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The Ants of Oklahoma Master of Science
THE ANTS OF OKLAHOMA By Jerry H. Young(I\" Bachelor of Science Oklahoma Agricultural and Mechanical College Stillwater, Oklahoma 1955 Submitted to the faculty of the Graduate School of the Oklahoma Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE January 1 1956 tl<lAWMA AGCMCl«.f�Al L �Ci'!AlttCAl e&U.Ull LIBRARY JUL16195 6 THE ANTS OF OKLAHOMA Thesis Approved: Thesis Adviser }>JcMem��f � 't'" he Thesis ) Committee Member of the Thesis Committee 7'4'.��Member of the Thesis Committee Head of the Department ifean of the Graduate School 361565 ii PREFACE The study of the distribution of ants in the United States has been a long and continuous process with many contributors, but the State of Oklahoma has not received the attentions of these observers to any great extent. The only known list of ants of Oklahoma is one prepared by Mo Ro Smith (1935)0 Early in 1954 a survey of the state of Oklahoma was made to determine the species present and their distributiono The results of this survey, which blanketed the entire State, are given in this paper. The author wishes to express his appreciation to Dro Do E. Howell, chairman of the writer's thesis committee, for his valuable assistance and careful guidance in the preparation of this papero Also, much guidance on preparation of this manuscrip_t was received from Drs. Do Eo Bryan, William H. Irwin and F. A. Fenton. Many of the determin ations were made by M. R. Smith.. Vital infonnation was obtained from the museums at Oklahoma Agricultural and Mechanical College and the University of Oklahoma. -
Check List 8(4): 722–730, 2012 © 2012 Check List and Authors Chec List ISSN 1809-127X (Available at Journal of Species Lists and Distribution
Check List 8(4): 722–730, 2012 © 2012 Check List and Authors Chec List ISSN 1809-127X (available at www.checklist.org.br) Journal of species lists and distribution Check list of ground-dwelling ants (Hymenoptera: PECIES S Formicidae) of the eastern Acre, Amazon, Brazil OF Patrícia Nakayama Miranda 1,2*, Marco Antônio Oliveira 3, Fabricio Beggiato Baccaro 4, Elder Ferreira ISTS 1 5,6 L Morato and Jacques Hubert Charles Delabie 1 Universidade Federal do Acre, Centro de Ciências Biológicas e da Natureza. BR 364 – Km 4 – Distrito Industrial. CEP 69915-900. Rio Branco, AC, Brazil. 2 Instituo Federal do Acre, Campus Rio Branco. Avenida Brasil 920, Bairro Xavier Maia. CEP 69903-062. Rio Branco, AC, Brazil. 3 Universidade Federal de Viçosa, Campus Florestal. Rodovia LMG 818, Km 6. CEP 35690-000. Florestal, MG, Brazil. 4 Instituto Nacional de Pesquisas da Amazônia, Programa de Pós-graduação em Ecologia. CP 478. CEP 69083-670. Manaus, AM, Brazil. 5 Comissão Executiva do Plano da Lavoura Cacaueira, Centro de Pesquisas do Cacau, Laboratório de Mirmecologia – CEPEC/CEPLAC. Caixa Postal 07. CEP 45600-970. Itabuna, BA, Brazil. 6 Universidade Estadual de Santa Cruz. CEP 45650-000. Ilhéus, BA, Brazil. * Corresponding author. E-mail: [email protected] Abstract: The ant fauna of state of Acre, Brazilian Amazon, is poorly known. The aim of this study was to compile the species sampled in different areas in the State of Acre. An inventory was carried out in pristine forest in the municipality of Xapuri. This list was complemented with the information of a previous inventory carried out in a forest fragment in the municipality of Senador Guiomard and with a list of species deposited at the Entomological Collection of National Institute of Amazonian Research– INPA. -
NEST STRUCTURE and FLIGHTS of the ANT Formica Obscuriventris Mayr
NEST STRUCTURE AND FLIGHTS OF THE ANT Formica obscuriventris Mayr BY MARY TALBOT The Edwin S. George Reserve, University of Michigan Nineteen colonies of Formica obscuriventris and Panicum sphaerocarpon Ell.) with scattered were discovered between 1951 and 1962 in the forbs (Verbascum thapsus L., Asclepias syriaca two square miles of the Edwin S . George Reserve L., Circium arvense (L.) Scop.). Oaks of the in southern Michigan. This paper describes flight nearby woods held a thick moist layer of fallen activities of males and females, atmospheric leaves, but on the sunny slope the leaves col- conditions which allowed or prevented flights lected abundantly only where held by logs and and the type of nest in which the winged ants their branches . developed and from which they flew. The matted leaf layers piled against the largest Nest Distribution and Structure log were used extensively for housing larvae and pupae. From here they could be moved Most of the 19 colonies were located at places readily to take advantage of fluctuating moisture where woods and fields met ; six were at woods' and heat. Brood was also found within the log, edges, three in small clearings, one at a fence row just under it, and in chambers extending down and two among small clumps of trees in fields. into the soil from 2 to 6 inches . At various Six were in a sandy strip between marsh and times brood was found under leaves along 30 woods, and one was on a ridge of an open oak- feet of the main log. Covered runways extended hickory wood . -
Akes an Ant an Ant? Are Insects, and Insects Are Arth Ropods: Invertebrates (Animals With
~ . r. workers will begin to produce eggs if the queen dies. Because ~ eggs are unfertilized, they usually develop into males (see the discus : ~ iaplodiploidy and the evolution of eusociality later in this chapter). =- cases, however, workers can produce new queens either from un ze eggs (parthenogenetically) or after mating with a male ant. -;c. ant colony will continue to grow in size and add workers, but at -: :;oint it becomes mature and will begin sexual reproduction by pro· . ~ -irgin queens and males. Many specie s produce males and repro 0 _ " females just before the nuptial flight . Others produce males and ---: : ._ tive fem ales that stay in the nest for a long time before the nuptial :- ~. Our largest carpenter ant, Camponotus herculeanus, produces males _ . -:= 'n queens in late summer. They are groomed and fed by workers :;' 0 it the fall and winter before they emerge from the colonies for their ;;. ights in the spring. Fin ally, some species, including Monomoriurn : .:5 and Myrmica rubra, have large colonies with multiple que ens that .~ ..ew colonies asexually by fragmenting the original colony. However, _ --' e polygynous (literally, many queens) and polydomous (literally, uses, referring to their many nests) ants eventually go through a -">O=- r' sexual reproduction in which males and new queens are produced. ~ :- . ant colony thus functions as a highly social, organ ized "super _ _ " 1." The queens and mo st workers are safely hidden below ground : : ~ - ed within the interstices of rotting wood. But for the ant workers ~ '_i S ' go out and forage for food for the colony,'life above ground is - =- . -
(Hymenoptera: Formicidae) by Diethe Ortius
A DOLICHODERUS TASCHENBERGI QUEEN FOUND IN A POLYGYNOUS COLONY OF D. PLAGIATUS (HYMENOPTERA: FORMICIDAE) BY DIETHE ORTIUS Theodor-Boveri-Institut LS ftir Verhaltensphysiologie und Soziobiologie Am Hubland, D-97074 Wtirzburg, Germany ABSTRACT Very little is known about colony founding strategies and social organization of the four North American species of the ant genus Dolichoderus. I here report the finding of a Dolichoderus taschen- bergi queen in a colony of D. plagiatus, which suggests parasitic colony founding may occur occasionally in Dolichoderus taschen- bergi. In addition, the colony contained three reproductively active queens of D. plagiatus, indicating that this species is facultatively polygynous. INTRODUCTION The ant genus Dolichoderus Lund is represented by four species in North America (Creighton, 1950): mariae Forel, plagiatus Mayr, pustulatus Mayr, and taschenbergi Mayr. Except for studies by Kannowski (1959, 1967) on the flight activities of these species and a review by Johnson (1989) of their distribution and nest sites, very little is known about the life histories of North American Dolichoderus. Several authors (Wheeler, 1905a; Cole, 1940; Carter, 1962a, b; Wheeler and Wheeler, 1963) have described below-ground nest structures and leaf litter nests for all four North American Dolichoderus. D. plagiatus is considered to be monogy- nous (Kannowski, 1967) and nuptial flights are known to occur between mid June and July (Kannowski, 1959). Among the 12 colonies censused by Kannowski (1967), one colony contained two queens, which, however, he did not dis- sect. The majority of the D. plagiatus colonies investigated by Manuscript received 4 March 1995. 147 148 Psyche [Vol. 102 Kannowski (1967) were monogynous, and the single polygynous colony found was interpreted as either a consequence of pleometrotic colony foundation (primary polygyny) or the adoption of young mated queens (secondary polygyny). -
Zootaxa, Crematogaster Pygmaea (Hymenoptera
Zootaxa 2075: 45–54 (2009) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2009 · Magnolia Press ISSN 1175-5334 (online edition) Crematogaster pygmaea (Hymenoptera: Formicidae: Myrmicinae), a highly polygynous and polydomous Crematogaster from northeastern Brazil YVES QUINET1, RACHID HAMIDI2, MARIO XAVIER RUIZ-GONZALEZ3, JEAN-CHRISTOPHE de BISEAU4 & JOHN T. LONGINO5 1Laboratório de Entomologia, Instituto Superior de Ciências Biomédicas, Universidade Estadual do Ceará, 60740-000 Fortaleza, Brazil; E-mail: [email protected] 2,4Servide d'Eco-Ethologie Evolutive CP 160/12, Université Libre de Bruxelles, 1050 Bruxelles, Belgium. E-mail: [email protected], [email protected], 3Laboratoire Evolution et Diversité Biologique, UMR-CNRS 5174, Université Paul Sabatier, 31062 Toulouse cedex 9, France. E-mail: [email protected] 5The Evergreen State College, Olympia, Washington 98505, USA. E-mail: [email protected] Abstract Crematogaster pygmaea is revived from synonymy under C. abstinens and newly characterized as a ground-nesting ant from northeastern Brazil. It is a habitat specialist in coastal and tabuleiro zones, where it forms extensive polydomous and polygynous colonies that nest in the soil. Workers forage extensively on honeydew and extrafloral nectar, and foraging continues day and night, although it is depressed at ground temperatures above 32°C. Gyne production occurs at the beginning of the rainy season, while male production starts in the dry season, some months before gyne production. Key words: Brazil, Ceará, Formicidae, Myrmicinae, Crematogaster, polygyny, polydomy Introduction The genus Crematogaster occurs throughout the tropical and subtropical regions of the world, and it is particularly diverse and abundant in the Neotropics. -
Fossil Ants (Hymenoptera: Formicidae): Ancient Diversity and the Rise of Modern Lineages
Myrmecological News 24 1-30 Vienna, March 2017 Fossil ants (Hymenoptera: Formicidae): ancient diversity and the rise of modern lineages Phillip BARDEN Abstract The ant fossil record is summarized with special reference to the earliest ants, first occurrences of modern lineages, and the utility of paleontological data in reconstructing evolutionary history. During the Cretaceous, from approximately 100 to 78 million years ago, only two species are definitively assignable to extant subfamilies – all putative crown group ants from this period are discussed. Among the earliest ants known are unexpectedly diverse and highly social stem- group lineages, however these stem ants do not persist into the Cenozoic. Following the Cretaceous-Paleogene boun- dary, all well preserved ants are assignable to crown Formicidae; the appearance of crown ants in the fossil record is summarized at the subfamilial and generic level. Generally, the taxonomic composition of Cenozoic ant fossil communi- ties mirrors Recent ecosystems with the "big four" subfamilies Dolichoderinae, Formicinae, Myrmicinae, and Ponerinae comprising most faunal abundance. As reviewed by other authors, ants increase in abundance dramatically from the Eocene through the Miocene. Proximate drivers relating to the "rise of the ants" are discussed, as the majority of this increase is due to a handful of highly dominant species. In addition, instances of congruence and conflict with molecular- based divergence estimates are noted, and distinct "ghost" lineages are interpreted. The ant fossil record is a valuable resource comparable to other groups with extensive fossil species: There are approximately as many described fossil ant species as there are fossil dinosaurs. The incorporation of paleontological data into neontological inquiries can only seek to improve the accuracy and scale of generated hypotheses. -
An Annotated List of the Ants (Hymenoptera: Formicidae) Found in Fort Washington and Piscataway National Parks, Maryland
AN ANNOTATED LIST OF THE ANTS (HYMENOPTERA: FORMICIDAE) FOUND IN FORT WASHINGTON AND PISCATAWAY NATIONAL PARKS, MARYLAND Theodore W. Suman Principal Investigator Theodore W. Suman, Ph.D. 7591 Polly's Hill Lane Easton, Maryland 21601 (410) 822 1204 [email protected] 'C ,:; ~) 71' 5 ?--- / I &, ·-1 U..~L:, 1 AN ANNOTATED LIST OF THE ANTS (HYMENOPTERA: FORMICIDAE) FOUNDINFORTWASHINGTONANDPISCATAWAYNATIONALPARKS, MARYLAND Theodore W. Suman The ants (Hymenoptera: Formicidae) listed in this report represent the results of a two-year (2002 - 2003) survey conducted in Fort Washington and Piscataway National Parks located in southwestern Prince Georges and northwestern Charles Counties, Maryland. This survey is part of the National Parks Service effort to broaden knowledge of the biodiversity occurring within the National Parks and was conducted under Permit # NACE-2002-SCI-0005 and Park-assigned Study Id. # NACE-00018. Table 1 is the result of this survey and consists of an alphabetical list (by subfamily, genus, and species) of all of the ant species found in both Parks. Information on the number of specimens collected, caste, date collected, and habitat is also included. Table 2 lists species found in only one or the other of the two Parks. General information on the collecting dates, collecting and extracting methods, and specific collecting sites is described below. COLLECTING DATES Collecting dates were spread throughout the spring to fall seasons of 2002 and 2003 to maximize the probability of finding all the species present. Collecting dates for each Park are listed separately. FORT WASHINGTON 2002 -27 March; 2,23 April; 20 May; 21,23 August; 12,25 September 2003 - 8 May; 12,26 June PISCATAWAY PARK 2002-9,16 April; 21 May; 24 June; 1 July 2003 - 20,30 May; 5 November 2 COLLECTING AND EXTRACTING METHODS Specimens were collected on site by the following methods. -
The University of Manitoba in Partial Fulfillment Of
SOME ANT-APHID ASSOCTATTONS IN MANITOBA I^TÏTH OBSERVATIONS ON INTERACTIONS BETI^IEEN Formica oreas comptula I^IIIEELER AND APHIDS AT BTRDS HTLL PARK, MANITOBA A Thesis Submitted to the Faculty of Graduate Studies The University of Manitoba by Mary Catherine Anne Madder In Partial Fulfillment of the Requirements for the Degree of Master of Science Department of Entomology October L978 f/,9R¡rnlçs SOMT ANT.APHID ASSÛCIATIt)NS IN MANÏTOBA I.IiTH OBSERVAT I(]NS CN INTTRACT IC)NS BET!,.ITEN Formica orç!q comp'bula l,lHETLER AND APHIDS AT BIRDS IIILL PARK, MANITOBA BY MARY CATHER.TNT ANNE il4ADDER A <lissertution submitted to the Faculty of Cra¿åuate Stuclies <¡f ttre Urriversity of Manitobu in partiir! fulfillment ol' tfue requirernents ol' tl¡e degrce of MASTER OF SCIENCT o" 1978 Fer¡nission hi¡s ber:¡r grurttcd to the LlllRAll'Y OF'TCI!: [JNIVUÈì- StTY OF MAN¡TO!ìA to lcnd or scll copies of tltås dissertatiol¡. to the NAT¡Ol"¿AL LIBRARY OF (IANADA to nlicrol'ilsn tltis rlissertatio¡r and tt¡ lend or sell cr.rpies of tl¡e filnl, und UNIVUIIStTV M!CIì,ûFILMS to publlsh at¡ ubstruct of this dissertation. The autltr¡r reserves other publieutit¡n rigfits, a¡ld neither tlte dissertation ¡ror extensivc cxtructs f rom it ntuy be printerJ or r-¡thcr- wise reproclucecl without thc autl¡or's writtctr irertttlssitltt. DEDÏCATIOT{ Dedicated to Gladys and Jimmie Carter of Corkery, Ontario (for all the happy summers) and to my Mother ]-I ACKNOI'TLEDGEMENTS r wish to express my gratitude to Dr. -
15 753 Hill 12.Indd
2010 SOUTHEASTERN NATURALIST 9(1):73–84 The Ant (Hymenoptera: Formicidae) Fauna of Black Belt Prairie Remnants in Alabama and Mississippi JoVonn G. Hill1,* and Richard L. Brown1 Abstract - Extensive areas of prairie were once found in the southeastern United States; however, in the last 200 years much of this habitat type has been destroyed. The largest of these prairie regions, the Black Belt Prairie, extends through por- tions of Alabama, Mississippi, and Tennessee. The ant fauna of these endangered grasslands has not been well documented; therefore, a survey was initiated, with collections made at 23 Black Belt Prairie remnants in Alabama and Mississippi dur- ing a four-year period. A total of 53 ant species, in six subfamilies and 25 genera were collected. Six exotic species were collected, and 11 species were found to be restricted to trees within the prairie, resulting in 36 species that likely represent the true prairie fauna. Introduction “In the fi elds the grass is short, no bush; the soil in places is a lead color, yel- low underneath, within the abode of the ants, and very stiff.” - Benjamin Hawkins (1938) on traveling through a Black Belt Prairie in Lowndes County, AL in 1798–99. Prior to European settlement, the southeastern United States had several regions dominated by grasslands or prairie (DeSelm and Murdock 1993, Peacock and Schauwecker 2003). One such region, called the “Black Belt,” extends in an arc from McNairy County, TN to Russell County, AL. Instead of being a continuous swath of open grassland, the historic landscape of the Black Belt was a heterogeneous landscape of prairies and several types of forest (see Barone 2005 for extensive references). -
Ant Diversity Studies in Acre
Bol. Mus. Para. Emílio Goeldi. Cienc. Nat., Belém, v. 15, n. 1, p. 113-134, jan.-abr. 2020 Ant diversity studies in Acre: what we know and what we could do to know more? Estudos de diversidade de formigas no Acre: o que sabemos e o que devemos fazer para saber mais? Fernando Augusto SchmidtI | Marília Maria Silva da CostaI, II | Felipe MartelloI | Amanda Batista de OliveiraIII | Andressa Silvana MenezesI | Luane Karoline FonteneleII | Elder Ferreira MoratoI | Marco Antônio OliveiraIV IUniversidade Federal do Acre. Rio Branco, Acre, Brasil IIUniversidade Federal de Lavras. Lavras, Minas Gerais, Brasil IIIUniversidade Federal do Amazonas. Manaus, Amazonas, Brasil IVUniversidade Federal de Viçosa. Florestal, Minais Gerais, Brasil Abstract: Brazil counts with one the largest ant diversity in the world. But, given its continental dimension and uneven scientific development process, there are still several gaps in the knowledge of this biodiversity. This fully applies to research on ant diversity in the state of Acre, southwestern Brazilian Amazon. Since 2014, in Acre, ants are being sampled by Rede BIA project, which aims to cover this gap. Thus, our main goal is to present the status of ant diversity studies in Acre regarding their progress and their contribution to the ant fauna knowledge, based on scientific papers and grey literature. We found 17 studies to Acre, which encompass a time range of 10 years, and a total of 338 species recorded. The studies are concentrated mainly in the southern and eastern parts of the state. Ground pitfall trap is the most used sampling technique. We point out that adding more sites to Rede BIA’s collecting efforts, plus focusing samplings in poorly studied habitats and ecosystems, especially in the western and eastern parts of the state will provide a lot of new data on ant species occurrence to Acre and to Brazil. -
The Ecology of Nest Movement in Social Insects
EN57CH15-McGlynn ARI 31 October 2011 8:2 The Ecology of Nest Movement in Social Insects Terrence P. McGlynn Department of Biology, California State University Dominguez Hills, Carson, California 90747; email: [email protected] Annu. Rev. Entomol. 2012. 57:291–308 Keywords First published online as a Review in Advance on absconding, ant, emigration, migration, nomadism, relocation September 9, 2011 The Annual Review of Entomology is online at Abstract ento.annualreviews.org Social insect colonies are typically mobile entities, moving nests from one This article’s doi: Annu. Rev. Entomol. 2012.57:291-308. Downloaded from www.annualreviews.org location to another throughout the life of a colony. The majority of social in- by California State University - Dominguez Hills on 12/13/11. For personal use only. 10.1146/annurev-ento-120710-100708 sect species—ants, bees, wasps, and termites—have likely adopted the habit Copyright c 2012 by Annual Reviews. ! of relocating nests periodically. The syndromes of nest relocation include All rights reserved legionary nomadism, unstable nesting, intrinsic nest relocation, and adven- 0066-4170/12/0107-0291$20.00 titious nest relocation. The emergence of nest movement is a functional response to a broad range of potential selective forces, including colony growth, competition, foraging efficiency, microclimate, nest deterioration, nest quality, parasitism, predation, and seasonality. Considering the great taxonomic and geographic distribution of nest movements, assumptions re- garding the nesting biology of social insects should be reevaluated, including our understanding of population genetics, life-history evolution, and the role of competition in structuring communities. 291 EN57CH15-McGlynn ARI 31 October 2011 8:2 INTRODUCTION It is a popular misconception that social insect colonies are sessile entities.