A New American Amblyopone, with Notes Foricide)
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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. -
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. -
American Museumnovitates
AMERICAN MUSEUM NOVITATES Published by Number 1079 THE AMERICAN MUSEum OF NATURAL HISTORY July 17, 1940 New York City A REVISION OF THE FORMS OF STIGMATOMMA PALLIPES BY WM. S. CREIGHTON Although the habits of Stigmatomma the North American representatives. The pallipes have been repeatedly studied range of oregonensis is strictly limited to none of these publications have been of the coastal region of the Pacific Northwest. much service to those who wish to deal Its nearest neighbor from a spatial stand- with the taxonomy of this interesting point appears to be the form described in species. This paper is an attempt to bring this paper as subterranea, which occurs in together and evaluate the scattered taxo- central Kansas. The Kansas variant is nomic publications which deal with S. scarcely less isolated from the eastern pallipes and its variants. Although ref- pallipes whose range does not seem to erences to this insect have repeatedly extend west of Michigan. As I shall show appeared in articles of a descriptive char- in a subsequent paragraph there is some acter there seems to be no adequate de- reason to believe that the ranges of the scription of the typical form. The ease variants are not as widely separated as our with which this insect may be recognized present scattered locality data would and the fact that it is our only species have indicate. Yet it is true that to the present fostered the notion that a thorough de- there are only two forms whose ranges are scription is not necessary. At one time adjacent. -
Hymenoptera, Formicidae: Amblyoponinae, Ectatomminae, Ponerinae) of Grube Messel, Germany: High Biodiversity in the Eocene G
Journal of Systematic Palaeontology, Vol. 10, Issue 4, December 2012, 725–753 The poneromorph ants (Hymenoptera, Formicidae: Amblyoponinae, Ectatomminae, Ponerinae) of Grube Messel, Germany: high biodiversity in the Eocene G. M. Dlusskya∗ and S. Wedmannb aDepartment of Evolution, Biological Faculty, M.V.Lomonosov Moscow State University, Vorobjovy gory, 119992, Moscow, Russia; bForschungsstation Grube Messel, Senckenberg Forschungsinstitut und Naturmuseum, Markstraße 35, D-64409, Messel, Germany (Received 17 September 2010; accepted 27 March 2011; printed 5 December 2012) Ants are a very successful group among insects, but the course of evolution of their biodiversity is still unclear. This study sheds light on ant diversification during the Eocene. Analysis of the ant taphocoenosis of the fossil site Grube Messel, Germany (47 Ma) yielded three poneromorph subfamilies and 22 new species in six genera, four of which are new: Pseudectatomma gen. nov., Cephalopone gen. nov., Cyrtopone gen. nov. and Messelepone gen. nov. Only one extant genus, Pachycondyla, is present in the taphocoenosis from Messel. The high diversity of poneromorph ants from Messel is very striking in comparison with middle to late Eocene European ambers. A significantly lower proportion of species in ambers can be assigned to poneromorph ants, and fewer poneromorph species are known from European ambers than from Messel. A possible gradual decline of the diversity of poneromorphs from the Eocene to the Miocene seems to be detectable worldwide. These insights are discussed in the context of the morphology and ecology of Poneromorpha and Formicomorpha. The proportion of ant castes in amber seems to indicate that already during the Eocene poneromorphs inhabited preferably litter and soil, whereas formicomorphs preferred the arboreal realm. -
Notes on the Biology of the Oriental Amblyoponine Ant Myopopone Castanea: Queen-Worker Dimorphism, Worker Polymorphism and Larval Hemolymph Feeding by Workers
Entomological Science (2010) 13, 199–204 doi:10.1111/j.1479-8298.2010.00384.x ORIGINAL ARTICLE Notes on the biology of the Oriental amblyoponine ant Myopopone castanea: Queen-worker dimorphism, worker polymorphism and larval hemolymph feeding by workers (Hymenoptera: Formicidae)ens_384 199..204 Fuminori ITO Faculty of Agriculture, Kagawa University, Miki, Kagawa, Japan Abstract Queen-worker dimorphism, worker polymorphism and worker behavior in the Oriental amblyoponine ant Myopopone castanea were studied. Queen body size was large (head width, 3.0 mm) with 24 to 32 ovarioles while workers showed a remarkable size variation in both body size (head width 1.48 to 2.18 mm) and ovariole number (6 to 22). Both head width and abdomen width showed allometric growth against thorax width. Workers performed larval hemolymph feeding as was described for Amblyopone silvestrii queens. Key words: Amblyoponinae, ant, caste dimorphism, Hymenoptera, Myopopone. INTRODUCTION its distribution is limited to tropical forests in the Oriental tropics to northernmost Australia, and it is not The ant subfamily Amblyoponinae has been regarded as a common species (Brown 1960). In this paper, I give one of the early branching lineages among family For- information on the biology of Myopopone castanea micidae (e.g. Brown 1960; Wilson 1971). Their broad (Smith) observed in West Sumatra, Indonesia, and attachment between petiole and the third segment of Sabah, Borneo. The biological information mentioned abdomen has been considered as an ancestral character. here is fragmentary; however, it is valuable for under- Even though the character status and the phylogenetic standing the diversity of the subfamily Amblyoponinae. position is still controversial (e.g. -
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. -
(Insecta: Hymenoptera), Part II—Cerapachyinae, Aenictinae, Dorylinae, Leptanillinae, Amblyoponinae, Ponerinae, Ectatomminae and Proceratiinae
Zootaxa 3860 (1): 001–046 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2014 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3860.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:FDFD1014-8DDA-4EED-A385-95FA4F964CFC Generic Synopsis of the Formicidae of Vietnam (Insecta: Hymenoptera), Part II—Cerapachyinae, Aenictinae, Dorylinae, Leptanillinae, Amblyoponinae, Ponerinae, Ectatomminae and Proceratiinae KATSUYUKI EGUCHI1,4, BUI TUAN VIET2 & SEIKI YAMANE3 1Department of Biological Sciences, Graduate School of Science and Engineering, Tokyo Metropolitan University, Tokyo, 192-0397, Japan 2Vietnam National Museum of Nature, 18 Hoang Quoc Viet, Cau Giay, Ha Noi, Vietnam 3Haruyama-cho 1054-1, Kagoshima-shi, 899-2704, Japan 4Corresponding author. E-mail: [email protected] / [email protected] Abstract Of the subfamilies and genera known from Vietnam, the following taxa are treated in this second part of the series entitled “Generic Synopsis of the Formicidae of Vietnam”: CERAPACHYINAE: Cerapachys, Simopone; AENICTINAE: Aenic- tus; DORYLINAE: Dorylus; LEPTANILLINAE: Leptanilla, Protanilla; AMBLYOPONINAE: Myopopone, Mystrium, Opamyrma, Prionopelta, Stigmatomma; PONERINAE: Anochetus, Brachyponera, Buniapone, Centromyrmex, Crypto- pone, Diacamma, Ectomomyrmex, Euponera, Harpegnathos, Hypoponera, Leptogenys, Mesoponera, Odontomachus, Odontoponera, Parvaponera, Platythyrea, Ponera, Pseudoneoponera; ECTATOMMINAE: Gnamptogenys; PROCER- ATIINAE: Discothyrea, Probolomyrmex, Proceratium. For each of these subfamilies we provide keys to genera (when there is more than one genus) known from Vietnam. For each genus we provide a synopsis and a list of Vietnamese species. Key words: dorylomorph, leptanillomorph, poneromorph, Indo-China, key Introduction This is the second part of the series entitled “Generic Synopsis of the Formicidae of Vietnam”. The first part covers Myrmicinae and Pseudomyrmicinae (Eguchi et al. -
Phylogeny and Biogeography of a Hyperdiverse Ant Clade (Hymenoptera: Formicidae)
UC Davis UC Davis Previously Published Works Title The evolution of myrmicine ants: Phylogeny and biogeography of a hyperdiverse ant clade (Hymenoptera: Formicidae) Permalink https://escholarship.org/uc/item/2tc8r8w8 Journal Systematic Entomology, 40(1) ISSN 0307-6970 Authors Ward, PS Brady, SG Fisher, BL et al. Publication Date 2015 DOI 10.1111/syen.12090 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Systematic Entomology (2015), 40, 61–81 DOI: 10.1111/syen.12090 The evolution of myrmicine ants: phylogeny and biogeography of a hyperdiverse ant clade (Hymenoptera: Formicidae) PHILIP S. WARD1, SEÁN G. BRADY2, BRIAN L. FISHER3 andTED R. SCHULTZ2 1Department of Entomology and Nematology, University of California, Davis, CA, U.S.A., 2Department of Entomology, National Museum of Natural History, Smithsonian Institution, Washington, DC, U.S.A. and 3Department of Entomology, California Academy of Sciences, San Francisco, CA, U.S.A. Abstract. This study investigates the evolutionary history of a hyperdiverse clade, the ant subfamily Myrmicinae (Hymenoptera: Formicidae), based on analyses of a data matrix comprising 251 species and 11 nuclear gene fragments. Under both maximum likelihood and Bayesian methods of inference, we recover a robust phylogeny that reveals six major clades of Myrmicinae, here treated as newly defined tribes and occur- ring as a pectinate series: Myrmicini, Pogonomyrmecini trib.n., Stenammini, Solenop- sidini, Attini and Crematogastrini. Because we condense the former 25 myrmicine tribes into a new six-tribe scheme, membership in some tribes is now notably different, espe- cially regarding Attini. We demonstrate that the monotypic genus Ankylomyrma is nei- ther in the Myrmicinae nor even a member of the more inclusive formicoid clade – rather it is a poneroid ant, sister to the genus Tatuidris (Agroecomyrmecinae). -
1 the RESTRUCTURING of ARTHROPOD TROPHIC RELATIONSHIPS in RESPONSE to PLANT INVASION by Adam B. Mitchell a Dissertation Submitt
THE RESTRUCTURING OF ARTHROPOD TROPHIC RELATIONSHIPS IN RESPONSE TO PLANT INVASION by Adam B. Mitchell 1 A dissertation submitted to the Faculty of the University of Delaware in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Entomology and Wildlife Ecology Winter 2019 © Adam B. Mitchell All Rights Reserved THE RESTRUCTURING OF ARTHROPOD TROPHIC RELATIONSHIPS IN RESPONSE TO PLANT INVASION by Adam B. Mitchell Approved: ______________________________________________________ Jacob L. Bowman, Ph.D. Chair of the Department of Entomology and Wildlife Ecology Approved: ______________________________________________________ Mark W. Rieger, Ph.D. Dean of the College of Agriculture and Natural Resources Approved: ______________________________________________________ Douglas J. Doren, Ph.D. Interim Vice Provost for Graduate and Professional Education I certify that I have read this dissertation and that in my opinion it meets the academic and professional standard required by the University as a dissertation for the degree of Doctor of Philosophy. Signed: ______________________________________________________ Douglas W. Tallamy, Ph.D. Professor in charge of dissertation I certify that I have read this dissertation and that in my opinion it meets the academic and professional standard required by the University as a dissertation for the degree of Doctor of Philosophy. Signed: ______________________________________________________ Charles R. Bartlett, Ph.D. Member of dissertation committee I certify that I have read this dissertation and that in my opinion it meets the academic and professional standard required by the University as a dissertation for the degree of Doctor of Philosophy. Signed: ______________________________________________________ Jeffery J. Buler, Ph.D. Member of dissertation committee I certify that I have read this dissertation and that in my opinion it meets the academic and professional standard required by the University as a dissertation for the degree of Doctor of Philosophy. -
Trophallaxis: 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 (Hymeno ptera: 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. -
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Myrmecological News 21 Digital supplementary material Digital supplementary material to PEETERS , C. & ITO , F. 2015: Wingless and dwarf workers underlie the ecological suc- cess of ants (Hymenoptera: Formicidae) . – Myrmecological News 21: 117-130. Appendix S1. List of 286 ant genera in which head width of workers was measured (maximum width of head capsule excluding eyes, in full-face view), as well as 21 eusocial bees and 25 eusocial wasps for which data were obtained in the literature. Species for which results are not indicated have worker heads wider than 1 mm, i.e., there are no "dwarf" workers. All data are summarized in Fig. 2. * measured from photographs available on www.antweb.org FORMICIDAE Aenictus sp. < 0.5 mm (see BOLTON 2015) Asphinctanilloides amazona* < 0.5 mm Cerapachys sp. < 0.5 mm Agroecomyrmecinae Cylindromyrmex brevitarsus* < 1 mm Ankylomyrma coronacantha* Dorylus laevigatus < 1 mm Tatuidris tatusia* Eciton sp. Labidus spininodis* < 1 mm Amblyoponinae Leptanilloides biconstricta* < 0.5 mm Adetomyrma caputleae* < 1 mm Neivamyrmex sp. cr01 * < 0.5 mm Amblyopone australis < 1 mm Nomamyrmex esenbeckii* < 1 mm Apomyrma stygia* < 0.5 mm Simopone occulta* < 1 mm Bannapone scrobiceps* < 1 mm Sphinctomyrmex cribratus* < 0.5 mm Concoctio concenta* < 0.5 mm Tanipone aversa* < 1 mm Myopopone castanea Vicinopone conciliatrix* < 0.5 mm Mystrium camillae < 0.5 mm Onychomyrmex hedleyi < 0.5 mm Ectatomminae Opamyrma hungvuong* < 0.5 mm Ectatomma sp. Prionopelta kraepelini < 0.5 mm Gnamptogenys cribrata < 1 mm Stigmatomma besucheti* < 0.5 mm Rhytidoponera sp. < 1 mm Xymmer sp. mg03 * < 0.5 mm Typhlomyrmex pusillus* < 0.5 mm Aneuretinae Formicinae Aneuretus simoni* < 0.5 mm Acanthomyops sp. -
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Myrmecological News 20 Digital supplementary material Digital supplementary material to LANAN, M. 2014: Spatiotemporal resource distribution and foraging strategies of ants (Hymenoptera: Formicidae). – Myrmecological News 20: 53-70. Tab. S1: Data and citations for information presented in Figure 3 and Figure S1. Note that no data in any column indi- cates a lack of reports in the literature. For instance, no data in the column for nesting strategy should not be interpreted as a positive report of strict monodomy, and ants may collect foods that have not been reported. Species Resource collected Foraging strategy Nesting strategy Acanthognathus rudis Small prey: collembola Solitary foraging (GRONENBERG & al. 1998) (GRONENBERG & al. 1998) Acromyrmex ambiguus Leaves (FOWLER 1985, Trunk trails, partially subterranean (FOWLER SAVERSCHEK & ROCES 2011) 1985) trails (SAVERSCHEK & ROCES 2011) Acromyrmex balzani Grass (LOPES & al. 2004) Recruitment, type = ? (LOPES & al. 2004) Polydomy (ICHINOSE Solitary foraging (PODEROSO & al. 2009) & al. 2006) Solitary foraging (FOWLER 1985) Acromyrmex coronatus Leaves (WETTERER 1995) Trunk trails (WETTERER 1995) Acromyrmex crassispinus Leaves (FOWLER 1985) Two to five trunk trails (FOWLER 1985) Acromyrmex disciger Leaves (FOWLER 1985) Trunk trails (FOWLER 1985) Acromyrmex fracticornis Grass (FOWLER & ROBINSON 1977) Solitary (FOWLER & ROBINSON 1977) Acromyrmex heyeri Grass (BOLLAZZI & ROCES 2011) Trunk trails (FOWLER 1985, BOLLAZZI & ROCES 2011) Acromyrmex hispidus fallax Leaves (FOWLER 1985) Trunk trails (FOWLER 1985) Acromyrmex laticeps Leaves (FOWLER 1985) Trunk trails (FOWLER 1985) Acromyrmex lobicornis Leaves (ELIZALDE & FARJI-BERNER Trunk trails (ELIZALDE & FARJI-BERNER 2012) 2012) Acromyrmex lundii Leaves (FOWLER 1988), mush- Trunk trails (FOWLER 1988) rooms (LECHNER & JOSENS 2012) Acromyrmex niger Leaves (SOUSA-SOUTO & al. 2005) Trunk trails (SOUSA-SOUTO & al.