Guide to the Wood Ants of the UK

Total Page:16

File Type:pdf, Size:1020Kb

Guide to the Wood Ants of the UK Guide to the Wood Ants of the UK and related species © Stewart Taylor © Stewart Taylor Wood Ants of the UK This guide is aimed at anyone who wants to learn more about mound-building woodland ants in the UK and how to identify the three ‘true’ Wood Ant species: Southern Red Wood Ant, Scottish Wood Ant and Hairy Wood Ant. The Blood-red Ant and Narrow-headed Ant (which overlap with the Wood Ants in their appearance, habitat and range) are also included here. The Shining Guest Ant is dependent on Wood Ants for survival so is included in this guide to raise awareness of this tiny and overlooked species. A further related species, Formica pratensis is not included in this guide. It has been considered extinct on mainland Britain since 2005 and is now only found on Jersey and Guernsey in the British Isles. Funding by CLIF, National Parks Protectors Published by the Cairngorms National Park Authority © CNPA 2021. All rights reserved. Contents What are Wood Ants? 02 Why are they important? 04 The Wood Ant calendar 05 Colony establishment and life cycle 06 Scottish Wood Ant 08 Hairy Wood Ant 09 Southern Red Wood Ant 10 Blood-red Ant 11 Narrow-headed Ant 12 Shining Guest Ant 13 Comparison between Shining Guest Ant and Slender Ant 14 Where to find Wood Ants 15 Nest mounds 18 Species distributions 19 Managing habitat for wood ants 22 Survey techniques and monitoring 25 Recording Wood Ants 26 Conservation status of Wood Ants 27 Further information 28 01 What are Wood Ants? Wood Ants are large, red and brown-black ants and in Europe most species live in woodland habitats. They are known around the world as thatch or mound ants due to the mounded nests they build. There are 13 described species of these ants in Eurasia and 19 species in North America. Like all ants they are social and cooperate to look after the brood, care for the nest and source food. Biology and ecology Wood Ants build large thatched dried grass and even pieces of lichen. mounds in which to live and The thatch acts like a solar panel aggressively defend both their nest to raise the temperature of the and food resources. As their name nest above that of its surroundings suggests, they are associated with (a high temperature is crucial for woodland; coniferous forest, mixed brood development). The thatch and broadleaf woodland with well also acts as an umbrella so that rain drained soils being favoured. Nests water trickles away from the nest, are usually south or south-east facing keeping it dry. to maximise the amount of sunlight warming the nest. All species of ants in the UK hibernate over the winter. In Nest mounds vary tremendously mound-building ants, they retreat in size and shape, ranging from fist- to the underground parts of their sized to 2m tall. What you see above nests where the temperature is ground is at least mirrored (and stable and free of frost. The best sometimes exceeded) underground. time to look for active nests is Internally the nest contains a series from spring to autumn. Ants of tunnels and chambers containing emerge from hibernation once the queen, a nursery for the brood temperatures are consistently and food stores. Tunnel entrances above freezing and ‘swarm’ on the can be opened or closed to maintain surface of the nest in sunny weather optimal temperature and humidity. to warm themselves (and boost the temperature of the nest). The On the surface, the ‘thatch’ is made movement of the ants swarming of organic materials such as pine on the nest surface in spring needles, small twigs, moss, heather, actually makes an audible sound. 02 Swarming behaviour of Wood Ant workers on the nest surface in spring. Queens rise to the surface at this time and can be identified by their larger size in relation to the workers and their large glossy abdomens. © Jenni Stockan © Jenni Diet Wood Ants are omnivorous and prey on a wide range of other invertebrates. Caterpillars, aphids, spiders, beetles and many others (including other ants) are taken, their diet changing to suit local abundances of different prey. Workers subdue their prey by biting and spraying formic acid. A small proportion of © J.M.S.Robinson their diet includes seeds, tree sap and berry juices. They will also scavenge A Southern Wood Ant on dead invertebrates. (Formica rufa) worker guarding a collection of aphids. Between 60% and 90% of the diet of the workers comes from honeydew produced by aphids feeding on the sap of trees and shrubs. This sap is high in sugars and as the aphids feed they excrete excess sugars as honeydew. Ants ‘milk’ the aphids of Ants ‘milk’ the aphids of their honeydew, and in return protect their honeydew, and in the aphids from predators and even “ ” return protect the aphids move them to better feeding grounds. The Blood-red Ant is predominantly from predators and even predatory on other ants but will move them to better also feed on seeds, berries and take feeding grounds. honeydew from aphids. 03 Why are they important? Not only are Wood Ants fascinating and beautiful insects in their own right, but they perform a number of important roles in the forest ecosystem, earning them the status of “ecosystem engineers”. Wood Ants: The Wood Ant’s nest is home to a unique community of specialist • Affect tree growth through their invertebrates. This includes the relationship with aphids in the Shining Guest Ant but also specially tree canopy and through removal adapted beetles, moths and even of insect herbivores (e.g. moth woodlice which live inside ant caterpillars) mounds and nowhere else. There • Accumulate huge amounts of is also a concentration of micro- organic material and minerals in organisms within Wood Ant nests their nests, particularly nitrogen which breakdown unwanted food and phosphorus (the nests not and nest materials. only increase the amount of mineral nutrients but also make them more available to plants) • Help distribute the seeds of plants, including some plant species which have sugary coatings on their seeds to make them attractive to ants • Are used by a range of bird species to remove parasites (behaviour known as ‘anting’ – birds aggregate the surface of the nest, causing the ants to © Wiswell Hayley spray formic acid onto the bird’s feathers which kills parasites) Larva of the beetle Clytra quadripunctata with its case In addition Wood Ants are a food made of plant material. The source for vertebrates such as larvae wander about on the Capercaillie, Badger and Pine Marten surface of Wood Ant nests to name a few. Some species feeding on plant debris and specialise in feeding on Wood Ants, use their case as protection such as the Green Woodpecker from the Wood Ant workers. and the Gallows Spider. 04 The Wood Ant calendar This is generalised across the species in this guide and timing of events will vary between species and parts of the UK, nest altitude, local climate etc. November – February/March June – September Hibernation Raising worker offspring March – April May – June Spring swarming (Wood Ants only, Raising queens and males timing dependent on ambient (from eggs laid in late winter/ temperature and levels of sunshine). early spring). In southern UK, Wood Ants can emerge as early as February, depending on weather. Activity of the workers begins when the internal nest temperature rises to between 25-30°C. May – October June – August General worker activity – foraging, Emergence of virgin queens and aphid farming, repairing and building males, mating flights take place. nest. Number of active workers This is usually confined to a involved in foraging peaks in mid- relatively short window of 2-3 summer. Size of individual workers weeks. In southern England can varies greatly within the colony be as early as May, in northern and depends on the quality of diet Scotland may be as late as during the larval stage. July-August 05 Colony establishment and life cycle 1 Mating Queens and males undertake mating flights. Queens drop their wings soon after mating. 2 Colony establishment Social parasitism Mated queen Nest budding Establishes a new colony returns to natal nest takes place by parasitising the nest of When there are a different ant species multiple queens in a single nest 3 Lifecycle of an ant Queen Queen lays eggs Male Hatch into larvae Pupate when fully Worker developed – pupae can be cocooned or ‘naked’. 06 1.1 Mating Wood Ants and Narrow-headed Ants can Colony establishment and life cycle exist in ‘super colonies’ which comprise Newly emerged queens and males take of multiple mounds (known as polydomy, to the wing. Males usually emerge first which means ‘many homes’). Workers and disperse to reduce chances of mating moving in between them to exchange with queens from their own nests. Takes resources. Nest budding allows a gradual place in the morning on still, warm days. dispersal through a habitat, and allows the colony to be adaptable to changes 2.2 Colony establishment in habitat and food resources. Social parasitism 3 Life cycle of an ant A newly mated queen flies from her natal nest and establishes a new colony Only queens lay eggs. Eggs hatch into by parasitising the nest of a different ant larvae and then undergo complete species – in the UK the host species are metamorphosis to become adult ants. Formica fusca, F. lemani and F. cunicularia. Larvae are fed a protein rich diet (insect The Wood Ant queen enters the nest prey, particularly caterpillars). Workers of the host, kills or excludes the queen move larvae and pupae around the and then uses the host workers to raise nest to the warmest areas to optimise her own offspring.
Recommended publications
  • Killarney, Barraduff & Gneeveguilla Wwtp Discharges Natura Impact Statement
    KERRY COUNTY COUNCIL COMHAIRLE CONTAE CHIARRAÍ KILLARNEY, BARRADUFF & GNEEVEGUILLA WWTP DISCHARGES NATURA IMPACT STATEMENT For inspection purposes only. Consent of copyright owner required for any other use. JANUARY 2010 CONSULTING ENGINEERS Sherwood House, Sherwood Avenue, Taylor’s Hill, Galway Suite D4, The Cubes Offices, Beacon South Quarter, Sandyford Dublin 18 EPA Export 04-11-2011:03:50:18 Quality Control CLIENT Kerry County Council PROJECT NO 2178 PROJECT TITLE KILLARNEY, BARRADUFF & GNEEVEGUILLA WWTP DISCHARGES REPORT TITLE NATURA IMPACT STATEMENT Rev. Status Author(s) Reviewed By Approved By Issue Date 1 ISSUE GH MJ MJ 04.03.2011 For inspection purposes only. Consent of copyright owner required for any other use. Natura Impact Statement Page 2 EPA Export 04-11-2011:03:50:18 TABLE OF CONTENTS 1 INTRODUCTION ............................................................................................ 4 1.1 BACKGROUND.....................................................................................................................4 1.2 APPROPRIATE ASSESSMENT – LEGISLATIVE CONTEXT...............................................5 1.3 NATURA 2000 SITES ...........................................................................................................7 1.4 SCHEME LOCATIONS..........................................................................................................8 2 METHODOLOGY.......................................................................................... 11 2.1 DESK STUDY......................................................................................................................
    [Show full text]
  • A Review of the Ant Genera Leptothorax Mayr and Temnothorax Mayr (Hymenoptera, Formicidae) of the Eastern Palaearctic
    Acta Zoologica Academiae Scientiarum Hungaricae 50 (2), pp. 109–137, 2004 A REVIEW OF THE ANT GENERA LEPTOTHORAX MAYR AND TEMNOTHORAX MAYR (HYMENOPTERA, FORMICIDAE) OF THE EASTERN PALAEARCTIC A. RADCHENKO Museum and Institute of Zoology, Polish Academy of Sciences 64, Wilcza str., 00–679, Warsaw, Poland; E-mail: [email protected] Nineteen species of the genera Leptothorax and Temnothorax are distributed from Mongolia to the Pacific Ocean, these are revised and a key to their identification is provided. Four new species, Temnothorax cuneinodis, T. xanthos, T. pisarskii and T. michali are described from North Korea. L. galeatus WHEELER is synonymised with T. nassonovi (RUZSKY) and L. wui WHEELER is raised to species rank (in the genus Temnothorax). Key words: ants, Leptothorax, Temnothorax, taxonomy, new species, key, East Palaearctic INTRODUCTION The genus Leptothorax was described by MAYR in 1855, and a few years later he described the closely related genus Temnothorax (MAYR, 1861). For many years, the latter was regarded by different authors either as a good genus or as a subgenus of Leptothorax, but during the last decade it was considered to be a junior synonym of Leptothorax (BOLTON, 1995). BINGHAM (1903) designated Formica acervorum FABRICIUS, 1793 as the type-species of the genus Leptothorax. About the same time RUZSKY (1904) de- scribed the genus Mychothorax, to which F. acervorum was also assigned as type species (by original designation); later Mychothorax was considered as a subgenus of Leptothorax, insomuch that EMERY (1912, 1921) designated Myrmica clypeata MAYR, 1853 as the type species of Leptothorax. All subsequent authors placed the species with 11-jointed antennae in the subgenus Mychothorax and those with 12-jointed antennae in the subgenus Leptothorax s.
    [Show full text]
  • A Taxonomic Revision of the Palaearctic Members of the Formica Rufa Group (Hymeno­Ptera: Formicidae) – the Famous Mound-Building Red Wood Ants Bernhard Seifert
    ISSN 1997-3500 Myrmecological News myrmecologicalnews.org Myrmecol. News 31: 133-179 doi: 10.25849/myrmecol.news_031:133 28 April 2021 Original Article ZooBank LSID: 0E55C0D7-531A-48D7-A078-148B96BD461D A taxonomic revision of the Palaearctic members of the Formica rufa group (Hymeno ptera: Formicidae) – the famous mound-building red wood ants Bernhard Seifert Abstract A revision of the Palaearctic members of the Formica rufa group, the famous mound-building red wood ants, is pre- sented based on Numeric Morphology-Based Alpha-Taxonomy (NUMOBAT) and on genetic information from studies published in cooperation with others. Standardized morphological character systems were described numerically to allow objective hypothesis formation by exploratory data analyses and testing by hypothesis-driven data analyses. NU- MOBAT data were recorded in a total of 1200 samples with 5500 worker individuals and 410 gynes. Comparative tables to workers and gynes of all species and the most frequent hybrids and a key to the workers are presented. Considering 54 available names, the survey recognized 13 good species, 32 junior synonyms and eight names not interpretable to species level (incertae sedis). The ratio of junior synonyms against the number of recognized species is elevenfold the ratio found in a revision of Palaearctic Lasius s.str. conducted by the same author in 2020 with basically the same methodology. Excessive name production in the F. rufa group is partly result of the big attention these eye-catching ants have received by naturalists but it also reflects the enormous difficulties to reasonably interpret a multitude of phenotypes. These difficulties are caused by extraordinary frequency of reticulate evolution, particular mechanisms for the evolution of deviating local populations, and intraspecific polymorphism with differences sometimes being larger than those between species.
    [Show full text]
  • 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.
    [Show full text]
  • Somerset's Ecological Network
    Somerset’s Ecological Network Mapping the components of the ecological network in Somerset 2015 Report This report was produced by Michele Bowe, Eleanor Higginson, Jake Chant and Michelle Osbourn of Somerset Wildlife Trust, and Larry Burrows of Somerset County Council, with the support of Dr Kevin Watts of Forest Research. The BEETLE least-cost network model used to produce Somerset’s Ecological Network was developed by Forest Research (Watts et al, 2010). GIS data and mapping was produced with the support of Somerset Environmental Records Centre and First Ecology Somerset Wildlife Trust 34 Wellington Road Taunton TA1 5AW 01823 652 400 Email: [email protected] somersetwildlife.org Front Cover: Broadleaved woodland ecological network in East Mendip Contents 1. Introduction .................................................................................................................... 1 2. Policy and Legislative Background to Ecological Networks ............................................ 3 Introduction ............................................................................................................... 3 Government White Paper on the Natural Environment .............................................. 3 National Planning Policy Framework ......................................................................... 3 The Habitats and Birds Directives ............................................................................. 4 The Conservation of Habitats and Species Regulations 2010 ..................................
    [Show full text]
  • 409-456 Rejstriky Olomoucko1
    Bibliografie 1. ALBRECHT, P. (1996–2000): Inventarizaãní prÛzkumy 19. BEZDùâKA, P. (1983): Lesní mravenci na lokalitû Alf- âubernice, Lipovské upolínové louky, Na HÛrkách, rédka. – Na‰í pfiírodou, 2: 18–19, Praha. Pod Pansk˘m lesem, Vitãick˘ les, Za Hrnãífikou. – 20. BEZDùâKA, P. (1998): Mravenci Pfiírodního parku Vel- Depon. in RÎP OkÚ Prostûjov, 25 s., 38 s., 17 s., 15 k˘ Kosífi. – Pfiírodovûdné studie Muzea Prostûjovska, s., 32 s., 25 s., Prostûjov. (nepubl.) 1: 125–132, Prostûjov. 2. ALBRECHT, P. (1998): Krajiny Prostûjovska. – Pfiírodo- 21. BEZDùâKA, P. (1999): V˘voj komplexu hnízd Formica vûdné studie Muzea Prostûjovska, 1: 47–66, Prostûjov. lugubris Zett. v Jeseníkách. – Formica, zpravodaj pro 3. ALBRECHT, P. (1999): Fytocenologické snímky moni- aplikovan˘ v˘zkum a ochranu lesních mravencÛ, 2: torovacích ploch LIPO 02.01 a 02.02. Správa CHKO 65–70, Liberec. Litovelské Pomoraví, 3 s., Olomouc. (nepubl.) 22. BUâEK, A. (1979): Pfiíspûvek k inventarizaci SPR Bu- 4. ALBRECHT, P. (2000): Pfiíspûvek ke kvûtenû nejvy‰‰ích koveãek. MS, práce SOâ pfii SLT· Hranice, 18 s., ãástí Drahanské vrchoviny se zamûfiením na mokfiady. Hranice. – Pfiírodovûdné studie Muzea Prostûjovska, 3: 55–86, 23. BURE·, L., BURE·OVÁ, Z. (1988): âerven˘ seznam cév- Prostûjov. nat˘ch rostlin CHKO Jeseníky. – Zpravodaj âSOP, 3: 5. ANDùRA, M. (1999): âeské názvy ÏivoãichÛ II. Savci 1–28, Bruntál. (Mammalia). Národní muzeum, 148 s., Praha. 24. BURE·, L., BURE·OVÁ, Z. (1989): Velká kotlina, státní 6. ANDùRA, M., HANZAL, V. (1996): Atlas roz‰ífiení sav- pfiírodní rezervace. – PrÛvodce nauãnou stezkou, cÛ v âeské republice. PfiedbûÏná verze. II: ·elmy (Car- âSOP ZO, 44 s., Ostrava. nivora).
    [Show full text]
  • Download PDF File (107KB)
    Myrmecological News 15 Digital supplementary material Digital supplementary material to SEPPÄ, P., HELANTERÄ, H., TRONTTI, K., PUNTTILA, P., CHERNENKO, A., MARTIN, S.J. & SUNDSTRÖM, L. 2011: The many ways to delimit species: hairs, genes and surface chemistry. – Myrmecological News 15: 31-41. Appendix 1: Number of hairs on different body parts of Formica fusca and F. lemani according to different authors. Promesonotum & pronotum YARROW COLLINGWOOD DLUSSKY & KUTTER COLLINGWOOD DOUWES CZECHOWSKI & SEIFERT SEIFERT (1954) (1958) PISARSKI (1971) (1977) (1979) (1995) al. (2002) (1996) (2007) F. fusca < 3 at most 2 - 3 ≤ 2 usually 0, usually = 0, ≤ 2 usually 0, rarely average average sometimes occasion. 1 - 2 1 - 5 < 1 0 - 0.8 1 - 4 F. lemani numerous numerous some ind. >10, up to 20 "with erect ≥ 3 > 6 average average in SE-Europ. popu- hairs" > 1 1.2 - 13.5 lations, most ind. 0 Femora F. fusca mid = 0 mid = 0 mid = 0 mid ≤ 1 fore = 2 - 3 hind = 0 hind = 0 mid = rarely 1 - 2 F. lemani mid = "long all = "hairy" mid = a few mid ≥ 2 fore = 3 - 12 hairs" hind = a few mid = 3 - 17 References COLLINGWOOD, C.A. 1958: A key to the species of ants (Hymenoptera, Formicidae) found in Britain. – Transactions of the Society for British Entomology 13: 69-96. COLLINGWOOD, C.A. 1979: The Formicidae (Hymenoptera) of Fennoscandia and Denmark. – Fauna Entomologica Scandinavica 8: 1-174. CZECHOWSKI, W., RADCHENKO, A. & CZECHOWSKA, W. 2002: The ants (Hymenoptera, Formicidae) of Poland. – Museum and Insti- tute of Zoology PAS, Warszawa, 200 pp. DLUSSKY, G.M. & PISARSKI, B. 1971: Rewizja polskich gatunków mrówek (Hymenoptera: Formicidae) z rodzaju Formica L.
    [Show full text]
  • Akes an Ant an Ant? Are Insects, and Insects Are Arth Ropods: Invertebrates (Animals With­
    ~ . r. workers will begin to produce eggs if the queen dies. Because ~ eggs are unfertilized, they usually develop into males (see the discus­ : ~ iaplodiploidy and the evolution of eusociality later in this chapter). =- cases, however, workers can produce new queens either from un­ ze eggs (parthenogenetically) or after mating with a male ant. -;c. ant colony will continue to grow in size and add workers, but at -: :;oint it becomes mature and will begin sexual reproduction by pro· . ~ -irgin queens and males. Many specie s produce males and repro­ 0 _ " females just before the nuptial flight . Others produce males and ---: : ._ tive fem ales that stay in the nest for a long time before the nuptial :- ~. Our largest carpenter ant, Camponotus herculeanus, produces males _ . -:= 'n queens in late summer. They are groomed and fed by workers :;' 0 it the fall and winter before they emerge from the colonies for their ;;. ights in the spring. Fin ally, some species, including Monomoriurn : .:5 and Myrmica rubra, have large colonies with multiple que ens that .~ ..ew colonies asexually by fragmenting the original colony. However, _ --' e polygynous (literally, many queens) and polydomous (literally, uses, referring to their many nests) ants eventually go through a -">O=- r' sexual reproduction in which males and new queens are produced. ~ :- . ant colony thus functions as a highly social, organ ized "super­ _ _ " 1." The queens and mo st workers are safely hidden below ground : : ~ - ed within the interstices of rotting wood. But for the ant workers ~ '_i S ' go out and forage for food for the colony,'life above ground is - =- .
    [Show full text]
  • Origins and Affinities of the Ant Fauna of Madagascar
    Biogéographie de Madagascar, 1996: 457-465 ORIGINS AND AFFINITIES OF THE ANT FAUNA OF MADAGASCAR Brian L. FISHER Department of Entomology University of California Davis, CA 95616, U.S.A. e-mail: [email protected] ABSTRACT.- Fifty-two ant genera have been recorded from the Malagasy region, of which 48 are estimated to be indigenous. Four of these genera are endemic to Madagascar and 1 to Mauritius. In Madagascar alone,41 out of 45 recorded genera are estimated to be indigenous. Currently, there are 318 names of described species-group taxa from Madagascar and 381 names for the Malagasy region. The ant fauna of Madagascar, however,is one of the least understoodof al1 biogeographic regions: 2/3of the ant species may be undescribed. Associated with Madagascar's long isolation from other land masses, the level of endemism is high at the species level, greaterthan 90%. The level of diversity of ant genera on the island is comparable to that of other biogeographic regions.On the basis of generic and species level comparisons,the Malagasy fauna shows greater affinities to Africathan to India and the Oriental region. Thestriking gaps in the taxonomic composition of the fauna of Madagascar are evaluatedin the context of island radiations.The lack of driver antsin Madagascar may have spurred the diversification of Cerapachyinae and may have permitted the persistenceof other relic taxa suchas the Amblyoponini. KEY W0RDS.- Formicidae, Biogeography, Madagascar, Systematics, Africa, India RESUME.- Cinquante-deux genres de fourmis, dont 48 considérés comme indigènes, sontCOMUS dans la région Malgache. Quatre d'entr'eux sont endémiques de Madagascaret un seul de l'île Maurice.
    [Show full text]
  • Actes Des Colloques Insectes Sociaux
    U 2 I 0 E 0 I 2 S ACTES DES COLLOQUES INSECTES SOCIAUX Edité par l'Union Internationale pour l’Etude des Insectes Sociaux - Section française (sous la direction de François-Xavier DECHAUME MONCHARMONT et Minh-Hà PHAM-DELEGUE) VOL. 15 (2002) – COMPTE RENDU DU COLLOQUE ANNUEL 50e anniversaire - Versailles - 16-18 septembre 2002 ACTES DES COLLOQUES INSECTES SOCIAUX Edité par l'Union Internationale pour l’Etude des Insectes Sociaux - Section française (sous la direction de François-Xavier DECHAUME MONCHARMONT et Minh-Hà PHAM-DELEGUE) VOL. 15 (2002) – COMPTE RENDU DU COLLOQUE ANNUEL 50e anniversaire - Versailles - 16-18 septembre 2002 ISSN n° 0265-0076 ISBN n° 2-905272-14-7 Composé au Laboratoire de Neurobiologie Comparée des Invertébrés (INRA, Bures-sur-Yvette) Publié on-line sur le site des Insectes Sociaux : : http://www.univ-tours.fr/desco/UIEIS/UIEIS.htm Comité Scientifique : Martin GIURFA Université Toulouse Alain LENOIR Université Tours Christian PEETERS CNRS Paris 6 Minh-Hà PHAM-DELEGUE INRA Bures Comité d'Organisation : Evelyne GENECQUE F.X. DECHAUME MONCHARMONT Et toute l’équipe du LNCI (INRA Bures) Nous remercions sincèrement l’INRA et l’établissement THOMAS qui ont soutenu financièrement cette manifestation. Crédits Photographiques Couverture : 1. Abeille : Serge CARRE (INRA) 2. Fourmis : Photothèque CNRS 3. Termite : Alain ROBERT (Université de Bourgogne, Dijon) UIEIS Versailles Page 1 Programme UNION INTERNATIONALE POUR L’ETUDE DES INSECTES SOCIAUX UIEIS Section Française - 50ème Anniversaire Versailles 16-18 Septembre 2002 PROGRAMME Lundi 16 septembre 9 h ACCUEIL DES PARTICIPANTS - CAFE 10 h Présentation du Centre INRA de Versailles – Président du Centre Session Plasticité et Socialité- Modérateur Martin Giurfa 10 h 15 - Conférence Watching the bee brain when it learns – Randolf Menzel (Université Libre de Berlin) 11 h 15 Calcium responses to queen pheromones, social pheromones and plant odours in the antennal lobe of the honey bee drone Apis mellifera L.
    [Show full text]
  • Ecography E6629 Machac, A., Janda, M., Dunn, R
    Ecography E6629 Machac, A., Janda, M., Dunn, R. R. and Sanders, N. J. 2010. Elevational gradients in phylogenetic structure of ant communities reveal the interplay of biotic and abiotic constraints on species density. – Ecography 33: xxx–xxx. Supplementary material system is 250–2000 m (Fig. S1); we have sampled approximate- ly 90% of the extent of this elevational gradient (Sanders et al. 2007). Vorarlberg Mts (2600 km2) consist of several montane systems Appendix 1 (Silvretta, Ratikon, Verwall, Arlberg) formed during the Alpine orogeny (65 mya) (Fenninger et al. 1980). Flora and fauna of the region have been largely affected during the ice ages. Nowadays, Geography of the montane systems the temperate climate predominates but, indeed, fluctuates with elevation (350–3000 m) (Austrian Geological Survey 2010) (Fig. The geological system of Great Smoky Mts (2000 km2) was formed S1). approximately 200–300 mya. The mountains’ convenient north- Chiricahua Mts (2200 km2), composed of Tertiary volcanics, south orientation allowed the species to migrate along their slopes are situated in the deserts of southeastern Arizona, USA (Jenney during the times of climate changes (e.g. ice age 10 kya) (King and Reynolds 1989). Particular biological diversity of the moun- 1968). Therefore, the environment of Smoky Mts remained un- tain range stems from its position on the interface of four ecological disturbed by climate fluctuations for over a million years, hence, regions (Sonoran desert, Chihuahuan desert, Rocky Mountains, providing species a sufficient time for wide diversifications (US and Sierra Madre) (US Geological Survey 2010). The elevational Geological Survey 2010). The elevational span of the montane gradient spans from 1100 to 2900 m (Fig.
    [Show full text]
  • Review and Phylogenetic Evaluation of Associations Between Microdontinae (Diptera: Syrphidae) and Ants (Hymenoptera: Formicidae)
    Hindawi Publishing Corporation Psyche Volume 2013, Article ID 538316, 9 pages http://dx.doi.org/10.1155/2013/538316 Review Article Review and Phylogenetic Evaluation of Associations between Microdontinae (Diptera: Syrphidae) and Ants (Hymenoptera: Formicidae) Menno Reemer Naturalis Biodiversity Center, European Invertebrate Survey, P.O. Box 9517, 2300 RA Leiden, The Netherlands Correspondence should be addressed to Menno Reemer; [email protected] Received 11 February 2013; Accepted 21 March 2013 Academic Editor: Jean-Paul Lachaud Copyright © 2013 Menno Reemer. 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 immature stages of hoverflies of the subfamily Microdontinae (Diptera: Syrphidae) develop in ant nests, as predators ofthe ant brood. The present paper reviews published and unpublished records of associations of Microdontinae with ants, in order to discuss the following questions. (1) Are all Microdontinae associated with ants? (2) Are Microdontinae associated with all ants? (3) Are particular clades of Microdontinae associated with particular clades of ants? (4) Are Microdontinae associated with other insects? A total number of 109 associations between the groups are evaluated, relating to 43 species of Microdontinae belonging to 14 genera, and to at least 69 species of ants belonging to 24 genera and five subfamilies. The taxa of Microdontinae found in association with ants occur scattered throughout their phylogenetic tree. One of the supposedly most basal taxa (Mixogaster)isassociatedwith ants, suggesting that associations with ants evolved early in the history of the subfamily and have remained a predominant feature of their lifestyle.
    [Show full text]