Ant Communities of Florida's Upland Ecosystems

Total Page:16

File Type:pdf, Size:1020Kb

Ant Communities of Florida's Upland Ecosystems ANT COMMUNITIES OF FLORIDA’S UPLAND ECOSYSTEMS: ECOLOGY AND SAMPLING By JOSHUA R. KING A DISSERTATION PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY UNIVERSITY OF FLORIDA 2004 Copyright 2004 by Joshua R. King To my wife. Thank you for teaching me what is truly important in life. ACKNOWLEDGMENTS I would like to thank my committee members John Capinera, Mark Deyrup, Robert McSorley, Sanford Porter, and Kenneth Portier for reading the dissertation and providing sound advice on the politics of academia, statistics, publishing, teaching, and the pursuit of biological knowledge. Their contributions have all aided in my development as a scientist, collaborator, and colleague; for that I am grateful. In particular I would like to thank my advisor, Sanford Porter. None of this work could have been accomplished without the support, laboratory space, equipment, and encouragement he provided. I am grateful to Lloyd Davis for teaching me to be a better collector and observer of the natural world. A man who has forgotten more entomology than I will ever know, he has impressed on me that a broad entomological knowledge is the best context within which to build an understanding of ants. I am indebted to Mark Deyrup for showing me that it is possible to know how to identify everything, and that I must not forget that sampling and theory can never replace collecting and natural history. Thanks go to Lloyd Morrison for sharing ideas, insight on being a better scientist, surfing, and Frisbee. I thank Sanford Porter and Walter Tschinkel for sharing ideas and showing me the importance of a mechanistic, experimental approach to studying ants. I also thank Walter Tschinkel and his lab group for sharing ideas and being patient while I finished. I thank Lloyd Davis and Mark Deyrup for assisting with and verifying species identifications. I am also grateful for myrmecological advice from Stefan Cover, without iv which the project would not have been as successful. I thank the Archbold Biological Station and Mark Deyrup for laboratory space and accommodation during part of this work. I thank the University of Florida, the Florida Department of Environmental Protection’s State Parks Division, and the U.S. National Forest Service for permission to perform sampling in the Katherine Ordway Biological Preserve, San Felasco Hammock State Park, and Osceola National Forest, respectively. Voucher specimens from this project have been donated to Harvard’s Museum of Comparative Zoology and the Archbold Biological Station. I thank the University of Florida for financial support during part of my graduate studies in the form of a University of Florida Alumni Fellowship. I also thank Walter Tschinkel for financial support during the completion of the dissertation. I sincerely thank my mother, Pamela Snow, for instilling in me a love of scholarship, the natural world, and writing. I am also indebted to her for teaching me patience and the desire to always be optimistic and forward-moving, no matter how rough the going gets or how daunting the task. I am indebted to my wife, Kari, for teaching me to be more disciplined. I am also grateful to my wife for emotional support and for sharing her life with me. Without these things I would not have been able to complete the dissertation. Finally, I thank my daughter Maizie for showing me what a joy life can be. v TABLE OF CONTENTS page ACKNOWLEDGMENTS ................................................................................................. iv LIST OF TABLES........................................................................................................... viii LIST OF FIGURES ........................................................................................................... ix ABSTRACT.........................................................................................................................x CHAPTER 1 INTRODUCTION ........................................................................................................1 2 ASSEMBLY RULES FOR INSECTS AT LOCAL AND REGIONAL SCALES: ABUNDANCE, DIVERSITY, AND BIOMASS OF ANTS IN FLORIDA’S UPLAND ECOSYTEMS .............................................................................................4 Introduction...................................................................................................................4 Study Area and Methods ..............................................................................................8 Upland Ecosystems ...............................................................................................8 Inventory Design .................................................................................................12 Analysis ...............................................................................................................14 Results.........................................................................................................................22 Species Richness .................................................................................................22 Abundance and Biomass .....................................................................................22 Behavioral Dominance ........................................................................................27 Species Co-occurrence ........................................................................................28 Introduced Species...............................................................................................29 Discussion...................................................................................................................30 Taxocene Attributes.............................................................................................30 Biogeography, Synthesis, and Applications........................................................50 3 EVALUATION OF SAMPLING METHODS AND SPECIES RICHNESS ESTIMATORS FOR ANTS IN UPLAND ECOSYSTEMS IN FLORIDA..............78 Introduction.................................................................................................................78 Methods ......................................................................................................................83 Study Area...........................................................................................................83 Sampling..............................................................................................................83 vi Analysis ...............................................................................................................85 Results.........................................................................................................................90 Observed and Estimated Species Richness .........................................................90 Rarity ...................................................................................................................92 Complementarity of Ecosystems.........................................................................92 Effectiveness of Sampling Methods....................................................................93 Discussion...................................................................................................................95 Inventory Completeness ......................................................................................95 Performance of Species Richness Estimators......................................................97 Rarity ...................................................................................................................98 Efficiency of Sampling Methods.......................................................................100 4 CONCLUSION.........................................................................................................113 LIST OF REFERENCES.................................................................................................116 BIOGRAPHICAL SKETCH ...........................................................................................132 vii LIST OF TABLES Table page 2-1 Species list ................................................................................................................59 2-2 Species richness, slope (m), and R2 values for fitted lines .......................................63 2-3 Five most abundant species ......................................................................................64 2-4 Co-occurrence patterns of ants .................................................................................65 2-5 Body size overlap patterns of ants............................................................................66 2-6 Ant species turnover .................................................................................................67 3-1 Species richness estimates and measures of inventory completeness ....................105 3-2 Mean percent faunal complementarity among ecosystems ....................................106 3-3 Percent faunal complementarity of sample methods..............................................107 viii LIST OF FIGURES Figure page 2-1 Map of Florida..........................................................................................................68 2-2 Rarefaction curves for ecosystems ...........................................................................69 2-3 Relationship between species occurrences and body
Recommended publications
  • Insect Ecology-An Ecosystem Approach
    FM-P088772.qxd 1/24/06 11:11 AM Page xi PREFACE his second edition provides an updated and expanded synthesis of feedbacks and interactions between insects and their environment. A number of recent studies have T advanced understanding of feedbacks or provided useful examples of principles. Mo- lecular methods have provided new tools for addressing dispersal and interactions among organisms and have clarified mechanisms of feedback between insect effects on, and responses to, environmental changes. Recent studies of factors controlling energy and nutri- ent fluxes have advanced understanding and prediction of interactions among organisms and abiotic nutrient pools. The traditional focus of insect ecology has provided valuable examples of adaptation to environmental conditions and evolution of interactions with other organisms. By contrast, research at the ecosystem level in the last 3 decades has addressed the integral role of her- bivores and detritivores in shaping ecosystem conditions and contributing to energy and matter fluxes that influence global processes. This text is intended to provide a modern per- spective of insect ecology that integrates these two traditions to approach the study of insect adaptations from an ecosystem context. This integration substantially broadens the scope of insect ecology and contributes to prediction and resolution of the effects of current envi- ronmental changes as these affect and are affected by insects. This text demonstrates how evolutionary and ecosystem approaches complement each other, and is intended to stimulate further integration of these approaches in experiments that address insect roles in ecosystems. Both approaches are necessary to understand and predict the consequences of environmental changes, including anthropogenic changes, for insects and their contributions to ecosystem structure and processes (such as primary pro- ductivity, biogeochemical cycling, carbon flux, and community dynamics).
    [Show full text]
  • Ecological Importance of Insects in Selenium Biogenic Cycling
    Hindawi Publishing Corporation International Journal of Ecology Volume 2014, Article ID 835636, 6 pages http://dx.doi.org/10.1155/2014/835636 Review Article Ecological Importance of Insects in Selenium Biogenic Cycling Nadezhda Golubkina,1 Sergey Sheshnitsan,2 and Marina Kapitalchuk2 1 Agrochemical Research Center, All-Russian Scientific Research Institute of Vegetable Breeding and Seeds Production, Russian Academy of Agricultural Sciences, Moscow 143080, Russia 2 Department of Natural Sciences and Geography, Pridnestrovian State University, 3300 Tiraspol, Moldova Correspondence should be addressed to Nadezhda Golubkina; [email protected] Received 23 July 2013; Accepted 30 December 2013; Published 6 February 2014 Academic Editor: Jean-Guy Godin Copyright © 2014 Nadezhda Golubkina et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Selenium is an essential trace element for animal and human beings. Despite the importance of insects in most ecosystems and their significant contribution to the biological cycling of trace elements due to high abundance, population productivity, and diverse ecosystem functions, surprisingly little information is available on selenium bioaccumulation by these arthropods. This review considers selenium essentiality and toxicity to insects as well as insects’ contribution to selenium trophic transfer through the food chains. Data on Se accumulation by insects of the Dniester River Valley with no anthropogenic Se loading reveal typically low Se content in necrophagous insects compared to predators and herbivores and seasonal variations in Se accumulation. 1. Introduction This brief review considers selenium essentiality and toxicity to insects as well as insects’ contribution to selenium Selenium (Se) essentiality in vertebrates has been proven in trophic transfer through the food chains.
    [Show full text]
  • Ecology of Forest Insect Invasions
    Biol Invasions (2017) 19:3141–3159 DOI 10.1007/s10530-017-1514-1 FOREST INVASION Ecology of forest insect invasions E. G. Brockerhoff . A. M. Liebhold Received: 13 March 2017 / Accepted: 14 July 2017 / Published online: 20 July 2017 Ó Springer International Publishing AG 2017 Abstract Forests in virtually all regions of the world trade. The dominant invasion ‘pathways’ are live plant are being affected by invasions of non-native insects. imports, shipment of solid wood packaging material, We conducted an in-depth review of the traits of ‘‘hitchhiking’’ on inanimate objects, and intentional successful invasive forest insects and the ecological introductions of biological control agents. Invading processes involved in insect invasions across the insects exhibit a variety of life histories and include universal invasion phases (transport and arrival, herbivores, detritivores, predators and parasitoids. establishment, spread and impacts). Most forest insect Herbivores are considered the most damaging and invasions are accidental consequences of international include wood-borers, sap-feeders, foliage-feeders and seed eaters. Most non-native herbivorous forest insects apparently cause little noticeable damage but some species have profoundly altered the composition and ecological functioning of forests. In some cases, Guest Editors: Andrew Liebhold, Eckehard Brockerhoff and non-native herbivorous insects have virtually elimi- Martin Nun˜ez / Special issue on Biological Invasions in Forests nated their hosts, resulting in major changes in forest prepared by a task force of the International Union of Forest composition and ecosystem processes. Invasive preda- Research Organizations (IUFRO). tors (e.g., wasps and ants) can have major effects on forest communities. Some parasitoids have caused the Electronic supplementary material The online version of this article (doi:10.1007/s10530-017-1514-1) contains supple- decline of native hosts.
    [Show full text]
  • Food Quality, Competition, and Parasitism Influence Feeding Preference in a Neotropical Lepidopteran
    Ecology, 87(12), 2006, pp. 3058–3069 Ó 2006 by the Ecological Society of America FOOD QUALITY, COMPETITION, AND PARASITISM INFLUENCE FEEDING PREFERENCE IN A NEOTROPICAL LEPIDOPTERAN 1,2,3 2 2 1,2 THOMAS A. KURSAR, BRETT T. WOLFE, MARY JANE EPPS, AND PHYLLIS D. COLEY 1Department of Biology, University of Utah, Salt Lake City, Utah 84112 USA 2Smithsonian Tropical Research Institute, Balboa, Panama Abstract. We surveyed Lepidoptera found on 11 species of Inga (Fabaceae:Mimosoideae) co-existing on Barro Colorado Island, Panama, to evaluate factors influencing diet choice. Of the 47 species of caterpillars (747 individuals) recorded, each fed on a distinct set of Inga.In the field, 96% of the individuals were found on young leaves. Growth rates of caterpillars that were fed leaves in the laboratory were 60% higher on young leaves compared to mature leaves. When caterpillars were fed leaves of nonhost Inga, they grew more slowly. These data provide support for a link between preference and performance. However, among hosts on which larvae normally occurred, faster growth rates were not associated with greater host electivity (the proportion of larvae found on each host species in the field, corrected for host abundance). Growth rates on normal hosts were positively correlated with leaf expansion rates of the host, and fast expansion was associated with leaves with higher nutritional content. Detailed studies on a gelechiid leaf roller, the species with the largest diet breadth, allowed us to assess the importance of factors other than growth that could influence diet electivity. This species showed a 1.7-fold difference in growth rate among Inga hosts and faster growth on species with fast-expanding leaves.
    [Show full text]
  • Arkansas Academy of Science
    Journal of the CODEN: AKASO ISBN: 0097-4374 ARKANSAS ACADEMY OF SCIENCE VOLUME 61 2007 Library Rate ARKANSAS ACADEMY OF SCIENCE ARKANSAS TECH UNIVERSITY DEPARTMENT OF PHYSICAL SCIENCES 1701 N. BOULDER RUSSELLVILLE. AR 72801-2222 Arkansas Academy ofScience, Dept. of Physical Sciences, Arkansas Tech University PAST PRESIDENTS OF THE ARKANSAS ACADEMY OF SCIENCE Charles Brookover, 1917 C. E. Hoffman, 1959 Paul Sharrah, 1984 Dwight M. Moore, 1932-33, 64 N. D. Buffaloe, 1960 William L. Evans, 1985 Flora Haas, 1934 H. L. Bogan, 1961 Gary Heidt, 1986 H. H. Hyman, 1935 Trumann McEver, 1962 Edmond Bacon, 1987 L. B. Ham, 1936 Robert Shideler, 1963 Gary Tucker, 1988 W. C. Muon, 1937 L. F. Bailey, 1965 David Chittenden, 1989 M. J. McHenry, 1938 James H. Fribourgh, 1966 Richard K. Speairs, Jr. 1990 T. L. Smith, 1939 Howard Moore, 1967 Robert Watson, 1991 P. G. Horton, 1940 John J. Chapman, 1968 Michael W. Rapp, 1992 I. A. Willis, 1941-42 Arthur Fry, 1969 Arthur A. Johnson, 1993 L. B. Roberts, 1943-44 M. L. Lawson, 1970 George Harp, 1994 JeffBanks, 1945 R. T. Kirkwood, 1971 James Peck, 1995 H. L. Winburn, 1946-47 George E. Templeton, 1972 Peggy R. Dorris, 1996 E. A. Provine, 1948 E. B. Wittlake, 1973 Richard Kluender, 1997 G. V. Robinette, 1949 Clark McCarty, 1974 James Daly, 1998 John R. Totter, 1950 Edward Dale, 1975 Rose McConnell, 1999 R. H. Austin, 1951 Joe Guenter, 1976 Mostafa Hemmati, 2000 E. A. Spessard, 1952 Jewel Moore, 1977 Mark Draganjac, 2001 Delbert Swartz, 1953 Joe Nix, 1978 John Rickett, 2002 Z.
    [Show full text]
  • Sistemática Y Ecología De Las Hormigas Predadoras (Formicidae: Ponerinae) De La Argentina
    UNIVERSIDAD DE BUENOS AIRES Facultad de Ciencias Exactas y Naturales Sistemática y ecología de las hormigas predadoras (Formicidae: Ponerinae) de la Argentina Tesis presentada para optar al título de Doctor de la Universidad de Buenos Aires en el área CIENCIAS BIOLÓGICAS PRISCILA ELENA HANISCH Directores de tesis: Dr. Andrew Suarez y Dr. Pablo L. Tubaro Consejero de estudios: Dr. Daniel Roccatagliata Lugar de trabajo: División de Ornitología, Museo Argentino de Ciencias Naturales “Bernardino Rivadavia” Buenos Aires, Marzo 2018 Fecha de defensa: 27 de Marzo de 2018 Sistemática y ecología de las hormigas predadoras (Formicidae: Ponerinae) de la Argentina Resumen Las hormigas son uno de los grupos de insectos más abundantes en los ecosistemas terrestres, siendo sus actividades, muy importantes para el ecosistema. En esta tesis se estudiaron de forma integral la sistemática y ecología de una subfamilia de hormigas, las ponerinas. Esta subfamilia predomina en regiones tropicales y neotropicales, estando presente en Argentina desde el norte hasta la provincia de Buenos Aires. Se utilizó un enfoque integrador, combinando análisis genéticos con morfológicos para estudiar su diversidad, en combinación con estudios ecológicos y comportamentales para estudiar la dominancia, estructura de la comunidad y posición trófica de las Ponerinas. Los resultados sugieren que la diversidad es más alta de lo que se creía, tanto por que se encontraron nuevos registros durante la colecta de nuevo material, como porque nuestros análisis sugieren la presencia de especies crípticas. Adicionalmente, demostramos que en el PN Iguazú, dos ponerinas: Dinoponera australis y Pachycondyla striata son componentes dominantes en la comunidad de hormigas. Análisis de isótopos estables revelaron que la mayoría de las Ponerinas ocupan niveles tróficos altos, con excepción de algunas especies arborícolas del género Neoponera que dependerían de néctar u otros recursos vegetales.
    [Show full text]
  • Florida Urban Forestry Council 2017 Issue Four
    CouncilThe Quarterly Quarterly Newsletter of the Florida Urban Forestry Council 2017 Issue Four The Council Quarterly newsletter is published quarterly by the Florida Urban Forestry Council and is intended as an educational benefit to our members. Information may be reprinted if credit is given to the author(s) and this newsletter. All pictures, articles, advertisements, and other data are in no way to be construed as an endorsement of the author, products, services, or techniques. Likewise, the statements and opinions expressed herein are those of the individual authors and do not represent the view of the Florida Urban Forestry Council or its Executive Committee. This newsletter is made possible by the generous support of the Florida Department of Agriculture and Consumer Services, Florida Forest Service, Adam H. Putnam Commissioner. ADAPTIVE URBAN FOREST MANAGEMENT AND CATASTROPHIC WEATHER EVENTS: A CASE STUDY FROM EUGENE, OREGON Submitted by Scott Altenhoff and Eric Cariaga, City of Eugene, Oregon It seems our “new normal” is far There is, however, an upside to this story. and improvements through the frequent from normal; it’s time to expect the We have learned how to better address feedback. In the lines to follow, we’ll briefly catastrophic events. We use to plan and share the story of how Eugene made the unexpected and to do our best in base our work by looking back at past shift towards AM and how this shift made preparing for an uncertain future. models and tendencies. Now we practice a positive difference in both our storm a forward-looking approach. This new response and our overall operations.
    [Show full text]
  • 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.
    [Show full text]
  • Poneromorfas Do Brasil Miolo.Indd
    10 - Citogenética e evolução do cariótipo em formigas poneromorfas Cléa S. F. Mariano Igor S. Santos Janisete Gomes da Silva Marco Antonio Costa Silvia das Graças Pompolo SciELO Books / SciELO Livros / SciELO Libros MARIANO, CSF., et al. Citogenética e evolução do cariótipo em formigas poneromorfas. In: DELABIE, JHC., et al., orgs. As formigas poneromorfas do Brasil [online]. Ilhéus, BA: Editus, 2015, pp. 103-125. ISBN 978-85-7455-441-9. Available from SciELO Books <http://books.scielo.org>. All the contents of this work, except where otherwise noted, is licensed under a Creative Commons Attribution 4.0 International license. Todo o conteúdo deste trabalho, exceto quando houver ressalva, é publicado sob a licença Creative Commons Atribição 4.0. Todo el contenido de esta obra, excepto donde se indique lo contrario, está bajo licencia de la licencia Creative Commons Reconocimento 4.0. 10 Citogenética e evolução do cariótipo em formigas poneromorfas Cléa S.F. Mariano, Igor S. Santos, Janisete Gomes da Silva, Marco Antonio Costa, Silvia das Graças Pompolo Resumo A expansão dos estudos citogenéticos a cromossomos de todas as subfamílias e aquela partir do século XIX permitiu que informações que apresenta mais informações a respeito de ca- acerca do número e composição dos cromosso- riótipos é também a mais diversa em número de mos fossem aplicadas em estudos evolutivos, ta- espécies: Ponerinae Lepeletier de Saint Fargeau, xonômicos e na medicina humana. Em insetos, 1835. Apenas nessa subfamília observamos carió- são conhecidos os cariótipos em diversas ordens tipos com número cromossômico variando entre onde diversos padrões cariotípicos podem ser ob- 2n=8 a 120, gêneros com cariótipos estáveis, pa- servados.
    [Show full text]
  • A BRIEF HISTORY of PINE FLATWOODS in SOUTH FLORIDA Submitted by Jerry Renick, Environmental Service Manager - Wantman Group, Inc
    CouncilThe Quarterly Quarterly Newsletter of the Florida Urban Forestry Council 2016 Issue Three The Council Quarterly newsletter is published quarterly by the Florida Urban Forestry Council and is intended as an educational benefit to our members. Information may be reprinted if credit is given to the author(s) and this newsletter. All pictures, articles, advertisements, and other data are in no way to be construed as an endorsement of the author, products, services, or techniques. Likewise, the statements and opinions expressed herein are those of the individual authors and do not represent the view of the Florida Urban Forestry Council or its Executive Committee. This newsletter is made possible by the generous support of the Florida Department of Agriculture and Consumer Services, Florida Forest Service, Adam H. Putnam Commissioner. A BRIEF HISTORY OF PINE FLATWOODS IN SOUTH FLORIDA Submitted by Jerry Renick, Environmental Service Manager - Wantman Group, Inc. Pine flatwoods were first identified as pine extending into the Bahama Islands. This shrubs including saw palmetto, galberry, barrens by William Bartram in 1791 during south Florida variety of pine is also known lyonia, cocoplum, and a few other common his travels in Florida. The term flatwoods as yellow pine, swamp pine, and pitch species. They are usually inhabited with was used by the English settlers in the pine. It is estimated that pine flatwoods a diverse groundcover of grasses and early days to describe the characteristic flat as an ecosystem covered up to 50% of the wildflowers. The terrain for pine flatwoods ground with no topographic relief in south land area of Florida at one time.
    [Show full text]
  • A Revision of the Giant Amazonian Ants of the Genus Dinoponera (Hymenoptera, Formicidae)
    JHR 31:A 119–164 revision (2013) of the giant Amazonian ants of the genus Dinoponera (Hymenoptera, Formicidae) 119 doi: 10.3897/JHR.31.4335 RESEARCH ARTICLE www.pensoft.net/journals/jhr A revision of the giant Amazonian ants of the genus Dinoponera (Hymenoptera, Formicidae) Paul A. Lenhart1,†, Shawn T. Dash2,‡, William P. Mackay2,§ 1 Department of Entomology, Texas A&M University, 2475 TAMU, College Station, Texas USA 2 Department of Biological Sciences, University of Texas at El Paso, 500 West University Avenue, El Paso, Texas 79968 † urn:lsid:zoobank.org:author:6CA6E3C7-14AA-4D6B-82BF-5577F431A51A ‡ urn:lsid:zoobank.org:author:9416A527-CCE2-433E-A55F-9D51B5DCEE8A § urn:lsid:zoobank.org:author:70401E27-0F2E-46B5-BC2B-016837AF3035 Corresponding author: Paul A. Lenhart ([email protected]) Academic editor: Wojciech Pulawski | Received 16 November 2012 | Accepted 7 January2013 | Published 20 March 2013 urn:lsid:zoobank.org:pub:10404A9C-126A-44C8-BD48-5DB72CD3E3FF Citation: Lenhart PA, Dash ST, Mackay WP (2013) A revision of the giant Amazonian ants of the genus Dinoponera (Hymenoptera, Formicidae). Journal of Hymenoptera Research 31: 119–164. doi: 10.3897/JHR.31.4335 Abstract Dinoponera Roger 1861 has been revised several times. However, species limits remain questionable due to limited collection and undescribed males. We re-evaluate the species boundaries based on workers and known males. We describe the new species Dinoponera hispida from Tucuruí, Pará, Brazil and Dinoponera snellingi from Campo Grande, Mato Grosso do Sul, Brazil and describe the male of Dinoponera longipes Emery 1901. Additionally, we report numerous range extensions with updated distribution maps and provide keys in English, Spanish and Portuguese for workers and known males of Dinoponera.
    [Show full text]
  • 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.
    [Show full text]