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Bugs R All FINAL Apr 2014 R
ISSN 2230 ! 7052 Newsletter of the $WIU4#NNInvertebrate Conservation & Information Network of South Asia (ICINSA) No. 21, April 2014 Photo: Aniruddha & Vishal Vishal Aniruddha & Photo: Contents Pages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`'%,"*4"5';*a'"9)'.%$,'4+"8*(#-,L"b;*&'/$L"U*>7+*"?$*>%,7" ;5#82.'7-2#$'/B<&L'#'67#0"#4"#0'G """## """## """# """## """## """## """ """## """## """## """#"""""""""""""""""""""@PH"WQ 6'/&/2+"/0"47%"(/47"7&#"-"'#*%".43*#",""8$*(%$"B^%#'>/#4%$*C"^*,'/=*(#'>*%E"/)"F)>'*)"6*>*("D$%%.0&*8%-"5%".,"#"$$" -
Early Behavioral and Molecular Events Leading to Caste Switching in the Ant Harpegnathos
Downloaded from genesdev.cshlp.org on September 25, 2021 - Published by Cold Spring Harbor Laboratory Press Early behavioral and molecular events leading to caste switching in the ant Harpegnathos Comzit Opachaloemphan,1,5 Giacomo Mancini,2,5 Nikos Konstantinides,2,5 Apurva Parikh,2 Jakub Mlejnek,2 Hua Yan,1,3,4 Danny Reinberg,1,3,6 and Claude Desplan2,6 1Department of Biochemistry and Molecular Pharmacology, New York University School of Medicine, New York, New York 10016, USA; 2Department of Biology, New York University, New York, New York 10003, USA; 3Howard Hughes Medical Institute, New York University School of Medicine, New York, New York 10016, USA Ant societies show a division of labor in which a queen is in charge of reproduction while nonreproductive workers maintain the colony. In Harpegnathos saltator, workers retain reproductive ability, inhibited by the queen phero- mones. Following the queen loss, the colony undergoes social unrest with an antennal dueling tournament. Most workers quickly abandon the tournament while a few workers continue the dueling for months and become gamergates (pseudoqueens). However, the temporal dynamics of the social behavior and molecular mechanisms underlining the caste transition and social dominance remain unclear. By tracking behaviors, we show that the gamergate fate is accurately determined 3 d after initiation of the tournament. To identify genetic factors responsible for this commitment, we compared transcriptomes of different tissues between dueling and nondueling workers. We found that juvenile hormone is globally repressed, whereas ecdysone biosynthesis in the ovary is increased in gamergates. We show that molecular changes in the brain serve as earliest caste predictors compared with other tissues. -
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. -
A Subgeneric Revision of Crematogaster and Discussion of Regional Species-Groups (Hymenoptera: Formicidae)
Zootaxa 3482: 47–67 (2012) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA Copyright © 2012 · Magnolia Press Article ISSN 1175-5334 (online edition) urn:lsid:zoobank.org:pub:42F5ABE3-37EC-48D6-AB1A-357BCC93DF68 A subgeneric revision of Crematogaster and discussion of regional species-groups (Hymenoptera: Formicidae) BONNIE B. BLAIMER Department of Entomology, University of California-Davis, One Shields Ave, Davis, CA 95616. E-mail: [email protected]; [email protected] Abstract Crematogaster ants are diverse, widespread and abundant in tropical, subtropical and warm-temperate climates throughout the world. The species diversity of this genus has been notoriously difficult to manage based upon morphology alone, and former attempts have generated a vaguely defined subgeneric system. I propose an improvement of the previous subgeneric classification and recognize two subgenera based upon a concurrent molecular study of the global diversity of these ants. Five of 13 former subgenera of Crematogaster are hereby synonymised under the subgenus Orthocrema Santschi: Neocrema Santschi syn. nov., Eucrema Santschi syn. nov., Rhachiocrema Mann syn. nov., Mesocrema Santschi syn. nov. and Apterocrema Wheeler syn. nov.. The eight remaining subgenera are synonymised under the subgenus Crematogaster sensu stricto: Decacrema Forel syn. nov., Oxygyne Forel syn. nov., Atopogyne Forel syn. nov., Sphaerocrema Santschi syn. nov., Colobocrema Wheeler syn. nov., Paracrema Santschi syn. nov., Physocrema Forel syn. nov. and Xiphocrema Forel syn. nov.. I present keys, morphological diagnoses and illustrations for the two revised, globally distributed subgenera Orthocrema and Crematogaster sensu stricto, based upon the worker caste. The two subgenera can be distinguished from each other by a combination of features of the petiole, postpetiole and propodeal spiracle. -
Model Organisms
RESEARCH HIGHLIGHTS Nature Reviews Genetics | Published online 30 Aug 2017; doi:10.1038/nrg.2017.70 P. Morgan/Macmillan Publishers Limited Morgan/Macmillan P. its caste-specific RNA expression is conserved in other insect species with different social systems. In ants undergoing the worker–gamergate transition, high corazonin peptide levels promoted worker-specific behaviour and inhibited behaviours associated with progression to the MODEL ORGANISMS gamergate caste; as expected, short interfering RNA (siRNA) knockdown of the corazonin receptor (CrzR) gene New tools, new insights — had the opposite phenotypic effect. The researchers went on to identify the vitellogenin gene as a key regula- probing social behaviour in ants tory target of corazonin; its expres- sion is consistently downregulated Eusocial insects display complex strategy of Harpegnathos saltator to in response to increased corazonin social behaviours, but the underlying increase the number of reproducing levels, suggesting that corazonin and Until now, molecular mechanisms are largely ants to enable them to establish orco vitellogenin have opposing effects functional unknown. Now, a trio of papers in mutant lines. In the absence of a on caste identity. Consistent with genetic studies Cell decribe two genes (orco and queen, non-reproductive H. saltator this hypothesis, siRNA knockdown corazonin) that control social behav- workers can become ‘gamergates’, of vitellogenin gene expression pro- have not been iour in ants. Furthermore, two of which lay fertilized eggs. This caste moted worker-specific behaviours. possible in the studies describe the first mutant transition can be replicated in the lab Based on these observations, the ants lines in ants, which were generated by simply by isolating workers. -
THE ANTS of the GENUS METAPONE FOREL.* Downloaded from by WILLIAM MORTON WHEELER
ANN ALS OF The Entomological Society of America Volume XII SEPTEMBER, 1919 Number 3 THE ANTS OF THE GENUS METAPONE FOREL.* Downloaded from By WILLIAM MORTON WHEELER. The singular genus Metapone was established by Forel, in 1911t, for an ant from Ceylon, M. greeni, characterized by a peculiar Ponerine habitus (resemblance to Cylindromyrmex and Simopone), scrobed head, supposedly ll-jointed antennre in the http://aesa.oxfordjournals.org/ male as well as in the worker and female, one-jointed maxillary and three-jointed labial palpi, terminally spinose or dentate middle and hind tibire and metatarsi and what he regarded as an unusually slender, strongly segmented, non-tuberculate larva, with long sparse hairs, and stout mandibles, and pupating without spinning a cocoon. He says of this genus, which he made the type of a new tribe, Metaponini: "I regard it as constituting a special section, which I place provisionally by guest on June 7, 2016 among the Ponerinre and which I call Promyrmicinre. Perhaps later it will be necessary to transfer it to the Myrmicinre. I reserve my opinion in regard to this matter," etc. A year later, Emeryt examined M. greeni and its larva more critically and found that alcoholic specimens of the latter when properly softened and expanded had the usual shape of body, head and mouthparts of the Myrmicine larva and were furnished with long, serially arranged, hooked, dorsal hairs unlike any known Ponerine larvre, but like many larval Myrmicinre. He concluded that Metapone is a true Myrmicine ant and says: "It seems to me that the comparison of Metapone with Cylindro- myrmex and Simopone on the one hand and Sima on the other. -
Description of a New Genus of Primitive Ants from Canadian Amber
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida 8-11-2017 Description of a new genus of primitive ants from Canadian amber, with the study of relationships between stem- and crown-group ants (Hymenoptera: Formicidae) Leonid H. Borysenko Canadian National Collection of Insects, Arachnids and Nematodes, [email protected] Follow this and additional works at: http://digitalcommons.unl.edu/insectamundi Part of the Ecology and Evolutionary Biology Commons, and the Entomology Commons Borysenko, Leonid H., "Description of a new genus of primitive ants from Canadian amber, with the study of relationships between stem- and crown-group ants (Hymenoptera: Formicidae)" (2017). Insecta Mundi. 1067. http://digitalcommons.unl.edu/insectamundi/1067 This Article is brought to you for free and open access by the Center for Systematic Entomology, Gainesville, Florida at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Insecta Mundi by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. INSECTA MUNDI A Journal of World Insect Systematics 0570 Description of a new genus of primitive ants from Canadian amber, with the study of relationships between stem- and crown-group ants (Hymenoptera: Formicidae) Leonid H. Borysenko Canadian National Collection of Insects, Arachnids and Nematodes AAFC, K.W. Neatby Building 960 Carling Ave., Ottawa, K1A 0C6, Canada Date of Issue: August 11, 2017 CENTER FOR SYSTEMATIC ENTOMOLOGY, INC., Gainesville, FL Leonid H. Borysenko Description of a new genus of primitive ants from Canadian amber, with the study of relationships between stem- and crown-group ants (Hymenoptera: Formicidae) Insecta Mundi 0570: 1–57 ZooBank Registered: urn:lsid:zoobank.org:pub:C6CCDDD5-9D09-4E8B-B056-A8095AA1367D Published in 2017 by Center for Systematic Entomology, Inc. -
Genetic Mechanisms Underlying the Evolutionary Success of Eusocial Insects
insects Review (Epi)Genetic Mechanisms Underlying the Evolutionary Success of Eusocial Insects Kayli R. Sieber 1 , Taylor Dorman 1, Nicholas Newell 1 and Hua Yan 1,2,* 1 Department of Biology, University of Florida, Gainesville, FL 32611, USA; kayli.sieber@ufl.edu (K.R.S.); taylor.dorman@ufl.edu (T.D.); nicholas.newell@ufl.edu (N.N.) 2 Center for Smell and Taste, University of Florida, Gainesville, FL 32611, USA * Correspondence: hua.yan@ufl.edu; Tel.: +1-352-273-4983 Simple Summary: Social insects, namely ants, bees, and termites, are among the most numerous and successful animals on Earth. This is due to a variety of features: highly cooperative behavior performed by colony members and their specialization on a variety of tasks. Diverse physiological and behavioral specializations are regulated not only by the genetic system, but also by the epige- netic system which alters gene expressions without modifying the genetic code. This review will summarize recent advancements in such studies in eusocial insects. Abstract: Eusocial insects, such as bees, ants, and wasps of the Hymenoptera and termites of the Blattodea, are able to generate remarkable diversity in morphology and behavior despite being genetically uniform within a colony. Most eusocial insect species display caste structures in which reproductive ability is possessed by a single or a few queens while all other colony members act Citation: Sieber, K.R.; Dorman, T.; as workers. However, in some species, caste structure is somewhat plastic, and individuals may Newell, N.; Yan, H. (Epi)Genetic switch from one caste or behavioral phenotype to another in response to certain environmental cues. -
Hymenoptera: Formicidae: Ponerinae)
Molecular Phylogenetics and Taxonomic Revision of Ponerine Ants (Hymenoptera: Formicidae: Ponerinae) Item Type text; Electronic Dissertation Authors Schmidt, Chris Alan Publisher The University of Arizona. Rights Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author. Download date 10/10/2021 23:29:52 Link to Item http://hdl.handle.net/10150/194663 1 MOLECULAR PHYLOGENETICS AND TAXONOMIC REVISION OF PONERINE ANTS (HYMENOPTERA: FORMICIDAE: PONERINAE) by Chris A. Schmidt _____________________ A Dissertation Submitted to the Faculty of the GRADUATE INTERDISCIPLINARY PROGRAM IN INSECT SCIENCE In Partial Fulfillment of the Requirements For the Degree of DOCTOR OF PHILOSOPHY In the Graduate College THE UNIVERSITY OF ARIZONA 2009 2 2 THE UNIVERSITY OF ARIZONA GRADUATE COLLEGE As members of the Dissertation Committee, we certify that we have read the dissertation prepared by Chris A. Schmidt entitled Molecular Phylogenetics and Taxonomic Revision of Ponerine Ants (Hymenoptera: Formicidae: Ponerinae) and recommend that it be accepted as fulfilling the dissertation requirement for the Degree of Doctor of Philosophy _______________________________________________________________________ Date: 4/3/09 David Maddison _______________________________________________________________________ Date: 4/3/09 Judie Bronstein -
Of Sri Lanka: a Taxonomic Research Summary and Updated Checklist
ZooKeys 967: 1–142 (2020) A peer-reviewed open-access journal doi: 10.3897/zookeys.967.54432 CHECKLIST https://zookeys.pensoft.net Launched to accelerate biodiversity research The Ants (Hymenoptera, Formicidae) of Sri Lanka: a taxonomic research summary and updated checklist Ratnayake Kaluarachchige Sriyani Dias1, Benoit Guénard2, Shahid Ali Akbar3, Evan P. Economo4, Warnakulasuriyage Sudesh Udayakantha1, Aijaz Ahmad Wachkoo5 1 Department of Zoology and Environmental Management, University of Kelaniya, Sri Lanka 2 School of Biological Sciences, The University of Hong Kong, Hong Kong SAR, China3 Central Institute of Temperate Horticulture, Srinagar, Jammu and Kashmir, 191132, India 4 Biodiversity and Biocomplexity Unit, Okinawa Institute of Science and Technology Graduate University, Onna, Okinawa, Japan 5 Department of Zoology, Government Degree College, Shopian, Jammu and Kashmir, 190006, India Corresponding author: Aijaz Ahmad Wachkoo ([email protected]) Academic editor: Marek Borowiec | Received 18 May 2020 | Accepted 16 July 2020 | Published 14 September 2020 http://zoobank.org/61FBCC3D-10F3-496E-B26E-2483F5A508CD Citation: Dias RKS, Guénard B, Akbar SA, Economo EP, Udayakantha WS, Wachkoo AA (2020) The Ants (Hymenoptera, Formicidae) of Sri Lanka: a taxonomic research summary and updated checklist. ZooKeys 967: 1–142. https://doi.org/10.3897/zookeys.967.54432 Abstract An updated checklist of the ants (Hymenoptera: Formicidae) of Sri Lanka is presented. These include representatives of eleven of the 17 known extant subfamilies with 341 valid ant species in 79 genera. Lio- ponera longitarsus Mayr, 1879 is reported as a new species country record for Sri Lanka. Notes about type localities, depositories, and relevant references to each species record are given. -
The Higher Classification of the Ant Subfamily Ponerinae (Hymenoptera: Formicidae), with a Review of Ponerine Ecology and Behavior
Zootaxa 3817 (1): 001–242 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Monograph ZOOTAXA Copyright © 2014 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3817.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:A3C10B34-7698-4C4D-94E5-DCF70B475603 ZOOTAXA 3817 The Higher Classification of the Ant Subfamily Ponerinae (Hymenoptera: Formicidae), with a Review of Ponerine Ecology and Behavior C.A. SCHMIDT1 & S.O. SHATTUCK2 1Graduate Interdisciplinary Program in Entomology and Insect Science, Gould-Simpson 1005, University of Arizona, Tucson, AZ 85721-0077. Current address: Native Seeds/SEARCH, 3584 E. River Rd., Tucson, AZ 85718. E-mail: [email protected] 2CSIRO Ecosystem Sciences, GPO Box 1700, Canberra, ACT 2601, Australia. Current address: Research School of Biology, Australian National University, Canberra, ACT, 0200 Magnolia Press Auckland, New Zealand Accepted by J. Longino: 21 Mar. 2014; published: 18 Jun. 2014 C.A. SCHMIDT & S.O. SHATTUCK The Higher Classification of the Ant Subfamily Ponerinae (Hymenoptera: Formicidae), with a Review of Ponerine Ecology and Behavior (Zootaxa 3817) 242 pp.; 30 cm. 18 Jun. 2014 ISBN 978-1-77557-419-4 (paperback) ISBN 978-1-77557-420-0 (Online edition) FIRST PUBLISHED IN 2014 BY Magnolia Press P.O. Box 41-383 Auckland 1346 New Zealand e-mail: [email protected] http://www.mapress.com/zootaxa/ © 2014 Magnolia Press All rights reserved. No part of this publication may be reproduced, stored, transmitted or disseminated, in any form, or by any means, without prior written permission from the publisher, to whom all requests to reproduce copyright material should be directed in writing. -
Springer Nature Switzerland AG 2020 C
P Poneroid Ants Ponerinae, which included the current poneroid subfamilies as well as Leptanillinae, the formicoid Roberto A. Keller1 and Christian Peeters2 subfamilies Ectatomminae and Heteroponerinae, 1Museu Nacional de História Natural e da Ciência and all the ▶ Dorylinae that do not display army- & cE3c-FCUL, Universidade de Lisboa, Lisbon, ant behavior (formerly included in the now obso- Portugal lete subfamily Cerapachyinae). Ponerinae sensu 2CNRS, Institute of Ecology and Environmental lato was defined by putative ancestral traits Sciences, Sorbonne Université, Paris, France exhibited by its members rather than the existence of shared derived characteristics. William Morton Wheeler remarked that “the Ponerinae comprises Poneroid ants are a clade composed of six well- unmistakably primitive and generalized forms and defined subfamilies that are morphologically het- therefore constitutes a group of twofold interest, erogeneous (Agroecomyrmecinae, first, as the ancestral stock of the higher subfamilies, Amblyoponinae, Apomyrminae, Paraponerinae, and second, as the oldest existing expression of Ponerinae and Proceratiinae) (Fig. 1). Poneroids social life among the Formicidae” [13]. Wheeler’s include just 11% of extant ant species, and molec- view persisted for a century, with subsequent ular data [4] recognize it as the sister group of the authors explicitly treating Ponerinae sensu lato as formicoids [12], the clade with the bulk of species an all-encompassing taxon from which the other diversity (Fig. 2). Not included in either of the subfamilies arose [5]. poneroids or formicoids are ▶ Leptanillinae and The twenty-first century has already brought Martialinae, two diminutive subfamilies com- major changes to the higher classification as sub- posed of highly specialized tiny subterranean families were redefined [2], morphological charac- workers.