Ants and Their Relation to Aphids Charles Richardson Jones Iowa State College
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CA-Dec12-Doc.6.2.A
CA-Dec12-Doc.6.2.a - Final PRODUCT TYPE 18 – INSECTICIDES, ACARICIDES AND PRODUCTS TO CONTROL OTHER ARTHROPODS and PRODUCT TYPE 19 – REPELLENTS AND ATTRACTANTS (only concerning arthropods) Guidance to replace part of Appendices to chapter 7 (page 187 to 200) from TNsG on Product Evaluation Reader ................................................................................................................................... 5 1 GENERAL INTRODUCTION .............................................................................................. 5 1.1 Aim ........................................................................................................................... 5 1.2 Global structure of the assessment .......................................................................... 5 1.3 Dossier requirements ............................................................................................... 5 1.3.1 Test design ....................................................................................................... 6 1.3.2 Test examples ................................................................................................... 7 1.3.3 Laboratory versus (semi) field trials ................................................................... 7 1.3.4 The importance of controls on efficacy studies .................................................. 7 1.3.5 Specific data to support label claims ................................................................. 8 1.3.6 Examples of specific label claims with respect to target -
Buczkowski G. and Krushelnycky P. 2011. the Odorous House Ant
Myrmecological News 16 61-66 Online Earlier, for print 2012 The odorous house ant, Tapinoma sessile (Hymenoptera: Formicidae), as a new temperate-origin invader Grzegorz BUCZKOWSKI & Paul KRUSHELNYCKY Abstract A population of the odorous house ant, Tapinoma sessile, was found at an upland site on Maui, Hawaii. Although T. sessile possesses many of the traits shared by most invasive ant species and is a significant urban pest in the continental USA, this represents the first confirmed record for this species outside its native North American range. Our survey of the site revealed a relatively large (ca. 17 ha) infestation with many closely spaced nests, possibly all belonging to a single supercolony as suggested by the lack of aggression or only occasional non-injurious aggression between workers from distant nests. The odorous house ant is currently abundant at this site, despite the presence of seven other intro- duced ant species, including the big-headed ant (Pheidole megacephala) and the Argentine ant (Linepithema humile). Based on its behavior at this site, T. sessile may successfully invade other temperate areas in the future, and should be watched for by biosecurity programs. Key words: Invasive ants, odorous house ant, Tapinoma sessile, Hawaii. Myrmecol. News 16: 61-66 (online xxx 2010) ISSN 1994-4136 (print), ISSN 1997-3500 (online) Received 26 April 2011; revision received 13 July 2011; accepted 28 July 2011 Subject Editor: Philip J. Lester Grzegorz Buczkowski (contact author), Department of Entomology, Purdue University, West Lafayette, IN 47907, USA. E-mail: [email protected] Paul Krushelnycky, Department of Plant and Environmental Protection Sciences, University of Hawaii, Honolulu, HI 96822, USA. -
Somerset's Ecological Network
Somerset’s Ecological Network Mapping the components of the ecological network in Somerset 2015 Report This report was produced by Michele Bowe, Eleanor Higginson, Jake Chant and Michelle Osbourn of Somerset Wildlife Trust, and Larry Burrows of Somerset County Council, with the support of Dr Kevin Watts of Forest Research. The BEETLE least-cost network model used to produce Somerset’s Ecological Network was developed by Forest Research (Watts et al, 2010). GIS data and mapping was produced with the support of Somerset Environmental Records Centre and First Ecology Somerset Wildlife Trust 34 Wellington Road Taunton TA1 5AW 01823 652 400 Email: [email protected] somersetwildlife.org Front Cover: Broadleaved woodland ecological network in East Mendip Contents 1. Introduction .................................................................................................................... 1 2. Policy and Legislative Background to Ecological Networks ............................................ 3 Introduction ............................................................................................................... 3 Government White Paper on the Natural Environment .............................................. 3 National Planning Policy Framework ......................................................................... 3 The Habitats and Birds Directives ............................................................................. 4 The Conservation of Habitats and Species Regulations 2010 .................................. -
Akes an Ant an Ant? Are Insects, and Insects Are Arth Ropods: Invertebrates (Animals With
~ . r. workers will begin to produce eggs if the queen dies. Because ~ eggs are unfertilized, they usually develop into males (see the discus : ~ iaplodiploidy and the evolution of eusociality later in this chapter). =- cases, however, workers can produce new queens either from un ze eggs (parthenogenetically) or after mating with a male ant. -;c. ant colony will continue to grow in size and add workers, but at -: :;oint it becomes mature and will begin sexual reproduction by pro· . ~ -irgin queens and males. Many specie s produce males and repro 0 _ " females just before the nuptial flight . Others produce males and ---: : ._ tive fem ales that stay in the nest for a long time before the nuptial :- ~. Our largest carpenter ant, Camponotus herculeanus, produces males _ . -:= 'n queens in late summer. They are groomed and fed by workers :;' 0 it the fall and winter before they emerge from the colonies for their ;;. ights in the spring. Fin ally, some species, including Monomoriurn : .:5 and Myrmica rubra, have large colonies with multiple que ens that .~ ..ew colonies asexually by fragmenting the original colony. However, _ --' e polygynous (literally, many queens) and polydomous (literally, uses, referring to their many nests) ants eventually go through a -">O=- r' sexual reproduction in which males and new queens are produced. ~ :- . ant colony thus functions as a highly social, organ ized "super _ _ " 1." The queens and mo st workers are safely hidden below ground : : ~ - ed within the interstices of rotting wood. But for the ant workers ~ '_i S ' go out and forage for food for the colony,'life above ground is - =- . -
Rapid Determination of Sperm Number in Ant Queens by Flow Cytometry
Insect. Soc. 55 (2008) 283 – 287 0020-1812/08/030283-5 Insectes Sociaux DOI 10.1007/s00040-008-1003-8 Birkhuser Verlag, Basel, 2008 Research article Rapid determination of sperm number in ant queens by flow cytometry L. Cournault and S. Aron Behavioral and Evolutionary Ecology, Universit Libre de Bruxelles, Belgium, e-mail: [email protected], [email protected] Received 22 February 2008 ; revised 7 April 2008 ; accepted 9 April 2008. Published Online First 6 May 2008 Abstract. In social Hymenoptera, queens receive a given sperm transfer and sperm utilization (see review of Page, amount of sperm during a single or multiple insemina- 1986; ants: Keller and Passera, 1992; Reichardt and tions once and for all. The amount of sperm stored at Wheeler, 1996; Wiernasz et al., 2001), queen longevity mating determines the maximum number of fertilized and age from sperm depletion (ants: Tschinkel, 1987), eggs queens can produce for the rest of their reproductive sperm production and sperm competition (bumble bees: life. We propose flow cytometry (FCM) as a method to Duchateau and Marin, 1995; honeybees: Moritz, 1986; estimate the concentration of sperm cells, as well as their Woyciechowski and Krol, 1996), or for tests of hypotheses ploidy level, in queens spermathecae. Our data, obtained on the evolution of multiple mating (e.g., “multiple- from 5 ant species, show that FCM is precise, repeatable, mating-for-more-sperm hypothesis”; ants: Fjerdingstad easy to conduct and rapid. Estimates of variation of and Boomsma, 1998; Pearcy et al., submitted). spermathecal content always remain below 10%, and To date, estimation of the number of spermatozoa samples can be analysed in less than 5 minutes. -
UC Riverside UC Riverside Electronic Theses and Dissertations
UC Riverside UC Riverside Electronic Theses and Dissertations Title Food Preference, Survivorship, and Intraspecific Interactions of Velvety Tree Ants Permalink https://escholarship.org/uc/item/75r0k078 Author Hoey-Chamberlain, Rochelle Publication Date 2012 Peer reviewed|Thesis/dissertation eScholarship.org Powered by the California Digital Library University of California UNIVERSITY OF CALIFORNIA RIVERSIDE Food Preference, Survivorship, and Intraspecific Interactions of Velvety Tree Ants A Thesis submitted in partial satisfaction of the requirements for the degree of Master of Science in Entomology by Rochelle Viola Hoey-Chamberlain December 2012 Thesis Committee: Dr. Michael K. Rust, Chairperson Dr. Ring Cardé Dr. Gregory P. Walker Copyright by Rochelle Viola Hoey-Chamberlain 2012 The Thesis of Rochelle Viola Hoey-Chamberlain is approved: Committee Chairperson University of California, Riverside ACKNOWLEDGMENTS In part this research was supported by the Carl Strom Western Exterminator Scholarship. Thank you to Jeremy Brown for his assistance in all projects including collecting ant colonies, setting up food preference trials, setting up and collecting data during nestmate recognition studies and supporting other aspects of the field work. Thank you also to Dr. Les Greenburg (UC Riverside) for guidance and support with many aspects of these projects including statistics and project ideas. Thank you to Dr. Greg Walker (UC Riverside) and Dr. Laurel Hansen (Spokane Community College) for their careful review of the manuscript. Thank you to Dr. Subir Ghosh for assistance with statistics for the survival study. And thank you to Dr. Paul Rugman-Jones for his assistance with the genetic analyses. iv ABSTRACT OF THE THESIS Food Preference, Survivorship, and Intraspecific Interactions of Velvety Tree Ants by Rochelle Viola Hoey-Chamberlain Master of Science, Graduate Program in Entomology University of California, Riverside, December 2012 Dr. -
Through Arthropod Eyes Gaining Mechanistic Understanding of Calcareous Grassland Diversity
Through arthropod eyes Gaining mechanistic understanding of calcareous grassland diversity Toos van Noordwijk Through arthropod eyes Gaining mechanistic understanding of calcareous grassland diversity Van Noordwijk, C.G.E. 2014. Through arthropod eyes. Gaining mechanistic understanding of calcareous grassland diversity. Ph.D. thesis, Radboud University Nijmegen, the Netherlands. Keywords: Biodiversity, chalk grassland, dispersal tactics, conservation management, ecosystem restoration, fragmentation, grazing, insect conservation, life‑history strategies, traits. ©2014, C.G.E. van Noordwijk ISBN: 978‑90‑77522‑06‑6 Printed by: Gildeprint ‑ Enschede Lay‑out: A.M. Antheunisse Cover photos: Aart Noordam (Bijenwolf, Philanthus triangulum) Toos van Noordwijk (Laamhei) The research presented in this thesis was financially spupported by and carried out at: 1) Bargerveen Foundation, Nijmegen, the Netherlands; 2) Department of Animal Ecology and Ecophysiology, Institute for Water and Wetland Research, Radboud University Nijmegen, the Netherlands; 3) Terrestrial Ecology Unit, Ghent University, Belgium. The research was in part commissioned by the Dutch Ministry of Economic Affairs, Agriculture and Innovation as part of the O+BN program (Development and Management of Nature Quality). Financial support from Radboud University for printing this thesis is gratefully acknowledged. Through arthropod eyes Gaining mechanistic understanding of calcareous grassland diversity Proefschrift ter verkrijging van de graad van doctor aan de Radboud Universiteit Nijmegen op gezag van de rector magnificus prof. mr. S.C.J.J. Kortmann volgens besluit van het college van decanen en ter verkrijging van de graad van doctor in de biologie aan de Universiteit Gent op gezag van de rector prof. dr. Anne De Paepe, in het openbaar te verdedigen op dinsdag 26 augustus 2014 om 10.30 uur precies door Catharina Gesina Elisabeth van Noordwijk geboren op 9 februari 1981 te Smithtown, USA Promotoren: Prof. -
The Evolution of Social Parasitism in Formica Ants Revealed by a Global Phylogeny – Supplementary Figures, Tables, and References
The evolution of social parasitism in Formica ants revealed by a global phylogeny – Supplementary figures, tables, and references Marek L. Borowiec Stefan P. Cover Christian Rabeling 1 Supplementary Methods Data availability Trimmed reads generated for this study are available at the NCBI Sequence Read Archive (to be submit ted upon publication). Detailed voucher collection information, assembled sequences, analyzed matrices, configuration files and output of all analyses, and code used are available on Zenodo (DOI: 10.5281/zen odo.4341310). Taxon sampling For this study we gathered samples collected in the past ~60 years which were available as either ethanol preserved or pointmounted specimens. Taxon sampling comprises 101 newly sequenced ingroup morphos pecies from all seven species groups of Formica ants Creighton (1950) that were recognized prior to our study and 8 outgroup species. Our sampling was guided by previous taxonomic and phylogenetic work Creighton (1950); Francoeur (1973); Snelling and Buren (1985); Seifert (2000, 2002, 2004); Goropashnaya et al. (2004, 2012); Trager et al. (2007); Trager (2013); Seifert and Schultz (2009a,b); MuñozLópez et al. (2012); Antonov and Bukin (2016); Chen and Zhou (2017); Romiguier et al. (2018) and included represen tatives from both the New and the Old World. Collection data associated with sequenced samples can be found in Table S1. Molecular data collection and sequencing We performed nondestructive extraction and preserved samespecimen vouchers for each newly sequenced sample. We remounted all vouchers, assigned unique specimen identifiers (Table S1), and deposited them in the ASU Social Insect Biodiversity Repository (contact: Christian Rabeling, [email protected]). -
Spider-Ant Associations: an Updated Review of Myrmecomorphy, Myrmecophily, and Myrmecophagy in Spiders
Hindawi Publishing Corporation Psyche Volume 2012, Article ID 151989, 23 pages doi:10.1155/2012/151989 Review Article Spider-Ant Associations: An Updated Review of Myrmecomorphy, Myrmecophily, and Myrmecophagy in Spiders Paula E. Cushing Department of Zoology, Denver Museum of Nature & Science, 2001 Colorado Boulevard, Denver, CO 80205, USA Correspondence should be addressed to Paula E. Cushing, [email protected] Received 3 October 2011; Accepted 18 December 2011 Academic Editor: Jean Paul Lachaud Copyright © 2012 Paula E. Cushing. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. This paper provides a summary of the extensive theoretical and empirical work that has been carried out in recent years testing the adaptational significance of various spider-ant associations. Hundreds of species of spiders have evolved close relationships with ants and can be classified as myrmecomorphs, myrmecophiles, or myrmecophages. Myrmecomorphs are Batesian mimics. Their close morphological and behavioral resemblance to ants confers strong survival advantages against visually hunting predators. Some species of spiders have become integrated into the ant society as myrmecophiles or symbionts. These spider myrmecophiles gain protection against their own predators, live in an environment with a stable climate, and are typically surrounded by abundant food resources. The adaptations by which this integration is made possible are poorly known, although it is hypothesized that most spider myrmecophiles are chemical mimics and some are even phoretic on their hosts. The third type of spider-ant association discussed is myrmecophagy—or predatory specialization on ants. -
The True Odor of the Odorous House Ant CLINT A
The True Odor of the Odorous House Ant CLINT A. PENICK AND ADRIAN A. SMITH ore than 13,000 ant species have been At fi rst, using scent to identify ants seems obvi- Mformally described, yet the general public ous and practical, because ants themselves com- recognizes only two main categories: red municate through smell. However, the sense of ants and black ants. Th is system has some limita- smell in humans is far less developed, and there tions, so there has been increased eff ort to provide has been recent controversy over what, exactly, additional sensory information for ant identifi ca- the odorous house ant smells like. Th is species tion, including the sense of smell. Nowhere has belongs to a large group of ants whose members this been more strongly applied than to the “odor- are thought to smell like blue cheese (Forney and ous house ant” (Tapinoma sessile Say), a common Markovetz 1971), yet numerous online sources household pest in North America that releases a report their odor as “rancid butter,” “cleaning solu- PHOTO WWW.ANTWEB.ORG FROM PHOTO curious odor when crushed (Smith 1928). tion,” or, most commonly, “rotten coconuts.” Some American Entomologist • Volume 61, Number 2 85 A. Websites B. Human Participants 100 40 80 30 60 20 40 % selected 10 20 0 0 rotten coconut blue cheese rancid butter other rotten coconut blue cheese rancid butter other Fig. 1. While 80% of websites reported the scent of the odor- Based on our chemical analysis, the major component ous house ant as “rotten coconut” (a), most participants in the of the odorous house ant scent was 6-methyl-5-hepten- smell test chose “blue cheese” (b). -
Abstract POWELL, BRADFORD EDMUND
Abstract POWELL, BRADFORD EDMUND. Interactions between the ants Linepithema humile, Tapinoma sessile and aphid mutualists. (Under the direction of Jules Silverman.) Invasive species have major impacts on the ecosystems they invade. Among the most disruptive groups of invasive species are ants. Invasive ants have caused losses in biodiversity among a wide range of taxa, including birds, mammals, lizards, but especially towards ground nesting arthropods such as native ants. Why native ants are so susceptible to invasion and how invasive ants are able to sustain massive population growth remain unclear. It has been suggested that invasive ants utilize carbohydrate resources from hemipteran exudates to fuel aggressive foraging and colony expansion. Perhaps invasive ants are simply more proficient at usurping these resources, maintaining higher hemipteran populations, etc.? I use a model invasive, the Argentine ant (Linepithema humile) and a native ant (Tapinoma sessile) to compare hemipteran tending ability and ant competition. Through a series of laboratory and field experiments I evaluated 1) sucrose consumption by individual and groups of ant workers, 2) the effect either ant species had on hemipteran population growth rates in a predator-free space, 3) the defensive ability of either ant against hemipteran predators and parasitoids, and 4) the proportion of invasive ants required to displace a native colony from a hemipteran resource. Whereas there was no difference between the species in their ability to sequester liquid resources, recruitment strategies differed considerably. Hemipteran populations in the presence of L. humile grew larger in a predator free environment and populations exposed to predators were better defended by L. humile than T. -
Chapter 7 Species-Area Relationships Are Modulated by Trophic Rank, Habitat Affinity And
PDF hosted at the Radboud Repository of the Radboud University Nijmegen The following full text is a publisher's version. For additional information about this publication click this link. http://hdl.handle.net/2066/129008 Please be advised that this information was generated on 2021-10-10 and may be subject to change. Through arthropod eyes Gaining mechanistic understanding of calcareous grassland diversity Toos van Noordwijk Through arthropod eyes Gaining mechanistic understanding of calcareous grassland diversity Van Noordwijk, C.G.E. 2014. Through arthropod eyes. Gaining mechanistic understanding of calcareous grassland diversity. Ph.D. thesis, Radboud University Nijmegen, the Netherlands. Keywords: Biodiversity, chalk grassland, dispersal tactics, conservation management, ecosystem restoration, fragmentation, grazing, insect conservation, life‑history strategies, traits. ©2014, C.G.E. van Noordwijk ISBN: 978‑90‑77522‑06‑6 Printed by: Gildeprint ‑ Enschede Lay‑out: A.M. Antheunisse Cover photos: Aart Noordam (Bijenwolf, Philanthus triangulum) Toos van Noordwijk (Laamhei) The research presented in this thesis was financially spupported by and carried out at: 1) Bargerveen Foundation, Nijmegen, the Netherlands; 2) Department of Animal Ecology and Ecophysiology, Institute for Water and Wetland Research, Radboud University Nijmegen, the Netherlands; 3) Terrestrial Ecology Unit, Ghent University, Belgium. The research was in part commissioned by the Dutch Ministry of Economic Affairs, Agriculture and Innovation as part of the O+BN program (Development and Management of Nature Quality). Financial support from Radboud University for printing this thesis is gratefully acknowledged. Through arthropod eyes Gaining mechanistic understanding of calcareous grassland diversity Proefschrift ter verkrijging van de graad van doctor aan de Radboud Universiteit Nijmegen op gezag van de rector magnificus prof.