species_id=34482