Madeira - the Floating Garden
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Cally Plant List a ACIPHYLLA Horrida
Cally Plant List A ACIPHYLLA horrida ACONITUM albo-violaceum albiflorum ABELIOPHYLLUM distichum ACONITUM cultivar ABUTILON vitifolium ‘Album’ ACONITUM pubiceps ‘Blue Form’ ACAENA magellanica ACONITUM pubiceps ‘White Form’ ACAENA species ACONITUM ‘Spark’s Variety’ ACAENA microphylla ‘Kupferteppich’ ACONITUM cammarum ‘Bicolor’ ACANTHUS mollis Latifolius ACONITUM cammarum ‘Franz Marc’ ACANTHUS spinosus Spinosissimus ACONITUM lycoctonum vulparia ACANTHUS ‘Summer Beauty’ ACONITUM variegatum ACANTHUS dioscoridis perringii ACONITUM alboviolaceum ACANTHUS dioscoridis ACONITUM lycoctonum neapolitanum ACANTHUS spinosus ACONITUM paniculatum ACANTHUS hungaricus ACONITUM species ex. China (Ron 291) ACANTHUS mollis ‘Long Spike’ ACONITUM japonicum ACANTHUS mollis free-flowering ACONITUM species Ex. Japan ACANTHUS mollis ‘Turkish Form’ ACONITUM episcopale ACANTHUS mollis ‘Hollard’s Gold’ ACONITUM ex. Russia ACANTHUS syriacus ACONITUM carmichaelii ‘Spätlese’ ACER japonicum ‘Aconitifolium’ ACONITUM yezoense ACER palmatum ‘Filigree’ ACONITUM carmichaelii ‘Barker’s Variety’ ACHILLEA grandifolia ACONITUM ‘Newry Blue’ ACHILLEA ptarmica ‘Perry’s White’ ACONITUM napellus ‘Bergfürst’ ACHILLEA clypeolata ACONITUM unciniatum ACIPHYLLA monroi ACONITUM napellus ‘Blue Valley’ ACIPHYLLA squarrosa ACONITUM lycoctonum ‘Russian Yellow’ ACIPHYLLA subflabellata ACONITUM japonicum subcuneatum ACONITUM meta-japonicum ADENOPHORA aurita ACONITUM napellus ‘Carneum’ ADIANTUM aleuticum ‘Japonicum’ ACONITUM arcuatum B&SWJ 774 ADIANTUM aleuticum ‘Miss Sharples’ ACORUS calamus ‘Argenteostriatus’ -
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African countries and neighbouring islands covered by the Synopsis. S T R E L I T Z I A 23 Synopsis of the Lycopodiophyta and Pteridophyta of Africa, Madagascar and neighbouring islands by J.P. Roux Pretoria 2009 S T R E L I T Z I A This series has replaced Memoirs of the Botanical Survey of South Africa and Annals of the Kirstenbosch Botanic Gardens which SANBI inherited from its predecessor organisations. The plant genus Strelitzia occurs naturally in the eastern parts of southern Africa. It comprises three arborescent species, known as wild bananas, and two acaulescent species, known as crane flowers or bird-of-paradise flowers. The logo of the South African National Biodiversity Institute is based on the striking inflorescence of Strelitzia reginae, a native of the Eastern Cape and KwaZulu-Natal that has become a garden favourite worldwide. It sym- bolises the commitment of the Institute to champion the exploration, conservation, sustain- able use, appreciation and enjoyment of South Africa’s exceptionally rich biodiversity for all people. J.P. Roux South African National Biodiversity Institute, Compton Herbarium, Cape Town SCIENTIFIC EDITOR: Gerrit Germishuizen TECHNICAL EDITOR: Emsie du Plessis DESIGN & LAYOUT: Elizma Fouché COVER DESIGN: Elizma Fouché, incorporating Blechnum palmiforme on Gough Island PHOTOGRAPHS J.P. Roux Citing this publication ROUX, J.P. 2009. Synopsis of the Lycopodiophyta and Pteridophyta of Africa, Madagascar and neighbouring islands. Strelitzia 23. South African National Biodiversity Institute, Pretoria. ISBN: 978-1-919976-48-8 © Published by: South African National Biodiversity Institute. Obtainable from: SANBI Bookshop, Private Bag X101, Pretoria, 0001 South Africa. -
Proceedings Amurga Co
PROCEEDINGS OF THE AMURGA INTERNATIONAL CONFERENCES ON ISLAND BIODIVERSITY 2011 PROCEEDINGS OF THE AMURGA INTERNATIONAL CONFERENCES ON ISLAND BIODIVERSITY 2011 Coordination: Juli Caujapé-Castells Funded and edited by: Fundación Canaria Amurga Maspalomas Colaboration: Faro Media Cover design & layout: Estudio Creativo Javier Ojeda © Fundación Canaria Amurga Maspalomas Gran Canaria, December 2013 ISBN: 978-84-616-7394-0 How to cite this volume: Caujapé-Castells J, Nieto Feliner G, Fernández Palacios JM (eds.) (2013) Proceedings of the Amurga international conferences on island biodiversity 2011. Fundación Canaria Amurga-Maspalomas, Las Palmas de Gran Canaria, Spain. All rights reserved. Any unauthorized reprint or use of this material is prohibited. No part of this book may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, or by any information storage and retrieval system without express written permission from the author / publisher. SCIENTIFIC EDITORS Juli Caujapé-Castells Jardín Botánico Canario “Viera y Clavijo” - Unidad Asociada CSIC Consejería de Medio Ambiente y Emergencias, Cabildo de Gran Canaria Gonzalo Nieto Feliner Real Jardín Botánico de Madrid-CSIC José María Fernández Palacios Universidad de La Laguna SCIENTIFIC COMMITTEE Juli Caujapé-Castells, Gonzalo Nieto Feliner, David Bramwell, Águedo Marrero Rodríguez, Julia Pérez de Paz, Bernardo Navarro-Valdivielso, Ruth Jaén-Molina, Rosa Febles Hernández, Pablo Vargas. Isabel Sanmartín. ORGANIZING COMMITTEE Pedro -
Morphological Nature of Floral Cup in Lauraceae
l~Yoc. Indian Acad. Sci., Vol. 88 B, Part iI, Number 4, July 1979, pp. 277-281, @ printed in India. Morphological nature of floral cup in Lauraceae S PAL School of Plant Morphology, Meerut College, Meerut 250 001 MS received 19 June 1978 Abstract. On the basis of anatomical criteria the floral cup of Lauraceae can be regarded as appendicular, as the traces entering into the floral cup are morphologi- cally compound, differentiated into tepal and stamen traces at higher levels. The ontogenetic studies also support this contention. The term Perigynous hypanthium is retained for the floral cup of Lauraceae as it is formed as a result of intercalary growth occurring underneath the region of perianth and androecium. Keywords. Lauraceae; floral cup; morphological nature; appendicular; peri- gynous hypanthium. 1. Introduction The family Lauraceae has received comparatively little attention from earlier workers because of difficulty in procuring the material. So far very little work has been done on the floral anatomy of this family (Reece 1939 ; Sastri 1952 ; Pal 1974). There has been considerable difference of opinion regarding the nature of floral cup in angiosperms. The present work was initiated to study the morphological nature of the floral cup. 2. Materials and methods The present investigation embodies the results of observations on 21 species of the Lauraceae. The material of Machilus duthiei King ex Hook.f., M. odoratissima Nees, Persea gratissima Gaertn.f., Phoebe cooperiana Kanjilal and Das, P. goal- parensis Hutch., P. hainesiana Brandis, Alseodaphne keenanii Gamble, A. owdeni Parker, Cinnamomum camphora Nees and Eberm, C. cecidodaphne Meissn., C. tamala Nees and Eberm, C. -
Portugal – Madeira 2017
Madeira 8–12 July 2017 Pelagic Extension to 15 July Participants John Thorogood Brian Roberts-Wray Emma Rees-Wray Massimiliano Dettori James and Vivienne Harvey Frederick Alway Bahar Bilgen William Dixon Robin Griffiths Leaders Catarina Correia-Fagundes and Hugo Romano Trocaz Pigeon Day 1 Most of the group arrived at Madeira’s airport around 19:30 after a 40-minutes delay on the flight schedule and our guides were waiting for us outside the baggage claim to take us to the hotel. The drive to the hotel was only five minutes and after check-in we had dinner and a nice rest after it. Day 2 We started the day visiting the most arid area in Madeira, on the eastern tip, Ponta de São Lourenço, where we watched Berthelot’s Pipits, Eurasian Kestrels and Clouded Yellow Butterflies. We only had a glimpse of two Rock Petronias flying and sitting on a rock for less than 20 seconds which did not allow everyone to have a good look at them through the telescope. Then we drove to the centre of the village of Caniçal where we looked for Spanish Sparrows and where a male displayed quite well. A male Blackcap and Eurasian Collared- doves were also observed here. After we headed to the north side of the island, to Faial, in search for the endemic Trocaz Pigeon and where we were very successful watching a few flying and others sitting on branches on open view. Lunch was taken at a restaurant with a really nice view over the green cliffs diving into the blue of the ocean and from where we saw more Eurasian Kestrels and Trocaz Pigeons flying and a Eurasian Sparrowhawk. -
The Occurrence of Red and Yellow Autumn Leaves Explained by Regional Differences in Insolation and Temperature
Review Tansley review The occurrence of red and yellow autumn leaves explained by regional differences in insolation and temperature Authors for correspondence: Susanne S. Renner1 and Constantin M. Zohner2 Susanne S. Renner 1 2 Tel: +49 89 17861 250 Systematic Botany and Mycology, University of Munich (LMU), Menzinger Str. 67, Munich 80638, Germany ; Institute of Email: [email protected] Integrative Biology, Department of Environmental Systems Science, ETH Zurich, Zurich 8092, Switzerland Constantin M. Zohner Email: [email protected] Received: 19 January 2019 Accepted: 24 April 2019 Contents Summary 1464 IV. The adaptive value of colour-changing leaves 1468 I. Introduction 1464 V. Outlook 1469 II. Phylogenetic and geographical occurrence of autumn colour Acknowledgements 1469 change 1465 References 1470 III. Physiological functions of autumnal leaf xanthophylls and anthocyanins 1466 Summary New Phytologist (2019) 224: 1464–1471 Red or yellow autumn leaves have long fascinated biologists, but their geographical doi: 10.1111/nph.15900 concentration in trees in Eastern North America (ENA) has defied evolutionary explanations. In this review, anthocyanins and xanthophylls are discussed in relation to their occurrence in Key words: adaptive explanation, different regions of the Northern Hemisphere, phylogenetic distribution and photoprotective anthocyanins, photo-oxidative damage, function during the breakdown of chlorophylls. Pigments in senescing leaves that intercept regional climates, solar irradiation, incident light and dissipate the absorbed energy extend the time available for nutrient resorption. xanthophylls. Experiments with Arabidopsis have revealed greatest anthocyanin photoprotective function at low temperatures and high light intensities, and high-resolution solar irradiation maps reveal that ENA and Asia receive higher irradiation than does Europe. -
Canary Islands, Spain
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Stapfia Jahr/Year: 2013 Band/Volume: 0099 Autor(en)/Author(s): van den Boom P.P.G. Artikel/Article: Further New or Interesting Lichens and Lichenicolous Fungi of Tenerife (Canary Islands, Spain) 52-60 © Biologiezentrum Linz/Austria; download unter www.biologiezentrum.a VAN DEN BOOM • New lichens and lichenicolous fungi from Tenerife STAPFIA 99 (2013): 52–60 Further New or Interesting Lichens and Lichenicolous Fungi of Tenerife (Canary Islands, Spain) P.P.G. VAN DEN BOOM* Abstract: In the presented annotated list, 88 taxa of lichens and lichernicolous fungi are additional records for the island Tenerife, of which 19 are new to the Canary Islands: Abrothallus aff. secedens, Anisomeridium robusta, Arthonia elegans, Buellia abstracta, B. fusca, Caloplaca phlogina, Endococcus pseudocarpus, Lecania brunonis, Lecanographa lyncea, Lecanora persimilis, L. subsaligna, Physcia atrostriata, P. sore- diosa, Plectocarpon nashii, Porina hoehneliana, Protopannaria pezizoides, Sarcopyrenia bacillosa, Scoli- ciosporum gallurae and Toninia talparum. Furthermore Bacidina pseudoisidiata and Micarea canariensis are newly described. Zusammenfassung: Eine annotierte Liste von 88 Flechten und lichenikolen Pilzen wird präsentiert mit wei- teren Funden für die Insel Teneriffa, von denen 19 neu für die Kanarischen Inseln sind: Abrothallus secedens, Anisomeridium robusta, Arthonia elegans, Buellia abstracta, B. fusca, Caloplaca phlogina, Endococcus pseudocarpus, Lecania brunonis, Lecanographa lyncea, Lecanora persimilis, L. subsaligna, Physcia atros- triata, P. sorediosa, Plectocarpon nashii, Porina hoehneliana, Protopannaria pezizoides, Sarcopyrenia bacil- losa, Scoliciosporum gallurae und Toninia talparum. Weiters werden Bacidina pseudoisidiata und Micarea canariensis neu beschrieben. Key words: diversity in lichens and lichenicolous fungi, new species, new records, ecology, Macaronesia. -
MADEIRA Itinerary 24-08 Arrived, and Put “My Girls” In
MADEIRA Great Shearwater by Catarina Romano This is a report of a family trip that got a bit “out of hand” for seeing some missing seabirds in the HA. The sites mentioned are easy to find at http://madeira.seawatching.net/ also good info on birds is to find on http://www.madeirabirds.com/+ http://www.venturadomar.com/ See also my report of 2001: http://77.167.75.191/doc/doc00129.pdf Itinerary 24-08 Arrived, and put “my girls” in the hotel and went for an evening seawatch (one and a half hours) to Porto Moniz to see a Great Shearwater within the first second.. 25-08 Seawatch from the hotel in the morning (near Ponta da Cruz (PC)) and evening at PC 26-08 Evening/night trip to the Pico Arriero 27-08 Trip with the Gaviao and Madeira Winds to the Desertas, very sick girls on the way up..(sorry..) 28-08 Seawatching at Porto Moniz for an hour in the evening while eating shrimp salad. Visited Ribero Janela on the way up. 29-08 Nothing special, except the usual Funchal harbor watch like every morning 30-08 Ponta da Cruz in the morning for a seawatch. 31-08 Porto Moniz in the evening for a one and a half hour seawatch 01-09 Trip to the Desertas with the Ventura do mar spending the night there first on the island and later on the deck of the boat hearing the seabirds all night. 02-09 Returning trip from the Desertas arriving just past one giving an interview to a local TV station 03-09 In the evening a Mountain trip to Ribero Frio 04-09 In the morning again to Ribero Frio and later on to Pico de Noguiera. -
1 Exotic Tree List Tree Number Botanical Name Afrikaanse Naam
Exotic tree list Tree Botanical Name Afrikaanse Naam English Name Origin Number X58 Abies concolor Witden White Fir N.Amer X59 Abies magnifica Rooiden Red Fir N.Amer X60 Abies nordmanniana Kaukasiese Den Caucasian Fir Turkey, Iran X61 Abies pinsapo Spaanse Den Spanish Fir Spain X62 Abies procera Edelden Noble Fir N.Amer Raspberry X486 Acacia acuminata Frambosewattel Aust Wattle X487 Acacia baileyana Bailey-se-wattel Bailey's Wattle Aust Knife-leaved X488 Acacia cultriformis Mesblaarwattel Aust Wattle X489 Acacia cyclops Rooikrans Red Eye Aust X490 Acacia dealbata Silwerwattel Silver Wattle Aust X491 Acacia decurrens Groenwattel Green Wattle Aust Gossamer X492 Acacia floribunda Spinnerakwattel Aust Wattle X493 Acacia longifolia Bleekwattel Sallow Wattle Aust X494 Acacia mearnsii Swartwattel Black Wattle Aust X495 Acacia melanoxylon Swarthout Blackwood Aust X496 Acacia pendula Treurwattel Weeping Myall Aust X497 Acacia podalyriifolia Vaalmimosa Pearl Acacia Aust X498 Acacia pycnantha Gouewattel Golden Wattle Aust Port Jackson X499 Acacia saligna Goudwilger Aust Willow Peppertree X500 Acacia terminalis Peperboomwattel Aust Wattle X658 Acer buergerianum Chinese Ahorn Chinese Maple China X659 Acer campestre Veldahorn Field Maple Eur, Turk, Iran X660 Acer circinatum Wingerdahorn Vine Maple N Amer Ash-leaved X661 Acer negundo Essenblaarahorn N & C Amer Maple X662 Acer palmatum Japanse Ahorn Japanese Maple Japan, China X663 Acer platanoides Noorse Ahorn Norway Maple Eur, Turk, Iran X664 Acer pseudo-platanus Valsplataan Sycamore Maple Eur, Asia -
The Laurel Or Bay Forests of the Canary Islands
California Avocado Society 1989 Yearbook 73:145-147 The Laurel or Bay Forests of the Canary Islands C.A. Schroeder Department of Biology, University of California, Los Angeles The Canary Islands, located about 800 miles southwest of the Strait of Gibraltar, are operated under the government of Spain. There are five islands which extend from 15 °W to 18 °W longitude and between 29° and 28° North latitude. The climate is Mediterranean. The two eastern islands, Fuerteventura and Lanzarote, are affected by the Sahara Desert of the mainland; hence they are relatively barren and very arid. The northeast trade winds bring moisture from the sea to the western islands of Hierro, Gomera, La Palma, Tenerife, and Gran Canaria. The southern ends of these islands are in rain shadows, hence are dry, while the northern parts support a more luxuriant vegetation. The Canary Islands were prominent in the explorations of Christopher Columbus, who stopped at Gomera to outfit and supply his fleet prior to sailing "off the map" to the New World in 1492. Return voyages by Columbus and other early explorers were via the Canary Islands, hence many plants from the New World were first established at these points in the Old World. It is suspected that possibly some of the oldest potato germplasm still exists in these islands. Man exploited the islands by growing sugar cane, and later Mesembryanthemum crystallinum for the extraction of soda, cochineal cactus, tomatoes, potatoes, and finally bananas. The banana industry is slowly giving way to floral crops such as strelitzia, carnations, chrysanthemums, and several new exotic fruits such as avocado, mango, papaya, and carambola. -
Documento Informativo RESERVA NATURAL ESPECIAL DE PUNTALLANA PLAN DIRECTOR
P la n D ir e c to r Reserva Natural Especial de APROBACIÓN APROBACIPuntallanaÓN DEFINITIVA DDEFINITIVA oc um en to In fo rm at ivo RESERVA NATURAL ESPECIAL DE PUNTALLANA PLAN DIRECTOR INDICE DOCUMENTO INFORMATIVO 1. DESCRIPCIÓN DE LA RESERVA NATURAL ESPECIAL .................................. 3 1.1 INTRODUCCIÓN ...................................................................................... 3 1.2 MEDIO FÍSICO............................................................................................ 3 1.2.1. Situación geográfica y extensión..................................................... 3 1.2.2. Clima ............................................................................................. 3 1.2.3. Geología y geomorfología ............................................................. 4 1.2.4. Características morfológicas .......................................................... 7 1.2.5. Hidrología ....................................................................................... 8 1.2.6. Edafología ..................................................................................... 10 1.2.7. Paisaje. Unidades de paisaje ....................................................... 12 1.3 MEDIO BIOLÓGICO ................................................................................. 14 1.3.1. Flora y vegetación ......................................................................... 14 1.3.2. Fauna ............................................................................................ 23 1.3.3. Medio litoral ................................................................................ -
Persea, Lauraceae
Scientific article doi: http://dx.doi.org/10.5154/r.rchsh.2017.12.038 Phylogenetic analysis of some members of the subgenus Persea (Persea, Lauraceae) Análisis filogenético de algunos miembros del subgénero Persea (Persea, Lauraceae) María Edith Cruz-Maya1; Alejandro Facundo Barrientos-Priego1*; Lily Xochitl Zelaya-Molina2; José Luis Rodríguez-de la O1; Juan Carlos Reyes-Alemán3 1Universidad Autónoma Chapingo, Departamento de Fitotecnia. Carretera México-Texcoco km 38.5, Texcoco, Estado de México, C. P. 56230, MÉXICO. 2Instituto Nacional de Investigaciones Forestales, Agrícolas y Pecuarias, Centro Nacional de Recursos Genéticos. Av. Biodiversidad núm. 2498, col. Centro, Tepatitlán de Morelos, Jalisco, C. P. 47600, MÉXICO. 3Universidad Autónoma del Estado de México. Carretera Tenancingo-Villa Guerrero km 1.5, Tenancingo, Estado de México, C. P. 52400, MÉXICO. *Corresponding author: [email protected]. Abstract he avocado belongs to the genus Persea, which is one of the most controversial genera of the Lauraceae family, since the relationships within the subgenus Persea are not clear T and only recognized two species, Persea americana and Persea schiedeana. Its relationship with the subgenus Eriodaphne is also complex and there is a debate as to whether it is an independent genus. For this reason, the study aims to analyze the phylogenetic relationships within the genus Persea, with an emphasis on the subgenus Persea, using maximum parsimony and bayesian inference with the sequence of eight different fragments from nuclear, chloroplast and mitochondrial DNA. Sequences of the chloroplast ndhF, rbcL, matK, rpoC, trnH- psbA; mitochondria atp4 and cox3 and nuclear 18S rRNA were used. Fourteen fixed mutations were found in species of the subgenus Eriodaphne.