Classification of the Bees Or the Superfamily Apoidea
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Wild Bees of Grand Staircase-Escalante National Monument: Richness, Abundance, and Spatio-Temporal Beta-Diversity
Wild bees of Grand Staircase-Escalante National Monument: richness, abundance, and spatio-temporal beta-diversity Olivia Messinger Carril1, Terry Griswold2, James Haefner3 and Joseph S. Wilson4 1 Santa Fe, NM, United States of America 2 USDA-ARS Pollinating Insects Research Unit, Logan, UT, United States of America 3 Biology Department, Emeritus Professor, Utah State University, Logan, UT, United States of America 4 Department of Biology, Utah State University - Tooele, Tooele, UT, United States of America ABSTRACT Interest in bees has grown dramatically in recent years in light of several studies that have reported widespread declines in bees and other pollinators. Investigating declines in wild bees can be difficult, however, due to the lack of faunal surveys that provide baseline data of bee richness and diversity. Protected lands such as national monuments and national parks can provide unique opportunities to learn about and monitor bee populations dynamics in a natural setting because the opportunity for large-scale changes to the landscape are reduced compared to unprotected lands. Here we report on a 4-year study of bees in Grand Staircase-Escalante National Monument (GSENM), found in southern Utah, USA. Using opportunistic collecting and a series of standardized plots, we collected bees throughout the six-month flowering season for four consecutive years. In total, 660 bee species are now known from the area, across 55 genera, and including 49 new species. Two genera not previously known to occur in the state of Utah were discovered, as well as 16 new species records for the state. Bees include ground-nesters, cavity- and twig-nesters, cleptoparasites, narrow specialists, generalists, solitary, and social species. -
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, -
Apoidea (Insecta: Hymenoptera). Fauna of New Zealand 57, 295 Pp. Donovan, B. J. 2007
Donovan, B. J. 2007: Apoidea (Insecta: Hymenoptera). Fauna of New Zealand 57, 295 pp. EDITORIAL BOARD REPRESENTATIVES OF L ANDCARE R ESEARCH Dr D. Choquenot Landcare Research Private Bag 92170, Auckland, New Zealand Dr R. J. B. Hoare Landcare Research Private Bag 92170, Auckland, New Zealand REPRESENTATIVE OF UNIVERSITIES Dr R.M. Emberson c/- Bio-Protection and Ecology Division P.O. Box 84, Lincoln University, New Zealand REPRESENTATIVE OF M USEUMS Mr R.L. Palma Natural Environment Department Museum of New Zealand Te Papa Tongarewa P.O. Box 467, Wellington, New Zealand REPRESENTATIVE OF OVERSEAS I NSTITUTIONS Dr M. J. Fletcher Director of the Collections NSW Agricultural Scientific Collections Unit Forest Road, Orange NSW 2800, Australia * * * SERIES EDITOR Dr T. K. Crosby Landcare Research Private Bag 92170, Auckland, New Zealand Fauna of New Zealand Ko te Aitanga Pepeke o Aotearoa Number / Nama 57 Apoidea (Insecta: Hymenoptera) B. J. Donovan Donovan Scientific Insect Research, Canterbury Agriculture and Science Centre, Lincoln, New Zealand [email protected] Manaaki W h e n u a P R E S S Lincoln, Canterbury, New Zealand 2007 4 Donovan (2007): Apoidea (Insecta: Hymenoptera) Copyright © Landcare Research New Zealand Ltd 2007 No part of this work covered by copyright may be reproduced or copied in any form or by any means (graphic, electronic, or mechanical, including photocopying, recording, taping information retrieval systems, or otherwise) without the written permission of the publisher. Cataloguing in publication Donovan, B. J. (Barry James), 1941– Apoidea (Insecta: Hymenoptera) / B. J. Donovan – Lincoln, N.Z. : Manaaki Whenua Press, Landcare Research, 2007. (Fauna of New Zealand, ISSN 0111–5383 ; no. -
Hymenoptera (Stinging Wasps)
Return to insect order home Page 1 of 3 Visit us on the Web: www.gardeninghelp.org Insect Order ID: Hymenoptera (Stinging Wasps) Life Cycle–Complete metamorphosis: Queens or solitary adults lay eggs. Larvae eat, grow and molt. This stage is repeated a varying number of times, depending on species, until hormonal changes cause the larvae to pupate. Inside a cell (in nests) or a pupal case (solitary), they change in form and color and develop wings. The adults look completely different from the larvae. Solitary wasps: Social wasps: Adults–Stinging wasps have hard bodies and most have membranous wings (some are wingless). The forewing is larger than the hindwing and the two are hooked together as are all Hymenoptera, hence the name "married wings," but this is difficult to see. Some species fold their wings lengthwise, making their wings look long and narrow. The head is oblong and clearly separated from the thorax, and the eyes are compound eyes, but not multifaceted. All have a cinched-in waist (wasp waist). Eggs are laid from the base of the ovipositor, while the ovipositor itself, in most species, has evolved into a stinger. Thus only females have stingers. (Click images to enlarge or orange text for more information.) Oblong head Compound eyes Folded wings but not multifaceted appear Cinched in waist long & narrow Return to insect order home Page 2 of 3 Eggs–Colonies of social wasps have at least one queen that lays both fertilized and unfertilized eggs. Most are fertilized and all fertilized eggs are female. Most of these become workers; a few become queens. -
Seasonal and Spatial Patterns of Mortality and Sex Ratio in the Alfalfa
Seasonal and spatial patterns of mortality and sex ratio in the alfalfa leafcutting bee, Megachile rotundata (F.) by Ruth Pettinga ONeil A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in Entomology Montana State University © Copyright by Ruth Pettinga ONeil (2004) Abstract: Nests from five seed alfalfa sites of the alfalfa leafcutting bee Megachile rotundata (F.) were monitored over the duration of the nesting season in 2000 and 2001, from early July through late August. Cells containing progeny of known age and known position within the nest were subsequently analyzed for five commonly encountered categories of pre-diapause mortality in this species. Chalkbrood and pollen ball had the strongest seasonal relationships of mortality factors studied. Chalkbrood incidence was highest in early-produced cells. Pollen ball was higher in late-season cells. Chalkbrood, parasitism by the chalcid Pteromalus venustus, and death of older larvae and prepupae , due to unknown source(s) exhibited the strongest cell-position relationships. Both chalkbrood and parasitoid incidence were highest in the inner portions of nests. The “unknown” category of mortality was highest in outer portions of nests. Sex ratio was determined for a subset of progeny reared to adulthood. The ratio of females to males is highest in cells in inner nest positions. Sex ratio is female-biased very early in the nesting season, when all cells being provisioned are the inner cells of nests, due to the strong positional effect on sex ratio. SEASONAL AND SPATIAL PATTERNS OF MORTALITY AND SEX RATIO IN THE ALFALFA LEAFCUTTING BEE, Megachile rotundata (F.) by . -
Solanaceae) Flower–Visitor Network in an Atlantic Forest Fragment in Southern Brazil
diversity Article Bee Diversity and Solanum didymum (Solanaceae) Flower–Visitor Network in an Atlantic Forest Fragment in Southern Brazil Francieli Lando 1 ID , Priscila R. Lustosa 1, Cyntia F. P. da Luz 2 ID and Maria Luisa T. Buschini 1,* 1 Programa de Pós Graduação em Biologia Evolutiva da Universidade Estadual do Centro-Oeste, Rua Simeão Camargo Varela de Sá 03, Vila Carli, Guarapuava 85040-080, Brazil; [email protected] (F.L.); [email protected] (P.R.L.) 2 Research Centre of Vascular Plants, Palinology Research Centre, Botanical Institute of Sao Paulo Government, Av. Miguel Stéfano, 3687 Água Funda, São Paulo 04045-972, Brazil; [email protected] * Correspondence: [email protected] Received: 9 November 2017; Accepted: 8 January 2018; Published: 11 January 2018 Abstract: Brazil’s Atlantic Forest biome is currently undergoing forest loss due to repeated episodes of devastation. In this biome, bees perform the most frequent pollination system. Over the last decade, network analysis has been extensively applied to the study of plant–pollinator interactions, as it provides a consistent view of the structure of plant–pollinator interactions. The aim of this study was to use palynological studies to obtain an understanding of the relationship between floral visitor bees and the pioneer plant S. didymum in a fragment of the Atlantic Forest, and also learn about the other plants that interact to form this network. Five hundred bees were collected from 32 species distributed into five families: Andrenidae, Apidae, Colletidae, Megachilidae, and Halictidae. The interaction network consisted of 21 bee species and 35 pollen types. -
Food Load Manipulation Ability Shapes Flight Morphology in Females Of
Polidori et al. Frontiers in Zoology 2013, 10:36 http://www.frontiersinzoology.com/content/10/1/36 RESEARCH Open Access Food load manipulation ability shapes flight morphology in females of central-place foraging Hymenoptera Carlo Polidori1*, Angelica Crottini2, Lidia Della Venezia3,5, Jesús Selfa4, Nicola Saino5 and Diego Rubolini5 Abstract Background: Ecological constraints related to foraging are expected to affect the evolution of morphological traits relevant to food capture, manipulation and transport. Females of central-place foraging Hymenoptera vary in their food load manipulation ability. Bees and social wasps modulate the amount of food taken per foraging trip (in terms of e.g. number of pollen grains or parts of prey), while solitary wasps carry exclusively entire prey items. We hypothesized that the foraging constraints acting on females of the latter species, imposed by the upper limit to the load size they are able to transport in flight, should promote the evolution of a greater load-lifting capacity and manoeuvrability, specifically in terms of greater flight muscle to body mass ratio and lower wing loading. Results: Our comparative study of 28 species confirms that, accounting for shared ancestry, female flight muscle ratio was significantly higher and wing loading lower in species taking entire prey compared to those that are able to modulate load size. Body mass had no effect on flight muscle ratio, though it strongly and negatively co-varied with wing loading. Across species, flight muscle ratio and wing loading were negatively correlated, suggesting coevolution of these traits. Conclusions: Natural selection has led to the coevolution of resource load manipulation ability and morphological traits affecting flying ability with additional loads in females of central-place foraging Hymenoptera. -
Redalyc.CLEPTOPARASITE BEES, with EMPHASIS on THE
Acta Biológica Colombiana ISSN: 0120-548X [email protected] Universidad Nacional de Colombia Sede Bogotá Colombia ALVES-DOS-SANTOS, ISABEL CLEPTOPARASITE BEES, WITH EMPHASIS ON THE OILBEES HOSTS Acta Biológica Colombiana, vol. 14, núm. 2, 2009, pp. 107-113 Universidad Nacional de Colombia Sede Bogotá Bogotá, Colombia Available in: http://www.redalyc.org/articulo.oa?id=319027883009 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Acta biol. Colomb., Vol. 14 No. 2, 2009 107 - 114 CLEPTOPARASITE BEES, WITH EMPHASIS ON THE OILBEES HOSTS Abejas cleptoparásitas, con énfasis en las abejas hospederas coletoras de aceite ISABEL ALVES-DOS-SANTOS1, Ph. D. 1Departamento de Ecologia, IBUSP. Universidade de São Paulo, Rua do Matão 321, trav 14. São Paulo 05508-900 Brazil. [email protected] Presentado 1 de noviembre de 2008, aceptado 1 de febrero de 2009, correcciones 7 de julio de 2009. ABSTRACT Cleptoparasite bees lay their eggs inside nests constructed by other bee species and the larvae feed on pollen provided by the host, in this case, solitary bees. The cleptoparasite (adult and larvae) show many morphological and behavior adaptations to this life style. In this paper I present some data on the cleptoparasite bees whose hosts are bees specialized to collect floral oil. Key words: solitary bee, interspecific interaction, parasitic strategies, hospicidal larvae. RESUMEN Las abejas Cleptoparásitas depositan sus huevos en nidos construídos por otras especies de abejas y las larvas se alimentan del polen que proveen las hospederas, en este caso, abejas solitarias. -
Hymenoptera: Crabronidae)
Paleontological Contributions Number 10I A new genus and species of pemphredonine wasp in Late Cretaceous Vendean amber (Hymenoptera: Crabronidae) Daniel J. Bennett, Vincent Perrichot, and Michael S. Engel December 1, 2014 Lawrence, Kansas, USA ISSN 1946-0279 (online) paleo.ku.edu/contributions Paleontological Contributions December 1, 2014 Number 10I A NEW GENUS AND SPECIES OF PEMPHREDONINE WASP IN LATE CRETACEOUS VENDEAN AMBER (HYMENOPTERA: CRABRONIDAE) Daniel J. Bennett1, Vincent Perrichot2,3,*, and Michael S. Engel3,4 1Department of Biology, Stephen F. Austin State University, P.O. Box 13003, SFA Station, Nacogdoches, Texas, 75962-3003, USA, ben- [email protected], 2CNRS UMR 6118 Géosciences & Observatoire des Sciences de l’Univers de Rennes, Université Rennes 1, 263 avenue du Général Leclerc, 35042 Rennes, France, [email protected], 3University of Kansas Biodiversity Institute, Division of Entomology (Paleoentomology), and 4Department of Ecology & Evolutionary Biology, University of Kansas, 1501 Crestline Drive – Suite 140, Lawrence, Kansas 66045, USA, [email protected] ABSTRACT A new genus and species of pemphredonine wasp is described and figured in Late Cretaceous (Cenomanian to Santonian) amber from Vendée, in northwestern France. Menopsila dupeae n. gen. and sp., is based on a partial male preserved in a small sliver of translucent amber. The genus is placed incertae sedis within the Pemphredonini, as it intermingles features, likely plesiomorphies, of various lineages within the tribe. It likely represents a stem group to one or more of the constituent subtribes, yet it is arguably most similar to the Spilomenina. Keywords: Insecta, Apoidea, Spheciformes, Pemphredoninae, Cretaceous, France RÉSUMÉ Un nouveau genre et une nouvelle espèce de guêpe pemphredonine sont décrits de l’ambre crétacé supérieur (Cénomanien à Santonien) de Vendée, nord-ouest de la France. -
Bees of Sub-Saharan Africa Poster
Bees of Sub-Saharan Africa It is estimated that there are around 30 000 bee species worldwide of which about 20 500 have been described, 2755 occur in sub-Saharan Africa and about 1200 occur in South Africa. Bees, in many shapes and sizes, pollinate about 80% of all flowering plants and 75% of the vegetables, fruits and nuts we eat. The symbols next to each bee indicate their sociality, where they nest and where they get their food. Megachilidae are long tongued bees with two submarginal cells on their wings that collect pollen Apidae are long tongued bees with two or three submarginal wing cells that collect pollen on their hind legs. under their abdomens. The group comprises almost every type of nest building behaviour. Most are solitary but some are social. Parasitism includes social parasites, cleptoparasites and robbers. ♂ ♂ ♀ ♀ ♀ ♀ ♀ ♂ C ♀ C ♀ ♂ F Pasites ♀ appletoni C C F Cleft Cuckoo Ammobates ♀ Nomada gigas Bee auster Gnathanthidium Wasp Cuckoo Sandwalker prionognathum Bee Cuckoo Bee F Big Jawed Afromelecta fulvohirta Euaspis abdominalis Xylocopa lugubris Fidelia braunsiana Redtailed Cuckoo Bee Carder Bee Coelioxys circumscriptus Large Carpenter Bee Pathwork Cuckoo Bee Pot Bee Cone Cuckoo Bee ♀ ♂ ♀ ♀ ♂ C ♂ ♀ F ♂ C ♂ ♀ ♀ ♂ ♀ ♀ F ♀ ♂ F Ceratina Sphecodopsis Icteranthidium ♀ ♂ Schwarzia emmae moerenhouti Max Cuckoo Bee vespericena F grohmani Small Carpenter Bee Cape Cuckoo Ridge Cheeked Bee C F Hoplitis similis Carder Bee F Lithurgus spiniferus Big Resin Bee Aglaoapis trifasciata Stone Bee Toothed Cuckoo Bee F ♀ ♂ ♀ ♂ Aspidosmia arnoldi ♀ ♂ Ugly Faced Carder Bee ♀ F ♀ ♀ Thyreus pictus Xylocopa scioensis F F Neon Cuckoo Bee Afroheriades sp. ♀ Large Carpenter Bee Compsomelissa Macrogalea candida African Resin Bee Ochreriades F ♀ Stenoheriades sp. -
Efectos De La Fragmentación Del Hábitat Sobre Himenópteros Antófilos (Insecta) En El Bosque Chaqueño Serrano
Universidad Nacional de Córdoba Facultad de Ciencias Exactas Físicas y Naturales Doctorado en Ciencias Biológicas Manuscrito de Tesis para optar al título de Dra. en Ciencias Biológicas Efectos de la fragmentación del hábitat sobre himenópteros antófilos (Insecta) en el Bosque Chaqueño Serrano Doctorando: Bióloga Mariana Laura Musicante Directora: Dra. Adriana Salvo Co-Director: Dr. Leonardo Galetto Centro de Investigaciones Entomológicas de Córdoba (CIEC) Instituto Multidisciplinario de Biología Vegetal (IMBIV-CONICET) Córdoba, Argentina 2013 Comisión Asesora Dr. Marcelo Aizen Laboratorio Ecotono-Centro Regional Universitario Bariloche (CRUB), Universidad Nacional del Comahue e Instituto de Investigaciones en Biodiversidad y Medioambiente (INIBIOMA), San Carlos de Bariloche. Departamento de Botánica, Museo Argentino de Ciencias Naturales, Buenos Aires. Dr. Marcelo Cabido Instituto Multidisciplinario de Biología Vegetal-CONICT. Universidad Nacional de Córdoba. Dra. Adriana Salvo Centro de Investigaciones Entomológicas de Córdoba. Instituto Multidisciplinario de Biología Vegetal-CONICT Universidad Nacional de Córdoba. Defensa Oral y Pública Lugar y fecha: Calificación: Tribunal ______________________________ _____________________________________ Firma Aclaración ______________________________ _____________________________________ Firma Aclaración ______________________________ ____________________________________ Firma Aclaración A esos pequeños seres que zumbaban ayer y a los que todavía zumban hoy Efectos de la fragmentación del hábitat -
Novitates PUBLISHED by the AMERICAN MUSEUM of NATURAL HISTORY CENTRAL PARK WEST at 79TH STREET, NEW YORK, N.Y
AMERICAN MUSEUM Novitates PUBLISHED BY THE AMERICAN MUSEUM OF NATURAL HISTORY CENTRAL PARK WEST AT 79TH STREET, NEW YORK, N.Y. 10024 Number 2640, pp. 1-24, figs. 1-36, tables 1-3 January 3, 1978 The Bionomics and Immature Stages of the Cleptoparasitic Bee Genus Protepeolus (Anthophoridae, Nomadinae) JEROME G. ROZEN, JR.,' KATHLEEN R. EICKWORT,2 AND GEORGE C. EICKWORT3 ABSTRACT Protepeolus singularis was found attacking cells numerous biological dissimilarities. The first in- in nests of Diadasia olivacea in southeastern Ari- star Protepeolus attacks and kills the pharate last zona. The following biological information is pre- larval instar of the host before consuming the sented: behavior of adult females while searching provisions, a unique feature for nomadine bees. for host nests; intraspecific interactions of fe- First and last larval instars and the pupa are males at the host nesting site; interactions with described taxonomically and illustrated. Brief host adults; oviposition; and such larval activities comparative descriptions of the other larval in- as crawling, killing the host, feeding, defecation, stars are also given. Larval features attest to the and cocoon spinning. In general, adult female be- common origin of Protepeolus and the other havior corresponds to that of other Nomadinae. Nomadinae. Cladistic analysis using 27 characters Females perch for extended periods near nest of mature larvae of the Nomadinae demonstrates entrances and avoid host females, which attack that Isepeolus is a sister group to all the other parasites when encountered. Females apparently Nomadinae known from larvae, including Pro- learn the locations of host nests and return to tepeolus, and that Protepeolus is a sister group to them frequently.