Yellow Crazy Ants Anoplolepis Gracilipes
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Field Guide of Common Ants
J U L Y / A U G 2 0 0 3 N P M A L I B R A R Y U P D A T E Insert this update into the NPMA Pest Management Library, which can be Updatepurchased from the Resource Center. phone: 703-573-8330 fax: 703-573-4116 Common Ants: A Pull-Out Guide for Use in the Field This Library Update is designed to of acrobat ants. Workers are 1/16” to 1/8” assist technicians in identification and in length and are normally brown to control of ants while servicing accounts. black in color. The pedicel, or front joint This update is not designed for of the abdomen has two nodes or instruction in basic ant biology, segments. Looking down on the ant nomenclature of the anatomy of the ant, under hand lens magnification, one pair or to be used as a key. For more detailed of spines is found on the thorax. Various information on those topics, refer to the species of acrobat ants are found Field Guide or other technical materials. throughout the United States. In the field, a great aid to identification Acrobat ants are named for their is the use of a hand lens. Many of these tendency to raise their abdomens in the ants are small and positive identification air when disturbed. As the abdomen is is not easy without a hand lens. This heart shaped and is frequently black and article focuses on common, non-wood- shiny, the acrobat motion is readily destroying ants, including: acrobat, observable. -
Taxonomy and Distribution of the Argentine Ant, Linepithema Humile (Hymenoptera: Formicidae)
SYSTEMATICS Taxonomy and Distribution of the Argentine Ant, Linepithema humile (Hymenoptera: Formicidae) ALEXANDER L. WILD Department of Entomology, University of California at Davis, Davis, CA 95616 Ann. Entomol. Soc. Am. 97(6): 1204Ð1215 (2004) ABSTRACT The taxonomy of an invasive pest species, the Argentine ant, is reviewed. Linepithema humile (Mayr) 1868 is conÞrmed as the valid name for the Argentine ant. Morphological variation and species boundaries of L. humile are examined, with emphasis on populations from the antÕs native range in southern South America. Diagnoses and illustrations are provided for male, queen, and worker castes. Collection records of L. humile in South America support the idea of a native distribution closely associated with major waterways in lowland areas of the Parana´ River drainage, with recent intro- ductions into parts of Argentina, Brazil, Chile, Colombia, Ecuador, and Peru. KEY WORDS Argentine ant, Linepithema humile, taxonomy, invasive species THE ARGENTINE ANT, Linepithema humile (Mayr) 1868, MCSN, MCZC, MHNG, MZSP, NHMB, NHMW, and is among the worldÕs most successful invasive species. USNM; see below for explanation of abbreviations). This native South American insect has become a cos- Taxonomic confusion over L. humile extends be- mopolitan pest, particularly in the Mediterranean cli- yond museum collections. At least one important mates of North America, Chile, South Africa, Austra- study, seeking to explain Argentine ant population lia, and southern Europe (Suarez et al. 2001). regulation in the native range through phorid para- Argentine ants have been implicated in the decline of sitism (Orr and Seike 1998), initially targeted the native arthropod (Cole et al. 1992) and vertebrate wrong Linepithema species (Orr et al. -
James K. Wetterer
James K. Wetterer Wilkes Honors College, Florida Atlantic University 5353 Parkside Drive, Jupiter, FL 33458 Phone: (561) 799-8648; FAX: (561) 799-8602; e-mail: [email protected] EDUCATION UNIVERSITY OF WASHINGTON, Seattle, WA, 9/83 - 8/88 Ph.D., Zoology: Ecology and Evolution; Advisor: Gordon H. Orians. MICHIGAN STATE UNIVERSITY, East Lansing, MI, 9/81 - 9/83 M.S., Zoology: Ecology; Advisors: Earl E. Werner and Donald J. Hall. CORNELL UNIVERSITY, Ithaca, NY, 9/76 - 5/79 A.B., Biology: Ecology and Systematics. UNIVERSITÉ DE PARIS III, France, 1/78 - 5/78 Semester abroad: courses in theater, literature, and history of art. WORK EXPERIENCE FLORIDA ATLANTIC UNIVERSITY, Wilkes Honors College 8/04 - present: Professor 7/98 - 7/04: Associate Professor Teaching: Biodiversity, Principles of Ecology, Behavioral Ecology, Human Ecology, Environmental Studies, Tropical Ecology, Field Biology, Life Science, and Scientific Writing 9/03 - 1/04 & 5/04 - 8/04: Fulbright Scholar; Ants of Trinidad and Tobago COLUMBIA UNIVERSITY, Department of Earth and Environmental Science 7/96 - 6/98: Assistant Professor Teaching: Community Ecology, Behavioral Ecology, and Tropical Ecology WHEATON COLLEGE, Department of Biology 8/94 - 6/96: Visiting Assistant Professor Teaching: General Ecology and Introductory Biology HARVARD UNIVERSITY, Museum of Comparative Zoology 8/91- 6/94: Post-doctoral Fellow; Behavior, ecology, and evolution of fungus-growing ants Advisors: Edward O. Wilson, Naomi Pierce, and Richard Lewontin 9/95 - 1/96: Teaching: Ethology PRINCETON UNIVERSITY, Department of Ecology and Evolutionary Biology 7/89 - 7/91: Research Associate; Ecology and evolution of leaf-cutting ants Advisor: Stephen Hubbell 1/91 - 5/91: Teaching: Tropical Ecology, Introduction to the Scientific Method VANDERBILT UNIVERSITY, Department of Psychology 9/88 - 7/89: Post-doctoral Fellow; Visual psychophysics of fish and horseshoe crabs Advisor: Maureen K. -
The Case of the Argentine Ant in Vineyards of Northern Argentina
insects Article Growing Industries, Growing Invasions? The Case of the Argentine Ant in Vineyards of Northern Argentina Maria Schulze-Sylvester 1,* ID , José A. Corronca 1 ID and Carolina I. Paris 2 1 FCN-IEBI (Instituto para el Estudio de la Biodiversidad de Invertebrados), CONICET CCT-Salta, Facultad de Ciencias Naturales, Universidad Nacional de Salta, Av. Bolivia 5150, CP 4400 Salta, Argentina; [email protected] 2 Departamento de Ecología, Genética y Evolución, Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Buenos Aires, 1428 Buenos Aires, Argentina; [email protected] * Correspondence: [email protected]; Tel.: +54-387-425-5472 Received: 10 December 2017; Accepted: 23 January 2018; Published: 29 January 2018 Abstract: The invasive Argentine ant causes ecological and economic damage worldwide. In 2011, this species was reported in vineyards of Cafayate, a wine-producing town in the Andes, Argentina. While the local xeric climate is unsuitable for Argentine ants, populations could establish in association with vineyards where human activity and irrigation facilitate propagule introduction and survival. In 2013–2014, we combined extensive sampling of the area using ant-baits with monitoring of the change in land use and vineyard cultivated area over the past 15 years. Our results revealed that the species has thus far remained confined to a relatively isolated small area, owing to an effective barrier of dry shrublands surrounding the infested vineyards; yet the recent expansion of vineyard acreage in this region will soon connect this encapsulated area with the rest of the valley. When this happens, vulnerable ecosystems and the main local industry will be put at risk. -
US EPA-Pesticides; Disodium Octaborate Tetrahydrate
EFFICACY REVIEW DATE: IN 4-30-01 OUT 6-21-01 FILE OR REG. NO. 69529-1 PETITION OR EXP. PERMIT NO. DATE DIV. RECEIVED April 19, 2001 DATE OF SUBMISSION April 18, 2001 DATE SUBMISSION ACCEPTED TYPE PRODUCT(S): (I,)D, H, F, N, R, S DATA ACCESSION NO(S). 453568-01;D274488;S596027;Case#046539;AC:301 PRODUCT MGR. NO. 03-Layne/Quarles PRODUCT NAME(S) Pestbor COMPANY NAME Quality Borate Company SUBMISSION PURPOSE Provide performance data in reprint supporting claims for Argentine ant, pharaoh ant and Tap- inoma melanocephalum for formulated products. CHEMICAL & FORMULATION Disodium octaborate tetrahydrate 98% (30 lbs./cu.ft. bulk density manufacturing concentrate) CONCLUSIONS & RECOMMENDATIONS The data presented in EPA Accession (MRID) Number 453568-01, having been obtained from the reprint art- icle titled “Laboratory Evaluation of a Boric Acid Liquid Bait on Colonies of Tapinoma melanocephalum, Argentine Ants and Pharaoh Ants (Hymenoptera: Formicidae)S, which meets the requirements of § 11(b)(1)-(7) on p. 268 and the standard of § 95-11(c)(3)(b) on pp. 270-1 of the Product Performance Guidelines, are adequate to sup- port the registration of the subject product, the sole use for this formulation being for the manufacturing of end use insecticidal products, more specifically baits. The cited data (to be contin'd) is far more than is necessary to establish usefulness of this form- ulation for the making of insecticidal baits. Results with the 3 species included in the testing were as follows: Tapinoma melanocephalum workers were reduced by 97% -
Above-Belowground Effects of the Invasive Ant Lasius Neglectus in an Urban Holm Oak Forest
U B Universidad Autónoma de Barce lona Departamento de Biología Animal, de Biología Vegetal y de Ecología Unidad de Ecología Above-belowground effects of the invasive ant Lasius neglectus in an urban holm oak forest Tesis doctoral Carolina Ivon Paris Bellaterra, Junio 2007 U B Universidad Autónoma de Barcelona Departamento de Biología Animal, de Biología Vegetal y de Ecología Unidad de Ecología Above-belowground effects of the invasive ant Lasius neglectus in an urban holm oak forest Memoria presentada por: Carolina Ivon Paris Para optar al grado de Doctora en Ciencias Biológicas Con el Vº. Bº.: Dr Xavier Espadaler Carolina Ivon Paris Investigador de la Unidad de Ecología Doctoranda Director de tesis Bellaterra, Junio de 2007 A mis padres, Andrés y María Marta, y a mi gran amor Pablo. Agradecimientos. En este breve texto quiero homenajear a través de mi más sincero agradecimiento a quienes me ayudaron a mejorar como persona y como científica. Al Dr Xavier Espadaler por admitirme como doctoranda, por estar siempre dispuesto a darme consejos tanto a nivel profesional como personal, por darme la libertad necesaria para crecer como investigadora y orientarme en los momentos de inseguridad. Xavier: nuestras charlas más de una vez trascendieron el ámbito académico y fue un gustazo escucharte y compartir con vos algunos almuerzos. Te prometo que te enviaré hormigas de la Patagonia Argentina para tu deleite taxonómico. A Pablo. ¿Qué puedo decirte mi amor qué ya no te haya dicho? Gracias por la paciencia, el empuje y la ayuda que me diste en todo momento. Estuviste atento a los más mínimos detalles para facilitarme el trabajo de campo y de escritura. -
The Action Plan for Australian Birds 2000: Recovery Outline
RECOVERY OUTLINE Christmas Island Imperial-Pigeon 1 Family Columbidae 2 Scientific name Ducula whartoni (Sharpe, 1887) 3 Common name Christmas Island Imperial-Pigeon 4 Conservation status Critically Endangered: A2ce 5 Reasons for listing 9 Ecology The population size of this subspecies is expected to The Christmas Island Imperial-Pigeon is found mainly decrease by up to 80% over the next three generations on the inland plateau in rainforest and, to some extent, (12 years; Critically Endangered: A2) as a result of a in secondary regrowth dominated by the introduced decline in habitat quality (c) and the current rate of Japanese Cherry Muntingia calabura (Crome, 1987, spread of introduced ants (e). Stokes, 1988). It nests in the top of rainforest trees and other dense vegetation (Hicks and Yorkston, 1982), Estimate Reliability and feeds on rainforest and other fruits, as well as 2 Extent of occurrence 137 km high buds and leaves (Higgins and Davies, 1996). trend stable high 10 Threats Area of occupancy 100 km2 high In the past, numbers of Christmas Island Imperial trend decreasing medium Pigeon have been reduced by habitat clearance and No. of breeding birds 1,000 low hunting (Crome, 1987, Stokes, 1988). About one-third trend decreasing medium of the pigeon's preferred plateau forest was cleared for No. of sub-populations 1 high phosphate mining before this ceased in 1987, though Generation time 5 years low this loss has been partly offset by introduction of the 6 Infraspecific taxa Japanese Cherry, which flourishes on many former None described. mine fields and other disturbed areas, and provides a rich food source for much of the year (Stokes, 1988). -
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. -
Impact of the Invasive Crazy Ant Anoplolepis Gracilipes on Bird Island, Seychelles
Journal of Insect Conservation 8: 15–25, 2004. 15 # 2004 Kluwer Academic Publishers. Printed in the Netherlands. Impact of the invasive crazy ant Anoplolepis gracilipes on Bird Island, Seychelles J. Gerlach University Museum of Zoology Cambridge, Department of Zoology, Downing Street, Cambridge CB2 3EJ, UK (e-mail: [email protected]) Received 26 March 2003; accepted in revised form 12 December 2003 Key words: Anoplolepis gracilipes, Ant, Formicidae, Invasion, Management, Seychelles Abstract The crazy ant (Anoplolepis gracilipes) invaded Bird island, Seychelles, in the 1980s. In 1997, its range expanded and population densities increased. The impacts of this change were studied in 2001 using a combination of arthropod collecting methods. The ant population excluded larger invertebrates (principally the large ant Odontomachus simillimus and the crabs, principally Ocypode spp.). Cockroaches, however, remained abundant in ant-infested areas and tree-nesting birds (Lesser Noddy Anous tenuirostris) appear to be able to breed successfully in the presence of the crazy ant. The ants are only abundant in areas of deep shade which provide cool nesting areas, yet enabling them to forage in the open when ground temperatures fall. The expansion of the ants was correlated with the regeneration of woodland on the island. Recommendations are made for the management of the woodland which may reduce the impacts of the crazy ant. Introduction Africa, Asia, America and Australia (Dorow 1996). This species has been recorded as excluding The threat from alien invasive species is widely other ant species (Greenslade 1971) and recently perceived as one of the major contributions to has been implicated in a population crash in the present-day high-extinction rates, affecting an esti- red crab Gecarcoidea natalis on Christmas Island mated 30% of threatened birds, 15% of threatened (O’ Dowd et al. -
Deformed Wing Virus in Two Widespread Invasive Ants: Geographical Distribution, Prevalence, and Phylogeny
viruses Article Deformed Wing Virus in Two Widespread Invasive Ants: Geographical Distribution, Prevalence, and Phylogeny Chun-Yi Lin 1 , Chih-Chi Lee 1,2 , Yu-Shin Nai 3 , Hung-Wei Hsu 1,2, Chow-Yang Lee 4 , Kazuki Tsuji 5 and Chin-Cheng Scotty Yang 3,6,* 1 Research Institute for Sustainable Humanosphere, Kyoto University, Kyoto 611-0011, Japan; [email protected] (C.-Y.L.); [email protected] (C.-C.L.); [email protected] (H.-W.H.) 2 Laboratory of Insect Ecology, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502, Japan 3 Department of Entomology, National Chung Hsing University, Taichung 402204, Taiwan; [email protected] 4 Department of Entomology, University of California, 900 University Avenue, Riverside, CA 92521, USA; [email protected] 5 Department of Subtropical Agro-Environmental Sciences, University of the Ryukyus, Senbaru 1, Nishihara, Okinawa 903-0213, Japan; [email protected] 6 Department of Entomology, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA * Correspondence: [email protected]; Tel.: +886-4-2284-0361 (ext. 540) Received: 16 October 2020; Accepted: 13 November 2020; Published: 15 November 2020 Abstract: Spillover of honey bee viruses have posed a significant threat to pollination services, triggering substantial effort in determining the host range of the viruses as an attempt to understand the transmission dynamics. Previous studies have reported infection of honey bee viruses in ants, raising the concern of ants serving as a reservoir host. Most of these studies, however, are restricted to a single, local ant population. We assessed the status (geographical distribution/prevalence/viral replication) and phylogenetic relationships of honey bee viruses in ants across the Asia–Pacific region, using deformed wing virus (DWV) and two widespread invasive ants, Paratrechina longicornis and Anoplolepis gracilipes, as the study system. -
Yellow Crazy Ant (364) Relates To: Ants
Pacific Pests, Pathogens & Weeds - Fact Sheets https://apps.lucidcentral.org/ppp/ Yellow crazy ant (364) Relates to: Ants Photo 1. Side view of worker, yellow crazy ant, Photo 2. View from above of worker, yellow crazy ant, Anoplolepis gracilipes. Anoplolepis gracilipes. Photo 3. Front of head of worker, yellow crazy ant, Photo 4. Side view of queens, yellow crazy ant, Anoplolepis gracilipes. Anoplolepis gracilipes. Common Name Yellow crazy ant, long-legged ant Scientific Name Anoplolepis gracilipes Distribution Worldwide. Particularly, lowland tropical forests. Asia, Africa (restricted), North (restricted), South, and Central (restricted) America, Oceania. It is recorded from Australia, Cook Islands, Federated States of Micronesia, Fiji, French Polynesia, Guam, Kiribati, Marshall Islands, New Caledonia, Niue, Northern Mariana Islands, Palau, Papua New Guinea, Samoa, Solomon Islands, Tokelau, Tonga, Tuvalu, Vanuatu, Wallis and Futuna Islands. Hosts An ant that favours disturbed agricultural and forest habitats, mostly below 1200 m. It can invade urban areas and become a serious household pest. Many crops are hosts, the attraction being the honeydew from sap-sucking insects: banana, cinnamon, citrus, cocoa, coconut, coffee, durian, mango, rambutan, sugarcane. Symptoms & Life Cycle The ant is yellow-brown or reddish-brown, with a slender body about 5 mm long, large eyes, extremely long antennae, and a gaster (the large, bulbous part of the abdomen, see photos) darker than the rest of the body (Photo 1-3). All the workers are of similar size. Its fast, seemingly uncontrolled movements, are the reason for its common name. It does not sting, but it can overcome or kill prey by spraying formic acid. -
University of Florida Thesis Or Dissertation Formatting
FORAGING STRATEGIES AND AGGRESSION PATTERNS OF NYLANDERIA FULVA (Mayr) (HYMENOPTERA: FORMICIDAE) IN NORTH CENTRAL FLORIDA By STEPHANIE KAY HILL A DISSERTATION PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY UNIVERSITY OF FLORIDA 2013 1 © 2013 Stephanie Kay Hill 2 To my family and friends that shared in this journey with me 3 ACKNOWLEDGMENTS I express my deepest appreciation to all the folks who helped and guided me through my graduate studies. My many thanks and gratitude to my major professor, Dr. Phil Koehler, for all of his encouragement, dedication, patience, and guidance. I would especially like the thank Dr. Roberto Pereira for his time and patience as we went through statistical processes and editing. I gratefully thank Dr. Grady Roberts for mentoring me through my agricultural education minor. Thanks to Dr. David Williams for all of his support and keeping me on the ball. Dr. Rebecca Baldwin, thank you for being my mentor and allowing me to have so many teaching experiences. A huge thank you and my upmost respect to Mark Mitola. I was lucky to have you assist me. We have many memories that I hope we can reminisce over years down the road. Thank you to the ever wonderful Liz Pereira and Tiny Willis. Without the two of you, the Urban Lab would fall apart. Thank you to my closest and dearest lab mates: Jodi Scott, Bennett Jordan, Joe DiClaro, Anda Chaskopoulou, Margie Lehnert, and Ricky Vazquez In particular, Jodi provided me with support and comic relief.