Hymenoptera: Formicidae
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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. -
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: Principles of Ecology, Behavioral Ecology, Human Ecology, Environmental Studies, Tropical Ecology, Biodiversity, 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. -
Ant–Fungus Species Combinations Engineer Physiological Activity Of
© 2014. Published by The Company of Biologists Ltd | The Journal of Experimental Biology (2014) 217, 2540-2547 doi:10.1242/jeb.098483 RESEARCH ARTICLE Ant–fungus species combinations engineer physiological activity of fungus gardens J. N. Seal1,2,*, M. Schiøtt3 and U. G. Mueller2 ABSTRACT such complexity, the fungus-gardening insects have evolved obligate Fungus-gardening insects are among the most complex organisms macro-symbioses with specific clades of fungi, and use fungal because of their extensive co-evolutionary histories with obligate symbionts essentially as an external digestive organ that allows the fungal symbionts and other microbes. Some fungus-gardening insect insect to thrive on otherwise non-digestible substrates, such as lineages share fungal symbionts with other members of their lineage structural carbohydrates of plants (e.g. cellulose) (Aanen et al., and thus exhibit diffuse co-evolutionary relationships, while others 2002; Aylward et al., 2012a; Aylward et al., 2012b; Bacci et al., exhibit little or no symbiont sharing, resulting in host–fungus fidelity. 1995; Farrell et al., 2001; De Fine Licht and Biedermann, 2012; The mechanisms that maintain this symbiont fidelity are currently Martin, 1987a; Mueller et al., 2005). One of the most striking unknown. Prior work suggested that derived leaf-cutting ants in the attributes of these symbioses is the degree of physiological genus Atta interact synergistically with leaf-cutter fungi (Attamyces) integration: the insect host functions as a distributor of fungal by exhibiting higher fungal growth rates and enzymatic activities than enzymes, which digest plant fibers external to the insect’s body when growing a fungus from the sister-clade to Attamyces (so-called (Aanen and Eggleton, 2005; Aylward et al., 2012b; De Fine Licht ‘Trachymyces’), grown primarily by the non-leaf cutting and Biedermann, 2012; De Fine Licht et al., 2013; Martin, 1987b; Trachymyrmex ants that form, correspondingly, the sister-clade to Schiøtt et al., 2010). -
Report on Pitfall Trapping of Ants at the Biospecies Sites in the Nature Reserve of Orange County, California
Report on Pitfall Trapping of Ants at the Biospecies Sites in the Nature Reserve of Orange County, California Prepared for: Nature Reserve of Orange County and The Irvine Co. Open Space Reserve, Trish Smith By: Krista H. Pease Robert N. Fisher US Geological Survey San Diego Field Station 5745 Kearny Villa Rd., Suite M San Diego, CA 92123 2001 2 INTRODUCTION: In conjunction with ongoing biospecies richness monitoring at the Nature Reserve of Orange County (NROC), ant sampling began in October 1999. We quantitatively sampled for all ant species in the central and coastal portions of NROC at long-term study sites. Ant pitfall traps (Majer 1978) were used at current reptile and amphibian pitfall trap sites, and samples were collected and analyzed from winter 1999, summer 2000, and winter 2000. Summer 2001 samples were recently retrieved, and are presently being identified. Ants serve many roles on different ecosystem levels, and can serve as sensitive indicators of change for a variety of factors. Data gathered from these samples provide the beginning of three years of baseline data, on which long-term land management plans can be based. MONITORING OBJECTIVES: The California Floristic Province, which includes southern California, is considered one of the 25 global biodiversity hotspots (Myers et al. 2000). The habitat of this region is rapidly changing due to pressure from urban and agricultural development. The Scientific Review Panel of the State of California's Natural Community Conservation Planning Program (NCCP) has identified preserve design parameters as one of the six basic research needs for making informed long term conservation planning decisions. -
Evidence for a Thoracic Crop in the Workers of Some Neotropical Pheidole Species (Formicidae: Myrmicinae)
Arthropod Structure & Development 59 (2020) 100977 Contents lists available at ScienceDirect Arthropod Structure & Development journal homepage: www.elsevier.com/locate/asd Evidence for a thoracic crop in the workers of some Neotropical Pheidole species (Formicidae: Myrmicinae) * A. Casadei-Ferreira a, , G. Fischer b, E.P. Economo b a Departamento de Zoologia, Universidade Federal do Parana, Avenida Francisco Heraclito dos Santos, s/n, Centro Politecnico, Curitiba, Mailbox 19020, CEP 81531-980, Brazil b Biodiversity and Biocomplexity Unit, Okinawa Institute of Science and Technology Graduate University, 1919-1 Tancha, Onna, Okinawa, 904-0495, Japan article info abstract Article history: The ability of ant colonies to transport, store, and distribute food resources through trophallaxis is a key Received 28 May 2020 advantage of social life. Nonetheless, how the structure of the digestive system has adapted across the Accepted 21 July 2020 ant phylogeny to facilitate these abilities is still not well understood. The crop and proventriculus, Available online xxx structures in the ant foregut (stomodeum), have received most attention for their roles in trophallaxis. However, potential roles of the esophagus have not been as well studied. Here, we report for the first Keywords: time the presence of an auxiliary thoracic crop in Pheidole aberrans and Pheidole deima using X-ray micro- Ants computed tomography and 3D segmentation. Additionally, we describe morphological modifications Dimorphism Mesosomal crop involving the endo- and exoskeleton that are associated with the presence of the thoracic crop. Our Liquid food results indicate that the presence of a thoracic crop in major workers suggests their potential role as Species group repletes or live food reservoirs, expanding the possibilities of tasks assumed by these individuals in the colony. -
Thievery in Rainforest Fungus-Growing Ants: Interspecific Assault on Culturing Material at Nest Entrance
Insectes Sociaux (2018) 65:507–510 https://doi.org/10.1007/s00040-018-0632-9 Insectes Sociaux SHORT COMMUNICATION Thievery in rainforest fungus-growing ants: interspecific assault on culturing material at nest entrance M. U. V. Ronque1 · G. H. Migliorini2 · P. S. Oliveira3 Received: 15 March 2018 / Revised: 21 May 2018 / Accepted: 22 May 2018 / Published online: 5 June 2018 © International Union for the Study of Social Insects (IUSSI) 2018 Abstract Cleptobiosis in social insects refers to a relationship in which members of a species rob food resources, or other valuable items, from members of the same or a different species. Here, we report and document in field videos the first case of clepto- biosis in fungus-growing ants (Atta group) from a coastal, Brazilian Atlantic rainforest. Workers of Mycetarotes parallelus roam near the nest and foraging paths of Mycetophylax morschi and attack loaded returning foragers of M. morschi, from which they rob cultivating material for the fungus garden. Typically, a robbing Mycetarotes stops a loaded returning Myce- tophylax, vigorously pulls away the fecal item from the forager’s mandibles, and brings the robbed item to its nearby nest. In our observations, all robbed items consisted of arthropod feces, the most common culturing material used by M. parallelus. Robbing behavior is considered a form of interference action to obtain essential resources needed by ant colonies to cultivate the symbiont fungus. Cleptobiosis between fungus-growing ants may increase colony contamination, affect foraging and intracolonial behavior, as well as associated microbiota, with possible effects on the symbiont fungus. The long-term effects of this unusual behavior, and associated costs and benefits for the species involved, clearly deserve further investigation. -
Comprehensive Phylogeny of Myrmecocystus Honey Ants Highlights Cryptic Diversity and Infers Evolution During Aridification of the American Southwest
Molecular Phylogenetics and Evolution 155 (2021) 107036 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Comprehensive phylogeny of Myrmecocystus honey ants highlights cryptic diversity and infers evolution during aridification of the American Southwest Tobias van Elst a,b,*, Ti H. Eriksson c,d, Jürgen Gadau a, Robert A. Johnson c, Christian Rabeling c, Jesse E. Taylor c, Marek L. Borowiec c,e,f,* a Institute for Evolution and Biodiversity, University of Münster, Hüfferstraße 1, 48149 Münster, Germany b Institute of Zoology, University of Veterinary Medicine Hannover, Bünteweg 17, 30559 Hannover, Germany c School of Life Sciences, Arizona State University, 427 E Tyler Mall, Tempe, AZ 85287-1501, USA d Beta Hatch Inc., 200 Titchenal Road, Cashmere, WA 98815, USA e Department of Entomology, Plant Pathology and Nematology, University of Idaho, 875 Perimeter Drive, Moscow, ID 83844-2329, USA f Institute for Bioinformatics and Evolutionary Studies (IBEST), University of Idaho, 875 Perimeter Drive, Moscow, ID 83844-2329, USA ARTICLE INFO ABSTRACT Keywords: The New World ant genus Myrmecocystus Wesmael, 1838 (Formicidae: Formicinae: Lasiini) is endemic to arid Cryptic diversity and semi-arid habitats of the western United States and Mexico. Several intriguing life history traits have been Formicidae described for the genus, the best-known of which are replete workers, that store liquified food in their largely Molecular Systematics expanded crops and are colloquially referred to as “honeypots”. Despite their interesting biology and ecological Myrmecocystus importance for arid ecosystems, the evolutionary history of Myrmecocystus ants is largely unknown and the Phylogenomics Ultraconserved elements current taxonomy presents an unsatisfactory systematic framework. -
Rachel Raudenbush
Nathan E. Smith PhD Candidate - Arizona State University – School of Life Sciences EDUCATION Arizona State University Tempe, AZ August 2013-present Animal Behavior PhD student GPA: 4.0 Juniata College Huntingdon, Pennsylvania May 2013 Bachelor of Science Major: Biology Minor: Anthropology GPA: 3.93 Summa cum laude with Honors in biology RESEARCH EXPERIENCES PhD Candidate- Arizona State University Fall 2013-Present Dissertation: Macronutrient Regulation by the Desert Leafcutter Ant Acromyrmex versicolor Research Assistant- Dr. Peter Dedon, MIT Summer 2012 Genomic Mapping of DNA Damage Research Assistant- Dr. Jill Keeney, Juniata College Spring 2011-Spring 2013 Identifying the role of an orphan gene in the mechanism of retrotransposition in yeast Research Assistant- Dr. Norris Muth, Juniata College Spring 2010-Fall 2010 Plant community restoration after mortality of an invasive species AWARDS Social Insect Research Group Student Grant ($1000) Fall 2018 School of Life Sciences Travel Award ($400) Summer 2018, Summer 2017, Fall 2016 School of Life Sciences RTI Graduate Fieldwork Award ($2000) Spring 2017 School of Life Sciences RTI Graduate Fieldwork Award ($1500) Spring 2016 School of Life Sciences Graduate Research Scholarship ($3500) Summer 2015 School of Life Sciences Graduate Research Scholarship ($4000) Summer 2014 The Brumbaugh Science Prize for academic achievement, Juniata College ($500) Spring 2013 The William A. Schlicter Award for academic achievement and character, Juniata College ($500) Spring 2013 Dr. Homer & Ethel Will Endowed Scholarship Fund in Biology, Juniata College ($150) Spring 2012 VonLiebig Student Research Fellowship, Juniata College ($2000) Summer 2010 Robert C. Byrd Scholarship ($1500) Summer 2009 MEMBERSHIPS Animal Behavior Society International Union for the Study of Social Insects Entomological Society of America βββ, National Biological Honor Society Juniata College Honors Society PUBLICATIONS Patrick T. -
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. -
Hybridization in Ants
Rockefeller University Digital Commons @ RU Student Theses and Dissertations 2020 Hybridization in Ants Ian Butler Follow this and additional works at: https://digitalcommons.rockefeller.edu/ student_theses_and_dissertations Part of the Life Sciences Commons HYBRIDIZATION IN ANTS A Thesis Presented to the Faculty of The Rockefeller University in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy by Ian Butler June 2020 © Copyright by Ian Butler 2020 HYBRIDIZATION IN ANTS Ian Butler, Ph.D. The Rockefeller University 2020 Interspecific hybridization is a relatively common occurrence within all animal groups. Two main factors make hybridization act differently in ants than in other species: eusociality and haplodiploidy. These factors serve to reduce the costs of interspecific hybridization in ants while simultaneously allowing them to take advantage of certain benefits. Eusociality may mitigate the effects of hybridization by allowing hybrids to be shunted into the worker caste, potentially reducing the effects of hybrid sterility. In haplodiploid species, males do not have a father. They instead develop from unfertilized eggs as haploid clones of their mother. This means that interspecifically mated queens do not completely sacrifice reproductive potential even if all hybrids are sterile because they can still produce fertile males. These factors in turn suggest that hybridization should be more common among the social Hymenoptera than other animal groups. Nevertheless, current data suggest that ants hybridize at rates similar to other animal groups, although these data are limited. Furthermore, there is a large amount of overlap between cases of interspecific hybridization and cases of genetic caste determination. A majority of the cases in ants where caste is determined primarily by genotype are associated with hybridization. -
Foraging Ecology of the Desert Leaf-Cutting Ant, Acromyrmex Versicolor, in Arizona (Hymenoptera: Formicidae)
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/256979550 Foraging ecology of the desert leaf-cutting ant, Acromyrmex versicolor, in Arizona (Hymenoptera: Formicidae) Article in Sociobiology · January 2001 CITATIONS READS 13 590 3 authors, including: James K. Wetterer Florida Atlantic University 184 PUBLICATIONS 3,058 CITATIONS SEE PROFILE Some of the authors of this publication are also working on these related projects: Ant stuff View project Systematics and Evolution of the Tapinoma ants (Formicidae: Dolichoderinae) from the Neotropical region View project All content following this page was uploaded by James K. Wetterer on 17 May 2014. The user has requested enhancement of the downloaded file. 1 Foraging Ecology of the Desert Leaf-Cutting Ant, Acromyrmex versicolor, in Arizona (Hymenoptera: Formicidae) by James K. Wetterer1,2, Anna G. Himler1, & Matt M. Yospin1 ABSTRACT The desert would seem to be an inhospitable place for leaf-cutting ants (Acromyrmex spp. and Atta spp.), both because the leaves of desert perennials are notably well-defended, both chemically and physically, and because leaf-cutters grow a fungus that requires constant high humidity. We investigated strategies that leaf-cutters use to survive in arid environments by examining foraging activity, resource use, forager size, load size, and nesting ecology of the desert leaf-cutting ant, Acromyrmex versicolor, at 12 colonies from 6 sites in Arizona during June, August, and November 1997, and March 1998. The ants showed striking seasonal changes in materials harvested, apparently in response to changes in the availability of preferred resources. Acromyrmex versicolor foragers (n = 800) most commonly collected dry vegetation (54.3% of all loads), but also harvested ephem- eral resources, such as dry flowers (18.6%), fresh young leaves (18.5%), fruits and seeds (4.0%), and fresh flowers (3.5%), when seasonally available. -
Acromyrmex Versicolor, Myrmecocystus Mimicus and Messor Per- Gandei
COLONY FOUNDING BEHAVIOR OF SOME DESERT ANTS: GEOGRAPHIC VARIATION IN METROSIS BY STEVEN W. RISSING 1, ROBERT A. JOHNSON2, AND JOHN W. MARTIN3 Social Insect Research Group, Department of Biology, Arizona State University, Tempe, AZ 85287-1501; Current Address: Department of Evolution, Ecology and Organismal Biology, The Ohio State University, Columbus, OH 43210. 2 Social Insect Research Group, Department of Biology, Arizona State University, Tempe, AZ 85287-1501. P.O. Box 458, Dolan Springs, AZ 86441. ABSTRACT The ants Pogonomyrmex californicus and Pheidole tucsonica display cooperative colony foundation with co-foundresses form- ing associations without respect to relatedness. Geographic varia- tion in method of colony foundation [cooperative (pleometrosis) versus non-cooperative (haplometrosis)] occurs in P. californicus, Acromyrmex versicolor, Myrmecocystus mimicus and Messor per- gandei. Such variation in colony founding behavior strongly sug- gests that comparative studies of the adaptive value of cooperative colony founding will be extremely rewarding. INTRODUCTION W. M. Wheeler (1910) believed firmly that, in the vast majority of ant species, new colonies are founded by solitary queens (hap- lometrosis) and retain a single queen throughout the colony life- time (monogyny). This conception was assumed to be generally true until publication of a seminal paper by H611dobler and Wilson (1977). These authors drew attention to the frequent occurrence of multiple fertile queens in mature colonies (polygyny) and identi- fied several species in which multiple founding queens cooperate to start new colonies (pleometrosis). While the number of ant Manuscript received 18 July 1996. 95 96 Psyche [Vol. 103 species displaying cooperative colony foundation has grown steadily (Rissing and Pollock 1988), the discovery and documenta- tion of intraspecific geographical variation in pleometrosis is new and little explored (see Ryti 1988).