OTHER BEES and WASPS Advanced Level Training Texas Master Beekeeper Program
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Hornets Have It
Hornets have it: a conserved olfactory subsystem for social recognition in hymenoptera? Antoine Couto, Aniruddha Mitra, Denis Thiery, Frédéric Marion-Poll, Jean-Christophe Sandoz To cite this version: Antoine Couto, Aniruddha Mitra, Denis Thiery, Frédéric Marion-Poll, Jean-Christophe Sandoz. Hor- nets have it: a conserved olfactory subsystem for social recognition in hymenoptera?. Frontiers in Neuroanatomy, Frontiers, 2017, 11, 10.3389/fnana.2017.00048. hal-01605044 HAL Id: hal-01605044 https://hal.archives-ouvertes.fr/hal-01605044 Submitted on 26 May 2020 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. Distributed under a Creative Commons Attribution| 4.0 International License ORIGINAL RESEARCH published: 14 June 2017 doi: 10.3389/fnana.2017.00048 Hornets Have It: A Conserved Olfactory Subsystem for Social Recognition in Hymenoptera? Antoine Couto 1, Aniruddha Mitra 1, Denis Thiéry 2, Frédéric Marion-Poll 1 and Jean-Christophe Sandoz 1* 1 Evolution Genomes Behavior and Ecology, Centre National de la Recherche Scientifique, Univ Paris-Sud, IRD, Université Paris Saclay, Gif-sur-Yvette, France, 2 UMR 1065 Santé et Agroécologie du Vignoble, INRA, Université de Bordeaux, ISVV, Villenave d’Ornon, France Eusocial Hymenoptera colonies are characterized by the presence of altruistic individuals, which rear their siblings instead of their own offspring. -
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. -
Diptera: Syrphidae
This is a repository copy of The relationship between morphological and behavioral mimicry in hover flies (Diptera: Syrphidae).. White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/80035/ Version: Accepted Version Article: Penney, HD, Hassall, C orcid.org/0000-0002-3510-0728, Skevington, JH et al. (2 more authors) (2014) The relationship between morphological and behavioral mimicry in hover flies (Diptera: Syrphidae). The American Naturalist, 183 (2). pp. 281-289. ISSN 0003-0147 https://doi.org/10.1086/674612 Reuse Unless indicated otherwise, fulltext items are protected by copyright with all rights reserved. The copyright exception in section 29 of the Copyright, Designs and Patents Act 1988 allows the making of a single copy solely for the purpose of non-commercial research or private study within the limits of fair dealing. The publisher or other rights-holder may allow further reproduction and re-use of this version - refer to the White Rose Research Online record for this item. Where records identify the publisher as the copyright holder, users can verify any specific terms of use on the publisher’s website. Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ The relationship between morphological and behavioral mimicry in hover flies (Diptera: Syrphidae)1 Heather D. Penney, Christopher Hassall, Jeffrey H. Skevington, Brent Lamborn & Thomas N. Sherratt Abstract Palatable (Batesian) mimics of unprofitable models could use behavioral mimicry to compensate for the ease with which they can be visually discriminated, or to augment an already close morphological resemblance. -
Insect Biodiversity at Mangrove Ecosystem
108 Insect Biodiversity At Mangrove Ecosystem Bhagyashree Grampurohit1 and Hemant Karkhanis2 1Department of Environmental Science, K. J. Somaiya College of Science and Commerce, Mumbai Vidyavihar, Mumbai -400077, Ph. +91-022-28575590, Fax +91-022 28575670 2 IInd Floor, Udayachal Primary School, Vikhroli (E). Email: [email protected]; [email protected] Abstract : A lot of attention being paid to the study of biodiversity has led to increasing interest in assessing the diversity of insects because this group dominates terrestrial and freshwater ecosystems and are valuable indicators of the healthof these ecosystems. Presence of insects in the mangrove ecosystem is of importance because they feed, reproduce on plants and help in pollination. Certain level of natural damage caused by pest insects is of ecological significance in mangrove ecosystem. Study of insect biodiversity is useful in managing the forest resources. The study area selected for this research project is a private land owned by Godrej & Boyce Mfg.Co.Ltd located along the Eastern Express Highway at Vikhroli, Mumbai. This land is covered with mangrove forest. Total eleven sites were selected randomly so as to cover maximum area of mangrove forest. At each site, during low tide, different insects were observed and photographed. Photo-essay of these insects was prepared. Diversity index, evenness index and dominance index was calculated. As per the results, Shannon index is 0.4, Simphon’s diversity index is 0.93 and evenness index is 0.1. Species richness index is 1.94. The result shows that the study location being in the industrial area of Mumbai, the insect diversity is less but there is a natural balance of damage and reproduction. -
Wedge-Shaped Beetles (Suggested Common Name) Ripiphorus Spp. (Insecta: Coleoptera: Ripiphoridae)1 David Owens, Ashley N
EENY613 Wedge-Shaped Beetles (suggested common name) Ripiphorus spp. (Insecta: Coleoptera: Ripiphoridae)1 David Owens, Ashley N. Mortensen, Jeanette Klopchin, William Kern, and Jamie D. Ellis2 Introduction Ripiphoridae are a family of unusual parasitic beetles that are thought to be related to tumbling flower beetles (Coleoptera: Mordellidae) and blister beetles (Coleoptera: Meloidae). There is disagreement over the spelling of the family (Ripiphoridae) and genus (Ripiphorus) names. Here we use the original spelling that starts with only the letter Figure 1. Adult specimens of the two genera of Ripiphoridae. A) “R”; however, an initial “Rh” has also been used in the Macrosiagon Hentz, and B) Ripiphorus Bosc. scientific community (Rhipiphoridae and Rhipiphorus). Credits: Allen M. Boatman There are an estimated 35 nearctic species of Ripiphorus, Generally, the biology of the family Ripiphoridae is poorly two of which have been collected in Florida: Ripiphorus known. Ripiphorids parasitize bees and wasps (Hymenop- schwarzi LeConte (Figure 2A) and Ripiphorus fasciatus Say tera), roaches (Blattodea), and wood-boring beetles (Co- (Figure 2B). Due to limited information for both of these leoptera). However, the specific hosts for many ripiphorid species, the information presented below is characteristic species are unknown. Furthermore, only one sex (either of the genus Ripiphorus. Information specific to Ripiphorus male or female) has been described for several species, and fasciatus and Ripiphorus schwarzi is presented where the males and females of some species look different. detailed information is available. Two genera of Ripiphoridae infest hymenopteran (bee and wasp) nests: Macrosiagon Hentz (Figure 1A) and Ripiphorus Bosc (formerly Myodites Latreille) (Figure 1B). Species of Macrosiagon are parasites of a variety of hymenopteran families including: Halictidae, Vespidae, Tiphiidae, Apidae, Pompilidae, Crabronidae, and Sphecidae. -
The Conservation Management and Ecology of Northeastern North
THE CONSERVATION MANAGEMENT AND ECOLOGY OF NORTHEASTERN NORTH AMERICAN BUMBLE BEES AMANDA LICZNER A DISSERTATION SUBMITTED TO THE FACULTY OF GRADUATE STUDIES IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY GRADUATE PROGRAM IN BIOLOGY YORK UNIVERSITY TORONTO, ONTARIO September 2020 © Amanda Liczner, 2020 ii Abstract Bumble bees (Bombus spp.; Apidae) are among the pollinators most in decline globally with a main cause being habitat loss. Habitat requirements for bumble bees are poorly understood presenting a research gap. The purpose of my dissertation is to characterize the habitat of bumble bees at different spatial scales using: a systematic literature review of bumble bee nesting and overwintering habitat globally (Chapter 1); surveys of local and landcover variables for two at-risk bumble bee species (Bombus terricola, and B. pensylvanicus) in southern Ontario (Chapter 2); identification of conservation priority areas for bumble bee species in Canada (Chapter 3); and an analysis of the methodology for locating bumble bee nests using detection dogs (Chapter 4). The main findings were current literature on bumble bee nesting and overwintering habitat is limited and biased towards the United Kingdom and agricultural habitats (Ch.1). Bumble bees overwinter underground, often on shaded banks or near trees. Nests were mostly underground and found in many landscapes (Ch.1). B. terricola and B. pensylvanicus have distinct habitat characteristics (Ch.2). Landscape predictors explained more variation in the species data than local or floral resources (Ch.2). Among local variables, floral resources were consistently important throughout the season (Ch.2). Most bumble bee conservation priority areas are in western Canada, southern Ontario, southern Quebec and across the Maritimes and are most often located within woody savannas (Ch.3). -
Scottish Bees
Scottish Bees Introduction to bees Bees are fascinating insects that can be found in a broad range of habitats from urban gardens to grasslands and wetlands. There are over 270 species of bee in the UK in 6 families - 115 of these have been recorded in Scotland, with 4 species now thought to be extinct and insufficient data available for another 2 species. Bees are very diverse, varying in size, tongue-length and flower preference. In the UK we have 1 species of honey bee, 24 species of bumblebee and the rest are solitary bees. They fulfil an essential ecological and environmental role as one of the most significant groups of pollinating insects, all of which we depend upon for the pollination of 80% of our wild and cultivated plants. Some flowers are in fact designed specifically for bee pollination, to the exclusion of generalist pollinators. Bees and their relatives Bees are classified in the complex insect order Hymenoptera (meaning membrane-winged), which also includes many kinds of parasitic wasps, gall wasps, hunting wasps, ants and sawflies. There are about 150,000 species of Hymenoptera known worldwide separated into two sub-orders. The first is the most primitive sub-order Symphyta which includes the sawflies and their relatives, lacking a wasp-waist and generally with free-living caterpillar-like larvae. The second is the sub-order Apocrita, which includes the ants, bees and wasps which are ’wasp-waisted’ and have grub-like larvae that develop within hosts, galls or nests. The sub-order Apocrita is in turn divided into two sections, the Parasitica and Aculeata. -
Natural Resource Inventory Smith-Sargent
NATURAL RESOURCE INVENTORY of the SMITH-SARGENT ROAD PROPERTY Holderness, NH FINAL REPORT [Smith-Sargent Property Upper Marsh as seen from south boundary] Compiled by: Dr. Rick Van de Poll Ecosystem Management Consultants 30 N. Sandwich Rd. Center Sandwich, NH 03227 603-284-6851 [email protected] Submitted to: Holderness Conservation Commission June 30, 2016 i SUMMARY Between October 2015 and June 2016 a comprehensive natural resources inventory (NRI) was completed by Ecosystem Management Consultants (EMC) of Sandwich, NH on the 8.5-acre town conservation land at the corner of Sargent Road and Smith Road in Holderness, NH. Managed by the Holderness Conservation Commission (HCC), this parcel was obtained largely for the complex wetland system that occupies more than 65% of the parcel. The purpose of the NRI was to inform the town about the qualities of the natural resources on the lot, as well as to determine whether or not the site would be suitable for limited environmental education for the general public. Three site visits were conducted at the Sargent-Smith Road Property for the purpose of gathering NRI data. A fourth visit was also made on November 15, 2015 for the purpose of educating the HCC and other town officials about the extent and functional value of the wetlands on the parcel. The first field visit in October provided an initial review of the location of the parcel, the boundary of the wetland, and the plant and animal resources present. A second site visit in January was held for the purpose of tracking mammals during good snow cover. -
Wasp and Bee Management a Common-Sense Approach
NRAES-185 Wasp and Bee Management A Common-Sense Approach Jody Gangloff-Kaufmann NRAES-185 Recycled Paper NRAES-185 Wasp and Bee Management A Common-Sense Approach Written by Jody Gangloff-Kaufmann New York State IPM Program Cornell University NRAES–185 October 2011 © 2011 by NRAES (Natural Resource, Agriculture, and Engineering Service). All rights reserved. Inquiries invited. ISBN 978-1-933395-22-7 Library of Congress Cataloging-in-Publication Data Gangloff-Kaufmann, Jody Lynn Wasp and bee management : a common-sense approach / Jody Gangloff-Kaufmann. p. cm. -- (NRAES ; 185) Includes bibliographical references. ISBN 978-1-933395-22-7 1. Wasps. 2. Bees. 3. Wasps--Integrated control. 4. Bees--Integrated control. I. Natural Resource, Agriculture, and Engineering Service. Cooperative Extension. II. Title. III. Series: NRAES (Series) ; 185. SB945.W3G36 2011 632’.79--dc23 2011023501 Disclaimer Mention of a trademark, proprietary product, or commercial firm in text or figures does not constitute an endorsement by the Cooperative Extension System or the publisher and does not imply approval to the exclusion of other suitable products or firms. Requests to reprint parts of this publication should be sent to NRAES. In your request, please state which parts of the publication you would like to reprint and describe how you intend to use the material. Contact NRAES if you have any questions. To order additional copies, contact: Natural Resource, Agriculture, and Engineering Service (NRAES) Cooperative Extension PO Box 4557, Ithaca, New York 14852-4557 Phone: (607) 255-7654 • Fax: (607) 254-8770 Email: [email protected] • Web site: www.nraes.org Cover photo: A female Carpenter bee, T. -
Scientific Notes 193 APPLICATION of ALARM PHEROMONE TO
Scientific Notes 193 APPLICATION OF ALARM PHEROMONE TO TARGETS BY SOUTHERN YELLOWJACKETS (HYMENOPTERA: VESPIDAE) HAL C. REED1 AND PETER J. LANDOLT USDA, ARS, 5230 Konnowac Pass Rd., Wapato, WA 98951, USA 1Current address: Department of Biology, Oral Roberts University, Tulsa, OK 74171 Alarm pheromones have been demonstrated for a number of species of social Vesp- idae including several hornets and yellowjackets (Vespines) (Landolt et al. 1997). Maschwitz (1964a, b) first demonstrated alarm pheromone responses in the yellow- jackets Vespula vulgaris L. and V. germanica (Fab.) in response to crushed wasps and body parts. Pheromone-mediated alarm has since been observed in other vespines: Dolichovespula saxonica (Fab.) (Maschwitz 1984), the southern yellowjacket V. squa- mosa (Drury) (Landolt & Heath 1987, Landolt et al. 1999), the eastern yellowjacket V. maculifrons (Buysson) (Landolt et al. 1995), Provespa anomala Saussure (Maschwitz & Hanel 1988), and Vespa crabro L. (Veith et al. 1984). 2-Methyl-3- butene-2-ol was identified as a component of the alarm pheromone of V. crabro (Veith et al. 1984), and N-3- methylbutylacetamide was isolated and identified as an alarm pheromone of the southern and eastern yellowjackets (Heath & Landolt 1988, Landolt et al. 1995). The source of alarm pheromones in social wasps generally is the venom, although the head is implicated as an additional source of alarm pheromone for V. vulgaris (Al- diss 1983) and V. squamosa (Landolt et al. 1999). Alarm behavior in V. germanica and V. vulgaris occurred in response to the squashed sting apparatus, sting sac, and sol- vent extract of the sting sac (Maschwitz 1964b) and in D. -
Bald-Faced Hornets
Pest Profile Photo credit: By PiccoloNamek (http://www.gnu.org/copyleft/fdl.html), CC-BY-SA-3.0 (http://creativecommons.org/licenses/by-sa/3.0/) from Wikimedia Commons Common Name: Bald Faced Hornet Scientific Name: Dolichovespula maculata Order and Family: Hymenoptera: Vespidae Size and Appearance: Bald faced hornets range in size from about 15 to over 20 mm in length with queens being up to 25% larger. They receive their common name from the unique white pattern present on the black face of the adults. The females also feature 2 stripes on the thorax and on the last 3 abdominal segments as well. The rest of the body tends to be a dull grey in color. Length (mm) Appearance Egg 1 mm 1 egg is laid per gallery cell. Larval and pupal stages take place entirely in gallery. Nests are aerial and usually contain 2,000 cells. Larva/Nymph 10-22 in length depending on White, cylindrical. Remain in instar and species cells in paper nests through pupation. Adult 15-20+ mm long Gray to black in overall coloration with white markings on face. Females have white stripes on thorax and abdominal segments. Pupa (if applicable) 10-25 mm long Light colored, made of final larval skin. Formed inside of gallery cell. Type of feeder (Chewing, sucking, etc.): Chewing Host /s: Dolichovespula maculata consume various arthropods, many of which are pests. They are considered beneficial for this reason. Description of Damage (larvae and adults): Though they do a positive service by consuming pest species, if a nest is nearby a home, their aggressive nature leads to stings for humans and pets. -
Kenai National Wildlife Refuge Species List, Version 2018-07-24
Kenai National Wildlife Refuge Species List, version 2018-07-24 Kenai National Wildlife Refuge biology staff July 24, 2018 2 Cover image: map of 16,213 georeferenced occurrence records included in the checklist. Contents Contents 3 Introduction 5 Purpose............................................................ 5 About the list......................................................... 5 Acknowledgments....................................................... 5 Native species 7 Vertebrates .......................................................... 7 Invertebrates ......................................................... 55 Vascular Plants........................................................ 91 Bryophytes ..........................................................164 Other Plants .........................................................171 Chromista...........................................................171 Fungi .............................................................173 Protozoans ..........................................................186 Non-native species 187 Vertebrates ..........................................................187 Invertebrates .........................................................187 Vascular Plants........................................................190 Extirpated species 207 Vertebrates ..........................................................207 Vascular Plants........................................................207 Change log 211 References 213 Index 215 3 Introduction Purpose to avoid implying