Hymenoptera: Apidae, Meliponini)
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Classification of the Apidae (Hymenoptera)
Utah State University DigitalCommons@USU Mi Bee Lab 9-21-1990 Classification of the Apidae (Hymenoptera) Charles D. Michener University of Kansas Follow this and additional works at: https://digitalcommons.usu.edu/bee_lab_mi Part of the Entomology Commons Recommended Citation Michener, Charles D., "Classification of the Apidae (Hymenoptera)" (1990). Mi. Paper 153. https://digitalcommons.usu.edu/bee_lab_mi/153 This Article is brought to you for free and open access by the Bee Lab at DigitalCommons@USU. It has been accepted for inclusion in Mi by an authorized administrator of DigitalCommons@USU. For more information, please contact [email protected]. 4 WWvyvlrWryrXvW-WvWrW^^ I • • •_ ••^«_«).•>.• •.*.« THE UNIVERSITY OF KANSAS SCIENC5;^ULLETIN LIBRARY Vol. 54, No. 4, pp. 75-164 Sept. 21,1990 OCT 23 1990 HARVARD Classification of the Apidae^ (Hymenoptera) BY Charles D. Michener'^ Appendix: Trigona genalis Friese, a Hitherto Unplaced New Guinea Species BY Charles D. Michener and Shoichi F. Sakagami'^ CONTENTS Abstract 76 Introduction 76 Terminology and Materials 77 Analysis of Relationships among Apid Subfamilies 79 Key to the Subfamilies of Apidae 84 Subfamily Meliponinae 84 Description, 84; Larva, 85; Nest, 85; Social Behavior, 85; Distribution, 85 Relationships among Meliponine Genera 85 History, 85; Analysis, 86; Biogeography, 96; Behavior, 97; Labial palpi, 99; Wing venation, 99; Male genitalia, 102; Poison glands, 103; Chromosome numbers, 103; Convergence, 104; Classificatory questions, 104 Fossil Meliponinae 105 Meliponorytes, -
Cameroon: Nest Architecture, Behaviour and Labour Calendar
Institut für Nutzpflanzenwissenschaften und Ressourcenschutz Rheinische Friedrich-Wilhelms-Universität Bonn Diversity of Stingless Bees in Bamenda Afromontane Forests – Cameroon: Nest architecture, Behaviour and Labour calendar Dissertation zur Erlangung des Grades Doktor der Agrarwissenschaften (Dr. Agr.) der Hohen Landwirtschaftlichen Fakultät der Rheinischen Friedrich-Wilhelms-Universität zu Bonn vorgelegt am 04. November 2009 von Moses Tita Mogho Njoya aus Lobe Estate, Kamerun Referent: Prof. Dr. D. Wittmann Korreferent: Prof. Dr. A. Skowronek Tag der mündlichen Prüfung: 22. Dezember 2009 Diese Dissertation ist auf dem Hochschulschriftenserver der ULB Bonn http://hss.ulb.uni-bonn.de/diss_online elektronisch publiziert Erscheinungsjahr: 2010 Dedication To my parent who are of blessed memory: Chui George Ntobukeu NJOYA and Tohjeuh Elizabeth Bah. ABSTRACT Until now almost nothing was known of invertebrates such as wild bees in the Bamenda highland forest region in Cameroon. This study focuses on honey producing bee species which do not possess functional stings. The diversity of the stingless bees in this area as well as their nest biology and behaviour was studied. In all, Six species of stingless bees grouped into four genera exist in the Bamenda afro-montane forests. The four genera are: Meliponula (3 species), Dactylurina (1species), Hypotrigona (1 species) and Liotrigona (1species). The most represented of the species in Bamenda was Liotrigona. Stingless bees were found to have huge variations in habitat preferences and in nest architectures. Nest designs differ with species as well as the habitats. Nest were found in tree trunks, mud walls, traditional hives, in soils or even just attached to tree branches. Brood cells and storage pots differ from species to species. -
Nestmate Recognition in the Stingless Bee Frieseomelitta Varia (Hymenoptera, Apidae, Meliponini): Sources of Chemical Signals
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Animal Behaviour 81 (2011) 463e467 Contents lists available at ScienceDirect Animal Behaviour journal homepage: www.elsevier.com/locate/anbehav Nestmate recognition in the stingless bee Frieseomelitta varia (Hymenoptera, Apidae, Meliponini): sources of chemical signals Túlio M. Nunes a,*, Sidnei Mateus a, Izabel C. Turatti b, E. David Morgan c, Ronaldo Zucchi a a Departamento de Biologia, Faculdade de Filosofia Ciências e Letras de Ribeirão Preto, Universidade de São Paulo b Departamento de Física e Química, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo c Chemical Ecology Group, Lennard-Jones Laboratory, Keele University article info Social insects use cuticular lipids for nestmate recognition. These lipids are chiefly hydrocarbons that can Article history: be endogenously produced or acquired from the environment. Although these compounds are already Received 14 April 2010 described as coming from different sources for different groups of social insects, nothing is known about Initial acceptance 31 May 2010 the source of cuticular hydrocarbons in stingless bees. We used behavioural recognition tests and cuticle Final acceptance 15 November 2010 chemical investigation to elucidate the role of endogenous and environmentally based cues for nestmate Available online 24 December 2010 recognition in the stingless bee Frieseomelitta varia. We found that although newly emerged workers MS. number: A10-00258R present specific cuticle patterns according to their nest origin, these compounds are not used for nest- mate recognition, since newly emerged workers are broadly accepted in different colonies. The cerumen Keywords: used in nest construction played an important role in recognition behaviour. -
Stingless Bee Nesting Biology David W
Stingless bee nesting biology David W. Roubik To cite this version: David W. Roubik. Stingless bee nesting biology. Apidologie, Springer Verlag, 2006, 37 (2), pp.124-143. hal-00892207 HAL Id: hal-00892207 https://hal.archives-ouvertes.fr/hal-00892207 Submitted on 1 Jan 2006 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Apidologie 37 (2006) 124–143 124 c INRA/DIB-AGIB/ EDP Sciences, 2006 DOI: 10.1051/apido:2006026 Review article Stingless bee nesting biology* David W. Ra,b a Smithsonian Tropical Research Institute, Apartado 0843-03092, Balboa, Ancón, Panamá, República de Panamá b Unit 0948, APO AA 34002-0948, USA Received 2 October 2005 – Revised 29 November 2005 – Accepted 23 December 2005 Abstract – Stingless bees diverged since the Cretaceous, have 50 times more species than Apis,andare both distinctive and diverse. Nesting is capitulated by 30 variables but most do not define clades. Both architectural features and behavior decrease vulnerability, and large genera vary in nest habit, architecture and defense. Natural stingless bee colony density is 15 to 1500 km−2. Symbionts include mycophagic mites, collembolans, leiodid beetles, mutualist coccids, molds, and ricinuleid arachnids. -
Warfare in Stingless Bees
Insect. Soc. (2016) 63:223–236 DOI 10.1007/s00040-016-0468-0 Insectes Sociaux REVIEW ARTICLE Warfare in stingless bees 1,2 1,3 4 5 C. Gru¨ter • L. G. von Zuben • F. H. I. D. Segers • J. P. Cunningham Received: 24 August 2015 / Revised: 28 January 2016 / Accepted: 6 February 2016 / Published online: 29 February 2016 Ó International Union for the Study of Social Insects (IUSSI) 2016 Abstract Bees are well known for being industrious pol- how victim colonies are selected, but a phylogenetically linators. Some species, however, have taken to invading the controlled analysis suggests that the notorious robber bee nests of other colonies to steal food, nest material or the nest Lestrimelitta preferentially attacks colonies of species with site itself. Despite the potential mortality costs due to more concentrated honey. Warfare among bees poses many fighting with an aggressive opponent, the prospects of a interesting questions, including why species differ so large bounty can be worth the risk. In this review, we aim to greatly in their response to attacks and how these alternative bring together current knowledge on intercolony fighting strategies of obtaining food or new nest sites have evolved. with a view to better understand the evolution of warfare in bees and identify avenues for future research. A review of Keywords Stingless bees Á Warfare Á literature reveals that at least 60 species of stingless bees are Alternative foraging strategies Á Cleptoparasitism Á involved in heterospecific conflicts, either as attacking or Lestrimelitta Á Meliponini victim colonies. The threat of invasion has led to the evo- lution of architectural, behavioural and morphological adaptations, such as narrow entrance tunnels, mud balls to Introduction block the entrance, decoy nests that direct invaders away from the brood chamber, fighting swarms, and soldiers that The nest is the all-important centre of the bee’s universe, are skilled at immobilising attackers. -
Duckeola) Ghilianii (With 3 Text-Figures and 2 Tables
Title Oviposition behavior of an Amazonic Stingless Bee, Trigona (Duckeola) ghilianii (With 3 Text-figures and 2 Tables) Author(s) SAKAGAMI, Shôichi F.; ZUCCHI, Ronaldo Citation 北海道大學理學部紀要, 16(4), 564-581 Issue Date 1968-12 Doc URL http://hdl.handle.net/2115/27466 Type bulletin (article) File Information 16(4)_P564-581.pdf Instructions for use Hokkaido University Collection of Scholarly and Academic Papers : HUSCAP Oviposition behavior of an Amazonic Stingless Bee, Trigona (Duckeola) ghilianie)2) By Shoichi F. Sakagami and Ronaldo Zucchi Zoological Institute, Hokkaido University, Sapporo, Japan and Departamento de Genetica, Faculdade de Filosofia, Ci€mcias e Letras de Ribeirao Preto, Brasil (With 3 Text-figures and 2 Table.s) As the seventh report of our serial work on the oviposition behavior of the stingless bees, the present paper deals with Trigona (Duckeola) ghilianii Spinola, 1853, an aberrant species representing a monospecific offshoot within the Trigona Tetragona Oomplex. An enormous nest of this species was discovered and taken at Ponta Negra near Manaus, Amazonas, on January 28, 1963, by the members of the Faculdade de Filosofia, Oiencias e Letras de Rio Olaro Expedition to Amazonas. The colony was transported by air to Rio Claro, State of Sao Paulo, and introduced on Feburary 15, into an observation hive of the type used in our previous work (Sakagami, 1966). The colony lost a considerable part of the original population in the course of extraction and transport, but the remaining inhabitants well adapted themselves to the artificial conditions. The first oviposition was observed on February 19 and the observations described below were made intermittently until June 30, 1963. -
Atlas of Pollen and Plants Used by Bees
AtlasAtlas ofof pollenpollen andand plantsplants usedused byby beesbees Cláudia Inês da Silva Jefferson Nunes Radaeski Mariana Victorino Nicolosi Arena Soraia Girardi Bauermann (organizadores) Atlas of pollen and plants used by bees Cláudia Inês da Silva Jefferson Nunes Radaeski Mariana Victorino Nicolosi Arena Soraia Girardi Bauermann (orgs.) Atlas of pollen and plants used by bees 1st Edition Rio Claro-SP 2020 'DGRV,QWHUQDFLRQDLVGH&DWDORJD©¥RQD3XEOLFD©¥R &,3 /XPRV$VVHVVRULD(GLWRULDO %LEOLRWHF£ULD3ULVFLOD3HQD0DFKDGR&5% $$WODVRISROOHQDQGSODQWVXVHGE\EHHV>UHFXUVR HOHWU¶QLFR@RUJV&O£XGLD,Q¬VGD6LOYD>HW DO@——HG——5LR&ODUR&,6(22 'DGRVHOHWU¶QLFRV SGI ,QFOXLELEOLRJUDILD ,6%12 3DOLQRORJLD&DW£ORJRV$EHOKDV3µOHQ– 0RUIRORJLD(FRORJLD,6LOYD&O£XGLD,Q¬VGD,, 5DGDHVNL-HIIHUVRQ1XQHV,,,$UHQD0DULDQD9LFWRULQR 1LFRORVL,9%DXHUPDQQ6RUDLD*LUDUGL9&RQVXOWRULD ,QWHOLJHQWHHP6HUYL©RV(FRVVLVWHPLFRV &,6( 9,7¯WXOR &'' Las comunidades vegetales son componentes principales de los ecosistemas terrestres de las cuales dependen numerosos grupos de organismos para su supervi- vencia. Entre ellos, las abejas constituyen un eslabón esencial en la polinización de angiospermas que durante millones de años desarrollaron estrategias cada vez más específicas para atraerlas. De esta forma se establece una relación muy fuerte entre am- bos, planta-polinizador, y cuanto mayor es la especialización, tal como sucede en un gran número de especies de orquídeas y cactáceas entre otros grupos, ésta se torna más vulnerable ante cambios ambientales naturales o producidos por el hombre. De esta forma, el estudio de este tipo de interacciones resulta cada vez más importante en vista del incremento de áreas perturbadas o modificadas de manera antrópica en las cuales la fauna y flora queda expuesta a adaptarse a las nuevas condiciones o desaparecer. -
Insect Egg Size and Shape Evolve with Ecology but Not Developmental Rate Samuel H
ARTICLE https://doi.org/10.1038/s41586-019-1302-4 Insect egg size and shape evolve with ecology but not developmental rate Samuel H. Church1,4*, Seth Donoughe1,3,4, Bruno A. S. de Medeiros1 & Cassandra G. Extavour1,2* Over the course of evolution, organism size has diversified markedly. Changes in size are thought to have occurred because of developmental, morphological and/or ecological pressures. To perform phylogenetic tests of the potential effects of these pressures, here we generated a dataset of more than ten thousand descriptions of insect eggs, and combined these with genetic and life-history datasets. We show that, across eight orders of magnitude of variation in egg volume, the relationship between size and shape itself evolves, such that previously predicted global patterns of scaling do not adequately explain the diversity in egg shapes. We show that egg size is not correlated with developmental rate and that, for many insects, egg size is not correlated with adult body size. Instead, we find that the evolution of parasitoidism and aquatic oviposition help to explain the diversification in the size and shape of insect eggs. Our study suggests that where eggs are laid, rather than universal allometric constants, underlies the evolution of insect egg size and shape. Size is a fundamental factor in many biological processes. The size of an 526 families and every currently described extant hexapod order24 organism may affect interactions both with other organisms and with (Fig. 1a and Supplementary Fig. 1). We combined this dataset with the environment1,2, it scales with features of morphology and physi- backbone hexapod phylogenies25,26 that we enriched to include taxa ology3, and larger animals often have higher fitness4. -
Genes Involved in Convergent Evolution of Eusociality in Bees
Genes involved in convergent evolution of eusociality in bees S. Hollis Woodarda,1, Brielle J. Fischmana,1, Aarti Venkatb, Matt E. Hudsonb, Kranthi Varalab, Sydney A. Cameronc, Andrew G. Clarkd, and Gene E. Robinsona,c,e,f,2 aProgram in Ecology, Evolution, and Conservation Biology, Departments of bCrop Sciences and cEntomology, eInstitute for Genomic Biology, and fNeuroscience Program, University of Illinois, Urbana, IL 61801; and dDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853 Contributed by Gene E. Robinson, March 12, 2011 (sent for review February 17, 2011) Eusociality has arisen independently at least 11 times in insects. different social lifestyles among relatively closely related species. Despite this convergence, there are striking differences among Furthermore, the extensive knowledge of bee natural history (8, eusocial lifestyles, ranging from species living in small colonies 13, 14) provides a valuable framework for developing hypotheses with overt conflict over reproduction to species in which colonies about the adaptive significance of genetic changes detected in contain hundreds of thousands of highly specialized sterile work- eusocial bee lineages. ers produced by one or a few queens. Although the evolution of To study patterns of molecular evolution associated with eusociality has been intensively studied, the genetic changes eusociality in bees, we generated ~1 Gbp of expressed sequence involved in the evolution of eusociality are relatively unknown. tags (ESTs) from a set of nine bee species (Table S1). This set of We examined patterns of molecular evolution across three in- species reflects the remarkable social diversity in bees by in- dependent origins of eusociality by sequencing transcriptomes of cluding eusocial and non-eusocial species; three origins of euso- nine socially diverse bee species and combining these data with ciality (9, 10); and two different forms of eusocial lifestyle, “highly genome sequence from the honey bee Apis mellifera to generate eusocial” and “primitively eusocial” (ref. -
WORLD LIST of EDIBLE INSECTS 2015 (Yde Jongema) WAGENINGEN UNIVERSITY PAGE 1
WORLD LIST OF EDIBLE INSECTS 2015 (Yde Jongema) WAGENINGEN UNIVERSITY PAGE 1 Genus Species Family Order Common names Faunar Distribution & References Remarks life Epeira syn nigra Vinson Nephilidae Araneae Afregion Madagascar (Decary, 1937) Nephilia inaurata stages (Walck.) Nephila inaurata (Walckenaer) Nephilidae Araneae Afr Madagascar (Decary, 1937) Epeira nigra Vinson syn Nephila madagscariensis Vinson Nephilidae Araneae Afr Madagascar (Decary, 1937) Araneae gen. Araneae Afr South Africa Gambia (Bodenheimer 1951) Bostrichidae gen. Bostrichidae Col Afr Congo (DeFoliart 2002) larva Chrysobothris fatalis Harold Buprestidae Col jewel beetle Afr Angola (DeFoliart 2002) larva Lampetis wellmani (Kerremans) Buprestidae Col jewel beetle Afr Angola (DeFoliart 2002) syn Psiloptera larva wellmani Lampetis sp. Buprestidae Col jewel beetle Afr Togo (Tchibozo 2015) as Psiloptera in Tchibozo but this is Neotropical Psiloptera syn wellmani Kerremans Buprestidae Col jewel beetle Afr Angola (DeFoliart 2002) Psiloptera is larva Neotropicalsee Lampetis wellmani (Kerremans) Steraspis amplipennis (Fahr.) Buprestidae Col jewel beetle Afr Angola (DeFoliart 2002) larva Sternocera castanea (Olivier) Buprestidae Col jewel beetle Afr Benin (Riggi et al 2013) Burkina Faso (Tchinbozo 2015) Sternocera feldspathica White Buprestidae Col jewel beetle Afr Angola (DeFoliart 2002) adult Sternocera funebris Boheman syn Buprestidae Col jewel beetle Afr Zimbabwe (Chavanduka, 1976; Gelfand, 1971) see S. orissa adult Sternocera interrupta (Olivier) Buprestidae Col jewel beetle Afr Benin (Riggi et al 2013) Cameroun (Seignobos et al., 1996) Burkina Faso (Tchimbozo 2015) Sternocera orissa Buquet Buprestidae Col jewel beetle Afr Botswana (Nonaka, 1996), South Africa (Bodenheimer, 1951; syn S. funebris adult Quin, 1959), Zimbabwe (Chavanduka, 1976; Gelfand, 1971; Dube et al 2013) Scarites sp. Carabidae Col ground beetle Afr Angola (Bergier, 1941), Madagascar (Decary, 1937) larva Acanthophorus confinis Laporte de Cast. -
Brown and Oliveira Apidologie
1 The impact of agricultural colonization and deforestation on stingless bee (Apidae: 2 Meliponini) composition and richness in Rondônia, Brazil 3 4 J. Christopher BROWN1, Marcio Luiz de OLIVEIRA2 5 6 1 Department of Geography, University of Kansas, 1475 Jayhawk Blvd., 223, Lawrence, 7 KS 66045, USA. [email protected] 8 2 Coordenação de Pesquisas em Biodiversidade, Instituto Nacional de Pesquisas da 9 Amazônia, Av. André Araújo 2936, Caixa postal 2223, Manaus, AM 69060-971, Brazil. 10 [email protected] 11 12 Short title: Deforestation and stingless bees 13 14 Abstract 15 Stingless bees were collected throughout the state of Rondônia in the southwestern 16 Brazilian Amazon for one year. The impact of agricultural colonization and subsequent 17 deforestation on species composition and richness is explored. Deforestation, around each 18 of 187 sample sites, was characterized at meso, micro, and local spatial scales. At the 19 micro-scale, deforestation was measured using a data layer generated by satellite remote 20 sensing and analyzed with the assistance of a geographic information system. We report 21 perhaps the greatest richness of stingless bees ever recorded in the tropics, collecting 22 9,555 individuals from 98 species of stingless bees. Ten of these are new species and 16 23 were first-ever records for Rondônia. Five new species were scientifically described from 1 24 the study. We report statistical relationships between deforestation and species richness at 25 all spatial scales of analysis, and we tentatively identify species that appear to be 26 especially sensitive to deforestation. 27 28 Key-words: social bees; redundancy analysis; forest fragmentation; land use; 29 Amazon 30 2 31 1. -
Secretions of Stingless Bees: the Dufour Glands of Some Frieseomelitta Species (Apidae, Meliponinae) Eda Flávia L.R.A
Secretions of stingless bees: the Dufour glands of some Frieseomelitta species (Apidae, Meliponinae) Eda Flávia L.R.A. Patricio, Leopoldo López, Roland Maile, E. David Morgan To cite this version: Eda Flávia L.R.A. Patricio, Leopoldo López, Roland Maile, E. David Morgan. Secretions of stingless bees: the Dufour glands of some Frieseomelitta species (Apidae, Meliponinae). Apidologie, Springer Verlag, 2003, 34 (4), pp.359-365. 10.1051/apido:2003027. hal-00891787 HAL Id: hal-00891787 https://hal.archives-ouvertes.fr/hal-00891787 Submitted on 1 Jan 2003 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Apidologie 34 (2003) 359–365 © INRA/DIB-AGIB/ EDP Sciences, 2003 359 DOI: 10.1051/apido:2003027 Original article Secretions of stingless bees: the Dufour glands of some Frieseomelitta species (Apidae, Meliponinae) Eda Flávia L.R.A. PATRICIOa, Leopoldo CRUZ LÓPEZb,c, Roland MAILEb, E. David MORGANb* a Laboratório de Abelhas, Instituto de Biociências, Universidade de Saõ Paulo, 05508-900 Saõ Paulo SP, Brasil b Chemical Ecology Group, Lennard-Jones Laboratory, School of Chemistry and Physics, Keele University, Staffs., ST5 5BG, UK c Present address: El Colegio de la Frontera Sur, Carretera Antiguo Aeropuerto Km.