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Strumigenys metopia

AntWiki: The Ants --- Online
Strumigenys metopia
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Formicidae
Subfamily: Myrmicinae
Tribe: Attini
Genus: Strumigenys
Species: S. metopia
Binomial name
Strumigenys metopia
(Brown, 1959)

Specimen Labels

The two records of this species are from rainforest and a bamboo forest. Both were obtained via litter sampling.

Identification

Bolton (2000) - A member of the crassicornis-complex in the Strumigenys gundlachi group. The minute metopia is the only known species of the crassicornis-complex to possess flagellate hairs on the alitrunk.

Keys including this Species

Distribution

Latitudinal Distribution Pattern

Latitudinal Range: 4.096388889° to -2.517°.

 
North
Temperate 		North
Subtropical 		Tropical South
Subtropical 		South
Temperate

Distribution based on Regional Taxon Lists

Neotropical Region: Brazil, Colombia, Ecuador, French Guiana, Panama (type locality), Peru.

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.
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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.
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Biology

Explore Overview of Strumigenys biology 
Strumigenys were once thought to be rare. The development and increased use of litter sampling methods has led to the discovery of a tremendous diversity of species. Many species are specialized predators (e.g. see Strumigenys membranifera and Strumigenys louisianae). Collembola (springtails) and other tiny soil arthropods are typically favored prey. Species with long linear mandibles employ trap-jaws to sieze their stalked prey (see Dacetine trap-jaws). Larvae feed directly on insect prey brought to them by workers. Trophallaxis is rarely practiced. Most species live in the soil, leaf litter, decaying wood or opportunistically move into inhabitable cavities on or under the soil. Colonies are small, typically less than 100 individuals but in some species many hundreds. Moist warm habitats and micro-habitats are preferred. A few better known tramp and otherwise widely ranging species tolerate drier conditions. Foraging is often in the leaf litter and humus. Workers of many species rarely venture above ground or into exposed, open areas. Individuals are typically small, slow moving and cryptic in coloration. When disturbed individuals freeze and remain motionless. Males are not known for a large majority of species.

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Castes

Nomenclature

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

  • metopia. Neostruma metopia Brown, 1959b: 11, fig. 2 (q.) PANAMA. Kempf, 1975a: 417 (w.). Combination in Pyramica: Bolton, 1999: 1672; in Strumigenys: Baroni Urbani & De Andrade, 2007: 124. See also: Bolton, 2000: 190.

Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.

Description

Worker

Bolton (2000) - TL 1.5-1.6, HL 0.40-0.41, HW 0.29-0.31, CI 72-75, ML 0.12-0.13, MI 30-31, SL 0.17-0.19, SI 60-63, PW 0.20-0.22, AL 0.38-0.40 (4 measured). Characters of crassicornis complex. Submedian tooth of mandible strongly developed; 3 minute denticles distal of submedian tooth and 2 proximal of it. Scape expanded at subbasal angle (similar to development seen in Strumigenys crassicornis but not as extensive), the scape distinctly broadest at this point, tapering to apex. Apicoscrobal hair curved and elongate. Pair of standing hairs on cephalic dorsum close to occipital margin may be only weakly differentiated from the conspicuous spatulate ground-pilosity. Pronotal humeral hair long and flagellate. Mesonotum with a single pair of long flagellate hairs. Postpetiole in profile swollen, subglobular; spongiform lobes very reduced.

Type Material

Holotype queen (dealate), PANAMA: Barro Colorado Island, 1938, no. 871 (N.A. Weber) (examined).

References

References based on Global Ant Biodiversity Informatics

  • Bolton, B. 2000. The Ant Tribe Dacetini. Memoirs of the American Entomological Institute 65
  • Brandao, C.R.F. 1991. Adendos ao catalogo abreviado das formigas da regiao neotropical (Hymenoptera: Formicidae). Rev. Bras. Entomol. 35: 319-412.
  • Brown W. L. Jr. 1959. A revision of the dacetine ant genus Neostruma. Breviora 107: 1-13.
  • 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
  • Fernández, F. and S. Sendoya. 2004. Lista de las hormigas neotropicales. Biota Colombiana Volume 5, Number 1.
  • 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.
  • 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.
  • Groc S., J. Orivel, A. Dejean, J. Martin, M. Etienne, B. Corbara, and J. H. C. Delabie. 2009. Baseline study of the leaf-litter ant fauna in a French Guianese forest. Insect Conservation and Diversity 2: 183-193.
  • Kempf W. W. 1975. Report on Neotropical Dacetine ant studies (Hymenoptera: Formicidae). Revista Brasileira de Biologia 34: 411-424.
  • Mertl A. L., J. F. A. Traniello, K. Ryder Wilkie, and R. Constantino. 2012. Associations of two ecologically significant social insect taxa in the litter of an amazonian rainforest: is there a relationship between ant and termite species richness? Psyche doi:10.1155/2012/312054
  • 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.
  • Silva T. S. R., and R. M. Feitosa. 2019. Using controlled vocabularies in anatomical terminology: A case study with Strumigenys (Hymenoptera: Formicidae). Arthropod Structure and Development 52: 1-26.
  • Sosa-Calvo J., S. O. Shattuck, and T. R. Schultz. 2006. Dacetine ants of Panama: new records and description of a new species. Proceedings of the Entomological Society of Washington 108: 814-821.
  • Sosa-Calvo J., T. R. Schultz, and J. S. LaPolla. 2010. A review of the dacetine ants of Guyana (Formicidae: Myrmicinae). Journal of Hymenoptera Research 19: 12-43.
  • Vasconcelos, H.L., J.M.S. Vilhena, W.E. Magnusson and A.L.K.M. Albernaz. 2006. Long-term effects of forest fragmentation on Amazonian ant communities. Journal of Biogeography 33:1348-1356
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