2008/2009 Annual Report Australian
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Stick Insects Fact Sheet
Stick Insects Fact Sheet Female Titan Stick Insect. Image: QM, Jeff Wright. Introduction Biology Stick and leaf insects, scientifically known as phasmids, Females lay eggs one at a time, often with a flick of their are among the largest of all insects in the world. At 26 cm, abdomens to throw the egg some distance. An individual the Titan Stick Insect (Acrophylla titan) is the longest of female drops eggs at a rate of one to several per day and all Australian insects. Phasmids have perfected the art of she can produce between 100 and 1,300 eggs in her life- camouflage. Some resemble sticks and foliage so closely time. They fall to the ground and lie in the leaf litter. they even feature false buds, thorns and ragged leaf-like flanges. Small wonder they are rarely seen except after storms when they are blown out of threes and shrubs. Phasmids are sometimes confused with a different group of insects, the mantids. Also called Praying Mantids, these are predators with large, spiny front legs, held folded ready to strike and grasp prey. In contrast, Phasmids are herbivores (plant-eaters) with simple front legs that are similar in size and structure to their other legs. A variety of insect eggs. (on left). An ant carrying a stick insect egg (on right). Images: QM, Jeff Wright. All stick insects feed on fresh leaves. Some browse on a wide variety of trees and shrubs but others are fussy, eating only a limited range of host plants that are often closely Stick insect eggs are generally oval, and superficially seed- related to each other. -
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). -
Species List January 28 – February 6, 2020 | Compiled by Keith Hansen
Guatemala: Nature & Culture With Tikal Extension| Species List January 28 – February 6, 2020 | Compiled by Keith Hansen With Guides Keith Hansen, Patricia Briceño, Roland Rumm and local guide Freddie and participants Julie, Paul, Gwen, Gary, Barbara, Rolande, Brian, Jane, and Debbie. Itinerary Day 1: 1/29/20, Guatemala City. Clarion Hotel to Marroquin University and Textile Museum, to Guatemala Market, to Cocales “Crazy Gas Station” at intersection of CA 12 and 11 to Los Tarrales Natural Reserve. Day 2: 1/30/20, Los Tarrales Nat. Res. into jeeps and up to La Isla vista point. Down for lunch at lodge. Then San Pedro trail and back to La Rinconada lodge, for dinner. Day 3: 1/31/20, Pre-dawn, Volcan Fuego eruption. Los Tarrales, short walk on San Pedro Trail. Breakfast at lodge. Depart and drive to Fuentes Georginia Hot Springs Spa. Lunch with “mega flock”. Depart and drive to Xela (Quetzaltenango). Dinner at Hotel Bonifaz. Day 4: 2/1/20, Split group. One group, (Keith), up at 4:00 AM. Drive to Refugio del Quetzal for Quetzal, then viewing from mirador “overlook”. Then drive to San Rafael for lunch. Then drive back to Xela. Second group, (Patricia) Xela tour. Later some went back to “Owl” at Fuentes Georgino Hot Springs, then back to Xela. Day 5: 2/2/20, Xela breakfast at Hotel, depart for the market at Chichicastenango with stop at Continental Divide at 10,000 feet. To market, then lunch at “Mayan Inn”. Drive to Panajachel at Lago de Atitlan. Boarded a launch to cross the lake to Hotel Bambu, Santiago Atitlan. -
Abstract Book
Welcome to the Ornithological Congress of the Americas! Puerto Iguazú, Misiones, Argentina, from 8–11 August, 2017 Puerto Iguazú is located in the heart of the interior Atlantic Forest and is the portal to the Iguazú Falls, one of the world’s Seven Natural Wonders and a UNESCO World Heritage Site. The area surrounding Puerto Iguazú, the province of Misiones and neighboring regions of Paraguay and Brazil offers many scenic attractions and natural areas such as Iguazú National Park, and provides unique opportunities for birdwatching. Over 500 species have been recorded, including many Atlantic Forest endemics like the Blue Manakin (Chiroxiphia caudata), the emblem of our congress. This is the first meeting collaboratively organized by the Association of Field Ornithologists, Sociedade Brasileira de Ornitologia and Aves Argentinas, and promises to be an outstanding professional experience for both students and researchers. The congress will feature workshops, symposia, over 400 scientific presentations, 7 internationally renowned plenary speakers, and a celebration of 100 years of Aves Argentinas! Enjoy the book of abstracts! ORGANIZING COMMITTEE CHAIR: Valentina Ferretti, Instituto de Ecología, Genética y Evolución de Buenos Aires (IEGEBA- CONICET) and Association of Field Ornithologists (AFO) Andrés Bosso, Administración de Parques Nacionales (Ministerio de Ambiente y Desarrollo Sustentable) Reed Bowman, Archbold Biological Station and Association of Field Ornithologists (AFO) Gustavo Sebastián Cabanne, División Ornitología, Museo Argentino -
For Peer Review Only
BIOTROPICA The relative contribut ion of specialists and generalists to mistletoe dispersal: insights from a Neotropical rainforest For Peer Review Only Journal: Biotropica Manuscript ID: BITR-11-411.R1 Manuscript Type: Paper Date Submitted by the Author: n/a Complete List of Authors: Watson, David; Charles Sturt University, The Johnstone Centre Barro Colorado Island, Frugivory and seed dispersal, Loranthaceae, Keywords: Tyrannidae, Foraging, Mionectes oleagineus, Miozetetes, Tyrannulus elatus, Zimmerius vilissimus Association for Tropical Biology and Conservation Page 1 of 34 BIOTROPICA 1 2 3 4 5 1 The relative contribution of specialists and generalists to mistletoe 6 7 8 2 dispersal: insights from a Neotropical rainforest 9 10 11 12 3 13 14 For Peer Review Only 15 4 DAVID M WATSON 16 17 18 5 Institute for Land Water and Society and School of Environmental Sciences 19 20 21 22 6 Charles Sturt University 23 24 25 7 PO Box 789 Albury 2640 Australia 26 27 28 8 29 30 31 9 Email [email protected] 32 33 34 10 35 36 37 38 11 Submitted as a standard paper to Biotropica 22 November 2011 39 40 41 12 Fully revised manuscript submitted 01 March 2012 42 43 44 13 45 46 47 14 Running head: Specialist vs generalist mistletoe dispersers 48 49 50 51 15 52 53 54 16 Received ____________; revision accepted ____________. 55 56 57 58 59 60 Association for Tropical Biology and Conservation BIOTROPICA Page 2 of 34 1 1 2 3 4 5 1 ABSTRACT 6 7 8 2 Mistletoes rely on birds for seed dispersal, but the presumed importance of mistletoe-specialist 9 10 3 frugivores has not been critically examined nor compared with generalist frugivores and 11 12 13 4 opportunistic foragers. -
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. -
Species Boundaries, Biogeography, and Intra-Archipelago Genetic Variation Within the Emoia Samoensis Species Group in the Vanuatu Archipelago and Oceania" (2008)
Louisiana State University LSU Digital Commons LSU Doctoral Dissertations Graduate School 2008 Species boundaries, biogeography, and intra- archipelago genetic variation within the Emoia samoensis species group in the Vanuatu Archipelago and Oceania Alison Madeline Hamilton Louisiana State University and Agricultural and Mechanical College, [email protected] Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_dissertations Recommended Citation Hamilton, Alison Madeline, "Species boundaries, biogeography, and intra-archipelago genetic variation within the Emoia samoensis species group in the Vanuatu Archipelago and Oceania" (2008). LSU Doctoral Dissertations. 3940. https://digitalcommons.lsu.edu/gradschool_dissertations/3940 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Doctoral Dissertations by an authorized graduate school editor of LSU Digital Commons. For more information, please [email protected]. SPECIES BOUNDARIES, BIOGEOGRAPHY, AND INTRA-ARCHIPELAGO GENETIC VARIATION WITHIN THE EMOIA SAMOENSIS SPECIES GROUP IN THE VANUATU ARCHIPELAGO AND OCEANIA A Dissertation Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Doctor of Philosophy in The Department of Biological Sciences by Alison M. Hamilton B.A., Simon’s Rock College of Bard, 1993 M.S., University of Florida, 2000 December 2008 ACKNOWLEDGMENTS I thank my graduate advisor, Dr. Christopher C. Austin, for sharing his enthusiasm for reptile diversity in Oceania with me, and for encouraging me to pursue research in Vanuatu. His knowledge of the logistics of conducting research in the Pacific has been invaluable to me during this process. -
Australian Sphingidae – DNA Barcodes Challenge Current Species Boundaries and Distributions
Australian Sphingidae – DNA Barcodes Challenge Current Species Boundaries and Distributions Rodolphe Rougerie1*¤, Ian J. Kitching2, Jean Haxaire3, Scott E. Miller4, Axel Hausmann5, Paul D. N. Hebert1 1 University of Guelph, Biodiversity Institute of Ontario, Guelph, Ontario, Canada, 2 Natural History Museum, Department of Life Sciences, London, United Kingdom, 3 Honorary Attache´, Muse´um National d’Histoire Naturelle de Paris, Le Roc, Laplume, France, 4 National Museum of Natural History, Smithsonian Institution, Washington, DC, United States of America, 5 Bavarian State Collection of Zoology, Section Lepidoptera, Munich, Germany Abstract Main Objective: We examine the extent of taxonomic and biogeographical uncertainty in a well-studied group of Australian Lepidoptera, the hawkmoths (Sphingidae). Methods: We analysed the diversity of Australian sphingids through the comparative analysis of their DNA barcodes, supplemented by morphological re-examinations and sequence information from a nuclear marker in selected cases. The results from the analysis of Australian sphingids were placed in a broader context by including conspecifics and closely related taxa from outside Australia to test taxonomic boundaries. Results: Our results led to the discovery of six new species in Australia, one case of erroneously synonymized species, and three cases of synonymy. As a result, we establish the occurrence of 75 species of hawkmoths on the continent. The analysis of records from outside Australia also challenges the validity of current taxonomic boundaries in as many as 18 species, including Agrius convolvuli (Linnaeus, 1758), a common species that has gained adoption as a model system. Our work has revealed a higher level of endemism than previously recognized. Most (90%) Australian sphingids are endemic to the continent (45%) or to Australia, the Pacific Islands and the Papuan and Wallacean regions (45%). -
Divergence in Gut Bacterial Community Among Life Stages of the Rainbow Stag Beetle Phalacrognathus Muelleri (Coleoptera: Lucanidae)
insects Article Divergence in Gut Bacterial Community Among Life Stages of the Rainbow Stag Beetle Phalacrognathus muelleri (Coleoptera: Lucanidae) 1,2, 1,2, 1,2, Miaomiao Wang y, Xingjia Xiang y and Xia Wan * 1 School of Resources and Environmental Engineering, Anhui University, Hefei 230601, China; [email protected] (M.W.); [email protected] (X.X.) 2 Anhui Province Key Laboratory of Wetland Ecosystem Protection and Restoration, Hefei 230601, China * Correspondence: [email protected] These authors contributed equally to this article. y Received: 19 September 2020; Accepted: 17 October 2020; Published: 21 October 2020 Simple Summary: Phalacrognathus muelleri is naturally distributed in Queensland (Australia) and New Guinea, and this species can be successfully bred under artificial conditions. In this study, we compared gut bacterial community structure among different life stages. There were dramatic shifts in gut bacterial community structure between larvae and adults, which was probably shaped by their diet. The significant differences between early instar and final instars larvae suggested that certain life stages are associated with a defined gut bacterial community. Our results contribute to a better understanding of the potential role of gut microbiota in a host’s growth and development, and the data will benefit stag beetle conservation in artificial feeding conditions. Abstract: Although stag beetles are popular saprophytic insects, there are few studies about their gut bacterial community. This study focused on the gut bacterial community structure of the rainbow stag beetle (i.e., Phalacrognathus muelleri) in its larvae (three instars) and adult stages, using high throughput sequencing (Illumina Miseq). Our aim was to compare the gut bacterial community structure among different life stages. -
Ecography E5383
Ecography E5383 Hamilton, A. M., Hartman, J. H. and Austin, C. C. 2009. Island area and species diversity in the southwest Pacific Ocean: is the lizard fauna of Vanuatu depauperate? – Ecography 32: 247– 258. Supplementary material Appendix 1. Species lists of lizards for island groups included in this analysis. Hemidactylus frenatus, H. garnotii, and Lepidodactylus lugubris are considered introduced to all island groups included in this comparison and therefore are not included below. This list represents a conservative estimate of the true native reptile diversity within each island group as we did not include currently undescribed taxa, and considered a species introduced if a previous worker indicated the distribution was likely the result of an introduction and provided supporting data. Endemic species have a distribution restricted to a single archipelago. We used published literature (published prior to 1 August 2008), personal field observations, and unpublished molecular data to develop this list; the primary source(s) for each record is included with the record and references are provided below the table. Solomon Fiji Archipelago Vanuatu Samoan Tongan New Caledonia Loyalty Islands Taxon Islands Archipelago Islands Archipelago AGAMIDAE Hypsilurus godeffroyi Native (1) DIPLODACTYLIDAE Bavayia crassicollis Native (18) Native (18) Bavayia cyclura Native (18) Native (18) Bavayia exsuccida Endemic (18) Bavayia geitaina Endemic (18) Bavayia goroensis Endemic (2) Bavayia madjo Endemic (18) Bavayia montana Endemic (18) Bavayia ornata Endemic -
Download Complete Work
© The Authors, 2015. Journal compilation © Australian Museum, Sydney, 2015 Records of the Australian Museum (2015) Vol. 67, issue number 7, pp. 207–224. ISSN 0067-1975 (print), ISSN 2201-4349 (online) http://dx.doi.org/10.3853/j.2201-4349.67.2015.1649 Taxonomic Resolution to the Problem of Polyphyly in the New Caledonian Scincid Lizard Genus Lioscincus (Squamata: Scincidae) ROSS A. SADLIER1*, AarON M. BAUER2, GLENN M. SHEA3,1 AND SaraH A. SMITH1 1 Australian Museum Research Institute, Australian Museum, 1 William Street, Sydney NSW 2010, Australia 2 Department of Biology, Villanova University, 800 Lancaster Avenue, Villanova, Pennsylvania 19085, United States of America 3 Faculty of Veterinary Science B01, University of Sydney NSW 2006, Australia ABSTRACT. Recent genetic studies have identified the New Caledonian scincid genus Lioscincus to be polyphyletic, comprising four distinct evolutionary lineages which we recognize at the generic level. The revised concept of Lioscincus s.s. now includes only the type species Lioscincus steindachneri Bocage, 1873 and the recently described Lioscincus vivae Sadlier, Bauer, Whitaker & Smith, 2004. The three remaining lineages identified are:Leiolopisma tillieri Ineich & Sadlier, 1991 and Lioscincus maruia Sadlier, Whitaker & Bauer, 1998 for which the genus Phasmasaurus gen. nov. is proposed; Lygosoma (Mocoa) nigrofasciolatus Peters, 1869 and Leiolopisma greeri Böhme, 1979 for which the genus Epibator gen. nov. is proposed; and Lygosoma (Leiolopisma) novaecaledoniae Parker, 1926 for which the genus Caesoris gen. nov. is proposed. Each of these genera is diagnosed by a suite of morphological apomorphies which in combination is unique within the Eugongylus group of skinks of which each is a member. -
The Mystery of the Lesser Stag Beetle Dorcus Parallelipipedus (L.) (Coleoptera: Lucanidae) Mycangium Yeasts by Masahiko Tanahashi 1 and Maria Fremlin *2
146 Bulletin of the Amateur Entomologists' Society The mystery of the lesser stag beetle Dorcus parallelipipedus (L.) (Coleoptera: Lucanidae) mycangium yeasts by Masahiko Tanahashi 1 and Maria Fremlin *2 1 National Institute of Advanced Industrial Science and Technology (AIST) Central 6, Tsukuba, Ibaraki 305-8566, J apan 2 25 Ireton Rd, Colch ester, Essex, CO3 3AT, UK - E-mail: [email protected] (Correspondence) Introduction The mycangium is a microbe-storage organ present in several wood-feeding invertebrates; for example, it has been known for some time that bark and ambrosia beetles, and even leaf-roller weevils carry symbiotic fungi in special structures on their bodies (Beaver, 1989; Kobayashi et al , 2008). However, this organ has only been discovered recently in stag beetles (Tanahashi et al. , 2010) and in a certain lizard beetle ( Toki et al ., 2012 ), probably because it is not an external structure. In their case, the mycangium is an ovipositor- associated organ, that is, an exoskeletal organ normally folded and hidden under the last tergal plate of the female’s abdomen. Remarkably, this organ is clearly represented, albeit without a description, in Franciscolo’s drawings of the dorsal view of the female reproductive system for a couple of Lucanidae species: Lucanus cervus and L. tetraodon (1997). However, he opted for ventral views of all the other species, including Dorcus parallelipipedus , in which case the mycangium is obscured by the reproductive organs. Since the author is no longer alive and the book is currently out of print, we reproduce below one of his diagrams with the mycangium marked by us (Figure 1).