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Sensory and Cognitive Adaptations to Social Living in Insect Societies Tom Wenseleersa,1 and Jelle S
COMMENTARY COMMENTARY Sensory and cognitive adaptations to social living in insect societies Tom Wenseleersa,1 and Jelle S. van Zwedena A key question in evolutionary biology is to explain the solitarily or form small annual colonies, depending upon causes and consequences of the so-called “major their environment (9). And one species, Lasioglossum transitions in evolution,” which resulted in the pro- marginatum, is even known to form large perennial euso- gressive evolution of cells, organisms, and animal so- cial colonies of over 400 workers (9). By comparing data cieties (1–3). Several studies, for example, have now from over 30 Halictine bees with contrasting levels of aimed to determine which suite of adaptive changes sociality, Wittwer et al. (7) now show that, as expected, occurred following the evolution of sociality in insects social sweat bee species invest more in sensorial machin- (4). In this context, a long-standing hypothesis is that ery linked to chemical communication, as measured by the evolution of the spectacular sociality seen in in- the density of their antennal sensillae, compared with sects, such as ants, bees, or wasps, should have gone species that secondarily reverted back to a solitary life- hand in hand with the evolution of more complex style. In fact, the same pattern even held for the socially chemical communication systems, to allow them to polymorphic species L. albipes if different populations coordinate their complex social behavior (5). Indeed, with contrasting levels of sociality were compared (Fig. whereas solitary insects are known to use pheromone 1, Inset). This finding suggests that the increased reliance signals mainly in the context of mate attraction and on chemical communication that comes with a social species-recognition, social insects use chemical sig- lifestyle indeed selects for fast, matching adaptations in nals in a wide variety of contexts: to communicate their sensory systems. -
Comparative Methods Offer Powerful Insights Into Social Evolution in Bees Sarah Kocher, Robert Paxton
Comparative methods offer powerful insights into social evolution in bees Sarah Kocher, Robert Paxton To cite this version: Sarah Kocher, Robert Paxton. Comparative methods offer powerful insights into social evolution in bees. Apidologie, Springer Verlag, 2014, 45 (3), pp.289-305. 10.1007/s13592-014-0268-3. hal- 01234748 HAL Id: hal-01234748 https://hal.archives-ouvertes.fr/hal-01234748 Submitted on 27 Nov 2015 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 (2014) 45:289–305 Review article * INRA, DIB and Springer-Verlag France, 2014 DOI: 10.1007/s13592-014-0268-3 Comparative methods offer powerful insights into social evolution in bees 1 2 Sarah D. KOCHER , Robert J. PAXTON 1Department of Organismic and Evolutionary Biology, Museum of Comparative Zoology, Harvard University, Cambridge, MA, USA 2Institute for Biology, Martin-Luther-University Halle-Wittenberg, Halle, Germany Received 9 September 2013 – Revised 8 December 2013 – Accepted 2 January 2014 Abstract – Bees are excellent models for studying the evolution of sociality. While most species are solitary, many form social groups. The most complex form of social behavior, eusociality, has arisen independently four times within the bees. -
Molecular Ecology and Social Evolution of the Eastern Carpenter Bee
Molecular ecology and social evolution of the eastern carpenter bee, Xylocopa virginica Jessica L. Vickruck, B.Sc., M.Sc. Department of Biological Sciences Submitted in partial fulfillment of the requirements for the degree of PhD Faculty of Mathematics and Science, Brock University St. Catharines, Ontario © 2017 Abstract Bees are extremely valuable models in both ecology and evolutionary biology. Their link to agriculture and sensitivity to climate change make them an excellent group to examine how anthropogenic disturbance can affect how genes flow through populations. In addition, many bees demonstrate behavioural flexibility, making certain species excellent models with which to study the evolution of social groups. This thesis studies the molecular ecology and social evolution of one such bee, the eastern carpenter bee, Xylocopa virginica. As a generalist native pollinator that nests almost exclusively in milled lumber, anthropogenic disturbance and climate change have the power to drastically alter how genes flow through eastern carpenter bee populations. In addition, X. virginica is facultatively social and is an excellent organism to examine how species evolve from solitary to group living. Across their range of eastern North America, X. virginica appears to be structured into three main subpopulations: a northern group, a western group and a core group. Population genetic analyses suggest that the northern and potentially the western group represent recent range expansions. Climate data also suggest that summer and winter temperatures describe a significant amount of the genetic differentiation seen across their range. Taken together, this suggests that climate warming may have allowed eastern carpenter bees to expand their range northward. Despite nesting predominantly in disturbed areas, eastern carpenter bees have adapted to newly available habitat and appear to be thriving. -
Cambodian Journal of Natural History
Cambodian Journal of Natural History Giant ibis census Patterns of salt lick use Protected area revisions Economic contribution of NTFPs New plants, bees and range extensions June 2016 Vol. 2016 No. 1 Cambodian Journal of Natural History ISSN 2226–969X Editors Email: [email protected] • Dr Neil M. Furey, Chief Editor, Fauna & Flora International, Cambodia. • Dr Jenny C. Daltry, Senior Conservation Biologist, Fauna & Flora International, UK. • Dr Nicholas J. Souter, Mekong Case Study Manager, Conservation International, Cambodia. • Dr Ith Saveng, Project Manager, University Capacity Building Project, Fauna & Flora International, Cambodia. International Editorial Board • Dr Stephen J. Browne, Fauna & Flora International, • Dr Sovanmoly Hul, Muséum National d’Histoire Singapore. Naturelle, Paris, France. • Dr Martin Fisher, Editor of Oryx – The International • Dr Andy L. Maxwell, World Wide Fund for Nature, Journal of Conservation, Cambridge, U.K. Cambodia. • Dr L. Lee Grismer, La Sierra University, California, • Dr Brad Pett itt , Murdoch University, Australia. USA. • Dr Campbell O. Webb, Harvard University Herbaria, • Dr Knud E. Heller, Nykøbing Falster Zoo, Denmark. USA. Other peer reviewers for this volume • Prof. Leonid Averyanov, Komarov Botanical Institute, • Neang Thy, Minstry of Environment, Cambodia. Russia. • Dr Nguyen Quang Truong, Institute of Ecology and • Prof. John Blake, University of Florida, USA. Biological Resources, Vietnam. • Dr Stephan Gale, Kadoorie Farm & Botanic Garden, • Dr Alain Pauly, Royal Belgian Institute of Natural Hong Kong. Sciences, Belgium. • Fredéric Goes, Cambodia Bird News, France. • Dr Colin Pendry, Royal Botanical Garden, Edinburgh, • Dr Hubert Kurzweil, Singapore Botanical Gardens, UK. Singapore. • Dr Stephan Risch, Leverkusen, Germany. • Simon Mahood, Wildlife Conservation Society, • Dr Nophea Sasaki, University of Hyogo, Japan. -
Changing Paradigms in Insect Social Evolution: Insights from Halictine and Allodapine Bees
ANRV297-EN52-07 ARI 18 July 2006 2:13 V I E E W R S I E N C N A D V A Changing Paradigms in Insect Social Evolution: Insights from Halictine and Allodapine Bees Michael P. Schwarz,1 Miriam H. Richards,2 and Bryan N. Danforth3 1School of Biological Sciences, Flinders University, Adelaide S.A. 5001, Australia; email: Michael.Schwarz@flinders.edu.au 2Department of Biological Sciences, Brock University, St. Catharines, ON L2S 3A1, Canada; email: [email protected] 3Department of Entomology, Cornell University, Ithaca, New York 14853; email: [email protected] Annu. Rev. Entomol. 2007. 52:127–50 Key Words The Annual Review of Entomology is online at sex allocation, caste determination, phylogenetics, kin selection ento.annualreviews.org This article’s doi: Abstract 10.1146/annurev.ento.51.110104.150950 Until the 1980s theories of social insect evolution drew strongly Copyright c 2007 by Annual Reviews. on halictine and allodapine bees. However, that early work suffered All rights reserved from a lack of sound phylogenetic inference and detailed informa- 0066-4170/07/0107-0127$20.00 tion on social behavior in many critical taxa. Recent studies have changed our understanding of these bee groups in profound ways. It has become apparent that forms of social organization, caste de- termination, and sex allocation are more labile and complex than previously thought, although the terminologies for describing them are still inadequate. Furthermore, the unexpected complexity means that many key parameters in kin selection and reproductive skew models remain unquantified, and addressing this lack of informa- tion will be formidable. -
Wasps and Bees in Southern Africa
SANBI Biodiversity Series 24 Wasps and bees in southern Africa by Sarah K. Gess and Friedrich W. Gess Department of Entomology, Albany Museum and Rhodes University, Grahamstown Pretoria 2014 SANBI Biodiversity Series The South African National Biodiversity Institute (SANBI) was established on 1 Sep- tember 2004 through the signing into force of the National Environmental Manage- ment: Biodiversity Act (NEMBA) No. 10 of 2004 by President Thabo Mbeki. The Act expands the mandate of the former National Botanical Institute to include respon- sibilities relating to the full diversity of South Africa’s fauna and flora, and builds on the internationally respected programmes in conservation, research, education and visitor services developed by the National Botanical Institute and its predecessors over the past century. The vision of SANBI: Biodiversity richness for all South Africans. SANBI’s mission is to champion the exploration, conservation, sustainable use, appreciation and enjoyment of South Africa’s exceptionally rich biodiversity for all people. SANBI Biodiversity Series publishes occasional reports on projects, technologies, workshops, symposia and other activities initiated by, or executed in partnership with SANBI. Technical editing: Alicia Grobler Design & layout: Sandra Turck Cover design: Sandra Turck How to cite this publication: GESS, S.K. & GESS, F.W. 2014. Wasps and bees in southern Africa. SANBI Biodi- versity Series 24. South African National Biodiversity Institute, Pretoria. ISBN: 978-1-919976-73-0 Manuscript submitted 2011 Copyright © 2014 by South African National Biodiversity Institute (SANBI) All rights reserved. No part of this book may be reproduced in any form without written per- mission of the copyright owners. The views and opinions expressed do not necessarily reflect those of SANBI. -
The Biology and External Morphology of Bees
3?00( The Biology and External Morphology of Bees With a Synopsis of the Genera of Northwestern America Agricultural Experiment Station v" Oregon State University V Corvallis Northwestern America as interpreted for laxonomic synopses. AUTHORS: W. P. Stephen is a professor of entomology at Oregon State University, Corval- lis; and G. E. Bohart and P. F. Torchio are United States Department of Agriculture entomolo- gists stationed at Utah State University, Logan. ACKNOWLEDGMENTS: The research on which this bulletin is based was supported in part by National Science Foundation Grants Nos. 3835 and 3657. Since this publication is largely a review and synthesis of published information, the authors are indebted primarily to a host of sci- entists who have recorded their observations of bees. In most cases, they are credited with specific observations and interpretations. However, information deemed to be common knowledge is pre- sented without reference as to source. For a number of items of unpublished information, the generosity of several co-workers is ac- knowledged. They include Jerome G. Rozen, Jr., Charles Osgood, Glenn Hackwell, Elbert Jay- cox, Siavosh Tirgari, and Gordon Hobbs. The authors are also grateful to Dr. Leland Chandler and Dr. Jerome G. Rozen, Jr., for reviewing the manuscript and for many helpful suggestions. Most of the drawings were prepared by Mrs. Thelwyn Koontz. The sources of many of the fig- ures are given at the end of the Literature Cited section on page 130. The cover drawing is by Virginia Taylor. The Biology and External Morphology of Bees ^ Published by the Agricultural Experiment Station and printed by the Department of Printing, Ore- gon State University, Corvallis, Oregon, 1969. -
Molecular Phylogenetics of Allodapine Bees, with Implications for the Evolution of Sociality and Progressive Rearing
Syst. Biol. 52(1):1–14, 2003 DOI: 10.1080/10635150390132632 Molecular Phylogenetics of Allodapine Bees, with Implications for the Evolution of Sociality and Progressive Rearing MICHAEL P. S CHWARZ,1 NICHOLAS J. BULL,1 AND STEVEN J. B. COOPER2 1School of Biological Sciences, Flinders University, G.P.O. Box 2100, Adelaide, South Australia 5001, Australia 2Evolutionary Biology Unit, South Australian Museum, Adelaide, South Australia 5000, Australia Abstract.—Allodapine bees have long been regarded as providing useful material for examining the origins of social behavior. Previous researchers have assumed that sociality arose within the Allodapini and have linked the evolution of sociality to a transition from mass provisioning to progressive provisioning of brood. Early phylogenetic studies of allodapines were based on morphological and life-history data, but critical aspects of these studies relied on small character sets, where the polarity and coding of characters is problematic. We used nucleotide sequence data from one nuclear and two mitochondrial gene fragments to examine phylogenetic structure among nine allodapine genera. Our data set comprised Downloaded from https://academic.oup.com/sysbio/article/52/1/1/1656919 by guest on 03 October 2021 1,506 nucleotide positions, of which 402 were parsimony informative. Maximum parsimony,log determinant, and maximum likelihood analyses produced highly similar phylogenetic topologies, and all analyses indicated that the tropical African genus Macrogalea was the sister group to all other allodapines. This finding conflicts with that of previous studies, in which Compsomelissa + Halterapis formed the most basal group. Changing the basal node of the Allodapini has major consequences for understanding evolution in this tribe. -
Social Complexity in Bees Is Not Sufficient to Explain Lack of Reversions to Solitary Living Over Long Time Scales, BMC Evolutionary Biology, 2007; 7:246
PUBLISHED VERSION Chenoweth, Luke B.; Tierney, Simon Martin; Smith, Jaclyn Ann; Cooper, Steven John Baynard; Schwarz, Michael Peter. Social complexity in bees is not sufficient to explain lack of reversions to solitary living over long time scales, BMC Evolutionary Biology, 2007; 7:246. © 2007 Chenoweth et al; licensee BioMed Central Ltd. PERMISSIONS http://www.biomedcentral.com/info/about/license This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. BioMed Central Open Access license agreement Brief summary of the agreement: Anyone is free: to copy, distribute, and display the work; to make derivative works; to make commercial use of the work; Under the following conditions: Attribution the original author must be given credit; for any reuse or distribution, it must be made clear to others what the license terms of this work are; any of these conditions can be waived if the authors gives permission. nd 2 May 2011 http://hdl.handle.net/2440/60321 BMC Evolutionary Biology BioMed Central Research article Open Access Social complexity in bees is not sufficient to explain lack of reversions to solitary living over long time scales Luke B Chenoweth*†1, Simon M Tierney†2, Jaclyn A Smith1, Steven JB Cooper3 and Michael P Schwarz†1 Address: 1Biological Sciences, Flinders University GPO BOX 2100, Adelaide, SA 5001, Australia, 2Smithsonian Tropical Research Institute, Apartado Postal 0843-03092, Panama, Republica de Panama and 3Evolutionary Biology Unit, South Australian Museum, North Terrace, Adelaide, S.A. -
(Xylocopa) Violacea (L., 1758) (Hymenoptera: Apidae): Female Nest-Defence
Ann. Mus. civ. Rovereto Sez.: Arch., St., Sc. nat. Vol. 12 (1996) 85-100 1998 SALVATORE VICIDOMINI BIOLOGY OF XYLOCOPA (XYLOCOPA) VIOLACEA (L., 1758) (HYMENOPTERA: APIDAE): FEMALE NEST-DEFENCE ALVATORE ICIDOMINI Abstract - S V - Biology of Xylocopa (Xylocopa) violacea (L., 1758) (Hymenoptera: Apidae): female nest defence. X. violacea was observed for 1200 h in 9 years in Southern Italy. Experiment was carried out in order to study the nest defence ethology. The females used for the experiments were the following: 60 females with nest (F); 30 females without nest (*F); 45 18h-imagine-females. The nest defence was exhibited versus following causes: conspecifics, insect intruders, man. Man evoke a particular and unique defence behaviour. The presence of experimenter do not influence the intimidatory buzzing. (F) and (*F) exhibited a buzzing behaviour with a frequency very similar. Repeated tasks do not decrease the buzzing behaviour. Temperature is not important in buzzing exhibition but influences the intensity and the behaviour duration; a exhibited cloudy phase appear more important to decrease buzzing behaviour. Buzzing is innate. Intimidatory buzzing was also observed in: X. fenestrata, combusta, flavorufa, imitator, torrida, pubescens, sulcatipes and in Lestis bombylans e L. aeratus. In X. violacea was not observed the rectal ejection of yellow liquid, observed in: X. combusta, fenestrata, flavorufa, imitator, torrida, ciliata, virginica, Lestis bombylans. The metasomal notum occlusion of nest entrance was frequently observed and also reported in: X. appendiculata, augusti, auripennis, ciliata, tranquebarorum, virginica, combusta, flavorufa, imitator, torrida, pubescens, sulcatipes, Lestis bombylans, L. aeratus. Results shows that acoustic stimuli are very important. Buzzing behaviours are used in intraspecific and interspecific (other insect orders) interactions; for this reason the acoustie sense appear very important in aggressive interactions. -
Phylogenetics of Allodapine Bees: a Review of Social Evolution, Parasitism and Biogeography Simon M
Phylogenetics of allodapine bees: a review of social evolution, parasitism and biogeography Simon M. Tierney, Jaclyn A. Smith, Luke Chenoweth, Michael P. Schwarz To cite this version: Simon M. Tierney, Jaclyn A. Smith, Luke Chenoweth, Michael P. Schwarz. Phylogenetics of allodapine bees: a review of social evolution, parasitism and biogeography. Apidologie, Springer Verlag, 2008, 39 (1), pp.3-15. hal-00891934 HAL Id: hal-00891934 https://hal.archives-ouvertes.fr/hal-00891934 Submitted on 1 Jan 2008 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 39 (2008) 3–15 Available online at: c INRA/DIB-AGIB/ EDP Sciences, 2008 www.apidologie.org DOI: 10.1051/apido:2007045 Review article Phylogenetics of allodapine bees: a review of social evolution, parasitism and biogeography* Simon M. Tierney1,2, Jaclyn A. Smith1,LukeChenoweth1,MichaelP.Schwarz1 1 School of Biological Sciences, Flinders University, GPO Box 2100, Adelaide, S.A. 5001, Australia 2 Smithsonian Tropical Research Institute, Apartado Postal 0843-03092, Balboa, Republic of Panama Received 15 November 2006 – Revised 3 October 2007 – Accepted 3 October 2007 Abstract – It has been assumed that allodapine bees represent early stages in the evolution of social be- haviour. -
A Review of the Xylocopa Species (Hymenoptera: Apidae) of Israel
ISRAEL JOURNAL OF ENTOMOLOGY, Vol. 41–42, 2011–2012, pp. 145–163 A review of the Xylocopa species (Hymenoptera: Apidae) of Israel MOSHE GUERSHON AND ARMIN IONESCU-HIRSCH Department of Zoology, The George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel. E-mail: [email protected] ABSTRACT In this paper we list ten Xylocopa species from Israel, X. fenestrata, X. iris, X. olivieri, X. pubescens, X. rufa, X. sulcatipes, X. ustulata, X. valga, X. va- rentzowi and X. violacea. The distribution in Israel of the newly recorded spe- cies X. ustulata, a widespread, mainly African species that reaches its northern distribution limit in southern Israel, and X. varentzowi, an Irano–Turanian spe- cies that reaches its western distribution limit in northern Israel, is published for the first time. We provide a key for the ten Israeli species, and in order to prevent further confusion, we include also the Afrotropical X. hottentotta, since various Ctenoxylocopa from western Asia, including Israel, were often misidentified with this species in faunistic reports. In addition, information is given on the species’ geographical distribution, worldwide and in Israel, as reported in the literature and recorded in the National Collections of Natural History at Tel Aviv University (TAUI). KEYWORDS: Xylocopa, list, key, distribution, Israel INTRODUCTION The subfamily Xylocopinae (Hymenoptera: Apidae) includes bees that are superficially very varied: the large and robust (13 to 33 mm long) Xylocopini as opposed to the small and slender (3 to 13 mm) Allodapini, Ceratinini and Manueliini (Michener, 2007). In this paper, which deals with the Israeli Xylocopini (Xylocopa Latreille 1802: subgenera Copoxyla Maa, Ctenoxylocopa Michener, Koptortosoma Gribodo, Proxylocopa Hurd and Moure and Xylocopa Lepeletier), we follow the higher classification of Minckley (1998) and Michener (2007).