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Radiation in Socially Parasitic Formicoxenine Ants
RADIATION IN SOCIALLY PARASITIC FORMICOXENINE ANTS DISSERTATION ZUR ERLANGUNG DES DOKTORGRADES DER NATURWISSENSCHAFTEN (D R. R ER . N AT .) DER NATURWISSENSCHAFTLICHEN FAKULTÄT III – BIOLOGIE UND VORKLINISCHE MEDIZIN DER UNIVERSITÄT REGENSBURG vorgelegt von Jeanette Beibl aus Landshut 04/2007 General Introduction II Promotionsgesuch eingereicht am: 19.04.2007 Die Arbeit wurde angeleitet von: Prof. Dr. J. Heinze Prüfungsausschuss: Vorsitzender: Prof. Dr. S. Schneuwly 1. Prüfer: Prof. Dr. J. Heinze 2. Prüfer: Prof. Dr. S. Foitzik 3. Prüfer: Prof. Dr. P. Poschlod General Introduction I TABLE OF CONTENTS GENERAL INTRODUCTION 1 CHAPTER 1: Six origins of slavery in formicoxenine ants 13 Introduction 15 Material and Methods 17 Results 20 Discussion 23 CHAPTER 2: Phylogeny and phylogeography of the Mediterranean species of the parasitic ant genus Chalepoxenus and its Temnothorax hosts 27 Introduction 29 Material and Methods 31 Results 36 Discussion 43 CHAPTER 3: Phylogenetic analyses of the parasitic ant genus Myrmoxenus 46 Introduction 48 Material and Methods 50 Results 54 Discussion 59 CHAPTER 4: Cuticular profiles and mating preference in a slave-making ant 61 Introduction 63 Material and Methods 65 Results 69 Discussion 75 CHAPTER 5: Influence of the slaves on the cuticular profile of the slave-making ant Chalepoxenus muellerianus and vice versa 78 Introduction 80 Material and Methods 82 Results 86 Discussion 89 GENERAL DISCUSSION 91 SUMMARY 99 ZUSAMMENFASSUNG 101 REFERENCES 103 APPENDIX 119 DANKSAGUNG 120 General Introduction 1 GENERAL INTRODUCTION Parasitism is an extremely successful mode of life and is considered to be one of the most potent forces in evolution. As many degrees of symbiosis, a phenomenon in which two unrelated organisms coexist over a prolonged period of time while depending on each other, occur, it is not easy to unequivocally define parasitism (Cheng, 1991). -
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 (Hymenoptera: 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. -
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. -
Cuticular Hydrocarbon Profiles in the Slave-Making
sympatrically in parts of Europe [13]. thank Nitto Electric Co. for providing 5. Dyer, L. J., et al.: Can. Ent. 114, 891 Although the sex pheromone of the for- the synthetic S-enantiomer. (1982) mer was estimated to be 100% (+)- 6. Schneider, D.: Naturwissenschaften 79, 241 (1992) dispalure, the gypsy moth possesses cells Received Novemer 11, 1992 and February 7. Inouchi, J., et al.: Int. J. Insect Mor- 8, 1993 specialized to (+)- and (-)-dispalure (a phol. Embryol 16, 177 (1982) pheromone inhibitor), whereas in the 8. Meinecke, C.-C.: Zoomorphologie 82, nun moth, which was estimated to uti- 1 (1975) lize 90% (-)-, and 10% (+)-dispalure, 9. Kafka, W. A., et al. : J. Comp. Physiol. both cells responded to (+)-dispalure 1. Bestmann, H. J., Vostrowsky, O.: CRC 87, 277 (1973) and no (-)-dispalure-sensitive cell was Handbook of Natural Pesticides, Vol. 10. Leal, W. S., et al.: J. Chem. Ecol. (in found. 4A. Boca Raton: CRC Press 1988 press) 2. Tumlinson, J. H., et al.: Science 197, 11. Fukusaki, E., et al.: Biosci. Biotech. We are grateful to K. Asaoka, Dr. A. 789 (1977) Biochem. 56, 1160 (1992) Sen, and Dr. J. Inouchi for advice 3. Leal, W. S., et al.: Naturwissenschaften 12. Okada, K., et al. : J. Insect Physiol. 38, regarding the preparations of samples 78, 521 (1991) 705 (1992) for SEM and TEM as well as for their 4. Cuperus, R L.: Int. J. Insect Morphol. 13. Hansen, K., et al.: Naturwissenschaf- critical review of the manuscript. We Embryol. 14, 347 (1985) ten 70, 466 (1983) Naturwissenschaften 80, 281-285 (1993) © Springer-Verlag 1993 suggested that slave-makers chemically mark their slaves to prevent them from returning to their own colonies [9]. -
Of Hungary: Survey of Ant Species with an Annotated Synonymic Inventory
insects Article The Myrmecofauna (Hymenoptera: Formicidae) of Hungary: Survey of Ant Species with an Annotated Synonymic Inventory Sándor Cs˝osz 1,2, Ferenc Báthori 2,László Gallé 3,Gábor L˝orinczi 4, István Maák 4,5, András Tartally 6,* , Éva Kovács 7, Anna Ágnes Somogyi 6 and Bálint Markó 8,9 1 MTA-ELTE-MTM Ecology Research Group, Pázmány Péter sétány 1/C, 1117 Budapest, Hungary; [email protected] 2 Evolutionary Ecology Research Group, Centre for Ecological Research, Institute of Ecology and Botany, 2163 Vácrátót, Hungary; [email protected] 3 Department of Ecology and Natural History Collection, University of Szeged, Szeged Boldogasszony sgt. 17., 6722 Szeged, Hungary; [email protected] 4 Department of Ecology, University of Szeged, Közép fasor 52, 6726 Szeged, Hungary; [email protected] (G.L.); [email protected] (I.M.) 5 Museum and Institute of Zoology, Polish Academy of Sciences, ul. Wilcza 64, 00-679 Warsaw, Poland 6 Department of Evolutionary Zoology and Human Biology, University of Debrecen, Egyetem tér 1, 4032 Debrecen, Hungary; [email protected] 7 Kiskunság National Park Directorate, Liszt F. u. 19, 6000 Kecskemét, Hungary; [email protected] 8 Hungarian Department of Biology and Ecology, Babe¸s-BolyaiUniversity, Clinicilor 5-7, 400006 Cluj-Napoca, Romania; [email protected] 9 Centre for Systems Biology, Biodiversity and Bioresources, Babes, -Bolyai University, Clinicilor 5-7, 400006 Cluj-Napoca, Romania * Correspondence: [email protected]; Tel.: +36-52-512-900 (ext. 62349) Simple Summary: Abundance is a hallmark of ants (Hymenoptera: Formicidae). They are exceed- ingly common in both natural and artificial environments and they constitute a conspicuous part Citation: Cs˝osz,S.; Báthori, F.; Gallé, of the terrestrial ecosystem; every 3 to 4 out of 10 kg of insects are given by ants. -
The Evolution of Social Parasitism in Formica Ants Revealed by a Global Phylogeny
bioRxiv preprint doi: https://doi.org/10.1101/2020.12.17.423324; this version posted February 15, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. The evolution of social parasitism in Formica ants revealed by a global phylogeny Marek L. Borowiec*a,b,c, Stefan P. Coverd, and Christian Rabeling†a aSchool of Life Sciences, Arizona State University, Tempe, AZ 85287, U.S.A. bInstitute of Bioinformatics and Evolutionary Studies (IBEST), University of Idaho, Moscow, ID 83843, U.S.A. cDepartment of Entomology, Plant Pathology and Nematology, University of Idaho, Moscow, ID 83844, U.S.A. dMuseum of Comparative Zoology, Harvard University, Cambridge, MA 02138, U.S.A. Abstract Studying the behavioral and life history transitions from a cooperative, eusocial life history to exploita tive social parasitism allows for deciphering the conditions under which changes in behavior and social organization lead to diversification. The Holarctic ant genus Formica is ideally suited for studying the evo lution of social parasitism because half of its 176 species are confirmed or suspected social parasites, which includes all three major classes of social parasitism known in ants. However, the lifehistory transitions associated with the evolution of social parasitism in this genus are largely unexplored. To test compet ing hypotheses regarding the origins and evolution of social parasitism, we reconstructed the first global phylogeny of Formica ants and representative formicine outgroups. -
First Record of the Permanent Social Parasitic, Slavemaking Ant Harpagoxenus Sublaevis (NYLANDER, 1852) for Belgium (Hymenoptera, Formicidae)
~ Bulletin S.R.B.E.IK.B.V.E., 142 (2006): 21-24 First record of the permanent social parasitic, slavemaking ant Harpagoxenus sublaevis (NYLANDER, 1852) for Belgium (Hymenoptera, Formicidae) Peter BOER 1 & Wouter DEKONINC~ 1 Gemene Bos 12, 1861 HG Bergen, The Netherlands (e-mail: [email protected]). 2 Royal Belgian Institute of Natural Sciences, Department Entomology, Vautierstraat 29, B-1000 Brussels, Belgium. Abstract We report the first record of the permanent parasitic ant Harpagoxenus sublaevis (NYLANDER, 1852) in Belgium. A nest of the species was discovered on 3.V.2006 in Nahtsief in the Hautes Fagnes. In the nest workers of its frequently used host Leptothorax acervorum (F ABRICJUS, 1793) were found. This paper presents the locality, coexisting ant fauna and possibilities where to rediscover this species. Keywords: first record, Belgium, Harpagoxenus sublaevis, faunistic. Resume Nous signalons la premiere capture d 'Harpagoxenus sublaevis (NYLANDER, 1852) une fo urmi esclavagisteobligatoire en Belgique. Un nid de cette espece a ete trouve le 3.V.2006 a Nahtsiefdans les Hautes Fagnes, dans lequel se trouvaient egalement des ouvrieres de Leptothorax acervorum (FABRICIUS, 1793), une des especes cibles d'Harpagoxenus sublaevis. Ici on commente la localite, les differentes fourmis avoisinantes et les possibilites de retrouver 1'es pece en Belgique. Samenvatting We melden hier de eerste waam eming van de permanent, parasitaire slavenjaagster Ha1pagoxenus sublaevis (NYLANDER, 1852), de nijptangmier in Belgie. Een nest van deze soort werd ontdekt op 3.V.2006 in Nahtsief in de Hoge Venen. In het nest werden ook werksters van de vaak door deze soort gebruikte gastheer Leptothorax acervorum (FABRJCJUS, 1793) gevonden. -
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). -
The Evolution of Social Parasitism in Formica Ants Revealed by a Global Phylogeny
bioRxiv preprint doi: https://doi.org/10.1101/2020.12.17.423324; this version posted December 21, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. The evolution of social parasitism in Formica ants revealed by a global phylogeny Marek L. Borowiec*a,b,d, Stefan P. Coverc, and Christian Rabeling†a aSchool of Life Sciences, Arizona State University, Tempe, AZ 85287, U.S.A. bInstitute of Bioinformatics and Evolutionary Studies (IBEST), University of Idaho, Moscow, ID 83843, U.S.A. cMuseum of Comparative Zoology, Harvard University, Cambridge, MA 02138, U.S.A. dCurrent address: Department of Entomology, Plant Pathology and Nematology, University of Idaho, Moscow, ID 83844, U.S.A. Abstract Studying the behavioral and life history transitions from a cooperative, eusocial life history to exploita tive social parasitism allows for deciphering the conditions under which changes in behavior and social organization lead to diversification. The Holarctic ant genus Formica is ideally suited for studying the evo lution of social parasitism because half of its 178 species are confirmed or suspected social parasites, which includes all three major classes of social parasitism known in ants. However, the lifehistory transitions associated with the evolution of social parasitism in this genus are largely unexplored. To test compet ing hypotheses regarding the origins and evolution of social parasitism, we reconstructed the first global phylogeny of Formica ants and representative formicine outgroups. -
Leptothorax Wilsoni N. Sp., a New Parasitic Ant from Eastern North America (Hymenoptera: Formicidae)* by J
LEPTOTHORAX WILSONI N. SP., A NEW PARASITIC ANT FROM EASTERN NORTH AMERICA (HYMENOPTERA: FORMICIDAE)* BY J. HEINZE Museum of Comparative Zoology, Harvard University Cambridge, Mass. 02138, USA Wherever populations of ants are dense, social parasitic species can occur. Parasitic ants are dependent on workers of another spe- cies for all or a portion of their life-cycle. They often exhibit fasci- nating behaviors such as slave-raids, e.g. in Polyergus rufescens and Harpagoxenus sublaevis, the throttling or decapitation of host queens by Epimyrma or Bothriomyrmex respectively, or riding like an ectoparasite on the back of the host queen in Teleutomyrmex schneideri (Wilson, 1971; Buschinger, 1987). Social parasites are unusually common in the myrmicine tribe Leptothoracini. For example, Leptothorax acervorum, an ant common in alpine and boreal forests throughout northern and cen- tral Europe, is host to four different parasitic species: the slave- maker Harpagoxenus sublaevis and the workerless Doronomyrnex goesswaldi, D. kutteri, and D. pacis (Buschinger, 1971). In North America, however, the vast populations of several species closely related to L. acervorum (currently synonymized under L. "musco- rum"by Brown, 1955), are parasitized only by Harpagoxenus cana- densis in the northeast (Creighton, 1950)and the inquiline L.faberi, known only from its type locality in Alberta (Buschinger, 1981). The status of a third species, Doronomyrmex pocahontas, formerly thought to be a workerless parasite (Buschinger, 1979), is unclear (Heinze and Buschinger, unpubl, data). In this paper I report findings of a new, apparently workerless parasitic Leptothorax from Mount Monadnock, Cheshire Co., New Hampshire. The new parasite has small, brachypterous queens characterized by an alitrunk notably reduced in size. -
The Journey of Tandem Running: the Twists, Turns and What We Have Learned
Insect. Soc. (2014) 61:1–8 DOI 10.1007/s00040-013-0325-3 Insectes Sociaux REVIEW ARTICLE The journey of tandem running: the twists, turns and what we have learned E. L. Franklin Received: 4 February 2013 / Revised: 28 October 2013 / Accepted: 4 November 2013 / Published online: 21 November 2013 Ó International Union for the Study of Social Insects (IUSSI) 2013 Abstract Tandem running, whereby one worker recruits acquired slave workers back to the slaver’s home nest another is utilised by many ant species. Since first being (Buschinger et al., 1980). recorded, it has provided a valuable experimental tool for Wilson (1959) described tandem running, in the ant testing hypotheses about collective decision making, com- genus Cardiocondyla, as a communication method used munication and even teaching. In this review I explore the by workers to recruit others to food sources. This method journey tandem running has taken, the twists and turns in the of communication differed from the pheromone mass theories surrounding it and what tandem running has taught recruitment, trail laying behaviour used by worker ants to us. This review examines the empirical research conducted recruit other workers (Wilson, 1971). Foraging trails are on tandem running, from when it was first described, con- created when on finding a food source, a worker leaves a siders the theories that have arisen from that research and pheromone trail from it back to the nest. The trail stim- ultimately what has been learnt and what is still yet to be ulates other workers to follow the trail to the food source. -
Sociobiology 68(3): E7224 (September, 2021) DOI: 10.13102/Sociobiology.V68i3.7224
Sociobiology 68(3): e7224 (September, 2021) DOI: 10.13102/sociobiology.v68i3.7224 Sociobiology An international journal on social insects REsearch ARtIClE - ANts First Record of the Inquiline Ant Leptothorax kutteri Buschinger, 1965 from Turkey Kadri Kiran1, Celal Karaman1, Jürgen Heinze2 1- Department of Biology, Trakya University, Edirne, Turkey 2- Zoology/Evolutionary Biology, University of Regensburg, Regensburg, Germany Article History Abstract We report on the occurrence of the ant Leptothorax kutteri Edited by Evandro Nascimento Silva, UEFS, Brazil Buschinger, 1965 in two sites in Northern and Eastern Turkey. Received 18 May 2021 Leptothorax kutteri is a workerless inquiline living in the colonies of Initial acceptance 07 July 2021 L. acervorum (Fabricius, 1793) so far known from various parts of Final acceptance 08 July 2021 Northern and Central Europe. Our findings greatly increase the range Publication date 13 August 2021 of this small and rare ant. Keywords Inquilinism, social parasitism, biodiversity. Corresponding author Kadri Kiran Trakya University, Department of Biology, Faculty of Science 22030, Edirne, Turkey. E-Mail: [email protected] Introduction host populations, and spotting the few inquiline queens among the host ants is often difficult. Our knowledge about Ant societies typically are protected against intruders the occurrence and distribution of inquilines is therefore or parasites through a highly efficient system of nestmate incomplete and novel findings are worth of being mentioned. recognition. Nevertheless, numerous species of arthropods and We here report on the occurrence of Leptothorax other animals have evolved mechanisms of invading the nests of kutteri Buschinger, 1965 (previously also referred to as ants by masking themselves with or mimicking the recognition Doronomyrmex kutteri) from two sites in Northern and cues of their hosts.