(Hymenoptera: Formicidae) of Peru
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Ant Type Specimens (Hymenoptera, Formicidae) Deposited in the Museu De Zoologia Da Universidade De São Paulo, Brazil
Volume 48(11):75-88, 2008 Catalogue of “poneromorph” ant type specimens (Hymenoptera, Formicidae) deposited in the Museu de Zoologia da Universidade de São Paulo, Brazil Cristiane P. Scott-Santos Flávia A. Esteves Carlos Roberto F. Brandão AbsTracT The present catalogue lists the type specimes of 112 nominal “poneromorph” ant species housed in the Formicidae collection of the Hymenoptera laboratory, Museu de Zoologia da Universidade de São Paulo (MZSP). The catalogue includes types of Amblyoponinae, Ectatomminae, Heteroponerinae, Ponerinae, and Proceratiinae, that is, all poneromorph (sensu Bolton, 2003) but for the monotypic Paraponerinae, of which the collection bears no type specimens. We present here information on type categories (holotype, paratype, syntype, lectotype, and paralectotype), label data, nomenclatural changes since the original description and type specimens conservation status. At last we present indexes for the taxa names presented. Keywords: Hymenoptera, ants, types, MZSP, Amblyoponinae, Ectatomminae, Heteroponerinae, Ponerinae, Proceratiinae. INTRODucTION The purpose of the present catalogue is to pro- vide updated information on poneromorph type The Formicidae collection housed in the Hy- specimes of the MZSP collection, following Article menoptera laboratory of the Museu de Zoologia da 72 F.4 of the International Code for Zoological No- Universidade de São Paulo (MZSP) is under con- menclature (1999). struction since the end of the 19th century and is to- The poneromorph group of ants, as defined by day one of the largest and more representative ant col- Bolton (2003), is distributed worldwide and consists lections in and for the Neotropical region, as regard of circa 1,700 described species in 49 genera of six to the number of specimens, including types, and subfamilies: Amblyoponinae, Ectatomminae, Hetero- localities (Brandão, 2000). -
Differential Effects of Land Use on Ant and Herbivore Insect Communities Associated with Caryocar Brasiliense (Caryocaraceae)
Differential effects of land use on ant and herbivore insect communities associated with Caryocar brasiliense (Caryocaraceae) Frederico S. Neves1,2*, Rodrigo F. Braga1, Lucimar S. Araújo1, Ricardo I. Campos3 & Marcílio Fagundes1 1. Laboratório de Biologia da Conservação, Departamento de Biologia Geral, Universidade Estadual de Montes Claros, Montes claros, MG, Brasil; [email protected], [email protected], [email protected] 2. Laboratório de Ecologia de Insetos, Departamento de Biologia Geral, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brasil; [email protected] 3. Laboratório de Ecologia de Formigas,Universidade Federal de Viçosa, 36570-000, Viçosa, MG, Brasil; [email protected] * Corresponding author Received 03-VIII-2011. Corrected 08-II-2012. Accepted 09-III-2012. Abstract: Simplification of natural habitats leads to a modification of the community associated with a host plant. Pequi trees (Caryocar brasiliense) are common to find in central Brazil, especially in the middle of mono- cultures, such as soy, corn, pasturelands or Eucalyptus plantations. On this scenario we hypothesized that habitat modification differentially affects the diversity of ants and herbivore insects associated with this species. The aim of the work was to test if C. brasiliense trees located in human modified habitats, support a lower species richness and abundance of ants, and a greater species richness and abundance of insect herbivores, compared to preserved cerrado habitats. The study was conducted in a Cerrado area located in Northern Minas Gerais State, Brazil. Ants and herbivore insects were collected monthly during 2005 using beating technique. The results showed that ant species richness was higher in pequi trees located in preserved Cerrado, followed by trees in pastureland and Eucalyptus plantation, respectively. -
Digging Deeper Into the Ecology of Subterranean Ants: Diversity and Niche Partitioning Across Two Continents
diversity Article Digging Deeper into the Ecology of Subterranean Ants: Diversity and Niche Partitioning across Two Continents Mickal Houadria * and Florian Menzel Institute of Organismic and Molecular Evolution, Johannes-Gutenberg-University Mainz, Hanns-Dieter-Hüsch-Weg 15, 55128 Mainz, Germany; [email protected] * Correspondence: [email protected] Abstract: Soil fauna is generally understudied compared to above-ground arthropods, and ants are no exception. Here, we compared a primary and a secondary forest each on two continents using four different sampling methods. Winkler sampling, pitfalls, and four types of above- and below-ground baits (dead, crushed insects; melezitose; living termites; living mealworms/grasshoppers) were applied on four plots (4 × 4 grid points) on each site. Although less diverse than Winkler samples and pitfalls, subterranean baits provided a remarkable ant community. Our baiting system provided a large dataset to systematically quantify strata and dietary specialisation in tropical rainforest ants. Compared to above-ground baits, 10–28% of the species at subterranean baits were overall more common (or unique to) below ground, indicating a fauna that was truly specialised to this stratum. Species turnover was particularly high in the primary forests, both concerning above-ground and subterranean baits and between grid points within a site. This suggests that secondary forests are more impoverished, especially concerning their subterranean fauna. Although subterranean ants rarely displayed specific preferences for a bait type, they were in general more specialised than above-ground ants; this was true for entire communities, but also for the same species if they foraged in both strata. Citation: Houadria, M.; Menzel, F. -
Evolutionary Dynamics of Shared Niche Construction
bioRxiv preprint doi: https://doi.org/10.1101/002378; this version posted February 5, 2014. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Evolutionary dynamics of shared niche construction Philip Gerlee∗ and Alexander R.A. Anderson Integrated Mathematical Oncology, H. Lee Moffitt Cancer Center and Research Institute 12902 Magnolia Drive Tampa, FL 33612 (Dated: January 31, 2014) Many species engage in niche construction that ultimately leads to an increase in the carrying capacity of the population. We have investigated how the specificity of this behaviour affects evo- lutionary dynamics using a set of coupled logistic equations, where the carrying capacity of each genotype consists of two components: an intrinsic part and a contribution from all genotypes present in the population. The relative contribution of the two components is controlled by a specificity parameter γ, and we show that the ability of a mutant to invade a resident population depends strongly on this parameter. When the carrying capacity is intrinsic, selection is almost exclusively for mutants with higher carrying capacity, while a shared carrying capacity yields selection purely on growth rate. This result has important implications for our understanding of niche construction, in particular the evolutionary dynamics of tumor growth. In models of density-dependent growth the carrying ca- harder for other genotypes to exploit it, whereas a more pacity plays a pivotal role [1]. It represents the maximal general modification is easier to free-ride on. -
The Functions and Evolution of Social Fluid Exchange in Ant Colonies (Hymenoptera: Formicidae) Marie-Pierre Meurville & Adria C
ISSN 1997-3500 Myrmecological News myrmecologicalnews.org Myrmecol. News 31: 1-30 doi: 10.25849/myrmecol.news_031:001 13 January 2021 Review Article Trophallaxis: the functions and evolution of social fluid exchange in ant colonies (Hymenoptera: Formicidae) Marie-Pierre Meurville & Adria C. LeBoeuf Abstract Trophallaxis is a complex social fluid exchange emblematic of social insects and of ants in particular. Trophallaxis behaviors are present in approximately half of all ant genera, distributed over 11 subfamilies. Across biological life, intra- and inter-species exchanged fluids tend to occur in only the most fitness-relevant behavioral contexts, typically transmitting endogenously produced molecules adapted to exert influence on the receiver’s physiology or behavior. Despite this, many aspects of trophallaxis remain poorly understood, such as the prevalence of the different forms of trophallaxis, the components transmitted, their roles in colony physiology and how these behaviors have evolved. With this review, we define the forms of trophallaxis observed in ants and bring together current knowledge on the mechanics of trophallaxis, the contents of the fluids transmitted, the contexts in which trophallaxis occurs and the roles these behaviors play in colony life. We identify six contexts where trophallaxis occurs: nourishment, short- and long-term decision making, immune defense, social maintenance, aggression, and inoculation and maintenance of the gut microbiota. Though many ideas have been put forth on the evolution of trophallaxis, our analyses support the idea that stomodeal trophallaxis has become a fixed aspect of colony life primarily in species that drink liquid food and, further, that the adoption of this behavior was key for some lineages in establishing ecological dominance. -
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. -
Ants of the Genera Myopias and Acanthoponera.1
PSYCHE VOL. XXX. DECEMBER 1923 No. 6 ANTS OF THE GENERA MYOPIAS AND ACANTHOPONERA.1 WILLIAM MORTON WHEELER. A recent study of the Australian ants collected some years ago by Mr. A. M. Lee and myself has led me to revise the Pone- .fine genera Myopias and Acanthoponera, two groups of more than usual interest on account of their singular geographical distribution. The former genus was established by Roger more than 60 years ago for a Ceylonese ant, M. amblyops, which has not been taken since, although considerable thorough collecting has been done in India and Ceylon. A second species was brought to light in New Guinea by L. Bir6 and described in 1901 by Emery as M. cribriceps. A third species has now been discovered by Mr. Lea in Tasmania and is described in the sequel. The highly vestigial eyes in the workers of these ants show that they are subterranean in habit, but they must be extremely rare, since a total of only eleven specimens has been seen. Their recorded distribution is so discontinuous that we may regard them as vanishing relicts of forms very close to the direct ancestors of Trapeziopelta, a genus represented by a number of species in the East Indies and New Guinea. The distribution of Acanthoponera is even more interesting. It comprises two species in Australia, one in New Zealand and five in the Neotropical Region, from Chile, Argentina and Brazil to Central America and Mexico. All the American specms occur in the southern portion of the range and the forms in Central America and Mexico are merely small varieties or subspecies which have strayed beyond the optimum environ- 1Contributions from the Entomological Laboratory of the Bussey Insti- tution. -
Redalyc.A Checklist of the Ants (Hymenoptera: Formicidae) of The
Agronomía Colombiana ISSN: 0120-9965 [email protected] Universidad Nacional de Colombia Colombia Vergara-Navarro, Erika Valentina; Serna, Francisco A checklist of the ants (Hymenoptera: Formicidae) of the department of Antioquia, Colombia and new records for the country Agronomía Colombiana, vol. 31, núm. 3, 2013, pp. 324-342 Universidad Nacional de Colombia Bogotá, Colombia Available in: http://www.redalyc.org/articulo.oa?id=180329804008 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative CROP PROTECTION A checklist of the ants (Hymenoptera: Formicidae) of the department of Antioquia, Colombia and new records for the country Lista de las hormigas (Hymenoptera: Formicidae) del departamento de Antioquia, Colombia, y nuevos registros para el país Erika Valentina Vergara-Navarro1, 2 and Francisco Serna2, 3 ABSTRACT RESUMEN Antioquia is a state (department) of Colombia, located in the Antioquia es un departamento de Colombia localizado en los northwestern Andes of South America. Geologically, the north- Andes más noroccidentales de Suramérica. Geológicamente, la western region of the Western Range in Antioquia and Chocó región noroccidental de la Cordillera Occidental en Antioquia includes the fault resulting from the connection between the y Chocó contiene la falla resultante de la unión entre el Istmo Isthmus of Panamá and South America. The Occidental and de Panamá y Sudamérica. Las cordilleras Occidental y Central Central cordilleras in Colombia are characterized by a num- de Colombia se caracterizan por presentar una cantidad impor- ber of reliefs, valleys and water basins, containing historical tante de relieves, valles y cuencas hidrográficas compuestas por biological refuges and endemisms. -
Literature Cited in Lizards Natural History Database
Literature Cited in Lizards Natural History database Abdala, C. S., A. S. Quinteros, and R. E. Espinoza. 2008. Two new species of Liolaemus (Iguania: Liolaemidae) from the puna of northwestern Argentina. Herpetologica 64:458-471. Abdala, C. S., D. Baldo, R. A. Juárez, and R. E. Espinoza. 2016. The first parthenogenetic pleurodont Iguanian: a new all-female Liolaemus (Squamata: Liolaemidae) from western Argentina. Copeia 104:487-497. Abdala, C. S., J. C. Acosta, M. R. Cabrera, H. J. Villaviciencio, and J. Marinero. 2009. A new Andean Liolaemus of the L. montanus series (Squamata: Iguania: Liolaemidae) from western Argentina. South American Journal of Herpetology 4:91-102. Abdala, C. S., J. L. Acosta, J. C. Acosta, B. B. Alvarez, F. Arias, L. J. Avila, . S. M. Zalba. 2012. Categorización del estado de conservación de las lagartijas y anfisbenas de la República Argentina. Cuadernos de Herpetologia 26 (Suppl. 1):215-248. Abell, A. J. 1999. Male-female spacing patterns in the lizard, Sceloporus virgatus. Amphibia-Reptilia 20:185-194. Abts, M. L. 1987. Environment and variation in life history traits of the Chuckwalla, Sauromalus obesus. Ecological Monographs 57:215-232. Achaval, F., and A. Olmos. 2003. Anfibios y reptiles del Uruguay. Montevideo, Uruguay: Facultad de Ciencias. Achaval, F., and A. Olmos. 2007. Anfibio y reptiles del Uruguay, 3rd edn. Montevideo, Uruguay: Serie Fauna 1. Ackermann, T. 2006. Schreibers Glatkopfleguan Leiocephalus schreibersii. Munich, Germany: Natur und Tier. Ackley, J. W., P. J. Muelleman, R. E. Carter, R. W. Henderson, and R. Powell. 2009. A rapid assessment of herpetofaunal diversity in variously altered habitats on Dominica. -
Directed Aerial Descent in Canopy Ants
letters to nature responses to environmental changes that are significantly more mycorrhizae on soil aggregation depend on the interaction between plant and fungal species. New abrupt than those that would occur in nature. A Phytol. 164, 365–373 (2004). 21. Van der Heijden, M. G. A. et al. Mycorrhizal fungal diversity determines plant biodiversity, ecosystem variability and productivity. Nature 396, 69–72 (1998). Methods 22. Goverde, M., Van der Heijden, M. G. A., Wiemken, A., Sanders, I. R. & Erhardt, A. Arbuscular Each experimental unit consisted of a single plant growing in an eight-inch pot containing mycorrhizal fungi influence life history traits of a lepidopteran herbivore. Oecologia 125, 362–369 field-collected soil. Plants were initially collected as seed from the field, germinated in (2000). the laboratory and added to the experimental units as one-week-old seedlings. After each 23. Gange, A. C., Brown, V. K. & Alphin, D. M. Multitrophic links between arbuscular mycorrhizal fungi 15-week growth period, plant shoots were removed and new seedlings were added to each and insect parasitoids. Ecol. Lett. 6, 1051–1055 (2003). pot. After the first generation, the source of seed was from plants of the previous 24. Rillig, M. C. Arbuscular mycorrhizae and ecosystem processes. Ecol. Lett. 7, 740–754 (2004). generation. B. inermis is an obligate cross-pollinated plant. Some inbreeding can occur, 25. Brundrett, M. C., Piche´, Y. & Peterson, R. L. A new method for observing the morphology of vesicular- but this results in seed that is significantly smaller and distorted. Therefore only out- arbuscular mycorrhizae. Can. J. Bot. -
Sistemática Y Ecología De Las Hormigas Predadoras (Formicidae: Ponerinae) De La Argentina
UNIVERSIDAD DE BUENOS AIRES Facultad de Ciencias Exactas y Naturales Sistemática y ecología de las hormigas predadoras (Formicidae: Ponerinae) de la Argentina Tesis presentada para optar al título de Doctor de la Universidad de Buenos Aires en el área CIENCIAS BIOLÓGICAS PRISCILA ELENA HANISCH Directores de tesis: Dr. Andrew Suarez y Dr. Pablo L. Tubaro Consejero de estudios: Dr. Daniel Roccatagliata Lugar de trabajo: División de Ornitología, Museo Argentino de Ciencias Naturales “Bernardino Rivadavia” Buenos Aires, Marzo 2018 Fecha de defensa: 27 de Marzo de 2018 Sistemática y ecología de las hormigas predadoras (Formicidae: Ponerinae) de la Argentina Resumen Las hormigas son uno de los grupos de insectos más abundantes en los ecosistemas terrestres, siendo sus actividades, muy importantes para el ecosistema. En esta tesis se estudiaron de forma integral la sistemática y ecología de una subfamilia de hormigas, las ponerinas. Esta subfamilia predomina en regiones tropicales y neotropicales, estando presente en Argentina desde el norte hasta la provincia de Buenos Aires. Se utilizó un enfoque integrador, combinando análisis genéticos con morfológicos para estudiar su diversidad, en combinación con estudios ecológicos y comportamentales para estudiar la dominancia, estructura de la comunidad y posición trófica de las Ponerinas. Los resultados sugieren que la diversidad es más alta de lo que se creía, tanto por que se encontraron nuevos registros durante la colecta de nuevo material, como porque nuestros análisis sugieren la presencia de especies crípticas. Adicionalmente, demostramos que en el PN Iguazú, dos ponerinas: Dinoponera australis y Pachycondyla striata son componentes dominantes en la comunidad de hormigas. Análisis de isótopos estables revelaron que la mayoría de las Ponerinas ocupan niveles tróficos altos, con excepción de algunas especies arborícolas del género Neoponera que dependerían de néctar u otros recursos vegetales. -
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.