Hymenoptera: Formicidae
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ORIGINAL ARTICLE a Novel Intracellular Mutualistic Bacterium in the Invasive Ant Cardiocondyla Obscurior
The ISME Journal (2016) 10, 376–388 © 2016 International Society for Microbial Ecology All rights reserved 1751-7362/16 www.nature.com/ismej ORIGINAL ARTICLE A novel intracellular mutualistic bacterium in the invasive ant Cardiocondyla obscurior Antonia Klein1,8, Lukas Schrader1,8, Rosario Gil2, Alejandro Manzano-Marín2, Laura Flórez3, David Wheeler5, John H Werren6, Amparo Latorre2,7, Jürgen Heinze1, Martin Kaltenpoth3,4, Andrés Moya2 and Jan Oettler1 1Institut für Zoologie, Universität Regensburg, Regensburg, Germany; 2Institut Canvanilles de Biodiversitat i Biologia Evolutiva (ICBiBE), Parc Cientific de la Universitat de Valencia, Paterna (Valencia), Spain; 3Max Planck Institute for Chemical Ecology, Jena, Germany; 4Johannes Gutenberg University Mainz, Institute for Zoology, Department for Evolutionary Ecology, Mainz, Germany; 5Institute of Fundamental Sciences, Massey University, Palmerston North, New Zealand; 6Department of Biology, University Rochester, Rochester, NY, USA and 7Área de Genómica y Salud de la Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)–Salud Pública, Valencia, Spain The evolution of eukaryotic organisms is often strongly influenced by microbial symbionts that confer novel traits to their hosts. Here we describe the intracellular Enterobacteriaceae symbiont of theinvasiveantCardiocondyla obscurior, ‘Candidatus Westeberhardia cardiocondylae’. Upon metamorphosis, Westeberhardia is found in gut-associated bacteriomes that deteriorate following eclosion. Only queens maintain Westeberhardia in the ovarian nurse cells from where the symbionts are transmitted to late-stage oocytes during nurse cell depletion. Functional analyses of the streamlined genome of Westeberhardia (533 kb, 23.41% GC content) indicate that neither vitamins nor essential amino acids are provided for the host. However, the genome encodes for an almost complete shikimate pathway leading to 4-hydroxyphenylpyruvate, which could be converted into tyrosine by the host. -
Key to the Workers of the 100 Ant Genera and 12 Ant Subfamilies of Borneo in English and Malay
Key to the workers of the 100 ant genera and 12 ant subfamilies of Borneo in English and Malay Adapted and updated by Tom M. Fayle from the keys written by Yoshiaki Hashimoto, with additional material from LaPolla et al 2010 (Prenolepis group genera) and Zettel and Zimmerman 2007 (Forelophilus). Translated into Malay by Kalsum M. Yusah Numbers of genera within subfamilies are for Borneo only Note that this key is still being developed. If you have any comments or constructive criticism then I would be very grateful if you email me at [email protected] This key does not yet include Tyrannomyrmex, Romblonella, and Leptothorax, nor Bregmatomyrma, which is known only from the queen. Translations in Malay are in italic following each half of each couplet Jump to key (control-click on couplet number): Subfamilies 1 Amblyoponinae 12 Proceratiinae 15 Ectatomminae 17 Ponerinae 18 Formicinae 31 Dolichoderinae 48 Myrmicinae 55 Leptanillinae 98 Key to Subfamilies 1. Mesosoma attached to the gaster by two segments (the petiole and postpetiole) each separated by distinct constrictions (a)............................................................................2 Mesosoma bersambung pada gaster terdiri daripada dua segmen (petiole dan postpetiole) segmen ini terbahagi dengan jelas (a) Mesosoma attached to gaster by a single, distinct segment, (the petiole) (A)...............3 Mesosoma bersambung pada gaster pada satu segmen sahaja, (petiole) (A) 2. Frontal lobes almost always present and expanded towards the sides so that they cover the inner -
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. -
Radiation in Socially Parasitic Formicoxenine Ants
RADIATION IN SOCIALLY PARASITIC FORMICOXENINE ANTS DISSERTATION ZUR ERLANGUNG DES DOKTORGRADES DER NATURWISSENSCHAFTEN (D R. R ER . N AT .) DER NATURWISSENSCHAFTLICHEN FAKULTÄT III – BIOLOGIE UND VORKLINISCHE MEDIZIN DER UNIVERSITÄT REGENSBURG vorgelegt von Jeanette Beibl aus Landshut 04/2007 General Introduction II Promotionsgesuch eingereicht am: 19.04.2007 Die Arbeit wurde angeleitet von: Prof. Dr. J. Heinze Prüfungsausschuss: Vorsitzender: Prof. Dr. S. Schneuwly 1. Prüfer: Prof. Dr. J. Heinze 2. Prüfer: Prof. Dr. S. Foitzik 3. Prüfer: Prof. Dr. P. Poschlod General Introduction I TABLE OF CONTENTS GENERAL INTRODUCTION 1 CHAPTER 1: Six origins of slavery in formicoxenine ants 13 Introduction 15 Material and Methods 17 Results 20 Discussion 23 CHAPTER 2: Phylogeny and phylogeography of the Mediterranean species of the parasitic ant genus Chalepoxenus and its Temnothorax hosts 27 Introduction 29 Material and Methods 31 Results 36 Discussion 43 CHAPTER 3: Phylogenetic analyses of the parasitic ant genus Myrmoxenus 46 Introduction 48 Material and Methods 50 Results 54 Discussion 59 CHAPTER 4: Cuticular profiles and mating preference in a slave-making ant 61 Introduction 63 Material and Methods 65 Results 69 Discussion 75 CHAPTER 5: Influence of the slaves on the cuticular profile of the slave-making ant Chalepoxenus muellerianus and vice versa 78 Introduction 80 Material and Methods 82 Results 86 Discussion 89 GENERAL DISCUSSION 91 SUMMARY 99 ZUSAMMENFASSUNG 101 REFERENCES 103 APPENDIX 119 DANKSAGUNG 120 General Introduction 1 GENERAL INTRODUCTION Parasitism is an extremely successful mode of life and is considered to be one of the most potent forces in evolution. As many degrees of symbiosis, a phenomenon in which two unrelated organisms coexist over a prolonged period of time while depending on each other, occur, it is not easy to unequivocally define parasitism (Cheng, 1991). -
Easychair Preprint Ant Microbial Endosymbionts and the Emergent
EasyChair Preprint № 1661 Ant microbial endosymbionts and the emergent properties of social groups Alessio Sclocco, Shirlyn Jia Yun Ong and Serafino Teseo EasyChair preprints are intended for rapid dissemination of research results and are integrated with the rest of EasyChair. October 14, 2019 Ant microbial endosymbionts and the emergent properties of social groups Alessio Sclocco1, Shirlyn Jia Yun Ong2 and Serafino Teseo2† 1Netherlands eScience Center, Amsterdam, The Netherlands (E-mail: [email protected]) 2School of Biological Sciences, Nanyang Technological University, Singapore (Tel: +65 63167088; E-mail: [email protected]) Abstract: In the last fifteen years, research on animal models has provided advances on how gut symbiotic microbes affect behavior and its underlying neurophysiology. However, most studies on the gut microbiota only take into exam individual behavior without considering social dynamics. Contrarily, animals and humans live in complex societies where they constantly adjust physiology and behavior to social interactions. To improve our understanding of how microbes and hosts interact and produce functional individual, social and collective phenotypes, we need to broaden our experimental approaches to a group-level dimension. The ideal models for this purpose are social animals living in stable symbioses with microbes, such as eusocial insects. In our research, we investigate Camponotus carpenter ants and their obligate bacterial symbiont Blochmannia from a behavioral ecology perspective. We aim to create ant colonies including differential proportions of bacteria-free individuals by suppressing Blochmannia with antibiotics. Then, using a machine learning-based video tracking system, we will study network features and group-level behavior of such experimental colonies. Keywords: Social Evolution; Microbiota-Gut-Brain Axis; Ants; Group-Level Behavior; Machine Learning; Real Time Data Analysis 1. -
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. -
Second Species in the Australian Ant Genus Peronomyrmexviehmeyer (Hymenoptera: Formicidae) Steven O Shattuck1* and Simon Hinkley2
Australian Journal of Entomology (2002) 41, 104–105 Second species in the Australian ant genus PeronomyrmexViehmeyer (Hymenoptera: Formicidae) Steven O Shattuck1* and Simon Hinkley2 1CSIRO Entomology, GPO Box 1700, Canberra, ACT 2601, Australia. 2Museum Victoria, GPO Box 666E, Melbourne, Vic. 3001, Australia. Abstract A second species of the rare Australian ant genus Peronomyrmex is described from Victoria. This new species, P. bartoni, represents only the third time the genus has been collected, the previous records being the holotype of P. overbecki Viehmeyer from north-eastern New South Wales and a collection, subsequently lost, from northern Queensland. Key words Australia, Formicidae, Hymenoptera, new species, Peronomyrmex. INTRODUCTION Description. Total length 4.3 mm; maximum head length 1.04 mm; maximum head width (behind eyes) 0.84 mm; Until recently, the Australian ant genus Peronomyrmex maximum diameter of eye 0.24 mm; scape length 0.62 mm; Viehmeyer has been known from only a single collection con- cephalic index 81; scape index 74; width across pronotal sisting of a single worker from north-eastern New South humeri 0.64 mm; Weber’s length of thorax 1.21 mm; dorsal Wales. While a second series had been collected from north- petiole width 0.26 mm; maximum petiole height 0.56 mm; ern Queensland, it was lost before it could be studied in detail dorsal postpetiole width 0.40 mm; maximum postpetiole (Shattuck 1999). The original specimen was described by height 0.62 mm. Head capsule (Fig. 1) with distinct, longi- Viehmeyer (1922) in the newly established genus Perono- tudinal rugae, those on dorsal surface between antennal myrmex as P. -
Invasive Ant Pest Risk Assessment Project: Preliminary Risk Assessment
Invasive ant pest risk assessment project: Preliminary risk assessment Harris, R. 1) Aim To assess the threat to New Zealand of a wide range of ant species not already established in New Zealand and identify those worthy of more detailed assessment. 2) Scope 2.1. Specific exclusions Solenopsis invicta was specifically excluded from consideration as this species has already been subject to detailed consideration by Biosecurity New Zealand. 2.2 Specific inclusions Biosecurity New Zealand requested originally that the following taxa be included in the assessment: Solenopsis richteri Solenopsis geminata Wasmannia auropunctata Anoplolepis gracilipes Paratrechina longicornis Carpenter ants (Camponotus spp.) Leaf cutting ants (Atta spp.) Myrmecia pilosula Tapinoma melanocephalum Monomorium sydneyense (incursion found in New Zealand) Hypoponera punctatissima (incursion found in New Zealand) Big headed ants (Pheidole spp.) M. sydneyense and H. punctatissima have since been deemed not under official control and are now considered established in New Zealand. Profiles of these species have been prepared as part of the Ants of New Zealand section (see http://www.landcareresearch.co.nz/research/biosecurity/stowaways/Ants/antsinnewzealand.asp). INVASIVE ANT PEST RISK ASSESSMENT PROJECT: Preliminary risk assessment 3) Methodology A risk assessment scorecard was developed (Appendix 1) in consultation with a weed risk assessment expert (Dr Peter Williams) and with Simon O’Connor and Amelia Pascoe of Biosecurity New Zealand, to initially separate -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
Hymenoptera: Formicidae
16 The Weta 30: 16-18 (2005) Changes to the classification of ants (Hymenoptera: Formicidae) Darren F. Ward School of Biological Sciences, Tamaki Campus, Auckland University, Private Bag 92019, Auckland ([email protected]) Introduction This short note aims to update the reader on changes to the subfamily classification of ants (Hymenoptera: Formicidae). Although the New Zealand ant fauna is very small, these changes affect the classification and phylogeny of both endemic and exotic ant species in New Zealand. Bolton (2003) has recently proposed a new subfamily classification for ants. Two new subfamilies have been created, a revised status for one, and new status for four. Worldwide, there are now 21 extant subfamilies of ants. The endemic fauna of New Zealand is now classified into six subfamilies (Table 1), as a result of three subfamilies, Amblyoponinae, Heteroponerinae and Proceratiinae, being split from the traditional subfamily Ponerinae. Bolton’s (2003) classification also affects several exotic species in New Zealand. Three species have been transferred from Ponerinae: Amblyopone australis to Amblyoponinae, and Rhytidoponera chalybaea and R. metallica to Ectatomminae. Currently there are 28 exotic species in New Zealand (Table 1). Eighteen species have most likely come from Australia, where they are native. Eight are global tramp species, commonly transported by human activities, and two species are of African origin. Nineteen of the currently established exotic species are recorded for the first time in New Zealand as occurring outside their native range. This may result in difficulty in obtaining species-specific biological knowledge and assessing their likelihood of becoming successful invaders. In addition to the work by Bolton (2003), Phil Ward and colleagues at UC Davis have started to resolve the phylogenetic relationships among subfamilies and genera of all ants using molecular data (Ward et al, 2005). -
Diversity of Bacteria in Ants (Hymenoptera: Formicidae) from Canopy and Understory of Selected Trees at Mount Makiling Forest Reserve, Laguna, Philippines
Philippine Journal of Science 150 (3): 753-763, June 2021 ISSN 0031 - 7683 Date Received: 30 Sep 2020 Diversity of Bacteria in Ants (Hymenoptera: Formicidae) from Canopy and Understory of Selected Trees at Mount Makiling Forest Reserve, Laguna, Philippines Michael P. Gatpatan1, Mia Beatriz C. Amoranto1, Alfredo Jose C. Ballesteros3, Noel G. Sabino1, Jocelyn T. Zarate2, Ma. Anita M. Bautista3, and Lucille C. Villegas1* 1Microbiology Division, Institute of Biological Sciences 2National Institute of Molecular Biology and Biotechnology (BIOTECH) University of the Philippines Los Baños, College, Laguna 4031 Philippines 3National Institute of Molecular Biology and Biotechnology (NIMBB) University of the Philippines Diliman, Quezon City 1101 Philippines The Mount Makiling Forest Reserve (MMFR) is a biodiversity hotspot and listed as one of the 170 conservation priority areas established by the Philippine government. Its flora and fauna diversity has been reported, but knowledge gap has been identified concerning the bacterial communities associated with the flora and fauna. This study focused on ants (Hymenoptera: Formicidae), which are dominant in forest canopy and play essential roles in the ecosystem functionality. A metagenomic sequencing approach based on amplified V3–V4 regions of the 16S rRNA was employed to investigate the bacterial communities associated with five arboreal ant species collected from MMFR. The collected ants were identified as Dolichoderus thoracicus, Myrmicaria sp., Colobopsis leonardi, Polyrhachis mindanaensis, and Polyrhachis semiinermis. The sequence analyses revealed that Proteobacteria, Spirochaetes, Firmicutes, Bacteroides, and Actinobacteria were the most abundant phyla. Individual analysis of the bacterial genera associated with the five ant species showed that unclassified members of Rhizobiaceae, Orbaceae, and Burkholderiaceae were dominant in D. -
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.