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Male and Female Bees Show Large Differences in Floral Preference
bioRxiv preprint doi: https://doi.org/10.1101/432518; this version posted November 16, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 Male and female bees show large differences in floral preference 2 3 Michael Roswell [email protected] 4 Graduate program in ecology and evolution, Rutgers University 5 14 College Farm Road, New Brunswick, NJ 08904 6 7 Jonathan Dushoff 8 Department of biology, McMaster University 9 1280 Main St. West, Hamilton, Ontario ON L8S 4K1 10 11 Rachael Winfree 12 Department of ecology, evolution, and natural resources, Rutgers University 13 14 College Farm Road, New Brunswick, NJ 08904 1 bioRxiv preprint doi: https://doi.org/10.1101/432518; this version posted November 16, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 14 Abstract 15 16 1. Intraspecific variation in foraging niche can drive food web dynamics and 17 ecosystem processes. Field studies and theoretical analysis of plant-pollinator 18 interaction networks typically focus on the partitioning of the floral community 19 between pollinator species, with little attention paid to intraspecific variation 20 among plants or foraging bees. In other systems, male and female animals 21 exhibit different, cascading, impacts on interaction partners. -
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. -
The Digger Wasps of Saudi Arabia: New Records and Distribution, with a Checklist of Species (Hym.: Ampulicidae, Crabronidae and Sphecidae)
NORTH-WESTERN JOURNAL OF ZOOLOGY 9 (2): 345-364 ©NwjZ, Oradea, Romania, 2013 Article No.: 131206 http://biozoojournals.3x.ro/nwjz/index.html The digger wasps of Saudi Arabia: New records and distribution, with a checklist of species (Hym.: Ampulicidae, Crabronidae and Sphecidae) Neveen S. GADALLAH1,*, Hathal M. AL DHAFER2, Yousif N. ALDRYHIM2, Hassan H. FADL2 and Ali A. ELGHARBAWY2 1. Entomology Department, Faculty of Science, Cairo University, Giza, Egypt. 2. Plant Protection Department, College of Food and Agriculture Science, King Saud University, King Saud Museum of Arthropod (KSMA), Riyadh, Saudi Arabia. *Corresponing author, N.S. Gadalah, E-mail: [email protected] Received: 24. September 2012 / Accepted: 13. January 2013 / Available online: 02. June 2013 / Printed: December 2013 Abstract. The “sphecid’ fauna of Saudi Arabia (Hymenoptera: Apoidea) is listed. A total of 207 species in 42 genera are recorded including previous and new species records. Most Saudi Arabian species recorded up to now are more or less common and widespread mainly in the Afrotropical and Palaearctic zoogeographical zones, the exception being Bembix buettikeri Guichard, Bembix hofufensis Guichard, Bembix saudi Guichard, Cerceris constricta Guichard, Oxybelus lanceolatus Gerstaecker, Palarus arabicus Pulawski in Pulawski & Prentice, Tachytes arabicus Guichard and Tachytes fidelis Pulawski, which are presumed endemic to Saudi Arabia (3.9% of the total number of species). General distribution and ecozones, and Saudi Arabian localities are given for each species. In this study two genera (Diodontus Curtis and Dryudella Spinola) and 11 species are newly recorded from Saudi Arabia. Key words: Ampulicidae, Crabronidae, Sphecidae, faunistic list, new records, Saudi Arabia. Introduction tata boops (Schrank), Bembecinus meridionalis A.Costa, Diodontus sp. -
Hymenoptera: Apoidea) Ở Miền Bắc, Việt Nam
KỶ YẾU HỘI NGHỊ KHOA HỌC 45 NĂM VIỆN HÀN LÂM KHCNVN DOI: 10.15625/vap.2020.00128 NGHIÊN CỨU THÀNH PHẦN VÀ SỰ PHÂN BỐ CỦA CÁC LOÀI ONG MẬT (HYMENOPTERA: APOIDEA) Ở MIỀN BẮC, VIỆT NAM Trần Thị Ngát1, 2*, Nguyễn Thị Phương Liên1, 2, Trương Xuân Lam1, 2 1Viện Sinh thái và Tài nguyên sinh vật, Viện Hàn lâm Khoa học và Công nghệ Việt Nam 2Học viện Khoa học và Công nghệ, Viện Hàn lâm Khoa học và Công nghệ Việt Nam *Email: [email protected] ĐẶT VẤN ĐỀ Liên họ Ong mật (Apoidea) là một trong những nhóm đa dạng và phong phú nhất trong Bộ Cánh màng. Cho đến nay, trên 20.000 loài thuộc 7 họ (Andrenidae, Apidae, Colletidae, Halictidae, Megachilidae, Melittidae và Stenotritidae) đã được mô tả trên thế giới (Ascher và Pickering, 2020). Ong mật được đánh giá là một trong những trợ thủ đắc lực cho quá trình thụ phấn cho các loài thực vật có hoa. Cụ thể, chúng tiến hành thụ phấn cho nhiều loại lương thực, thực phẩm thiết yếu cũng như các loại cây ăn quả quan trọng của nước ta như lúa, ngô, đậu, dưa, nhãn, vải hay bưởi,… Với khả năng thụ phấn tốt, chúng giúp năng suất cây trồng tăng lên 20-30 % so với thông thường, thậm chí là 50 % (Phạm Hồng Thái, 2014). Ngoài ra, một số các loài Ong mật đã được thuần nuôi và mang lại lợi ích kinh tế rất cao cho người nuôi ong bằng việc khai thác các sản phẩm được tạo ra bởi chúng như phấn hoa, sáp ong, sữa ong chúa, đặc biệt là mật ong. -
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. -
Iconic Bees: 12 Reports on UK Bee Species
Iconic Bees: 12 reports on UK bee species Bees are vital to the ecology of the UK and provide significant social and economic benefits through crop pollination and maintaining the character of the landscape. Recent years have seen substantial declines in many species of bees within the UK. This report takes a closer look at how 12 ‘iconic’ bee species are faring in each English region, as well as Wales, Northern Ireland and Scotland. Authors Rebecca L. Evans and Simon G. Potts, University of Reading. Photo: © Amelia Collins Contents 1 Summary 2 East England Sea-aster Mining Bee 6 East Midlands Large Garden Bumblebee 10 London Buff-tailed Bumblebee 14 North East Bilberry Bumblebee 18 North West Wall Mason Bee 22 Northern Ireland Northern Colletes 26 Scotland Great Yellow Bumblebee 30 South East England Potter Flower Bee 34 South West England Scabious Bee 38 Wales Large Mason Bee 42 West Midlands Long-horned Bee 46 Yorkshire Tormentil Mining Bee Through collating information on the 12 iconic bee species, common themes have Summary emerged on the causes of decline, and the actions that can be taken to help reverse it. The most pervasive causes of bee species decline are to be found in the way our countryside has changed in the past 60 years. Intensification of grazing regimes, an increase in pesticide use, loss of biodiverse field margins and hedgerows, the trend towards sterile monoculture, insensitive development and the sprawl of towns and cities are the main factors in this. I agree with the need for a comprehensive Bee Action Plan led by the UK Government in order to counteract these causes of decline, as called for by Friends of the Earth. -
Mitt IEV 2005 30 (1-2).Pdf
Band 30 Nr. 1-2 29. April 2005 MITTEILUNGEN DES INTERNATIONALEN ENTOMOLOGISCHEN VEREINS ISSN 1019-2808 Herausgeber Internationaler Entomologischer Verein e. V. gegr. 1884 Sitz: Frankfurt am Main. 1. Vorsitzender Dr. Thomas WAGNER, Universität Koblenz-Landau, Universi- tätsstraße 1, D-56070 Koblenz. E-Mail: [email protected] 2. Vorsitzender Dr. Horst BATHON, Biologische Bundesanstalt, Heinrichstraße 243, D-64287 Darmstadt. E-Mail: [email protected] Kassenwart Dr. Hannes GÜNTHER, Eisenacher Straße 25, D-55218 Ingel- heim. E-Mail: [email protected] Redaktion Dr. Michael GEISTHARDT, Auringer Straße 22, D-65207 Wies- baden. E-Mail: [email protected] Schriftführung Ute SCHNEIDER, Von-Krehl-Straße 7, D-65191 Wiesbaden. E-Mail: [email protected] Manuskripte Bitte „Richtlinien für die Annahme von Beiträgen“ beachten. Inhalt Die Autoren sind für den Inhalt ihrer Beiträge allein verantwort- lich; die Artikel geben nicht notwendigerweise die Meinung der Redaktion oder des Vereins wieder. Freiexemplare Die Autoren erhalten 50 Freiexemplare ihrer Artikel; werden weitere Exemplare zum Selbstkostenpreis gewünscht, so ist dies bei der Einsendung des Manuskripts zu vermerken. Abonnement Im Mitgliedsbeitrag enthalten, pro Jahr zur Zeit € 20,00, Schü- ler, Studenten und Auszubildende € 10,00 (Aufnahmegebühr € 3,00); für Nichtmitglieder € 24,50 zuzüglich Versandspesen. Einzelpreis Pro Einzelheft € 6,00; für Mitglieder € 2,50, zuzüglich Porto. Preise für Supplementbände nach Anfrage. Bestellungen an Ute SCHNEIDER oder Dr. M. GEISTHARDT. Konto 70721-600 (BLZ 50010060) bei der Postbank Frankfurt a. M. IBAN: DE55 5001 0060 0070 7216 00; BIC: PBNKDEFF Adressenänderungen an Ute SCHNEIDER oder Dr. Michael GEISTHARDT. Internet http://www.entomology-iev.de Copyright © 2005 by Internationaler entomologischer Verein. -
A Preliminary Detective Survey of Hymenopteran Insects at Jazan Lake Dam Region, Southwest of Saudi Arabia
Saudi Journal of Biological Sciences 28 (2021) 2342–2351 Contents lists available at ScienceDirect Saudi Journal of Biological Sciences journal homepage: www.sciencedirect.com Original article A preliminary detective survey of hymenopteran insects at Jazan Lake Dam Region, Southwest of Saudi Arabia Hanan Abo El-Kassem Bosly 1 Biology Department - Faculty of Science - Jazan University, Saudi Arabia article info abstract Article history: A preliminary detective survey for the hymenopteran insect fauna of Jazan Lake dam region, Southwest Received 16 November 2020 Saudi Arabia, was carried out for one year from January 2018 to January 2019 using mainly sweep nets Revised 6 January 2021 and Malaise traps. The survey revealed the presence of three hymenopteran Superfamilies (Apoidea, Accepted 12 January 2021 Vespoidea and Evanioidea) representing 15 species belonging to 10 genera of 6 families (Apidae, Available online 28 January 2021 Crabronidae, Sphecidae, Vespidae, Mutillidae, and Evaniidae). The largest number of species has belonged to the family Crabronidae is represented by 6 species under 2 genera. While the family Apidae, is repre- Keywords: sented by 2 species under 2 genera. Family Vespidae is represented by 2 species of one genus. While, the Survey rest of the families Sphecidae, Mutillida, and Evaniidae each is represented by only one species and one Insect fauna Hymenoptera genus each. Eleven species are predators, two species are pollinators and two species are parasitics. Note Jazan for each family was provided, and species was provided with synonyms and general and taxonomic Saudi Arabia remarks and their worldwide geographic distribution and information about their economic importance are also included. -
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. -
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.