Redalyc.Distinguishing Colour Variants of Serapias Perez-Chiscanoi
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Morphological Systematics of Serapias L.(Orchidaceae) in Southwest
Pl. Syst. Evol. 265: 165–177 (2007) Plant Systematics DOI 10.1007/s00606-007-0519-0 and Evolution Printed in The Netherlands Morphological systematics of Serapias L. (Orchidaceae) in Southwest Europe C. Venhuis, P. Venhuis, J. G. B. Oostermeijer, and P. H. van Tienderen Institute for Biodiversity and Ecosystem Dynamics, Universiteit van Amsterdam, Amsterdam, The Netherlands Received January 27, 2006; accepted January 18, 2007 Published online: April 30, 2007 Ó Springer-Verlag 2007 Abstract. We measured morphological characters while Sundermann (1980) only mentioned and relative DNA contents to assess variation and three. The distribution is predominantly Med- phylogenetic relationships among Serapias species in iterranean. Its range extends from the Azores three populations of each of the 10 putative taxa that and the Canaries in the west to the Caucasus in occur in Southwest Europe. DNA contents indicated the east, and as far north as Brittany (France) diploidy for most species, except for tetraploid S. (Go¨lz and Reinhard 1980; Perez Chiscano lingua and hexaploid S. olbia. Multivariate (discrimi- et al. 1991; Delforge 1995, 2002). The genus nant) analyses yielded two main groups: a small- flowered S. parviflora group and a large-flowered is considered monophyletic, based on genetic S. vomeracea group. Within the S. parviflora group, S. (Pridgeon et al. 1997; Bateman et al. 1997, elsae should be considered a large-flowered variation 2003) and morphological differences (Delforge of S. strictiflora. The geographically disjunct S. gre- 1995, 2002). Serapias is represented in south- garia and S. strictiflora are probably different taxa. In west Europe (Iberian Peninsula and southern the S. -
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. -
Metacommunities and Biodiversity Patterns in Mediterranean Temporary Ponds: the Role of Pond Size, Network Connectivity and Dispersal Mode
METACOMMUNITIES AND BIODIVERSITY PATTERNS IN MEDITERRANEAN TEMPORARY PONDS: THE ROLE OF POND SIZE, NETWORK CONNECTIVITY AND DISPERSAL MODE Irene Tornero Pinilla Per citar o enllaçar aquest document: Para citar o enlazar este documento: Use this url to cite or link to this publication: http://www.tdx.cat/handle/10803/670096 http://creativecommons.org/licenses/by-nc/4.0/deed.ca Aquesta obra està subjecta a una llicència Creative Commons Reconeixement- NoComercial Esta obra está bajo una licencia Creative Commons Reconocimiento-NoComercial This work is licensed under a Creative Commons Attribution-NonCommercial licence DOCTORAL THESIS Metacommunities and biodiversity patterns in Mediterranean temporary ponds: the role of pond size, network connectivity and dispersal mode Irene Tornero Pinilla 2020 DOCTORAL THESIS Metacommunities and biodiversity patterns in Mediterranean temporary ponds: the role of pond size, network connectivity and dispersal mode IRENE TORNERO PINILLA 2020 DOCTORAL PROGRAMME IN WATER SCIENCE AND TECHNOLOGY SUPERVISED BY DR DANI BOIX MASAFRET DR STÉPHANIE GASCÓN GARCIA Thesis submitted in fulfilment of the requirements to obtain the Degree of Doctor at the University of Girona Dr Dani Boix Masafret and Dr Stéphanie Gascón Garcia, from the University of Girona, DECLARE: That the thesis entitled Metacommunities and biodiversity patterns in Mediterranean temporary ponds: the role of pond size, network connectivity and dispersal mode submitted by Irene Tornero Pinilla to obtain a doctoral degree has been completed under our supervision. In witness thereof, we hereby sign this document. Dr Dani Boix Masafret Dr Stéphanie Gascón Garcia Girona, 22nd November 2019 A mi familia Caminante, son tus huellas el camino y nada más; Caminante, no hay camino, se hace camino al andar. -
“Dynamic Speciation Processes in the Mediterranean Orchid Genus Ophrys L
“DYNAMIC SPECIATION PROCESSES IN THE MEDITERRANEAN ORCHID GENUS OPHRYS L. (ORCHIDACEAE)” Tesi di Dottorato in Biologia Avanzata, XXIV ciclo (Indirizzo Sistematica Molecolare) Universitá degli Studi di Napoli Federico II Facoltá di Scienze Matematiche, Fisiche e Naturali Dipartimento di Biologia Strutturale e Funzionale 1st supervisor: Prof. Salvatore Cozzolino 2nd supervisor: Prof. Serena Aceto PhD student: Dott. Hendrik Breitkopf 1 Cover picture: Pseudo-copulation of a Colletes cunicularius male on a flower of Ophrys exaltata ssp. archipelagi (Marina di Lesina, Italy. H. Breitkopf, 2011). 2 TABLE OF CONTENTS GENERAL INTRODUCTION CHAPTER 1: MULTI-LOCUS NUCLEAR GENE PHYLOGENY OF THE SEXUALLY DECEPTIVE ORCHID GENUS OPHRYS L. (ORCHIDACEAE) CHAPTER 2: ANALYSIS OF VARIATION AND SPECIATION IN THE OPHRYS SPHEGODES SPECIES COMPLEX CHAPTER 3: FLORAL ISOLATION IS THE MAIN REPRODUCTIVE BARRIER AMONG CLOSELY RELATED SEXUALLY DECEPTIVE ORCHIDS CHAPTER 4: SPECIATION BY DISTURBANCE: A POPULATION STUDY OF CENTRAL ITALIAN OPHRYS SPHEGODES LINEAGES CONTRIBUTION OF CO-AUTHORS ACKNOWLEDGEMENTS 3 GENERAL INTRODUCTION ORCHIDS With more than 22.000 accepted species in 880 genera (Pridgeon et al. 1999), the family of the Orchidaceae is the largest family of angiosperm plants. Recently discovered fossils document their existence for at least 15 Ma. The last common ancestor of all orchids has been estimated to exist about 80 Ma ago (Ramirez et al. 2007, Gustafsson et al. 2010). Orchids are cosmopolitan, distributed on all continents and a great variety of habitats, ranging from deserts and swamps to arctic regions. Two large groups can be distinguished: Epiphytic and epilithic orchids attach themselves with aerial roots to trees or stones, mostly halfway between the ground and the upper canopy where they absorb water through the velamen of their roots. -
A New Tongue-Orchid (Orchidaceae) in Southwest Spain: Serapias Occidentalis
Anales del Jardín Botánico de Madrid Vol. 63(2): 131-143 July-December 2006 ISSN: 0211-1322 A new Tongue-orchid (Orchidaceae) in southwest Spain: Serapias occidentalis by Caspar Venhuis, Pepijn Venhuis & Albertine C. Ellis-Adam Institute for Biodiversity and Ecosystem Dynamics (IBED), Universiteit van Amsterdam, Kruislaan 118, 1098 SM, Amsterdam, The Netherlands [email protected] Abstract Resumen Serapias occidentalis is described from several populations Se describe Serapias occidentalis a partir de diferentes poblacio- (Campo Lugar, Obando and Aljucén) scattered over the Gua- nes (Campo Lugar, Obando y Aljucén) situadas a lo largo de la diana river basin in Extremadura, Spain. Morphological charac- cuenca del río Guadiana en Extremadura, España. Se analizan ters defining the new species are analysed, and differences with los caracteres morfológicos que definen la nueva especie y sus related Serapias taxa from the Iberian Peninsula and other Euro- diferencias con otras Serapias de la Península Ibérica y de Euro- pean countries are established. In addition, distribution, ecology pa. Además, se discuten diversos aspectos de su distribución, and reproduction are discussed. hábitat y reproducción. Keywords: Orchidaceae, Serapias, taxonomy, Spain, Ex- Palabras clave: Orchidaceae, Serapias, taxonomía, España, Ex- tremadura. tremadura. Introduction 1991; Delforge, 1995b, 2002). Most recent studies, however, report several other Serapias species cover- The genus Serapias L. (Tongue-orchids) comprises ing large parts of this distribution area and suggest 26 species (Delforge, 2002), with a predominantly that at least parts of the populations previously con- Mediterranean distribution. Its range extends from sidered as S. vomeracea would, in fact, be representa- the Azores and the Canaries in the west to the Cauca- tives of those species. -
Taxonomic and Distributive Notes on Serapias Lingua Subsp. Tunetana (Orchidaceae), a Rare Endemic to Tunisia
Collectanea Botanica 38: e005 enero-diciembre 2019 ISSN-L: 0010-0730 https://doi.org/10.3989/collectbot.2019.v38.005 Taxonomic and distributive notes on Serapias lingua subsp. tunetana (Orchidaceae), a rare endemic to Tunisia R. EL MOKNI1,2,3 & G. DOMINA4 1 University of Carthage, Laboratory of Botany and Plant Ecology (SNA-214), Department of Life Sciences, Faculty of Sciences of Bizerte, Jarzouna, TN-7021 Bizerte, Tunisia 2 University of Jendouba, Laboratory of Silvo-pastoral Resources, Silvo-Pastoral Institute of Tabarka, BP. 345, TN-8110 Tabarka, Tunisia 3 University of Monastir, Laboratory of Botany, Cryptogamy and Plant Biology, Faculty of Pharmacy of Monastir, Avenue Avicenna, TN-5000 Monastir, Tunisia 4 University of Palermo, Department of Agriculture, Food and Forest Sciences, viale delle Scienze, bldg. 4, IT-90128 Palermo, Italy ORCID iD. R. EL MOKNI: https://orcid.org/0000-0003-3849-1039, G. DOMINA: https://orcid.org/0000-0003-4184-398X Author for correspondence: G. Domina ([email protected]) Editor: L. Sáez Received 10 August 2018; accepted 2 October 2018; published on line 6 May 2019 Abstract TAXONOMIC AND DISTRIBUTIVE NOTES ON SERAPIAS LINGUA SUBSP. TUNETANA (ORCHIDACEAE), A RARE ENDEMIC TO TUNISIA.— Serapias lingua subsp. tunetana, a rare endemic orchid confined to Tunis, northern of Tunisia, has been rediscovered far away from its type locality nearly after 22 years. Since its first finding in 1996 and its description published in 2005, the subspecies has not been found again, and was presumed to be extinct, or the taxon was erroneously identified. A detailed description of the subspecies justifying an amendment to its description, a map of its current distribution and colour photographs are also provided. -
Southern Maidenhair Fern and Stream Orchid in the Black Hills National Forest, South Dakota and Wyoming
United States Department of Agriculture Conservation Assessment Forest Service for Southern Maidenhair Rocky Mountain Region Fern and Stream Orchid in Black Hills National Forest the Black Hills National Custer, South Dakota Forest South Dakota and April 2003 Wyoming J.Hope Hornbeck, Deanna Reyher, Carolyn Hull Sieg and Reed W. Crook Species Assessment of Southern Maidenhair Fern and Stream Orchid in the Black Hills National Forest, South Dakota and Wyoming J. Hope Hornbeck, Deanna J. Reyher, Carolyn Hull Sieg and Reed W. Crook J. Hope Hornbeck is a Botanist with the Black Hills National Forest in Custer, South Dakota. She completed a B.S. in Environmental Biology at The University of Montana and a M.S. in Plant Biology at the University of Minnesota-Twin Cities. Deanna J. Reyher is an Ecologist/Soil Scientist with the Black Hills National Forest in Custer, South Dakota. She completed a B.S. degree in Agronomy from the University of Nebraska- Lincoln. Carolyn Hull Sieg is a Research Plant Ecologist with the Rocky Mountain Research Station in Flagstaff, Arizona. She completed a B.S. in Wildlife Biology and M.S. in Range Science from Colorado State University and a Ph.D. in Range and Wildlife Management at Texas Tech University. Reed W. Crook is a Botanist with the Black Hills National Forest in Custer, South Dakota. He completed a B.S. in Botany at Brigham Young University, a M.S. in Plant Morphology and Ph.D. in Plant Systematics at the University of Georgia-Athens. EXECUTIVE SUMMARY Southern maidenhair fern (Adiantum capillus-veneris L.; Pteridaceae) is a cosmopolitan species that is widely distributed in southern North America. -
Orchidaceae) by Imitation of Holes for Sleeping Solitary Male Bees (Hymenoptera
69-73. Acta Bot. Need. 30(1/2), February 1981, p. Pollination of Serapias vomeracea Briq. (Orchidaceae) by imitation of holes for sleeping solitary male bees (Hymenoptera) 1 2 3 Amots Dafni Yariv Ivri andN.B.M. Brantjes 1 Institute of Evolution, Haifa University, Mount Carmel, Haifa 31 999, Israel 2 Kibbutz Ayeleth Ha'shahar, Israel 3 Vakgroep Plantensystematiek, Biologisch Centrum, Postbus 14, 9750 AA Haren (Gn), The Netherlands SUMMARY In two locations in Israel, bees were found to be sleeping in flowers ofSerapias vomeracea Briq. Of these and Ceratina too small to bees. Proposis spp. spp. were be pollinators, whereas Eucera spp., Andrena spp., Osmia spp. and Tetralonia spp., mostly males, pollinated. Pollination occurs when in the afternoon hours the bees waver from flower to flower. The bees rest In finally come to on a particular flower and remain there for the duration of the night. the morning, the bees which slept in the flowers, are warmed up as aresult ofsolar radiation which heats the flowers to 3°C above ambient temperature. Since the males of many Hymenoptera sleepin holes,the hypothesisis that the flowers mimic such holes. The shortness of the flower tube can be held responsible for the observed frequent changes from flower to flower, which is so important for pollinationefficiency. 1. INTRODUCTION Serapias vomeracea Briq. is a Mediterranean species found in fertile meadows, heaths, and dampwoods, from sea level up to 1000m. altitude(Duperrex 1965). this in habitats all the Mediterranean In Israel, species appears damp open over territory, mainly in dwarf shrub communities (‘Batha’) and in marsh fringes, without showing preferences to any particular soil (Dafni 1979). -
(2008) Morphometric and Population Genetic Analyses
Botanical Journal of the Linnean Society, 2008, 157, 687–711. With 11 figures Morphometric and population genetic analyses elucidate the origin, evolutionary significance and conservation implications of Orchis ¥angusticruris (O. purpurea ¥ O. simia), a hybrid orchid new to Britain RICHARD M. BATEMAN*, RHIAN J. SMITH and MICHAEL F. FAY Jodrell Laboratory, Royal Botanic Gardens Kew, Richmond, Surrey TW9 3DS, UK Received 16 January 2008; accepted for publication 17 March 2008 We report the first confirmed occurrence in Britain of Orchis ¥ angusticruris Franch. ex Rouy, a hybrid between two closely related orchid species of anthropomorphic Orchis (O. purpurea Huds. ¥ O. simia Lam.) that hybridize frequently in Continental Europe. Seven individual hybrids, most likely F1 plants representing a single interspe- cific pollination event, first flowered with both parents in May 2006 at a nature reserve in the Chiltern Hills near Goring, Oxfordshire. Univariate and multivariate morphometric analyses (43 characters plus 12 indices), internal transcribed spacer sequencing, plastid microsatellites and amplified fragment length polymorphism (AFLP) analyses together readily separate the parents and confirm that O. purpurea was the ovule parent and O. simia the pollen parent, presumably reflecting the greater frequency and/or later flowering period of the latter at the site. This study reinforces a more general observation that, in most orchids, the ovule parent contributes substantially more to the hybrid phenotype than does the pollen parent, perhaps reflecting cytoplasmic inheritance. In contrast, the hybrids are placed closer to O. simia than to O. purpurea in the AFLP tree. Apparently recent arrivals, the few O. purpurea plants at Goring contrast genetically with the two other small populations of this species known in the Chilterns, but rather are consistent with relatively uncommon Continental populations. -
ZNIEFF Continentales : Liste Des Espèces De Flore Remarquables En Région PACA
Actualisation de l’inventaire des Zones Naturelles d’Intérêt Écologique, Faunistique et Floristique (ZNIEFF) de Provence-Alpes-Côte d’Azur ZNIEFF continentales : liste des espèces de flore remarquables en région PACA Version du 28/07/2016 Référentiel taxonomique : TAXREF v5.0 Les alismatales, apiales et asparagales PHYLUM CLASSE ORDRE FAMILLE CD_REF RANG NOM_VALIDE Plantae Equisetopsida Alismatales Alismataceae 81260 ES Alisma gramineum Lej., 1811 Plantae Equisetopsida Alismatales Cymodoceaceae 93774 ES Cymodocea nodosa (Ucria) Asch., 1869 Plantae Equisetopsida Alismatales Posidoniaceae 115222 ES Posidonia oceanica (L.) Delile, 1813 Plantae Equisetopsida Alismatales Potamogetonaceae 130599 ES Zannichellia palustris L., 1753 Plantae Equisetopsida Apiales Apiaceae 87074 ES Bupleurum odontites L., 1753 Plantae Equisetopsida Apiales Apiaceae 98032 ES Ferulago campestris (Besser) Grecescu, 1898 Plantae Equisetopsida Apiales Apiaceae 104456 ES Katapsuxis silaifolia (Jacq.) Raf., 1840 Plantae Equisetopsida Apiales Apiaceae 108739 ES Molopospermum peloponnesiacum (L.) W.D.J.Koch, 1824 Plantae Equisetopsida Apiales Apiaceae 113586 ES Pimpinella peregrina L., 1753 Plantae Equisetopsida Asparagales Amaryllidaceae 81358 ES Allium coppoleri Tineo, 1827 Plantae Equisetopsida Asparagales Amaryllidaceae 81525 ES Allium subhirsutum L., 1753 Plantae Equisetopsida Asparagales Amaryllidaceae 81537 ES Allium trifoliatum Cirillo, 1792 Plantae Equisetopsida Asparagales Amaryllidaceae 99233 ES Galanthus nivalis L., 1753 Plantae Equisetopsida Asparagales Amaryllidaceae -
Orchidoideae: Orchidaceae) Author(S): H
The Phylogeny and Classification of the Diseae (Orchidoideae: Orchidaceae) Author(s): H. P. Linder and H. Kurzweil Source: Annals of the Missouri Botanical Garden, Vol. 81, No. 4 (1994), pp. 687-713 Published by: Missouri Botanical Garden Press Stable URL: http://www.jstor.org/stable/2399916 Accessed: 27-07-2016 11:10 UTC Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at http://about.jstor.org/terms JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. Missouri Botanical Garden Press is collaborating with JSTOR to digitize, preserve and extend access to Annals of the Missouri Botanical Garden This content downloaded from 137.158.114.36 on Wed, 27 Jul 2016 11:10:19 UTC All use subject to http://about.jstor.org/terms THE PHYLOGENY AND H. P. Linder2 and H. Kurzweil2'3 CLASSIFICATION OF THE DISEAE (ORCHIDOIDEAE: ORCHIDACEAE)l ABSTRACT The subtribal classification of the Diseae (Orchidoideae) is reviewed in light of the available morphological, leaf anatomical, and palynological data. These data are critically assessed, and the more prominent features are illustrated. The data are analyzed cladistically, and the robustness of the various components of the most parsimonious tree is assessed by a bootstrap analysis. Based on the cladistic analysis and the bootstrap analysis, a new classification is proposed for the Diseae. -
Pdf of JHOS July 2004
JOURNAL of the HARDY ORCHID SOCIETYVoI. 1 No. 3 (33) - July 2004 The Hardy Orchid Society Our aim is to promote interest in the study of Native European Orchids and those from similar temperate climates throughout the world. We cover such varied aspects as field study, cultivation and propagation, photography, taxonomy and systematics, and prac- conservation. We tical welcome articles relating to any of these subjects, which will be ! considered for publication by the editorial committee. Please send your submissions to the Editor, and please structure your text according to the 'Advice for Authors' (see website, January 2004 journal or contact the editor). The Hardy Orchid Society Committee is .... President: Vacant. Chairman: Tony Hughes, 8 Birchwood Road, Malvem, Worcs, WR14 1LD. tonyhughes3 @ btinternet. com. Yice-Chairman: Vacant. Hon. Secretary: Chris Birchall, Barratts Cottage, Clyst Hydon, Cullompton, Devon EX1 5 2NQ. chris. s.birchall @ tesco.net. Hon.Treasurer: Rosemary Hin, 38 Springfield Crescent, Harpenden, Herts, AL5 4LH. [email protected]. Membership Secretary: Maren Talbot, 4 Hazel Close, Marlow, Bucks, SL7 3PVf. mtalbot @ onetel.net.uk. Show Secretary: Eric Webster, 25 Highfields Drive, Loughborough, LBl1 3JS. [email protected]. Journal Editor: Patrick Marks, 40 Lawmill Gardens, St.Andrews, Fife KY16 8QS. [email protected][freeret or Conservation Officer: Bill Temple, Primrose Cottage, Hanney Road, Steventon, Oxon, OXI 3 6AP. bill @[email protected]. Publicity Officer: Jim Hill, 38 Springfield Crescent, Haqpenden, Herts, AL5 4LH. [email protected]. Ordinary Member (Seed and Fungus Bank): Ted Weeks, 74 Over Lane, Almondsbury Bristol, BS32 4BT. Wecw394 1 @ aol.com. Ordinary Member (Newsletter Distribution): Barry Tattersall, 262 Staines Road, Twickenham, Middlesex, TW2 5AR.