An Annotated List of Bees (Hymenoptera: Apoidea: Apiformis) of Sri Lanka
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5.4 Insect Visitors to Marianthus Aquilonaris and Surrounding Flora
REPORT: Insect visitors to Marianthus aquilonaris and surrounding flora Nov 2-4, 2019 Kit Prendergast, Native bee scientist BSc First Class Honours, PhD researcher and Forrest Scholar On behalf of Botanica Consulting 1 REPORT: Insect visitors to Marianthus aquilonaris and surrounding flora Nov 2-4 2019 Kit Prendergast, Native bee scientist Background Marianthus aquilonaris (Fig. 1) was declared as Rare Flora under the Western Australian Wildlife Conservation Act 1950 in 2002 under the name Marianthus sp. Bremer, and is ranked as Critically Endangered (CR) under the International Union for Conservation of Nature (IUCN 2001) criteria B1ab(iii,v)+2ab(iii,v); C2a(ii) due to its extent of occurrence being less than 100 km2, its area of occupancy being less than 10 km2, a continuing decline in the area, extent and/or quality of its habitat and number of mature individuals and there being less than 250 mature individuals known at the time of ranking (Appendix A). However, it no longer meets these criteria as more plants have been found, and a recommendation has been proposed to be made by DBCA to the Threatened Species Scientific Committee (TSSC) to change its conservation status to CR B1ab(iii,v)+2ab(iii,v) (Appendix A), but this recommendation has not gone ahead (DEC, 2010). Despite its listing as CR under the Western Australian Biodiversity Conservation Act 2016, the species is not currently listed under the Environment Protection and Biodiversity Conservation Act 1999. The main threats to the species are mining/exploration, track maintenance and inappropriate fire regimes (DEC, 2010). Fig. 1. Marianthus aquilonaris, showing flower, buds and leaves. -
Wild Bee Species Increase Tomato Production and Respond Differently to Surrounding Land Use in Northern California
BIOLOGICAL CONSERVATION 133 (2006) 81– 87 available at www.sciencedirect.com journal homepage: www.elsevier.com/locate/biocon Wild bee species increase tomato production and respond differently to surrounding land use in Northern California Sarah S. Greenleaf*, Claire Kremen1 Department of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, United States ARTICLE INFO ABSTRACT Article history: Pollination provided by bees enhances the production of many crops. However, the contri- Received 11 December 2005 bution of wild bees remains unmeasured for many crops, and the effects of anthropogenic Received in revised form change on many bee species are unstudied. We experimentally investigated how pollina- 5 May 2006 tion by wild bees affects tomato production in northern California. We found that wild bees Accepted 16 May 2006 substantially increase the production of field-grown tomato, a crop generally considered Available online 24 July 2006 self-pollinating. Surveys of the bee community on 14 organic fields that varied in proximity to natural habitat showed that the primary bee visitors, Anthophora urbana Cresson and Keywords: Bombus vosnesenskii Radoszkowski, were affected differently by land management prac- Agro-ecosystem tices. B. vosnesenskii was found primarily on farms proximate to natural habitats, but nei- Crop pollination ther proximity to natural habitat nor tomato floral abundance, temperature, or year Ecosystem services explained variation in the visitation rates of A. urbana. Natural habitat appears to increase Bombus vosnesenskii B. vosnesenskii populations and should be preserved near farms. Additional research is Anthophora urbana needed to determine how to maintain A. urbana. Species-specific differences in depen- Habitat conservation dency on natural habitats underscore the importance of considering the natural histories of individual bee species when projecting population trends of pollinators and designing management plans for pollination services. -
SPECIES COMPOSITION and POLLINATOR EFFICIENCY of Ocimum Kilimandscharicum FLOWER VISITORS ALONG KAKAMEGA FOREST ECOSYSTEM
SPECIES COMPOSITION AND POLLINATOR EFFICIENCY OF Ocimum Kilimandscharicum FLOWER VISITORS ALONG KAKAMEGA FOREST ECOSYSTEM BY HELLEN MANDELA KUTWA A Research Thesis Submitted in Partial Fulfillment of the Requirements for the Award of the Degree of Masters of Science in Environmental Biology, School of Biological and Physical Sciences MOI UNIVERSITY ELDORET 2017 2 ECLARATION 3 DEDICATION I dedicate this work to my parents who have supported me throughout, Dr Amos Kutwa and Mrs. Phillisters Kutwa. To my siblings Alice, Erastus and Fred I hope this serves as a source of inspiration and reassurance that hard work and persistence pays out. My grandparents Alice, Hellen and Silvanas for their prayers and encouragement. 4 ACKNOWLEDGEMENT I am grateful to Professor Mugatsia Tsingalia for having accepted to be my University supervisor and providing me with high quality assistance and guidance. You have been a source of motivation from the beginning and I truly appreciate your patience especially when I had no sense of direction and you guided me and molded me into a better researcher. I am thankful as you have always been that academic lighthouse for me. I also recognize the Moi University fraternity especially School of Biological and Physical science for seeing potential in me and accepting my postgraduate application. I am also greatly indebted to Professor Mary Gikungu. You have always been encouraging from the beginning setting a fine example for me as a strong independent woman. You helped instill in me the importance of being resilient and humble no matter what you have achieved. You encouraged me even when I was about to give up, taking your time to go through my drafts and giving critical and up building comments. -
A Visual Guide for the Identification of British Coelioxys Bees
1 Introduction The Hymenoptera is an order of insects that includes bees, wasps, ants, ichneumons, sawflies, gall wasps and their relatives. The bees (family Apidae) can be recognised as such by the presence of feather-like hairs on their bodies, particularly near the wing bases. The genus Coelioxys Latreille belongs to the bee subfamily Megachilinae. There are six species of Coelioxys present in mainland Britain. Two other species are found in Guernsey but not mentioned in this pictorial key (C. afra Lepeletier and C. brevis Eversmann). Natural History Coelioxys (their various English names are: Sharp-tailed Bees, Sharp-abdomen Bees and Sharp-bellied Bees) are among those known as cuckoo bees because the larvae grow up on food stolen from Leaf-cutter Bees (Megachile Latreille) or Flower Bees (Anthophora Latreille). The genus Megachile probably includes the closest relatives of Coelioxys. Female Megachile construct nests of larval cells from leaves and provision each cell with a mixture of pollen and nectar for the young. A female Coelioxys will seek these out and apparently uses its sharp abdomen to pierce the cells. An egg is then laid in the Megachile cell. The egg of the Coelioxys hatches before that of the Megachile and the newly-hatched larva crushes the Megachile egg with its large jaws. The Coelioxys larva can then feed on the contents of the cell. Pupation occurs within a cocoon spun within the host cell where the larva overwinters as a prepupa. The genus Anthophora excavates nest burrows in sandy soil or rotting wood, where they may also become the hosts of Coelioxys larvae. -
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, -
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 . -
Pollination of Cultivated Plants in the Tropics 111 Rrun.-Co Lcfcnow!Cdgmencle
ISSN 1010-1365 0 AGRICULTURAL Pollination of SERVICES cultivated plants BUL IN in the tropics 118 Food and Agriculture Organization of the United Nations FAO 6-lina AGRICULTUTZ4U. ionof SERNES cultivated plans in tetropics Edited by David W. Roubik Smithsonian Tropical Research Institute Balboa, Panama Food and Agriculture Organization of the United Nations F'Ø Rome, 1995 The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization of the United Nations concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. M-11 ISBN 92-5-103659-4 All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photocopying or otherwise, without the prior permission of the copyright owner. Applications for such permission, with a statement of the purpose and extent of the reproduction, should be addressed to the Director, Publications Division, Food and Agriculture Organization of the United Nations, Viale delle Terme di Caracalla, 00100 Rome, Italy. FAO 1995 PlELi. uion are ted PlauAr David W. Roubilli (edita Footli-anal ISgt-iieulture Organization of the Untled Nations Contributors Marco Accorti Makhdzir Mardan Istituto Sperimentale per la Zoologia Agraria Universiti Pertanian Malaysia Cascine del Ricci° Malaysian Bee Research Development Team 50125 Firenze, Italy 43400 Serdang, Selangor, Malaysia Stephen L. Buchmann John K. S. Mbaya United States Department of Agriculture National Beekeeping Station Carl Hayden Bee Research Center P. -
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. -
Intro Outline
THE REPRODUCTIVE ECOLOGY OF TWO TERRESTRIAL ORCHIDS, CALADENIA RIGIDA AND CALADENIA TENTACULATA RENATE FAAST Submitted for the degree of Doctor of Philosophy School of Earth and Environmental Sciences The University of Adelaide, South Australia December, 2009 i . DEcLARATION This work contains no material which has been accepted for the award of any other degree or diploma in any university or other tertiary institution to Renate Faast and, to the best of my knowledge and belief, contains no material previously published or written by another person, except where due reference has been made in the text. I give consent to this copy of my thesis when deposited in the University Library, being made available for loan and photocopying, subject to the provisions of the Copyright Act 1968. The author acknowledges that copyright of published works contained within this thesis (as listed below) resides with the copyright holder(s) of those works. I also give permission for the digital version of my thesis to be made available on the web, via the University's digital research repository, the Library catalogue, the Australasian Digital Theses Program (ADTP) and also through web search engines. Published works contained within this thesis: Faast R, Farrington L, Facelli JM, Austin AD (2009) Bees and white spiders: unravelling the pollination' syndrome of C aladenia ri gída (Orchidaceae). Australian Joumal of Botany 57:315-325. Faast R, Facelli JM (2009) Grazrngorchids: impact of florivory on two species of Calademz (Orchidaceae). Australian Journal of Botany 57:361-372. Farrington L, Macgillivray P, Faast R, Austin AD (2009) Evaluating molecular tools for Calad,enia (Orchidaceae) species identification. -
Discovery of Megachile (Pseudomegachile) Lanata (Fabricius, 1775) (Hymenoptera, Megachilidae) in Colombia, an Adventive Bee Species from the Old World
15 1 NOTES ON GEOGRAPHIC DISTRIBUTION Check List 15 (1): 45–48 https://doi.org/10.15560/15.1.45 Discovery of Megachile (Pseudomegachile) lanata (Fabricius, 1775) (Hymenoptera, Megachilidae) in Colombia, an adventive bee species from the Old World Victor H. Gonzalez1, Diego A. Guevara2, Joanna Jaramillo-Silva2, Rodulfo Ospina2 1 Undergraduate Biology Program and Department of Ecology and Evolutionary Biology, Haworth Hall, 1200 Sunnyside Ave., University of Kansas, Lawrence, KS, 66045, USA. 2 Laboratorio de Investigaciones en Abejas, Departamento de Biología, Universidad Nacional de Colombia, Bogotá, DC; [email protected], [email protected], [email protected] Corresponding author: Victor H. Gonzalez, [email protected] Abstract We record for the first time for Colombia Megachile (Pseudomegachile) lanata (Fabricius, 1775), a bee species from Southeast Asia. This is the first record of an adventive bee species for the country besides Apis mellifera Linnaeus, 1758, the European honey bee. Megachile lanata appears to have arrived to the Caribbean coast of Colombia nearly half a century ago, reaching the Orinoquia region recently. We provide comments on diagnostic features to facilitate the recognition of this bee species and discuss its possible establishment in Colombia. Key words Conservation, dauber bees, invasive species, Megachilini, pollinators. Academic editor: Gabriela P. Camacho | Received 6 October 2018 | Accepted 18 December 2018 | Published 18 January 2019 Citation: Gonzalez VH, Guevara DA, Jaramillo-Silva J, Ospina R (2019) Discovery of Megachile (Pseudomegachile) lanata (Fabricius, 1775) (Hymenoptera, Megachilidae) in Colombia, an adventive bee species from the Old World. Check List 15 (1): 45–48. https://doi.org/10.15560/15.1.45 Introduction cosmopolitan in distribution, as in the case of the European honey bees and the wool carder bee Anthid- A few bee species, such as the European honey bee ium manicatum (Linnaeus, 1758) (e.g., Gonzalez et al. -
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. -
Identification of 37 Microsatellite Loci for Anthophora Plumipes (Hymenoptera: Apidae) Using Next Generation Sequencing and Their Utility in Related Species
Eur. J. Entomol. 109: 155–160, 2012 http://www.eje.cz/scripts/viewabstract.php?abstract=1692 ISSN 1210-5759 (print), 1802-8829 (online) Identification of 37 microsatellite loci for Anthophora plumipes (Hymenoptera: Apidae) using next generation sequencing and their utility in related species KATEěINA ýERNÁ and JAKUB STRAKA Department of Zoology, Faculty of Science, Charles University in Prague, Viniþná 7, 128 43 Praha 2, Czech Republic; e-mails: [email protected]; [email protected] Key words. Hymenoptera, Apidae, microsatellite development, Anthophora plumipes, 454 sequencing, Anthophorini Abstract. Novel microsatellite markers for the solitary bee, Anthophora plumipes, were identified and characterised using 454 GS-FLX Titanium pyrosequencing technology. Thirty seven loci were tested using fluorescently labelled primers on a sample of 20 females from Prague. The number of alleles ranged from 1 to 10 (with a mean of 4 alleles per locus), resulting in an observed hetero- zygosity ranging from 0.05 to 0.9 and an expected heterozygosity from 0.097 to 0.887. None of the loci showed a significant devia- tion from the Hardy-Weinberg equilibrium and only two loci showed the significant presence of null alleles. No linkage between loci was detected. We further provide information on a single multiplex PCR consisting of 11 of the most polymorphic loci. This multi- plex approach provides an effective analytical tool for analysing genetic structure and carrying out parental analyses on Anthophora populations. Most of the 37 loci tested also showed robust amplification in five other Anthophora species (A. aestivalis, A. crinipes, A. plagiata, A. pubescens and A. quadrimaculata).