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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. -
Genus Myrmecocystus) Estimated from Mitochondrial DNA Sequences
MOLECULAR PHYLOGENETICS AND EVOLUTION Molecular Phylogenetics and Evolution 32 (2004) 416–421 www.elsevier.com/locate/ympev Short communication Phylogenetics of the new world honey ants (genus Myrmecocystus) estimated from mitochondrial DNA sequences D.J.C. Kronauer,* B. Holldobler,€ and J. Gadau University of Wu€rzburg, Institute of Behavioral Physiology and Sociobiology, Biozentrum, Am Hubland, 97074 Wu€rzburg, Germany Received 8 January 2004; revised 9 March 2004 Available online 6 May 2004 1. Introduction tes. The nominate subgenus contains all the light colored, strictly nocturnal species, the subgenus Eremnocystus Honey pot workers that store immense amounts of contains small, uniformly dark colored species, and the food in the crop and are nearly immobilized due to their subgenus Endiodioctes contains species with a ferrugi- highly expanded gasters are known from a variety of ant nous head and thorax and darker gaster. Snelling (1976) species in different parts of the world, presumably as proposed that the earliest division within the genus was adaptations to regular food scarcity in arid habitats that between the line leading to the subgenus Myrmec- (Holldobler€ and Wilson, 1990). Although these so called ocystus and that leading to Eremnocystus plus Endiodi- repletes are taxonomically fairly widespread, the phe- octes (maybe based on diurnal versus nocturnal habits) nomenon is most commonly associated with species of and that the second schism occurred when the Eremno- the New World honey ant genus Myrmecocystus, whose cystus line diverged from that of Endiodioctes. repletes have a long lasting reputation as a delicacy with Based on external morphology and data from both indigenous people. -
Hymenoptera: Formicidae: Formicinae)
Zootaxa 3669 (3): 287–301 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2013 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3669.3.5 http://zoobank.org/urn:lsid:zoobank.org:pub:46C8F244-E62F-4FC6-87DF-DEB8A695AB18 Revision of the Australian endemic ant genera Pseudonotoncus and Teratomyrmex (Hymenoptera: Formicidae: Formicinae) S.O. SHATTUCK1 & A.J. O’REILLY2 1CSIRO Ecosystem Sciences, GPO Box 1700, Canberra, ACT 2601, Australia. E-mail: [email protected] 2Centre for Tropical Biodiversity & Climate Change, School of Marine & Tropical Biology, James Cook University, Townsville, Queensland 4811 Abstract The Australian endemic formicine ant genera Pseudonotoncus and Teratomyrmex are revised and their distributions and biologies reviewed. Both genera are limited to forested areas along the east coast of Australia. Pseudonotoncus is known from two species, P. eurysikos (new species) and P. hirsutus (= P. turneri, new synonym), while Teratomyrmex is known from three species, T. greavesi, T. substrictus (new species) and T. tinae (new species). Distribution modelling was used to examine habitat preferences within the Pseudonotoncus species. Key words: Formicidae, Pseudonotoncus, Teratomyrmex, Australia, new species, key, MaxEnt Introduction Australia has a rich and diverse ant fauna, with over 1400 native species assigned to 100 genera. Of these 100 genera, 18 are endemic to Australia. These include Adlerzia, Anisopheidole, Austromorium, Doleromyrma, Epopostruma, Froggattella, Machomyrma, Mesostruma, Myrmecorhynchus, Nebothriomyrmex, Nothomyrmecia, Notostigma, Melophorus, Onychomyrma, Peronomyrmex, Pseudonotoncus, Stigmacros and Teratomyrmex. In the present study we revise two of these endemic genera, Pseudonotoncus and Teratomyrmex. Pseudonotoncus is found along the Australian east coast from the wet tropics in North Queensland to southern Victoria in rainforest and wet and dry sclerophyll forests. -
Formicidae: Catalogue of Family-Group Taxa
FORMICIDAE: CATALOGUE OF FAMILY-GROUP TAXA [Note (i): the standard suffixes of names in the family-group, -oidea for superfamily, –idae for family, -inae for subfamily, –ini for tribe, and –ina for subtribe, did not become standard until about 1905, or even much later in some instances. Forms of names used by authors before standardisation was adopted are given in square brackets […] following the appropriate reference.] [Note (ii): Brown, 1952g:10 (footnote), Brown, 1957i: 193, and Brown, 1976a: 71 (footnote), suggested the suffix –iti for names of subtribal rank. These were used only very rarely (e.g. in Brandão, 1991), and never gained general acceptance. The International Code of Zoological Nomenclature (ed. 4, 1999), now specifies the suffix –ina for subtribal names.] [Note (iii): initial entries for each of the family-group names are rendered with the most familiar standard suffix, not necessarily the original spelling; hence Acanthostichini, Cerapachyini, Cryptocerini, Leptogenyini, Odontomachini, etc., rather than Acanthostichii, Cerapachysii, Cryptoceridae, Leptogenysii, Odontomachidae, etc. The original spelling appears in bold on the next line, where the original description is cited.] ACANTHOMYOPSINI [junior synonym of Lasiini] Acanthomyopsini Donisthorpe, 1943f: 618. Type-genus: Acanthomyops Mayr, 1862: 699. Taxonomic history Acanthomyopsini as tribe of Formicinae: Donisthorpe, 1943f: 618; Donisthorpe, 1947c: 593; Donisthorpe, 1947d: 192; Donisthorpe, 1948d: 604; Donisthorpe, 1949c: 756; Donisthorpe, 1950e: 1063. Acanthomyopsini as junior synonym of Lasiini: Bolton, 1994: 50; Bolton, 1995b: 8; Bolton, 2003: 21, 94; Ward, Blaimer & Fisher, 2016: 347. ACANTHOSTICHINI [junior synonym of Dorylinae] Acanthostichii Emery, 1901a: 34. Type-genus: Acanthostichus Mayr, 1887: 549. Taxonomic history Acanthostichini as tribe of Dorylinae: Emery, 1901a: 34 [Dorylinae, group Cerapachinae, tribe Acanthostichii]; Emery, 1904a: 116 [Acanthostichii]; Smith, D.R. -
Hymenoptera, Formicidae) 1 Doi: 10.3897/Zookeys.700.11784 Research Article Launched to Accelerate Biodiversity Research
A peer-reviewed open-access journal ZooKeys 700: 1–420 (2017)Revision of the ant genus Melophorus (Hymenoptera, Formicidae) 1 doi: 10.3897/zookeys.700.11784 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Revision of the ant genus Melophorus (Hymenoptera, Formicidae) Brian E. Heterick1,2, Mark Castalanelli3, Steve O. Shattuck4 1 Curtin University of Technology, GPO Box U1987, Perth WA, Australia, 6845 2 Western Australian Museum, Locked Bag 49, Welshpool DC. WA, Australia, 6986 3 EcoDiagnostics Pty Ltd, 48 Banksia Rd, Welshpool WA 6106 4 C/o CSIRO Entomology, P. O. Box 1700, Canberra, Australia, ACT 2601 Corresponding author: Brian Heterick ([email protected]) Academic editor: B. Fisher | Received 17 January 2017 | Accepted 22 June 2017 | Published 20 September 2017 http://zoobank.org/EBA43227-20AD-4CFF-A04E-8D2542DDA3D6 Citation: Heterick BE, Castalanelli M, Shattuck SO (2017) Revision of the ant genus Melophorus (Hymenoptera, Formicidae). ZooKeys 700: 1–420. https://doi.org/10.3897/zookeys.700.11784 Abstract The fauna of the purely Australian formicine ant genus Melophorus (Hymenoptera: Formicidae) is revised. This project involved integrated morphological and molecular taxonomy using one mitochondrial gene (COI) and four nuclear genes (AA, H3, LR and Wg). Seven major clades were identified and are here designated as the M. aeneovirens, M. anderseni, M. biroi, M. fulvihirtus, M. ludius, M. majeri and M. potteri species-groups. Within these clades, smaller complexes of similar species were also identified and designated species-complexes. The M. ludius species-group was identified purely on molecular grounds, as the morphol- ogy of its members is indistinguishable from typical members of the M. -
Title: 1 Phylogeny, Evolution, and Classification of the Ant Genus
bioRxiv preprint doi: https://doi.org/10.1101/2021.07.14.452383; this version posted July 15, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 Title: 2 Phylogeny, evolution, and classification of the ant genus Lasius, the tribe Lasiini, and the 3 subfamily Formicinae (Hymenoptera: Formicidae) 4 5 Authors and affiliations: 6 B. E. Boudinot1,2, M. L. Borowiec1,3,4, M. M. Prebus1,5* 7 1Department of Entomology & Nematology, University of California, Davis CA 8 2Friedrich-Schiller-Universität Jena, Institut für Spezielle Zoologie, Jena, Germany 9 3Department of Plant Pathology, Entomology and Nematology, University of Idaho, Moscow ID 10 4Institute for Bioinformatics and Evolutionary Studies, University of Idaho, Moscow ID 11 5School of Life Sciences, Arizona State University, Tempe AZ 12 *Corresponding author. 13 14 Author ZooBank LSIDs: 15 Borowiec: http://zoobank.org/urn:lsid:zoobank.org:author:411B711F-605B-4C4B-ABDB- 16 D4D96075CE48 17 Boudinot: http://zoobank.org/urn:lsid:zoobank.org:author:919F03B0-60BA-4379-964D- 18 A56EB582E16D 19 Prebus: http://zoobank.org/urn:lsid:zoobank.org:author:1A6494C7-795E-455C-B66F- 20 7F6C32F76584 21 22 ZooBank Article LSID: http://zoobank.org/urn:lsid:zoobank.org:pub:016059BA-33C3-43B2- 23 ADAD-6807DC5CB6D8 24 25 Running head: Phylogeny and evolution of Lasius and the Lasiini 26 27 Keywords: Integrated taxonomy, morphology, biogeography, convergent evolution, character 28 polarity, total-evidence. 29 30 Count of figures: 10 main text, 20 supplementary. -
Download Full Article 271.2KB .Pdf File
Memoirs of the Museum of Victoria 56(2):637-641 (1997) 28 February 1997 https://doi.org/10.24199/j.mmv.1997.56.62 BIODIVERSITY INDICATORS IN CONTRASTING VEGETATION TYPES: A CASE STUDY FROM WESTERN AUSTRALIA 1 1 1 1 1 Max Abensperg-Traun , Graham Arnold , Dion Steven , Graeme Smith , Lyn Atkins Jan Viveen 2 and Mark Gutter 2 'Division of Wildlife and Ecology, CSIRO, LMB No. 4, Midland, WA 6056, Australia department of Nature Conservation, Agricultural University, Wageningen. The Netherlands Abstract Abensperg-Traun, M., Arnold, G., Steven, D., Smith, G., Atkins, L., Viveen, J. and Gutter, M., 1997. Biodiversity indicators in contrasting vegetation types: a case study from Western Australia. Memoirs of the Museum of Victoria 56(2): 637-641. Vegetation structural diversity, species richness of plants, terrestrial arthropods and liz- ards, and the relative abundance of species within ant functional groups, were examined as indicators of faunal richness in gimlet (Eucalyptus salubris) woodlands (29 sites) and shrub- lands (27 sites) in semi-arid, agricultural Western Australia. Sites varied in grazing history (woodland) and in farming history (shrubland). Total faunal richness was not effectively predicted by any indicator variable for either vegetation type. Vegetation structural diversity and richness of plants were effective indi- cators of the richness of some faunal groups in woodland but not in shrubland. Structural lizards in diversity explained 73% ( + ve) of the pooled richness of scorpions + termites + woodland. In shrubland, no variable explained > 25% of the richness of any faunal group. Reasons for the differences in the predictive qualities of structural diversity and plant rich- ness between the vegetation types are discussed. -
Distribution of Ant Species Along an Altitudinal Transect in Continuous Rainforest in Subtropical Queensland, Australia
Memoirs of the Queensland Museum | Nature 55(2) The IBISCA-Queensland Project © The State of Queensland (Queensland Museum) 2011 PO Box 3300, South Brisbane 4101, Australia Phone 06 7 3840 7555 Fax 06 7 3846 1226 Email [email protected] Website www.qm.qld.gov.au National Library of Australia card number ISSN 0079-8835 NOTE Papers published in this volume and in all previous volumes of the Memoirs of the Queensland Museum may be reproduced for scientific research, individual study or other educational purposes. Properly acknowledged quotations may be made but queries regarding the republication of any papers should be addressed to the Editor in Chief. Copies of the journal can be purchased from the Queensland Museum Shop. A Guide to Authors is displayed at the Queensland Museum web site A Queensland Government Project Typeset at the Queensland Museum Distribution of ant species along an altitudinal transect in continuous rainforest in subtropical Queensland, Australia Chris J. BURWELL Akihiro NAKAMURA Biodiversity Program, Queensland Museum, PO Box 3300, South Brisbane Qld 4101, Australia. Environmental Futures Centre and Griffith School of Environment, Griffith University, Nathan Qld 4111, Australia. Citation: Burwell, C.J. & Nakamura, A. 2011 12 20: Distribution of ant species along an altitudinal transect in continuous rainforest in subtropical Queensland, Australia. Memoirs of the Queensland Museum — Nature 55(2): 391-411. Brisbane. ISSN 0079-8835. ABSTRACT We present the distributions of ant species along an altitudinal gradient from 300 to 1100 m above sea level (m a.s.l.) within continuous rainforest in subtropical Queensland, Australia. Ants were collected along a single transect from four replicate plots at each of five zones of elevation (300, 500, 700, 900 and 1100 m a.s.l.) using a large array of methods targeting a wide range of microhabitats. -
Anicdotes • ISSUE 3 OCTOBER 2013
1 ISSUE 3 • OCTOBER 2013 The official newsletter of the Australian National Insect Collection CSIRO ECOSYTEM SCIENCES www.csiro.au Our third issue Like us on Facebook David Yeates, Director, and Beth Mantle, Manager, ANIC INSIDE THIS ISSUE It has been another very busy 6 months in ANIC. In July collections at the Professor Tim Senden hosted a microCT scanning and 3D Pacific Science Our third issue .........................................................1 imaging workshop for ANIC staff at ANU, and you can read Intercongress in Fiji more about that workshop in this edition. Postdoctoral Fellow in July. The workshop MicroCT Scanning Course ......................................2 Karen Meusemann joined ANIC from Bernie Misof’s lab in was presented as a Book Launch: Australian Longhorn Beetles Museum Koenig Germany to work on Dipteran phylogenomics. webinar to enable (Coleoptera: Cerambycidae). Vol. 1 .........................3 In September David Yeates, Adam Slipinski and Karen remote attendance, Meusemann attended workshops and conferences in Germany and you can hear Professor J.F.R Kerr’s butterfly collection donated for the 1000 insect transcriptome evolution project (1KITE), their presentations to ANIC ...................................................................4 and for the 6TH Dresden Meeting on Insect Phylogeny. here. David Yeates Beth Mantle Digitisation Update................................................. 5 The last few months has also seen the publication of two In September, ANIC major books that Adam Slipinski has -
Synonymic List of Neotropical Ants (Hymenoptera: Formicidae)
BIOTA COLOMBIANA Special Issue: List of Neotropical Ants Número monográfico: Lista de las hormigas neotropicales Fernando Fernández Sebastián Sendoya Volumen 5 - Número 1 (monográfico), Junio de 2004 Instituto de Ciencias Naturales Biota Colombiana 5 (1) 3 -105, 2004 Synonymic list of Neotropical ants (Hymenoptera: Formicidae) Fernando Fernández1 and Sebastián Sendoya2 1Profesor Asociado, Instituto de Ciencias Naturales, Facultad de Ciencias, Universidad Nacional de Colombia, AA 7495, Bogotá D.C, Colombia. [email protected] 2 Programa de Becas ABC, Sistema de Información en Biodiversidad y Proyecto Atlas de la Biodiversidad de Colombia, Instituto Alexander von Humboldt. [email protected] Key words: Formicidae, Ants, Taxa list, Neotropical Region, Synopsis Introduction Ant Phylogeny Ants are conspicuous and dominant all over the All ants belong to the family Formicidae, in the superfamily globe. Their diversity and abundance both peak in the tro- Vespoidea, within the order Hymenoptera. The most widely pical regions of the world and gradually decline towards accepted phylogentic schemes for the superfamily temperate latitudes. Nonetheless, certain species such as Vespoidea place the ants as a sister group to Vespidae + Formica can be locally abundant in some temperate Scoliidae (Brother & Carpenter 1993; Brothers 1999). countries. In the tropical and subtropical regions numerous Numerous studies have demonstrated the monophyletic species have been described, but many more remain to be nature of ants (Bolton 1994, 2003; Fernández 2003). Among discovered. Multiple studies have shown that ants represent the most widely accepted characters used to define ants as a high percentage of the biomass and individual count in a group are the presence of a metapleural gland in females canopy forests. -
Wildlife Trade Operation Proposal - Queen Ant Harvesting
Wildlife Trade Operation Proposal - Queen Ant Harvesting 1. Title and Introduction 1.1/1.2 Scientific and Common Names Please refer to Attachment A, outlining the ant species subject to harvest, giving both scientific and common names where applicable (some species are only referred to by their scientific name) and the proposed annual harvest quota which will not be exceeded. 1.3 Location of harvest Harvest will be conducted on two privately owned properties in McCrae Victoria, and one privately owned property at Forrest Lake in Queensland. 1.4 Description of what is being harvested Please refer to Attachment A for an outline of the species to be harvested. The harvest is of live, newly mated, adult queen ants. 1.5 Is the species protected under State or Federal legislation Ants are non-listed invertebrates and are as such unprotected under Victorian or Queensland 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 or Queensland legislation will be harvested. 2. Statement of general goal/aims The applicant began collecting queen ants and watching them build colonies as a personal hobby, during which time he has identified strong interest from international collectors in acquiring species of ants found in Australia. The goal of this application is to seek approval for a WTO to export queen ants. The ability to export queen ants will also increase the export sales of specialized ant keeping equipment, manufactured in Australia, to overseas ant keepers. -
Common Names for Australian Ants (Hymenoptera: Formicidae)
Australian Journal of Entomology (2002) 41, 285–293 Common names for Australian ants (Hymenoptera: Formicidae) Alan N Andersen CSIRO Sustainable Ecosystems, Tropical Ecosystems Research Centre, PMB 44, Winnellie, NT 0822, Australia. Abstract Most insects do not have common names, and this is a significant barrier to public interest in them, and to their study by non-specialists. This holds for even highly familiar insect groups such as ants. Here, I propose common names for all major native Australian ant genera and species-groups, as well as for many of the most abundant and distinctive species. Sixty-two genera, 142 species-groups and 50 species are given names. The naming system closely follows taxonomic structure; typically a genus is given a general common name, under which species-group and species names are nested. Key words ant species, communicating entomology, species-groups, taxonomic nomenclature. INTRODUCTION ‘little black ones’ (the remaining several thousand Australian species). Here, I attempt to redress this situation by propos- Common names are powerful aids for the popular communi- ing common names for all major native Australian ant genera cation of information about plant and animal species. Such and species-groups, as well as for many abundant and names use familiar and easily remembered words, in contrast distinctive species. to the taxonomic nomenclature that is so daunting for most people without formal scientific training. All higher-profile vertebrates and vascular plants have widely accepted common names. These increase the accessibility of these species to a PROPOSED ANT COMMON NAMES wide public audience, and promote interest in them. In Proposed common names, and explanations for them, for contrast, the vast majority of insects and other arthropods 62 genera, 142 species-groups and 50 species of Australian have no common name beyond the ordinal level, unless they ants are presented in Appendix I, Table A1.