Preliminary Swaziland Moths Checklist - PROVISIONAL - November 2018
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ARTHROPOD COMMUNITIES and PASSERINE DIET: EFFECTS of SHRUB EXPANSION in WESTERN ALASKA by Molly Tankersley Mcdermott, B.A./B.S
Arthropod communities and passerine diet: effects of shrub expansion in Western Alaska Item Type Thesis Authors McDermott, Molly Tankersley Download date 26/09/2021 06:13:39 Link to Item http://hdl.handle.net/11122/7893 ARTHROPOD COMMUNITIES AND PASSERINE DIET: EFFECTS OF SHRUB EXPANSION IN WESTERN ALASKA By Molly Tankersley McDermott, B.A./B.S. A Thesis Submitted in Partial Fulfillment of the Requirements for the Degree of Master of Science in Biological Sciences University of Alaska Fairbanks August 2017 APPROVED: Pat Doak, Committee Chair Greg Breed, Committee Member Colleen Handel, Committee Member Christa Mulder, Committee Member Kris Hundertmark, Chair Department o f Biology and Wildlife Paul Layer, Dean College o f Natural Science and Mathematics Michael Castellini, Dean of the Graduate School ABSTRACT Across the Arctic, taller woody shrubs, particularly willow (Salix spp.), birch (Betula spp.), and alder (Alnus spp.), have been expanding rapidly onto tundra. Changes in vegetation structure can alter the physical habitat structure, thermal environment, and food available to arthropods, which play an important role in the structure and functioning of Arctic ecosystems. Not only do they provide key ecosystem services such as pollination and nutrient cycling, they are an essential food source for migratory birds. In this study I examined the relationships between the abundance, diversity, and community composition of arthropods and the height and cover of several shrub species across a tundra-shrub gradient in northwestern Alaska. To characterize nestling diet of common passerines that occupy this gradient, I used next-generation sequencing of fecal matter. Willow cover was strongly and consistently associated with abundance and biomass of arthropods and significant shifts in arthropod community composition and diversity. -
126 Trichopterygini, and Nacophorini. Biodiversity
Trichopterygini, and Nacophorini. Biodiversity Nothofagus with molecular re-identification of the assessments were performed in Tasmania (January larvae from the COI profile. Gut content of the larvae 2006) and Chile (January 2008) with a collecting was analysed with various chloroplast markers for success of approx. 130 geometrid species for both verification of feeding on the host-plant. The pilot countries. COI barcode profiles were generated study revealed to be most successful with the psbA- for the geometrids of both countries. 85 specimens trnH marker, at a success of 8/13 larvae. In the main belonging to 75 target species were analysed with project the number of investigated taxa and markers the additional nuclear markers EF1alpha and 28S shall be increased, the larval assessment intensified for an integrative morphological-molecular analysis and a molecular clock approach performed by us- and for building a more robust phylogenetic tree. ing various calibration models for the dating of the Assessment of geometrid larvae was tested through divergences in the phylogenetic tree. traditional collecting and canopy fogging on Chilean Revision of the genus Cyllopoda Delano Lewis Lewis, D. (2009): Revision of the genus Cyllopoda. Pp. 126 in: Hausmann, A. (ed.): Proceedings of the fifth Forum Herbulot 2008. Global strategies for plotting ge- ometrid biodiversity in web-based databases (Munich, ZSM, 24-28 June 2008). – Spixiana 32/1: 126 Delano Lewis, McGuire Center for Lepidoptera and Biodiversity, Florida Mu- seum of Natural History, 34th Street and Hull Road, P.O. Box 112710, Gainesville FL 32611, U.S.A.; e-mail: [email protected] In this revision, some of the synonymy that exists Cyllopoda osiris osiris and Cyllopoda osiris protmeta; in the genus Cyllopoda is resolved and a contribu- the designation of a neotype for Cyllopoda osiris; tion to a better understanding of the relationships the designation of lectotypes for Cyllopoda angusta, within this genus is accomplished. -
(Lepidoptera: Tortricidae) from the Sky Islands of Southeastern Arizona
NUv 2 RECD PROC. ENTOMOL. SOC. WASH. 111(4). 2009, pp. 769-774 A NEW SPECIES OF CLEPSIS GUENEE, 1845 (LEPIDOPTERA: TORTRICIDAE) FROM THE SKY ISLANDS OF SOUTHEASTERN ARIZONA JASON J. DOMBROSKIE AND JOHN W. BROWN (JJD) Department of Biological Sciences, University of Alberta T6G 2E9, Canada (e-mail: dornbrosk(i-b ualberta.ca); (J W B) Systematic Entomology Labora- tory, PSI, Agricultural Research Service, U.S. Department of Agriculture, National Museum of Natural History, Washington, DC 20013-7012 U.S.A. (e-mail: john. brown @ars.usda.gov ) Abstract.—Clepsis anderslaneyii, new species is described and illustrated from the "sky islands" (i.e., Chiricahua, Huachuca, and Santa Rita mountains) of southeastern Arizona, U.S.A. Superficially, it is most similar to Argvrotac'nia dorsafana (Dyar 1903), but it is assigned unambiguously to Clepsis Guenée on the basis of the characteristically modified transtilla, which includes a narrow or obsolete mesal portion and a dentate subbasal swollen lobe. Among Nearctic congeners, the male genitalia of C. anderslanevii are most similar to those of C. fucana (Walsingham 1879), but those of C anderslanevii can be distinguished by the more broadly pointed valva, narrower transtilla, bulbous uncus, and broader tegumen. The extremely short ductus bursae of the female genitalia of C. andersianevu is unique among Clepsis. Key Words: Archipini, genitalia, Madrean, Nearctic, systematics Clepsis Guenée, encompassing 144 and Santa Rita mountains), known as described species, is present in every the "sky islands," are of considerable major zoogeographic region except the interest to biologists and hiogeogra- Australasian (sensu Heppner 1991). The phers. These montane "islands" are genus is most diverse in the Holarctic forested ranges separated by a lowland and Neotropical regions (Brown 2005, "sea" of desert and grassland. -
The Entomofauna on Eucalyptus in Israel: a Review
EUROPEAN JOURNAL OF ENTOMOLOGYENTOMOLOGY ISSN (online): 1802-8829 Eur. J. Entomol. 116: 450–460, 2019 http://www.eje.cz doi: 10.14411/eje.2019.046 REVIEW The entomofauna on Eucalyptus in Israel: A review ZVI MENDEL and ALEX PROTASOV Department of Entomology, Institute of Plant Protection, Agricultural Research Organization, The Volcani Center, Rishon LeTzion 7528809, Israel; e-mails: [email protected], [email protected] Key words. Eucalyptus, Israel, invasive species, native species, insect pests, natural enemies Abstract. The fi rst successful Eucalyptus stands were planted in Israel in 1884. This tree genus, particularly E. camaldulensis, now covers approximately 11,000 ha and constitutes nearly 4% of all planted ornamental trees. Here we review and discuss the information available about indigenous and invasive species of insects that develop on Eucalyptus trees in Israel and the natural enemies of specifi c exotic insects of this tree. Sixty-two phytophagous species are recorded on this tree of which approximately 60% are indigenous. The largest group are the sap feeders, including both indigenous and invasive species, which are mostly found on irrigated trees, or in wetlands. The second largest group are wood feeders, polyphagous Coleoptera that form the dominant native group, developing in dying or dead wood. Most of the seventeen parasitoids associated with the ten invasive Eucalyptus-specifi c species were introduced as biocontrol agents in classical biological control projects. None of the polyphagous species recorded on Eucalyptus pose any threat to this tree. The most noxious invasive specifi c pests, the gall wasps (Eulophidae) and bronze bug (Thaumastocoris peregrinus), are well controlled by introduced parasitoids. -
Biodiversity, Evolution and Ecological Specialization of Baculoviruses: A
Biodiversity, Evolution and Ecological Specialization of Baculoviruses: A Treasure Trove for Future Applied Research Julien Thézé, Carlos Lopez-Vaamonde, Jenny Cory, Elisabeth Herniou To cite this version: Julien Thézé, Carlos Lopez-Vaamonde, Jenny Cory, Elisabeth Herniou. Biodiversity, Evolution and Ecological Specialization of Baculoviruses: A Treasure Trove for Future Applied Research. Viruses, MDPI, 2018, 10 (7), pp.366. 10.3390/v10070366. hal-02140538 HAL Id: hal-02140538 https://hal.archives-ouvertes.fr/hal-02140538 Submitted on 26 May 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Distributed under a Creative Commons Attribution| 4.0 International License viruses Article Biodiversity, Evolution and Ecological Specialization of Baculoviruses: A Treasure Trove for Future Applied Research Julien Thézé 1,2, Carlos Lopez-Vaamonde 1,3 ID , Jenny S. Cory 4 and Elisabeth A. Herniou 1,* ID 1 Institut de Recherche sur la Biologie de l’Insecte, UMR 7261, CNRS—Université de Tours, 37200 Tours, France; [email protected] (J.T.); [email protected] -
Noctuoidea: Erebidae: Others
Staude et al. / Metamorphosis 27: S165–S188 S165 ____________________________________________________________________________________________________________________________ Noctuoidea: Erebidae: Others Reference/ Lepidoptera Host plant Locality rearing no. Taxon Subfamily Family Taxon Family M1148 Anoba angulilinea Anobinae Erebidae Dalbergia Fabaceae Tshukudu Game melanoxylon Reserve, Hoedspruit M998 Anoba atripuncta Anobinae Erebidae Ormocarpum Fabaceae Tshukudu Game trichocarpum Reserve, Hoedspruit Gv71 Baniana arvorum Anobinae Erebidae Elephantorrhiza Fabaceae Steenkoppies, farm, elephantina Magaliesburg 14HSS52 Baniana arvorum Anobinae Erebidae Elephantorrhiza Fabaceae Steenkoppies, farm, elephantina Magaliesburg 13HSS84 Plecoptera arctinotata Anobinae Erebidae Senegalia caffra Fabaceae Steenkoppies, farm, Magaliesburg M1020a Plecoptera flaviceps Anobinae Erebidae Dalbergia Fabaceae Casketts, farm, melanoxylon Hoedspruit M317 Bareia incidens Calpinae Erebidae Ficus lutea Moraceae Casketts, farm, (unplaced as to Hoedspruit tribe) 14HSS87 Egnasia vicaria Calpinae Erebidae Afrocanthium Rubiaceae Dlinsa Forest, (unplaced as to mundianum Eshowe tribe) 12HSS163 Exophyla multistriata Calpinae Erebidae Celtis africana Cannabaceae Golden Valley, (unplaced as to Magaliesburg tribe) M416 Exophyla multistriata Calpinae Erebidae Trema orientalis Cannabaceae Sekororo, Tzaneen (unplaced as to (Fed on Celtis tribe) africana) M743 Lacera alope Calpinae Erebidae Pterolobium Fabaceae Moholoholo Rehab (unplaced as to stellatum Centre, Hoedspruit tribe) -
Report-VIC-Croajingolong National Park-Appendix A
Croajingolong National Park, Victoria, 2016 Appendix A: Fauna species lists Family Species Common name Mammals Acrobatidae Acrobates pygmaeus Feathertail Glider Balaenopteriae Megaptera novaeangliae # ~ Humpback Whale Burramyidae Cercartetus nanus ~ Eastern Pygmy Possum Canidae Vulpes vulpes ^ Fox Cervidae Cervus unicolor ^ Sambar Deer Dasyuridae Antechinus agilis Agile Antechinus Dasyuridae Antechinus mimetes Dusky Antechinus Dasyuridae Sminthopsis leucopus White-footed Dunnart Felidae Felis catus ^ Cat Leporidae Oryctolagus cuniculus ^ Rabbit Macropodidae Macropus giganteus Eastern Grey Kangaroo Macropodidae Macropus rufogriseus Red Necked Wallaby Macropodidae Wallabia bicolor Swamp Wallaby Miniopteridae Miniopterus schreibersii oceanensis ~ Eastern Bent-wing Bat Muridae Hydromys chrysogaster Water Rat Muridae Mus musculus ^ House Mouse Muridae Rattus fuscipes Bush Rat Muridae Rattus lutreolus Swamp Rat Otariidae Arctocephalus pusillus doriferus ~ Australian Fur-seal Otariidae Arctocephalus forsteri ~ New Zealand Fur Seal Peramelidae Isoodon obesulus Southern Brown Bandicoot Peramelidae Perameles nasuta Long-nosed Bandicoot Petauridae Petaurus australis Yellow Bellied Glider Petauridae Petaurus breviceps Sugar Glider Phalangeridae Trichosurus cunninghami Mountain Brushtail Possum Phalangeridae Trichosurus vulpecula Common Brushtail Possum Phascolarctidae Phascolarctos cinereus Koala Potoroidae Potorous sp. # ~ Long-nosed or Long-footed Potoroo Pseudocheiridae Petauroides volans Greater Glider Pseudocheiridae Pseudocheirus peregrinus -
Lepidoptera: Tortricidae: Tortricinae) and Evolutionary Correlates of Novel Secondary Sexual Structures
Zootaxa 3729 (1): 001–062 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Monograph ZOOTAXA Copyright © 2013 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3729.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:CA0C1355-FF3E-4C67-8F48-544B2166AF2A ZOOTAXA 3729 Phylogeny of the tribe Archipini (Lepidoptera: Tortricidae: Tortricinae) and evolutionary correlates of novel secondary sexual structures JASON J. DOMBROSKIE1,2,3 & FELIX A. H. SPERLING2 1Cornell University, Comstock Hall, Department of Entomology, Ithaca, NY, USA, 14853-2601. E-mail: [email protected] 2Department of Biological Sciences, University of Alberta, Edmonton, Canada, T6G 2E9 3Corresponding author Magnolia Press Auckland, New Zealand Accepted by J. Brown: 2 Sept. 2013; published: 25 Oct. 2013 Licensed under a Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0 JASON J. DOMBROSKIE & FELIX A. H. SPERLING Phylogeny of the tribe Archipini (Lepidoptera: Tortricidae: Tortricinae) and evolutionary correlates of novel secondary sexual structures (Zootaxa 3729) 62 pp.; 30 cm. 25 Oct. 2013 ISBN 978-1-77557-288-6 (paperback) ISBN 978-1-77557-289-3 (Online edition) FIRST PUBLISHED IN 2013 BY Magnolia Press P.O. Box 41-383 Auckland 1346 New Zealand e-mail: [email protected] http://www.mapress.com/zootaxa/ © 2013 Magnolia Press 2 · Zootaxa 3729 (1) © 2013 Magnolia Press DOMBROSKIE & SPERLING Table of contents Abstract . 3 Material and methods . 6 Results . 18 Discussion . 23 Conclusions . 33 Acknowledgements . 33 Literature cited . 34 APPENDIX 1. 38 APPENDIX 2. 44 Additional References for Appendices 1 & 2 . 49 APPENDIX 3. 51 APPENDIX 4. 52 APPENDIX 5. -
Integrated Pest Management in the Global Arena
Integrated Pest Management in the Global Arena This Handbook is dedicated to all the participants of the Michigan State University’s International IPM Short Course and to the faculty members who have provided support to this course. Integrated Pest Management in the Global Arena Edited by K.M. Maredia Professor Institute of International Agriculture and Department of Entomology Michigan State University East Lansing Michigan USA D. Dakouo Senior Research Scientist INERA Bobo-Dioulasso Burkina Faso and D. Mota-Sanchez Research Associate Department of Entomology Michigan State University East Lansing Michigan USA CABI Publishing CABI Publishing is a division of CAB International CABI Publishing CABI Publishing CAB International 44 Brattle Street Wallingford 4th Floor Oxon OX10 8DE Cambridge, MA 02138 UK USA Tel: +44 (0)1491 832111 Tel: +1 617 395 4056 Fax: +44 (0)1491 833508 Fax: +1 617 354 6875 Email: [email protected] E-mail: [email protected] Website: www.cabi-publishing.org ©CAB International 2003. All rights reserved. No part of this publication may be reproduced in any form or by any means, electronically, mechanically, by photocopying, recording or otherwise, without the prior permission of the copyright owners. A catalogue record for this book is available from the British Library, London, UK. Library of Congress Cataloging-in-Publication Data Integrated pest management in the global arena /edited by K.M. Maredia, D. Dakouo, D. Mota-Sanchez p. cm. Includes bibliographical references. ISBN 0-85199-652-3 1. Pests--Integrated control. I. Maredia, Karim M. II. Dakouo, D. (Dona), 1951- III. Mota-Sanchez, D. (David), 1960- SB950.I4575 2003 632′.9--dc21 2002154965 ISBN 0 85199 652 3 Typeset by AMA DataSet, UK Printed and bound in the UK by Cromwell Press, Trowbridge Contents Contributors ix Preface xv Acknowledgments xvii Foreword xix Acronyms and Abbreviations xxi 1Introduction and Overview 1 K.M. -
Lepidoptera Fauna of Namibia. I. Seasonal Distribution of Moths of the Koakoland (Mopane) Savanna in Ogongo, Northern Namibia
FRAGMENTA FAUNISTICA 57 (2): 117–129, 2014 PL ISSN 0015-9301 © MUSEUM AND INSTITUTE OF ZOOLOGY PAS DOI 10.3161/00159301FF2014.57.2.117 Lepidoptera fauna of Namibia. I. Seasonal distribution of moths of the Koakoland (Mopane) Savanna in Ogongo, northern Namibia Grzegorz KOPIJ Department of Wildlife Management, University of Namibia, Katima Mulilio Campus, Private Bag 1096, Katima Mulilo, Namibia; e-mail: [email protected] Abstract: During the years 2011–2013, moths were collected in Koakoland (Mopane) Savanna in the Cuvelai Drainage System, Ovamboland, northern Namibia. In total, 77 species from 13 families have been identified. Their seasonal occurrence in this habitat was also investigated, with most species recorded in wet season between September and April, but with clear peak in February and March. The family Noctuidae was by far the most speciose (38 recorded species), followed by Crambidae (8 spp.), Sphingidae (6 spp.) and Arctiidae (4 spp.). All other families were represented by 1–3 species. For each species listed date of collection is given, and data on its global distribution. Key words: Lepidoptera, check-list, biodiversity, distribution, moths, Ovamboland INTRODUCTION According to recent quite precise estimate, there are 15 5181 species, 16 650 genera and 121 families of Lepidoptera worldwide (Pouge 2009). Lepidoptera fauna of Namibia has recently attracted attention of European entomologists. However, thorough surveys were conducted hitherto in a few areas only, such as Brandberg and Hobatere. The northern regions of the country were especially badly neglected. In southern Africa (south of Zambezi and Kunene Rivers) – 8 511 species, 2 368 genera and 89 families were recently catalogued (Vári et al. -
Small Ermine Moths Role of Pheromones in Reproductive Isolation and Speciation
CHAPTER THIRTEEN Small Ermine Moths Role of Pheromones in Reproductive Isolation and Speciation MARJORIE A. LIÉNARD and CHRISTER LÖFSTEDT INTRODUCTION Role of antagonists as enhancers of reproductive isolation and interspecific interactions THE EVOLUTION TOWARDS SPECIALIZED HOST-PLANT ASSOCIATIONS SUMMARY: AN EMERGING MODEL SYSTEM IN RESEARCH ON THE ROLE OF SEX PHEROMONES IN SPECIATION—TOWARD A NEW SEX PHEROMONES AND OTHER ECOLOGICAL FACTORS “SMALL ERMINE MOTH PROJECT”? INVOLVED IN REPRODUCTIVE ISOLATION Overcoming the system limitations Overview of sex-pheromone composition Possible areas of future study Temporal and behavioral niches contributing to species separation ACKNOWLEDGMENTS PHEROMONE BIOSYNTHESIS AND MODULATION REFERENCES CITED OF BLEND RATIOS MALE PHYSIOLOGICAL AND BEHAVIORAL RESPONSE Detection of pheromone and plant compounds Introduction onomic investigations were based on examination of adult morphological characters (e.g., wing-spot size and color, geni- Small ermine moths belong to the genus Yponomeuta (Ypo- talia) (Martouret 1966), which did not allow conclusive dis- nomeutidae) that comprises about 75 species distributed glob- crimination of all species, leading to recognition of the so- ally but mainly in the Palearctic region (Gershenson and called padellus-species complex (Friese 1960) which later Ulenberg 1998). These moths are a useful model to decipher proved to include five species (Wiegand 1962; Herrebout et al. the process of speciation, in particular the importance of eco- 1975; Povel 1984). logical adaptation driven by host-plant shifts and the utiliza- In the 1970s, “the small ermine moth project” was initiated tion of species-specific pheromone mating-signals as prezy- to include research on many aspects of the small ermine gotic reproductive isolating mechanisms. -
Scientific Note: Functional Morphology of Masquerading Larva of Ceratonyx Satanaria with Notes on Horned Spanworm, Nematocampa Resistaria (Geometridae: Ennominae)
SOURAKOV & STUBINA: Larva of Ceratonyx satanaria TROP. LEPID. RES., 22(1): 53-59, 2012 53 SCIENTIFIC NOTE: FUNCTIONAL MORPHOLOGY OF MASQUERADING LARVA OF CERATONYX SATANARIA WITH NOTES ON HORNED SPANWORM, NEMATOCAMPA RESISTARIA (GEOMETRIDAE: ENNOMINAE) Andrei Sourakov and Minna Stubina McGuire Center for Lepidoptera and Biodiversity, Florida Museum of Natural History, University of Florida, Gainesville, FL 32611; [email protected] Abstract - Morphological drawings and photographs are provided illustrating the unusual larval morphology, featuring long cervical horns or tubercles, of the geometrid moth Ceratonyx satanaria Guenée. In addition photographs of Nematocampa resistaria (Herrich-Schäffer) larvae, commonly known as a “horned spanworm” for its long abdominal tubercles, are also provided. The possible function of cervical horns is discussed in the context of predator-prey interactions. A survey of available photographs of geometrid larvae worldwide revealed cervical horns only in the genera Ceratonyx (Ennominae: Nacophorini) and in two Australian species of Geometridae: Plesanemma fucata (F&R 1875) (Ennominae: Nacophorini) and Parepisparis lutosaria (F. & R) (Oenochrominae). Key words: anti-predator defenses, mimicry, camouflage, crypsis. Larvae of Geometridae and genus Ceratonyx Morphology of Ceratonyx larvae The remarkable twig-like appearance of geometrid moth The larva illustrated in Figs. 1-2 was found on the ground larvae, and in particular the polymorphism and effectiveness in mid-April in Gainesville, Florida (Lat.: 29.6864; Long.: of this mode of defense against predators, has attracted much -82.3391”), and was preserved in 70% ethanol after boiling attention from researchers. While larval color can depend on in water. It measures 33 mm long, with cervical horns 10 mm diet, and hence can be regulated by environmental factors (e.g., long, and head 3.5 mm wide.