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Myrmicinae: Crematogastrini] Dacatria Rigato, 1994B: 155
DACATRIA [Myrmicinae: Crematogastrini] Dacatria Rigato, 1994b: 155. Type-species: Dacatria templaris Rigato, 1994b: 157, by original designation. Taxonomic history Dacatria in Myrmicinae, Proattini: Rigato, 1994b: 161. Dacatria in Myrmicinae, Stenammini: Bolton, 1994: 106; Bolton, 1995b: 26; Bolton, 2003: 59, 203. Dacatria in Myrmicinae, Crematogastrini: Ward, et al. 2015: 77; in Crematogastrini, Mayriella genus group: Blaimer, et al. 2018: 7. Dacatria as genus: all authors. Dacatria references: Eguchi, et al. 2011: 15 (diagnosis, Vietnam synopsis). DACETINOPS [Myrmicinae: Crematogastrini] Dacetinops Brown & Wilson, 1957a: 1. Type-species: Dacetinops cibdela Brown & Wilson, 1957: 4, by original designation. Taxonomic history Dacetinops in Myrmicinae, Leptothoracini: Wheeler, G.C. & Wheeler, J. 1985: 257. Dacetinops incertae sedis in Myrmicinae: Dlussky & Fedoseeva, 1988: 80. Dacetinops in Myrmicinae, Stenammini: Bolton, 1994: 106; Bolton, 1995b: 26; Bolton, 2003: 59, 203. Dacetinops in Myrmicinae, Crematogastrini: Ward, et al. 2015: 77; in Crematogastrini, Vollenhovia genus group: Blaimer, et al. 2018: 7. Dacetinops as genus: all authors. Dacetinops catalogues: Bolton, 1995b: 168. Dacetinops references: Taylor, 1985: 49 (all species revision, key). DACETON [Myrmicinae: Attini] Daceton Perty, 1833: 136. Type-species: Formica armigera Latreille, 1802c: 244, by monotypy. Taxonomic history Daceton in Poneridae, Myrmicidae: Smith, F. 1858b: 160. Daceton in Myrmicidae, Cryptoceridae: Smith, F. 1853: 226; Emery, 1877a: 81. Daceton in Cryptoceridae, Dacetini: Ashmead, 1905b: 384 [Dacetonini]. Daceton in Myrmicinae: Mayr, 1865: 26 [Myrmicidae]; Dalla Torre, 1893: 149 [Myrmicinae]. Daceton in Myrmicinae, Dacetini, Dacetiti: Brown, 1952g: 10 (footnote); Brown, 1954b: 465; Brown & Wilson, 1959b: 281; Brandão, 1991: 391. Daceton in Myrmicinae, Dacetini: Forel, 1893a: 164; Forel, 1892d: 344; Forel, 1895b: 136; Emery, 1895j: 770; Emery, 1896e: 180; Wheeler, W.M. -
A Guide to the Ants of Sabangau
A Guide to the Ants of Sabangau The Orangutan Tropical Peatland Project November 2014 A Guide to the Ants of Sabangau All original text, layout and illustrations are by Stijn Schreven (e-mail: [email protected]), supple- mented by quotations (with permission) from taxonomic revisions or monographs by Donat Agosti, Barry Bolton, Wolfgang Dorow, Katsuyuki Eguchi, Shingo Hosoishi, John LaPolla, Bernhard Seifert and Philip Ward. The guide was edited by Mark Harrison and Nicholas Marchant. All microscopic photography is from Antbase.net and AntWeb.org, with additional images from Andrew Walmsley Photography, Erik Frank, Stijn Schreven and Thea Powell. The project was devised by Mark Harrison and Eric Perlett, developed by Eric Perlett, and coordinated in the field by Nicholas Marchant. Sample identification, taxonomic research and fieldwork was by Stijn Schreven, Eric Perlett, Benjamin Jarrett, Fransiskus Agus Harsanto, Ari Purwanto and Abdul Azis. Front cover photo: Workers of Polyrhachis (Myrma) sp., photographer: Erik Frank/ OuTrop. Back cover photo: Sabangau forest, photographer: Stijn Schreven/ OuTrop. © 2014, The Orangutan Tropical Peatland Project. All rights reserved. Email [email protected] Website www.outrop.com Citation: Schreven SJJ, Perlett E, Jarrett BJM, Harsanto FA, Purwanto A, Azis A, Marchant NC, Harrison ME (2014). A Guide to the Ants of Sabangau. The Orangutan Tropical Peatland Project, Palangka Raya, Indonesia. The views expressed in this report are those of the authors and do not necessarily represent those of OuTrop’s partners or sponsors. The Orangutan Tropical Peatland Project is registered in the UK as a non-profit organisation (Company No. 06761511) and is supported by the Orangutan Tropical Peatland Trust (UK Registered Charity No. -
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. -
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). -
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. -
Group Recruitment in a Thermophilic Desert Ant, Ocymyrmex Robustior
Eawag_07834 J Comp Physiol A (2013) 199:711–722 DOI 10.1007/s00359-013-0830-x ORIGINAL PAPER Group recruitment in a thermophilic desert ant, Ocymyrmex robustior Stefan Sommer • Denise Weibel • Nicole Blaser • Anna Furrer • Nadine E. Wenzler • Wolfgang Ro¨ssler • Ru¨diger Wehner Received: 19 March 2013 / Revised: 30 April 2013 / Accepted: 17 May 2013 / Published online: 8 June 2013 Ó Springer-Verlag Berlin Heidelberg 2013 Abstract Thermophilic desert ants—Cataglyphis, Ocy- nest. As video recordings show the leader, while continually myrmex, and Melophorus species inhabiting the arid zones keeping her gaster in a downward position, intermittently of the Palaearctic region, southern Africa and central Aus- touches the surface of the ground with the tip of the gaster tralia, respectively—are solitary foragers, which have been most likely depositing a volatile pheromone signal. These considered to lack any kind of chemical recruitment. Here recruitment events occur during the entire diurnal activity we show that besides mainly employing the solitary mode period of the Ocymyrmex foragers, that is, even at surface of food retrieval Ocymyrmex robustior regularly exhibits temperatures of more than 60 °C. They may provide group recruitment to food patches that cannot be exploited promising experimental paradigms for studying the inter- individually. Running at high speed to recruitment sites that play of orientation by chemical signals and path integration may be more than 60 m apart from the nest a leading ant, as well as other visual guidance routines. the recruiter, is followed by a loose and often quite dis- persed group of usually 2–7 recruits, which often overtake Keywords Desert ants Á Recruitment Á Ocymyrmex Á the leader, or may lose contact, fall back and return to the Path integration Á Solitary foraging S. -
Hymenoptera: Formicidae: Myrmicinae)
INS. KOREANA, 18(3): 000~000. September 30, 2001 Review of Korean Dacetini (Hymenoptera: Formicidae: Myrmicinae) Dong-Pyeo LYU, Byeong-MOON CHOI1) and Soowon CHO Department of Agricultural Biology, Chungbuk National University, Cheongju, CB 361-763, Korea 1) Dept. of Science Education, Cheongju National University of Education, Cheongju, CB 361-150, Korea Abstract Most current systematic changes in the tribe Dacetini are applied to the Korean dacetine ants. The tribe Dacetini of Korea include Strumigenys lewisi, Pyramica incerta, P. japonica, P. mutica, and P. hexamerus. Taxonomic positions are revised, new informations are added, and a full reference list is provided. Key words Strumigenys lewisi, Pyramica incerta, P. japonica, P. mutica, P. hexamerus, Dacetini, Formicidae, Korea INTRODUCTION The Dacetini is a tribe of ants that are all predators, most of them small, cryptic elements of tropical forest leaf litter and rotten wood (Bolton, 1998). Most of them have highly modified mandibles, being different from the standard triangular mandible common to most other ants. Many have mandibles that are elongate, linear, and with opposing tines at the tip. Others have elongate mandibles like serrated scissors, or have serrated mandibles that are curved ventrally. For some time, the name Dacetini had been confused with Dacetonini. The tribe name was originated from the genus Daceton, but the genitive of daketon (“biter”) would be daketou, so the tribe name must be Dacetini, not Dacetonini. Bolton (2000) also recently found this problem and he resurrected the name Dacetini. The generic classification of the tribe up to now is the product of a series of revisionary papers mainly by Brown (1948, 1949a, b, c, 1950a, b, 1952b, 1953a, 1954a), Brown and Wilson (1959) and Brown and Carpenter (1979). -
Appendix 1 Table A1
Oikos OIK-01723 Staab, M., Blüthgen, N. and Klein, A.-M. 2014. Tree diversity alters the structure of a tri-trophic network in a biodiversity experiment. – Oikos doi: 10.1111/oik.01723 Appendix 1 Table A1. Number of trophobiotic interactions for plant, Hemiptera and ant species in an early successional tree plantation in southest China. The numbers in the first column refer to the species codes in Fig. 1, Fig. 2 and Fig. A1. Taxonomic names of plant species follows the Flora of China (<www.efloras.org/flora_page.aspx?flora_id=2>), of aphid species the Aphid Species File Database (<http://aphid.speciesfile.org>) and of ant species Antweb (<www.antweb.org>). Number Species Family Interact Figures ions Trees 1 Castanea henryi (Skan) Rehd. & Wils. Fagaceae 4 2 Castanopsis sclerophylla (Lindl. et Pax.) Fagaceae 14 Schott. 3 Choerospondias axillaris (Roxb.) Burtt & Hill Anacardiaceae 10 4 Cyclobalanopsis glauca (Thunb.) Oers. Fagaceae 7 5 Cyclobalanopsis myrsinaefolia Oerst. Fagaceae 3 6 Koelreuteria bipinnata Franch. Sapindaceae 1 7 Liquidambar formosana Hance Hamamelidaceae 4 8 Lithocarpus glaber (Thunb.) Nakai Fagaceae 4 9 Nyssa sinensis Oliver Nyssaceae 2 10 Quercus acutissima Carruth. Fagaceae 44 11 Quercus fabri Hance Fagaceae 28 1 12 Quercus serrata Murray Fagaceae 28 13 Rhus chinensis Mill. Anacardiaceae 17 14 Sapindus saponaria L. Sapindaceae 1 15 Schima superba Gardn. & Champ. Theaceae 27 Hemiptera 1 Aphis odinae (van der Goot, 1917) Aphididae 18 2 Aphis sp. CN01 Aphididae 2 3 Centrotinae Larvae 1 Membracidae 7 4 Centrotinae Larvae 2 Membracidae 1 5 Centrotinae sp. CN02 Membracidae 1 6 Centrotinae sp. CN03 Membracidae 4 7 Centrotinae sp. -
Crazy Ant (Paratrechina Sp
Midsouth Entomologist 3: 44–47 ISSN: 1936-6019 www.midsouthentomologist.org.msstate.edu Report The Invasive Rasberry Crazy Ant, Nylanderia sp. near pubens (Hymenoptera: Formicidae), Reported from Mississippi MacGown. J.1* and B. Layton1 Department of Entomology & Plant Pathology, Mississippi State University, Mississippi State, MS, 39762 *Corresponding Author: [email protected] Received: 18-XII-2009 Accepted: 23-XII-2009 Introduction The genus Nylanderia (Hymenoptera: Formicidae: Lasiini) currently includes 134 valid species and subspecies worldwide (LaPolla et al. 2010). Fifteen described species, including nine native and six introduced species, have been collected in the continental United States (Bolton et al. 2006, Trager 1984, Meyers 2008). Formerly, Nylanderia was considered to be a subgenus of Paratrechina and was only recently elevated to the generic level by LaPolla et al. (2010); consequently, it is referred to as Paratrechina in most of the literature. In 2002, large populations of an unknown Nylanderia species were discovered in Houston, Texas. After examination by taxonomic specialists, these ants were determined to be similar to Nylanderia pubens, the hairy crazy ant (Meyers 2008), known to occur in the Neotropical Region and in Florida (Wetterer and Keularts 2008), and similar to N. fulva (Mayr), which is native to South America (Meyers 2008). However, due to taxonomic uncertainty, this species has not been definitively identified as N. pubens, N. fulva or any of its eight subspecies, or even as an undescribed species. Therefore, at this time it is being identified as N. sp. near pubens (Meyers and Gold 2008), but it could also be referred to as N. sp. -
Hybridization in Ants
Rockefeller University Digital Commons @ RU Student Theses and Dissertations 2020 Hybridization in Ants Ian Butler Follow this and additional works at: https://digitalcommons.rockefeller.edu/ student_theses_and_dissertations Part of the Life Sciences Commons HYBRIDIZATION IN ANTS A Thesis Presented to the Faculty of The Rockefeller University in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy by Ian Butler June 2020 © Copyright by Ian Butler 2020 HYBRIDIZATION IN ANTS Ian Butler, Ph.D. The Rockefeller University 2020 Interspecific hybridization is a relatively common occurrence within all animal groups. Two main factors make hybridization act differently in ants than in other species: eusociality and haplodiploidy. These factors serve to reduce the costs of interspecific hybridization in ants while simultaneously allowing them to take advantage of certain benefits. Eusociality may mitigate the effects of hybridization by allowing hybrids to be shunted into the worker caste, potentially reducing the effects of hybrid sterility. In haplodiploid species, males do not have a father. They instead develop from unfertilized eggs as haploid clones of their mother. This means that interspecifically mated queens do not completely sacrifice reproductive potential even if all hybrids are sterile because they can still produce fertile males. These factors in turn suggest that hybridization should be more common among the social Hymenoptera than other animal groups. Nevertheless, current data suggest that ants hybridize at rates similar to other animal groups, although these data are limited. Furthermore, there is a large amount of overlap between cases of interspecific hybridization and cases of genetic caste determination. A majority of the cases in ants where caste is determined primarily by genotype are associated with hybridization. -
The Neotropical Species of the Ant Genus Strumigenys Fr
THE NEOTROPICAL SPECIES OF THE ANT GENUS STRUMIGENYS FR. SMITH: SYNOPSIS AND KEYS TO THE SPECIES BY WILLIAM L. BROWN, JR. Department ot Entomology, Cornell University Introduction The New World Strumiyenys have been revised through a series of twelve papers bearing the general foretitle, "The Neotropical species of the ant genus Strumigenys Ft. Smith," plus several articles by Dr. W. W. Kempf and by myself, beginning with my "Preliminary generic revision of the higher Dacetini" (Brown, 948). It now seems appro- priate to offer a unifying synopsis of the New World species of the genus, along with keys for identification and some general remarks. Species Synopsis of New World Strumigenys The synopsis below includes the names, each with author and date of publication, plus citation of the principal references in the Brown or Kempf papers already mentioned, which are listed in the section of "References" at the end of this article. These papers contain refer- ences to original descriptive and distributional material for each species, but I have included in the synopsis new or supplementary information wherever it seemed usetul to do so. The species are listed by groups in order of apparent relationship, as closely as it is possible to place them in a purely linear order. The probable relationships within the genus in the New World are discussed at the end of the synopsis. It will be noticed that the group placement of some species differs from that of the previous parts published. The present grouping represents a reconsideration of all of the New World species taken together.