Hymenoptera: Formicidae) of Hungary: an Updated Checklist

Total Page:16

File Type:pdf, Size:1020Kb

Hymenoptera: Formicidae) of Hungary: an Updated Checklist NORTH-WESTERN JOURNAL OF ZOOLOGY 7 (1): pp.55-62 ©NwjZ, Oradea, Romania, 2011 Article No.: 111104 www.herp-or.uv.ro/nwjz The myrmecofauna (Hymenoptera: Formicidae) of Hungary: an updated checklist Sándor CSŐSZ1,*, Bálint MARKÓ2 & László GALLÉ3 1. Hymenoptera Collection, Hungarian Natural History Museum, str. Baross 13, 1088 Budapest, Hungary, E-mail: [email protected] 2. Department of Taxonomy and Ecology, Babeş-Bolyai University, str. Clinicilor 5-7, 400006 Cluj-Napoca, Romania, E-mail: [email protected] 3. Department of Ecology, University of Szeged, P.O. Box 51, 6701 Szeged, Hungary, E-mail: [email protected] * Corresponding author, S. Csősz, e-mail: [email protected] Received: 22. July 2010 / Accepted: 18. January 2011 / Available online: 25. January 2011 Abstract. The last checklist of Hungarian myrmecofauna was published at the end of the 1990s. Since then, several taxonomic and faunistic changes have occurred. The following article provides an updated checklist of Hungarian ants containing 126 species, five of which are found exclusively indoors. Six new species of the Hungarian myrmecofauna are reported (Temnothorax albipennis, T. jailensis, Tetramorium sp. D, Tapinoma melanocephalum, Plagiolepis pallescens, and P. ampeloni), and a few species are deleted from the list. Finally, we offer a brief descriptive comparison of the Hungarian myrmecofauna with the ant fauna of the surrounding countries. Keywords: ants, faunistics, checklist, Hungary, Europe. Introduction the 20th century (e.g. Gallé 1969, 1972, 1979, Gallé & Szőnyi 1988, Csősz & Tartally 1998). The myrmecofauna of central and eastern Europe However, since publication of the most recent is relatively well-known. Over the course of the Hungarian checklist, many new taxa have been past few decades several old checklists and described (e.g. Seifert 2003, Schlick-Steiner et al. faunistic monographs have been updated and new 2006, Csősz et al. 2007, Csősz & Schulz 2010), ones have been published for central and eastern revived from synonymy (e.g. Csősz & Seifert 2003, Europe countries (e.g. Radchenko 1991, Seifert Radchenko & Elmes 2009), or the validity of their 2001, Czechowski et al. 2002, Steiner et al. 2002, status has been confirmed on the basis of new Karaman 2004, Radchenko et al. 2004, Bračko 2006, findings (Csősz & Markó 2004). Furthermore, 2007, Petrov 2006, Werner & Wiezik 2007, several new myrmecological studies have been Karaman 2009, Lapeva-Gjonova et al. 2010). The carried out reporting new ant species for the last checklist of Hungarian ants was compiled in Hungarian fauna and new data regarding species the late 1990s and reported 101 species (Gallé et al. already known (e.g. Csősz 2000, 2001, 2003, Csősz 1998). et al. 2002, Markó & Csősz 2002, , Tartally & Csősz The myrmecofauna of present-day Hungary 2004, Csősz & Markó 2005, Gallé et al. 2005, Csősz has been studied in considerable detail over the et al. 2007, Ionescu-Hirsch et al. 2009, Csősz & course of the last few centuries, and several Schulz 2010). Consequently, there is need of an checklists have been published since the mid updated checklist of the Hungarian myrmeco- 1800’s. The first detailed checklist containing fauna such as the one presented here. locations was published by Mayr (1856). He listed 40 species for the territory of present-day Hungary. His work was later updated toward the Materials and methods end of the 19th century (Mocsáry 1897) resulting in a checklist that contained 56 species for the The current species list was prepared by consulting major myrmecofaunistic papers for the territory of current territory of present-day Hungary. His work was Hungary, as well as other papers handling Hungarian followed by Somfai’s (1959) monograph that listed data. The list of names was based on the catalogue by 66 species. Thus, the number of species increased Bolton et al. (2006), as well as on the basis of currently considerably in the last checklist of Hungarian available taxonomic literature (e.g. Czechowski et al. ants (Gallé et al. 1998), due mostly to intensive 2002, Seifert 2007, Radchenko & Elmes 2009). In some myrmecological work during the second half of cases the Antbase search engine (Agosti & Johnson 2005) 56 Csősz, S. et al. was also used. Most species were collected in recent Myrmica deplanata Ruzsky, 1905: Somfai (1959) decades, but some records could not be verified by Myrmica gallienii Bondroit, 1920: Csősz & Tartally checking voucher specimens or by collecting from sample (1998) sites. Among respective species, those not recorded from Myrmica karavajevi (Arnoldi, 1930) surrounding countries or those with unclear taxonomic status at the time of publication were considered of = Sifolinia karavajevi: Gallé et al. (1998) uncertain occurrence in Hungary. = Sifolinia faniensis (van Boven, 1970): Gallé (1979) Myrmica lobicornis Nylander, 1846: Mocsáry (1897) List of species Myrmica lonae Finzi, 1926: Tartally & Csősz (2004) Myrmica rubra (Linnaeus, 1758): Csősz & Tartally A total of 125 species were recorded from Hun- (1998) gary, including six new species: Temnothorax albi- = Myrmica laevinodis Nylander, 1846: Mayr pennis, T. jailensis, Tetramorium sp. D, Tapinoma (1856) melanocephalum, Plagiolepis pallescens, and P. = Myrmica microrubra Seifert, 1993: Csősz et al. ampeloni. Five species of exotic origin were record- (2002) ed exclusively from indoors: Hypoponera puncta- Myrmica ruginodis Nylander, 1846: Mayr (1855) tissima, Monomorium pharaonis, Tetramorium bicari- Myrmica rugulosa Nylander, 1849: Mocsáry (1897) natum, T. insolens, and Tapinoma melanocephalum. Myrmica sabuleti Meinert, 1861: Somfai (1959) Four species were considered of uncertain occur- Myrmica scabrinodis Nylander, 1846: Mayr (1855) rence: Myrmica sulcinodis, Camponotus sylvaticus, = Myrmica rugulosoides Forel, 1915: Gallé (1967) Formica aquilonia, and F. lugubris, and were Myrmica schencki Viereck, 1903: Gallé (1986a) excluded from the list of Hungarian myrmeco- Myrmica slovaca Sadil, 1952 - M. slovaca has been fauna. generally misidentified as M. salina in central Europe, while M. salina occurs closest in Subfamily Proceratiinae Kazakhstan (Radchenko & Elmes 2009). Proceratiini = Myrmica salina Ruzsky, 1905: Csősz & Proceratium melinum (Roger, 1860) Tartally (1998) = Sysphincta fialai Kratochvil, 1944: Somfai (1959) Myrmica specioides Bondroit, 1918: Gallé (1975) = Myrmica sancta Karavaiev, 1926: Gallé Subfamily Ponerinae (1972b) Ponerini Myrmica vandeli Bondroit, 1920: Tartally & Csősz Cryptopone ochracea (Mayr, 1855) (2004) = Cryptopone ochraceum: Csősz (2003) Myrmecinini Hypoponera punctatissima (Roger, 1859): Gallé et al. Myrmecina graminicola (Latreille, 1802): Somfai (1998) (1959) = Ponera punctatissima: Somfai (1959) = Myrmecina latreillei Curtis, 1829: Mayr (1856) Ponera coarctata (Latreille, 1802): Mayr (1856) Ponera testacea Emery, 1895: Csősz & Seifert (2003) Pheidolini Aphaenogaster subterranea (Latreille, 1798): Mocsáry Subfamily Myrmicinae (1897) Dacetini Messor structor (Latreille, 1798): Somfai (1959) Pyramica argiola (Emery, 1869) = Atta structor: Mayr (1855) = Epitritus argiolus: Mocsáry (1897) = Aphaenogaster structor: Mocsáry (1897) Pyramica baudueri (Emery, 1875) = Messor rufitarsus (Fabricius 1804): Gallé = Strumigenys baudueri: Somfai (1959) (1986b) = Smithistruma baudueri: Gallé et al. (1998) Stenammini Myrmicini Stenamma debile (Foerster, 1850): Csősz (2000) Manica rubida (Latreille, 1802): Gallé et al. (1998) = Stenamma westwoodii Westwood, 1839: = Myrmica rubida: Mayr 1855 Somfai (1959) = Myrmica (Neomyrma) rubida: Somfai (1959) Crematogastrini Myrmica constricta Karavajev, 1934 Crematogaster schmidti (Mayr, 1853): Gallé et al. = Myrmica hellenica Finzi, 1926: Gallé et al. (1998) (2005) The myrmecofauna of Hungary 57 Crematogaster scutellaris (Olivier, 1792): Mayr Temnothorax rabaudi (Bondroit, 1918) (1861) = Leptothorax rabaudi Bondroit, 1918: Barrett Crematogaster sordidula (Nylander, 1849): Mayr (1970) (1861) Temnothorax sordidulus (Müller, 1923) = Leptothorax sordidulus: Csősz (2001) Solenopsidini Temnothorax tuberum (Fabricius, 1775) Monomorium pharaonis (Linnaeus, 1758): Somfai = Leptothorax tuberum: Mayr 1855: Mayr (1861) (1959) Temnothorax unifasciatus (Latreille, 1798) Solenopsis fugax (Latreille, 1798): Mayr (1856) = Leptothorax unifasciatus: Mayr (1856) Formicoxenini = Leptothorax tuberum var. unifasciatus: André Formicoxenus nitidulus (Nylander, 1846): Somfai 1881: Somfai (1959) (1959) Tetramoriini Harpagoxenus sublaevis (Nylander, 1849): Somfai Anergates atratulus (Schenck, 1952): Mocsáry (1897) (1959) = Tetramorium atratulum: Mayr (1856) Myrmoxenus ravouxi (André, 1896) Strongylognathus testaceus (Schenck, 1952): Mayr = Epimyrma goesswaldi Menozzi, 1930: Gallé & (1856) Szőnyi (1988) Tetramorium bicarinatum (Nylander, 1846): = Epimyrma ravouxi: Csősz & Tartally (1998) Mocsáry (1897) Cardiocondyla elegans Emery, 1869 Tetramorium caespitum (Linnaeus, 1758): Mayr = Cardiocondyla sahlbergi Forel, 1913: Gallé et (1855) al. (1998) [erroneous determination] Tetramorium ferox Ruzsky, 1903: Radchenko (1977) Leptothorax acervorum (Fabricius, 1783): Somfai Tetramorium hungaricum Röszler, 1935 (1959) = Tetramorium caespitum hungaricum Röszler, Leptothorax gredleri Mayr, 1855: Somfai (1959) 1935: 78. Röszler (1935) Leptothorax muscorum (Nylander, 1846): Somfai = Tetramorium hungaricum: Röszler (1951) (1959) Tetramorium impurum (Förster, 1850): Csősz et al. Temnothorax affinis (Mayr, 1855) (2002) = Leptothorax affinis Mayr, 1855: Somfai (1959) Tetramorium
Recommended publications
  • Iberomyrmex 7 2015.Pdf
    Asociación Ibérica de Mirmecología , diciembre 2015 ISSN 1989-7928 Asociación Ibérica de Mirmecología Iberomyrmex nº 7 www.mirmiberica.org Iberomyrmex. Número 7, diciembre 2015 IBEROMYRMEX Boletín de la Asociación Ibérica de Mirmecología Publicación anual de acceso gratuito. Disponible en “http://www.mirmiberica.org/iberomyrmex” Número 7. Fecha: 31 de diciembre de 2015. Asociación Ibérica de Mirmecología “www.mirmiberica.org” ISSN 1989-7928 Título clave: Iberomyrmex Tít. abreviado: Iberomyrmex Diseño y maquetación del presente volumen: Amonio David Cuesta Segura, excepto portada y contraportada: Natalia Arnedo Rodríguez. Editor del presente volumen: Sílvia Abril Meléndez. Asesor lingüístico: Pedro Peña Varó. Revisores de los trabajos del presente volumen (por orden alfabético de los apellidos): Sílvia Abril, Xavier Espadaler, Crisanto Gómez y Joaquín Reyes. Nota de copyright © AIM, 2015; © Los autores, 2015; Los originales publicados en la edición electrónica de Iberomyrmex son propiedad de la Asociación Ibérica de Mirmecología y de los propios autores, siendo necesario citar la procedencia en cualquier reproducción parcial o total. Salvo que se indique lo contrario, todos los contenidos de la edición electrónica se distribuyen bajo una licencia de uso y distribución “Creative Commons Reconocimiento- No Comercial 3.0 España” (CC-by-nc). Puede consultar desde aquí la versión informativa y el texto legal de la licencia. Esta circunstancia ha de hacerse constar expresamente de esta forma cuando sea necesario. Normas de publicación: http://www.mirmiberica.org/iberomyrmex Envío de manuscritos: “[email protected]” Los autores se responsabilizan de las opiniones contenidas en los artículos y comunicaciones. Artículos y notas Artículos y notas Artículos y notas Artículos y notas Artículos y notas Artículos y notas Artículos y notas Artículos Artículos y notasy notas Artículos y notas Artículos Iberomyrmex.
    [Show full text]
  • Ants Inhabiting Oak Cynipid Galls in Hungary
    North-Western Journal of Zoology 2020, vol.16 (1) - Correspondence: Notes 95 Ants inhabiting oak Cynipid galls in Hungary Oaks are known to harbour extremely rich insect communi- ties, among them more than 100 species of gall wasps (Hy- menoptera: Cynipidae) in Europe (Csóka et al. 2005, Melika 2006). Some gall wasp species are able to induce large and structurally complex galls that can sometimes be abundant on oaks, providing attractive shelters for several arthropod taxa including ant species. Ants are among the most important players in many ecosystems and they are also considered to act as ecosystem engineers (Folgarait, 1998). They are also famous for having ecological or physical interactions with a great variety of other organisms, such as gall wasps. Ants are known to tend Figure 1. Inner structure of the asexual Andricus quercustozae gall in- aphid colonies on the developing galls and, as general pred- habited by ants. ators, they prey on arthropods approaching the protected aphid colonies. Some oak cynipid galls secrete honeydew on their surface. This sweet substrate attracts ants and, in re- turn, the ants protect the galls from predators and parasi- toids (Abe, 1988, 1992; Inouye & Agrawal 2004; Nicholls, 2017). Beyond this obvious ecological interaction between gall wasps and ants, this association continues after the gall wasp’s life cycle has ceased. Certain galls are known to serve as either temporary or permanent shelter for many ant species. Some galls (e.g. An- dricus hungaricus (Hartig), Andricus quercustozae (Bosc), Aphelonyx cerricola (Giraud)) are large enough even for re- productive ant colonies. The advantages of galls as nesting logs are multifaceted.
    [Show full text]
  • This Article Appeared in a Journal Published by Elsevier. the Attached
    This article appeared in a journal published by Elsevier. The attached copy is furnished to the author for internal non-commercial research and education use, including for instruction at the authors institution and sharing with colleagues. Other uses, including reproduction and distribution, or selling or licensing copies, or posting to personal, institutional or third party websites are prohibited. In most cases authors are permitted to post their version of the article (e.g. in Word or Tex form) to their personal website or institutional repository. Authors requiring further information regarding Elsevier’s archiving and manuscript policies are encouraged to visit: http://www.elsevier.com/copyright Author's personal copy Ecological Indicators 13 (2012) 303–313 Contents lists available at ScienceDirect Ecological Indicators jo urnal homepage: www.elsevier.com/locate/ecolind Life-history strategies as a tool to identify conservation constraints: A case-study ଝ on ants in chalk grasslands a,b,∗ c d a,b,1 C.G.E. (Toos) van Noordwijk , Peter Boer , A.A. (Bram) Mabelis , Wilco C.E.P. Verberk , b,d Henk Siepel a Bargerveen Foundation, Toernooiveld 1, 6525 ED Nijmegen, The Netherlands b Department of Animal Ecology and Ecophysiology, Institute of Water and Wetland Research, Radboud University Nijmegen, P.O. Box 9010, 6500 GL Nijmegen, The Netherlands c Gemene Bos 12, 1861 HG Bergen, The Netherlands d Centre for Ecosystem Studies, Alterra, Wageningen UR, P.O. Box 47, 6700 AA Wageningen, The Netherlands a r t i c l e i n f o a b s t r a c t Article history: Species’ life-history traits underlie species–environment relationships.
    [Show full text]
  • Succession in Ant Communities (Hymenoptera: Formicidae) in Deciduous Forest Clear-Cuts – an Eastern European Case Study
    EUROPEAN JOURNAL OF ENTOMOLOGYENTOMOLOGY ISSN (online): 1802-8829 Eur. J. Entomol. 114: 92–100, 2017 http://www.eje.cz doi: 10.14411/eje.2017.013 ORIGINAL ARTICLE Succession in ant communities (Hymenoptera: Formicidae) in deciduous forest clear-cuts – an Eastern European case study IOAN TĂUŞAN 1, JENS DAUBER 2, MARIA R. TRICĂ1 and BÁLINT MARKÓ 3 1 Department of Environmental Sciences, Lucian Blaga University of Sibiu; Applied Ecology Research Centre, Dr. Raţiu 5-7, 550012 Sibiu, Romania; e-mails: [email protected], [email protected] 2 Thünen Institute of Biodiversity, Federal Research Institute for Rural Areas, Forestry and Fisheries, Bundesallee 50, D-38116 Braunschweig, Germany; e-mail: [email protected] 3 Hungarian Department of Biology and Ecology, Babeş-Bolyai University, Clinicilor 5-7, 400006 Cluj-Napoca, Romania; e-mails: [email protected], [email protected] Key words. Hymenoptera, Formicidae, ants, deciduous forests, secondary succession, clear-cutting, community structure, pitfall traps Abstract. Clear-cutting, the main method of harvesting in many forests in the world, causes a series of dramatic environmental changes to the forest habitat and removes habitat resources for arboreal and epigeal species. It results in considerable changes in the composition of both plant and animal communities. Ants have many critical roles in the maintenance and functioning of forest ecosystems. Therefore, the response of ants to clear-cutting and the time it takes for an ant community to recover after clear- cutting are important indicators of the effect of this harvesting technique on the forest ecosystem. We investigated ground-dwelling ant communities during secondary succession of deciduous forests in Transylvania, Romania.
    [Show full text]
  • 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).
    [Show full text]
  • Taxonomic Revision of the Cretan Fauna of the Genus Temnothorax Mayr, 1861 (Hymenoptera: Formicidae), with Notes on the Endemism of Ant Fauna of Crete
    ANNALES ZOOLOGICI (Warszawa), 2018, 68(4): 769-808 TAXONOMIC REVISION OF THE CRETAN FAUNA OF THE GENUS TEMNOTHORAX MAYR, 1861 (HYMENOPTERA: FORMICIDAE), WITH NOTES ON THE ENDEMISM OF ANT FAUNA OF CRETE SEBASTIAN SALATA1*, LECH BOROWIEC2, APOSTOLOS TRICHAS3 1Institute for Agricultural and Forest Environment, Polish Academy of Sciences, Bukowska 19, 60-809 Poznań, Poland; e-mail: [email protected] 2Department of Biodiversity and Evolutionary Taxonomy, University of Wrocław, Przybyszewskiego 65, 51-148 Wrocław, Poland; e-mail: [email protected] 3Natural History Museum of Crete, University of Crete, Greece; e-mail: [email protected] *Corresponding author Abstract.— We revise the Cretan species of the ant genus Temnothorax Mayr, 1861. Sixteen species are recognized, including seven new species which are possiblyendemic to Crete: T. crassistriatus sp. nov., T. daidalosi sp. nov., T. ikarosi sp. nov., T. incompletus sp. nov., T. minotaurosi sp. nov., T. proteii sp. nov., and T. variabilis sp. nov. A new synonymy is proposed, Temnothorax exilis (Emery, 1869) =Temnothorax specularis (Emery, 1916) syn. nov. An identification key to Cretan Temnothorax, based on worker caste is given. We provide a checklist of ant species described from Crete and discuss their status, distribution and endemism. Ë Key words.— Key, checklist, Myrmicinae, new species, Mediterranean Subregion, new synonymy INTRODUCTION 2000 mm in the high White Mountains range (Lefka Ori) (Grove et al. 1993). Temperature on mountains Crete is the fifth largest island in the Mediterranean seems to fall at a rate of about 6°C per 1000 m (Rack- ham & Moody 1996). Above 1600 m most of the precipi- Sea and the biggest island of Greece.
    [Show full text]
  • Worldwide Spread of the Ruby Ant, Myrmica Rubra (Hymenoptera: Formicidae)
    Myrmecological News 14 87-96 Vienna, January 2011 Worldwide spread of the ruby ant, Myrmica rubra (Hymenoptera: Formicidae) James K. WETTERER & Alexander G. RADCHENKO Abstract The ruby ant, Myrmica rubra (LINNAEUS, 1758) (formerly Myrmica laevinodis NYLANDER, 1846), an aggressive Eur- asian species with a powerful sting, is now spreading through temperate North America. To document the worldwide distribution of M. rubra and evaluate its potential for further spread, we compiled published and unpublished specimen records from > 2000 sites. We report the earliest known M. rubra records for 71 geographic areas (countries, major is- lands, US states, Canadian provinces, and Russian federal districts), including three areas with no previously published records: Prince Edward Island, Washington State, and the Far Eastern Federal District of Russia. All earlier published records of M. rubra from East Asia, including the Far East of Russia, Japan, and China, appear to be misidentifications of Myrmica kotokui FOREL, 1911. Myrmica rubra is native to an enormous expanse extending from Ireland and Portugal in westernmost Europe across 8000 km to central Asia and eastern Siberia, and from 39 to 70° N in latitude. Exotic populations of M. rubra were first recorded in eastern North America more than 100 years ago. Myrmica rubra is now documented from five southeastern Canadian provinces (New Brunswick, Nova Scotia, Ontario, Prince Edward Island, and Quebec), six northeastern US states (Maine, Massachusetts, New Hampshire, New York, Rhode Island, and Vermont), and one northwestern state (Wash- ington) ranging from 41.5 to 47.6° N. Given the vast range of M. rubra in Eurasia, perhaps the most striking aspect about this species in North America is how little it has spread over the past century.
    [Show full text]
  • Download PDF File
    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.
    [Show full text]
  • Hazards for Nature? Avalanches As a Promotor of Biodiversity. a Case Study on the Invertebrate Fauna in the Gesäuse National Park (Styria, Austria)
    5th Symposium Conference Volume for Research in Protected Areas pages 389 - 398 10 to 12 June 2013, Mittersill Natural Hazards – Hazards for Nature? Avalanches as a promotor of biodiversity. A case study on the invertebrate fauna in the Gesäuse National Park (Styria, Austria) Christian Komposch, Thomas Frieß & Daniel Kreiner Abstract Avalanches are feared by humans and considered “catastrophic” due to their unpredictable and destructive force. But this anthropocentric perspective fails to capture the potential ecological value of these natural disturbances. The Gesäuse National Park is a model-region for investigations of such highly dynamic events because of its distinct relief and extreme weather conditions. This project aims to record and analyse the animal assemblages in these highly dynamic habitats as well as document succession and population structure. 1) Dynamic processes lead to one of the very few permanent and natural vegetationless habitat types in Central Europe outside the alpine zone – i. e. screes and other rocky habitats at various successional stages. In addition to the tight mosaic distribution of a variety of habitats over larger areas, avalanche tracks also offer valuable structures like dead wood and rocks. Remarkable is the sympatric occurrence of the three harvestmen species Trogulus tricarinatus, T. nepaeformis und T. tingiformis, a species diversity peak of spiders, true-bugs and ants; and the newly recorded occurrence of Formica truncorum. 2) The presence of highly adapted species and coenoses reflect the extreme environmental conditions, specific vegetation cover and microclimate of these habitats. Several of the recorded taxa are rare, endangered and endemic. The very rare dwarf spider Trichoncus hackmani is a new record for Styria and the stenotopic and critically endangered wolf-spider Acantholycosa lignaria is dependent on lying dead wood.
    [Show full text]
  • Myrmecophily of Maculinea Butterflies in the Carpathian Basin (Lepidoptera: Lycaenidae)
    ettudom sz án é y m ológia i r n i é e h K c a s T e r T Myrmecophily of Maculinea butterflies in the Carpathian Basin (Lepidoptera: Lycaenidae) A Maculinea boglárkalepkék mirmekofíliája a Kárpát- medencében (Lepidoptera: Lycaenidae) PhD Thesis Tartally András Department of Evolutionary Zoology and Human Biology University of Debrecen Debrecen, 2008. Ezen értekezést a Debreceni Egyetem TTK Biológia Tudományok Doktori Iskola Biodiverzitás programja keretében készítettem a Debreceni Egyetem TTK doktori (PhD) fokozatának elnyerése céljából. Debrecen, 2008.01.07. Tartally András Tanúsítom, hogy Tartally András doktorjelölt 2001-2005 között a fent megnevezett Doktori Iskola Biodiverzitás programjának keretében irányításommal végezte munkáját. Az értekezésben foglalt eredményekhez a jelölt önálló alkotó tevékenységével meghatározóan hozzájárult. Az értekezés elfogadását javaslom. Debrecen, 2008.01.07. Dr. Varga Zoltán egyetemi tanár In memory of my grandparents Table of contents 1. Introduction......................................................................................... 9 1.1. Myrmecophily of Maculinea butterflies........................................................ 9 1.2. Why is it important to know the local host ant species?.............................. 9 1.3. The aim of this study.................................................................................... 10 2. Materials and Methods..................................................................... 11 2.1. Taxonomy and nomenclature.....................................................................
    [Show full text]
  • Individual, Geographical and Experimental Variation of Cuticular
    Biochemical Systematics and Ecology,VoL 18, No. 1, pp. 63-73, 1990. 0305-1978/90 $3.00+0.00 Printed in GreatBritain. © 1990 Pergamon Press plc. Individual, Geographical and Experimental Variation of Cuticular Hydrocarbons of the Ant Cataglyphis cursor (Hymenoptera: Formicidae)" Their Use in Nest and Subspecies Recognition E. NOWBAHARI,* A. LENOIR,t J. L. CLI~MENT,:~ C. LANGE,§ A. G. BAGNERES$ and C. JOULIE$ *Laboratoire d'Ethologie et Psychophysiologie, Universit@ F. Rabelais, Parc de Grandmont, F-37200 Tours, France; lLaboratoire d'Ethologie et Sociobiologie, URA CNRS 661. Universit@ Paris Nord, Av. J. B. Cl@ment, F-93430 Villetaneuse, France; :~Laboratoire d'Evolution, Universit~ P. et M. Curie, 105 Bd Raspail, F-75006 Paris, France; §Laboratoire de Chimie Organique Structurale, UA CNRS 455. Universit@ P. et M. Curie, 4 place Jussieu, F-75005 Paris, France Key Word Index--Cataglyphis cursor; Hymenoptera; Formicidae; cuticle; hydrocarbons; colonial; odor; populations; aggressive behavior. Abstract--The cuticular hydrocarbons of Cataglyphis cursor (Fonsc.) adults have been identified and quantified. Comparison of the proportion of hydrocarbons in various locations shows a variation between populations from each side of the Rh6ne river and an isolated population in the mountains near Madrid. In the studied area (not including Italy and eastern places) at least three subspecies have been found. Ethological analyses show that colony recognition, as indicated by aggressive behavior and the possibilities of adoption in an alien society, is correlated with the composition of cuticular hydrocarbons. Callows can be adopted in an alien colony, they can live in two colonies where the adults do not tolerate each other.
    [Show full text]
  • Hymenoptera: Formicidae)
    ANNALS OF THE UPPER SILESIAN MUSEUM IN BYTOM ENTOMOLOGY Vol. 27 (online 008): 1–51 ISSN 0867-1966, eISSN 2544-039X (online) Bytom, 11.12.2018 SEBASTIAN SALATA1 , LECH BOROWIEC2 Taxonomic and faunistic notes on Greek ants (Hymenoptera: Formicidae) http://doi.org/10.5281/zenodo.2199191 1 Institute for Agricultural and Forest Environment, Polish Academy of Sciences, Bukowska 19, 60-809 Poznań, Poland 2 Department of Biodiversity and Evolutionary Taxonomy, University of Wrocław, Przybyszewskiego 65, 51-148 Wrocław, Poland e-mail: 1 [email protected], 2 [email protected] Abstract: Cataglyphis cretica (FOREL, 1910) is raised to species rank and redescribed. The following synonymies are proposed: Lepisiota nigra (DALLA TORRE, 1893) = Lepisiota splendens KARAVAIEV, 1912 syn. nov.; Camponotus boghossiani FOREL, 1911 = Camponotus boghossiani stenoticus EMERY, 1915 syn. nov.; Camponotus oertzeni FOREL, 1889 = Camponotus andrius DALLA TORRE, 1893 syn. nov., = Campnotus oertzeni kappariensis DALLA TORRE, 1893 syn. nov. Gynes of Aphaenogaster aktaci KIRAN & TEZCAN, 2008, Temnothorax angustifrons Csősz, Heinze & Mikó, 2015, Temnothorax dessyi (MENOZZI, 1936), Temnothorax kemali (SANTSCHI, 1934), Temnothorax smyrnensis (FOREL, 1911) and Temnothorax solerii (MENOZZI, 1936) are described for the first time. Aphaenogaster aktaci KIRAN & TEZCAN, 2008 and Temnothorax kemali (SANTSCHI, 1934) are new to Europe and Greece. New records for 10 species and an updated checklist of 315 species or morphospecies occurring in Greece is given. Key words: redescription, new status, species new to Europe, species new to Greece, ants, Greece. INTRODUCTION Ant fauna of Greece has been intensively studied in recent years. The first impulse for studies on Greek ant fauna was the publication of a checklist by LEGAKIS (2011).
    [Show full text]