The Effects of Wind on Foraging Srategies of Atta Cephalotes Leaf- Cutter Ants

Total Page:16

File Type:pdf, Size:1020Kb

The Effects of Wind on Foraging Srategies of Atta Cephalotes Leaf- Cutter Ants THE EFFECTS OF WIND ON FORAGING SRATEGIES OF ATTA CEPHALOTES LEAF- CUTTER ANTS By MICHAEL JOHN RODRIGUEZ B.S., Southeastern Louisiana University, 2011 A thesis submitted to the Faculty of the Graduate School of the University of Colorado in partial fulfillment of the requirement for the degree of Master of Science Department of Ecology and Evolutionary Biology 2014 This thesis entitled: The effects of wind on foraging strategies of Atta cephalotes leaf-cutter ants written by Michael John Rodriguez has been approved for the Department Ecology and Evolutionary Biology Dr. Michael Breed _____ Dr. Rebecca Safran Date The final copy of this thesis has been examined by the signatories, and we Find that both the content and the form meet acceptable presentation standards Of scholarly work in the above mentioned discipline. iii Rodriguez, Michael John (M.S., Department of Ecology and Evolutionary Biology) The effects of wind on foraging strategies of Atta cephalotes leaf-cutter ants Thesis directed by Professor Dr. Michael Breed Abstract: Successful foragers alter their behavior in response to variation in local conditions, resulting in reduction of foraging costs and maximization of resource gain. In eusocial colonies, individuals may adjust their own efforts to maximize the productivity of the colony as a whole. Maximization of colony productivity can be achieved through sub-maximal individual performance. Attine leaf-cutter ant foragers often cut leaf fragments shorter than the hind legs could allow, suggesting other factors contribute to load size determination. Several studies have shown reasons why leaf-cutter ants cut smaller loads than they could maximally carry. The effects of wind speed on leaf-cutter load size selection were examined in this study and showed conditions in which leaf-cutter foragers change their behavior to cut larger loads than normal. In response to wind treatments, foragers cut larger leaf loads and fewer minima workers hitchhiked on those leaves. This study highlights behavioral plasticity of leaf-cutter foragers in response to local conditions on the foraging trail, and it adds to our knowledge of resource allocation in central-place foraging systems. Key words: behavioral flexibility, ethology, foraging, load size selection, parasitism, social insects iv Acknowledgements Special thanks for funding from the Organization for Tropical Studies, the University of Colorado, Boulder Department of Ecology and Evolutionary Biology, Colorado Diversity Initiative, and Petridish.org contributors including: Sandra Blair, Michael Bonner, Kevin Westmoreland, Jasmine Hegman, Nicole Gorden, James Waters, Jason Steiner, Samuel J. Ciurca, Jr., James Jorasch, Gaurav Vaidya, Jaime Pawelek, Daniel Ewald, Kwame Hagan, Nicholas Barbieri, Bob Peake, Kenneth Trease, Kelly Stewart, Mustafa, Susan Fay, and Alan F. Rodriguez. Thank you to the staff and researchers of La Selva and the participants and instructors of OTS Tropical Biology course 2012-1. Thanks to my adviser, Dr. Michael Breed, and lab mates for guidance and reviews. Thank you to Dr. Catherine and Mac Macgregor. v CONTENTS Introduction...............................................................................................1 Leaf-cutter ant background.................................................................2 Foraging efficiency ......................................................................... 3-7 Hitchhiker ants ..............................................................................7 Purpose of the study ............................................................................8 Methods ............................................................................................... 9-13 Results.. ............................................................................................. 13-19 Discussion ......................................................................................... 20-24 Conclusion .................................................................................. 24-25 References ......................................................................................... 26-30 vi FIGURES Figure 1. Leaf fragment area between wind treatments ...............................................14 2. Leaf fragment area and forager head width................................................. 15 3. Forager head width between wind treatments ..............................................15 4. Interaction of forager head width and leaf fragment area between wind treatments................................................................................................16 5. Hitchhiker numbers between wind treatments ..............................................17 6. Foraging trail traffic density and leaf fragment mass ..................................18 7. Leaf fragment area between leaf type ...........................................................19 8. Forager head width between leaf type ..........................................................19 1 Introduction Successful foragers alter their behavior in response to a shifting external environment (Charnov 1976). This results in reduction of foraging costs and maximization of resource gain if local conditions vary. In eusocial colonies, individuals specializing in certain tasks may adjust their own efforts to maximize the productivity of the colony as a whole (Burd 1996a; Constant et al. 2012). Theory predicts that individuals adjust their foraging efforts to achieve optimal resource input into the nest (Charnov 1976; Wetterer 1989; Burd 1996a; Burd and Howard 2008). Interactions among nestmates and external cues allow individuals to alter their behavioral effort, especially as different biotic (parasitism, predation, nest-mate interactions) and abiotic conditions (rain, wind, temperature) vary (Hölldobler and Wilson 1990; Feener and Moss 1990; Gordon 2002; Angilletta et al. 2008; Elizalde and Folgarait 2012). Behavioral variability within a colony and behavioral flexibility displayed by individuals may contribute to the evolutionary success of colony phenotypes and to the ecological success of the eusocial Hymenoptera (Wilson 1971; Constant et al. 2012). My results from studies of foraging in a leaf-cutter ant, Atta cephalotes, add to our understanding of the complex interplay between costs and benefits in central place foraging systems and how individual behavior and recruitment behavior of leaf- cutter ants is plastic in response to abiotic and biotic external conditions, such as wind (Rudolph and Loudon1986), traffic on the foraging trail (Farji-Brener et al. 2011), or the presence of very small workers, called minima, riding on a carried load (Feener and Brown 1992; Orr et al. 1995; Porter et al. 1995). Leaf-cutting ants 2 A small percentage of ant species have polymorphic workers (Wetterer 1994), and within the fungus growing ants, family Formicidae, subfamily Myrmicinae, tribe Attini, only some species have workers with different size castes. Workers of the monomorphic Attini forage for insect carcasses, waste, and other detritus that do not require further processing. The polymorphic Attini are specialist foragers on vegetable matter (seeds, flowers, and leaves). This plant material needs special treatment to convert to a suitable substrate for fungal gardens grown by the ants and used as food. Handling of plant material in preparation for use in fungal gardening includes fragmentation, chewing, and regurgitation onto the fungal garden (Wilson 1980a, b). Leaf-cutting ants in the genera Atta and Acromyrmex have highly polymorphic workers, resulting in a high division of labor with workers specializing on tasks appropriate for their size (morphological polyethism) (Wilson 1980a, b). In Atta cephalotes leaf-cutter ants, the species addressed in this study, the largest workers can be 200 times the size of the smallest workers (Weber 1972). The large, major, workers and intermediate, media, workers act as soldiers and foragers, made effective by their large bodies and mandibular muscles. The smaller, or minima, workers take care of the brood and garden and maintain the trails (Hughes and Goulson 2001). Inside the nest, minima gardeners fragment the forage into a pulp that they feed to basiodiomycetes fungi which are cultured as the primary food source for their developing larvae. To a lesser extent adults also feed on the fungi (Weber 1972; Quinlan & Cherrett 1979; Benckiser 2011). The fungal gardens are analogous to human agriculture (Benckiser 2011). Minima workers are primarily fungal caretakers but have a secondary role as defenders of adult ants against parasitic phorid flies (Phoridae: Pseudoacteon sp.). Minima workers hitchhike rides aboard leaf fragments carried back by larger workers (Wilson 1980a, b; Feener and Moss 3 1990; Vieira-Neto et al. 2006) and fend off these flies. Foragers can travel for hours over long distances on dedicated and manicured trails, recorded to span 300 m from the nest entrance, with a mean distance of 50 m (Lewis et al. 1974; Wetterer 1990). Foragers travelling back to the nest carrying loads are more vulnerable to parasitoid attack than unladen workers, and hitchhiking ants offer defense, rearing up on hind legs to grab the fly or to block oviposition (Feener and Moss 1990; Vieira-Neto et al. 2006). Considering the long travel times of foragers and their vulnerability while carrying loads, hitchhikers offer a valuable defense from parasitoid enemies. In addition to defense, hitchhikers sometimes work to remove trichomes on
Recommended publications
  • The Mesosomal Anatomy of Myrmecia Nigrocincta Workers and Evolutionary Transformations in Formicidae (Hymeno- Ptera)
    7719 (1): – 1 2019 © Senckenberg Gesellschaft für Naturforschung, 2019. The mesosomal anatomy of Myrmecia nigrocincta workers and evolutionary transformations in Formicidae (Hymeno- ptera) Si-Pei Liu, Adrian Richter, Alexander Stoessel & Rolf Georg Beutel* Institut für Zoologie und Evolutionsforschung, Friedrich-Schiller-Universität Jena, 07743 Jena, Germany; Si-Pei Liu [[email protected]]; Adrian Richter [[email protected]]; Alexander Stößel [[email protected]]; Rolf Georg Beutel [[email protected]] — * Corresponding author Accepted on December 07, 2018. Published online at www.senckenberg.de/arthropod-systematics on May 17, 2019. Published in print on June 03, 2019. Editors in charge: Andy Sombke & Klaus-Dieter Klass. Abstract. The mesosomal skeletomuscular system of workers of Myrmecia nigrocincta was examined. A broad spectrum of methods was used, including micro-computed tomography combined with computer-based 3D reconstruction. An optimized combination of advanced techniques not only accelerates the acquisition of high quality anatomical data, but also facilitates a very detailed documentation and vi- sualization. This includes fne surface details, complex confgurations of sclerites, and also internal soft parts, for instance muscles with their precise insertion sites. Myrmeciinae have arguably retained a number of plesiomorphic mesosomal features, even though recent mo- lecular phylogenies do not place them close to the root of ants. Our mapping analyses based on previous morphological studies and recent phylogenies revealed few mesosomal apomorphies linking formicid subgroups. Only fve apomorphies were retrieved for the family, and interestingly three of them are missing in Myrmeciinae. Nevertheless, it is apparent that profound mesosomal transformations took place in the early evolution of ants, especially in the fightless workers.
    [Show full text]
  • Supporting Information
    Supporting Information Renewed diversification is associated with new ecological opportunity in the Neotropical turtle ants Shauna L. Price, Scott Powell, Daniel J. C. Kronauer, Lucy A. P. Tran, Naomi E. Pierce, and R. K. Wayne Appendix S1: Materials and methods Molecular methods Molecular work was conducted at UCLA and Harvard. At UCLA PCR was performed in 25 µL volumes: 16.3 µL ddH2O, 2.5 µL 10x PCR Buffer, 1.5 µL 25 mM MgCl2, 0.5 µL dNTPs (25mM each), 1 µL DMSO, 0.2 µL of each primer (25x), 0.2 µL QIAGEN Taq DNA Polymerase, and 2 µL DNA. PCR cycles were: initial denaturation for 3 min at 94o, followed by 30 cycles of 94o for 30 s, 50-58o for 30 s, and 72o for 45 s, and a final extension of 72o for 5 min. Annealing temperatures depended on the gene segment amplified. PCR products were purified with Exonuclease I and Shrimp Alkaline Phosphatase. At Harvard PCR was performed in 25 µL volumes with the same PCR conditions as UCLA and a cocktail containing 15.05 µL ddH2O, 2.5 µL 10x PCR Buffer, 1 µL 25 mM MgCl2, 0.25 µL dNTPs (25mM each), 2 µL of each primer (10x), 0.2 µL QIAGEN Taq DNA Polymerase, and 2 µL DNA. PCR products were sent to Macrogen for purification. All loci were sequenced in both directions using an ABI 3730 automated sequencer with Big Dye Terminator chemistry (Applied Biosystems Inc) either at Macrogen or the Cornell University Life Sciences Core Laboratories Center. Heterozygous positions were left ambiguous and occurred in less than 0.0007% of nuclear base pairs.
    [Show full text]
  • Size-Related Foraging Behaviour of the Leaf-Cutting Ant Atta Colornbica
    Size-related foraging behaviour of the leaf-cutting ant Atta colornbica DAVESHUTLER' Department of Biology, Carleton University, Ottawa, Ont., Canada KlS 5B6 AND ADELE MULLIE Department of Biology, Queen's University, Kingston, Ont., Canada K7L IB6 September 12, 1990 SHUTLER,D., and MULLIE,A. 1991. Size-related foraging behaviour of the leaf-cutting ant Atta colombica. Can. J. Zool. 69: 1530- 1533 In a Costa Rican forest adjacent to cattle pasture, larger individuals of the leaf-cutting ant Atta colombica carried heavier loads and foraged farther from the colony, as predicted by foraging theory. Counter to foraging theory, individual ants did not increase their load mass if they foraged farther from the colony. However, the colony avoided this apparent inefficiency by sending larger ants to more distant trees. The colony harvested simultaneously from several individuals of the same tree species, even though distant trees were twice as far from the colony as nearby trees. The reasons for this behaviour require further investigation. In a wide foraging trail, larger ants travelled faster than their smaller counterparts. In addition, ant velocity was reduced when loads were experimentally supplemented, and increased when loads were experimentally reduced. Ants using narrow trails in the leaf litter may all be constrained to travel at the same speed, irrespective of load or body size, simply because they get in each other's way. SHUTLER,D., et MULLIE,A. 1991. Size-related foraging behaviour of the leaf-cutting ant Atta colombica. Can. J. Zool. 69 : 1530- 1533 Dans une foret du Costa Rica adjacente B un piturage, ce sont les individus les plus gros de la fourmi dkcoupeuse Atta colombica qui transportent les fardeaux les plus lourds et qui s'kloignent le plus de la colonie pour chercher leur nourriture; c'est d'ailleurs ce que laksait prkvoir la thkorie de la quete optimale.
    [Show full text]
  • Hymenoptera: Formicidae) in Brazilian Forest Plantations
    Forests 2014, 5, 439-454; doi:10.3390/f5030439 OPEN ACCESS forests ISSN 1999-4907 www.mdpi.com/journal/forests Review An Overview of Integrated Management of Leaf-Cutting Ants (Hymenoptera: Formicidae) in Brazilian Forest Plantations Ronald Zanetti 1, José Cola Zanuncio 2,*, Juliana Cristina Santos 1, Willian Lucas Paiva da Silva 1, Genésio Tamara Ribeiro 3 and Pedro Guilherme Lemes 2 1 Laboratório de Entomologia Florestal, Universidade Federal de Lavras, 37200-000, Lavras, Minas Gerais, Brazil; E-Mails: [email protected] (R.Z.); [email protected] (J.C.S.); [email protected] (W.L.P.S.) 2 Departamento de Entomologia, Universidade Federal de Viçosa, 36570-900, Viçosa, Minas Gerais, Brazil; E-Mail: [email protected] 3 Departamento de Ciências Florestais, Universidade Federal de Sergipe, 49100-000, São Cristóvão, Sergipe State, Brazil; E-Mail: [email protected] * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +55-31-389-925-34; Fax: +55-31-389-929-24. Received: 18 December 2013; in revised form: 19 February 2014 / Accepted: 19 February 2014 / Published: 20 March 2014 Abstract: Brazilian forest producers have developed integrated management programs to increase the effectiveness of the control of leaf-cutting ants of the genera Atta and Acromyrmex. These measures reduced the costs and quantity of insecticides used in the plantations. Such integrated management programs are based on monitoring the ant nests, as well as the need and timing of the control methods. Chemical control employing baits is the most commonly used method, however, biological, mechanical and cultural control methods, besides plant resistance, can reduce the quantity of chemicals applied in the plantations.
    [Show full text]
  • Leaf-Cutting Ant Herbivory in Successional and Agricultural Tropical Ecosystems Author(S): Chantal M
    Leaf-Cutting Ant Herbivory in Successional and Agricultural Tropical Ecosystems Author(s): Chantal M. Blanton and John J. Ewel Reviewed work(s): Source: Ecology, Vol. 66, No. 3 (Jun., 1985), pp. 861-869 Published by: Ecological Society of America Stable URL: http://www.jstor.org/stable/1940548 . Accessed: 01/11/2012 15:22 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp . JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. Ecological Society of America is collaborating with JSTOR to digitize, preserve and extend access to Ecology. http://www.jstor.org Ecology,66(3), 1985, pp. 861-869 ? 1985by the Ecological Society of America LEAF-CUTTING ANT HERBIVORY IN SUCCESSIONAL AND AGRICULTURAL TROPICAL ECOSYSTEMS1 Chantal M. Blanton and John J. Ewel Departmentof Botany, Universityof Florida, Gainesville,Florida 32611 USA Abstract. Herbivory by Atta cephalotes was measured in four plant communities of different complexityin Costa Rica. The fourcommunities were a monocultureof cassava {Manihot esculenta) and three diverse assemblages, each 1.5 yr old: (1) successional vegetation,unmodified by the in- vestigators;(2) imitationof succession, a communityof investigator-introducedspecies designed to mimic the unmodified succession; and (3) enriched succession, a successional vegetation that the investigatorshad augmentedby propagule inputs. Each ant colony had access to all fourcommunity typessimultaneously.
    [Show full text]
  • Prevalence and Impact of a Virulent Parasite on a Tripartite Mutualism
    Oecologia (2001) 128:99–106 DOI 10.1007/s004420100630 Cameron R. Currie Prevalence and impact of a virulent parasite on a tripartite mutualism Received: 20 July 2000 / Accepted: 14 December 2000 / Published online: 28 February 2001 © Springer-Verlag 2001 Abstract The prevalence and impact of a specialized other interspecific interactions, such as competition and microfungal parasite (Escovopsis) that infects the fungus predation (Freeland 1983; Price et al. 1986; Schall 1992; gardens of leaf-cutting ants was examined in the labora- Hudson and Greenman 1998; Yan et al. 1998). Within tory and in the field in Panama. Escovopsis is a common mutualistic associations, most of the research on para- parasite of leaf-cutting ant colonies and is apparently sites has focused on ‘cheaters’: taxa that are closely re- more frequent in Acromyrmex spp. gardens than in gar- lated to one of the mutualists but do not co-operate, ob- dens of the more phylogenetically derived genus Atta taining a reward without providing a benefit in return spp. In addition, larger colonies of Atta spp. appear to be (Boucher et al. 1982; Mainero and Martinez del Rio less frequently infected with the parasite. In this study, 1985). The interest in ‘cheaters’ within mutualisms is at the parasite Escovopsis had a major impact on the suc- least partially based on the long-term stability of co- cess of this mutualism among ants, fungi, and bacteria. operation being a challenge to evolutionary theory (e.g., Infected colonies had a significantly lower rate of fungus Addicott 1996; Morris 1996; Pellmyr et al. 1996; Bao garden accumulation and produced substantially fewer and Addicott 1998).
    [Show full text]
  • Ant–Fungus Species Combinations Engineer Physiological Activity Of
    © 2014. Published by The Company of Biologists Ltd | The Journal of Experimental Biology (2014) 217, 2540-2547 doi:10.1242/jeb.098483 RESEARCH ARTICLE Ant–fungus species combinations engineer physiological activity of fungus gardens J. N. Seal1,2,*, M. Schiøtt3 and U. G. Mueller2 ABSTRACT such complexity, the fungus-gardening insects have evolved obligate Fungus-gardening insects are among the most complex organisms macro-symbioses with specific clades of fungi, and use fungal because of their extensive co-evolutionary histories with obligate symbionts essentially as an external digestive organ that allows the fungal symbionts and other microbes. Some fungus-gardening insect insect to thrive on otherwise non-digestible substrates, such as lineages share fungal symbionts with other members of their lineage structural carbohydrates of plants (e.g. cellulose) (Aanen et al., and thus exhibit diffuse co-evolutionary relationships, while others 2002; Aylward et al., 2012a; Aylward et al., 2012b; Bacci et al., exhibit little or no symbiont sharing, resulting in host–fungus fidelity. 1995; Farrell et al., 2001; De Fine Licht and Biedermann, 2012; The mechanisms that maintain this symbiont fidelity are currently Martin, 1987a; Mueller et al., 2005). One of the most striking unknown. Prior work suggested that derived leaf-cutting ants in the attributes of these symbioses is the degree of physiological genus Atta interact synergistically with leaf-cutter fungi (Attamyces) integration: the insect host functions as a distributor of fungal by exhibiting higher fungal growth rates and enzymatic activities than enzymes, which digest plant fibers external to the insect’s body when growing a fungus from the sister-clade to Attamyces (so-called (Aanen and Eggleton, 2005; Aylward et al., 2012b; De Fine Licht ‘Trachymyces’), grown primarily by the non-leaf cutting and Biedermann, 2012; De Fine Licht et al., 2013; Martin, 1987b; Trachymyrmex ants that form, correspondingly, the sister-clade to Schiøtt et al., 2010).
    [Show full text]
  • The Impact of the Leaf Cutter Ant Atta Colombica on the Energy Flow of a Tropical West Forest Author(S): Ariel E
    The Impact of the Leaf Cutter Ant Atta Colombica on the Energy Flow of a Tropical West Forest Author(s): Ariel E. Lugo, Edward G. Farnworth, Douglas Pool, Patricio Jerez, Glen Kaufman Source: Ecology, Vol. 54, No. 6 (Nov., 1973), pp. 1292-1301 Published by: Ecological Society of America Stable URL: http://www.jstor.org/stable/1934191 Accessed: 21/07/2010 10:41 Your use of the JSTOR archive indicates your acceptance of JSTOR's Terms and Conditions of Use, available at http://www.jstor.org/page/info/about/policies/terms.jsp. JSTOR's Terms and Conditions of Use provides, in part, that unless you have obtained prior permission, you may not download an entire issue of a journal or multiple copies of articles, and you may use content in the JSTOR archive only for your personal, non-commercial use. Please contact the publisher regarding any further use of this work. Publisher contact information may be obtained at http://www.jstor.org/action/showPublisher?publisherCode=esa. Each copy of any part of a JSTOR transmission must contain the same copyright notice that appears on the screen or printed page of such transmission. JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. Ecological Society of America is collaborating with JSTOR to digitize, preserve and extend access to Ecology.
    [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]
  • Download Download
    Behavioral Ecology Symposium ’96: Cushing 165 MYRMECOMORPHY AND MYRMECOPHILY IN SPIDERS: A REVIEW PAULA E. CUSHING The College of Wooster Biology Department 931 College Street Wooster, Ohio 44691 ABSTRACT Myrmecomorphs are arthropods that have evolved a morphological resemblance to ants. Myrmecophiles are arthropods that live in or near ant nests and are considered true symbionts. The literature and natural history information about spider myrme- comorphs and myrmecophiles are reviewed. Myrmecomorphy in spiders is generally considered a type of Batesian mimicry in which spiders are gaining protection from predators through their resemblance to aggressive or unpalatable ants. Selection pressure from spider predators and eggsac parasites may trigger greater integration into ant colonies among myrmecophilic spiders. Key Words: Araneae, symbiont, ant-mimicry, ant-associates RESUMEN Los mirmecomorfos son artrópodos que han evolucionado desarrollando una seme- janza morfológica a las hormigas. Los Myrmecófilos son artrópodos que viven dentro o cerca de nidos de hormigas y se consideran verdaderos simbiontes. Ha sido evaluado la literatura e información de historia natural acerca de las arañas mirmecomorfas y mirmecófilas . El myrmecomorfismo en las arañas es generalmente considerado un tipo de mimetismo Batesiano en el cual las arañas están protegiéndose de sus depre- dadores a través de su semejanza con hormigas agresivas o no apetecibles. La presión de selección de los depredadores de arañas y de parásitos de su saco ovopositor pueden inducir una mayor integración de las arañas mirmecófílas hacia las colonias de hor- migas. Myrmecomorphs and myrmecophiles are arthropods that have evolved some level of association with ants. Myrmecomorphs were originally referred to as myrmecoids by Donisthorpe (1927) and are defined as arthropods that mimic ants morphologically and/or behaviorally.
    [Show full text]
  • Hymenoptera: Formicidae) Audrey Marie Hernando University of Texas at El Paso, [email protected]
    University of Texas at El Paso DigitalCommons@UTEP Open Access Theses & Dissertations 2012-01-01 The mpI act of Solar Radiation on the Distribution of The Red Imported Fire Ant, Solenopsis invicta (Hymenoptera: Formicidae) Audrey Marie Hernando University of Texas at El Paso, [email protected] Follow this and additional works at: https://digitalcommons.utep.edu/open_etd Part of the Biology Commons, and the Environmental Sciences Commons Recommended Citation Hernando, Audrey Marie, "The mpI act of Solar Radiation on the Distribution of The Red Imported Fire Ant, Solenopsis invicta (Hymenoptera: Formicidae)" (2012). Open Access Theses & Dissertations. 2105. https://digitalcommons.utep.edu/open_etd/2105 This is brought to you for free and open access by DigitalCommons@UTEP. It has been accepted for inclusion in Open Access Theses & Dissertations by an authorized administrator of DigitalCommons@UTEP. For more information, please contact [email protected]. THE IMPACT OF SOLAR RADIATION ON THE DISTRIBUTION OF THE RED IMPORTED FIRE ANT, Solenopsis invicta (HYMENOPTERA: FORMICIDAE) AUDREY MARIE HERNANDO, M.S. Environmental Science & Engineering Program APPROVED: William P. Mackay, Ph.D., Chair Raed Aldouri, Ph.D. Jorge Gardea-Torresdey, Ph.D. Jerry Johnson, Ph.D. John Walton, Ph.D. Benjamin C. Flores, Ph.D Dean of the Graduate School. Copyright © by Audrey Marie Hernando 2012 Dedication My dissertation would not have been possible without the help and support of my family, committee, and friends. My family: my father, my sons and their families have believed in me and encouraged me. Without their tireless support, and patience, I would not have been able to complete this work.
    [Show full text]
  • Programacao Formigas.Pdf
    LOCALIZAÇÃO DOS SALÕES / MEETING ROOMS MAP BEM VINDOS EM FORTALEZA BEM VINDOS EM FORTALEZA BEM-VINDOS A FORTALEZA WELCOME TO FORTALEZA DOMINGO, 01 / SUNDAY, 01 16:00 – 19:00: Entrega de material / Registration 19:00 – 20:30: Cerimônia de abertura / Opening ceremony 20:30 – 22:30: Cocktail SEGUNDA-FEIRA, 02/ MONDAY, 02 8:00 – 9:00: Entrega de material / Registration 9:00 – 10:00: Conferência / Plenary talk (Salão Safira & Topázio) “Colony foundation strategies in ants: alone or in a group?”. Christian Peeters (Université Pierre et Marie Curie – France) 10:00 – 10:30: Coffee break 10:30 - 12:00 Mesa-redonda / Round table (Salão Safira & Topázio) “Exploring the frontiers of knowledge in ant evolution”. Convidados / Invited speakers: Márcio Roberto Pie (UFPR - Brazil), Corrie Moreau (Field Museum of Natural History - Chicago - USA), Seán G. Brady (Smithsonian Institute - USA) (canceled), Maurício Bacci Jr. (UNESP - Brazil) Mesa-redonda / Round table (Salão Ametista) “Mechanisms of community assembly in ants: contrasting evidence from different ecological contexts”. Convidados / Invited speakers: Scott Powell (The George Washington University - USA), Flávio de Carvalho Camarota (UFU - Brazil), Nathan J. Sanders (University of Tennessee - USA), Elizabeth Pringle (University of Michigan - USA) 12:00 – 13:30: Almoço / Lunch time 13:30 – 14:30: Conferência / Plenary talk (Salão Safira & Topázio) “The phylogeny and evolution of ants”. Philip S. Ward (University of California at Davis – USA) 14:30 – 15:30: Sessões de apresentações orais / Oral presentation
    [Show full text]