Globally Important Agricultural Heritage Systems (GIAHS) Application
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
The Mitochondrial Genomes of Palaeopteran Insects and Insights
www.nature.com/scientificreports OPEN The mitochondrial genomes of palaeopteran insects and insights into the early insect relationships Nan Song1*, Xinxin Li1, Xinming Yin1, Xinghao Li1, Jian Yin2 & Pengliang Pan2 Phylogenetic relationships of basal insects remain a matter of discussion. In particular, the relationships among Ephemeroptera, Odonata and Neoptera are the focus of debate. In this study, we used a next-generation sequencing approach to reconstruct new mitochondrial genomes (mitogenomes) from 18 species of basal insects, including six representatives of Ephemeroptera and 11 of Odonata, plus one species belonging to Zygentoma. We then compared the structures of the newly sequenced mitogenomes. A tRNA gene cluster of IMQM was found in three ephemeropteran species, which may serve as a potential synapomorphy for the family Heptageniidae. Combined with published insect mitogenome sequences, we constructed a data matrix with all 37 mitochondrial genes of 85 taxa, which had a sampling concentrating on the palaeopteran lineages. Phylogenetic analyses were performed based on various data coding schemes, using maximum likelihood and Bayesian inferences under diferent models of sequence evolution. Our results generally recovered Zygentoma as a monophyletic group, which formed a sister group to Pterygota. This confrmed the relatively primitive position of Zygentoma to Ephemeroptera, Odonata and Neoptera. Analyses using site-heterogeneous CAT-GTR model strongly supported the Palaeoptera clade, with the monophyletic Ephemeroptera being sister to the monophyletic Odonata. In addition, a sister group relationship between Palaeoptera and Neoptera was supported by the current mitogenomic data. Te acquisition of wings and of ability of fight contribute to the success of insects in the planet. -
Geographical Variation in the Wing Morphology of the Golden-Ringed
Bull. Natl. Mus. Nat. Sci., Ser. A, 38(2), pp. 65–73, May 22, 2012 Geographical Variation in the Wing Morphology of the Golden-ringed Dragonfly Anotogaster sieboldii (Selys, 1854) (Odonata, Cordulegastridae) Detected by Landmark-based Geometric Morphometrics Takuya Kiyoshi1 and Tsutomu Hikida2 1 Department of Zoology, National Museum of Nature and Science, 4–1–1 Amakubo, Tsukuba, Ibaraki, 305–0005 Japan E-mail: [email protected] 2 Department of Zoology, Graduate School of Science, Kyoto University, Kitashirakawaoiwakecho, Sakyo-ku, Kyoto, Kyoto, 606–8502 Japan (Received 18 January 2012; accepted 4 April 2012) Abstract A previous molecular phylogenetic study showed that Anotogaster sieboldii has at least 6 monophyletic groups that are allopatrically distributed in the northern area of Asia (Japanese main islands and Korean Peninsula), Amamioshima, Okinawajima, Yaeyama islands, Taiwan and East China. These groups are difficult to distinguish by qualitative genital morphology; however, canonical variate analysis and linear discriminant analysis of the hind wing shape have been used to clearly distinguish them from each other. In the present study, multiple comparisons of the lengths of the abdomen and hind wing showed that these lengths did not differ significantly among the groups. In particular, the variation in the size range, in the lineage from the northern area, widely overlapped that of the lineages from the other areas. In evaluating the morphological differ- ences, the wing shape was found to be more sensitive than other size variables. Key words : geometric morphometrics, shape, Odonata. Introduction groups (Askew, 2004). Anotogaster sieboldii (Selys, 1854) is a large The family Cordulegastridae of the order Odo- cordulegastrid dragonfly that is distributed in nata consists of 40 species belonging to 5 genera Insular East Asia, Korean Peninsula and East (Tsuda, 2000). -
Entomology of the Aucklands and Other Islands South of New Zealand: Lepidoptera, Ex Cluding Non-Crambine Pyralidae
Pacific Insects Monograph 27: 55-172 10 November 1971 ENTOMOLOGY OF THE AUCKLANDS AND OTHER ISLANDS SOUTH OF NEW ZEALAND: LEPIDOPTERA, EX CLUDING NON-CRAMBINE PYRALIDAE By J. S. Dugdale1 CONTENTS Introduction 55 Acknowledgements 58 Faunal Composition and Relationships 58 Faunal List 59 Key to Families 68 1. Arctiidae 71 2. Carposinidae 73 Coleophoridae 76 Cosmopterygidae 77 3. Crambinae (pt Pyralidae) 77 4. Elachistidae 79 5. Geometridae 89 Hyponomeutidae 115 6. Nepticulidae 115 7. Noctuidae 117 8. Oecophoridae 131 9. Psychidae 137 10. Pterophoridae 145 11. Tineidae... 148 12. Tortricidae 156 References 169 Note 172 Abstract: This paper deals with all Lepidoptera, excluding the non-crambine Pyralidae, of Auckland, Campbell, Antipodes and Snares Is. The native resident fauna of these islands consists of 42 species of which 21 (50%) are endemic, in 27 genera, of which 3 (11%) are endemic, in 12 families. The endemic fauna is characterised by brachyptery (66%), body size under 10 mm (72%) and concealed, or strictly ground- dwelling larval life. All species can be related to mainland forms; there is a distinctive pre-Pleistocene element as well as some instances of possible Pleistocene introductions, as suggested by the presence of pairs of species, one member of which is endemic but fully winged. A graph and tables are given showing the composition of the fauna, its distribution, habits, and presumed derivations. Host plants or host niches are discussed. An additional 7 species are considered to be non-resident waifs. The taxonomic part includes keys to families (applicable only to the subantarctic fauna), and to genera and species. -
Development of Microsatellite Markers for a Giant Water Bug, Appasus
1 Title: Development of microsatellite markers for a giant water bug, Appasus 2 japonicus, distributed in East Asia 3 4 Authors: Tomoya Suzuki,1* Akira S. Hirao,2,3 Masaki Takenaka,4 Koki Yano,5 Koji 5 Tojo1,6,* 6 7 1FaCulty of SCience, Shinshu University, Asahi 3-1-1, Matsumoto, Nagano 390-8621, 8 Japan 9 2Sugadaira Research Station, Mountain SCience Center, University of Tsukuba, 10 Sugadairakogen 1278-294, Ueda, Nagano 386-2204, Japan 11 3FaCulty of SymbiotiC Systems SCience, Fukushima University, Kanayagawa 1, 12 Fukushima, Fukushima 960-1296, Japan 13 4Division of Evolutionary Developmental Biology, National Institute for BasiC Biology, 14 Nishigonaka 38, Myodaiji, Okazaki, AiChi 44-8585, Japan 15 5Department of Mountain and Environmental SCience, InterdisCiplinary Graduate 16 SChool of SCience and TeChnology, Shinshu University, Asahi 3-1-1, Matsumoto, 17 Nagano 390-8621, Japan 18 6Institute of Mountain SCience, Shinshu University, Asahi 3-1-1, Matsumoto, Nagano 19 390-8621, Japan 20 21 *Corresponding authors 22 Koji Tojo: [email protected] 23 Tomoya Suzuki: [email protected] 24 25 26 1 1 Abstract 2 We developed miCrosatellite markers for Appasus japonicus (Hemiptera: 3 Belostomatidae). This belostomatid bug is distributed in East Asia (Japanese 4 Archipelago, Korean Peninsula, and Mainland China), and often listed as endangered 5 speCies in the ‘Red List’ or the ‘Red Data Book’ at the national and local level in Japan. 6 Here we desCribe twenty novel polymorphiC miCrosatellite loci developed for A. 7 japonicus, and marker suitability was evaluated on 56 individuals from four A. 8 japonicus populations (Nagano, Hiroshima, and Yamaguchi prefeCture, Japan, and 9 Chungcheongnam-do, Korea). -
Lepidoptera of North America 5
Lepidoptera of North America 5. Contributions to the Knowledge of Southern West Virginia Lepidoptera Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Lepidoptera of North America 5. Contributions to the Knowledge of Southern West Virginia Lepidoptera by Valerio Albu, 1411 E. Sweetbriar Drive Fresno, CA 93720 and Eric Metzler, 1241 Kildale Square North Columbus, OH 43229 April 30, 2004 Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Cover illustration: Blueberry Sphinx (Paonias astylus (Drury)], an eastern endemic. Photo by Valeriu Albu. ISBN 1084-8819 This publication and others in the series may be ordered from the C.P. Gillette Museum of Arthropod Diversity, Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, CO 80523 Abstract A list of 1531 species ofLepidoptera is presented, collected over 15 years (1988 to 2002), in eleven southern West Virginia counties. A variety of collecting methods was used, including netting, light attracting, light trapping and pheromone trapping. The specimens were identified by the currently available pictorial sources and determination keys. Many were also sent to specialists for confirmation or identification. The majority of the data was from Kanawha County, reflecting the area of more intensive sampling effort by the senior author. This imbalance of data between Kanawha County and other counties should even out with further sampling of the area. Key Words: Appalachian Mountains, -
Rhizopogon Togasawariana Sp. Nov., the First Report of Rhizopogon Associated with an Asian Species of Pseudotsuga
Rhizopogon togasawariana sp. nov., the first report of Rhizopogon associated with an Asian species of Pseudotsuga Mujic, A. B., Hosaka, K., & Spatafora, J. W. (2014). Rhizopogon togasawariana sp. nov., the first report of Rhizopogon associated with an Asian species of Pseudotsuga. Mycologia, 106(1), 105-112. doi:10.3852/13-055 10.3852/13-055 Allen Press Inc. Version of Record http://hdl.handle.net/1957/47245 http://cdss.library.oregonstate.edu/sa-termsofuse Mycologia, 106(1), 2014, pp. 105–112. DOI: 10.3852/13-055 # 2014 by The Mycological Society of America, Lawrence, KS 66044-8897 Rhizopogon togasawariana sp. nov., the first report of Rhizopogon associated with an Asian species of Pseudotsuga Alija B. Mujic1 the natural and anthropogenic range of the family Department of Botany and Plant Pathology, Oregon and plays an important ecological role in the State University, Corvallis, Oregon 97331-2902 establishment and maintenance of forests (Tweig et Kentaro Hosaka al. 2007, Simard 2009). The foundational species Department of Botany, National Museum of Nature concepts for genus Rhizopogon were established in the and Science, Tsukuba-shi, Ibaraki, 305-0005, Japan North American monograph of Smith and Zeller (1966), and a detailed monograph also has been Joseph W. Spatafora produced for European Rhizopogon species (Martı´n Department of Botany and Plant Pathology, Oregon 1996). However, few data on Asian species of State University, Corvallis, Oregon 97331-2902 Rhizopogon have been incorporated into phylogenetic and taxonomic studies and only a limited account of Asian Rhizopogon species has been published for EM Abstract: Rhizopogon subgenus Villosuli are the only associates of Pinus (Hosford and Trappe 1988). -
Biodiversity Conservation in Botanical Gardens
AgroSMART 2019 International scientific and practical conference ``AgroSMART - Smart solutions for agriculture'' Volume 2019 Conference Paper Biodiversity Conservation in Botanical Gardens: The Collection of Pinaceae Representatives in the Greenhouses of Peter the Great Botanical Garden (BIN RAN) E M Arnautova and M A Yaroslavceva Department of Botanical garden, BIN RAN, Saint-Petersburg, Russia Abstract The work researches the role of botanical gardens in biodiversity conservation. It cites the total number of rare and endangered plants in the greenhouse collection of Peter the Great Botanical garden (BIN RAN). The greenhouse collection of Pinaceae representatives has been analysed, provided with a short description of family, genus and certain species, presented in the collection. The article highlights the importance of Pinaceae for various industries, decorative value of plants of this group, the worth of the pinaceous as having environment-improving properties. In Corresponding Author: the greenhouses there are 37 species of Pinaceae, of 7 geni, all species have a E M Arnautova conservation status: CR -- 2 species, EN -- 3 species, VU- 3 species, NT -- 4 species, LC [email protected] -- 25 species. For most species it is indicated what causes depletion. Most often it is Received: 25 October 2019 the destruction of natural habitats, uncontrolled clearance, insect invasion and diseases. Accepted: 15 November 2019 Published: 25 November 2019 Keywords: biodiversity, botanical gardens, collections of tropical and subtropical plants, Pinaceae plants, conservation status Publishing services provided by Knowledge E E M Arnautova and M A Yaroslavceva. This article is distributed under the terms of the Creative Commons 1. Introduction Attribution License, which permits unrestricted use and Nowadays research of biodiversity is believed to be one of the overarching goals for redistribution provided that the original author and source are the modern world. -
Giant Water Bugs (Hemiptera: Heteroptera: Belostomatidae) of Israel
ISRAEL JOURNAL OF ENTOMOLOGY, Vol. 48 (1), pp. 119–141 (30 December 2018) A review of the giant water bugs (Hemiptera: Heteroptera: Nepomorpha: Belostomatidae) of Israel TANYA NOVOSELSKY 1, PING -P ING CHEN 2 & NI C O NIESER 2 1The Steinhardt Museum of Natural History, Israel National Center for Biodiversity Studies, Tel Aviv University, Tel Aviv 69978, Israel. E-mail: [email protected] 2Naturalis Biodiversity Centre, P.O. Box 9517, 2300 RA Leiden, The Netherlands. E-mail: [email protected], [email protected] ABSTRACT An updated and annotated check-list of Israeli giant water bugs (Belostomatidae) is provided. The recorded species belong in the subfamilies Belostomatinae and Lethocerinae. The following six species occur in the country: Appasus urinator urinator, Limnogeton fieberi, Lethocerus patruelis, Lethocerus cordofanus (new record), Hydrocyrius colombiae colombiae (new record) and Belostoma bifo ve olatum (new record). Belostoma bifoveolatum was previously known only from South America, so it is recorded in the Old World for the first time. An illustrated identification key is compiled for the Israeli Belostomatidae species. A list of exotic Belostomatidae material accumulated in the collection of the Steinhardt Museum of Natural History is provided. KEYWORDS: Hemiptera, Heteroptera, Nepomorpha, Belostomatidae, aquatic in sects, giant water bugs, identification key, male genitalia, Middle East, ta xonomy. INTRODUCTION The Belostomatidae is a family of aquatic heteropterans of almost world-wide distribution, although its greatest diversity is observed in the tropics (Merritt & Cummins 1996; Schuh & Slater 1995). The family includes the largest—up to 120 mm long—representatives of Heteroptera, which are known as the giant water bugs or electric-light bugs, because they are attracted to light sources at night (Ri- beiro et al. -
ISTA List of Stabilized Plant Names 7Th Edition
ISTA List of Stabilized Plant Names th 7 Edition ISTA Nomenclature Committee Chair: Dr. M. Schori Published by All rights reserved. No part of this publication may be The Internation Seed Testing Association (ISTA) reproduced, stored in any retrieval system or transmitted Zürichstr. 50, CH-8303 Bassersdorf, Switzerland in any form or by any means, electronic, mechanical, photocopying, recording or otherwise, without prior ©2020 International Seed Testing Association (ISTA) permission in writing from ISTA. ISBN 978-3-906549-77-4 ISTA List of Stabilized Plant Names 1st Edition 1966 ISTA Nomenclature Committee Chair: Prof P. A. Linehan 2nd Edition 1983 ISTA Nomenclature Committee Chair: Dr. H. Pirson 3rd Edition 1988 ISTA Nomenclature Committee Chair: Dr. W. A. Brandenburg 4th Edition 2001 ISTA Nomenclature Committee Chair: Dr. J. H. Wiersema 5th Edition 2007 ISTA Nomenclature Committee Chair: Dr. J. H. Wiersema 6th Edition 2013 ISTA Nomenclature Committee Chair: Dr. J. H. Wiersema 7th Edition 2019 ISTA Nomenclature Committee Chair: Dr. M. Schori 2 7th Edition ISTA List of Stabilized Plant Names Content Preface .......................................................................................................................................................... 4 Acknowledgements ....................................................................................................................................... 6 Symbols and Abbreviations .......................................................................................................................... -
Phragmites Australis
Journal of Ecology 2017, 105, 1123–1162 doi: 10.1111/1365-2745.12797 BIOLOGICAL FLORA OF THE BRITISH ISLES* No. 283 List Vasc. PI. Br. Isles (1992) no. 153, 64,1 Biological Flora of the British Isles: Phragmites australis Jasmin G. Packer†,1,2,3, Laura A. Meyerson4, Hana Skalov a5, Petr Pysek 5,6,7 and Christoph Kueffer3,7 1Environment Institute, The University of Adelaide, Adelaide, SA 5005, Australia; 2School of Biological Sciences, The University of Adelaide, Adelaide, SA 5005, Australia; 3Institute of Integrative Biology, Department of Environmental Systems Science, Swiss Federal Institute of Technology (ETH) Zurich, CH-8092, Zurich,€ Switzerland; 4University of Rhode Island, Natural Resources Science, Kingston, RI 02881, USA; 5Institute of Botany, Department of Invasion Ecology, The Czech Academy of Sciences, CZ-25243, Pruhonice, Czech Republic; 6Department of Ecology, Faculty of Science, Charles University, CZ-12844, Prague 2, Czech Republic; and 7Centre for Invasion Biology, Department of Botany and Zoology, Stellenbosch University, Matieland 7602, South Africa Summary 1. This account presents comprehensive information on the biology of Phragmites australis (Cav.) Trin. ex Steud. (P. communis Trin.; common reed) that is relevant to understanding its ecological char- acteristics and behaviour. The main topics are presented within the standard framework of the Biologi- cal Flora of the British Isles: distribution, habitat, communities, responses to biotic factors and to the abiotic environment, plant structure and physiology, phenology, floral and seed characters, herbivores and diseases, as well as history including invasive spread in other regions, and conservation. 2. Phragmites australis is a cosmopolitan species native to the British flora and widespread in lowland habitats throughout, from the Shetland archipelago to southern England. -
Latitudinal Gradient in Leaf Defense Traits of Woody Plants Along Japanese Archipelago
Latitudinal gradient in leaf defense traits of woody plants along Japanese archipelago 日本産樹木種における、葉防御形質の緯度傾度 Saihanna 1 General Introduction It is estimated that over the twenty million species of organisms are living on our planet, and all of these organisms adapted to their own living environment, namely niche (Hatchinson 1957). Not only the abiotic factors but biotic interaction plays a key role in the maintenance of biodiversity. Animal-plant interactions are one of the most important topic in community ecology (e.g. Morin 1999). Plants and herbivore insects have accounted for about half of the entire diversity on the earth (Strong et al., 1984). Plant-herbivore interactions are extremely complex, which should lead the tremendous diversity of both plants and herbivores (e.g. Gutierrez et al., 1984; Hay et al., 1989). Although the interaction between these two components, namely co-speciation, should account for this diversification, most of the studies so far, tend to explain this interaction only from one side of them. Plants have interacted with insect herbivores for several hundred million years, which should lead to complex defense systems against various herbivores (Fürstenberg-Hägg et al., 2013). This interaction between plants and herbivores has long proposed the opportunity for studying the mechanism of the creation and maintenance of biological diversity because of its universality and generality (Strong et al. 1984; Ali and Agrawal 2012). It is believed that the evolution of plant defense traits followed by counter-adaptations in herbivores could lead to bursts of adaptive radiation of both components (Ehrlich and Raven 1969). Understanding the coevolution of plant and insect species and macroevolution of adaptive traits has inspired biologists for some decades, yet has been challenging to study even present days (Schluter, 2000). -
Download This Article in PDF Format
Knowl. Manag. Aquat. Ecosyst. 2018, 419, 42 Knowledge & © K. Pabis, Published by EDP Sciences 2018 Management of Aquatic https://doi.org/10.1051/kmae/2018030 Ecosystems www.kmae-journal.org Journal fully supported by Onema REVIEW PAPER What is a moth doing under water? Ecology of aquatic and semi-aquatic Lepidoptera Krzysztof Pabis* Department of Invertebrate Zoology and Hydrobiology, University of Lodz, Banacha 12/16, 90-237 Lodz, Poland Abstract – This paper reviews the current knowledge on the ecology of aquatic and semi-aquatic moths, and discusses possible pre-adaptations of the moths to the aquatic environment. It also highlights major gaps in our understanding of this group of aquatic insects. Aquatic and semi-aquatic moths represent only a tiny fraction of the total lepidopteran diversity. Only about 0.5% of 165,000 known lepidopterans are aquatic; mostly in the preimaginal stages. Truly aquatic species can be found only among the Crambidae, Cosmopterigidae and Erebidae, while semi-aquatic forms associated with amphibious or marsh plants are known in thirteen other families. These lepidopterans have developed various strategies and adaptations that have allowed them to stay under water or in close proximity to water. Problems of respiratory adaptations, locomotor abilities, influence of predators and parasitoids, as well as feeding preferences are discussed. Nevertheless, the poor knowledge on their biology, life cycles, genomics and phylogenetic relationships preclude the generation of fully comprehensive evolutionary scenarios. Keywords: Lepidoptera / Acentropinae / caterpillars / freshwater / herbivory Résumé – Que fait une mite sous l'eau? Écologie des lépidoptères aquatiques et semi-aquatiques. Cet article passe en revue les connaissances actuelles sur l'écologie des mites aquatiques et semi-aquatiques, et discute des pré-adaptations possibles des mites au milieu aquatique.