Management of Beneficial Insects 2 (1+1) B.Sc
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Conservation of Asian Honey Bees Benjamin P
Conservation of Asian honey bees Benjamin P. Oldroyd, Piyamas Nanork To cite this version: Benjamin P. Oldroyd, Piyamas Nanork. Conservation of Asian honey bees. Apidologie, Springer Verlag, 2009, 40 (3), 10.1051/apido/2009021. hal-00892024 HAL Id: hal-00892024 https://hal.archives-ouvertes.fr/hal-00892024 Submitted on 1 Jan 2009 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 40 (2009) 296–312 Available online at: c INRA/DIB-AGIB/EDP Sciences, 2009 www.apidologie.org DOI: 10.1051/apido/2009021 Review article Conservation of Asian honey bees* Benjamin P. Oldroyd1, Piyamas Nanork2 1 Behaviour and Genetics of Social Insects Lab, School of Biological Sciences A12, University of Sydney, NSW 2006, Australia 2 Department of Biology, Mahasarakham University, Mahasarakham, Thailand Received 26 June 2008 – Revised 14 October 2008 – Accepted 29 October 2008 Abstract – East Asia is home to at least 9 indigenous species of honey bee. These bees are extremely valu- able because they are key pollinators of about 1/3 of crop species, provide significant income to some of the world’s poorest people, and are prey items for some endemic vertebrates. -
Ecology, Behaviour and Control of Apis Cerana with a Focus on Relevance to the Australian Incursion
Insects 2013, 4, 558-592; doi:10.3390/insects4040558 OPEN ACCESS insects ISSN 2075-4450 www.mdpi.com/journal/insects/ Review Ecology, Behaviour and Control of Apis cerana with a Focus on Relevance to the Australian Incursion Anna H. Koetz Biosecurity Queensland, Department of Agriculture, Fisheries and Forestry, 21-23 Redden St., Portsmith, QLD 4870, Australia; E-Mail: [email protected]; Tel.: +61-419-726-698; Fax: +61-7-4057-3690 Received: 27 June 2013; in revised form: 13 September 2013 / Accepted: 24 September 2013 / Published: 21 October 2013 Abstract: Apis cerana Fabricius is endemic to most of Asia, where it has been used for honey production and pollination services for thousands of years. Since the 1980s, A. cerana has been introduced to areas outside its natural range (namely New Guinea, the Solomon Islands, and Australia), which sparked fears that it may become a pest species that could compete with, and negatively affect, native Australian fauna and flora, as well as commercially kept A. mellifera and commercial crops. This literature review is a response to these concerns and reviews what is known about the ecology and behaviour of A. cerana. Differences between temperate and tropical strains of A. cerana are reviewed, as are A. cerana pollination, competition between A. cerana and A. mellifera, and the impact and control strategies of introduced A. cerana, with a particular focus on gaps of current knowledge. Keywords: Apis cerana; Apis mellifera; incursion; pest species; Australia; pollination; competition; distribution; control 1. Introduction Apis cerana Fabricius (also known as the Asian honeybee, Asiatic bee, Asian hive bee, Indian honeybee, Indian bee, Chinese bee, Mee bee, Eastern honeybee, and Fly Bee) is endemic to most of Asia where it has been used for honey production and pollination services for thousands of years. -
Aggregations of Unrelated Apis Florea Colonies Wandee Wattanachaiyingcharoen, Siriwat Wongsiri, Benjamin P
Aggregations of unrelated Apis florea colonies Wandee Wattanachaiyingcharoen, Siriwat Wongsiri, Benjamin P. Oldroyd To cite this version: Wandee Wattanachaiyingcharoen, Siriwat Wongsiri, Benjamin P. Oldroyd. Aggregations of unrelated Apis florea colonies. Apidologie, Springer Verlag, 2008, 39 (5), pp.531-536. hal-00891920 HAL Id: hal-00891920 https://hal.archives-ouvertes.fr/hal-00891920 Submitted on 1 Jan 2008 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 39 (2008) 531–536 Available online at: c INRA/DIB-AGIB/ EDP Sciences, 2008 www.apidologie.org DOI: 10.1051/apido:2008045 Original article Aggregations of unrelated Apis florea colonies* Wandee Wattanachaiyingcharoen1, Siriwat Wongsiri2,BenjaminP.Oldroyd3 1 Department of Biology, Faculty of Science, Naresuan University, Phitsanulok 65000, Thailand 2 Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok 10320, Thailand 3 Behaviour and Genetics of Social Insects Lab, School of Biological Sciences A12, University of Sydney, NSW 2006, Australia Received 5 July 2007 – Revised 25 March 2008 – Accepted 13 May 2008 Abstract – Intensive surveys of an area of woodland in Phitsanulok province, Thailand, revealed 15 colonies of Apis florea. The colonies had a highly aggregated spatial distribution (Standardized Morisita’s Index of Dispersion = 0.59). -
Bee Viruses: Routes of Infection in Hymenoptera
fmicb-11-00943 May 27, 2020 Time: 14:39 # 1 REVIEW published: 28 May 2020 doi: 10.3389/fmicb.2020.00943 Bee Viruses: Routes of Infection in Hymenoptera Orlando Yañez1,2*, Niels Piot3, Anne Dalmon4, Joachim R. de Miranda5, Panuwan Chantawannakul6,7, Delphine Panziera8,9, Esmaeil Amiri10,11, Guy Smagghe3, Declan Schroeder12,13 and Nor Chejanovsky14* 1 Institute of Bee Health, Vetsuisse Faculty, University of Bern, Bern, Switzerland, 2 Agroscope, Swiss Bee Research Centre, Bern, Switzerland, 3 Laboratory of Agrozoology, Department of Plants and Crops, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium, 4 INRAE, Unité de Recherche Abeilles et Environnement, Avignon, France, 5 Department of Ecology, Swedish University of Agricultural Sciences, Uppsala, Sweden, 6 Environmental Science Research Center, Faculty of Science, Chiang Mai University, Chiang Mai, Thailand, 7 Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai, Thailand, 8 General Zoology, Institute for Biology, Martin-Luther-University of Halle-Wittenberg, Halle (Saale), Germany, 9 Halle-Jena-Leipzig, German Centre for Integrative Biodiversity Research (iDiv), Leipzig, Germany, 10 Department of Biology, University of North Carolina at Greensboro, Greensboro, NC, United States, 11 Department Edited by: of Entomology and Plant Pathology, North Carolina State University, Raleigh, NC, United States, 12 Department of Veterinary Akio Adachi, Population Medicine, College of Veterinary Medicine, University of Minnesota, Saint Paul, MN, United States, -
Cambodian Cashew Industry
Nominating the bee trees of Nandagudi/Ramagovindapura as a World’s First Bee Heritage Site Presented by: Stephen PETERSEN Apicultural Consultant, Toklat Apiaries Fairbanks, Alaska, USA And Muniswamyreddy Shankar REDDY Centre for Apicultural Studies, Department of Zoology, Bangalore University, Jnana Bharathi, Bangalore-560056, INDIA Honeybee species found in SE Asia Apis dorsata, Thailand Apis florea, India Apis cerana, Philippines Single comb, exposed nests Multi comb, enclosed nests Giant Honeybees Cavity nesting bees Apis dorsata (3 sub-species) Apis cerana (6 sub-species) i. Apis dorsata dorsata (1) Apis cerana koschevnikovi ii. Apis dorsata binghami (2) Apis cerana nigrocincta iii. Apis dorsata breviligula (3) Apis cerana nuluensis Apis laboriosa (4) Apis cerana cerana Dwarf or Small Honeybees (5) Apis cerana indica Apis andreniformis (6) Apis cerana himalaya Apis florea Introduced species Apis mellifera Distribution of Apis dorsata sub-species in Asia. Apis dorsata Bangalore breviligula Apis dorsata dorsata Apis dorsata binghami © Stephen Petersen - Apicultural Consultant Apis dorsata – are most typically found in aggregated nesting sites in emergent trees © Stephen Petersen - Apicultural Consultant They frequently nest on man-made structures; apartment buildings, bill boards and water towers are favorites at Bangalore Bill board, Airport Road Water tank, ITI Water Tank, Air Force Station The village of Ramagovindapura; a unique aggregation of Apis dorsata colonies. In January, 2010 there were at least 630 colonies nesting in one tree in the center of Ramagovindapura village © M.S. Reddy Colonies monitored in Ramagovindapura tree Number of Number of Income Year Apis dorsata colonies Remarks generation bee colonies harvested 1998 252 70 Rs. 12,000=00 1999 310 110 Rs. -
Species from Sympatric Apis Florea (Fabricius, 1787)
Original article Evidence of reproductive isolation confirms that Apis andreniformis (Smith, 1858) is a separate species from sympatric Apis florea (Fabricius, 1787) S Wongsiri K Limbipichai P Tangkanasing M Mardan T Rinderer HA Sylvester G Koeniger G Otis 1 Bee Biology Research Unit, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand; 2 Department of Plant Protection, Universiti Pertanian Malaysia, 43400 Serdang, Selangor, Malaysia; 3 Honey-Bee Breeding, Genetics & Physiology Research 1157 Ben Hur Road, Baton Rouge, Louisiana 70820, USA; 4 Institut für Bienenkunde D 6370 Oberursel 1, FRG (Received 7 September 1989; accepted 29 September 1989) Summary — The species Apis andreniformis (Smith, 1858), the small dwarf honey bee of South- east Asia, is recognized as a valid biological species. This recognition is based on distinctive endo- phallus characteristics in comparison with sympatric Apis florea (Fabricius, 1787). Additionally, scan- ning electron microscope images of drone basitarsi are presented, as are preliminary comparisons of wing venation. Apis florea / Apis andreniformis / taxonomy / reproductive isolation INTRODUCTION characteristics of Apis florea (Fabricius, 1787) that are reported for worker bees (Maa, 1953). In 1984, our group collected dwarf honey bees in Thailand in the province of Chan- Wu and Kuang (1986, 1987) reported taburi near the border with Kampuchea. that secondary sex characteristics differed Laboratory examinations of worker bees between drones of A florea and A andre- from these collections revealed that some formis. Specifically, both have a furcated bees had the species specific characteris- basitarsus, presumably modified to grasp tics of Apis andreniformis (Smith, 1858) queens during mating (see Ruttner, 1988). and that others had the species specific The furcated basitarsus is quite different in * Correspondence and reprints. -
Apis Cerana, Has Lower Antennal Sensitivity and Decreased
www.nature.com/scientificreports OPEN Resisting majesty: Apis cerana, has lower antennal sensitivity and decreased attraction to queen Received: 24 August 2016 Accepted: 13 February 2017 mandibular pheromone than Apis Published: 15 March 2017 mellifera Shihao Dong1,2,*, Ping Wen1,*, Qi Zhang2, Xinyu Li2, Ken Tan1,2 & James Nieh3 In highly social bees, queen mandibular pheromone (QMP) is vital for colony life. Both Apis cerana (Ac) and Apis mellifera (Am) share an evolutionarily conserved set of QMP compounds: (E)-9-oxodec- 2-enoic acid (9-ODA), (E)-9-hydroxydec-2-enoic acid (9-HDA), (E)-10-hydroxy-dec-2-enoic acid (10- HDA), 10-hydroxy-decanoic acid (10-HDAA), and methyl p–hydroxybenzoate (HOB) found at similar levels. However, evidence suggests there may be species-specific sensitivity differences to QMP compounds because Ac workers have higher levels of ovarian activation than Am workers. Using electroantennograms, we found species-specific sensitivity differences for a blend of the major QMP compounds and three individual compounds (9-HDA, 10-HDAA, and 10-HDA). As predicted, Am was more sensitive than Ac in all cases (1.3- to 2.7- fold higher responses). There were also species differences in worker retinue attraction to three compounds (9-HDA, HOB, and 10-HDA). In all significantly different cases,Am workers were 4.5- to 6.2-fold more strongly attracted than Ac workers were. Thus, Ac workers responded less strongly to QMP than Am workers, and 9-HDA and 10-HDA consistently elicited stronger antennal and retinue formation responses. Honey bee queens produce a pheromone, queen mandibular pheromone (QMP), which plays a central role in colony life and has multiple effects, depending upon the receivers and the context1–3. -
How Can Honey Bees Explain the Process of Animal Domestication by Humans?
Arthropods, 2020, 9(2): 32-37 Article How can honey bees explain the process of animal domestication by humans? Hossam F. Abou-Shaara Department of Plant Protection, Faculty of Agriculture, Damanhour University, Damanhour 22516, Egypt E-mail: [email protected] Received 1 February 2020; Accepted 5 March 2020 ; Published 1 June 2020 Abstract Animal domestication depends on complex relationships between humans and animals. There are many questions related to the domestication still incompletely solved especially since animal domestication occurred at specific regions in the past, and the percentage of domesticated animals is low. It is not easy to change characteristics and behaviors of wild animals, and humans can only train them to do specific tasks in most cases. Some species of honey bees, genus Apis, are wild and others are domesticated. In this article, domestication steps of honey bees by humans was used as a model to explain the early domestication process for other animals and to present answers to unsolved questions. Keywords beekeeping; selection; characteristics; history. Arthropods ISSN 22244255 URL: http://www.iaees.org/publications/journals/arthropods/onlineversion.asp RSS: http://www.iaees.org/publications/journals/arthropods/rss.xml Email: [email protected] EditorinChief: WenJun Zhang Publisher: International Academy of Ecology and Environmental Sciences 1 Introduction Some animals can simply be kept by humans and some of them can serve humans, for example donkeys. Donkeys for a long period of time were the main transportation means and they can be easily kept by humans in closed and open environments. Horses are another example, and the hybridization between horses and donkeys gives domesticated hybrids which can also be kept by humans. -
Genes Involved in Convergent Evolution of Eusociality in Bees
Genes involved in convergent evolution of eusociality in bees S. Hollis Woodarda,1, Brielle J. Fischmana,1, Aarti Venkatb, Matt E. Hudsonb, Kranthi Varalab, Sydney A. Cameronc, Andrew G. Clarkd, and Gene E. Robinsona,c,e,f,2 aProgram in Ecology, Evolution, and Conservation Biology, Departments of bCrop Sciences and cEntomology, eInstitute for Genomic Biology, and fNeuroscience Program, University of Illinois, Urbana, IL 61801; and dDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853 Contributed by Gene E. Robinson, March 12, 2011 (sent for review February 17, 2011) Eusociality has arisen independently at least 11 times in insects. different social lifestyles among relatively closely related species. Despite this convergence, there are striking differences among Furthermore, the extensive knowledge of bee natural history (8, eusocial lifestyles, ranging from species living in small colonies 13, 14) provides a valuable framework for developing hypotheses with overt conflict over reproduction to species in which colonies about the adaptive significance of genetic changes detected in contain hundreds of thousands of highly specialized sterile work- eusocial bee lineages. ers produced by one or a few queens. Although the evolution of To study patterns of molecular evolution associated with eusociality has been intensively studied, the genetic changes eusociality in bees, we generated ~1 Gbp of expressed sequence involved in the evolution of eusociality are relatively unknown. tags (ESTs) from a set of nine bee species (Table S1). This set of We examined patterns of molecular evolution across three in- species reflects the remarkable social diversity in bees by in- dependent origins of eusociality by sequencing transcriptomes of cluding eusocial and non-eusocial species; three origins of euso- nine socially diverse bee species and combining these data with ciality (9, 10); and two different forms of eusocial lifestyle, “highly genome sequence from the honey bee Apis mellifera to generate eusocial” and “primitively eusocial” (ref. -
Parasites, Pathogens, and Pests of Honeybees in Asia Panuwan Chantawannakul, Lilia I
Parasites, pathogens, and pests of honeybees in Asia Panuwan Chantawannakul, Lilia I. de Guzman, Jilian Li, Geoffrey R. Williams To cite this version: Panuwan Chantawannakul, Lilia I. de Guzman, Jilian Li, Geoffrey R. Williams. Parasites, pathogens, and pests of honeybees in Asia. Apidologie, Springer Verlag, 2016, 47 (3), pp.301-324. 10.1007/s13592-015-0407-5. hal-01532338 HAL Id: hal-01532338 https://hal.archives-ouvertes.fr/hal-01532338 Submitted on 2 Jun 2017 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 (2016) 47:301–324 Review article * INRA, DIB and Springer-Verlag France, 2015 DOI: 10.1007/s13592-015-0407-5 Parasites, pathogens, and pests of honeybees in Asia 1 2 3 4,5 Panuwan CHANTAWANNAKUL , Lilia I. de GUZMAN , Jilian LI , Geoffrey R. WILLIAMS 1Bee Protection Laboratory (BeeP), Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand 2Honey Bee Breeding, Genetics and Physiology Laboratory, USDA-ARS, Baton Rouge, LA 70820, USA 3Key Laboratory of Pollinating Insect Biology of the Ministry of Agriculture, Institute of Apicultural Research, Chinese Academy of Agricultural Sciences, Beijing 100093, China 4Institute of Bee Health, Vetsuisse Faculty, University of Bern, 3003, Bern, Switzerland 5Agroscope, Swiss Bee Research Centre, 3003, Bern, Switzerland Received 20 May 2015 – Revised 7 October 2015 – Accepted 26 October 2015 Abstract – Asia is home to at least nine honeybee species, including the introduced Apis mellifera .Inadditionto A. -
Of Apis Cerana Indica in Comparison to Apis Mellifera Ligustica
Original article Juvenile hormone titer and reproduction of Varroa jacobsoni in capped brood stages of Apis cerana indica in comparison to Apis mellifera ligustica P Rosenkranz NC Tewarson A Rachinsky A Strambi C Strambi W Engels 1 LS Entwicklungsphysiologie, Zoologisches Institut der Universität, Auf der Morgenstelle 28, D-72076 Tübingen, Germany; 2 Department of Zoology, Ewing Christian College, Allahabad-211003, India; 3 Laboratoire de Neurobiologie, CNHS, BP 71, F-13402 Marseille Cedex 9, France (Received 24 November 1992; accepted 19 February 1993) Summary — The juvenile hormone (JH) III hemolymph titer of late larval and early pupal stages as determined by radioimmunoassay (RIA) does not differ significantly in Apis cerana and Apis mellife- ra, particularly in freshly-sealed worker brood. In drone brood, slightly higher JH III hemolymph con- centrations were recorded. These results do not agree with the hypothesis that reproduction of the parasitic bee mite Varroa jacobsoni is regulated by host-derived JH. After checking over a thousand capped brood cells containing pupae, it was confirmed that in Apis cerana colonies fertility of female mites is restricted to drone hosts. Apis cerana indica / Apis mellifera ligustica / juvenile hormone titer / reproduction / Varroa ja- cobsoni INTRODUCTION Modern analytical techniques allow the de- termination of hemolymph titer (Rachinsky In honey bees, juvenile hormone (JH) has et al, 1990) and rate of synthesis (Rachin- been studied mostly under aspects of sky and Hartfelder, 1990) even in individu- caste development (Hartfelder, 1990; al bees. Since in arthropods (Downer and Rembold et al, 1992), control of fertility Laufer, 1983) and also in acarids, ticks (Engels et al, 1990), and recently also (Pound and Oliver, 1979; Connat et al, polyethism regulation (Robinson, 1992). -
Population Structure and Classification of Apis Cerana Sarah E
Population structure and classification of Apis cerana Sarah E. Radloff, Colleen Hepburn, H. Randall Hepburn, Stefan Fuchs, Soesilawati Hadisoesilo, Ken Tan, Michael S. Engel, Viktor Kuznetsov To cite this version: Sarah E. Radloff, Colleen Hepburn, H. Randall Hepburn, Stefan Fuchs, Soesilawati Hadisoesilo, et al.. Population structure and classification of Apis cerana. Apidologie, Springer Verlag, 2010, 41(6), 10.1051/apido/2010008. hal-00892035 HAL Id: hal-00892035 https://hal.archives-ouvertes.fr/hal-00892035 Submitted on 1 Jan 2010 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 41 (2010) 589–601 Available online at: c INRA/DIB-AGIB/EDP Sciences, 2010 www.apidologie.org DOI: 10.1051/apido/2010008 Original article Population structure and classification of Apis cerana* Sarah E. Radloff1∗, Colleen Hepburn1,H.RandallHepburn2,StefanFuchs3, Soesilawati Hadisoesilo4,KenTan5, Michael S. Engel6,ViktorKuznetsov** 1 Department of Statistics, Rhodes University, Grahamstown 6140, South Africa 2 Department of Zoology and Entomology, Rhodes University, Grahamstown 6140, South Africa 3 Institut für Bienenkunde, Fachbereich Biowissenschaften, Goethe-Universität Frankfurt am Main, Karl-von- Frisch-Weg 2, 61440 Oberursel, Germany 4 Forest and Nature Conservation Research and Development Centre, Jl.