(Smith, F., 1858)
These aggressive ants prey on termites. When they find a termite nest they can create a foraging trail with a column of ants that contains more than 1,000 workers.
|At a Glance||• Termite specialist|
- 1 Identification
- 2 Distribution
- 3 Biology
- 4 Castes
- 5 Nomenclature
- 6 References
- 7 References based on Global Ant Biodiversity Informatics
Mackay and Mackay (2010): Neoponera laevigata workers and females could be confused with those of three other shiny species: Neoponera commutata, Neoponera marginata and Neoponera carbonaria. Neoponera laevigata can be easily separated from N. commutata and the moderately shiny N. carbonaria by the coarse striae on the side of the propodeum, which are very fine on both of the latter species. The mandibles of N. laevigata are smooth and shining, not dull and striate as in N. commutata and without the longitudinal fold as in N. marginata. The shape of the petiole is very different in N. carbonaria with the anterior face being nearly vertical and the posterior face being convex and meeting the anterior face at an angle and thus not forming a distinct dorsal face. Neoponera laevigata can be separated from N. marginata as the mandible lacks the carina or fold, which separates the inner part of the mandible from the outer part in N. marginata. The mostly shining black surfaces would separate this species from all of the other North American Neoponera.
Southern Central America through central South America, Trinidad. (Mackay and Mackay 2010)
Latitudinal Distribution Pattern
Latitudinal Range: 68.702° to -64.23°.
- Source: AntMaps
Distribution based on Regional Taxon Lists
Distribution based on AntMaps
Distribution based on AntWeb specimens
Check data from AntWeb
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.
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.
Specimens have been collected between 350 and 700 meters in wet forest. (Mackay and Mackay 2010)
Mackay and Mackay (2010): This species nests in the soil under logs or under heavy leaf litter and sometimes occurs within the log. A male was collected in a nest in September (Panamá). A loose male was collected in March (Costa Rica) and winged females in March and October (Brasil) and December (Costa Rica).
Wheeler (1936) provided details on the biology of this species. He reports that C. Haskins found a column moving to a new nest site on Barro Colorado Island. The column was about 1.5 m in length and about 10 cm wide, containing males and females (August). Emerson found raids three times on Barro Colorado Island at midday during July and September (Wheeler, 1936). The columns were about 6 meters long and a single worker wide. The organized columns contain between 500 - 1700 workers (Downing, 1978). The ants were carrying workers and soldiers of the termites Amitermes beaumonti Banks and Heterotermes tenuis (Hagen), both common in dead wood on the forest floor (Wheeler, 1936). Neoponera laevigata is an important predator on the termites Nasutitermes costalis (Traniello, 1981); and prey on termites in the genera Neocapritermes, Microtermes and Coptotermes (Hölldobler and Traniello, 1980) and Speculitermes sp. (Borgmeier, 1959), in addition to the genera mentioned above. Workers are very aggressive and are able to sting.
Workers use a recruitment trail pheromone, which originates from the pygidial gland (Hölldobler and Traniello, 1980) and not, as previously assumed, from the hindgut (Blum, 1966). Baroni Urbani (1993) discussed the evolution of recruitment behavior in N. laevigata.
Association with Other Organisms
- This species is a associate (details unknown) for the phorid fly Ecitomyia juxtaposita (a associate (details unknown)) (Quevillon, 2018).
The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.
- laevigata. Ponera laevigata Smith, F. 1858b: 98 (w.) BRAZIL (Amazonas).
- Type-material: 2 syntype workers.
- Type-locality: Brazil: Ega (= Tefé), “58/6” (H.W. Bates).
- Type-depository: BMNH.
- [Misspelled as levigata by Dalla Torre, 1893: 34.]
- Wheeler, W.M. 1936d: 162 (q.m.).
- Combination in Euponera (Mesoponera): Emery, 1901a: 47;
- combination in Termitopone: Wheeler, W.M. 1936d: 159;
- combination in Pachycondyla: Mayr, 1886c: 358; Brown, in Bolton, 1995b: 306;
- combination in Neoponera: Schmidt, C.A. & Shattuck, 2014: 151.
- Status as species: Mayr, 1863: 448; Mayr, 1886c: 358; Emery, 1892b: 167; Dalla Torre, 1893: 34; Forel, 1895b: 114; Forel, 1899c: 13; Emery, 1911d: 82; Wheeler, W.M. 1916c: 2; Borgmeier, 1923: 71; Wheeler, W.M. 1936d: 161 (redescription); Borgmeier, 1959a: 314; Kempf, 1972a: 249; Bolton, 1995b: 306; Mackay, Mackay, et al. 2008: 195; Mackay & Mackay, 2010: 414 (redescription); Feitosa, 2015c: 99; Fernández & Guerrero, 2019: 534.
- Senior synonym of gagatina: Emery, 1892b: 167; Dalla Torre, 1893: 34; Forel, 1895b: 114; Forel, 1899c: 13; Emery, 1911d: 82; Borgmeier, 1923: 71; Kempf, 1972a: 249; Bolton, 1995b: 306; Mackay & Mackay, 2010: 414.
- Senior synonym of whelpleyi: Wheeler, W.M. 1936d: 164 (in text); Kempf, 1972a: 249; Bolton, 1995b: 306; Mackay & Mackay, 2010: 414.
- Distribution: Brazil, Colombia, Costa Rica, Ecuador, Panama, Trinidad.
- gagatina. Pachycondyla gagatina Emery, 1890a: 75 (w.) COSTA RICA.
- Type-material: syntype workers (number not stated).
- Type-locality: Costa Rica: Jiménez (A. Alfaro).
- Type-depository: MSNG.
- [Also described as new by Emery, 1894k: 48.]
- Status as species: Emery, 1890b: 42.
- Junior synonym of laevigata: Emery, 1892b: 167; Dalla Torre, 1893: 34; Forel, 1895b: 114; Forel, 1899c: 13; Emery, 1911d: 82; Borgmeier, 1923: 71; Kempf, 1972a: 249; Bolton, 1995b: 305; Mackay & Mackay, 2010: 414.
- whelpleyi. Euponera (Mesoponera) laevigata var. whelpleyi Wheeler, W.M. 1922c: 3 (w.) TRINIDAD.
- Type-material: holotype worker.
- Type-locality: Trinidad: Caparo (P.B. Whelpley).
- Type-depository: MCZC.
- Junior synonym of laevigata: Wheeler, W.M. 1936d: 164 (in text); Kempf, 1972a: 249; Bolton, 1995b: 311; Mackay & Mackay, 2010: 414.
Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
Mackay and Mackay (2010): The worker is usually a moderately sized (total length 5 - 10 mm) shiny black ant with dark brown appendages. The eye is relatively large (0.5 mm maximum diameter) with a diameter about twice as long as the distance between the anterior border of the eye and the anterior border of the head (side view). There is no malar carina. The scape extends slightly past the posterior lateral corner of the head. The pronotal shoulder is swollen, but does not form a carina. The dorsum of the mesosoma is nearly straight, the metanotal suture is poorly developed, but present on the dorsum of the mesosoma. The propodeal spiracle is slit-shaped and the posterior face of the propodeum is separated from the sides of the propodeum by a sharp edge. The petiole is thick when viewed in profile, with the anterior face being slightly concave, the posterior face being convex and the dorsal face being well defined. The dorsal face of the petiole is much broader posteriorly than anteriorly (seen from above). The posterior lateral edges of the petiole are sharp between the sides of the petiole and the posterior face. The anterior face of the postpetiole is slightly concave and meets the dorsal face at an angle.
Erect hairs are abundant on most surfaces, including the sides of the head, the shaft of the scape, the dorsal and ventral surfaces of the head, the dorsum of the mesosoma, the legs (most of the hairs on the tibiae and many on the remainder of the legs are suberect), the dorsum of the petiole and all surfaces of the gaster.
Most of the head is smooth and glossy, but distinct poorly defined striae are present on the dorsum, the mesosoma is mostly smooth and glossy, but the upper half of the mesopleuron and the side of the propodeum have well-developed coarse striae. The dorsal face of the propodeum has a few short (0.3 mm in length) poorly developed striae, the posterior face of the propodeum is smooth and glossy. Most of the petiole and gaster are smooth and glossy.
The workers of this species are polymorphic. They may be as small as 5 mm total length, with all sizes up to the length of the largest worker (total length 10 mm). The smaller workers are less sculptured and the entire head may be smooth and glossy.
Mackay and Mackay (2010): The female is a large (total length 13 mm) mostly shiny black ant. The mandible has approximately 11 teeth (basalmost teeth are small and poorly defined) that alternate in size. The anterior margin of the clypeus is broadly convex. The eye is moderately sized (maximum diameter 0.6 mm) located about ⅔ diameter from the anterior margin of the head. The scapes barely reach the posterior lateral corner of the head. The pronotal shoulder is swollen but does not form a well-developed carina. The propodeal spiracle is slit-shaped. The petiole is shaped like that of the worker, moderately thickened when viewed in profile with a slightly concave anterior face and a slightly convex posterior face, which converge dorsally and form a moderately well-developed dorsal face. The subpetiolar process is a lobe, which is angulate ventrally. Erect hairs (up to 0.4 mm in length) are present on the mandibles, clypeus, dorsal and ventral surfaces of the head, sides of the head, posterior margin, scapes, mesosoma, petiole and all surfaces of the gaster, the hairs on the legs are suberect to erect only; appressed pubescence is sparse and only noticeable on the gaster.
The dorsum of the head has longitudinal striae, which diverge posteriorly, the dorsum of the mesosoma is mostly smooth and glossy, as are the side of the pronotum and the anepisternum, the katepisternum and side of the propodeum are striate. The side of the petiole has a little evidence of horizontal striae and is mostly smooth and glossy as is the posterior face. The gaster is nearly completely smooth and glossy.
Mackay and Mackay (2010): The male is a moderately sized (total length 11 mm) shiny black specimen. The mandibles are tiny and have the oval-shaped depression near the base. The anterior margin of the clypeus is convex with the middle of the clypeus being swollen. The eyes are large (maximum diameter 0.74 mm) occupying more than ½ of the side of the head. The ocelli are relatively small (maximum diameter of the medial ocellus is 0.14 mm). The pronotal shoulder is slightly swollen, the propodeal spiracle is elongated. The shape of the petiole is similar to that of the worker, with the anterior face being nearly straight and the posterior face being convex and converging dorsally, forming a broadly rounded dorsal face. The subpetiolar process is similar to that of the female and only slightly less developed.
Erect hairs (up to 0.3 mm in length) are present on the mandibles, clypeus, all surfaces of the head, dorsum of the mesosoma, dorsum of the petiole and all surfaces of the gaster, most hairs on the legs are nearly erect.
Most surfaces are smooth and glossy as in the worker and female.
The name of this species is from the Latin word laevigatus, meaning smooth, referring to the sculpturing of this species. (Mackay and Mackay 2010)
- Mackay, W. P., and E. E. Mackay 2010. The Systematics and Biology of the New World Ants of the Genus Pachycondyla (Hymenoptera: Formicidae). Edwin Mellon Press, Lewiston. Information from this publication is used with permission from the authors.
- 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).
- Araujo, E.S., Koch, E.B.A., Delabie, J.H.C., Zeppelini, D., DaRocha, W.D., Castaño-Meneses, G., Mariano, C.S.F. 2019. Diversity of commensals within nests of ants of the genus Neoponera (Hymenoptera: Formicidae: Ponerinae) in Bahia, Brazil. Annales de la Société entomologique de France (N.S.) 55, 291–299 (doi:10.1080/00379271.2019.1629837).
- Baroni Urbani, C. 1993. The diversity and evolution of recruitment behaviour in ants, with a discussion of the usefulness of parsimony criteria in the reconstruction of evolutionary histories. Insectes Sociaux 40:233-260.
- Blum, M. 1966. The source and specificity of trail pheromones in Termitopone, Monomorium and Huberia and their relation to those of some other ants. Proceedings of the Royal Entomological Society, London 41:155-160.
- Borgmeier, T. 1959. Myrmecologische studien. II. Anais de Academia brasiliera de Ciências 31:309-319.
- Brown, W. L., Jr. 1995a. [Untitled. Taxonomic changes in Pachycondyla attributed to Brown.] Pp. 302-311 in: Bolton, B. A new general catalogue of the ants of the world. Cambridge, Mass.: Harvard University Press, 504 pp. (page 306, Combination in Pachycondyla)
- Downing, H. 1978. Foraging and migratory behavior of the ponerine ant Termitopone laevigata. Bachelor’s of Arts thesis, Smith College, Northampton, MA.
- Emery, C. 1892c . Note sinonimiche sulle formiche. Bull. Soc. Entomol. Ital. 23: 159-167 (page 167, Senior synonym of gagatina)
- Emery, C. 1901b. Notes sur les sous-familles des Dorylines et Ponérines (Famille des Formicides). Ann. Soc. Entomol. Belg. 45: 32-54 (page 47, Combination in Euponera (Mesoponera))
- Esteves, F.A., Fisher, B.L. 2021. Corrieopone nouragues gen. nov., sp. nov., a new Ponerinae from French Guiana (Hymenoptera, Formicidae). ZooKeys 1074, 83–173 (doi:10.3897/zookeys.1074.75551).
- Franco, W., Ladino, N., Delabie, J.H.C., Dejean, A., Orivel, J., Fichaux, M., Groc, S., Leponce, M., Feitosa, R.M. 2019. First checklist of the ants (Hymenoptera: Formicidae) of French Guiana. Zootaxa 4674, 509–543 (doi:10.11646/zootaxa.4674.5.2).
- Hölldobler, B. and Traniello, J. F. 1980. The pygidial gland and chemical recruitment in Pachycondyla (= Termitopone) laevigata. Journal of Chemical Ecology 6:883-893.
- Mayr, G. 1886c. Notizen über die Formiciden-Sammlung des British Museum in London. Verh. K-K. Zool.-Bot. Ges. Wien 36: 353-368 (page 358, Combination in Pachycondyla)
- Schmidt, C.A. & Shattuck, S.O. 2014. The higher classification of the ant subfamily Ponerinae (Hymenoptera: Formicidae), with a review of ponerine ecology and behavior. Zootaxa 3817, 1–242 (doi:10.11646/zootaxa.3817.1.1).
- Smith, F. 1858a. Catalogue of hymenopterous insects in the collection of the British Museum. Part VI. Formicidae. London: British Museum, 216 pp. (page 98, worker described)
- Traniello, J. F. 1981. Enemy deterrence in the recruitment strategy of a termite: soldier-organized foraging in Nasutitermes costalis. Proceedings of the National Academy of Science 78:1976-1979.
- Wheeler, W. 1936. Ecological relations of ponerine and other ants to termites. Proceedings of the American Academy of Arts and Sciences 71:159-243.
References based on Global Ant Biodiversity Informatics
- Alonso L. E., J. Persaud, and A. Williams. 2016. Biodiversity assessment survey of the south Rupununi Savannah, Guyana. BAT Survey Report No.1, 306 pages.
- Andrade T., G. D. V. Marques, K. Del-Claro. 2007. Diversity of ground dwelling ants in Cerrado: an analysis of temporal variations and distinctive physiognomies of vegetation (Hymenoptera: Formicidae). Sociobiology 50(1): 121-134.
- Borgmeier T. 1959. Myrmecologische Studien. II. Anais da Academia Brasileira de Ciencias 31: 309-319.
- Carvalho Pereira L. P. 2012. Estrutura da comunidade de formigas poneromorfas (Hymenoptera:Formicidae) em uma área da Floresta Amazônica. Master Thesis Universidade Federal Rural do Rio de Janeiro. 64 pages.
- 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.
- Fernández F., and T. M. Arias-Penna. 2008. Las hormigas cazadoras en la región Neotropical. Pp. 3-39 in: Jiménez, E.; Fernández, F.; Arias, T.M.; Lozano-Zambrano, F. H. (eds.) 2008. Sistemática, biogeografía y conservación de las hormigas cazadoras de Colombia. Bogotá: Instituto de Investigación de Recursos Biológicos Alexander von Humboldt, xiv + 609 pp.
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- Groc S., J. H. C. Delabie, F. Fernandez, M. Leponce, J. Orivel, R. Silvestre, Heraldo L. Vasconcelos, and A. Dejean. 2013. Leaf-litter ant communities (Hymenoptera: Formicidae) in a pristine Guianese rainforest: stable functional structure versus high species turnover. Myrmecological News 19: 43-51.
- INBio Collection (via Gbif)
- Kempf, W.W. 1972. Catalago abreviado das formigas da regiao Neotropical (Hym. Formicidae) Studia Entomologica 15(1-4).
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- Wheeler W. M. 1922. The ants of Trinidad. American Museum Novitates 45: 1-16.
- Wheeler W. M. 1936. Ecological relations of ponerine and other ants to termites. Proceedings of the American Academy of Arts and Sciences. 71: 159-243.