Cyphomyrmex cornutus

AntWiki: The Ants --- Online
Cyphomyrmex cornutus
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Formicidae
Subfamily: Myrmicinae
Tribe: Attini
Genus: Cyphomyrmex
Species: C. cornutus
Binomial name
Cyphomyrmex cornutus
Kempf, 1968

Cyphomyrmex cornutus casent0052778 profile 1.jpg

Cyphomyrmex cornutus casent0052778 dorsal 1.jpg

Specimen labels

Photo Gallery

  • Cyphomyrmex cornutus grows yeast fungus. Notice that the yeast pebbles are stacked on top of a beetle elytron, which can be found in basically all nests of this species. Photo by Phil Hoenle.

Identification

Mera-Rodriguez, et al. (2020) - Cephalic and mesonotal protuberances horn-like; preocular carina curves above eye; frontal lobes broadly expanded, semicircular; pronotum without median paired denticles, humeral prominence weakly developed and postero-lateral tubercle more developed, antero-ventral corner rectangular; and mesonotum with anterior pair of very prominent spines and posterior pair of very low denticles (Kempf 1968).

Distribution

Mera-Rodriguez, et al. (2020) - Widely distributed across Central and South America: recorded from Veracruz state in Mexico, south to Costa Rica, Colombia, Ecuador, French Guiana, and the Brazilian states of Acre and Bahia. This ample and somewhat disjunct distribution suggests that C. cornutus might have a continuous distribution throughout Central America and northern South America (Adams and Longino 2007; Miranda et al. 2012; Vergara-Navarro and Serna 2013; San- tos et al. 2017).

Latitudinal Distribution Pattern

Latitudinal Range: 18.3212° to -13.342222°.

 
North
Temperate
North
Subtropical
Tropical South
Subtropical
South
Temperate

Distribution based on Regional Taxon Lists

Neotropical Region: Colombia (type locality), Costa Rica, Peru.

Distribution based on AntMaps

AntMapLegend.png

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.
pChart

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.
pChart


Biology

Explore-icon.png 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.

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.

Coral Fungus Agriculture

Practiced by species in the Apterostigma pilosum species-group, which cultivate fungi within the Pterulaceae.

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.

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.

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.

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. ‎

Adams et al. (2015) found that workers of Cyphomyrmex costatus, the host of Megalomyrmex mondaboroides and Megalomyrmex silvestrii, react to a sting by Megalomyrmex parasites mainly with submissive behavior, playing dead or retreating. Host submission also followed brief antennal contact. The observed behavior of Cyphomyrmex costatus was similar to that of Cyphomyrmex cornutus, host of Megalomyrmex mondabora, suggesting that the alkaloidal venoms with pyrrolidines from M. mondabora, piperidines from M. mondaboroides, and pyrolizidines from M. silvestrii may function similarly as appeasement and repellent allomones against host ants, despite their different chemical structure. With the use of these chemical weapons, Megalomyrmex thief ants are met with little host resistance and easily exploit host colony resources.

Association with Other Organisms

Explore-icon.png Explore: Show all Associate data or Search these data. See also a list of all data tables or learn how data is managed.

This species is a host for the ant Megalomyrmex mondabora (a xenobiont) in Costa Rica (Adams et al., 2015).

Castes

Nomenclature

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

  • cornutus. Cyphomyrmex cornutus Kempf, 1968a: 35, figs. 1-4 (w.q.) COLOMBIA.
    • Type-material: holotype worker, 27 paratype workers, 4 paratype queens.
    • Type-locality: holotype Colombia: Valle, 3.2 km. E Rio Aguaclara, on Old Cali Road, 19.iii.1967 (R.B. Root & W.L. Brown); paratypes: 19 workers, 3 queens with same data, 8 workers, 1 queen Colombia: Mun. Buenaventura (Bajo Calima), 16-17.iii.1967 (R.B. Root & W.L. Brown).
    • Type-depositories: MCZC (holotype); DZSP, MCZC, MZSP (paratypes).
    • Status as species: Kempf, 1972a: 92; Snelling, R.R. & Longino, 1992: 485; Bolton, 1995b: 167; Fernández & Serna, 2019: 850.
    • Distribution: Brazil, Colombia, Costa Rica, Ecuador, French Guiana.

Description

Karyotype

Explore-icon.png Explore: Show all Karyotype data or Search these data. See also a list of all data tables or learn how data is managed.
  • 2n = 22, karyotype = 10M+12SM (French Guiana) (Mariano et al., 2011).

References

References based on Global Ant Biodiversity Informatics

  • Adams, R.M.M. and J.T. Longino. 2007. Nesting biology of the arboreal fungus-growing ant Cyphomyrmex cornutus and behavioral interactions with the social-parasitic ant Megalomyrmex mondabora. Insectes Sociaux 54:136-143
  • Bustos H., J. 1994. Contribucion al conocimiento de al fauna de hormigas (Hymenoptera: Formicidae) del occidente del Departamento de Narino (Colombia). Bol. Mus. Ent. Univ. Valle 2(1,2):19-30
  • Dattilo W. et al. 2019. MEXICO ANTS: incidence and abundance along the Nearctic-Neotropical interface. Ecology https://doi.org/10.1002/ecy.2944
  • Fernández F., E. E. Palacio, W. P. Mackay, and E. S. MacKay. 1996. Introducción al estudio de las hormigas (Hymenoptera: Formicidae) de Colombia. Pp. 349-412 in: Andrade M. G., G. Amat García, and F. Fernández. (eds.) 1996. Insectos de Colombia. Estudios escogidos. Bogotá: Academia Colombiana de Ciencias Exactas, Físicas y Naturales, 541 pp
  • Fichaux M., B. Bechade, J. Donald, A. Weyna, J. H. C. Delabie, J. Murienne, C. Baraloto, and J. Orivel. 2019. Habitats shape taxonomic and functional composition of Neotropical ant assemblages. Oecologia 189(2): 501-513.
  • Franco W., N. Ladino, J. H. C. Delabie, A. Dejean, J. Orivel, M. Fichaux, S. Groc, M. Leponce, and R. M. Feitosa. 2019. First checklist of the ants (Hymenoptera: Formicidae) of French Guiana. Zootaxa 4674(5): 509-543.
  • INBio Collection (via Gbif)
  • 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
  • Longino J. T. L., and M. G. Branstetter. 2018. The truncated bell: an enigmatic but pervasive elevational diversity pattern in Middle American ants. Ecography 41: 1-12.
  • Longino J. T., and R. K. Colwell. 2011. Density compensation, species composition, and richness of ants on a neotropical elevational gradient. Ecosphere 2(3): 16pp.
  • Longino J. et al. ADMAC project. Accessed on March 24th 2017 at https://sites.google.com/site/admacsite/
  • Mariano C. S. F., I. da Silva Santos, S. Groc, C. Leroy, P.-J. Malé, M. X. Ruiz-Gonzales, P. Cerdan, A. Dejean, and J. H. C. Delabie. 2011. Th e karyotypes of Gigantiops destructor (Fabricius) and other ants from French Guiana (Formicidae). Ann. soc. entomol. Fr. (n.s.) 47 (1–2): 140-146
  • Sandoval V. E., and G. Zambrano. 2007. Catálogo de las hormigas presentes en el Museo de Historia Natural de la Universidad del Cauca. Taller Editorial de la Universidad del Cauca, Popayán. 60 pp.
  • Snelling R. R., and J. T. Longino. 1992. Revisionary notes on the fungus-growing ants of the genus Cyphomyrmex, rimosus group (Hymenoptera: Formicidae: Attini). Pp. 479-494 in: Quintero, D.; Aiello, A. (eds.) 1992. Insects of Panama and Mesoamerica: selected studies. Oxford: Oxford University Press, xxii + 692 pp.
  • Solomon S. E., C. Rabeling, J. Sosa-Calvo, C. Lopes, A. Rodrigues, H. L. Vasconcelos, M. Bacci, U. G. Mueller, and T. R. Schultz. 2019. The molecular phylogenetics of Trachymyrmex Forel ants and their fungal cultivars provide insights into the origin and coevolutionary history of ‘higher-attine’ ant agriculture. Systematic Entomology 44: 939–956.