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The Sphingidae (Lepidoptera) of the Philippines
©Entomologischer Verein Apollo e.V. Frankfurt am Main; download unter www.zobodat.at Nachr. entomol. Ver. Apollo, Suppl. 17: 17-132 (1998) 17 The Sphingidae (Lepidoptera) of the Philippines Willem H o g e n e s and Colin G. T r e a d a w a y Willem Hogenes, Zoologisch Museum Amsterdam, Afd. Entomologie, Plantage Middenlaan 64, NL-1018 DH Amsterdam, The Netherlands Colin G. T readaway, Entomologie II, Forschungsinstitut Senckenberg, Senckenberganlage 25, D-60325 Frankfurt am Main, Germany Abstract: This publication covers all Sphingidae known from the Philippines at this time in the form of an annotated checklist. (A concise checklist of the species can be found in Table 4, page 120.) Distribution maps are included as well as 18 colour plates covering all but one species. Where no specimens of a particular spe cies from the Philippines were available to us, illustrations are given of specimens from outside the Philippines. In total we have listed 117 species (with 5 additional subspecies where more than one subspecies of a species exists in the Philippines). Four tables are provided: 1) a breakdown of the number of species and endemic species/subspecies for each subfamily, tribe and genus of Philippine Sphingidae; 2) an evaluation of the number of species as well as endemic species/subspecies per island for the nine largest islands of the Philippines plus one small island group for comparison; 3) an evaluation of the Sphingidae endemicity for each of Vane-Wright’s (1990) faunal regions. From these tables it can be readily deduced that the highest species counts can be encountered on the islands of Palawan (73 species), Luzon (72), Mindanao, Leyte and Negros (62 each). -
The Ladybells Adenophora Liliifolia (L.) Besser in Forests Near Kisielany (Siedlce Upland, E Poland)
BRC Biodiv. Res. Conserv. 3-4: 324-328, 2006 www.brc.amu.edu.pl The ladybells Adenophora liliifolia (L.) Besser in forests near Kisielany (Siedlce Upland, E Poland) Marek T. Ciosek Department of Botany, Institute of Biology, University of Podlasie, B. Prusa 12, 08-110 Siedlce, Poland, e-mail: [email protected] Abstract: The ladybells Adenophora liliifolia in Poland was found in only 8 sites after 1980, so it is now classified as critically endangered (E). Since 2001 the species has been strictly protected and enlisted in the Habitat Directive of the EU. In 1995 in Kisielany, northwest of Siedlce, a rich population of Adenophora liliifolia was found. This study was undertaken to characterize phytosociologically the patches with ladybells and to analyse the structure of this population. One hundred specimens were randomly selected for population analysis carried out in 2005. Measurements were done on live plants. Seven individual traits were measured or calculated, including plant height, number of flowers, leaf dimensions, etc. The analysed patches represent thermophilous oak forest Potentillo albae-Qurcetum. This is the largest Polish population of this species known so far, as it consists of several hundred flowering specimens. Adenophora liliifolia achieves greatest dimensions there and its mean height exceeds the data known from the literature. Quantitative contribution of ladybells to particular patches varies from ì+î to ì2î according to the Braun-Blanquet scale. The plant is accompanied by some protected species, like: Laserpitium latifolium, Cimicifuga europaea, Aquilegia vulgaris and Lilium martagon. A proposal has been submitted to protect the site as a nature reserve and the population will be studied further. -
Plumeria Potpourri
Plumeria Potpourri www.thePlumeriasociety.org th President’s Corner Come to the July 11 meeting! by Mark Wright Tuesday, July 11, 2017, 7:30 p.m. page 2 Cherie Flores Garden Pavilion, 1500 Hermann Drive, Houston, Texas ... anyone with an interest in plumeria is invited to attend ... PSA Speaker Highlights—5/9/17 by David Holloway page 3 Jeannie Transformation page 3 Inducing Plumeria Dwarfism page 4 Observations on Some Plumeria in Cuba Stacy and Mike Atkinson by Donald R. Hodel page 5 A Plumeria Patchwork Mike Atkinson will share tidbits, insights, and wisdom Photos—PSA Seabrook/Clear Lake picked up from others and his own successes and Sale failures as a grower of nearly 20 years in Southern page 15 California. He’ll cover a hodgepodge of topics like photography, propagation, winter care, and more. He and New PSA his wife Stacy have over 200 plants in the ground (year Registrations round) and 300 in pots. They sell plants, cuttings, leis, page 20 arrangements, and have even done a plumeria wedding. The Plumeria Society of America, Inc. July 2017 President’s Corner by Mark Wright, Texas ([email protected]) The June plant sale is now behind us. It was a $35/year on January 1, 2018. The business card ad huge success, and everyone involved deserves a pat with membership will be $95/year, and the double on the back. This is the first sale I remember that size ad with membership will be $160/year. This will many, if not most, of the growers sold out. The July affect memberships which expire after January 1, sale is coming up soon, and we will need lots of 2018, leaving those expiring prior to that date at the volunteers to help it run smoothly too. -
Pteridologist 2007
PTERIDOLOGIST 2007 CONTENTS Volume 4 Part 6, 2007 EDITORIAL James Merryweather Instructions to authors NEWS & COMMENT Dr Trevor Walker Chris Page 166 A Chilli Fern? Graham Ackers 168 The Botanical Research Fund 168 Miscellany 169 IDENTIFICATION Male Ferns 2007 James Merryweather 172 TREE-FERN NEWSLETTER No. 13 Hyper-Enthusiastic Rooting of a Dicksonia Andrew Leonard 178 Most Northerly, Outdoor Tree Ferns Alastair C. Wardlaw 178 Dicksonia x lathamii A.R. Busby 179 Tree Ferns at Kells House Garden Martin Rickard 181 FOCUS ON FERNERIES Renovated Palace for Dicksoniaceae Alastair C. Wardlaw 184 The Oldest Fernery? Martin Rickard 185 Benmore Fernery James Merryweather 186 FEATURES Recording Ferns part 3 Chris Page 188 Fern Sticks Yvonne Golding 190 The Stansfield Memorial Medal A.R. Busby 191 Fern Collections in Manchester Museum Barbara Porter 193 What’s Dutch about Dutch Rush? Wim de Winter 195 The Fine Ferns of Flora Græca Graham Ackers 203 CONSERVATION A Case for Ex Situ Conservation? Alastair C. Wardlaw 197 IN THE GARDEN The ‘Acutilobum’ Saga Robert Sykes 199 BOOK REVIEWS Encyclopedia of Garden Ferns by Sue Olsen Graham Ackers 170 Fern Books Before 1900 by Hall & Rickard Clive Jermy 172 Britsh Ferns DVD by James Merryweather Graham Ackers 187 COVER PICTURE: The ancestor common to all British male ferns, the mountain male fern Dryopteris oreades, growing on a ledge high on the south wall of Bealach na Ba (the pass of the cattle) Unless stated otherwise, between Kishorn and Applecross in photographs were supplied the Scottish Highlands - page 172. by the authors of the articles PHOTO: JAMES MERRYWEATHER in which they appear. -
Accd Nuclear Transfer of Platycodon Grandiflorum and the Plastid of Early
Hong et al. BMC Genomics (2017) 18:607 DOI 10.1186/s12864-017-4014-x RESEARCH ARTICLE Open Access accD nuclear transfer of Platycodon grandiflorum and the plastid of early Campanulaceae Chang Pyo Hong1, Jihye Park2, Yi Lee3, Minjee Lee2, Sin Gi Park1, Yurry Uhm4, Jungho Lee2* and Chang-Kug Kim5* Abstract Background: Campanulaceae species are known to have highly rearranged plastid genomes lacking the acetyl-CoA carboxylase (ACC) subunit D gene (accD), and instead have a nuclear (nr)-accD. Plastid genome information has been thought to depend on studies concerning Trachelium caeruleum and genome announcements for Adenophora remotiflora, Campanula takesimana, and Hanabusaya asiatica. RNA editing information for plastid genes is currently unavailable for Campanulaceae. To understand plastid genome evolution in Campanulaceae, we have sequenced and characterized the chloroplast (cp) genome and nr-accD of Platycodon grandiflorum, a basal member of Campanulaceae. Results: We sequenced the 171,818 bp cp genome containing a 79,061 bp large single-copy (LSC) region, a 42,433 bp inverted repeat (IR) and a 7840 bp small single-copy (SSC) region, which represents the cp genome with the largest IR among species of Campanulaceae. The genome contains 110 genes and 18 introns, comprising 77 protein-coding genes, four RNA genes, 29 tRNA genes, 17 group II introns, and one group I intron. RNA editing of genes was detected in 18 sites of 14 protein-coding genes. Platycodon has an IR containing a 3′ rps12 operon, which occurs in the middle of the LSC region in four other species of Campanulaceae (T. caeruleum, A. remotiflora, C. -
(OUV) of the Wet Tropics of Queensland World Heritage Area
Handout 2 Natural Heritage Criteria and the Attributes of Outstanding Universal Value (OUV) of the Wet Tropics of Queensland World Heritage Area The notes that follow were derived by deconstructing the original 1988 nomination document to identify the specific themes and attributes which have been recognised as contributing to the Outstanding Universal Value of the Wet Tropics. The notes also provide brief statements of justification for the specific examples provided in the nomination documentation. Steve Goosem, December 2012 Natural Heritage Criteria: (1) Outstanding examples representing the major stages in the earth’s evolutionary history Values: refers to the surviving taxa that are representative of eight ‘stages’ in the evolutionary history of the earth. Relict species and lineages are the elements of this World Heritage value. Attribute of OUV (a) The Age of the Pteridophytes Significance One of the most significant evolutionary events on this planet was the adaptation in the Palaeozoic Era of plants to life on the land. The earliest known (plant) forms were from the Silurian Period more than 400 million years ago. These were spore-producing plants which reached their greatest development 100 million years later during the Carboniferous Period. This stage of the earth’s evolutionary history, involving the proliferation of club mosses (lycopods) and ferns is commonly described as the Age of the Pteridophytes. The range of primitive relict genera representative of the major and most ancient evolutionary groups of pteridophytes occurring in the Wet Tropics is equalled only in the more extensive New Guinea rainforests that were once continuous with those of the listed area. -
Flora Mediterranea 26
FLORA MEDITERRANEA 26 Published under the auspices of OPTIMA by the Herbarium Mediterraneum Panormitanum Palermo – 2016 FLORA MEDITERRANEA Edited on behalf of the International Foundation pro Herbario Mediterraneo by Francesco M. Raimondo, Werner Greuter & Gianniantonio Domina Editorial board G. Domina (Palermo), F. Garbari (Pisa), W. Greuter (Berlin), S. L. Jury (Reading), G. Kamari (Patras), P. Mazzola (Palermo), S. Pignatti (Roma), F. M. Raimondo (Palermo), C. Salmeri (Palermo), B. Valdés (Sevilla), G. Venturella (Palermo). Advisory Committee P. V. Arrigoni (Firenze) P. Küpfer (Neuchatel) H. M. Burdet (Genève) J. Mathez (Montpellier) A. Carapezza (Palermo) G. Moggi (Firenze) C. D. K. Cook (Zurich) E. Nardi (Firenze) R. Courtecuisse (Lille) P. L. Nimis (Trieste) V. Demoulin (Liège) D. Phitos (Patras) F. Ehrendorfer (Wien) L. Poldini (Trieste) M. Erben (Munchen) R. M. Ros Espín (Murcia) G. Giaccone (Catania) A. Strid (Copenhagen) V. H. Heywood (Reading) B. Zimmer (Berlin) Editorial Office Editorial assistance: A. M. Mannino Editorial secretariat: V. Spadaro & P. Campisi Layout & Tecnical editing: E. Di Gristina & F. La Sorte Design: V. Magro & L. C. Raimondo Redazione di "Flora Mediterranea" Herbarium Mediterraneum Panormitanum, Università di Palermo Via Lincoln, 2 I-90133 Palermo, Italy [email protected] Printed by Luxograph s.r.l., Piazza Bartolomeo da Messina, 2/E - Palermo Registration at Tribunale di Palermo, no. 27 of 12 July 1991 ISSN: 1120-4052 printed, 2240-4538 online DOI: 10.7320/FlMedit26.001 Copyright © by International Foundation pro Herbario Mediterraneo, Palermo Contents V. Hugonnot & L. Chavoutier: A modern record of one of the rarest European mosses, Ptychomitrium incurvum (Ptychomitriaceae), in Eastern Pyrenees, France . 5 P. Chène, M. -
Adenophora Liliifolia: Condition of Its Populations in Central Europe
ACTA BIOLOGICA CRACOVIENSIA Series Botanica 58/2: 83–105, 2016 DOI: 10.1515/abcsb-2016-0018 ADENOPHORA LILIIFOLIA: CONDITION OF ITS POPULATIONS IN CENTRAL EUROPE ROMANA PRAUSOVÁ1a*, LUCIE MAREČKOVÁ2a, ADAM KAPLER3, L’UBOŠ MAJESKÝ2, TÜNDE FARKAS4, ADRIAN INDREICA5, LENKA ŠAFÁŘOVÁ6 AND MILOSLAV KITNER2 1University of Hradec Králové, Faculty of Science, Department of Biology, 500 02 Hradec Králové, Czech Republic 2Palacký University in Olomouc, Faculty of Science, Department of Botany, Šlechtitelů 27, 783 71 Olomouc-Holice, Czech Republic 3PAS Botanical Garden – Center for Biological Diversity Conservation in Powsin, Prawdziwka 2, 02-973 Warsaw 76, Poland 4Aggteleki Nemzeti Park Igazgatóság, Tengerszem oldal 1, 3759 Jósvafő, Hungary 5Transilvania University of Brasov, Faculty of Forestry, Şirul Beethoven – 1, 500123 Braşov, Romania 6East Bohemian Museum in Pardubice, Zámek 2, 530 02 Pardubice, Czech Republic Received June 16, 2016; revision accepted September 30, 2016 This study deals with populations of the European-South-Siberian geoelement Adenophora liliifolia (L.) A. DC. in the Czech Republic, Slovakia, Hungary, Romania, and Poland, where this species has its European periphery distri- bution. We studied the population size, genetic variability, site conditions, and vegetation units in which A. liliifolia grows.Keywords: Recent and historical localities of A. liliifolia were ranked into six vegetation units of both forest and non-for- est character. A phytosociological survey showed differences in the species composition among localities. Only a weak pattern of population structure was observed (only 22% of total genetic variation present at the interpopulation level, AMOVA analysis), with moderate values for gene diversity (Hj = 0.141) and polymorphism (P = 27.6%). Neighbor- joining and Bayesian clusterings suggest a similar genetic background for most of the populations from Slovakia, the Czech Republic, and Poland, contrary to the populations from Hungary, Romania, as well as two populations from Central and South Slovakia. -
Fern Classification
16 Fern classification ALAN R. SMITH, KATHLEEN M. PRYER, ERIC SCHUETTPELZ, PETRA KORALL, HARALD SCHNEIDER, AND PAUL G. WOLF 16.1 Introduction and historical summary / Over the past 70 years, many fern classifications, nearly all based on morphology, most explicitly or implicitly phylogenetic, have been proposed. The most complete and commonly used classifications, some intended primar• ily as herbarium (filing) schemes, are summarized in Table 16.1, and include: Christensen (1938), Copeland (1947), Holttum (1947, 1949), Nayar (1970), Bierhorst (1971), Crabbe et al. (1975), Pichi Sermolli (1977), Ching (1978), Tryon and Tryon (1982), Kramer (in Kubitzki, 1990), Hennipman (1996), and Stevenson and Loconte (1996). Other classifications or trees implying relationships, some with a regional focus, include Bower (1926), Ching (1940), Dickason (1946), Wagner (1969), Tagawa and Iwatsuki (1972), Holttum (1973), and Mickel (1974). Tryon (1952) and Pichi Sermolli (1973) reviewed and reproduced many of these and still earlier classifica• tions, and Pichi Sermolli (1970, 1981, 1982, 1986) also summarized information on family names of ferns. Smith (1996) provided a summary and discussion of recent classifications. With the advent of cladistic methods and molecular sequencing techniques, there has been an increased interest in classifications reflecting evolutionary relationships. Phylogenetic studies robustly support a basal dichotomy within vascular plants, separating the lycophytes (less than 1 % of extant vascular plants) from the euphyllophytes (Figure 16.l; Raubeson and Jansen, 1992, Kenrick and Crane, 1997; Pryer et al., 2001a, 2004a, 2004b; Qiu et al., 2006). Living euphyl• lophytes, in turn, comprise two major clades: spermatophytes (seed plants), which are in excess of 260 000 species (Thorne, 2002; Scotland and Wortley, Biology and Evolution of Ferns and Lycopliytes, ed. -
The Paraphyly of Osmunda Is Confirmed by Phylogenetic Analyses of Seven Plastid Loci
Systematic Botany (2008), 33(1): pp. 31–36 © Copyright 2008 by the American Society of Plant Taxonomists The Paraphyly of Osmunda is Confirmed by Phylogenetic Analyses of Seven Plastid Loci Jordan S. Metzgar,1 Judith E. Skog,2,3 Elizabeth A. Zimmer,4 and Kathleen M. Pryer1,5 1Department of Biology, Duke University, Durham, North Carolina 27708 U.S.A. 2Department of Environmental Science and Policy, George Mason University, Fairfax, Virginia 22030 U.S.A. 3National Science Foundation, Division of Biological Infrastructure, 4201 Wilson Blvd., Arlington, Virginia 22203 U.S.A. 4Department of Botany and Laboratory of Analytical Biology, Smithsonian Museum Support Center, 4210 Silver Hill Road, Suitland, Maryland 20746 U.S.A. 5Author for correspondence ([email protected]) Communicating Editor: Daniel Potter Abstract—To resolve phylogenetic relationships among all genera and subgenera in Osmundaceae, we analyzed over 8,500 characters of DNA sequence data from seven plastid loci (atpA, rbcL, rbcL–accD, rbcL–atpB, rps4–trnS, trnG–trnR, and trnL–trnF). Our results confirm those from earlier anatomical and single-gene (rbcL) studies that suggested Osmunda s.l. is paraphyletic. Osmunda cinnamomea is sister to the remainder of Osmundaceae (Leptopteris, Todea, and Osmunda s.s.). We support the recognition of a monotypic fourth genus, Osmundastrum, to reflect these results. We also resolve subgeneric relationships within Osmunda s.s. and find that subg. Claytosmunda is strongly supported as sister to the rest of Osmunda. A stable, well-supported classification for extant Osmundaceae is proposed, along with a key to all genera and subgenera. Keywords—ferns, Osmunda, Osmundaceae, Osmundastrum, paraphyly, plastid DNA. -
Panama: Fall at El Valle's Canopy Lodge
PANAMA: FALL AT EL VALLE’S CANOPY LODGE SEPTEMBER 29–OCTOBER 6, 2018 Spectacled Owl, El Valle, Panama, October 1, 2018, Barry Zimmer LEADERS: BARRY ZIMMER, VICTOR EMANUEL, & CARLOS BETHANCOURT LIST COMPILED BY: BARRY ZIMMER VICTOR EMANUEL NATURE TOURS, INC. 2525 WALLINGWOOD DRIVE, SUITE 1003 AUSTIN, TEXAS 78746 WWW.VENTBIRD.COM PANAMA: FALL AT EL VALLE’S CANOPY LODGE SEPTEMBER 29–OCTOBER 6, 2018 By Barry Zimmer There were so many magical moments on our weeklong Canopy Lodge tour that it is hard to know where to start in describing the highlights of our awesome trip. Perhaps, the twenty minutes spent marveling at a family group of Spectacled Owls no more than 60 feet away should top the list. The pair, with their fledged young bird at their side, allowed lengthy studies and superb photographic opportunities. These owls were voted the runaway winner of the “favorite bird of the tour” competition. And yet, was it even the most memorable bird sighting of the day? On that same day, we tallied a rare “motmot slam”—four species of motmots in the same day. From the impressive Rufous Motmot dominating the Lodge feeders at dawn to the wonderful pair of Broad-billed Motmots that posed along the Las Minas Road right over our heads, to the furtive Tody Motmot that eventually allowed great scope views, and to the Lesson’s Motmot late in the day with its electric-blue crown glowing in the afternoon sun, we enjoyed incredible views of all four species. In how many locales can one tally four species of motmots in a day? And what about the thirty minutes spent watching a fruiting Ficus tree along the Las Minas Road earlier that same day? It seemed like every color in the rainbow was represented by the birds visiting the tree that morning. -
Greater Antilles
Greater Antilles Jamaica, Cuba, Dominican Republic, and Puerto Rico (and Cayman Islands) Todies and Tyrants A Greentours Tour Report th th 27 November to 18 December 2014 Led by Paul Cardy Trip report written by Paul Cardy Introduction This ambitious tour of all the main Greater Antillean islands gives the chance to see a wealth of single island and regional endemic birds, butterflies and reptiles. Some 110 endemic birds were recorded, including all five of the world’s todys, endemic to the region. Our trip took us through five remarkably contrasting countries and cultures. Beautiful scenery, from the misty Blue Mountains of Jamaica, to the swamps of Cuba’s Zapata peninsula, Dominican Republic’s forested mountains, and the Guanica Dry Forest in Puerto Rico characterised the journey. A remarkably varied tour, illustrated by the Cuban example of watching Blue-headed Quail-Doves on forest trails in Zapata, and also experiencing the vibrancy of fascinating Old Havana. A feature was the incredible views we had of many rare endemic birds, such as Chestnut-bellied Cuckoo and both endemic parrots on Jamaica; Bee Hummingbird, Fernadina’s Flicker, and Zapata Wren on Cuba; Hispaniolan Woodpecker and Black-crowned Palm-Tanager in Dominican Republic; and Elfin Woods Warbler on Puerto Rico. There were some very special butterflies too such as Grand Cayman Swallowtail, Jamaican Monarch, two species of Anetia, Haitian Snout, Haitian Admiral, Cuban Emperor, Dusky Emperor, Cuban Lucinia, Cuban Dagger Tail, seven species of Calisto, and Haitian Pygmy Skipper. One area in Hispaniola, discovered on the previous visit, proved especially good for butterflies.