Wildlife Trade Operation Proposal - Queen Ant Harvesting
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Sperm Use During Egg Fertilization in the Honeybee (Apis Mellifera) Maria Rubinsky SIT Study Abroad
SIT Graduate Institute/SIT Study Abroad SIT Digital Collections Independent Study Project (ISP) Collection SIT Study Abroad Fall 2010 Sperm Use During Egg Fertilization in the Honeybee (Apis Mellifera) Maria Rubinsky SIT Study Abroad Follow this and additional works at: https://digitalcollections.sit.edu/isp_collection Part of the Biology Commons, and the Entomology Commons Recommended Citation Rubinsky, Maria, "Sperm Use During Egg Fertilization in the Honeybee (Apis Mellifera)" (2010). Independent Study Project (ISP) Collection. 914. https://digitalcollections.sit.edu/isp_collection/914 This Unpublished Paper is brought to you for free and open access by the SIT Study Abroad at SIT Digital Collections. It has been accepted for inclusion in Independent Study Project (ISP) Collection by an authorized administrator of SIT Digital Collections. For more information, please contact [email protected]. Sperm use during egg fertilization in the honeybee (Apis mellifera) Maria Rubinsky November, 2010 Supervisors: Susanne Den Boer, Boris Baer, CIBER; The University of Western Australia Perth, Western Australia Academic Director: Tony Cummings Home Institution: Brown University Major: Human Biology- Evolution, Ecosystems, and Environment Submitted in partial fulfillment of the requirements for Australia: Rainforest, Reef, and Cultural Ecology, SIT Study Abroad, Fall 2010 Abstract A technique to quantify sperm use in honeybee queens (Apis mellifera) was developed and used to analyze the number of sperm used in different groups of honeybee queens. To do this a queen was placed on a frame with worker cells containing no eggs, and an excluder box was placed around her. The frame was put back into the colony and removed after two and a half hours. -
Wildlife Trade Operation Proposal – Queen of Ants
Wildlife Trade Operation Proposal – Queen of Ants 1. Title and Introduction 1.1/1.2 Scientific and Common Names Please refer to Attachment A, outlining the ant species subject to harvest and the expected annual harvest quota, which will not be exceeded. 1.3 Location of harvest Harvest will be conducted on privately owned land, non-protected public spaces such as footpaths, roads and parks in Victoria and from other approved Wildlife Trade Operations. Taxa not found in Victoria will be legally sourced from other approved WTOs or collected by Queen of Ants’ representatives from unprotected areas. This may include public spaces such as roadsides and unprotected council parks, and other property privately owned by the representatives. 1.4 Description of what is being harvested Please refer to Attachment A for an outline of the taxa to be harvested. The harvest is of live adult queen ants which are newly mated. 1.5 Is the species protected under State or Federal legislation Ants are non-listed invertebrates and are as such unprotected under Victorian and other State Legislation. Under Federal legislation the only protection to these species relates to the export of native wildlife, which this application seeks to satisfy. No species listed under the EPBC Act as threatened (excluding the conservation dependent category) or listed as endangered, vulnerable or least concern under Victorian legislation will be harvested. 2. Statement of general goal/aims The applicant has recently begun trading queen ants throughout Victoria as a personal hobby and has received strong overseas interest for the species of ants found. -
Analysis of Honeybee Drone Activity During the Mating Season in Northwestern Argentina
insects Article Analysis of Honeybee Drone Activity during the Mating Season in Northwestern Argentina Maria Marta Ayup 1,2,3 , Philipp Gärtner 3, José L. Agosto-Rivera 4, Peter Marendy 5,6 , Paulo de Souza 5,7 and Alberto Galindo-Cardona 1,8,* 1 National Scientific and Technical Research Council, CONICET, CCT, Tucumán 4000, Argentina; [email protected] 2 Faculty of Natural Sciences, National University of Tucumán (UNT), Tucumán 4000, Argentina 3 IER (Regional Ecology Institute), CONICET, Tucumán 4000, Argentina; [email protected] 4 Rio Piedras Campus, University of Puerto Rico, Rio Piedras 00927, Puerto Rico; [email protected] 5 Commonwealth Scientific and Industrial Research Organisation, CSIRO, Canberra 2601, Australia; [email protected] (P.M.); paulo.desouza@griffith.edu.au (P.d.S.) 6 School of Technology, Environments and Design, University of Tasmania, Tasmania 7000, Australia 7 School of Information and Communication Technology, Griffith University, Nathan 4111, Australia 8 Miguel Lillo Foundation, Tucumán 4000, Argentina * Correspondence: [email protected]; Tel.: +54-0381-640-8826 Simple Summary: When we think of social insects, we mostly neglect males and their biology. Honeybee males or drones are an example. Like queens, drones are founders of the colony, but unlike queens and workers, their activity is not well-known. Drones exit the hive to mate as their only goal, in spite of the high chances of getting lost, being preyed upon and starving; and only if they are lucky, they will die when mating. These nuptial flights take place in Drone Congregation Areas during Citation: Ayup, M.M.; Gärtner, P.; spring and summer, and we know that their exit time is in the afternoons. -
Walking with Ants Report by Arminel Ryan
Walking with Ants Report by Arminel Ryan With a mere 45 other participants, I joined lively young ANU myrmecologist, Dr. Ajay Narendra, for a glimpse into the fascinating world of ants - one of the most dominant animals on the planet. Waltraud Pix had organised the adventure, and had had an overwhelming response – more than 200 enquiries! So, at Mt Majura on Sunday 28 February, we fortunate few assembled at 4.30 p.m. for our educational ramble. Our troupe travelled only a short distance in the 2 hours, but the range of fascinating facts that had emerged by 6.30 p.m. was truly phenomenal. I expect you know that ants play a leading role in the environment as predators and scavengers. You may be aware that their social organisation, communication systems and amazing navigation skills have been the object of research for generations. Ajay led us deeper into this world, using a few of the 45 species found on Mount Majura to illustrate his subject. The following is a brief summary of what I gleaned. Australia has around 1,200 species of ant. Ants have evolved from a wasp-like ancestor. Ants differ from wasps (and bees) in three visible anatomical features – . their flexible, conical “waist”, which allows their rear section (called a “gaster”) to flex, . “elbows” in their feelers, and . a metapleural gland that produces antbiotics that helps to prevent the growth of bacteria, fungus, spores on the ant and in its nest. In common with some kinds of wasps and bees, certain ant stings can hurt animals much larger than themselves, but most are harmless to humans. -
Borowiec Et Al-2020 Ants – Phylogeny and Classification
A Ants: Phylogeny and 1758 when the Swedish botanist Carl von Linné Classification published the tenth edition of his catalog of all plant and animal species known at the time. Marek L. Borowiec1, Corrie S. Moreau2 and Among the approximately 4,200 animals that he Christian Rabeling3 included were 17 species of ants. The succeeding 1University of Idaho, Moscow, ID, USA two and a half centuries have seen tremendous 2Departments of Entomology and Ecology & progress in the theory and practice of biological Evolutionary Biology, Cornell University, Ithaca, classification. Here we provide a summary of the NY, USA current state of phylogenetic and systematic 3Social Insect Research Group, Arizona State research on the ants. University, Tempe, AZ, USA Ants Within the Hymenoptera Tree of Ants are the most ubiquitous and ecologically Life dominant insects on the face of our Earth. This is believed to be due in large part to the cooperation Ants belong to the order Hymenoptera, which also allowed by their sociality. At the time of writing, includes wasps and bees. ▶ Eusociality, or true about 13,500 ant species are described and sociality, evolved multiple times within the named, classified into 334 genera that make up order, with ants as by far the most widespread, 17 subfamilies (Fig. 1). This diversity makes the abundant, and species-rich lineage of eusocial ants the world’s by far the most speciose group of animals. Within the Hymenoptera, ants are part eusocial insects, but ants are not only diverse in of the ▶ Aculeata, the clade in which the ovipos- terms of numbers of species. -
Hymenoptera: Formicidae) Along an Elevational Gradient at Eungella in the Clarke Range, Central Queensland Coast, Australia
RAINFOREST ANTS (HYMENOPTERA: FORMICIDAE) ALONG AN ELEVATIONAL GRADIENT AT EUNGELLA IN THE CLARKE RANGE, CENTRAL QUEENSLAND COAST, AUSTRALIA BURWELL, C. J.1,2 & NAKAMURA, A.1,3 Here we provide a faunistic overview of the rainforest ant fauna of the Eungella region, located in the southern part of the Clarke Range in the Central Queensland Coast, Australia, based on systematic surveys spanning an elevational gradient from 200 to 1200 m asl. Ants were collected from a total of 34 sites located within bands of elevation of approximately 200, 400, 600, 800, 1000 and 1200 m asl. Surveys were conducted in March 2013 (20 sites), November 2013 and March–April 2014 (24 sites each), and ants were sampled using five methods: pitfall traps, leaf litter extracts, Malaise traps, spray- ing tree trunks with pyrethroid insecticide, and timed bouts of hand collecting during the day. In total we recorded 142 ant species (described species and morphospecies) from our systematic sampling and observed an additional species, the green tree ant Oecophylla smaragdina, at the lowest eleva- tions but not on our survey sites. With the caveat of less sampling intensity at the lowest and highest elevations, species richness peaked at 600 m asl (89 species), declined monotonically with increasing and decreasing elevation, and was lowest at 1200 m asl (33 spp.). Ant species composition progres- sively changed with increasing elevation, but there appeared to be two gradients of change, one from 200–600 m asl and another from 800 to 1200 m asl. Differences between the lowland and upland faunas may be driven in part by a greater representation of tropical and arboreal-nesting sp ecies in the lowlands and a greater representation of subtropical species in the highlands. -
Diversity of Bacteria in Ants (Hymenoptera: Formicidae) from Canopy and Understory of Selected Trees at Mount Makiling Forest Reserve, Laguna, Philippines
Philippine Journal of Science 150 (3): 753-763, June 2021 ISSN 0031 - 7683 Date Received: 30 Sep 2020 Diversity of Bacteria in Ants (Hymenoptera: Formicidae) from Canopy and Understory of Selected Trees at Mount Makiling Forest Reserve, Laguna, Philippines Michael P. Gatpatan1, Mia Beatriz C. Amoranto1, Alfredo Jose C. Ballesteros3, Noel G. Sabino1, Jocelyn T. Zarate2, Ma. Anita M. Bautista3, and Lucille C. Villegas1* 1Microbiology Division, Institute of Biological Sciences 2National Institute of Molecular Biology and Biotechnology (BIOTECH) University of the Philippines Los Baños, College, Laguna 4031 Philippines 3National Institute of Molecular Biology and Biotechnology (NIMBB) University of the Philippines Diliman, Quezon City 1101 Philippines The Mount Makiling Forest Reserve (MMFR) is a biodiversity hotspot and listed as one of the 170 conservation priority areas established by the Philippine government. Its flora and fauna diversity has been reported, but knowledge gap has been identified concerning the bacterial communities associated with the flora and fauna. This study focused on ants (Hymenoptera: Formicidae), which are dominant in forest canopy and play essential roles in the ecosystem functionality. A metagenomic sequencing approach based on amplified V3–V4 regions of the 16S rRNA was employed to investigate the bacterial communities associated with five arboreal ant species collected from MMFR. The collected ants were identified as Dolichoderus thoracicus, Myrmicaria sp., Colobopsis leonardi, Polyrhachis mindanaensis, and Polyrhachis semiinermis. The sequence analyses revealed that Proteobacteria, Spirochaetes, Firmicutes, Bacteroides, and Actinobacteria were the most abundant phyla. Individual analysis of the bacterial genera associated with the five ant species showed that unclassified members of Rhizobiaceae, Orbaceae, and Burkholderiaceae were dominant in D. -
Iridomyrmex Purpureus)
This is a repository copy of Social and private information influence the decision making of Australian meat ants (Iridomyrmex purpureus). White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/135144/ Version: Accepted Version Article: Middleton, EJT, Reid, CR, Mann, RP orcid.org/0000-0003-0701-1274 et al. (1 more author) (2018) Social and private information influence the decision making of Australian meat ants (Iridomyrmex purpureus). Insectes Sociaux, 65 (4). pp. 649-656. ISSN 0020-1812 https://doi.org/10.1007/s00040-018-0656-1 © International Union for the Study of Social Insects (IUSSI) 2018. This is an author produced version of a paper published in Insectes Sociaux. Uploaded in accordance with the publisher's self-archiving policy. Reuse Items deposited in White Rose Research Online are protected by copyright, with all rights reserved unless indicated otherwise. They may be downloaded and/or printed for private study, or other acts as permitted by national copyright laws. The publisher or other rights holders may allow further reproduction and re-use of the full text version. This is indicated by the licence information on the White Rose Research Online record for the item. 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/ 1 Title: Social and private information influence the decision making of Australian meat ants (Iridomyrmex 2 purpureus) 3 4 Authors: Eliza J.T. -
Did Developing Brood Drive the Evolution of an Obligate Symbiosis
1 Did developing brood drive the evolution 2 of an obligate symbiosis between ants and 3 bacteria? 4 Serafino Teseo1† 5 6 7 1School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive Singapore 8 637551 9 †To whom correspondence should be addressed: [email protected] 10 Keywords: Ants, Primary Endosymbiosis, Camponotini, Camponotus, Blochmannia, Gut Microbes, 11 Bacteriocytes 12 1 13 14 Abstract 15 Blochmannia is a vertically transmitted obligate bacterial symbiont of ants within the tribe 16 Camponotini (Formicidae: Formicinae), hosted in specialized cells (bacteriocytes) of the ant midgut 17 epithelium. Genomic comparisons of Blochmannia with other insect symbionts suggest that the 18 symbiosis may have started with ants tending sap-feeding insects. However, the possible transitions of 19 Blochmannia from mutualist of sap-feeding insects to vertically transmitted organelle-like symbiont of 20 ants have not been formally discussed. Here I propose hypotheses supporting the idea that the ant 21 brood may have had a prominent role in this process. This is mainly because: 1) microbes are more 22 likely to reach the midgut in larvae rather than in adults; 2) bacteriocytes possibly allowed the midgut 23 lumen-dwelling ancestor of Blochmannia to survive gut purging at the onset of the ant pupation, 24 extending its nutritional benefits to metamorphosis; 3) adult ants do not need the nutritional benefits 25 of Blochmannia. Investigating the biology of Camponotini sister taxa may provide further cues regarding 26 the evolution of the symbiosis. 27 2 28 1. Introduction 29 Obligatory symbioses involving intracellular maternally transmitted microorganisms with simplified 30 genomes (primary endosymbioses) are common across insects [1]. -
The Coexistence
Myrmecological News 13 37-55 2009, Online Earlier Natural history and phylogeny of the fungus-farming ants (Hymenoptera: Formicidae: Myrmicinae: Attini) Natasha J. MEHDIABADI & Ted R. SCHULTZ Abstract Ants of the tribe Attini comprise a monophyletic group of approximately 230 described and many more undescribed species that obligately depend on the cultivation of fungus for food. In return, the ants nourish, protect, and disperse their fungal cultivars. Although all members of this tribe cultivate fungi, attine ants are surprisingly heterogeneous with regard to symbiont associations and agricultural system, colony size and social structure, nesting behavior, and mating system. This variation is a key reason that the Attini have become a model system for understanding the evolution of complex symbioses. Here, we review the natural-history traits of fungus-growing ants in the context of a recently published phylo- geny, collating patterns of evolution and symbiotic coadaptation in a variety of colony and fungus-gardening traits in a number of major lineages. We discuss the implications of these patterns and suggest future research directions. Key words: Hymenoptera, Formicidae, fungus-growing ants, leafcutter ants, colony life, natural history, evolution, mating, agriculture, review. Myrmecol. News 13: 37-55 (online xxx 2008) ISSN 1994-4136 (print), ISSN 1997-3500 (online) Received 12 June 2009; revision received 24 September 2009; accepted 28 September 2009 Dr. Natasha J. Mehdiabadi* (contact author) & Dr. Ted R. Schultz* (contact author), Department of Entomology and Laboratories of Analytical Biology, National Museum of Natural History, Smithsonian Institution, P.O. Box 37012, NHB, CE518, MRC 188, Washington, DC 20013-7012, USA. E-mail: [email protected]; [email protected] * Both authors contributed equally to the work. -
Iridomyrmex Purpureus, and Its Taxonomic Significance
4 ¿l 'lcl GENETIC STUDIES OF MEAT A}ITS (tazaouvaunx PunPuaws) . by R, B. Hallida/, B.Sc.(Hons.) Department of Genetics University of Adelaide. A thesis subnitted to the University of Adelaide for the degree of Doctor of Philosophy, in May, 1978' TABLE QF 'CONTENTS Page SUMMARY i DECLARATION ].V ACKNOWLEDGEMENTS v CHAPTER 1 INTRODUCTION I CHAPTER 2 ECOLOGY AND SYSTET{ATICS OF MEAT A¡ITS 4 2,L Taxonomic background 4 2.2 Appearance of colour forms 7 2.3 Geographic distribution 10 2.4 Interactions between colour fonts T2 2.5 Mating and colony founding 15 2.6 Nest structure T7 2.7 Colony and popu3..ation structure 20 2.8 General biology and pest status 24 ?o 0verview 28 CHAPTER J MATERIALS AND METHODS 29 3 I Populations sanpled 29 3 2 Collection nethods 38 3.3 Sanple preparation 59 3.4 Electrophoresis nethods 40 3.5 Gel staining nethods 42 3.6 Chronosome nethods 47 CHAPTER 4 POLYMORPHISM AT TÍ{Ë AMYT,ASE LOCUS 48 4.L The phenotypes and their inheritance 48 4.2 Estination of gene frequencies 51 4.3 Geographic variation within forms 56 4.4 Differences anong forrns 58 POLYMORPHISM AT THE ESTERÄSE=] LOCUS 61 The phenotypes and their inheritance 6L Estination of gene frequencies 63 Within and between fo::rn variation 65 Discussion 67 CHAPTER 6 OTHER ISOZYME LQCI IN MEAT ANTS 69 6.1 Aldehgde. oxÍdase 69 6.2 Esüerase-2 70 6.3 Esterase:3 72 6.4 General protein 74 6.s G Tuco se*6 -.p/:o sphate dehgdrog enase 75 6.6 G Tutamate dehgclrogenase 76 6.7 Lactate dehgdrogenase 77 6.8 Leucíne amÍnopeptÌdase 78 6.9 I{alate dehgdrogenase 79 6. -
Formicidae: Catalogue of Family-Group Taxa
FORMICIDAE: CATALOGUE OF FAMILY-GROUP TAXA [Note (i): the standard suffixes of names in the family-group, -oidea for superfamily, –idae for family, -inae for subfamily, –ini for tribe, and –ina for subtribe, did not become standard until about 1905, or even much later in some instances. Forms of names used by authors before standardisation was adopted are given in square brackets […] following the appropriate reference.] [Note (ii): Brown, 1952g:10 (footnote), Brown, 1957i: 193, and Brown, 1976a: 71 (footnote), suggested the suffix –iti for names of subtribal rank. These were used only very rarely (e.g. in Brandão, 1991), and never gained general acceptance. The International Code of Zoological Nomenclature (ed. 4, 1999), now specifies the suffix –ina for subtribal names.] [Note (iii): initial entries for each of the family-group names are rendered with the most familiar standard suffix, not necessarily the original spelling; hence Acanthostichini, Cerapachyini, Cryptocerini, Leptogenyini, Odontomachini, etc., rather than Acanthostichii, Cerapachysii, Cryptoceridae, Leptogenysii, Odontomachidae, etc. The original spelling appears in bold on the next line, where the original description is cited.] ACANTHOMYOPSINI [junior synonym of Lasiini] Acanthomyopsini Donisthorpe, 1943f: 618. Type-genus: Acanthomyops Mayr, 1862: 699. Taxonomic history Acanthomyopsini as tribe of Formicinae: Donisthorpe, 1943f: 618; Donisthorpe, 1947c: 593; Donisthorpe, 1947d: 192; Donisthorpe, 1948d: 604; Donisthorpe, 1949c: 756; Donisthorpe, 1950e: 1063. Acanthomyopsini as junior synonym of Lasiini: Bolton, 1994: 50; Bolton, 1995b: 8; Bolton, 2003: 21, 94; Ward, Blaimer & Fisher, 2016: 347. ACANTHOSTICHINI [junior synonym of Dorylinae] Acanthostichii Emery, 1901a: 34. Type-genus: Acanthostichus Mayr, 1887: 549. Taxonomic history Acanthostichini as tribe of Dorylinae: Emery, 1901a: 34 [Dorylinae, group Cerapachinae, tribe Acanthostichii]; Emery, 1904a: 116 [Acanthostichii]; Smith, D.R.