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The Ants of the Genus Odontomachus (Insecta: Hymenoptera: Formicidae) in Japan
Species Diversity, 2007, 12, 89–112 The Ants of the Genus Odontomachus (Insecta: Hymenoptera: Formicidae) in Japan Masashi Yoshimura1,2, Keiichi Onoyama2,3 and Kazuo Ogata1 1 Institute of Tropical Agriculture, Kyushu University, Fukuoka, 812-8581 Japan E-mail: [email protected] 2 Course of Biotic Environment, the United Graduate School of Agricultural Sciences, Iwate University, Department of Agro-Environmental Science, Graduate School of Obihiro University, Inada-cho, Obihiro, Hokkaido, 080-8555 Japan 3 Nishi 21, Minami 4-11-9, Obihiro, Hokkaido, 080-2471 Japan (present address) (Received 22 May 2006; Accepted 18 January 2007) Species of the ant genus Odontomachus in Japan are revised. Type com- parison and detailed morphological analysis show that O. kuroiwae (Ma- tsumura, 1912) is an independent species from O. monticola Emery, 1892 and that the former species is distributed in Okinawa Island and Okinoerabu Is- land in the Ryukyu Islands. Lectotypes of both species are designated. All three castes of O. kuroiwae and O. monticola are characterized. All castes of O. kuroiwae, and the worker and male of O. monticola, are illustrated with scanning electron micrographs and light micrographs. The queen of O. kuroiwae is described for the first time. Odontomachus kuroiwae and O. mon- ticola are morphologically distinguished and taxonomically discussed. Our morphological analysis suggested that O. monticola consists of a complex of several species. Additional notes on the morphology and distribution of both species in Japan are also given. Key Words: Insecta, Hymenoptera, Formicidae, Odontomachus kuroiwae, Odontomachus monticola, worker, queen, male, taxonomy. Introduction The genus Odontomachus contains large-sized ants belonging to the tribe Ponerini of the subfamily Ponerinae (Bolton 2003). -
Morphology of the Novel Basimandibular Gland in the Ant Genus Strumigenys (Hymenoptera, Formicidae)
insects Article Morphology of the Novel Basimandibular Gland in the Ant Genus Strumigenys (Hymenoptera, Formicidae) Chu Wang 1,* , Michael Steenhuyse-Vandevelde 1, Chung-Chi Lin 2 and Johan Billen 1 1 Zoological Institute, University of Leuven, Naamsestraat 59, Box 2466, B-3000 Leuven, Belgium; [email protected] (M.S.-V.); [email protected] (J.B.) 2 Department of Biology, National Changhua University of Education, Changhua 50007, Taiwan; [email protected] * Correspondence: [email protected] Simple Summary: Ants form a diverse group of social insects that are characterized by an over- whelming variety of exocrine glands, that play a key function in the communication system and social organization of the colony. Our focus goes to the genus Strumigenys, that comprise small slow-moving ants that mainly prey on springtails. We discovered a novel gland inside the mandibles of all 22 investigated species, using light and electron microscopy. As the gland occurs close to the base of the mandibles, we name it ‘basimandibular gland’ according to the putative description given to this mandible region in a publication by the eminent British ant taxonomist Barry Bolton in 1999. The gland exists in both workers and queens and appeared most developed in the queens of Strumigenys mutica. These queens in addition to the basimandibular gland also have a cluster of gland cells near the tip of their mandibles. The queens of this species enter colonies of other Strumigenys species and parasitize on them. We expect that the peculiar development of these glands inside the mandibles of these S. mutica queens plays a role in this parasitic lifestyle, and hope that future research can shed more light on the biology of these ants. -
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. -
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 -
American Scientist the Magazine of Sigma Xi, the Scientific Research Society
A reprint from American Scientist the magazine of Sigma Xi, The Scientific Research Society This reprint is provided for personal and noncommercial use. For any other use, please send a request to Permissions, American Scientist, P.O. Box 13975, Research Triangle Park, NC, 27709, U.S.A., or by electronic mail to [email protected]. ©Sigma Xi, The Scientific Research Society and other rightsholders Sightings Serious Science, Comic-Book Style More than 300 live harvester ants, Pogonomyrmex occidentalis, are on display in the ant farm that welcomes visitors to the The Field Museum temporary exhibit The Romance of Ants. Pho- tograph by Karen Bean. he people who create museum exhibits strive to grab attention. That’s not so simple when budgets have slimmed, but visitors’ expectations have remained super-sized. At The Field Museum in Chicago, exhibition development director TMatt Matcuk and his team recently found one way. While assembling the temporary exhibit The Romance of Ants, they stuck to some fundamentals: the universal love of story and people’s inherent interest in others. They also made it fresh by mixing media, including a comic-book style narrative and museum-grade photographs by University of Illinois biologist Alex Wild. A passion for science is conveyed through the real-life journey of Corrie Moreau, an entomologist and a museum assistant curator. Alexandra Westrich, an artist and aspiring entomologist working in Moreau’s laboratory, created the art- work. The exhibit, including the edited portion shown here, will be on view in Chicago through 2011. Moreau and Westrich described their backgrounds and this nontraditional project to American Scientist associate editor Catherine Clabby. -
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. -
Geographical Distribution of the Genus Myrmoteras, Including the Description of a New Species (Hymenoptera Formicidae) by Robert E
GEOGRAPHICAL DISTRIBUTION OF THE GENUS MYRMOTERAS, INCLUDING THE DESCRIPTION OF A NEW SPECIES (HYMENOPTERA FORMICIDAE) BY ROBERT E. GREGG Department of Biology, University of Colorado In 1925, Carlo Emery summarized the accumulated knowledge c.oncerning the .ant genus Myrmoteras in the Genera Insectorum, Fasc. 183, p. 36, and listed four species with their general distribution in portions of Malay and the East Indies. The following brief anatomical diagnosis of the genus is adapted fr.om Emery, and gives the import- ant distinguishing characteristics. Worker" monomorphic. Head relatively large and angular; eyes enormous, very convex, covering one-half to ,three-quarters of the sides of the head; ocelli pr.esent; a deep, transverse groove behind the ocelli separates a prominent occipital bulge fr.om the vertex; the bulge shows a marked median depression. Clypeus produced and with a sinuate an'terior border con- tinuing into rather sharp clypeal teeth laterally. Frontal ar.ea and epistomal suture distinct. Mandibles slightly longer than the head, approximated at their bases, narrow and almost straight, armed with long teeth evenly spaced along the medial border; the mandibular apex with two quite long, sharp teeth, the terminal one representing the recurved tip of the mandible; between these two teeth two small denticles may be present. Maxillary palps 6-seg- mented; labial palps 4-segmented. Frontal carinae obso- lete. Antennal fossae remote from the epistomal suture; antennae filiform and composed of 12 segments. Thorax resembles that of Oecophylla; pronotum and epinotum prominent and convex, mesonotum depressed and 2O 22 Psyche [March saddleshaped; mesonotal tubercles pronounced and their spiracular openings conspicuous. -
The Coexistence
Philippines only in the south. In other words, the first set ex- clusively includes species with broad distributions, whether in terms of habitat preferences or geography. The second set of species contains a set of forest-in- habiting, endemic species all belonging to BROWN's (1976) O. infandus species group. This clade is distributed from the Philippines eastwards to Fiji. In BROWN's (1976) treatment of Philippine O. infandus group species, only two species, O. infandus and O. banksi, were recognised. Brown's studies of Philippine Odontomachus were mainly based on collections by Dr. James W. Chapman (most of which are housed in the Museum of Comparative Zoology, Harvard University, Cambridge, USA). Unfortunately, ac- cording to BROWN (1976), this material "is afflicted with some problems" because of "some label uncertainties." Wrongly labelled material obviously blurred Brown's view on endemic taxa (which we will show are now more clear, based on new and correctly labelled samples). After discus- sing the difficulties, BROWN (1976) finally decided against splitting the group into four species and decided instead to describe O. banksi "provisionally as a distinct species", and then to group the remaining forms (O. infandus, O. papuanus philippinus, and a third form described here as Fig. 1: Odontomachus infandus head with terms for head O. alius sp.n.) as O. infandus. structures and mandibular dentition. In revisiting the ants of this second set, we found the characters of island populations (except for the large island taken with a Leica DFC camera attached to a Leica MZ16 of Luzon) surprisingly stable. Based on this work, a new binocular microscope by help of Image Manager IM50 or and interesting problem emerges, that of deciding which Leica Application Suite V, and were processed with He- island populations represent separate species and which licon Focus 5.1, ZereneStacker 64-bit and Adobe Photo- are only local forms of a more widely distributed species, a shop 7.0. -
List of Indian Ants (Hymenoptera: Formicidae) Himender Bharti
List of Indian Ants (Hymenoptera: Formicidae) Himender Bharti Department of Zoology, Punjabi University, Patiala, India - 147002. (email: [email protected]/[email protected]) (www.antdiversityindia.com) Abstract Ants of India are enlisted herewith. This has been carried due to major changes in terms of synonymies, addition of new taxa, recent shufflings etc. Currently, Indian ants are represented by 652 valid species/subspecies falling under 87 genera grouped into 12 subfamilies. Keywords: Ants, India, Hymenoptera, Formicidae. Introduction The following 652 valid species/subspecies of myrmecology. This species list is based upon the ants are known to occur in India. Since Bingham’s effort of many ant collectors as well as Fauna of 1903, ant taxonomy has undergone major myrmecologists who have published on the taxonomy changes in terms of synonymies, discovery of new of Indian ants and from inputs provided by taxa, shuffling of taxa etc. This has lead to chaotic myrmecologists from other parts of world. However, state of affairs in Indian scenario, many lists appeared the other running/dynamic list continues to appear on web without looking into voluminous literature on http://www.antweb.org/india.jsp, which is which has surfaced in last many years and currently periodically updated and contains information about the pace at which new publications are appearing in new/unconfirmed taxa, still to be published or verified. Subfamily Genus Species and subspecies Aenictinae Aenictus 28 Amblyoponinae Amblyopone 3 Myopopone -
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Myrmecological News 19 61-64 Vienna, January 2014 A novel intramandibular gland in the ant Tatuidris tatusia (Hymenoptera: Formicidae) Johan BILLEN & Thibaut DELSINNE Abstract The mandibles of Tatuidris tatusia workers are completely filled with glandular cells that represent a novel kind of intra- mandibular gland that has not been found in ants so far. Whereas the known intramandibular glands in ants are either epi- thelial glands of class-1, or scattered class-3 cells that open through equally scattered pores on the mandibular surface, the ducts of the numerous class-3 secretory cells of Tatuidris all converge to open through a conspicuous sieve plate at the proximal ventral side near the inner margin of each mandible. Key words: Exocrine glands, mandibles, histology, Agroecomyrmecinae. Myrmecol. News 19: 61-64 (online 16 August 2013) ISSN 1994-4136 (print), ISSN 1997-3500 (online) Received 31 May 2013; revision received 5 July 2013; accepted 16 July 2013 Subject Editor: Alexander S. Mikheyev Johan Billen (contact author), Zoological Institute, University of Leuven, Naamsestraat 59, box 2466, B-3000 Leuven, Belgium. E-mail: [email protected] Thibaut Delsinne, Biological Assessment Section, Royal Belgian Institute of Natural Sciences, Rue Vautier 29, B-1000 Brussels, Belgium. E-mail: [email protected] Introduction Ants are well known as walking glandular factories, with that T. tatusia is a top predator of the leaf-litter food web an impressive overall variety of 75 glands recorded so far (JACQUEMIN & al. in press). We took advantage of the for the family (BILLEN 2009a). The glands are not only availability of two live specimens to carry out a first study found in the head, thorax and abdomen, but also occur in of the internal morphology in the Agroecomyrmecinae. -
The Functions and Evolution of Social Fluid Exchange in Ant Colonies (Hymenoptera: Formicidae) Marie-Pierre Meurville & Adria C
ISSN 1997-3500 Myrmecological News myrmecologicalnews.org Myrmecol. News 31: 1-30 doi: 10.25849/myrmecol.news_031:001 13 January 2021 Review Article Trophallaxis: the functions and evolution of social fluid exchange in ant colonies (Hymenoptera: Formicidae) Marie-Pierre Meurville & Adria C. LeBoeuf Abstract Trophallaxis is a complex social fluid exchange emblematic of social insects and of ants in particular. Trophallaxis behaviors are present in approximately half of all ant genera, distributed over 11 subfamilies. Across biological life, intra- and inter-species exchanged fluids tend to occur in only the most fitness-relevant behavioral contexts, typically transmitting endogenously produced molecules adapted to exert influence on the receiver’s physiology or behavior. Despite this, many aspects of trophallaxis remain poorly understood, such as the prevalence of the different forms of trophallaxis, the components transmitted, their roles in colony physiology and how these behaviors have evolved. With this review, we define the forms of trophallaxis observed in ants and bring together current knowledge on the mechanics of trophallaxis, the contents of the fluids transmitted, the contexts in which trophallaxis occurs and the roles these behaviors play in colony life. We identify six contexts where trophallaxis occurs: nourishment, short- and long-term decision making, immune defense, social maintenance, aggression, and inoculation and maintenance of the gut microbiota. Though many ideas have been put forth on the evolution of trophallaxis, our analyses support the idea that stomodeal trophallaxis has become a fixed aspect of colony life primarily in species that drink liquid food and, further, that the adoption of this behavior was key for some lineages in establishing ecological dominance. -
THE TRUE ARMY ANTS of the INDO-AUSTRALIAN AREA (Hymenoptera: Formicidae: Dorylinae)
Pacific Insects 6 (3) : 427483 November 10, 1964 THE TRUE ARMY ANTS OF THE INDO-AUSTRALIAN AREA (Hymenoptera: Formicidae: Dorylinae) By Edward O. Wilson BIOLOGICAL LABORATORIES, HARVARD UNIVERSITY, CAMBRIDGE, MASS., U. S. A. Abstract: All of the known Indo-Australian species of Dorylinae, 4 in Dorylus and 34 in Aenictus, are included in this revision. Eight of the Aenictus species are described as new: artipus, chapmani, doryloides, exilis, huonicus, nganduensis, philiporum and schneirlai. Phylo genetic and numerical analyses resulted in the discarding of two extant subgenera of Aenictus (Typhlatta and Paraenictus) and the loose clustering of the species into 5 informal " groups" within the unified genus Aenictus. A consistency test for phylogenetic characters is discussed. The African and Indo-Australian doryline species are compared, and available information in the biology of the Indo-Australian species is summarized. The " true " army ants are defined here as equivalent to the subfamily Dorylinae. Not included are species of Ponerinae which have developed legionary behavior independently (see Wilson, E. O., 1958, Evolution 12: 24-31) or the subfamily Leptanillinae, which is very distinct and may be independent in origin. The Dorylinae are not as well developed in the Indo-Australian area as in Africa and the New World tropics. Dorylus itself, which includes the famous driver ants, is centered in Africa and sends only four species into tropical Asia. Of these, the most widespread reaches only to Java and the Celebes. Aenictus, on the other hand, is at least as strongly developed in tropical Asia and New Guinea as it is in Africa, with 34 species being known from the former regions and only about 15 from Africa.