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The rarely collected myrmicine ant genus Rogeria has a disjunct distribution, with 37 species known to occur in the New World and 3 species that are known from the Australasian region (Kugler 1994). Rogeria ants are cryptic in habit and specimens are primarily collected from leaf litter and rotten wood, usually through Berlese or Winkler sampling. Not much is known about their biology, except that nests have been taken in rotting logs, under rocks, and from the trunks of cacao trees (Kugler 1994, LaPolla, J. S. and J. Sosa-Calvo, 2006).


Kugler (1994) - Monomorphic myrmicines. Antenna 12-segmented; scape not reaching posterior margin of head; distinct 3-segmented club longer than rest of funiculus; apical antennomere longer than combined lengths of other two club segments. No antennal scrobes or fossae. Clypeus projects narrowly between frontal lobes at least to posterior edge of antennal insertions. Body of clypeus with one or more pair of longitudinal carinulae. Lateral clypeus not raised into a ridge in front of antennal insertions. Nuchal grooves present on posteroventral corners of head. Anteroventral corners of pronotum angular to dentate and fitting into nuchal grooves. Propodeal spiracle 3 diameters or less from the edge of the propodeum below the propodeal spines. Metapleural lobes not sharply pointed.

Some members of Temnothorax have antennae like Rogeria and some have a narrow posterior lobe of the clypeus, but these have rounded anteroventral corners of the pronotum and no nuchal grooves. Of 65 species of Temnothorax examined at the Museum of Comparative Zoology, only one had an angular inferior corner of the pronotum, but in that species the scapes extend beyond the head, the posterior lobe of the clypeus is wider, and nuchal grooves are absent.

Some species of Lordomyrma, a genus sometimes confused with Rogeria in pacific islands, have similar antennal and clypeal features, but have a rounded anteroventral corner of the pronotum and lack nuchal grooves.

Stenamma workers are similar in form of clypeus, including narrow posterior portion between frontal lobes, and some have 3-segmented antennal clubs, but in that case the apical segment is shorter than the combined length of the other two segments. Also, Stenamma has no nuchal grooves, the anteroventral corner of the pronotum is rounded, and the metanotal groove is generally more distinct than in Rogeria species.

A number of Rogeria are highly variable and species level identification may be difficult for any particular collection or specimens.

Kugler (1994) organized species into groups (Rogeria species groups), stating "Some species can be assembled into more or less distinct species groups. Others can not be placed easily in any group, or seem to link several groups. These incertae sedis species are described with the group to which they may be most related." The diagnostic characters of these groups can be helpful in making species determinations.

Keys including this Genus


Keys to Species in this Genus


Kugler (1994) - Members of the genus Rogeria are distributed from Buenos Aires to southern Texas and Arizona, and in the Pacific between 10°N and 25°S from Tahiti to the western end of the island of New Guinea. So far it is unknown in Australia or southeastern United States. In the North American region, most species occur below the Isthmus of Tehuantepec, but two species (Rogeria creightoni, Rogeria cuneola) extend northward through the eastern lowlands of Mexico. Only Rogeria foreli and Rogeria creightoni have been collected in the United States. The North American region contains 8-10 endemic species (depending on the uncertain distributions of Rogeria innotabilis and Rogeria leptonana); the Caribbean, two endemic species; South America (including Trinidad), 19 endemic species and the Pacific, three endemic species. Only 5-7 species (depending on Rogeria innotabilis and Rogeria leptonana) are found in both Central America and northern South America.

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 1 3 0 2 38 0 0
Total Species 2841 1736 3045 932 835 4379 1741 2862


Kugler (1994) provided the following summary: Little is known of the biology of these cryptic ants. Collection records usually range from sea level to 1000m, but five species extend higher and two (Rogeria unguispina and Rogeria merenbergiana) can be found at 2000m. Rogeria species are generally collected in moist forests (primary or secondary forests, coffee or cacao plantations), but at higher elevations can be found in pastures (Rogeria leptonana, Rogeria merenbergiana). Several species (Rogeria creightoni, Rogeria cuneola, Rogeria foreli) have been found in both moist and dry climates. Rogeria foreli is the most unusual, with some members dwelling at over 1800m in the temperate mountains of southern Arizona.

Most Rogeria species have only been collected as strays or by Berlese or Winkler sampling, usually in leaf litter and rotten wood, but occasionally among epiphytes and moss (Rogeria belti, creightoni, Rogeria exsulans). Nests of several species (belti, Rogeria blanda, merenbergiana) have been found under loose bark of rotten logs. Nests of blanda and Rogeria tonduzi have been taken from the trunks of cacao trees. A nest of Rogeria leptonana was found at 1750m under a rock in a pasture.

Because nests are so rarely found, males are known for only four species (belti, blanda, leptonana and Rogeria stigmatica), and queens associated through nest series for only nine species.

Life History Traits

  • Mean colony size: 107 (Greer et al., 2021)
  • Compound colony type: not parasitic (Greer et al., 2021)
  • Nest site: hypogaeic; arboreal (Greer et al., 2021)
  • Diet class: omnivore (Greer et al., 2021)
  • Foraging stratum: subterranean/leaf litter; arboreal (Greer et al., 2021)



Worker Morphology

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• Antennal segment count: 12 • Antennal club: 3 • Palp formula: 3,3; 3,2; 2,2; 2,1 • Total dental count: 4-9 • Spur formula: 0, 0 • Eyes: 11-100 ommatidia • Pronotal Spines: absent • Mesonotal Spines: absent • Propodeal Spines: dentiform; present • Petiolar Spines: absent • Caste: none or weak • Sting: present • Metaplural Gland: present • Cocoon: absent

Male Morphology

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 • Antennal segment count 13 • Antennal club 0-gradual • Total dental count 4-5 • Spur formula 0, 0



Ochetomyrmex  (2 species, 0 fossil species)

Tranopelta  (2 species, 0 fossil species)

Diaphoromyrma  (1 species, 0 fossil species)

Lachnomyrmex  (16 species, 0 fossil species)

Blepharidatta  (4 species, 0 fossil species)

Allomerus  (8 species, 0 fossil species)

Wasmannia  (11 species, 0 fossil species)

Pheidole  (1,294 species, 7 fossil species)

Cephalotes  (123 species, 16 fossil species)

Procryptocerus  (44 species, 0 fossil species)

Strumigenys  (879 species, 4 fossil species)

Phalacromyrmex  (1 species, 0 fossil species)

Pilotrochus  (1 species, 0 fossil species)

Protalaridris  (7 species, 0 fossil species)

Rhopalothrix  (19 species, 0 fossil species)

Basiceros  (9 species, 0 fossil species)

Octostruma  (35 species, 0 fossil species)

Eurhopalothrix  (54 species, 0 fossil species)

Talaridris  (1 species, 0 fossil species)

Acanthognathus  (7 species, 1 fossil species)

Daceton  (2 species, 0 fossil species)

Lenomyrmex  (7 species, 0 fossil species)

Microdaceton  (4 species, 0 fossil species)

Orectognathus  (29 species, 0 fossil species)

Colobostruma  (16 species, 0 fossil species)

Epopostruma  (20 species, 0 fossil species)

Mesostruma  (9 species, 0 fossil species)


Apterostigma  (44 species, 2 fossil species)

Mycocepurus  (6 species, 0 fossil species)

Myrmicocrypta  (31 species, 0 fossil species)


Cyatta  (1 species, 0 fossil species)

Kalathomyrmex  (1 species, 0 fossil species)

Mycetarotes  (4 species, 0 fossil species)

Mycetosoritis  (2 species, 0 fossil species)

some Cyphomyrmex  (23 species, 2 fossil species)

some Cyphomyrmex

Paramycetophylax  (1 species, 0 fossil species)

Mycetophylax  (21 species, 0 fossil species)

Mycetagroicus  (4 species, 0 fossil species)

Mycetomoellerius  (31 species, 1 fossil species)

Sericomyrmex  (11 species, 0 fossil species)

Xerolitor  (1 species, 0 fossil species)

Paratrachymyrmex  (9 species, 0 fossil species)

Trachymyrmex  (9 species, 0 fossil species)

Amoimyrmex  (3 species, 0 fossil species)

Atta  (20 species, 1 fossil species)

some Acromyrmex  (56 species, 0 fossil species)

some Acromyrmex

Pseudoatta  (2 species, 0 fossil species)


Rostromyrmex  (1 species, 6 fossil species)

Cardiocondyla  (89 species, 0 fossil species)

Ocymyrmex  (34 species, 0 fossil species)

Nesomyrmex  (84 species, 2 fossil species)

Xenomyrmex  (5 species, 0 fossil species)

Terataner  (14 species, 0 fossil species)

Atopomyrmex  (3 species, 0 fossil species)

Cataulacus  (65 species, 3 fossil species)

Carebara  (249 species, 9 fossil species)

Diplomorium  (1 species, 0 fossil species)

Melissotarsus  (4 species, 1 fossil species)

Rhopalomastix  (14 species, 0 fossil species)

Calyptomyrmex  (38 species, 0 fossil species)

Strongylognathus  (27 species, 0 fossil species), Tetramorium  (598 species, 2 fossil species)

Cyphoidris  (4 species, 0 fossil species)

Dicroaspis  (2 species, 0 fossil species)

Aretidris  (2 species, 0 fossil species)

Vollenhovia  (83 species, 3 fossil species)

Dacetinops  (7 species, 0 fossil species)

Indomyrma  (2 species, 0 fossil species)

Crematogaster  (784 species, 3 fossil species)

Meranoplus  (91 species, 0 fossil species)

Lophomyrmex  (13 species, 0 fossil species)

Adlerzia  (1 species, 0 fossil species)

Recurvidris  (12 species, 0 fossil species)

Stereomyrmex  (3 species, 0 fossil species)

Trichomyrmex  (29 species, 0 fossil species)

Eutetramorium  (3 species, 0 fossil species)

Royidris  (15 species, 0 fossil species)

Malagidris  (6 species, 0 fossil species)

Vitsika  (16 species, 0 fossil species)

Huberia  (2 species, 0 fossil species)

Podomyrma  (62 species, 1 fossil species)

Liomyrmex  (1 species, 0 fossil species)

Metapone  (31 species, 0 fossil species)

Kartidris  (6 species, 0 fossil species)

Mayriella  (9 species, 0 fossil species)

Tetheamyrma  (2 species, 0 fossil species)

Dacatria  (1 species, 0 fossil species)

Proatta  (1 species, 0 fossil species)

Dilobocondyla  (22 species, 0 fossil species)

Secostruma  (1 species, 0 fossil species)

Acanthomyrmex  (19 species, 0 fossil species)

Myrmecina  (106 species, 0 fossil species)

Perissomyrmex  (6 species, 0 fossil species)

Pristomyrmex  (61 species, 3 fossil species)

some Lordomyrma  (36 species, 0 fossil species)

Propodilobus  (1 species, 0 fossil species)

Lasiomyrma  (4 species, 0 fossil species)

some Lordomyrma

Ancyridris  (2 species, 0 fossil species)

some Lordomyrma

Paratopula  (12 species, 0 fossil species)

Poecilomyrma  (2 species, 0 fossil species)

Romblonella  (10 species, 0 fossil species)

Rotastruma  (3 species, 0 fossil species)

Gauromyrmex  (3 species, 0 fossil species)

Vombisidris  (19 species, 0 fossil species)

Temnothorax  (512 species, 7 fossil species)

Harpagoxenus  (4 species, 0 fossil species)

Formicoxenus  (8 species, 0 fossil species)

Leptothorax  (20 species, 0 fossil species)

See Phylogeny of Myrmicinae for details.


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

  • ROGERIA [Myrmicinae: Stenammini]
    • Rogeria Emery, 1894c: 188. Type-species: Rogeria curvipubens, by subsequent designation of Wheeler, W.M. 1911f: 172.
    • Rogeria senior synonym of Irogera: Kempf, 1965: 185; Kugler, C. 1994: 23.
  • IROGERA [junior synonym of Rogeria]
    • Irogera Emery, 1915i: 191 [as subgenus of Rogeria]. Type-species: Rogeria procera, by original designation.
    • Irogera raised to genus: Brown, 1953h: 4 (in text); Kempf, 1961d: 436.
    • Irogera junior synonym of Rogeria: Kempf, 1965: 185; Kugler, C. 1994: 23.



Kugler (1994) - Mandibles usually triangular. Except in some ciliosa and foreli, mandibles with 5-7 teeth (3 apical teeth decreasing in size basad, followed by 2-3 smaller basal teeth). Additional denticles may occur among basal teeth or any basal tooth may be replaced by a pair of denticles. Palpal formula usually 3,2 or 2,2, but 3,3 in some stigmatica-group, and 2,1 in the very tiny minima. Scape neither elbowed nor ridged at the base, nor with an apron around the peduncle. Clypeus in profile usually with a very narrow anterior apron. Body of clypeus rises near vertically in most species, but occasionally projecting beyond the clypeal apron. Frontal lobes narrow; but covering antennal insertions; at most feebly notched behind. Frontal triangle small, depressed slightly. Eyes with 1-100 facets; located on sides, in the anterior half of the head (excluding mandibles). Sides of head widest just behind the eyes, forming rounded corners with the posterior head, which is weakly concave to weakly convex in full face view.

Mesosoma generally compact, broad shouldered. Anterior face of pronotum rises nearly vertically from the neck and usually forms a distinct, rounded angle with the dorsal surface. Mesosoma dorsum without sutures; no mesonotal groove; metanotal groove absent to distinct. Anterior edge of propodeum often marked by a transverse carina. Propodeal spines absent to long. Metapleural lobes low carinae to rounded triangular. Legs not incrassate. No tibial spurs on middle or hind legs. Tarsal claws simple.

Petiolar peduncle with or without a ventral keel; inferior process dentate except in stigmatica group. Node unarmed; poorly to well differentiated from peduncle. Postpetiole with short peduncles and a low node that is broader than long. Terminal segments of gaster rotated ventrad in all but the stigmatica group.

All pygidia dissected have a pair of small pygidial gland reservoirs and/or paired microareolate patches present on anterior edge, except in the stigmatica group. Common features of the sting apparatus are: 1) medial connection of spiracular plate incompletely sclerotized, 2) gonostylus single-segmented, 3) dorsoterminal chaeta present, 4) at least one companion seta (except gibba), 5) each lancet with a single moderate to large valve, 6) sting bulb large, with arched sting base.

Mandibles usually predominantly smooth, with piligerous punctures and vestigial carinulae at insertions, but carinulae stronger and more extensive in some members of the stigmatica-group. In all but ciliosa, the body of the clypeus is smooth with a pair of carinulae extending from the frontal lobes and stopping short of the clypeal apron; these are sometimes accompanied laterally by 1-2 shorter, weaker carinulae. Lateral extremities of clypeus and adjacent cheeks with longitudinal carinulae. Frontal triangle smooth, except in ciliosa. If macrosculpture present, frontal lobes and mid dorsum with diverging longitudinal rugae; rest of body areolate, rugose, or occasionally carinate. Microsculpture when present usually microareolate, appearing granular or punctured at lower magnifications. Posterior face of propodeum smooth, except in gibba. Legs smooth and shiny. First segment of gaster smooth and shiny; less so in prominula, and minima. Pygidium and sometimes other terminal terga with microscopic areolate sculpture on exposed posterior surfaces; pygidium may also possess minute piligerous tubercles.

Short appressed or decumbent pilosity common, most dependably on legs (except blanda and procera) and antennae. Terminal segments of gaster with erect hair. No erect hair on laterodorsa of head (under sweep of scapes). Body of clypeus just above apron with pairs of erect hairs; members of stigmatica group each with an additional median hair.

Color from brownish yellow to black, with mandibles, antennae, and legs lighter. Most species also with a lighter triangle on clypeus, cheeks, and frontal area.


  • 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 383, Rogeria in Myrmicinae, Tetramoriini)
  • Bolton, B. 1994. Identification guide to the ant genera of the world. Cambridge, Mass.: Harvard University Press, 222 pp. (page 106, Rogeria in Myrmicinae, Stenammini)
  • Bolton, B. 2003. Synopsis and Classification of Formicidae. Mem. Am. Entomol. Inst. 71: 370pp (page 204, Rogeria in Myrmicinae, Stenammini)
  • 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.
  • 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).
  • 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).
  • Chapman, J. W.; Capco, S. R. 1951. Check list of the ants (Hymenoptera: Formicidae) of Asia. Monogr. Inst. Sci. Technol. Manila 1: 1-327 (page 111, Rogeria in Myrmicinae, Leptothoracini)
  • Dlussky, G. M.; Fedoseeva, E. B. 1988. Origin and early stages of evolution in ants. Pp. 70-144 in: Ponomarenko, A. G. (ed.) Cretaceous biocenotic crisis and insect evolution. Moskva: Nauka, 232 pp. (page 79, Rogeria in Myrmicinae, Leptothoracini)
  • Donisthorpe, H. 1943h. A list of the type-species of the genera and subgenera of the Formicidae. [concl.]. Ann. Mag. Nat. Hist. 11(10): 721-737 (page 724, Rogeria in Myrmicinae, Leptothoracini)
  • Emery, C. 1894d. Studi sulle formiche della fauna neotropica. VI-XVI. Bull. Soc. Entomol. Ital. 26: 137-241 (page 188, Rogeria as genus)
  • Emery, C. 1895l. Die Gattung Dorylus Fab. und die systematische Eintheilung der Formiciden. Zool. Jahrb. Abt. Syst. Geogr. Biol. Tiere 8: 685-778 (page 769, Rogeria in Myrmicinae, Myrmicini)
  • 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, Rogeria in Myrmicinae, Leptothoracini)
  • Emery, C. 1924f [1922]. Hymenoptera. Fam. Formicidae. Subfam. Myrmicinae. [concl.]. Genera Insectorum 174C: 207-397 (page 266, Rogeria in Myrmicinae, Leptothoracini)
  • 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).
  • Forel, A. 1899d. Formicidae. [part]. Biol. Cent.-Am. Hym. 3: 25-56 (page 53, Rogeria in Myrmicinae, Myrmicini)
  • Forel, A. 1917. Cadre synoptique actuel de la faune universelle des fourmis. Bull. Soc. Vaudoise Sci. Nat. 51: 229-253 (page 245, Rogeria in Myrmicinae, Leptothoracini)
  • Hölldobler, B.; Wilson, E. O. 1990. The ants. Cambridge, Mass.: Harvard University Press, xii + 732 pp. (page 16, Rogeria in Myrmicinae, Pheidolini)
  • Jaffe, K. 1993. El mundo de las hormigas. Baruta, Venezuela: Equinoccio (Ediciones de la Universidad Simón Bolívar), 188 pp. (page 11, Rogeria in Myrmicinae, Leptothoracini)
  • Kempf, W. W. 1963a. Additions to the Neotropical ant genus Rogeria Emery, with a key to the hitherto recorded South American species (Hym., Formicidae). Rev. Bras. Biol. 23: 189-196 (page 195, Key to Neotropical species)
  • Kempf, W. W. 1965. Nota preliminar sôbre algumas formigas neotrópicas, descritas por Frederick Smith (Hymenoptera, Formicidae). Rev. Bras. Biol. 25: 181-186 (page 185, Rogeria senior synonym of Irogera)
  • Kempf, W. W. 1972b. Catálogo abreviado das formigas da regia~o Neotropical. Stud. Entomol. 15: 3-344 (page 227, Rogeria in Myrmicinae, Leptothoracini)
  • Kugler, C. 1994. A revision of the ant genus Rogeria with description of the sting apparatus (Hymenoptera: Formicidae). J. Hym. Res. 3: 17-89 (page 23, , Rogeria senior synonym of Irogera; Rogeria in Myrmicinae, Leptothoracini)
  • Kusnezov, N. 1958a. La posición sistematica del género Rogeria, con descripción de una nueva especie. Acta Zool. Lilloana 15: 41-45 (page 44, Rogeria in Myrmicinae, Myrmicini)
  • Kusnezov, N. 1964 [1963]. Zoogeografía de las hormigas en Sudamérica. Acta Zool. Lilloana 19: 25-186 (page 57, Rogeria in Myrmicinae, Myrmicini)
  • Smith, D. R. 1979. Superfamily Formicoidea. Pp. 1323-1467 in: Krombein, K. V., Hurd, P. D., Smith, D. R., Burks, B. D. (eds.) Catalog of Hymenoptera in America north of Mexico. Volume 2. Apocrita (Aculeata). Washington, D.C.: Smithsonian Institution Pr (page 1391, Rogeria in Myrmicinae, Leptothoracini)
  • Wheeler, W. M. 1910b. Ants: their structure, development and behavior. New York: Columbia University Press, xxv + 663 pp. (page 139, Rogeria in Myrmicinae, Myrmicini)
  • Wheeler, W. M. 1911g. A list of the type species of the genera and subgenera of Formicidae. Ann. N. Y. Acad. Sci. 21: 157-175 (page 172, Type-species: Rogeria curvipubens, by subsequent designation)
  • Wheeler, W. M. 1922i. Ants of the American Museum Congo expedition. A contribution to the myrmecology of Africa. VII. Keys to the genera and subgenera of ants. Bull. Am. Mus. Nat. Hist. 45: 631-710 (page 664, Rogeria in Myrmicinae, Leptothoracini)