A Guide to the Ants of South-Western Australia
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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) . -
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. -
Tree-Dwelling Ants: Contrasting Two Brazilian Cerrado Plant Species Without Extrafloral Nectaries
Hindawi Publishing Corporation Psyche Volume 2012, Article ID 172739, 6 pages doi:10.1155/2012/172739 Research Article Tree-Dwelling Ants: Contrasting Two Brazilian Cerrado Plant Species without Extrafloral Nectaries Jonas Maravalhas,1 JacquesH.C.Delabie,2 Rafael G. Macedo,1 and Helena C. Morais1 1 Departamento de Ecologia, Instituto de Biologia, Universidade de Bras´ılia, 70910-900 Bras´ılia, DF, Brazil 2 Laboratorio´ de Mirmecologia, Convˆenio UESC/CEPLAC, Centro de Pesquisa do Cacau, CEPLAC, Cx. P. 07, 45600-000 Itabuna, BA, Brazil Correspondence should be addressed to Jonas Maravalhas, [email protected] Received 31 May 2011; Revised 28 June 2011; Accepted 30 June 2011 Academic Editor: Fernando Fernandez´ Copyright © 2012 Jonas Maravalhas et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Ants dominate vegetation stratum, exploiting resources like extrafloral nectaries (EFNs) and insect honeydew. These interactions are frequent in Brazilian cerrado and are well known, but few studies compare ant fauna and explored resources between plant species. We surveyed two cerrado plants without EFNs, Roupala montana (found on preserved environments of our study area) and Solanum lycocarpum (disturbed ones). Ants were collected and identified, and resources on each plant noted. Ant frequency and richness were higher on R. montana (67%; 35 spp) than S. lycocarpum (52%; 26), the occurrence of the common ant species varied between them, and similarity was low. Resources were explored mainly by Camponotus crassus and consisted of scale insects, aphids, and floral nectaries on R. -
As Formigas Do Brasil
Jacques H. C. Delabie, Rodrigo M. Feitosa, José Eduardo Serrão, Cléa S. F. Mariano, Jonathan D. Majer Organizadores Jacques Delabie, Rodrigo Feitosa, José Eduardo Serrão, Cléa Mariano, Jonathan Majer As formigas Poneromorfas do Brasil Ilhéus-Bahia 2015 Copyright © 2015 by JACQUES H. C. DELABIE, RODRIGO M. FEITOSA, JOSÉ EDUARDO SERRÃO, CLÉA S. F. MARIANO, JONATHAN D. MAJER Universidade Estadual de Santa Cruz Direitos desta edição reservados à GOVERNO DO ESTADO DA BAHIA EDITUS - EDITORA DA UESC RUI COSTA - GOVERNADOR SECRETARIA DE EDUCAÇÃO OSVALDO BArrETO FILHO - SECRETÁRIO A reprodução não autorizada desta publicação, por qualquer meio, seja total ou parcial, UNIVERSIDADE ESTADUAL DE SANTA CRUZ constitui violação da Lei nº 9.610/98. ADÉLIA MARIA CArvALHO DE MELO PINHEIRO - REITORA EVANdrO SENA FREIRE - VICE-REITOR Depósito legal na Biblioteca Nacional, conforme Lei nº 10.994, de 14 de DIRETORA DA EDITUS dezembro de 2004. RITA VIRGINIA ALVES SANTOS ARGOLLO Conselho Editorial: Rita Virginia Alves Santos Argollo – Presidente Andréa de Azevedo Morégula DIAGRAMAÇÃO E CAPA André Luiz Rosa Ribeiro Alencar Júnior Adriana dos Santos Reis Lemos Dorival de Freitas FOTOS Evandro Sena Freire Retirados do site AntWeb.org Francisco Mendes Costa REVISÃO José Montival Alencar Júnior Roberto Santos de Carvalho Lurdes Bertol Rocha Jacques H. C. Delabie, Maria Laura de Oliveira Gomes Rodrigo M. Feitosa, Marileide dos Santos de Oliveira José Eduardo Serrão, Raimunda Alves Moreira de Assis Cléa S. F. Mariano, Roseanne Montargil Rocha Jonathan D. Majer Sílvia Maria Santos Carvalho Tércio S. Melo Dados Internacionais de Catalogação na Publicação (CIP) F725 As formigas poneromorfas do Brasil / Jacques H. C. Delabie...[et. -
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. -
Diversity and Organization of the Ground Foraging Ant Faunas of Forest, Grassland and Tree Crops in Papua New Guinea
- - -- Aust. J. Zool., 1975, 23, 71-89 Diversity and Organization of the Ground Foraging Ant Faunas of Forest, Grassland and Tree Crops in Papua New Guinea P. M. Room Department of Agriculture, Stock and Fisheries, Papua New Guinea; present address: Cotton Research Unit, CSIRO, P.M.B. Myallvale Mail Run, Narrabri, N.S.W. 2390. Abstract Thirty samples of ants were taken in each of seven habitats: primary forest, rubber plantation, coffee plantation, oilpalm plantation, kunai grassland, eucalypt savannah and urban grassland. Sixty samples were taken in cocoa plantations. A total of 156 species was taken, and the frequency of occurrence of each in each habitat is given. Eight stenoecious species are suggested as habitat indicators. Habitats fell into a series according to the similarity of their ant faunas: forest, rubber and coffee, cocoa and oilpalm, kunai and savannah, urban. This series represents an artificial, discontinuous succession from a complex stable ecosystem to a simple unstable one. Availability of species suitably preadapted to occupy habitats did not appear to limit species richness. Habitat heterogeneity and stability as affected by human interference did seem to account for inter-habitat variability in species richness. Species diversity was compared between habitats using four indices: Fisher et al.; Margalef; Shannon; Brillouin. Correlation of diversity index with habitat hetero- geneity plus stability was good for the first two, moderate for Shannon, and poor for Brillouin. Greatest diversity was found in rubber, the penultimate in the series of habitats according to hetero- geneity plus stability ('maturity'). Equitability exceeded the presumed maximum in rubber, and was close to the maximum in all habitats. -
James K. Wetterer
James K. Wetterer Wilkes Honors College, Florida Atlantic University 5353 Parkside Drive, Jupiter, FL 33458 Phone: (561) 799-8648; FAX: (561) 799-8602; e-mail: [email protected] EDUCATION UNIVERSITY OF WASHINGTON, Seattle, WA, 9/83 - 8/88 Ph.D., Zoology: Ecology and Evolution; Advisor: Gordon H. Orians. MICHIGAN STATE UNIVERSITY, East Lansing, MI, 9/81 - 9/83 M.S., Zoology: Ecology; Advisors: Earl E. Werner and Donald J. Hall. CORNELL UNIVERSITY, Ithaca, NY, 9/76 - 5/79 A.B., Biology: Ecology and Systematics. UNIVERSITÉ DE PARIS III, France, 1/78 - 5/78 Semester abroad: courses in theater, literature, and history of art. WORK EXPERIENCE FLORIDA ATLANTIC UNIVERSITY, Wilkes Honors College 8/04 - present: Professor 7/98 - 7/04: Associate Professor Teaching: Biodiversity, Principles of Ecology, Behavioral Ecology, Human Ecology, Environmental Studies, Tropical Ecology, Field Biology, Life Science, and Scientific Writing 9/03 - 1/04 & 5/04 - 8/04: Fulbright Scholar; Ants of Trinidad and Tobago COLUMBIA UNIVERSITY, Department of Earth and Environmental Science 7/96 - 6/98: Assistant Professor Teaching: Community Ecology, Behavioral Ecology, and Tropical Ecology WHEATON COLLEGE, Department of Biology 8/94 - 6/96: Visiting Assistant Professor Teaching: General Ecology and Introductory Biology HARVARD UNIVERSITY, Museum of Comparative Zoology 8/91- 6/94: Post-doctoral Fellow; Behavior, ecology, and evolution of fungus-growing ants Advisors: Edward O. Wilson, Naomi Pierce, and Richard Lewontin 9/95 - 1/96: Teaching: Ethology PRINCETON UNIVERSITY, Department of Ecology and Evolutionary Biology 7/89 - 7/91: Research Associate; Ecology and evolution of leaf-cutting ants Advisor: Stephen Hubbell 1/91 - 5/91: Teaching: Tropical Ecology, Introduction to the Scientific Method VANDERBILT UNIVERSITY, Department of Psychology 9/88 - 7/89: Post-doctoral Fellow; Visual psychophysics of fish and horseshoe crabs Advisor: Maureen K. -
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. -
James K. Wetterer
James K. Wetterer Wilkes Honors College, Florida Atlantic University 5353 Parkside Drive, Jupiter, FL 33458 Phone: (561) 799-8648; FAX: (561) 799-8602; e-mail: [email protected] EDUCATION UNIVERSITY OF WASHINGTON, Seattle, WA, 9/83 - 8/88 Ph.D., Zoology: Ecology and Evolution; Advisor: Gordon H. Orians. MICHIGAN STATE UNIVERSITY, East Lansing, MI, 9/81 - 9/83 M.S., Zoology: Ecology; Advisors: Earl E. Werner and Donald J. Hall. CORNELL UNIVERSITY, Ithaca, NY, 9/76 - 5/79 A.B., Biology: Ecology and Systematics. UNIVERSITÉ DE PARIS III, France, 1/78 - 5/78 Semester abroad: courses in theater, literature, and history of art. WORK EXPERIENCE FLORIDA ATLANTIC UNIVERSITY, Wilkes Honors College 8/04 - present: Professor 7/98 - 7/04: Associate Professor Teaching: Principles of Ecology, Behavioral Ecology, Human Ecology, Environmental Studies, Tropical Ecology, Biodiversity, Life Science, and Scientific Writing 9/03 - 1/04 & 5/04 - 8/04: Fulbright Scholar; Ants of Trinidad and Tobago COLUMBIA UNIVERSITY, Department of Earth and Environmental Science 7/96 - 6/98: Assistant Professor Teaching: Community Ecology, Behavioral Ecology, and Tropical Ecology WHEATON COLLEGE, Department of Biology 8/94 - 6/96: Visiting Assistant Professor Teaching: General Ecology and Introductory Biology HARVARD UNIVERSITY, Museum of Comparative Zoology 8/91- 6/94: Post-doctoral Fellow; Behavior, ecology, and evolution of fungus-growing ants Advisors: Edward O. Wilson, Naomi Pierce, and Richard Lewontin 9/95 - 1/96: Teaching: Ethology PRINCETON UNIVERSITY, Department of Ecology and Evolutionary Biology 7/89 - 7/91: Research Associate; Ecology and evolution of leaf-cutting ants Advisor: Stephen Hubbell 1/91 - 5/91: Teaching: Tropical Ecology, Introduction to the Scientific Method VANDERBILT UNIVERSITY, Department of Psychology 9/88 - 7/89: Post-doctoral Fellow; Visual psychophysics of fish and horseshoe crabs Advisor: Maureen K. -
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. -
Report on Pitfall Trapping of Ants at the Biospecies Sites in the Nature Reserve of Orange County, California
Report on Pitfall Trapping of Ants at the Biospecies Sites in the Nature Reserve of Orange County, California Prepared for: Nature Reserve of Orange County and The Irvine Co. Open Space Reserve, Trish Smith By: Krista H. Pease Robert N. Fisher US Geological Survey San Diego Field Station 5745 Kearny Villa Rd., Suite M San Diego, CA 92123 2001 2 INTRODUCTION: In conjunction with ongoing biospecies richness monitoring at the Nature Reserve of Orange County (NROC), ant sampling began in October 1999. We quantitatively sampled for all ant species in the central and coastal portions of NROC at long-term study sites. Ant pitfall traps (Majer 1978) were used at current reptile and amphibian pitfall trap sites, and samples were collected and analyzed from winter 1999, summer 2000, and winter 2000. Summer 2001 samples were recently retrieved, and are presently being identified. Ants serve many roles on different ecosystem levels, and can serve as sensitive indicators of change for a variety of factors. Data gathered from these samples provide the beginning of three years of baseline data, on which long-term land management plans can be based. MONITORING OBJECTIVES: The California Floristic Province, which includes southern California, is considered one of the 25 global biodiversity hotspots (Myers et al. 2000). The habitat of this region is rapidly changing due to pressure from urban and agricultural development. The Scientific Review Panel of the State of California's Natural Community Conservation Planning Program (NCCP) has identified preserve design parameters as one of the six basic research needs for making informed long term conservation planning decisions. -
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.