Odontomachus chelifer

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Odontomachus chelifer
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Formicidae
Subfamily: Ponerinae
Tribe: Ponerini
Genus: Odontomachus
Species: O. chelifer
Binomial name
Odontomachus chelifer
(Latreille, 1802)

Odontomachus chelifer casent0173536 profile 1.jpg

Odontomachus chelifer casent0173536 dorsal 1.jpg

Specimen labels


De la Mora et al. (2016) found this species nesting in logs found in coffee farms and forests in the Soconusco region of Chiapas, Mexico. A small percentage of pupae were found to be parasitized by eucharitid wasps.

At a Glance • Polygynous  



Keys including this Species


Distribution based on Regional Taxon Lists

Neotropical Region: Argentina, Bolivia, Brazil, Colombia, Costa Rica, French Guiana, Guatemala, Guyana, Honduras, Mexico, Panama, Paraguay, Peru, Suriname, Venezuela.

Distribution based on AntMaps


Distribution based on AntWeb specimens

Check data from AntWeb


Rosumek (2017) assessed trophic resource use and period of activity within the ant community in a southern Brazil Atlantic forest. For this species: Odontomachus chelifer and Pachycondyla striata are two widespread species that differ radically in morphology but are similar in many aspects. It is appropriate to discuss both together. They are one of the most conspicuous elements of the southern Atlantic forest ground fauna, due to their abundance, solitary foraging mode and large size. Several accounts show these species occupy a multitude of functional roles and have a broad trophic niche. Observation of nest entrances showed that 80-90% of the items carried by P. striata were arthropod parts, mostly termites and other ants, with the remainder consisting of plant material (Giannotti & Machado, 1991; Medeiros & Oliveira, 2009). Through direct observation, Medeiros and Oliveira (2009) also showed that scavenging accounts for more than 80% of its foraging behavior. On the other hand, Fowler (1980) reported O. chelifer prefers certain termite species in the laboratory, and qualitatively stated that in the field prey consisted almost entirely of termites. In the Atlantic forest, all items carried to nests were arthropods, mainly termites, but other animal groups accounted for 60% of them (Raimundo et al., 2009). Scavenging was also cited in this study, although not quantified. Both O. chelifer and P. striata were recorded on experimental carcasses predating the larvae and pupae of necrophagous insects (Paula et al., 2016).

Other important items used by the two species are seeds with elaiosomes and other fallen diaspores rich in proteins and lipids, frequently collected from the ground in the Atlantic forest (Pizo & Oliveira, 2000; Passos & Oliveira, 2002, 2004). Field records on use of liquid sugars are scant and qualitative. Odontomachus chelifer was not observed using extra-floral nectaries by Raimundo et al. (2009), while there is one record for P. striata (in Cerrado, the Brazilian savannah – Byk & Del-Claro, 2010).

The results presented here are mostly consistent with this broader picture. Both species more frequently foraged upon dead insects, sucrose and large prey. In fact, they were the only two species consistently recorded on crickets. The low frequency in termite baits is unexpected and probably represents a methodological artifact. These large solitary foragers were observed quickly collecting termites (even glued ones) and leaving the baits in a few minutes, contrary to ants of smaller species that recruited to them. In cricket baits, however, the two species spent more time trying to carry out the tied cricket or dismembering it. Smaller ants frequently took advantage of this to grab the remains or lick spilled hemolymph. This largely contributed to the richness found in this bait and could happen in nature, whenever predators kill prey too large to carry them out at once.

Besides predation, scavenging was a common behavior, and P. striata in particular would prioritize it whenever possible, in accordance with what was observed by Medeiros and Oliveira (2009). This could be result of their morphology, because the triangular mandibles may be more suited to chop large carcasses than the trap-jaws of O. chelifer. In addition, it could be an effect of competition. The two species were never found at the same bait, and co-occurred in just 10 of the 62 points where they were recorded. The two were previously reported to avoid each other, but, when agonistic interactions occur, P. striata usually is the winner, and can steal the food or kill (and eat) O. chelifer (Medeiros & Oliveira, 2009; Raimundo et al., 2009). Thus, P. striata could displace O. chelifer and maintain control of a valuable resource such as dead arthropods through tandem recruitment (Medeiros & Oliveira, 2009; Silva-Melo & Giannotti, 2012), while cooperative foraging behavior was not observed in O. chelifer (Raimundo et al., 2009). Effectively, the average numbers of workers per bait was smaller for the latter species (O. chelifer = 1.4 ± 0.9; P. striata = 2.5 ± 2; Mann-Whitney, z = -2.27, p = 0.02).

Both species used sucrose frequently and rarely foraged on melezitose (anolog for honeydew). They were never observed foraging on trees or low vegetation in this study, which fits previous accounts (Fowler, 1980; Medeiros & Oliveira 2009), so it is unlikely that they commonly use nectar as food source. This behavior also should limit honeydew use by them.

Past results have shown that these species show a preference for day (P. striata) or night foraging (O. chelifer). No preference in their time of foraging was found in this study.

Lange et al. (2015) - This species was found in semideciduous mesophytic forest pitfall-trap samples. The study examined the ant community within a patch (11.2 hectares) of forest in an urban park (Araguari, Brazil).

Association with Other Organisms

This species is a host for the eucharitid wasp Latina rugosa (a parasite) (Universal Chalcidoidea Database) (associate, primary host).




The following information is derived from Barry Bolton's New General Catalogue, a catalogue of the world's ants.

  • chelifer. Formica chelifera Latreille, 1802c: 188, pl. 8, fig. 51 (w.) SOUTH AMERICA (no locality given). Forel, 1909a: 252 (q.m.); Wheeler, G.C. & Wheeler, J. 1952c: 651 (l.). Combination in Odontomachus: Latreille, 1809: 128. Senior synonym of emacerata: Brown, 1976a: 103; of leptocephalus: Emery, 1911d: 114; of theresiae: Forel, 1899c: 19; Brown, 1976a: 103.
  • leptocephalus. Odontomachus chelifer var. leptocephalus Emery, 1890b: 45, pl. 5, fig. 2 (w.) BRAZIL. Junior synonym of chelifer: Emery, 1911d: 114.
  • theresiae. Odontomachus haematodes r. theresiae Forel, 1895a: 41 (w.) MEXICO. Emery, 1901a: 53 (m.). Subspecies of chelifer: Emery, 1901a: 53; Forel, 1912c: 28; Kempf, 1972a: 170. Junior synonym of chelifer: Forel, 1899c: 19; Brown, 1976a: 103.
  • emacerata. Odontomachus chelifer var. emacerata Santschi, 1922d: 243 (w.) BRAZIL. Junior synonym of chelifer: Brown, 1976a: 103.



  • 2n = 44, karyotype = 4SM+40T (Brazil) (Santos et al., 2010).


  • Brown, W. L., Jr. 1976c. Contributions toward a reclassification of the Formicidae. Part VI. Ponerinae, tribe Ponerini, subtribe Odontomachiti. Section A. Introduction, subtribal characters. Genus Odontomachus. Stud. Entomol. 19: 67-171 (page 103, Senior synonym of emacerata, Senior synonym of theresiae)
  • de la Mora, A., G. Perez-Lachaud, J. P. Lachaud, and S. M. Philpott. 2015. Local and Landscape Drivers of Ant Parasitism in a Coffee Landscape. Environmental Entomology. 44:939-950. doi:10.1093/ee/nvv071
  • Emery, C. 1911e. Hymenoptera. Fam. Formicidae. Subfam. Ponerinae. Genera Insectorum 118: 1-125 (page 114, Senior synonym of leptocephalus)
  • Forel, A. 1899b. Formicidae. [part]. Biol. Cent.-Am. Hym. 3: 1-24 (page 19, Senior synonym of theresiae)
  • Forel, A. 1909a. Ameisen aus Guatemala usw., Paraguay und Argentinien (Hym.). Dtsch. Entomol. Z. 1909: 239-269 (page 252, queen, male described)
  • Lange, D., A. A. Vilela, G. Erdogmus, A. B. Barbosa, S. C. Costa, and V. Stefani. 2015. Temporal dynamic of foraging of epigeic ants in an urban forest fragment. Bioscience Journal. 31:1501-1511.
  • Latreille, P. A. 1802b. Histoire naturelle générale et particulière des Crustacés et des insectes. Tome 3. Familles naturelles des genres. Paris: F. Dufart, xii + 467 pp. (page 188, pl. 8, fig. 51 worker described)
  • Latreille, P. A. 1809. Genera crustaceorum et insectorum secundum ordinem naturalem in familias disposita, iconibus exemplisque plurimus explicata. Tomus 4. Parisiis et Argentorati [= Paris and Strasbourg]: A. Koenig, 399 pp. (page 128, Combination in Odontomachus)
  • Rosumek, F. B. 2017. Natural History of Ants: What We (do not) Know about Trophic and Temporal Niches of Neotropical Species. Sociobiology. 64:244-255. doi:10.13102/sociobiology.v64i3.1623
  • Wheeler, G. C.; Wheeler, J. 1952c. The ant larvae of the subfamily Ponerinae - Part II. Am. Midl. Nat. 48: 604-672 (page 651, larva described)