COUNCIL Thirtieth Ordinary Session Geneva, October 23, 1996
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Phylogeny and Evolution of the Arctium-Cousinia Complex (Compositae, Cardueae-Carduinae)
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Digital.CSIC TAXON 58 (1) • February 2009: 153–171 López-Vinyallonga & al. • Arctium-Cousinia complex Phylogeny and evolution of the Arctium-Cousinia complex (Compositae, Cardueae-Carduinae) Sara López-Vinyallonga1,4*, Iraj Mehregan2,4, Núria Garcia-Jacas1, Olga Tscherneva3, Alfonso Susanna1 & Joachim W. Kadereit2 1 Botanical Institute of Barcelona (CSIC-ICUB), Pg. del Migdia s. n., 08038 Barcelona, Spain. *slopez@ibb. csic.es (author for correspondence) 2 Johannes Gutenberg-Universität Mainz, Institut für Spezielle Botanik und Botanischer Garten, 55099 Mainz, Germany 3 Komarov Botanical Institute, Ul. Prof. Popova 2, 197376 St. Petersburg, Russia 4 These authors contributed equally to this publication The phylogeny and evolution of the Arctium-Cousinia complex, including Arctium, Cousinia as one of the largest genera of Asteraceae, Hypacanthium and Schmalhausenia, is investigated. This group of genera has its highest diversity in the Irano-Turanian region and the mountains of Central Asia. We generated ITS and rpS4-trnT-trnL sequences for altogether 138 species, including 129 (of ca. 600) species of Cousinia. As found in previous analyses, Cousinia is not monophyletic. Instead, Cousinia subgg. Cynaroides and Hypacanthodes with together ca. 30 species are more closely related to Arctium, Hypacanthium and Schmalhausenia (Arc- tioid clade) than to subg. Cousinia (Cousinioid clade). The Arctioid and Cousiniod clades are also supported by pollen morphology and chromosome number as reported earlier. In the Arctioid clade, the distribution of morphological characters important for generic delimitation, mainly leaf shape and armature and morphology of involucral bracts, are highly incongruent with phylogenetic relationships as implied by the molecular data. -
Radiation in the Cape Flora and the Phylogeny of Peacock Irises Moraea
ARTICLE IN PRESS MOLECULAR PHYLOGENETICS AND EVOLUTION Molecular Phylogenetics and Evolution xxx (2002) xxx–xxx www.academicpress.com Radiation in the Cape flora and the phylogeny of peacock irises Moraea (Iridaceae) based on four plastid DNA regions Peter Goldblatt,a Vincent Savolainen,b,* Obie Porteous,b Ivan Sostaric,b Martyn Powell,b Gail Reeves,c John C. Manning,c Timothy G. Barraclough,d and Mark W. Chaseb a Missouri Botanical Garden, P.O. Box 299, St. Louis, Missouri 63166, USA b Molecular Systematics Section, Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond TW9 3DS, UK c National Botanical Institute, Kirstenbosch, Private Bag X7, Cape Town, South Africa d Department of Biology and NERC Centre for Population Biology, Imperial College, Silwood Park, Ascot, Berkshire SL5 7PY, UK Received 2 February 2002; received in revised form 22 April 2002 Abstract Phylogenetic analyses of four plastid DNA regions, the rbcL exon, trnL intron, trnL–trnF intergenic spacer, and rps16 intron from each of 73 species in the African genus Moraea (Iridaceae: Irideae) including accessions of all major species clusters in the genus, show Moraea to be paraphyletic when Barnardiella, Galaxia, Hexaglottis, Homeria (all southern African), and Gynandriris (Eurasian as well) were recognized as separate genera. There are several small, isolated species clusters at the basal nodes of the tree that are all restricted to the winter-rainfall zone of southern Africa (the Greater Cape floral kingdom) and a few, highly derived, large species groups that have radiated extensively within the winter-rainfall zone. Mapping of floral traits shows that an Iris-type flower is ancestral in Moraea. -
Mahonia × Media
Mahonia × media Mahonia × media is an interspecific hybrid shrub. Its parents are Mahonia oiwakensis subsp. lomariifolia (previously known as Mahonia lomariifolia) and Mahonia japonica. It was raised in gardens during the 20th Century, and has become an important garden and landscape plant. Description The hybrids show some variation, but are generally intermediate in most characteristics between the two parents. The following description is of the clone 'Charity'. These are medium to large shrubs, reaching 4 m (13 ft) in height. The plants have an upright form, becoming bare at the base. There are between 7 and 11 pairs of leaflets, plus a terminal leaflet. The flowers are in somewhat spreading racemes, often as long as in M. japonica. There is some scent to the flowers, but it is not as strong as in M. japonica. Flowering goes on throughout the winter. Different clones may resemble one or the other parent more closely. It is possible that other species of Mahonia have contributed to the stock ascribed to this hybrid. Mahonia bealei is considered particularly likely to be one of these as it is often confused with Mahonia japonica.Many clones have an upright architectural form derived from M. oiwakensis subsp. lomariifolia, though some resemble the M. japonica parent rather more. Plants provide viable seed, and second generation hybrids have been raised. The plants are especially valued in the garden because of their ornamental leaves, and because they flower through the winter. Origin The first recorded plant was found in a mixed batch of seedlings from Mahonia oiwakensis subsp. lomariifolia that was raised in Northern Ireland in 1951 or earlier. -
Report of a Working Group on Prunus: Sixth and Seventh Meetings
European Cooperative Programme for Plant Genetic Report of a Working Resources ECP GR Group on Prunus Sixth Meeting, 20-21 June 2003, Budapest, Hungary Seventh Meeting, 1-3 December 2005, Larnaca, Cyprus L. Maggioni and E. Lipman, compilers IPGRI and INIBAP operate under the name Bioversity International Supported by the CGIAR European Cooperative Programme for Plant Genetic Report of a Working Resources ECP GR Group on Prunus Sixth Meeting, 20 –21 June 2003, Budapest, Hungary Seventh Meeting, 1 –3 December 2005, Larnaca, Cyprus L. Maggioni and E. Lipman, compilers ii REPORT OF A WORKING GROUP ON PRUNUS: SIXTH AND SEVENTH MEETINGS Bioversity International is an independent international scientific organization that seeks to improve the well- being of present and future generations of people by enhancing conservation and the deployment of agricultural biodiversity on farms and in forests. It is one of 15 centres supported by the Consultative Group on International Agricultural Research (CGIAR), an association of public and private members who support efforts to mobilize cutting-edge science to reduce hunger and poverty, improve human nutrition and health, and protect the environment. Bioversity has its headquarters in Maccarese, near Rome, Italy, with offices in more than 20 other countries worldwide. The Institute operates through four programmes: Diversity for Livelihoods, Understanding and Managing Biodiversity, Global Partnerships, and Commodities for Livelihoods. The international status of Bioversity is conferred under an Establishment Agreement which, by January 2006, had been signed by the Governments of Algeria, Australia, Belgium, Benin, Bolivia, Brazil, Burkina Faso, Cameroon, Chile, China, Congo, Costa Rica, Côte d’Ivoire, Cyprus, Czech Republic, Denmark, Ecuador, Egypt, Greece, Guinea, Hungary, India, Indonesia, Iran, Israel, Italy, Jordan, Kenya, Malaysia, Mali, Mauritania, Morocco, Norway, Pakistan, Panama, Peru, Poland, Portugal, Romania, Russia, Senegal, Slovakia, Sudan, Switzerland, Syria, Tunisia, Turkey, Uganda and Ukraine. -
SIGNA: Species Iris Group of North America 31Th Species Seed Exchange
SIGNA: Species Iris Group of North America 1997 o 31th Species Seed Exchange Greetings: Orders will be filled in the order received. Return immediately for the best selection. Our first shipment of seeds will begin January 10. Orders received after that date will be filled as time permits. No orders will be filled if received after March 1, 1998. After each item in the seed list you will find a number estimating the total number of seeds available. Donations with fewer than 100 seeds will most likely be sold out early. Be sure to check substitutes when ordering any of these seeds. They will not be used as substitutes. Seeds in short supply may be packed with as few as 4 seeds. If you want items with more seeds per packet, order items in greater supply. Please note the following abreviations used in the seedlist: H P means Hand Pollinated, coli. means Wild Collected, and ex. indicates that the plants that seeds were collected from were originally from another source (which may be a person, another seed exchange, or a wild location) which immediately follows the abbreviation. The alphabetical groups (A, B, C, etc.) used in the seed list follow the outline provided in the SIGNA Species Iris Study Manual'publlshed in 1972, e.g. sub-section Pogoniris, series Pumilae is under A, sub-section Pogoniris, series Intermedeae in under B and so on. The Study Manual , The Iris by Brian Mathew, and Iris of China by James Waddick and Zhao Yu-tang are used as references when verifying names. -
Berberis (Zuurbes) En Mahonia (Mahonie)
bijenhouden 2010/11 - november # 16 Bijenplant belicht (slot) Berberis (zuurbes) en Mahonia (mahonie) 1 Berberis thunbergii ’Atropurpurea’ is een cultivar van de Japanse zuurbes; een fraaie vervanger van de inheemse Berberis vulgaris, die erg roestzwam gevoelig is Hennie Oude Essink nica (afb.2). Uit China is afkomstig de vormige verdikkingen aan de voet (afb.4); De Berberisfamilie (Berberidaceae) is al altijd groene Berberis julianae en uit dit zijn de nectarklieren, die ruim een zeer oud. In het stadje Florissant in de Noord-Amerika de reeds genoemde geurige nectar afscheiden. Hiertussen staat Colorado (Noord-Amerika) heeft men Mahonia aquifolium ook Berberis aquifoli - staan de zes meeldraden, elk vóór een een schat aan fossielen opgegraven, die um genoemd (stekelbladige mahonie; bloemblaadje. Als de bloem open gaat, een beeld geven van de flora en fauna daar afb.6). komen zij omhoog; bovenaan hebben zij, ter plekke van 34 miljoen jaren geleden. T-vormig, twee helmknoppen, die zo Ook de Berberis is daarbij: het betreft een Bloeiwijze en bloem draaien, dat de opening naar binnen is struik met blijvend groen blad, dat aan de De bloemen van de zuurbes en de mahonie gericht; via een klepje komt het pollen vrij. rand scherpe punten heeft, waarmee de kun je solitair aantreffen aan de overhan - Centraal in de bloem staat één stempel, plant zich beschermt tegen de toen over- gende twijgen van de plant maar door - zijnde een brede ring met kleverige haren; heersende planteneters. De soort is pas gaans staan zij in grote of kleine trossen zonder stijl staat hij op het bovenstandig zeer onlangs bij ons terecht gekomen; wij bijeen aan korte steeltjes vanuit de blad - vruchtbeginsel. -
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. -
Systematics of the Hypervariable Moraea Tripetalacomplex
Bothalia 42,2: 111– 135 (2012) Systematics of the hypervariable Moraea tripetala complex (Iridaceae: Iridoideae) of the southern African winter rainfall zone P. gOLDBLATT* and J.C. MAnnIng** Keywords: Chromosome cytology, Iridaceae, Iridoideae, Moraea Mill., new species, southern Africa, taxonomy ABSTRACT Field and laboratory research has shown that the Moraea tripetala complex of western South Africa, traditionally treated as a single species, sometimes with two additional varieties, has a pattern of morphological and cytological variation too complex to be accommodated in a single species. Variation in floral structure, especially the shape of the inner tepals, degree of union of the filaments, anther length and pollen colour form coherent patterns closely correlated with morphology of the corm tunics, mode of vegetative reproduction, and in some instances capsule and seed shape and size. The morphological patterns also correlate with geography, flowering time and sometimes habitat. It is especially significant that different vari- ants of the complex may co-occur, each with overlapping or separate flowering times, a situation that conflicts with a single species taxonomy. We propose recognizing nine species and three additional subspecies for plants currently assigned to M. tripetala. M. grandis, from the western Karoo, has virtually free filaments and leaves often ± plane distally; closely allied M. amabilis, also with ± free filaments and often hairy leaves, is centred in the western Karoo and Olifants River Valley. Its range overlaps that of M. cuspidata, which has narrowly channelled, smooth leaves, linear inner tepals spreading distally and filaments united for up to 1.5 mm.M. decipiens from the Piketberg, M. hainebachiana, a local endemic of coastal limestone fynbos in the Saldanha District, M. -
Moraea Insolens | Plantz Africa About:Reader?Url=
Moraea insolens | Plantz Africa about:reader?url=http://pza.sanbi.org/moraea-insolens pza.sanbi.org Moraea insolens | Plantz Africa Introduction Moraea insolens is a critically endangered, cormous plant, with dazzling orange-red or rarely white- or cream-coloured, salver-shaped blooms, with prominent, deep brown markings to attract its beetle pollinators. It is very rare in cultivation, but can be successfully grown as a container subject. Description Description This deciduous, winter-growing geophyte grows 200–350 mm high and has a small, rounded corm, protected by a covering of hard, light brown outer tunics. The corm produces two, dark brown, basal sheaths and has a solitary, linear, bright green, channelled leaf. The slender flower stem has prominent nodes and is sometimes branched, 1 of 7 2017/02/15 02:42 PM Moraea insolens | Plantz Africa about:reader?url=http://pza.sanbi.org/moraea-insolens producing a succession of salver-shaped flowers, each lasting three days, from between two spathe bracts. The tepals vary in shades of light to bright orange-red and are rarely white or cream-coloured. The three outer tepals are larger than the three inner ones and all are adorned with a deep brown, arrow-shaped marking near the base, sometimes outlined in white. The filaments are united into a central column with three long anthers symmetrically arranged opposite the three outer tepals. The anthers produce sticky, bright orange pollen. The fruit is an elliptic capsule containing many small, light brown, irregularly shaped seeds. The plant flowers from mid- to late spring (mid-September to mid-October) and is completely dormant in summer. -
Fruit Crops (To Distinguish Fruiting Varieties, Rootstocks, Ornamental Varieties), Roses, Lilies, Etc
Disclaimer: unless otherwise agreed by the Council of UPOV, only documents that have been adopted by the Council of UPOV and that have not been superseded can represent UPOV policies or guidance. This document has been scanned from a paper copy and may have some discrepancies from the original document. _____ Avertissement: sauf si le Conseil de l’UPOV en décide autrement, seuls les documents adoptés par le Conseil de l’UPOV n’ayant pas été remplacés peuvent représenter les principes ou les orientations de l’UPOV. Ce document a été numérisé à partir d’une copie papier et peut contenir des différences avec le document original. _____ Allgemeiner Haftungsausschluß: Sofern nicht anders vom Rat der UPOV vereinbart, geben nur Dokumente, die vom Rat der UPOV angenommen und nicht ersetzt wurden, Grundsätze oder eine Anleitung der UPOV wieder. Dieses Dokument wurde von einer Papierkopie gescannt und könnte Abweichungen vom Originaldokument aufweisen. _____ Descargo de responsabilidad: salvo que el Consejo de la UPOV decida de otro modo, solo se considerarán documentos de políticas u orientaciones de la UPOV los que hayan sido aprobados por el Consejo de la UPOV y no hayan sido reemplazados. Este documento ha sido escaneado a partir de una copia en papel y puede que existan divergencias en relación con el documento original. d:\users\renardy\appdata\local\microsoft\windows\temporary internet files\content.outlook\57qo7ps0\disclaimer_scanned_documents.docx 5 1 'E7 TC/35/10 ORIGINAL: English only DATE: March 2, 1999 INTERNATIONAL UNION FOR THE PROTECTION OF NEW VARIETIES OF PLANTS GENEVA TECHNICAL COMMITTEE Thirty-Fifth Session Geneva, March 22 to 24, 1999 WORKING PAPER FOR A UPOV TAXON CODE FOR USE IN THE UPOV-ROM PLANT VARIETY DATABASE Document prepared by the Office ofthe Union Introduction 1. -
Albania in Spring
Albania in Spring Naturetrek Tour Report 29 May - 5 June 2019 Dalmatian Pelican Elder-flowered Orchid Hermann Tortoise Spring Gentian Report and photos compiled by Neil Anderson Naturetrek Mingledown Barn Wolf's Lane Chawton Alton Hampshire GU34 3HJ UK T: +44 (0)1962 733051 E: [email protected] W: www.naturetrek.co.uk Tour Report Albania in Spring Tour participants: Neil Anderson (leader) & Mirjan Topi (local guide) with 16 Naturetrek clients Day 1 Wednesday 29th May Arrive Tirana We had a mid-afternoon flight departing Gatwick which left about 15 minutes late but arrived in Albania’s capital, Tirana, on time just before 21.00 local time. We were staying just a few minutes away at the comfortable Ark Hotel, where we checked in and were soon in our rooms settling down for a night’s sleep before the start of the tour. Day 2 Thursday 30th May Fllake-Sektori Rinia Lagoon, Karavasta, Berat We had a full programme after our breakfast in Tirana before heading for the scenic UNESCO city of Berat, our base for the next couple of days. We first visited the Rinia lagoon close to the capital and we were blessed with some pleasantly warm sunshine. This area is a popular beach location, but being a weekday there was little disturbance. Our first stop before the main lagoon was the unprotected site of a large Bee-eater breeding colony. Over 200 pairs breed here in total and we watched over 40 pairs. We also saw several Red-rumped Swallows here, had good views of a vocal Cuckoo and a Great Reed Warbler sang in the dyke. -
Nuclear and Plastid DNA Phylogeny of the Tribe Cardueae (Compositae
1 Nuclear and plastid DNA phylogeny of the tribe Cardueae 2 (Compositae) with Hyb-Seq data: A new subtribal classification and a 3 temporal framework for the origin of the tribe and the subtribes 4 5 Sonia Herrando-Morairaa,*, Juan Antonio Callejab, Mercè Galbany-Casalsb, Núria Garcia-Jacasa, Jian- 6 Quan Liuc, Javier López-Alvaradob, Jordi López-Pujola, Jennifer R. Mandeld, Noemí Montes-Morenoa, 7 Cristina Roquetb,e, Llorenç Sáezb, Alexander Sennikovf, Alfonso Susannaa, Roser Vilatersanaa 8 9 a Botanic Institute of Barcelona (IBB, CSIC-ICUB), Pg. del Migdia, s.n., 08038 Barcelona, Spain 10 b Systematics and Evolution of Vascular Plants (UAB) – Associated Unit to CSIC, Departament de 11 Biologia Animal, Biologia Vegetal i Ecologia, Facultat de Biociències, Universitat Autònoma de 12 Barcelona, ES-08193 Bellaterra, Spain 13 c Key Laboratory for Bio-Resources and Eco-Environment, College of Life Sciences, Sichuan University, 14 Chengdu, China 15 d Department of Biological Sciences, University of Memphis, Memphis, TN 38152, USA 16 e Univ. Grenoble Alpes, Univ. Savoie Mont Blanc, CNRS, LECA (Laboratoire d’Ecologie Alpine), FR- 17 38000 Grenoble, France 18 f Botanical Museum, Finnish Museum of Natural History, PO Box 7, FI-00014 University of Helsinki, 19 Finland; and Herbarium, Komarov Botanical Institute of Russian Academy of Sciences, Prof. Popov str. 20 2, 197376 St. Petersburg, Russia 21 22 *Corresponding author at: Botanic Institute of Barcelona (IBB, CSIC-ICUB), Pg. del Migdia, s. n., ES- 23 08038 Barcelona, Spain. E-mail address: [email protected] (S. Herrando-Moraira). 24 25 Abstract 26 Classification of the tribe Cardueae in natural subtribes has always been a challenge due to the lack of 27 support of some critical branches in previous phylogenies based on traditional Sanger markers.