An Annotated Checklist of the Coleoptera of the Smithsonian Environmental Research Center: the Scarabaeoidea
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Cravens Peak Scientific Study Report
Geography Monograph Series No. 13 Cravens Peak Scientific Study Report The Royal Geographical Society of Queensland Inc. Brisbane, 2009 The Royal Geographical Society of Queensland Inc. is a non-profit organization that promotes the study of Geography within educational, scientific, professional, commercial and broader general communities. Since its establishment in 1885, the Society has taken the lead in geo- graphical education, exploration and research in Queensland. Published by: The Royal Geographical Society of Queensland Inc. 237 Milton Road, Milton QLD 4064, Australia Phone: (07) 3368 2066; Fax: (07) 33671011 Email: [email protected] Website: www.rgsq.org.au ISBN 978 0 949286 16 8 ISSN 1037 7158 © 2009 Desktop Publishing: Kevin Long, Page People Pty Ltd (www.pagepeople.com.au) Printing: Snap Printing Milton (www.milton.snapprinting.com.au) Cover: Pemberton Design (www.pembertondesign.com.au) Cover photo: Cravens Peak. Photographer: Nick Rains 2007 State map and Topographic Map provided by: Richard MacNeill, Spatial Information Coordinator, Bush Heritage Australia (www.bushheritage.org.au) Other Titles in the Geography Monograph Series: No 1. Technology Education and Geography in Australia Higher Education No 2. Geography in Society: a Case for Geography in Australian Society No 3. Cape York Peninsula Scientific Study Report No 4. Musselbrook Reserve Scientific Study Report No 5. A Continent for a Nation; and, Dividing Societies No 6. Herald Cays Scientific Study Report No 7. Braving the Bull of Heaven; and, Societal Benefits from Seasonal Climate Forecasting No 8. Antarctica: a Conducted Tour from Ancient to Modern; and, Undara: the Longest Known Young Lava Flow No 9. White Mountains Scientific Study Report No 10. -
An Annotated Checklist of Wisconsin Scarabaeoidea (Coleoptera)
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida March 2002 An annotated checklist of Wisconsin Scarabaeoidea (Coleoptera) Nadine A. Kriska University of Wisconsin-Madison, Madison, WI Daniel K. Young University of Wisconsin-Madison, Madison, WI Follow this and additional works at: https://digitalcommons.unl.edu/insectamundi Part of the Entomology Commons Kriska, Nadine A. and Young, Daniel K., "An annotated checklist of Wisconsin Scarabaeoidea (Coleoptera)" (2002). Insecta Mundi. 537. https://digitalcommons.unl.edu/insectamundi/537 This Article is brought to you for free and open access by the Center for Systematic Entomology, Gainesville, Florida at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Insecta Mundi by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. INSECTA MUNDI, Vol. 16, No. 1-3, March-September, 2002 3 1 An annotated checklist of Wisconsin Scarabaeoidea (Coleoptera) Nadine L. Kriska and Daniel K. Young Department of Entomology 445 Russell Labs University of Wisconsin-Madison Madison, WI 53706 Abstract. A survey of Wisconsin Scarabaeoidea (Coleoptera) conducted from literature searches, collection inventories, and three years of field work (1997-1999), yielded 177 species representing nine families, two of which, Ochodaeidae and Ceratocanthidae, represent new state family records. Fifty-six species (32% of the Wisconsin fauna) represent new state species records, having not previously been recorded from the state. Literature and collection distributional records suggest the potential for at least 33 additional species to occur in Wisconsin. Introduction however, most of Wisconsin's scarabaeoid species diversity, life histories, and distributions were vir- The superfamily Scarabaeoidea is a large, di- tually unknown. -
Coleoptera: Scarabaeidae: Dynastinae: Oryctini) of the Neotropical and Nearctic Realms
Zootaxa 3090: 21–40 (2011) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2011 · Magnolia Press ISSN 1175-5334 (online edition) An annotated checklist of the oryctine rhinoceros beetles (Coleoptera: Scarabaeidae: Dynastinae: Oryctini) of the Neotropical and Nearctic realms HÉCTOR JAIME GASCA-ÁLVAREZ1 & BRETT C. RATCLIFFE2 1Corporación Sentido Natural, Carrera 70 H # 122 – 98. Int. 1, Bogotá, COLOMBIA. E-mail: [email protected] 2University of Nebraska State Museum, W436 Nebraska Hall, Lincoln, NE 68588-0514, USA. E-mail: [email protected] Abstract A brief review of the taxonomy and natural history of the New World Oryctini is provided. An updated and annotated checklist of the Oryctini of the Neotropical and Nearctic realms is included. This now includes 14 genera, 133 extant spe- cies, and two extinct species. Tehuacania porioni Dechambre, 2009 (Oryctini) is reduced to synonymy with Barutus hart- manni Ratcliffe, 2003 (Pentodontini). Key words: species catalog Introduction The tribe Oryctini is one of the most species rich groups of Dynastinae, and more than half the species occur in the Neotropical and Nearctic regions where there is considerable endemism (Mizinuma 1999). Species of Oryctini are characterized by mostly brown to black coloration (rarely pale yellow); a large, robust, elongate body; clypeus emarginate, acuminate, or with two teeth; mentum narrow; mandibles exposed and broad; antenna with 9–10 antennomeres, the club short or prolonged; protibia tridentate or quadridentate; prosternal process either long or short; elytra smooth, densely punctate, or with striae or rows of punctures; apex of metatibia usually with teeth, sometimes with lobes or crenulations; and coxal cavities broad. -
Taxonomie Und Verbreitung Von Valgus Hemipterus (Linnaeus, 1758) (Insecta: Coleoptera: Scarabaeidae: Cetoniinae: Valgini) 197-219 VERNATE 33/2014 S
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Veröffentlichungen des Naturkundemuseums Erfurt (in Folge VERNATE) Jahr/Year: 2014 Band/Volume: 33 Autor(en)/Author(s): Rössner Eckehard Artikel/Article: Taxonomie und Verbreitung von Valgus hemipterus (Linnaeus, 1758) (Insecta: Coleoptera: Scarabaeidae: Cetoniinae: Valgini) 197-219 VERNATE 33/2014 S. 197-219 Taxonomie und Verbreitung von Valgus hemipterus (Linnaeus, 1758) (Insecta: Coleoptera: Scarabaeidae: Cetoniinae: Valgini) ECKEHARD RÖSSNER Zusammenfassung Einleitung Bei der Untersuchung umfangreichen Materials von Der im deutschsprachigen Raum als Stolperkäfer oder Valgus hemipterus (Linnaeus, 1758) aus dem gesam- Bohrscharrkäfer bezeichnete Valgus hemipterus (Lin- ten bis heute bekannt gewordenen Verbreitungsgebiet naeus, 1758) gehört zu den Rosenkäfern im weiteren stellte sich heraus, dass die Art in zwei Unterarten auf- Sinne (Unterfamilie Cetoniinae) und ist im paläarkti- gespalten werden muss. Valgus hemipterus meridiona- schen Faunengebiet die populärste Art des Tribus Val- lis n. ssp. unterscheidet sich von der nominotypischen gini. Dies liegt an der weiten Verbreitung der Art, die Unterart vor allem im männlichen Genital. Die Unterart fast ganz Europa einschließt, an der relativ hohen Fund- kommt im Iran (Zagros- und Elburs-Gebirge), in der häufigkeit, und nicht zuletzt an ihrem etwas skurrilen Süd-Türkei (Taurus-Gebirge) und in der Levante (Sy- Aussehen. Die Oberseite des Käfers ist beschuppt, das rien, Libanon, Israel) vor und erreicht Höhenlagen bis Pronotum sehr uneben und die Elytren lassen Propygi- 2300 m. Dabei sind die Unterschiede in der externen dium und Pygidium frei. Hinzu kommt ein auffallen- Morphologie zwischen Populationen der neuen Unter- der Geschlechtsdimorphismus: Das Weibchen besitzt art aus dem Iran und denen der nominotypische Unter- einen Legestachel, der fast ein Fünftel der gesamten art besonders deutlich. -
The Beetle Fauna of Dominica, Lesser Antilles (Insecta: Coleoptera): Diversity and Distribution
INSECTA MUNDI, Vol. 20, No. 3-4, September-December, 2006 165 The beetle fauna of Dominica, Lesser Antilles (Insecta: Coleoptera): Diversity and distribution Stewart B. Peck Department of Biology, Carleton University, 1125 Colonel By Drive, Ottawa, Ontario K1S 5B6, Canada stewart_peck@carleton. ca Abstract. The beetle fauna of the island of Dominica is summarized. It is presently known to contain 269 genera, and 361 species (in 42 families), of which 347 are named at a species level. Of these, 62 species are endemic to the island. The other naturally occurring species number 262, and another 23 species are of such wide distribution that they have probably been accidentally introduced and distributed, at least in part, by human activities. Undoubtedly, the actual numbers of species on Dominica are many times higher than now reported. This highlights the poor level of knowledge of the beetles of Dominica and the Lesser Antilles in general. Of the species known to occur elsewhere, the largest numbers are shared with neighboring Guadeloupe (201), and then with South America (126), Puerto Rico (113), Cuba (107), and Mexico-Central America (108). The Antillean island chain probably represents the main avenue of natural overwater dispersal via intermediate stepping-stone islands. The distributional patterns of the species shared with Dominica and elsewhere in the Caribbean suggest stages in a dynamic taxon cycle of species origin, range expansion, distribution contraction, and re-speciation. Introduction windward (eastern) side (with an average of 250 mm of rain annually). Rainfall is heavy and varies season- The islands of the West Indies are increasingly ally, with the dry season from mid-January to mid- recognized as a hotspot for species biodiversity June and the rainy season from mid-June to mid- (Myers et al. -
South Carolina Department of Natural Resources
FOREWORD Abundant fish and wildlife, unbroken coastal vistas, miles of scenic rivers, swamps and mountains open to exploration, and well-tended forests and fields…these resources enhance the quality of life that makes South Carolina a place people want to call home. We know our state’s natural resources are a primary reason that individuals and businesses choose to locate here. They are drawn to the high quality natural resources that South Carolinians love and appreciate. The quality of our state’s natural resources is no accident. It is the result of hard work and sound stewardship on the part of many citizens and agencies. The 20th century brought many changes to South Carolina; some of these changes had devastating results to the land. However, people rose to the challenge of restoring our resources. Over the past several decades, deer, wood duck and wild turkey populations have been restored, striped bass populations have recovered, the bald eagle has returned and more than half a million acres of wildlife habitat has been conserved. We in South Carolina are particularly proud of our accomplishments as we prepare to celebrate, in 2006, the 100th anniversary of game and fish law enforcement and management by the state of South Carolina. Since its inception, the South Carolina Department of Natural Resources (SCDNR) has undergone several reorganizations and name changes; however, more has changed in this state than the department’s name. According to the US Census Bureau, the South Carolina’s population has almost doubled since 1950 and the majority of our citizens now live in urban areas. -
Quick Guide for the Identification Of
Quick Guide for the Identification of Maryland Scarabaeoidea Mallory Hagadorn Dr. Dana L. Price Department of Biological Sciences Salisbury University This document is a pictorial reference of Maryland Scarabaeoidea genera (and sometimes species) that was created to expedite the identification of Maryland Scarabs. Our current understanding of Maryland Scarabs comes from “An Annotated Checklist of the Scarabaeoidea (Coleoptera) of Maryland” (Staines 1984). Staines reported 266 species and subspecies using literature and review of several Maryland Museums. Dr. Price and her research students are currently conducting a bioinventory of Maryland Scarabs that will be used to create a “Taxonomic Guide to the Scarabaeoidea of Maryland”. This will include dichotomous keys to family and species based on historical reports and collections from all 23 counties in Maryland. This document should be cited as: Hagadorn, M.A. and D.L. Price. 2012. Quick Guide for the Identification of Maryland Scarabaeoidea. Salisbury University. Pp. 54. Questions regarding this document should be sent to: Dr. Dana L. Price - [email protected] **All pictures within are linked to their copyright holder. Table of Contents Families of Scarabaeoidea of Maryland……………………………………... 6 Geotrupidae……………………………………………………………………. 7 Subfamily Bolboceratinae……………………………………………… 7 Genus Bolbocerosoma………………………………………… 7 Genus Eucanthus………………………………………………. 7 Subfamily Geotrupinae………………………………………………… 8 Genus Geotrupes………………………………………………. 8 Genus Odonteus...……………………………………………… 9 Glaphyridae.............................................................................................. -
Dimensional Limits for Arthropod Eyes with Superposition Optics
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Vision Research 44 (2004) 2213–2223 www.elsevier.com/locate/visres Dimensional limits for arthropod eyes with superposition optics Victor Benno Meyer-Rochow a,*,Jozsef Gal b a School of Engineering and Sciences, International University Bremen (IUB), Campus Ring 6, Research II, D-28759 Bremen, Germany b Institute of Plant Biology, Biological Research Centre, Hungarian Academy of Sciences, Temesvari krt. 62, H-6701 Szeged, Hungary Received 10 December 2003; received in revised form 16 April 2004 Abstract An essential feature of the superposition type of compound eye is the presence of a wide zone, which is transparent and devoid of pigment and interposed between the distal array of dioptric elements and the proximally placed photoreceptive layer. Parallel rays, collected by many lenses, must (through reflection or refraction) cross this transparent clear-zone in such a way that they become focused on one receptor. Superposition depends mostly on diameter and curvature of the cornea, size and shape of the crystalline cone, lens cylinder properties of cornea and cone, dimensions of the receptor cells, and width of the clear-zone. We examined the role of the latter by geometrical, geometric-optical, and anatomical measurements and concluded that a minimal size exists, below which effective superposition can no longer occur. For an eye of a given size, it is not possible to increase the width of the clear-zone cz ¼ dcz=R1 and decrease R2 (i.e., the radius of curvature of the distal retinal surface) and/or c ¼ dc=R1 without reaching a limit. -
Phylogenetic Analysis of Geotrupidae (Coleoptera, Scarabaeoidea) Based on Larvae
Systematic Entomology (2004) 29, 509–523 Phylogenetic analysis of Geotrupidae (Coleoptera, Scarabaeoidea) based on larvae JOSE´ R. VERDU´ 1 , EDUARDO GALANTE1 , JEAN-PIERRE LUMARET2 andFRANCISCO J. CABRERO-SAN˜ UDO3 1Centro Iberoamericano de la Biodiversidad (CIBIO), Universidad de Alicante, Spain; 2CEFE, UMR 5175, De´ partement Ecologie des Arthropodes, Universite´ Paul Vale´ ry, Montpellier, France; and 3Departamento Biodiversidad y Biologı´ a Evolutiva, Museo Nacional de Ciencias Naturales (CSIC), Madrid, Spain Abstract. Thirty-eight characters derived from the larvae of Geotrupidae (Scarabaeoidea, Coleoptera) were analysed using parsimony and Bayesian infer- ence. Trees were rooted with two Trogidae species and one species of Pleocomidae as outgroups. The monophyly of Geotrupidae (including Bolboceratinae) is supported by four autapomorphies: abdominal segments 3–7 with two dorsal annulets, chaetoparia and acanthoparia of the epipharynx not prominent, glossa and hypopharynx fused and without sclerome, trochanter and femur without fossorial setae. Bolboceratinae showed notable differences with Pleocomidae, being more related to Geotrupinae than to other groups. Odonteus species (Bolboceratinae s.str.) appear to constitute the closest sister group to Geotrupi- nae. Polyphyly of Bolboceratinae is implied by the following apomorphic char- acters observed in the ‘Odonteus lineage’: anterior and posterior epitormae of epipharynx developed, tormae of epipharynx fused, oncyli of hypopharynx devel- oped, tarsal claws reduced or absent, plectrum and pars stridens of legs well developed and apex of antennal segment 2 with a unique sensorium. A ‘Bolbelas- mus lineage’ is supported by the autapomorphic presence of various sensoria on the apex of the antennal segment, and the subtriangular labrum (except Eucanthus). This group constituted by Bolbelasmus, Bolbocerosoma and Eucanthus is the first evidence for a close relationship among genera, but more characters should be analysed to test the support for the clade. -
Reproductive Behaviour and Development of the Dung Beetle Typhaeus Typhoeus (Coleoptera, Geotrupidae)
REPRODUCTIVE BEHAVIOUR AND DEVELOPMENT OF THE DUNG BEETLE TYPHAEUS TYPHOEUS (COLEOPTERA, GEOTRUPIDAE) by LIJBERTBRUSSAARD Dept. of Animal Ecology and Dept. of Soil Science & Geology, Agricultural University, Wageningen, The Netherlands . ABSTRACT This paper is part of a study of the contribution of dung beetles to soil formation in sandy soils. Typhaeus typhoeus (Linnaeus) has been selected because it makes deep burrows and is locally abundant. The beetles are active from autumn until spring, reproduction takes place from February to April. Sex pheromones probably influence pair formation. The sexes co operate in excavating a burrow (up to 0.7 m below surface) and in provisioning the burrow with dung as food for the larvae. Co-operation is reset by scraping each other across the thorax or elytra. Dung sausages, appr. 12.5 cm long and 15 mm in diameter, are manufac tured above each other. Development is rapid at 13—17°C. The life cycle is accelerated by a cold period in the third larval stage. These requirements are met by soil temperatures up to 15° C in summer and down to 5 °C in winter. The life cycle lasts two years, but longer under certain conditions. Newly hatched beetles make their way to the surface through the soil, but do not follow the old shaft. Adults reproduce only once. Differential rate of com pletion of the life cycle and occasional flying probably reduce the risk of local extinction. The study is thought to be relevant for behavioural ecology and soil science. CONTENTS tion of how much dung beetles contribute to Introduction 203 soil formation today. -
Evolutionary Patterns of Asymmetric Genitalia in the Beetle Tribe Cyclocephalini (Coleoptera: Scarabaeidae: Dynastinae)
Contributions to Zoology, 82 (2) 95-106 (2013) Evolutionary patterns of asymmetric genitalia in the beetle tribe Cyclocephalini (Coleoptera: Scarabaeidae: Dynastinae) Thijmen Breeschoten1, 2, 4, Daniel R. Clark3, Menno Schilthuizen1, 2 1 Character Evolution Group, Naturalis Biodiversity Center, Darwinweg 2, 2333 CR Leiden, The Netherlands 2 Institute Biology Leiden, Leiden University, Sylviusweg 72, 2333 BE Leiden, The Netherlands 3 Department of Biological Sciences, 537 Hubbard Hall, Wichita State University, Wichita, Kansas, 68588-0514, USA 4 E-mail: [email protected] Key words: chirality, left-right asymmetry, micro-CT scanning, morphometrics, Procrustes distance Abstract Currently, several chief mechanisms are recognized as potentially being responsible for this vast diversity The evolution of asymmetric genitalia is a common and recurrent (Schilthuizen, 2003; Eberhard, 2010). First, sexual selec- phenomenon in a wide variety of insect taxa. However, little is tion by cryptic female choice may drive the evolution understood about the evolution of left-right asymmetry in repro- ductive structures. Since a better knowledge of it could have an of exaggerated structures on male genitalia (Eberhard, important impact on the study of genital evolution, in the present 1985). Second, sperm competition, the post-copulatory study we investigate the phylogenetic and evolutionary patterns sexual selection between males inside the females’ re- of asymmetric male genitalia in Cyclocephalini. We use a Pro- productive tract is possibly important in creating the crustes distance based method for quantifying asymmetry. Analysis of 119 species belonging to 14 genera revealed a diverse diversity in male genital morphology (Parker, 1970). array of asymmetries with a strong indication that asymmetries This mechanism appears to be involved in, for example, are more strongly developed in the terminal part of the aedeagus. -
Review of Literature and the Biology of the Australian Ceratocanthidae (Insecta: Coleoptera) by Dr Trevor J
Calodema Volume 7 (2006) Review of literature and the biology of the Australian Ceratocanthidae (Insecta: Coleoptera) by Dr Trevor J. Hawkeswood* *PO Box 842, Richmond, New South Wales, 2753, Australia (www.calodema.com) Hawkeswood, T.J. (2006). Review of literature and the biology of the Australian Ceratocanthidae (Insecta: Coleoptera). Calodema, 7: 8-11. Abstract: The literature pertaining to the Australian Ceratocanthidae (Coleoptera) is reviewed. The information available indicates that very little is known about the three Australian species, all of which occur in Queensland. Introduction The family Ceratocanthidae ( = Acanthoceridae) is found in the tropics and subtropics of the world and is represented by about 40 genera and 320 species (Ballerio, 2000; Howden & Gill, 2000; Grebennikov et al., 2002) but this number is likely to rise in the coming years as a result of undescribed species being discovered (Grebennikov et al., 2002). The Ceratocanthidae exhibit a pantropical distribution, with few species living in the temperate regions of the Americas, South Africa and south-east Asia (Grebennikov et al., 2002). Taxonomically, it is widely considered as a separate family of the superfamily Scarabaeoidea and appears to be more closely related to the Hybosoridae and Ochodaeidae (Lawrence & Newton, 1982; Browne & Scholtz, 1999; Grebennikov et al., 2002, 2004; Grebennikov & Scholtz, 2004) and the Trogidae (Crowson, 1955). Ceratocanthid beetles are characterised by having a strongly convex body which allows the mouth-parts, abdomen and parts of the legs to be completely concealed when they roll themselves into a pill-shaped form or little compact ball, hence the common name of pill scarab beetle or ball beetle for the group.