Mycocepurus goeldii

Mycocepurus goeldii
Scientific classification
Kingdom:	Animalia
Phylum:	Arthropoda
Class:	Insecta
Order:	Hymenoptera
Family:	Formicidae
Subfamily:	Myrmicinae
Tribe:	Attini
Genus:	Mycocepurus
Species:	M. goeldii
Binomial name
Mycocepurus goeldii (Forel, 1893) Specimen labels
Synonyms
Atta goeldii schuppi Forel, 1901 Descolemyrma ogloblini Kusnezov, 1951 Mycocepurus goeldii gentilis Santschi, 1925 Mycocepurus ogloblini Santschi, 1933

Distribution

Ranging approximately from the 40th to the 67th meridian west and from the 2nd to the 31st latitude south, an area covering most of Brazil, parts of Bolivia, Paraguay and northern Argentina.

Latitudinal Distribution Pattern

Latitudinal Range: -1.76556° to -64.36°.

North Temperate	North Subtropical	Tropical	South Subtropical	South Temperate

• Source: AntMaps

Distribution based on Regional Taxon Lists

Neotropical Region: Argentina, Brazil (type locality), Guyana, Paraguay.

Distribution based on AntMaps

Distribution based on AntWeb specimens

Check data from AntWeb

Countries Occupied

Number of countries occupied by this species based on AntWiki Regional Taxon Lists. In general, fewer countries occupied indicates a narrower range, while more countries indicates a more widespread species.

Estimated Abundance

Relative abundance based on number of AntMaps records per species (this species within the purple bar). Fewer records (to the left) indicates a less abundant/encountered species while more records (to the right) indicates more abundant/encountered species.

Habitat

The range of habitats occupied by M. goeldii is remarkably diverse and ranges from Amazon rainforest, savannahs (Cerrado) to the fertile South American lowlands (Pampas), and secondary habitats disturbed by human activities. It does not occur in elevated sites of the South American Cordilleras.

Abundance

Abundant and conspicuous.

Biology

Explore Fungus Growing  For additional details see Fungus growing ants. A handful of ant species (approx. 275 out of the known 15,000 species) have developed the ability to cultivate fungus within their nests. In most species the fungus is used as the sole food source for the larvae and is an important resource for the adults as well. Additionally, in a limited number of cases, the fungus is used to construct part of the nest structure but is not as a food source. These fungus-feeding species are limited to North and South America, extending from the pine barrens of New Jersey, United States, in the north (Trachymyrmex septentrionalis) to the cold deserts in Argentina in the south (several species of Acromyrmex). Species that use fungi in nest construction are known from Europe and Africa (a few species in the genera Crematogaster, Lasius). The details of fungal cultivation are rich and complex. First, a wide variety of materials are used as substrate for fungus cultivating. The so-called lower genera include species that prefer dead vegetation, seeds, flowers, fruits, insect corpses, and feces, which are collected in the vicinity of their nests. The higher genera include non leaf-cutting species that collect mostly fallen leaflets, fruit, and flowers, as well as the leafcutters that collect fresh leaves from shrubs and trees. Second, while the majority of fungi that are farmed by fungus-feeding ants belong to the family Lepiotaceae, mostly the genera Leucoagaricus and Leucocoprinus, other fungi are also involved. Some species utilise fungi in the family Tricholomataceae while a few others cultivate yeast. The fungi used by the higher genera no longer produce spores. Their fungi produce nutritious and swollen hyphal tips (gongylidia) that grow in bundles called staphylae, to specifically feed the ants. Finally, colony size varies tremendously among these ants. Lower taxa mostly live in inconspicuous nests with 100–1000 individuals and relatively small fungus gardens. Higher taxa, in contrast, live in colonies made of 5–10 million ants that live and work within hundreds of interconnected fungus-bearing chambers in huge subterranean nests. Some colonies are so large, they can be seen from satellite photos, measuring up to 600 m3. Based on these habits, and taking phylogenetic information into consideration, these ants can be divided into six biologically distinct agricultural systems (with a list of genera involved in each category): Nest Construction A limited number of species that use fungi in the construction of their nests. some Crematogaster some Lasius Lower Agriculture Practiced by species in the majority of fungus-feeding genera, including those thought to retain more primitive features, which cultivate a wide range of fungal species in the tribe Leucocoprineae. some Apterostigma Cyatta (1 species) some Cyphomyrmex Kalathomyrmex (1 species) Mycocepurus (6 species) Myrmicocrypta (31 species) Mycetarotes (4 species) Mycetosoritis (2 species) Mycetophylax (21 species) Paramycetophylax (1 species) Xerolitor (1 species) Coral Fungus Agriculture Practiced by species in the Apterostigma pilosum species-group, which cultivate fungi within the Pterulaceae. some Apterostigma Yeast Agriculture Practiced by species within the Cyphomyrmex rimosus species-group, which cultivate a distinct clade of leucocoprineaceous fungi derived from the lower attine fungi. some Cyphomyrmex Generalized Higher Agriculture Practiced by species in several genera of non-leaf-cutting "higher attine" ants, which cultivate a distinct clade of leucocoprineaceous fungi separately derived from the lower attine fungi. Mycetomoellerius (31 species) Paratrachymyrmex (9 species) Sericomyrmex (11 species) Trachymyrmex (9 species) Leaf-Cutter Agriculture A subdivision of higher attine agriculture practiced by species within several ecologically dominant genera, which cultivate a single highly derived species of higher attine fungus. Acromyrmex (56 species) Amoimyrmex (3 species) Atta (20 species) Note that the farming habits of Mycetagroicus (4 species) are unknown. Also, while species of Pseudoatta (2 species) are closely related to the fungus-feeding genus Acromyrmex, they are social parasites, living in the nests of their hosts and are not actively involved in fungus growing. ‎

Rabeling & Bacci (2010) - Mycocepurus goeldii is a conspicuous, widely distributed species. The natural history of Mycocepurus goeldii has been studied near Sao Paulo City (Luederwaldt, 1918, 1926) and in the Manaus region of the Amazon Basin (Rabeling et al., 2007b).

A queen of Mycocepurus castrator standing on a host Mycocepurus goeldii queen.

In Rio Claro, Sao Paulo State, Brazil Mycocepurus goeldii is parasitized by Mycocepurus castrator.

Colony Attributes

A natural history study of M. goeldii in the Amazon Basin (Rabeling et al., 2007b) showed that some colonies had a single queen, whereas others were occupied by as many as four queens. Dissection of eight individuals from three separate colonies revealed that all of them were inseminated and had fully developed ovaries, demonstrating that these colonies were functionally polygynous. A M. goeldii colony studied in 2008 contained a single reproductively active queen, 33 alate queens, 496 workers and no males. During the excavation, males and queens were leaving the maternal colony for their nuptial flight, which started on 7 October.

Castes

M. goeldii queen (b,d,f,h)

M. goeldii male (b,d,f,h)

Nomenclature

The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.

• goeldii. Atta (Mycocepurus) goeldii Forel, 1893g: 370 (footnote) (w.) BRAZIL. Forel, 1908c: 353 (q.m.). Combination in Mycocepurus: Luederwaldt, 1918: 39. Senior synonym of gentilis, ogloblini Santschi, ogloblini Kusnezov, schuppi: Kempf, 1963b: 420.
• schuppi. Atta (Mycocepurus) goeldii var. schuppi Forel, 1901d: 301 (w.) BRAZIL. Combination in Mycocepurus: Emery, 1924d: 335. Junior synonym of goeldii: Kempf, 1963b: 420.
• gentilis. Mycocepurus goeldii st. gentilis Santschi, 1925b: 17 (w.) BRAZIL. Junior synonym of goeldii: Kempf, 1963b: 420.
• ogloblini. Mycocepurus ogloblini Santschi, 1933e: 119, figs. 12, 13 (w.q.) ARGENTINA. Junior synonym of goeldii: Kempf, 1963b: 420.
• ogloblini. Descolemyrma ogloblini Kusnezov, 1951d: 460, pl. 1, fig. 1 (m.) ARGENTINA. [Unresolved junior secondary homonym of ogloblini Santschi, above.] Junior synonym of goeldii: Kempf, 1963b: 420.

Description

Karyotype

• See additional details at the Ant Chromosome Database.

 Explore: Show all Karyotype data or Search these data. See also a list of all data tables or learn how data is managed.

• 2n = 8, karyotype = 8M (Brazil) (Barros et al., 2010).
• n = 4, 2n = 8, karyotype = 4M+4SM (Brazil) (Cardoso & Cristiano, 2021).

References

• Albuquerque, E., Prado, L., Andrade-Silva, J., Siqueira, E., Sampaio, K., Alves, D., Brandão, C., Andrade, P., Feitosa, R., Koch, E., Delabie, J., Fernandes, I., Baccaro, F., Souza, J., Almeida, R., Silva, R. 2021. Ants of the State of Pará, Brazil: a historical and comprehensive dataset of a key biodiversity hotspot in the Amazon Basin. Zootaxa 5001, 1–83 (doi:10.11646/zootaxa.5001.1.1).
• Apolinário, L.da C.M.H., Almeida, Â.A.de, Queiroz, J.M., Vargas, A.B., Almeida, F.S. 2019. Diversity and guilds of ants in different land-use Systems in Rio de Janeiro State, Brazil. Floresta e Ambiente 26, e20171152 (doi:10.1590/2179-8087.115217).
• Baer, B. 2011. The copulation biology of ants (Hymenoptera: Formicidae). Myrmecological News 14: 55-68.
• Barcoto, M.O., Carlos-Shanley, C., Fan, H., Ferro, M., Nagamoto, N.S., Bacci, M., Currie, C.R., Rodrigues, A. 2020. Fungus-growing insects host a distinctive microbiota apparently adapted to the fungiculture environment. Scientific Reports 10: 12384 (doi:10.1038/S41598-020-68448-7).
• Barros, L.A.C., Rabeling, C., Teixeira, G.A., dos Santos Ferreira Mariano, C., Delabie, J. H. C., de Aguiar, H. J. A. C. 2022. Decay of homologous chromosome pairs and discovery of males in the thelytokous fungus-growing ant Mycocepurus smithii. Scientific Reports 12, 4860 (doi:10.1038/s41598-022-08537-x).
• Calazans, E.G., Costa, F.V.da, Cristiano, M.P., Cardoso, D.C. 2020. Daily dynamics of an ant community in a mountaintop ecosystem. Environmental Entomology 49, 383–390 (doi:10.1093/ee/nvaa011).
• Cardoso, D. C., Cristiano, M. P. 2021. Karyotype diversity, mode, and tempo of the chromosomal evolution of Attina (Formicidae: Myrmicinae: Attini): Is there an upper limit to chromosome number? Insects 1212, 1084 (doi:10.3390/insects12121084).
• Correia, J.P.S.O., Mariano, C S F., Delabie, J.H.C., Lacau, S., Costa, M.A. 2016. Cytogenetic analysis of Pseudoponera stigma and Pseudoponera gilberti (Hymenoptera: Formicidae: Ponerinae): a taxonomic approach. Florida Entomologist 99: 718-721.
• de la Mora, A., Sankovitz, M., Purcell, J. 2020. Ants (Hymenoptera: Formicidae) as host and intruder: recent advances and future directions in the study of exploitative strategies. Myrmecological News 30: 53-71 (doi:10.25849/MYRMECOL.NEWS_030:053).
• Forel, A. 1893j. Formicides de l'Antille St. Vincent, récoltées par Mons. H. H. Smith. Trans. Entomol. Soc. Lond. 1893: 333-418 (page 370, (footnote) worker described)
• Forel, A. 1908h. Ameisen aus Sao Paulo (Brasilien), Paraguay etc. gesammelt von Prof. Herm. v. Ihering, Dr. Lutz, Dr. Fiebrig, etc. Verh. K-K. Zool.-Bot. Ges. Wien 58: 340-418 (page 353, queen, male described)
• Kempf, W. W. 1963b. A review of the ant genus Mycocepurus Forel, 1893 (Hymenoptera: Formicidae). Stud. Entomol. 6: 417-432 (page 420, Senior synonym of gentilis, ogloblini Santschi, ogloblini Kusnezov, schuppi)
• Leal, I. R., P. S. D. Silva, and P. S. Oliveira. 2011. Natural History and Ecological Correlates of Fungus-Growing Ants (Formicidae: Attini) in the Neotropical Cerrado Savanna. Annals of the Entomological Society of America. 104:901-908. doi:10.1603/an11067
• Luederwaldt, H. 1918. Notas myrmecologicas. Rev. Mus. Paul. 10: 29-64 (page 39, Combination in Mycocepurus)
• Luísa Antônia Campos Barros, Hilton Jeferson Alves Cardoso de Aguiar, Cléa dos Santos Ferreira Mariano, Jacques Hubert Charles Delabie & Silvia das Graças Pompolo. 2010. Cytogenetic Characterization of the Lower-Attine Mycocepurus goeldii (Formicidae: Myrmicinae: Attini). Sociobiology 56(1): 57-66.
• Lutinski, J., de Filtro, M., Baucke, L., Dorneles, F., Lutinski, C., Guarda, C. 2021. Ant assemblages (Hymenoptera: Formicidae) from areas under the direct influence of two small hydropower plants in Brazil. Brazilian Journal of Environmental Sciences (Online), 1-9 (doi:10.5327/Z217694781030).
• Melo, T.S., Koch, E.B.A., Andrade, A.R.S., Travassos, M.L.O., Peres, M.C.L., Delabie, J.H.C. 2021. Ants (Hymenoptera: Formicidae) in different green areas in the metropolitan region of Salvador, Bahia state, Brazil. Brazilian Journal of Biology 82, e236269 (doi:10.1590/1519-6984.236269).
• Menegatti, C., Fukuda, T.T.H., Pupo, M.T. 2020. Chemical ecology in insect-microbe interactions in the Neotropics. Planta Medica, a-1229–9435. (doi:10.1055/a-1229-9435).
• Moleiro, H.R., Da Silva-Melo, A., Giannotti, E. 2021. Nest architecture and animals associated with Neoponera verenae (Forel) (Formicidae, Ponerinae). Sociobiology 68, e6246 (doi:10.13102/sociobiology.v68i3.6246).
• Moura, M.N., Cardoso, D.C., Cristiano, M.P. 2020. The tight genome size of ants: diversity and evolution under ancestral state reconstruction and base composition. Zoological Journal of the Linnean Society, zlaa135 (doi:10.1093/zoolinnean/zlaa135).
• Rabeling, C. 2020. Social Parasitism. In: Starr, C. (ed.) Encyclopedia of Social Insects. Springer, Cham. (doi:10.1007/978-3-319-90306-4_175-1).
• Rabeling, C. and Bacci M. 2010. A new workerless inquiline in the Lower Attini (Hymenoptera: Formicidae), with a discussion of social parasitism in fungus-growing ants. Systematic Entomology. 35:379-392.
• Rabeling, C., Schultz, T.R., Pierce, N.E., Bacci, M. 2014. A social parasite evolved reproductive isolation from its fungus-growing ant host in sympatry. Current Biology 24, 2047–2052 (doi:10.1016/J.CUB.2014.07.048).
• Rabeling, C., Verhaagh, M. & Engels, W. 2007. Comparative study of nest architecture and colony structure of the fungus-growing ants, Mycocepurus goeldii and M. smithii. Journal of Insect Science 7, Article 40.
• Tibcherani, M., Aranda, R., Mello, R.L. 2020. Time to go home: The temporal threshold in the regeneration of the ant community in the Brazilian savanna. Applied Soil Ecology 150, 103451 (doi:10.1016/j.apsoil.2019.103451).

References based on Global Ant Biodiversity Informatics

• Battirola, L.E., M.I. Marques, J. Adis and J.H.C. Delabie. 2005. Composicao da comunidade de Formicidae (Insecta, Hymenoptera) em copas de Attalea phalerata Mart. Composic?a?o da comunidade de Formicidae (Insecta, Hymenoptera) em copas de Attalea phalerata Mart. (Arecaceae), no Pantanal de Pocone?, Mato Grosso, Brasil. Revista Brasileira de Entomologia 49(1): 107-117.
• Boscardin J., J. Garlet, and E. Correa Costa. 2012. Mirmecofauna epigéica (Hymenoptera: Formicidae) em plantios de Eucalyptus spp. (Myrtales: Myrtaceae) na região oeste do estado do Rio Grande do Sul, Brasil. Entomotropica 27(3): 119-128.
• Brandao, C.R.F. 1991. Adendos ao catalogo abreviado das formigas da regiao neotropical (Hymenoptera: Formicidae). Rev. Bras. Entomol. 35: 319-412.
• Caldart V. M., S. Iop, J. A. Lutinski, and F. R. Mello Garcia. 2012. Ants diversity (Hymenoptera, Formicidae) of the urban perimeter of Chapecó county, Santa Catarina, Brazil. Revista Brasileira de Zoociências 14 (1, 2, 3): 81-94.
• Campos Barros L. A., H. J. Alves Cardoso de Aguiar, C. dos Santos Ferreira Mariano, J. H. C. Delabie, and S. das Graças Pompolo. 2010. Cytogenetic Characterization of the Lower-Attine Mycocepurus goeldii (Formicidae: Myrmicinae: Attini). Sociobiology 56(1): 57-66.
• Christianini A. V., A. J. Mayhé-Nunes, and P. S. Oliveira. 2012. Exploitation of Fallen Diaspores By Ants: Are There Ant-Plant Partner Choices? Biotropica 44: 360-367.
• Christianini A. V., and P. S. Oliveira. 2009. The relevance of ants as seed rescuers of a primarily bird-dispersed tree in the neotropical cerrado savanna. Oecologia 160: 735–745.
• Clemes Cardoso D., M. Passos Cristiano, J. Heinze, and M. G. Tavares. 2014. A nuclear DNA based phylogeny of endemic sand dune ants of the genus Mycetophylax (Emery, 1913): How morphology is reflected in molecular data. Molecular phylogenetics and Evolution 70: 378–382.
• Costa-Milanez C. B., G. Lourenco-Silva, P. T. A. Castro, J. D. Majer, and S. P. Ribeiro. 2014. Are ant assemblages of Brazilian veredas characterised by location or habitat type? Braz. J. Biol. 74(1): 89-99.
• Cuezzo, F. 1998. Formicidae. Chapter 42 in Morrone J.J., and S. Coscaron (dirs) Biodiversidad de artropodos argentinos: una perspectiva biotaxonomica Ediciones Sur, La Plata. Pages 452-462.
• Dattilo W., N. Sibinel, J. C. F. Falcao, and R. V. Nunes. 2011. Ant fauna in a urban remnant of Atlantic forest in the municipuality of Marilia, state of Sao Paulo, Brazil. Bioscience Journal 27(3): 494-504.
• Dias N. S., R. Zanetti, M. S. Santos, J. Louzada, and J. H. C. Delabie. 2008. Interaction between forest fragments and adjacent coffee and pasture agroecosystems: responses of the ant communities (Hymenoptera, Formicidae). Iheringia, Sér. Zool., Porto Alegre, 98(1): 136-142.
• Favretto M. A., E. Bortolon dos Santos, and C. J. Geuster. 2013. Entomofauna from West of Santa Catarina State, South of Brazil. EntomoBrasilis 6 (1): 42-63.
• Fernandes I., and J. de Souza. 2018. Dataset of long-term monitoring of ground-dwelling ants (Hymenoptera: Formicidae) in the influence areas of a hydroelectric power plant on the Madeira River in the Amazon Basin. Biodiversity Data Journal 6: e24375.
• Fernandes W. D., D. Lange, and S. de Almeida Soares. 2010. Communities of ants (Hymenoptera: Formicidae) in fragmented environments. Sociobiology 55(1B): 255-271.
• Fernández, F. and S. Sendoya. 2004. Lista de las hormigas neotropicales. Biota Colombiana Volume 5, Number 1.
• Forel A. 1908. Ameisen aus Sao Paulo (Brasilien), Paraguay etc. gesammelt von Prof. Herm. v. Ihering, Dr. Lutz, Dr. Fiebrig, etc. Verhandlungen der Kaiserlich-Königlichen Zoologisch-Botanischen Gesellschaft in Wien 58: 340-418.
• Forel A. 1911. Ameisen des Herrn Prof. v. Ihering aus Brasilien (Sao Paulo usw.) nebst einigen anderen aus Südamerika und Afrika (Hym.). Deutsche Entomologische Zeitschrift 1911: 285-312.
• Gallego-Ropero M.C., R.M. Feitosa & J.R. Pujol-Luz, 2013. Formigas (Hymenoptera, Formicidae) Associadas a Ninhos de Cornitermes cumulans Kollar (Isoptera, Termitidae) no Cerrado do Planalto Central do Brasil. EntomoBrasilis, 6(1): 97-101.
• Ilha C., J. A. Lutinski, D. Von Muller Pereira, F. R. Mello Garcia. 2009. Riqueza de formigas (Hymenoptera: Formicidae) de Bacia da Sanga Caramuru, municipio de Chapeco-SC. Biotemas 22(4): 95-105.
• Iop S., V. M. Caldart, J. A. Lutinski, and F. R. Mello Garcia. 2009. Formigas urbanas da cidade de Xanxerê, Santa Catarina, Brasil. Biotemas 22(2): 55-64.
• Kamura, C.M., M.S.C. Morini, C.J. Figueiredo, O.C. Bueno, and A.E.C. Campos-Farinha. 2007. Comunidades de formigas (Hymenoptera: Formicidae) em um ecossistema urbano próximo à Mata Atlântica. Brazilian Journal of Biology 67(4): 635-641
• Kempf W. W. 1963. A review of the ant genus Mycocepurus Forel, 1893 (Hymenoptera: Formicidae). Studia Entomologica 6: 417-432.
• Kempf, W.W. 1972. Catalago abreviado das formigas da regiao Neotropical (Hym. Formicidae) Studia Entomologica 15(1-4).
• Klingenberg, C. and C.R.F. Brandao. 2005. The type specimens of fungus growing ants, Attini (Hymenoptera, Formicidae, Myrmicinae) deposited in the Museu de Zoologia da Universidade de Sao Paulo, Brazil. Papeis Avulsos de Zoologia 45(4):41-50
• Kusnezov N. 1951. Descolemyrma ogloblini, género y especie nuevos de la tribu Attini (Hymenoptera, Formicidae). Acta Zoologica Lilloana 11: 459-465.
• Kusnezov N. 1978. Hormigas argentinas: clave para su identificación. Miscelánea. Instituto Miguel Lillo 61:1-147 + 28 pl.
• Leal, I.R. and P.S. Oliveira. 2000. Foraging ecology of attine ants in a Neotropical savanna: seasonal use of fungal substrate in the cerrado vegetation of Brazil. Insectes Sociaux 47:376-382
• Lutinski J. A., B. C. Lopes, and A. B. B.de Morais. 2013. Diversidade de formigas urbanas (Hymenoptera: Formicidae) de dez cidades do sul do Brasil. Biota Neotrop. 13(3): 332-342.
• Lutinski J. A., F. R. Mello Garcia, C. J. Lutinska, and S. Iop. 2008. Ants diversity in Floresta Nacional de Chapecó in Santa Catarina State, Brazil. Ciência Rural, Santa Maria 38(7): 1810-1816.
• Maravalhas J., and H. L. Vasconcelos. 2014. Revisiting the pyrodiversity–biodiversity hypothesis: long-term fire regimes and the structure of ant communities in a Neotropical savanna hotspot. Journal of Applied Ecology 51: 1661-1668.
• Marinho C. G. S., R. Zanetti, J. H. C. Delabie, M. N. Schlindwein, and L. de S. Ramos. 2002. Ant (Hymenoptera: Formicidae) Diversity in Eucalyptus (Myrtaceae) Plantations and Cerrado Litter in Minas Gerais, Brazil. Neotropical Entomology 31(2): 187-195.
• Mentone T. O., E. A. Diniz, C. B. Munhae, O. C. Bueno, and M. S. C. Morini. 2011. Composition of ant fauna (Hymenoptera: Formicidae) at litter in areas of semi-deciduous forest and Eucalyptus spp., in Southeastern Brazil. Biota Neotrop. 11(2): http://www.biotaneotropica.org.br/v11n2/en/abstract?inventory+bn00511022011.
• Miranda P. N., F. B. Baccaro, E. F. Morato, M. A. Oliveira. J. H. C. Delabie. 2017. Limited effects of low-intensity forest management on ant assemblages in southwestern Amazonian forests. Biodivers. Conserv. DOI 10.1007/s10531-017-1368-y
• Oliveira Mentone T. de, E. A. Diniz, C. de Bortoli Munhae, O. Correa Bueno and M. S. de Castro Morini. 2012. Composition of ant fauna (Hymenoptera: Formicidae) at litter in areas of semi-deciduous forest and Eucalyptus spp., in Southeastern Brazil. Biota Neotrop 11(2): 237-246.
• Pacheco R., and H. L. Vasconcelos. 2012. Subterranean Pitfall Traps: Is ItWorth Including Them in Your Ant Sampling Protocol? Psyche doi:10.1155/2012/870794
• Pires de Prado L., R. M. Feitosa, S. Pinzon Triana, J. A. Munoz Gutierrez, G. X. Rousseau, R. Alves Silva, G. M. Siqueira, C. L. Caldas dos Santos, F. Veras Silva, T. Sanches Ranzani da Silva, A. Casadei-Ferreira, R. Rosa da Silva, and J. Andrade-Silva. 2019. An overview of the ant fauna (Hymenoptera: Formicidae) of the state of Maranhao, Brazil. Pap. Avulsos Zool. 59: e20195938.
• Rabeling C., and M. Bacci. 2010. A new workerless inquiline in the Lower Attini (Hymenoptera: Formicidae), with a discussion of social parasitism in fungus-growing ants. Systematic Entomology 35: 379-392.
• Ramos L. S., R. Z. B. Filho, J. H. C. Delabie, S. Lacau, M. F. S. dos Santos, I. C. do Nascimento, and C. G. S. Marinho. 2003. Ant communities (Hymenoptera: Formicidae) of the leaf-litter in cerrado “stricto sensu” areas in Minas Gerais, Brazil. Lundiana 4(2): 95-102.
• Ramos L. de S., C. G. S. Marinho, R. Zanetti, and J. H. C. Delabie. 2003. Impacto de iscas formicidas granuladas sobre a mirmecofauna não-alvo em eucaliptais segundo duas formas de aplicacação / Impact of formicid granulated baits on non-target ants in eucalyptus plantations according to two forms of application. Neotropical Entomology 32(2): 231-237.
• Ramos L. de S., R. Zanetti, C. G. S. Marinho, J. H. C. Delabie, M. N. Schlindwein, and R. P. Almado. 2004. Impact of mechanical and chemical weedings of Eucalyptus grandis undergrowth on an ant community (Hymenoptera: Formicidae). Rev. Árvore 28(1): 139-146.
• Ribas C. R., J. H. Schoereder, M. Pic, and S. M. Soares. 2003. Tree heterogeneity, resource availability, and larger scale processes regulating arboreal ant species richness. Austral Ecology 28(3): 305-314.
• Rosa da Silva R. 1999. Formigas (Hymenoptera: Formicidae) do oeste de Santa Catarina: historico das coletas e lista atualizada das especies do Estado de Santa Catarina. Biotemas 12(2): 75-100.
• Santschi F. 1925. Nouvelles fourmis brésiliennes. Annales de la Société Entomologique de Belgique. 64: 5-20.
• Santschi F. 1933. Fourmis de la République Argentine en particulier du territoire de Misiones. Anales de la Sociedad Cientifica Argentina. 116: 105-124.
• Schoereder J. H., T. G. Sobrinho, M. S. Madureira, C. R. Ribas, and P. S. Oliveira. 2010. The arboreal ant community visiting extrafloral nectaries in the Neotropical cerrado savanna. Terrestrial Arthropod Reviews 3: 3-27.
• Silvestre R., C. R. F. Brandão, and R. R. Silva da 2003. Grupos funcionales de hormigas: el caso de los gremios del cerrado. Pp. 113-148 in: Fernández, F. (ed.) 2003. Introducción a las hormigas de la región Neotropical. Bogotá: Instituto de Investigación de Recursos Biológicos Alexander von Humboldt, xxvi + 424 pp.
• Silvestre R., M. F. Demetrio, and J. H. C. Delabie. 2012. Community Structure of Leaf-Litter Ants in a Neotropical Dry Forest: A Biogeographic Approach to Explain Betadiversity. Psyche doi:10.1155/2012/306925
• Siqueira de Castro F., A. B. Gontijo, P. de Tarso Amorim Castro, and S. Pontes Ribeiro. 2012. Annual and Seasonal Changes in the Structure of Litter-Dwelling Ant Assemblages (Hymenoptera: Formicidae) in Atlantic Semideciduous Forests. Psyche doi:10.1155/2012/959715
• Siqueira de Castro F., A. B. Gontijo, W. Duarte da Rocha, and S. Pontes Ribeiro. 2011. As comunidades de formigas de serapilheira nas florestas semidecíduas do Parque Estadual do Rio Doce, Minas Gerais. MG.BIOTA, Belo Horizonte 3(5): 5-24.
• Soares S. A., D. Lange, and W. F. Antoniali Junior. 2006. Communities of Epigaeic ants (Hymenoptera: Formicidae) in an area of reforestation and in native forest. Sociobiology 49(3): 251-263.
• Soares S. A., W. F. Antoniali Junior, and S. E. Lima-Junior. 2010. Diversidade de formigas epigéicas (Hymenoptera, Formicidae) em dois ambientes no Centro-Oeste do Brasil. Revista Brasileira de Entomologia 54(1): 76–81.
• Sobrinho T. G., and J. H. Schoereder. 2007. Edge and shape effects on ant (Hymenoptera: Formicidae) species richness and composition in forest fragments. Biodivers Conserv 16: 1459–1470.
• Sobrinho T., J. H. Schoereder, C. F. Sperber, and M. S. Madureira. 2003. Does fragmentation alter species composition in ant communities (Hymenoptera: Formicidae)? Sociobiology 42(2): 329-342.
• Suguituru S. S., M. Santina de Castro Morini, R. M. Feitosa, and R. Rosa da Silva. 2015. Formigas do Alto Tiete. Canal 6 Editora 458 pages
• Theunis, L. , M. Gilbert, Y. Roisin and M. Leponce. 2005. Spatial structure of litter-dwelling ant distribution in a subtropical dry forest. Insectes Sociaux. 52:366–377.
• Vasconcelos H. L., B. B. Araujo, A. J. Mayhé-Nunes. 2008. Patterns of diversity and abundance of fungus-growing ants (Formicidae: Attini) in areas of the Brazilian Cerrado. Revista Brasileira de Zoologia 25(3): 445-450.
• Vittar, F. 2008. Hormigas (Hymenoptera: Formicidae) de la Mesopotamia Argentina. INSUGEO Miscelania 17(2):447-466
• Vittar, F., and F. Cuezzo. "Hormigas (Hymenoptera: Formicidae) de la provincia de Santa Fe, Argentina." Revista de la Sociedad Entomológica Argentina (versión On-line ISSN 1851-7471) 67, no. 1-2 (2008).
• da Silva Araujo, M., Castro Della Lucia, T.M., DA VEIGA, Clayton E y CARDOSO DO NASCIMENTO, Ivan. 2004. Efeito da queima da palhada de cana-de-açúcar sobre comunidade de formicídeos. Ecol. austral. 14(2): 191-200.
• da Silva, R.R., C.R.F. Brandao, and R. Silvestre. 2004. Similarity Between Cerrado Localities in Central and Southeastern Brazil Based on the Dry Season Bait Visitors Ant Fauna. Studies on Neotropical Fauna and Environment 39(3):191-199.