A Guide to Some Bees and Wasps of Indonesia
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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. -
A New Record of Aulacidae (Hymenoptera: Evanioidea) from Korea
Journal of Asia-Pacific Biodiversity Vol. 6, No. 4 419-422, 2013 http://dx.doi.org/10.7229/jkn.2013.6.4.00419 A New Record of Aulacidae (Hymenoptera: Evanioidea) from Korea Jin-Kyung Choi1, Jong-Chul Jeong2 and Jong-Wook Lee1* 1Department of Life Sciences, Yeungnam University, Gyeongsan, 712-749, Korea 2National Park Research Institute, Korea National Park Service, Namwon, 590-811, Korea Abstract: Pristaulacus comptipennis Enderlein, 1912 is redescribed and illustrated based on a recently collected specimen in Korea. With a newly recorded species, P. comptipennis Enderlein, a total of six Korean aulacids are recognized: Aulacus salicius Sun and Sheng, 2007, Pristaulacus insularis Konishi, 1990, P. intermedius Uchida, 1932, P. kostylevi Alekseyev, 1986, P. jirisani Smith and Tripotin, 2011, and P. comptipennis Enderlein, 1912. A key to species of Korean Aulacidae is provided with, redescription and diagnostic characteristics of Pristaulacus comptipennis. Keywords: Aulacidae, Pristaulacus comptipennis, new record, Korea Introduction of Yeungnam University (YNU, Gyeongsan, Korea). Also, for identification of Korean Aulacidae, type materials of Family Aulacidae currently includes 244 extant species some species were borrowed from NIBR. Images were placed in two genera: Aulacus Jurine, 1807 with 76 species obtained using a stereo microscope (Zeiss Stemi SV 11 and Pristaulacus Kieffer, 1900 with 168 species. Members Apo; Carl Zeiss, Göttingen, Germany). The key characters of this family are distributed in all zoogeographic regions shown in the photographs were produced using a Delta except Antarctica (e.g. Benoit 1984; Lee & Turrisi 2008; imaging system (i-Delta 2.6; iMTechnology, Daejeon, Smith and Tripotin 2011; Turrisi and Smith 2011). The Korea). -
Megachile (Callomegachile) Sculpturalis Smith, 1853 (Apoidea: Megachilidae): a New Exotic Species in the Iberian Peninsula, and Some Notes About Its Biology
Butlletí de la Institució Catalana d’Història Natural, 82: 157-162. 2018 ISSN 2013-3987 (online edition): ISSN: 1133-6889 (print edition)157 GEA, FLORA ET fauna GEA, FLORA ET FAUNA Megachile (Callomegachile) sculpturalis Smith, 1853 (Apoidea: Megachilidae): a new exotic species in the Iberian Peninsula, and some notes about its biology Oscar Aguado1, Carlos Hernández-Castellano2, Emili Bassols3, Marta Miralles4, David Navarro5, Constantí Stefanescu2,6 & Narcís Vicens7 1 Andrena Iniciativas y Estudios Medioambientales. 47007 Valladolid. Spain. 2 CREAF. 08193 Cerdanyola del Vallès. Spain. 3 Parc Natural de la Zona Volcànica de la Garrotxa. 17800 Olot. Spain. 4 Ajuntament de Sant Celoni. Bruc, 26. 08470 Sant Celoni. Spain. 5 Unitat de Botànica. Universitat Autònoma de Barcelona. 08193 Cerdanyola del Vallès. Spain. 6 Museu de Ciències Naturals de Granollers. 08402 Granollers. Spain. 7 Servei de Medi Ambient. Diputació de Girona. 17004 Girona. Spain. Corresponding author: Oscar Aguado. A/e: [email protected] Rebut: 20.09.2018; Acceptat: 26.09.2018; Publicat: 30.09.2018 Abstract The exotic bee Megachile sculpturalis has colonized the European continent in the last decade, including some Mediterranean countries such as France and Italy. In summer 2018 it was recorded for the first time in Spain, from several sites in Catalonia (NE Iberian Peninsula). Here we give details on these first records and provide data on its biology, particularly of nesting and floral resources, mating behaviour and interactions with other species. Key words: Hymenoptera, Megachilidae, Megachile sculpturalis, exotic species, biology, Iberian Peninsula. Resum Megachile (Callomegachile) sculpturalis Smith, 1853 (Apoidea: Megachilidae): una nova espècie exòtica a la península Ibèrica, amb notes sobre la seva biologia L’abella exòtica Megachile sculpturalis ha colonitzat el continent europeu en l’última dècada, incloent alguns països mediterranis com França i Itàlia. -
UFRJ a Paleoentomofauna Brasileira
Anuário do Instituto de Geociências - UFRJ www.anuario.igeo.ufrj.br A Paleoentomofauna Brasileira: Cenário Atual The Brazilian Fossil Insects: Current Scenario Dionizio Angelo de Moura-Júnior; Sandro Marcelo Scheler & Antonio Carlos Sequeira Fernandes Universidade Federal do Rio de Janeiro, Programa de Pós-Graduação em Geociências: Patrimônio Geopaleontológico, Museu Nacional, Quinta da Boa Vista s/nº, São Cristóvão, 20940-040. Rio de Janeiro, RJ, Brasil. E-mails: [email protected]; [email protected]; [email protected] Recebido em: 24/01/2018 Aprovado em: 08/03/2018 DOI: http://dx.doi.org/10.11137/2018_1_142_166 Resumo O presente trabalho fornece um panorama geral sobre o conhecimento da paleoentomologia brasileira até o presente, abordando insetos do Paleozoico, Mesozoico e Cenozoico, incluindo a atualização das espécies publicadas até o momento após a última grande revisão bibliográica, mencionando ainda as unidades geológicas em que ocorrem e os trabalhos relacionados. Palavras-chave: Paleoentomologia; insetos fósseis; Brasil Abstract This paper provides an overview of the Brazilian palaeoentomology, about insects Paleozoic, Mesozoic and Cenozoic, including the review of the published species at the present. It was analiyzed the geological units of occurrence and the related literature. Keywords: Palaeoentomology; fossil insects; Brazil Anuário do Instituto de Geociências - UFRJ 142 ISSN 0101-9759 e-ISSN 1982-3908 - Vol. 41 - 1 / 2018 p. 142-166 A Paleoentomofauna Brasileira: Cenário Atual Dionizio Angelo de Moura-Júnior; Sandro Marcelo Schefler & Antonio Carlos Sequeira Fernandes 1 Introdução Devoniano Superior (Engel & Grimaldi, 2004). Os insetos são um dos primeiros organismos Algumas ordens como Blattodea, Hemiptera, Odonata, Ephemeroptera e Psocopera surgiram a colonizar os ambientes terrestres e aquáticos no Carbonífero com ocorrências até o recente, continentais (Engel & Grimaldi, 2004). -
Hymenoptera) Associated with Crops and Ornamental Plant in Obafemi Awolowo University, Nigeria
International Journal of Zoology and Applied Biosciences ISSN: 2455-9571 Volume 4, Issue 5, pp: 195-206, 2019 http://www.ijzab.com https://doi.org/10.5281/zenodo Research Article DIVERSITY ASSESSMENT OF BEES (HYMENOPTERA) ASSOCIATED WITH CROPS AND ORNAMENTAL PLANT IN OBAFEMI AWOLOWO UNIVERSITY, NIGERIA Oyewole O.A.1, Oyelade O.J.1* and Ogbogu S.S.2 1Natural History Museum, Obafemi Awolowo University, Ile-Ife, Nigeria, 2Department of Zoology, Obafemi Awolowo University, Ile-Ife, Nigeria Article History: Received 16th May 2019; Accepted 27th June 2019; Published 9th October 2019 ABSTRACT This study investigated the various species of bees in the Order Hymenoptera responsible for pollinating crop and ornamental plants in Obafemi Awolowo University (O.A.U.), Ile-Ife, and the study covered habitat preference, abundance and distribution of the bee species in various seasons. This was with a view to identifying and documenting the diversity of bees pollinating agricultural and ornamental plants for a meaningful conservation and management of insects in Nigeria. Bees collection was done using standard sweep net, to collect free range bees species on the sites. Standard yellow pan traps were also set using pineapple as bait to entice bees. Trapped bees were collected and baits were changed on daily basis. The bees were described and identified to species level using existing bee taxonomic keys. Host plants visited by the bee species were identified in the Natural History Museum Herbarium (UNIFEM) and Department of Botany Herbarium (IFE) in Obafemi Awolowo University, Ile-Ife. Paleontological Statistic Software Package (PAST) was used to analyze the collected data. -
Of the Malagasy Subregion (Insecta: Hymenoptera)
download www.zobodat.at Linzer biol. Beitr. 49/1 15-19 28.7.2017 A catalogue of the family Rhopalosomatidae (Vespoidea) of the Malagasy subregion (Insecta: Hymenoptera) Michael MADL A b s t r a c t : In the Malagasy subregion the family Rhopalosomatidae, which is known only from the Madagascar, is represented by the genera Olixon CAMERON, 1887 (two species) and Paniscomima ENDERLEIN, 1904 (four species). K e y w o r d s : Insecta, Hymenoptera, Olixon, Paniscomima, Madagascar. Introduction The family Rhopalosomatidae is known from all zoogeographical regions except the Palaearctic region. In the Malagasy subregion it occurs only on the island of Madagascar. The larvae are parasitods of Orthoptera (Gryllidae), but no host records of the Malagasy species are known. Until now, two species of the genus Olixon CAMERON, 1887 and four species of the genus Paniscomima ENDERLEIN, 1904 have been recorded from Madagascar. How to use the catalogue The systematic part of the catalogue is organized alphabetically. Misidentifications and are marked with an asterisk (*). Only genera described from the Malagasy subregion are mentioned under synonyms and the number of valid species is also restricted to the Malagasy subregion. The known records from Madagascar are listed province by province from North to South and old names or misspellings are in brackets. Abbreviations cat. ......................................................... catalogue descr. ................................................... description ed. ............................................................... -
Review of the Species of Trichomalus (Chalcidoidea: Pteromalidae) Associated with Ceutorhynchus (Coleoptera: Curculionidae) Host Species of European Origin
643 Review of the species of Trichomalus (Chalcidoidea: Pteromalidae) associated with Ceutorhynchus (Coleoptera: Curculionidae) host species of European origin Franck J. Muller CABI Europe—Switzerland, Rue des Grillons 1, 2800 Delémont, Switzerland Hannes Baur Department of Invertebrates, Natural History Museum, Bernastrasse 15, CH-3005 Bern, Switzerland Gary A.P. Gibson, Peter G. Mason Agriculture and Agri-Food Canada, Biodiversity and Integrated Pest Management, Research Centre, 960 Carling Avenue, Ottawa, Canada Ulrich Kuhlmann1 CABI Europe—Switzerland, Rue des Grillons 1, 2800 Delémont, Switzerland Abstract—Six species of Trichomalus Thomson were reared as parasitoids of Ceutorhynchinae hosts in Europe during surveys in 2000–2004. Trichomalus rusticus (Walker) is treated as a valid species, resurrected from synonymy under T. lucidus (Walker), and T. lyttus (Walker) is trans- ferred from synonymy under T. lucidus and newly placed in synonymy with T. rusticus. Illus- trated keys to females and males are given to differentiate the six species (T. bracteatus (Walker), T. campestris (Walker), T. gynetelus (Walker), T. lucidus, T. perfectus (Walker), and T. rusticus) except for males of T. bracteatus and T. gynetelus. A lectotype female is designated for T. rusticus. Trichomalus campestris is newly recorded as a parasitoid of Ceutorhynchus cardariae Korotyaev. Implications of the host–parasitoid associations recovered by the surveys are dis- cussed relative to introduction of species to North America for classical biological control. Résumé—Six espèces de Trichomalus Thomson ont été élevées en tant que parasitoïdes de Ceu- torhynchinae en Europe lors de périodes d’échantillonnage entre 2000 et 2004. Trichomalus rus- ticus (Walker) est traité comme espèce valide et non plus comme synonyme de T. -
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. -
Genomes of the Hymenoptera Michael G
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Digital Repository @ Iowa State University Ecology, Evolution and Organismal Biology Ecology, Evolution and Organismal Biology Publications 2-2018 Genomes of the Hymenoptera Michael G. Branstetter U.S. Department of Agriculture Anna K. Childers U.S. Department of Agriculture Diana Cox-Foster U.S. Department of Agriculture Keith R. Hopper U.S. Department of Agriculture Karen M. Kapheim Utah State University See next page for additional authors Follow this and additional works at: https://lib.dr.iastate.edu/eeob_ag_pubs Part of the Behavior and Ethology Commons, Entomology Commons, and the Genetics and Genomics Commons The ompc lete bibliographic information for this item can be found at https://lib.dr.iastate.edu/ eeob_ag_pubs/269. For information on how to cite this item, please visit http://lib.dr.iastate.edu/ howtocite.html. This Article is brought to you for free and open access by the Ecology, Evolution and Organismal Biology at Iowa State University Digital Repository. It has been accepted for inclusion in Ecology, Evolution and Organismal Biology Publications by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Genomes of the Hymenoptera Abstract Hymenoptera is the second-most sequenced arthropod order, with 52 publically archived genomes (71 with ants, reviewed elsewhere), however these genomes do not capture the breadth of this very diverse order (Figure 1, Table 1). These sequenced genomes represent only 15 of the 97 extant families. Although at least 55 other genomes are in progress in an additional 11 families (see Table 2), stinging wasps represent 35 (67%) of the available and 42 (76%) of the in progress genomes. -
Insect Classification Standards 2020
RECOMMENDED INSECT CLASSIFICATION FOR UGA ENTOMOLOGY CLASSES (2020) In an effort to standardize the hexapod classification systems being taught to our students by our faculty in multiple courses across three UGA campuses, I recommend that the Entomology Department adopts the basic system presented in the following textbook: Triplehorn, C.A. and N.F. Johnson. 2005. Borror and DeLong’s Introduction to the Study of Insects. 7th ed. Thomson Brooks/Cole, Belmont CA, 864 pp. This book was chosen for a variety of reasons. It is widely used in the U.S. as the textbook for Insect Taxonomy classes, including our class at UGA. It focuses on North American taxa. The authors were cautious, presenting changes only after they have been widely accepted by the taxonomic community. Below is an annotated summary of the T&J (2005) classification. Some of the more familiar taxa above the ordinal level are given in caps. Some of the more important and familiar suborders and families are indented and listed beneath each order. Note that this is neither an exhaustive nor representative list of suborders and families. It was provided simply to clarify which taxa are impacted by some of more important classification changes. Please consult T&J (2005) for information about taxa that are not listed below. Unfortunately, T&J (2005) is now badly outdated with respect to some significant classification changes. Therefore, in the classification standard provided below, some well corroborated and broadly accepted updates have been made to their classification scheme. Feel free to contact me if you have any questions about this classification. -
Multifaceted Defense Against Antagonistic Microbes in Developing Offspring of the Parasitoid Wasp Ampulex Compressa (Hymenoptera, Ampulicidae)
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by University of Regensburg Publication Server Multifaceted Defense against Antagonistic Microbes in Developing Offspring of the Parasitoid Wasp Ampulex compressa (Hymenoptera, Ampulicidae) Katharina Weiss, Christopher Parzefall, Gudrun Herzner* Evolutionary Ecology Group, Institute of Zoology, University of Regensburg, Regensburg, Germany Abstract Effective antimicrobial strategies are essential adaptations of insects to protect themselves, their offspring, and their foods from microbial pathogens and decomposers. Larvae of the emerald cockroach wasp, Ampulex compressa, sanitize their cockroach hosts, Periplaneta americana, with a cocktail of nine antimicrobials comprising mainly (R)-(-)-mellein and micromolide. The blend of these antimicrobials has broad-spectrum antimicrobial activity. Here we explore the spatio- temporal pattern of deployment of antimicrobials during the development from egg to adult as well as their physico- chemical properties to assess how these aspects may contribute to the success of the antimicrobial strategy. Using gas chromatography/mass spectrometry (GC/MS) we show that larvae start sanitizing their food as soon as they have entered their host to feed on its tissue. Subsequently, they impregnate the cockroach carcass with antimicrobials to create a hygienic substrate for cocoon spinning inside the host. Finally, the antimicrobials are incorporated into the cocoon. The antimicrobial profiles on cockroach and wasp cocoon differed markedly. While micromolide persisted on the cockroaches until emergence of the wasps, solid-phase microextraction sampling and GC/MS analysis revealed that (R)-(-)-mellein vaporized from the cockroaches and accumulated in the enclosed nest. In microbial challenge assays (R)-(-)-mellein in the headspace of parasitized cockroaches inhibited growth of entomopathogenic and opportunistic microbes (Serratia marcescens, Aspergillus sydowii, Metarhizium brunneum). -
Os Nomes Galegos Dos Insectos 2020 2ª Ed
Os nomes galegos dos insectos 2020 2ª ed. Citación recomendada / Recommended citation: A Chave (20202): Os nomes galegos dos insectos. Xinzo de Limia (Ourense): A Chave. https://www.achave.ga /wp!content/up oads/achave_osnomesga egosdos"insectos"2020.pd# Fotografía: abella (Apis mellifera ). Autor: Jordi Bas. $sta o%ra est& su'eita a unha licenza Creative Commons de uso a%erto( con reco)ecemento da autor*a e sen o%ra derivada nin usos comerciais. +esumo da licenza: https://creativecommons.org/ icences/%,!nc-nd/-.0/deed.g . 1 Notas introdutorias O que cont n este documento Na primeira edición deste recurso léxico (2018) fornecéronse denominacións para as especies máis coñecidas de insectos galegos (e) ou europeos, e tamén para algúns insectos exóticos (mostrados en ám itos divulgativos polo seu interese iolóxico, agr"cola, sil!"cola, médico ou industrial, ou por seren moi comúns noutras áreas xeográficas)# Nesta segunda edición (2020) incorpórase o logo da $%a!e ao deseño do documento, corr"xese algunha gralla, reescr" ense as notas introdutorias e engádense algunhas especies e algún nome galego máis# &n total, ac%éganse nomes galegos para 89( especies de insectos# No planeta téñense descrito aproximadamente un millón de especies, e moitas están a"nda por descubrir# Na )en"nsula * érica %a itan preto de +0#000 insectos diferentes# Os nomes das ol oretas non se inclúen neste recurso léxico da $%a!e, foron o xecto doutro tra allo e preséntanse noutro documento da $%a!e dedicado exclusivamente ás ol oretas, a!ela"ñas e trazas . Os nomes galegos