Orchids and Evolution by Natural Selection
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Charles Darwin: a Companion
CHARLES DARWIN: A COMPANION Charles Darwin aged 59. Reproduction of a photograph by Julia Margaret Cameron, original 13 x 10 inches, taken at Dumbola Lodge, Freshwater, Isle of Wight in July 1869. The original print is signed and authenticated by Mrs Cameron and also signed by Darwin. It bears Colnaghi's blind embossed registration. [page 3] CHARLES DARWIN A Companion by R. B. FREEMAN Department of Zoology University College London DAWSON [page 4] First published in 1978 © R. B. Freeman 1978 All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted, in any form or by any means, electronic, mechanical, photocopying, recording or otherwise without the permission of the publisher: Wm Dawson & Sons Ltd, Cannon House Folkestone, Kent, England Archon Books, The Shoe String Press, Inc 995 Sherman Avenue, Hamden, Connecticut 06514 USA British Library Cataloguing in Publication Data Freeman, Richard Broke. Charles Darwin. 1. Darwin, Charles – Dictionaries, indexes, etc. 575′. 0092′4 QH31. D2 ISBN 0–7129–0901–X Archon ISBN 0–208–01739–9 LC 78–40928 Filmset in 11/12 pt Bembo Printed and bound in Great Britain by W & J Mackay Limited, Chatham [page 5] CONTENTS List of Illustrations 6 Introduction 7 Acknowledgements 10 Abbreviations 11 Text 17–309 [page 6] LIST OF ILLUSTRATIONS Charles Darwin aged 59 Frontispiece From a photograph by Julia Margaret Cameron Skeleton Pedigree of Charles Robert Darwin 66 Pedigree to show Charles Robert Darwin's Relationship to his Wife Emma 67 Wedgwood Pedigree of Robert Darwin's Children and Grandchildren 68 Arms and Crest of Robert Waring Darwin 69 Research Notes on Insectivorous Plants 1860 90 Charles Darwin's Full Signature 91 [page 7] INTRODUCTION THIS Companion is about Charles Darwin the man: it is not about evolution by natural selection, nor is it about any other of his theoretical or experimental work. -
Hawk Moths of North America Is Richly Illustrated with Larval Images and Contains an Abundance of Life History Information
08 caterpillars EUSA/pp244-273 3/9/05 6:37 PM Page 244 244 TULIP-TREE MOTH CECROPIA MOTH 245 Callosamia angulifera Hyalophora cecropia RECOGNITION Frosted green with shiny yellow, orange, and blue knobs over top and sides of body. RECOGNITION Much like preceding but paler or Dorsal knobs on T2, T3, and A1 somewhat globular and waxier in color with pale stripe running below set with black spinules. Paired knobs on A2–A7 more spiracles on A1–A10 and black dots on abdomen cylindrical, yellow; knob over A8 unpaired and rounded. lacking contrasting pale rings. Yellow abdominal Larva to 10cm. Caterpillars of larch-feeding Columbia tubercle over A8 short, less than twice as high as broad. Silkmoth (Hyalophora columbia) have yellow-white to Larva to 6cm. Sweetbay Silkmoth (Callosamia securifera) yellow-pink instead of bright yellow knobs over dorsum similar in appearance but a specialist on sweet bay. Its of abdomen and knobs along sides tend to be more white than blue (as in Cecropia) and are yellow abdominal tubercle over A8 is nearly three times as set in black bases (see page 246). long as wide and the red knobs over thorax are cylindrical (see page 246). OCCURRENCE Urban and suburban yards and lots, orchards, fencerows, woodlands, OCCURRENCE Woodlands and forests from Michigan, southern Ontario, and and forests from Canada south to Florida and central Texas. One generation with mature Massachusetts to northern Florida and Mississippi. One principal generation northward; caterpillars from late June through August over most of range. two broods in South with mature caterpillars from early June onward. -
On European Honeybee (Apis Mellifera L.) Apiary at Mid-Hill Areas of Lalitpur District, Nepal Sanjaya Bista1,2*, Resham B
Journal of Agriculture and Natural Resources (2020) 3(1): 117-132 ISSN: 2661-6270 (Print), ISSN: 2661-6289 (Online) DOI: https://doi.org/10.3126/janr.v3i1.27105 Research Article Incidence and predation rate of hornet (Vespa spp.) on European honeybee (Apis mellifera L.) apiary at mid-hill areas of Lalitpur district, Nepal Sanjaya Bista1,2*, Resham B. Thapa2, Gopal Bahadur K.C.2, Shree Baba Pradhan1, Yuga Nath Ghimire3 and Sunil Aryal1 1Nepal Agricultural Research Council, Entomology Division, Khumaltar, Lalitpur, Nepal 2Institute of Agriculture and Animal Science, Tribhuvan University, Kirtipur, Kathmandu, Nepal 3Socio-Economics and Agricultural Research Policy Division (SARPOD), NARC, Khumaltar, Nepal * Correspondence: [email protected] ORCID: https://orcid.org/0000-0002-5219-3399 Received: July 08, 2019; Accepted: September 28, 2019; Published: January 7, 2020 © Copyright: Bista et al. (2020). This work is licensed under a Creative Commons Attribution-Non Commercial 4.0 International License. ABSTRACT Predatory hornets are considered as one of the major constraints to beekeeping industry. Therefore, its incidence and predation rate was studied throughout the year at two locations rural and forest areas of mid-hill in Laliptur district during 2016/017 to 2017/018. Observation was made on the number of hornet and honeybee captured by hornet in three different times of the day for three continuous minutes every fortnightly on five honeybee colonies. During the study period, major hornet species captured around the honeybee apiary at both locations were, Vespa velutina Lepeletier, Vespa basalis Smith, Vespa tropica (Linnaeus) and Vespa mandarina Smith. The hornet incidence varied significantly between the years and locations along with different observation dates. -
Phylogeny and Biogeography of Hawkmoths (Lepidoptera: Sphingidae): Evidence from Five Nuclear Genes
Phylogeny and Biogeography of Hawkmoths (Lepidoptera: Sphingidae): Evidence from Five Nuclear Genes Akito Y. Kawahara1*, Andre A. Mignault1, Jerome C. Regier2, Ian J. Kitching3, Charles Mitter1 1 Department of Entomology, College Park, Maryland, United States of America, 2 Center for Biosystems Research, University of Maryland Biotechnology Institute, College Park, Maryland, United States of America, 3 Department of Entomology, The Natural History Museum, London, United Kingdom Abstract Background: The 1400 species of hawkmoths (Lepidoptera: Sphingidae) comprise one of most conspicuous and well- studied groups of insects, and provide model systems for diverse biological disciplines. However, a robust phylogenetic framework for the family is currently lacking. Morphology is unable to confidently determine relationships among most groups. As a major step toward understanding relationships of this model group, we have undertaken the first large-scale molecular phylogenetic analysis of hawkmoths representing all subfamilies, tribes and subtribes. Methodology/Principal Findings: The data set consisted of 131 sphingid species and 6793 bp of sequence from five protein-coding nuclear genes. Maximum likelihood and parsimony analyses provided strong support for more than two- thirds of all nodes, including strong signal for or against nearly all of the fifteen current subfamily, tribal and sub-tribal groupings. Monophyly was strongly supported for some of these, including Macroglossinae, Sphinginae, Acherontiini, Ambulycini, Philampelini, Choerocampina, and Hemarina. Other groupings proved para- or polyphyletic, and will need significant redefinition; these include Smerinthinae, Smerinthini, Sphingini, Sphingulini, Dilophonotini, Dilophonotina, Macroglossini, and Macroglossina. The basal divergence, strongly supported, is between Macroglossinae and Smerinthinae+Sphinginae. All genes contribute significantly to the signal from the combined data set, and there is little conflict between genes. -
“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. -
Archiv Für Naturgeschichte
© Biodiversity Heritage Library, http://www.biodiversitylibrary.org/; www.zobodat.at Lepidoptera für 1903. Bearbeitet von Dr. Robert Lucas in Rixdorf bei Berlin. A. Publikationen (Autoren alphabetisch) mit Referaten. Adkin, Robert. Pyrameis cardui, Plusia gamma and Nemophila noc- tuella. The Entomologist, vol. 36. p. 274—276. Agassiz, G. Etüde sur la coloration des ailes des papillons. Lausanne, H. Vallotton u. Toso. 8 °. 31 p. von Aigner-Abafi, A. (1). Variabilität zweier Lepidopterenarten. Verhandlgn. zool.-bot. Ges. Wien, 53. Bd. p. 162—165. I. Argynnis Paphia L. ; IL Larentia bilineata L. — (2). Protoparce convolvuli. Entom. Zeitschr. Guben. 17. Jahrg. p. 22. — (3). Über Mimikry. Gaea. 39. Jhg. p. 166—170, 233—237. — (4). A mimicryröl. Rov. Lapok, vol. X, p. 28—34, 45—53 — (5). A Mimicry. Allat. Kozl. 1902, p. 117—126. — (6). (Über Mimikry). Allgem. Zeitschr. f. Entom. 7. Bd. (Schluß p. 405—409). Über Falterarten, welche auch gesondert von ihrer Umgebung, in ruhendem Zustande eine eigentümliche, das Auge täuschende Form annehmen (Lasiocampa quercifolia [dürres Blatt], Phalera bucephala [zerbrochenes Ästchen], Calocampa exoleta [Stück morschen Holzes]. — [Stabheuschrecke, Acanthoderus]. Raupen, die Meister der Mimikry sind. Nachahmung anderer Tiere. Die Mimik ist in vielen Fällen zwecklos. — Die wenn auch recht geistreichen Mimikry-Theorien sind doch vielleicht nur ein müßiges Spiel der Phantasie. Aitken u. Comber, E. A list of the butterflies of the Konkau. Journ. Bombay Soc. vol. XV. p. 42—55, Suppl. p. 356. Albisson, J. Notes biologiques pour servir ä l'histoire naturelle du Charaxes jasius. Bull. Soc. Etud. Sc. nat. Nimes. T. 30. p. 77—82. Annandale u. Robinson. Siehe unter S w i n h o e. -
Otter Slough Conservation Area (Stoddard County, Missouri) by Hugo L
SOUTHERN LEPIDOPTERISTS’ NEWS VOLUME 43 NO. 2 (2021), PG. 159 A LEPIDOPTERA BIODIVERSITY BLITZ AT THE OTTER SLOUGH CONSERVATION AREA (STODDARD COUNTY, MISSOURI) BY HUGO L. KONS JR. 1 & ROBERT J. BORTH 2 ABSTRACT We conducted a Lepidoptera biodiversity blitz on 3 and Catocala crataegi complex, representing the most 4 June 2018 at the Otter Slough Conservation Area in northerly locality that we are aware of for these Stoddard County, Missouri. We documented as many phenotypes. Recent material was needed for DNA Lepidoptera species as possible with MV/UV lights, sequencing. rotten banana/brown sugar bait, and diurnal collecting with nets. We present records for 235 species, including From 3-4 June 2018 we visited the Otter Slough 193 Macrolepidoptera and 19 Rhopalocera 3. Habitats Conservation Area to sample Catocala and document as sampled include hydric hardwood forest, cypress many other co-occurring Lepidoptera species as swamp, open wetlands, and field. Examples of some possible. This paper reports the Macrolepidoptera and species are shown on 15 color plates of live photos and Rhopalocera species recorded during this survey. This pinned specimens research was conducted under Wildlife Collectors Permit #17910 issued by the Missouri Department of INTRODUCTION Conservation. The Otter Slough Conservation Area is a 4,866 acre area MATERIALS AND METHODS including hydric hardwood forest (Figure 2:B, E-H), cypress-tupelo swamp (Figure 2:A), open marsh with Lepidoptera were sampled with a 400 watt MV cattails, sedge meadow, and cypress (Figure 2:D), illuminated sheet, 175 watt MV light trap, 15 watt UV mowed field (Figure 2:C (middle)), and slough habitats. -
Occurrence and Molecular Phylogeny of Honey Bee Viruses in Vespids
viruses Article Occurrence and Molecular Phylogeny of Honey Bee Viruses in Vespids 1,2, 3, 4, 5, 5, Sa Yang y, Philippe Gayral y, Hongxia Zhao y, Yaojun Wu y, Xuejian Jiang y, 1,2 3, 1,2 1,2 3 Yanyan Wu , Diane Bigot z, Xinling Wang , Dahe Yang , Elisabeth A. Herniou , 1,2 1,2 1,2 3, , 1,2, , Shuai Deng , Fei Li , Qingyun Diao , Eric Darrouzet * y and Chunsheng Hou * y 1 Institute of Apicultural Research, Chinese Academy of Agricultural Sciences, Beijing 100093, China; [email protected] (S.Y.); [email protected] (Y.W.); [email protected] (X.W.); [email protected] (D.Y.); [email protected] (S.D.); [email protected] (F.L.); [email protected] (Q.D.) 2 Key Laboratory of Pollinating Insect Biology, Ministry of Agriculture, Beijing 100093, China 3 Institut de Recherche sur la Biologie de l’Insecte, UMR 7261, CNRS—Université de Tours, F-37200 Tours, France; [email protected] (P.G.); [email protected] (D.B.); [email protected] (E.A.H.) 4 Guangdong Key Laboratory of Animal Conservation and Resource Utilization, Guangdong Public Laboratory of Wild Animal Conservation and Utilization, Guangdong Institute of Applied Biological Resources, Guangzhou 510260, China; [email protected] 5 Institute of Forestry Protection, Guangxi Zhuang Autonomous Region Forestry Research Institute, Nanning 530002, China; [email protected] (Y.W.); [email protected] (X.J.) * Correspondence: [email protected] (E.D.); [email protected] (C.H.); Tel.: +33-(0)2-47-36-71-60 (E.D.); +86-1062597285 (C.H.) These authors contributed equally to this work. -
A History of Orchids. a History of Discovery, Lust and Wealth
Scientific Papers. Series B, Horticulture. Vol. LXIV, No. 1, 2020 Print ISSN 2285-5653, CD-ROM ISSN 2285-5661, Online ISSN 2286-1580, ISSN-L 2285-5653 A HISTORY OF ORCHIDS. A HISTORY OF DISCOVERY, LUST AND WEALTH Nora Eugenia D. G. ANGHELESCU1, Annie BYGRAVE2, Mihaela I. GEORGESCU1, Sorina A. PETRA1, Florin TOMA1 1University of Agronomic Sciences and Veterinary Medicine of Bucharest, 59 Mărăști Blvd, District 1, Bucharest, Romania 2Self-employed, London, UK Corresponding author email: [email protected] Abstract Orchidaceae is the second largest families of flowering plants. There are approximately 900 orchid genera comprising between 28,000-32,000 species of orchids. The relationship between orchids and mankind is complex. The history of orchids’ discovery goes hand in hand with the history of humanity, encompassing discovery and adventure, witchcraft and magic, symbolism and occultism, addiction and sacrifice, lust and wealth. Historically, the Chinese were the first to cultivate orchids as medicinal plants, more than 4000 years ago. Gradually, records about orchids spread, reaching the Middle East and Europe. Around 300 B.C., Theophrastus named them for the first time orkhis. In 1737, Carl Linnaeus first used the word Orchidaceae to designate plants with similar features. The family name, Orchidaceae was fully established in 1789, by Antoine Laurent de Jussieu. In 1862, Charles Darwin published the first edition of his book, Fertilisation of Orchids. Darwin considered the adaptations of orchid flowers to their animal pollinators as being among the best examples of his idea of evolution through natural selection. Orchidology was on its way. During the 18th and the 19th centuries, orchids generated the notorious Orchid Fever where orchid-hunters turned the search for orchids into a frantic and obsessive hunt. -
Analysis of the Secondary Nest of the Yellow-Legged Hornet Found in the Balearic Islands Reveals Its High Adaptability to Mediterranean Isolated Ecosystems
C. Herrera, A. Marqués, V. Colomar and M.M. Leza Herrera, C.; A. Marqués, V. Colomar and M.M. Leza. Analysis of the secondary nest of the yellow-legged hornet found in the Balearic Islands reveals its high adaptability to Mediterranean isolated ecosystems Analysis of the secondary nest of the yellow-legged hornet found in the Balearic Islands reveals its high adaptability to Mediterranean isolated ecosystems C. Herrera1, A. Marqués1, V. Colomar2 and M.M. Leza1 1Laboratory of Zoology, Department of Biology, University of the Balearic Islands, Cra. Valldemossa km 7.5, CP: 07122 Palma, Illes Balears, Spain. <[email protected]>. 2Consortium for the Recovery of the Fauna of the Balearic Islands (COFIB), Crta. Sineu km 15, CP: 07142 Santa Eugènia, Illes Balears, Spain. Abstract The yellow-legged hornet (Vespa velutina) was detected for the fi rst time in the north of Spain in 2010, but was not detected in Majorca, Balearic Islands until 2015 and only one secondary nest, with 10 combs, was found in the northwest of the island. During 2016, nine more nests were found in the same region. To better understand the biology of V. velutina in isolated conditions, the following objectives were proposed: (I) describe the architecture and structure of nests; (II) analyse the shape of combs and develop a new method to confi rm the circular pattern of breeding; (III) determine the colony size and (IV) determine the succession of workers and sexual individuals throughout the season. For these reasons, nests that were removed were frozen for at least 48 days until analysis. -
A FURTHER FIELD NOTE on ISOPARCE CUPRESSI (SPHINGIDAE) a Description of the Larva of Isoparce Cupressi (Bdv.) Was Given by the Author (1973, J
VOLUME 28, NUMBER 2 157 dominal prolegs light grayish-brown. Anal shield and lateral sclerites on anal prolegs dark grayish-brown. Fourth and Fifth Instar (Fig. 2 D). Head yellowish-brown suffused with light brown markings. Frons and adfrontals paler. Ocellar area black. Body creamy white with maroon transverse band on anterior half of meso- and meta thorax and abdominal segments 1-9. Bands on mesothorax and 9th abdominal segment noticeably paler. Prothoracic shield whitish with 6 irregular black spots. Thoracic legs pale basally gradually darkening to grayish-brown on tarsus. Anal shield pale yellowish-brown. Spiracles dark brown with black peritreme. Pre spiracular sclerite black, pinacula brown. Pupa (Fig. 2 A, B, C). Lightly sclerotized, light orangish-brown. Spiracles in shallow depression, rims of spiracles projecting above cuticular surface. Anterior margins of abdominal segments 5, 6, and 7 strongly pitted. Proboscis length variable, exposing metathoracic legs as figured or extending completely to apex of wings. Cremaster consisting of 2 elongate spines curving slightly ventrad. ACKNOWLEDGMENTS The assistance of Mrs. Sandra Shuler in various phases of this study and of Mrs. Phyllis Habeck for the illustrations is gratefully acknowl edged. Identification of the wasp was by Dr. Eric Grissell and the spider by Dr. Karl Stone. LITERATURE CITED FORBES, W. T. M. 1954. Lepidoptera of New York and Neighboring States. Part 3. Cornell Univ. Agr. Exp. Sta. Mem. 329. 433 p. GANYARD, M. C. & U. E. BRADY. 1972. Interspecific attraction in Lepidoptera in the field. Ann. Entomo!. Soc. Amer. 65: 1279-1282. HARDWICK, D. F. 1958. Taxonomy, life history, and habits of the elliptoid-eyed species of Schinia (Lepidoptera: Noctuidae), with notes on the Heliothidinae. -
Insect Venom Phospholipases A1 and A2 Roles in the Envenoming Process and Allergy
Insect Biochemistry and Molecular Biology 105 (2019) 10–24 Contents lists available at ScienceDirect Insect Biochemistry and Molecular Biology journal homepage: www.elsevier.com/locate/ibmb Insect venom phospholipases A1 and A2: Roles in the envenoming process and allergy T Amilcar Perez-Riverola, Alexis Musacchio Lasab, José Roberto Aparecido dos Santos-Pintoa, ∗ Mario Sergio Palmaa, a Center of the Study of Social Insects, Department of Biology, Institute of Biosciences of Rio Claro, São Paulo State University (UNESP), Rio Claro, SP, 13500, Brazil b Center for Genetic Engineering and Biotechnology, Biomedical Research Division, Department of System Biology, Ave. 31, e/158 and 190, P.O. Box 6162, Cubanacan, Playa, Havana, 10600, Cuba ARTICLE INFO ABSTRACT Keywords: Insect venom phospholipases have been identified in nearly all clinically relevant social Hymenoptera, including Hymenoptera bees, wasps and ants. Among other biological roles, during the envenoming process these enzymes cause the Venom phospholipases A1 and A2 disruption of cellular membranes and induce hypersensitive reactions, including life threatening anaphylaxis. ff Toxic e ects While phospholipase A2 (PLA2) is a predominant component of bee venoms, phospholipase A1 (PLA1) is highly Hypersensitive reactions abundant in wasps and ants. The pronounced prevalence of IgE-mediated reactivity to these allergens in sen- Allergy diagnosis sitized patients emphasizes their important role as major elicitors of Hymenoptera venom allergy (HVA). PLA1 and -A2 represent valuable marker allergens for differentiation of genuine sensitizations to bee and/or wasp venoms from cross-reactivity. Moreover, in massive attacks, insect venom phospholipases often cause several pathologies that can lead to fatalities. This review summarizes the available data related to structure, model of enzymatic activity and pathophysiological roles during envenoming process of insect venom phospholipases A1 and -A2.