Atta
Atta | |
---|---|
Atta cephalotes | |
Scientific classification | |
Kingdom: | Animalia |
Phylum: | Arthropoda |
Class: | Insecta |
Order: | Hymenoptera |
Family: | Formicidae |
Subfamily: | Myrmicinae |
Tribe: | Attini |
Genus: | Atta Fabricius, 1804 |
Type species | |
Formica cephalotes, now Atta cephalotes | |
Diversity | |
20 species (Species Checklist, Species by Country) | |
Synonyms | |
A genus of fungus growing ants. Leafcutter ants obligately cultivate clonally propagated fungus inside their nest as their main source of food. Larval and adult ants eat fungal mycelium from their fungus gardens, as well as clusters (“staphylae”) of modified hyphal tips (“gongylidia”). Nests of some species can be physically very large and consist of millions of workers. (Hölldobler and Wilson 1990, Dijkstra and Boomsma 2006).
At a Glance | • Fungus Grower |
Identification
See images of species within this genus |
Keys including this Genus
Keys to Species in this Genus
Distribution
Distribution and Richness based on AntMaps
Species by Region
Number of species within biogeographic regions, along with the total number of species for each region.
Afrotropical Region | Australasian Region | Indo-Australian Region | Malagasy Region | Nearctic Region | Neotropical Region | Oriental Region | Palaearctic Region | |
---|---|---|---|---|---|---|---|---|
Species | 0 | 0 | 0 | 0 | 2 | 16 | 0 | 0 |
Total Species | 2841 | 1736 | 3045 | 932 | 835 | 4379 | 1741 | 2862 |
Biology
Atta species have a profound influence on the habitats where they live. A review by Swanson et al. (2019) summarized what has been found about their ecological effects on ecosystems: abstract - Leaf-cutter ants are a prominent feature in Neotropical ecosystems, but a comprehensive assessment of their effects on ecosystem functions is lacking. We reviewed the literature and used our own recent findings to identify knowledge gaps and develop a framework to quantify the effects of leaf-cutter ants on ecosystem processes. Leaf-cutter ants disturb the soil structure during nest excavation changing soil aeration and temperature. They mix relatively nutrient-poor soil from deeper layers with the upper organic-rich layers increasing the heterogeneity of carbon and nutrients within nest soils. Leaf-cutter ants account for about 25% of all herbivory in Neotropical forest ecosystems, moving 10%-15% of leaves in their foraging range to their nests. Fungal symbionts transform the fresh, nutrient-rich vegetative material to produce hyphal nodules to feed the ants. Organic material from roots and arbuscular mycorrhizal fungi enhances carbon and nutrient turnover in nest soils and creates biogeochemical hot spots. Breakdown of organic matter, microbial and ant respiration, and nest waste material decomposition result in increased CO2, CH4, and N2O production, but the build-up of gases and heat within the nest is mitigated by the tunnel network ventilation system. Nest ventilation dynamics are challenging to measure without bias, and improved sensor systems would likely solve this problem. Canopy gaps above leaf-cutter ant nests change the light, wind and temperature regimes, which affects ecosystem processes. Nests differ in density and size depending on colony age, forest type and disturbance level and change over time resulting in spatial and temporal changes of ecosystem processes. These characteristics remain a challenge to evaluate rapidly and non-destructively. Addressing the knowledge gaps identified in this synthesis will bring insights into physical and biological processes driving biogeochemical cycles at the nest and ecosystem scale and will improve our understanding of ecosystem biogeochemical heterogeneity and larger scale ecological phenomena.
Dijkstra and Boomsma (2006) investigated the viability of worker-produced eggs in Atta cephalotes, Atta sexdens and Atta colombica. Most Atta workers have rudimentary, non-functional ovaries in a queenright colony but a few, typically tending the queen, can produce trophic eggs (Dijkstra et al., 2005). These eggs are feed to the queen. It was not known if any worker eggs can produce males. This study found, and concluded: Atta workers are not completely infertile, but worker fertility is low compared to the sister genus Acromyrmex, where workers routinely produce normally-size males after queen loss in the laboratory. Most worker eggs did not contain yolk but a small number did and yielded morphologically correct but very small males. They hypothesize that worker reproduction in orphaned Atta field colonies is almost never successful because the last workers die before their sons can be raised to adulthood, but the importance of worker-laid trophic eggs for queen feeding has precluded the evolutionary loss of worker ovaries.
Association with Other Organisms
- Explore: Show all Associate data or Search these data. See also a list of all data tables or learn how data is managed.
Species Uncertain
- An unknown species is a host for the phorid fly Apocephalus vicosae (a parasite) (phorid.net) (attacked).
- An unknown species is a prey for the phorid fly Dohrniphora curvispinosa (a predator) (Quevillon, 2018).
- An unknown species is a associate (details unknown) for the phorid fly Ecitoptera microps (a associate (details unknown)) (Quevillon, 2018).
- An unknown species is a host for the phorid fly Apocephalus vicosae (a parasitoid) (Quevillon, 2018) (encounter mode primary; direct transmission; transmission outside nest).
- An unknown species is a host for the phorid fly Neodohrniphora declinata (a parasitoid) (Quevillon, 2018) (encounter mode primary; direct transmission; transmission outside nest).
- An unknown species is a host for the fungus Aspergillus flavus (a parasitoid) (Quevillon, 2018) (encounter mode primary; direct transmission; transmission within nest).
- An unknown species is a host for the fungus Beauveria bassiana (a parasitoid) (Quevillon, 2018) (encounter mode primary; direct transmission; transmission within nest).
- An unknown species is a associate (details unknown) for the fungus Fusarium graminearum (a associate (details unknown)) (Quevillon, 2018).
- An unknown species is a associate (details unknown) for the fungus Fusarium oxysporum (a associate (details unknown)) (Quevillon, 2018).
- An unknown species is a associate (details unknown) for the fungus Fusarium solani (a associate (details unknown)) (Quevillon, 2018).
- An unknown species is a associate (details unknown) for the fungus Purpureocillium lilacinum (a associate (details unknown)) (Quevillon, 2018).
- An unknown species is a associate (details unknown) for the fungus Trichoderma atroviride (a associate (details unknown)) (Quevillon, 2018).
All Associate Records for Genus
Taxon | Relationship | Associate Type | Associate Taxon | Associate Relationship | Locality | Source | Notes |
---|---|---|---|---|---|---|---|
Atta | associate (details unknown) | fungus | Fusarium graminearum | associate (details unknown) | Quevillon, 2018 | ||
Atta | associate (details unknown) | fungus | Fusarium oxysporum | associate (details unknown) | Quevillon, 2018 | ||
Atta | associate (details unknown) | fungus | Fusarium solani | associate (details unknown) | Quevillon, 2018 | ||
Atta | associate (details unknown) | fungus | Purpureocillium lilacinum | associate (details unknown) | Quevillon, 2018 | ||
Atta | associate (details unknown) | fungus | Trichoderma atroviride | associate (details unknown) | Quevillon, 2018 | ||
Atta | associate (details unknown) | phorid fly | Ecitoptera microps | associate (details unknown) | Quevillon, 2018 | ||
Atta | host | fungus | Aspergillus flavus | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission within nest | |
Atta | host | fungus | Beauveria bassiana | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission within nest | |
Atta | host | phorid fly | Apocephalus vicosae | parasite | phorid.net | attacked | |
Atta | host | phorid fly | Apocephalus vicosae | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta | host | phorid fly | Neodohrniphora declinata | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta | prey | phorid fly | Dohrniphora curvispinosa | predator | Quevillon, 2018 | ||
Atta cephalotes | associate (details unknown) | phorid fly | Synclinusa spp. | associate (details unknown) | Quevillon, 2018 | ||
Atta cephalotes | host | fungus | Ophiocordyceps unilateralis | pathogen | Asia, North and South America | Shrestha et al., 2017 | |
Atta cephalotes | host | milichiid fly | Milichiella argenteocincta | myrmecophile | Argentina, Bahamas, Bolivia, Brazil, Costa Rica, Dominica, Guyana, Panama, Paraguay, Peru, Puerto Rico, Trinidad, Alabama, Florida | Brake, 2009; Milichiidae online | |
Atta cephalotes | host | milichiid fly | Pholeomyia comans | myrmecophile | Moser & Neff, 1971; Milichiidae online | ||
Atta cephalotes | host | milichiid fly | Pholeomyia texensis | myrmecophile | Texas | Waller, 1980; Milichiidae online | |
Atta cephalotes | host | nematode | Panagrolaimus sp. | parasite | Quevillon, 2018 | multiple encounter modes; indirect transmission; transmission outside nest | |
Atta cephalotes | host | nematode | Pristonchus sp. | parasite | Quevillon, 2018 | multiple encounter modes; indirect transmission; transmission outside nest | |
Atta cephalotes | host | phorid fly | Allochaeta wallerae | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta cephalotes | host | phorid fly | Apocephalus asymmetricus | parasite | phorid.net | attacked | |
Atta cephalotes | host | phorid fly | Apocephalus attophilus | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta cephalotes | host | phorid fly | Apocephalus ritualis | parasite | phorid.net | attacked | |
Atta cephalotes | host | phorid fly | Apocephalus sp. | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta cephalotes | host | phorid fly | Apocephalus spinosus | parasite | phorid.net | attacked | |
Atta cephalotes | host | phorid fly | Eibesfeldtphora attae | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta cephalotes | host | phorid fly | Eibesfeldtphora pala | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta cephalotes | host | phorid fly | Eibesfeldtphora prolixa | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta cephalotes | host | phorid fly | Neodohrniphora curvinervis | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta cephalotes | host | phorid fly | Neodohrniphora sp. 1 | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta cephalotes | host | phorid fly | Neodohrniphora sp. 2 | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta colombica | host | fungus | Ophiocordyceps subramanianii | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta colombica | host | phorid fly | Apocephalus attophilus | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta colombica | host | phorid fly | Apocephalus colombicus | parasite | phorid.net | attacked | |
Atta colombica | host | phorid fly | Eibesfeldtphora pala | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta insularis | associate (details unknown) | phorid fly | Puliciphora cubensis | associate (details unknown) | Quevillon, 2018 | ||
Atta laevigata | host | phorid fly | Allochaeta excedens | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta laevigata | host | phorid fly | Apocephalus attophilus | parasite | phorid.net | attacked | |
Atta laevigata | host | phorid fly | Apocephalus vicosae | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta laevigata | host | phorid fly | Eibesfeldtphora | parasite | Souza & Pereira, 2020 | ||
Atta laevigata | host | phorid fly | Eibesfeldtphora tonhascai | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta laevigata | host | phorid fly | Myrmosicarius | parasite | Souza & Pereira, 2020 | ||
Atta laevigata | host | phorid fly | Neodohrniphora declinata | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta laevigata | host | phorid fly | Neodohrniphora erthali | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta laevigata | host | sarcophagid fly | Helicobia sp. | parasite | Brazil | Barganca et al., 2020 | |
Atta mexicana | host | fungus | Beauveria bassiana | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission within nest | |
Atta mexicana | host | phorid fly | Eibesfeldtphora mexicanae | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta mexicana | host | phorid fly | Neodohrniphora sp. | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta mexicana | host | pteromalid wasp | Spalangia attae | parasite | Universal Chalcidoidea Database | associate | |
Atta robusta | host | phorid fly | Eibesfeldtphora breviloba | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta robusta | host | phorid fly | Eibesfeldtphora digitata | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta robusta | host | phorid fly | Myrmosicarius exrobusta | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta sexdens | associate (details unknown) | phorid fly | Apterophora attophila | associate (details unknown) | Quevillon, 2018 | ||
Atta sexdens | associate (details unknown) | phorid fly | Apterophora borgmeieri | associate (details unknown) | Quevillon, 2018 | ||
Atta sexdens | associate (details unknown) | phorid fly | Apterophora bragancai | associate (details unknown) | Quevillon, 2018 | ||
Atta sexdens | associate (details unknown) | phorid fly | Homalophora attae | associate (details unknown) | Quevillon, 2018 | ||
Atta sexdens | host | fungus | Metarhizium anisopliae | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission within nest | |
Atta sexdens | host | phorid fly | Allochaeta excedens | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta sexdens | host | phorid fly | Apocephalus attophilus | parasite | Farder-Gomes et al., 2020 | ||
Atta sexdens | host | phorid fly | Apocephalus vicosae | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta sexdens | host | phorid fly | Eibesfeldtphora tonhascai | parasite | Farder-Gomes et al., 2020; Souza & Pereira, 2020 | Souza & Pereira, 2020 - genus-level identification only | |
Atta sexdens | host | phorid fly | Eibesfeldtphora trifurcata | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta sexdens | host | phorid fly | Myrmosicarius | parasite | Souza & Pereira, 2020 | very rare | |
Atta sexdens | host | phorid fly | Myrmosicarius crudelis | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta sexdens | host | phorid fly | Myrmosicarius grandicornis | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta sexdens | host | phorid fly | Neodohrniphora acromyrmecis | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta sexdens | host | phorid fly | Neodohrniphora curvinervis | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta sexdens | host | phorid fly | Neodohrniphora declinata | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta sexdens | host | phorid fly | Neodohrniphora elongata | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta sexdens | host | phorid fly | Neodohrniphora sp. | parasite | Braganca et al., 1998 | ||
Atta sexdens | host | phorid fly | Neodohrniphora tonhascai | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta sexdens | prey | phorid fly | Dohrniphora fuscicoxa | predator | Quevillon, 2018 | ||
Atta sexdens | prey | phorid fly | Dohrniphora paraguayana | predator | Quevillon, 2018 | ||
Atta texana | host | diapriid wasp | Coptera pholeomyiae | parasite | www.diapriid.org | potential host | |
Atta texana | host | fungus | Aspergillus flavus | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission within nest | |
Atta texana | host | fungus | Beauveria bassiana | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission within nest | |
Atta texana | host | milichiid fly | Pholeomyia comans | myrmecophile | Moser & Neff, 1971; Muesebeck, 1980 | associated with or potential host | |
Atta texana | host | milichiid fly | Pholeomyia texensis | myrmecophile | Texas | Waller, 1980 | associated with or potential host |
Atta texana | host | phorid fly | Apocephalus wallerae | parasite | phorid.net | attacked | |
Atta texana | host | phorid fly | Megaselia sp. | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta texana | host | phorid fly | Myrmosicarius texanus | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta texana | host | pteromalid wasp | Spalangia attae | parasite | Universal Chalcidoidea Database | associate | |
Atta vollenweideri | host | phorid fly | Apocephalus setitarsus | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta vollenweideri | host | phorid fly | Apocephalus vicosae | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta vollenweideri | host | phorid fly | Eibesfeldtphora trilobata | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta vollenweideri | host | phorid fly | Myrmosicarius brandaoi | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Atta vollenweideri | host | phorid fly | Myrmosicarius gonzalezae | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest |
Flight Period
All Flight Records for Genus
- Explore: Show all Flight Month data or Search these data. See also a list of all data tables or learn how data is managed.
Taxon | Month | Source | Notes |
---|---|---|---|
Atta mexicana | Jun • Jul | antkeeping.info | |
Atta texana | Apr • May • Jun | antkeeping.info |
Life History Traits
- Mean colony size: 1750000 (Greer et al., 2021)
- Compound colony type: not parasitic (Greer et al., 2021)
- Nest site: hypogaeic (Greer et al., 2021)
- Diet class: herbivore (Greer et al., 2021)
- Foraging stratum: subterranean/leaf litter; arboreal (Greer et al., 2021)
- Foraging behaviour: cooperative (Greer et al., 2021)
Castes
Morphology
Worker Morphology
- Explore: Show all Worker Morphology data or Search these data. See also a list of all data tables or learn how data is managed.
• Antennal segment count: 11 • Antennal club: gradual • Palp formula: 4,2 • Total dental count: 8-12 • Spur formula: 0,0 • Eyes: >100 ommatidia • Scrobes: absent • Pronotal Spines: present • Mesonotal Spines: dentiform; present • Propodeal Spines: present • Petiolar Spines: absent • Caste: polymorphic • Sting: absent • Metaplural Gland: present • Cocoon: absent
Karyotype
All Karyotype Records for Genus
- 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.
Taxon | Haploid | Diploid | Karyotype | Locality | Source | Notes |
---|---|---|---|---|---|---|
Atta colombica | 11 | 22 | 12M+6SM+4A | Panama | Murakami et al., 1998; Barros et al., 2014 | ''Atta columbica'' is a writing mistake |
Atta laevigata | 22 | 12M+6SM+4A | Brazil | Fadini & Pompolo, 1996; Barros et al., 2014 | ||
Atta robusta | 22 | 18M+2SM+2ST | Brazil | Barros et al., 2015; de Castro et al., 2020 | ||
Atta sexdens | 22 | 12M+6SM+4A | Brazil | Fadini & Pompolo, 1996; SantosColares et al., 1997; Barros et al., 2014 | ||
Atta sexdens | 22 | 18M + 4A | Brazil | de Castro et al., 2020 | ||
Atta sexdens | 22 | 18M+2SM+2ST | Brazil, French Guiana | Aguiar et al., 2020 |
Phylogeny
Myrmicinae |
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See Phylogeny of Myrmicinae for details.
Nomenclature
The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.
- abdominalis. Oecodoma abdominalis Smith, F. 1858b: 184, pl. 10, fig. 22 (q.) “South America”.
- Type-material: syntype queens (number not stated).
References
- Ashmead, W. H. 1905c. A skeleton of a new arrangement of the families, subfamilies, tribes and genera of the ants, or the superfamily Formicoidea. Can. Entomol. 37: 381-384 (page 384, Atta in Cryptoceridae)
- Baigorria, J.A., Rubio, G.D., Stolar, C.E., Oklander, L.I. 2021. Notes on the jumping spider Corythalia conferta (Araneae: Salticidae), a possible myrmecophagous specialist in Argentina. Peckhamia 230.1, 1-12.
- Barden, P. 2017. Fossil ants (Hymenoptera: Formicidae): ancient diversity and the rise of modern lineages. Myrmecological News 24: 1-30.
- Barrera, C.A., Sosa-Calvo, J., Schultz, T.R., Rabeling, C., Bacci, M., Jr 2021. Phylogenomic reconstruction reveals new insights into the evolution and biogeography of Atta leaf-cutting ants (Hymenoptera: Formicidae). Systematic Entomology 47: 13-35 (doi:10.1111/syen.12513).
- Bolton, B. 2003. Synopsis and Classification of Formicidae. Mem. Am. Entomol. Inst. 71: 370pp (page 197, Atta in Myrmicinae, Attini)
- Borgmeier, T. 1959b. Revision der Gattung Atta Fabricius (Hymenoptera, Formicidae). Stud. Entomol. (n.s.) 2: 321-390 (page 321, Revision of genus)
- Boudinot, B.E. 2019. Hormigas de Colombia. Cap. 15. Clave para las subfamilias y generos basada en machos. Pp. 487-499 in: Fernández, F., Guerrero, R.J., Delsinne, T. (eds.) 2019d. Hormigas de Colombia. Bogotá: Universidad Nacional de Colombia, 1198 pp.
- Branstetter, M.G., Longino, J.T., Reyes- López, J.L., Brady, S.G., Schultz, T.R. 2022. Out of the temperate zone: A phylogenomic test of the biogeographical conservatism hypothesis in a contrarian clade of ants. Journal of Biogeography 00, 1-14 (doi:10.1111/jbi.14462).
- Brown, W. L., Jr. 1973b. A comparison of the Hylean and Congo-West African rain forest ant faunas. Pp. 161-185 in: Meggers, B. J., Ayensu, E. S., Duckworth, W. D. (eds.) Tropical forest ecosystems in Africa and South America: a comparative review. Wash (page 182, Myrmegis (nomen nudum) referable to Atta)
- Burchill, A.T., Moreau, C.S. 2016. Colony size evolution in ants: macroevolutionary trends. Insectes Sociaux 63, 291–298 (doi:10.1007/s00040-016-0465-3).
- Burger, H.F., Vondráčková, K., Skłodowski, M., Qian-Qun Koid, Dent, D.H., Wallace, K., Fayle, T.M. 2021. Protection from herbivores varies among ant genera for the myrmecophilic plant Leea aculeata in Malaysian Borneo. Asian Myrmecology 14, e014002 (doi:10.20362/am.014002).
- Cantone S. 2017. Winged Ants, The Male, Dichotomous key to genera of winged male ants in the World, Behavioral ecology of mating flight (self-published).
- Cantone S. 2018. Winged Ants, The queen. Dichotomous key to genera of winged female ants in the World. The Wings of Ants: morphological and systematic relationships (self-published).
- Cantone, S., Von Zuben, C.J. 2019. The hindwings of ants: A phylogenetic analysis. Psyche: A Journal of Entomology 2019, 1–11 (doi:10.1155/2019/7929717).
- Cherrett, J. M.; Cherrett, F. J. 1989. A bibliography of the leaf-cutting ants, Atta spp. and Acromyrmex spp., up to 1975. Overseas Dev. Nat. Resour. Inst. Bull. 14: 1-58 (page 1, Bibliography)
- Cresson, E. T. 1887. Synopsis of the families and genera of the Hymenoptera of America, north of Mexico, together with a catalogue of the described species, and bibliography. Trans. Am. Entomol. Soc., Suppl. Vol. 1887: 1-351 (page 259, Atta in Myrmicinae [Myrmicidae])
- Cristiano, M.P., Cardoso, D.C., Sandoval‐Gómez, V.E., Simões‐Gomes, F.C. 2020. Amoimyrmex Cristiano, Cardoso, Sandoval, gen. nov. (Hymenoptera: Formicidae): a new genus of leaf‐cutting ants revealed by multilocus molecular phylogenetic and morphological analyses. Austral Entomology 59, 643–676 (doi:10.1111/aen.12493).
- Dalla Torre, K. W. von. 1893. Catalogus Hymenopterorum hucusque descriptorum systematicus et synonymicus. Vol. 7. Formicidae (Heterogyna). Leipzig: W. Engelmann, 289 pp. (page 150, Atta in Myrmicinae)
- Dijkstra, M. B. and J. J. Boomsma. 2006. Are workers of Atta leafcutter ants capable of reproduction? Insectes Sociaux. 53(2):136-140. doi:10.1007/s00040-005-0848-3
- Dijkstra, M. B., D. R. Nash, and J. J. Boomsma. 2005. Self-restraint and sterility in workers of Acromyrmex and Atta leafcutter ants. Insectes Sociaux. 52(1):67-76. doi:10.1007/s00040-004-0775-8
- Emery, C. 1877b. Saggio di un ordinamento naturale dei Mirmicidei, e considerazioni sulla filogenesi delle formiche. Bull. Soc. Entomol. Ital. 9: 67-83 (page 81, Atta in Myrmicinae, Attini [Myrmicidae, Attidae])
- Emery, C. 1895l. Die Gattung Dorylus Fab. und die systematische Eintheilung der Formiciden. Zool. Jahrb. Abt. Syst. Geogr. Biol. Tiere 8: 685-778 (page 770, Atta in Myrmicinae)
- Emery, C. 1914e. Intorno alla classificazione dei Myrmicinae. Rend. Sess. R. Accad. Sci. Ist. Bologna Cl. Sci. Fis. (n.s.) 18: 29-42 (page 42, Atta in Myrmicinae, Attini)
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- Fernandez, F., Guerrero, R.J., Sánchez-Restrepo, A.F. 2021. Sistemática y diversidad de las hormigas neotropicales. Revista Colombiana de Entomología 47, 1–20 (doi:10.25100/socolen.v47i1.11082).
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- Forel, A. 1899d. Formicidae. [part]. Biol. Cent.-Am. Hym. 3: 25-56 (page 30, Atta in Myrmicinae, Attini)
- Forel, A. 1917. Cadre synoptique actuel de la faune universelle des fourmis. Bull. Soc. Vaudoise Sci. Nat. 51: 229-253 (page 247, Atta in Myrmicinae, Attini)
- Hanisch, P.E., Sosa-Calvo, J., Schultz, T.R. 2022. The last piece of the puzzle? Phylogenetic position and natural history of the monotypic fungus-farming ant genus Paramycetophylax (Formicidae: Attini). Insect Systematics and Diversity 6 (1): 11:1-17 (doi:10.1093/isd/ixab029).
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