Common Names for Australian Ants (Hymenoptera: Formicidae)
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Appreciably Modified
VI1.-KEYS TO THE GESER.1 AND SUBGEKERA OF ASTS BY WM. 31. WHEELER KEYTO THE SUBFAMILIES~ 8, 0 1. Cloacal orifice round, tefminal, surrounded by a fringe of hairs; sting transformed into a sustentacular apparatus for the orifice of the poison vesicle, which has a peculiar structure called by Fore1 '' pulviniferous vesicle" (vessie 2 coussinet) . Abdominal pedicel consisting of a single segment; no constriction between the second and third segments. Male genitalia not retractile. Nymphs rarely naked, most frequently enclosed in a cocoon. FORMICINA3. Cloacal orifice in the shape of a slit. ........................ .2. 2. Sting rudimentary (except Aneuretus) ; abdominal pedicel con- sisting of a single segment; no constriction between the second and third segments of the abdomen; the poison glands are often vestigial and there are anal glands which secrete an aromatic product of characteristic odor (Tapinoma-odor). Nymphs without a cocoon. ..........DOLICHODERINAE. Sting developed, though sometimes very small, but capable never- theless of being exserted from the abdomen. The first two segments of the abdomen usually modified, either forming together a two-jointed pedicel, or the first alone (petiole) forming the pedicel, the second (postpetiole) being merely constricted posteriorly and articulating with a spheroidal surface of the third segment, which is usually transversely striated (stridulatory organ) ; rarely the second segment is not appreciably modified. .................................... .3. 3. Pedicel of two segments, the petiole and the postpetiole; rarely (in Melissotarsus, e. 9.) the postpetiole is attached to the follow- ing segment over its whole extent. Frontal carin= usually separated from each other (except in the Melissotarsini and certain Attini). In the male the copulatory organs are almost always exserted (being entirely retractile in certain genera of the Solenopsidini only) ; cerci nearly always present (except Anergates) . -
Winged Ants (Hymenoptera: Formicidae) Presence in Twigs on the Leaf Litter of Atlantic Forest
Biota Neotropica 19(3): e20180694, 2019 www.scielo.br/bn ISSN 1676-0611 (online edition) Inventory Winged ants (Hymenoptera: Formicidae) presence in twigs on the leaf litter of Atlantic Forest Tae Tanaami Fernandes1 , Rogério R. Silva2, Débora Rodrigues de Souza-Campana2, Otávio Guilherme Morais da Silva2 & Maria Santina de Castro Morini1* 1Universidade de Mogi das Cruzes, Laboratório de Mirmecologia do Alto Tietê, Rua Dr. Cândido Xavier de Almeida e Souza, 200, CEP 08780-911, Mogi das Cruzes, SP, Brasil 2Museu Paraense Emílio Goeldi, Coordenação de Ciências da Terra e Ecologia, Avenida Perimetral, 1901, Terra Firme, CEP 66077-830, Belém, PA, Brasil *Corresponding author: Maria Santina de Castro Morini, e-mail: [email protected] FERNANDES, T. T., SILVA, R. R., SOUZA-CAMPANA, D. R., SILVA, O. G. M., MORINI, M. S. C. Winged ants (Hymenoptera: Formicidae) presence in twigs on the leaf litter of Atlantic Forest. Biota Neotropica 19(3): e20180694. http://dx.doi.org/10.1590/1676-0611-BN-2018-0694 Abstract: In the leaf litter, ants have various nesting resources available, such as live or dead trunks, twigs, leaves, fruits and seeds. On the twigs, there are adults and immature individuals, but also the queen and winged. The production of wings requires time and energy from the colony. The objective of this study was to investigate the presence of winged in ant colonies in twigs on the leaf litter. Our prediction is that the richness and abundance of winged in twigs are the greatest in rainy months. We collected all twigs with ants in 552 plots with 16 m2, totaling 8,832 m2 of leaf litter, in areas located in the Brazilian Atlantic Domain. -
Ant Type Specimens (Hymenoptera, Formicidae) Deposited in the Museu De Zoologia Da Universidade De São Paulo, Brazil
Volume 48(11):75-88, 2008 Catalogue of “poneromorph” ant type specimens (Hymenoptera, Formicidae) deposited in the Museu de Zoologia da Universidade de São Paulo, Brazil Cristiane P. Scott-Santos Flávia A. Esteves Carlos Roberto F. Brandão AbsTracT The present catalogue lists the type specimes of 112 nominal “poneromorph” ant species housed in the Formicidae collection of the Hymenoptera laboratory, Museu de Zoologia da Universidade de São Paulo (MZSP). The catalogue includes types of Amblyoponinae, Ectatomminae, Heteroponerinae, Ponerinae, and Proceratiinae, that is, all poneromorph (sensu Bolton, 2003) but for the monotypic Paraponerinae, of which the collection bears no type specimens. We present here information on type categories (holotype, paratype, syntype, lectotype, and paralectotype), label data, nomenclatural changes since the original description and type specimens conservation status. At last we present indexes for the taxa names presented. Keywords: Hymenoptera, ants, types, MZSP, Amblyoponinae, Ectatomminae, Heteroponerinae, Ponerinae, Proceratiinae. INTRODucTION The purpose of the present catalogue is to pro- vide updated information on poneromorph type The Formicidae collection housed in the Hy- specimes of the MZSP collection, following Article menoptera laboratory of the Museu de Zoologia da 72 F.4 of the International Code for Zoological No- Universidade de São Paulo (MZSP) is under con- menclature (1999). struction since the end of the 19th century and is to- The poneromorph group of ants, as defined by day one of the largest and more representative ant col- Bolton (2003), is distributed worldwide and consists lections in and for the Neotropical region, as regard of circa 1,700 described species in 49 genera of six to the number of specimens, including types, and subfamilies: Amblyoponinae, Ectatomminae, Hetero- localities (Brandão, 2000). -
Wildlife Trade Operation Proposal – Queen of Ants
Wildlife Trade Operation Proposal – Queen of Ants 1. Title and Introduction 1.1/1.2 Scientific and Common Names Please refer to Attachment A, outlining the ant species subject to harvest and the expected annual harvest quota, which will not be exceeded. 1.3 Location of harvest Harvest will be conducted on privately owned land, non-protected public spaces such as footpaths, roads and parks in Victoria and from other approved Wildlife Trade Operations. Taxa not found in Victoria will be legally sourced from other approved WTOs or collected by Queen of Ants’ representatives from unprotected areas. This may include public spaces such as roadsides and unprotected council parks, and other property privately owned by the representatives. 1.4 Description of what is being harvested Please refer to Attachment A for an outline of the taxa to be harvested. The harvest is of live adult queen ants which are newly mated. 1.5 Is the species protected under State or Federal legislation Ants are non-listed invertebrates and are as such unprotected under Victorian and other State Legislation. Under Federal legislation the only protection to these species relates to the export of native wildlife, which this application seeks to satisfy. No species listed under the EPBC Act as threatened (excluding the conservation dependent category) or listed as endangered, vulnerable or least concern under Victorian legislation will be harvested. 2. Statement of general goal/aims The applicant has recently begun trading queen ants throughout Victoria as a personal hobby and has received strong overseas interest for the species of ants found. -
Differences in the Sugar Composition of the Honeydew of Polyphagous
NOTE Eur. J. Entomol. 108: 705–709, 2011 http://www.eje.cz/scripts/viewabstract.php?abstract=1671 ISSN 1210-5759 (print), 1802-8829 (online) Differences in the sugar composition of the honeydew of polyphagous brown soft scale Coccus hesperidum (Hemiptera: Sternorrhyncha: Coccoidea) feeding on various host plants KATARZYNA GOLAN 1 and AGNIESZKA NAJDA2 1Department of Entomology, University of Life Sciences in Lublin, LeszczyĔskiego 7, 20-069 Lublin, Poland; e-mail: [email protected] 2 Department of Vegetable and Medicinal Plants, University of Life Sciences in Lublin, LeszczyĔskiego 58, 20-068 Lublin, Poland Key words. Coccoidea, Coccus hesperidum, brown scale insects, honeydew, host plants, soft scale, sugar composition Abstract. Plant chemical composition is an important determinant of host plant-insect interactions. For many insects sugars are the main factors determining the acceptability of a plant. This study investigated changes in plant chemical composition and differences in sugar composition of different host plants induced by the feeding of Coccus hesperidum L. (Hemiptera: Sternorrhyncha: Coccoi- dea). Present in plant extracts and honeydew there were three monosaccharide sugars: glucose, fructose and arabinose, and one disaccharide – sucrose. Arabinose was only found in extracts of Ficus benjamina plants. The sugar content of the honeydew was greater than in the extracts of control plants and lower than that in the extracts of infested plants. The honeydew collected from C. hesperidum feeding on the three plant species differed significantly in sugar content. Extracts of coccid infested plants of the three species used in this study contained more sugar than the un-infested control plants. The results show that honeydew composition of scale insects differ and the differences reflect the chemical composition of the host plants. -
Level 1 Fauna Survey of the Gruyere Gold Project Borefields (Harewood 2016)
GOLD ROAD RESOURCES LIMITED GRUYERE PROJECT EPA REFERRAL SUPPORTING DOCUMENT APPENDIX 5: LEVEL 1 FAUNA SURVEY OF THE GRUYERE GOLD PROJECT BOREFIELDS (HAREWOOD 2016) Gruyere EPA Ref Support Doc Final Rev 1.docx Fauna Assessment (Level 1) Gruyere Borefield Project Gold Road Resources Limited January 2016 Version 3 On behalf of: Gold Road Resources Limited C/- Botanica Consulting PO Box 2027 BOULDER WA 6432 T: 08 9093 0024 F: 08 9093 1381 Prepared by: Greg Harewood Zoologist PO Box 755 BUNBURY WA 6231 M: 0402 141 197 T/F: (08) 9725 0982 E: [email protected] GRUYERE BOREFIELD PROJECT –– GOLD ROAD RESOURCES LTD – FAUNA ASSESSMENT (L1) – JAN 2016 – V3 TABLE OF CONTENTS SUMMARY 1. INTRODUCTION .....................................................................................................1 2. SCOPE OF WORKS ...............................................................................................1 3. RELEVANT LEGISTALATION ................................................................................2 4. METHODS...............................................................................................................3 4.1 POTENTIAL VETEBRATE FAUNA INVENTORY - DESKTOP SURVEY ............. 3 4.1.1 Database Searches.......................................................................................3 4.1.2 Previous Fauna Surveys in the Area ............................................................3 4.1.3 Existing Publications .....................................................................................5 4.1.4 Fauna -
Morphology of the Mandibular Gland of the Ant Paraponera Clavata (Hymenoptera: Paraponerinae)
Received: 9 October 2018 Revised: 17 January 2019 Accepted: 2 February 2019 DOI: 10.1002/jemt.23242 RESEARCH ARTICLE Morphology of the mandibular gland of the ant Paraponera clavata (Hymenoptera: Paraponerinae) Thito Thomston Andrade1 | Wagner Gonzaga Gonçalves2 | José Eduardo Serrão2 | Luiza Carla Barbosa Martins1 1Programa de Pós-Graduação em Biodiversidade, Ambiente e Saúde, Abstract Departamento de Biologia e Química, The ant Paraponera clavata (Fabricius, 1775) is the only extant species of Paraponerinae and is Universidade Estadual do Maranhão, Caxias, widely distributed in Brazilian forests. Aspects of its biology are documented extensively in the Maranhão, Brazil literature; however, knowledge of P. clavata internal morphology, specifically of exocrine glands, 2Departamento de Biologia Geral, Universidade Federal de Viçosa, Viçosa, is restricted to the venom apparatus. The objective of this study was to describe the mandibular Minas Gerais, Brazil gland morphology of P. clavata workers. The mandibular gland is composed of a reservoir con- nected to a cluster of Type III secretory cells with cytoplasm rich in mitochondria and lipid drop- Correspondence lets, similar to that of other ants. Notably, the glandular secretion is rich in protein and has a Luiza Carla Barbosa Martins, Programa de Pós- Graduação em Biodiversidade, Ambiente e solid aspect. This is the first morphological description of the mandibular gland of P. clavata. Saúde, Departamento de Biologia e Química, Universidade Estadual do Maranhão, Caxias, Research Highlights Maranhão, Brazil. This study presents the morphological description of the mandibular gland of Paraponera clavata Email: [email protected] (Hymenoptera: Paraponerinae). Singular characteristics of the gland are described: the glandular Review Editor: George Perry secretion is rich in protein and has a solid aspect. -
Hymenoptera: Formicidae)
Myrmecological News 20 25-36 Online Earlier, for print 2014 The evolution and functional morphology of trap-jaw ants (Hymenoptera: Formicidae) Fredrick J. LARABEE & Andrew V. SUAREZ Abstract We review the biology of trap-jaw ants whose highly specialized mandibles generate extreme speeds and forces for predation and defense. Trap-jaw ants are characterized by elongated, power-amplified mandibles and use a combination of latches and springs to generate some of the fastest animal movements ever recorded. Remarkably, trap jaws have evolved at least four times in three subfamilies of ants. In this review, we discuss what is currently known about the evolution, morphology, kinematics, and behavior of trap-jaw ants, with special attention to the similarities and key dif- ferences among the independent lineages. We also highlight gaps in our knowledge and provide suggestions for future research on this notable group of ants. Key words: Review, trap-jaw ants, functional morphology, biomechanics, Odontomachus, Anochetus, Myrmoteras, Dacetini. Myrmecol. News 20: 25-36 (online xxx 2014) ISSN 1994-4136 (print), ISSN 1997-3500 (online) Received 2 September 2013; revision received 17 December 2013; accepted 22 January 2014 Subject Editor: Herbert Zettel Fredrick J. Larabee (contact author), Department of Entomology, University of Illinois, Urbana-Champaign, 320 Morrill Hall, 505 S. Goodwin Ave., Urbana, IL 61801, USA; Department of Entomology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20013-7012, USA. E-mail: [email protected] Andrew V. Suarez, Department of Entomology and Program in Ecology, Evolution and Conservation Biology, Univer- sity of Illinois, Urbana-Champaign, 320 Morrill Hall, 505 S. -
Microsoft Photo Editor
Environmental research on the impact of bumblebees in Australia and facilitation of national communication for and against further introductions Kaye Hergstrom Tasmanian Museum & Art Gallery Project Number: VG99033 VG99033 This report is published by Horticulture Australia Ltd to pass on information concerning horticultural research and development undertaken for the vegetable industry. The research contained in this report was funded by Horticulture Australia Ltd with the financial support of the vegetable industry and Hydroponic Farmers Federation. All expressions of opinion are not to be regarded as expressing the opinion of Horticulture Australia Ltd or any authority of the Australian Government. The Company and the Australian Government accept no responsibility for any of the opinions or the accuracy of the information contained in this report and readers should rely upon their own enquiries in making decisions concerning their own interests. ISBN 0 7341 0532 0 Published and distributed by: Horticulture Australia Ltd Level 1 50 Carrington Street Sydney NSW 2000 Telephone: (02) 8295 2300 Fax: (02) 8295 2399 E-Mail: [email protected] © Copyright 2002 Environmental Research on the Impact of Bumblebees in Australia and Facilitation of National Communication for/against Further Introduction Prepared by Kaye Hergstrom1, Roger Buttermore1, Owen Seeman2 and Bruce McCorkell2 1Tasmanian Museum and Art Gallery, 40 Macquarie St, Hobart Tas., 2Department of Primary Industries, Water and the Environment, Tas. 13 St Johns Ave, New Town, Tas. Horticulture Australia Project No: VG99033 The authors gratefully acknowledge the funding support provided by: Horticulture Australia Additional support in kind has been provided by: The Tasmanian Museum and Art Gallery Front cover illustration by Mike Tobias; design by Lexi Clark Any recommendations contained in this publication do not necessarily represent current HRDC policy. -
Bushhopper Stalk-Eyed Fly Coconut Crab Periodical Cicada
PIOTR NASKRECKI PHOTO BANNERS HANGING IN CHANGING EXHIBIT GALLERY Bushhopper Stalk-Eyed Fly Phymateus viridipes Diasemopsis fasciata Gorongosa National Park, Mozambique Gorongosa National Park, Mozambique A nymph of the bushhopper from Mozambique Like antlers on a deer’s head, the long can afford to be slow and conspicuous thanks eyestalks on this fly’s head are used in maleto- to the toxins in its body. These insects feed male combat, allowing the individual with on plants rich in poisonous metabolites, the largest stalks to win access to females including some that can cause heart failure, so most predators avoid them. Coconut Crab Periodical Cicada Birgus latro Magicicada septendecim Guadalcanal, Solomon Islands Annandale, Virginia The coconut crab is not just another land Periodical cicadas spend seventeen years crab; it is the largest living terrestrial underground, feeding on the roots of plants. invertebrate, reaching a weight of nine After that time they all emerge at the same pounds and a leg span of over three feet. time, causing consternation in people and Their lifespan is equally impressive, and the a feeding frenzy in birds. A newly emerged largest individuals are believed to be forty to (eclosed) periodical cicada is almost snow sixty years old. white, but within a couple of hours its body darkens and the exoskeleton becomes hard. BIG BUGS • Dec. 31, 2015 - April 17, 2016 Virginia Living Museum • 524 J. Clyde Morris Blvd. • Newport News, VA 23601 • 757-595-1900 • thevlm.org PIOTR NASKRECKI PHOTO BANNERS HANGING IN CHANGING EXHIBIT GALLERY Dung Beetles Lappet Moth Kheper aegyptiorum Chrysopsyche lutulenta Gorongosa National Park, Mozambique Gorongosa National Park, Mozambique Dung beetles are very important members of At the beginning of the dry season in Savanna communities. -
Borowiec Et Al-2020 Ants – Phylogeny and Classification
A Ants: Phylogeny and 1758 when the Swedish botanist Carl von Linné Classification published the tenth edition of his catalog of all plant and animal species known at the time. Marek L. Borowiec1, Corrie S. Moreau2 and Among the approximately 4,200 animals that he Christian Rabeling3 included were 17 species of ants. The succeeding 1University of Idaho, Moscow, ID, USA two and a half centuries have seen tremendous 2Departments of Entomology and Ecology & progress in the theory and practice of biological Evolutionary Biology, Cornell University, Ithaca, classification. Here we provide a summary of the NY, USA current state of phylogenetic and systematic 3Social Insect Research Group, Arizona State research on the ants. University, Tempe, AZ, USA Ants Within the Hymenoptera Tree of Ants are the most ubiquitous and ecologically Life dominant insects on the face of our Earth. This is believed to be due in large part to the cooperation Ants belong to the order Hymenoptera, which also allowed by their sociality. At the time of writing, includes wasps and bees. ▶ Eusociality, or true about 13,500 ant species are described and sociality, evolved multiple times within the named, classified into 334 genera that make up order, with ants as by far the most widespread, 17 subfamilies (Fig. 1). This diversity makes the abundant, and species-rich lineage of eusocial ants the world’s by far the most speciose group of animals. Within the Hymenoptera, ants are part eusocial insects, but ants are not only diverse in of the ▶ Aculeata, the clade in which the ovipos- terms of numbers of species. -
Hymenoptera: Formicidae) Along an Elevational Gradient at Eungella in the Clarke Range, Central Queensland Coast, Australia
RAINFOREST ANTS (HYMENOPTERA: FORMICIDAE) ALONG AN ELEVATIONAL GRADIENT AT EUNGELLA IN THE CLARKE RANGE, CENTRAL QUEENSLAND COAST, AUSTRALIA BURWELL, C. J.1,2 & NAKAMURA, A.1,3 Here we provide a faunistic overview of the rainforest ant fauna of the Eungella region, located in the southern part of the Clarke Range in the Central Queensland Coast, Australia, based on systematic surveys spanning an elevational gradient from 200 to 1200 m asl. Ants were collected from a total of 34 sites located within bands of elevation of approximately 200, 400, 600, 800, 1000 and 1200 m asl. Surveys were conducted in March 2013 (20 sites), November 2013 and March–April 2014 (24 sites each), and ants were sampled using five methods: pitfall traps, leaf litter extracts, Malaise traps, spray- ing tree trunks with pyrethroid insecticide, and timed bouts of hand collecting during the day. In total we recorded 142 ant species (described species and morphospecies) from our systematic sampling and observed an additional species, the green tree ant Oecophylla smaragdina, at the lowest eleva- tions but not on our survey sites. With the caveat of less sampling intensity at the lowest and highest elevations, species richness peaked at 600 m asl (89 species), declined monotonically with increasing and decreasing elevation, and was lowest at 1200 m asl (33 spp.). Ant species composition progres- sively changed with increasing elevation, but there appeared to be two gradients of change, one from 200–600 m asl and another from 800 to 1200 m asl. Differences between the lowland and upland faunas may be driven in part by a greater representation of tropical and arboreal-nesting sp ecies in the lowlands and a greater representation of subtropical species in the highlands.