The Story of Braula Coeca (Bee Lice) in Honeybee Colonies Apis Mellifera L. in Libya
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Torix Rickettsia Are Widespread in Arthropods and Reflect a Neglected Symbiosis
GigaScience, 10, 2021, 1–19 doi: 10.1093/gigascience/giab021 RESEARCH RESEARCH Torix Rickettsia are widespread in arthropods and Downloaded from https://academic.oup.com/gigascience/article/10/3/giab021/6187866 by guest on 05 August 2021 reflect a neglected symbiosis Jack Pilgrim 1,*, Panupong Thongprem 1, Helen R. Davison 1, Stefanos Siozios 1, Matthew Baylis1,2, Evgeny V. Zakharov3, Sujeevan Ratnasingham 3, Jeremy R. deWaard3, Craig R. Macadam4,M. Alex Smith5 and Gregory D. D. Hurst 1 1Institute of Infection, Veterinary and Ecological Sciences, Faculty of Health and Life Sciences, University of Liverpool, Leahurst Campus, Chester High Road, Neston, Wirral CH64 7TE, UK; 2Health Protection Research Unit in Emerging and Zoonotic Infections, University of Liverpool, 8 West Derby Street, Liverpool L69 7BE, UK; 3Centre for Biodiversity Genomics, University of Guelph, 50 Stone Road East, Guelph, Ontario N1G2W1, Canada; 4Buglife – The Invertebrate Conservation Trust, Balallan House, 24 Allan Park, Stirling FK8 2QG, UK and 5Department of Integrative Biology, University of Guelph, Summerlee Science Complex, Guelph, Ontario N1G 2W1, Canada ∗Correspondence address. Jack Pilgrim, Institute of Infection, Veterinary and Ecological Sciences, Faculty of Health and Life Sciences, University of Liverpool, Liverpool, UK. E-mail: [email protected] http://orcid.org/0000-0002-2941-1482 Abstract Background: Rickettsia are intracellular bacteria best known as the causative agents of human and animal diseases. Although these medically important Rickettsia are often transmitted via haematophagous arthropods, other Rickettsia, such as those in the Torix group, appear to reside exclusively in invertebrates and protists with no secondary vertebrate host. Importantly, little is known about the diversity or host range of Torix group Rickettsia. -
Friedrich Ruttner Biogeography and Taxonomy of Honeybees
Friedrich Ruttner Biogeography and Taxonomy of Honeybees With 161 Figures Springer-Verlag Berlin Heidelberg GmbH Professor Dr. FRIEDRICH RUTTNER Bodingbachstraße 16 A-3293 Lunz am See Legend for cover mOlif: Four species of honeybees around the area of distribution. ISBN 978-3-642-72651-4 ISBN 978-3-642-72649-1 (eBook) DOI 10.1007/978-3-642-72649-1 Library of Congress Cataloging in Publication Data. Ruttner, Friedrich. Biogeogra phy and taxonomy of honeybees/Friedrich Ruttner. p. cm. Bibliography: p. In c\udes. index. 1. Apis (Insects) 2. Honeybee. I. TitIe. QL568.A6R88 1987 595.79'9--dc19 This work is subject to copyright. All rights are reserved, whether the whole or part of the material is concerned, specifically the rights of translation, reprinting, re-use of illustrations, recitation, broadcasting, reproduction on microfilms or in other ways, and storage in data banks. Duplication of this publication or parts thereof is only permitted under the provisions of the German Copyright Law of September 9, 1965, in its version of lune 24, 1985, and a copyright fee must always be paid. Vio lations fall under the prosecution act of the German Copyright Law. © Springer-Verlag Berlin Heidelberg 1988 Originally published by Springer-Verlag Berlin Heidelberg New York in 1988 Softcover reprint of the hardcover 18t edition 1988 The use of registered names, trademarks, etc. in this publication does not imply, even in th absence of a specific statement, that such names are exempt from the relevant prutective laws and regulations and therefore free for general use. Data conversion and bookbinding: Appl, Wemding. -
Folk Taxonomy, Nomenclature, Medicinal and Other Uses, Folklore, and Nature Conservation Viktor Ulicsni1* , Ingvar Svanberg2 and Zsolt Molnár3
Ulicsni et al. Journal of Ethnobiology and Ethnomedicine (2016) 12:47 DOI 10.1186/s13002-016-0118-7 RESEARCH Open Access Folk knowledge of invertebrates in Central Europe - folk taxonomy, nomenclature, medicinal and other uses, folklore, and nature conservation Viktor Ulicsni1* , Ingvar Svanberg2 and Zsolt Molnár3 Abstract Background: There is scarce information about European folk knowledge of wild invertebrate fauna. We have documented such folk knowledge in three regions, in Romania, Slovakia and Croatia. We provide a list of folk taxa, and discuss folk biological classification and nomenclature, salient features, uses, related proverbs and sayings, and conservation. Methods: We collected data among Hungarian-speaking people practising small-scale, traditional agriculture. We studied “all” invertebrate species (species groups) potentially occurring in the vicinity of the settlements. We used photos, held semi-structured interviews, and conducted picture sorting. Results: We documented 208 invertebrate folk taxa. Many species were known which have, to our knowledge, no economic significance. 36 % of the species were known to at least half of the informants. Knowledge reliability was high, although informants were sometimes prone to exaggeration. 93 % of folk taxa had their own individual names, and 90 % of the taxa were embedded in the folk taxonomy. Twenty four species were of direct use to humans (4 medicinal, 5 consumed, 11 as bait, 2 as playthings). Completely new was the discovery that the honey stomachs of black-coloured carpenter bees (Xylocopa violacea, X. valga)were consumed. 30 taxa were associated with a proverb or used for weather forecasting, or predicting harvests. Conscious ideas about conserving invertebrates only occurred with a few taxa, but informants would generally refrain from harming firebugs (Pyrrhocoris apterus), field crickets (Gryllus campestris) and most butterflies. -
Of the Vitosha Mountain
Historia naturalis bulgarica 26: 1–66 ISSN 0205-3640 (print) | ISSN 2603-3186 (online) • http://www.nmnhs.com/historia-naturalis-bulgarica/ publication date [online]: 17 May 2018 The Dipterans (Insecta: Diptera) of the Vitosha Mountain Zdravko Hubenov Abstract. A total of 1272 two-winged species that belong to 58 families has been reported from theVitosha Mt. The Tachinidae (208 species or 16.3%) and Cecidomyiidae (138 species or 10.8%) are the most numerous. The greatest number of species has been found in the mesophylic and xeromesophylic mixed forests belt (707 species or 55.6%) and in the northern part of the mountain (645 species or 50.7%). The established species belong to 83 areographical categories. The dipterous fauna can be divided into two main groups: 1) species with Mediterranean type of distribution (53 species or 4.2%) – more thermophilic and distributed mainly in the southern parts of the Palaearctic; seven species of southern type, distributed in the Palaearctic and beyond it, can be formally related to this group as well; 2) species with Palaearctic and Eurosiberian type of distribution (1219 species or 95.8%) – more cold-resistant and widely distributed in the Palaearctic; 247 species of northern type, distributed in the Palaearctic and beyond it, can be formally related to this group as well. The endemic species are 15 (1.2%). The distribution of the species according to the zoogeographical categories in the vegetation belts and the distribution of the zoogeographical categories in each belt are considered. The dipteran fauna of the Vitosha Mt. is compared to this of the Rila and Pirin Mountains. -
Episodic Radiations in the Fly Tree of Life
Episodic radiations in the fly tree of life Brian M. Wiegmanna,1, Michelle D. Trautweina, Isaac S. Winklera, Norman B. Barra,b, Jung-Wook Kima, Christine Lambkinc,d, Matthew A. Bertonea, Brian K. Cassela, Keith M. Baylessa, Alysha M. Heimberge, Benjamin M. Wheelerf, Kevin J. Petersone, Thomas Papeg, Bradley J. Sinclairh, Jeffrey H. Skevingtoni, Vladimir Blagoderovj, Jason Caravask, Sujatha Narayanan Kuttyl, Urs Schmidt-Ottm, Gail E. Kampmeiern, F. Christian Thompsono, David A. Grimaldip, Andrew T. Beckenbachq, Gregory W. Courtneyr, Markus Friedrichk, Rudolf Meierl,s, and David K. Yeatesd Departments of aEntomology and fComputer Science, North Carolina State University, Raleigh, NC 27695; bCenter for Plant Health Science and Technology, Mission Laboratory, US Department of Agriculture-Animal and Plant Health Inspection Service, Moore Air Base, Edinburg, TX 78541; cQueensland Museum, South Bank, Brisbane, Queensland 4101, Australia; eDepartment of Biological Sciences, Dartmouth College, Hanover, NH 03755; gNatural History Museum of Denmark, University of Copenhagen, 2100 Copenhagen Ø, Denmark; hCanadian National Collection of Insects, Ottawa Plant Laboratory-Entomology, Canadian Food Inspection Agency, Ottawa, ON, Canada K1A 0C6; iInvertebrate Biodiversity, Agriculture and Agri-Food Canada, Ottawa, ON, Canada K1A 0C6; jDepartment of Entomology, Natural History Museum, London SW7 5BD, United Kingdom; kDepartment of Biological Sciences, Wayne State University, Detroit, MI 48202; lDepartment of Biological Sciences and sUniversity Scholars Programme, -
Encyclopedia of Social Insects
G Guests of Social Insects resources and homeostatic conditions. At the same time, successful adaptation to the inner envi- Thomas Parmentier ronment shields them from many predators that Terrestrial Ecology Unit (TEREC), Department of cannot penetrate this hostile space. Social insect Biology, Ghent University, Ghent, Belgium associates are generally known as their guests Laboratory of Socioecology and Socioevolution, or inquilines (Lat. inquilinus: tenant, lodger). KU Leuven, Leuven, Belgium Most such guests live permanently in the host’s Research Unit of Environmental and nest, while some also spend a part of their life Evolutionary Biology, Namur Institute of cycle outside of it. Guests are typically arthropods Complex Systems, and Institute of Life, Earth, associated with one of the four groups of eusocial and the Environment, University of Namur, insects. They are referred to as myrmecophiles Namur, Belgium or ant guests, termitophiles, melittophiles or bee guests, and sphecophiles or wasp guests. The term “myrmecophile” can also be used in a broad sense Synonyms to characterize any organism that depends on ants, including some bacteria, fungi, plants, aphids, Inquilines; Myrmecophiles; Nest parasites; and even birds. It is used here in the narrow Symbionts; Termitophiles sense of arthropods that associated closely with ant nests. Social insect nests may also be parasit- Social insect nests provide a rich microhabitat, ized by other social insects, commonly known as often lavishly endowed with long-lasting social parasites. Although some strategies (mainly resources, such as brood, retrieved or cultivated chemical deception) are similar, the guests of food, and nutrient-rich refuse. Moreover, nest social insects and social parasites greatly differ temperature and humidity are often strictly regu- in terms of their biology, host interaction, host lated. -
Insect Egg Size and Shape Evolve with Ecology but Not Developmental Rate Samuel H
ARTICLE https://doi.org/10.1038/s41586-019-1302-4 Insect egg size and shape evolve with ecology but not developmental rate Samuel H. Church1,4*, Seth Donoughe1,3,4, Bruno A. S. de Medeiros1 & Cassandra G. Extavour1,2* Over the course of evolution, organism size has diversified markedly. Changes in size are thought to have occurred because of developmental, morphological and/or ecological pressures. To perform phylogenetic tests of the potential effects of these pressures, here we generated a dataset of more than ten thousand descriptions of insect eggs, and combined these with genetic and life-history datasets. We show that, across eight orders of magnitude of variation in egg volume, the relationship between size and shape itself evolves, such that previously predicted global patterns of scaling do not adequately explain the diversity in egg shapes. We show that egg size is not correlated with developmental rate and that, for many insects, egg size is not correlated with adult body size. Instead, we find that the evolution of parasitoidism and aquatic oviposition help to explain the diversification in the size and shape of insect eggs. Our study suggests that where eggs are laid, rather than universal allometric constants, underlies the evolution of insect egg size and shape. Size is a fundamental factor in many biological processes. The size of an 526 families and every currently described extant hexapod order24 organism may affect interactions both with other organisms and with (Fig. 1a and Supplementary Fig. 1). We combined this dataset with the environment1,2, it scales with features of morphology and physi- backbone hexapod phylogenies25,26 that we enriched to include taxa ology3, and larger animals often have higher fitness4. -
Prevalence of Bee Lice Braula Coeca (Diptera: Braulidae) and Other Perceived Constraints to Honey Bee Production in Wukro Woreda, Tigray Region, Ethiopia
Global Veterinaria 8 (6): 631-635, 2012 ISSN 1992-6197 © IDOSI Publications, 2012 Prevalence of Bee Lice Braula coeca (Diptera: Braulidae) and Other Perceived Constraints to Honey Bee Production in Wukro Woreda, Tigray Region, Ethiopia 12Adeday Gidey, Shiferaw Mulugeta and 2Abebe Fromsa 1Tigray Region, Bureau of Agriculture, Ethiopia 2College of Agriculture and Veterinary Medicine, Jimma University, P.O. Box: 307, Jimma, Ethiopia Abstract: A cross sectional study was conducted from November 2008 to March 2009 in Wukro Woreda to determine the prevalence of bee lice and other constraints to honey bee production in the area. The result revealed an overall Braula coeca (bee louse) prevalence of 4% in the brood and 5.5% in the adult honey bees, respectively. The prevalence of louse infestation recorded in brood and adult bee of the three peasant associations of Wukro Woreda were, 3.3%, 5% in Genfel, 4.9%, 6% in Adikisandid and 3%, 5%, Aynalem, respectively. There was no statistically significant variation in overall prevalence rates of lice infestation between brood and adult bees and locations (P> 0.05). Factors perceived as major constraints to honeybee production by 51 interviewed farmers were frequent occurrence of drought, lack of bee forage, existence of pests and predators and pesticide poisoning in decreasing order of importance. The beekeepers also listed pests and predators that they considered important to be honey badgers, ant like insects, wax moth, birds, spiders, monkeys, snakes and lizards. According to the response of beekeepers, honey badger attack was a serious problem in the Woreda. This study revealed the presence of real threat to beekeeping and honey production from louse infestation, predators, chemical pollution and drought. -
F. Christian Thompson Neal L. Evenhuis and Curtis W. Sabrosky Bibliography of the Family-Group Names of Diptera
F. Christian Thompson Neal L. Evenhuis and Curtis W. Sabrosky Bibliography of the Family-Group Names of Diptera Bibliography Thompson, F. C, Evenhuis, N. L. & Sabrosky, C. W. The following bibliography gives full references to 2,982 works cited in the catalog as well as additional ones cited within the bibliography. A concerted effort was made to examine as many of the cited references as possible in order to ensure accurate citation of authorship, date, title, and pagination. References are listed alphabetically by author and chronologically for multiple articles with the same authorship. In cases where more than one article was published by an author(s) in a particular year, a suffix letter follows the year (letters are listed alphabetically according to publication chronology). Authors' names: Names of authors are cited in the bibliography the same as they are in the text for proper association of literature citations with entries in the catalog. Because of the differing treatments of names, especially those containing articles such as "de," "del," "van," "Le," etc., these names are cross-indexed in the bibliography under the various ways in which they may be treated elsewhere. For Russian and other names in Cyrillic and other non-Latin character sets, we follow the spelling used by the authors themselves. Dates of publication: Dating of these works was obtained through various methods in order to obtain as accurate a date of publication as possible for purposes of priority in nomenclature. Dates found in the original works or by outside evidence are placed in brackets after the literature citation. -
Honeybee Health in Africa – a Review
Honeybee health in Africa – a review Christian, W.W. Pirk, Ursula Strauss, Abdullahi, A. Yusuf, Fabien Démares and Hannelie Human* Social Insects Research Group, Department of Zoology and Entomology, University of Pretoria, Private Bag X20, Hatfield, 0028 Pretoria, South Africa *Corresponding author email: [email protected] Abstract Honeybee (Apis mellifera L.) pathogens and parasites and the negative effects thereof on honeybee populations remain an issue of public concern and the subject of active research. Africa with its high genetic diversity of honeybee sub-species and the large wild population is also exposed to the various factors responsible for colony losses in other parts of the world. Apart from the current American foulbrood epidemic in the Western Cape of South Africa, no large scale colony losses have been reported elsewhere on the continent. We discuss the presence of pathogens, parasites, pests and predators of African honeybees as well as the threats they face in relation to habitat changes arising from the impact of increased human populations. In addition, we discuss current efforts aimed at protecting and promoting the health of African honeybees. Keywords: honeybees/ Africa/ honeybee health/ pathogens/ parasites/ pests/ predators/ habitat loss 1 1. INTRODUCTION The crucial service and economic value of the majority of Apis and non-Apis pollinators have been reviewed and debated extensively (Aebi et al. 2012; Ollerton et al. 2012; Vanbergen et al. 2013). Honeybees (Apis mellifera L.), both wild and managed, are responsible for the pollination of numerous crops and plants, contributing not only to food security but also the economy (Klein et al. -
ABSTRACT BAYLESS, KEITH MOHR. Phylogenomic Studies of Evolutionary Radiations of Diptera
ABSTRACT BAYLESS, KEITH MOHR. Phylogenomic Studies of Evolutionary Radiations of Diptera. (Under the direction of Dr. Brian M. Wiegmann.) Efforts to understand the evolutionary history of flies have been obstructed by the lack of resolution in major radiations. Diptera is a highly diverse branch on the tree of life, but this diversity accrued at an uneven pace. Some of radiations that contributed disproportionately to species diversity occurred contemporaneously, and understanding the relationships of these taxa can illuminate broad scale patterns. Relationships between some subordinate groups of taxa are notoriously difficult to untangle, and genomic data will address these problems at a new scale. This project will focus on two major radiations in Diptera: Tabanus horse flies and relatives, and acalyptrate Schizophora. Tabanus includes over one thousand species. Synthesis focused research on the group is stymied by its species richness, worldwide distribution, inconsistent diagnosis, and scale of undescribed diversity. Furthermore, the genus may be non-monophyletic with respect to more than 10 other lineages of horse flies. A groundwork phylogenetic study of worldwide Tabanus is needed to understand the evolution of this lineage and to make comprehensive taxonomic projects manageable. Data to address this question was collected from two different sources. A dataset including five genes was sequenced from ninety-four species in the Tabanus group, including nearly all genera of Tabanini and at least one species from every biogeographic region. Then a new data source from a next generation sequencing approach, Anchored Hybrid Enrichment exome capture, was used to accumulate a dataset including hundreds of genes for a subset of the taxa. -
Biosecurity Or Disease Risk Mitigation Strategy for the Australian Honey Bee Industry
BIOSECURITY OR DISEASE RISK MITIGATION STRATEGY FOR THE AUSTRALIAN HONEY BEE INDUSTRY Australian Honey Bee Industry Council Postal Address: PO Box R838 ROYAL EXCHANGE NSW 1225 Phone: 61 2 9221 0911\ Fax: 61 2 9221 p922 Email: [email protected] Web: www.honeybee.org.au Australian Honey bee Industry Biosecurity Plan TABLE OF CONTENTS Page Introduction 2 The Honey Bee Industry Biosecurity Plan 2 Main Diseases or Pests A. Endemic Diseases or Pests 3 1) American foulbrood 2) European foulbrood. B. Exotic Diseases or Pests 3 1) Tropilaelaps mite 2) Varroa mite (destructor) 3) Varroa mite (jacobsoni) 4) Braula fly 5) Tracheal mite 6) Asian bees 7) Africanised and Cape Honey Bees 8) Small Hive Beetle General Awareness of Disease 6 Introduction of Disease 7 Spread within the Apiary 8 Spread to other Apiaries 8 Integration of Biosecurity 9 1 Australian Honey bee Industry Biosecurity Plan BIOSECURITY OR DISEASE RISK MITIGATION STRATEGY FOR THE AUSTRALIAN HONEY BEE INDUSTRY Introduction In a broad sense, biosecurity is a set of measures designed to protect an animal population from transmissible infectious agents at a national, regional and individual farm level. They are designed with the emphasis on managing risk without affecting profitability through excessively strict precautions. At the farm level it involves a systematic approach of producers on an industry wide basis in providing protection against the entry and spread of disease and parasites. Poor biosecurity will contribute to the likelihood of the occurrence and severity of a disease outbreak and may burden governments and industries with unnecessary costs. Biosecurity for the honey bee industry is therefore about managing risk to prevent the introduction of diseases to an apiary and to prevent the spread of diseases between apiaries or to a disease free area.