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A Small Number of Workers with Specific Personality Traits Perform Tool Use in Ants Istva´ N Maa´ K1,2, Garyk Roelandt3, Patrizia D’Ettorre3,4*
RESEARCH ARTICLE A small number of workers with specific personality traits perform tool use in ants Istva´ n Maa´ k1,2, Garyk Roelandt3, Patrizia d’Ettorre3,4* 1Department of Ecology, University of Szeged, Szeged, Hungary; 2Museum and Institute of Zoology, Polish Academy of Science, Warsaw, Poland; 3Laboratory of Experimental and Comparative Ethology UR 4443, University Sorbonne Paris Nord, Villetaneuse, France; 4Institut Universitaire de France (IUF), Paris, France Abstract Ants use debris as tools to collect and transport liquid food to the nest. Previous studies showed that this behaviour is flexible whereby ants learn to use artificial material that is novel to them and select tools with optimal soaking properties. However, the process of tool use has not been studied at the individual level. We investigated whether workers specialise in tool use and whether there is a link between individual personality traits and tool use in the ant Aphaenogaster senilis. Only a small number of workers performed tool use and they did it repeatedly, although they also collected solid food. Personality predicted the probability to perform tool use: ants that showed higher exploratory activity and were more attracted to a prey in the personality tests became the new tool users when previous tool users were removed from the group. This suggests that, instead of extreme task specialisation, variation in personality traits within the colony may improve division of labour. Introduction Tool use is a widespread phenomenon within the animal kingdom (Shumaker et al., 2011; Sanz et al., 2013) and new examples of animal tool use are regularly discovered, such as recently in *For correspondence: [email protected] pigs (Root-Bernstein et al., 2019) and seabirds (Fayet et al., 2020). -
Complexity and Behaviour in Leptothorax Ants
Complexity and behaviour in Leptothorax ants Octavio Miramontes Universidad Nacional Aut´onomade M´exico ISBN 978-0-9831172-2-3 Mexico City Boston Vi¸cosa Madrid Cuernavaca Beijing CopIt ArXives 2007 Washington, DC CopIt ArXives Mexico City Boston Vi¸cosa Madrid Cuernavaca Beijing Copyright 1993 by Octavio Miramontes Published 2007 by CopIt ArXives Washington, DC All property rights of this publications belong to the author who, however, grants his authorization to the reader to copy, print and distribute his work freely, in part or in full, with the sole conditions that (i) the author name and original title be cited at all times, (ii) the text is not modified or mixed and (iii) the final use of the contents of this publication must be non commercial Failure to meet these conditions will be a violation of the law. Electronically produced using Free Software and in accomplishment with an Open Access spirit for academic publications Social behaviour in ants of the genus Leptothorax is reviewed. Attention is paid to the existence of collective robust periodic oscillations in the activity of ants inside the nest. It is known that those oscillations are the outcome of the process of short-distance interactions among ants and that the activity of individual workers is not periodic. Isolated workers can activate spontaneously in a unpredictable fashion. A model of an artificial society of computer automata endowed with the basic behavioural traits of Leptothorax ants is presented and it is demonstrated that collective periodic oscillations in the activity domain can exist as a consequence of interactions among the automata. -
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Myrmecological News 23 41-59 Vienna, September 2016 Analyzing large-scale and intranidal phenotype distributions in eusocial Hymenoptera – a taxonomic tool to distinguish intraspecific dimorphism from heterospecificity Bernhard SEIFERT Abstract Ant and termite nests are long-term stable, semi-closed systems constantly producing conspecific worker populations of related individuals over many generations. Accordingly, nests of these eusocial insects, as they are found in nature, offer free of cost an analysis situation that has to be generated in other groups of organisms by controlled rearing experiments. A test system based on analyzing intranidal and large-scale phenotype distributions and comparing the observed distributions with predictions for different scenarios of heterospecificity and intraspecific dimorphism is introduced by a case study on ants. The test system, named DIMORPH test, allows a taxonomist to distinguish if discrete character syndromes represent separate species or an intraspecific phenomenon. One of the most important parameters within the test system is the abundance and distribution of phenotypically mixed nest populations. Five biological explanations are possible for ant nests with a mixture of discrete phenotypes: They may represent (1) geneti- cally determined intraspecific morphs, (2) intraspecific modifications induced by environmental factors, (3) the associ- ation of a temporary social parasite with a host species, (4) the association of a permanent social parasite with a host species, and (5) a parabiotic association of two basically independent (self-sustaining) species. The paper explains the biological background of the scenarios (1) to (5) and presents mathematical models and generalizations from empirical data to predict phenotype distributions for each scenario under variable conditions. -
Space, Habitat and Isolation Are the Key Determinants of Tree Colonization by the Carpenter Ant in Plantation Forests
Article Space, Habitat and Isolation are the Key Determinants of Tree Colonization by the Carpenter Ant in Plantation Forests Adam Véle 1,2 and Jakub Horák 1,3,* 1 Department of Forest Protection and Entomology, Faculty of Forestry and Wood Sciences, Czech University of Life Sciences Prague, Kamýcká 1176, CZ-165 21 Prague, Czech Republic 2 Forestry & Game Management Research Institute, Strnady 136, CZ-252 02 Jílovištˇe,Czech Republic 3 Department of Biology, Faculty of Science, University of Hradec Králové, Rokitanského 62, CZ-500 03 Hradec Králové, Czech Republic * Correspondence: [email protected] Received: 27 June 2019; Accepted: 25 July 2019; Published: 27 July 2019 Abstract: Forest plantations are still often considered the antithesis of real nature. However, plantations can host many organisms. The problem is that some of the hosted species are regarded ad hoc as pests. The main aim of our paper was to study the carpenter ant (Camponotus ligniperdus) in windstorm habitats. We studied forests in East Bohemia, Czech Republic, and focused on the spatial distribution of snapped trees and the influence of selected forest characteristics on the incidence of ant nests. We found that the nests in the study area mainly occurred in Norway spruce, which is the most commercially important tree in the majority of Central Europe. More than one quarter of the snapped trees were inhabited by the ants. We found that nests exhibited a spatially autocorrelated pattern that differed on spatial scales. The most important characteristic of the host tree for determining carpenter ant nests was the presence of brown rot, and the majority of tree nests were isolated from forest openings. -
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Myrmecological News 16 7-23 Vienna, January 2012 The ants (Hymenoptera: Formicidae) are unique and enigmatic hosts of prevalent Wolbachia (Alphaproteobacteria) symbionts Jacob A. RUSSELL Abstract Intracellular bacteria from the genus Wolbachia are the most prevalent microbes found among the arthropods, shaping the ecology and evolution of their hosts through selfish and mutualistic means. The ants comprise an interesting group of Wolbachia hosts given their status as eusocial haplodiploids with commonly biased sex ratios. Although experimental hurdles have obscured Wolbachia's impacts on the ants, published findings have still managed to document unique aspects of ant-Wolbachia interactions, including exceptional levels of multiple infection, symbiont curing, and potential effects of host mobility on the spread and evolution of these heritable symbionts. To further develop hypotheses on the significance of Wolbachia and the forces that shape their distributions across the ants and beyond, I synthesize the results of a growing body of literature that has largely focused on symbiont prevalence. Results from surveys across ~ 455 species indicate that ants are common hosts, although infection levels differ among ant genera and likely across taxa with different modes of colony founding. A meta-analysis of Wolbachia distributions across ~ 2,600 other arthropod species revealed a similar pattern of variation among lower-level taxa, suggesting that the ecological and evolutionary shifts governing infection dynamics have occurred on recent timescales. Phylogenetic analyses suggest that ant-associated Wolbachia symbionts show some degree of host specificity. However, related strains are generally distributed across ants from multiple tribes and genera, while ants from different locations harbor strains from distinct lineages on the Wolbachia phylogeny. -
No Impact on Queen Turnover, Inbreeding, and Population Genetic Differentiation in the Ant Formica Selysi
Evolution, 58(5), 2004, pp. 1064±1072 VARIABLE QUEEN NUMBER IN ANT COLONIES: NO IMPACT ON QUEEN TURNOVER, INBREEDING, AND POPULATION GENETIC DIFFERENTIATION IN THE ANT FORMICA SELYSI MICHEL CHAPUISAT,1 SAMUEL BOCHERENS, AND HERVEÂ ROSSET Department of Ecology and Evolution, Biology Building, University of Lausanne, 1015 Lausanne, Switzerland 1E-mail: [email protected] Abstract. Variation in queen number alters the genetic structure of social insect colonies, which in turn affects patterns of kin-selected con¯ict and cooperation. Theory suggests that shifts from single- to multiple-queen colonies are often associated with other changes in the breeding system, such as higher queen turnover, more local mating, and restricted dispersal. These changes may restrict gene ¯ow between the two types of colonies and it has been suggested that this might ultimately lead to sympatric speciation. We performed a detailed microsatellite analysis of a large population of the ant Formica selysi, which revealed extensive variation in social structure, with 71 colonies headed by a single queen and 41 by multiple queens. This polymorphism in social structure appeared stable over time, since little change in the number of queens per colony was detected over a ®ve-year period. Apart from queen number, single- and multiple-queen colonies had very similar breeding systems. Queen turnover was absent or very low in both types of colonies. Single- and multiple-queen colonies exhibited very small but signi®cant levels of inbreeding, which indicates a slight deviation from random mating at a local scale and suggests that a small proportion of queens mate with related males. -
Hymenoptera: Formicidae)
THE ORIGIN OF WORKERLESS PARASITES IN LEPTOTHORAX (S.STR.) (HYMENOPTERA: FORMICIDAE) BY JORGEN HEINZE Theodor-Boveri-Institut (Biozentrum der Universitit), LS Verhaltensphysiologie und Soziobiologie, Am Hubland, D-97074 Wtirzburg, F.R.G. ABSTRACT The evolutionary origin of workerless parasitic ants parasitizing colonies of Leptothorax (s.str.) is investigated using data on mor- phology, chromosome number, and allozyme phenotype of both social parasites and their hosts. Of the three previously proposed pathways, the evolution of workerless parasites from guest ants or slave-makers is unlikely, at least according to a phenogram obtained by UPGMA clustering of Nei's similarities based on seven enzymes. Intraspecific evolution of the workerless parasites Doronomyrmex goesswaldi, D. kutteri, and D. pacis from their common host, Leptothorax acervorum cannot be excluded with the present data. The workerless parasite L. paraxenus, however, clearly differs from its host, L. cf. canadensis, in morphology and biochemistry, and most probably did not evolve from the latter species. It is proposed to synonymize Doronomyrmex under Lep- tothorax (s.str.). INTRODUCTION Eusocial insects by definition are characterized by a division of labor between non-reproductive workers and reproductive queens. Nevertheless, in a small minority of ant, bee, and wasp species, the worker caste has been secondarily lost. Instead of founding their own colonies solitarily, the queens of these workerless social para- sites invade the nests of other, often closely related host species and exploit the present worker force to rear their own young. In 1present address: Zool. Inst. I, Univ. Erlangen-Ntirnberg, Staudtstrasse 5, D-91058 Erlangen, Germany Manuscript received 19 January 1996. -
Encyclopedia of Social Insects
G Guests of Social Insects resources and homeostatic conditions. At the same time, successful adaptation to the inner envi- Thomas Parmentier ronment shields them from many predators that Terrestrial Ecology Unit (TEREC), Department of cannot penetrate this hostile space. Social insect Biology, Ghent University, Ghent, Belgium associates are generally known as their guests Laboratory of Socioecology and Socioevolution, or inquilines (Lat. inquilinus: tenant, lodger). KU Leuven, Leuven, Belgium Most such guests live permanently in the host’s Research Unit of Environmental and nest, while some also spend a part of their life Evolutionary Biology, Namur Institute of cycle outside of it. Guests are typically arthropods Complex Systems, and Institute of Life, Earth, associated with one of the four groups of eusocial and the Environment, University of Namur, insects. They are referred to as myrmecophiles Namur, Belgium or ant guests, termitophiles, melittophiles or bee guests, and sphecophiles or wasp guests. The term “myrmecophile” can also be used in a broad sense Synonyms to characterize any organism that depends on ants, including some bacteria, fungi, plants, aphids, Inquilines; Myrmecophiles; Nest parasites; and even birds. It is used here in the narrow Symbionts; Termitophiles sense of arthropods that associated closely with ant nests. Social insect nests may also be parasit- Social insect nests provide a rich microhabitat, ized by other social insects, commonly known as often lavishly endowed with long-lasting social parasites. Although some strategies (mainly resources, such as brood, retrieved or cultivated chemical deception) are similar, the guests of food, and nutrient-rich refuse. Moreover, nest social insects and social parasites greatly differ temperature and humidity are often strictly regu- in terms of their biology, host interaction, host lated. -
Irish Ants (Hymenoptera, Formicidae): Distribution, Conservation and Functional Relationships
Irish Ants (Hymenoptera, Formicidae): Distribution, Conservation and Functional Relationships Submitted by: Dipl. Biol. Robin Niechoj Supervisor: Prof. John Breen Submitted in accordance with the academic requirements for the Degree of Doctor of Philosophy to the Department of Life Sciences, Faculty of Science and Engineering, University of Limerick Limerick, April 2011 Declaration I hereby declare that I am the sole author of this thesis and that it has not been submitted for any other academic award. References and acknowledgements have been made, where necessary, to the work of others. Signature: Date: Robin Niechoj Department of Life Sciences Faculty of Science and Engineering University of Limerick ii Acknowledgements/Danksagung I wish to thank: Dr. John Breen for his supervision, encouragement and patience throughout the past 5 years. His infectious positive attitude towards both work and life was and always will be appreciated. Dr. Kenneth Byrne and Dr. Mogens Nielsen for accepting to examine this thesis, all the CréBeo team for advice, corrections of the report and Dr. Olaf Schmidt (also) for verification of the earthworm identification, Dr. Siobhán Jordan and her team for elemental analyses, Maria Long and Emma Glanville (NPWS) for advice, Catherine Elder for all her support, including fieldwork and proof reading, Dr. Patricia O’Flaherty and John O’Donovan for help with the proof reading, Robert Hutchinson for his help with the freeze-drying, and last but not least all the staff and postgraduate students of the Department of Life Sciences for their contribution to my work. Ich möchte mich bedanken bei: Katrin Wagner für ihre Hilfe im Labor, sowie ihre Worte der Motivation. -
Redalyc.Polinización Por Hormigas
Ecosistemas ISSN: 1132-6344 [email protected] Asociación Española de Ecología Terrestre España de Vega, C.; Gómez, J.M. Polinización por hormigas: conceptos, evidencias y futuras direcciones Ecosistemas, vol. 23, núm. 3, septiembre-diciembre, 2014, pp. 48-57 Asociación Española de Ecología Terrestre Alicante, España Disponible en: http://www.redalyc.org/articulo.oa?id=54032954007 Cómo citar el artículo Número completo Sistema de Información Científica Más información del artículo Red de Revistas Científicas de América Latina, el Caribe, España y Portugal Página de la revista en redalyc.org Proyecto académico sin fines de lucro, desarrollado bajo la iniciativa de acceso abierto Ecosistemas 23(3): 48-57 [Septiembre-Diciembre 2014] Doi.: 10.7818/ECOS.2014.23-3.07 Artículo publicado en Open Access bajo los términos AEET de Creative Commons attribution Non Comercial License 3.0. eREVIScTA CoIENTÍFsICA DiEs ECOLtOGeÍA Y MmEDIO AaMBIENs TE ASOCIACIÓN ESPAÑOLA MONOGRÁFICO: ISSN 1697-2473 / Open access DE ECOLOGÍA TERRESTRE Ecología reproductiva de las plantas disponible en www.revistaecosistemas.net Polinización por hormigas: conceptos, evidencias y futuras direcciones C. de Vega 1*, J.M. Gómez 2,3 (1) Estación Biológica de Doñana, Consejo Superior de Investigaciones Científicas (CSIC), Avenida de Américo Vespucio s/n, 41092 Sevilla, España. (2) Estación Experimental de Zonas Áridas. CSIC. Ctra. Sacramento s/n. La Cañada de San Urbano. 04120 Almería, España. (3) Departamento de Ecología. Facultad de Ciencias. Universidad de Granada. 18071 Granada, España. * Autor de correspondencia: C. de Vega [[email protected]] > Recibido el 31 de diciembre de 2013 - Aceptado el 10 de marzo de 2014 de Vega, C., Gómez, J.M. -
Rossomyrmex, the Slave-Maker Ants from the Arid Steppe Environments
Hindawi Publishing Corporation Psyche Volume 2013, Article ID 541804, 7 pages http://dx.doi.org/10.1155/2013/541804 Review Article Rossomyrmex, the Slave-Maker Ants from the Arid Steppe Environments F. Ruano,1 O. Sanllorente,1,2 A. Lenoir,3 and A. Tinaut1 1 Departamento de Zoolog´ıa, Universidad de Granada, 18071 Granada, Spain 2 Departamento de Biolog´ıa Experimental, Facultad de Ciencias Experimentales, Universidad de Jaen,´ Campus Las Lagunillas s/n, 23071 Jaen,´ Spain 3 Institut de Recherche sur la Biologie de l’Insecte, IRBI-UMR CNRS 7261, Faculte´ des Sciences et Techniques, UniversiteFranc´ ¸ois Rabelais, 37200 Tours, France Correspondence should be addressed to F. Ruano; [email protected] Received 8 March 2013; Accepted 9 May 2013 Academic Editor: David P. Hughes Copyright © 2013 F. Ruano 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. The host-parasite genera Proformica-Rossomyrmex present four pairs of species with a very wide range of distribution from China to Southeastern Spain, from huge extended plains to the top of high mountains. Here we review (1) the published data on these pairs in comparison to other slave-makers; (2) the different dispersal ability in hosts and parasites inferred from genetics (chance of migration conditions the evolutionary potential of the species); (3) the evolutionary potential of host and parasite determining the coevolutionary process in each host-parasite system that we treat to define using cuticular chemical data. We find a lower evolutionary potential in parasites than in hosts in fragmented populations, where selective pressures give advantage to a limited female parasite migration due to uncertainty of locating a host nest. -
The Evolution of Social Parasitism in Formica Ants Revealed by a Global Phylogeny – Supplementary Figures, Tables, and References
The evolution of social parasitism in Formica ants revealed by a global phylogeny – Supplementary figures, tables, and references Marek L. Borowiec Stefan P. Cover Christian Rabeling 1 Supplementary Methods Data availability Trimmed reads generated for this study are available at the NCBI Sequence Read Archive (to be submit ted upon publication). Detailed voucher collection information, assembled sequences, analyzed matrices, configuration files and output of all analyses, and code used are available on Zenodo (DOI: 10.5281/zen odo.4341310). Taxon sampling For this study we gathered samples collected in the past ~60 years which were available as either ethanol preserved or pointmounted specimens. Taxon sampling comprises 101 newly sequenced ingroup morphos pecies from all seven species groups of Formica ants Creighton (1950) that were recognized prior to our study and 8 outgroup species. Our sampling was guided by previous taxonomic and phylogenetic work Creighton (1950); Francoeur (1973); Snelling and Buren (1985); Seifert (2000, 2002, 2004); Goropashnaya et al. (2004, 2012); Trager et al. (2007); Trager (2013); Seifert and Schultz (2009a,b); MuñozLópez et al. (2012); Antonov and Bukin (2016); Chen and Zhou (2017); Romiguier et al. (2018) and included represen tatives from both the New and the Old World. Collection data associated with sequenced samples can be found in Table S1. Molecular data collection and sequencing We performed nondestructive extraction and preserved samespecimen vouchers for each newly sequenced sample. We remounted all vouchers, assigned unique specimen identifiers (Table S1), and deposited them in the ASU Social Insect Biodiversity Repository (contact: Christian Rabeling, [email protected]).